Reconsideration of the National Ambient Air Quality Standards for Particulate Matter, 5558-5719 [2023-00269]
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ENVIRONMENTAL PROTECTION
AGENCY
40 CFR Parts 50, 53, and 58
[EPA–HQ–OAR–2015–0072; FRL–8635–01–
OAR]
RIN 2060–AV52
Reconsideration of the National
Ambient Air Quality Standards for
Particulate Matter
Environmental Protection
Agency (EPA).
ACTION: Proposed rule.
AGENCY:
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Dr.
Lars Perlmutt, Health and
Environmental Impacts Division, Office
of Air Quality Planning and Standards,
U.S. Environmental Protection Agency,
Mail Code C539–04, Research Triangle
Park, NC 27711; telephone: (919) 541–
3037; fax: (919) 541–5315; email:
perlmutt.lars@epa.gov.
FOR FURTHER INFORMATION CONTACT:
Based on the Environmental
Protection Agency’s (EPA’s)
reconsideration of the air quality criteria
and the national ambient air quality
standards (NAAQS) for particulate
matter (PM), the EPA proposes to revise
the primary annual PM2.5 standard by
lowering the level. The Agency
proposes to retain the current primary
24-hour PM2.5 standard and the primary
24-hour PM10 standard. The Agency also
proposes not to change the secondary
24-hour PM2.5 standard, secondary
annual PM2.5 standard, and secondary
24-hour PM10 standard at this time. The
EPA also proposes revisions to other key
aspects related to the PM NAAQS,
including revisions to the Air Quality
Index (AQI) and monitoring
requirements for the PM NAAQS.
DATES: Comments must be received on
or before March 28, 2023.
Public Hearings: The EPA will hold a
virtual public hearing on this proposed
rule. This hearing will be announced in
a separate Federal Register document
that provides details, including specific
dates, times, and contact information for
these hearings.
ADDRESSES: You may submit comments,
identified by Docket ID No. EPA–HQ–
OAR–2015–0072, by any of the
following means:
• Federal eRulemaking Portal:
https://www.regulations.gov/ (our
preferred method). Follow the online
instructions for submitting comments.
• Email: a-and-r-Docket@epa.gov.
Include the Docket ID No. EPA–HQ–
OAR–2015–0072 in the subject line of
the message.
• Mail: U.S. Environmental
Protection Agency, EPA Docket Center,
Air and Radiation Docket, Mail Code
28221T, 1200 Pennsylvania Avenue
NW, Washington, DC 20460.
• Hand Delivery or Courier (by
scheduled appointment only): EPA
Docket Center, WJC West Building,
Room 3334, 1301 Constitution Avenue
NW, Washington, DC 20004. The Docket
Center’s hours of operations are 8:30
SUMMARY:
a.m.–4:30 p.m., Monday–Friday (except
Federal Holidays).
Instructions: All submissions received
must include the Docket ID No. for this
document. Comments received may be
posted without change to https://
www.regulations.gov, including any
personal information provided. For
detailed instructions on sending
comments and additional information
on the rulemaking process, see the
SUPPLEMENTARY INFORMATION section of
this document.
SUPPLEMENTARY INFORMATION:
General Information
Preparing Comments for the EPA
Follow the online instructions for
submitting comments. Once submitted
to the Federal eRulemaking Portal,
comments cannot be edited or
withdrawn. The EPA may publish any
comment received to its public docket.
Do not submit electronically any
information you consider to be
Confidential Business Information (CBI)
or other information whose disclosure is
restricted by statute. Multimedia
submissions (audio, video, etc.) must be
accompanied by a written submission.
The written comment is considered the
official comment and should include
discussion of all points you wish to
make. The EPA will generally not
consider comments or comment
contents located outside of the primary
submission (i.e., on the web, the cloud,
or other file sharing system). For
additional submission methods, the full
EPA public comment policy,
information about CBI or multimedia
submissions, and general guidance on
making effective comments, please visit
https://www.epa.gov/dockets/
commenting-epa-dockets.
When submitting comments,
remember to:
• Identify the action by docket
number and other identifying
information (subject heading, Federal
Register date and page number).
• Explain why you agree or disagree,
suggest alternatives, and substitute
language for your requested changes.
• Describe any assumptions and
provide any technical information and/
or data that you used.
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• Provide specific examples to
illustrate your concerns and suggest
alternatives.
• Explain your views as clearly as
possible, avoiding the use of profanity
or personal threats.
• Make sure to submit your
comments by the comment period
deadline identified.
Availability of Information Related to
This Action
All documents in the dockets
pertaining to this action are listed on the
www.regulations.gov website. This
includes documents in the docket for
the proposed decision (Docket ID No.
EPA–HQ–OAR–2015–0072) and a
separate docket, established for the
Integrated Science Assessment (ISA)
(Docket ID No. EPA–HQ–ORD–2014–
0859) that has been adopted by
reference into the docket for this
proposed decision. Although listed in
the index, some information is not
publicly available, e.g., CBI or other
information whose disclosure is
restricted by statute. Certain other
material, such as copyrighted material,
is not placed on the internet and may be
viewed with prior arrangement with the
EPA Docket Center. Additionally, a
number of the documents that are
relevant to this proposed decision are
available through the EPA’s website at
https://www.epa.gov/naaqs/particulatematter-pm-air-quality-standards. These
documents include the Integrated
Science Assessment for Particulate
Matter (U.S. EPA, 2019a), available at
https://cfpub.epa.gov/ncea/isa/recor
display.cfm?deid=347534, the
Supplement to the 2019 Integrated
Science Assessment for Particulate
Matter (U.S. EPA, 2022a), available at
https://cfpub.epa.gov/ncea/isa/recor
display.cfm?deid=354490, and the
Policy Assessment for the
Reconsideration of the National
Ambient Air Quality Standards for
Particulate Matter (U.S. EPA, 2022b),
available at https://www.epa.gov/naaqs/
particulate-matter-pm-standardsintegrated-science-assessments-currentreview.
Table of Contents
The following topics are discussed in
this preamble:
Executive Summary
I. Background
A. Legislative Requirements
B. Related PM Control Programs
C. Review of the Air Quality Criteria and
Standards for Particulate Matter
1. Reviews Completed in 1971 and 1987
2. Review Completed in 1997
3. Review Completed in 2006
4. Review Completed in 2012
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5. Review Completed in 2020
6. Reconsideration of the 2020 PM NAAQS
Final Action
a. Decision To Initiate a Reconsideration
b. Process for Reconsideration of the 2020
PM NAAQS Decision
D. Air Quality Information
1. Distribution of Particle Size in Ambient
Air
2. Sources and Emissions Contributing to
PM in the Ambient Air
3. Monitoring of Ambient PM
4. Ambient Concentrations and Trends
a. PM2.5 Mass
b. PM2.5 Components
c. PM10
d. PM10–2.5
e. UFP
5. Characterizing Ambient PM2.5
Concentrations for Exposure
a. Predicted Ambient PM2.5 and Exposure
Based on Monitored Data
b. Comparison of PM2.5 Fields in
Estimating Exposure and Relative to
Design Values
6. Background PM
II. Rationale for Proposed Decisions on the
Primary PM2.5 Standards
A. General Approach
1. Background on the Current Standards
a. Considerations Regarding the Adequacy
of the Existing Standards in the 2020
Review
2. General Approach and Key Issues in
This Reconsideration of the 2020 Final
Decision
B. Overview of the Health Effects Evidence
1. Nature of Effects
a. Mortality
b. Cardiovascular Effects
c. Respiratory Effects
d. Cancer
e. Nervous System Effects
f. Other Effects
2. Public Health Implications and At-Risk
Populations
3. PM2.5 Concentrations in Key Studies
Reporting Health Effects
a. PM2.5 Exposure Concentrations
Evaluated in Experimental Studies
b. Ambient PM2.5 Concentrations in
Locations of Epidemiologic Studies
4. Uncertainties in the Health Effects
Evidence
C. Summary of Exposure and Risk
Estimates
1. Key Design Aspects
2. Key Limitations and Uncertainties
3. Summary of Risk Estimates
D. Proposed Conclusions on the Primary
PM2.5 Standards
1. CASAC Advice in This Reconsideration
2. Evidence- and Risk-Based
Considerations in the Policy Assessment
a. Evidence-Based Considerations
b. Risk-Based Considerations
3. Administrator’s Proposed Conclusions
on the Primary PM2.5 Standards
a. Adequacy of the Current Primary PM2.5
Standards
b. Consideration of Alternative Primary
Annual PM2.5 Standard Levels
E. Proposed Decisions on the Primary
PM2.5 Standards
III. Rationale for Proposed Decisions on the
Primary PM10 Standard
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A. General Approach
1. Background on the Current Standard
i. Considerations Regarding the Adequacy
of the Existing Standard in the 2020
Review
2. General Approach and Key Issues in
This Reconsideration of the 2020 Final
Decision
B. Overview of Health Effects Evidence
1. Nature of Effects
a. Mortality
i. Long-Term Exposures
ii. Short-Term Exposures
b. Cardiovascular Effects
i. Long-Term Exposures
ii. Short-Term Exposures
c. Respiratory Effects—Short-Term
Exposures
d. Cancer—Long-Term Exposures
e. Metabolic Effects—Long-Term Exposures
f. Nervous System Effects—Long-Term
Exposures
C. Proposed Conclusions on the Primary
PM10 Standard
1. CASAC Advice in This Reconsideration
2. Evidence-Based Considerations in the
Policy Assessment
3. Administrator’s Proposed Decision on
the Current Primary PM10 Standard
IV. Communication of Public Health
A. Air Quality Index Overview
B. Air Quality Index Category Breakpoints
for PM2.5
1. Air Quality Index Values of 50, 100 and
150
2. Air Quality Index Values of 200 and 300
3. Air Quality Index Value of 500
C. Air Quality Index Category Breakpoints
for PM10
D. Air Quality Index Reporting
V. Rationale for Proposed Decisions on the
Secondary PM Standards
A. General Approach
1. Background on the Current Standards
a. Non-Visibility Effects
i. Considerations Regarding Adequacy of
the Existing Standards for Non-Visibility
Effects in the 2020 Review
b. Visibility Effects
i. Considerations Regarding Adequacy of
the Existing Standards for Visibility
Effects in the 2020 Review
2. General Approach and Key Issues in
This Reconsideration of the 2020 Final
Decision
B. Overview of Welfare Effects Evidence
1. Nature of Effects
a. Visibility
b. Climate
c. Materials
C. Summary of Air Quality and
Quantitative Information
1. Visibility Effects
a. Target Level of Protection in Terms of a
PM2.5 Visibility Index
b. Relationship Between the PM2.5
Visibility Index and the Current
Secondary 24-Hour PM2.5 Standard
2. Non-Visibility Effects
D. Proposed Conclusions on the Secondary
PM Standards
1. CASAC Advice in This Reconsideration
2. Evidence- and Quantitative InformationBased Considerations in the Policy
Assessment
3. Administrator’s Proposed Decision on
the Current Secondary PM Standards
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VI. Interpretation of the NAAQS for PM
A. Proposed Amendments to Appendix K:
Interpretation of the NAAQS for
Particulate Matter
1. Updating Design Value Calculations To
Be on a Site-Level Basis
2. Codifying Site Combinations To
Maintain a Continuous Data Record
3. Clarifying Daily Validity Requirements
for Continuous Monitors
B. Proposed Amendments to Appendix N:
Interpretation of the NAAQS for PM2.5
1. Updating References to the Proposed
Revision(s) of the Standards
2. Codifying Site Combinations To
Maintain a Continuous Data Record
VII. Proposed Amendments to Ambient
Monitoring and Quality Assurance
Requirements
A. Proposed Amendment in 40 CFR Part 50
(Appendix L): Reference Method for the
Determination of Fine Particulate Matter
as PM2.5 in the Atmosphere—Addition of
the Tisch Cyclone as an Approved
Second Stage Separator
B. Issues Related to 40 CFR Part 53
(Reference and Equivalent Methods)
1. Update to Program Title and Delivery
Address for FRM and FEM Application
and Modification Requests
2. Requests for Delivery of a Candidate
FRM or FEM Instrument
3. Amendments to Requirements for
Submission of Materials in § 53.4(b)(7)
for Language and Format
4. Amendment to Designation of Reference
and Equivalent Methods
5. Amendment to One Test Field Campaign
Requirement for Class III PM2.5 FEMs
6. Amendment to Use of Monodisperse
Aerosol Generator
7. Corrections to 40 CFR Part 53 (Reference
and Equivalent Methods)
C. Proposed Changes to 40 CFR Part 58
(Ambient Air Quality Surveillance)
1. Quality Assurance Requirements for
Monitors Used in Evaluations for
National Ambient Air Quality Standards
a. Quality System Requirements
b. Measurement Quality Check
Requirements
c. Calculations for Data Quality
Assessments
d. References
2. Quality Assurance Requirements for
Prevention of Significant Deterioration
(PSD) Air Monitoring
a. Quality System Requirements
b. Measurement Quality Check
Requirements
c. Calculations for Data Quality
Assessments
d. References
3. Proposed Amendments to PM Ambient
Air Quality Methodology
a. Proposal To Revoke Approved Regional
Methods (ARMs)
b. Proposal for Calibration of PM Federal
Equivalent Methods (FEMs)
4. Proposed Amendment to the PM2.5
Monitoring Network Design Criteria To
Address At-Risk Communities
5. Proposed Revisions To Probe and
Monitoring Path Siting Criteria
a. Providing Separate Section for Open
Path Monitoring Requirements
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b. Amending Distance Precision for
Spacing Offsets
c. Clarifying Summary Table of Probe
Siting Criteria
d. Adding Flexibility for the Spacing From
Minor Sources
e. Amendments and Clarification for the
Spacing From Obstructions and Trees
f. Reinstating Minimum 270-Degree Arc
and Clarifying 180-Degree Arc in
Regulatory Text
g. Clarification on Obstacles That Act as an
Obstruction
h. Amending and Clarifying the 10-Meter
Tree Dripline Requirement
i. Amending Spacing Requirement for
Microscale Monitoring
j. Amending Waiver Provisions
k. Broadening of Acceptable Probe
Materials
D. Taking Comment on Incorporating Data
From Next Generation Technologies
1. Background on Use of FRM and FEM
Monitors
2. Next Generation Technologies: Data
Considerations
3. PM2.5 Continuous FEMs
4. PM2.5 Satellite Products
5. Use of Air Sensors
6. Summary
VIII. Clean Air Act Implementation
Requirements for the PM NAAQS
A. Designation of Areas
B. Section 110(a)(1) and (2) Infrastructure
SIP Requirements
C. Implementing Any Revised PM2.5
NAAQS in Nonattainment Areas
D. Implementing the Primary and
Secondary PM10 NAAQS
E. Prevention of Significant Deterioration
and Nonattainment New Source Review
Programs for the Proposed Revised
Primary Annual PM2.5 NAAQS
F. Transportation Conformity Program
G. General Conformity Program
IX. Statutory and Executive Order Reviews
A. Executive Order 12866: Regulatory
Planning and Review and Executive
Order 13563: Improving Regulation and
Regulatory Review
B. Paperwork Reduction Act (PRA)
C. Regulatory Flexibility Act (RFA)
D. Unfunded Mandates Reform Act
(UMRA)
E. Executive Order 13132: Federalism
F. Executive Order 13175: Consultation
and Coordination With Indian Tribal
Governments
G. Executive Order 13045: Protection of
Children From Environmental Health
and Safety Risks
H. Executive Order 13211: Actions
Concerning Regulations That
Significantly Affect Energy Supply,
Distribution or Use
I. National Technology Transfer and
Advancement Act (NTTAA)
J. Executive Order 12898: Federal Actions
To Address Environmental Justice in
Minority Populations and Low-Income
Populations
References
Executive Summary
This document presents the
Administrator’s proposed decisions for
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the reconsideration of the 2020 final
decision on the primary (health-based)
and secondary (welfare-based) National
Ambient Air Quality Standards
(NAAQS) for Particulate Matter (PM).
More specifically this document
summarizes the background and
rationale for the Administrator’s
proposed decisions to revise the
primary annual PM2.5 standard by
lowering the level from 12.0 mg/m3 to
within the range of 9.0 to 10.0 mg/m3
while taking comment on alternative
annual standard levels down to 8.0 mg/
m3 and up to 11.0 mg/m3; to retain the
current primary 24-hour PM2.5 standard
(at a level of 35 mg/m3) while taking
comment on revising the level as low as
25 mg/m3; to retain the primary 24-hour
PM10 standard, without revision; and,
not to change the secondary PM
standards at this time, while taking
comment on revising the level of the
secondary 24-hour PM2.5 standard as
low as 25 mg/m3. In reaching his
proposed decisions, the Administrator
has considered the currently available
scientific evidence in the 2019
Integrated Science Assessment (2019
ISA) and the Supplement to the 2019
ISA (ISA Supplement), quantitative and
policy analyses presented in the Policy
Assessment (PA), and advice from the
Clean Air Scientific Advisory
Committee (CASAC). The EPA solicits
comment on the proposed decisions
described here and on the array of
issues associated with the
reconsideration of these standards,
including the judgments of public
health, public welfare and science
policy inherent in the proposed
decisions, and requests commenters also
provide the rationales upon which
views articulated in submitted
comments are based.
The EPA has established primary and
secondary standards for PM2.5, which
includes particles with diameters
generally less than or equal to 2.5 mm,
and PM10, which includes particles with
diameters generally less than or equal to
10 mm. The standards include two
primary PM2.5 standards, an annual
average standard, averaged over three
years, with a level of 12.0 mg/m3 and a
24-hour standard with a 98th percentile
form, averaged over three years, and a
level of 35 mg/m3. It also includes a
primary PM10 standard with a 24-hour
averaging time, and a level of 150 mg/
m3, not to be exceeded more than once
per year on average over three years.
Secondary PM standards are set equal to
the primary standards, except that the
level of the secondary annual PM2.5
standard is 15.0 mg/m3.
The last review of the PM NAAQS
was completed in December 2020. In
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that review, the EPA retained the
primary and secondary NAAQS,
without revision (85 FR 82684,
December 18, 2020). Following
publication of the 2020 final action,
several parties filed petitions for review
and petitions for reconsideration of the
EPA’s final decision.
In June 2021, the Agency announced
its decision to reconsider the 2020 PM
NAAQS final action.1 The EPA is
reconsidering the December 2020
decision because the available scientific
evidence and technical information
indicate that the current standards may
not be adequate to protect public health
and welfare, as required by the Clean
Air Act. The EPA noted that the 2020
PA concluded that the scientific
evidence and information called into
question the adequacy of the primary
PM2.5 standards and supported
consideration of revising the level of the
primary annual PM2.5 standard to below
the current level of 12.0 mg/m3 while
retaining the primary 24-hour PM2.5
standard (U.S. EPA, 2020a). The EPA
also noted that the 2020 PA concluded
that the available scientific evidence
and information did not call into
question the adequacy of the primary
PM10 or secondary PM standards and
supported consideration of retaining the
primary PM10 standard and secondary
PM standards without revision (U.S.
EPA, 2020a).
The proposed decisions presented in
this document on the primary PM2.5
standards have been informed by key
aspects of the available health effects
evidence and conclusions contained in
the 2019 ISA and ISA Supplement,
quantitative exposure/risk analyses and
policy evaluations presented in the PA,
advice from the CASAC 2 and public
comment received as part of this
reconsideration.3 The health effects
evidence available in this
reconsideration, in conjunction with the
full body of evidence critically
evaluated in the 2019 ISA, supports a
causal relationship between long- and
1 The press release for this announcement is
available at: https://www.epa.gov/newsreleases/epareexamine-health-standards-harmful-soot-previousadministration-left-unchanged.
2 In 2021, the Administrator announced his
decision to reestablish the membership of the
CASAC. The Administrator selected seven members
to serve on the chartered CASAC, and appointed a
PM CASAC panel to support the chartered CASAC’s
review of the draft ISA Supplement and the draft
PA as a part of this reconsideration (see section
I.C.6.b below for more information).
3 More information regarding the CASAC review
of the draft ISA Supplement and the draft PA,
including opportunities for public comment, can be
found in the following Federal Register notices: 86
FR 54186, September 30, 2021; 86 FR 52673,
September 22, 2021; 86 FR 56263, October 8, 2021;
87 FR 958, January 7, 2022.
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short-term exposures and mortality and
cardiovascular effects, and the evidence
supports a likely to be a causal
relationship between long-term
exposures and respiratory effects,
nervous system effects, and cancer. The
longstanding evidence base, including
animal toxicological studies, controlled
human exposure studies, and
epidemiologic studies, reaffirms, and in
some cases strengthens, the conclusions
from past reviews regarding the health
effects of PM2.5 exposures.
Epidemiologic studies available in this
reconsideration demonstrate generally
positive, and often statistically
significant, PM2.5 health effect
associations. Such studies report
associations between estimated PM2.5
exposures and non-accidental,
cardiovascular, or respiratory mortality;
cardiovascular or respiratory
hospitalizations or emergency room
visits; and other mortality/morbidity
outcomes (e.g., lung cancer mortality or
incidence, asthma development). The
scientific evidence available in this
reconsideration, as evaluated in the
2019 ISA and ISA Supplement, includes
a number of epidemiologic studies that
use various methods to characterize
exposure to PM2.5 (e.g., ground-based
monitors and hybrid modeling
approaches) and to evaluate associations
between health effects and lower
ambient PM2.5 concentrations. There are
a number of recent epidemiologic
studies that use varying study designs
that reduce uncertainties related to
confounding and exposure
measurement error. The results of these
analyses provide further support for the
robustness of associations between
PM2.5 exposures and mortality and
morbidity. Moreover, the Administrator
notes that recent epidemiologic studies
strengthen support for health effect
associations at lower PM2.5
concentrations, with these new studies
finding positive and significant
associations when assessing exposure in
locations and time periods with lower
mean and 25th percentile
concentrations than those evaluated in
epidemiologic studies available at the
time of previous reviews. Additionally,
the experimental evidence (i.e., animal
toxicological and controlled human
exposure studies) strengthens the
coherence of effects across scientific
disciplines and provides additional
support for potential biological
pathways through which PM2.5
exposures could lead to the overt
population-level outcomes reported in
epidemiologic studies for the health
effect categories for which a causal
relationship (i.e., short- and long-term
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PM2.5 exposure and mortality and
cardiovascular effects) or likely to be
causal relationship (i.e., short- and longterm PM2.5 exposure and respiratory
effects; and long-term PM2.5 exposure
and nervous system effects and cancer)
was concluded.
The available evidence in the 2019
ISA continues to provide support for
factors that may contribute to increased
risk of PM2.5-related health effects
including lifestage (children and older
adults), pre-existing diseases
(cardiovascular disease and respiratory
disease), race/ethnicity, and
socioeconomic status. For example, the
2019 ISA and ISA Supplement conclude
that there is strong evidence that Black
and Hispanic populations, on average,
experience higher PM2.5 exposures and
PM2.5-related health risk than nonHispanic White populations. In
addition, studies evaluated in the 2019
ISA and ISA Supplement also provide
evidence indicating that communities
with lower socioeconomic status (SES),
as assessed in epidemiologic studies
using indicators of SES including
income and educational attainment are,
on average, exposed to higher
concentrations of PM2.5 compared to
higher SES communities.
The quantitative risk assessment, as
well as policy considerations in the PA,
also inform the proposed decisions on
the primary PM2.5 standards. The risk
assessment in this consideration focuses
on all-cause or nonaccidental mortality
associated with long- and short-term
PM2.5 exposures. The primary analyses
focus on exposure and risk associated
with air quality that might occur in an
area under air quality conditions that
just meet the current and potential
alternative standards. The risk
assessment estimates that the current
primary PM2.5 standards could allow a
substantial number of PM2.5-associated
premature deaths in the United States,
and that public health improvements
would be associated with just meeting
all of the alternative (more stringent)
annual and 24-hour standard levels
modeled. Additionally, the results of the
risk assessment suggest that for most of
the U.S., the annual standard is the
controlling standard and that revision to
that standard has the most potential to
reduce PM2.5 exposure related risk.
Further analyses comparing the
reductions in average national PM2.5
concentrations and risk rates within
each demographic population estimate
that the average percent PM2.5
concentrations and risk reductions are
slightly greater in the Black population
than in the White population when
meeting a revised annual standard with
a lower level. The analyses are
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summarized in this document and
described in detail in the PA.
In its advice to the Administrator, the
CASAC concurred with the draft PA
that the currently available health
effects evidence calls into question the
adequacy of the primary annual PM2.5
standard. With regard to the primary
annual PM2.5 standard, the majority of
the CASAC concluded that the level of
the standard should be revised within
the range of 8.0 to 10.0 mg/m3, while the
minority of the CASAC concluded that
the primary annual PM2.5 standard
should be revised to a level of 10.0 to
11.0 mg/m3. With regard to the primary
24-hour PM2.5 standard, the majority of
the CASAC concluded that the primary
24-hour PM2.5 was not adequate and that
the level of the standard should be
revised to within the range of 25 to 30
mg/m3, while the minority of the CASAC
concluded that the primary 24-hour
PM2.5 standard was adequate and should
be retained, without revision.
In considering how to revise the suite
of standards to provide the requisite
degree of protection, the Administrator
recognizes that the current annual
standard and 24-hour standard,
together, are intended to provide public
health protection against the full
distribution of short- and long-term
PM2.5 exposures. Further, he recognizes
that changes in PM2.5 air quality
designed to meet either the annual or
the 24-hour standard would likely result
in changes to both long-term average
and short-term peak PM2.5
concentrations. Based on the current
evidence and quantitative information,
as well as consideration of CASAC
advice and public comment thus far in
this reconsideration, the Administrator
proposes to conclude that the current
primary PM2.5 standards are not
adequate to protect public health with
an adequate margin of safety.
The Administrator also notes that the
CASAC was unanimous in its advice
regarding the need to revise the annual
standard. In considering the appropriate
level for a revised annual standard, the
Administrator provisionally concludes
that a standard set within the range of
9.0 to 10.0 mg/m3 would reflect his
placing the most weight on the strongest
available evidence while appropriately
weighing the uncertainties. In addition,
the Administrator recognizes that some
members of CASAC advised, and the PA
concluded, that the available scientific
information provides support for
considering a range that extends up to
11.0 mg/m3 and down to 8.0 mg/m3.
With regard to the primary 24-hour
PM2.5 standard, the Administrator finds
it is less clear whether the available
scientific evidence and quantitative
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information calls into question the
adequacy of the public health protection
afforded by the current 24-hour
standard. He notes that a more stringent
annual standard is expected to reduce
both average (annual) concentrations
and peak (daily) concentrations.
Furthermore, he notes that the CASAC
did not reach consensus on whether
revisions to the primary 24-hour PM2.5
standard were warranted at this time.
The majority of the CASAC
recommended that the level of the
current primary 24-hour PM2.5 should
be revised to within the range of 25 to
30 mg/m3, while the minority of the
CASAC recommended retaining the
current standard. The Administrator
proposes to conclude that the 24-hour
standard should be retained,
particularly when considered in
conjunction with the protection
provided by the suite of standards and
the proposed decision to revise the
annual standard to a level of 9.0 to 10.0
mg/m3.
The EPA solicits comment on the
Administrator’s proposed conclusions,
and on the proposed decision to revise
the primary annual PM2.5 standard and
retain the primary 24-hour PM2.5
standard, without revision. The
Administrator is conscious of his
obligation to set primary standards with
an adequate margin of safety and
preliminarily determines that the
proposed decision balances the need to
provide protection against uncertain
risks with the obligation to not set
standards that are more stringent than
necessary. The requirement to provide
an adequate margin of safety was
intended to address uncertainties
associated with inconclusive scientific
and technical information and to
provide a reasonable degree of
protection against hazards that research
has not yet identified. Reaching
decisions on what standards are
appropriate necessarily requires
judgments of the Administrator about
how to consider the information
available from the epidemiologic studies
and other relevant evidence. In the
Administrator’s judgment, the proposed
suite of primary PM2.5 standards reflects
the appropriate consideration of the
strength of the available evidence and
other information and their associated
uncertainties and the advice of the
CASAC. The final rulemaking will
reflect the Administrator’s ultimate
judgments as to the suite of primary
PM2.5 standards that are requisite to
protect the public health with an
adequate margin of safety. Consistent
with these principles, the EPA also
solicits public comment on alternative
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annual standard levels down to 8.0 mg/
m3 and up to 11.0 mg/m3, on an
alternative 24-hour standard level as
low as 25 mg/m3 and on the combination
of annual and 24-hour standards that
commenters may believe is appropriate,
along with the approaches and scientific
rationales used to support such levels.
For example, the EPA solicits comments
on the uncertainties in the reported
associations between daily or annual
average PM2.5 exposures and mortality
or morbidity in the epidemiologic
studies, the significance of the 25th
percentile of ambient concentrations
reported in studies, the relevance and
limitations of international studies, and
other topics discussed in section
II.D.3.b.
The primary PM10 standard is
intended to provide public health
protection against health effects related
to exposures to PM10–2.5, which are
particles with a diameter between 10 mm
and 2.5 mm. The proposed decision to
retain the current 24-hour PM10
standard has been informed by key
aspects of the available health effects
evidence and conclusions contained in
the 2019 ISA, the policy evaluations
presented in the PA, advice from the
CASAC and public comment received as
part of this reconsideration.
Specifically, the health effects evidence
for PM10–2.5 exposures is somewhat
strengthened since past reviews,
although the strongest evidence still
only provides support for a suggestive
of, but not sufficient to infer, causal
relationship with long- and short-term
exposures and mortality and
cardiovascular effects, short-term
exposures and respiratory effects, and
long-term exposures and cancer,
nervous system effects, and metabolic
effects. In reaching his proposed
decision, the Administrator recognizes
that, while the available health effects
evidence has expanded, recent studies
are subjected to the same types of
uncertainties that were judged to be
important in previous reviews. He also
recognizes that the CASAC generally
agreed with the draft PA that it was
reasonable to retain the primary 24-hour
PM10 standard given the available
scientific evidence, including PM10 as
an appropriate indicator. He proposes to
conclude that the newly available
evidence does not call into question the
adequacy of the current primary PM10
standard, and he proposes to retain that
standard, without revision.
This reconsideration of the secondary
PM standards focuses on visibility,
climate, and materials effects.4 The
4 Consistent with the 2016 Integrated Review Plan
(U.S. EPA, 2016), other welfare effects of PM, such
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Administrator’s proposed decision to
not change the current secondary
standards at this time has been informed
by key aspects of the currently available
welfare effects evidence as well as the
conclusions contained in the 2019 ISA
and ISA Supplement; quantitative
analyses of visibility impairment; policy
evaluations presented in the PA; advice
from the CASAC; and public comment
received as part of this reconsideration.
Specifically, the welfare effects
evidence available in this
reconsideration is consistent with the
evidence available in previous reviews
and supports a causal relationship
between PM and visibility, climate, and
materials effects. With regard to climate
and materials effects, while the
evidence has expanded since previous
reviews, uncertainties remain in the
evidence and there are still significant
limitations in quantifying potential
adverse effects from PM on climate and
materials for purposes of setting a
standard. With regard to visibility
effects, the results of quantitative
analyses of visibility impairment are
similar to those in previous reviews,
and suggest that in areas that meet the
current secondary 24-hour PM2.5
standard that estimated light extinction
in terms of a 3-year visibility metric
would be at or well below the upper end
of the range for the target level of
protection (i.e., 30 deciviews (dv)). The
CASAC generally agreed with the draft
PA that substantial uncertainties remain
in the scientific evidence for climate
and materials effects. In considering the
available scientific evidence for climate
and materials effects, along with CASAC
advice, the Administrator proposes to
conclude that it is appropriate to retain
the existing secondary standards and
that it is not appropriate to establish any
distinct secondary PM standards to
address non-visibility PM-related
welfare effects. With regard to visibility
effects, while the Administrator notes
that the CASAC did not recommend
revising either the target level of
protection for the visibility index or the
level of the current secondary 24-hour
PM2.5 standard, the Administrator
as ecological effects, are being considered in the
separate, on-going review of the secondary NAAQS
for oxides of nitrogen, oxides of sulfur and PM.
Accordingly, the public welfare protection provided
by the secondary PM standards against ecological
effects such as those related to deposition of
nitrogen- and sulfur-containing compounds in
vulnerable ecosystems is being considered in that
separate review. Thus, the Administrator’s
conclusion in this reconsideration of the 2020 final
decision will be focused only and specifically on
the adequacy of public welfare protection provided
by the secondary PM standards from effects related
to visibility, climate, and materials and hereafter
‘‘welfare effects’’ refers to those welfare effects.
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recognizes that, should an alternative
level be considered for the visibility
index, that the CASAC recommends
also considering revisions to the
secondary 24-hour PM2.5 standard. In
considering the available evidence and
quantitative information, with its
inherent uncertainties and limitations,
the Administrator proposes not to
change the secondary PM standards at
this time, and solicits comment on this
proposed decision. In addition, the
Administrator additionally solicits
comment on the appropriateness of a
target level of protection for visibility
below 30 dv and down as low as 25 dv,
and of revising the level of the current
secondary 24-hour PM2.5 standard to a
level as low as 25 mg/m3.
Any proposed revisions to the PM
NAAQS, if finalized, would trigger a
process under which states (and tribes,
if they choose) make recommendations
to the Administrator regarding
designations, identifying areas of the
country that either meet or do not meet
the new or revised PM NAAQS. Those
areas that do not meet the PM NAAQS
will need to develop plans that
demonstrate how they will meet the
standards. As part of these plans, states
have the opportunity to use tools to
advance environmental justice, in this
case for overburdened communities in
areas with high PM concentrations
above the NAAQS, as provided in
current PM NAAQS implementation
guidance to meet requirements (80 FR
58010, 58136, August 25, 2016). The
EPA is not proposing changes to any of
the current PM NAAQS implementation
programs in this proposed rulemaking,
and therefore is not requesting comment
on any specific proposals related to
implementation or designations.
On other topics, the EPA proposes to
make two sets of changes to the PM2.5
sub-index of the AQI. First, the EPA
proposes to continue to use the
approach used in the revisions to the
AQI in 2012 (77 FR 38890, June 29,
2012) of setting the lower breakpoints
(50, 100 and 150) to be consistent with
the levels of the primary PM2.5 annual
and 24-hour standards and proposes to
revise the lower breakpoints to be
consistent with any changes to the
primary PM2.5 standards that are part of
this reconsideration. In so doing, the
EPA proposes to revise the AQI value of
50 within the range of 9.0 and 10.0 mg/
m3 and proposes to retain the AQI
values of 100 and 150 at 35.4 mg/m3 and
55.4 mg/m3, respectively. Second, the
EPA proposes to revise the upper AQI
breakpoints (200 and above) and to
replace the linear-relationship approach
used in 1999 (64 FR 42530, August 4,
1999) to set these breakpoints, with an
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approach that more fully considers the
PM2.5 health effects evidence from
controlled human exposure and
epidemiologic studies that has become
available in the last 20 years. The EPA
also proposes to revise the AQI values
of 200, 300 and 500 to 125.4 mg/m3,
225.4 mg/m3, and 325.4 mg/m3,
respectively. The EPA proposes to
finalize these changes to the PM2.5 AQI
in conjunction with the Agency’s final
decisions on the primary annual and 24hour PM2.5 standards, if proposed
revisions to such standards are
promulgated. The EPA is soliciting
comment on the proposed revisions to
the AQI. In addition, the EPA also
proposes to revise the daily reporting
requirement from 5 days per week to 7
days per week, while also reformatting
appendix G and providing clarifications.
With regard to monitoring-related
activities, the EPA proposes revisions to
data calculations and ambient air
monitoring requirements for PM to
improve the usefulness of and
appropriateness of data used in
regulatory decision making and to better
characterize air quality in communities
that are at increased risk of PM2.5
exposure and health risk. These
proposed changes are found in 40 CFR
part 50 (appendices K, L, and N), part
53, and part 58 with associated
appendices (A, B, C, D, and E). These
proposed changes include addressing
updates in data calculations, approval of
reference and equivalent methods,
updates in quality assurance statistical
calculations to account for lower
concentration measurements, updates to
support improvements in PM methods,
a revision to the PM2.5 network design
to account for at-risk populations, and
updates to the Probe and Monitoring
Path Siting Criteria for NAAQS
pollutants.
In setting the NAAQS, the EPA may
not consider the costs of implementing
the standards. This was confirmed by
the Supreme Court in Whitman v.
American Trucking Associations, 531
U.S. 457, 465–472, 475–76 (2001), as
discussed in section II.A of this
document. As has traditionally been
done in NAAQS rulemaking, the EPA
prepared a Regulatory Impact Analysis
(RIA) to provide the public with
information on the potential costs and
benefits of attaining several alternative
PM2.5 standard levels. In NAAQS
rulemaking, the RIA is done for
informational purposes only, and the
proposed decisions on the NAAQS in
this rulemaking are not based on
consideration of the information or
analyses in the RIA. The RIA fulfills the
requirements of Executive Orders 13563
and 12866. The RIA estimates the costs
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5563
and monetized human health benefits of
attaining three alternative annual PM2.5
standard levels and one alternative 24hour PM2.5 standard level. Specifically,
the RIA examines the proposed annual
and 24-hour alternative standard levels
of 10/35 mg/m3 and 9/35 mg/m3, as well
as the following two more stringent
alternative standard levels: (1) An
alternative annual standard level of 8
mg/m3 in combination with the current
24-hour standard (i.e., 8/35 mg/m3), and
(2) an alternative 24-hour standard level
of 30 mg/m3 in combination with the
proposed annual standard level of 10
mg/m3 (i.e., 10/30 mg/m3). The RIA
presents estimates of the costs and
benefits of applying illustrative national
control strategies in 2032 after
implementing existing and expected
regulations and assessing emissions
reductions to meet the current annual
and 24-hour particulate matter NAAQS
(12/35 mg/m3).
I. Background
A. Legislative Requirements
Two sections of the Clean Air Act
(CAA) govern the establishment and
revision of the NAAQS. Section 108 (42
U.S.C. 7408) directs the Administrator
to identify and list certain air pollutants
and then to issue air quality criteria for
those pollutants. The Administrator is
to list those pollutants ‘‘emissions of
which, in his judgment, cause or
contribute to air pollution which may
reasonably be anticipated to endanger
public health or welfare’’; ‘‘the presence
of which in the ambient air results from
numerous or diverse mobile or
stationary sources’’; and for which he
‘‘plans to issue air quality
criteria. . . .’’ (42 U.S.C. 7408(a)(1)).
Air quality criteria are intended to
‘‘accurately reflect the latest scientific
knowledge useful in indicating the kind
and extent of all identifiable effects on
public health or welfare which may be
expected from the presence of [a]
pollutant in the ambient air. . . .’’ (42
U.S.C. 7408(a)(2)).
Section 109 [42 U.S.C. 7409] directs
the Administrator to propose and
promulgate ‘‘primary’’ and ‘‘secondary’’
NAAQS for pollutants for which air
quality criteria are issued [42 U.S.C.
7409(a)]. Section 109(b)(1) defines
primary standards as ones ‘‘the
attainment and maintenance of which in
the judgment of the Administrator,
based on such criteria and allowing an
adequate margin of safety, are requisite
to protect the public health.’’ 5 Under
5 The legislative history of section 109 indicates
that a primary standard is to be set at ‘‘the
maximum permissible ambient air level . . . which
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section 109(b)(2), a secondary standard
must ‘‘specify a level of air quality the
attainment and maintenance of which,
in the judgment of the Administrator,
based on such criteria, is requisite to
protect the public welfare from any
known or anticipated adverse effects
associated with the presence of [the]
pollutant in the ambient air.’’ 6
In setting primary and secondary
standards that are ‘‘requisite’’ to protect
public health and welfare, respectively,
as provided in section 109(b), the EPA’s
task is to establish standards that are
neither more nor less stringent than
necessary. In so doing, the EPA may not
consider the costs of implementing the
standards. See generally Whitman v.
American Trucking Associations, 531
U.S. 457, 465–472, 475–76 (2001).
Likewise, ‘‘[a]ttainability and
technological feasibility are not relevant
considerations in the promulgation of
national ambient air quality standards.’’
American Petroleum Institute v. Costle,
665 F.2d 1176, 1185 (D.C. Cir. 1981);
accord Murray Energy Corporation v.
EPA, 936 F.3d 597, 623–24 (D.C. Cir.
2019).
The requirement that primary
standards provide an adequate margin
of safety was intended to address
uncertainties associated with
inconclusive scientific and technical
information available at the time of
standard setting. It was also intended to
provide a reasonable degree of
protection against hazards that research
has not yet identified. See Lead
Industries Association v. EPA, 647 F.2d
1130, 1154 (D.C. Cir 1980); American
Petroleum Institute v. Costle, 665 F.2d at
1186; Coalition of Battery Recyclers
Ass’n v. EPA, 604 F.3d 613, 617–18
(D.C. Cir. 2010); Mississippi v. EPA, 744
F.3d 1334, 1353 (D.C. Cir. 2013). Both
kinds of uncertainties are components
of the risk associated with pollution at
levels below those at which human
health effects can be said to occur with
reasonable scientific certainty. Thus, in
selecting primary standards that include
an adequate margin of safety, the
Administrator is seeking not only to
prevent pollution levels that have been
demonstrated to be harmful but also to
will protect the health of any [sensitive] group of
the population,’’ and that for this purpose
‘‘reference should be made to a representative
sample of persons comprising the sensitive group
rather than to a single person in such a group.’’ S.
Rep. No. 91–1196, 91st Cong., 2d Sess. 10 (1970).
6 Under CAA section 302(h) (42 U.S.C. 7602(h)),
effects on welfare include, but are not limited to,
‘‘effects on soils, water, crops, vegetation, manmade
materials, animals, wildlife, weather, visibility, and
climate, damage to and deterioration of property,
and hazards to transportation, as well as effects on
economic values and on personal comfort and wellbeing.’’
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prevent lower pollutant levels that may
pose an unacceptable risk of harm, even
if the risk is not precisely identified as
to nature or degree. The CAA does not
require the Administrator to establish a
primary NAAQS at a zero-risk level or
at background concentration levels, see
Lead Industries Ass’n v. EPA, 647 F.2d
at 1156 n.51, Mississippi v. EPA, 744
F.3d at 1351, but rather at a level that
reduces risk sufficiently so as to protect
public health with an adequate margin
of safety.
In addressing the requirement for an
adequate margin of safety, the EPA
considers such factors as the nature and
severity of the health effects involved,
the size of the sensitive population(s),
and the kind and degree of
uncertainties. The selection of any
particular approach to providing an
adequate margin of safety is a policy
choice left specifically to the
Administrator’s judgment. See Lead
Industries Ass’n v. EPA, 647 F.2d at
1161–62; Mississippi v. EPA, 744 F.3d at
1353.
Section 109(d)(1) of the Act requires
the review every five years of existing
air quality criteria and, if appropriate,
the revision of those criteria to reflect
advances in scientific knowledge on the
effects of the pollutant on public health
and welfare. Under the same provision,
the EPA is also to review every five
years and, if appropriate, revise the
NAAQS, based on the revised air quality
criteria.
Section 109(d)(2) addresses the
appointment and advisory functions of
an independent scientific review
committee. Section 109(d)(2)(A)
requires the Administrator to appoint
this committee, which is to be
composed of ‘‘seven members including
at least one member of the National
Academy of Sciences, one physician,
and one person representing State air
pollution control agencies.’’ Section
109(d)(2)(B) provides that the
independent scientific review
committee ‘‘shall complete a review of
the criteria . . . and the national
primary and secondary ambient air
quality standards . . . and shall
recommend to the Administrator any
new . . . standards and revisions of
existing criteria and standards as may be
appropriate. . . .’’ Since the early
1980s, this independent review function
has been performed by the Clean Air
Scientific Advisory Committee (CASAC)
of the EPA’s Science Advisory Board.
As previously noted, the Supreme
Court has held that section 109(b)
‘‘unambiguously bars cost
considerations from the NAAQS-setting
process.’’ Whitman v. Am. Trucking
Associations, 531 U.S. 457, 471 (2001).
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Accordingly, while some of these issues
regarding which Congress has directed
the CASAC to advise the Administrator
are ones that are relevant to the standard
setting process, others are not. Issues
that are not relevant to standard setting
may be relevant to implementation of
the NAAQS once they are established.7
B. Related PM Control Programs
States are primarily responsible for
ensuring attainment and maintenance of
ambient air quality standards once the
EPA has established them. Under
section 110 and Part D, Subparts 1, 4
and 6 of the CAA, and related
provisions and regulations, states are to
submit, for the EPA’s approval, state
implementation plans (SIPs) that
provide for the attainment and
maintenance of such standards through
control programs directed to sources of
the pollutants involved. The states, in
conjunction with the EPA, also
administer the prevention of significant
deterioration of air quality program that
covers these pollutants (see 42 U.S.C.
7470–7479). In addition, Federal
programs provide for or result in
nationwide reductions in emissions of
PM and its precursors under Title II of
the Act, 42 U.S.C. 7521–7574, which
involves controls for motor vehicles and
nonroad engines and equipment; the
new source performance standards
under section 111 of the Act, 42 U.S.C.
7411; and the national emissions
standards for hazardous pollutants
under section 112 of the Act, 42 U.S.C.
7412.
C. Review of the Air Quality Criteria and
Standards for Particulate Matter
1. Reviews Completed in 1971 and 1987
The EPA first established NAAQS for
PM in 1971 (36 FR 8186, April 30,
1971), based on the original Air Quality
7 Some aspects of the CASAC’s advice may not be
relevant to the EPA’s process of setting primary and
secondary standards that are requisite to protect
public health and welfare. Indeed, were the EPA to
consider costs of implementation when reviewing
and revising the standards ‘‘it would be grounds for
vacating the NAAQS.’’ Whitman, 531 U.S. at 471
n.4. At the same time, the CAA directs the CASAC
to provide advice on ‘‘any adverse public health,
welfare, social, economic, or energy effects which
may result from various strategies for attainment
and maintenance’’ of the NAAQS to the
Administrator under section 109(d)(2)(C)(iv). In
Whitman, the Court clarified that most of that
advice would be relevant to implementation but not
standard setting, as it ‘‘enable[s] the Administrator
to assist the States in carrying out their statutory
role as primary implementers of the NAAQS.’’ Id.
at 470 (emphasis in original). However, the Court
also noted that the CASAC’s ‘‘advice concerning
certain aspects of ‘adverse public health . . .
effects’ from various attainment strategies is
unquestionably pertinent’’ to the NAAQS
rulemaking record and relevant to the standard
setting process. Id. at 470 n.2.
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Criteria Document (AQCD) (DHEW,
1969).8 The Federal reference method
(FRM) specified for determining
attainment of the original standards was
the high-volume sampler, which
collects PM up to a nominal size of 25
to 45 mm (referred to as total suspended
particulates or TSP). The primary
standards were set at 260 mg/m3, 24hour average, not to be exceeded more
than once per year, and 75 mg/m3,
annual geometric mean. The secondary
standards were set at 150 mg/m3, 24hour average, not to be exceeded more
than once per year, and 60 mg/m3,
annual geometric mean.
In October 1979 (44 FR 56730,
October 2, 1979), the EPA announced
the first periodic review of the air
quality criteria and NAAQS for PM.
Revised primary and secondary
standards were promulgated in 1987 (52
FR 24634, July 1, 1987). In the 1987
decision, the EPA changed the indicator
for particles from TSP to PM10, in order
to focus on the subset of inhalable
particles small enough to penetrate to
the thoracic region of the respiratory
tract (including the tracheobronchial
and alveolar regions), referred to as
thoracic particles.9 The level of the 24hour standards (primary and secondary)
was set at 150 mg/m3, and the form was
one expected exceedance per year, on
average over three years. The level of
the annual standards (primary and
secondary) was set at 50 mg/m3, and the
form was annual arithmetic mean,
averaged over three years.
2. Review Completed in 1997
In April 1994, the EPA announced its
plans for the second periodic review of
the air quality criteria and NAAQS for
PM, and in 1997 the EPA promulgated
revisions to the NAAQS (62 FR 38652,
July 18, 1997). In the 1997 decision, the
EPA determined that the fine and coarse
fractions of PM10 should be considered
separately. This determination was
based on evidence that serious health
effects were associated with short- and
long-term exposures to fine particles in
areas that met the existing PM10
standards. The EPA added new
standards, using PM2.5 as the indicator
for fine particles (with PM2.5 referring to
particles with a nominal mean
aerodynamic diameter less than or equal
to 2.5 mm). The new primary standards
8 Prior to the review initiated in 2007 (see below),
the AQCD provided the scientific foundation (i.e.,
the air quality criteria) for the NAAQS. Beginning
in that review, the Integrated Science Assessment
(ISA) has replaced the AQCD.
9 PM
10 refers to particles with a nominal mean
aerodynamic diameter less than or equal to 10 mm.
More specifically, 10 mm is the aerodynamic
diameter for which the efficiency of particle
collection is 50 percent.
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were as follows: (1) an annual standard
with a level of 15.0 mg/m3, based on the
3-year average of annual arithmetic
mean PM2.5 concentrations from single
or multiple community-oriented
monitors;10 and (2) a 24-hour standard
with a level of 65 mg/m3, based on the
3-year average of the 98th percentile of
24-hour PM2.5 concentrations at each
monitor within an area. Also, the EPA
established a new reference method for
the measurement of PM2.5 in the
ambient air and adopted rules for
determining attainment of the new
standards. To continue to address the
health effects of the coarse fraction of
PM10 (referred to as thoracic coarse
particles or PM10–2.5; generally including
particles with a nominal mean
aerodynamic diameter greater than 2.5
mm and less than or equal to 10 mm), the
EPA retained the primary annual PM10
standard and revised the form of the
primary 24-hour PM10 standard to be
based on the 99th percentile of 24-hour
PM10 concentrations at each monitor in
an area. The EPA revised the secondary
standards by setting them equal in all
respects to the primary standards.
Following promulgation of the 1997
PM NAAQS, petitions for review were
filed by several parties, addressing a
broad range of issues. In May 1999, the
U.S. Court of Appeals for the District of
Columbia Circuit (D.C. Circuit) upheld
the EPA’s decision to establish fine
particle standards, holding that ‘‘the
growing empirical evidence
demonstrating a relationship between
fine particle pollution and adverse
health effects amply justifies
establishment of new fine particle
standards.’’ American Trucking
Associations, Inc. v. EPA, 175 F. 3d
1027, 1055–56 (D.C. Cir. 1999). The D.C.
Circuit also found ‘‘ample support’’ for
the EPA’s decision to regulate coarse
particle pollution, but vacated the 1997
PM10 standards, concluding that the
EPA had not provided a reasonable
explanation justifying use of PM10 as an
indicator for coarse particles. American
Trucking Associations v. EPA, 175 F. 3d
at 1054–55. Pursuant to the D.C.
Circuit’s decision, the EPA removed the
vacated 1997 PM10 standards, and the
10 The 1997 annual PM
2.5 standard was compared
with measurements made at the communityoriented monitoring site recording the highest
concentration or, if specific constraints were met,
measurements from multiple community-oriented
monitoring sites could be averaged (i.e., ‘‘spatial
averaging’’). In the last review (completed in 2012)
the EPA replaced the term ‘‘community-oriented’’
monitor with the term ‘‘area-wide’’ monitor. Areawide monitors are those sited at the neighborhood
scale or larger, as well as those monitors sited at
micro- or middle-scales that are representative of
many such locations in the same core-based
statistical area (CBSA) (78 FR 3236, January 15,
2013).
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5565
pre-existing 1987 PM10 standards
remained in place (65 FR 80776,
December 22, 2000). The D.C. Circuit
also upheld the EPA’s determination not
to establish more stringent secondary
standards for fine particles to address
effects on visibility. American Trucking
Associations v. EPA, 175 F. 3d at 1027.
The D.C. Circuit also addressed more
general issues related to the NAAQS,
including issues related to the
consideration of costs in setting NAAQS
and the EPA’s approach to establishing
the levels of NAAQS. Regarding the cost
issue, the court reaffirmed prior rulings
holding that in setting NAAQS the EPA
is ‘‘not permitted to consider the cost of
implementing those standards.’’
American Trucking Associations v.
EPA, 175 F. 3d at 1040–41. Regarding
the levels of NAAQS, the court held that
the EPA’s approach to establishing the
level of the standards in 1997 (i.e., both
for PM and for the ozone NAAQS
promulgated on the same day) effected
‘‘an unconstitutional delegation of
legislative authority.’’ American
Trucking Associations v. EPA, 175 F. 3d
at 1034–40. Although the court stated
that ‘‘the factors EPA uses in
determining the degree of public health
concern associated with different levels
of ozone and PM are reasonable,’’ it
remanded the rule to the EPA, stating
that when the EPA considers these
factors for potential non-threshold
pollutants ‘‘what EPA lacks is any
determinate criterion for drawing lines’’
to determine where the standards
should be set.
The D.C. Circuit’s holding on the cost
and constitutional issues were appealed
to the United States Supreme Court. In
February 2001, the Supreme Court
issued a unanimous decision upholding
the EPA’s position on both the cost and
constitutional issues. Whitman v.
American Trucking Associations, 531
U.S. 457, 464, 475–76. On the
constitutional issue, the Court held that
the statutory requirement that NAAQS
be ‘‘requisite’’ to protect public health
with an adequate margin of safety
sufficiently guided the EPA’s discretion,
affirming the EPA’s approach of setting
standards that are neither more nor less
stringent than necessary.
The Supreme Court remanded the
case to the D.C. Circuit for resolution of
any remaining issues that had not been
addressed in that court’s earlier rulings.
Id. at 475–76. In a March 2002 decision,
the D.C. Circuit rejected all remaining
challenges to the standards, holding that
the EPA’s PM2.5 standards were
reasonably supported by the
administrative record and were not
‘‘arbitrary and capricious.’’ American
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3. Review Completed in 2006
In October 1997, the EPA published
its plans for the third periodic review of
the air quality criteria and NAAQS for
PM (62 FR 55201, October 23, 1997).
After the CASAC and public review of
several drafts, the EPA’s National Center
for Environmental Assessment (NCEA)
finalized the AQCD in October 2004
(U.S. EPA, 2004a). The EPA’s Office of
Air Quality Planning and Standards
(OAQPS) finalized a Risk Assessment
and Staff Paper in December 2005 (Abt
Associates, 2005; U.S. EPA, 2005).11 On
December 20, 2005, the EPA announced
its proposed decision to revise the
NAAQS for PM and solicited public
comment on a broad range of options
(71 FR 2620, January 17, 2006). On
September 21, 2006, the EPA
announced its final decisions to revise
the primary and secondary NAAQS for
PM to provide increased protection of
public health and welfare, respectively
(71 FR 61144, October 17, 2006). With
regard to the primary and secondary
standards for fine particles, the EPA
revised the level of the 24-hour PM2.5
standards to 35 mg/m3, retained the level
of the annual PM2.5 standards at 15.0 mg/
m3, and revised the form of the annual
PM2.5 standards by narrowing the
constraints on the optional use of spatial
averaging. With regard to the primary
and secondary standards for PM10, the
EPA retained the 24-hour standards,
with levels at 150 mg/m3, and revoked
the annual standards.12 The
Administrator judged that the available
evidence generally did not suggest a
link between long-term exposure to
existing ambient levels of coarse
particles and health or welfare effects.
In addition, a new reference method
was added for the measurement of
11 Prior to the review initiated in 2007, the Staff
Paper presented the EPA staff’s considerations and
conclusions regarding the adequacy of existing
NAAQS and, when appropriate, the potential
alternative standards that could be supported by the
evidence and information. More recent reviews
present this information in the Policy Assessment.
12 In the 2006 proposal, the EPA proposed to
revise the 24-hour PM10 standard in part by
establishing a new PM10–2.5 indicator for thoracic
coarse particles (i.e., particles generally between 2.5
and 10 mm in diameter). The EPA proposed to
include any ambient mix of PM10–2.5 that was
dominated by resuspended dust from high density
traffic on paved roads and by PM from industrial
sources and construction sources. The EPA
proposed to exclude any ambient mix of PM10–2.5
that was dominated by rural windblown dust and
soils and by PM generated from agricultural and
mining sources. In the final decision, the existing
PM10 standard was retained, in part due to an
‘‘inability . . . to effectively and precisely identify
which ambient mixes are included in the [PM10–2.5]
indicator and which are not’’ (71 FR 61197, October
17, 2006).
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PM10–2.5 in the ambient air in order to
provide a basis for approving Federal
equivalent methods (FEMs) and to
promote the gathering of scientific data
to support future reviews of the PM
NAAQS.
Several parties filed petitions for
review following promulgation of the
revised PM NAAQS in 2006. These
petitions addressed the following issues:
(1) Selecting the level of the primary
annual PM2.5 standard; (2) retaining
PM10 as the indicator of a standard for
thoracic coarse particles, retaining the
level and form of the 24-hour PM10
standard, and revoking the PM10 annual
standard; and (3) setting the secondary
PM2.5 standards identical to the primary
standards. On February 24, 2009, the
D.C. Circuit issued its opinion in the
case American Farm Bureau Federation
v. EPA, 559 F. 3d 512 (D.C. Cir. 2009).
The court remanded the primary annual
PM2.5 NAAQS to the EPA because the
Agency had failed to adequately explain
why the standards provided the
requisite protection from both shortand long-term exposures to fine
particles, including protection for at-risk
populations. Id. at 520–27. With regard
to the standards for PM10, the court
upheld the EPA’s decisions to retain the
24-hour PM10 standard to provide
protection from thoracic coarse particle
exposures and to revoke the annual
PM10 standard. Id. at 533–38. With
regard to the secondary PM2.5 standards,
the court remanded the standards to the
EPA because the Agency failed to
adequately explain why setting the
secondary PM standards identical to the
primary standards provided the
required protection for public welfare,
including protection from visibility
impairment. Id. at 528–32. The EPA
responded to the court’s remands as part
of the next review of the PM NAAQS,
which was initiated in 2007 (discussed
below).
4. Review Completed in 2012
In June 2007, the EPA initiated the
fourth periodic review of the air quality
criteria and the PM NAAQS by issuing
a call for information (72 FR 35462, June
28, 2007). Based on the NAAQS review
process, as revised in 2008 and again in
2009,13 the EPA held science/policy
issue workshops on the primary and
secondary PM NAAQS (72 FR 34003,
June 20, 2007; 72 FR 34005, June 20,
2007), and prepared and released the
planning and assessment documents
that comprise the review process (i.e.,
13 The
history of the NAAQS review process,
including revisions to the process, is discussed
athttps://www.epa.gov/naaqs/historicalinformation-naaqs-review-process.
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integrated review plan (IRP) (U.S. EPA,
2008), ISA (U.S. EPA, 2009a), REA
planning documents for health and
welfare (U.S. EPA, 2009a, U.S. EPA,
2009c), a quantitative health risk
assessment (U.S. EPA, 2009a, U.S. EPA,
2009c), a quantitative health risk
assessment (U.S. EPA, 2010b) and an
urban-focused visibility assessment
(U.S. EPA, 2010a), and PA (U.S. EPA,
2011). In June 2012, the EPA announced
its proposed decision to revise the
NAAQS for PM (77 FR 38890, June 29,
2012).
In December 2012, the EPA
announced its final decisions to revise
the primary NAAQS for PM to provide
increased protection of public health (78
FR 3086, January 15, 2013). With regard
to primary standards for PM2.5, the EPA
revised the level of the annual PM2.5
standard 14 to 12.0 mg/m3 and retained
the 24-hour PM2.5 standard, with its
level of 35 mg/m3. For the primary PM10
standard, the EPA retained the 24-hour
standard to continue to provide
protection against effects associated
with short-term exposure to thoracic
coarse particles (i.e., PM10–2.5). With
regard to the secondary PM standards,
the EPA generally retained the 24-hour
and annual PM2.5 standards 15 and the
24-hour PM10 standard to address
visibility and non-visibility welfare
effects.
As with previous reviews, petitioners
challenged the EPA’s final rule.
Petitioners argued that the EPA acted
unreasonably in revising the level and
form of the annual standard and in
amending the monitoring network
provisions. On judicial review, the
revised standards and monitoring
requirements were upheld in all
respects. NAM v EPA, 750 F.3d 921
(D.C. Cir. 2014).
5. Review Completed in 2020
In December 2014, the EPA
announced the initiation of the current
periodic review of the air quality criteria
for PM and of the PM2.5 and PM10
NAAQS and issued a call for
information (79 FR 71764, December 3,
2014). On February 9 to 11, 2015, the
EPA’s NCEA and OAQPS held a public
workshop to inform the planning for the
review of the PM NAAQS (announced
in 79 FR 71764, December 3, 2014).
Workshop participants, including a
wide range of external experts as well as
the EPA staff representing a variety of
areas of expertise (e.g., epidemiology,
human and animal toxicology, risk/
14 The EPA also eliminated the option for spatial
averaging.
15 Consistent with the primary standard, the EPA
eliminated the option for spatial averaging with the
annual standard.
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exposure analysis, atmospheric science,
visibility impairment, climate effects),
were asked to highlight significant new
and emerging PM research, and to make
recommendations to the Agency
regarding the design and scope of the
review. This workshop provided for a
public discussion of the key science and
policy-relevant issues around which the
EPA structured the review of the PM
NAAQS and of the most meaningful
new scientific information that would
be available in the review to inform
understanding of these issues.
The input received at the workshop
guided the EPA staff in developing a
draft IRP, which was reviewed by the
CASAC Particulate Matter Panel and
discussed on public teleconferences
held in May 2016 (81 FR 13362, March
14, 2016) and August 2016 (81 FR
39043, June 15, 2016). Advice from the
CASAC, supplemented by the
Particulate Matter Panel, and input from
the public were considered in
developing the final IRP (U.S. EPA,
2016). The final IRP discusses the
approaches to be taken in developing
key scientific, technical, and policy
documents in the review and the key
policy-relevant issues that frame the
EPA’s consideration of whether the
primary and/or secondary NAAQS for
PM should be retained or revised.
In May 2018, the Administrator
issued a memorandum describing a
‘‘back-to-basics’’ process for reviewing
the NAAQS (Pruitt, 2018). This memo
announced the Agency’s intention to
conduct the review of the PM NAAQS
in such a manner as to ensure that any
necessary revisions were finalized by
December 2020. Following this memo,
on October 10, 2018, the Administrator
additionally announced that the role of
reviewing the key assessments
developed as part of the ongoing review
of the PM NAAQS (i.e., drafts of the ISA
and PA) would be performed by the
seven-member chartered CASAC (i.e.,
rather than the CASAC Particulate
Matter Panel that reviewed the draft
IRP).16
The EPA released the draft ISA in
October 2018 (83 FR 53471, October 23,
2018). The draft ISA was reviewed by
the chartered CASAC at a public
meeting held in Arlington, VA, in
December 2018 (83 FR 55529, November
6, 2018) and was discussed on a public
teleconference in March 2019 (84 FR
8523, March 8, 2019). The CASAC
provided its advice on the draft ISA in
a letter to the EPA Administrator dated
April 11, 2019 (Cox, 2019a). The EPA
16 Announcement available at: https://
www.regulations.gov/document/EPA-HQ-OAR2015-0072-0223.
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took steps to address these comments in
the final ISA, which was released in
December 2019 (U.S. EPA, 2019a).
The EPA released the draft PA in
September 2019 (84 FR 47944,
September 11, 2019). The draft PA was
reviewed by the chartered CASAC and
discussed in October 2019 at a public
meeting held in Cary, NC. Public
comments were received via a separate
public teleconference (84 FR 51555,
September 30, 2019). A public meeting
to discuss the chartered CASAC letter
and response to charge questions on the
draft PA was held in Cary, NC, in
December 2019 (84 FR 58713, November
1, 2019), and the CASAC provided its
advice on the draft PA, including its
advice on the current primary and
secondary PM standards, in a letter to
the EPA Administrator dated December
16, 2019 (Cox, 2019b). With regard to
the primary standards, the CASAC
recommended retaining the current 24hour PM2.5 and PM10 standards but did
not reach consensus on the adequacy of
the current annual PM2.5 standard. With
regard to the secondary standards, the
CASAC recommended retaining the
current standards. In response to the
CASAC’s comments, the 2020 final PA
incorporated a number of changes (U.S.
EPA, 2020a), as described in detail in
section I.C.5 of the 2020 proposal
document (85 FR 24100, April 30,
2020).
On April 14, 2020, the EPA proposed
to retain all of the primary and
secondary PM standards, without
revision. These proposed decisions were
published in the Federal Register on
April 30, 2020 (85 FR 24094, April 30,
2020). The EPA’s final decision on the
PM NAAQS was published in the
Federal Register on December 18, 2020
(85 FR 82684, December 18, 2020). In
the 2020 rulemaking, the EPA retained
the primary and secondary PM2.5 and
PM10 standards, without revision.
Following publication of the 2020
final action, several parties filed
petitions for review and petitions for
reconsideration of the EPA’s final
decision. The petitions for review were
filed in the D.C. Circuit and the Court
consolidated the cases. In order to
consider whether reconsideration of the
2020 final action was warranted, the
EPA moved for two 90-day abeyances in
these consolidated cases, which the
Court granted. After the EPA announced
that it is reconsidering the 2020 final
decision, the EPA filed a motion with
the Court to hold the consolidated cases
in abeyance until March 1, 2023, which
the court granted on October 1, 2021.
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6. Reconsideration of the 2020 PM
NAAQS Final Action
On January 20, 2021, President Biden
issued an ‘‘Executive Order on
Protecting Public Health and the
Environment and Restoring Science to
Tackle the Climate Crisis’’ (Executive
Order 13990; 86 FR 7037, January 25,
2021),17 which directed review of
certain agency actions. An
accompanying fact sheet provided a
non-exclusive list of agency actions that
agency heads should review in
accordance with that order, including
the 2020 Particulate Matter NAAQS
Decision.18
a. Decision To Initiate a Reconsideration
On June 10, 2021, the Agency
announced its decision to reconsider the
2020 PM NAAQS final action.19 The
EPA is reconsidering the December 2020
decision because the available scientific
evidence and technical information
indicate that the current standards may
not be adequate to protect public health
and welfare, as required by the Clean
Air Act. The EPA noted that the 2020
PA concluded that the scientific
evidence and information supported
revising the level of the primary annual
PM2.5 standard to below the current
level of 12.0 mg/m3 while retaining the
primary 24-hour PM2.5 standard (U.S.
EPA, 2020a). The EPA also noted that
the 2020 PA concluded that the
available scientific evidence and
information supported retaining the
primary PM10 standard and secondary
PM standards without revision (U.S.
EPA, 2020a).
b. Process for Reconsideration of the
2020 PM NAAQS Decision
In its announcement of the
reconsideration of the PM NAAQS, the
Agency explained that, in support of the
reconsideration, it would develop a
supplement to the 2019 ISA and a
revised PA. The EPA also explained that
the draft ISA Supplement and draft PA
would be reviewed at a public meeting
by the CASAC, and the public would
have opportunities to comment on these
documents during the CASAC review
process, as well as to provide input
during the rulemaking through the
17 See https://www.whitehouse.gov/briefing-room/
presidential-actions/2021/01/20/executive-orderprotecting-public-health-and-environment-andrestoring-science-to-tackle-climate-crisis/.
18 See https://www.whitehouse.gov/briefing-room/
statements-releases/2021/01/20/fact-sheet-list-ofagency-actions-for-review/.
19 The press release for this announcement is
available at: https://www.epa.gov/newsreleases/epareexamine-health-standards-harmful-soot-previousadministration-left-unchanged.
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public comment process and public
hearings on the proposed rulemaking.
On March 31, 2021, the Administrator
announced his decision to reestablish
the membership of the CASAC to
‘‘ensure the agency received the best
possible scientific insight to support our
work to protect human health and the
environment.’’ 20 Consistent with this
memorandum, a call for nominations of
candidates to the EPA’s chartered
CASAC was published in the Federal
Register (86 FR 17146, April 1, 2021).
On June 17, 2021, the Administrator
announced his selection of the seven
members to serve on the chartered
CASAC.21 22 Additionally, a call for
nominations of candidates to a PMspecific panel was published in the
Federal Register (86 FR 33703, June 25,
2021). The members of the PM CASAC
panel were announced on August 30,
2021.23
The draft ISA Supplement was
released in September 2021 (U.S. EPA,
2021a; 86 FR 54186, September 30,
2021). The CASAC PM panel met at a
virtual public meeting in November
2021 to review the draft ISA
Supplement (86 FR 52673, September
22, 2021). A virtual public meeting was
then held in February 2022, and during
this meeting the chartered CASAC
considered the CASAC PM panel’s draft
letter to the Administrator on the draft
ISA Supplement (87 FR 958, January 7,
2022). The chartered CASAC provided
its advice on the draft ISA Supplement
in a letter to the EPA Administrator
dated March 18, 2022 (Sheppard,
2022b). The EPA took steps to address
these comments in the final ISA
Supplement, which was released in May
2022 (U.S. EPA, 2022a; hereafter
referred to as the ISA Supplement
throughout this document).
The evidence presented within the
2019 ISA, along with the targeted
identification and evaluation of new
scientific information in the ISA
Supplement, provides the scientific
basis for the reconsideration of the 2020
PM NAAQS final decision. The ISA
20 The press release for this announcement is
available at: https://www.epa.gov/newsreleases/
administrator-regan-directs-epa-reset-criticalscience-focused-federal-advisory.
21 The press release for this announcement is
available at: https://www.epa.gov/newsreleases/epaannounces-selections-charter-members-clean-airscientific-advisory-committee.
22 The list of members of the chartered CASAC
and their biosketches are available at: https://
casac.epa.gov/ords/sab/f?p=113:29:
1706195567016:::RP,29:P29_COMMITTEEON:
CASAC.
23 The list of members of the PM CASAC panel
and their biosketches are available at: https://
casac.epa.gov/ords/sab/f?p=105:14:
9979229564047:::14:P14_COMMITTEEON:2021
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Supplement focuses on a thorough
evaluation of some studies that became
available after the literature cutoff date
of the 2019 ISA that could either further
inform the adequacy of the current PM
NAAQS or address key scientific topics
that have evolved since the literature
cutoff date for the 2019 ISA. In selecting
the health effects to evaluate within the
ISA Supplement, the EPA focused on
health effects for which the evidence
supported a ‘‘causal relationship’’
because those were the health effects
that were most useful in informing
conclusions in the 2020 PA (U.S. EPA,
2022a, section 1.2.1).24 Consistent with
the rationale for the focus on certain
health effects, in selecting the nonecological welfare effects to evaluate
within the ISA supplement, the EPA
focused on the non-ecological welfare
effects for which the evidence
supported a ‘‘causal relationship’’ and
for which quantitative analyses could be
supported by the evidence because
those were the welfare effects that were
most useful in informing conclusions in
the 2020 PA.25 Specifically, for non24 As described in section 1.2.1 of the ISA
Supplement: ‘‘In considering the public health
protection provided by the current primary PM2.5
standards, and the protection that could be
provided by alternatives, [the U.S. EPA, within the
2020 PM PA] emphasized health outcomes for
which the ISA determined that the evidence
supports either a ‘causal’ or a ‘likely to be causal’
relationship with PM2.5 exposures’’ (U.S. EPA,
2020a). Although the 2020 PA initially focused on
this broader set of evidence, the basis of the
discussion on potential alternative standards
primarily focused on health effect categories where
the 2019 PM ISA concluded a ‘causal relationship’
(i.e., short- and long-term PM2.5 exposure and
cardiovascular effects and mortality) as reflected in
Figures 3–7 and 3–8 of the 2020 PA (U.S. EPA,
2020a).’’ As described in section 1.2.1 of the ISA
Supplement: ‘‘In considering the public health
protection provided by the current primary PM2.5
standards, and the protection that could be
provided by alternatives, [the U.S. EPA, within the
2020 PM PA] emphasized health outcomes for
which the ISA determined that the evidence
supports either a ‘causal’ or a ‘likely to be causal’
relationship with PM2.5 exposures’’ (U.S. EPA,
2020a). Although the 2020 PA initially focused on
this broader set of evidence, the basis of the
discussion on potential alternative standards
primarily focused on health effect categories where
the 2019 PM ISA concluded a ‘causal relationship’
(i.e., short- and long-term PM2.5 exposure and
cardiovascular effects and mortality) as reflected in
Figures 3–7 and 3–8 of the 2020 PA (U.S. EPA,
2020a).’’
25 As described in section 1.2.1 of the ISA
Supplement: ‘‘The 2019 PM ISA concluded a
‘causal relationship’ for each of the welfare effects
categories evaluated (i.e., visibility, climate effects
and materials effects). While the 2020 PA
considered the broader set of evidence for these
effects, for climate effects and material effects, it
concluded that there remained ‘substantial
uncertainties with regard to the quantitative
relationships with PM concentrations and
concentration patterns that limit[ed] [the] ability to
quantitatively assess the public welfare protection
provided by the standards from these effects’ (U.S.
EPA, 2020a).’’
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ecological welfare effects, the focus
within the ISA Supplement is on
visibility effects. The ISA Supplement
also considers recent health effects
evidence that addresses key scientific
topics where the literature has evolved
since the 2020 review was completed,
specifically since the literature cutoff
date for the 2019 ISA.26
Building on the rationale presented in
section 1.2.1, the ISA Supplement
considers peer-reviewed studies
published from approximately January
2018 through March 2021 that meet the
following criteria:
Health Effects
Æ U.S. and Canadian epidemiologic
studies for health effect categories
where the 2019 ISA concluded a
‘‘causal relationship’’ (i.e., short- and
long-term PM2.5 exposure and
cardiovascular effects and mortality).
D U.S. and Canadian epidemiologic
studies that employed alternative
methods for confounder control or
conducted accountability analyses (i.e.,
examined the effect of a policy on
reducing PM2.5 concentrations).
• Welfare Effects
Æ U.S. and Canadian studies that
provide new information on public
preferences for visibility impairment
and/or developed methodologies or
conducted quantitative analyses of light
extinction.
• Key Scientific Topics
Æ Experimental studies (i.e.,
controlled human exposure and animal
toxicological) conducted at nearambient PM2.5 concentrations
experienced in the U.S.
Æ U.S.- and Canadian-based
epidemiologic studies that examined the
relationship between PM2.5 exposures
and severe acute respiratory syndrome
coronavirus 2 (SARS–CoV–2) infection
and coronavirus disease 2019 (COVID–
19) death.
Æ At-Risk Populations:
D U.S.- and Canadian-based
epidemiologic or exposure studies
examining potential disparities in either
PM2.5 exposures or the risk of health
26 These key scientific topics include
experimental studies conducted at near-ambient
concentrations, epidemiologic studies that
employed alternative methods for confounder
control or conducted accountability analyses,
studies that assess the relationship between PM2.5
exposure and severe acute respiratory syndrome
coronavirus 2 (SARS–CoV–2) infection and
coronavirus disease 2019 (COVID–19) death; and in
accordance with recent EPA goals on addressing
environmental justice, studies that examine
disparities in PM2.5 exposure and the risk of health
effects by race/ethnicity or socioeconomic status
(SES) (U.S. EPA, 2022a, section 1.2.1).
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effects by race/ethnicity or
socioeconomic status (SES).
Given the narrow scope of the ISA
Supplement, it is important to recognize
that the evaluation does not encompass
the full multidisciplinary evaluation
presented within the 2019 ISA that
would result in weight-of-evidence
conclusions on causality (i.e., causality
determinations). The ISA Supplement
critically evaluates and provides key
study specific information for those
recent studies deemed to be of greatest
significance for informing preliminary
conclusions on the PM NAAQS in the
context of the body of evidence and
scientific conclusions presented in the
2019 ISA. In its review of the draft ISA
Supplement, the CASAC noted that they
found ‘‘the Draft ISA Supplement to be
a well-written, comprehensive
evaluation of the new scientific
information published since the 2019
PM ISA’’ (Sheppard, 2022b, p. 2 of
letter). Furthermore, the CASAC stated
that ‘‘the final Integrated Science
Assessment (ISA) Supplement . . .
deserve[s] the Administrator’s full
consideration and [is] adequate for
rulemaking’’ (Sheppard, 2022b, p. 2 of
letter). However, recognizing the limited
scope of the draft ISA Supplement, the
CASAC stated that ‘‘[a]lthough this
limitation is appropriate for the targeted
purpose of the Draft ISA Supplement
. . . this limiting of scope applies only
to this document and is not intended to
establish a precedent for future ISAs’’
(Sheppard, 2022b, p. 2 of letter).
The draft PA was released in October
2021 (86 FR 56263, October 8, 2021).
The CASAC PM panel met at a virtual
public meeting in December 2021 to
review the draft PA (86 FR 52673,
September 22, 2021). A virtual public
meeting was then held in February 2022
and March 2022, and during this
meeting the chartered CASAC
considered the CASAC PM panel’s draft
letter to the Administrator on the draft
PA (87 FR 958, January 7, 2022). The
chartered CASAC provided its advice on
the draft PA in a letter to the EPA
Administrator dated March 18, 2022
(Sheppard, 2022a). The EPA took steps
to address these comments in revising
and finalizing the PA. The PA considers
the scientific evidence presented in the
2019 ISA and ISA Supplement and
considers the quantitative and technical
information presented in the 2020 PA,
along with updated and newly available
analyses since the completion of the
2020 review. For those health and
welfare effects for which the ISA
Supplement evaluated recently
available evidence and for which
updated quantitative analyses were
supported (i.e., PM2.5-related health
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effects and visibility effects), the PA
includes consideration of this newly
available scientific and technical
information in reaching preliminary
conclusions. For those health and
welfare effects for which newly
available scientific and technical
information were not evaluated (i.e.,
PM10–2.5-related health effects and nonvisibility effects), the conclusions
presented in the PA rely heavily on the
information that supported the
conclusions in the 2020 PA. The final
PA was released in May 2022 (U.S. EPA,
2022b; hereafter referred to as the PA
throughout this document).
D. Air Quality Information
This section provides a summary of
basic information related to PM ambient
air quality. It summarizes information
on the distribution of particle size in
ambient air (section I.D.1), sources and
emissions contributing to PM in the
ambient air (section I.D.2), monitoring
ambient PM in the U.S. (section I.D.3),
ambient PM concentrations and trends
in the U.S. (I.D.4), characterizing
ambient PM2.5 concentrations for
exposure (section I.D.5), and
background PM (section I.D.6).
Additional detail on PM air quality can
be found in Chapter 2 of the PA (U.S.
EPA, 2022b).
1. Distribution of Particle Size in
Ambient Air
In ambient air, PM is a mixture of
substances suspended as small liquid
and/or solid particles (U.S. EPA, 2019a,
section 2.2) and distinct health and
welfare effects have been linked with
exposures to particles of different sizes.
Particles in the atmosphere range in size
from less than 0.01 to more than 10 mm
in diameter (U.S. EPA, 2019a, section
2.2). The EPA defines PM2.5, also
referred to as fine particles, as particles
with aerodynamic diameters generally
less than or equal to 2.5 mm. The size
range for PM10–2.5, also called coarse or
thoracic coarse particles, includes those
particles with aerodynamic diameters
generally greater than 2.5 mm and less
than or equal to 10 mm. PM10, which is
comprised of both fine and coarse
fractions, includes those particles with
aerodynamic diameters generally less
than or equal to 10 mm. In addition,
ultrafine particles (UFP) are often
defined as particles with a diameter of
less than 0.1 mm based on physical size,
thermal diffusivity or electrical mobility
(U.S. EPA, 2019a, section 2.2).
Atmospheric lifetimes are generally
longest for PM2.5, which often remains
in the atmosphere for days to weeks
(U.S. EPA, 2019a, Table 2–1) before
being removed by wet or dry deposition,
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while atmospheric lifetimes for UFP and
PM10–2.5 are shorter and are generally
removed from the atmosphere within
hours, through wet or dry deposition
(U.S. EPA, 2019a, Table 2–1; U.S. EPA,
2022b, section 2.1).
2. Sources and Emissions Contributing
to PM in the Ambient Air
PM is composed of both primary
(directly emitted particles) and
secondary particles. Primary PM is
derived from direct particle emissions
from specific PM sources while
secondary PM originates from gas-phase
precursor chemical compounds present
in the atmosphere that have participated
in new particle formation or condensed
onto existing particles (U.S. EPA, 2019a,
section 2.3). As discussed further in the
2019 ISA (U.S. EPA, 2019a, section
2.3.2.1), secondary PM is formed in the
atmosphere by photochemical oxidation
reactions of both inorganic and organic
gas-phase precursors. Precursor gases
include sulfur dioxide (SO2), nitrogen
oxides (NOX), and volatile organic
compounds (VOC) (U.S. EPA, 2019a,
section 2.3.2.1). Ammonia also plays an
important role in the formation of
nitrate PM by neutralizing sulfuric acid
and nitric acid. Sources and emissions
of PM are discussed in more detail the
PA (U.S. EPA, 2022b, section 2.1.1).
Briefly, anthropogenic sources of PM
include both stationary (e.g., fuel
combustion for electricity production
and other purposes, industrial
processes, agricultural activities) and
mobile (e.g., diesel- and gasolinepowered highway vehicles and other
engine-driven sources) sources. Natural
sources of PM include dust from the
wind erosion of natural surfaces, sea
salt, wildfires, primary biological
aerosol particles (PBAP) such as bacteria
and pollen, oxidation of biogenic
hydrocarbons, such as isoprene and
terpenes to produce secondary organic
aerosol (SOA), and geogenic sources,
such as sulfate formed from volcanic
production of SO2. Wildland fire, which
encompass both wildfire and prescribed
fire, accounts for over 30% of emissions
of primary PM2.5 emissions (U.S. EPA,
2021).
In recent years, the frequency and
magnitude of wildfires have increased
(U.S. EPA, 2019a). The magnitude of the
public health impact of wildfires is
substantial both because of the increase
in PM2.5 concentrations as well as the
duration of the wildfire smoke season,
which is considered to range from May
to November. Wildfire can make a large
contribution to air pollution (including
PM2.5), and wildfire events can threaten
public safety and life. The impacts of
wildfire events can be mitigated through
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management of wildland vegetation,
including through prescribed fire.
Prescribed fire (and some wildfires) can
mimic the natural processes necessary
to maintain fire dependent ecosystems,
minimizing catastrophic wildfires and
the risks they pose to safety, property
and air quality (see, e.g., 81 FR 58010,
58038, August 24, 2016). Landowners,
land managers and government public
safety agencies are strongly motivated to
reduce the frequency and severity of
human caused wildfires. Additionally,
land managers, landowners, air agencies
and communities may be able to lessen
the impacts of wildfires by working
collaboratively to take steps to minimize
fuel loading in areas vulnerable to fire.
Fuel load minimization steps can
consist of both prescribed fire and
mechanical treatments, such as using
mechanical equipment to reduce
accumulated understory (81 FR 68249,
October 3, 2016). There are specific
Federal plans of the Department of the
Interior 27 and United States Forest
Service 28 to increase fuel load
minimization efforts in areas at high risk
of wildfire. The recently passed
Bipartisan Infrastructure Law 29 and
Inflation Reduction Act 30 further direct
agencies and provide funding for such
efforts at the Federal level as well as at
state, Tribal, local, and private
landowner levels.31
Wildfire events produce high PM
emissions that impact the PM
concentrations in ambient air to the
extent that such days with high PM
concentrations from wildfire smoke
events may affect the design values in
a given area. The annual and daily
design values affected by potential
exceptional events associated with
wildfire smoke may qualify to be
excluded from design value calculations
used for comparison to the NAAQS. The
EPA’s Exceptional Events Rule (81 FR
68216, October 3, 2016) describes the
process by which exceedances caused
27 See U.S. Department of the Interior,
‘‘Infrastructure Investment and Jobs Act Wildfire
Risk Five-Year Monitoring, Maintenance, and
Treatment Plan’’ (April 2022), available at: https://
www.doi.gov/sites/doi.gov/files/bil-5-year-wildfirerisk-mmt-plan.04.2022.owf_.final_.pdf.
28 See U.S. Department of Agriculture, Forest
Service, ‘‘Confronting the Wildfire Crisis: A
Strategy for Protecting Communities and Improving
Resilience in America’s Forests’’, FS–1187d (April
2022) available at: https://www.fs.usda.gov/sites/
default/files/Confronting-Wildfire-Crisis.pdf.
29 Inflation Reduction Act, Public Law 117–169
available at https://www.congress.gov/117/plaws/
publ169/PLAW-117publ169.pdf.
30 Infrastructure Investment and Jobs Act, Public
Law 117–58, available at https://www.congress.gov/
117/plaws/publ58/PLAW-117publ58.pdf.
31 Inflation Reduction Act, Public Law 117–169
available at https://www.congress.gov/117/plaws/
publ169/PLAW-117publ169.pdf.
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by fire events, including certain
prescribed fires, can be excluded from
the design values. It should be noted
that potential exceptional events
associated with prescribed fires on
wildland may also qualify to be
excluded from design value calculations
used for comparison to the NAAQS
under the Exceptional Events Rule (as
described in more detail in section VIII
below).
While the EPA is not proposing
changes to implementation as a part of
this proposal (as described in more
detail in section VIII below), the EPA
acknowledges that increases in PM2.5
emissions due to increases in wildfire
and prescribed fire on wildland present
a number of challenges relevant to the
implementation of the PM NAAQS,
particularly if one or more standards are
strengthened. Stakeholders have
expressed concern about the growing
health challenges associated with such
emissions, the importance of prescribed
fire for managing fire-dependent
ecosystems and reducing fuel loads, and
the potential for further increases in the
frequency and magnitude of wildfires
due to climate change. Though such
issues are outside the scope of this
proposal, the EPA acknowledges that
these topics may arise in the context of
implementation of any revised PM2.5
NAAQS and intends to work with
stakeholders to address these issues.
3. Monitoring of Ambient PM
To promote uniform enforcement of
the air quality standards set forth under
the CAA and to achieve the degree of
public health and welfare protection
intended for the NAAQS, the EPA
established PM Federal Reference
Methods (FRMs) for both PM10 and
PM2.5 (appendices J and L to 40 CFR
part 50). Amended following the 2006
and 2012 PM NAAQS reviews, the
current PM monitoring network relies
on FRMs and automated continuous
Federal Equivalent Methods (FEMs), in
part to support changes necessary for
implementation of the revised PM
standards. The requirement for
measuring ambient air quality and
reporting ambient air quality data and
related information are the basis for
appendices A through E to 40 CFR part
58. More information on PM ambient
monitoring networks is available in
section 2.2 of the PA (U.S. EPA, 2022b).
The PM2.5 monitoring program is one
of the major ambient air monitoring
programs with a robust, nationally
consistent network of ambient air
monitoring sites providing mass and/or
chemical speciation measurements. For
most urban locations, PM2.5 monitors
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are sited at the neighborhood scale,32
where PM2.5 concentrations are
reasonably homogeneous throughout an
entire urban sub-region. In each CBSA
with a monitoring requirement, at least
one PM2.5 monitoring station
representing area-wide air quality is
sited in an area of expected maximum
concentration. By ensuring the area of
expected maximum concentration in a
CBSA has a site compared to both the
annual and 24-hour NAAQS, all other
similar locations are thus protected.
Sites that represent relatively unique
microscale, localized hot-spot, or
unique middle scale impact sites are
only eligible for comparison to the 24hour PM2.5 NAAQS.
There are three main methods
components of the PM2.5 monitoring
program: filter-based FRMs measuring
PM2.5 mass, FEMs measuring PM2.5
mass, and other samplers used to collect
the aerosol used in subsequent
laboratory analysis for measuring PM2.5
chemical speciation. The FRMs are
primarily used for comparison to the
NAAQS, but also serve other important
purposes, such as developing trends and
evaluating the performance of FEMs.
PM2.5 FEMs are typically continuous
methods used to support forecasting and
reporting of the Air Quality Index (AQI)
but are also used for comparison to the
NAAQS. Samplers that are part of the
Chemical Speciation Network (CSN)
and Interagency Monitoring of Protected
Visual Environments (IMPROVE)
network are used to provide chemical
composition of the aerosol and serve a
variety of objectives. More detail on of
each of these components of the PM2.5
monitoring program and of recent
changes to PM2.5 monitoring
requirements are described in detail in
the PA (U.S. EPA, 2022b, section 2.2.3).
4. Ambient Concentrations and Trends
This section summarizes available
information on recent ambient PM
concentrations in the U.S. and on trends
32 For PM , neighborhood scale is defined as
2.5
follows: Measurements in this category would
represent conditions throughout some reasonably
homogeneous urban sub-region with dimensions of
a few kilometers and of generally more regular
shape than the middle scale. Homogeneity refers to
the particulate matter concentrations, as well as the
land use and land surface characteristics. Much of
the PM2.5 exposures are expected to be associated
with this scale of measurement. In some cases, a
location carefully chosen to provide neighborhood
scale data would represent the immediate
neighborhood as well as neighborhoods of the same
type in other parts of the city. PM2.5 sites of this
kind provide good information about trends and
compliance with standards because they often
represent conditions in areas where people
commonly live and work for periods comparable to
those specified in the NAAQS. In general, most
PM2.5 monitoring in urban areas should have this
scale.
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in PM air quality. Sections I.D.4.a and
I.D.4.b summarize information on PM2.5
mass and components, respectively.
Section I.D.4.c summarizes information
on PM10. Sections I.D.4.d and I.D.4.e
summarize the more limited
information on PM10–2.5 and UFP,
respectively. Additional detail on PM
air quality and trends can be found in
the PA (U.S. EPA, 2022b, section 2.3).
a. PM2.5 Mass
At monitoring sites in the U.S.,
annual PM2.5 concentrations from 2017
to 2019 averaged 8.0 mg/m3 (with the
10th and 90th percentiles at 5.9 and
10.0 mg/m3, respectively) and the 98th
percentiles of 24-hour concentrations
averaged 21.3 mg/m3 (with the 10th and
90th percentiles at 14.0 and 29.7 mg/m3,
respectively) (U.S. EPA, 2022b, section
2.3.2.1). The highest ambient PM2.5
concentrations occur in the western
U.S., particularly in California and the
Pacific Northwest (U.S. EPA, 2022b,
Figure 2–15). Much of the eastern U.S.
has lower ambient concentrations, with
annual average concentrations generally
at or below 12.0 mg/m3 and 98th
percentiles of 24-hour concentrations
generally at or below 30 mg/m3 (U.S.
EPA, 2022b, section 2.3.2.1).
Recent ambient PM2.5 concentrations
reflect the substantial reductions that
have occurred across much of the U.S.
(U.S. EPA, 2022b, section 2.3.2.1). From
2000 to 2019, national annual average
PM2.5 concentrations declined from 13.5
mg/m3 to 7.6 mg/m3, a 43% decrease
(U.S. EPA, 2022b, section 2.3.2.1).33
These declines have occurred at urban
and rural monitoring sites, although
urban PM2.5 concentrations remain
consistently higher than those in rural
areas (Chan et al., 2018) due to the
impact of local sources in urban areas.
Analyses at individual monitoring sites
indicate that declines in ambient PM2.5
concentrations have been most
consistent across the eastern U.S. and in
parts of coastal California, where both
annual average and 98th percentiles of
24-hour concentrations declined
significantly (U.S. EPA, 2022b, section
2.3.2.1). In contrast, trends in ambient
PM2.5 concentrations have been less
consistent over much of the western
U.S., with no significant changes since
2000 observed at some sites in the
Pacific Northwest, the northern Rockies
and plains, and the southwest,
particularly for 98th percentiles of 24hour concentrations (U.S. EPA, 2022b,
section 2.3.2.1). As noted below, some
sites in the northwestern U.S. and
33 See https://www.epa.gov/air-trends/particulatematter-pm25-trends for up-to-date PM2.5 trends
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California, where wildfire have been
relatively common in recent years, have
experienced high concentrations over
shorter periods (i.e., 2-hour averages).
The recent deployment of PM2.5
monitors near major roads in large
urban areas provides information on
PM2.5 concentrations near an important
emissions source. For 2016–2018, Gantt
et al. (2021) reported that 52% and 24%
of the time near-road sites reported the
highest annual and 24-hour PM2.5
design value 34 in the CBSA,
respectively. Of the CBSAs with the
highest annual design values at nearroad sites reported by Gantt et al. (2021),
those design values were, on average,
0.8 mg/m3 higher than at the highest
measuring non-near-road sites (range is
0.1 to 2.1 mg/m3 higher at near-road
sites). Although most near-road
monitoring sites do not have sufficient
data to evaluate long-term trends in
near-road PM2.5 concentrations,
analyses of the data at one near-roadlike site in Elizabeth, NJ,35 show that the
annual average near-road increment has
generally decreased between 1999 and
2017 from about 2.0 mg/m3 to about 1.3
mg/m3 (U.S. EPA, 2022b, section
2.3.2.1).
Ambient PM2.5 concentrations can
exhibit a diurnal cycle that varies due
to impacts from intermittent emission
sources, meteorology, and atmospheric
chemistry. The PM2.5 monitoring
network in the U.S. has an increasing
number of continuous FEM monitors
reporting hourly PM2.5 mass
concentrations that reflect this diurnal
variation. The 2019 ISA describes a twopeaked diurnal pattern in urban areas,
with morning peaks attributed to rushhour traffic and afternoon peaks
attributed to a combination of rush hour
traffic, decreasing atmospheric dilution,
and nucleation (U.S. EPA, 2019a,
section 2.5.2.3, Figure 2–32). Because a
focus on annual average and 24-hour
average PM2.5 concentrations could
mask sub-daily patterns, and because
some health studies examine PM
exposure durations shorter than 24hours, it is useful to understand the
broader distribution of sub-daily PM2.5
concentrations across the U.S. The PA
presents information on the frequency
distribution of 2-hour average PM2.5
mass concentrations from all FEM PM2.5
monitors in the U.S. for 2017–2019. At
sites meeting the current primary PM2.5
34 A design value is considered valid if it meets
the data handling requirements given in appendix
N to 40 CFR part 50.
35 The Elizabeth Lab site in Elizabeth, NJ, is
situated approximately 30 meters from travel lanes
of the Interchange 13 toll plaza of the New Jersey
Turnpike and within 200 meters of travel lanes for
Interstate 278 and the New Jersey Turnpike.
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standards, these 2-hour concentrations
generally remain below 10 mg/m3, and
rarely exceed 30 mg/m3. Two-hour
concentrations are higher at sites
violating the current standards,
generally remaining below 16 mg/m3 and
rarely exceeding 80 mg/m3 (U.S. EPA,
2022b, section 2.3.2.2.3). The extreme
upper end of the distribution of 2-hour
PM2.5 concentrations is shifted higher
during the warmer months, generally
corresponding to the period of peak
wildfire frequency (April to September)
in the U.S. At sites meeting the current
primary standards, the highest 2-hour
concentrations measured rarely occur
outside of the period of peak wildfire
frequency. Most of the sites measuring
these very high concentrations are in the
northwestern U.S. and California, where
wildfires have been relatively common
in recent years (see U.S. EPA, 2022b,
Appendix A, Figure A–1). When the
period of peak wildfire frequency is
excluded from the analysis, the extreme
upper end of the distribution is reduced
(U.S. EPA, 2022b, section 2.3.2.2.3).
b. PM2.5 Components
Based on recent air quality data, the
major chemical components of PM2.5
have distinct spatial distributions.
Sulfate concentrations tend to be
highest in the eastern U.S., while in the
Ohio Valley, Salt Lake Valley, and
California nitrate concentrations are
highest, and relatively high
concentrations of organic carbon are
widespread across most of the
continental U.S. (U.S. EPA, 2022b,
section 2.3.2.3). Elemental carbon,
crustal material, and sea salt are found
to have the highest concentrations in the
northeast U.S., southwest U.S., and
coastal areas, respectively.
An examination of PM2.5 composition
trends can provide insight into the
factors contributing to overall
reductions in ambient PM2.5
concentrations. The biggest change in
PM2.5 composition that has occurred in
recent years is the reduction in sulfate
concentrations due to reductions in SO2
emissions. Between 2000 and 2015, the
nationwide annual average sulfate
concentration decreased by 17% at
urban sites and 20% at rural sites. This
change in sulfate concentrations is most
evident in the eastern U.S. and has
resulted in organic matter or nitrate now
being the greatest contributor to PM2.5
mass in many locations (U.S. EPA,
2019a, Figure 2–19). The overall
reduction in sulfate concentrations has
contributed substantially to the decrease
in national average PM2.5 concentrations
as well as the decline in the fraction of
PM10 mass accounted for by PM2.5 (U.S.
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EPA, 2019a, section 2.5.1.1.6; U.S. EPA,
2022b, section 2.3.1).
c. PM10
At long-term monitoring sites in the
U.S., the 2017–2019 average of 2nd
highest 24-hour PM10 concentration was
68 mg/m3 (with 10th and 90th
percentiles at 28 and 124 mg/m3,
respectively) (U.S. EPA, 2022b, section
2.3.2.4).36 The highest PM10
concentrations tend to occur in the
western U.S. Seasonal analyses indicate
that ambient PM10 concentrations are
generally higher in the summer months
than at other times of year, though the
most extreme high concentration events
are more likely in the spring (U.S. EPA,
2019a, Table 2–5). This is due to fact
that the major PM10 emission sources,
dust and agriculture, are more active
during the warmer and drier periods of
the year.
Recent ambient PM10 concentrations
reflect reductions that have occurred
across much of the U.S. (U.S. EPA,
2022b, section 2.3.2.4). From 2000 to
2019, 2nd highest 24-hour PM10
concentrations have declined by about
46% (U.S. EPA, 2022b, section
2.3.2.4).37 Analyses at individual
monitoring sites indicate that annual
average PM10 concentrations have
generally declined at most sites across
the U.S., with much of the decrease in
the eastern U.S. associated with
reductions in PM2.5 concentrations (U.S.
EPA, 2022b, section 2.3.2.4). Annual
2nd highest 24-hour PM10
concentrations have generally declined
in the eastern U.S., while concentrations
in much of the midwest and western
U.S. have remained unchanged or
increased since 2000 (U.S. EPA, 2022b,
section 2.3.2.4).
Compared to previous reviews, data
available from the NCore monitoring
network in the current reconsideration
allows a more comprehensive analysis
of the relative contributions of PM2.5
and PM10–2.5 to PM10 mass. PM2.5
generally contributes more to annual
average PM10 mass in the eastern U.S.
than the western U.S. (U.S. EPA, 2022b,
Figure 2–23). At most sites in the
eastern U.S., the majority of PM10 mass
is comprised of PM2.5. As ambient PM2.5
concentrations have declined in the
eastern U.S. (U.S. EPA, 2022b, section
2.3.2.2), the ratios of PM2.5 to PM10 have
also declined. For sites with days
having concurrently very high PM2.5 and
PM10 concentrations (U.S. EPA, 2022b,
36 The form of the current 24-hour PM
10 standard
is one-expected-exceedance, averaged over three
years.
37 For more information, see https://
www.epa.gov/air-trends/particulate-matter-pm10trends#pmnat.
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Figure 2–24), the PM2.5/PM10 ratios are
typically higher than the annual average
ratios. This is particularly true in the
northwestern U.S. where the high PM10
concentrations can occur during
wildfires with high PM2.5 (U.S. EPA,
2022b, section 2.3.2.4).
d. PM10–2.5
Since the 2012 review, the availability
of PM10–2.5 ambient concentration data
has greatly increased because of
additions to the PM10–2.5 monitoring
capabilities to the national monitoring
network. As illustrated in the PA (U.S.
EPA, 2022b, section 2.3.2.5), annual
average and 98th percentile PM10–2.5
concentrations exhibit less distinct
differences between the eastern and
western U.S. than for either PM2.5 or
PM10.
Due to the short atmospheric lifetime
of PM10–2.5 relative to PM2.5, many of the
high concentration sites are isolated and
likely near emission sources associated
with wind-blown and fugitive dust. The
spatial distributions of annual average
and 98th percentile concentrations of
PM10–2.5 are more similar than that of
PM2.5, suggesting that the same dustrelated emission sources are affecting
both long-term and episodic
concentrations (U.S. EPA, 2022b, Figure
2–25). The highest concentrations of
PM10–2.5 are in the southwest U.S. where
widespread dry and windy conditions
contribute to wind-blown dust
emissions. Additionally, compared to
PM2.5 and PM10, changes in PM10–2.5
concentrations have been small in
magnitude and inconsistent in direction
(U.S. EPA, 2022b, Figure 2–25). The
majority of PM10–2.5 sites in the U.S. do
not have a concentration trend from
2000–2019, reflecting the relatively
consistent level of dust emissions across
the U.S. during the same time period
(U.S. EPA, 2022b, section 2.3.2.5).38
e. UFP
Compared to PM2.5 mass, there is
relatively little data on U.S. particle
number concentrations, which are
dominated by UFP. In the published
literature, annual average particle
number concentrations reaching about
20,000 to 30,000 cm3 have been
reported in U.S. cities (U.S. EPA,
38 PM from dust emissions in the National
Emissions Inventory (NEI) remain fairly consistent
from year-to-year, except when there are severe
weather incursions or there is a dust event that
transports or causes major local dust storms to
occur (particularly in the western U.S.). These dust
events and weather incursions needed to effect dust
emissions on a national level are not common and
only seldomly occur. In the emissions trends
analysis presented in the PA (U.S. EPA, 2022b,
section 2.1.1), dust is included in the NEI sector
labeled ‘‘miscellaneous.’’
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2019a). In addition, based on UFP
measurements in two urban areas (New
York City, Buffalo) and at a background
site (Steuben County) in New York,
there is a pronounced difference in
particle number concentration between
different types of locations (U.S. EPA,
2022b, Figure 2–26; U.S. EPA, 2019a,
Figure 2–18). Urban particle number
counts were several times higher than at
the background site, and the highest
particle number counts in an urban area
with multiple sites (Buffalo) were
observed at a near-road location (U.S.
EPA, 2022b, section 2.3.2.6).
Long-term trends in UFP are not
routinely available at U.S. monitoring
sites. At one background site in Illinois
with long-term data available, the
annual average particle number
concentration declined between 2000
and 2019, closely matching the
reductions in annual PM2.5 mass over
that same period (U.S. EPA, 2022b,
section 2.3.2.6). In addition, a small
number of published studies have
examined UFP trends over time. While
limited, these studies also suggest that
UFP number concentrations have
declined over time along with decreases
in PM2.5 (U.S. EPA, 2022b, section
2.3.2.6). However, the relationship
between changes in ambient PM2.5 and
UFPs cannot be comprehensively
characterized due to the high variability
and limited monitoring of UFPs (U.S.
EPA, 2022b, section 2.3.2.6).
5. Characterizing Ambient PM2.5
Concentrations for Exposure
Epidemiologic studies use various
methods to characterize exposure to
ambient PM2.5. The methods used to
estimate PM2.5 concentrations can vary
from traditional methods using
monitoring data from ground-based
monitors to newer methods using more
complex hybrid modeling approaches.
Studies using hybrid modeling
approaches aim to broaden the spatial
coverage, as well as estimate more
spatially-resolved ambient PM2.5
concentrations, by expanding beyond
just those areas with monitors and
providing estimates in areas that do not
have ground-based monitors (i.e., areas
that are generally less densely
populated and tend to have lower PM2.5
concentrations) and at finer spatial
resolutions (e.g., 1 km x 1 km grid cells).
As such, the hybrid modeling
approaches tend to broaden the areas
captured in the exposure assessment,
and in doing so, the studies that utilize
these methods tend to report lower
mean PM2.5 concentrations than
monitor-based approaches. Further,
other aspects of the approaches applied
in the various epidemiologic studies to
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estimate PM2.5 exposure and/or to
calculate the related study-reported
mean concentration (i.e., population
weighting, trim mean approaches) can
affect those data values. More detail
related to hybrid modeling methods,
performance of the methods, and how
the reported mean concentrations
compare across approaches is provided
in section 2.3.3.2 of the PA (U.S. EPA,
2022b). The subsections below discuss
the characterization of PM2.5
concentrations based on monitoring
data (I.D.5.a) and using hybrid modeling
approaches (I.D.5.b).
a. Predicted Ambient PM2.5 and
Exposure Based on Monitored Data
Ambient concentrations of PM2.5 are
often characterized using measurements
from national monitoring networks due
to the accuracy and precision of the
measurements and the public
availability of data. For applications
requiring PM2.5 characterizations across
large areas or provide complete coverage
from the site measurements, data
interpolation and averaging techniques
(such as Average Nearest Neighbor
tools, and area-wide or populationweighted averaging of monitors) are
sometimes used (U.S. EPA, 2019a,
chapter 3).
For an area to meet the NAAQS, all
valid design values 39 in that area,
including the highest annual and 24hour values, must be at or below the
levels of the standards. Because the
monitoring network siting requirements
are specified to capture the high PM2.5
concentrations (U.S. EPA, 2022b,
section 2.2.3), areas meeting an annual
PM2.5 standard with a particular level
would be expected to have long-term
average monitored PM2.5 concentrations
(i.e., averaged across space and over
time in the area) somewhat below that
standard level. Analyses in the PA
indicate that, based on recent air quality
in U.S. CBSAs, maximum annual PM2.5
design values are often 10% to 20%
higher than annual average
concentrations (i.e., averaged across
multiple monitors in the same CBSA)
(U.S. EPA, 2022b, section 2.3.3.1,
Figures 2–28 and 2–29). This means that
the PM2.5 design value in an area is
associated with a distribution of PM2.5
concentrations in that area, and based
on monitoring siting requirements,
should represent the highest
concentration location applicable to be
monitored under the PM2.5 NAAQS.
This difference between the maximum
annual design value and the average
concentration in an area can vary,
depending on factors such as the
number of monitors, monitor siting
characteristics, and the distribution of
ambient PM2.5 concentrations. Given
that higher PM2.5 concentrations have
been reported at some near-road
monitoring sites relative to the
surrounding area (U.S. EPA, 2022b,
section 2.3.2.2.2), recent requirements
for PM2.5 monitoring at near-road
locations in large urban areas (U.S. EPA,
2022b, section 2.2.3.3) may increase the
ratios of maximum design values to
average annual design values in some
areas. Such ratios may also depend on
how the averages are calculated (i.e.,
averaged across monitors versus across
modeled grid cells, as described below
in section I.5.b). Compared to annual
design values, the analysis in the PA
indicates a more variable relationship
between maximum 24-hour PM2.5
design values and annual average
concentrations (U.S. EPA, 2022b,
section 2.3.3.1, Figure 2–29).
b. Comparison of PM2.5 Fields in
Estimating Exposure and Relative to
Design Values
Two types of hybrid approaches that
have been utilized in several key PM2.5
epidemiologic studies in the 2019 ISA
and ISA Supplement include neural
network approaches and a satellitebased method with regression of
residual PM2.5 with land-use and other
variables to improve estimates of PM2.5
concentration in the U.S. As such, the
PA further compares these two types of
approaches across various scales (e.g.,
CBSA versus nationwide), taking into
account population weighting
approaches utilized in epidemiologic
studies when estimating PM2.5 exposure
(U.S. EPA, 2022b, section 2.3.3.2.4).
Additionally, the PA assesses how
average PM2.5 concentrations computed
in epidemiologic studies using these
hybrid surfaces compare to the
maximum design values measured at
ground-based monitors. For this
assessment, the PA evaluates the
39 For the annual PM
2.5 standard, design values
are calculated as the annual arithmetic mean PM2.5
concentration, averaged over 3 years. For the 24hour standard, design values are calculated as the
98th percentile of the annual distribution of 24hour PM2.5 concentrations, averaged over three
years (appendix N of 40 CFR part 50).
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DI2019 40 and HA2020 41 hybrid
surfaces, surfaces that are used in
several of the key epidemiologic studies
in the PA. This analysis is intended to
help inform how the magnitude of the
overall study reported mean PM2.5
concentrations in epidemiologic studies
may be influenced by the approach used
to compute that mean and how that
value might compare to monitor
reported concentrations.
In estimating exposure, some studies
focus on estimating concentrations in
urban areas, while others examine the
entire U.S. or large portions of the
country. In general, the areas that are
not included in the CBSA-only analysis
tend to be more rural or less densely
populated areas, tend to have lower
PM2.5 concentrations, and likely
correspond to those locations where
monitoring data availability is limited or
nonexistent (U.S. EPA, 2022b, section
2.3.3.2.4, Figure 2–37). To evaluate the
differences in mean PM2.5
concentrations across different spatial
scales, the PA analysis compares the
DI2019 and HA2020 surfaces. At the
national scale, the two surfaces
generally produce similar average
annual PM2.5 concentrations, with the
DI2019 surface being slightly higher
compared to the HA2020 surface. The
average annual PM2.5 concentrations are
also slightly higher using the DI2019
surface compared to the HA2020 surface
when the analyses are conducted for
CBSAs. Also, regardless of which
surface is used, the average annual and
3-year average of the average annual
PM2.5 concentrations for the CBSA-only
analyses are somewhat higher than for
the nationwide analyses (4–8% higher)
(U.S. EPA, 2022b, section 2.3.3.2.4,
Table 2–5).42 Overall, these analyses
suggest that there are only slight
differences in the average PM2.5
40 This analysis includes an updated version of
the surface used in Di et al. (2016). Predictions in
Di et al. (2016) were for 2000 to 2012 using a neural
network model. The Di et al. (2019) study improved
on that effort in several ways. First, a generalized
additive model was used that accounted for
geographic variations in performance to combine
predictions from three models (neural network,
random forest, and gradient boosting) to make the
final optimal PM2.5 predictions. Second, the
datasets were updated that were used in model
training and included additional variables such as
12-km community multiscale air quality (CMAQ)
modeling as predictors. Finally, more recent years
were included in the Di et al. (2019) study.
41 The HA2020 field is based on the V4.NA.03
product available at: https://sites.wustl.edu/acag/
datasets/surface-pm2-5/. The name ‘‘HA2020’’
comes from the references for this product (Hammer
et al., 2020; van Donkelaar et al., 2019).
42 For the national scale, 3-year averages of the
average annual PM2.5 concentrations generally range
from about 5.3 mg/m3 to 8.1 mg/m3, compared to the
CBSA scale, which ranges from 5.7 mg/m3 to 8.7 mg/
m3. (U.S. EPA, 2022b, section 2.3.3.2.4, Table 2–6).
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concentrations depending on the hybrid
modeling method employed, though
including other hybrid modeling
methods in this comparison could result
in larger differences.
The PA next evaluates how the
averages of the hybrid model surfaces
compare to regulatory design values
using both the DI2019 and HA2020
surfaces and how population weighting
influences the mean PM2.5
concentration.43 As presented in the PA,
the results using the DI2019 and
HA2020 surfaces are similar for the
average annual PM2.5 concentrations, for
each 3-year period. When population
weighting is not applied, the average
annual PM2.5 concentrations generally
range from 7.0 to 8.6 mg/m3. When
population weighting is applied, the
average annual PM2.5 concentrations are
slightly higher, ranging from 8.2 to 10.2
mg/m3. As with CBSAs versus the
national comparison above, population
weighting results in a higher average
PM2.5 concentration than when
population weighting is not applied
(U.S. EPA, 2022b, section 2.3.3.2.4,
Table 2–7). For the CBSAs included in
the population weighted analyses, the
average maximum annual design values
generally range from 9.5 to 11.7 mg/m3.
The results are similar for both the
DI2019 and HA2020 surfaces and the
maximum annual PM2.5 design values
measured at the monitors are often 40%
to 50% higher than average annual
PM2.5 concentrations predicted by
hybrid modeling methods when
population weighting is not applied.
However, when population weighting is
applied, the ratio of the maximum
annual PM2.5 design values to the
predicted average annual PM2.5
concentrations are lower than when
population weighting is not applied,
with monitored design values generally
15% to 18% higher than populationweighted hybrid modeling average
annual PM2.5 concentrations (U.S. EPA,
2022b, section 2.3.3.2.4, Table 2–7).
6. Background PM
In this reconsideration, background
PM is defined as all particles that are
formed by sources or processes that
cannot be influenced by actions within
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43 For
this analysis, the PA includes CBSAs with
three or more valid design values for the 3-year
period. The regulatory design values for the CBSAs
were calculated for each 3-year period for the
CBSAs with 3 or more design values in each of the
3-year periods. Using the maximum design value
for each CBSA and by each 3-year period, the ratio
of maximum design values to modeled average
annual PM2.5 concentrations were calculated, for
each 3-year period. More details about the
analytical methods used for this analysis are
described in section A.6 of Appendix A in the PA
(U.S. EPA, 2022b).
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the jurisdiction of concern. U.S.
background PM is defined as any PM
formed from emissions other than U.S.
anthropogenic (i.e., manmade)
emissions. Potential sources of U.S.
background PM include both natural
sources (i.e., PM that would exist in the
absence of any anthropogenic emissions
of PM or PM precursors) and
transboundary sources originating
outside U.S. borders. Background PM is
discussed in more detail in the PA (U.S.
EPA, 2022b, section 2.4). At annual and
national scales, estimated background
PM concentrations in the U.S. are small
compared to contributions from
domestic anthropogenic sources.44 For
example, based on zero-out modeling in
the last review of the PM NAAQS,
annual background PM2.5
concentrations were estimated to range
from 0.5–3 mg/m3 across the sites
examined. In addition, speciated
monitoring data from IMPROVE sites
can provide some insights into how
contributions from different sources,
including sources of background PM,
may have changed over time. Such data
suggests the estimates of background
concentrations using speciated
monitoring data from IMPROVE
monitors are around 1–3 mg/m3 and
have not changed significantly since the
2012 review. Contributions to
background PM in the U.S. result
mainly from sources within North
America. Contributions from
intercontinental events have also been
documented (e.g., transport from dust
storms occurring in deserts in North
Africa and Asia), but these events are
less frequent and represent a relatively
small fraction of background PM in
most of the U.S. (U.S. EPA, 2022b,
section 2.4).
II. Rationale for Proposed Decisions on
the Primary PM2.5 Standards
This section presents the rationale for
the Administrator’s proposed decision
to revise the primary annual PM2.5
standard and retain the primary 24-hour
PM2.5 standard. This rationale is based
on a thorough review of the scientific
evidence generally published through
44 Sources that contribute to natural background
PM include dust from the wind erosion of natural
surfaces, sea salt, wildland fires, primary biological
aerosol particles such as bacteria and pollen,
oxidation of biogenic hydrocarbons such as
isoprene and terpenes to produce secondary organic
aerosols (SOA), and geogenic sources such as
sulfate formed from volcanic production of SO2 and
oceanic production of dimethyl-sulfide (U.S. EPA,
2022b, section 2.4). While most of these sources
release or contribute predominantly to fine aerosol,
some sources including windblown dust, and sea
salt also produce particles in the coarse size range
(U.S. EPA, 2019a, section 2.3.3).
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January 2018,45 as presented in the 2019
ISA (U.S. EPA, 2019a), on the human
health effects of PM2.5 associated with
long- and short-term exposures 46 to
PM2.5 in the ambient air. Additionally,
this rationale is based on a thorough
evaluation of some studies that became
available after the literature cutoff date
of the 2019 ISA, as evaluated in the ISA
Supplement, that could either further
inform the adequacy of the current PM
NAAQS or address key scientific topics
that have evolved since the literature
cutoff date for the 2019 ISA, generally
through March 2021 (U.S. EPA,
2022b).47 The Administrator’s rationale
also takes into account: (1) the PA
evaluation of the policy-relevant
information in the 2019 ISA and ISA
Supplement and presentation of
quantitative analyses of air quality and
health risks; (2) CASAC advice and
recommendations, as reflected in
discussions of the drafts of the ISA
Supplement and PA at public meetings
and in the CASAC’s letters to the
Administrator; and (3) public comments
received during the development of
these documents.
In presenting the rationale for the
Administrator’s proposed decisions and
its foundations, section II.A provides
background and introductory
information for this reconsideration of
the primary PM2.5 standards. It includes
background on the 2020 final decision
to retain the primary PM2.5 standards
(section II.A.1) and also describes the
general approach for this
reconsideration (section II.A.2). Section
II.B summarizes the key aspects of the
currently available health effects
evidence, focusing on consideration of
45 In addition to the 2020 review’s opening ‘‘call
for information’’ (79 FR 71764, December 3, 2014),
the 2019 ISA identified and evaluated studies and
reports that have undergone scientific peer review
and were published or accepted for publication
between January 1, 2009, through approximately
January 2018 (U.S. EPA, 2019a, p. ES–2). References
that are cited in the 2019 ISA, the references that
were considered for inclusion but not cited, and
electronic links to bibliographic information and
abstracts can be found at: https://hero.epa.gov/hero/
particulate-matter.
46 Short-term exposures are defined as those
exposures occurring over hours up to 1 month,
whereas long-term exposures are defined as those
exposures occurring over 1 month to years (U.S.
EPA, 2019a, section P.3.1).
47 The ISA Supplement represents an evaluation
of recent studies that are of greatest policy
relevance to the reconsideration of the 2020 final
decision on the PM NAAQS. Specifically, the ISA
Supplement focuses on studies of health effects for
which the evidence in the 2019 ISA supported a
‘‘causal relationship’’ (i.e., short- and long-term
PM2.5 exposure and mortality and cardiovascular
effects) because those were the health effects that
were most useful in informing conclusions in the
2020 PA. The ISA Supplement does not include an
evaluation of studies for other PM2.5-related health
effects (U.S. EPA, 2022b).
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the key policy-relevant aspects. Section
II.C summarizes the risk information for
this reconsideration, drawing on the
quantitative analyses for PM2.5,
presented in the PA. Section II.D
presents the Administrator’s proposed
conclusions on the current primary
annual and 24-hour PM2.5 standards
(section II.D.3), drawing on both the
evidence-based and risk-based
considerations (section II.D.2) and
advice from the CASAC (section II.D.1).
A. General Approach
This reconsideration of the 2020 final
decision on the primary PM2.5 standards
relies on using the EPA’s assessment of
the current scientific evidence and
associated quantitative analyses to
inform the Administrator’s judgment
regarding primary PM2.5 standards that
protect public health with an adequate
margin of safety. The EPA’s assessments
are primarily documented in the 2019
ISA, ISA Supplement, and PA, all of
which have received CASAC review and
public comment (83 FR 53471, October
23, 2018; 83 FR 55529, November 6,
2018; 85 FR 4655, January 27, 2020; 86
FR 52673, September 22, 2021; 86 FR
54186, September 30, 2021; 86 FR
56263, October 8, 2021; 87 FR 958,
January 7, 2022; 87 FR 22207, April 14,
2022; 87 FR 31965, May 26, 2022). In
bridging the gap between the scientific
assessments of the 2019 ISA and ISA
Supplement and the judgments required
of the Administrator in determining
whether the current standards provide
the requisite public health protection,
the PA evaluates policy implications of
the evaluation of the current evidence in
the 2019 ISA and ISA Supplement, and
the risk information documented in the
PA. In evaluating the public health
protection afforded by the current
standards, the four basic elements of the
NAAQS (indicator, averaging time,
level, and form) are considered
collectively.
The final decision on the adequacy of
the current primary PM2.5 standards is a
public health policy judgment to be
made by the Administrator. In reaching
conclusions with regard to the
standards, the decision will draw on the
scientific information and analyses
about health effects and population
risks, as well as judgments about how to
consider the range and magnitude of
uncertainties that are inherent in the
scientific evidence and analyses. This
approach is based on the recognition
that the available health effects evidence
generally reflects a continuum,
consisting of levels at which scientists
generally agree that health effects are
likely to occur, through lower levels at
which the likelihood and magnitude of
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the response become increasingly
uncertain. This approach is consistent
with the requirements of the NAAQS
provisions of the Clean Air Act and with
how the EPA and the courts have
historically interpreted the Act
(summarized in section I.A above).
These provisions require the
Administrator to establish primary
standards that, in the judgment of the
Administrator, are requisite to protect
public health with an adequate margin
of safety. In so doing, the Administrator
seeks to establish standards that are
neither more nor less stringent than
necessary for this purpose. The Act does
not require that primary standards be set
at a zero-risk level, but rather at a level
that avoids unacceptable risks to public
health, including the health of sensitive
groups.48
The subsections below provide
background and introductory
information. Background on the 2020
decision to retain the current standards,
including the rationale for that decision,
is summarized in section II.A.1. This is
followed, in section II.A.2, by an
overview of the general approach for the
reconsideration of the 2020 final
decision. Following this introductory
section and subsections, the subsequent
sections summarize current information
and analyses, including that newly
available in this reconsideration. The
Administrator’s proposed conclusions
on the primary PM2.5 standards, based
on the current information, are provided
in section II.D.3.
1. Background on the Current Standards
The current primary PM2.5 standards
were retained in 2020 based on the
scientific evidence and quantitative risk
analyses available at that time, as well
as the Administrator’s judgments
regarding the available scientific
information, the appropriate degree of
public health protection for the
standards, and the available risk
information regarding the exposures and
risk that may be allowed by the current
standards (85 FR 82718, December 18,
2020). With the 2020 final decision, the
EPA retained the primary 24-hour PM2.5
standard, with its level of 35 mg/m3, and
the primary annual PM2.5 standard, with
its level of 12.0 mg/m3, this decision was
informed by the scientific evidence
evaluated in the 2019 ISA, the evidence
and quantitative risk information in the
2020 PA, the advice and
recommendations of the CASAC, and
48 As noted in section I.A above, the legislative
history describes such protection for the sensitive
group of individuals and not for a single person in
the sensitive group (see S. Rep. No. 91–1196, 91st
Cong, 2d Sess. 10 [1970]).
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public comments on the proposed
decision (85 FR 24094, April 30, 2020).
The health effects evidence base
available in the 2020 review included
extensive evidence from previous
reviews as well as the evidence that had
emerged since the prior review had been
completed in 2012. This evidence base,
spanning several decades, documents
the relationship between short- and
long-term PM2.5 exposure and mortality
or serious morbidity effects. The
evidence available in the 2019 ISA
reaffirmed, and in some cases
strengthened, the conclusions from the
2009 ISA regarding the health effects of
PM2.5 exposures (U.S. EPA, 2009a).
Much of the evidence came from
epidemiologic studies conducted in
North America, Europe, or Asia
examining short-term and long-term
exposures that demonstrated generally
positive, and often statistically
significant, PM2.5 health effect
associations with a range of outcomes
including non-accidental,
cardiovascular, or respiratory mortality;
cardiovascular or respiratory
hospitalizations or emergency
department visits; and other mortality/
morbidity outcomes (e.g., lung cancer
mortality or incidence, asthma
development). Experimental evidence,
as well as evidence from panel studies,
strengthened support for potential
biological pathways through which
PM2.5 exposures could lead to health
effects reported in many populationbased epidemiologic studies, including
support for pathways that could lead to
cardiovascular, respiratory, nervous
system, and cancer-related effects.
Based on this evidence, the 2019 ISA
concludes there to be a causal
relationship between long- and shortterm PM2.5 exposure and mortality and
cardiovascular effects, as well as likely
to be causal relationships between longand short-term PM2.5 exposures and
respiratory effects, and between longterm PM2.5 exposures and cancer and
nervous system effects (U.S. EPA,
2019a, section 1.7).
Epidemiologic studies reported PM2.5
health effect associations with mortality
and/or morbidity across multiple U.S.
cities and in diverse populations,
including in studies examining
populations and lifestages that may be
at increased risk of experiencing a
PM2.5-related health effect (e.g., older
adults, children). The 2019 ISA cited
extensive evidence indicating that ‘‘both
the general population as well as
specific populations and lifestages are at
risk for PM2.5-related health effects’’
(U.S. EPA, 2019a, p. 12–1). Some of the
evidence that supported conclusions on
at-risk populations and lifestages also
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contributed to the conclusions of causal
and likely to be causal relationships
within the 2019 ISA, including:
• PM2.5-related mortality and
cardiovascular effects in older adults
(U.S. EPA, 2019a, sections 11.1, 11.2,
6.1, and 6.2);
• PM2.5-related cardiovascular effects
in people with pre-existing
cardiovascular disease (U.S. EPA,
2019a, section 6.1);
• PM2.5-related respiratory effects in
people with pre-existing respiratory
disease, particularly asthma (U.S. EPA,
2019a, section 5.1);
• PM2.5-related impairments in lung
function growth and asthma
development in children (U.S. EPA,
2019a, sections 5.1, 5.2, and 12.5.1.1).
The 2019 ISA also noted that
stratified analyses (i.e., analyses that
allow for the comparison of PM-related
health effects across different
populations) provided strong evidence
for racial and ethnic differences in PM2.5
exposures and PM2.5-related health risk.
Such analyses indicated that certain
racial and ethnic groups, specifically
Hispanic and non-Hispanic Black
populations have higher PM2.5
exposures than non-Hispanic White
populations, thus contributing to risk of
adverse PM2.5-related health effects in
minority populations (U.S. EPA, 2019a,
section 12.5.4). Stratified analyses
focusing on other groups also suggested
that populations with pre-existing
cardiovascular or respiratory disease,
populations that are overweight or
obese, populations that have particular
genetic variants, and populations that
are of low socioeconomic status (SES)
could be at increased risk for PM2.5related adverse health effects (U.S. EPA,
2019a, chapter 12).
The risk information available in the
2020 review included risk estimates for
air quality conditions just meeting the
existing primary PM2.5 standards, and
also for air quality conditions just
meeting potential alternative standards.
The general approach to estimating
PM2.5-associated health risks combined
concentration-response (C–R) functions
from epidemiologic studies with modelbased PM2.5 air quality surfaces,
baseline health incidence data, and
population demographics for 47 urban
areas (U.S. EPA, 2022b, section 3.3,
Figure 3–10, Appendix C). The risk
assessment estimated that the existing
primary PM2.5 standards could allow a
substantial number of PM2.5-associated
deaths in the U.S. Uncertainty in risk
estimates (e.g., in the size of risk
estimates) can result from a number of
factors, including assumptions about the
shape of the C–R relationship with
mortality at low ambient PM2.5
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concentrations, the potential for
confounding and/or exposure
measurement error, and the methods
used to adjust PM2.5 air quality.
Consistent with the general approach
routinely employed in NAAQS reviews,
the initial consideration in the 2020
review of the primary PM2.5 standards
was with regard to the adequacy of the
protection provided by the existing
standards. Key aspects of the
consideration are summarized in section
II.A.1.a below.
a. Considerations Regarding the
Adequacy of the Existing Standards in
the 2020 Review
With the 2020 final decision, the EPA
retained the primary 24-hour PM2.5
standard, with its level of 35 mg/m3, and
the primary annual PM2.5 standard, with
its level of 12.0 mg/m3. The
Administrator’s conclusions regarding
the adequacy of the primary PM2.5
standards at the time of the 2020 review
was based on consideration of the
evidence, analyses and conclusions
contained in the 2019 ISA; the
quantitative risk assessment in the 2020
PA; advice from the CASAC; and public
comments. Key considerations
informing the Administrator’s decision
to retain the standards that were
promulgated in the 2012 review are
summarized below.
As an initial matter, the Administrator
considered the range of scientific
evidence evaluating these effects,
including studies of at-risk populations,
to inform his review of the primary
PM2.5 standards, placing the greatest
weight on evidence of effects for which
the 2019 ISA determined there to be a
causal or likely to be causal relationship
with long- and short-term PM2.5
exposures (85 FR 82714–82715,
December 18, 2020).
With regard to indicator, the
Administrator recognized that,
consistent with the evidence available
in prior reviews, the scientific evidence
in the 2020 review continued to provide
strong support for health effects
following short- and long-term PM2.5
exposures. He noted the 2020 PA
conclusions that the information
continued to support the PM2.5 massbased indicator and remained too
limited to support a distinct standard
for any specific PM2.5 component or
group of components, and too limited to
support a distinct standard for the
ultrafine fraction. Thus, the
Administrator concluded that it was
appropriate to retain PM2.5 as the
indicator for the primary standards for
fine particles (85 FR 82715, December
18, 2020).
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With respect to averaging time and
form, the Administrator noted that the
scientific evidence continued to provide
strong support for health effects
associations with both long-term (e.g.,
annual or multi-year) and short-term
(e.g., mostly 24-hour) exposures to
PM2.5, consistent with the conclusions
in the 2020 PA. In the 2019 ISA,
epidemiologic and controlled human
exposure studies examined a variety of
PM2.5 exposure durations.
Epidemiologic studies continued to
provide strong support for health effects
associated with short-term PM2.5
exposures based on 24-hour PM2.5
averaging periods, and the EPA noted
that associations with sub-daily
estimates are less consistent and, in
some cases, smaller in magnitude (U.S.
EPA, 2019a, section 1.5.2.1; U.S. EPA,
2020a, section 3.5.2.2). In addition,
controlled human exposure and panelbased studies of sub-daily exposures
typically examined subclinical effects,
rather than the more serious populationlevel effects that have been reported to
be associated with 24-hour exposures
(e.g., mortality, hospitalizations). Taken
together, the 2019 ISA concludes that
epidemiologic studies did not indicate
that sub-daily averaging periods were
more closely associated with health
effects than the 24-hour average
exposure metric (U.S. EPA, 2019a,
section 1.5.2.1). Additionally, while
controlled human exposure studies
provided consistent evidence for
cardiovascular effects following PM2.5
exposures for less than 24 hours (i.e., <
30 minutes to 5 hours), exposure
concentrations in the studies were wellabove the ambient concentrations
typically measured in locations meeting
the existing standards (U.S. EPA, 2020a,
section 3.2.3.1). Thus, these studies also
did not suggest the need for additional
protection against sub-daily PM2.5
exposures (U.S. EPA, 2020a, section
3.5.2.2). Therefore, the Administrator
judged that the 24-hour averaging time
remained appropriate (85 FR 82715,
December 18, 2020).
With regard to the form of the 24-hour
standard (98th percentile, averaged over
three years), the Administrator noted
that epidemiologic studies continued to
provide strong support for health effect
associations with short-term (e.g.,
mostly 24-hour) PM2.5 exposures (U.S.
EPA, 2020a, section 3.5.2.3) and that
controlled human exposure studies
provided evidence for health effects
following single short-term ‘‘peak’’
PM2.5 exposures. Thus, the evidence
supported retaining a standard focused
on providing supplemental protection
against short-term peak exposures and
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supported a 98th percentile form for a
24-hour standard. The Administrator
further noted that this form also
provided an appropriate balance
between limiting the occurrence of peak
24-hour PM2.5 concentrations and
identifying a stable target for risk
management programs (U.S. EPA,
2020a, section 3.5.2.3). As such, the
Administrator concluded that the
available information supported
retaining the form and averaging time of
the current 24-hour standard (98th
percentile, averaged over three years)
and annual standard (annual average,
averaged over three years) (85 FR 82715,
December 18, 2020).
With regard to the level of the
standards, in reaching his final decision,
the Administrator considered the large
body of evidence presented and
assessed in the 2019 ISA (U.S. EPA,
2019a), the policy-relevant and riskbased conclusions and rationales as
presented in the 2020 PA (U.S. EPA,
2020a), advice from the CASAC, and
public comments. In particular, in
considering the 2019 ISA and 2020 PA,
he considered key epidemiologic
studies that evaluated associations
between PM2.5 air quality distributions
and mortality and morbidity, including
key accountability studies; the
availability of experimental studies to
support biological plausibility;
controlled human exposure studies
examining effects following short-term
PM2.5 exposures; air quality analyses;
and the important uncertainties and
limitations associated with the
information (85 FR 82715, December 18,
2020).
As an initial matter, the Administrator
considered the protection afforded by
both the annual and 24-hour standards
together against long- and short-term
PM2.5 exposures and health effects. The
Administrator recognized that the
annual standard was most effective in
controlling ‘‘typical’’ PM2.5
concentrations near the middle of the
air quality distribution (i.e., around the
mean of the distribution), but also
provided some control over short-term
peak PM2.5 concentrations. On the other
hand, the 24-hour standard, with its
98th percentile form, was most effective
at limiting peak 24-hour PM2.5
concentrations, but in doing so also had
an effect on annual average PM2.5
concentrations. Thus, while either
standard could be viewed as providing
some measure of protection against both
average exposures and peak exposures,
the 24-hour and annual standards were
not expected to be equally effective at
limiting both types of exposures. Thus,
consistent with previous reviews, the
Administrator’s consideration of the
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public health protection provided by the
existing primary PM2.5 standards was
based on his consideration of the
combination of the annual and 24-hour
standards. Specifically, he recognized
that the annual standard was more
likely to appropriately limit the
‘‘typical’’ daily and annual exposures
that are most strongly associated with
the health effects observed in
epidemiologic studies. The
Administrator concluded that an annual
standard (as the arithmetic mean,
averaged over three years) remained
appropriate for targeting protection
against the annual and daily PM2.5
exposures around the middle portion of
the PM2.5 air quality distribution.
Further, recognizing that the 24-hour
standard (with its 98th percentile form)
was more directly tied to short-term
peak PM2.5 concentrations, and more
likely to appropriately limit exposures
to such concentrations, the
Administrator concluded that the
current 24-hour standard (with its 98th
percentile form, averaged over three
years) remained appropriate to provide
a balance between limiting the
occurrence of peak 24-hour PM2.5
concentrations and identifying a stable
target for risk management programs.
However, the Administrator recognized
that changes in PM2.5 air quality to meet
an annual standard would likely result
not only in lower short- and long-term
PM2.5 concentrations near the middle of
the air quality distribution, but also in
fewer and lower short-term peak PM2.5
concentrations. The Administrator
further recognized that changes in air
quality to meet a 24-hour standard, with
a 98th percentile form, would result not
only in fewer and lower peak 24-hour
PM2.5 concentrations, but also in lower
annual average PM2.5 concentrations (85
FR 82715–82716, December 18, 2020).
Thus, in considering the adequacy of
the 24-hour standard, the Administrator
noted the importance of considering
whether additional protection was
needed against short-term exposures to
peak PM2.5 concentrations. In examining
the scientific evidence, he noted the
limited utility of the animal
toxicological studies in directly
informing conclusions on the
appropriate level of the standard given
the uncertainty in extrapolating from
effects in animals to those in human
populations. The Administrator noted
that controlled human exposure studies
provided evidence for health effects
following single, short-term PM2.5
exposures that corresponded best to
exposures that might be experienced in
the upper end of the PM2.5 air quality
distribution in the U.S. (i.e., ‘‘peak’’
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concentrations). However, most of these
studies examined exposure
concentrations considerably higher than
are typically measured in areas meeting
the standards (U.S. EPA, 2020a, section
3.2.3.1). In particular, controlled human
exposure studies often reported
statistically significant effects on one or
more indicators of cardiovascular
function following 2-hour exposures to
PM2.5 concentrations at and above 120
mg/m3 (at and above 149 mg/m3 for
vascular impairment, the effect shown
to be most consistent across studies). To
provide insight into what these studies
may indicate regarding the primary
PM2.5 standards, the 2020 PA (U.S. EPA,
2020a, p. 3–49) noted that 2-hour
ambient concentrations of PM2.5 at
monitoring sites meeting the current
standards almost never exceeded 32 mg/
m3. In fact, even the extreme upper end
of the distribution of 2-hour PM2.5
concentrations at sites meeting the
primary PM2.5 standards remained wellbelow the PM2.5 exposure
concentrations consistently shown in
controlled human exposure studies to
elicit effects (i.e., 99.9th percentile of 2hour concentrations at these sites is 68
mg/m3 during the warm season). Thus,
the available experimental evidence did
not indicate the need for additional
protection against exposures to peak
PM2.5 concentrations, beyond the
protection provided by the combination
of the 24-hour and the annual standards
(U.S. EPA, 2020a, section 3.2.3.1; 85 FR
82716, December 18, 2020).
With respect to the epidemiologic
evidence, the Administrator noted that
the studies did not indicate that
associations in those studies were
strongly influenced by exposures to
peak concentrations in the air quality
distribution and thus did not indicate
the need for additional protection
against short-term exposures to peak
PM2.5 concentrations (U.S. EPA, 2020a,
section 3.5.1 The Administrator noted
that this was consistent with CASAC
consensus support for retaining the
current 24-hour standard. Thus, the
Administrator concluded that the 24hour standard with its level of 35 mg/m3
was adequate to provide supplemental
protection (i.e., beyond that provided by
the annual standard alone) against
short-term exposures to peak PM2.5
concentrations (85 FR 82716, December
18, 2020).
With regard to the level of the annual
standard, the Administrator recognized
that the annual standard, with its form
based on the arithmetic mean
concentration, was most appropriately
meant to limit the ‘‘typical’’ daily and
annual exposures that were most
strongly associated with the health
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effects observed in epidemiologic
studies. However, the Administrator
also noted that while epidemiologic
studies examined associations between
distributions of PM2.5 air quality and
health outcomes, they did not identify
particular PM2.5 exposures that cause
effects and thus, they could not alone
identify a specific level at which the
standard should be set, as such a
determination necessarily required the
Administrator’s judgment. Thus,
consistent with the approaches in
previous NAAQS reviews, the
Administrator recognized that any
approach that used epidemiologic
information in reaching decisions on
what standards are appropriate
necessarily required judgments about
how to translate the information from
the epidemiologic studies into a basis
for appropriate standards. This
approach included consideration of the
uncertainties in the reported
associations between daily or annual
average PM2.5 exposures and mortality
or morbidity in the epidemiologic
studies. Such an approach is consistent
with setting standards that are neither
more nor less stringent than necessary,
recognizing that a zero-risk standard is
not required by the Clean Air Act (CAA)
(85 FR 82716, December 18, 2020).
The Administrator emphasized
uncertainties and limitations that were
present in epidemiologic studies in
previous reviews and persisted in the
2020 review. These uncertainties
included exposure measurement error,
potential confounding by copollutants,
increasing uncertainty of associations at
lower PM2.5 concentrations, and
heterogeneity of effects across different
cities or regions (85 FR 82716,
December 18, 2020). The Administrator
also noted the advice given by the
CASAC on this matter. As described in
section I.C.5 above, the CASAC did not
reach consensus on the adequacy of the
primary annual PM2.5 standard. ‘‘Some
CASAC members’’ expressed support
for retaining the primary annual PM2.5
standard while ‘‘other members’’
expressed support for revising that
standard in order to increase public
health protection (Cox, 2019a, p. 1 of
consensus letter). The CASAC members
who supported retaining the annual
standard expressed their concerns with
the epidemiologic studies, asserting that
these studies did not provide a
sufficient basis for revising the existing
standards. They also identified several
key concerns regarding the associations
reported in epidemiologic studies and
concluded that ‘‘while the data on
associations should certainly be
carefully considered, this data should
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not be interpreted more strongly than
warranted based on its methodological
limitations’’ (Cox, 2019a, p. 8 consensus
responses).
Taking into consideration the views
expressed by the CASAC members who
supported retaining the annual
standard, the Administrator recognized
that epidemiologic studies examined
associations between distributions of
PM2.5 air quality and health outcomes,
and they did not identify particular
PM2.5 exposures that cause effects (U.S.
EPA, 2020a, section 3.1.2). While the
Administrator remained concerned
about placing too much weight on
epidemiologic studies to inform
conclusions on the adequacy of the
primary standards, he noted the
approach to considering such studies in
the 2012 review. In the 2012 review, it
was noted that the evidence of an
association in any epidemiologic study
was ‘‘strongest at and around the longterm average where the data in the study
are most concentrated’’ (78 FR 3140,
January 15, 2013). In considering the
characterization of epidemiologic
studies, the Administrator viewed that
when assessing the mean concentrations
of the key short-term and long-term
epidemiologic studies in the U.S. that
use ground-based monitoring (i.e., those
studies where the mean is most directly
comparable to the current annual
standard), the majority of studies had
mean concentrations at or above the
level of the existing annual standard,
with the mean of the study-reported
means or medians equal to 13.5 mg/m3,
a concentration level above the existing
level of the primary annual standard of
12 mg/m3. The Administrator further
noted his caution in directly comparing
the reported study mean values to the
standard level given that study-reported
mean concentrations, by design, are
generally lower than the design value of
the highest monitor in an area, which
determines compliance. In the 2020 PA,
analyses of recent air quality in U.S.
CBSAs indicated that maximum annual
PM2.5 design values for a given threeyear period were often 10% to 20%
higher than average monitored
concentrations (i.e., averaged across
multiple monitors in the same CBSA)
(U.S. EPA, 2020a, Appendix B, section
B.7). He further noted his concern in
placing too much weight on any one
epidemiologic study but instead judged
that it was more appropriate to focus on
the body of studies together and
therefore noted the calculation of the
mean of study-reported means (or
medians). Thus, while the
Administrator was cautious in placing
too much weight on the epidemiologic
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evidence alone, he noted that: (1) the
reported mean concentration in the
majority of the key U.S. epidemiologic
studies using ground-based monitoring
data were above the level of the existing
annual standard; (2) the mean of the
reported study means (or medians) (i.e.,
13.5 mg/m3) was above the level of the
current standard; 49 (3) air quality
analyses showed the study means to be
lower than their corresponding design
values by 10–20%; and (4) these
analyses must be considered in light of
uncertainties inherent in the
epidemiologic evidence. When taken
together, the Administrator judged that,
even if it were appropriate to place more
weight on the epidemiologic evidence,
this information did not call into
question the adequacy of the current
standards (85 FR 82716–82717,
December 18, 2020).
In addition to the evidence, the
Administrator also considered the
potential implications of the risk
assessment. He noted that all risk
assessments have limitations and that
he remained concerned about the
uncertainties in the underlying
epidemiologic data used in the risk
assessment. The Administrator also
noted that in previous reviews, these
uncertainties and limitations have often
resulted in less weight being placed on
quantitative estimates of risk than on
the underlying scientific evidence itself
(e.g., 78 FR 3086, 3098–99, January 15,
2013). These uncertainties and
limitations included uncertainty in the
shapes of C–R functions, particularly at
low concentrations; uncertainties in the
methods used to adjust air quality; and
uncertainty in estimating risks for
populations, locations and air quality
distributions different from those
examined in the underlying
epidemiologic study (U.S. EPA, 2020a,
section 3.3.2.4). Additionally, the
Administrator noted similar concern
expressed by some members of the
CASAC who support retaining the
existing standards; they highlighted
similar uncertainties and limitations in
the risk assessment (Cox, 2019b). In
light of all of this, the Administrator
judged it appropriate to place little
weight on quantitative estimates of
PM2.5-associated mortality risk in
reaching conclusions about the level of
the primary PM2.5 standards (85 FR
82717, December 18, 2020).
The Administrator additionally
considered an emerging body of
evidence from accountability studies
that examined past reductions in
49 The median of the study-reported mean (or
median) PM2.5 concentrations is 13.3 mg/m3, which
was also above the level of the existing standard.
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ambient PM2.5 and the degree to which
those reductions resulted in public
health improvements. While the
Administrator agreed with public
commenters that well-designed and
conducted accountability studies can be
informative, he viewed the
interpretation of such studies in the
context of the primary PM2.5 standards
as complicated by the fact that some of
the available studies had not evaluated
PM2.5 specifically (e.g., as opposed to
PM10 or total suspended particulates),
did not show changes in PM2.5 air
quality, or had not been able to
disentangle health impacts of the
interventions from background trends in
health (U.S. EPA, 2020a, section 3.5.1).
He further recognized that the small
number of available studies that did
report public health improvements
following past declines in ambient PM2.5
had not examined air quality meeting
the existing standards (U.S. EPA, 2020a,
Table 3–3). This included U.S. studies
that reported increased life expectancy,
decreased mortality, and decreased
respiratory effects following past
declines in ambient PM2.5
concentrations. Such studies examined
‘‘starting’’ annual average PM2.5
concentrations (i.e., prior to the
reductions being evaluated) ranging
from about 13.2 to >20 mg/m3 (i.e., U.S.
EPA, 2020a, Table 3–3). Given the lack
of available accountability studies
reporting public health improvements
attributable to reductions in ambient
PM2.5 in locations meeting the existing
standards, together with his broader
concerns regarding the lack of
experimental studies examining PM2.5
exposures typical of areas meeting the
existing standards, the Administrator
judged that there was considerable
uncertainty in the potential for
increased public health protection from
further reductions in ambient PM2.5
concentrations beyond those achieved
under the existing primary PM2.5
standards (85 FR 82717, December 18,
2020).
When the above considerations were
taken together, the Administrator
concluded that the scientific evidence
assessed in the 2019 ISA, together with
the analyses in the 2020 PA based on
that evidence and consideration of
CASAC advice and public comments,
did not call into question the adequacy
of the public health protection provided
by the existing annual and 24-hour
PM2.5 standards. In particular, the
Administrator judged that there was
considerable uncertainty in the
potential for additional public health
improvements from reducing ambient
PM2.5 concentrations below the
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concentrations achieved under the
existing primary standards and that,
therefore, standards more stringent than
the existing standards (e.g., with lower
levels) were not supported. That is, he
judged that more stringent standards
would be more than requisite to protect
the public health with an adequate
margin of safety. This judgment
reflected the Administrator’s
consideration of the uncertainties in the
potential implications of the lower end
of the air quality distributions from the
epidemiologic studies due in part to the
lack of supporting evidence from
experimental studies and retrospective
accountability studies conducted at
PM2.5 concentrations meeting the
existing standards (85 FR 82717,
December 18, 2020).
In reaching this conclusion, the
Administrator judged that the existing
standards provided an adequate margin
of safety. With respect to the annual
standard, the level of 12 mg/m3 was
below the lowest ‘‘starting’’
concentration (i.e., 13.2 mg/m3) in the
available accountability studies that
showed public health improvements
attributable to reductions in ambient
PM2.5. In addition, while the
Administrator placed less weight on the
epidemiologic evidence for selecting a
standard, he noted that the level of the
annual standard was below the reported
mean (and median) concentrations in
the majority of the key U.S.
epidemiologic studies using groundbased monitoring data (noting that these
means tend to be 10–20% lower than
their corresponding area design values
which is the more relevant metric when
considering the level of the standard)
and below the mean of the reported
means (or medians) of these studies (i.e.,
13.5 mg/m3). In addition, the
Administrator recognized that
concentrations in areas meeting the
existing 24-hour and annual standards
remained well-below the PM2.5
exposure concentrations consistently
shown to elicit effects in human
exposure studies (85 FR 82717–82718,
December 18, 2020).
In addition, based on the
Administrator’s review of the science,
including controlled human exposure
studies examining effects following
short-term PM2.5 exposures, the
epidemiologic studies, and
accountability studies conducted at
levels just above the existing annual
standard, he judged that the degree of
public health protection provided by the
existing annual standard is not greater
than warranted. This judgment, together
with the fact that no CASAC member
expressed support for a less stringent
standard, led the Administrator to
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conclude that standards less stringent
than the existing standards (e.g., with
higher levels) were also not supported
(85 FR 82718, December 18, 2020).
In reaching his final decision, the
Administrator concluded that the
scientific evidence and technical
information continued to support the
existing annual and 24-hour PM2.5
standards. This conclusion reflected the
Administrator’s view that there were
important limitations and uncertainties
that remained in the evidence. The
Administrator concluded that these
limitations contributed to considerable
uncertainty regarding the potential
public health implications of revising
the existing primary PM2.5 standards.
Given this uncertainty, and noting the
advice from some CASAC members, he
concluded that the primary PM2.5
standards, including the indicators
(PM2.5), averaging times (annual and 24hour), forms (arithmetic mean and 98th
percentile, averaged over three years)
and levels (12.0 mg/m3, 35 mg/m3), when
taken together, remained requisite to
protect the public health. Therefore, in
the 2020 review, the Administrator
reached the conclusion that the primary
24-hour and annual PM2.5 standards,
together, were requisite to protect public
health from fine particles with an
adequate margin of safety, including the
health of at-risk populations, and
retained the standards, without revision
(85 FR 82718, December 18, 2020).
2. General Approach and Key Issues in
This Reconsideration of the 2020 Final
Decision
To evaluate whether it is appropriate
to consider retaining the current
primary PM2.5 standards, or whether
consideration of revision is appropriate,
the EPA has adopted an approach in
this reconsideration that builds upon
the general approach used in past
reviews. This includes the substantial
assessments and evaluations performed
in those reviews, and also takes into
account the more recent scientific
evidence and risk information now
available to inform understanding of the
key policy-relevant issues in the
reconsideration. As summarized above,
the Administrator’s decisions in the
2020 review were based on an
integration of PM health effects
information with the judgments on the
adversity and public health significance
of key health effects, policy judgments
as to when the standard is requisite to
protect public health with an adequate
margin of safety, and consideration of
CASAC advice and public comments.
Similarly, in this reconsideration, we
draw on the current evidence and
quantitative assessments of exposure
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along with controlled human exposure
studies associated with cardiovascular
effects at near ambient concentrations,
were considered to be of greatest utility
in informing the Administrator’s
conclusions on the adequacy of the
current primary PM2.5 standards. While
the ISA Supplement does not include
information for health effects other than
mortality and cardiovascular effects, the
scientific evidence for other health
effect categories is evaluated in the 2019
ISA, which in combination with the ISA
Supplement represents the complete
scientific record for the reconsideration
of the 2020 final decision.
The ISA Supplement also assessed
accountability studies because these
types of epidemiologic studies were part
of the body of evidence that was a focus
of the 2020 review. Accountability
studies inform our understanding of the
potential for public health
improvements as ambient PM2.5
concentrations have declined over time.
Further, the ISA Supplement considered
studies that employed statistical
B. Overview of the Health Effects
approaches that attempt to more
Evidence
extensively account for confounders and
The information summarized here is
are more robust to model
an overview of the policy-relevant
misspecification (i.e., used alternative
aspects of the health effects evidence
methods for confounder control),50
available in this reconsideration; the
given that such studies were highlighted
assessment of this evidence is
by the CASAC and identified in public
documented in the 2019 ISA and ISA
comments in the 2020 review. Since the
Supplement and its policy implications
literature cutoff date for the 2019 ISA,
are further discussed in the PA. While
multiple accountability studies and
the 2019 ISA provides the broad
studies that employ alternative methods
scientific foundation for this
for confounder control have become
reconsideration, additional literature
available for consideration in the ISA
has become available since the cutoff
Supplement and, subsequently, in this
date of the 2019 ISA that expands the
reconsideration.
body of evidence related to mortality
The ISA Supplement also considered
and cardiovascular effects for both
recent
health effects evidence that
short- and long-term PM2.5 exposure that
addresses key scientific issues where
can inform the Administrator’s
the
judgment on the adequacy of the current the literature has expanded since
completion of the 2019 ISA.51 The 2019
primary PM2.5 standards. As such, the
ISA evaluated a couple of controlled
ISA Supplement builds on the
human exposure studies that
information presented within the 2019
investigated the effect of exposure to
ISA with a targeted identification and
evaluation of new scientific information near-ambient concentrations of PM2.5
(U.S. EPA, 2022a, section 1.2). The ISA
50 As noted in the ISA Supplement (U.S. EPA,
Supplement focuses on PM2.5 health
2022a, p. 1–3): ‘‘In the peer-reviewed literature,
effects evidence where the 2019 ISA
these epidemiologic studies are often referred to as
concludes a ‘‘causal relationship,’’
causal inference studies or studies that used causal
because such health effects are given the modeling methods. For the purposes of this
Supplement, this terminology is not used to prevent
most weight in an Administrator’s
confusion with the main scientific conclusions (i.e.,
decisions in a NAAQS review. As such, the causality determinations) presented within an
the ISA Supplement evaluates newly
ISA. In addition, as is consistent with the weightof-evidence framework used within ISAs and
available evidence related to short- and
long-term PM2.5 exposure and mortality discussed in the Preamble to the Integrated Science
Assessments, an individual study on its own cannot
and cardiovascular effects given the
inform causality, but instead represents a piece of
strength of the evidence available in the the overall body of evidence.’’
51 As with the epidemiologic studies for long- and
2019 ISA and past ISAs and AQCDs, as
short-term PM2.5 exposure and mortality and
well as the clear adversity of these
cardiovascular effects, epidemiologic studies of
endpoints. Specifically, U.S. and
exposure or risk disparities and SARS–CoV–2
Canadian epidemiologic studies for
infection and/or COVID–19 death were limited to
those conducted in the U.S. and Canada.
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pertaining to the public health risk of
PM in ambient air. In considering the
scientific and technical information
here, we consider both the information
available at the time of the 2020 review
and information more recently
available, including that which has been
critically analyzed and characterized in
the 2019 ISA and ISA Supplement. The
quantitative risk analyses, including a
newly conducted at-risk analysis,
provide a context for interpreting the
evidence of mortality and the potential
public health significance of risks
associated with air quality conditions
that just meet the current and potential
alternative standards. The overarching
purpose of these analyses is to inform
the Administrator’s conclusions on the
public health protection afforded by the
current primary standards, with an
important focus on evaluating the
potential for exposures and risks beyond
those indicated by the information
available at the time the current
standards were established.
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(U.S. EPA, 2019a, section 6.1.10 and
6.1.13). The ISA Supplement adds to
this limited evidence, including a recent
study conducted in young healthy
individuals exposed to near-ambient
PM2.5 concentrations (U.S. EPA, 2022a,
section 3.3.1). Given the importance of
identifying populations at increased risk
of PM2.5-related effects, the ISA
Supplement also included
epidemiologic or exposure studies that
examined whether there is evidence of
exposure or risk disparities by race/
ethnicity or SES. These types of studies
provide additional information related
to factors that may increase risk of
PM2.5-related health effects and provide
additional evidence for consideration by
the Administrator in reaching
conclusions regarding the adequacy of
the current standards. In addition, the
ISA Supplement evaluated studies that
examined the relationship between
short- and long-term PM2.5 exposures
and SARS–CoV–2 infection and/or
COVID–19 death, as these studies are a
new area of research and were raised by
a number of public commenters in the
2020 review.
The evidence presented within the
2019 ISA, along with the targeted
identification and evaluation of new
scientific information in the ISA
Supplement, provides the scientific
basis for the reconsideration of the 2020
final decision on the primary PM2.5
standards. The subsections below
briefly summarize the nature of PM2.5related health effects, with a focus on
those health effects for which the 2019
ISA concluded a ‘‘causal’’ or ‘‘likely to
be causal’’ relationship.
1. Nature of Effects
The evidence base available in the
reconsideration includes decades of
research on PM2.5-related health effects
(U.S. EPA, 2004b; U.S. EPA, 2009b; U.S.
EPA, 2019a), including the full body of
evidence evaluated in the 2019 ISA
(U.S. EPA, 2019a), along with the
targeted evaluation of recent evidence in
the ISA Supplement (U.S. EPA, 2022a).
In considering the available scientific
evidence, the sections below summarize
the relationships between long- and
short-term PM2.5 exposures and
mortality (II.B.1.a), cardiovascular
effects (II.B.1.b), respiratory effects
(II.B.1.c), cancer (II.B.1.d), and nervous
system effects (II.B.1.e). For these
outcomes, the 2019 ISA concluded that
the evidence supports either a ‘‘causal’’
or a ‘‘likely to be causal’’ relationship.52
52 In this reconsideration of the PM NAAQS, the
EPA considers the full body of health evidence,
placing the greatest emphasis on the health effects
for which the evidence has been judged in the 2019
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a. Mortality
i. Long-Term PM2.5 Exposures
In the 2012 review, the 2009 ISA
reported that the evidence was
‘‘sufficient to conclude that the
relationship between long-term PM2.5
exposures and mortality is causal’’ (U.S.
EPA, 2009a, p. 7–96). The strongest
evidence supporting this conclusion
was provided by epidemiologic studies,
particularly those examining two
seminal cohorts, the American Cancer
Society (ACS) cohort and the Harvard
Six Cities cohort. Analyses of the
Harvard Six Cities cohort included
evidence indicating that reductions in
ambient PM2.5 concentrations are
associated with reduced mortality risk
(Laden et al., 2006) and increases in life
expectancy (Pope et al., 2009). Further
support was provided by other cohort
studies conducted in North America
and Europe that reported positive
associations between long-term PM2.5
exposure and mortality (U.S. EPA,
2019a).
Cohort studies, which have become
available since the completion of the
2009 ISA and evaluated in the 2019 ISA,
continue to provide consistent evidence
of positive associations between longterm PM2.5 exposures and mortality.
These studies add support for
associations with all-cause and total
(non-accidental) mortality,53 as well as
with specific causes of mortality,
including cardiovascular disease and
respiratory disease (U.S. EPA, 2019a,
section 11.2.2). Several of these studies
conducted analyses over longer study
durations and periods of follow-up than
examined in the original ACS and
Harvard Six Cities cohort studies and
continue to report positive associations
between long-term exposure to PM2.5
and mortality (U.S. EPA, 2019a, section
11.2.2.1; Figures 11–18 and 11–19). In
addition to studies focusing on the ACS
and Harvard Six Cities cohorts,
additional studies examining other
cohorts also provide evidence of
consistent, positive associations
between long-term PM2.5 exposure and
mortality across a wide range of
demographic groups (e.g., age, sex,
occupation), spatial and temporal
extents, exposure assessment metrics,
and statistical techniques (U.S. EPA,
2019a, sections 11.2.2.1, 11.2.5; U.S.
EPA, 2022a, Table 11–8). This includes
some of the largest cohort studies
conducted to date, such as analyses of
ISA to demonstrate a ‘‘causal’’ or ‘‘likely to be
causal’’ relationship with PM2.5 exposures.
53 The majority of these studies examined nonaccidental mortality outcomes, though some
Medicare studies lack cause-specific death
information and, therefore, examine total mortality.
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the U.S. Medicare cohort that includes
nearly 61 million enrollees and studies
that control for a range of individual
and ecological covariates, including
race, age, SES, smoking status, body
mass index, and annual weather
variables (e.g., temperature, humidity)
(U.S. EPA, 2019a).
In addition to those cohort studies
evaluated in the 2019 ISA, recent North
American cohort studies evaluated in
the ISA Supplement continue to
examine the relationship between longterm PM2.5 exposure and mortality and
report consistent, positive and
statistically significant associations.
These recent studies also utilize large
and demographically diverse cohorts
that are generally representative of the
national populations in both the U.S.
and Canada. These ‘‘studies published
since the 2019 ISA support and extend
the evidence base that contributed to the
conclusion of a causal relationship
between long-term PM2.5 exposure and
mortality’’ (U.S. EPA, 2022a, section
3.2.2.2.1, Figure 3–19, Figure 3–20).
Furthermore, studies evaluated in the
2019 ISA and the ISA Supplement that
examined cause-specific mortality
expand upon previous research that
found consistent, positive associations
between PM2.5 exposure and specific
mortality outcomes, which include
cardiovascular and respiratory
mortality, as well as other mortality
outcomes. For cardiovascular-related
mortality, the evidence evaluated in the
ISA Supplement is consistent with the
evidence evaluated in the 2019 ISA with
recent studies reporting positive
associations with long-term PM2.5
exposure. When evaluating causespecific cardiovascular mortality, recent
studies reported positive associations
for a number of outcomes, such as
ischemic heart disease (IHD) and stroke
mortality (U.S. EPA, 2022a, Figure 3–
23). Moreover, recent studies also
provide some initial evidence that
individuals with pre-existing health
conditions, such as heart failure and
diabetes, are at an increased risk of
PM2.5-related health effects (U.S. EPA,
2022a, section 3.2.2.4) and that these
individuals have a higher risk of
mortality overall, which was previously
only examined in studies that used
stratified analyses rather than a cohort
of people with an underlying health
condition (U.S. EPA, 2022a, section
3.2.2.4). With regard to respiratory
mortality, epidemiologic studies
evaluated in the 2019 ISA and ISA
Supplement continue to provide
support for associations between longterm PM2.5 exposure and respiratory
mortality (U.S. EPA, 2019a, section
5.2.10; U.S. EPA, 2022a, Table 3–2).
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A series of epidemiologic studies
evaluated in the 2019 ISA tested the
hypothesis that past reductions in
ambient PM2.5 concentrations are
associated with increased life
expectancy or a decreased mortality rate
(U.S. EPA, 2022a, section 11.2.2.5).
Pope et al. (2009) conducted a crosssectional analysis using air quality data
from 51 metropolitan areas across the
U.S., beginning in the 1970s through the
early 2000s, and found that a 10 mg/m3
decrease in long-term PM2.5
concentration was associated with a
0.61-year increase in life expectancy. In
a subsequent analysis, the authors
extended the period of analysis to
include 2000 to 2007, a time period
with lower ambient PM2.5
concentrations (Correia et al., 2013). In
this follow-up study, a decrease in longterm PM2.5 concentration continued to
be associated with an increase in life
expectancy, though the magnitude of
the increase was smaller than during the
earlier time period (i.e., a 10 mg/m3
decrease in long-term PM2.5
concentration was associated with a
0.35-year increase in life expectancy).
Additional studies conducted in the
U.S. or Europe similarly report that
reductions in ambient PM2.5 are
associated with improvements in
longevity (U.S. EPA, 2022a, section
11.2.2.5). Since the literature cutoff date
for the 2019 ISA, a few epidemiologic
studies were published that examined
the relationship between long-term
PM2.5 exposure and life-expectancy
(U.S. EPA, 2022a, section 3.2.1.3) and
report results that are consistent with
and expand upon the body of evidence
from the 2019 ISA. For example,
reported that PM2.5 concentrations
above the lowest observed concentration
(2.8 mg/m3) were associated with a 0.15
year decrease in national life expectancy
for women and 0.13 year decrease in
national life expectancy for men (U.S.
EPA, 2022a, section 3.2.2.2.4, Figure 3–
25). Another study compared
participants living in areas with PM2.5
concentrations >12 mg/m3 to
participants living in areas with PM2.5
concentrations <12 mg/m3 and reported
that the number of years of life lost due
to living in areas with higher PM2.5
concentrations was 0.84 years over a 5year period (Ward-Caviness et al., 2020;
U.S. EPA, 2022a, section 3.2.2.2.4).
Additionally, a number of
accountability studies, which are
epidemiologic studies that evaluate
whether an environmental policy or air
quality intervention resulted in
reductions in ambient air pollution
concentrations and subsequent
reductions in mortality, have emerged
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and were evaluated in the ISA
Supplement (U.S. EPA, 2022a, section
3.2.2.3). For example, Sanders et al.
(2020a) examined whether policy
actions (i.e., the first annual PM2.5
NAAQS implementation rule in 2005
for the 1997 annual PM2.5 standard with
a 3-year annual average of 15.0 mg/m3)
reduced PM2.5 concentrations and
mortality rates in Medicare beneficiaries
between 2000–2013, and found that
following implementation of the annual
PM2.5 NAAQS, annual PM2.5
concentrations decreased by 1.59 mg/m3
(95% CI: 1.39, 1.80) which
corresponded to a reduction in mortality
rates among individuals 65 years and
older (0.93% [95% CI: 0.10%, 1.77%])
in non-attainment counties relative to
attainment counties.
The 2019 ISA also evaluated a small
number of studies that used alternative
methods for confounder control to
further assess relationship between
long-term PM2.5 exposure and mortality
(U.S. EPA, 2019a, section 11.2.2.4). In
addition, multiple epidemiologic
studies that implemented alternative
methods for confounder control and
were published since the literature
cutoff date of the 2019 ISA were
evaluated in the ISA Supplement (U.S.
EPA, 2022a, section 3.2.2.3). These
studies used a variety of statistical
methods including generalized
propensity score (GPS), inverse
probability weighting (IPW), and
difference-in-difference (DID) to reduce
uncertainties related to confounding
bias in the association between longterm PM2.5 exposure and mortality.
Studies that employed these alternative
methods for confounder control
reported consistent positive associations
between long-term PM2.5 exposure and
total mortality (U.S. EPA, 2022a, section
3.2.2.3), and provided further support
for the associations reported in the
cohort studies referenced above.
The 2019 ISA and ISA Supplement
also evaluated the degree to which
recent studies examining the
relationship between long-term PM2.5
exposure and mortality addressed key
policy-relevant issues and/or previously
identified data gaps in the scientific
evidence, including methods to estimate
exposure, methods to control for
confounding (e.g., co-pollutant
confounding), the shape of the C–R
relationship, as well as examining
whether a threshold exists below which
mortality effects do not occur. For
example, with respect to exposure
assessment, based on its evaluation of
the evidence, the 2019 ISA concludes
that positive associations between longterm PM2.5 exposures and mortality are
robust across recent analyses using
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various approaches to estimate PM2.5
exposures (e.g., based on monitors,
models, satellite-based methods, or
hybrid methods that combine
information from multiple sources)
(U.S. EPA, 2019a, section 11.2.5.1). Hart
et al. (2015) report that correction for
bias due to exposure measurement error
increases the magnitude of the hazard
ratios (confidence intervals widen but
the association remains statistically
significant), suggesting that failure to
correct for exposure measurement error
could result in attenuation or
underestimation of risk estimates.
The 2019 ISA additionally concludes
that positive associations between longterm PM2.5 exposures and mortality are
robust across statistical models that use
different approaches to control for
confounders or different sets of
confounders (U.S. EPA, 2019a, sections
11.2.3 and 11.2.5), across diverse
geographic regions and populations, and
across a range of temporal periods
including periods of declining PM
concentrations (U.S. EPA, 2019a,
sections 11.2.2.5 and 11.2.5.3).
Additional evidence further
demonstrates that associations with
mortality remain robust in copollutants
analyses (U.S. EPA, 2019a, section
11.2.3), and that associations persist in
analyses restricted to long-term
exposures (annual average PM2.5
concentrations) below 12 mg/m3 (Di et
al., 2017b) or 10 mg/m3 (Shi et al., 2016),
indicating that risks are not
disproportionately driven by the upper
portions of the air quality distribution.
Recent studies evaluated in the ISA
Supplement further assess potential
copollutant confounding and indicate
that while there is some evidence of
potential confounding of the PM2.5mortality association by copollutants in
some of the studies (i.e., those studies of
the Mortality Air Pollution Associations
in Low Exposure Environments
(MAPLE) cohort), this result is
inconsistent with other recent studies
evaluated in the 2019 ISA that were
conducted in the U.S. and Canada that
found associations in both single and
copollutant models (U.S. EPA, 2019a;
U.S. EPA, 2022a, section 3.2.2.4)
Additionally, a few studies use
statistical techniques to reduce
uncertainties related to potential
confounding to further inform
conclusions on causality for long-term
PM2.5 exposure and mortality. For
example, studies by Greven et al. (2011),
Pun et al. (2017), and Eum et al. (2018)
completed sensitivity analyses as part of
their Medicare cohort study in which
they decompose ambient PM2.5 into
‘‘spatial’’ and ‘‘spatiotemporal’’
components in order to evaluate the
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potential for bias due to unmeasured
spatial confounding. Pun et al. (2017)
observed positive associations for the
‘‘temporal’’ variation model and
approximately null associations for the
‘‘spatiotemporal’’ variation model for all
causes of death except for chronic
obstructive pulmonary disease (COPD)
mortality. The difference in the results
of these two models for most causes of
death suggests the presence of
unmeasured confounding, though the
authors do not indicate anything about
the direction or magnitude of this bias.
It is important to note that the
‘‘temporal’’ and ‘‘spatiotemporal’’
coefficients are not directly comparable
to the results of other epidemiologic
studies when examined individually
and can only be used in comparison
with one another to evaluate the
potential for unmeasured confounding
bias. Eum et al. (2018) and Wu et al.
(2020) also attempted to address longterm trends and meteorological
variables as potential confounders and
found that not adjusting for temporal
trends could overestimate the
association, while effect estimates in
analyses that excluded meteorological
variables remained unchanged
compared to the main analyses. While
results of these analyses suggest the
presence of some unmeasured
confounding, they do not indicate the
direction or magnitude of the bias.54
An additional important
consideration in characterizing the
public health impacts associated with
PM2.5 exposure is whether C–R
relationships are linear across the range
of concentrations or if nonlinear
relationships exist along any part of this
range. Studies evaluated in the 2019 ISA
and the ISA Supplement examine this
issue, and continue to provide evidence
of linear, no-threshold relationships
between long-term PM2.5 exposures and
all-cause and cause-specific mortality
(U.S. EPA, 2019a, section 11.2.4; U.S.
EPA, 2022a, section 3.2.2.2.7, Table 3–
6). Across the studies evaluated in the
2019 ISA and the ISA Supplement, a
variety of statistical methods have been
used to assess whether there is evidence
of deviations in linearity (U.S. EPA,
2019a, Table 11–7; U.S. EPA, 2022a,
section 2.2.3.2). Studies have also
54 In public comments on the 2019 draft PA, the
authors of the Pun et al. (2017) study further note
that ‘‘the presence of unmeasured confounding . . .
was expected given that we did not control for
several potential confounders that may impact
PM2.5-mortality associations, such as smoking,
socio-economic status (SES), gaseous pollutants,
PM2.5 components, and long-term time trends in
PM2.5’’ and that ‘‘spatial confounding may bias
mortality risks both towards and away from the
null’’ (Docket ID EPA–HQ–OAR–2015–0072–0065;
accessible in https://www.regulations.gov/).
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conducted cut-point analyses that focus
on examining risk at specific ambient
PM2.5 concentrations. Generally, the
evidence remains consistent in
supporting a no-threshold relationship,
and in supporting a linear relationship
for PM2.5 concentrations > 8 mg/m3.
However, uncertainties remain about
the shape of the C–R curve at PM2.5
concentrations < 8 mg/m3, with some
recent studies providing evidence for
either a sublinear, linear, or supralinear
relationship at these lower
concentrations (U.S. EPA, 2019a,
section 11.2.4; U.S. EPA, 2022a, section
2.2.3.2). There was also some limited
evidence indicating that the slope of the
C–R function may be steeper
(supralinear) at lower concentrations for
cardiovascular mortality (U.S. EPA,
2022a, section 3.1.1.2.6).
The biological plausibility of PM2.5attributable mortality is supported by
the coherence of effects across scientific
disciplines (i.e., animal toxicological,
controlled human exposure studies, and
epidemiologic) when evaluating
respiratory and cardiovascular
morbidity effects, which are some of the
largest contributors to total
(nonaccidental) mortality. The 2019 ISA
outlines the available evidence for
biologically plausible pathways by
which inhalation exposure to PM2.5
could progress from initial events (e.g.,
pulmonary inflammation, autonomic
nervous system activation) to endpoints
relevant to population outcomes,
particularly those related to
cardiovascular diseases such as
ischemic heart disease, stroke and
atherosclerosis (U.S. EPA, 2019a,
section 6.2.1), and to metabolic effects,
including diabetes (U.S. EPA, 2019a,
section 7.3.1). The 2019 ISA notes
‘‘more limited evidence from respiratory
morbidity’’ (U.S. EPA, 2019a, p. 11–101)
such as development of chronic
obstructive pulmonary disease (COPD)
(U.S. EPA, 2019a, section 5.2.1) to
support the biological plausibility of
mortality due to long-term PM2.5
exposures (U.S. EPA, 2019a, section
11.2.1).
Taken together, epidemiologic studies
evaluated in the 2019 ISA, including
recent studies evaluated in the ISA
Supplement, consistently report
positive associations between long-term
PM2.5 exposure and mortality across
different geographic locations,
populations, and analytic approaches
(U.S. EPA, 2019a; U.S. EPA, 2022a,
section 3.2.2.4). As such, these studies
reduce key uncertainties identified in
previous reviews, including those
related to potential copollutant
confounding, and provide additional
information on the shape of the C–R
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curve. As evaluated in the 2019 ISA,
experimental and epidemiologic
evidence for cardiovascular effects, and
respiratory effects to a more limited
degree, supports the plausibility of
mortality due to long-term PM2.5
exposures. Overall, studies evaluated in
the 2019 ISA support the conclusion of
a causal relationship between long-term
PM2.5 exposure and mortality, which is
supported and extended by evidence
from recent epidemiologic studies
evaluated in the ISA Supplement (U.S.
EPA, 2022a, section 3.2.2.4).
ii. Short-Term PM2.5 Exposures
The 2009 ISA concluded that ‘‘a
causal relationship exists between shortterm exposure to PM2.5 and mortality’’
(U.S. EPA, 2009a). This conclusion was
based on the evaluation of both multiand single-city epidemiologic studies
that consistently reported positive
associations between short-term PM2.5
exposure and non-accidental mortality.
These associations were strongest, in
terms of magnitude and precision,
primarily at lags of 0 to 1 days.
Examination of the potential
confounding effects of gaseous
copollutants was limited, though
evidence from single-city studies
indicated that gaseous copollutants have
minimal effect on the PM2.5-mortality
relationship (i.e., associations remain
robust to inclusion of other pollutants in
copollutant models). The evaluation of
cause-specific mortality found that
effect estimates were larger in
magnitude, but also had larger
confidence intervals, for respiratory
mortality compared to cardiovascular
mortality. Although the largest mortality
risk estimates were for respiratory
mortality, the interpretation of the
results was complicated by the limited
coherence from studies of respiratory
morbidity. However, the evidence from
studies of cardiovascular morbidity
provided both coherence and biological
plausibility for the relationship between
short-term PM2.5 exposure and
cardiovascular mortality.
Multicity studies evaluated in the
2019 ISA and the ISA Supplement
provide evidence of primarily positive
associations between daily PM2.5
exposures and mortality, with percent
increases in total mortality ranging from
0.19% (Lippmann et al., 2013) to 2.80%
(Kloog et al.) 55 at lags of 0 to 1 days in
single-pollutant models. Whereas many
studies assign exposures using data
from ambient monitors, other studies
55 As detailed in the Preface to the ISA, risk
estimates are for a 10 mg/m3 increase in 24-hour avg
PM2.5 concentrations, unless otherwise noted (U.S.
EPA, 2019a).
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employ hybrid modeling approaches,
which estimate PM2.5 concentrations
using data from a variety of sources (i.e.,
from satellites, land use information,
and modeling, in addition to monitors)
and enable the inclusion of less urban
and more rural locations in analyses
(Kloog et al., 2013, Lee et al., 2015, Shi
et al., 2016).
Some studies have expanded the
examination of potential confounders
including long-term temporal trends,
weather, and co-occurring pollutants.
Mortality associations were found to
remain positive, although in some cases
were attenuated, when using different
approaches to account for temporal
trends or weather covariates (e.g., U.S.
EPA, 2019a, section 11.1.5.1). For
example, Sacks et al. (2012) examined
the influence of model specification
using the approaches for confounder
adjustment from models employed in
several multicity studies within the
context of a common data set (U.S. EPA,
2019a, section 11.1.5.1). These models
use different approaches to control for
long-term temporal trends and the
potential confounding effects of
weather. The authors report that
associations between daily PM2.5 and
cardiovascular mortality were similar
across models, with the percent increase
in mortality ranging from 1.5–2.0%
(U.S. EPA, 2019a, Figure 11–4). Thus,
alternative approaches to controlling for
long-term temporal trends and for the
potential confounding effects of weather
may influence the magnitude of the
association between PM2.5 exposures
and mortality but have not been found
to influence the direction of the
observed association (U.S. EPA, 2019a,
section 11.1.5.1). Taken together, the
2019 ISA and the ISA Supplement
conclude that recent multicity studies
conducted in the U.S., Canada, Europe,
and Asia continue to provide consistent
evidence of positive associations
between short-term PM2.5 exposures and
total mortality across studies that use
different approaches to control for the
potential confounding effects of weather
(e.g., temperature) (U.S. EPA, 2019a,
section 1.4.1.5.1; U.S. EPA, 2022a,
section 3.2.1.2).
With regard to copollutants, studies
evaluated in the 2019 ISA provide
additional evidence that associations
between short-term PM2.5 exposures and
mortality remain positive and relatively
unchanged in copollutant models with
both gaseous pollutants and PM10–2.5
(U.S. EPA, 2019a, section 11.1.4).
Additionally, the low (r < 0.4) to
moderate correlations (r = 0.4–0.7)
between PM2.5 and gaseous pollutants
and PM10–2.5 increase the confidence in
PM2.5 having an independent effect on
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mortality (U.S. EPA, 2019a, section
11.1.4). Consistent with the studies
evaluated in the 2019 ISA, studies
evaluated in the ISA Supplement that
used data from more recent years also
indicate that associations between shortterm PM2.5 exposure and mortality
remain unchanged in copollutant
models. However, the evidence
indicates that the association could be
larger in magnitude in the presence of
some copollutants such as oxidant gases
(Lavigne et al., 2018; Shin et al., 2021).
The generally positive associations
reported with mortality are supported
by a small group of studies employing
alternative methods for confounder
control or quasi-experimental statistical
approaches (U.S. EPA, 2019a, section
11.1.2.1). For example, two studies by
Schwartz et al. report associations
between PM2.5 instrumental variables
and mortality (U.S. EPA, 2019a, Table
11–2), including in an analysis limited
to days with 24-hour average PM2.5
concentrations <30 mg/m3 (Schwartz et
al., 2015; Schwartz et al., 2017). In
addition to the main analyses, these
studies conducted Granger-like
causality tests as sensitivity analyses to
examine whether there was evidence of
an association between mortality and
PM2.5 after the day of death, which
would support the possibility that
unmeasured confounders were not
accounted for in the statistical model.
Neither study reports evidence of an
association with PM2.5 after death (i.e.,
they do not indicate unmeasured
confounding). Yorifuji et al. (2016)
conducted a quasi-experimental study
to examine whether a specific regulatory
action in Tokyo, Japan (i.e., a diesel
emission control ordinance), resulted in
a subsequent reduction in daily
mortality (Yorifuji et al., 2016). The
authors reported a reduction in
mortality in Tokyo due to the ordinance,
compared to Osaka, which did not have
a similar diesel emission control
ordinance in place. In another study,
Schwartz et al. (2018) utilized three
statistical methods including
instrumental variable analysis, a
negative exposure control, and marginal
structural models to estimate the
association between PM2.5 and daily
mortality (Schwartz et al., 2018). Results
from this study continue to support a
relationship between short-term PM2.5
exposure and mortality. Additional
epidemiologic studies evaluated in the
ISA Supplement that employed
alternative methods for confounder
control to examine the association
between short-term PM2.5 exposure and
mortality also report consistent positive
associations in studies that examine
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effects across multiple cities in the U.S.
(U.S. EPA, 2022a).
The positive associations for total
mortality reported across the majority of
studies evaluated are further supported
by analyses reporting generally
consistent, positive associations with
both cardiovascular and respiratory
mortality (U.S. EPA, 2019a, section
11.1.3). Recent multicity studies
evaluated in the ISA Supplement add to
the body of evidence indicating a
relationship between short-term PM2.5
exposure and cause-specific mortality,
with more variability in the magnitude
and precision of associations for
respiratory mortality (U.S. EPA, 2022a;
Figure 3–14. For both cardiovascular
and respiratory mortality, there has been
a limited assessment of potential
copollutant confounding, though initial
evidence indicates that associations
remain positive and relatively
unchanged in models with gaseous
pollutants and PM10–2.5. This evidence
further supports the copollutant
analyses conducted for total mortality.
The strong evidence for ischemic events
and heart failure, as detailed in the
assessment of cardiovascular morbidity
(U.S. EPA, 2019a, Chapter 6), provides
biological plausibility for PM2.5-related
cardiovascular mortality, which
comprises the largest percentage of total
mortality (i.e., ∼33%) (National Heart,
Lung, and Blood Institute (NHLBI),
2017). Although there is evidence for
exacerbations of COPD and asthma, the
collective body of respiratory morbidity
evidence provides limited biological
plausibility for PM2.5-related respiratory
mortality (U.S. EPA, 2019a, Chapter 5).
In the 2009 ISA, one of the main
uncertainties identified was the regional
and city-to-city heterogeneity in PM2.5mortality associations. Studies
evaluated in the 2019 ISA examine both
city-specific as well as regional
characteristics to identify the
underlying contextual factors that could
contribute to this heterogeneity (U.S.
EPA, 2019a, section 11.1.6.3). Analyses
focusing on effect modification of the
PM2.5 mortality relationship by PM2.5
components, regional patterns in PM2.5
components and city specific
differences in composition and sources
indicate some differences in the PM2.5
composition and sources across cities
and regions, but these differences do not
fully explain the observed
heterogeneity. Additional studies find
that factors related to potential exposure
differences, such as housing stock and
commuting, as well as city specific
factors (e.g., land use, port volume, and
traffic information), may also explain
some of the observed heterogeneity
(U.S. EPA, 2019a, section 11.1.6.3).
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Collectively, studies evaluated in the
2019 ISA and the ISA Supplement
indicate that the heterogeneity in PM2.5
mortality risk estimates cannot be
attributed to one factor, but instead a
combination of factors including, but
not limited to, PM composition and
sources as well as community
characteristics that could influence
exposures (U.S. EPA, 2019a, section
11.1.12; U.S. EPA, 2022a, section
3.2.1.2.1).
A number of studies conducted
systematic evaluations of the lag
structure of associations for the PM2.5mortality relationship by examining
either a series of single day or multiday
lags and these studies continue to
support an immediate effect (i.e., lag 0
to 1 days) of short-term PM2.5 exposures
on mortality (U.S. EPA, 2019a, section
11.1.8.1; U.S. EPA, 2022a, section
3.2.1.1). Recent studies also conducted
analyses comparing the traditional 24hour average exposure metric with a
sub-daily metric (i.e., 1-hour max).
These initial studies provide evidence
of a similar pattern of associations for
both the 24-hour average and 1-hour
max metric, with the association larger
in magnitude for the 24-hour average
metric.
Multicity studies indicate that
positive and statistically significant
associations with mortality persist in
analyses restricted to short-term (24hour average PM2.5 concentrations)
PM2.5 exposures below 35 mg/m3 (Lee et
al., 2015),56 below 30 mg/m3 (Shi et al.,
2016), and below 25 mg/m3 (Di et al.,
2017a), indicating that risks associated
with short-term PM2.5 exposures are not
disproportionately driven by the peaks
of the air quality distribution.
Additional studies examined the shape
of the C–R relationship for short-term
PM2.5 exposure and mortality and
whether a threshold exists below which
mortality effects do not occur (U.S. EPA,
2019a, section 11.1.10). These studies
used various statistical approaches and
consistently demonstrate linear C–R
relationships with no evidence of a
threshold. Moreover, recent studies
evaluated in the ISA Supplement
provide additional support for a linear,
no-threshold C–R relationship between
short-term PM2.5 exposure and
mortality, with confidence in the shape
decreasing at concentrations below 5 mg/
m3 (Shi et al., 2016; Lavigne et al.,
2018). Recent analyses provide initial
evidence indicating that PM2.5-mortality
associations persist and may be stronger
56 Lee et al. (2015) also report that positive and
statistically significant associations between shortterm PM2.5 exposures and mortality persist in
analyses restricted to areas with long-term
concentrations below 12 mg/m3.
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(i.e., a steeper slope) at lower
concentrations (e.g., Di et al., 2017a;
Figure 11–12 in U.S. EPA, 2019).
However, given the limited data
available at the lower end of the
distribution of ambient PM2.5
concentrations, the shape of the C–R
curve remains uncertain at these low
concentrations. Although difficulties
remain in assessing the shape of the
short-term PM2.5-mortality C–R
relationship, to date, studies have not
conducted systematic evaluations of
alternatives to linearity and recent
studies evaluated in the ISA
Supplement continue to provide
evidence of a no-threshold linear
relationship, with less confidence at
concentrations lower than 5 mg/m3.
Overall, epidemiologic studies
evaluated in the 2019 ISA and the ISA
Supplement build upon and extend the
conclusions of the 2009 ISA for the
relationship between short-term PM2.5
exposures and total mortality.
Supporting evidence for PM2.5-related
cardiovascular morbidity, and more
limited evidence from respiratory
morbidity, provide biological
plausibility for mortality due to shortterm PM2.5 exposures. The primarily
positive associations observed across
studies conducted in diverse geographic
locations is further supported by the
results from copollutant analyses
indicating robust associations, along
with evidence from analyses examining
the C–R relationship. Overall, studies
evaluated in the 2019 ISA support the
conclusion of a causal relationship
between short-term PM2.5 exposure and
mortality, which is supported by
evidence from recent epidemiologic
studies evaluated in the ISA
Supplement (U.S. EPA, 2022a, section
3.2.1.4, p. 3–69).
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b. Cardiovascular Effects
i. Long-Term PM2.5 Exposures
The scientific evidence reviewed in
the 2009 ISA was ‘‘sufficient to infer a
causal relationship between long-term
PM2.5 exposure and cardiovascular
effects’’ (U.S. EPA, 2009a). The strongest
line of evidence comprised findings
from several large epidemiologic studies
of U.S. and Canadian cohorts that
reported consistent positive associations
between long-term PM2.5 exposure and
cardiovascular mortality (Pope et al.,
2004; Krewski et al., 2009; Miller et al.,
2007; Laden et al., 2006). Studies of
long-term PM2.5 exposure and
cardiovascular morbidity were limited
in number. Biological plausibility and
coherence with the epidemiologic
findings were provided by studies using
genetic mouse models of atherosclerosis
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demonstrating enhanced atherosclerotic
plaque development and inflammation,
as well as changes in measures of
impaired heart function, following 4- to
6-month exposures to PM2.5
concentrated ambient particles (CAPs),
and by a limited number of studies
reporting CAPs-induced effects on
coagulation factors, vascular reactivity,
and worsening of experimentally
induced hypertension in mice (U.S.
EPA, 2009b).
Consistent with the evidence assessed
in the 2009 ISA, the 2019 ISA concludes
that recent studies, together with the
evidence available in previous reviews,
support a causal relationship between
long-term exposure to PM2.5 and
cardiovascular effects. Additionally,
recent epidemiologic studies published
since the completion of the 2019 ISA
and evaluated in the ISA Supplement
expands the body of evidence and
further supports such a conclusion (U.S.
EPA, 2022a). As discussed above
(section II.B.1.a), results from U.S. and
Canadian cohort studies evaluated in
the 2019 ISA conducted at varying
spatial and temporal scales and
employing a variety of exposure
assessment and statistical methods
consistently report positive associations
between long-term PM2.5 exposure and
cardiovascular mortality (U.S. EPA,
2019, Figure 6–19, section 6.2.10).
Positive associations between long-term
PM2.5 exposures and cardiovascular
mortality are generally robust in
copollutant models adjusted for ozone,
NO2, PM10–2.5, or SO2. In addition, most
of the results from analyses examining
the shape of the C–R relationship
between long-term PM2.5 exposures and
cardiovascular mortality support a
linear relationship and do not identify
a threshold below which mortality
effects do not occur (U.S. EPA, 2019a,
section 6.2.16, Table 6–52).
The body of literature examining the
relationship between long-term PM2.5
exposure and cardiovascular morbidity
has greatly expanded since the 2009
ISA, with positive associations reported
in several cohorts evaluated in the 2019
ISA (U.S. EPA, 2019a, section 6.2).
Though results for cardiovascular
morbidity are less consistent than those
for cardiovascular mortality (U.S. EPA,
2019a, section 6.2), studies in the 2019
ISA and the ISA Supplement provide
some evidence for associations between
long-term PM2.5 exposures and the
progression of cardiovascular disease.
Positive associations with
cardiovascular morbidity (e.g., coronary
heart disease, stroke, arrhythmias,
myocardial infarction (MI),
atherosclerosis progression) are
observed in several epidemiologic
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studies (U.S. EPA, 2019a, sections 6.2.2
to 6.2.9; U.S. EPA, 2022a, section
3.1.2.2). Additionally, studies evaluated
in the ISA Supplement report positive
associations among those with preexisting conditions, among patients
followed after a cardiac event
procedure, and among those with a first
hospital admission for heart attacks
among older adults enrolled in
Medicare (U.S. EPA, 2022a, sections
3.1.1 and 3.1.2).
Recent studies published since the
literature cutoff date of the 2019 ISA
further assessed the relationship
between long-term PM2.5 exposure and
cardiovascular effects by conducting
accountability analyses or by using
alternative methods for confounder
control in evaluating the association
between long-term PM2.5 exposure and
cardiovascular hospital admissions
(U.S. EPA, 2022a, section 3.1.2.3).
Studies that apply alternative methods
for confounder control increase
confidence in the relationship between
long-term PM2.5 exposure and
cardiovascular effects by using methods
that reduce uncertainties related to
potential confounding through
statistical and/or study design
approaches. For example, to control for
potential confounding Wei et al. (2021)
used a doubly robust additive model
(DRAM) and found an association
between long-term exposure to PM2.5
and cardiovascular effects, including
MI, stoke, and atrial fibrillation, among
the Medicare population. Additionally,
an accountability study by Henneman et
al. (2019a) utilized a difference-indifference (DID) approach to determine
the relationship between coal-fueled
power plant emissions and
cardiovascular effects and found that
reductions in PM2.5 concentrations
resulted in reductions of cardiovascularrelated hospital admissions.
Furthermore, several recent
epidemiologic studies evaluated in the
ISA Supplement reported that the
association between long-term PM2.5
exposure with stroke persisted after
adjustment for NO2 but was attenuated
in the model with O3 and oxidant gases
represented by the redox weighted
average of NO2 and O3 (U.S. EPA, 2022a,
section 3.1.2.2.8). Overall, these studies
report consistent findings that long-term
PM2.5 exposure is related to increased
hospital admissions for a variety of
cardiovascular disease outcomes among
large nationally representative cohorts
and provide additional support for a
relationship between long-term PM2.5
exposure and cardiovascular effects.
The positive associations reported in
epidemiologic studies are supported by
toxicological evidence for increased
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plaque progression in mice following
long-term exposure to PM2.5 collected
from multiple locations across the U.S.
(U.S. EPA, 2019a, section 6.2.4.2). A
small number of epidemiologic studies
also report positive associations
between long-term PM2.5 exposure and
heart failure, changes in blood pressure,
and hypertension (U.S. EPA, 2019a,
sections 6.2.5 and 6.2.7). Associations
with heart failure are supported by
animal toxicological studies
demonstrating decreased cardiac
contractility and function, and
increased coronary artery wall thickness
following long-term PM2.5 exposure
(U.S. EPA, 2019a, section 6.2.5.2).
Similarly, a limited number of animal
toxicological studies demonstrating a
relationship between long-term PM2.5
exposure and consistent increases in
blood pressure in rats and mice are
coherent with epidemiologic studies
reporting positive associations between
long-term exposure to PM2.5 and
hypertension.
Moreover, a number of studies
evaluated in the ISA Supplement
focusing on morbidity outcomes,
including those that focused on
incidence of MI, atrial fibrillation (AF),
stroke, and congestive heart failure
(CHF), expand the evidence pertaining
to the shape of the C–R relationship
between long-term PM2.5 exposure and
cardiovascular effects. These studies use
statistical techniques that allow for
departures from linearity (U.S. EPA,
2022a, Table 3–3), and generally
support the evidence characterized in
the 2019 ISA showing linear, nothreshold C–R relationship for most
cardiovascular disease (CVD) outcomes.
However, there is evidence for a
sublinear or supralinear C–R
relationship for some outcomes (U.S.
EPA, 2022a, section 3.1.2.2.9).57
Longitudinal epidemiologic analyses
also report positive associations with
markers of systemic inflammation (U.S.
EPA, 2019a, section 6.2.11), coagulation
(U.S. EPA, 2019a, section 6.2.12), and
endothelial dysfunction (U.S. EPA,
2019a, section 6.2.13). These results are
coherent with animal toxicological
studies generally reporting increased
markers of systemic inflammation,
oxidative stress, and endothelial
dysfunction (U.S. EPA, 2019a, section
6.2.12.2 and 6.2.14).
The 2019 ISA concludes that there is
consistent evidence from multiple
epidemiologic studies illustrating that
long-term exposure to PM2.5 is
57 As noted above for mortality, uncertainty in the
shape of the C–R relationship increases near the
upper and lower ends of the distribution due to
limited data.
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associated with mortality from
cardiovascular causes. Epidemiologic
studies evaluated in the ISA
Supplement provide additional
evidence of positive associations
between long-term PM2.5 exposure and
cardiovascular morbidity (U.S. EPA,
2022a, section 3.1.2.2). Associations
with coronary heart disease (CHD),
stroke and atherosclerosis progression
were observed in several additional
epidemiologic studies providing
coherence with the mortality findings.
Results from copollutant models
generally support an independent effect
of PM2.5 exposure on mortality.
Additional evidence of the independent
effect of PM2.5 on the cardiovascular
system is provided by experimental
studies in animals, which support the
biological plausibility of pathways by
which long-term exposure to PM2.5
could potentially result in outcomes
such as CHD, stroke, CHF, and
cardiovascular mortality. Overall,
studies evaluated in the 2019 ISA
support the conclusion of a causal
relationship between long-term PM2.5
exposure and cardiovascular effects,
which is supported and extended by
evidence from recent epidemiologic
studies evaluated in the ISA
Supplement (U.S. EPA, 2022a, section
3.1.2.2).
ii. Short-Term PM2.5 Exposures
The 2009 ISA concluded that ‘‘a
causal relationship exists between shortterm exposure to PM2.5 and
cardiovascular effects’’ (U.S. EPA,
2009a). The strongest evidence in the
2009 ISA was from epidemiologic
studies of emergency department (ED)
visits and hospital admissions for IHD
and heart failure (HF), with supporting
evidence from epidemiologic studies of
cardiovascular mortality (U.S. EPA,
2009a). Animal toxicological studies
provided coherence and biological
plausibility for the positive associations
reported with MI, ED visits, and
hospital admissions. These included
studies reporting reduced myocardial
blood flow during ischemia and studies
indicating altered vascular reactivity. In
addition, effects of PM2.5 exposure on a
potential indicator of ischemia (i.e., ST
segment depression on an
electrocardiogram) were reported in
both animal toxicological and
epidemiologic panel studies.58 Key
uncertainties from the last review
resulted from inconsistent results across
58 Some animal studies included in the 2009 ISA
examined exposures to mixtures, such as motor
vehicle exhaust or woodsmoke. In these studies, it
was unclear if the resulting cardiovascular effects
could be attributed specifically to the fine particle
component of the mixture.
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disciplines with respect to the
relationship between short-term
exposure to PM2.5 and changes in blood
pressure, blood coagulation markers,
and markers of systemic inflammation.
In addition, while the 2009 ISA
identified a growing body of evidence
from controlled human exposure and
animal toxicological studies,
uncertainties remained with respect to
biological plausibility.
Studies evaluated in the 2019 ISA
provide additional support for a causal
relationship between short-term PM2.5
exposure and cardiovascular effects.
This includes generally positive
associations observed in multicity
epidemiologic studies of emergency
department visits and hospital
admissions for IHD, heart failure (HF),
and combined cardiovascular-related
endpoints. In particular, nationwide
studies of older adults (65 years and
older) using Medicare records report
positive associations between PM2.5
exposures and hospital admissions for
HF (U.S. EPA, 2019a, section 6.1.3.1).
Moreover, recent multicity studies,
published after the literature cutoff date
of the 2019 ISA and evaluated in the
ISA Supplement, are consistent with
studies evaluated in the 2019 ISA that
report positive association between
short-term PM2.5 exposure and ED visits
and hospital admission for IHD, heart
attacks, and HF (U.S. EPA, 2022a,
section 3.1). Epidemiologic studies
conducted in single cities contribute
some support to the causality
determination, though associations
reported in single-city studies are less
consistently positive than in multicity
studies, and include a number of studies
reporting null associations (U.S. EPA,
2019a, sections 6.1.2 and 6.1.3). When
considered as a whole; however, the
recent body of IHD and HF
epidemiologic evidence supports the
evidence from previous ISAs reporting
mainly positive associations between
short-term PM2.5 concentrations and
emergency department visits and
hospital admissions.
The ISA Supplement also includes
some epidemiologic studies, published
since the literature cutoff date for the
2019 ISA, including accountability
analyses and epidemiologic studies that
employ alternative methods for
confounder control to evaluate the
association between short-term PM2.5
exposure and cardiovascular-related
effects (U.S. EPA, 2022a, section
3.1.1.3). These studies report positive
associations across a number of
statistical approaches, providing
additional support for a relationship
between short-term PM2.5 exposure and
cardiovascular effects, while also
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reducing uncertainties related to
potential confounder bias.
Consistent with the evidence assessed
in the 2019 ISA, some studies evaluated
in the ISA Supplement report no
evidence of an association with stroke,
regardless of stroke subtype.
Additionally, as in the 2019 ISA,
evidence evaluated in the ISA
Supplement continues to indicate an
immediate effect of PM2.5 on
cardiovascular-related outcomes
primarily within the first few days after
exposure, and that associations
generally persisted in models adjusted
for copollutants (U.S. EPA, 2022a,
section 3.1.1.2).
A number of controlled human
exposure, animal toxicological, and
epidemiologic panel studies provide
evidence that PM2.5 exposure could
plausibly result in IHD or HF through
pathways that include endothelial
dysfunction, arterial thrombosis, and
arrhythmia (U.S. EPA, 2019a, section
6.1.1). The most consistent evidence
from recent controlled human exposure
studies is for endothelial dysfunction, as
measured by changes in brachial artery
diameter or flow mediated dilation.
Multiple controlled human exposure
studies that examined the potential for
endothelial dysfunction report an effect
of PM2.5 exposure on measures of blood
flow (U.S. EPA, 2019a, section 6.1.13.2).
However, these studies report variable
results regarding the timing of the effect
and the mechanism by which reduced
blood flow occurs (i.e., availability vs
sensitivity to nitric oxide). In addition,
some controlled human exposure
studies using CAPs report evidence for
small increases in blood pressure (U.S.
EPA, 2019a, section 6.1.6.3). Although
not entirely consistent, there is also
some evidence across controlled human
exposure studies for conduction
abnormalities/arrhythmia (U.S. EPA,
2019a, section 6.1.4.3), changes in heart
rate variability (HRV) (U.S. EPA, 2019a,
section 6.1.10.2), changes in hemostasis
that could promote clot formation (U.S.
EPA, 2019a, section 6.1.12.2), and
increases in inflammatory cells and
markers (U.S. EPA, 2019a, section
6.1.11.2). A recent study by Wyatt et al.
(2020), evaluated in the ISA
Supplement, adds to the limited
evidence base of controlled human
exposure studies conducted at near
ambient PM2.5 concentrations. The
study, completed in healthy young
adults subject to intermittent exercise,
found some significant cardiovascular
effects (e.g., systematic inflammation
markers, including C-reactive protein
(CRP), and cardiac repolarization).
Thus, when taken as a whole, controlled
human exposure studies are coherent
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with epidemiologic studies in that they
demonstrate that short-term exposures
to PM2.5 may result in the types of
cardiovascular endpoints that could
lead to emergency department visits,
hospital admissions and mortality in
some people.
Animal toxicological studies
published since the 2009 ISA also
support a relationship between shortterm PM2.5 exposure and cardiovascular
effects. A study demonstrating
decreased cardiac contractility and left
ventricular pressure in mice is coherent
with the results of epidemiologic
studies that report associations between
short-term PM2.5 exposure and heart
failure (U.S. EPA, 2019a, section
6.1.3.3). In addition, and as with
controlled human exposure studies,
there is generally consistent evidence in
animal toxicological studies for
indicators of endothelial dysfunction
(U.S. EPA, 2019a, section 6.1.13.3).
Some studies in animals also provide
evidence for changes in a number of
other cardiovascular endpoints
following short-term PM2.5 exposure
including conduction abnormalities and
arrhythmia (U.S. EPA, 2019a, section
6.1.4.4), changes in HRV (U.S. EPA,
2019a, section 6.1.10.3), changes in
blood pressure (U.S. EPA, 2019a,
section 6.1.6.4), and evidence for
systemic inflammation and oxidative
stress (U.S. EPA, 2019a, section
6.1.11.3).
In summary, evidence evaluated in
the 2019 ISA extends the consistency
and coherence of the evidence base
evaluated in the 2009 ISA and prior
assessments. Direct evidence for an
independent effect of PM2.5 on
cardiovascular effects can be found in a
number of controlled human exposure
and animal toxicological studies, which
supports the results of epidemiologic
studies reporting that associations
remain relatively unchanged in
copollutant models. These results
concur with epidemiologic panel
studies reporting that PM2.5 exposure is
associated with some of the same
cardiovascular endpoints reported in
experimental studies. For some
cardiovascular effects, there are
inconsistencies in results across some
animal toxicological, controlled human
exposure, and epidemiologic panel
studies, though this may be due to
substantial differences in study design
and/or study populations. Overall, the
results from epidemiologic panel,
controlled human exposure, and animal
toxicological studies, in particular those
related to endothelial dysfunction,
impaired cardiac function, ST segment
depression, thrombosis, conduction
abnormalities, and changes in blood
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pressure provide coherence and
biological plausibility for the consistent
results from epidemiologic studies
observing positive associations between
short-term PM2.5 concentrations and
IHD and HF, and ultimately
cardiovascular mortality. Overall,
studies evaluated in the 2019 ISA
support the conclusion of a causal
relationship between short-term PM2.5
exposure and cardiovascular effects,
which is supported and extended by
evidence from recent epidemiologic
studies evaluated in the ISA
Supplement (U.S. EPA, 2022a, section
3.1.1.4).
c. Respiratory Effects
i. Long-Term PM2.5 Exposures
The 2009 ISA concluded that ‘‘a
causal relationship is likely to exist
between long-term PM2.5 exposure and
respiratory effects’’ (U.S. EPA, 2009a).
This conclusion was based mainly on
epidemiologic evidence demonstrating
associations between long-term PM2.5
exposure and changes in lung function
or lung function growth in children.
Biological plausibility was provided by
a single animal toxicological study
examining pre- and post-natal exposure
to PM2.5 CAPs, which found impaired
lung development. Epidemiologic
evidence for associations between longterm PM2.5 exposure and other
respiratory outcomes, such as the
development of asthma, allergic disease,
and COPD; respiratory infection; and
the severity of disease was limited, both
in the number of studies available and
the consistency of the results.
Experimental evidence for other
outcomes was also limited, with one
animal toxicological study reporting
that long-term exposure to PM2.5 CAPs
results in morphological changes in
nasal airways of healthy animals. Other
animal studies examined exposure to
mixtures, such as motor vehicle exhaust
and woodsmoke, and effects were not
attributed specifically to the particulate
components of the mixture.
Cohort studies evaluated in the 2019
ISA provided additional support for the
relationship between long-term PM2.5
exposure and decrements in lung
function growth (as a measure of lung
development), indicating a robust and
consistent association across study
locations, exposure assessment
methods, and time periods (U.S. EPA,
2019a, section 5.2.13). This relationship
was further supported by a retrospective
study that reports an association
between declining PM2.5 concentrations
and improvements in lung function
growth in children (U.S. EPA, 2019a,
section 5.2.11). Epidemiologic studies
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also examine asthma development in
children (U.S. EPA, 2019a, section
5.2.3), with prospective cohort studies
reporting generally positive
associations, though several are
imprecise (i.e., they report wide
confidence intervals). Supporting
evidence is provided by studies
reporting associations with asthma
prevalence in children, with childhood
wheeze, and with exhaled nitric oxide,
a marker of pulmonary inflammation
(U.S. EPA, 2019a, section 5.2.13).
Additionally, the 2019 ISA includes an
animal toxicological study showing the
development of an allergic phenotype
and an increase in a marker of airway
responsiveness supports the biological
plausibility of the development of
allergic asthma (U.S. EPA, 2019a,
section 5.2.13). Other epidemiologic
studies report a PM2.5-related
acceleration of lung function decline in
adults, while improvement in lung
function was observed with declining
PM2.5 concentrations (U.S. EPA, 2019a,
section 5.2.11). A longitudinal study
found declining PM2.5 concentrations
are also associated with an
improvement in chronic bronchitis
symptoms in children, strengthening
evidence reported in the 2009 ISA for a
relationship between increased chronic
bronchitis symptoms and long-term
PM2.5 exposure (U.S. EPA, 2019a,
section 5.2.11). A common uncertainty
across the epidemiologic evidence is the
lack of examination of copollutants to
assess the potential for confounding.
While there is some evidence that
associations remain robust in models
with gaseous pollutants, a number of
these studies examining copollutant
confounding were conducted in Asia,
and thus have limited generalizability
due to high annual pollutant
concentrations.
When taken together, the 2019 ISA
concludes that the ‘‘epidemiologic
evidence strongly supports a
relationship with decrements in lung
function growth in children’’ and ‘‘with
asthma development in children, with
increased bronchitis symptoms in
children with asthma, with an
acceleration of lung function decline in
adults, and with respiratory mortality
and cause-specific respiratory mortality
for COPD and respiratory infection’’
(U.S. EPA, 2019a, p. 1–34). In support
of the biological plausibility of such
associations reported in epidemiologic
studies of respiratory health effects,
animal toxicological studies continue to
provide direct evidence that long-term
exposure to PM2.5 results in a variety of
respiratory effects. Animal studies in
the 2019 ISA show pulmonary oxidative
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stress, inflammation, and morphologic
changes in the upper (nasal) and lower
airways. Other results show that
changes are consistent with the
development of allergy and asthma, and
with impaired lung development.
Overall, the 2019 ISA concludes that
‘‘the collective evidence is sufficient to
conclude that a causal relationship is
likely to exist between long-term PM2.5
exposure and respiratory effects’’ (U.S.
EPA, 2019a, section 5.2.13).
ii. Short-Term PM2.5 Exposures
The 2009 ISA (U.S. EPA, 2009a)
concluded that a ‘‘causal relationship is
likely to exist’’ between short-term
PM2.5 exposure and respiratory effects.
This conclusion was based mainly on
the epidemiologic evidence
demonstrating positive associations
with various respiratory effects.
Specifically, the 2009 ISA described
epidemiologic evidence as consistently
showing PM2.5-associated increases in
hospital admissions and ED visits for
COPD and respiratory infection among
adults or people of all ages, as well as
increases in respiratory mortality. These
results were supported by studies
reporting associations with increased
respiratory symptoms and decreases in
lung function in children with asthma,
though the epidemiologic evidence was
inconsistent for hospital admissions or
emergency department visits for asthma.
Studies examining copollutant models
showed that PM2.5 associations with
respiratory effects were robust to
inclusion of CO or SO2 in the model, but
often were attenuated (though still
positive) with inclusion of O3 or NO2. In
addition to the copollutant models,
evidence supporting an independent
effect of PM2.5 exposure on the
respiratory system was provided by
animal toxicological studies of PM2.5
CAPs demonstrating changes in some
pulmonary function parameters, as well
as inflammation, oxidative stress,
injury, enhanced allergic responses, and
reduced host defenses. Many of these
effects have been implicated in the
pathophysiology for asthma
exacerbation, COPD exacerbation, or
respiratory infection. In the few
controlled human exposure studies
conducted in individuals with asthma
or COPD, PM2.5 exposure mostly had no
effect on respiratory symptoms, lung
function, or pulmonary inflammation.
Available studies in healthy people also
did not clearly demonstrate respiratory
effects following short-term PM2.5
exposures.
Epidemiologic studies evaluated in
the 2019 ISA continue to provide strong
evidence for a relationship between
short-term PM2.5 exposure and several
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respiratory-related endpoints, including
asthma exacerbation (U.S. EPA, 2019a,
section 5.1.2.1), COPD exacerbation
(U.S. EPA, 2019a, section 5.1.4.1), and
combined respiratory-related diseases
(U.S. EPA, 2019a, section 5.1.6),
particularly from studies examining ED
visits and hospital admissions. The
generally positive associations between
short-term PM2.5 exposure and asthma
and COPD as well as ED visits and
hospital admissions are supported by
epidemiologic studies demonstrating
associations with other respiratoryrelated effects such as symptoms and
medication use that are indicative of
asthma and COPD exacerbations (U.S.
EPA, 2019a, sections 5.1.2.2 and
5.4.1.2). The collective body of
epidemiologic evidence for asthma
exacerbation is more consistent in
children than in adults. Additionally,
epidemiologic studies examining the
relationship between short-term PM2.5
exposure and respiratory mortality
provide evidence of consistent positive
associations, demonstrating a
continuum of effects (U.S. EPA, 2019a,
section 5.1.9).
Building off the studies evaluated in
the 2009 ISA, epidemiologic studies
evaluated in the 2019 ISA expand the
assessment of potential copollutant
confounding. There is some evidence
that PM2.5 associations with asthma
exacerbation, combined respiratoryrelated diseases, and respiratory
mortality remain relatively unchanged
in copollutant models with gaseous
pollutants (i.e., O3, NO2, SO2, with more
limited evidence for CO) and other
particle sizes (i.e., PM10–2.5) (U.S. EPA,
2019a, section 5.1.10.1).
In the 2019 ISA, the uncertainty
related to whether there is an
independent effect of PM2.5 on
respiratory health is also partially
addressed by findings from animal
toxicological studies. Specifically, shortterm exposure to PM2.5 enhanced
asthma-related responses in an animal
model of allergic airways disease and
enhanced lung injury and inflammation
in an animal model of COPD (U.S. EPA,
2019a, sections 5.1.2.4.4 and 5.1.4.4.3).
The experimental evidence provides
biological plausibility for some
respiratory-related endpoints, including
limited evidence of altered host defense
and greater susceptibility to bacterial
infection as well as consistent evidence
of respiratory irritant effects. Animal
toxicological evidence for other
respiratory effects is inconsistent and a
recent study by Wyatt et al. (2020) that
was evaluated in the ISA Supplement,
conducted at near ambient PM2.5
concentrations, adds to the limited
evidence base of controlled human
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exposure studies. The study, completed
in healthy young adults subject to
intermittent exercise, found some
significant respiratory effects (including
decrease in lung function), however
these findings were inconsistent with
the controlled human exposure studies
evaluated in the 2019 ISA (U.S. EPA,
2019a, section 5.1.7.2, 5.1.2.3, and
6.1.11.2.1).
The 2019 ISA concludes that ‘‘[t]he
strongest evidence of an effect of shortterm PM2.5 exposure on respiratory
effects is provided by epidemiologic
studies of asthma and COPD
exacerbation. While animal
toxicological studies provide biological
plausibility for these findings, some
uncertainty remains with respect to the
independence of PM2.5 effects’’ (U.S.
EPA, 2019a, p. 5–155). When taken
together, the 2019 ISA concludes that
this evidence ‘‘is sufficient to conclude
that a causal relationship is likely to
exist between short-term PM2.5 exposure
and respiratory effects’’ (U.S. EPA,
2019a, p. 5–155).
d. Cancer
The 2009 ISA concluded that the
overall body of evidence was
‘‘suggestive of a causal relationship
between relevant PM2.5 exposures and
cancer’’ (U.S. EPA, 2009a). This
conclusion was based primarily on
positive associations observed in a
limited number of epidemiologic
studies of lung cancer mortality. The
few epidemiologic studies that had
evaluated PM2.5 exposure and lung
cancer incidence or cancers of other
organs and systems generally did not
show evidence of an association.
Toxicological studies did not focus on
exposures to specific PM size fractions,
but rather investigated the effects of
exposures to total ambient PM, or other
source-based PM such as wood smoke.
Collectively, results of in vitro studies
were consistent with the larger body of
evidence demonstrating that ambient
PM and PM from specific combustion
sources are mutagenic and genotoxic.
However, animal inhalation studies
found little evidence of tumor formation
in response to chronic exposures. A
small number of studies provided
preliminary evidence that PM exposure
can lead to changes in methylation of
DNA, which may contribute to
biological events related to cancer.
Since the completion of the 2009 ISA,
additional cohort studies provide
evidence that long-term PM2.5 exposure
is positively associated with lung cancer
mortality and with lung cancer
incidence, and provide initial evidence
for an association with reduced cancer
survival (U.S. EPA, 2019a, section
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10.2.5). Re-analyses of the ACS cohort
using different years of PM2.5 data and
follow up, along with various exposure
assignment approaches, provide
consistent evidence of positive
associations between long-term PM2.5
exposure and lung cancer mortality
(U.S. EPA, 2019a, Figure 10–3).
Additional support for positive
associations with lung cancer mortality
is provided by recent epidemiologic
studies using individual level data to
control for smoking status, by studies of
people who have never smoked (though
such studies generally report wide
confidence intervals due to the small
number of lung cancer mortality cases
within this population), and in analyses
of cohorts that relied upon proxy
measures to account for smoking status
(U.S. EPA, 2019a, section 10.2.5.1.1).
Although studies that evaluate lung
cancer incidence, including studies of
people who have never smoked, are
limited in number, studies in the 2019
ISA generally report positive
associations with long-term PM2.5
exposures (U.S. EPA, 2019a, section
10.2.5.1.2). A subset of the studies
focusing on lung cancer incidence also
examined histological subtype,
providing some evidence of positive
associations for adenocarcinomas, the
predominate subtype of lung cancer
observed in people who have never
smoked (U.S. EPA, 2019a, section
10.2.5.1.2). Associations between longterm PM2.5 exposure and lung cancer
incidence were found to remain
relatively unchanged, though in some
cases confidence intervals widened, in
analyses that attempted to reduce
exposure measurement error by
accounting for length of time at
residential address or by examining
different exposure assignment
approaches (U.S. EPA, 2019a, section
10.2.5.1.2).
The 2019 ISA evaluates the degree to
which epidemiologic studies have
addressed the potential for confounding
by copollutants and the shape of the C–
R relationship. To date, relatively few
studies have evaluated the potential for
copollutant confounding of the
relationship between long-term PM2.5
exposure and lung cancer mortality or
incidence. A small number of such
studies have generally focused on O3
and report that PM2.5 associations
remain relatively unchanged in
copollutant models (U.S. EPA, 2019a,
section 10.2.5.1.3). However, available
studies have not systematically
evaluated the potential for copollutant
confounding by other gaseous pollutants
or by other particle size fractions (U.S.
EPA, 2019a, section 10.2.5.1.3).
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Compared to total (non-accidental)
mortality (U.S. EPA, 2019a, section
10.2.4.1.4), fewer studies have examined
the shape of the C–R curve for causespecific mortality outcomes, including
lung cancer. Several studies of lung
cancer mortality and incidence have
reported no evidence of deviations from
linearity in the shape of the C–R
relationship (Lepeule et al., 2012;
Raaschou-Nielsen et al., 2013; Puett et
al., 2014), though authors provided only
limited discussions of results (U.S. EPA,
2019a, section 10.2.5.1.4).
In support of the biological
plausibility of an independent effect of
PM2.5 on lung cancer, the 2019 ISA
notes evidence from experimental and
epidemiologic studies demonstrating
that PM2.5 exposure can lead to a range
of effects indicative of mutagenicity,
genotoxicity, and carcinogenicity, as
well as epigenetic effects (U.S. EPA,
2019a, section 10.2.7). For example,
both in vitro and in vivo toxicological
studies have shown that PM2.5 exposure
can result in DNA damage (U.S. EPA,
2019a, section 10.2.2). Although such
effects do not necessarily equate to
carcinogenicity, the evidence that PM
exposure can damage DNA, and elicit
mutations, provides support for the
plausibility of epidemiologic
associations with lung cancer mortality
and incidence. Additional supporting
studies indicate the occurrence of
micronuclei formation and
chromosomal abnormalities (U.S. EPA,
2019a, section 10.2.2.3), and differential
expression of genes that may be relevant
to cancer pathogenesis, following PM
exposures. Experimental and
epidemiologic studies that examine
epigenetic effects indicate changes in
DNA methylation, providing some
support for PM2.5 exposure contributing
to genomic instability (U.S. EPA, 2019a,
section 10.2.3). Overall, there is limited
evidence that long-term PM2.5 exposure
is associated with cancers in other organ
systems, but there is some evidence that
PM2.5 exposure may reduce survival in
individuals with cancer (U.S. EPA,
2019a, section 10.2.7; U.S. EPA, 2022a,
section 2.1.1.4.1).
Epidemiologic evidence for
associations between PM2.5 and lung
cancer mortality and incidence, together
with evidence supporting the biological
plausibility of such associations,
contributes to the 2019 ISA’s conclusion
that the evidence ‘‘is sufficient to
conclude that a causal relationship is
likely to exist between long-term PM2.5
exposure and cancer’’ (U.S. EPA, 2019,
section 10.2.7).
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e. Nervous System Effects
Reflecting the very limited evidence
available in the 2012 review, the 2009
ISA did not make a causality
determination for long-term PM2.5
exposures and nervous system effects
(U.S. EPA, 2009c). Since the 2012
review, this body of evidence has grown
substantially (U.S. EPA, 2019, section
8.2). Animal toxicological studies
assessed in in the 2019 ISA report that
long-term PM2.5 exposures can lead to
morphologic changes in the
hippocampus and to impaired learning
and memory. This evidence is
consistent with epidemiologic studies
reporting that long-term PM2.5 exposure
is associated with reduced cognitive
function (U.S. EPA, 2019a, section
8.2.5). Further, while the evidence is
limited, the presence of early markers of
Alzheimer’s disease pathology has been
demonstrated in rodents following longterm exposure to PM2.5 CAPs. These
findings support reported associations
with neurodegenerative changes in the
brain (i.e., decreased brain volume), allcause dementia, or hospitalization for
Alzheimer’s disease in a small number
of epidemiologic studies (U.S. EPA,
2019a, section 8.2.6). Additionally, loss
of dopaminergic neurons in the
substantia nigra, a hallmark of
Parkinson disease, has been reported in
mice (U.S. EPA, 2019a, section 8.2.4),
though epidemiologic studies provide
only limited support for associations
with Parkinson’s disease (U.S. EPA,
2019a, section 8.2.6). Overall, the lack of
consideration of copollutant
confounding introduces some
uncertainty in the interpretation of
epidemiologic studies of nervous system
effects, but this uncertainty is partly
addressed by the evidence for an
independent effect of PM2.5 exposures
provided by experimental animal
studies.
In addition to the findings described
above, which are most relevant to older
adults, several studies of
neurodevelopmental effects in children
have also been conducted. Positive
associations between long-term
exposure to PM2.5 during the prenatal
period and autism spectrum disorder
(ASD) are observed in multiple
epidemiologic studies (U.S. EPA, 2019a,
section 8.2.7.2), while studies of
cognitive function provide little support
for an association (U.S. EPA, 2019a,
section 8.2.5.2). Interpretation of these
epidemiologic studies is limited due to
the small number of studies, their lack
of control for potential confounding by
copollutants, and uncertainty regarding
the critical exposure windows.
Biological plausibility is provided for
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the ASD findings by a study in mice that
found inflammatory and morphologic
changes in the corpus collosum and
hippocampus, as well as
ventriculomegaly (i.e., enlarged lateral
ventricles) in young mice following
prenatal exposure to PM2.5 CAPs.
Taken together, the 2019 ISA
concludes that studies indicate longterm PM2.5 exposures can lead to effects
on the brain associated with
neurodegeneration (i.e.,
neuroinflammation and reductions in
brain volume), as well as cognitive
effects in older adults (U.S. EPA, 2019a,
Table 1–2). Animal toxicological studies
provide evidence for a range of nervous
system effects in adult animals,
including neuroinflammation and
oxidative stress, neurodegeneration, and
cognitive effects, and effects on
neurodevelopment in young animals.
The epidemiologic evidence is more
limited, but studies generally support
associations between long-term PM2.5
exposure and changes in brain
morphology, cognitive decrements and
dementia. There is also initial, and
limited, evidence for
neurodevelopmental effects, particularly
ASD. The consistency and coherence of
the evidence supports the 2019 ISA’s
conclusion that ‘‘the collective evidence
is sufficient to conclude that a causal
relationship is likely to exist between
long-term PM2.5 exposure and nervous
system effects’’ (U.S. EPA, 2019a,
section 8.2.9).
f. Other Effects
For other health effect categories that
were evaluated for their relationship
with PM2.5 exposures (i.e., short-term
PM2.5 exposure and nervous system
effects and short- and long-term PM2.5
exposure and metabolic effects,
reproduction and fertility, and
pregnancy and birth outcomes (U.S.
EPA, 2022a, Table ES–1), the currently
available evidence is ‘‘suggestive of, but
not sufficient to infer, a causal
relationship,’’ mainly due to
inconsistent evidence across specific
outcomes and uncertainties regarding
exposure measurement error, the
potential for confounding, and potential
modes of action (U.S. EPA, 2019a,
sections 7.14, 7.2.10, 8.1.6, and 9.1.5).
The causality determination for shortterm PM2.5 exposure and nervous
system effects in the 2019 ISA reflects
a revision to the causality determination
in the 2009 ISA from ‘‘inadequate to
infer a causal relationship,’’ while this
is the first time assessments of causality
were conducted for long-term PM2.5
exposure and nervous system effects, as
well as short- and long-term PM2.5
exposure and metabolic effects reflect.
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Recent studies evaluated in the 2019
ISA also further explored the
relationship between short-and longterm ultrafine particle (UFP) exposure
and health effects. (i.e., cardiovascular
effects and short-term UFP exposures;
respiratory effects and short-term UFP
exposures; and nervous system effects
and long- and short-term exposures
(U.S. EPA, 2022a, Table ES–1). The
currently available evidence is
‘‘suggestive of, but not sufficient to
infer, a causal relationship’’ for shortterm UFP exposure and cardiovascular
and respiratory effects and for shortand long-term UFP exposure and
nervous system effects, primarily due to
uncertainties and limitations in the
evidence, specifically, variability across
studies in the definition of UFPs and the
exposure metric used (U.S. EPA, 2019a,
P.3.1; U.S. EPA, 2022a, section
3.3.1.6.3). The causality determinations
for the other health effect categories
evaluated in the 2019 ISA are
‘‘inadequate to infer a causal
relationship.’’ Additionally, this is the
first time assessments of causality were
conducted for short- and long-term UFP
exposure and metabolic effects and
long-term UFP exposure and nervous
system effects (U.S. EPA, 2022a, Table
ES–1).
With the advent of the global COVID–
19 pandemic, a number of recent studies
evaluated in the ISA Supplement
examined the relationship between
ambient air pollution, specifically PM2.5,
and SARS–CoV–2 infections and
COVID–19 deaths, including a few
studies within the U.S. and Canada
(U.S. EPA, 2022a, section 3.3.2).59 Some
studies examined whether daily changes
in PM2.5 can influence SARS–CoV–2
infection and COVID–19 death (U.S.
EPA, 2022a, section 3.3.2.1).
Additionally, several studies evaluated
59 While there is no exact corollary within the
2019 ISA for these types of studies, the 2019 ISA
presented evidence that evaluates the potential
relationship between short- and long-term PM2.5
exposure and respiratory infection (U.S. EPA,
2022a, section 5.1.5 and 5.2.6). Studies assessed in
the 2019 ISA report some evidence of positive
associations between short-term PM2.5 and hospital
admissions and ED visits for respiratory infections,
however the interpretation of these studies is
complicated by the variability in the type of
respiratory infection outcome examined (U.S. EPA,
2022a, Figure 5–7). In the 2019 ISA, studies of longterm PM2.5 exposure were limited and while there
were some positive associations reported, there was
minimal overlap in respiratory infection outcomes
examined across studies. Exposure to PM2.5 has
been shown to impair host defense, specifically
altering macrophage function, providing a
biological pathway by which PM2.5 exposure could
lead to respiratory infection (U.S. EPA, 2022a,
sections 5.1.1 and 5.1.5.) There is some additional
evidence that PM2.5 exposure can lead to decreases
in an individual’s immune response, which can
subsequently facilitate replication of respiratory
viruses (Bourdrel et al., 2021).
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whether long-term PM2.5 exposure
increases the risk of SARS–CoV–2
infection and COVID–19 death in North
America (U.S. EPA, 2022a, section
3.3.2.2). While there is initial evidence
of positive associations with SARS–
CoV–2 infection and COVID–19 death,
uncertainties remain due to
methodological issues that may
influence the results, including: (1) the
use of ecological study design; (2)
studies were conducted during the
ongoing pandemic when the etiology of
COVID–19 was still not well understood
(e.g., specifically, there are important
differences in COVID–19-related
outcomes by a variety of factors such as
race and SES); and (3) studies did not
account for crucial factors that could
influence results (e.g., stay-at-home
orders, social distancing, use of masks,
and testing capacity) (U.S. EPA, 2022a,
chapter 5). Taken together, while there
is initial evidence of positive
associations with SARS–CoV–2
infection and COVID–19 death,
uncertainties remain due to
methodological issues.
2. Public Health Implications and AtRisk Populations
The public health implications of the
evidence regarding PM2.5-related health
effects, as for other effects, are
dependent on the type and severity of
the effects, as well as the size of the
population affected. Such factors are
discussed here in the context of our
consideration of the health effects
evidence related to PM2.5 in ambient air.
This section also summarizes the
current information on population
groups at increased risk of the effects of
PM2.5 in ambient air.
The information available in this
reconsideration has not altered our
understanding of human populations at
risk of health effects from PM2.5
exposures. As recognized in the 2020
review, the 2019 ISA cites extensive
evidence indicating that ‘‘both the
general population as well as specific
populations and lifestages are at risk for
PM2.5-related health effects’’ (U.S. EPA,
2019a, p. 12–1). Factors that may
contribute to increased risk of PM2.5related health effects include lifestage
(children and older adults), pre-existing
diseases (cardiovascular disease and
respiratory disease), race/ethnicity, and
SES.60
Children make up a substantial
fraction of the U.S. population, and
often have unique factors that contribute
60 As described in the 2019 ISA, other factors that
have the potential to contribute to increased risk
include obesity, diabetes, genetic factors, smoking
status, sex, diet, and residential location (U.S. EPA,
2019, chapter 12).
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to their increased risk of experiencing a
health effect due to exposures to
ambient air pollutants because of their
continuous growth and development.61
Children may be particularly at risk for
health effects related to ambient PM2.5
exposures compared with adults
because they have (1) a developing
respiratory system, (2) increased
ventilation rates relative to body mass
compared with adults, and (3) an
increased proportion of oral breathing,
particularly in boys, relative to adults
(U.S. EPA, 2019a, section 12.5.1.1).
There is strong evidence that
demonstrates PM2.5 associated health
effects in children, particularly from
epidemiologic studies of long-term
PM2.5 exposure and impaired lung
function growth, decrements in lung
function, and asthma development.
However, there is limited evidence from
stratified analyses that children are at
increased risk of PM2.5-related health
effects compared to adults.
Additionally, there is some evidence
that indicates that children receive
higher PM2.5 exposures than adults, and
dosimetric differences in children
compared to adults can contribute to
higher doses (U.S. EPA, 2019a, section
12.5.1.1).
In the U.S., older adults, often defined
as adults 65 years of age and older,
represent an increasing portion of the
population and often have pre-existing
diseases or conditions that may
compromise biological function. While
there is limited evidence to indicate that
older adults have higher exposures than
younger adults, older adults may receive
higher doses of PM2.5 due to dosimetric
differences. There is consistent evidence
from studies of older adults
demonstrating generally consistent
positive associations in studies
examining health effects from short- and
long-term PM2.5 exposure and
cardiovascular or respiratory hospital
admissions, emergency department
visits, or mortality (U.S. EPA, 2019a,
sections 6.1, 6.2, 11.1, 11.2, 12.5.1.2).
Additionally, several animal
toxicological, controlled human
exposure, and epidemiologic studies did
not stratify results by lifestage, but
instead focused the analyses on older
individuals, and can provide coherence
and biological plausibility for the
occurrence among this lifestage (U.S.
EPA, 2019a, section 12.5.1.2).
Individuals with pre-existing disease
may be considered at greater risk of an
air pollution-related health effect than
those without disease because they are
likely in a compromised biological state
61 Children, as used throughout this document,
generally refers to those younger than 18 years old.
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that can vary depending on the disease
and severity. With regard to
cardiovascular disease, we first note that
cardiovascular disease is the leading
cause of death in the U.S., accounting
for one in four deaths, and
approximately 12% of the adult
population in the U.S. has a
cardiovascular disease (U.S. EPA,
2019a, section 12.3.1). Strong evidence
demonstrates that there is a causal
relationship between cardiovascular
effects and long- and short-term
exposures to PM2.5. Some of the
evidence supporting this conclusion is
from studies of panels or cohorts with
pre-existing cardiovascular disease,
which provide supporting evidence but
do not directly demonstrate an
increased risk (U.S. EPA, 2019a, section
12.3.1). Epidemiologic evidence
indicates that individuals with preexisting cardiovascular disease may be
at increased risk for PM2.5-associated
health effects compared to those
without pre-existing cardiovascular
disease. While the evidence does not
consistently support increased risk for
all pre-existing cardiovascular diseases,
there is evidence that certain preexisting cardiovascular diseases (e.g.,
hypertension) may be a factor that
increases PM2.5-related risk.
Furthermore, there is strong evidence
supporting a causal relationship for
long- and short-term PM2.5 exposure and
cardiovascular effects, particularly for
IHD (U.S. EPA, 2019a, chapter 6, section
12.3.1).
With regard to respiratory disease, we
first note that the most chronic
respiratory diseases in the U.S. are
asthma and COPD. Asthma affects a
substantial fraction of the U.S.
population and is the leading chronic
disease among children. COPD
primarily affects older adults and
contributes to compromised respiratory
function and underlying pulmonary
inflammation. The body of evidence
indicates that individuals with preexisting respiratory diseases,
particularly asthma and COPD, may be
at increased risk for PM2.5-related health
effects compared to those without preexisting respiratory diseases (U.S. EPA,
2019a, section 12.3.5). There is strong
evidence indicating PM2.5-associated
respiratory effects among those with
asthma which forms the primary
evidence base for the likely to be causal
relationship between short-term
exposures to PM2.5 and respiratory
health effects (U.S. EPA, 2019a, section
12.3.5). For asthma, epidemiologic
evidence demonstrates associations
between short-term PM2.5 exposures and
respiratory effects, particularly evidence
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for asthma exacerbation, and controlled
human exposure and animal
toxicological studies demonstrate
biological plausibility for asthma
exacerbation with PM2.5 exposures (U.S.
EPA, 2019a, section 12.3.5.1). For
COPD, epidemiologic studies report
positive associations between short-term
PM2.5 exposures and hospital
admissions and emergency department
visits for COPD, with supporting
evidence from panel studies
demonstration COPD exacerbation.
Epidemiologic evidence is supported by
some experimental evidence of COPDrelated effects, which provides support
for the biological plausibility for COPD
in response to PM2.5 exposures (U.S.
EPA, 2019a, section 12.3.5.2).
There is strong evidence for racial and
ethnic disparities in PM2.5 exposures
and PM2.5- related health risk, as
assessed in the 2019 ISA and with even
more evidence available since the
literature cutoff date for the 2019 ISA
and evaluated in the ISA Supplement.
There is strong evidence demonstrating
that Black and Hispanic populations, in
particular, have higher PM2.5 exposures
than non-Hispanic White populations
(U.S. EPA, 2019a, Figure 12–2; U.S.
EPA, 2022a, Figure 3–38). Black
populations or individuals that live in
predominantly Black neighborhoods
experience higher PM2.5 exposures, in
comparison to non-Hispanic White
populations. There is also consistent
evidence across multiple studies that
demonstrate increased risk of PM2.5related health effects, with the strongest
evidence for health risk disparities for
mortality (U.S. EPA, 2019a, section
12.5.4). There is also evidence of health
risk disparities for both Hispanic and
non-Hispanic Black populations
compared to non-Hispanic White
populations for cause-specific mortality
and incident hypertension (U.S. EPA,
2022a, section 3.3.3.2).
Socioeconomic status (SES) is a
composite measure that includes
metrics such as income, occupation, or
education, and can play a role in access
to healthy environments as well as
access to healthcare. SES may be a
factor that contributes to differential risk
from PM2.5- related health effects.
Studies assessed in the 2019 ISA and
ISA Supplement provide evidence that
lower SES communities are exposed to
higher concentrations of PM2.5
compared to higher SES communities
(U.S. EPA, 2019a, section 12.5.3; U.S.
EPA, 2022a, section 3.3.3.1.1). Studies
using composite measures of
neighborhood SES consistently
demonstrated a disparity in both PM2.5
exposure and the risk of PM2.5-related
health outcomes. There is some
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evidence that supports associations
larger in magnitude between mortality
and long-term PM2.5 exposures for those
with low income or living in lower
income areas compared to those with
higher income or living in higher
income neighborhoods (U.S. EPA,
2019a, section 12.5.3; U.S. EPA, 2022a,
section 3.3.3.1.1). Additionally,
evidence supports conclusions that
lower SES is associated with causespecific mortality and certain health
endpoints (i.e., MI and CHF), but less so
for all-cause or total (non-accidental)
mortality (U.S. EPA, 2022a, section
3.3.3.1).
The magnitude and characterization
of a public health impact is dependent
upon the size and characteristics of the
populations affected, as well as the type
or severity of the effects. As summarized
above, lifestage (children and older
adults), race/ethnicity and SES are
factors that increase the risk of PM2.5related health effects. The American
Community Survey (ACS) for 2019
estimates that approximately 22% and
16% of the U.S. population are children
(age <18) and older adults (age 65+),
respectively. For all ages, non-Hispanic
Black and Hispanic populations are
approximately 12% and 18% of the
overall U.S. population in 2019.
Currently available information that
helps to characterize key features of
these population is included in the PA
(U.S. EPA, 2022b, Table 3–2).
As noted above, individuals with preexisting cardiovascular disease and preexisting respiratory disease may also be
at increased risk of PM2.5-related health
effects. Currently available information
that helps to characterize key features of
populations with cardiovascular or
respiratory diseases or conditions is
included in the PA (U.S. EPA, 2022b,
Table 3–3). The National Center for
Health Statistics data for 2018 indicate
that, for adult populations, older adults
(e.g., those 65 years and older) have a
higher prevalence of cardiovascular
diseases compared to younger adults
(e.g., those 64 years and younger). For
respiratory diseases, older adults also
have a higher prevalence of emphysema
than younger adults, and adults 44 years
or older have a higher prevalence of
chronic bronchitis. However, the
prevalence for asthma is generally
similar across all adult age groups.
With respect to race, American
Indians or Alaskan Natives have the
highest prevalence of all heart disease
and coronary heart disease, while
Blacks have the highest prevalence of
hypertension and stroke. Hypertension
has the highest prevalence across all
racial groups compared to other
cardiovascular diseases or conditions,
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ranging from approximately 22% to
32% of each racial group. Overall, the
prevalence of cardiovascular diseases or
conditions is lowest for Asians
compared to Whites, Blacks, and
American Indians or Alaskan Natives.
Asthma prevalence is highest among
Black and American Indian or Alaska
Native populations, while prevalence is
generally similar across racial groups for
chronic bronchitis and emphysema.
Overall, the prevalence for respiratory
diseases is lowest for Asians compared
to Whites, Blacks, and American
Indians or Alaskan Natives. With regard
to ethnicity, cardiovascular and
respiratory disease prevalence across all
diseases or conditions is generally
similar between Hispanic and nonHispanic populations, although nonHispanics have a slightly higher
prevalence compared to Hispanics.
Taken together, this information
indicates that the groups at increased
risk of PM2.5-related health effects
represent a substantial portion of the
total U.S. population. In evaluating the
primary PM2.5 standards, an important
consideration is the potential PM2.5related public health impacts in these
populations.
3. PM2.5 Concentrations in Key Studies
Reporting Health Effects
To inform conclusions on the
adequacy of the public health protection
provided by the current primary PM2.5
standards, the sections below
summarize the PA’s evaluation of the
PM2.5 exposure concentrations that have
been examined in controlled human
exposure studies, animal toxicological
studies, and epidemiologic studies. The
PA places the greatest emphasis on the
health outcomes for which the 2019 ISA
concludes that the evidence supports a
‘‘causal’’ or a ‘‘likely to be causal’’
relationship with PM2.5 exposures (U.S.
EPA, 2022b, section 3.3.3). As described
in greater detail in section II.B.1 above,
this includes mortality, cardiovascular
effects, and respiratory effects
associated with short- or long-term
PM2.5 exposures and cancer and nervous
system effects associated with long-term
PM2.5 exposures. While the causality
determinations in the 2019 ISA are
informed by studies evaluating a wide
range of PM2.5 concentrations, the
sections below summarize the
considerations in the PA regarding the
degree to which the evidence assessed
in the 2019 ISA and ISA Supplement
supports the occurrence of PM-related
health effects at concentrations relevant
to informing conclusions on the primary
PM2.5 standards.
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a. PM2.5 Exposure Concentrations
Evaluated in Experimental Studies
Evidence for a particular PM2.5-related
health outcome is strengthened when
results from experimental studies
demonstrate biologically plausible
mechanisms through which adverse
human health outcomes could occur
(U.S. EPA, 2015, Preamble p. 20). Two
types of experimental studies are of
particular importance in understanding
the effects of PM exposures: controlled
human exposure and animal
toxicological studies. In such studies,
investigators expose human volunteers
or laboratory animals, respectively, to
known concentrations of air pollutants
under carefully regulated environmental
conditions and activity levels. Thus,
controlled human exposure and animal
toxicological studies can provide
information on the health effects of
experimentally administered pollutant
exposures under highly controlled
laboratory conditions (U.S. EPA, 2015,
Preamble, p. 11).
Controlled human exposure studies
have reported that PM2.5 exposures
lasting from less than one hour up to
five hours can impact cardiovascular
function,62 and the most consistent
evidence from these studies is for
impaired vascular function (U.S. EPA,
2019a, section 6.1.13.2). In addition,
although less consistent, the 2019 ISA
notes that studies examining PM2.5
exposures also provide evidence for
increased blood pressure (U.S. EPA,
2019a, section 6.1.6.3), conduction
abnormalities/arrhythmia (U.S. EPA,
2019a, section 6.1.4.3), changes in heart
rate variability (U.S. EPA, 2019a, section
6.1.10.2), changes in hemostasis that
could promote clot formation (U.S. EPA,
2019a, section 6.1.12.2), and increases
in inflammatory cells and markers (U.S.
EPA, 2019a, section 6.1.11.2). The 2019
ISA concludes that, when taken as a
whole, controlled human exposure
studies demonstrate that short-term
exposure to PM2.5 may impact
cardiovascular function in ways that
could lead to more serious outcomes
(U.S. EPA, 2019a, section 6.1.16). Thus,
such studies can provide insight into
the potential for specific PM2.5
exposures to result in physiological
changes that could increase the risk of
more serious effects.
Table 3–4 in the PA summarizes
information from the 2019 ISA on
available controlled human exposure
62 In contrast, controlled human exposure studies
provide little evidence for respiratory effects
following short-term PM2.5 exposures (U.S. EPA,
2019a, section 5.1, Table 5–18). Therefore, this
section focuses on cardiovascular effects evaluated
in controlled human exposure studies of PM2.5
exposure.
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studies the evaluate effects on markers
of cardiovascular function following
exposure to PM2.5 (U.S. EPA, 2022b).
Most of the controlled human exposure
studies in Table 3–4 in the PA have
evaluated average PM2.5 concentrations
at or above about 100 mg/m3, with
exposure durations typically up to about
two hours. Statistically significant
effects on one or more indicators of
cardiovascular function are often,
though not always, reported following
2-hour exposures to average PM2.5
concentrations at and above about 120
mg/m3, with less consistent evidence for
effects following exposures to
concentrations lower than 120 mg/m3.
Impaired vascular function, the effect
identified in the 2019 ISA as the most
consistent across studies (U.S. EPA,
2019a, section 6.1.13.2) is shown
following 2-hour exposures to PM2.5
concentrations at and above 149 mg/m3.
Mixed results are reported in the studies
that evaluated longer exposure
durations (i.e., longer than 2 hours) and
lower (i.e., near-ambient) PM2.5
concentrations (U.S. EPA, 2022b,
section 3.3.3.1). For example, significant
effects for some outcomes were reported
following 5-hour exposures to 24 mg/m3
in Hemmingsen et al. (2015b), but not
for other outcomes following 5-hour
exposures to 24 mg/m3 in Hemmingsen
et al. (2015a) and not following 24-hour
exposures to 10.5 mg/m3 in Bra¨uner et
al. (2008). Additionally, Wyatt et al.
(2020) found significant effects for some
cardiovascular (e.g., systematic
inflammation markers, cardiac
repolarization, and decreased
pulmonary function) effects following 4hour exposures to 37.8 mg/m3 in healthy
young participants (18–35 years, n=21)
who were subject to intermittent
moderate exercise. The higher
ventilation rate and longer exposure
duration in this study compared to most
controlled human exposure studies is
roughly equivalent to a 2-hour exposure
of 75–100 mg/m3 of PM2.5. Therefore,
dosimetric considerations may explain
the observed changes in inflammation
in young healthy individuals. Though
this study provides evidence of some
effects at lower PM2.5 concentrations,
overall there is inconsistent evidence for
inflammation in other controlled human
exposure studies evaluated in the 2019
ISA (U.S. EPA, 2019a, sections 5.1.7.,
5.1.2.3.3, and 6.1.11.2.1; U.S. EPA,
2022a, section 3.3.1).
While controlled human exposure
studies are important in establishing
biological plausibility, it is unclear how
the results from these studies alone and
the importance of the effects observed in
these studies, should be interpreted
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5593
with respect to adversity to public
health. More specifically, impaired
vascular function can signal an
intermediate effect along the potential
biological pathways for cardiovascular
effects following short-term exposure to
PM2.5 and show a role for exposure to
PM2.5 leading to potential worsening of
IHD and heart failure followed
potentially by ED visits, hospital
admissions, or mortality (U.S. EPA,
2019, section 6.1 and Figure 6–1).
However, just observing the occurrence
of impaired vascular function alone
does not clearly suggest an adverse
health outcome. Additionally,
associated judgments regarding
adversity or health significance of
measurable physiological responses to
air pollutants have been informed by
guidance, criteria or interpretative
statements developed within the public
health community, including the
American Thoracic Society (ATS) and
the European Respiratory Society (ERS),
which cooperatively updated the ATS
2000 statement What Constitutes an
Adverse Health Effect of Air Pollution
(ATS, 2000) with new scientific
findings, including the evidence related
to air pollution and the cardiovascular
system (Thurston et al., 2017).63 With
regard to vascular function, the ATS/
ERS statement considers the adversity of
both chronic and acute reductions in
endothelial function. While the ATS/
ERS statement concluded that chronic
endothelial and vascular dysfunction
can be judged to be a biomarker of an
adverse health effect from air pollution,
they also conclude that ‘‘the health
relevance of acute reductions in
endothelial function induced by air
pollution is less certain’’ (Thurston et
al., 2017). This is particularly
informative to our consideration of the
controlled human exposure studies
which are short-term in nature (i.e.,
ranging from 2- to 5-hours), including
63 The ATS/ERS described its 2017 statement as
one ‘‘intended to provide guidance to policymakers,
clinicians and public health professionals, as well
as others who interpret the scientific evidence on
the health effects of air pollution for risk
management purposes’’ and further notes that
‘‘considerations as to what constitutes an adverse
health effect, in order to provide guidance to
researchers and policymakers when new health
effects markers or health outcome associations
might be reported in future.’’ The most recent
policy statement by the ATS, which once again
broadens its discussion of effects, responses and
biomarkers to reflect the expansion of scientific
research in these areas, reiterates that concept,
conveying that it does not offer ‘‘strict rules or
numerical criteria, but rather proposes
considerations to be weighed in setting boundaries
between adverse and nonadverse health effects,’’
providing a general framework for interpreting
evidence that proposes a ‘‘set of considerations that
can be applied in forming judgments’’ for this
context (Thurston et al., 2017).
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those studies that are conducted at nearambient PM2.5 concentrations.
The PA also notes that it is important
to recognize that controlled human
exposure studies include a small
number of individuals compared to
epidemiologic studies. Additionally,
these studies tend to include generally
healthy adult individuals, who are at a
lower risk of experiencing health effects.
These studies, therefore, often do not
include including children, or older
adults, or individuals with pre-existing
conditions. As such, these studies are
somewhat limited in their ability to
inform at what concentrations effects
may be elicited in at-risk populations.
Nonetheless, to provide some insight
into what these controlled human
exposure studies may indicate regarding
short-term exposure to peak PM2.5
concentrations and how concentrations
relate to ambient PM2.5 concentrations,
analyses in the PA (U.S. EPA, 2022b,
Figure 2–19) examine monitored 2-hour
PM2.5 concentrations (the exposure
window most often utilized in the
controlled human exposure studies) at
sites meeting the current primary PM2.5
standards to evaluate the degree to
which 2-hour ambient PM2.5
concentrations at such locations are
likely to exceed the 2-hour exposure
concentrations in the controlled human
exposure studies at which statistically
significant effects are reported in
multiple studies for one or more
indicators of cardiovascular function. At
sites meeting the current primary PM2.5
standards, most 2-hour concentrations
are below 10 mg/m3, and almost never
exceed 30 mg/m3. The extreme upper
end of the distribution of 2-hour PM2.5
concentrations is shifted higher during
the warmer months (April to
September), generally corresponding to
the period of peak wildfire frequency in
the U.S. At sites meeting the current
primary PM2.5 standards, the highest 2hour concentrations measured tend to
occur during the period of peak wildfire
frequency (i.e., 99.9th percentile of 2hour concentrations is 62 mg/m3 during
the warm season considered as a
whole). Most of the sites measuring
these very high concentrations are in the
northwestern U.S. and California (U.S.
EPA, 2022b, Appendix A, Figure A–1),
where wildfires have been relatively
common in recent years. When the
typical fire season is excluded from the
analysis, the extreme upper end of the
distribution is reduced (i.e., 99.9th
percentile of 2-hour concentrations is 55
mg/m3).64 Given these results, the PA
concludes that PM2.5 exposure
concentrations evaluated in most of
these controlled human exposure
studies are well-above the 2-hour
ambient PM2.5 concentrations typically
measured in locations meeting the
current primary standards.
With respect to animal toxicological
studies, the 2019 ISA relies on animal
toxicological studies to support the
plausibility of a wide range of PM2.5related health effects. While animal
toxicological studies often examine
more severe health outcomes and longer
exposure durations than controlled
human exposure studies, there is
uncertainty in extrapolating the effects
seen in animals, and the PM2.5
exposures and doses that cause those
effects, to human populations. The PA
considers these uncertainties when
evaluating what the available animal
toxicological studies may indicate with
regard to the current primary PM2.5
standards.
As with controlled human exposure
studies, most animal toxicological
studies evaluated in the 2019 ISA have
examined effects following exposure to
PM2.5 well-above the concentrations
likely to be allowed by the current PM2.5
standards. Such studies have generally
examined short-term exposures to PM2.5
concentrations ranging from 100 to
>1,000 mg/m3 and long-term exposures
to concentrations from 66 to >400 mg/m3
(e.g., see U.S. EPA, 2019a, Table 1–2).
Two exceptions are animal toxicological
studies reporting impaired lung
development following long-term
exposures (i.e., 24 hours per day for
several months prenatally and
postnatally) to an average PM2.5
concentration of 16.8 mg/m3 (Mauad et
al., 2008) and increased carcinogenic
potential following long-term exposures
(i.e., 2 months) to an average PM2.5
concentration of 17.7 mg/m3 (Cangerana
Pereira et al., 2011). These two studies
report serious effects following longterm exposures to PM2.5 concentrations
similar to the ambient concentrations
reported in some PM2.5 epidemiologic
studies (U.S. EPA, 2019a, Table 1–2),
though still above the ambient
concentrations likely to occur in areas
meeting the current primary PM2.5
standards. However, noting uncertainty
in extrapolating the effects seen in
animals, and the PM2.5 exposures and
doses that cause those effects to human
populations, animal toxicological
studies are of limited utility in
informing decisions on the public
health protection provided by the
current or alternative primary PM2.5
64 Similar analyses of 4-hour and 5-hour PM
2.5
concentrations are presented in Appendix A, Figure
A–2 and Figure A–3, respectively of the PA (U.S.
EPA, 2022b).
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standards. Therefore, the animal
toxicological studies are most useful in
providing further evidence to support
the biological mechanisms and
plausibility of various adverse effects.
b. Ambient PM2.5 Concentrations in
Locations of Epidemiologic Studies
As summarized in section II.B.1
above, epidemiologic studies examining
associations between daily or annual
average PM2.5 exposures and mortality
or morbidity represent a large part of the
evidence base supporting several of the
2019 ISA’s ‘‘causal’’ and ‘‘likely to be
causal’’ determinations. The PA
considers the ambient PM2.5
concentrations present in areas where
epidemiologic studies have evaluated
associations with mortality or
morbidity, and what such
concentrations may indicate regarding
the adequacy of the primary PM2.5
standards. The use of information from
epidemiologic studies to inform
conclusions on the primary PM2.5
standards is complicated by the fact that
such studies evaluate associations
between distributions of ambient PM2.5
and health outcomes, and do not
identify the specific exposures that can
lead to the reported effects. Rather,
health effects can occur over the entire
distribution of ambient PM2.5
concentrations evaluated, and
epidemiologic studies conducted to date
do not identify a population-level
threshold below which it can be
concluded with confidence that PM2.5associated health effects do not occur.
Therefore, the PA evaluates the PM2.5 air
quality distributions over which
epidemiologic studies support health
effect associations (U.S. EPA, 2022b,
section 3.3.3.2). In the absence of
discernible thresholds, the PA considers
the study-reported ambient PM2.5
concentrations reflecting estimated
exposure with a focus around the
middle portion of the PM2.5 air quality
distribution, where the bulk of the
observed data reside and which
provides the strongest support for
reported health effect associations. The
section below describes the
consideration of the key epidemiologic
studies and observations from these
studies, as evaluated in the PA (U.S.
EPA, 2022b, section 3.3.3.2).
i. PM2.5 Air Quality Distributions
Associated With Mortality or Morbidity
in Key Epidemiologic Studies
As an initial matter, in considering
the PM2.5 air quality distributions
associated with mortality or morbidity
in the key epidemiologic studies, the PA
recognizes that in previous reviews, the
decision framework used to judge
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adequacy of the existing PM2.5
standards, and what levels of any
potential alternative standards should
be considered, placed significant weight
on epidemiologic studies that assessed
associations between PM2.5 exposure
and health outcomes that were most
strongly supported by the body of
scientific evidence. In doing so, the
decision framework recognized that
while there is no specific point in the
air quality distribution of any
epidemiologic study that represents a
‘‘bright line’’ at and above which effects
have been observed and below which
effects have not been observed, there is
significantly greater confidence in the
magnitude and significance of observed
associations for the part of the air
quality distribution corresponding to
where the bulk of the health events in
each study have been observed,
generally at or around the mean
concentration. This is the case both for
studies of daily PM2.5 exposures and for
studies of annual average PM2.5
exposures (U.S. EPA, 2022b, section
3.3.3.2.1).
As discussed further in the PA,
studies of daily PM2.5 exposures
examine associations between day-today variation in PM2.5 concentrations
and health outcomes, often over several
years (U.S. EPA, 2022b, section
3.3.3.2.1). While there can be
considerable variability in daily
exposures over a multi-year study
period, most of the estimated exposures
reflect days with ambient PM2.5
concentrations around the middle of the
air quality distributions examined (i.e.,
‘‘typical’’ days rather than days with
extremely high or extremely low
concentrations). Similarly, for studies of
annual PM2.5 exposures, most of the
health events occur at estimated
exposures that reflect annual average
PM2.5 concentrations around the middle
of the air quality distributions
examined. In both cases, epidemiologic
studies provide the strongest support for
reported health effect associations for
this middle portion of the PM2.5 air
quality distribution, which corresponds
to the bulk of the underlying data, rather
than the extreme upper or lower ends of
the distribution. Consistent with this, as
noted in the PA (U.S. EPA, 2022b,
section 3.3.1.1), several epidemiologic
studies report that associations persist
in analyses that exclude the upper
portions of the distributions of
estimated PM2.5 exposures, indicating
that ‘‘peak’’ PM2.5 exposures are not
disproportionately responsible for
reported health effect associations.
Thus, in considering PM2.5 air quality
data from epidemiologic studies,
consistent with approaches in the 2012
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and 2020 reviews (78 FR 3161, January
15, 2013; U.S. EPA, 2011, sections 2.1.3
and 2.3.4.1; 85 FR 82716–82717,
December 18, 2020; U.S. EPA, 2020a,
sections 3.1.2 and 3.2.3), the PA
evaluates study-reported means (or
medians) of daily and annual average
PM2.5 concentrations as indicators for
the middle portions of the air quality
distributions, over which studies
generally provide strong support for
reported associations and for which
confidence in the magnitude and
significance of associations observed in
the epidemiologic studies is greatest (78
FR 3101, January 15, 2013). In addition
to the overall study means, the PA also
focuses on concentrations somewhat
below the means (e.g., 25th and 10th
percentiles), when such information is
available from the epidemiologic
studies, which again is consistent with
approaches used in previous reviews. In
so doing, the PA notes, as in previous
reviews, that a relatively small portion
of the health events are observed in the
lower part of the air quality distribution
and confidence in the magnitude and
significance of the associations begins to
decrease in the lower part of the air
quality distribution. Furthermore,
consistent with past reviews, there is no
single percentile value within a given
air quality distribution that is most
appropriate or ‘‘correct’’ to use to
characterize where our confidence in
associations becomes appreciably lower.
However, and as detailed further in the
PA, the range from the 25th to 10th
percentiles is a reasonable range to
consider as a region where there is
appreciably less confidence in the
associations observed in epidemiologic
studies compared to the means (U.S.
EPA, 2022b, p. 3–69).65
In evaluating the overall studyreported means, and concentrations
somewhat below the means from
epidemiologic studies, the PA focuses
on the form, averaging time and level of
the current primary annual PM2.5
standard. Consistent with the
approaches used in the 2012 and 2020
reviews (78 FR 3161–3162, January 15,
2013; 85 FR 82716–82717, December 18,
2020), the annual standard has been
utilized as the primary means of
providing public health protection
against the bulk of the distribution of
short- and long-term PM2.5 exposures.
Thus, the evaluation of the study65 As detailed in the 2011 PA, we note the
interrelatedness of the distributional statistics and
a range of one standard deviation around the mean
which represents approximately 68% of normally
distributed data, and in that one standard deviation
below the mean falls between the 25th and 10th
percentiles (U.S. EPA, 2011, p. 2–71; U.S. EPA,
2005, p. 5–22).
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reported mean concentrations from key
epidemiologic studies lends itself best
to evaluating the adequacy of the annual
PM2.5 standard (rather than the 24-hour
standard with its 98th percentile form).
This is true for the study-reported
means from both long-term and shortterm exposure epidemiologic studies,
recognizing that the overall mean PM2.5
concentrations reported in studies of
short-term (24-hour) exposures reflect
averages across the study population
and over the years of the study. Thus,
mean concentrations from short-term
exposure studies reflect long-term
averages of 24-hour PM2.5 exposure
estimates. In this manner, the
examination of study-reported means in
key epidemiologic studies in the PA
aims to evaluate the protection provided
by the annual PM2.5 standard against the
exposures where confidence is greatest
for associations with mortality and
morbidity. In addition, the protection
provided by the annual standard is
evaluated in conjunction with that
provided by the 24-hour standard, with
its 98th percentile form, which aims to
provide supplemental protection against
the short-term exposures to peak PM2.5
concentrations that can occur in areas
with strong contributions from local or
seasonal sources, even when overall
ambient mean PM2.5 concentrations in
an area remain relatively low.
In focusing on the annual standard,
and in evaluating the range of studyreported exposure concentrations for
which the strongest support for adverse
health effects exists, the PA examines
exposure concentrations in key
epidemiologic studies to determine
whether the current primary annual
PM2.5 standard provides adequate
protection against these exposure
concentrations. This means, as in past
reviews, application of a decision
framework based on assessing means
reported in key epidemiologic studies
must also consider how the study means
were computed and how these values
compare to the annual standard metric
(including the level, averaging time and
form) and the use of the monitor with
the highest PM2.5 design value in an area
for compliance. In the 2012 review, it
was recognized that the key
epidemiologic studies computed the
study mean using an average across
monitor-based PM2.5 concentrations. As
such, the Agency noted that this
decision framework applied an
approach of using maximum monitor
concentrations to determine compliance
with the standard, while selecting the
standard level based on consideration of
composite monitor concentrations.
Further, the Agency included analyses
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(Hassett-Sipple et al., 2010; Frank, 2012)
that examined the differences in these
two metrics (i.e., maximum monitor
concentrations and composite monitor
concentrations) across the U.S. and in
areas included in the key epidemiologic
studies and found that the maximum
design value in an area was generally
higher than the monitor average across
that area, with that amount varying
based on location and concentration.
This information was taken into account
in the Administrator’s final decision in
selecting a level for the primary annual
PM2.5 standard the 2012 review and
discussed more specifically in her
considerations on adequate margin of
safety.
Consistent with the approach taken in
2012, in assessing how the overall mean
(or median) PM2.5 concentrations
reported in key epidemiologic studies
can inform conclusions on the annual
primary PM2.5 standard, the PA notes
that the relationship between mean
PM2.5 concentrations and the area
design value continues to be an
important consideration in evaluating
the adequacy of the current or potential
alternative annual PM2.5 standard levels
in this reconsideration. In a given area,
the area design value is based on the
monitor in an area with the highest
PM2.5 concentrations and is used to
determine compliance with the
standard. The highest PM2.5
concentrations spatially distributed in
the area would generally occur at or
near the area design value monitor and
the distribution of PM2.5 concentrations
would generally be lower in other
locations and at monitors in that area.
As such, when an area is meeting a
specific annual standard level, the
annual average exposures in that area
are expected to be at concentrations
lower than that level and the average of
the annual average exposures across that
area are expected (i.e., a metric similar
to the study-reported mean values) to be
lower than that level.66
Another important consideration is
that there are a substantial number of
different types of epidemiologic studies
available since the 2012 review,
included in both the 2019 ISA and the
ISA Supplement, that make
understanding the relationship between
the mean PM2.5 concentrations and the
area design value even more important
66 In setting a standard level that would require
the design value monitor to meet a level equal to
the study-reported mean PM2.5 concentrations
would generally result in lower concentrations of
PM2.5 across the entire area, such that even those
people living near an area design value monitor
(where PM concentrations are generally highest)
will be exposed to PM2.5 concentrations below the
air quality conditions reported in the epidemiologic
studies.
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(U.S. EPA, 2019a; U.S. EPA, 2022a).
While the key epidemiologic studies in
the 2012 review were all monitor-based
studies, the newer studies include
hybrid modeling approaches, which
have emerged in the epidemiologic
literature as an alternative to approaches
that only use ground-based monitors to
estimate exposure. As assessed in the
2019 ISA and ISA Supplement, a
substantial number of epidemiologic
studies used hybrid model-based
methods in evaluating associations
between PM2.5 exposure and health
effects (U.S. EPA, 2019a; U.S. EPA,
2022a). Hybrid model-based studies
employ various fusion techniques that
combine ground-based monitored data
with air quality modeled estimates and/
or information from satellites to
estimate PM2.5 exposures.67
Additionally, hybrid modeling
approaches tend to broaden the areas
captured in the exposure assessment,
and in so doing, tend to report lower
mean PM2.5 concentrations than
monitor-based approaches because they
include more suburban and rural areas
where concentrations are lower. While
these studies provide a broader
estimation of PM2.5 exposures compared
to monitor-based studies (i.e., PM2.5
concentrations are estimated in areas
without monitors), the hybrid modeling
approaches result in study-reported
means that are more difficult to relate to
the annual standard metric and to the
use of maximum monitor design values
to assess compliance. In addition, to
further complicate the comparison,
when looking across these studies,
variations in how exposure is estimated
are present between such studies, which
affects how the study means are
calculated. Two important variations
across studies include: (1) variability in
spatial scale used (i.e., averages
computed across the nation (or large
portions of the country) versus a focus
on only CBSAs) and (2) variability in
exposure assignment methods (i.e.,
averaging across all grid cells [nonpopulation weighting], averaging across
a scaled-up area like a ZIP code [aspects
of population weighting applied], and/
or applying population weighting). To
elaborate further on the variability in
exposure assignment methods, studies
that use hybrid modeling approaches
can estimate PM2.5 concentrations at
different spatial resolutions, including
at 1 km x 1 km grid cells, at 12 km x
12 km grid cells, or at the census level
tract. Mean reported PM2.5
concentrations can then be estimated
67 More detailed information about hybrid model
methods and performance is described in section
2.3.3.2 of the PA (U.S. EPA, 2022b).
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either by averaging up to a larger spatial
resolution that corresponds to the
spatial resolution for which health data
exists (e.g., ZIP code level) and therefore
apply aspects of population weighting.
These values are then averaged across
all study locations at the larger spatial
resolution (e.g., averaged across all ZIP
codes in the study) over the study
period, resulting in the study-reported
mean 24-hour average or average annual
PM2.5 concentration. Other studies that
use hybrid modeling methods to
estimate PM2.5 concentrations may use
each grid cell to report the studyreported mean 24-hour average or
average annual PM2.5 concentration. As
such, these types of studies do not apply
population weighting in their mean
concentrations. In studies that use each
grid cell to report a mean PM2.5
concentration and do not apply aspects
of population weighting, the study mean
may not reflect the exposure
concentrations used in the
epidemiologic study to assess the
reported association. The impact of the
differences in methods is an important
consideration when comparing mean
concentrations across studies (U.S. EPA,
2022b, section 3.3.3.2.1). Thus, the PA
also considers the methods used to
estimate PM2.5 concentrations, which
vary from traditional methods using
monitoring data from ground-based
monitors 68 to those using more complex
hybrid modeling approaches.69
Given the emergence of the hybrid
model-based epidemiologic studies
since the 2012 review, the PA explores
the relationship between the approaches
used in these studies to estimate PM2.5
concentrations and the impact that the
different methods have on the studyreported mean PM2.5 concentrations.
The PA further seeks to understand how
the approaches and resulting mean
concentrations compare across studies,
as well as what the resulting mean
values represent relative to the annual
standard. In so doing, the PA presents
analyses that compare the area annual
design values, composite monitor PM2.5
68 In those studies that use ground-based monitors
alone to estimate long- or short-term PM2.5
concentrations, approaches include: (1) PM2.5
concentrations from a single monitor within a city/
county; (2) average of PM2.5 concentrations across
all monitors within a city/county or other defined
study area (e.g., CBSA); or (3) population-weighted
averages of exposures. Once the study location
average PM2.5 concentration is calculated, the
study-reported long-term average is derived by
averaging daily/annual PM2.5 concentrations across
all study locations over the entire study period.
69 Detailed information on the methods by which
mean PM2.5 concentrations are calculated in key
monitor- and hybrid model-based U.S. and
Canadian epidemiologic studies are presented in
Tables 3–6 through 3–9 in the PA (U.S. EPA,
2022b).
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concentrations, and mean
concentrations from two hybrid
modeling approaches, including
evaluation of the means when
population weighting is applied and
when population weighting is not
applied (U.S. EPA, 2022b, section
2.3.3.1). In the air quality analyses
comparing composite monitored PM2.5
concentrations with annual PM2.5 design
values in U.S. CBSAs, maximum annual
PM2.5 design values were approximately
10% to 20% higher than annual average
composite monitor concentrations (i.e.,
averaged across multiple monitors in
the same CBSA) (sections I.D.5.a above
and U.S. EPA, 2022b, section 2.3.3.1,
Figure 2–28 and Table 2–3). The
difference between the maximum
annual design value and average
concentration in an area can be smaller
or larger than this range (10–20%),
depending on a variety of factors such
as the number of monitors, monitor
siting characteristics, the distribution of
ambient PM2.5 concentrations, and how
the average concentrations are
calculated (i.e., averaged across
monitors versus across modeled grid
cells). Results of this analysis suggest
that there will be a distribution of
concentrations and the maximum
annual average monitored concentration
in an area (at the design value monitor,
used for compliance with the standard),
will generally be 10–20% higher than
the average PM2.5 concentration across
the other monitors in the area. Thus, in
considering how the annual standard
levels would relate to the study-reported
means from key monitor-based
epidemiologic studies, the PA generally
concludes that an annual standard level
that is no more than 10–20% higher
than monitor-based study-reported
mean PM2.5 concentrations would
generally maintain air quality exposures
to be below those associated with the
study-reported mean PM2.5
concentrations, exposures for which the
strongest support for adverse health
effects occurring is available.
The PA also evaluates data from two
hybrid modeling approaches (DI2019
and HA2020) that have been used in
several recent epidemiologic studies
(U.S. EPA, 2022b, section 2.3.3.2.4).70
The analysis shows that the means vary
when PM2.5 concentrations are
estimated in urban areas only (CBSAs)
versus when the averages were
calculated with all or most grid cells
nationwide, likely because areas
included outside of CBSAs tend to be
more rural and have lower estimated
70 More details on the evaluation of the two
hybrid modeling approaches is provided in section
2.3.3.2.4 of the PA (U.S. EPA, 2022b).
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PM2.5 concentrations. The PA
recognizes the importance of this
variability in the means since the study
areas included in the calculation of the
mean, and more specifically whether a
study is focused on nationwide,
regional, or urban areas, will affect the
calculation of the study mean based on
how many rural areas are included with
lower estimated PM2.5 concentrations.
While the determination of what spatial
scale to use to estimate PM2.5
concentrations does not inherently
affect the quality of the epidemiologic
study, the spatial scale can influence the
calculated long-term mean
concentration across the study area and
period. The results of the analysis show
that, regardless of the hybrid modeling
approach assessed, the annual average
PM2.5 concentrations in CBSA-only
analyses are 4–8% higher than for
nationwide analyses, likely as a result of
higher PM2.5 concentrations in more
densely populated areas, and exclusion
of more rural areas (U.S. EPA, 2022b,
Table 2–4). When evaluating
comparisons between surfaces that
estimate exposure using population
weighting versus surfaces that do not
calculate means using population
weighting, surfaces that calculate longterm mean PM2.5 concentrations with
population-weighted averages have
higher average annual PM2.5
concentrations, compared to annual
PM2.5 concentrations in analyses that do
not apply population weighting.71
Analyses show that average maximum
annual design values are 40 to 50%
higher when compared to annual
average PM2.5 concentrations estimated
without population weighting and are
15% to 18% higher when compared to
average annual PM2.5 concentrations
with population weighting applied
(similar to the differences observed for
the composite monitor comparison
values for the monitor-based
epidemiologic studies) (U.S. EPA,
2022b, section 2.3.3.2.4). Given these
results, it is worth noting that for the
studies using the hybrid modeling
approaches, the choice of methodology
employed in calculating the studyreported means (i.e., using population
weighting or not), and not a difference
in estimates of exposure in the study
itself, can produce substantially
different study-reported mean values,
with the approach that does not utilize
71 The annual PM
2.5 concentrations for the
population-weighted averages ranged from 8.2–10.2
mg/m3, while those that do not apply population
weighting ranged from 7.0–8.6 mg/m3. Average
maximum annual design values ranged from 9.5 to
11.7 mg/m3.
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population weighting producing a much
lower value.
Based on these results, and similar to
conclusions for the monitor-based
studies, the PA generally concludes that
study-reported mean concentrations in
the studies that employ hybrid
modeling approaches and populationweight the mean are associated with air
quality conditions that would be
achieved by meeting annual standard
levels that are 15–18% higher than
study-reported means. Therefore, an
annual standard level that is no more
than 15–18% higher than the studyreported means would generally
maintain air quality exposures to be
below those associated with the studyreported mean PM2.5 concentrations,
exposures for which we have the
strongest support for adverse health
effects occurring. For the studies that
utilize hybrid modeling approaches but
do not incorporate population weighting
in calculating the mean, the annual
design values associated with these air
quality conditions are expected to be
much higher (i.e., 40–50% higher) and
this larger difference makes it more
difficult to consider how these studies
can be used to determine the adequacy
of the protection afforded by the current
or potential alternative annual
standards. Additionally, as noted above
in studies that utilize hybrid modeling
approaches and that do not incorporate
population weighting in calculating the
mean (e.g., use each grid cell to
calculate a mean PM2.5 concentration),
the study mean does not reflect the
exposure concentrations used in the
epidemiologic study to assess the
reported association.
The PA notes that while these
analyses can be useful to informing the
understanding of the relationship
between study-reported mean
concentrations and the level of the
annual standard, some limitations of
this assessment of the information must
be recognized (U.S. EPA, 2022a, section
3.3.3.2.1). First, the comparisons used
only two hybrid modeling approaches.
Although the two hybrid modeling
surfaces have been used in a number of
recent epidemiologic studies, they
represent just two of the many hybrid
modeling approaches that have been
used in epidemiologic studies to
estimate PM2.5 concentrations. These
methods continue to evolve over time,
with further development and
improvement to prediction models that
estimate PM2.5 concentrations in
epidemiologic studies. In addition to
differences in hybrid modeling
approaches, epidemiologic studies also
use different methods to assign a
population-weighted average PM2.5
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concentration to their study population,
and the assessment presented in the PA
does not evaluate all of the potential
methods that could be used.
Additionally, while some of these
epidemiologic studies also provide
information on the broader distributions
of exposure estimates and/or health
events and the PM2.5 concentrations
corresponding to the lower percentiles
of those data (e.g., 25th and/or 10th), the
air quality analysis in the PA focuses on
mean PM2.5 concentrations and a similar
comparison for these lower percentiles
was not assessed. Therefore, any direct
comparison of study-reported PM2.5
concentrations corresponding to lower
percentiles and annual design values is
more uncertain than such comparisons
with the mean. Finally, air quality
analysis presented in the PA and
detailed above in section I.D.5 included
two hybrid modeling-based approaches
that used U.S.-based air quality
information for estimating PM2.5
concentrations. As such, the analyses
are most relevant to interpreting the
study-reported mean concentrations
from U.S. epidemiologic studies and do
not provide additional information
about how the mean exposures
concentrations reported in
epidemiologic studies in other countries
would compare to annual design values
observed in the U.S. In addition, while
information from Canadian studies can
be useful in assessing the adequacy of
the annual standard, differences in the
exposure environments and population
characteristics between the U.S. and
other countries can affect the studyreported mean value and its relationship
with the annual standard level. Sources
and pollutant mixtures, as well as PM2.5
concentration gradients, may be
different between countries, and the
exposure environments in other
countries may differ from those
observed in the U.S. Furthermore,
differences in population characteristics
and population densities can also make
it challenging to directly compare
studies from countries outside of the
U.S. to a design value in the U.S.
As with the experimental studies
discussed above, the PA focuses on
epidemiologic studies assessed in the
2019 ISA and ISA Supplement that have
the potential to be most informative in
reaching decisions on the adequacy of
the primary PM2.5 standards. The PA
focuses on epidemiologic studies that
provide strong support for ‘‘causal’’ or
‘‘likely to be causal’’ relationships with
PM2.5 exposures in the 2019 ISA.
Further, the PA also focuses on the
health effect associations that are
determined in the 2019 ISA and ISA
Supplement to be consistent across
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studies, coherent with the broader body
of evidence (e.g., including animal and
controlled human exposure studies),
and robust to potential confounding by
co-occurring pollutants and other
factors.72 In particular the PA considers
the U.S. and Canadian epidemiologic
studies to be more useful for reaching
conclusions on the current standards
than studies conducted in other
countries, given that the results of the
U.S. and Canadian studies are more
directly applicable for quantitative
considerations, whereas studies
conducted in other countries reflect
different populations, exposure
characteristics, and air pollution
mixtures. Additionally, epidemiologic
studies outside of the U.S. and Canada
generally reflect higher PM2.5
concentrations in ambient air than are
currently found in the U.S., and are less
relevant to informing questions about
adequacy of the current standards.73
However, and as noted above, the PA
also recognizes that while information
from Canadian studies can be useful in
assessing the adequacy of the annual
standard, there are still important
differences between the exposure
environments in the U.S. and Canada
and interpreting the data (e.g., mean
concentrations) from the Canadian
studies in the context of a U.S.-based
standard may present challenges in
72 As described in the Preamble to the ISAs (U.S.
EPA, 2015), ‘‘the U.S. EPA emphasizes the
importance of examining the pattern of results
across various studies and does not focus solely on
statistical significance or the magnitude of the
direction of the association as criteria of study
reliability. Statistical significance is influenced by
a variety of factors including, but not limited to, the
size of the study, exposure and outcome
measurement error, and statistical model
specifications. Statistical significance may be
informative; however, it is just one of the means of
evaluating confidence in the observed relationship
and assessing the probability of chance as an
explanation. Other indicators of reliability such as
the consistency and coherence of a body of studies
as well as other confirming data may be used to
justify reliance on the results of a body of
epidemiologic studies, even if results in individual
studies lack statistical significance. Traditionally,
statistical significance is used to a larger extent to
evaluate the findings of controlled human exposure
and animal toxicological studies. Understanding
that statistical inferences may result in both false
positives and false negatives, consideration is given
to both trends in data and reproducibility of results.
Thus, in drawing judgments regarding causality, the
U.S. EPA emphasizes statistically significant
findings from experimental studies, but does not
limit its focus or consideration to statistically
significant results in epidemiologic studies.’’
73 This emphasis on studies conducted in the U.S.
or Canada is consistent with the approach in the
2012 and 2020 reviews of the PM NAAQS (U.S.
EPA, 2011, section 2.1.3; U.S. EPA, 2020a, section
3.2.3.2.1) and with approaches taken in other
NAAQS reviews. However, the importance of
studies in the U.S., Canada, and other countries in
informing an ISA’s considerations of the weight of
the evidence that informs causality determinations
is recognized.
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directly and quantitatively informing
questions regarding the adequacy of the
current or potential alternative the
levels of the annual standard. Lastly, the
PA emphasizes multicity/multistate
studies that examine health effect
associations, as such studies are more
encompassing of the diverse
atmospheric conditions and population
demographics in the U.S. than studies
that focus on a single city or state.
Figures 3–4 through 3–7 in the PA
summarize the study details for the key
U.S. and Canadian epidemiologic
studies (U.S. EPA, 2022b, section
3.3.3.2.1).74
The key epidemiologic studies
identified in the PA indicate generally
positive and statistically significant
associations between estimated PM2.5
exposures (short- or long-term) and
mortality or morbidity across a range of
ambient PM2.5 concentrations (U.S.
EPA, 2022b, section 3.3.3.2.1), report
overall mean (or median) PM2.5
concentrations, and include those for
which the years of PM2.5 air quality data
used to estimate exposures overlap
entirely with the years during which
health events are reported.75
Additionally, for studies that estimate
PM2.5 exposure using hybrid modeling
approaches, the PA also considers the
approach used to estimate PM2.5
concentrations and the approach used to
validate hybrid model predictions when
determining those studies considered as
key epidemiologic studies 76 and
focuses on those studies that use recent
methods based on surfaces with fused
74 The cohorts examined in the studies included
in Figure 3–4 to Figure 3–7 of the PA include large
numbers of individuals in the general population,
and often also include those populations identified
as at-risk (i.e., children, older adults, minority
populations, and individuals with pre-existing
cardiovascular and respiratory disease).
75 For some studies of long-term PM
2.5 exposures,
exposure is estimated from air quality data
corresponding to only part of the study period,
often including only the later years of the health
data, and are not likely to reflect the full ranges of
ambient PM2.5 concentrations that contributed to
reported associations. While this approach can be
reasonable in the context of an epidemiologic study
that is evaluating health effect associations with
long-term PM2.5 exposures, under the assumption
that spatial patterns in PM2.5 concentrations are not
appreciably different during time periods for which
air quality information is not available (e.g., Chen
et al., 2016), the PA focuses on the distribution of
ambient PM2.5 concentrations that could have
contributed to reported health outcomes. Therefore,
the PA identifies studies as key epidemiologic
studies when the years of air quality data and
health data overlap in their entirety.
76 Such studies are identified as those that use
hybrid modeling approaches for which recent
methods and models were used (e.g., recent
versions and configurations of the air quality
models); studies that are fused with PM2.5 data from
national monitoring networks (i.e., FRM/FEM data);
and studies that reported a thorough model
performance evaluation for core years of the study.
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with monitored PM2.5 concentration
data (U.S. EPA, 2022b, section
3.3.3.2.1).
Figure 1 below (U.S. EPA, 2022b,
Figure 3–8) highlights the overall mean
(or median) PM2.5 concentrations
reported in key U.S. studies that use
ground-based monitors alone to estimate
long- or short-term PM2.5 exposure.77
For the small subset of studies with
available information on the broader
distributions of underlying data, Figure
1 below also identifies the study-period
mean PM2.5 concentrations
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77 Canadian studies that use ground-based
monitors estimate long- or short-term PM2.5
exposures are found in Figure 3–9 of the PA,
including concentrations corresponding to the 25th
and 10th percentiles of estimated exposures or
health events, when available (U.S. EPA, 2022b).
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corresponding to the 25th and 10th
percentiles of health events78 (see
Appendix B, Section B.2 of the PA for
more information). Figure 2 (U.S. EPA,
2022a, Figure 3–14) presents overall
means of predicted PM2.5 concentrations
for key U.S. model-based epidemiologic
studies that apply aspects of populationweighting, and the concentrations
corresponding to the 25th and 10th
percentiles of estimated exposures or
health events79 when available (see
78 That is, 25% of the total health events occurred
in study locations with mean PM2.5 concentrations
(i.e., averaged over the study period) below the 25th
percentiles identified in Figure 3–8 of the PA and
10% of the total health events occurred in study
locations with mean PM2.5 concentrations below the
10th percentiles identified.
79 For most studies in Figure 2 below (Figure 3–
14 in the PA), 25th percentiles of exposure
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Appendix B, section B.3 for additional
information).80
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estimates are presented. The exception is Di et al.
(2017b), for which Figure 2 (U.S. EPA, 2022b,
Figure 3–14) presents the short-term PM2.5 exposure
estimates corresponding to the 25th and 10th
percentiles of deaths in the study population (i.e.,
25% and 10% of deaths occurred at concentrations
below these concentrations). In addition, the
authors of Di et al. (2017b) provided populationweighted exposure values. The 10th and 25th
percentiles of these population-weighted exposure
estimates are 7.9 and 9.5 mg/m3, respectively.
80 Overall mean (or median) PM
2.5 concentrations
reported in key Canadian studies that use modelbased approaches to estimate long- or short-term
PM2.5 concentrations and the concentrations
corresponding to the 25th and 10th percentiles of
estimated exposures or health events, when
available are found in Figure 3–9 of the PA (U.S.
EPA, 2022b).
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Figure 2. Hybrid model-predicted PM2.s concentrations in key U.S. epidemiologic studies that apply aspects of population-weighting.
(Asterisks denote studies included in the ISA Supplement)
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Based on its evaluation of studyreported mean concentrations, the PA
notes that key epidemiologic studies
conducted in the U.S. or Canada report
generally positive and statistically
significant associations between
estimated PM2.5 exposures (short- or
long-term) and mortality or morbidity
across a wide range of ambient PM2.5
concentrations (U.S. EPA, 2022b,
section 3.3.3.2.1). The PA makes a
number of observations with regard to
the study-reported PM2.5 concentrations
in the key U.S. and Canadian
epidemiologic studies.
The PA first considers the PM2.5
concentrations from the key U.S.
epidemiologic studies. For studies that
use monitors to estimate PM2.5
exposures, overall mean PM2.5
concentrations range between 9.9 mg/
m3 81 to 16.5 mg/m3 (Figure 1 and U.S.
EPA, 2022b, Figure 3–8). For key U.S.
epidemiologic studies that use hybrid
model-predicted exposures and apply
aspects of population-weighting, mean
PM2.5 concentrations range from 9.3 mg/
m3 to just above 12.2 mg/m3 (Figure 2
and U.S. EPA, 2022b, Figure 3–14). In
studies that average up from the grid
cell level to the ZIP code, postal code,
or census tract level, mean PM2.5
concentrations range from 9.8 mg/m3 to
12.2 mg/m3. In the one study that
population-weighted the grid cell prior
to averaging up to the ZIP code or
census tract level report mean PM2.5
concentrations of 9.3 mg/m3. Based on
air quality analyses noted above, these
hybrid modelled epidemiologic studies
are expected to report means similar to
those from monitor-based studies.
Other key U.S. epidemiologic studies
that use hybrid modeling approaches
estimate mean PM2.5 exposure by
averaging from the grid cell spatial
resolution across the entire study area,
whether that be the nation or a region
of the country. These studies do not
weight the estimated exposure
concentrations based on population
density or location of health events.
Additionally, the study mean reported
in these studies may not reflect the
exposure concentrations used in the
epidemiologic study to assess the
reported association. Because of this,
these reported mean concentrations are
the most different (and much lower)
than the means reported in monitorbased studies. Due to the methodology
employed in calculating the studyreported means and not necessarily a
81 This
is generally consistent with, but slightly
below, the lowest study-reported mean PM2.5
concentration from monitor-based studies available
in the 2020 PA, which was 10.7 mg/m3 (U.S. EPA,
2020a, Figure 3–7).
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difference in estimates of exposure,
these epidemiologic studies are
expected to report some of the lowest
mean values. For these studies, the
reported mean PM2.5 concentrations
range from 8.1 mg/m3 to 11.9 mg/m3 (U.S.
EPA, 2022b, Figure 3–14). As noted
above, for studies that utilize hybrid
modeling approaches but do not
incorporate population weighting in
calculating the mean, the associated
annual design values would be expected
to be much higher (i.e., 40–50% higher)
than the study-reported means. This
larger difference between design values
and study-reported mean concentrations
makes it more difficult to consider how
these studies can be used to determine
the adequacy of the protection afforded
by the current or potential alternative
annual standards (U.S. EPA, 2022b,
section 3.3.3.2.1).
In addition to the mean PM2.5
concentrations, a subset of the key U.S.
epidemiologic studies report PM2.5
concentrations corresponding to the
25th and 10th percentiles of health data
or exposure estimates to provide insight
into the concentrations that comprise
the lower quartiles of the air quality
distributions. In studies that use
monitors to estimate PM2.5 exposures,
25th percentiles of health events
correspond to PM2.5 concentrations (i.e.,
averaged over the study period for each
study city) at or above 11.5 mg/m3 and
10th percentiles of health events
correspond to PM2.5 concentrations at or
above 9.8 mg/m3 (i.e., 25% and 10% of
health events, respectively, occur in
study locations with PM2.5
concentrations below these values)
(Figure 1 and U.S. EPA, 2022b, Figure
3–8). Of the key U.S. epidemiologic
studies that use hybrid modeling
approaches and population-weighting to
estimate long-term PM2.5 exposures, the
ambient PM2.5 concentrations
corresponding to 25th percentiles of
estimated exposures are 9.1 mg/m3
(Figure 2 and U.S. EPA, 2022b, Figure
3–14). In key U.S. epidemiologic studies
that use hybrid modeling approaches
and apply population-weighting to
estimate short-term PM2.5 exposures, the
ambient concentrations corresponding
to 25th percentiles of estimated
exposures, or health events, are 6.7 mg/
m3 (Figure 2 and U.S. EPA, 2022b,
Figure 3–14). In key U.S. epidemiologic
studies that use hybrid modeling
approaches and do not apply
population-weighting to estimate PM2.5
exposures, the ambient concentrations
corresponding to 25th percentiles of
estimated exposures, or health events,
range from 4.6 to 9.2 mg/m3 (U.S. EPA,
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2022b, Figure 3–14).82 In the key
epidemiologic studies that apply hybrid
modeling approaches with populationweighting and with information
available on the 10th percentile of
health events, the ambient PM2.5
concentration corresponding to that
10th percentile range from 4.7 mg/m3 to
7.3 mg/m3 (Figure 2 and U.S. EPA,
2022b, Figure 3–14).
The PA next considers the PM2.5
concentrations from the key Canadian
epidemiologic studies. Generally, the
study-reported mean concentrations in
Canadian studies are lower than those
reported in the U.S. studies for both
monitor-based and hybrid model
methods. For the majority of key
Canadian epidemiologic studies that use
monitor-based exposure, mean PM2.5
concentrations generally ranged from
7.0 mg/m3 to 9.0 mg/m3 (U.S. EPA,
2022b, Figure 3–9). For these studies,
25th percentiles of health events
correspond to PM2.5 concentrations at or
above 6.5 mg/m3 and 10th percentiles of
health events correspond to PM2.5
concentrations at or above 6.4 mg/m3
(U.S. EPA, 2022b, Figure 3–9). For the
key Canadian epidemiologic studies that
use hybrid model-predicted exposure,
the mean PM2.5 concentrations are
generally lower than in U.S. modelbased studies (U.S. EPA, 2022b, Figure
3–10), ranging from approximately 6.0
mg/m3 to just below 10.0 mg/m3 (U.S.
EPA, 2022b, Figure 3–11). The majority
of the key Canadian epidemiologic
studies that used hybrid modeling were
completed at the nationwide scale,
while four studies were completed at
the regional geographic spatial scale. In
addition, all the key Canadian
epidemiologic studies apply aspects of
population weighting, where all grid
cells within a postal code are averaged,
individuals are assigned exposure at the
postal code resolution, and study mean
PM2.5 concentrations are based on the
average of individual exposures. The
majority of studies estimating exposure
nationwide range between just below
6.0 mg/m3 to 8.0 mg/m3 (U.S. EPA,
2022b, Figure 3–11). One study by
Erickson et al. (2020) presents an
analysis related immigrant status and
length of residence in Canada versus
non-immigrant populations, which
accounts for the four highest mean PM2.5
concentrations which range between 9.0
mg/m3 and 10.0 mg/m3 (U.S. EPA, 2022b,
Figure 3–11). The four studies that
estimate exposure at the regional scale
82 As noted above, in this study (Shi et al., 2016),
the authors report that most deaths occurred at or
above the 75th percentile of annual exposure
estimates (i.e., 10 mg/m3). The short-term exposure
estimates accounting for most deaths are not
presented in the published study.
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report mean PM2.5 concentrations that
range from 7.8 mg/m3 to 9.8 mg/m3 (U.S.
EPA, 2022b, Figure 3–11). Three key
Canadian epidemiologic studies report
information on the 25th percentile of
health events. In these studies, the
ambient PM2.5 concentration
corresponding to the 25th percentile is
approximately 8.0 mg/m3 in two studies,
and 4.3 mg/m3 in a third study (U.S.
EPA, 2022b, Figure 3–11).
In addition to the expanded body of
evidence from the key U.S.
epidemiologic studies discussed above,
there are also a subset of epidemiologic
studies that have emerged that further
inform an understanding of the
relationship between PM2.5 exposure
and health effects, including studies
with the highest exposures excluded
(restricted analyses), epidemiologic
studies that employed statistical
approaches that attempt to more
extensively account for confounders and
are more robust to model
misspecification (i.e., used alternative
methods for confounder control),83 and
accountability studies (U.S. EPA, 2019a,
U.S. EPA, 2021a, U.S. EPA, 2022b).
Restricted analyses are studies that
examine health effect associations in
analyses with the highest exposures
excluded, restricting analyses to daily
exposures less than the 24-hour primary
PM2.5 standard and annual exposures
less than the annual PM2.5 standard. The
PA presents a summary of restricted
analyses evaluated in the 2019 ISA and
ISA Supplement (U.S. EPA, 2022b,
Table 3–10). The restricted analyses can
be informative in assessing the nature of
the association between long-term
exposures (e.g., annual average
concentrations <12.0 mg/m3) or shortterm exposures (e.g., daily
concentrations <35 mg/m3) when
looking only at exposures to lower
concentrations, including whether the
association persists in such restricted
analyses compared to the same analyses
for all exposures, as well as whether the
association is stronger, in terms of
magnitude and precision, than when
completing the same analysis for all
exposures. While these studies are
useful in supporting the confidence and
83 As noted in the ISA Supplement (U.S. EPA,
2022a, p. 1–3): ‘‘In the peer-reviewed literature,
these epidemiologic studies are often referred to as
alternative methods for confounder control. For the
purposes of this Supplement, this terminology is
not used to prevent confusion with the main
scientific conclusions (i.e., the causality
determinations) presented within an ISA. In
addition, as is consistent with the weight-ofevidence framework used within ISAs and
discussed in the Preamble to the Integrated Science
Assessments, an individual study on its own cannot
inform causality, but instead represents a piece of
the overall body of evidence.’’
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strength of associations at lower
concentrations, these studies also have
inherent uncertainties and limitations,
including uncertainty in how studies
exclude concentrations (e.g., are they
excluded at the modeled grid cell level,
the ZIP code level) and in how
concentrations in studies that restrict air
quality data relate to design values for
the annual and 24-hour standards.
Further, these studies often do not
report descriptive statistics (e.g., mean
PM2.5 concentrations, or concentrations
at other percentiles) that allow for
additional consideration of this
information. As such, while these
studies can provide additional
supporting evidence for associations at
lower concentrations, the PA notes that
there are also limitations in how to
interpret these studies when evaluating
the adequacy of the current or potential
alternative standards. Restricted
analyses provide additional information
on the nature of the association between
long- or short-term exposures when
analyses are restricted to lower PM2.5
concentrations. Further, these studies
indicate that effect estimates are
generally greater in magnitude in the
restricted analyses for long- and shortterm PM2.5 exposure compared to the
main analyses.
In two U.S. studies that report mean
PM2.5 concentrations in restricted
analyses and that estimate effects
associated with long-term exposure to
PM2.5, the effect estimates are greater in
the restricted analyses than in the main
analyses. Di et al. (2017a) and Dominici
et al. (2019) report positive and
statistically significant associations in
analyses restricted to concentrations
less than 12.0 mg/m3 for all-cause
mortality and effect estimates are greater
in the restricted analyses than effect
estimates reported in main analyses. In
addition, both studies report mean PM2.5
concentrations of 9.6 mg/m3. While none
of the U.S. studies of short-term
exposure present mean PM2.5
concentrations for the restricted
analyses, these studies generally have
mean 24-hour average PM2.5
concentrations in the main analyses
below 12.0 mg/m3, and report increases
in the effect estimates in the restricted
analyses compared to the main analyses.
Additionally, in the one Canadian study
of long-term PM2.5 exposure, Zhang et
al. (2021) conducted analyses where
annual PM2.5 concentrations were
restricted to concentrations below 10.0
mg/m3 and 8.8 mg/m3, which presumably
have lower mean concentrations than
the mean of 7.8 mg/m3 reported in the
main analyses, though restricted
analysis mean PM2.5 concentrations are
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not reported. Effect estimates for nonaccidental mortality are greater in
analyses restricted to PM2.5
concentrations less than 10.0 mg/m3, but
less in analyses restricted to <8.8 mg/m3.
The second type of studies that have
recently emerged and further inform the
consideration of the relationship
between PM2.5 exposure and health
effects in the PA are those that employ
alternative methods for confounder
control. Alternative methods for
confounder control seek to mimic
randomized experiments through the
use of study design and statistical
methods to more extensively account for
confounders and are more robust to
model misspecification. The PA
presents a summary of the studies that
employ alternative methods for
confounder control, and employ a
variety of statistical methods, which are
evaluated in the 2019 ISA and ISA
Supplement (U.S. EPA, 2022b, Table 3–
11). These studies reported consistent
results among large study populations
across the U.S. and can further inform
the relationship between long- and
short-term PM2.5 exposure and total
mortality. Studies that employ
alternative methods for confounder
control to assess the association
between long-term exposure to PM2.5
and mortality provide additional
support for the associations reported in
the broader body of cohort studies that
examined long-term PM2.5 exposure and
mortality.
Lastly, there is a subset of
epidemiologic studies that assess
whether long-term reductions in
ambient PM2.5 concentrations result in
corresponding reductions in health
outcomes. These include studies that
evaluate the potential for improvements
in public health, including reductions
in mortality rates, increases in life
expectancy, and reductions in
respiratory disease as ambient PM2.5
concentrations have declined over time.
Some of these studies, accountability
analyses, provide insight on whether the
implementation of environmental
policies or air quality interventions
result in changes/reductions in air
pollution concentrations and the
corresponding effect on health
outcomes.84 The PA presents a
summary of these studies, which are
assessed in the 2019 ISA and ISA
Supplement (U.S. EPA, 2022b, Table 3–
12). These studies lend support for the
conclusion that improvements in air
84 Given the nature of these studies, the majority
tend to focus on time periods in the past during
which ambient PM2.5 concentrations were
substantially higher than those measured more
recently (e.g., see U.S. EPA, 2022b, Figure 2–16).
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quality are associated with
improvements in public health.
More specifically, of the
accountability studies that account for
changes in PM2.5 concentrations due to
a policy or the implementation of an
intervention to assess whether there was
evidence of changes in associations with
mortality or cardiovascular effects due
to changes in annual PM2.5
concentrations, Corrigan et al. (2018),
Henneman et al. (2019b), and Sanders et
al. (2020a) present analyses with
starting concentrations (or
concentrations prior to the policy or
intervention) below 12.0 mg/m3.
Henneman et al. (2019b) explored the
changes in modeled PM2.5
concentrations following the retirement
of coal fired power plants in the U.S.,
and found that reductions from mean
annual PM2.5 concentrations of 10.0 mg/
m3 in 2005 to mean annual PM2.5
concentrations of 7.2 mg/m3 in 2012
from coal-fueled power plants resulted
in corresponding reductions in the
number of cardiovascular-related
hospital admissions, including for all
cardiovascular disease, acute MI, stroke,
heart failure, and ischemic heart disease
in those aged 65 and older. Corrigan et
al. (2018) examined whether there was
a change in the cardiovascular mortality
rate before (2000–2004) and after (2005–
2010) implementation of the first annual
PM2.5 NAAQS implementation based on
mortality data from the National Center
for Health Statistics and reported 1.10
(95% confidence interval (CI): 0.37,
1.82) fewer cardiovascular deaths per
year per 100,000 people for each 1 mg/
m3 reduction in annual PM2.5
concentrations. When comparing
whether counties met the annual PM2.5
standard (attainment counties), there
were 1.96 (95% CI: 0.77, 3.15) fewer
cardiovascular deaths for each 1 mg/m3
reduction in annual PM2.5
concentrations between the two periods
for attainment counties, whereas for
non-attainment counties (e.g., counties
that did not meet the annual PM2.5
standard), there were 0.59 (95% CI:
¥0.54, 1.71) fewer cardiovascular
deaths between the two periods. And
lastly, Sanders et al. (2020a) examined
whether policy actions (i.e., the first
annual PM2.5 NAAQS implementation
rule in 2005 for the 1997 annual PM2.5
standard with a 3-year annual average of
15 mg/m3) reduced PM2.5 concentrations
and mortality rates in Medicare
beneficiaries between 2000–2013. They
report evidence of changes in
associations with mortality (a decreased
mortality rate of ∼0.5 per 1,000 in
attainment and non-attainment areas)
due to changes in annual PM2.5
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concentrations in both attainment and
non-attainment areas. Additionally,
attainment areas had starting
concentrations below 12.0 mg/m3 prior
to implementation of the annual PM2.5
NAAQS in 2005. In addition, following
implementation of the annual PM2.5
NAAQS, annual PM2.5 concentrations
decreased by 1.59 mg/m3 (95% CI: 1.39,
1.80) which corresponded to a reduction
in mortality rates among individuals 65
years and older (0.93% [95% CI: 0.10%,
1.77%]) in non-attainment counties
relative to attainment counties. In a life
expectancy study, Bennett et al. (2019)
reports increases in life expectancy in
all but 14 counties (1325 of 1339
counties) that have exhibited reductions
in PM2.5 concentrations from 1999 to
2015. These studies provide support for
improvements in public health
following the implementation of
policies, including in areas with PM2.5
concentrations below the level of the
current annual standard, as well as
increases in life expectancy in areas
with reductions in PM2.5 concentrations.
4. Uncertainties in the Health Effects
Evidence
The PA recognizes that there are a
number of uncertainties and limitations
associated with the available health
effects evidence. Although the
epidemiologic studies clearly
demonstrate associations between longand short-term PM2.5 exposures and
health outcomes, several uncertainties
and limitations in the health effects
evidence remain. Epidemiologic studies
evaluating short-term PM2.5 exposure
and health effects have reported
heterogeneity in associations between
cities and geographic regions within the
U.S. Heterogeneity in the associations
observed across epidemiologic studies
may be due in part to exposure error
related to measurement-related issues,
the use of central fixed-site monitors to
represent population exposure to PM2.5,
and a limited understanding of factors
including exposure error related to
measurement-related issues, variability
in PM2.5 composition regionally, and
factors that result in differential
exposures (e.g., topography, the built
environment, housing characteristics,
personal activity patterns).
Heterogeneity is expected when the
methods or the underlying distribution
of covariates vary across studies (U.S.
EPA, 2019a, p. 6–221). Studies assessed
in the 2019 ISA and ISA Supplement
have advanced the state of exposure
science by presenting innovative
methodologies to estimate PM exposure,
detailing new and existing measurement
and modeling methods, and further
informing our understanding of the
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influence of exposure measurement
error due to exposure estimation
methods on the associations between
PM2.5 and health effects reported in
epidemiologic studies (U.S. EPA, 2019a,
section 1.2.2; U.S. EPA, 2022a). Data
from PM2.5 monitors continue to be
commonly used in health studies as a
surrogate for PM2.5 exposure, and often
provide a reasonable representation of
exposures throughout a study area (U.S.
EPA, 2019a, section 3.4.2.2; U.S. EPA,
2022a, section 3.2.2.2.2). However, an
increasing number of studies employ
hybrid modeling methods to estimate
PM2.5 exposure using data from several
sources, often including satellites and
models, in addition to ground-based
monitors. These hybrid models typically
have good cross-validation, especially
for PM2.5, and have the potential to
reduce exposure measurement error and
uncertainty in the health effect
estimates from epidemiologic models of
long-term exposure (U.S. EPA, 2019a,
section 3.5; U.S. EPA, 2022a, section
2.3.3).
While studies using hybrid modeling
methods have reduced exposure
measurement error and uncertainty in
the health effect estimates, these studies
use a variety of approaches to estimate
PM2.5 concentrations and to assign
exposure to assess the association
between health outcomes and PM2.5
exposure. This variability in
methodology has inherent limitations
and uncertainties, as described in more
detail in section 2.3.3.1.5 of the PA, and
the performance of the modeling
approaches depends on the availability
of monitoring data which varies by
location. Factors that likely contribute
to poorer model performance often
coincide with relatively low ambient
PM2.5 concentrations, in areas where
predicted exposures are at a greater
distance to monitors, and under
conditions where the reliability and
availability of key datasets (e.g., air
quality modeling) are limited. Thus,
uncertainty in hybrid model predictions
becomes an increasingly important
consideration as lower predicted
concentrations are considered.
Regardless of whether a study uses
monitoring data or a hybrid modeling
approach when estimating PM2.5
exposures, one key limitation that
persists is associated with the
interpretation of the study-reported
mean PM2.5 concentrations and how
they compare to design values, the
metric that describe the air quality
status of a given area relative to the
NAAQS.85 As discussed above in
85 For the annual PM
2.5 standard, design values
are calculated as the annual arithmetic mean PM2.5
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section II.B.3.b, the overall mean PM2.5
concentrations reported by key
epidemiologic studies reflect averaging
of short- or long-term PM2.5 exposure
estimates across location (i.e., across
multiple monitors or across modeled
grid cells) and over time (i.e., over
several years). For monitor-based
studies, the comparison is somewhat
more straightforward than for studies
that use hybrid modeling methods, as
the monitors used to estimate exposure
in the epidemiologic studies are
generally the same monitors that are
used to calculate design values for a
given area. It is expected that areas
meeting a PM2.5 standard with a
particular level would be expected to
have average PM2.5 concentrations (i.e.,
averaged across space and over time in
the area) somewhat below that standard
level., but the difference between the
maximum annual design value and
average concentration in an area can be
smaller or larger than analyses
presented above in section I.D.5.a, likely
depending on factors such as the
number of monitors, monitor siting
characteristics, and the distribution of
ambient PM2.5 concentrations. For
studies that use hybrid modeling
methods to estimate PM2.5
concentrations, the comparison between
study-reported mean PM2.5
concentrations and design values is
more complicated given the variability
in the modeling methods, temporal
scales (i.e., daily versus annual), and
spatial scales (i.e., nationwide versus
urban) across studies. Analyses above in
section I.D.5.b and detailed more in the
PA (U.S. EPA, 2022b, section 2.3.3.2.4)
present a comparison between two
hybrid modeling surfaces, which
explored the impact of these factors on
the resulting mean PM2.5 concentrations
and provided additional information
about the relationship between mean
concentrations from studies using
hybrid modeling methods and design
values. However, the results of those
analyses only reflect two surfaces and
two types of approaches, so uncertainty
remains in understanding the
relationship between estimated modeled
PM2.5 concentrations and design values
more broadly across hybrid modeling
studies. Moreover, this analysis was
completed using two hybrid modeling
methods that estimate PM2.5
concentrations in the U.S., thus an
additional uncertainty includes
understanding the relationship between
concentration, averaged over 3 years. For the 24hour standard, design values are calculated as the
98th percentile of the annual distribution of 24hour PM2.5 concentrations, averaged over three
years (appendix N of 40 CFR part 50).
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modeled PM2.5 concentrations and
design values reported in Canada.
In addition, where PM2.5 and other
pollutants (e.g., ozone, nitrogen dioxide,
and carbon monoxide) are correlated, it
can be difficult to distinguish whether
attenuation of effects in some studies
results from copollutant confounding or
collinearity with other pollutants in the
ambient mixture (U.S. EPA, 2019a,
section 1.5.1; U.S. EPA, 2022a, section
2.2.1). Studies evaluated in the 2019
ISA and ISA Supplement further
examined the potential confounding
effects of both gaseous and particulate
copollutants on the relationship
between long- and short-term PM2.5
exposure and health effects. As noted in
the Appendix (Table A–1) to the 2019
ISA (U.S. EPA, 2019a), copollutant
models are not without their limitations,
such as instances for which correlations
are high between pollutants resulting in
greater bias in results. However, the
studies continue to provide evidence
indicating that associations with PM2.5
are relatively unchanged in copollutants
models (U.S. EPA, 2019a, section 1.5.1;
U.S. EPA, 2022a, section 2.2.1).
Another area of uncertainty is
associated with other potential
confounders, beyond copollutants.
Some studies have expanded the
examination of potential confounders to
not only include copollutants, but also
systematic evaluations of the potential
impact of inadequate control from longterm temporal trends and weather (U.S.
EPA, 2019a, section 11.1.5.1). Analyses
examining these covariates further
confirm that the relationship between
PM2.5 exposure and mortality is unlikely
to be biased by these factors. Other
studies have explored the use of
alternative methods for confounder
control to more extensively account for
confounders and are more robust to
model misspecification that can further
inform the causality determination for
long-term and short-term PM2.5 and
mortality and cardiovascular effects
(U.S. EPA, 2019a, section 11.2.2.4; U.S.
EPA, 2022a, sections 3.1.1.3, 3.1.2.3,
3.2.1.2, and 3.2.2.3). These studies
indicate that bias from unmeasured
confounders can occur in either
direction, although controlling for these
confounders did not result in the
elimination of the association, but
instead provided additional support for
associations between long-term PM2.5
exposure and mortality when
accounting for additional confounders
(U.S. EPA, 2022a, section 3.2.2.2.6).
Another important limitation
associated with the evidence is that,
while epidemiologic studies indicate
associations between PM2.5 and health
effects, they do not identify particular
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PM2.5 exposures that cause effects.
Rather, health effects can occur over the
entire distribution of ambient PM2.5
concentrations evaluated, and
epidemiologic studies conducted to date
do not identify a population-level
threshold below which it can be
concluded with confidence that PM2.5related effects do not occur.
Overall, evidence assessed in the 2019
ISA and ISA Supplement continues to
indicate a linear, no-threshold C–R
relationship for PM2.5 concentrations >8
mg/m3. However, uncertainties remain
about the shape of the C–R curve at
PM2.5 concentrations <8 mg/m3, with
some recent studies providing evidence
for either a sublinear, linear, or
supralinear relationship at these lower
concentrations (U.S. EPA, 2019a,
section 11.2.4; U.S. EPA, 2022a, section
2.2.3.2).
There are also a number of
uncertainties and limitations associated
with the experimental evidence (i.e.,
controlled human exposure studies and
animal toxicological studies). With
respect to controlled human exposure
studies, the PA recognizes that these
studies include a small number of
individuals compared to epidemiologic
studies. Additionally, these studies tend
to include generally healthy adult
individuals, who are at a lower risk of
experiencing health effects. These
studies, therefore, often do not include
populations that are at increased risk of
PM2.5-related health effects, including
children, older adults, or individuals
with pre-existing conditions. As such,
these studies are somewhat limited in
their ability to inform at what
concentrations effects may be elicited in
at-risk populations. With respect to
animal toxicological studies, while
these studies often examine more severe
health outcomes and longer exposure
durations than controlled human
exposure studies, there is uncertainty in
extrapolating the effects seen in
animals, and the PM2.5 exposures and
doses that cause those effects, to human
populations.
C. Summary of Exposure and Risk
Estimates
Beyond the consideration of the
scientific evidence, discussed above in
section II.B, the EPA also considers the
extent to which new or updated
quantitative analyses of PM2.5 air
quality, exposure, or health risks could
inform conclusions on the adequacy of
the public health protection provided by
the current primary PM2.5 standards.
Conducting such quantitative analyses,
if appropriate, could inform judgments
about the potential for additional public
health improvements associated with
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PM2.5 exposure and related health
effects and could help to place the
evidence for specific effects into a
broader public health context.
In addition to consideration of the
scientific evidence, the PA includes an
at-risk analysis that assesses PM2.5attributable risk associated with PM2.5
air quality that has been adjusted to
simulate air quality scenarios of policy
interest (e.g., ‘‘just meeting’’ the current
or potential alternative standards).
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1. Key Design Aspects
Risk assessments combine data from
multiple sources and involve various
assumptions and uncertainties. Input
data for these analyses includes C–R
functions from epidemiologic studies
for each health outcome and ambient
annual or 24-hour PM2.5 concentrations
for the study areas utilized in the risk
assessment (U.S. EPA, 2022b, section
3.4.1). Additionally, quantitative and
qualitative methods were used to
characterize variability and uncertainty
in the risk estimates (U.S. EPA, 2022b,
section 3.4.1.7).
Concentration-response functions
used in the risk assessment are from
large, multicity U.S. epidemiologic
studies that evaluate the relationship
between PM2.5 exposures and mortality.
Epidemiologic studies and
concentration-response studies that
were used in the risk assessment to
estimate risk were identified using
criteria that take into account factors
such as study design, geographic
coverage, demographic populations, and
health endpoints (U.S. EPA, 2022b,
section 3.4.1.1).86 The risk assessment
focuses on all-cause or nonaccidental
mortality associated with long-term and
short-term PM2.5 exposures, for which
the 2019 ISA concluded that the
evidence provides support for a ‘‘causal
relationship’’ (U.S. EPA, 2022b, section
3.4.1.2).87
As described in more detail in the PA,
the risk assessment first estimated
health risks associated with air quality
for 2015 adjusted to simulate ‘‘just
meeting’’ the current primary PM2.5
standards (i.e., the annual standard with
its level of 12.0 mg/m3 and the 24-hour
standard with its level of 35 mg/m3). Air
quality modeling was then used to
simulate air quality just meeting an
86 Additional detail regarding the selection of
epidemiologic studies and specification of C–R
functions is provided in the PA (U.S. EPA, 2022b,
Appendix C, section C.1.1).
87 While the 2019 ISA also found that evidence
supports the determination of a ‘‘causal
relationship’’ between long- and short-term PM2.5
exposures and cardiovascular effects,
cardiovascular mortality was not included as a
health outcome as it will be captured in the
estimates of all-cause mortality.
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alternative standard with a level of 10.0
mg/m3 (annual) and 30 mg/m3 (24-hour).
In addition to the model-based
approach, for the subset of 30 areas
controlled by the annual standard linear
interpolation and extrapolation were
employed to simulate just meeting
alternative annual standards with levels
of 11.0 (interpolated between 12.0 and
10.0 mg/m3), 9.0 mg/m3, and 8.0 mg/m3
(both extrapolated from 12.0 and 10.0
mg/m3) (U.S. EPA, 2022b, section
3.4.1.3). The PA notes that there is
greater uncertainty regarding whether a
revised 24-hour standard (i.e., with a
lower level) is needed to further limit
‘‘peak’’ PM2.5 concentration exposure
and whether a lower 24-hour standard
level would most effectively reduce
PM2.5-associated health risks associated
with ‘‘typical’’ daily exposures. The risk
assessment estimates health risks
associated with air quality adjusted to
meet a revised 24-hour standard with a
level of 30 mg/m3, in conjunction with
estimating the health risks associated
with meeting a revised annual standard
with a level of 10.0 mg/m3 (U.S. EPA,
2022b, section 3.4.1.3). More details on
the air quality adjustment approaches
used in the risk assessment are
described in section 3.4.1.4 and
Appendix C of the PA (U.S. EPA,
2022b).
When selecting U.S. study areas for
inclusion in the risk assessment, the
available ambient monitors, geographic
diversity, and ambient PM2.5 air quality
concentrations were taken into
consideration (U.S. EPA, 2022b, section
3.4.1.4). When these factors were
applied, 47 urban study areas were
identified, which include nearly 60
million people aged 30–99, or
approximately 30% of the U.S
population in this age range (U.S. EPA,
2022b, section 3.4.1.5, Appendix C,
section C.1.3). Of the 47 study areas,
there were 30 study areas where just
meeting the current standards is
controlled by the annual standard,88 11
study areas where just meeting the
current standards is controlled by the
daily standard,89 and 6 study areas
where the controlling standard differed
depending on the air quality adjustment
88 For these areas, the annual standard is the
‘‘controlling standard’’ because when air quality is
adjusted to simulate just meeting the current or
potential alternative annual standards, that air
quality also would meet the 24-hour standard being
evaluated.
89 For these areas, the 24-hour standard is the
controlling standard because when air quality is
adjusted to simulate just meeting the current or
potential alternative 24-hour standards, that air
quality also would meet the annual standard being
evaluated. Some areas classified as being controlled
by the 24-hour standard also violate the annual
standard.
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approach (U.S. EPA, 2022b, section
3.4.1.5).90
In addition to the overall risk
assessment, the PA also includes an atrisk analysis and estimates exposures
and health risks of specific populations
identified as at-risk that would be
allowed under the current and potential
alternative standards to further inform
the Administrator’s conclusions
regarding the adequacy of the public
health protection provided by the
current primary PM2.5 standards. In so
doing, the PA evaluates exposure and
PM2.5 mortality risk for older adults
(e.g., 65 years and older), stratified for
White, Black, Asian, Native American,
Non-Hispanic, and Hispanic individuals
residing in the same study areas
included in the overall risk assessment.
This analysis utilizes a recent
epidemiologic study that provides raceand ethnicity-specific risk coefficients
(Di et al., 2017b).
2. Key Limitations and Uncertainties
Uncertainty in risk estimates (e.g., in
the size of risk estimates) can result
from a number of factors, including the
assumptions about the shape of the
C–R function with mortality at low
ambient PM concentrations, the
potential for confounding and/or
exposure measurement error in the
underlying epidemiologic studies, and
the methods used to adjust PM2.5 air
quality. More specifically, the use of air
quality modeling to adjust PM2.5
concentrations are limited as they rely
on model predictions, are based on
emission changes are scaled by fixed
percentages, and use only two of the full
set of possible emission scenarios and
linear interpolation/extrapolation to
adjust air quality that may not fully
capture potential non-linearities
associated with real-world changes in
air quality. Additionally, the selection
of case study areas is limited to urban
areas predominantly located CA and in
the Eastern U.S. that are controlled by
the annual standard. While the risk
assessment does not report quantitative
uncertainty in the risk estimates as
exposure concentrations are reduced, it
does provide information on the
distribution of concentrations associated
with the risk estimates when evaluating
progressively lower alternative annual
standards. Based on these data, as lower
alternative annual standards are
evaluated, larger proportions of the
distributions in risk occur at or below
10 mg/m3 (a concentrations which is
below or near most of the study reported
90 In these 6 areas, the controlling standard
depended on the air quality adjustment method
used and/or the standard scenarios evaluated.
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means from the key U.S. epidemiologic
studies) and at or below 8 mg/m3 (the
concentration at which the ISA reports
increasing uncertainty in the shape of
the C–R curve based on the body of
epidemiologic evidence). Similarly, the
at-risk analysis is also subject to many
of these same uncertainties.
Additionally, the at-risk analysis
included C–R functions from only one
study (Di et al., 2017b), which reported
associations between long-term PM2.5
exposures and mortality, stratified by
race/ethnicity, in populations age 65
and older, as opposed to the multiple
studies used in the overall risk
assessment to convey risk estimate
variability. These and other sources of
uncertainty in the overall risk
assessment and the at-risk analyses are
characterized in the PA (U.S. EPA, 2022,
section 3.4.1.7, section 3.4.1.8,
Appendix C, section C.3).
3. Summary of Risk Estimates
Although limitations in the
underlying data and approaches lead to
some uncertainty regarding estimates of
PM2.5-associated risk, the risk
assessment estimates that the current
primary PM2.5 standards could allow a
substantial number of PM2.5-associated
deaths in the U.S. For example, when
air quality in the 47 study areas is
adjusted to simulate just meeting the
current standards, the risk assessment
estimates up to 45,100 deaths in 2015
are attributable to long-term PM2.5
exposures associated with just meeting
the current annual and 24-hour PM2.5
standards (U.S. EPA, 2022, section
3.4.2.1). Additionally, as described in
more detail in the PA, the at-risk
analysis indicates that Black
populations may experience
disproportionally higher exposures and
risk under air quality conditions just
meeting the current primary annual
PM2.5 standard in the study areas, as
compared to White populations. Risk
disparities include exposure disparities,
as well as the relationship between
exposure and health effect and baseline
rates of the health effect. While risk
disparities may be a more meaningful
metric, they are also subject to
additional uncertainties.
Compared to the current annual
standard, meeting a revised annual
standard with a lower level is estimated
to reduce PM2.5-associated health risks
in the 30 study areas controlled by the
annual standard by about 7–9% a level
of 11.0 mg/m3, 15–19% for a level of
10.0 mg/m3, 22–28% for a level of 9.0
mg/m3, and 30–37% for a level of 8.0 mg/
m3) (U.S. EPA, 2022b, Table 3–17).
Meeting a revised annual standard with
a lower level may also reduce exposure
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and risk in Black populations slightly
more so than in White populations in
simulated scenarios just meeting
alternative annual standards. However,
though reduced, disparities by race and
ethnicity persist even at an alternative
annual standard level of 8 mg/m3, the
lowest alternative annual standard
included in the risk assessment (U.S.
EPA, 2022b, section 3.4.2.4).
Revising the level of the 24-hour
standard to 30 mg/m3 is estimated to
lower PM2.5-associated risks across a
more limited population and number of
areas then revising the annual standard
(U.S. EPA, 2022, section 3.4.2.4). Risk
reduction predictions are largely
confined to areas located in the western
U.S., several of which are also likely to
experience risk reductions upon
meeting a revised annual standard. In
the 11 areas controlled by the 24-hour
standard, when air quality is simulated
to just meet the current 24-hour
standard, PM2.5 exposures are estimated
to be associated with as many as 2,570
deaths annual. Compared to just
meeting the current standard, air quality
just meeting an alternative 24-hour
standard level of 30 mg/m3 is associated
with reductions in estimated risk of 9–
13% (U.S. EPA, 2022b, section 3.4.2.3).
D. Proposed Conclusions on the Primary
PM2.5 Standards
In reaching proposed conclusions on
the current primary PM2.5 standards
(presented in section II.D.3), the
Administrator has taken into account
the current evidence and associated
conclusions in the 2019 ISA and ISA
Supplement, in light of the policyrelevant evidence-based and risk-based
considerations discussed in the PA
(summarized in section II.D.2), as well
as advice from the CASAC, and public
comment received on the standards thus
far in the reconsideration (section
II.D.1). In general, the role of the PA is
to help ‘‘bridge the gap’’ between the
Agency’s assessment of the current
evidence and quantitative analyses (of
air quality, exposure, and risk), and the
judgments required of the Administrator
in determining whether it is appropriate
to retain or revise the NAAQS.
Evidence-based considerations draw
upon the EPA’s integrated assessment of
the scientific evidence of health effects
related to PM2.5 exposure presented in
the 2019 ISA and ISA Supplement
(summarized in section II.B above) to
address key policy-relevant questions in
the reconsideration. Similarly, the riskbased considerations draw upon the
assessment of population exposure and
risk (summarized in section II.C above)
in addressing policy-relevant questions
focused on the potential for PM2.5
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exposures associated with mortality
under air quality conditions just
meeting the current and potential
alternative standards.
The approach to reviewing the
primary standards is consistent with
requirements of the provisions of the
CAA related to the review of the
NAAQS and with how the EPA and the
courts have historically interpreted the
CAA. As discussed in section I.A above,
these provisions require the
Administrator to establish primary
standards that, in the Administrator’s
judgment, are requisite (i.e., neither
more nor less stringent than necessary)
to protect public health with an
adequate margin of safety. Consistent
with the Agency’s approach across all
NAAQS reviews, the EPA’s approach to
informing these judgments is based on
a recognition that the available health
effects evidence generally reflects a
continuum that includes ambient air
exposures for which scientists generally
agree that health effects are likely to
occur through lower levels at which the
likelihood and magnitude of response
become increasingly uncertain. The
CAA does not require the Administrator
to establish a primary standard at a zerorisk level or at background
concentration levels, but rather at level
that reduces risk sufficiently so as to
protect public health, including the
health of sensitive groups, with an
adequate margin of safety.
The proposed decisions on the
adequacy of the current primary PM2.5
standards described below is a public
health policy judgment by the
Administrator that draws on the
scientific evidence for health effects,
quantitative analyses of population
exposures and/or health risks, and
judgments about how to consider the
uncertainties and limitations that are
inherent in the scientific evidence and
quantitative analyses. The four basic
elements of the NAAQS (i.e., indicator,
averaging time, form, and level) have
been considered collectively in
evaluating the public health protection
afforded by the current standards. The
Administrator’s final decisions will
additionally consider public comments
received on these proposed decisions.
1. CASAC Advice in This
Reconsideration
The CASAC has provided advice on
the adequacy of the current primary
PM2.5 standards in the context of its
review of the draft PA.91 The range of
91 A limited number of public comments have
also been received in this reconsideration to date,
including comments focused on the draft PA. Of the
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views summarized here generally
reflects differing judgments as to the
relative weight to place on various types
of evidence, the risk-based information,
and the associated uncertainties, as well
as differing judgments about the
importance of various PM2.5-related
health effects from a public health
perspective.
In its comments on the draft PA, the
CASAC stated that: ‘‘[o]verall the
CASAC finds the Draft PA to be wellwritten and appropriate for helping to
‘bridge the gap’ between the agency’s
scientific assessments and quantitative
technical analyses, and the judgments
required of the Administrator in
determining whether it is appropriate to
retain or revise the National Ambient
Air Quality Standards (NAAQS)’’
(Sheppard, 2022a, p. 1 of consensus
letter). The CASAC also stated that the
‘‘[d]raft PA adequately captures and
appropriately characterizes the key
aspects of the evidence assessed and
integrated in the 2019 ISA and Draft ISA
Supplement of PM2.5-related health
effects’’ (Sheppard, 2022b, p. 2 of
consensus letter). The CASAC also
stated that ‘‘[t]he interpretation of the
risk assessment for the purpose of
evaluating the adequacy of the current
primary PM2.5 annual standard is
appropriate given the scientific findings
presented’’ (Sheppard, 2022a, p. 2 of
consensus letter). The CASAC also
stated that the ‘‘[d]raft PA adequately
captures and appropriately characterizes
the key aspects of the evidence assessed
and integrated in the 2019 ISA and Draft
ISA Supplement of PM2.5-related health
effects’’ (Sheppard, 2022a, p. 2 of
consensus letter). The CASAC also
stated that ‘‘[t]he interpretation of the
risk assessment for the purpose of
evaluating the adequacy of the current
primary PM2.5 annual standard is
appropriate given the scientific findings
presented’’ (Sheppard, 2022a, p. 2 of
consensus letter).
With regard to the adequacy of the
current primary annual PM2.5 standard,
‘‘all CASAC members agree that the
current level of the annual standard is
not sufficiently protective of public
health and should be lowered’’
(Sheppard, 2022a, p. 2 of consensus
letter). Additionally, ‘‘the CASAC
reached consensus that the indicator,
form, and averaging time should be
retained, without revision’’ (Sheppard,
2022a, p. 2 of consensus letter). With
regard to the level of the primary annual
PM2.5 standard, the CASAC had
public comments that addressed adequacy of the
current primary PM2.5 standards, some expressed
agreement with staff conclusions in the draft PA,
while others expressed the view that the standards
should be more stringent.
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differing recommendations for the
appropriate range for an alternative
level. The majority of the CASAC
‘‘judge[d] that an annual average in the
range of 8–10 mg/m3’’ was most
appropriate, while the minority of the
CASAC members stated that ‘‘the range
of the alternative standard of 10–11 mg/
m3 is more appropriate’’ (Sheppard,
2022a, p. 16 of consensus responses).
The CASAC did highlight, however, that
‘‘the alternative standard level of 10 mg/
m3 is within the range of acceptable
alternative standards recommended by
all CASAC members, and that an annual
standard below 12 mg/m3 is supported
by a larger and coherent body of
evidence’’ (Sheppard, 2022a, p. 16 of
consensus responses).
In reaching conclusions on a
recommended range of 8–10 mg/m3 for
the primary annual PM2.5 standard, the
majority of the CASAC placed weight on
various aspects of the available
scientific evidence and quantitative risk
assessment information (Sheppard,
2022a, p. 16 of consensus responses). In
particular, these members cited recent
U.S.- and Canadian-based epidemiologic
studies that show positive associations
between PM2.5 exposure and mortality
with study-reported means below 10 mg/
m3. Further, these members also noted
that the lower portions of the air quality
distribution (i.e., concentrations below
the mean) provide additional
information to support associations
between health effects and PM2.5
concentrations lower than the long-term
mean concentration. In addition, the
CASAC members recognized that the
available evidence has not identified a
threshold concentration, below which
an association no longer remains,
pointing to the conclusion in the draft
ISA Supplement that the ‘‘evidence
remains clear and consistent in
supporting a no-threshold relationship,
and in supporting a linear relationship
for PM2.5 concentrations >8 mg/m3’’
(Sheppard, 2022a, p. 16 of consensus
responses). Finally, these CASAC
members placed weight on the at-risk
analysis as providing support for
protection of at-risk demographic
groups, including minority populations.
In reaching conclusions on a
recommended range of 10–11 mg/m3 for
the primary annual PM2.5 standard, the
minority of the CASAC emphasized that
there were few key epidemiologic
studies that reported positive and
statistically significant health effects
associations for PM2.5 air quality
distributions with overall mean
concentrations below 9.6 mg/m3
(Sheppard, 2022a, p. 17 of consensus
responses). In so doing, the minority of
the CASAC specifically noted the
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variability in the relationship between
study-reported means and area annual
design values based on the methods
utilized in the studies, noting that
design values are generally higher than
area average exposure levels. Further,
the minority of the CASAC stated that
‘‘uncertainties related to copollutants
and confounders make it difficult to
justify a recommendation below 10–11
mg/m3’’ (Sheppard, 2022a, p. 17 of
consensus responses). Finally, the
minority of the CASAC placed less
weight on the risk assessment results,
noting large uncertainties, including the
approaches used for adjusting air
quality to simulate just meeting the
current and alternative standards.
With regard to the current primary 24hour PM2.5 standard, the CASAC did not
reach consensus regarding the adequacy
of the public health protection provided
by the current standard. The majority of
the CASAC members concluded ‘‘that
the available evidence calls into
question the adequacy of the current 24hour standard’’ (Sheppard, 2022a, p. 3
of consensus letter), while the minority
of the CASAC members agreed with
‘‘the EPA’s preliminary conclusion [in
the draft PA] to retain the current 24hour PM2.5 standard without revision’’
(Sheppard, 2022a, p. 4 of consensus
letter). The CASAC recommended that
in future reviews, the EPA also consider
alternative forms for the primary 24hour PM2.5 standard. Specifically, the
CASAC ‘‘suggests considering a rolling
24-hour average and examining
alternatives to the 98th percentile of the
3-year average,’’ pointing to concerns
that computing 24-hour average PM2.5
concentrations using the current
midnight-to-midnight timeframe could
potentially underestimate the effects of
high 24-hour exposures, especially in
areas with wood-burning stoves and
wintertime stagnation (Sheppard, 2022a,
p. 18 of consensus responses).
The majority of the CASAC favored
revising the level of the primary 24-hour
PM2.5 standard and suggested that a
range of 25–30 mg/m3 would be
adequately protective. In so doing, the
CASAC placed weight on the available
epidemiologic evidence, including
epidemiologic studies that restricted
analyses to 24-hour PM2.5
concentrations below 25 mg/m3. These
members also placed weight on results
of controlled human exposure studies
with exposures close to the current
standard, which they note provide
support for the epidemiologic evidence
to lower the standard. These members
noted the limitations in using controlled
human exposure studies alone in
considering adequacy of the 24-hour
standard, recognizing that controlled
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human exposure studies preferentially
recruit less susceptible individuals and
have a typical exposure duration much
shorter than 24 hours. These members
also placed ‘‘greater weight on the
scientific evidence than on the values
estimated by the risk assessment,’’ citing
their concerns that the risk assessment
‘‘may not adequately capture areas with
wintertime stagnation and residential
wood-burning where the annual
standard is less likely to be protective’’
(Sheppard, 2022a, p. 17 of consensus
responses). Furthermore, these CASAC
members ‘‘also are less confident that
the annual standard could adequately
protect against health effects of shortterm exposures’’ (Sheppard, 2022a, p.
17 of consensus responses).
The minority of the CASAC agreed
with the EPA’s preliminary conclusion
in the draft PA to retain the current
primary 24-hour PM2.5 standard,
without revision. In so doing, the
minority of the CASAC placed greater
weight on the risk assessment, noting
that the risk assessment accounts for
both the level and the form of the
current standard and the way
attainment with the standard is
determined. Further, the minority of the
CASAC stated that the ‘‘risk assessment
indicates that the annual standard is the
controlling standard across most of the
urban study areas evaluated and
revising the level of the 24-hour
standard is estimated to have minimal
impact on the PM2.5-associated risks’’
and that, because of this, ‘‘the annual
standard can be used to limit both longand short-term PM2.5 concentrations’’
(Sheppard, 2022a, p. 18 of consensus
responses). Further, the minority of the
CASAC placed more weight on the
controlled human exposure studies,
which show ‘‘effects at PM2.5
concentrations well above those
typically measured in areas meeting the
current standards’’ and which suggest
that ‘‘the current standards are
providing adequate protection against
these exposures’’ (Sheppard, 2022a, p.
18 of consensus responses).
While the CASAC members expressed
differing opinions on the appropriate
revisions to the current standards, they
did ‘‘find that both primary standards,
24-hour and annual, are critical to
protect public health given the evidence
on detrimental health outcomes at both
short-term and long-term exposures
including peak events’’ (Sheppard,
2022a, p. 13 of consensus responses).
The comments from the CASAC also
took note of uncertainties that remain in
this reconsideration of the primary
PM2.5 standards and they identified a
number of additional areas for future
research and data gathering that would
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inform future reviews of the primary
PM2.5 NAAQS (Sheppard, 2022a, pp.
14–15 of consensus responses).
2. Evidence- and Risk-Based
Considerations in the Policy Assessment
The main focus of the policy-relevant
considerations in the PA is
consideration of the question: Does the
currently available scientific evidenceand exposure/risk-based information
support or call into question the
adequacy of the protection afforded by
the current primary PM2.5 standards?
The PA response to this overarching
question takes into account discussions
that address the specific policy-relevant
questions for this reconsideration,
focusing first on consideration of the
scientific evidence, as evaluated in the
2019 ISA and ISA Supplement,
including that newly available in this
reconsideration (section II.D.2.a). The
PA also considers the quantitative risk
estimates drawn from the risk
assessment (presented in detail in
section 3.4 and Appendix C of the PA;
U.S. EPA, 2022b) including associated
limitations and uncertainties, and the
extent to which they may indicate
different conclusions from those in
previous reviews regarding the
magnitude of risk, as well as the level
of protection from adverse effects,
associated with the current and
alternative standards (section II.D.2.b).
The PA additionally considers the key
aspects of the evidence and exposure/
risk estimates that were emphasized in
previous reviews of the current
standards, as well as the associated
public health policy judgments and
judgments about the uncertainties
inherent in the scientific evidence and
quantitative analyses that are integral to
consideration of whether the currently
available information supports or calls
into question the adequacy of the
current primary PM2.5 standards (U.S.
EPA, 2022b, section 3.6).
a. Evidence-Based Considerations
The currently available evidence on
the health effects of PM2.5, including
evidence newly available in this
reconsideration, is largely consistent
with the evidence that was available in
previous reviews regarding health
effects causally related to PM2.5
exposures. Specifically, as in the 2012
review, mortality and cardiovascular
effects are concluded to be causally
related to long- and short-term
exposures to PM2.5, while respiratory
effects are concluded to likely be
causally related to long- and short-term
PM2.5 exposures. Also, since the 2012
review, recent evidence provides
additional support that is sufficient to
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5609
conclude that the relationship between
long-term PM2.5 exposures and nervous
system effects and cancer are likely to
be causal (U.S. EPA, 2019a, Table ES–
1). These determinations are based on
evidence from experimental and
epidemiologic studies that is newly
available since the completion of the
2009 ISA (U.S. EPA, 2019, Table ES–1).
The current evidence base is concluded
to be suggestive of, but not sufficient to
infer, causal relationships between
nervous system effects and short-term
PM2.5 exposures; metabolic effects,
reproduction and fertility, and
pregnancy and birth outcomes and longand short-term PM2.5 exposures (U.S.
EPA, 2019a, Table ES–1). Additionally,
the current evidence base supports a
suggestive of, but not sufficient to infer,
a causal relationship for cardiovascular
effects and short-term UFP exposures;
respiratory effects and short-term UFP
exposures; and nervous system effects
and long- and short-term exposures
(U.S. EPA, 2019a, Table ES–1).
The available evidence in the 2019
ISA continues to provide support for
factors that may contribute to increased
risk of PM2.5-related health effects
including lifestage (children and older
adults), pre-existing diseases
(cardiovascular disease and respiratory
disease), race/ethnicity, and SES. Other
factors that have the potential to
contribute to increased risk, but for
which the evidence is less clear, include
obesity, diabetes, genetic factors,
smoking status, sex, diet, and residential
location (U.S. EPA, 2019a, chapter 12).
In addition to these population groups,
the 2019 ISA and ISA Supplement
conclude that there is strong evidence
for racial and ethnic differences in PM2.5
exposures and PM2.5-related health risk.
There is strong evidence demonstrating
that Black and Hispanic populations, in
particular, have higher PM2.5 exposures
than non-Hispanic White populations
(U.S. EPA, 2019a, Figure 12–2; U.S.
EPA, 2022a, Figure 3–38). Further, there
is consistent evidence across multiple
studies that demonstrate increased risk
of PM2.5-related health effects for Black
populations, with the strongest evidence
for health risk disparities for mortality
(U.S. EPA, 2019a, section 12.5.4). In
addition, studies assessed in the 2019
ISA and ISA Supplement also provide
evidence of exposure and health risk
disparities based on SES. The evidence
indicates that lower SES communities
are exposed to higher concentrations of
PM2.5 compared to higher SES
communities (U.S. EPA, 2019a, section
12.5.3; U.S. EPA, 2022b, section
3.3.3.1.1). Additionally, evidence
supports the conclusions that lower SES
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is associated with cause-specific
mortality and certain health endpoints
(i.e., MI and CHF), but less so for allcause or total (non-accidental) mortality
(U.S. EPA, 2019a, section 12.5.3; U.S.
EPA, 2022b, section 3.3.3.1).
Consistent with the evidence
available in the 2009 ISA, controlled
human exposure studies have
demonstrated effects on cardiovascular
function following 1- to 5-hour
exposures to PM2.5, with the most
consistent evidence for impaired
vascular function. The PA notes that
most of the controlled human exposure
studies have evaluated average PM2.5
concentrations at or above about 100 mg/
m3, with exposure durations up to two
hours. These studies have often, though
not always, reported statistically
significant effects on one or more
indicators of cardiovascular function
following 2-hour exposures to average
PM2.5 concentrations at and above about
120 mg/m3, with less consistent effects
following exposures to concentrations
lower than 120 mg/m3.
In considering the controlled human
exposure studies in reaching
conclusions on the primary PM2.5
standards, the PA notes that air quality
analyses indicate that 2-hour PM2.5
concentrations to which individuals
were exposed in most of these studies,
including those that report the most
consistent results, are well-above the
ambient PM2.5 concentrations typically
measured in locations meeting the
current primary standards.
Additionally, the PA recognizes that the
results are variable across controlled
human exposure studies that evaluated
near-ambient PM2.5 concentrations.
Furthermore, the PA recognizes that
controlled human exposure studies
often include small numbers of
individuals and do not include
populations that are at increased risk of
PM2.5-related health effects (e.g.,
children). While the PA recognizes that
the controlled human exposure studies
are important in establishing biological
plausibility, it emphasizes that it is
unclear how the results from these
studies alone, particularly in studies
conducted at near-ambient PM2.5
concentrations, and the importance of
the effects observed in the studies
should be interpreted with respect to
adversity to public health.
With regard to the animal
toxicological studies, the PA recognizes
that, unlike the controlled human
exposure studies that provide insight on
the exposure concentrations that
directly elicit health effects in humans,
there is uncertainty associated with
translating the observations in the
animal toxicological studies to potential
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adverse health effects in humans. The
PA notes that the interpretation of these
studies is complicated by the fact that
PM2.5 concentrations in animal
toxicological studies are much higher
than those shown to elicit effects in
human populations. Moreover, the PA
recognizes that there are also significant
anatomical and physiological difference
between animal models and humans. In
considering the information from the
animal toxicological studies, the PA
specifically notes two studies, one of
which is newly available in the 2019
ISA, that report serious effects following
long-term exposures to PM2.5
concentrations close to the ambient
concentrations reported in some
epidemiologic studies, although still
above the ambient concentrations likely
to occur in areas meeting the current
primary standards (U.S. EPA, 2022b,
section 3.3.3.1).
Since the 2012 review, a large number
of epidemiologic studies have become
available that report generally positive,
and often statistically significant,
associations between long- and shortterm PM2.5 exposures and mortality and
morbidity. Available studies
additionally indicate that PM2.5 health
effect associations are robust across
various approaches to estimating PM2.5
exposures and across various exposure
windows. Since the 2012 review, there
are also a number of studies that employ
alternative methods for confounder
control that further inform the causal
nature of the relationship between longor short-term term PM2.5 exposure and
mortality, and these studies provide
support for the findings from the broad
body of epidemiologic studies.
In addition to broadening our
understanding of the health effects that
can result from exposures to PM2.5 and
strengthening support for some key
effects (e.g., nervous system effects,
cancer, and metabolic effects), recent
epidemiologic studies strengthen
support for health effect associations at
relatively low ambient PM2.5
concentrations. Studies that examine
the shapes of C–R functions over the full
distribution of ambient PM2.5
concentrations have not identified a
threshold concentration below which
associations no longer exist (U.S. EPA,
2019a, section 1.5.3; U.S. EPA, 2022a,
sections 2.2.3.1 and 2.2.3.2). While such
analyses are complicated by the
relatively sparse data available at the
lower end of the air quality distribution
(U.S. EPA, 2019a, section 1.5.3), the
evidence remains consistent in
supporting a no-threshold relationship,
and in supporting a linear relationship
for PM2.5 concentrations >8 mg/m3.
However, uncertainties remain about
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the shape of the C–R curve at PM2.5
concentrations <8 mg/m3, with some
recent studies providing evidence for
either a sublinear, linear, or supralinear
relationship at these lower
concentrations.
Consistent with previous reviews, the
PA notes that the use of information
from epidemiologic studies to inform
conclusions on the current standards is
complicated by the fact that such
studies evaluate associations between
distributions of ambient PM2.5 and
health outcomes, and do not identify the
specific exposures that can lead to the
reported effects. Rather, health effects
can occur over the entire distribution of
ambient PM2.5 concentrations evaluated,
and epidemiologic studies do not
identify a population-level threshold
below which it can be concluded with
confidence that PM-associated health
effects do not occur (U.S. EPA, 2019a,
section 1.5.3). However, the studyreported ambient PM2.5 concentrations
reflecting estimated exposure in the
middle portion of the PM2.5 air quality
distribution, which corresponds to the
bulk of the underlying data, provide the
strongest support for reported health
effect associations and can inform
conclusions on the current and potential
alternative standards. In considering
this information, the PA recognizes that
the mean PM2.5 concentrations reported
by key epidemiologic studies differ in
how mean concentrations were
calculated, as well as their
interpretation in what means represent
in the context of the current standards.
In identifying key epidemiologic
studies for consideration, the PA places
the greatest emphasis on studies
conducted in the U.S. and Canada,
although recognizes a number of
limitations associated with interpreting
the results of Canadian studies
compared to studies conducted in the
U.S. Generally, there are differences in
the exposure environments and
population characteristics between the
U.S. and other countries, including
Canada, that can affect the studyreported mean PM2.5 concentration and
its comparability with the annual
standard level. A number of other
differences, including sources and
pollutant mixtures, concentration
gradients, and populations densities,
can make it challenging to interpret the
mean PM2.5 concentrations in Canadian
studies in the context of a U.S.-based
standard. Specifically, it may be
difficult to use such studies to directly
and quantitatively inform questions
regarding the adequacy of the current or
potential alternative levels of the annual
standard. Therefore, while the PA
considers the mean PM2.5
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concentrations from U.S. and Canadian
studies in reaching conclusions, it notes
that the U.S.-based epidemiologic
studies are most informative for
comparisons with the annual standard
metric and for reaching conclusions on
the current standards and for informing
potential alternative levels of the
standard.
Consistent with previous reviews, in
considering information that can be
used from the available epidemiologic
evidence to inform proposed decisions
on the current standards, the PA focuses
on PM2.5 concentrations near or
somewhat below long-term mean
concentrations reported in
epidemiologic studies. In so doing, the
PA notes that, in previous reviews, the
epidemiologic studies used groundbased monitors to estimate exposures,
and that, in addition to newly available
monitor-based studies, there are also
newly available epidemiologic studies
estimate exposures using hybrid
modeling approaches. In considering
how the study-reported mean PM2.5
concentrations reported in studies using
hybrid modeling approaches compare to
studies using ground-based monitors,
the PA notes that the hybrid modeling
approaches provide a broader
estimation of PM2.5 exposures compared
to monitor-based studies (i.e., because
hybrid modeling studies include PM2.5
concentrations estimated in areas
without monitors). However, compared
to monitor-based studies, the PA
recognizes that it is more difficult to
relate these means to an annual
standard metric which relies on
maximum monitor design values to
assess compliance. Further complicating
the comparison is the variability in how
PM2.5 concentrations are estimated
between studies that use hybrid
modeling approaches. Two important
variations across studies include: (1)
variability in spatial scale used (i.e.,
averages computed across the national
(or large portions of the country) versus
a focus on only CBSAs) and (2)
variability in exposure assignment
methods (i.e., averaging across all grid
cells, averaging across a scaled-up area
like a ZIP code, and population
weighting).
As described in more detail in section
I.D.5 above, the PA included analyses
that considered how the study-reported
mean PM2.5 concentrations were
computed and how the means compare
to the annual standard metric (including
the level, averaging time, and form) and
the use of the monitor with the highest
PM2.5 design value in an area for
compliance. In so doing, the PA
included a comparison of PM2.5 fields in
estimating exposure relative to design
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values using two hybrid modeling
surface with annual average PM2.5
concentrations estimated per year at a 1
km x 1 km spatial resolution. The PA
notes that the means vary when PM2.5
concentrations are estimated in urban
areas only (CBSAs) versus when the
averages were calculated with all or
most grid cells nationwide. This is
likely indicative of the fact that areas
included outside of CBSAs tend to be
more rural and have lower estimated
PM2.5 concentrations. The PA
acknowledges that this is an important
consideration since the study areas
included in the calculation of the mean,
and more specifically whether a study is
focused on nationwide, regional, or
urban areas, will affect the calculation
of the study mean based on how many
rural areas are included with lower
estimated PM2.5 concentrations. While
the determination of what spatial scale
to use to estimate PM2.5 concentrations
does not inherently affect the quality of
the epidemiologic study, the spatial
scale can influence the calculated longterm mean concentration across the
study area and period.
Additionally, the PA analyses
indicate that for the studies using the
hybrid modeling approaches, the use of
population weighting in calculating
study-reported mean PM2.5
concentrations, and not a difference in
estimates of exposures in the study
itself, can produce substantially
different study-reported mean PM2.5
concentrations compared to an
approach that does not utilize
population weighting. In studies that do
not apply population weighting in the
calculation of the mean PM2.5
concentrations, study-reported means
are lower, as a result of including areas
with lower estimated PM2.5
concentrations that may not be as
densely populated, as well as areas that
may not include health events. To
elaborate, in hybrid modeling
approaches that present mean PM2.5
concentrations based on an average
PM2.5 concentration across all grid cells
(i.e., do not apply aspects of population
weighting), health events may not exist
in each grid cell, and thus the mean
reported PM2.5 concentration is not
necessarily based on the mean PM2.5
concentrations assigned as the exposure
in the health study. In other words, the
mean PM2.5 concentration that is
reported and based on an average of all
grid cells is not necessarily the same as
the mean PM2.5 concentration for each
person assigned an exposure in the
study. This is an important
consideration, as the purpose of the
epidemiologic study is to evaluate
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whether an association between PM2.5
exposure and health outcomes exists. As
such, it is unclear whether the mean
concentration reported using each grid
cell is associated with a health outcome
(i.e., not all grid cells have health
events). This leads to uncertainty in
evaluating how the mean concentration
can be used in the context of the
approach above to evaluate the
adequacy of the standard as well as
potential alternative levels of the annual
standard.
In considering the variability in how
exposure in estimated between studies
that use hybrid modeling approaches,
the PA focuses on the key epidemiologic
studies that use hybrid modeling
approaches and apply population
weighting in calculating the studyreported mean, as well as those studies
that use monitors to estimate exposure,
as described in more detail in section
II.B.3.b above. For key U.S.
epidemiologic studies that use monitors
to estimate PM2.5 exposures, overall
mean PM2.5 concentrations range
between 9.9 mg/m3 92 to 16.5 mg/m3 (U.S.
EPA, 2022b, Figure 3–8). For U.S.
studies that use hybrid model-predicted
exposures and apply aspects of
population weighting, mean PM2.5
concentrations range from 9.3 mg/m3 to
12.2 mg/m3 (U.S. EPA, 2022b, Figure 3–
14). In U.S. studies that average up from
the grid cell level to the ZIP code or
census tract level, mean PM2.5
concentrations range from 9.8 mg/m3 to
12.2 mg/m3. In the one U.S. study that
population-weighted the grid cells prior
to averaging up to the ZIP code or
census tract level, the reported mean
PM2.5 concentration is 9.3 mg/m3. As
described above, the PA also considers
the study-reported means from the key
Canadian epidemiologic studies, which
are consistently much lower than those
reported for key U.S. epidemiologic
studies, while noting that for the
reasons described above, there are
uncertainties and limitations associated
with comparisons between Canadian
studies and the annual standard metric.
For the key Canadian epidemiologic
studies that use monitors to estimate
PM2.5 exposures, overall mean PM2.5
concentrations range from 6.9 mg/m3 to
13.3 mg/m3, while the range of mean
PM2.5 concentrations in Canadian
studies that use hybrid modeling (all of
which average up to postal codes and
thus include some aspects of population
weighting) is 5.9 mg/m3 to 9.8 mg/m3.
92 This is generally consistent with, but slightly
below, the lowest study-reported mean PM2.5
concentration from monitor-based studies available
in the 2020 PA, which was 10.7 mg/m3 (U.S. EPA,
2020a, Figure 3–7).
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As described in more detail in section
II.B.3.b above, in assessing the range of
reported exposure concentrations for
which the strongest support exists for
adverse health effects occurring, the PA
evaluates whether the available
evidence supports or calls into question
the adequacy of public health protection
afforded by the current primary annual
PM2.5 standard against these exposure
concentrations. This means, as in past
reviews, the application of a decision
framework based on assessing means
reported in key epidemiologic studies
must also consider how the study means
were computed and how these values
compare to the annual standard metric
(including the level, averaging time and
form) and the use of the monitor with
the highest PM2.5 design value in an area
for compliance. Based on the air quality
analyses in presented in the PA and
discussed above (section I.D.5.a and
section I.D.5.b), design values associated
with the study-reported means in these
key U.S. based epidemiologic studies
are only somewhat higher: 10–20% for
monitor-based studies and 15–18%
higher for the studies that include
hybrid modeling approaches and utilize
population weighting. Based on these
results, it can generally be concluded
that the study-reported mean
concentrations in the studies are
associated with air quality conditions
that would be achieved by meeting
annual standard levels that are 10–20%
higher and 15–18% higher than studyreported means for monitor-based
studies and hybrid modeling-based
studies that use population weighting,
respectively. Therefore, an annual
standard level that is no more than 10–
20% higher than the study-reported
means in the monitor-based studies (i.e.,
9.9–16.5 mg/m3), and no more than 15–
18% higher than the study-reported
means in the studies that include hybrid
modeling approaches and utilize
population weighting (i.e., 9.3–12.2 mg/
m3), would generally maintain air
quality exposures at or below those
associated with the study-reported mean
PM2.5 concentrations, exposures for
which we have the strongest support for
adverse health effects occurring. This
relationship is indicative of the fact that
PM2.5 exposures in an area are
represented by a distribution of
concentrations across that area, with the
annual standard level at the design
value monitor being associated with the
highest annual average exposure
concentration for that area.
In addition to the study-reported
mean concentrations, in considering the
level of the annual standard, the PA
uses an approach consistent with that
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used in previous reviews and also
considers reported PM2.5 concentrations
corresponding to the 25th and 10th
percentiles of health data or exposure
estimates when available in the key
epidemiologic studies. In using such an
approach, the PA recognized that there
is an interrelatedness of the
distributional statistics in epidemiologic
studies (e.g., 10th and 25th percentiles
of PM2.5 concentrations) and a range of
one standard deviation around the mean
which contains approximately 68% of
normally distributed data, in that one
standard deviation below the mean falls
between the 25th and 10th percentiles
(U.S. EPA, 2022b, p. 2–71). Further, the
PA notes that in past reviews, some
weight was placed on studies that
provided mean PM2.5 concentrations
around the 25th percentile of the
distributions of deaths and
cardiovascular-related hospitalizations
and the Administrator judged the region
around the 25th percentile as a
reasonable part of the distribution to
guide the decision on the appropriate
standard level (78 FR 3161, January 15,
2013).
As such, the PA concludes that
focusing on concentrations somewhat
below the means (e.g., 25th and 10th
percentiles), when such information is
available from epidemiologic studies, is
a reasonable approach for considering
lower portions of the air quality
distribution. However, the PA
recognizes that the health data are
appreciably more sparse and an
understanding of the magnitude and
significance of the associations
correspondingly become more uncertain
in the lower part of the air quality
distribution. While health effects can
occur over the entire distribution of
ambient PM2.5 concentrations evaluated,
and epidemiologic studies do not
identify a population-level threshold
below which it can be concluded with
confidence that PM-associated health
effects do not occur (U.S. EPA, 2019a,
section 1.5.3), using values below the
10th percentile would lead to even
greater uncertainties and diminished
confidence in the magnitude and
significance of the associations.
In considering the available key U.S.
epidemiologic studies, the PA notes that
a small number of studies report PM2.5
concentrations corresponding to the
25th and 10th percentiles of health data
or exposure estimates that can be
considered to provide insight into the
concentrations that comprise the lower
quartiles of the air quality distributions
is examined below. In studies that use
monitors to estimate PM2.5 exposures,
25th percentiles of health events
correspond to PM2.5 concentrations (i.e.,
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averaged over the study period for each
study city) at or above 11.5 mg/m3 and
10th percentiles of health events
correspond to PM2.5 concentrations at or
above 9.8 mg/m3 (i.e., 25% and 10% of
health events, respectively, occur in
study locations with PM2.5
concentrations below these values) (U.S.
EPA, 2022b, Figure 3–8). Of the key U.S.
epidemiologic studies that use hybrid
modeling approaches to estimate longterm PM2.5 exposures, the ambient PM2.5
concentrations corresponding to 25th
percentiles of estimated exposures are
9.1 mg/m3 (U.S. EPA, 2022b, Figure 3–
14). In key U.S. epidemiologic studies
that use hybrid modeling approaches to
estimate short-term PM2.5 exposures, the
ambient concentrations corresponding
to 25th percentiles of estimated
exposures, or health events, are 6.7 mg/
m3 and the ambient PM2.5 concentration
corresponding to that 10th percentile
range from 4.7 mg/m3 to 7.3 mg/m3 (U.S.
EPA, 2022b, Figure 3–14).
As with the mean PM2.5
concentrations, in considering these
values relative to an area annual design
value, the PA notes the 25th and 10th
percentiles provide information about
the lower quartiles of the air quality
distributions, while the study-reported
mean provides information about the
average or typical exposures, and the
corresponding area annual design value
provides the highest average annual
PM2.5 concentration being measured. In
this way, the PA recognizes that all of
these metrics (i.e., lower percentiles,
study mean, annual design value) have
a relationship relative to the other, and
each of these metrics can be used to
inform the consideration of the level of
the current annual standard. Further,
the PA recognizes that the air quality
analyses described above (section I.D.5)
and in the PA (U.S. EPA, 2022b, section
2.3.3.1 and section 2.3.3.2.4) that
evaluated the relationship between a
mean PM2.5 concentration in an area and
the design value focuses on mean PM2.5
concentrations and similar analyses
were not conducted for other PM2.5
concentrations in the lower portion of
the air quality distribution. Therefore,
given the lack of additional information
regarding the relationship between
percentiles of the air quality distribution
other than the mean and the annual
design value, the PA concludes that any
direct comparison of study-reported
PM2.5 concentrations corresponding to
lower percentiles (e.g., 25th and/or
10th) and annual design values is more
uncertain than such comparisons with
the mean.
Since the completion of the 2009 ISA,
a number of epidemiologic studies have
become available that can provide
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additional consideration to inform
conclusions regarding the adequacy of
the current standards. Studies that
examine health effect associations in
analyses that exclude the highest
exposures (i.e., studies that restrict
analyses below certain PM2.5
concentrations), and which report
positive and statistically significant
associations in analyses restricted to
annual average PM2.5 exposures at or
below 12 mg/m3 and/or to daily
exposures below 35 mg/m3 (section
II.B.3.b above and U.S. EPA, 2022b,
Table 3–10). The PA notes that these
restricted analyses provide additional
support for effects at lower
concentrations, exhibiting associations
for mean concentrations presumably
below the mean concentrations for the
main analyses. While mean PM2.5
concentrations for these restricted
analyses may not be reported in most
studies, the PA asserts that it would not
be unreasonable to presume that the
mean PM2.5 concentrations in the
restricted analyses are less than the
study-reported mean PM2.5
concentrations in the main analyses.
The two studies (Di et al., 2017b, and
Dominici et al., 2019) which report
means in their restricted analyses
(restricting annual average PM2.5
exposure below 12 mg/m3) and used
population-weighted approaches to
estimate PM2.5 exposures report mean
PM2.5 concentrations of 9.6 mg/m3.
However, it is important to note that,
even if the other studies had reported
the mean PM2.5 concentrations for the
restricted analysis, these means would
not necessarily have been useful in the
context of the decision framework as
was used in past reviews (above in
section II.B.3.b.), given uncertainties
associated with identifying the
relationship between a calculated mean
concentration that excludes specific
daily or annual average concentrations
above a certain threshold and the design
value used to determine compliance
with a standard (either the annual or 24hour standard). Moreover, the PA
emphasizes there is uncertainty in how
studies exclude concentrations (e.g., at
what spatial resolution are
concentrations being excluded), which
would make any comparisons of mean
concentrations in restricted analyses
difficult to compare to design values.
The PA also takes note of studies that
restrict 24-hour average PM2.5
concentrations to values of less than 35
mg/m3 and again recognizes that these
studies do not report the mean PM2.5
concentration for the restricted analysis,
as noted above, although the mean of
the restricted analysis is presumably
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less than the mean PM2.5 concentration
in the main analysis. However, in some
studies, the majority of PM2.5
concentrations from the main study are
already less than the restricted
concentration (e.g., in Di et al., 2017a,
where of all case and control days,
93.6% had PM2.5 concentrations below
25 mg/m3), which contributes to the
uncertainty in how much lower a mean
concentration in a restricted study is
compared to the mean PM2.5
concentration in the main analysis. As
a result, the PA recognizes that there are
limitations in how this information can
be used in evaluating the adequacy of
the current or potential alternative
levels of the 24-hour standard.
Additionally, the PA further recognizes
that it is difficult to use the means,
when reported, from studies of
restricted analyses to evaluate the level
of protection afforded by the current or
potential alternative levels of the
primary 24-hour PM2.5 standard because
the relationship between the studyreported mean concentration and the
98th percentile form of the 24-hour
standard is not well understood, in
particular for a short-term standard
designed to limit exposures to peak
PM2.5 concentrations.
Finally, the PA notes the availability
of accountability studies, which
evaluate whether environmental
policies or air quality interventions led
to changes in air quality and are also
associated with improvements in public
health, including a number of recent
studies evaluated in the ISA
Supplement (summarized above in
section II.B.3.b and U.S. EPA, 2022b,
Table 3–12). These studies report
positive and significant associations,
including some studies with annual
PM2.5 concentrations below 12.0 mg/m3
at the start of the study period,
indicating that public health
improvements may occur following
PM2.5 reductions in areas that already
meet the current annual PM2.5 standard.
For example, the PA notes that the
studies by Corrigan et al. (2018) and
Sanders et al. (2020a) and both found
improvements in mortality rates due to
improvements in air quality in both
attainment and nonattainment areas
following implementation of the 1997
primary annual PM2.5 NAAQS.
Additionally, the PA notes that an
accountability study by Henneman et al.
(2019a) evaluated the changes in
modeled PM2.5 concentrations following
the retirement of coal fired power plants
in the U.S found that reductions in
PM2.5 concentrations resulted in
reductions of cardiovascular-related
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hospital admissions.93 Other recent
studies additionally report that declines
in ambient PM2.5 concentrations over a
period of years have been associated
with decreases in mortality rates and
increases in life expectancy,
improvements in respiratory
development, and decreased incidence
of respiratory disease in children,
further supporting the robustness of
PM2.5 health effect associations reported
in the epidemiologic evidence.
In considering the available scientific
evidence, the PA recognizes that there
are a number of uncertainties associated
with the evidence that persist from
previous reviews. The PA notes that, for
controlled human exposures studies,
there are uncertainties related to
inconsistent results observed at
concentrations near ambient PM2.5
levels. Additionally, the PA recognizes
that it is unclear how the results of
controlled human exposure studies
alone and the importance of the effects
observed in these studies, particularly
in studies conducted at near-ambient
PM2.5 concentrations, should be
interpreted with respect to adversity to
public health. With respect to animal
toxicological studies, the PA notes that
while these studies also help establish
biological plausibility, uncertainty
exists in extrapolating the effects
observed in animal toxicological
studies, and the PM2.5 concentrations
that cause those effects, to human
populations.
Furthermore, the PA recognizes that
uncertainties associated with the
epidemiologic evidence (e.g., the
potential for copollutant confounding
and exposure measurement error)
remain, although new studies evaluated
in the ISA Supplement employ
statistical methods such as alternative
methods for confounder control, to more
extensively account for confounders,
which are more robust to model
misspecification. With regard to
controlling for potential confounders in
particular, the PA notes that the key
epidemiologic studies use a wide array
of approaches to control for potential
confounders. Time-series studies
control for potential confounders that
vary over short time intervals (e.g.,
including temperature, humidity, dew
point temperature, and day of the week),
while cohort studies control for
community- and/or individual-level
confounders that vary spatially (e.g.,
including income, race, age, SES,
93 We note that the studies by Corrigan et al.
(2018) and Sanders et al. (2020a) report monitorbased average PM2.5 concentrations, and the study
by reports model-based average PM2.5
concentrations, and that these studies do not report
design values.
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smoking, body mass index, and annual
weather variables such as temperature
and humidity) (U.S. EPA, 2022b, Table
B–4). Sensitivity analyses indicate that
adding covariates to control for
potential confounders can either
increase or decrease the magnitude of
PM2.5 effect estimates, depending on the
covariate, and that none of the
covariates examined can fully explain
the association with mortality (e.g., Di et
al., 2017b, Figure S2 in Supplementary
Materials). Thus, while no individual
study adjusts for all potential
confounders, a broad range of
approaches have been adopted across
studies to examine confounding,
supporting the robustness of reported
associations. Available studies
additionally indicate that PM2.5 health
effect associations are robust across
various approaches to estimating PM2.5
exposures and across various exposure
windows. This includes recent studies
that estimate exposures using groundbased monitors alone and studies that
estimate exposures using data from
multiple sources (e.g., satellites, land
use information, modeling), in addition
to monitors. While none of these
approaches eliminates the potential for
exposure error in epidemiologic studies,
the PA concludes that such error does
not call into question the fundamental
findings of the broad body of PM2.5
epidemiologic evidence.
Additionally, the PA notes the
uncertainties associated with the studies
that examine the shapes of C–R
functions over the full distribution of
ambient PM2.5 concentrations have not
identified a threshold concentration,
below which associations no longer
exist (section II.B.4 above, U.S. EPA,
2019a, section 1.5.3; U.S. EPA, 2022a,
sections 2.2.3.1 and 2.2.3.2). While such
analyses are complicated by the
relatively sparse data available at the
lower end of the air quality distribution
(U.S. EPA, 2019a, section 1.5.3), the
evidence remains consistent in
supporting a no-threshold relationship,
and in supporting a linear relationship
for PM2.5 concentrations >8 mg/m3.
However, uncertainties remain about
the shape of the C–R curve at PM2.5
concentrations <8 mg/m3, with some
recent studies providing evidence for
either a sublinear, linear, or supralinear
relationship at these lower
concentrations.
While studies using hybrid modeling
methods have demonstrated reduced
exposure measurement error and
reduced uncertainty in the health effect
estimates, these methodologies have
inherent limitations and uncertainties,
as described in more detail above in
section II.B.3.b and in sections 2.3.3.1.5
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and 3.3.4 of the PA, and the
performance of the modeling
approaches depends on the availability
of monitoring data which varies by
location. Factors likely contributing to
poorer model performance often
coincide with relatively low ambient
PM2.5 concentrations, in areas where
predicted exposures are at a greater
distance to monitors, and under
conditions where the reliability and
availability of key datasets (e.g., air
quality modeling) are limited. Thus, the
PA concludes that the uncertainty in
hybrid model predictions becomes an
increasingly important consideration as
lower predicted concentrations are
considered.
In addition, the PA recognizes that
there are uncertainties and limitations
in the analysis evaluating the
comparison of estimated PM2.5
concentrations using hybrid modeling
surfaces and their relationship to design
values that should be considered
(section II.B.3.b above; U.S. EPA, 2022b,
section 2.3.3.2.4). While design values
in general are higher than estimated
PM2.5 concentrations using these two
hybrid modeling approaches (DI2019
and HA2020), the PA recognizes that
these are just two hybrid modeling
approaches to estimating PM2.5
concentrations and other models/
approaches/spatial scales may result in
somewhat different PM2.5
concentrations and relationships with
design values. The analysis evaluating
the relationship between two different
hybrid modeling surfaces and design
values estimates PM2.5 concentrations
by CBSAs, but not every health study
uses PM2.5 estimates at this spatial scale,
and spatial scales for exposure estimates
can vary by study (section I.D.5 above;
U.S. EPA, 2022b, section 2.3.3.2.4). The
analysis completed was a nationwide
analysis and ratios between design
values and mean concentrations are
based on national estimates. However,
not all health studies are national
studies (i.e., some studies are completed
in different regions of the country, like
the southeast or northeast) and ratios in
different parts of the country could be
higher or lower, depending on factors
like population, as well as the
proportion of rural versus urban areas.
This analysis used specific air quality
years (2000–2016) and the use of other
air quality years could result in higher
or lower ratios.
Regardless of whether an
epidemiologic study uses monitoring
data or a hybrid modeling approach
when estimating PM2.5 exposures, the
PA recognizes that it is challenging to
interpret the study-reported mean PM2.5
concentrations and how they compare
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to design values. This is particularly
true given the variability that exists
across the various approaches to
estimate exposure and to calculate the
study-reported mean. The PA also
acknowledges that these types of
challenges are also present in using
information from Canadian studies to
directly and quantitatively inform
questions on the level of the annual
standard given the difficulty of
interpreting what the Canadian study
means represent relative to U.S. design
values.
b. Risk-Based Considerations
As in previous reviews, consideration
of the scientific evidence in this
reconsideration is informed by results
from a quantitative analysis of risk. The
overarching PA consideration regarding
these results is whether they alter the
overall conclusions from previous
reviews regarding health risk associated
with exposure to PM2.5 in ambient air
and associated judgments on the
adequacy of public health protection
provided by the current primary PM2.5
standards. The risk assessment
conducted for this reconsideration
develops exposure and risk estimates for
populations in 47 urban study areas, as
well as subsets of those study areas
depending on which of the primary
PM2.5 standards is controlling in a given
study area. The primary analyses focus
on exposure and risk associated with air
quality that might occur in an area
under air quality conditions that just
meet the current and potential
alternative standards. These study areas
include nearly 60 million people ages
30 years or older and illustrate the
differences likely to occur across
various locations with such air quality
as a result of area-specific differences in
emissions, meteorological, and
population characteristics. While the
same conceptual air quality scenarios
are simulated in all study areas (i.e.,
conditions that just meet the existing or
alternate standards), source,
meteorological and population
characteristics in the study areas
contribute to variability in the estimated
magnitude of risk across study areas
(U.S. EPA, 2022b, section 3.6.2.1). In
this way, the 47 areas provide a variety
of examples of exposure patterns that
can be informative to the
Administrator’s consideration of
potential exposures and risks that may
be associated with air quality conditions
occurring under the current and
potential alternative PM2.5 standards.
In considering the risk assessment in
this reconsideration, the PA notes a
number of ways in which the current
analyses update and improve upon
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those available in previous reviews. As
an initial matter, the PA notes that,
consistent with the overall approach for
this reconsideration, the risk assessment
has a targeted scope that focuses on allcause or nonaccidental mortality
associated with long- and short-term
PM2.5 exposures (U.S. EPA, 2022b,
section 3.4.1.2). As noted in section
II.B.1 above, the evidence assessed in
the 2019 ISA and ISA Supplement
support a causal relationship between
long- and short-term PM2.5 exposures
and mortality. Concentration-response
functions used in the risk assessment
are from large, multicity U.S.
epidemiologic studies that evaluate the
relationship between PM2.5 exposures
and mortality and were identified using
criteria that take into account factors
such as study design, geographic
coverage, demographic populations, and
health endpoints (U.S. EPA, 2022b,
section 2.1).
The risk assessment also includes
updates and improvements to input data
and modeling approaches, summarized
in section II.C above and in section 3.4
of the PA (U.S. EPA, 2022b). As in
previous reviews, exposure and risk are
estimated from air quality scenarios
defined by the highest design value in
the study area, which is the monitor
location with the highest 3-year average
of the annual mean PM2.5 concentrations
(e.g., equal to 12.0 mg/m3 for the current
standard scenario) for the annual PM2.5
standard and with the highest 3-year
average of the 98th percentile 24-hour
PM2.5 concentrations (e.g., equal to 35
mg/m3 for the current standard scenario)
for the 24-hour PM2.5 standard. As
described in more detail in section II.C
above and in section 3.4 of the PA (U.S.
EPA, 2022b), air quality modeling was
used to simulate just meeting the
existing annual and 24-hour standards
of 12.0 mg/m3 and 35 mg/m3 and to just
meeting potential alternative annual and
24-hour standards of 10.0 mg/m3 and 30
mg/m3. In addition to the air quality
modeling approach, linear interpolation
and extrapolation were used to simulate
just meeting alternative annual
standards with levels of 11.0
(interpolated between 12.0 and 10.0 mg/
m3), 9.0 mg/m3, and 8.0 mg/m3 (both
extrapolated from 12.0 and 10.0 mg/m3)
in the subset of study areas controlled
by the annual standard.
In addition to the risk assessment
described above, the PA presents
quantitative analyses that also assess
long-term PM2.5-attributable exposure
and mortality risk, stratified by racial/
ethnic demographics. As described in
more detail in section II.B.2 above, the
evidence suggests that different racial
and ethnic groups, such as Black and
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Hispanic populations residing in the
study areas, have higher PM2.5
exposures than White and non-Hispanic
populations also residing in the study
areas, respectively, thus contributing to
increased risk of PM-related effects. Of
the available studies, Di et al. (2017b)
was identified as best characterizing
populations potentially at increased risk
of long-term exposure-attributable allcause mortality effects and provides
race- and ethnicity-stratified C–R
functions for ages 65 and over (U.S.
EPA, 2022b, section 3.4.1.6 and
Appendix C). Risk and exposure are
quantitatively assessed within racial
and ethnic minority populations of
older adults in the full set of 47 areas
and the subset of 30 areas controlled by
the annual PM2.5 standard. This
analysis, when considered alongside
estimates of risk across all populations
in the 47 study areas, can help to inform
conclusions on the annual primary
PM2.5 standards that would be requisite
to protect the public health of
demographic populations potentially at
increased risk of long-term PM2.5-related
mortality effects.
In considering the risk results, the PA
focuses first on estimates for the full set
of 47 urban study areas. The risk
assessment estimates that the current
primary PM2.5 standards could allow a
substantial number of deaths in the
U.S., with the large majority of those
deaths associated with long-term PM2.5
exposures. For example, when air
quality in the 47 study areas is adjusted
to just meet the current standards, the
risk assessment estimates about 41,000
to 45,000 deaths from all-cause
mortality in a single year (e.g., for longterm exposures; confidence intervals
range from about 30,000 to 59,000) (U.S.
EPA, 2022b, section 3.4.2.1). For the 30
study areas 94 where just meeting the
current standards is controlled by the
annual standard,95 long-term PM2.5
exposures are estimated to be associated
with as many as 39,000 (confidence
intervals range from about 26,000 to
51,000) deaths from all-cause mortality
in a single year (U.S. EPA, 2022b,
section 3.4.2.2). For the 11 study areas 96
94 These 30 areas controlled by the annual
standard under all scenarios evaluated include a
population of approximately 48 million adults aged
30–99, or about 75% of the population included in
the full set of 47 areas.
95 For these areas, the annual standard is the
‘‘controlling standard’’ because when air quality is
adjusted to simulate just meeting the current or
potential alternative annual standards, that air
quality also would meet the 24-hour standard being
evaluated.
96 These 11 areas controlled by the 24-hour
standard under all scenarios evaluated include a
population of approximately 10 million adults aged
30–99, or about 17% of the population included in
the full set of 47 areas.
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where just meeting the current
standards is controlled by the daily
standard,97 long-term PM2.5 exposures
are estimated to be associated with as
many as 2,600 (confidence intervals
ranging from 1,700 to 3,400) deaths in
a single year (U.S. EPA, 2022b, section
3.4.2.3). The risk assessment estimates
far fewer deaths in a single year for
short-term PM2.5 exposures as compared
to long-term PM2.5 exposures, across all
of the study area subsets (U.S. EPA,
2022b, section 3.6.2.2).
While the absolute numbers of
estimated deaths vary across exposure
durations, populations, and C–R
functions, the general magnitude of risk
estimates supports the potential for
significant public health impacts in
locations meeting the current primary
PM2.5 standards. This is particularly the
case given that the large majority of
PM2.5-associated deaths for air quality
just meeting the current standards are
estimated at annual average PM2.5
concentrations from about 10 to 12 mg/
m3. These annual average PM2.5
concentrations fall within the range of
long-term average concentrations over
which key epidemiologic studies
provide strong support for reported
positive and statistically significant
health effect associations (U.S. EPA,
2022b, section 3.6.2.2).
In the 47 urban study areas, when air
quality is simulated to just meet
alternative standards, the PA notes that
there are substantially larger risk
reductions associated with lowering the
annual standard than with lowering the
24-hour standard. Risks are estimated to
decrease by 13–17% when air quality is
adjusted to just meet an alternative
annual standard with a level of 10.0 mg/
m3 or by 1–2% when adjusted to just
meet an alternative 24-hour standard
with a level of 30 mg/m3 (U.S. EPA,
2022b, section 3.4.2.1). The percentage
decrease when just meeting an
alternative annual standard with a level
of 10.0 mg/m3 corresponds to
approximately 7,400 fewer deaths per
year (confidence intervals ranging from
about 4,100 to 9,800) attributable to
long-term PM2.5 exposures (U.S. EPA,
2022b, section 3.4.2.1).
In the 30 study areas where just
meeting the current and alternative
standards is controlled by the annual
standard, air quality adjusted to meet
alternative annual standards with lower
97 For these areas, the 24-hour standard is the
controlling standard because when air quality is
adjusted to simulate just meeting the current or
potential alternative 24-hour standards, that air
quality also would meet the annual standard being
evaluated. Some areas classified as being controlled
by the 24-hour standard also violate the annual
standard.
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levels is associated with reductions in
estimated all-cause mortality risk. These
reductions in risk for alternative annual
levels are as follows: 7–9% reduction
for an alternative annual level of 11.0
mg/m3, 15–19% reduction for a level of
10.0 mg/m3, 22–28% reduction for a
level of 9.0 mg/m3, and 30–37%
reduction for a level of 8.0 mg/m3 (U.S.
EPA, 2022b, section 3.4.2.2). For each of
these standards, most of the risk
remaining is estimated at annual
average PM2.5 concentrations that fall
somewhat below the alternative
standard levels (U.S. EPA, 2022b,
section 3.4.2.2).
In considering the at-risk analysis, the
PA notes that across all simulated air
quality for both the full set of 47 and the
subset of 30 study areas, Blacks
experience the highest average PM2.5
concentrations of the demographic
groups analyzed. Native Americans
experienced the lowest average PM2.5
concentrations, particularly in the full
set of 47 study areas. White, Hispanic,
and Asian populations were exposed to
similar average PM2.5 concentrations.
Additionally, as the levels of potential
alternative annual PM2.5 standards
decrease, there is comparatively less
disproportionate exposure between
demographic populations (U.S. EPA,
2022b, section 3.4.2.4).
The PA recognizes that the risk
estimates can provide additional
information beyond the exposure
information to inform our
understanding of potentially
disproportionate impacts, in this
instance by including demographicspecific information on baseline
incidence and the relationship between
exposure and health effect. Across all
air quality scenarios and demographic
groups evaluated, Black populations in
the study areas are associated with the
largest PM2.5-attributable mortality risk
rate per 100,000 people, while White
populations in the study areas are
associated with the smallest PM2.5attributative mortality risk rate (U.S.
EPA, 2022b, section 3.4.2.4, Figure 3–
20). Generally, as the levels of potential
alternative annual PM2.5 standards
decrease in the 30 areas controlled by
the annual standard, the average
reductions in PM2.5 concentration and
mortality risk rates increase across all
demographic populations (U.S. EPA,
2022b, section 3.4.2.4, Figure 3–21).
In comparing the reductions in
average national PM2.5 concentrations
and risk rates within each demographic
population, the average percent PM2.5
concentrations and risk reductions are
slightly greater in the Black population
than in the White population for each
alternative standard evaluated (11.0 mg/
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m3, 10.0 mg/m3, 9.0 mg/m3, and 8.0 mg/
m3), when shifting from the current
annual PM2.5 standard (12.0 mg/m3) in
the full set of 47 areas and the subset of
30 areas controlled by the annual
standard. Furthermore, the difference in
average percent risk reductions
increases slightly more in Blacks than in
Whites as the level of the potential
alternative annual standard decreases
(U.S. EPA, 2022b, section 3.4.2.4, Table
3–19 and Table 3–20).
The PA also recognizes that there are
several particularly important
uncertainties that affect the quantitative
estimates of risk rates and exposure in
the at-risk analysis and their
interpretation in the context of
considering the current primary PM2.5
standards. These include uncertainties
related to the modeling and adjustment
methods for simulating air quality
scenarios; the potential influence of
confounders on the relationship
between PM2.5 exposure and mortality;
and the interpretation of the shapes of
C–R functions, particularly at lower
concentrations. It is also important to
recognize the limited availability of
studies to inform the at-risk analysis. As
noted in section II.C above and in
section 3.4 of the PA, the at-risk analysis
included C–R functions from one study,
Di et al. (2017b), which reported
associations between long-term PM2.5
exposures and mortality, stratified by
race/ethnicity, in populations age 65
and older. Of the studies available from
the 2019 ISA, Di et al. (2017b) was
identified as best characterizing
potentially at-risk minority populations
across the U.S.98 While the at-risk
analyses provide additional insight on
the estimated exposures and risks for
certain demographic groups, it is not
clear how the results would vary if: (1)
analyses included populations that were
younger than 65 years old, (2) the
analyses were conducted areas that are
demographically different than the 47
study areas included in this analysis,
and (3) the air quality adjustments
reflected source-specific emissions
reduction strategies. Therefore, in light
of the limitations and uncertainties
associated with the at-risk analyses, the
results should be considered within the
context of the full risk assessment. The
uncertainties associated with the
quantitative risk assessment and at-risk
analyses are described in more detail in
the PA (U.S. EPA, 2022b, section 3.4.2.5
and Appendix C) and are summarized
in section II.C.2 above.
98 Additional details on concentration-response
function identification can be found in Appendix
C, section C.3.2 of the PA.
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In considering the public health
implications of the risk assessment, the
PA notes that the purpose for the study
areas is to illustrate circumstances that
may occur in areas that just meet the
current or potential alternative
standards, and not to estimate risk
associated with conditions occurring in
those specific locations currently. The
PA notes that some areas across the U.S.
have air quality for PM2.5 that is near or
above the existing standards. Risks
associated with air quality above the
current standards are not informative to
decisions about the adequacy of the
current standards. This is because the
risk assessment uses an approach to
adjust air quality to just meet the
current standards, which means that
areas that have air quality that is above
the current standards would be adjusted
to just meet the current standards such
that the evaluation of changes in risk
and risk remaining would be associated
with those areas meeting the current
standards. The same is true for air
quality adjusted to simulate just meeting
alternative standard levels as well.
Thus, the air quality and exposure
circumstances assessed in the study
areas in the risk assessment are
specifically designed to inform whether
the currently available information calls
into question the adequacy of the public
health protection afforded by the
current standards, as well as to provide
information regarding potential
alternative standard levels.
The risk estimates for the study areas
assessed in this reconsideration reflect
differences in exposure circumstances
among those areas and illustrate the
exposures and risks that might be
expected to occur in other areas with
such circumstances under air quality
conditions that just meet the current
standards or the alternative standards
assessed. Thus, the exposure and risk
estimates indicate the magnitude of
exposure and risk that might be
expected in many areas of the U.S. with
PM2.5 concentrations at or near the
current or alternative standards.
Although the methodologies and data
used to estimate risks in this
reconsideration differ in several ways
from what was used in the 2020 review,
the findings and considerations
summarized in the PA present a pattern
of exposure and risk that is generally
similar to that considered in the 2020
review, and indicate a level of
protection generally consistent with that
described in the 2020 PA.
The PA notes that the considerations
related to the potential public health
implications of the risk assessment and
at-risk analysis are important to
informing the Administrator’s proposed
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decisions regarding the public health
significance of the risk assessment
results. Specifically, the PA notes that
available evidence and information
suggests that both long- and short-term
PM2.5 exposures are associated with
adverse health effects, including more
severe effects such as mortality. In
addition, the PA further notes that such
effects impact large segments of the U.S.
population, including those populations
that may have other factors that
influence risk (i.e., lifestage, pre-existing
cardiovascular and respiratory diseases,
race/ethnicity), as well as disparities in
PM2.5 exposures and health risks based
on race and ethnicity (U.S. EPA, 2022b,
section 3.6.2.5). Therefore, the PA
recognizes that the air quality allowed
by the current primary PM2.5 standards
could be judged to be associated with
significant public health risk. The PA
also recognizes that such conclusions
also depend in part on public health
policy judgments that will weigh in the
Administrator’s decision in this
reconsideration with regard to the
adequacy of protection afforded by the
current standards. Such judgments that
are common to NAAQS decisions
include those related to public health
implications of effects of differing
severity. Such judgments also include
those concerning the public health
significance of effects at exposures for
which evidence is limited or lacking,
such as effects at lower concentrations
than those demonstrated in the key
epidemiologic studies and in those
population groups for which
population-specific information, such as
C–R functions, are not available from
the epidemiologic literature.
3. Administrator’s Proposed
Conclusions on the Primary PM2.5
Standards
This section summarizes the
Administrator’s considerations and
proposed conclusions related to the
adequacy of the current primary PM2.5
standards and presents his proposed
decision to revise the primary annual
PM2.5 standard and retain the primary
24-hour PM2.5 standard. In establishing
primary standards under the Act that
are ‘‘requisite’’ to protect public health
with an adequate margin of safety, the
Administrator is seeking to establish
standards that are neither more nor less
stringent than necessary for this
purpose. He recognizes that the
requirement to provide an adequate
margin of safety was intended to
address uncertainties associated with
inconclusive scientific and technical
information and to provide a reasonable
degree of protection against hazards that
research has not yet identified.
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However, the Act does not require that
primary standards be set at a zero-risk
level; rather, the NAAQS must be
sufficiently protective, but not more
stringent than necessary.
Given these requirements, the
Administrator’s final decision in this
reconsideration will be a public health
policy judgment drawing upon
scientific and technical information
examining the health effects of PM2.5
exposures, including how to consider
the range and magnitude of
uncertainties inherent in that
information. This public health policy
judgment will be based on an
interpretation of the scientific and
technical information that neither
overstates nor understates its strengths
and limitations, nor the appropriate
inferences to be drawn, and will be
informed by the Administrator’s
consideration of advice from the CASAC
and public comments received on this
proposal document.
a. Adequacy of the Current Primary
PM2.5 Standards
In considering whether the currently
available scientific evidence and
quantitative risk-based information
support or call into question the
adequacy of the public health protection
afforded by the current primary PM2.5
standards, and as is the case with
NAAQS reviews in general, the extent to
which the current primary PM2.5
standards are judged to be adequate will
depend on a variety of factors, including
science policy and public health policy
judgments to be made by the
Administrator on the strength and
uncertainties of the scientific evidence.
The factors relevant to judging the
adequacy of the standards also include
the interpretation of, and decisions as to
the weight to place on, different aspects
of the results of the risk assessment for
the study areas included and the
associated uncertainties. Thus, the
Administrator’s proposed conclusions
regarding the adequacy of the current
standards will depend in part on
judgments regarding aspects of the
evidence and risk estimates, and
judgments about the degree of
protection that is requisite to protect
public health with an adequate margin
of safety.
i. Proposed Conclusions on the
Adequacy of the Current Primary PM2.5
Standards
In reaching proposed conclusions on
the adequacy of the current primary
PM2.5 standards, the Administrator has
considered the scientific evidence,
including that assessed in the 2019 ISA
and the ISA Supplement. The
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Administrator has also considered the
quantitative estimates of risk developed
in this reconsideration, including
associated uncertainties and limitations,
and the extent to which they indicate
differing conclusions regarding the
magnitude of risk, as well as level of
protection from adverse effects,
associated with the current standards.
The Administrator has additionally
considered the key aspects of the
evidence and risk estimates emphasized
in establishing the current standards,
and the associated public health policy
judgments and judgments about the
uncertainties inherent in the scientific
evidence and quantitative analyses that
are integral to the proposed conclusions
on the adequacy of the current primary
PM2.5 standards.
First, as described above in section
II.A.2, the Administrator’s approach
recognizes that the current annual
standard (based on arithmetic mean
concentrations) and 24-hour standard
(based on 98th percentile
concentrations), together, are intended
to provide public health protection
against the full distribution of short- and
long-term PM2.5 exposures. In evaluating
the adequacy of the current standards,
the Administrator focuses on evaluating
the public health protection afforded by
the annual and 24-hour standards, taken
together, against adverse health effects
associated with long- or short-term
PM2.5 exposures. This approach
recognizes that changes in PM2.5 air
quality designed to meet either the
annual or the 24-hour standard would
likely result in changes to both longterm average and short-term peak PM2.5
concentrations.
In general, the Administrator
recognizes that the annual standard is
most effective at controlling exposures
to ‘‘typical’’ daily PM2.5 concentrations
that are experienced over the year,
while the 24-hour standard, with its
98th percentile form, is most effective at
limiting peak daily or 24-hour PM2.5
concentrations. In considering the
combined effects of these standards, the
Administrator recognizes that changes
in PM2.5 air quality designed to meet an
annual standard would likely result not
only in lower short- and long-term PM2.5
concentrations near the middle of the
air quality distribution, but also in fewer
and lower short-term peak PM2.5
concentrations. Additionally, changes
designed to meet a lower 24-hour
standard, with a 98th percentile form,
would most effectively result in fewer
and lower peak 24-hour PM2.5
concentrations, but also have an effect
on lowering the annual average PM2.5
concentrations. Thus, the Administrator
acknowledges the focus in evaluating
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the current primary standards is on the
protection provided by the combination
of the annual and 24-hour standards
against the distribution of both shortand long-term PM2.5 exposures.
The Administrator recognizes the
longstanding body of health evidence
supporting relationships between PM2.5
exposures (short- and long-term) and
mortality or serious morbidity effects.
The evidence available in this
reconsideration (i.e., that assessed in the
2019 ISA (U.S. EPA, 2019a) and ISA
Supplement (U.S. EPA, 2022a) and
summarized above in section II.B.1 and
section II.D.2.a reaffirms, and in some
cases strengthens, the conclusions from
the 2009 ISA regarding the health effects
of PM2.5 exposures (U.S. EPA, 2009a).
As noted above, epidemiologic studies
demonstrate generally positive, and
often statistically significant, PM2.5
health effect associations. Such studies
report associations between estimated
PM2.5 exposures and non-accidental,
cardiovascular, or respiratory mortality;
cardiovascular or respiratory
hospitalizations or emergency room
visits; and other mortality/morbidity
outcomes (e.g., lung cancer mortality or
incidence, asthma development). Recent
experimental evidence, as well as
evidence from panel studies,
strengthens support for potential
biological pathways through which
PM2.5 exposures could lead to the
serious effects reported in many
population-level epidemiologic studies,
including support for pathways that
could lead to cardiovascular,
respiratory, nervous system, and cancerrelated effects. The Administrator also
recognizes that the PA notes that while
the full body of health effects evidence
is considered in this reconsideration of
the PM NAAQS, the greatest emphasis
in the PA is placed on the health effects
for which the evidence has been judged
in the 2019 ISA to demonstrate a
‘‘causal’’ or ‘‘likely to be causal’’
relationship with PM2.5 exposures (i.e.,
mortality, cardiovascular effects,
respiratory effects, cancer, and nervous
system effects). In considering the
available scientific evidence, consistent
with approaches employed in past
NAAQS reviews, the Administrator
places the most weight on evidence
supporting ‘‘causal’’ or ‘‘likely to be
causal’’ relationship with long or shortterm PM2.5 exposures. In addition, the
Administrator also takes note of those
populations identified to be at greater
risk of PM2.5-related health effects, as
characterized in the 2019 ISA and ISA
Supplement, and the potential public
health implications.
In evaluating the public health
protection afforded by the current
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primary PM2.5 standards against longand short-term PM2.5 exposures, the
Administrator considers the four basic
elements of the NAAQS (indicator,
averaging time, form, and level)
collectively. With respect to indicator,
the Administrator recognizes that the
scientific evidence in this
reconsideration, as in previous reviews,
continues to provide strong support for
health effects associated with PM2.5
mass. He notes the PA conclusion that
the available information continues to
support the PM2.5 mass-based indicator
and remains too limited to support a
distinct standard for any specific PM2.5
component or group of components, and
too limited to support a distinct
standard for the ultrafine fraction (U.S.
EPA, 2022b, section 3.6.3.2.1). In its
advice on the adequacy of the current
primary PM2.5 standards, the CASAC
reached consensus that the PM2.5 massbased indicator should be retained,
without revision (Sheppard, 2022a, p. 2
of consensus letter). Thus, as in the
2020 review (85 FR 82715, December
18, 2020) and consistent with the advice
from the CASAC, the Administrator
proposes to conclude that it is
appropriate to consider retaining PM2.5
mass as the indicator for the primary
standards for fine particles.
With respect to averaging time and
form, the Administrator notes that the
scientific evidence continues to provide
strong support for health effect
associations with both long-term (e.g.,
annual or multi-year) and short-term
(e.g., mostly 24-hour exposures to PM2.5)
(U.S. EPA, 2022b, section 3.6.3.2.2). In
this reconsideration, the epidemiologic
and controlled human exposure studies
have examined a variety of PM2.5
exposure durations. Epidemiologic
studies continue to provide strong
support for health effects associated
with short-term PM2.5 exposures based
on 24-hour PM2.5 averaging periods, and
the EPA notes that associations with
sub-daily estimates are less consistent
and, in some cases, smaller in
magnitude (U.S. EPA, 2019a, section
1.5.2.1; U.S. EPA, 2022b, section
3.6.3.2.2). In addition, controlled human
exposure and panel-based studies of
sub-daily exposures typically examine
subclinical effects rather than the more
serious population-level effects that
have been reported to be associated with
24-hour exposures (e.g., mortality,
hospitalizations). Taken together, the
2019 ISA concludes that epidemiologic
studies do not indicate that subdaily
averaging periods are more closely
associated with health effects than the
24-hour average exposure metric (U.S.
EPA, 2019a, section 1.5.2.1).
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Additionally, while recent controlled
human exposure studies provide
consistent evidence for cardiovascular
effects following PM2.5 exposures for
less than 24 hours (i.e., <30 minutes to
5 hours), exposure concentrations in
these studies are well-above the ambient
concentrations typically measured in
locations meeting the current standards
(U.S. EPA, 2022b, section 3.3.3.1).
Therefore, these studies do not provide
support for additional protection against
sub-daily PM2.5 exposures, beyond that
provided by the current primary
standards. In its advice on the adequacy
of the current primary PM2.5 standards,
the CASAC reached consensus that
averaging times for the standards should
be retained, without revision (Sheppard,
2022a, p. 2 of consensus letter). Thus, as
in the 2020 review (85 FR 82715,
December 18, 2020), and consistent with
the advice from the CASAC, the
Administrator reaches the proposed
conclusion that the currently available
evidence does not support considering
alternatives to the annual and 24-hour
averaging times for standards meant to
protect against long- and short-term
PM2.5 exposures.
With regard to form, the
Administrator proposes to conclude that
it is appropriate to consider retaining
the current form of both the annual and
the 24-hour standards. In so doing, he
first notes that, in the 1997 review, the
EPA set both an annual standard, to
provide protection from health effects
associated with both long- and shortterm exposures to PM2.5, and a 24-hour
standard to a supplement the protection
afforded by the annual standard (62 FR
38667, July 18, 1997). With regard to the
form of the annual standard, the
Administrator recognizes that a large
majority of the recently available
epidemiologic studies continue to report
associations between health effects and
annual average PM2.5 concentrations.
These studies of annual average PM2.5
concentrations provide support for
retaining the current form of the annual
standard to provide protection against
long- and short-term PM2.5 exposures. In
its advice on the adequacy of the current
standards, the CASAC reached
consensus that the form of the annual
standard (i.e., annual mean, averaged
over 3 years) should be retained,
without revision (Sheppard, 2022a, p. 2
of consensus letter). In relation to the
form of the 24-hour standard (98th
percentile, averaged over three years),
the Administrator notes that
epidemiologic studies continue to
provide strong support for health effect
associations with short-term (e.g.,
mostly 24-hour) PM2.5 exposures (U.S.
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EPA, 2022b, section 3.6.3.2.3) and that
controlled human exposure studies
provide evidence for health effects
following single short-term ‘‘peak’’
PM2.5 exposures. Thus, the evidence
supports retaining a standard focused
on providing supplemental protection
against short-term peak exposures and
supports a 98th percentile form for a 24hour standard. The Administrator
further notes that this form also
provides an appropriate balance
between limiting the occurrence of peak
24-hour PM2.5 concentrations and
identifying a stable target for risk
management programs (U.S. EPA,
2022b, section 3.6.3.2.3). While the
CASAC provided recommendations
regarding the adequacy of the current
24-hour standard conditional on the
current form (i.e., 98th percentile,
averaged over three years), they
recommended that in future reviews,
the EPA also consider alternative forms
for the primary 24-hour PM2.5 standard
(Sheppard, 2022a, p. 18 of consensus
responses). Furthermore, the
Administrator notes that the multi-year
percentile form (i.e., averaged over three
years) offers greater stability to the air
quality management process by
reducing the possibility that statistically
unusual indicator values will lead to
transient violations of the standard.
Thus, in considering the information
summarized above, and consistent with
the advice from the CASAC, the
Administrator reaches the preliminary
conclusion that it is appropriate to
consider retaining the forms of the
current annual and 24-hour PM2.5
standards. The Administrator solicits
public comment on the proposed
decision to retain the current form (98th
percentile, averaged over three years) of
the primary 24-hour PM2.5 standard. The
Administrator acknowledges that the
CASAC recommended retaining the
current form at this time but also
recommended that the EPA consider
alternatives to the current form in future
reviews. The EPA agrees that it would
be appropriate to gather additional air
quality and scientific information and
further consider these issues in future
reviews. This information will not be
utilized for this reconsideration process.
With regard to the level of the current
standards, the Administrator first
considers the scientific evidence
evaluated in the 2019 ISA and ISA
Supplement, and considerations
regarding the evidence as presented in
the PA. The Administrator recognizes
that the PA places greater weight on
epidemiologic studies conducted in the
U.S. and Canada, as these studies are
more directly applicable for quantitative
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considerations compared to studies
conducted in other countries. Studies
conducted in other countries outside of
the U.S. and Canada generally reflect
different populations, exposure
characteristics, air pollution mixtures,
and higher PM2.5 concentrations in
ambient air than are currently found in
the U.S. Therefore, consistent with
approaches in previous reviews, the
Administrator judges that it is
appropriate to place greater weight on
the U.S. and Canadian epidemiologic
studies in reaching conclusions
regarding the adequacy of the current
standards. In so doing, the
Administrator notes that the
epidemiologic studies in the U.S. and
Canada report health effect associations
with mortality and/or morbidity across
multiple cities and in diverse
populations, including in studies
examining populations and lifestages
that may be at increased risk of
experiencing a PM2.5-related health
effect (e.g., older adults, children,
populations with pre-existing
cardiovascular and respiratory disease,
minority populations, and low SES
communities). Further, he notes the
epidemiologic studies that use a variety
of statistical designs and employ a
variety of methods to examine exposure
measurement error as well as to control
for confounding effects, and he
acknowledges that results of these
analyses support the robustness of the
reported associations. Additionally, the
Administrator notes findings from an
expanded body of studies that employ
alternative methods for confounder
control and accountability methods
further inform the causal nature of the
relationship between long or short-term
term PM2.5 exposure and mortality as
described in the 2019 ISA and ISA
Supplement (U.S. EPA, 2019, sections
11.1.2.1, 11.2.2.4; U.S. EPA, 2022a,
sections 3.1.1.3, 3.1.2.3, 3.2.1.3, and
3.2.2.3). These studies, summarized
above in II.B.3 above and in Table 3–11
and Table 3–12 of the PA (U.S. EPA,
2022b) examine both short- and longterm PM2.5 exposure and cardiovascular
effects and mortality, and, using a
variety of statistical methods to control
for confounding bias, consistently report
positive associations, which further
supports the broader body of
epidemiologic evidence for both
cardiovascular effects and mortality.
Moreover, the Administrator notes that
recent epidemiologic studies strengthen
support for health effect associations at
PM2.5 concentrations lower than in
those evaluated in epidemiologic
studies available at the time of previous
reviews. Lastly, the Administrator notes
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that studies that examine the shape of
the C–R relationship over the full
distribution of ambient PM2.5
concentrations have not identified a
threshold concentration, below which
associations no longer exist (U.S. EPA,
2019a, section 1.5.3; U.S. EPA, 2022a,
sections 2.1.1.5.1 and 2.1.1.5.2).
However, the Administrator also notes
that uncertainties remain about the
shape of the C–R curve at PM2.5
concentrations <8 mg/m3, with some
recent studies providing evidence for
either a sublinear, linear, or supralinear
relationship at these lower
concentrations (section II.B.4 above;
U.S. EPA, 2019a, section 11.2.4; U.S.
EPA, 2022a, section 2.2.3.2).
In considering the available scientific
evidence to inform proposed decisions
on the adequacy of the current level of
the annual standard, the Administrator
acknowledges that the evidence
available in this reconsideration
provides support for adverse health
effect associations at lower ambient
PM2.5 concentrations than in previous
reviews. The Administrator notes that in
previous reviews (including 1997, 2006
and 2012 reviews), evidence-based
approaches focused on identifying
standard levels near or somewhat below
long-term mean concentrations reported
in key epidemiologic studies. These
approaches were supported by the
CASAC in previous reviews and are
supported in this reconsideration by the
current CASAC, who also referenced the
potential for considering other lines of
epidemiologic evidence.99 The
Administrator notes that in this
reconsideration, a large number of key
U.S. epidemiologic studies report
positive and statistically significant
associations for air quality distributions
with overall mean PM2.5 concentrations
that are well below the current level of
the annual standard of 12 mg/m3 (i.e.,
Figure 1 and Figure 2 above with
concentrations ranging down as low as
9.9 mg/m3 in U.S.-based monitor-based
studies and 9.3 mg/m3 in U.S.-based
hybrid model-based studies). The
Administrator also recognizes that,
while Canadian studies can be more
difficult to directly compare to the
annual design value used to determine
in compliance in the U.S., the overall
mean PM2.5 concentrations from the key
Canadian epidemiologic studies are
99 The Administrator notes that some members of
the CASAC advised that ‘‘for the purpose of
informing the adequacy of the standards’’
(Sheppard, 2022a, p. 8 of consensus responses) that
the EPA in future reviews include evaluation of
other metrics, including the distribution of
concentrations reported in epidemiologic studies
and in analyses restricting concentrations to below
the current standard level.
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close to, though somewhat lower than,
those from the U.S. studies. The range
of monitor-based mean PM2.5
concentrations is from 6.9 mg/m3 to 13.3
mg/m3 while the range of mean PM2.5
concentrations in studies that use
hybrid modeling is 5.9 mg/m3 to 9.8 mg/
m3.
In assessing the adequacy of the
current annual standard, the
Administrator also examines additional
epidemiologic studies, consistent with
CASAC advice, that provide
supplementary information for
consideration in reaching conclusions
regarding the current annual standard.
These studies include analyses that
restrict annual average PM2.5
concentrations to values below level the
annual standard (described above in
section II.B.3.b and in Table 3–10 of the
PA) and the CASAC advised that ‘‘for
the purpose of informing the adequacy
of the standards’’ that the EPA evaluate
the means from these studies. In this
reconsideration, there are two key
studies available that restrict average
annual PM2.5 concentrations to less than
12 mg/m3 (Di et al., 2017a, and Dominici
et al., 2019). These restricted analyses
report positive and statistically
significant associations with all-cause
mortality and report mean PM2.5
concentrations of 9.6 mg/m3. Thus, these
two epidemiologic studies provide
support for positive and statistically
significant associations at lower mean
PM2.5 concentrations. The
Administrator does note that
uncertainties exist in these analyses
(described in more detail in sections
II.B.3.b and II.D.2.a above), including
uncertainty in how studies exclude
concentrations (e.g., at what spatial
resolution are concentrations being
excluded), which would make any
comparisons of concentrations in
restricted analyses difficult to compare
directly to design values.
In considering the available key U.S.
epidemiologic studies, the
Administrator also notes that CASAC
recommended looking at the
distribution of concentrations reported
in epidemiologic studies for purposes of
informing the adequacy of the standards
and notes that a small number of studies
report PM2.5 concentrations
corresponding to the 25th and 10th
percentiles of health data or exposure
estimates. He observes that in studies
that use monitors to estimate PM2.5
exposures, 25th percentiles of health
events correspond to PM2.5
concentrations (i.e., averaged over the
study period for each study city) at or
above 11.5 mg/m3 and 10th percentiles
of health events correspond to PM2.5
concentrations at or above 9.8 mg/m3
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(i.e., 25% and 10% of health events,
respectively, occur in study locations
with PM2.5 concentrations below these
values) (Figure 1 above and U.S. EPA,
2022b, Figure 3–8). The Administrator
further observes that of the key U.S.
epidemiologic studies that use hybrid
modeling approaches to estimate longterm PM2.5 exposures, the ambient PM2.5
concentrations corresponding to 25th
percentiles of estimated exposures are
9.1 mg/m3 (Figure 2 above and U.S. EPA,
2022b, Figure 3–14). In key U.S.
epidemiologic studies that use hybrid
modeling approaches to estimate shortterm PM2.5 exposures, the ambient
concentrations corresponding to 25th
percentiles of estimated exposures, or
health events, are 6.7 mg/m3 and the
ambient PM2.5 concentration
corresponding to that 10th percentile
range from 4.7 mg/m3 to 7.3 mg/m3
(Figure 2 above and U.S. EPA, 2022b,
Figure 3–14). While the Administrator
places less weight on the limited
number of studies that report these
lower quartiles of the air quality
distributions, he notes these
concentrations are generally below the
level of the annual standard of 12 mg/
m3.
In further assessing the adequacy of
the current annual standard, the
Administrator also evaluates what the
accountability studies may indicate
with respect to potential for
improvements in public health with
improvements in air quality. In so
doing, he takes note of three
accountability studies (Sanders et al.,
2020b; Corrigan et al., 2018; and
Henneman et al., 2019a) newly available
in this reconsideration with starting
concentrations at or below 12.0 mg/m3
that indicate positive and significant
associations with mortality and
morbidity and reductions in ambient
PM2.5 (described above in section
II.B.3.b and in Table 3–12 of the PA)
and notes that these studies suggest
public health improvements may occur
at concentrations below 12 mg/m3.
Thus, in considering the available
scientific evidence to inform proposed
decisions on the adequacy of the current
primary annual PM2.5 standard, the
Administrator recognizes that there is a
long-standing body of epidemiologic
evidence that provides support for
associations between PM2.5 exposures
and health effects across a distribution
of air quality that includes
concentrations near (i.e., at, above, and
below) the current standards. As such,
the Administrator recognizes that the
available scientific evidence, as assessed
in the 2019 ISA and ISA Supplement,
including the newly available
epidemiologic studies and the
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supplemental information from specific
types of epidemiologic studies, provides
a strong scientific foundation for
consideration of the adequacy of the
level of the current annual standard.
In considering the available scientific
evidence to inform proposed decisions
on the adequacy of the current 24-hour
standard, the Administrator finds that
there is less information available to
support decisions on the 24-hour
standard than that summarized above
for the annual standard. When looking
to the experimental studies, he notes
that controlled human exposure studies
provide evidence for health effects
following single, short-term exposures
to PM2.5 concentrations that are greater
than those typically present in ambient
air. In the controlled human exposure
studies, the Administrator observes that
results are inconsistent, particularly at
lower PM2.5 concentrations, but that
studies do report statistically significant
effects on one or more indicators of
cardiovascular function following 2hour exposures to PM2.5 concentrations
at and above 120 mg/m3 (and at and
above 149 mg/m3 for vascular
impairment, the effect shown to be most
consistent across studies). As noted in
the 2019 ISA, these studies are
important in establishing biological
plausibility for PM2.5 exposures causing
more serious health effects, such as
those seen in short-term exposure
epidemiologic studies. However, as
noted in the PA, the observed effects in
these controlled human exposures
studies are ones that signal an
intermediate effect in the body, likely
due to short-term exposure to PM2.5, and
which may provide support that more
adverse effects may be experienced
following longer exposure durations
and/or exposure to higher
concentrations but such intermediate
effects typically would not, by
themselves, be judged as adverse.
Additionally, he acknowledges, as noted
by the CASAC, that these controlled
human exposure studies generally do
not include populations with
substantially increased risk from
exposure to PM2.5, such as children,
older adults, or those with more severe
underlying illness. So, noting these
points and balancing these limitations
(i.e., that the health outcomes observed
in these controlled human exposure
studies are not clearly adverse and that
the studies generally do not include
those at increased risk from PM2.5
exposure), the Administrator examines
the air quality analyses, described in
more detail in section II.B.3.a above, to
assess whether during recent air quality
conditions, areas meeting the current
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standards would experience the
concentrations reported in these
controlled human exposure studies. He
observes that these air quality analyses
demonstrate that the PM2.5 exposures
shown to cause consistent effects in the
controlled human exposure studies are
well-above the ambient concentrations
typically measured in locations meeting
the current primary standards, thus
suggesting that the current primary
PM2.5 standards provide protection
against these ‘‘peak’’ concentrations. In
fact, at air quality monitoring sites
meeting the current primary PM2.5
standards (i.e., the 24-hour standard and
the annual standard), the 2-hour
concentrations generally remain below
10 mg/m3, and rarely exceed 30 mg/m3.
Two-hour concentrations are higher at
monitoring sites violating the current
standards, but generally remain below
16 mg/m3 and rarely exceed 80 mg/m3.
Based on this information, the
Administrator finds that the current
suite of standards maintains sub-daily
concentrations far below the current
concentrations in controlled human
exposure studies where consistent
effects have been observed, and notes
that while these studies generally do not
include the most at-risk individuals, the
exposure concentrations in these studies
also do not elicit adverse effects.
In addition, the Administrator also
notes that the majority of the CASAC
provide support for their advice to
revise the current daily standard by
pointing to ‘‘substantial epidemiologic
evidence from both morbidity and
mortality studies’’ which ‘‘includes
three U.S. air pollution studies with
analyses restricted to 24-hour
concentrations below 25 mg/m3’’
(Sheppard, 2022a, p. 17 consensus
responses). In considering this advice
from the majority of the CASAC, the
Administrator notes that the substantial
epidemiologic evidence available in this
reconsideration, including the studies
that restrict short-term (24-hour average
PM2.5 concentrations) PM2.5 exposures
below 25 mg/m3, provides support for
positive and statistically significant
associations between exposure to shortterm PM2.5 concentrations and all-cause
mortality (Di et al., 2017a) and CVD
hospital admissions (deSouza et al.,
2021, and Di et al., 2017a). In particular,
for the available epidemiologic studies
that employ restricted analyses of shortterm exposure studies, multicity studies
indicate that positive and statistically
significant associations with mortality
persist in analyses restricted to shortterm (24-hour average PM2.5
concentrations) PM2.5 exposures below
35 mg/m3 (Lee et al., 2015), below 30 mg/
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m3 (Shi et al., 2016), and below 25 mg/
m3 (Di et al., 2017a). Thus, the
Administrator agrees that these studies
help to provide additional support for
reaching conclusions on causality in the
2019 ISA. Additionally, when
considering these studies, the restricted
approach in these short-term studies
most clearly indicates that risks
associated with short-term PM2.5
exposures are not disproportionately
driven by the peaks of the air quality
distribution. While this is useful
information, it does not help to inform
questions on the adequacy of the current
24-hour standard given that the 24-hour
standard focuses on reducing ‘‘peak’’
exposures (with its 98th percentile
form). In further evaluating these
studies, the Administrator notes that the
fact that there are positive and
significant associations in these
analyses does not mean that one can
conclude that there would be short-term
effects occurring in areas that meet a 24hour standard at these levels. This is
true for multiple reasons. First, there are
uncertainties with respect to the
methodologies used in these studies to
exclude concentrations and the specific
methodology used (e.g., are individual
days with concentrations above the
concentration of interest in the
restricted analyses excluded at the
modeled grid cell level or the ZIP code
level rather than removing entire areas
with day(s) that exceed that
concentration) has direct implications
for the resulting air quality scenario(s).
This in turn affects how the adjusted air
quality scenarios in these studies can be
related to air quality distributions and
exposures to PM2.5 concentrations in
ambient air and thus how the data can
be interpreted with regard to the current
standard level. Second, given that these
studies are only evaluating daily or
annual average PM2.5 concentrations
that would correspond to the levels of
the standards, they do not consider
these levels along with the forms and
averaging times of the standards. This is
quite limiting for use in judging the
adequacy of the 24-hour standard given
that the study-reported mean
concentration is not useful in informing
the level of a standard with a 98th
percentile form that is designed to limit
exposures to peak PM2.5 concentrations.
Further, as noted in the PA, the studyreported means from these studies, are
not useful in identifying a level at
which we can say with some confidence
that effects are occurring due to impacts
from ‘‘peak’’ exposures (i.e., those most
closely aligned with the protection
provide by the 24-hour standard, with
its 98th percentile form) but are instead
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more useful in informing questions
about impacts from ‘‘typical’’ or average
24-hour exposures (i.e., those most
closely aligned with the protection
provided by the annual standard). These
uncertainties and lack of information
available from these studies are quite
limiting and as such, the Administrator
concludes that it is unclear how to
apply these studies to a decision
framework that could inform whether
the level of the current 24-hour standard
is or is not adequate. However, the
Administrator notes this uncertainty
may not be quite as limiting for using
restricted analyses studies to inform
conclusions regarding the adequacy of
the annual standard, given that the
study-reported means could be
evaluated in the context of the decision
framework described above for
informing proposed decisions on the
level of the annual standard. However,
in considering the available evidence
with regard to the current 24-hour PM2.5
standard, while the Administrator
agrees with the majority of the CASAC’s
comment that the controlled human
exposure studies have significant
limitations which must be considered
when reaching conclusions on the
adequacy of the current 24-hour
standard, he finds that restricted
analyses studies have significant
limitations and do not provide a
stronger line of evidence with which to
inform his proposed decisions on the
current 24-hour standard.
In addition to the evidence above, the
Administrator also considers what the
risk assessment indicates with regard to
the adequacy of the current primary
annual and 24-hour PM2.5 standards.
These analyses provide estimates of
PM2.5-attributable mortality which are
estimated based on input data that
include C–R functions from
epidemiologic studies that have no
threshold and a linear C–R relationship
down to zero, as well an air quality
adjustment approach that incorporates
proportional decreases in PM2.5
concentrations to meet lower standard
levels. The Administrator observes that
the risk assessment estimates that the
current primary annual PM2.5 standard
could allow a substantial number of
deaths in the U.S. For example, when
air quality in 30 study areas is adjusted
to simulate just meeting the current
annual standard, the risk assessment
estimates long-term PM2.5 exposures to
be associated with as many as 39,000
total deaths, with confidence intervals
ranging from 26,000–51,000. The
Administrator notes that these estimates
do not reflect uncertainties in
associations of health effects at lower
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concentrations and simulated air quality
improvements will always lead to
proportional decreases in risk (i.e., each
additional mg/m3 reduction produces
additional benefits with no clear
stopping point). Noting these limitations
and noting that the absolute numbers of
estimated deaths vary across exposure
durations, populations, and C–R
functions, he also observes that the
general magnitude of risk estimates
supports the potential for significant
public health impacts in locations
meeting the current primary annual
PM2.5 standard. He observes that this is
particularly the case given that the large
majority of PM2.5-associated deaths for
air quality just meeting the current
annual standard are estimated at annual
average PM2.5 concentrations from about
10 to 12 mg/m3, annual average PM2.5
concentrations that fall well within the
range of long-term average
concentrations over which key
epidemiologic studies provide strong
support for reported positive and
statistically significant PM2.5 health
effect associations. With respect to the
CASAC’s advice on the risk assessment,
the Administrator notes that the
majority of the CASAC agreed that
‘‘[t]he results support the conclusion
that the current primary annual PM2.5
standard does not adequately protect
public health’’ (Sheppard, 2022a, p. 2 of
consensus letter) and that ‘‘[t]he CASAC
concurs with the EPA’s assessment that
meaningful risk reductions will result
from lowering the annual PM2.5
standard’’ (Sheppard, 2022a, p. 3 of
consensus letter). Additionally, the
minority of CASAC also agreed that the
risk assessment results support revision
to the annual standard but commented
that there were important uncertainties
in the analyses and interpretation of the
analyses for annual standard levels
below 10 mg/m3 (Sheppard, 2022a, p. 3
of consensus letter).
The Administrator also recognizes
that the risk assessment was able to
include a new analysis based on the
availability of a new study in this
reconsideration that provided mortality
risk coefficients for older adults (i.e., 65
years and older) based on PM2.5
exposure and stratified by racial and
ethnic demographics. This at-risk
analysis provided estimates of potential
long-term PM2.5-attributable exposure
and mortality risk in older adults,
stratified by racial/ethnic demographics,
when meeting a revised annual standard
with a lower level. The Administrator
recognizes that this analysis is subject to
the same uncertainties as those
associated with the main risk
assessment estimates, including being
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limited to a subset of areas across the
U.S. and influenced by air quality
adjustment methodologies that may not
produce estimates of PM2.5
concentration exposures that match
those that can result from control
strategies implemented to meet more
stringent standards, and that the results
are based on the risk coefficients of only
one epidemiologic study. Taking into
account these uncertainties and
limitations, he does judge that the
analysis supports that a lower annual
standard level (i.e., below 12 mg/m3 and
down as low as 8 mg/m3) will help to
reduce PM2.5 exposure and may also
help to mitigate risk disparities. The
Administrator notes that what urban
areas are included in the risk
assessment analysis will greatly
influence the results but notes that
based on the areas included in the
analyses, the results show the largest
impact is on reducing exposure and risk
in Black populations, who were
estimated in the risk assessment case
study areas to have the highest levels of
exposures and the greatest rates of
premature mortality risk.
With respect to the 24-hour standard,
the risk assessment indicates that the
annual standard is the controlling
standard across most of the urban study
areas evaluated. When air quality is
adjusted to just meet an alternative 24hour standard level of 30 mg/m3 in the
areas where the 24-hour standard is
controlling, the risk assessment
estimates reductions in PM2.5-associated
risks across a more limited population
and number of areas compared to when
air quality is adjusted to simulate
alternative levels for the annual
standard, and these predictions are
largely confined to areas located in the
western U.S., several of which are also
likely to experience risk reductions
upon meeting a revised annual
standard. With respect to CASAC
advice, the Administrator notes that the
minority of CASAC advised that these
results suggest that the annual standard
can be used to limit both long- and
short-term PM2.5 concentrations and
views these risk assessment results as
supporting the conclusion that the
current 24-hour standard is adequate
(Sheppard, 2022a, p. 4 of consensus
letter). In contrast, the majority of
CASAC members commented that they
placed greater weight on the evidencebased considerations than on the values
estimated by the risk assessment, noting
the potential for uncertainties in how
the risk assessment was able to ‘‘capture
areas with wintertime stagnation and
residential wood-burning where the
annual standard is less likely to be
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protective’’ (Sheppard, 2022a, p. 4 of
consensus letter). The majority of the
CASAC members further state that
‘‘[t]here is also less confidence that the
annual standard could adequately
protect against health effects of shortterm exposures. A range of 25–30 mg/m3
for the 24-hour PM2.5 standard would be
adequately protective’’ (Sheppard,
2022a, p. 4 of consensus letter). The
majority of the CASAC members further
state that ‘‘[t]here is also less confidence
that the annual standard could
adequately protect against health effects
of short-term exposures. A range of 25–
30 mg/m3 for the 24-hour PM2.5 standard
would be adequately protective’’
(Sheppard, 2022a, p.4 of consensus
letter).
In considering the application of the
risk assessment in a decision framework
assessing the adequacy of the current
24-hour standard, the Administrator
again notes that the risk assessment
analyses of PM2.5-attributable mortality
use input data that include C–R
functions from epidemiologic studies
that have no threshold and a linear C–
R relationship down to zero, as well an
air quality adjustment approach that
incorporates proportional decreases in
PM2.5 concentrations to meet lower
standard levels, and that this
quantitative approach does not
incorporate any elements of uncertainty
in associations of health effects at lower
concentrations and simulated air quality
improvements will always lead to
proportional decreases in risk (i.e., each
additional mg/m3 reduction produces
additional benefits with no clear
stopping point). Therefore, the
Administrator recognizes that the risk
estimates can help to place the evidence
for specific health effects into a broader
public health context but should be
considered along with the inherent
uncertainties and limitations of such
analyses when informing judgments
about the potential for additional public
health protection associated with PM2.5
exposure and related health effects. The
Administrator also notes that in the
U.S., current air quality shows that the
24-hour standard is controlling in very
few areas and thus, it is understandable
that there are very few areas that would
be included in the study areas in the
risk assessment. The Administrator also
recognizes that the risk assessment did
not provide quantitative information on
risk impacts associated with an
alternative 24-hour standard level of 25
mg/m3.
Based on the above considerations,
the Administrator reaches the proposed
conclusion that the available scientific
evidence (summarized above in section
II.B) and quantitative risk assessment
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(summarized above in section II.C), can
reasonably be viewed as calling into
question the adequacy of the public
health protection afforded by the
current annual standard. In reaching
this conclusion, the Administrator
places weight on the extensive
epidemiologic evidence available in this
reconsideration, strengthened from
previous reviews, showing associations
between adverse health effects
(particularly cardiovascular effects and
mortality) and long-term mean PM2.5
concentrations, and notes the number
and strength of studies available
showing associations with mean PM2.5
concentrations well below the current
annual standard of 12.0 mg/m3. The
Administrator also takes note of the
evidence supporting the biological
plausibility of these associations,
including toxicological studies and
controlled human exposure studies.
When turning to additional information
from the epidemiologic evidence base,
he notes the advice from CASAC to also
consider the 25th percentile of the data
that is available and the study reported
means from long-term studies that
restrict concentrations to below 12 mg/
m3. When considering the 25th
percentile of the data, the Administrator
notes that it is available from a limited
number of epidemiologic studies and
that the current level of the annual
standard is above most of the 25th
percentile values reported in the key
epidemiologic studies. When looking to
the restricted analyses studies, he notes
that there are two studies that report
positive and statistically significant
associations with all-cause mortality,
and report a study mean PM2.5
concentration of 9.6 mg/m3. While
noting the limited nature of these two
lines of evidence and the associated
uncertainties, the Administrator does
judge that these data support the need
to revise the annual standard level.
Lastly, with respect to the
epidemiologic evidence, the
Administrator also takes into account
accountability studies newly available
in this reconsideration with starting
concentrations at or below 12.0 mg/m3
that indicate positive and significant
associations with mortality and
morbidity and reductions in ambient
PM2.5 and notes that these studies
suggest public health improvements
may occur at concentrations below 12
mg/m3.
The Administrator also considers the
results of the risk assessment in light of
the information it provides on risks
associated with the current and more
stringent levels of the annual standard.
While he recognizes a number of
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uncertainties and limitations associated
with the quantitative estimates of the
risk assessment, he judges that the
estimated risks remaining under air
quality adjusted to just meet the current
suite of standards are too high to be
considered requisite to protect public
health with an adequate margin of
safety, noting in particular the large
number of premature deaths estimated
to remain with air quality that just
meets the current annual standard. The
Administrator also recognizes that the
risk assessment was able to include a
new analysis (at-risk analysis) that
provided estimates of potential longterm PM2.5-attributable exposure and
mortality risk in older adults, stratified
by racial/ethnic demographics, when
meeting a revised annual standard with
a lower level. While the Administrator
recognizes that this analysis is subject to
multiple uncertainties and limitations
(as noted above in sections II.C.2 and
II.D.2.b), he does judge that the analysis
suggests that a lower annual standard
level (i.e., below 12 mg/m3 and down as
low as 8 mg/m3) will help to reduce
PM2.5 exposure and may also help to
mitigate exposure and risk disparities.
Finally, the Administrator considers the
advice from the CASAC, who
unanimously recommended revising the
annual standard.
The Administrator finds it is less clear
whether the available scientific
evidence and quantitative information
call into question the adequacy of the
public health protection afforded by the
current 24-hour standard, particularly
when considered in conjunction with
the protection provided by the suite of
standards and the proposed decision to
revise the annual standard. In
considering the scientific evidence, he
notes that the controlled human
exposure studies do not provide a
threshold below which no effects occur
and they do not include the most at-risk
populations. However, the
concentrations reported in these studies
are for observed effects that signal a
change in the body likely due to shortterm exposure to PM2.5 and which may
be the prelude to more adverse effects
following longer duration and/or higher
concentration exposures but typically
would not, by themselves, be judged as
adverse. Balancing this with the
observation that the air quality
concentrations in areas meeting the
current standards are well below the
PM2.5 concentrations shown to elicit
effects in these studies, the
Administrator does not judge that these
studies call into question the adequacy
of the current 24-hour standard. With
respect to the epidemiologic evidence,
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the Administrator notes that the body of
epidemiologic evidence provides
limited support for judging adequacy of
the level of the 24-hour standard. As
discussed in detail above (section
II.B.3.b), epidemiologic studies provide
the strongest support for reported health
effect associations for the part of the air
quality distribution corresponding to
the bulk of the underlying data (i.e.,
estimated exposures and/or health
events), often around the overall mean
concentrations evaluated rather than
near the upper end of the distribution.
While there are three studies available
in this reconsideration that restricted
24-hour concentrations to
concentrations below 25 mg/m3 and
while some members of CASAC pointed
to these studies as the basis for their
recommendation to revise the 24-hour
standard, the Administrator
preliminarily concludes that the results
from these studies, particularly in light
of the uncertainties associated with
these studies (as discussed above), are
an inadequate basis for revising the
level of the 24-hour PM2.5 standard.
When evaluating the risk assessment
information, the Administrator notes
that the risk assessment estimates a
reduction of 9–13% PM2.5 attributable
mortality in areas where the 24-hour
standard is controlling when the 24hour PM2.5 standard is reduced from a
level of 35 mg/m3 to 30 mg/m3. The
Administrator notes that this estimated
reduction in PM2.5-associated risks is
across a more limited population and is
largely confined to a small number of
areas located in the western U.S. Other
areas included in the risk assessment
were shown to experience risk
reductions that were driven primarily
by meeting a lower annual standard
level (though the associated change in
air quality also resulted in lower 24hour standard concentrations). With
respect to CASAC advice, the
Administrator notes that the majority of
CASAC advised that less weight be
placed, while the minority of CASAC
advised that these risk assessment
results support the conclusion that the
current 24-hour standard is adequate
(Sheppard, 2022a, p. 4 of consensus
letter), the majority of CASAC advised
that less weight be placed on the risk
assessment results and noted the
potential for uncertainties in how the
risk assessment was able to ‘‘capture
areas with wintertime stagnation and
residential wood-burning where the
annual standard is less likely to be
protective’’ (Sheppard, 2022a, p. 4 of
consensus letter).
Based on the current evidence and
quantitative information, as well as
consideration of CASAC advice and
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public comment thus far in this
reconsideration, the Administrator
proposes to conclude that the current
primary PM2.5 standards are not
adequate to protect public health with
an adequate margin of safety. While he
notes that the scientific evidence and
quantitative information clearly call into
question the adequacy of the public
health protection afforded by the
current annual standard, the
Administrator finds it is less clear
whether the available scientific
evidence and quantitative information
calls into question the adequacy of the
public health protection afforded by the
current 24-hour standard. In considering
how to revise the suite of standards to
provide the requisite degree of
protection, he recognizes that changes
in PM2.5 air quality designed to meet
either the annual or the 24-hour
standard would likely result in changes
to both long-term average and shortterm peak PM2.5 concentrations. He also
recognizes that the current annual
standard and 24-hour standard,
together, are intended to provide public
health protection against the full
distribution of short- and long-term
PM2.5 exposures. As noted above, the
annual standard is targeted at
controlling the typical exposures for
which the evidence of adverse health
effects is strongest. The Administrator
places the most weight on the large
number and strength of epidemiologic
studies that report positive, and often
statistically significant, associations
with long-term mean reported PM2.5
concentrations well below the current
level of the annual standard of 12.0 mg/
m3, as well as corroborating evidence
from U.S. accountability studies with
starting concentrations below 12 mg/m3
and studies that found positive and
statistically significant associations in
analyses restricted to concentrations
less than 12 mg/m3. In considering the
risk assessment information, he notes
that, for most of the U.S., the annual
standard is the controlling standard and
that the risk assessment estimates
reductions in PM2.5-associated risks
across more of the population and in
more areas with alternative annual
standard levels compared to estimates
for alternative 24-hour standard levels.
Moreover, the Administrator notes that
a more stringent annual standard has
been shown to effectively reduce both
average (annual) concentrations and
peak (daily) concentrations, ensuring
the broadest protection of public health.
Finally, the Administrator notes that the
CASAC was unanimous in its advice
regarding the need to revise the annual
standard, although they did not reach
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consensus on what range of alternative
levels would be most appropriate to
consider. Thus, in considering how to
revise the suite of standards to provide
the requisite degree of protection, the
Administrator proposes to conclude it is
appropriate to focus on revising the
annual standard.
b. Consideration of Alternative Primary
Annual PM2.5 Standard Levels
This section summarizes the
Administrator’s conclusions and
proposed decisions related to the
current primary annual PM2.5 standard
and presents his proposed decision to
revise the level of the current annual
standard within the range of 9.0 to 10.0
mg/m3, in conjunction with retaining the
current indicator, averaging time, and
form of that standard. The EPA is also
soliciting public comment on alternative
annual standard levels down to 8.0 mg/
m3 and up to 11.0 mg/m3, on an
alternative 24-hour standard level as
low as 25 mg/m3 and on the combination
of annual and 24-hour standards that
commenters may believe is appropriate,
along with the approaches and
rationales used to support such levels.
In establishing primary standards
under the Act that are ‘‘requisite’’ to
protect public health with an adequate
margin of safety, the Administrator is
seeking to establish standards that are
neither more nor less stringent than
necessary for this purpose. He
recognizes that the requirement to
provide an adequate margin of safety
was intended to address uncertainties
associated with inconclusive scientific
and technical information and to
provide a reasonable degree of
protection against hazards that research
has not yet identified. However, the Act
does not require that primary standards
be set at a zero-risk level; rather, the
NAAQS must be sufficiently protective,
but not more stringent than necessary.
Having reached the conclusion that
the current indicator, averaging time,
and form of the standard are appropriate
for the reasons outlined above, the
Administrator next considers the range
of potential alternative standard levels
that could be reasonably supported by
the available scientific evidence and
risk-based information to increase
public health protection against shortterm and long-term PM2.5 exposures.
The evidence available in this
reconsideration regarding PM2.5
exposures associated with health effects
affirms and strengthens the evidence
available at the completion of the 2009
ISA, taking into account studies
evaluated in the 2019 ISA and ISA
Supplement. The Administrator
recognizes that the weight of evidence is
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strongest for health effects for which the
2019 ISA concludes that the evidence
provides support for a causal
relationship between PM2.5 exposures
and health effects, including those
between long- and short-term PM2.5
exposures and mortality and
cardiovascular effects. He recognizes
that the weight of evidence is also
strong for health effects for which the
2019 ISA concludes that the evidence
supports a likely to be causal
relationship, which include long- and
short-term PM2.5 exposures and
respiratory effects and long-term PM2.5
exposures and cancer, and nervous
system effects.
In considering the available scientific
evidence that could inform conclusions
regarding potential alternative levels of
the annual PM2.5 standard, the
Administrator notes that in past
reviews, the decision framework used to
judge adequacy of the existing PM2.5
standards, and what levels of any
potential alternative standards should
be considered, placed significant weight
on epidemiologic studies that assessed
associations between PM2.5 exposure
and health outcomes that were most
strongly supported by the body of
scientific evidence (i.e., causal or likely
to be causal determinations). In so
doing, the Administrator recognizes that
the number of epidemiologic studies has
expanded since the completion of the
2009 ISA and the epidemiologic studies
evaluated in the 2019 ISA and the ISA
Supplement continue to report positive
and statistically significant associations
between long- and short-term exposure
to PM2.5 and mortality and morbidity.
Additionally, the Administrator
recognizes that the available
epidemiologic studies enable the
examination of the entire population
and include, and even focus on, those
that may be at comparatively higher risk
of experiencing a PM2.5-related health
effects. The Administrator notes that the
2019 ISA found that factors that may
contribute to increased risk of PM2.5related health effects include lifestage
(children and older adults), pre-existing
diseases (cardiovascular disease and
respiratory disease), and SES, and that
the ISA Supplement noted new
evidence that further supported racial
and ethnic differences in PM2.5
exposures and PM2.5-related health
risks. The Administrator also observes
that at-risk populations make up a
substantial portion of the U.S.
population (section II.B.2 above),
including children (22%) and older
adults (16%), as well as non-Hispanic
Black (12%) and Hispanic populations
(18%) and that the prevalence of preexisting diseases varies by lifestage and
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race/ethnicity. The Administrator notes
that the cohorts examined in the
epidemiologic studies available in this
reconsideration include diverse
populations that are broadly
representative of the U.S. population as
a whole, and include those populations
identified as at-risk (i.e., children and
older adults), as well as individuals in
the general population with pre-existing
disease, such as cardiovascular disease
and respiratory disease.
Recent epidemiologic studies also
strengthen support for health effect
associations at lower ambient PM2.5
concentrations than previous reviews
and studies that examine the shapes of
C–R functions over the full distribution
of ambient PM2.5 concentrations have
not identified a threshold concentration,
below which associations no longer
exist (U.S. EPA, 2019a, section 1.5.3;
U.S. EPA, 2022a, sections 2.2.3.1 and
2.2.3.2). Though these analyses are
complicated by the relatively sparse
data available at the lower end of the air
quality distribution (U.S. EPA, 2019a,
section 1.5.3), the evidence remains
consistent in supporting a no-threshold
relationship, and in supporting a linear
relationship for PM2.5 concentrations >
8 mg/m3, though uncertainties remain
about the shape of the C–R curve at
PM2.5 concentrations < 8 mg/m3.
With respect to uncertainties in
epidemiologic studies, a broad range of
approaches have been adopted across
studies to examine confounding and the
results of those examinations support
the robustness of reported associations.
Additionally, there is a considerable
amount of new epidemiologic evidence
in this reconsideration, including a large
number of new epidemiologic studies
that use varying study designs that
reduce uncertainties, including studies
that employ alternative methods for
confounder control and support
associations between exposure and
adverse health effects at lower PM2.5
concentrations. Consistent findings from
the broad body of epidemiologic studies
are supported by studies employing
alternative methods for confounder
control, which used a variety of
statistical methods to control for
confounding bias and consistently
report positive associations. The results
of these studies support the positive and
significant effects seen in cohort studies
associated with short- and long-term
exposure to PM2.5 and mortality.
Moreover, epidemiologic studies
continue to evaluate the uncertainty
related to exposure measurement error,
and while none of these approaches
eliminates the potential for exposure
error in epidemiologic studies, the
consistent reporting of PM2.5 health
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effect associations across exposure
estimation approaches, even in the face
of exposure error, together with the
larger effect estimates reported in some
studies that have attempted to reduce
exposure error, provides further support
for the robustness of associations
between PM2.5 exposures and mortality
and morbidity. Therefore, given the
strength of the available epidemiologic
evidence, including the ability of these
studies to provide information about
impacts on the most at-risk populations,
the Administrator concludes that the
strongest available evidence for
evaluating alternative levels of the
annual standard continues to be the
epidemiologic studies.
The evidence base available in this
reconsideration also consists of
experimental studies that include
controlled human exposure studies and
animal toxicological studies. These
studies demonstrate health outcomes
following long-term and short-term
exposure to PM2.5 at exposures that are
well-above those typically found in
ambient air. This body of evidence
provides support for the biological
mechanisms and the plausibility of the
serious health effects associated with
ambient PM2.5 exposures in
epidemiologic studies. Thus, the
Administrator recognizes that while
experimental studies may not be as
useful in a decision-making framework
alone, results from these studies lend
further support to the use of the
epidemiologic evidence base in
informing the level of the annual
standard.
In considering the level of the annual
standard, the Administrator recognizes
that the annual standard, with its form
based on the arithmetic mean
concentration, is most appropriately
meant to limit the ‘‘typical’’ daily and
annual exposures that are most strongly
associated with the health effects
observed in epidemiologic studies.
However, the Administrator also
recognizes that while epidemiologic
studies examine associations between
distributions of PM2.5 air quality and
health outcomes, they do not identify
particular PM2.5 exposures that cause
effects. Thus, any approach that uses
epidemiologic information in reaching
decisions on what standards are
appropriate necessarily requires
judgments of the Administrator about
how to consider the information
available from the epidemiologic studies
as a basis for appropriate standards.
This includes consideration of how to
weigh the uncertainties in the reported
associations between daily or annual
average PM2.5 exposures and mortality
or morbidity in the epidemiologic
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studies. Such an approach is consistent
with setting standards that are neither
more nor less stringent than necessary,
recognizing that a zero-risk standard is
not required by the CAA.
Thus, in recognizing the need to
weigh these uncertainties in reaching
decisions on alternative standard levels
to propose, the Administrator judges
that it is most appropriate to examine
where the evidence of associations
observed in the epidemiologic studies is
strongest and, conversely, where he has
appreciably less confidence in the
associations observed in the
epidemiologic studies. Based on
information evaluated in the 2019 ISA
and ISA Supplement, the Administrator
recognizes that health effects may occur
over the full range of concentrations
observed in the long- and short-term
epidemiologic studies and that no
discernible threshold for any effects can
be identified based on the currently
available evidence (U.S. EPA, 2019a,
section 1.5.3, U.S. EPA, 2022a, section
2.2.3.1 and 2.2.3.2). He also recognizes,
in taking note of CASAC advice and the
distributional statistics analysis
discussed in section II.B.3.b above and
in the PA, that there is significantly
greater confidence in observed
associations over certain parts of the air
quality distributions in the studies, and
conversely, that there is significantly
diminished confidence in ascribing
effects to concentrations toward the
lower part of the distributions.
The Administrator notes that in
previous reviews, evidence-based
approaches noted that the evidence of
an association in any epidemiologic
study is ‘‘strongest at and around the
long-term average where the data in the
study are most concentrated’’ (78 FR
3140, January 15, 2013). Given this,
these approaches focused on identifying
standard levels near or somewhat below
long-term mean concentrations reported
in key epidemiologic studies. These
approaches were supported by previous
CASAC advice. The current CASAC also
supported assessing the mean (or
median) concentrations, but also
suggested additional approaches that
could be explored.100 In utilizing this
evidence-based approach, the
Administrator looks to study-reported
100 The Administrator notes that some members
of the CASAC advised that ‘‘use of the mean to
define where the data provide the most evidence is
conservative. . .’’ (Sheppard, 2022a, p. 3 of
consensus letter) and advised that ‘‘for the purpose
of informing the adequacy of the standards’’
(Sheppard, 2022a, p. 8 of consensus responses) that
the EPA in future reviews include evaluation of
other metrics, including the distribution of
concentrations reported in epidemiologic studies
and in analyses restricting concentrations to below
the current standard level.
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means from the key epidemiologic
studies (as shown in Figure 1 and Figure
2) available in this reconsideration. He
notes that there have been new
approaches to estimating exposure
concentrations since the 2012 review,
such that many of the available key
epidemiologic studies include new
approaches that apply hybrid modeling
techniques to estimate exposures. In
looking at the epidemiologic studies, he
considers these studies in two groups:
(1) monitor-based studies
(epidemiologic studies that used
ground-based monitors to estimate
exposure, similar to approaches used in
past reviews), and (2) hybrid modelingbased studies (epidemiologic studies
that used hybrid modeling approaches
to estimate exposures). As such, he
recognizes that reported mean PM2.5
concentrations in monitor-based studies
are averaged across monitors in each
study area with multiple monitors,
referred to as a composite monitor
concentration, in contrast to the highest
concentration monitored in the study
area, referred to as a maximum monitor
concentration (i.e., the ‘‘design value’’
concentration), which is used to
determine whether an area meets a
given standard. Further, he recognizes
that studies that use hybrid modeling
approaches employ methods to estimate
ambient PM2.5 concentrations across
large geographical areas, including those
without monitors, and thus, when
compared to monitor-based studies,
require additional information to inform
the relationship between the estimated
PM2.5 concentrations across an area to
the maximum monitor design values
used to assess compliance. For the key
U.S. monitor-based epidemiologic
studies, the study reported mean
concentrations range from 9.9–16.5 mg/
m3 and for the U.S. hybrid modeling
based key epidemiologic studies, the
mean concentrations range from 9.3–
12.2 mg/m3.
In thinking further about the
relationship between mean PM2.5
concentrations in key epidemiologic
studies and annual design values, the
Administrator specifically notes that in
a given area, the area design value is
determined by the monitor in an area
with the highest PM2.5 concentrations
and is used to determine compliance
with the standard. He observes, as
detailed above in the air quality
analyses in section I.D.5, that the
highest PM2.5 concentrations spatially
distributed in the area would generally
occur at or near the area design value
monitor and that PM2.5 concentrations
will be equal to or lower at other
monitors in the area. Furthermore, since
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monitoring strategies aim to site
monitors in areas with higher
concentrations, monitored areas will
generally have higher concentrations
than areas without monitors. Thus,
when a study reports a mean that
reflects the average of annual average
measured concentrations for an area, the
area design value will generally be
higher. Similarly, when a study reports
a mean that reflects the average of
annual average concentrations estimated
at various points across an area using a
hybrid modeling approach, the area
design value will generally be higher.
More specifically, the Administrator
observes that the additional air quality
analyses (described in section I.D.5)
suggest that the area annual design
value is greater than the study-reported
mean values by 10–20% for monitorbased studies and 15–18% for hybrid
modeling with population weighting
applied.101 As such, the Administrator
observes that a policy approach for
setting a standard level that requires the
design value monitor to meet studyreported means will generally result in
lower concentrations of PM2.5 across the
entire area, such that even those people
living near an area design value monitor
(where PM2.5 concentrations are
generally highest) will be exposed to
PM2.5 concentrations below the air
quality conditions reported in the
epidemiologic studies where there is the
highest confidence of an association.102
In addition, he specifically notes that an
annual standard level that is no more
than 10–20% higher than the studyreported means in the U.S. monitorbased studies (i.e., for the lowest study
reported mean value of 9.9 mg/m3, this
means an annual standard level of
approximately 10.9–11.9 mg/m3) and no
more than 15–18% higher for the U.S.
hybrid modeling with population
weighting applied (i.e., for the lowest
101 The Administrator also notes that there are a
limited number of studies that report a study mean
that does not reflect the exposure concentrations
used in the epidemiologic study to assess the
reported association. These studies do not report
population-weighted study means and are not
considered here given the substantial difference in
concentrations used to assess the association versus
those used to calculate the study-reported means.
102 Based on the available air quality information,
it would be expected that an area with a study
reported mean of 10 mg/m3 would have a gradient
of concentrations across the area, with higher
concentrations near the design value monitor and
lower concentrations away from it. If the level of
the standard were revised to 10.0 mg/m3, then it
would be expected that there would still be a
gradient of concentrations, but the PM2.5
concentrations across the area would be reduced in
order to meet the revised standard at the design
value monitor, and therefore areas away from the
design value monitor would be expected to have a
gradient of PM2.5 concentrations at or below 10.0
mg/m3 as well.
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study reported mean value of 9.3 mg/m3,
this means an annual standard level of
approximately 10.7–11.0 mg/m3), would
generally maintain air quality exposures
at or below those associated with the
study-reported mean PM2.5
concentrations, exposures for which we
have the strongest support for adverse
health effects occurring. Based on this,
the Administrator concludes that a
revised standard level of 9.0 to 10.0 mg/
m3 would generally limit air quality
exposures to levels well below those
associated with the study-reported mean
PM2.5 concentrations in the key
epidemiologic studies. A revised
standard level of 11.0 mg/m3 would
maintain air quality exposures to below
those associated with most of these
study-reported means, and a revised
standard level of 8.0 mg/m3 would
maintain air quality exposures to far
below all of these study-reported means.
The Administrator notes that every
member of the CASAC found that the
information on study-reported means
supported revising the annual standard
level to 10.0 mg/m3, with the minority of
the CASAC advising that these data also
supported a revised annual standard
level of 10.0–11.0 mg/m3 and the
majority of the CASAC advising that
these study-reported means, in
conjunction with additional bodies of
evidence, supported a revised annual
standard level of 8.0–10.0 mg/m3.
The Administrator also considers
additional information from
epidemiologic studies, consistent with
CASAC advice, to take into account the
broader distribution of PM2.5
concentrations, including the 25th
percentiles of the distributions, and the
degree of confidence in the observed
associations over the broader air quality
distribution. In considering this
additional information, he understands
that the PA presented information on
the distributions of PM2.5
concentrations, when available, from
key epidemiologic studies to provide a
general frame of reference as to the part
of the distribution within which the
data become appreciably more sparse
and, thus, where his confidence in the
associations observed in epidemiologic
studies would become appreciably less.
As discussed in section II.B.3.b above
and presented in Figure 1 and Figure 2
above, he observes that most studies do
not report such data and the
conclusions that can be drawn from
such information across the full body of
evidence are quite limited. However, the
Administrator takes note of additional
population-level data that are available
and in considering the long-term PM2.5
concentrations associated with the 25th
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percentile values of the population-level
data for the studies for which such data
are available, he observes that for the
three key U.S. epidemiologic studies
that use hybrid modeling approaches
that apply population weighting and
report these data, the values reported
were 6.7 mg/m3, 9.1 mg/m3 and 9.1 mg/
m3. For the U.S.-based studies that use
ground-based monitors, the 25th
percentiles ranged from 11.5 mg/m3 to
just below 13.0 mg/m3.
The Administrator notes that there are
substantial uncertainties associated with
using 25th percentile data for purposes
of setting this standard and these
uncertainties are heightened by the
relatively few studies which report such
data and the fact that, by definition, this
data is relatively less common even
within a study for which it is reported.
At the same time, the Administrator is
conscious of his obligation to set
primary standards with an adequate
margin of safety and recognizes that
some members of the CASAC advised
that these data indicate that effects are
occurring below the reported means of
studies. Balancing these concerns about
the need to provide some protection
against uncertain risks with the
obligation to not set standards that are
more stringent than necessary, the
Administrator preliminarily concludes
that a revised standard should limit
exposures to ambient concentrations
near the 25th percentile of reported
studies. Given this consideration, the
Administrator recognizes that a
standard level of 8.0–10.0 mg/m3 is
generally within the range of these
values, while a standard level of 11.0
mg/m3 is above the 25th percentile
values reported in the hybrid modelbased studies but below the 25th
percentile values in studies that use
ground-based monitors. Based on this,
the Administrator recognizes that a
standard within the range of 8.0–11.0
mg/m3 would limit exposures to ambient
concentrations near the 25th percentile
reported in the available studies, with
the lower end of this range further
limiting those exposures.
The Administrator also takes into
consideration the long-term mean PM2.5
concentrations reported in Canadian
epidemiologic studies that, in the
context of the larger body of available
evidence, provided support for causal or
likely to be causal determinations
between PM2.5 exposure and health
effects, as summarized in the 2019 ISA
and ISA Supplement. He notes that the
study-reported means from these
Canadian studies tend to be somewhat
lower than those reported from the key
epidemiologic studies in the U.S.
ranging from 6.9–13.3 mg/m3 for the
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monitor-based studies and 5.9–9.8 mg/
m3 for the hybrid model-based studies.
However, the Administrator is also
mindful that there are important
differences between the exposure
environments in the U.S. and Canada
and that interpreting the data (e.g., mean
concentrations) from the Canadian
studies in the context of a U.S.-based
standard may present challenges in
directly and quantitatively informing
decisions regarding potential alternative
levels of the annual standard, as
detailed above. He additionally notes
that the majority of the CASAC pointed
to the Canadian studies as supporting
their recommendation to revise the
annual standard level to within the
range of 8.0–10.0 mg/m3. Based on this,
the Administrator is not excluding
Canadian studies from his consideration
in this reconsideration, but he is
considering them in light of the
limitations and challenges presented.
The Administrator also notes that the
CASAC recommended looking at the
studies that included analyses that
restrict annual average PM2.5
concentrations to concentrations below
the level of the current annual standard
in evaluating an appropriate range of
levels for a revised annual standard. In
this reconsideration, there are two key
studies available (Di et al., 2017b and
Dominici et al., 2019) that restrict
annual average PM2.5 concentrations to
less than 12 mg/m3. These restricted
analyses report positive and statistically
significant associations with all-cause
mortality, and both report mean PM2.5
concentrations of 9.6 mg/m3. The
Administrator does note that
uncertainties exist in these analyses
(described in more detail in sections
II.B.3.b and II.D.2.a above), including
uncertainty in how the studies exclude
concentrations (e.g., at what spatial
resolution are concentrations being
excluded), which would make it
difficult to compare concentrations in
restricted analyses directly to design
values. However, he does note that an
annual standard level of 9.0–10.0 mg/m3
would be close to these reported mean
values, while a standard level of 11.0
mg/m3 would be above and a standard
level of 8.0 mg/m3 would be much
further below.
The Administrator additionally
considers recent U.S. accountability
studies, which assess the health effects
associated with actions that improve air
quality (e.g., air quality policies or
implementation of an intervention). The
Administrator notes that there are three
studies available in this reconsideration
(Henneman et al. (2019b), Corrigan et al.
(2018), and Sanders et al. (2020a)) that
account for changes in PM2.5
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concentrations due to implementation
of policies and assess whether there was
evidence of changes in associations with
mortality or cardiovascular morbidity
due to changes in annual PM2.5
concentrations. The Administrator notes
that in each of these studies, prior to
implementation of the policies, mean
PM2.5 concentrations were below the
level of the current annual standard
level (12.0 mg/m3) and ranged from 10.0
mg/m3 to 11.1 mg/m3. The Administrator
notes that these studies report positive
and significant associations between
mortality and cardiovascular morbidity
and reductions in ambient PM2.5
(described above in section II.B.3.b and
in Table 3–12 of the PA) and notes that
these studies suggest public health
improvements may occur following the
implementation of a policy that reduces
annual average PM2.5 concentrations
below the level of the current standard
of 12.0 mg/m3. The Administrator notes
that a revised annual standard level of
9.0–10.0 mg/m3 would be at or below the
lowest starting concentration of these
accountability studies (i.e., 10.0 mg/m3).
In addition to the evidence, the
Administrator also considers the results
of the risk assessment. The PA includes
a risk assessment that estimates PM2.5attributable mortality risk associated
with PM2.5 air quality that has been
adjusted to simulate ‘‘just meeting’’ the
current standards, as well as potential
alternative standards. These analyses of
PM2.5-attributable mortality use input
data that include C–R functions from
epidemiologic studies that have nothreshold and a linear C–R relationship
down to zero, as well an air quality
adjustment approach that incorporates
proportional decreases in PM2.5
concentrations to meet lower standard
levels. Such an approach does not
incorporate any elements of uncertainty
in associations of health effects at lower
concentrations and simulated air quality
improvements will always lead to
proportional decreases in risk (i.e., each
additional mg/m3 reduction produces
additional benefits with no clear
stopping point). Therefore, the
Administrator recognizes that the risk
estimates can help to place the evidence
for specific health effects into a broader
public health context, but should be
considered along with the inherent
uncertainties and limitations of such
analyses when informing judgments
about the potential for additional public
health protection associated with PM2.5
exposure and related health effects.
The risk assessment estimates that the
current primary PM2.5 standards could
allow a substantial number of PM2.5associated deaths in the U.S.
Additionally, compared to the current
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annual standard, meeting a revised
annual standard with a lower level is
estimated to reduce PM2.5-associated
health risks in the 30 study areas
controlled by the annual standard by
about 7–9% for a level of 11.0 mg/m3,
15–19% for a level of 10.0 mg/m3, 22–
28% for a level of 9.0 mg/m3, and 30–
37% for a level of 8.0 mg/m3) (U.S. EPA,
2022a, Table 3–17). The CASAC
concurred with the PA’s assessment that
meaningful risk reductions will result
from lowering the annual PM2.5
standard (Sheppard, 2022a, p. 16 of
consensus responses).
The PA also provides information on
the distribution of concentrations
associated with the estimated mortality
risk at each alternative standard level
assessed (U.S. EPA, 2022a, sections
3.4.2.2 and 3.6.2.2, Figure 3–18 and 3–
19). Further evaluating these results can
help clarify the percentage of the
exposure reductions that fall within the
range of concentrations in which there
is the most confidence in the
associations and thus, confidence that
estimated risk reductions will actually
occur. When meeting a standard level of
11.0 mg/m3, the risk is estimated to be
associated with exposure concentrations
that are generally greater than 10.0 mg/
m3, while for a standard level of 10.0
mg/m3, the majority of the days
contributing to the risk estimates are
estimated to be below 10.0 mg/m3. When
meeting an annual standard or 9.0 mg/
m3, the majority of the exposure
concentrations are estimated to be 8.0–
9.0 mg/m3, while for a standard level of
8.0 mg/m3, most of the days are below
8.0 mg/m3. The Administrator notes that
the evidence suggests that majority of
the study-reported means are above 10.0
mg/m3 (concentrations at which the
evidence is the strongest in supporting
an association between exposure to
PM2.5 and adverse health effects
observed in the key epidemiologic
studies available in this reconsideration)
and that at PM2.5 concentrations less
than 8.0 mg/m3, the 2019 ISA notes that
uncertainties remain in the shape of the
C–R curve. He thus recognizes that there
is increasing uncertainty in quantitative
estimates of PM2.5-associated mortality
risk for alternative standard levels at the
lower end of the range of 8.0–11.0 mg/
m3.
As discussed more above, the
Administrator also recognizes that the
risk assessment was able to include an
at-risk analysis that estimated the
potential long-term PM2.5-attributable
exposure and mortality risk in older
adults, stratified by racial/ethnic
demographics, when meeting a revised
annual standard with a lower level.
While the Administrator recognizes that
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this analysis is subject to the multiple
uncertainties and limitations (sections
II.C.2 and II.D.2.b), he does note that the
analysis suggests that a revised annual
standard level within the range of 8.0 to
11.0 mg/m3 is estimated to reduce PM2.5
exposure and may also help to mitigate
risks. Based on the case study areas
included in the analysis, The
Administrator notes that what urban
areas are included in the risk
assessment analysis will greatly
influence the results but notes that
based on the areas included in the
analyses, the results show the largest
impact is on reducing exposure and risk
in Black populations, who were
estimated in the risk assessment case
study areas to have the highest levels of
exposures and the greatest rates of
premature mortality risk. The
Administrator also notes that, similar to
the main risk estimates discussed above,
there is increasing uncertainty in
quantitative estimates of stratified risk
estimates at the lower end of the range
of standard levels assessed.
The Administrator recognizes that
judgments about the appropriate weight
to place on any of the factors discussed
above should reflect consideration not
only of the relative strength of the
evidence but also of the important
uncertainties that remain in the
evidence and the quantitative
information being considered in this
reconsideration. The Administrator also
recognizes that the CAA requires him to
set standards that in his judgment are
neither more stringent nor less stringent
than necessary to protect public health
with an adequate margin of safety.
Based on the above considerations, the
Administrator concludes that it is
appropriate to propose to set a level for
the primary annual PM2.5 standard
within the range of 9.0 to 10.0 mg/m3,
while also taking comment on a level for
the primary annual PM2.5 standard as
low as 8.0 mg/m3 and as high as 11.0 mg/
m3. The Administrator provisionally
concludes that a standard level within
the range of 9.0 to 10.0 mg/m3 would
reflect appropriate approaches to
placing the most weight on the strongest
available evidence, while placing less
weight on much more limited evidence
and on more uncertain analyses of
information available from a relatively
small number of studies. He notes that
a standard set at 9.0 to 10.0 mg/m3
would be at or below the study-reported
mean PM2.5 concentrations in the key
U.S. epidemiologic studies, exposures
for which we have the strongest support
for adverse health effects occurring.
Further, in considering margin of safety,
he notes that an annual standard level
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that is no more than 10–20% higher
than the study-reported means in the
U.S. monitor-based studies (i.e., for the
lowest study reported mean value of 9.9
mg/m3, this means an annual standard
level of approximately 10.9–11.9 mg/m3)
and no more than 15–18% higher for the
U.S. hybrid modeling with population
weighting (i.e., for the lowest study
reported mean value of 9.3 mg/m3, this
means an annual standard level of
approximately 10.7–11.0 mg/m3), would
generally maintain air quality exposures
at or below those associated with the
study-reported mean PM2.5
concentrations. Additionally, the
Administrator also notes that these key
U.S. epidemiologic studies utilize
cohorts that include populations
identified as at-risk, including children
and older adults, as well as individuals
in the general population with preexisting disease, like cardiovascular
disease and respiratory disease. Based
on this information, he concludes that a
revised standard level of 9.0–10.0 mg/m3
would limit air quality exposures to
concentrations well below those
associated with the study reported
mean, studies which include and assess
impacts on the most at-risk populations.
Thus, the Administrator provisionally
concludes that a standard level within
this range would appropriately provide
an adequate margin of safety for the
populations most at risk for adverse
health effects associated with exposure
to PM2.5.
The Administrator also considers
other lines of evidence, including the
study reported means from
epidemiologic studies that restrict
concentrations to levels below 12 mg/m3,
the 25th percentiles values reported by
a subset of epidemiologic studies, and
the information from the accountability
studies. He notes that a standard in the
range of 9.0 to 10.0 mg/m3 would limit
exposures to ambient concentrations
near the 25th percentile reported in the
available studies, with a standard level
of 9.0 mg/m3 limiting those exposures
somewhat more than a standard level of
10.0 mg/m3. He also notes that a
standard in the range of 9.0 to 10.0 mg/
m3 would be near the value of the study
reported means from the two available
long-term restricted analyses studies
(i.e., 9.6 mg/m3). The Administrator
notes a standard level of 9.0–10.0 mg/m3,
would also be at or below the lowest
starting concentration of the newest
available accountability studies (i.e.,
10.0–11.1 mg/m3). The Administrator
also considers the results from the risk
assessment. He recognizes that the risk
estimates should be considered along
with the inherent uncertainties and
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limitations of such analyses when
informing judgments about the potential
for additional public health protection
associated with PM2.5 exposure and
related health effects. When looking at
the risk assessment results, he notes that
an annual standard level of 9.0–10.0 mg/
m3 is estimated to reduce exposure
concentrations such that those
remaining risks are associated with
exposure concentrations that are below
most of the study-reported means in the
key U.S. epidemiologic studies, where
we have the strongest support for
adverse health effects occurring, and
below PM2.5 concentrations (i.e., 8 mg/
m3) where the 2019 ISA notes that
uncertainties remain in the shape of the
C–R curve, particularly for a standard
level as low as 9.0 mg/m3. Lastly, the
Administrator also notes that every
member of the CASAC found that the
available scientific evidence and
information supported revising the
annual standard level to a level of 10.0
mg/m3. Additionally, the majority of the
CASAC also recommended that the
available evidence and information
supported revision to a level of 9.0 mg/
m3. Thus, recognizing the uncertainties
in the evidence and the necessity of
providing requisite protection, with an
adequate margin of safety, the
Administrator is proposing to set the
level of the annual standard in the range
of 9.0–10.0 mg/m3, and solicits
comments on the appropriate standard
level within that range.
While the Administrator recognizes
that some members of the CASAC
advised, and the PA concluded, that the
available scientific information provides
support for considering a range that
extends up to 11.0 mg/m3 and down to
8.0 mg/m3, he provisionally concludes
that proposing such an extended range
would not be appropriate at this time.
More specifically, the Administrator
provisionally concludes that proposing
to revise the annual standard level to
above 10.0 mg/m3 and as high as 11.0 mg/
m3 would reflect a public health policy
approach that would place less weight
on setting a standard level at or below
the study-reported means from a
number of key U.S. epidemiologic
studies and less weight on the risk
assessment results. Such an approach
would also place little or no weight on
the study reported means from
epidemiologic studies that restrict
concentrations to below 12 mg/m3 and
the 25th percentile concentrations
reported by a subset of epidemiologic
studies. The Administrator notes that
such an approach may fail to provide an
adequate margin of safety in light of the
evidence available in this
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reconsideration. In considering revision
to the annual standard level to below
9.0 mg/m3 and as low as 8.0 mg/m3, the
Administrator notes that such a level
would be substantially below the studyreported means and would not
recognize the controlling nature of the
design value monitor with respect to the
concentration gradients consistently
occurring across urban areas. The
Administrator also recognizes that the
evidence and uncertainties for public
health benefits of lower standards exists
on a continuum across the range of
possible standard levels. He
preliminarily judges that the evidence is
sufficient to support standards in the
range of 9.0–10.0 mg/m3, recognizing
that the selection of a final standard
level will depend on judgments about
the relative weight to place on various
aspects of the evidence and how to
provide for an adequate margin of
safety. However, the Administrator
preliminarily judges that the available
information and evidence are not
sufficient to warrant revising the level of
the annual standard below 9.0 mg/m3.
He finds the uncertainties as to the
public health risks and benefits
associated with such a standard to be
too great at this time. Nonetheless,
while the Administrator notes these
considerations above, he solicits
comment on revising the annual
standard down to a level below 9.0 mg/
m3 and as low as 8.0 mg/m3, as well as
to above 10.0 mg/m3 and as high as 11.0
mg/m3, and on approaches for
interpreting the scientific evidence and
rationales that would support such a
level.
E. Proposed Decisions on the Primary
PM2.5 Standards
Taking the above considerations into
account, upon reconsidering the current
primary PM2.5 standards in light of the
currently available scientific evidence
and quantitative information, the
Administrator proposes to revise the
level of the primary annual PM2.5
standard from 12.0 mg/m3 to within the
range of 9.0 to 10.0 mg/m3 and to retain
the 24-hour standard level at 35 mg/m3.
In the Administrator’s judgment, such a
suite of primary PM2.5 standards and the
rationale supporting such levels could
reasonably be judged to reflect the
appropriate consideration of the
strength of the available evidence and
other information and their associated
uncertainties and the advice of the
CASAC.
The Administrator recognizes that the
final suite of standards will reflect the
Administrator’s ultimate judgments in
the final rulemaking as to the suite of
primary PM2.5 standards that are
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requisite to protect the public health
with an adequate margin of safety from
effects associated with PM2.5 exposures.
The final judgments to be made by the
Administrator will appropriately
consider the requirement for standards
that are neither more nor less stringent
than necessary and will recognize that
the CAA does not require that primary
standards be set at a zero-risk level, but
rather at a level that reduces risk
sufficiently so as to protect public
health with an adequate margin of
safety.
Having reached his provisional
judgment to propose revising the annual
standard level from 12.0 to within a
range of 9.0 to 10.0 mg/m3 and to
propose retaining the 24-hour standard
level at 35 mg/m3, the Administrator
solicits public comment on this range of
levels and on approaches to considering
the available evidence and information
that would support the choice of levels
within this range. The Administrator
also solicits public comment on
alternative annual standard levels down
to 8.0 mg/m3 and up to 11.0 mg/m3, on
an alternative 24-hour standard level as
low as 25 mg/m3 and on the combination
of annual and 24-hour standards that
commenters may believe is appropriate,
along with the approaches and
rationales used to support such levels.
For example, the EPA solicits comments
on the uncertainties in the reported
associations between daily or annual
average PM2.5 exposures and mortality
or morbidity in the epidemiologic
studies, the significance of the 25th
percentile of ambient concentrations
reported in studies, the relevance and
limitations of international studies, and
other topics discussed in section
II.D.3.b.
III. Rationale for Proposed Decisions on
the Primary PM10 Standard
This section presents the rationale for
the Administrator’s proposed decision
to retain the existing primary PM10
standard. This decision is based on a
thorough review of the latest scientific
information, published through January
2018,103 and evaluated in the 2019 ISA,
on human health effects associated with
PM10–2.5 in ambient air. As described in
section 1.2 of the ISA Supplement, the
103 In addition to the review’s opening ‘‘call for
information’’ (79 FR 71764, December 3, 2014), the
current ISA identified and evaluated studies and
reports that have undergone scientific peer review
and were published or accepted for publication
between January 1, 2009 through approximately
January 2018 (U.S. EPA, 2019a, p. ES–2). References
that are cited in the 2019 ISA, the references that
were considered for inclusion but not cited, and
electronic links to bibliographic information and
abstracts can be found at: https://hero.epa.gov/hero/
particulate-matter.
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scope of the updated scientific
evaluation of the health effects evidence
is based on those PM size fractions,
exposure durations, and health effects
category combinations where the 2019
ISA concluded a causal relationship
exists (U.S. EPA, 2019a, U.S. EPA,
2022a). Therefore, because the 2019 ISA
did not conclude a causal relationship
for PM10–2.5 for any exposure durations
or health effect categories, the ISA
Supplement does not include an
evaluation of additional studies for
PM10–2.5. As a result, the 2019 ISA
continues to serve as the scientific
foundation for assessing the adequacy of
the primary PM10 standard in this
reconsideration of the 2020 final
decision (U.S. EPA, 2019a, section 1.7;
U.S. EPA, 2022a). The Administrator’s
rationale also takes into account: (1) the
PA evaluation of the policy-relevant
information in the 2019 ISA; (2) CASAC
advice and recommendations, as
reflected in discussions of the draft of
the PA at public meetings and in the
CASAC’s letter dated March 18, 2022, to
the Administrator; and (3) public
comments received during the
development of the PA.
In presenting the rationale for the
Administrator’s proposed decision and
its foundations, section III.A provides
background and introductory
information for this reconsideration of
the primary PM10 standard. It includes
background on the 2020 final decision
to retain the primary PM10 standard
(section III.A.1) and also describes the
general approach for this
reconsideration (section III.A.2) Section
III.B summarizes the key aspects of the
currently available scientific evidence
for PM10–2.5-related health effects.
Section III.C presents the
Administrator’s proposed conclusions
regarding the adequacy of the primary
PM10 standard (section III.C.3), drawing
on evidence-based considerations
(section III.C.2) and advice from the
CASAC (section III.C.1).
A. General Approach
The current primary PM10 standard
was affirmed in 2020 based on the
scientific information available at that
time, as well as the Administrator’s
judgments regarding the available
public health effects evidence, and the
appropriate degree of public health
protection for the existing standards (85
FR 82725, December 18, 2020). With the
2020 decision, the Administrator
retained the existing 24-hour primary
PM10 standard, with its level of 150 mg/
m3 and its one-expected-exceedance
form on average over three years, to
continue to provide public health
protection against short-term exposures
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to PM10–2.5 (85 FR 82725, December 18,
2020). The subsection below focuses on
the key considerations, and the prior
Administrator’s conclusions, for
PM10–2.5-related health effects and the
adequacy of the primary PM10 standard
in the 2020 review.
1. Background on the Current Standard
In the 2019 ISA, the strongest
evidence for PM10–2.5-related health
effects was for cardiovascular effects,
respiratory effects, and premature
mortality following short-term
exposures. For each of these categories
of effects, the 2019 ISA concludes that
the evidence was ‘‘suggestive of, but not
sufficient to infer, a causal
relationship’’. Specifically, the health
effects evidence evaluated in the 2019
ISA included an expanded body of
scientific evidence that has become
available since the completion of the
2009 ISA linking short-term PM10–2.5 to
health outcomes such as premature
death and hospital visits (U.S. EPA,
2009a; U.S. EPA, 2019a). This evidence
base evaluated the causal relationships
between short-term exposure to PM10–2.5
and a broad range of health effects (U.S.
EPA, 2019a, section 1.4.2). These effects
associated with short-term exposure
ranged from hospital admissions and
emergency department visits for
cardiovascular effects (documented in
epidemiologic studies that reported
PM10–2.5 associations with
cardiovascular hospital admissions and
emergency department visits in study
locations with mean 24-hour average
PM10–2.5 concentrations ranging from 7.4
to 13 mg/m3) and respiratory effects
(documented in epidemiologic studies
that reported PM10–2.5 associations with
respiratory hospital admissions and
emergency department visits in study
locations with mean 24-hour average
concentrations ranging from 5.6 to 16.2
mg/m3) to mortality (documented in
epidemiologic studies that reported
PM10–2.5 associations with mortality in
study areas with mean 24-hour average
concentrations ranging from 6.1 to 16.4
mg/m3). In addition to the epidemiologic
studies, the evidence base included a
small number of controlled human
exposure studies and animal
toxicological studies that provided
insight into the biological plausibility of
these effects. Collectively, the
epidemiologic studies, controlled
human exposure, and animal
toxicological studies, with their
inherent uncertainties, contributed to
the causality determinations of
‘‘suggestive of, but not sufficient to
infer, a causal relationship’’ between
short-term exposures to PM10–2.5 and
cardiovascular effects, respiratory
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effects, cancer, and mortality (U.S. EPA,
2019a, section 1.4.2). The 2019 ISA
includes expanded evidence for the
relationships between long-term
exposures and cardiovascular effects,
metabolic effects, nervous system
effects, cancer, and mortality. While the
evidence available in the 2019 ISA
included additional health outcomes,
including those associated with longterm PM10–2.5 exposure, key limitations
in the evidence that were identified in
the 2009 ISA persist in studies
evaluated in the 2019 ISA.
In considering the available body of
evidence, it was noted in the 2020
review there were considerable
uncertainties and limitations associated
with the experimental evidence for
PM2.5 exposures and health effects, and
as such more weight was placed on the
available epidemiologic evidence.
Therefore, the primary focus in the 2020
review was on multi-city and single-city
epidemiologic studies that evaluated
associations between short-term
PM10–2.5 and mortality, cardiovascular
effects (hospital admissions and
emergency department visits, as well as
blood pressure and hypertension), and
respiratory effects. Despite differences
in the approaches 104 used to estimate
ambient PM10–2.5 concentrations, the
majority of the studies reported positive,
though often not statistically significant,
associations with short-term PM10–2.5
exposures. Most PM10–2.5 effect
estimates remained positive in
copollutant models that included either
gaseous pollutants or other particulate
matter size fractions (e.g., PM2.5). In U.S.
study locations likely to have met the
PM10 standard during the study period,
a few studies reported positive
associations between PM10–2.5 and
mortality that were statistically
significant and remained so in
copollutant models (U.S. EPA, 2019a).
In addition to the epidemiologic studies,
there were a small number of controlled
human exposure studies evaluated in
the 2019 ISA that reported alterations in
heart rate variability or increased
pulmonary inflammation following
short-term exposure to PM10–2.5,
providing some support for the
associations in the epidemiologic
studies. Animal toxicological studies
examined the effect of short-term
104 As discussed further below, methods
employed by the epidemiologic studies to estimate
ambient PM10–2.5 concentrations include: (1)
calculating the difference between PM10 and PM2.5
at co-located monitors, (2) calculating the difference
between county-wide averages of monitored PM10
and PM2.5 based on monitors that are not
necessarily co-located, and (3) direct measurement
of PM10–2.5 using a dichotomous sampler (U.S. EPA,
2019a, section 1.4.2).
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PM10–2.5 exposures using non-inhalation
(e.g., intratracheal instillation) route.105
Therefore, these studies provided
limited evidence for the biological
plausibility of PM10–2.5-induced effects
(U.S. EPA, 2019a). Although the
scientific evidence available in the 2019
ISA expanded the understanding of
health effects associated with PM10–2.5
exposures, a number of important
uncertainties remained. These
uncertainties, and their implications for
interpreting the scientific evidence,
include the following:
• The potential for confounding by
copollutants, notably PM2.5, was
addressed with copollutant models in a
relatively small number of PM10–2.5
epidemiologic studies (U.S. EPA,
2019a). This was particularly important
given the relatively small body of
experimental evidence (i.e., controlled
human exposure and animal
toxicological studies) available to
support the independent effect of
PM10–2.5 on human health. This
increases the uncertainty regarding the
extent to which PM10–2.5 itself, rather
than one or more copollutants, is
responsible for the mortality and
morbidity effects reported in
epidemiologic studies.
• There was greater spatial variability
in PM10–2.5 concentrations than PM2.5
concentrations, resulting in the
potential for increased exposure error
for PM10–2.5 (U.S. EPA, 2019a). Available
measurements did not provide sufficient
information to adequately characterize
the spatial distribution of PM10–2.5
concentrations (U.S. EPA, 2019a). The
limitations in estimates of ambient
PM10–2.5 concentrations ‘‘would tend to
increase uncertainty and make it more
difficult to detect effects of PM10–2.5 in
epidemiologic studies’’ (U.S. EPA,
2019a).
• Estimation of PM10–2.5
concentrations over which reported
health outcomes occur remain highly
uncertain. When compared with PM2.5,
there is uncertainty spanning all
epidemiologic studies examining
associations with PM10–2.5 including
deficiencies in the existing monitoring
networks, the lack of a systematic
evaluation of the various methods used
to estimate PM10–2.5 concentrations and
the resulting uncertainty in the spatial
as well as the temporal variability in
PM10–2.5 concentration (U.S. EPA,
2019a). Given these limitations in
routine monitoring, epidemiologic
105 Non-inhalation exposure experiments (i.e.,
intratracheal [IT] instillation) are informative for
size fractions (e.g., PM10–2.5) that cannot penetrate
the airway of a study animal and may provide
information relevant to biological plausibility and
dosimetry (U.S. EPA, 2019a, section A–12).
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studies employed a number of different
approaches for estimating PM10–2.5
concentrations, including (1) calculating
the difference between PM10 and PM2.5
at co-located monitors, (2) calculating
the difference between county-wide
averages of monitored PM10 and PM2.5
based on monitors that are not
necessarily co-located, and (3) direct
measurement of PM10–2.5 using a
dichotomous sampler (U.S. EPA, 2019a,
section 1.4.2). Given the relatively small
number of PM10–2.5 monitoring sites, the
relatively large spatial variability in
ambient PM10–2.5 concentrations, the use
of different approaches to estimating
ambient PM10–2.5 concentrations across
epidemiologic studies, and the
limitations inherent in such estimates,
the distributions of PM10–2.5
concentrations over which reported
health outcomes occur remain highly
uncertain (U.S. EPA, 2019a).
• There was relatively little
information available to characterize the
apparent variability in associations
between short-term PM10–2.5 exposures
and health effects across study locations
(U.S. EPA, 2019a). Specifically, the
relative lack of information on the
chemical and biological composition of
PM10–2.5 as well as potential spatial and
temporal variability in PM10–2.5
exposures complicates the
interpretation of results between study
locations (U.S. EPA, 2009b; U.S. EPA,
2019a).
Consistent with the general approach
routinely employed in NAAQS reviews,
the initial consideration in the 2020
review of the primary PM10 standard
was with regard to the adequacy of
protection provided by the then-existing
standard. Key aspects of that
consideration are summarized below.
i. Considerations Regarding the
Adequacy of the Existing Standard in
the 2020 Review
In the 2020 final decision, the EPA
retained the existing 24-hour primary
PM10 standard with its level of 150 mg/
m3 and its one-expected-exceedance
form on average over three years to
continue to provide public health
protection against exposures to PM10–2.5
(85 FR 82727, December 18, 2020). In
reaching his decision, the Administrator
specifically noted that, while the health
effects evidence was somewhat
expanded since the prior reviews, the
overall conclusions in the 2019 ISA,
including uncertainties and limitations,
were generally consistent with what was
considered in the 2012 review (85 FR
82725, December 18, 2020). In addition,
the Administrator recognized that there
were still a number of uncertainties and
limitations associated with the available
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evidence. With regard to the evidence
on PM10–2.5-related health effects, the
Administrator noted that epidemiologic
studies continued to report positive
associations with mortality and
morbidity in cities across North
America, Europe, and Asia, where
PM10–2.5 sources and composition were
expected to vary widely. While
significant uncertainties remained in the
2020 review, the Administrator
recognized that this expanded body of
evidence had broadened the range of
effects that have been linked with
PM10–2.5 exposures. The studies
evaluated in the 2019 ISA expanded the
scientific foundation presented in the
2009 ISA and led to revised causality
determinations (and new
determinations) for long-term PM10–2.5
exposures and mortality, cardiovascular
effects, metabolic effects, nervous
system effects, and cancer (85 FR 82726,
December 18, 2020). Drawing from his
consideration of this evidence, the
Administrator concluded that the
scientific information available since
the time of the last review supported a
decision to maintain a primary PM10
standard to provide public health
protection against PM10–2.5 exposures,
regardless of location, source of origin,
or particle composition (85 FR 82726,
December 18, 2020). With regard to
uncertainties in the available evidence,
the Administrator first noted that a
number of limitations were identified in
the 2012 review related to: (1) estimates
of ambient PM10–2.5 concentrations used
in epidemiologic studies; (2) limited
evaluation of copollutant models to
address the potential for confounding;
and (3) limited experimental studies
supporting biological plausibility for
PM10–2.5-related effects. Despite the
expanded body of evidence for PM10–2.5
exposures and health effects, the
Administrator recognized that
uncertainties in the 2020 review
continued to include those associated
with the exposure estimates used in
epidemiologic studies, the
independence of the PM10–2.5 health
effect associations, and the biologically
plausible pathways for PM10–2.5 health
effects (85 FR 82726, December 18,
2020). These uncertainties contributed
to the 2019 ISA determinations that the
evidence is at most ‘‘suggestive of, but
not sufficient to infer’’ causal
relationships (85 FR 82726, December
18, 2020). In considering the available
evidence in his basis for the proposed
decision, the Administrator emphasized
evidence supporting ‘‘causal’’ and
‘‘likely to be causal’’ relationships, and
therefore, judged that the PM10–2.5related health effects evidence provided
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an uncertain scientific foundation for
making standard-setting decisions. He
further judged limitations in the
evidence raised questions as to whether
additional public health improvements
would be achieved by revising the
existing PM10 standard (85 FR 24126,
April 30, 2020). In the 2020 decision, for
all of the reasons discussed above and
recognizing the CASAC conclusion that
the evidence provided support for
retaining the current standard, the
Administrator concluded that it was
appropriate to retain the existing
primary PM10 standard, without
revision. His decision was consistent
with the CASAC advice related to the
primary PM10 standard. Specifically, the
CASAC agreed with the 2020 PA
conclusions that, while these effects are
important, the ‘‘evidence does not call
into question the adequacy of the public
health protection afforded by the
current primary PM10 standard’’ and
‘‘supports consideration of retaining the
current standard in this review’’ (Cox,
2019b, p. 3 of consensus letter). Thus,
the Administrator concluded that the
primary PM10 standard (in all of its
elements) was requisite to protect public
health with an adequate margin of safety
against effects that have been associated
with PM10–2.5. In light of this
conclusion, the EPA retained the
existing PM10 standard.
2. General Approach and Key Issues in
This Reconsideration of the 2020 Final
Decision
To evaluate whether it is appropriate
to consider retaining the current
primary PM10 standard, or whether
consideration of revision is appropriate,
the EPA has adopted an approach in
this reconsideration that builds upon
the general approach used in past
reviews and reflects the body of
evidence and information now
available, as well as the assessments and
evaluations performed in those reviews.
As summarized above, the
Administrator’s decision in the 2020
review was based on an integration of
PM10–2.5-related health effects
information with the judgments on the
public health significance of key effects,
policy judgments as to when the
standard is requisite, consideration of
CASAC advice, and consideration of
public comments.
Similarly, in this reconsideration,
information is drawn from recent
studies of PM10–2.5-related health effects.
In so doing, the PA considers
information critically analyzed and
characterized in the 2019 ISA, as well
as consideration of the associated
uncertainties and limitations for the
available evidence.
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B. Overview of the Health Effects
Evidence
The information summarized here is
based on the scientific assessment of the
health effects evidence available in this
reconsideration; this evaluation is
documented in the 2019 ISA and its
policy implications are discussed
further in the PA. As noted above, the
ISA Supplement does not include an
evaluation of studies for PM10–2.5 and
the 2019 ISA continues to serve as the
scientific foundation for this
reconsideration.
1. Nature of Effects
For the health effect categories and
exposure duration combinations
evaluated, the 2019 ISA concludes that
the evidence supports causality
determinations for PM10–2.5 that are at
most ‘‘suggestive of, but not sufficient to
infer, a causal relationship. While the
evidence supporting the causal nature of
relationships between exposure to
PM10–2.5 has been strengthened for some
health effect categories since the
completion of the 2009 ISA, the 2019
ISA concludes that overall ‘‘the
uncertainties in the evidence identified
in the 2009 ISA have, to date, still not
been addressed’’ (U.S. EPA, 2019a,
section 1.4.2, p. 1–41; U.S. EPA, 2022b,
section 4.3.1). Specifically,
epidemiologic studies available in the
2012 review relied on various methods
to estimate PM10–2.5 concentrations, and
these methods had not been
systematically compared to evaluate
spatial and temporal correlations in
PM10–2.5 concentrations. Methods
included: (1) calculating the difference
between PM10 and PM2.5 concentrations
at co-located monitors, (2) calculating
the difference between county-wide
averages of monitored PM10- and PM2.5based on monitors that are not
necessarily co-located, and (3) direct
measurement of PM10–2.5 using a
dichotomous sampler (U.S. EPA, 2019a,
section 1.4.2). As described in the 2019
ISA, there continues to be variability
across epidemiologic studies in the
approaches used to estimate PM10–2.5
concentrations. Additionally, some
studies estimate long-term PM10–2.5
exposures as the difference between
PM10 and PM2.5 concentrations based on
information from spatiotemporal or land
use regression (LUR) models, in
addition to monitors. The various
methods used to estimate PM10–2.5
concentrations have not been
systematically evaluated (U.S. EPA,
2019a, section 3.3.1.1), contributing to
uncertainty regarding the spatial and
temporal correlations in PM10–2.5
concentrations across methods and in
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the PM10–2.5 exposure estimates used in
epidemiologic studies (U.S. EPA, 2019a,
section 2.5.1.2.3). Given the greater
spatial and temporal variability of
PM10–2.5 and the lower number of
PM10–2.5 monitoring sites, compared to
PM2.5, this uncertainty is particularly
important for the coarse size fraction.
Beyond the uncertainty associated with
PM10–2.5 exposure estimates in
epidemiologic studies, the limited
information on the potential for
confounding by copollutants and the
limited support available for the
biological plausibility of health effects
following PM10–2.5 exposures also
continue to contribute to uncertainty in
the PM10–2.5 health evidence.
Uncertainty related to potential
confounding stems from the relatively
small number of epidemiologic studies
that have evaluated PM10–2.5 health
effect associations in copollutants
models with both gaseous pollutants
and other PM size fractions. On the
other hand, uncertainty related to the
biological plausibility of effects
attributed to PM10–2.5 exposures results
from the small number of controlled
human exposure and animal
toxicological studies that have evaluated
the health effects of experimental
PM10–2.5 inhalation exposures. The
evidence supporting the 2019 ISA’s
‘‘suggestive of, but not sufficient to
infer, a causal relationship’’ causality
determinations for PM10–2.5, including
uncertainties in this evidence, is
summarized below in sections III.B.1.a
through III.B.1.f.
a. Mortality
i. Long-Term Exposures
Due to the dearth of studies
examining the association between longterm PM10–2.5 exposure and mortality,
the 2009 ISA concluded that the
evidence was ‘‘inadequate to determine
if a causal relationship exists’’ (U.S.
EPA, 2009a). As reported in the 2019
ISA, some cohort studies conducted in
the U.S. and Europe report positive
associations between long-term PM10–2.5
exposure and total (nonaccidental)
mortality, though results are
inconsistent across studies (U.S. EPA,
2019a, Table 11–11). The examination
of copollutant models in these studies
remains limited and, when included,
PM10–2.5 effect estimates are often
attenuated after adjusting for PM2.5 (U.S.
EPA, 2019a, Table 11–11). Across
studies, PM10–2.5 exposure
concentrations are estimated using a
variety of approaches, including direct
measurements from dichotomous
samplers, calculating the difference
between PM10 and PM2.5 concentrations
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measured at collocated monitors, and
calculating difference of area-wide
concentrations of PM10 and PM2.5. As
discussed above, temporal and spatial
correlations between these approaches
have not been evaluated, contributing to
uncertainty regarding the potential for
exposure measurement error (U.S. EPA,
2019a, section 3.3.1.1 and Table 11–11).
The 2019 ISA concludes that this
uncertainty ‘‘reduces the confidence in
the associations observed across
studies’’ (U.S. EPA, 2019a, p. 11–125).
The 2019 ISA additionally concludes
that the evidence for long-term PM10–2.5
exposures and cardiovascular effects,
respiratory morbidity, and metabolic
disease provide limited biological
plausibility for PM10–2.5-related
mortality (U.S. EPA, 2019a, sections
11.4.1 and 11.4). Taken together, the
2019 ISA concludes that, ‘‘this body of
evidence is suggestive, but not sufficient
to infer, that a causal relationship exists
between long-term PM10–2.5 exposure
and total mortality’’ (U.S. EPA, 2019a, p.
11–125).
ii. Short-Term Exposures
The 2009 ISA concluded that the
evidence is ‘‘suggestive of a causal
relationship between short-term
exposure to PM10–2.5 and mortality’’
(U.S. EPA, 2009a). The 2019 ISA
included multicity epidemiologic
studies conducted primarily in Europe
and Asia that continue to provide
consistent evidence of positive
associations between short-term
PM10–2.5 exposure and total
(nonaccidental) mortality (U.S. EPA,
2019a, Table 11–9). Although these
studies contribute to increasing
confidence in the PM10–2.5-mortality
relationship, the use of a variety of
approaches to estimate PM10–2.5
exposures continues to contribute
uncertainty to the associations observed.
Recent studies expand the assessment of
potential copollutant confounding of the
PM10–2.5-mortality relationship and
provide evidence that PM10–2.5
associations generally remain positive
in copollutant models, though
associations are attenuated in some
instances (U.S. EPA, 2019a, section
11.3.4.1, Figure 11–28, Table 11–10).
The 2019 ISA concludes that, overall,
the assessment of potential copollutant
confounding is limited due to the lack
of information on the correlation
between PM10–2.5 and gaseous pollutants
and the small number of locations in
which copollutant analyses have been
conducted. Associations with causespecific mortality (i.e., cardiovascular
and respiratory mortality) provide some
support for associations with total
(nonaccidental) mortality, though
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associations with respiratory mortality
are more uncertain (i.e., wider
confidence intervals) and less consistent
(U.S. EPA, 2019a, section 11.3.7). The
2019 ISA concludes that the evidence
for PM10–2.5-related cardiovascular
effects provides only limited support for
the biological plausibility of a
relationship between short-term
PM10–2.5 exposure and cardiovascular
mortality (U.S. EPA, 2019a, section
11.3.7). Based on the overall evidence,
the 2019 ISA concludes that, ‘‘this body
of evidence is suggestive, but not
sufficient to infer, that a causal
relationship exists between short-term
PM10–2.5 exposure and total mortality’’
(U.S. EPA, 2019a, p. 11–120).
b. Cardiovascular Effects
i. Long-Term Exposures
In the 2009 ISA, the evidence
describing the relationship between
long-term exposure to PM10–2.5 and
cardiovascular effects was characterized
as ‘‘inadequate to infer the presence or
absence of a causal relationship.’’ The
limited number of epidemiologic
studies reported contradictory results
and experimental evidence
demonstrating an effect of PM10–2.5 on
the cardiovascular system was lacking
(U.S. EPA, 2019a, section 6.4).
The evidence relating long-term
PM10–2.5 exposures to cardiovascular
mortality remains limited, with no
consistent pattern of associations across
studies and, as discussed above,
uncertainty stemming from the use of
various approaches to estimate PM10–2.5
concentrations (U.S. EPA, 2019a, Table
6–70). The evidence for associations
with cardiovascular morbidity has
grown and, while results across studies
are not entirely consistent, some
epidemiologic studies report positive
associations with ischemic heart disease
(IHD) and MI (U.S. EPA, 2019a, Figure
6–34); stroke (U.S. EPA, 2019a, Figure
6–35); atherosclerosis (U.S. EPA, 2019a,
section 6.4.5); venous thromboembolism
(VTE) (U.S. EPA, 2019a, section 6.4.7);
and blood pressure and hypertension
(U.S. EPA, 2019a, Section 6.4.6).
PM10–2.5 cardiovascular mortality effect
estimates are often attenuated, but
remain positive, in copollutants models
that adjust for PM2.5. For morbidity
outcomes, associations are inconsistent
in copollutant models that adjust for
PM2.5, NO2, and chronic noise pollution
(U.S. EPA, 2019a, p. 6–276). The lack of
toxicological evidence for long-term
PM10–2.5 exposures represents a data gap
(U.S. EPA, 2019a, section 6.4.10),
resulting in the 2019 ISA conclusion
that ‘‘evidence from experimental
animal studies is of insufficient quantity
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5633
to establish biological plausibility’’ (U.S.
EPA, 2019a, p. 6–277). Based largely on
the observation of positive associations
in some epidemiologic studies, the 2019
ISA concludes that ‘‘evidence is
suggestive of, but not sufficient to infer,
a causal relationship between long-term
PM10–2.5 exposure and cardiovascular
effects’’ (U.S. EPA, 2019a, p. 6–277).
ii. Short-Term Exposures
The 2009 ISA found that the available
evidence for short-term PM10–2.5
exposure and cardiovascular effects was
‘‘suggestive of a causal relationship.’’
This conclusion was based on several
epidemiologic studies reporting
associations between short-term
PM10–2.5 exposure and cardiovascular
effects, including IHD hospitalizations,
supraventricular ectopy, and changes in
heart rate variability (HRV). In addition,
dust storm events resulting in high
concentrations of crustal material were
linked to increases in total
cardiovascular disease emergency
department visits and hospital
admissions. However, the 2009 ISA
noted the potential for exposure
measurement error primarily due to the
different methods used across studies to
estimate PM10–2.5 concentrations and
copollutant confounding in these
epidemiologic studies. In addition, there
was only limited evidence of
cardiovascular effects from a small
number of experimental studies (e.g.
animal toxicological studies and
controlled human exposure studies) that
examined short-term PM10–2.5 exposures
(U.S. EPA, 2009a, section 6.2.12.2). In
the 2019 ISA, key uncertainties
included the potential for exposure
measurement error, copollutant
confounding, and limited evidence of
biological plausibility for cardiovascular
effects following inhalation exposure
(U.S. EPA, 2019a, section 6.3.13).
The evidence for short-term PM10–2.5
exposure and cardiovascular outcomes
has expanded since the 2009 ISA,
though important uncertainties remain.
The 2019 ISA notes that there are a
small number of epidemiologic studies
reporting positive associations between
short-term exposure to PM10–2.5 and
cardiovascular-related morbidity
outcomes. However, the 2019 ISA notes
that there is limited evidence to support
that these associations are biologically
plausible, or independent of copollutant
confounding. The 2019 ISA also
concludes that it remains unclear how
the approaches used to estimate PM10–2.5
concentrations in epidemiologic studies
compare amongst one another and
subsequently how exposure
measurement error varies between each
method. Specifically, it is unclear how
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well-correlated PM10–2.5 concentrations
are both temporally and spatially across
these methods and therefore whether
exposure measurement error varies
across these methods. Taken together,
the 2019 ISA concludes that ‘‘the
evidence is suggestive of, but not
sufficient to infer, a causal relationship
between short-term PM10–2.5 exposures
and cardiovascular effects’’ (U.S. EPA,
2019a, p. 6–254).
c. Respiratory Effects—Short-Term
Exposures
Based on a small number of
epidemiologic studies observing
associations with some respiratory
effects and limited evidence from
experimental studies to support
biological plausibility, the 2009 ISA
(U.S. EPA, 2009a) concluded that the
relationship between short-term
exposure to PM10–2.5 and respiratory
effects is ‘‘suggestive of a causal
relationship.’’ Epidemiologic findings
were consistent for respiratory infection
and combined respiratory-related
diseases, but not for COPD. Studies
were characterized by overall
uncertainty in the exposure assignment
approach and limited information
regarding potential copollutant
confounding. Controlled human
exposure studies of short-term PM10–2.5
exposures found no lung function
decrements and inconsistent evidence
for pulmonary inflammation. Animal
toxicological studies were limited to
those using non-inhalation (e.g., intratracheal instillation) routes of PM10–2.5
exposure.
Recent epidemiologic findings
consistently link PM10–2.5 exposure to
asthma exacerbation and respiratory
mortality, with some evidence that
associations remain positive (though
attenuated in some studies of mortality)
in copollutant models that include
PM2.5 or gaseous pollutants.
Epidemiologic studies provide limited
evidence for positive associations with
other respiratory outcomes, including
COPD exacerbation, respiratory
infection, and combined respiratoryrelated diseases (U.S. EPA, 2019a, Table
5–36). As noted above for other
endpoints, an uncertainty in these
epidemiologic studies is the lack of a
systematic evaluation of the various
methods used to estimate PM10–2.5
concentrations and the resulting
uncertainty in the spatial and temporal
variability in PM10–2.5 concentrations
compared to PM2.5 (U.S. EPA, 2019a,
sections 2.5.1.2.3 and 3.3.1.1).
Specifically, the existing monitoring
networks do not provide a great sense of
how well correlated concentrations are
both spatially and temporally across the
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PM10–2.5 estimation methods and overall
spatial and temporal patterns in PM10–2.5
concentrations. Taken together, the 2019
ISA concludes that ‘‘the collective
evidence is suggestive of, but not
sufficient to infer, a causal relationship
between short-term PM10–2.5 exposure
and respiratory effects’’ (U.S. EPA,
2019a, p. 5–270).
d. Cancer—Long-Term Exposures
In the 2012 review, little information
was available from studies of cancer
following inhalation exposures to
PM10–2.5. Thus, the 2009 ISA determined
the evidence was ‘‘inadequate to
evaluate the relationship between longterm PM10–2.5 exposures and cancer’’
(U.S. EPA, 2009a). The scientific
information evaluated in the 2019 ISA
of long-term PM10–2.5 exposure and
cancer remains limited, with a few
recent epidemiologic studies reporting
positive, but imprecise, associations
with lung cancer incidence (U.S. EPA,
2019a). Moreover, uncertainty remains
in these studies with respect to
exposure measurement error due to the
use of PM10–2.5 predictions that have not
been validated by monitored PM10–2.5
concentrations (U.S. EPA, 2019a,
sections 3.3.2.3 and 10.3.4). Relatively
few experimental studies of PM10–2.5
have been conducted, though available
studies indicate that PM10–2.5 exhibits
two key characteristics of carcinogens:
genotoxicity and oxidative stress. While
limited, such experimental studies
provide some evidence of biological
plausibility for the findings in a small
number of epidemiologic studies (U.S.
EPA, 2019a, section 10.3.4).
Taken together, the small number of
epidemiologic and experimental
studies, along with uncertainty with
respect to exposure measurement error,
contribute to the determination in the
2019 ISA that, ‘‘the evidence is
suggestive of, but not sufficient to infer,
a causal relationship between long-term
PM10–2.5 exposure and cancer’’ (U.S.
EPA, 2019a, p. 10–87).
e. Metabolic Effects—Long-Term
Exposures
The 2009 ISA did not make a
causality determination for PM10–2.5related metabolic effects. One
epidemiologic study in the 2019 ISA
reports an association between longterm PM10–2.5 exposure and incident
diabetes, while additional crosssectional studies report associations
with effects on glucose or insulin
homeostasis (U.S. EPA, 2019a, section
7.4). As discussed above for other
outcomes, uncertainties with the
epidemiologic evidence include the
potential for copollutant confounding
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and exposure measurement error due to
the different methods used across
studies to estimate PM10–2.5
concentrations (U.S. EPA, 2019a, Tables
7–14 and 7–15). The evidence base to
support the biological plausibility of
metabolic effects following PM10–2.5
exposures is limited, but a crosssectional study that investigated
biomarkers of insulin resistance and
systemic and peripheral inflammation
may support a pathway leading to type
2 diabetes (U.S. EPA, 2019a, sections
7.4.1 and 7.4.3). Based on the expanded,
though still limited evidence base, the
2019 ISA concludes that, ‘‘[o]verall, the
evidence is suggestive of, but not
sufficient to infer, a causal relationship
between [long]-term PM10–2.5 exposure
and metabolic effects’’ (U.S. EPA, 2019a,
p. 7–56).
f. Nervous System Effects—Long-Term
Exposures
The 2009 ISA did not make a
causality determination for PM10–2.5related nervous system effects. In the
2019 ISA, available epidemiologic
studies report associations between
PM10–2.5 and impaired cognition and
anxiety in adults in longitudinal
analyses (U.S. EPA, 2019a, Table 8–25,
section 8.4.5). Associations of long-term
exposure with neurodevelopmental
effects are not consistently reported in
children (U.S. EPA, 2019a, sections
8.4.4 and 8.4.5). Uncertainties in these
studies include the potential for
copollutant confounding, as no studies
examined copollutants models (U.S.
EPA, 2019a, section 8.4.5), and for
exposure measurement error, given the
use of various methods to estimate
PM10–2.5 concentrations (U.S. EPA,
2019a, Table 8–25). In addition, there is
limited animal toxicological evidence
supporting the biological plausibility of
nervous system effects (U.S. EPA,
2019a, sections 8.4.1 and 8.4.5). Overall,
the 2019 ISA concludes that, ‘‘the
evidence is suggestive of, but not
sufficient to infer, a causal relationship’’
between long-term PM10–2.5 exposure
and nervous system effects (U.S. EPA,
2019a, p. 8–75).
C. Proposed Conclusions on the Primary
PM10 Standard
In reaching proposed conclusions on
the current primary PM10 standard
(presented in section III.C.3), the
Administrator has taken into account
policy-relevant evidence-based
considerations discussed in the PA
(summarized in section III.C.2), as well
as advice from the CASAC and public
comments on the standard received thus
far in the reconsideration (section
III.C.1). In general, the role of the PA is
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to help ‘‘bridge the gap’’ between the
Agency’s assessment of the available
evidence, and the judgments required of
the Administrator in determining
whether it is appropriate to retain or
revise the NAAQS. Evidence-based
considerations draw upon the EPA’s
integrated evaluation of the scientific
evidence of PM10–2.5-related health
effects presented in the 2019 ISA
(summarized in section III.B above) to
address key policy-relevant questions in
the reconsideration.
The approach to reviewing the
primary PM10 standard is consistent
with requirements of the provisions of
the CAA related to the review of the
NAAQS and how the EPA and the
courts have historically interpreted the
CAA. As discussed in section I.A above,
these provisions require the
Administrator to establish primary
standards that, in the Administrator’s
judgment, are requisite (i.e., neither
more nor less stringent than necessary)
to protect public health with an
adequate margin of safety. Consistent
with the Agency’s approach across all
NAAQS reviews, the EPA’s approach to
informing these judgments is based on
a recognition that the available health
effects evidence generally reflects a
continuum that includes ambient air
concentrations for which scientists
generally agree that health effects are
likely to occur, through lower
concentrations at which the likelihood
and magnitude of response becomes
increasingly uncertain. The CAA does
not require the Administrator to
establish a primary standard at a zerorisk level or at background
concentration levels, but rather at a
level that reduces risk sufficiently so as
to protect public health, including the
health of sensitive groups, with an
adequate margin of safety.
The proposed decision on the
adequacy of the primary PM10 standard
described below is a public health
policy judgment by the Administrator
that draws on the scientific evidence for
health effects and judgments about how
to consider the uncertainties and
limitations that are inherent in the
scientific evidence. The four basic
elements of the NAAQS (i.e., indicator,
averaging time, form, and level) have
been considered collectively in
evaluating the health protection
afforded by the current standard. The
Administrator’s final decision will
additionally consider public comments
received on this proposed decision.
1. CASAC Advice in This
Reconsideration
The CASAC has provided advice on
the adequacy of the current primary
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PM10 standard in the context of its
review of the draft PA (Sheppard,
2022a).106 In this context, the CASAC
supported the preliminary conclusion in
the draft PA that the evidence reviewed
in the 2019 ISA does not call into
question the public health protection
provided by the current primary PM10
standard against PM10–2.5 exposures and
concurs with the draft PA’s overall
preliminary conclusion that it is
appropriate to consider retaining the
current primary PM10 standard
(Sheppard, 2022a, p. 4 of consensus
letter). Additionally, the CASAC
concurred that ‘‘. . . at this time, PM10
is an appropriate choice as the indicator
for PM10–2.5’’ and ‘‘that it is important to
retain the level of protection afforded by
the current PM10 standard’’ (Sheppard,
2022a, p. 4 of consensus letter). The
CASAC also recognized uncertainties
associated with the scientific evidence,
including ‘‘compared to PM2.5 studies,
the more limited number of
epidemiology studies with positive
statistically significant findings, and the
difficulty in extracting the sole
contribution of coarse PM to observed
adverse health effects’’ (Sheppard,
2022a, p. 19 of consensus responses).
The CASAC recommended several
areas for additional research to reduce
uncertainties in the PM10–2.5 exposure
estimates used in the epidemiologic
studies, to evaluate the independence of
PM10–2.5 health effect associations, to
evaluate the biological plausibility of
PM10–2.5-related effects, and to increase
the number of studies examining
PM10–2.5-related health effects in at-risk
populations (Sheppard, 2022a, p. 20 of
consensus responses). Furthermore, the
CASAC ‘‘recognizes a need for, and
supports investment in research and
deployment of measurement systems to
better characterize PM10–2.5’’ and to
‘‘provide information that can improve
public health’’ (Sheppard, 2022a, p. 20
of consensus responses).
2. Evidence-Based Considerations in the
Policy Assessment
With regard to the current evidence
on health effects associated with long
and short—term PM10–2.5 exposure
health effects, the PA notes that recent
106 A limited number of public comments have
also been received in this reconsideration to date,
including comments focused on the draft PA. Of the
public comments that addressed the adequacy of
the current primary PM10 standard, most
commenters supported the preliminary conclusion
that it is appropriate to consider retaining the
current primary PM10 standard, without revision.
However, one nonprofit organization suggested that
the primary PM10 standard should be strengthened
to a level of 45 mg/m3, consistent with the World
Health Organization Global Air Quality Guideline
(WHO, 2021).
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epidemiologic studies that continue to
report positive associations with
mortality and morbidity in cities across
North America, Europe, and Asia, where
PM10–2.5 sources and composition are
expected to vary widely (U.S. EPA,
2022b, section 4.3.1). While significant
uncertainties remain, as described
below and summarized in the PA (U.S.
EPA, 2022b, section 4.5), the PA
recognizes that this expanded body of
evidence has broadened the range of
effects that have been linked with
PM10–2.5 exposures. The uncertainties in
the available epidemiologic studies
contribute to the determinations in the
2019 ISA that the evidence for shortand long-term exposures to PM10–2.5 and
cardiovascular effects, cancer, and
mortality and long-term PM10–2.5
exposures and metabolic effects and
nervous system effects is ‘‘suggestive of,
but not sufficient to infer’’ causal
relationships (U.S. EPA, 2019a; U.S.
EPA, 2022b, section 4.3.1). Drawing
from this information, the PA concludes
that the evidence continues to provide
support for maintaining a standard that
provides some measure of protection
against exposures to PM10–2.5, regardless
of location, sources of origin, or particle
composition (U.S. EPA, 2022b, section
4.5).
With regard to uncertainties, the PA
recognizes that the 2019 ISA notes that
important uncertainties remain in the
evidence base for PM10–2.5-related health
effects. As summarized in section III.B
above and in the PA (U.S. EPA, 2022b,
sections 4.3.1 and 4.5). These
uncertainties include those related to
variability in PM10–2.5 exposure
estimates used in epidemiologic studies,
in the independence of PM10–2.5 health
effect associations, and in the biological
plausibility of the PM10–2.5-related
health effects. These uncertainties
contribute to the determinations in the
2019 ISA that the evidence for shortand long-term PM10–2.5 exposure in key
health effect categories is ‘‘suggestive of,
but not sufficient to infer’’ causal
relationships (U.S. EPA, 2019a). Taking
this information into consideration, the
PA concludes that, as in previous
reviews, such uncertainties raised
questions regarding the degree to which
additional public health protection
would be achieved by revising the
existing PM10 standard (U.S. EPA,
2022b, section 4.5).
With regard to the indicator for the
primary PM10 standard, the PA notes
that the evidence continues to support
retaining the PM10 indicator to provide
public health protection against
PM10–2.5-related effects. Consistent with
the approaches in previous reviews, a
standard with a PM10 mass-based
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indicator, in conjunction with a PM2.5
mass-based standard, will result in
controlling allowable concentrations of
PM10–2.5. Given that the use of the PM10
indicator does include consideration of
both PM2.5 and PM10–2.5 concentrations,
the 2019 ISA provides a comparison of
the relative contribution of PM2.5 and
PM10–2.5 to PM10 concentrations, finding
that the relative contribution of PM2.5
and PM10–2.5 to PM10 concentrations can
vary across the U.S. by region and
season, with urban locations having a
somewhat higher contribution of PM2.5
contributing to PM10 concentrations
than PM10–2.5 (U.S. EPA, 2019a, section
2.5.1.1.4, Table 2–7). In these urban
locations, where PM2.5 concentrations
are somewhat higher than in rural
locations, the toxicity of the PM10 may
be higher due to contaminating PM2.5.
Further, although uncertainties with the
evidence persist, the strongest health
effects evidence associated with PM10–2.5
comes from epidemiologic studies
conducted in urban areas. In light of this
and consistent with the approaches in
previous reviews, the PA concludes that
a PM10 standard, set at a single
unvarying level, will generally result in
lower allowable concentrations of
PM10–2.5 in urban areas than in
nonurban areas. In this way, the PM10
indicator will target protection by
allowing less PM10–2.5 in areas that
experience high concentrations of
potentially contaminating PM2.5. Thus,
the evidence continues to support
retaining the PM10 indicator.
When the above information is taken
together, the PA concludes that
available evidence does not call into
question the adequacy of the public
health protection provided by the
current primary PM10 standard in order
to protect against PM10–2.5 exposures.
Specifically, the PA notes that while the
evidence supports maintaining a PM10
standard to provide some measure of
protection against PM10–2.5 exposures,
uncertainties in the evidence lead to
questions regarding the potential public
health implications of revising the
existing PM10 standard. Thus, the PA
concludes that the evidence does not
call into question the adequacy of the
public health protection afforded by the
current primary PM10 standard (U.S.
EPA, 2022b, section 4.5).
3. Administrator’s Proposed Decision on
the Current Primary PM10 Standard
This section summarizes the
Administrator’s considerations and
proposed conclusions related to the
current primary PM10 standard and
presents his proposed decision to retain
that standard, without revision. In
establishing primary standards under
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the Act that are ‘‘requisite’’ to protect
the public health with an adequate
margin of safety, the Administrator is
seeking to establish standards that are
neither more nor less stringent than
necessary for this purpose. He
recognizes that the Act does not require
that primary standards be set at a zerorisk level; rather, the NAAQS must be
sufficiently protective, but not more
stringent than necessary.
Given these requirements, and
consistent with the primary PM2.5
standards discussed above (section
II.C.3), the Administrator’s final
decision in this reconsideration of the
current primary PM10 standard will be
a public health policy judgment that
draws upon the scientific information
examining the health effects of PM10–2.5
exposures, including how to consider
the range and magnitude of
uncertainties inherent in that
information. The Administrator
recognizes that his final decision will be
based on an interpretation of the
scientific evidence that neither
overstates nor understates its strengths
and limitations, nor the appropriate
inferences to be drawn.
Consistent with previous reviews, the
Administrator first considers the
available scientific evidence for
PM10–2.5-related exposures and health
effects, as evaluated in the 2019 ISA. As
an initial matter, the Administrator
recognizes that the scientific evidence
for PM10–2.5-related effects available in
this reconsideration is the same body of
evidence that was available at the time
of the 2020 review, as evaluated in the
2019 ISA and summarized in section
III.B above. The 2019 ISA concludes
that the evidence supports ‘‘suggestive
of, but not sufficient to infer’’ causal
relationships between short- and longterm exposures to PM10–2.5 and
cardiovascular effects, cancer, and
mortality and long-term PM10–2.5
exposures and metabolic effects and
nervous system effects (U.S. EPA,
2019a). The Administrator notes that the
evidence for several PM10–2.5-related
health effects has expanded since the
completion of the 2009 ISA, but
important uncertainties remain.
Epidemiologic studies evaluated in the
2019 ISA continue to report positive
associations between short-term
exposure to PM10–2.5 and mortality and
morbidity in cities across North
America, Europe, and Asia, where
PM10–2.5 sources and composition are
expected to vary widely, but across
studies inconsistency remains in the
approaches used to estimate PM10–2.5
exposures. While the Administrator
recognizes that important uncertainties
remain, he also recognizes that the
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expansion in the number of studies
evaluating PM10–2.5 exposures and
health effects since the completion of
the 2009 ISA has broadened the range
of effects that may be linked with
PM10–2.5 exposures. The uncertainties in
the epidemiologic studies contribute to
the determinations in the 2019 ISA that
the evidence for short and long-term
PM10–2.5 exposures and mortality,
cardiovascular effects, metabolic effects,
nervous system effects, and cancer is
‘‘suggestive of, but not sufficient to
infer’’ causal relationships (U.S. EPA,
2019a; U.S. EPA, 2022b, section 4.3.1).
Although most of these studies
examined PM10–2.5 health effect
associations in urban areas, some
studies have also linked mortality and
morbidity with relatively high ambient
concentrations of particles of non-urban
crustal origin from dust storm events
(U.S. EPA, 2019a).
In considering the available evidence,
the Administrator recognizes that the
evidence continues to provide support
for maintaining a standard that provides
some measure of protection against
exposures to PM10–2.5, regardless of
location, source of origin, or particle
composition, consistent with previous
reviews (78 FR 3176, January 15, 2013;
85 FR 82726, December 18, 2020).
Drawing from the evidence evaluated in
the 2019 ISA and consideration of the
scientific evidence in the PA, the
Administrator notes that, consistent
with previous reviews, the 2019 ISA
and the PA highlight a number of
uncertainties associated with the
evidence, including those related to
PM10–2.5 exposure estimates used in
epidemiologic studies, in the
independence of PM10–2.5 health effect
associations, and in the biological
plausibility of the PM10–2.5-related
effects. These uncertainties contribute to
the determinations in the 2019 ISA that
the evidence for short-term PM10–2.5
exposures and key health effects is
‘‘suggestive of, but not sufficient to
infer’’ causal relationships. In
considering the available scientific
evidence, consistent with approaches
employed in past NAAQS reviews, the
Administrator places the most weight
on evidence supporting ‘‘causal’’ and
‘‘likely to be causal’’ relationships. In so
doing, he notes that the available
evidence for short-term PM10–2.5
exposures and health effects does not
support causality determinations of a
‘‘causal relationship’’ or ‘‘likely to be
causal relationship.’’ Furthermore, the
Administrator recognizes that, because
of the uncertainties and limitations in
the evidence base, the PA does not
include a quantitative assessment of
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PM10–2.5 exposures and risk that might
further inform decisions regarding the
adequacy of the current 24-hour primary
PM10 standard. Therefore, in light of the
2019 ISA conclusions that the evidence
supports ‘‘suggestive of, but not
sufficient to infer’’ causal relationships,
specifically for cardiovascular effects,
respiratory effects, cancer, and mortality
and short-term exposures to PM10–2.5,
and the lack of available quantitative
assessments, the Administrator judges
that there are substantial uncertainties
that raise questions regarding the degree
to which additional public health
improvements would be achieved by
revising the existing PM10 standard.
Furthermore, the Administrator
recognizes that the 2019 ISA also
concludes that the evidence supports
‘‘suggestive of, but not sufficient to
infer’’ causal relationships for long-term
PM10–2.5-exposures and cardiovascular
effects, metabolic effects, nervous
system effects, cancer, and mortality.
However, in considering the available
evidence for long-term PM10–2.5
exposures, he notes that there is limited
evidence that would support
consideration of an annual standard to
provide protection against such effects,
in conjunction with the current primary
24-hour PM10 standard. He
preliminarily concludes that the current
primary 24-hour PM2.5 standard that
reduces 24-hour exposures also likely
reduces long-term average exposures,
and therefore provides some margin of
safety against the health effects
associated with long-term PM10–2.5
exposures.
In reaching proposed conclusions on
adequacy of the current primary 24-hour
PM10 standard, the Administrator also
considers advice from the CASAC. As
noted above, the CASAC recognizes
uncertainties associated with the
scientific evidence, including
‘‘compared to PM2.5 studies, the more
limited number of epidemiology studies
with positive statistically significant
findings, and the difficulty in extracting
the sole contribution of coarse PM to
observed adverse health effects’’
(Sheppard, 2022a, p. 19 of consensus
responses). Given these uncertainties,
the CASAC agrees with the PA
conclusion that the scientific evidence
does not call into question the adequacy
of the primary PM10 standard and
supports consideration of retaining the
current standard, noting that ‘‘[t]he
CASAC supports this decision’’
(Sheppard, 2022a, p. 4 of consensus
letter). Additionally, the CASAC
concurred that ‘‘. . . at this time, PM10
is an appropriate choice as the indicator
for PM10–2.5’’ and ‘‘that it is important to
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retain the level of protection afford by
the current PM10 standard’’ (Sheppard,
2022a, p. 4 of consensus letter).
When the above information is taken
together, the Administrator proposes to
conclude that the available scientific
evidence continues to support a PM10
standard to provide some measure of
protection against PM10–2.5 exposures.
This proposed conclusion reflects the
available evidence for PM10–2.5-related
health effects, for both short and longterm exposure, as evaluated in the 2019
ISA. However, he also recognizes that
important limitations in the evidence
remain. Consistent with the decisions in
previous reviews, the Administrator
proposes to conclude that these
limitations lead to considerable
uncertainty regarding the potential
public health implications of revising
the level of the current primary 24-hour
PM10 standard. Thus, based on his
consideration of the evidence and
associated uncertainties and limitations
for PM10–2.5-related health effects, as
described above, and his consideration
of CASAC advice on the primary PM10
standard, the Administrator proposes to
retain the current standard, without
revision. The Administrator solicits
comments on this proposed decision.
Having reached the proposed decision
described here based on the
interpretation of the PM10–2.5-related
health effects evidence, as evaluated in
the 2019 ISA; the evaluation of policyrelevant aspects of the evidence in the
PA; the advice and recommendations
from the CASAC; public comments
received to date in their reconsideration;
and the public health policy judgments
described above, the Administrator
recognizes that other interpretations,
assessments and judgments might be
possible. Therefore, the Administrator
solicits comment on the array of issues
associated with reconsideration of the
primary 24-hour PM10 standard,
including public health and science
policy judgments inherent in his
proposed decision, as described above,
and the rationales upon which such
views are based.
IV. Communication of Public Health
A. Air Quality Index Overview
Information on the public health
implications of ambient concentrations
of criteria pollutants is made available
primarily by Air Quality Index (AQI)
reporting through the EPA’s AirNow
website.107 The current AQI has been in
use since its inception in 1999.108 It
107 See
https://www.airnow.gov/.
1976, the EPA established a nationally
uniform air quality index, then called the Pollutant
Standard Index (PSI), for use by State and local
108 In
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provides useful, timely, and easily
understandable information about the
daily degree of pollution. The goal of
the AQI is to establish a nationally
uniform system of indexing pollution
concentrations for ozone, carbon
monoxide, nitrogen dioxide, PM, and
sulfur dioxide. The AQI is recognized
internationally as a proven tool to
effectively communicate air quality
information to the public. In fact, many
countries have created similar indices
based on the AQI.
The AQI converts an individual
pollutant concentration in a
community’s air to a number on a scale
from 0 to 500. Reported AQI values for
specific pollutants enable the public to
know whether air pollution levels in a
particular location are characterized as
good (0–50), moderate (51–100),
unhealthy for sensitive groups (101–
150), unhealthy (151–200), very
unhealthy (201–300), or hazardous
(301+). Across criteria pollutants, the
AQI index value of 100 typically
corresponds to the level of the shortterm (e.g., 24-hour, 8-hour, or 1-hour
standard) NAAQS for each pollutant.
Below an index value of 100, an
intermediate value of 50 is defined
either as the level of the annual
standard if an annual standard has been
established (e.g., PM2.5, nitrogen
dioxide), a concentration equal to onehalf the value of the 24-hour standard
used to define an index value of 100
(e.g., carbon monoxide), or a
concentration based directly on health
effects evidence (e.g., ozone). An AQI
value greater than 100 means that a
pollutant is in one of the unhealthy
categories (i.e., unhealthy for sensitive
groups, unhealthy, very unhealthy, or
hazardous). An AQI value at or below
100 means that a pollutant
concentration is in one of the
satisfactory categories (i.e., moderate or
good). The scientific evidence on
pollutant-related health effects for each
NAAQS review evaluated in the ISA109
support decisions related to pollutant
concentrations at which to set the
various AQI breakpoints, which
delineate the AQI categories for each
individual pollutant (i.e., the pollutant
concentrations corresponding to index
values of 150, 200, 300, and 500). The
AQI is reported three ways, all of which
agencies on a voluntary basis (41 FR 37660,
September 7, 1976; 52 FR 24634, July 1, 1987). In
August 1999, the EPA adopted revisions to this air
quality index (64 FR 42530, August 4, 1999) and
renamed the index the AQI.
109 In some NAAQS reviews, there may also be an
ISA Supplement or a Provisional Assessment of
scientific evidence that becomes available during a
review after an ISA is finalized. To the extent that
such evidence can inform decisions on the AQI,
that information is also considered.
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are useful and complementary. The
daily AQI is reported for the previous
day and used to observe trends in
community air quality, the AQI forecast
helps people plan their outdoor
activities for the next day, and the nearreal-time AQI, or NowCast AQI, tells
people whether it is a good time for
outdoor activity.
Historically, State and local agencies
have primarily used the AQI to provide
general information to the public about
air quality and its relationship to public
health. For more than two decades,
many states and local agencies, as well
as the EPA and other Federal agencies,
have been developing new and
innovative programs and initiatives to
provide more information related to air
quality and health messaging to the
public in a more timely way. These
initiatives, including air quality
forecasting, near real-time data reporting
through the AirNow website, use of data
from air quality sensors on the Fire and
Smoke Map, and air quality action day
programs, provide useful, up-to-date,
and timely information to the public
about air pollution and its health effects.
Such information can help the public
learn when their well-being may be
compromised, so they can take actions
to avoid or to reduce exposures to
ambient pollution at concentrations of
concern. This information can also
encourage the public to take actions that
will reduce air pollution on days when
concentrations are projected to be of
concern to local communities (e.g., air
quality action day programs can
encourage individuals to drive less or
carpool). The EPA and state, local and
Tribal agencies recognize that these
programs are interrelated with AQI
reporting and with the information
related to the effects of air pollution on
public health that is evaluated through
the periodic review, and revision when
appropriate, of the NAAQS.
B. Air Quality Index Category
Breakpoints for PM2.5
One purpose of the AQI is to
communicate to the public when air
quality is poor and thus when they
should consider taking actions to reduce
their exposures. The higher the AQI
value, the higher the level of air
pollution and the greater the health
concern. In recognition of the scientific
information available that is informing
the reconsideration of the 2020 final
decision on the primary PM2.5
standards, including a number of new
controlled human exposure and
epidemiologic studies published since
the completion of the 2009 ISA, as well
as additional epidemiologic studies
from other peer reviewed documents
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that evaluate the health effects of
wildfire smoke exposure and that can
inform the AQI at higher PM2.5
concentrations, the EPA proposes to
make two sets of changes to the PM2.5
sub-index of the AQI. First, the EPA
proposes to continue to use the
approach used in the revisions to the
AQI in 2012 (77 FR 38890, June 29,
2012) of setting the lower breakpoints
(50, 100 and 150) to be consistent with
the levels of the primary PM2.5 annual
and 24-hour standards and proposes to
revise the lower breakpoints to be
consistent with any changes to the
primary PM2.5 standards that are part of
this reconsideration. Second, the EPA
proposes to revise the upper AQI
breakpoints (200 and above) and to
replace the linear-relationship approach
used in 1999 to set these breakpoints,
with an approach that more fully
considers the PM2.5 health effects
evidence from controlled human
exposure and epidemiologic studies that
have become available in the last 20
years. Thus, the EPA considers it
appropriate to consider scientific
evidence for these purposes beyond the
scope of the ISA. More details on these
proposed revisions to the AQI are
provided below.
Although revisions of the air quality
criteria and NAAQS for PM generally
prompt changes to the AQI, the AQI is
not part of the NAAQS. The AQI is
aimed at communicating risks of
ambient concentrations which may far
exceed the level of the NAAQS. While
the AQI was not originally developed to
be used as a regulatory tool or for other
purposes and EPA does not provide
guidance on the use of the AQI for such
purposes, the EPA acknowledges that
some organizations and entities have
identified other uses for the AQI.110 As
such, the EPA is requesting information
about how other organizations and
entities are applying the AQI. The EPA’s
goal is to update the PM2.5 AQI in
conjunction with the Agency’s final
decisions on the primary annual and 24hour PM2.5 standards, if proposed
revisions to such standards are
promulgated.
1. Air Quality Index Values of 50, 100
and 150
With respect to the lower AQI
breakpoints, the EPA concludes that it
is still appropriate to continue to set
these breakpoints to be consistent with
the primary annual and 24-hour PM2.5
standard levels. The lowest AQI value of
110 For example, the Occupational Safety and
Health divisions in California, Oregon, and
Washington have linked outdoor worker regulations
to the upper AQI breakpoints.
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50 provides the breakpoint between the
‘‘good’’ and ‘‘moderate’’ categories. At
and below this concentration, air quality
is considered ‘‘good’’ for everyone.
Above this concentration, in the
‘‘moderate’’ category, the AQI contains
advisories for unusually sensitive
individuals. The EPA has historically
set this breakpoint at the level of the
primary annual PM2.5 standard. In doing
so, the EPA has recognized that: (1) the
annual standard is set to provide
protection to the public, including atrisk populations, from PM2.5
concentrations which, when
experienced on average for a year, have
the potential to result in adverse health
effects; and that (2) the AQI exposure
period represents a shorter exposure
period (e.g., 24-hour (or less)) while
focusing on the most sensitive
individuals. The EPA sees no basis for
deviating from this approach in this
reconsideration. Thus, the EPA
proposes to set the AQI value of 50 at
a daily (i.e., 24-hour) average
concentration equal to the level of the
primary annual PM2.5 standard that is
promulgated. In this document, the EPA
is proposing to revise the primary
annual PM2.5 standard level to 9 to 10
mg/m3 and soliciting comments on
levels down to 8 mg/m3 and up to 11 mg/
m3 (section II.D.3.a).
The historical approach to setting an
AQI value of 100, which is the
breakpoint between the ‘‘moderate’’ and
‘‘unhealthy for sensitive groups’’
categories, and above which advisories
are generated for sensitive groups, is to
set it at the same level as the primary
24-hour PM2.5 standard. In so doing, the
EPA has recognized that the primary 24hour PM2.5 standard is set to provide
protection to the public, including atrisk populations, from short-term
exposures to PM2.5 concentrations
which have the potential to result in
adverse health effects. Given this, it is
appropriate to generate advisories for
sensitive groups at concentrations above
this level. In the past, state, local, and
Tribal air quality agencies have
expressed strong support for this
approach (78 FR 3086, January 15,
2013). The EPA sees no basis to deviate
from this approach in this
reconsideration. In this proposal, the
EPA is proposing to retain the current
primary 24-hour PM2.5 standard with its
level of 35 mg/m3 but is taking comment
on revising the level of that standard to
25 mg/m3 (section II.D.3.b). Thus, the
EPA proposes to retain the AQI value of
100 set at the level of the current
primary 24-hour PM2.5 standard
concentration of 35 mg/m3 (i.e., 24-hour
average), but if the level of the 24-hour
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standard is revised to a different
concentration, the EPA is proposing to
set the final AQI value of 100 equal to
any revised level of the primary 24-hour
PM2.5 standard.
With respect to an AQI value of 150,
which is the breakpoint between the
‘‘unhealthy for sensitive groups’’ and
‘‘unhealthy categories,’’ this breakpoint
concentration in this reconsideration is
based upon the considering the same
health effects information, as assessed
in the 2019 ISA and ISA Supplement
and described in section II above, that
informs the proposed decisions on the
level of the 24-hour standard and the
AQI value of 100. Previously, the
Agency has used a proportional
adjustment in which the AQI value of
150 was set proportionally to the AQI
value of 100. This proportional
adjustment inherently recognizes that
the available epidemiologic studies
provide no evidence of discernible
thresholds, below which effects do not
occur in either sensitive groups or in the
general population, that could inform
conclusions regarding concentrations at
which to set this breakpoint. Given that
the epidemiologic evidence continues to
be the most relevant health effects
evidence for informing this range of AQI
values, the EPA sees no basis to deviate
from this approach in this
reconsideration. Therefore, the EPA
proposes to set an AQI value of 150
proportionally, depending on the
breakpoint concentration of the AQI
value of 100. This means that if the EPA
retains the current primary 24-hour
PM2.5 standard of 35 mg/m3, we propose
to also retain the current AQI value of
150 at a daily (i.e., 24-hour average)
concentration of 55 mg/m3. If, however,
the EPA revises the level of the primary
24-hour PM2.5 standard, we propose to
adjust the AQI value of 150 proportional
to that revision (e.g., a 24-hour standard
of 30 mg/m3 might result in an AQI
value for 150 of 45 mg/m3).
2. Air Quality Index Values of 200 and
Above
In 1999, the EPA established AQI
breakpoints for the AQI values of 200
and above (64 FR 42530, August 4,
1999). For this approach the AQI values
between 100 and 500 were based on
PM2.5 concentrations that generally
reflected a linear relationship between
increasing index values and increasing
PM2.5 concentrations.111 It was found
that this linear relationship was
generally consistent with the health
111 The AQI breakpoint at 150 was originally set
in 1999 to be linearly related to the concentrations
at the 100 and 500 breakpoints but then revised in
2012 to be proportional to the AQI breakpoint
concentration at 100 (78 FR 3181, January 15, 2013).
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effect evidence, which suggested that as
PM2.5 concentrations increase,
increasingly larger numbers of people
are likely to experience serious health
effects in this range of PM2.5
concentrations (64 FR 42536, August 4,
1999). For the AQI breakpoint of 500,
the concentration was based on the
method used to establish a previously
existing PM10 breakpoint that was
informed by studies conducted in
London using the British Smoke
method, which uses a different particle
size cutpoint.112 Due to limited ambient
PM2.5 monitoring data available at that
time, the decision on the 500 breakpoint
concentration for PM2.5 was based on
the stated assumption that PM
concentrations measured by the British
Smoke method were approximately
equivalent to PM2.5 concentrations (64
FR 42530, August 4, 1999). However,
the assumption of approximate
equivalence between the British Smoke
method and the current PM2.5
monitoring method is not consistent
with the view cited in the 1987 Federal
Register document about the PM10 AQI
value of 500, in which the British
Smoke method was noted to have a
particle size cutpoint of 4.5 microns (52
FR 24688, July 1, 1987). Given that the
British Smoke method has a larger
particle size cutpoint than the current
PM2.5 monitoring method which has a
cutpoint of 2.5 microns, a concentration
of 500 mg/m3 based on the British
Smoke method would be equivalent to
a lower PM2.5 concentration.
As part of this reconsideration, the
EPA recognizes that the health effects
evidence associated with PM2.5
exposure has greatly expanded in recent
years. While many of the new studies
evaluated in the 2019 ISA focused on
examining health effects associated with
exposure to lower PM2.5 concentrations,
there are also several new studies,
112 The current AQI value of 500 for PM
10 was set
in 1987 at the concentration of 600 mg/m3 based on
a 24-hour average, on the basis of increased
mortality associated with historical wintertime
pollution episodes in London (52 FR 24687 to
24688, July 1, 1987). Particle concentrations during
these episodes, measured by the British Smoke
method, were in the range of 500 to 1000 mg/m3.
In the 1987 rulemaking that established the upper
bound index value for PM10, the EPA cited a
generally held opinion that the British Smoke
method measures PM with a cutpoint of
approximately 4.5 microns (52 FR 24688, July 1,
1987). In establishing this value for PM10, the EPA
assumed that concentrations of PM10, which
includes both coarse (PM10–2.5) and fine particles
(PM2.5), during episodes of concern, would be about
100 mg/m3 higher than the PM concentration
measured in terms of British Smoke (52 FR 24688,
July 1, 1987). The PM10 upper bound index value
of 600 mg/m3 was developed by selecting the lower
end of the range of concentrations during the
historical wintertime pollution episodes in London
(500 mg/m3) and adding a margin of 100 mg/m3 to
account for this measurement difference.
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specifically controlled human exposure
studies, that can provide information
about health effects at concentrations
well above the standard levels.
Additionally, there are also studies now
available and evaluated in other Agency
documents that can inform health
effects at higher PM2.5 concentrations.
Thus, the EPA concludes that it is
appropriate to reevaluate the upper AQI
breakpoints, taking into account the
expanded body of scientific evidence. In
particular, because these breakpoints
were established in 1999 (64 FR 42530,
August 4, 1999), several new
epidemiologic studies have become
available that provide information about
exposures during high pollution events,
such as wildfires. Additionally,
multiple controlled human exposure
studies have become available that
provide information about health effects
across a range of concentrations. While
it remains unclear the exact PM2.5
concentrations at which specific health
effects occur, the more recent studies do
provide more refined information about
the concentration range in which these
effects might occur. For example, while
human exposure studies generally
report only subclinical effects, the
consistent observation of these effects in
multiple studies can provide an
indication of subclinical effects that are
on the pathway to more serious health
effects as PM2.5 concentrations increase
above 55 mg/m3. These studies provide
support for coherence of effects across
scientific disciplines and potentially
biologically plausible pathways for the
overt population-level health effects
observed in epidemiologic studies.
Therefore, taking into account the short
exposure time period in these studies
(e.g., 1–6 hours) and that the studies
generally do not include at-risk (or
sensitive) populations, but rather young,
healthy adults, these studies, in
conjunction with information from
epidemiologic studies, the EPA
preliminarily concludes it would be
appropriate to be more cautionary and
offer advisories to the public for
reducing exposures at lower
concentrations than recommended with
the current AQI breakpoints. Thus, the
discussion below focuses on the EPA’s
proposed revisions to the AQI
breakpoints of 200 and above and the
EPA’s interpretation of the available
health effects evidence that supports
those proposed revisions.
The AQI value of 200 is the
breakpoint between the ‘‘unhealthy’’
and ‘‘very unhealthy’’ categories. At
AQI values above 200, the AQI would
be providing a health warning that the
risk of anyone experiencing a health
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effect following short-term exposures to
these PM2.5 concentrations has
increased. To inform proposed
decisions on this breakpoint, the EPA
takes note of studies indicating the
potential for respiratory or
cardiovascular effects that are associated
with more serious health outcomes (e.g.,
emergency department visits, hospital
admissions). The controlled human
exposure studies evaluated in the 2009
and 2019 ISAs provide evidence of
inflammation as well as cardiovascular
effects in healthy subjects at and above
120 mg/m3. For example, Ramanathan et
al. (2016) observed a transient reduction
in antioxidant/anti-inflammatory
function after exposing healthy young
subjects to a mean concentration of 150
mg/m3 of PM2.5 for 2 hours. Urch et al.
(2010) also reported increased markers
of inflammation when exposing both
asthmatic and non-asthmatic subjects to
a mean concentration of 140 mg/m3 of
PM2.5 for 3 hours. In studies specifically
examining cardiovascular effects, Ghio
et al. (2000) and Ghio et al. (2003)
exposed healthy subjects to a mean
concentration of 120 mg/m3 for 2 hours
and reported significantly increased
levels of fibrinogen, a marker of
coagulation that increases during
inflammation. Sivagangabalan et al.
(2011) exposed healthy subjects to a
mean concentration of 150 mg/m3 of
PM2.5 for 2 hours and noted an
increased QT interval (3.4 ± 1.4)
indicating some evidence for
conduction abnormalities, an indicator
of possible arrhythmias. Lastly, Brook et
al. (2009) reported a transient increase
of 2.9 mm Hg in diastolic blood pressure
in healthy subjects during the 2-hour
exposure to a mean concentration of 148
mg/m3 of PM2.5.
In addition to epidemiologic studies
evaluated in the 2019 ISA that analyzed
exposures at ambient PM2.5
concentrations, there are a number of
recent epidemiologic studies focusing
on wildfire smoke that have become
available that were evaluated in the
EPA’s recently released peer-reviewed
assessment on wildland fire (U.S. EPA,
2021b). One of these studies,
Hutchinson et al. (2018), conducted a
bidirectional case-crossover analysis to
examine associations between wildfirespecific PM2.5 exposure and respiratoryrelated healthcare encounters (i.e., ED
visits, inpatient hospital admissions,
and outpatient visits) prior and during
the 2007 San Diego wildfires. This study
found positive and significant
associations to PM2.5 exposures and
respiratory-related healthcare
encounters. Further, during the initial 5day period of the wildfire event, the
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study observed that there was evidence
of increases in a number of respiratoryrelated outcomes particularly ED visits
for asthma, upper respiratory infection,
respiratory symptoms, acute bronchitis,
and all respiratory-related visits
(Hutchinson et al., 2018), giving the
EPA increased confidence in the
association between exposure to PM2.5
and respiratory-related outcomes at
concentrations experienced during this
time period. When examining the air
quality during the wildfire event, PM2.5
concentrations were highest during the
initial five days of the wildfire, with 24hour average PM2.5 concentrations of
89.1 mg/m3 across all zip codes and with
the highest 24-hour average of 160 mg/
m3 on the first day (Hutchinson et al.,
2018).
When considering this collective body
of evidence from controlled human
exposure and epidemiologic studies, the
Agency proposes to set an AQI value of
200 at a daily (i.e., 24-hour average)
concentration of PM2.5 of 125 mg/m3.
This concentration is at the lower end
of the concentrations consistently
shown to be associated with effects in
controlled human exposure studies
following short-term exposures (e.g., 2–
3 hours) and in young, healthy adults
(Ghio et al., 2000; Ghio et al., 2003;
Urch et al., 2010; Ramanathan et al.,
2016; Sivagangabalan et al., 2011; and
Brook et al., 2009) and also within the
range of 5-day average and maximum
concentrations observed to be associated
with respiratory-related outcomes
following exposure to wildfire smoke
(Hutchinson et al., 2018).
The AQI value of 300 denotes the
breakpoint between the ‘‘very
unhealthy’’ and ‘‘hazardous’’ categories,
and thus marks the beginning of the
‘‘hazardous’’ AQI category. At AQI
values above 300, the AQI provides a
health warning that everyone is likely to
experience effects following short-term
exposures to these PM2.5 concentrations.
To inform decisions on this AQI
breakpoint, the EPA takes note of
controlled human exposure studies that
consistently show subclinical effects
which are often associated with more
severe cardiovascular outcomes. As
discussed above, Brook et al. (2009)
reported a transient increase of 2.9 mm
Hg in diastolic blood pressure in
healthy subjects during the 2-hour
exposure to a mean concentration of 148
mg/m3 of PM2.5. Bellavia et al. (2013)
exposed healthy subjects to an average
PM2.5 concentration of 242 mg/m3 for 2
hours and reported increased systolic
blood pressure (2.53 mm Hg). Tong et al.
(2015) exposed healthy subjects to an
average PM2.5 concentration of 253 mg/
m3 for 2 hours and observed a
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significant increase in diastolic blood
pressure (2.1 mm Hg) and a
nonsignificant increase in systolic blood
pressure (2.5 mm Hg). Lucking et al.
(2011) reported impaired vascular
function and increased potential for
coagulation when exposing healthy
subjects to diesel exhaust (DE) with an
average PM2.5 concentration of 320 mg/
m3 for a duration of 1 hour.113 These
studies all provided evidence of
impaired vascular function, including
vasodilatation impairment and
increased thrombus formation, with
Tong et al. (2015), Bellavia et al. (2013),
Brook et al. (2009) all reporting
increases in blood pressure.
Additionally, Behbod et al. (2013)
reported increased inflammatory
markers following a 2-hour exposure to
an average PM2.5 concentration of 250
mg/m3 in healthy subjects.
In addition to the controlled human
exposure studies discussed above, the
epidemiologic study conducted by
DeFlorio-Barker et al. (2019) examined
the relationship between wildfire smoke
and cardiopulmonary hospitalizations
among adults 65 years of age and older
from 2008–2010 in 692 U.S. counties.
The authors reported a 2.22% increase
in all-cause respiratory hospitalizations
on wildfire smoke days for a 10 mg/m3
increase in 24-hour average PM2.5
concentrations (DeFlorio-Barker et al.,
2019). The maximum 24-hour average
concentration in this study on wildfire
smoke days was 212.5 mg/m3 (DeFlorioBarker et al., 2019). In considering this
study, the EPA notes the increased
probability that even healthy adults
experience effects at this maximum
exposure concentration, particularly
given that this maximum concentration
is near the exposure concentrations in
controlled human exposure studies that
consistently reported evidence of
impaired vascular function and several
that reported increases in blood
pressure in healthy adults following 2hour exposures.
Based on the information above, the
EPA proposes to revise the 300 level of
the AQI, which marks the beginning of
the ‘‘hazardous’’ AQI category, to a
concentration that is consistent with the
PM2.5 concentrations associated with
health effects as reported in the
controlled human exposure and
epidemiologic studies discussed above.
Specifically, the Agency proposes to set
an AQI value of 300 at a daily (i.e., 24hour average) PM2.5 concentration of
113 Although participants in Lucking et al. (2011)
were exposed to DE, the authors also conducted
analyses using a particle trap, and as noted in the
2019 ISA, this type of study design allows for the
assessment of the role of PM2.5 on the health effects
observed by removing PM from the DE mixture.
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225 mg/m3. This concentration falls
between the 2-hour average
concentrations reported in controlled
human exposure studies found to be
consistently associated, in healthy
adults, with impaired vascular function
and/or increases in blood pressure,
which can both be a precursor to more
severe cardiovascular effects following
short-term (1- to 2-hour) exposures, and
the maximum 24-hour average PM2.5
concentrations on wildfire smoke days
reported in the epidemiologic study
conducted by DeFlorio-Barker et al.
(2019).
Lastly, the EPA is also proposing
revisions to the 500 value of the AQI.
The 500 value of the AQI is within the
‘‘hazardous’’ category but is specified
and used to calculate the slope of the
AQI values in the ‘‘hazardous category’’
above and below AQI values of 500. In
the past, this breakpoint had a very
prominent role in determining the
current upper AQI values given that it
was used as part of the linear
relationship with the concentration at
the AQI value of 100 to determine the
AQI values of 200 and 300 in 1999 (64
FR 42530, August 4, 1999).
As discussed above, the current
breakpoint concentration for the 500
value of the AQI was set in 1999 at a
24-hour average PM2.5 concentration of
500 mg/m3 and was based on studies
conducted in London using the British
Smoke method, which used a different
particle size cutpoint and likely
overestimated the PM2.5 concentration.
In looking to improve upon that
approach, the EPA considers several
recent controlled human exposure
studies that observe health effects which
are clearly associated with more severe
cardiovascular outcomes and note that
these seem to follow exposures to high
PM2.5 concentrations that are well above
those typically observed in ambient air.
In controlled human exposure studies,
Vieira et al. (2016a) and Vieira et al.
(2016b) exposed healthy subjects and
subjects with heart failure to diesel
exhaust (DE) with a mean PM2.5
concentration of 325 mg/m3 for 21
minutes and reported decreased stroke
volume, and increased arterial stiffness
(an indicator of endothelial dysfunction)
in both healthy and heart failure
subjects.114 Also as discussed above,
Lucking et al. (2011) exposed healthy
subjects to DE with a mean PM2.5
concentration of 320 mg/m3 for 1
hour.115 The types of cardiovascular
effects observed in these controlled
human exposure studies have been
linked with the exacerbation of
ischemic heart disease (IHD) and heart
failure as well as myocardial infarction
(MI) and stroke.
In addition to the controlled human
exposure studies discussed above,
recent epidemiologic studies examining
the relationship between wildfire smoke
and respiratory health can also inform
proposed decisions on the concentration
for the AQI value of 500. As noted
earlier in this section, Hutchinson et al.
(2018) reported increases in a number of
respiratory-related outcomes
particularly ED visits for asthma, upper
respiratory infection, respiratory
symptoms, acute bronchitis, and all
respiratory-related visits during the
initial 5-day period of the 2007 San
Diego fire. During the initial 5-day
window, PM2.5 concentrations were
found to be at their highest with the
95th percentile of 24-hour average
concentrations of 333 mg/m3.
Although studies of short-term (i.e.,
daily) exposures to wildfire smoke are
more informative in considering
alternative level for the AQI value of
500 since they mirror the 24-hour
exposure timeframe, additional
information from epidemiologic studies
of longer-term exposures (i.e., over
many weeks) during wildfire events can
provide supporting information. For
example, Orr et al. (2020) conducted a
longitudinal study that examined
whether exposure to wildfire smoke
from a multi-month fire resulted in
respiratory effects in subsequent years.
The authors conducted respiratory
health assessments of adults living in
Seeley Lake and Thompson Falls, MT,
during the 3-month summer wildfire
event that occurred in 2017 as well as
follow-up visits in each of the two years
following the wildfire (Orr et al., 2020).
During the 2017 wildfire event (August
5641
1 to September 19, 2017), Orr et al.
(2020) reported that many days during
the multi-month fire had PM2.5
concentrations above 300 mg/m3,
resulting in a daily average PM2.5
concentration of 220.9 mg/m3 with a
maximum PM2.5 concentration of 638
mg/m3. This study included full
spirometry tests for all study
participants during the initial 2017 visit
and again in 2018 and 2019 to assess
lung function and reported that the
average FEV1/FVC (forced expiratory
volume in 1 second/forced vital
capacity) decreased significantly in
2018 (71.6% observed; 77.35%
predicted) and 2019 (73.4% observed;
76.52% predicted) (Orr et al., 2020).
This study suggests that exposure to
high PM2.5 concentrations during a
multi-week fire event may lead to longterm health consequences in the future,
such as declines in lung function.
The controlled human exposure
studies provide biological plausibility
for increases in respiratory-related
health care events during the wildfires
documented in epidemiologic studies.
The collective evidence from controlled
human exposure and epidemiologic
studies, which includes decreases in
stroke volume, increased arterial
stiffness, impaired vascular function
and respiratory-related healthcare
encounters provide health-based
evidence to inform proposed decisions
on the level of the AQI value of 500.
Given the concentrations observed in
these studies, the Agency proposes to
revise the AQI value of 500 to a level set
at a daily (i.e., 24-hour average) PM2.5
concentration of 325 mg/m3. This
concentration is at or below the lowest
concentrations observed in the
controlled human exposure studies
associated with more severe effects
discussed above and also at the low end
of the daily concentrations observed in
the epidemiologic studies conducted by
Hutchinson et al. (2018) and Orr et al.
(2020).
3. Summary
Table 1 below summarizes the
proposed breakpoints for the PM2.5 subindex.
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TABLE 1—PROPOSED BREAKPOINTS FOR PM2.5 SUB-INDEX
AQI category
Good ....................................................................................................................................
114 These effects were attenuated when the DE
was filtered, to reduce PM2.5 concentrations,
indicating the effects were likely associated with
PM2.5 exposure.
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115 When applying a particle trap, PM
2.5
concentrations were reduced, and effects associated
with cardiovascular function including impaired
vascular function, as measured by vasodilatation
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breakpoints
(μg/m3, 24hour average)
Index values
Frm 00085
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0–50
0.0–12.0
Proposed
breakpoints
(μg/m3, 24-hour
average)
0.0–(9.0–10.0)
and thrombus formation were attenuated indicating
associations with PM2.5.
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TABLE 1—PROPOSED BREAKPOINTS FOR PM2.5 SUB-INDEX—Continued
AQI category
Current
breakpoints
(μg/m3, 24hour average)
Index values
Moderate ..............................................................................................................................
Unhealthy for Sensitive Groups ...........................................................................................
Unhealthy .............................................................................................................................
Very Unhealthy ....................................................................................................................
Hazardous 1 .........................................................................................................................
51–100
101–150
151–200
201–300
301+
12.1–35.4
35.5–55.4
55.5–150.4
150.5–250.4
250.5
Proposed
breakpoints
(μg/m3, 24-hour
average)
(9.1–10.1)–35.4
35.5–55.4
55.5–125.4
125.5–225.4
225.5
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1 AQI values between breakpoints are calculated using equation 1 in appendix G. For AQI values in the hazardous category, AQI values greater than 500 should be calculated using equation 1 and the PM2.5 concentration specified for the AQI value of 500.
As discussed above, the EPA
recognizes that the health effects
evidence associated with PM2.5
exposure has greatly expanded in recent
years and concludes that the body of
scientific evidence supports the need to
revise many of the AQI breakpoints.
This is particularly true of the AQI
values of 200 and above, where the EPA
concludes that the available controlled
human exposure and epidemiologic
studies support offering advisories to
the public for reducing exposures at
lower concentrations than
recommended with the current AQI
breakpoints. However, the EPA also
recognizes that there are interpretations
and judgments that must be applied in
making the determinations of these
breakpoints. Thus, the EPA is soliciting
comment on the proposed revisions to
the AQI described above. In particular,
for the AQI values of 50, 100 and 150,
the EPA is soliciting comment on the
proposed decision to continue to use the
approach used in AQI revisions in 2012
(77 FR 38890, June 29, 2012) of setting
the lower breakpoints (50, 100, and 150)
to be consistent with the levels of the
primary annual and 24-hour PM2.5
standards and proposed decision to
revise the lower breakpoints to be
consistent with any changes to the
primary PM2.5 standards that are part of
this reconsideration. With respect to the
AQI values of 200 and above, the EPA
is soliciting comment on the proposed
decision to revise those AQI values, as
well as comment on the approach being
applied, the health studies viewed as
most relevant in these proposed
decisions, and the proposed AQI
breakpoint concentrations. The EPA
also notes that while the newer studies
do provide more refined information
about the concentration range in which
health effects might occur, the evidence
continues to support a continuum of
effects in concentration exposures in the
range of those defined by the upper AQI
values, with increasing PM2.5
concentrations being associated with
increasingly larger numbers of people
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likely experiencing serious health
effects. Given this, the EPA is also
soliciting comment on maintaining the
linear relationship approach used to set
the upper AQI values in 1999 but using
a different linear relationship (64 FR
42530, August 4, 1999). For example,
the EPA could set the AQI value of 150
based on the primary NAAQS and the
AQI value of 300 (which is the
breakpoint that identifies the starting
concentration for the highest AQI
category) based on the considerations
discussed above and using those values
to develop a linear relationship for the
AQI values for 200 and 500. Under this
approach, if the AQI breakpoint for 150
is set at 55.4 mg/m3 and the AQI
breakpoint for 300 is set at 225.4 mg/m3,
the AQI breakpoint for 200 would be
112.4 mg/m3 and the AQI breakpoint for
500 would be 452.4 mg/m3. The EPA
solicits comments on whether to use a
linear approach for higher breakpoints,
the appropriate breakpoints to use for
such an approach, and the appropriate
values for breakpoints under other
approaches, falling within the range of
the current breakpoints and the
breakpoints identified by these various
approaches, as well as to retain and not
change the existing breakpoints at this
time.
C. Air Quality Index Category
Breakpoints for PM10
The EPA proposes to retain the PM10
sub-index of the AQI consistent with the
proposed decision to retain the primary
PM10 standard, and consistent with the
health effects information that supports
this proposed decision, as discussed in
section III.D above.
D. Air Quality Index Reporting
With respect to the reporting
requirements for the AQI, there have
been many technological advances in air
quality monitoring and data reporting
since the appendix G to 40 CFR part 58
was last revised in 1999. Federal, state,
local, and Tribal agencies have used
these changes to make health
information and air quality data more
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readily available and easier to access.
Given this, it is useful to update the
reporting requirements and
recommendations to match current
practices and ensure the public has the
most useful and timely information to
take health-protective behaviors.
Currently, appendix G defines daily
reporting as five days per week. When
this reporting requirement was
originated in 1999 the technology
available at that time was not sufficient
to calculate and report the AQI more
than five days per week without
requiring additional staffing on the
weekends. Since that time, advances in
technology have allowed for reporting
seven days per week automatically
without expending additional resources
on weekends. As a result, most state,
local, and Tribal air agencies now report
the AQI seven days per a week. Given
these technological advances and noting
that reporting agencies currently report
the AQI seven days per week, the EPA
is proposing that state, local, and Tribal
agencies that report the AQI be required
to report it seven days a week, ensuring
that the public continues to have access
to daily air quality and health
information that they can use to take
steps to protect their health.
Improvements in monitoring
networks and modeling capabilities
have also enabled the ability to report
the AQI in near real-time. This allows
state, local, and Tribal air agencies to
provide timely air quality information to
the public for making health-protective
decisions and to help satisfy AQI
reporting requirements. The availability
of near real-time AQI data also allows
for more timely responses by the public
when air quality conditions are
changing rapidly, such as during
wildfire smoke events. Sub-daily
reporting of the AQI can be critical
when there are rapidly change
conditions and/or high pollution events
so that the public is able to make
informed decisions to protect their
health. Many state, local, and Tribal air
agencies currently report the AQI hourly
to ensure that the public has access to
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accurate and timely information. In
recognition of these advances, and to
continue to provide for near-real time
AQI reporting that the public has come
to rely on, the EPA proposes to
recommend that state, local, and Tribal
agencies report the AQI in near-real
time. Like air quality forecasting, which
also allows the public to make healthprotective, near-real time AQI reporting
is recommended but not required.
In lieu of or along with reporting the
near-real-time AQI directly to the
public, most state/local and Tribal
agencies submit hourly air quality data
to the EPA. The EPA uses this near-realtime data in the National, Interactive
and Fire and Smoke maps on the
AirNow website, and to create products
for use by weather service providers and
the media. Some state, local, and Tribal
air quality agencies also use these
products on their own websites and in
their own applications (i.e., the
California Air Resources Board uses the
data in its California Smoke Spotter
application). To continue to ensure the
availability of the products that the
public and many stakeholders rely
upon, the EPA is proposing to
recommend that state, local, and Tribal
air quality agencies submit hourly data
to the EPA’s air quality database.
Submitting hourly data to the EPA for
use on the AirNow website and in other
products also enables state, local, and
Tribal air quality agencies to meet the
recommendation to report the AQI in
near-real-time.
The Agency is updating the reporting
requirements and near-real-time
reporting and data submission
recommendations for the AQI. The
Agency is reformatting the questionand-answer format used in appendix G
to align with the current standard
formatting used in the Code of Federal
Regulations. The EPA is not taking
comment on or reopening the language
that has merely been moved or
rearranged as there are no substantive
changes.
Another change the EPA is proposing
to make to appendix G is with regard to
Table 2– Breakpoints for the AQI for
purposes of clarity. We are proposing to
collapse the two rows presented for the
Hazardous Category into one. The two
rows in the current table specify
pollutant concentrations for two AQI
ranges within the Hazardous category
(301–400 and 401–500), with an
intermediate break at 400. This
breakpoint of 400, along with those for
200 and 300, were defined and are the
historical basis for the Alert, Warning,
and Emergency episode levels included
in 40 CFR part 51, appendix L, as part
of the Prevention of Air Pollution
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Emergency Episodes program (44 FR 92,
May 10, 1979). The 400 breakpoint for
all criteria pollutants in the current
Table 2 is set at the proportional
pollutant concentration approximately
halfway between the index values of
300 and 500. In proposing updated AQI
breakpoints for PM2.5, the EPA
considered adjusting the 400 breakpoint
similarly. However, the EPA concluded
that collapsing the two rows into a
single range (301–500) would provide a
more transparent and easy-to-follow
presentation of the pollutant
concentrations corresponding to the
AQI range for the Hazardous category.
Moreover, collapsing the Hazardous
category into a single row in Table 2 has
no substantive effect on the Emergency
Episode program in 40 CFR part 51,
appendix L. Thus, the EPA is proposing
to remove the breakpoint of 400 from
the table in appendix G but this change
would not substantively affect the
derivation of the AQI for any pollutant.
In addition, the EPA plans to move
some information currently in appendix
G into the Technical Assistance
Document for the Reporting of Daily Air
Quality, or TAD (U.S. EPA, 2018a), so
that it can be updated in a more timely
manner to reflect current scientific and
health effects evidence and current
communication methods, thereby
assisting state, local, and Tribal agencies
in providing accurate and timely
information to the public. Information
that will be moved from appendix G to
the TAD includes the definitions of the
sensitive (at-risk) populations for each
pollutant. This definition is typically
evaluated and updated, as warranted, in
most NAAQS reviews, even if the
standard is not revised. Generally, if the
standard is not revised in a review of
the NAAQS, then appendix G is also not
revised. Moving the definitions of
sensitive groups to the TAD allows them
to be updated even when a NAAQS is
not revised to be consistent with the
definitions of the sensitive (at-risk)
populations identified in the ISA for a
NAAQS review. Data calculations for
non-required mathematical equations,
(i.e., the NowCast), are currently and
will continue to be included in the
TAD. The EPA works with state, local,
and Tribal air agencies to modify these
calculations as needed, which may not
be associated with a NAAQS review.
Also, recognizing that the ways that air
quality and health information is
supplied to the news media and public
changes regularly, information about
suggested approaches will be taken out
of appendix G and discussed in the
TAD.
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V. Rationale for Proposed Decisions on
the Secondary PM Standards
This section presents the rationale for
the Administrator’s proposed decision
that no change to the current secondary
PM standards is required at this time to
provide requisite protection against the
public welfare effects of PM within the
scope of this reconsideration (i.e.,
visibility, climate, and materials
effects).116 This rationale is based on a
thorough review of the scientific
evidence generally published through
December 2017,117 as presented in the
2019 ISA (U.S. EPA, 2019a), on the nonecological public welfare effects of PM
pertaining to the presence of PM in
ambient air, specifically visibility,
climate, and materials effects.
Additionally, this rationale is based on
a thorough evaluation of some studies
that became available after the literature
cutoff date of the 2019 ISA that could
either further inform the adequacy of
the current PM NAAQS or address key
scientific topics that have evolved since
the literature cutoff date for the 2019
ISA, generally through March 2021, as
presented in the ISA Supplement 118
(U.S. EPA, 2022a). The selection of
welfare effects evaluated within the ISA
Supplement was based on the causality
determinations reported in the 2019 ISA
and the subsequent use of scientific
116 Consistent with the 2016 Integrated Review
Plan (U.S. EPA, 2016), other welfare effects of PM,
such as ecological effects, are being considered in
the separate, on-going review of the secondary
NAAQS for oxides of nitrogen, oxides of sulfur and
PM. Accordingly, the public welfare protection
provided by the secondary PM standards against
ecological effects such as those related to deposition
of nitrogen- and sulfur-containing compounds in
vulnerable ecosystems is being considered in that
separate review. Thus, the Administrator’s
conclusion in this reconsideration of the 2020 final
decision will be focused only and specifically on
the adequacy of public welfare protection provided
by the secondary PM standards from effects related
to visibility, climate, and materials and hereafter
‘‘welfare effects’’ refers to non-ecological welfare
effects (i.e., visibility, climate, and materials
effects).
117 In addition to the 2020 review’s opening ‘‘call
for information’’ (79 FR 71764, December 3, 2014),
the 2019 ISA identified and evaluated studies and
reports that have undergone scientific peer review
and were published or accepted for publication
between January 1, 2009 through approximately
January 2018 (U.S. EPA, 2019a, p. ES–2). References
that are cited in the 2019 ISA, the references that
were considered for inclusion but not cited, and
electronic links to bibliographic information and
abstracts can be found at: https://hero.epa.gov/hero/
particulate-matter.
118 As described in more detail in the ISA
Supplement, ‘‘the scope of this Supplement
provides specific criteria for the types of studies
considered for inclusion within the Supplement.
Specifically, studies must be peer reviewed and
published between approximately January 2018 and
March 2021’’ (U.S. EPA, 2022a, section 1.2.2).
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evidence in the 2020 PA.119
Specifically, for welfare effects, the
focus within the ISA Supplement is on
visibility effects. The ISA Supplement
does not include an evaluation of
studies on climate or materials effects.
The Administrator’s rationale also takes
into account: (1) the PA evaluation of
the policy-relevant information in the
2019 ISA and ISA Supplement and
presentation of quantitative analysis of
air quality related to visibility
impairment; (2) CASAC advice and
recommendations, as reflected in
discussions of the drafts of the ISA
Supplement and PA at public meetings
and in the CASAC’s letters to the
Administrator; and (3) public comments
received during the development of
these documents.
In presenting the rationale for the
Administrator’s proposed decision and
its foundations, section V.A provides
background and introductory
information for this reconsideration of
the secondary PM standards. It includes
background on the 2020 final decision
to retain the secondary PM standards
(section V.A.1) and also describes the
general approach for this
reconsideration (section V.A.2). Section
V.B summarizes the key aspects of the
currently available evidence and
quantitative information for PM-related
visibility impairment and section V.C
summarizes the available information
for other PM-related welfare effects.
Section V.D presents the
Administrator’s proposed conclusions
on the current secondary PM standards
(V.D.III), drawing on both evidence- and
quantitative information-based
considerations (section V.D.1) and
advice from the CASAC (V.D.2).
119 As described in section 1.2.1 of the ISA
Supplement, ‘‘the selection of welfare effects to
evaluate within this Supplement is based on the
causality determinations reported in the 2019 PM
ISA and the subsequent use of scientific evidence
in the 2020 PM PA. The 2019 PM ISA concluded
a causal relationship for each of the welfare effects
categories evaluated (i.e., visibility, climate effects,
and materials effects). While the 2020 PM PA
considered the broader set of evidence for these
effects, for climate effects and material effects, it
concluded that there remained ‘substantial
uncertainties with regard to the quantitative
relationships with PM concentrations and
concentration patterns that limit[ed] [the] ability to
quantitatively assess the public welfare protection
provided by the standards from these effects (U.S.
EPA, 2020a). Given these uncertainties and
limitations, the basis of the discussion on
conclusions regarding the secondary standards in
the 2020 PM PA primarily focused on visibility
effects. Therefore, this Supplement focuses only on
visibility effects in evaluating newly available
scientific information and is limited to studies
conducted in the U.S. and Canada’’ (U.S. EPA,
2022a, section 1.2.1).
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A. General Approach
This reconsideration of the 2020 final
decision on the secondary PM standards
relies on the EPA’s assessments of the
current scientific evidence and
associated quantitative analyses to
inform the Administrator’s judgments
regarding secondary standards that are
requisite to protect the public welfare
from known or anticipated adverse
effects associated with the pollutant’s
presence in the ambient air. The EPA’s
assessments are primarily documented
in the 2019 ISA, ISA Supplement, and
PA, all of which have received CASAC
review and public comment (83 FR
53471, October 23, 2018; 83 FR 55529,
November 6, 2018; 85 FR 4655, January
27, 2020; 86 FR 52673, September 22,
2021; 86 FR 54186, September 30, 2021;
86 FR 56263, October 8, 2021; 87 FR
958, January 7, 2022; 87 FR 22207, April
14, 2022; 87 FR 31965, May 26, 2022).
In bridging the gap between the
scientific assessments of the 2019 ISA
and ISA Supplement and the judgments
required of the Administrator in
determining whether the current
standards provide the requisite public
welfare protection, the PA evaluates
policy implications of the evaluation of
the current evidence in the 2019 ISA
and ISA Supplement, and the
quantitative information documented in
the PA. In evaluating the public welfare
protection afforded by the current
standards against PM-related effects
within the scope of this reconsideration,
the four basic elements of the NAAQS
(indicator, averaging time, level, and
form) are considered collectively.
The final decision on the adequacy of
the current secondary standards is a
public welfare policy judgment to be
made by the Administrator. In reaching
conclusions with regard to the standard,
the decision will draw on the scientific
information and analyses about welfare
effects, and associated public welfare
significance, as well as judgments about
how to consider the range and
magnitude of uncertainties that are
inherent in the scientific evidence and
analyses. This approach is based on the
recognition that the available evidence
generally reflects a continuum that
includes ambient air exposures at which
scientists agree that effects are likely to
occur through lower levels at which the
likelihood and magnitude of responses
become increasingly uncertain. This
approach is consistent with the
requirements of the provisions of the
Clean Air Act related to the review of
NAAQS and with how the EPA and the
courts have historically interpreted the
Act. These provisions require the
Administrator to establish secondary
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standards that, in the judgment of the
Administrator, are requisite to protect
public welfare from known or
anticipated adverse effects associated
with the presence of the pollutant in the
ambient air. In so doing, the
Administrator seeks to establish
standards that are neither more nor less
stringent than necessary for this
purpose. The Act does not require that
standards be set at a zero-risk level, but
rather at a level that reduces risk
sufficiently so as to protect the public
welfare from known or anticipated
adverse effects.
The subsections below provide
background and introductory
information. Background on the 2020
decision to retain the current standards,
including the rationale for that decision,
for non-visibility effects and visibility
effects is summarized in sections
V.A.1.a and V.A.1.b below, respectively.
This is followed, in section V.A.2, by an
overview of the general approach for the
reconsideration of the 2020 final
decision. Following this introductory
section and subsections, the subsequent
sections summarize current information
and analyses, including that newly
available in this reconsideration. The
Administrator’s proposed conclusions
on the secondary PM standards, based
on the current information, are provided
in section V.D.3.
1. Background on the Current Standards
The current secondary PM standards
were affirmed in 2020 based on the
scientific and technical information
available at that time, as well as the
Administrator’s judgments regarding the
available welfare effects evidence, the
appropriate degree of public welfare
protection for the existing standards,
and available air quality information on
visibility impairment that may be
allowed by such a standard (85 FR
82684, December 18, 2020). With the
2020 decision, the Administrator
retained the secondary 24-hour PM2.5
standard, with its level of 35 mg/m3, the
annual PM2.5 standard, with its level of
15.0 mg/m3, and the 24-hour PM10
standard, with its level of 150 mg/m3.
The subsections below focus on the key
considerations, and the Administrator’s
conclusions, for climate and materials
effects (section V.A.1.a) and visibility
effects (section V.A.2.b) in the 2020
review.
a. Non-Visibility Effects
In light of the robust evidence base,
the 2019 ISA concluded there to be
causal relationships between PM and
climate effects and materials effects
(U.S. EPA, 2019a, sections 13.3.9 and
13.4.2). The 2020 final decision was
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based on a thorough review in the 2019
ISA of the scientific information on PMinduced climate and materials effects.
The decision also took into account: (1)
assessments in the 2020 PA of the most
policy-relevant information in the 2019
ISA regarding evidence of adverse
effects of PM to climate and materials,
(2) uncertainties in the available
evidence to inform a quantitative
assessment of PM-related climate and
materials effects, (3) CASAC advice and
recommendations, and (4) public
comments received during the
development of these documents and on
the proposal document.
Consistent with the general approach
routinely employed in NAAQS reviews,
the initial consideration in the 2020
review of the secondary standards was
with regard to the adequacy of
protection provided by the existing
standards. Key aspects of the
consideration are summarized in section
V.A.1.a.i below.
i. Considerations Regarding Adequacy
of the Existing Standards for NonVisibility Effects in the 2020 Review
In considering non-visibility welfare
effects in the 2020 review, as discussed
above, the Administrator concluded
that, while it is important to maintain
an appropriate degree of control of fine
and coarse particles to address nonvisibility welfare effects, ‘‘it is generally
appropriate to retain the existing
standards and that there is insufficient
information to establish any distinct
secondary PM standards to address
climate and materials effects of PM’’ (85
FR 82744, December 18, 2020).
With regard to climate, the
Administrator recognized that there
were a number of improvements and
refinements to climate models since the
2012 review. However, while the
evidence continued to support a causal
relationship between PM and climate
effects, the Administrator noted that
significant limitations continued to exist
related to quantifying the contributions
of direct and indirect effects of PM and
PM components on climate forcing (U.S.
EPA, 2020a, sections 5.2.2.1.1 and 5.4).
He also recognized that the models
continued to exhibit considerable
variability in estimates of PM-related
climate impacts at regional scales (e.g.,
∼100 km) as compared to simulations at
global scales. Therefore, the resulting
uncertainty led the Administrator to
conclude that the available scientific
information in the 2020 review
remained insufficient to quantify
climate impacts associated with
particular concentrations of PM in
ambient air (U.S. EPA, 2020a, section
5.2.2.2.1) or to evaluate or consider a
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level of PM air quality in the U.S. to
protect against climate effects and that
there was insufficient information
available to base a national ambient
standard on climate impacts (85 FR
82744, December 18, 2020).
With regard to materials effects, the
Administrator noted that the evidence
available in the 2019 ISA continued to
support a causal relationship between
materials effects and PM deposition
(U.S. EPA, 2019a, section 13.4). He
recognized that the deposition of fine
and coarse particles to materials can
lead to physical damage and/or
impaired aesthetic qualities. Particles
can contribute to materials damage by
adding to the natural weathering
processes and by promoting the
corrosion of metals, the degradation of
building materials, and the weakening
of material components. While some
new information was available in the
2019 ISA, the information was from
studies primarily conducted outside of
the U.S. in areas where PM
concentrations in ambient air are higher
than those observed in the U.S. (U.S.
EPA, 2020a, section 13.4). Additionally,
the information assessed in the 2019
ISA did not support quantitative
analyses of PM-related materials effects
in the 2020 review (U.S. EPA, 2020a,
section 5.2.2.2.2). Given the limited
amount of information available and its
inherent uncertainties and limitations,
the Administrator concluded that he
was unable to relate soiling or damage
to specific levels of PM in ambient air
or to evaluate or consider a level of air
quality to protect against such materials
effects, and that there was insufficient
information available to support a
distinct national ambient standard
based on materials effects (85 FR 82744,
December 18, 2020).
In the 2020 review, the CASAC agreed
with the 2020 PA conclusions that,
while these effects are important, ‘‘the
available evidence does not call into
question the protection afforded by the
current secondary PM standards’’ and
recommended that the secondary
standards ‘‘should be retained’’ (Cox,
2019b, p. 3 of letter). In reaching a final
decision in the 2020 review, for all of
the reasons discussed above and
recognizing the CASAC conclusion that
the evidence provided support for
retaining the current secondary PM
standards, the Administrator concluded
that it was appropriate to retain the
existing secondary PM standards,
without revision. For climate and
materials effects, this conclusion
reflected his judgment that, although it
remains important to maintain
secondary PM2.5 and PM10 standards to
provide some degree of control over
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long- and short-term concentrations of
both fine and coarse particles, there was
insufficient information to establish
distinct secondary PM standards to
address non-visibility PM-related
welfare effects (85 FR 82744, December
18, 2020).
b. Visibility Effects
The 2019 ISA concluded that, ‘‘the
evidence is sufficient to conclude that a
causal relationship exists between PM
and visibility impairment’’ (U.S. EPA,
2019a, section 13.2.6). The 2020
decision on the adequacy of the
secondary standards with regard to
visibility effects was a public welfare
policy judgment made by the
Administrator, which drew upon the
available scientific evidence for PMrelated visibility effects and on analyses
of visibility impairment, as well as
judgments about the appropriate weight
to place on the range of uncertainties
inherent in the evidence and analyses.
The 2020 final decision was based on a
thorough review in the 2019 ISA of the
scientific information on PM-related
visibility effects. The decision also took
into account: (1) assessments in the
2020 PA of the most policy-relevant
information in the 2019 ISA regarding
evidence of adverse effects of PM on
visibility; (2) air quality analyses of the
PM2.5 visibility index and design values
based on the form and averaging time of
the existing secondary 24-hour PM2.5
standard; (3) CASAC advice and
recommendations; and (4) public
comments received during the
development of these documents and on
the 2020 proposal document.
Consistent with the general approach
routinely employed in NAAQS reviews,
the initial consideration in the 2020
review of the secondary PM standards
was with regard to the adequacy of the
protection provided by the then-existing
standards. Key aspects of that
consideration are summarized in section
V.A.1.b.i below.
i. Consideration Regarding the
Adequacy of the Existing Standards for
Visibility Effects in the 2020 Review
In considering the visibility effects in
the 2020 review, the Administrator
noted the long-standing body of
evidence for PM-related visibility
impairment. This evidence, which is
based on the fundamental relationship
between light extinction and PM mass,
demonstrated that ambient PM can
impair visibility in both urban and
remote areas, and had changed very
little since the 2012 review (U.S. EPA,
2019a, section 13.1; U.S. EPA, 2009a,
section 9.2.5). The evidence related to
public perception of visibility
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impairment was from studies from four
areas in North America.120 These
studies provided information to inform
our understanding of levels of visibility
impairment that the public judged to be
‘‘acceptable’’ (U.S. EPA, 2010a; 85 FR
24131, April 30, 2020). In considering
these public preference studies, the
Administrator noted that, as described
in the 2019 ISA, no new visibility
studies had been conducted in the U.S.
and there was little newly available
information with regard to acceptable
levels of visibility impairment in the
U.S. The Administrator recognized that
visibility impairment can have
implications for people’s enjoyment of
daily activities and their overall wellbeing, and therefore, considered the
degree to which the current secondary
standards protect against PM-related
visibility impairment.
Consistent with the 2012 review, in
the 2020 review, the Administrator first
concluded that a target level of
protection for a secondary PM standard
is most appropriately defined in terms
of a visibility index that directly takes
into account the factors (i.e., species
composition and relative humidity) that
influence the relationship between
PM2.5 in ambient air and PM-related
visibility impairment. In defining a
target level of protection, the
Administrator considered the specific
aspects of such an index, including the
appropriate indicator, averaging time,
form and level (78 FR 82742–82744,
December 18, 2020).
First, with regard to indicator, the
Administrator noted that in the 2012
review, the EPA used an index based on
estimates of light extinction by PM2.5
components calculated using an
adjusted version of the IMPROVE
algorithm, which allows the estimation
of the light extinction using routinely
monitored components of PM2.5 and
PM10–2.5, along with estimates of relative
humidity. The Administrator recognized
that, while there have been some
revisions to the IMPROVE algorithm
since the time of the 2012 review, our
fundamental understanding of the
relationship between PM in ambient air
and light extinction had changed little
and the various IMPROVE algorithms
120 Preference studies were available in four
urban areas. Three western preference studies were
available, including one in Denver, Colorado (Ely et
al., 1991), one in the lower Fraser River valley near
Vancouver, British Columbia, Canada (Pryor, 1996),
and one in Phoenix, Arizona (BBC Research &
Consulting, 2003). A pilot focus group study was
also conducted for Washington, DC (Abt Associates,
2001), and a replicate study with 26 participants
was also conducted for Washington, DC (Smith and
Howell, 2009). More details about these studies are
available in Appendix D of the 2022 PA (U.S. EPA,
2022b).
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appropriately reflected this relationship
across the U.S. In the absence of a
monitoring network for direct
measurement of light extinction, he
concluded that a calculated light
extinction indicator that utilizes the
IMPROVE algorithms continued to
provide a reasonable basis for defining
a target level of protection against PMrelated visibility impairment (78 FR
82742–82744, December 18, 2020).
In further defining the characteristics
of a visibility index, the Administrator
next considered the appropriate
averaging time, form, and level of the
index. Given the available scientific
information the review, and in
considering the CASAC’s advice and
public comments, the Administrator
concluded that, consistent with the
decision in the 2012 review, a visibility
index with a 24-hour averaging time and
a form based on the 3-year average of
annual 90th percentile values remained
reasonable. With regard to the averaging
time and form of such an index, the
Administrator noted analyses conducted
in the last review that demonstrated
relatively strong correlations between
24-hour and subdaily (i.e., 4-hour
average) PM2.5 light extinction (78 FR
3226, January 15, 2013), indicating that
a 24-hour averaging time is an
appropriate surrogate for the subdaily
time periods of the perception of PMrelated visibility impairment and the
relevant exposure periods for segments
of the viewing public. This decision in
the 2020 review also recognized that a
24-hour averaging time may be less
influenced by atypical conditions and/
or atypical instrument performance (78
FR 3226, January 15, 2013). The
Administrator recognized that there was
no new information to support updated
analyses of this nature, and therefore, he
believed these analyses continued to
provide support for consideration of a
24-hour averaging time for a visibility
index in this review. With regard to the
statistical form of the index, the
Administrator noted that, consistent
with the 2012 review: (1) a multi-year
percentile form offers greater stability
from the occasional effect of interannual
meteorological variability (78 FR 3198,
January 15, 2013; U.S. EPA, 2011, p. 4–
58); (2) a 90th percentile represents the
median of the distribution of the 20
percent worst visibility days, which are
targeted in Federal Class I areas by the
Regional Haze Program; and (3) public
preference studies did not provide
information to identify a different target
than that identified for Federal Class I
areas (U.S. EPA, 2011, p. 4–59).
Therefore, the Administrator judged that
a visibility index based on estimates of
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light extinction, with a 24-hour
averaging time and a 90th percentile
form, averaged over three years,
remained appropriate (78 FR 82742–
82744, December 18, 2020).
With regard to the level of a visibility
index, consistent with the 2012 review,
the Administrator judged that it was
appropriate to establish a target level of
protection of 30 deciviews (dv),121 122
reflecting the upper end of the range of
visibility impairment judged to be
acceptable by at least 50% of study
participants in the available public
preference studies (78 FR 3226, January
15, 2013). The 2011 PA identified a
range of levels from 20 to 30 dv based
on the responses in the public
preference studies available at that time
(U.S. EPA, 2011, section 4.3.4). At the
time of the 2012 review, the
Administrator noted a number of
uncertainties and limitations in public
preference studies, including the small
number of stated preference studies
available, the relatively small number of
study participants, the extent to which
the study participants may not be
representative of the broader study area
population in some of the studies, and
the variations in the specific materials
and methods used in each study. In
considering the available preference
studies, with their inherent
uncertainties and limitations, the prior
Administrator concluded that the
substantial degree of variability and
uncertainty in the public preference
studies should be reflected in a target
level of protection based on the upper
end of the range of candidate protection
levels (CPLs).
Given that there were no new
preference studies available in the 2020
review, the Administrator’s judgments
were based on the same studies, with
the same range of levels, available in the
2012 review. As identified in the 2020
PA (U.S. EPA, 2020a, section 5.5), there
were a number of limitations and
uncertainties associated with these
studies, including the following:
• Available studies may not represent
the full range of preferences for
visibility in the U.S. population,
particularly given the potential
variability in preferences based on the
conditions commonly encountered and
the scenes being viewed.
• Available preference studies were
conducted 15 to 30 years ago and may
121 Deciview (dv) refers to a scale for
characterizing visibility that is defined directly in
terms of light extinction. The deciview scale is
frequently used in the scientific and regulatory
literature on visibility.
122 For comparison, 20 dv, 25 dv, and 30 dv are
equivalent to 64, 112, and 191 megameters (Mm–1),
respectively.
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not accurately represent the current day
preferences of people in the U.S.
• The variety of methods used in the
preference studies may potentially
influence the responses as to what level
of impairment is deemed acceptable.
• Factors that are not captured in the
methods of the preference studies, such
as the time of day when light extinction
is the greatest or the frequency of
impairment episodes, may influence
people’s judgment on acceptable
visibility (U.S. EPA, 2020a, section
5.2.1.1).
Therefore, in considering the
scientific information, with its
uncertainties and limitations, as well as
public comments on the level of the
target level of protection against
visibility impairment, the Administrator
concluded that it was appropriate to
again use a level of 30 dv for the
visibility index (78 FR 82742–82744,
December 18, 2020).
Having concluded that the protection
provided by a standard defined in terms
of a PM2.5 visibility index, with a 24hour averaging time, and a 90th
percentile form, averaged over 3 years,
set at a level of 30 dv, was requisite to
protect public welfare with regard to
visual air quality, the Administrator
next considered the degree of protection
from visibility impairment afforded by
the existing suite of secondary PM
standards.
In this context, the Administrator
considered the updated analyses of
visibility impairment presented in the
2020 PA (U.S. EPA, 2020a, section
5.2.1.2), which reflected a number of
improvements since the 2012 review.
Specifically, the updated analyses
examined multiple versions of the
IMPROVE equation, including the
version incorporating revisions since
the time of the 2012 review. These
updated analyses provided a further
understanding of how variation in the
inputs to the algorithms affect the
estimates of light extinction (U.S. EPA,
2020a, Appendix D). Additionally, for a
subset of monitoring sites with available
PM10–2.5 data, the updated analyses
better characterized the influence of
coarse PM on light extinction than in
the 2012 review (U.S. EPA, 2020a,
section 5.2.1.2).
The results of the updated analyses in
the 2020 PA were consistent with those
from the 2012 review. Regardless of
which version of the IMPROVE equation
was used, the analyses demonstrated
that, based on 2015–2017 data, the 3year visibility metric was at or below
about 30 dv in all areas meeting the
current 24-hour PM2.5 standard, and
below 25 dv in most of those areas. In
locations with available PM10–2.5
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monitoring, which met both the current
24-hour secondary PM2.5 and PM10
standards, 3-year visibility index
metrics were at or below 30 dv
regardless of whether the coarse fraction
was included as an input to the
algorithm for estimating light extinction
(U.S. EPA, 2020a, section 5.2.1.2). While
the inclusion of the coarse fraction had
a relatively modest impact on the
estimates of light extinction, the
Administrator recognized the continued
importance of the PM10 standard given
the potential for larger impacts on light
extinction in areas with higher coarse
particle concentrations, which were not
included in the analyses in the 2020 PA
due to a lack of available data (U.S.
EPA, 2019a, section 13.2.4.1; U.S. EPA,
2020a, section 5.2.1.2). He noted that
the air quality analyses showed that all
areas meeting the existing 24-hour PM2.5
standard, with its level of 35 mg/m3, had
visual air quality at least as good as 30
dv, based on the visibility index. Thus,
the secondary 24-hour PM2.5 standard
would likely be controlling relative to a
24-hour visibility index set at a level of
30 dv. Additionally, areas would be
unlikely to exceed the target level of
protection for visibility of 30 dv without
also exceeding the existing secondary
24-hour PM2.5 standard. Thus, the
Administrator judged that the 24-hour
PM2.5 standard provided sufficient
protection in all areas against the effects
of visibility impairment, i.e., that the
existing 24-hour PM2.5 standard would
provide at least the target level of
protection for visual air quality of 30 dv
which he judged appropriate (78 FR
82742–82744, December 18, 2020).
2. General Approach and Key Issues in
This Reconsideration of the 2020 Final
Decision
To evaluate whether it is appropriate
to consider retaining the current
secondary PM standards, or whether
consideration of revision is appropriate,
the EPA has adopted an approach in
this reconsideration that builds upon
the general approach used in past
reviews and reflects the body of
evidence and information now
available. Accordingly, the approach in
this reconsideration takes into
consideration the approaches used in
past reviews, including the substantial
assessments and evaluations performed
in those reviews, and also takes into
account the more recent scientific
information and air quality data now
available to inform understanding of the
key policy-relevant issues in the
reconsideration. As summarized above,
the Administrator’s decisions in the
2020 review were based on an
integration of PM welfare effects
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information with the judgments on the
public welfare significance of key
effects, policy judgments as to when the
standard is requisite, consideration of
CASAC advice, and consideration of
public comments.
Similarly, in this reconsideration, we
draw on the current information from
studies of PM-related visibility effects,
quantitative analyses of PM-related
visibility impairment, and information
from studies of non-visibility welfare
effects. In so doing, we consider both
the information available at the time of
the 2012 and 2020 reviews and
information more recently available,
including that which has been critically
analyzed and characterized in the 2019
ISA and ISA Supplement 123 for
visibility, climate, and materials effects.
The evaluations in the PA, of the
potential implications of various aspects
of the scientific evidence in the 2019
ISA and ISA Supplement (building on
prior such assessments), augmented by
the quantitative air quality, exposure or
risk-based information, are also
considered along with the associated
uncertainties and limitations.
B. Overview of Welfare Effects Evidence
The information summarized here is
based on the scientific assessment of the
welfare effects evidence available in this
reconsideration; this assessment is
documented in the 2019 ISA and ISA
Supplement and its policy implications
are further discussed in the PA. While
the 2019 ISA provides the broad
scientific foundation for this
reconsideration, we recognize that
additional literature has become
available since the cutoff date of the
2019 ISA that expands the body of
evidence related to visibility effects that
can inform the Administrator’s
judgment on the adequacy of the current
secondary PM standards. As such, the
ISA Supplement builds on the
information in the 2019 ISA with a
targeted identification and evaluation of
new scientific information regarding
visibility effects. As described in the
ISA Supplement and the PA, the
selection of welfare effects to evaluate
123 As noted above and described in detail in
section 1.4.2 of the PA, the ISA Supplement focuses
on a thorough evaluation of some studies that
became available after the literature cutoff date of
the 2019 ISA that could either further inform the
adequacy of the current PM NAAQS or address key
scientific topics that have evolved since the
literature cutoff date for the 2019 ISA. The selection
of the welfare effects to evaluate within the ISA
Supplement were based on the causality
determinations reported in the 2019 ISA and the
subsequent use of scientific evidence in the 2020
PA. Specifically, for welfare effects, the focus
within the ISA Supplement is on visibility effects.
The ISA Supplement does not include an
evaluation of studies on climate or materials effects.
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within the ISA Supplement were based
on the causality determinations reported
in the 2019 ISA and the subsequent use
of scientific evidence in the 2020 PA
(U.S. EPA, 2019a, section 1.2; U.S. EPA,
2022a, section 1.4.2). The ISA
Supplement focuses on U.S. and
Canadian studies that provide new
information on public preferences for
visibility impairment and/or developed
new methodologies or conducted
quantitative analyses of light extinction
(U.S. EPA, 2022a, section 1.2). Such
studies of visibility effects and
quantitative relationships between
visibility impairment and PM in
ambient air were considered to be of
greatest utility in informing the
Administrator’s conclusions on the
adequacy of the current secondary PM
standards. The visibility effects
evidence presented within the 2019
ISA, along with the targeted
identification and evaluation of new
scientific information in the ISA
Supplement, provides the scientific
basis for the reconsideration of the 2020
final decision on the secondary PM
standards for visibility effects. For
climate and materials effects, the 2020
PA concluded that there were
substantial uncertainties associated with
the quantitative relationships with PM
concentrations and the concentration
patterns that limited the ability to
quantitatively assess the public welfare
protection provided by the standards
from these effects. Therefore, the
evaluation of the information related to
these effects draws heavily from the
2019 ISA and 2020 PA. The subsections
below briefly summarize the nature of
PM-related visibility (section V.B.1.a),
climate (section V.B.1.b), and materials
(section V.B.1.c) effects.
1. Nature of Effects
Visibility impairment can have
implications for people’s enjoyment of
daily activities and for their overall
sense of well-being (U.S. EPA, 2009a,
section 9.2). The strongest evidence for
PM-related visibility impairment comes
from the fundamental relationship
between light extinction and PM mass
(U.S. EPA, 2009a), which confirms a
well-established ‘‘causal relationship
exists between PM and visibility
impairment’’ (U.S. EPA, 2009a, p. 2–28).
Beyond its effects on visibility, the 2009
ISA also identified a causal relationship
‘‘between PM and climate effects,
including both direct effects of radiative
forcing and indirect effects that involve
cloud and feedbacks that influence
precipitation formation and cloud
lifetimes’’ (U.S. EPA, 2009a, p. 2–29).
The evidence also supports a causal
relationship between PM and effects on
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materials, including soiling effects and
materials damage (U.S. EPA, 2009a, p.
2–31).
The evidence available in this
reconsideration is consistent with the
evidence available at the time of the
2012 and 2020 reviews and supports the
conclusions of causal relationships
between PM and visibility, climate, and
materials effects (U.S. EPA, 2019a,
chapter 13). Evidence newly available in
this reconsideration augments the
previously available evidence of the
relationship between PM and visibility
impairment (U.S. EPA, 2019a, section
13.2; U.S. EPA, 2022a, section 4),
climate effects (U.S. EPA, 2019a, section
13.3), and materials effects (U.S. EPA,
2019a, section 13.4).
a. Visibility
Visibility refers to the visual quality
of a human’s view with respect to color
rendition and contrast definition. It is
the ability to perceive landscape form,
colors, and textures. Visibility involves
optical and psychophysical properties
involving human perception, judgment,
and interpretation. Light between the
observer and the object can be scattered
into or out of the sight path and
absorbed by PM or gases in the sight
path. Consistent with conclusions of
causality in the 2012 and 2020 reviews,
the 2019 ISA concludes that ‘‘the
evidence is sufficient to conclude that a
causal relationship exists between PM
and visibility impairment’’ (U.S. EPA,
2019a, section 13.2.6). These
conclusions are based on the strong and
consistent evidence that ambient PM
can impair visibility in both urban and
remote areas (U.S. EPA, 2019a, section
13.1; U.S. EPA, 2009a, section 9.2.5).
The fundamental relationship
between light extinction and PM mass,
and the EPA’s understanding of this
relationship, has changed little since the
2009 ISA (U.S. EPA, 2009a). The
combined effect of light scattering and
absorption by particles and gases is
characterized as light extinction, i.e., the
fraction of light that is scattered or
absorbed per unit of distance in the
atmosphere.124 Light extinction is
measured in units of 1/distance, which
is often expressed in the technical
literature as visibility per megameter
(abbreviated Mm–1). Higher values of
124 All particles scatter light and, although a
larger particle scatters more light than a similarly
shaped smaller particle of the same composition,
the light scattered per unit of mass is greatest for
particles with diameters from ∼0.3–1.0 mm (U.S.
EPA, 2009a, section 2.5.1; U.S. EPA, 2019a, section
13.2.1). Particles with hygroscopic components
(e.g., particulate sulfate and nitrate) contribute more
to light extinction at higher relative humidity than
at lower relative humidity because they change size
in the atmosphere in response to relative humidity.
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light extinction (usually given in units
of Mm–1 or dv) correspond to lower
visibility. When PM is present in the air,
its contribution to light extinction is
typically much greater than that of gases
(U.S. EPA, 2019a, section 13.2.1). The
impact of PM on light scattering
depends on particle size and
composition, as well as relative
humidity. All particles scatter light, as
described by the Mie theory, which
relates light scattering to particle size,
shape, and index of refraction (U.S.
EPA, 2019a, section 13.2.3; Mie, 1908,
Van de Hulst, 1981). Fine particles
scatter more light than coarse particles
on a per unit mass basis and include
sulfates, nitrates, organics, lightabsorbing carbon, and soil (Malm et al.,
1994). Hygroscopic particles like
ammonium sulfate, ammonium nitrate,
and sea salt increase in size as relative
humidity increases, leading to increased
light scattering (U.S. EPA, 2019a,
section 13.2.3).
As at the time of the 2012 and 2020
reviews, direct measurements of PM
light extinction, scattering, and
absorption continue to be considered
more accurate for quantifying visibility
than PM mass-based estimates because
measurements do not depend on
assumptions about particle
characteristics (e.g., size, shape, density,
component mixture, etc.) (U.S. EPA,
2019a, section 13.2.2.2). Measurements
of light extinction can be made with
high time resolution, allowing for
characterization of subdaily temporal
patterns of visibility impairment. A
number of measurement methods have
been used for visibility impairment (e.g.,
transmissometers, integrating
nephelometers, teleradiometers,
telephotometers, and photography and
photographic modeling), although each
of these methods has its own strengths
and limitations (U.S. EPA, 2019a, Table
13–1). While some recent research
confirms and adds to the body of
knowledge regarding direct
measurements as is described in the
2019 ISA and ISA Supplement, no
major new developments have been
made with these measurement methods
since prior reviews (U.S. EPA, 2019a,
section 13.2.2.2; U.S. EPA, 2022a,
section 4.2).
In the absence of a robust monitoring
network for the routine measurement of
light extinction across the U.S.,
estimation of light extinction based on
existing PM monitoring can be used.
The theoretical relationship between
light extinction and PM characteristics,
as derived from Mie theory (U.S. EPA,
2019a, Equation 13.5), can be used to
estimate light extinction by combining
mass scattering efficiencies of particles
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with particle concentrations (U.S. EPA,
2019a, section 13.2.3; U.S. EPA, 2009a,
sections 9.2.2.2 and 9.2.3.1). This
estimation of light extinction is
consistent with the method used in
previous reviews. The algorithm used to
estimate light extinction, known as the
IMPROVE algorithm,125 provides for the
estimation of light extinction (bext), in
units of Mm–1, using routinely
monitored components of fine (PM2.5)
and coarse (PM10–2.5) PM. Relative
humidity data are also needed to
estimate the contribution by liquid
water that is in solution with the
hygroscopic components of PM. To
estimate each component’s contribution
to light extinction, their concentrations
are multiplied by extinction coefficients
and are additionally multiplied by a
water growth factor that accounts for
their expansion with moisture. Both the
extinction efficiency coefficients and
water growth factors of the IMPROVE
algorithm have been developed by a
combination of empirical assessment
and theoretical calculation using
particle size distributions associated
with each of the major aerosol
components (U.S. EPA, 2019a, sections
13.2.3.1 and 13.2.3.3).
At the time of the 2012 review, two
versions of the IMPROVE algorithm
were available in the literature—the
original IMPROVE algorithm (Lowenthal
and Kumar, 2004, Malm and Hand,
2007, Ryan et al., 2005) and the revised
IMPROVE algorithm (Pitchford et al.,
2007). As described in detail in the PA
(U.S. EPA, 2022b, section 5.3.1.1) and
the 2019 ISA (U.S. EPA, 2019a, section
13.2.3), the algorithm has been further
evaluated and refined since the time of
the 2012 review (Lowenthal and Kumar,
2016), particularly for PM
characteristics and relative humidity in
remote areas. All three versions of the
IMPROVE algorithm were considered in
evaluating visibility impairment in this
reconsideration.
Consistent with the evidence
available at the time of the 2012 and
2020 reviews, our understanding of
public perception of visibility
impairment comes from visibility
preference studies conducted in four
areas in North America.126 The detailed
125 The algorithm is referred to as the IMPROVE
algorithm as it was developed specifically to use
monitoring data generated at IMPROVE network
sites and with equipment specifically designed to
support the IMPROVE program and was evaluated
using IMPROVE optical measurements at the subset
of monitoring sites that make those measurements
(Malm et al., 1994).
126 Preference studies were available in four
urban areas in the last review: Denver, Colorado
(Ely et al., 1991), Vancouver, British Columbia,
Canada (Pryor, 1996), Phoenix, Arizona (BBC
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methodology for these studies are
described in the PA (U.S. EPA, 2022b,
section 5.3.1.1), the 2019 ISA (U.S. EPA,
2019a), and the 2009 ISA (U.S. EPA,
2019a). In summary, the study
participants were queried regarding
multiple images that were either
photographs of the same location and
scenery that had been taken on different
days on which measured extinction data
were available or digitized photographs
onto which a uniform ‘‘haze’’ had been
superimposed. Results of the studies
indicated a wide range of judgments on
what study participants considered to
be acceptable visibility across the
different study areas, depending on the
setting depicted in each photograph.
Based on the results of the four cities,
a range encompassing the PM2.5
visibility index values from images that
were judged to be acceptable by at least
50 percent of study participants across
all four of the urban preference studies
was identified (U.S. EPA, 2010a, p. 4–
24; U.S. EPA, 2020a, Figure 5–2). Much
lower visibility (considerably more haze
resulting in higher values of light
extinction) was considered acceptable
in Washington, DC, than was in Denver,
and 30 dv reflected the level of
impairment that was determined to be
‘‘acceptable’’ by at least 50 percent of
study participants (78 FR 3226–3227,
January 15, 2013).
Since the completion of the 2009 and
2019 ISAs, there has been only one
public preference study that has become
available in the U.S. This study uses
images of the Grand Canyon, AZ,
described in the ISA Supplement (U.S.
EPA, 2022a). The Grand Canyon study,
conducted by Malm et al. (2019), has a
similar study design to that used in the
public preference studies discussed
above; however, there are several
important differences that make it
difficult to directly compare the results
of the Malm et al. (2019) study with
other public preference studies. As an
initial matter, the Grand Canyon study
was conducted in a Federal Class I area,
as opposed to in an urban area, with a
scene depicted in the photographs that
did not include urban features.127 We
recognize that public preferences with
respect to visibility in Federal Class 1
areas may well differ from visibility
preferences in urban areas and other
Research & Consulting, 2003), and Washington, DC
(Abt Associates, 2001; Smith and Howell, 2009).
127 The Grand Canyon study used a single scene
looking west down the canyon with a small
landscape feature of a 100-km-distant mountain
(Mount Trumbull), along with other closer
landscape features. The scenes presented in the
previously available visibility preference studies are
presented in more detail in Table D–9 in the PA
(U.S. EPA, 2022b, Appendix D).
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contexts, although there is currently a
lack of information to on such
questions. Further, the Malm et al.
(2019) study also used a much lower
range of superimposed ‘‘haze’’ than the
preference studies discussed above.128 It
is unclear whether the participant
preferences are a function in part of the
range of potential values presented,
such that the participant preferences for
the Grand Canyon were generally
lower129 than the other preference
studies in part because of the lower
range of superimposed ‘‘haze’’ for the
images in that study, or if their
preferences would vary if presented
with images with a range of
superimposed ‘‘haze’’ more comparable
to the levels used in the other studies
(i.e., more ‘‘haze’’ superimposed on the
images).
The Malm et al. (2019) study also
explored alternate methods for
evaluating ‘‘acceptable’’ levels of visual
air quality from the preference studies,
including the use of scene-specific
visibility indices as potential indicators
of visibility levels as perceived by the
observer (Malm et al., 2019). In addition
to measures of atmospheric haze, such
as atmospheric extinction, used in
previously available preference studies,
other indices for visual air quality
include color and achromatic contrast of
single landscape figures, average and
equivalent contrast of an entire scene,
edge detection algorithms such as the
Sobel index, and just-noticeable
difference or change indexes. The
results reported by Malm et al. (2019)
suggest that scene-dependent metrics,
such as contrast, may be useful alternate
predictors of preference levels
compared to universal metrics like light
extinction (U.S. EPA, 2022a, section
4.2.1). This is because extinction alone
is not a measure of ‘‘haze,’’ but of light
attenuation per unit distance, and
visible ‘‘haze’’ is dependent on both
light extinction and distance to a
landscape feature (U.S. EPA, 2022a,
section 4.2.1). However, there are very
few studies available that use scenedependent metrics (i.e., contrast) to
evaluate public preference information,
which makes it difficult to evaluate
128 The Grand Canyon study superimposed light
extinction ranging from 3 dv to 20 dv on the image
slides shown to participants compared to the
previously available preference studies. In those
studies, the visibility ranges presented were as low
as 9 dv and as high as 45 dv. The visibility ranges
presented in the previously available visibility
preference studies are described in more detail in
Table D–9 in the PA (U.S. EPA, 2022b, Appendix
D).
129 In the Grand Canyon study, the level of
impairment that was determined to be ‘‘acceptable’’
by at least 50 percent of study participants was 7
dv (Malm et al., 2019).
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them as an alternative to the light
extinction approach.
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The available evidence continues to
support the conclusion of a causal
relationship between PM and climate
effects (U.S. EPA, 2019a, section 13.3.9).
Since the 2012 review, climate impacts
have been extensively studied and
recent research reinforces and
strengthens the evidence evaluated in
the 2009 ISA. Recent evidence provides
greater specificity about the details of
radiative forcing effects 130 and
increases the understanding of
additional climate impacts driven by
PM radiative effects. The
Intergovernmental Panel on Climate
Change (IPCC) assesses the role of
anthropogenic activity in past and
future climate change, and since the
completion of the 2009 ISA, has issued
the Fifth IPCC Assessment Report (AR5;
IPCC, 2013) which summarizes any key
scientific advances in understanding the
climate effects of PM since the previous
report. As in the 2009 ISA, the 2019 ISA
draws substantially on the IPCC report
to summarize climate effects. As
discussed in more detail in the PA (U.S.
EPA, 2022b, section 5.3.2.1.1), the
general conclusions are similar between
the IPCC AR4 and AR5 reports with
regard to effects of PM on global
climate. Consistent with the evidence
available in the 2012 review, the key
components, including sulfate, nitrate,
organic carbon (OC), black carbon (BC),
and dust, that contribute to climate
processes vary in their reflectivity,
forcing efficiencies, and direction of
forcing. Since the completion of the
2009 ISA, the evidence base has
expanded with respect to the
mechanisms of climate responses and
feedbacks to PM radiative forcing;
however, the recently published
literature assessed in the 2019 ISA does
not reduce the considerable
uncertainties that continue to exist
related these mechanisms.
As described in the PA (U.S. EPA,
2022b, section 5.3.2.1.1), PM has a very
heterogeneous distribution globally and
patterns of forcing tend to correlate with
130 Radiative forcing (RF) for a given atmospheric
constituent is defined as the perturbation in net
radiative flux, at the tropopause (or the top of the
atmosphere) caused by that constituent, in watts per
square meter (Wm–2), after allowing for
temperatures in the stratosphere to adjust to the
perturbation but holding all other climate responses
constant, including surface and tropospheric
temperatures (Fiore et al., 2015; Myhre et al., 2013).
A positive forcing indicates net energy trapped in
the Earth system and suggests warming of the
Earth’s surface, whereas a negative forcing indicates
net loss of energy and suggests cooling (U.S. EPA,
2019a, section 13.3.2.2).
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PM loading, with the greatest forcings
centralized over continental regions.
The climate response to this PM forcing,
however, is more complicated since the
perturbation to one climate variable
(e.g., temperature, cloud cover,
precipitation) can lead to a cascade of
effects on other variables. While the
initial PM radiative forcing may be
concentrated regionally, the eventual
climate response can be much broader
spatially or be concentrated in remote
regions, and may be quite complex,
affecting multiple climate variables with
possible differences in the direction of
the forcing in different regions or for
different variables (U.S. EPA, 2019a,
section 13.3.6). The complex climate
system interactions lead to variation
among climate models, which have
suggested a range of factors which can
influence large-scale meteorological
processes and may affect temperature,
including local feedback effects
involving soil moisture and cloud cover,
changes in the hygroscopicity of the PM,
and interactions with clouds (U.S. EPA,
2019a, section 13.3.7). However, there
remains insufficient evidence to related
climate effects to specific PM levels in
ambient air or to establish a quantitative
relationship between PM and climate
effects, particularly at a regional scale.
Further research is needed to better
characterize the effects of PM on
regional climate in the U.S. before PM
climate effects can be quantified.
c. Materials
Consistent with the evidence assessed
in the 2009 ISA, the available evidence
continues to support the conclusion that
there is a causal relationship between
PM deposition and materials effects.
Effects of deposited PM, particularly
sulfates and nitrates, to materials
include both physical damage and
impaired aesthetic qualities, generally
involving soiling and/or corrosion (U.S.
EPA, 2019a, section 13.4.2). Because of
their electrolytic, hygroscopic, and
acidic properties and their ability to
sorb corrosive gases, particles contribute
to materials damage by adding to the
effects of natural weathering processes,
by potentially promoting or accelerating
the corrosion of metals, degradation of
painted surfaces, deterioration of
building materials, and weakening of
material components.131 There is a
131 As
discussed in the 2019 ISA (U.S. EPA,
2019a, section 13.4.1), corrosion typically involves
reactions of acidic PM (i.e., acidic sulfate or nitrate)
with material surfaces, but gases like SO2 and nitric
acid (HNO3) also contribute. Because ‘‘the impacts
of gaseous and particulate N and S wet deposition
cannot be clearly distinguished’’ (U.S. EPA, 2019a,
p. 13–1), the assessment of the evidence in the 2019
ISA considers the combined impacts.
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limited amount of recently available
data for consideration in this review
from studies primarily conducted
outside of the U.S. on buildings and
other items of cultural heritage.
However, these studies involved
concentrations of PM in ambient air
greater than those typically observed in
the U.S. (U.S. EPA, 2019a, section 13.4).
Building on the evidence available in
the 2009 ISA, and as described in detail
in the PA (U.S. EPA, 2022b, section
5.3.2.1.2) and in the 2019 ISA (U.S.
EPA, 2019a, section 13.4), research has
progressed on (1) the theoretical
understanding of soiling of items of
cultural heritage; (2) the quantification
of degradation rates and further
characterization of factors that influence
damage of stone materials; (3) materials
damage from PM components besides
sulfate and black carbon and
atmospheric gases besides SO2; (4)
methods for evaluating soiling of
materials by PM mixtures; (5) PMattributable damage to other materials,
including glass and photovoltaic panels;
(6) development of dose-response
relationships for soiling of building
materials; and (7) damage functions to
quantify material decay as a function of
pollutant type and load. While the
evidence of PM-related materials effects
has expanded somewhat since the
completion of the 2009 ISA, there
remains insufficient evidence to relate
soiling or damage to specific PM levels
in ambient air or to establish a
quantitative relationship between PM
and materials degradation. The recent
evidence assessed in the 2019 ISA is
generally similar to the evidence
available in the 2009 ISA, including
associated limitations and uncertainties
and a lack of evidence to inform
quantitative relationships between PM
and materials effects, therefore leading
to similar conclusions about the PMrelated effects on materials.
C. Summary of Air Quality and
Quantitative Information
Beyond the consideration of the
scientific evidence, as discussed in
section V.B above, quantitative analyses
of PM air quality, when available, can
also inform conclusions on the
adequacy of the public welfare
protection provided by the current
secondary PM standards.
1. Visibility Effects
In the 2012 and 2020 reviews,
quantitative analyses for PM-related
visibility effects focused on daily
visibility impairment, given the shortterm nature of PM-related visibility
effects. The evidence and information
available in this reconsideration
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continues to provide support for the
short-term (i.e., hourly or daily) nature
of PM-related visibility impairment. As
such, the quantitative analyses
presented in the PA continue to focus
on daily visibility impairment and
utilize a two-phase assessment approach
for visibility impairment, consistent
with the approaches taken in past
reviews. First, the PA considers the
appropriateness of the elements
(indicator, averaging time, form, and
level) of the visibility index for
providing protection against PM-related
visibility effects. Second, recent air
quality was used to evaluate the
relationship between the current
secondary 24-hour PM2.5 standard and
the visibility index. The information
available since the 2012 review includes
an updated equation for estimating light
extinction, summarized in the PA (U.S.
EPA, 2022b, section 5.3.1.1) and
described in the 2019 ISA (U.S. EPA,
2019a, section 13.2.3.3), as well as more
recent air monitoring data, that together
allow for development of an updated
assessment of PM-related visibility
impairment in study locations in the
U.S.
a. Target Level of Protection in Terms of
a PM2.5 Visibility Index
In evaluating the adequacy of the
current secondary PM standards, the PA
first evaluates the appropriateness of the
elements (indicator, averaging time,
form, and level) identified for a distinct
secondary standard to protect against
visibility effects. In previous reviews,
the visibility index was set at a level of
30 dv, with estimated light extinction as
the indicator, a 24-hour averaging time,
and a 90th percentile form, averaged
over three years.
With regard to an indicator for the
visibility index, the PA recognizes the
lack of availability of methods and an
established network for directly
measuring light extinction (U.S. EPA,
2022b, section 5.3.1.1). Therefore,
consistent with previous reviews, the
PA concludes that a visibility index
based on estimates of light extinction by
PM2.5 components derived from an
adjusted version of the original
IMPROVE algorithm to be the most
appropriate indicator for the visibility
index in this reconsideration. As
described in section 5.3.1.1 of the PA,
the IMPROVE algorithm estimates light
extinction using routinely monitored
components of PM2.5 and PM10–2.5, along
with estimates of relative humidity (U.S.
EPA, 2022b, section 5.3.1.1).
With regard to averaging time, the PA
notes that the evidence continues to
provide support for the short-term
nature of PM-related visibility effects.
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Given that there is no new information
available regarding the time periods
during which visibility impairment
occurs or public preferences related to
specific time periods for visibility
impairment, the PA concludes that it is
appropriate to continue to focus on
daily visibility impairment. In so doing,
the PA relies on analyses that were
conducted in the 2012 review that
showed relatively strong correlations
between 24-hour and sub-daily (i.e., 4hour average) PM2.5 light extinction that
indicated that a 24-hour averaging time
is an appropriate surrogate for the subdaily time periods relevant for visual
perception (U.S. EPA, 2011, Figures G–
4 and G–5; Frank, 2012). These analyses
continue to provide support for a 24hour averaging time for the visibility
index in this reconsideration. Consistent
with previous reviews, the PA also
notes that the 24-hour averaging time
may be less influenced by atypical
conditions and/or atypical instrument
performance than a sub-daily averaging
time (85 FR 82740, December 18, 2020;
78 FR 3226, January 15, 2013).
With regard to the form for the
visibility index, the available
information continues to provide
support for a 3-year average of annual
90th percentile values. Given that there
is no new information to inform
selection of an alternate form, as in
previous reviews, the PA notes that the
3-year average form provides stability
from the occasional effect of interannual meteorological variability that
can result in unusually high pollution
levels for a particular year (85 FR 82741,
December 18, 2020; 78 FR 3198, January
15, 2013; U.S. EPA, 2011, p. 4–58). In
so doing, the PA considers the
evaluation in the 2010 Urban-Focused
Visibility Assessment (UFVA) of three
different statistical forms: 90th, 95th,
and 98th percentiles (U.S. EPA, 2010a,
Chapter 4). In considering this
evaluation of statistical forms from the
2010 UFVA, consistent with the 2011
PA, the PA notes that the Regional Haze
Program targets the 20 percent most
impaired days for visibility
improvements in visual air quality in
Federal Class I areas and that the
median of the distribution of these 20
percent most impaired days would be
the 90th percentile. The 2011 PA also
noted that strategies that are
implemented so that 90 percent of days
would have visual air quality that is at
or below the level of the visibility index
would reasonably be expected to lead to
improvements in visual air quality for
the 20 percent most impaired days.
Additionally, as in the 2011 PA, the PA
recognizes that the available public
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preference studies do not address
frequency of occurrence of different
levels of visibility (U.S. EPA, 2022b,
section 5.3.1.2). Therefore, the analyses
and consideration for the form of a
visibility index from the 2011 PA
continue to provide support for a 90th
percentile form, averaged across three
years, in defining the characteristics of
a visibility index in this
reconsideration.
With regard to the level for the
visibility index, the PA recognizes that
there is an additional public preference
study (Malm et al., 2019) available in
this reconsideration. As noted above,
however, this study differs from the
previously available public preference
studies in several ways which makes it
difficult to integrate this newly available
study with the previously available
studies. Most significantly, this study
was evaluated public preferences for
visibility in the Grand Canyon, perhaps
the most notable Class I area in the
country for visibility purposes.
Therefore, the PA concludes that the
Grand Canyon study is not directly
comparable to the other available
preferences studies and public
preferences of visibility impairment in
the Malm et al. (2019) are not
appropriate to consider in identifying a
range of levels for the target level of
protection against visibility impairment
for this reconsideration of the secondary
PM NAAQS.
Therefore, the PA continues to rely on
the same studies 132 and the range of 20
to 30 dv identified from those studies in
previous reviews. With regard to
selecting the appropriate target level of
protection for visibility impairment
within this range, the PA notes that in
previous reviews, a level at the upper
end of the range (i.e., 30 dv) was
selected given the uncertainties and
limitations associated with the public
preference studies (U.S. EPA, 2022b,
section 5.3.1.1). However, the PA also
recognizes that (1) the degree of
protection provided by a secondary PM
NAAQS is not determined solely by any
one element of the standard but by all
elements (i.e., indicator, averaging time,
form, and level) being considered
together, and (2) decisions regarding the
adequacy of the current secondary
standards is a public welfare policy
judgment to be made by the
Administrator. As such, the
Administrator may judge that a target
132 As noted above, the available public
preference studies include those conducted in
Denver, Colorado (Ely et al., 1991), Vancouver,
British Columbia, Canada (Pryor, 1996), Phoenix,
Arizona (BBC Research & Consulting, 2003), and
Washington, DC (Abt Associates, 2001; Smith and
Howell, 2009).
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level of protection below the upper end
of the range (i.e., less than 30 dv) is
appropriate, depending on his public
welfare policy judgments, which draw
upon the available scientific evidence
for PM-related visibility effects and on
analyses of visibility impairment, as
well as judgments about the appropriate
weight to place on the range of
uncertainties inherent in the evidence
and analyses.
In considering the available public
preference studies, consistent with past
reviews, the PA concludes that it is
reasonable to consider a range of 20 to
30 dv for selecting a target level of
protection, including a high value of 30
dv, a midpoint value of 25 dv, and a low
value of 20 dv. A target level of
protection at or in the upper end of the
range would focus on the Washington,
DC, preference study results (Abt
Associates, 2001; Smith and Howell,
2009) which identified 30 dv as the
level of impairment that was
determined to be ‘‘acceptable’’ by at
least 50 percent of study participants.
The public preferences of visibility
impairment in the Washington, DC,
study are likely to be generally
representative of urban areas that do not
have valued scenic elements (e.g.,
mountains) in the distant background.
This would be more representative of
areas in the middle of the country and
many areas in the eastern U.S., as well
as possibly some areas in the western
U.S.
A target level of protection in the
middle of the range would be most
closely associated with the level of
impairment that was determined to be
‘‘acceptable’’ by at least 50 percent of
study participants in the Phoenix, AZ,
study (BBC Research & Consulting,
2003), which was 24.3 dv. This study,
while methodologically similar to the
other public preference studies,
included participants that were selected
as a representative sample of the
Phoenix area population 133 and used
computer-generated images to depict
specific uniform visibility impairment
conditions. This study yielded the best
results of the four public preference
studies in terms of the least noisy
preference results and the most
133 The other preference studies did not include
populations that were necessarily representative of
the population in the area for which the images
being judged. For example, in the Denver, CO,
study, participants were from intact groups (i.e.,
those who were meeting for other reasons) and were
asked to provide a period of time during a regularly
scheduled meeting to participate in the study (Ely
et al., 1991). As another example, in the British
Columbia, Canada, study, participants were
recruited from undergraduate and graduate students
enrolled in classes at the University of British
Columbia’s Department of Geography (Pryor, 1996).
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representative selection of participants.
Therefore, based on this study, the use
of 25 dv to represent a midpoint within
the range of target levels protection is
well supported.
A target level of protection at or just
above the lower end of the range would
focus on the Denver, CO, study, but may
not be as strongly supported as higher
levels within the range (Ely et al., 1991).
Older studies, such as those conducted
in Denver, CO (Ely et al., 1991), and
British Columbia, Canada (Pryor, 1996),
used photographs that were taken at
different times of the day and on
different days to capture a range of light
extinction levels needed for the
preference studies. Compared to studies
that used computer-generated images
(i.e., those in Phoenix, AZ, and
Washington, DC) there was more
variability in scene appearance in these
older studies that could affect
preference rating and includes
uncertainties associated with using
ambient measurements to represent
sight path-averaged light extinction
values rather than superimposing a
computer-generated amount of haze
onto the images. When using
photographs, the intrinsic appearance of
the scene can change due to
meteorological conditions (i.e., shadow
patterns and cloud conditions) and
spatial variations in ambient air quality
that can result in ambient light
extinction measurement not being
representative of the sight-path-averaged
light extinction. Computer-generated
images, such as those generated with
WinHaze, do not introduce such
uncertainties, as the same base
photograph is used (i.e., there is no
intrinsic change in scene appearance)
and the modeled haze that is
superimposed on the photograph is
determined based on uniform light
extinction throughout the scene.
In addition to differences in
preferences that may arise from
photographs versus computer-generated
images, urban visibility preference may
differ by location, and such differences
may arise from differences in the
cityscape scene that is depicted in the
images. These differences are related to
the perceived value of objects and
scenes that are included in the image, as
objects at a greater distance have a
greater sensitivity to perceived visibility
changes as light extinction is changed
compared to similar scenes with objects
at shorter distances. For example, a
person (regardless of their location)
evaluating visibility in an image with
more scenic elements such as
mountains or natural views may value
better visibility conditions in these
images compared to the same level of
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visibility impairment in an image that
only depicts urban features such as
buildings and roads. That is, if a person
was shown the same level of visibility
impairment in two images depicting
different scenes—one with mountains in
the background and urban features in
the foreground and one with no
mountains in the background and
nearby buildings in the image without
mountains in the distance—may find
the amount of haze to be unacceptable
in the image with the mountains in the
distance because of a greater perceived
value of viewing the mountains, while
finding the amount of haze to be
acceptable in the image with the
buildings because of a lesser value of
viewing the cityscape or an expectation
that such urban areas may generally
have higher levels of haze in general.
This is consistent when comparing the
differences between the Denver, CO,
study results (which found the 50%
acceptance criteria occurred at the best
visual air quality levels among the four
cities) and the Washington, DC, results
(which found the 50% acceptability
criteria occurred at the worst visual air
quality levels among the four cities).
These results may occur because the
most prominent and picturesque feature
of the cityscape of Denver is the visible
snow-covered mountains in the
distance, while the prominent and
picturesque features of the Washington,
DC, cityscape are buildings relatively
nearby without prominent and/or values
scenic features that are more distant.
Given these variabilities in preferences
it is unclear to what extent, the available
evidence provides strong support for a
target level of protection at the lower
end of the range. Future studies that
reduce sources of noisiness and
uncertainty in the results could provide
more information that would support
selection of a target level of protection
at or just above the lower end of the
range.
Taken together, the PA concludes that
available information continues to
support a visibility index with
estimated light extinction as the
indicator, a 24-hour averaging time, and
a 90th percentile form, averaged over
three years, with a level within the
range of 20 to 30 dv.
b. Relationship Between the PM2.5
Visibility Index and the Current
Secondary 24-Hour PM2.5 Standard
The PA presents quantitative analyses
based on recent air quality that evaluate
the relationship between recent air
quality and calculated light extinction.
As in previous reviews, these analyses
explored this relationship as an estimate
of visibility impairment in terms of the
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24-hour PM2.5 standard and the
visibility index. Generally, the results of
the updated analyses are similar to
those based on the data available at the
time of the 2012 and 2020 reviews (U.S.
EPA, 2022b, section 5.3.1.2). As
discussed in section V.C.1.a above, the
PA concludes that the available
evidence continues to support a
visibility index with estimated light
extinction as the indicator, a 24-hour
averaging time, and a 90th percentile
form, averaged over three years, with a
level within the range of 20 to 30 dv.
These analyses evaluate visibility
impairment in the U.S. under recent air
quality conditions, particularly those
conditions that meet the current
standards, and the relative influence of
various factors on light extinction.
Given the relationship of visibility with
short-term PM, we focus particularly on
the short-term PM standards.134
Compared to the 2012 review, updated
analyses incorporate several
refinements, including (1) the
evaluation of three versions of the
IMPROVE equation to calculate light
extinction (U.S. EPA, 2022b, Appendix
D, Equations D–1 through D–3) in order
to better understand the influence of
variability in equation inputs; 135 (2) the
use of 24-hour relative humidity data,
rather than monthly average relative
humidity as was used in the 2012
review (U.S. EPA, 2022b, section
5.3.1.2, Appendix D); and (3) the
inclusion of the coarse fraction in the
estimation of light extinction (U.S. EPA,
2022b, section 5.3.1.2, Appendix D).
134 The analyses presented in the PA focus on the
visibility index and the current secondary 24-hour
PM2.5 standard with a level of 35 mg/m3. However,
we recognize that all three secondary PM standards
influence the PM concentrations associated with
the air quality distribution. As noted in section
V.A.1 above, the current secondary PM standards
include the 24-hour PM2.5 standard, with its level
of 35 mg/m3, the annual PM2.5 standard, with its
level of 15.0 mg/m3, and the 24-hour PM10 standard,
with its level of 150 mg/m3. With regard to the
annual PM2.5 standard, we note that all 60 areas
included in the analyses meet the current secondary
annual PM standard (U.S. EPA, 2022b, Table D–7).
135 While the PM
2.5 monitoring network has an
increasing number of continuous FEM monitors
reporting hourly PM2.5 mass concentrations, there
continue to be data quality uncertainties associated
with providing hourly PM2.5 mass and component
measurements that could be input into IMPROVE
equation calculations for sub-daily visibility
impairment estimates. As detailed in the PA, there
are uncertainties associated with the precision and
bias of 24-hour PM2.5 measurements (U.S. EPA,
2022b, p. 2–18), as well as to the fractional
uncertainty associated with 24-hour PM component
measurements (U.S. EPA, 2022b, p. 2–21). Given
the uncertainties present when evaluating data
quality on a 24-hour basis, the uncertainty
associated with sub-daily measurements may be
even greater. Therefore, the inputs to these light
extinction calculations are based on 24-hour
average measurements of PM2.5 mass and
components, rather than sub-daily information.
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The analyses in the reconsideration are
updated from the 2012 and 2020
reviews and include 60 monitoring sites
that measure PM2.5 and PM10 and are
geographically distributed across the
U.S. in both urban and rural areas (U.S.
EPA, 2022b, Appendix D, Figure D–1).
When light extinction was calculated
using the revised IMPROVE equation, in
areas that meet the current 24-hour
PM2.5 standard for the 2017–2019 time
period, all sites have light extinction
estimates at or below 26 dv (U.S. EPA,
2022b, Figure 5–3). For the four
locations that exceed the current 24hour PM2.5 standard, light extinction
estimates range from 22 dv to 27 dv
(U.S. EPA, 2022b, Figure 5–3). These
findings are consistent with the findings
of the analyses using the same
IMPROVE equation in the 2012 review
with data from 102 sites with data from
2008–2010 and in the 2020 review with
data from 67 sites with data from 2015–
2017. The analyses presented in the PA
indicate similar findings to those from
the analyses in the 2012 and 2020
reviews, i.e., the updated quantitative
analysis shows that the 3-year visibility
metric was no higher than 30 dv 136 at
sites meeting the current secondary PM
standards, and at most such sites the 3year visibility index values are much
lower (e.g., an average of 20 dv across
the 60 sites).137
When light extinction was calculated
using the revised IMPROVE equation,138
the resulting 3-year visibility metrics are
nearly identical to light extinction
estimates calculated using the original
IMPROVE equation (U.S. EPA, 2022b,
Figure 5–4), but some sites are just
slightly higher. Using the revised
IMPROVE equation, for those sites that
meet the current 24-hour PM2.5
standard, the 3-year visibility metric is
at or below 26 dv. For the four locations
that exceed the current 24-hour PM2.5
standard, light extinction estimates
range from 22 dv to 29 dv (U.S. EPA,
2022b, Figure 5–4). These results are
similar to those for light extinction
calculated using the original IMPROVE
equation,139 and those from previous
reviews.
136 A 3-year visibility metric with a level of 30 dv
would be at the upper end of the range of levels
identified from the public preference studies.
137 When light extinction is calculated using the
original IMPROVE equation, all 60 sites have 3-year
visibility metrics below 30 dv, 58 sites are at or
below 25 dv, and 26 sites are at or below 20 dv (see
U.S. EPA, 2022b, Appendix D, Table D–3).
138 As described in more detail in the PA, the
revised IMPROVE equation divides PM components
into smaller and larger sizes of particles in PM2.5,
with separate mass scattering efficiencies and
hygroscopic growth functions for each size category
(U.S. EPA, 2022b, section 5.3.1.1).
139 When light extinction is calculated using the
revised IMPROVE equation, all 60 sites have 3-year
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When light extinction was calculated
using the refined equation from
Lowenthal and Kumar (2016), the
resulting 3-year visibility metrics are
slightly higher at all sites compared to
light extinction estimates calculated
using the original IMPROVE equation
(U.S. EPA, 2022b, Figure 5–5).140 These
higher estimates are to be expected,
given the higher OC multiplier included
in the IMPROVE equation from
Lowenthal and Kumar (2016), which
reflects the use of data from remote
areas with higher concentrations of
organic PM when validating the
equation. As such, it is important to
note that the Lowenthal and Kumar
(2016) version of the equation may
overestimate light extinction in nonremote areas, including the urban areas
in the updated analyses in this
reconsideration.
Nevertheless, when light extinction is
calculated using the Lowenthal and
Kumar (2016) equation for those sites
that meet the current 24-hour PM2.5
standard, the 3-year visibility metric is
generally at or below 28 dv. For those
sites that exceed the current 24-hour
PM2.5 standard, three of these sites have
a 3-year visibility metric ranging
between 26 dv and 30 dv, while one site
in Fresno, California that exceeds the
current 24-hour PM2.5 standard and has
a 3-year visibility index value of 32 dv
(compared to 29 dv when light
extinction is calculated with the original
IMPROVE equation) (see U.S. EPA,
2022b, Appendix D, Table D–3). At this
site, it is likely that the 3-year visibility
metric using the Lowenthal and Kumar
(2016) equation would be below 30 dv
if PM2.5 concentrations were reduced
such that the 24-hour PM2.5 level of 35
mg/m3 was attained.
In considering visibility impairment
under recent air quality conditions, the
PA recognizes that the differences in the
inputs to equations estimating light
extinction can influence the resulting
values. For example, given the varying
chemical composition of emissions from
different sources, the 2.1 multiplier in
the Lowenthal and Kumar (2016)
equation may not be appropriate for all
source types. At the time of the 2012
review, the EPA judged that a 1.6
multiplier for converting OC to organic
matter (OM) was more appropriate, for
visibility metrics below 30 dv, 56 sites are at or
below 25 dv, and 26 sites are at or below 20 dv (see
U.S. EPA, 2022b, Appendix D, Table D-3).
140 When light extinction is calculated using the
Lowenthal and Kumar IMPROVE equation, 59 sites
have 3-year visibility metrics below 30 dv, 45 sites
are at or below 25 dv, and 15 sites are at or below
20 dv. The one site with a 3-year visibility metric
of 32 dv exceeds the secondary 24-hour PM2.5
standard, with a design value of 56 mg/m3 (see U.S.
EPA, 2022b, Appendix D, Table D–3).
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the purposes of estimating visibility
index at sites across the U.S., than the
1.4 or 1.8 multipliers used in the
original and revised IMPROVE
equations, respectively. A multiplier of
1.8 or 2.1 would account for the more
aged and oxygenated organic PM that
tends to be found in more remote
regions than in urban regions, whereas
a multiplier of 1.4 may underestimate
the contribution of organic PM found in
remote regions when estimating light
extinction (78 FR 3206, January 15,
2013; U.S. EPA, 2012, p. IV–5). The
available scientific information and
results of the air quality analyses
indicate that it may be appropriate to
select inputs to the IMPROVE equation
(e.g., the multiplier for OC to OM) on a
regional basis rather than a national
basis when calculating light extinction.
This is especially true when comparing
sites with localized PM sources (such as
sites in urban or industrial areas) to sites
with PM derived largely from biogenic
precursor emissions (that contribute to
widespread secondary organic aerosol
formation), such as those in the
southeastern U.S. The PA notes,
however, that conditions involving PM
from such different sources have not
been well studied in the context of
applying a multiplier to estimate light
extinction, contributing uncertainty to
estimates of light extinction for such
conditions.
At the time of the 2012 review, the
EPA noted that PM2.5 is the size fraction
of PM responsible for most of the
visibility impairment in urban areas (77
FR 38980, June 29, 2012). Data available
at the time of the 2012 review suggested
that, generally, PM10–2.5 was a minor
contributor to visibility impairment
most of the time (U.S. EPA, 2010a)
although the coarse fraction may be a
major contributor in some areas in the
desert southwestern region of the U.S.
Moreover, at the time of the 2012
review, there were few data available
from PM10–2.5 monitors to quantify the
contribution of coarse PM to calculated
light extinction. Since that time, an
expansion in PM10–2.5 monitoring efforts
has increased the availability of data for
use in estimating light extinction with
both PM2.5 and PM10–2.5 concentrations
included as inputs in the equations. The
analysis in the 2020 review addressed
light extinction at 20 of the 67 PM2.5
sites where collocated PM10–2.5
monitoring data were available. Since
the 2020 review, PM10–2.5 monitoring
data are available at more locations and
the analyses presented in the PA
include those for light extinction
estimated with coarse and fine PM at all
60 sites. Generally, the contribution of
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the coarse fraction to light extinction at
these sites is minimal, contributing less
than 1 dv to the 3-year visibility metric
(U.S. EPA, 2020a, section 5.2.1.2).
However, the PA notes that in the
updated quantitative analyses, only a
few sites were in locations that would
be expected to have high concentrations
of coarse PM, such as the Southwest.
These results are consistent with those
in the analyses in the 2019 ISA, which
found that mass scattering from PM10–2.5
was relatively small (less than 10%) in
the eastern and northwestern U.S.,
whereas mass scattering was much
larger in the Southwest (more than 20%)
particularly in southern Arizona and
New Mexico (U.S. EPA, 2019a, section
13.2.4.1, p. 13–36).
Overall, the findings of these updated
quantitative analyses are generally
consistent with those in the 2012 and
2020 reviews. The 3-year visibility
metric was generally below 26 dv in
most areas that meet the current 24-hour
PM2.5 standard. Small differences in the
3-year visibility metric were observed
between the variations of the IMPROVE
equation, which may suggest that it may
be more appropriate to use one version
over another in different regions of the
U.S. based on PM characteristics such as
particle size and composition to more
accurately estimate light extinction.
2. Non-Visibility Effects
Consistent with the evidence
available at the time of the 2012 and
2020 reviews, and as described in detail
in the PA (U.S. EPA, 2022b, section
5.3.2.2), the data remain insufficient to
conduct quantitative analyses for PM
effects on climate and materials. For
PM-related climate effects, as explained
in more detail in the PA (U.S. EPA,
2022b, section 5.3.2.1.1), our
understanding of PM-related climate
effects is still limited by significant key
uncertainties. The recently available
evidence does not appreciably improve
our understanding of the spatial and
temporal heterogeneity of PM
components that contribute to climate
forcing (U.S. EPA, 2022b, sections
5.3.2.1.1 and 5.5). Significant
uncertainties also persist related to
quantifying the contributions of PM and
PM components to the direct and
indirect effects on climate forcing, such
as changes to the pattern of rainfall,
changes to wind patterns, and effects on
vertical mixing in the atmosphere (U.S.
EPA, 2022b, sections 5.3.2.1.1 and 5.5).
Additionally, while improvements have
been made to climate models since the
completion of the 2009 ISA, the models
continue to exhibit variability in
estimates of the PM-related climate
effects on regional scales (e.g., ∼100 km)
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compared to simulations at the global
scale (U.S. EPA, 2022b, sections
5.3.2.1.1 and 5.5). While our
understanding of climate forcing on a
global scale is somewhat expanded
since the 2012 review, significant
limitations remain to quantifying
potential adverse PM-related climate
effects in the U.S. and how they would
vary in response to incremental changes
in PM concentrations across the U.S. As
such, while recent research is available
on climate forcing on a global scale, the
remaining limitations and uncertainties
are significant, and the recent global
scale research does not translate directly
for use at regional spatial scales.
Therefore, the evidence does not
provide a clear understanding at the
necessary spatial scales for quantifying
the relationship between PM mass in
ambient air and the associated climaterelated effects in the U.S. that would be
necessary for informing consideration of
a national PM standard on climate in
this reconsideration (U.S. EPA, 2022b,
section 5.3.2.2.1; U.S. EPA, 2019a,
section 13.3).
For PM-related materials effects, as
explained in more detail in the PA (U.S.
EPA, 2022b, section 5.3.2.1.2), the
available evidence has been somewhat
expanded to include additional
information about the soiling process
and the types of materials impacted by
PM. This evidence provides some
limited information to inform doseresponse relationships and damage
functions associated with PM, although
most of these studies were conducted
outside of the U.S. where PM
concentrations in ambient air are
typically above those observed in the
U.S. (U.S. EPA, 2022b, section 5.3.2.1.2;
U.S. EPA, 2019a, section 13.4). The
evidence on materials effects
characterized in the 2019 ISA also
includes studies examining effects of
PM on the energy efficiency of solar
panels and passive cooling building
materials, although the evidence
remains insufficient to establish
quantitative relationships between PM
in ambient air and these or other
materials effects (U.S. EPA, 2022b,
section 5.3.2.1.2). While the available
evidence assessed in the 2019 ISA is
somewhat expanded since the time of
the 2012 review, quantitative
relationships have not been established
for PM-related soiling and corrosion and
frequency of cleaning or repair that
further the understanding of the public
welfare implications of materials effects
(U.S. EPA, 2022b, section 5.3.2.2.2; U.S.
EPA, 2019a, section 13.4). Therefore,
there is insufficient information to
inform quantitative analyses assessing
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materials effects to inform consideration
of a national PM standard on materials
in this reconsideration (U.S. EPA,
2022b, section 5.3.2.2.2; U.S. EPA,
2019a, section 13.4).
D. Proposed Conclusions on the
Secondary PM Standards
In reaching proposed conclusions on
the current secondary PM standards
(presented in section IV.D.3), the
Administrator has taken into account
policy-relevant evidence- and
quantitative information-based
considerations discussed in the PA
(summarized in section IV.D.2), as well
as advice from the CASAC and public
comment on the standards received thus
far in the reconsideration (section
IV.D.1). In general, the role of the PA is
to help ‘‘bridge the gap’’ between the
Agency’s assessment of the current
evidence and quantitative analyses, and
the judgments required of the
Administrator in determining whether it
is appropriate to retain or revise the
NAAQS. Evidence-based considerations
draw upon the EPA’s integrated
assessment of the scientific evidence of
PM-related welfare effects presented in
the 2019 ISA and ISA Supplement
(summarized in section V.B above) to
address key policy-relevant questions in
the reconsideration. Similarly, the
quantitative information-based
considerations (summarized in section
V.C above) focused on the potential for
PM-related welfare effects under recent
air quality conditions for the purposes
of addressing the policy-relevant
questions.
This approach to reviewing the
secondary standards is consistent with
the requirements of the provisions of the
CAA related to the review of the
NAAQS and with how the EPA and the
courts have historically interpreted the
CAA. As discussed in section I.A above,
these provisions require the
Administrator to establish secondary
standards that, in the Administrator’s
judgment, are requisite (i.e., neither
more nor less stringent than necessary)
to protect the public welfare from
known or anticipated adverse effects
associated with the presence of the
pollutant in ambient air. Consistent
with the Agency’s approach across all
NAAQS reviews, the EPA’s approach to
informing these judgments is based on
a recognition that the available welfare
effects evidence generally reflects a
continuum that includes ambient air
exposures for which scientists generally
agree that effects are likely to occur
through lower levels at which the
likelihood and magnitude of response
become increasingly uncertain. The
CAA does not require the Administrator
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to establish secondary standards at a
zero-risk level, but rather at a level that
reduces risk sufficiently so as to protect
the public welfare from known or
anticipated adverse effects.
The proposed decision on the
adequacy of the current secondary
standards described below is a public
welfare policy judgment by the
Administrator that draws upon the
scientific evidence for the relevant
welfare effects, quantitative analyses of
air quality, as available, and judgments
about how to consider the uncertainties
and limitations that are inherent in the
scientific evidence and quantitative
analyses. The four basic elements of the
NAAQS (i.e., indicator, averaging time,
form, and level) have been considered
collectively in evaluating the public
welfare protection afforded by the
current standard against PM-related
visibility, climate and materials effects.
The Administrator’s final decision will
additionally consider public comments
received on this proposed decision.
1. CASAC Advice in This
Reconsideration
The CASAC provided its advice
regarding the current secondary
standards in the context of its review of
the draft PA (Sheppard, 2022a).141 In its
comments on the draft PA, the CASAC
first recognized the scientific evidence
is sufficient to support a causal
relationship between PM and visibility
effects, climate effects and materials
effects.
With regard to visibility effects, the
CASAC recognized that the
identification of a target level of
protection for the visibility index is
based on a limited number of studies
and suggested that ‘‘additional regionand view-specific visibility preference
studies and data analyses are needed to
support a more refined visibility target’’
(Sheppard, 2022a, p. 21 of consensus
responses). While the CASAC did not
recommend revising either the target
level of protection for the visibility
index or the level of the current 24-hour
PM2.5 standard, they did state that a
visibility index of 30 deciviews ‘‘needs
141 A limited number of public comments have
also been received in this reconsideration to date,
including comments focused on the draft PA. Of
those public comments that addressed the adequacy
of the secondary PM standards, the majority of
commenters support the preliminary conclusion
that it is appropriate to consider retaining the
current secondary PM standards, without revision.
These commenters generally cite to a lack of newly
available evidence and information that would
inform consideration of alternative secondary PM
standards to protect against PM-related effects on
visibility, climate, and materials. One commenter,
however, supported the revision of the secondary
PM standards to provide additional protection
against PM-related visibility effects.
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to be justified’’ and ‘‘[i]f a value of 20–
25 deciviews is deemed to be an
appropriate visibility target level of
protection, then a secondary 24-hour
PM2.5 standard in the range of 25–35 mg/
m3 should be considered’’ (Sheppard,
2022a, p. 21 of consensus responses).
The CASAC also recognized the
limited availability of monitoring
methods and networks for directly
measuring light extinction. As such,
they suggest that ‘‘[a] more extensive
technical evaluation of the alternatives
for visibility indicators and practical
measurement methods (including the
necessity for a visibility FRM) is need
for future reviews’’ (Sheppard, 2022a, p.
22 of consensus letter). The majority of
the CASAC ‘‘recommend[ed] that an
FRM for a directly measured PM2.5 light
extinction indicator be developed’’ to
inform the consideration of the
protection afforded by the secondary
PM standards against visibility
impairment, the minority of the CASAC
‘‘believe that a light extinction FRM is
not necessary to set a secondary
standard protective of visibility’’
(Sheppard, 2022a, p. 22 of consensus
responses).
With regard to climate and materials
effects, the CASAC noted that
substantial uncertainties remain in the
scientific evidence for these effects. The
CASAC suggested a number of areas for
future research to further inform our
understanding of these effects,
including more climate-related research
and research that would allow for
quantitative assessment of the
relationship between materials effects
and PM in ambient air.
2. Evidence- and Quantitative
Information-Based Considerations in the
Policy Assessment
The secondary PM standards include
the 24-hour PM2.5 standard, with its
level of 35 mg/m3 as the 98th percentile,
averaged over three years; the annual
PM2.5 standard, with its level of 15.0 mg/
m3 as the annual mean, averaged over
three years; and the 24-hour PM10
standard, with its level of 150 mg/m3,
not to be exceeded more than once per
year on average over three years.
Together, these standards provide
protection against both long-term
average and short-term peak PM
concentrations. For example, the 24hour PM2.5 standard is most effective at
limiting peak 24-hour PM2.5
concentrations, but in doing so, also has
an effect on annual average PM2.5
concentrations. Additionally, the annual
standard is most effective in controlling
‘‘typical’’ or average PM2.5
concentrations, but also provides some
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measure of protection against peak
exposures.
The PA considers the degree to which
the available scientific evidence and
quantitative information supports or
calls into question the adequacy of the
protection afforded by the current
secondary PM standards. In doing so,
the PA considers the evidence assessed
in the 2019 ISA and ISA Supplement,
including the extent to which the
evidence for PM-related visibility
impairment, climate effects, or materials
effects alters key conclusions from the
2020 review. The PA also considers
quantitative analyses of visibility
impairment and the extent to which
they may indicate different conclusions
from those in the 2020 review regarding
the degree of protection from adverse
effects provided by the current
secondary standards.
Consistent with the approaches used
in previous reviews, the quantitative
analyses in the PA utilized a two-phase
assessment for visibility impairment.
First, the PA considered the
appropriateness of the elements
(indicator, averaging time, form, and
level) of the visibility index for
providing protection against PM-related
visibility effects. Second, the PA
evaluated the relationship between the
current secondary 24-hour PM2.5
standard and the visibility index.
With regard to the appropriateness of
the visibility index and its target level
of protection against PM-related
visibility effects, the PA notes that there
is limited information available in this
reconsideration beyond that available in
previous reviews to inform conclusions
on the elements (indicator, averaging
time, form, and level) of the visibility
index (described in more detail in
section V.C.1.a above). In considering
the available information, the PA
concludes that the available information
continues to support a visibility index
with estimated light extinction as the
indicator, a 24-hour averaging time, and
a 90th percentile form, averaged over
three years, with a level within the
range of 20 to 30 dv.
With regard to the relationship
between the current secondary 24-hour
PM2.5 standard and the visibility index,
the PA presents updated analyses based
on recent air quality information, with
a focus on locations meeting the current
secondary 24-hour PM2.5 and PM10
standards. In the absence of advances in
the monitoring methods for directly
measuring light extinction, and given
the lack of a robust monitoring network
for the routine measurement of light
extinction across the U.S. (section
V.B.1.a), as in previous reviews, the PA
analyses use calculated light extinction
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to estimate PM-related visibility
impairment (U.S. EPA, 2022b, section
5.3.1.2). Compared to the 2012 review,
updated analyses incorporate several
refinements. These include (1) the
evaluation of three versions of the
IMPROVE equation to calculate light
extinction (U.S. EPA, 2022b, Appendix
D, Equations D–1 through D–3) in order
to better understand the influence of
variability in equation inputs; 142 (2) the
use of 24-hour relative humidity data,
rather than monthly average relative
humidity as was used in the 2012
review (U.S. EPA, 2022b, section
5.3.1.2, Appendix D); and (3) the
inclusion of the coarse fraction in the
estimation of light extinction (U.S. EPA,
2022b, section 5.3.1.2, Appendix D).
The PA’s updated analyses include 60
monitoring sites that measure PM2.5 and
PM10 that are geographically distributed
across the U.S. in both urban and rural
areas (U.S. EPA, 2022b, Appendix D,
Figure D–1).143
In areas that meet the current 24-hour
PM2.5 standard for the 2017–2019 time
period, all sites have light extinction
estimates at or below 26 dv using the
original and revised IMPROVE
equations (U.S. EPA, 2022b, section
5.3.1.2). In addition, the four locations
that exceeds the current 24-hour PM2.5
standard have light extinction estimates
that range from 22 to 27 dv when using
the original IMPROVE equation (U.S.
EPA, 2022b, Figure 5–3) and from 22 to
29 dv when using the revised IMPROVE
equation (U.S. EPA, 2022b, Figure 5–4).
The analyses presented in the PA
indicate similar findings to those from
the analyses in the 2012 and 2020
reviews, i.e., the updated quantitative
analysis shows that the 3-year visibility
metric was no higher than 30 dv (the
upper end of the range of target levels
of protection) at sites meeting the
current secondary PM standards, and at
most such sites the 3-year visibility
index values are much lower (e.g., an
average of 20 dv across the 60 sites).144
142 While the PM
2.5 monitoring network has an
increasing number of continuous FEM monitors
reporting hourly PM2.5 mass concentrations, there
continue to be data quality uncertainties associated
with providing hourly PM2.5 mass and component
measurements that could be input into IMPROVE
equation calculations for sub-daily visibility
impairment estimates. Therefore, the inputs to these
light extinction calculations are based on 24-hour
average measurements of PM2.5 mass and
components, rather than sub-daily information.
143 These sites are those that have a valid 24-hour
PM2.5 design value for the 2015–2017 period and
met strict criteria for PM species for this analysis,
based on 24-hour average PM2.5 and PM10–2.5 mass
and component data that were available from
monitors in the IMPROVE network, CSN, and
NCore Multipollutant Monitoring Network (U.S.
EPA, 2022b, Appendix D).
144 As noted above in section V.1.C.b, when light
extinction is calculated using the original IMPROVE
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When light extinction is calculated
using the updated IMPROVE equation
from Lowenthal and Kumar (2016), the
resulting 3-year visibility metrics are
slightly higher at all sites compared to
light extinction calculated using the
original and revised IMPROVE
equations (U.S. EPA, 2022b, Figure 5–5).
The slightly higher estimates of light
extinction are consistent with the higher
OC multiplier included in the IMPROVE
equation from Lowenthal and Kumar
(2016), reflecting the use of data from
remote areas with higher concentrations
of organic PM when validating that
equation. As such, it is important to
note that the Lowenthal and Kumar
(2016) version of the IMPROVE equation
may overestimate light extinction in
non-remote areas, including in the
urban areas included in the analyses
presented in the PA.
Nevertheless, when light extinction is
calculated using the Lowenthal and
Kumar (2016) equation for those sites
that meet the current 24-hour PM2.5
standard, the 3-year visibility metric is
generally at or below 28 dv.145 For the
sites that exceed the current 24-hour
PM2.5 standard, three of the sites have a
3-year visibility metric ranging between
26 dv and 30 dv, while one site in
Fresno, California that exceeds the
current 24-hour PM2.5 standard has a 3year visibility index value of 32 dv
(compared to 29 dv when light
extinction is calculated with the original
IMPROVE equation) (see U.S. EPA,
2022b, Appendix D, Table D–3). At this
site, it is likely that the 3-year visibility
metric using the Lowenthal and Kumar
(2016) equation would be below 30 dv
if PM2.5 concentrations were reduced
such that the 24-hour PM2.5 level of 35
mg/m3 was attained.
In the 2012 review, the EPA noted
that PM2.5 is the size fraction of PM
responsible for most of the visibility
impairment in urban areas (77 FR
38980, June 29, 2012). Data available at
the time of the 2012 review suggested
that PM10–2.5 is often a minor contributor
to visibility impairment (U.S. EPA,
equation, all 60 sites have 3-year visibility metrics
below 30 dv, 58 sites are at or below 25 dv, and
26 sites are at or below 20 dv (see U.S. EPA, 2022b,
Appendix D, Table D–3). When light extinction is
calculated using the revised IMPROVE equation, all
60 sites have 3-year visibility metrics below 30 dv,
56 sites are at or below 25 dv, and 26 sites are at
or below 20 dv (see U.S. EPA, 2022b, Appendix D,
Table D–3).
145 As noted above in section V.1.C.b, when light
extinction is calculated using the Lowenthal and
Kumar IMPROVE equation, 59 sites have 3-year
visibility metrics below 30 dv, 45 sites are at or
below 25 dv, and 15 sites are at or below 20 dv.
The one site with a 3-year visibility metric of 32 dv
exceeds the secondary 24-hour PM2.5 standard, with
a design value of 56 mg/m3 (see U.S. EPA, 2022b,
Appendix D, Table D–3).
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2010a), though it may make a larger
contribution in some areas in the desert
southwestern region of the U.S.
However, at the time of the 2012 review,
there were few data available from
PM10–2.5 monitors to quantify the
contribution of coarse PM to calculated
light extinction. Since that time, an
expansion in PM10–2.5 monitoring efforts
has increased the availability of data for
use in estimating light extinction with
both PM2.5 and PM10–2.5 concentrations
included as inputs in the equations. The
analysis in the 2020 review addressed
light extinction at 20 of the 67 PM2.5
sites where collocated PM10–2.5
monitoring data were available. Since
the 2020 review, PM10–2.5 monitoring
data are available at more locations and
the analyses presented in the PA
include those for light extinction
estimated with coarse and fine PM at all
60 sites. Generally, the contribution of
the coarse fraction to light extinction at
these sites is minimal, contributing less
than 1 dv to the 3-year visibility metric,
as assessed and presented in the 2020
PA (U.S. EPA, 2020a, section 5.2.1.2).
However, the PA notes that in the
updated quantitative analyses, only a
few sites were in locations that would
be expected to have high concentrations
of coarse PM, such as the Southwest.
These results are consistent with those
in the analyses in the 2019 ISA, which
found that mass scattering from PM10–2.5
was relatively small (less than 10%) in
the eastern and northwestern U.S.,
whereas mass scattering was much
larger in the Southwest (more than 20%)
particularly in southern Arizona and
New Mexico (U.S. EPA, 2019a, section
13.2.4.1, p. 13–36).
In summary, the findings of these
updated quantitative analyses are
generally consistent with those in the
2012 and 2020 reviews. The 3-year
visibility metric was generally below 26
dv in most areas that meet the current
24-hour PM2.5 standard when light
extinction is calculated using the
original and revised IMPROVE
equations, and generally at or below 28
dv when using the Lowenthal and
Kumar (2016) equation to estimate light
extinction. Small differences in the 3year visibility metric were observed
between the variations of the IMPROVE
equation. When light extinction is
calculated using the revised IMPROVE
equation, there is a generally ±1–2 dv at
the study locations compared to light
extinction calculated using the original
IMPROVE equation (U.S. EPA, 2022b,
Appendix D, Table D–3). When light
extinction is calculated using the
Lowenthal and Kumar (2016) equation,
the difference compared to using either
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the original or revised IMPROVE
equation generally ranges from no
difference to up to 4 dv greater in areas
that meet the current secondary 24-hour
PM2.5 standard (U.S. EPA, 2022b,
Appendix D, Table D–3). As noted in
previous reviews, a change of 1 to 2 dv
in light extinction under many viewing
conditions will be perceived as a small,
but noticeable, change in the
appearance of a scene, regardless of the
initial amount of visibility impairment
(U.S. EPA, 2004a; U.S. EPA, 2010a).
Given that there is more variability
when estimating light extinction using
the Lowenthal and Kumar (2016)
IMPROVE equation compared to the
original or revised IMPROVE equations,
it is important to recognize that the PA
notes that the Lowenthal and Kumar
(2016) equation may not be appropriate
for all locations and source types. For
example, the larger multiplier used in
the Lowenthal and Kumar (2016) may
be more appropriate for estimating light
extinction in more remote areas where
there is more aged and oxygenated
organic PM compared to in urban areas.
As such, the PA recognizes that one
version of the IMPROVE equation is not
necessarily more accurate or precise in
estimating light extinction, and that
differences in locations may support the
selection of inputs to the IMPROVE
equation or of the appropriate IMPROVE
equation to estimate light extinction on
a regional basis rather than on a national
basis. Overall, regardless of the
IMPROVE equation that is used to
estimate light extinction, in areas that
meet the current 24-hour PM2.5
standards, the 3-year visibility metric is
at or below 28 dv, which is in the upper
range of levels for the target level of
protection identified from the public
preference studies (i.e., 20 to 30 dv). In
fact, even in areas that exceed the
secondary 24-hour PM2.5 standard, and
regardless of the IMPROVE equation
that is used to calculate light extinction,
all study locations have 3-year visibility
index values at or below 30 dv, which
is the upper end of the range of target
levels of protection.
With regard to PM-related climate
effects, the PA recognizes that while the
evidence base has expanded since the
completion of the 2009 ISA, the recent
evidence has not appreciably improved
the understanding of the spatial and
temporal heterogeneity of PM
components that contribute to climate
forcing (U.S. EPA, 2022b, sections
5.3.2.1.1 and 5.5). Despite continuing
research, there are still significant
limitations in quantifying the
contributions of PM and PM
components to the direct and indirect
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effects on climate forcing (e.g., changes
to the pattern of rainfall, changes to
wind patterns, effects on vertical mixing
in the atmosphere) (U.S. EPA, 2022b,
sections 5.3.2.1.1 and 5.5). In addition,
while a number of improvements and
refinements have been made to climate
models since the 2012 review, these
models continue to exhibit variability in
estimates of the PM-related climate
effects on regional scales (e.g., ∼100 km)
compared to simulations at the global
scale (U.S. EPA, 2022b, sections
5.3.2.1.1 and 5.5). While recent research
has added to the understanding of
climate forcing on a global scale, there
remain significant limitations to
quantifying potential adverse effects
from PM on climate in the U.S. and how
they would vary in response to
incremental changes in PM
concentrations in the U.S. Overall, the
PA recognizes that while new research
is available on climate forcing on a
global scale, the remaining uncertainties
and limitations are significant, and the
new global scale research does not
translate directly to use at regional
spatial scales. Thus, the evidence does
not provide a clear understanding at the
spatial scales needed for the NAAQS of
a quantitative relationship between
concentrations of PM mass in ambient
air and the associated climate-related
effects (U.S. EPA, 2022b, sections
5.3.2.2.1 and 5.5). The PA concludes
that the evidence does not call into
question the adequacy of the current
secondary PM standards for climate
effects.
With regard to materials effects, the
PA notes the availability of recent
evidence in this reconsideration related
to the soiling process and the types of
materials that are affected. Such
evidence provides some limited
information to inform dose-response
relationships and damage functions
associated with PM, though most recent
studies have been conducted outside the
U.S. in areas where PM concentrations
in ambient air are higher than those
observed in the U.S. (U.S. EPA, 2022b,
section 5.3.2.1.2; U.S. EPA, 2019a,
section 13.4). The recent evidence
includes studies examining PM-related
effects on the energy efficiency of solar
panels and passive cooling building
materials, though there remains
insufficient evidence to establish
quantitative relationships between PM
in ambient air and these or other
materials effects (U.S. EPA, 2022b,
section 5.3.2.1.2). While recent research
has expanded the body of evidence for
PM-related materials effects, the PA
recognizes the lack of information to
inform quantitative analyses assessing
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materials effects or the potential public
welfare implications of such effects
(U.S. EPA, 2022b, section 5.3.2.2.2).
Thus, the PA concludes that the
evidence does not call into question the
adequacy of the current secondary PM
standards for materials effects.
Overall, the PA recognizes that the
newly available welfare effects
evidence, critically assessed in the 2019
ISA as part of the full body of evidence,
and visibility effects evidence, assessed
in the ISA Supplement, reaffirms the
conclusions on the visibility, climate,
and materials effects of PM as
recognized in the 2012 and 2020
reviews (U.S. EPA, 2022b, sections
5.3.1.1, 5.3.2.1, and 5.5). Further, there
is a general consistency of the currently
available evidence with the evidence
that was available in previous reviews,
including with regard to key aspects of
the decision to retain the standards in
the 2012 and 2020 reviews (U.S. EPA,
2022b, sections 5.3.1.1, 5.3.2.1, and 5.5).
The quantitative analyses for visibility
impairment for recent air quality
conditions indicate that estimated light
extinction in areas meeting the current
secondary 24-hour PM2.5 standards have
a 3-year visibility index at or below 30
dv (i.e., the upper end of the range of
target levels of protection identified in
the 2012 and 2020 reviews) and most
areas have 3-year visibility index values
at or below the midpoint of the range of
target levels of protection (i.e., 25 dv)
(U.S. EPA, 2022b, sections 5.3.1.2 and
5.5). Collectively, the PA finds that the
evidence and quantitative informationbased considerations support
consideration of retaining the current
secondary PM standards, without
revision (U.S. EPA, 2022b, section 5.5).
3. Administrator’s Proposed Decision on
the Current Secondary PM Standards
This section summarizes the
Administrator’s considerations and
conclusions related to the current
secondary PM2.5 and PM10 standards
and presents his proposed decision that
no change is required for those
standards at this time. The CAA
provisions require the Administrator to
establish secondary standards that, in
the judgment of the Administrator, are
requisite to protect public welfare from
known or anticipated adverse effects
associated with the presence of the
pollutant in the ambient air. In so doing,
the Administrator seeks to establish
standards that are neither more nor less
stringent than necessary for this
purpose. The Act does not require that
standards be set at a zero-risk level, but
rather at a level that reduces risk
sufficiently so as to protect the public
welfare from known or anticipated
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adverse effects. The final decision on
the adequacy of the current secondary
standards is a public welfare policy
judgment to be made by the
Administrator. The decision should
draw on the scientific information and
analyses about welfare effects, and
associated public welfare significance,
as well as judgments about how to
consider the range and magnitude of
uncertainties that are inherent in the
scientific evidence and analyses. This
approach is based on the recognition
that the available evidence generally
reflects a continuum that includes
ambient air exposures at which
scientists agree that effects are likely to
occur through lower levels at which the
likelihood and magnitude of responses
become increasingly uncertain. This
approach is consistent with the
requirements of the provisions of the
Clean Air Act related to the review of
NAAQS and with how the EPA and the
courts have historically interpreted the
Act.
Given these requirements, the
Administrator’s final decision in this
reconsideration will be a public welfare
policy judgment that draws upon the
scientific and technical information
examining PM-related visibility
impairment, climate effects and
materials effects, including how to
consider the range and magnitude of
uncertainties inherent in that
information. The Administrator
recognizes that his final decision will be
based on an interpretation of the
scientific evidence and technical
analyses that neither overstates nor
understates their strengths and
limitations, nor the appropriate
inferences to be drawn.
As an initial matter in considering the
secondary standards, the Administrator
notes the longstanding body of evidence
for PM-related visibility impairment. As
in previous reviews, this evidence
continues to demonstrate a causal
relationship between ambient PM and
effects on visibility (U.S. EPA, 2019a,
section 13.2). The Administrator
recognizes that visibility impairment
can have implications for people’s
enjoyment of daily activities and for
their overall sense of well-being.
Therefore, as in previous reviews, he
considers the degree to which the
current secondary standards protect
against PM-related visibility
impairment. In so doing, and consistent
with previous reviews, the
Administrator considers the protection
provided by the current secondary
standards against PM-related visibility
impairment in conjunction with the
Regional Haze Program as a means of
achieving appropriate levels of
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protection against PM-related visibility
impairment in urban, suburban, rural,
and Federal Class I areas across the
country. Programs implemented to meet
the secondary PM NAAQS, along with
the requirements of the Regional Haze
Program established for protecting
against visibility impairment in Class I
areas, would be expected to improve
visual air quality across all areas.
In addition, the Administrator notes
that the Regional Haze Program was
established by Congress specifically to
achieve ‘‘the prevention of any future,
and the remedying of existing,
impairment of visibility in mandatory
Class I areas, which impairment results
from man-made air pollution,’’ and that
Congress established a long-term
program to achieve that goal (CAA
section 169A). The Administrator finds
that in adopting section 169A, Congress
set a goal of eliminating anthropogenic
visibility impairment at Class I areas, as
well as a framework for achieving that
goal which extends well beyond the
planning process and timeframe for
attaining secondary NAAQS. Thus,
recognizing that the Regional Haze
Program will continue to contribute to
reductions in visibility impairment in
Class I areas, the Administrator
proposes to conclude that addressing
visibility impairment in Class I areas is
beyond the scope of the secondary PM
NAAQS and that setting the secondary
PM NAAQS at a level that would
remedy visibility impairment in Class I
areas would result in standards that are
more stringent than is requisite.
In further considering what standards
are requisite to protect against adverse
public welfare effects from visibility
impairment, the Administrator adopts
an approach consistent with the
approach used in previous reviews
(section V.A.1.b). That is, he first
identifies an appropriate target level of
protection in terms of a PM visibility
index that accounts for the factors that
influence the relationship between
particles in the ambient air and
visibility (i.e., size fraction, species
composition, and relative humidity). He
then considers air quality analyses
examining the relationship between this
PM visibility index and the current
secondary 24-hour PM2.5 standard in
locations meeting the current 24-hour
PM2.5 and PM10 standards (U.S. EPA,
2022b, section 5.3.1.2).
To identify a target level of protection,
the Administrator first considers the
characteristics of the visibility index
and defines its elements (indicator,
averaging time, form, and level). With
regard to the indicator for the visibility
index, the Administrator recognizes that
there is a lack of availability of methods
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and an established network for directly
measuring light extinction, consistent
with the conclusions reached in the PA
(U.S. EPA, 2022b, section 5.3.1.1) and
with the CASAC’s recommendation for
additional research on direct
measurement methods for light
extinction (Sheppard, 2022a, p. 21 of
consensus responses). He notes that in
the 2012 and 2020 reviews, given the
lack of such monitoring data, the EPA
used an index based on estimates of
light extinction by PM2.5 components
calculated using an adjusted version of
the original IMPROVE algorithm. As
described above (sections V.B.1.a and
V.D.2), this algorithm allows the
estimation of light extinction using
routinely monitored components of
PM2.5 and PM10–2.5,146 along with
estimates of relative humidity. While
revisions have been made to the
IMPROVE algorithm since the 2012
review (U.S. EPA, 2022b, section
5.3.1.1), the Administrator recognizes
that our fundamental understanding of
the relationship between ambient PM
and light extinction has changed little
since the 2012 review. He further
recognizes that the results of the
quantitative analyses in the PA that
examined three versions of the
IMPROVE equation indicate that there
are very small differences in estimates
of light extinction between the
equations, and that it is not always clear
that one version of the IMPROVE
equation is more appropriate for
estimating light extinction across the
U.S. than other versions of the
IMPROVE equation. He does, however,
recognize that the PA suggests that it
may be appropriate to select inputs to
the IMPROVE equation (e.g., the
multiplier for OC to OM) on a regional
basis rather than a national basis when
calculating light extinction (U.S. EPA,
2022b, section 5.3.1.2), and he further
notes the CASAC’s recognition that PMvisibility relationships are region
specific (Sheppard, 2022a, p. 21 of
consensus responses). In the absence of
a robust monitoring network to directly
measure light extinction (sections
V.B.1.a and V.D.2), he preliminarily
judges that estimated light extinction, as
calculated using one or more versions of
the IMPROVE algorithms, continues to
be the most appropriate indicator for the
visibility index in this reconsideration.
In further defining the characteristics
of a visibility index based on estimates
of light extinction, the Administrator
146 In
the 2012 review, the focus was on PM2.5
components given their prominent role in PMrelated visibility impairment in urban areas and the
limited data available for PM10–2.5 (77 FR 38980,
June 29, 2012; U.S. EPA, 2022b, section 5.3.1.2).
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considers the appropriate averaging
time, form, and level of the index. With
regard to the averaging time and form,
the Administrator notes that in previous
reviews, a 24-hour averaging time was
selected and the form was defined as the
3-year average of annual 90th percentile
values. The Administrator recognizes
that the evidence available in this
reconsideration and described in the PA
continue to provide support for the
short-term nature of PM-related
visibility effects. In so doing, he relies
on analyses of 24-hour and sub-daily
PM2.5 light extinction to inform his
conclusions on averaging time. The
Administrator notes that there are strong
correlations between 24-hour and subdaily (i.e., 4-hour average) PM2.5 light
extinction), indicating that a 24-hour
averaging time is an appropriate
surrogate for the sub-daily time periods
relevant for visual perception (U.S. EPA,
2011, Appendix G, section G.4). He
further recognizes that the longer
averaging time may be less influenced
by atypical conditions and/or atypical
instrument performance. Considering
this information, and noting that the
CASAC did not provide advice or
recommendations with regard to the
averaging time of the visibility index,
the Administrator preliminarily judges
that it the 24-hour averaging time
continues to be appropriate for the
visibility index.
With regard to the form of the
visibility index, the Administrator notes
that consistent with the approach taken
in other NAAQS, including the current
secondary 24-hour PM2.5 NAAQS, a
multi-year percentile form offers greater
stability to the air quality management
process by reducing the possibility that
statistically unusual indicator values
will lead to transient violations of the
standard. Using a 3-year average
provides stability from the occasional
effects of inter-annual meteorological
variability that can result in unusually
high pollution levels for a particular
year (U.S. EPA, 2011, p. 4–58). In
considering the percentile that would be
appropriate with the 3-year average, the
Administrator first notes that the
Regional Haze Program targets the 20%
most impaired days for improvements
in visual air quality in Class I areas.147
Based on analyses examining 90th, 95th,
and 98th percentile forms, the
Administrator preliminarily judges that
a focus similar to the Regional Haze
Program focused on improving the 20%
147 As noted above, the Administrator views the
Regional Haze Program as a complement to the
secondary PM NAAQS, and thus takes into
consideration its approach to improving visibility
in considering how to address visibility outside of
Class I areas.
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most impaired days suggest that the
90th percentile, which represents the
median of the 20% most impaired days,
such that 90% of days have visual air
quality that is at or below the target
level of protection of the visibility
index, would be reasonably expected to
lead to improvements in visual air
quality for the 20% most impaired days
(U.S. EPA, 2011, p. 4–59). In the
analyses of percentiles, the results
suggest that a higher percentile value
could have the effect of limiting the
occurrence of days with peak PMrelated light extinction in areas outside
of Federal Class I areas to a greater
degree. However, the Administrator
preliminarily concludes that it is
appropriate to balance concerns about
focusing on the group of most impaired
days with concerns about focusing on
the days with peak visibility
impairment. Additionally, the
Administrator notes that the CASAC did
not provide advice or recommendations
related to the form of the visibility
index. Therefore, the Administrator
preliminarily judges that it remains
appropriate to define a visibility index
in terms of a 24-hour averaging time and
a form based on the 3-year average of
annual 90th percentile values.
With regard to the level of the
visibility index, the Administrator first
notes that the information that is
available regarding the range of levels of
visibility impairment judged to be
acceptable by at least 50% of study
participants in the visibility preference
studies is largely the same as was in
previous reviews.148 As such, the
Administrator notes that the PA
identifies a range of 20 to 30 dv as
appropriate for considering the level for
the visibility index. Furthermore, the
Administrator notes that a level at the
upper end of the range (i.e., 30 dv) was
selected for the 2012 and 2020 reviews,
given the uncertainties and limitations
associated with the public preference
studies (U.S. EPA, 2022b, section
5.3.1.1). In considering the available
public preference studies and the range
of target levels of protection derived
from the studies, the Administrator
notes that, while methodologically
similar, the studies have inherent
differences that impact the responses
from the study participants. He notes
that the images used to evaluate public
preferences differed significantly
depending on geographical location,
and that public preferences for visual air
148 For reasons stated above, the Administrator
does not find it appropriate to use the most recent
preference study (Malm et al., 2019) for purposes
of identifying a target level of protection for the
visibility index.
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quality can vary depending on the
scenic elements depicted in the images.
He also recognizes that the older studies
(i.e., those in Denver, CO, and British
Columbia, Canada) used photographs,
paired with ambient measurements of
light extinction, as opposed to the
computer-generated images in more
recent studies (i.e., those in Phoenix,
AZ, and Washington, DC), which
introduces more variability in scene
appearance that can influence
preferences. Furthermore, the distances
of objects depicted in the images can
influence the perceived visibility
changes, as objects at a greater distance
have more sensitivity to changes in
visibility impairment compared to those
at shorter distances. The Administrator
recognizes that these differences, and
the uncertainties and limitations that
result from them, are important to
consider when identifying a target level
of protection for the visibility index,
particularly in identifying the
appropriate level of protection that
would be neither more nor less stringent
than necessary for a national standard.
In addition to the methodological
differences across the public preferences
studies, the Administrator takes note of
the uncertainties and limitations
associated with the studies and
discussed in the PA. In particular, the
Administrator notes that available
studies may not capture the full range
of visibility preferences in the U.S.
population, particularly given the
potential for preferences to vary based
on the visibility conditions commonly
encountered and the types of scenes
being viewed and factors that are not
captured by the methods used in
available preference studies may
influence people’s judgments on
acceptable visibility, including the
duration of visibility impairment, the
time of day during which light
extinction is greatest, and the frequency
of episodes of visibility impairment
(U.S. EPA, 2022b, section 5.3.1.1).
In considering the appropriate target
level of protection for the visibility
index, the Administrator also takes note
of the CASAC’s advice. Specifically, he
notes that the CASAC recognizes that
such a judgment is based on a limited
number of visibility preference studies,
with studies conducted in the western
U.S. reporting public preferences for
visibility impairment associated with
the lower end of the range of levels,
while studies conducted in the eastern
U.S. reporting public preferences
associated with the upper end of the
range. While the CASAC did not
specifically recommend a level for the
visibility index, they did state that a
visibility index of 30 deciviews ‘‘needs
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to be justified’’ (Sheppard, 2022a, p. 21
of consensus responses). In considering
the available information and the
CASAC’s advice, the Administrator
notes that the public preference studies
were conducted in several geographical
areas across the U.S., and while they
provide insight to regional preferences
for visibility impairment, none of these
studies identify a specific level of
visibility impairment that would be
perceived as ‘‘acceptable’’ or
‘‘unacceptable’’ across the whole U.S.
population. The Administrator notes
that there have long been significant
questions about how to set a national
standard for visibility that is not
overprotective for some areas of the U.S.
In establishing the Regional Haze
Program to improve visibility in Class I
areas, Congress noted that ‘‘as a matter
of equity, the national ambient air
quality standards cannot be revised to
adequately protect visibility in all areas
of the country.’’ H.R. Rep. 95–294 at
205. Similarly, in the 1997 review, the
Administrator at that time noted
significant differences in visibility in
the eastern U.S. compared to the
western U.S. due to background
conditions, found that a standard set to
protect against visibility impairment
nationwide would be significantly
overprotective and not justified for some
parts of the country, and concluded it
was appropriate to rely on the Regional
Haze Program in conjunction with the
secondary PM NAAQS to achieve the
requisite degree of protection from
visibility impairment (62 FR 38652, July
18, 1997). For the reasons noted above,
the Administrator is not seeking to set
a standard that would eliminate
visibility impairment in Class I areas,
but significant uncertainties remain
regarding how to judge visibility
impairment across the entire range of
daily outdoor activities for Americans
across the country. Thus, the
Administrator recognizes that there are
substantial uncertainties and limitations
in the public preference studies that
should be considered when selecting a
target level of protection for the
visibility index. The Administrator
proposes to conclude that the
uncertainties and variability inherent in
the public preference studies warrant
setting a higher target level of protection
than if the underlying methods and
results from the public preference
studies were more consistent. In so
doing, the Administrator first
preliminarily judges that, consistent
with similar judgments in past reviews,
it is appropriate to recognize that the
secondary 24-hour PM2.5 standard is
intended to address visibility
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impairment across a wide range of
regions and circumstances, and that the
current standard works in conjunction
with the Regional Haze Program to
improve visibility, and therefore, it is
appropriate to establish a target level of
protection based on the upper end of the
range of levels. In considering the
information available in this
reconsideration and the CASAC’s
advice, the Administrator proposes to
conclude that the protection provided
by a visibility index based on estimated
light extinction, a 24-hour averaging
time, and a 90th percentile form,
averaged over 3 years, set at a level of
30 dv (the upper end of the range of
levels) would be requisite to protect
public welfare with regard to visibility
impairment.
Having provisionally concluded that
it remains appropriate in this
reconsideration to define the target level
of protection in terms of a visibility
index based on estimated light
extinction as described above (i.e., with
a 24-hour averaging time; a 3-year, 90th
percentile form; and a level of 30 dv),
the Administrator next considers the
degree of protection from visibility
impairment afforded by the existing
secondary standards. He considers the
updated analyses of PM-related
visibility impairment presented in the
PA (U.S. EPA, 2022b, section 5.3.1.2),
which reflect several improvements
over the 2012 review. Specifically, the
updated analyses examine multiple
versions of the IMPROVE algorithm,
including the version incorporating
revisions since the 2012 review (section
V.B.1.a). This approach provides an
improved understanding of how
variation in equation inputs impacts
calculated light extinction (U.S. EPA,
2022b, Appendix D). In addition, all of
the sites included in the analyses had
PM10–2.5 data available, which allows for
better characterization of the influence
of the coarse fraction on light extinction
(U.S. EPA, 2022b, section 5.3.1.2).
The Administrator notes that the
results of these updated analyses are
consistent with the results from the
2012 and 2020 reviews. Regardless of
the IMPROVE equation used, these
analyses demonstrate that the 3-year
visibility metric is at or below 28 dv in
all areas meeting the current 24-hour
PM2.5 standard (section V.C.1.b). Given
the results of these analyses, the
Administrator concludes that the
updated scientific evidence and
technical information support the
adequacy of the current secondary PM2.5
and PM10 standards to protect against
PM-related visibility impairment. While
the inclusion of the coarse fraction had
a relatively modest impact on calculated
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light extinction in the analyses
presented in the PA, he nevertheless
recognizes the continued importance of
the PM10 standard given the potential
for larger impacts in locations with
higher coarse particle concentrations,
such as in the southwestern U.S., for
which only a few sites met the criteria
for inclusion in the analyses in the PA
(U.S. EPA, 2019a, section 13.2.4.1; U.S.
EPA, 2022b, section 5.3.1.2).
With regard to the adequacy of the
secondary 24-hour PM2.5 standard, the
Administrator notes that the CASAC
stated that ‘‘[i]f a value of 20–25
deciviews is deemed to be an
appropriate visibility target level of
protection, then a secondary 24-hour
PM2.5 standard in the range of 25–35 mg/
m3 should be considered’’ (Sheppard,
2022a, p. 21 of consensus responses).
The Administrator recognizes that the
CASAC recommended the
Administrator provide additional
justification for a visibility index target
of 30 dv but did not specifically
recommend that he choose an
alternative level for the visibility index.
The Administrator has considered the
CASAC’s advice, together with the
available scientific evidence and
quantitative information in reaching his
proposed conclusions. The
Administrator recognizes conclusions
regarding the appropriate weight to
place on the scientific and technical
information examining PM-related
visibility impairment including how to
consider the range and magnitude of
uncertainties inherent in that
information is a public welfare policy
judgment left to the Administrator. As
such, the Administrator notes his
conclusion on the appropriate visibility
index (i.e., with a 24-hour averaging
time; a 3-year, 90th percentile form; and
a level of 30 dv) and his conclusions
regarding the quantitative analyses of
the relationship between the visibility
index and the current secondary 24hour PM2.5 standard. In so doing, he
proposes to conclude that the current
secondary standards provide requisite
protection against PM-related visibility
effects. With respect to non-visibility
welfare effects, the Administrator
considers the evidence for PM-related
impacts on climate and on materials and
concludes that it is generally
appropriate to retain the existing
secondary standards and that it is not
appropriate to establish any distinct
secondary PM standards to address nonvisibility PM-related welfare effects.
With regard to climate, he recognizes
that a number of improvements and
refinements have been made to climate
models since the time of the 2012
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review. However, despite continuing
research and the strong evidence
supporting a causal relationship with
climate effects (U.S. EPA, 2019a, section
13.3.9), the Administrator notes that
there are still significant limitations in
quantifying the contributions of the
direct and indirect effects of PM and PM
components on climate forcing (U.S.
EPA, 2022b, sections 5.3.2.1.1 and 5.5).
He also recognizes that models continue
to exhibit considerable variability in
estimates of PM-related climate impacts
at regional scales (e.g., ∼100 km),
compared to simulations at the global
scale (U.S. EPA, 2022b, sections
5.3.2.1.1 and 5.5). The resulting
uncertainty leads the Administrator to
preliminarily conclude that the
scientific information available in this
reconsideration remains insufficient to
quantify, with confidence, the impacts
of ambient PM on climate in the U.S.
(U.S. EPA, 2022b, section 5.3.2.2.1) and
that there is insufficient information at
this time to base a national ambient
standard on climate impacts.
With respect to materials effects, the
Administrator notes that the available
evidence continues to support the
conclusion that there is a causal
relationship with PM deposition (U.S.
EPA, 2019a, section 13.4). He recognizes
that deposition of particles in the fine or
coarse fractions can result in physical
damage and/or impaired aesthetic
qualities. Particles can contribute to
materials damage by adding to the
effects of natural weathering processes
and by promoting the corrosion of
metals, the degradation of painted
surfaces, the deterioration of building
materials, and the weakening of material
components. While some recent
evidence on materials effects of PM is
available in the 2019 ISA, the
Administrator notes that this evidence
is primarily from studies conducted
outside of the U.S. in areas where PM
concentrations in ambient air are higher
than those observed in the U.S. (U.S.
EPA, 2019a, section 13.4). Given the
limited amount of information on the
quantitative relationships between PM
and materials effects in the U.S., and
uncertainties in the degree to which
those effects could be adverse to the
public welfare, the Administrator
preliminarily judges that the scientific
information available in this
reconsideration remains insufficient to
quantify, with confidence, the public
welfare impacts of ambient PM on
materials and that there is insufficient
information at this time to support a
distinct national ambient standard
based on materials impacts.
Taken together, the Administrator
proposes to conclude that the scientific
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and technical information for PMrelated visibility impairment, climate
impacts, and materials effects, with its
attendant uncertainties and limitations,
supports the current level of protection
provided by the secondary PM
standards as being requisite to protect
against known and anticipated adverse
effects on public welfare. For visibility
impairment, this proposed conclusion
reflects his consideration of the
evidence for PM-related light extinction,
together with his consideration of
updated analyses of the protection
provided by the current secondary PM2.5
and PM10 standards. For climate and
materials effects, this conclusion reflects
his preliminary judgment that, although
it remains important to maintain
secondary PM2.5 and PM10 standards to
provide some degree of control over
long- and short-term concentrations of
both fine and coarse particles, it is
generally appropriate not to change the
existing secondary standards and that it
is not appropriate to establish any
distinct secondary PM standards to
address PM-related climate and
materials effects at this time. As such,
the Administrator recognizes that
current suite of secondary standards
(i.e., the 24-hour PM2.5, 24-hour PM10,
and annual PM2.5 standards) together
provide such control for both fine and
coarse particles and long- and shortterm visibility and non-visibility (e.g.,
climate and materials) 149 effects related
to PM in ambient air. His proposed
conclusions on the secondary standards
are consistent with advice from the
CASAC, which noted substantial
uncertainties remain in the scientific
evidence for climate and materials
effects. Thus, based on his consideration
of the evidence and analyses for PMrelated welfare effects, as described
above, and his consideration of CASAC
advice on the secondary standards, the
Administrator proposes not to change
those standards (i.e., the current 24-hour
and annual PM2.5 standards, 24-hour
PM10 standard) at this time. The
Administrator solicits comments on this
proposed conclusion.
The Administrator additionally
recognizes that the available evidence
on visibility impairment generally
reflects a continuum and that the public
preference studies did not identify a
specific level of visibility impairment
that would be perceived as ‘‘acceptable’’
or ‘‘unacceptable’’ across the whole U.S.
population. However, he notes a
149 As noted earlier, other welfare effects of PM,
such as ecological effects, are being considered in
the separate, on-going review of the secondary
NAAQS for oxides of nitrogen, oxides of sulfur and
PM.
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judgment of a target level of protection,
below 30 dv and down to 25 dv, could
be supported if more weight was put on
the public preference study performed
in the Phoenix, AZ, study (BBC
Research & Consulting, 2003), which
yielded the best results of the four
public preference studies in terms of the
least noisy preference results and the
most representative selection of
participants. While the Administrator
notes that CASAC did not recommend
revising the level of the current 24-hour
PM2.5 standard, the Administrator
recognizes that, should an alternative
level be considered for the visibility
index, that the CASAC recommends
also considering revisions to the
secondary 24-hour PM2.5 standard
(Sheppard, 2022a, p. 21 of consensus
responses). Thus, the Administrator
solicits comment on the appropriateness
of a target level of protection for
visibility below 30 dv and down as low
as 25 dv, and of revising the level of the
current secondary 24-hour PM2.5
standard to a level as low as 25 mg/m3.
Any comments on such revisions
should include an explanation of the
basis for the commenters’ views.
E. Proposed Decisions on the Secondary
PM Standards
Taking the above considerations into
account, upon reconsidering the public
welfare protection provided by the
current secondary PM standards for the
known and anticipated adverse effects
within the scope of this reconsideration,
in light of the currently available
scientific evidence and quantitative
information, the Administrator proposes
not to change the current secondary PM
standards at this time. In the
Administrator’s preliminary judgment,
such a suite of secondary PM standards
and the rationale supporting not
revising the current standards are
reasonably judged to reflect the
appropriate consideration of the
strength of the available evidence and
other information and their associated
uncertainties and the advice of CASAC.
The Administrator recognizes that the
final suite of standards will reflect his
ultimate judgment in the final
rulemaking, and in the on-going review
of the secondary NAAQS for oxides of
nitrogen, oxides of sulfur, and PM, as to
the suite of secondary PM standards that
are requisite to protect the public
welfare from known or anticipated
adverse effects associated with the
pollutant’s presence in the ambient air.
The final judgment to be made by the
Administrator will appropriately
consider the requirement for standards
that are neither more nor less stringent
than necessary and will recognize that
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the CAA does not require that secondary
standards be set at a zero-risk level, but
rather at a level that reduces risk
sufficiently so as to protect the public
welfare from known or anticipated
adverse effects.
The Administrator also solicits
comment on whether it would be
appropriate to revise the current
secondary 24-hour PM2.5 standard, in
conjunction with considering a lower
target level of protection for the
visibility index below 30 dv, and as low
as 25 dv. The Administrator takes note
that, while the CASAC did not
recommend changes to the current level
of 35 mg/m3 for the secondary 24-hour
PM2.5 standard, they indicated that
alternative levels should be considered
if a lower target level of protection (i.e.,
lower than 30 dv) for the visibility index
was judged to be appropriate. Thus, the
Administrator additionally solicits
comment on the appropriateness of
revising the level of the current
secondary 24-hour PM2.5 standard to a
level as low as 25 mg/m3. Any comments
on such revisions should include an
explanation of the basis for the
commenters’ views.
Having reached the proposed decision
described here based on interpretation
of the welfare effects evidence for this
reconsideration, as assessed in the 2019
ISA and ISA Supplement, and the
quantitative analyses of visibility
impairment in the PA; the evaluation of
policy-relevant aspects of the evidence
and quantitative analyses in the PA; the
advice and recommendations from the
CASAC; public comments received to
date in this reconsideration; and the
public welfare policy judgments
described above, the Administrator
recognizes that other interpretations,
assessments and judgments might be
possible. Therefore, the Administrator
solicits comment on the array of issues
associated with reconsideration of the
secondary PM standards, including
public welfare and science policy
judgments inherent in his proposed
decision, as described above, and the
rationales upon which such views are
based.
VI. Interpretation of the NAAQS for PM
A. Proposed Amendments to Appendix
K: Interpretation of the NAAQS for
Particulate Matter
The EPA proposes to revise appendix
K to make the PM10 data handling
procedures for the 24-hour PM10
standards specified in 40 CFR 50.6 more
consistent with those for other NAAQS
pollutants and to codify existing
practices. The proposed revisions,
which describe site-level computations,
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site-to-site combinations, and daily
validity requirements are discussed in
more detail below.
1. Updating Design Value Calculations
To Be on a Site-Level Basis
First, the EPA proposes to require
PM10 design values be calculated on a
site-level basis. Past practice has been to
calculate a monitor-level design value
for each individual PM10 monitor when
more than one monitor is located at a
single site; however, this practice is
inconsistent with the data handling for
PM2.5 and several other NAAQS
pollutants. This inconsistency with
PM2.5 has led to public confusion about
the applicable PM10 design value and
data completeness criteria at a site
because operators are more accustomed
to site-level monitoring requirements.
To resolve this confusion, the EPA
believes it would be appropriate to
identify a single design value for each
site; the EPA is proposing an analytic
approach to combine data collected
from multiple PM10 monitors collocated
at a site to obtain a single set of daily
PM10 concentration data for that site.
This proposal to move from monitorlevel to site-level PM10 design values is
supported by the high level of
consistency in the measurement data
obtained across the various Federal
reference and equivalent PM10
monitoring instruments currently in
operation (U.S. EPA, 2009a, section
3.4.1.1).
The proposed approach would
provide for monitoring agencies to
designate in their annual network plan
one monitor as the primary monitor for
each site.150 Once a primary monitor
has been determined for a site, missing
daily PM10 concentrations for the
primary monitor would be substituted
from any other monitors located at the
site. In the event of two or more
monitors operating at the same site,
missing daily PM10 concentrations for
the primary monitor would be
substituted with daily values averaged
across the other collocated monitors.
The EPA notes that at the time of this
proposal, there were more than 100 sites
nationwide with two or more monitors
operating simultaneously.
This proposed approach for
combining data across collocated
monitors at a site is consistent with the
existing approach described in
appendix N to part 50 for the current
PM2.5 NAAQS. The EPA invites public
comment on the scientific validity of
150 In the absence of a primary monitor
designation, the primary monitor would default to
the monitor with the most complete daily dataset
in each year.
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combining data across PM10 monitors
and the merits of the proposed approach
for combining data across multiple PM10
monitors collocated at a site.
2. Codifying Site Combinations To
Maintain a Continuous Data Record
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Second, and complementary to the
first proposed revision described above,
the EPA proposes to maintain the
existing practice of combining data from
nearby monitoring sites to determine a
valid design value, known as a ‘‘site
combination.’’ Site combinations
typically involve situations where one
site closes and another begins
monitoring a short distance away within
a few days, and the monitoring agency
wishes to combine the data from the two
sites to maintain a continuous data
record. The EPA Regional offices have
approved over ten site combinations for
PM10 since the promulgation of the 1987
PM10 NAAQS; these will be considered
approved site combinations if these
revisions are promulgated.
Relatedly, the EPA proposes to
maintain the existing practice of
allowing monitoring agencies to submit
site combination requests to the
appropriate Regional Administrator
through the EPA’s Air Quality System
(AQS) database. Site combinations may
be approved by the Regional
Administrator after they determine that
the measured air quality concentrations
do not differ substantially between the
two sites. To make this determination
for a requested site combination, the
Regional Administrator may request
additional information from the Agency
including detailed information on the
locations and distance between the two
sites, levels of ambient concentrations
measured at the two sites, and local
emissions or meteorology data. To
improve transparency, the EPA will
make records of all approved site
combinations available in the AQS
database and will update design value
calculations in AQS when approved site
combinations are implemented. The
EPA invites public comment on the
merits of the proposed process for
approving site combinations to obtain
valid design values for the PM10
NAAQS.
3. Clarifying Daily Validity
Requirements for Continuous Monitors
Third, the EPA proposes to maintain
the existing practice of considering
daily averages to be valid if at least 75
percent of the hourly averages (i.e., 18
hourly values) for the 24-hour period
are available unless a substitution test
can show validity on days with seven or
more missing hours.
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B. Proposed Amendments to Appendix
N: Interpretation of the NAAQS for
PM2.5
The EPA proposes to revise appendix
N by updating references to the
proposed revision(s) of the standards
and changing data handling provisions
related to combining data from nearby
monitoring sites to codify existing
practices that are currently being
implemented as EPA standard operating
procedures.
1. Updating References to the Proposed
Revision(s) of the Standards
The EPA proposes to maintain the
existing practice of combining data from
nearby monitoring sites to determine a
valid design value, known as a ‘‘site
combination.’’ Site combinations
typically involve situations where one
site closes and another begins
monitoring a short distance away within
a few days, and the monitoring agency
wishes to combine the data from the two
sites to maintain a continuous data
record. The EPA Regional offices have
approved over 40 site combinations for
PM2.5 since the promulgation of the
1997 PM2.5 NAAQS; these will be
considered approved site combinations
if these revisions are promulgated.
2. Codifying Site Combinations To
Maintain a Continuous Data Record
Relatedly, the EPA proposes to
maintain the existing practice of
allowing monitoring agencies to submit
site combination requests to the
appropriate Regional Administrator
through the EPA’s Air Quality System
(AQS) database. Site combinations may
be approved by the Regional
Administrator after they determine that
the measured air quality concentrations
do not differ substantially between the
two sites. To make this determination
for a requested site combination, the
Regional Administrator may request
additional information from the Agency
including detailed information on the
locations and distance between the two
sites, levels of ambient concentrations
measured at the two sites, and local
emissions or meteorology data. To
improve transparency, the EPA will
make records of all approved site
combinations available in the AQS
database and will update design value
calculations in AQS when approved site
combinations are implemented. The
EPA invites public comment on the
merits of the proposed process for
approving site combinations to obtain
valid design values for the PM2.5
NAAQS.
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VII. Proposed Amendments to Ambient
Monitoring and Quality Assurance
Requirements
The EPA is proposing revisions to
ambient air monitoring requirements for
PM to improve the usefulness of and
appropriateness of data used in
regulatory decision making. These
proposed changes focus on ambient
monitoring requirements found in 40
CFR parts 50 (appendix L), 53, and 58
with associated appendices (A, B, C, D,
and E). These proposed changes include
addressing updates in the approval of
reference and equivalent methods,
updates in quality assurance statistical
calculations to account for lower
concentration measurements, updates to
support improvements in PM methods,
a revision to the PM2.5 network design
to account for at-risk populations, and
updates to the Probe and Monitoring
Path Siting Criteria for NAAQS
pollutants.
The EPA last completed revisions to
PM ambient air monitoring regulations
as a part of the PM NAAQS review
completed in 2012 (78 FR 3085, January
15, 2013). This final rulemaking
included revisions to ensure the suite of
standards for PM provide requisite
protection of public health and welfare
as well as corresponding revisions to the
data handling conventions for PM and
to the ambient air monitoring, reporting,
and network design requirements. Other
pollutant-specific monitoring updates
have occurred in conjunction with
revisions to the NAAQS. In such cases,
the monitoring revisions were typically
finalized as part of the final rulemaking
for the NAAQS.151 Specific proposed
changes are described below.
A. Proposed Amendment in 40 CFR Part
50 (Appendix L): Reference Method for
the Determination of Fine Particulate
Matter as PM2.5 in the Atmosphere—
Addition of the Tisch Cyclone as an
Approved Second Stage Separator
The EPA is proposing a technical
change to appendix L to include the
addition of an alternative PM2.5 particle
size separator to that of the WINS and
the VSCC size separators. The new
separator is the TE–PM2.5C cyclone
manufactured by Tisch Environmental
Inc., Cleves, Ohio, and has been shown
to have performance equivalent to that
of the originally specified WINS
impactor with regards to aerodynamic
cutpoint and PM2.5 concentration
measurement. In addition, the new TE–
PM2.5C has a service interval
comparable to the VSCC separator and
is significantly longer than the service
151 Links to the NAAQS final rules are available
at: https://www.epa.gov/criteria-air-pollutants.
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interval for the WINS. Generally, the
TE–PM2.5C is also physically
interchangeable with the WINS and
VSCC where both are manufactured for
the same sampler. The proposal would
allow the WINS, VSCC, or TE–PM2.5C to
be used in a PM2.5 FRM sampler. As is
the case for the WINS and VSCC, the
TE–PM2.5C is now also an approved size
separator for candidate PM2.5 FEMs.
Currently, the EPA has designated one
PM2.5 sampler configured with TE–
PM2.5C separator as a Class II PM2.5
equivalent method and one as a PM10–2.5
equivalent method. Upon promulgation
of this proposed change to appendix L,
these instruments would be
redesignated as PM2.5 and PM10–2.5
FRMs, respectively. Owners of such
samplers would contact the sampler
manufacturer to receive a new reference
method label for the samplers.
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B. Proposed Amendments to Ambient
Air Monitoring Reference and
Equivalent Methods in 40 CFR Part 53
The EPA is proposing clarifications to
the regulations associated with
submittal of candidate FRM and FEM
applications for review by the EPA.
Revisions are also proposed in instances
where current regulatory specifications
are no longer pertinent and require
updating. In addition, the EPA has
compiled a list of noted minor errors to
correct in regulations associated with
the testing requirements and acceptance
criteria for Federal reference methods
(FRMs) and Federal equivalent methods
(FEMs) in part 53. These errors are
typically not associated with the content
of Federal Register documents but often
relate to transcription errors and
typographical errors in the electronic
CFR (eCFR) and printed versions of the
CFR.
1. Update to Program Title and Delivery
Address for FRM and FEM Application
and Modification Requests
The EPA is proposing to update the
name of the program and delivery
address for the EPA review of FRM and
FEM Applications and Modification
Requests (§ 53.4). These revisions are
due solely to organizational changes and
do not affect the structure or role of the
Reference and Equivalent Methods
Designation Program in reviewing new
FRM and FEM application requests and
requests to modify existing designated
instruments.
2. Requests for Delivery of a Candidate
FRM or FEM Instrument
As part of the current applicant
review process, § 53.4(d) allows the EPA
to request only candidate PM2.5 FRMs
and Class II or Class III equivalent
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methods for test purposes. The EPA
proposes to revise this section to allow
the EPA to request any candidate FRM,
FEM, or a designated FRM or FEM
associated with a Modification Request,
regardless of NAAQS pollutant type or
metric.
VOAG. Therefore, the EPA proposes to
add a commercially available
monodisperse aerosol generator—the
Model 1520 Flow-Focusing
Monodisperse Aerosol Generator, MSP
Corporation, Shoreview, MN—to the list
of approved generators for this purpose.
3. Amendments to Requirements for
Submission of Materials in § 53.4(b)(7)
for Language and Format
The EPA proposes to amend
§ 53.4(b)(7), which specifies the
format(s) in which all submissions must
be received, to specify that all written
application materials must be submitted
to the EPA in English in MS Word
format and that submitted data must be
submitted in MS Excel format.
7. Corrections to 40 CFR Part 53
(Reference and Equivalent Methods)
Certain provisions of § 53.14,
Modification of a reference or
equivalent method, incorrectly state an
EPA response deadline of 30 days for
receipt of modification materials in
response to an EPA notice. Per a 2015
amendment (80 FR 65460, 65416;
October 26, 2015), all EPA response
deadlines for modifications of reference
or equivalent methods are 90 days from
day of receipt.
The EPA proposes corrections to the
following tables: Table A–1 to Subpart
A of Part 53—Summary of Applicable
Requirements for Reference and
Equivalent Methods for Air Monitoring
of Criteria Pollutants identifies the
applicable 40 CFR part 50 appendices
and 40 CFR part 53 subparts for each
criteria pollutant. The four rows in the
section for PM10–2.5 erroneously do not
include the footnote instruction that the
aforementioned pollutant alternative
Class III requirements may be
substituted in regard to Appendix O to
Part 50—Reference Method for the
Determination of Coarse Particulate
Matter as PM10–2.5 in the Atmosphere.
Table B–1 SO2 states the interference
equivalent for each interferent is ±0.005
ppm for both the standard- and lowerrange limits, with the exception of nitric
oxide (NO) for the lower-range limit per
note 4. When testing the lower range of
SO2, the limit for NO is ±0.003 ppm,
therefore an incorrect lower limit
(±0.0003) is currently stated in note 4
for this exception to the SO2 lowerrange limit.
The EPA proposes corrections to the
following figures: After the EPA
received an inquiry regarding the
interaction of NO and O3, the EPA
investigated the interferent testing
requirements stated by 40 CFR part 53,
subpart B. The EPA has determined that
during the 2011 SO2 amendment and
subsequent 2015 O3 amendment, several
typographical errors were introduced
into Table B–3, the most significant of
which is the omission of note 3, which
instructs the applicant to not mix the
pollutant with the interferent.
Additionally, appendix A to subpart B
of part 53 provides figures depicting
optional forms for reporting test results.
Figure B–3 lists an incorrect formula:
the lower detectible limit section is
missing the proper operator in the LDL
4. Amendment to Designation of
Reference and Equivalent Methods
The EPA proposes to clarify the terms
of new FRM and FEM methods
(§ 53.8(a)) to ensure that candidate
samplers and analyzers are not publicly
announced, marketed, or sold as FRMs
until the EPA’s approval has been
formally announced in the Federal
Register.
5. Amendment to One Test Field
Campaign Requirement for Class III
PM2.5 FEMs
Field comparability tests for
candidate Class III PM2.5 FEMs include
the requirement that a total of five field
campaigns must be conducted at four
separate sites: A, B, C, and D. The site
D specifications of § 53.35(b)(1)(ii)(D)
require that the site ‘‘. . . shall be in a
large city east of the Mississippi River,
having characteristically high sulfate
concentrations and high humidity
levels.’’ However, dramatic decreases in
ambient sulfate concentration make it
difficult for applicants to routinely meet
the high sulfate concentration
requirement. Therefore, the EPA
proposes to revise the site D
specifications to read ‘‘. . . shall be in
a large city east of the Mississippi River,
having characteristically high humidity
levels.’’
6. Amendment to Use of Monodisperse
Aerosol Generator
Wind tunnel evaluation of candidate
PM10 inlets and evaluation of candidate
PM2.5 fractionators under static
conditions requires the generation and
use of monodisperse calibration aerosols
of specified aerodynamic sizes. In the
current regulations (§ 53.61(g)), the TSI
Incorporated Vibrating Orifice Aerosol
Generator (VOAG) is the only approved
monodisperse generator for this
purpose. However, TSI Incorporated no
longer manufacturers nor supports the
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calculation formula and Figure B–5 lists
an incorrect calculation metric: there is
a typesetting error in the calculation of
the standard deviation. The EPA
proposes to correct the typesetting
errors.
The EPA proposes correcting
typesetting errors in several formulas
provided throughout § 53.43.
C. Proposed Changes to 40 CFR Part 58
(Ambient Air Quality Surveillance)
1. Quality Assurance Requirements for
Monitors Used in Evaluations for
National Ambient Air Quality Standards
The EPA has evaluated the quality
system as part of the PM NAAQS
reconsideration and identified several
areas that could be improved in light of
lower average ambient PM2.5
concentrations across the country and
the proposed more revised primary
annual PM2.5 NAAQS described in
section II above. Thus, we assessed
PM2.5 concentration data across a range
of values to determine if any changes
were warranted to their use in the
statistics used to evaluate the data
qualify in the PM2.5 network. This
section describes that work and any
proposed changes as a result. Other
changes proposed in this section
include clarifications and other
improvements that will better assist
with the consistency and operations of
quality assurance programs.
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a. Quality System Requirements
The EPA has reconsidered the
appendix A, section 2.3.1.1, goal for
acceptable measurement uncertainty for
automated and manual PM2.5 methods
currently stated as an upper 90 percent
confidence limit for the coefficient of
variation (CV) of 10 percent and ±10
percent for total bias. The average PM2.5
concentrations across the nation have
steadily declined since the
promulgation of the first PM2.5 standard
(U.S. EPA, 2022, section 2.3). As
ambient concentrations decrease, the
bias is inflated using the current bias
statistic in 4.2.5. The EPA has
developed a new bias statistic to
minimize the effect of low PM2.5
concentrations on bias and is proposing
to revise section 4.2.5 to implement this
new bias statistic. The EPA has
concluded that with this change to the
bias statistic, the coefficient of variation
(CV) of 10 percent and ±10 percent for
total bias is still an acceptable goal for
estimating total bias in the networks.
The technical justification and
background for this change is
documented in a technical
memorandum to the docket for this
rulemaking titled ‘‘Task 16 on PEP/
VerDate Sep<11>2014
20:11 Jan 26, 2023
Jkt 259001
NPAP Task Order: Bias and Precision
DQOs for the PM2.5 Ambient Air
Monitoring Network.’’ 152
The EPA is proposing to update and
clarify ambient air monitoring
requirements found in appendix A,
section 2.6.1, pertaining to EPA Protocol
Gas standards used for ambient air
monitoring and the Ambient Air
Protocol Gas Verification Program.
Appendix A would be revised to clarify
that in order to participate in the
Ambient Air Protocol Gas Verification
Program, producers of Protocol Gases
must adhere to the requirements of 40
CFR 75.21(g), and only regulatory
ambient air monitoring programs may
submit cylinders for assay verification
to the EPA Ambient Air Protocol Gas
Verification Program. The EPA is
proposing to include an allowable
uncertainty of ±2.0 percent for EPA
Protocol Gas standards used in ambient
air monitoring. This allowable
uncertainty limit would match the
existing limit set by the EPA’s
continuous emission monitoring
program found in part 75, appendix A,
section 5.1.4(b), and would make the
EPA’s regulations of quality assurance
of ambient air monitors more uniform
and consistent.
b. Measurement Quality Check
Requirements
The EPA is proposing to remove
section 3.1.2.2 from appendix A. This
provision in the quality assurance
requirements for ambient air monitoring
allows for NO2 compressed gas
standards to be used to generate audit
standards. However, NO2 compressed
gas standards are not currently
designated by the EPA’s Office of
Research and Development (ORD) as an
EPA Protocol Gas Standard. As such,
this provision conflicts with section
2.6.1 of appendix A that requires that
any standard used for generating test
atmospheres be an EPA Protocol Gas
Standard. The EPA is aware that there
is a need for NO2 compressed gas
standards for direct read NO2
monitoring methods. If these NO2
compressed gas standards can, in the
future, be proven to be stable and
approvable as EPA Protocol Gas
Standards, the EPA will consider
restoring this provision to appendix A.
The EPA is proposing to revise the
requirement in section 3.1.3.3
152 Noah, G. (2022). Task 16 on PEP/NPAP Task
Order: Bias and Precision DQOs for the PM2.5
Ambient Air Monitoring Network. Memorandum to
the Rulemaking Docket for the Review of the
National Ambient Air Quality Standards for
Particulate Matter (EPA–HQ–OAR–2015–0072).
Available at: https://www.regulations.gov/docket/
EPA-HQ-OAR-2015-0072.
PO 00000
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Fmt 4701
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5665
pertaining to the validation of the
gaseous cylinders used for the National
Performance Audit Program (NPAP).
The EPA proposes to change the
requirement for annual verification to
the ORD-recommended certification
periods for standards identified in Table
2–3 of the EPA Traceability Protocol for
Assay and Certification of Gaseous
Calibration Standards (appendix A,
section 6.0(4)). These ORDrecommended periods are based on the
periods for which similar gas mixtures
over specific concentration ranges have
been shown to be stable, as documented
in the peer-reviewed literature or in
concentration stability data submitted
by the National Institute of Standards
and Technology (NIST) and specialty
gas producers and reviewed by the EPA.
In effect, this would decrease the cost
and burden on the Protocol Gas
Verification Program (PGVP), which
performs these verifications annually.
The EPA anticipates this will also
decrease the delay in returning tanks
back to the auditors. This would
provide auditors with longer periods
with valid certifications to perform
audits without annual interruptions for
the verification process.
The EPA is proposing to adjust the
minimum value required by appendix
A, section 3.2.4, to be considered valid
sample pairs for the PM2.5 Performance
Evaluation Program (PEP) from 3 mg/m3
to 2 mg/m3. As discussed above, ambient
PM2.5 concentrations have decreased,
and many samples being collected now
are below the 3 mg/m3 threshold and
deemed invalid for purposes of a valid
audit sample. Therefore, decreasing this
threshold from 3 mg/m3 to 2 mg/m3
would increase the number of valid PEP
sample pairs collected, which would
reduce the number of re-audits that
need to be performed to compensate for
invalid sample pairs. Inclusion of values
down to 2 mg/m3 would represent the
concentrations occurring in routine
monitoring operations and are included
in annual mean concentrations of the
networks. Reducing the number of reaudits would reduce audit costs to
monitoring organizations while better
representing the data in the networks.
The technical justification and
background for this change is
documented in a technical
memorandum to the docket for this
rulemaking titled ‘‘Task 16 on PEP/
NPAP Task Order: Bias and Precision
DQOs for the PM2.5 Ambient Air
Monitoring Network.’’ 153
153 Noah, G. (2022). Task 16 on PEP/NPAP Task
Order: Bias and Precision DQOs for the PM2.5
Ambient Air Monitoring Network. Memorandum to
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27JAP3
Federal Register / Vol. 88, No. 18 / Friday, January 27, 2023 / Proposed Rules
The EPA is proposing to update the
appendix A, section 4.2.1, Equations 6
and 7, for calculating the Collocated
Quality Control Sampler Precision
Estimate for PM10, PM2.5 and Pb.
The proposed changes are:
These new statistics are designed to
address the inflated precision values
that result from using these calculations
to compare low concentrations that are
now observed in the networks. The
current precision estimate uses a
relative percent difference (RPD) when
comparing two collocated samplers. As
the two numbers used in the
comparison get smaller, the statistic
generally produces a result that is
inflated. A precision statistic calculated
for low-concentration data may show
poor agreement even if the nominal
values are relatively close to each other.
By using the square root in the
denominator in these statistics, the
variability is more constant across all
concentrations thereby reducing the
inflated effect. The EPA believes this
proposed change would provide the
correct context for considering inflated
RPDs when calculating the bias
estimate. The technical justification and
background for this change is
documented in a technical
memorandum to the docket for this
rulemaking titled ‘‘Task 16 on PEP/
NPAP Task Order: Bias and Precision
DQOs for the PM2.5 Ambient Air
Monitoring Network.’’ 154
The EPA is proposing to update the
appendix A, section 4.2.5, Equation 8,
calculation for the Performance
Evaluation Programs Bias Estimate for
PM2.5 from
the Rulemaking Docket for the Review of the
National Ambient Air Quality Standards for
Particulate Matter (EPA–HQ–OAR–2015–0072).
Available at: https://www.regulations.gov/docket/
EPA-HQ-OAR-2015-0072.
154 Noah, G. (2022). Task 16 on PEP/NPAP Task
Order: Bias and Precision DQOs for the PM2.5
Ambient Air Monitoring Network. Memorandum to
the Rulemaking Docket for the Review of the
National Ambient Air Quality Standards for
Particulate Matter (EPA–HQ–OAR–2015–0072).
Available at: https://www.regulations.gov/docket/
EPA-HQ-OAR-2015-0072.
srobinson on DSKBC5CHB2PROD with PROPOSALS3
c. Calculations for Data Quality
Assessments
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C:\SHEILA\27JAP3.SGM
27JAP3
EP27JA23.003
5666
Federal Register / Vol. 88, No. 18 / Friday, January 27, 2023 / Proposed Rules
100 *
L~ d ·
z=l
n
z
where di
5667
meas - audit
audit
= - - - - - X 100
to
L~ s-1
z=l
n.JNAAQS concentration
Again, because the average ambient
PM concentrations across the nation
have steadily declined since the
promulgation of the PM2.5 standard, the
current method of calculation may not
be appropriate for determining bias for
these lower ambient concentrations and
newer sampling methodologies. The
current bias estimate uses a percent
difference (PD), referenced in appendix
A, section 4.1.1, when comparing an
audit sampler against a routine sampler.
As the two numbers used in the
comparison get smaller, the statistic
generally produces a result that is
inflated. A bias statistic calculated for
low-concentration data may show poor
agreement even if the nominal values
are relatively close to each other. This
may be misleading when trying to assess
bias and summarizing data to be used in
decision making. The EPA believes this
proposed change would provide the
correct context for considering inflated
RPDs when calculating the bias
estimate. The technical justification and
background for this change is
documented in a technical
memorandum to the docket for this
rulemaking titled ‘‘Task 16 on PEP/
NPAP Task Order: Bias and Precision
DQOs for the PM2.5 Ambient Air
Monitoring Network.’’ 155
khammond on DSKJM1Z7X2PROD with PROPOSALS3
155 Noah, G. (2022). Task 16 on PEP/NPAP Task
Order: Bias and Precision DQOs for the PM2.5
Ambient Air Monitoring Network. Memorandum to
the Rulemaking Docket for the Review of the
National Ambient Air Quality Standards for
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20:11 Jan 26, 2023
Jkt 259001
where si
meas - audit
= ------;===--- X 100
d. References
The EPA proposes to update the
references and hyperlinks in appendix
A, section 6. Several of the reference
documents have been updated and the
web locations have changed. This
proposal provides accuracy in
identifying and locating essential
supporting documentation so that
historical documents that do not
represent current practices are not used.
The EPA believes that it is important
that interested parties—especially
ambient air monitoring organizations
and stakeholders—have the most
current materials that provide
clarifications and guidance on the
interpretation of the regulations.
The EPA is also proposing to add a
footnote to Table A–1 of Appendix A to
Part 58—Minimum Data Assessment
Requirements for NAAQS Related
Criteria Pollutant Monitors. The
proposed footnote would clarify the
allowable time (i.e., every two weeks,
once a month, once a quarter, once
every 6 months, or distributed over all
4 quarters depending on the check)
between checks and encourage
monitoring organizations to perform
data assessments at regular intervals.
The EPA believes this proposal is
appropriate because the current
stipulation is unclear regarding the
specified interval for required
Particulate Matter (EPA–HQ–OAR–2015–0072).
Available at: https://www.regulations.gov/docket/
EPA-HQ-OAR-2015-0072.
PO 00000
Frm 00111
Fmt 4701
Sfmt 4702
✓audit
verifications. For example, under the
current flow rate verification for PM10
(low vol.), PM2.5, and Pb-PM10, a flow
check could be performed on April 1
and not checked again until May 31,
leaving approximately two months
between checks. Following this practice
would leave large intervals of time
between verifications, and if a check
fails using the described practice, an
unacceptably large data loss could
result. Also, a check could be performed
on the last day of a quality control (QC)
check interval and then on the first day
of the following interval, with only a
day or two between checks. This is not
the intended practice for QC measures
that are meant to ensure equipment is
continually operating properly over an
operational period. For this reason, the
EPA is proposing to clarify the
allowable time between checks.
2. Quality Assurance Requirements for
Prevention of Significant Deterioration
(PSD) Air Monitoring
This section on Quality Assurance
Requirements for Prevention of
Significant Deterioration (PSD) Air
Monitoring was developed in parallel to
the proposed changes associated with
appendix A. Thus, this section includes
similar detail and proposed changes for
evaluating quality system statistics for
PM2.5, clarifications, and other
improvements that will better assist
with the consistency and operations of
quality assurance programs for PSD.
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a. Quality System Requirements
The EPA has reconsidered the
appendix A, section 2.3.1.1, goal for
acceptable measurement uncertainty for
automated and manual PM2.5 methods
currently stated as an upper 90 percent
confidence limit for the CV of 10
percent and ±10 percent for total bias.
The average PM concentrations across
the nation have steadily declined since
the promulgation of the first PM2.5
standard (U.S. EPA, 2022, section 2.3).
As ambient concentrations decrease, the
bias is inflated using the current bias
statistic in section 4.2.5. Using a new
statistic to replace the existing statistic
in section 4.2.5 developed to eliminate
the effect of low concentrations on bias,
the EPA has concluded that the
coefficient of variation (CV) of 10
percent and ±10 percent for total bias is
still an acceptable goal for estimating
total bias in the networks. The technical
justification and background for this
change is documented in a technical
memorandum to the docket for this
rulemaking titled ‘‘Task 16 on PEP/
NPAP Task Order: Bias and Precision
DQOs for the PM2.5 Ambient Air
Monitoring Network.’’ 156
The EPA is proposing to update and
clarify ambient air monitoring
requirements found in appendix A,
section 2.6.1, pertaining to EPA Protocol
Gas standards used for ambient air
monitoring and the Ambient Air
Protocol Gas Verification Program.
Appendix A would be revised to clarify
that in order to participate in the
Ambient Air Protocol Gas Verification
Program, producers of Protocol Gases
must adhere to the requirements of 40
CFR 75.21(g), and only regulatory
ambient air monitoring programs may
submit cylinders for assay verification
to the EPA Ambient Air Protocol Gas
Verification Program. The EPA is
proposing to include an allowable
uncertainty of ±2.0 percent for EPA
khammond on DSKJM1Z7X2PROD with PROPOSALS3
156 Noah, G. (2022). Task 16 on PEP/NPAP Task
Order: Bias and Precision DQOs for the PM2.5
Ambient Air Monitoring Network. Memorandum to
the Rulemaking Docket for the Review of the
National Ambient Air Quality Standards for
Particulate Matter (EPA–HQ–OAR–2015–0072).
Available at: https://www.regulations.gov/docket/
EPA-HQ-OAR-2015-0072.
VerDate Sep<11>2014
20:11 Jan 26, 2023
Jkt 259001
Protocol Gas standards used in ambient
air monitoring. This allowable
uncertainty limit would match the
existing limit set by the EPA’s
continuous emission monitoring
program found in part 75, appendix A,
section 5.1.4(b), and would make the
EPA’s regulations more uniform and
consistent.
b. Measurement Quality Check
Requirements
The EPA is proposing to remove
section 3.1.2.2 from appendix A. This
provision in the quality assurance
requirements for ambient air monitoring
allows for NO2 compressed gas
standards to be used to generate audit
standards. However, NO2 compressed
gas standards are not currently
designated by the EPA’s ORD as an EPA
Protocol Gas Standard. As such, this
provision conflicts with section 2.6.1 of
appendix A that requires that any
standard used for generating test
atmospheres be an EPA Protocol Gas
Standard. The EPA is aware that there
is a need for NO2 compressed gas
standards for direct read NO2
monitoring methods. If these NO2
compressed gas standards can, in the
future, be proven to be stable and
approvable as EPA Protocol Gas
Standards, the EPA will consider
restoring this provision to appendix A.
The EPA is proposing to revise the
requirement in section 3.1.3.3
pertaining to the validation of the
gaseous cylinders used for the NPAP.
The EPA proposes to change the
requirement for annual verification to
the ORD-recommended certification
periods for standards identified in Table
2–3 of the EPA Traceability Protocol for
Assay and Certification of Gaseous
Calibration Standards (appendix A,
section 6.0(4)). These ORDrecommended periods are based on the
periods for which similar gas mixtures
over specific concentration ranges have
been shown to be stable, as documented
in the peer-reviewed literature or in
concentration stability data submitted
by NIST and specialty gas producers
and reviewed by the EPA. In effect, this
would decrease the cost and burden on
the PGVP, which performs these
PO 00000
Frm 00112
Fmt 4701
Sfmt 4702
verifications annually. The EPA
anticipates this will also decrease the
delay in returning tanks back to the
auditors. This would provide auditors
with longer periods with valid
certifications to perform audits without
annual interruptions for the verification
process.
The EPA is proposing to adjust the
minimum value required by appendix
A, section 3.2.4, to be considered valid
sample pairs for the PM2.5 Performance
Evaluation Program (PEP) from 3 mg/m3
to 2 mg/m3. As discussed above, ambient
PM2.5 concentrations have decreased,
and many samples being collected now
are below the 3 mg/m3 threshold and
deemed invalid for purposes of a valid
audit sample. Therefore, decreasing this
threshold from 3 mg/m3 to 2 mg/m3
would increase the number of valid PEP
sample pairs collected, which would
reduce the number of re-audits that
need to be performed to compensate for
invalid sample pairs. Inclusion of values
down to 2 mg/m3 would represent the
concentrations occurring in routine
monitoring operations and are included
in annual mean concentrations of the
networks. Reducing the number of reaudits would reduce audit costs to
monitoring organizations while better
representing the data in the networks.
The technical justification and
background for this change is
documented in a technical
memorandum to the docket for this
rulemaking titled ‘‘Task 16 on PEP/
NPAP Task Order: Bias and Precision
DQOs for the PM2.5 Ambient Air
Monitoring Network.’’ 157
c. Calculations for Data Quality
Assessments
The EPA is proposing to update the
appendix A, section 4.2.5, Equation 8,
calculation for the Performance
Evaluation Programs Bias Estimate for
PM2.5 from
157 Noah, G. (2022). Task 16 on PEP/NPAP Task
Order: Bias and Precision DQOs for the PM2.5
Ambient Air Monitoring Network. Memorandum to
the Rulemaking Docket for the Review of the
National Ambient Air Quality Standards for
Particulate Matter (EPA–HQ–OAR–2015–0072).
Available at: https://www.regulations.gov/docket/
EPA-HQ-OAR-2015-0072.
E:\FR\FM\27JAP3.SGM
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Federal Register / Vol. 88, No. 18 / Friday, January 27, 2023 / Proposed Rules
100 *
I~ d·
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n
z
where di
meas - audit
audit
=-----X
5669
100
to
L~
r=t
khammond on DSKJM1Z7X2PROD with PROPOSALS3
d. References
The EPA proposes to update the
references and hyperlinks in appendix
A, section 6. Several of the reference
documents have been updated and the
web locations have changed. This
proposal provides accuracy in
identifying and locating essential
supporting documentation so that
historical documents that do not
represent current practices are not used.
The EPA believes that it is important
that interested parties—especially
ambient air monitoring organizations
158 Noah, G. (2022). Task 16 on PEP/NPAP Task
Order: Bias and Precision DQOs for the PM2.5
Ambient Air Monitoring Network. Memorandum to
the Rulemaking Docket for the Review of the
National Ambient Air Quality Standards for
Particulate Matter (EPA–HQ–OAR–2015–0072).
Available at: https://www.regulations.gov/docket/
EPA-HQ-OAR-2015-0072.
20:11 Jan 26, 2023
1
n✓NAAQS concentration
Again, because the average ambient
PM concentrations across the nation
have steadily declined since the
promulgation of the PM2.5 standard, the
current method of calculation may not
be appropriate for determining bias for
these lower ambient concentrations and
newer sampling methodologies. The
current bias estimate uses a PD,
referenced in appendix A, section 4.1.1,
when comparing an audit sampler
against a routine sampler. As the two
numbers used in the comparison get
smaller, the statistic generally produces
a result that is inflated. A bias statistic
calculated for low-concentration data
may show poor agreement even if the
nominal values are relatively close to
each other. This may be misleading
when trying to assess bias and
summarizing data to be used in making
decisions. The EPA believes this
proposed change would provide the
correct context for considering inflated
RPDs when calculating the bias
estimate. The technical justification and
background for this change is
documented in a technical
memorandum to the docket for this
rulemaking titled ‘‘Task 16 on PEP/
NPAP Task Order: Bias and Precision
DQOs for the PM2.5 Ambient Air
Monitoring Network.’’ 158
VerDate Sep<11>2014
S·
Jkt 259001
where si
meas - audit
= ------;===--- X 100
and stakeholders—have the most
current materials that provide
clarifications and guidance on the
interpretation of the regulations.
The EPA is also proposing to add a
footnote to Table A–1 of Appendix A to
Part 58—Minimum Data Assessment
Requirements for NAAQS Related
Criteria Pollutant Monitors. The
proposed footnote would clarify the
allowable time (i.e., every two weeks,
once a month, once a quarter, once
every six months, or distributed over all
four quarters depending on the check)
between checks and encourage
monitoring organizations to perform
data assessments at regular intervals.
The EPA believes this proposal is
appropriate because the current
stipulation is unclear regarding the
specified interval for required
verifications. For example, under the
current flow rate verification for PM10
(low vol.), PM2.5, and Pb-PM10, a flow
check could be performed on April 1
and not checked again until May 31,
leaving approximately two months
between checks. Following this practice
would leave large intervals of time
between verifications, and if a check
fails using the described practice, an
unacceptably large data loss could
result. Also, a check could be performed
on the last day of a QC check interval
and then on the first day of the
following interval, with only a day or
two between checks. This is not the
intended practice for quality control
measures that are meant to ensure
equipment is continually operating
properly over an operational period. For
this reason, the EPA is proposing to
clarify the allowable time between
checks.
3. Proposed Amendments to PM
Ambient Air Quality Methodology
a. Proposal To Revoke Approved
Regional Methods (ARMs)
The EPA is proposing to remove
provisions for approval and use of
Approved Regional Methods (ARMs)
throughout parts 50 and 58 of the CFR.
ARMs are continuous PM2.5 methods
that have been approved specifically
PO 00000
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Sfmt 4702
✓audit
within a State or local air agency
monitoring network for purposes of
comparison to the NAAQS and to meet
other monitoring objectives. However, at
this time, there are no approved ARMs,
nor does the EPA anticipate any will be
requested. There are, however, more
than a dozen approved FEMs for PM2.5.
These approved FEMs are eligible for
comparison to the NAAQS and to meet
other monitoring objectives.
The EPA first proposed a process to
approve and use ARMs in January of
2006 (71 FR 2709, January 17, 2006). At
that time, there were no approved
continuous PM2.5 methods available to
compare to the NAAQS. The hope was
that approved ARMs would quickly
start the use of PM2.5 continuous
methods that worked well in monitoring
agency networks, since the benefits of
regulatory-grade automated methods
were not available at that time to air
agency programs. It was hoped that the
benefits of automated PM2.5 methods—
including real-time data reporting of
PM2.5 to support forecasting and
reporting of the AQI while also
providing a regulatory dataset eligible
for comparison to the PM2.5 NAAQS—
would encourage the development of
ARMs. The idea to encourage ARMs was
conceived following review of data
across the country demonstrating that
some agencies were achieving
acceptable data comparability with their
PM2.5 methods compared to collocated
FRMs; however, those methods did not
necessarily provide consistent data
across the country. At that time, there
were no approved PM2.5 continuous
FEMs and it was unclear how soon any
might be approved. However, by March
2008, the EPA’s Reference and
Equivalent Methods program had
approved the first PM2.5 continuous
FEM (73 FR 13224, March 12, 2008).
Over the next eight years, an additional
12 PM2.5 continuous FEMs were
approved. With many commercially
available PM2.5 continuous FEMs
available to air agencies, almost all
agencies soon began implementing one
or more PM2.5 FEMs in their network.
By 2020, monitoring agencies were
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khammond on DSKJM1Z7X2PROD with PROPOSALS3
reporting PM2.5 continuous FEM data
from 660 sites across the country (U.S.
EPA, 2022, section 2.2.3.1). Therefore,
with a large and growing network of
PM2.5 continuous FEMs and no
approved applications for ARMs in the
16 years that this provision has been
available, the EPA is proposing to
remove this provision, including any
related language, and to instead rely on
the existing network of approved PM2.5
FEMs and future approved FEMs. The
EPA notes that although references to
ARMs occur across part 50 and part 58,
the EPA is not reopening the substance
of the provisions where these references
occur and is only proposing regulatory
text for these provisions for the purpose
of removing the reference to ARMs.
b. Proposal for Calibration of PM
Federal Equivalent Methods (FEMs)
The EPA is proposing to modify its
specifications for PM FEMs described in
appendix C to part 58. Specifically, the
EPA is proposing that valid State, local,
and Tribal air monitoring data generated
in routine networks and submitted to
the EPA may be used to improve the PM
concentration measurement
performance of approved FEMs. This
approach, initiated by instrument
manufacturers, would be implemented
as a national solution in factory
calibrations of approved FEMs through
a firmware update. This would apply to
any PM FEM methods (i.e., PM10, PM2.5,
and PM10–2.5). The EPA is proposing this
modification because there are some
approved PM FEMs that are not
currently meeting measurement quality
objectives (MQOs) when evaluating data
nationally (U.S. EPA, 2022, section
2.2.3.1) meaning that an update to a
factory calibration may be appropriate;
however, there is not a clearly defined
process to update the calibration of an
FEM. While there are several types of
data available to use as the reference for
such updates (e.g., routinely operated
FRMs, audit program FRMs, and
chemical speciation sampler data), we
are proposing to use routinely operated
State, local, and Tribal FRMs as the
basis of comparison upon which to
calibrate FEMs. The goal of updating
factory calibrations would be to increase
the number of routinely operating FEMs
meeting MQOs across the networks in
which they are operated. The EPA has
received input from CASAC (Sheppard,
2022, p. 2 of consensus responses) and
State, local, and Tribal agencies
(National Association of Clean Air
Agencies (NACAA) Monitoring
Committee 01/20/22; Association of Air
Pollution Control Agencies (AAPCA)
Ambient Monitoring Committee 01/26/
2022; Tribal air quality professionals
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call on 02/17/22), all of which
expressed strong interest in improving
FEM data comparability to collocated
FRMs. While there are other approaches
that could improve data comparability
between PM FEMs and collocated
FRMs, The EPA believes that this
approach represents the most reliable
approach to update FEM factory
calibrations, since the existing FRM
network data that meets MQOs would
be used to set updated factory
calibrations. While the Agency is
proposing to add this language to more
expressly define a process to update
factory calibrations of approved PM
FEMs, the EPA believes that the existing
rules for updating approved FRMs and
FEMs found at 40 CFR 53.14 may also
continue to be utilized for this purpose
as appropriate. This section allows
instrument manufactures to submit to
the EPA a ‘‘Modification of a reference
or equivalent method.’’ Submitting a
modification request may be appropriate
to ensure an approved FEM continues to
meet the 40 CFR 53.9, ‘‘Conditions of
designation’’. Specifically, 40 CFR
53.9(c) requires that, ‘‘Any analyzer,
PM10 sampler, PM2.5 sampler, or
PM10–2.5 sampler offered for sale as part
of an FRM or FEM shall function within
the limits of the performance
specifications referred to in § 53.20(a),
§ 53.30(a), § 53.35, § 53.50, or § 53.60, as
applicable, for at least 1 year after
delivery and acceptance when
maintained and operated in accordance
with the manual referred to in
§ 53.4(b)(3).’’ Thus, instrument
manufactures are encouraged to seek
improvements to their approved FEM
methods as needed to continue to meet
data quality needs as operated across
the network. Instrument manufactures
have an option to pursue that now and
may have an additional option in the
future should we finalize this proposal
for calibration of PM FEMs.
In the PA (U.S. EPA, 2022b, section
2.2.3.1), the EPA analyzed the quality of
data from FRM samplers and
continuous PM2.5 FEM monitors
operating in routine networks to
determine whether they meet the MQOs
for PM2.5 FRMs and FEMs (40 CFR part
58, appendix A, section 2.3.1.1):
‘‘Measurement Uncertainty for
Automated and Manual PM2.5 Methods.
The goal for acceptable measurement
uncertainty is defined for precision as
an upper 90 percent confidence limit for
the coefficient of variation (CV) of 10
percent and ±10 percent for total bias.’’
When aggregating data across the
country, all PM2.5 FRMs meet the MQOs
for these methods. But of PM2.5
continuous FEMs aggregated across the
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country, some meet the MQOs, and
others do not.
One of the major challenges to
ensuring uniform data from PM
methods is that there are no accepted
standards against which to calibrate PM
methods. This was discussed in the
2004 Air Quality Criteria for Particulate
Matter (U.S. EPA, 2004b). PM reference
methods typically include the design
and performance requirements set forth
in the 40 CFR part 50. This is a contrast
to FRMs and FEMs for gaseous NAAQS
pollutants for which there are accepted
calibration standards; in the case of
ozone, there is even a standard reference
photometer that can be used to calibrate
approved methods in the field or
laboratory. For PM monitoring methods,
in the absence of accepted calibration
standards, acceptable data quality is
determined by comparing to other PM
FRMs. One challenge to comparing to
other PM FRMs during the initial field
testing for purposes of FEM approval is
that the dataset will in almost all cases
be substantially more limited than
what’s available in routine networks
once deployed. Thus, we seek to
encourage instrument manufacturers of
approved FEMs to evaluate data in
routine networks and consider
improvements to their FEM calibration,
as needed.
The EPA is proposing to use routine
and collocated FRM data operated by
State, local, and Tribal agencies as the
basis to update factory calibrations.
Routine State, local, and Tribal agency
FRM data form the largest portion of the
monitored air quality data used in
epidemiologic studies that are being
used to inform proposed decisions
regarding the adequacy of the public
health protection afforded by the
primary PM2.5 NAAQS, as discussed in
section II above. While the EPA is
proposing to use routine FRM data,
there are other reference datasets that
could be considered. For example, the
agency has an FRM audit program159
operated by independent operators and
laboratories. This program is highly
valuable to the success of the PM2.5
monitoring program by providing
independent data to assess the quality of
routinely operated FRMs and FEMs. If
we used the audit program data as the
basis for calibrating continuous
monitors, we would lose the ability to
collect independent data from audit
monitors to assess the operation of
routine monitors. Therefore, by using
routinely operated FRMs to calibrate
continuous FEMs, the Agency will
continue to maintain the independence
159 See: https://www.epa.gov/amtic/nationalpm25-performance-evaluation-program.
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of the FRM audit program to assess the
quality of routinely operated FRM and
continuous FEM data. The EPA also has
chemical speciation data available at
sites where the Chemical Speciation
Network (CSN) or IMPROVE samplers
are operated; however, these samplers
use technologies that operate at different
flow rates and with different-size
selective devices than approved FRMs,
and neither of these programs use FRMs
as the basis to collect samples.
Therefore, while CSN and IMPROVE
data can be useful to help determine the
aerosol chemistry of PM2.5 and may
provide additional validation of
collocated FRM or FEM data, by
themselves these data are not
appropriate to update factory calibration
of continuous FEMs.
The EPA proposes to direct
instrument companies and other
interested stakeholders to the EPA’s Air
Quality System (AQS) database 160 to
access the valid routine network data
that the Agency proposes to allow for
use in updating factory calibration of
continuous FEMs. There are several
ways to obtain data from the AQS
database, and many do not require
registration. For example, daily
processed datasets by year are publicly
available at the website of ‘‘PreGenerated Data Fields.’’ 161 The data
utilized would need to be valid PM
FRM and FEM data that are collocated
and aligned to the same date. For
example, for PM2.5 mass concentrations,
there are files by year for ‘‘ PM2.5 FRM/
FEM Mass’’ identified with a parameter
code of 88101. This information, already
aggregated to daily data, represent the
time-period of midnight-to-midnight
local standard time. While any years of
data may be considered, instrument
companies should normally use at least
two years of recent data where we are
past the certification period for the
previous-year data, which is May 1st of
each year. Including at least two years
of data is intended to address cases
where one of the years may have high
or low air quality concentrations. Data
in the current year and previous year
when we are not past the May 1st
certification date can be considered to
test data with a correction established
from a previous year or more than one
year. If multiple factors are included,
any new statistical correction or
corrections should be based on one or
more calendar years, with independent
testing of that data on another year or
160 See:
https://www.epa.gov/aqs.
https://aqs.epa.gov/aqsweb/airdata/
download_files.html.
161 See:
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more that was not used to develop the
equation(s).
The EPA also encourages instrument
companies to consider and implement
all the ways to optimize PM2.5 FEMs.
This may include, but is not limited to,
whether a method’s data can be
improved by operating the FEM inside
a heating, ventilation, and airconditioning (HVAC)-controlled shelter
or outside with minimal or no HVAC
control; optimizing heating of the
airstream to avoid condensation while
retaining semi-volatile PM captured on
the FRM; and any specialized guidance
or training that may help monitoring
agencies optimize their data quality and
comparability to collocated FRMs. Other
options might include updates to
unique coefficients used in the factory
calibration such as the density of the
aerosol, where applicable. Such changes
would normally need to be approved by
the EPA according to existing rules
found at 40 CFR 53.14.
Another challenge to consider is how
to deal with potential outliers that may
exist in the validated State, local, and
Tribal agency network data available
from AQS that would be used to
establish new factory calibrations. One
of the reasons to use data from the AQS
database is that there are tens of
thousands of collocated data pairs
available that include many of the
approved continuous PM2.5 FEMs.
Having a large data set will diminish the
effect of any one or more outliers.
However, acknowledging that the goal
of this proposed change is to update
factory calibrations to increase the
number of routinely operating FEMs
meeting MQOs across the networks in
which they are operated, we propose
that instrument companies may, but are
not required to, check for and exclude
any potential outliers. Additionally, we
propose that the range of data may be
limited to those concentrations that are
within the normal operating ranges of
most sites, but this is not required. This
approach, for example, could include
24-hour average PM2.5 concentrations
up to the level of the primary 24-hour
PM2.5 NAAQS or some percentile above
that level (e.g., 125% of the 24-hour
NAAQS). The rationale for this is that
there are very few sites with routine
concentrations above the level of the
primary 24-hour PM2.5 NAAQS, and the
establishment of any equation with this
data would need to be constructed
carefully to avoid having data below the
primary annual PM2.5 NAAQS drive the
coefficients used above the level of the
primary 24-hour PM2.5 NAAQS.
Ideally, the geographic coverage of the
data used in establishing a new factory
calibration would be national in scope;
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however, instrument companies can
only use the data that is available. For
widely used PM2.5 FEMs, this will not
be an issue, but for less-operated PM2.5
FEMs, there may be limitations in the
geographic scope of data produced.
Another challenge may be a large
grouping of sites in one part of the
country that drives development of an
equation used across all networks.
Instrument companies may limit the use
of sites with large groupings in one or
more geographical area so that the data
are more geographically representative
across the network so long as there is a
reasonable rationale as to why data from
certain sites are not being included.
With a new factory calibration available,
instrument companies will need to test
the performance of the updated
calibration across a variety of sites.
Testing of an updated factory calibration
can be accomplished by utilizing a
different year or years other than the
time-period used to establish the revised
factory calibration or a subset of data
across all years. Testing should also
include the range of sites in which the
method is used.
Building off the geographic location of
the sites in which an updated factory
calibration is tested with previously
collected data, the EPA considered what
performance level should be acceptable.
Ideally, an updated factory calibration
would work such that a significantly
larger number of, or all, individual sites
operating with the updated factory
calibration would meet the MQOs.
However, due to several complicating
factors such as seasonal changes in
temperature and humidity, elevation,
differences in aerosol composition, and
differences in concentration between
more polluted urban sites and relatively
cleaner rural sites (some of which read
well below the proposed revisions to the
level of the primary annual PM2.5
NAAQS discussed in section II above),
the EPA should not expect that every
site will necessarily meet the MQOs.
Therefore, the goal of this proposal is to
increase the number of routinely
operating FEMs meeting MQOs across
the networks in which they are
operated, especially for sites near the
level of the NAAQS proposed elsewhere
in this proposal. Since there are
multiple MQOs to consider, the EPA
proposes to place the most attention on
improvements to the bias MQO goal
because this statistic will likely have the
most influence on improving the
resultant data collected. In attempting to
address this goal, instrument companies
may be interested in testing their
original data used in field studies of
their candidate FEMs with an updated
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factory calibration. While this could be
a useful exercise to understand the
sensitivity of the original and any
updated factory calibration, the EPA
proposes not to require meeting the
performance criteria of the original field
testing as a condition of approving an
updated factory calibration.
Regarding how frequently factory
calibrations should be updated, the EPA
believes it would be most appropriate to
not define a specific time-period for
updates. Rather, updates should be
based on the available of quality data
being produced across the network.
Monitoring agencies routinely check
their data comparability to collocated
FRMs, including as part of annual data
certification where an AMP–256 report
describing data quality is included as
part of the certification package
(§ 58.15(c)). In addition, monitoring
agencies typically provide a more
thorough review of their networks and
accompanying data quality as part of the
five-year assessments due to the EPA
pursuant to 40 CFR 58.10(d).
Another important aspect to
implementing updated factory
calibrations is the treatment of data
already collected under the original
factory calibration. There are two time
periods to consider. First, there is the
time-period before the EPA approves an
updated to a factory calibration. We
propose that data collected prior to an
approved update to a factory calibration
be allowed to remain as measured based
on the factory calibration that was
approved at the time the data was
collected. Second, there is the timeperiod between when an updated
factory calibration is approved by the
EPA and when that updated calibration
is implemented in the field. While
ideally, this time-period would be short,
there may be reasons why some
agencies and the sites they run cannot
easily update the firmware with the
updated factory calibration. We solicit
comment on how to handle these
situations and whether there should be
an allowance to correct such data.
The EPA sought early input from
State, local, and Tribal monitoring
agencies (NACAA Monitoring
Committee 01/20/22; AAPCA Ambient
Monitoring Committee 01/26/2022;
Tribal air quality professionals call on
02/17/22) regarding how best to address
the issue of some PM2.5 FEMs having
bias issues. Many monitoring agencies
identified that they strongly favor a
national solution that can be
accomplished and implemented through
a firmware upgrade or similar resolution
that is consistent with the approach
described above. One State suggested
that the EPA should consider and allow
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site-by-site corrections between FRM
and collocated FEMs with ongoing
collocation at a 1:6 sample frequency for
FRMs. The rationale for site-by-site
corrections was that there are
differences in the types of aerosol
composition and concentration between
urban and rural locations and having
site-by-site corrections would ensure
that each type of location is individually
calibrated to a collocated FRM rather
than to a consistent factory calibration
that may average out any differences. In
contrast, other monitoring agencies
expressed concern about the challenges
of implementing a site-by-site approach,
especially for those agencies who stated
that they would not be able to redeploy
the FRMs that would be necessary to
perform the site-by-site corrections in
their networks for reasons including no
longer having FRMs, not having staff
available to support and operate the
FRMs, and no longer have gravimetric
laboratory capacity to support a larger
inventory of FRMs operating in their
networks.
The CASAC also provided input on
the FEM bias issue. As part of their
review of the draft PA, the CASAC
stated that ‘‘the FEM bias needs to be
addressed to make the FRMs and FEMs
more comparable’’ (Sheppard, 2022a, p.
2 of consensus responses). The CASAC
offered two options for the EPA to
consider. ‘‘One option would be to
allow states to develop correction
factors for co-located FRMs and FEMs.
These correction factors could be used
to adjust FEM concentrations downward
(or upward) to be comparable to FRMs.
Another option would be for the EPA to
revise the ‘equivalency box’ (EB) criteria
used to judge whether the bias of a new
continuous PM2.5 monitor relative to an
FRM is acceptable during field testing’’
(Sheppard, 2022a, p. 2 of consensus
responses). The CASAC’s first option is
consistent with the input received
during early input described above. The
EPA believes that the second option
should be considered in future reviews
of the PM NAAQS to help establish
updated goals for data quality from
PM2.5 FEMs. The existing network of
commercially available PM2.5 FRMs and
some of the continuous FEMs are
already meeting the MQOs at the
existing concentrations, which are at or
below the proposed revisions to the
level of the primary annual PM2.5
NAAQS discussed in section II above.
However, the EPA recognizes that not
all PM2.5 FEMs are meeting MQOs and,
therefore, the EPA intends to address
improvements to existing FEMs that are
not meeting MQOs as described above.
In attempting to address the
comparability of PM2.5 FEMs to
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collocated FRMs through our proposal
to allow updates to factory calibrations,
the EPA recognizes that other potential
solutions do not need to be mutually
exclusive. That is, there can be multiple
approaches to improve the
comparability of PM2.5 FRMs to
continuous FEMs. Therefore, the EPA
solicits comment on additional ways to
improve PM2.5 data comparability
between PM2.5 FRMs and collocated
continuous FEMs.
The EPA encourages early dialogue
with instrument companies considering
an update to any part (e.g., hardware,
software, and/or firmware revision) of
an approved FEM designation. Dialogue
with the EPA as well as applications by
instrument manufactures can be
initiated by contacting the EPA ORD’s
Reference and Equivalent (R&E)
Methods Designation program. The
contact information for this can be
found at 40 CFR 53.4, ‘‘Applications for
reference or equivalent method
determinations.’’
In summary, the EPA is proposing
that valid State, local, and Tribal air
monitoring data generated in routine
networks and submitted to the EPA may
be used to update factory calibrations
included as part of approved FEMs.
This approach, initiated by instrument
manufacturers, subject to EPA approval,
would be implemented as a national
solution in factory calibrations of
approved FEMs through a firmware
update. This would apply to any PM
FEM methods (i.e., PM10, PM2.5, and
PM10–2.5). As part of this process, the
EPA proposes that a range of data based
on the most representative
concentrations up to all available
concentrations may be used in
developing and testing a new factory
calibration, that a representative set of
geographic locations can be used, that
outliers may be included or not
included, that a new factory calibration
should be developed using data from at
least two years and tested on a separate
year(s) of data, that updates to factory
calibrations can occur as often as
needed, and should be evaluated by
monitoring agencies as part of routine
data assessments such as during
certification of data and five year
assessments, that the EPA recognizes
only data from existing operating sites is
available, and that an updated factory
calibration does not have to work with
the original field study data submitted
that led to the designation as an FEM.
The EPA solicits input on this approach
and any alternatives that would lead to
more sites meeting the bias MQO with
automated FEMs, especially for those
sites that are near the level of the
primary annual PM2.5 NAAQS, as
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4. Proposed Amendment to the PM2.5
Monitoring Network Design Criteria To
Address At-Risk Communities
To enhance protection of air quality
in communities subject to
disproportionate air pollution risk,
particularly in light of the proposed
range for a revised PM2.5 annual
standard, the EPA proposes to modify
our PM2.5 monitoring network design
criteria to include an environmental
justice factor that accounts for proximity
of populations at increased risk of
adverse health effects from PM2.5
exposures to sources of concern.
Specifically, the EPA proposes to
modify our existing requirement (40
CFR part 58, appendix D, section
4.7.1(b)(3)): ‘‘For areas with additional
required SLAMS, a monitoring station is
to be sited in an area of poor air
quality,’’ to additionally address at-risk
communities with a focus on
anticipated exposures from local
sources of emissions. The scientific
evidence evaluated in the 2019 ISA and
ISA Supplement indicates that subpopulations at potentially greater risk
from PM2.5 exposures include: children,
lower socioeconomic status (SES) 162
populations, minority populations
(particularly Black populations), and
people with certain preexisting diseases
(particularly cardiovascular disease and
asthma). The EPA is proposing that
communities with relatively higher
proportions of sub-populations at
greater risk from PM2.5 exposure within
the jurisdiction of a state or local
monitoring agency should be considered
‘‘at-risk communities’’ for these
purposes.
The PM2.5 network design criteria has
led to a robust national network of PM2.5
monitoring stations. These monitoring
stations are largely in Core-Based
Statistical Areas (CBSAs) 163 across the
country that include many PM2.5
monitor sites in at-risk communities.
Many of the epidemiologic studies
evaluated in the 2019 ISA and ISA
162 SES is a composite measure that includes
metrics such as income, occupation, and education,
and can play a role in populations’ access to
healthy environments and healthcare.
163 CBSAs—Metropolitan and Micropolitan
Statistical Areas are collectively referred to as CoreBased Statistical Areas. Metropolitan statistical
areas have at least one urbanized area of 50,000 or
more population, plus adjacent territory that has a
high degree of social and economic integration with
the core as measured by commuting ties.
Micropolitan statistical areas are a set of statistical
areas that have at least one urban cluster of at least
10,000 but less than 50,000 population, plus
adjacent territory that has a high degree of social
and economic integration with the core as measured
by commuting ties.
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Supplement, including those that
provide evidence of disparities in PM2.5
exposure and health risk in minority
populations and low SES populations,
often use data from these existing PM2.5
monitoring sites. However, we
anticipate that if the level of the annual
NAAQS is lowered, characterizing
localized air quality issues may become
even more important around local
emission sources. The EPA believes that
adding a network design requirement to
specifically locate monitors in at-risk
communities will improve our
characterization of exposures for at-risk
communities where localized air quality
issues may exist. Requiring the siting of
PM2.5 monitoring stations in at-risk
communities allows other methods to be
operated alongside PM2.5 measurements
to support multiple monitoring
objectives (40 CFR part 58, appendix D,
section 1.1). The EPA believes that it is
appropriate to formalize the monitoring
network’s characterization of PM2.5
concentrations in communities at
increased risk, to provide these areas
with the level of protection intended
with the PM2.5 NAAQS. The addition of
this requirement will also lead to
enhanced local data that will allow
regulatory air quality agencies to assist
communities to reduce exposures and to
help inform future implementation and
reviews of the NAAQS.
As described in section II.B.2 above
and in more detail in the PA (U.S. EPA,
2022b, section 3.3.2), the public health
implications of health effects associated
with PM2.5 in ambient air are dependent
on the type and severity of effects, as
well as the size of the population
affected and whether there are
populations and/or lifestages at
increased risk of a PM2.5-related health
effect. The 2019 ISA cites extensive
evidence indicating that ‘‘both the
general population as well as specific
populations and lifestages are at risk for
PM2.5-related health effects’’ (U.S. EPA,
2019, p. 12–1). Factors that may
contribute to increased risk of PM2.5related health effects include lifestage,
pre-existing diseases (cardiovascular
disease and respiratory disease), race/
ethnicity, and socioeconomic status.
The increased risk faced by these subpopulations raises environmental
justice 164 concerns. Section II of this
164 The EPA defines environmental justice as the
fair treatment and meaningful involvement of all
people regardless of race, color, national origin, or
income with respect to the development,
implementation, and enforcement of environmental
laws, regulations, and policies. The EPA further
defines the term fair treatment to mean that ‘‘no
group of people should bear a disproportionate
burden of environmental harms and risks, including
those resulting from the negative environmental
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preamble, section 12.5 of the 2019 ISA
(U.S. EPA, 2019a) and section 3.3.3 of
the ISA Supplement (U.S. EPA, 2022a)
provide extensive discussion on the
evidence for disparities in PM2.5
exposures and PM2.5-related health risks
of these sub-populations.
Consistent with the requirement of
the Clean Air Act to protect sensitive
sub-populations, the EPA is particularly
concerned with protecting subpopulations identified as being at higher
risk of adverse health effects from PM2.5
exposure in the 2019 ISA, ISA
Supplement and PA (U.S. EPA, 2019a;
U.S. EPA, 2022a; U.S. EPA, 2022b). The
EPA finds it appropriate to better
characterize the localized air quality in
communities with relatively higher
proportions of these sub-populations to
ensure these sub-populations receive
the intended level of protection of a
revised NAAQS proposed earlier in
section II. Thus, the EPA is proposing to
modify the PM2.5 ambient monitoring
network design criteria to add a
provision pertaining to sub-populations
identified as at increased risk for PM2.5
exposures and health risks associated
with PM2.5 (‘‘at-risk communities’’).
An enhanced network should include
representation of at-risk communities
who live near emission sources of
concern such as, but not limited to,
major ports, rail yards, airports,
industrial areas, or major transportation
corridors. The EPA finds it appropriate,
in light of the evidence of increased risk
to these communities, to better
characterize exposures given proximity
to local sources of concern. For
example, the EPA believes it is
worthwhile to characterize localized
ambient concentrations occurring when
there are emission sources located in a
part of a metropolitan area that are
different than the design value 165 site of
the same metropolitan area. Thus, while
there may be sites with higher overall
maximum concentrations in another
part of the same metropolitan area,
those sites are covered by our longstanding existing requirement that
monitors be placed ‘‘. . . in the area of
expected maximum concentration’’
[§ 58.1 and appendix D, section
4.7.1(b)(1)].
PM2.5 concentrations have generally
trended down when averaged across all
monitoring sites over the last two
decades since PM2.5 measurements
consequences of industrial, governmental, and
commercial operations or programs and policies.’’
165 Design value is defined in § 58.1 as the
calculated concentration according to the
applicable appendix of 40 CFR part 50 for the
highest site in an attainment or nonattainment area.
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commenced nationally in 1999.166 This
downward trend has resulted in lower
background concentrations being
measured upwind of urban areas;
however, the impact of local emissions
on PM2.5 may not be known if there is
not a requirement to monitor ambient
air in these areas. For example, the
presence of new local sources of fine
particle air pollution proximate to atrisk communities, such as significant
increases in heavy duty truck traffic
since monitors were originally sited,
should be taken into consideration. As
explained in the PA (U.S. EPA, 2022b),
measured PM2.5 at near-road monitoring
stations include an increment relative to
other sites in the same CBSA. The nearroad sites will complement any new or
moved sites located to specifically
address at-risk communities near
sources of concern. We anticipate the
significance of local emissions may
increase if, as proposed, the level of the
annual PM2.5 NAAQS is lowered. Thus,
the EPA seeks to support communities
with at-risk populations in proximity to
local sources of concern so that they
have access to PM2.5 NAAQScomparable data to ensure compliance
with the PM2.5 NAAQS and for other
data uses.
To successfully select and deploy an
ambient air monitoring station,
monitoring agencies must comply with
the requirements of the EPA network
design criteria (40 CFR part 58,
appendix D, section 4.7), consider input
from the community and other
interested stakeholders, and then
overlay the requirements and input with
logistically available options in the
neighborhoods they intend to monitor.
Often, monitoring agencies partner with
schools and other government agencies
that have access to property in a
neighborhood so that the desired
monitoring stations can be sited,
deployed, and maintained. Locating
monitoring stations in neighborhoods
should be done in a way that provides
a good representation of the particulate
matter exposures of the communities in
which they are located. Alternatively,
monitoring stations can be located
directly next to emission sources of
concern. However, these locations,
known as ‘‘source-oriented’’ sites, may
not necessarily represent the exposures
in community or the effect of a
multitude of emissions that can impact
a neighborhood.
To ensure monitoring sites are
appropriately representing exposure in
at-risk communities, we propose that
sites represent ‘‘area-wide’’ air quality
166 See: https://www.epa.gov/air-trends/
particulate-matter-pm25-trends.
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near local sources of concern. Sites
representing ‘‘area-wide’’ air quality are
those monitors sited at neighborhood,
urban, and regional scales, as well as
those monitors sited at either micro- or
middle-scale that are identified as being
representative of many such locations in
the same Metropolitan Statistical Area
(MSA).167 Most existing as well as new
or moved sites are expected to be
neighborhood-scale, which means that
the monitoring stations would typically
represent conditions throughout some
reasonably homogeneous urban subregion with dimensions of a few
kilometers [part 58, appendix D, section
4.7.1(c)(3)]. Additionally, as described
in § 58.30, sites representing ‘‘areawide’’ air quality have a long-standing
applicability to both the annual and 24hour PM2.5 NAAQS. Siting in a
community representing ‘‘area-wide’’ air
quality as proposed is consistent with
other network design objectives
pursuant to which we locate monitors
where people live, work, and play.
The types of sites that are minimally
required as part of the PM2.5 network
design are associated with two
geopolitical levels: MSAs and states.
The minimum number and type of sites
that are required within an MSA are a
function of the population of the MSA,
based on the latest available information
from the Census Bureau, and the design
value of the existing network of PM2.5
sites reported for that MSA. MSAs with
design values at or above 85% of any
PM2.5 NAAQS are required to operate
one more site than those MSAs with
values that are less than 85% of any
PM2.5 NAAQS (40 CFR part 58,
appendix D, Table D–5). Each MSA
required to operate at least one
monitoring station is to site the monitor
at neighborhood or larger scale in an
area of expected maximum
concentration. MSAs with a population
of 1 million or more are required to
operate a PM2.5 monitor at a NO2 nearroad station in the same MSA. Thus,
according to Table D–5 of appendix D
to part 58, only those MSAs with a
population of greater than 1 million
with the most recent 3-year design value
greater than or equal to 85% of any
PM2.5 NAAQS are required to operate at
least three PM2.5 monitoring stations.
Since one of these sites would be the
site in the area of expected maximum
concentration, which most often will be
the design value site, and the other the
near-road site, only the third location
167 MSA means a CBSA associated with at least
one urbanized area of 50,000 population or greater.
The central-county, plus adjacent counties with a
high degree of integration, comprise the area.
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would not address either of those two
requirements.
The requirement for a third
monitoring station in a MSA, where it
exists, would take on the revised
network design requirement to address
at-risk communities near sources of
concern. Many existing sites in the area
of expected maximum concentration or
near-road sites that are located in at-risk
communities. Thus, having multiple
sites located in at-risk communities may
be appropriate so long as each siting
criteria is achieved. Also, while we are
proposing this modification to our
network design criteria, we recognize
that the number of monitors to support
key monitoring objectives, including
addressing at-risk communities, could
go well beyond what is currently
minimally required. Many monitoring
agencies already operate more
monitoring sites than are minimally
required and we expect this to continue
in considering siting monitors in at-risk
communities. Thus, the existing and
robust network of almost 1,000 PM2.5
sites nationally will continue to protect
all populations at the level of the
NAAQS discussed in section II of this
proposal, by always having at least one
site in the area of expected maximum
concentration for each CBSA where
monitoring is required. Many existing
and a few new sites will form an
important sub-component of the PM2.5
network by characterizing air quality in
at-risk communities, particularly with
respect to sources of concern.
Monitoring requirements applicable at
the state level include measuring
regional background and regional
transport (40 CFR part 58, appendix D,
section 4.7.3). These required sites at
the state level are largely located in
rural areas and may include use of
IMPROVE samplers or continuous PM2.5
monitors. The sites required at the state
level complement sites required at the
MSA level. Together the sites already
required at the state level combined
with existing siting requirements at the
MSA level as well as the proposed
revisions described herein to address atrisk communities will achieve several
monitoring objectives, including
comparison to the NAAQS and AQI.
The availability of data from regional
background and regional transport sites
compared to data from design value
sites already allow for calculating
incremental exposure in communities
with the highest design value location.
With the proposed addition of a siting
requirement for at-risk communities and
the use of data from these sites
compared to select regional background
and regional transport sites as well as
other sites in the same MSA, we can
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assess the incremental burden of
exposure from local emissions to at-risk
communities.
In addition to using data from the
robust network of almost 1,000 PM2.5
sites for NAAQS and AQI purposes,
having a stable network of long-term
sites is especially valuable for trends
and as an input to long term health and
epidemiology studies that support
reviews of the PM NAAQS. Therefore,
while we are proposing to add a PM2.5
network design criteria to address atrisk communities, many sites are likely
already in valuable locations meeting
one of the existing network design
criteria (i.e., being in an area-wide area
of expected maximum concentration or
collocated with near-road sites) and
supporting multiple monitoring
objectives. Also, in many communities
there may already be sites meeting the
network design criteria we are
proposing for at-risk communities.
Thus, acknowledging the value of
having long-term data from a consistent
set of network sites, on balance the EPA
believes that the movement of sites
should be minimized, especially in
MSA’s with a small number of sites.
However, a small number of new
sites 168 are expected to be required due
to the existing minimum monitoring
requirements (Table D–5 of appendix D
to part 58) and the revised primary
annual PM2.5 NAAQS proposed in
section II of this proposal. Also, sites do
on occasion need to move due to loss of
leases, no longer meeting siting criteria,
or other reasons. For any of these cases,
we believe it is appropriate to include
prioritizing establishing sites in at-risk
communities near sources of concern,
should new sites be established, or
existing locations be lost, and
replacement sites need to be identified.
Therefore, the EPA proposes that annual
monitoring network plans [40 CFR
58.10(a)(1)] that include the few newly
required sites and five-year assessments
[40 CFR 58.10(d)] include a provision to
examine the ability of existing and
proposed sites to support air quality
characterization for areas with at-risk
populations in the community and the
objective discussed herein.
Assessing and prioritizing at-risk
communities for monitoring can be
accomplished through several
approaches. The most critical aspect of
prioritizing which communities to
168 Gantt, B. (2022). Analyses of Minimally
Required PM2.5 Sites Under Alternative NAAQS.
Memorandum to the Rulemaking Docket for the
Review of the National Ambient Air Quality
Standards for Particulate Matter (EPA–HQ–OAR–
2015–0072). Available at: https://
www.regulations.gov/docket/EPA-HQ-OAR-20150072.
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monitor is their representation of the atrisk populations described earlier in this
section. The other major consideration
is whether the community is near
source(s) of concern. While many
CBSA’s have one or more sources of
concern described above, some CBSA’s
will not have the level of emissions
from sources of concern that result in an
elevated level of measured PM2.5
concentrations in surrounding
communities. Since one of our other
siting criteria to ‘‘. . . be in the area of
expected concentration’’ [§ 58.1 and
appendix D, section 4.7.1(b)(1)] ensures
there is a monitoring site in the
community with the highest exposure in
each CBSA with a monitoring
requirement, on balance the EPA
believes we should include being in an
at-risk community for CBSAs with a
third site requirement when there are no
sources of concern identified in a CBSA
or such sources do exist but are not
expected to lead to elevated levels of
measured PM2.5 concentrations.
To identify at-risk communities to
consider for the proposed monitoring
requirement, tools such as the EPA’s
EJSCREEN 169 are available. The EPA
solicits comment on other tools and/or
datasets that can could be utilized to
identify the at-risk communities
described above. With information on
at-risk communities, monitoring
agencies need data that can best inform
where there may be elevated levels of
exposures from sources of concern.
While we use FRMs and FEMs to
determine compliance with the NAAQS,
there are several additional datasets
available that may be useful in
evaluating the potential for elevated
levels of exposure to communities near
sources of concern. Potential datasets
include non-regulatory data (CSN,
IMPROVE, and AQI non-regulatory
PM2.5 continuous monitors), modelling
data—which utilizes emission inventory
and meteorological data, emerging
sensor networks such as used in the
EPA’s AirNow fire and smoke map,170
and satellites—which measure radiance
and with computational algorithms are
then used to estimate PM2.5 from aerosol
optical depth (AOD). The 2019 ISA and
PA (U.S. EPA, 2019a; U.S. EPA, 2022b)
include details on each these, except for
the AirNow fire and smoke map, which
first became operational in 2020. Each
of these datasets have advantages and
disadvantages, especially when
attempting to determine exposure
concentrations for the averaging times of
the PM2.5 NAAQS described in section
II (i.e., annual NAAQS and 24-hour
169 See:
170 See:
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5675
NAAQS). The EPA solicits comment on
datasets most useful to identify
communities with high exposures for
PM2.5 NAAQS (i.e., annual or 24-hour),
including any discussion on limitations
or advantages of the dataset of interest.
The EPA is soliciting comment on the
use of these datasets for the purpose of
identifying communities where the
proposed monitoring requirement
would apply and not for the purpose of
satisfying the proposed monitoring
requirement.
The monitoring methods appropriate
for use at these proposed sites are FRMs
and automated continuous FEMs. These
are the methods that are eligible to
compare to the PM2.5 NAAQS, which
will be the primary objective for
collecting this data. There are several
other monitoring objectives that would
benefit from use of automated
continuous FEMs. For example, having
hourly data available from automated
continuous FEMs would allow sites to
provide data in near-real time to support
forecasting and near real-time reporting
of the AQI. Automated continuous
methods are also useful to support
evaluation of other methods such as
low-cost sensors. When used in
combination with on-site wind speed
and wind direction measurements,
automated FEMs can provide useful
pollution roses indicating the origin of
emissions that affect a community.
Additionally, when collocated with
continuous carbon methods such as an
aethalometer, automated FEMs can help
identify potential local carbon sources
contributing to increased exposure in
the community. The EPA and the
CASAC worked collaboratively in 2010
(Russell and Samet, 2010) to define a
list of measurements that would be
useful to implement in the near-road
environment, and a subset of these
measurements may additionally be of
value to characterize the exposure in atrisk communities. While either FRMs or
automated FEMs may be used at a site
for comparison to the PM2.5 NAAQS, the
EPA encourages use of automated
continuous FEMs at sites in at-risk
communities.
Although there are only a few new
sites required,171 plus any potentially
moved sites in cases where a site lease
is lost, EPA believes we should build
upon our existing regulatory process for
selecting and approving these sites (40
171 Gantt, B. (2022). Analyses of Minimally
Required PM2.5 Sites Under Alternative NAAQS.
Memorandum to the Rulemaking Docket for the
Review of the National Ambient Air Quality
Standards for Particulate Matter (EPA–HQ–OAR–
2015–0072). Available at: https://
www.regulations.gov/docket/EPA-HQ-OAR-20150072.
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CFR 58.10). For example, the timeline to
implement the proposed PM2.5 sites in
at-risk communities should allow
monitoring agencies enough time for
communities and other interested
parties to provide their input regarding
moving or adding new sites, while also
minimally disrupting ongoing
operations of monitoring agency
programs. Another important factor is to
ensure all existing PM2.5 sites have data
available for comparison to a revised
PM2.5 NAAQS, which is discussed in
section II of this proposal. With a final
rule from this proposal expected in
2023, we believe it would be
appropriate to provide at least 12
months from the effective date of a final
rule for monitoring agencies to initiate
planning to implement these measures
by seeking input from communities and
other interested parties, and to consider
revisions to their PM2.5 networks or
explain how the existing network meets
the objectives of this proposed
modification. Thus, the EPA proposes
that monitoring agencies identify their
initial approach to the question of
whether any new or moved sites are
needed and to identify the potential
communities in which the agencies are
considering adding monitoring, if
applicable, as well as identifying how
they intend to meet the proposed
revised criteria for PM2.5 network design
to address at-risk communities. These
aspects that will potentially affect the
siting of new and moved sites should be
addressed in the agencies’ annual
monitoring network plans due to each
applicable EPA Regional office no later
than July 1, 2024 (40 CFR 58.10).
Specifics on the resulting proposed new
or moved sites for PM2.5 network design
to address at-risk communities would
need to be detailed in the annual
monitoring network plans due to each
applicable EPA Regional office no later
than July 1, 2025 (40 CFR 58.10). We are
proposing that any new or moved sites
would be required to be implemented
and fully operational no later than 24
months from the date of approval of a
plan or January 1, 2027, whichever
comes first, but the EPA solicits
comment on whether less time is
needed (e.g., 12 months from plan
approval and/or January 1, 2026).
In summary, the EPA is proposing to
modify our PM2.5 network design
criteria to include an environmental
justice factor to address at-risk
communities with a focus on exposures
from sources of concern. While this
proposal would require that sites be
located in at-risk communities,
particularly those whose air quality is
potentially affected by local sources of
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concern, such sites should still meet the
requirement for being considered ‘‘areawide’’ air quality. Specific areas of
interest we seek comment on include
how to identify at-risk communities, the
sources of concern important to
consider, the datasets to identify
communities with high exposures, and
the most useful measurements to
collocate with PM2.5 in at-risk
communities. The EPA seeks comment
on these areas of interest as well as the
proposed modification of our PM2.5
network design objectives and
implementation as described herein.
5. Proposed Revisions to Probe and
Monitoring Path Siting Criteria
The EPA is proposing changes to
monitoring requirements in the
Appendix E—Probe and Monitoring
Path Siting Criteria for Ambient Air
Quality Monitoring. Since 2006,
multiple rule revisions were made to
establish siting requirements for
PM10–2.5 and O3 monitoring sites (71 FR
2748, January 17, 2006), Near-Road NO2
monitoring sites (75 FR 6535, February
9, 2010), Near-Road CO monitoring sites
(76 FR 54342, August 31, 2011), and
Near-Road PM2.5 monitoring sites (78 FR
3285, January 15, 2013). Through these
multiple revisions to the regulatory text,
some requirements were inadvertently
omitted, and, over time, the clarity of
this appendix was reduced through
these omissions that, in a few instances,
led to unintended and conflicting
regulatory requirements. The EPA
proposes to reinstate portions of
previous Probe and Monitoring Path
Siting Criteria Requirements from
previous rulemaking where appropriate
to restore the original intent. The
proposed changes that affect the overall
appendix follow, while those specific to
the various sections of the appendix
will be addressed under a specific
section heading. The EPA notes that
appendix E is being reprinted in its
entirety with this proposal because this
section is being reorganized for clarity
in addition to being selectively revised
as described in detail below. The EPA
is soliciting comment on the specific
provisions of appendix E proposed for
revision. However, there are a number
of provisions that are being reprinted
solely for clarity to assist the public in
understanding the changes being
proposed and reconciling requirements
between different portions of the text;
the EPA is not soliciting comment on
those provisions and considers changes
to those provisions to be beyond the
scope of this proposed rulemaking.
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a. Providing Separate Section for Open
Path Monitoring Requirements
The current appendix E regulation
combines open path monitor siting
requirements with requirements for
siting samplers and monitors that utilize
probe inlets. While this approach
allowed the EPA to promulgate an
abbreviated regulation for probe-siting
requirements, the EPA now has
determined that the clarity of the
requirements for each monitoring
method type has been diminished by
this combination. As such, the EPA is
proposing to relocate all open path
monitor siting criteria requirements to a
separate section in this appendix.
Providing separate sections for these
distinct monitoring method types will
allow the EPA to more clearly articulate
minimum technical siting requirements
for each. Further rationale for creating
these separate sections is that the
regulatory monitoring community has
not submitted to AQS measurement
results from open path monitors since
2009. Because these open path
monitoring methods are rarely used for
monitoring to compare to the NAAQS,
the EPA believes that moving the open
path siting criteria to their own section
will make clearer the probe siting
criteria for the ambient air monitoring
methods that are now most commonly
utilized by monitoring organizations.
b. Amending Distance Precision for
Spacing Offsets
The EPA proposes to require that
when rounding is performed to assess
compliance with these siting
requirements, the distance
measurements will be rounded such as
to retain at least two significant figures.
The EPA proposes to communicate this
rounding requirement in the regulatory
text using footnotes in Table E–1, Table
E–2, and Table E–3 of the current
regulation.
c. Clarifying Summary Table of Probe
Siting Criteria
To provide additional specificity and
flexibility to the summary table for
probe siting criteria (see current Table
E–4 in appendix E), the EPA proposes
to change the ‘‘>’’ (greater than) symbols
to ‘‘≥’’ (greater than or equal to)
symbols. This minor revision will more
clearly express the EPA’s intent that the
distance offsets provided in the current
Table E–4 in appendix E are acceptable
for NAAQS compliance monitoring.
d. Adding Flexibility for the Spacing
From Minor Sources
Current requirements for the spacing
of probe inlets and monitoring paths
from minor sources of SO2 and NO2
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stipulate that the probe inlets and
monitoring paths must be away from
these minor sources (see current section
3(b) in appendix E). The EPA proposes
to clarify and provide flexibility by
changing this requirement to a goal. The
EPA proposes to replace the ‘‘must’’ in
this regulation with a ‘‘should’’. As
stated in section 1(c) of the current rule,
a ‘‘must’’ defines a requirement while a
‘‘should’’ specifies a goal. Since the
current rule does not specify how far the
probe must be spaced from such minor
sources, the EPA proposes that a
‘‘should’’ in this regulation is more
appropriate. Minor sources can have
adverse impacts on the
representativeness of the ambient
pollutant concentrations sampled by the
probe inlet. As such, the EPA
recommends that sites with these minor
sources be avoided whenever
practicable and probe inlets spaced as
far from these minor sources as possible
when alternative monitoring stations are
not suitable.
e. Amendments and Clarification for the
Spacing From Obstructions and Trees
The EPA proposes to clarify and
redefine that the minimum arc required
to be free of obstructions for a probe
inlet or monitoring path is 270 degrees.
Currently this portion of the regulation
(see current section 4(b) of appendix E)
specifies 180 degrees as this minimum
arc. However, this requirement is
inconsistent with the requirement found
in footnote 5 of Table E–4 in appendix
E that specifies the probe inlet or
monitoring path must have unrestricted
airflow of 270 degrees around the probe
and 180 degrees for the arc is only
allowed if the probe is on the side of a
building or a wall. These inconsistent
regulatory requirements were
introduced in the 2006 rulemaking
when the 270-degree requirement was
omitted from the text of section 4(b) (see
71 FR 61236, October 17, 2006).
There are also inconsistent
requirements in the current regulation
regarding the spacing of probe inlets
from the driplines of trees. Section 5(a)
of appendix E requires the probe inlet
must be no closer than 10 meters to the
driplines of any trees, while footnote 3
of Table E–4 of the appendix E qualifies
that this minimum 10-meter offset is
only required when the tree also acts as
an obstruction.
f. Reinstating Minimum 270-Degree Arc
and Clarifying 180-Degree Arc in
Regulatory Text
The EPA proposes to correct
identified inconsistencies in this
regulation by reinstating the 270-degree
requirement in section 4(b) of appendix
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E. Additionally, the EPA proposes to
further clarify this regulation by stating
that the continuous 180-degree
minimum arc of unrestricted airflow
provision is reserved for monitors sited
on the side of a building or a wall to
comply with network design criteria
requirements specified in appendix D of
part 58. Examples include CO
monitoring in urbanized areas that relies
on monitoring in street canyons and
near-road monitoring where a
continuous arc of 270 degrees of
unrestricted airflow is not routinely
possible given limited monitor siting
options.
g. Clarification on Obstacles That Act as
an Obstruction
The EPA proposes to clarify the
definitions of ‘‘obstructions’’ and
‘‘obstacles’’ in the regulatory text (see
section 4 of the current appendix E).
While obstacles should be avoided as
much as is practicable, logistical
constraints may dictate that some
obstacles are present within the vicinity
of the monitoring probe inlet.
Obstructions to the air flow of the probe
inlet are those obstacles that are
horizontally closer than twice the
vertical distance the obstacle protrudes
above the probe inlet and can be
reasonably thought to scavenge reactive
gases or to restrict the airflow for any
pollutant. The EPA does not generally
consider objects or obstacles such as flag
poles or site towers for NOy convertors
or towers for meteorological sensors,
etc. to be obstructions.
h. Amending and Clarifying the 10Meter Tree Dripline Requirement
The EPA proposes to reconcile the
conflicting requirements in section 5(a)
and Table E–4, footnote 3 of the current
regulation by deleting the qualification
in footnote 3 of Table E–4 to require that
the probe inlet must always be no closer
than 10 meters to the tree dripline. The
EPA also proposes to reinstate the goal
that was omitted from section 5(a)
during previous rule revisions, that
monitor probe inlets should be at least
20 meters from the driplines of trees.
Additionally, the EPA proposes to
clarify section 5(a) of the current
regulation by adding that when the tree
or group of trees is considered an
obstruction, then the regulatory
requirements of section 4(a) apply.
i. Amending Spacing Requirement for
Microscale Monitoring
To obtain representative ambient air
monitoring measurements for sourceoriented and microscale air monitoring
stations, it is important to have
unobstructed airflow between the
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monitor’s probe inlet and the source
under investigation. This reasoning was
used by the EPA when near-road NO2
monitoring stations were required to
have an unobstructed airflow between
the monitor probe and the outside
nearest edge of the traffic lane (see
current section 4(d) of this regulation).
To assist in further clarifying the
monitoring siting criteria for the spacing
from obstructions and spacing from
trees, the EPA proposes to change from
a goal to a requirement that microscale
sites for any pollutant shall have no
trees or shrubs blocking the line-of-sight
fetch between the monitor’s probe inlet
and the source under investigation. The
EPA proposes to communicate this
requirement by changing the ‘‘should’’
to a ‘‘shall’’ in the regulatory text of
section 5(c). The EPA does not consider
small obstacles such as shrubs that are
below this fetch to adversely impact the
representativeness of the air quality
measurements results. This proposed
revision of section 4(d) will bring more
consistency to appendix E.
j. Amending Waiver Provisions
The EPA believes the effects of any
requirements in this proposal that may
be considered to be new are minor.
While we are attempting to clarify probe
and siting criteria as part of our
monitoring regulations, the Agency fully
intends to maintain waiver provisions
that exist in the regulation for these
siting criteria (see current section 10).
For cases where long-term trend sites or
monitors that determine the design
value for their area cannot reasonably
meet these regulatory siting
requirements, the EPA encourages
monitoring organizations to work with
their respective EPA Regional Offices to
determine if a waiver from these siting
criteria is appropriate.
Even though the current regulation
adequately and clearly identifies which
monitoring situations are eligible for the
EPA to consider waiving the
requirements for probe-siting criteria
(see current section 10), these waiver
provisions are silent regarding how long
an approved waiver remains in force
and effect. Environmental conditions
(e.g., airflow due to changes in growth
of trees, shrubs, construction of
buildings or other obstructions) around
monitoring stations are prone to change
over time. As such, the EPA has
identified that previously approved
waivers should be periodically
reevaluated to ensure that the
conditions upon which the original
waiver was approved still exist and that
the siting conditions have not degraded
to an unacceptable level. The EPA
proposes to modify section 10.3 of the
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current regulation to state that waivers
from the probe-siting criteria must be
renewed minimally every 5 years.
Ideally, sites needing a waiver renewal
should be inspected by the EPA such as
during a Technical Systems Audit (TSA)
typically conducted at a subset of sites
within each Primary Quality Assurance
Organization (PQAO) every three years.
However, virtual inspections may also
be acceptable using documentation such
as photos and traffic counts. Dates for
the most recent approval of a waiver
must then be included in the applicable
network assessment and annual
monitoring network plan. The EPA
proposes to revise § 58.10(b)(10) of the
regulation to maintain consistency in
the text for probe siting criteria
requirements and annual monitoring
network plans. This proposal leverages
the existing annual assessment
requirements found in § 58.10(a)(1) and
(d).
k. Broadening of Acceptable Probe
Materials
The current regulatory specifications
for acceptable probe materials for
sampling reactive gases are limited to
borosilicate glass, fluorinated ethylene
propylene (FEP) Teflon®, or their
equivalent (see section 9 of the
regulation). The EPA’s selection of ‘‘or
its equivalent’’ in the current regulatory
text was intended to allow flexibility to
monitoring organizations when
selecting suitable sampling train
materials. In practice, however, this text
has resulted in potentially suitable
materials not being used for sampling
trains due to concerns that the material
may not meet these regulatory
requirements. The current requirements
for acceptable probe materials were
promulgated in 1979. Since 1979,
several potential alternatives to
borosilicate glass and FEP were
developed and are commercially
available.
Because some of these alternative
materials have advantages over the
currently approved materials (e.g., cost
and durability), the EPA has received
numerous inquiries from monitoring
organizations regarding the regulatory
suitability of these materials.
Monitoring organizations have
expressed particular interest in the
potential use of PVDF (polyvinylidene
fluoride) which is marketed under the
registered tradename of Kynar® by
Arkema Inc. (Colombes, France). In
response to these inquiries, the EPA’s
Office of Research and Development
(ORD) recently designed and conducted
a laboratory study to determine the
transport efficiency of O3, SO2, NO2, and
CO through several candidate tubing
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materials (Johnson, 2022). Based on
these tests results, the EPA is proposing
to revise Section 9 of the current
regulation to add polyvinylidene
fluoride (PVDF), polytetrafluoroethylene
(PTFE), and perfluoroalkoxy (PFA) to
the list of approved materials for
efficiently transporting gaseous criteria
pollutants. The EPA also proposes to
clarify that the residence-time criteria
for sampling reactive gas through these
approved materials applies to all O3,
SO2, and NO2 monitors. In conjunction
with the previously approved
borosilicate glass and FEP materials,
including these three new materials
would provide monitoring organizations
with a wider variety of efficient
sampling and transport materials
needed for conducting NAAQS
compliance monitoring.
The EPA has also studied and
approved the use of NafionTM upstream
of ozone analyzers to minimize
measurement bias associated with high
ambient RH levels (U.S. EPA, 2020b).
Minimal loss of ozone occurred in these
systems as long as the NafionTM system
was conditioned beforehand. NafionTM
is composed primarily of PTFE and can
be considered equivalent to PTFE. It has
been shown in ORD’s recent tests
described above to exhibit virtually no
loss of ozone at 20 second residence
times.
D. Taking Comment on Incorporating
Data From Next Generation
Technologies
1. Background on Use of FRM and FEM
Monitors
The EPA approves FRM and FEM
monitors for criteria pollutant
measurements in the Federal Register
after careful review of applications
describing extensive testing of the
methods operation and performance.
The siting of these monitors across
State, local, and Tribal networks is
subject to detailed requirements for
network design detailed in appendix D
to 40 CFR part 58 with probe and siting
criteria described in appendix E for 40
CFR part 58. The operation of these
monitors is subject to extensive quality
assurance requirements detailed in
appendix A to 40 CFR part 58, which
ensures data quality statistics are
produced to inform the quality of the
data needed to ensure regulatory grade
decisions are made with data of known
quality. The EPA believes these
requirements are important for ensuring
the degree of accurate and precise data
which is appropriate for regulatory
decision-making, particularly decisions
about attainment or nonattainment of
the NAAQS. However, the EPA also
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recognizes that the capital and operating
costs of these monitors is substantial,
which requires the EPA and states to
prioritize where monitors should be
deployed. The EPA recognizes that
making use of broader air quality data
sets which are less expensive can
provide important benefits, even if the
EPA does not consider those datasets
suitable for all regulatory purposes. In
some circumstances in the past, for
example, the EPA has used non-FRM
monitoring to inform decisions about
the boundaries of a nonattainment area,
although the data was not sufficient to
support a finding that an area was in
nonattainment. Likewise, the EPA has
incorporated sensor data into its fire and
smoke map for the purpose of informing
the public of potential imminent health
risks, even though that data would not
be comparable to the NAAQS for
purposes of determining attainment.
There are multiple uses of air quality
data and the EPA believes there may be
additional opportunities to develop
broader air quality datasets which
provide benefits to the EPA and the
public even where the data is not from
FRM/FEM monitors and is not suitable
for comparison to the NAAQS.
2. Next Generation Technologies: Data
Considerations
The EPA and our State, local, and
Tribal partners in cooperation with
other Federal agencies have made great
strides in integrating data from routine
air monitoring methods with data from
next generation technologies to address
emerging air quality issues. For
example, the EPA and U.S. Forest
Service (USFS), in consultation with
other partners, launched the publicly
available AirNow Fire and Smoke
Map,172 which has received over 26
million page views since its release in
July 2020. This fire and smoke map has
been an invaluable tool for the public,
providing refined spatial information on
current Air Quality Index (AQI)
conditions, fire and smoke plumes
locations, actions for communities to
take based on local air quality, and links
to Smoke Forecast Outlooks developed
by specially trained air resource
advisors. Data are brought together from
multiple systems including permanent
and temporary PM2.5 continuous
monitoring sites, sensors, and satellite
derived fire and smoke data. With the
success of the fire and smoke map and
a robust and growing network of PM2.5
continuous FEMs and sensor network
data, as well as existing and future
satellites products, the EPA is interested
in considering further enhancements to
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the evolution of data products to meet
new and emerging non-regulatory air
quality data needs. Below we describe
each of the major data sets, their
advantages, and any challenges to their
use. We then solicit input on additional
approaches and/or products to
incorporating data from next generation
technologies that can help address
important non-regulatory air quality
data needs.
3. PM2.5 Continuous FEMs
As described in the PA, State, local,
and Tribal monitoring agencies are
using an increasing number of PM2.5
continuous FEMs. These methods are
primarily deployed to meet two
monitoring objectives: first, to compare
to the NAAQS, and second, to report
and support forecasting of the AQI.
PM2.5 continuous FEMs have some key
advantages over FRMs, most notably
that they provide automated hourly
measurement of PM2.5 available in near
real time. The continuous PM2.5 data are
reported as soon as practicable after the
end of each hour, usually within 5–10
minutes, and are used in multiple
applications of real-time data such as
such as by State, local, and Tribal
websites,173 174 the EPA’s AirNow
website, and national media outlets.
Recent improvements in the availability
and exchange of near real-time data
through a dedicated AirNow
Application Programming Interface
(API) allow for efficient exchange of
data between the EPA, other Federal
agencies, and commercial data
providers such as low-cost sensor
networks. The efficient exchange of data
through the AirNow API was a key
advancement in the successful
implementation of the EPA AirNow’s
fire and smoke map. The PM2.5
continuous FEM data are critical to
‘‘ground truthing’’ other datasets such as
sensors and satellites for two important
reasons. First, PM2.5 continuous FEMs
are subject to extensive regulatory-grade
quality assurance and quality control as
required by appendix A to 40 CFR part
58. Second, PM2.5 continuous FEMs are
located in accordance with strict siting
criteria according to appendix E to 40
CFR part 58. The siting criteria assure
that measured data represent ambient
air at ground level where people are
breathing and are thus exposed to
particle pollution. The EPA and State,
local, and Tribal agencies are working to
upgrade many existing FRM-only sites
with PM2.5 continuous FEMs through
173 See: https://www.airnow.gov/partners/stateand-local-partners/.
174 See: https://www.airnow.gov/partners/tribalpartners/.
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use of American Rescue Plan funds.175
Despite these investments, there are
major challenges to monitoring
agencies’ ability to have enough trained
and available staff to support their
regulatory monitoring networks,
especially in remote locations, and to
have the capital resources to implement
new monitoring stations. So, while there
may be some improvements to the
existing network of almost 1,000 PM2.5
regulatory-grade monitoring stations,
regulatory instruments will not produce
data everywhere that it is desired. Thus,
the integration of PM2.5 continuous
FEMs with other datasets is an
important opportunity to address
existing and emerging air quality data
needs for non-regulatory purposes.
4. PM2.5 Satellite Products
Satellite-based instruments provide
measurements of radiance that can be
used to calculate the aerosol optical
depth (AOD) of the atmosphere. For
over a decade, satellite AOD values have
been used in models that incorporate
multiple datasets to predict surface level
PM2.5 concentrations over the U.S.
(hereafter, satellite-PM2.5). Despite some
heterogeneity in performance under
varying conditions, the satellite-PM2.5
datasets have significantly advanced in
terms of accuracy in recent years (Di et
al., 2019; van Donkelaar et al., 2019;
Zhang and Kondragunta, 2021). The
EPA is using satellite-PM2.5 datasets in
a variety of contexts. Satellite-PM2.5 data
was included in a comparative analysis
of hybrid modeling methods in the PA
(U.S. EPA, 2022b). The EPA is also
working with the National Aeronautics
and Space Administration (NASA) and
National Oceanic and Atmospheric
Administration (NOAA) to use satellitePM2.5 in the AirNow system.176 The
EPA also uses satellite AOD and many
other satellite data products in the
development of our photochemical
modeling platforms that are used in
regulatory and policy assessments both
by the EPA and by our State and local
partners.
Each satellite data product has its
own strengths and limitations. One
strength is the spatial coverage, which
can be once-a-day globally for polar
orbiting satellites or over a fixed field of
view continuously for geostationary
satellites. Satellite-PM2.5 data has the
limitation that it is not a direct
measurement of PM2.5 concentrations,
175 See: https://www.epa.gov/arp/enhanced-airquality-monitoring-funding-under-arp.
176 The EPA provided an update on the Health
and Air Quality Applied Scientist Team (HAQAST)
AirNow Project at the NASA HAQAST meeting in
Texas in June 2022. For more information, see:
https://haqast.org/haqast-houston-june-1-2/.
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but rather is derived through a model
that connects the total column AOD to
surface PM2.5. In addition, the satellite
products are only capable of making
daytime measurements because they
rely on sunlight. In fact, most satellitePM2.5 data products use the surface
monitor network as an input. As such,
the satellite-PM2.5 data does not
substitute for a ground-based monitor;
rather it complements the monitor
network. The EPA continues to explore
ways to use the wealth of data from
satellites to address important air
quality questions consistent with their
strengths and limitations.
5. Use of Air Sensors
The term ‘‘air sensor’’ is a simplified
way of referring to a class of technology
that has expanded on the market in
recent years and has common traits of
directly reading a pollutant in the air,
being smaller in size, and often sold at
lower prices that support a wider
number of monitoring locations than
possible in the past. As explained on the
EPA’s Air Sensor Toolbox website,177
air sensor monitors that are lower in
cost, portable, and generally easier to
operate than regulatory-grade monitors
are widely used in the United States to
understand air quality conditions. Many
refer to this class of technology as ‘‘lowcost air sensors,’’ ‘‘air sensor devices,’’
or ‘‘air quality sensors.’’ Potential uses
for these non-regulatory air sensor
technologies include, but are not limited
to, science education, supplementing
regulatory air quality measurements,
conducting research, measuring local air
quality to better understand sources of
pollution, locating leaks at industrial
facilities, and emergency response.
The growth in use of sensors included
in the EPA’s fire and smoke map
provides a platform to build upon.
There are thousands of PM sensors
whose data are coordinated and overlaid
with routine and temporary PM2.5
continuous monitors as well as satellitederived data on fires and smoke.
Sensors offer an opportunity to
supplement higher-cost regulatory
monitoring to provide data for the nonregulatory uses as described above.
However, there are several challenges to
using sensors. Each commercially
available PM sensor appears to have its
own data quality challenges depending
on season, aerosol encountered, and
meteorological conditions (typically
temperature and relative humidity). The
EPA has gone to considerable length to
ensure the PM2.5 sensor data on the fire
and smoke map have a correction
available with collocated FRMs and
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FEMs.178 This was possible due to the
large number of air sensors that are the
same make and model located across the
country. Thus, an important challenge
for the use of sensors is the spatial
richness in sensor networks needed to
make integrating the dataset with other
monitoring data viable. Even with
corrected sensor data in hand, publicly
shared sensor data lacks reliability and
accountability for ensuring that basic
siting criteria are met. Sensors are often
installed by members of the public who
share data to the sensor network, which
is generally understood as implicitly
representing that the sensor is located in
ambient air although, in fact, the sensor
may be located inside a home or next to
a highly localized source of emissions
such as the flue of a home heating
system. In areas with many reporting
sensors, these concerns about siting may
be lessened through site-to site
comparison of data; however, the
absence of any confirmed information
about siting presents challenges for use
of sensor data.
6. Summary
The near real-time integration of data
from PM2.5 continuous monitors,
sensors, and satellites has been proven
through use of the EPA’s fire and smoke
map. This mapping product is possible
though the use of API’s where data sets
are automatically shared on prespecified computer servers. Given the
success of the fire and smoke map, the
EPA is interested in pursuing additional
approaches and/or products that can
help address important non-regulatory
air quality data needs. Therefore, the
EPA solicits comment on the most
important data uses and data sets to
consider in future products. Such
approaches and/or products could
utilize historical or near real-time data.
For example, what are the advantages
and disadvantages of using existing data
and tools to identify PM hot spots across
an area of interest? Could satellite data
or a combined surface layer (PM2.5 FRM
and FEM data, sensor data, and satellite
data) be useful in siting regulatory
monitors? Could combined surfaces
layers be useful in determining the
boundaries of nonattainment areas?
Could combined surface layers be useful
in exploring potential emission sources
to consider in SIP planning? To what
extent would requirements for data
formats, units, or timescales of interest
need to evolve to best address these
needs? What other datasets should the
EPA consider merging with the data sets
178 See:
https://www.epa.gov/research-states/
airnow-fire-and-smoke-map-extension-us-widecorrection-purpleair-pm25-sensors.
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listed above to help better inform air
quality management, including
prioritizing network investments for
potential new sites such as in at risk
communities described elsewhere in
this proposal? The EPA seeks input and
prioritization on each of these questions
to help improve the utility of data to
better support air quality management
to improve public health and the
environment.
VIII. Clean Air Act Implementation
Requirements for the PM NAAQS
The proposed revision to the primary
annual PM2.5 NAAQS discussed in
section II above, if finalized, would
trigger a process under which states 179
will make recommendations to the
Administrator regarding area
designations. States also will be
required to review their existing section
110 infrastructure state implementation
plans and modify them if necessary to
implement a revised NAAQS. A revised
primary annual PM2.5 NAAQS will need
to be incorporated into the
implementation of applicable air
permitting requirements and the
transportation conformity and general
conformity processes, and states will
need to review existing regulations for
these programs that already cover PM2.5
to determine the extent to which any
changes are needed. This section
provides background information for
understanding the possible implications
of the proposed NAAQS changes and
describes the EPA’s plans for providing
states guidance needed to assist their
implementation efforts. This section
also describes existing EPA
interpretations of CAA requirements
and other EPA guidance relevant to
implementation of a revised PM2.5
NAAQS. Given the strong scientific
evidence for disparities in PM2.5
exposures and PM2.5-related health risk
among certain populations (as discussed
in section II of this document), the EPA
included in its 2016 PM2.5 State
Implementation Plan (SIP)
Requirements Rule (81 FR 58010,
August 24, 2016) (which was written to
be applicable for any future NAAQS
revisions) included a number of key
recommendations for states to advance
environmental justice through their
attainment planning process. In
addition, as discussed throughout this
section, environmental justice
considerations are evaluated with regard
to the several specific program elements
of the overall implementation process.
179 This and all subsequent references to ‘‘state’’
are meant to include State, local, and Tribal
agencies responsible for the implementation of a
PM2.5 control program.
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State and local air agencies have a
critically important role in
implementing the NAAQS, including
this proposed PM2.5 NAAQS, should it
become finalized. Given the information
provided in this proposed rulemaking,
state and local air agencies are
encouraged to begin to consider how
they might develop implementation
plans that encourage early emission
reductions as well as emission
reductions that facilitate or amplify
reductions affecting overburdened
communities. The public is encouraged
to share information on this important
topic and although this rulemaking is
not requesting comment specifically on
this topic, information on this topic may
be submitted for informational purposes
to the docket for this proposed
rulemaking. The EPA may consider
whether additional guidance on the
topic of environmental justice and PM2.5
implementation is appropriate, beyond
what is already included in the existing
PM2.5 SIP Requirements Rule. The EPA
encourages air agencies and other
stakeholders to review the existing
PM2.5 SIP Requirements Rule and the
information provided therein regarding
environmental justice considerations in
PM2.5 air planning. To be clear, nothing
in the above text should be interpreted
as seeking comment in this proposal on
any aspect of the 2016 PM2.5 SIP
Requirements Rule.
With respect to the topics covered in
this section, the EPA welcomes the
public to provide input to the Agency
through comments. However, because
these issues are not relevant to the
establishment of a revised primary
annual PM2.5 NAAQS, and because no
specific revisions are proposed for the
regulations implementing the PM2.5
NAAQS (i.e., 40 CFR part 51, subpart Z),
the EPA does not expect to respond to
these comments in the final action on
this proposal (nor is it required to do
so).
A. Designation of Areas
After the EPA establishes or revises a
NAAQS, the CAA requires the EPA and
the states to take steps to ensure that the
new or revised NAAQS is met. The first
step, known as the initial area
designations, involves identifying areas
of the country that either meet or do not
meet the new or revised NAAQS, along
with the nearby areas contributing to the
violations.
Section 107(d)(1) of the CAA states
that, ‘‘By such date as the Administrator
may reasonably require, but not later
than 1 year after promulgation of a new
or revised national ambient air quality
standard for any pollutant under section
109, the Governor of each state shall
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. . . submit to the Administrator a list
of all areas (or portions thereof) in the
State’’ and that making
recommendations for whether the EPA
should designate those areas as
nonattainment, attainment, or
unclassifiable.180 The CAA provides the
EPA discretion to require states to
submit their designations
recommendations within a reasonable
amount of time not exceeding 1 year.
The CAA also stipulates that ‘‘the
Administrator may not require the
Governor to submit the required list
sooner than 120 days after promulgating
a new or revised national ambient air
quality standard.’’ Section
107(d)(1)(B)(i) further provides, ‘‘Upon
promulgation or revision of a NAAQS,
the Administrator shall promulgate the
designations of all areas (or portions
thereof) . . . as expeditiously as
practicable, but in no case later than 2
years from the date of promulgation.
Such period may be extended for up to
one year in the event the Administrator
has insufficient information to
promulgate the designations.’’ With
respect to the NAAQS setting process,
courts have interpreted the term
‘‘promulgation’’ to be signature and
widespread dissemination of a final
rule.181 One way the EPA intends to
account for environmental justice in the
implementation process is to promptly
issue designations in accordance with
the statutory requirements to ensure
expeditious public health protections
for all populations, including those
currently experiencing disparities in
PM2.5 exposures and PM2.5-related
health risk.
If the EPA agrees with the designation
recommendation of the state, then it
may proceed to promulgate the
designations for such areas. If, however,
the EPA disagrees with the state’s
recommendation, then the EPA may
elect to make modifications to the
recommended designations. By no later
than 120 days prior to promulgating the
final designations, the EPA is required
to notify states of any intended
modifications to the designations of any
areas or portions thereof, including the
boundaries of areas, as the EPA may
deem necessary. States then have an
opportunity to comment on the EPA’s
tentative designation decision. If a state
elects not to provide designation
recommendations, then the EPA must
timely promulgate the designation that
180 While the CAA says ‘‘designating’’ with
respect to the Governor’s letter, in the full context
of the CAA section it is clear that the Governor
actually makes a recommendation to which the EPA
must respond via a specified process if the EPA
does not accept it.
181 API v. Costle, 609 F.2d 20 (D.C. Cir. 1979)
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it deems appropriate. While section
107(d) of the CAA specifically addresses
the designations process for states, the
EPA intends to follow the same process
for tribes to the extent practicable,
pursuant to section 301(d) of the CAA
regarding Tribal authority, and the
Tribal Authority Rule (63 FR 7254,
February 12, 1998). To provide clarity
and consistency in doing so, the EPA
issued a guidance memorandum to our
Regional Offices on working with tribes
during the designations process (Page,
2011a).
Monitoring data are currently
available from numerous existing PM2.5
Federal Equivalent Methods (FEM) and
Federal Reference Methods (FRM) sites
to determine compliance with the
proposed revised PM2.5 primary annual
NAAQS. As discussed in section II
above, the EPA is proposing to: (1)
revise the level of the primary annual
PM2.5 standard and retain the current
primary 24-hour PM2.5 standard (section
II.D.3); and (2) not change the current
secondary annual and 24-hour PM2.5
standards at this time (section V.D.3).
Consistent with the process used in
previous area designations efforts, the
EPA will evaluate each area on a caseby-case basis considering the specific
facts and circumstances unique to the
area 182 to support area boundaries
decisions for the revised standard.
Section 107(d) explicitly requires that
the EPA designate as nonattainment not
only the area that is violating the
pertinent standard, but also those
nearby areas that contribute to the
violation in the violating area. For the
reason noted earlier, the EPA believes it
is important to consider environment
justice within the framework of this
area-specific analysis. Consistent with
past practice, the EPA expects to
address issues relevant to area
designations more fully in a separate
designations-specific memorandum
around the time of promulgation of any
revised PM2.5 NAAQS.183 Examples of
issues that may be included in the
separate designations-specific
memorandum may include, but are not
limited to, exceptional events
demonstrations for wildfire and/or
prescribed fires on wildland, factors to
182 The EPA has historically used area-specific
analyses to support nonattainment area boundary
recommendations and final boundary
determinations by evaluating factors such as air
quality data, emissions and emissions-related data
(e.g., population density and degree of urbanization,
traffic and commuting patterns), meteorology,
geography/topography, and jurisdictional
boundaries. We expect to follow a similar process
when establishing area designations for any new or
revised PM2.5 NAAQS.
183 https://www3.epa.gov/pmdesignations/
2012standards/docs/april2013guidance.pdf.
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consider in identifying appropriate
designations for areas and boundaries,
among other relevant topics. For
informational purposes, the public can
comment on the process and schedule
for the initial area designations and
nonattainment boundary setting effort
associated with a new or revised PM2.5
NAAQS. As noted above, the EPA does
not expect to respond to these
comments in the final regulatory action
establishing the NAAQS.
As in past iterations of the PM2.5
NAAQS, the EPA intends to make the
designations for any revised NAAQS
based on the most recent 3 years of
complete and valid air quality data.
Accordingly, the EPA recommends that
states base their initial designation
recommendations on the most current
available 3 years of complete and valid
air quality data. The EPA intends to use
available air quality data from the
current PM2.5 mass and speciation
monitoring networks and other
technical information. The EPA will
then base the final designations on 3
consecutive years of certified air quality
monitoring data, likely 2021–2023.184
In some areas, State or Tribal air
agencies may have flagged air quality
data for certain days in the Air Quality
System due to potential impacts from
exceptional events (i.e., such as
wildfires or high wind dust storms). Air
quality concentrations on such days
may affect the calculation of design
values for regulatory air monitoring sites
in determining whether such sites may
violate the revised PM2.5 NAAQS, and
therefore could influence the initial area
designations for this revised NAAQS.
Under the 2016 Exceptional Events Rule
(see ‘‘Treatment of Data Influenced by
Exceptional Events; Final Rule,’’ 81 FR
68216, October 3, 2016), an air agency
may submit to the EPA a demonstration
with supporting information and
analyses for each monitor and day the
air agency claims should be excluded
from design value calculations for
regulatory purposes. The EPA has
provided a number of tools to assist air
agencies in preparing their
demonstrations 185 and will continue to
work with air agencies as they identify,
prepare and submit exceptional events
demonstrations. The EPA recognizes
that some areas and stakeholders may be
184 In certain circumstances in which the
Administrator has insufficient information to
promulgate area designations within 2 years from
the promulgation of a new or revised NAAQS, CAA
section 107(d)(1)(B)(i) provides the EPA may extend
the designations schedule by up to 1 year.
185 See EPA’s Exceptional Events homepage at
https://www.epa.gov/air-quality-analysis/treatmentair-quality-data-influenced-exceptional-eventshomepage-exceptional.
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concerned about wildfire and prescribed
fire related impacts to designations and/
or other forthcoming actions of
regulatory significance for which a state
may want to submit an exceptional
events demonstration. The EPA has
already issued guidance addressing
development of exceptional events
demonstrations for both wildfire and
prescribed fires on wildland. Existing
guidance and other tools are available
on the EPA’s website identified above.
The air agency is required to follow the
exceptional events demonstration
submission deadlines that are identified
in Table 2 to 40 CFR 50.14(c)(2)(vi)—
‘‘Schedule for Initial Notification and
Demonstration Submission for Data
Influenced by Exceptional Events for
Use in Initial Area Designations.’’
Further, the EPA has notified states of
areas subject to mitigation plan
provisions. Within 2 years of the
notification, if the air agency has not
submitted a required mitigation plan,
the EPA will not concur with the air
agency’s request to exclude data until
the required plan is submitted and
verified.
As noted earlier, the EPA intends to
provide designation guidance to the
states and tribes around the time of the
promulgation of a revised NAAQS, to
assist in formulating these
recommendations. With regard to the
area designations process, if, after
evaluating the state recommendations in
light of the technical factors, the
Administrator intends to modify any
state area recommendation, the EPA
will notify the appropriate state
Governor no later than 120 days prior to
making final designations decisions. A
state that believes the Administrator’s
intended modification is inappropriate
will have the opportunity to
demonstrate to the EPA why it believes
its original recommendation (or a
revised recommendation) is more
appropriate before final designations are
promulgated. The Administrator will
take any additional input from the state
into account in making final designation
decisions. If the Administrator departs
from the stated intentions in the initial
120-day notification letter in a way that
does not match the most recently
received recommendation from the
Governor (or tribe) as of the date of the
final designation, the Administrator will
provide an additional 120-day
notification letter notifying the
Governor of such modifications. The
EPA invites preliminary comment on all
aspects of the designation process at this
time, which the Agency will consider in
developing any updated guidance.
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B. Section 110(a)(1) and (2)
Infrastructure SIP Requirements
The CAA directs states to address
basic SIP requirements to implement,
maintain, and enforce the NAAQS.
Under CAA sections 110(a)(1) and (2),
states are required to have state
implementation plans that provide the
necessary air quality management
infrastructure including, among other
things, enforceable emissions
limitations, an ambient monitoring
program, an enforcement program, air
quality modeling capabilities, and
adequate personnel, resources, and legal
authority. After the EPA promulgates a
new or revised NAAQS, states are
required to make a new SIP submission
to establish that they meet the necessary
structural requirements for such new or
revised NAAQS or make changes to do
so. The EPA refers to this type of SIP
submission as an ‘‘infrastructure SIP
submission.’’ Under CAA sections
110(a)(1), all states are required to make
these infrastructure SIP submissions
within 3 years after promulgation of a
new or revised primary standard. While
the CAA authorizes the EPA to set a
shorter time for states to make these SIP
submissions, the EPA does not currently
intend to do so.
Under CAA section 110(a)(1) and (2),
states are required to make SIP
submissions that address a number of
requirements pertaining to
implementation, maintenance, and
enforcement of a new or revised
NAAQS. The specific subsections in
CAA section 110(a)(2) require states to
address a number of requirements, as
applicable: (A) Emissions limits and
other control measures, (B) Ambient air
quality monitoring/data system, (C)
Programs for enforcement of control
measures and for construction or
modification of stationary sources, (D)(i)
Interstate pollution transport; and (D)(ii)
Interstate and international pollution
abatement, (E) Adequate resources and
authority, conflict of interest, and
oversight of local governments and
regional agencies, (F) Stationary source
monitoring and reporting, (G)
Emergency episodes, (H) SIP revisions,
(I) Plan revisions for nonattainment
areas, (J) Consultation with government
officials, public notification, PSD and
visibility protection, (K) Air quality
modeling and submission of modeling
data, (L) Permitting fees, and (M)
Consultation and participation by
affected local entities. These
requirements apply to all SIP
submissions in general, but the EPA has
provided specific guidance to states
concerning its interpretation of these
requirements in the specific context of
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infrastructure SIP submissions for a new
or revised NAAQS (Page, 2013).
The EPA interprets the CAA such that
two elements identified in section
110(a)(2) are not subject to the 3-year
submission deadline of section 110(a)(1)
and thus states are not required to
address them in the context of an
infrastructure SIP submission. The
elements pertain to part D, in title I of
the CAA, which addresses plan
requirements for nonattainment areas.
Therefore, for the reasons explained
below, the following section 110(a)(2)
elements are considered by the EPA to
be outside the scope of infrastructure
SIP actions: (1) the portion of section
110(a)(2)(C), programs for enforcement
of control measures and for construction
or modification of stationary sources
that applies to permit programs
applicable in designated nonattainment
areas, (known as ‘‘nonattainment new
source review’’) under part D; and (2)
section 110(a)(2)(I), which requires a SIP
submission pursuant to part D, in its
entirety. The EPA does not expect states
to address the requirement for a new or
revised NAAQS in the infrastructure SIP
submissions to include regulations or
emissions limits developed specifically
for attaining the relevant standard in
areas designated nonattainment for the
proposed revised PM2.5 NAAQS. States
will be required to submit infrastructure
SIP submissions for a revised PM2.5
NAAQS before they are required to
submit nonattainment plan SIP
submissions to demonstrate attainment
with the same NAAQS. States are
required to submit nonattainment plans
to provide for attainment and
maintenance of a revised PM2.5 NAAQS
within 18 months from the effective
date of nonattainment area designations
as required under CAA section
189(a)(2)(B). The EPA reviews and acts
upon these later SIP submissions
through a separate process. For this
reason, the EPA does not expect states
to address new nonattainment area
emissions controls per section
110(a)(2)(I) in their infrastructure SIP
submissions.
One of the required infrastructure SIP
elements is that each state’s SIP must
contain adequate provisions to prohibit,
consistent with the provisions of title I
of the CAA, emissions from within the
state that will significantly contribute to
nonattainment in, or interfere with
maintenance by, any other state of the
primary or secondary NAAQS.186 This
element is often referred to as the ‘‘good
neighbor’’ or ‘‘interstate transport’’
186 CAA
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provision.187 The provision has two
prongs: significant contribution to
nonattainment (prong 1) and
interference with maintenance (prong
2). The EPA and states must give
independent significance to prong 1 and
prong 2 when evaluating downwind air
quality problems under CAA section
110(a)(2)(D)(i)(I).188 Further, case law
has established that the EPA and states
must implement requirements to meet
interstate transport obligations in
alignment with the applicable statutory
attainment schedule of the downwind
areas impacted by upwind-state
emissions.189 Thus, the EPA anticipates
that states will need to address
interstate transport obligations
associated with any revised PM
NAAQS, if finalized, in alignment with
the provisions of subpart 4 of part D of
the CAA, as discussed in more detail in
section VIII.C below. Specifically, states
must implement any measures required
to address interstate transport
obligations as expeditiously as
practicable and no later than the next
statutory attainment date, i.e., for this
NAAQS revision, if finalized, as
expeditiously as practicable but no later
than the end of the sixth calendar year
following nonattainment area
designations. See CAA section 188(c).
The EPA anticipates developing
further information and coordinating
with states with respect to the
requirements of CAA section
110(a)(2)(D)(i)(I) for implementation of
any revised PM NAAQS. We note that
states may elect to make SIP
submissions that address certain
infrastructure SIP elements separately
from the others. In recent years, due in
part to the complexity of addressing
interstate transport obligations, some
states have found it efficient to make
SIP submissions to address the
interstate transport provisions
separately from other infrastructure SIP
elements.
It is the responsibility of each state to
review its air quality management
program’s existing SIP provisions in
light of each new or revised NAAQS to
determine if any revisions are necessary
to implement a new or revised NAAQS.
Most states have revised and updated
their SIPs in recent years to address
requirements associated with other
revised NAAQS. For some states, it may
187 CAA section 110(a)(2)(D)(i)(II) also addresses
certain interstate effects that states must address
and thus is also sometimes referred to as relating
to ‘‘interstate transport.’’
188 See North Carolina v. EPA, 531 F.3d 896, 909–
11 (D.C. Cir. 2008).
189 See id. 911–13. See also Wisconsin v. EPA,
938 F.3d 303, 313–20 (D.C. Cir. 2019); Maryland v.
EPA, 958 F.3d 1185, 1203–04 (D.C. Cir. 2020).
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be the case that for a number of
infrastructure elements, the state may
believe it already has adequate state
regulations already adopted and
approved into the SIP to address a
particular requirement with respect to
any revised PM2.5 NAAQS. For such
portions of the state’s infrastructure SIP
submission, the state may provide an
explanation of how its existing SIP
provisions are adequate.
If a state determines that existing SIPapproved provisions are adequate in
light of the revised PM2.5 NAAQS with
respect to a given infrastructure SIP
element (or sub-element), then the state
may make a SIP submission ‘‘certifying’’
that the existing SIP contains provisions
that address those requirements of the
specific section 110(a)(2) infrastructure
elements.190 In the case of such a
certification submission, the state does
not have to include a copy of the
relevant provision (e.g., rule or statute)
itself. Rather, the state in its
infrastructure SIP submission may
provide citations to the SIP-approved
state statutes, regulations, or nonregulatory measures, as appropriate,
which meet the relevant CAA
requirement. Like any other SIP
submission, that state can make such a
certification only after it has provided
reasonable notice and opportunity for
public hearing. This ‘‘reasonable notice
and opportunity for public hearing’’
requirement for infrastructure SIP
submissions is to meet the requirements
of CAA sections 110(a) and 110(l).
Under the EPA’s regulations at 40 CFR
part 51, if a public hearing is held, an
infrastructure SIP submittal must
include a certification by the state that
the public hearing was held in
accordance with the EPA’s procedural
requirements for public hearings. See 40
CFR part 51, appendix V, section 2.1(g),
and see 40 CFR 51.102.
In consultation with its EPA Regional
office, a state should follow all
applicable EPA regulations governing
infrastructure SIP submissions in 40
CFR part 51—e.g., subpart I (Review of
New Sources and Modifications),
subpart J (Ambient Air Quality
Surveillance), subpart K (Source
Surveillance), subpart L (Legal
Authority), subpart M
(Intergovernmental Consultation),
subpart O (Miscellaneous Plan Content
Requirements), subpart P (Protection of
Visibility), and subpart Q (Reports). For
the EPA’s general criteria for
infrastructure SIP submissions, refer to
40 CFR part 51, appendix V, Criteria for
190 A ‘‘certification’’ approach would not be
appropriate for the interstate pollution control
requirements of CAA section 110(a)(2)(D)(i).
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5683
Determining the Completeness of Plan
Submissions. The EPA recommends that
states electronically submit their
infrastructure SIPs to the EPA through
the State Plan Electronic Collaboration
System (SPeCS),191 an online system
available through the EPA’s Central Data
Exchange.
C. Implementing Any Revised PM2.5
NAAQS in Nonattainment Areas
Part D of the CAA describes the
various program requirements that
apply to nonattainment areas for
different NAAQS. Section 172 (found in
subpart 1 of part D) includes general SIP
requirements, and sections 188–190
(found in subpart 4 of part D) include
SIP requirements that specifically
govern implementation for the PM10 and
PM2.5 NAAQS. All PM2.5 nonattainment
areas are initially classified as Moderate
per CAA section 188(a). Under section
189(a)(2), states are required to submit
attainment plan SIP submissions to the
EPA within 18 months of the effective
date of area designations. These plans
need to show how the nonattainment
area will attain the primary PM2.5
standards ‘‘as expeditiously as
practicable,’’ but presumptively by no
later than the end of the 6th calendar
year after the effective date of
designations. For example, if the EPA
finalizes nonattainment designations for
a revised PM2.5 NAAQS in 2024, then
the outermost statutory Moderate area
attainment date would be December 31,
2030. If the state fails to attain the
standard by the end of the 6th calendar
year after the effective date of
designations, the EPA is required to
reclassify the area to Serious, and the
state then must attain the standard by
the end of the 10th calendar year after
the effective date of designations (e.g.,
December 31, 2034).
On August 24, 2016, the EPA issued
a detailed SIP Requirements Rule for
implementing the PM2.5 NAAQS (81 FR
58010, August 24, 2016) (PM2.5 SIP
Requirements Rule). It provides
guidance and establishes additional
regulatory requirements for states
regarding development of attainment
plans for nonattainment areas for the
1997, 2006, and 2012 revisions of the
PM2.5 NAAQS. The EPA also intended
this implementation rule to apply to
nonattainment areas designated
pursuant to any future revisions of the
PM2.5 NAAQS. The rule covers a
number of SIP requirements for
nonattainment areas, including a
nonattainment area emissions
inventory, policies regarding PM2.5
precursor pollutants (i.e., SO2, NOX,
191 https://cdx.epa.gov/.
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VOC, and ammonia), control strategies
(such as reasonably available control
measures and reasonably available
control technology), air quality
modeling, attainment demonstrations,
reasonable further progress
requirements, quantitative milestones,
and contingency measures. Guidance
provided in the PM2.5 SIP Requirements
Rule is supplemented by other EPA
guidance documents, including
guidance on emissions inventory
development (80 FR 8787, February 19,
2015; U.S. EPA, 2017), optional PM2.5
precursor demonstrations (U.S. EPA,
2019b),192 and guidance on air quality
modeling for meeting air quality goals
for the ozone and PM2.5 NAAQS and
regional haze program (U.S. EPA,
2018b).
Under the basic approach outlined in
the PM2.5 SIP Requirements Rule, a state
would first develop an updated
emissions inventory of sources and
emissions activities in the
nonattainment area. It would then use
air quality modeling or other tools to
estimate the air quality improvement
that can be expected in the
nonattainment area by the attainment
year due to enforceable and existing ‘‘on
the books’’ Federal, state, and local
emissions reduction measures. The state
also would work with the regulated
community and other stakeholders to
evaluate potential control measures for
emissions sources and activities in the
nonattainment area, and identify the
additional reasonably available control
measures (RACM) and reasonably
available control technology (RACT)
that can be implemented by these
sources in order to attain the standard
as expeditiously as practicable, but no
later than by the end of the 6th calendar
year after the effective date of
designations.
The evaluation of air quality
improvement associated with potential
future emissions reductions is
commonly performed with
sophisticated air quality modeling tools.
Given that fine particle concentrations
are affected both by regionallytransported pollutants (e.g., SO2 and
NOX emissions from power plants) and
emissions of direct PM2.5 and other
pollutants from local sources in the
nonattainment area (e.g., steel mills, rail
yards, highway mobile sources), the
EPA recommends the use of regional
photochemical models (such as CMAQ
and CAMx), in combination with
192 Provides guidance on developing
demonstrations under section 189(e) intended to
show that a certain PM2.5 precursor in a particular
nonattainment area does not significantly
contribute to PM2.5 concentrations that exceed the
standard.
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source-oriented dispersion models (such
as the American Meteorological Society/
Environmental Protection Agency
Regulatory Model (AERMOD)), as
needed, to develop PM2.5 attainment
strategies for any revised PM2.5 NAAQS.
The EPA SIP modeling guidance
provides details on the development of
attainment demonstrations, and the EPA
will continue to assist air agencies in
modeling and technical analyses (80 FR
8787, February 19, 2015; U.S. EPA,
2017).
The PM2.5 SIP Requirements Rule
provides recommendations to states
regarding when and how to consider
environmental justice in the context of
PM2.5 attainment planning. Some of the
considerations for states include: (1)
identifying areas with overburdened
communities where more ambient
monitoring may be warranted; (2)
targeting emissions reductions that may
be needed to attain the PM2.5 NAAQS;
and (3) increasing opportunities for
meaningful involvement for
overburdened populations (80 FR
58010, 58136, August 25, 2016). The
EPA expects states to consider these and
other factors as part of their SIP
development process.
The PM2.5 SIP Requirements Rule
outlines some examples of how states
can implement these
recommendations.193 For instance,
states can use modeling and screening
tools to better understand where sources
of PM2.5 or PM2.5 precursor emissions
are located and identify areas that may
be candidates for additional ambient
monitoring. Furthermore, once these
target areas are identified, states can
prioritize direct PM2.5 or PM2.5
precursor control measures and
enforcement strategies in these areas to
reduce ambient PM2.5 and achieve the
NAAQS. The EPA recognizes that states
have flexibility under the CAA to
concentrate state resources on
controlling sources of PM2.5 emissions
that directly and adversely affect certain
populations currently experiencing
disparities in PM2.5 exposures and
PM2.5-related health risk, thereby
maximizing health benefits for those
populations. Moreover, states can
establish opportunities to bolster
meaningful involvement in a number of
ways, such as communicating with
communities with disparities in
exposures and risks in appropriate
languages and developing enhanced
notice-and-comment opportunities for
those communities.
193 For more information on the EPA’s
recommendations and examples, see 81 FR 58010,
58137, August 24, 2016.
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As previously mentioned, the 2016
PM2.5 SIP Requirements Rule is
structured in such a way that it provides
guidance and regulatory requirements
for remaining nonattainment areas for
the 1997, 2006, and 2012 revisions of
the PM2.5 NAAQS, as well as for
nonattainment areas designated
pursuant to any future revisions of the
PM2.5 NAAQS. Thus, the EPA is not
proposing changes to the current PM2.5
SIP Requirements Rule in this proposed
rulemaking, and therefore is not
requesting comment on that rule.
D. Implementing the Primary and
Secondary PM10 NAAQS
As summarized in sections III.C.3 and
III.D.3 above, the EPA is proposing to
retain the current primary and
secondary 24-hour PM10 standards to
protect against the health effects
associated with short-term exposures to
thoracic coarse particles and against the
welfare effects considered in this
reconsideration (i.e., visibility, climate,
and materials effects). The EPA intends
to retain the existing implementation
strategy for meeting the CAA
requirements for the PM10 NAAQS.
States and emissions sources should
continue to follow the existing guidance
and regulations for implementing the
current standards.
E. Prevention of Significant
Deterioration and Nonattainment New
Source Review Programs for the
Proposed Revised Primary Annual PM2.5
NAAQS
The CAA, at parts C and D of title I,
contains preconstruction review and
permitting programs applicable to new
major stationary sources and major
modifications of existing major sources.
The preconstruction review of each new
major stationary source and major
modification applies on a pollutantspecific basis, and the requirements that
apply for each pollutant depend on
whether the area in which the source is
situated is designated as attainment (or
unclassifiable) or nonattainment for that
pollutant. In areas designated
attainment or unclassifiable for a
pollutant, the Prevention of Significant
Deterioration (PSD) requirements under
part C apply to construction at major
sources. In areas designated
nonattainment for a pollutant, the
Nonattainment New Source Review
(NNSR) requirements under part D
apply to major source construction.
Collectively, those two sets of permit
requirements are commonly referred to
as the ‘‘major New Source Review’’ or
‘‘major NSR’’ programs.
Until the EPA designates an area with
respect to the proposed revised PM2.5
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NAAQS, the NSR provisions applicable
under an area’s designation for the 1997,
2006, and 2012 PM2.5 NAAQS would
continue to apply. See 40 CFR
51.166(i)(2) and 52.21(i)(2). That is, for
areas designated as attainment/
unclassifiable for the 1997, 2006, and
2012 PM2.5 NAAQS, PSD will apply to
new major stationary sources and major
modifications that trigger major source
permitting requirements for PM2.5. For
areas designated nonattainment for the
1997, 2006, or 2012 PM2.5 NAAQS,
NNSR requirements will apply for new
major stationary sources and major
modifications that trigger major source
permitting requirements for PM2.5.
When the new designations for the
proposed revised PM2.5 NAAQS, if
finalized, become effective, those
designations will further inform
whether PSD or NNSR applies to PM2.5
in a particular area. New major sources
and major modifications will be subject
to the PSD program requirements for
PM2.5 if they are located in an area that
does not have a current nonattainment
designation under CAA section 107 for
PM2.5.194
The EPA has assessed the proposed
revision of the level of the primary
annual PM2.5 NAAQS and is not
proposing any changes to the NSR
program regulations as part of this
proposal to revise the PM2.5 NAAQS.
Sources and reviewing authorities will
be able to use existing NSR regulatory
provisions. Under the PSD program, the
applicant must demonstrate that the
new or modified source emissions
increase does not cause or contribute to
a NAAQS violation. In 2017, the EPA
revised the Guideline on Air Quality
Models (published as appendix W to 40
CFR part 41) to address primary and
secondary PM2.5 impacts in making this
demonstration and has since provided
associated technical guidance, models
and tools, such as the recent ‘‘Final
Guidance for Ozone and Fine
Particulate Matter Permit Modeling’’
(July 29, 2022).195 The EPA will
194 40
CFR 51.166(i)(2) and 52.21(i)(2)
July 29, 2022, the EPA issued ‘‘Final
Guidance for Ozone and Fine Particulate Matter
Permit Modeling,’’ available at https://
www.epa.gov/system/files/documents/2022-07/
Guidance_for_O3_PM25_Permit_Modeling.pdf. This
guidance provides the EPA’s recommendations for
how a stationary source seeking a PSD permit may
demonstrate that it will not cause or contribute to
a violation of the National Ambient Air Quality
Standards for Ozone and PM2.5 and PSD increments
for PM2.5, as required under section 165(a)(3) of the
Clean Air Act and 40 CFR 51.166(k) and 52.21(k).
The EPA has also previously issued two technical
guidance documents for use in conducting these
demonstrations: ‘‘Guidance on the Development of
Modeled Emission Rates for Precursors (MERPs) as
a Tier 1 Demonstration Tool for Ozone and PM2.5
under the PSD Permitting Program,’’ available at
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consider whether changes or updates to
PSD program guidance or associated
tools are warranted as a result of the
proposed revision to the primary annual
PM2.5 NAAQS, should it be finalized,
and would communicate such changes
through separate action(s) following
promulgation of a revised standard.
The statutory requirements for a PSD
permit program set forth under part C of
title I of the CAA (sections 160 through
169) are addressed by the EPA’s PSD
regulations found at 40 CFR 51.166
(minimum requirements for an
approvable PSD SIP) and 40 CFR 52.21
(PSD permitting program for permits
issued under the EPA’s Federal
permitting authority). These regulations
already apply for PM2.5 in areas that
have been designated attainment or
unclassifiable for PM2.5 whenever a
proposed new major source or major
modification triggers PSD requirements
for PM2.5.
For PSD, a ‘‘major stationary source’’
is one with the potential to emit 250
tons per year (tpy) or more of any
regulated NSR pollutant, unless the new
or modified source is classified under a
list of 28 source categories contained in
the statutory definition of ‘‘major
emitting facility’’ in section 169(1) of
the CAA. For those 28 source categories,
a ‘‘major stationary source’’ is one with
the potential to emit 100 tpy or more of
any regulated NSR pollutant. A ‘‘major
modification’’ is a physical change or a
change in the method of operation of an
existing major stationary source that
results, first, in a significant emissions
increase of a regulated NSR pollutant
and, second, in a significant net
emissions increase of that pollutant. See
40 CFR 51.166(b)(2)(i), 40 CFR
52.21(b)(2)(i). The EPA PSD regulations
define the term ‘‘regulated NSR
pollutant’’ to include any pollutant for
which a NAAQS has been promulgated
and any pollutant identified in the EPA
regulations as a constituent or precursor
to such pollutant. See 40 CFR
51.166(b)(49), 40 CFR 52.21(b)(50).
These regulations identify SO2 and NOX
as precursors to PM2.5 in all attainment
and unclassifiable areas. See 40 CFR
51.166(b)(49)(i), 40 CFR 52.21(b)(50)(i).
Thus, for PM2.5, the PSD program
currently requires the review and
control of emissions of direct PM2.5
emissions and SO2 and NOX (as
https://www.epa.gov/sites/default/files/2020-09/
documents/epa-454_r-19-003.pdf, and ‘‘Guidance
on the Use of Models for Assessing the Impacts of
Emissions from Single Sources on the Secondarily
Formed Pollutants: Ozone and PM2.5,’’ available at
https://www.epa.gov/sites/default/files/2020-09/
documents/epa-454_r-16-005.pdf.
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precursors to PM2.5), as applicable.196
Among other things, for each regulated
NSR pollutant emitted or increased in a
significant amount, the PSD program
requires a new major stationary source
or a major modification to apply the
‘‘best available control technology’’
(BACT) and to conduct an air quality
impact analysis to demonstrate that the
proposed major stationary source or
major modification will not cause or
contribute to a violation of any NAAQS
or PSD increment.197 See CAA section
165(a)(3) and (4), 40 CFR 51.166(j) and
(k), 40 CFR 52.21(j) and (k). The PSD
requirements may also include, in
appropriate cases, an analysis of
potential adverse impacts on Class I
areas. See CAA sections 162(a) and 165,
40 CFR 51.166(p); 40 CFR 52.21(p)).198
The EPA has developed the Guideline
on Air Quality Models and other
documents to, among other things,
provide methods and guidance for
demonstrating compliance with the
PM2.5 NAAQS and PSD increments for
PM2.5.199
The EPA has historically interpreted
the requirement for an air quality
impact analysis under CAA section
165(a)(3) and the implementing
regulations to include a requirement to
demonstrate that emissions from the
proposed facility will not cause or
contribute to a violation of any NAAQS
196 Sulfur dioxide is a precursor to PM
2.5 in all
attainment and unclassifiable areas. NOX is
presumed to be a precursor to PM2.5 in all
attainment and unclassifiable areas, unless a state
or the EPA demonstrates that emissions of NOX
from sources in a specific area are not a significant
contributor to that area’s ambient PM2.5
concentrations. VOC is presumed not to be a
precursor to PM2.5 in any attainment or
unclassifiable area, unless a state or the EPA
demonstrates that emissions of VOC from sources
in a specific area are a significant contributor to that
area’s ambient PM2.5 concentrations.
197 By establishing the maximum allowable level
of ambient pollutant concentration increase in a
particular area, an increment defines ‘‘significant
deterioration’’ of air quality in that area. Increments
are defined by the CAA as maximum allowable
increases in ambient air concentrations above a
baseline concentration and are specified in the PSD
regulations by pollutant and area classification
(Class I, II and III). 40 CFR 51.166(c), 40 CFR
52.21(c); 75 FR 64864; October 20, 2010.
198 Congress established certain Class I areas in
section 162(a) of the CAA, including international
parks, national wilderness areas, and national parks
that meet certain criteria. Such Class I areas, known
as mandatory Federal Class I areas, are afforded
special protection under the CAA. In addition,
States and Tribal governments may establish Class
I areas within their own political jurisdictions to
provide similar special air quality protection.
199 See 40 CFR part 51, appendix W; 82 FR 5182,
January 17, 2017; See also U.S. EPA, 2021c. The
EPA provided an initial version of the same
guidance for public comment on February 10, 2020.
Upon consideration of the comments received, and
consistent with Executive Order 13990, the EPA
revised the initial draft guidance and posted the
revised version for additional public comment.
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that is in effect as of the date a PSD
permit is issued, except to the extent
that a pending permit application was
subject to grandfathering provisions that
the EPA had established through
rulemaking. The EPA is not proposing
such provisions for this action. In past
NAAQS revision rules, including the
2012 PM2.5 NAAQS (78 FR 3086,
January 15, 2013) and 2015 Ozone
NAAQS (80 FR 65292, October 26,
2015), the EPA included limited
grandfathering provisions that exempted
certain pending PSD permit actions
(those that had reached a particular
stage in the permitting process at the
time the revised NAAQS was
promulgated or became effective) from
the requirement to demonstrate that the
proposed emissions increases would not
cause or contribute to a violation of the
revised NAAQS. In August 2019, the
U.S. Court of Appeals for the D.C.
Circuit vacated the grandfathering
provision in the PSD rules applicable to
the 2015 Ozone NAAQS, finding that
the provision contradicted ‘‘Congress’s
‘express policy choice’ not to allow
construction which will ‘cause or
contribute to’ nonattainment of ‘any’
effective NAAQS, regardless of when
they are adopted or when a permit was
completed.’’ Murray Energy Corp. v.
EPA, 936 F.3d 597, 627 (D.C. Cir.
2019).200 Based on that court decision,
the EPA is not proposing any
grandfathering provision for this
proposed PM2.5 NAAQS revision, if
finalized. Accordingly, PSD permits
issued on or after the effective date of
any final revised PM2.5 NAAQS would
require a demonstration that the
proposed emissions increases would not
cause or contribute to a violation of the
revised PM2.5 NAAQS.
The EPA anticipates that, if this rule
is finalized as proposed, the existing
PM2.5 air quality in some areas will not
be in attainment of the new revised
primary annual PM2.5 NAAQS, and that
these areas will be designated as
‘‘nonattainment’’ at a later date,
consistent with the designation process
described in the preceding sections.
However, until such nonattainment
designation occurs, proposed new major
sources and major modifications located
in any area currently designated
attainment or unclassifiable for PM2.5
will continue to be subject to the PSD
program requirements for PM2.5.201 This
200 While
the specifics of this case involved the
2015 ozone NAAQS, the case was based upon an
interpretation of CAA section 165(a) and therefore
applies equally to any PSD grandfathering for a new
or revised NAAQS.
201 Any proposed major stationary source or
major modification triggering PSD requirements for
PM2.5 that does not receive its PSD permit by the
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raises the question as to how a source
can be issued a PSD permit in light of
known existing ambient violations of
the revised NAAQS. Section
165(a)(3)(B) of the CAA states that a
proposed source may not construct
unless it demonstrates that it will not
cause or contribute to a violation of any
NAAQS. This statutory requirement is
implemented through a provision
contained in the PSD regulations at 40
CFR 51.166(k) and 52.21(k).202 If a
source cannot make this demonstration,
or if its initial air quality impact
analysis shows that the source’s impact
would cause or contribute to a violation,
a PSD permit may not be issued unless
the permit applicant compensates for
the adverse impact that would
otherwise cause or contribute to a
violation of the NAAQS. While the PSD
regulations do not explicitly specify
remedial actions that a prospective
source can take to address such a
situation, the EPA has historically
recognized in regulations, and through
other actions, that sources applying for
PSD permits may utilize offsets as part
of the required PSD demonstration
under CAA section 165(a)(3)(B).203
Part D of title I of the CAA includes
preconstruction review and permitting
requirements applicable to new major
stationary sources and major
modifications located in areas
designated nonattainment for a
pollutant for which a NAAQS has been
established (i.e., a criteria pollutant).
The relevant part D requirements are
typically referred to as the NNSR
program. The EPA’s regulations for the
NNSR programs are contained in 40
CFR 51.165 and 52.24 and part 51,
appendix S. Specifically, the EPA has
effective date of a new nonattainment designation
for the area where the source would locate would
then be required to satisfy applicable NNSR
preconstruction permit requirements for PM2.5.
202 40 CFR 51.166(k) requires that SIPs shall
provide that the owner or operator of the proposed
source or modification shall demonstrate that
allowable emission increases from the proposed
source or modification, in conjunction with all
other applicable emissions increases or reductions
(including secondary emissions), would not cause
or contribute to air pollution in violation of: (i) any
national ambient air quality standard in any air
quality control region; or (ii) any applicable
maximum allowable increase over the baseline
concentration in any area.
203 See, e.g., Page, 2010; 44 FR 3274, 3278,
January 16, 1979; See also In re Interpower of New
York, Inc., 5 E.A.D. 130, 141 (EAB 1994) (describing
an EPA Region 2 PSD permit that relied in part on
offsets to demonstrate the source would not cause
or contribute to a violation of the NAAQS). 52 FR
24634, 24684, July 1, 1987; 78 FR 3085, 3261–62,
Jan. 15, 2013. The EPA has recognized the ability
of sources to obtain offsets in the context of PSD
though the PSD provisions of the Act do not
expressly reference offsets as the NNSR provisions
of the Act do. See 80 FR 65292, 65441, October 26,
2015.
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developed minimum program
requirements for an NNSR program that
is approvable in a SIP, and those
requirements, which include
requirements for PM2.5, are contained in
40 CFR 51.165. In addition, 40 CFR part
51, appendix S, contains requirements
constituting an interim NNSR program.
This program enables NNSR permitting
in nonattainment areas by states that
lack a SIP-approved NNSR permitting
program during the time between the
date of the relevant designation and the
date that the EPA approves into the SIP
a NNSR program. See 40 CFR part 51,
appendix S, section I; 40 CFR 52.24(k).
For NNSR, ‘‘major stationary source’’
is generally defined as a source with the
potential to emit at least 100 tpy of the
regulated NSR pollutant for which the
area is designated nonattainment. In
some cases, however, the CAA and the
NNSR regulations define ‘‘major
stationary source’’ for NNSR in terms of
a lower rate dependent on the pollutant
and degree of nonattainment in the area.
For PM2.5, in addition to the general
threshold level of 100 tpy, a lower major
source threshold of 70 tpy applies in
Serious PM2.5 nonattainment areas
pursuant to subpart 4 of part D, title I
of the CAA. See 40 CFR
51.165(a)(1)(iv)(A)(1)(vii) and (viii); 40
CFR part 51, appendix S, II.A.4.(i)(a)(7)
and (8).
Under the NNSR program, direct
PM2.5 emissions and emissions of each
PM2.5 precursor are reviewed separately
in accordance with the applicable major
source threshold. For example, the
threshold for Serious PM2.5
nonattainment areas is 70 tpy of direct
PM2.5, as well as for the PM2.5
precursors SO2, NOX, VOC, and
ammonia.204 See 40 CFR
51.165(a)(1)(iv)(A)(1)(vii) and (viii); 40
CFR part 51, appendix S, II.A.4.(i)(a)(7)
and (8). For modifications, NNSR
applies to proposed physical changes or
changes in the method of operation of
an existing stationary source where (1)
the source is major for the
nonattainment pollutant (or a precursor
for that pollutant) and (2) the physical
change or change in the method of
operation of a major stationary source
results, first, in a significant emissions
increase of a regulated NSR pollutant
and, second, in a significant net
emissions increase of that same
204 All recognized precursors to PM
2.5 are
regulated as precursors for NNSR. See 40 CFR
51.165(a)(1)(xxxvii)(C)(2). No significant emission
rate is established by the EPA for ammonia, and
states are required to define ‘‘significant’’ for
ammonia for their respective areas unless the state
pursues the optional precursor demonstration to
exclude ammonia from planning requirements. See
40 CFR 51.165(a)(1)(x)(F); 40 CFR 51.165(a)(13).
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nonattainment pollutant (or same
precursor for that pollutant). See 40 CFR
51.165(a)(1)(v)(A); 40 CFR part 51,
appendix S, II.A.5.(i).
For example, to qualify as a major
modification for SO2 (as a PM2.5
precursor) in a moderate PM2.5
nonattainment area, the existing source
would have to have the potential to emit
100 tpy or more of SO2, and the project
would have to result in an increase in
SO2 emissions of 40 tpy or more. See 40
CFR 51.165(a)(1)(x)(A). New major
stationary sources and major
modifications for PM2.5 subject to NNSR
must comply with the ‘‘lowest
achievable emission rate’’ (LAER) as
defined in the CAA and NNSR rules, as
well as performing other analyses as
required under section 173 of the CAA.
Following the promulgation of any
revised NAAQS for PM2.5, some new
nonattainment areas for PM2.5 may
result. Where a state does not have an
NNSR program or where the current
NNSR program does not apply to PM2.5,
that state will be required to submit the
necessary SIP revisions to ensure that
new major stationary sources and major
modifications for PM2.5 undergo
preconstruction review pursuant to the
NNSR program. States are required to
submit nonattainment plans to provide
for attainment and maintenance of a
revised PM2.5 NAAQS within 18 months
from the effective date of nonattainment
area designations as required under
CAA section 189(a)(2)(B). Therefore,
states whose existing NNSR program
requirements, if any, cannot be
interpreted to apply to the revised
primary annual PM2.5 NAAQS at that
time will be allowed to issue the
necessary permits in accordance with
the applicable nonattainment permitting
requirements contained in 40 CFR part
51, appendix S, which would apply to
the revised PM2.5 NAAQS upon its
effective date. See 73 FR 28321, 28340,
May 16, 2008.
Finally, the EPA recommends that,
where appropriate, PSD and NNSR
permitting authorities assess impacts to
communities with environmental justice
concerns. For example, this may include
conducting a demographic analysis to
inform development of a plan for
community outreach and engagement,
conducting a cumulative emissions
impact analysis,205 or considering the
environmental and social costs imposed
205 The permitting authority may conduct a
cumulative analysis of the projected PM2.5
emissions from all emission units at the proposed
facility and PM2.5 emissions from nearby facilities,
to provide a more complete assessment of the
ambient air impacts of the proposed facility on
affected communities. See 40 CFR part 51,
appendix W, section 9.2.3.
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on the impacted community when
conducting an alternative sites
analysis.206 Another option could be
improving the understanding of the
potential impact of minor sources by
generating an emissions inventory for
such minor sources, including sources
that are not currently required to report
emissions, to generate options on how
emissions can be reduced in the target
area. See 81 FR 58010, 58137. The EPA
anticipates developing further
information and consulting with
permitting authorities on how to best
address environmental justice in the
permitting process.
F. Transportation Conformity Program
Transportation conformity is required
under CAA section 176(c) to ensure that
transportation plans, transportation
improvement programs (TIPs) and
federally supported highway and transit
projects will not cause or contribute to
any new air quality violation, increase
the frequency or severity of any existing
violation, or delay timely attainment or
any required interim emissions
reductions or other milestones.
Transportation conformity applies to
areas that are designated as
nonattainment or nonattainment areas
that have been redesignated to
attainment with an approved CAA
section 175A maintenance plan (i.e.,
maintenance areas) for transportationrelated criteria pollutants: carbon
monoxide, ozone, NO2, PM2.5, and PM10.
Transportation conformity for any new
or revised NAAQS for PM2.5 does not
apply until one year after the effective
date of the nonattainment designation
for that NAAQS. See CAA section
176(c)(6) and 40 CFR 93.102(d)). The
EPA’s Transportation Conformity
Rule 207 establishes the criteria and
procedures for determining whether
transportation activities conform to the
SIP. The EPA is not proposing changes
to the transportation conformity rule in
this proposed rulemaking. The EPA
notes that the transportation conformity
rule already addresses the PM2.5 and
PM10 NAAQS. However, in the future,
the EPA will review the need to issue
or revise guidance describing how the
current conformity rule applies in
nonattainment and maintenance areas
206 Section 173(a)(5) of the CAA requires for an
NNSR permit ‘‘an analysis of alternative sites, sizes,
production processes, and environmental control
techniques for such proposed source [that]
demonstrates that benefits of the proposed source
significantly outweigh the environmental and social
costs imposed as a result of its location,
construction, or modification.’’ This requirement is
referred to as the ‘‘alternative sites analysis.’’
207 40 CFR part 93, subpart A
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for any new or revised primary or
secondary PM NAAQS, as needed.
G. General Conformity Program
The general conformity program
implements CAA section 176(c) and
requires that Federal agencies do not
adopt, accept, approve, or fund
activities that are not consistent with
state air quality goals. General
conformity applies to any Federal action
(e.g., funding, licensing, permitting, or
approving) if (1) the action takes place
in a nonattainment or maintenance area
for any of the criteria pollutants and (2)
it is not a Federal Highway
Administration (FHWA) or Federal
Transit Administration (FTA) project as
defined in 40 CFR 93.101 (these projects
are covered under the transportation
conformity program described above).
The EPA’s General Conformity
Rule 208 establishes the criteria and
procedures for determining if a Federal
action conforms to the applicable
attainment plan. General conformity for
any revised PM2.5 NAAQS does not
apply until one year after the effective
date of the nonattainment designation
for that NAAQS. The EPA is not
proposing changes to the General
Conformity Rule in this proposed
rulemaking. The EPA notes that the
General Conformity Rule already
addresses the PM2.5 and PM10 NAAQS.
IX. Statutory and Executive Order
Reviews
Additional information about these
statutes and Executive orders can be
found at https://www.epa.gov/lawsregulations/laws-and-executive-orders.
A. Executive Order 12866: Regulatory
Planning and Review and Executive
Order 13563: Improving Regulation and
Regulatory Review
This action is an economically
significant regulatory action that was
submitted to the Office of Management
and Budget (OMB) for review. Any
changes made in response to OMB
recommendations have been
documented in the docket. The EPA
prepared an illustrative analysis of the
potential costs and benefits associated
with this action. This analysis is
contained in the document ‘‘Regulatory
Impact Analysis for the Proposed
Reconsideration of the National
Ambient Air Quality Standards for
Particulate Matter,’’ which is available
in the Regulatory Impact Analysis (RIA)
docket (EPA–HQ–OAR–2019–0587) and
briefly summarized below. The RIA
estimates the costs and monetized
human health benefits in 2032, after
208 40
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implementing existing and expected
regulations and assessing emissions
reductions to meet the current annual
and 24-hour particulate matter NAAQS
(12/35 mg/m3), associated with applying
national control strategies for the
proposed annual and 24-hour
alternative standard levels of 10/35 mg/
m3 and 9/35 mg/m3, as well as the
following two more stringent alternative
standard levels: (1) an alternative
annual standard level of 8 mg/m3 in
combination with the current 24-hour
standard (i.e., 8/35 mg/m3), and (2) an
alternative 24-hour standard level of 30
mg/m3 in combination with the
proposed annual standard level of 10
mg/m3 (i.e., 10/30 mg/m3). Table 2
provides a summary of the estimated
monetized benefits, costs, and net
benefits associated with applying
national control strategies toward
reaching alternative standard levels.
However, the CAA and judicial
decisions make clear that the economic
and technical feasibility of attaining
ambient standards are not to be
considered in setting or revising
NAAQS, although such factors may be
considered in the development of state
plans to implement the standards.
Accordingly, although an RIA has been
prepared, the results of the RIA have not
been considered in issuing this
proposed rule.
TABLE 2—ESTIMATED MONETIZED BENEFITS, COSTS, AND NET BENEFITS OF THE ILLUSTRATIVE CONTROL STRATEGIES
APPLIED TOWARD THE PRIMARY ALTERNATIVE ANNUAL AND DAILY STANDARD LEVELS OF 10/35 μg/m3, 10/30 μg/m3,
9/35 μg/m3, AND 8/35 μg/m3 IN 2032 FOR THE U.S.
[Millions of 2017$]
10/35
10/30
9/35
8/35
Benefits a ........................................
Costs b ............................................
$8,500 and $17,000 .......
$95 .................................
$9,600 and $20,000 .......
$260 ...............................
$21,000 and $43,000 .....
$390 ...............................
$46,000 and $95,000
$1,800
Net Benefits ............................
$8,400 and $17,000 .......
$9,300 and $19,000 .......
$20,000 and $43,000 .....
$44,000 and $93,000
Notes: Rows may not appear to add correctly due to rounding. We focus results to provide a snapshot of costs and benefits in 2032, using the
best available information to approximate social costs and social benefits recognizing uncertainties and limitations in those estimates. The estimated costs and monetized human health benefits associated with applying national control strategies do not fully account for all the emissions
reductions needed to reach the proposed and more stringent alternative standard levels for some standard levels analyzed.
a We assume that there is a cessation lag between the change in PM exposures and the total realization of changes in mortality effects. Specifically, we assume that some of the incidences of premature mortality related to PM2.5 exposures occur in a distributed fashion over the 20
years following exposure, which affects the valuation of mortality benefits at different discount rates. Similarly, we assume there is a cessation
lag between the change in PM exposures and both the development and diagnosis of lung cancer. The benefits are associated with two point
estimates from two different epidemiologic studies, and we present the benefits calculated at a real discount rate of 3 percent. The benefits exclude additional health and welfare benefits that could not be quantified.
b The costs are annualized using a 7 percent interest rate.
B. Paperwork Reduction Act (PRA)
This action does not impose an
information collection burden under the
PRA. There are no information
collection requirements directly
associated with a proposed decision to
revise or retain a NAAQS under section
109 of the CAA.
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C. Regulatory Flexibility Act (RFA)
I certify that this action will not have
a significant economic impact on a
substantial number of small entities
under the RFA. This action will not
impose any requirements on small
entities. Rather, this proposed rule
establishes national standards for
allowable concentrations of PM in
ambient air as required by section 109
of the CAA. See also American Trucking
Associations v. EPA, 175 F.3d 1027,
1044–45 (D.C. Cir. 1999) (NAAQS do
not have significant impacts upon small
entities because NAAQS themselves
impose no regulations upon small
entities), rev’d in part on other grounds,
Whitman v. American Trucking
Associations, 531 U.S. 457 (2001).
D. Unfunded Mandates Reform Act
(UMRA)
This action does not contain any
unfunded mandate as described in the
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Unfunded Mandates Reform Act
(UMRA), 2 U.S.C. 1531–1538, and does
not significantly or uniquely affect small
governments. Furthermore, as indicated
previously, in setting a NAAQS the EPA
cannot consider the economic or
technological feasibility of attaining
ambient air quality standards, although
such factors may be considered to a
degree in the development of state plans
to implement the standards. See also
American Trucking Associations v.
EPA, 175 F. 3d at 1043 (noting that
because the EPA is precluded from
considering costs of implementation in
establishing NAAQS, preparation of the
RIA pursuant to the Unfunded
Mandates Reform Act would not furnish
any information that the court could
consider in reviewing the NAAQS).
The EPA acknowledges, however, that
if corresponding revisions to associated
SIP requirements and air quality
surveillance requirements are proposed
at a later time, those revisions might
result in such effects. Any such effects
would be addressed as appropriate if
and when such revisions are proposed.
E. Executive Order 13132: Federalism
This action does not have federalism
implications. It will not have substantial
direct effects on the states, on the
relationship between the National
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Government and the states, or on the
distribution of power and
responsibilities among the various
levels of government. However, the EPA
recognizes that states will have a
substantial interest in this action and
any future revisions to associated
requirements.
F. Executive Order 13175: Consultation
and Coordination With Indian Tribal
Governments
This action does not have Tribal
implications, as specified in Executive
Order 13175. It does not have a
substantial direct effect on one or more
Indian Tribes as tribes are not obligated
to adopt or implement any NAAQS. In
addition, tribes are not obligated to
conduct ambient monitoring for PM or
to adopt the ambient monitoring
requirements of 40 CFR part 58. Thus,
Executive Order 13175 does not apply
to this action. However, consistent with
the EPA Policy on Consultation and
Coordination with Indian Tribes, the
EPA will offer government-togovernment consultation with tribes as
requested.
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G. Executive Order 13045: Protection of
Children From Environmental Health
Risks and Safety Risks
This action is subject to Executive
Order 13045 because it is an
economically significant regulatory
action as defined by Executive Order
12866, and the EPA believes that the
environmental health or safety risk
addressed by this action may have a
disproportionate effect on children. The
Policy on Children’s Health also applies
to this action. Accordingly, we have
evaluated the environmental health or
safety effects of PM exposures on
children. The protection offered by
these standards may be especially
important for children because
childhood represents a lifestage
associated with increased susceptibility
to PM-related health effects. Because
children have been identified as a
susceptible population, we have
carefully evaluated the environmental
health effects of exposure to PM
pollution among children. Children
make up a substantial fraction of the
U.S. population, and often have unique
factors that contribute to their increased
risk of experiencing a health effect due
to exposures to ambient air pollutants
because of their continuous growth and
development. As described in the 2019
Integrated Science Assessment, children
may be particularly at risk for health
effects related to ambient air PM2.5
exposures compared with adults
because they have (1) a developing
respiratory system, (2) increased
ventilation rates relative to body mass
compared with adults, and (3) an
increased proportion of oral breathing,
particularly in boys, relative to adults.
More detailed information on the
evaluation of the scientific evidence and
policy considerations pertaining to
children, including an explanation for
why the Administrator judges the
proposed standards to be requisite to
protect public health, including the
health of children, with an adequate
margin of safety, are contained in
sections II.B and II.D of this preamble.
Copies of all documents have been
placed in the public docket for this
action.
H. Executive Order 13211: Actions
Concerning Regulations That
Significantly Affect Energy Supply,
Distribution or Use
This action is not a ‘‘significant
energy action’’ because it is not likely to
have a significant adverse effect on the
supply, distribution, or use of energy.
The purpose of this action is to propose
to revise the primary annual PM2.5
NAAQS and to retain the primary 24-
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hour PM2.5 NAAQS, primary PM10
NAAQS, and secondary PM NAAQS.
The action does not prescribe specific
pollution control strategies by which
these ambient standards and monitoring
revisions will be met. Such strategies
will be developed by states on a caseby-case basis, and the EPA cannot
predict whether the control options
selected by states will include
regulations on energy suppliers,
distributors, or users. Thus, the EPA
concludes that this proposal does not
constitute a significant energy action as
defined in Executive Order 13211.
I. National Technology Transfer and
Advancement Act (NTTAA)
This action involves technical
standards. The EPA proposes to use the
current indicators for fine (PM2.5) and
coarse (PM10) particles. The indicator
for fine particles is measured using the
Reference Method for the Determination
of Fine Particulate Matter as PM2.5 in the
Atmosphere (appendix L to 40 CFR part
50), which is known as the PM2.5 FRM,
and the indicator for coarse particles is
measured using the Reference Method
for the Determination of Particulate
Matter as PM10 in the Atmosphere
(appendix J to 40 CFR part 50), which
is known as the PM10 FRM.
To the extent feasible, the EPA
employs a Performance-Based
Measurement System (PBMS), which
does not require the use of specific,
prescribed analytic methods. The PBMS
is defined as a set of processes wherein
the data quality needs, mandates or
limitations of a program or project are
specified, and serve as criteria for
selecting appropriate methods to meet
those needs in a cost-effective manner.
It is intended to be more flexible and
cost effective for the regulated
community; it is also intended to
encourage innovation in analytical
technology and improved data quality.
Though the FRM defines the particular
specifications for ambient monitors,
there is some variability with regard to
how monitors measure PM, depending
on the type and size of PM and
environmental conditions. Therefore, it
is not practically possible to fully define
the FRM in performance terms to
account for this variability.
Nevertheless, our approach in the past
has resulted in multiple brands of
monitors being approved as FRM for
PM, and we expect this to continue.
Also, the FRMs described in 40 CFR
part 50 and the equivalency criteria
described in 40 CFR part 53, constitute
a performance-based measurement
system for PM, since methods that meet
the field testing and performance
criteria can be approved as FEMs. Since
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finalized in 2006 (71 FR 61236, October
17, 2006) the new field and performance
criteria for approval of PM2.5 continuous
FEMs has resulted in the approval of 13
approved FEMs. In summary, for
measurement of PM2.5 and PM10, the
EPA relies on both FRMs and FEMs,
with FEMs relying on a PBMS approach
for their approval. The EPA is not
precluding the use of any other method,
whether it constitutes a voluntary
consensus standard or not, as long as it
meets the specified performance
criteria.
J. Executive Order 12898: Federal
Actions To Address Environmental
Justice in Minority Populations and
Low-Income Populations
The EPA believes that this action does
not have disproportionately high and
adverse human health or environmental
effects on minority populations, lowincome populations and/or indigenous
peoples, as specified in Executive Order
12898 (59 FR 7629, February 16, 1994).
The documentation for this assessment
is contained in sections II.B.2, II.C.1,
II.C.3, II.D.2, and II.D. of this preamble
and also in the 2019 Integrated Science
Assessment, Supplement to the 2019
Integrated Science Assessment, and
Policy Assessment. The EPA has
carefully evaluated the potential
impacts on minority populations and
low SES populations as discussed in
sections II.B.2, II.C.1, II.C.3, II.D.2, and
II.D.3 of this preamble. The Integrated
Science Assessment, Supplement to the
Integrated Science Assessment, and
Policy Assessment contain the
evaluation of the scientific evidence,
quantitative risk analyses and policy
considerations that pertain to these
populations. These documents are
available as described in this
SUPPLEMENTARY INFORMATION section and
copies of all documents have been
placed in the public docket for this
action.
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Park, NC. U.S. EPA. EPA–452/R–20–002.
January 2020.
U.S. EPA (2020b). Recommendations for
Nationwide Approval of NafionTM Dryers
Upstream of UV-Absorption Ozone
Analyzers. Office of Air Quality Planning
and Standards, Health and
Environmental Impacts Division.
Research Triangle Park, NC. U.S. EPA.
EPA/600/R–20/390. November 2020.
U.S. EPA (2021a). Supplement to the 2019
Integrated Science Assessment for
Particulate Matter (External Review
Draft). U.S. Environmental Protection
Agency, Office of Research and
Development, Center for Public Health
and Environmental Assessment.
Research Triangle Park, NC. U.S. EPA.
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U.S. EPA (2021b). Comparative Assessment
of the Impacts of Prescribed Fire Versus
Wildfire (CAIF): A Case Study in the
Western U.S. U.S. Environmental
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EPA. EPA/600/R–21/197.
U.S. EPA (2021c). Guidance for Ozone and
Fine Particulate Matter Permit Modeling.
U.S. Environmental Protection Agency,
Office of Air Quality Planning and
Standards, Air Quality Assessment
Division. Research Triangle Park, NC.
U.S. EPA. EPA–454/P–21–001.
September 2021.
U.S. EPA (2022a). Supplement to the 2019
Integrated Science Assessment for
Particulate Matter (Final Report). U.S.
Environmental Protection Agency, Office
of Research and Development, Center for
Public Health and Environmental
Assessment. Research Triangle Park, NC.
U.S. EPA. EPA/600/R 22/028. May 2022.
U.S. EPA (2022b). Policy Assessment for the
Reconsideration of the National Ambient
Air Quality Standards for Particulate
Matter. Office of Air Quality Planning
and Standards, Health and
Environmental Impacts Division.
Research Triangle Park, NC. U.S. EPA.
EPA–452/R–22–004. May 2022.
Urch, B, Speck, M, Corey, P, Wasserstein, D,
Manno, M, Lukic, KZ, Brook, JR, Liu, L,
Coull, B, Schwartz, J, Gold, DR and
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210–218.
Van de Hulst, H (1981). Light scattering by
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van Donkelaar, A, Martin, RV, Li, C and
Burnett, RT (2019). Regional estimates of
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chemical composition of fine particulate
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satellites, models, and monitors.
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Vieira, JL, Guimaraes, GV, de Andre, PA,
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Ward-Caviness, CK, Weaver, AM, Buranosky,
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Schwartz, J, Di, Q, Cascio, WE and DiazSanchez, D (2020). Associations between
long-term fine particulate matter
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Wei, Y, Wang, Y, Di, Q, Choirat, C, Wang, Y,
Koutrakis, P, Zanobetti, A, Dominici, F
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Medicare population: time stratified,
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Research Edition) 367: l6258.
Wei, Y, Yazdi, MD, Di, Q, Requia, WJ,
Dominici, F, Zanobetti, A and Schwartz,
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Environmental Health: A Global Access
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dioxide, sulfur dioxide and carbon
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Wu, X, Braun, D, Schwartz, J,
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Wyatt, LH, Devlin, RB, Rappold, AG, Case,
MW and Diaz-Sanchez, D (2020). Low
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Particle and fibre toxicology 17(1): 1–12.
Yorifuji, T, Kashima, S and Doi, H (2016).
Fine-particulate air pollution from diesel
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Tokyo: a quasi-experimental study.
Epidemiology 27(6): 769–778.
Zhang, H and Kondragunta, S (2021). Daily
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Zhang, Z, Wang, J, Kwong, JC, Burnett, RT,
van Donkelaar, A, Hystad, P, Martin, RV,
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List of Subjects
40 CFR Part 50
Environmental protection, Air
pollution control, Carbon monoxide,
Lead, Nitrogen dioxide, Ozone,
Particulate matter, Sulfur oxides.
40 CFR Part 53
Environmental protection,
Administrative practice and procedure,
Air pollution control, Reporting and
recordkeeping requirements.
Environmental protection,
Administrative practice and procedure,
Air pollution control, Intergovernmental
relations, Reporting and recordkeeping
requirements.
Michael S. Regan,
Administrator.
For the reasons set forth in the
preamble, chapter I of title 40 of the
Code of Federal Regulations is proposed
to be amended as follows:
PART 50—NATIONAL PRIMARY AND
SECONDARY AMBIENT AIR QUALITY
STANDARDS
1. The authority citation for part 50
continues to read as follows:
■
Authority: 42 U.S.C. 7401, et seq.
2. Add § 50.20 to read as follows:
§ 50.20 National primary ambient air
quality standards for PM2.5.
(a) The national primary ambient air
quality standards for PM2.5 are 9.0 to
10.0 micrograms per cubic meter (mg/
m3) annual arithmetic mean
concentration and 35 mg/m3 24-hour
average concentration measured in the
ambient air as PM2.5 (particles with an
aerodynamic diameter less than or equal
to a nominal 2.5 micrometers) by either:
(1) A reference method based on
appendix L to this part and designated
in accordance with part 53 of this
chapter; or
(2) An equivalent method designated
in accordance with part 53 of this
chapter.
(b) The primary annual PM2.5
standard is met when the annual
arithmetic mean concentration, as
determined in accordance with
appendix N to this part, is less than or
equal to 9.0 to 10.0 mg/m3.
(c) The primary 24-hour PM2.5
standard is met when the 98th
percentile 24-hour concentration, as
PO 00000
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Appendix K to Part 50—Interpretation
of the National Ambient Air Quality
Standards for Particulate Matter
1.0
*
40 CFR Part 58
■
determined in accordance with
appendix N to this part, is less than or
equal to 35 mg/m3.
■ 3. Amend appendix K to part 50 as
follows:
■ a. In section 1.0 by revising paragraph
(b);
■ b. In section 2.3 by adding paragraph
(d); and
■ c. In section 3.0 by adding paragraphs
(a) and (b).
The revision and additions read as
follows:
Sfmt 4702
General
*
*
*
*
(b) The terms used in this appendix are
defined as follows:
Average refers to the arithmetic mean of
the estimated number of exceedances per
year, as per section 3.1 of this appendix.
Collocated monitors refer to two or more
air measurement instruments for the same
parameter (e.g., PM10 mass) operated at the
same site location, and whose placement is
consistent with part 53 of this chapter. For
purposes of considering a combined site
record in this appendix, when two or more
monitors are operated at the same site, one
monitor is designated as the ‘‘primary’’
monitor with any additional monitors
designated as ‘‘collocated.’’ It is implicit in
these appendix procedures that the primary
monitor and collocated monitor(s) are all
reference or equivalent methods; however, it
is not a requirement that the primary and
collocated monitors utilize the same specific
sampling and analysis method.
Combined site data record is the data set
used for performing computations in this
appendix and represents data for the primary
monitors augmented with data from
collocated monitors according to the
procedure specified in section 3.0(a) of this
appendix.
Daily value for PM10 refers to the 24-hour
average concentration of PM10 calculated or
measured from midnight to midnight (local
time).
Exceedance means a daily value that is
above the level of the 24-hour standard after
rounding to the nearest 10 mg/m3 (i.e., values
ending in 5 or greater are to be rounded up).
Expected annual value is the number
approached when the annual values from an
increasing number of years are averaged, in
the absence of long-term trends in emissions
or meteorological conditions.
Primary monitors are suitable monitors
designated by a state or local agency in their
annual network plan as the default data
source for creating a combined site data
record. If there is only one suitable monitor
at a particular site location, then it is
presumed to be a primary monitor.
Year refers to a calendar year.
*
2.3
*
*
*
*
*
Data Requirements
*
*
*
*
(d) 24-hour average concentrations will be
computed from submitted hourly PM10
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concentration data for each corresponding
day of the year and the result will be stored
in the first, or start, hour (i.e., midnight, hour
‘0’) of the 24-hour period. A 24-hour average
concentration shall be considered valid if at
least 75 percent of the hourly averages (i.e.,
18 hourly values) for the 24-hour period are
available. In the event that fewer than all 24
hourly average concentrations are available
(i.e., fewer than 24 but at least 18), the 24hour average concentration shall be
computed on the basis of the hours available
using the number of available hours within
the 24-hour period as the divisor (e.g., the
divisor is 19 if 19 hourly values are
available). 24-hour periods with seven or
more missing hours shall also be considered
for computations in this appendix if, after
substituting zero for all missing hourly
concentrations, the resulting 24-hour average
daily value exceeds the level of the 24-hour
standard specified in § 50.6 after rounding to
the nearest 10 mg/m3.
*
*
*
*
*
3.0 Computational Equations for the 24Hour Standards
(a) All computations shown in this
appendix shall be implemented on a sitelevel basis. Site level concentration data shall
be processed as follows:
(1) The default dataset for PM10 mass
concentrations for a site shall consist of the
measured concentrations recorded from the
designated primary monitor(s). All daily
values produced by the primary monitor are
considered part of the site record.
(2) If a daily value is not produced by the
primary monitor for a particular day, but a
value is available from a single collocated
monitor, then that collocated monitor value
shall be considered part of the combined site
data record. If daily value data is available
from two or more collocated monitors, the
average of those collocated values shall be
used as the daily value. The data record
resulting from this procedure is referred to as
the ‘‘combined site data record.’’
(b) In certain circumstances, including but
not limited to site closures or relocations,
data from two nearby sites may be combined
into a single site data record for the purpose
of calculating a valid design value. The
appropriate Regional Administrator may
approve such combinations if the Regional
Administrator determines that the measured
concentrations do not differ substantially
between the two sites, taking into
consideration factors such as distance
between sites, spatial and temporal patterns
in air quality, local emissions and
meteorology, jurisdictional boundaries, and
terrain features.
*
*
*
*
*
4. Amend appendix L to part 50 by
revising section 7.3.4 and adding
section 7.3.4.5 to read as follows:
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■
*
*
*
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*
*
*
*
*
*
*
*
5. Amend appendix N to part 50 as
follows:
■ a. In section 1.0 by revising paragraph
(a); and
■ b. In section 3.0 by adding paragraph
(d)(3); and
■ c. In section 4.1 by revising paragraph
(a); and
■ d. In section 4.2 by revising paragraph
(a).
The addition and revisions read as
follows.
■
Appendix N to Part 50—Interpretation
of the National Ambient Air Quality
Standards for PM2.5
1.0 General
(a) This appendix explains the data
handling conventions and computations
necessary for determining when the national
ambient air quality standards (NAAQS) for
PM2.5 are met, specifically the primary and
secondary annual and 24-hour PM2.5 NAAQS
specified in §§ 50.7, 50.13, 50.18, and 50.20.
PM2.5 is defined, in general terms, as particles
with an aerodynamic diameter less than or
equal to a nominal 2.5 micrometers. PM2.5
mass concentrations are measured in the
ambient air by a Federal Reference Method
(FRM) based on appendix L to this part, as
applicable, and designated in accordance
with part 53 of this chapter or by a Federal
Equivalent Method (FEM) designated in
accordance with part 53 of this chapter. Only
those FRM and FEM measurements that are
derived in accordance with part 58 of this
chapter (i.e., that are deemed ‘‘suitable’’)
shall be used in comparisons with the PM2.5
NAAQS. The data handling and computation
procedures to be used to construct annual
and 24-hour NAAQS metrics from reported
PM2.5 mass concentrations, and the
associated instructions for comparing these
calculated metrics to the levels of the PM2.5
NAAQS, are specified in sections 2.0, 3.0,
and 4.0 of this appendix.
*
*
20:56 Jan 26, 2023
*
7.3.4.5 A second cyclone-type separator
is identified as a Tisch TE–PM2.5C Cyclone
particle size separator specified as part of
EPA-designated reference method RFPS–
1014–219 and as manufactured by Tisch
Environmental Incorporated, 145 S Miami
Avenue, Village of Cleves, Ohio 45002.
*
*
*
*
3.0 Requirements for Data Use and Data
Reporting for Comparisons With the NAAQS
for PM2.5
7.3.4 Particle size separator. The sampler
shall be configured with one of the three
VerDate Sep<11>2014
*
*
Appendix L to Part 50—Reference
Method for the Determination of Fine
Particulate Matter as PM2.5 in the
Atmosphere
*
alternative particle size separators described
in this section. One separator is an impactortype separator (WINS impactor) described in
sections 7.3.4.1, 7.3.4.2, and 7.3.4.3 of this
appendix. One alternative separator is a
cyclone-type separator (VSCCTM) described
in section 7.3.4.4 of this appendix. The other
alternative separator is also a cyclone-type
separator (TE–PM2.5C) described in section
7.3.4.5 of this appendix.
*
*
*
*
(d) * * *
(3) In certain circumstances, including but
not limited to site closures or relocations,
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Sfmt 4702
data from two nearby sites may be combined
into a single site data record for the purpose
of calculating a valid design value. The
appropriate Regional Administrator may
approve such site combinations if the
Regional Administrator determines that the
measured concentrations do not differ
substantially between the two sites, taking
into consideration factors such as distance
between sites, spatial and temporal patterns
in air quality, local emissions and
meteorology, jurisdictional boundaries, and
terrain features.
*
*
*
*
*
4.1 Annual PM2.5 NAAQS
(a) Levels of the primary and secondary
annual PM2.5 National Ambient Air Quality
Standards are specified in §§ 50.7, 50.13,
50.18, and 50.20 as applicable.
*
*
*
*
*
4.2 Twenty-Four-Hour PM2.5 NAAQS
(a) Levels of the primary and secondary 24hour PM2.5 National Ambient Air Quality
Standards are specified in §§ 50.7, 50.13,
50.18, and 50.20 as applicable.
*
*
*
*
*
PART 53—AMBIENT AIR MONITORING
REFERENCE AND EQUIVALENT
METHODS
6. The authority citation for part 53
continues to read as follows:
■
Authority: Sec. 301(a) of the Clean Air Act
(42 U.S.C. sec. 1857g(a)), as amended by sec.
15(c)(2) of Pub. L. 91–604, 84 Stat. 1713,
unless otherwise noted.
Subpart A—General Provisions
7. Amend § 53.4 as follows:
a. By revising paragraph (a);
b. By adding paragraph (b)(7); and
c. By revising paragraph (d).
The revisions and addition read as
follows:
■
■
■
■
§ 53.4 Applications for reference or
equivalent method determinations.
(a) Applications for FRM or FEM
determinations and modification
requests of existing designated
instruments shall be submitted to:
Director, Center for Environmental
Measurement and Modeling, Reference
and Equivalent Methods Designation
Program (MD–205–03), U.S.
Environmental Protection Agency,
Research Triangle Park, North Carolina
27711 (commercial delivery address:
4930 Old Page Road, Durham, North
Carolina 27703).
*
*
*
*
*
(b) * * *
(7) All written materials for new FRM
and FEM applications and modification
requests must be submitted in English
in MS Word format. For any calibration
certificates originally written in a nonEnglish language, the original non-
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English version of the certificate must
be submitted to EPA along with a
version of the certificate translated to
English. All laboratory and field data
associated with new FRM and FEM
applications and modification requests
must be submitted in MS Excel format.
All worksheets in MS Excel must be
unprotected to enable full inspection as
part of the application review process.
*
*
*
*
*
(d) For candidate reference or
equivalent methods or for designated
instruments that are the subject of a
modification request, the applicant, if
requested by EPA, shall provide to EPA
a representative sampler or analyzer for
test purposes. The sampler or analyzer
shall be shipped free on board (FOB)
destination to Director, Center for
Environmental Measurements and
Modeling, Reference and Equivalent
Methods Designation Program (MD
D205–03), U.S. Environmental
Protection Agency, 4930 Old Page Road,
Durham, North Carolina 27703,
scheduled to arrive concurrently with or
within 30 days of the arrival of the other
application materials. This sampler or
analyzer may be subjected to various
tests that EPA determines to be
necessary or appropriate under § 53.5(f),
and such tests may include special tests
not described in this part. If the
instrument submitted under this
paragraph (d) malfunctions, becomes
inoperative, or fails to perform as
represented in the application before the
necessary EPA testing is completed, the
applicant shall be afforded the
opportunity to repair or replace the
device at no cost to the EPA. Upon
completion of EPA testing, the sampler
or analyzer submitted under this
paragraph (d) shall be repacked by EPA
for return shipment to the applicant,
using the same packing materials used
for shipping the instrument to EPA
unless alternative packing is provided
by the applicant. Arrangements for, and
the cost of, return shipment shall be the
responsibility of the applicant. The EPA
does not warrant or assume any liability
for the condition of the sampler or
analyzer upon return to the applicant.
■ 8. Amend § 53.8 by revising paragraph
(a) to read as follows:
§ 53.8 Designation of reference and
equivalent methods.
(a) A candidate method determined
by the Administrator to satisfy the
applicable requirements of this part
shall be designated as an FRM or FEM
(as applicable) by and upon publication
of a notice of the designation in the
Federal Register. Applicants shall not
publicly announce, market, or sell the
candidate sampler and analyzer as an
approved FRM or FEM (as applicable)
until the Federal Register notice has
been published.
*
*
*
*
*
9. Amend § 53.14 by revising
paragraphs (c)(4), (5), and (6) to read as
follows:
■
§ 53.14 Modification of a reference or
equivalent method.
*
*
*
*
*
(c) * * *
(4) Send notice to the applicant that
additional information must be
submitted before a determination can be
made and specify the additional
information that is needed (in such
cases, the 90-day period shall
commence upon receipt of the
additional information).
(5) Send notice to the applicant that
additional tests are necessary and
specify which tests are necessary and
how they shall be interpreted (in such
cases, the 90-day period shall
commence upon receipt of the
additional test data).
(6) Send notice to the applicant that
additional tests will be conducted by
the Administrator and specify the
reasons for and the nature of the
additional tests (in such cases, the 90day period shall commence 1 calendar
day after the additional tests are
completed).
*
*
*
*
*
■ 10. Revise table A–1 to subpart A of
part 53 to read as follows:
TABLE A–1 TO SUBPART A OF PART 53—SUMMARY OF APPLICABLE REQUIREMENTS FOR REFERENCE AND EQUIVALENT
METHODS FOR AIR MONITORING OF CRITERIA POLLUTANTS
Pollutant
SO2 ..............
Reference or equivalent
Reference .............................................
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Equivalent .............................................
CO ...............
Reference .............................................
Equivalent .............................................
O3 ................
Reference .............................................
Equivalent .............................................
NO2 ..............
Reference .............................................
Equivalent .............................................
Pb ................
Reference .............................................
Equivalent .............................................
PM10-Pb ......
Reference .............................................
Equivalent .............................................
PM10 ............
Reference .............................................
Equivalent .............................................
PM2.5 ...........
Reference
Equivalent
Equivalent
Equivalent
Reference
PM10–2.5 .......
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.............................................
Class I .................................
Class II ................................
Class III ...............................
.............................................
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automated
Applicable
appendix of
part 50 of
this chapter
A
B
C
D
E
F
Manual ........
Automated ...
Manual ........
Automated ...
Automated ...
Manual ........
Automated ...
Automated ...
Manual ........
Automated ...
Automated ...
Manual ........
Automated ...
Manual ........
Manual ........
Automated ...
Manual ........
Manual ........
Automated ...
Manual ........
Manual ........
Automated ...
Manual ........
Manual ........
Manual ........
Automated ...
Manual ........
A–2 ........................
A–1 ........................
A–1 ........................
A–1 ........................
C ............................
C ............................
C ............................
D ............................
D ............................
D ............................
F ............................
F ............................
F ............................
G ...........................
G ...........................
G ...........................
Q ...........................
Q ...........................
Q ...........................
J ............................
J ............................
J ............................
L ............................
L ............................
L 1 ..........................
L 1 ..........................
L, O 2 .....................
..........
✓
✓
✓
✓
✓
✓
✓
✓
✓
✓
✓
✓
..........
✓
✓
..........
✓
✓
✓
✓
✓
✓
✓
✓
✓
✓
..........
✓
..........
✓
✓
..........
✓
✓
..........
✓
✓
..........
✓
..........
..........
..........
..........
..........
..........
..........
..........
..........
..........
..........
..........
..........
..........
..........
..........
✓
✓
..........
✓
✓
..........
✓
✓
..........
✓
✓
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✓
✓
..........
✓
✓
..........
✓
✓
..........
✓
✓2
✓
..........
..........
..........
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..........
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..........
..........
..........
..........
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..........
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✓
✓
✓
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✓
✓
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✓
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TABLE A–1 TO SUBPART A OF PART 53—SUMMARY OF APPLICABLE REQUIREMENTS FOR REFERENCE AND EQUIVALENT
METHODS FOR AIR MONITORING OF CRITERIA POLLUTANTS—Continued
Pollutant
Reference or equivalent
Equivalent Class I .................................
Equivalent Class II ................................
Equivalent Class III ...............................
1 Some
Manual or
automated
Applicable
appendix of
part 50 of
this chapter
Applicable subparts of this part
A
B
C
D
E
F
Manual ........
Manual ........
Automated ...
L, O 2 .....................
L, O 2 .....................
L,1 O 1 2 .................
✓
✓
✓
..........
..........
..........
✓
✓2
✓
..........
..........
..........
✓
✓
✓
..........
✓12
✓1
requirements may apply, based on the nature of each particular candidate method, as determined by the Administrator.
Class III requirements may be substituted.
2 Alternative
Subpart B—Procedures for Testing
Performance Characteristics of
Automated Methods for SO2, CO, O3,
and NO2
11. Amend table B–1 to subpart B of
part 53 by revising footnote 4 to read as
follows:
khammond on DSKJM1Z7X2PROD with PROPOSALS3
■
VerDate Sep<11>2014
20:11 Jan 26, 2023
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Table B–1 to Subpart B of Part 53—
Performance Limit Specifications for
Automated Methods
*
*
*
*
nitric oxide interference for the SO2
ultraviolet fluorescence (UVF) method,
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*
*
*
*
*
12. Revise table B–3 to subpart B of
part 53 to read as follows:
■
*
4 For
interference equivalent is ±0.003 ppm for the
lower range.
E:\FR\FM\27JAP3.SGM
27JAP3
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..........
..........
..........
..........
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Ultraviolet fluorescence .......
Flame photometric ...............
Gas chromatography ...........
Spectrophotometric-wet
chemical (pararosanaline).
Electrochemical ...................
Conductivity .........................
Spectrophotometric-gas
phase, including DOAS.
Ethylene
Chemiluminescence.
NO- chemiluminescence .....
Electrochemical ...................
Spectrophotometric-wet
chemical (potassium iodide).
Spectrophotometric-gas
phase, including ultraviolet
absorption and DOAS.
Non-dispersive Infrared .......
Gas chromatography with
flame ionization detector.
Electrochemical ...................
Catalytic combustion-thermal detection.
IR fluorescence ....................
Mercury replacement-UV
photometric.
Chemiluminescent ...............
Spectrophotometric-wet
chemical (azo-dye reaction).
Electrochemical ...................
Spectrophotometric-gas
phase.
Analyzer type 2
0.2
..................
..................
..................
..................
..................
..................
..................
..................
..................
..................
..................
..................
..................
..................
0.2
0.2
..................
..................
..................
..................
0.2
Hydrochloric
acid
3 0.1
................
................
................
................
3 0.1
..................
3 0.1
................
................
................
................
................
................
................
0.5
0.5
0.5
0.5
..............
..............
..............
..............
..............
..............
0.5
..............
0.5
0.5
3 0.1
................
................
..............
3 0.1
4 0.14
4 0.14
4 0.14
4 0.1
4 0.1
4 0.1
4 0.1
................
................
................
................
................
................
0.5
0.5
0.5
0.5
................
0.5
0.5
0.5
4 0.14
0.1
................
................
4 0.14
4 0.14
0.5
................
................
0.5
4 0.14
Nitrogen
dioxide
0.01
0.1
0.1
Sulfur
dioxide
5 0.1
Hydrogen
sulfide
..................
..................
..................
0.1
..................
..................
..................
..................
3 0.1
3 0.1
..................
0.1
0.1
..................
..................
..................
..................
0.1
Ammonia
0.5
0.5
0.5
0.5
............
............
0.5
............
750
..............
..............
750
750
..............
..............
750
750
..............
..............
3 0.5
............
............
750
..............
..............
750
..............
750
..............
..............
750
750
750
Carbon
dioxide
............
............
3 0.5
............
0.5
............
0.5
0.5
............
............
............
Nitric
oxide
................
................
................
................
................
0.2
0.2
0.2
................
................
................
................
................
................
................
0.2
................
................
................
................
................
................
Ethylene
0.5
0.5
..........
0.5
..........
..........
..........
..........
..........
..........
4 0.08
4 0.08
4 0.08
4 0.08
4 0.08
0.5
..........
0.5
0.5
..........
..........
0.5
Ozone
................
................
................
................
................
................
................
................
................
................
0.02
................
................
................
................
................
................
0.2
0.2
................
................
................
M-xylene
20,000
20,000
20,000
................
20,000
................
20,000
20,000
20,000
20,000
20,000
................
3 20,000
3 20,000
3 20,000
3 20,000
................
................
3 20,000
................
3 20,000
20,000
Water
vapor
50
50
..............
..............
4 10
............
............
............
............
............
............
4 10
4 10
............
5.0
............
............
............
............
............
............
............
............
............
............
............
............
............
............
Methane
4 10
4 10
4 10
..............
..............
..............
..............
..............
..............
..............
..............
..............
50
50
..............
Carbon
monoxide
TABLE B–3 TO SUBPART B OF PART 53—INTERFERENT TEST CONCENTRATION,1 PARTS PER MILLION
..............
..............
..............
..............
0.5
0.5
..............
0.5
..............
0.5
..............
..............
..............
..............
..............
..............
..............
..............
..............
..............
..............
..............
Ethane
..............
..............
..............
..............
..............
..............
..............
..............
..............
..............
..............
..............
..............
..............
..............
..............
..............
..............
6 0.05
..............
..............
..............
Naphthalene
2 Analyzer
1 Concentrations
of interferent listed must be prepared and controlled to ±10 percent of the stated value.
types not listed will be considered by the Administrator as special cases.
3 Do not mix interferent with the pollutant.
4 Concentration of pollutant used for test. These pollutant concentrations must be prepared to ±10 percent of the stated value.
5 If candidate method utilizes an elevated-temperature scrubber for removal of aromatic hydrocarbons, perform this interference test.
6 If naphthalene test concentration cannot be accurately quantified, remove the scrubber, use a test concentration that causes a full-scale response, reattach the scrubber, and evaluate response for interference.
NO2 ..........
NO2 ..........
NO2 ..........
NO2 ..........
CO ............
CO ............
CO ............
CO ............
CO ............
CO ............
O3 .............
O3 .............
O3 .............
O3 .............
O3 .............
SO2 ..........
SO2 ..........
SO2 ..........
SO2
SO2
SO2
SO2
Pollutant
khammond on DSKJM1Z7X2PROD with PROPOSALS3
5698
Federal Register / Vol. 88, No. 18 / Friday, January 27, 2023 / Proposed Rules
E:\FR\FM\27JAP3.SGM
27JAP3
5699
Federal Register / Vol. 88, No. 18 / Friday, January 27, 2023 / Proposed Rules
13. Amend appendix A to subpart B
of part 53 by revising figures B–3 and
B–5 to read as follows:
Appendix A to Subpart B of Part 53—
Optional Forms for Reporting Test
Results
■
*
*
*
*
Figure B–3 to Appendix A to Subpart B
of Part 53—Form for Test Data and
Calculations for Lower Detectable Limit
(LDL) and Interference Equivalent (IE)
(see § 53.23(c) and (d))
*
BILLING CODE 6560–50–P
LDL and INTERFERENCE TEST DATA
Applicant_ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ __
Analyzer_ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ __
TEST
PARAMETER
READING or
CAlCUlATlON
LOWER
DETECTABLE LIMIT
Date._ _ _ _ _ _ _ _ _ _ __
Pollutant'"-----------
TEST NUMBER
1
2
3
4
5
6
7
8
9
10
11
12
13
14
15
a.
a..
LDL=S..-Bz
R,
1
Ru
IE=R11-R,
R,
R,.
IE=R,.-R,
2
R•
R,.
IE=R,.-R,
R,
3•
INTERFERENCE
EQUIVAlENT
4•
Ru
.IE=R,.-R,
Rs
R,.
s•
IE=R..-R.
fl
TOTAL*
LIIB1I
i=l
*If required.
BILLING CODE 6560–50–C
*
*
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*
*
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27JAP3
EP27JA23.006
khammond on DSKJM1Z7X2PROD with PROPOSALS3
*
5700
Federal Register / Vol. 88, No. 18 / Friday, January 27, 2023 / Proposed Rules
Figure B–5 to Appendix A to Subpart B
of Part 53—Form for Calculating Zero
Drift, Span Drift and Precision (see
§ 53.23(e))
CALCULATION OF ZERO DRIFT, SPAN DRIFT, AND PRECISION
Applicant._ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ __
Date_ _ _ _ _ _ _ _ _ _ __
Analyzer_ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ __
Pollutant._ _ _ _ _ _ _ _ _ __
TESTDAY(n)
TEST
CALCULATION
PARAMETER
12
HOUR
ZERO
DRIFT
1
2
3
4
5
6
7
8
9
10
11
12
13
14
15
12ZD=C,.,,.-C,,,,,,
Z ={L, + L,J/2
24
HOUR
24ZD=z.-z._,
24ZD=Z'.-Z'~,
S,. -S,._1
SD,,.=---
SPAN
24
DRIFT
HOUR
Sn-1
X100%
SDn
= Sn -S'n-1
S',._1
x100%
20%
URL
PRECISION
(P:w)
80%
URL
(Pao)
*
*
*
*
P20 =%STANDARD
DEVIATION of (P,•.•P.)
P20=%STANDARD
DEVIATION of {P,.••Pu)
§ 53.35 Test procedure for Class II and
Class III methods for PM2.5 and PM10–2.5.
*
Subpart C—Procedures for
Determining Comparability Between
Candidate Methods and Reference
Methods
*
14. Amend § 53.35 by revising
paragraph (b)(1)(ii)(D) to read as follows:
■
*
*
(b) * * *
(1) * * *
(ii) * * *
*
*
(D) Site D shall be in a large city east
of the Mississippi River, having
characteristically high humidity levels.
*
*
*
*
*
■ 15. Revise table C–4 to subpart C of
part 53 to read as follows:
TABLE C–4 TO SUBPART C OF PART 53—TEST SPECIFICATIONS FOR PM10, PM2.5, AND PM10–2.5 CANDIDATE
EQUIVALENT METHODS
PM2.5
Acceptable concentration
range (Rj), μg/m3.
Minimum number of test
sites.
Minimum number of candidate method samplers
or analyzers per site.
Number of reference
method samplers per
site.
Minimum number of acceptable sample sets
per site for PM10 methods:
Rj <20 μg/m3 ............
Rj >20 μg/m3 ............
Total ...................
VerDate Sep<11>2014
PM10–2.5
PM10
Class I
Class II
Class III
Class II
Class III
5–300 .........
3–200 .........
3–200 .............................
3–200 .............................
3–200 .............................
3–200.
2 .................
1 .................
2 .....................................
4 .....................................
2 .....................................
4.
3 .................
3 .................
13
..................................
13
..................................
13
..................................
1 3.
3 .................
3 .................
13
..................................
13
..................................
13
..................................
1 3.
3.
3.
10.
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27JAP3
EP27JA23.007
khammond on DSKJM1Z7X2PROD with PROPOSALS3
Specification
5701
Federal Register / Vol. 88, No. 18 / Friday, January 27, 2023 / Proposed Rules
TABLE C–4 TO SUBPART C OF PART 53—TEST SPECIFICATIONS FOR PM10, PM2.5, AND PM10–2.5 CANDIDATE
EQUIVALENT METHODS—Continued
PM2.5
Specification
Minimum number of acceptable sample sets
per site for PM2.5 and
PM10–2.5 candidate
equivalent methods:
Rj <15 μg/m3 for 24hr or Rj <8 μg/m3
for 48-hr samples.
Rj>15 μg/m3 for 24-hr
or Rj >8 μg/m3 for
48-hr samples.
Each season .............
Total, each site ..
Precision of replicate reference method measurements, PRj or RPRj,
respectively; RP for
Class II or III PM2.5 or
PM10–2.5, maximum.
Precision of PM2.5 or
PM10–2.5 candidate
method, CP, each site.
Slope of regression relationship.
Intercept of regression relationship, μg/m3.
Correlation of reference
method and candidate
method measurements.
1 Some
PM10–2.5
PM10
Class I
Class II
Class III
Class II
Class III
....................
3 .................
3 .....................................
3 .....................................
3 .....................................
3.
....................
3 .................
3 .....................................
3 .....................................
3 .....................................
3.
....................
10 ...............
23 ...................................
23 ...................................
23 ...................................
23.
....................
10 ...............
23 ...................................
23 ...................................
5 μg/m3 or
7%.
2 μg/m3 or
5%.
10% 2 .............................
23 (46 for two-season
sites).
10% 2 .............................
10% 2 .............................
23 (46 for two-season
sites).
10%.2
....................
....................
10% 2 .............................
15% 2 .............................
15% 2 .............................
15%.2
1 ±0.10 .......
1 ±0.05 .......
1 ±0.10 ..........................
1 ±0.10 ..........................
1 ±0.10 ..........................
1 ±0.12.
0 ±5 ............
0 ±1 ............
Between: 13.55¥(15.05
× slope), but not less
than¥1.5; and
16.56¥(15.05 ×
slope), but not more
than +1.5.
Between: 15.05¥(17.32
× slope), but not less
than¥2.0; and
15.05¥(13.20 ×
slope), but not more
than +2.0.
Between: 62.05¥(70.5 ×
slope), but not less
than¥3.5; and
78.95¥(70.5 × slope),
but not more than
+3.5.
Between: 70.50¥(82.93
× slope), but not less
than¥7.0; and
70.50¥(61.16 ×
slope), but not more
than +7.0.
≥0.97 ..........
≥0.97 ..........
≥0.93—for CCV ≤0.4; ≥0.85 + 0.2 × CCV—for 0.4 ≤ CCV ≤0.5; ≥0.95—for CCV ≥0.5.
missing daily measurement values may be permitted; see test procedure.
as the root mean square over all measurement sets.
2 Calculated
§ 53.43
Subpart D—Procedures for Testing
Performance Characteristics of
Methods for PM10
(a) * * *
(2) * * *
khammond on DSKJM1Z7X2PROD with PROPOSALS3
*
*
*
VerDate Sep<11>2014
*
*
20:11 Jan 26, 2023
(xvi) * * *
(c) * * *
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(iv) * * *
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27JAP3
EP27JA23.008
16. Amend § 53.43 by revising the
formula in paragraph (a)(2)(xvi) and
paragraph (c)(2)(iv) to read as follows:
■
Test procedures.
5702
Federal Register / Vol. 88, No. 18 / Friday, January 27, 2023 / Proposed Rules
if Cj is below 80 µg/m 3 , or
or will be routinely implemented, and
that an appropriate procedure is in
place for the disposition of units that
fail this tolerance tests.
*
*
*
*
*
Subpart F—Procedures for Testing
Performance Characteristics of Class II
Equivalent Methods for PM2.5
17. Amend § 53.51 by revising
paragraph (d)(2) to read as follows:
■
*
*
*
*
*
(d) * * *
(2) VSCC and TE–PM2.5C separators.
For samplers and monitors utilizing the
BGI VSCC or Tisch TE–PM2.5C particle
size separators specified in sections
7.3.4.4 and 7.3.4.5 of appendix L to part
50 of this chapter, respectively, the
respective manufacturers shall identify
the critical dimensions and
manufacturing tolerances for the
separator, devise appropriate test
procedures to verify that the critical
dimensions and tolerances are
maintained during the manufacturing
process, and carry out those procedures
on each separator manufactured to
verify conformance of the manufactured
products. The manufacturer shall also
maintain records of these tests and their
test results and submit evidence that
this procedure is incorporated into the
manufacturing procedure, that the test is
khammond on DSKJM1Z7X2PROD with PROPOSALS3
Cvol
Where:
Vu = uranine volume, ml;
Voleic = oleic acid volume, ml;
Vsol = total solution volume, ml;
Mu = uranine mass, g;
Pu = uranine density, g/cm3;
Moleic = oleic acid mass, g; and
Poleic = oleic acid density, g/cm3.
*
*
*
*
*
18. Amend § 53.61 by revising the
heading of paragraph (g) and paragraphs
(g)(1) introductory text, (g)(1)(i)
introductory text, and (g)(2)(i) and
adding paragraph (g)(2)(iii) to read as
follows:
■
§ 53.51 Demonstration of compliance with
design specifications and manufacturing
and test requirements.
§ 53.61
*
*
*
*
(g) Vibrating Orifice Aerosol
Generator (VOAG) and Flow-Focusing
Monodisperse Aerosol Generator
(FMAG) conventions. * * *
(1) Particle aerodynamic diameter.
The VOAG and FMAG produce nearmonodisperse droplets through the
controlled breakup of a liquid jet. When
the liquid solution consists of a nonvolatile solute dissolved in a volatile
solvent, the droplets dry to form
particles of near-monodisperse size.
(i) The physical diameter of a
generated spherical particle can be
calculated from the operational
parameters of the VOAG and FMAG as:
*
*
*
*
*
=
Vu+ Voleic
20:11 Jan 26, 2023
Jkt 259001
V.
sol
Equation 5 to Paragraph (g)(2)(iii)
(Mu/ Pu)+ (Moleic/ Poleic)
Vsol
Authority: 42 U.S.C. 7403, 7405, 7410,
7414, 7601, 7611, 7614, and 7619.
a. By removing the definition for
‘‘Approved regional method (ARM)’’;
and
■ b. By revising the definition for
‘‘Traceable.’’
The revision reads as follows:
Subpart A—General Provisions
§ 58.1
PART 58—AMBIENT AIR QUALITY
SURVEILLANCE
19. The authority citation for part 58
continues to read as follows:
■
■
VerDate Sep<11>2014
Test conditions.
*
20. Amend § 58.1 as follows:
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*
E:\FR\FM\27JAP3.SGM
Definitions.
*
*
27JAP3
*
*
EP27JA23.010
Subpart E—Procedures for Testing
Physical (Design) and Performance
Characteristics of Reference Methods
and Class I and Class II Equivalent
Methods for PM2.5 or PM10–2.5
(2) * * *
(i) Solid particle tests performed in
this subpart shall be conducted using
particles composed of ammonium
fluorescein. For use in the VOAG or
FMAG, liquid solutions of known
volumetric concentration can be
prepared by diluting fluorescein powder
(C2OH12O5, FW = 332.31, CAS 2321–07–
5) with aqueous ammonia. Guidelines
for preparation of fluorescein solutions
of the desired volume concentration
(Cvol) are presented in Vanderpool and
Rubow (1988) (Reference 2 in appendix
A to this subpart). For purposes of
converting particle physical diameter to
aerodynamic diameter, an ammonium
fluorescein particle density of 1.35 g/
cm3 shall be used.
*
*
*
*
*
(iii) Calculation of the physical
diameter of the particles produced by
the VOAG and FMAG requires
knowledge of the liquid solution’s
volume concentration (Cvol). Because
uranine is essentially insoluble in oleic
acid, the total particle volume is the
sum of the oleic acid volume and the
uranine volume. The volume
concentration of the liquid solution
shall be calculated as:
EP27JA23.009
if C¯j is above 80 mg/m3.
Federal Register / Vol. 88, No. 18 / Friday, January 27, 2023 / Proposed Rules
Traceable means a measurement
result from a local standard whereby the
result can be related to the International
System of Units (SI) through a
documented unbroken chain of
calibrations, each contributing to the
measurement uncertainty. Traceable
measurement results must be compared
and certified, either directly or via not
more than one intermediate standard, to
a National Institute of Standards and
Technology (NIST)-certified reference
standard. Examples include but are not
limited to NIST Standard Reference
Material (SRM), NIST-traceable
Reference Material (NTRM), or a NISTcertified Research Gas Mixture (RGM).
Traceability to the SI through other
National Metrology Institutes (NMIs) in
addition to NIST is allowed if a
Declaration of Equivalence (DoE) exists
between NIST and that NMI.
*
*
*
*
*
Subpart B—Monitoring Network
21. Amend § 58.10 as follows:
a. By revising paragraphs (a)(1) and
(b)(10) and (13);
■ b. By adding paragraph (b)(14); and
■ c. By revising paragraph (d).
The revisions and addition read as
follows:
■
■
khammond on DSKJM1Z7X2PROD with PROPOSALS3
§ 58.10 Annual monitoring network plan
and periodic network assessment.
(a)(1) Beginning July 1, 2007, the
state, or where applicable local, agency
shall submit to the Regional
Administrator an annual monitoring
network plan which shall provide for
the documentation of the establishment
and maintenance of an air quality
surveillance system that consists of a
network of SLAMS monitoring stations
that can include FRM and FEM
monitors that are part of SLAMS, NCore,
CSN, PAMS, and SPM stations. The
plan shall include a statement of
whether the operation of each monitor
meets the requirements of appendices
A, B, C, D, and E to this part, where
applicable. The Regional Administrator
may require additional information in
support of this statement. The annual
monitoring network plan must be made
available for public inspection and
comment for at least 30 days prior to
submission to the EPA and the
submitted plan shall include and
address, as appropriate, any received
comments.
*
*
*
*
*
(b) * * *
(10) Any monitors for which a waiver
has been requested or granted by the
EPA Regional Administrator as allowed
for under appendix D or appendix E to
this part. For those monitors where a
VerDate Sep<11>2014
20:11 Jan 26, 2023
Jkt 259001
waiver has been approved, the annual
monitoring network plan shall include
the date the waiver was approved.
*
*
*
*
*
(13) The identification of any PM2.5
FEMs used in the monitoring agency’s
network where the data are not of
sufficient quality such that data are not
to be compared to the national ambient
air quality standards (NAAQS). For
required SLAMS where the agency
identifies that the PM2.5 Class III FEM
does not produce data of sufficient
quality for comparison to the NAAQS,
the monitoring agency must ensure that
an operating FRM or filter-based FEM
meeting the sample frequency
requirements described in § 58.12 or
other Class III PM2.5 FEM with data of
sufficient quality is operating and
reporting data to meet the network
design criteria described in appendix D
to this part.
(14) The identification of any site(s)
intended to address being sited in an atrisk community where there are
anticipated effects from sources in the
area as required in section 4.7.1(b)(3) of
appendix D to this part. An initial
approach to the question of whether any
new or moved sites are needed and to
identify the communities in which they
intend to add monitoring for meeting
the requirement in this paragraph
(b)(14), if applicable, shall be submitted
in accordance with the requirements of
section 4.7.1(b)(3) of appendix D to this
part which includes submission to the
EPA Regional Administrator no later
than July 1, 2024. Specifics on the
resulting proposed new or moved sites
for PM2.5 network design to address atrisk communities, if applicable, would
need to be detailed in annual
monitoring network plans due to each
applicable EPA Regional office no later
than July 1, 2025. The plan shall
provide for any required sites to be
operational no later than 24 months
from date of approval of a plan or
January 1, 2027, whichever comes first.
*
*
*
*
*
(d) The state, or where applicable
local, agency shall perform and submit
to the EPA Regional Administrator an
assessment of the air quality
surveillance system every 5 years to
determine, at a minimum, if the network
meets the monitoring objectives defined
in appendix D to this part, whether new
sites are needed, whether existing sites
are no longer needed and can be
terminated, and whether new
technologies are appropriate for
incorporation into the ambient air
monitoring network. The network
assessment must consider the ability of
existing and proposed sites to support
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5703
air quality characterization for areas
with relatively high populations of
susceptible individuals (e.g., children
with asthma) and other at-risk
populations, and, for any sites that are
being proposed for discontinuance, the
effect on data users other than the
agency itself, such as nearby states and
tribes or health effects studies. The
state, or where applicable local, agency
must submit a copy of this 5-year
assessment, along with a revised annual
network plan, to the Regional
Administrator. The assessments are due
every five years beginning July 1, 2010.
*
*
*
*
*
■ 22. Amend § 58.11 by revising
paragraphs (a)(2) and (e) to read as
follows:
§ 58.11
Network technical requirements.
(a) * * *
(2) Beginning January 1, 2009, state
and local governments shall follow the
quality assurance criteria contained in
appendix A to this part that apply to
SPM sites when operating any SPM site
which uses an FRM or an FEM and
meets the requirements of appendix E to
this part, unless the Regional
Administrator approves an alternative to
the requirements of appendix A with
respect to such SPM sites because
meeting those requirements would be
physically and/or financially
impractical due to physical conditions
at the monitoring site and the
requirements are not essential to
achieving the intended data objectives
of the SPM site. Alternatives to the
requirements of appendix A may be
approved for an SPM site as part of the
approval of the annual monitoring plan,
or separately.
*
*
*
*
*
(e) State and local governments must
assess data from Class III PM2.5 FEM
monitors operated within their network
using the performance criteria described
in table C–4 to subpart C of part 53 of
this chapter, for cases where the data are
identified as not of sufficient
comparability to a collocated FRM, and
the monitoring agency requests that the
FEM data should not be used in
comparison to the NAAQS. These
assessments are required in the
monitoring agency’s annual monitoring
network plan described in § 58.10(b) for
cases where the FEM is identified as not
of sufficient comparability to a
collocated FRM. For these collocated
PM2.5 monitors, the performance criteria
apply with the following additional
provisions:
(1) The acceptable concentration
range (Rj), mg/m3 may include values
down to 0 mg/m3.
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(2) The minimum number of test sites
shall be at least one; however, the
number of test sites will generally
include all locations within an agency’s
network with collocated FRMs and
FEMs.
(3) The minimum number of methods
shall include at least one FRM and at
least one FEM.
(4) Since multiple FRMs and FEMs
may not be present at each site, the
precision statistic requirement does not
apply, even if precision data are
available.
(5) All seasons must be covered with
no more than 36 consecutive months of
data in total aggregated together.
(6) The key statistical metric to
include in an assessment is the bias
(both additive and multiplicative) of the
PM2.5 continuous FEM(s) compared to a
collocated FRM(s). Correlation is
required to be reported in the
assessment, but failure to meet the
correlation criteria, by itself, is not
cause to exclude data from a continuous
FEM monitor.
■ 23. Amend § 58.12 by revising
paragraphs (d)(1) and (3) to read as
follows:
§ 58.12
Operating schedules.
khammond on DSKJM1Z7X2PROD with PROPOSALS3
*
*
*
*
*
(d) * * *
(1)(i) Manual PM2.5 samplers at
required SLAMS stations without a
collocated continuously operating PM2.5
monitor must operate on at least a 1-in3 day schedule unless a waiver for an
alternative schedule has been approved
per paragraph (d)(1)(ii) of this section.
(ii) For SLAMS PM2.5 sites with both
manual and continuous PM2.5 monitors
operating, the monitoring agency may
request approval for a reduction to 1-in6 day PM2.5 sampling or for seasonal
sampling from the EPA Regional
Administrator. Other requests for a
reduction to 1-in-6 day PM2.5 sampling
or for seasonal sampling may be
approved on a case-by-case basis. The
EPA Regional Administrator may grant
sampling frequency reductions after
consideration of factors (including but
not limited to the historical PM2.5 data
quality assessments, the location of
current PM2.5 design value sites, and
their regulatory data needs) if the
Regional Administrator determines that
the reduction in sampling frequency
will not compromise data needed for
implementation of the NAAQS.
Required SLAMS stations whose
measurements determine the design
value for their area and that are within
plus or minus 10 percent of the annual
NAAQS, and all required sites where
one or more 24-hour values have
exceeded the 24-hour NAAQS each year
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20:11 Jan 26, 2023
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for a consecutive period of at least 3
years are required to maintain at least a
1-in-3 day sampling frequency until the
design value no longer meets the criteria
in this paragraph (d)(1)(ii) for 3
consecutive years. A continuously
operating FEM PM2.5 monitor satisfies
the requirement in this paragraph
(d)(1)(ii) unless it is identified in the
monitoring agency’s annual monitoring
network plan as not appropriate for
comparison to the NAAQS and the EPA
Regional Administrator has approved
that the data from that monitor may be
excluded from comparison to the
NAAQS.
(iii) Required SLAMS stations whose
measurements determine the 24-hour
design value for their area and whose
data are within plus or minus 5 percent
of the level of the 24-hour PM2.5 NAAQS
must have an FRM or FEM operate on
a daily schedule if that area’s design
value for the annual NAAQS is less than
the level of the annual PM2.5 standard.
A continuously operating FEM or PM2.5
monitor satisfies the requirement in this
paragraph (d)(1)(iii) unless it is
identified in the monitoring agency’s
annual monitoring network plan as not
appropriate for comparison to the
NAAQS and the EPA Regional
Administrator has approved that the
data from that monitor may be excluded
from comparison to the NAAQS. The
daily schedule must be maintained until
the referenced design values no longer
meets the criteria in this paragraph
(d)(1)(iii) for 3 consecutive years.
(iv) Changes in sampling frequency
attributable to changes in design values
shall be implemented no later than
January 1 of the calendar year following
the certification of such data as
described in § 58.15.
*
*
*
*
*
■ 24. Revise § 58.15 to read as follows:
§ 58.15 Annual air monitoring data
certification.
(a) The state, or where appropriate
local, agency shall submit to the EPA
Regional Administrator an annual air
monitoring data certification letter to
certify data collected by FRM and FEM
monitors at SLAMS and SPM sites that
meet criteria in appendix A to this part
from January 1 to December 31 of the
previous year. The head official in each
monitoring agency, or his or her
designee, shall certify that the previous
year of ambient concentration and
quality assurance data are completely
submitted to AQS and that the ambient
concentration data are accurate to the
best of her or his knowledge, taking into
consideration the quality assurance
findings. The annual data certification
letter is due by May 1 of each year.
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(b) Along with each certification
letter, the state shall submit to the
Regional Administrator an annual
summary report of all the ambient air
quality data collected by FRM and FEM
monitors at SLAMS and SPM sites. The
annual report(s) shall be submitted for
data collected from January 1 to
December 31 of the previous year. The
annual summary serves as the record of
the specific data that is the object of the
certification letter.
(c) Along with each certification
letter, the state shall submit to the
Regional Administrator a summary of
the precision and accuracy data for all
ambient air quality data collected by
FRM and FEM monitors at SLAMS and
SPM sites. The summary of precision
and accuracy shall be submitted for data
collected from January 1 to December 31
of the previous year.
Subpart C—Special Purpose Monitors
25. Amend § 58.20 by revising
paragraphs (b) through (e) to read as
follows:
■
§ 58.20
Special purpose monitors (SPM).
*
*
*
*
*
(b) Any SPM data collected by an air
monitoring agency using a Federal
reference method (FRM) or Federal
equivalent method (FEM) must meet the
requirements of §§ 58.11 and 58.12 and
appendix A to this part or an approved
alternative to appendix A. Compliance
with appendix E to this part is optional
but encouraged except when the
monitoring agency’s data objectives are
inconsistent with the requirements in
appendix E. Data collected at an SPM
using a FRM or FEM meeting the
requirements of appendix A must be
submitted to AQS according to the
requirements of § 58.16. Data collected
by other SPMs may be submitted. The
monitoring agency must also submit to
AQS an indication of whether each SPM
reporting data to AQS monitor meets the
requirements of appendices A and E.
(c) All data from an SPM using an
FRM or FEM which has operated for
more than 24 months are eligible for
comparison to the relevant NAAQS,
subject to the conditions of §§ 58.11(e)
and 58.30, unless the air monitoring
agency demonstrates that the data came
from a particular period during which
the requirements of appendix A,
appendix C, or appendix E to this part
were not met, subject to review and EPA
Regional Office approval as part of the
annual monitoring network plan
described in § 58.10.
(d) If an SPM using an FRM or FEM
is discontinued within 24 months of
start-up, the Administrator will not base
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2.6.1.1 The concentrations of EPA
Protocol Gas standards used for ambient air
monitoring must be certified with a 95percent confidence interval to have an
analytical uncertainty of no more than ±2.0
percent (inclusive) of the certified
concentration (tag value) of the gas mixture.
The uncertainty must be calculated in
accordance with the statistical procedures
defined in Reference 4 of this appendix.
2.6.1.2 Specialty gas producers
advertising certification with the procedures
provided in Reference 4 of this appendix and
distributing gases as ‘‘EPA Protocol Gas’’ for
ambient air monitoring purposes must adhere
to the regulatory requirements specified in 40
CFR 75.21(g) or not use ‘‘EPA’’ in any form
of advertising. Monitoring organizations must
provide information to the EPA on the
specialty gas producers they use on an
annual basis. PQAOs, when requested by the
EPA, must participate in the EPA Ambient
Air Protocol Gas Verification Program at least
once every 5 years by sending a new unused
standard to a designated verification
laboratory.
*
*
*
*
*
*
*
*
*
*
*
k
k
X Li=l ti2 -
('°k
)2
Lli=l ti
*
*
*
4.2.5 Performance Evaluation Programs
Bias Estimate for PM2.5. The bias estimate is
calculated using the PEP audits described in
'°n
100 "'
khammond on DSKJM1Z7X2PROD with PROPOSALS3
*
where
Li=l si
n,,/NAAQS concentration
*
*
*
*
*
6. References
(1) American National Standard Institute—
Quality Management Systems For
Environmental Information And Technology
Programs—Requirements With Guidance For
VerDate Sep<11>2014
20:11 Jan 26, 2023
Jkt 259001
si
*
*
*
Where Xi is the concentration from the
primary sampler and Yi is the concentration
value from the audit sampler. The coefficient
of variation upper bound is calculated using
equation 7 to this appendix:
Equation 7 to Appendix A to Part 58
section 3.2.4. of this appendix. The bias
estimator is based on, si, the absolute
difference in concentrations divided by the
square root of the PEP concentration.
Equation 8 to Appendix A to Part 58
meas - audit
= - - - - - x 100
·
,!audit
Use. ASQ/ANSI E4–2014. February 2014.
Available from ANSI Webstore https://
webstore.ansi.org/.
*
*
Standards. EPA–600/R–12/531. May, 2012.
Available from U.S. Environmental
Protection Agency, National Risk
Management Research Laboratory, Research
(4) EPA Traceability Protocol for Assay and
Certification of Gaseous Calibration
PO 00000
Frm 00149
Fmt 4701
*
NAAQS Concentration* Xli,k-1
denominator adjusts for the fact that each ti
is calculated from two values with error.
*
*
k-1
X
Zk(k-1)
Where k is the number of valid data pairs
being aggregated, and X20.1,k-1 is the 10th
percentile of a chi-squared distribution with
k-1 degrees of freedom. The factor of 2 in the
*
*
3.2.4 PM2.5 Performance Evaluation
Program (PEP) Procedures. The PEP is an
independent assessment used to estimate
total measurement system bias. These
evaluations will be performed under the
national performance evaluation program
(NPEP) as described in section 2.4 of this
appendix or a comparable program. A
prescribed number of Performance evaluation
2.6.1 Gaseous pollutant concentration
standards (permeation devices or cylinders of
compressed gas) used to obtain test
concentrations for CO, SO2, NO, and NO2
must be EPA Protocol Gases certified in
accordance with one of the procedures given
in Reference 4 of this appendix.
*
4.2.1 Collocated Quality Control Sampler
Precision Estimate for PM10, PM2.5, and Pb.
Precision is estimated via duplicate
measurements from collocated samplers. It is
recommended that the precision be
aggregated at the PQAO level quarterly,
annually, and at the 3-year level. The data
pair would only be considered valid if both
concentrations are greater than or equal to
the minimum values specified in section 4(c)
of this appendix. For each collocated data
pair, calculate ti, using equation 6 to this
appendix:
Equation 6 to Appendix A to Part 58
Sfmt 4702
E:\FR\FM\27JAP3.SGM
27JAP3
EP27JA23.013
Appendix A to Part 58—Quality
Assurance Requirements for Monitors
Used in Evaluations of National
Ambient Air Quality Standards
*
*
3.1.3.3 Using audit gases that are verified
against the NIST standard reference methods
or special review procedures and validated
per the certification periods specified in
Reference 4 of this appendix (EPA
Traceability Protocol for Assay and
Certification of Gaseous Calibration
Standards) for CO, SO2, and NO2 and using
O3 analyzers that are verified quarterly
against a standard reference photometer.
*
EP27JA23.012
*
sampling events will be performed annually
within each PQAO. For PQAOs with less
than or equal to five monitoring sites, five
valid performance evaluation audits must be
collected and reported each year. For PQAOs
with greater than five monitoring sites, eight
valid performance evaluation audits must be
collected and reported each year. A valid
performance evaluation audit means that
both the primary monitor and PEP audit
concentrations are valid and equal to or
greater than 2 mg/m3. Siting of the PEP
monitor must be consistent with section
3.2.3.4(c) of this appendix. However, any
horizontal distance greater than 4 meters and
any vertical distance greater than one meter
must be reported to the EPA regional PEP
coordinator. Additionally for every monitor
designated as a primary monitor, a primary
quality assurance organization must:
EP27JA23.011
a NAAQS violation determination for
the PM2.5 or ozone NAAQS solely on
data from the SPM.
(e) If an SPM using an FRM or FEM
is discontinued within 24 months of
start-up, the Administrator will not
designate an area as nonattainment for
the CO, SO2, NO2, or 24-hour PM10
NAAQS solely on the basis of data from
the SPM. Such data are eligible for use
in determinations of whether a
nonattainment area has attained one of
these NAAQS.
*
*
*
*
*
■ 26. Amend appendix A to part 58 as
follows:
■ a. By revising section 2.6.1 and adding
sections 2.6.1.1 and 2.6.1.2;
■ b. By removing section 3.1.2.2 and
redesignating sections 3.1.2.3, 3.1.2.4,
3.1.2.5, and 3.1.2.6 as sections 3.1.2.2,
3.1.2.3, 3.1.2.4, and 3.1.2.5, respectively;
■ c. By revising sections 3.1.3.3, 3.2.4,
4.2.1, and 4.2.5; and
■ d. In section 6 by revising References
(1), (4), (6), (7), (9), (10), and (11) and
table A–1.
The revisions and additions read as
follows:
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Triangle Park, NC 27711. https://
www.epa.gov/nscep.
*
*
*
*
*
(6) List of Designated Reference and
Equivalent Methods. Available from U.S.
Environmental Protection Agency, Center for
Environmental Measurements and Modeling,
Air Methods and Characterization Division,
MD–D205–03, Research Triangle Park, NC
27711. https://www.epa.gov/amtic/airmonitoring-methods-criteria-pollutants.
(7) Transfer Standards for the Calibration
of Ambient Air Monitoring Analyzers for
Ozone. EPA–454/B–13–004 U.S.
Environmental Protection Agency, Research
Triangle Park, NC 27711, October, 2013.
https://www.epa.gov/sites/default/files/202009/documents/
ozonetransferstandardguidance.pdf.
*
*
*
*
*
(9) Quality Assurance Handbook for Air
Pollution Measurement Systems, Volume 1—
A Field Guide to Environmental Quality
Assurance. EPA–600/R–94/038a. April 1994.
Available from U.S. Environmental
Protection Agency, ORD Publications Office,
Center for Environmental Research
Information (CERI), 26 W. Martin Luther
King Drive, Cincinnati, OH 45268. https://
www.epa.gov/amtic/ambient-air-monitoringquality-assurance#documents.
(10) Quality Assurance Handbook for Air
Pollution Measurement Systems, Volume II:
Ambient Air Quality Monitoring Program
Quality System Development. EPA–454/B–
13–003. https://www.epa.gov/amtic/ambientair-monitoring-qualityassurance#documents.
(11) National Performance Evaluation
Program Standard Operating Procedures.
https://www.epa.gov/amtic/ambient-airmonitoring-quality-assurance#npep.
TABLE A–1 TO APPENDIX A TO PART 58—MINIMUM DATA ASSESSMENT REQUIREMENTS FOR NAAQS RELATED CRITERIA
POLLUTANT MONITORS
Method
Assessment method
Gaseous Methods (CO,
NO2, SO2, O3):
One-Point QC for
SO2, NO2, O3, CO.
Annual performance
evaluation for SO2,
NO2, O3, CO.
NPAP for SO2, NO2,
O3, CO.
Particulate Methods:
Continuous 4 method—collocated
quality control sampling PM2.5.
Manual method—collocated quality control sampling PM10,
PM2.5, Pb-TSP,
Pb-PM10.
Flow rate verification
PM10 (low Vol)
PM2.5, Pb-PM10.
Flow rate verification
PM10 (High-Vol),
Pb-TSP.
Semi-annual flow rate
audit PM10, TSP,
PM10-2.5, PM2.5,
Pb-TSP, Pb-PM10.
Pb analysis audits
Pb-TSP, Pb-PM10.
Minimum frequency
Parameters reported
Each analyzer .................
Response check at concentration 0.005–0.08
ppm SO2, NO2, O3,
and 0.5 and 5 ppm CO.
See section 3.1.2 of this
Each analyzer .................
appendix.
Once per 2 weeks 5 ........
Audit concentration 1 and
measured concentration 2.
One-Point QC.
Once per year ................
Annual PE.
Independent Audit ..........
20% of sites each year ..
Once per year ................
Audit concentration 1 and
measured concentration 2 for each level.
Audit concentration 1 and
measured concentration 2 for each level.
Collocated samplers .......
15% ................................
1-in-12 days ....................
No Transaction reported
as raw data.
Collocated samplers .......
15% ................................
1-in-12 days ....................
Primary sampler concentration and duplicate sampler concentration 3.
Primary sampler concentration and duplicate sampler concentration 3.
Check of sampler flow
rate.
Each sampler .................
Once every month 5 ........
Flow Rate Verification.
Check of sampler flow
rate.
Each sampler .................
Once every quarter 5 ......
Check of sampler flow
rate using independent
standard.
Each sampler .................
Once every 6 months 5 ...
Audit flow rate and
measured flow rate indicated by the sampler.
Audit flow rate and
measured flow rate indicated by the sampler.
Audit flow rate and
measured flow rate indicated by the sampler.
Check of analytical system with Pb audit
strips/filters.
Analytical ........................
Once each quarter 5 .......
Pb Analysis Audits.
(1) 5 valid audits for primary QA orgs, with ≤5
sites.
(2) 8 valid audits for primary QA orgs, with >5
sites.
(3) All samplers in 6
years.
(1) 1 valid audit and 4
collocated samples for
primary QA orgs, with
≤5 sites.
(2) 2 valid audits and 6
collocated samples for
primary QA orgs with
>5 sites.
Distributed over all 4
quarters 5.
Measured value and
audit value (ug Pb/filter) using AQS unit
code 077.
Primary sampler concentration and performance evaluation sampler concentration.
Performance Evalua- Collocated samplers .......
tion Program PM2.5.
khammond on DSKJM1Z7X2PROD with PROPOSALS3
Performance Evaluation Program PbTSP, Pb-PM10.
Collocated samplers .......
Coverage
Distributed over all 4
quarters 5.
Primary sampler concentration and performance evaluation sampler concentration. Primary sampler concentration and duplicate sampler concentration.
AQS assessment type
NPAP.
No Transaction reported
as raw data.
Flow Rate Verification.
Semi Annual Flow Rate
Audit.
PEP.
PEP.
1 Effective
concentration for open path analyzers.
concentration, if applicable for open path analyzers.
primary and collocated sampler values are reported as raw data.
4 PM
is
the
only particulate criteria pollutant requiring collocation of continuous and manual primary monitors.
2.5
5 EPA’s recommended maximum number of days that should exist between checks to ensure that the checks are routinely conducted over time and to limit data impacts resulting from a failed check.
2 Corrected
3 Both
*
*
*
VerDate Sep<11>2014
*
*
20:11 Jan 26, 2023
27. Amend appendix B to part 58 as
follows:
■
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a. By revising section 2.6.1 and adding
sections 2.6.1.1 and 2.6.1.2;
■
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of advertising. The PSD PQAOs must provide
information to the PSD reviewing authority
on the specialty gas producers they use (or
will use) for the duration of the PSD
monitoring project. This information can be
provided in the QAPP or monitoring plan,
but must be updated if there is a change in
the specialty gas producers used.
*
*
*
*
*
= 100 *
Where k is the number of valid data pairs
being aggregated, and X20.1,k¥1 is the 10th
percentile of a chi-squared distribution with
k¥1 degrees of freedom. The factor of 2 in
khammond on DSKJM1Z7X2PROD with PROPOSALS3
100
*
*
*
*
k
X
*
*
*
*
k ti2 - ("'k
)2
Li=l
Lii=l ti
X
*
*
*
ny NAAQS com::e11tmti1m
Jkt 259001
*
*
*
*
*
Frm 00151
Fmt 4701
*
Equation 6 to Appendix B to Part 58
Where Xi is the concentration from the
primary sampler and Yi is the concentration
value from the audit sampler. The coefficient
of variation upper bound is calculated using
equation 7 to this appendix:
Equation 7 to Appendix B to Part 58
section 3.2.4. of this appendix. The bias
estimator is based on, si, the absolute
difference in concentrations divided by the
square root of the PEP concentration.
Equation 8 to Appendix B to Part 58
Research Triangle Park, NC 27711.
https://www.epa.gov/nscep.
*
Sfmt 4702
*
meas-audit
,---==,.......
X 100
*
(4) EPA Traceability Protocol for Assay and
Certification of Gaseous Calibration
Standards. EPA–600/R–12/531. May,
2012. Available from U.S. Environmental
Protection Agency, National Risk
Management Research Laboratory,
PO 00000
*
. x2o.1,k-1
NAAQS Concentration*
4.2.5 Performance Evaluation Programs
Bias Estimate for PM2.5. The bias estimate is
calculated using the PEP audits described in
where s1
*
4.2.1 Collocated Quality Control Sampler
Precision Estimate for PM10, PM2.5, and Pb.
Precision is estimated via duplicate
measurements from collocated samplers. It is
recommended that the precision be
aggregated at the PQAO level quarterly,
annually, and at the 3-year level. The data
pair would only be considered valid if both
concentrations are greater than or equal to
the minimum values specified in section 4(c)
of this appendix. For each collocated data
pair, calculate ti, using equation 6 to this
appendix:
k-1
the denominator adjusts for the fact that each
ti is calculated from two values with error.
*
*
ANSI Webstore https://
webstore.ansi.org/.
(1) American National Standard Institute—
Quality Management Systems For
Environmental Information And
Technology Programs—Requirements
With Guidance For Use. ASQ/ANSI E4–
2014. February 2014. Available from
20:11 Jan 26, 2023
*
2k(k -1)
*
6. References
VerDate Sep<11>2014
*
3.2.4 PM2.5 Performance Evaluation
Program (PEP) Procedures. The PEP is an
independent assessment used to estimate
total measurement system bias. These
evaluations will be performed under the
NPEP as described in section 2.4 of this
appendix or a comparable program.
Performance evaluations will be performed
annually within each PQAO. For PQAOs
with less than or equal to five monitoring
sites, five valid performance evaluation
audits must be collected and reported each
year. For PQAOs with greater than five
monitoring sites, eight valid performance
evaluation audits must be collected and
reported each year. A valid performance
evaluation audit means that both the primary
monitor and PEP audit concentrations are
valid and equal to or greater than 2 mg/m3.
Siting of the PEP monitor must be consistent
with section 3.2.3.4(c) of this appendix.
However, any horizontal distance greater
than 4 meters and any vertical distance
greater than one meter must be reported to
the EPA regional PEP coordinator.
2.6.1 Gaseous pollutant concentration
standards (permeation devices or cylinders of
compressed gas) used to obtain test
concentrations for CO, SO2, NO, and NO2
must be EPA Protocol Gases certified in
accordance with one of the procedures given
in Reference 4 of this appendix.
2.6.1.1 The concentrations of EPA
Protocol Gas standards used for ambient air
monitoring must be certified with a 95percent confidence interval to have an
analytical uncertainty of no more than ±2.0
percent (inclusive) of the certified
concentration (tag value) of the gas mixture.
The uncertainty must be calculated in
accordance with the statistical procedures
defined in Reference 4 of this appendix.
2.6.1.2 Specialty gas producers
advertising certification with the procedures
provided in Reference 4 of this appendix and
distributing gases as ‘‘EPA Protocol Gas’’ for
ambient air monitoring purposes must adhere
to the regulatory requirements specified in 40
CFR 75.21(g) or not use ‘‘EPA’’ in any form
jcV90NAAQS
*
*
*
*
*
(6) List of Designated Reference and
Equivalent Methods. Available from U.S.
Environmental Protection Agency,
Center for Environmental Measurements
and Modeling, Air Methods and
Characterization Division, MD–D205–03,
E:\FR\FM\27JAP3.SGM
27JAP3
EP27JA23.016
Appendix B to Part 58—Quality
Assurance Requirements for Prevention
of Significant Deterioration (PSD) Air
Monitoring
*
*
3.1.3.3 Using audit gases that are verified
against the NIST standard reference methods
or special review procedures and validated
per the certification periods specified in
Reference 4 of this appendix (EPA
Traceability Protocol for Assay and
Certification of Gaseous Calibration
Standards) for CO, SO2, and NO2 and using
O3 analyzers that are verified quarterly
against a standard reference photometer.
EP27JA23.015
*
Additionally for every monitor designated
as a primary monitor, a primary quality
assurance organization must:
3.2.4.1 Have each method designation
evaluated each year; and,
3.2.4.2 Have all FRM, FEM, or ARM
samplers subject to a PEP audit at least once
every 6 years, which equates to
approximately 15 percent of the monitoring
sites audited each year.
3.2.4.3 Additional information
concerning the PEP is contained in Reference
10 of this appendix. The calculations for
evaluating bias between the primary monitor
and the performance evaluation monitor for
PM2.5 are described in section 4.2.5 of this
appendix.
EP27JA23.014
b. By removing and reserving section
3.1.2.2;
■ c. By revising sections 3.1.3.3 and
3.2.4;
■ d. By adding sections 3.2.4.1 through
3.2.4.3;
■ e. By revising sections 4.2.1, and
4.2.5; and
■ f. In section 6 by revising References
(1), (4), (6), (7), (9), (10), and (11) and
table B–1.
The revisions and additions read as
follows:
■
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Research Triangle Park, NC 27711.
https://www.epa.gov/amtic/airmonitoring-methods-criteria-pollutants.
(7) Transfer Standards for the Calibration of
Ambient Air Monitoring Analyzers for
Ozone. EPA–454/B–13–004 U.S.
Environmental Protection Agency,
Research Triangle Park, NC 27711,
October, 2013. https://www.epa.gov/
sites/default/files/2020–09/documents/
ozonetransferstandardguidance.pdf.
*
*
*
*
*
(9) Quality Assurance Handbook for Air
Pollution Measurement Systems, Volume
1—A Field Guide to Environmental
Quality Assurance. EPA–600/R–94/038a.
April 1994. Available from U.S.
Environmental Protection Agency, ORD
Publications Office, Center for
Environmental Research Information
(CERI), 26 W Martin Luther King Drive,
Cincinnati, OH 45268. https://
www.epa.gov/amtic/ambient-airmonitoring-qualityassurance#documents.
(10) Quality Assurance Handbook for Air
Pollution Measurement Systems, Volume
II: Ambient Air Quality Monitoring
Program Quality System Development.
EPA–454/B–13–003. https://
www.epa.gov/amtic/ambient-airmonitoring-qualityassurance#documents.
(11) National Performance Evaluation
Program Standard Operating Procedures.
https://www.epa.gov/amtic/ambient-airmonitoring-quality-assurance#npep.
TABLE B–1 TO APPENDIX B TO PART 58—MINIMUM DATA ASSESSMENT REQUIREMENTS FOR NAAQS RELATED CRITERIA
POLLUTANT PSD MONITORS
Assessment
method
Coverage
Minimum
frequency
Parameters
reported
Response check at concentration 0.005–0.08
ppm SO2, NO2, O3, &
0.5 and 5 ppm CO.
See section 3.1.2 of this
appendix.
Each analyzer .................
Once per 2 weeks 5 ........
Audit concentration 1 and
measured concentration 2.
One-Point QC.
Each analyzer .................
Once per quarter 5 ..........
Annual PE.
Independent Audit ..........
Each primary monitor .....
Once per year ................
Audit concentration 1 and
measured concentration 2 for each level.
Audit concentration 1 and
measured concentration 2 for each level.
Collocated samplers .......
1 per PSD Network per
pollutant.
Every 6 days or every 3
days if daily monitoring
required.
No Transaction reported
as raw data.
Flow rate verification
PM10, PM2.5, Pb.
Check of sampler flow
rate.
Each sampler .................
Once every month 5 ........
Semi-annual flow rate
audit PM10, PM2.5,
Pb.
Pb analysis audits
Pb-TSP, Pb-PM10.
Check of sampler flow
rate using independent
standard.
Check of analytical system with Pb audit
strips/filters.
Each sampler .................
Once every 6 months or
beginning, middle and
end of monitoring 5.
Each quarter 5 .................
Performance Evaluation Program
PM2.5 3.
Collocated samplers .......
Performance Evaluation Program Pb 3.
Collocated samplers .......
(1) 5 valid audits for
PQAOs with <5 sites.
(2) 8 valid audits for
PQAOs with >5 sites.
(3) All samplers in 6
years.
(1) 1 valid audit and 4
collocated samples for
PQAOs, with <5 sites.
(2) 2 valid audits and 6
collocated samples for
PQAOs with >5 sites.
Primary sampler concentration and duplicate sampler concentration 4.
Audit flow rate and
measured flow rate indicated by the sampler.
Audit flow rate and
measured flow rate indicated by the sampler.
Measured value and
audit value (μg Pb/filter) using AQS unit
code 077 for parameters: 14129—Pb
(TSP) LC FRM/FEM
85129—Pb (TSP) LC
Non-FRM/FEM.
Primary sampler concentration and performance evaluation sampler concentration.
Primary sampler concentration and performance evaluation sampler concentration. Primary sampler concentration and duplicate sampler concentration.
PEP.
Method
Gaseous Methods (CO,
NO2, SO2, O3):
One-Point QC for
SO2, NO2, O3, CO.
Quarterly performance evaluation for
SO2, NO2, O3, CO.
NPAP for SO2, NO2,
O3, CO3.
Particulate Methods:
Collocated sampling
PM10, PM2.5, Pb.
Analytical ........................
Over all 4 quarters 5 .......
Over all 4 quarters 5 .......
AQS
assessment type
NPAP.
Flow Rate Verification.
Semi Annual Flow Rate
Audit.
Pb Analysis Audits.
PEP.
1 Effective
concentration for open path analyzers.
concentration, if applicable for open path analyzers.
PM2.5, PEP, and Pb-PEP must be implemented if data is used for NAAQS decisions otherwise implementation is at PSD reviewing authority discretion.
4 Both primary and collocated sampler values are reported as raw data.
5 A maximum number of days should be between these checks to ensure the checks are routinely conducted over time and to limit data impacts resulting from a
failed check.
2 Corrected
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3 NPAP,
■ 28. Amend appendix C to part 58 as
follows:
■ a. By adding sections 2.2 and 2.2.1
through 2.2.19; and
■ b. By removing and reserving sections
2.4, 2.4.1, and 2.4.1.1 through 2.4.1.7.
The additions reads as follows:
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Appendix C to Part 58—Ambient Air
Quality Monitoring Methodology
*
*
*
*
*
2.2 PM10, PM2.5, or PM10–2.5 continuous
FEMs with existing valid designations may
be calibrated using network data from
collocated FRM and continuous FEM data
under the following provisions:
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2.2.1 Data to demonstrate a calibration
may include valid data from State, local, or
Tribal air agencies or data collected by
instrument manufacturers in accordance with
40 CFR 53.35 or other data approved by the
Administrator.
2.2.2 A request to update a designated
methods calibration may be initiated by the
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instrument manufacturer of record or the
EPA Administrator.
2.2.3 Requests for approval of an updated
PM10, PM2.5, or PM10–2.5 continuous FEM
calibration must meet the general submittal
requirements of section 2.7 of this appendix.
2.2.4 Data included in the request should
represent a subset of representative locations
where the method is operational. For cases
with a small number of collocated FRMs and
continuous FEMs sites, an updated candidate
calibration may be limited to the sites where
both methods are in use.
2.2.5 Data included in a candidate
method updated calibration may include a
subset of sites where there is a large grouping
of sites in one part of the country such that
the updated calibration would be
representative of the country as a whole.
2.2.6 Improvements should be national in
scope and ideally implemented through a
firmware change.
2.2.7 The goal of a change to a methods
calibration is to increase the number of sites
meeting measurements quality objectives of
the method as identified in section 2.3.1.1 of
appendix A to this part.
2.2.8 For meeting measurement quality
objectives (MQOs), the primary objective is to
meet the bias goal as this statistic will likely
have the most influence on improving the
resultant data collected.
2.2.9 Precision data are to be included,
but so long as precision data are at least as
good as existing network data or meet the
MQO referenced in section 2.2.8 of this
appendix, no further work is necessary with
precision.
2.2.10 Data available to use may include
routine primary and collocated data.
2.2.11 Audit data may be useful to
confirm the performance of a candidate
updated calibration but should not be used
as the basis of the calibration to keep the
independence of the audit data.
2.2.12 Data utilized as the basis of the
updated calibration may be obtained by
accessing EPA’s AQS database.
2.2.13 Years of data to use in a candidate
method calibration should include two
recent years where we are past the
certification period for the previous year’s
data, which is May 1st of each year.
2.2.14 Data from additional years is to be
used to test an updated calibration such that
the calibration is independent of the test
years of interest. Data from these additional
years need to minimally demonstrate that a
larger number of sites are expected to meet
bias MQO especially at sites near the level of
the NAAQS for the PM indicator of interest
2.2.15 Outliers may be excluded using
routine outlier tests.
2.2.16 The range of data used in a
calibration may include all data available or
alternatively use data in the range from the
lowest measured data available up to 125%
of the 24-hour NAAQS for the PM indicator
of interest.
2.2.17 Other improvements to a PM
continuous method may be included as part
of a recommended update so long as
appropriate testing is conducted with input
from EPA’s Office of Research and
Development (ORD) Reference and
Equivalent (R&E) Methods Designation
program.
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2.2.18 EPA encourages early
communication by instrument manufacturers
considering an update to a PM method.
Instrument companies should initiate such
dialogue by contacting EPA’s ORD R&E
Methods Designation program. The contact
information for this can be found at 40 CFR
53.4.
2.2.19 Manufacturers interested in
improving instrument’s performance through
an updated factory calibration must submit a
written modification request to EPA with
supporting rationale. Because the testing
requirements and acceptance criteria of any
field and/or lab tests can depend upon the
nature and extent of the intended
modification, applicants should contact
EPA’s R&E Methods Designation program for
guidance prior to development of the
modification request.
*
*
*
*
*
29. Amend appendix D to part 58 by
revising sections 1 and 1.1(b), the
introductory text before the table in
section 4.7.1(a), and sections 4.7.1(b)(3)
and 4.7.2 to read as follows:
■
Appendix D to Part 58—Network
Design Criteria for Ambient Air Quality
Monitoring
*
*
*
*
*
1. Monitoring Objectives and Spatial Scales
The purpose of this appendix is to describe
monitoring objectives and general criteria to
be applied in establishing the required
SLAMS ambient air quality monitoring
stations and for choosing general locations
for additional monitoring sites. This
appendix also describes specific
requirements for the number and location of
FRM and FEM sites for specific pollutants,
NCore multipollutant sites, PM10 mass sites,
PM2.5 mass sites, chemically-speciated PM2.5
sites, and O3 precursor measurements sites
(PAMS). These criteria will be used by EPA
in evaluating the adequacy of the air
pollutant monitoring networks.
1.1 * * *
(b) Support compliance with ambient air
quality standards and emissions strategy
development. Data from FRM and FEM
monitors for NAAQS pollutants will be used
for comparing an area’s air pollution levels
against the NAAQS. Data from monitors of
various types can be used in the development
of attainment and maintenance plans.
SLAMS, and especially NCore station data,
will be used to evaluate the regional air
quality models used in developing emission
strategies, and to track trends in air pollution
abatement control measures’ impact on
improving air quality. In monitoring
locations near major air pollution sources,
source-oriented monitoring data can provide
insight into how well industrial sources are
controlling their pollutant emissions.
*
*
*
*
*
4.7.1 * * *
(a) State, and where applicable local,
agencies must operate the minimum number
of required PM2.5 SLAMS sites listed in table
D–5 to this appendix. The NCore sites are
expected to complement the PM2.5 data
collection that takes place at non-NCore
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SLAMS sites, and both types of sites can be
used to meet the minimum PM2.5 network
requirements. The total number of PM2.5 sites
needed to support the basic monitoring
objectives of providing air pollution data to
the general public in a timely manner,
support compliance with ambient air quality
standards and emission strategy
development, and support for air pollution
research studies will include more sites than
the minimum numbers required in table D–
5 to this appendix. Deviations from these
PM2.5 monitoring requirements must be
approved by the EPA Regional
Administrator.
*
*
*
*
*
(b) * * *
(3) For areas with additional required
SLAMS, a monitoring station is to be sited in
an at-risk community, particularly where
there are anticipated effects from sources in
the area (e.g., a major port, rail yard, airport,
industrial area, or major transportation
corridor).
*
*
*
*
*
4.7.2 Requirement for Continuous PM2.5
Monitoring. The state, or where appropriate,
local agencies must operate continuous PM2.5
analyzers equal to at least one-half (round
up) the minimum required sites listed in
table D–5 to this appendix. At least one
required continuous analyzer in each MSA
must be collocated with one of the required
FRM/FEM monitors, unless at least one of the
required FRM/FEM monitors is itself a
continuous FEM monitor in which case no
collocation requirement applies. State and
local air monitoring agencies must use
methodologies and quality assurance/quality
control (QA/QC) procedures approved by the
EPA Regional Administrator for these
required continuous analyzers.
*
*
*
*
*
30. Revise appendix E to part 58 to
read as follows:
■
Appendix E to Part 58—Probe and
Monitoring Path Siting Criteria for
Ambient Air Quality Monitoring
1. Introduction
2. Monitors and Samplers with Probe Inlets
3. Open Path Analyzers
4. Waiver Provisions
5. References
1. Introduction
1.1 Applicability
(a) This appendix contains specific
location criteria applicable to ambient air
quality monitoring probes, inlets, and optical
paths of SLAMS, NCore, PAMS, and other
monitor types whose data are intended to be
used to determine compliance with the
NAAQS. These specific location criteria are
relevant after the general location has been
selected based on the monitoring objectives
and spatial scale of representation discussed
in appendix D to this part. Monitor probe
material and sample residence time
requirements are also included in this
appendix. Adherence to these siting criteria
is necessary to ensure the uniform collection
of compatible and comparable air quality
data.
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(b) The probe and monitoring path siting
criteria discussed in this appendix must be
followed to the maximum extent possible. It
is recognized that there may be situations
where some deviation from the siting criteria
may be necessary. In any such case, the
reasons must be thoroughly documented in a
written request for a waiver that describes
how and why the proposed siting deviates
from the criteria. This documentation should
help to avoid later questions about the
validity of the resulting monitoring data.
Conditions under which the EPA would
consider an application for waiver from these
siting criteria are discussed in section 4 of
this appendix.
(c) The pollutant-specific probe and
monitoring path siting criteria generally
apply to all spatial scales except where noted
otherwise. Specific siting criteria that are
phrased with a ‘‘must’’ are defined as
requirements and exceptions must be
approved through the waiver provisions.
However, siting criteria that are phrased with
a ‘‘should’’ are defined as goals to meet for
consistency but are not requirements.
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2. Monitors and Samplers With Probe Inlets
2.1 Horizontal and Vertical Placement
The probe must be located greater than or
equal to 2.0 and less than or equal to 15.
meters above ground level for all O3 and SO2
monitoring, and for neighborhood or larger
spatial scale Pb, PM10, PM10–2.5, PM2.5, NO2,
and CO sites. Middle scale CO and NO2
monitors must also have sampler inlets
greater than or equal to 2.0 and less than or
equal to 15 meters above ground level.
Middle scale PM10–2.5 sites are required to
have sampler inlets greater than or equal to
2.0 and less than or equal to 7.0 meters above
ground level. Microscale Pb, PM10, PM10–2.5,
and PM2.5 sites are required to have sampler
inlets greater than or equal to 2.0 and less
than or equal to 7.0 meters above ground
level. Microscale near-road NO2 monitoring
sites are required to have sampler inlets
greater than or equal to 2.0 and less than or
equal to 7.0 meters above ground level. The
probe inlets for microscale carbon monoxide
monitors that are being used to measure
concentrations near roadways must be greater
than or equal to 2.0 and less than or equal
to 7.0 meters above ground level. Those
probe inlets for microscale carbon monoxide
monitors measuring concentrations near
roadways in downtown areas or urban street
canyons must be greater than or equal to 2.5
and less than or equal to 3.5 meters above
ground level. The probe must be at least 1.0
meter vertically or horizontally away from
any supporting structure, walls, parapets,
penthouses, etc., and away from dusty or
dirty areas. If the probe is located near the
side of a building or wall, then it should be
located on the windward side of the building
relative to the prevailing wind direction
during the season of highest concentration
potential for the pollutant being measured.
2.2 Spacing From Minor Sources
(a) It is important to understand the
monitoring objective for a particular location
in order to interpret this particular
requirement. Local minor sources of a
primary pollutant, such as SO2, lead, or
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particles, can cause high concentrations of
that particular pollutant at a monitoring site.
If the objective for that monitoring site is to
investigate these local primary pollutant
emissions, then the site is likely to be
properly located nearby. This type of
monitoring site would in all likelihood be a
microscale type of monitoring site. If a
monitoring site is to be used to determine air
quality over a much larger area, such as a
neighborhood or city, a monitoring agency
should avoid placing a monitor probe inlet
near local, minor sources. The plume from
the local minor sources should not be
allowed to inappropriately impact the air
quality data collected at a site. Particulate
matter sites should not be located in an
unpaved area unless there is vegetative
ground cover year-round, so that the impact
of windblown dusts will be kept to a
minimum.
(b) Similarly, local sources of nitric oxide
(NO) and ozone-reactive hydrocarbons can
have a scavenging effect causing
unrepresentatively low concentrations of O3
in the vicinity of probes for O3. To minimize
these potential interferences the probe inlet
should be away from furnace or incineration
flues or other minor sources of SO2 or NO.
The separation distance should take into
account the heights of the flues, type of waste
or fuel burned, and the sulfur content of the
fuel.
2.3 Spacing From Obstructions
(a) Buildings and other obstacles may
possibly scavenge SO2, O3, or NO2, and can
act to restrict airflow for any pollutant. To
avoid this interference, the probe inlet must
have unrestricted airflow pursuant to
paragraph (b) of this section and should be
located away from obstacles. The horizontal
distance from the obstacle to the probe inlet
must be at least twice the height that the
obstacle protrudes above the probe inlet. An
obstacle that does not meet the minimum
distance requirement is considered an
obstruction that restricts airflow to the probe
inlet.
(b) A probe inlet located near or along a
vertical wall is undesirable because air
moving along the wall may be subject to
possible removal mechanisms. A probe inlet
must have unrestricted airflow with no
obstructions (as defined in paragraph (a) of
this section) in a continuous arc of at least
270 degrees. An unobstructed continuous arc
of 180 degrees is allowable when network
design criteria regulations specified in
appendix D to this part require monitoring in
street canyons and the probe is located on the
side of a building. This arc must include the
predominant wind direction for the season of
greatest pollutant concentration potential.
For particle sampling, a minimum of 2.0
meters of horizontal separation from walls,
parapets, and structures is required for
rooftop site placement.
(c) A sampling station having a probe inlet
located closer to an obstacle than this
criterion allows should be classified as
middle scale or microscale rather than
neighborhood or urban scale, since the
measurements from such a station would
more closely represent these smaller scales.
(d) For near-road monitoring stations, the
monitor probe shall have an unobstructed air
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flow, where no obstacles exist at or above the
height of the monitor probe, between the
monitor probe and the outside nearest edge
of the traffic lanes of the target road segment.
2.4 Spacing From Trees
(a) Trees can provide surfaces for SO2, O3,
or NO2 adsorption or reactions, and surfaces
for particle deposition. Trees can also act as
obstructions in cases where they are located
between the air pollutant sources or source
areas and the monitoring site, and where the
trees are of a sufficient height and leaf
canopy density to interfere with the normal
airflow around the probe inlet. To reduce this
possible interference/obstruction, the probe
inlet should be 20 meters or more from the
drip line of trees and must be at least 10
meters from the drip line of trees. If a tree
or trees is an obstacle, the probe inlet must
meet the distance requirements of section 2.3
of this appendix.
(b) The scavenging effect of trees is greater
for O3 than for other criteria pollutants.
Monitoring agencies must take steps to
consider the impact of trees on ozone
monitoring sites and take steps to avoid this
problem.
(c) Beginning January 1, 2024, microscale
sites of any air pollutant, shall have no trees
or shrubs located at or above the line-of-sight
fetch between the probe and the source under
investigation, such as a roadway or a
stationary source.
2.5
Spacing From Roadways
TABLE E–1 TO APPENDIX E TO PART
58—MINIMUM SEPARATION DISTANCE BETWEEN ROADWAYS AND
PROBES FOR MONITORING NEIGHBORHOOD
AND
URBAN SCALE
OZONE (O3) AND OXIDES OF NITROGEN (NO, NO2, NOX, NOy)
Roadway
average
daily traffic,
vehicles per
day
≤1,000 .......
10,000 .......
15,000 .......
20,000 .......
40,000 .......
70,000 .......
≥110,000 ...
Minimum
distance 1 3
(meters)
10
10
20
30
50
100
250
Minimum
distance 1 2 3
(meters)
10
20
30
40
60
100
250
1 Distance from the edge of the nearest traffic lane. The distance for intermediate traffic
counts should be interpolated from the table
values based on the actual traffic count.
2 Applicable
for ozone monitors whose
placement has not already been approved as
of December 18, 2006.
3 All distances listed are expressed as having 2 significant figures. When rounding is performed to assess compliance with these siting
requirements, the distance measurements will
be rounded such as to retain at least two significant figures.
2.5.1 Spacing for Ozone Probes
In siting an O3 monitor, it is important to
minimize destructive interferences from
sources of NO, since NO readily reacts with
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O3. Table E–1 to this appendix provides the
required minimum separation distances
between a roadway and a probe inlet for
various ranges of daily roadway traffic. A
sampling site having a monitor probe located
closer to a roadway than allowed by the table
E–1 requirements should be classified as
middle scale or microscale, rather than
neighborhood or urban scale, since the
measurements from such a site would more
closely represent these smaller scales.
2.5.2
Spacing for Carbon Monoxide Probes
(a) Near-road microscale CO monitoring
sites, including those located in downtown
areas, urban street canyons, and other nearroad locations such as those adjacent to
highly trafficked roads, are intended to
provide a measurement of the influence of
the immediate source on the pollution
exposure on the adjacent area.
(b) Microscale CO monitor probe inlets in
downtown areas or urban street canyon
locations shall be located a minimum
distance of 2.0 meters and a maximum
distance of 10 meters from the edge of the
nearest traffic lane.
(c) Microscale CO monitor probe inlets in
downtown areas or urban street canyon
locations shall be located at least 10 meters
from an intersection and preferably at a
midblock location. Midblock locations are
preferable to intersection locations because
intersections represent a much smaller
portion of downtown space than do the
streets between them. Pedestrian exposure is
probably also greater in street canyon/
corridors than at intersections.
TABLE E–2 TO APPENDIX E TO PART
58—MINIMUM SEPARATION DISTANCE BETWEEN ROADWAYS AND
PROBES FOR MONITORING NEIGHBORHOOD SCALE CARBON MONOXIDE
Roadway average daily
traffic, vehicles per day
Minimum
distance 1 2
(meters)
khammond on DSKJM1Z7X2PROD with PROPOSALS3
≤10,000 .................................
15,000 ...................................
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25
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TABLE E–2 TO APPENDIX E TO PART
58—MINIMUM SEPARATION DISTANCE BETWEEN ROADWAYS AND
PROBES FOR MONITORING NEIGHBORHOOD SCALE CARBON MONOXIDE—Continued
Roadway average daily
traffic, vehicles per day
20,000 ...................................
30,000 ...................................
40,000 ...................................
50,000 ...................................
≥60,000 .................................
Minimum
distance 1 2
(meters)
45
80
115
135
150
1 Distance from the edge of the nearest traffic lane. The distance for intermediate traffic
counts should be interpolated from the table
values based on the actual traffic count.
2 All distances listed are expressed as having 2 significant figures. When rounding is performed to assess compliance with these siting
requirements, the distance measurements will
be rounded such as to retain at least two significant figures.
2.5.3 Spacing for Particulate Matter (PM2.5,
PM2.5–10, PM10, Pb) Inlets
(a) Since emissions associated with the
operation of motor vehicles contribute to
urban area particulate matter ambient levels,
spacing from roadway criteria are necessary
for ensuring national consistency in PM
sampler siting.
(b) The intent is to locate localized hot-spot
sites in areas of highest concentrations
whether it be from mobile or multiple
stationary sources. If the area is primarily
affected by mobile sources and the maximum
concentration area(s) is judged to be a traffic
corridor or street canyon location, then the
monitors should be located near roadways
with the highest traffic volume and at
separation distances most likely to produce
the highest concentrations. For the
microscale traffic corridor site, the location
must be greater than or equal 5.0 and less
than or equal to 15 meters from the major
roadway. For the microscale street canyon
site, the location must be greater than or
equal 2.0 and less than or equal to 10 meters
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5711
from the roadway. For the middle scale site,
a range of acceptable distances from the
roadway is shown in figure E–1 to this
appendix. Figure E–1 also includes
separation distances between a roadway and
neighborhood or larger scale sites by default.
Any PM probe inlet at a site, 2.0 to 15 meters
high, and further back than the middle scale
requirements will generally be neighborhood,
urban or regional scale. For example,
according to figure E–1, if a PM sampler is
primarily influenced by roadway emissions
and that sampler is set back 10 meters from
a 30,000 ADT (average daily traffic) road, the
site should be classified as microscale, if the
sampler’s inlet height is between 2.0 and 7.0
meters. If the sampler’s inlet height is
between 7.0 and 15 meters, the site should
be classified as middle scale. If the sampler
is 20 meters from the same road, it will be
classified as middle scale; if 40 meters,
neighborhood scale; and if 110 meters, an
urban scale.
2.5.4 Spacing for Nitrogen Dioxide (NO2)
Probes
(a) In siting near-road NO2 monitors as
required in section 4.3.2 of appendix D to
this part, the monitor probe shall be as near
as practicable to the outside nearest edge of
the traffic lanes of the target road segment;
but shall not be located at a distance greater
than 50 meters, in the horizontal, from the
outside nearest edge of the traffic lanes of the
target road segment. Where possible, the
near-road NO2 monitor probe should be
within 20 meters of the target road segment.
(b) In siting NO2 monitors for
neighborhood and larger scale monitoring, it
is important to minimize near-road
influences. Table E–1 to this appendix
provides the required minimum separation
distances between a roadway and a probe
inlet for various ranges of daily roadway
traffic. A sampling site having a monitor
probe located closer to a roadway than
allowed by the table E–1 requirements
should be classified as microscale or middle
scale rather than neighborhood or urban
scale.
Figure E–1 to Appendix E to Part 58
E:\FR\FM\27JAP3.SGM
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100
-- ....
I
I
.iI
40"
20·
• •
0
•
40
80
100
148
120
1A
Flpn 1,-J. Dktanftof PM sampfffl to - - - b8Je taae (meters)
2.6 Probe Material and Pollutant Sampler
Residence Time
(a) For the reactive gases (SO2, NO2, and
O3), special probe material must be used for
monitors. Studies have been conducted to
determine the suitability of materials such as
polypropylene, polyethylene, polyvinyl
chloride, Tygon®, aluminum, brass, stainless
steel, copper, borosilicate glass,
polyvinylidene fluoride (PVDF),
polytetrafluoroethylene (PTFE),
perfluoroalkoxy (PFA), and fluorinated
ethylene propylene (FEP) for use as intake
sampling lines. Of the materials in the
preceding sentence, only borosilicate glass,
PVDF, PTFE, PFA, and FEP have been found
to be acceptable for use as intake sampling
lines for all the reactive gaseous pollutants.
Furthermore, the EPA has specified
borosilicate glass or FEP Teflon® as the only
acceptable probe materials for delivering test
atmospheres in the determination of
reference or equivalent methods. Therefore,
borosilicate glass, PVDF, PTFE, PFA, FEP, or
their equivalent must be the only material in
the sampling train (from probe inlet to the
back of the monitor) that can be in contact
with the ambient air sample for reactive gas
monitors. NafionTM is composed primarily of
PTFE and can be considered equivalent to
PTFE. It has been shown in tests to exhibit
virtually no loss of ozone at 20 second
residence times.
(b) For volatile organic compound (VOC)
monitoring at PAMS, FEP Teflon® is
unacceptable as the probe material because of
VOC adsorption and desorption reactions on
the FEP Teflon®. Borosilicate glass, stainless
steel, or its equivalent are the acceptable
probe materials for VOC and carbonyl
sampling. Care must be taken to ensure that
the sample residence time is kept to 20
seconds or less.
(c) No matter how nonreactive the
sampling probe material is initially, after a
period of use reactive particulate matter is
deposited on the probe walls. Therefore, the
time it takes the gas to transfer from the
probe inlet to the sampling device is also
critical. Ozone in the presence of nitrogen
oxide (NO) will show significant losses even
in the most inert probe material when the
residence time exceeds 20 seconds. Other
studies indicate that a 10 second or less
residence time is easily achievable.
Therefore, sampling probes for reactive gas
monitors (i.e., SO2, NO2, and O3) must have
a sample residence time less than 20 seconds.
2.7
Summary
Table E–3 to this appendix presents a
summary of the general requirements for
probe siting criteria with respect to distances
and heights. It is apparent from table E–3 that
different elevation distances above the
ground are shown for the various pollutants.
The discussion in this appendix for each of
the pollutants describes reasons for elevating
the monitor or probe inlet. The differences in
the specified range of heights are based on
the vertical concentration gradients. For
source oriented and near-road monitors, the
gradients in the vertical direction are very
large for the microscale, so a small range of
heights are used. The upper limit of 15
meters is specified for the consistency
between pollutants and to allow the use of
a single manifold for monitoring more than
one pollutant.
TABLE E–3 TO APPENDIX E TO PART 58—SUMMARY OF PROBE SITING CRITERIA
SO2 2 3 4 5 .............
khammond on DSKJM1Z7X2PROD with PROPOSALS3
CO 3 4 6 .................
O3 2 3 4 ..................
NO2 2 3 4 ...............
Ozone precursors
(for PAMS) 2 3 4.
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Distance from drip line
of trees to probe 8
(meters)
≥1.0 ..........................
≥10 ..............................
N/A.
≥1.0 ..........................
≥10 ..............................
2.0–15 ....................................
≥1.0 ..........................
≥10 ..............................
2.0–10 for downtown areas or
street canyon microscale;
≤50 for near-road
microscale; see Table E–2
to this appendix for middle
and neighborhood scales.
See Table E–1 to this appendix for all scales.
2.0–7.0 (micro) .......................
2.0–15 ....................................
2.0–15 (all other scales) ........
≥1.0 ..........................
≥1.0 ..........................
≥1.0 ..........................
≥10 ..............................
≥10.
≥10 ..............................
2.0–15 ....................................
≥1.0 ..........................
≥10 ..............................
Height from ground to
(meters)
Scale
Middle (300 m) Neighborhood 2.0–15 ....................................
Urban, and Regional (1 km).
Micro [downtown or street
2.5–3.5; 2.0–7.0; 2.0–15 ........
canyon sites], micro [nearroad sites], middle (300 m)
and Neighborhood (1 km).
Middle (300 m) Neighborhood, Urban, and Regional
(1 km).
Micro (Near-road [50–300 m])
Middle (300 m) .......................
Neighborhood, Urban, and
Regional (1 km).
Neighborhood and Urban (1
km).
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Distance from roadways
to probe 8
(meters)
≤50 for near-road micro-scale.
See Table E–1 to this appendix for all other scales.
See Table E–1 to this appendix for all scales.
EP27JA23.017
Pollutant
Horizontal or vertical
distance from
supporting
structures 2 8 to
probe inlet
(meters)
probe 8
Federal Register / Vol. 88, No. 18 / Friday, January 27, 2023 / Proposed Rules
5713
TABLE E–3 TO APPENDIX E TO PART 58—SUMMARY OF PROBE SITING CRITERIA—Continued
Height from ground to probe 8
(meters)
Pollutant
Scale
PM, Pb 2 3 4 7 ........
Micro, Middle, Neighborhood,
Urban and Regional.
2.0–7.0 (micro); 2.0–7.0 (middle PM10–2.5); 2.0–7.0 for
near-road; 2.0–15 (all other
scales).
Horizontal or vertical
distance from
supporting
structures 2 8 to
probe inlet
(meters)
≥2.0 (all scales, horizontal distance
only).
Distance from drip line
of trees to probe 8
(meters)
Distance from roadways
to probe 8
(meters)
≥10 (all scales) ...........
2.0–10 (micro); see Figure E–
1 to this appendix for all
other scales. ≤50 for nearroad.
N/A—Not applicable.
1 When probe is located on a rooftop, this separation distance is in reference to walls, parapets, or penthouses located on roof.
2 Should be greater than 20 meters from the dripline of tree(s) and must be 10 meters from the dripline.
3 Distance from sampler or probe inlet to obstacle, such as a building, must be at least twice the height the obstacle protrudes above the sampler or probe inlet.
Sites not meeting this criterion may be classified as microscale or middle scale (see text).
4 Must have unrestricted airflow in a continuous arc of at least 270 degrees around the probe or sampler; 180 degrees if the probe is on the side of a building or a
wall for street canyon monitoring.
5 The probe or sampler should be away from minor sources, such as furnace or incineration flues. The separation distance is dependent on the height of the minor
source’s emission point (such as a flue), the type of fuel or waste burned, and the quality of the fuel (sulfur, ash, or lead content). This criterion is designed to avoid
undue influences from minor sources.
6 For microscale CO monitoring sites, the probe must be ≥10 meters from a street intersection and preferably at a midblock location.
7 Collocated monitor inlets must be within 4.0 meters of each other and at least 2.0 meters apart for flow rates greater than 200 liters/min or at least 1.0 meter apart
for samplers having flow rates less than 200 liters/min to preclude airflow interference, unless a waiver is in place as approved by the Regional Administrator pursuant
to section 3 of appendix A to this part. For PM2.5, collocated monitor inlet heights should be within 1 meter of each other vertically.
8 All distances listed are expressed as having 2 significant figures. When rounding is performed to assess compliance with these siting requirements, the distance
measurements will be rounded such as to retain at least two significant figures.
3. Open Path Analyzers
khammond on DSKJM1Z7X2PROD with PROPOSALS3
3.1 Horizontal and Vertical Placement
At least 80 percent of the monitoring path,
must be located greater than or equal 2.0 and
less than or equal to 15 meters above ground
level for all O3 and SO2 monitoring sites, and
for neighborhood or larger spatial scale NO2,
and CO sites. Middle scale CO and NO2 sites
must also have monitoring paths greater than
or equal 2.0 and less than or equal to 15
meters above ground level. Microscale nearroad monitoring sites are required to have
monitoring paths greater than or equal 2.0
and less than or equal to 7.0 meters above
ground level. The monitoring path for
microscale carbon monoxide monitors that
are being used to measure concentrations
near roadways must be greater than or equal
2.0 and less than or equal to 7.0 meters above
ground level. Those monitoring paths for
microscale carbon monoxide monitors
measuring concentrations near roadways in
downtown areas or urban street canyons
must be greater than or equal 2.5 and less
than or equal to 3.5 meters above ground
level. At least 90 percent of the monitoring
path must be at least 1.0 meter vertically or
horizontally away from any supporting
structure, walls, parapets, penthouses, etc.,
and away from dusty or dirty areas. If a
significant portion of the monitoring path is
located near the side of a building or wall,
then it should be located on the windward
side of the building relative to the prevailing
wind direction during the season of highest
concentration potential for the pollutant
being measured.
3.2 Spacing From Minor Sources
(a) It is important to understand the
monitoring objective for a particular location
in order to interpret this particular
requirement. Local minor sources of a
primary pollutant, such as SO2 can cause
high concentrations of that particular
pollutant at a monitoring site. If the objective
for that monitoring site is to investigate these
local primary pollutant emissions, then the
site is likely to be properly located nearby.
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This type of monitoring site would in all
likelihood be a microscale type of monitoring
site. If a monitoring site is to be used to
determine air quality over a much larger area,
such as a neighborhood or city, a monitoring
agency should avoid placing a monitoring
path near local, minor sources. The plume
from the local minor sources should not be
allowed to inappropriately impact the air
quality data collected at a site.
(b) Similarly, local sources of nitric oxide
(NO) and ozone-reactive hydrocarbons can
have a scavenging effect causing
unrepresentatively low concentrations of O3
in the vicinity of monitoring paths for O3. To
minimize these potential interferences, at
least 90 percent of the monitoring path must
be away from furnace or incineration flues or
other minor sources of SO2 or NO. The
separation distance should take into account
the heights of the flues, type of waste or fuel
burned, and the sulfur content of the fuel.
3.3 Spacing From Obstructions
(a) Buildings and other obstacles may
possibly scavenge SO2, O3, or NO2, and can
act to restrict airflow for any pollutant. To
avoid this interference, at least 90 percent of
the monitoring path must have unrestricted
airflow and should be located away from
obstacles. The horizontal distance from the
obstacle to the monitoring path must be at
least twice the height that the obstacle
protrudes above the monitoring path. An
obstacle that does not meet the minimum
distance requirement is considered an
obstruction that restricts airflow to the
monitoring path.
(b) A monitoring path located near or along
a vertical wall is undesirable because air
moving along the wall may be subject to
possible removal mechanisms. At least 90
percent of the monitoring path for open path
analyzers must have unrestricted airflow
with no obstructions (as defined in paragraph
(a) of this section) in a continuous arc of at
least 270 degrees. An unobstructed
continuous arc of 180 degrees is allowable
when network design criteria regulations
specified in appendix D to this part require
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monitoring in street canyons and the
monitoring path is located on the side of a
building. This arc must include the
predominant wind direction for the season of
greatest pollutant concentration potential.
(c) Special consideration must be given to
the use of open path analyzers due to their
inherent potential sensitivity to certain types
of interferences, or optical obstructions. A
monitoring path must be clear of all trees,
brush, buildings, plumes, dust, or other
optical obstructions, including potential
obstructions that may move due to wind,
human activity, growth of vegetation, etc.
Temporary optical obstructions, such as rain,
particles, fog, or snow, should be considered
when siting an open path analyzer. Any of
these temporary obstructions that are of
sufficient density to obscure the light beam
will affect the ability of the open path
analyzer to continuously measure pollutant
concentrations. Transient, but significant
obscuration of especially longer
measurement paths could occur as a result of
certain meteorological conditions (e.g., heavy
fog, rain, snow) and/or aerosol levels that are
of a sufficient density to prevent the open
path analyzer’s light transmission. If certain
compensating measures are not otherwise
implemented at the onset of monitoring (e.g.,
shorter path lengths, higher light source
intensity), data recovery during periods of
greatest primary pollutant potential could be
compromised. For instance, if heavy fog or
high particulate levels are coincident with
periods of projected NAAQS-threatening
pollutant potential, the representativeness of
the resulting data record in reflecting
maximum pollutant concentrations may be
substantially impaired despite the fact that
the site may otherwise exhibit an acceptable,
even exceedingly high overall valid data
capture rate.
(d) A sampling station having a monitoring
path located closer to an obstacle than this
criterion allows should be classified as
middle scale or microscale rather than
neighborhood or urban scale, since the
measurements from such a station would
more closely represent these smaller scales.
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(e) For near-road monitoring stations, the
monitoring path shall have an unobstructed
air flow, where no obstacles exist at or above
the height of the monitoring path, between
the monitoring path and the outside nearest
edge of the traffic lanes of the target road
segment.
3.4 Spacing From Trees
(a) Trees can provide surfaces for SO2, O3,
or NO2 adsorption or reactions. Trees can
also act as obstructions in cases where they
are located between the air pollutant sources
or source areas and the monitoring site, and
where the trees are of a sufficient height and
leaf canopy density to interfere with the
normal airflow around the monitoring path.
To reduce this possible interference/
obstruction, at least 90 percent of the
monitoring path should be 20 meters or more
from the drip line of trees and must be at
least 10 meters from the drip line of trees. If
a tree or trees could be considered an
obstacle, the monitoring path must meet the
distance requirements of section 3.3 of this
appendix.
(b) The scavenging effect of trees is greater
for O3 than for other criteria pollutants.
Monitoring agencies must take steps to
consider the impact of trees on ozone
monitoring sites and take steps to avoid this
problem.
(c) Beginning January 1, 2024, microscale
sites of any air pollutant shall have no trees
or shrubs located at or above the line-of-sight
fetch between the monitoring path and the
source under investigation, such as a
roadway or a stationary source.
3.5
Spacing From Roadways
TABLE E–4 TO APPENDIX E TO PART 58—MINIMUM SEPARATION DISTANCE BETWEEN ROADWAYS AND MONITORING
PATHS FOR MONITORING NEIGHBORHOOD AND URBAN SCALE OZONE (O3) AND OXIDES OF NITROGEN (NO, NO2,
NOX, NOy)
Minimum
distance 1 3
(meters)
Roadway average daily traffic, vehicles per day
≤1,000 ..............................................................................................................................................................
10,000 ..............................................................................................................................................................
15,000 ..............................................................................................................................................................
20,000 ..............................................................................................................................................................
40,000 ..............................................................................................................................................................
70,000 ..............................................................................................................................................................
≥110,000 ..........................................................................................................................................................
Minimum
distance 1 2 3
(meters)
10
10
20
30
50
100
250
10
20
30
40
60
100
250
1 Distance from the edge of the nearest traffic lane. The distance for intermediate traffic counts should be interpolated from the table values
based on the actual traffic count.
2 Applicable for ozone open path monitors whose placement has not already been approved as of December 18, 2006.
3 All distances listed are expressed as having 2 significant figures. When rounding is performed to assess compliance with these siting requirements, the distance measurements will be rounded such as to retain at least two significant figures.
3.5.1
Spacing for Ozone Monitoring Paths
In siting an O3 open path analyzer, it is
important to minimize destructive
interferences form sources of NO, since NO
readily reacts with O3. Table E–4 to this
appendix provides the required minimum
separation distances between a roadway and
at least 90 percent of a monitoring path for
various ranges of daily roadway traffic. A
monitoring site having a monitoring path
located closer to a roadway than allowed by
the table E–4 requirements should be
classified as microscale or middle scale,
rather than neighborhood or urban scale,
since the measurements from such a site
would more closely represent these smaller
scales. The monitoring path(s) must not cross
over a roadway with an average daily traffic
count of 10,000 vehicles per day or more. For
those situations where a monitoring path
crosses a roadway with fewer than 10,000
vehicles per day, monitoring agencies must
consider the entire segment of the monitoring
path in the area of potential atmospheric
interference from automobile emissions.
Therefore, this calculation must include the
length of the monitoring path over the
roadway plus any segments of the monitoring
path that lie in the area between the roadway
and minimum separation distance, as
determined from table E–4. The sum of these
distances must not be greater than 10 percent
of the total monitoring path length.
3.5.2 Spacing for Carbon Monoxide
Monitoring Paths
(a) Near-road microscale CO monitoring
sites, including those located in downtown
areas, urban street canyons, and other nearroad locations such as those adjacent to
highly trafficked roads, are intended to
provide a measurement of the influence of
the immediate source on the pollution
exposure on the adjacent area.
(b) Microscale CO monitoring paths in
downtown areas or urban street canyon
locations shall be located a minimum
distance of 2.0 meters and a maximum
distance of 10 meters from the edge of the
nearest traffic lane.
(c) Microscale CO monitoring paths in
downtown areas or urban street canyon
locations shall be located at least 10 meters
from an intersection and preferably at a
midblock location. Midblock locations are
preferable to intersection locations because
intersections represent a much smaller
portion of downtown space than do the
streets between them. Pedestrian exposure is
probably also greater in street canyon/
corridors than at intersections.
TABLE E–5 TO APPENDIX E TO PART 58—MINIMUM SEPARATION DISTANCE BETWEEN ROADWAYS AND MONITORING
PATHS FOR MONITORING NEIGHBORHOOD SCALE CARBON MONOXIDE
Minimum distance 1 2
(meters)
khammond on DSKJM1Z7X2PROD with PROPOSALS3
Roadway average daily traffic, vehicles per day
≤10,000 ................................................................................................................................................................................
15,000 ..................................................................................................................................................................................
20,000 ..................................................................................................................................................................................
30,000 ..................................................................................................................................................................................
40,000 ..................................................................................................................................................................................
50,000 ..................................................................................................................................................................................
≥60,000 ................................................................................................................................................................................
10
25
45
80
115
135
150
1 Distance from the edge of the nearest traffic lane. The distance for intermediate traffic counts should be interpolated from the table values
based on the actual traffic count.
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5715
2 All distances listed are expressed as having 2 significant figures. When rounding is performed to assess compliance with these siting requirements, the distance measurements will be rounded such as to retain at least two significant figures.
3.5.3 Spacing for Nitrogen Dioxide (NO2)
Monitoring Paths
(a) In siting near-road NO2 monitors as
required in section 4.3.2 of appendix D to
this part, the monitoring path shall be as near
as practicable to the outside nearest edge of
the traffic lanes of the target road segment;
but shall not be located at a distance greater
than 50 meters, in the horizontal, from the
outside nearest edge of the traffic lanes of the
target road segment.
(b) In siting NO2 open path monitors for
neighborhood and larger scale monitoring, it
is important to minimize near-road
influences. Table E–5 to this appendix
provides the required minimum separation
distances between a roadway and at least 90
percent of a monitoring path for various
ranges of daily roadway traffic. An open path
analyzer having a monitoring path located
closer to a roadway than allowed by the
requirements in table E–4 to this appendix
should be classified as microscale or middle
scale rather than neighborhood or urban
scale. The monitoring path(s) must not cross
over a roadway with an average daily traffic
count of 10,000 vehicles per day or more. For
those situations where a monitoring path
crosses a roadway with fewer than 10,000
vehicles per day, monitoring agencies must
consider the entire segment of the monitoring
path in the area of potential atmospheric
interference form automobile emissions.
Therefore, this calculation must include the
length of the monitoring path over the
roadway plus any segments of the monitoring
path that lie in the area between the roadway
and minimum separation distance, as
determined form table E–5. The sum of these
distances must not be greater than 10 percent
of the total monitoring path length.
lengths may be needed in order to ensure that
the monitoring site meets the objectives and
spatial scales defined in appendix D to this
part. The Regional Administrator may require
shorter path lengths, as needed on an
individual basis, to ensure that the SLAMS
sites meet the appendix D requirements.
Likewise, the Administrator may specify the
maximum path length used at NCore
monitoring sites.
3.6 Cumulative Interferences on a
Monitoring Path
The cumulative length or portion of a
monitoring path that is affected by minor
sources, trees, or roadways must not exceed
10 percent of the total monitoring path
length.
3.8
3.7 Maximum Monitoring Path Length
The monitoring path length must not
exceed 1 kilometer for open path analyzers
in neighborhood, urban, or regional scale. For
middle scale monitoring sites, the monitoring
path length must not exceed 300 meters. In
areas subject to frequent periods of dust, fog,
rain, or snow, consideration should be given
to a shortened monitoring path length to
minimize loss of monitoring data due to
these temporary optical obstructions. For
certain ambient air monitoring scenarios
using open path analyzers, shorter path
Summary
Table E–6 to this appendix presents a
summary of the general requirements for
monitoring path siting criteria with respect to
distances and heights. It is apparent from
table E–6 that different elevation distances
above the ground are shown for the various
pollutants. The discussion in this appendix
for each of the pollutants describes reasons
for elevating the monitoring path. The
differences in the specified range of heights
are based on the vertical concentration
gradients. For source oriented and near-road
monitors, the gradients in the vertical
direction are very large for the microscale, so
a small range of heights are used. The upper
limit of 15 meters is specified for the
consistency between pollutants and to allow
the use of a monitoring path for monitoring
more than one pollutant.
TABLE E–6 TO APPENDIX E TO PART 58—SUMMARY OF MONITORING PATH SITING CRITERIA
Pollutant
Maximum monitoring path length
SO2 3 4 5 6 ............
Middle (300 m) Neighborhood
Urban, and Regional (1 km).
Micro [downtown or street canyon
sites], micro [near-road sites],
middle (300. m) and Neighborhood (1.0 km).
Middle (300. m) Neighborhood,
Urban, and Regional (1.0 km).
Micro (Near-road [50–300 m]) ........
Middle (300 m) ...............................
Neighborhood, Urban, and Regional (1 km).
Neighborhood and Urban (1 km) ...
CO 4 5 7
...............
O3 3 4 5 ................
NO2
345
..............
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Ozone precursors
(for PAMS) 3 4 5.
Height from
ground to 80% of
monitoring
path 1 8
(meters)
Horizontal or
vertical
distance from
supporting
structures 2
to 90% of
monitoring
path 1 8
(meters)
Distance from
trees to 90%
of monitoring
path 1 8
(meters)
Distance from roadways to monitoring path 1 8
(meters)
2.0–15 ................
≥1.0
≥10
N/A.
2.5–3.5; 2.0–7.0;
2.0–15.
≥1.0
≥10
2.0–15 ................
≥1.0
≥10
2.0–10 for downtown areas or street canyon
microscale; ≤50. for near-road microscale; see
Table E–5 to this appendix for middle and neighborhood scales.
See Table E–4 to this appendix for all scales.
2.0–7.0 (micro); ..
2.0–15 ................
2.0–15 (all other
scales).
2.0–15 ................
≥1.0
≥1.0
≥1.0
≥10
≥10
≥10
See Table E–4 to this appendix for all other scales.
≥1.0
≥10
See Table E–4 to this appendix for all scales.
≤50. for near-road micro-scale.
N/A—Not applicable.
1 Monitoring path for open path analyzers is applicable only to middle or neighborhood scale CO monitoring, middle, neighborhood, urban, and regional scale NO
2
monitoring, and all applicable scales for monitoring SO2, O3, and O3 precursors.
2 When the monitoring path is located on a rooftop, this separation distance is in reference to walls, parapets, or penthouses located on roof.
3 At least 90 percent of the monitoring path should be greater than 20 meters from the dripline of tree(s) and must be 10 meters from the dripline when the tree(s).
4 Distance from 90 percent of monitoring path to obstacle, such as a building, must be at least twice the height the obstacle protrudes above the monitoring path.
Sites not meeting this criterion may be classified as microscale or middle scale (see text).
5 Must have unrestricted airflow 270 degrees around at least 90 percent of the monitoring path; 180 degrees if the monitoring path is adjacent to the side of a building or a wall for street canyon monitoring.
6 The monitoring path should be away from minor sources, such as furnace or incineration flues. The separation distance is dependent on the height of the minor
source’s emission point (such as a flue), the type of fuel or waste burned, and the quality of the fuel (sulfur, ash, or lead content). This criterion is designed to avoid
undue influences from minor sources.
7 For microscale CO monitoring sites, the monitoring path must be ≥10. meters from a street intersection and preferably at a midblock location.
8 All distances listed are expressed as having 2 significant figures. When rounding is performed to assess compliance with these siting requirements, the distance
measurements will be rounded such as to retain at least two significant figures.
4. Waiver Provisions
Most sampling probes or monitors can be
located so that they meet the requirements of
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this appendix. New sites with rare
exceptions, can be located within the limits
of this appendix. However, some existing
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sites may not meet these requirements and
still produce useful data for some purposes.
The EPA will consider a written request from
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the State, or where applicable local, agency
to waive one or more siting criteria for some
monitoring sites providing that the State or
their designee can adequately demonstrate
the need (purpose) for monitoring or
establishing a monitoring site at that location.
4.1 For establishing a new site, a waiver
may be granted only if both of the following
criteria are met:
4.1.1 The site can be demonstrated to be
as representative of the monitoring area as it
would be if the siting criteria were being met.
4.1.2 The monitor or probe cannot
reasonably be located so as to meet the siting
criteria because of physical constraints (e.g.,
inability to locate the required type of site the
necessary distance from roadways or
obstructions).
4.2 However, for an existing site, a waiver
may be granted if either of the criteria in
sections 4.1.1 and 4.1.2 of this appendix are
met.
4.3 Cost benefits, historical trends, and
other factors may be used to add support to
the criteria in sections 4.1.1 and 4.1.2 of this
appendix, however, they in themselves, will
not be acceptable reasons for granting a
waiver. Written requests for waivers must be
submitted to the Regional Administrator.
Approved waivers must be renewed
minimally every 5 years and ideally as part
of the annual monitoring network plan
accompanying the network assessment as
defined in § 58.10(d). The approval date of
the waiver must be documented in the
annual monitoring network plan to support
the requirements of § 58.10(a)(1) and (b)(10).
5. References
1. Bryan, R.J., R.J. Gordon, and H. Menck.
Comparison of High Volume Air Filter
Samples at Varying Distances from Los
Angeles Freeway. University of Southern
California, School of Medicine, Los
Angeles, CA. (Presented at 66th Annual
Meeting of Air Pollution Control
Association. Chicago, IL. June 24–28,
1973. APCA 73–158.)
2. Teer, E.H. Atmospheric Lead
Concentration Above an Urban Street.
Master of Science Thesis, Washington
University, St. Louis, MO. January 1971.
3. Bradway, R.M., F.A. Record, and W.E.
Belanger. Monitoring and Modeling of
Resuspended Roadway Dust Near Urban
Arterials. GCA Technology Division,
Bedford, MA. (Presented at 1978 Annual
Meeting of Transportation Research
Board, Washington, DC. January 1978.)
4. Pace, T.G., W.P. Freas, and E.M. Afify.
Quantification of Relationship Between
Monitor Height and Measured
Particulate Levels in Seven U.S. Urban
Areas. U.S. Environmental Protection
Agency, Research Triangle Park, NC.
(Presented at 70th Annual Meeting of Air
Pollution Control Association, Toronto,
Canada. June 20–24, 1977. APCA 77–
13.4.)
5. Harrison, P.R. Considerations for Siting Air
Quality Monitors in Urban Areas. City of
Chicago, Department of Environmental
Control, Chicago, IL. (Presented at 66th
Annual Meeting of Air Pollution Control
Association, Chicago, IL. June 24–28,
1973. APCA 73–161.)
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6. Study of Suspended Particulate
Measurements at Varying Heights Above
Ground. Texas State Department of
Health, Air Control Section, Austin, TX.
1970. p.7.
7. Rodes, C.E. and G.F. Evans. Summary of
LACS Integrated Pollutant Data. In: Los
Angeles Catalyst Study Symposium. U.S.
Environmental Protection Agency,
Research Triangle Park, NC. EPA
Publication No. EPA–600/4–77–034.
June 1977.
8. Lynn, D.A. et al. National Assessment of
the Urban Particulate Problem: Volume
1, National Assessment. GCA
Technology Division, Bedford, MA. U.S.
Environmental Protection Agency,
Research Triangle Park, NC. EPA
Publication No. EPA–450/3–75–024.
June 1976.
9. Pace, T.G. Impact of Vehicle-Related
Particulates on TSP Concentrations and
Rationale for Siting Hi-Vols in the
Vicinity of Roadways. OAQPS, U.S.
Environmental Protection Agency,
Research Triangle Park, NC. April 1978.
10. Ludwig, F.L., J.H. Kealoha, and E. Shelar.
Selecting Sites for Monitoring Total
Suspended Particulates. Stanford
Research Institute, Menlo Park, CA.
Prepared for U.S. Environmental
Protection Agency, Research Triangle
Park, NC. EPA Publication No. EPA–450/
3–77–018. June 1977, revised December
1977.
11. Ball, R.J. and G.E. Anderson. Optimum
Site Exposure Criteria for SO2
Monitoring. The Center for the
Environment and Man, Inc., Hartford,
CT. Prepared for U.S. Environmental
Protection Agency, Research Triangle
Park, NC. EPA Publication No. EPA–450/
3–77–013. April 1977.
12. Ludwig, F.L. and J.H.S. Kealoha.
Selecting Sites for Carbon Monoxide
Monitoring. Stanford Research Institute,
Menlo Park, CA. Prepared for U.S.
Environmental Protection Agency,
Research Triangle Park, NC. EPA
Publication No. EPA–450/3–75–077.
September 1975.
13. Ludwig, F.L. and E. Shelar. Site Selection
for the Monitoring of Photochemical Air
Pollutants. Stanford Research Institute,
Menlo Park, CA. Prepared for U.S.
Environmental Protection Agency,
Research Triangle Park, NC. EPA
Publication No. EPA–450/3–78–013.
April 1978.
14. Lead Analysis for Kansas City and
Cincinnati, PEDCo Environmental, Inc.,
Cincinnati, OH. Prepared for U.S.
Environmental Protection Agency,
Research Triangle Park, NC. EPA
Contract No. 66–02–2515, June 1977.
15. Barltrap, D. and C.D. Strelow. Westway
Nursery Testing Project. Report to the
Greater London Council. August 1976.
16. Daines, R.H., H. Moto, and D.M. Chilko.
Atmospheric Lead: Its Relationship to
Traffic Volume and Proximity to
Highways. Environ. Sci. and Technol.,
4:318, 1970.
17. Johnson, D.E., et al. Epidemiologic Study
of the Effects of Automobile Traffic on
Blood Lead Levels, Southwest Research
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Institute, Houston, TX. Prepared for U.S.
Environmental Protection Agency,
Research Triangle Park, NC. EPA–600/1–
78–055, August 1978.
18. Air Quality Criteria for Lead. Office of
Research and Development, U.S.
Environmental Protection Agency,
Washington, DC EPA–600/8–83–028 aF–
dF, 1986, and supplements EPA–600/8–
89/049F, August 1990. (NTIS document
numbers PB87–142378 and PB91–
138420).
19. Lyman, D.R. The Atmospheric Diffusion
of Carbon Monoxide and Lead from an
Expressway, Ph.D. Dissertation,
University of Cincinnati, Cincinnati, OH.
1972.
20. Wechter, S.G. Preparation of Stable
Pollutant Gas Standards Using Treated
Aluminum Cylinders. ASTM STP.
598:40–54, 1976.
21. Wohlers, H.C., H. Newstein and D.
Daunis. Carbon Monoxide and Sulfur
Dioxide Adsorption On and Description
From Glass, Plastic and Metal Tubings.
J. Air Poll. Con. Assoc. 17:753, 1976.
22. Elfers, L.A. Field Operating Guide for
Automated Air Monitoring Equipment.
U.S. NTIS. p. 202, 249, 1971.
23. Hughes, E.E. Development of Standard
Reference Material for Air Quality
Measurement. ISA Transactions, 14:281–
291, 1975.
24. Altshuller, A.D. and A.G. Wartburg. The
Interaction of Ozone with Plastic and
Metallic Materials in a Dynamic Flow
System. Intern. Jour. Air and Water Poll.,
4:70–78, 1961.
25. Code of Federal Regulations. 40 CFR
53.22, July 1976.
26. Butcher, S.S. and R.E. Ruff. Effect of Inlet
Residence Time on Analysis of
Atmospheric Nitrogen Oxides and
Ozone, Anal. Chem., 43:1890, 1971.
27. Slowik, A.A. and E.B. Sansone. Diffusion
Losses of Sulfur Dioxide in Sampling
Manifolds. J. Air. Poll. Con. Assoc.,
24:245, 1974.
28. Yamada, V.M. and R.J. Charlson. Proper
Sizing of the Sampling Inlet Line for a
Continuous Air Monitoring Station.
Environ. Sci. and Technol., 3:483, 1969.
29. Koch, R.C. and H.E. Rector. Optimum
Network Design and Site Exposure
Criteria for Particulate Matter, GEOMET
Technologies, Inc., Rockville, MD.
Prepared for U.S. Environmental
Protection Agency, Research Triangle
Park, NC. EPA Contract No. 68–02–3584.
EPA 450/4–87–009. May 1987.
30. Burton, R.M. and J.C. Suggs. Philadelphia
Roadway Study. Environmental
Monitoring Systems Laboratory, U.S.
Environmental Protection Agency,
Research Triangle Park, N.C. EPA–600/
4–84–070 September 1984.
31. Technical Assistance Document For
Sampling and Analysis of Ozone
Precursors. Atmospheric Research and
Exposure Assessment Laboratory, U.S.
Environmental Protection Agency,
Research Triangle Park, NC 27711. EPA
600/8–91–215. October 1991.
32. Quality Assurance Handbook for Air
Pollution Measurement Systems: Volume
IV. Meteorological Measurements.
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Atmospheric Research and Exposure
Assessment Laboratory, U.S.
Environmental Protection Agency,
Research Triangle Park, NC 27711. EPA
600/4–90–0003. August 1989.
33. On-Site Meteorological Program
Guidance for Regulatory Modeling
Applications. Office of Air Quality
Planning and Standards, U.S.
Environmental Protection Agency,
Research Triangle Park, NC 27711. EPA
450/4–87–013. June 1987F.
31. Revise appendix G to part 58 to
read as follows:
■
Appendix G to Part 58—Uniform Air
Quality Index (AQI) and Daily
Reporting
3. Data Handling
1. General Information
1.1 AQI Overview. The AQI is a tool that
simplifies reporting air quality to the general
public in a nationally uniform and easy to
understand manner. The AQI converts
concentrations of pollutants for which the
EPA has established national ambient air
quality standard (NAAQS), into a uniform
scale from 0–500. These pollutants are ozone
(O3), particulate matter (PM2.5, PM10), carbon
monoxide (CO), sulfur dioxide (SO2), and
nitrogen dioxide (NO2). The scale of the
index is divided into general categories that
are associated with health messages.
2. Reporting Requirements
2.1 Applicability. The AQI must be
reported daily for a metropolitan statistical
1. General Information
2. Reporting Requirements
5717
area (MSA) with a population over 350,000.
When it is useful and possible, it is
recommended, but not required for an area to
report a sub-daily AQI as well.
2.2 Contents of AQI Report.
2.2.1 Content of AQI Report
Requirements. An AQI report must contain
the following:
a. The reporting area(s) (the MSA or
subdivision of the MSA).
b. The reporting period (the day for which
the AQI is reported).
c. The main pollutant (the pollutant with
the highest index value).
d. The AQI (the highest index value).
e. The category descriptor and index value
associated with the AQI and, if choosing to
report in a color format, the associated color.
Use only the following descriptors and colors
for the six AQI categories:
TABLE 1 TO APPENDIX G TO PART 58—AQI CATEGORIES
For this AQI
Use this descriptor
0 to 50 .........................................................................................
51 to 100 .....................................................................................
101 to 150 ...................................................................................
151 to 200 ...................................................................................
201 to 300 ...................................................................................
301 and above ............................................................................
‘‘Good’’ ......................................................................................
‘‘Moderate’’ ................................................................................
‘‘Unhealthy for Sensitive Groups’’ .............................................
‘‘Unhealthy’’ ...............................................................................
‘‘Very Unhealthy’’ ......................................................................
‘‘Hazardous’’ ..............................................................................
And this color 1
Green.
Yellow.
Orange.
Red.
Purple.
Maroon.1
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1 Specific color definitions can be found in the most recent reporting guidance (Technical Assistance Document for the Reporting of Daily Air
Quality), which can be found at https://www.airnow.gov/publications/air-quality-index/technical-assistance-document-for-reporting-the-daily-aqi/.
f. The pollutant specific sensitive groups
for any reported index value greater than 100.
The sensitive groups for each pollutant are
identified as part of the periodic review of
the air quality criteria and the NAAQS. For
convenience, EPA lists the relevant groups
for each pollutant in the most recent
reporting guidance (Technical Assistance
Document for the Reporting of Daily Air
Quality), which can be found at https://
www.airnow.gov/publications/air-qualityindex/technical-assistance-document-forreporting-the-daily-aqi/.
2.2.2 Contents of AQI Report When
Applicable. When appropriate, the AQI
report may also contain the following, but
such information is not required:
a. Appropriate health and cautionary
statements.
b. The name and index value for other
pollutants, particularly those with an index
value greater than 100.
c. The index values for sub-areas of your
MSA.
d. Causes for unusually high AQI values.
e. Pollutant concentrations.
f. Generally, the AQI report applies to an
area’s MSA only. However, if a significant air
quality problem exists (AQI greater than 100)
in areas significantly impacted by the MSA
but not in it (for example, O3 concentrations
are often highest downwind and outside an
urban area), the report should identify these
areas and report the AQI for these areas as
well.
2.3 Communication, Timing, and
Frequency of AQI Report. The daily AQI
must be reported 7 days per week and made
available via website or other means of
public access. The daily AQI report
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represents the air quality for the previous
day. Exceptions to this requirement are in
section 2.4 of this appendix.
Reporting the AQI sub-daily is
recommended, but not required, to provide
more timely air quality information to the
public for making health-protective
decisions.
Submitting hourly data in real-time to the
EPA’s AirNow (or future analogous) system
is recommended, but not required, and
assists the EPA in providing timely air
quality information to the public for making
health-protective decisions.
Submitting hourly data for appropriate
monitors (referenced in section 3.2 of this
appendix) satisfies the daily AQI reporting
requirement because the AirNow system
makes daily and sub-daily AQI reports
widely available through its website and
other communication tools.
Forecasting the daily AQI provides timely
air quality information to the public and is
recommended but not required. Sub-daily
forecasts are also recommended, especially
when air quality is expected to vary
substantially throughout the day, like during
wildfires. Long-term (multi-day) forecasts can
also be made available when useful.
2.4 Exceptions to Reporting
Requirements.
i. If the index value for a particular
pollutant remains below 50 for a season or
year, then it may be excluded from the
calculation of the AQI in section 3 of this
appendix.
ii. If all index values remain below 50 for
a year, then the AQI may be reported at the
discretion of the reporting agency. In
subsequent years, if pollutant levels rise to
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where the AQI would be above 50, then the
AQI must be reported as required in section
2 of this appendix.
iii. As previously mentioned in section 2.3
of this appendix, submitting hourly data in
real-time from appropriate monitors
(referenced in section 3.2 of this appendix)
to the EPA’s AirNow (or future analogous)
system satisfies the daily AQI reporting
requirement.
3. Data Handling
3.1 Relationship of AQI and pollutant
concentrations. For each pollutant, the AQI
transforms ambient concentrations to a scale
from 0 to 500. As appropriate, the AQI is
associated with the NAAQS for each
pollutant. In most cases, the index value of
100 is associated with the numerical level of
the short-term standard (i.e., averaging time
of 24-hours or less) for each pollutant. The
index value of 50 is associated with the
numerical level of the annual standard for a
pollutant, if there is one, at one-half the level
of the short-term standard for the pollutant,
or at the level at which it is appropriate to
begin to provide guidance on cautionary
language. Higher categories of the index are
based on the potential for increasingly
serious health effects to occur following
exposure and increasing proportions of the
population that are likely to be affected. The
reported AQI corresponds to the pollutant
with the highest calculated AQI. For the
purposes of reporting the AQI, the subindexes for PM10 and PM2.5 are to be
considered separately. The pollutant
responsible for the highest index value (the
reported AQI) is called the ‘‘main’’ pollutant
for that day.
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3.2 Monitors Used for AQI Reporting.
Concentration data from State/Local Air
Monitoring Station (SLAMS) or parts of the
SLAMS required by 40 CFR 58.10 must be
used for each pollutant except PM. For PM,
calculate and report the AQI on days for
which air quality data has been measured
(e.g., from continuous PM2.5 monitors
required in appendix D to this part). PM
measurements may be used from monitors
that are not reference or equivalent methods
(for example, continuous PM10 or PM2.5
monitors). Detailed guidance for relating nonapproved measurements to approved
methods by statistical linear regression is
referenced here:
Reference for relating non-approved PM
measurements to approved methods (Eberly,
S., T. Fitz-Simons, T. Hanley, L. Weinstock.,
T. Tamanini, G. Denniston, B. Lambeth, E.
Michel, S. Bortnick. Data Quality Objectives
(DQOs) For Relating Federal Reference
Method (FRM) and Continuous PM2.5
Measurements to Report an Air Quality Index
(AQI). U.S. Environmental Protection
Agency, Research Triangle Park, NC. EPA–
454/B–02–002, November 2002).
3.3 AQI Forecast. The AQI can be
forecasted at least 24-hours in advance using
the most accurate and reasonable procedures
considering meteorology, topography,
availability of data, and forecasting expertise.
The guidance document, ‘‘Guidelines for
Developing an Air Quality (Ozone and PM2.5)
Forecasting Program,’’ can be found at
https://www.airnow.gov/publications/
weathercasters/guidelines-developing-airquality-forecasting-program/.
3.4 Calculation and Equations.
i. The AQI is the highest value calculated
for each pollutant as follows:
a. Identify the highest concentration among
all of the monitors within each reporting area
and truncate as follows:
(1) Ozone—truncate to 3 decimal places
PM2.5—truncate to 1 decimal place
PM10—truncate to integer
CO—truncate to 1 decimal place
SO2—truncate to integer
NO2—truncate to integer
(2) [Reserved]
b. Using table 2 to this appendix, find the
two breakpoints that contain the
concentration.
c. Using equation 1 to this appendix,
calculate the index.
d. Round the index to the nearest integer.
TABLE 2 TO APPENDIX G TO PART 58—BREAKPOINTS FOR THE AQI
These breakpoints
O3
(ppm)
8-hour
O3
(ppm)
1-hour 1
PM2.5
(μg/m3)
24-hour
Equal these AQI’s
PM10
(μg/m3)
24-hour
CO
(ppm)
8-hour
SO2
(ppb)
1-hour
NO2
(ppb)
1-hour
AQI
Category
Good.
Moderate.
Unhealthy for Sensitive
Groups.
Unhealthy.
Very Unhealthy.
Hazardous.4
0.000–0.054
0.055–0.070
0.071–0.085
........................
........................
0.125–0.164
0.0–(9.0–10.0)
(9.1–10.1)–35.4
35.5–55.4
0–54
55–154
155–254
0.0–4.4
4.5–9.4
9.5–12.4
0–35
36–75
76–185
0–53
54–100
101–360
0–50
51–100
101–150
0.086–0.105
0.106–0.200
0.201–(2)
0.165–0.204
0.205–0.404
0.405+
55.5–125.4
125.5–225.4
225.5+
255–354
355–424
425+
12.5–15.4
15.5–30.4
30.5+
3 186–304
361–649
650–1249
1250+
151–200
201–300
301+
3 305–604
3 605+
1 Areas
ii. If the concentration is equal to a
breakpoint, then the index is equal to the
corresponding index value in table 2 to this
appendix. However, equation 1 to this
appendix can still be used. The results will
be equal. If the concentration is between two
breakpoints, then calculate the index of that
pollutant with equation 1. It should also be
noted that in some areas, the AQI based on
1-hour O3 will be more precautionary than
using 8-hour values (see footnote 1 to table
2). In these cases, the 1-hour values as well
as 8-hour values may be used to calculate
index values and then use the maximum
index value as the AQI for O3.
Where:
Ip = the index value for pollutantp.
Cp = the truncated concentration of
pollutantp.
BPHi = the breakpoint that is greater than or
equal to Cp.
BPLo = the breakpoint that is less than or
equal to Cp.
IHi = the AQI value corresponding to BPHi.
Ilo = the AQI value corresponding to BPLo.
iii. If the concentration is larger than the
highest breakpoint in table 2 to this appendix
then the last two breakpoints in table 2 may
be used when equation 1 to this appendix is
applied.
a. Find the breakpoints for PM10 at 210 mg/
m3 as 155 mg/m3 and 254 mg/m3,
corresponding to index values 101 and 150;
b. Find the breakpoints for 1-hour O3 at
0.156 ppm as 0.125 ppm and 0.164 ppm,
corresponding to index values 101 and 150;
c. Find the breakpoints for 8-hour O3 at
0.130 ppm as 0.116 ppm and 0.374 ppm,
corresponding to index values 201 and 300;
d. Apply equation 1 to this appendix for
210 mg/m3, PM10:
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Example
iv. Using table 2 and equation 1 to this
appendix, calculate the index value for each
of the pollutants measured and select the one
that produces the highest index value for the
AQI. For example, if a PM10 value of 210 mg/
m3 is observed, a 1-hour O3 value of 0.156
ppm, and an 8-hour O3 value of 0.130 ppm,
then do this:
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Equation 1 to Appendix G to Part 58
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are generally required to report the AQI based on 8-hour ozone values. However, there are a small number of areas where an AQI
based on 1-hour ozone values would be more precautionary. In these cases, in addition to calculating the 8-hour ozone index value, the 1-hour
ozone index value may be calculated, and the maximum of the two values reported.
2 8-hour O concentrations do not define higher AQI values (>301). AQI values >301 are calculated with 1-hour O concentrations.
3
3
3 1-hr SO concentrations do not define higher AQI values (≥200). AQI values of 200 or greater are calculated with 24-hour SO concentration.
2
2
4 AQI values between breakpoints are calculated using equation 1 to this appendix. For AQI values in the hazardous category, AQI values
greater than 500 should be calculated using equation 1 and the concentration specified for the AQI value of 500. The AQI value of 500 are as
follows: O3 1-hour—0.604 ppm; PM2.5 24-hour—325.4 μg/m3; PM10 24-hour—604 μg/m3; CO ppm—50.4 ppm; SO2 1-hour—1004 ppb; and NO2
1-hour—2049 ppb.
Federal Register / Vol. 88, No. 18 / Friday, January 27, 2023 / Proposed Rules
150 101
254 - 155 210 - l55)
c
5719
+ 101 = 128
e. Apply equation 1 to this appendix for
0.156 ppm, 1-hour O3:
150 -101
0.164 - 0.125 (O.l 56 - 0.125)
+ 101 = 140
f. Apply equation 1 to this appendix for
0.130 ppm, 8-hour O3:
300 - 201
0.374 - 0.116 (o. 130 - 0.116)
g. Find the maximum, 206. This is the AQI.
A minimal AQI report could read: ‘‘Today,
+ 201 = 206
the AQI for my city is 206, which is Very
Unhealthy, due to ozone.’’ It would then
reference the associated sensitive groups.
[FR Doc. 2023–00269 Filed 1–26–23; 8:45 am]
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BILLING CODE 6560–50–P
Agencies
[Federal Register Volume 88, Number 18 (Friday, January 27, 2023)]
[Proposed Rules]
[Pages 5558-5719]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2023-00269]
[[Page 5557]]
Vol. 88
Friday,
No. 18
January 27, 2023
Part III
Environmental Protection Agency
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40 CFR Parts 50, 53, and 58
Reconsideration of the National Ambient Air Quality Standards for
Particulate Matter; Proposed Rule
Federal Register / Vol. 88 , No. 18 / Friday, January 27, 2023 /
Proposed Rules
[[Page 5558]]
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ENVIRONMENTAL PROTECTION AGENCY
40 CFR Parts 50, 53, and 58
[EPA-HQ-OAR-2015-0072; FRL-8635-01-OAR]
RIN 2060-AV52
Reconsideration of the National Ambient Air Quality Standards for
Particulate Matter
AGENCY: Environmental Protection Agency (EPA).
ACTION: Proposed rule.
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SUMMARY: Based on the Environmental Protection Agency's (EPA's)
reconsideration of the air quality criteria and the national ambient
air quality standards (NAAQS) for particulate matter (PM), the EPA
proposes to revise the primary annual PM2.5 standard by
lowering the level. The Agency proposes to retain the current primary
24-hour PM2.5 standard and the primary 24-hour
PM10 standard. The Agency also proposes not to change the
secondary 24-hour PM2.5 standard, secondary annual
PM2.5 standard, and secondary 24-hour PM10
standard at this time. The EPA also proposes revisions to other key
aspects related to the PM NAAQS, including revisions to the Air Quality
Index (AQI) and monitoring requirements for the PM NAAQS.
DATES: Comments must be received on or before March 28, 2023.
Public Hearings: The EPA will hold a virtual public hearing on this
proposed rule. This hearing will be announced in a separate Federal
Register document that provides details, including specific dates,
times, and contact information for these hearings.
ADDRESSES: You may submit comments, identified by Docket ID No. EPA-HQ-
OAR-2015-0072, by any of the following means:
Federal eRulemaking Portal: https://www.regulations.gov/
(our preferred method). Follow the online instructions for submitting
comments.
Email: [email protected]. Include the Docket ID No.
EPA-HQ-OAR-2015-0072 in the subject line of the message.
Mail: U.S. Environmental Protection Agency, EPA Docket
Center, Air and Radiation Docket, Mail Code 28221T, 1200 Pennsylvania
Avenue NW, Washington, DC 20460.
Hand Delivery or Courier (by scheduled appointment only):
EPA Docket Center, WJC West Building, Room 3334, 1301 Constitution
Avenue NW, Washington, DC 20004. The Docket Center's hours of
operations are 8:30 a.m.-4:30 p.m., Monday-Friday (except Federal
Holidays).
Instructions: All submissions received must include the Docket ID
No. for this document. Comments received may be posted without change
to https://www.regulations.gov, including any personal information
provided. For detailed instructions on sending comments and additional
information on the rulemaking process, see the SUPPLEMENTARY
INFORMATION section of this document.
FOR FURTHER INFORMATION CONTACT: Dr. Lars Perlmutt, Health and
Environmental Impacts Division, Office of Air Quality Planning and
Standards, U.S. Environmental Protection Agency, Mail Code C539-04,
Research Triangle Park, NC 27711; telephone: (919) 541-3037; fax: (919)
541-5315; email: [email protected].
SUPPLEMENTARY INFORMATION:
General Information
Preparing Comments for the EPA
Follow the online instructions for submitting comments. Once
submitted to the Federal eRulemaking Portal, comments cannot be edited
or withdrawn. The EPA may publish any comment received to its public
docket. Do not submit electronically any information you consider to be
Confidential Business Information (CBI) or other information whose
disclosure is restricted by statute. Multimedia submissions (audio,
video, etc.) must be accompanied by a written submission. The written
comment is considered the official comment and should include
discussion of all points you wish to make. The EPA will generally not
consider comments or comment contents located outside of the primary
submission (i.e., on the web, the cloud, or other file sharing system).
For additional submission methods, the full EPA public comment policy,
information about CBI or multimedia submissions, and general guidance
on making effective comments, please visit https://www.epa.gov/dockets/commenting-epa-dockets.
When submitting comments, remember to:
Identify the action by docket number and other identifying
information (subject heading, Federal Register date and page number).
Explain why you agree or disagree, suggest alternatives,
and substitute language for your requested changes.
Describe any assumptions and provide any technical
information and/or data that you used.
Provide specific examples to illustrate your concerns and
suggest alternatives.
Explain your views as clearly as possible, avoiding the
use of profanity or personal threats.
Make sure to submit your comments by the comment period
deadline identified.
Availability of Information Related to This Action
All documents in the dockets pertaining to this action are listed
on the www.regulations.gov website. This includes documents in the
docket for the proposed decision (Docket ID No. EPA-HQ-OAR-2015-0072)
and a separate docket, established for the Integrated Science
Assessment (ISA) (Docket ID No. EPA-HQ-ORD-2014-0859) that has been
adopted by reference into the docket for this proposed decision.
Although listed in the index, some information is not publicly
available, e.g., CBI or other information whose disclosure is
restricted by statute. Certain other material, such as copyrighted
material, is not placed on the internet and may be viewed with prior
arrangement with the EPA Docket Center. Additionally, a number of the
documents that are relevant to this proposed decision are available
through the EPA's website at https://www.epa.gov/naaqs/particulate-matter-pm-air-quality-standards. These documents include the Integrated
Science Assessment for Particulate Matter (U.S. EPA, 2019a), available
at https://cfpub.epa.gov/ncea/isa/recordisplay.cfm?deid=347534, the
Supplement to the 2019 Integrated Science Assessment for Particulate
Matter (U.S. EPA, 2022a), available at https://cfpub.epa.gov/ncea/isa/recordisplay.cfm?deid=354490, and the Policy Assessment for the
Reconsideration of the National Ambient Air Quality Standards for
Particulate Matter (U.S. EPA, 2022b), available at https://www.epa.gov/naaqs/particulate-matter-pm-standards-integrated-science-assessments-current-review.
Table of Contents
The following topics are discussed in this preamble:
Executive Summary
I. Background
A. Legislative Requirements
B. Related PM Control Programs
C. Review of the Air Quality Criteria and Standards for
Particulate Matter
1. Reviews Completed in 1971 and 1987
2. Review Completed in 1997
3. Review Completed in 2006
4. Review Completed in 2012
[[Page 5559]]
5. Review Completed in 2020
6. Reconsideration of the 2020 PM NAAQS Final Action
a. Decision To Initiate a Reconsideration
b. Process for Reconsideration of the 2020 PM NAAQS Decision
D. Air Quality Information
1. Distribution of Particle Size in Ambient Air
2. Sources and Emissions Contributing to PM in the Ambient Air
3. Monitoring of Ambient PM
4. Ambient Concentrations and Trends
a. PM2.5 Mass
b. PM2.5 Components
c. PM10
d. PM10-2.5
e. UFP
5. Characterizing Ambient PM2.5 Concentrations for
Exposure
a. Predicted Ambient PM2.5 and Exposure Based on
Monitored Data
b. Comparison of PM2.5 Fields in Estimating Exposure
and Relative to Design Values
6. Background PM
II. Rationale for Proposed Decisions on the Primary PM2.5
Standards
A. General Approach
1. Background on the Current Standards
a. Considerations Regarding the Adequacy of the Existing
Standards in the 2020 Review
2. General Approach and Key Issues in This Reconsideration of
the 2020 Final Decision
B. Overview of the Health Effects Evidence
1. Nature of Effects
a. Mortality
b. Cardiovascular Effects
c. Respiratory Effects
d. Cancer
e. Nervous System Effects
f. Other Effects
2. Public Health Implications and At-Risk Populations
3. PM2.5 Concentrations in Key Studies Reporting
Health Effects
a. PM2.5 Exposure Concentrations Evaluated in
Experimental Studies
b. Ambient PM2.5 Concentrations in Locations of
Epidemiologic Studies
4. Uncertainties in the Health Effects Evidence
C. Summary of Exposure and Risk Estimates
1. Key Design Aspects
2. Key Limitations and Uncertainties
3. Summary of Risk Estimates
D. Proposed Conclusions on the Primary PM2.5
Standards
1. CASAC Advice in This Reconsideration
2. Evidence- and Risk-Based Considerations in the Policy
Assessment
a. Evidence-Based Considerations
b. Risk-Based Considerations
3. Administrator's Proposed Conclusions on the Primary
PM2.5 Standards
a. Adequacy of the Current Primary PM2.5 Standards
b. Consideration of Alternative Primary Annual PM2.5
Standard Levels
E. Proposed Decisions on the Primary PM2.5 Standards
III. Rationale for Proposed Decisions on the Primary PM10
Standard
A. General Approach
1. Background on the Current Standard
i. Considerations Regarding the Adequacy of the Existing
Standard in the 2020 Review
2. General Approach and Key Issues in This Reconsideration of
the 2020 Final Decision
B. Overview of Health Effects Evidence
1. Nature of Effects
a. Mortality
i. Long-Term Exposures
ii. Short-Term Exposures
b. Cardiovascular Effects
i. Long-Term Exposures
ii. Short-Term Exposures
c. Respiratory Effects--Short-Term Exposures
d. Cancer--Long-Term Exposures
e. Metabolic Effects--Long-Term Exposures
f. Nervous System Effects--Long-Term Exposures
C. Proposed Conclusions on the Primary PM10 Standard
1. CASAC Advice in This Reconsideration
2. Evidence-Based Considerations in the Policy Assessment
3. Administrator's Proposed Decision on the Current Primary
PM10 Standard
IV. Communication of Public Health
A. Air Quality Index Overview
B. Air Quality Index Category Breakpoints for PM2.5
1. Air Quality Index Values of 50, 100 and 150
2. Air Quality Index Values of 200 and 300
3. Air Quality Index Value of 500
C. Air Quality Index Category Breakpoints for PM10
D. Air Quality Index Reporting
V. Rationale for Proposed Decisions on the Secondary PM Standards
A. General Approach
1. Background on the Current Standards
a. Non-Visibility Effects
i. Considerations Regarding Adequacy of the Existing Standards
for Non-Visibility Effects in the 2020 Review
b. Visibility Effects
i. Considerations Regarding Adequacy of the Existing Standards
for Visibility Effects in the 2020 Review
2. General Approach and Key Issues in This Reconsideration of
the 2020 Final Decision
B. Overview of Welfare Effects Evidence
1. Nature of Effects
a. Visibility
b. Climate
c. Materials
C. Summary of Air Quality and Quantitative Information
1. Visibility Effects
a. Target Level of Protection in Terms of a PM2.5
Visibility Index
b. Relationship Between the PM2.5 Visibility Index
and the Current Secondary 24-Hour PM2.5 Standard
2. Non-Visibility Effects
D. Proposed Conclusions on the Secondary PM Standards
1. CASAC Advice in This Reconsideration
2. Evidence- and Quantitative Information-Based Considerations
in the Policy Assessment
3. Administrator's Proposed Decision on the Current Secondary PM
Standards
VI. Interpretation of the NAAQS for PM
A. Proposed Amendments to Appendix K: Interpretation of the
NAAQS for Particulate Matter
1. Updating Design Value Calculations To Be on a Site-Level
Basis
2. Codifying Site Combinations To Maintain a Continuous Data
Record
3. Clarifying Daily Validity Requirements for Continuous
Monitors
B. Proposed Amendments to Appendix N: Interpretation of the
NAAQS for PM2.5
1. Updating References to the Proposed Revision(s) of the
Standards
2. Codifying Site Combinations To Maintain a Continuous Data
Record
VII. Proposed Amendments to Ambient Monitoring and Quality Assurance
Requirements
A. Proposed Amendment in 40 CFR Part 50 (Appendix L): Reference
Method for the Determination of Fine Particulate Matter as
PM2.5 in the Atmosphere--Addition of the Tisch Cyclone as
an Approved Second Stage Separator
B. Issues Related to 40 CFR Part 53 (Reference and Equivalent
Methods)
1. Update to Program Title and Delivery Address for FRM and FEM
Application and Modification Requests
2. Requests for Delivery of a Candidate FRM or FEM Instrument
3. Amendments to Requirements for Submission of Materials in
Sec. 53.4(b)(7) for Language and Format
4. Amendment to Designation of Reference and Equivalent Methods
5. Amendment to One Test Field Campaign Requirement for Class
III PM2.5 FEMs
6. Amendment to Use of Monodisperse Aerosol Generator
7. Corrections to 40 CFR Part 53 (Reference and Equivalent
Methods)
C. Proposed Changes to 40 CFR Part 58 (Ambient Air Quality
Surveillance)
1. Quality Assurance Requirements for Monitors Used in
Evaluations for National Ambient Air Quality Standards
a. Quality System Requirements
b. Measurement Quality Check Requirements
c. Calculations for Data Quality Assessments
d. References
2. Quality Assurance Requirements for Prevention of Significant
Deterioration (PSD) Air Monitoring
a. Quality System Requirements
b. Measurement Quality Check Requirements
c. Calculations for Data Quality Assessments
d. References
3. Proposed Amendments to PM Ambient Air Quality Methodology
a. Proposal To Revoke Approved Regional Methods (ARMs)
b. Proposal for Calibration of PM Federal Equivalent Methods
(FEMs)
4. Proposed Amendment to the PM2.5 Monitoring Network
Design Criteria To Address At-Risk Communities
5. Proposed Revisions To Probe and Monitoring Path Siting
Criteria
a. Providing Separate Section for Open Path Monitoring
Requirements
[[Page 5560]]
b. Amending Distance Precision for Spacing Offsets
c. Clarifying Summary Table of Probe Siting Criteria
d. Adding Flexibility for the Spacing From Minor Sources
e. Amendments and Clarification for the Spacing From
Obstructions and Trees
f. Reinstating Minimum 270-Degree Arc and Clarifying 180-Degree
Arc in Regulatory Text
g. Clarification on Obstacles That Act as an Obstruction
h. Amending and Clarifying the 10-Meter Tree Dripline
Requirement
i. Amending Spacing Requirement for Microscale Monitoring
j. Amending Waiver Provisions
k. Broadening of Acceptable Probe Materials
D. Taking Comment on Incorporating Data From Next Generation
Technologies
1. Background on Use of FRM and FEM Monitors
2. Next Generation Technologies: Data Considerations
3. PM2.5 Continuous FEMs
4. PM2.5 Satellite Products
5. Use of Air Sensors
6. Summary
VIII. Clean Air Act Implementation Requirements for the PM NAAQS
A. Designation of Areas
B. Section 110(a)(1) and (2) Infrastructure SIP Requirements
C. Implementing Any Revised PM2.5 NAAQS in
Nonattainment Areas
D. Implementing the Primary and Secondary PM10 NAAQS
E. Prevention of Significant Deterioration and Nonattainment New
Source Review Programs for the Proposed Revised Primary Annual
PM2.5 NAAQS
F. Transportation Conformity Program
G. General Conformity Program
IX. Statutory and Executive Order Reviews
A. Executive Order 12866: Regulatory Planning and Review and
Executive Order 13563: Improving Regulation and Regulatory Review
B. Paperwork Reduction Act (PRA)
C. Regulatory Flexibility Act (RFA)
D. Unfunded Mandates Reform Act (UMRA)
E. Executive Order 13132: Federalism
F. Executive Order 13175: Consultation and Coordination With
Indian Tribal Governments
G. Executive Order 13045: Protection of Children From
Environmental Health and Safety Risks
H. Executive Order 13211: Actions Concerning Regulations That
Significantly Affect Energy Supply, Distribution or Use
I. National Technology Transfer and Advancement Act (NTTAA)
J. Executive Order 12898: Federal Actions To Address
Environmental Justice in Minority Populations and Low-Income
Populations
References
Executive Summary
This document presents the Administrator's proposed decisions for
the reconsideration of the 2020 final decision on the primary (health-
based) and secondary (welfare-based) National Ambient Air Quality
Standards (NAAQS) for Particulate Matter (PM). More specifically this
document summarizes the background and rationale for the
Administrator's proposed decisions to revise the primary annual
PM2.5 standard by lowering the level from 12.0 [micro]g/m\3\
to within the range of 9.0 to 10.0 [micro]g/m\3\ while taking comment
on alternative annual standard levels down to 8.0 [micro]g/m\3\ and up
to 11.0 [micro]g/m\3\; to retain the current primary 24-hour
PM2.5 standard (at a level of 35 [micro]g/m\3\) while taking
comment on revising the level as low as 25 [micro]g/m\3\; to retain the
primary 24-hour PM10 standard, without revision; and, not to
change the secondary PM standards at this time, while taking comment on
revising the level of the secondary 24-hour PM2.5 standard
as low as 25 [micro]g/m\3\. In reaching his proposed decisions, the
Administrator has considered the currently available scientific
evidence in the 2019 Integrated Science Assessment (2019 ISA) and the
Supplement to the 2019 ISA (ISA Supplement), quantitative and policy
analyses presented in the Policy Assessment (PA), and advice from the
Clean Air Scientific Advisory Committee (CASAC). The EPA solicits
comment on the proposed decisions described here and on the array of
issues associated with the reconsideration of these standards,
including the judgments of public health, public welfare and science
policy inherent in the proposed decisions, and requests commenters also
provide the rationales upon which views articulated in submitted
comments are based.
The EPA has established primary and secondary standards for
PM2.5, which includes particles with diameters generally
less than or equal to 2.5 [micro]m, and PM10, which includes
particles with diameters generally less than or equal to 10 [micro]m.
The standards include two primary PM2.5 standards, an annual
average standard, averaged over three years, with a level of 12.0
[micro]g/m\3\ and a 24-hour standard with a 98th percentile form,
averaged over three years, and a level of 35 [micro]g/m\3\. It also
includes a primary PM10 standard with a 24-hour averaging
time, and a level of 150 [micro]g/m\3\, not to be exceeded more than
once per year on average over three years. Secondary PM standards are
set equal to the primary standards, except that the level of the
secondary annual PM2.5 standard is 15.0 [micro]g/m\3\.
The last review of the PM NAAQS was completed in December 2020. In
that review, the EPA retained the primary and secondary NAAQS, without
revision (85 FR 82684, December 18, 2020). Following publication of the
2020 final action, several parties filed petitions for review and
petitions for reconsideration of the EPA's final decision.
In June 2021, the Agency announced its decision to reconsider the
2020 PM NAAQS final action.\1\ The EPA is reconsidering the December
2020 decision because the available scientific evidence and technical
information indicate that the current standards may not be adequate to
protect public health and welfare, as required by the Clean Air Act.
The EPA noted that the 2020 PA concluded that the scientific evidence
and information called into question the adequacy of the primary
PM2.5 standards and supported consideration of revising the
level of the primary annual PM2.5 standard to below the
current level of 12.0 [micro]g/m\3\ while retaining the primary 24-hour
PM2.5 standard (U.S. EPA, 2020a). The EPA also noted that
the 2020 PA concluded that the available scientific evidence and
information did not call into question the adequacy of the primary
PM10 or secondary PM standards and supported consideration
of retaining the primary PM10 standard and secondary PM
standards without revision (U.S. EPA, 2020a).
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\1\ The press release for this announcement is available at:
https://www.epa.gov/newsreleases/epa-reexamine-health-standards-harmful-soot-previous-administration-left-unchanged.
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The proposed decisions presented in this document on the primary
PM2.5 standards have been informed by key aspects of the
available health effects evidence and conclusions contained in the 2019
ISA and ISA Supplement, quantitative exposure/risk analyses and policy
evaluations presented in the PA, advice from the CASAC \2\ and public
comment received as part of this reconsideration.\3\ The health effects
evidence available in this reconsideration, in conjunction with the
full body of evidence critically evaluated in the 2019 ISA, supports a
causal relationship between long- and
[[Page 5561]]
short-term exposures and mortality and cardiovascular effects, and the
evidence supports a likely to be a causal relationship between long-
term exposures and respiratory effects, nervous system effects, and
cancer. The longstanding evidence base, including animal toxicological
studies, controlled human exposure studies, and epidemiologic studies,
reaffirms, and in some cases strengthens, the conclusions from past
reviews regarding the health effects of PM2.5 exposures.
Epidemiologic studies available in this reconsideration demonstrate
generally positive, and often statistically significant,
PM2.5 health effect associations. Such studies report
associations between estimated PM2.5 exposures and non-
accidental, cardiovascular, or respiratory mortality; cardiovascular or
respiratory hospitalizations or emergency room visits; and other
mortality/morbidity outcomes (e.g., lung cancer mortality or incidence,
asthma development). The scientific evidence available in this
reconsideration, as evaluated in the 2019 ISA and ISA Supplement,
includes a number of epidemiologic studies that use various methods to
characterize exposure to PM2.5 (e.g., ground-based monitors
and hybrid modeling approaches) and to evaluate associations between
health effects and lower ambient PM2.5 concentrations. There
are a number of recent epidemiologic studies that use varying study
designs that reduce uncertainties related to confounding and exposure
measurement error. The results of these analyses provide further
support for the robustness of associations between PM2.5
exposures and mortality and morbidity. Moreover, the Administrator
notes that recent epidemiologic studies strengthen support for health
effect associations at lower PM2.5 concentrations, with
these new studies finding positive and significant associations when
assessing exposure in locations and time periods with lower mean and
25th percentile concentrations than those evaluated in epidemiologic
studies available at the time of previous reviews. Additionally, the
experimental evidence (i.e., animal toxicological and controlled human
exposure studies) strengthens the coherence of effects across
scientific disciplines and provides additional support for potential
biological pathways through which PM2.5 exposures could lead
to the overt population-level outcomes reported in epidemiologic
studies for the health effect categories for which a causal
relationship (i.e., short- and long-term PM2.5 exposure and
mortality and cardiovascular effects) or likely to be causal
relationship (i.e., short- and long-term PM2.5 exposure and
respiratory effects; and long-term PM2.5 exposure and
nervous system effects and cancer) was concluded.
---------------------------------------------------------------------------
\2\ In 2021, the Administrator announced his decision to
reestablish the membership of the CASAC. The Administrator selected
seven members to serve on the chartered CASAC, and appointed a PM
CASAC panel to support the chartered CASAC's review of the draft ISA
Supplement and the draft PA as a part of this reconsideration (see
section I.C.6.b below for more information).
\3\ More information regarding the CASAC review of the draft ISA
Supplement and the draft PA, including opportunities for public
comment, can be found in the following Federal Register notices: 86
FR 54186, September 30, 2021; 86 FR 52673, September 22, 2021; 86 FR
56263, October 8, 2021; 87 FR 958, January 7, 2022.
---------------------------------------------------------------------------
The available evidence in the 2019 ISA continues to provide support
for factors that may contribute to increased risk of PM2.5-
related health effects including lifestage (children and older adults),
pre-existing diseases (cardiovascular disease and respiratory disease),
race/ethnicity, and socioeconomic status. For example, the 2019 ISA and
ISA Supplement conclude that there is strong evidence that Black and
Hispanic populations, on average, experience higher PM2.5
exposures and PM2.5-related health risk than non-Hispanic
White populations. In addition, studies evaluated in the 2019 ISA and
ISA Supplement also provide evidence indicating that communities with
lower socioeconomic status (SES), as assessed in epidemiologic studies
using indicators of SES including income and educational attainment
are, on average, exposed to higher concentrations of PM2.5
compared to higher SES communities.
The quantitative risk assessment, as well as policy considerations
in the PA, also inform the proposed decisions on the primary
PM2.5 standards. The risk assessment in this consideration
focuses on all-cause or nonaccidental mortality associated with long-
and short-term PM2.5 exposures. The primary analyses focus
on exposure and risk associated with air quality that might occur in an
area under air quality conditions that just meet the current and
potential alternative standards. The risk assessment estimates that the
current primary PM2.5 standards could allow a substantial
number of PM2.5-associated premature deaths in the United
States, and that public health improvements would be associated with
just meeting all of the alternative (more stringent) annual and 24-hour
standard levels modeled. Additionally, the results of the risk
assessment suggest that for most of the U.S., the annual standard is
the controlling standard and that revision to that standard has the
most potential to reduce PM2.5 exposure related risk.
Further analyses comparing the reductions in average national
PM2.5 concentrations and risk rates within each demographic
population estimate that the average percent PM2.5
concentrations and risk reductions are slightly greater in the Black
population than in the White population when meeting a revised annual
standard with a lower level. The analyses are summarized in this
document and described in detail in the PA.
In its advice to the Administrator, the CASAC concurred with the
draft PA that the currently available health effects evidence calls
into question the adequacy of the primary annual PM2.5
standard. With regard to the primary annual PM2.5 standard,
the majority of the CASAC concluded that the level of the standard
should be revised within the range of 8.0 to 10.0 [micro]g/m\3\, while
the minority of the CASAC concluded that the primary annual
PM2.5 standard should be revised to a level of 10.0 to 11.0
[micro]g/m\3\. With regard to the primary 24-hour PM2.5
standard, the majority of the CASAC concluded that the primary 24-hour
PM2.5 was not adequate and that the level of the standard
should be revised to within the range of 25 to 30 [micro]g/m\3\, while
the minority of the CASAC concluded that the primary 24-hour
PM2.5 standard was adequate and should be retained, without
revision.
In considering how to revise the suite of standards to provide the
requisite degree of protection, the Administrator recognizes that the
current annual standard and 24-hour standard, together, are intended to
provide public health protection against the full distribution of
short- and long-term PM2.5 exposures. Further, he recognizes
that changes in PM2.5 air quality designed to meet either
the annual or the 24-hour standard would likely result in changes to
both long-term average and short-term peak PM2.5
concentrations. Based on the current evidence and quantitative
information, as well as consideration of CASAC advice and public
comment thus far in this reconsideration, the Administrator proposes to
conclude that the current primary PM2.5 standards are not
adequate to protect public health with an adequate margin of safety.
The Administrator also notes that the CASAC was unanimous in its
advice regarding the need to revise the annual standard. In considering
the appropriate level for a revised annual standard, the Administrator
provisionally concludes that a standard set within the range of 9.0 to
10.0 [micro]g/m\3\ would reflect his placing the most weight on the
strongest available evidence while appropriately weighing the
uncertainties. In addition, the Administrator recognizes that some
members of CASAC advised, and the PA concluded, that the available
scientific information provides support for considering a range that
extends up to 11.0 [micro]g/m\3\ and down to 8.0 [micro]g/m\3\.
With regard to the primary 24-hour PM2.5 standard, the
Administrator finds it is less clear whether the available scientific
evidence and quantitative
[[Page 5562]]
information calls into question the adequacy of the public health
protection afforded by the current 24-hour standard. He notes that a
more stringent annual standard is expected to reduce both average
(annual) concentrations and peak (daily) concentrations. Furthermore,
he notes that the CASAC did not reach consensus on whether revisions to
the primary 24-hour PM2.5 standard were warranted at this
time. The majority of the CASAC recommended that the level of the
current primary 24-hour PM2.5 should be revised to within
the range of 25 to 30 [micro]g/m\3\, while the minority of the CASAC
recommended retaining the current standard. The Administrator proposes
to conclude that the 24-hour standard should be retained, particularly
when considered in conjunction with the protection provided by the
suite of standards and the proposed decision to revise the annual
standard to a level of 9.0 to 10.0 [micro]g/m\3\.
The EPA solicits comment on the Administrator's proposed
conclusions, and on the proposed decision to revise the primary annual
PM2.5 standard and retain the primary 24-hour
PM2.5 standard, without revision. The Administrator is
conscious of his obligation to set primary standards with an adequate
margin of safety and preliminarily determines that the proposed
decision balances the need to provide protection against uncertain
risks with the obligation to not set standards that are more stringent
than necessary. The requirement to provide an adequate margin of safety
was intended to address uncertainties associated with inconclusive
scientific and technical information and to provide a reasonable degree
of protection against hazards that research has not yet identified.
Reaching decisions on what standards are appropriate necessarily
requires judgments of the Administrator about how to consider the
information available from the epidemiologic studies and other relevant
evidence. In the Administrator's judgment, the proposed suite of
primary PM2.5 standards reflects the appropriate
consideration of the strength of the available evidence and other
information and their associated uncertainties and the advice of the
CASAC. The final rulemaking will reflect the Administrator's ultimate
judgments as to the suite of primary PM2.5 standards that
are requisite to protect the public health with an adequate margin of
safety. Consistent with these principles, the EPA also solicits public
comment on alternative annual standard levels down to 8.0 [micro]g/m\3\
and up to 11.0 [micro]g/m\3\, on an alternative 24-hour standard level
as low as 25 [micro]g/m\3\ and on the combination of annual and 24-hour
standards that commenters may believe is appropriate, along with the
approaches and scientific rationales used to support such levels. For
example, the EPA solicits comments on the uncertainties in the reported
associations between daily or annual average PM2.5 exposures
and mortality or morbidity in the epidemiologic studies, the
significance of the 25th percentile of ambient concentrations reported
in studies, the relevance and limitations of international studies, and
other topics discussed in section II.D.3.b.
The primary PM10 standard is intended to provide public
health protection against health effects related to exposures to
PM10-2.5, which are particles with a diameter between 10
[micro]m and 2.5 [micro]m. The proposed decision to retain the current
24-hour PM10 standard has been informed by key aspects of
the available health effects evidence and conclusions contained in the
2019 ISA, the policy evaluations presented in the PA, advice from the
CASAC and public comment received as part of this reconsideration.
Specifically, the health effects evidence for PM10-2.5
exposures is somewhat strengthened since past reviews, although the
strongest evidence still only provides support for a suggestive of, but
not sufficient to infer, causal relationship with long- and short-term
exposures and mortality and cardiovascular effects, short-term
exposures and respiratory effects, and long-term exposures and cancer,
nervous system effects, and metabolic effects. In reaching his proposed
decision, the Administrator recognizes that, while the available health
effects evidence has expanded, recent studies are subjected to the same
types of uncertainties that were judged to be important in previous
reviews. He also recognizes that the CASAC generally agreed with the
draft PA that it was reasonable to retain the primary 24-hour
PM10 standard given the available scientific evidence,
including PM10 as an appropriate indicator. He proposes to
conclude that the newly available evidence does not call into question
the adequacy of the current primary PM10 standard, and he
proposes to retain that standard, without revision.
This reconsideration of the secondary PM standards focuses on
visibility, climate, and materials effects.\4\ The Administrator's
proposed decision to not change the current secondary standards at this
time has been informed by key aspects of the currently available
welfare effects evidence as well as the conclusions contained in the
2019 ISA and ISA Supplement; quantitative analyses of visibility
impairment; policy evaluations presented in the PA; advice from the
CASAC; and public comment received as part of this reconsideration.
Specifically, the welfare effects evidence available in this
reconsideration is consistent with the evidence available in previous
reviews and supports a causal relationship between PM and visibility,
climate, and materials effects. With regard to climate and materials
effects, while the evidence has expanded since previous reviews,
uncertainties remain in the evidence and there are still significant
limitations in quantifying potential adverse effects from PM on climate
and materials for purposes of setting a standard. With regard to
visibility effects, the results of quantitative analyses of visibility
impairment are similar to those in previous reviews, and suggest that
in areas that meet the current secondary 24-hour PM2.5
standard that estimated light extinction in terms of a 3-year
visibility metric would be at or well below the upper end of the range
for the target level of protection (i.e., 30 deciviews (dv)). The CASAC
generally agreed with the draft PA that substantial uncertainties
remain in the scientific evidence for climate and materials effects. In
considering the available scientific evidence for climate and materials
effects, along with CASAC advice, the Administrator proposes to
conclude that it is appropriate to retain the existing secondary
standards and that it is not appropriate to establish any distinct
secondary PM standards to address non-visibility PM-related welfare
effects. With regard to visibility effects, while the Administrator
notes that the CASAC did not recommend revising either the target level
of protection for the visibility index or the level of the current
secondary 24-hour PM2.5 standard, the Administrator
[[Page 5563]]
recognizes that, should an alternative level be considered for the
visibility index, that the CASAC recommends also considering revisions
to the secondary 24-hour PM2.5 standard. In considering the
available evidence and quantitative information, with its inherent
uncertainties and limitations, the Administrator proposes not to change
the secondary PM standards at this time, and solicits comment on this
proposed decision. In addition, the Administrator additionally solicits
comment on the appropriateness of a target level of protection for
visibility below 30 dv and down as low as 25 dv, and of revising the
level of the current secondary 24-hour PM2.5 standard to a
level as low as 25 [micro]g/m\3\.
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\4\ Consistent with the 2016 Integrated Review Plan (U.S. EPA,
2016), other welfare effects of PM, such as ecological effects, are
being considered in the separate, on-going review of the secondary
NAAQS for oxides of nitrogen, oxides of sulfur and PM. Accordingly,
the public welfare protection provided by the secondary PM standards
against ecological effects such as those related to deposition of
nitrogen- and sulfur-containing compounds in vulnerable ecosystems
is being considered in that separate review. Thus, the
Administrator's conclusion in this reconsideration of the 2020 final
decision will be focused only and specifically on the adequacy of
public welfare protection provided by the secondary PM standards
from effects related to visibility, climate, and materials and
hereafter ``welfare effects'' refers to those welfare effects.
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Any proposed revisions to the PM NAAQS, if finalized, would trigger
a process under which states (and tribes, if they choose) make
recommendations to the Administrator regarding designations,
identifying areas of the country that either meet or do not meet the
new or revised PM NAAQS. Those areas that do not meet the PM NAAQS will
need to develop plans that demonstrate how they will meet the
standards. As part of these plans, states have the opportunity to use
tools to advance environmental justice, in this case for overburdened
communities in areas with high PM concentrations above the NAAQS, as
provided in current PM NAAQS implementation guidance to meet
requirements (80 FR 58010, 58136, August 25, 2016). The EPA is not
proposing changes to any of the current PM NAAQS implementation
programs in this proposed rulemaking, and therefore is not requesting
comment on any specific proposals related to implementation or
designations.
On other topics, the EPA proposes to make two sets of changes to
the PM2.5 sub-index of the AQI. First, the EPA proposes to
continue to use the approach used in the revisions to the AQI in 2012
(77 FR 38890, June 29, 2012) of setting the lower breakpoints (50, 100
and 150) to be consistent with the levels of the primary
PM2.5 annual and 24-hour standards and proposes to revise
the lower breakpoints to be consistent with any changes to the primary
PM2.5 standards that are part of this reconsideration. In so
doing, the EPA proposes to revise the AQI value of 50 within the range
of 9.0 and 10.0 [micro]g/m\3\ and proposes to retain the AQI values of
100 and 150 at 35.4 [micro]g/m\3\ and 55.4 [micro]g/m\3\, respectively.
Second, the EPA proposes to revise the upper AQI breakpoints (200 and
above) and to replace the linear-relationship approach used in 1999 (64
FR 42530, August 4, 1999) to set these breakpoints, with an approach
that more fully considers the PM2.5 health effects evidence
from controlled human exposure and epidemiologic studies that has
become available in the last 20 years. The EPA also proposes to revise
the AQI values of 200, 300 and 500 to 125.4 [micro]g/m\3\, 225.4
[micro]g/m\3\, and 325.4 [micro]g/m\3\, respectively. The EPA proposes
to finalize these changes to the PM2.5 AQI in conjunction
with the Agency's final decisions on the primary annual and 24-hour
PM2.5 standards, if proposed revisions to such standards are
promulgated. The EPA is soliciting comment on the proposed revisions to
the AQI. In addition, the EPA also proposes to revise the daily
reporting requirement from 5 days per week to 7 days per week, while
also reformatting appendix G and providing clarifications.
With regard to monitoring-related activities, the EPA proposes
revisions to data calculations and ambient air monitoring requirements
for PM to improve the usefulness of and appropriateness of data used in
regulatory decision making and to better characterize air quality in
communities that are at increased risk of PM2.5 exposure and
health risk. These proposed changes are found in 40 CFR part 50
(appendices K, L, and N), part 53, and part 58 with associated
appendices (A, B, C, D, and E). These proposed changes include
addressing updates in data calculations, approval of reference and
equivalent methods, updates in quality assurance statistical
calculations to account for lower concentration measurements, updates
to support improvements in PM methods, a revision to the
PM2.5 network design to account for at-risk populations, and
updates to the Probe and Monitoring Path Siting Criteria for NAAQS
pollutants.
In setting the NAAQS, the EPA may not consider the costs of
implementing the standards. This was confirmed by the Supreme Court in
Whitman v. American Trucking Associations, 531 U.S. 457, 465-472, 475-
76 (2001), as discussed in section II.A of this document. As has
traditionally been done in NAAQS rulemaking, the EPA prepared a
Regulatory Impact Analysis (RIA) to provide the public with information
on the potential costs and benefits of attaining several alternative
PM2.5 standard levels. In NAAQS rulemaking, the RIA is done
for informational purposes only, and the proposed decisions on the
NAAQS in this rulemaking are not based on consideration of the
information or analyses in the RIA. The RIA fulfills the requirements
of Executive Orders 13563 and 12866. The RIA estimates the costs and
monetized human health benefits of attaining three alternative annual
PM2.5 standard levels and one alternative 24-hour
PM2.5 standard level. Specifically, the RIA examines the
proposed annual and 24-hour alternative standard levels of 10/35
[micro]g/m\3\ and 9/35 [micro]g/m\3\, as well as the following two more
stringent alternative standard levels: (1) An alternative annual
standard level of 8 [micro]g/m\3\ in combination with the current 24-
hour standard (i.e., 8/35 [micro]g/m\3\), and (2) an alternative 24-
hour standard level of 30 [micro]g/m\3\ in combination with the
proposed annual standard level of 10 [micro]g/m\3\ (i.e., 10/30
[micro]g/m\3\). The RIA presents estimates of the costs and benefits of
applying illustrative national control strategies in 2032 after
implementing existing and expected regulations and assessing emissions
reductions to meet the current annual and 24-hour particulate matter
NAAQS (12/35 [micro]g/m\3\).
I. Background
A. Legislative Requirements
Two sections of the Clean Air Act (CAA) govern the establishment
and revision of the NAAQS. Section 108 (42 U.S.C. 7408) directs the
Administrator to identify and list certain air pollutants and then to
issue air quality criteria for those pollutants. The Administrator is
to list those pollutants ``emissions of which, in his judgment, cause
or contribute to air pollution which may reasonably be anticipated to
endanger public health or welfare''; ``the presence of which in the
ambient air results from numerous or diverse mobile or stationary
sources''; and for which he ``plans to issue air quality criteria. . .
.'' (42 U.S.C. 7408(a)(1)). Air quality criteria are intended to
``accurately reflect the latest scientific knowledge useful in
indicating the kind and extent of all identifiable effects on public
health or welfare which may be expected from the presence of [a]
pollutant in the ambient air. . . .'' (42 U.S.C. 7408(a)(2)).
Section 109 [42 U.S.C. 7409] directs the Administrator to propose
and promulgate ``primary'' and ``secondary'' NAAQS for pollutants for
which air quality criteria are issued [42 U.S.C. 7409(a)]. Section
109(b)(1) defines primary standards as ones ``the attainment and
maintenance of which in the judgment of the Administrator, based on
such criteria and allowing an adequate margin of safety, are requisite
to protect the public health.'' \5\ Under
[[Page 5564]]
section 109(b)(2), a secondary standard must ``specify a level of air
quality the attainment and maintenance of which, in the judgment of the
Administrator, based on such criteria, is requisite to protect the
public welfare from any known or anticipated adverse effects associated
with the presence of [the] pollutant in the ambient air.'' \6\
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\5\ The legislative history of section 109 indicates that a
primary standard is to be set at ``the maximum permissible ambient
air level . . . which will protect the health of any [sensitive]
group of the population,'' and that for this purpose ``reference
should be made to a representative sample of persons comprising the
sensitive group rather than to a single person in such a group.'' S.
Rep. No. 91-1196, 91st Cong., 2d Sess. 10 (1970).
\6\ Under CAA section 302(h) (42 U.S.C. 7602(h)), effects on
welfare include, but are not limited to, ``effects on soils, water,
crops, vegetation, manmade materials, animals, wildlife, weather,
visibility, and climate, damage to and deterioration of property,
and hazards to transportation, as well as effects on economic values
and on personal comfort and well-being.''
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In setting primary and secondary standards that are ``requisite''
to protect public health and welfare, respectively, as provided in
section 109(b), the EPA's task is to establish standards that are
neither more nor less stringent than necessary. In so doing, the EPA
may not consider the costs of implementing the standards. See generally
Whitman v. American Trucking Associations, 531 U.S. 457, 465-472, 475-
76 (2001). Likewise, ``[a]ttainability and technological feasibility
are not relevant considerations in the promulgation of national ambient
air quality standards.'' American Petroleum Institute v. Costle, 665
F.2d 1176, 1185 (D.C. Cir. 1981); accord Murray Energy Corporation v.
EPA, 936 F.3d 597, 623-24 (D.C. Cir. 2019).
The requirement that primary standards provide an adequate margin
of safety was intended to address uncertainties associated with
inconclusive scientific and technical information available at the time
of standard setting. It was also intended to provide a reasonable
degree of protection against hazards that research has not yet
identified. See Lead Industries Association v. EPA, 647 F.2d 1130, 1154
(D.C. Cir 1980); American Petroleum Institute v. Costle, 665 F.2d at
1186; Coalition of Battery Recyclers Ass'n v. EPA, 604 F.3d 613, 617-18
(D.C. Cir. 2010); Mississippi v. EPA, 744 F.3d 1334, 1353 (D.C. Cir.
2013). Both kinds of uncertainties are components of the risk
associated with pollution at levels below those at which human health
effects can be said to occur with reasonable scientific certainty.
Thus, in selecting primary standards that include an adequate margin of
safety, the Administrator is seeking not only to prevent pollution
levels that have been demonstrated to be harmful but also to prevent
lower pollutant levels that may pose an unacceptable risk of harm, even
if the risk is not precisely identified as to nature or degree. The CAA
does not require the Administrator to establish a primary NAAQS at a
zero-risk level or at background concentration levels, see Lead
Industries Ass'n v. EPA, 647 F.2d at 1156 n.51, Mississippi v. EPA, 744
F.3d at 1351, but rather at a level that reduces risk sufficiently so
as to protect public health with an adequate margin of safety.
In addressing the requirement for an adequate margin of safety, the
EPA considers such factors as the nature and severity of the health
effects involved, the size of the sensitive population(s), and the kind
and degree of uncertainties. The selection of any particular approach
to providing an adequate margin of safety is a policy choice left
specifically to the Administrator's judgment. See Lead Industries Ass'n
v. EPA, 647 F.2d at 1161-62; Mississippi v. EPA, 744 F.3d at 1353.
Section 109(d)(1) of the Act requires the review every five years
of existing air quality criteria and, if appropriate, the revision of
those criteria to reflect advances in scientific knowledge on the
effects of the pollutant on public health and welfare. Under the same
provision, the EPA is also to review every five years and, if
appropriate, revise the NAAQS, based on the revised air quality
criteria.
Section 109(d)(2) addresses the appointment and advisory functions
of an independent scientific review committee. Section 109(d)(2)(A)
requires the Administrator to appoint this committee, which is to be
composed of ``seven members including at least one member of the
National Academy of Sciences, one physician, and one person
representing State air pollution control agencies.'' Section
109(d)(2)(B) provides that the independent scientific review committee
``shall complete a review of the criteria . . . and the national
primary and secondary ambient air quality standards . . . and shall
recommend to the Administrator any new . . . standards and revisions of
existing criteria and standards as may be appropriate. . . .'' Since
the early 1980s, this independent review function has been performed by
the Clean Air Scientific Advisory Committee (CASAC) of the EPA's
Science Advisory Board.
As previously noted, the Supreme Court has held that section 109(b)
``unambiguously bars cost considerations from the NAAQS-setting
process.'' Whitman v. Am. Trucking Associations, 531 U.S. 457, 471
(2001). Accordingly, while some of these issues regarding which
Congress has directed the CASAC to advise the Administrator are ones
that are relevant to the standard setting process, others are not.
Issues that are not relevant to standard setting may be relevant to
implementation of the NAAQS once they are established.\7\
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\7\ Some aspects of the CASAC's advice may not be relevant to
the EPA's process of setting primary and secondary standards that
are requisite to protect public health and welfare. Indeed, were the
EPA to consider costs of implementation when reviewing and revising
the standards ``it would be grounds for vacating the NAAQS.''
Whitman, 531 U.S. at 471 n.4. At the same time, the CAA directs the
CASAC to provide advice on ``any adverse public health, welfare,
social, economic, or energy effects which may result from various
strategies for attainment and maintenance'' of the NAAQS to the
Administrator under section 109(d)(2)(C)(iv). In Whitman, the Court
clarified that most of that advice would be relevant to
implementation but not standard setting, as it ``enable[s] the
Administrator to assist the States in carrying out their statutory
role as primary implementers of the NAAQS.'' Id. at 470 (emphasis in
original). However, the Court also noted that the CASAC's ``advice
concerning certain aspects of `adverse public health . . . effects'
from various attainment strategies is unquestionably pertinent'' to
the NAAQS rulemaking record and relevant to the standard setting
process. Id. at 470 n.2.
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B. Related PM Control Programs
States are primarily responsible for ensuring attainment and
maintenance of ambient air quality standards once the EPA has
established them. Under section 110 and Part D, Subparts 1, 4 and 6 of
the CAA, and related provisions and regulations, states are to submit,
for the EPA's approval, state implementation plans (SIPs) that provide
for the attainment and maintenance of such standards through control
programs directed to sources of the pollutants involved. The states, in
conjunction with the EPA, also administer the prevention of significant
deterioration of air quality program that covers these pollutants (see
42 U.S.C. 7470-7479). In addition, Federal programs provide for or
result in nationwide reductions in emissions of PM and its precursors
under Title II of the Act, 42 U.S.C. 7521-7574, which involves controls
for motor vehicles and nonroad engines and equipment; the new source
performance standards under section 111 of the Act, 42 U.S.C. 7411; and
the national emissions standards for hazardous pollutants under section
112 of the Act, 42 U.S.C. 7412.
C. Review of the Air Quality Criteria and Standards for Particulate
Matter
1. Reviews Completed in 1971 and 1987
The EPA first established NAAQS for PM in 1971 (36 FR 8186, April
30, 1971), based on the original Air Quality
[[Page 5565]]
Criteria Document (AQCD) (DHEW, 1969).\8\ The Federal reference method
(FRM) specified for determining attainment of the original standards
was the high-volume sampler, which collects PM up to a nominal size of
25 to 45 [micro]m (referred to as total suspended particulates or TSP).
The primary standards were set at 260 [micro]g/m\3\, 24-hour average,
not to be exceeded more than once per year, and 75 [micro]g/m\3\,
annual geometric mean. The secondary standards were set at 150
[micro]g/m\3\, 24-hour average, not to be exceeded more than once per
year, and 60 [micro]g/m\3\, annual geometric mean.
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\8\ Prior to the review initiated in 2007 (see below), the AQCD
provided the scientific foundation (i.e., the air quality criteria)
for the NAAQS. Beginning in that review, the Integrated Science
Assessment (ISA) has replaced the AQCD.
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In October 1979 (44 FR 56730, October 2, 1979), the EPA announced
the first periodic review of the air quality criteria and NAAQS for PM.
Revised primary and secondary standards were promulgated in 1987 (52 FR
24634, July 1, 1987). In the 1987 decision, the EPA changed the
indicator for particles from TSP to PM10, in order to focus
on the subset of inhalable particles small enough to penetrate to the
thoracic region of the respiratory tract (including the
tracheobronchial and alveolar regions), referred to as thoracic
particles.\9\ The level of the 24-hour standards (primary and
secondary) was set at 150 [micro]g/m\3\, and the form was one expected
exceedance per year, on average over three years. The level of the
annual standards (primary and secondary) was set at 50 [micro]g/m\3\,
and the form was annual arithmetic mean, averaged over three years.
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\9\ PM10 refers to particles with a nominal mean
aerodynamic diameter less than or equal to 10 [micro]m. More
specifically, 10 [micro]m is the aerodynamic diameter for which the
efficiency of particle collection is 50 percent.
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2. Review Completed in 1997
In April 1994, the EPA announced its plans for the second periodic
review of the air quality criteria and NAAQS for PM, and in 1997 the
EPA promulgated revisions to the NAAQS (62 FR 38652, July 18, 1997). In
the 1997 decision, the EPA determined that the fine and coarse
fractions of PM10 should be considered separately. This
determination was based on evidence that serious health effects were
associated with short- and long-term exposures to fine particles in
areas that met the existing PM10 standards. The EPA added
new standards, using PM2.5 as the indicator for fine
particles (with PM2.5 referring to particles with a nominal
mean aerodynamic diameter less than or equal to 2.5 [micro]m). The new
primary standards were as follows: (1) an annual standard with a level
of 15.0 [micro]g/m\3\, based on the 3-year average of annual arithmetic
mean PM2.5 concentrations from single or multiple community-
oriented monitors;\10\ and (2) a 24-hour standard with a level of 65
[micro]g/m\3\, based on the 3-year average of the 98th percentile of
24-hour PM2.5 concentrations at each monitor within an area.
Also, the EPA established a new reference method for the measurement of
PM2.5 in the ambient air and adopted rules for determining
attainment of the new standards. To continue to address the health
effects of the coarse fraction of PM10 (referred to as
thoracic coarse particles or PM10-2.5; generally including
particles with a nominal mean aerodynamic diameter greater than 2.5
[micro]m and less than or equal to 10 [micro]m), the EPA retained the
primary annual PM10 standard and revised the form of the
primary 24-hour PM10 standard to be based on the 99th
percentile of 24-hour PM10 concentrations at each monitor in
an area. The EPA revised the secondary standards by setting them equal
in all respects to the primary standards.
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\10\ The 1997 annual PM2.5 standard was compared with
measurements made at the community-oriented monitoring site
recording the highest concentration or, if specific constraints were
met, measurements from multiple community-oriented monitoring sites
could be averaged (i.e., ``spatial averaging''). In the last review
(completed in 2012) the EPA replaced the term ``community-oriented''
monitor with the term ``area-wide'' monitor. Area-wide monitors are
those sited at the neighborhood scale or larger, as well as those
monitors sited at micro- or middle-scales that are representative of
many such locations in the same core-based statistical area (CBSA)
(78 FR 3236, January 15, 2013).
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Following promulgation of the 1997 PM NAAQS, petitions for review
were filed by several parties, addressing a broad range of issues. In
May 1999, the U.S. Court of Appeals for the District of Columbia
Circuit (D.C. Circuit) upheld the EPA's decision to establish fine
particle standards, holding that ``the growing empirical evidence
demonstrating a relationship between fine particle pollution and
adverse health effects amply justifies establishment of new fine
particle standards.'' American Trucking Associations, Inc. v. EPA, 175
F. 3d 1027, 1055-56 (D.C. Cir. 1999). The D.C. Circuit also found
``ample support'' for the EPA's decision to regulate coarse particle
pollution, but vacated the 1997 PM10 standards, concluding
that the EPA had not provided a reasonable explanation justifying use
of PM10 as an indicator for coarse particles. American
Trucking Associations v. EPA, 175 F. 3d at 1054-55. Pursuant to the
D.C. Circuit's decision, the EPA removed the vacated 1997
PM10 standards, and the pre-existing 1987 PM10
standards remained in place (65 FR 80776, December 22, 2000). The D.C.
Circuit also upheld the EPA's determination not to establish more
stringent secondary standards for fine particles to address effects on
visibility. American Trucking Associations v. EPA, 175 F. 3d at 1027.
The D.C. Circuit also addressed more general issues related to the
NAAQS, including issues related to the consideration of costs in
setting NAAQS and the EPA's approach to establishing the levels of
NAAQS. Regarding the cost issue, the court reaffirmed prior rulings
holding that in setting NAAQS the EPA is ``not permitted to consider
the cost of implementing those standards.'' American Trucking
Associations v. EPA, 175 F. 3d at 1040-41. Regarding the levels of
NAAQS, the court held that the EPA's approach to establishing the level
of the standards in 1997 (i.e., both for PM and for the ozone NAAQS
promulgated on the same day) effected ``an unconstitutional delegation
of legislative authority.'' American Trucking Associations v. EPA, 175
F. 3d at 1034-40. Although the court stated that ``the factors EPA uses
in determining the degree of public health concern associated with
different levels of ozone and PM are reasonable,'' it remanded the rule
to the EPA, stating that when the EPA considers these factors for
potential non-threshold pollutants ``what EPA lacks is any determinate
criterion for drawing lines'' to determine where the standards should
be set.
The D.C. Circuit's holding on the cost and constitutional issues
were appealed to the United States Supreme Court. In February 2001, the
Supreme Cour