Prevention of Significant Deterioration (PSD) for Particulate Matter Less Than 2.5 Micrometers (PM2.5, 54112-54156 [E7-18346]
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Federal Register / Vol. 72, No. 183 / Friday, September 21, 2007 / Proposed Rules
40 CFR Parts 51 and 52
[EPA–HQ–OAR–2006–0605; FRL–8470–1]
RIN 2060–AO24
Prevention of Significant Deterioration
(PSD) for Particulate Matter Less Than
2.5 Micrometers (PM2.5)—Increments,
Significant Impact Levels (SILs) and
Significant Monitoring Concentration
(SMC)
Environmental Protection
Agency (EPA).
ACTION: Proposed rule.
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AGENCY:
SUMMARY: The Clean Air Act (Act)
authorizes EPA to establish regulations
to prevent significant deterioration of air
quality due to emissions of any
pollutant for which a national ambient
air quality standard (NAAQS) has been
promulgated. The NAAQS for
particulate matter using the PM2.5
indicator were promulgated in 1997.
The EPA is proposing to facilitate
implementation of a PM2.5 Prevention of
Significant Deterioration (PSD) program
in areas attaining the particulate matter
less than 2.5 micrometers (PM2.5)
NAAQS by developing PM2.5
increments, Significant Impact Levels
(SILs), and a Significant Monitoring
Concentration (SMC). In addition, EPA
is proposing to revoke the annual PM10
increments.
‘‘Increments’’ are maximum increases
in ambient PM2.5 concentrations (PM2.5
increments) allowed in an area above
the baseline concentration. The SILs
and SMCs are numerical values that
represent thresholds of insignificant,
i.e., de minimis, modeled source
impacts or monitored (ambient)
concentrations, respectively. The EPA is
proposing such values for PM2.5 that
will be used as screening tools by a
major source subject to PSD to
determine the subsequent level of
analysis and data gathering required for
a PSD permit application for emissions
of PM2.5.
DATES: Comments must be received on
or before November 20, 2007. Under the
Paperwork Reduction Act, comments on
the information collection provisions
must be received by the Office of
Management and Budget (OMB) on or
before October 22, 2007.
Public Hearing. If anyone contacts us
requesting to speak at a public hearing
by October 11, 2007, we will hold a
public hearing. Additional information
about the hearing would be published in
a subsequent Federal Register notice.
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Submit your comments,
identified by Docket ID No. EPA–HQ–
OAR–2006–0605, by one of the
following methods:
• www.regulations.gov. Follow the
on-line instructions for submitting
comments.
• E-mail: a-and-r-Docket@.epa.gov.
• Mail: Air and Radiation Docket and
Information Center, Environmental
Protection Agency, Mailcode: 2822T,
1200 Pennsylvania Avenue, NW.,
Washington, DC 20460. Please include a
total of two copies. In addition, please
mail a copy of your comments on the
information collection provisions to the
Office of Information and Regulatory
Affairs, Office of Management and
Budget (OMB), Attn: Desk Officer for
EPA, 725 17th Street, Northwest,
Washington, DC 20503.
• Hand Delivery: Air and Radiation
Docket and Information Center, EPA/
DC, EPA West, Room 3334, 1301
Constitution Avenue, NW., Washington,
DC 20004. Such deliveries are only
accepted during the Docket Center’s
normal hours of operation, and special
arrangements should be made for
deliveries of boxed information.
Instructions: Direct your comments to
Docket ID No. EPA–HQ–OAR–2006–
0605. The EPA’s policy is that all
comments received will be included in
the public docket without change and
may be made available online at
www.regulations.gov, including any
personal information provided, unless
the comment includes information
claimed to be Confidential Business
Information (CBI) or other information
whose disclosure is restricted by statute.
Do not submit information that you
consider to be CBI or otherwise
protected through www.regulations.gov
or e-mail. The www.regulations.gov Web
site is an ‘‘anonymous access’’ system,
which means EPA will not know your
identity or contact information unless
you provide it in the body of your
comment. If you send an e-mail
comment directly to EPA without going
through www.regulations.gov your email address will be automatically
captured and included as part of the
comment that is placed in the public
docket and made available on the
Internet. If you submit an electronic
comment, EPA recommends that you
include your name and other contact
information in the body of your
comment and with any disk or CD–ROM
you submit. If EPA cannot read your
comment due to technical difficulties
and cannot contact you for clarification,
EPA may not be able to consider your
comment. Electronic files should avoid
the use of special characters, any form
of encryption, and be free of any defects
ADDRESSES:
ENVIRONMENTAL PROTECTION
AGENCY
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or viruses. For additional instructions
on submitting comments, go to section
I.B of the SUPPLEMENTARY INFORMATION
section of this document.
Docket: All documents in the docket
are listed in the www.regulations.gov
index. 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, will be publicly
available only in hard copy. Publicly
available docket materials are available
either electronically in
www.regulations.gov or in hard copy at
the Air and Radiation Docket and
Information Center, EPA/DC, EPA West,
Room 3334, 1301 Constitution Avenue,
Northwest, Washington, DC. The Public
Reading Room is open from 8:30 a.m. to
4:30 p.m., Monday through Friday,
excluding legal holidays. The telephone
number for the Public Reading Room is
(202) 566–1744, and the telephone
number for the Air and Radiation
Docket and Information Center is (202)
566–1742.
FOR FURTHER INFORMATION CONTACT: Mr.
Raghavendra (Raj) Rao, Air Quality
Policy Division, Office of Air Quality
Planning and Standards (C504–03),
Environmental Protection Agency,
Research Triangle Park, North Carolina
27711; telephone number (919) 541–
5344; fax number (919) 541–5509; email address: rao.raj@epa.gov or Dan
deRoeck, Air Quality Policy Division,
Office of Air Quality Planning and
Standards (C504–03), Environmental
Protection Agency, Research Triangle
Park, North Carolina 27711; telephone
number (919) 541–5593; fax number
(919) 541–5509; e-mail address:
deroeck.dan@epa.gov. To request a
public hearing or information pertaining
to a public hearing on this document,
contact Ms. Pamela S. Long, Air Quality
Policy Division, Office of Air Quality
Planning and Standards (C504–03),
Environmental Protection Agency,
Research Triangle Park, North Carolina
27711; telephone number (919) 541–
0641; fax number (919) 541–5509; email address: long.pam@epa.gov.
SUPPLEMENTARY INFORMATION:
I. General Information
A. Does this action apply to me?
Entities potentially affected by this
proposed action include owners and
operators of emission sources in all
industry groups, as well as the EPA and
State, local, and tribal governments that
are delegated authority to implement
these regulations. The majority of
sources potentially affected are expected
to be in the following groups:
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Category
NAICSa
Industry ..................................................................
Federal government ..............................................
221111, 221112, 221113, 221119, 221121,
221122.
32411 ....................................................................
325181, 32512, 325131, 325182, 211112,
325998, 331311, 325188.
32511, 325132, 325192, 325188, 325193,
32512, 325199.
32552, 32592, 32591, 325182, 32551 .................
211112 ..................................................................
48621, 22121 .......................................................
32211, 322121, 322122, 32213 ...........................
322121, 322122 ...................................................
336111, 336112, 336712, 336211, 336992,
336322, 336312, 33633, 33634, 33635,
336399, 336212, 336213.
325411, 325412, 325413, 325414 .......................
924110 ..................................................................
State/local/tribal Government ................................
924110 ..................................................................
a North
Industry group
Electric services.
Petroleum refining.
Industrial inorganic chemicals.
Industrial organic chemicals.
Miscellaneous chemical products.
Natural gas liquids.
Natural gas transport.
Pulp and paper mills.
Paper mills.
Automobile manufacturing.
Pharmaceuticals.
Administration of Air and Water Resources and Solid Waste Management
Programs.
Administration of Air and Water Resources and Solid Waste Management
Programs.
American Industry Classification System.
This table is not intended to be
exhaustive, but rather provides a guide
for readers regarding entities likely to be
regulated by this action. To determine
whether your facility is regulated by this
action, you should examine the
applicability criteria in the PSD rules for
attainment areas (40 CFR 52.21). If you
have any questions regarding the
applicability of this action to a
particular entity, contact the person
listed in the preceding FOR FURTHER
INFORMATION CONTACT section.
B. What should I consider as I prepare
my comments for EPA?
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1. Submitting CBI. Do not submit this
information to EPA through
www.regulations.gov or e-mail. Clearly
mark the part or all of the information
that you claim to be CBI. For CBI
information in a disk or CD ROM that
you mail to EPA, mark the outside of the
disk or CD ROM as CBI and then
identify electronically within the disk or
CD ROM the specific information that is
claimed as CBI. In addition to one
complete version of the comment that
includes information claimed as CBI, a
copy of the comment that does not
contain the information claimed as CBI
must be submitted for inclusion in the
public docket. Information so marked
will not be disclosed except in
accordance with procedures set forth in
40 CFR part 2. Send or deliver
information identified as CBI only to the
following address: Roberto Morales,
OAQPS Document Control Officer
(C404–02), Environmental Protection
Agency, Research Triangle Park, NC
27711, Attention Docket ID No. EPA–
HQ–OAR–2006–0605.
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2. Tips for Preparing Your Comments.
When submitting comments, remember
to:
• Identify the rulemaking by docket
number and other identifying
information (subject heading, Federal
Register date and page number).
• Follow directions—The agency may
ask you to respond to specific questions
or organize comments by referencing a
Code of Federal Regulations (CFR) part
or section 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.
• If you estimate potential costs or
burdens, explain how you arrived at
your estimate in sufficient detail to
allow for it to be reproduced.
• 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.
C. Where can I get a copy of this
document and other related
information?
In addition to being available in the
docket, an electronic copy of this
proposal will also be available on the
World Wide Web. Following signature
by the EPA Administrator, a copy of this
notice will be posted in the regulations
and standards section of our NSR home
page located at https://www.epa.gov/nsr.
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D. How can I find information about a
possible Public Hearing?
Persons interested in presenting oral
testimony should contact Ms. Pamela
Long, New Source Review Group, Air
Quality Policy Division (C504–03),
Environmental Protection Agency,
Research Triangle Park, NC 27711;
telephone number (919) 541–0641 or email long.pam@epa.gov at least 2 days
in advance of the public hearing.
Persons interested in attending the
public hearing should also contact Ms.
Long to verify the time, date, and
location of the hearing. The public
hearing will provide interested parties
the opportunity to present data, views,
or arguments concerning these proposed
rules.
The information presented in this
preamble is organized as follows:
I. General Information
A. Does this action apply to me?
B. What should I consider as I prepare my
comments for EPA?
C. Where can I get a copy of this document
and other related information?
D. How can I find information about a
possible Public Hearing?
II. Overview of Proposed Regulations
A. Summary of Proposed Options for
Increments
B. Summary of Proposed Options for SILs
C. Summary of Proposed Options for the
PM2.5 SMC
III. Background
A. PSD Program
B. History of PM NAAQS
1. TSP and PM10 NAAQS
2. PM2.5 NAAQS
3. Revised PM2.5 and PM10 NAAQS
C. Implementation of NSR for PM2.5
D. Background on Implementation of PSD
Increments
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E. Historical Approaches for Developing
Increments
1. Congressional Enactment of Increments
for PM and SO2.
2. EPA’s promulgation of increments for
NO2 and PM10
a. Increments for NOX Using the
‘‘Contingent Safe Harbor’’ Approach
Under Section 166(a) of the Act
b. Increments for PM10 Using ‘‘Equivalent
Substitution’’ Approach Under Section
166(f)
IV. EPA’s Interpretation of Section 166 of the
Clean Air Act
A. Which Criteria In Section 166 Should
EPA Use to Develop Increments for
PM2.5?
1. Support for ‘‘Contingent Safe Harbor’’
Approach for PM2.5 Under Section 166(a)
2. Support of ‘‘Equivalent Substitution’’
Approach for PM2.5 Under Section 166(f)
B. Requirements of Sections 166(a)–(d) of
the Clean Air Act
1. Regulations as a Whole Should Fulfill
Statutory Requirements
2. Contingent Safe Harbor Approach
3. The Statutory Factors Applicable Under
Section 166(c)
4. Balancing the Factors Applicable Under
Section 166(c)
5. Authority for States to Adopt
Alternatives to Increments
C. Requirements of Section 166(f) of the
Clean Air Act
V. Increments and Other Measures to Prevent
Significant Deterioration
A. Option 1—Contingent Safe Harbor
Approach for Annual and Short-Term
Increments—Section 166(a)
1. Proposed Framework for Pollutant
Specific PSD Regulations for PM2.5
a. Increment System
b. Area Classifications
c. Permitting Procedures
d. Air Quality Related Values Review by
Federal Land Manager and Reviewing
Authority
e. Additional Impacts Analysis
f. Installation of Best Available Control
Technology
2. Proposed Increments
a. Identification of Safe Harbor Increments
b. Data Utilized by EPA for the Evaluation
of the Safe Harbor Increments for PM2.5
c. Scope of Effects Considered
d. Evaluation of the Health and Welfare
Effects of PM2.5
e. Fundamental Elements of Increments
f. Evaluation of the Safe Harbor Increments
3. Proposed Baseline Dates for PM2.5
Increments Under Option 1
4. Revocation of PM10 Annual Increments
B. Option 2—Equivalent Substitution
Approach for Annual Increments—
Section 166(f)
1. Development of Equivalent Increments
2. Proposed Annual Increments for PM2.5
a. Option 2A
b. Option 2B
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3. Baseline dates
VI. Significant Impact Levels (SILs)
A. EPA’s Guidance on SILs in the PSD
Program
B. Legal Basis for SILs
C. Relationship of SILs to AQRVs
D. Proposed Options for PM2.5 SILs (for
PSD and NA–NSR)
1. Option 1. Propose SILs using the
approach we proposed for PM10 in 1996
2. Option 2. PM2.5 to PM10 Emissions Ratio
3. Option 3. PM2.5 to PM10 NAAQS Ratio
VII. Significant Monitoring Concentrations
(SMCs)
A. Background on SMCs
1. Preconstruction Monitoring and Its Role
in NSR Program
2. History of SMC Rules Adopted by EPA
B. Legal Basis for SMCs
C. Proposed Options for PM2.5 SMC
1. Option 1. Lowest Detectable
Concentration
2. Option 2. PM2.5 to PM10 Emissions Ratio
3. Option 3. PM2.5 to PM10 NAAQS Ratio
D. Correction of Cross References
VIII. Effective Date of the Final Rule, SIP
Submittal/Approval Deadlines and PM10
Revocation Deadline
A. Option 1: Increments promulgated
pursuant to section 166(a) of the Act.
1. Effective Date of Final Rule
2. State Program
3. Federal Program
B. Option 2: Increments Promulgated
Pursuant to Section 166(f) of the Act.
1. Effective date of Final Rule
2. State Program
3. Federal Program
C. Revocation of the PM10 Increment
D. Transition Period
E. Effective Date for SILs and SMCs
IX. Statutory and Executive Order Reviews
A. Executive Order 12866: Regulatory
Planning and Review
B. Paperwork Reduction Act
C. Regulatory Flexibility Act
D. Unfunded Mandates Reform Act
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 &
Safety Risks
H. Executive Order 13211: Actions That
Significantly Affect Energy Supply,
Distribution, or Use
I. National Technology Transfer and
Advancement Act
J. Executive Order 12898: Federal Actions
to Address Environmental Justice in
Minority Populations and Low-Income
Populations
X. Statutory Authority
PM2.5 increments, SILs, and a SMC. The
purpose of this proposed rulemaking is
to develop the final elements that will
aid implementation of the PSD program
for PM2.5. When final, these elements
will supplement the final NSR
implementation rule for PM2.5.
Following final action on this proposal
and the PM2.5 implementation rule for
NSR, the Federal PM2.5 NSR programs
will no longer have to rely on the PM10
program as a surrogate, as has been the
practice under our existing guidance. A
State implementing a NSR program in
an EPA approved State Implementation
Plan (SIP) may continue to rely on the
interim surrogate policy until we
approve a revised SIP addressing these
requirements. In this rulemaking, we 1
are proposing several options for
increments, SILs and the SMC,
respectively.
II. Overview of Proposed Regulations
This proposal is the first step in the
rulemaking process for promulgating
1 In this proposal, the terms ‘‘we,’’ ‘‘us,’’ and
‘‘our’’ refer to the EPA and the terms ‘‘you’’ and
‘‘your’’ refer to the owners or operators of stationary
sources of air pollution.
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A. Summary of Proposed Options for
Increments
We are proposing three sets of PM2.5
increments, based on several
approaches that are described in greater
detail later in this preamble. For the first
set (option 1), we are relying on an
approach that treats PM2.5 as a new
pollutant. This option follows our
statutory authority section 166(a) of the
Act to develop increments for
‘‘pollutants for which national ambient
air quality standards are promulgated
after the date of enactment of this part
* * * ’’ This is the same approach that
we used to establish NOX increment
regulations on October 12, 2005 (70 FR
at 59586). The second and third options
(options 2A and 2B) rely on an approach
that we used in 1993 to promulgate
PM10 increments in lieu of the statutory
increments for particulate matter (PM)
following our replacement of the then
existing indicator for the PM NAAQS
based on total suspended particulate
with a new indicator based on PM10. (58
FR 31622, June 3, 1993.) These two
options represent variations of the
approach used under the authority of
section 166(f) of the Act to ‘‘substitute’’
PM10 increments for TSP increments.
The increment values resulting from
each of these three options are:
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Proposed increments
(µg/m3)
Option
Class I
NAAQS
(µg/m3)
Class II
Class III
Annual
Annual
1 .......................................................................
2A .....................................................................
2B .....................................................................
B. Summary of Proposed Options for
SILs
We are also proposing three options
for SILs. The first option utilizes the
same approach we proposed for PM10 in
24-hr
1
1
1
Annual
2
2
2
24-hr
4
4
5
Annual
9
9
9
the 1996 NSR Reform proposal. For
option 2, we are proposing to scale the
PM10 SIL values by the ratio of direct
PM2.5 to direct PM10 emissions. The
PM2.5/PM10 emissions ratio is the
national average derived from the 2001
24-hr
................
15
................
................
35
................
24-hr
8
8
10
18
18
18
extrapolation of the 1999 National
Emissions Inventory. For option 3, we
are proposing to scale the PM10 SIL
values by the ratio of the PM2.5 NAAQS
to the PM10 NAAQS. The SIL values
resulting from each of these options are:
Proposed SILs
(µg/m3)
Option
Class I
Annual
1 ...............................................................................................................
2 ...............................................................................................................
3 ...............................................................................................................
C. Summary of Proposed Options for the
PM2.5 SMC
The first option we are proposing for
the SMC is the ‘‘Lowest Detection
Concentration’’ or LDC approach that
we used for establishing the SMC for
TSP and PM10. For option 2, we are
proposing to scale the PM10 SMC value
by the ratio of direct PM2.5 to direct
PM10 emissions. The PM2.5/PM10
emissions ratio is the national average
derived from the 2001 extrapolation of
the 1999 National Emissions Inventory.
For option 3, we are proposing to scale
the PM10 SMC value by the ratio of the
PM2.5 NAAQS to the PM10 NAAQS. The
proposed SMC values for each of these
options for the 24-hour averaging period
are:
Option 1—10 µg/m3
Option 2—7.9 µg/m3
Option 3—2.3 µg/m3
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III. Background
A. PSD Program
The NSR provisions of the Act are a
combination of air quality planning and
air pollution control technology
program requirements for new and
modified stationary sources of air
pollution. In brief, section 109 of the
Act requires us to promulgate primary
NAAQS to protect public health and
secondary NAAQS to protect public
welfare. Once we have set these
standards, States must develop, adopt,
and submit to us for approval SIPs that
contain emission limitations and other
control measures to attain and maintain
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0.04
0.16
0.06
Class II
24-hr
0.08
0.24
0.07
the NAAQS and to meet the other
requirements of section 110(a) of the
Act. Part C of title I of the Act contains
the requirements for a component of the
major new source review (NSR) program
known as the PSD program. This
program sets forth procedures for the
preconstruction review and permitting
of new and modified major stationary
sources of air pollution locating in areas
meeting the NAAQS (‘‘attainment’’
areas) and areas for which there is
insufficient information to classify an
area as either attainment or
nonattainment (‘‘unclassifiable’’ areas).
Most states have SIP-approved
preconstruction permit (major NSR)
programs. The Federal PSD program at
40 CFR 52.21 applies in some States that
lack a SIP-approved permit program,
and in Indian country.2 The
applicability of the PSD program to a
major stationary source must be
determined in advance of construction
and is a pollutant specific
determination. Once a major source is
determined to be subject to the PSD
program (PSD source), among other
requirements, it must undertake a series
of analyses to demonstrate that it will
use the best available control technology
(BACT) and will not cause or contribute
to a violation of any NAAQS or
incremental ambient pollutant
concentration increase (increment). In
2 We have delegated authority to some States to
implement the Federal PSD program. The EPA
remains the reviewing authority in non-delegated
States and in Indian country.
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Annual
1.0
0.8
0.3
Class III
24-hr
5.0
4.0
1.2
Annual
1.0
0.8
0.3
24-hr
5.0
4.0
1.2
cases where the source’s emissions may
adversely affect an area classified as a
Class I area, additional review is
conducted to protect the increments and
special attributes of such an area
defined as ‘‘air quality related values.’’
As part of the analysis of air quality
impacts to determine compliance with
the NAAQS and increment, the permit
applicant and reviewing authority may
compare the source’s impacts for a
pollutant with the corresponding SIL for
that pollutant to show that a cumulative
air quality impacts analysis is not
necessary. Similarly, the permit
applicant and reviewing authority may
use the corresponding SMC for that
pollutant to determine if pre-application
site-specific ambient monitoring data is
needed to conduct the air quality
analysis.
When the reviewing authority reaches
a preliminary decision to authorize
construction of each proposed major
new source or major modification, it
must provide notice of the preliminary
decision and an opportunity for
comment by the general public,
industry, and other persons that may be
affected by the emissions of the major
source or major modification. After
considering these comments, the
reviewing authority may issue a final
determination on the construction
permit in accordance with the PSD
regulations.
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B. History of PM NAAQS
revoked the annual PM10 NAAQS
(previously set at 50 µg/m3).
1. TSP and PM10 NAAQS
The EPA initially established NAAQS
for PM in 1971, measured by the TSP
indicator. Based on the size of the
particles collected by the ‘‘high-volume
sampler,’’ which was the reference
method for determining ambient
concentrations, TSP included all PM up
to a nominal size of 25 to 45
micrometers. We established both
annual and 24-hour NAAQS for TSP.
On July 1, 1987, we promulgated new
NAAQS for PM in which we changed
the indicator from TSP to PM10, the
latter including particles with a mean
aerodynamic diameter less than or equal
to 10 micrometers. These smaller
particles are the subset of inhalable
particles small enough to penetrate to
the thoracic region (including the
tracheobronchial and alveolar regions)
of the respiratory tract (referred to as
thoracic particles). We established
annual and 24-hour NAAQS for PM10,
and revoked the NAAQS for TSP. (52 FR
24634).
2. PM2.5 NAAQS
On July 18, 1997, we again revised the
NAAQS for PM in several respects.
While we determined that the NAAQS
should continue to focus on particles
less than or equal to 10 micrometers in
diameter, we also determined that the
fine and coarse fractions of PM10 should
be considered separately. We
established new annual and 24-hour
NAAQS for PM2.5 (referring to particles
with a nominal mean aerodynamic
diameter less than or equal to 2.5
micrometers) as the indicator for fine
particles. Our 1997 rules also modified
the PM10 NAAQS for the purpose of
regulating the coarse fraction of PM10
(referred to as thoracic coarse particles
or coarse-fraction particles; generally
including particles with a nominal
mean aerodynamic diameter greater
than 2.5 micrometers and less than or
equal to 10 micrometers, or PM10¥2.5),
however this part of the action was
vacated during subsequent litigation,
leaving the pre-existing 1987 PM10
NAAQS in place (62 FR 38652).
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3. Revised PM2.5 and PM10 NAAQS
On October 17, 2006, we promulgated
revisions to the NAAQS for PM2.5 and
PM10 with an effective date of December
18, 2006 (71 FR 61144). We lowered the
24-hour NAAQS for PM2.5 from 65
micrograms per cubic meter (µg/m3) to
35 µg/m3, and retained the existing
annual PM2.5 NAAQS of 15 µg/m3. In
addition, we retained the existing PM10
24-hour NAAQS of 150 µg/m3, and
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C. Implementation of NSR for PM2.5
After we established new annual and
24-hour NAAQS for PM2.5 (referring to
particles with a nominal mean
aerodynamic diameter less than or equal
to 2.5 micrometers) as the indicator for
fine particles in July 1997, we issued a
guidance document ‘‘Interim
Implementation for the New Source
Review Requirements for PM2.5,’’ John
S. Seitz, Director, Office of Air Quality
Planning and Standards, EPA, October
23, 1997. As noted in that guidance,
section 165 of the Act implies that PSD
requirements become effective for a new
NAAQS upon the effective date of the
NAAQS. Section 165(a)(1) of the Act
provides that no new or modified major
source may be constructed without a
PSD permit that meets all of the section
165(a) requirements with respect to the
regulated pollutant. Moreover, section
165(a)(3) provides that the emissions
from any such source may not cause or
contribute to a violation of any
increment or NAAQS. Also, section
165(a)(4) requires BACT for each
pollutant subject to PSD regulation. The
1997 guidance stated that sources would
be allowed to use implementation of a
PM10 program as a surrogate for meeting
PM2.5 NSR requirements until certain
difficulties were resolved. These
difficulties included the lack of
necessary tools to calculate the
emissions of PM2.5 and related
precursors, the lack of adequate
modeling techniques to project ambient
impacts, and the lack of PM2.5
monitoring sites.
On April 5, 2005, we issued a
guidance document entitled
‘‘Implementation of New Source Review
Requirements in PM–2.5 Nonattainment
Areas,’’ Stephen D. Page, Director,
Office of Air Quality Planning and
Standards, EPA. This memorandum
provides guidance on the
implementation of the nonattainment
major NSR provisions in PM2.5
nonattainment areas in the interim
period between the effective date of the
PM2.5 NAAQS designations (April 5,
2005) and when we promulgate
regulations to implement nonattainment
major NSR for the PM2.5 NAAQS. In
addition to affirming the continued use
of the John S. Seitz guidance memo in
PM2.5 attainment areas, this memo
recommends that until we promulgate
the PM2.5 major NSR regulations, States
should use a PM10 nonattainment major
NSR program as a surrogate to address
the requirements of nonattainment
major NSR for the PM2.5 NAAQS.
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On November 1, 2005, we proposed a
rule to implement the PM2.5 NAAQS,
including proposed revisions to the NSR
program. For those States with EPAapproved PSD programs, we proposed
to continue the 1997 NSR guidance to
use PM10 as a surrogate for PM2.5, but
only during the SIP development
period. We also indicate in that
proposal that we will develop
increments, SILs, and SMC in a separate
rulemaking—i.e. this proposed
rulemaking. Since there was an interim
surrogate NSR program in place, EPA
decided to first promulgate the non-NSR
part of the implementation rule
(including attainment demonstrations,
designations, control measures etc.)—
which was promulgated on April 25,
2007. The NSR part of the
implementation rule is anticipated to be
promulgated in September 2007.
Additionally, once this proposed
rulemaking is finalized, States will be
able to fully implement a PM2.5 NSR
program.
D. Background on Implementation of
PSD Increments
Under section 165(a)(3) of the Act, a
PSD permit applicant must demonstrate
that emissions from the proposed
construction and operation of a facility
‘‘will not cause, or contribute to, air
pollution in excess of any (A) maximum
allowable increase or maximum
allowable concentration for any
pollutant. * * *’’ 42 U.S.C. 7475(a)(3).
The ‘‘maximum allowable increase’’ of
an air pollutant that is allowed to occur
above the applicable baseline
concentration for that pollutant is
known as the PSD increment. By
establishing the maximum allowable
level of ambient pollutant concentration
increase in a particular area, an
increment defines ‘‘significant
deterioration.’’
For PSD baseline purposes, a baseline
area for a particular pollutant emitted
from a source includes the attainment or
unclassifiable area in which the source
is located as well as any other
attainment or unclassifiable area in
which the source’s emissions of that
pollutant are projected (by air quality
modeling) to result in an ambient
pollutant increase of at least 1 µg/m3
(annual average). See, e.g., 40 CFR
52.21(b)(15)(i). Once the baseline area is
established, subsequent PSD sources
locating in that area need to consider
that a portion of the available increment
may have already been consumed by
previous emissions increases.
In general, the submittal date of the
first complete PSD permit application in
a particular area is the operative
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‘‘baseline date.’’ 3 On or before the date
of the first complete PSD application,
emissions generally are considered to be
part of the baseline concentration,
except for certain emissions from major
stationary sources, as explained in the
following discussion of baseline dates.
Most emissions increases that occur
after the baseline date will be counted
toward the amount of increment
consumed. Similarly, emissions
decreases after the baseline date restore
or expand the amount of increment that
is available.
In practice, three dates related to the
PSD baseline concept are important in
understanding how to calculate the
amount of increment consumed—(1)
Trigger date; (2) minor source baseline
date; and (3) major source baseline date.
Chronologically, the first relevant date
is the trigger date. The trigger date, as
the name implies, triggers the overall
increment consumption process
nationwide. Specifically, this is a fixed
date, which must occur before the minor
source baseline date can be established
for the pollutant-specific increment in a
particular attainment area. See, e.g., 40
CFR 52.21(b)(14)(ii). For PM and SO2,
Congress defined the applicable trigger
date as August 7, 1977—the date of the
1977 amendments to the Act when the
original statutory increments were
established by Congress. For NO2, we
selected the trigger date as February 8,
1988—the date on which we proposed
increments for NO2. See 53 FR 40656,
40658; October 17, 1988. In this action,
as described later, we are proposing to
add a new trigger date for purposes of
calculating the new PM2.5 increments.
The two remaining dates—‘‘minor
source baseline date’’ and ‘‘major source
baseline date’’—as described later, are
necessary to properly account for the
emissions that are to be counted toward
increment consumed following the
national trigger date, in accordance with
the statutory definition of ‘‘baseline
concentration’’ in section 169(4) of the
Act. The statutory definition provides
that the baseline concentration of a
pollutant for a particular baseline area is
generally the air quality at the time of
the first application for a PSD permit in
the area. Consequently, any increases in
actual emissions occurring after that
date (with some possible exceptions that
we will discuss later) would be
considered to consume the applicable
PSD increment. However, the statutory
3 Baseline dates are pollutant specific. That is, a
complete PSD application establishes the baseline
date only for those regulated NSR pollutants that
are projected to be emitted in significant amounts
(as defined in the regulations) by the applicant’s
new source or modification. Thus, an area may have
different baseline dates for different pollutants.
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definition in section 169(4) also
provides that ‘‘[E]missions of sulfur
oxides and particulate matter from any
major emitting facility on which
construction commenced after January
6, 1975 shall not be included in the
baseline and shall be counted in
pollutant concentrations established
under this part.’’
To make this distinction between the
date when emissions changes in general
(i.e., from both major and minor
sources) affect the increment and the
date when emissions resulting from the
construction at a major stationary source
consume the increment, we established
the terms ‘‘minor source baseline date’’
and ‘‘major source baseline date,’’
respectively. See 40 CFR 51.166(b)(14)
and 52.21(b)(14). Accordingly, the
‘‘minor source baseline date’’ is the date
on which the first complete application
for a PSD permit is filed in a particular
area. Any change in actual emissions
after that date affects the PSD increment
for that area.
The ‘‘major source baseline date’’ is
the date after which actual emissions
increases associated with construction
at any major stationary source affect the
PSD increment. In accordance with the
statutory definition of ‘‘baseline
concentration,’’ the PSD regulations
define a fixed date to represent the
major source baseline date for each
pollutant for which an increment exists.
Congress defined the major source
baseline date for the statutory
increments for PM and SO2 as January
6, 1975. For the NO2 increments, which
we promulgated in 1988 under our
authority to establish an increment
system under section 166(a) of the Act,
the major source baseline date we
selected is February 8, 1988—the date
on which we proposed increments for
NO2. 53 FR 40656. In this action, as
described later, we are proposing to add
a new major source baseline date for
PM2.5.
The PSD regulations set out the third
date that is relevant to the PSD baseline
concept. These regulations provide that
the earliest date on which the minor
source baseline date can be established
is the date immediately following the
‘‘trigger date’’ for the pollutant-specific
increment. See, e.g., 40 CFR
52.21(b)(14)(ii). For PM and SO2,
Congress defined the applicable trigger
date as August 7, 1977—the date of the
1977 amendments to the Act when the
original statutory increments were
established by Congress. For NO2, we
selected the trigger date as February 8,
1988—the date on which we proposed
increments for NO2. See 53 FR 40656,
40658; October 17, 1988.
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Once the minor source baseline date
associated with the first PSD permit
application for a proposed new major
stationary source or major modification
in an area is established, the new
emissions from that source consume a
portion of the increment in that area, as
do any subsequent actual emissions
increases that occur from any new or
existing source in the area. When the
maximum pollutant concentration
increase defined by the increment has
been reached, additional PSD permits
cannot be issued until sufficient
amounts of the increment are ‘‘freed up’’
via emissions reductions that may occur
voluntarily, e.g., via source shutdowns,
or via control requirements imposed by
the reviewing authority. Moreover, the
air quality in a region cannot deteriorate
to a level in excess of the applicable
NAAQS, even if all the increment has
not been consumed. Therefore, new or
modified sources located in areas where
the air pollutant concentration is near
the level allowed by the NAAQS may
not have full use of the amount of
pollutant concentration increase
allowed by the increment.
Under EPA guidance, the actual
increment analysis that a proposed new
or modified source undergoing PSD
review must complete depends on the
area impacted by the source’s new
emissions.4 We have also provided
approved air quality models and
guidelines for sources to use to project
the air quality impact of each pollutant
(over each averaging period) for which
an increment analysis must be done.5 In
addition, we established significant
impact levels for each pollutant under
the nonattainment major NSR program
that have also been used under the PSD
program to identify levels below which
the source’s modeled impact is regarded
as de minimis. See 40 CFR 51.165(b)
and part 51, appendix S, section III.A.
In the event that a source’s modeled
impacts of a particular pollutant are
below the applicable significant impact
level at all ambient air locations
modeled, i.e., de minimis everywhere,
EPA policy provides that no further
modeling analysis is required for that
pollutant. Our policy is that when a
preliminary screening analysis based on
the significant impact level is sufficient
to demonstrate that the source’s
4 We note that on June 6, 2007, we published a
notice of proposed rulemaking proposing to refine
several aspects of the increment calculation process
to clarify how States and regulated sources may
calculate increases in pollutant concentrations for
purposes of determining compliance with the PSD
increments. See 72 FR at 31372. When final, these
revisions will amend the PSD regulations at 40 CFR
51.166 and 52.21.
5 See EPA’s ‘‘Guideline on Air Quality Models’’
at 40 CFR part 51, appendix W.
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emissions will not cause or contribute to
a violation of the increment, there is no
need for a full impacts analysis
involving a cumulative evaluation of the
emissions from the proposed source and
other sources affecting the area.
Within the impact area of a source
that does have a significant impact,
increment consumption is calculated
using the source’s proposed emissions
increase, along with other emissions
increases or decreases of the particular
pollutant from sources in the area,
which have occurred since the minor
source baseline date established for that
area. (For major sources, emissions
increases or decreases that have
occurred since the major source baseline
date consume or expand increment.)
Thus, an emissions inventory of sources
whose emissions consume or expand
the available increment in the area must
be compiled. The inventory includes
not only sources located directly in the
impact area, but sources outside the
impact area that affect the air quality
within the impact area.
The inventory of emissions includes
emissions from increment-affecting
sources at two separate time periods—
the baseline date and the current period
of time. For each source that was in
existence on the relevant baseline date
(major source or minor source), the
inventory includes the source’s actual
emissions on the baseline date and its
current actual emissions. The change in
emissions over these time periods
represents the emissions that consume
increment (or, if emissions have gone
down, expand the available increment).
For sources constructed since the
relevant baseline date, all their current
actual emissions consume increment
and are included in the inventory.
When the inventory of emissions has
been compiled, computer modeling is
used to determine the change in
ambient concentration that will result
from these emissions when combined
with the proposed emissions increase
from the new major source or major
modification that is undergoing PSD
review. The modeling has generally
been guided by the ‘‘Guideline on Air
Quality Models’’ (40 CFR part 51,
appendix W), which includes
provisions on air quality models and the
meteorological data input into these
models. The model output (expressed as
a change in concentration) for each
relevant averaging period is then
compared to the corresponding
allowable PSD increment.
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E. Historical Approaches for Developing
Increments
1. Congressional Enactment of
Increments for PM and SO2
Congress established the first
increments defining significant
deterioration of air quality in the 1977
Amendments to the Act. These
amendments to the Act, among other
things, added subpart C to title I, setting
out the requirements for PSD. In section
163, Congress included numerical
increments for PM and sulfur dioxide
(SO2) for Class I, II, and III areas.
The three area classes are part of the
increment system originally established
by Congress. Congress designated Class
I areas (including certain national parks
and wilderness areas) as areas of special
national concern, where the need to
prevent deterioration of air quality is the
greatest. Consequently, the allowable
level of incremental change is the
smallest relative to the other area
classes, i.e., most stringent, in Class I
areas. The increments of Class II areas
are larger than those of Class I areas and
allow for a moderate degree of
emissions growth. For future
redesignation purposes, Congress
defined as Class III any existing Class II
area for which a State may desire to
promote a higher level of industrial
development (and emissions growth).
Thus, Class III areas are allowed to have
the greatest amount of pollutant
increase of the three area classes while
still achieving the NAAQS. There have
been no Class III redesignations to date.
In establishing these PSD increments,
Congress used the then-existing NAAQS
for those pollutants as the benchmark
for determining what constitutes
‘‘significant deterioration.’’ Congress
established the increments for PM as a
percentage of the then-existing PM
NAAQS. At the time the Act was
amended in 1977, the NAAQS for PM
were expressed in terms of ambient
concentrations of total suspended
particulate (TSP). Thus, EPA interpreted
the statutory increments for PM using
the same ambient ‘‘indicator.’’
2. EPA’s Promulgation of Increments for
NO2 and PM10
Congress also provided authority for
EPA to promulgate additional
increments and to update the original
PM increments created by statute. The
EPA has promulgated two regulations
pursuant to this authority.
a. Increments for NOX Using the
‘‘Contingent Safe Harbor’’ Approach
Under Section 166(a) of the Act
As enacted in 1977, subpart C of the
Act also included sections 166(a)
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through 166(e), which set out
requirements related to increments for
other pollutants. Section 166(a) requires
EPA to develop regulations to prevent
the significant deterioration of air
quality due to emissions of certain
named pollutants, and to develop such
regulations for any pollutants for which
NAAQS are subsequently promulgated.
Section 166(b) prescribes timelines for
the effective date of such regulations,
and for corresponding SIP submittals
and EPA approvals. Specifically,
regulations, including increments,
developed pursuant to section 166(a)
become effective 1 year after the date of
promulgation, and State plan revisions
containing the new regulations are to be
submitted to EPA for review within 21
months of promulgation. The same
provision then calls for EPA’s approval
or disapproval of the revised plan
within 25 months of promulgation. The
legislative history indicates that this 1year delay before the new PSD
requirements, including the new
increments, become effective is to allow
Congress an opportunity to review them
before States are required to implement
them. H.R. Conf. Rep. 95–564, at 151
(1977), 1977 U.S.C.C.A.N. 1502, 1532.
Section 166(c) and (d) set forth criteria
and goals that such regulations must
meet.
Based on section 166 of the Act, on
October 17, 1988, EPA promulgated
increments for nitrogen dioxide (NO2) to
prevent significant deterioration of air
quality due to emissions of NOX (53 FR
40656). The EPA based these increments
on percentages of the NAAQS in the
same way that Congress derived the
statutory increments for PM and SO2.
Those NO2 increments were challenged
in 1988 by the Environmental Defense
Fund (now Environmental Defense, or
‘‘ED’’) when ED filed suit in the U.S.
Court of Appeals for the District of
Columbia Circuit against the
Administrator (Environmental Defense
Fund, Inc. v. Reilly, No. 88–1882).
Environmental Defense successfully
argued that we failed to sufficiently
consider certain provisions in section
166 of the Act. The court remanded the
case to EPA ‘‘to develop an
interpretation of section 166 that
considers both subsections (c) and (d),
and if necessary to take new evidence
and modify the regulations.’’ See
Environmental Defense Fund v. EPA,
898 F.2d 183, 190 (D.C. Cir. 1990).
Section 166(c) of the Act requires the
PSD regulations to, among other things,
meet the goals and purposes set forth in
sections 101 and 160 of the Act. Section
166(d) requires these regulations be at
least as effective as the increments
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established for PM (in the form of TSP)
and SO2 in section 163 of the Act. The
court considered the NO2 increment
values determined using the percentageof-NAAQS approach as ‘‘safe harbor’’
increments which met the requirements
of section 166(d) of the Act. However,
the court also determined that EPA’s
reliance on such increment levels was
contingent upon our completing the
analyses required under section 166(c),
which provided that the final increment
values must address the goals of
sections 101 and 160 of the Act to
protect public health and welfare, parks,
and air quality related values (AQRVs) 6
and to ensure economic growth.
In response to the court’s decision, we
proposed rulemaking on increments for
NOX on February 23, 2005 (70 FR 8880)
and finalized the rule on October 12,
2005 (70 FR 59582). In the final rule, we
established our policy on how to
interpret and apply the requirements of
sections 166(c) and (d) of the Act. In
accordance with the court ruling, we
conducted further analyses (considering
the health and welfare effects of NOX)
and concluded that the existing NO2
increments were adequate to fulfill the
requirements of section 166(c). See 70
FR 59586 for our detailed analysis of
how pollutant regulations satisfy the
requirements of section 166 of the Act.
Hence, we retained the existing NO2
increments along with other parts of the
existing framework of pollutant-specific
PSD regulations for NOX. We also
amended the requirements of 40 CFR
51.166 to make it clear that States may
seek EPA approval of SIPs that utilize a
different approach than EPA used to
establish these NO2 increments. To
receive our approval of an alternative
program, a State must demonstrate that
its program satisfies the requirements of
sections 166(c) and 166(d) of the Act
and prevents significant deterioration of
air quality from emissions of NOX.7
6 The term ‘‘air quality related values’’ is not
defined in the Act, but the legislative history
provides that ‘‘The term ‘air quality related values’
of Federal lands designated as class I includes the
fundamental purposes for which such lands have
been established and preserved by the Congress and
the responsible Federal agency. For example, under
the 1916 Organic Act to establish the National Park
Service (16 U.S.C. 1), the purpose of such national
park lands ‘is to conserve the scenery and the
natural and historic objects and the wildlife therein
and to provide for the enjoyment of the same in
such manner and by such means as will leave them
unimpaired for the enjoyment of future
generations.’ ’’ S. Rep. No. 95–127 at 36 (1977)
7 Under the 2005 NO regulation, States can
X
adopt measures other than increments as long as
they can demonstrate that the measures selected
comply with the same criteria and goals of 166 (c)
and (d) of the Act that must be met for increments.
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b. Increments for PM10 Using
‘‘Equivalent Substitution’’ Approach
Under Section 166(f)
On October 5, 1989, we proposed new
PM10 increments. See 54 FR 41218.
Although section 163 did not expressly
define the existing statutory increments
for PM in terms of a specific indicator,
EPA reasoned that Congress’s
knowledge that TSP was the indicator
for the PM NAAQS, and that the TSP
standards were the starting point for the
increments levels when the increments
were established in 1977, meant that
TSP was also the appropriate measure
for the PM increments in section 163.
As a consequence, EPA believed that the
statutory PM increments could not
simply be administratively redefined as
PM10 increments, retaining the same
numerical values, following the revision
of the PM NAAQS. Rather, we stated
our belief that with the promulgation of
the PM10 NAAQS, EPA had both the
responsibility and the authority under
sections 166 and 301 of the Act to
promulgate new increments for PM to
be measured in terms of PM10. We
further concluded that promulgating
PM10 increments to replace, rather than
supplement, the statutory TSP
increments under section 163
represented the most sensible approach
for preventing significant deterioration
with respect to PM. See 54 FR 41220–
41221.
We promulgated PM10 increments to
replace the existing TSP increments on
June 3, 1993 (58 FR 31622). In the
interim between proposal and
promulgation, Congress enacted the
1990 Act Amendments. As part of these
Act Amendments, Congress amended
section 166 to add a new section 166(f).
This section specifically authorized EPA
to substitute PM10 increments for the
existing section 163 PM increments
based on TSP, provided that the
substituted increments are ‘‘of equal
stringency in effect’’ as the section 163
increments.
Thus, we were able to replace the TSP
increments under section 163 of the Act
using PM10 increments based directly on
the newly enacted authority under
section 166(f) of the Act. In the PM10
rule, we maintained the existing
baseline dates and baseline areas for PM
that had been previously established
using the TSP indicator. Also as
proposed, we promulgated PM10
increments developed based on an
approach we called the ‘‘equivalent to
statutory increments’’ approach. Under
this approach, we used the original TSP
increments as a benchmark for
calculating the PM10 increments,
thereby retaining roughly the same
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54119
limitations on future deterioration of air
quality as was allowed under the TSP
increments. In using this approach, we
considered the historical consumption
of TSP increment by a sample
population of permitted PSD sources,
and then determined the PM10
increments for each area classification
and averaging time that would provide
approximately the same percentage of
PM10 increment consumption, on
average, by the same population of
sources. Then, all future calculations of
increment consumption after the PM10
implementation date would be based on
PM10 emissions. See 58 FR 31622 and
31625.
IV. EPA’S Interpretation of Section 166
of the Clean Air Act
A. Which Criteria in Section 166 Should
EPA Use to Develop Increments for
PM2.5?
The EPA interprets section 166 of the
Act to give the Administrator the
discretion to use either the ‘‘contingent
safe harbor’’ approach or the
‘‘equivalent substitution’’ approach to
establish increments for PM2.5. Since
sections 166(a) and section 166(f)
contain or incorporate different criteria
for establishing PSD regulations
containing increments or other
measures, the interpretation that EPA
chooses to follow could have an impact
on the increments or other measures
that EPA adopts. Regulations
promulgated under section 166(a) must
be based on the criteria in section 166(c)
and 166(d). 42 U.S.C. 7476(c)–(d).
Regulations promulgated under section
166(f) must ‘‘be of equal stringency in
effect as those specific in the provisions
for which they are substituted.’’ 42
U.S.C. 7476(f). Furthermore, section
166(a) calls broadly for regulations,
which may include increments, whereas
section 166(f) addresses only
increments.
Section 166(a) provides authority for
EPA to promulgate additional pollutantspecific PSD regulations, which may
include increments, for the pollutants
specifically identified in that provision
plus additional pollutants for which
EPA may promulgate a NAAQS after a
specific date 42 U.S.C. 7476(a). The last
sentence of section 166(a) provides the
following:
In the case of pollutants for which national
ambient air quality standards are
promulgated after August 7, 1977, [the
Administrator] shall promulgate such
regulations not more than 2 years after the
date of promulgation of such standards.
Since EPA promulgated an additional
NAAQS for PM, based on the PM2.5
indicator, in 1997, one potential
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approach for developing increments for
PM2.5 is for EPA to promulgate these
increments under the authority of
section 166(a). Under this approach,
EPA would promulgate increments or
other measures for PM2.5 that satisfy the
standards set forth in subsections (c)
and (d) of section 166, as interpreted by
EPA in our recent rulemaking for
nitrogen oxides.
However, in light of the provisions in
section 163 and 166(f) of the Act that
address increments for TSP and PM10,
respectively, there is some ambiguity on
the question of the legal authority EPA
should rely upon to establish
increments for PM2.5. In 1993, EPA
construed section 166(f) to establish the
sole criteria for promulgation of a new
PM increment and thus did not base our
final PM10 increment on section 166(a)
of the Act. Considering sections 163,
166(a), and 166(f) together, an
alternative interpretation of these
provisions might be that Congress
intended that section 163 and 166(f)
alone cover PM. Under this reading,
EPA would promulgate additional
increments for particular matter based
on the section 163 increments and
166(f) of the Act, which are the only
provisions that specifically mention PM
and PSD increments. However, as
discussed later, it may also be possible
to read sections 166(a) and 166(f) in
harmony. Thus, we propose to adopt
one of the following legal theories to
support promulgation of increments for
PM2.5 using either of the two methods
that EPA used in prior rules to develop
PSD increments.
1. Support for ‘‘Contingent Safe Harbor’’
Approach for PM2.5 Under Section
166(a)
The EPA believes it is permissible to
interpret section 166(a) to apply to
PM2.5. Although EPA has generally
characterized the NAAQS for PM2.5 as a
NAAQS for a new indicator of PM, EPA
did not replace the PM10 NAAQS with
the NAAQS for PM2.5 in 1997. Rather,
EPA established an additional NAAQS
for PM2.5 as if it were a new pollutant,
even though EPA had already developed
air quality criteria for PM generally.
Thus, for purposes of section 166(a), the
addition of a NAAQS for PM2.5 is
functionally the same as establishing a
NAAQS for an additional pollutant after
1977.
We read section 166(a) to authorize
EPA to promulgate pollutant-specific
PSD regulations meeting the
requirements of sections 166(c) and
166(d) for any pollutant for which EPA
promulgates a NAAQS after 1977. Most
of the pollutants identified in section
166(a) (nitrogen oxides, photochemical
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oxidants, carbon monoxide) are
pollutants for which EPA had
established NAAQS in 1977 when
Congress adopted section 166 of the Act.
There was no need for Congress to list
other criteria pollutants, sulfur dioxide
and particular matter, in section 166(a)
because Congress had already
established increments for these
pollutants in section 163 of the Act. In
addition to requiring regulations for the
enumerated pollutants, Congress clearly
intended to authorize EPA to establish
additional pollutant-specific PSD
regulations, potentially containing
increments, for any additional
pollutants for which EPA promulgated a
NAAQS under section 109 of the Act.
Furthermore, because the Act refers to
pollutants for which EPA promulgates
NAAQS after 1977, and does not use the
phrase ‘‘additional pollutants’’ we
believe that Section 166(a) provides
authority for EPA to promulgate new
increments after revising an existing
NAAQS (including one first
promulgated before 1977), when we find
that such action is appropriate.
In our 1989 proposal on the PM10
increments, EPA construed section
166(a) to apply to PM10, even though
EPA regarded PM10 to be a new
indicator for PM. 58 FR 31623–24. Thus,
before the adoption of section 166(f),
EPA read the language of section 166(a)
to apply to the promulgation of
increments using a new indicator for
PM and did not limit the application of
section 166(a) to wholly new criteria
pollutants. Similarly, in the current
proposal, EPA believes it can continue
to interpret section 166(a) to apply to
the promulgation of an additional
increment for a new indicator of an
existing criteria pollutant since EPA
promulgated a NAAQS for a new
indicator of that pollutant after 1977.
Although EPA ultimately applied the
standard in section 166(f) as the sole
basis for our PM10 increments in 1993,
that provision does not necessarily
govern the situation EPA currently faces
with PM2.5. One could read section
166(f) to address only EPA’s authority to
substitute new PM increments for the
congressionally-established increments
for TSP rather than the distinct issue
now faced by EPA concerning the
promulgation of additional PM
increments for PM2.5 without
necessarily revoking existing
increments. Furthermore, the language
in section 166(f) could be read to limit
the scope of this provision to only
increments using the PM10 indicator.
Thus, section 166(f) may not necessarily
be applicable to the substitution of PM10
increments with PM2.5 increments.
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The EPA believes that section 166(a)
could apply to the adoption of new
increments, without the revocation of
existing increments. As reflected in the
2005 increments rule for NOX and the
court decision in EDF v. EPA, when
sections 166(a)–(d) apply, EPA is
obligated to evaluate which indicator or
form should be used in our pollutantspecific PSD regulations to meet these
requirements in the Act. Based on this
interpretation, we are proposing to use
a contingent safe harbor approach
(option 1) that involves first deriving
increment values based on percentage of
the NAAQS and then evaluating
whether alternative increments or
additional measures are necessary to
meet the criteria in section 166(c).
2. Support of ‘‘Equivalent Substitution’’
Approach for PM2.5 Under Section
166(f)
The EPA believes it is also
permissible for the Agency to construe
section 166(f) as a continuing grant of
authority for the Administrator to
update the increments for particular
matter whenever the Administrator
decides to adopt a new form of
particular matter as the indicator for the
NAAQS. Although the terms of section
166(f) of the Act appear to address PM10
alone, the overall intent of this
provision was to clarify that EPA had
the authority to update the original TSP
increments to reflect changes in the
NAAQS indicator. Language describing
the PM10 indicator was used in the Act
because this was the indicator for PM
that EPA was seeking to incorporate into
the PSD program at the time of the 1990
Amendments when section 166(f) was
adopted. However, we believe it is
reasonable to conclude that Congress
intended to authorize EPA to continue
updating the particular matter
increments contained in section 163 if
EPA promulgated a NAAQS for another
appropriate indicator for particular
matter.
We believe EPA is authorized to
promulgate increments for PM2.5 as a
substitute for the PM10 increments, as
well as the original TSP increments, so
long as the new increments for PM2.5 are
of ‘‘equal stringency in effect as those
specified in the provisions for which
they are substituted.’’ 42 U.S.C. 7476(f).
Based on this interpretation, we propose
two approaches (options 2A and 2B
discussed later) for developing PM2.5
increments that would meet the ‘‘equal
stringency in effect’’ standard contained
in section 166(f).
While we believe section 166(f) may
be construed to provide continuing
authority to ‘‘update’’ the increments for
PM to conform to the NAAQS, section
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166(f) describes a process in which EPA
would ‘‘substitute’’ one PM increment
for another. The language in section
166(f) does not address whether EPA
may adopt additional increments for
other PM indicators while retaining the
existing PM increments. In contrast,
section 166(a) does contain language
addressing the promulgation of PSD
regulations when EPA adds to the suite
of NAAQS. Thus, we construe section
166(a) to have the closest connection to
the task of adding, rather than the
substituting or replacing, PSD
increments for PM. As a result, for
purposes of establishing the proposed
24-hour PM2.5 increments, we propose
only one option—using the contingent
safe harbor approach described in
option 1—because we are not proposing
to replace the existing 24-hour PM10
increment with a new 24-hour PM2.5
increment, since we have retained the
24-hour PM10 NAAQS. However, we
also seek comment on whether we could
rely on section 166(f) to promulgate the
24-hour PM2.5 increments using the
same methodology as for the annual
PM2.5 increments described later, even
though the 24-hour PM10 NAAQS is not
being revoked.
The goals and purposes of the PSD
program set forth in section 160 are as
follows:
B. Requirements of Sections 166(a)–(d)
of the Clean Air Act
As described in our 2005 rule for
NOX, EPA’s interpretation of these
provisions is grounded on five central
elements. First, we read section 166 of
the Act to direct EPA to conduct a
holistic analysis that considers how a
complete system of regulations will
collectively satisfy the applicable
criteria, rather than evaluating one
individual part of a regulatory scheme
in isolation. Second, we use a
‘‘contingent safe harbor’’ approach
which calls for EPA to first establish the
minimum level of effectiveness
necessary to satisfy section 166(d) and
then to conduct further analysis to
determine if additional measures are
necessary to fulfill the requirements of
section 166(c). Third, we interpreted
section 166(c) of the Act to identify
eight statutory factors that EPA must
apply when promulgating pollutantspecific regulations to prevent
significant deterioration of air quality.
Fourth, we interpreted the requirements
to simultaneously satisfy each of these
factors to establish a balancing test in
cases where certain objectives may be at
odds with each other. Fifth, we
recognized that the requirements of
section 166 may be satisfied by adopting
other measures besides an increment
and that EPA may allow States to
demonstrate that alternatives to an
increment contained in a SIP meet the
requirements of sections 166(c) and
166(d).
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If we determine that section 166(a)
applies to PM2.5, we propose to follow
the interpretation of sections 166(a)–(d)
that we adopted in our most recent
increments rule for NOX. This
interpretation was upheld in a recent
court decision E.D. v. EPA, No. 05–1446
(June 19, 2007 DC Cir.). We summarize
the key elements of this interpretation
later, but a more detailed discussion can
be found in our October 2005 final rule
for NOX. 70 FR 59582.
In section 166(a) of the Act, Congress
directed EPA to develop pollutantspecific regulations to prevent
significant deterioration of air quality.
Congress further specified that such
regulations meet the following
requirements set forth in sections 166(c)
and 166(d):
(c) Such regulations shall provide specific
numerical measures against which permit
applications may be evaluated, a framework
for stimulating improved control technology,
protection of air quality values, and fulfill the
goals and purposes set forth in section 101
and section 160.
(d) The regulations * * * shall provide
specific measures at least as effective as the
increments established in section 163 [for
SO2 and PM] to fulfill such goals and
purposes, and may contain air quality
increments, emission density requirements,
or other measures.
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(1) To protect public health and welfare
from any actual or potential adverse effect
which in the Administrator’s judgment may
reasonably be anticipate[d] to occur from air
pollution or from exposures to pollutants in
other media, which pollutants originate as
emissions to the ambient air,
notwithstanding attainment and maintenance
of all national ambient air quality standards;
(2) To preserve, protect, and enhance the
air quality in national parks, national
wilderness areas, national monuments,
national seashores, and other areas of special
national or regional natural, recreational,
scenic, or historic value;
(3) To insure that economic growth will
occur in a manner consistent with the
preservation of existing clean air resources;
(4) To assure that emissions from any
source in any State will not interfere with
any portion of the applicable implementation
plan to prevent significant deterioration of air
quality for any other State; and
(5) To assure that any decision to permit
increased air pollution in any area to which
this section applies is made only after careful
evaluation of all the consequences of such a
decision and after adequate procedural
opportunities for informed public
participation in the decisionmaking process.
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1. Regulations as a Whole Should Fulfill
Statutory Requirements
Section 166(a) directs EPA to develop
pollutant-specific regulations to prevent
the significant deterioration of air
quality. Sections 166(c) and 166(d)
provide detail on the contents of those
regulations, but do not necessarily
require the same type of increment
system Congress created in section 163
of the Act. Thus, in order to develop
pollutant-specific regulations under
subsection (a), EPA must establish both
the overall regulatory framework for
those regulations (such as system of
increments) and fill details around that
framework (such as the level of the
increments). Thus, EPA interprets
section 166 to require that the entire
system of PSD regulations (the
framework and details) for a particular
pollutant must, as a whole, satisfy the
criteria in sections 166(c) and 166(d).
We propose to use the same approach to
establish pollutant-specific regulations
for PM2.5 under option 1 of this
proposal.
When we propose a framework
involving numerical increments under
section 166(a) of the Act, we do not look
at increments in isolation, but we also
consider how these increments work in
conjunction with other measures to
satisfy the statutory criteria. The other
measures that EPA may consider
include new measures proposed by EPA
for that pollutant or measures applicable
to other pollutants that EPA proposes to
apply to additional pollutants.
Examples of other measures are an area
classification system, AQRV review in
Class I areas, additional impacts
analysis, and control technology
requirements. This approach is
consistent with section 166(d), which
says that pollutant-specific PSD
regulations ‘‘may contain’’ increments
or ‘‘other measures.’’
2. Contingent Safe Harbor Approach
The EPA continues to view the
‘‘contingent safe harbor’’ approach to be
an appropriate methodology for
ensuring that our pollutant-specific PSD
regulations meet the requirements of
sections 166(c) and 166(d). Subsection
(c) of section 166 describes the kinds of
measures to be contained in the
regulations to prevent significant
deterioration of air quality called for in
section 166(a) and specifies that these
regulations are to ‘‘fulfill the goals and
purposes’’ set forth in sections 160 and
101 of the Act. Then, under subsection
(d), to ‘‘fulfill such goals and purposes,’’
EPA must promulgate ‘‘specific
measures at least as effective as the
increments established in section 7473
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of this title [section 163 of the Act].’’ 42
U.S.C. 7476. Thus, subsection (d) can be
construed to require that EPA identify a
minimum level of effectiveness, or safe
harbor, for the body of pollutant-specific
PSD regulations adopted under section
166. Subsection (c) may then be read to
require that EPA conduct further review
to determine whether, based on the
criteria in subsection (c), EPA’s
pollutant-specific PSD regulations
under section 166 should contain
measures that deviate from the
minimum ‘‘safe harbor’’ identified
under subsection (d). EPA construes
subsection (d) to require that the
measures be ‘‘at least as stringent’’ as
the statutory increments set forth in
section 163.
When EPA employs an increment and
area classification system in regulations
promulgated under section 166 of the
Act, we interpret the Act to require that
EPA, at minimum, establish increments
that are consistent with the statutory
increments established by Congress in
section 163 of the Act. Thus, we start by
identifying ‘‘safe harbor’’ increments for
each area classification (Class I, II, or III)
that are established (1) Using an
equivalent percentage of the NAAQS as
the statutory increments; (2) for the
same pollutants as the NAAQS; and (3)
for the same time period as the NAAQS.
We then conduct further review to
determine whether these ‘‘safe harbor’’
increments, in conjunction with existing
elements of the PSD program or
additional measures proposed under
section 166 to augment the increments,
sufficiently fulfill the criteria in
subsection (c) of section 166. In this
review, we weigh and balance the
criteria set forth in subsection (c) (and
the incorporated goals and purposes of
the Act in section 101 and the PSD
program in section 160) to determine
whether additional measures are needed
to satisfy the criteria in subsection (c).
3. The Statutory Factors Applicable
Under Section 166(c)
The EPA interprets section 166(c) of
the Act to establish eight factors to be
considered in the development of PSD
regulations for the pollutants covered by
this provision. These factors are three of
the four criteria listed in section 166(c)
and the five goals and purposes
identified in section 160 of the Act. The
three stand-alone criteria in section
166(c) indicate that PSD regulations for
specific pollutants should provide (1)
Specific numerical measures for
evaluating permit applications; (2) a
framework for stimulating improved
control technology; and (3) protection of
air quality values. 42 U.S.C. 7476(c).
The five goals and purposes in section
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160 are incorporated into the analysis
by virtue of the fourth criterion in
section 166(c), which directs that EPA’s
pollutant-specific PSD regulations
‘‘fulfill the goals and purposes’’ set forth
in sections 160 and 101 of the Act. We
construe the term ‘‘fulfill the goals and
purposes,’’ as used in section 166(c), to
mean that EPA should apply the goals
and purposes listed in section 160 as
factors applicable to pollutant-specific
PSD regulations established under
section 166. The Agency’s view is that
PSD measures that satisfy the specific
goals and purposes of section 160 also
satisfy the more general purposes and
goals identified in section 101 of the
Act.
4. Balancing the Factors Applicable
Under Section 166(c)
The EPA interprets the Act to
establish a balancing test among the
eight factors. Since, as discussed further
later, many of the factors can be
satisfied by using an increment
framework, when determining the
characteristics of numerical increments
themselves within that framework, EPA
focuses on balancing the goal to
promote economic growth with the
factors that direct us to protect: (1)
AQRVs; (2) the public health and
welfare from reasonably anticipated
foreseeable adverse effects; and (3) the
air quality in parks and special areas.
Section 166 of the Act authorizes EPA
to promulgate pollutant-specific PSD
regulations that satisfy each of the eight
factors. While these objectives are
generally complementary, there are
circumstances where some of the
objectives may be in conflict. In these
situations, some degree of balance or
accommodation is inherent in the
requirement to establish regulations that
satisfy all of these factors.
As discussed in our PSD regulations
for NOX, we believe this balancing test
derives primarily from the third goal
and purpose set forth in section 160.
Section 160(3) directs us to ‘‘insure that
economic growth will occur in a manner
consistent with the preservation of
existing clean air resources.’’ To some
extent, this goal of the PSD program in
section 160(3) more specifically
articulates the broader purpose of the
Act, described in section 101(b)(1) of the
Act, to ‘‘protect and enhance the quality
of the Nation’s air resources so as to
promote the public health and welfare
and the productive capacity of its
population.’’ 42 U.S.C. 7401(b)(1).
Sections 160(3) and 101(b)(1) are similar
in that both sections reflect the goal to
protect air quality and maximize
opportunities for economic growth.
Thus, in interpreting the meaning of
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section 160(3) when used as a factor
applicable under section 166(c), we also
consider the broader purpose of the Act
set forth in section 101(b)(1).
The need to balance the applicable
factors to achieve these objectives is also
supported by our interpretation of the
second goal in section 160(2) of the Act
to ‘‘protect public health and welfare.’’
The precise meaning of this goal in the
context of the PSD program is somewhat
ambiguous because it appears to mirror
the legal standards applicable to the
promulgation of the primary and
secondary NAAQS. Under section
109(b) of the Act, the primary NAAQS
must ‘‘protect the public health’’ with
an adequate margin of safety (section
109(b)(1)) and the secondary NAAQS
must ‘‘protect the public welfare from
any known or anticipated adverse
effects’’ associated with ambient
concentrations of the pollutant (section
109(b)(2)). The term ‘‘welfare’’ is
defined in the Act to include ‘‘effects on
soils, water, crops, vegetation, manmade materials, animals, wildlife,
weather, visibility, and climate.’’
Section 302(h) of the Act.
When applied as one of the factors
applicable to pollutant-specific PSD
regulations under section 166(c) of the
Act, we construe the goal in section
160(3) of the to ‘‘protect public health
and welfare’’ to mean EPA should
evaluate whether reasonably anticipated
adverse effects may occur as a result of
increases in ambient pollutant
concentrations to levels below the
NAAQS. If such effects may occur in
some areas of the country, then EPA
would establish PSD regulations that
protect public health and welfare
against those effects where they may
occur. However, we do not interpret the
PSD program to require regulations that
eliminate all negative effects that may
result from increases in pollution in
attainment areas.
The PSD program is, as its title
indicates, designed to prevent
‘‘significant deterioration’’ from a
baseline concentration. See S. Rep. 95–
127 at 11 (3 LH at 1385) (‘‘This
legislation defines ‘significant
deterioration’ in all clean air areas as a
specified amount of additional
pollution.* * * This definition is
intended to prevent any major decline
in air quality currently existing in clean
air areas.’’ (emphasis added)). Thus,
some decline in air quality (relative to
the baseline air quality concentration) is
permissible for any particular area of the
country that is currently achieving the
NAAQS, as long as it is not
‘‘significant.’’
When EPA employs an area
classification system in its section 166
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regulations, we generally weigh these
factors in each type of area (Class I,
Class II, and Class III). However, the
weight given to each factor may be more
or less, depending on the area involved
and the amount of deterioration deemed
‘‘significant’’ for that type of area. For
example, economic growth may be the
most important factor in a Class III area,
but our PSD regulations for such areas
should offer some level of protection for
existing clean air resources. In a Class
I area, our PSD regulations should allow
some level of economic growth, even
though preservation of existing clean air
resources may be the dominant factor
for these areas.
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5. Authority for States To Adopt
Alternatives to Increments
While section 166 of the Act
authorizes EPA to promulgate
increments for pollutants listed under
section 166(a), we also interpret the
section to authorize States to employ
approaches other than increments to
prevent significant deterioration of air
quality, so long as such an approach
otherwise meets the requirements of
sections 166(c) and 166(d). As described
earlier, we explained this interpretation
in the 2005 NOX increment rulemaking
whereupon we amended the PSD
regulations at 40 CFR 51.166 by adding
new paragraph (c)(2) to codify this
statutory authority (70 FR 59582,
October 12, 2005). However, in
establishing the new provision, the
language at paragraph (c)(2) reflected
the authority for States to adopt
alternative measures only with respect
to increments for NOX. In order to
clarify our interpretation that the
authority to adopt alternative measures
covers any pollutant listed in section
166(a), we are proposing in this action
to revise existing 40 CFR 51.166(c)(2) to
make it inclusive to applicable
pollutants rather than just NOX.
C. Requirements of Section 166(f) of the
Clean Air Act
If we decide to use the equivalent
substitution options in this proposal for
PM2.5, EPA proposes to interpret section
166(f) of the Act in the same manner
that the Agency interpreted that
provision in our 1993 rule for PM10. In
1993, EPA construed section 166(f) as
authorizing EPA to follow the path that
EPA laid out in our 1989 proposal for
developing equivalent increments for
PM measured as PM10. 58 FR 31626.
Thus, in our 1993 rulemaking, EPA
developed our PM10 increments using
the ‘‘equivalent to statutory increments’’
option that EPA described in our notice
of proposed rulemaking. The EPA did
not interpret the ‘‘equivalent stringency
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in effect’’ standard in section 166(f) to
require EPA to use the second approach
from the proposal, the ‘‘percentage of
NAAQS’’ approach that Congress had
originally used to establish TSP
increments. The Agency observed that if
Congress intended to require EPA to
update the TSP increments using a
straight percentage, Congress could have
easily revised the increments in section
163 instead of providing EPA discretion
to establish increments following the
standard provided in section 166(f). 58
FR 31626. The EPA thus construed
section 166(f) as providing EPA
discretion to determine appropriate
equivalent levels of PM10. Id. The EPA
identified equivalent levels by
developing a ratio based on a
comparison of the TSP and PM10
impacts of stationary sources. 58 FR
31627.
In this rulemaking, EPA proposes to
apply the same type of ratio approach to
establish equivalent increments for
PM10 under section 166(f) of the Act.
Since this ratio approach was the
foundation of EPA’s equivalency
method in the 1989 proposal, we believe
it is permissible, as we did in 1993, to
construe section 166(f) as authorizing
EPA to continue utilizing this approach
to establish equivalent increments for
PM.
In 1993, EPA disagreed with
commenters who recommended that
EPA consider welfare effects and
visibility impairments when
establishing PM10 increments under
section 166(f) for class I areas. The EPA
observed that there was no evidence
that Congress itself adopted increments
that would ensure specific levels of
welfare and visibility protection at each
Class I area throughout the nation. The
increments established by Congress did
not establish an absolute ceiling on air
quality, but rather limited the marginal
amount of deterioration in air quality
above a baseline concentration that
varies for each area, and thus permitted
each area with the same classification to
deteriorate in the same amount without
regard to its particular sensitivities as
compared to other areas with the same
classification. 58 FR 31625. The EPA
concluded that the PM10 increments
should be designed to protect each area
from large adverse changes in air quality
while the air quality related values
analysis was the main tool for protecting
specific ecologically-based attributes in
particular class I areas. Id.
In this rulemaking for PM2.5, we
maintain the view that the ‘‘equal
stringency in effect’’ language in section
166(f) does not require EPA to consider
welfare effects and visibility when
promulgating replacement increments
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54123
under that provision. However, as
reflected in our recent increments rule
for NOX, when promulgating PSD
increments under section 166(a),
welfare effects and visibility impacts are
factors in the contingent safe harbor
analysis under the criteria in sections
166(c) and 160 of the Act. Consistent
with our recent PSD regulations for
NOX, we continue to believe that
increments (whether promulgated under
section 166(a) or 166(f)) should be
designed to provide each area with a
basic level of protection from large
adverse changes in air quality without
necessarily reflecting the unique air
pollution sensitivities in each class I
area. The EPA considers welfare and
visibility impacts across the nation
when establishing increments under
section 166(a), but we continue to
believe that the Air Quality Related
Values (AQRV) review is the preferred
tool for identification and protection of
specific ecologically-based attributes
within particular class I areas. See 58 FR
31625.
V. Increments and Other Measures To
Prevent Significant Deterioration
In this action, EPA is proposing three
options for establishing increments for
PM2.5. The first option described uses
the ‘‘contingent safe harbor’’ approach
(using percentages of the NAAQS as our
initial basis) following section 166(a) of
the Act. The other two options are
variations of the section 166(f)
‘‘Equivalent Increment’’ approach. The
EPA is proposing option 1 as our
preferred option and seeking comments
on the other two options.
A. Option 1—Contingent Safe Harbor
Approach for Annual and Short-Term
Increments—Section 166(a)
Under the first option, we would
consider PM2.5 to be a new pollutant 8
for which a NAAQS was promulgated
after the date of enactment of subpart C,
and we would use the authority of
section 166(a) of the Act to develop new
increments for PM2.5. Using this option,
we are proposing to establish a system
of increments at the safe harbor level in
conjunction with the other measures
described as follows:
1. Proposed Framework for Pollutant
Specific PSD Regulations for PM2.5
Under this option, EPA proposes to
apply the same basic framework
reflected in our regulation for NOX in
8 In our review of the PM NAAQS, we concluded
that, because the fine and thoracic coarse
components of PM10 generally have different
sources, composition and formation processes, they
should be treated as separate pollutants. (OAQPS
SP, December 2005, page 3–1.)
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pollutant-specific PSD regulations for
PM2.5. Thus, we propose to adopt an
increment and area classification system
for PM2.5 and to apply an AQRV review
process to PM2.5 as well. As discussed
further later, EPA believes that many of
the factors applicable under section
166(c) are fulfilled by using this type of
framework for pollutant-specific PSD
regulations under section 166(a) of the
Act. For other factors, this framework of
regulations partially contributes to the
fulfillment of an applicable factor but
may not fully satisfy that factor. In these
instances, the details of our regulations
(such as the characteristics of the
increments themselves) are also
important and we evaluate the
effectiveness of the framework in
conjunction with more detailed
elements of our regulations. The EPA
believes our obligations under section
166(c) of the Act are satisfied when the
PSD regulations collectively satisfy the
factors applicable under 166(c) of the
Act.
a. Increment System
An increment is the maximum
allowable level of ambient pollutant
concentration increase that is allowed to
occur above the applicable baseline
concentration in a particular area. As
such, an increment defines ‘‘significant
deterioration.’’ Establishing an
increment system for PM2.5 will fulfill
two of the factors applicable under
section 166(c).
An increment-based program satisfies
the requirements under 166(c) to
provide ‘‘specific numerical measures
against which permit applications may
be evaluated.’’ Under section 165(a)(3)
of the Act, a permit applicant must
demonstrate that emissions from the
proposed construction and operation of
a facility ‘‘will not cause, or contribute
to, air pollution in excess of any (A)
maximum allowable increase or
maximum allowable concentration for
any pollutant.’’ 42 U.S.C. 7475(a)(3).
Once the baseline date associated with
the first proposed new major stationary
source or major modification in an area
is established, the new emissions from
that source consume a portion of the
increment in that area, as do any
subsequent emissions increases that
occur from any source in the area. When
the maximum pollutant concentration
increase defined by the increment has
been reached, additional PSD permits
cannot be issued until sufficient
amounts of the increment are ‘‘freed up’’
via emissions reductions that may be
required by the reviewing authority.
Thus, an increment is a quantitative
value that establishes a ‘‘maximum
allowable increase’’ for a particular
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pollutant. It functions, therefore, as a
specific numerical measure that can be
used to evaluate whether an applicant’s
proposed project will cause or
contribute to air pollution in excess of
allowable levels.
Increments also satisfy the second
factor in section 166(c) by providing ‘‘a
framework for stimulating improved
control technology.’’ Increments
establish an incentive to apply
improved control technologies in order
to avoid violating the increment and to
‘‘free-up’’ available increment to
promote continued economic growth.
These control technologies may become
the basis of BACT determinations
elsewhere, as the technologies become
more commonplace and the costs tend
to decline. See also S. Rep. 95–127 at
18, 30 (3 LH at 1392, 1404) (‘‘the
incremental ceiling should serve as an
incentive to technology, as a potential
source may wish to push the frontiers of
technology in a particular case to obtain
greater productive capacity within the
limits of the increments’’).
However, we recognize that an
increment system is not the only way to
fulfill the requirements of section 166 of
the Act. Congress did not require EPA
to utilize increments in our PSD
regulations for NOX but gave EPA the
discretion to employ increments if
appropriate to meet the criteria and
goals and purposes set forth in sections
166 and 160 of the Act. 42 U.S.C.
7474(d); EDF v. EPA, 898 F.2d at 185
(‘‘Congress contemplated that EPA
might use increments’’). Thus, in this
action, we are also proposing to allow
States to develop alternatives to an
increment system at their discretion,
and to submit any such alternative
program to EPA so that we can
determine whether it satisfies the
requirements of section 166.
b. Area Classifications
The EPA proposes to establish the
same three-tiered area classification
system for PM2.5 that is applicable to
NOX and other pollutants under the PSD
program and the Clean Air Act.
Accordingly, areas that are currently
Class I for other pollutants would also
be Class I for PM2.5 and all other areas
would be Class II for PM2.5 unless we
redesignated the area based on a request
by a state or tribe pursuant to the
process in section 164 of the Act and
EPA’s regulations at 40 CFR 51.166(g)
and 52.21(g).
As explained earlier, in section III.E.1,
Class I areas are areas where especially
clean air is most desirable. In contrast,
Class III areas, which are those areas in
which a State wishes to permit the
highest relative level of industrial
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development, have the largest increment
level. Areas that are not especially
sensitive or that do not wish to allow for
a higher level of industrial growth are
classified as Class II. When Congress
established this three-tiered scheme for
SO2 and PM, it intended that Class II
areas be subject to an increment that
allows ‘‘moderately large increases over
existing pollution.’’
H.R. Rep. 95–294, 4 LH at 2609.
Establishing increments at different
levels for each of the three area
classifications helps to fulfill two of the
factors applicable under section 166(c)
of the Act. Establishing the smallest
increments in Class I areas helps fulfill
EPA’s obligation to establish regulations
that ‘‘preserve, protect, and enhance the
air quality’’ in parks and special areas.
Class I areas are primarily the kinds of
parks and special areas covered by
section 160(2) of the Act. With the air
quality in Class I areas subject to the
greatest protection, this scheme then
provides two additional area
classifications with higher increment
levels to help satisfy the goal in section
160(3) of the Act that EPA ‘‘insure that
economic growth will occur in a manner
consistent with preservation of clean air
resources.’’ In those areas where clean
air resources may not require as much
protection, more growth is allowed. By
employing an intermediate level (Class
II areas) and higher level (Class III
areas), this classification scheme helps
ensure that growth can occur where it
is needed (Class III areas) without
putting as much pressure on existing
clean air resources in other areas where
some growth is still desired (Class II
areas).
By requesting that EPA redesignate an
existing Class II area to Class III, States
may accommodate economic growth
and air quality in areas where the Class
II increment is too small to allow the
siting of new or modified sources. The
procedures specified by the Act for such
a redesignation require a commitment
by the State government to create such
an area, extensive public review, local
government participation in the SIP area
redesignation process, and a finding that
the redesignation will not result in the
applicable increment being exceeded in
a nearby Class I or Class II area. See 42
U.S.C. 7474(a)–(b) (Section 164(a)–(b) of
the Act). The EPA believes that the
three-tiered classification system has
allowed for economic growth, consistent
with the preservation of clean air
resources.
However, an area classification
system alone may not completely satisfy
the factors applicable under section
166(c) of the Act. The increment that is
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employed for each class of area is also
relevant to an evaluation of whether the
area classification scheme achieves the
goals of the PSD program. We discuss
the characteristics of increments later.
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c. Permitting Procedures
Two of the factors applicable under
section 166(c) are fulfilled by the caseby-case permit review procedures that
are built into our existing regulations.
The framework of our existing PSD
regulations employs the preconstruction
permitting system and procedures
required under section 165 of the Act.
42 U.S.C. 7475. These requirements are
generally reflected in 40 CFR 51.166 and
52.21 of EPA’s PSD regulations in Title
40 of the Code of Federal Regulations.
These permitting and review
procedures, which we interpret to apply
to construction of new major sources
and to major modifications at existing
sources, fulfill the goals set forth in
sections 160(4) and 160(5) of the Act.
These goals require that PSD programs
in one State not interfere with the PSD
programs in other States and that PSD
programs assure that any decision to
permit increased air pollution is made
after careful evaluation and public
participation in the decisionmaking
process. For the same reasons discussed
in our proposal for the pollutantspecific PSD regulations for NOX
regulations, 70 FR 8896, we believe
these factors are also fulfilled for PM2.5
by employing the permit review
procedures.
d. Air Quality Related Values Review by
Federal Land Manager and Reviewing
Authority
The EPA also proposes to apply the
requirement to evaluate impacts on
AQRVs in Class I areas to PM2.5. The
AQRV review provides the Federal Land
Managers (FLM) the opportunity to
review source impacts on site-specific
AQRVs in Class I areas and to bring any
adverse impacts to the attention of the
reviewing authority. Under an
increment approach, we consider this
review to be an additional measure that
helps to satisfy the factors in sections
166(c) and 160(2) which require that
EPA’s pollutant-specific PSD
regulations protect air quality values,
and parks and other special areas,
respectively.
In our rulemakings addressing PSD
for NOX, EPA extended the AQRV
review procedures set forth in 40 CFR
51.166(p) and 52.21(p) to cover NO2.
These AQRV review procedures were
established based on section 165(d) of
the Act, and they were originally
applied only in the context of the
statutory increments for PM and SO2.
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However, because they also address
many of the factors applicable under
section 166(c) of the Act, EPA also
applied them to NOX through
regulation. We propose the same
approach for PM 2.5 in this rulemaking.
Section 165(d) creates a scheme in
which the FLM and reviewing authority
must review the impacts of a proposed
new or modified source’s emissions on
AQRVs. The Act assigns to the FLM an
‘‘affirmative responsibility’’ to protect
the AQRVs in Class I areas. The FLM
may object to or concur in the issuance
of a PSD permit based on the impact, or
lack thereof, that new emissions may
have on any affected AQRV that the
FLM has identified and for which
information is available to the general
public. If the proposed source’s
emissions do not cause or contribute to
a violation of a Class I increment, the
FLM may still prevent issuance of the
permit by demonstrating to the
satisfaction of the reviewing authority
that the source or modification will
have an adverse impact on AQRVs.
Section 165(d)(2)(C). On the other hand,
if the proposed source will cause or
contribute to a violation of a Class I
increment, the reviewing authority
(State or EPA) shall not issue the permit
unless the owner or operator
demonstrates to the satisfaction of the
FLM that there will be no adverse
impact on AQRVs.9 Thus, the
compliance with the increment
determines whether the FLM or the
permit applicant has the burden of
satisfactorily demonstrating whether or
not the proposed source’s emissions
would have an adverse impact on
AQRVs.10 In any event, the FLM plays
an important and material role by
raising these issues for consideration by
the reviewing authority, which in the
majority of cases will be the State.
Incorporating these AQRV review
procedures into the PSD regulations for
PM2.5 helps to provide protection for
parks and special areas (which are
generally the Class I areas subject to this
review) and air quality values (which
are factors considered in the review). As
discussed later, we believe the factors
9 Even
if such a waiver of the Class I increment
is allowed upon a finding of no adverse impact, the
source must comply with such emissions
limitations as may be necessary to ensure that the
Class II increment for SO2 or PM is not exceeded.
Section 165(d)(2)(C)(iv). The EPA made this
provision applicable to the PSD provisions for NOX,
with a cap of 25 g/m 3—the NO 2 Class II increment.
53 FR 3704; 40 CFR 51.166(p)(4) and 52.21(p)(5).
10 In response to concerns that Class I increment
would hinder growth in areas surrounding the Class
I area, Congress established Class I increments as a
means of determining where the burden of proof
should lie for a demonstration of adverse effects on
AQRVs. See Senate Debate, June 8, 1977 (3 LH at
725).
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applicable under section 166(c) of the
Act can be fulfilled when the review of
AQRVs is applied in conjunction with
increments and other aspects of our PSD
regulations. In those cases where the
increment is not violated and the
reviewing authority agrees that a
proposed project will adversely affect
AQRVs, the parks and other special
areas will be protected by denying
issuance of the permit or by requiring
the applicant to modify the project to
alleviate the adverse impact. Legislative
history suggests that the AQRV review
provisions of section 165(d) were
intended to provide another layer of
protection, beyond that provided by
increments. The Senate committee
report stated the following: ‘‘A second
test of protection is provided in
specified Federal land areas (Class I
areas), such as national parks and
wilderness areas; these areas are also
subjected to a review process based on
the effect of pollution on the area’s air
quality related values.’’ S. Rep. 95–127,
at 17, 4 LH at 1401. As we stated in the
NOX rule, we believe the term ‘‘air
quality values’’ should be given the
same meaning as ‘‘air quality related
values.’’ Legislative history indicates
that the term ‘‘air quality value’’ was
used interchangeably with the term ‘‘air
quality related value’’ (AQRV) regarding
Class I lands.11
e. Additional Impacts Analysis.
The additional impacts analysis set
forth in our regulations also helps fulfill
the criteria and goals and purposes in
sections 166(c) and 160. The additional
impacts analysis involves a case-by-case
review of potential harm to visibility,
soils, and vegetation that could occur
from the construction or modification of
a source.
Sections 51.166(o)(1) and 52.21(o)(1)
of the PSD regulations require that a
permit provide the following analysis:
An analysis of the impairment to visibility,
soils and vegetation that would occur as a
result of the source or modification, and
general commercial, residential, industrial
and other growth associated with the source
11 See S. Rep. 95–127, at 12, reprinted at 3 LH at
1386, 1410 (describing the goal of protecting ‘‘air
quality values’’ in ‘‘Federal lands—such as national
parks and wilderness areas and international
parks,’’ and in the next paragraph and subsequent
text using the term ‘‘air quality related values’’ to
describe the same goal); id. at 35, 36 (‘‘The bill
charges the Federal land manager and the
supervisor with a positive role to protect air quality
values associated with the land areas under the
jurisdiction of the [FLM]’’ and then describing the
statutory term as ‘‘air quality related values’’). H.R.
Report 95–564 at 532 (describing duty of
Administrator to consider ‘‘air quality values’’ of
the tribal and State lands in resolving an appeal of
a tribal or State redesignation, which is described
in the final bill as ‘‘air quality related values’’).
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or modification. The owner or operator need
not provide an analysis of the impact on
vegetation having no significant commercial
or recreational value.
This requirement was based on section
165(e)(3)(B) of the Act, which provides
that EPA establish regulations that
require ‘‘an analysis of the ambient air
quality, climate and meteorology,
terrain, soils and vegetation, and
visibility at the site of the proposed
major emitting facility and in the area
potentially affected by emissions from
such facility * * * ’’
42 U.S.C. 7475(e)(3)(B).
This portion of the additional impacts
analysis is especially helpful for
satisfying the requirements of section
166(c) in Class II and Class III areas.
These areas are not subject to the
additional AQRV review that applies
only in Class I areas. While not as
intensive a review as AQRV analysis
required in Class I areas, considering
impairments to visibility, soils, and
vegetation through the additional
impacts analysis contributes to
satisfying the factors applicable under
section 166(c) of the Act in all areas,
including Class II and Class III areas.
f. Installation of Best Available Control
Technology
The requirement that new sources and
modified sources subject to PSD apply
BACT is an additional measure that
helps to satisfy the factors in sections
166(c), 160(1), and 160(2) of the Act.
This requirement, based on section
165(a)(4) of the Act, is already included
in EPA’s PSD regulations and thus we
consider it to be a part of the regulatory
framework for the Agency’s pollutantspecific regulations for PM2.5. 40 CFR
52.21(j); 40 CFR 51.166(j). Our existing
regulations define ‘‘best available
control technology’’ as ‘‘an emission
limitation * * * based on the maximum
degree of reduction for each pollutant
subject to regulation under the Act
* * * which the Administrator, on a
case-by-case basis, taking into account
energy, environmental, and economic
impacts and other costs, determines is
achievable for such source through
application of production processes or
available methods, systems, and
techniques * * * ’’ 40 CFR 52.21(b)(12);
40 CFR 52.166(b)(12). This pollutant
control technology requirement in
practice has required significant
reductions in the pollutant emissions
increases from new and modified
sources while also stimulating the ongoing improvement of control
technology. The control of PM2.5
emissions through the application of
BACT helps to protect air quality
values, public health and welfare, and
parks and other special areas.
2. Proposed Increments
Based on our evaluation of the effects
of PM2.5 and a balancing of the criteria
in section 166(c) of the Act (and the
incorporated goals and purposes of the
Act in section 101 and the PSD program
in section 160), EPA proposes to find
that the ‘‘safe harbor’’ increments for
PM2.5 (which meet the minimum
requirements in section 166(d) of the
Act) are sufficient to fulfill the criteria
in section 166(c) when combined with
the other measures described earlier that
we propose to apply to PM2.5. Since
several of the eight factors applicable
under section 166(c) are satisfied by
adopting the framework and other
measures described earlier, our
development of the proposed
increments for PM2.5 was guided by the
four remaining factors that may not be
fully satisfied by the framework and
other measures: (1) Protecting AQRVs;
(2) protecting the public health and
welfare from reasonably-anticipated
adverse effects; (3) protecting the air
quality in parks and special areas; and
(4) ensuring economic growth.12 In
accordance with the contingent safe
harbor approach, to determine the
specific characteristics of the proposed
increments, we first established the
minimum level of effectiveness
necessary to satisfy section 166(d) and
then conducted further analysis to
determine if additional measures are
necessary to fulfill the requirements of
section 166(c).
a. Identification of Safe Harbor
Increments
Using the percentage-of-NAAQS
approach, we derived the following safe
harbor increments for PM2.5:
Increments
(µg/m 3)
NAAQS
(µg/m 3)
Averaging period
Class I
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Annual ..............................................................................................................................................
24-hour .............................................................................................................................................
15
35
Class II
1
2
Class III
4
9
8
18
The PM2.5 levels of both the primary
and secondary NAAQS are 15 µg/m 3 for
the annual averaging time and 35 µg/m 3
for the 24-hour averaging time. See 40
CFR 50.7. We calculated the safe harbor
increments based on the same
percentages that were used by Congress
to establish the original PM increments
(measured as TSP) in section 163 of the
Act i.e. 6.6 percent of the NAAQS for
Class I areas; 25 percent of the NAAQS
for Class II areas and 50 percent of the
NAAQS for Class III areas. Increments
with these characteristics are sufficient
to satisfy the requirement in section
166(d) requirement that we adopt
We evaluated whether measures other
than the safe harbor increments are
necessary by analyzing primarily the
scientific and technical information on
the health and welfare effects of PM2.5
contained in the June 2005 OAQPS Staff
Paper (SP) used for the periodic review
of the 2004 PM air quality Criteria
Document (CD).13
Section 166 provides that EPA is to
establish pollutant-specific PSD
regulations, including increments, after
the establishment of a NAAQS for the
applicable pollutants. 42 U.S.C. 7476(a).
Under normal circumstances, the Act
provides that EPA promulgate new PSD
regulations under section 166, including
new increments if appropriate, within 2
years from the promulgation of any
NAAQS after 1977. 42 U.S.C. 7476(a). In
such instances, the health and welfare
information used for the setting of the
NAAQS would also be ‘‘current’’ for
12 We have paraphrased these factors here and in
other sections to facilitate the explanation of our
reasoning. However, we recognize, as we did in our
regulation for NOX that the statutory language is
broader than the shorthand we use here for
convenience.
13 This periodic review of the PM NAAQS
updates the last review, which began in 1994 and
resulted in revised standards for PM in 1997.
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increments (or other PSD regulations)
that are ‘‘at least as effective as’’ the
increments established in section 163 of
the Act. 42 U.S.C. 7476(d); See EDF v.
EPA, 898 F.2d at 188, 190.
b. Data Utilized by EPA for the
Evaluation of the Safe Harbor
Increments for PM2.5
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purposes of establishing pollutantspecific PSD regulations. We believe
this timing reflects Congressional intent
that EPA consider the same body of
information concerning a pollutant’s
health and welfare effects when it
promulgates the NAAQS and
subsequent PSD increments (or other
measures) defining significant air
quality deterioration for the same
pollutant. However, when we use that
same information as the basis for our
pollutant-specific PSD regulations, we
must evaluate that information under
the legal criteria in section 166 of the
Act rather than the criteria in section
109 applicable to the promulgation of
NAAQS. See EDF v. EPA, 898 F.2d at
190.
Since we just completed a review of
the PM 2.5 NAAQS, the information used
in that review is current and timely for
purposes of this proposal to establish
pollutant-specific PSD regulations for
PM2.5. As discussed earlier, on October
17, 2006, based primarily on
considerable new data on the air quality
and human health effects for PM2.5
directly, EPA revised the primary and
secondary NAAQS to provide increased
protection of public health and welfare
by retaining the level of the annual
standard and tightening the level of the
24-hour standard from 65 to 35 µg/m 3
while retaining the 24-hour PM10
NAAQS and revoking the annual PM10
NAAQS. The information contained in
the 2004 CD and 2005 SP that we also
consider for purposes of this proposed
rule was used for this latest review of
the PM NAAQS.
The 2004 CD and 2005 SP are the
products of a rigorous process that is
followed to validate and interpret the
available scientific and technical
information, and provided the basis for
recommending the PM2.5 NAAQS. In
accordance with the Act, the NAAQS
process begins with the development of
‘‘air quality criteria’’ under section 108
for air pollutants that ‘‘may reasonably
be anticipated to endanger public health
or welfare’’ and that come from
‘‘numerous or diverse’’ sources. Section
108(a)(1). For each NAAQS review, the
Administrator must appoint ‘‘an
independent scientific review
committee composed of seven members
of the National Academy of Sciences,
one physician, and one person
representing State air pollution control
agencies,’’ known as the Clean Air
Scientific Advisory Committee
(CASAC). Section 109(d)(2)(A). The
CASAC is charged with recommending
revisions to the criteria document and
NAAQS, and advising the Administrator
on several issues, including areas in
which additional knowledge is required
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to appraise the adequacy and basis of
existing, new, or revised NAAQS.
Section 109(d)(2)(B),(C).
‘‘Air quality criteria ’’ must reflect the
latest scientific knowledge on ‘‘all
identifiable effects on public health or
welfare ’’ that may result from a
pollutant’s presence in the ambient air.
42 U.S.C. 7408(a)(2). The scientific
assessments constituting air quality
criteria generally take the form of a
‘‘criteria document,’’ a rigorous review
of all pertinent scientific studies and
related information. The EPA also
develops a ‘‘staff paper ’’ to ‘‘bridge the
gap’’ between the scientific review and
the judgments the Administrator must
make to set standards. See Natural
Resources Defense Council v. EPA
(‘‘NRDC’’), 902 F.2d 962, 967 ‘‘D.C. Cir.
1990). Both documents undergo
extensive scientific peer-review as well
as public notice and comment. See, e.g.,
62 FR 38654/1–2.
c. Scope of Effects Considered
The effects of ambient PM2.5
concentrations may include
secondarily-formed PM2.5. Hence, in
this analysis we have evaluated the
health and welfare effects of both direct
PM2.5 and secondarily-formed PM2.5 that
may result from the transformation of
other pollutants such as SO2 and NOX.
This is consistent with the approach we
described for addressing these effects in
the recently completed review of our
pollutant-specific PSD regulations for
NOX. 70 FR 59590.
d. Evaluation of the Health and Welfare
Effects of PM2.5
Airborne PM is not a specific
chemical entity, but rather is a mixture
of liquid and solid particles from
different sources and of different sizes,
compositions and properties. Particle
size distributions show that atmospheric
particles exist in two classes: fine
particles and coarse particles. PM2.5 is
an indicator for fine particles and
represents particles that are mostly less
than 2.5 micrometers in size. PM10–2.5 is
an indicator for thoracic coarse particles
and represents particles sized between
2.5 and 10 micrometers. In the last two
reviews of the PM NAAQS, EPA
concluded that these two indicators,
because of their different sources,
composition, and formation processes
should be treated as separate subclasses
of PM pollution for purposes of setting
ambient air quality standards.
Coarse particles are generally primary
particles, emitted directly from their
source as particles. These particles
result from mechanical disruption of
large particles by crushing or grinding,
from evaporation of sprays, or from dust
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resuspension. In addition, some
combustion-generated particles may be
found as coarse particles. By
comparison, fine PM is derived directly
from combustion material that has
volatilized and then condensed to form
primary PM or from precursor gases,
such as SO2 and NOX, reacting in the
atmosphere to form secondary PM.
Because of the complexity of the
composition of ambient PM2.5 and
PM10–2.5, sources are best discussed in
terms of individual constituents of both
primary and secondary PM2.5 and
PM10–2.5. Each of these constituents can
have anthropogenic and natural sources.
Major components of fine particles are
sulfates, strong acid, ammonium nitrate,
organic compounds, trace elements
(including metals), elemental carbon,
and water. Primary and secondary fine
particles have long lifetimes in the
atmosphere (days to weeks) and travel
long distances (hundreds to thousands
of kilometers). They tend to be
uniformly distributed over urban areas
and larger regions, especially in the
eastern United States. As a result, they
are not easily traced back to their
individual sources. By contrast, coarse
particles are not readily transported
across urban or broader areas. These
particles can settle rapidly from the
atmosphere with lifetimes ranging from
minutes to days depending on their
specific size, atmospheric conditions,
and altitude.
(1) Health Effects
The EPA reported important progress
since the last PM NAAQS review in
advancing our understanding of
potential mechanisms by which ambient
PM2.5, alone and in combination with
other pollutants, is causally linked to a
number of key health effects. The more
extensive and stronger body of evidence
used by EPA to study the health effects
of PM2.5 in our latest review identified
a broader range of effects than those
previously documented, involving
premature mortality and indices of
morbidity (including respiratory
hospital admissions and emergency
room visits, school absences, work loss
days, restricted activity days, effects on
lung function and symptoms,
morphological changes, and altered host
defense mechanisms) associated with
both long- and short-term exposure to
PM2.5.
An overview of the scientific and
technical evidence considered in the
2004 CD and 2005 SP can be found in
our proposed rule for revising the
NAAQS for PM published at 70 FR
2619, January 17, 2006, beginning at
page 2626. The discussion which
follows is only a brief summary of those
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effects, with an explanation of the range
of PM2.5 concentrations that we
examined in considering revisions to
the primary PM2.5 NAAQS.
While most epidemiological studies
continue to be indexed by PM2.5, some
studies also implicate various
components within the mix of fine
particles that have been more commonly
studied (e.g., sulfates, nitrates, carbon,
organic compounds, and metals) as
being associated with adverse effects.
Furthermore, the available information
suggests that many different chemical
components of fine particles and a
variety of different types of source
categories are all associated with, and
probably contribute to, effects
associated with PM2.5. While there
remains uncertainty about the role and
relative toxicity of various components
of fine PM, the current evidence
continues to support the view that fine
particles should be addressed as a group
for purposes of public health protection.
Short-term exposure (from less than 1
day up to several days) to PM2.5 is likely
causally associated with mortality from
cardiopulmonary diseases, increased
hospitalization and emergency
department visits for cardiopulmonary
diseases, increased respiratory
symptoms, decreased lung function, and
changes in physiological indicators for
cardiovascular health. Effects associated
with short-term exposure identified
since the last NAAQS review include
increased non-hospital medical visits
(physician visits) and aggravation of
asthma associated with short-term
exposure to PM2.5. Although a growing
body of studies provided evidence of
effects associated with exposure periods
shorter than 24-hours (e.g., one to
several hours), EPA concluded in our
2004 SP that this information was too
limited to serve as a basis for
establishing a primary fine particle
standard with less than a 24-hour
averaging time. However, it was
concluded that this information added
weight to the importance of a 24-hour
standard. In addition, some studies
suggested consideration of a multipleday averaging time, but EPA concluded
that a multiple-day averaging time
would add complexity without
providing more effective protection than
a 24-hour averaging time.
For setting the level of the short-term
PM standard, EPA focused on a range of
24-hour 98th percentile PM2.5
concentrations of about 30 to 35 µg/m3.
Some new short-term mortality studies
considered for the last NAAQS review
provided evidence of statistically
significant associations with PM2.5 in
areas with air quality levels below the
level of the then-current primary 24-
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hour PM2.5 NAAQS (65 µg/m3). The
EPA observed a strong predominance of
studies with 24-hour 98th percentile
values down to about 39 µg/m3 showing
statistically significant association with
mortality, hospital admissions, and
respiratory symptoms. Within the range
of 24-hour average 98th percentile PM2.5
concentrations of about 30 to 35 µg/m3,
EPA no longer observed this strong
predominance of statistically significant
results. Below 35 µg/m3, EPA found
increasing variation in the short-term
exposure studies, which indicated an
increase in the uncertainty as to
whether likely causal associations could
be extended. In considering what level
would be appropriate for the primary
24-hour PM2.5 standard, the
Administrator indicated that in the
absence of evidence of any clear effects
thresholds, EPA had discretion to select
a specific standard level from within
this range of values. In ultimately
deciding to set the level of the primary
24-hour PM2.5 standard at 35 µg/m3, the
Administrator concluded that a
standard set at a higher level would not
likely result in improvement in air
quality in areas across the country in
which short-term exposure to PM2.5 can
reasonably be expected to be associated
with serious health effects. Similarly, a
standard set at a lower level was
rejected because of uncertainties in
interpreting the available epidemiologic
studies that could causally relate the
reported associations of health risks to
PM2.5 at those lower levels.
New epidemiologic studies have built
upon earlier limited evidence to provide
fairly strong evidence that long-term
exposure to PM2.5 is likely causally
associated with mortality from
cardiopulmonary disease, as well as
development of chronic respiratory
disease and reduced lung function
growth. The new studies also provide
evidence suggesting that long-term
exposure to fine particles is associated
with lung cancer mortality. The 2004
CD placed the greatest weight on reanalyses and extensions of two
mortality studies (Six Cities and
American Cancer Society (ACS) studies)
originally considered in the previous
NAAQS review. In the Six Cities study,
the long-term mean PM2.5 concentration
was 18 µg/m3, within an overall range
of 11 to 30 µg/m3. In the extended ACS
study, the mean for the more recent time
period used in the analysis was 14 µg/
m3, while the confidence intervals
around the relative risk functions start
to become appreciably wider (more
uncertain) below approximately 12 to 13
µg/m3. Based on this and other sets of
evidence, EPA decided to consider, for
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setting the level of the annual PM2.5
standard, a range of annual PM2.5
concentrations beginning somewhat
below 15 µg/m3 (the then-existing
primary annual PM2.5 NAAQS) down to
about 12 µg/m3. However, after carefully
considering public comments and
relevant studies, including the
uncertainties in interpreting the
available long-term exposure
epidemiologic studies, the
Administrator decided to retain the
level of the primary annual PM2.5
standard at 15 µg/m3 to protect public
health with an adequate margin of safety
from serious health effects. See 71 FR at
61177.
Despite the advances in knowledge
about the effects of PM2.5 on human
health, the 2005 SP noted the continued
difficulty of being able to establish a
dose-response relationship between
PM2.5 concentrations and specific
health-related effects. ‘‘The available
toxicologic studies have generally not
been designed to quantify dose-response
relationships* * *. Among the studies
reviewed [in the 2004 CD] are some that
report no evidence of a dose-response
relationship gradient, (CD, p. 7–152),
while some do (CD, p. 7–155), and the
CD draws no overall conclusions
regarding dose-response relationships
from toxicologic studies. Therefore,
while epidemiologic studies provide
clear indication of increasing response
with increasing concentration, no
conclusions can be drawn from
toxicologic evidence.’’ 2005 SP at 3–30.
(2) Welfare Effects
Ambient PM alone, and in
combination with other pollutants, can
have a variety of effects on public
welfare. While visibility impairment is
the most noticeable effect of fine
particles present in the atmosphere,
both fine and coarse particles can have
other significant welfare-related effects,
including effects on vegetation and
ecosystems, materials (e.g., soiling and
corrosion), and climate change
processes. In 1997, EPA established a
suite of secondary PM standards,
including annual and 24-hour PM2.5
standards and annual and 24-hour PM10
standards, to address visibility
impairment associated with fine
particles, and materials damage and
soiling related to both fine and coarse
particles. See 62 FR 38683. In 2006, EPA
considered the then-currently available
evidence and decided to revise the
current suite of PM2.5 secondary
standards by making them identical in
all respects to the revised suite of
primary PM2.5 standards, retain the
current 24-hour PM10 secondary
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standard, and revoke the current annual
PM10 secondary standard.
In reaching our decision in 2006 to
revise the suite of PM secondary
standards, EPA factored in several key
conclusions from the scientific and
technical information contained in the
2004 CD and 2005 SP. These
conclusions included the following: (1)
PM-related visibility impairment is
principally related to fine particle
levels, and most directly related to
instantaneous levels of visual air quality
associated with short-term averaging
periods; (2) PM2.5 concentrations can be
used as a general surrogate for visibility
impairment in urban areas; (3) any
secondary NAAQS for visibility
protection should be considered in
conjunction with the regional haze
program as a means of achieving
appropriate levels of protection against
PM-related visibility impairment in
urban, non-urban, and Class I areas
nationwide; (4) the available evidence is
not sufficient to support distinct
secondary standards for fine or coarse
particles for any non-visibility related
welfare effects; and (5) the secondary
standards should be considered in
conjunction with protection afforded by
other programs intended to address
various aspects of air pollution effects
on ecosystems and vegetation, such as
the acid deposition program and other
regional approaches to reducing
pollutants linked to nitrate or acidic
deposition.
Notwithstanding the conclusions
reached in setting the NAAQS for PM,
EPA has reviewed the scientific and
technical information concerning
welfare related effects considered in the
2004 CD and 2005 SP to determine
whether there is any basis for modifying
the safe harbor increments developed
for PM2.5 to satisfy the criteria under
sections 166(c) and 160 of the Act. The
EPA’s review began with visibility
impairment, followed by effects on
vegetation and other ecosystem
components, materials and soiling, and
climate changes.
(a) Visibility impairment.
The EPA has long recognized that
impairment of visibility is an important
effect of PM on public welfare. Visibility
can be defined as the degree to which
the atmosphere is transparent to visible
light. Visibility conditions are
determined by the scattering and
absorption of light by particles and
gases from both natural and
anthropogenic sources. The classes of
fine particles principally responsible for
visibility impairment are sulfates,
nitrates, organic matter, elemental
carbon, and soil dust.
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Visibility impairment can occur in
two principal ways: as local visibility
impairment (e.g., localized plumes) and
as regional haze. Local-scale impairment
is generally the result of the plume from
a single source or small group of local
sources, rather than from long-range
transport from more distant sources.
With this type of impairment, a band or
layer of discoloration can be observed
well above the terrain, obscuring the sky
or horizon relatively near the source, or
sources, which cause it. Such visibility
problems in urban areas are often
dominated by local sources, which may
include stationary, mobile and area
sources. Visibility impairment from the
combined effects of urban sources have
been studied in several major cities
because of concerns about fine particles
and their significant impacts on
residents of large metropolitan areas.
The second type of impairment,
regional haze, generally results from
pollutant emissions from a multitude of
sources located across a broad
geographic region. Regional haze can
impair visibility in every direction over
a relatively large area, in some cases
over multi-state regions. Regional haze
is principally responsible for
impairment in national parks and
wilderness areas (Class I areas) across
the country where scenic views are
considered an important attribute. Fine
particles transported from urban and
industrialized areas may, in some cases,
be significant contributors to regionalscale impairment in Class I and other
rural areas.
Annual average visibility conditions
vary regionally across the United States.
Higher visibility impairment tends to
occur more in the East, and is due to
generally higher concentrations of
anthropogenic fine particles and higher
relative humidity conditions. In
addition, the rural East generally has
higher levels of impairment than remote
sites in the West. For Class I areas,
visibility levels on the 20 percent
haziest days in the West are about equal
to levels on the 20 percent best days in
the East. For urban areas, however, East/
West visibility differences from fine
particles are substantially smaller than
they are in rural areas.
The EPA’s latest PM NAAQS review
focused on visibility impairment
primarily in urban areas for the
following reasons: (1) The efforts now
underway to address all human-caused
visibility impairment in Class I areas
through regional strategies under the
regional haze program (65 FR 35713,
July 1, 1999), and (2) new information
from visibility and fine particle
monitoring networks since the last PM
NAAQS review that has allowed for
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updated characterizations of visibility
trends and current levels in urban areas.
Given the strong link between visibility
impairment and short-term PM2.5
concentrations, EPA gave significant
consideration to the question of whether
visibility impairment in urban areas
allowed by the original 24-hour
secondary NAAQS for PM2.5 could be
considered adverse to public welfare.
New data available on PM2.5,
primarily in urban areas, enabled EPA
to better characterize urban visibility
than was previously possible. Such data
includes Federal Reference Method
(FRM) measurements of PM2.5 mass,
continuous measurements of hourly
PM2.5 mass, and PM2.5 chemical
speciation measurements. Using the
new data EPA sought to explore the
factors that historically complicated
efforts to address visibility impairment
nationally, including regional
differences related to levels of primarily
fine particles and relative humidity.
Using the most recent monitoring
information and analyses, as well as
photographic representations of
visibility impairment in several urban
areas to help inform judgments about
the acceptability of varying levels of
visual air quality in urban areas, EPA
observed that:
(1) At concentrations at or near the
level of the 24-hour PM2.5 standard (65
µg/m3), which equates to visual ranges
roughly around 10 kilometers (6 miles),
scenic views around and within the
urban areas, are significantly obscured
from view.
(2) Appreciable improvement in the
visual clarity of the scenic views occurs
at PM2.5 concentrations below 35 to 40
µg/m3, which equates to visual ranges
generally above 20 kilometers for the
urban areas considered.
(3) Visual air quality appears to be
good at PM2.5 concentrations generally
below 20 µg/m3, corresponding to visual
ranges of approximately 25 to 35
kilometers.
While being mindful of the
limitations in using visual
representations from a small number of
areas as a basis for considering national
visibility-based secondary standards,
EPA concluded that the observations
noted earlier supported consideration of
revising the then current PM2.5
secondary standards to enhance visual
air quality, particularly with a focus on
urban areas. This led to the evaluation
of information related to indicator,
averaging time, level, and form to
identify a range of alternative PM
standards that would protect visual air
quality, primarily in urban areas.
Notwithstanding the selection process
used in selecting the primary and
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secondary NAAQS for PM, for this PM
increment proposal we are examining
the same information to determine
whether it might justify modifying the
safe harbor increments for PM2.5, which
follow the indicator, averaging times,
and form of the NAAQS for PM2.5, as
described earlier as option 1.
PM indicator. While both fine and
coarse particles contribute to visibility
impairment, visibility impairment is the
most noticeable effect of fine particles
present in the atmosphere. Analyses of
hourly PM2.5 measurements and other
information demonstrate that fine
particles contribute to visibility
impairment directly in proportion to
their concentration in the ambient air.
Moreover, hygroscopic components of
fine particles, in particular sulfates and
nitrates, contribute disproportionately
to visibility impairment under high
humidity conditions, when such
components reach particle diameters up
to and even above 2.5 µm. The EPA’s
analyses of how well PM2.5
concentrations correlated with visibility
in urban locations across the United
States lead to the conclusion that the
observed correlations were strong
enough to support the use of PM2.5 as
the indicator for standards to address
visibility impairment in urban areas,
especially when the indicator is defined
for a relatively short period of daylight
hours.
Averaging time. While EPA selected
the 24-hour averaging time for the PM2.5
secondary standard to address visibility
impairment primarily in urban areas, a
range of shorter term (sub-daily)
daylight averaging times were also
considered. Strong correlations between
visibility and PM2.5 concentrations were
found to occur at the 24-hour averaging
time, but the strongest correlations were
found to occur at the sub-daily daylight
averaging times, e.g., 4-to 8-hour
daylight averaging times. In fact, the
correlation was greatest in the 4-hour
time period between 12 and 4 p.m. At
the sub-daily daylight averaging times,
correlations between PM2.5
concentrations and light extinction were
less influenced by relative humidity and
more consistent across regions.
A number of different daylight time
periods was selected to compare
correlations between visibility and
hourly PM2.5 concentrations in urban
areas across the United States and in
eastern and western regions. Ultimately,
EPA staff recommended consideration
of a short-term averaging time, within
the range of 4 to 8 hours, within a
daylight time period between
approximately 10 a.m. to 6 p.m., to
target the driest part of the day. Most
CASAC Panel members supported the
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SP recommendation of a sub-daily
averaging time.
Following careful consideration of the
various sets of data and evidence
concerning visibility impairment, the
Administrator proposed to revise the
secondary 24-hour standard for PM2.5 to
make it identical to the proposed
revised primary PM2.5 standard (based
on a 24-hour averaging time for the
short-term standard). Consistent with
recommendations to consider a subdaily averaging time, the Administrator
also solicited comment on 4-to 8-hour
averaging time for the secondary PM2.5
standard. In reaching his final decision
to rely on the 24-hour averaging period
to set the secondary standard for PM2.5,
the Administrator concluded that the
relative protection against adverse
effects on public welfare provided by
the proposed primary standards was
equivalent or more protective than
several of the 4-hour secondary standard
alternatives in the range recommended
by CASAC and the SP. He also believed
that caution was warranted in
establishing a distinct secondary
standard for visibility impairment
primarily in urban areas, given the
limitations in the underlying studies
and the subjective nature of the
judgment required.
Level of increment. In evaluating the
adequacy of the levels of the contingent
safe harbor increments for PM2.5, we
examined the range of PM2.5
concentrations considered in setting a
national visibility standard primarily for
urban areas. We had established that
range of concentrations by using the
results of public perception and attitude
surveys conducted in the United States
and Canada, State and local visibility
standards within the United States, and
visual inspection of photographic
representations of several urban areas
across the United States. These
approaches are detailed in the 2005 SP
(pp. 6–18 to 6–23.)
The public perception and attitude
studies were used to gain an
understanding of what the public
regarded as an acceptable visible range.
In some urban areas, poor visibility has
led to more localized efforts to better
characterize, as well as improve, urban
visibility conditions. Public perception
surveys used in Denver, Phoenix, and
British Columbia studies yielded
reasonably consistent results, with each
study indicating that a majority of
citizens find value in protecting local
visibility to with a visual range of about
40 to 60 km. Visibility standards for the
Lake Tahoe area in California and for
areas within the State of Vermont are
both targeted at a visual range of about
50 km. In contrast, California’s
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longstanding general state-wide
visibility standard is a visual range of
approximately 16 km.
Aided by photographic
representations of varying levels of
visual air quality developed for several
cities across the United States, EPA staff
reached the conclusion that a national
visibility standard in the PM2.5
concentration range of 30 to 20 µg/m3
should be considered. Further analyses
to characterize the distributions of PM2.5
concentrations, 4-hour averages in the
12 to 4 p.m. time frame, by region, that
correspond to various visual range target
levels, resulted in a finding that
concentrations of 30, 25, and 20 µg/m3
correspond to the target visual ranges of
approximately 25, 30 and 35 km,
respectively. Thus, it was determined
that a standard set within the range of
30 to 20 µg/m3 could be expected to
correspond generally to media visual
range levels of approximately 25 to 35
km in urban areas across the United
States. This range was generally
consistent with a national target visual
range below 40 km, the level suggested
by the public perception surveys and
the local visibility standards and goals.
Nevertheless, EPA staff noted that a
standard set at any specific
PM2.5concentration will necessarily
result in visual ranges that vary
somewhat in urban areas across the
country, reflecting in part the less-thanperfect correlation between PM2.5
concentrations and reconstructed light
extinction. 2005 SP at page 7–8.
Form of increment. In considering a
reasonable range of forms for a PM2.5
standard within the range of PM2.5
concentration levels being considered,
EPA staff took into account the same
general factors that were taken into
account in considering an appropriate
form for the primary PM2.5 standard. In
that case, EPA staff concluded that a
concentration-based form should be
considered because of its advantages
over the previously used expectedexceedance form.14 For visibility, the
advantages are that the concentrationbased form (1) Would give
proportionally greater weight to days
when the PM-related visibility
impairment is substantially higher than
to days just above the standard, and (2)
has greater stability. 2005 SP at 7–11. To
identify a range of concentration
percentiles that would be appropriate
for consideration, it was concluded that
14 The form of the 1987 24-hour PM
10 standard is
based on the expected number of day per year
(averaged over 3 years) on which the level of the
standard is exceeded; thus, attainment with the
one-expected exceedance form is determined by
comparing the fourth-highest concentration in 3
years with the level of the standard.
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the upper end of the range of
consideration should be the 98th to 99th
percentile, consistent with the forms
being considered for the 24-hour
primary PM2.5 standard. For the lower
end of the range, EPA staff used the
92nd percentile because it represented
the mean of the distribution of the 20
percent worst days, consistent with the
fact that the regional haze program
targets the 20 percent most impaired
days for improvements in visual air
quality in Class I areas. 2005 SP at 7–
12.
While EPA staff regarded PM2.5 as the
best indicator for addressing visibility
impairment in urban areas, they
considered a range of averaging times,
levels, and forms for setting a PM2.5
secondary standard. In summary, EPA
staff recommended that consideration
be given to a short-term averaging time
for a PM2.5 standard, within the range of
4 to 8 hours, within a daylight time
period between approximately 10 a.m.
to 6 p.m. In addition, they
recommended that consideration should
be given to the adoption of Federal
equivalent methods for appropriate
continuous methods for measurement of
short-term average PM2.5 concentrations
to facilitate implementation of the
standard. Within the recommended 4- to
8-hour averaging time, the EPA staff
recommended consideration of a
standard level within the range of 30 to
20 µg/m3, depending in part on the form
of the standard selected. Finally, staff
recommended consideration of a
percentile-based form, focusing on a
range from the 92nd percentile up to the
98th percentile of the annual
distribution of daily short-term PM2.5
concentrations averaged over 3 years.
2005 SP at 7–13.
(b) Vegetation and other ecosystem
components.
The 2004 CD found that then-current
PM2.5 levels in the United States ‘‘[had]
the potential to alter ecosystem
structure and function in ways that may
reduce their ability to meet societal
needs’’ (CD, p. 4–153). However, studies
show that vegetation and other
ecosystem components result
predominantly from exposure to excess
amounts of specific chemical species
than from particle source, predominant
form (particle, gas, or liquid) or size
fraction. The 2004 CD discussed the
effects of a number of different chemical
species, including dust, trace metals,
and organics, found within ambient PM,
but ultimately focused on particulate
nitrates and sulfates based on the
conclusion that these latter constituents
of PM2.5 were ‘‘of greatest and most
widespread environmental
significance.’’ Thus, the 2005 SP
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focused on the welfare effects of
particulate nitrates and sulfates, either
individually, in combination, and/or as
contributors to total reactive nitrogen
deposition and total deposition of
acidifying compounds on sensitive
ecosystem components and essential
ecological attributes.
Nitrogen and sulfur in varying
amounts are necessary and beneficial
nutrients for most organisms that make
up ecosystems. It is when unintentional
additions of atmospherically derived
nutrient and acidifying compounds
containing nitrogen and sulfur force
unintended change on ecosystems,
resulting in adverse impacts on essential
ecological attributes, that deposited
particulate nitrate and sulfate are
termed ecosystem ‘‘stressors.’’ In order
for any specific chemical stressor
present in ambient PM to impact
ecosystems, it must first be removed
from the atmosphere through any of
three different types of deposition: wet
(rain/frozen precipitation), dry, or
occult (fog, mist, or cloud). At the
national scale, all types of deposition
must be considered in determining
potential impacts to vegetation and
ecosystems because each type may
dominate over specific intervals of time
or space.
The most significant PM-related
ecosystem-level effects result from longterm cumulative deposition of a given
chemical species (e.g., nitrate) or mix
(e.g., acidic or acidifying deposition)
that exceeds the natural buffering or
storage capacity of the ecosystem and/
or affects the nutrient status of the
ecosystem. The 2005 SP examined the
environmental effects of both reactive
nitrogen (of concern is the reactive
nitrogen resulting from the conversion
of both atmospheric nitrogen and fossil
nitrogen during the combustion of fossil
fuels) and PM-related acidic and
acidifying deposition on various
ecosystems, including vegetation,
terrestrial ecosystems, threatened and
endangered species, and aquatic habitat.
Vegetation. Various studies indicate
that at current ambient levels, risks to
vegetation from short-term exposures to
dry deposited particulate nitrate or
sulfate are low; however, when found in
acidifying deposition, such particles do
have the potential to cause direct foliar
injury. The 2005 SP concluded on the
basis of available information that the
risk of injury occurring from acid
precipitation in the eastern United
States is high, noting that acid
precipitation with levels of acidity
associated with adverse foliar effects
exist in some locations of the United
States. Such adverse effects may include
damage to leaf surface structure;
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increased permeability of leaf surface to
toxic material, water, and disease
agents; increased leaching of nutrients
from foliage; altered reproductive
processes; and overall weakening of
trees making them more susceptible to
other stressors. Having said all this, the
2005 SP also found that the contribution
of particulate sulfates and nitrates to the
total acidity found in the acid
precipitation impacting eastern
vegetation is not clear.
Terrestrial ecosystems. The 2005 SP
concluded that excess nitrogen
deposition is having a ‘‘profound and
adverse impact on the essential
ecological attributes associated with
terrestrial ecosystems.’’ Terrestrial
ecosystems may be adversely impacted
by (1) increased nitrogen associated
with atmospheric deposition, surface
runoff, or leaching from nitrogen
saturated soils into ground or surface
waters; and (2) acidic and acidifying
deposition.
Long-term, chronic additions of
reactive nitrogen (including nitrate
deposition and ammonium from
ambient PM) can cause the nitrogen
input to plants to exceed the natural
capacity of plants and soil
microorganisms to utilize and retain the
nitrogen needed for normal growth. As
this excess occurs over time, a
detrimental ecological condition known
as ‘‘nitrogen saturation’’ is said to exist.
Nitrogen saturation does not occur at
a specific point in time, but reflects a set
of gradually developing critical changes
in the ecosystem process. In addition,
not all vegetation, organisms, or
ecosystems react in the same manner to
increased nitrogen availability from
nitrogen deposition. Those plants that
are predisposed to capitalize on any
increases in nitrogen availability gain an
advantage over those that are not as
responsive to added nitrogen. Over
time, this shift in the competitive
advantage may lead to shifts in overall
plant community composition. Whether
this shift is considered adverse would
depend on the management context
within which that ecosystem falls and
the ripple effects of this shift on other
ecosystem components, essential
ecosystem attributes, and ecosystems.
The addition of nitrogen on plant
community succession patterns and
biodiversity has been studied in several
long-term nitrogen fertilization studies
in both the United States and Europe.
These studies suggest that some forests
receiving chronic inputs of nitrogen
may decline in productivity and
experience greater mortality. Some of
the U.S. forests that are showing severe
symptoms of nitrogen saturation are: the
northern hardwoods and mixed conifer
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forests in the Adirondack and Catskill
Mountains of New York; the red spruce
forests at Whitetop Mountain, Virginia,
and Great Smoky Mountains National
Park, North Carolina; mixed hardwood
watersheds at Fernow Experimental
Forest in West Virginia; American beech
forests in Great Smoky Mountains
National Park, Tennessee; and mixed
conifer forests and chaparral watersheds
in southern California and the
southwestern Sierra Nevada in Central
California. 2005 SP at 6–31.
Studies have shown that acid
deposition has changed the chemical
composition of soils by depleting the
content of available plant nutrient
cations (e.g., Ca2+, Mg2+, and K+) by
increasing the mobility of aluminum,
and by increasing the sulfur and
nitrogen content. Effects of acidic
deposition have been extensively
documented, as discussed in the 2004
CD and reports referenced therein. For
example, effects on some species of
forest trees linked to acidic deposition
include increased permeability of leaf
surfaces to toxic materials, water, and
disease agents; increased leaching of
nutrients from foliage; and altered
reproductive processes; all of which
serve to weaken trees so that they are
more susceptible to other stresses (e.g.,
extreme weather, pests, and pathogens).
In particular, acidic deposition has been
implicated as a causal factor in the
northeastern high-elevation decline of
red spruce. Although U.S. forest
ecosystems other than the highelevation spruce-fir forests are not
currently manifesting symptoms of
injury directly attributable to acid
deposition, less sensitive forests
throughout the United States are
experiencing gradual losses of base
cation nutrients, which in many cases
will reduce the quality of forest
nutrition over the long term.
Threatened and endangered species.
The adverse ecological effects of PM
include those effects on rare and unique
ecosystems, including both plant and
wildlife species. Nitrogen deposition,
including particulate nitrate, may have
a direct adverse affect on some plant
species, while for others the harm
results when added nitrogen serves as a
nutrient for some invasive species that
eventually replace the more sensitive,
rare species.
In some instances, as sensitive
vegetation is harmed or lost, wildlife
species that depend on these plants are
also adversely affected. Several
threatened or endangered species listed
by the U.S. Fish and Wildlife Service,
such as the desert tortoise and
checkerspot butterfly have declined as a
result of native food supplies being
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replaced by invasive plant species
whose productivity is enhanced in part
by nitrogen deposition.
Aquatic habitat. Adverse effects of
PM on aquatic systems (streams, rivers,
lakes, estuaries, and oceans) can be the
result of either elevated levels of
reactive nitrogen input or acidification.
In either case, the nitrogen input
contribution from PM may be the result
of atmospheric deposition directly into
the water body or on terrestrial
ecosystems, reaching the water body via
surface runoff or leaching from nitrogen
saturated soils into ground or surface
waters. However, it is not clear how
much of the total nitrogen input to
aquatic systems results from
atmospheric deposition rather than from
other nitrogen sources.
Estuaries receive far greater nutrient
inputs than other systems. Excess
nitrogen in estuaries results in eutrophic
conditions whereupon dissolved oxygen
is significantly reduced; yielding an
environment that favors plant life over
animal life. The 2005 SP describes
research being done in the Pamlico
Sound in North Carolina, which is a key
fisheries nursery in the southeastern
United States. Studies have shown that
direct nitrogen deposition onto
waterways feeding into the Pamlico
Sound or onto the Sound itself and
indirect nitrogen inputs via runoff from
the upstream watersheds contribute to
conditions of severe water oxygen
depletion; formation of algae blooms in
portions of the Pamlico Sound estuarine
complex; altered fish distributions,
catches, and physiological states; and
increases in the incidence of disease.
2005 SP at p. 6–35.
Other studies have shown that under
extreme rainfall events, massive
influxes of reactive nitrogen (in
combination with excess loadings of
metals or other nutrients) into
watersheds and sounds can lead to
dramatic decreases of oxygen in water
and the creation of widespread ‘‘dead
zones’’ and/or increases of algae blooms
that can cause extensive fish kills and
damage to commercial fish and sea food
harvesting. 2005 SP at p. 6–35.
The 2005 SP indicates that there is a
clear link between acidic water, which
results from atmospheric deposition of
strong acids, and fish mortality. Studies
have shown that inputs of acid
deposition to regions with base-poor
soils have resulted in the acidification
of soil waters, shallow ground waters,
streams, and lakes in a number of
locations with the United States. This
can result in lower pH and higher
concentrations of inorganic monomeric
aluminum, which causes changes in
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chemical conditions that are toxic to
fish and other aquatic animals.
(c) Materials damage and soiling.
As part of the review for setting
secondary standards for PM, the 2004
CD and 2005 SP considered the adverse
effects that the deposition of ambient
PM can have on materials such as
metals, paint finishes, and building
stone and concrete. Substantial
evidence exists to show that ambient
PM plays a role in both physical damage
and impaired aesthetic qualities of
materials. Physical damage to materials,
including corrosion, degradation, and
deterioration, is known to result from
exposure to environmental factors such
as sunlight, moisture, fungi, and varying
temperatures; however, to the extent
that particles may cause or contribute to
physical damage of building materials,
such damage is primarily caused by
chemically active—especially
particulate nitrates and sulfates—fine
particles or hygroscopic coarse particles.
On the other hand, particles consisting
of carbonaceous compounds are
responsible for soiling of commonly
used building materials and culturally
important items (statues, works of art,
etc.) Soiling or exposure to PM can
affect the aesthetic appeal of surfaces by
giving them a dirty appearance,
resulting in an increased frequency of
cleaning. Nevertheless, while the role of
ambient PM in specific adverse effects
is well documented in the available
studies, the 2004 CD and 2005 SP also
concluded that there remains
insufficient evidence to establish a
quantitative relationship between
ambient PM and any of the various
effects described.
The EPA believes that these
observations and the underlying
available evidence continue to support
consideration of retaining an
appropriate degree of control on both
fine and coarse particles. Lacking any
specific quantitative basis for
establishing distinct standards to protect
against PM related to adverse effects on
materials, EPA believes that reductions
in fine and coarse particles likely to
result from the current suite of
secondary PM standards, or the range of
recommended revisions to the primary
PM standards and to the secondary
PM2.5 standard to address visibility
impairment, would contribute to
protection against PM-related soiling
and materials damage.
(d) Climate and solar radiation
effects.
The effects of PM on climate result
from either the scattering or absorption
of radiation by ambient particles,
resulting in a cooling or warming effect
on climate, respectively. Studies suggest
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that global and regional climate changes
could have both positive and negative
effects on human health and welfare,
and the environment. Most components
of ambient PM, especially sulfates,
scatter and reflect incoming solar
radiation back into space. However,
some components of ambient PM,
especially black carbon, absorb
incoming solar radiation or outgoing
terrestrial radiation. Sulfate particles
indirectly affect climate by serving as
condensation nuclei which alter the size
distribution of cloud droplets
(producing more droplets with smaller
sizes), causing the amount of solar
radiation that clouds reflect back to
space to increase.
While substantial qualitative
information has shown the important
role that ambient PM plays in both
global and regional climatic processes,
that role is presently poorly quantified.
There are considerable uncertainties
and difficulties in projecting likely
climate change impacts. The 2005 SP
indicates that ‘‘any complete assessment
of the direct radiative effects of PM
would require computationally
intensive calculations that incorporate
the spatial and temporal behavior of
particles of varying composition that
have been emitted from, or formed by
precursors emitted from, different
sources.’’ 2005 SP at 6–55. In addition,
calculations of indirect physical effects
of particles on climate are subject to
much larger uncertainties than those
related to the direct radiative effects of
particles.
Exposure to solar radiation may have
direct effects on human health and
agricultural and ecological systems;
indirect effects on human health and
ecosystems, and effects on materials.
2005 SP at 6–56ff. Several studies cited
in the 2004 CD reinforce the idea that
particles can play an important role in
affecting the transmission of solar UV–
B radiation. However, none of these
studies included measurements of
ambient PM concentrations, so that
direct relationships between PM levels
and UV–B radiation transmission could
not be determined. In addition, the
relationships between particles and UV–
B radiation transmission can vary
considerably over location, conditions,
and time. 2005 SP at 6–56. In summary,
the EPA staff concluded that available
information is insufficient to project the
extent to which, or even whether,
location-specific changes in ambient PM
would indirectly affect human health or
the environment.
e. Fundamental Elements of Increments
As we have previously noted, under
the model established in the Act and
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prior EPA regulations, the function of an
increment is not like that of the NAAQS
in that an increment is not intended to
set a uniform ambient pollutant
concentration ‘‘ceiling’’ across the
United States. See 70 FR 59600. That is,
while both increments and NAAQS
generally serve to limit air pollution
levels, increments are designed to allow
a uniform degree of pollutant
concentration increase for each area in
the United States with a particular
classification, with the allowable
increase measured against a baseline air
quality level for a particular area.15
Because the baseline air quality level
varies from one location to another, and
is not established until a PSD permit is
submitted, it is not possible to
determine what the maximum pollutant
concentration attainable is for a given
area (to be used to determine the
protection afforded by an increment
against potential adverse environmental
effects) until the specific baseline air
quality level is known.
For the reasons described in our
increments rule for NOX, our objective
is to establish uniform increments that
allow the same level of deterioration for
each area of the country having the
same classification. 70 FR 59601. Our
goal is not to establish increments to
reduce existing air pollutant
concentrations below baseline levels in
each area, but rather to define a level of
increase in pollutant concentrations
above baseline levels that represents
‘‘significant’’ deterioration for each area
classification. 70 FR 59600.
f. Evaluation of the Safe Harbor
Increments
Mindful of the considerations we
previously described about the
fundamental characteristics of the
increments, we reviewed the scientific
and technical evidence available for the
2005 review of the NAAQS for PM in
order to determine whether, and to what
extent, the ‘‘safe harbor’’ increments
might need to be modified in order to
protect air quality values, health and
welfare, and parks while ensuring
economic growth consistent with the
preservation of clean air resources in
accordance with sections 166(c) and 160
of the Act. As we did in our evaluation
of the safe harbor NO2 increments, we
propose to rely on an approach that
evaluates how protective the safe harbor
PM2.5 increments are by trying to
compare the marginal pollutant
concentration increases allowed by the
15 It should be noted, however, that an increment
does not allow air pollution levels in an area to
increase beyond the ambient concentration of a
pollutant that would exceed the level allowed by
the NAAQS.
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safe harbor increment levels against the
pollutant concentrations at which
various environmental responses occur.
We analyzed the available evidence
from both a quantitative and qualitative
perspective to reach a decision about
whether we should modify the
contingent safe harbor PM2.5 increments
and whether we have sufficient
information to select a specific
alternative level, averaging time, or
pollutant indicator for the increments.
(1) Non-Visibility Related Effects
In quantitatively evaluating the
adequacy of the contingent safe harbor
increments for PM2.5 for non-visibility
related welfare effects, we experienced
difficulties with identifying the
appropriate indicator, as well as to the
level of the increments. In the most
recent evaluation of the NAAQS for PM,
EPA staff concluded that ‘‘sufficient
information is not available at this time
to recommend consideration of either an
ecologically based indicator or an
indicator based distinctly on soiling and
materials damage, in terms of specific
chemical components of PM.’’ 2005 SP
at 7–15. For consideration of the effects
of ambient PM on vegetation and other
ecosystems, the available data indicate
that the chemical species of PM
(especially particulate nitrate and
sulfate) has more relevance than the size
fraction (coarse or fine). Acid
precipitation, including particulate
sulfate, has been found to be
particularly damaging to foliage, and
along with ambient SO2 contributes
significantly to materials damage and
soiling.
Determining the most effective levels
for any indicator for PM from the
available data is difficult because the
evidence is insufficient to provide a
quantitative relationship between
ambient PM concentrations and known
and observed adverse ecological effects.
Fundamental areas of uncertainty
preclude establishing predictable
relationships between ambient
concentrations of particulate nitrogen
and sulfur compounds and associated
ecosystem effects. One source of
uncertainty hampering the
characterization of such relationships is
the extreme complexity and variability
that exist in estimating particle
deposition rates. These rates are affected
by numerous factors, including particle
size and composition, associated
atmospheric conditions, and the
properties of the surfaces being
impacted. A related source of
uncertainty is establishing the portion of
the total nitrogen and sulfur deposition
occurring at a given site is attributable
to ambient PM. Though several national
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deposition monitoring networks have
been successfully measuring wet and
dry deposition for several decades, they
often do not distinguish the form (e.g.,
particle, wet, and dry gaseous) in which
a given chemical species is deposited.
Further, it is not clear how well data
from monitoring sites may apply to nonmonitored sites with different surface
cover, meteorology, or other deposition
related factors.
Another fundamental problem that
makes it difficult to establish a
meaningful dose-response relationship
between ambient PM levels and specific
adverse environmental effects is that
ecosystems have different sensitivities
and capacities to buffer or assimilate
pollutants. Many of the documented
ecosystem-level effects only became
evident after long-term, chronic
exposures to total annual loads of
reactive nitrogen (Nr) or acidifying
compounds that eventually exceeded
the natural buffering or assimilative
capacity of the system. In most cases,
PM deposition is not the only
contributor to the total load of Nr or
acidifying compounds entering the
affected system. Since it is difficult to
predict the rate of PM deposition, and
thus, the PM contribution to total
deposition at a given site, it is difficult
to predict the ambient concentration of
PM that would likely lead to the
observed adverse effects within any
particular ecosystem. Equally difficult is
the prediction of recovery rates for areas
already affected, if PM deposition rates
of various chemical species were to be
reduced.
In response to our 2005 proposal for
NO2 increments, some commenters
expressed the opinion that a better way
of identifying acceptable pollutant
loadings, particularly for protection
against ecological effects, is the use of
a ‘‘critical load’’ concept.16 70 FR
59612. At that time, EPA expressed
support for the concept, but indicated
that our current knowledge about
critical loads did not ‘‘provide a
sufficient basis for establishing a
uniform, national standard such as a
PSD increment.’’
The critical load concept was once
again reviewed in the 2005 SP for PM.
It was noted in that document that the
‘‘[k]ey to the establishment of a critical
load is the selection of appropriate
ecological endpoints or indicators that
are measurable characteristics related to
16 A ‘‘critical load’’ is a numerical estimate of the
amount of polloution that a sensitive ecosystem can
absorb on a sustained basis before it experiences a
measurable amount of degradation. In contrast to
the units for increments, µ/m3, a critical load is
typicallly expressed as a loading rate in kilograms
of a pollutant per hectare per year.
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the structure, composition, or
functioning of ecological systems (i.e.,
indicators of condition).’’ 2005 SP at 6–
46. The EPA recognized the value of
using critical loads and acknowledged
that a number of different groups in the
United States have begun to use or
develop critical loads. Nevertheless,
while recognizing that current activities
‘‘hold promise,’’ EPA concluded that
‘‘widespread use of [critical loads] in
the U.S. is not yet possible.’’ Among
other things, currently available data are
insufficient to quantify the contribution
of ambient PM to total Nr or acid
deposition, and it is not clear whether
a critical load could be developed just
for the portion of the total N or S input
that is contributed by PM. SP at 4–49.
Research, in conjunction with the
development of improved predictive
models, could help in future
consideration within the United States
of the critical loads concept, and in
determining how much of any given
critical load is contributed by different
sources of pollutants.
As explained earlier, the available
scientific and technical data do not yet
enable us to adequately relate ambient
concentrations of PM2.5 to ecosystem
responses. Without such key
information, it is difficult to
quantitatively evaluate the effectiveness
of the ‘‘safe harbor’’ increments for
protecting air quality values, health and
welfare, and parks while ensuring
economic growth consistent with the
preservation of clean air resources.
Alternatively, we must make a
qualitative judgment as to whether the
contingent safe harbor increments for
PM2.5 or some alternative increments
meet the applicable factors.
In this situation, we believe that the
determination of the increment levels
that satisfy the factors applicable under
section 166(c) is ultimately a policy
choice that the Administrator must
make, similar to the policy choice the
Administrator must make in setting a
primary NAAQS ‘‘with an adequate
margin of safety.’’ See Lead Industries
Ass’n v. EPA, 647 F.2d 1130, 1147 (D.C.
Cir. 1980) (where information is
insufficient to permit fully informed
factual determinations, the
Administrator’s decisions rest largely on
policy judgments). Using a similar
approach is warranted because both
section 109 and section 160(1) direct the
Administrator to use his or her
judgment in making choices regarding
an adequate margin of safety or
protecting against effects that may still
occur notwithstanding compliance with
the NAAQS—both areas of inquiry
characterized by great uncertainty.
Thus, in the process for setting NAAQS,
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the Administrator looks to factors such
as the uncertainty of the science, the
seriousness of the health effects, and the
magnitude of the environmental
problem (isolated or commonplace).
E.g., 62 FR 38652 (July 18, 1997) (PM2.5
NAAQS).
Bearing on this policy decision for
increments are various considerations,
based on the available information and
the factors applicable under section
166(c). The factors establishing
particular environmental objectives
(protecting air quality values, health and
welfare, and parks) might suggest that,
in some areas, we permit little or no
increase in PM2.5 emissions or establish
an increment for another form of PM
because there are data indicating that an
effect may be attributable to PM
emissions. However, as explained in the
NOX rule, we do not believe that
Congress intended for the PSD program
to eliminate all negative effects. Thus,
rather than just seeking to eliminate all
negative effects, we must attempt to
identify a level of increase at which any
additional effects beyond existing (or
baseline) levels would be ‘‘significant’’
and protect against those ‘‘adverse’’
effects. Furthermore, we need to ensure
that our increments provide room for
some economic growth. Congress
intended for EPA to weigh these
considerations carefully and establish
regulations that balance economic
growth and environmental protection.
Since we are unable to establish a
direct, widely applicable, quantitative
relationship between particular levels of
PM2.5 and specific negative effects, we
give particular weight to the policy
judgment that Congress made when it
set the statutory increments as a
percentage of the NAAQS and created
increments for the same pollutant form
and time period that was reflected in the
NAAQS. In section 166 of the Act,
Congress directed that EPA study the
establishment of PSD regulations for
other pollutants for which Congress did
not wish to set increments at the time.
Congress’s own reluctance to set
increments to prevent significant
deterioration of air quality due to
emissions of NOX, and the provisions
ensuring time for Congressional review
and action, suggest that Congress
intended for EPA to avoid speculative
judgments about the science where data
are lacking. Thus, in the absence of
specific data showing that an increment
level that of the ‘‘safe harbor’’ level
would better protect health, welfare,
parks, and air quality values, while
simultaneously maximizing
opportunities for economic growth, we
give weight in our qualitative analysis of
the factors applicable under section
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166(c) to the method that Congress used
to establish the statutory increments.
In making this qualitative judgment,
we also consider the overall regulatory
framework that we have established in
the PSD regulations for PM2.5. This
framework includes a case-by-case
analysis of each permit application to
identify additional impacts (e.g., soils
and vegetation), a special review by the
FLM and State reviewing authority of
potential adverse effects on air quality
values in parks and special areas, and a
requirement that all new and modified
sources install BACT. In addition, the
area classification system ensures that
there will be economic growth in
particular areas that is consistent with
the values of each State and its
individual communities. Based on this
qualitative analysis, we do not believe it
is necessary to adopt more stringent
increments to satisfy section 166(c) of
the Act with respect to non-visibility
related effects.
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(2) Visibility Protection
In the case of visibility protection, the
available evidence was strong enough to
enable EPA to conclude that PM2.5 is the
appropriate indicator for measuring the
effects of ambient PM on visibility
impairment. Accordingly, using PM2.5
concentrations as the basis for review,
EPA evaluated a range of PM2.5 ambient
concentrations, averaging times (24
hours and less), and a range of
concentration percentiles (using a
concentration-based form for the
standard) in order to establish a
recommendation for setting the
secondary NAAQS for PM to address
visibility impairment in urban areas. As
explained in the 2005 SP, EPA
considered, as a lower bound for setting
the short-term secondary PM2.5
standard, a PM2.5 concentration of either
20 or 25 µg/m3, averaged over a 4- to 8hour averaging time within daylight
hours, depending on the percentile
range considered for the form of the
standard.
The Class II, short-term safe harbor
increment for PM2.5 is 9 µg/m3. This
level is well below the lower bound
recommended for setting the secondary
PM2.5 standard, but is based on a 24hour averaging time at the 98th
percentile. The 2005 SP also notes that
the estimated 98th percentile values in
distributions of daily background levels
are below 10 µg/m3 in most areas. Thus,
the allowable deterioration from the safe
harbor increment in addition to the
natural background level generally falls
below the minimum values
recommended in the 2005 SP for the
secondary short-term standard for PM2.5.
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With regard to the Class I increments
for PM2.5, we note that Congress
explicitly included visibility as an air
quality related value (AQRV), enabling
Federal land managers to protect
significant attributes of Federal Class I
areas. Act section 165(d)(2)(B). The
FLM, assigned the affirmative
responsibility to protect Federal Class I
areas, are to use AQRVs which are
separate and distinct from increments,
to address individual Class I areas and
the unique attributes identified for each
Class I area. Congress recognized that
AQRVs and increments were not the
same thing and established independent
procedures for the implementation of
each. For example, the Act authorizes
FLM to evaluate the effects of pollutant
increases using AQRVs as the basis
regardless of the effect of such pollutant
increases on the increments. In using
the AQRV, FLM are not limited in their
evaluation by the maximum allowable
pollutant increase set by the increment
and may identify adverse impacts on
visibility pursuant to AQRVs even when
the pollution increase will not cause or
contribute to an exceedance of an
increment. Instead, the pollutant
increase is evaluated against the AQRV
which considers the specific conditions
existing in the Class I area of concern.
Thus, regardless of the increased
amount of pollution that an increment
may allow, the FLM may determine that
the visibility in the Class I area is
adversely affected by an amount of
pollutant increase less than that allowed
by the increment.
From a qualitative perspective, we
believe that visibility protection in Class
I areas is more adequately provided by
the AQRV process, where each area can
be addressed on the basis of the local
situation and the FLM’s assessment of
potential ambient impacts by a
particular source. Nevertheless,
generally speaking an increment should
not be so large that it routinely results
in substantially more pollution in Class
I areas than is generally acceptable
under the AQRV approach. The
contingent safe harbor PM2.5 increments
for Class I areas are 1 µg/m3 and 2 µg/
m3 for the annual and 24-hour averaging
periods, respectively.
We believe the importance of using
distinct PM2.5 increments to protect
against visibility impairment is also
lessened by the fact that Congress,
aware of the statutory requirements for
prevention of significant deterioration of
air quality, established several visibility
programs that specifically target
emissions reductions to achieve the
desired visibility benefits. Under the
regional haze regulations, promulgated
by EPA in 1999, States are required to
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establish goals for improving visibility
on the 20 percent most impaired days in
each Class I area, and for allowing no
degradation on the 20 percent least
impaired days. Each State must adopt
emission reduction strategies which, in
combination with the strategies of
contributing States, assure that Class I
area visibility improvement goals are
met. Five multi-state planning
organizations are evaluating the sources
of PM2.5 contributing to Class I area
visibility impairment to lay the
technical foundation for developing
strategies, coordinated among many
States, in order to make reasonable
progress in Class I areas across the
United States.
We believe it is also important to
consider the fact that some State and
local governments have also developed
programs to improve visual air quality
in specific urban areas. These programs
are individually designed to focus on
improving visibility to a visual range
defined by the specific area of concern.
Such local programs can more
appropriately focus on the preferences
of individual communities where a
uniform national increment for visibility
protection generally cannot.
In setting the NAAQS for PM, EPA
ultimately concluded that a distinct
secondary standard with a different
averaging time or form was not
warranted at that time. Instead, we
concluded that a set of secondary PM2.5
standards set identical to the revised
primary PM2.5 standards a reasonable
approach when considered in
conjunction with the regional haze
program as a means of achieving
appropriate levels of visibility
protection in urban, non-urban, and
Class I areas across the United States.
With regard to evaluating the safe
harbor increments for PM2.5, we had to
consider how much weight to give to
visibility protection as a function of the
increments. That is, whether the
increments were the appropriate means
of providing the most effective
protection against visibility impairment
in urban areas as well as in rural areas,
including Federal Class I areas. In light
of the other more direct approaches
being used to address visibility
problems across the United States, we
believe that the use of distinct PM
increments for visibility protection is
not the most effective means of
addressing the visibility problem. Thus,
we do not believe it is necessary to
modify the safe harbor increments for
PM2.5 to further protect visibility.
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3. Proposed Baseline Dates for PM2.5
Increments Under Option 1
based on the same technical evidence
that led us to revoke the annual PM10
NAAQS. As discussed earlier, we do not
If we adopt option 1, we propose to
require the implementation of the PM2.5 believe EPA is precluded from adopting
new particular matter increments under
increment system with new baseline
section 166(a) of the Act because we
areas, baseline dates and trigger dates.
promulgated a NAAQS for PM2.5 after
Specifically, we are proposing that the
1977. However, if we read section 166(f)
major source baseline date and trigger
date, both fixed dates, will be defined as to address PM10 alone, the interaction of
sections 166(a) and 166(f) could suggest
the effective date of this rule after
that pollutant-specific PSD regulations
promulgation.
In light of current and expected trends for PM promulgated on the basis of
in PM2.5 concentrations, EPA’s judgment section 166(a) must be limited to
regulations that address fine PM.
is that starting with new baseline dates
However, this view would create
on or after the effective date of this rule
tension with language in section 166(a)
would make the new PSD increments
that calls for us to conduct a holistic
more protective. Under our proposed
evaluation to establish a system of PSD
approach, any emissions reductions
regulations (including numerical and
occurring prior to the effective date of
other measures) for each pollutant
this rule would be counted toward the
covered by this provision. Since it
baseline concentration rather than
would be preferable to develop a system
expanding the PM2.5 increment. If a
of regulation for PM generally and select
retroactive baseline date were to apply,
the appropriate indicator for PM
emissions reductions occurring prior to
increments based on a comprehensive
the effective date of this rule would
review of the effects of all forms of PM
serve to expand the available
(as we did in the recent NAAQS rule),
increments, enabling more pollution
we do not believe Congress could have
than would otherwise be allowed to
intended to constrain EPA’s discretion
occur.
to consider the potentially differing
In addition, we believe starting with
effects of coarse and fine particles when
new baseline dates to implement new
developing pollutant-specific PSD
increments for PM2.5 is appropriate
regulations under section 166(a).
under this option because we would
Since EPA recently revised the
treat PM2.5 essentially as a ‘‘new’’
NAAQS for PM10 and eliminated the
pollutant for purposes of PSD and
annual PM10 NAAQS, we believe it is
section 166 of the Act. We believe that
permissible for the Agency to interpret
establishing a new baseline overcomes
the phrase ‘‘pollutants for which
significant implementation concerns
national ambient air quality standards
that would otherwise exist if the
are promulgated after August 7, 1977’’
existing PM baseline were maintained.
to apply to revisions to PM10 as well. In
If we were to require sources and
our 1989 proposal to adopt PM10
reviewing authorities to conduct PM2.5
increments, before the addition of
increment analyses based on the minor
section 166(f) to the Act, we construed
source baseline dates previously
the language in section 166(a) to be
established under the TSP or PM10
broad enough to support adoption of
program, they would have to attempt to
PM10 increments. Under a holistic
recreate the PM2.5 emissions inventory
approach, considering all forms of PM,
as of the minor source baseline date in
we do not believe the evidence supports
order to determine the baseline PM2.5
retaining an annual increment for PM10
concentration for the area. For early
under the PSD program. In our October
minor source baseline dates in
17, 2006 action on the PM NAAQS, the
particular (e.g., 1976 in areas of the
Administrator concluded that an annual
United States), establishing the
emissions inventory for PM2.5 would be coarse particle NAAQS was not
warranted at this time. 71 FR 61198–99.
extremely difficult, cumbersome and
The CD concluded that the available
potentially inaccurate because historic
evidence does not suggest an association
emissions inventories did not include
of adverse health effects with long-term
PM2.5 emissions. For all of these
exposure to coarse particles and the SP
reasons, we are proposing option 1 as
concluded there is no quantitative
our preferred option and request
comment on this contingent safe harbor evidence that directly supports an
annual standard. Id. at 61198. With
approach under option 1
respect to welfare effects, the evidence
4. Revocation of PM10 Annual
indicated that a short-term PM2.5
Increments
standard was the best approach for
If we use option 1 to adopt additional addressing visibility. Id. at 61280. For
increments for PM2.5, we propose to
non-visibility welfare effects, the
Administrator concluded that the
revoke the annual increments for PM10
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available evidence was not sufficient to
support an additional indicator, but that
a secondary NAAQS identical to the
primary NAAQS directionally improves
the level of protection afforded
vegetation, ecosystems, and materials.
Id. at 61210.
When the evidence described in the
Criteria Document and Staff Paper is
considered in light of the legal criteria
applicable under section 166(c), we
believe it supports the conclusion that
an annual PM10 increment is no longer
needed under the PSD program. In the
absence of a clear association between
long-term exposure to coarse particles
and adverse health effects, we do not
see a justification for an annual PM10
increment to protect public health,
notwithstanding compliance with the
NAAQS. In addition, the new
increments for PM2.5 that we propose to
adopt, in combination with the existing
24-hour increment for PM10, will
address welfare effects, air quality
related values, and air quality in
national parks and other special areas.
As described earlier, visibility impacts
are principally attributable to short-term
fine particle concentrations and thus
will be addressed by the new short-term
PM2.5 increment. The evidence indicates
that the non-visibility welfare effects of
concern are primarily attributable to
deposition of sulfate and nitrate
particles of any size. Thus, the
combination of the new PM2.5
increments and the existing 24-hour
PM10 increment will address nonvisibility welfare impact attributable to
deposition. Since we propose to retain
the 24-hour PM10 increment and adopt
new annual and 24-hour fine particle
increments that will target all of these
effects, we do not consider it warranted
to require continued tracking of changes
in annual concentrations of PM10 under
the PSD program.
B. Option 2—Equivalent Substitution
Approach for Annual Increments—
Section 166(f)
Under this option, we would
recognize PM2.5 as a new indicator for
PM for NSR purposes, and develop
annual PM2.5 increments to replace the
annual PM10 increments using the
equivalent substitution approach under
the authority of section 166(f) of the Act.
The approach proposed under this
option in this proposed rule would be
similar to the one we used in 1993, and
discussed earlier to convert from TSP
increments to PM10 increments, to avoid
having to implement increments based
on standards that no longer existed. On
October 17, 2006, EPA revoked the
primary and secondary annual PM10
standards and retained the primary and
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secondary 24-hour PM10 standards. 71
FR 61144.
In this case, we therefore are
developing annual PM2.5 increments to
replace the annual PM10 increments.
Also, consistent with our prior action in
1993, we are proposing to eliminate or
revoke the PM10 increments in this
notice. However, for developing the 24hour PM2.5 increments, we are
proposing to use the increment values
derived under the contingent safe
harbor approach explained in option 1.
We seek comment not only on the levels
of the proposed ‘‘equivalent’’
increments, but also on our use of this
equivalent increment option for only the
annual PM2.5 increments. In addition,
we seek comment on whether we
should rely on section 166(f) to also
propose the 24-hour PM2.5 increments,
even though the primary and secondary
24-hour PM10 NAAQS are not being
revoked.
1. Development of Equivalent
Increments
To establish equivalent PM10
increments in the 1993 rule, EPA
compared the TSP and PM10 impacts of
each of the 249 major sources subject to
major NSR in our NSR database. EPA
observed that, in principle, for any
source the equivalent PM10 increments
was simply the product of the TSP
increment to the source’s PM10/PM
emissions ratio. 58 FR 31627.
In this rulemaking, EPA proposes to
apply the same type of ratio approach to
establish equivalent increments for
PM2.5 under section 166(f) of the Act.
Unlike the 1993 analysis where we
evaluated a database of 249 major
sources, for this rulemaking EPA relied
on a more comprehensive analysis of
the ‘‘2001 National Emissions Estimates
by Source Categories’’ for PM10 and
PM2.5.17 From the 2001 National
Emissions Inventory, the ratio of
emission estimates from utilities and
industrial point source categories were
used to find the PM2.5 to the PM10
emissions ratio. For purposes of
deriving the ratio, area sources and nonroad and mobile sources were not
included on the basis that for NSR
permitting virtually all of the permitted
sources fall within the utility and
industrial point source categories.
Utilities and industrial point source
emission estimates were combined and
a ratio of 0.8 was calculated as the ratio
of emissions of PM2.5 to PM10. Hence,
the annual increments developed for
PM2.5 would be equal to 0.8 multiplied
by the increment value for PM10.
Although we believe that this approach
is based on a permissible interpretation
of the statute, we believe it results in
increment values for PM2.5 that are
much higher than the values Congress
envisioned when it established the
original increments for PM and SO2
based on percentages of the then
existing NAAQS. For example, an
annual PM2.5 increment in Class II areas
using this approach would be 13 µg/m 3,
which is 87 percent of the annual PM2.5
NAAQS of 15 µg/m 3. In contrast,
Congress established the Class II
Increments for PM and SO2 to represent
25 percent of the NAAQS. To avoid
such an unreasonable outcome for
PM2.5, we rejected this approach and
instead are proposing two variations
(options 2A & 2B) of the equivalent
increment approach as the second and
third option.
2. Proposed Annual Increments for
PM2.5
a. Option 2A
In addition to an emissions ratio to
reflect the shift in the indicator from
PM10 to PM2.5, we have also considered
the shift in the stringency of the NAAQS
that resulted when we changed the
pollutant indicator from PM10 to PM2.5.
Accordingly, the ratio of emissions (0.8)
that we previously calculated would be
multiplied by the ratio of the PM2.5
NAAQS over the PM10 NAAQS (15/50 =
0.3 µg/m 3 for the annual standard) to
derive an adjustment factor (0.24 for the
annual NAAQS) for calculating the
Class I, II, and III annual PM2.5
increments. Hence, multiplying the
Class I, II, and III annual PM10
increments, 4, 17, and 34 µg/m 3,
respectively, by the new adjustment
factor yields the following proposed
increment values (rounded to the
nearest whole number) under option
2A:
NAAQS
µg/m 3)
Averaging period
Annual ..............................................................................................................................................
24-hr .................................................................................................................................................
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Coincidentally, this new adjustment
based on the PM2.5-to-PM10 NAAQS
ratio results in annual PM2.5 increment
values identical to the values derived
using option 1, the percentage-ofNAAQS approach. As stated earlier,
because the 24-hour PM10 NAAQS have
not been revoked, we do not consider
section 166(f) to be the best fit for the
development of the 24-hour PM2.5
increments. Thus, for new 24-hour
PM2.5 increments, we are proposing to
rely on the authority of section 166(a) to
derive 24-hour increments as proposed
under option 1.
b. Option 2B
This option represents another
variation on the section 166(f)
equivalent increment approach. Under
this option 2B, we are proposing to
develop annual PM2.5 increments based
Increments
(µg/m 3)
Class I
15
35
Class II
1
2
Annual ..............................................................................................................................................
15
17 2001 National Emissions Estimates by Source
Categories.
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8
18
Increments
(µg/m 3)
Class I
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9
solely on the ratio of the annual PM2.5
NAAQS to the primary annual PM10
NAAQS (15/50 = 0.3 µg/m 3 for the
annual NAAQS). The values for the
annual PM2.5 increments derived by
multiplying the Class I, II, and III annual
PM10 increments, 4, 17, and 34 µg/m 3,
respectively, by this adjustment ratio
yields the following proposed increment
levels (rounded to the nearest whole
number) under option 2B:
NAAQS
(µg/m 3)
Averaging period
Class III
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Class III
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Increments
(µg/m 3)
NAAQS
(µg/m 3)
Averaging period
Class I
24-hr .................................................................................................................................................
As with option 2A, for the 24-hour
PM2.5 increments, we are proposing to
use increment values developed via the
contingent safe harbor approach as
described in option 1.
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3. Baseline Dates
Under these options (2A and 2B),
since we will be replacing annual PM10
increments with annual PM2.5
increments, we propose to retain the
existing TSP/PM10 baseline and trigger
dates and baseline areas for the PM2.5
program. Section 166(f) does not
address how EPA should handle
baseline dates for a substituted
increment. In 1993, we decided to retain
the existing baseline dates for TSP when
we replaced the section 163 increment
with PM10 increments. We propose the
same approach under this option in this
rulemaking because the continuation of
the historic TSP/PM10 baseline dates
would ensure that no past case of
increment consumption is abandoned
and serve as the closest measure of a
substitute. However, as discussed
earlier, given PM2.5 emissions trends,
our judgment is that establishing
baseline dates for PM2.5 after the
effective date of this rule may be more
effective at preventing significant
deterioration because the baseline
concentrations will reflect emissions
reductions. We request comment on
whether this would provide sufficient
justification for EPA to establish new
baseline dates under the section 166(f)
substitution approach.
However, in conjunction with the
annual PM2.5 increments discussed
above, we are proposing to use option
1 increment levels for 24-hour PM2.5
increments which would use new
baseline areas, trigger and baseline
dates. Thus, assuming the baseline date
for the PM10 increments has already
been triggered, this results in different
baseline dates for the annual and 24hour PM2.5 increments. This would also
require a PSD applicant to develop two
separate emissions inventories of
increment-consuming sources for
evaluating a new source’s cumulative
PM2.5 impacts in the area of concern. We
seek comment on this issue of multiple
inventories under the equivalent
increments approach.
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VI. Significant Impact Levels (SILs)
A. EPA’s Guidance on SILs in the PSD
Program
Significant Impact Levels or SILs are
numeric values derived by EPA that
may be used to evaluate the impact a
proposed major source or modification
may have on the NAAQS or PSD
increment. The SILs currently appear in
EPA’s regulations in 40 CFR 51.165(b),
which are the provisions that require
States to operate a preconstruction
review permit program for major
stationary sources that wish to locate in
an attainment or unclassifiable area but
would cause or contribute to a violation
of the NAAQS. The SILs in that
regulation are the level of ambient
impact that is considered to represent a
‘‘significant contribution’’ to
nonattainment.
Although 40 CFR 51.165 is the
regulation that establishes the minimum
requirements for nonattainment NSR
programs in SIPs, the provisions of 40
CFR 51.165(b) are actually applicable to
sources located in attainment and
unclassifiable areas. See 40 CFR
51.165(b)(4). Where a PSD source
located in such areas may have an
impact on an adjacent non-attainment
area, the PSD source must still
demonstrate that it will not cause or
contribute to a violation of the NAAQS
in the adjacent area. This demonstration
may be made by showing that the
emissions from the PSD source alone are
below the significant impact levels set
forth in 40 CFR 51.165(b)(2). However,
where emissions from a proposed PSD
source or modification would have an
ambient impact in a non-attainment area
that would exceed the SILs, the source
is considered to cause or contribute to
a violation of the NAAQS and may not
be issued a PSD permit without
obtaining emissions reductions to
compensate for its impact. 40 CFR
51.165(b)(2)–(3).
The EPA has also applied SILs in
other analogous circumstances under
the PSD program. Based on EPA
interpretations and guidance, SILs have
also been widely used in the PSD
program as a screening tool for
determining when a new major source
or major modification that wishes to
locate in an attainment or unclassifiable
area must conduct a more extensive air
quality analysis to demonstrate that it
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35
Class II
2
Class III
9
18
will not cause or contribute to a
violation of the NAAQS or PSD
increment in the attainment or
unclassifiable area. SILs are also used to
define the extent of the Significant
Impact Area (SIA) where a cumulative
air quality analysis accounting for
emissions changes from all sources in
the SIA is performed.
The EPA’s historical application of
SILs to the analysis of major source
impacts on attainment and
unclassifiable areas under the PSD
program has largely been based on
interpretations reflected in EPA
guidance memorandum. The EPA has
not previously incorporated the concept
of a SIL into our PSD regulations at 40
CFR 51.166 and 40 CFR 52.21.
Nevertheless, EPA has long considered
the ‘‘significant contribution’’ test set
forth in 40 CFR 51.165(b)(2) to apply to
the impact of PSD sources on attainment
areas as well, since that provision
applies to major new sources and major
modifications located in attainment and
unclassifiable areas. Thus, EPA has also
supported the use of SILs as screening
mechanism when analyzing whether a
source located in a PSD area will cause
or contribute to a violation of the
NAAQS or PSD increment in attainment
or unclassifiable areas.
Although EPA’s current PSD
regulations do not contain SILs, EPA
initially developed SILs for TSP and
other pollutants under the PSD program
in 1978. 43 FR 26380 (June 19, 1978).
In the preamble to our 1978 regulations,
EPA described SILs as a screening
technique to alleviate resource burdens
(the costs and time involved in
sophisticated computer modeling of
ambient air impacts) where there was
little or no threat to the PSD increments
or NAAQS. 45 FR 26398. However, as
the threat to the increments increased,
EPA intended for more sophisticated
techniques to be used. Id. Since EPA’s
analysis indicated that the air quality
impact of many sources fell off rapidly
to insignificant levels, the Agency did
not intend to analyze the impacts
beyond the geographic point where the
concentrations from the source fell
below certain levels derived from the
class I increments. Id. These levels were
interpreted by EPA as representing the
minimum amount of ambient impact
that is significant and hence came to be
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known as the significant impact levels
or SILs. Id.
When EPA substantially revised our
PSD regulations in 1980 to include
significant emissions rates and
significant monitoring concentrations,
EPA did not include the SILs in our PSD
regulations. At that time, EPA felt that
there was no need for a separate table
of SILs because of the adoption of ‘‘a de
minimis exclusion for monitoring’’
otherwise known as SMCs (described
later). 45 FR 52707. In addition, EPA
saw little value in retaining SILs as an
exemption from the air quality analysis
because the demonstration necessary to
qualify for the exemption was itself an
air quality analysis. 45 FR 52707.
Subsequently, in draft guidance for
permit writers, EPA advised that SILs
may be used to determine whether a
source needs to conduct a cumulative or
‘‘full’’ impact analysis to demonstrate
that in conjunction with all other
increment consuming sources, it will
not cause or contribute to violation of
the NAAQS or PSD increment in an
attainment or unclassifiable areas. New
Source Review Workshop Manual, at
C.24-C.25 (Draft 1990); See also 40 CFR
51.166(k); 40 CFR 52.21(k). Permitting
authorities followed this guidance, and
this approach remains an accepted
aspect of PSD program implementation.
If based on a preliminary impact
analysis, a source can show that its
emissions alone will not increase
ambient concentrations by more than
the SILs, EPA considers this to be a
sufficient demonstration that a source
will not cause or contribute to a
violation of the NAAQS or increment.
In light of the unique air quality
considerations in Class I areas, EPA has
drawn a distinction between the use of
SILs in Class II areas and Class I areas.
The EPA’s draft 1990 guidance only
identified SILs to be used in Class II
areas under the PSD program. Workshop
Manual at C.28. However, in 1991, EPA
advised the State of Virginia that the
concept of a SIL might be applied to
Class I areas if the levels were
determined in a reasonable manner.
Memorandum from John Calcagni, Air
Quality Management Division, to
Thomas J. Maslany, Air, Radiation, and
Toxics Divisions (Sept. 10, 1991). The
EPA did not support the use of SILs to
determine whether a source should
conduct an analysis of its impact on airquality related values (AQRVs). Since
there are currently no Class III areas for
PSD in the United States, there has been
no need for EPA to apply SILs in these
areas.
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B. Legal Basis for SILs
The concept of a significant impact
level is grounded on the de minimis
principles described by the court in
Alabama Power Co. v. Costle, 636 F.2d
323, 360 (D.C. Cir. 1980). In this case
reviewing EPA’s 1978 PSD regulations,
the court recognized that ‘‘there is likely
a basis for an implication of de minimis
authority to provide exemption when
the burdens of regulation yield a gain of
trivial or no value.’’ 636 F.2d at 360.
Based on this de minimis principle from
the court’s opinion, EPA developed
significant emissions rates and
significant monitoring concentrations in
our 1980s regulations for PSD. The
significant emission rates reflect levels
below which EPA considers an
emissions increase to be de minimis and
thus not a major modification that
requires a PSD permit or NA–NSR
permit. 45 FR 52676, 52705–07. See also
40 CFR 51.166(b)(23); 40 CFR
52.21(b)(23). As discussed further later,
the significant monitoring
concentrations in EPA regulations
define a de minimis level of impact that
EPA has concluded does not justify
collecting pre-construction monitoring
data for purposes of an air quality
impact analysis. 45 FR 52710.
Similarly, significant impact levels
are intended to identify a level of
ambient impact on air quality
concentrations that EPA regards as de
minimis. The EPA considers a source
whose individual impact falls below a
SIL to have a de minimis impact on air
quality concentrations. Thus, a source
that demonstrates its impact does not
exceed a SIL at the relevant location is
not required to conduct more extensive
air quality analysis or modeling to
demonstrate that its emissions, in
combination with the emissions of other
sources in the vicinity, will not cause or
contribute to a violation of the NAAQS
at that location. In light of insignificance
of the ambient impact from the source
alone, EPA considers the conduct of a
cumulative air quality analysis and
modeling by such a source to yield
information of trivial or no value with
respect to the impact of the proposed
source or modification. The EPA’s
Environment Appeals Board has
recently reiterated and affirmed EPA’s
interpretation of the Act to allow EPA
to evaluate the significance of a source’s
impact when determining whether it
would ‘‘cause or contribute’’ to a
NAAQS or increment violation under
section 165(a)(3) of the Act. In Re:
Prairie State Generating Company, PSD
Appeal No. 05–05, slip op. at 139–144
(Aug. 24, 2006).
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54139
Thus, in developing SILs for this
proposal, EPA sought to derive SILs for
PM2.5 utilizing methods that would
identify levels representing a de
minimis or insignificant impact on
ambient air quality. In choosing among
the options set forth later, EPA proposes
to select an option that reflects the
degree of ambient impact on PM2.5
concentrations that can be considered
truly de minimis and would justify no
further analysis or modeling of the air
quality impact of a source in
combination with other sources in the
area because the source would not cause
or contribute to an exceedance of the
PM2.5 NAAQS or the PM2.5 increments
established elsewhere in this proposal.
C. Relationship of SILs to AQRVs
We wish to emphasize that consistent
with the original purpose of the Class I
SILs, the Class I SILs for PM2.5 we are
proposing are not intended to serve as
thresholds for determining the need for
an AQRV analysis or whether an
adverse impact on an AQRV will occur.
An adverse impact on an AQRV
depends upon the sensitivity of the
particular AQRV. An ambient
concentration that is considered
insignificant for purposes of increment
consumption should not automatically
be considered inconsequential relative
to the inherently fact-specific
demonstration upon which an adverse
impact on an AQRV is to be based.
Accordingly, the fact that a source’s
predicted impact is less than the SIL in
a Class I area would neither relieve the
source from having to complete an
analysis of impacts on AQRVs nor
automatically allow the reviewing
authority to reject the FLM’s
demonstration of adverse impact on an
AQRV. See 61 FR at 38292.
D. Proposed Options for PM2.5 SILs (for
PSD and NA–NSR)
We are seeking comment on the
relative merits of each of the following
options for setting PM2.5 SILs.
1. Option 1. Propose SILs Using the
Approach We Proposed for PM10 in
1996
The first option that we are proposing
utilizes the same approach we proposed
for PM10 in the 1996 NSR Reform
proposal. For Class I areas we would set
the SIL to 4 percent of the Class I PM2.5
increment. For Class II and Class III
areas, we would codify the SIL values
of 1.0 µg/m 3 for the annual averaging
period and 5.0 µg/m 3 for the 24-hour
averaging period, that already exist for
PM10 in 40 CFR 51.165(b)(2). If we adopt
this option, we would set the Class I
SILs based on the Class I increments
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that we elect to adopt under the
increment options. Based on the Class I
increment values proposed in the
percent of NAAQS increment option 1,
the SILs under this option would be as
follows:
Class I
increment
(µg/m 3)
Averaging period
Annual ..............................................................................................................................................
24-hour .............................................................................................................................................
As stated earlier, we had proposed
this approach for setting PM10 SILs in
our 1996 NSR Reform proposal. Many
commenters supported this approach
and believed that the proposed SIL
values would serve as appropriate de
minimis values. In fact, EPA is aware
that many States have been using these
proposed SILs for PM10 as screening
tools since 1996.
Regarding the proposal to set the level
of Class I SILs at 4 percent of the Class
I increments, we believe that where a
proposed source contributes less than 4
percent to the Class I increment,
concentrations are sufficiently low so as
not to warrant a detailed analysis of the
combined effects of the proposed source
and all other increment-consuming
emissions. We previously used a similar
rationale to establish the significant
emissions rates for PSD applicability
purposes, concluding in part that
emissions rates that resulted in ambient
impacts less than 4 percent of the 24hour standards for PM and SO2 were
sufficiently small so as to be considered
de minimis.
The original SIL values of 1.0 and 5.0
µg/m 3 for TSP and PM10 were
interpreted by EPA as representing the
minimum amount of ambient impact
that is significant. This forms the basis
of the proposed PM2.5 SIL values of 1.0
and 5.0 µg/m 3 for the annual and 24hour standard for Class II and III areas.
SILs
(µg/m 3)
Class I
1
2
0.04
0.08
Class II
Class III
1.0
5.0
1.0
5.0
2. Option 2. PM2.5 to PM10 Emissions
Ratio
In our second proposed option for
SILs, we would multiply the PM10 SILs
(proposed in 1996) by the emissions
ratio of PM2.5 to PM10 for point sources
in the 2001 extrapolation of the final
1999 NEI. This is very similar to option
2A for developing increments, and
would use the same PM2.5/PM10
emissions ratio (0.8). The Class I PM10
SILs that we proposed in 1996 were 0.2
µg/m3 (annual) and 0.3 µg/m 3 (24-hour).
For Class II and III PM10 SILs, we
proposed 1.0 µg/m 3 (annual) and 5.0 µg/
m 3 (24-hour) levels. The SIL values
determined in this option are as follows:
SILs (µg/m3)
Averaging period
Class I
Annual ..................................................................................................................................................................
24-hour .................................................................................................................................................................
The SILs derived under this option
are slightly more stringent for Class II &
III areas than those in option 1. Since
PM2.5 emissions are a subset of PM10
emissions, we believe that an emissions
ratio of the PM10 SILs would serve as an
appropriate de minimis SIL value and
represent insignificant impact on
ambient air quality.
3. Option 3. PM2.5 to PM10 NAAQS Ratio
Under the third option that we are
proposing, we would multiply the PM10
SILs by the ratio of the PM2.5 NAAQS
to the PM10 NAAQS. This is very similar
0.16
0.24
Class II
0.8
4.0
Class III
0.8
4.0
to option 2B for developing PM2.5
increments, and would use the same
factors. We would start with the same
values for the PM10 SILs that we used
for option 2 above for SILs. The PM2.5
SILs determined using this approach are
as follows:
SILs (µg/m3)
Averaging period
Class I
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Annual ..................................................................................................................................................................
24-hour .................................................................................................................................................................
The SILs derived under this option
are very stringent for Class II and III
areas compared to options 1 and 2.
Nevertheless, we believe that the
NAAQS ratio approach is an
appropriate alternative to determine
SILs, since it reflects the stringency in
the NAAQS for PM2.5 relative to that of
PM10. We believe that these SIL values
would serve as appropriate de minimis
values.
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VII. Significant Monitoring
Concentrations (SMCS)
A. Background on SMCs
1. Preconstruction Monitoring and Its
Role in NSR Program
Under the Act and EPA regulations,
an applicant for a PSD permit is
required to gather preconstruction
monitoring data in certain
circumstances. Section 165(a)(7) calls
for ‘‘such monitoring as may be
necessary to determine the effect which
emissions from any such facility may
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0.06
0.07
Class II
0.3
1.2
Class III
0.3
1.2
have, or is having, on air quality in any
areas which may be affected by
emissions from such source.’’ 42 U.S.C.
7475(a)(7). In addition, section 165(e)
requires an analysis of the air quality in
areas affected by a proposed major
facility or major modification and calls
for gathering 1 year of monitoring data
unless the reviewing authority
determines that a complete and
adequate analysis may be accomplished
in a shorter period. 42 U.S.C. 7575(e)(3).
These requirements are codified in
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EPA’s PSD regulations at 40 CFR
51.166(m) and 40 CFR 52.21(m).
In accordance with EPA’s Guideline
for Air Quality Modeling (40 CFR part
51, Appendix W), the preconstruction
monitoring data is primarily used to
determine background concentrations in
modeling conducted to demonstrate that
the proposed source or modification
will not cause or contribute to a
violation of the NAAQS. 40 CFR part 51,
Appendix W, section 9.2. For most areas
where multiple sources of air pollution
are present, EPA’s Guideline
recommends using monitoring data to
identify the portion of background
concentrations attributable to natural
background, minor sources, and distant
major sources. 40 CFR part 51,
Appendix W, section 9.2.3.f. For nearby
major sources, EPA recommends
explicitly modeling the emissions of
such sources rather than relying on
monitored data as part of the NAAQS
compliance demonstrations. As
described earlier, the compliance
demonstration with respect to the PSD
increment compliance focuses on
modeling the change in emissions from
sources in the Significant Impact Area.
2. History of SMC Rules Adopted by
EPA
In 1980, EPA adopted regulations that
exempt sources from preconstruction
monitoring requirements for a pollutant
if the source can demonstrate that its
ambient air impact is less than a value
known as the Significant Monitoring
Concentration or SMC. The pollutantspecific SMCs are codified at 40 CFR
51.166(i)(5)(i) and 40 CFR 52.21(i)(5)(i).
The EPA developed SMCs as a
screening tool for sources to determine
whether they should conduct sitespecific preconstruction ambient
monitoring. At the time they were
adopted, EPA described the SMCs as
‘‘air quality concentration de minimis
level[s] for each pollutant * * * for the
purpose of providing a possible
exemption from monitoring
requirements.’’ 45 FR 52676, 52707
(Aug. 7, 1980). The EPA explained that
it believed there was ‘‘little to be gained
from preconstruction monitoring’’
where a source could show that its
projected impact on the affected area
was below these de minimis levels. 45
FR 52710.
In 1980, EPA determined the SMCs
based on the current capability of
providing a meaningful measure of the
pollutants. The EPA promulgated values
that represented five times the lowest
detectable concentration in ambient air
that could be measured by the
instruments available for monitoring the
pollutants. 45 FR 52710. The EPA chose
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the factor of five after reviewing test
data for various methods and
considering instrument sensitivity,
potential for sampling error, instrument
variability, and the capability to read
recorded data. Id.
For PM, EPA set the SMCs for TSP at
five times the lowest detectable ambient
concentration for TSP (2.0 µg/m 3) using
the Reference Method 5 for ambient
sampling at that time. Memorandum
from Rehme, K. A., EPA/EMSL/QAD/
MSB, to Peters, W., EPA/OAQPS/CPDD,
on PSD Monitoring (May 20, 1980). We
set a SMC only for the 24-hour
averaging period, at a level of 10 µg/m 3.
We retained the same numerical level
when we replaced the TSP NAAQS and
increments with the PM10 NAAQS and
increments.
B. Legal Basis for SMCs
As with the SMCs adopted by EPA in
1980, the SMCs for PM2.5 proposed in
this action are supported by the de
minimis doctrine set forth in the
Alabama Power v. Costle opinion. Like
the other pollutants for which EPA has
promulgated SMCs, EPA believes there
is little to be gained from
preconstruction monitoring of PM2.5
concentrations when the increased
emissions of PM2.5 from a proposed
source or modification has a de minimis
impact on ambient concentrations of
PM2.5. If a source can show through
modeling of its emissions alone that its
impacts are less than the corresponding
SMC, there is little to be gained by
requiring that source to collect
additional monitoring data on PM2.5
emissions to establish background
concentrations for further analysis.
Therefore, in developing SMCs for
this proposal, EPA sought to use
methods that would identify levels
representing a de minimis or
insignificant impact on PM2.5 ambient
air quality that makes the collection of
additional monitoring data extraneous.
In choosing among the options set forth
later, EPA proposes to select an option
that reflects the degree of ambient
impact on PM2.5 concentrations that can
be considered truly de minimis and
would not justify the gathering of
monitoring data to establish background
concentrations for a demonstration of
compliance with the NAAQS.
C. Proposed Options for PM2.5 SMC
1. Option 1. Lowest Detectable
Concentration
For this approach, we would use the
same methodology originally used in
1980 to set the SMC for TSP, i.e.,
determining the lowest detectable
concentration and multiplying this
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54141
value by five. The lowest detectable 24hour average concentration for PM2.5 is
2.0 µg/m 3 (40 CFR 50 App L, section 3).
Thus, applying this methodology for
PM2.5 yields an SMC of 10 µg/m 3 for the
24-hour averaging period.
As we indicated in 1980 when we
originally used this methodology to set
the SMCs for TSP and the other PSD
pollutants, the use of five times the
lowest detectable concentration was
chosen to realistically reflect pollutant
levels at which low level concentrations
or small incremental changes in
pollutant concentrations can reasonably
be determined. The factor of five takes
into account the measurement errors
associated with the monitoring of these
low pollutant levels or small
incremental changes in concentration.
These measurement errors arise from
various sources, such as sample
collection, analytical measurement,
calibration, and interferences (See
Memorandum from Rehme, K. A.
mentioned earlier). We believe this is a
reasonable approach, since it has also
been used for PM2.5 and TSP. We seek
comment on this approach.
2. Option 2. PM2.5 to PM2.5 Emissions
Ratio
Proposed option 2 establishes the
SMC for PM2.5 by multiplying the
existing PM10 SMC (10 µg/m 3) by the
ratio of PM2.5 emissions to PM10
emissions in the 2001 extrapolation of
the final 1999 NEI. This is the same
methodology used in Increments option
2A and SIL option 2, and uses the same
emissions ratio (0.8). This yields a SMC
value of 8.0 µg/m 3 for PM2.5 for the 24hour averaging period.
This approach gives a PM2.5 SMC
value that is equivalent, in terms of
emissions, to the existing PM10 SMC.
We believe that this approach is
consistent with the approach that
Congress set out for increments in
section 166(f) of the Act and is, as such,
a reasonable approach for developing
PM2.5 SMCs. We seek comment on this
approach.
3. Option 3. PM2.5 to PM10 NAAQS Ratio
Under the third option, we propose to
multiply the PM10 SMC by the ratio of
the PM2.5 NAAQS to the PM10 NAAQS.
This is the same approach proposed for
Increment option 2B and SIL option 3.
Because the PM10 SMC is for the 24hour averaging period, we would use
the ratio of the 24-hour NAAQS for
PM2.5 (35 µg/m 3) and PM10 (150 µg/m 3).
The resulting factor is 0.233. Thus, the
PM2.5 SMC developed using this option
would be 2.3 µg/m 3, for the 24-hour
averaging period.
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The SMC developed using this
approach is very stringent compared to
options 1 and 2, since it reflects the
stringency of the 24-hour NAAQS of
PM2.5 relative to PM10. Nevertheless, we
believe this to be also a reasonable
approach and seek comments on it.
D. Correction of Cross References
In addition to exempting sources that
have emissions increases below the
SMCs, EPA also exempts sources from
preconstruction monitoring where the
source demonstrates that existing
ambient concentrations of a pollutant in
the affected area are currently below the
SMCs. 40 CFR 51.166(i)(5)(ii);
52.21(i)(5)(ii). This aspect of the
monitoring exemption was also adopted
in the 1980 rulemaking. 45 FR 52710.
The EPA also proposes in this
rulemaking to correct a cross reference
contained in these parts of the
regulations. Paragraphs (ii) and (iii) in
40 CFR 51.166(i)(5) and paragraph (ii) in
40 CFR 52.21(i)(5) each refer to
concentrations listed in paragraphs
(i)(8)(i). However, there is no paragraph
(i)(8)(i) in § 51.166 and no concentration
values are contained in section (i)(8)(i)
of § 52.21. The cross references in these
provisions were intended to reference
the SMCs in paragraph (i)(5)(i), but EPA
failed to make this change when the
paragraphs were renumbered in a prior
rulemaking. We propose to correct that
oversight in this rule.
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VIII. Effective Date of the Final Rule,
SIP Submittal/Approval Deadlines and
PM10 Revocation Deadline
This section sets forth EPA’s proposed
effective dates for the PM2.5 increments
(under different options), SILs and SMC.
In addition, we are setting forth the
proposed deadlines for States to submit
revisions to their SIPs incorporating
these changes to the PSD regulations,
and for EPA to approve or disapprove
the revised plans. Finally, this section
describes EPA’s proposed schedule for
revoking the PM10 annual increments in
conjunction with the commencement of
the PM2.5 increment system under the
part 51 and part 52 PSD regulations and
we request comment on establishing a
transition period for processing
complete permit applications. Please see
Table 1 in the docket (Docket ID No.
EPA–HQ–OAR–2006–0605) for a
summary of the proposed options and
alternatives on which we seek comment.
A. Option 1: Increments Promulgated
Pursuant to Section 166(a) of the Act
1. Effective Date of Final Rule
As described in section III.E.2.a of this
preamble, section 166(b) of the Act
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specifies that new regulations for
increments promulgated pursuant to
section 166(a) of the Act become
effective 1 year after the date of
promulgation. Accordingly, if we
promulgate the new PM2.5 increment
under the authority of Section 166(a)
following Option 1, we propose a year’s
delay in the effective date.
Alternatively, EPA seeks comments
on whether we could make the new
increment regulations effective 60 days
from promulgation. Considering the
various timeframes outlined in section
166, it is clear that Congress envisioned
that increments or other measures
would become effective within 3 years
of the promulgation of a NAAQS. In the
current circumstance, due to prolonged
litigation and other implementation
concerns, there has been an extended
delay of over 10 years since we
established the PM2.5 NAAQS. Given
this extended delay, we believe that the
overall Congressional intent reflected in
section 166 may best be met by
advancing the effective date of the
proposed regulations.
States have to submit SIPs by April 5,
2008 to address the NSR provisions of
the final PM2.5 implementation rule
after the Federal NSR implementation
rule is promulgated later this year. If
EPA decides to promulgate option 1 for
increments and section 166(b) timelines,
the increments rule would not be
implemented in SIP-approved States
until approximately January 2010
(assuming promulgation of this rule in
Spring 2008 and allowing 21 months for
SIP submittal). Thus from April 2008 to
January 2010, PSD sources would be
subject to a PM2.5 applicability program,
but would need to continue the current
PM10 air quality impacts analysis. Under
these circumstances, we expect that
States, affected industry, and
environmental groups will see value in
advancing the effective date of the
promulgated increments.
Legislative history indicates that,
when section 166(b) was first enacted in
1977, Congress established the delayed
effective date in order to allow time for
‘‘contrary Congressional action.’’ H.R.
Conf. Rep. 95–564, at 151 (1977). The
Congressional Review Act (CRA)
provides Congress with an expedited
means of reviewing and potentially
disapproving final actions issued by
Federal agencies. Under the CRA, a
member of Congress can introduce a
joint resolution to disapprove a
particular rule and have that resolution
considered using expedited procedures
if the resolution is introduced within
the designated time period (generally 60
days depending on the Congressional
calendar). Furthermore, an agency rule
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meeting the CRA definition of ‘‘major’’
cannot take effect for 60 days. We
request comment on whether, given
these procedures under the CRA, a 60day delay in the effective date of the
proposed rule could satisfy the
Congressional intent reflected in section
166(b).
2. State Program
In this action, we propose to establish
final PM2.5 increments as minimal
program element for all State Programs.
Accordingly, States must submit revised
SIPs for EPA’s approval that incorporate
the final PM2.5 increments, or
demonstrate that an alternative
approach is at least equivalent to this
minimum program element. Irrespective
of whether we establish an effective date
of the final rule that falls 1 year after or
60 days after we promulgate the final
rule, we propose to require States to
submit revised implementation plans to
EPA for approval within 21 months of
promulgation (9 months after the
effective date of such regulations) in
accordance with the time frames
specified in section 166(b) of the Act.
Section 166(b) also specifies that we
must approve or disapprove these
revisions within 25 months of
promulgation (4 months from the
statutory deadline for SIP submittal).
We regard these statutory deadlines as
maximum allowed timeframes for action
and do not believe that the Act restricts
our ability to approve SIP revisions
requested by a State at any time before
these deadlines. We also propose to
change the regulatory provisions at 40
CFR 166(a)(6) to specifically articulate
these deadlines for these State SIP
submittals.
3. Federal Program
The EPA must also decide how to
apply the procedures set forth in section
166(b) of the Act to the new PM2.5
increments under our 40 CFR part 52
PSD regulations, which apply for States
without approved PSD programs as well
as for Indian lands. We propose to begin
to implement the Part 52 PSD program
upon the effective date of the final rule.
Accordingly, if we delay the effective
date for 1 year after the date of
promulgation in accordance with
Section 166(b), then the Part 52 PSD
program would become effective and
implemented in the applicable areas, on
this date. Alternatively, if we establish
an effective date 60 days after we
promulgate the final rules, the Part 52
PSD program would become effective on
this same date.
Alternatively, we request comment on
whether we should delay
implementation of the Federal Part 52
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PSD program until 25 months after
promulgation, or the outside date by
which EPA is required to approve State
SIP revisions. This is the same approach
we took in 1988 to implement the then
new NO2 increments. 53 FR at 40658.
We are not offering this as our proposed
approach because of the significant
delay that has already occurred between
the time we promulgated the PM2.5
NAAQS and the time we will finalize
this rule. However, we recognize that it
may not be equitable to begin
implementation of the new program
requirements in those few areas where
the Federal program applies before the
majority of States are required to
implement the program. Nonetheless,
we seek comment on applying this
alternative approach for the Federal Part
52 PSD program and specifically on the
consequences of potential inequities.
B. Option 2: Increments Promulgated
Pursuant to Section 166(f) of the Act
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1. Effective Date of Final Rule
In contrast to the proposed delay of
the effective date of the new PM2.5
increments under option 1, we propose
to make the new PM2.5 increments
proposed under option 2 effective 60
days from the date of promulgation,
consistent with the CRA timeframe. We
do not interpret section 166(b) of the
Act to apply to increments promulgated
under the authority of section 166(f)
because the first sentence in section
166(b) describes only ‘‘[r]egulations
referred to in subsection (a).’’
2. State Program
We previously stated that we believe
that it is appropriate to establish a
deadline for States to submit required
SIP revisions analogous to the deadline
that applies to States when we
promulgate or revise a NAAQS. 67 FR
80241. We previously codified,
conforming regulatory text at 40 CFR
166(a)(6). Under Option 2 of this
proposal, we propose to follow the
existing regulatory provisions that
require a State to adopt and submit for
EPA approval its PM2.5 plan revisions
no later than 3 years after the date on
which we promulgate (i.e., publish in
the Federal Register) the new
regulations in the 40 CFR part 51 PSD
regulations. Alternatively, we request
comment on whether we should require
a timeframe shorter than 36 months,
such as the statutory maximum of 21
months required under Option 1. Given
the limited nature of the required
changes, we believe that States generally
may not need more than 21 months to
adopt and submit revised plans to EPA
for approval. If we select this alternative
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approach, we propose to make
conforming regulatory changes to 40
CFR 166(a)(6).
3. Federal Program
For the Federal part 52 PSD
regulations, we propose under Option 2
to make the new PM2.5 increments
effective 60 days from the date we
promulgate the final rules. However,
unlike the proposed 3-year period being
proposed for States to submit their plan
revisions to EPA for review and
approval, we propose to implement the
new increments under the part 52 PSD
regulations upon the effective date of
the final rules. Since it would be
difficult to know when States are
planning to revise their own PSD
programs consistent with the new
increment regulations, it is not possible
to ensure a consistent implementation
date between approved State programs
and programs being implemented under
the part 52 PSD regulations unless we
delayed implementation for a full 4
years (3 years for SIP submission and 1
year for EPA to approve the revision).
We believe that this delay is excessive
and does not accomplish the goal of
expedient implementation of a PM2.5
PSD program. We request comment on
this approach.
C. Revocation of the PM10 Increment
While we believe it is appropriate to
revoke the annual PM10 increment as
explained earlier in this preamble, we
propose to retain the PM10 increments
in both 40 CFR part 51 and part 52 PSD
regulations until the new PM2.5
increments are being implemented
either by a State through an approved
SIP, or by EPA through the Federal Part
52 PSD program. Accordingly, we
propose to approve the removal of the
annual PM10 increments from any SIP
on or after the date we approve the new
PM2.5 increments in the same plan. We
believe that States should request the
removal of the annual PM10 increments
from their PSD programs at the same
time they submit plan revisions
containing the new PM2.5 increments,
allowing EPA to act on both actions
simultaneously.
Similarly, we propose to retain the
annual PM10 increments in the Part 52
PSD regulations until the effective date
of the new PM2.5 increments.
D. Transition Period
We believe that it is appropriate to
establish a transition period to clarify
when PSD permit applications must
contain an increment analysis for the
new PM2.5 increments following the
date they become effective and are
approved as part of any State or Federal
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54143
PSD program. In the past, we have
allowed for permit applications
submitted before the implementation
date of new increment regulations to
continue to be processed under the
existing rules, so long as the reviewing
authority has determined that the
application is complete before the
implementation date. See e.g., existing
40 CFR 51.166(a)(i)(8) and (9).
Consequently, we are also proposing a
new provision in both the 40 CFR parts
51 and 52 PSD regulations to provide a
transition process for initiating the
requirement for analysis of the new
PM2.5 increments. Under the Part 51
regulations, we are proposing that
during the transition period, States have
discretion to continue the existing PM10
increment program or begin
implementing the new PM2.5 increment
program. For the federally administered
programs under the Part 52 PSD
regulations, the provision would apply
to each new PSD permit applicant upon
the effective date of the rule. However,
we are also proposing a similar
transition period in these programs. See
proposed 40 CFR 51.166(i)(10) and 40
CFR 52.21(i)(11), respectively.
E. Effective Date for SILs and SMCs
Unlike the approach we propose for
PM2.5 increments, we are not proposing
to make SILs and SMCs a minimum
element of an approved SIP.
Accordingly, we are not proposing to
establish specific deadlines for
submission of revisions to incorporate
the final rules into SIPs. We do not
believe that SILs or SMCs are required
elements of an approvable State
program because in the absence of these
requirements, States can satisfy the
statutory requirements by obtaining preconstruction monitoring data and
conducting a cumulative air quality
analysis for every PSD permit
application.
Nonetheless, we believe that
availability of SILs and SMCs greatly
improve program implementation by
streamlining the permit process and
reducing the labor hours necessary to
submit and review a complete permit
application where the projected impact
of the proposed source is de minimis in
the relevant area. For these reasons, we
request comment on whether we have
authority to establish these as minimum
program elements based on the
improved efficiency of the permit
process. If we require States to
incorporate SILs and SMCs as
mandatory elements of an approvable
program, then we would apply the
existing regulations at 40 CFR 166(a)(6)
for establishing the SIP submittal
deadline. Under either approach, the
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final rules would become effective 60
days after we promulgate the final rules.
IX. Statutory and Executive Order
Reviews
A. Executive Order 12866: Regulatory
Planning and Review
Under Executive Order 12866 (58 FR
51735, October 4, 1993), this action is a
significant regulatory action because it
raises novel legal or policy issues
arising out of legal mandates, the
President’s priorities, or the principle
set forth in the EO. Accordingly, EPA
submitted this action to the Office of
Management and Budget (OMB) for
review under EO 12866 and any
changes made in response to OMB
recommendations have been
documented in the docket for this
action.
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B. Paperwork Reduction Act
The information collection
requirements in this rule have been
submitted for approval to the OMB
under the Paperwork Reduction Act, 44
U.S.C. 3501 et seq. The information
collection requirements are not
enforceable until OMB approves them.
The Information Collection Request
(ICR) document prepared by EPA has
been assigned EPA ICR number 2276.01.
Certain records and reports are
necessary for the State or local agency
(or the EPA Administrator in nondelegated States), for example, to: (1)
Confirm the compliance of status of
stationary sources, identify any
stationary sources not subject to the
standards, and identify stationary
sources subject to the rules; and (2)
ensure that the stationary source control
requirements are being achieved. The
information would be used by EPA or
State enforcement personnel to (1)
Identify stationary sources subject to the
rules, (2) ensure that appropriate control
technology is being properly applied,
and (3) ensure that the emission control
devices are being properly operated and
maintained on a continuous basis.
The proposed rule would increase the
PSD permitting burden for owners and
operators of major stationary sources of
PM2.5 emissions by adding PM2.5 to the
list of regulated NSR pollutants for
which air quality impact analyses must
be carried out to track increment
consumption and demonstrate
compliance with the NAAQS. At the
same time, there would be a reduction
in burden directly associated with the
revocation of the annual increment for
PM10, as proposed in this proposed rule.
Over the 3-year period covered by the
ICR, we estimate an average annual
burden totaling about 14,000 hours and
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$920,000 for all industry entities that
would be affected by the proposed rule.
For the same reasons, we also expect the
proposed rule (when fully
implemented) to increase burden for the
State and local authorities reviewing
PSD permit applications. In addition,
there would be additional burden for
State and local agencies to revise their
SIPs to incorporate the proposed
changes. Over the 3-year period covered
by the ICR, we estimate that the average
annual burden for all State and local
reviewing authorities will total about
4,150 hours and $180,000.
Burden means the total time, effort, or
financial resources expended by persons
to generate, maintain, retain, or disclose
or provide information to or for a
Federal agency. This includes the time
needed to review instructions; develop,
acquire, install, and utilize technology
and systems for the purposes of
collecting, validating, and verifying
information, processing and
maintaining information, and disclosing
and providing information; adjust the
existing ways to comply with any
previously applicable instructions and
requirements; train personnel to be able
to respond to a collection of
information; search data sources;
complete and review the collection of
information; and transmit or otherwise
disclose the information.
Any agency may not conduct or
sponsor, and a person is not required to
respond to a collection of information
unless it displays a currently valid OMB
control number. The OMB control
numbers for EPA’s regulations in 40
CFR are listed in 40 CFR part 9.
To comment on the Agency’s need for
this information, the accuracy of the
provided burden estimates, and any
suggested methods for minimizing
respondent burden, including the use of
automated collection techniques, EPA
has established a public docket for this
ICR under Docket ID number EPA–HQ–
OAR–2007–0628. Submit any comments
related to the ICR for this proposed rule
to EPA and OMB. See ‘Addresses’
section at the beginning of this notice
for where to submit comments to EPA.
Send comments to OMB at the Office of
Information and Regulatory Affairs,
Office of Management and Budget, 725
17th Street, NW., Washington, DC
20503, Attention: Desk Office for EPA.
Since OMB is required to make a
decision concerning the ICR between 30
and 60 days after September 21, 2007,
a comment to OMB is best assured of
having its full effect if OMB receives it
by October 22, 2007. The final rule will
respond to any OMB or public
comments on the information collection
requirements contained in this proposal.
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C. Regulatory Flexibility Act
The Regulatory Flexibility Act (RFA)
generally requires an agency to prepare
a regulatory flexibility analysis of any
rule subject to notice and comment
rulemaking requirements under the
Administrative Procedure Act or any
other statute unless the agency certifies
that the rule will not have a significant
economic impact on a substantial
number of small entities. Small entities
include small businesses, small
organizations, and small governmental
jurisdictions.
For purposes of assessing the impacts
of this proposed rule on small entities,
‘‘small entity’’ is defined as: (1) A small
business as defined by the Small
Business Administration’s regulations at
13 CFR 121.201; (2) a small
governmental jurisdiction that is a
government or a city, county, town,
school district or special district with a
population of less than 50,000; and (3)
a small organization that is any not-forprofit enterprise which is independently
owned and operated and is not
dominant in its field.
After considering the economic
impacts of this proposed rule on small
entities, I certify that this rule will not
have a significant economic impact on
a substantial number of small entities.
This proposed rule will not impose any
requirements on small entities. We
continue to be interested in the
potential impacts of the proposed rule
on small entities and welcome
comments on issues related to such
impacts.
D. Unfunded Mandates Reform Act
Title II of the Unfunded Mandates
Reform Act of 1995 (UMRA), Public
Law 104–4, establishes requirements for
Federal agencies to assess the effects of
their regulatory actions on State, local,
and tribal governments and the private
sector. Under section 202 of the UMRA,
we generally must prepare a written
statement, including a cost-benefit
analysis, for proposed and final rules
with ‘‘Federal mandates’’ that may
result in expenditures to State, local,
and tribal governments, in aggregate, or
to the private sector, of $100 million or
more in any 1 year. Before promulgating
an EPA rule for which a written
statement is needed, section 205 of the
UMRA generally requires us to identify
and consider a reasonable number of
regulatory alternatives and adopt the
least costly, most cost-effective, or least
burdensome alternative that achieves
the objectives of the rule. The
provisions of section 205 do not apply
when they are inconsistent with
applicable law. Moreover, section 205
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allows us to adopt an alternative other
than the least-costly, most cost-effective,
or least-burdensome alternative if the
Administrator publishes with the final
rule an explanation why that alternative
was not adopted. Before we establish
any regulatory requirements that may
significantly or uniquely affect small
governments, including tribal
governments, we must have developed
under section 203 of the UMRA a small
government agency plan. The plan must
provide for notifying potentially
affected small governments, enabling
officials of affected small governments
to have meaningful and timely input in
the development of our regulatory
proposals with significant Federal
intergovernmental mandates, and
informing, educating, and advising
small governments on compliance with
the regulatory requirements.
We have determined that this
proposed rule does not contain a
Federal mandate that may result in
expenditures of $100 million or more
for State, local, and tribal governments,
in the aggregate, or the private sector in
any one year. The proposed rule adds
only a relatively small number of new
requirements to the existing permit
requirements already in place under the
PSD program, since States are currently
implementing a PM10 surrogate program
pursuant to EPA guidance. Thus, this
proposed rulemaking is not subject to
the requirements of sections 202 and
205 of the UMRA. We have also
determined that this rule contains no
regulatory requirements that might
significantly or uniquely affect small
governments because this rule applies
only to new major stationary sources.
Thus, this proposed rulemaking is not
subject to the requirements of section
203 of the URMA.
E. Executive Order 13132: Federalism
Executive Order 13132, entitled
‘‘Federalism’’ (64 FR 43255, August 10,
1999), requires us to develop an
accountable process to ensure
‘‘meaningful and timely input by State
and local officials in the development of
regulatory policies that have federalism
implications.’’ ‘‘Policies that have
federalism implications’’ is defined in
the Executive Order to include
regulations that have ‘‘substantial direct
effects on the States, on the relationship
between the national government and
the States, or on the distribution of
power and responsibilities among the
various levels of government.’’
This proposed rule does not have
federalism implications. It would not
have substantial direct effects on the
States, on the relationship between the
national government and the States, or
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on the distribution of power and
responsibilities among the various
levels of government, as specified in
Executive Order 13132. Pursuant to the
terms of Executive Order 13132, it has
been determined that this proposed rule
does not have ‘‘federalism implications’’
because it does not meet the necessary
criteria. Thus, the requirements of
section 6 of the Executive Order do not
apply to this proposed rule.
In the spirit of Executive Order 13132,
and consistent with our policy to
promote communications between us
and State and local governments, we
specifically solicit comment on this
proposed rule from State and local
officials.
F. Executive Order 13175: Consultation
and Coordination With Indian Tribal
Governments
Executive Order 13175, entitled
‘‘Consultation and Coordination with
Indian Tribal Government’’ (65 FR
67249, November 6, 2000), requires us
to develop an accountable process to
ensure ‘‘meaningful and timely input by
tribal officials in the development of
regulatory policies that have tribal
implications.’’
This proposed rule does not have
tribal implications as defined in
Executive Order 13175. This rule
provides the elements to implement a
PM2.5 PSD program in attainment areas.
The CAA provides for States to develop
plans to regulate emissions of air
pollutants within their jurisdictions.
The Tribal Air Rule (TAR) under the
CAA gives tribes the opportunity to
develop and implement CAA programs
such as programs to attain and maintain
the PM2.5 NAAQS, but it leaves to the
discretion of the Tribe the decision of
whether to develop these programs and
which programs, or appropriate
elements of a program, they will adopt.
Although Executive Order 13175 does
not apply to this rule, EPA did reach out
to national tribal organizations in 2006
to provide a forum for tribal
professionals to provide input to the
rulemaking. However, not much
participation or input was received. It
will neither impose substantial direct
compliance costs on tribal governments,
nor preempt tribal law. The EPA
specifically solicits additional comment
on this proposed rule from tribal
officials.
G. Executive Order 13045: Protection of
Children From Environmental Health &
Safety Risks
Executive Order 13045 ‘‘Protection of
Children from Environmental Health
Risks and Safety Risks’’ (62 FR 19885,
April 23, 1997) applies to any rule that:
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54145
(1) Is determined to be ‘‘economically
significant’’ as defined under Executive
Order 12866, and (2) concerns an
environmental health or safety risk that
we have reason to believe may have a
disproportionate effect on children. If
the regulatory action meets both criteria,
the Agency must evaluate the
environmental health or safety effects of
the planned rule on children, and
explain why the planned regulation is
preferable to other potentially effective
and reasonably feasible alternatives
considered by the Agency.
This proposed rule is not subject to
the EO because it is not economically
significant as defined in EO 12866, and
because the Agency does not have a
reason to believe the environmental
health or safety risks addressed by this
action present a disproportionate risk to
children because one of the basic
requirements of the PSD program is that
new and modified major stationary
sources must demonstrate that any new
emissions do not cause or contribute to
air quality in violation of the national
ambient air quality standards. The
public is invited to submit or identify
peer-reviewed studies and data, of
which EPA may not be aware, that
assessed resolutions of early life
exposure to ambient concentrations of
fine particulate measured as PM2.5.
H. Executive Order 13211: Actions That
Significantly Affect Energy Supply,
Distribution, or Use
This rule is not a ‘‘significant energy
action’’ as defined in Executive Order
13211, ‘‘Actions Concerning Regulations
That Significantly Affect Energy Supply,
Distribution, or Use’’ (66 FR 28355 (May
22, 2001)) because it is not likely to
have a significant adverse effect on the
supply, distribution, or use of energy.
Further, we have concluded that this
rule is not likely to have any adverse
energy effects.
I. National Technology Transfer and
Advancement Act
Section 12(d) of the National
Technology Transfer and Advancement
Act of 1995 (NTTAA), Public Law No.
104–113, 12(d) (15 U.S.C. 272 note)
directs us to use voluntary consensus
standards (VCS) in our regulatory and
procurement activities unless to do so
would be inconsistent with applicable
law or otherwise impractical. The VCS
are technical standards (e.g., materials
specifications, test methods, sampling
procedures, and business practices)
developed or adopted by one or more
voluntary consensus bodies. The
NTTAA directs us to provide Congress,
through annual reports to OMB, with
explanations when we do not use
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available and applicable VCS. This
proposed rule does not involve
technical standards. Therefore, we are
not considering the use of any VCS.
J. Executive Order 12898: Federal
Actions To Address Environmental
Justice in Minority Populations and
Low-Income Populations
Executive Order 12898 (59 FR 7629
(February 16, 1994)) establishes Federal
executive policy on environmental
justice. Its main provision directs
Federal agencies, to the greatest extent
practicable and permitted by law, to
make environmental justice part of their
mission by identifying and addressing,
as appropriate, disproportionately high
and adverse human health or
environmental effects of their programs,
policies, and activities on minority
populations and low-income
populations in the United States.
The EPA has determined that this
proposed rule will not have
disproportionately high and adverse
human health environmental effects on
minority or low-income populations
because it does not affect the level of
Pollutant
protection provided to human health or
the environment. This regulation would
provide regulatory certainty for
implementing the preconstruction NSR
permitting program for PM2.5. However,
the requirements would be similar to
the existing requirements of the PM10
program and hence does not impact the
human health environmental effects.
X. Statutory Authority
Environmental protection,
Intergovernmental relations.
Dated: September 12, 2007.
Stephen L. Johnson,
Administrator.
For the reasons set out in the
preamble, title 40, chapter I of the Code
of Federal Regulations is proposed to be
amended as follows:
The statutory authority for this
proposed action is provided by sections
101, 160, 163, 165, 166, 301, and 307(d)
of the Act as amended (42 U.S.C. 7401,
7470, 7473, 7475, 7476, 7601, and
7607(d)).
PART 51—[AMENDED]
List of Subjects
Subpart I—[Amended]
40 CFR Part 51
2. Section 51.165 is amended by
revising the table in paragraph (b)(2) to
read as follows:
Administrative practices and
procedures, Air pollution control,
Environmental protection,
Intergovernmental relations.
1. The authority citation for part 51
continues to read as follows:
Authority: 23 U.S.C. 101; 42 U.S.C. 7401–
7671q.
§ 51.165
Permit requirements.
*
*
*
*
*
(b) * * *
(2) * * *
Option 1 for the table in paragraph
(b)(2):
40 CFR Part 52
Administrative practices and
procedures, Air pollution control,
Averaging time
(hours)
Annual
24
SO2 .............................
PM10 ...........................
PM2.5 ...........................
NO2 .............................
CO ..............................
1.0 µg/m3 ..................
...................................
1.0 µg/m3 ..................
1.0 µg/m3.
...................................
8
3
1
5 µg/m3 .....................
...................................
5 µg/m3.
...................................
...................................
25 µg/m3.
...................................
5 µg/m3.
...................................
0.5 mg/m3 .................
...................................
2 mg/m3.
Option 2 for the table in paragraph
(b)(2):
Pollutant
Averaging time
(hours)
Annual
24
SO2 .............................
PM10 ...........................
PM2.5 ...........................
NO2 .............................
CO ..............................
1.0 µg/m3 ..................
...................................
0.8 µg/m3 ..................
1.0 µg/m3.
...................................
8
3
5 µg/m3 .....................
5 µg/m3.
4 µg/m3.
...................................
25 µg/m3.
...................................
0.5 mg/m3 .................
...................................
1
2 mg/m3.
Option 3 for the table in paragraph
(b)(2):
Pollutant
Averaging time
(hours)
Annual
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24
SO2 .............................
PM10 ...........................
PM2.5 ...........................
NO2 .............................
CO ..............................
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1.0 µg/m3 ..................
...................................
0.3 µg/m3 ..................
1.0 µg/m3.
...................................
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8
5 µg/m3 .....................
5 µg/m3.
1.2 µg/m3.
...................................
25 µg/m3.
...................................
0.5 mg/m3 .................
...................................
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2 mg/m3.
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*
*
*
*
*
3. Section 51.166 is amended as
follows:
a. By revising the table in paragraph
(c);
b. By revising paragraph (i)(5)(i)(c);
c. By revising paragraphs (i)(5)(ii) and
(iii);
d. By revising paragraphs (i)(8) and
(9);
e. By adding paragraph (i)(10);
f. By revising paragraph (k); and
g. By revising the table in paragraph
(p)(4).
§ 51.166 Prevention of significant
deterioration of air quality.
*
*
*
*
*
(c) * * *
Option 1 for the table in paragraph (c):
Maximum allowable increase
(micrograms
per cubic
meter)
Pollutant
Class I
PM2.5:
Annual arithmetic mean ..............................................................................................................................................................
24-hr maximum ...........................................................................................................................................................................
PM10:
24-hr maximum ...........................................................................................................................................................................
Sulfur dioxide:
Annual arithmetic mean ..............................................................................................................................................................
24-hr maximum ...........................................................................................................................................................................
3-hr maximum .............................................................................................................................................................................
Nitrogen dioxide:
Annual arithmetic mean ..............................................................................................................................................................
1
3
8
2
5
25
2.5
Class II
PM2.5:
Annual arithmetic mean ..............................................................................................................................................................
24-hr maximum ...........................................................................................................................................................................
PM10:
24-hr maximum ...........................................................................................................................................................................
Sulfur dioxide:
Annual arithmetic mean ..............................................................................................................................................................
24-hr maximum ...........................................................................................................................................................................
3-hr maximum .............................................................................................................................................................................
Nitrogen dioxide:
Annual arithmetic mean ..............................................................................................................................................................
4
9
30
20
91
512
25
Class III
PM2.5:
Annual arithmetic mean ..............................................................................................................................................................
24-hr maximum ...........................................................................................................................................................................
PM10:
PM10, 24-hr maximum ................................................................................................................................................................
Sulfur dioxide:
Annual arithmetic mean ..............................................................................................................................................................
24-hr maximum ...........................................................................................................................................................................
3-hr maximum .............................................................................................................................................................................
Nitrogen dioxide:
Annual arithmetic mean ..............................................................................................................................................................
8
18
60
40
182
700
50
Option 2A for the table in paragraph
(c):
Maximum allowable increase
(micrograms
per cubic
meter)
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Pollutant
Class I
PM2.5:
Annual arithmetic mean ..............................................................................................................................................................
24-hr maximum ...........................................................................................................................................................................
PM10:
24-hr maximum ...........................................................................................................................................................................
Sulfur dioxide:
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2
8
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Maximum allowable increase
(micrograms
per cubic
meter)
Pollutant
Annual arithmetic mean ..............................................................................................................................................................
24-hr maximum ...........................................................................................................................................................................
3-hr maximum .............................................................................................................................................................................
Nitrogen dioxide:
Annual arithmetic mean ..............................................................................................................................................................
2
5
25
2.5
Class II
PM2.5:
Annual arithmetic mean ..............................................................................................................................................................
24-hr maximum ...........................................................................................................................................................................
PM10:
24-hr maximum ...........................................................................................................................................................................
Sulfur dioxide:
Annual arithmetic mean ..............................................................................................................................................................
24-hr maximum ...........................................................................................................................................................................
3-hr maximum .............................................................................................................................................................................
Nitrogen dioxide:
Annual arithmetic mean ..............................................................................................................................................................
4
9
30
20
91
512
25
Class III
PM2.5:
Annual arithmetic mean ..............................................................................................................................................................
24-hr maximum ...........................................................................................................................................................................
PM10:
24-hr maximum ...........................................................................................................................................................................
Sulfur dioxide:
Annual arithmetic mean ..............................................................................................................................................................
24-hr maximum ...........................................................................................................................................................................
3-hr maximum .............................................................................................................................................................................
Nitrogen dioxide:
Annual arithmetic mean ..............................................................................................................................................................
8
18
60
40
182
700
50
Option 2B for the table in paragraph
(c):
Maximum allowable increase
(micrograms
per cubic
meter)
Pollutant
Class I
PM2.5:
Annual arithmetic mean ................................................................................................................................................................
24-hr maximum .............................................................................................................................................................................
PM10:
24-hr maximum .............................................................................................................................................................................
Sulfur dioxide:
Annual arithmetic mean ................................................................................................................................................................
24-hr maximum .............................................................................................................................................................................
3-hr maximum ...............................................................................................................................................................................
Nitrogen dioxide:
Annual arithmetic mean ................................................................................................................................................................
1
2
8
2
5
25
2.5
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Class II
PM2.5:
Annual arithmetic mean ................................................................................................................................................................
24-hr maximum .............................................................................................................................................................................
PM10:
24-hr maximum .............................................................................................................................................................................
Sulfur dioxide:
Annual arithmetic mean ................................................................................................................................................................
24-hr maximum .............................................................................................................................................................................
3-hr maximum ...............................................................................................................................................................................
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9
30
20
91
512
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54149
Pollutant
Maximum allowable increase
(micrograms
per cubic
meter)
Nitrogen dioxide:
Annual arithmetic mean ................................................................................................................................................................
25
Class III
PM2.5:
Annual arithmetic mean ................................................................................................................................................................
24-hr maximum .............................................................................................................................................................................
PM10:
24-hr maximum .............................................................................................................................................................................
Sulfur dioxide:
Annual arithmetic mean ................................................................................................................................................................
24-hr maximum .............................................................................................................................................................................
3-hr maximum ...............................................................................................................................................................................
Nitrogen dioxide:
Annual arithmetic mean ................................................................................................................................................................
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*
*
*
*
*
(i) * * *
(5) * * *
(i) * * *
(c) Particulate matter:
(1) 10 µg/m3 of PM10, 24-hour average;
Option 1 for paragraph (i)(5)(i)(c)(2):
(2) 10 µg/m3 of PM2.5, 24-hour
average;
Option 2 for paragraph (i)(5)(i)(c):
(2) 8.0 µg/m3 of PM2.5, 24-hour
average;
Option 3 for paragraph (i)(5)(i)(c):
(2) 2.3 µg/m3 of PM2.5, 24-hour
average;
*
*
*
*
*
(ii) The concentrations of the
pollutant in the area that the source or
modification would affect are less than
the concentrations listed in paragraph
(i)(5)(i) of this section; or
(iii) The pollutant is not listed in
paragraph (i)(5)(i) of this section.
*
*
*
*
*
(8) The plan may provide that the
permitting requirements equivalent to
those contained in paragraph (k)(1)(b) of
this section do not apply to a stationary
source or modification with respect to
any maximum allowable increase for
nitrogen oxides if the owner or operator
of the source or modification submitted
an application for a permit under the
applicable permit program approved or
promulgated under the Act before the
provisions embodying the maximum
allowable increase took effect as part of
the plan and the reviewing authority
subsequently determined that the
application as submitted before that
date was complete.
(9) The plan may provide that the
permitting requirements equivalent to
those contained in paragraph (k)(1)(b ) of
this section shall not apply to a
stationary source or modification with
respect to any maximum allowable
increase for PM10 if (i) the owner or
operator of the source or modification
submitted an application for a permit
under the applicable permit program
approved under the Act before the
provisions embodying the maximum
allowable increases for PM10 took effect
as part of the plan, and (ii) the
reviewing authority subsequently
determined that the application as
submitted before that date was
complete. Instead, the applicable
requirements equivalent to paragraph
(k)(1)(b ) shall apply with respect to the
maximum allowable increases for TSP
as in effect on the date the application
was submitted.
(10) The plan may provide that the
permitting requirements equivalent to
those contained in paragraph (k)(1)(b ) of
this section shall not apply to a
stationary source or modification with
respect to any maximum allowable
increase for PM2.5 if (i) the owner or
operator of the source or modification
submitted an application for a permit
under the applicable permit program
approved under the Act before the
provisions embodying the maximum
allowable increases for PM2.5 took effect
as part of the plan, and (ii) the
reviewing authority subsequently
determined that the application as
submitted before that date was
Class I significant impact levels
Class II significant impact levels
Annual ............................................
24-hour ...........................................
0.04 µg/m3 ....................................
0.08 µg/m3 ....................................
1.0 µg/m3 ......................................
5.0 µg/m3 ......................................
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60
40
182
700
50
complete. Instead, the applicable
requirements equivalent to paragraph
(k)(1)(b ) shall apply with respect to the
maximum allowable increases for PM10
as in effect on the date the application
was submitted.
*
*
*
*
*
(k) Source impact analysis—(1)
Required demonstration. The plan 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 reduction (including
secondary emissions), would not cause
or contribute to air pollution in
violation of:
(a) Any national ambient air quality
standard in any air quality control
region; or
(b ) Any applicable maximum
allowable increase over the baseline
concentration in any area.
(2) Significant impact levels. The plan
shall provide that, for purposes of PM2.5,
the demonstration required in paragraph
(k)(1) of this section is deemed to have
been made if the emissions increase of
direct PM2.5 emissions from the new
stationary source alone or the net
emissions increase of direct PM2.5
emissions from the modification alone
would cause, in all areas, air quality
impacts less than the following
amounts:
Option 1 for the table in paragraph
(k)(2):
Averaging time
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10
18
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Class III significant impact levels
1.0 µg/m3.
5.0 µg/m3.
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Option 2 for the table in paragraph
(k)(2):
Averaging time
Class I significant impact levels
Class II significant impact levels
Annual ............................................
24-hour ...........................................
0.16 µg/m3 ....................................
0.24 µg/m3 ....................................
0.8 µg/m3 ......................................
4.0 µg/m3 ......................................
Class III significant impact levels
0.8 µg/m3.
4.0 µg/m3.
Option 3 the table in paragraph (k)(2):
Averaging time
Class I significant
impact levels
Class II significant
impact levels
Annual ............................................
24-hour ...........................................
0.06 µg/m3 ....................................
0.07 µg/m3 ....................................
0.3 µg/m3 ......................................
1.2 µg/m3 ......................................
*
*
*
(p) * * *
(4) * * *
*
*
Class III significant impact levels
0.3 µg/m3.
1.2 µg/m3.
Option 1 for the table in paragraph
(p)(4):
Maximum
allowable
increase
(micrograms
per cubic
meter)
Pollutant
PM2.5:
Annual arithmetic mean ................................................................................................................................................................
24-hr maximum .............................................................................................................................................................................
PM10:
24-hr maximum .............................................................................................................................................................................
Sulfur dioxide:
Annual arithmetic mean ................................................................................................................................................................
24-hr maximum .............................................................................................................................................................................
3-hr maximum ...............................................................................................................................................................................
Nitrogen dioxide:
Annual arithmetic mean ................................................................................................................................................................
4
9
30
20
91
325
25
Option 2A for the table in paragraph
(p)(4):
Maximum
allowable
increase
(micrograms
per cubic
meter)
Pollutant
pwalker on PROD1PC71 with PROPOSALS2
PM2.5:
Annual arithmetic mean ................................................................................................................................................................
24-hr maximum .............................................................................................................................................................................
PM10:
24-hr maximum .............................................................................................................................................................................
Sulfur dioxide:
Annual arithmetic mean ................................................................................................................................................................
24-hr maximum .............................................................................................................................................................................
3-hr maximum ...............................................................................................................................................................................
Nitrogen dioxide:
Annual arithmetic mean ................................................................................................................................................................
Option 2B for the table in paragraph
(p)(4):
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30
20
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Federal Register / Vol. 72, No. 183 / Friday, September 21, 2007 / Proposed Rules
Maximum
allowable
increase
(micrograms
per cubic
meter)
Pollutant
PM2.5:
Annual arithmetic mean ................................................................................................................................................................
24-hr maximum .............................................................................................................................................................................
PM10:
24-hr maximum .............................................................................................................................................................................
Sulfur dioxide:
Annual arithmetic mean ................................................................................................................................................................
24-hr maximum .............................................................................................................................................................................
3-hr maximum ...............................................................................................................................................................................
Nitrogen dioxide:
Annual arithmetic mean ................................................................................................................................................................
*
*
*
*
*
4. Appendix S to part 51 is amended
by revising the table in Section III.A to
read as follows:
Appendix S to Part 51—Emission Offset
Interpretative Ruling
*
*
*
*
5
9
30
20
91
325
25
A. * * *
Option 1 for the table in Section III.A:
*
III. * * *
Averaging time (hours)
Pollutant
Annual
24
SO2 .............................
PM10 ...........................
PM2.5 ...........................
NO2 .............................
CO ..............................
1.0 µg/m3 ..................
...................................
1.0 µg/m3 ..................
1.0 µg/m3. .................
...................................
8
3
1
5 µg/m3 .....................
5 µg/m3. ....................
5 µg/m3. ....................
...................................
...................................
...................................
...................................
...................................
...................................
0.5 mg/m3 .................
25 µg/m3. ..................
...................................
...................................
...................................
...................................
2 mg/m3.
Option 2 for the table in Section III.A:
Averaging time (hours)
Pollutant
Annual
24
SO2 .............................
PM10 ...........................
PM2.5 ...........................
NO2 .............................
CO ..............................
1.0 µg/m3 ..................
...................................
0.8 µg/m3 ..................
1.0 µg/m3. .................
...................................
8
3
1
5 µg/m3 .....................
5 µg/m3. ....................
4 µg/m3. ....................
...................................
...................................
...................................
...................................
...................................
...................................
0.5 mg/m3 .................
25 µg/m3. ..................
...................................
...................................
...................................
...................................
2 mg/m3.
Option 3 for the table in Section III.A:
Averaging time (hours)
Pollutant
Annual
24
8
3
...................................
...................................
...................................
...................................
0.5 mg/m3 .................
25 µg/m3. ..................
...................................
...................................
...................................
...................................
SO2 .............................
PM10 ...........................
PM2.5 ...........................
NO2 .............................
CO ..............................
1.0 µg/m3 ..................
...................................
0.3 µg/m3 ..................
1.0 µg/m3. .................
...................................
5 µg/m3 .....................
5 µg/m3. ....................
1.2 µg/m3. .................
...................................
...................................
*
** * *
Subpart A—[Amended]
*
*
*
pwalker on PROD1PC71 with PROPOSALS2
PART 52—[AMENDED]
5. The authority citation for part 52
continues to read as follows:
Authority: 42 U.S.C. 7401, et seq.
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6. Section 52.21 is amended as
follows:
a. By revising the table in paragraph
(c);
b. By revising the third entry in
paragraph (i)(5)(i);
c. By revising paragraphs (i)(5)(ii) and
(iii);
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1
2 mg/m3.
d. By revising paragraphs (i)(9) and
(10);
e. By adding paragraph (i)(11);
f. By revising paragraph (k); and
g. By revising the table in paragraph
(p)(5).
§ 52.21 Prevention of significant
deterioration of air quality.
*
*
*
(c) * * *
E:\FR\FM\21SEP2.SGM
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*
*
54152
Federal Register / Vol. 72, No. 183 / Friday, September 21, 2007 / Proposed Rules
Option 1 for the table in paragraph (c):
Maximum allowable increase
(micrograms
per cubic
meter)
Pollutant
Class I
PM2.5:
Annual arithmetic mean ..............................................................................................................................................................
24-hr maximum ...........................................................................................................................................................................
PM10:
24-hr maximum ...........................................................................................................................................................................
Sulfur dioxide:
Annual arithmetic mean ..............................................................................................................................................................
24-hr maximum ...........................................................................................................................................................................
3-hr maximum .............................................................................................................................................................................
Nitrogen dioxide:
Annual arithmetic mean ..............................................................................................................................................................
1
2
8
2
5
25
2.5
Class II
PM2.5:
Annual arithmetic mean ..............................................................................................................................................................
24-hr maximum ...........................................................................................................................................................................
PM10:
24-hr maximum ...........................................................................................................................................................................
Sulfur dioxide:
Annual arithmetic mean ..............................................................................................................................................................
24-hr maximum ...........................................................................................................................................................................
3-hr maximum .............................................................................................................................................................................
Nitrogen dioxide:
Annual arithmetic mean ..............................................................................................................................................................
4
9
30
20
91
512
25
Class III
PM2.5:
Annual arithmetic mean ..............................................................................................................................................................
24-hr maximum ...........................................................................................................................................................................
PM10:
PM10 24-hr maximum .................................................................................................................................................................
Sulfur dioxide:
Annual arithmetic mean ..............................................................................................................................................................
24-hr maximum ...........................................................................................................................................................................
3-hr maximum .............................................................................................................................................................................
Nitrogen dioxide:
Annual arithmetic mean ..............................................................................................................................................................
8
18
60
40
182
700
50
Option 2A for the table in paragraph
(c):
Maximum
allowable
increase
(micrograms
per cubic
meter)
Pollutant
pwalker on PROD1PC71 with PROPOSALS2
Class I
PM2.5:
Annual arithmetic mean ..............................................................................................................................................................
24-hr maximum ...........................................................................................................................................................................
PM10:
24-hr maximum ...........................................................................................................................................................................
Sulfur dioxide:
Annual arithmetic mean ..............................................................................................................................................................
24-hr maximum ...........................................................................................................................................................................
3-hr maximum .............................................................................................................................................................................
Nitrogen dioxide:
Annual arithmetic mean ..............................................................................................................................................................
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2
8
2
5
25
2.5
Federal Register / Vol. 72, No. 183 / Friday, September 21, 2007 / Proposed Rules
54153
Maximum
allowable
increase
(micrograms
per cubic
meter)
Pollutant
Class II
PM2.5:
Annual arithmetic mean ..............................................................................................................................................................
24-hr maximum ...........................................................................................................................................................................
PM10:
24-hr maximum ...........................................................................................................................................................................
Sulfur dioxide:
Annual arithmetic mean ..............................................................................................................................................................
24-hr maximum ...........................................................................................................................................................................
3-hr maximum .............................................................................................................................................................................
Nitrogen dioxide:
Annual arithmetic mean ..............................................................................................................................................................
4
9
30
20
91
512
25
Class III
PM2.5:
Annual arithmetic mean ..............................................................................................................................................................
24-hr maximum ...........................................................................................................................................................................
PM10:
24-hr maximum ...........................................................................................................................................................................
Sulfur dioxide:
Annual arithmetic mean ..............................................................................................................................................................
24-hr maximum ...........................................................................................................................................................................
3-hr maximum .............................................................................................................................................................................
Nitrogen dioxide:
Annual arithmetic mean ..............................................................................................................................................................
8
18
60
40
182
700
50
Option 2B for the table in paragraph
(c):
Maximum
allowable
increase
(micrograms
per cubic
meter)
Pollutant
Class I
PM2.5:
Annual arithmetic mean ..............................................................................................................................................................
24-hr maximum ...........................................................................................................................................................................
PM10:
24-hr maximum ...........................................................................................................................................................................
Sulfur dioxide:
Annual arithmetic mean ..............................................................................................................................................................
24-hr maximum ...........................................................................................................................................................................
3-hr maximum .............................................................................................................................................................................
Nitrogen dioxide:
Annual arithmetic mean ..............................................................................................................................................................
1
2
8
2
5
25
2.5
pwalker on PROD1PC71 with PROPOSALS2
Class II
PM2.5:
Annual arithmetic mean ..............................................................................................................................................................
24-hr maximum ...........................................................................................................................................................................
PM10:
24-hr maximum ...........................................................................................................................................................................
Sulfur dioxide:
Annual arithmetic mean ..............................................................................................................................................................
24-hr maximum ...........................................................................................................................................................................
3-hr maximum .............................................................................................................................................................................
Nitrogen dioxide:
Annual arithmetic mean ..............................................................................................................................................................
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Federal Register / Vol. 72, No. 183 / Friday, September 21, 2007 / Proposed Rules
Maximum
allowable
increase
(micrograms
per cubic
meter)
Pollutant
Class III
PM2.5:
Annual arithmetic mean ..............................................................................................................................................................
24-hr maximum ...........................................................................................................................................................................
PM10:
24-hr maximum ...........................................................................................................................................................................
Sulfur dioxide:
Annual arithmetic mean ..............................................................................................................................................................
24-hr maximum ...........................................................................................................................................................................
3-hr maximum .............................................................................................................................................................................
Nitrogen dioxide:
Annual arithmetic mean ..............................................................................................................................................................
*
*
*
*
*
(i) * * *
(5) * * *
(i) * * *
Option 1 for the third entry in
paragraph (i)(5)(i):
Particulate matter:
(a) 10 µg/m3 of PM10, 24-hour average;
(b) 10 µg/m3 of PM2.5, 24-hour
average;
Option 2 for the third entry in
paragraph (i)(5):
Particulate matter:
(a) 10 µg/m3 of PM10, 24-hour average;
(b) 8.0 µg/m3 of PM2.5, 24-hour
average;
Option 3 for the third entry in
paragraph (i)(5):
Particulate matter:
(a) 10 µg/m3 of PM10, 24-hour average;
(b) 2.3 µg/m3 of PM2.5, 24-hour
average;
*
*
*
*
*
(ii) The concentrations of the
pollutant in the area that the source or
modification would affect are less than
the concentrations listed in paragraph
(i)(5)(i) of this section; or
(iii) The pollutant is not listed in
paragraph (i)(5)(i) of this section.
*
*
*
*
*
(9) The requirements of paragraph
(k)(1)(a) of this section shall not apply
to a stationary source or modification
with respect to any maximum allowable
increase for nitrogen oxides if the owner
or operator of the source or modification
submitted an application for a permit
under this section before the provisions
pwalker on PROD1PC71 with PROPOSALS2
Averaging time
embodying the maximum allowable
increase took effect as part of the
applicable implementation plan and the
Administrator subsequently determined
that the application as submitted before
that date was complete.
(10) The requirements in paragraph
(k)(1)(b) of this section shall not apply
to a stationary source or modification
with respect to any maximum allowable
increase for PM10 if (i) the owner or
operator of the source or modification
submitted an application for a permit
under this section before the provisions
embodying the maximum allowable
increases for PM10 took effect in an
implementation plan to which this
section applies, and (ii) the
Administrator subsequently determined
that the application as submitted before
that date was otherwise complete.
Instead, the requirements in paragraph
(k)(1)(b) shall apply with respect to the
maximum allowable increases for TSP
as in effect on the date the application
was submitted.
(11) The requirements in paragraph
(k)(1)(b) of this section shall not apply
to a stationary source or modification
with respect to any maximum allowable
increase for PM2.5 if (i) the owner or
operator of the source or modification
submitted an application for a permit
under this section before the provisions
embodying the maximum allowable
increases for PM2.5 took effect in an
implementation plan to which this
section applies, and (ii) the
Administrator subsequently determined
Class I significant impact levels
Annual ............................................
24-hour ...........................................
µg/m3
0.04
....................................
0.08 µg/m3 ....................................
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Class II significant impact levels
µg/m3
1.0
......................................
5.0 µg/m3 ......................................
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60
40
182
700
50
that the application as submitted before
that date was otherwise complete.
Instead, the requirements in paragraph
(k)(1)(b) shall apply with respect to the
maximum allowable increases for PM10
as in effect on the date the application
was submitted.
*
*
*
*
*
(k) Source impact analysis—(1)
Required demonstration. 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:
(a) Any national ambient air quality
standard in any air quality control
region; or
(b) Any applicable maximum
allowable increase over the baseline
concentration in any area.
(2) Significant impact levels. For
purposes of PM2.5, the demonstration
required in paragraph (k)(1) of this
section is deemed to have been made if
the emissions increase of direct PM2.5
emissions from the new stationary
source alone or the net emissions
increase of direct PM2.5 emissions from
the modification alone would cause, in
all areas, air quality impacts less than
the following amounts:
Option 1 for the table in paragraph
(k)(2):
Class III significant impact levels
1.0 µg/m3.
5.0 µg/m3.
Option 2 for the table in paragraph
(k)(2):
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Averaging time
Class I significant impact levels
Class II significant impact levels
Annual ............................................
24-hour ...........................................
0.16 µg/m3 ....................................
0.24 µg/m3 ....................................
0.8 µg/m3 ......................................
4.0 µg/m3 ......................................
54155
Class III significant impact levels
0.8 µg/m3.
4.0 µg/m3.
Option 3 for the table in paragraph
(k)(2):
Averaging time
Class I significant impact levels
Class II significant impact levels
Annual ............................................
24-hour ...........................................
0.06 µg/m3 ....................................
0.07 µg/m3 ....................................
0.3 µg/m3 ......................................
1.2 µg/m3 ......................................
*
*
*
(p) * * *
(5) * * *
*
*
Class III significant impact levels
0.3 µg/m3.
1.2 µg/m3.
Option 1 for the table in paragraph
(p)(5):
Maximum allowable increase
(micrograms
per cubic
meter)
Pollutant
PM2.5:
Annual arithmetic mean ................................................................................................................................................................
24-hr maximum .............................................................................................................................................................................
PM10:
24-hr maximum .............................................................................................................................................................................
Sulfur dioxide:
Annual arithmetic mean ................................................................................................................................................................
24-hr maximum .............................................................................................................................................................................
3-hr maximum ...............................................................................................................................................................................
Nitrogen dioxide:
Annual arithmetic mean ................................................................................................................................................................
4
9
30
20
91
325
25
Option 2 for the table in paragraph
(p)(5):
Maximum allowable increase
(micrograms
per cubic
meter)
Pollutant
PM2.5:
Annual arithmetic mean ................................................................................................................................................................
24-hr maximum .............................................................................................................................................................................
PM10:
24-hr maximum .............................................................................................................................................................................
Sulfur dioxide:
Annual arithmetic mean ................................................................................................................................................................
24-hr maximum .............................................................................................................................................................................
3-hr maximum ...............................................................................................................................................................................
Nitrogen dioxide:
Annual arithmetic mean ................................................................................................................................................................
4
9
30
20
91
325
25
pwalker on PROD1PC71 with PROPOSALS2
Option 3 for the table in paragraph
(p)(5):
Maximum allowable increase
(micrograms
per cubic
meter)
Pollutant
PM2.5:
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Federal Register / Vol. 72, No. 183 / Friday, September 21, 2007 / Proposed Rules
Maximum allowable increase
(micrograms
per cubic
meter)
Pollutant
Annual arithmetic mean ................................................................................................................................................................
24-hr maximum .............................................................................................................................................................................
PM10:
24-hr maximum .............................................................................................................................................................................
Sulfur dioxide:
Annual arithmetic mean ................................................................................................................................................................
24-hr maximum .............................................................................................................................................................................
3-hr maximum ...............................................................................................................................................................................
Nitrogen dioxide:
Annual arithmetic mean ................................................................................................................................................................
*
*
*
*
*
[FR Doc. E7–18346 Filed 9–20–07; 8:45 am]
pwalker on PROD1PC71 with PROPOSALS2
BILLING CODE 6560–50–P
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9
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Agencies
[Federal Register Volume 72, Number 183 (Friday, September 21, 2007)]
[Proposed Rules]
[Pages 54112-54156]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E7-18346]
[[Page 54111]]
-----------------------------------------------------------------------
Part II
Environmental Protection Agency
-----------------------------------------------------------------------
40 CFR Parts 51 and 52
Prevention of Significant Deterioration (PSD) for Particulate Matter
Less Than 2.5 Micrometers (PM2.5)--Increments, Significant
Impact Levels (SILs) and Significant Monitoring Concentration (SMC);
Proposed Rule
Federal Register / Vol. 72, No. 183 / Friday, September 21, 2007 /
Proposed Rules
[[Page 54112]]
-----------------------------------------------------------------------
ENVIRONMENTAL PROTECTION AGENCY
40 CFR Parts 51 and 52
[EPA-HQ-OAR-2006-0605; FRL-8470-1]
RIN 2060-AO24
Prevention of Significant Deterioration (PSD) for Particulate
Matter Less Than 2.5 Micrometers (PM2.5)--Increments,
Significant Impact Levels (SILs) and Significant Monitoring
Concentration (SMC)
AGENCY: Environmental Protection Agency (EPA).
ACTION: Proposed rule.
-----------------------------------------------------------------------
SUMMARY: The Clean Air Act (Act) authorizes EPA to establish
regulations to prevent significant deterioration of air quality due to
emissions of any pollutant for which a national ambient air quality
standard (NAAQS) has been promulgated. The NAAQS for particulate matter
using the PM2.5 indicator were promulgated in 1997. The EPA
is proposing to facilitate implementation of a PM2.5
Prevention of Significant Deterioration (PSD) program in areas
attaining the particulate matter less than 2.5 micrometers
(PM2.5) NAAQS by developing PM2.5 increments,
Significant Impact Levels (SILs), and a Significant Monitoring
Concentration (SMC). In addition, EPA is proposing to revoke the annual
PM10 increments.
``Increments'' are maximum increases in ambient PM2.5
concentrations (PM2.5 increments) allowed in an area above
the baseline concentration. The SILs and SMCs are numerical values that
represent thresholds of insignificant, i.e., de minimis, modeled source
impacts or monitored (ambient) concentrations, respectively. The EPA is
proposing such values for PM2.5 that will be used as
screening tools by a major source subject to PSD to determine the
subsequent level of analysis and data gathering required for a PSD
permit application for emissions of PM2.5.
DATES: Comments must be received on or before November 20, 2007. Under
the Paperwork Reduction Act, comments on the information collection
provisions must be received by the Office of Management and Budget
(OMB) on or before October 22, 2007.
Public Hearing. If anyone contacts us requesting to speak at a
public hearing by October 11, 2007, we will hold a public hearing.
Additional information about the hearing would be published in a
subsequent Federal Register notice.
ADDRESSES: Submit your comments, identified by Docket ID No. EPA-HQ-
OAR-2006-0605, by one of the following methods:
www.regulations.gov. Follow the on-line instructions for
submitting comments.
E-mail: a-and-r-Docket@.epa.gov.
Mail: Air and Radiation Docket and Information Center,
Environmental Protection Agency, Mailcode: 2822T, 1200 Pennsylvania
Avenue, NW., Washington, DC 20460. Please include a total of two
copies. In addition, please mail a copy of your comments on the
information collection provisions to the Office of Information and
Regulatory Affairs, Office of Management and Budget (OMB), Attn: Desk
Officer for EPA, 725 17th Street, Northwest, Washington, DC 20503.
Hand Delivery: Air and Radiation Docket and Information
Center, EPA/DC, EPA West, Room 3334, 1301 Constitution Avenue, NW.,
Washington, DC 20004. Such deliveries are only accepted during the
Docket Center's normal hours of operation, and special arrangements
should be made for deliveries of boxed information.
Instructions: Direct your comments to Docket ID No. EPA-HQ-OAR-
2006-0605. The EPA's policy is that all comments received will be
included in the public docket without change and may be made available
online at www.regulations.gov, including any personal information
provided, unless the comment includes information claimed to be
Confidential Business Information (CBI) or other information whose
disclosure is restricted by statute. Do not submit information that you
consider to be CBI or otherwise protected through www.regulations.gov
or e-mail. The www.regulations.gov Web site is an ``anonymous access''
system, which means EPA will not know your identity or contact
information unless you provide it in the body of your comment. If you
send an e-mail comment directly to EPA without going through
www.regulations.gov your e-mail address will be automatically captured
and included as part of the comment that is placed in the public docket
and made available on the Internet. If you submit an electronic
comment, EPA recommends that you include your name and other contact
information in the body of your comment and with any disk or CD-ROM you
submit. If EPA cannot read your comment due to technical difficulties
and cannot contact you for clarification, EPA may not be able to
consider your comment. Electronic files should avoid the use of special
characters, any form of encryption, and be free of any defects or
viruses. For additional instructions on submitting comments, go to
section I.B of the SUPPLEMENTARY INFORMATION section of this document.
Docket: All documents in the docket are listed in the
www.regulations.gov index. 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, will be publicly available only in hard copy.
Publicly available docket materials are available either electronically
in www.regulations.gov or in hard copy at the Air and Radiation Docket
and Information Center, EPA/DC, EPA West, Room 3334, 1301 Constitution
Avenue, Northwest, Washington, DC. The Public Reading Room is open from
8:30 a.m. to 4:30 p.m., Monday through Friday, excluding legal
holidays. The telephone number for the Public Reading Room is (202)
566-1744, and the telephone number for the Air and Radiation Docket and
Information Center is (202) 566-1742.
FOR FURTHER INFORMATION CONTACT: Mr. Raghavendra (Raj) Rao, Air Quality
Policy Division, Office of Air Quality Planning and Standards (C504-
03), Environmental Protection Agency, Research Triangle Park, North
Carolina 27711; telephone number (919) 541-5344; fax number (919) 541-
5509; e-mail address: rao.raj@epa.gov or Dan deRoeck, Air Quality
Policy Division, Office of Air Quality Planning and Standards (C504-
03), Environmental Protection Agency, Research Triangle Park, North
Carolina 27711; telephone number (919) 541-5593; fax number (919) 541-
5509; e-mail address: deroeck.dan@epa.gov. To request a public hearing
or information pertaining to a public hearing on this document, contact
Ms. Pamela S. Long, Air Quality Policy Division, Office of Air Quality
Planning and Standards (C504-03), Environmental Protection Agency,
Research Triangle Park, North Carolina 27711; telephone number (919)
541-0641; fax number (919) 541-5509; e-mail address: long.pam@epa.gov.
SUPPLEMENTARY INFORMATION:
I. General Information
A. Does this action apply to me?
Entities potentially affected by this proposed action include
owners and operators of emission sources in all industry groups, as
well as the EPA and State, local, and tribal governments that are
delegated authority to implement these regulations. The majority of
sources potentially affected are expected to be in the following
groups:
[[Page 54113]]
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Category NAICS\a\ Industry group
----------------------------------------------------------------------------------------------------------------
Industry......................... 221111, 221112, Electric services.
221113, 221119,
221121, 221122.
32411............... Petroleum refining.
325181, 32512, Industrial inorganic chemicals.
325131, 325182,
211112, 325998,
331311, 325188.
32511, 325132, Industrial organic chemicals.
325192, 325188,
325193, 32512,
325199.
32552, 32592, 32591, Miscellaneous chemical products.
325182, 32551.
211112.............. Natural gas liquids.
48621, 22121........ Natural gas transport.
32211, 322121, Pulp and paper mills.
322122, 32213.
322121, 322122...... Paper mills.
336111, 336112, Automobile manufacturing.
336712, 336211,
336992, 336322,
336312, 33633,
33634, 33635,
336399, 336212,
336213.
325411, 325412, Pharmaceuticals.
325413, 325414.
Federal government............... 924110.............. Administration of Air and Water Resources and Solid
Waste Management Programs.
State/local/tribal Government.... 924110.............. Administration of Air and Water Resources and Solid
Waste Management Programs.
----------------------------------------------------------------------------------------------------------------
\a\ North American Industry Classification System.
This table is not intended to be exhaustive, but rather provides a
guide for readers regarding entities likely to be regulated by this
action. To determine whether your facility is regulated by this action,
you should examine the applicability criteria in the PSD rules for
attainment areas (40 CFR 52.21). If you have any questions regarding
the applicability of this action to a particular entity, contact the
person listed in the preceding FOR FURTHER INFORMATION CONTACT section.
B. What should I consider as I prepare my comments for EPA?
1. Submitting CBI. Do not submit this information to EPA through
www.regulations.gov or e-mail. Clearly mark the part or all of the
information that you claim to be CBI. For CBI information in a disk or
CD ROM that you mail to EPA, mark the outside of the disk or CD ROM as
CBI and then identify electronically within the disk or CD ROM the
specific information that is claimed as CBI. In addition to one
complete version of the comment that includes information claimed as
CBI, a copy of the comment that does not contain the information
claimed as CBI must be submitted for inclusion in the public docket.
Information so marked will not be disclosed except in accordance with
procedures set forth in 40 CFR part 2. Send or deliver information
identified as CBI only to the following address: Roberto Morales, OAQPS
Document Control Officer (C404-02), Environmental Protection Agency,
Research Triangle Park, NC 27711, Attention Docket ID No. EPA-HQ-OAR-
2006-0605.
2. Tips for Preparing Your Comments. When submitting comments,
remember to:
Identify the rulemaking by docket number and other
identifying information (subject heading, Federal Register date and
page number).
Follow directions--The agency may ask you to respond to
specific questions or organize comments by referencing a Code of
Federal Regulations (CFR) part or section 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.
If you estimate potential costs or burdens, explain how
you arrived at your estimate in sufficient detail to allow for it to be
reproduced.
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.
C. Where can I get a copy of this document and other related
information?
In addition to being available in the docket, an electronic copy of
this proposal will also be available on the World Wide Web. Following
signature by the EPA Administrator, a copy of this notice will be
posted in the regulations and standards section of our NSR home page
located at https://www.epa.gov/nsr.
D. How can I find information about a possible Public Hearing?
Persons interested in presenting oral testimony should contact Ms.
Pamela Long, New Source Review Group, Air Quality Policy Division
(C504-03), Environmental Protection Agency, Research Triangle Park, NC
27711; telephone number (919) 541-0641 or e-mail long.pam@epa.gov at
least 2 days in advance of the public hearing. Persons interested in
attending the public hearing should also contact Ms. Long to verify the
time, date, and location of the hearing. The public hearing will
provide interested parties the opportunity to present data, views, or
arguments concerning these proposed rules.
The information presented in this preamble is organized as follows:
I. General Information
A. Does this action apply to me?
B. What should I consider as I prepare my comments for EPA?
C. Where can I get a copy of this document and other related
information?
D. How can I find information about a possible Public Hearing?
II. Overview of Proposed Regulations
A. Summary of Proposed Options for Increments
B. Summary of Proposed Options for SILs
C. Summary of Proposed Options for the PM2.5 SMC
III. Background
A. PSD Program
B. History of PM NAAQS
1. TSP and PM10 NAAQS
2. PM2.5 NAAQS
3. Revised PM2.5 and PM10 NAAQS
C. Implementation of NSR for PM2.5
D. Background on Implementation of PSD Increments
[[Page 54114]]
E. Historical Approaches for Developing Increments
1. Congressional Enactment of Increments for PM and
SO2.
2. EPA's promulgation of increments for NO2 and
PM10
a. Increments for NOX Using the ``Contingent Safe
Harbor'' Approach Under Section 166(a) of the Act
b. Increments for PM10 Using ``Equivalent
Substitution'' Approach Under Section 166(f)
IV. EPA's Interpretation of Section 166 of the Clean Air Act
A. Which Criteria In Section 166 Should EPA Use to Develop
Increments for PM2.5?
1. Support for ``Contingent Safe Harbor'' Approach for
PM2.5 Under Section 166(a)
2. Support of ``Equivalent Substitution'' Approach for
PM2.5 Under Section 166(f)
B. Requirements of Sections 166(a)-(d) of the Clean Air Act
1. Regulations as a Whole Should Fulfill Statutory Requirements
2. Contingent Safe Harbor Approach
3. The Statutory Factors Applicable Under Section 166(c)
4. Balancing the Factors Applicable Under Section 166(c)
5. Authority for States to Adopt Alternatives to Increments
C. Requirements of Section 166(f) of the Clean Air Act
V. Increments and Other Measures to Prevent Significant
Deterioration
A. Option 1--Contingent Safe Harbor Approach for Annual and
Short-Term Increments--Section 166(a)
1. Proposed Framework for Pollutant Specific PSD Regulations for
PM2.5
a. Increment System
b. Area Classifications
c. Permitting Procedures
d. Air Quality Related Values Review by Federal Land Manager and
Reviewing Authority
e. Additional Impacts Analysis
f. Installation of Best Available Control Technology
2. Proposed Increments
a. Identification of Safe Harbor Increments
b. Data Utilized by EPA for the Evaluation of the Safe Harbor
Increments for PM2.5
c. Scope of Effects Considered
d. Evaluation of the Health and Welfare Effects of
PM2.5
e. Fundamental Elements of Increments
f. Evaluation of the Safe Harbor Increments
3. Proposed Baseline Dates for PM2.5 Increments Under
Option 1
4. Revocation of PM10 Annual Increments
B. Option 2--Equivalent Substitution Approach for Annual
Increments--Section 166(f)
1. Development of Equivalent Increments
2. Proposed Annual Increments for PM2.5
a. Option 2A
b. Option 2B
3. Baseline dates
VI. Significant Impact Levels (SILs)
A. EPA's Guidance on SILs in the PSD Program
B. Legal Basis for SILs
C. Relationship of SILs to AQRVs
D. Proposed Options for PM2.5 SILs (for PSD and NA-
NSR)
1. Option 1. Propose SILs using the approach we proposed for
PM10 in 1996
2. Option 2. PM2.5 to PM10 Emissions Ratio
3. Option 3. PM2.5 to PM10 NAAQS Ratio
VII. Significant Monitoring Concentrations (SMCs)
A. Background on SMCs
1. Preconstruction Monitoring and Its Role in NSR Program
2. History of SMC Rules Adopted by EPA
B. Legal Basis for SMCs
C. Proposed Options for PM2.5 SMC
1. Option 1. Lowest Detectable Concentration
2. Option 2. PM2.5 to PM10 Emissions Ratio
3. Option 3. PM2.5 to PM10 NAAQS Ratio
D. Correction of Cross References
VIII. Effective Date of the Final Rule, SIP Submittal/Approval
Deadlines and PM10 Revocation Deadline
A. Option 1: Increments promulgated pursuant to section 166(a)
of the Act.
1. Effective Date of Final Rule
2. State Program
3. Federal Program
B. Option 2: Increments Promulgated Pursuant to Section 166(f)
of the Act.
1. Effective date of Final Rule
2. State Program
3. Federal Program
C. Revocation of the PM10 Increment
D. Transition Period
E. Effective Date for SILs and SMCs
IX. Statutory and Executive Order Reviews
A. Executive Order 12866: Regulatory Planning and Review
B. Paperwork Reduction Act
C. Regulatory Flexibility Act
D. Unfunded Mandates Reform Act
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 & Safety Risks
H. Executive Order 13211: Actions That Significantly Affect
Energy Supply, Distribution, or Use
I. National Technology Transfer and Advancement Act
J. Executive Order 12898: Federal Actions to Address
Environmental Justice in Minority Populations and Low-Income
Populations
X. Statutory Authority
II. Overview of Proposed Regulations
This proposal is the first step in the rulemaking process for
promulgating PM2.5 increments, SILs, and a SMC. The purpose
of this proposed rulemaking is to develop the final elements that will
aid implementation of the PSD program for PM2.5. When final,
these elements will supplement the final NSR implementation rule for
PM2.5. Following final action on this proposal and the
PM2.5 implementation rule for NSR, the Federal
PM2.5 NSR programs will no longer have to rely on the
PM10 program as a surrogate, as has been the practice under
our existing guidance. A State implementing a NSR program in an EPA
approved State Implementation Plan (SIP) may continue to rely on the
interim surrogate policy until we approve a revised SIP addressing
these requirements. In this rulemaking, we \1\ are proposing several
options for increments, SILs and the SMC, respectively.
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\1\ In this proposal, the terms ``we,'' ``us,'' and ``our''
refer to the EPA and the terms ``you'' and ``your'' refer to the
owners or operators of stationary sources of air pollution.
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A. Summary of Proposed Options for Increments
We are proposing three sets of PM2.5 increments, based
on several approaches that are described in greater detail later in
this preamble. For the first set (option 1), we are relying on an
approach that treats PM2.5 as a new pollutant. This option
follows our statutory authority section 166(a) of the Act to develop
increments for ``pollutants for which national ambient air quality
standards are promulgated after the date of enactment of this part * *
* '' This is the same approach that we used to establish NOX
increment regulations on October 12, 2005 (70 FR at 59586). The second
and third options (options 2A and 2B) rely on an approach that we used
in 1993 to promulgate PM10 increments in lieu of the
statutory increments for particulate matter (PM) following our
replacement of the then existing indicator for the PM NAAQS based on
total suspended particulate with a new indicator based on
PM10. (58 FR 31622, June 3, 1993.) These two options
represent variations of the approach used under the authority of
section 166(f) of the Act to ``substitute'' PM10 increments
for TSP increments. The increment values resulting from each of these
three options are:
[[Page 54115]]
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Proposed increments ([mu]g/m\3\) NAAQS ([mu]g/m\3\)
---------------------------------------------------------------------------------------
Option Class I Class II Class III
------------------------------------------------------------------ Annual 24-hr
Annual 24-hr Annual 24-hr Annual 24-hr
--------------------------------------------------------------------------------------------------------------------------------------------------------
1............................................................... 1 2 4 9 8 18 ......... .........
2A.............................................................. 1 2 4 9 8 18 15 35
2B.............................................................. 1 2 5 9 10 18 ......... .........
--------------------------------------------------------------------------------------------------------------------------------------------------------
B. Summary of Proposed Options for SILs
We are also proposing three options for SILs. The first option
utilizes the same approach we proposed for PM10 in the 1996
NSR Reform proposal. For option 2, we are proposing to scale the
PM10 SIL values by the ratio of direct PM2.5 to
direct PM10 emissions. The PM2.5/PM10
emissions ratio is the national average derived from the 2001
extrapolation of the 1999 National Emissions Inventory. For option 3,
we are proposing to scale the PM10 SIL values by the ratio
of the PM2.5 NAAQS to the PM10 NAAQS. The SIL
values resulting from each of these options are:
----------------------------------------------------------------------------------------------------------------
Proposed SILs ([mu]g/m\3\)
-----------------------------------------------------------------
Option Class I Class II Class III
-----------------------------------------------------------------
Annual 24-hr Annual 24-hr Annual 24-hr
----------------------------------------------------------------------------------------------------------------
1............................................. 0.04 0.08 1.0 5.0 1.0 5.0
2............................................. 0.16 0.24 0.8 4.0 0.8 4.0
3............................................. 0.06 0.07 0.3 1.2 0.3 1.2
----------------------------------------------------------------------------------------------------------------
C. Summary of Proposed Options for the PM2.5 SMC
The first option we are proposing for the SMC is the ``Lowest
Detection Concentration'' or LDC approach that we used for establishing
the SMC for TSP and PM10. For option 2, we are proposing to
scale the PM10 SMC value by the ratio of direct
PM2.5 to direct PM10 emissions. The
PM2.5/PM10 emissions ratio is the national
average derived from the 2001 extrapolation of the 1999 National
Emissions Inventory. For option 3, we are proposing to scale the
PM10 SMC value by the ratio of the PM2.5 NAAQS to
the PM10 NAAQS. The proposed SMC values for each of these
options for the 24-hour averaging period are:
Option 1--10 [mu]g/m\3\
Option 2--7.9 [mu]g/m\3\
Option 3--2.3 [mu]g/m\3\
III. Background
A. PSD Program
The NSR provisions of the Act are a combination of air quality
planning and air pollution control technology program requirements for
new and modified stationary sources of air pollution. In brief, section
109 of the Act requires us to promulgate primary NAAQS to protect
public health and secondary NAAQS to protect public welfare. Once we
have set these standards, States must develop, adopt, and submit to us
for approval SIPs that contain emission limitations and other control
measures to attain and maintain the NAAQS and to meet the other
requirements of section 110(a) of the Act. Part C of title I of the Act
contains the requirements for a component of the major new source
review (NSR) program known as the PSD program. This program sets forth
procedures for the preconstruction review and permitting of new and
modified major stationary sources of air pollution locating in areas
meeting the NAAQS (``attainment'' areas) and areas for which there is
insufficient information to classify an area as either attainment or
nonattainment (``unclassifiable'' areas). Most states have SIP-approved
preconstruction permit (major NSR) programs. The Federal PSD program at
40 CFR 52.21 applies in some States that lack a SIP-approved permit
program, and in Indian country.\2\ The applicability of the PSD program
to a major stationary source must be determined in advance of
construction and is a pollutant specific determination. Once a major
source is determined to be subject to the PSD program (PSD source),
among other requirements, it must undertake a series of analyses to
demonstrate that it will use the best available control technology
(BACT) and will not cause or contribute to a violation of any NAAQS or
incremental ambient pollutant concentration increase (increment). In
cases where the source's emissions may adversely affect an area
classified as a Class I area, additional review is conducted to protect
the increments and special attributes of such an area defined as ``air
quality related values.''
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\2\ We have delegated authority to some States to implement the
Federal PSD program. The EPA remains the reviewing authority in non-
delegated States and in Indian country.
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As part of the analysis of air quality impacts to determine
compliance with the NAAQS and increment, the permit applicant and
reviewing authority may compare the source's impacts for a pollutant
with the corresponding SIL for that pollutant to show that a cumulative
air quality impacts analysis is not necessary. Similarly, the permit
applicant and reviewing authority may use the corresponding SMC for
that pollutant to determine if pre-application site-specific ambient
monitoring data is needed to conduct the air quality analysis.
When the reviewing authority reaches a preliminary decision to
authorize construction of each proposed major new source or major
modification, it must provide notice of the preliminary decision and an
opportunity for comment by the general public, industry, and other
persons that may be affected by the emissions of the major source or
major modification. After considering these comments, the reviewing
authority may issue a final determination on the construction permit in
accordance with the PSD regulations.
[[Page 54116]]
B. History of PM NAAQS
1. TSP and PM10 NAAQS
The EPA initially established NAAQS for PM in 1971, measured by the
TSP indicator. Based on the size of the particles collected by the
``high-volume sampler,'' which was the reference method for determining
ambient concentrations, TSP included all PM up to a nominal size of 25
to 45 micrometers. We established both annual and 24-hour NAAQS for
TSP.
On July 1, 1987, we promulgated new NAAQS for PM in which we
changed the indicator from TSP to PM10, the latter including
particles with a mean aerodynamic diameter less than or equal to 10
micrometers. These smaller particles are the subset of inhalable
particles small enough to penetrate to the thoracic region (including
the tracheobronchial and alveolar regions) of the respiratory tract
(referred to as thoracic particles). We established annual and 24-hour
NAAQS for PM10, and revoked the NAAQS for TSP. (52 FR
24634).
2. PM2.5 NAAQS
On July 18, 1997, we again revised the NAAQS for PM in several
respects. While we determined that the NAAQS should continue to focus
on particles less than or equal to 10 micrometers in diameter, we also
determined that the fine and coarse fractions of PM10 should
be considered separately. We established new annual and 24-hour NAAQS
for PM2.5 (referring to particles with a nominal mean
aerodynamic diameter less than or equal to 2.5 micrometers) as the
indicator for fine particles. Our 1997 rules also modified the
PM10 NAAQS for the purpose of regulating the coarse fraction
of PM10 (referred to as thoracic coarse particles or coarse-
fraction particles; generally including particles with a nominal mean
aerodynamic diameter greater than 2.5 micrometers and less than or
equal to 10 micrometers, or PM10-2.5), however
this part of the action was vacated during subsequent litigation,
leaving the pre-existing 1987 PM10 NAAQS in place (62 FR
38652).
3. Revised PM2.5 and PM10 NAAQS
On October 17, 2006, we promulgated revisions to the NAAQS for
PM2.5 and PM10 with an effective date of December
18, 2006 (71 FR 61144). We lowered the 24-hour NAAQS for
PM2.5 from 65 micrograms per cubic meter ([mu]g/m\3\) to 35
[mu]g/m\3\, and retained the existing annual PM2.5 NAAQS of
15 [mu]g/m\3\. In addition, we retained the existing PM10
24-hour NAAQS of 150 [mu]g/m\3\, and revoked the annual PM10
NAAQS (previously set at 50 [mu]g/m\3\).
C. Implementation of NSR for PM2.5
After we established new annual and 24-hour NAAQS for
PM2.5 (referring to particles with a nominal mean
aerodynamic diameter less than or equal to 2.5 micrometers) as the
indicator for fine particles in July 1997, we issued a guidance
document ``Interim Implementation for the New Source Review
Requirements for PM2.5,'' John S. Seitz, Director, Office of
Air Quality Planning and Standards, EPA, October 23, 1997. As noted in
that guidance, section 165 of the Act implies that PSD requirements
become effective for a new NAAQS upon the effective date of the NAAQS.
Section 165(a)(1) of the Act provides that no new or modified major
source may be constructed without a PSD permit that meets all of the
section 165(a) requirements with respect to the regulated pollutant.
Moreover, section 165(a)(3) provides that the emissions from any such
source may not cause or contribute to a violation of any increment or
NAAQS. Also, section 165(a)(4) requires BACT for each pollutant subject
to PSD regulation. The 1997 guidance stated that sources would be
allowed to use implementation of a PM10 program as a
surrogate for meeting PM2.5 NSR requirements until certain
difficulties were resolved. These difficulties included the lack of
necessary tools to calculate the emissions of PM2.5 and
related precursors, the lack of adequate modeling techniques to project
ambient impacts, and the lack of PM2.5 monitoring sites.
On April 5, 2005, we issued a guidance document entitled
``Implementation of New Source Review Requirements in PM-2.5
Nonattainment Areas,'' Stephen D. Page, Director, Office of Air Quality
Planning and Standards, EPA. This memorandum provides guidance on the
implementation of the nonattainment major NSR provisions in
PM2.5 nonattainment areas in the interim period between the
effective date of the PM2.5 NAAQS designations (April 5,
2005) and when we promulgate regulations to implement nonattainment
major NSR for the PM2.5 NAAQS. In addition to affirming the
continued use of the John S. Seitz guidance memo in PM2.5
attainment areas, this memo recommends that until we promulgate the
PM2.5 major NSR regulations, States should use a
PM10 nonattainment major NSR program as a surrogate to
address the requirements of nonattainment major NSR for the
PM2.5 NAAQS.
On November 1, 2005, we proposed a rule to implement the
PM2.5 NAAQS, including proposed revisions to the NSR
program. For those States with EPA-approved PSD programs, we proposed
to continue the 1997 NSR guidance to use PM10 as a surrogate
for PM2.5, but only during the SIP development period. We
also indicate in that proposal that we will develop increments, SILs,
and SMC in a separate rulemaking--i.e. this proposed rulemaking. Since
there was an interim surrogate NSR program in place, EPA decided to
first promulgate the non-NSR part of the implementation rule (including
attainment demonstrations, designations, control measures etc.)--which
was promulgated on April 25, 2007. The NSR part of the implementation
rule is anticipated to be promulgated in September 2007. Additionally,
once this proposed rulemaking is finalized, States will be able to
fully implement a PM2.5 NSR program.
D. Background on Implementation of PSD Increments
Under section 165(a)(3) of the Act, a PSD permit applicant must
demonstrate that emissions from the proposed construction and operation
of a facility ``will not cause, or contribute to, air pollution in
excess of any (A) maximum allowable increase or maximum allowable
concentration for any pollutant. * * *'' 42 U.S.C. 7475(a)(3). The
``maximum allowable increase'' of an air pollutant that is allowed to
occur above the applicable baseline concentration for that pollutant is
known as the PSD increment. By establishing the maximum allowable level
of ambient pollutant concentration increase in a particular area, an
increment defines ``significant deterioration.''
For PSD baseline purposes, a baseline area for a particular
pollutant emitted from a source includes the attainment or
unclassifiable area in which the source is located as well as any other
attainment or unclassifiable area in which the source's emissions of
that pollutant are projected (by air quality modeling) to result in an
ambient pollutant increase of at least 1 [mu]g/m\3\ (annual average).
See, e.g., 40 CFR 52.21(b)(15)(i). Once the baseline area is
established, subsequent PSD sources locating in that area need to
consider that a portion of the available increment may have already
been consumed by previous emissions increases.
In general, the submittal date of the first complete PSD permit
application in a particular area is the operative
[[Page 54117]]
``baseline date.'' \3\ On or before the date of the first complete PSD
application, emissions generally are considered to be part of the
baseline concentration, except for certain emissions from major
stationary sources, as explained in the following discussion of
baseline dates. Most emissions increases that occur after the baseline
date will be counted toward the amount of increment consumed.
Similarly, emissions decreases after the baseline date restore or
expand the amount of increment that is available.
---------------------------------------------------------------------------
\3\ Baseline dates are pollutant specific. That is, a complete
PSD application establishes the baseline date only for those
regulated NSR pollutants that are projected to be emitted in
significant amounts (as defined in the regulations) by the
applicant's new source or modification. Thus, an area may have
different baseline dates for different pollutants.
---------------------------------------------------------------------------
In practice, three dates related to the PSD baseline concept are
important in understanding how to calculate the amount of increment
consumed--(1) Trigger date; (2) minor source baseline date; and (3)
major source baseline date. Chronologically, the first relevant date is
the trigger date. The trigger date, as the name implies, triggers the
overall increment consumption process nationwide. Specifically, this is
a fixed date, which must occur before the minor source baseline date
can be established for the pollutant-specific increment in a particular
attainment area. See, e.g., 40 CFR 52.21(b)(14)(ii). For PM and
SO2, Congress defined the applicable trigger date as August
7, 1977--the date of the 1977 amendments to the Act when the original
statutory increments were established by Congress. For NO2,
we selected the trigger date as February 8, 1988--the date on which we
proposed increments for NO2. See 53 FR 40656, 40658; October
17, 1988. In this action, as described later, we are proposing to add a
new trigger date for purposes of calculating the new PM2.5
increments.
The two remaining dates--``minor source baseline date'' and ``major
source baseline date''--as described later, are necessary to properly
account for the emissions that are to be counted toward increment
consumed following the national trigger date, in accordance with the
statutory definition of ``baseline concentration'' in section 169(4) of
the Act. The statutory definition provides that the baseline
concentration of a pollutant for a particular baseline area is
generally the air quality at the time of the first application for a
PSD permit in the area. Consequently, any increases in actual emissions
occurring after that date (with some possible exceptions that we will
discuss later) would be considered to consume the applicable PSD
increment. However, the statutory definition in section 169(4) also
provides that ``[E]missions of sulfur oxides and particulate matter
from any major emitting facility on which construction commenced after
January 6, 1975 shall not be included in the baseline and shall be
counted in pollutant concentrations established under this part.''
To make this distinction between the date when emissions changes in
general (i.e., from both major and minor sources) affect the increment
and the date when emissions resulting from the construction at a major
stationary source consume the increment, we established the terms
``minor source baseline date'' and ``major source baseline date,''
respectively. See 40 CFR 51.166(b)(14) and 52.21(b)(14). Accordingly,
the ``minor source baseline date'' is the date on which the first
complete application for a PSD permit is filed in a particular area.
Any change in actual emissions after that date affects the PSD
increment for that area.
The ``major source baseline date'' is the date after which actual
emissions increases associated with construction at any major
stationary source affect the PSD increment. In accordance with the
statutory definition of ``baseline concentration,'' the PSD regulations
define a fixed date to represent the major source baseline date for
each pollutant for which an increment exists. Congress defined the
major source baseline date for the statutory increments for PM and
SO2 as January 6, 1975. For the NO2 increments,
which we promulgated in 1988 under our authority to establish an
increment system under section 166(a) of the Act, the major source
baseline date we selected is February 8, 1988--the date on which we
proposed increments for NO2. 53 FR 40656. In this action, as
described later, we are proposing to add a new major source baseline
date for PM2.5.
The PSD regulations set out the third date that is relevant to the
PSD baseline concept. These regulations provide that the earliest date
on which the minor source baseline date can be established is the date
immediately following the ``trigger date'' for the pollutant-specific
increment. See, e.g., 40 CFR 52.21(b)(14)(ii). For PM and
SO2, Congress defined the applicable trigger date as August
7, 1977--the date of the 1977 amendments to the Act when the original
statutory increments were established by Congress. For NO2,
we selected the trigger date as February 8, 1988--the date on which we
proposed increments for NO2. See 53 FR 40656, 40658; October
17, 1988.
Once the minor source baseline date associated with the first PSD
permit application for a proposed new major stationary source or major
modification in an area is established, the new emissions from that
source consume a portion of the increment in that area, as do any
subsequent actual emissions increases that occur from any new or
existing source in the area. When the maximum pollutant concentration
increase defined by the increment has been reached, additional PSD
permits cannot be issued until sufficient amounts of the increment are
``freed up'' via emissions reductions that may occur voluntarily, e.g.,
via source shutdowns, or via control requirements imposed by the
reviewing authority. Moreover, the air quality in a region cannot
deteriorate to a level in excess of the applicable NAAQS, even if all
the increment has not been consumed. Therefore, new or modified sources
located in areas where the air pollutant concentration is near the
level allowed by the NAAQS may not have full use of the amount of
pollutant concentration increase allowed by the increment.
Under EPA guidance, the actual increment analysis that a proposed
new or modified source undergoing PSD review must complete depends on
the area impacted by the source's new emissions.\4\ We have also
provided approved air quality models and guidelines for sources to use
to project the air quality impact of each pollutant (over each
averaging period) for which an increment analysis must be done.\5\ In
addition, we established significant impact levels for each pollutant
under the nonattainment major NSR program that have also been used
under the PSD program to identify levels below which the source's
modeled impact is regarded as de minimis. See 40 CFR 51.165(b) and part
51, appendix S, section III.A. In the event that a source's modeled
impacts of a particular pollutant are below the applicable significant
impact level at all ambient air locations modeled, i.e., de minimis
everywhere, EPA policy provides that no further modeling analysis is
required for that pollutant. Our policy is that when a preliminary
screening analysis based on the significant impact level is sufficient
to demonstrate that the source's
[[Page 54118]]
emissions will not cause or contribute to a violation of the increment,
there is no need for a full impacts analysis involving a cumulative
evaluation of the emissions from the proposed source and other sources
affecting the area.
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\4\ We note that on June 6, 2007, we published a notice of
proposed rulemaking proposing to refine several aspects of the
increment calculation process to clarify how States and regulated
sources may calculate increases in pollutant concentrations for
purposes of determining compliance with the PSD increments. See 72
FR at 31372. When final, these revisions will amend the PSD
regulations at 40 CFR 51.166 and 52.21.
\5\ See EPA's ``Guideline on Air Quality Models'' at 40 CFR part
51, appendix W.
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Within the impact area of a source that does have a significant
impact, increment consumption is calculated using the source's proposed
emissions increase, along with other emissions increases or decreases
of the particular pollutant from sources in the area, which have
occurred since the minor source baseline date established for that
area. (For major sources, emissions increases or decreases that have
occurred since the major source baseline date consume or expand
increment.) Thus, an emissions inventory of sources whose emissions
consume or expand the available increment in the area must be compiled.
The inventory includes not only sources located directly in the impact
area, but sources outside the impact area that affect the air quality
within the impact area.
The inventory of emissions includes emissions from increment-
affecting sources at two separate time periods--the baseline date and
the current period of time. For each source that was in existence on
the relevant baseline date (major source or minor source), the
inventory includes the source's actual emissions on the baseline date
and its current actual emissions. The change in emissions over these
time periods represents the emissions that consume increment (or, if
emissions have gone down, expand the available increment). For sources
constructed since the relevant baseline date, all their current actual
emissions consume increment and are included in the inventory.
When the inventory of emissions has been compiled, computer
modeling is used to determine the change in ambient concentration that
will result from these emissions when combined with the proposed
emissions increase from the new major source or major modification that
is undergoing PSD review. The modeling has generally been guided by the
``Guideline on Air Quality Models'' (40 CFR part 51, appendix W), which
includes provisions on air quality models and the meteorological data
input into these models. The model output (expressed as a change in
concentration) for each relevant averaging period is then compared to
the corresponding allowable PSD increment.
E. Historical Approaches for Developing Increments
1. Congressional Enactment of Increments for PM and SO2
Congress established the first increments defining significant
deterioration of air quality in the 1977 Amendments to the Act. These
amendments to the Act, among other things, added subpart C to title I,
setting out the requirements for PSD. In section 163, Congress included
numerical increments for PM and sulfur dioxide (SO2) for
Class I, II, and III areas.
The three area classes are part of the increment system originally
established by Congress. Congress designated Class I areas (including
certain national parks and wilderness areas) as areas of special
national concern, where the need to prevent deterioration of air
quality is the greatest. Consequently, the allowable level of
incremental change is the smallest relative to the other area classes,
i.e., most stringent, in Class I areas. The increments of Class II
areas are larger than those of Class I areas and allow for a moderate
degree of emissions growth. For future redesignation purposes, Congress
defined as Class III any existing Class II area for which a State may
desire to promote a higher level of industrial development (and
emissions growth). Thus, Class III areas are allowed to have the
greatest amount of pollutant increase of the three area classes while
still achieving the NAAQS. There have been no Class III redesignations
to date.
In establishing these PSD increments, Congress used the then-
existing NAAQS for those pollutants as the benchmark for determining
what constitutes ``significant deterioration.'' Congress established
the increments for PM as a percentage of the then-existing PM NAAQS. At
the time the Act was amended in 1977, the NAAQS for PM were expressed
in terms of ambient concentrations of total suspended particulate
(TSP). Thus, EPA interpreted the statutory increments for PM using the
same ambient ``indicator.''
2. EPA's Promulgation of Increments for NO2 and
PM10
Congress also provided authority for EPA to promulgate additional
increments and to update the original PM increments created by statute.
The EPA has promulgated two regulations pursuant to this authority.
a. Increments for NOX Using the ``Contingent Safe Harbor''
Approach Under Section 166(a) of the Act
As enacted in 1977, subpart C of the Act also included sections
166(a) through 166(e), which set out requirements related to increments
for other pollutants. Section 166(a) requires EPA to develop
regulations to prevent the significant deterioration of air quality due
to emissions of certain named pollutants, and to develop such
regulations for any pollutants for which NAAQS are subsequently
promulgated. Section 166(b) prescribes timelines for the effective date
of such regulations, and for corresponding SIP submittals and EPA
approvals. Specifically, regulations, including increments, developed
pursuant to section 166(a) become effective 1 year after the date of
promulgation, and State plan revisions containing the new regulations
are to be submitted to EPA for review within 21 months of promulgation.
The same provision then calls for EPA's approval or disapproval of the
revised plan within 25 months of promulgation. The legislative history
indicates that this 1-year delay before the new PSD requirements,
including the new increments, become effective is to allow Congress an
opportunity to review them before States are required to implement
them. H.R. Conf. Rep. 95-564, at 151 (1977), 1977 U.S.C.C.A.N. 1502,
1532. Section 166(c) and (d) set forth criteria and goals that such
regulations must meet.
Based on section 166 of the Act, on October 17, 1988, EPA
promulgated increments for nitrogen dioxide (NO2) to prevent
significant deterioration of air quality due to emissions of
NOX (53 FR 40656). The EPA based these increments on
percentages of the NAAQS in the same way that Congress derived the
statutory increments for PM and SO2. Those NO2
increments were challenged in 1988 by the Environmental Defense Fund
(now Environmental Defense, or ``ED'') when ED filed suit in the U.S.
Court of Appeals for the District of Columbia Circuit against the
Administrator (Environmental Defense Fund, Inc. v. Reilly, No. 88-
1882). Environmental Defense successfully argued that we failed to
sufficiently consider certain provisions in section 166 of the Act. The
court remanded the case to EPA ``to develop an interpretation of
section 166 that considers both subsections (c) and (d), and if
necessary to take new evidence and modify the regulations.'' See
Environmental Defense Fund v. EPA, 898 F.2d 183, 190 (D.C. Cir. 1990).
Section 166(c) of the Act requires the PSD regulations to, among other
things, meet the goals and purposes set forth in sections 101 and 160
of the Act. Section 166(d) requires these regulations be at least as
effective as the increments
[[Page 54119]]
established for PM (in the form of TSP) and SO2 in section
163 of the Act. The court considered the NO2 increment
values determined using the percentage-of-NAAQS approach as ``safe
harbor'' increments which met the requirements of section 166(d) of the
Act. However, the court also determined that EPA's reliance on such
increment levels was contingent upon our completing the analyses
required under section 166(c), which provided that the final increment
values must address the goals of sections 101 and 160 of the Act to
protect public health and welfare, parks, and air quality related
values (AQRVs) \6\ and to ensure economic growth.
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\6\ The term ``air quality related values'' is not defined in
the Act, but the legislative history provides that ``The term `air
quality related values' of Federal lands designated as class I
includes the fundamental purposes for which such lands have been
established and preserved by the Congress and the responsible
Federal agency. For example, under the 1916 Organic Act to establish
the National Park Service (16 U.S.C. 1), the purpose of such
national park lands `is to conserve the scenery and the natural and
historic objects and the wildlife therein and to provide for the
enjoyment of the same in such manner and by such means as will leave
them unimpaired for the enjoyment of future generations.' '' S. Rep.
No. 95-127 at 36 (1977)
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In response to the court's decision, we proposed rulemaking on
increments for NOX on February 23, 2005 (70 FR 8880) and
finalized the rule on October 12, 2005 (70 FR 59582). In the final
rule, we established our policy on how to interpret and apply the
requirements of sections 166(c) and (d) of the Act. In accordance with
the court ruling, we conducted further analyses (considering the health
and welfare effects of NOX) and concluded that the existing
NO2 increments were adequate to fulfill the requirements of
section 166(c). See 70 FR 59586 for our detailed analysis of how
pollutant regulations satisfy the requirements of section 166 of the
Act. Hence, we retained the existing NO2 increments along
with other parts of the existing framework of pollutant-specific PSD
regulations for NOX. We also amended the requirements of 40
CFR 51.166 to make it clear that States may seek EPA approval of SIPs
that utilize a different approach than EPA used to establish these
NO2 increments. To receive our approval of an alternative
program, a State must demonstrate that its program satisfies the
requirements of sections 166(c) and 166(d) of the Act and prevents
significant deterioration of air quality from emissions of
NOX.\7\
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\7\ Under the 2005 NOX regulation, States can adopt
measures other than increments as long as they can demonstrate that
the measures selected comply with the same criteria and goals of 166
(c) and (d) of the Act that must be met for increments.
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b. Increments for PM10 Using ``Equivalent Substitution''
Approach Under Section 166(f)
On October 5, 1989, we proposed new PM10 increments. See
54 FR 41218. Although section 163 did not expressly define the existing
statutory increments for PM in terms of a specific indicator, EPA
reasoned that Congress's knowledge that TSP was the indicator for the
PM NAAQS, and that the TSP standards were the starting point for the
increments levels when the increments were established in 1977, meant
that TSP was also the appropriate measure for the PM increments in
section 163. As a consequence, EPA believed that the statutory PM
increments could not simply be administratively redefined as
PM10 increments, retaining the same numerical values,
following the revision of the PM NAAQS. Rather, we stated our belief
that with the promulgation of the PM10 NAAQS, EPA had both
the responsibility and the authority under sections 166 and 301 of the
Act to promulgate new increments for PM to be measured in terms of
PM10. We further concluded that promulgating PM10
increments to replace, rather than supplement, the statutory TSP
increments under section 163 represented the most sensible approach for
preventing significant deterioration with respect to PM. See 54 FR
41220-41221.
We promulgated PM10 increments to replace the existing
TSP increments on June 3, 1993 (58 FR 31622). In the interim between
proposal and promulgation, Congress enacted the 1990 Act Amendments. As
part of these Act Amendments, Congress amended section 166 to add a new
section 166(f). This section specifically authorized EPA to substitute
PM10 increments for the existing section 163 PM increments
based on TSP, provided that the substituted increments are ``of equal
stringency in effect'' as the section 163 increments.
Thus, we were able to replace the TSP increments under section 163
of the Act using PM10 increments based directly on the newly
enacted authority under section 166(f) of the Act. In the
PM10 rule, we maintained the existing baseline dates and
baseline areas for PM that had been previously established using the
TSP indicator. Also as proposed, we promulgated PM10
increments developed based on an approach we called the ``equivalent to
statutory increments'' approach. Under this approach, we used the
original TSP increments as a benchmark for calculating the
PM10 increments, thereby retaining roughly the same
limitations on future deterioration of air quality as was allowed under
the TSP increments. In using this approach, we considered the
historical consumption of TSP increment by a sample population of
permitted PSD sources, and then determined the PM10
increments for each area classification and averaging time that would
provide approximately the same percentage of PM10 increment
consumption, on average, by the same population of sources. Then, all
future calculations of increment consumption after the PM10
implementation date would be based on PM10 emissions. See 58
FR 31622 and 31625.
IV. EPA'S Interpretation of Section 166 of the Clean Air Act
A. Which Criteria in Section 166 Should EPA Use to Develop Increments
for PM2.5?
The EPA interprets section 166 of the Act to give the Administrator
the discretion to use either the ``contingent safe harbor'' approach or
the ``equivalent substitution'' approach to establish increments for
PM2.5. Since sections 166(a) and section 166(f) contain or
incorporate different criteria for establishing PSD regulations
containing increments or other measures, the interpretation that EPA
chooses to follow could have an impact on the increments or other
measures that EPA adopts. Regulations promulgated under section 166(a)
must be based on the criteria in section 166(c) and 166(d). 42 U.S.C.
7476(c)-(d). Regulations promulgated under section 166(f) must ``be of
equal stringency in effect as those specific in the provisions for
which they are substituted.'' 42 U.S.C. 7476(f). Furthermore, section
166(a) calls broadly for regulations, which may include increments,
whereas section 166(f) addresses only increments.
Section 166(a) provides authority for EPA to promulgate additional
pollutant-specific PSD regulations, which may include increments, for
the pollutants specifically identified in that provision plus
additional pollutants for which EPA may promulgate a NAAQS after a
specific date 42 U.S.C. 7476(a). The last sentence of section 166(a)
provides the following:
In the case of pollutants for which national ambient air quality
standards are promulgated after August 7, 1977, [the Administrator]
shall promulgate such regulations not more than 2 years after the
date of promulgation of such standards.
Since EPA promulgated an additional NAAQS for PM, based on the
PM2.5 indicator, in 1997, one potential
[[Page 54120]]
approach for developing increments for PM2.5 is for EPA to
promulgate these increments under the authority of section 166(a).
Under this approach, EPA would promulgate increments or other measures
for PM2.5 that satisfy the standards set forth in
subsections (c) and (d) of section 166, as interpreted by EPA in our
recent rulemaking for nitrogen oxides.
However, in light of the provisions in section 163 and 166(f) of
the Act that address increments for TSP and PM10,
respectively, there is some ambiguity on the question of the legal
authority EPA should rely upon to establish increments for
PM2.5. In 1993, EPA construed section 166(f) to establish
the sole criteria for promulgation of a new PM increment and thus did
not base our final PM10 increment on section 166(a) of the
Act. Considering sections 163, 166(a), and 166(f) together, an
alternative interpretation of these provisions might be that Congress
intended that section 163 and 166(f) alone cover PM. Under this
reading, EPA would promulgate additional increments for particular
matter based on the section 163 increments and 166(f) of the Act, which
are the only provisions that specifically mention PM and PSD
increments. However, as discussed later, it may also be possible to
read sections 166(a) and 166(f) in harmony. Thus, we propose to adopt
one of the following legal theories to support promulgation of
increments for PM2.5 using either of the two methods that
EPA used in prior rules to develop PSD increments.
1. Support for ``Contingent Safe Harbor'' Approach for PM2.5
Under Section 166(a)
The EPA believes it is permissible to interpret section 166(a) to
apply to PM2.5. Although EPA has generally characterized the
NAAQS for PM2.5 as a NAAQS for a new indicator of PM, EPA
did not replace the PM10 NAAQS with the NAAQS for
PM2.5 in 1997. Rather, EPA established an additional NAAQS
for PM2.5 as if it were a new pollutant, even though EPA had
already developed air quality criteria for PM generally. Thus, for
purposes of section 166(a), the addition of a NAAQS for
PM2.5