Drinking Water: Final Action on Perchlorate, 43990-44002 [2020-13462]
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Federal Register / Vol. 85, No. 140 / Tuesday, July 21, 2020 / Rules and Regulations
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You may submit comments on any
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10.115(g)(5)).
Submit written requests for single
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the SUPPLEMENTARY INFORMATION section
for electronic access to the guidance
document.
FOR FURTHER INFORMATION CONTACT:
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Food and Drug Administration, 10903
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SUPPLEMENTARY INFORMATION:
I. Background
FDA is announcing the availability of
a document entitled ‘‘Regulatory
Considerations for Human Cells,
Tissues, Cellular and Tissue-Based
Products: Minimal Manipulation and
Homologous Use.’’ This guidance is
being issued consistent with FDA’s good
guidance practices regulation (§ 10.115
(21 CFR 10.115)). The Agency is
soliciting public comment, but is
implementing this guidance
immediately, because the Agency has
determined that prior public
participation is not feasible or
appropriate. Although this guidance
document is immediately in effect, it
remains subject to comment in
accordance with FDA’s good guidance
practices regulation.
The guidance does not alter FDA’s
current thinking on the regulatory
criteria of minimal manipulation and
homologous use for human cells,
tissues, and cellular and tissue-based
product (HCT/P) as described in the
November 2017 guidance of the same
name and corrected in December 2017.
The only substantive change to this
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guidance is to revise section V of the
November 2017 guidance to
communicate that FDA intends to
exercise enforcement discretion for
certain regulatory requirements for
certain HCT/Ps for a longer period of
time, i.e., through May 31, 2021, instead
of November 30, 2020. This will give
manufacturers additional time to
determine if they need to submit an
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additional time is warranted in light of
the Coronavirus Disease 2019 (COVID–
19) public health emergency, which has
presented unique challenges in
recruiting clinical trial participants and
carrying out clinical trials.
As described in the guidance, FDA
generally intends to exercise
enforcement discretion with respect to
the IND and the premarket approval
requirements for HCT/Ps that do not
meet one or more of the 21 CFR
1271.10(a) criteria, provided that use of
the HCT/P does not raise reported safety
concerns or potential significant safety
concerns. FDA intends to continue to
focus enforcement actions on products
with higher risk, including based on the
route and site of administration.
This guidance is being issued
consistent with FDA’s good guidance
practices regulation (§ 10.115(g)(2)). The
guidance represents the current thinking
of FDA on ‘‘Regulatory Considerations
for Human Cells, Tissues, and Cellular
and Tissue-Based Products: Minimal
Manipulation and Homologous Use.’’ It
does not establish any rights for any
person and is not binding on FDA or the
public. You can use an alternative
approach if it satisfies the requirements
of the applicable statutes and
regulations.
II. Paperwork Reduction Act of 1995
This guidance contains no collection
of information. Therefore, clearance by
the Office of Management and Budget
(OMB) under the Paperwork Reduction
Act of 1995 (PRA) (44 U.S.C. 3501–
3521) is not required.
However, this guidance refers to
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information found in FDA regulations.
These collections of information are
subject to review by OMB under the
PRA. The collections of information in
21 CFR part 1271 have been approved
under OMB control number 0910–0543.
III. Electronic Access
Persons with access to the internet
may obtain the guidance at https://
www.fda.gov/vaccines-blood-biologics/
guidance-compliance-regulatory-
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information-biologics/biologicsguidances; https://www.fda.gov/
medical-devices/device-advicecomprehensive-regulatory-assistance/
guidance-documents-medical-devicesand-radiation-emitting-products;
https://www.fda.gov/combinationproducts/guidance-regulatoryinformation; or https://
www.regulations.gov.
Dated: July 15, 2020.
Lowell J. Schiller,
Principal Associate Commissioner for Policy.
[FR Doc. 2020–15718 Filed 7–20–20; 8:45 am]
BILLING CODE 4164–01–P
ENVIRONMENTAL PROTECTION
AGENCY
40 CFR Parts 141 and 142
[EPA–HQ–OW–2018–0780, EPA–HQ–OW–
2008–0692, EPA–HQ–OW–2009–0297; FRL–
10011–21–OW]
RIN 2040–AF28
Drinking Water: Final Action on
Perchlorate
Environmental Protection
Agency (EPA).
ACTION: Final action.
AGENCY:
The Environmental Protection
Agency (EPA) is announcing its
withdrawal of the 2011 determination to
regulate perchlorate in accordance with
the Safe Drinking Water Act, (SDWA).
On February 11, 2011, the EPA
published a Federal Register document
in which the Agency determined that
perchlorate met the SDWA’s criteria for
regulating a contaminant. On June 26,
2019, the EPA published a proposed
national primary drinking water
regulation (NPDWR) for perchlorate and
requested public comments on multiple
alternative actions, including the
alternative of withdrawing the 2011
regulatory determination for
perchlorate. The EPA received
approximately 1,500 comments on the
proposed rulemaking. The EPA has
considered these public comments and
based on the best available information
the Agency is withdrawing the 2011
regulatory determination and is making
a final determination not to regulate
perchlorate. The EPA has determined
that perchlorate does not occur ‘‘with a
frequency and at levels of public health
concern’’ within the meaning of the
SDWA. In addition, in the judgment of
the EPA Administrator, regulation of
perchlorate does not present a
‘‘meaningful opportunity for health risk
reduction for persons served by public
water systems.’’ Accordingly, the EPA is
SUMMARY:
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Federal Register / Vol. 85, No. 140 / Tuesday, July 21, 2020 / Rules and Regulations
withdrawing its 2011 determination and
is making a final determination not to
regulate perchlorate, and therefore will
not issue a NPDWR for perchlorate at
this time.
For purposes of judicial review,
the regulatory determination in this
document is issued as of July 21, 2020.
DATES:
FOR FURTHER INFORMATION CONTACT:
Samuel Hernandez, Office of Ground
Water and Drinking Water, Standards
and Risk Management Division (Mail
Code 4607M), Environmental Protection
Agency, 1200 Pennsylvania Avenue
NW, Washington, DC 20460; telephone
number: (202) 564–1735; email address:
hernandez.samuel@epa.gov.
This
document is organized as follows:
SUPPLEMENTARY INFORMATION:
I. General Information
A. Does this action apply to me?
B. How can I get copies of this document
and other related information?
II. Background
A. What is perchlorate?
B. What is the purpose of this action?
C. What is the EPA’s statutory authority for
this action?
D. Statutory Framework and Perchlorate
Regulatory History
III. Withdrawal of the 2011 Regulatory
Determination and Final Determination
Not To Regulate Perchlorate
A. May perchlorate have an adverse effect
on the health of persons?
B. Is perchlorate known to occur or is there
a substantial likelihood that perchlorate
will occur in public water systems with
a frequency and at levels of public health
concern?
C. Is there a meaningful opportunity for the
reduction of health risks from
perchlorate for persons served by public
water systems?
D. What is the EPA’s final regulatory
determination on perchlorate?
IV. Summary of Key Public Comments on
Perchlorate
A. SDWA Statutory Requirements and the
EPA’s Authority
B. Health Effects Assessment
C. Occurrence Analysis
V. Conclusion
VI. References
I. General Information
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A. Does this action apply to me?
This action will not impose any
requirements on anyone. Instead, this
action notifies interested parties of the
EPA’s withdrawal of the 2011 regulatory
determination for perchlorate and the
final regulatory determination not to
regulate perchlorate. Section IV of this
document provides a summary of the
key comments received on the June 26,
2019 (84 FR 30524) proposed NPDWR
for perchlorate (referred to hereinafter as
‘‘the 2019 proposal’’).
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B. How can I get copies of this document B. What is the purpose of this action?
and other related information?
The purpose of this action is to
publish the EPA’s notice to withdraw
The EPA has established a docket for
the 2011 regulatory determination, one
this action under Docket ID No. EPA–
HQ–OW–2018–0780. Publicly available of the alternative options in the 2019
proposal, and to issue a final
docket materials are available
determination not to regulate
electronically at https://
perchlorate in drinking water. This
www.regulations.gov/docket?D=EPAdocument presents the EPA’s basis for
HQ-OW-2018-0780.
this withdrawal and final regulatory
II. Background
determination, and the EPA’s response
to key issues raised by commenters in
A. What is perchlorate?
response to the 2019 proposal.
Perchlorate is a negatively charged
C. What is the EPA’s statutory authority
inorganic ion that is composed of one
for this action?
chlorine atom bound to four oxygen
atoms (ClO4-), which is highly stable
The SDWA sets forth three criteria
and mobile in the aqueous environment. that must be met for the EPA to issue
Perchlorate comes from both natural
a maximum contaminant level goal
and manmade sources. It is formed
(MCLG) and promulgate a national
naturally via atmospheric processes and primary drinking water regulation
can be found within mineral deposits in (NPDWR). Specifically, the
certain geographical areas. It is also
Administrator must determine that (1)
produced in the United States by
‘‘the contaminant may have an adverse
industrial processes, and the most
effect on the health of persons’’; (2) ‘‘the
commonly produced compounds
contaminant is known to occur or there
include ammonium perchlorate and
is a substantial likelihood that the
potassium perchlorate used primarily as contaminant will occur in public water
oxidizers in solid fuels to power rockets, systems with a frequency and at levels
missiles, and fireworks. Perchlorate can of public health concern’’; and (3) ‘‘in
also result from the degradation of
the sole judgment of the Administrator,
hypochlorite solutions used for water
regulation of such contaminant presents
disinfection. The degradation into
a meaningful opportunity for health risk
perchlorate occurs when hypochlorite
reduction for persons served by public
solutions are improperly stored and
water systems’’ (SDWA 1412(b)(1)(A)).
handled. For the general population,
SDWA 1412(b)(1)(B) sets out the
most perchlorate exposure is through
process for the EPA to establish
the ingestion of contaminated food or
drinking water standards for an
drinking water. Above certain levels,
unregulated contaminant. As explained
perchlorate can prevent the thyroid
in more detail below, in 2011, the EPA
gland from getting enough iodine,
issued a determination that perchlorate
which can affect thyroid hormone
met the three statutory criteria outlined
production. The consequences of
above and therefore should be regulated.
insufficient thyroid hormone levels
Under the statute, a determination to
during human growth and development regulate triggers a duty for the EPA to
are well known. For pregnant women
issue a proposed drinking water
with low iodine levels, sufficient
standard within two years and a final
changes in thyroid hormone levels may
rule 18 months later (with the
cause changes in the child’s brain
possibility of a 3 month extension).
development. In a 2005 report entitled
SDWA 1412(b)(1)(E). The EPA
‘‘Health Implications of Perchlorate
subsequently published a proposed
Ingestion’’, the National Research
drinking water standard for perchlorate,
Council stated that: ‘‘fetuses and
and alternatives including the
preterm newborns constitute the most
withdrawal of the 2011 regulatory
sensitive populations although infants
determination, in 2019. The
and developing children are also
promulgation of a final drinking water
considered sensitive populations’’ (NRC, standard would, when effective, require
2005). The existence of a quantifiable
monitoring of public water supplies for
relationship between thyroid hormone
the contaminant and treatment as
changes and neurodevelopmental
necessary to meet the regulatory
outcomes has strong support from the
standard.
The EPA has determined, based on
literature on the subject; however, not
reviewing data and analysis obtained
every study identifies an association
since the issuance of the 2011 regulatory
between maternal thyroid hormone
determination, that perchlorate does not
levels and the neurodevelopmental
meet the statutorily-prescribed criteria
outcomes, and the state of the science
for regulation. As described in Sections
on this relationship is constantly
III & VI of the 2019 proposal, the data
evolving.
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Federal Register / Vol. 85, No. 140 / Tuesday, July 21, 2020 / Rules and Regulations
and analysis in the record indicate that
perchlorate does not occur in public
water systems with a frequency and at
levels of public health concern.
Specifically, the peer-reviewed health
effects analysis indicates that the
estimated concentrations of perchlorate
that may represent levels of public
health concern (i.e., the proposed MCLG
levels, 18–90 mg/L) is higher than the
concentration considered in issuance of
the 2011 regulatory determination (1–47
mg/L) (USEPA, 2019a). In addition,
based on a re-evaluation of the
nationally representative First
Unregulated Contaminant Monitoring
Rule (UCMR 1) data, the updated
occurrence analysis shows that the
frequency of occurrence of perchlorate
in public water systems at levels
exceeding any of the alternative
proposed MCLGs (18 mg/L–90 mg/L) is
significantly lower (0.03%–0.002%)
than the frequency considered in the
analysis for the 2011 regulatory
determination (4%–0.39%) (USEPA,
2019b). The EPA estimates that, even at
the most stringent regulatory level
considered in the 2019 proposal (18 mg/
L), not more than 15 systems (0.03% of
all water systems in the U.S. serving
approximately 620,000 people) would
need to take action to reduce levels of
perchlorate. Based on this information,
the EPA determines that perchlorate
does not occur in public water systems
‘‘with a frequency and at levels of
public health concern’’ and thus does
not meet the second criterion of the
three required for regulation under the
SDWA. In addition, while the third
criterion is ‘‘in the sole judgment of the
Administrator,’’ the small number of
water systems with perchlorate levels
greater than identified thresholds, and
the correspondingly small population
served, provides ample support for the
EPA’s conclusion that the regulation of
perchlorate does not present a
‘‘meaningful opportunity for health risk
reduction for persons served by public
water systems,’’ within the meaning of
1412(b)(1)(A)(iii). Accordingly, because
perchlorate no longer meets the
statutory criteria for regulation, the EPA
does not have the authority to issue a
MCLG or promulgate a NPDWR for
perchlorate.
While the EPA has not previously
withdrawn a regulatory determination,
the decision is supported by the
legislative history underlying the 1996
amendments to the SDWA, which
repealed the statutory requirement for
the EPA to regulate an additional 25
contaminants every 3 years and
replaced it with the current requirement
for the EPA to determine whether
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regulation is warranted for five
contaminants every five years. In
describing the need for such
amendment, the legislative history
points to the view expressed at the
Committee Hearing that ‘‘the current
law is a one-size-fits-all program. It
forces our water quality experts to
spend scarce resources searching for
dangers that often do not exist rather
than identifying and removing real
health risks from our drinking water’’
(S. Rep. 104–169 (1995) at 12). This
amendment reflected Congress’ clear
intent that the EPA prioritize actual
health risks in determining whether to
regulate any particular contaminant. See
id at 12 (noting that the amendment
‘‘repeals the requirement that the EPA
regulate an additional 25 contaminants
every 3 years replacing it with a new
selection process that gives the EPA the
discretion to identify contaminants that
warrant regulation in the future’’).
The EPA’s decision to withdraw the
regulatory determination is also
consistent with Congress’ direction to
prioritize SDWA decisions based on the
best available public health information.
See 1412(b)(1)(B)(ii)(II) (findings
supporting a determination to regulate
‘‘shall be based on the best available
public health information’’);
1412(b)(2)(A) (requiring that the EPA
use ‘‘the best available, peer-reviewed
science and supporting studies . . .’’ in
carrying out any actions under this
section). Although the EPA determined
in 2011 that perchlorate met the criteria
for regulation, new data and analysis
developed by the Agency as part of the
2019 proposal demonstrate that the
occurrence and health effects
information used as the basis for the
2011 determination no longer constitute
‘‘best available information,’’ are no
longer accurate, and no longer support
the Agency’s prioritization of
perchlorate for regulation. Accordingly,
not only is the EPA not authorized to
issue a MCLG or promulgate a NPDWR
for perchlorate, but it would not be in
the public interest for the EPA to do so.
The EPA recognizes that the SDWA
does not include a provision explicitly
authorizing withdrawal of a regulatory
determination. However, such authority
is inherent in the authority to issue a
regulatory determination under
1412(b)(1)(B)(ii)(II), particularly given
the requirement that such determination
be based on the ‘‘best available public
health information,’’ as discussed above.
Accordingly, the EPA must have the
inherent authority to withdraw a
regulatory determination if the
underlying information changes
between regulatory determination and
promulgation. In light of Congress’s
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concern that the EPA focus new
contaminant regulations on priority
health concerns, Congress could not
have intended that the EPA’s regulatory
decision-making be hamstrung by older
data when newer, more accurate
scientific and public health data are
available, especially when those data
demonstrate that regulation of a new
contaminant would not present a
meaningful opportunity for health risk
reduction.
Moreover, the EPA notes that the
statute specifically provides that a
decision not to regulate a contaminant
is a final Agency action subject to
judicial review. SDWA
1412(b)(1)(B)(ii)(IV). Congress could
have—but did not—specify the same
with respect to determinations to
regulate. Congress also did not
explicitly prohibit the EPA from
withdrawing or modifying a regulatory
determination. Congress’ silence with
respect to determinations to regulate
suggests that Congress intended that
such a determination is not itself a final
agency action, but rather a preliminary
step in a decision-making process
culminating in a NPDWR and thus
subject to reconsideration based on new
data and analysis considered during the
36 month promulgation process
specified in the statute. Accordingly,
reconsideration of this preliminary
finding—and withdrawal of the
determination based on subsequent
analysis mandated for NPDWR
development—is fully consistent with
the statutory decision-making
framework.
D. Statutory Framework and Perchlorate
Regulatory History
Section 1412(b)(1)(B)(i) of the SDWA
requires the EPA to publish every five
years a Contaminant Candidate List
(CCL). The CCL is a list of drinking
water contaminants that are known or
anticipated to occur in public water
systems and are not currently subject to
federal drinking water regulations. The
EPA uses the CCL to identify priority
contaminants for regulatory decisionmaking and information collection. The
placement of a substance on the CCL
does not require that it be regulated
under the SDWA. Contaminants listed
on the CCL may require future
regulation under the SDWA. The EPA
included perchlorate on the first,
second, and third CCLs published in
1998 (63 FR 10274, March 2, 1998),
2005 (70 FR 9071, February 24, 2005),
and 2009 (74 FR 51850, October 8,
2009).
The EPA collects data on the CCL
contaminants to better understand their
potential health effects and to determine
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the levels at which they occur in public
water systems. SDWA 1412(b)(1)(B)(ii)
requires that, every five years, the EPA,
after consideration of public comment,
issue a determination of whether or not
to regulate at least five contaminants on
each CCL. For any contaminant that the
EPA determines meets the criteria for
regulation under SDWA 1412(b)(1)(E),
the EPA must propose a NPDWR within
two years and promulgate a final
regulation within 18 months of the
proposal (which may be extended by 9
additional months).
As part of its responsibilities under
the SDWA, the EPA implements section
1445(a)(2) (‘‘Monitoring Program for
Unregulated Contaminants’’). This
section requires that once every five
years, the EPA issue a list of no more
than 30 unregulated contaminants to be
monitored by public water systems.
This monitoring is implemented
through the Unregulated Contaminant
Monitoring Rule (UCMR), which
collects data from community water
systems and non-transient, noncommunity water systems. The first four
UCMRs collected data from a census of
large water systems (serving more than
10,000 people) and from a statistically
representative sample of small water
systems. On September 17, 1999, the
EPA published its first UCMR (64 FR
50556), which required all large systems
and a representative sample of small
systems to monitor for perchlorate and
25 other contaminants (USEPA, 1999).
Water system monitoring data for
perchlorate were collected from 2001 to
2005.
The EPA and other federal agencies
asked the National Research Council
(NRC) to evaluate the health
implications of perchlorate ingestion. In
its 2005 report, the NRC concluded that
perchlorate exposure inhibits the
transport of iodide 1 into the thyroid by
a protein molecule known as the
sodium/iodide symporter (NIS), which
may lead to decreases in the production
of two thyroid hormones, thyroxine (T3)
and triiodothyronine (T4), and increases
in the production of thyroid-stimulating
hormone (TSH) (National Research
Council (NRC), 2005). Additionally, the
NRC concluded that the most sensitive
population to perchlorate exposure are
‘‘the fetuses of pregnant women who
might have hypothyroidism or iodide
deficiency’’ (p. 178). The EPA
established a reference dose (RfD)
consistent with the NRC’s
recommended RfD of 0.7 mg/kg/day for
1 For
the purposes of this document, ‘‘iodine’’
will be used to refer to dietary intake before
entering the body. Once in the body, ‘‘iodide’’ will
be used to refer to the ionic form.
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perchlorate. The reference dose is an
estimate of a human’s daily exposure to
perchlorate that is likely to be without
an appreciable risk of adverse effects.
This RfD was based on a study (Greer,
Goodman, Pleus, & Greer, 2002) of
perchlorate’s inhibition of radioactive
iodine uptake in healthy adults and the
application of an uncertainty factor of
10 for intraspecies variability (USEPA,
2005a).
In October 2008, the EPA published a
preliminary regulatory determination
not to regulate perchlorate in drinking
water and requested public comment
(73 FR 60262, October 10, 2008). In that
preliminary determination, the EPA
found that perchlorate did not occur
with a frequency and at levels of public
health concern within the meaning of
the SDWA, and that development of a
regulation did not present a meaningful
opportunity for health risk reduction for
persons served by public water systems.
In reaching this conclusion, the EPA
derived and used a Health Reference
Level (HRL) of 15 mg/L based on the RfD
of 0.7 mg/kg/day and body weight and
exposure information for pregnant
women (USEPA, 2008a). Using the
UCMR 1 occurrence data, the EPA
estimated that less than 1% of drinking
water systems (serving approximately 1
million people) had perchlorate levels
above the HRL of 15 mg/L. Based on this
information, the EPA found that
perchlorate did not occur at a frequency
and at levels of public health concern.
The EPA also determined there was not
a meaningful opportunity for a NPDWR
for perchlorate to reduce health risks.
In August 2009, the EPA published a
supplemental request for comment with
new analysis that derived potential
alternative Health Reference Levels
(HRLs) for 14 life stages, including
infants and children. The analysis used
the RfD of 0.7 mg/kg/day and life stagespecific bodyweight and exposure
information, resulting in comparable
perchlorate concentrations in drinking
water, based on life stage, of between 1
mg/l to 47 mg/l (74 FR 41883; USEPA,
2009a).
In February 11, 2011, the EPA
published its determination to regulate
perchlorate (76 FR 7762; USEPA, 2011)
after careful consideration of public
comments on the October 2008 and
August 2009 notices. The EPA found at
that time that perchlorate may have an
adverse effect on the health of persons;
that it is known to occur, or that there
is a substantial likelihood that it will
occur, in public drinking water systems
with a frequency and at levels that
present a public health concern; and
that regulation of perchlorate presented
a meaningful opportunity for health risk
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43993
reduction for persons served by public
water systems. The EPA found that as
many as 16 million people could
potentially be exposed to perchlorate at
levels of concern, up from 1 million
people originally estimated in the 2008
notice.
As a result of the determination, and
as required by SDWA 1412(b)(1)(E), the
EPA initiated the process to develop a
MCLG and a NPDWR for perchlorate.
In September 2012, the U.S. Chamber
of Commerce (the Chamber) submitted
to the EPA a Request for Correction
under the Information Quality Act
regarding the EPA’s regulatory
determination.2 In the request, the
Chamber claimed that the UCMR 1 data
used in the EPA’s occurrence analysis
did not comply with data quality
guidelines and were not representative
of current conditions. In response to this
request, the EPA reassessed the data and
removed certain source water samples
that could be paired with appropriate
follow-up samples located at the entry
point to the distribution system. The
EPA also updated the UCMR 1 data in
the analysis for systems in California
and Massachusetts, using state
compliance data to reflect current
occurrence conditions after state
regulatory limits for perchlorate were
implemented. For more information on
the Chamber’s request and the EPA’s
response, see the Perchlorate
Occurrence and Monitoring Report
(USEPA, 2019b).
As required by section 1412(d) of the
SDWA, as part of the NPDWR
development process, the EPA
requested comments from the Science
Advisory Board (SAB) in 2012, seeking
guidance on how best to consider and
interpret the life stage information, the
epidemiologic and biomonitoring data
since the NRC report, physiologicallybased pharmacokinetic (PBPK) analyses,
and the totality of perchlorate health
information to derive an MCLG for
perchlorate. In May 2013, the SAB
recommended that the EPA:
• Derive a perchlorate MCLG that
addresses sensitive life stages through
physiologically-based pharmacokinetic/
pharmacodynamic modeling based
upon its mode of action, rather than the
default MCLG approach using the RfD
and specific chemical exposure
parameters;
• expand the modeling approach to
account for thyroid hormone
perturbations and potential adverse
2 The U.S. Chamber of Commerce letter to the
EPA and other corresponding records are available
at https://www.epa.gov/quality/epa-informationquality-guidelines-requests-correction-and-requestsreconsideration#12004.
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neurodevelopmental outcomes from
perchlorate exposure;
• utilize a mode-of-action framework
for developing the MCLG that links the
steps in the proposed mechanism
leading from perchlorate exposure
through iodide uptake inhibition—to
thyroid hormone changes—and finally
to neurodevelopmental impacts; and
• ‘‘[e]xtend the [BBDR] model
expeditiously to . . . provide a key tool
for linking early events with subsequent
events as reported in the scientific and
clinical literature on iodide deficiency,
changes in thyroid hormone levels, and
their relationship to
neurodevelopmental outcomes during
sensitive early life stages’’(SAB for the
U.S. EPA, 2013, p. 19).
To address the SAB
recommendations, the EPA revised an
existing PBPK/PD model that describes
the dynamics of perchlorate, iodide, and
thyroid hormones in a woman during
the third trimester of pregnancy
(Lumen, Mattie, & Fisher, 2013; USEPA,
2009b). The EPA also created its own
Biologically Based Dose Response
(BBDR) models that included the
additional sensitive life stages identified
by the SAB, i.e., breast- and bottle-fed
neonates and infants (SAB for the U.S.
EPA, 2013, p. 19).
To determine whether the Agency had
implemented the SAB recommendations
for modeling thyroid hormone changes,
the EPA convened an independent peer
review panel to evaluate the BBDR
models in January 2017 (External Peer
Reviewers for USEPA, 2017). The EPA
considered the recommendations from
the 2017 peer review and made
necessary model revisions to increase
the scientific rigor of the model and the
modeling results, including extending
the BBDR model to the first trimester
and incorporating the TSH feedback
mechanism.
The EPA convened a second
independent peer review panel in
January 2018 to evaluate the revisions to
the BBDR model, including the
transition from the third to the first
trimester as the life stage of interest. The
EPA also presented several approaches
to link the thyroid hormone changes in
a pregnant mother predicted by the
BBDR model to neurodevelopmental
effects using evidence from the
epidemiological literature (External Peer
Review for U.S. EPA, 2018).
In response to a lawsuit brought to
enforce the deadlines in SDWA
1412(b)(1)(E) triggered by the 2011
regulatory determination for
perchlorate, on October 18, 2016, the
U.S. District Court for the Southern
District of New York entered a consent
decree, requiring the EPA to sign for
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publication a proposal for a MCLG and
NPDWR for perchlorate in drinking
water no later than October 31, 2018,
and to sign for publication a final MCLG
and NPDWR for perchlorate in drinking
water no later than December 19, 2019.
The deadline for the EPA to propose a
MCLG and NPDWR for perchlorate in
drinking water was later extended to
May 28, 2019, and the date for signature
of a final MCLG and NPDWR was
extended to no later than June 19, 2020.
The consent decree is available in the
docket for this action.
In compliance with the deadline
established in the consent decree, on
May 23, 2019, the EPA Administrator
signed a proposed rulemaking
document seeking public comment on a
range of options regarding the regulation
of perchlorate in public drinking water
systems. The proposed rulemaking
document was published in the Federal
Register on June 26, 2019. 84 FR 30524.
The EPA proposed a NPDWR for
perchlorate with an MCL and MCLG of
56 mg/L. The proposed MCLG of 56 mg/
L was based on avoiding an estimated
2 point IQ decrement associated with
exposure to perchlorate in drinking
water during the most sensitive life
stage (the fetus) within a specific
segment of the population (iodine
deficient pregnant women).
The EPA also requested comment on
two alternative MCL/MCLG values of 18
mg/L and 90 mg/L. These alternatives
were based upon avoiding an estimated
1 point and 3 point IQ decrement
respectively, associated with
perchlorate exposure. Additionally, the
EPA requested comment on whether the
2011 regulatory determination should
be withdrawn, based on new
information including updated
occurrence data on perchlorate in
drinking water and new analysis of the
concentration of perchlorate in drinking
water that represents a level of health
concern.
III. Withdrawal of the 2011 Regulatory
Determination and Final Determination
Not To Regulate Perchlorate
In determining whether to regulate a
particular contaminant, the EPA must
follow the criteria mandated by the 1996
SDWA Amendments. Specifically, in
order to issue a MCLG and NPDWR for
perchlorate, the EPA must determine
that perchlorate ‘‘may have an adverse
effect on the health of persons,’’ that
perchlorate occurs at ‘‘a frequency and
at levels of public health concern’’ in
public water systems, and that
regulation of perchlorate in drinking
water systems ‘‘presents a meaningful
opportunity for health risk reduction for
persons served by public water
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systems.’’ SDWA 1412(b)(1)(A). In
preparing the 2019 proposal for
perchlorate, the EPA updated and
improved information on the levels of
public health concern and the frequency
and levels of perchlorate in public water
systems. The following is the EPA’s
reassessment of the regulatory
determination criteria applied to the
best available health science and
occurrence data for perchlorate.
A. May perchlorate have an adverse
effect on the health of persons?
Yes, perchlorate may have adverse
health effects above certain exposure
levels. The perchlorate anion is
biologically significant specifically with
respect to the functioning of the thyroid
gland. Above certain exposure levels,
perchlorate can interfere with the
normal functioning of the thyroid gland
by inhibiting the transport of iodide into
the thyroid, resulting in a deficiency of
iodide in the thyroid. Perchlorate
inhibits (or blocks) iodide transport into
the thyroid by chemically competing
with iodide, which has a similar shape
and electric charge. The transfer of
iodide from the blood into the thyroid
is an essential step in the synthesis of
thyroid hormones. Thyroid hormones
play an important role in the regulation
of metabolic processes throughout the
body and are also critical to developing
fetuses and infants, especially for brain
development. Because the developing
fetus depends on an adequate supply of
maternal thyroid hormones for its
central nervous system development
during the first and second trimester of
pregnancy, iodide uptake inhibition
from perchlorate exposure has been
identified as a concern in connection
with increasing risk of
neurodevelopmental impairment in
fetuses of pregnant women with low
dietary iodine. Poor iodide uptake and
subsequent impairment of the thyroid
function in pregnant and lactating
women have been linked to delayed
development and decreased learning
capability in their infants and children
(NRC, 2005). There is scientific
evidence to support that perchlorate can
reduce iodide uptake and therefore alter
the level of thyroid hormones. There is
also scientific evidence that changes in
thyroid hormone levels in a pregnant
woman may be linked to changes in the
neurodevelopment of her offspring. The
existence of a quantifiable relationship
between thyroid hormone changes and
neurodevelopmental outcomes has
strong support from the literature on the
subject; however, not every study
identifies an association between
maternal thyroid hormone levels and
the neurodevelopmental outcomes and
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the state of the science on this
relationship is constantly evolving.
Therefore, the EPA continues to find
that perchlorate may have an adverse
effect on the health of persons above
certain exposure levels based on its
ability to interfere with thyroid
hormone production.
B. Is perchlorate known to occur or is
there a substantial likelihood that
perchlorate will occur in public water
systems with a frequency and at levels
of public health concern?
The EPA has determined that
perchlorate does not occur with a
frequency and at levels of public health
concern in public water systems. The
EPA has made this determination by
comparing the best available data on the
occurrence of perchlorate in public
water systems with potential MCLGs for
perchlorate.
In past regulatory determinations, the
EPA has identified HRLs as benchmarks
against which the EPA compares the
concentration of a contaminant found in
public water systems to determine
whether it occurs at levels of public
health concern. For the 2011 regulatory
determination, the EPA identified
potential alternative HRL values ranging
from 1 to 47 mg/L for 14 different life
stages. These HRLs were not final
decisions about the level of perchlorate
in drinking water that is without
adverse effects. For the 2019 proposal,
the EPA derived three potential MCLGs
for perchlorate of 18, 56, and 90 mg/L for
the most sensitive life stage using the
best available peer reviewed science in
accordance with the SDWA. After
considering public comment, the EPA
used these potential MCLGs as the
levels of public health concern in
assessing the frequency of occurrence of
perchlorate in this regulatory
determination. These MCLGs were set at
levels to avoid estimated IQ decrements
of 1, 2, and 3 points respectively in the
most sensitive life stage, the children of
hypothyroxinemic women with low
iodine intake. The EPA proposed an
MCLG of 56 mg/L and alternative MCLG
values of 18 and 90 mg/L.
The rationale used in deriving the
numerical values is presented in greater
detail in the EPA technical support
document entitled ‘‘Deriving a
Maximum Contaminant Level Goal for
Perchlorate in Drinking Water’’ (USEPA,
2019a).
The EPA compared these potential
MCLG values with the updated
perchlorate UCMR 1 occurrence data
set. A comprehensive description of the
perchlorate occurrence data is presented
in Section VI of the 2019 proposal. It is
also available in the ‘‘Perchlorate
Occurrence and Monitoring Report’’
(USEPA, 2019a).
The occurrence data for perchlorate
were collected from 3,865 PWSs
between 2001 and 2005 under the
UCMR 1. In the 2019 proposal, the EPA
modified the UCMR 1 data set in
response to concerns raised by
stakeholders regarding the data quality
and to represent current conditions in
California and Massachusetts, which
have enacted perchlorate regulations
since the UCMR 1 data were collected.
Massachusetts promulgated a drinking
water standard for perchlorate of 2 mg/
L in 2006 (MassDEP, 2006), and
California promulgated a drinking water
standard of 6 mg/L in 2007 (California
Department of Public Health, 2007).
Systems in these states are now required
to keep perchlorate levels in drinking
water below their state limits. As
discussed below, the EPA finds that
perchlorate levels in drinking water and
sources of drinking water have
decreased since the UCMR 1 data
collection. The main factors
43995
contributing to the decrease in
perchlorate levels are the promulgation
of drinking water regulations for
perchlorate in California and
Massachusetts and the ongoing
remediation efforts in the state of
Nevada to address perchlorate
contamination in groundwater adjacent
to the lower Colorado River upstream of
Lake Mead.
To update the occurrence data for
systems sampled during UCMR 1 from
California and Massachusetts, the EPA
identified all systems and
corresponding entry points which had
reported perchlorate detections in
UCMR 1. Once the systems and entry
points with detections were
appropriately identified, the EPA then
used publicly available California and
Massachusetts monitoring data for
perchlorate, to replace the original
UCMR1 data with more recent data
where available (Perchlorate Occurrence
and Monitoring Report, USEPA, 2019b).
The EPA has determined that the
UCMR 1 data with these updates are the
best available data collected in
accordance with accepted methods
regarding the frequency and level of
perchlorate nationally. The UCMR 1
data are from a census of the large water
systems (serving more than 10,000
people) and a statistically representative
sample of small water systems that
provides the best available, national
assessment of perchlorate occurrence in
drinking water.
The EPA used entry point maximum
measurements to estimate potential
baseline occurrence and exposure at
levels that exceed the potential MCLG
thresholds. The maximum
measurements indicate highest
perchlorate levels reported in at least
one quarterly sample from surface water
systems and at least one semi-annual
sample from ground water systems.
TABLE 1—PERCHLORATE OCCURRENCE AND EXPOSURE (UPDATED UCMR 1 DATA SET)
Entry points
with detections
above threshold
Threshold concentration (μg/L)
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18 μg/L .....................................................................................
56 μg/L .....................................................................................
90 μg/L .....................................................................................
Table 1 presents the number and
percentage of water systems that
reported perchlorate at levels exceeding
the three proposed MCLG threshold
concentrations. In summary, the
updated perchlorate occurrence
information suggests that at an MCLG of
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Water systems
with detections
above threshold
17
2
1
15
2
1
18 mg/L, there would be 15 systems
(0.03% of all water systems in the U.S.)
that would exceed the threshold, at an
MCLG of 56 mg/L, two systems (0.004%
of all water systems in the U.S.) would
exceed the threshold, and finally one
system would exceed the MCLG
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Percent of U.S.
water systems
with detections
above threshold
(percent)
0.03
0.004
0.002
Population
served
620,560
32,432
25,972
threshold of 90 mg/L. Based on the
analysis of drinking water occurrence
presented in the 2019 proposal and the
data summarized in Table 1 and the
range of potential MCLGs, the EPA
concludes that perchlorate does not
occur with a frequency and at levels of
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public health concern in public water
systems.
The EPA notes that in 2008, the EPA
stated in its preliminary regulatory
determination that perchlorate did not
occur with a frequency and at levels of
public health concern in public water
systems based upon the health effects
and occurrence information available at
that time, which indicated that 0.8% of
public water system had perchlorate at
levels exceeding the HRL of 15 mg/L.
The EPA also stated that there was not
a meaningful opportunity for a NPDWR
to reduce health risks based upon the
estimates at that time that 0.9 million
people had perchlorate levels above the
HRL. The EPA further notes that the
Agency has previously determined
CCL1 and CCL2 contaminants did not
occur with frequency at levels of public
health concern when the percentage of
water systems exceeding the HRL were
greater than the frequency of perchlorate
occurrence level at the proposed MCL
(0.004% of all water systems in the
U.S.). For example, in 2003 the EPA
determined that aldrin did not occur
with a frequency and at levels of public
health concern based upon data that
showed 0.2% of water systems had
aldrin at levels greater than the HRL.
The EPA also concluded that there was
not a meaningful opportunity for health
risk reduction for persons served
through a drinking water regulation
based on this occurrence data and the
estimate that these systems above the
HRL served approximately 1 million
people (USEPA, 2003). In 2008 the EPA
determined that DCPA Mono- and DiAcid degradates did not occur with a
frequency and at levels of public health
concern based on data that showed
0.03% of water systems exceeded the
HRL. The EPA also concluded that there
was not a meaningful opportunity for
health risk reduction through a drinking
water regulation based on this
occurrence data and the estimate that
these systems above the HRL served
approximately 100,000 people (USEPA,
2008b).
While the EPA has made its
conclusion that perchlorate does not
occur at a frequency and at levels of
public health concern in public water
systems based on the updated UCMR 1
data in Table 1 above, the EPA also
sought to find additional information
about the perchlorate levels at the 15
water systems that had at least one
reported result greater than 18 mg/L in
the updated UCMR 1 data. The EPA
found that perchlorate levels have been
reduced at many of these water systems.
Although these water systems were not
required to take actions to reduce
perchlorate in drinking water, many had
conducted additional monitoring for
perchlorate and found decreased levels
or had taken mitigation efforts to
address perchlorate, confirming the
EPA’s conclusion described above. The
status of each of these systems is
described in Table 2 below and
confirms the Agency’s conclusion that is
based upon the information in Table 1.
TABLE 2—UPDATE ON SYSTEMS WITH PERCHLORATE LEVELS ABOVE 18 μg/L IN THE UCMR 1
State
System name
Range of UCMR 1 results
(μg/L) **
Update on mitigation and levels of perchlorate ++
Florida ..................................
Sebring Water ...................
ND–70 ...............................
Florida ..................................
Manatee County Utilities
Dept.
ND–30 ...............................
Georgia ................................
Oconee Co.—Watkinsville
38 (single sample) .............
Louisiana .............................
St. Charles Water District 1
East Bank.
City of Aberdeen ...............
ND–24 ...............................
Chapel Hill—Aberdeen
Proving Grounds.
ND–20 ...............................
The EPA contacted the Sebring system in January
2020. Operations personnel indicated that no followup/updated monitoring data for perchlorate are
available.
Researchers contacted the system to identify the
source of perchlorate. System personnel attributed
the sole perchlorate detection under UCMR 1 to analytical error. System personnel indicated that three
other quarterly samples collected under UCMR 1 as
well as other subsequent perchlorate sampling efforts were non-detect. Source: AWWA (2008).
Researchers contacted the system and found that a
perchlorate contaminated well was removed from
service in 2003. The system indicates that perchlorate is no longer detected. Source: Luis et al.
(2019).
The EPA was not able to identify updated data on perchlorate levels for this system.
The system’s 2018 Consumer Confidence Report
(CCR) indicates that perchlorate was not detected.
According to the Maryland Department of Environment, perchlorate was not detected in this system in
2019. In addition, researchers contacted the system
and found that there has been no detection of perchlorate since treatment was installed in 2009.
Source: Luis et al. (2019).
The EPA contacted the Chapel Hill System in January
2020. Water system personnel indicate that the
Chapel Hill WTP was taken off-line and was replaced with a new treatment plant and five new production wells. The new treatment plant started operations on January 27, 2020. System personnel also
indicate that monitoring was conducted in November
2019 and perchlorate was not detected in either the
source well water or the finished water. In addition,
according to the Maryland Department of Environment, perchlorate was not detected in this system in
2019.
Maryland ..............................
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Maryland ..............................
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43997
TABLE 2—UPDATE ON SYSTEMS WITH PERCHLORATE LEVELS ABOVE 18 μg/L IN THE UCMR 1—Continued
State
System name
Range of UCMR 1 results
(μg/L) **
Update on mitigation and levels of perchlorate ++
Mississippi ...........................
Hilldale Water District ........
ND–20 ...............................
New Mexico .........................
Deming Municipal Water
System.
15–20 .................................
Nevada ................................
City of Henderson .............
6–23 ...................................
Ohio .....................................
Fairfield City PWS .............
6–27 ...................................
Ohio .....................................
Hecla Water Association—
Plant PWS.
ND–32 ...............................
Oklahoma ............................
Enid ...................................
ND–30 ...............................
Pennsylvania .......................
Meadville Area Water Authority.
ND–33 ...............................
Puerto Rico ..........................
Utuado Urbano ..................
ND–420 .............................
Texas ...................................
City of Levelland ................
ND–32 ...............................
The EPA contacted the Hilldale System in January
2020. Water system personnel indicated that no follow-up/updated monitoring data for perchlorate are
available.
Data from the EPA’s SDWIS/FED database indicates
that the entry point that reported detections in
UCMR 1 (Well #3) is now inactive (i.e., the contaminated source is no longer in use).
Researchers report that the perchlorate levels described in the system’s CCR ranged from non-detect to 9.7 μg/L. Source: AWWA (2008).
The EPA contacted the Fairfield City System in January 2020. Water system personnel indicated that follow-up monitoring was conducted after UCMR 1,
between 2002 and 2004. The Ohio EPA provided
copies of the follow-up monitoring results which indicate that results at the entry point ranged from nondetect to 13 μg/L.
The EPA contacted the Hecla Water Association System in January 2020. Water system personnel indicated that that no follow-up/updated monitoring data
for perchlorate are available.
The EPA reviewed Oklahoma’s monitoring data and
did not find any monitoring results reported for perchlorate.
The EPA contacted the Meadville System in January
2020. Water system personnel indicated that no follow-up/updated monitoring data for perchlorate are
available.
The EPA contacted the Puerto Rico Aqueduct and
Sewer Authority (PRASA) in January 2019. PRASA
personnel indicated that no updated monitoring data
for perchlorate are available. NOTE: The PRASA
personnel stated that the Utuado water system was
significantly impacted by Hurricane Maria and that
monitoring records from years prior to 2017 were
lost.
Researchers found that a water storage tank was the
source of perchlorate contamination. The wells feeding the tank were tested by the state and perchlorate was not detected. The water tank was shut
off from service. Source: Luis et al. (2019).
**Values have been rounded. ND describes a sampling event where perchlorate was not detected at or above the UCMR 1 minimum reporting
level of 4 μg/L. UCMR 1 results collected between 2001 and 2005.
++To obtain updated data and/or information regarding perchlorate levels, the EPA reviewed Consumer Confidence Reports and other publicly
available data, as well as published studies. In addition, the EPA contacted some water systems for information about current perchlorate levels.
(USEPA, 2020a)
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C. Is there a meaningful opportunity for
the reduction of health risks from
perchlorate for persons served by public
water systems?
The EPA’s analysis presented in the
2019 proposal demonstrates that a
NPDWR for perchlorate does not present
a meaningful opportunity for health risk
reduction for persons served by public
water systems. As discussed above, the
EPA found that perchlorate occurs with
very low frequency at levels of public
health concern. Based on updated
UCMR 1 occurrence information, there
were 15 water systems (0.03% of all
water systems in the U.S.) that detected
perchlorate in drinking water above the
lowest proposed alternative MCLG of 18
mg/L, and only 1 system had a detection
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above the proposed alternative MCLG of
90 mg/L. Specifically, Table 1 presents
the population served by PWSs that
were monitored under UCMR 1 for
which the highest reported perchlorate
concentration was greater than the
identified thresholds. The EPA
estimates 3 that the number of people
who may be potentially consuming
water containing perchlorate at levels
3 The values shown in Table 1 are based on the
revised UCMR 1 data. The EPA also applied
statistical sampling weights to the small systems
results to extrapolate to national results. There was
one small system included in the statistical sample
stratum which had a perchlorate measurement
exceeding 18 mg/L. Accordingly, the EPA estimates
that approximately 41,000 small system customers
may be exposed to perchlorate greater than
18 mg/L.
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that could exceed the levels of concern
for perchlorate could range between
26,000 and 620,000.
The small number of water systems
with perchlorate levels greater than
identified thresholds, and the
correspondingly small population
served, provides ample support for the
EPA’s conclusion that the regulation of
perchlorate does not present a
‘‘meaningful opportunity for health risk
reduction for persons served by public
water systems,’’ within the meaning of
SDWA 1412(b)(1)(A)(iii).
While the EPA does not believe that
a national primary drinking water
regulation presents a meaningful
opportunity for health risk reduction,
the Agency remains committed to
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working with States and communities in
addressing perchlorate contamination of
drinking water. For example, the EPA
has issued a document entitled
‘‘Perchlorate Recommendations for
Public Water Systems’’ which provides
recommendations for actions that
systems may take if there are concerns
about perchlorate (USEPA, 2020b). The
document outlines steps public systems
can take to address perchlorate in
drinking water, including testing,
installing treatment equipment, and
communication with customers.
Although a cost benefit analysis is not
one of the three SDWA criteria for
making a regulatory determination, the
EPA also considered the findings of the
Health Risk Reduction and Cost
Analysis (HRRCA, USEPA 2019c) as
additional information confirming the
appropriateness of the withdrawal of the
regulatory determination. The HRRCA
for perchlorate (which was presented in
the 2019 proposal) provides a unique set
of economic data indicators that are not
available for regulatory determinations
because the HRRCA is required for a
proposed NPDWR under SDWA
1412(b)(3)(C), but is not required to
support a regulatory determination.
Accordingly, because the EPA initially
determined that perchlorate met the
criteria for regulation and began the
regulatory analysis process, the HRRCA
was available with respect to
perchlorate at this stage in the SDWA
process, and the Agency considered this
comprehensive economic analysis in
informing its decision to withdraw the
regulatory determination.
Specifically, the HRRCA provides a
description of the potential benefits and
costs of a drinking water regulation for
perchlorate. For all potential regulatory
levels considered for perchlorate (18,
56, and 90 mg/L), the total costs
associated with establishing a regulation
(ranging from $9.5 to $18.0 million
across discount rates and levels) were
substantially higher than the potential
range of benefits (ranging from $0.3 to
$3.7 million) (USEPA, 2019c). The
infrequent occurrence of perchlorate at
levels of health concern imposes high
monitoring and administrative cost
burdens on public water systems and
the states, while having little impact on
health risk reductions and the
associated low estimates of benefits. The
EPA is not finalizing the HRRCA for this
final action nor is the EPA conducting
an analysis in accordance with the
Regulatory Flexibility Act because the
Agency is not promulgating a final
regulation.
Based on a comparison of costs and
benefits estimated at the three potential
regulatory levels, the EPA determined in
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the 2019 proposal that the benefits of
establishing a drinking water regulation
for perchlorate do not justify the
potential costs.
A drinking water regulation for
perchlorate would impose significant
burdens on states and water systems,
mainly associated with requirements for
monitoring, including initial monitoring
and long-term monitoring for over
60,000 systems (see Section VIII of the
2019 proposal for more information),
but would result in very few systems
having to take action to reduce
perchlorate levels. It is of paramount
importance that water systems
(particularly medium, small, and
economically distressed systems) focus
their limited resources on actions that
ensure compliance with existing
NPDWRs and maintain their technical,
managerial, and financial capacity to
improve system operations and the
quality of water being provided to their
customers, rather than spending
resources monitoring for contaminants
that are unlikely to occur.
D. What is the EPA’s final regulatory
determination on perchlorate?
Based on the EPA’s analysis of the
best available public health information,
and after careful review and
consideration of public comments on
the June 2019 proposal, the Agency is
withdrawing its 2011 determination and
is making a final determination not to
regulate perchlorate. Accordingly, the
EPA will not issue a NPDWR for
perchlorate at this time. While the EPA
has found that perchlorate may have an
adverse effect on human health above
certain exposure levels, based on the
analysis presented in this document and
supporting record, the EPA has
determined that perchlorate does not
occur in public water systems with a
frequency and at levels of public health
concern and that regulation of
perchlorate does not present a
meaningful opportunity to reduce
health risks for persons served by public
water systems. This conclusion is based
on the best available peer reviewed
science and data collected in
accordance with accepted methods on
perchlorate health effects and
occurrence.
IV. Summary of Key Public Comments
on Perchlorate
The EPA received approximately
1,500 comments from individuals or
organizations on the June 2019
proposal. This section briefly discusses
the key technical issues raised by
commenters and the EPA’s response.
Comments are also addressed in the
‘‘Comment Response Document for the
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Final Regulatory Action for Perchlorate’’
(USEPA, 2020c) available at https://
www.regulations.gov (Docket ID No.
EPA–HQ–OW–2018–0780).
A. SDWA Statutory Requirements and
the EPA’s Authority
The EPA received comments stating
that the Agency should promulgate an
MCLG and MCL for perchlorate and
comments stating that the Agency
should not promulgate a regulation.
After considering these comments, the
EPA has re-evaluated perchlorate in
accordance with SDWA 1412(b)(1)(A),
which requires that the Agency
promulgate a NPDWR if (i) the
contaminant may have an adverse effect
on the health of persons; (ii) the
contaminant is known to occur or there
is a substantial likelihood that the
contaminant will occur in public water
systems with a frequency and at levels
of public health concern; and (iii) in the
sole judgment of the Administrator,
regulation of such contaminant presents
a meaningful opportunity for health risk
reduction for persons served by public
water systems.
The EPA has determined, based upon
the best available peer reviewed science
and data collected in accordance with
accepted methods, that perchlorate does
not occur at a frequency and at levels of
public health concern, and that
regulation of perchlorate does not
present a meaningful opportunity for
health risk reduction. Because
perchlorate does not meet the statutory
criteria for regulation, the EPA lacks the
authority to issue a MCLG or NPDWR
for perchlorate, and, is therefore
withdrawing its 2011 regulatory
determination and issuing this final
determination not to regulate
perchlorate. For more information
regarding the EPA’s statutory authority
to withdraw its regulatory
determination, see Section II.C above.
B. Health Effects Assessment
Health Effects/MCLG Derivation
The EPA received comments
indicating that the Agency should
utilize different approaches to derive
the MCLG for perchlorate including
approaches that some states used to
develop their perchlorate advisory
levels or drinking water standards. The
EPA considered a number of alternative
approaches to develop the MCLG for
perchlorate and in accordance with
SDWA 1412(e), the Agency sought
recommendations from the Science
Advisory Board. The EPA derived the
proposed MCLG for perchlorate based
on the approach recommended by the
Science Advisory Board (SAB) (SAB for
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the U.S. EPA, 2013). The SAB
recommended that ‘‘the EPA derive a
perchlorate MCLG that addresses
sensitive life stages through
physiologically-based pharmacokinetic/
pharmacodynamic modeling based
upon its mode of action rather than the
default MCLG approach using the RfD
and specific chemical exposure
parameters.’’ The EPA has implemented
these recommendations and has
obtained two independent peer reviews
of the analysis. These peer reviewers
stated that: ‘‘[o]verall, the panel agreed
that the EPA and its collaborators have
prepared a highly innovative state-ofthe-science set of quantitative tools to
evaluate neurodevelopmental effects
that could arise from drinking water
exposure to perchlorate. While there is
always room for improvement of the
models, with limited additional work to
address the committee’s comments
below, the current models are fit-forpurpose to determine an MCLG’’
(External Peer Reviewers for USEPA,
2018, p. 2).
The EPA received comments
indicating that the most sensitive life
stages were not selected and/or
considered in the Agency’s approach.
The EPA disagrees. Gestational
exposure to perchlorate during
neurodevelopment is the most sensitive
time period. The NRC concluded that
the population most sensitive to
perchlorate exposure are ‘‘the fetuses of
pregnant women who might have
hypothyroidism or iodide deficiency’’
(p. 178, NRC 2005). In addition, there is
clear evidence that disrupted maternal
thyroid hormone levels during gestation
can impact neurodevelopment later in
life (Alexander et al., 2017; Costeira et
al., 2011; Endendijk et al., 2017;
Ghassabian, Bongers-Schokking,
Henrichs, Jaddoe, & Visser, 2011;
Glinoer & Delange, 2000; Glinoer &
Rovet, 2009; Gyllenberg et al., 2016;
Henrichs et al., 2010; Korevaar et al.,
2016; Morreale de Escobar, Obrego´n, &
Escobar del Rey, 2004; Noten et al.,
2015; Pop et al., 2003, 1999; SAB for the
U.S. EPA, 2013; Thompson et al., 2018;
van Mil et al., 2012; Wang et al., 2016;
Zoeller & Rovet, 2004; Zoeller et al.,
2007). The available data demonstrate
that the fetus of the first trimester
pregnant mother, when compared to
other life-stages, experiences the
greatest impact from the same dose of
perchlorate, which is described in detail
in Section 6 of the document ‘‘Deriving
a Maximum Contaminant Level Goal for
Perchlorate in Drinking Water’’ (USEPA,
2019a). Some commenters suggested
that the bottle-fed infant is a more
sensitive life-stage. The EPA disagrees.
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As described in the January 2017 Peer
Review Report on the original
Biologically Based Dose Response
(BBDR) model, the bottle-fed infant’s
thyroid hormone levels were not
impacted by doses of perchlorate up to
20 mg/day (External Peer Reviewers for
USEPA, 2017). This lack of any impact
is due primarily to the iodine in the
formula, which offsets the impact of
perchlorate on the thyroid.
The EPA received comments
advocating for the use of the populationbased approach evaluating the shift in
the proportion of a population that
would fall below a hypothyroxinemic
cut point under a perchlorate exposure
scenario. The EPA chose to develop the
MCLG using dose-response functions
from the epidemiological literature to
estimate neurodevelopmental impacts
in the offspring of pregnant women
exposed to perchlorate. The EPA
selected this proposed approach
because it is consistent with the
SDWA’s definition of a MCLG to avoid
adverse health effects and because it is
most consistent with the SAB
recommendations. In addition, given
that thyroid hormone levels vary by
reference population and that there is
not a defined threshold for the
concentration of fT4 representing
hypothyroxinemia makes the
population-based approach less
desirable than the approach selected
(USEPA, 2018).
End Point Selection/Basis
The EPA received comments
regarding the magnitude of an IQ change
which should be used in deriving the
MCLG. The EPA’s proposed MCLG was
based upon avoiding a 2% change in IQ
in the most sensitive life stage, and the
EPA also requested comment on
alternative options for the MCLG that
would respectively avoid 1% or 3%
change in IQ in the most sensitive life
stage. Many comments stated that the
EPA should at most consider a 1% IQ
change. However, several commenters
stated that a 3% change is too small to
have a meaningful impact and suggested
that the EPA consider a higher IQ
percent change.
The EPA uses a variety of science
policy approaches to select points of
departure for developing regulatory
values. For instance, in noncancer risk
assessment, the EPA often uses a
percentage change in value. When
assessing toxicological data, a 10% extra
risk (for discrete data), or a 1 standard
deviation (i.e., 15 IQ points) change
from the mean (for continuous data) is
often used (USEPA, 2012). A smaller
response to inform a POD has been
applied when using epidemiological
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literature, because there is an inherently
more direct relationship between the
study results and the exposure context
and health endpoint.
Given the difficulty in identifying a
response below which no adverse
impact occurs when considering a
continuous outcome in the human
population, the EPA looked to its
Benchmark Dose Guidance (2012) for
insight regarding a starting point.
Specifically, ‘‘[a] BMR of 1% has
typically been used for quantal human
data from epidemiology studies’’ (p. 21,
USEPA, 2012). For the specific context
of setting an MCLG for perchlorate, the
EPA evaluated the level of perchlorate
in water associated with a 1% decrease,
a 2% decrease, and a 3 percent decrease
in the mean population IQ (i.e., 1, 2 and
3 IQ points).
In evaluating the frequency and level
of occurrence of perchlorate in drinking
water, the EPA has found that
perchlorate does not occur with
frequency even at the lowest alternative
MCLG of 18 mg/L, which is based upon
avoiding a 1% change in IQ in the most
sensitive life stage.
The EPA received comments that the
proposed MCLG did not incorporate an
adequate margin of safety to comply
with the SDWA. The EPA disagrees that
it failed to use an adequate margin of
safety. The EPA’s assessment focused
upon the most sensitive subset of the
population, specifically offspring whose
mothers had low (75 mg/day) iodine
intake and were hypothyroxinemic (fT4
in the lowest 10th percentile of the
population). In addition, to account for
uncertainties and to ensure that the
most sensitive subset of the population
is protected with an adequate margin of
safety, a 3-fold uncertainty factor was
applied to the proposed MCLG
calculation (USEPA, 2019a). More
discussion on the uncertainty factor is
presented below, in the section entitled
‘‘Consideration of Uncertainties.’’
The EPA received some comments
stating that the selection of the study for
informing the relationship between
maternal hormone levels (fT4) and IQ
was inadequately described. Other
comments supported the EPA’s study
selection. The EPA concludes that
selection of the Korevaar et al. (2016)
study is appropriate because that study
provides the most robust data available
with a clear measure of
neurodevelopment that can be
expressed as a function of changing
maternal fT4 exposure, which is
necessary to the development of the
model.
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BBDR and PBPK Models
The EPA received comments
indicating that the BBDR model was not
transparent, scientifically valid, or
based on robust data. The EPA
disagrees. The model represents the best
available peer reviewed science and
uses the best available data to inform a
MCLG for perchlorate. The EPA
disagrees with the suggestion that there
is a significant lack of transparency with
respect to the assumptions related to the
BBDR model. Appendix A of the EPA’s
Proposed MCLG Approaches report
outlines the justification for all
assumptions used in the development of
the BBDR model (USEPA, 2019a). The
EPA also disagrees with the assertion
that the BBDR model is far too uncertain
to be relied upon as the basis for the
derivation of the RfD. The EPA has used
the best available science to calibrate
the pharmacokinetic aspects of the
BBDR model. The development of the
BBDR model was in response to SAB
recommendations, and a model was
deemed to be a more refined approach
to estimating a dose-response
relationship between perchlorate
exposure and maternal fT4 than
anything that was available in the
current scientific literature. The EPA
disputes the claim that the BBDR model
is not scientifically valid, as the Agency
conducted a peer review of the
approach proposed and the reviewers
concluded that the approach was ‘‘fit for
purpose’’ to inform a MCLG for
perchlorate (External Peer Reviewers for
U.S. EPA, 2018, p. 2).
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Consideration of Uncertainties
The EPA received comments on the
Agency’s use of Uncertainty factors
(UFs); with most commenters suggesting
that the EPA should consider a higher
UF for inter-individual variability. The
EPA thoroughly considered the
application of UFs when deriving the
RfDs and followed guidance presented
in ‘‘A review of the reference dose and
reference concentration processes’’
(USEPA, 2002). The EPA concluded that
the UFs are adequately justified, and
subsequently no changes have been
made. Justification for each of the UFs
can be found in Section 11 of the
Agency’s MCLG Derivation report
(USEPA, 2019a).
The EPA selected a UF of 3 for interindividual variability, because the
Agency specifically modeled groups
within the population that are identified
as likely to be at greater risk of the
adverse effects from perchlorate in
drinking water (i.e., the fetus of the
iodide deficient pregnant mother). The
EPA selected model parameters to
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account for the most sensitive
individuals in that group (i.e., muted
TSH feedback, low fT4 values, lowiodine intake). As discussed in the
MCLG Derivation report, the EPA has
attempted to select the most appropriate
inputs to protect the most sensitive
population with an adequate margin of
safety (USEPA, 2019a). The EPA has
determined that the selection of a UF of
3 for inter-individual variability is
justified. As described in the MCLG
Derivation report, because the output
from the BBDR model is specific to the
sensitive population, the EPA
concluded that the UF of 3 is
appropriate. In regard to variation in
sensitivity among the members of the
human population (i.e., inter-individual
variability), section 4.4.5.3 of the EPA
guidance ‘‘A review of the reference
dose and reference concentration
process’’ (USEPA, 2002) document
states, ‘‘In general, the Technical Panel
reaffirms the importance of this UF,
recommending that reduction of the
intraspecies UF from a default of 10 be
considered only if data are sufficiently
representative of the exposure/doseresponse data for the most susceptible
subpopulation(s). Similar to the
interspecies UF, the intraspecies UF can
be considered to consist of both a
toxicokinetic and toxicodynamic
portion (i.e. 10∧0.5 each)’’ (USEPA,
2002). Given that the BBDR model
significantly accounts for differences
within the human population, the full
UF of 10 is not warranted.
One commenter suggested using a UF
greater than 1 to account for the
extrapolation of the lowest-observed
adverse effect level (LOAEL) to the noobserved-adverse-effect-level (NOAEL).
LOAELs and NOAELs were not
identified or used by the EPA in its
assessment because the Agency
employed a sophisticated BBDR
modeling approach, which was coupled
with extrapolation to changes in IQ
using linear regression, to determine a
POD that would not be expected to
represent an adverse effect. Therefore, a
UF of 1 is appropriate. Other
commenters suggested incorporating
UFs for database deficiencies. Based on
the findings of the NRC report, the EPA
has previously concluded that this UF
was not needed for deficiencies in the
perchlorate database (NRC, 2005;
USEPA, 2005a). The EPA determined
that a UF of 1 to account for database
deficiencies is still appropriate, given
that the comprehensiveness of the
perchlorate database has only increased
since 2005.
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Health Advisory
Several commenters suggest that the
EPA should withdraw the 2011
determination to regulate perchlorate
and instead issue an updated health
advisory for perchlorate. The EPA
issued an interim health advisory level
for perchlorate in 2008. Health
advisories provide information on
contaminants that can cause human
health effects and are known or
anticipated to occur in drinking water.
The EPA’s health advisories are nonenforceable and non-regulatory and
provide technical information to state
agencies on health effects, analytical
methodologies, and treatment
technologies associated with drinking
water contamination. State and local
public health officials have the
discretion to use the perchlorate health
advisory as they deem necessary. The
EPA will consider updating the 2008
perchlorate health advisory in the
future.
C. Occurrence Analysis
The EPA received comments
suggesting that the revised UCMR 1 data
did not provide an adequate estimate of
the perchlorate occurrence in drinking
water systems. Some commenters
indicated that the age of the collected
data rendered the occurrence analysis
obsolete and overestimated, because it
no longer captures current lower
contamination conditions that have
been achieved due to mitigation
measures taken in the Colorado River
Basin. Other commenters criticized the
EPA for replacing UCMR 1 data for
systems located in the States of
California and Massachusetts with more
recent state compliance data for
perchlorate.
The EPA recognizes that changes in
perchlorate levels (increasing or
decreasing) may have occurred in water
systems since the UCMR 1 samples were
collected between 2001 to 2005. The
EPA updated the UCMR 1 data set to
improve its accuracy in representing the
current conditions for states that have
enacted perchlorate regulations since
the UCMR 1 monitoring was conducted.
As outlined in the June 26, 2019
proposal, the EPA updated occurrence
data for California and Massachusetts
with current compliance data as
reported by the states. Systems from
these two states that were sampled
during the UCMR 1 and that had
reported perchlorate detections were
updated with more recently measured
values taken from current compliance
monitoring data from Consumer
Confidence Reports and state-level
perchlorate compliance monitoring data
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to match corresponding water systems
and entry points.
The EPA has determined that the
updated UCMR 1 data are the best
available data collected in accordance
with accepted methods on the frequency
and level of perchlorate occurrence in
drinking water on a national scale.
V. Conclusion
With this withdrawal of the 2011
perchlorate regulatory determination
and final determination not to regulate
perchlorate, the EPA announces that
there will be no NPDWR for perchlorate
at this time. The EPA could consider relisting perchlorate on the CCL and could
proceed to regulation in the future if the
occurrence or health risk information
changes. As with other unregulated
contaminants, the EPA will consider
addressing limited instances of elevated
levels of perchlorate by working with
the affected system and state, as
appropriate.
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VI. References
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Brown, R.S., Chen, H., Dosiou, C., &
Sullivan, S. (2017). 2017 Guidelines of
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American Water Works Association (AWWA)
2008. National Cost Implications of a
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California Department of Public Health.
(2007). State Adoption of a Perchlorate
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water/certlic/drinkingwater/documents/
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Carlisle, J.C., Dowling, K.C., Siegel, D.M., &
Alexeeff, G.V. (2009). A blood lead
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Costeira, M.J., Oliveira, P., Santos, N.C., Ares,
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Baar, A.L. (2017). Maternal thyroid
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and Draft BBDR Model Report for
Perchlorate in Drinking Water.
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level goal for perchlorate in drinking
water.
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Ghassabian, A., Bongers-Schokking J.J.,
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Enslin, and K. Heidecorn. 2019. Review
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(2013). Evaluation of perturbations in
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Morreale de Escobar, G., Obrego´n, M.J., &
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Health Implications of Perchlorate
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Noten, A.M., Loomans, E.M., Vrijkotte, T.G.,
van de Ven, P.M., van Trotsenburg, A.S.,
Rotteveel, J., van Eijsden, M., & Finken,
M.J. (2015). Maternal hypothyroxinaemia
in early pregnancy and school
performance in 5-year-old offspring. Eur
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Pop, V.J., Brouwers, E.P., Vader, H.L.,
Vulsma, T., van Baar, A.L., & de Vijlder,
J.J. (2003). Maternal hypothyroxinemia
during early pregnancy and subsequent
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Pop, V.J., Kuijpens, J.L., van Baar, A.L.,
Verkerk, G., van Son, M.M., de Vijlder,
J.J., Vulsma, T., Wiersinga, W.M.,
Drexhage, H.A., Vader, H.L. (1999). Low
maternal free thyroxine concentrations
during early pregnancy are associated
with impaired psychomotor
development in infancy. Clinical
Endocrinology, 50, 149–155.
SAB for the U.S. EPA. (2013). SAB Advice on
Approaches to Derive a Maximum
Contaminant Level Goal for Perchlorate.
EPA–SAB–13–004.
Thompson, W., Russell, G., Baragwanath, G.,
Matthews, J., Vaidya, B., & ThompsonCoon, J. (2018). Maternal thyroid
hormone insufficiency during pregnancy
and risk of neurodevelopmental
disorders in offspring: A systematic
review and meta-analysis. Clinical
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Contaminant Monitoring Regulation for
Public Water Systems; Final Rule.
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50556. (September 17, 1999).
USEPA. (2002). A review of the reference
dose and reference concentration
process. EPA–630–P–02–002F.
USEPA. (2003). Contaminant Candidate List
Regulatory Determination Support
Document for Aldrin and Dieldrin. EPA–
815–R–03–010. https://www.epa.gov/
sites/production/files/2014-09/
documents/support_cc1_aldrin-dieldrin_
ccl_regdet.pdf.
USEPA. (2005a). Integrated Risk Information
System (IRIS) Chemical Assessment
Summary: Perchlorate (ClO4-) and
Perchlorate Salts. USEPA National
Center for Environmental Assessment.
USEPA. (2008a). Drinking water: Preliminary
regulatory determination on perchlorate.
Federal Register Notice. 73 FR, Page
60262. (October 10, 2008).
USEPA. (2008b). Regulatory Determinations
Support Document for Selected
Contaminants from the Second Drinking
Water Contaminant Candidate List
(CCL2). EPA–815–R–03–010. https://
www.epa.gov/sites/production/files/
2014-09/documents/chapter_4_dcpa_
mono-_and_di-acid_degradates.pdf.
USEPA. (2009a). Drinking Water: Perchlorate
Supplemental Request for Comments.
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Federal Register Notice. 74 FR, Page
41883. (August 19, 2009).
USEPA. (2009b). Inhibition of the SodiumIodide Symporter By Perchlorate: An
Evaluation of Lifestage Sensitivity Using
Physiologically Based Pharmacokinetic
(PBPK) Modeling (Final Report) (EPA/
600/R–08/106A). Washington, DC.
USEPA. (2011). Drinking Water: Regulatory
Determination on Perchlorate. Federal
Register Notice. 76 FR, Page 7762.
(February 11, 2011).
USEPA. (2012). Benchmark Dose Technical
Guidance. EPA 100–R–12–001.
USEPA. (2018). Proposed Approaches to
Inform the Derivation of a Maximum
Contaminant Level Goal for Perchlorate
in Drinking Water. EPA 816–R–19–008.
USEPA. (2019a). Technical Support
Document: Deriving a Maximum
Contaminant Level Goal for Perchlorate
in Drinking Water. EPA 816–R–19–007.
USEPA. (2019b). Perchlorate Occurrence and
Monitoring Report. EPA 816–R–19–003.
USEPA. (2019c). Health Risk Reduction and
Cost Analysis of the Proposed
Perchlorate National Primary Drinking
Water Regulation. EPA 816–R–19–004.
USEPA. (2020a). Note to File—Perchlorate
Water Systems Contact Records. Docket
Number #EPA–HQ–OW–2018–0780–
1688. https://www.regulations.gov/
document?D=EPA-HQ-OW-2018-07801688.
USEPA. (2020b). Perchlorate
Recommendations for Public Water
Systems. EPA 815–F–20–001.
USEPA. (2020c). Comment Response
Document for the 2020 Regulatory
Determination for Perchlorate. EPA 815–
R–20–001.
van Mil, N.H., Steegers-Theunissen, R.P.M.,
Bongers-Schokking, J.J., El Marroun, H.,
Ghassabian, A., Hofman, A., Jaddoe,
V.W.V., Verhulst, F.C., de Rijke, Y.B.,
Steegers, E.A.P., & Tiemeier, H. (2012).
Maternal hypothryoxinemia during
pregnancy and growth of the fetal and
infant head. Reproductive Sciences,
19(12), 1315–1322. doi: 10.1177/
1933719112450338.
Wang, P., Gao, J., Zhao, S., Guo, Y., Wang,
Z., & Qi, F. (2016). Maternal thyroxine
levels during pregnancy and outcomes of
cognitive development in children.
Molecular Neurobiology, 53(4), 2241–
2248. doi:10.1007/s12035–015–9189–z.
Zoeller, R.T., & Rovet, J. (2004). Timing of
thyroid hormone action in the
developing brain: clinical observations
and experimental findings. Journal of
neuroendocrinology, 16(10), 809–818.
Zoeller, R.T., Tan, S.W., & Tyl, R.W. (2007).
General background on the
hypothalamic-pituitary-thyroid (HPT)
axis. Critical reviews in toxicology, 37(1–
2), 11–53.
jbell on DSKJLSW7X2PROD with RULES
List of Subjects
40 CFR Part 141
Environmental protection,
Administrative practice and procedure,
Chemicals, Indians—lands,
Intergovernmental relations, Radiation
VerDate Sep<11>2014
15:52 Jul 20, 2020
Jkt 250001
protection, Reporting and recordkeeping
requirements, Water supply.
40 CFR Part 142
Environmental protection,
Administrative practice and procedure,
Chemicals, Indians—lands, Radiation
protection, Reporting and recordkeeping
requirements, Water supply.
Andrew Wheeler,
Administrator.
[FR Doc. 2020–13462 Filed 7–20–20; 8:45 am]
BILLING CODE 6560–50–P
ENVIRONMENTAL PROTECTION
AGENCY
40 CFR Part 300
[EPA–HQ–SFUND–2003–0010; FRL–10011–
67–Region 7]
National Oil and Hazardous
Substances Pollution Contingency
Plan; National Priorities List: Partial
Deletion of the Omaha Lead Superfund
Site
Environmental Protection
Agency (EPA).
ACTION: Final rule; partial deletion.
AGENCY:
The Environmental Protection
Agency (EPA) Region 7 announces the
deletion of 117 residential parcels of the
Omaha Lead Superfund site (Site or
OLS) located in Omaha, Nebraska, from
the National Priorities List (NPL). The
NPL, promulgated pursuant to section
105 of the Comprehensive
Environmental Response,
Compensation, and Liability Act
(CERCLA) of 1980, as amended, is an
appendix of the National Oil and
Hazardous Substances Pollution
Contingency Plan (NCP). The EPA and
the State of Nebraska, through the
Nebraska Department of Environment
and Energy, determined that all
appropriate Response Actions under
CERCLA were completed at the
identified parcels. However, this
deletion does not preclude future
actions under CERCLA. This partial
deletion pertains to 117 residential
parcels. The remaining parcels will
remain on the NPL and are not being
considered for deletion as part of this
action.
DATES: This action is effective July 21,
2020.
ADDRESSES: EPA has established a
docket for this action under Docket ID
no. EPA–HQ–SFUND–2003–0010. All
documents in the docket are listed on
https://www.regulations.gov website.
Although listed in the index, some
information is not publicly available,
SUMMARY:
PO 00000
Frm 00016
Fmt 4700
Sfmt 4700
i.e., Confidential Business Information
or other information whose disclosure is
restricted by statute. Certain other
material, such as copyrighted material,
is not placed on the internet and will be
publicly available only in hard copy
form. Publicly available docket
materials are available either
electronically https://
www.regulations.gov or in hard copy at
the site information repositories.
Locations, contacts, and viewing hours
of the Site information repositories are:
• EPA Region 7, 11201 Renner
Boulevard, Lenexa, Kansas 66219, open
from 8:00 a.m. and 4:00 p.m. Monday
through Friday, excluding Federal
holidays and facility closures due to
COVID–19. We recommend that you
contact the person identified in the FOR
FURTHER INFORMATION CONTACT section
before visiting the Region 7 office.
• W. Dale Clark Library, located at
215 S 15th Street, Omaha, NE 68102,
open 10:00 a.m. to 8:00 p.m. Monday
through Thursday; 10:00 a.m. to 6:00
p.m. Friday and Saturday; and 1 p.m. to
6 p.m. Sunday, excluding closures due
to COVID–19.
The EPA has temporarily suspended
many Regional Records Centers for
public visitors to reduce the risk of
transmitting COVID–19. In addition,
many site information repositories are
closed and information in these
repositories, including the deletion
docket, has not been updated with
hardcopy or electronic media. For
further information and updates on EPA
Docket Center services, please visit us
online https://www.epa.gov/dockets.
The EPA continues to carefully and
continuously monitor information from
the Centers for Disease Control and
Prevention (CDC), local area health
departments, and our Federal partners
so that we can respond rapidly as
conditions change regarding COVID.
FOR FURTHER INFORMATION CONTACT:
Elizabeth Hagenmaier, Remedial Project
Manager, U.S. Environmental Protection
Agency, Region 7, SEMD/LMSE, 11201
Renner Boulevard, Lenexa, KS 66219,
telephone (913) 551–7939, email:
hagenmaier.elizabeth@epa.gov.
SUPPLEMENTARY INFORMATION: The
portion of the site to be deleted from the
NPL are 117 residential parcels of the
Omaha Lead Superfund site, Omaha,
Nebraska. A Notice of Intent for Partial
Deletion for this Site was published in
the Federal Register on May 12, 2020
(85 FR 27979).
The closing date for comments on the
Notice of Intent for Partial Deletion was
June 11, 2020. No public comments
were received, and EPA has determined
it will proceed with the partial deletion.
E:\FR\FM\21JYR1.SGM
21JYR1
Agencies
[Federal Register Volume 85, Number 140 (Tuesday, July 21, 2020)]
[Rules and Regulations]
[Pages 43990-44002]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2020-13462]
=======================================================================
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ENVIRONMENTAL PROTECTION AGENCY
40 CFR Parts 141 and 142
[EPA-HQ-OW-2018-0780, EPA-HQ-OW-2008-0692, EPA-HQ-OW-2009-0297; FRL-
10011-21-OW]
RIN 2040-AF28
Drinking Water: Final Action on Perchlorate
AGENCY: Environmental Protection Agency (EPA).
ACTION: Final action.
-----------------------------------------------------------------------
SUMMARY: The Environmental Protection Agency (EPA) is announcing its
withdrawal of the 2011 determination to regulate perchlorate in
accordance with the Safe Drinking Water Act, (SDWA). On February 11,
2011, the EPA published a Federal Register document in which the Agency
determined that perchlorate met the SDWA's criteria for regulating a
contaminant. On June 26, 2019, the EPA published a proposed national
primary drinking water regulation (NPDWR) for perchlorate and requested
public comments on multiple alternative actions, including the
alternative of withdrawing the 2011 regulatory determination for
perchlorate. The EPA received approximately 1,500 comments on the
proposed rulemaking. The EPA has considered these public comments and
based on the best available information the Agency is withdrawing the
2011 regulatory determination and is making a final determination not
to regulate perchlorate. The EPA has determined that perchlorate does
not occur ``with a frequency and at levels of public health concern''
within the meaning of the SDWA. In addition, in the judgment of the EPA
Administrator, regulation of perchlorate does not present a
``meaningful opportunity for health risk reduction for persons served
by public water systems.'' Accordingly, the EPA is
[[Page 43991]]
withdrawing its 2011 determination and is making a final determination
not to regulate perchlorate, and therefore will not issue a NPDWR for
perchlorate at this time.
DATES: For purposes of judicial review, the regulatory determination in
this document is issued as of July 21, 2020.
FOR FURTHER INFORMATION CONTACT: Samuel Hernandez, Office of Ground
Water and Drinking Water, Standards and Risk Management Division (Mail
Code 4607M), Environmental Protection Agency, 1200 Pennsylvania Avenue
NW, Washington, DC 20460; telephone number: (202) 564-1735; email
address: [email protected].
SUPPLEMENTARY INFORMATION: This document is organized as follows:
I. General Information
A. Does this action apply to me?
B. How can I get copies of this document and other related
information?
II. Background
A. What is perchlorate?
B. What is the purpose of this action?
C. What is the EPA's statutory authority for this action?
D. Statutory Framework and Perchlorate Regulatory History
III. Withdrawal of the 2011 Regulatory Determination and Final
Determination Not To Regulate Perchlorate
A. May perchlorate have an adverse effect on the health of
persons?
B. Is perchlorate known to occur or is there a substantial
likelihood that perchlorate will occur in public water systems with
a frequency and at levels of public health concern?
C. Is there a meaningful opportunity for the reduction of health
risks from perchlorate for persons served by public water systems?
D. What is the EPA's final regulatory determination on
perchlorate?
IV. Summary of Key Public Comments on Perchlorate
A. SDWA Statutory Requirements and the EPA's Authority
B. Health Effects Assessment
C. Occurrence Analysis
V. Conclusion
VI. References
I. General Information
A. Does this action apply to me?
This action will not impose any requirements on anyone. Instead,
this action notifies interested parties of the EPA's withdrawal of the
2011 regulatory determination for perchlorate and the final regulatory
determination not to regulate perchlorate. Section IV of this document
provides a summary of the key comments received on the June 26, 2019
(84 FR 30524) proposed NPDWR for perchlorate (referred to hereinafter
as ``the 2019 proposal'').
B. How can I get copies of this document and other related information?
The EPA has established a docket for this action under Docket ID
No. EPA-HQ-OW-2018-0780. Publicly available docket materials are
available electronically at https://www.regulations.gov/docket?D=EPA-HQ-OW-2018-0780.
II. Background
A. What is perchlorate?
Perchlorate is a negatively charged inorganic ion that is composed
of one chlorine atom bound to four oxygen atoms (ClO4-),
which is highly stable and mobile in the aqueous environment.
Perchlorate comes from both natural and manmade sources. It is formed
naturally via atmospheric processes and can be found within mineral
deposits in certain geographical areas. It is also produced in the
United States by industrial processes, and the most commonly produced
compounds include ammonium perchlorate and potassium perchlorate used
primarily as oxidizers in solid fuels to power rockets, missiles, and
fireworks. Perchlorate can also result from the degradation of
hypochlorite solutions used for water disinfection. The degradation
into perchlorate occurs when hypochlorite solutions are improperly
stored and handled. For the general population, most perchlorate
exposure is through the ingestion of contaminated food or drinking
water. Above certain levels, perchlorate can prevent the thyroid gland
from getting enough iodine, which can affect thyroid hormone
production. The consequences of insufficient thyroid hormone levels
during human growth and development are well known. For pregnant women
with low iodine levels, sufficient changes in thyroid hormone levels
may cause changes in the child's brain development. In a 2005 report
entitled ``Health Implications of Perchlorate Ingestion'', the National
Research Council stated that: ``fetuses and preterm newborns constitute
the most sensitive populations although infants and developing children
are also considered sensitive populations'' (NRC, 2005). The existence
of a quantifiable relationship between thyroid hormone changes and
neurodevelopmental outcomes has strong support from the literature on
the subject; however, not every study identifies an association between
maternal thyroid hormone levels and the neurodevelopmental outcomes,
and the state of the science on this relationship is constantly
evolving.
B. What is the purpose of this action?
The purpose of this action is to publish the EPA's notice to
withdraw the 2011 regulatory determination, one of the alternative
options in the 2019 proposal, and to issue a final determination not to
regulate perchlorate in drinking water. This document presents the
EPA's basis for this withdrawal and final regulatory determination, and
the EPA's response to key issues raised by commenters in response to
the 2019 proposal.
C. What is the EPA's statutory authority for this action?
The SDWA sets forth three criteria that must be met for the EPA to
issue a maximum contaminant level goal (MCLG) and promulgate a national
primary drinking water regulation (NPDWR). Specifically, the
Administrator must determine that (1) ``the contaminant may have an
adverse effect on the health of persons''; (2) ``the contaminant is
known to occur or there is a substantial likelihood that the
contaminant will occur in public water systems with a frequency and at
levels of public health concern''; and (3) ``in the sole judgment of
the Administrator, regulation of such contaminant presents a meaningful
opportunity for health risk reduction for persons served by public
water systems'' (SDWA 1412(b)(1)(A)).
SDWA 1412(b)(1)(B) sets out the process for the EPA to establish
drinking water standards for an unregulated contaminant. As explained
in more detail below, in 2011, the EPA issued a determination that
perchlorate met the three statutory criteria outlined above and
therefore should be regulated. Under the statute, a determination to
regulate triggers a duty for the EPA to issue a proposed drinking water
standard within two years and a final rule 18 months later (with the
possibility of a 3 month extension). SDWA 1412(b)(1)(E). The EPA
subsequently published a proposed drinking water standard for
perchlorate, and alternatives including the withdrawal of the 2011
regulatory determination, in 2019. The promulgation of a final drinking
water standard would, when effective, require monitoring of public
water supplies for the contaminant and treatment as necessary to meet
the regulatory standard.
The EPA has determined, based on reviewing data and analysis
obtained since the issuance of the 2011 regulatory determination, that
perchlorate does not meet the statutorily-prescribed criteria for
regulation. As described in Sections III & VI of the 2019 proposal, the
data
[[Page 43992]]
and analysis in the record indicate that perchlorate does not occur in
public water systems with a frequency and at levels of public health
concern. Specifically, the peer-reviewed health effects analysis
indicates that the estimated concentrations of perchlorate that may
represent levels of public health concern (i.e., the proposed MCLG
levels, 18-90 [micro]g/L) is higher than the concentration considered
in issuance of the 2011 regulatory determination (1-47 [micro]g/L)
(USEPA, 2019a). In addition, based on a re-evaluation of the nationally
representative First Unregulated Contaminant Monitoring Rule (UCMR 1)
data, the updated occurrence analysis shows that the frequency of
occurrence of perchlorate in public water systems at levels exceeding
any of the alternative proposed MCLGs (18 [micro]g/L-90 [micro]g/L) is
significantly lower (0.03%-0.002%) than the frequency considered in the
analysis for the 2011 regulatory determination (4%-0.39%) (USEPA,
2019b). The EPA estimates that, even at the most stringent regulatory
level considered in the 2019 proposal (18 [micro]g/L), not more than 15
systems (0.03% of all water systems in the U.S. serving approximately
620,000 people) would need to take action to reduce levels of
perchlorate. Based on this information, the EPA determines that
perchlorate does not occur in public water systems ``with a frequency
and at levels of public health concern'' and thus does not meet the
second criterion of the three required for regulation under the SDWA.
In addition, while the third criterion is ``in the sole judgment of the
Administrator,'' the small number of water systems with perchlorate
levels greater than identified thresholds, and the correspondingly
small population served, provides ample support for the EPA's
conclusion that the regulation of perchlorate does not present a
``meaningful opportunity for health risk reduction for persons served
by public water systems,'' within the meaning of 1412(b)(1)(A)(iii).
Accordingly, because perchlorate no longer meets the statutory criteria
for regulation, the EPA does not have the authority to issue a MCLG or
promulgate a NPDWR for perchlorate.
While the EPA has not previously withdrawn a regulatory
determination, the decision is supported by the legislative history
underlying the 1996 amendments to the SDWA, which repealed the
statutory requirement for the EPA to regulate an additional 25
contaminants every 3 years and replaced it with the current requirement
for the EPA to determine whether regulation is warranted for five
contaminants every five years. In describing the need for such
amendment, the legislative history points to the view expressed at the
Committee Hearing that ``the current law is a one-size-fits-all
program. It forces our water quality experts to spend scarce resources
searching for dangers that often do not exist rather than identifying
and removing real health risks from our drinking water'' (S. Rep. 104-
169 (1995) at 12). This amendment reflected Congress' clear intent that
the EPA prioritize actual health risks in determining whether to
regulate any particular contaminant. See id at 12 (noting that the
amendment ``repeals the requirement that the EPA regulate an additional
25 contaminants every 3 years replacing it with a new selection process
that gives the EPA the discretion to identify contaminants that warrant
regulation in the future'').
The EPA's decision to withdraw the regulatory determination is also
consistent with Congress' direction to prioritize SDWA decisions based
on the best available public health information. See
1412(b)(1)(B)(ii)(II) (findings supporting a determination to regulate
``shall be based on the best available public health information'');
1412(b)(2)(A) (requiring that the EPA use ``the best available, peer-
reviewed science and supporting studies . . .'' in carrying out any
actions under this section). Although the EPA determined in 2011 that
perchlorate met the criteria for regulation, new data and analysis
developed by the Agency as part of the 2019 proposal demonstrate that
the occurrence and health effects information used as the basis for the
2011 determination no longer constitute ``best available information,''
are no longer accurate, and no longer support the Agency's
prioritization of perchlorate for regulation. Accordingly, not only is
the EPA not authorized to issue a MCLG or promulgate a NPDWR for
perchlorate, but it would not be in the public interest for the EPA to
do so.
The EPA recognizes that the SDWA does not include a provision
explicitly authorizing withdrawal of a regulatory determination.
However, such authority is inherent in the authority to issue a
regulatory determination under 1412(b)(1)(B)(ii)(II), particularly
given the requirement that such determination be based on the ``best
available public health information,'' as discussed above. Accordingly,
the EPA must have the inherent authority to withdraw a regulatory
determination if the underlying information changes between regulatory
determination and promulgation. In light of Congress's concern that the
EPA focus new contaminant regulations on priority health concerns,
Congress could not have intended that the EPA's regulatory decision-
making be hamstrung by older data when newer, more accurate scientific
and public health data are available, especially when those data
demonstrate that regulation of a new contaminant would not present a
meaningful opportunity for health risk reduction.
Moreover, the EPA notes that the statute specifically provides that
a decision not to regulate a contaminant is a final Agency action
subject to judicial review. SDWA 1412(b)(1)(B)(ii)(IV). Congress could
have--but did not--specify the same with respect to determinations to
regulate. Congress also did not explicitly prohibit the EPA from
withdrawing or modifying a regulatory determination. Congress' silence
with respect to determinations to regulate suggests that Congress
intended that such a determination is not itself a final agency action,
but rather a preliminary step in a decision-making process culminating
in a NPDWR and thus subject to reconsideration based on new data and
analysis considered during the 36 month promulgation process specified
in the statute. Accordingly, reconsideration of this preliminary
finding--and withdrawal of the determination based on subsequent
analysis mandated for NPDWR development--is fully consistent with the
statutory decision-making framework.
D. Statutory Framework and Perchlorate Regulatory History
Section 1412(b)(1)(B)(i) of the SDWA requires the EPA to publish
every five years a Contaminant Candidate List (CCL). The CCL is a list
of drinking water contaminants that are known or anticipated to occur
in public water systems and are not currently subject to federal
drinking water regulations. The EPA uses the CCL to identify priority
contaminants for regulatory decision-making and information collection.
The placement of a substance on the CCL does not require that it be
regulated under the SDWA. Contaminants listed on the CCL may require
future regulation under the SDWA. The EPA included perchlorate on the
first, second, and third CCLs published in 1998 (63 FR 10274, March 2,
1998), 2005 (70 FR 9071, February 24, 2005), and 2009 (74 FR 51850,
October 8, 2009).
The EPA collects data on the CCL contaminants to better understand
their potential health effects and to determine
[[Page 43993]]
the levels at which they occur in public water systems. SDWA
1412(b)(1)(B)(ii) requires that, every five years, the EPA, after
consideration of public comment, issue a determination of whether or
not to regulate at least five contaminants on each CCL. For any
contaminant that the EPA determines meets the criteria for regulation
under SDWA 1412(b)(1)(E), the EPA must propose a NPDWR within two years
and promulgate a final regulation within 18 months of the proposal
(which may be extended by 9 additional months).
As part of its responsibilities under the SDWA, the EPA implements
section 1445(a)(2) (``Monitoring Program for Unregulated
Contaminants''). This section requires that once every five years, the
EPA issue a list of no more than 30 unregulated contaminants to be
monitored by public water systems. This monitoring is implemented
through the Unregulated Contaminant Monitoring Rule (UCMR), which
collects data from community water systems and non-transient, non-
community water systems. The first four UCMRs collected data from a
census of large water systems (serving more than 10,000 people) and
from a statistically representative sample of small water systems. On
September 17, 1999, the EPA published its first UCMR (64 FR 50556),
which required all large systems and a representative sample of small
systems to monitor for perchlorate and 25 other contaminants (USEPA,
1999). Water system monitoring data for perchlorate were collected from
2001 to 2005.
The EPA and other federal agencies asked the National Research
Council (NRC) to evaluate the health implications of perchlorate
ingestion. In its 2005 report, the NRC concluded that perchlorate
exposure inhibits the transport of iodide \1\ into the thyroid by a
protein molecule known as the sodium/iodide symporter (NIS), which may
lead to decreases in the production of two thyroid hormones, thyroxine
(T3) and triiodothyronine (T4), and increases in the production of
thyroid-stimulating hormone (TSH) (National Research Council (NRC),
2005). Additionally, the NRC concluded that the most sensitive
population to perchlorate exposure are ``the fetuses of pregnant women
who might have hypothyroidism or iodide deficiency'' (p. 178). The EPA
established a reference dose (RfD) consistent with the NRC's
recommended RfD of 0.7 [micro]g/kg/day for perchlorate. The reference
dose is an estimate of a human's daily exposure to perchlorate that is
likely to be without an appreciable risk of adverse effects. This RfD
was based on a study (Greer, Goodman, Pleus, & Greer, 2002) of
perchlorate's inhibition of radioactive iodine uptake in healthy adults
and the application of an uncertainty factor of 10 for intraspecies
variability (USEPA, 2005a).
---------------------------------------------------------------------------
\1\ For the purposes of this document, ``iodine'' will be used
to refer to dietary intake before entering the body. Once in the
body, ``iodide'' will be used to refer to the ionic form.
---------------------------------------------------------------------------
In October 2008, the EPA published a preliminary regulatory
determination not to regulate perchlorate in drinking water and
requested public comment (73 FR 60262, October 10, 2008). In that
preliminary determination, the EPA found that perchlorate did not occur
with a frequency and at levels of public health concern within the
meaning of the SDWA, and that development of a regulation did not
present a meaningful opportunity for health risk reduction for persons
served by public water systems. In reaching this conclusion, the EPA
derived and used a Health Reference Level (HRL) of 15 [mu]g/L based on
the RfD of 0.7 [micro]g/kg/day and body weight and exposure information
for pregnant women (USEPA, 2008a). Using the UCMR 1 occurrence data,
the EPA estimated that less than 1% of drinking water systems (serving
approximately 1 million people) had perchlorate levels above the HRL of
15 [micro]g/L. Based on this information, the EPA found that
perchlorate did not occur at a frequency and at levels of public health
concern. The EPA also determined there was not a meaningful opportunity
for a NPDWR for perchlorate to reduce health risks.
In August 2009, the EPA published a supplemental request for
comment with new analysis that derived potential alternative Health
Reference Levels (HRLs) for 14 life stages, including infants and
children. The analysis used the RfD of 0.7 [mu]g/kg/day and life stage-
specific bodyweight and exposure information, resulting in comparable
perchlorate concentrations in drinking water, based on life stage, of
between 1 [mu]g/l to 47 [mu]g/l (74 FR 41883; USEPA, 2009a).
In February 11, 2011, the EPA published its determination to
regulate perchlorate (76 FR 7762; USEPA, 2011) after careful
consideration of public comments on the October 2008 and August 2009
notices. The EPA found at that time that perchlorate may have an
adverse effect on the health of persons; that it is known to occur, or
that there is a substantial likelihood that it will occur, in public
drinking water systems with a frequency and at levels that present a
public health concern; and that regulation of perchlorate presented a
meaningful opportunity for health risk reduction for persons served by
public water systems. The EPA found that as many as 16 million people
could potentially be exposed to perchlorate at levels of concern, up
from 1 million people originally estimated in the 2008 notice.
As a result of the determination, and as required by SDWA
1412(b)(1)(E), the EPA initiated the process to develop a MCLG and a
NPDWR for perchlorate.
In September 2012, the U.S. Chamber of Commerce (the Chamber)
submitted to the EPA a Request for Correction under the Information
Quality Act regarding the EPA's regulatory determination.\2\ In the
request, the Chamber claimed that the UCMR 1 data used in the EPA's
occurrence analysis did not comply with data quality guidelines and
were not representative of current conditions. In response to this
request, the EPA reassessed the data and removed certain source water
samples that could be paired with appropriate follow-up samples located
at the entry point to the distribution system. The EPA also updated the
UCMR 1 data in the analysis for systems in California and
Massachusetts, using state compliance data to reflect current
occurrence conditions after state regulatory limits for perchlorate
were implemented. For more information on the Chamber's request and the
EPA's response, see the Perchlorate Occurrence and Monitoring Report
(USEPA, 2019b).
---------------------------------------------------------------------------
\2\ The U.S. Chamber of Commerce letter to the EPA and other
corresponding records are available at https://www.epa.gov/quality/epa-information-quality-guidelines-requests-correction-and-requests-reconsideration#12004.
---------------------------------------------------------------------------
As required by section 1412(d) of the SDWA, as part of the NPDWR
development process, the EPA requested comments from the Science
Advisory Board (SAB) in 2012, seeking guidance on how best to consider
and interpret the life stage information, the epidemiologic and
biomonitoring data since the NRC report, physiologically-based
pharmacokinetic (PBPK) analyses, and the totality of perchlorate health
information to derive an MCLG for perchlorate. In May 2013, the SAB
recommended that the EPA:
Derive a perchlorate MCLG that addresses sensitive life
stages through physiologically-based pharmacokinetic/pharmacodynamic
modeling based upon its mode of action, rather than the default MCLG
approach using the RfD and specific chemical exposure parameters;
expand the modeling approach to account for thyroid
hormone perturbations and potential adverse
[[Page 43994]]
neurodevelopmental outcomes from perchlorate exposure;
utilize a mode-of-action framework for developing the MCLG
that links the steps in the proposed mechanism leading from perchlorate
exposure through iodide uptake inhibition--to thyroid hormone changes--
and finally to neurodevelopmental impacts; and
``[e]xtend the [BBDR] model expeditiously to . . . provide
a key tool for linking early events with subsequent events as reported
in the scientific and clinical literature on iodide deficiency, changes
in thyroid hormone levels, and their relationship to neurodevelopmental
outcomes during sensitive early life stages''(SAB for the U.S. EPA,
2013, p. 19).
To address the SAB recommendations, the EPA revised an existing
PBPK/PD model that describes the dynamics of perchlorate, iodide, and
thyroid hormones in a woman during the third trimester of pregnancy
(Lumen, Mattie, & Fisher, 2013; USEPA, 2009b). The EPA also created its
own Biologically Based Dose Response (BBDR) models that included the
additional sensitive life stages identified by the SAB, i.e., breast-
and bottle-fed neonates and infants (SAB for the U.S. EPA, 2013, p.
19).
To determine whether the Agency had implemented the SAB
recommendations for modeling thyroid hormone changes, the EPA convened
an independent peer review panel to evaluate the BBDR models in January
2017 (External Peer Reviewers for USEPA, 2017). The EPA considered the
recommendations from the 2017 peer review and made necessary model
revisions to increase the scientific rigor of the model and the
modeling results, including extending the BBDR model to the first
trimester and incorporating the TSH feedback mechanism.
The EPA convened a second independent peer review panel in January
2018 to evaluate the revisions to the BBDR model, including the
transition from the third to the first trimester as the life stage of
interest. The EPA also presented several approaches to link the thyroid
hormone changes in a pregnant mother predicted by the BBDR model to
neurodevelopmental effects using evidence from the epidemiological
literature (External Peer Review for U.S. EPA, 2018).
In response to a lawsuit brought to enforce the deadlines in SDWA
1412(b)(1)(E) triggered by the 2011 regulatory determination for
perchlorate, on October 18, 2016, the U.S. District Court for the
Southern District of New York entered a consent decree, requiring the
EPA to sign for publication a proposal for a MCLG and NPDWR for
perchlorate in drinking water no later than October 31, 2018, and to
sign for publication a final MCLG and NPDWR for perchlorate in drinking
water no later than December 19, 2019. The deadline for the EPA to
propose a MCLG and NPDWR for perchlorate in drinking water was later
extended to May 28, 2019, and the date for signature of a final MCLG
and NPDWR was extended to no later than June 19, 2020. The consent
decree is available in the docket for this action.
In compliance with the deadline established in the consent decree,
on May 23, 2019, the EPA Administrator signed a proposed rulemaking
document seeking public comment on a range of options regarding the
regulation of perchlorate in public drinking water systems. The
proposed rulemaking document was published in the Federal Register on
June 26, 2019. 84 FR 30524. The EPA proposed a NPDWR for perchlorate
with an MCL and MCLG of 56 [micro]g/L. The proposed MCLG of 56
[micro]g/L was based on avoiding an estimated 2 point IQ decrement
associated with exposure to perchlorate in drinking water during the
most sensitive life stage (the fetus) within a specific segment of the
population (iodine deficient pregnant women).
The EPA also requested comment on two alternative MCL/MCLG values
of 18 [micro]g/L and 90 [micro]g/L. These alternatives were based upon
avoiding an estimated 1 point and 3 point IQ decrement respectively,
associated with perchlorate exposure. Additionally, the EPA requested
comment on whether the 2011 regulatory determination should be
withdrawn, based on new information including updated occurrence data
on perchlorate in drinking water and new analysis of the concentration
of perchlorate in drinking water that represents a level of health
concern.
III. Withdrawal of the 2011 Regulatory Determination and Final
Determination Not To Regulate Perchlorate
In determining whether to regulate a particular contaminant, the
EPA must follow the criteria mandated by the 1996 SDWA Amendments.
Specifically, in order to issue a MCLG and NPDWR for perchlorate, the
EPA must determine that perchlorate ``may have an adverse effect on the
health of persons,'' that perchlorate occurs at ``a frequency and at
levels of public health concern'' in public water systems, and that
regulation of perchlorate in drinking water systems ``presents a
meaningful opportunity for health risk reduction for persons served by
public water systems.'' SDWA 1412(b)(1)(A). In preparing the 2019
proposal for perchlorate, the EPA updated and improved information on
the levels of public health concern and the frequency and levels of
perchlorate in public water systems. The following is the EPA's
reassessment of the regulatory determination criteria applied to the
best available health science and occurrence data for perchlorate.
A. May perchlorate have an adverse effect on the health of persons?
Yes, perchlorate may have adverse health effects above certain
exposure levels. The perchlorate anion is biologically significant
specifically with respect to the functioning of the thyroid gland.
Above certain exposure levels, perchlorate can interfere with the
normal functioning of the thyroid gland by inhibiting the transport of
iodide into the thyroid, resulting in a deficiency of iodide in the
thyroid. Perchlorate inhibits (or blocks) iodide transport into the
thyroid by chemically competing with iodide, which has a similar shape
and electric charge. The transfer of iodide from the blood into the
thyroid is an essential step in the synthesis of thyroid hormones.
Thyroid hormones play an important role in the regulation of metabolic
processes throughout the body and are also critical to developing
fetuses and infants, especially for brain development. Because the
developing fetus depends on an adequate supply of maternal thyroid
hormones for its central nervous system development during the first
and second trimester of pregnancy, iodide uptake inhibition from
perchlorate exposure has been identified as a concern in connection
with increasing risk of neurodevelopmental impairment in fetuses of
pregnant women with low dietary iodine. Poor iodide uptake and
subsequent impairment of the thyroid function in pregnant and lactating
women have been linked to delayed development and decreased learning
capability in their infants and children (NRC, 2005). There is
scientific evidence to support that perchlorate can reduce iodide
uptake and therefore alter the level of thyroid hormones. There is also
scientific evidence that changes in thyroid hormone levels in a
pregnant woman may be linked to changes in the neurodevelopment of her
offspring. The existence of a quantifiable relationship between thyroid
hormone changes and neurodevelopmental outcomes has strong support from
the literature on the subject; however, not every study identifies an
association between maternal thyroid hormone levels and the
neurodevelopmental outcomes and
[[Page 43995]]
the state of the science on this relationship is constantly evolving.
Therefore, the EPA continues to find that perchlorate may have an
adverse effect on the health of persons above certain exposure levels
based on its ability to interfere with thyroid hormone production.
B. Is perchlorate known to occur or is there a substantial likelihood
that perchlorate will occur in public water systems with a frequency
and at levels of public health concern?
The EPA has determined that perchlorate does not occur with a
frequency and at levels of public health concern in public water
systems. The EPA has made this determination by comparing the best
available data on the occurrence of perchlorate in public water systems
with potential MCLGs for perchlorate.
In past regulatory determinations, the EPA has identified HRLs as
benchmarks against which the EPA compares the concentration of a
contaminant found in public water systems to determine whether it
occurs at levels of public health concern. For the 2011 regulatory
determination, the EPA identified potential alternative HRL values
ranging from 1 to 47 [micro]g/L for 14 different life stages. These
HRLs were not final decisions about the level of perchlorate in
drinking water that is without adverse effects. For the 2019 proposal,
the EPA derived three potential MCLGs for perchlorate of 18, 56, and 90
[mu]g/L for the most sensitive life stage using the best available peer
reviewed science in accordance with the SDWA. After considering public
comment, the EPA used these potential MCLGs as the levels of public
health concern in assessing the frequency of occurrence of perchlorate
in this regulatory determination. These MCLGs were set at levels to
avoid estimated IQ decrements of 1, 2, and 3 points respectively in the
most sensitive life stage, the children of hypothyroxinemic women with
low iodine intake. The EPA proposed an MCLG of 56 [mu]g/L and
alternative MCLG values of 18 and 90 [mu]g/L.
The rationale used in deriving the numerical values is presented in
greater detail in the EPA technical support document entitled
``Deriving a Maximum Contaminant Level Goal for Perchlorate in Drinking
Water'' (USEPA, 2019a).
The EPA compared these potential MCLG values with the updated
perchlorate UCMR 1 occurrence data set. A comprehensive description of
the perchlorate occurrence data is presented in Section VI of the 2019
proposal. It is also available in the ``Perchlorate Occurrence and
Monitoring Report'' (USEPA, 2019a).
The occurrence data for perchlorate were collected from 3,865 PWSs
between 2001 and 2005 under the UCMR 1. In the 2019 proposal, the EPA
modified the UCMR 1 data set in response to concerns raised by
stakeholders regarding the data quality and to represent current
conditions in California and Massachusetts, which have enacted
perchlorate regulations since the UCMR 1 data were collected.
Massachusetts promulgated a drinking water standard for perchlorate of
2 [mu]g/L in 2006 (MassDEP, 2006), and California promulgated a
drinking water standard of 6 [mu]g/L in 2007 (California Department of
Public Health, 2007). Systems in these states are now required to keep
perchlorate levels in drinking water below their state limits. As
discussed below, the EPA finds that perchlorate levels in drinking
water and sources of drinking water have decreased since the UCMR 1
data collection. The main factors contributing to the decrease in
perchlorate levels are the promulgation of drinking water regulations
for perchlorate in California and Massachusetts and the ongoing
remediation efforts in the state of Nevada to address perchlorate
contamination in groundwater adjacent to the lower Colorado River
upstream of Lake Mead.
To update the occurrence data for systems sampled during UCMR 1
from California and Massachusetts, the EPA identified all systems and
corresponding entry points which had reported perchlorate detections in
UCMR 1. Once the systems and entry points with detections were
appropriately identified, the EPA then used publicly available
California and Massachusetts monitoring data for perchlorate, to
replace the original UCMR1 data with more recent data where available
(Perchlorate Occurrence and Monitoring Report, USEPA, 2019b).
The EPA has determined that the UCMR 1 data with these updates are
the best available data collected in accordance with accepted methods
regarding the frequency and level of perchlorate nationally. The UCMR 1
data are from a census of the large water systems (serving more than
10,000 people) and a statistically representative sample of small water
systems that provides the best available, national assessment of
perchlorate occurrence in drinking water.
The EPA used entry point maximum measurements to estimate potential
baseline occurrence and exposure at levels that exceed the potential
MCLG thresholds. The maximum measurements indicate highest perchlorate
levels reported in at least one quarterly sample from surface water
systems and at least one semi-annual sample from ground water systems.
Table 1--Perchlorate Occurrence and Exposure (Updated UCMR 1 Data Set)
----------------------------------------------------------------------------------------------------------------
Percent of U.S.
Entry points with Water systems water systems
Threshold concentration ([micro]g/L) detections above with detections with detections Population served
threshold above threshold above threshold
(percent)
----------------------------------------------------------------------------------------------------------------
18 [micro]g/L....................... 17 15 0.03 620,560
56 [micro]g/L....................... 2 2 0.004 32,432
90 [micro]g/L....................... 1 1 0.002 25,972
----------------------------------------------------------------------------------------------------------------
Table 1 presents the number and percentage of water systems that
reported perchlorate at levels exceeding the three proposed MCLG
threshold concentrations. In summary, the updated perchlorate
occurrence information suggests that at an MCLG of 18 [micro]g/L, there
would be 15 systems (0.03% of all water systems in the U.S.) that would
exceed the threshold, at an MCLG of 56 [micro]g/L, two systems (0.004%
of all water systems in the U.S.) would exceed the threshold, and
finally one system would exceed the MCLG threshold of 90 [micro]g/L.
Based on the analysis of drinking water occurrence presented in the
2019 proposal and the data summarized in Table 1 and the range of
potential MCLGs, the EPA concludes that perchlorate does not occur with
a frequency and at levels of
[[Page 43996]]
public health concern in public water systems.
The EPA notes that in 2008, the EPA stated in its preliminary
regulatory determination that perchlorate did not occur with a
frequency and at levels of public health concern in public water
systems based upon the health effects and occurrence information
available at that time, which indicated that 0.8% of public water
system had perchlorate at levels exceeding the HRL of 15 mg/L. The EPA
also stated that there was not a meaningful opportunity for a NPDWR to
reduce health risks based upon the estimates at that time that 0.9
million people had perchlorate levels above the HRL. The EPA further
notes that the Agency has previously determined CCL1 and CCL2
contaminants did not occur with frequency at levels of public health
concern when the percentage of water systems exceeding the HRL were
greater than the frequency of perchlorate occurrence level at the
proposed MCL (0.004% of all water systems in the U.S.). For example, in
2003 the EPA determined that aldrin did not occur with a frequency and
at levels of public health concern based upon data that showed 0.2% of
water systems had aldrin at levels greater than the HRL. The EPA also
concluded that there was not a meaningful opportunity for health risk
reduction for persons served through a drinking water regulation based
on this occurrence data and the estimate that these systems above the
HRL served approximately 1 million people (USEPA, 2003). In 2008 the
EPA determined that DCPA Mono- and Di-Acid degradates did not occur
with a frequency and at levels of public health concern based on data
that showed 0.03% of water systems exceeded the HRL. The EPA also
concluded that there was not a meaningful opportunity for health risk
reduction through a drinking water regulation based on this occurrence
data and the estimate that these systems above the HRL served
approximately 100,000 people (USEPA, 2008b).
While the EPA has made its conclusion that perchlorate does not
occur at a frequency and at levels of public health concern in public
water systems based on the updated UCMR 1 data in Table 1 above, the
EPA also sought to find additional information about the perchlorate
levels at the 15 water systems that had at least one reported result
greater than 18 [micro]g/L in the updated UCMR 1 data. The EPA found
that perchlorate levels have been reduced at many of these water
systems. Although these water systems were not required to take actions
to reduce perchlorate in drinking water, many had conducted additional
monitoring for perchlorate and found decreased levels or had taken
mitigation efforts to address perchlorate, confirming the EPA's
conclusion described above. The status of each of these systems is
described in Table 2 below and confirms the Agency's conclusion that is
based upon the information in Table 1.
Table 2--Update on Systems With Perchlorate Levels Above 18 [micro]g/L in the UCMR 1
----------------------------------------------------------------------------------------------------------------
Range of UCMR 1
State System name results ([micro]g/L) Update on mitigation and
** levels of perchlorate \++\
----------------------------------------------------------------------------------------------------------------
Florida............................ Sebring Water......... ND-70................. The EPA contacted the
Sebring system in January
2020. Operations personnel
indicated that no follow-
up/updated monitoring data
for perchlorate are
available.
Florida............................ Manatee County ND-30................. Researchers contacted the
Utilities Dept. system to identify the
source of perchlorate.
System personnel
attributed the sole
perchlorate detection
under UCMR 1 to analytical
error. System personnel
indicated that three other
quarterly samples
collected under UCMR 1 as
well as other subsequent
perchlorate sampling
efforts were non-detect.
Source: AWWA (2008).
Georgia............................ Oconee Co.-- 38 (single sample).... Researchers contacted the
Watkinsville. system and found that a
perchlorate contaminated
well was removed from
service in 2003. The
system indicates that
perchlorate is no longer
detected. Source: Luis et
al. (2019).
Louisiana.......................... St. Charles Water ND-24................. The EPA was not able to
District 1 East Bank. identify updated data on
perchlorate levels for
this system.
Maryland........................... City of Aberdeen...... ND-19................. The system's 2018 Consumer
Confidence Report (CCR)
indicates that perchlorate
was not detected.
According to the Maryland
Department of Environment,
perchlorate was not
detected in this system in
2019. In addition,
researchers contacted the
system and found that
there has been no
detection of perchlorate
since treatment was
installed in 2009. Source:
Luis et al. (2019).
Maryland........................... Chapel Hill--Aberdeen ND-20................. The EPA contacted the
Proving Grounds. Chapel Hill System in
January 2020. Water system
personnel indicate that
the Chapel Hill WTP was
taken off-line and was
replaced with a new
treatment plant and five
new production wells. The
new treatment plant
started operations on
January 27, 2020. System
personnel also indicate
that monitoring was
conducted in November 2019
and perchlorate was not
detected in either the
source well water or the
finished water. In
addition, according to the
Maryland Department of
Environment, perchlorate
was not detected in this
system in 2019.
[[Page 43997]]
Mississippi........................ Hilldale Water ND-20................. The EPA contacted the
District. Hilldale System in January
2020. Water system
personnel indicated that
no follow-up/updated
monitoring data for
perchlorate are available.
New Mexico......................... Deming Municipal Water 15-20................. Data from the EPA's SDWIS/
System. FED database indicates
that the entry point that
reported detections in
UCMR 1 (Well #3) is now
inactive (i.e., the
contaminated source is no
longer in use).
Nevada............................. City of Henderson..... 6-23.................. Researchers report that the
perchlorate levels
described in the system's
CCR ranged from non-detect
to 9.7 [micro]g/L. Source:
AWWA (2008).
Ohio............................... Fairfield City PWS.... 6-27.................. The EPA contacted the
Fairfield City System in
January 2020. Water system
personnel indicated that
follow-up monitoring was
conducted after UCMR 1,
between 2002 and 2004. The
Ohio EPA provided copies
of the follow-up
monitoring results which
indicate that results at
the entry point ranged
from non-detect to 13
[micro]g/L.
Ohio............................... Hecla Water ND-32................. The EPA contacted the Hecla
Association--Plant Water Association System
PWS. in January 2020. Water
system personnel indicated
that that no follow-up/
updated monitoring data
for perchlorate are
available.
Oklahoma........................... Enid.................. ND-30................. The EPA reviewed Oklahoma's
monitoring data and did
not find any monitoring
results reported for
perchlorate.
Pennsylvania....................... Meadville Area Water ND-33................. The EPA contacted the
Authority. Meadville System in
January 2020. Water system
personnel indicated that
no follow-up/updated
monitoring data for
perchlorate are available.
Puerto Rico........................ Utuado Urbano......... ND-420................ The EPA contacted the
Puerto Rico Aqueduct and
Sewer Authority (PRASA) in
January 2019. PRASA
personnel indicated that
no updated monitoring data
for perchlorate are
available. NOTE: The PRASA
personnel stated that the
Utuado water system was
significantly impacted by
Hurricane Maria and that
monitoring records from
years prior to 2017 were
lost.
Texas.............................. City of Levelland..... ND-32................. Researchers found that a
water storage tank was the
source of perchlorate
contamination. The wells
feeding the tank were
tested by the state and
perchlorate was not
detected. The water tank
was shut off from service.
Source: Luis et al.
(2019).
----------------------------------------------------------------------------------------------------------------
**Values have been rounded. ND describes a sampling event where perchlorate was not detected at or above the
UCMR 1 minimum reporting level of 4 [micro]g/L. UCMR 1 results collected between 2001 and 2005.
++To obtain updated data and/or information regarding perchlorate levels, the EPA reviewed Consumer Confidence
Reports and other publicly available data, as well as published studies. In addition, the EPA contacted some
water systems for information about current perchlorate levels. (USEPA, 2020a)
C. Is there a meaningful opportunity for the reduction of health risks
from perchlorate for persons served by public water systems?
The EPA's analysis presented in the 2019 proposal demonstrates that
a NPDWR for perchlorate does not present a meaningful opportunity for
health risk reduction for persons served by public water systems. As
discussed above, the EPA found that perchlorate occurs with very low
frequency at levels of public health concern. Based on updated UCMR 1
occurrence information, there were 15 water systems (0.03% of all water
systems in the U.S.) that detected perchlorate in drinking water above
the lowest proposed alternative MCLG of 18 [micro]g/L, and only 1
system had a detection above the proposed alternative MCLG of 90
[micro]g/L. Specifically, Table 1 presents the population served by
PWSs that were monitored under UCMR 1 for which the highest reported
perchlorate concentration was greater than the identified thresholds.
The EPA estimates \3\ that the number of people who may be potentially
consuming water containing perchlorate at levels that could exceed the
levels of concern for perchlorate could range between 26,000 and
620,000.
---------------------------------------------------------------------------
\3\ The values shown in Table 1 are based on the revised UCMR 1
data. The EPA also applied statistical sampling weights to the small
systems results to extrapolate to national results. There was one
small system included in the statistical sample stratum which had a
perchlorate measurement exceeding 18 [micro]g/L. Accordingly, the
EPA estimates that approximately 41,000 small system customers may
be exposed to perchlorate greater than 18 [micro]g/L.
---------------------------------------------------------------------------
The small number of water systems with perchlorate levels greater
than identified thresholds, and the correspondingly small population
served, provides ample support for the EPA's conclusion that the
regulation of perchlorate does not present a ``meaningful opportunity
for health risk reduction for persons served by public water systems,''
within the meaning of SDWA 1412(b)(1)(A)(iii).
While the EPA does not believe that a national primary drinking
water regulation presents a meaningful opportunity for health risk
reduction, the Agency remains committed to
[[Page 43998]]
working with States and communities in addressing perchlorate
contamination of drinking water. For example, the EPA has issued a
document entitled ``Perchlorate Recommendations for Public Water
Systems'' which provides recommendations for actions that systems may
take if there are concerns about perchlorate (USEPA, 2020b). The
document outlines steps public systems can take to address perchlorate
in drinking water, including testing, installing treatment equipment,
and communication with customers.
Although a cost benefit analysis is not one of the three SDWA
criteria for making a regulatory determination, the EPA also considered
the findings of the Health Risk Reduction and Cost Analysis (HRRCA,
USEPA 2019c) as additional information confirming the appropriateness
of the withdrawal of the regulatory determination. The HRRCA for
perchlorate (which was presented in the 2019 proposal) provides a
unique set of economic data indicators that are not available for
regulatory determinations because the HRRCA is required for a proposed
NPDWR under SDWA 1412(b)(3)(C), but is not required to support a
regulatory determination. Accordingly, because the EPA initially
determined that perchlorate met the criteria for regulation and began
the regulatory analysis process, the HRRCA was available with respect
to perchlorate at this stage in the SDWA process, and the Agency
considered this comprehensive economic analysis in informing its
decision to withdraw the regulatory determination.
Specifically, the HRRCA provides a description of the potential
benefits and costs of a drinking water regulation for perchlorate. For
all potential regulatory levels considered for perchlorate (18, 56, and
90 [micro]g/L), the total costs associated with establishing a
regulation (ranging from $9.5 to $18.0 million across discount rates
and levels) were substantially higher than the potential range of
benefits (ranging from $0.3 to $3.7 million) (USEPA, 2019c). The
infrequent occurrence of perchlorate at levels of health concern
imposes high monitoring and administrative cost burdens on public water
systems and the states, while having little impact on health risk
reductions and the associated low estimates of benefits. The EPA is not
finalizing the HRRCA for this final action nor is the EPA conducting an
analysis in accordance with the Regulatory Flexibility Act because the
Agency is not promulgating a final regulation.
Based on a comparison of costs and benefits estimated at the three
potential regulatory levels, the EPA determined in the 2019 proposal
that the benefits of establishing a drinking water regulation for
perchlorate do not justify the potential costs.
A drinking water regulation for perchlorate would impose
significant burdens on states and water systems, mainly associated with
requirements for monitoring, including initial monitoring and long-term
monitoring for over 60,000 systems (see Section VIII of the 2019
proposal for more information), but would result in very few systems
having to take action to reduce perchlorate levels. It is of paramount
importance that water systems (particularly medium, small, and
economically distressed systems) focus their limited resources on
actions that ensure compliance with existing NPDWRs and maintain their
technical, managerial, and financial capacity to improve system
operations and the quality of water being provided to their customers,
rather than spending resources monitoring for contaminants that are
unlikely to occur.
D. What is the EPA's final regulatory determination on perchlorate?
Based on the EPA's analysis of the best available public health
information, and after careful review and consideration of public
comments on the June 2019 proposal, the Agency is withdrawing its 2011
determination and is making a final determination not to regulate
perchlorate. Accordingly, the EPA will not issue a NPDWR for
perchlorate at this time. While the EPA has found that perchlorate may
have an adverse effect on human health above certain exposure levels,
based on the analysis presented in this document and supporting record,
the EPA has determined that perchlorate does not occur in public water
systems with a frequency and at levels of public health concern and
that regulation of perchlorate does not present a meaningful
opportunity to reduce health risks for persons served by public water
systems. This conclusion is based on the best available peer reviewed
science and data collected in accordance with accepted methods on
perchlorate health effects and occurrence.
IV. Summary of Key Public Comments on Perchlorate
The EPA received approximately 1,500 comments from individuals or
organizations on the June 2019 proposal. This section briefly discusses
the key technical issues raised by commenters and the EPA's response.
Comments are also addressed in the ``Comment Response Document for the
Final Regulatory Action for Perchlorate'' (USEPA, 2020c) available at
https://www.regulations.gov (Docket ID No. EPA-HQ-OW-2018-0780).
A. SDWA Statutory Requirements and the EPA's Authority
The EPA received comments stating that the Agency should promulgate
an MCLG and MCL for perchlorate and comments stating that the Agency
should not promulgate a regulation. After considering these comments,
the EPA has re-evaluated perchlorate in accordance with SDWA
1412(b)(1)(A), which requires that the Agency promulgate a NPDWR if (i)
the contaminant may have an adverse effect on the health of persons;
(ii) the contaminant is known to occur or there is a substantial
likelihood that the contaminant will occur in public water systems with
a frequency and at levels of public health concern; and (iii) in the
sole judgment of the Administrator, regulation of such contaminant
presents a meaningful opportunity for health risk reduction for persons
served by public water systems.
The EPA has determined, based upon the best available peer reviewed
science and data collected in accordance with accepted methods, that
perchlorate does not occur at a frequency and at levels of public
health concern, and that regulation of perchlorate does not present a
meaningful opportunity for health risk reduction. Because perchlorate
does not meet the statutory criteria for regulation, the EPA lacks the
authority to issue a MCLG or NPDWR for perchlorate, and, is therefore
withdrawing its 2011 regulatory determination and issuing this final
determination not to regulate perchlorate. For more information
regarding the EPA's statutory authority to withdraw its regulatory
determination, see Section II.C above.
B. Health Effects Assessment
Health Effects/MCLG Derivation
The EPA received comments indicating that the Agency should utilize
different approaches to derive the MCLG for perchlorate including
approaches that some states used to develop their perchlorate advisory
levels or drinking water standards. The EPA considered a number of
alternative approaches to develop the MCLG for perchlorate and in
accordance with SDWA 1412(e), the Agency sought recommendations from
the Science Advisory Board. The EPA derived the proposed MCLG for
perchlorate based on the approach recommended by the Science Advisory
Board (SAB) (SAB for
[[Page 43999]]
the U.S. EPA, 2013). The SAB recommended that ``the EPA derive a
perchlorate MCLG that addresses sensitive life stages through
physiologically-based pharmacokinetic/pharmacodynamic modeling based
upon its mode of action rather than the default MCLG approach using the
RfD and specific chemical exposure parameters.'' The EPA has
implemented these recommendations and has obtained two independent peer
reviews of the analysis. These peer reviewers stated that: ``[o]verall,
the panel agreed that the EPA and its collaborators have prepared a
highly innovative state-of-the-science set of quantitative tools to
evaluate neurodevelopmental effects that could arise from drinking
water exposure to perchlorate. While there is always room for
improvement of the models, with limited additional work to address the
committee's comments below, the current models are fit-for-purpose to
determine an MCLG'' (External Peer Reviewers for USEPA, 2018, p. 2).
The EPA received comments indicating that the most sensitive life
stages were not selected and/or considered in the Agency's approach.
The EPA disagrees. Gestational exposure to perchlorate during
neurodevelopment is the most sensitive time period. The NRC concluded
that the population most sensitive to perchlorate exposure are ``the
fetuses of pregnant women who might have hypothyroidism or iodide
deficiency'' (p. 178, NRC 2005). In addition, there is clear evidence
that disrupted maternal thyroid hormone levels during gestation can
impact neurodevelopment later in life (Alexander et al., 2017; Costeira
et al., 2011; Endendijk et al., 2017; Ghassabian, Bongers-Schokking,
Henrichs, Jaddoe, & Visser, 2011; Glinoer & Delange, 2000; Glinoer &
Rovet, 2009; Gyllenberg et al., 2016; Henrichs et al., 2010; Korevaar
et al., 2016; Morreale de Escobar, Obreg[oacute]n, & Escobar del Rey,
2004; Noten et al., 2015; Pop et al., 2003, 1999; SAB for the U.S. EPA,
2013; Thompson et al., 2018; van Mil et al., 2012; Wang et al., 2016;
Zoeller & Rovet, 2004; Zoeller et al., 2007). The available data
demonstrate that the fetus of the first trimester pregnant mother, when
compared to other life-stages, experiences the greatest impact from the
same dose of perchlorate, which is described in detail in Section 6 of
the document ``Deriving a Maximum Contaminant Level Goal for
Perchlorate in Drinking Water'' (USEPA, 2019a). Some commenters
suggested that the bottle-fed infant is a more sensitive life-stage.
The EPA disagrees. As described in the January 2017 Peer Review Report
on the original Biologically Based Dose Response (BBDR) model, the
bottle-fed infant's thyroid hormone levels were not impacted by doses
of perchlorate up to 20 [micro]g/day (External Peer Reviewers for
USEPA, 2017). This lack of any impact is due primarily to the iodine in
the formula, which offsets the impact of perchlorate on the thyroid.
The EPA received comments advocating for the use of the population-
based approach evaluating the shift in the proportion of a population
that would fall below a hypothyroxinemic cut point under a perchlorate
exposure scenario. The EPA chose to develop the MCLG using dose-
response functions from the epidemiological literature to estimate
neurodevelopmental impacts in the offspring of pregnant women exposed
to perchlorate. The EPA selected this proposed approach because it is
consistent with the SDWA's definition of a MCLG to avoid adverse health
effects and because it is most consistent with the SAB recommendations.
In addition, given that thyroid hormone levels vary by reference
population and that there is not a defined threshold for the
concentration of fT4 representing hypothyroxinemia makes the
population-based approach less desirable than the approach selected
(USEPA, 2018).
End Point Selection/Basis
The EPA received comments regarding the magnitude of an IQ change
which should be used in deriving the MCLG. The EPA's proposed MCLG was
based upon avoiding a 2% change in IQ in the most sensitive life stage,
and the EPA also requested comment on alternative options for the MCLG
that would respectively avoid 1% or 3% change in IQ in the most
sensitive life stage. Many comments stated that the EPA should at most
consider a 1% IQ change. However, several commenters stated that a 3%
change is too small to have a meaningful impact and suggested that the
EPA consider a higher IQ percent change.
The EPA uses a variety of science policy approaches to select
points of departure for developing regulatory values. For instance, in
noncancer risk assessment, the EPA often uses a percentage change in
value. When assessing toxicological data, a 10% extra risk (for
discrete data), or a 1 standard deviation (i.e., 15 IQ points) change
from the mean (for continuous data) is often used (USEPA, 2012). A
smaller response to inform a POD has been applied when using
epidemiological literature, because there is an inherently more direct
relationship between the study results and the exposure context and
health endpoint.
Given the difficulty in identifying a response below which no
adverse impact occurs when considering a continuous outcome in the
human population, the EPA looked to its Benchmark Dose Guidance (2012)
for insight regarding a starting point. Specifically, ``[a] BMR of 1%
has typically been used for quantal human data from epidemiology
studies'' (p. 21, USEPA, 2012). For the specific context of setting an
MCLG for perchlorate, the EPA evaluated the level of perchlorate in
water associated with a 1% decrease, a 2% decrease, and a 3 percent
decrease in the mean population IQ (i.e., 1, 2 and 3 IQ points).
In evaluating the frequency and level of occurrence of perchlorate
in drinking water, the EPA has found that perchlorate does not occur
with frequency even at the lowest alternative MCLG of 18 [micro]g/L,
which is based upon avoiding a 1% change in IQ in the most sensitive
life stage.
The EPA received comments that the proposed MCLG did not
incorporate an adequate margin of safety to comply with the SDWA. The
EPA disagrees that it failed to use an adequate margin of safety. The
EPA's assessment focused upon the most sensitive subset of the
population, specifically offspring whose mothers had low (75 [micro]g/
day) iodine intake and were hypothyroxinemic (fT4 in the lowest 10th
percentile of the population). In addition, to account for
uncertainties and to ensure that the most sensitive subset of the
population is protected with an adequate margin of safety, a 3-fold
uncertainty factor was applied to the proposed MCLG calculation (USEPA,
2019a). More discussion on the uncertainty factor is presented below,
in the section entitled ``Consideration of Uncertainties.''
The EPA received some comments stating that the selection of the
study for informing the relationship between maternal hormone levels
(fT4) and IQ was inadequately described. Other comments supported the
EPA's study selection. The EPA concludes that selection of the Korevaar
et al. (2016) study is appropriate because that study provides the most
robust data available with a clear measure of neurodevelopment that can
be expressed as a function of changing maternal fT4 exposure, which is
necessary to the development of the model.
[[Page 44000]]
BBDR and PBPK Models
The EPA received comments indicating that the BBDR model was not
transparent, scientifically valid, or based on robust data. The EPA
disagrees. The model represents the best available peer reviewed
science and uses the best available data to inform a MCLG for
perchlorate. The EPA disagrees with the suggestion that there is a
significant lack of transparency with respect to the assumptions
related to the BBDR model. Appendix A of the EPA's Proposed MCLG
Approaches report outlines the justification for all assumptions used
in the development of the BBDR model (USEPA, 2019a). The EPA also
disagrees with the assertion that the BBDR model is far too uncertain
to be relied upon as the basis for the derivation of the RfD. The EPA
has used the best available science to calibrate the pharmacokinetic
aspects of the BBDR model. The development of the BBDR model was in
response to SAB recommendations, and a model was deemed to be a more
refined approach to estimating a dose-response relationship between
perchlorate exposure and maternal fT4 than anything that was available
in the current scientific literature. The EPA disputes the claim that
the BBDR model is not scientifically valid, as the Agency conducted a
peer review of the approach proposed and the reviewers concluded that
the approach was ``fit for purpose'' to inform a MCLG for perchlorate
(External Peer Reviewers for U.S. EPA, 2018, p. 2).
Consideration of Uncertainties
The EPA received comments on the Agency's use of Uncertainty
factors (UFs); with most commenters suggesting that the EPA should
consider a higher UF for inter-individual variability. The EPA
thoroughly considered the application of UFs when deriving the RfDs and
followed guidance presented in ``A review of the reference dose and
reference concentration processes'' (USEPA, 2002). The EPA concluded
that the UFs are adequately justified, and subsequently no changes have
been made. Justification for each of the UFs can be found in Section 11
of the Agency's MCLG Derivation report (USEPA, 2019a).
The EPA selected a UF of 3 for inter-individual variability,
because the Agency specifically modeled groups within the population
that are identified as likely to be at greater risk of the adverse
effects from perchlorate in drinking water (i.e., the fetus of the
iodide deficient pregnant mother). The EPA selected model parameters to
account for the most sensitive individuals in that group (i.e., muted
TSH feedback, low fT4 values, low-iodine intake). As discussed in the
MCLG Derivation report, the EPA has attempted to select the most
appropriate inputs to protect the most sensitive population with an
adequate margin of safety (USEPA, 2019a). The EPA has determined that
the selection of a UF of 3 for inter-individual variability is
justified. As described in the MCLG Derivation report, because the
output from the BBDR model is specific to the sensitive population, the
EPA concluded that the UF of 3 is appropriate. In regard to variation
in sensitivity among the members of the human population (i.e., inter-
individual variability), section 4.4.5.3 of the EPA guidance ``A review
of the reference dose and reference concentration process'' (USEPA,
2002) document states, ``In general, the Technical Panel reaffirms the
importance of this UF, recommending that reduction of the intraspecies
UF from a default of 10 be considered only if data are sufficiently
representative of the exposure/dose-response data for the most
susceptible subpopulation(s). Similar to the interspecies UF, the
intraspecies UF can be considered to consist of both a toxicokinetic
and toxicodynamic portion (i.e. 10[caret]0.5 each)'' (USEPA, 2002).
Given that the BBDR model significantly accounts for differences within
the human population, the full UF of 10 is not warranted.
One commenter suggested using a UF greater than 1 to account for
the extrapolation of the lowest-observed adverse effect level (LOAEL)
to the no-observed-adverse-effect-level (NOAEL). LOAELs and NOAELs were
not identified or used by the EPA in its assessment because the Agency
employed a sophisticated BBDR modeling approach, which was coupled with
extrapolation to changes in IQ using linear regression, to determine a
POD that would not be expected to represent an adverse effect.
Therefore, a UF of 1 is appropriate. Other commenters suggested
incorporating UFs for database deficiencies. Based on the findings of
the NRC report, the EPA has previously concluded that this UF was not
needed for deficiencies in the perchlorate database (NRC, 2005; USEPA,
2005a). The EPA determined that a UF of 1 to account for database
deficiencies is still appropriate, given that the comprehensiveness of
the perchlorate database has only increased since 2005.
Health Advisory
Several commenters suggest that the EPA should withdraw the 2011
determination to regulate perchlorate and instead issue an updated
health advisory for perchlorate. The EPA issued an interim health
advisory level for perchlorate in 2008. Health advisories provide
information on contaminants that can cause human health effects and are
known or anticipated to occur in drinking water. The EPA's health
advisories are non-enforceable and non-regulatory and provide technical
information to state agencies on health effects, analytical
methodologies, and treatment technologies associated with drinking
water contamination. State and local public health officials have the
discretion to use the perchlorate health advisory as they deem
necessary. The EPA will consider updating the 2008 perchlorate health
advisory in the future.
C. Occurrence Analysis
The EPA received comments suggesting that the revised UCMR 1 data
did not provide an adequate estimate of the perchlorate occurrence in
drinking water systems. Some commenters indicated that the age of the
collected data rendered the occurrence analysis obsolete and
overestimated, because it no longer captures current lower
contamination conditions that have been achieved due to mitigation
measures taken in the Colorado River Basin. Other commenters criticized
the EPA for replacing UCMR 1 data for systems located in the States of
California and Massachusetts with more recent state compliance data for
perchlorate.
The EPA recognizes that changes in perchlorate levels (increasing
or decreasing) may have occurred in water systems since the UCMR 1
samples were collected between 2001 to 2005. The EPA updated the UCMR 1
data set to improve its accuracy in representing the current conditions
for states that have enacted perchlorate regulations since the UCMR 1
monitoring was conducted. As outlined in the June 26, 2019 proposal,
the EPA updated occurrence data for California and Massachusetts with
current compliance data as reported by the states. Systems from these
two states that were sampled during the UCMR 1 and that had reported
perchlorate detections were updated with more recently measured values
taken from current compliance monitoring data from Consumer Confidence
Reports and state-level perchlorate compliance monitoring data
[[Page 44001]]
to match corresponding water systems and entry points.
The EPA has determined that the updated UCMR 1 data are the best
available data collected in accordance with accepted methods on the
frequency and level of perchlorate occurrence in drinking water on a
national scale.
V. Conclusion
With this withdrawal of the 2011 perchlorate regulatory
determination and final determination not to regulate perchlorate, the
EPA announces that there will be no NPDWR for perchlorate at this time.
The EPA could consider re-listing perchlorate on the CCL and could
proceed to regulation in the future if the occurrence or health risk
information changes. As with other unregulated contaminants, the EPA
will consider addressing limited instances of elevated levels of
perchlorate by working with the affected system and state, as
appropriate.
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List of Subjects
40 CFR Part 141
Environmental protection, Administrative practice and procedure,
Chemicals, Indians--lands, Intergovernmental relations, Radiation
protection, Reporting and recordkeeping requirements, Water supply.
40 CFR Part 142
Environmental protection, Administrative practice and procedure,
Chemicals, Indians--lands, Radiation protection, Reporting and
recordkeeping requirements, Water supply.
Andrew Wheeler,
Administrator.
[FR Doc. 2020-13462 Filed 7-20-20; 8:45 am]
BILLING CODE 6560-50-P