Pendimethalin; Pesticide Tolerance, 61351-61354 [2024-16544]
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Federal Register / Vol. 89, No. 147 / Wednesday, July 31, 2024 / Rules and Regulations
ENVIRONMENTAL PROTECTION
AGENCY
40 CFR Part 180
[EPA–HQ–OPP–2023–0308; FRL–12049–01–
OCSPP]
Pendimethalin; Pesticide Tolerance
Environmental Protection
Agency (EPA).
ACTION: Final rule.
AGENCY:
B. How can I get electronic access to
other related information?
This regulation establishes
tolerances for residues of pendimethalin
in or on fig and fig, dried. BASF
Corporation has requested these
tolerances under the Federal Food,
Drug, and Cosmetic Act (FFDCA).
DATES: This regulation is effective July
31, 2024. Objections and requests for
hearings must be received on or before
September 30, 2024 and must be filed in
accordance with the instructions
provided in 40 CFR part 178 (see also
Unit I.C. of the SUPPLEMENTARY
INFORMATION).
SUMMARY:
The docket for this action,
identified by docket identification (ID)
number EPA–HQ–OPP–2023–0308, is
available at https://www.regulations.gov
or at the Office of Pesticide Programs
Regulatory Public Docket (OPP Docket)
in the Environmental Protection Agency
Docket Center (EPA/DC), West William
Jefferson Clinton Bldg., Rm. 3334, 1301
Constitution Ave. NW, Washington, DC
20460–0001. The Public Reading Room
is open from 8:30 a.m. to 4:30 p.m.,
Monday through Friday, excluding legal
holidays. The telephone number for the
Public Reading Room, and for the OPP
Docket is (202) 566–1744. Please review
the visitor instructions and additional
information about the docket available
at https://www.epa.gov/dockets.
FOR FURTHER INFORMATION CONTACT:
Charles Smith, Director, Registration
Division (7505T), Office of Pesticide
Programs, Environmental Protection
Agency, 1200 Pennsylvania Ave. NW,
Washington, DC 20460–0001; main
telephone number: (202) 566–1030;
email address: RDFRNotices@epa.gov.
SUPPLEMENTARY INFORMATION:
ADDRESSES:
I. General Information
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A. Does this action apply to me?
You may be potentially affected by
this action if you are an agricultural
producer, food manufacturer, or
pesticide manufacturer. The following
list of North American Industrial
Classification System (NAICS) codes is
not intended to be exhaustive, but rather
provides a guide to help readers
determine whether this document
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applies to them. Potentially affected
entities may include:
• Crop production (NAICS code 111).
• Animal production (NAICS code
112).
• Food manufacturing (NAICS code
311).
• Pesticide manufacturing (NAICS
code 32532).
You may access a frequently updated
electronic version of EPA’s tolerance
regulations at 40 CFR part 180 through
the Office of the Federal Register’s eCFR site at https://www.ecfr.gov/
current/title-40.
C. How can I file an objection or hearing
request?
Under FFDCA section 408(g), 21
U.S.C. 346a(g), any person may file an
objection to any aspect of this regulation
and may also request a hearing on those
objections. You must file your objection
or request a hearing on this regulation
in accordance with the instructions
provided in 40 CFR part 178. To ensure
proper receipt by EPA, you must
identify docket ID number EPA–HQ–
OPP–2023–0308, in the subject line on
the first page of your submission. All
objections and requests for a hearing
must be in writing and must be received
by the Hearing Clerk on or before
September 30, 2024. Addresses for mail
and hand delivery of objections and
hearing requests are provided in 40 CFR
178.25(b).
In addition to filing an objection or
hearing request with the Hearing Clerk
as described in 40 CFR part 178, please
submit a copy of the filing (excluding
any Confidential Business Information
(CBI)) for inclusion in the public docket.
Information not marked confidential
pursuant to 40 CFR part 2 may be
disclosed publicly by EPA without prior
notice. Submit the non-CBI copy of your
objection or hearing request, identified
by docket ID number EPA–HQ–OPP–
2023–0308, by one of the following
methods:
• Federal eRulemaking Portal:
https://www.regulations.gov. Follow the
online instructions for submitting
comments. Do not submit electronically
any information you consider to be CBI
or other information whose disclosure is
restricted by statute.
• Mail: OPP Docket, Environmental
Protection Agency Docket Center (EPA/
DC), (28221T), 1200 Pennsylvania Ave.
NW, Washington, DC 20460–0001.
Additional instructions on
commenting or visiting the docket,
along with more information about
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61351
dockets generally, is available at https://
www.epa.gov/dockets.
• Hand Delivery: To make special
arrangements for hand delivery or
delivery of boxed information, please
follow the instructions at https://
www.epa.gov/dockets/where-sendcomments-epa-dockets.
II. Summary of Petitioned-For
Tolerance
In the Federal Register of December
19, 2023 (88 FR 87733) (FRL–10579–11),
EPA issued a document pursuant to
FFDCA section 408(d)(3), 21 U.S.C.
346a(d)(3), announcing the filing of a
pesticide petition (PP 2F9038) by BASF
Corporation, 26 Davis Drive, Research
Triangle Park, NC 27709. The petition
requested that 40 CFR part 180 be
amended by establishing tolerances for
residues of the herbicide pendimethalin,
including its metabolites and
degradates, in or on the raw agricultural
commodities fig at 0.1 parts per million
(ppm) and fig, dried at 3.0 ppm. That
document referenced a summary of the
petition prepared by BASF, the
registrant, which is available in the
docket at https://www.regulations.gov.
The December 19, 2023, notice of
filing supersedes a notice of filing
published in the Federal Register of
July 26, 2023 (88 FR 48179) (FRL–
10579–06), which was based on an
earlier version of the same petition
(2F9038) requesting tolerances for
tropical and subtropical fruit, medium
to large fruit, edible peel subgroup 23B
at 0.1 ppm and fig, dried fruit at 3.0
ppm; and an inadvertent tolerance for
cilantro, fresh leaves at 0.1 ppm.
Following that July 2023 publication,
BASF amended its petition to request
tolerances only for fig and fig, dried, as
noticed in the December 2023
publication.
No comments were received in
response to the December 19, 2023, and
the July 26, 2023, notices of filing.
Based upon review of the data
supporting the petition and in
accordance with its authority under
FFDCA section 408(d)(4)(A)(i), EPA has
modified the level at which one of the
tolerances is being established. The
reason for this change is explained in
Unit IV.D.
III. Aggregate Risk Assessment and
Determination of Safety
Section 408(b)(2)(A)(i) of FFDCA
allows EPA to establish a tolerance (the
legal limit for a pesticide chemical
residue in or on a food) only if EPA
determines that the tolerance is ‘‘safe.’’
Section 408(b)(2)(A)(ii) of FFDCA
defines ‘‘safe’’ to mean that ‘‘there is a
reasonable certainty that no harm will
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result from aggregate exposure to the
pesticide chemical residue, including
all anticipated dietary exposures and all
other exposures for which there is
reliable information.’’ This includes
exposure through drinking water and in
residential settings but does not include
occupational exposure. Section
408(b)(2)(C) of FFDCA requires EPA to
give special consideration to exposure
of infants and children to the pesticide
chemical residue in establishing a
tolerance and to ‘‘ensure that there is a
reasonable certainty that no harm will
result to infants and children from
aggregate exposure to the pesticide
chemical residue . . . .’’
Consistent with FFDCA section
408(b)(2)(D), and the factors specified
therein, EPA has reviewed the available
scientific data and other relevant
information in support of this action.
EPA has sufficient data to assess the
hazards of and to make a determination
on aggregate exposure for
pendimethalin including exposure
resulting from the tolerances established
by this action. EPA’s assessment of
exposures and risks associated with
pendimethalin follows.
In an effort to streamline its
publications in the Federal Register,
EPA is not reprinting sections that
repeat what has been previously
published for tolerance rulemakings for
the same pesticide chemical. Where
scientific information concerning a
particular chemical remains unchanged,
the content of those sections would not
vary between tolerance rulemakings,
and EPA considers referral back to those
sections as sufficient to provide an
explanation of the information EPA
considered in making its safety
determination for the new rulemaking.
In the Federal Register of February
16, 2018 (83 FR 6975) (FRL–9973–03)
and October 25, 2019 (84 FR 57336)
(FRL–10000–06), EPA published
tolerance rulemakings for
pendimethalin in which EPA
concluded, based on the available
information, that there is a reasonable
certainty that no harm would result
from aggregate exposure to
pendimethalin and established
tolerances for residues of that chemical.
EPA is incorporating previously
published sections from these
rulemakings as described further in this
rulemaking, as they remain unchanged.
Toxicological profile. For a discussion
of the Toxicological Profile of
pendimethalin, see Unit III.A. of the
October 25, 2019, rulemaking.
Toxicological points of departure/
Levels of concern. For a summary of the
Toxicological Points of Departure/
Levels of Concern for pendimethalin
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used for human health risk assessment,
please reference Unit III.B. of the
February 16, 2018, rulemaking.
Exposure assessment. Much of the
exposure assessment for pendimethalin
remains unchanged from the discussion
in Unit III.C. of the October 25, 2019,
rulemaking, except as described below.
Dietary exposure from food and feed
uses. EPA’s dietary exposure
assessments have been updated to
include the additional exposure from
the proposed new uses on fresh and
dried fig. The acute and chronic dietary
(food and drinking water) exposure
assessments in support of the proposed
fresh and dried fig uses were conducted
using the Dietary Exposure Evaluation
Model software with the Food
Commodity Intake Database (DEEM–
FCID) Version 4.02. This software uses
2005–2010 food consumption data from
the United States Department of
Agriculture’s (USDA’s) National Health
and Nutrition Examination Survey,
What We Eat in America (NHANES/
WWEIA). The unrefined acute and
chronic dietary exposure assessments
assumed 100 percent crop treated (PCT),
tolerance-level residues for all crops,
and maximum anticipated residues to
address all residues of concern in
ruminant commodities.
Drinking water and non-occupational
exposures. The drinking water numbers
have not changed as a result of the
proposed fresh and dried fig uses. For
a detailed summary of the drinking
water analysis for pendimethalin used
for the human health risk assessment,
please reference Unit III.C.2. of the
October 25, 2019, rulemaking.
There are no residential exposures
expected from the currently proposed
uses; however, pendimethalin is
currently registered for residential usage
on gardens, golf course turf, lawns, and
ornamentals. The highest anticipated
short-term aggregate exposure scenarios
for children and adults did not present
risks of concern (i.e., margins of
exposure (MOEs) are > the level of
concern (LOC) of 30). Intermediate-term
exposures to pendimethalin are not
likely because of the intermittent nature
of applications by homeowners (e.g.,
garden sprays). Long-term aggregate
exposure is not anticipated for
residential uses.
Cumulative exposure. Section
408(b)(2)(D)(v) of FFDCA requires that,
when considering whether to establish,
modify, or revoke a tolerance, the
Agency consider ‘‘available
information’’ concerning the cumulative
effects of a particular pesticide’s
residues and ‘‘other substances that
have a common mechanism of toxicity
The Agency has utilized this framework
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for pendimethalin and determined that
although pendimethalin shares some
chemical and/or toxicological
characteristics (e.g., chemical structure
or apical endpoint) with other
pesticides, the toxicological database
does not support a testable hypothesis
for a common mechanism of action. No
further data are required to determine
that no common mechanism of toxicity
exists for pendimethalin, and other
pesticides and no further cumulative
evaluation is necessary for
pendimethalin.
Safety factor for infants and children.
EPA continues to conclude that there
are reliable data to support the
reduction of the Food Quality Protection
Act (FQPA) safety factor from 10X to
1X. See Unit III.D. of the October 25,
2019, rulemaking for a discussion of the
Agency’s rationale for that
determination.
Aggregate risks and determination of
safety. EPA determines whether acute
and chronic dietary pesticide exposures
are safe by comparing aggregate
exposure estimates to the acute
population adjusted dose (aPAD) and
chronic population adjusted dose
(cPAD). For linear cancer risks, EPA
calculates the lifetime probability of
acquiring cancer given the estimated
aggregate exposure. Short-,
intermediate-, and chronic-term risks
are evaluated by comparing the
estimated aggregate food, water, and
residential exposure to the appropriate
points of departure (PODs) to ensure
that an adequate MOE exists.
The results of the acute dietary
analysis for food and drinking water at
the 95th percentile of exposure shows
that the acute dietary risk estimates are
below the Agency’s level of concern
(<100% of the aPAD) for all population
subgroups and were estimated at <1% of
the aPAD for the U.S. general
population and 2.1% of the aPAD for
the most highly exposed population
subgroup (infants <1 years old). The
results of the chronic dietary analysis
for food and drinking water indicate
that the chronic dietary risk estimates
are below the Agency’s level of concern
(<100% of the cPAD) for all population
subgroups and were estimated at <1% of
the cPAD for the U.S. general
population and 2.3% of the cPAD for
the most highly exposed population
subgroup (children 1 to 2 years old).
Acute aggregate exposure is
anticipated to occur from dietary
exposure in food and drinking water
only. There are no risks of concern for
acute dietary exposure and thus no risks
of concern for acute aggregate exposure.
Short-term aggregate risk assessment
was performed since there is potential
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for post-application exposure from the
existing uses in residential settings. The
highest anticipated short-term aggregate
exposure scenarios for children and
adults did not present risks of concern
(i.e., MOEs are >LOC of 30).
Intermediate-term exposures to
pendimethalin are not likely because of
the intermittent nature of applications
by homeowners (e.g., garden sprays).
Long-term aggregate exposure is not
anticipated for residential uses.
Therefore, chronic aggregate risk
estimates for pendimethalin include
food and drinking water only, and are
equivalent to the chronic dietary risk
estimates, and are below HED’s LOC.
Pendimethalin is classified as a
‘‘possible human carcinogen.’’ However,
the chronic dietary risk assessment is
considered to be protective of any
cancer effects; therefore, a separate
quantitative cancer dietary risk
assessment is not required. The chronic
reference dose (cRfD)/cPAD is
considered to be protective of all
chronic toxicity, including
carcinogenicity, that could result from
exposure to pendimethalin. Since there
are no chronic aggregate risks of
concern, there are no cancer aggregate
risks of concern.
Therefore, based on the risk
assessments and information described
above, EPA concludes there is a
reasonable certainty that no harm will
result to the general population, or to
infants and children, from aggregate
exposure to pendimethalin residues.
More detailed information on the
subject action to establish tolerances in
or on fig commodities can be found in
the document titled ‘‘Pendimethalin—
Human Health Risk Assessment to
Support the Proposed New Use on Fig.’’
available at https://www.regulations.gov
in docket ID number EPA–HQ–OPP–
2023–0308.
IV. Other Considerations
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A. Analytical Enforcement Methodology
Adequate analytical enforcement
methodology, gas chromatography with
electron capture detection (GC/ECD), is
available to enforce the tolerance
expression. The method may be
requested from: Chief, Analytical
Chemistry Branch, Environmental
Science Center, 701 Mapes Rd., Ft.
Meade, MD 20755–5350; telephone
number: (410) 305–2905; email address:
residuemethods@epa.gov.
B. International Residue Limits
In making its tolerance decisions, EPA
seeks to harmonize U.S. tolerances with
international standards whenever
possible, consistent with U.S. food
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safety standards and agricultural
practices. EPA considers the
international maximum residue limits
(MRLs) established by the Codex
Alimentarius Commission (Codex), as
required by FFDCA section 408(b)(4).
Codex Alimentarius is a joint United
Nations Food and Agriculture
Organization/World Health
Organization food standards program,
and it is recognized as an international
food safety standards-setting
organization in trade agreements to
which the United States is a party. EPA
may establish a tolerance that is
different from a Codex MRL; however,
FFDCA section 408(b)(4) requires that
EPA explain the reasons for departing
from the Codex level. The Codex has not
established any MRLs for pendimethalin
for the crops covered by this action.
C. Revisions to Petitioned-For
Tolerances
EPA is establishing the tolerance for
fig, dried at 3 ppm rather than 3.0 ppm
to be consistent with Organisation for
Economic Cooperation and
Development (OECD) rounding class
practices.
V. Conclusion
Therefore, tolerances are established
for residues of pendimethalin in or on
the raw agricultural commodities fig at
0.1 parts per million (ppm) and fig,
dried at 3 ppm.
VI. Statutory and Executive Order
Reviews
This action establishes tolerances
under FFDCA section 408(d) in
response to a petition submitted to the
Agency. The Office of Management and
Budget (OMB) has exempted these types
of actions from review under Executive
Order 12866, entitled ‘‘Regulatory
Planning and Review’’ (58 FR 51735,
October 4, 1993). Because this action
has been exempted from review under
Executive Order 12866, this action is
not subject to Executive Order 13211,
entitled ‘‘Actions Concerning
Regulations That Significantly Affect
Energy Supply, Distribution, or Use’’ (66
FR 28355, May 22, 2001), or Executive
Order 13045, entitled ‘‘Protection of
Children from Environmental Health
Risks and Safety Risks’’ (62 FR 19885,
April 23, 1997). This action does not
contain any information collections
subject to OMB approval under the
Paperwork Reduction Act (PRA) (44
U.S.C. 3501 et seq.), nor does it require
any special considerations under
Executive Order 12898, entitled
‘‘Federal Actions to Address
Environmental Justice in Minority
Populations and Low-Income
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61353
Populations’’ (59 FR 7629, February 16,
1994).
Since tolerances and exemptions that
are established on the basis of a petition
under FFDCA section 408(d), such as
the tolerances in this final rule, do not
require the issuance of a proposed rule,
the requirements of the Regulatory
Flexibility Act (RFA) (5 U.S.C. 601 et
seq.), do not apply.
This action directly regulates growers,
food processors, food handlers, and food
retailers, not States or Tribes, nor does
this action alter the relationships or
distribution of power and
responsibilities established by Congress
in the preemption provisions of FFDCA
section 408(n)(4). As such, the Agency
has determined that this action will not
have a substantial direct effect on States
or Tribal governments, on the
relationship between the National
Government and the States or Tribal
governments, or on the distribution of
power and responsibilities among the
various levels of government or between
the Federal Government and Indian
tribes. Thus, the Agency has determined
that Executive Order 13132, entitled
‘‘Federalism’’ (64 FR 43255, August 10,
1999), and Executive Order 13175,
entitled ‘‘Consultation and Coordination
with Indian Tribal Governments’’ (65 FR
67249, November 9, 2000), do not apply
to this action. In addition, this action
does not impose any enforceable duty or
contain any unfunded mandate as
described under Title II of the Unfunded
Mandates Reform Act (UMRA) (2 U.S.C.
1501 et seq.).
This action does not involve any
technical standards that would require
Agency consideration of voluntary
consensus standards pursuant to section
12(d) of the National Technology
Transfer and Advancement Act
(NTTAA) (15 U.S.C. 272 note).
VII. Congressional Review Act
Pursuant to the Congressional Review
Act (5 U.S.C. 801 et seq.), EPA will
submit a report containing this rule and
other required information to the U.S.
Senate, the U.S. House of
Representatives, and the Comptroller
General of the United States prior to
publication of the rule in the Federal
Register. This action is not a ‘‘major
rule’’ as defined by 5 U.S.C. 804(2).
List of Subjects in 40 CFR Part 180
Environmental protection,
Administrative practice and procedure,
Agricultural commodities, Pesticides,
and pests, Reporting and recordkeeping
requirements.
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Dated: July 19, 2024.
Charles Smith,
Director, Registration Division, Office of
Pesticide Programs.
behalf of its wholly owned subsidiary,
Multimedia, filed comments in support
of the Petition, as required by the
Commission’s rules (rules), reaffirming
Therefore, for the reasons stated in the Multimedia’s commitment to apply for
channel 33 and, if authorized, to
preamble, EPA is amending 40 CFR
promptly implement the facilities
chapter I as follows:
modifications necessary for the Station
to operate on channel 33.
PART 180—TOLERANCES AND
EXEMPTIONS FOR PESTICIDE
DATES: Effective July 31, 2024.
CHEMICAL RESIDUES IN FOOD
FOR FURTHER INFORMATION CONTACT:
Joyce Bernstein, Media Bureau, at (202)
■ 1. The authority citation for part 180
418–1647 or Joyce.Bernstein@fcc.gov, or
continues to read as follows:
Mark Colombo, Media Bureau, at (202)
Authority: 21 U.S.C. 321(q), 346a and 371.
418–7611 or Mark.Colombo@fcc.gov.
SUPPLEMENTARY INFORMATION: The
■ 2. In § 180.361, amend paragraph
proposed rule was published at 89 FR
(a)(1) by designating the table as ‘‘Table
31125 on April 24, 2024. The Petitioner
1 to Paragraph (a)(1)’’ and adding to
filed comments in support of the
newly designated table 1, in
alphabetical order, the entries ‘‘Fig’’ and petition reaffirming its commitment to
apply for channel 33. No other
‘‘Fig, dried’’ to read as follows:
comments were filed.
§ 180.361 Pendimethalin; tolerances for
The Bureau believes the public
residues.
interest would be served by substituting
(a) * * *
channel 33 for channel 13 at
(1) * * *
Jacksonville. According to the
Petitioner, the Station has received
TABLE 1 TO PARAGRAPH (a)(1)
persistent reception complaints from
viewers, many of whom state that they
Parts per
can receive signals from other local
Commodity
million
stations on UHF channels, but not
WTLV on VHF channel 13. The
Petitioner states that the Commission
*
*
*
*
*
Fig .............................................
0.1 has recognized that VHF channels have
Fig, dried ...................................
3 certain characteristics that pose
challenges for their use in providing
*
*
*
*
*
digital television service, including
propagation characteristics that allow
*
*
*
*
*
undesired signals and noise to be
[FR Doc. 2024–16544 Filed 7–30–24; 8:45 am]
receivable at relatively far distances,
BILLING CODE 6560–50–P
and that although VHF reception issues
are not universal, ‘‘environmental noise
blockages affecting [VHF] signal
FEDERAL COMMUNICATIONS
strength and reception exist’’ and
COMMISSION
‘‘[vary] widely from service area to
service area. Additionally, the Petitioner
47 CFR Part 73
notes that the Commission has observed
[MB Docket No. 24–112; RM–11981; DA 24–
the large variability in the performance
720; FR ID 235234]
of indoor antennas available to
consumers, with most antennas
Television Broadcasting Services
receiving ‘‘fairly well at UHF and . . .
Jacksonville, Florida
not so well to very poor at high-VHF.’’
WTLV is an NBC network affiliate and
AGENCY: Federal Communications
while an analysis provided by the
Commission.
Petitioner indicates that the Station’s
ACTION: Final rule.
move to channel 33 will result in
SUMMARY: The Video Division, Media
274,303 persons no longer being located
Bureau (Bureau), has before it a Notice
within the Station’s noise limited
of Proposed Rulemaking issued in
service contour (NLSC), all but 16,737
response to a Petition for Rulemaking
persons in the predicted loss area are
filed by Multimedia Holdings
within the NLSC of three other NBC
Corporation (Petitioner or Multimedia),
affiliated TV stations. Further, when the
the licensee of WTLV (Station or
Commission’s TVStudy software is run
WTLV), channel 13, Jacksonville,
for the Station’s licensed and proposed
Florida (Jacksonville). The Petitioner
facility with the ‘‘Study Area Mode’’ set
has requested the substitution of UHF
to ‘‘unrestricted’’ to predict coverage
channel 33 for VHF channel 13 in the
outside the proposed channel 33 NLSC,
Table of TV Allotments. TEGNA Inc., on all viewers in the remaining predicted
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loss area would continue to receive
over-the-air NBC network programming
from WTLV on channel 33. Thus, once
service provided by other NBC stations
and the terrain-limited coverage
predictions are taken into account, we
find that the proposed channel 33
facility will result in no loss of NBC
service to existing viewers within the
Station’s current NLSC.
We also find that the proposal
complies with all relevant technical
requirements for amendment of the
Table of TV Allotments, including the
interference protection requirements of
§ 73.622(a) of the rules, and further
demonstrates that the proposed channel
33 facility will provide full principal
community coverage to Jacksonville as
required by § 73.618 of the rules. In fact,
this channel substitution from VHF to
UHF will help improve service to
existing viewers, including those in the
Station’s principal community of
license, by eliminating reception issues
related to the Station’s current operation
on a high-VHF channel. As proposed,
channel 33 can be substituted for
channel 13 at Jacksonville in
compliance with the principal
community coverage requirements of
§ 73.618(a) of the rules, at coordinates
30–16′–25″ N. and 81–33′–12″ W. In
addition, we find that this channel
change meets the technical
requirements set forth in § 73.622(a) of
the rules.
This is a synopsis of the
Commission’s Report and Order, MB
Docket No. 24–112; RM–11981; DA 24–
720, adopted July 24, 2024, and released
July 24, 2024. The full text of this
document is available for download at
https://www.fcc.gov/edocs. To request
materials in accessible formats for
people with disabilities (braille, large
print, electronic files, audio format),
send an email to fcc504@fcc.gov or call
the Consumer & Governmental Affairs
Bureau at 202–418–0530 (voice), 202–
418–0432 (tty).
This document does not contain
information collection requirements
subject to the Paperwork Reduction Act
of 1995, Public Law 104–13. In addition,
therefore, it does not contain any
proposed information collection burden
‘‘for small business concerns with fewer
than 25 employees,’’ pursuant to the
Small Business Paperwork Relief Act of
2002, Public Law 107–198, see 44 U.S.C.
3506(c)(4). Provisions of the Regulatory
Flexibility Act of 1980, 5 U.S.C. 601–
612, do not apply to this proceeding.
The Commission will send a copy of
the Report and Order in a report to be
sent to Congress and the Government
Accountability Office pursuant to the
E:\FR\FM\31JYR1.SGM
31JYR1
Agencies
[Federal Register Volume 89, Number 147 (Wednesday, July 31, 2024)]
[Rules and Regulations]
[Pages 61351-61354]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2024-16544]
[[Page 61351]]
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ENVIRONMENTAL PROTECTION AGENCY
40 CFR Part 180
[EPA-HQ-OPP-2023-0308; FRL-12049-01-OCSPP]
Pendimethalin; Pesticide Tolerance
AGENCY: Environmental Protection Agency (EPA).
ACTION: Final rule.
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SUMMARY: This regulation establishes tolerances for residues of
pendimethalin in or on fig and fig, dried. BASF Corporation has
requested these tolerances under the Federal Food, Drug, and Cosmetic
Act (FFDCA).
DATES: This regulation is effective July 31, 2024. Objections and
requests for hearings must be received on or before September 30, 2024
and must be filed in accordance with the instructions provided in 40
CFR part 178 (see also Unit I.C. of the SUPPLEMENTARY INFORMATION).
ADDRESSES: The docket for this action, identified by docket
identification (ID) number EPA-HQ-OPP-2023-0308, is available at
https://www.regulations.gov or at the Office of Pesticide Programs
Regulatory Public Docket (OPP Docket) in the Environmental Protection
Agency Docket Center (EPA/DC), West William Jefferson Clinton Bldg.,
Rm. 3334, 1301 Constitution Ave. NW, Washington, DC 20460-0001. The
Public Reading Room is open from 8:30 a.m. to 4:30 p.m., Monday through
Friday, excluding legal holidays. The telephone number for the Public
Reading Room, and for the OPP Docket is (202) 566-1744. Please review
the visitor instructions and additional information about the docket
available at https://www.epa.gov/dockets.
FOR FURTHER INFORMATION CONTACT: Charles Smith, Director, Registration
Division (7505T), Office of Pesticide Programs, Environmental
Protection Agency, 1200 Pennsylvania Ave. NW, Washington, DC 20460-
0001; main telephone number: (202) 566-1030; email address:
[email protected].
SUPPLEMENTARY INFORMATION:
I. General Information
A. Does this action apply to me?
You may be potentially affected by this action if you are an
agricultural producer, food manufacturer, or pesticide manufacturer.
The following list of North American Industrial Classification System
(NAICS) codes is not intended to be exhaustive, but rather provides a
guide to help readers determine whether this document applies to them.
Potentially affected entities may include:
Crop production (NAICS code 111).
Animal production (NAICS code 112).
Food manufacturing (NAICS code 311).
Pesticide manufacturing (NAICS code 32532).
B. How can I get electronic access to other related information?
You may access a frequently updated electronic version of EPA's
tolerance regulations at 40 CFR part 180 through the Office of the
Federal Register's e-CFR site at https://www.ecfr.gov/current/title-40.
C. How can I file an objection or hearing request?
Under FFDCA section 408(g), 21 U.S.C. 346a(g), any person may file
an objection to any aspect of this regulation and may also request a
hearing on those objections. You must file your objection or request a
hearing on this regulation in accordance with the instructions provided
in 40 CFR part 178. To ensure proper receipt by EPA, you must identify
docket ID number EPA-HQ-OPP-2023-0308, in the subject line on the first
page of your submission. All objections and requests for a hearing must
be in writing and must be received by the Hearing Clerk on or before
September 30, 2024. Addresses for mail and hand delivery of objections
and hearing requests are provided in 40 CFR 178.25(b).
In addition to filing an objection or hearing request with the
Hearing Clerk as described in 40 CFR part 178, please submit a copy of
the filing (excluding any Confidential Business Information (CBI)) for
inclusion in the public docket. Information not marked confidential
pursuant to 40 CFR part 2 may be disclosed publicly by EPA without
prior notice. Submit the non-CBI copy of your objection or hearing
request, identified by docket ID number EPA-HQ-OPP-2023-0308, by one of
the following methods:
Federal eRulemaking Portal: https://www.regulations.gov.
Follow the online instructions for submitting comments. Do not submit
electronically any information you consider to be CBI or other
information whose disclosure is restricted by statute.
Mail: OPP Docket, Environmental Protection Agency Docket
Center (EPA/DC), (28221T), 1200 Pennsylvania Ave. NW, Washington, DC
20460-0001.
Additional instructions on commenting or visiting the docket, along
with more information about dockets generally, is available at https://www.epa.gov/dockets.
Hand Delivery: To make special arrangements for hand
delivery or delivery of boxed information, please follow the
instructions at https://www.epa.gov/dockets/where-send-comments-epa-dockets.
II. Summary of Petitioned-For Tolerance
In the Federal Register of December 19, 2023 (88 FR 87733) (FRL-
10579-11), EPA issued a document pursuant to FFDCA section 408(d)(3),
21 U.S.C. 346a(d)(3), announcing the filing of a pesticide petition (PP
2F9038) by BASF Corporation, 26 Davis Drive, Research Triangle Park, NC
27709. The petition requested that 40 CFR part 180 be amended by
establishing tolerances for residues of the herbicide pendimethalin,
including its metabolites and degradates, in or on the raw agricultural
commodities fig at 0.1 parts per million (ppm) and fig, dried at 3.0
ppm. That document referenced a summary of the petition prepared by
BASF, the registrant, which is available in the docket at https://www.regulations.gov.
The December 19, 2023, notice of filing supersedes a notice of
filing published in the Federal Register of July 26, 2023 (88 FR 48179)
(FRL-10579-06), which was based on an earlier version of the same
petition (2F9038) requesting tolerances for tropical and subtropical
fruit, medium to large fruit, edible peel subgroup 23B at 0.1 ppm and
fig, dried fruit at 3.0 ppm; and an inadvertent tolerance for cilantro,
fresh leaves at 0.1 ppm. Following that July 2023 publication, BASF
amended its petition to request tolerances only for fig and fig, dried,
as noticed in the December 2023 publication.
No comments were received in response to the December 19, 2023, and
the July 26, 2023, notices of filing.
Based upon review of the data supporting the petition and in
accordance with its authority under FFDCA section 408(d)(4)(A)(i), EPA
has modified the level at which one of the tolerances is being
established. The reason for this change is explained in Unit IV.D.
III. Aggregate Risk Assessment and Determination of Safety
Section 408(b)(2)(A)(i) of FFDCA allows EPA to establish a
tolerance (the legal limit for a pesticide chemical residue in or on a
food) only if EPA determines that the tolerance is ``safe.'' Section
408(b)(2)(A)(ii) of FFDCA defines ``safe'' to mean that ``there is a
reasonable certainty that no harm will
[[Page 61352]]
result from aggregate exposure to the pesticide chemical residue,
including all anticipated dietary exposures and all other exposures for
which there is reliable information.'' This includes exposure through
drinking water and in residential settings but does not include
occupational exposure. Section 408(b)(2)(C) of FFDCA requires EPA to
give special consideration to exposure of infants and children to the
pesticide chemical residue in establishing a tolerance and to ``ensure
that there is a reasonable certainty that no harm will result to
infants and children from aggregate exposure to the pesticide chemical
residue . . . .''
Consistent with FFDCA section 408(b)(2)(D), and the factors
specified therein, EPA has reviewed the available scientific data and
other relevant information in support of this action. EPA has
sufficient data to assess the hazards of and to make a determination on
aggregate exposure for pendimethalin including exposure resulting from
the tolerances established by this action. EPA's assessment of
exposures and risks associated with pendimethalin follows.
In an effort to streamline its publications in the Federal
Register, EPA is not reprinting sections that repeat what has been
previously published for tolerance rulemakings for the same pesticide
chemical. Where scientific information concerning a particular chemical
remains unchanged, the content of those sections would not vary between
tolerance rulemakings, and EPA considers referral back to those
sections as sufficient to provide an explanation of the information EPA
considered in making its safety determination for the new rulemaking.
In the Federal Register of February 16, 2018 (83 FR 6975) (FRL-
9973-03) and October 25, 2019 (84 FR 57336) (FRL-10000-06), EPA
published tolerance rulemakings for pendimethalin in which EPA
concluded, based on the available information, that there is a
reasonable certainty that no harm would result from aggregate exposure
to pendimethalin and established tolerances for residues of that
chemical. EPA is incorporating previously published sections from these
rulemakings as described further in this rulemaking, as they remain
unchanged.
Toxicological profile. For a discussion of the Toxicological
Profile of pendimethalin, see Unit III.A. of the October 25, 2019,
rulemaking.
Toxicological points of departure/Levels of concern. For a summary
of the Toxicological Points of Departure/Levels of Concern for
pendimethalin used for human health risk assessment, please reference
Unit III.B. of the February 16, 2018, rulemaking.
Exposure assessment. Much of the exposure assessment for
pendimethalin remains unchanged from the discussion in Unit III.C. of
the October 25, 2019, rulemaking, except as described below.
Dietary exposure from food and feed uses. EPA's dietary exposure
assessments have been updated to include the additional exposure from
the proposed new uses on fresh and dried fig. The acute and chronic
dietary (food and drinking water) exposure assessments in support of
the proposed fresh and dried fig uses were conducted using the Dietary
Exposure Evaluation Model software with the Food Commodity Intake
Database (DEEM-FCID) Version 4.02. This software uses 2005-2010 food
consumption data from the United States Department of Agriculture's
(USDA's) National Health and Nutrition Examination Survey, What We Eat
in America (NHANES/WWEIA). The unrefined acute and chronic dietary
exposure assessments assumed 100 percent crop treated (PCT), tolerance-
level residues for all crops, and maximum anticipated residues to
address all residues of concern in ruminant commodities.
Drinking water and non-occupational exposures. The drinking water
numbers have not changed as a result of the proposed fresh and dried
fig uses. For a detailed summary of the drinking water analysis for
pendimethalin used for the human health risk assessment, please
reference Unit III.C.2. of the October 25, 2019, rulemaking.
There are no residential exposures expected from the currently
proposed uses; however, pendimethalin is currently registered for
residential usage on gardens, golf course turf, lawns, and ornamentals.
The highest anticipated short-term aggregate exposure scenarios for
children and adults did not present risks of concern (i.e., margins of
exposure (MOEs) are > the level of concern (LOC) of 30). Intermediate-
term exposures to pendimethalin are not likely because of the
intermittent nature of applications by homeowners (e.g., garden
sprays). Long-term aggregate exposure is not anticipated for
residential uses.
Cumulative exposure. Section 408(b)(2)(D)(v) of FFDCA requires
that, when considering whether to establish, modify, or revoke a
tolerance, the Agency consider ``available information'' concerning the
cumulative effects of a particular pesticide's residues and ``other
substances that have a common mechanism of toxicity The Agency has
utilized this framework for pendimethalin and determined that although
pendimethalin shares some chemical and/or toxicological characteristics
(e.g., chemical structure or apical endpoint) with other pesticides,
the toxicological database does not support a testable hypothesis for a
common mechanism of action. No further data are required to determine
that no common mechanism of toxicity exists for pendimethalin, and
other pesticides and no further cumulative evaluation is necessary for
pendimethalin.
Safety factor for infants and children. EPA continues to conclude
that there are reliable data to support the reduction of the Food
Quality Protection Act (FQPA) safety factor from 10X to 1X. See Unit
III.D. of the October 25, 2019, rulemaking for a discussion of the
Agency's rationale for that determination.
Aggregate risks and determination of safety. EPA determines whether
acute and chronic dietary pesticide exposures are safe by comparing
aggregate exposure estimates to the acute population adjusted dose
(aPAD) and chronic population adjusted dose (cPAD). For linear cancer
risks, EPA calculates the lifetime probability of acquiring cancer
given the estimated aggregate exposure. Short-, intermediate-, and
chronic-term risks are evaluated by comparing the estimated aggregate
food, water, and residential exposure to the appropriate points of
departure (PODs) to ensure that an adequate MOE exists.
The results of the acute dietary analysis for food and drinking
water at the 95th percentile of exposure shows that the acute dietary
risk estimates are below the Agency's level of concern (<100% of the
aPAD) for all population subgroups and were estimated at <1% of the
aPAD for the U.S. general population and 2.1% of the aPAD for the most
highly exposed population subgroup (infants <1 years old). The results
of the chronic dietary analysis for food and drinking water indicate
that the chronic dietary risk estimates are below the Agency's level of
concern (<100% of the cPAD) for all population subgroups and were
estimated at <1% of the cPAD for the U.S. general population and 2.3%
of the cPAD for the most highly exposed population subgroup (children 1
to 2 years old).
Acute aggregate exposure is anticipated to occur from dietary
exposure in food and drinking water only. There are no risks of concern
for acute dietary exposure and thus no risks of concern for acute
aggregate exposure. Short-term aggregate risk assessment was performed
since there is potential
[[Page 61353]]
for post-application exposure from the existing uses in residential
settings. The highest anticipated short-term aggregate exposure
scenarios for children and adults did not present risks of concern
(i.e., MOEs are >LOC of 30). Intermediate-term exposures to
pendimethalin are not likely because of the intermittent nature of
applications by homeowners (e.g., garden sprays). Long-term aggregate
exposure is not anticipated for residential uses. Therefore, chronic
aggregate risk estimates for pendimethalin include food and drinking
water only, and are equivalent to the chronic dietary risk estimates,
and are below HED's LOC. Pendimethalin is classified as a ``possible
human carcinogen.'' However, the chronic dietary risk assessment is
considered to be protective of any cancer effects; therefore, a
separate quantitative cancer dietary risk assessment is not required.
The chronic reference dose (cRfD)/cPAD is considered to be protective
of all chronic toxicity, including carcinogenicity, that could result
from exposure to pendimethalin. Since there are no chronic aggregate
risks of concern, there are no cancer aggregate risks of concern.
Therefore, based on the risk assessments and information described
above, EPA concludes there is a reasonable certainty that no harm will
result to the general population, or to infants and children, from
aggregate exposure to pendimethalin residues. More detailed information
on the subject action to establish tolerances in or on fig commodities
can be found in the document titled ``Pendimethalin--Human Health Risk
Assessment to Support the Proposed New Use on Fig.'' available at
https://www.regulations.gov in docket ID number EPA-HQ-OPP-2023-0308.
IV. Other Considerations
A. Analytical Enforcement Methodology
Adequate analytical enforcement methodology, gas chromatography
with electron capture detection (GC/ECD), is available to enforce the
tolerance expression. The method may be requested from: Chief,
Analytical Chemistry Branch, Environmental Science Center, 701 Mapes
Rd., Ft. Meade, MD 20755-5350; telephone number: (410) 305-2905; email
address: [email protected].
B. International Residue Limits
In making its tolerance decisions, EPA seeks to harmonize U.S.
tolerances with international standards whenever possible, consistent
with U.S. food safety standards and agricultural practices. EPA
considers the international maximum residue limits (MRLs) established
by the Codex Alimentarius Commission (Codex), as required by FFDCA
section 408(b)(4). Codex Alimentarius is a joint United Nations Food
and Agriculture Organization/World Health Organization food standards
program, and it is recognized as an international food safety
standards-setting organization in trade agreements to which the United
States is a party. EPA may establish a tolerance that is different from
a Codex MRL; however, FFDCA section 408(b)(4) requires that EPA explain
the reasons for departing from the Codex level. The Codex has not
established any MRLs for pendimethalin for the crops covered by this
action.
C. Revisions to Petitioned-For Tolerances
EPA is establishing the tolerance for fig, dried at 3 ppm rather
than 3.0 ppm to be consistent with Organisation for Economic
Cooperation and Development (OECD) rounding class practices.
V. Conclusion
Therefore, tolerances are established for residues of pendimethalin
in or on the raw agricultural commodities fig at 0.1 parts per million
(ppm) and fig, dried at 3 ppm.
VI. Statutory and Executive Order Reviews
This action establishes tolerances under FFDCA section 408(d) in
response to a petition submitted to the Agency. The Office of
Management and Budget (OMB) has exempted these types of actions from
review under Executive Order 12866, entitled ``Regulatory Planning and
Review'' (58 FR 51735, October 4, 1993). Because this action has been
exempted from review under Executive Order 12866, this action is not
subject to Executive Order 13211, entitled ``Actions Concerning
Regulations That Significantly Affect Energy Supply, Distribution, or
Use'' (66 FR 28355, May 22, 2001), or Executive Order 13045, entitled
``Protection of Children from Environmental Health Risks and Safety
Risks'' (62 FR 19885, April 23, 1997). This action does not contain any
information collections subject to OMB approval under the Paperwork
Reduction Act (PRA) (44 U.S.C. 3501 et seq.), nor does it require any
special considerations under Executive Order 12898, entitled ``Federal
Actions to Address Environmental Justice in Minority Populations and
Low-Income Populations'' (59 FR 7629, February 16, 1994).
Since tolerances and exemptions that are established on the basis
of a petition under FFDCA section 408(d), such as the tolerances in
this final rule, do not require the issuance of a proposed rule, the
requirements of the Regulatory Flexibility Act (RFA) (5 U.S.C. 601 et
seq.), do not apply.
This action directly regulates growers, food processors, food
handlers, and food retailers, not States or Tribes, nor does this
action alter the relationships or distribution of power and
responsibilities established by Congress in the preemption provisions
of FFDCA section 408(n)(4). As such, the Agency has determined that
this action will not have a substantial direct effect on States or
Tribal governments, on the relationship between the National Government
and the States or Tribal governments, or on the distribution of power
and responsibilities among the various levels of government or between
the Federal Government and Indian tribes. Thus, the Agency has
determined that Executive Order 13132, entitled ``Federalism'' (64 FR
43255, August 10, 1999), and Executive Order 13175, entitled
``Consultation and Coordination with Indian Tribal Governments'' (65 FR
67249, November 9, 2000), do not apply to this action. In addition,
this action does not impose any enforceable duty or contain any
unfunded mandate as described under Title II of the Unfunded Mandates
Reform Act (UMRA) (2 U.S.C. 1501 et seq.).
This action does not involve any technical standards that would
require Agency consideration of voluntary consensus standards pursuant
to section 12(d) of the National Technology Transfer and Advancement
Act (NTTAA) (15 U.S.C. 272 note).
VII. Congressional Review Act
Pursuant to the Congressional Review Act (5 U.S.C. 801 et seq.),
EPA will submit a report containing this rule and other required
information to the U.S. Senate, the U.S. House of Representatives, and
the Comptroller General of the United States prior to publication of
the rule in the Federal Register. This action is not a ``major rule''
as defined by 5 U.S.C. 804(2).
List of Subjects in 40 CFR Part 180
Environmental protection, Administrative practice and procedure,
Agricultural commodities, Pesticides, and pests, Reporting and
recordkeeping requirements.
[[Page 61354]]
Dated: July 19, 2024.
Charles Smith,
Director, Registration Division, Office of Pesticide Programs.
Therefore, for the reasons stated in the preamble, EPA is amending
40 CFR chapter I as follows:
PART 180--TOLERANCES AND EXEMPTIONS FOR PESTICIDE CHEMICAL RESIDUES
IN FOOD
0
1. The authority citation for part 180 continues to read as follows:
Authority: 21 U.S.C. 321(q), 346a and 371.
0
2. In Sec. 180.361, amend paragraph (a)(1) by designating the table as
``Table 1 to Paragraph (a)(1)'' and adding to newly designated table 1,
in alphabetical order, the entries ``Fig'' and ``Fig, dried'' to read
as follows:
Sec. 180.361 Pendimethalin; tolerances for residues.
(a) * * *
(1) * * *
Table 1 to Paragraph (a)(1)
------------------------------------------------------------------------
Parts per
Commodity million
------------------------------------------------------------------------
* * * * *
Fig........................................................ 0.1
Fig, dried................................................. 3
* * * * *
------------------------------------------------------------------------
* * * * *
[FR Doc. 2024-16544 Filed 7-30-24; 8:45 am]
BILLING CODE 6560-50-P