Tetraniliprole; Pesticide Tolerances, 42387-42390 [2024-10559]
Download as PDF
Federal Register / Vol. 89, No. 95 / Wednesday, May 15, 2024 / Rules and Regulations
TABLE 1 TO PARAGRAPH (a)
Parts per
million
Commodity
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0.4
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Grape, table 2 ..............................
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Herb, dried leaves, subgroup
25B ..........................................
Herb, fresh leaves, subgroup
25A ..........................................
Hop, dried cones ........................
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Mango 2 .......................................
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Olive 2 ..........................................
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Papaya ........................................
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Spice crop group 26 ...................
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Vegetable, legume, bean, edible
podded, subgroup 6–22A .......
Vegetable, legume, bean, succulent shelled, subgroup 6–
22C ..........................................
Vegetable, legume, forage and
hay, except soybean, subgroup 7–22A ...........................
Vegetable, legume, pea, edible
podded, subgroup 6–22B .......
Vegetable, legume, pea, succulent shelled, subgroup 6–
22D ..........................................
Vegetable, legume, pulse, bean,
dried shelled, except soybean,
subgroup 6–22E ......................
Vegetable, legume, pulse, pea,
dried shelled, subgroup 6–22F
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Environmental Protection
Agency (EPA).
2 ACTION: Final rule.
This regulation establishes
tolerance for residues of tetraniliprole in
or on tea, dried at 80 ppm. Bayer
150 CropScience LP requested this tolerance
under the Federal Food, Drug, and
40 Cosmetic Act (FFDCA).
70 DATES: This regulation is effective May
15, 2024. Objections and requests for
hearings must be received on or before
July 15, 2024 and must be filed in
0.7 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–2021–0624, is
1.5 available at https://www.regulations.gov
or at the Office of Pesticide Programs
Regulatory Public Docket (OPP Docket)
in the Environmental Protection Agency
80 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.,
2 Monday through Friday, excluding legal
holidays. The telephone number for the
Public Reading Room and the OPP
0.3
Docket is (202) 566–1744. Please review
the visitor instructions and additional
40 information about the docket available
at https://www.epa.gov/dockets.
2 FOR FURTHER INFORMATION CONTACT:
Charles Smith, Director, Registration
Division (7505T), Office of Pesticide
0.3 Programs, Environmental Protection
Agency, 1200 Pennsylvania Ave. NW,
Washington, DC 20460–0001; main
1
telephone number: (202) 566–1030;
1 email address: RDFRNotices@epa.gov.
SUPPLEMENTARY INFORMATION:
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[FR Doc. 2024–10490 Filed 5–14–24; 8:45 am]
BILLING CODE 6560–50–P
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ADDRESSES:
I. General Information
1 There are no U.S. registrations for these
commodities.
2 There are no U.S. registrations for these
commodities as of May 15, 2024.
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Tetraniliprole; Pesticide Tolerances
AGENCY:
3
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40 CFR Part 180
[EPA–HQ–OPP–2021–0624; FRL–11958–01–
OCSPP]
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Avocado 2 ....................................
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ENVIRONMENTAL PROTECTION
AGENCY
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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42387
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 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–2021–0624 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 July
15, 2024. Addresses for mail and hand
delivery of objections and hearing
requests are provided in 40 CFR
178.25(b).
EPA’s Office of Administrative Law
Judges (OALJ), in which the Hearing
Clerk is housed, urges parties to file and
serve documents by electronic means
only, notwithstanding any other
particular requirements set forth in
other procedural rules governing those
proceedings. See ‘‘Revised Order Urging
Electronic Service and Filing’’, dated
June 22, 2023, which can be found at
https://www.epa.gov/system/files/
documents/2023-06/2023-06-22%20%20revised%20order%20urging
%20electronic%20filing%20and
%20service.pdf.
Although EPA’s regulations require
submission via U.S. Mail or hand
delivery, EPA intends to treat
submissions filed via electronic means
as properly filed submissions; therefore,
EPA believes the preference for
submission via electronic means will
not be prejudicial. When submitting
documents to the OALJ electronically, a
person should utilize the OALJ e-filing
system at https://yosemite.epa.gov/oa/
eab/eab-alj_upload.nsf.
In addition to filing an objection or
hearing request with the Hearing Clerk
as described in 40 CFR part 178, please
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42388
Federal Register / Vol. 89, No. 95 / Wednesday, May 15, 2024 / Rules and Regulations
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–
2021–0624, 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
• 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.
Additional instructions on
commenting or visiting the docket,
along with more information about
dockets generally, is available at https://
www.epa.gov/dockets.
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II. Summary of Petitioned-For
Tolerance
In the Federal Register of July 5, 2023
(88 FR 42935) (FRL–10579–05–OCSPP)
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 3E9059) by Bayer
CropScience LP, 800 N Lindbergh Blvd.,
St. Louis, MO 63167. The petition
requested to establish a tolerance in 40
CFR part 180 for residues of the
insecticide, tetraniliprole [1-(3-chloro-2pyridinyl)-N-[4-cyano-2-methyl-6[(methylamino)carbonyl]phenyl]-3-[[5(trifluoromethyl)-2H-tetrazol-2yl]methyl]-1H-pyrazole-5-carboxamide],
in or on Tea, dried at 80 parts per
million (ppm). That document
referenced a summary of the petition,
which is available in the docket, https://
www.regulations.gov. Two comments
were received in response to the Notice
of Filing. EPA’s response to these
comments can be found in section IV.C.
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
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reasonable certainty that no harm will
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 tetraniliprole
including exposure resulting from the
tolerances established by this action.
EPA’s assessment of exposures and risks
associated with tetraniliprole 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 rulemaking of
the same pesticide chemical. Where
scientific information concerning a
particular chemical remains unchanged,
the content of those sections would not
vary between tolerance rulemaking, 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.
EPA has previously published a
tolerance rulemaking for tetraniliprole
in which EPA concluded, based on the
available information, that there is a
reasonable certainty that no harm would
result from aggregate exposure to
tetraniliprole and established tolerances
for residues of that chemical. EPA is
incorporating previously published
sections from this rulemaking as
described further in this rulemaking, as
they remain unchanged.
A. Toxicological Profile
For a discussion of the Toxicological
Profile of tetraniliprole, see Unit III.A. of
the tetraniliprole tolerance rulemaking
published in the Federal Register of
February 24, 2021 (86 FR 11133) (FRL–
10005–77).
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B. Toxicological Points of Departure/
Levels of Concern
Based on a thorough analysis of the
toxicology database of tetraniliprole, the
Agency has determined that a
qualitative risk assessment is more
appropriate for tetraniliprole than a
quantitative risk assessment. For more
details, please reference Unit III.B. of
the February 24, 2021, rulemaking.
C. Exposure Assessment
There is potential for exposure to
tetraniliprole via food and feed based on
the proposed tolerance for residues on
imported tea. However, no adverse
effects were observed in the submitted
toxicological studies for tetraniliprole
regardless of the route of exposure.
Thus, no quantitative dietary exposure
assessments are needed for EPA to
conclude with reasonable certainty that
dietary exposures to tetraniliprole do
not pose a significant human health
risk.
Drinking water and non-occupational
exposures. There are no residues of
toxicological concern expected in
drinking water from the use of
tetraniliprole. Thus, no drinking water
exposure assessments are needed for the
Agency to conclude with reasonable
certainty that drinking water exposures
to tetraniliprole do not pose a
significant human health risk.
Tetraniliprole is registered for use on
golf course turf and sports fields that
could result in residential postapplication exposures. However, no
adverse effects were observed in the
submitted toxicological studies for
tetraniliprole regardless of the route of
exposure; therefore, a quantitative
residential post-application exposure
assessment was not conducted. Thus, no
residential exposure assessments are
needed for the Agency to conclude with
reasonable certainty that residential
exposures to tetraniliprole do not pose
a significant human health risk.
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.’’
Unlike other pesticides for which EPA
has followed a cumulative risk approach
based on a common mechanism of
toxicity, EPA has not made a common
mechanism of toxicity finding as to
tetraniliprole and any other substances.
Tetraniliprole does not also appear to
produce a toxic metabolite produced by
other substances. For the purposes of
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Federal Register / Vol. 89, No. 95 / Wednesday, May 15, 2024 / Rules and Regulations
42389
this action, therefore, EPA has not
assumed that tetraniliprole has a
common mechanism of toxicity with
other substances.
Tolerance without U.S. Registration for
use on Tea. Summary of Analytical
Chemistry and Residue Data’’ in docket
ID EPA–HQ–OPP–2021–0624.
V. Conclusion
D. Safety Factor for Infants and
Children
Section 408(b)(2)(C) requires the
application of an additional tenfold
margin of safety to account for potential
risks to infants and children, in the case
of threshold effects. For tetraniliprole,
EPA has not identified any toxicological
endpoints of concern associated with
any threshold effects and is conducting
a qualitative assessment. That
qualitative assessment does not use
safety factors for assessing risk, and no
additional safety factor is needed for
assessing risk to infants and children.
EPA has also evaluated the available
data and concluded that there are no
residual uncertainties concerning the
potential risks to infants and children
that would impact its conclusions about
threshold effects.
IV. Other Considerations
VI. Statutory and Executive Order
Reviews
E. 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 populationadjusted dose (aPAD) and chronic
population-adjusted dose (cPAD). Short-,
intermediate-, and chronic-term risks
are evaluated by comparing the
estimated aggregate food, water, and
residential exposure to the appropriate
points of departure to ensure that an
adequate margin of exposure (MOE)
exists. For linear cancer risks, EPA
calculates the lifetime probability of
acquiring cancer given the estimated
aggregate exposure.
No adverse effects were observed in
the submitted toxicological studies at
doses relevant to human health
pesticide risk assessment for
tetraniliprole regardless of the route of
exposure. Effects observed in the data
base (e.g., decreased body weight) were
both marginal and only seen at doses
not expected to occur daily or over an
extended period.
Based on a lack of toxicity at exposure
levels expected from approved
application rates and an expectation
that aggregate exposures to residues of
tetraniliprole will not reach the levels
required to cause any adverse effects,
EPA concludes that there is a reasonable
certainty that no harm will result to the
general population, or to infants and
children from aggregate exposure to
tetraniliprole residues. More detailed
information on this action can be found
in the document titled ‘‘Tetraniliprole:
Petition for the Establishment of a
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15:57 May 14, 2024
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A. Analytical Enforcement Methodology
For a discussion of the available
analytical enforcement method, see Unit
IV.A. of the February 24, 2021,
rulemaking.
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).
There are no Codex MRLs for residues
of tetraniliprole in or on Tea, dried.
C. Response to Comments
Two comments were received in
response to the Notice of Filing from
different commenters. One commenter
stated in part that ‘‘I totally oppose
granting any tolerance changes or
added tolerances of any kind to any of
the toxic chemicals that are listed in
Federal Register notice’’. . . ‘‘none of
them should ever be approved or used
in the world. they are harmful . . .’’ The
other commenter opposed granting any
tolerances because all active ingredients
are harmful. This commenter also
mentioned results related to birth
defects from pesticides from a study but
did not provide a citation of said study.
Thus, the information cannot be
substantiated or addressed. According
to the commenter ‘‘Pesticide exposure
during susceptible windows and at
certain doses are linked to numerous
birth defects.’’ Holoprosencephaly
(HPE), malformation of the forebrain in
humans was the focus of this study,
according to the commenter. Although
the Agency recognizes that some
individuals believe that pesticides
should be banned, the existing legal
framework provided by section 408 of
the FFDCA authorizes EPA to establish
tolerances when it determines that the
tolerances are safe. Upon consideration
of the validity, completeness, and
reliability of the available data as well
as other factors the FFDCA requires EPA
to consider, EPA has determined that
the tetraniliprole tolerance on tea is
safe. The commenters have not provided
information indicating that a safety
determination cannot be supported.
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Therefore, tolerances are established
for residues of tetraniliprole in or on
Tea, dried at 80 ppm.
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 to
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).
Because tolerances and exemptions
that are established on the basis of a
petition under FFDCA section 408(d),
such as the tolerance 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
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Federal Register / Vol. 89, No. 95 / Wednesday, May 15, 2024 / Rules and Regulations
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).
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.
Dated: May 9, 2024.
Charles Smith,
Director, Registration Division, Office of
Pesticide Programs.
Therefore, for the reasons stated in the
preamble, EPA is amending 40 CFR
chapter 1 as follows:
PART 180—TOLERANCES AND
EXEMPTIONS FOR PESTICIDE
CHEMICAL RESIDUES IN FOOD
1. The authority citation for part 180
continues to read as follows:
■
Authority: 21 U.S.C. 321(q), 346a and 371.
2. In § 180.709, amend table 1 to
paragraph (a) by adding in alphabetical
order an entry ‘‘Tea, dried’’ to read as
follows:
■
§ 180.709 Tetraniliprole; tolerances for
residues.
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1 There is no U.S. Registration for this commodity as of May 15, 2024.
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[FR Doc. 2024–10559 Filed 5–14–24; 8:45 am]
BILLING CODE 6560–50–P
ENVIRONMENTAL PROTECTION
AGENCY
40 CFR Parts 281 and 282
[EPA–R08–UST–2023–0563; FRL–11550–
02–R8]
VII. Congressional Review Act
Commodity
Parts per
million
Commodity
80
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South Dakota: Final Approval of State
Underground Storage Tank Program
Revisions, Codification, and
Incorporation by Reference
Environmental Protection
Agency (EPA).
ACTION: Direct final rule.
AGENCY:
The State of South Dakota
Department of Agriculture and Natural
Resources (DANR) has applied to the
EPA for final approval of the changes to
its Underground Storage Tank (UST)
program under the Resource
Conservation and Recovery Act (RCRA).
The EPA has reviewed South Dakota’s
application and determined that South
Dakota’s UST program revisions satisfy
all requirements needed for program
approval. This action also codifies the
EPA’s approval of South Dakota’s State
program and incorporates by reference
those provisions of the State’s
regulations that we have determined
meet the requirements for approval.
DATES: This rule is effective on July 15,
2024 unless EPA receives adverse
written comment by June 14, 2024.
Should EPA receive such comments, it
will publish a timely document either:
withdrawing the direct final publication
or affirming the publication and
responding to comments. The
incorporation by reference of certain
publications listed in the regulations is
approved by the Director of the Federal
Register, as of July 15, 2024, in
accordance with 5 U.S.C. 552(a) and 1
CFR part 51.
ADDRESSES: Submit your comments by
one of the following methods:
Federal eRulemaking Portal: https://
www.regulations.gov. Follow the online
instructions for submitting comments.
Email: fitzgibbons.jeffrey@epa.gov.
Fax: (303) 312–6341 (prior to faxing,
please notify the EPA contact listed
below).
SUMMARY:
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Mail, hand delivery or courier: Jeff
Fitzgibbons, Resource Conservation and
Recovery Program, EPA Region 8,
Mailcode 8LCR–RC, 1595 Wynkoop
Street, Denver, Colorado 80202–1129.
Courier or hand deliveries are only
accepted during the Regional Office’s
normal hours of operation. The public is
advised to call in advance to verify
business hours. Special arrangements
should be made for deliveries of boxed
information.
Instructions: EPA must receive your
comments by June 14, 2024. Direct your
comments to Docket ID No. EPA–R08–
UST–2023–0563; FRL–11550–02–R8.
The EPA’s policy is that all comments
received will be included in the public
docket without change and may be
available online at https://
www.regulations.gov, including any
personal information provided, unless
the comment includes information
claimed to be Confidential Business
Information (CBI) or other information
whose disclosure is restricted by statute.
Do not submit information that you
consider to be CBI or otherwise
protected through https://
www.regulations.gov, or email. The
Federal https://www.regulations.gov
website is an ‘‘anonymous access’’
system, which means the EPA will not
know your identity or contact
information unless you provide it in the
body of your comment. If you send an
email comment directly to the EPA
without going through https://
www.regulations.gov, your email
address will be automatically captured
and included as part of the comment
that is placed in the public docket and
made available on the internet. If you
submit an electronic comment, the EPA
recommends that you include your
name and other contact information in
the body of your comment with any CD
you submit. If EPA cannot read your
comment due to technical difficulties
and cannot contact you for clarification,
EPA may not be able to consider your
comment. Electronic files should avoid
the use of special characters, any form
of encryption and be free of any defects
or viruses.
Docket: All documents in the docket
are listed in the https://
www.regulations.gov index. Although
listed in the index, some information is
not publicly available, e.g., CBI or other
information whose disclosure is
restricted by statute. Certain other
material, such as copyrighted material,
will be publicly available only in hard
copy. Publicly available docket
materials are available electronically
through https://www.regulations.gov.
For alternative access to docket
materials, please contact the person
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Agencies
[Federal Register Volume 89, Number 95 (Wednesday, May 15, 2024)]
[Rules and Regulations]
[Pages 42387-42390]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2024-10559]
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ENVIRONMENTAL PROTECTION AGENCY
40 CFR Part 180
[EPA-HQ-OPP-2021-0624; FRL-11958-01-OCSPP]
Tetraniliprole; Pesticide Tolerances
AGENCY: Environmental Protection Agency (EPA).
ACTION: Final rule.
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SUMMARY: This regulation establishes tolerance for residues of
tetraniliprole in or on tea, dried at 80 ppm. Bayer CropScience LP
requested this tolerance under the Federal Food, Drug, and Cosmetic Act
(FFDCA).
DATES: This regulation is effective May 15, 2024. Objections and
requests for hearings must be received on or before July 15, 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-2021-0624, 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 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-2021-0624 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
July 15, 2024. Addresses for mail and hand delivery of objections and
hearing requests are provided in 40 CFR 178.25(b).
EPA's Office of Administrative Law Judges (OALJ), in which the
Hearing Clerk is housed, urges parties to file and serve documents by
electronic means only, notwithstanding any other particular
requirements set forth in other procedural rules governing those
proceedings. See ``Revised Order Urging Electronic Service and
Filing'', dated June 22, 2023, which can be found at https://www.epa.gov/system/files/documents/2023-06/2023-06-22%20-%20revised%20order%20urging%20electronic%20filing%20and%20service.pdf.
Although EPA's regulations require submission via U.S. Mail or hand
delivery, EPA intends to treat submissions filed via electronic means
as properly filed submissions; therefore, EPA believes the preference
for submission via electronic means will not be prejudicial. When
submitting documents to the OALJ electronically, a person should
utilize the OALJ e-filing system at https://yosemite.epa.gov/oa/eab/eab-alj_upload.nsf.
In addition to filing an objection or hearing request with the
Hearing Clerk as described in 40 CFR part 178, please
[[Page 42388]]
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-2021-
0624, 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
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.
Additional instructions on commenting or visiting the docket, along
with more information about dockets generally, is available at https://www.epa.gov/dockets.
II. Summary of Petitioned-For Tolerance
In the Federal Register of July 5, 2023 (88 FR 42935) (FRL-10579-
05-OCSPP) 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
3E9059) by Bayer CropScience LP, 800 N Lindbergh Blvd., St. Louis, MO
63167. The petition requested to establish a tolerance in 40 CFR part
180 for residues of the insecticide, tetraniliprole [1-(3-chloro-2-
pyridinyl)-N-[4-cyano-2-methyl-6-[(methylamino)carbonyl]phenyl]-3-[[5-
(trifluoromethyl)-2H-tetrazol-2-yl]methyl]-1H-pyrazole-5-carboxamide],
in or on Tea, dried at 80 parts per million (ppm). That document
referenced a summary of the petition, which is available in the docket,
https://www.regulations.gov. Two comments were received in response to
the Notice of Filing. EPA's response to these comments can be found in
section IV.C.
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 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 tetraniliprole including exposure resulting from
the tolerances established by this action. EPA's assessment of
exposures and risks associated with tetraniliprole 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 rulemaking of the same pesticide
chemical. Where scientific information concerning a particular chemical
remains unchanged, the content of those sections would not vary between
tolerance rulemaking, 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.
EPA has previously published a tolerance rulemaking for
tetraniliprole in which EPA concluded, based on the available
information, that there is a reasonable certainty that no harm would
result from aggregate exposure to tetraniliprole and established
tolerances for residues of that chemical. EPA is incorporating
previously published sections from this rulemaking as described further
in this rulemaking, as they remain unchanged.
A. Toxicological Profile
For a discussion of the Toxicological Profile of tetraniliprole,
see Unit III.A. of the tetraniliprole tolerance rulemaking published in
the Federal Register of February 24, 2021 (86 FR 11133) (FRL-10005-77).
B. Toxicological Points of Departure/Levels of Concern
Based on a thorough analysis of the toxicology database of
tetraniliprole, the Agency has determined that a qualitative risk
assessment is more appropriate for tetraniliprole than a quantitative
risk assessment. For more details, please reference Unit III.B. of the
February 24, 2021, rulemaking.
C. Exposure Assessment
There is potential for exposure to tetraniliprole via food and feed
based on the proposed tolerance for residues on imported tea. However,
no adverse effects were observed in the submitted toxicological studies
for tetraniliprole regardless of the route of exposure. Thus, no
quantitative dietary exposure assessments are needed for EPA to
conclude with reasonable certainty that dietary exposures to
tetraniliprole do not pose a significant human health risk.
Drinking water and non-occupational exposures. There are no
residues of toxicological concern expected in drinking water from the
use of tetraniliprole. Thus, no drinking water exposure assessments are
needed for the Agency to conclude with reasonable certainty that
drinking water exposures to tetraniliprole do not pose a significant
human health risk.
Tetraniliprole is registered for use on golf course turf and sports
fields that could result in residential post-application exposures.
However, no adverse effects were observed in the submitted
toxicological studies for tetraniliprole regardless of the route of
exposure; therefore, a quantitative residential post-application
exposure assessment was not conducted. Thus, no residential exposure
assessments are needed for the Agency to conclude with reasonable
certainty that residential exposures to tetraniliprole do not pose a
significant human health risk.
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.'' Unlike other
pesticides for which EPA has followed a cumulative risk approach based
on a common mechanism of toxicity, EPA has not made a common mechanism
of toxicity finding as to tetraniliprole and any other substances.
Tetraniliprole does not also appear to produce a toxic metabolite
produced by other substances. For the purposes of
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this action, therefore, EPA has not assumed that tetraniliprole has a
common mechanism of toxicity with other substances.
D. Safety Factor for Infants and Children
Section 408(b)(2)(C) requires the application of an additional
tenfold margin of safety to account for potential risks to infants and
children, in the case of threshold effects. For tetraniliprole, EPA has
not identified any toxicological endpoints of concern associated with
any threshold effects and is conducting a qualitative assessment. That
qualitative assessment does not use safety factors for assessing risk,
and no additional safety factor is needed for assessing risk to infants
and children. EPA has also evaluated the available data and concluded
that there are no residual uncertainties concerning the potential risks
to infants and children that would impact its conclusions about
threshold effects.
E. 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). Short-, intermediate-, and chronic-term risks are
evaluated by comparing the estimated aggregate food, water, and
residential exposure to the appropriate points of departure to ensure
that an adequate margin of exposure (MOE) exists. For linear cancer
risks, EPA calculates the lifetime probability of acquiring cancer
given the estimated aggregate exposure.
No adverse effects were observed in the submitted toxicological
studies at doses relevant to human health pesticide risk assessment for
tetraniliprole regardless of the route of exposure. Effects observed in
the data base (e.g., decreased body weight) were both marginal and only
seen at doses not expected to occur daily or over an extended period.
Based on a lack of toxicity at exposure levels expected from
approved application rates and an expectation that aggregate exposures
to residues of tetraniliprole will not reach the levels required to
cause any adverse effects, EPA concludes that there is a reasonable
certainty that no harm will result to the general population, or to
infants and children from aggregate exposure to tetraniliprole
residues. More detailed information on this action can be found in the
document titled ``Tetraniliprole: Petition for the Establishment of a
Tolerance without U.S. Registration for use on Tea. Summary of
Analytical Chemistry and Residue Data'' in docket ID EPA-HQ-OPP-2021-
0624.
IV. Other Considerations
A. Analytical Enforcement Methodology
For a discussion of the available analytical enforcement method,
see Unit IV.A. of the February 24, 2021, rulemaking.
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).
There are no Codex MRLs for residues of tetraniliprole in or on
Tea, dried.
C. Response to Comments
Two comments were received in response to the Notice of Filing from
different commenters. One commenter stated in part that ``I totally
oppose granting any tolerance changes or added tolerances of any kind
to any of the toxic chemicals that are listed in Federal Register
notice''. . . ``none of them should ever be approved or used in the
world. they are harmful . . .'' The other commenter opposed granting
any tolerances because all active ingredients are harmful. This
commenter also mentioned results related to birth defects from
pesticides from a study but did not provide a citation of said study.
Thus, the information cannot be substantiated or addressed. According
to the commenter ``Pesticide exposure during susceptible windows and at
certain doses are linked to numerous birth defects.'' Holoprosencephaly
(HPE), malformation of the forebrain in humans was the focus of this
study, according to the commenter. Although the Agency recognizes that
some individuals believe that pesticides should be banned, the existing
legal framework provided by section 408 of the FFDCA authorizes EPA to
establish tolerances when it determines that the tolerances are safe.
Upon consideration of the validity, completeness, and reliability of
the available data as well as other factors the FFDCA requires EPA to
consider, EPA has determined that the tetraniliprole tolerance on tea
is safe. The commenters have not provided information indicating that a
safety determination cannot be supported.
V. Conclusion
Therefore, tolerances are established for residues of
tetraniliprole in or on Tea, dried at 80 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 to 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).
Because tolerances and exemptions that are established on the basis
of a petition under FFDCA section 408(d), such as the tolerance 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
[[Page 42390]]
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.
Dated: May 9, 2024.
Charles Smith,
Director, Registration Division, Office of Pesticide Programs.
Therefore, for the reasons stated in the preamble, EPA is amending
40 CFR chapter 1 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. 180.709, amend table 1 to paragraph (a) by adding in
alphabetical order an entry ``Tea, dried'' to read as follows:
Sec. 180.709 Tetraniliprole; tolerances for residues.
(a) * * *
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Parts per
Commodity million
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* * * * *
Tea, dried \1\.............................................. 80
* * * * *
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\1\ There is no U.S. Registration for this commodity as of May 15, 2024.
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[FR Doc. 2024-10559 Filed 5-14-24; 8:45 am]
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