Fluazinam; Pesticide Tolerances, 21946-21948 [2017-09590]
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21946
Federal Register / Vol. 82, No. 90 / Thursday, May 11, 2017 / Rules and Regulations
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Pepper/Eggplant, subgroup 8–
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Tea1 ............................................
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Tomato subgroup 8–10A ............
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(7505P), Office of Pesticide Programs,
Environmental Protection Agency, 1200
Pennsylvania Ave. NW., Washington,
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DC 20460–0001; main telephone
number: (703) 305–7090; email address:
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RDFRNotices@epa.gov.
SUPPLEMENTARY INFORMATION:
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[FR Doc. 2017–09592 Filed 5–10–17; 8:45 am]
BILLING CODE 6560–50–P
ENVIRONMENTAL PROTECTION
AGENCY
40 CFR Part 180
[EPA–HQ–OPP–2016–0160; FRL–9960–50]
Fluazinam; Pesticide Tolerances
Environmental Protection
Agency (EPA).
ACTION: Final rule.
AGENCY:
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14:36 May 10, 2017
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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
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?
This regulation establishes a
tolerance for residues of fluazinam in or
on tea, dried. ISK Biosciences
Corporation requested this tolerance
under the Federal Food, Drug, and
Cosmetic Act (FFDCA).
DATES: This regulation is effective May
11, 2017. Objections and requests for
hearings must be received on or before
July 10, 2017, 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–2016–0160, 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 is (202) 566–1744,
and the telephone number for the OPP
Docket is (703) 305–5805. Please review
the visitor instructions and additional
information about the docket available
at https://www.epa.gov/dockets.
FOR FURTHER INFORMATION CONTACT:
Michael Goodis, Registration Divison
SUMMARY:
I. General Information
You may access a frequently updated
electronic version of EPA’s tolerance
regulations at 40 CFR part 180 through
the Government Printing Office’s e-CFR
site at https://www.ecfr.gov/cgi-bin/textidx?&c=ecfr&tpl=/ecfrbrowse/Title40/
40tab_02.tpl.
C. How can I file an objection or hearing
request?
Under FFDCA section 408(g), 21
U.S.C. 346a, 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–2016–0160 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 10, 2017. 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
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Fmt 4700
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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–
2016–0160, 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/contacts.html.
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 May 19,
2016 (81 FR 31583) (FRL–9946–02),
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 6E8449) by ISK
Biosciences Corporation, 7470 Auburn
RD, Suite A, Concord, OH 44077. The
petition requested that 40 CFR 180.574
be amended by establishing tolerances
for residues of the fungicide fluazinam,
in or on dried tea at 5.0 parts per
million (ppm). That document
referenced a summary of the petition
prepared by ISK Biosciences
Corporation, the registrant, which is
available in the docket, https://
www.regulations.gov. One comment was
received on the notice of filing. EPA’s
response to these comments is
discussed in Unit IV.C.
Based upon review of the data
supporting the petition, EPA has revised
the proposed tolerance from 5.0 ppm to
6.0 ppm. The reason for these changes
are 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
result from aggregate exposure to the
pesticide chemical residue, including
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Federal Register / Vol. 82, No. 90 / Thursday, May 11, 2017 / Rules and Regulations
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 in
FFDCA section 408(b)(2)(D), 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 fluazinam
including exposure resulting from the
tolerances established by this action.
EPA’s assessment of exposures and risks
associated with fluazinam follows.
In the Federal Register of April 8,
2016 (81 FR 20545) (FRL 9942–99), EPA
established tolerances for residues of
fluazinam in or on cabbage at 3.0 parts
per million (ppm), mayhaw at 2.0 ppm,
the cucurbit vegetable crop group 9 at
0.07 ppm, and the tuberous and corm
vegetable subgroup 1C at 0.02 ppm, and
amended the commodity definition for
the existing tolerance in vegetable,
Brassica leafy, group 5 to vegetable,
Brassica leafy, group 5, except cabbage.
Fluazinam is also registered for use in
other plant commodities at levels
ranging from 0.01 ppm to 7.0 ppm. A
tolerance (without US registration) has
been established for residues of
fluazinam and its metabolite AMGT
in/on wine grapes at 3.0 ppm, and
tolerances of 0.05 ppm have been
established for residues of fluazinam
and its metabolites AMPA and DAPA
and their sulfamate conjugates in/on the
fat and meat byproducts of cattle, goats,
horses, and sheep.
ISK Biosciences submitted 5 field
trials for fluazinam on dried tea. The
Agency finds these data are acceptable
and sufficient to support the requested
tolerance. The Agency also determined
that establishing this tolerance would
not result in any change in the exposure
estimates from the previous risk
assessment for fluazinam. Since the
publication of the April 8, 2016 final
rule, the toxicity profile of fluazinam
has not changed, and the risk
assessments that supported the
establishment of those tolerances
published in the Federal Register
remain valid. The dietary risks for
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fluazinam are based on the parent
compound for bulb vegetables and in
root and tuber vegetables. For all other
plant commodities, the residues of
concern in plants for risk assessment are
fluazinam and its metabolite AMGT. In
drinking water, the degradates of
concern are parent fluazinam and its
transformation products. In livestock
commodities, the residues of concern
are fluazinam, the metabolites AMPA,
DAPA, and their sulfamate conjugates.
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 fluazinam residues.
For a detailed discussion of the
aggregate risk assessments and
determination of safety for the proposed
tolerances, please refer to the April 8,
2016 Federal Register document and its
supporting documents, available at
https://www.regulations.gov in docket ID
number EPA–HQ–OPP–2015–0197.
IV. Other Considerations
A. Analytical Enforcement Methodology
Adequate enforcement methodology
(a gas chromatographic method 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
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).
The 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 an
MRL for fluazinam in any commodities.
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C. Response to Comments
EPA received one comment to the
published Notice of Filing. This
comment stated, in part and without
any supporting information, that EPA
should deny this petition because it is
a harmful and toxic chemical with no
benefits. The Agency recognizes that
some individuals believe that pesticides
should be banned on agricultural crops.
The existing legal framework provided
by section 408 of the Federal Food,
Drug, and Cosmetic Act (FFDCA),
however, states that tolerances may be
set when persons seeking such
tolerances or exemptions have
demonstrated that the pesticide meets
the safety standard imposed by that
statute. EPA has assessed the effects of
this chemical on human health and
determined that aggregate exposure to it
will be safe. This comment provides no
information to support an alternative
conclusion.
D. Revisions to Petitioned-For
Tolerances
The petitioner proposed tolerances for
fluazinam in or on dried tea at 5.0 ppm.
When mean residues from each of the
tea field trials were entered into the
Organization for Economic Cooperation
and Development (OECD) MRL/
Tolerance Calculation Procedure, the
resulting tolerance was 6.0 ppm.
Therefore, EPA is establishing a
tolerance of 6.0 ppm rather than the
requested tolerance of 5.0 ppm.
V. Conclusion
Therefore, a tolerance is established
for residues of fluazinam, 3-chloro-N-[3chloro-2,6-dinitro-4(trifluoromethyl)phenyl]-5(trifluoromethyl)-2-pyridinamine, in or
on tea, dried at 6.0 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
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Federal Register / Vol. 82, No. 90 / Thursday, May 11, 2017 / Rules and Regulations
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 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 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).
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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).
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14:36 May 10, 2017
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List of Subjects in 40 CFR Part 180
Environmental protection,
Administrative practice and procedure,
Agricultural commodities, Pesticides
and pests, Reporting and recordkeeping
requirements.
Dated: March 28, 2017.
Michael Goodis,
Director, Registration Division, Office of
Pesticide Programs.
Therefore, 40 CFR chapter I is
amended as follows:
■
PART 180—[AMENDED]
1. The authority citation for part 180
continues to read as follows:
■
Authority: 21 U.S.C. 321(q), 346a and 371.
2. In § 180.574, add alphabetically the
entry ‘‘Tea, dried 1’’ and footnote 1 to
the table in paragraph (a)(1) to read as
follows:
■
§ 180.574 Fluazinam; tolerances for
residues.
(a) * * *
(1) * * *
This final rule announces
inseason changes to management
measures in the Pacific Coast groundfish
fishery. This action implements an
increase in the incidental Pacific halibut
retention ratio in the sablefish primary
fishery, and changes to recreational
fisheries management measures that
will reduce recreational groundfish and
rockfish bag limits and eliminate length
requirements for recreationally caught
lingcod in all areas.
DATES: This final rule is effective May
11, 2017.
FOR FURTHER INFORMATION CONTACT:
Benjamin Mann phone: 206–526–6117,
fax: 206–526–6736, or email:
Benjamin.mann@noaa.gov.
SUMMARY:
SUPPLEMENTARY INFORMATION:
Electronic Access
This rule is accessible via the Internet
at the Office of the Federal Register Web
site at https://www.federalregister.gov.
Background information and documents
are available at the Pacific Fishery
Management Council’s Web site at
https://www.pcouncil.org/.
Parts per
million
Background
The Pacific Fishery Management
Council (Council)—in coordination with
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the International Pacific Halibut
Tea, dried 1 .................................
6.0 Commission (IPHC) and the States of
Washington, Oregon, and California—
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recommended changes to groundfish
1 There is no U.S. registration as of January
management measures at its March 7–
19, 2017.
13, 2017, meeting. Specifically, the
Council recommended (1) an increase in
*
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incidental halibut retention allocation
[FR Doc. 2017–09590 Filed 5–10–17; 8:45 am]
in the primary sablefish fishery from
BILLING CODE 6560–50–P
110 lbs dressed weight halibut per 1,000
lbs dressed weight sablefish, to 140 lbs
halibut to 1,000 lbs sablefish to improve
DEPARTMENT OF COMMERCE
opportunity for industry to harvest more
of the sablefish allocation without
National Oceanic and Atmospheric
exceeding it or the incidental halibut
Administration
allocation ACLs, and (2) a reduction in
rockfish bag limits in the Washington
50 CFR Part 660
recreational groundfish fishery (all
areas) from 10 to 7 rockfish per angler,
[Docket No. 160808696–7010–02]
a reduction in the aggregated groundfish
RIN 0648–BG76
daily bag limit from 12 to 9 fish per
angler, and finally, removal of the 22Magnuson-Stevens Act Provisions;
inch minimum size limit for lingcod
Fisheries Off West Coast States;
retention.
Pacific Coast Groundfish Fishery;
2017–2018 Biennial Specifications and Increased Incidental Halibut Retention
Management Measures; Inseason
in the Limited Entry Fixed Gear
Adjustments
Sablefish Primary Fishery
The IPHC establishes total allowable
AGENCY: National Marine Fisheries
catch (TAC) amounts for Pacific halibut
Service (NMFS), National Oceanic and
each year in January. Under the
Atmospheric Administration (NOAA),
authority of the Northern Pacific Halibut
Commerce.
Act, and implementing regulations at 50
ACTION: Final rule; inseason adjustments
CFR 300.63, a Catch Sharing Plan for
to biennial groundfish management
IPHC Area 2A (waters off the U.S. West
measures.
Coast), developed by the Council and
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Agencies
[Federal Register Volume 82, Number 90 (Thursday, May 11, 2017)]
[Rules and Regulations]
[Pages 21946-21948]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2017-09590]
-----------------------------------------------------------------------
ENVIRONMENTAL PROTECTION AGENCY
40 CFR Part 180
[EPA-HQ-OPP-2016-0160; FRL-9960-50]
Fluazinam; Pesticide Tolerances
AGENCY: Environmental Protection Agency (EPA).
ACTION: Final rule.
-----------------------------------------------------------------------
SUMMARY: This regulation establishes a tolerance for residues of
fluazinam in or on tea, dried. ISK Biosciences Corporation requested
this tolerance under the Federal Food, Drug, and Cosmetic Act (FFDCA).
DATES: This regulation is effective May 11, 2017. Objections and
requests for hearings must be received on or before July 10, 2017, 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-2016-0160, 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 is (202) 566-1744, and the telephone number for the OPP
Docket is (703) 305-5805. Please review the visitor instructions and
additional information about the docket available at https://www.epa.gov/dockets.
FOR FURTHER INFORMATION CONTACT: Michael Goodis, Registration Divison
(7505P), Office of Pesticide Programs, Environmental Protection Agency,
1200 Pennsylvania Ave. NW., Washington, DC 20460-0001; main telephone
number: (703) 305-7090; email address: RDFRNotices@epa.gov.
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 Government
Printing Office's e-CFR site at https://www.ecfr.gov/cgi-bin/text-idx?&c=ecfr&tpl=/ecfrbrowse/Title40/40tab_02.tpl.
C. How can I file an objection or hearing request?
Under FFDCA section 408(g), 21 U.S.C. 346a, 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-2016-0160 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 10, 2017. 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-2016-0160, 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/contacts.html.
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 May 19, 2016 (81 FR 31583) (FRL-9946-
02), 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
6E8449) by ISK Biosciences Corporation, 7470 Auburn RD, Suite A,
Concord, OH 44077. The petition requested that 40 CFR 180.574 be
amended by establishing tolerances for residues of the fungicide
fluazinam, in or on dried tea at 5.0 parts per million (ppm). That
document referenced a summary of the petition prepared by ISK
Biosciences Corporation, the registrant, which is available in the
docket, https://www.regulations.gov. One comment was received on the
notice of filing. EPA's response to these comments is discussed in Unit
IV.C.
Based upon review of the data supporting the petition, EPA has
revised the proposed tolerance from 5.0 ppm to 6.0 ppm. The reason for
these changes are 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 result from aggregate exposure
to the pesticide chemical residue, including
[[Page 21947]]
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 in FFDCA section 408(b)(2)(D), 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 fluazinam including exposure
resulting from the tolerances established by this action. EPA's
assessment of exposures and risks associated with fluazinam follows.
In the Federal Register of April 8, 2016 (81 FR 20545) (FRL 9942-
99), EPA established tolerances for residues of fluazinam in or on
cabbage at 3.0 parts per million (ppm), mayhaw at 2.0 ppm, the cucurbit
vegetable crop group 9 at 0.07 ppm, and the tuberous and corm vegetable
subgroup 1C at 0.02 ppm, and amended the commodity definition for the
existing tolerance in vegetable, Brassica leafy, group 5 to vegetable,
Brassica leafy, group 5, except cabbage. Fluazinam is also registered
for use in other plant commodities at levels ranging from 0.01 ppm to
7.0 ppm. A tolerance (without US registration) has been established for
residues of fluazinam and its metabolite AMGT in/on wine grapes at 3.0
ppm, and tolerances of 0.05 ppm have been established for residues of
fluazinam and its metabolites AMPA and DAPA and their sulfamate
conjugates in/on the fat and meat byproducts of cattle, goats, horses,
and sheep.
ISK Biosciences submitted 5 field trials for fluazinam on dried
tea. The Agency finds these data are acceptable and sufficient to
support the requested tolerance. The Agency also determined that
establishing this tolerance would not result in any change in the
exposure estimates from the previous risk assessment for fluazinam.
Since the publication of the April 8, 2016 final rule, the toxicity
profile of fluazinam has not changed, and the risk assessments that
supported the establishment of those tolerances published in the
Federal Register remain valid. The dietary risks for fluazinam are
based on the parent compound for bulb vegetables and in root and tuber
vegetables. For all other plant commodities, the residues of concern in
plants for risk assessment are fluazinam and its metabolite AMGT. In
drinking water, the degradates of concern are parent fluazinam and its
transformation products. In livestock commodities, the residues of
concern are fluazinam, the metabolites AMPA, DAPA, and their sulfamate
conjugates.
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 fluazinam residues.
For a detailed discussion of the aggregate risk assessments and
determination of safety for the proposed tolerances, please refer to
the April 8, 2016 Federal Register document and its supporting
documents, available at https://www.regulations.gov in docket ID number
EPA-HQ-OPP-2015-0197.
IV. Other Considerations
A. Analytical Enforcement Methodology
Adequate enforcement methodology (a gas chromatographic method 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 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). The 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 an MRL for fluazinam in any
commodities.
C. Response to Comments
EPA received one comment to the published Notice of Filing. This
comment stated, in part and without any supporting information, that
EPA should deny this petition because it is a harmful and toxic
chemical with no benefits. The Agency recognizes that some individuals
believe that pesticides should be banned on agricultural crops. The
existing legal framework provided by section 408 of the Federal Food,
Drug, and Cosmetic Act (FFDCA), however, states that tolerances may be
set when persons seeking such tolerances or exemptions have
demonstrated that the pesticide meets the safety standard imposed by
that statute. EPA has assessed the effects of this chemical on human
health and determined that aggregate exposure to it will be safe. This
comment provides no information to support an alternative conclusion.
D. Revisions to Petitioned-For Tolerances
The petitioner proposed tolerances for fluazinam in or on dried tea
at 5.0 ppm. When mean residues from each of the tea field trials were
entered into the Organization for Economic Cooperation and Development
(OECD) MRL/Tolerance Calculation Procedure, the resulting tolerance was
6.0 ppm. Therefore, EPA is establishing a tolerance of 6.0 ppm rather
than the requested tolerance of 5.0 ppm.
V. Conclusion
Therefore, a tolerance is established for residues of fluazinam, 3-
chloro-N-[3-chloro-2,6-dinitro-4-(trifluoromethyl)phenyl]-5-
(trifluoromethyl)-2-pyridinamine, in or on tea, dried at 6.0 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
[[Page 21948]]
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 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 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: March 28, 2017.
Michael Goodis,
Director, Registration Division, Office of Pesticide Programs.
0
Therefore, 40 CFR chapter I is amended as follows:
PART 180--[AMENDED]
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. 180.574, add alphabetically the entry ``Tea, dried \1\''
and footnote 1 to the table in paragraph (a)(1) to read as follows:
Sec. 180.574 Fluazinam; tolerances for residues.
(a) * * *
(1) * * *
------------------------------------------------------------------------
Parts per
Commodity million
------------------------------------------------------------------------
* * * * *
Tea, dried \1\.............................................. 6.0
* * * * *
------------------------------------------------------------------------
\1\ There is no U.S. registration as of January 19, 2017.
* * * * *
[FR Doc. 2017-09590 Filed 5-10-17; 8:45 am]
BILLING CODE 6560-50-P