Methoxyfenozide; Pesticide Tolerances and Time-Limited Pesticide Tolerances, 11820-11826 [E8-4027]
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Federal Register / Vol. 73, No. 44 / Wednesday, March 5, 2008 / Rules and Regulations
(MRLs) for cloquintocet-mexyl on wheat
and barley at 0.1 ppm.
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F. Determination of Safety and
Conclusions
The Agency is granting the requested
increase in tolerances for cloquintocetmexyl and its metabolite on wheat,
forage at 0.20 ppm and wheat, hay at
0.50 ppm. The Agency is also granting
the requested addition of reference to
the active ingredient pyroxsulam for use
with the inert ingredient safener
cloquintocet-mexyl on wheat. In
addition, the Agency is removing the
specification of a 1:4 ratio of
cloquintocet-mexyl to active ingredient
from the existing tolerance expression of
40 CFR 180.560. The specification is not
necessary when numerical tolerances
are already established.
Based on the information in this
preamble, EPA concludes that there is a
reasonable certainty of no harm to the
general population, including infants
and children, from aggregate exposure
to residues of cloquintocet-mexyl and
its metabolite. Accordingly, EPA finds
that the tolerances described above for
residues of cloquintocet-mexyl and its
metabolite will be safe.
IV. Statutory and Executive Order
Reviews
This final rule establishes a tolerance
under section 408(d) of FFDCA in
response to petitions 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 rule has
been exempted from review under
Executive Order 12866, this rule is not
subject to Executive Order 13211,
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 final rule 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 section 408(d) of FFDCA, such as
the tolerance in this final rule, do not
require the issuance of a proposed rule,
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the requirements of the Regulatory
Flexibility Act (RFA) (5 U.S.C. 601 et
seq.) do not apply.
This final rule 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 section 408(n)(4) of FFDCA. 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 6, 2000) do not apply
to this rule. In addition, this rule does
not impose any enforceable duty or
contain any unfunded mandate as
described under Title II of the Unfunded
Mandates Reform Act of 1995 (UMRA)
(Public Law 104–4).
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 of 1995
(NTTAA), Public Law 104–113, section
12(d) (15 U.S.C. 272 note).
V. Congressional Review Act
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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Therefore, 40 CFR chapter I is
amended as follows:
I
PART 180—[AMENDED]
1. The authority citation for part 180
continues to read as follows:
I
Authority: 21 U.S.C. 321(q), 346a and 371.
2. Section 180.560 is amended by
revising paragraph (a) to read as follows:
I
§ 180.560 Cloquintocet-mexyl (acetic acid
[(5-chloro-8-quinolinyl) oxy]-, 1-methylhexyl
ester; CAS Reg. No. 99607–70–2);
tolerances for residues.
(a) General. Tolerances are
established for the combined residues of
cloquintocet-mexyl (acetic acid [(5chloro-8-quinolinyl) oxy]-, 1methylhexyl ester; CAS Reg. No. 99607–
70–2) and its acid metabolite (5-chloro8-quinlinoxyacetic acid) when used as
an inert ingredient (safener) in pesticide
formulations containing the active
ingredients pinoxaden (wheat or barley),
clodinafop-propargyl (wheat only), or
pyroxsulum (wheat only) in or on the
following food commodities:
Commodity
Parts per million
Barley, grain ............
Barley, hay ..............
Barley, straw ...........
Wheat, forage ..........
Wheat, grain ............
Wheat, hay ..............
Wheat, straw ...........
*
*
*
*
0.1
0.1
0.1
0.2
0.1
0.5
0.1
*
[FR Doc. E8–4023 Filed 3–4–08; 8:45 am]
The Congressional Review Act, 5
U.S.C. 801 et seq., generally provides
that before a rule may take effect, the
agency promulgating the rule must
submit a rule report to each House of
the Congress and to the Comptroller
General of the United States. 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 this final rule in the
Federal Register. This final rule is not
a ‘‘major rule’’ as defined by 5 U.S.C.
804(2).
PO 00000
Dated: February 20, 2008.
Lois Rossi,
Director, Registration Division, Office of
Pesticide Programs.
BILLING CODE 6560–50–S
ENVIRONMENTAL PROTECTION
AGENCY
40 CFR Part 180
[EPA–HQ–OPP–2007–0495; FRL–8352–2]
Methoxyfenozide; Pesticide Tolerances
and Time-Limited Pesticide Tolerances
Environmental Protection
Agency (EPA).
ACTION: Final rule.
AGENCY:
SUMMARY: This regulation establishes
tolerances for residues of
methoxyfenozide per se; benzoic acid,
3-methoxy-2-methyl-2-(3,5dimethylbenzoyl)-2-(1,1dimethylethyl)hydrazide in or on the
food commodities acerola; animal feed,
nongrass, group 18, forage; animal feed,
nongrass, group 18, hay; avocado; bean,
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Federal Register / Vol. 73, No. 44 / Wednesday, March 5, 2008 / Rules and Regulations
dry, seed; bushberry subgroup 13-07B;
canistel; feijoa; grass, forage, fodder and
hay, group 17, forage; grass, forage,
fodder and hay, group 17, hay; guava;
jaboticaba; kurrat; mango; onion, green,
subgroup 3-07B; papaya; passionfruit;
peanut; peanut, hay; peanut oil;
sapodilla; sapote, black; sapote, mamey;
star apple; starfruit; vegetable, tuberous
and corm, except potato, sub group 1D;
and wax jambu. This regulation also
establishes time-limited tolerances for
indirect or inadvertent residues of
methoxyfenozide; benzoic acid, 3methoxy-2-methyl-, 2-(3,5dimethylbenzoyl)-2-(1,1-dimethylethyl)
hydrazide and indirect or inadvertent
combined residues of methoxyfenozide
and its metabolites RH-117,236 free
phenol of methoxyfenozide; 3,5dimethylbenzoic acid N-tert-butyl-N’-(3hydroxy-2-methylbenzoyl) hydrazide,
RH-151,055 glucose conjugate of RH117,236; 3,5-dimethyl benzoic acid Ntert-butyl-N-[3 ([beta]-Dglucopyranosyloxy)-2-methylbenzoyl]hydrazide and RH-152,072 the
malonylglycosyl conjugate of RH
117,236 in or on the food commodities
animal feed, nongrass, group 18; grain,
cereal, forage, fodder and straw, group
16; grass forage, fodder, and hay, group
17; herb and spice, group 19; vegetable,
bulb, group 3-07; vegetable, foliage of
legume, group 7; vegetable, leaves of
root and tuber, group 2; vegetable,
legume, group 6; and vegetable, root and
tuber, group 1. Dow AgroSciences LLC
and Interregional Research Project
Number 4 (IR-4) requested these
tolerances under the Federal Food,
Drug, and Cosmetic Act (FFDCA). The
time-limited tolerances will expire on
September 30, 2010.
DATES: This regulation is effective
March 5, 2008. Objections and requests
for hearings must be received on or
before May 5, 2008, 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: EPA has established a
docket for this action under docket
identification (ID) number EPA–HQ–
OPP–2007–0495. To access the
electronic docket, go to https://
www.regulations.gov, select ‘‘Advanced
Search,’’ then ‘‘Docket Search.’’ Insert
the docket ID number where indicated
and select the ‘‘Submit’’ button. Follow
the instructions on the regulations.gov
website to view the docket index or
access available documents. All
documents in the docket are listed in
the docket index available in
regulations.gov. Although listed in the
index, some information is not publicly
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available, e.g., Confidential Business
Information (CBI) or other information
whose disclosure is restricted by statute.
Certain other material, such as
copyrighted material, is not placed on
the Internet and will be publicly
available only in hard copy form.
Publicly available docket materials are
available either in the electronic docket
at https://www.regulations.gov, or, if only
available in hard copy, at the OPP
Public Docket, in Rm. S–4400, One
Potomac Yard (South Bldg.), 2777 S.
Crystal Dr., Arlington, VA. The Docket
Facility is open from 8:30 a.m. to 4 p.m.,
Monday through Friday, excluding legal
holidays. The Docket Facility telephone
number is (703) 305–5805.
FOR FURTHER INFORMATION CONTACT:
Mark Suarez, Registration Division
(7505P), Office of Pesticide Programs,
Environmental Protection Agency, 1200
Pennsylvania Ave., NW., Washington,
DC 20460–0001; telephone number:
(703) 305–0120; e-mail address:
suarez.mark@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. Potentially
affected entities may include, but are
not limited to those engaged in the
following activities:
• Crop production (NAICS code 111),
e.g., agricultural workers; greenhouse,
nursery, and floriculture workers;
farmers.
• Animal production (NAICS code
112), e.g., cattle ranchers and farmers,
dairy cattle farmers, livestock farmers.
• Food manufacturing (NAICS code
311) , e.g., agricultural workers; farmers;
greenhouse, nursery, and floriculture
workers; ranchers; pesticide applicators.
• Pesticide manufacturing (NAICS
code 32532), e.g., agricultural workers;
commercial applicators; farmers;
greenhouse, nursery, and floriculture
workers; residential users.
This listing is not intended to be
exhaustive, but rather provides a guide
for readers regarding entities likely to be
affected by this action. Other types of
entities not listed in this unit could also
be affected. The North American
Industrial Classification System
(NAICS) codes have been provided to
assist you and others in determining
whether this action might apply to
certain entities. If you have any
questions regarding the applicability of
this action to a particular entity, consult
the person listed under FOR FURTHER
INFORMATION CONTACT.
PO 00000
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B. How Can I Access Electronic Copies
of this Document?
In addition to accessing an electronic
copy of this Federal Register document
through the electronic docket at https://
www.regulations.gov, you may access
this Federal Register document
electronically through the EPA Internet
under the ‘‘Federal Register’’ listings at
https://www.epa.gov/fedrgstr. You may
also access a frequently updated
electronic version of 40 CFR part 180
through the Government Printing
Office’s pilot e-CFR site at https://
www.gpoaccess.gov/ecfr.
C. Can I File an Objection or Hearing
Request?
Under section 408(g) of FFDCA, as
amended by FQPA, any person may file
an objection to any aspect of this
regulation and may also request a
hearing on those objections. The EPA
procedural regulations which govern the
submission of objections and requests
for hearings appear in 40 CFR part 178.
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–2007–0495 in the subject line on
the first page of your submission. All
requests must be in writing, and must be
mailed or delivered to the Hearing Clerk
on or before May 5, 2008.
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 that does not
contain any CBI for inclusion in the
public docket that is described in
ADDRESSES. Information not marked
confidential pursuant to 40 CFR part 2
may be disclosed publicly by EPA
without prior notice. Submit your
copies, identified by docket ID number
EPA–HQ–OPP–2007–0495, by one of
the following methods:
• Federal eRulemaking Portal: https://
www.regulations.gov. Follow the on-line
instructions for submitting comments.
• Mail: Office of Pesticide Programs
(OPP) Regulatory Public Docket (7502P),
Environmental Protection Agency, 1200
Pennsylvania Ave., NW., Washington,
DC 20460–0001.
• Delivery: OPP Regulatory Public
Docket (7502P), Environmental
Protection Agency, Rm. S–4400, One
Potomac Yard (South Bldg., 2777 S.
Crystal Dr., Arlington, VA. Deliveries
are only accepted during the Docket’s
normal hours of operation (8:30 a.m. to
4 p.m., Monday through Friday,
excluding legal holidays). Special
arrangements should be made for
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deliveries of boxed information. The
Docket Facility telephone number is
(703) 305–5805.
II. Petition for Tolerances
In the Federal Register of October 20,
2006 (71 FR 61971) (FRL–8098–6),
August 1, 2007 (72 FR 42072) (FRL–
8138–1), and October 24, 2007 (72 FR
60367) (FRL–8154–1), EPA issued
notices pursuant to section 408(d)(3) of
FFDCA, 21 U.S.C. 346a(d)(3),
announcing the filing of pesticide
petitions (PPs 6E7086, 7E7218, 6F7135,
and 0F6201) by, Dow AgroSciences
LLC, Zionsville Road -Indianapolis, IN
46268 (PPs 6F7135 and 0F6201) and IR4, 500 College Road East, Suite 201 W.,
Princeton, NJ 08540 (PPs 7E7218 and
6E7086). The petitions requested that 40
CFR 180.544 be amended by
establishing tolerances for residues of
the insecticide, methoxyfenozide, in or
on the food commodities acerola at 0.4
parts per million (ppm) (PP 7E7218);
arionia berry at 3.0 ppm (PP 6E7086);
avocado at 0.6 ppm (PP 7E7218); bean,
dry, seed at 0.15 ppm (PP 6E7086);
blueberry, lowbush at 3.0 ppm (PP
6E7086); buffalo currant at 3.0 ppm (PP
6E7086); bushberry subgroup 13B at 3.0
ppm (PP 6E7086); canistel at 0.6 ppm
(PP 7E7218); Chilean guava at 3.0 ppm
(PP 6E7086); chive, Chinese, fresh
leaves at 5.0 ppm (PP 7E7218); chive,
fresh leaves at 5.0 ppm (PP 7E7218);
elegans hosta at 5.0 ppm (PP 7E7218);
European barberry at 3.0 ppm (PP
6E7086); feijoa at 0.4 ppm (PP 7E7218);
fritillaria leaves at 5.0 ppm (PP 7E7218);
grass forage, fodder, and hay group 17,
forage at 18.0 ppm (PP 6E7086); grass
forage, fodder, and hay, group 17, hay
at 30.0 ppm (PP 6E7086); guava at 0.4
ppm (PP 7E7218); highbush cranberry at
3.0 ppm (PP 6E7086); honeysuckle at
3.0 ppm (PP 6E7086); jaboticaba at 0.4
ppm (PP 7E7218); jostaberry at 3.0 ppm
(PP 6E7086); juneberry at 3.0 ppm (PP
6E7086); kurrat at 5.0 ppm (PP 7E7218);
Lady’s leek at 5.0 ppm (PP 7E7218); leek
at 5.0 ppm (PP 7E7218); leek, wild at 5.0
ppm (PP 7E7218); lingonberry at 3.0
ppm (PP 6E7086); mango at 0.6 ppm (PP
7E7218); native currant at 3.0 ppm (PP
6E7086); nongrass animal feeds, group
18, forage at 35.0 ppm (PP 6F7135);
nongrass animal feeds, group 18, hay at
85.0 ppm (PP 6F7135); onion, Beltsville
bunching at 5.0 ppm (PP 7E7218);
onion, fresh at 5.0 ppm (PP 7E7218);
onion, green at 5.0 ppm (PP 7E7218);
onion, macrostem at 5.0 ppm (PP
7E7218); onion, tree, tops at 5.0 ppm
(PP 7E7218); onion, Welsh, tops at 5.0
ppm (PP 7E7218); papaya at 0.6 ppm
(PP 7E7218); passionfruit at 0.4 ppm (PP
7E7218); peanut at 0.02 ppm (PP
6E7086); peanut, hay at 60 ppm (PP
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6E7086); peanut oil at 0.09 ppm (PP
6E7086); salal at 3.0 ppm (PP 6E7086);
sapodilla at 0.6 ppm (PP 7E7218);
sapote, black at 0.6 ppm (PP 7E7218);
sapote, mamey at 0.6 ppm (PP 7E7218);
sea buckthorn at 3.0 ppm (PP 6E7086);
shallot, fresh leaves at 5.0 ppm (PP
7E7218); star apple at 0.6 ppm (PP
7E7218); starfruit at 0.4 ppm (PP
7E7218); vegetable, tuberous and corm,
except potato, sub group 1D at 0.02 ppm
(PP 6E7086); wax jambu at 0.4 ppm (PP
7E7218). In the petition 0F6201, Dow
requested that tolerances that expired
on September 30, 2007 be re-established
for indirect or inadvertent residues of
methoxyfenozide; benzoic acid, 3methoxy-2-methyl-, 2-(3,5dimethylbenzoyl)-2-(1,1-dimethylethyl)
hydrazide and indirect or inadvertent
combined residues of methoxyfenozide;
benzoic acid, 3-methoxy-2-methyl-, 2(3,5-dimethylbenzoyl)-2-(1,1dimethylethyl) hydrazide and its
metabolites RH-117,236 free phenol of
methoxyfenozide; 3,5-dimethylbenzoic
acid N-tert-butyl-N’-(3-hydroxy-2methylbenzoyl) hydrazide, RH-151,055
glucose conjugate of RH-117,236; 3,5dimethyl benzoic acid N-tert-butyl-N-[3
([beta]-D-glucopyranosyloxy)-2methylbenzoyl]-hydrazide and RH152,072 the malonylglycosyl conjugate
of RH 117,236 in or on the food
commodities grain, cereal, forage,
fodder, and straw, group 16 at 10.0 ppm;
grass forage, fodder, and hay, group 17
at 10.0 ppm; herb and spice, group 19
at 10.0 ppm; nongrass animal feeds crop
group 18 at 10.0 ppm; vegetable, bulb,
group 3 at 0.2 ppm; vegetable, foliage of
legume, group 7 at 10.0 ppm; vegetable,
leaves of root and tuber, group 2 at 0.2
ppm; vegetable, legume, group 6 at 0.1
ppm; and vegetable, root and tuber,
group 1 at 0.1 ppm. Those notices
referenced summaries of the petitions
prepared by Dow AgroSciences LLC and
IR-4, the registrants, which are available
to the public in the docket, https://
www.regulations.gov. Comments were
received on the notices of filing. EPA’s
response to these comments is
discussed in Unit IV.C. The time-limited
tolerances will expire on September 30,
2010.
Based upon review of the data
supporting the petition, EPA has
modified the tolerance expression for
the food commodities bean, dry, seed to
0.24 ppm (PP 6E7086); animal feeds,
nongrass, group 18, forage to 50.0 ppm
(PP 6F7135); animal feeds, nongrass,
group 18, hay to 150.0 ppm (PP
6F7135); onions, green, subgroup 3-07B
at 5.0 ppm (PP 7E7218); peanut, hay to
55 ppm (PP 6E7086); peanut oil to 0.04
ppm (PP 6E7086). The reason for these
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changes is explained in Unit IV.D. EPA
is also deleting all the tolerances in
§ 180.544(b) for sorghum and soybean
commodities that are no longer needed
since they have expired. The deletions
under § 180.544(b) are time-limited
tolerances that were established under
section 18 emergency exemptions that
have since expired.
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. . . .’’
EPA performs a number of analyses to
determine the risks from aggregate
exposure to pesticide residues. For
further discussion of the regulatory
requirements of section 408 of FFDCA
and a complete description of the risk
assessment process, see https://
www.epa.gov/fedrgstr/EPA-PEST/1997/
November/Day-26/p30948.htm.
Consistent with section 408(b)(2)(D)
of FFDCA, 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,
consistent with section 408(b)(2) of
FFDCA, for tolerances for the
petitioned-for tolerances for residues of
methoxyfenozide on the food
commodities named above. EPA’s
assessment of exposures and risks
associated with establishing the
tolerance follows.
A. Toxicological Profile
EPA has evaluated the available
toxicity data and considered its validity,
completeness, and reliability as well as
the relationship of the results of the
studies to human risk. EPA has also
considered available information
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concerning the variability of the
sensitivities of major identifiable
subgroups of consumers, including
infants and children.
The toxicology studies conducted
with methoxyfenozide demonstrate that
it has few or no biologically significant
toxic effects at relatively low-dose levels
and only mild or no toxic effects at
relatively high-dose levels. In
subchronic and chronic oral studies in
rats, the most toxicologically significant
effects were mild anemia and mild
effects on the liver, thyroid gland, and
adrenal gland. In subchronic and
chronic oral studies in dogs, the
predominant toxic effect was anemia,
which was often accompanied by signs
of a compensatory response.
Methoxyfenozide is not acutely toxic,
not a dermal sensitizer, not neurotoxic,
carcinogenic or mutagenic and is not a
developmental or reproductive toxicant.
There was no evidence for increased
susceptibility of rat or rabbit fetuses to
in utero exposure or rat pups to postnatal exposure to methoxyfenozide.
Minimal or no toxic effects were
observed in studies in which
methoxyfenozide was administered by
the dermal or inhalation routes of
exposure. Methoxyfenozide is classified
as a ‘‘not likely’’ human carcinogen.
Specific information on the studies
received and the nature of the adverse
effects caused by methoxyfenozide as
well as the no-observed-adverse-effectlevel (NOAEL) and the lowest-observedadverse-effect-level (LOAEL) from the
toxicity studies can be found at https://
www.regulations.gov. The referenced
document is available in the docket
established by this action, which is
described under ADDRESSES, and is
identified as EPA–HQ–OPP–2007–0495
in that docket.
B. Toxicological Endpoints
For hazards that have a threshold
below which there is no appreciable
risk, the toxicological level of concern
(LOC) is derived from the highest dose
at which no adverse effects are observed
(the NOAEL) in the toxicology study
identified as appropriate for use in risk
assessment. However, if a NOAEL
cannot be determined, the lowest dose
at which adverse effects of concern are
identified (the LOAEL) is sometimes
used for risk assessment. Uncertainty/
safety factors (UFs) are used in
conjunction with the LOC to take into
account uncertainties inherent in the
extrapolation from laboratory animal
data to humans and in the variations in
sensitivity among members of the
human population as well as other
unknowns. Safety is assessed for acute
and chronic risks by comparing
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aggregate exposure to the pesticide to
the acute population adjusted dose
(aPAD) and chronic population adjusted
dose (cPAD). The aPAD and cPAD are
calculated by dividing the LOC by all
applicable UFs. Short-, intermediate-,
and long-term risks are evaluated by
comparing aggregate exposure to the
LOC to ensure that the margin of
exposure (MOE) called for by the
product of all applicable UFs is not
exceeded.
For non-threshold risks, the Agency
assumes that any amount of exposure
will lead to some degree of risk and
estimates risk in terms of the probability
of occurrence of additional adverse
cases. Generally, cancer risks are
considered non-threshold. For more
information on the general principles
EPA uses in risk characterization and a
complete description of the risk
assessment process, see https://
www.epa.gov/fedrgstr/EPA-PEST/1997/
November/Day-26/p30948.htm.
A summary of the toxicological
endpoints for methoxyfenozide used for
human risk assessment can be found at
https://www.regulations.gov in document
‘‘Methoxyfenozide. Human Health Risk
Assessment for Proposed Use on Sweet
Potato, Blueberry, Dry Bean, Grass,
Peanut, Green Onion, Avocado, Guava,
Alfalfa and Clover. PC Code:121027,
Petition No: 6E7086, 7E7218, and
6F7135. DP Num: 331948, 340540, and
371933’’ at page 30 in docket ID number
EPA–HQ–OPP–2007–0495.
C. Exposure Assessment
1. Dietary exposure from food and
feed uses. In evaluating dietary
exposure to methoxyfenozide, EPA
considered exposure under the
petitioned-for tolerances as well as all
existing methoxyfenozide tolerances in
40 CFR 180.544. EPA assessed dietary
exposures from methoxyfenozide in
food as follows:
i. Acute exposure. Quantitative acute
dietary exposure and risk assessments
are performed for a food-use pesticide,
if a toxicological study has indicated the
possibility of an effect of concern
occurring as a result of a 1–day or single
exposure.
No such effects were identified in the
toxicological studies for
methoxyfenozide; therefore, a
quantitative acute dietary exposure
assessment is unnecessary.
ii. Chronic exposure. In conducting
the chronic dietary exposure assessment
EPA used the food consumption data
from the USDA 1994–1996 and 1998
CSFII. As to residue levels in food, EPA
assumed all foods for which there are
tolerances were treated and contain
tolerance-level residues.
PO 00000
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11823
iii. Cancer. Methoxyfenozide is not
likely to be carcinogenic to humans;
therefore, a cancer exposure assessment
was not conducted.
iv. Anticipated residue and percent
crop treated. Anticipated residues/PCT
data were not needed to refine the risk
assessment so they were not used.
2. Dietary exposure from drinking
water. Methoxyfenozide is expected to
be a ground water and surface water
contaminant primarily due to its
persistence in the environment.
Based on the Pesticide Root Zone
Model/Exposure Analysis Modeling
System (PRZM/EXAMS) and Screening
Concentration in Ground Water (SCIGROW) models, the estimated
environmental concentrations (EECs) of
methoxyfenozide for acute exposures
are estimated to be 43 parts per billion
(ppb) for surface water and 7.43 ppb for
ground water. The EECs for chronic
exposures are estimated to be 33.1 ppb
for surface water and <7.43 ppb for
ground water.
Modeled estimates of drinking water
concentrations were directly entered
into the dietary exposure model. For
acute dietary risk assessment, the water
concentration value of 43 ppb was used
to access the contribution to drinking
water. For chronic dietary risk
assessment, the water concentration of
value 33.1 ppb was used to access the
contribution to drinking water.
3. From non-dietary exposure. The
term ‘‘residential exposure’’ is used in
this document to refer to nonoccupational, non-dietary exposure
(e.g., for lawn and garden pest control,
indoor pest control, termiticides, and
flea and tick control on pets).
Methoxyfenozide is not registered for
use on any sites that would result in
residential exposure.
4. Cumulative effects from substances
with a common mechanism of toxicity.
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
methoxyfenozide and any other
substances and methoxyfenozide does
not appear to produce a toxic metabolite
produced by other substances. For the
purposes of this tolerance action,
therefore, EPA has not assumed that
methoxyfenozide has a common
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mechanism of toxicity with other
substances. For information regarding
EPA’s efforts to determine which
chemicals have a common mechanism
of toxicity and to evaluate the
cumulative effects of such chemicals,
see the policy statements released by
EPA’s Office of Pesticide Programs
concerning common mechanism
determinations and procedures for
cumulating effects from substances
found to have a common mechanism on
EPA’s website at https://www.epa.gov/
pesticides/cumulative.
D. Safety Factor for Infants and
Children
1. In general. Section 408 of FFDCA
provides that EPA shall apply an
additional tenfold margin of safety for
infants and children in the case of
threshold effects to account for prenatal
and postnatal toxicity and the
completeness of the database on toxicity
and exposure unless EPA determines
based on reliable data that a different
margin of safety will be safe for infants
and children. This additional margin of
safety is commonly refered to as the
FQPA safety factor. In applying this
provision, EPA either retains the default
value of 10X when reliable data do not
support the choice of a different factor,
or, if reliable data are available, EPA
uses a different additional FQPA safety
factor value based on the use of
traditional UFs and/or special FQPA
safety factors, as appropriate.
2. Prenatal and postnatal sensitivity.
There is not a concern for prenatal and/
or postnatal toxicity resulting from
exposure to methoxyfenozide. The
prenatal and postnatal toxicology
database for methoxyfenozide includes
rat and rabbit developmental toxicity
studies and a 2–generation reproduction
toxicity study in rats. There was no
quantitative or qualitative evidence of
increased susceptibility of rats or rabbit
fetuses to in utero exposure in the
developmental studies; similarly, there
was no evidence of increased
susceptibility of rat pups following
prenatal/postnatal exposure in the 2–
generation reproduction study.
3. Conclusion. The FQPA SF for the
protection of infants and children be
removed (i.e. reduced to 1x) for
methoxyfenozide for the following
reasons:
i. The toxicology database for
methoxyfenozide is complete for
assessment of potential hazard to infants
and children.
ii. Based on weight-of-the-evidence
considerations, EPA determined that a
developmental neurotoxicity study in
rats is not required to support the
registration of methoxyfenozide.
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iii. In developmental toxicity studies
in rats and rabbits, no increased
susceptibility in fetuses as compared to
maternal animals was observed
following in utero exposures.
iv. In a 2–generation reproduction
study in rats, no increased susceptibility
in pups as compared to adults was
observed following in utero and
postnatal exposures.
v. The exposure assessments will not
underestimate the potential dietary
(food and drinking water) or nondietary
exposures for infants and children from
the use of methoxyfenozide. The
chronic dietary food exposure
assessment utilizes tolerance level
residues and assumes 100 PCT.
Conservative ground water and surface
water modeling estimates were used.
These assessments will not
underestimate the exposure and risks
posed by methoxyfenozide.
E. Aggregate Risks and Determination of
Safety
Safety is assessed for acute and
chronic risks by comparing aggregate
exposure to the pesticide to the aPAD
and cPAD. The aPAD and cPAD are
calculated by dividing the LOC by all
applicable UFs. For linear cancer risks,
EPA calculates the probability of
additional cancer cases given aggregate
exposure. Short-, intermediate- and logterm risks are evaluated by comparing
aggregate exposure to the LOC to ensure
that the MOE called for by the product
of all applicable UTs is not exceeded.
1. Acute risk. No acute risk is
expected from exposure to
methoxyfenozide since no acute
endpoints were identified for the
general U.S. population (including
infants and children) or the females 1350 years old population subgroup.
2. Chronic risk. Using the exposure
assumptions described in this unit for
chronic exposure, EPA has concluded
that exposure to methoxyfenozide from
food and water will utilize 56% of the
cPAD for the most highly exposed
population group, children 1-2 years
old. There are no residential uses for
methoxyfenozide.
3. Short-term risk. Short-term
aggregate exposure takes into account
residential exposure plus chronic
exposure to food and water (considered
to be a background exposure level).
Methoxyfenozide is not registered for
use on any sites that would result in
residential exposure. Therefore, the
aggregate risk is the sum of the risk from
food and water.
4. Intermediate-term risk.
Intermediate-term aggregate exposure
takes into account residential exposure
plus chronic exposure to food and water
PO 00000
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Fmt 4700
Sfmt 4700
(considered to be a background
exposure level).
Methoxyfenozide is not registered for
use on any sites that would result in
residential exposure. Therefore, the
aggregate risk is the sum of the risk from
food and water, which do not exceed
the Agency’s level of concern.
5. Aggregate cancer risk for U.S.
population. Methoxyfenozide is
classified as a ‘‘not likely’’ human
carcinogen and thus is not expected to
pose a cancer risk to humans.
6. Determination of safety. Based on
these risk assessments, 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
methoxyfenozide residues.
IV. Other Considerations
A. Analytical Enforcement Methodology
Adequate enforcement methodology
(high pressure liquid chromatography
with mass spectrometry (HPLC/MS)) 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; e-mail address:
residuemethods@epa.gov.
B. International Residue Limits
There are currently no Codex,
Canadian or Mexican MRLs for
methoxyfenozide, so there are no
international harmonization issues
associated with this action.
C. Response to Comments
Public comments were received from
a citizen who objected to the proposed
tolerances because ‘‘methoxyfenozide
harms fish and birds so that they die’’
and also opposes ‘‘any exemption or
residue left on plants after use from this
product.’’ The comments contained no
scientific data or evidence to rebut the
Agency’s conclusion that there is a
reasonable certainty that no harm will
result from human or environmental
exposure to methoxyfenozide. EPA has
responded to similar comments on
numerous previous occasions. (January
7, 2005, 70 FR 1349) (October 29, 2004,
69 FR 63083).
D. Explanation of Tolerance Revisions
The tolerances established here have
been modified in some instances from
the tolerances originally proposed in the
notices of filing. These modifications
have been based upon specific data, as
described in unit IV.D. The data
indicate that the requested tolerance on
dry beans at 0.15 ppm is not appropriate
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since the field trial data indicate that
residues could be higher than the
tolerance request. Therefore, a more
appropriate tolerance is being
established for the residues of
methoxyfenozide on bean, dry at 0.24
ppm. The data for peanut hay are
adequate. EPA’s Review indicates that
the requested tolerance of 60 ppm is not
appropriate. Therefore, a more
appropriate tolerance is being
established for the residues of
methoxyfenozide on peanut, hay at 55.0
ppm. The data for animal feed,
nongrass, group 18, forage and hay are
adequate. EPA’s Review indicates that
the requested tolerances are not
appropriate. Residue field trial data
from representative crops should be
analyzed separately and the highest
result used for tolerance setting
purposes. This was not done. A more
appropriate tolerance is being
established for the residues of
methoxyfenozide on animal feed,
nongrass, group 18, forage at 50 ppm,
and hay at 150 ppm. The only processed
commodities of regulatory concern for
this petition are peanut meal and oil. A
study was conducted using a 3x
exaggerated application rate to the
peanut raw agricultural commodity and
simulated commercial processing to
produce the peanut processed
commodities. Results of the study
indicate that residues of
methoxyfenozide are not expected to
concentrate in peanut meal but do
concentrate 3x in oil. The requested
tolerance level for peanut oil is
inadequate. Using the highest average
field trial values from the submitted
field trial data and the concentration
factor for peanut oil, the tolerance level
should be 0.04 ppm.
IR-4 petitioned for individual
tolerances on green onion, fresh chive
leaves, fresh Chinese chive leaves,
elegans hosta, fritillaria leaves, kurrat,
Lady’s leek, leek, wild leek, Beltsville
bunching onion, fresh onion, macrostem
onion, tree onion tops, Welsh onion
tops, and fresh shallot leaves at 5.0 ppm
(PP 7E7128) as well as for a tolerance for
bushberry subgroup 13B and individual
tolerances on aronia berry, buffalo
currant, Chilean guava, European
barberry, highbush cranberry,
honeysuckle, jostaberry, juneberry,
lingonberry, native currant, salal, and
sea buckthorn (PP 6E7086).
In the Federal Register of December 7,
2007 (72 FR 69150) (FRL–8340–6), EPA
issued a final rule that revised the crop
grouping regulations. As part of this
action, EPA expanded and revised bulb
vegetables group 3. Changes to crop
group 3 (bulb vegetables) included
adding new commodities, creating
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14:21 Mar 04, 2008
Jkt 214001
subgroups for bulb and green onions,
and changing the name of one of the
representative commodities from
‘‘onion, dry bulb’’ to ‘‘onion, bulb.’’ EPA
also expanded and revised berries group
13. Changes to crop group 13 (berries)
included adding new commodities,
revising existing subgroups and creating
new subgroups (including a bushberry
subgroup 13-07B consisting of the
commodities requested in PP 6E7086
and cultivars, varieties, and/or hybrids
of these).
EPA indicated in the December 7,
2007 final rule as well as the earlier May
23, 2007 proposed rule (72 FR 28920)
(FRL–8126–1) that, for existing petitions
for which a Notice of Filing had been
published, the Agency would attempt to
conform these petitions to the rule.
Therefore, consistent with this rule,
EPA is establishing tolerances on onion,
green, subgroup 3-07B and bushberry
subgroup 13-07B.
EPA concludes it is reasonable to
revise the petitioned-for tolerances so
that they agree with the recent crop
grouping revisions because:
1. Although the subgroups are new
the commodities in the new group were
proposed as individual tolerances and
the added commodities are closely
related minor crops which contribute
little to overall dietary or aggregate
exposure and risk; and
2. Methoxyfenozide exposure from
these added commodities was
considered when EPA conducted the
dietary and aggregate risk assessments
supporting this action.
V. Conclusion
Therefore, tolerances are established
for residues of methoxyfenozide;
benzoic acid, 3-methoxy-2-methyl-2(3,5-dimethylbenzoyl)-2-(1,1dimethylethyl)hydrazide, in or on the
food commodities acerola at 0.4 ppm;
animal feeds, nongrass, group 18, forage
at 50.0 ppm; animal feeds, nongrass,
group 18, hay at 150.0 ppm; avocado at
0.6 ppm; bean, dry, seed at 0.24 ppm;
bushberry subgroup 13-07B at 3.0 ppm;
canistel at 0.6 ppm; feijoa at 0.4 ppm;
grass, forage, fodder, and hay group 17,
forage at 18.0 ppm; grass, forage, fodder,
and hay, group 17, hay at 30.0 ppm;
guava at 0.4 ppm; jaboticaba at 0.4 ppm;
mango at 0.6 ppm; onions, green,
subgroup 3-07B at 5.0 ppm; papaya at
0.6 ppm; passionfruit at 0.4 ppm;
peanut at 0.02 ppm; peanut, hay at 55
ppm; peanut oil at 0.04 ppm; sapodilla
at 0.6 ppm; sapote, black at 0.6 ppm;
sapote, mamey at 0.6 ppm; star apple at
0.6 ppm; starfruit at 0.4 ppm; vegetable,
tuberous and corm, except potato, sub
group 1D at 0.02 ppm; wax jambu at 0.4
ppm.
PO 00000
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Fmt 4700
Sfmt 4700
11825
Time-limited tolerances are
established for the indirect or
inadvertent residues for
methoxyfenozide in or on vegetable,
bulb, group 3 at 0.2 ppm; vegetable,
leaves of root and tuber, group 2 at 0.2
ppm; and vegetable, root and tuber,
group 1 at 0.1 ppm; and the combined
residues of methoxyfenozide; benzoic
acid, 3-methoxy-2-methyl-, 2-(3,5dimethylbenzoyl)-2-(1,1-dimethylethyl)
hydrazide and its metabolites RH117,236 free phenol of
methoxyfenozide; 3,5-dimethylbenzoic
acid N-tert-butyl-N’-(3-hydroxy-2methylbenzoyl) hydrazide, RH-151,055
glucose conjugate of RH-117,236; 3,5dimethyl benzoic acid N-tert-butyl-N-[3
([beta]-D-glucopyranosyloxy)-2methylbenzoyl]-hydrazide and RH152,072 the malonylglycosyl conjugate
of RH 117,236 in or on the food
commodities animal feed, nongrass,
group 18 at 10.0 ppm; grain, cereal,
forage, fodder and straw, group 16 at
10.0 ppm; grass forage, fodder and hay,
group 17 at 10.0 ppm; herb and spice,
group 19 at 10.0 ppm; vegetable, foliage
of legume, group 7 at 10.0 ppm; and
vegetable, legume, group 6 at 0.10 ppm.
VI. Statutory and Executive Order
Reviews
This final rule establishes a tolerance
under section 408(d) of FFDCA 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 rule has
been exempted from review under
Executive Order 12866, this rule is not
subject to Executive Order 13211,
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 final rule 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 section 408(d) of FFDCA, such as
the tolerance in this final rule, do not
require the issuance of a proposed rule,
the requirements of the Regulatory
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Flexibility Act (RFA) (5 U.S.C. 601 et
seq.) do not apply.
This final rule 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 section 408(n)(4) of FFDCA. 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 6, 2000) do not apply
to this rule. In addition, This rule does
not impose any enforceable duty or
contain any unfunded mandate as
described under Title II of the Unfunded
Mandates Reform Act of 1995 (UMRA)
(Public Law 104–4).
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 of 1995
(NTTAA), Public Law 104–113, section
12(d) (15 U.S.C. 272 note).
VII. Congressional Review Act
The Congressional Review Act, 5
U.S.C. 801 et seq., generally provides
that before a rule may take effect, the
agency promulgating the rule must
submit a rule report to each House of
the Congress and to the Comptroller
General of the United States. 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 this final rule in the
Federal Register. This final rule is not
a ‘‘major rule’’ as defined by 5 U.S.C.
804(2).
yshivers on PROD1PC62 with RULES
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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Jkt 214001
Dated: February 14, 2008.
Donald R. Stubbs,
Acting Director, Registration Division, Office
of Pesticide Programs.
Therefore, 40 CFR chapter I is
amended as follows:
I
PART 180—AMENDED
1. The authority citation for part 180
continues to read as follows:
I
Authority: 21 U.S.C. 321(q), 346a and 371.
2. Section 180.544 is amended by:
i. Revising the entries ‘‘canistel’’;
‘‘mango’’; ‘‘papaya’’; ‘‘sapodilla’’;
‘‘sapote, black’’; ‘‘sapote, mamey’’; and
‘‘star apple’’ in paragraph (a)(1).
I ii. Alphabetically adding commodities
to the table in paragraph (a)(1).
I iii. Removing the text from paragraph
(b) and reserving the heading.
I iv. Revising the tables in paragraphs
(d)(1) and (d)(2) to read as follows:
I
I
§ 180.544 Methoxyfenozide; tolerances for
residues.
Parts per million
Acerola ............................
*
*
*
Animal feed, nongrass,
group 18, forage .........
Animal feed, nongrass,
group 18, hay ..............
*
*
*
Avocado ..........................
Bean, dry, seed ..............
*
*
*
Bushberry subgroup 1307B ..............................
Canistel ...........................
*
*
*
Feijoa ..............................
*
*
*
Grass, forage, fodder
and hay, group 17, forage ..............................
Grass, forage, fodder
and hay, group 17, hay
Guava .............................
*
*
*
Jaboticaba ......................
*
*
*
Mango .............................
*
*
*
Onion, green, subgroup
3-07B ...........................
Papaya ............................
Passionfruit .....................
*
*
*
Peanut ............................
Peanut, hay ....................
Peanut, oil .......................
*
*
*
Sapodilla .........................
Sapote, black ..................
Sapote, mamey ..............
*
*
*
Star apple .......................
Starfruit ...........................
PO 00000
Frm 00016
Fmt 4700
Parts per million
*
*
*
Vegetable, tuberous and
corm, except potato,
subgroup 1D ...............
Wax jambu ......................
*
*
0.02
0.4
(b) Section 18 emergency exemptions.
[Reserved]
(c) Tolerances with regional
registrations. [Reserved]
(d) * * *
(1) * * *
Commodity
Parts per
million
Vegetable, bulb,
group 3-07 .....
Vegetable,
leaves of root
and tuber,
group 2 ..........
Vegetable, root
and tuber,
group 1 ..........
Expiration/
revocation
date
0.20
9/30/10
0.20
9/30/10
0.10
9/30/10
(2) * * *
(a) General. (1) * * *
Commodity
Commodity
Commodity
Parts per
million
0.4
*
*
50.0
*
*
150.0
*
0.6
0.24
*
3.0
0.6
*
*
0.4
*
*
18.0
*
*
*
30.0
0.4
*
0.4
*
0.6
*
Animal feed,
non-grass,
group 18 ........
Grain, cereal,
forage, fodder
and straw,
group 16 ........
Grass, forage,
fodder and
hay, group 17
Herb and spice,
group 19 ........
Vegetable, foliage of legume, group 7
Vegetable, legume, group 6
Expiration/
revocation
date
10.0
9/30/10
10.0
9/30/10
10.0
9/30/10
10.0
9/30/10
10.0
9/30/10
0.10
9/30/10
[FR Doc. E8–4027 Filed 3–4–08; 8:45 am]
BILLING CODE 6560–50–S
ENVIRONMENTAL PROTECTION
AGENCY
40 CFR Part 180
5.0
0.6
0.4
*
*
*
Sfmt 4700
*
0.02
55.0
0.04
*
0.6
0.6
0.6
*
0.6
0.4
[EPA–HQ–OPP–2007–0308; FRL–8352–5]
Flumioxazin; Pesticide Tolerance
Environmental Protection
Agency (EPA).
ACTION: Final rule.
AGENCY:
SUMMARY: This regulation establishes a
tolerance for residues of flumioxazin in
or on alfalfa, forage; alfalfa, hay;
asparagus; bean, dry seed; bushberry
subgroup 13-07B; melon, subgroup 9A;
E:\FR\FM\05MRR1.SGM
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Agencies
[Federal Register Volume 73, Number 44 (Wednesday, March 5, 2008)]
[Rules and Regulations]
[Pages 11820-11826]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E8-4027]
-----------------------------------------------------------------------
ENVIRONMENTAL PROTECTION AGENCY
40 CFR Part 180
[EPA-HQ-OPP-2007-0495; FRL-8352-2]
Methoxyfenozide; Pesticide Tolerances and Time-Limited Pesticide
Tolerances
AGENCY: Environmental Protection Agency (EPA).
ACTION: Final rule.
-----------------------------------------------------------------------
SUMMARY: This regulation establishes tolerances for residues of
methoxyfenozide per se; benzoic acid, 3-methoxy-2-methyl-2-(3,5-
dimethylbenzoyl)-2-(1,1-dimethylethyl)hydrazide in or on the food
commodities acerola; animal feed, nongrass, group 18, forage; animal
feed, nongrass, group 18, hay; avocado; bean,
[[Page 11821]]
dry, seed; bushberry subgroup 13-07B; canistel; feijoa; grass, forage,
fodder and hay, group 17, forage; grass, forage, fodder and hay, group
17, hay; guava; jaboticaba; kurrat; mango; onion, green, subgroup 3-
07B; papaya; passionfruit; peanut; peanut, hay; peanut oil; sapodilla;
sapote, black; sapote, mamey; star apple; starfruit; vegetable,
tuberous and corm, except potato, sub group 1D; and wax jambu. This
regulation also establishes time-limited tolerances for indirect or
inadvertent residues of methoxyfenozide; benzoic acid, 3-methoxy-2-
methyl-, 2-(3,5-dimethylbenzoyl)-2-(1,1-dimethylethyl) hydrazide and
indirect or inadvertent combined residues of methoxyfenozide and its
metabolites RH-117,236 free phenol of methoxyfenozide; 3,5-
dimethylbenzoic acid N-tert-butyl-N'-(3-hydroxy-2-methylbenzoyl)
hydrazide, RH-151,055 glucose conjugate of RH-117,236; 3,5-dimethyl
benzoic acid N-tert-butyl-N-[3 ([beta]-D-glucopyranosyloxy)-2-
methylbenzoyl]-hydrazide and RH-152,072 the malonylglycosyl conjugate
of RH 117,236 in or on the food commodities animal feed, nongrass,
group 18; grain, cereal, forage, fodder and straw, group 16; grass
forage, fodder, and hay, group 17; herb and spice, group 19; vegetable,
bulb, group 3-07; vegetable, foliage of legume, group 7; vegetable,
leaves of root and tuber, group 2; vegetable, legume, group 6; and
vegetable, root and tuber, group 1. Dow AgroSciences LLC and
Interregional Research Project Number 4 (IR-4) requested these
tolerances under the Federal Food, Drug, and Cosmetic Act (FFDCA). The
time-limited tolerances will expire on September 30, 2010.
DATES: This regulation is effective March 5, 2008. Objections and
requests for hearings must be received on or before May 5, 2008, 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: EPA has established a docket for this action under docket
identification (ID) number EPA-HQ-OPP-2007-0495. To access the
electronic docket, go to https://www.regulations.gov, select ``Advanced
Search,'' then ``Docket Search.'' Insert the docket ID number where
indicated and select the ``Submit'' button. Follow the instructions on
the regulations.gov website to view the docket index or access
available documents. All documents in the docket are listed in the
docket index available in regulations.gov. Although listed in the
index, some information is not publicly available, e.g., Confidential
Business Information (CBI) or other information whose disclosure is
restricted by statute. Certain other material, such as copyrighted
material, is not placed on the Internet and will be publicly available
only in hard copy form. Publicly available docket materials are
available either in the electronic docket at https://
www.regulations.gov, or, if only available in hard copy, at the OPP
Public Docket, in Rm. S-4400, One Potomac Yard (South Bldg.), 2777 S.
Crystal Dr., Arlington, VA. The Docket Facility is open from 8:30 a.m.
to 4 p.m., Monday through Friday, excluding legal holidays. The Docket
Facility telephone number is (703) 305-5805.
FOR FURTHER INFORMATION CONTACT: Mark Suarez, Registration Division
(7505P), Office of Pesticide Programs, Environmental Protection Agency,
1200 Pennsylvania Ave., NW., Washington, DC 20460-0001; telephone
number: (703) 305-0120; e-mail address: suarez.mark@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.
Potentially affected entities may include, but are not limited to those
engaged in the following activities:
Crop production (NAICS code 111), e.g., agricultural
workers; greenhouse, nursery, and floriculture workers; farmers.
Animal production (NAICS code 112), e.g., cattle ranchers
and farmers, dairy cattle farmers, livestock farmers.
Food manufacturing (NAICS code 311) , e.g., agricultural
workers; farmers; greenhouse, nursery, and floriculture workers;
ranchers; pesticide applicators.
Pesticide manufacturing (NAICS code 32532), e.g.,
agricultural workers; commercial applicators; farmers; greenhouse,
nursery, and floriculture workers; residential users.
This listing is not intended to be exhaustive, but rather provides
a guide for readers regarding entities likely to be affected by this
action. Other types of entities not listed in this unit could also be
affected. The North American Industrial Classification System (NAICS)
codes have been provided to assist you and others in determining
whether this action might apply to certain entities. If you have any
questions regarding the applicability of this action to a particular
entity, consult the person listed under FOR FURTHER INFORMATION
CONTACT.
B. How Can I Access Electronic Copies of this Document?
In addition to accessing an electronic copy of this Federal
Register document through the electronic docket at https://
www.regulations.gov, you may access this Federal Register document
electronically through the EPA Internet under the ``Federal Register''
listings at https://www.epa.gov/fedrgstr. You may also access a
frequently updated electronic version of 40 CFR part 180 through the
Government Printing Office's pilot e-CFR site at https://
www.gpoaccess.gov/ecfr.
C. Can I File an Objection or Hearing Request?
Under section 408(g) of FFDCA, as amended by FQPA, any person may
file an objection to any aspect of this regulation and may also request
a hearing on those objections. The EPA procedural regulations which
govern the submission of objections and requests for hearings appear in
40 CFR part 178. 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-2007-0495 in the subject line on the first page of
your submission. All requests must be in writing, and must be mailed or
delivered to the Hearing Clerk on or before May 5, 2008.
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 that does not contain any CBI for inclusion in the public
docket that is described in ADDRESSES. Information not marked
confidential pursuant to 40 CFR part 2 may be disclosed publicly by EPA
without prior notice. Submit your copies, identified by docket ID
number EPA-HQ-OPP-2007-0495, by one of the following methods:
Federal eRulemaking Portal: https://www.regulations.gov.
Follow the on-line instructions for submitting comments.
Mail: Office of Pesticide Programs (OPP) Regulatory Public
Docket (7502P), Environmental Protection Agency, 1200 Pennsylvania
Ave., NW., Washington, DC 20460-0001.
Delivery: OPP Regulatory Public Docket (7502P),
Environmental Protection Agency, Rm. S-4400, One Potomac Yard (South
Bldg., 2777 S. Crystal Dr., Arlington, VA. Deliveries are only accepted
during the Docket's normal hours of operation (8:30 a.m. to 4 p.m.,
Monday through Friday, excluding legal holidays). Special arrangements
should be made for
[[Page 11822]]
deliveries of boxed information. The Docket Facility telephone number
is (703) 305-5805.
II. Petition for Tolerances
In the Federal Register of October 20, 2006 (71 FR 61971) (FRL-
8098-6), August 1, 2007 (72 FR 42072) (FRL-8138-1), and October 24,
2007 (72 FR 60367) (FRL-8154-1), EPA issued notices pursuant to section
408(d)(3) of FFDCA, 21 U.S.C. 346a(d)(3), announcing the filing of
pesticide petitions (PPs 6E7086, 7E7218, 6F7135, and 0F6201) by, Dow
AgroSciences LLC, Zionsville Road -Indianapolis, IN 46268 (PPs 6F7135
and 0F6201) and IR-4, 500 College Road East, Suite 201 W., Princeton,
NJ 08540 (PPs 7E7218 and 6E7086). The petitions requested that 40 CFR
180.544 be amended by establishing tolerances for residues of the
insecticide, methoxyfenozide, in or on the food commodities acerola at
0.4 parts per million (ppm) (PP 7E7218); arionia berry at 3.0 ppm (PP
6E7086); avocado at 0.6 ppm (PP 7E7218); bean, dry, seed at 0.15 ppm
(PP 6E7086); blueberry, lowbush at 3.0 ppm (PP 6E7086); buffalo currant
at 3.0 ppm (PP 6E7086); bushberry subgroup 13B at 3.0 ppm (PP 6E7086);
canistel at 0.6 ppm (PP 7E7218); Chilean guava at 3.0 ppm (PP 6E7086);
chive, Chinese, fresh leaves at 5.0 ppm (PP 7E7218); chive, fresh
leaves at 5.0 ppm (PP 7E7218); elegans hosta at 5.0 ppm (PP 7E7218);
European barberry at 3.0 ppm (PP 6E7086); feijoa at 0.4 ppm (PP
7E7218); fritillaria leaves at 5.0 ppm (PP 7E7218); grass forage,
fodder, and hay group 17, forage at 18.0 ppm (PP 6E7086); grass forage,
fodder, and hay, group 17, hay at 30.0 ppm (PP 6E7086); guava at 0.4
ppm (PP 7E7218); highbush cranberry at 3.0 ppm (PP 6E7086); honeysuckle
at 3.0 ppm (PP 6E7086); jaboticaba at 0.4 ppm (PP 7E7218); jostaberry
at 3.0 ppm (PP 6E7086); juneberry at 3.0 ppm (PP 6E7086); kurrat at 5.0
ppm (PP 7E7218); Lady's leek at 5.0 ppm (PP 7E7218); leek at 5.0 ppm
(PP 7E7218); leek, wild at 5.0 ppm (PP 7E7218); lingonberry at 3.0 ppm
(PP 6E7086); mango at 0.6 ppm (PP 7E7218); native currant at 3.0 ppm
(PP 6E7086); nongrass animal feeds, group 18, forage at 35.0 ppm (PP
6F7135); nongrass animal feeds, group 18, hay at 85.0 ppm (PP 6F7135);
onion, Beltsville bunching at 5.0 ppm (PP 7E7218); onion, fresh at 5.0
ppm (PP 7E7218); onion, green at 5.0 ppm (PP 7E7218); onion, macrostem
at 5.0 ppm (PP 7E7218); onion, tree, tops at 5.0 ppm (PP 7E7218);
onion, Welsh, tops at 5.0 ppm (PP 7E7218); papaya at 0.6 ppm (PP
7E7218); passionfruit at 0.4 ppm (PP 7E7218); peanut at 0.02 ppm (PP
6E7086); peanut, hay at 60 ppm (PP 6E7086); peanut oil at 0.09 ppm (PP
6E7086); salal at 3.0 ppm (PP 6E7086); sapodilla at 0.6 ppm (PP
7E7218); sapote, black at 0.6 ppm (PP 7E7218); sapote, mamey at 0.6 ppm
(PP 7E7218); sea buckthorn at 3.0 ppm (PP 6E7086); shallot, fresh
leaves at 5.0 ppm (PP 7E7218); star apple at 0.6 ppm (PP 7E7218);
starfruit at 0.4 ppm (PP 7E7218); vegetable, tuberous and corm, except
potato, sub group 1D at 0.02 ppm (PP 6E7086); wax jambu at 0.4 ppm (PP
7E7218). In the petition 0F6201, Dow requested that tolerances that
expired on September 30, 2007 be re-established for indirect or
inadvertent residues of methoxyfenozide; benzoic acid, 3-methoxy-2-
methyl-, 2-(3,5-dimethylbenzoyl)-2-(1,1-dimethylethyl) hydrazide and
indirect or inadvertent combined residues of methoxyfenozide; benzoic
acid, 3-methoxy-2-methyl-, 2-(3,5-dimethylbenzoyl)-2-(1,1-
dimethylethyl) hydrazide and its metabolites RH-117,236 free phenol of
methoxyfenozide; 3,5-dimethylbenzoic acid N-tert-butyl-N'-(3-hydroxy-2-
methylbenzoyl) hydrazide, RH-151,055 glucose conjugate of RH-117,236;
3,5-dimethyl benzoic acid N-tert-butyl-N-[3 ([beta]-D-
glucopyranosyloxy)-2-methylbenzoyl]-hydrazide and RH-152,072 the
malonylglycosyl conjugate of RH 117,236 in or on the food commodities
grain, cereal, forage, fodder, and straw, group 16 at 10.0 ppm; grass
forage, fodder, and hay, group 17 at 10.0 ppm; herb and spice, group 19
at 10.0 ppm; nongrass animal feeds crop group 18 at 10.0 ppm;
vegetable, bulb, group 3 at 0.2 ppm; vegetable, foliage of legume,
group 7 at 10.0 ppm; vegetable, leaves of root and tuber, group 2 at
0.2 ppm; vegetable, legume, group 6 at 0.1 ppm; and vegetable, root and
tuber, group 1 at 0.1 ppm. Those notices referenced summaries of the
petitions prepared by Dow AgroSciences LLC and IR-4, the registrants,
which are available to the public in the docket, https://
www.regulations.gov. Comments were received on the notices of filing.
EPA's response to these comments is discussed in Unit IV.C. The time-
limited tolerances will expire on September 30, 2010.
Based upon review of the data supporting the petition, EPA has
modified the tolerance expression for the food commodities bean, dry,
seed to 0.24 ppm (PP 6E7086); animal feeds, nongrass, group 18, forage
to 50.0 ppm (PP 6F7135); animal feeds, nongrass, group 18, hay to 150.0
ppm (PP 6F7135); onions, green, subgroup 3-07B at 5.0 ppm (PP 7E7218);
peanut, hay to 55 ppm (PP 6E7086); peanut oil to 0.04 ppm (PP 6E7086).
The reason for these changes is explained in Unit IV.D. EPA is also
deleting all the tolerances in Sec. 180.544(b) for sorghum and soybean
commodities that are no longer needed since they have expired. The
deletions under Sec. 180.544(b) are time-limited tolerances that were
established under section 18 emergency exemptions that have since
expired.
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. . .
.''
EPA performs a number of analyses to determine the risks from
aggregate exposure to pesticide residues. For further discussion of the
regulatory requirements of section 408 of FFDCA and a complete
description of the risk assessment process, see https://www.epa.gov/
fedrgstr/EPA-PEST/1997/November/Day-26/p30948.htm.
Consistent with section 408(b)(2)(D) of FFDCA, 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, consistent with section
408(b)(2) of FFDCA, for tolerances for the petitioned-for tolerances
for residues of methoxyfenozide on the food commodities named above.
EPA's assessment of exposures and risks associated with establishing
the tolerance follows.
A. Toxicological Profile
EPA has evaluated the available toxicity data and considered its
validity, completeness, and reliability as well as the relationship of
the results of the studies to human risk. EPA has also considered
available information
[[Page 11823]]
concerning the variability of the sensitivities of major identifiable
subgroups of consumers, including infants and children.
The toxicology studies conducted with methoxyfenozide demonstrate
that it has few or no biologically significant toxic effects at
relatively low-dose levels and only mild or no toxic effects at
relatively high-dose levels. In subchronic and chronic oral studies in
rats, the most toxicologically significant effects were mild anemia and
mild effects on the liver, thyroid gland, and adrenal gland. In
subchronic and chronic oral studies in dogs, the predominant toxic
effect was anemia, which was often accompanied by signs of a
compensatory response. Methoxyfenozide is not acutely toxic, not a
dermal sensitizer, not neurotoxic, carcinogenic or mutagenic and is not
a developmental or reproductive toxicant. There was no evidence for
increased susceptibility of rat or rabbit fetuses to in utero exposure
or rat pups to post-natal exposure to methoxyfenozide. Minimal or no
toxic effects were observed in studies in which methoxyfenozide was
administered by the dermal or inhalation routes of exposure.
Methoxyfenozide is classified as a ``not likely'' human carcinogen.
Specific information on the studies received and the nature of the
adverse effects caused by methoxyfenozide as well as the no-observed-
adverse-effect-level (NOAEL) and the lowest-observed-adverse-effect-
level (LOAEL) from the toxicity studies can be found at https://
www.regulations.gov. The referenced document is available in the docket
established by this action, which is described under ADDRESSES, and is
identified as EPA-HQ-OPP-2007-0495 in that docket.
B. Toxicological Endpoints
For hazards that have a threshold below which there is no
appreciable risk, the toxicological level of concern (LOC) is derived
from the highest dose at which no adverse effects are observed (the
NOAEL) in the toxicology study identified as appropriate for use in
risk assessment. However, if a NOAEL cannot be determined, the lowest
dose at which adverse effects of concern are identified (the LOAEL) is
sometimes used for risk assessment. Uncertainty/safety factors (UFs)
are used in conjunction with the LOC to take into account uncertainties
inherent in the extrapolation from laboratory animal data to humans and
in the variations in sensitivity among members of the human population
as well as other unknowns. Safety is assessed for acute and chronic
risks by comparing aggregate exposure to the pesticide to the acute
population adjusted dose (aPAD) and chronic population adjusted dose
(cPAD). The aPAD and cPAD are calculated by dividing the LOC by all
applicable UFs. Short-, intermediate-, and long-term risks are
evaluated by comparing aggregate exposure to the LOC to ensure that the
margin of exposure (MOE) called for by the product of all applicable
UFs is not exceeded.
For non-threshold risks, the Agency assumes that any amount of
exposure will lead to some degree of risk and estimates risk in terms
of the probability of occurrence of additional adverse cases.
Generally, cancer risks are considered non-threshold. For more
information on the general principles EPA uses in risk characterization
and a complete description of the risk assessment process, see https://
www.epa.gov/fedrgstr/EPA-PEST/1997/November/Day-26/p30948.htm.
A summary of the toxicological endpoints for methoxyfenozide used
for human risk assessment can be found at https://www.regulations.gov in
document ``Methoxyfenozide. Human Health Risk Assessment for Proposed
Use on Sweet Potato, Blueberry, Dry Bean, Grass, Peanut, Green Onion,
Avocado, Guava, Alfalfa and Clover. PC Code:121027, Petition No:
6E7086, 7E7218, and 6F7135. DP Num: 331948, 340540, and 371933'' at
page 30 in docket ID number EPA-HQ-OPP-2007-0495.
C. Exposure Assessment
1. Dietary exposure from food and feed uses. In evaluating dietary
exposure to methoxyfenozide, EPA considered exposure under the
petitioned-for tolerances as well as all existing methoxyfenozide
tolerances in 40 CFR 180.544. EPA assessed dietary exposures from
methoxyfenozide in food as follows:
i. Acute exposure. Quantitative acute dietary exposure and risk
assessments are performed for a food-use pesticide, if a toxicological
study has indicated the possibility of an effect of concern occurring
as a result of a 1-day or single exposure.
No such effects were identified in the toxicological studies for
methoxyfenozide; therefore, a quantitative acute dietary exposure
assessment is unnecessary.
ii. Chronic exposure. In conducting the chronic dietary exposure
assessment EPA used the food consumption data from the USDA 1994-1996
and 1998 CSFII. As to residue levels in food, EPA assumed all foods for
which there are tolerances were treated and contain tolerance-level
residues.
iii. Cancer. Methoxyfenozide is not likely to be carcinogenic to
humans; therefore, a cancer exposure assessment was not conducted.
iv. Anticipated residue and percent crop treated. Anticipated
residues/PCT data were not needed to refine the risk assessment so they
were not used.
2. Dietary exposure from drinking water. Methoxyfenozide is
expected to be a ground water and surface water contaminant primarily
due to its persistence in the environment.
Based on the Pesticide Root Zone Model/Exposure Analysis Modeling
System (PRZM/EXAMS) and Screening Concentration in Ground Water (SCI-
GROW) models, the estimated environmental concentrations (EECs) of
methoxyfenozide for acute exposures are estimated to be 43 parts per
billion (ppb) for surface water and 7.43 ppb for ground water. The EECs
for chronic exposures are estimated to be 33.1 ppb for surface water
and <7.43 ppb for ground water.
Modeled estimates of drinking water concentrations were directly
entered into the dietary exposure model. For acute dietary risk
assessment, the water concentration value of 43 ppb was used to access
the contribution to drinking water. For chronic dietary risk
assessment, the water concentration of value 33.1 ppb was used to
access the contribution to drinking water.
3. From non-dietary exposure. The term ``residential exposure'' is
used in this document to refer to non-occupational, non-dietary
exposure (e.g., for lawn and garden pest control, indoor pest control,
termiticides, and flea and tick control on pets).
Methoxyfenozide is not registered for use on any sites that would
result in residential exposure.
4. Cumulative effects from substances with a common mechanism of
toxicity. 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 methoxyfenozide and any
other substances and methoxyfenozide does not appear to produce a toxic
metabolite produced by other substances. For the purposes of this
tolerance action, therefore, EPA has not assumed that methoxyfenozide
has a common
[[Page 11824]]
mechanism of toxicity with other substances. For information regarding
EPA's efforts to determine which chemicals have a common mechanism of
toxicity and to evaluate the cumulative effects of such chemicals, see
the policy statements released by EPA's Office of Pesticide Programs
concerning common mechanism determinations and procedures for
cumulating effects from substances found to have a common mechanism on
EPA's website at https://www.epa.gov/pesticides/cumulative.
D. Safety Factor for Infants and Children
1. In general. Section 408 of FFDCA provides that EPA shall apply
an additional tenfold margin of safety for infants and children in the
case of threshold effects to account for prenatal and postnatal
toxicity and the completeness of the database on toxicity and exposure
unless EPA determines based on reliable data that a different margin of
safety will be safe for infants and children. This additional margin of
safety is commonly refered to as the FQPA safety factor. In applying
this provision, EPA either retains the default value of 10X when
reliable data do not support the choice of a different factor, or, if
reliable data are available, EPA uses a different additional FQPA
safety factor value based on the use of traditional UFs and/or special
FQPA safety factors, as appropriate.
2. Prenatal and postnatal sensitivity. There is not a concern for
prenatal and/or postnatal toxicity resulting from exposure to
methoxyfenozide. The prenatal and postnatal toxicology database for
methoxyfenozide includes rat and rabbit developmental toxicity studies
and a 2-generation reproduction toxicity study in rats. There was no
quantitative or qualitative evidence of increased susceptibility of
rats or rabbit fetuses to in utero exposure in the developmental
studies; similarly, there was no evidence of increased susceptibility
of rat pups following prenatal/postnatal exposure in the 2-generation
reproduction study.
3. Conclusion. The FQPA SF for the protection of infants and
children be removed (i.e. reduced to 1x) for methoxyfenozide for the
following reasons:
i. The toxicology database for methoxyfenozide is complete for
assessment of potential hazard to infants and children.
ii. Based on weight-of-the-evidence considerations, EPA determined
that a developmental neurotoxicity study in rats is not required to
support the registration of methoxyfenozide.
iii. In developmental toxicity studies in rats and rabbits, no
increased susceptibility in fetuses as compared to maternal animals was
observed following in utero exposures.
iv. In a 2-generation reproduction study in rats, no increased
susceptibility in pups as compared to adults was observed following in
utero and postnatal exposures.
v. The exposure assessments will not underestimate the potential
dietary (food and drinking water) or nondietary exposures for infants
and children from the use of methoxyfenozide. The chronic dietary food
exposure assessment utilizes tolerance level residues and assumes 100
PCT. Conservative ground water and surface water modeling estimates
were used. These assessments will not underestimate the exposure and
risks posed by methoxyfenozide.
E. Aggregate Risks and Determination of Safety
Safety is assessed for acute and chronic risks by comparing
aggregate exposure to the pesticide to the aPAD and cPAD. The aPAD and
cPAD are calculated by dividing the LOC by all applicable UFs. For
linear cancer risks, EPA calculates the probability of additional
cancer cases given aggregate exposure. Short-, intermediate- and log-
term risks are evaluated by comparing aggregate exposure to the LOC to
ensure that the MOE called for by the product of all applicable UTs is
not exceeded.
1. Acute risk. No acute risk is expected from exposure to
methoxyfenozide since no acute endpoints were identified for the
general U.S. population (including infants and children) or the females
13-50 years old population subgroup.
2. Chronic risk. Using the exposure assumptions described in this
unit for chronic exposure, EPA has concluded that exposure to
methoxyfenozide from food and water will utilize 56% of the cPAD for
the most highly exposed population group, children 1-2 years old. There
are no residential uses for methoxyfenozide.
3. Short-term risk. Short-term aggregate exposure takes into
account residential exposure plus chronic exposure to food and water
(considered to be a background exposure level).
Methoxyfenozide is not registered for use on any sites that would
result in residential exposure. Therefore, the aggregate risk is the
sum of the risk from food and water.
4. Intermediate-term risk. Intermediate-term aggregate exposure
takes into account residential exposure plus chronic exposure to food
and water (considered to be a background exposure level).
Methoxyfenozide is not registered for use on any sites that would
result in residential exposure. Therefore, the aggregate risk is the
sum of the risk from food and water, which do not exceed the Agency's
level of concern.
5. Aggregate cancer risk for U.S. population. Methoxyfenozide is
classified as a ``not likely'' human carcinogen and thus is not
expected to pose a cancer risk to humans.
6. Determination of safety. Based on these risk assessments, 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 methoxyfenozide residues.
IV. Other Considerations
A. Analytical Enforcement Methodology
Adequate enforcement methodology (high pressure liquid
chromatography with mass spectrometry (HPLC/MS)) 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;
e-mail address: residuemethods@epa.gov.
B. International Residue Limits
There are currently no Codex, Canadian or Mexican MRLs for
methoxyfenozide, so there are no international harmonization issues
associated with this action.
C. Response to Comments
Public comments were received from a citizen who objected to the
proposed tolerances because ``methoxyfenozide harms fish and birds so
that they die'' and also opposes ``any exemption or residue left on
plants after use from this product.'' The comments contained no
scientific data or evidence to rebut the Agency's conclusion that there
is a reasonable certainty that no harm will result from human or
environmental exposure to methoxyfenozide. EPA has responded to similar
comments on numerous previous occasions. (January 7, 2005, 70 FR 1349)
(October 29, 2004, 69 FR 63083).
D. Explanation of Tolerance Revisions
The tolerances established here have been modified in some
instances from the tolerances originally proposed in the notices of
filing. These modifications have been based upon specific data, as
described in unit IV.D. The data indicate that the requested tolerance
on dry beans at 0.15 ppm is not appropriate
[[Page 11825]]
since the field trial data indicate that residues could be higher than
the tolerance request. Therefore, a more appropriate tolerance is being
established for the residues of methoxyfenozide on bean, dry at 0.24
ppm. The data for peanut hay are adequate. EPA's Review indicates that
the requested tolerance of 60 ppm is not appropriate. Therefore, a more
appropriate tolerance is being established for the residues of
methoxyfenozide on peanut, hay at 55.0 ppm. The data for animal feed,
nongrass, group 18, forage and hay are adequate. EPA's Review indicates
that the requested tolerances are not appropriate. Residue field trial
data from representative crops should be analyzed separately and the
highest result used for tolerance setting purposes. This was not done.
A more appropriate tolerance is being established for the residues of
methoxyfenozide on animal feed, nongrass, group 18, forage at 50 ppm,
and hay at 150 ppm. The only processed commodities of regulatory
concern for this petition are peanut meal and oil. A study was
conducted using a 3x exaggerated application rate to the peanut raw
agricultural commodity and simulated commercial processing to produce
the peanut processed commodities. Results of the study indicate that
residues of methoxyfenozide are not expected to concentrate in peanut
meal but do concentrate 3x in oil. The requested tolerance level for
peanut oil is inadequate. Using the highest average field trial values
from the submitted field trial data and the concentration factor for
peanut oil, the tolerance level should be 0.04 ppm.
IR-4 petitioned for individual tolerances on green onion, fresh
chive leaves, fresh Chinese chive leaves, elegans hosta, fritillaria
leaves, kurrat, Lady's leek, leek, wild leek, Beltsville bunching
onion, fresh onion, macrostem onion, tree onion tops, Welsh onion tops,
and fresh shallot leaves at 5.0 ppm (PP 7E7128) as well as for a
tolerance for bushberry subgroup 13B and individual tolerances on
aronia berry, buffalo currant, Chilean guava, European barberry,
highbush cranberry, honeysuckle, jostaberry, juneberry, lingonberry,
native currant, salal, and sea buckthorn (PP 6E7086).
In the Federal Register of December 7, 2007 (72 FR 69150) (FRL-
8340-6), EPA issued a final rule that revised the crop grouping
regulations. As part of this action, EPA expanded and revised bulb
vegetables group 3. Changes to crop group 3 (bulb vegetables) included
adding new commodities, creating subgroups for bulb and green onions,
and changing the name of one of the representative commodities from
``onion, dry bulb'' to ``onion, bulb.'' EPA also expanded and revised
berries group 13. Changes to crop group 13 (berries) included adding
new commodities, revising existing subgroups and creating new subgroups
(including a bushberry subgroup 13-07B consisting of the commodities
requested in PP 6E7086 and cultivars, varieties, and/or hybrids of
these).
EPA indicated in the December 7, 2007 final rule as well as the
earlier May 23, 2007 proposed rule (72 FR 28920) (FRL-8126-1) that, for
existing petitions for which a Notice of Filing had been published, the
Agency would attempt to conform these petitions to the rule. Therefore,
consistent with this rule, EPA is establishing tolerances on onion,
green, subgroup 3-07B and bushberry subgroup 13-07B.
EPA concludes it is reasonable to revise the petitioned-for
tolerances so that they agree with the recent crop grouping revisions
because:
1. Although the subgroups are new the commodities in the new group
were proposed as individual tolerances and the added commodities are
closely related minor crops which contribute little to overall dietary
or aggregate exposure and risk; and
2. Methoxyfenozide exposure from these added commodities was
considered when EPA conducted the dietary and aggregate risk
assessments supporting this action.
V. Conclusion
Therefore, tolerances are established for residues of
methoxyfenozide; benzoic acid, 3-methoxy-2-methyl-2-(3,5-
dimethylbenzoyl)-2-(1,1-dimethylethyl)hydrazide, in or on the food
commodities acerola at 0.4 ppm; animal feeds, nongrass, group 18,
forage at 50.0 ppm; animal feeds, nongrass, group 18, hay at 150.0 ppm;
avocado at 0.6 ppm; bean, dry, seed at 0.24 ppm; bushberry subgroup 13-
07B at 3.0 ppm; canistel at 0.6 ppm; feijoa at 0.4 ppm; grass, forage,
fodder, and hay group 17, forage at 18.0 ppm; grass, forage, fodder,
and hay, group 17, hay at 30.0 ppm; guava at 0.4 ppm; jaboticaba at 0.4
ppm; mango at 0.6 ppm; onions, green, subgroup 3-07B at 5.0 ppm; papaya
at 0.6 ppm; passionfruit at 0.4 ppm; peanut at 0.02 ppm; peanut, hay at
55 ppm; peanut oil at 0.04 ppm; sapodilla at 0.6 ppm; sapote, black at
0.6 ppm; sapote, mamey at 0.6 ppm; star apple at 0.6 ppm; starfruit at
0.4 ppm; vegetable, tuberous and corm, except potato, sub group 1D at
0.02 ppm; wax jambu at 0.4 ppm.
Time-limited tolerances are established for the indirect or
inadvertent residues for methoxyfenozide in or on vegetable, bulb,
group 3 at 0.2 ppm; vegetable, leaves of root and tuber, group 2 at 0.2
ppm; and vegetable, root and tuber, group 1 at 0.1 ppm; and the
combined residues of methoxyfenozide; benzoic acid, 3-methoxy-2-methyl-
, 2-(3,5-dimethylbenzoyl)-2-(1,1-dimethylethyl) hydrazide and its
metabolites RH-117,236 free phenol of methoxyfenozide; 3,5-
dimethylbenzoic acid N-tert-butyl-N'-(3-hydroxy-2-methylbenzoyl)
hydrazide, RH-151,055 glucose conjugate of RH-117,236; 3,5-dimethyl
benzoic acid N-tert-butyl-N-[3 ([beta]-D-glucopyranosyloxy)-2-
methylbenzoyl]-hydrazide and RH-152,072 the malonylglycosyl conjugate
of RH 117,236 in or on the food commodities animal feed, nongrass,
group 18 at 10.0 ppm; grain, cereal, forage, fodder and straw, group 16
at 10.0 ppm; grass forage, fodder and hay, group 17 at 10.0 ppm; herb
and spice, group 19 at 10.0 ppm; vegetable, foliage of legume, group 7
at 10.0 ppm; and vegetable, legume, group 6 at 0.10 ppm.
VI. Statutory and Executive Order Reviews
This final rule establishes a tolerance under section 408(d) of
FFDCA 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 rule has been
exempted from review under Executive Order 12866, this rule is not
subject to Executive Order 13211, 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 final rule 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 section 408(d) of FFDCA, such as the tolerance in
this final rule, do not require the issuance of a proposed rule, the
requirements of the Regulatory
[[Page 11826]]
Flexibility Act (RFA) (5 U.S.C. 601 et seq.) do not apply.
This final rule 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 section 408(n)(4) of FFDCA. 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 6, 2000) do not apply to this rule. In addition, This
rule does not impose any enforceable duty or contain any unfunded
mandate as described under Title II of the Unfunded Mandates Reform Act
of 1995 (UMRA) (Public Law 104-4).
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 of 1995 (NTTAA), Public Law 104-113, section 12(d) (15 U.S.C. 272
note).
VII. Congressional Review Act
The Congressional Review Act, 5 U.S.C. 801 et seq., generally
provides that before a rule may take effect, the agency promulgating
the rule must submit a rule report to each House of the Congress and to
the Comptroller General of the United States. 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 this final rule in the Federal
Register. This final rule 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: February 14, 2008.
Donald R. Stubbs,
Acting 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. Section 180.544 is amended by:
0
i. Revising the entries ``canistel''; ``mango''; ``papaya'';
``sapodilla''; ``sapote, black''; ``sapote, mamey''; and ``star apple''
in paragraph (a)(1).
0
ii. Alphabetically adding commodities to the table in paragraph (a)(1).
0
iii. Removing the text from paragraph (b) and reserving the heading.
0
iv. Revising the tables in paragraphs (d)(1) and (d)(2) to read as
follows:
Sec. 180.544 Methoxyfenozide; tolerances for residues.
(a) General. (1) * * *
------------------------------------------------------------------------
Commodity Parts per million
------------------------------------------------------------------------
Acerola.............................................. 0.4
* * * * *
Animal feed, nongrass, group 18, forage.............. 50.0
Animal feed, nongrass, group 18, hay................. 150.0
* * * * *
Avocado.............................................. 0.6
Bean, dry, seed...................................... 0.24
* * * * *
Bushberry subgroup 13-07B............................ 3.0
Canistel............................................. 0.6
* * * * *
Feijoa............................................... 0.4
* * * * *
Grass, forage, fodder and hay, group 17, forage...... 18.0
Grass, forage, fodder and hay, group 17, hay......... 30.0
Guava................................................ 0.4
* * * * *
Jaboticaba........................................... 0.4
* * * * *
Mango................................................ 0.6
* * * * *
Onion, green, subgroup 3-07B......................... 5.0
Papaya............................................... 0.6
Passionfruit......................................... 0.4
* * * * *
Peanut............................................... 0.02
Peanut, hay.......................................... 55.0
Peanut, oil.......................................... 0.04
* * * * *
Sapodilla............................................ 0.6
Sapote, black........................................ 0.6
Sapote, mamey........................................ 0.6
* * * * *
Star apple........................................... 0.6
Starfruit............................................ 0.4
* * * * *
Vegetable, tuberous and corm, except potato, subgroup 0.02
1D..................................................
Wax jambu............................................ 0.4
------------------------------------------------------------------------
(b) Section 18 emergency exemptions. [Reserved]
(c) Tolerances with regional registrations. [Reserved]
(d) * * *
(1) * * *
------------------------------------------------------------------------
Expiration/
Commodity Parts per revocation
million date
------------------------------------------------------------------------
Vegetable, bulb, group 3-07................... 0.20 9/30/10
Vegetable, leaves of root and tuber, group 2.. 0.20 9/30/10
Vegetable, root and tuber, group 1............ 0.10 9/30/10
------------------------------------------------------------------------
(2) * * *
------------------------------------------------------------------------
Expiration/
Commodity Parts per revocation
million date
------------------------------------------------------------------------
Animal feed, non-grass, group 18.............. 10.0 9/30/10
Grain, cereal, forage, fodder and straw, group 10.0 9/30/10
16...........................................
Grass, forage, fodder and hay, group 17....... 10.0 9/30/10
Herb and spice, group 19...................... 10.0 9/30/10
Vegetable, foliage of legume, group 7......... 10.0 9/30/10
Vegetable, legume, group 6.................... 0.10 9/30/10
------------------------------------------------------------------------
[FR Doc. E8-4027 Filed 3-4-08; 8:45 am]
BILLING CODE 6560-50-S