Pyroxasulfone; Pesticide Tolerances, 54259-54264 [2018-23002]
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5. Amend Appendix C to Part 4 by
revising the entries for Agranulocytosis,
Anemia, Hodgkin’s lymphoma, and
■
Leukemia and adding in alphabetical
order, a new entry for Hematologic to
read as follows:.
Appendix C to Part 4—Alphabetical
Index of Disabilities
Diagnostic
code No.
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Agranulocytosis, acquired ....................................................................................................................................................................
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Anemia:
Acquired hemolytic anemia ..........................................................................................................................................................
Folic acid deficiency .....................................................................................................................................................................
Iron deficiency anemia .................................................................................................................................................................
Pernicious anemia and Vitamin B12 deficiency anemia ...............................................................................................................
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Hematologic:
Essential thrombocythemia and primary myelofibrosis ................................................................................................................
Immune thrombocytopenia ...........................................................................................................................................................
Multiple myeloma ..........................................................................................................................................................................
Myelodysplastic syndromes ..........................................................................................................................................................
Solitary plasmacytoma .................................................................................................................................................................
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Hodgkin’s lymphoma ...........................................................................................................................................................................
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Leukemia:
Chronic myelogenous leukemia (CML) (chronic myeloid leukemia or chronic granulocytic leukemia) .......................................
Leukemia ......................................................................................................................................................................................
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[FR Doc. 2018–23517 Filed 10–26–18; 8:45 am]
178 (see also Unit I.C. of the
BILLING CODE 8320–01–P
SUPPLEMENTARY INFORMATION).
40 CFR Part 180
[EPA–HQ–OPP–2017–0334; FRLc–9983–29]
Pyroxasulfone; Pesticide Tolerances
Environmental Protection
Agency (EPA).
ACTION: Final rule.
AGENCY:
This regulation establishes
tolerances for residues of pyroxasulfone
in or on multiple commodities which
are identified and discussed later in this
document. In addition, the established
pyroxasulfone tolerance on cotton,
undelinted seed is removed.
Interregional Research Project Number 4
(IR–4) requested these tolerances under
the Federal Food, Drug, and Cosmetic
Act (FFDCA).
DATES: This regulation is effective
October 29, 2018. Objections and
requests for hearings must be received
on or before December 28, 2018, and
must be filed in accordance with the
instructions provided in 40 CFR part
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SUMMARY:
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FOR FURTHER INFORMATION CONTACT:
Michael L. Goodis, Registration Division
(7505P), Office of Pesticide Programs,
Environmental Protection Agency, 1200
Pennsylvania Ave. NW, Washington, DC
20460–0001; main telephone number:
(703) 305–7090; email address:
RDFRNotices@epa.gov.
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A. Does this action apply to me?
The docket for this action,
identified by docket identification (ID)
number EPA–HQ–OPP–2017–0334, is
available at https://www.regulations.gov
or at the Office of Pesticide Programs
Regulatory Public Docket (OPP Docket)
in the Environmental Protection Agency
Docket Center (EPA/DC), West William
Jefferson Clinton Bldg., Rm. 3334, 1301
Constitution Ave. NW, Washington, DC
20460–0001. The Public Reading Room
is open from 8:30 a.m. to 4:30 p.m.,
Monday through Friday, excluding legal
holidays. The telephone number for the
Public Reading Room is (202) 566–1744,
and the telephone number for the OPP
Docket is (703) 305–5805. Please review
the visitor instructions and additional
information about the docket available
at https://www.epa.gov/dockets.
SUPPLEMENTARY INFORMATION:
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I. General Information
ADDRESSES:
ENVIRONMENTAL PROTECTION
AGENCY
*
7702
You may be potentially affected by
this action if you are an agricultural
producer, food manufacturer, or
pesticide manufacturer. The following
list of North American Industrial
Classification System (NAICS) codes is
not intended to be exhaustive, but rather
provides a guide to help readers
determine whether this document
applies to them. Potentially affected
entities may include:
• Crop production (NAICS code 111).
• Animal production (NAICS code
112).
• Food manufacturing (NAICS code
311).
• Pesticide manufacturing (NAICS
code 32532).
B. How can I get electronic access to
other related information?
You may access a frequently updated
electronic version of EPA’s tolerance
regulations at 40 CFR part 180 through
the Government Printing Office’s e-CFR
site at https://www.ecfr.gov/cgi-bin/textidx?&c=ecfr&tpl=/ecfrbrowse/Title40/
40tab_02.tpl.
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C. How can I file an objection or hearing
request?
Under FFDCA section 408(g), 21
U.S.C. 346a, any person may file an
objection to any aspect of this regulation
and may also request a hearing on those
objections. You must file your objection
or request a hearing on this regulation
in accordance with the instructions
provided in 40 CFR part 178. To ensure
proper receipt by EPA, you must
identify docket ID number EPA–HQ–
OPP–2017–0334 in the subject line on
the first page of your submission. All
objections and requests for a hearing
must be in writing, and must be
received by the Hearing Clerk on or
before December 28, 2018. Addresses for
mail and hand delivery of objections
and hearing requests are provided in 40
CFR 178.25(b).
In addition to filing an objection or
hearing request with the Hearing Clerk
as described in 40 CFR part 178, please
submit a copy of the filing (excluding
any Confidential Business Information
(CBI)) for inclusion in the public docket.
Information not marked confidential
pursuant to 40 CFR part 2 may be
disclosed publicly by EPA without prior
notice. Submit the non-CBI copy of your
objection or hearing request, identified
by docket ID number EPA–HQ–OPP–
2017–0334, by one of the following
methods:
• Federal eRulemaking Portal: https://
www.regulations.gov. Follow the online
instructions for submitting comments.
Do not submit electronically any
information you consider to be CBI or
other information whose disclosure is
restricted by statute.
• Mail: OPP Docket, Environmental
Protection Agency Docket Center (EPA/
DC), (28221T), 1200 Pennsylvania Ave.
NW, Washington, DC 20460–0001.
• Hand Delivery: To make special
arrangements for hand delivery or
delivery of boxed information, please
follow the instructions at https://
www.epa.gov/dockets/contacts.html.
Additional instructions on
commenting or visiting the docket,
along with more information about
dockets generally, is available at https://
www.epa.gov/dockets.
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II. Summary of Petitioned-For
Tolerance
In the Federal Register of October 23,
2017 (82 FR 49020) (FRL–9967–37),
EPA issued a document pursuant to
FFDCA section 408(d)(3), 21 U.S.C.
346a(d)(3), announcing the filing of a
pesticide petitions (PP 7E8570 &
7E8585) by IR–4 Headquarters, Rutgers,
The State University of New Jersey, 500
College Road East, Suite 201 W,
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Princeton, NJ 08540. The petitions
requested that 40 CFR 180.659 be
amended as follows:
a. Amend 180.659(a)(1), by
establishing a tolerance for residues of
the herbicide pyroxasulfone, including
its metabolites and degradates,
determined by measuring only the sum
of pyroxasulfone, 3-[[[5(difluoromethoxy)-1-methyl-3(trifluoromethyl)-1 H-pyrazol-4yl]methyl]sulfonyl]-4,5-dihydro-5,5dimethylisoxazole, and its metabolite, 5(difluoromethoxy)-1-methyl-3(trifluoromethyl)-1 H-pyrazol-4carboxylic acid (M-3), calculated as the
stoichiometric equivalent of
pyroxasulfone, in or on the commodity:
Cottonseed subgroup 20C at 0.04 parts
per million (ppm). In addition, the
petitioner requested removal of the
established tolerance on Cotton,
undelinted seed at 0.04 ppm (PP
7E8585).
b. Amend 180.659(a)(5) by
establishing a tolerance for residues of
the herbicide pyroxasulfone, including
its metabolites and degradates,
determined by measuring only the sum
of pyroxasulfone, (3-[(5difluoromethoxy-1-methyl-3(trifluoromethyl)pyrazol-4ylmethylsulfonyl]-4,5-dihydro-5,5dimethyl-1,2-oxazole), and its
metabolites, M-1 (5-difluoromethoxy-1methyl-3-trifluoromethyl-1H-pyrazol-4yl) methanesulfonic acid), M-3 (5difluoromethoxy-1-methyl-3trifluoromethyl-1H-pyrazol-4-carboxylic
acid), M-25 (5-difluoromethoxy-3trifluoromethyl-1H-pyrazol-4yl)methanesulfonic acid) and M-28 (3[1-carboxy-2-(5,5-dimethyl-4,5dihydroisoxazol-3-ylthio)ethylamino]-3oxopropanoic acid) calculated as the
stoichiometric equivalent of
pyroxasulfone, in or on the
commodities: Peppermint, oil at 0.48
ppm; peppermint, tops at 0.15 ppm;
spearmint, oil at 0.48 ppm; spearmint,
tops at 0.15 ppm; soybean, vegetable,
succulent at 0.2 ppm (PP 7E8570); and
Leaf petiole vegetable subgroup 22B at
0.3 ppm (PP 7E8585).
c. Amend 180.659(c) Tolerances with
regional registrations, by establishing a
tolerance for residues of the herbicide
pyroxasulfone, including its metabolites
and degradates, determined by
measuring only the sum of
pyroxasulfone, (3-[(5-difluoromethoxy1-methyl-3-(trifluoromethyl)pyrazol-4ylmethylsulfonyl]-4,5-dihydro-5,5dimethyl-1,2-oxazole), and its
metabolites, M-1 (5-difluoromethoxy-1methyl-3-trifluoromethyl-1H-pyrazol-4yl) methanesulfonic acid), M-3 (5difluoromethoxy-1-methyl-3trifluoromethyl-1H-pyrazol-4-carboxylic
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acid), M-25 (5-difluoromethoxy-3trifluoromethyl-1H-pyrazol-4yl)methanesulfonic acid) and M-28 (3[1-carboxy-2-(5,5-dimethyl-4,5dihydroisoxazol-3-ylthio)ethylamino]-3oxopropanoic acid) calculated as the
stoichiometric equivalent of
pyroxasulfone, in or on the
commodities: Grass, forage at 0.5 ppm
and grass, hay at 1.0 ppm (PP 7E8570).
These documents referenced a
summary of each petition prepared by
K–1 Chemical, USA Inc., the registrant,
that are available in the docket, https://
www.regulations.gov.
One comment was received on the
notice of filings. EPA’s response to the
comment is discussed in Unit IV.C.
Consistent with the authority in
FFDCA 408(d)(4)(A)(i), EPA is issuing
tolerances that vary from what the
petitioner sought. The reasons for these
changes are explained in Unit IV.D.
III. Aggregate Risk Assessment and
Determination of Safety
Section 408(b)(2)(A)(i) of FFDCA
allows EPA to establish a tolerance (the
legal limit for a pesticide chemical
residue in or on a food) only if EPA
determines that the tolerance is ‘‘safe.’’
Section 408(b)(2)(A)(ii) of FFDCA
defines ‘‘safe’’ to mean that ‘‘there is a
reasonable certainty that no harm will
result from aggregate exposure to the
pesticide chemical residue, including
all anticipated dietary exposures and all
other exposures for which there is
reliable information.’’ This includes
exposure through drinking water and in
residential settings but does not include
occupational exposure. Section
408(b)(2)(C) of FFDCA requires EPA to
give special consideration to exposure
of infants and children to the pesticide
chemical residue in establishing a
tolerance and to ‘‘ensure that there is a
reasonable certainty that no harm will
result to infants and children from
aggregate exposure to the pesticide
chemical residue. . . .’’
Consistent with FFDCA section
408(b)(2)(D), and the factors specified in
FFDCA section 408(b)(2)(D), EPA has
reviewed the available scientific data
and other relevant information in
support of this action. EPA has
sufficient data to assess the hazards of
and to make a determination on
aggregate exposure for pyroxasulfone
including exposure resulting from the
tolerances established by this action.
EPA’s assessment of exposures and risks
associated with pyroxasulfone follows.
A. Toxicological Profile
EPA has evaluated the available
toxicity data and considered their
validity, completeness, and reliability as
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well as the relationship of the results of
the studies to human risk. EPA has also
considered available information
concerning the variability of the
sensitivities of major identifiable
subgroups of consumers, including
infants and children.
The toxicology database for
pyroxasulfone is adequate for evaluating
and characterizing toxicity and selecting
endpoints for purposes of this risk
assessment. Pyroxasulfone acute
toxicity to mammals is low by all routes
of exposure. Subchronic and chronic
oral studies in mice, rats and dogs
produced a variety of effects including
cardiac toxicity (increased
cardiomyopathy), liver toxicity
(centrilobular hepatocellular
hypertrophy, histopathological and/or
clinical pathological indicators), kidney
toxicity (nephropathy), neurotoxicity
(impaired hind limb function, ataxia,
tremors, sciatic nerve lesions, axonal/
myelin degeneration in the sciatic nerve
and spinal cord sections), skeletal
muscle myopathy, urinary bladder
mucosal hyperplasia, and urinary
bladder transitional cell papillomas.
Dogs appear to be the most sensitive
species in regard to neurotoxic effects of
pyroxasulfone via the oral route.
Cardiac toxicity (myofiber degeneration
and local inflammation) were also seen
in a rat dermal toxicity study.
Pyroxasulfone did not elicit
immunotoxic effects in rats or mice.
Neurotoxicity was seen in a
developmental neurotoxicity study in
offspring rats (decreased brain weight,
decreased thickness of the
hippocampus, corpus callosum and
cerebellum). There is evidence of fetal
and offspring quantitative susceptibility
in the developmental neurotoxicity
study in rats as effects occurred in the
absence of maternal toxicity. There is no
concern for reproductive toxicity.
Pyroxasulfone is classified as ‘‘Not
Likely to be Carcinogenic to Humans’’ at
doses that do not cause crystals with
subsequent calculi formation resulting
in cellular damage of the urinary tract.
The Agency has determined that the
quantification of risk using a non-linear
approach (i.e., reference dose (RfD)) will
adequately account for all chronic
toxicity, including carcinogenicity, that
could result from exposure to
pyroxasulfone.
Specific information on the studies
received and the nature of the adverse
effects caused by pyroxasulfone as well
as the no-observed-adverse-effect-level
(NOAEL) and the lowest-observedadverse-effect-level (LOAEL) from the
toxicity studies can be found at https://
www.regulations.gov in document titled,
‘‘SUBJECT: Pyroxasulfone Human
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Health Risk Assessment for the Section
3 New Uses of Pyroxasulfone on Mint,
Edamame (vegetable soybean), Grass
(seed crop) for the Pacific Northwest
only, Leaf Petiole Vegetable Subgroup
22B and Expansion of Cottonseed
Subgroup 20C,’’ at pages 34–79 in
docket ID number EPA–HQ–OPP–2017–
0334.
B. Toxicological Points of Departure/
Levels of Concern
Once a pesticide’s toxicological
profile is determined, EPA identifies
toxicological points of departure (POD)
and levels of concern to use in
evaluating the risk posed by human
exposure to the pesticide. For hazards
that have a threshold below which there
is no appreciable risk, the toxicological
POD is used as the basis for derivation
of reference values for risk assessment.
PODs are developed based on a careful
analysis of the doses in each
toxicological study to determine the
dose at which no adverse effects are
observed (the NOAEL) and the lowest
dose at which adverse effects of concern
are identified (the LOAEL). Uncertainty/
safety factors are used in conjunction
with the POD to calculate a safe
exposure level—generally referred to as
a population-adjusted dose (PAD) or a
reference dose (RfD)—and a safe margin
of exposure (MOE). For non-threshold
risks, the Agency assumes that any
amount of exposure will lead to some
degree of risk. Thus, the Agency
estimates risk in terms of the probability
of an occurrence of the adverse effect
expected in a lifetime. For more
information on the general principles
EPA uses in risk characterization and a
complete description of the risk
assessment process, see https://
www2.epa.gov/pesticide-science-andassessing-pesticide-risks/assessinghuman-health-risk-pesticides.
A summary of the toxicological
endpoints for pyroxasulfone used for
human risk assessment is discussed in
Unit III of the final rule published in the
Federal Register of May 17, 2018 (83 FR
22854) (FRL–9977–25).
C. Exposure Assessment
1. Dietary exposure from food and
feed uses. In evaluating dietary
exposure to pyroxasulfone, EPA
considered exposure under the
petitioned-for tolerances as well as all
existing pyroxasulfone tolerances in 40
CFR 180.659. EPA assessed dietary
exposures from pyroxasulfone 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
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possibility of an effect of concern
occurring as a result of a 1-day or single
exposure.
Such effects were identified for
pyroxasulfone. In estimating acute
dietary exposure, EPA used 2003–2008
food consumption data from the United
States Department of Agriculture’s
(USDA) National Health and Nutrition
Survey/What We Eat in America
(NHANES/WWEIA). As to residue levels
in food, EPA assumed 100 percent crop
treated (PCT) and tolerance-level
residues adjusted for metabolites that
are not in the tolerance expression,
except for soybean and subgroup 22B
commodities, for which EPA used
anticipated residues from field trial
data.
ii. Chronic exposure. In conducting
the chronic dietary exposure assessment
EPA used the 2003–2008 food
consumption data from the USDA’s
NHANES/WWEIA. As to residue levels
in food, EPA assumed 100 PCT and
tolerance level residues that were
adjusted for metabolites not in the
tolerance expression, except for soybean
and subgroup 22B commodities, for
which EPA used anticipated residues
from field trial data.
iii. Cancer. Based on the data
summarized in Unit III.A., EPA has
concluded that a nonlinear RfD
approach is appropriate for assessing
cancer risk to pyroxasulfone. Cancer
risk was assessed using the same
exposure estimates as discussed in Unit
III.C.1.ii., chronic exposure.
iv. Anticipated residue and percent
crop treated (PCT) information. EPA did
not use PCT information in the dietary
assessment for pyroxasulfone; 100% CT
was assumed for all food commodities.
Tolerance-level residues were used for
all commodities except soybean and
subgroup 22B commodities, for which
EPA used anticipated residues from
field trial data.
Section 408(b)(2)(E) of FFDCA
authorizes EPA to use available data and
information on the anticipated residue
levels of pesticide residues in food and
the actual levels of pesticide residues
that have been measured in food. If EPA
relies on such information, EPA must
require pursuant to FFDCA section
408(f)(1) that data be provided 5 years
after the tolerance is established,
modified, or left in effect, demonstrating
that the levels in food are not above the
levels anticipated. For the present
action, EPA will issue such data call-ins
as are required by FFDCA section
408(b)(2)(E) and authorized under
FFDCA section 408(f)(1). Data will be
required to be submitted no later than
5 years from the date of issuance of
these tolerances.
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2. Dietary exposure from drinking
water. The Agency used screening level
water exposure models in the dietary
exposure analysis and risk assessment
for pyroxasulfone in drinking water.
These simulation models take into
account data on the physical, chemical,
and fate/transport characteristics of
pyroxasulfone. Further information
regarding EPA drinking water models
used in pesticide exposure assessment
can be found at https://www2.epa.gov/
pesticide-science-and-assessingpesticide-risks/about-water-exposuremodels-used-pesticide.
Based on the Pesticide Root Zone
Model/Exposure Analysis Modeling
System (PRZM/EXAMS) and Pesticide
Root Zone Model Ground Water (PRZM
GW), the estimated drinking water
concentrations (EDWCs) of
pyroxasulfone for acute exposures are
estimated to be 16.7 parts per billion
(ppb) for surface water and 210 ppb for
ground water. EDWCs of pyroxasulfone
for chronic exposures for non-cancer
assessments are estimated to be 4.5 ppb
for surface water and 174 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 210 ppb was
used to assess the contribution to
drinking water. For chronic dietary risk
assessment, the water concentration
value of 174 ppb was used to assess 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).
Pyroxasulfone is not registered for any
specific use patterns that would result
in residential exposure.
Further information regarding EPA
standard assumptions and generic
inputs for residential exposures may be
found at https://www2.epa.gov/pesticidescience-and-assessing-pesticide-risks/
standard-operating-proceduresresidential-pesticide.
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.’’
EPA has not found pyroxasulfone to
share a common mechanism of toxicity
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with any other substances, and
pyroxasulfone does not appear to
produce a toxic metabolite produced by
other substances. For the purposes of
this tolerance action, therefore, EPA has
assumed that pyroxasulfone does not
have a common 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 EPA’s website at EPA’s
website at https://www2.epa.gov/
pesticide-science-and-assessingpesticide-risks/cumulative-assessmentrisk-pesticides.
D. Safety Factor for Infants and
Children
1. In general. Section 408(b)(2)(C) of
FFDCA provides that EPA shall apply
an additional tenfold (10X) 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 referred to as the
FQPA Safety Factor (SF). In applying
this provision, EPA either retains the
default value of 10X, or uses a different
additional safety factor when reliable
data available to EPA support the choice
of a different factor.
2. Prenatal and postnatal sensitivity.
Pyroxasulfone did not exhibit
developmental toxicity in the rat
guideline study at the limit dose of
1,000 mg/kg/day and it exhibited slight
developmental toxicity in rabbits
(reduced fetal weight and resorptions) at
the limit dose of 1,000 mg/kg/day.
However, developmental effects
(decreased brain weight and
morphometric changes) were noted in
offspring at 300 mg/kg/day in the rat
developmental neurotoxicity (DNT)
study compared to no maternal toxicity
at 900 mg/kg/day. In a reproductive
toxicity in rats, reduced pup weight and
body weight gains during lactation
occurred at similar or higher doses
causing pronounced maternal toxicity
(reduced body weight, body weight gain
and food consumption and increased
kidney weight, cardiomyopathy and
urinary bladder mucosal hyperplasia
with inflammation).
3. Conclusion. EPA has determined
that reliable data show the safety of
infants and children would be
adequately protected if the FQPA SF
were reduced to 1x. That decision is
based on the following findings:
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i. The toxicity database for
pyroxasulfone is complete.
ii. The neurotoxicity database,
including acute, subchronic and chronic
studies, shows adverse effects from
pyroxasulfone exposure in mice, rats
and dogs, with the latter species
showing greatest sensitivity. Although
the DNT study indicated offspring are
more sensitive to neurotoxic effects of
pyroxasulfone, the dose-response is well
characterized for neurotoxicity and a
NOAEL is identified; therefore, there is
no residual uncertainty with regard to
neurotoxic effects for which a 10X must
be retained.
iii. As noted in Unit III.D.2., the
available database shows evidence of
increased susceptibility of fetuses and
offspring in a DNT study in rats and in
a developmental study in rabbits
following in utero or post-natal
exposure to pyroxasulfone. The Agency
concludes, however, that there is no
residual uncertainty concerning these
effects. The available studies show clear
NOAELs and LOAELs for these effects,
which are occurring only at doses much
higher than the endpoints on which the
Agency is regulating.
iv. There are no residual uncertainties
in the exposure databases. The dietary
food exposure assessments were
performed based on 100 PCT and
tolerance-level residues or residues
based on field trials. EPA made
conservative (protective) assumptions in
the ground and surface water modeling
used to assess exposure to
pyroxasulfone in drinking water. These
assessments will not underestimate the
exposure and risks posed by
pyroxasulfone.
E. Aggregate Risks and Determination of
Safety
EPA determines whether acute and
chronic dietary pesticide exposures are
safe by comparing aggregate exposure
estimates to the acute PAD (aPAD) and
chronic PAD (cPAD). For linear cancer
risks, EPA calculates the lifetime
probability of acquiring cancer given the
estimated aggregate exposure. Short-,
intermediate-, and chronic-term risks
are evaluated by comparing the
estimated aggregate food, water, and
residential exposure to the appropriate
PODs to ensure that an adequate MOE
exists.
1. Acute risk. Using the exposure
assumptions discussed in this unit for
acute exposure analysis, the risk
estimate for acute dietary exposure from
food and water to pyroxasulfone is at
3.7% of the aPAD for all infants less
than 1 year old, the population group
receiving the greatest exposure. The
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acute dietary risk is not of concern
(<100% aPAD).
2. Chronic risk. Using the exposure
assumptions described in this unit for
chronic exposure analysis, EPA has
concluded that risk estimates for
chronic exposure to pyroxasulfone from
food and water are not of concern
(<100% cPAD) with a risk estimate at
50% of the cPAD for all infants less than
1 year old, the population group
receiving the greatest exposure. There
are no residential uses for
pyroxasulfone.
3. Short-and intermediate term risk.
Short- and intermediate-term adverse
effects were identified; however,
pyroxasulfone is not registered for any
use patterns that would result in shortor intermediate-term residential
exposure. Short- and intermediate-term
risk is assessed based on short- and
intermediate-term residential exposure
plus chronic dietary exposure. Because
there is no short- or intermediate-term
residential exposure and chronic dietary
exposure has already been assessed
under the appropriately protective
cPAD (which is at least as protective as
the POD used to assess short-term risk),
no further assessment of short- or
intermediate-term risk is necessary, and
EPA relies on the chronic dietary risk
assessment for evaluating short- and
intermediate-term risk for
pyroxasulfone.
4. Aggregate cancer risk for U.S.
population. As explained in Unit III.A.,
the Agency has determined that the
quantification of risk using a non-linear
(i.e., RfD) approach will adequately
account for all chronic toxicity,
including carcinogenicity, that could
result from exposure to pyroxasulfone.
Therefore, based on the results of the
chronic risk assessment discussed in
Unit III.E.2., pyroxasulfone is not
expected to pose a cancer risk to
humans.
5. 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
pyroxasulfone residues.
IV. Other Considerations
amozie on DSK3GDR082PROD with RULES
A. Analytical Enforcement Methodology
Adequate enforcement methodology
(high performance liquid
chromatography/triple quadrupole mass
spectrometry (LC/MS/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;
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telephone number: (410) 305–2905;
email address: residuemethods@
epa.gov.
B. International Residue Limits
In making its tolerance decisions, EPA
seeks to harmonize U.S. tolerances with
international standards whenever
possible, consistent with U.S. food
safety standards and agricultural
practices. EPA considers the
international maximum residue limits
(MRLs) established by the Codex
Alimentarius Commission (Codex), as
required by FFDCA section 408(b)(4).
The Codex Alimentarius is a joint
United Nations Food and Agriculture
Organization/World Health
Organization food standards program,
and it is recognized as an international
food safety standards-setting
organization in trade agreements to
which the United States is a party. EPA
may establish a tolerance that is
different from a Codex MRL; however,
FFDCA section 408(b)(4) requires that
EPA explain the reasons for departing
from the Codex level.
The Codex has not established a MRL
for residues of pyroxasulfone in or on
any of the petitioned-for commodities
associated with this regulatory action.
C. Response to Comments
One anonymous public comment was
received that expressed concerns about
the cost of EPA regulations to tax payers
and corporations. This comment did not
raise any issue relevant to the Agency’s
safety determination for this tolerance
action. Section 408 of the Federal Food,
Drug and Cosmetic Act (FFDCA) allows
EPA to set tolerances for residues of
pesticide chemicals when it determines
that the tolerance meets the safety
standard imposed by that statute. EPA
has made that determination for the
pyroxasulfone tolerances established by
this final rule.
D. Revisions to Petitioned-For
Tolerances
EPA calculated tolerance levels using
the Organization for Economic
Cooperation and Development (OECD)
tolerance calculation procedures,
available field trial residue data, and
metabolite concentrations covered to
parent equivalents. The Agency is also
harmonizing with relevant Canadian
MRLs. In addition, the Agency is using
commodity terminology consistent with
the terms generally used for tolerances.
As a result, the Agency is establishing
tolerances that differ from the
petitioned-for tolerances as follows: (1)
The proposed pyroxasulfone tolerances
on both Peppermint, oil and Spearmint,
oil at 0.48 ppm are being established at
PO 00000
Frm 00035
Fmt 4700
Sfmt 4700
54263
0.70 ppm; (2) the proposed
pyroxasulfone tolerances on both
Peppermint, fresh leaves and Spearmint,
fresh leaves at 0.15 ppm are being each
established at 0.20 ppm; and (3) the
proposed tolerance on Leaf petiole
vegetable subgroup 22B at 0.3 ppm is
being established at 0.80 ppm.
In addition, although the petitioner
requested a tolerance on Soybean,
vegetable, succulent at 0.2 ppm, this
term is broad and covers two forms of
vegetable soybean—Soybean, vegetable,
succulent shelled, and Vegetable,
soybean, edible podded; therefore, to
conform to the Agency’s commodity
terminology for soybeans, the Agency is
establishing the tolerance requested as
separate tolerances at 0.40 ppm for both
forms of succulent soybean vegetable.
V. Conclusion
Therefore, tolerances are established
for residues of pyroxasulfone, including
its metabolites and degradates, in or on
Cottonseed subgroup 20C at 0.04 ppm;
Leaf petiole vegetable subgroup 22B at
0.80 ppm; Peppermint, fresh leaves at
0.20 ppm; Peppermint, oil at 0.70 ppm;
Soybean, vegetable, succulent shelled at
0.40 ppm; Spearmint, fresh leaves at
0.20 ppm; Spearmint, oil at 0.70 ppm;
and Vegetable, soybean, edible podded
at 0.40 ppm. In addition, tolerances
with regional registrations are
established in or on Grass, forage at 0.50
ppm and Grass, hay 1.0 ppm. Lastly, the
Agency is removing the existing
pyroxasulfone tolerance on Cotton,
undelinted seed that is superseded by
this final rule.
VI. Statutory and Executive Order
Reviews
This action establishes tolerances
under FFDCA section 408(d) in
response to a petition submitted to the
Agency. The Office of Management and
Budget (OMB) has exempted these types
of actions from review under Executive
Order 12866, entitled ‘‘Regulatory
Planning and Review’’ (58 FR 51735,
October 4, 1993). Because this action
has been exempted from review under
Executive Order 12866, this action is
not subject to Executive Order 13211,
entitled ‘‘Actions Concerning
Regulations That Significantly Affect
Energy Supply, Distribution, or Use’’ (66
FR 28355, May 22, 2001) or Executive
Order 13045, entitled ‘‘Protection of
Children from Environmental Health
Risks and Safety Risks’’ (62 FR 19885,
April 23, 1997); or Executive Order
13771, entitled ‘‘Reducing Regulations
and Controlling Regulatory Costs’’ (82
FR 9339, February 3, 2017). This action
does not contain any information
collections subject to OMB approval
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Federal Register / Vol. 83, No. 209 / Monday, October 29, 2018 / Rules and Regulations
under the Paperwork Reduction Act
(PRA) (44 U.S.C. 3501 et seq.), nor does
it require any special considerations
under Executive Order 12898, entitled
‘‘Federal Actions to Address
Environmental Justice in Minority
Populations and Low-Income
Populations’’ (59 FR 7629, February 16,
1994).
Since tolerances and exemptions that
are established on the basis of a petition
under FFDCA section 408(d), such as
the tolerance in this final rule, do not
require the issuance of a proposed rule,
the requirements of the Regulatory
Flexibility Act (RFA) (5 U.S.C. 601 et
seq.), do not apply.
This action directly regulates growers,
food processors, food handlers, and food
retailers, not States or tribes, nor does
this action alter the relationships or
distribution of power and
responsibilities established by Congress
in the preemption provisions of FFDCA
section 408(n)(4). As such, the Agency
has determined that this action will not
have a substantial direct effect on States
or tribal governments, on the
relationship between the national
government and the States or tribal
governments, or on the distribution of
power and responsibilities among the
various levels of government or between
the Federal Government and Indian
tribes. Thus, the Agency has determined
that Executive Order 13132, entitled
‘‘Federalism’’ (64 FR 43255, August 10,
1999) and Executive Order 13175,
entitled ‘‘Consultation and Coordination
with Indian Tribal Governments’’ (65 FR
67249, November 9, 2000) do not apply
to this action. In addition, this action
does not impose any enforceable duty or
contain any unfunded mandate as
described under Title II of the Unfunded
Mandates Reform Act (UMRA) (2 U.S.C.
1501 et seq.).
This action does not involve any
technical standards that would require
Agency consideration of voluntary
consensus standards pursuant to section
12(d) of the National Technology
Transfer and Advancement Act
(NTTAA) (15 U.S.C. 272 note).
amozie on DSK3GDR082PROD with RULES
VII. Congressional Review Act
Pursuant to the Congressional Review
Act (5 U.S.C. 801 et seq.), EPA will
submit a report containing this rule and
other required information to the U.S.
Senate, the U.S. House of
Representatives, and the Comptroller
General of the United States prior to
publication of the rule in the Federal
Register. This action is not a ‘‘major
rule’’ as defined by 5 U.S.C. 804(2).
VerDate Sep<11>2014
16:53 Oct 26, 2018
Jkt 247001
List of Subjects in 40 CFR Part 180
Environmental protection,
Administrative practice and procedure,
Agricultural commodities, Pesticides
and pests, Reporting and recordkeeping
requirements.
Dated: October 9, 2018.
Michael L. Goodis,
Director, Registration Division, Office of
Pesticide Programs.
Therefore, 40 CFR chapter I is
amended as follows:
PART 180—[AMENDED]
1. The authority citation for part 180
continues to read as follows:
■
Authority: 21 U.S.C. 321(q), 346a and 371.
2. In § 180.659:
a. In the table in paragraph (a)(1):
i. Remove the entry ‘‘Cotton,
undelinted seed’’;
■ ii. Add alphabetically the commodity,
’’Cottonseed subgroup 20C’’;
■ b. In the table in paragraph (a)(5), add
alphabetically the commodities, ‘‘Leaf
petiole vegetable subgroup 22B’’;
‘‘Peppermint, fresh leaves’’;
‘‘Peppermint, oil’’; ‘‘Soybean, vegetable,
succulent shelled’’; ‘‘Spearmint fresh
leaves’’; ‘‘Spearmint, oil’’; and
‘‘Vegetable, soybean, edible podded’’;
and
■ c. Revise paragraph (c).
The additions and revisions read as
follows:
■
■
■
§ 180.659 Pyroxasulfone; tolerances for
residues.
(a) * * *
(1) * * *
*
*
*
*
*
(c) Tolerance with regional
registrations. Tolerances are established
for residues of the herbicide
pyroxasulfone, including its metabolites
and degradates, in or on the
commodities in the table below.
Compliance with the tolerance levels
specified below is to be determined by
measuring only the sum of
pyroxasulfone (3-[(5-difluoromethoxy-1methyl-3-(trifluoromethyl)pyrazol-4ylmethylsulfonyl]-4,5-dihydro-5,5dimethyl-1,2-oxazole), and its
metabolites, M–1 (5-difluoromethoxy-1methyl-3-trifluoromethyl-1H-pyrazol-4yl)methanesulfonic acid), M–3 (5difluoromethoxy-1-methyl-3trifluoromethyl-1H-pyrazol-4-carboxylic
acid), M–25 (5-difluoromethoxy-3trifluoromethyl-1H-pyrazol-4yl)methanesulfonic acid) and M–28 (3[1-carboxy-2-(5,5-dimethyl-4,5dihydroisoxazol-3-ylthio)ethylamino]-3oxopropanoic acid) calculated as the
stoichiometric equivalent of
pyroxasulfone, in or on the commodity.
Parts per
million
Commodity
Grass, forage ...........................................
Grass, hay ...............................................
*
*
*
*
0.50
1.0
*
[FR Doc. 2018–23002 Filed 10–26–18; 8:45 am]
BILLING CODE 6560–50–P
DEPARTMENT OF COMMERCE
National Oceanic and Atmospheric
Administration
Parts per
million
Commodity
50 CFR Part 648
[Docket No. 170828822–70999–04]
*
*
*
*
Cottonseed, subgroup 20C .....................
*
*
*
*
*
(5) * * *
*
*
*
*
0.04
*
*
*
*
*
*
Peppermint, fresh leaves ........................
Peppermint, oil ........................................
*
*
*
*
*
Soybean, vegetable, succulent shelled ...
Spearmint, fresh leaves ..........................
Spearmint, oil ..........................................
*
*
*
*
*
Vegetable, soybean, edible podded ........
*
Frm 00036
National Marine Fisheries
Service (NMFS), National Oceanic and
Atmospheric Administration (NOAA),
Commerce.
ACTION: Temporary rule; quota transfer.
AGENCY:
Parts per
million
*
*
*
*
Leaf petiole vegetable subgroup 22B .....
PO 00000
Fisheries of the Northeastern United
States; Summer Flounder Fishery;
Quota Transfer
*
Commodity
*
RIN 0648–XG574
*
Fmt 4700
*
*
Sfmt 4700
0.80
0.20
0.70
0.40
0.20
0.70
0.40
*
NMFS announces that the
State of North Carolina is transferring a
portion of its 2018 commercial summer
flounder quota to the State of New York.
This quota adjustment is necessary to
comply with the Summer Flounder,
Scup, and Black Sea Bass Fishery
Management Plan quota transfer
provisions. This announcement informs
the public of the revised commercial
quotas for North Carolina and New
York.
SUMMARY:
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[Federal Register Volume 83, Number 209 (Monday, October 29, 2018)]
[Rules and Regulations]
[Pages 54259-54264]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2018-23002]
=======================================================================
-----------------------------------------------------------------------
ENVIRONMENTAL PROTECTION AGENCY
40 CFR Part 180
[EPA-HQ-OPP-2017-0334; FRLc-9983-29]
Pyroxasulfone; Pesticide Tolerances
AGENCY: Environmental Protection Agency (EPA).
ACTION: Final rule.
-----------------------------------------------------------------------
SUMMARY: This regulation establishes tolerances for residues of
pyroxasulfone in or on multiple commodities which are identified and
discussed later in this document. In addition, the established
pyroxasulfone tolerance on cotton, undelinted seed is removed.
Interregional Research Project Number 4 (IR-4) requested these
tolerances under the Federal Food, Drug, and Cosmetic Act (FFDCA).
DATES: This regulation is effective October 29, 2018. Objections and
requests for hearings must be received on or before December 28, 2018,
and must be filed in accordance with the instructions provided in 40
CFR part 178 (see also Unit I.C. of the SUPPLEMENTARY INFORMATION).
ADDRESSES: The docket for this action, identified by docket
identification (ID) number EPA-HQ-OPP-2017-0334, is available at https://www.regulations.gov or at the Office of Pesticide Programs Regulatory
Public Docket (OPP Docket) in the Environmental Protection Agency
Docket Center (EPA/DC), West William Jefferson Clinton Bldg., Rm. 3334,
1301 Constitution Ave. NW, Washington, DC 20460-0001. The Public
Reading Room is open from 8:30 a.m. to 4:30 p.m., Monday through
Friday, excluding legal holidays. The telephone number for the Public
Reading Room is (202) 566-1744, and the telephone number for the OPP
Docket is (703) 305-5805. Please review the visitor instructions and
additional information about the docket available at https://www.epa.gov/dockets.
FOR FURTHER INFORMATION CONTACT: Michael L. Goodis, Registration
Division (7505P), Office of Pesticide Programs, Environmental
Protection Agency, 1200 Pennsylvania Ave. NW, Washington, DC 20460-
0001; main telephone number: (703) 305-7090; email address:
[email protected].
SUPPLEMENTARY INFORMATION:
I. General Information
A. Does this action apply to me?
You may be potentially affected by this action if you are an
agricultural producer, food manufacturer, or pesticide manufacturer.
The following list of North American Industrial Classification System
(NAICS) codes is not intended to be exhaustive, but rather provides a
guide to help readers determine whether this document applies to them.
Potentially affected entities may include:
Crop production (NAICS code 111).
Animal production (NAICS code 112).
Food manufacturing (NAICS code 311).
Pesticide manufacturing (NAICS code 32532).
B. How can I get electronic access to other related information?
You may access a frequently updated electronic version of EPA's
tolerance regulations at 40 CFR part 180 through the Government
Printing Office's e-CFR site at https://www.ecfr.gov/cgi-bin/text-idx?&c=ecfr&tpl=/ecfrbrowse/Title40/40tab_02.tpl.
[[Page 54260]]
C. How can I file an objection or hearing request?
Under FFDCA section 408(g), 21 U.S.C. 346a, any person may file an
objection to any aspect of this regulation and may also request a
hearing on those objections. You must file your objection or request a
hearing on this regulation in accordance with the instructions provided
in 40 CFR part 178. To ensure proper receipt by EPA, you must identify
docket ID number EPA-HQ-OPP-2017-0334 in the subject line on the first
page of your submission. All objections and requests for a hearing must
be in writing, and must be received by the Hearing Clerk on or before
December 28, 2018. Addresses for mail and hand delivery of objections
and hearing requests are provided in 40 CFR 178.25(b).
In addition to filing an objection or hearing request with the
Hearing Clerk as described in 40 CFR part 178, please submit a copy of
the filing (excluding any Confidential Business Information (CBI)) for
inclusion in the public docket. Information not marked confidential
pursuant to 40 CFR part 2 may be disclosed publicly by EPA without
prior notice. Submit the non-CBI copy of your objection or hearing
request, identified by docket ID number EPA-HQ-OPP-2017-0334, by one of
the following methods:
Federal eRulemaking Portal: https://www.regulations.gov.
Follow the online instructions for submitting comments. Do not submit
electronically any information you consider to be CBI or other
information whose disclosure is restricted by statute.
Mail: OPP Docket, Environmental Protection Agency Docket
Center (EPA/DC), (28221T), 1200 Pennsylvania Ave. NW, Washington, DC
20460-0001.
Hand Delivery: To make special arrangements for hand
delivery or delivery of boxed information, please follow the
instructions at https://www.epa.gov/dockets/contacts.html.
Additional instructions on commenting or visiting the docket, along
with more information about dockets generally, is available at https://www.epa.gov/dockets.
II. Summary of Petitioned-For Tolerance
In the Federal Register of October 23, 2017 (82 FR 49020) (FRL-
9967-37), EPA issued a document pursuant to FFDCA section 408(d)(3), 21
U.S.C. 346a(d)(3), announcing the filing of a pesticide petitions (PP
7E8570 & 7E8585) by IR-4 Headquarters, Rutgers, The State University of
New Jersey, 500 College Road East, Suite 201 W, Princeton, NJ 08540.
The petitions requested that 40 CFR 180.659 be amended as follows:
a. Amend 180.659(a)(1), by establishing a tolerance for residues of
the herbicide pyroxasulfone, including its metabolites and degradates,
determined by measuring only the sum of pyroxasulfone, 3-[[[5-
(difluoromethoxy)-1-methyl-3-(trifluoromethyl)-1 H-pyrazol-4-
yl]methyl]sulfonyl]-4,5-dihydro-5,5-dimethylisoxazole, and its
metabolite, 5-(difluoromethoxy)-1-methyl-3-(trifluoromethyl)-1 H-
pyrazol-4-carboxylic acid (M-3), calculated as the stoichiometric
equivalent of pyroxasulfone, in or on the commodity: Cottonseed
subgroup 20C at 0.04 parts per million (ppm). In addition, the
petitioner requested removal of the established tolerance on Cotton,
undelinted seed at 0.04 ppm (PP 7E8585).
b. Amend 180.659(a)(5) by establishing a tolerance for residues of
the herbicide pyroxasulfone, including its metabolites and degradates,
determined by measuring only the sum of pyroxasulfone, (3-[(5-
difluoromethoxy-1-methyl-3-(trifluoromethyl)pyrazol-4-
ylmethylsulfonyl]-4,5-dihydro-5,5-dimethyl-1,2-oxazole), and its
metabolites, M-1 (5-difluoromethoxy-1-methyl-3-trifluoromethyl-1H-
pyrazol-4-yl) methanesulfonic acid), M-3 (5-difluoromethoxy-1-methyl-3-
trifluoromethyl-1H-pyrazol-4-carboxylic acid), M-25 (5-difluoromethoxy-
3-trifluoromethyl-1H-pyrazol-4-yl)methanesulfonic acid) and M-28 (3-[1-
carboxy-2-(5,5-dimethyl-4,5-dihydroisoxazol-3-ylthio)ethylamino]-3-
oxopropanoic acid) calculated as the stoichiometric equivalent of
pyroxasulfone, in or on the commodities: Peppermint, oil at 0.48 ppm;
peppermint, tops at 0.15 ppm; spearmint, oil at 0.48 ppm; spearmint,
tops at 0.15 ppm; soybean, vegetable, succulent at 0.2 ppm (PP 7E8570);
and Leaf petiole vegetable subgroup 22B at 0.3 ppm (PP 7E8585).
c. Amend 180.659(c) Tolerances with regional registrations, by
establishing a tolerance for residues of the herbicide pyroxasulfone,
including its metabolites and degradates, determined by measuring only
the sum of pyroxasulfone, (3-[(5-difluoromethoxy-1-methyl-3-
(trifluoromethyl)pyrazol-4-ylmethylsulfonyl]-4,5-dihydro-5,5-dimethyl-
1,2-oxazole), and its metabolites, M-1 (5-difluoromethoxy-1-methyl-3-
trifluoromethyl-1H-pyrazol-4-yl) methanesulfonic acid), M-3 (5-
difluoromethoxy-1-methyl-3-trifluoromethyl-1H-pyrazol-4-carboxylic
acid), M-25 (5-difluoromethoxy-3-trifluoromethyl-1H-pyrazol-4-
yl)methanesulfonic acid) and M-28 (3-[1-carboxy-2-(5,5-dimethyl-4,5-
dihydroisoxazol-3-ylthio)ethylamino]-3-oxopropanoic acid) calculated as
the stoichiometric equivalent of pyroxasulfone, in or on the
commodities: Grass, forage at 0.5 ppm and grass, hay at 1.0 ppm (PP
7E8570).
These documents referenced a summary of each petition prepared by
K-1 Chemical, USA Inc., the registrant, that are available in the
docket, https://www.regulations.gov.
One comment was received on the notice of filings. EPA's response
to the comment is discussed in Unit IV.C.
Consistent with the authority in FFDCA 408(d)(4)(A)(i), EPA is
issuing tolerances that vary from what the petitioner sought. The
reasons for these changes are explained in Unit IV.D.
III. Aggregate Risk Assessment and Determination of Safety
Section 408(b)(2)(A)(i) of FFDCA allows EPA to establish a
tolerance (the legal limit for a pesticide chemical residue in or on a
food) only if EPA determines that the tolerance is ``safe.'' Section
408(b)(2)(A)(ii) of FFDCA defines ``safe'' to mean that ``there is a
reasonable certainty that no harm will result from aggregate exposure
to the pesticide chemical residue, including all anticipated dietary
exposures and all other exposures for which there is reliable
information.'' This includes exposure through drinking water and in
residential settings but does not include occupational exposure.
Section 408(b)(2)(C) of FFDCA requires EPA to give special
consideration to exposure of infants and children to the pesticide
chemical residue in establishing a tolerance and to ``ensure that there
is a reasonable certainty that no harm will result to infants and
children from aggregate exposure to the pesticide chemical residue. . .
.''
Consistent with FFDCA section 408(b)(2)(D), and the factors
specified in FFDCA section 408(b)(2)(D), EPA has reviewed the available
scientific data and other relevant information in support of this
action. EPA has sufficient data to assess the hazards of and to make a
determination on aggregate exposure for pyroxasulfone including
exposure resulting from the tolerances established by this action.
EPA's assessment of exposures and risks associated with pyroxasulfone
follows.
A. Toxicological Profile
EPA has evaluated the available toxicity data and considered their
validity, completeness, and reliability as
[[Page 54261]]
well as the relationship of the results of the studies to human risk.
EPA has also considered available information concerning the
variability of the sensitivities of major identifiable subgroups of
consumers, including infants and children.
The toxicology database for pyroxasulfone is adequate for
evaluating and characterizing toxicity and selecting endpoints for
purposes of this risk assessment. Pyroxasulfone acute toxicity to
mammals is low by all routes of exposure. Subchronic and chronic oral
studies in mice, rats and dogs produced a variety of effects including
cardiac toxicity (increased cardiomyopathy), liver toxicity
(centrilobular hepatocellular hypertrophy, histopathological and/or
clinical pathological indicators), kidney toxicity (nephropathy),
neurotoxicity (impaired hind limb function, ataxia, tremors, sciatic
nerve lesions, axonal/myelin degeneration in the sciatic nerve and
spinal cord sections), skeletal muscle myopathy, urinary bladder
mucosal hyperplasia, and urinary bladder transitional cell papillomas.
Dogs appear to be the most sensitive species in regard to neurotoxic
effects of pyroxasulfone via the oral route. Cardiac toxicity (myofiber
degeneration and local inflammation) were also seen in a rat dermal
toxicity study. Pyroxasulfone did not elicit immunotoxic effects in
rats or mice. Neurotoxicity was seen in a developmental neurotoxicity
study in offspring rats (decreased brain weight, decreased thickness of
the hippocampus, corpus callosum and cerebellum). There is evidence of
fetal and offspring quantitative susceptibility in the developmental
neurotoxicity study in rats as effects occurred in the absence of
maternal toxicity. There is no concern for reproductive toxicity.
Pyroxasulfone is classified as ``Not Likely to be Carcinogenic to
Humans'' at doses that do not cause crystals with subsequent calculi
formation resulting in cellular damage of the urinary tract. The Agency
has determined that the quantification of risk using a non-linear
approach (i.e., reference dose (RfD)) will adequately account for all
chronic toxicity, including carcinogenicity, that could result from
exposure to pyroxasulfone.
Specific information on the studies received and the nature of the
adverse effects caused by pyroxasulfone 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 in document titled, ``SUBJECT: Pyroxasulfone Human
Health Risk Assessment for the Section 3 New Uses of Pyroxasulfone on
Mint, Edamame (vegetable soybean), Grass (seed crop) for the Pacific
Northwest only, Leaf Petiole Vegetable Subgroup 22B and Expansion of
Cottonseed Subgroup 20C,'' at pages 34-79 in docket ID number EPA-HQ-
OPP-2017-0334.
B. Toxicological Points of Departure/Levels of Concern
Once a pesticide's toxicological profile is determined, EPA
identifies toxicological points of departure (POD) and levels of
concern to use in evaluating the risk posed by human exposure to the
pesticide. For hazards that have a threshold below which there is no
appreciable risk, the toxicological POD is used as the basis for
derivation of reference values for risk assessment. PODs are developed
based on a careful analysis of the doses in each toxicological study to
determine the dose at which no adverse effects are observed (the NOAEL)
and the lowest dose at which adverse effects of concern are identified
(the LOAEL). Uncertainty/safety factors are used in conjunction with
the POD to calculate a safe exposure level--generally referred to as a
population-adjusted dose (PAD) or a reference dose (RfD)--and a safe
margin of exposure (MOE). For non-threshold risks, the Agency assumes
that any amount of exposure will lead to some degree of risk. Thus, the
Agency estimates risk in terms of the probability of an occurrence of
the adverse effect expected in a lifetime. For more information on the
general principles EPA uses in risk characterization and a complete
description of the risk assessment process, see https://www2.epa.gov/pesticide-science-and-assessing-pesticide-risks/assessing-human-health-risk-pesticides.
A summary of the toxicological endpoints for pyroxasulfone used for
human risk assessment is discussed in Unit III of the final rule
published in the Federal Register of May 17, 2018 (83 FR 22854) (FRL-
9977-25).
C. Exposure Assessment
1. Dietary exposure from food and feed uses. In evaluating dietary
exposure to pyroxasulfone, EPA considered exposure under the
petitioned-for tolerances as well as all existing pyroxasulfone
tolerances in 40 CFR 180.659. EPA assessed dietary exposures from
pyroxasulfone 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.
Such effects were identified for pyroxasulfone. In estimating acute
dietary exposure, EPA used 2003-2008 food consumption data from the
United States Department of Agriculture's (USDA) National Health and
Nutrition Survey/What We Eat in America (NHANES/WWEIA). As to residue
levels in food, EPA assumed 100 percent crop treated (PCT) and
tolerance-level residues adjusted for metabolites that are not in the
tolerance expression, except for soybean and subgroup 22B commodities,
for which EPA used anticipated residues from field trial data.
ii. Chronic exposure. In conducting the chronic dietary exposure
assessment EPA used the 2003-2008 food consumption data from the USDA's
NHANES/WWEIA. As to residue levels in food, EPA assumed 100 PCT and
tolerance level residues that were adjusted for metabolites not in the
tolerance expression, except for soybean and subgroup 22B commodities,
for which EPA used anticipated residues from field trial data.
iii. Cancer. Based on the data summarized in Unit III.A., EPA has
concluded that a nonlinear RfD approach is appropriate for assessing
cancer risk to pyroxasulfone. Cancer risk was assessed using the same
exposure estimates as discussed in Unit III.C.1.ii., chronic exposure.
iv. Anticipated residue and percent crop treated (PCT) information.
EPA did not use PCT information in the dietary assessment for
pyroxasulfone; 100% CT was assumed for all food commodities. Tolerance-
level residues were used for all commodities except soybean and
subgroup 22B commodities, for which EPA used anticipated residues from
field trial data.
Section 408(b)(2)(E) of FFDCA authorizes EPA to use available data
and information on the anticipated residue levels of pesticide residues
in food and the actual levels of pesticide residues that have been
measured in food. If EPA relies on such information, EPA must require
pursuant to FFDCA section 408(f)(1) that data be provided 5 years after
the tolerance is established, modified, or left in effect,
demonstrating that the levels in food are not above the levels
anticipated. For the present action, EPA will issue such data call-ins
as are required by FFDCA section 408(b)(2)(E) and authorized under
FFDCA section 408(f)(1). Data will be required to be submitted no later
than 5 years from the date of issuance of these tolerances.
[[Page 54262]]
2. Dietary exposure from drinking water. The Agency used screening
level water exposure models in the dietary exposure analysis and risk
assessment for pyroxasulfone in drinking water. These simulation models
take into account data on the physical, chemical, and fate/transport
characteristics of pyroxasulfone. Further information regarding EPA
drinking water models used in pesticide exposure assessment can be
found at https://www2.epa.gov/pesticide-science-and-assessing-pesticide-risks/about-water-exposure-models-used-pesticide.
Based on the Pesticide Root Zone Model/Exposure Analysis Modeling
System (PRZM/EXAMS) and Pesticide Root Zone Model Ground Water (PRZM
GW), the estimated drinking water concentrations (EDWCs) of
pyroxasulfone for acute exposures are estimated to be 16.7 parts per
billion (ppb) for surface water and 210 ppb for ground water. EDWCs of
pyroxasulfone for chronic exposures for non-cancer assessments are
estimated to be 4.5 ppb for surface water and 174 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 210 ppb was used to assess
the contribution to drinking water. For chronic dietary risk
assessment, the water concentration value of 174 ppb was used to assess
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).
Pyroxasulfone is not registered for any specific use patterns that
would result in residential exposure.
Further information regarding EPA standard assumptions and generic
inputs for residential exposures may be found at https://www2.epa.gov/pesticide-science-and-assessing-pesticide-risks/standard-operating-procedures-residential-pesticide.
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.''
EPA has not found pyroxasulfone to share a common mechanism of
toxicity with any other substances, and pyroxasulfone does not appear
to produce a toxic metabolite produced by other substances. For the
purposes of this tolerance action, therefore, EPA has assumed that
pyroxasulfone does not have a common 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 EPA's website at EPA's
website at https://www2.epa.gov/pesticide-science-and-assessing-pesticide-risks/cumulative-assessment-risk-pesticides.
D. Safety Factor for Infants and Children
1. In general. Section 408(b)(2)(C) of FFDCA provides that EPA
shall apply an additional tenfold (10X) 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 referred to as the FQPA Safety
Factor (SF). In applying this provision, EPA either retains the default
value of 10X, or uses a different additional safety factor when
reliable data available to EPA support the choice of a different
factor.
2. Prenatal and postnatal sensitivity. Pyroxasulfone did not
exhibit developmental toxicity in the rat guideline study at the limit
dose of 1,000 mg/kg/day and it exhibited slight developmental toxicity
in rabbits (reduced fetal weight and resorptions) at the limit dose of
1,000 mg/kg/day. However, developmental effects (decreased brain weight
and morphometric changes) were noted in offspring at 300 mg/kg/day in
the rat developmental neurotoxicity (DNT) study compared to no maternal
toxicity at 900 mg/kg/day. In a reproductive toxicity in rats, reduced
pup weight and body weight gains during lactation occurred at similar
or higher doses causing pronounced maternal toxicity (reduced body
weight, body weight gain and food consumption and increased kidney
weight, cardiomyopathy and urinary bladder mucosal hyperplasia with
inflammation).
3. Conclusion. EPA has determined that reliable data show the
safety of infants and children would be adequately protected if the
FQPA SF were reduced to 1x. That decision is based on the following
findings:
i. The toxicity database for pyroxasulfone is complete.
ii. The neurotoxicity database, including acute, subchronic and
chronic studies, shows adverse effects from pyroxasulfone exposure in
mice, rats and dogs, with the latter species showing greatest
sensitivity. Although the DNT study indicated offspring are more
sensitive to neurotoxic effects of pyroxasulfone, the dose-response is
well characterized for neurotoxicity and a NOAEL is identified;
therefore, there is no residual uncertainty with regard to neurotoxic
effects for which a 10X must be retained.
iii. As noted in Unit III.D.2., the available database shows
evidence of increased susceptibility of fetuses and offspring in a DNT
study in rats and in a developmental study in rabbits following in
utero or post-natal exposure to pyroxasulfone. The Agency concludes,
however, that there is no residual uncertainty concerning these
effects. The available studies show clear NOAELs and LOAELs for these
effects, which are occurring only at doses much higher than the
endpoints on which the Agency is regulating.
iv. There are no residual uncertainties in the exposure databases.
The dietary food exposure assessments were performed based on 100 PCT
and tolerance-level residues or residues based on field trials. EPA
made conservative (protective) assumptions in the ground and surface
water modeling used to assess exposure to pyroxasulfone in drinking
water. These assessments will not underestimate the exposure and risks
posed by pyroxasulfone.
E. Aggregate Risks and Determination of Safety
EPA determines whether acute and chronic dietary pesticide
exposures are safe by comparing aggregate exposure estimates to the
acute PAD (aPAD) and chronic PAD (cPAD). For linear cancer risks, EPA
calculates the lifetime probability of acquiring cancer given the
estimated aggregate exposure. Short-, intermediate-, and chronic-term
risks are evaluated by comparing the estimated aggregate food, water,
and residential exposure to the appropriate PODs to ensure that an
adequate MOE exists.
1. Acute risk. Using the exposure assumptions discussed in this
unit for acute exposure analysis, the risk estimate for acute dietary
exposure from food and water to pyroxasulfone is at 3.7% of the aPAD
for all infants less than 1 year old, the population group receiving
the greatest exposure. The
[[Page 54263]]
acute dietary risk is not of concern (<100% aPAD).
2. Chronic risk. Using the exposure assumptions described in this
unit for chronic exposure analysis, EPA has concluded that risk
estimates for chronic exposure to pyroxasulfone from food and water are
not of concern (<100% cPAD) with a risk estimate at 50% of the cPAD for
all infants less than 1 year old, the population group receiving the
greatest exposure. There are no residential uses for pyroxasulfone.
3. Short-and intermediate term risk. Short- and intermediate-term
adverse effects were identified; however, pyroxasulfone is not
registered for any use patterns that would result in short- or
intermediate-term residential exposure. Short- and intermediate-term
risk is assessed based on short- and intermediate-term residential
exposure plus chronic dietary exposure. Because there is no short- or
intermediate-term residential exposure and chronic dietary exposure has
already been assessed under the appropriately protective cPAD (which is
at least as protective as the POD used to assess short-term risk), no
further assessment of short- or intermediate-term risk is necessary,
and EPA relies on the chronic dietary risk assessment for evaluating
short- and intermediate-term risk for pyroxasulfone.
4. Aggregate cancer risk for U.S. population. As explained in Unit
III.A., the Agency has determined that the quantification of risk using
a non-linear (i.e., RfD) approach will adequately account for all
chronic toxicity, including carcinogenicity, that could result from
exposure to pyroxasulfone. Therefore, based on the results of the
chronic risk assessment discussed in Unit III.E.2., pyroxasulfone is
not expected to pose a cancer risk to humans.
5. 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 pyroxasulfone residues.
IV. Other Considerations
A. Analytical Enforcement Methodology
Adequate enforcement methodology (high performance liquid
chromatography/triple quadrupole mass spectrometry (LC/MS/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; email address:
[email protected].
B. International Residue Limits
In making its tolerance decisions, EPA seeks to harmonize U.S.
tolerances with international standards whenever possible, consistent
with U.S. food safety standards and agricultural practices. EPA
considers the international maximum residue limits (MRLs) established
by the Codex Alimentarius Commission (Codex), as required by FFDCA
section 408(b)(4). The Codex Alimentarius is a joint United Nations
Food and Agriculture Organization/World Health Organization food
standards program, and it is recognized as an international food safety
standards-setting organization in trade agreements to which the United
States is a party. EPA may establish a tolerance that is different from
a Codex MRL; however, FFDCA section 408(b)(4) requires that EPA explain
the reasons for departing from the Codex level.
The Codex has not established a MRL for residues of pyroxasulfone
in or on any of the petitioned-for commodities associated with this
regulatory action.
C. Response to Comments
One anonymous public comment was received that expressed concerns
about the cost of EPA regulations to tax payers and corporations. This
comment did not raise any issue relevant to the Agency's safety
determination for this tolerance action. Section 408 of the Federal
Food, Drug and Cosmetic Act (FFDCA) allows EPA to set tolerances for
residues of pesticide chemicals when it determines that the tolerance
meets the safety standard imposed by that statute. EPA has made that
determination for the pyroxasulfone tolerances established by this
final rule.
D. Revisions to Petitioned-For Tolerances
EPA calculated tolerance levels using the Organization for Economic
Cooperation and Development (OECD) tolerance calculation procedures,
available field trial residue data, and metabolite concentrations
covered to parent equivalents. The Agency is also harmonizing with
relevant Canadian MRLs. In addition, the Agency is using commodity
terminology consistent with the terms generally used for tolerances.
As a result, the Agency is establishing tolerances that differ from
the petitioned-for tolerances as follows: (1) The proposed
pyroxasulfone tolerances on both Peppermint, oil and Spearmint, oil at
0.48 ppm are being established at 0.70 ppm; (2) the proposed
pyroxasulfone tolerances on both Peppermint, fresh leaves and
Spearmint, fresh leaves at 0.15 ppm are being each established at 0.20
ppm; and (3) the proposed tolerance on Leaf petiole vegetable subgroup
22B at 0.3 ppm is being established at 0.80 ppm.
In addition, although the petitioner requested a tolerance on
Soybean, vegetable, succulent at 0.2 ppm, this term is broad and covers
two forms of vegetable soybean--Soybean, vegetable, succulent shelled,
and Vegetable, soybean, edible podded; therefore, to conform to the
Agency's commodity terminology for soybeans, the Agency is establishing
the tolerance requested as separate tolerances at 0.40 ppm for both
forms of succulent soybean vegetable.
V. Conclusion
Therefore, tolerances are established for residues of
pyroxasulfone, including its metabolites and degradates, in or on
Cottonseed subgroup 20C at 0.04 ppm; Leaf petiole vegetable subgroup
22B at 0.80 ppm; Peppermint, fresh leaves at 0.20 ppm; Peppermint, oil
at 0.70 ppm; Soybean, vegetable, succulent shelled at 0.40 ppm;
Spearmint, fresh leaves at 0.20 ppm; Spearmint, oil at 0.70 ppm; and
Vegetable, soybean, edible podded at 0.40 ppm. In addition, tolerances
with regional registrations are established in or on Grass, forage at
0.50 ppm and Grass, hay 1.0 ppm. Lastly, the Agency is removing the
existing pyroxasulfone tolerance on Cotton, undelinted seed that is
superseded by this final rule.
VI. Statutory and Executive Order Reviews
This action establishes tolerances under FFDCA section 408(d) in
response to a petition submitted to the Agency. The Office of
Management and Budget (OMB) has exempted these types of actions from
review under Executive Order 12866, entitled ``Regulatory Planning and
Review'' (58 FR 51735, October 4, 1993). Because this action has been
exempted from review under Executive Order 12866, this action is not
subject to Executive Order 13211, entitled ``Actions Concerning
Regulations That Significantly Affect Energy Supply, Distribution, or
Use'' (66 FR 28355, May 22, 2001) or Executive Order 13045, entitled
``Protection of Children from Environmental Health Risks and Safety
Risks'' (62 FR 19885, April 23, 1997); or Executive Order 13771,
entitled ``Reducing Regulations and Controlling Regulatory Costs'' (82
FR 9339, February 3, 2017). This action does not contain any
information collections subject to OMB approval
[[Page 54264]]
under the Paperwork Reduction Act (PRA) (44 U.S.C. 3501 et seq.), nor
does it require any special considerations under Executive Order 12898,
entitled ``Federal Actions to Address Environmental Justice in Minority
Populations and Low-Income Populations'' (59 FR 7629, February 16,
1994).
Since tolerances and exemptions that are established on the basis
of a petition under FFDCA section 408(d), such as the tolerance in this
final rule, do not require the issuance of a proposed rule, the
requirements of the Regulatory Flexibility Act (RFA) (5 U.S.C. 601 et
seq.), do not apply.
This action directly regulates growers, food processors, food
handlers, and food retailers, not States or tribes, nor does this
action alter the relationships or distribution of power and
responsibilities established by Congress in the preemption provisions
of FFDCA section 408(n)(4). As such, the Agency has determined that
this action will not have a substantial direct effect on States or
tribal governments, on the relationship between the national government
and the States or tribal governments, or on the distribution of power
and responsibilities among the various levels of government or between
the Federal Government and Indian tribes. Thus, the Agency has
determined that Executive Order 13132, entitled ``Federalism'' (64 FR
43255, August 10, 1999) and Executive Order 13175, entitled
``Consultation and Coordination with Indian Tribal Governments'' (65 FR
67249, November 9, 2000) do not apply to this action. In addition, this
action does not impose any enforceable duty or contain any unfunded
mandate as described under Title II of the Unfunded Mandates Reform Act
(UMRA) (2 U.S.C. 1501 et seq.).
This action does not involve any technical standards that would
require Agency consideration of voluntary consensus standards pursuant
to section 12(d) of the National Technology Transfer and Advancement
Act (NTTAA) (15 U.S.C. 272 note).
VII. Congressional Review Act
Pursuant to the Congressional Review Act (5 U.S.C. 801 et seq.),
EPA will submit a report containing this rule and other required
information to the U.S. Senate, the U.S. House of Representatives, and
the Comptroller General of the United States prior to publication of
the rule in the Federal Register. This action is not a ``major rule''
as defined by 5 U.S.C. 804(2).
List of Subjects in 40 CFR Part 180
Environmental protection, Administrative practice and procedure,
Agricultural commodities, Pesticides and pests, Reporting and
recordkeeping requirements.
Dated: October 9, 2018.
Michael L. Goodis,
Director, Registration Division, Office of Pesticide Programs.
Therefore, 40 CFR chapter I is amended as follows:
PART 180--[AMENDED]
0
1. The authority citation for part 180 continues to read as follows:
Authority: 21 U.S.C. 321(q), 346a and 371.
0
2. In Sec. 180.659:
0
a. In the table in paragraph (a)(1):
0
i. Remove the entry ``Cotton, undelinted seed'';
0
ii. Add alphabetically the commodity, ''Cottonseed subgroup 20C'';
0
b. In the table in paragraph (a)(5), add alphabetically the
commodities, ``Leaf petiole vegetable subgroup 22B''; ``Peppermint,
fresh leaves''; ``Peppermint, oil''; ``Soybean, vegetable, succulent
shelled''; ``Spearmint fresh leaves''; ``Spearmint, oil''; and
``Vegetable, soybean, edible podded''; and
0
c. Revise paragraph (c).
The additions and revisions read as follows:
Sec. 180.659 Pyroxasulfone; tolerances for residues.
(a) * * *
(1) * * *
------------------------------------------------------------------------
Parts per
Commodity million
------------------------------------------------------------------------
* * * * *
Cottonseed, subgroup 20C..................................... 0.04
* * * * *
------------------------------------------------------------------------
* * * * *
(5) * * *
------------------------------------------------------------------------
Parts per
Commodity million
------------------------------------------------------------------------
* * * * *
Leaf petiole vegetable subgroup 22B.......................... 0.80
* * * * *
Peppermint, fresh leaves..................................... 0.20
Peppermint, oil.............................................. 0.70
* * * * *
Soybean, vegetable, succulent shelled........................ 0.40
Spearmint, fresh leaves...................................... 0.20
Spearmint, oil............................................... 0.70
* * * * *
Vegetable, soybean, edible podded............................ 0.40
* * * * *
------------------------------------------------------------------------
* * * * *
(c) Tolerance with regional registrations. Tolerances are
established for residues of the herbicide pyroxasulfone, including its
metabolites and degradates, in or on the commodities in the table
below. Compliance with the tolerance levels specified below is to be
determined by measuring only the sum of pyroxasulfone (3-[(5-
difluoromethoxy-1-methyl-3-(trifluoromethyl)pyrazol-4-
ylmethylsulfonyl]-4,5-dihydro-5,5-dimethyl-1,2-oxazole), and its
metabolites, M-1 (5-difluoromethoxy-1-methyl-3-trifluoromethyl-1H-
pyrazol-4-yl)methanesulfonic acid), M-3 (5-difluoromethoxy-1-methyl-3-
trifluoromethyl-1H-pyrazol-4-carboxylic acid), M-25 (5-difluoromethoxy-
3-trifluoromethyl-1H-pyrazol-4-yl)methanesulfonic acid) and M-28 (3-[1-
carboxy-2-(5,5-dimethyl-4,5-dihydroisoxazol-3-ylthio)ethylamino]-3-
oxopropanoic acid) calculated as the stoichiometric equivalent of
pyroxasulfone, in or on the commodity.
------------------------------------------------------------------------
Parts per
Commodity million
------------------------------------------------------------------------
Grass, forage................................................ 0.50
Grass, hay................................................... 1.0
------------------------------------------------------------------------
* * * * *
[FR Doc. 2018-23002 Filed 10-26-18; 8:45 am]
BILLING CODE 6560-50-P