S-metolachlor; Pesticide Tolerances, 17436-17441 [2014-07006]
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Federal Register / Vol. 79, No. 60 / Friday, March 28, 2014 / Rules and Regulations
List of Subjects
§ 85.3
28 CFR Part 36
The civil monetary penalties provided
by law within the jurisdiction of the
respective components of the
Department, as set forth in paragraphs
(a) through (d) of this section, are
adjusted in accordance with the
inflation adjustment procedures
prescribed in section 5 of the Federal
Civil Penalties Inflation Adjustment Act
of 1990, Public Law 101–410, as
follows. The adjusted penalties set forth
in paragraphs (a), (c), and (d) of this
section are effective for violations
occurring on or after September 29,
1999.
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*
*
*
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(b) Civil Rights Division. (1) 18 U.S.C.
248(c)(2)(B), Freedom of Access to
Clinic Entrances Act of 1994
(Nonviolent Physical Obstruction):
(i) The civil monetary penalty amount
for a first order for nonviolent physical
obstruction, initially set at $10,000, is
adjusted to $11,000 for a violation
occurring on or after September 29,
1999, and before April 28, 2014, and is
adjusted to $16,000 for a violation
occurring on or after April 28, 2014.
(ii) The civil monetary penalty
amount for a subsequent order for
nonviolent physical obstruction,
initially set at $15,000, is adjusted to
$16,500 for a violation occurring on or
after April 28, 2014.
(2) 18 U.S.C. 248(c)(2)(B), Freedom of
Access to Clinic Entrances Act of 1994
(Other Violations):
(i) The civil monetary penalty amount
for a first order other than for
nonviolent physical obstruction,
initially set at $15,000, is adjusted to
$16,500 for a violation occurring on or
after April 28, 2014.
(ii) The civil monetary penalty
amount for a subsequent order other
than for nonviolent physical
obstruction, initially set at $25,000, is
adjusted to $27,500 for a violation
occurring on or after September 29,
1999, and before April 28, 2014, and is
adjusted to $37,500 for a violation
occurring on or after April 28, 2014.
(3) 42 U.S.C. 3614(d)(1)(C), Fair
Housing Act of 1968, as amended
(Pattern or Practice Violation):
(i) The civil monetary penalty amount
for a first order, initially set at $50,000,
is adjusted to $55,000 for a violation
occurring on or after September 29,
1999, and before April 28, 2014, and is
adjusted to $75,000 for a violation
occurring on or after April 28, 2014.
(ii) The civil monetary penalty
amount for a subsequent order, initially
set at $100,000, is adjusted to $110,000
for a violation occurring on or after
September 29, 1999, and before April
Administrative practice and
procedure, Alcoholism, Americans with
disabilities, Buildings, Business and
industry, Civil rights, Consumer
protection, Drug abuse, Handicapped,
Historic preservation, Penalties,
Reporting and recordkeeping
requirements.
28 CFR Part 85
Penalties.
Accordingly, for the reasons set forth
in the preamble, chapter I of Title 28 of
the Code of Federal Regulations is
amended as follows:
PART 36—NONDISCRIMINATION ON
THE BASIS OF DISABILITY BY PUBLIC
ACCOMMODATIONS AND IN
COMMERCIAL FACILITIES
1. The authority citation for part 36
continues to read as follows:
■
Authority: 5 U.S.C. 301; 28 U.S.C. 509,
510; 42 U.S.C. 12188(b); Pub. L. 101–410, 104
Stat. 890, as amended by Pub. L. 104–134,
110 Stat. 1321.
2. Section 36.504 is amended by
revising paragraphs (a)(3)(i) and (ii) to
read as follows:
■
§ 36.504
Relief.
(a) * * *
(3) * * *
(i) Not exceeding $50,000 for a first
violation occurring before September
29, 1999, and not exceeding $55,000 for
a first violation occurring on or after
September 29, 1999, and before April
28, 2014, and not exceeding $75,000 for
a first violation occurring on or after
April 28, 2014.
(ii) Not exceeding $100,000 for any
subsequent violation occurring before
September 29, 1999, and not exceeding
$110,000 for any subsequent violation
occurring on or after September 29,
1999, and before April 28, 2014, and not
exceeding $150,000 for any subsequent
violation occurring on or after April 28,
2014.
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PART 85—CIVIL MONETARY
PENALTIES INFLATION ADJUSTMENT
3. The authority citation for part 85
continues to read as follows:
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■
Authority: 5 U.S.C. 301, 28 U.S.C. 503;
Pub. L. 101–410, 104 Stat. 890, as amended
by Pub. L. 104–134, 110 Stat. 1321.
4. Section 85.3 is amended by revising
the introductory text and paragraph (b)
to read as follows:
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28, 2014, and is adjusted to $150,000 for
a violation occurring on or after April
28, 2014.
(4) 50 U.S.C. App. 597(b)(3),
Servicemembers Civil Relief Act of
2003, as amended:
(i) The civil monetary penalty amount
for a first violation, initially set at
$55,000, is adjusted to $60,000 for a
violation occurring on or after April 28,
2014.
(ii) The civil monetary penalty
amount for a subsequent violation,
initially set at $110,000, is adjusted to
$120,000 for a violation occurring on or
after April 28, 2014.
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Dated: March 21, 2014.
Eric H. Holder, Jr.,
Attorney General.
[FR Doc. 2014–06979 Filed 3–27–14; 8:45 am]
BILLING CODE 4410–13–P
ENVIRONMENTAL PROTECTION
AGENCY
40 CFR Part 180
[EPA–HQ–OPP–2012–0926; FRL–9907–61]
S-metolachlor; Pesticide Tolerances
Environmental Protection
Agency (EPA).
ACTION: Final rule.
AGENCY:
This regulation amends
tolerances for residues of S-metolachlor
in or on corn, field, forage; corn, field,
stover; corn, pop, stover; corn, sweet,
forage; and corn, sweet, stover. Syngenta
Crop Protection, LLC, requested these
tolerances under the Federal Food,
Drug, and Cosmetic Act (FFDCA).
DATES: This regulation is effective
March 28, 2014. Objections and requests
for hearings must be received on or
before May 27, 2014, and must be filed
in accordance with the instructions
provided in 40 CFR part 178 (see also
Unit I.C. of the SUPPLEMENTARY
INFORMATION).
SUMMARY:
The docket for this action,
identified by docket identification (ID)
number EPA–HQ–OPP–2012–0926, 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), EPA West
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
ADDRESSES:
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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: Lois
Rossi, Registration Division (7505P),
Office of Pesticide Programs,
Environmental Protection Agency, 1200
Pennsylvania Ave. NW., Washington,
DC 20460–0001; telephone number:
(703) 305–7090; email address:
RDFRNotices@epa.gov.
SUPPLEMENTARY INFORMATION:
I. General Information
A. Does this action apply to me?
You may be potentially affected by
this action if you are an agricultural
producer, food manufacturer, or
pesticide manufacturer. The following
list of North American Industrial
Classification System (NAICS) codes is
not intended to be exhaustive, but rather
provides a guide to help readers
determine whether this document
applies to them. Potentially affected
entities may include:
• Crop production (NAICS code 111).
• Animal production (NAICS code
112).
• Food manufacturing (NAICS code
311).
• Pesticide manufacturing (NAICS
code 32532).
B. How can I get electronic access to
other related information?
You may access a frequently updated
electronic version of EPA’s tolerance
regulations at 40 CFR part 180 through
the Government Printing Office’s e-CFR
site at https://www.ecfr.gov/cgi-bin/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–2012–0926 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 May 27, 2014. Addresses for mail
and hand delivery of objections and
hearing requests are provided in 40 CFR
178.25(b).
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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–
2012–0926, 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 January 16,
2013 (78 FR 3377) (FRL–9375–4), EPA
issued a document pursuant to FFDCA
section 408(d)(3), 21 U.S.C. 346a(d)(3),
announcing the filing of a pesticide
petition (PP 2F8155) by Syngenta Crop
Protection, LLC, P.O. Box 18300,
Greensboro, NC 27419. The petition
requested that 40 CFR 180.368 be
amended by revising previously
established tolerances for residues of the
herbicide S-metolachlor, S-2-chloro-N(2-ethyl-6-methylphenyl)-N-(2-methoxy1-methylethyl)acetamide, in or on corn,
field, forage at 20 parts per million
(ppm); corn, stover at 40 ppm; and corn,
sweet, forage at 40 ppm. These
tolerances were proposed in order to
amend tolerances previously established
on these commodities at 6.0 ppm. That
document referenced a summary of the
petition prepared by Syngenta Crop
Protection, LLC, the registrant, which is
available in the docket, https://
www.regulations.gov. There were no
comments received in response to the
notice of filing.
Based upon review of the data
supporting the petition, EPA has revised
the proposed tolerance level for corn,
field, forage and has corrected the
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proposed commodity definition, corn
stover, to the following commodity
designations: Corn, field, stover; corn,
pop, stover; and corn, sweet, stover. The
reasons for these changes are explained
in Unit IV.C.
III. Aggregate Risk Assessment and
Determination of Safety
Section 408(b)(2)(A)(i) of FFDCA
allows EPA to establish a tolerance (the
legal limit for a pesticide chemical
residue in or on a food) only if EPA
determines that the tolerance is ‘‘safe.’’
Section 408(b)(2)(A)(ii) of FFDCA
defines ‘‘safe’’ to mean that ‘‘there is a
reasonable certainty that no harm will
result from aggregate exposure to the
pesticide chemical residue, including
all anticipated dietary exposures and all
other exposures for which there is
reliable information.’’ This includes
exposure through drinking water and in
residential settings, but does not include
occupational exposure. Section
408(b)(2)(C) of FFDCA requires EPA to
give special consideration to exposure
of infants and children to the pesticide
chemical residue in establishing a
tolerance and to ‘‘ensure that there is a
reasonable certainty that no harm will
result to infants and children from
aggregate exposure to the pesticide
chemical residue. . . .’’
Consistent with FFDCA section
408(b)(2)(D), and the factors specified 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 S-metolachlor
including exposure resulting from the
tolerances established by this action.
EPA’s assessment of exposures and risks
associated with S-metolachlor 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
concerning the variability of the
sensitivities of major identifiable
subgroups of consumers, including
infants and children.
The existing toxicological database is
primarily comprised of studies
conducted with metolachlor. However,
bridging studies indicate that the
metolachlor toxicology database can be
used to assess toxicity for Smetolachlor. In subchronic (metolachlor
and S-metolachlor) and chronic
(metolachlor) toxicity studies in dogs
and rats, decreased body weight and
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body weight gain were the most
commonly observed effects. No systemic
toxicity was observed when metolachlor
was administered dermally. There was
no evidence of neurotoxic effects in the
available toxicity studies, and there is
no evidence of immunotoxicity in the
submitted rat immunotoxicity study.
Prenatal developmental studies in the
rat and rabbit with both metolachlor and
S-metolachlor revealed no evidence of a
qualitative or quantitative susceptibility
in fetal animals. A 2-generation
reproduction study with metolachlor in
rats showed no evidence of parental or
reproductive toxicity. There are no
residual uncertainties with regard to
pre- and/or postnatal toxicity.
Metolachlor has been evaluated for
carcinogenic effects in the mouse and
the rat. Metolachlor did not cause an
increase in tumors of any kind in mice.
In rats, metolachlor caused an increase
in benign liver tumors in rats, but this
increase was seen only at the highest
dose tested and was statistically
significant compared to controls only in
females. There was no evidence of
mutagenic or cytogenetic effects in vivo
or in vitro. Based on this evidence, EPA
has concluded that metolachlor does not
have a common mechanism of
carcinogenicity with acetochlor and
alachlor, compounds that are
structurally similar to metolachlor.
Taking into account the qualitatively
weak evidence on carcinogenic effects
and the fact that the increase in benign
tumors in female rats occurs at a dose
1,500 times the chronic reference dose
(cRfD), EPA has concluded that the cRfD
is protective of any potential cancer
effect.
Specific information on the studies
received and the nature of the adverse
effects caused by S-metolachlor 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: ‘‘SMetolachlor, PP#2F8115. Human Health
Risk Assessment for the petition for
higher tolerances on Corn, field, forage;
Corn, sweet, forage; and Corn stover’’ at
pp. 34–46 in docket ID number EPA–
HQ–OPP–2012–0926.
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
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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://
www.epa.gov/pesticides/factsheets/
riskassess.htm. A summary of the
toxicological endpoints for Smetolachlor used for human risk
assessment is discussed in Unit III. of
the final rule published in the Federal
Register of September 17, 2010 (75 FR
56897, p. 56899) (FRL–8842–3).
C. Exposure Assessment
1. Dietary exposure from food and
feed uses. In evaluating dietary
exposure to S-metolachlor, EPA
considered exposure under the
petitioned-for tolerances as well as all
existing S-metolachlor tolerances in 40
CFR 180.368. Both the acute and
chronic analyses assume tolerance-level
residues on all crops with established,
pending, or proposed tolerances for
metolachlor and/or S-metolachlor. In
cases where separate tolerance listings
occur for both metolachlor and Smetolachlor on the same commodity,
the higher value of the two is used in
the analyses. Therefore, EPA assessed
dietary exposures from S-metolachlor 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 S-metolachlor. In estimating acute
dietary exposure, EPA used food
consumption information from the
United States Department of
Agriculture’s (USDA) Nationwide
Continuing Surveys of Food Intake by
Individuals (CSFII), 1994–1996 and
1998. As to residue levels in food, EPA
assumed tolerance-level residues for all
uses, 100 percent crop treated (PCT) for
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all commodities, and default processing
factors.
ii. Chronic exposure. In conducting
the chronic dietary exposure assessment
EPA used the food consumption data
from the USDA’s Nationwide CSFII,
1994–1996 and 1998. As to residue
levels in food, EPA assumed tolerancelevel residues for all uses, 100 PCT for
all commodities, and default processing
factors.
iii. Cancer. Based on the data
summarized in Unit III.A., EPA has
concluded that a non-linear RfD
approach is appropriate for assessing
cancer risk to S-metolachlor. Cancer risk
was assessed using the same exposure
estimates as discussed in Unit III.C.1.ii.
iv. Anticipated residue and PCT
information. EPA did not use
anticipated residue and/or PCT
information in the dietary assessment
for S-metolachlor. Tolerance level
residues and/or 100 PCT were assumed
for all food commodities.
2. Dietary exposure from drinking
water. The Agency used screening level
water exposure models in the dietary
exposure analysis and risk assessment
for S-metolachlor in drinking water.
These simulation models take into
account data on the physical, chemical,
and fate/transport characteristics of Smetolachlor. Further information
regarding EPA drinking water models
used in pesticide exposure assessment
can be found at https://www.epa.gov/
oppefed1/models/water/index.htm.
Based on the First Index Reservoir
Screening Tool (FIRST), Pesticide Root
Zone Model/Exposure Analysis
Modeling System (PRZM/EXAMS),
Screening Concentration in Ground
Water (SCI–GROW) models, and the
USGA National Water-Quality
Assessment (NAWQA) Program
monitoring data, the Agency calculated
conservative estimated drinking water
concentrations (EDWCs) of Smetolachlor and metolachlor originating
from ground water and surface water
sources. EDWCs for metolachlor and Smetolachlor were calculated for both the
parent compound, as well as the
ethanesulfonic acid (ESA) and oxanilic
acid (OA) degradates.
For surface water, PRZM/EXAMS and
FIRST Version1.1.1 models were used
for EDWCs for the parent S-metolachlor
and the ESA and OA degradates,
respectively. The SCI–GROW model
was used to predict the maximum acute
and chronic concentrations present in
shallow groundwater. Current NAWQA
monitoring data were also used to
determine EDWCs. Based on monitoring
and modeling data, total EDWCs for
acute and chronic exposures from
surface water are 219 parts per billion
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(ppb) and 119 ppb, respectively.
Groundwater EDWCs are 126 ppb for
acute and chronic exposures for noncancer assessments.
Modeled estimates of drinking water
concentrations were directly entered
into the dietary exposure model. For
acute dietary risk assessment, the water
concentration value of 219 ppb was
used to assess the contribution to
drinking water. For chronic dietary risk
assessment, the water concentration of
value 126 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). Smetolachlor is currently registered for
the following uses that could result in
residential exposures: Residential lawns
or turf by professional applicators. Smetolachlor is labeled for use on
commercial (sod farm) and residential
warm-season turf grasses and other noncrop land including golf courses, sports
fields, and ornamental gardens. Since Smetolachlor is not registered for
homeowner purchase or use, the only
potential short-term residential risk
scenario anticipated is postapplication
hand-to-mouth exposure of children
playing on treated lawns. S-metolachlor
incidental oral exposure is assumed to
include hand-to-mouth, object-tomouth, and incidental soil ingestion
exposures. No intermediate-term risk
scenarios are anticipated for the existing
and proposed uses of S-metolachlor.
Small children are the population
group of concern. Although the type of
site that S-metolachlor may be used on
varies from golf courses to ornamental
gardens, the scenario chosen for risk
assessment (residential turf use)
represents what the Agency considers
the likely upper-end of possible
exposure. Further information regarding
EPA standard assumptions and generic
inputs for residential exposures may be
found at https://www.epa.gov/pesticides/
trac/science/trac6a05.pdf.
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 S-metolachlor to share a common
mechanism of toxicity with any other
substances, and S-metolachlor does not
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appear to produce a toxic metabolite
produced by other substances. For the
purposes of this tolerance action,
therefore, EPA has assumed that Smetolachlor 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 Web site at https://
www.epa.gov/pesticides/cumulative.
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
Food Quality Protection Act Safety
Factor (FQPA SF). In applying this
provision, EPA either retains the default
value of 10X, or uses a different
additional SF when reliable data
available to EPA support the choice of
a different factor.
2. Prenatal and postnatal sensitivity.
No increase in susceptibility was seen
in developmental toxicity studies in the
rat and rabbit or in the reproductive
toxicity studies in the rat. Toxicity to
offspring was observed at dose levels
the same or greater than those causing
maternal or parental toxicity. Based on
the results of developmental and
reproductive toxicity studies, there is
not a concern for increased qualitative
and/or quantitative susceptibility
following in utero exposure to
metolachlor or S-metolachlor.
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 Smetolachlor is complete to evaluate the
safety of the tolerance.
The last rule for S-metolachlor,
published in the Federal Register of
August 15, 2012 (77 FR 48902) (FRL–
9356–9), noted that immunotoxicity and
acute and subchronic neurotoxicity
studies were required. However, since
that time, EPA has reviewed the
available hazard and exposure
information for S-metolachlor and
metolachlor and has determined that
based on the weight of the evidence
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17439
approach the acute and subchronic
neurotoxicity studies are no longer
required. Additionally, an
immunotoxicity study has been
submitted to EPA since the last
published rule. No signs of
immunotoxicity were noted in this
study at any dose level.
ii. There is no indication that Smetolachlor is a neurotoxic chemical
and there is no need for a
developmental neurotoxicity study or
additional uncertainty factors to account
for neurotoxicity.
iii. There is no evidence that Smetolachlor results in increased
susceptibility in in utero rats or rabbits
in the prenatal developmental studies or
in young rats in the 2-generation
reproduction study.
iv. There are no residual uncertainties
identified in the exposure databases.
The dietary food exposure assessments
were performed based on 100 PCT and
tolerance-level residues. EPA made
conservative (protective) assumptions in
the ground and surface water modeling
used to assess exposure to Smetolachlor in drinking water. EPA
used similarly conservative assumptions
to assess postapplication incidental oral
exposure of toddlers. These assessments
will not underestimate the exposure and
risks posed by S-metolachlor.
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, the acute dietary
exposure from food and water to Smetolachlor will occupy 1.5% of the
aPAD for all infants less than 1 year old,
the population group receiving the
greatest exposure.
2. Chronic risk. Using the exposure
assumptions described in this unit for
chronic exposure, EPA has concluded
that chronic exposure to S-metolachlor
from food and water will utilize 11.6%
of the cPAD for all infants less than 1
year old, the population group receiving
the greatest exposure. Based on the
explanation in Unit III.C.3., regarding
residential use patterns, chronic
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residential exposure to residues of Smetolachlor is not expected.
3. Short-term risk. Short-term
aggregate exposure takes into account
short-term residential exposure plus
chronic exposure to food and water
(considered to be a background
exposure level). S-metolachlor is
currently registered for uses that could
result in short-term residential
exposure, and the Agency has
determined that it is appropriate to
aggregate chronic exposure through food
and water with short-term residential
exposures to S-metolachlor.
Using the exposure assumptions
described in this unit for short-term
exposures, EPA has concluded the
combined short-term food, water, and
residential exposures result in an
aggregate MOE of 680 for children 1–2
years old. Because EPA’s level of
concern for S-metolachlor is a MOE of
100 or below, these MOEs are not of
concern.
4. Intermediate-term risk.
Intermediate-term aggregate exposure
takes into account intermediate-term
residential exposure plus chronic
exposure to food and water (considered
to be a background exposure level). An
intermediate-term adverse effect was
identified; however, S-metolachlor is
not registered for any use patterns that
would result in intermediate-term
residential exposure. Intermediate-term
risk is assessed based on intermediateterm residential exposure plus chronic
dietary exposure. Because there is no
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 intermediate-term risk), no
further assessment of intermediate-term
risk is necessary, and EPA relies on the
chronic dietary risk assessment for
evaluating intermediate-term risk for Smetolachlor.
5. Aggregate cancer risk for U.S.
population. As explained in Unit III.A.,
EPA has concluded that the cRfD is
protective of cancer effects. As
previously discussed, the chronic risk
assessment indicated that aggregate
exposure to S-metolachlor does not pose
a risk of concern.
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 Smetolachlor residues.
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16:20 Mar 27, 2014
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IV. Other Considerations
V. Conclusion
A. Analytical Enforcement Methodology
Adequate enforcement methodologies
are available to enforce the tolerance
expression, including: a gas
chromatography with nitrogen
phosphorous detector (GC/NPD) method
(Method I) for determining residues in
or on crop commodities; and a gas
chromatography with mass
spectroscopy detector (GC/MSD)
method (Method II) for determining
residues in livestock commodities.
The method may be requested from:
Chief, Analytical Chemistry Branch,
Environmental Science Center, 701
Mapes Rd., Ft. Meade, MD 20755–5350;
telephone number: (410) 305–2905;
email address: residuemethods@
epa.gov.
Therefore, tolerances are amended for
residues of S-metolachlor, S-2-chloro-N(2-ethyl-6-methylphenyl)-N-(2-methoxy1-methylethyl)acetamide, from 6.0 ppm
to 40 ppm in or on the following
commodities: Corn, field, forage; corn,
field, stover; corn, pop, stover; corn,
sweet, forage; and corn, sweet, stover.
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 MRLs
for S-metolachlor.
C. Revisions to Petitioned-For
Tolerances
Based on the available forage residue
data submitted with the petition, EPA
revised the proposed tolerance on corn,
field, forage from 20 ppm to 40 ppm.
The available data indicate that 20 ppm
would not be sufficient to cover likely
residues in corn, field, forage at
approved application rates; a tolerance
at 40 ppm is supported by the available
residue data. Additionally, the proposed
tolerance for corn stover has been
revised to the following commodity
entries: Corn, field, stover; corn, pop,
stover; and corn, sweet, stover. This
revision was made in order to accurately
capture the correct commodity
terminology for regulated corn stover
commodities.
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VI. Statutory and Executive Order
Reviews
This final rule 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 final rule
has been exempted from review under
Executive Order 12866, this final rule is
not subject to Executive Order 13211,
entitled ‘‘Actions Concerning
Regulations That Significantly Affect
Energy Supply, Distribution, or Use’’ (66
FR 28355, May 22, 2001) or Executive
Order 13045, entitled ‘‘Protection of
Children from Environmental Health
Risks and Safety Risks’’ (62 FR 19885,
April 23, 1997). This 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 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 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 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
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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 final rule.
In addition, this final 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) (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 of 1995
(NTTAA) (15 U.S.C. 272 note).
VII. Congressional Review Act
Pursuant to the Congressional Review
Act (5 U.S.C. 801 et seq.), EPA will
submit a report containing this rule and
other required information to the U.S.
Senate, the U.S. House of
Representatives, and the Comptroller
General of the United States prior to
publication of the rule in the Federal
Register. This action is not a ‘‘major
rule’’ as defined by 5 U.S.C. 804(2).
List of Subjects in 40 CFR Part 180
Environmental protection,
Administrative practice and procedure,
Agricultural commodities, Pesticides
and pests, Reporting and recordkeeping
requirements.
Dated: March 21, 2014.
Lois Rossi,
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 § 180.368, revise the following
entries in the table in paragraph (a)(2) to
read as follows:
■
§ 180.368 Metolachlor; tolerances for
residues.
tkelley on DSK3SPTVN1PROD with RULES
(a) * * *
(2) * * *
Parts per
million
Commodity
*
*
*
Corn, field, forage .................
Corn, field, stover .................
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*
*
40
40
Jkt 232001
17441
• https://www.regulations.gov. Follow
online instructions for submitting
comments.
*
*
*
*
*
• Email: Howard Caine, Remedial
Corn, pop, stover ..................
40 Project Manager, at howard.caine@
Corn, sweet, forage ..............
40 epa.gov or Susan Pastor, Community
Involvement Coordinator, at
*
*
*
*
*
Corn, sweet, stover ...............
40 pastor.susan@epa.gov.
• Fax: Gladys Beard, NPL Deletion
Process Manager at (312) 886–4071.
*
*
*
*
*
• Mail: Howard Caine, Remedial
Project Manager, U.S. Environmental
*
*
*
*
*
Protection Agency (SR–6J), 77 West
[FR Doc. 2014–07006 Filed 3–27–14; 8:45 am]
Jackson Boulevard, Chicago, IL 60604,
BILLING CODE 6560–50–P
(312) 353–9685, or Susan Pastor,
Community Involvement Coordinator,
ENVIRONMENTAL PROTECTION
U.S. Environmental Protection Agency
AGENCY
(SI–7J), 77 West Jackson Boulevard,
Chicago, IL 60604, (312) 353–1325 or
40 CFR Part 300
(800) 621–8431.
• Hand delivery: Susan Pastor,
[EPA–HQ–SFUND–2005–0011; FRL–9908–
Community Involvement Coordinator,
65-Region 5]
U.S. Environmental Protection Agency
National Oil and Hazardous Substance (SI–7J), 77 West Jackson Boulevard,
Pollution Contingency Plan; National
Chicago, IL 60604. Such deliveries are
Priorities List: Deletion of the Eau
only accepted during the docket’s
Claire Municipal Well Field Superfund
normal hours of operation, and special
arrangements should be made for
Site
deliveries of boxed information. The
AGENCY: Environmental Protection
normal business hours are Monday
Agency.
through Friday, 8:30 a.m. to 4:30 p.m.
ACTION: Direct final rule.
CST, excluding federal holidays.
Instructions: Direct your comments to
SUMMARY: The U.S. Environmental
Docket ID no. EPA–HQ–SFUND–2005–
Protection Agency (EPA) Region 5 is
0011. EPA’s policy is that all comments
publishing a direct final notice of
received will be included in the public
deletion of the Eau Claire Municipal
Well Field Superfund Site (Site) located docket without change and may be
made available online at https://
in Eau Claire, Wisconsin, from the
www.regulations.gov, including any
National Priorities List (NPL). The NPL,
personal information provided, unless
promulgated pursuant to Section 105 of
the comment includes information
the Comprehensive Environmental
claimed to be Confidential Business
Response, Compensation, and Liability
Information (CBI) or other information
Act (CERCLA) of 1980, as amended, is
whose disclosure is restricted by statute.
an appendix to the National Oil and
Do not submit information that you
Hazardous Substances Pollution
consider to be CBI or otherwise
Contingency Plan (NCP). This direct
protected through https://
final deletion is being published by EPA
www.regulations.gov or email. The
with the concurrence of the State of
https://www.regulations.gov Web site is
Wisconsin, through the Wisconsin
an ‘‘anonymous access’’ system, which
Department of Natural Resources
means EPA will not know your identity
(WDNR), because EPA has determined
or contact information unless you
that all appropriate response actions
provide it in the body of your comment.
under CERCLA have been completed.
If you send an email comment directly
However, this deletion does not
to EPA without going through https://
preclude future actions under
www.regulations.gov, your email
Superfund.
address will be automatically captured
DATES: This direct final deletion is
and included as part of the comment
effective May 27, 2014 unless EPA
that is placed in the public docket and
receives adverse comments by April 28, made available on the Internet. If you
2014. If adverse comments are received, submit an electronic comment, EPA
EPA will publish a timely withdrawal of recommends that you include your
the direct final deletion in the Federal
name and other contact information in
Register informing the public that the
the body of your comment and with any
deletion will not take effect.
disk or CD–ROM you submit. If EPA
ADDRESSES: Submit your comments,
cannot read your comment due to
identified by Docket ID no. EPA–HQ–
technical difficulties and cannot contact
SFUND–2005–0011, by one of the
you for clarification, EPA may not be
following methods:
able to consider your comment.
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million
Commodity
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Agencies
[Federal Register Volume 79, Number 60 (Friday, March 28, 2014)]
[Rules and Regulations]
[Pages 17436-17441]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2014-07006]
=======================================================================
-----------------------------------------------------------------------
ENVIRONMENTAL PROTECTION AGENCY
40 CFR Part 180
[EPA-HQ-OPP-2012-0926; FRL-9907-61]
S-metolachlor; Pesticide Tolerances
AGENCY: Environmental Protection Agency (EPA).
ACTION: Final rule.
-----------------------------------------------------------------------
SUMMARY: This regulation amends tolerances for residues of S-
metolachlor in or on corn, field, forage; corn, field, stover; corn,
pop, stover; corn, sweet, forage; and corn, sweet, stover. Syngenta
Crop Protection, LLC, requested these tolerances under the Federal
Food, Drug, and Cosmetic Act (FFDCA).
DATES: This regulation is effective March 28, 2014. Objections and
requests for hearings must be received on or before May 27, 2014, 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-2012-0926, 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), EPA West 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
[[Page 17437]]
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: Lois Rossi, Registration Division
(7505P), Office of Pesticide Programs, Environmental Protection Agency,
1200 Pennsylvania Ave. NW., Washington, DC 20460-0001; telephone
number: (703) 305-7090; email address: RDFRNotices@epa.gov.
SUPPLEMENTARY INFORMATION:
I. General Information
A. Does this action apply to me?
You may be potentially affected by this action if you are an
agricultural producer, food manufacturer, or pesticide manufacturer.
The following list of North American Industrial Classification System
(NAICS) codes is not intended to be exhaustive, but rather provides a
guide to help readers determine whether this document applies to them.
Potentially affected entities may include:
Crop production (NAICS code 111).
Animal production (NAICS code 112).
Food manufacturing (NAICS code 311).
Pesticide manufacturing (NAICS code 32532).
B. How can I get electronic access to other related information?
You may access a frequently updated electronic version of EPA's
tolerance regulations at 40 CFR part 180 through the Government
Printing Office's e-CFR site at https://www.ecfr.gov/cgi-bin/text-idx?&c=ecfr&tpl=/ecfrbrowse/Title40/40tab_02.tpl.
C. How can I file an objection or hearing request?
Under FFDCA section 408(g), 21 U.S.C. 346a, any person may file an
objection to any aspect of this regulation and may also request a
hearing on those objections. You must file your objection or request a
hearing on this regulation in accordance with the instructions provided
in 40 CFR part 178. To ensure proper receipt by EPA, you must identify
docket ID number EPA-HQ-OPP-2012-0926 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
May 27, 2014. 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-2012-0926, 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 January 16, 2013 (78 FR 3377) (FRL-9375-
4), EPA issued a document pursuant to FFDCA section 408(d)(3), 21
U.S.C. 346a(d)(3), announcing the filing of a pesticide petition (PP
2F8155) by Syngenta Crop Protection, LLC, P.O. Box 18300, Greensboro,
NC 27419. The petition requested that 40 CFR 180.368 be amended by
revising previously established tolerances for residues of the
herbicide S-metolachlor, S-2-chloro-N-(2-ethyl-6-methylphenyl)-N-(2-
methoxy-1-methylethyl)acetamide, in or on corn, field, forage at 20
parts per million (ppm); corn, stover at 40 ppm; and corn, sweet,
forage at 40 ppm. These tolerances were proposed in order to amend
tolerances previously established on these commodities at 6.0 ppm. That
document referenced a summary of the petition prepared by Syngenta Crop
Protection, LLC, the registrant, which is available in the docket,
https://www.regulations.gov. There were no comments received in response
to the notice of filing.
Based upon review of the data supporting the petition, EPA has
revised the proposed tolerance level for corn, field, forage and has
corrected the proposed commodity definition, corn stover, to the
following commodity designations: Corn, field, stover; corn, pop,
stover; and corn, sweet, stover. The reasons for these changes are
explained in Unit IV.C.
III. Aggregate Risk Assessment and Determination of Safety
Section 408(b)(2)(A)(i) of FFDCA allows EPA to establish a
tolerance (the legal limit for a pesticide chemical residue in or on a
food) only if EPA determines that the tolerance is ``safe.'' Section
408(b)(2)(A)(ii) of FFDCA defines ``safe'' to mean that ``there is a
reasonable certainty that no harm will result from aggregate exposure
to the pesticide chemical residue, including all anticipated dietary
exposures and all other exposures for which there is reliable
information.'' This includes exposure through drinking water and in
residential settings, but does not include occupational exposure.
Section 408(b)(2)(C) of FFDCA requires EPA to give special
consideration to exposure of infants and children to the pesticide
chemical residue in establishing a tolerance and to ``ensure that there
is a reasonable certainty that no harm will result to infants and
children from aggregate exposure to the pesticide chemical residue. . .
.''
Consistent with FFDCA section 408(b)(2)(D), and the factors
specified 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 S-metolachlor including
exposure resulting from the tolerances established by this action.
EPA's assessment of exposures and risks associated with S-metolachlor
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 concerning the variability of the sensitivities
of major identifiable subgroups of consumers, including infants and
children.
The existing toxicological database is primarily comprised of
studies conducted with metolachlor. However, bridging studies indicate
that the metolachlor toxicology database can be used to assess toxicity
for S-metolachlor. In subchronic (metolachlor and S-metolachlor) and
chronic (metolachlor) toxicity studies in dogs and rats, decreased body
weight and
[[Page 17438]]
body weight gain were the most commonly observed effects. No systemic
toxicity was observed when metolachlor was administered dermally. There
was no evidence of neurotoxic effects in the available toxicity
studies, and there is no evidence of immunotoxicity in the submitted
rat immunotoxicity study. Prenatal developmental studies in the rat and
rabbit with both metolachlor and S-metolachlor revealed no evidence of
a qualitative or quantitative susceptibility in fetal animals. A 2-
generation reproduction study with metolachlor in rats showed no
evidence of parental or reproductive toxicity. There are no residual
uncertainties with regard to pre- and/or postnatal toxicity.
Metolachlor has been evaluated for carcinogenic effects in the
mouse and the rat. Metolachlor did not cause an increase in tumors of
any kind in mice. In rats, metolachlor caused an increase in benign
liver tumors in rats, but this increase was seen only at the highest
dose tested and was statistically significant compared to controls only
in females. There was no evidence of mutagenic or cytogenetic effects
in vivo or in vitro. Based on this evidence, EPA has concluded that
metolachlor does not have a common mechanism of carcinogenicity with
acetochlor and alachlor, compounds that are structurally similar to
metolachlor. Taking into account the qualitatively weak evidence on
carcinogenic effects and the fact that the increase in benign tumors in
female rats occurs at a dose 1,500 times the chronic reference dose
(cRfD), EPA has concluded that the cRfD is protective of any potential
cancer effect.
Specific information on the studies received and the nature of the
adverse effects caused by S-metolachlor 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: ``S-Metolachlor, PP2F8115.
Human Health Risk Assessment for the petition for higher tolerances on
Corn, field, forage; Corn, sweet, forage; and Corn stover'' at pp. 34-
46 in docket ID number EPA-HQ-OPP-2012-0926.
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://www.epa.gov/pesticides/factsheets/riskassess.htm. A summary of the toxicological
endpoints for S-metolachlor used for human risk assessment is discussed
in Unit III. of the final rule published in the Federal Register of
September 17, 2010 (75 FR 56897, p. 56899) (FRL-8842-3).
C. Exposure Assessment
1. Dietary exposure from food and feed uses. In evaluating dietary
exposure to S-metolachlor, EPA considered exposure under the
petitioned-for tolerances as well as all existing S-metolachlor
tolerances in 40 CFR 180.368. Both the acute and chronic analyses
assume tolerance-level residues on all crops with established, pending,
or proposed tolerances for metolachlor and/or S-metolachlor. In cases
where separate tolerance listings occur for both metolachlor and S-
metolachlor on the same commodity, the higher value of the two is used
in the analyses. Therefore, EPA assessed dietary exposures from S-
metolachlor 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 S-metolachlor. In estimating acute dietary exposure, EPA used food
consumption information from the United States Department of
Agriculture's (USDA) Nationwide Continuing Surveys of Food Intake by
Individuals (CSFII), 1994-1996 and 1998. As to residue levels in food,
EPA assumed tolerance-level residues for all uses, 100 percent crop
treated (PCT) for all commodities, and default processing factors.
ii. Chronic exposure. In conducting the chronic dietary exposure
assessment EPA used the food consumption data from the USDA's
Nationwide CSFII, 1994-1996 and 1998. As to residue levels in food, EPA
assumed tolerance-level residues for all uses, 100 PCT for all
commodities, and default processing factors.
iii. Cancer. Based on the data summarized in Unit III.A., EPA has
concluded that a non-linear RfD approach is appropriate for assessing
cancer risk to S-metolachlor. Cancer risk was assessed using the same
exposure estimates as discussed in Unit III.C.1.ii.
iv. Anticipated residue and PCT information. EPA did not use
anticipated residue and/or PCT information in the dietary assessment
for S-metolachlor. Tolerance level residues and/or 100 PCT were assumed
for all food commodities.
2. Dietary exposure from drinking water. The Agency used screening
level water exposure models in the dietary exposure analysis and risk
assessment for S-metolachlor in drinking water. These simulation models
take into account data on the physical, chemical, and fate/transport
characteristics of S-metolachlor. Further information regarding EPA
drinking water models used in pesticide exposure assessment can be
found at https://www.epa.gov/oppefed1/models/water/index.htm.
Based on the First Index Reservoir Screening Tool (FIRST),
Pesticide Root Zone Model/Exposure Analysis Modeling System (PRZM/
EXAMS), Screening Concentration in Ground Water (SCI-GROW) models, and
the USGA National Water-Quality Assessment (NAWQA) Program monitoring
data, the Agency calculated conservative estimated drinking water
concentrations (EDWCs) of S-metolachlor and metolachlor originating
from ground water and surface water sources. EDWCs for metolachlor and
S-metolachlor were calculated for both the parent compound, as well as
the ethanesulfonic acid (ESA) and oxanilic acid (OA) degradates.
For surface water, PRZM/EXAMS and FIRST Version1.1.1 models were
used for EDWCs for the parent S-metolachlor and the ESA and OA
degradates, respectively. The SCI-GROW model was used to predict the
maximum acute and chronic concentrations present in shallow
groundwater. Current NAWQA monitoring data were also used to determine
EDWCs. Based on monitoring and modeling data, total EDWCs for acute and
chronic exposures from surface water are 219 parts per billion
[[Page 17439]]
(ppb) and 119 ppb, respectively. Groundwater EDWCs are 126 ppb for
acute and chronic exposures for non-cancer assessments.
Modeled estimates of drinking water concentrations were directly
entered into the dietary exposure model. For acute dietary risk
assessment, the water concentration value of 219 ppb was used to assess
the contribution to drinking water. For chronic dietary risk
assessment, the water concentration of value 126 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). S-metolachlor is
currently registered for the following uses that could result in
residential exposures: Residential lawns or turf by professional
applicators. S-metolachlor is labeled for use on commercial (sod farm)
and residential warm-season turf grasses and other non-crop land
including golf courses, sports fields, and ornamental gardens. Since S-
metolachlor is not registered for homeowner purchase or use, the only
potential short-term residential risk scenario anticipated is
postapplication hand-to-mouth exposure of children playing on treated
lawns. S-metolachlor incidental oral exposure is assumed to include
hand-to-mouth, object-to-mouth, and incidental soil ingestion
exposures. No intermediate-term risk scenarios are anticipated for the
existing and proposed uses of S-metolachlor.
Small children are the population group of concern. Although the
type of site that S-metolachlor may be used on varies from golf courses
to ornamental gardens, the scenario chosen for risk assessment
(residential turf use) represents what the Agency considers the likely
upper-end of possible exposure. Further information regarding EPA
standard assumptions and generic inputs for residential exposures may
be found at https://www.epa.gov/pesticides/trac/science/trac6a05.pdf.
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 S-
metolachlor to share a common mechanism of toxicity with any other
substances, and S-metolachlor does not appear to produce a toxic
metabolite produced by other substances. For the purposes of this
tolerance action, therefore, EPA has assumed that S-metolachlor 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 Web site at https://www.epa.gov/pesticides/cumulative.
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 Food Quality
Protection Act Safety Factor (FQPA SF). In applying this provision, EPA
either retains the default value of 10X, or uses a different additional
SF when reliable data available to EPA support the choice of a
different factor.
2. Prenatal and postnatal sensitivity. No increase in
susceptibility was seen in developmental toxicity studies in the rat
and rabbit or in the reproductive toxicity studies in the rat. Toxicity
to offspring was observed at dose levels the same or greater than those
causing maternal or parental toxicity. Based on the results of
developmental and reproductive toxicity studies, there is not a concern
for increased qualitative and/or quantitative susceptibility following
in utero exposure to metolachlor or S-metolachlor.
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 S-metolachlor is complete to evaluate
the safety of the tolerance.
The last rule for S-metolachlor, published in the Federal Register
of August 15, 2012 (77 FR 48902) (FRL-9356-9), noted that
immunotoxicity and acute and subchronic neurotoxicity studies were
required. However, since that time, EPA has reviewed the available
hazard and exposure information for S-metolachlor and metolachlor and
has determined that based on the weight of the evidence approach the
acute and subchronic neurotoxicity studies are no longer required.
Additionally, an immunotoxicity study has been submitted to EPA since
the last published rule. No signs of immunotoxicity were noted in this
study at any dose level.
ii. There is no indication that S-metolachlor is a neurotoxic
chemical and there is no need for a developmental neurotoxicity study
or additional uncertainty factors to account for neurotoxicity.
iii. There is no evidence that S-metolachlor results in increased
susceptibility in in utero rats or rabbits in the prenatal
developmental studies or in young rats in the 2-generation reproduction
study.
iv. There are no residual uncertainties identified in the exposure
databases. The dietary food exposure assessments were performed based
on 100 PCT and tolerance-level residues. EPA made conservative
(protective) assumptions in the ground and surface water modeling used
to assess exposure to S-metolachlor in drinking water. EPA used
similarly conservative assumptions to assess postapplication incidental
oral exposure of toddlers. These assessments will not underestimate the
exposure and risks posed by S-metolachlor.
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, the acute dietary exposure from food and water
to S-metolachlor will occupy 1.5% of the aPAD for all infants less than
1 year old, the population group receiving the greatest exposure.
2. Chronic risk. Using the exposure assumptions described in this
unit for chronic exposure, EPA has concluded that chronic exposure to
S-metolachlor from food and water will utilize 11.6% of the cPAD for
all infants less than 1 year old, the population group receiving the
greatest exposure. Based on the explanation in Unit III.C.3., regarding
residential use patterns, chronic
[[Page 17440]]
residential exposure to residues of S-metolachlor is not expected.
3. Short-term risk. Short-term aggregate exposure takes into
account short-term residential exposure plus chronic exposure to food
and water (considered to be a background exposure level). S-metolachlor
is currently registered for uses that could result in short-term
residential exposure, and the Agency has determined that it is
appropriate to aggregate chronic exposure through food and water with
short-term residential exposures to S-metolachlor.
Using the exposure assumptions described in this unit for short-
term exposures, EPA has concluded the combined short-term food, water,
and residential exposures result in an aggregate MOE of 680 for
children 1-2 years old. Because EPA's level of concern for S-
metolachlor is a MOE of 100 or below, these MOEs are not of concern.
4. Intermediate-term risk. Intermediate-term aggregate exposure
takes into account intermediate-term residential exposure plus chronic
exposure to food and water (considered to be a background exposure
level). An intermediate-term adverse effect was identified; however, S-
metolachlor is not registered for any use patterns that would result in
intermediate-term residential exposure. Intermediate-term risk is
assessed based on intermediate-term residential exposure plus chronic
dietary exposure. Because there is no 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 intermediate-term risk), no further assessment
of intermediate-term risk is necessary, and EPA relies on the chronic
dietary risk assessment for evaluating intermediate-term risk for S-
metolachlor.
5. Aggregate cancer risk for U.S. population. As explained in Unit
III.A., EPA has concluded that the cRfD is protective of cancer
effects. As previously discussed, the chronic risk assessment indicated
that aggregate exposure to S-metolachlor does not pose a risk of
concern.
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 S-metolachlor residues.
IV. Other Considerations
A. Analytical Enforcement Methodology
Adequate enforcement methodologies are available to enforce the
tolerance expression, including: a gas chromatography with nitrogen
phosphorous detector (GC/NPD) method (Method I) for determining
residues in or on crop commodities; and a gas chromatography with mass
spectroscopy detector (GC/MSD) method (Method II) for determining
residues in livestock commodities.
The method may be requested from: Chief, Analytical Chemistry
Branch, Environmental Science Center, 701 Mapes Rd., Ft. Meade, MD
20755-5350; telephone number: (410) 305-2905; email address:
residuemethods@epa.gov.
B. International Residue Limits
In making its tolerance decisions, EPA seeks to harmonize U.S.
tolerances with international standards whenever possible, consistent
with U.S. food safety standards and agricultural practices. EPA
considers the international maximum residue limits (MRLs) established
by the Codex Alimentarius Commission (Codex), as required by FFDCA
section 408(b)(4). The Codex Alimentarius is a joint United Nations
Food and Agriculture Organization/World Health Organization food
standards program, and it is recognized as an international food safety
standards-setting organization in trade agreements to which the United
States is a party. EPA may establish a tolerance that is different from
a Codex MRL; however, FFDCA section 408(b)(4) requires that EPA explain
the reasons for departing from the Codex level.
The Codex has not established MRLs for S-metolachlor.
C. Revisions to Petitioned-For Tolerances
Based on the available forage residue data submitted with the
petition, EPA revised the proposed tolerance on corn, field, forage
from 20 ppm to 40 ppm. The available data indicate that 20 ppm would
not be sufficient to cover likely residues in corn, field, forage at
approved application rates; a tolerance at 40 ppm is supported by the
available residue data. Additionally, the proposed tolerance for corn
stover has been revised to the following commodity entries: Corn,
field, stover; corn, pop, stover; and corn, sweet, stover. This
revision was made in order to accurately capture the correct commodity
terminology for regulated corn stover commodities.
V. Conclusion
Therefore, tolerances are amended for residues of S-metolachlor, S-
2-chloro-N-(2-ethyl-6-methylphenyl)-N-(2-methoxy-1-
methylethyl)acetamide, from 6.0 ppm to 40 ppm in or on the following
commodities: Corn, field, forage; corn, field, stover; corn, pop,
stover; corn, sweet, forage; and corn, sweet, stover.
VI. Statutory and Executive Order Reviews
This final rule 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 final rule has
been exempted from review under Executive Order 12866, this final rule
is not subject to Executive Order 13211, entitled ``Actions Concerning
Regulations That Significantly Affect Energy Supply, Distribution, or
Use'' (66 FR 28355, May 22, 2001) or Executive Order 13045, entitled
``Protection of Children from Environmental Health Risks and Safety
Risks'' (62 FR 19885, April 23, 1997). This 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 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 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 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
[[Page 17441]]
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 final rule. In addition, this final 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) (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 of 1995 (NTTAA) (15 U.S.C. 272 note).
VII. Congressional Review Act
Pursuant to the Congressional Review Act (5 U.S.C. 801 et seq.),
EPA will submit a report containing this rule and other required
information to the U.S. Senate, the U.S. House of Representatives, and
the Comptroller General of the United States prior to publication of
the rule in the Federal Register. This action is not a ``major rule''
as defined by 5 U.S.C. 804(2).
List of Subjects in 40 CFR Part 180
Environmental protection, Administrative practice and procedure,
Agricultural commodities, Pesticides and pests, Reporting and
recordkeeping requirements.
Dated: March 21, 2014.
Lois Rossi,
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. 180.368, revise the following entries in the table in
paragraph (a)(2) to read as follows:
Sec. 180.368 Metolachlor; tolerances for residues.
(a) * * *
(2) * * *
------------------------------------------------------------------------
Parts per
Commodity million
------------------------------------------------------------------------
* * * * *
Corn, field, forage..................................... 40
Corn, field, stover..................................... 40
* * * * *
Corn, pop, stover....................................... 40
Corn, sweet, forage..................................... 40
* * * * *
Corn, sweet, stover..................................... 40
* * * * *
------------------------------------------------------------------------
* * * * *
[FR Doc. 2014-07006 Filed 3-27-14; 8:45 am]
BILLING CODE 6560-50-P