Aldicarb, Bensulide, Coumaphos, Ethalfluralin, and Pirimiphos-methyl Registration Review; Draft Human Health and Ecological Risk Assessments; Notice of Availability, 24610-24613 [2016-09732]
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Federal Register / Vol. 81, No. 80 / Tuesday, April 26, 2016 / Notices
1. 8917–EUP–2. (EPA–HQ–OPP–
2015–0516). Amendment and
Extension. J.R. Simplot Co., 5369 W.
[EPA–HQ–OPP–2015–0163; FRL–9944–95]
Irving St., Boise, ID 83706. This EUP
allows the use of 13,000,000 pounds of
Amendments, Extensions, and/or
Issuances of Experimental Use Permits seed potatoes containing 0.390 pound of
VNT1 protein (or 3.90 × 10¥1 pound of
AGENCY: Environmental Protection
VNT1 protein) on 5,576 acres (i.e., 5,200
Agency (EPA).
Rpi-vnt1 plant-incorporated protectant
(PIP) acres and 376 maximum border
ACTION: Notice.
acres) to evaluate resistance to
SUMMARY: EPA has granted
Phytophthora infestans (commonly
amendments, extensions, and/or
known as late potato blight). The
issuances of experimental use permits
program is authorized only in the states
(EUPs) to the pesticide applicants
of Arizona, California, Colorado,
described in Unit II of the
Florida, Hawaii, Idaho, Illinois, Indiana,
SUPPLEMENTARY INFORMATION. An EUP
Kansas, Maine, Michigan, Minnesota,
permits use of a pesticide for
Missouri, Nebraska, Nevada, New
experimental or research purposes only
Mexico, New York, North Carolina,
in accordance with the limitations in
North Dakota, Oregon, Pennsylvania,
the permit.
South Carolina, Texas, Utah,
Washington, and Wisconsin. The EUP is
FOR FURTHER INFORMATION CONTACT:
effective from December 17, 2015, to
Robert McNally, Biopesticides and
April 1, 2017.
Pollution Prevention Division (7511P),
2. 62719–EUP–66. (EPA–HQ–OPP–
Office of Pesticide Programs,
2014–0521). Amendment and
Environmental Protection Agency, 1200
Extension. Dow AgroSciences, LLC,
Pennsylvania Ave. NW., Washington,
9330 Zionsville Rd., Indianapolis, IN
DC 20460–0001; main telephone
number: (703) 305–7090; email address: 46268–1054. This EUP allows the use of
8.509 pounds of active ingredient
BPPDFRNotices@epa.gov.
(0.399, 0.120, 9.364 × 10¥7, 0.448, 6.22,
SUPPLEMENTARY INFORMATION:
0.152, and 1.17 pounds of Bacillus
I. General Information
thuringiensis (Bt) Cry1A.105 protein, Bt
Cry2Ab2 protein, DvSnf7 doubleA. Does this action apply to me?
stranded RNA (dsRNA), Bt Cry1F
This action is directed to the public
protein, Bt Cry34Ab1 protein, Bt
in general. Although this action may be
Cry35Ab1 protein, and Bt Cry3Bb1
of particular interest to those persons
protein, respectively) in 456,699 pounds
who conduct or sponsor research on
of corn seed and involves 5,844 acres
pesticides, EPA has not attempted to
(i.e., 2,660 PIP acres, 1,312 non-PIP
describe all the specific entities that
acres, and 1,872 border acres) for inbred
may be affected by this action.
and hybrid development, nursery
observations, and testing and collection
B. How can I get copies of this document
of product characterization data. The
and other related information?
program is authorized only in the
The dockets for these actions,
commonwealth of Puerto Rico and in
identified by the docket identification
the states of Arkansas, California,
(ID) numbers as shown in the body of
Georgia, Hawaii, Illinois, Indiana, Iowa,
this document, are available at https://
Kansas, Minnesota, Missouri, Nebraska,
www.regulations.gov or at the Office of
North Carolina, North Dakota, Ohio,
Pesticide Programs Regulatory Public
Oklahoma, Pennsylvania, South
Docket (OPP Docket) in the
Carolina, South Dakota, Texas, and
Environmental Protection Agency
Wisconsin. The EUP is effective from
Docket Center (EPA/DC), West William
March 4, 2016, to March 31, 2017.
3. 88877–EUP–2. (EPA–HQ–OPP–
Jefferson Clinton Bldg., Rm. 3334, 1301
Constitution Ave. NW., Washington, DC 2015–0374). Issuance. University of
Kentucky, Department of Entomology,
20460–0001. The Public Reading Room
S–225 Agricultural Science Center
is open from 8:30 a.m. to 4:30 p.m.,
Monday through Friday, excluding legal North, Lexington, KY 40546–0091. This
holidays. The telephone number for the EUP allows the use of 2,400,000 male
Public Reading Room is (202) 566–1744, Aedes aegypti WB1 Strain mosquitoes
weighing 5.672 ounces and containing
and the telephone number for the OPP
Docket is (703) 305–5805. Please review 5.672 × 10¥5 ounce of the active
ingredient Wolbachia pipientis, wAlbB
the visitor instructions and additional
Strain to evaluate the active ingredient’s
information about the docket available
effectiveness in suppressing and
at https://www.epa.gov/dockets.
eliminating Aedes aegypti mosquitoes.
II. EUPs
The program is authorized only in the
EPA has issued the following EUPs:
state of California over 840 acres
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ENVIRONMENTAL PROTECTION
AGENCY
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(release and surveillance/monitoring
acreage). The EUP is effective from
October 15, 2015, to December 31, 2016.
EPA received two comments, a positive
one from the Consolidated Mosquito
Abatement District in California and a
negative one that was anonymous. As
the anonymous commenter did not
specify any particular safety concern
with regard to this EUP’s issuance, the
comment was not considered further.
Authority: 7 U.S.C. 136 et seq.
Dated: April 18, 2016.
Robert C. McNally,
Director, Biopesticides and Pollution
Prevention Division, Office of Pesticide
Programs.
[FR Doc. 2016–09744 Filed 4–25–16; 8:45 am]
BILLING CODE 6560–50–P
ENVIRONMENTAL PROTECTION
AGENCY
[EPA–HQ–OPP–2015–0794; FRL–9943–82]
Aldicarb, Bensulide, Coumaphos,
Ethalfluralin, and Pirimiphos-methyl
Registration Review; Draft Human
Health and Ecological Risk
Assessments; Notice of Availability
Environmental Protection
Agency (EPA).
ACTION: Notice.
AGENCY:
This notice announces the
availability of EPA’s draft human health
risk and draft ecological risk
assessments for aldicarb, bensulide,
coumaphos, ethalfluralin, and
pirimiphos-methyl and opens a public
comment period on these documents.
Registration review is EPA’s periodic
review of pesticide registrations to
ensure that each pesticide continues to
satisfy the statutory standard for
registration, that is, the pesticide can
perform its intended function without
unreasonable adverse effects on human
health or the environment. As part of
the registration review process, the
Agency has completed a comprehensive
draft human health and ecological risk
assessments for all aldicarb, bensulide,
coumaphos, ethalfluralin, and
pirimiphos-methyl uses. After reviewing
comments received during the public
comment period, EPA will issue a
revised risk assessment, explain any
changes to the draft risk assessment, and
respond to comments and may request
public input on risk mitigation before
completing a proposed registration
review decision for aldicarb, bensulide,
coumaphos, ethalfluralin, and
pirimiphos-methyl. Through this
program, EPA is ensuring that each
pesticide’s registration is based on
SUMMARY:
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Federal Register / Vol. 81, No. 80 / Tuesday, April 26, 2016 / Notices
current scientific and other knowledge,
including its effects on human health
and the environment.
DATES: Comments must be received on
or before June 27, 2016.
ADDRESSES: Submit your comments,
identified by docket identification (ID)
number EPA–HQ–OPP–2015–0794, 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
Confidential Business Information (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.
FOR FURTHER INFORMATION CONTACT: For
pesticide specific information contact:
The Chemical Review Manager listed in
Table 1of Unit III.
For general questions on the
registration review program, contact:
Richard Dumas, Pesticide Re-Evaluation
Division (7508P), Office of Pesticide
Programs, Environmental Protection
Agency, 1200 Pennsylvania Ave. NW.,
Washington, DC 20460–0001; telephone
number: (703) 308–8015; email address:
dumas.richard@epa.gov.
SUPPLEMENTARY INFORMATION:
I. General Information
A. Does this action apply to me?
This action is directed to the public
in general and may be of interest to a
wide range of stakeholders including
environmental, human health, farm
worker, and agricultural advocates; the
chemical industry; pesticide users; and
members of the public interested in the
sale, distribution, or use of pesticides.
Since others also may be interested, the
Agency has not attempted to describe all
the specific entities that may be affected
by this action. If you have any questions
regarding the applicability of this action
to a particular entity, consult the
Chemical Review Manager listed in
Table 1 of Unit III.
B. What should I consider as I prepare
my comments for EPA?
1. Submitting CBI. Do not submit this
information to EPA through
regulations.gov or email. Clearly mark
the part or all of the information that
you claim to be CBI. For CBI
information in a disk or CD–ROM that
you mail to EPA, mark the outside of the
disk or CD–ROM as CBI and then
identify electronically within the disk or
CD–ROM the specific information that
is claimed as CBI. In addition to one
complete version of the comment that
includes information claimed as CBI, a
copy of the comment that does not
contain the information claimed as CBI
must be submitted for inclusion in the
public docket. Information so marked
will not be disclosed except in
accordance with procedures set forth in
40 CFR part 2.
2. Tips for preparing your comments.
When preparing and submitting your
comments, see the commenting tips at
https://www.epa.gov/dockets/
comments.html.
3. Environmental justice. EPA seeks to
achieve environmental justice, the fair
treatment and meaningful involvement
of any group, including minority and/or
low income populations, in the
development, implementation, and
enforcement of environmental laws,
regulations, and policies. To help
address potential environmental justice
24611
issues, the Agency seeks information on
any groups or segments of the
population who, as a result of their
location, cultural practices, or other
factors, may have atypical or
disproportionately high and adverse
human health impacts or environmental
effects from exposure to the pesticides
discussed in this document, compared
to the general population.
II. Authority
EPA is conducting its registration
review of aldicarb, bensulide,
coumaphos, ethalfluralin, and
pirimiphos-methyl pursuant to section
3(g) of the Federal Insecticide,
Fungicide, and Rodenticide Act (FIFRA)
and the Procedural Regulations for
Registration Review at 40 CFR part 155,
subpart C. Section 3(g) of FIFRA
provides, among other things, that the
registrations of pesticides are to be
reviewed every 15 years. Under FIFRA,
a pesticide product may be registered or
remain registered only if it meets the
statutory standard for registration given
in FIFRA section 3(c)(5) (7 U.S.C.
136a(c)(5)). When used in accordance
with widespread and commonly
recognized practice, the pesticide
product must perform its intended
function without unreasonable adverse
effects on the environment; that is,
without any unreasonable risk to man or
the environment, or a human dietary
risk from residues that result from the
use of a pesticide in or on food.
III. Registration Reviews
As directed by FIFRA section 3(g),
EPA is reviewing the pesticide
registration for aldicarb, bensulide,
coumaphos, ethalfluralin, and
pirimiphos-methyl to ensure that it
continues to satisfy the FIFRA standard
for registration—that is, that aldicarb,
bensulide, coumaphos, ethalfluralin,
and pirimiphos-methyl can still be used
without unreasonable adverse effects on
human health or the environment.
TABLE 1—DRAFT RISK ASSESSMENTS BEING MADE AVAILABLE FOR PUBLIC COMMENT
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Registration review case name
and number
Docket ID number
Aldicarb .......................................................
0140
Bensulide ....................................................
2035
Coumaphos ................................................
0018
Ethalfluralin .................................................
2260
Pirimiphos-methyl .......................................
2535
EPA–HQ–OPP–2012–0161
Susan Bartow, bartow.susan@epa.gov, (703) 603–0065.
EPA–HQ–OPP–2008–0022
Margaret Hathaway, hathaway.margaret@epa.gov, (703) 305–5076.
EPA–HQ–OPP–2008–0023
Brian Kettl, kettl.brian@epa.gov, (703) 347–0535.
EPA–HQ–OPP–2011–0094
Kelly Ballard, ballard.kelly@epa.gov, (703) 305–8126.
EPA–HQ–OPP–2009–0056
Caitlin Newcamp, newcamp.caitlin@epa.gov, (703) 347–0397.
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Chemical review manager and contact information
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Aldicarb. Draft Human Health and
Ecological Risk Assessments (EPA–HQ–
OPP–2012–0161). Aldicarb is a systemic
carbamate insecticide, acaricide, and
nematicide registered for use on cotton,
dry beans, peanuts, soybeans, sugar
beets, and sweet potatoes. It is not
registered for non-agricultural/
residential use. EPA conducted a
comprehensive human health risk
assessment including a highly refined
acute dietary exposure assessment for
all existing food uses of aldicarb. Acute
dietary exposure estimates for drinking
water as well as food and drinking water
combined are of concern. A commodity
specific analysis (CSA) was conducted
to obtain estimates of acute exposure
and risk following a single consumption
of a single commodity. Exposure
estimates were above the level of
concern for children following
consumption of sweet potatoes or
potatoes. Additionally, there are shortand intermediate-term occupational
handler risk estimates of concern for the
registered uses of aldicarb with labelspecified personal protective
equipment. EPA also conducted a
screening level ecological risk
assessment and identified potential
risks to both aquatic and terrestrial nontarget organisms. The assessments did
not cover the EDSP component of this
registration review case, nor does it
include a full pollinator assessment or
a complete endangered species
assessment.
Bensulide. Draft Human Health and
Ecological Risk Assessments (EPA–HQ–
OPP–2008–0022). Bensulide is a
systemic organophosphate herbicide
registered to control grasses and
broadleaf weeds in a variety of
agricultural (e.g., lettuce, cantaloupe,
broccoli) and non-agricultural (golf
course, turf farm, residential lawn,
rights-of-way, and landscaping) settings,
and is usually applied to bare ground
before crops are planted. EPA
conducted a comprehensive human
health risk assessment and identified
risks of concern for dietary, residential,
occupational, and spray drift exposures.
The bensulide risk assessment retained
the FQPA 10x safety factor due to the
uncertainty in the human dose-response
relationship for neuro-developmental
effects. EPA also conducted an
ecological risk assessment for bensulide,
which identified risks of concern for
non-listed species for birds, reptiles,
and terrestrial-phase amphibians;
mammals; freshwater fish and aquaticphase amphibians; marine/estuarine
fish; freshwater invertebrates; and
aquatic vascular plants. Neither an
endangered species assessment nor a
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pollinator assessment been completed
for bensulide at this time. Bensulide is
on the second list of chemicals for tier
one screening under the Endocrine
Disruptor Screening Program (EDSP).
Coumaphos. Draft Human Health and
Ecological Risk Assessments (EPA–HQ–
OPP–2008–0023). Coumaphos is an
organophosphate acaricide. It is used to
control ticks and mites on livestock, as
well as to control varroa mites and small
hive beetles in beehives. The human
health risk assessment for coumaphos
found dietary risks of concern, with
food (beef meat) being the driver in the
steady state risk estimates. In addition,
almost all of the occupational exposure
scenarios show risks of concern for both
dermal and inhalation routes of
exposure at varying levels of personal
protection equipment and all
formulations with the exception of
liquid. The coumaphos risk assessment
retained the FQPA 10x safety factor due
to the uncertainty in human doseresponse relationship for neurodevelopmental effects. Coumaphos is
expected to pose an acute risk to birds.
Coumaphos is not expected to pose a
risk to endangered or non-endangered
mammals because of its limited use
pattern. Coumaphos usage on cattle may
pose a high acute risk to aquatic
invertebrates. Coumaphos is not
expected to pose chronic or acute risks
to listed or non-listed fish. Neither a
comprehensive endangered species
assessment nor a pollinator assessment
has been completed for coumaphos at
this time. Coumaphos is on the second
list of chemicals for Tier 1 screening
under EDSP.
Ethalfluralin. Draft Human Health
and Ecological Risk Assessments (EPA–
HQ–OPP–2011–0094). Ethalfluralin is a
preemergence herbicide used to control
a variety of annual grasses and broadleaf
weeds on agricultural sites. Ethalfluralin
has multiple end-use products that are
registered for use on various agricultural
crops. EPA conducted a comprehensive
human health risk assessment and did
not identify any risks of concern. EPA
also conducted an ecological risk
assessment. Potential risks to aquatic
animals, aquatic and terrestrial plants,
and mammals were identified. The
assessments did not cover the EDSP
component of this registration review
case, nor does it include either a full
pollinator assessment or a complete
endangered species assessment.
Pirimiphos-methyl. Draft Human
Health Risk and Ecological Assessments
(EPA–HQ–OPP–2009–0056).
Pirimiphos-methyl is a member of the
organophosphate class of pesticides.
Currently, it is registered for use as an
insecticide in cattle ear tags, and on
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post-harvest stored grain/seeds
(sorghum and corn). There are two
special local need FIFRA section 24(c)
registrations: A fogger treatment on iris
bulbs in Washington, and a fogger and
drench treatment on gladiola bulbs in
Michigan. EPA conducted a human
health risk assessment, and did not
identify any risks of concern for dietary
or residential exposures. However, risks
of concern were identified for
occupational exposure and for all
handler scenarios. The pirimiphosmethyl risk assessment retained the
FQPA 10x safety factor due to the
uncertainty in human dose-response
relationship for neuro-developmental
effects. EPA also conducted a
quantitative ecological risk assessment
and identified potential risks to
terrestrial and aquatic invertebrates. A
complete endangered species
assessment nor a pollinator assessment
has been completed for pirimiphosmethyl. The assessments did not cover
the EDSP component of this registration
review case.
Pursuant to 40 CFR 155.53(c), EPA is
providing an opportunity, through this
notice of availability, for interested
parties to provide comments and input
concerning the Agency’s draft human
health and ecological risk assessments
for aldicarb, bensulide, coumaphos,
ethalfluralin, and pirimiphos-methyl.
Such comments and input could
address, among other things, the
Agency’s risk assessment methodologies
and assumptions, as applied to this draft
risk assessment. The Agency will
consider all comments received during
the public comment period and make
changes, as appropriate, to the draft
human health and ecological risk
assessments. EPA will then issue a
revised risk assessment, explain any
changes to the draft risk assessment, and
respond to comments. In the Federal
Register notice announcing the
availability of the revised risk
assessment, if the revised risk
assessment indicates risks of concern,
the Agency may provide a comment
period for the public to submit
suggestions for mitigating the risk
identified in the revised risk assessment
before developing a proposed
registration review decision on aldicarb,
bensulide, coumaphos, ethalfluralin,
and pirimiphos-methyl.
1. Other related information.
Additional information on aldicarb,
bensulide, coumaphos, ethalfluralin,
and pirimiphos-methyl is available on
the Agency’s registration review
program and its implementing
regulation is available at https://
www.epa.gov/pesticide-reevaluation.
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2. Information submission
requirements. Anyone may submit data
or information in response to this
document. To be considered during a
pesticide’s registration review, the
submitted data or information must
meet the following requirements:
• To ensure that EPA will consider
data or information submitted,
interested persons must submit the data
or information during the comment
period. The Agency may, at its
discretion, consider data or information
submitted at a later date.
• The data or information submitted
must be presented in a legible and
useable form. For example, an English
translation must accompany any
material that is not in English and a
written transcript must accompany any
information submitted as an
audiographic or videographic record.
Written material may be submitted in
paper or electronic form.
• Submitters must clearly identify the
source of any submitted data or
information.
• Submitters may request the Agency
to reconsider data or information that
the Agency rejected in a previous
review. However, submitters must
explain why they believe the Agency
should reconsider the data or
information in the pesticide’s
registration review.
As provided in 40 CFR 155.58, the
registration review docket for each
pesticide case will remain publicly
accessible through the duration of the
registration review process; that is, until
all actions required in the final decision
on the registration review case have
been completed.
Authority: 7 U.S.C. 136 et seq.
Dated: March 14, 2016.
Yu-Ting Guilaran,
Director, Pesticide Re-Evaluation Division,
Office of Pesticide Programs.
[FR Doc. 2016–09732 Filed 4–25–16; 8:45 am]
BILLING CODE 6560–50–P
FEDERAL RESERVE SYSTEM
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Formations of, Acquisitions by, and
Mergers of Bank Holding Companies
The companies listed in this notice
have applied to the Board for approval,
pursuant to the Bank Holding Company
Act of 1956 (12 U.S.C. 1841 et seq.)
(BHC Act), Regulation Y (12 CFR part
225), and all other applicable statutes
and regulations to become a bank
holding company and/or to acquire the
assets or the ownership of, control of, or
the power to vote shares of a bank or
bank holding company and all of the
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22:08 Apr 25, 2016
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banks and nonbanking companies
owned by the bank holding company,
including the companies listed below.
The applications listed below, as well
as other related filings required by the
Board, are available for immediate
inspection at the Federal Reserve Bank
indicated. The applications will also be
available for inspection at the offices of
the Board of Governors. Interested
persons may express their views in
writing on the standards enumerated in
the BHC Act (12 U.S.C. 1842(c)). If the
proposal also involves the acquisition of
a nonbanking company, the review also
includes whether the acquisition of the
nonbanking company complies with the
standards in section 4 of the BHC Act
(12 U.S.C. 1843). Unless otherwise
noted, nonbanking activities will be
conducted throughout the United States.
Unless otherwise noted, comments
regarding each of these applications
must be received at the Reserve Bank
indicated or the offices of the Board of
Governors not later than May 20, 2016.
A. Federal Reserve Bank of Atlanta
(Chapelle Davis, Assistant Vice
President) 1000 Peachtree Street NE.,
Atlanta, Georgia 30309. Comments can
also be sent electronically to
Applications.Comments@atl.frb.org:
1. United Community Banks, Inc.,
Blairsville, Georgia; to merge with
Tidelands Bancshares, Inc., and thereby
acquire Tidelands Bank, both of Mt.
Pleasant, South Carolina.
B. Federal Reserve Bank of St. Louis
(David L. Hubbard, Senior Manager)
P.O. Box 442, St. Louis, Missouri
63166–2034. Comments can also be sent
electronically to
Comments.applications@stls.frb.org:
1. Stupp Bros., Inc., and Midwest
BankCentre, Inc., both of St. Louis,
Missouri, to indirectly acquire 100
percent of the voting shares of Bremen
Bancorp, Inc., and thereby indirectly
acquire Bremen Bank and Trust
Company, both in St Louis, Missouri.
Board of Governors of the Federal Reserve
System, April 21, 2016.
Michael J. Lewandowski,
Associate Secretary of the Board.
[FR Doc. 2016–09634 Filed 4–25–16; 8:45 am]
BILLING CODE 6210–01–P
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DEPARTMENT OF DEFENSE
GENERAL SERVICES
ADMINISTRATION
NATIONAL AERONAUTICS AND
SPACE ADMINISTRATION
[OMB Control No. 9000–0145]; [Docket
2016–0053; Sequence 7]
Submission for OMB Review; Use of
Data Universal Numbering System
(DUNS) as Primary Contractor
Identification
Department of Defense (DOD),
General Services Administration (GSA),
and National Aeronautics and Space
Administration (NASA).
ACTION: Notice of request for public
comments regarding an extension to an
existing OMB clearance.
AGENCY:
Under the provisions of the
Paperwork Reduction Act Regulatory
Secretariat Division will be submitting
to the Office of Management and Budget
(OMB) a request to review and approve
an extension of a previously approved
information collection requirement
concerning use of the Data Universal
Numbering System (DUNS) as primary
contractor identification. The DUNS
number is the nine-digit identification
number assigned by Dun and Bradstreet
Information Services to an
establishment. A notice was published
in the Federal Register at 81 FR 6860 on
February 9, 2016. Two respondents
submitted eight comments that were
received.
SUMMARY:
Submit comments on or before
May 26, 2016.
ADDRESSES: Submit comments regarding
this burden estimate or any other aspect
of this collection of information,
including suggestions for reducing this
burden to: Office of Information and
Regulatory Affairs of OMB, Attention:
Desk Officer for GSA, Room 10236,
NEOB, Washington, DC 20503.
Additionally submit a copy to GSA by
any of the following methods:
• Regulations.gov: https://
www.regulations.gov. Submit comments
via the Federal eRulemaking portal by
searching the OMB control number.
Select the link ‘‘Submit a Comment’’
that corresponds with ‘‘Information
Collection 9000–0145, Use of Data
Universal Numbering System (DUNS) as
Primary Contractor Identification’’.
Follow the instructions provided at the
‘‘Submit a Comment’’ screen. Please
include your name, company name (if
any), and ‘‘Information Collection 9000–
0145, Use of Data Universal Numbering
System (DUNS) as Primary Contractor
DATES:
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26APN1
Agencies
[Federal Register Volume 81, Number 80 (Tuesday, April 26, 2016)]
[Notices]
[Pages 24610-24613]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2016-09732]
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ENVIRONMENTAL PROTECTION AGENCY
[EPA-HQ-OPP-2015-0794; FRL-9943-82]
Aldicarb, Bensulide, Coumaphos, Ethalfluralin, and Pirimiphos-
methyl Registration Review; Draft Human Health and Ecological Risk
Assessments; Notice of Availability
AGENCY: Environmental Protection Agency (EPA).
ACTION: Notice.
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SUMMARY: This notice announces the availability of EPA's draft human
health risk and draft ecological risk assessments for aldicarb,
bensulide, coumaphos, ethalfluralin, and pirimiphos-methyl and opens a
public comment period on these documents. Registration review is EPA's
periodic review of pesticide registrations to ensure that each
pesticide continues to satisfy the statutory standard for registration,
that is, the pesticide can perform its intended function without
unreasonable adverse effects on human health or the environment. As
part of the registration review process, the Agency has completed a
comprehensive draft human health and ecological risk assessments for
all aldicarb, bensulide, coumaphos, ethalfluralin, and pirimiphos-
methyl uses. After reviewing comments received during the public
comment period, EPA will issue a revised risk assessment, explain any
changes to the draft risk assessment, and respond to comments and may
request public input on risk mitigation before completing a proposed
registration review decision for aldicarb, bensulide, coumaphos,
ethalfluralin, and pirimiphos-methyl. Through this program, EPA is
ensuring that each pesticide's registration is based on
[[Page 24611]]
current scientific and other knowledge, including its effects on human
health and the environment.
DATES: Comments must be received on or before June 27, 2016.
ADDRESSES: Submit your comments, identified by docket identification
(ID) number EPA-HQ-OPP-2015-0794, 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 Confidential Business
Information (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.
FOR FURTHER INFORMATION CONTACT: For pesticide specific information
contact: The Chemical Review Manager listed in Table 1of Unit III.
For general questions on the registration review program, contact:
Richard Dumas, Pesticide Re-Evaluation Division (7508P), Office of
Pesticide Programs, Environmental Protection Agency, 1200 Pennsylvania
Ave. NW., Washington, DC 20460-0001; telephone number: (703) 308-8015;
email address: dumas.richard@epa.gov.
SUPPLEMENTARY INFORMATION:
I. General Information
A. Does this action apply to me?
This action is directed to the public in general and may be of
interest to a wide range of stakeholders including environmental, human
health, farm worker, and agricultural advocates; the chemical industry;
pesticide users; and members of the public interested in the sale,
distribution, or use of pesticides. Since others also may be
interested, the Agency has not attempted to describe all the specific
entities that may be affected by this action. If you have any questions
regarding the applicability of this action to a particular entity,
consult the Chemical Review Manager listed in Table 1 of Unit III.
B. What should I consider as I prepare my comments for EPA?
1. Submitting CBI. Do not submit this information to EPA through
regulations.gov or email. Clearly mark the part or all of the
information that you claim to be CBI. For CBI information in a disk or
CD-ROM that you mail to EPA, mark the outside of the disk or CD-ROM as
CBI and then identify electronically within the disk or CD-ROM the
specific information that is claimed as CBI. In addition to one
complete version of the comment that includes information claimed as
CBI, a copy of the comment that does not contain the information
claimed as CBI must be submitted for inclusion in the public docket.
Information so marked will not be disclosed except in accordance with
procedures set forth in 40 CFR part 2.
2. Tips for preparing your comments. When preparing and submitting
your comments, see the commenting tips at https://www.epa.gov/dockets/comments.html.
3. Environmental justice. EPA seeks to achieve environmental
justice, the fair treatment and meaningful involvement of any group,
including minority and/or low income populations, in the development,
implementation, and enforcement of environmental laws, regulations, and
policies. To help address potential environmental justice issues, the
Agency seeks information on any groups or segments of the population
who, as a result of their location, cultural practices, or other
factors, may have atypical or disproportionately high and adverse human
health impacts or environmental effects from exposure to the pesticides
discussed in this document, compared to the general population.
II. Authority
EPA is conducting its registration review of aldicarb, bensulide,
coumaphos, ethalfluralin, and pirimiphos-methyl pursuant to section
3(g) of the Federal Insecticide, Fungicide, and Rodenticide Act (FIFRA)
and the Procedural Regulations for Registration Review at 40 CFR part
155, subpart C. Section 3(g) of FIFRA provides, among other things,
that the registrations of pesticides are to be reviewed every 15 years.
Under FIFRA, a pesticide product may be registered or remain registered
only if it meets the statutory standard for registration given in FIFRA
section 3(c)(5) (7 U.S.C. 136a(c)(5)). When used in accordance with
widespread and commonly recognized practice, the pesticide product must
perform its intended function without unreasonable adverse effects on
the environment; that is, without any unreasonable risk to man or the
environment, or a human dietary risk from residues that result from the
use of a pesticide in or on food.
III. Registration Reviews
As directed by FIFRA section 3(g), EPA is reviewing the pesticide
registration for aldicarb, bensulide, coumaphos, ethalfluralin, and
pirimiphos-methyl to ensure that it continues to satisfy the FIFRA
standard for registration--that is, that aldicarb, bensulide,
coumaphos, ethalfluralin, and pirimiphos-methyl can still be used
without unreasonable adverse effects on human health or the
environment.
Table 1--Draft Risk Assessments Being Made Available for Public Comment
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Registration review case name and Chemical review manager and
number Docket ID number contact information
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Aldicarb............................ EPA-HQ-OPP-2012-0161 Susan Bartow,
0140................................ bartow.susan@epa.gov, (703) 603-
0065.
Bensulide........................... EPA-HQ-OPP-2008-0022 Margaret Hathaway,
2035................................ hathaway.margaret@epa.gov,
(703) 305-5076.
Coumaphos........................... EPA-HQ-OPP-2008-0023 Brian Kettl,
0018................................ kettl.brian@epa.gov, (703) 347-
0535.
Ethalfluralin....................... EPA-HQ-OPP-2011-0094 Kelly Ballard,
2260................................ ballard.kelly@epa.gov, (703)
305-8126.
Pirimiphos-methyl................... EPA-HQ-OPP-2009-0056 Caitlin Newcamp,
2535................................ newcamp.caitlin@epa.gov, (703)
347-0397.
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[[Page 24612]]
Aldicarb. Draft Human Health and Ecological Risk Assessments (EPA-
HQ-OPP-2012-0161). Aldicarb is a systemic carbamate insecticide,
acaricide, and nematicide registered for use on cotton, dry beans,
peanuts, soybeans, sugar beets, and sweet potatoes. It is not
registered for non-agricultural/residential use. EPA conducted a
comprehensive human health risk assessment including a highly refined
acute dietary exposure assessment for all existing food uses of
aldicarb. Acute dietary exposure estimates for drinking water as well
as food and drinking water combined are of concern. A commodity
specific analysis (CSA) was conducted to obtain estimates of acute
exposure and risk following a single consumption of a single commodity.
Exposure estimates were above the level of concern for children
following consumption of sweet potatoes or potatoes. Additionally,
there are short- and intermediate-term occupational handler risk
estimates of concern for the registered uses of aldicarb with label-
specified personal protective equipment. EPA also conducted a screening
level ecological risk assessment and identified potential risks to both
aquatic and terrestrial non-target organisms. The assessments did not
cover the EDSP component of this registration review case, nor does it
include a full pollinator assessment or a complete endangered species
assessment.
Bensulide. Draft Human Health and Ecological Risk Assessments (EPA-
HQ-OPP-2008-0022). Bensulide is a systemic organophosphate herbicide
registered to control grasses and broadleaf weeds in a variety of
agricultural (e.g., lettuce, cantaloupe, broccoli) and non-agricultural
(golf course, turf farm, residential lawn, rights-of-way, and
landscaping) settings, and is usually applied to bare ground before
crops are planted. EPA conducted a comprehensive human health risk
assessment and identified risks of concern for dietary, residential,
occupational, and spray drift exposures. The bensulide risk assessment
retained the FQPA 10x safety factor due to the uncertainty in the human
dose-response relationship for neuro-developmental effects. EPA also
conducted an ecological risk assessment for bensulide, which identified
risks of concern for non-listed species for birds, reptiles, and
terrestrial-phase amphibians; mammals; freshwater fish and aquatic-
phase amphibians; marine/estuarine fish; freshwater invertebrates; and
aquatic vascular plants. Neither an endangered species assessment nor a
pollinator assessment been completed for bensulide at this time.
Bensulide is on the second list of chemicals for tier one screening
under the Endocrine Disruptor Screening Program (EDSP).
Coumaphos. Draft Human Health and Ecological Risk Assessments (EPA-
HQ-OPP-2008-0023). Coumaphos is an organophosphate acaricide. It is
used to control ticks and mites on livestock, as well as to control
varroa mites and small hive beetles in beehives. The human health risk
assessment for coumaphos found dietary risks of concern, with food
(beef meat) being the driver in the steady state risk estimates. In
addition, almost all of the occupational exposure scenarios show risks
of concern for both dermal and inhalation routes of exposure at varying
levels of personal protection equipment and all formulations with the
exception of liquid. The coumaphos risk assessment retained the FQPA
10x safety factor due to the uncertainty in human dose-response
relationship for neuro-developmental effects. Coumaphos is expected to
pose an acute risk to birds. Coumaphos is not expected to pose a risk
to endangered or non-endangered mammals because of its limited use
pattern. Coumaphos usage on cattle may pose a high acute risk to
aquatic invertebrates. Coumaphos is not expected to pose chronic or
acute risks to listed or non-listed fish. Neither a comprehensive
endangered species assessment nor a pollinator assessment has been
completed for coumaphos at this time. Coumaphos is on the second list
of chemicals for Tier 1 screening under EDSP.
Ethalfluralin. Draft Human Health and Ecological Risk Assessments
(EPA-HQ-OPP-2011-0094). Ethalfluralin is a preemergence herbicide used
to control a variety of annual grasses and broadleaf weeds on
agricultural sites. Ethalfluralin has multiple end-use products that
are registered for use on various agricultural crops. EPA conducted a
comprehensive human health risk assessment and did not identify any
risks of concern. EPA also conducted an ecological risk assessment.
Potential risks to aquatic animals, aquatic and terrestrial plants, and
mammals were identified. The assessments did not cover the EDSP
component of this registration review case, nor does it include either
a full pollinator assessment or a complete endangered species
assessment.
Pirimiphos-methyl. Draft Human Health Risk and Ecological
Assessments (EPA-HQ-OPP-2009-0056). Pirimiphos-methyl is a member of
the organophosphate class of pesticides. Currently, it is registered
for use as an insecticide in cattle ear tags, and on post-harvest
stored grain/seeds (sorghum and corn). There are two special local need
FIFRA section 24(c) registrations: A fogger treatment on iris bulbs in
Washington, and a fogger and drench treatment on gladiola bulbs in
Michigan. EPA conducted a human health risk assessment, and did not
identify any risks of concern for dietary or residential exposures.
However, risks of concern were identified for occupational exposure and
for all handler scenarios. The pirimiphos-methyl risk assessment
retained the FQPA 10x safety factor due to the uncertainty in human
dose-response relationship for neuro-developmental effects. EPA also
conducted a quantitative ecological risk assessment and identified
potential risks to terrestrial and aquatic invertebrates. A complete
endangered species assessment nor a pollinator assessment has been
completed for pirimiphos-methyl. The assessments did not cover the EDSP
component of this registration review case.
Pursuant to 40 CFR 155.53(c), EPA is providing an opportunity,
through this notice of availability, for interested parties to provide
comments and input concerning the Agency's draft human health and
ecological risk assessments for aldicarb, bensulide, coumaphos,
ethalfluralin, and pirimiphos-methyl. Such comments and input could
address, among other things, the Agency's risk assessment methodologies
and assumptions, as applied to this draft risk assessment. The Agency
will consider all comments received during the public comment period
and make changes, as appropriate, to the draft human health and
ecological risk assessments. EPA will then issue a revised risk
assessment, explain any changes to the draft risk assessment, and
respond to comments. In the Federal Register notice announcing the
availability of the revised risk assessment, if the revised risk
assessment indicates risks of concern, the Agency may provide a comment
period for the public to submit suggestions for mitigating the risk
identified in the revised risk assessment before developing a proposed
registration review decision on aldicarb, bensulide, coumaphos,
ethalfluralin, and pirimiphos-methyl.
1. Other related information. Additional information on aldicarb,
bensulide, coumaphos, ethalfluralin, and pirimiphos-methyl is available
on the Agency's registration review program and its implementing
regulation is available at https://www.epa.gov/pesticide-reevaluation.
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2. Information submission requirements. Anyone may submit data or
information in response to this document. To be considered during a
pesticide's registration review, the submitted data or information must
meet the following requirements:
To ensure that EPA will consider data or information
submitted, interested persons must submit the data or information
during the comment period. The Agency may, at its discretion, consider
data or information submitted at a later date.
The data or information submitted must be presented in a
legible and useable form. For example, an English translation must
accompany any material that is not in English and a written transcript
must accompany any information submitted as an audiographic or
videographic record. Written material may be submitted in paper or
electronic form.
Submitters must clearly identify the source of any
submitted data or information.
Submitters may request the Agency to reconsider data or
information that the Agency rejected in a previous review. However,
submitters must explain why they believe the Agency should reconsider
the data or information in the pesticide's registration review.
As provided in 40 CFR 155.58, the registration review docket for
each pesticide case will remain publicly accessible through the
duration of the registration review process; that is, until all actions
required in the final decision on the registration review case have
been completed.
Authority: 7 U.S.C. 136 et seq.
Dated: March 14, 2016.
Yu-Ting Guilaran,
Director, Pesticide Re-Evaluation Division, Office of Pesticide
Programs.
[FR Doc. 2016-09732 Filed 4-25-16; 8:45 am]
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