Registration Review; Draft Human Health and Ecological Risk Assessments; Notice of Availability, 478-481 [2015-33298]
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478
Federal Register / Vol. 81, No. 3 / Wednesday, January 6, 2016 / Notices
Description: Market-Based Triennial
Review Filing: Roosevelt Wind Project
Triennial Filing to be effective 2/28/
2016.
Filed Date: 12/29/15.
Accession Number: 20151229–5285.
Comments Due: 5 p.m. ET 2/29/16.
Docket Numbers: ER16–653–000.
Applicants: Slate Creek Wind Project,
LLC.
Description: Market-Based Triennial
Review Filing: Slate Creek Wind
Triennial Filing to be effective 2/28/
2016.
Filed Date: 12/29/15.
Accession Number: 20151229–5286.
Comments Due: 5 p.m. ET 2/29/16.
Docket Numbers: ER16–654–000.
Applicants: Spearville 3, LLC.
Description: Market-Based Triennial
Review Filing: Spearville 3 Triennial
Filing to be effective 2/28/2016.
Filed Date: 12/29/15.
Accession Number: 20151229–5289.
Comments Due: 5 p.m. ET 2/29/16.
Docket Numbers: ER16–655–000.
Applicants: Spinning Spur Wind LLC.
Description: Market-Based Triennial
Review Filing: Spinning Spur Wind
Triennial Filing to be effective 2/28/
2016.
Filed Date: 12/29/15.
Accession Number: 20151229–5290.
Comments Due: 5 p.m. ET 2/29/16.
Docket Numbers: ER16–656–000.
Applicants: Oasis Power Partners,
LLC.
Description: Market-Based Triennial
Review Filing: Oasis Power Partners
Triennial Update to be effective 2/28/
2016.
Filed Date: 12/29/15.
Accession Number: 20151229–5291.
Comments Due: 5 p.m. ET 2/29/16.
Docket Numbers: ER16–657–000.
Applicants: Pacific Wind Lessee, LLC.
Description: Market-Based Triennial
Review Filing: Pacific Wind Lessee
Triennial Filing to be effective 2/28/
2016.
Filed Date: 12/29/15.
Accession Number: 20151229–5292.
Comments Due: 5 p.m. ET 2/29/16.
Docket Numbers: ER16–658–000.
Applicants: Shiloh Wind Project 2,
LLC.
Description: Market-Based Triennial
Review Filing: Shiloh Wind Project 2
Triennial Filing to be effective 2/28/
2016.
Filed Date: 12/29/15.
Accession Number: 20151229–5293.
Comments Due: 5 p.m. ET 2/29/16.
Docket Numbers: ER16–659–000.
Applicants: Shiloh III Lessee, LLC.
Description: Market-Based Triennial
Review Filing: Shiloh III Lessee
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Triennial Filing to be effective 2/28/
2016.
Filed Date: 12/29/15.
Accession Number: 20151229–5294.
Comments Due: 5 p.m. ET 2/29/16.
Docket Numbers: ER16–660–000.
Applicants: Shiloh IV Lessee, LLC.
Description: Market-Based Triennial
Review Filing: Shiloh IV Lessee
Triennial Filing to be effective 2/28/
2016.
Filed Date: 12/29/15.
Accession Number: 20151229–5295.
Comments Due: 5 p.m. ET 2/29/16.
Docket Numbers: ER16–661–000.
Applicants: Appalachian Power
Company.
Description: Section 205(d) Rate
Filing: OATT—Revise Attachment K,
TCC and TNC Rate Update to be
effective 12/31/9998.
Filed Date: 12/29/15.
Accession Number: 20151229–5304.
Comments Due: 5 p.m. ET 1/19/16.
Docket Numbers: ER16–662–000.
Applicants: Duke Energy Progress,
LLC.
Description: Tariff Cancellation: DEP
Cancellation Filing to be effective 2/28/
2016.
Filed Date: 12/30/15.
Accession Number: 20151230–5017.
Comments Due: 5 p.m. ET 1/20/16.
Docket Numbers: ER16–663–000.
Applicants: Duke Energy Florida,
LLC.
Description: Tariff Cancellation: DEF
Cancellation Filing to be effective 2/28/
2016.
Filed Date: 12/30/15.
Accession Number: 20151230–5018.
Comments Due: 5 p.m. ET 1/20/16.
Docket Numbers: ER16–664–000.
Applicants: Midcontinent
Independent System Operator, Inc.,
Entergy Services, Inc.
Description: Section 205(d) Rate
Filing: 2015–12–30_RS 40 Revised EMI–
SMEPA JPZ to be effective 1/1/2016.
Filed Date: 12/30/15.
Accession Number: 20151230–5108
Comments Due: 5 p.m. ET 1/20/16.
The filings are accessible in the
Commission’s eLibrary system by
clicking on the links or querying the
docket number.
Any person desiring to intervene or
protest in any of the above proceedings
must file in accordance with Rules 211
and 214 of the Commission’s
Regulations (18 CFR 385.211 and
385.214) on or before 5:00 p.m. Eastern
time on the specified comment date.
Protests may be considered, but
intervention is necessary to become a
party to the proceeding.
eFiling is encouraged. More detailed
information relating to filing
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requirements, interventions, protests,
service, and qualifying facilities filings
can be found at: https://www.ferc.gov/
docs-filing/efiling/filing-req.pdf. For
other information, call (866) 208–3676
(toll free). For TTY, call (202) 502–8659.
Dated: December 30, 2015.
Nathaniel J. Davis, Sr.,
Deputy Secretary.
[FR Doc. 2015–33223 Filed 1–5–16; 8:45 am]
BILLING CODE 6717–01–P
ENVIRONMENTAL PROTECTION
AGENCY
[EPA–HQ–OPP–2015–0794; FRL–9940–41]
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
and ecological risk assessments for the
registration review of a group of
pesticides identified individually in this
document in the table in Unit III, and
opens a public comment period.
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
assessment for the identified pesticides.
After reviewing comments received
during the public comment period on
each assessment, EPA may issue revised
risk assessments and explain any
changes to the draft risk assessments,
and respond to substantive comments
on the risk assessments. EPA may also
request public input on risk mitigation
before completing a proposed
registration review decision for the
identified pesticides. Through this
program, EPA is ensuring that each
pesticide’s registration is based on
current scientific and other knowledge,
including its effects on human health
and the environment.
DATES: Comments must be received on
or before March 7, 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
SUMMARY:
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Federal Register / Vol. 81, No. 3 / Wednesday, January 6, 2016 / Notices
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/where-sendcomments-epa-dockets.
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 (CRM)
identified in the table in 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.
479
Since others may also 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 the
table in Unit III.
B. What should I consider as I prepare
my comments for EPA?
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
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/
commenting-epa-dockets#tips.
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
EPA is conducting its registration
review of these pesticides 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
registrations for the pesticides listed in
the table to ensure that they continue to
satisfy the FIFRA standard for
registration—that is, that these
pesticides can still be used without
unreasonable adverse effects on human
health or the environment.
TABLE—DRAFT RISK ASSESSMENTS BEING MADE AVAILABLE FOR PUBLIC COMMENT
Registration review case name and No.
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Azoxystrobin, 7020 .................................
Bensulfuron-methyl, 7216 .......................
Bifenazate, 7609 .....................................
Boric Acid and Sodium Borate Salts,
0024.
Ethephon, 0382 .......................................
Hymexazol, 7016 ....................................
Lithium hypochlorite, 3084 ......................
Pronamide, 0082 .....................................
Docket ID No.
EPA–HQ–OPP–2009–0835
EPA–HQ–OPP–2011–0663
EPA–HQ–OPP–2012–0633
EPA–HQ–OPP–2009–0306
......
......
......
......
Veronica Dutch, dutch.veronica@epa.gov, (703) 308–8585.
Moana Appleyard, appleyard.moana@epa.gov, (703) 308–8175.
Garland Waleko, waleko.garland@epa.gov, (703) 308–8049.
Moana Appleyard, appleyard.moana@epa.gov, (703) 308–8175.
EPA–HQ–OPP–2010–0098
EPA–HQ–OPP–2010–0127
EPA–HQ–OPP–2013–0606
EPA–HQ–OPP–2009–0326
......
......
......
......
Marquea D. King, king.marquea@epa.gov, (703) 305–7432.
Caitlin Newcamp, newcamp.caitlin@epa.gov, (703) 347–0325.
Donna Kamarei, kamarei.donna@epa.gov, (703) 347–0443.
Wilhelmena Livingston, livingston.wilhelmena@epa.gov, (703) 308–
8025.
Azoxystrobin. Draft Human Health
and Ecological Risk Assessments (EPA–
HQ–OPP–2009–0835). Azoxystrobin is a
systemic fungicide and antimicrobial
registered for use on a variety of
terrestrial food and feed crops,
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Chemical review manager and contact information
including vegetables, fruits and nuts;
terrestrial non-food crops, including turf
and ornamentals; and non-crop sites
including additives for the manufacture
of paint, rubber, paper products,
textiles, and adhesives. The Agency has
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conducted draft human health and
ecological risk assessments for the
conventional and antimicrobial uses of
azoxystrobin. A full endangered species
assessment has not been completed for
azoxystrobin at this time. For foliar
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applications, the ecological risk
assessment identifies risks of concern
for aquatic plants, freshwater fish,
aquatic invertebrates, and mammals. For
seed treatments, risks of concern are
identified for birds and mammals. The
conventional uses of azoxystrobin are
associated with inhalation risks of
concern for residential handlers and
some occupational post-application
scenarios even with maximum personal
protective equipment (PPE). The
antimicrobial uses of azoxystrobin are
not associated with ecological risks of
concern, but the human health risk
assessment identifies potential risks of
concern for residential and occupational
handlers. Azoxystrobin has not been
assessed under the endocrine disruptor
screening program (EDSP) or for risks to
pollinators.
Bensulfuron-methyl. Draft Human
Health Risk Assessment (EPA–HQ–
OPP–2011–0663). Bensulfuron-methyl
is a sulfonylurea herbicide that acts by
inhibiting acetolactate synthase.
Bensulfuron-methyl is registered for use
to control broadleaf weeds and sedges in
aquatic rice production. Tolerances
have been established for crayfish, rice,
and rice straw. There are no registered
residential uses of bensulfuron-methyl.
Bensulfuron- methyl was first registered
in 1989, and a Final Work Plan was
published in February 2012. The
ecological risks of bensulfuron-methyl
were assessed together with all other
sulfonylureas in the Preliminary
Ecological Risk Assessment for
Registration Review of 22 Sulfonylurea
Herbicides, published in September
2015. EPA conducted a human health
risk assessment and did not identify any
risks of concern for dietary, residential,
occupational, or aggregate exposure.
Bensulfuron-methyl was not on either
initial list of chemicals to be screened
under the EDSP, nor has an endangered
species or pollinator assessment been
conducted at this time.
Bifenazate. Draft Human Health and
Ecological Risk Assessments (EPA–HQ–
OPP–2012–0633). Bifenazate is a
selective carbazate miticide/insecticide
that is registered for use to control the
motile stage of mites in agricultural and
non-agricultural sites including on
bearing and non-bearing fruit and
vegetable crops, cotton, conifer
plantations, ornamentals, and in
greenhouses, as well as indoor and
outdoor residential, commercial,
institutional, and recreational areas. The
human health non-occupational drift
assessment was updated in registration
review for bifenazate and found no risks
of concern. In the recent June 2014, new
use assessment, all dietary, residential,
occupational, and aggregate risks were
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not of concern. In the ecological
assessment, chronic risks of concern
were identified for mammals and birds.
There are acute risks identified for listed
birds, freshwater fish, freshwater
invertebrates, and estuarine and marine
invertebrates. There is also potential
acute and chronic risk to terrestrial
invertebrates. Bifenazate was not on
either initial list of chemicals to be
screened under the EDSP, nor has an
endangered species or pollinator
assessment been conducted at this time.
Boric Acid and Sodium Borate Salts.
Draft Human Health and Ecological Risk
Assessments (EPA–HQ–OPP–2009–
0306). Boric acid and its sodium salts
are inorganic compounds with
registrations for use as active
ingredients in insecticides, acaricides,
herbicides, algaecides, fungicides, and
wood and material preservatives. In
small quantities, boron is an essential
nutrient for aquatic vertebrates and
invertebrates and plants. There is also
evidence that boron is essential or, if not
essential, beneficial in birds and
mammals, in small quantities. Boric
acid and its sodium salts are also
present as inert ingredients in pesticide
products and as ingredients in nonpesticide consumer products. The
Agency issued a Final Work Plan for
boric acid in October 2009. The
ecological risk assessment identifies
potential risks to terrestrial
invertebrates, birds, mammals, reptiles,
terrestrial-phase amphibians, aquatic
organisms, and terrestrial plants. For
birds and mammals, risk is primarily
associated with the granular
formulations and bait uses. For aquatic
organisms, risk is primarily associated
with discharge of swimming pool, hot
tub, and spa effluent directly to surface
waters, to storm drains, roadways, and
potentially from storage of treated wood.
For terrestrial plants, risk is primarily
associated with discharge of effluent
from swimming pools, hot tubs, and
spas. The human health risk assessment
did not identify risks of concern. Boric
acid was not on either initial list of
chemicals to be screened under the
EDSP, nor has an endangered species or
pollinator assessment been conducted at
this time.
Ethephon. Draft Human Health and
Ecological Risk Assessments (EPA–HQ–
OPP–2010–0098). Ethephon, 2chloroethylphosphonic acid, is an
organophosphonate plant growth
regulator intended to promote fruit
ripening, abscission, flower induction,
breaking of apical dominance
(inhibition of the growth of lateral buds
by the terminal bud of a shoot), and
other plant responses through the
release of ethylene gas, a natural plant
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hormone. EPA conducted a human
health risk assessment and identified
aggregate risks of concern for children
ages 1–2 years old. EPA also conducted
an ecological risk assessment and
identified potential risks to birds,
mammals, and non-target plants. A full
endangered species assessment has not
been completed for ethephon at this
time. At this time, ethephon has not
been evaluated for its potential to affect
endocrine systems in mammals and
wildlife, nor has an assessment of risks
to pollinators been conducted.
Hymexazol. Draft Human Health and
Ecological Risk Assessments (EPA–HQ–
OPP–2010–0127). Hymexazol is a
systemic fungicide for control of foliar
and soil-borne plant diseases. There is
only one existing registration as a
commercial seed treatment for sugar
beets. Hymexazol may be applied only
using commercial seed treatment
equipment. A Final Work Plan for
hymexazol was published by the
Agency in September 2010, and data
were then required in a generic data
call-in, dated October 2011. The reviews
of the required data have been
incorporated into the draft risk
assessments. The Draft Human Health
Risk Assessment identified no dietary
risks of concern but identified potential
risk to occupational workers
(individuals treating/mixing seed and
individuals doing multiple activities).
The Draft Ecological Risk Assessment
identified potential risks to mammals
and birds. Hymexazol was not on either
initial list of chemicals to be screened
under the EDSP, and a complete
endangered species assessment has not
been conducted at this time.
Lithium hypochlorite. Draft Ecological
Risk Assessment (EPA–HQ–OPP–2013–
0606). Lithium hypochlorite is an
algicide, disinfectant, and fungicide. Its
primary pesticidal use is to control
algae, bacteria, and mildew in
swimming pool water systems, hot tubs,
and spas. EPA conducted a qualitative
ecological risk assessment on the
swimming pool uses of lithium
hypochlorite as part of registration
review. EPA previously conducted
human health and ecological risk
assessments at the time of the
Reregistration Eligibility Decision (RED)
for lithium hypochlorite in 1993.
Lithium hypochlorite was not on either
initial list of chemicals to be screened
under the EDSP, and an endangered
species assessment has not been
conducted at this time.
Pronamide. Draft Human Health and
Ecological Risk Assessments (EPA–HQ–
OPP–2009–0326). Pronamide, also
called propyzamide, 3,5-dichloro-N(1,1-dimethyl-2-propynyl)benzamide, is
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a selective, systemic, pre-and postemergence herbicide registered for the
control of grasses and broadleaf weeds
in several food and feed crops as well
as woody ornamentals, Christmas trees,
grasses grown for seed or turf (sod), golf
course turf, recreational area turf, and
fallow land. EPA conducted a human
health risk assessment and did not
identify any risks of concern for dietary,
residential, occupational, or aggregate
exposure. EPA also conducted an
ecological risk assessment and
identified potential risks to birds,
mammals, and plants. An endangered
species and pollinator assessment has
not been completed for pronamide at
this time. Pronamide was evaluated for
its potential to affect endocrine systems
in mammals and wildlife and the results
of the Agency’s review are found in the
weight of evidence review in this
registration review docket.
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 the pesticides identified in this
document. 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 may 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 the
pesticides identified in this document.
1. Other related information.
Additional information on pesticides
identified in this document is available
on the Pesticide Registration Review
Status Web page. Information on the
Agency’s registration review program
and its implementing regulation is
available at https://www.epa.gov/
pesticide-reevaluation/registrationreview-process.
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
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17:32 Jan 05, 2016
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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: December 24, 2015.
Richard P. Keigwin, Jr.,
Director, Pesticide Re-Evaluation Division,
Office of Pesticide Programs.
[FR Doc. 2015–33298 Filed 1–5–16; 8:45 am]
BILLING CODE 6560–50–P
[EPA–HQ–OPP–2015–0393; FRL–9939–58]
Registration Review Interim Decisions;
Notice of Availability
Environmental Protection
Agency (EPA).
ACTION: Notice.
AGENCY:
This notice announces the
availability of EPA’s interim registration
review decision for the pesticides listed
in Unit II of this notice. 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, that the pesticide can perform its
intended function without causing
SUMMARY:
Frm 00023
Fmt 4703
unreasonable adverse effects to human
health or the environment. Through this
program, EPA is ensuring that each
pesticide’s registration is based on
current scientific and other knowledge,
including its effects on human health
and the environment.
For
pesticide specific information, contact
the Chemical Review Manager
identified in the table in Unit II for the
pesticide of interest.
For general information 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.
FOR FURTHER INFORMATION CONTACT:
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
pesticide specific contact person listed
under FOR FURTHER INFORMATION
CONTACT.
B. How can I get copies of this document
and other related information?
ENVIRONMENTAL PROTECTION
AGENCY
PO 00000
481
Sfmt 4703
The docket for this action, identified
by docket identification (ID) number
EPA–HQ–OPP–2015–0393, is available
at https://www.regulations.gov or at the
Office of Pesticide Programs Regulatory
Public Docket (OPP Docket) in the
Environmental Protection Agency
Docket Center (EPA/DC), West William
Jefferson Clinton Bldg., Rm. 3334, 1301
Constitution Ave. NW., Washington, DC
20460–0001. The Public Reading Room
is open from 8:30 a.m. to 4:30 p.m.,
Monday through Friday, excluding legal
holidays. The telephone number for the
Public Reading Room is (202) 566–1744,
and the telephone number for the OPP
Docket is (703) 305–5805. Please review
the visitor instructions and additional
information about the docket available
at https://www.epa.gov/dockets.
E:\FR\FM\06JAN1.SGM
06JAN1
Agencies
[Federal Register Volume 81, Number 3 (Wednesday, January 6, 2016)]
[Notices]
[Pages 478-481]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2015-33298]
=======================================================================
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ENVIRONMENTAL PROTECTION AGENCY
[EPA-HQ-OPP-2015-0794; FRL-9940-41]
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 and ecological risk assessments for the registration review of a
group of pesticides identified individually in this document in the
table in Unit III, and opens a public comment period. 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
assessment for the identified pesticides. After reviewing comments
received during the public comment period on each assessment, EPA may
issue revised risk assessments and explain any changes to the draft
risk assessments, and respond to substantive comments on the risk
assessments. EPA may also request public input on risk mitigation
before completing a proposed registration review decision for the
identified pesticides. Through this program, EPA is ensuring that each
pesticide's registration is based on current scientific and other
knowledge, including its effects on human health and the environment.
DATES: Comments must be received on or before March 7, 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
[[Page 479]]
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/where-send-comments-epa-dockets.
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 (CRM) identified in the table in
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 may also 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 the table in 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/commenting-epa-dockets#tips.
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 these pesticides
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
registrations for the pesticides listed in the table to ensure that
they continue to satisfy the FIFRA standard for registration--that is,
that these pesticides can still be used without unreasonable adverse
effects on human health or the environment.
Table--Draft Risk Assessments Being Made Available for Public Comment
------------------------------------------------------------------------
Chemical review
Registration review case name Docket ID No. manager and contact
and No. information
------------------------------------------------------------------------
Azoxystrobin, 7020............. EPA-HQ-OPP-2009-08 Veronica Dutch,
35. dutch.veronica@epa.gov, (703) 308-
8585.
Bensulfuron-methyl, 7216....... EPA-HQ-OPP-2011-06 Moana Appleyard,
63. appleyard.moana@epa.gov, (703) 308-
8175.
Bifenazate, 7609............... EPA-HQ-OPP-2012-06 Garland Waleko,
33. waleko.garland@epa.gov, (703) 308-
8049.
Boric Acid and Sodium Borate EPA-HQ-OPP-2009-03 Moana Appleyard,
Salts, 0024. 06. appleyard.moana@epa.gov, (703) 308-
8175.
Ethephon, 0382................. EPA-HQ-OPP-2010-00 Marquea D. King,
98. king.marquea@epa.gov, (703) 305-
7432.
Hymexazol, 7016................ EPA-HQ-OPP-2010-01 Caitlin Newcamp,
27. newcamp.caitlin@epa.gov, (703) 347-
0325.
Lithium hypochlorite, 3084..... EPA-HQ-OPP-2013-06 Donna Kamarei,
06. kamarei.donna@epa.gov, (703) 347-
0443.
Pronamide, 0082................ EPA-HQ-OPP-2009-03 Wilhelmena
26. Livingston,
livingston.wilhelmena@epa.gov, (703)
308-8025.
------------------------------------------------------------------------
Azoxystrobin. Draft Human Health and Ecological Risk Assessments
(EPA-HQ-OPP-2009-0835). Azoxystrobin is a systemic fungicide and
antimicrobial registered for use on a variety of terrestrial food and
feed crops, including vegetables, fruits and nuts; terrestrial non-food
crops, including turf and ornamentals; and non-crop sites including
additives for the manufacture of paint, rubber, paper products,
textiles, and adhesives. The Agency has conducted draft human health
and ecological risk assessments for the conventional and antimicrobial
uses of azoxystrobin. A full endangered species assessment has not been
completed for azoxystrobin at this time. For foliar
[[Page 480]]
applications, the ecological risk assessment identifies risks of
concern for aquatic plants, freshwater fish, aquatic invertebrates, and
mammals. For seed treatments, risks of concern are identified for birds
and mammals. The conventional uses of azoxystrobin are associated with
inhalation risks of concern for residential handlers and some
occupational post-application scenarios even with maximum personal
protective equipment (PPE). The antimicrobial uses of azoxystrobin are
not associated with ecological risks of concern, but the human health
risk assessment identifies potential risks of concern for residential
and occupational handlers. Azoxystrobin has not been assessed under the
endocrine disruptor screening program (EDSP) or for risks to
pollinators.
Bensulfuron-methyl. Draft Human Health Risk Assessment (EPA-HQ-OPP-
2011-0663). Bensulfuron-methyl is a sulfonylurea herbicide that acts by
inhibiting acetolactate synthase. Bensulfuron-methyl is registered for
use to control broadleaf weeds and sedges in aquatic rice production.
Tolerances have been established for crayfish, rice, and rice straw.
There are no registered residential uses of bensulfuron-methyl.
Bensulfuron- methyl was first registered in 1989, and a Final Work Plan
was published in February 2012. The ecological risks of bensulfuron-
methyl were assessed together with all other sulfonylureas in the
Preliminary Ecological Risk Assessment for Registration Review of 22
Sulfonylurea Herbicides, published in September 2015. EPA conducted a
human health risk assessment and did not identify any risks of concern
for dietary, residential, occupational, or aggregate exposure.
Bensulfuron-methyl was not on either initial list of chemicals to be
screened under the EDSP, nor has an endangered species or pollinator
assessment been conducted at this time.
Bifenazate. Draft Human Health and Ecological Risk Assessments
(EPA-HQ-OPP-2012-0633). Bifenazate is a selective carbazate miticide/
insecticide that is registered for use to control the motile stage of
mites in agricultural and non-agricultural sites including on bearing
and non-bearing fruit and vegetable crops, cotton, conifer plantations,
ornamentals, and in greenhouses, as well as indoor and outdoor
residential, commercial, institutional, and recreational areas. The
human health non-occupational drift assessment was updated in
registration review for bifenazate and found no risks of concern. In
the recent June 2014, new use assessment, all dietary, residential,
occupational, and aggregate risks were not of concern. In the
ecological assessment, chronic risks of concern were identified for
mammals and birds. There are acute risks identified for listed birds,
freshwater fish, freshwater invertebrates, and estuarine and marine
invertebrates. There is also potential acute and chronic risk to
terrestrial invertebrates. Bifenazate was not on either initial list of
chemicals to be screened under the EDSP, nor has an endangered species
or pollinator assessment been conducted at this time.
Boric Acid and Sodium Borate Salts. Draft Human Health and
Ecological Risk Assessments (EPA-HQ-OPP-2009-0306). Boric acid and its
sodium salts are inorganic compounds with registrations for use as
active ingredients in insecticides, acaricides, herbicides, algaecides,
fungicides, and wood and material preservatives. In small quantities,
boron is an essential nutrient for aquatic vertebrates and
invertebrates and plants. There is also evidence that boron is
essential or, if not essential, beneficial in birds and mammals, in
small quantities. Boric acid and its sodium salts are also present as
inert ingredients in pesticide products and as ingredients in non-
pesticide consumer products. The Agency issued a Final Work Plan for
boric acid in October 2009. The ecological risk assessment identifies
potential risks to terrestrial invertebrates, birds, mammals, reptiles,
terrestrial-phase amphibians, aquatic organisms, and terrestrial
plants. For birds and mammals, risk is primarily associated with the
granular formulations and bait uses. For aquatic organisms, risk is
primarily associated with discharge of swimming pool, hot tub, and spa
effluent directly to surface waters, to storm drains, roadways, and
potentially from storage of treated wood. For terrestrial plants, risk
is primarily associated with discharge of effluent from swimming pools,
hot tubs, and spas. The human health risk assessment did not identify
risks of concern. Boric acid was not on either initial list of
chemicals to be screened under the EDSP, nor has an endangered species
or pollinator assessment been conducted at this time.
Ethephon. Draft Human Health and Ecological Risk Assessments (EPA-
HQ-OPP-2010-0098). Ethephon, 2-chloroethylphosphonic acid, is an
organophosphonate plant growth regulator intended to promote fruit
ripening, abscission, flower induction, breaking of apical dominance
(inhibition of the growth of lateral buds by the terminal bud of a
shoot), and other plant responses through the release of ethylene gas,
a natural plant hormone. EPA conducted a human health risk assessment
and identified aggregate risks of concern for children ages 1-2 years
old. EPA also conducted an ecological risk assessment and identified
potential risks to birds, mammals, and non-target plants. A full
endangered species assessment has not been completed for ethephon at
this time. At this time, ethephon has not been evaluated for its
potential to affect endocrine systems in mammals and wildlife, nor has
an assessment of risks to pollinators been conducted.
Hymexazol. Draft Human Health and Ecological Risk Assessments (EPA-
HQ-OPP-2010-0127). Hymexazol is a systemic fungicide for control of
foliar and soil-borne plant diseases. There is only one existing
registration as a commercial seed treatment for sugar beets. Hymexazol
may be applied only using commercial seed treatment equipment. A Final
Work Plan for hymexazol was published by the Agency in September 2010,
and data were then required in a generic data call-in, dated October
2011. The reviews of the required data have been incorporated into the
draft risk assessments. The Draft Human Health Risk Assessment
identified no dietary risks of concern but identified potential risk to
occupational workers (individuals treating/mixing seed and individuals
doing multiple activities). The Draft Ecological Risk Assessment
identified potential risks to mammals and birds. Hymexazol was not on
either initial list of chemicals to be screened under the EDSP, and a
complete endangered species assessment has not been conducted at this
time.
Lithium hypochlorite. Draft Ecological Risk Assessment (EPA-HQ-OPP-
2013-0606). Lithium hypochlorite is an algicide, disinfectant, and
fungicide. Its primary pesticidal use is to control algae, bacteria,
and mildew in swimming pool water systems, hot tubs, and spas. EPA
conducted a qualitative ecological risk assessment on the swimming pool
uses of lithium hypochlorite as part of registration review. EPA
previously conducted human health and ecological risk assessments at
the time of the Reregistration Eligibility Decision (RED) for lithium
hypochlorite in 1993. Lithium hypochlorite was not on either initial
list of chemicals to be screened under the EDSP, and an endangered
species assessment has not been conducted at this time.
Pronamide. Draft Human Health and Ecological Risk Assessments (EPA-
HQ-OPP-2009-0326). Pronamide, also called propyzamide, 3,5-dichloro-N-
(1,1-dimethyl-2-propynyl)benzamide, is
[[Page 481]]
a selective, systemic, pre-and post-emergence herbicide registered for
the control of grasses and broadleaf weeds in several food and feed
crops as well as woody ornamentals, Christmas trees, grasses grown for
seed or turf (sod), golf course turf, recreational area turf, and
fallow land. EPA conducted a human health risk assessment and did not
identify any risks of concern for dietary, residential, occupational,
or aggregate exposure. EPA also conducted an ecological risk assessment
and identified potential risks to birds, mammals, and plants. An
endangered species and pollinator assessment has not been completed for
pronamide at this time. Pronamide was evaluated for its potential to
affect endocrine systems in mammals and wildlife and the results of the
Agency's review are found in the weight of evidence review in this
registration review docket.
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 the pesticides identified in this
document. 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 may 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
the pesticides identified in this document.
1. Other related information. Additional information on pesticides
identified in this document is available on the Pesticide Registration
Review Status Web page. Information on the Agency's registration review
program and its implementing regulation is available at https://www.epa.gov/pesticide-reevaluation/registration-review-process.
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: December 24, 2015.
Richard P. Keigwin, Jr.,
Director, Pesticide Re-Evaluation Division, Office of Pesticide
Programs.
[FR Doc. 2015-33298 Filed 1-5-16; 8:45 am]
BILLING CODE 6560-50-P