Registration Review Proposed Interim Decisions; Notice of Availability, 47919-47922 [2015-19590]
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Federal Register / Vol. 80, No. 153 / Monday, August 10, 2015 / Notices
Applicants: Tennessee Gas Pipeline
Company, L.L.C.
Description: Section 4(d) Rate Filing:
Clean-Up Filing—2015 to be effective 9/
1/2015.
Filed Date: 8/3/15.
Accession Number: 20150803–5256.
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LLC.
Description: Section 4(d) Rate Filing:
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Filed Date: 8/4/15.
Accession Number: 20150804–5000.
Comments Due: 5 p.m. ET 8/17/15.
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Dated: August 4, 2015.
Nathaniel J. Davis, Sr.,
Deputy Secretary.
[FR Doc. 2015–19563 Filed 8–7–15; 8:45 am]
BILLING CODE 6717–01–P
ENVIRONMENTAL PROTECTION
AGENCY
[EPA–HQ–OPP–2015–0099; FRL–9929–22]
Registration Review Proposed Interim
Decisions; Notice of Availability
Environmental Protection
Agency (EPA).
ACTION: Notice.
AGENCY:
This notice announces the
availability of EPA’s proposed interim
registration review decisions for the
pesticides listed in the table in Unit II
of this notice, and opens a public
comment period on the proposed
decisions. This notice also opens the
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SUMMARY:
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dockets and announces the availability
of EPA’s proposed interim registration
review decisions for 2-propen-1aminium, N,N-dimethyl-N-2-propenyl-,
chloride, homopolymer (or
homopolymer) and tributyltin oxide (or
TBTO); and also opens the docket,
announces the availability of the draft
human health and ecological risk
assessments, and announces the
proposed interim registration review
decision for dipropyl
isocinchomeronate. 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 unreasonable
adverse effects on 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.
DATES: Comments must be received on
or before October 9, 2015.
ADDRESSES: Submit your comments,
identified by the docket identification
(ID) number for the specific pesticide of
interest provided in the table in Unit
II.A., 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
for the pesticide of interest identified in
the table in Unit II.
For general information on the
registration review program, contact:
Richard Dumas, Pesticide Re-Evaluation
Division (7508P), Office of Pesticide
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47919
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 for the
pesticide of interest identified in the
table in Unit II.
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.
II. What action is the Agency taking?
Pursuant to 40 CFR 155.58, this notice
announces the availability of EPA’s
proposed interim registration review
decisions for the pesticides shown in
the following table, and opens a 60-day
public comment period on the proposed
interim decisions.
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Federal Register / Vol. 80, No. 153 / Monday, August 10, 2015 / Notices
TABLE—REGISTRATION REVIEW PROPOSED INTERIM DECISIONS
Docket ID number
Chemical review manager and contact information
Chlorfenapyr 7419 ............................................................
EPA–HQ–OPP–2010–0467
Daminozide 0032 ..............................................................
EPA–HQ–OPP–2009–0242
Dipropyl isocinchomeronate 2215 ....................................
EPA–HQ–OPP–2014–0578
Fenoxaprop p-ethyl 7209 ..................................................
EPA–HQ–OPP–2007–0437
Imazapyr 3078 ..................................................................
Isoxaben 7219 ..................................................................
EPA–HQ–OPP–2014–0200
EPA–HQ–OPP–2007–1038
Paclobutrazol 7002 ...........................................................
2-Propen-1-aminium, N,N-dimethyl-N-2-propenyl-, chloride, homopolymer (or homopolymer) 5024.
Silicon dioxide and silica gel 4081 ...................................
Sulfentrazone 7231 ...........................................................
EPA–HQ–OPP–2006–0109
EPA–HQ–OPP–2015–0255
Tributyltin Oxide (or TBTO) 2620 .....................................
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Registration review case name and number
EPA–HQ–OPP–2014–0801
Margaret Hathaway, hathaway.margaret@epa.gov,
703–305–5076.
Margaret Hathaway, hathaway.margaret@epa.gov,
703–305–5076.
Marianne Mannix, mannix.marianne@epa.gov, 703–
347–0275.
Miguel Zavala, zavala.miguel@epa.gov, 703–347–
0504.
Joel Wolf, wolf.joel@epa.gov, 703–347–0228.
Christina Scheltema, scheltema.christina@epa.gov,
703–308–2201.
Khue Nguyen nguyen.khue@epa.gov 703–347–0248.
Donna Kamarei, kamarei.donna@epa.gov, 703–347–
0443.
James Parker parker.james@epa.gov 703–306–0469.
Christina Scheltema, scheltema.christina@epa.gov,
703–308–2201.
Sandra O’Neill, oneill.sandra@epa.gov, 703–347–0141.
The registration review final decisions
for these cases are dependent on the
assessments of listed species under the
Endangered Species Act (ESA),
determinations on the potential for
endocrine disruption, and/or
assessments of exposure and risk to
pollinators.
Chlorfenapyr (Proposed Interim
Decision). Chlorfenapyr is a member of
the pyrroles class of insecticide/
miticides, which works by disrupting
adenosine triphosphate (ATP)
production, leading to cell dysfunction.
Chlorfenapyr is registered only for
application to fruiting vegetables and
ornamentals in greenhouses; and as a
crack/crevice/spot treatment on indoor
and outdoor residential sites (including
treatment for bed bugs), food/feed
handling areas, indoor and outdoor
commercial sites, and indoor medical
sites. EPA conducted assessments for
both human health and ecological risks.
Possible human health risks of concern
were identified for chlorfenapyr,
including occupational risks and risks
to young children for certain residential
uses. Several risk mitigation measures,
including the termination of the use of
chlorfenapyr on mattresses, are
proposed to address human health risk
concerns. No risks of concern were
identified in the ecological risk
assessment for non-listed species. The
Agency has made a No Effect
determination for chlorfenapyr under
ESA section 7 for all listed species and
a No Habitat Modification
determination for all designated critical
habitats for the currently registered
uses.
Daminozide (Proposed Interim
Decision). Daminozide is a systemic
plant growth regulator registered to
control the development of
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EPA–HQ–OPP–2007–1140
EPA–HQ–OPP–2009–0624
commercially grown container plants. It
is used in nurseries, shadehouses, and
greenhouses, and is applied as a foliar
spray, a use pattern resulting in little or
no potential for off-site drift.
Daminozide has no registered food or
residential uses. EPA conducted
ecological and human health risk
assessments for daminozide, and
concluded that there were no significant
risks of concern. Other than clarifying
application rate information, the Agency
is not calling for changes to daminozide
registrations or labels at this time.
Dipropyl isocinchomeronate
(Combined Docket Opening, Release of
Draft Human Health and Ecological Risk
Assessments, and Proposed Interim
Decision). Dipropyl isocinchomeronate
is registered for use as an insect
repellent for use on humans and
companion animals to repel flies, gnats,
and other flying and biting insects. The
Agency has concluded that there are no
human health risk concerns associated
with the use of dipropyl
isocinchomeronate. Based on the
limited usage, diffusion over a large
treatment area, and the low probability
of non-target organism exposure, the
Agency has not found any ecological
risks of concern associated with
dipropyl isocinchomeronate, and
anticipates making a No Effect
determination for all listed species and
a No Habitat Modification
determination for all designated critical
habitats for listed species. At this time,
the Agency is proposing that no
additional data are needed, and is not
proposing any risk reduction measures
for this case.
Fenoxaprop p-ethyl (Proposed Interim
Decision). FPE is a selective aryloxy
phenoxy-propionate herbicide
registered for use on barley, cotton, rice,
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soybeans, and wheat for post-emergence
control of grassy weeds. Additional nonagricultural use sites include
conservation reserves, ornamentals,
rights-of-way, and turf. EPA’s
Registration Review Proposed Interim
Decision for FPE is: First; no additional
data are required at this time; and
second, certain risk reduction measures
are needed at this time. To address
potential risk to non-target terrestrial
monocots, spray drift management
language is proposed for all FPE product
registrations used on agricultural, wide
area, or rights-of-way use sites. The
Agency also is proposing the
implementation of label language
clarifying use rates, to which the
registrants have already agreed. In
addition, EPA proposes label language
to include recommended herbicideresistance management measures.
Imazapyr (Proposed Interim
Decision). Imazapyr is a non-selective
systemic herbicide registered for use in
pre- and post-emergent treatments to
control terrestrial and aquatic weeds,
including grasses, broadleaf weeds, and
woody species. The registration review
case includes both the acid (imazapyr)
and the isopropylamine salt (imazapyr
IPA). EPA’s Registration Review
Proposed Interim Decision for the case
is that first, no additional data are
required at this time, and second, no
changes to the registrations or their
labeling are needed at this time.
Isoxaben (Proposed Interim Decision).
Isoxaben is a pre-emergent, soil-directed
benzamide herbicide registered for use
in controlling a variety of broad-leaf
weeds. Agricultural uses include grapes
and bearing fruit and nut trees. Nonagricultural uses include turf, lawns,
ornamentals, and landscape mulch.
Quantitative human health and
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ecological risk assessments were
completed for isoxaben. There are no
occupational or residential risks of
concern. There are potential ecological
risks to listed and non-listed aquatic
vascular and terrestrial plants, and risks
to mammals from foliar applications of
isoxaben. The Agency has made the
following Registration Review Proposed
Interim Decision for isoxaben: First, no
additional data are required at this time,
and second, certain risk reduction
measures are needed at this time,
including uniform spray drift
management label language for products
applied by spraying, and recommended
herbicide resistance management
language on all product labels.
Paclobutrazol (Proposed Interim
Decision). Paclobutrazol is a systemic
triazole plant growth regulator
registered for use on nonresidential turf,
on ornamentals in greenhouses and
nurseries, as a tree injection, and as a
seed treatment for certain vegetable
crops. There are no residential uses of
paclobutrazol. EPA conducted risk
assessments for both human health and
ecological risk, and a screening level
endangered species assessment. No
human health risks were identified. The
ecological risk assessment indicated
potential risks to birds, mammals,
terrestrial and aquatic plants, freshwater
and estuarine/marine fish, and
freshwater and estuarine/marine
invertebrates. The Agency is proposing
to modify the application directions for
paclobutrazol to reduce risks to nontarget organisms from runoff. The
screening-level endangered species
assessment did not come to a
conclusion of No Effect to listed species,
therefore, consultation with the Fish
and Wildlife Service and the National
Marine Fisheries Service (‘‘the
Services’’) on the potential risk of
paclobutrazol to listed species will be
necessary.
2-Propen-1-aminium, N,N-dimethylN-2-propenyl-, chloride, homopolymer
(Combined Preliminary Work Plan and
Proposed Interim Decision). There is
one product containing this active
ingredient; it is registered to control
mollusks in potable water supplies. The
Agency did not call-in any data in
support of this registration review case.
Additionally, the Agency did not
conduct a human health or an
environmental risk assessment due to
the lack of exposure concern for the
product’s registered use. Based on the
lack of potential exposure, the Agency
is proposing a No Effect determination
for listed species.
Silicon dioxide and silica gel
(Proposed Interim Decision). Products
containing these two naturally occurring
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active ingredients are registered for use
as insecticides on a variety of
agricultural and residential use sites to
control pests such as ants, cockroaches,
flies, fleas, and ticks. EPA conducted an
ecological risk assessment that included
a screening-level endangered species
assessment. The Agency engaged in
informal consultation with FWS to
reach a ‘‘may affect, but not likely to
adversely affect’’ determination for
direct effects to terrestrial invertebrates
and a No Effect determination for all
other listed taxa. No human health risk
assessment was conducted because no
toxicological endpoints are identified
for the two active ingredients. No risk
mitigation measures for human health
or ecological effects are included in the
silica gel and silicon dioxide Proposed
Interim Decision.
Sulfentrazone (Proposed Interim
Decision). Sulfentrazone is a broad
spectrum, pre-emergence, soil-directed
proto porphyrinogen herbicide used to
control a variety of weeds. It is
registered for use on field crops,
specialty vegetable crops, fruit trees,
ornamentals, and turf grass. EPA
completed quantitative human health
and ecological risk assessments for
sulfentrazone in 2014, and amended the
ecological risk assessment in 2015.
There are no residential risks of
concern; however, there is a risk
concern for pesticide handlers that can
be adequately mitigated by wearing
chemical-resistant gloves. In addition,
there are potential risk concerns for
terrestrial plants. The Agency has made
the following Registration Review
Proposed Interim Decision for
sulfentrazone: First, no additional data
are required at this time; and second,
certain risk reduction measures are
needed at this time. These measures
include uniform spray drift management
language on sulfentrazone labels for
products applied by spraying and
recommended herbicide resistance
management language on all product
labels.
Tributyltin oxide (Combined
Preliminary Work Plan and Proposed
Interim Decision). There are two EPA
registrations for TBTO for rubber
coatings on the sonar domes of nuclear
submarines and for oceanographic
conductivity sensors. Based on the lack
of potential for dietary exposure and no
residential uses, the Agency did not
conduct a human health risk
assessment. Exposure to aquatic
organisms would occur only from the
small amount of TBTO potentially
leaching from sonar domes, and the
Agency believes that risks to non-target,
non-listed species are minimal. TBTO
use as an antifoulant on sonar domes is
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undergoing ESA consultation with the
Department of Defense, EPA, and the
Services for compounds covered under
EPA’s Uniform National Discharge
Standards. At this time, the Agency is
proposing that no additional data are
needed, and is not proposing any risk
reduction measures for this case.
The registration review docket for a
pesticide includes earlier documents
related to the registration review of the
case. For example, the review typically
opens with the availability of a
Summary Document, containing a
Preliminary Work Plan, for public
comment. A Final Work Plan typically
is placed in the docket following public
comment on the initial docket.
Following a period for public comment
on the proposed interim decisions
announced in this notice, the Agency
will issue interim registration review
decisions for products containing the
affected active ingredients.
The registration review program is
being conducted under congressionally
mandated time frames, and EPA
recognizes the need both to make timely
decisions and to involve the public.
Section 3(g) of the Federal Insecticide,
Fungicide, and Rodenticide Act (FIFRA)
(7 U.S.C. 136a(g)) required EPA to
establish by regulation procedures for
reviewing pesticide registrations,
originally with a goal of reviewing each
pesticide’s registration every 15 years to
ensure that a pesticide continues to
meet the FIFRA standard for
registration. The Agency’s final rule to
implement this program was issued in
the Federal Register of August 9, 2006
(71 FR 45720) (FRL–8080–4) and
became effective in October 2006, and
appears at 40 CFR part 155, subpart C.
The Pesticide Registration Improvement
Act of 2003 (PRIA) was amended and
extended in September 2007. FIFRA, as
amended by PRIA in 2007, requires EPA
to complete registration review
decisions by October 1, 2022, for all
pesticides registered as of October 1,
2007.
The registration review final rule at 40
CFR 155.58(a) provides for a minimum
60-day public comment period on all
proposed interim registration review
decisions. This comment period is
intended to provide an opportunity for
public input and a mechanism for
initiating any necessary amendments to
the proposed interim decisions. All
comments should be submitted using
the methods in ADDRESSES, and must be
received by EPA on or before the closing
date. These comments will become part
of the docket for the pesticides included
in the table in Unit II. Comments
received after the close of the comment
period will be marked ‘‘late.’’ EPA is not
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required to consider these late
comments.
The Agency will carefully consider all
comments received by the closing date
and, as appropriate, will provide a
‘‘Response to Comments Memorandum’’
in the docket for each of the pesticides
included in the table in Unit II. The
interim registration review decision will
explain the effect that any such
comments had on the decision and
provide the Agency’s response to
significant comments, as needed.
Background on the registration review
program is provided at: https://
www2.epa.gov/pesticide-reevaluation.
Links to earlier documents related to the
registration review of the pesticide cases
identified in this notice are provided on
the Pesticide Chemical Search data base
accessible at: https://iaspub.epa.gov/
apex/pesticides/f?p=chemicalsearch.
Authority: 7 U.S.C. 136 et seq.
Dated: July 30, 2015.
Richard P. Keigwin, Jr.,
Director, Pesticide Re-Evaluation Division,
Office of Pesticide Programs.
[FR Doc. 2015–19590 Filed 8–7–15; 8:45 am]
BILLING CODE 6560–50–P
ENVIRONMENTAL PROTECTION
AGENCY
[FRL–9932–09-Region 2]
Proposed Settlement Pursuant Section
122(h) of CERCLA Relating to the
Gowanus Canal Superfund Site,
Brooklyn, Kings County, New York
Environmental Protection
Agency (EPA).
ACTION: Notice; request for public
comment.
AGENCY:
In accordance with Section
122(i) of the Comprehensive
Environmental Response,
Compensation, and Liability Act of
1980, as amended (‘‘CERCLA’’), 42
U.S.C. 9622(i), notice is hereby given by
the U.S. Environmental Protection
Agency (‘‘EPA’’), Region 2, of a
proposed settlement agreement
pursuant to Section 122(h) of CERCLA,
entered into by and EPA, Region 2, and
Patterson Fuel Oil Co., Inc. (‘‘Settling
Party’’), pertaining to the Gowanus
Canal Superfund Site (‘‘Site’’) located in
Brooklyn, Kings County, New York.
Under the Settlement Agreement, the
Settling Party agrees to pay EPA
$100,000.00 for the recovery of response
actions incurred at the Site.
The Settlement Agreement includes a
covenant by EPA not to sue or to take
administrative action against the
Settling Party pursuant to Sections 106
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SUMMARY:
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and 107(a) of CERCLA, 42 U.S.C. 9606
and 9607(a), with regard to the Site, as
defined in the Settlement Agreement.
For thirty (30) days following the date
of publication of this notice, EPA will
receive written comments relating to the
Settlement Agreement. EPA will
consider all comments received and
may modify or withdraw its consent to
the Settlement Agreement if comments
received disclose facts or considerations
that indicate that the proposed
Settlement Agreement is inappropriate,
improper or inadequate. EPA’s response
to any comments received will be
available for public inspection at EPA
Region 2 offices, 290 Broadway, New
York, New York 10007–1866.
DATES: Comments must be submitted on
or before September 9, 2015.
ADDRESSES: The proposed Settlement
Agreement can be viewed at https://
www.epa.gov/region02/superfund/npl/
gowanus/additionaldocs.html. It is also
available for public inspection at EPA
Region 2 offices at 290 Broadway, New
York, New York 10007–1866.
A copy may also be obtained from
Brian Carr, Assistant Regional Counsel,
New York/Caribbean Superfund Branch,
Office of Regional Counsel, U.S. EPA
Region 2, 290 Broadway, 17th Floor,
New York, New York 10007–1866, 212–
637–3170, carr.brian@epa.gov.
Comments should reference the
Gowanus Canal Superfund Site,
Brooklyn, New York. Index No.
CERCLA–02–2015–2008 and should be
sent by mail or email to Brian Carr,
Assistant Regional Counsel, at the
address or email address above.
FOR FURTHER INFORMATION CONTACT:
Brian Carr, Assistant Regional Counsel,
at the address, email or telephone
number stated above.
Dated: July 27, 2015.
Walter Mugdan,
Director, Emergency and Remedial Response
Division, U.S. Environmental Protection
Agency, Region 2.
[FR Doc. 2015–19601 Filed 8–7–15; 8:45 am]
BILLING CODE 6560–50–P
ENVIRONMENTAL PROTECTION
AGENCY
[EPA–HQ–ORD–2015–0467; FRL–9932–08–
ORD]
Board of Scientific Counselors (BOSC)
Safe and Sustainable Water Resources
Subcommittee Meeting—August 2015;
Public Requests Correction
Environmental Protection
Agency (EPA).
ACTION: Notice; correction.
AGENCY:
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On July 30, 2015, the U.S.
Environmental Protection Agency
(EPA), Office of Research and
Development (ORD), gave notice of a
meeting of the Board of Scientific
Counselors (BOSC) Safe and Sustainable
Water Resources Subcommittee in the
Federal Register. On Page 45536,
Column 3, in the DATES section, EPA
inadvertently listed the date by which
members of the public should request a
draft agenda or request an opportunity
to make oral presentations at the
meeting as July 25, 2015. The correct
date by which requests should be made
is August 25, 2015.
FOR FURTHER INFORMATION CONTACT: The
Designated Federal Officer via mail at:
Cindy Roberts, Mail Code 8104R, Office
of Science Policy, Office of Research
and Development, U.S. Environmental
Protection Agency, 1200 Pennsylvania
Ave. NW., Washington, DC 20460; via
phone/voice mail at: (202) 564–1999; or
via email at: roberts.cindy@epa.gov.
SUMMARY:
Dated: July 31, 2015.
Fred S. Hauchman,
Director, Office of Science Policy.
[FR Doc. 2015–19592 Filed 8–7–15; 8:45 am]
BILLING CODE 6560–50–P
ENVIRONMENTAL PROTECTION
AGENCY
Proposed Partial Consent Decree,
Clean Air Act Citizen Suit
Environmental Protection
Agency (EPA).
ACTION: Notice of proposed partial
consent decree; request for public
comment.
AGENCY:
In accordance with section
113(g) of the Clean Air Act, as amended
(‘‘CAA’’ or the ‘‘Act’’), notice is hereby
given of a proposed partial consent
decree to address a lawsuit filed by the
Sierra Club in the United States District
Court for the District of Columbia:
Sierra Club v. EPA, Civil Action No. 10–
cv–1541 (CKK) (D.D.C.) (filed Sept. 14,
2010). Plaintiff filed a lawsuit alleging
that Gina McCarthy, in her official
capacity as Administrator of the United
States Environmental Protection Agency
(‘‘EPA’’), failed to perform duties
mandated by the CAA to: (1) Promulgate
a federal implementation plan (‘‘FIP’’)
for the State of Texas for the 1997 fine
particulate matter (‘‘PM2.5’’) and ozone
national ambient air quality standards
(‘‘NAAQS’’); (2) promulgate a FIP for the
State of Texas for the 1997 ozone
NAAQS; and (3) take final approval/
disapproval action on the state
implementation plan (‘‘SIP’’) that Texas
submitted for implementation of the
SUMMARY:
E:\FR\FM\10AUN1.SGM
10AUN1
Agencies
[Federal Register Volume 80, Number 153 (Monday, August 10, 2015)]
[Notices]
[Pages 47919-47922]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2015-19590]
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ENVIRONMENTAL PROTECTION AGENCY
[EPA-HQ-OPP-2015-0099; FRL-9929-22]
Registration Review Proposed Interim Decisions; Notice of
Availability
AGENCY: Environmental Protection Agency (EPA).
ACTION: Notice.
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SUMMARY: This notice announces the availability of EPA's proposed
interim registration review decisions for the pesticides listed in the
table in Unit II of this notice, and opens a public comment period on
the proposed decisions. This notice also opens the dockets and
announces the availability of EPA's proposed interim registration
review decisions for 2-propen-1-aminium, N,N-dimethyl-N-2-propenyl-,
chloride, homopolymer (or homopolymer) and tributyltin oxide (or TBTO);
and also opens the docket, announces the availability of the draft
human health and ecological risk assessments, and announces the
proposed interim registration review decision for dipropyl
isocinchomeronate. 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 unreasonable
adverse effects on 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.
DATES: Comments must be received on or before October 9, 2015.
ADDRESSES: Submit your comments, identified by the docket
identification (ID) number for the specific pesticide of interest
provided in the table in Unit II.A., 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 for the pesticide of interest identified in the table in Unit
II.
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.
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 for the pesticide of interest
identified in the table in Unit II.
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.
II. What action is the Agency taking?
Pursuant to 40 CFR 155.58, this notice announces the availability
of EPA's proposed interim registration review decisions for the
pesticides shown in the following table, and opens a 60-day public
comment period on the proposed interim decisions.
[[Page 47920]]
Table--Registration Review Proposed Interim Decisions
----------------------------------------------------------------------------------------------------------------
Registration review case name and Chemical review manager and
number Docket ID number contact information
----------------------------------------------------------------------------------------------------------------
Chlorfenapyr 7419.................... EPA-HQ-OPP-2010-0467 Margaret Hathaway,
hathaway.margaret@epa.gov,
703-305-5076.
Daminozide 0032...................... EPA-HQ-OPP-2009-0242 Margaret Hathaway,
hathaway.margaret@epa.gov,
703-305-5076.
Dipropyl isocinchomeronate 2215...... EPA-HQ-OPP-2014-0578 Marianne Mannix,
mannix.marianne@epa.gov, 703-
347-0275.
Fenoxaprop p-ethyl 7209.............. EPA-HQ-OPP-2007-0437 Miguel Zavala,
zavala.miguel@epa.gov, 703-
347-0504.
Imazapyr 3078........................ EPA-HQ-OPP-2014-0200 Joel Wolf, wolf.joel@epa.gov,
703-347-0228.
Isoxaben 7219........................ EPA-HQ-OPP-2007-1038 Christina Scheltema,
scheltema.christina@epa.gov,
703-308-2201.
Paclobutrazol 7002................... EPA-HQ-OPP-2006-0109 Khue Nguyen
nguyen.khue@epa.gov 703-347-
0248.
2-Propen-1-aminium, N,N-dimethyl-N-2- EPA-HQ-OPP-2015-0255 Donna Kamarei,
propenyl-, chloride, homopolymer (or kamarei.donna@epa.gov, 703-
homopolymer) 5024. 347-0443.
Silicon dioxide and silica gel 4081.. EPA-HQ-OPP-2007-1140 James Parker
parker.james@epa.gov 703-306-
0469.
Sulfentrazone 7231................... EPA-HQ-OPP-2009-0624 Christina Scheltema,
scheltema.christina@epa.gov,
703-308-2201.
Tributyltin Oxide (or TBTO) 2620..... EPA-HQ-OPP-2014-0801 Sandra O'Neill,
oneill.sandra@epa.gov, 703-
347-0141.
----------------------------------------------------------------------------------------------------------------
The registration review final decisions for these cases are
dependent on the assessments of listed species under the Endangered
Species Act (ESA), determinations on the potential for endocrine
disruption, and/or assessments of exposure and risk to pollinators.
Chlorfenapyr (Proposed Interim Decision). Chlorfenapyr is a member
of the pyrroles class of insecticide/miticides, which works by
disrupting adenosine triphosphate (ATP) production, leading to cell
dysfunction. Chlorfenapyr is registered only for application to
fruiting vegetables and ornamentals in greenhouses; and as a crack/
crevice/spot treatment on indoor and outdoor residential sites
(including treatment for bed bugs), food/feed handling areas, indoor
and outdoor commercial sites, and indoor medical sites. EPA conducted
assessments for both human health and ecological risks. Possible human
health risks of concern were identified for chlorfenapyr, including
occupational risks and risks to young children for certain residential
uses. Several risk mitigation measures, including the termination of
the use of chlorfenapyr on mattresses, are proposed to address human
health risk concerns. No risks of concern were identified in the
ecological risk assessment for non-listed species. The Agency has made
a No Effect determination for chlorfenapyr under ESA section 7 for all
listed species and a No Habitat Modification determination for all
designated critical habitats for the currently registered uses.
Daminozide (Proposed Interim Decision). Daminozide is a systemic
plant growth regulator registered to control the development of
commercially grown container plants. It is used in nurseries,
shadehouses, and greenhouses, and is applied as a foliar spray, a use
pattern resulting in little or no potential for off-site drift.
Daminozide has no registered food or residential uses. EPA conducted
ecological and human health risk assessments for daminozide, and
concluded that there were no significant risks of concern. Other than
clarifying application rate information, the Agency is not calling for
changes to daminozide registrations or labels at this time.
Dipropyl isocinchomeronate (Combined Docket Opening, Release of
Draft Human Health and Ecological Risk Assessments, and Proposed
Interim Decision). Dipropyl isocinchomeronate is registered for use as
an insect repellent for use on humans and companion animals to repel
flies, gnats, and other flying and biting insects. The Agency has
concluded that there are no human health risk concerns associated with
the use of dipropyl isocinchomeronate. Based on the limited usage,
diffusion over a large treatment area, and the low probability of non-
target organism exposure, the Agency has not found any ecological risks
of concern associated with dipropyl isocinchomeronate, and anticipates
making a No Effect determination for all listed species and a No
Habitat Modification determination for all designated critical habitats
for listed species. At this time, the Agency is proposing that no
additional data are needed, and is not proposing any risk reduction
measures for this case.
Fenoxaprop p-ethyl (Proposed Interim Decision). FPE is a selective
aryloxy phenoxy-propionate herbicide registered for use on barley,
cotton, rice, soybeans, and wheat for post-emergence control of grassy
weeds. Additional non-agricultural use sites include conservation
reserves, ornamentals, rights-of-way, and turf. EPA's Registration
Review Proposed Interim Decision for FPE is: First; no additional data
are required at this time; and second, certain risk reduction measures
are needed at this time. To address potential risk to non-target
terrestrial monocots, spray drift management language is proposed for
all FPE product registrations used on agricultural, wide area, or
rights-of-way use sites. The Agency also is proposing the
implementation of label language clarifying use rates, to which the
registrants have already agreed. In addition, EPA proposes label
language to include recommended herbicide-resistance management
measures.
Imazapyr (Proposed Interim Decision). Imazapyr is a non-selective
systemic herbicide registered for use in pre- and post-emergent
treatments to control terrestrial and aquatic weeds, including grasses,
broadleaf weeds, and woody species. The registration review case
includes both the acid (imazapyr) and the isopropylamine salt (imazapyr
IPA). EPA's Registration Review Proposed Interim Decision for the case
is that first, no additional data are required at this time, and
second, no changes to the registrations or their labeling are needed at
this time.
Isoxaben (Proposed Interim Decision). Isoxaben is a pre-emergent,
soil-directed benzamide herbicide registered for use in controlling a
variety of broad-leaf weeds. Agricultural uses include grapes and
bearing fruit and nut trees. Non-agricultural uses include turf, lawns,
ornamentals, and landscape mulch. Quantitative human health and
[[Page 47921]]
ecological risk assessments were completed for isoxaben. There are no
occupational or residential risks of concern. There are potential
ecological risks to listed and non-listed aquatic vascular and
terrestrial plants, and risks to mammals from foliar applications of
isoxaben. The Agency has made the following Registration Review
Proposed Interim Decision for isoxaben: First, no additional data are
required at this time, and second, certain risk reduction measures are
needed at this time, including uniform spray drift management label
language for products applied by spraying, and recommended herbicide
resistance management language on all product labels.
Paclobutrazol (Proposed Interim Decision). Paclobutrazol is a
systemic triazole plant growth regulator registered for use on
nonresidential turf, on ornamentals in greenhouses and nurseries, as a
tree injection, and as a seed treatment for certain vegetable crops.
There are no residential uses of paclobutrazol. EPA conducted risk
assessments for both human health and ecological risk, and a screening
level endangered species assessment. No human health risks were
identified. The ecological risk assessment indicated potential risks to
birds, mammals, terrestrial and aquatic plants, freshwater and
estuarine/marine fish, and freshwater and estuarine/marine
invertebrates. The Agency is proposing to modify the application
directions for paclobutrazol to reduce risks to non-target organisms
from runoff. The screening-level endangered species assessment did not
come to a conclusion of No Effect to listed species, therefore,
consultation with the Fish and Wildlife Service and the National Marine
Fisheries Service (``the Services'') on the potential risk of
paclobutrazol to listed species will be necessary.
2-Propen-1-aminium, N,N-dimethyl-N-2-propenyl-, chloride,
homopolymer (Combined Preliminary Work Plan and Proposed Interim
Decision). There is one product containing this active ingredient; it
is registered to control mollusks in potable water supplies. The Agency
did not call-in any data in support of this registration review case.
Additionally, the Agency did not conduct a human health or an
environmental risk assessment due to the lack of exposure concern for
the product's registered use. Based on the lack of potential exposure,
the Agency is proposing a No Effect determination for listed species.
Silicon dioxide and silica gel (Proposed Interim Decision).
Products containing these two naturally occurring active ingredients
are registered for use as insecticides on a variety of agricultural and
residential use sites to control pests such as ants, cockroaches,
flies, fleas, and ticks. EPA conducted an ecological risk assessment
that included a screening-level endangered species assessment. The
Agency engaged in informal consultation with FWS to reach a ``may
affect, but not likely to adversely affect'' determination for direct
effects to terrestrial invertebrates and a No Effect determination for
all other listed taxa. No human health risk assessment was conducted
because no toxicological endpoints are identified for the two active
ingredients. No risk mitigation measures for human health or ecological
effects are included in the silica gel and silicon dioxide Proposed
Interim Decision.
Sulfentrazone (Proposed Interim Decision). Sulfentrazone is a broad
spectrum, pre-emergence, soil-directed proto porphyrinogen herbicide
used to control a variety of weeds. It is registered for use on field
crops, specialty vegetable crops, fruit trees, ornamentals, and turf
grass. EPA completed quantitative human health and ecological risk
assessments for sulfentrazone in 2014, and amended the ecological risk
assessment in 2015. There are no residential risks of concern; however,
there is a risk concern for pesticide handlers that can be adequately
mitigated by wearing chemical-resistant gloves. In addition, there are
potential risk concerns for terrestrial plants. The Agency has made the
following Registration Review Proposed Interim Decision for
sulfentrazone: First, no additional data are required at this time; and
second, certain risk reduction measures are needed at this time. These
measures include uniform spray drift management language on
sulfentrazone labels for products applied by spraying and recommended
herbicide resistance management language on all product labels.
Tributyltin oxide (Combined Preliminary Work Plan and Proposed
Interim Decision). There are two EPA registrations for TBTO for rubber
coatings on the sonar domes of nuclear submarines and for oceanographic
conductivity sensors. Based on the lack of potential for dietary
exposure and no residential uses, the Agency did not conduct a human
health risk assessment. Exposure to aquatic organisms would occur only
from the small amount of TBTO potentially leaching from sonar domes,
and the Agency believes that risks to non-target, non-listed species
are minimal. TBTO use as an antifoulant on sonar domes is undergoing
ESA consultation with the Department of Defense, EPA, and the Services
for compounds covered under EPA's Uniform National Discharge Standards.
At this time, the Agency is proposing that no additional data are
needed, and is not proposing any risk reduction measures for this case.
The registration review docket for a pesticide includes earlier
documents related to the registration review of the case. For example,
the review typically opens with the availability of a Summary Document,
containing a Preliminary Work Plan, for public comment. A Final Work
Plan typically is placed in the docket following public comment on the
initial docket. Following a period for public comment on the proposed
interim decisions announced in this notice, the Agency will issue
interim registration review decisions for products containing the
affected active ingredients.
The registration review program is being conducted under
congressionally mandated time frames, and EPA recognizes the need both
to make timely decisions and to involve the public. Section 3(g) of the
Federal Insecticide, Fungicide, and Rodenticide Act (FIFRA) (7 U.S.C.
136a(g)) required EPA to establish by regulation procedures for
reviewing pesticide registrations, originally with a goal of reviewing
each pesticide's registration every 15 years to ensure that a pesticide
continues to meet the FIFRA standard for registration. The Agency's
final rule to implement this program was issued in the Federal Register
of August 9, 2006 (71 FR 45720) (FRL-8080-4) and became effective in
October 2006, and appears at 40 CFR part 155, subpart C. The Pesticide
Registration Improvement Act of 2003 (PRIA) was amended and extended in
September 2007. FIFRA, as amended by PRIA in 2007, requires EPA to
complete registration review decisions by October 1, 2022, for all
pesticides registered as of October 1, 2007.
The registration review final rule at 40 CFR 155.58(a) provides for
a minimum 60-day public comment period on all proposed interim
registration review decisions. This comment period is intended to
provide an opportunity for public input and a mechanism for initiating
any necessary amendments to the proposed interim decisions. All
comments should be submitted using the methods in ADDRESSES, and must
be received by EPA on or before the closing date. These comments will
become part of the docket for the pesticides included in the table in
Unit II. Comments received after the close of the comment period will
be marked ``late.'' EPA is not
[[Page 47922]]
required to consider these late comments.
The Agency will carefully consider all comments received by the
closing date and, as appropriate, will provide a ``Response to Comments
Memorandum'' in the docket for each of the pesticides included in the
table in Unit II. The interim registration review decision will explain
the effect that any such comments had on the decision and provide the
Agency's response to significant comments, as needed.
Background on the registration review program is provided at:
https://www2.epa.gov/pesticide-reevaluation. Links to earlier documents
related to the registration review of the pesticide cases identified in
this notice are provided on the Pesticide Chemical Search data base
accessible at: https://iaspub.epa.gov/apex/pesticides/f?p=chemicalsearch.
Authority: 7 U.S.C. 136 et seq.
Dated: July 30, 2015.
Richard P. Keigwin, Jr.,
Director, Pesticide Re-Evaluation Division, Office of Pesticide
Programs.
[FR Doc. 2015-19590 Filed 8-7-15; 8:45 am]
BILLING CODE 6560-50-P