Registration Review Proposed Interim Decisions; Notice of Availability, 15785-15787 [2015-06860]
Download as PDF
Federal Register / Vol. 80, No. 57 / Wednesday, March 25, 2015 / Notices
You may also register online at
https://www.ferc.gov/docs-filing/
esubscription.asp to be notified via
email of new filings and issuances
related to this or other pending projects.
For assistance, contact FERC Online
Support.
n. Scoping Process
The Commission intends to prepare
an environmental assessment (EA) on
the project in accordance with the
National Environmental Policy Act. The
EA will consider both site-specific and
cumulative environmental impacts and
reasonable alternatives to the proposed
action.
Scoping Meetings
FERC staff will conduct one agency
scoping meeting and one public
meeting. The agency scoping meeting
will focus on resource agency and nongovernmental organization (NGO)
concerns, while the public scoping
meeting is primarily for public input.
All interested individuals,
organizations, and agencies are invited
to attend one or both of the meetings,
and to assist the staff in identifying the
scope of the environmental issues that
should be analyzed in the EA. The times
and locations of these meetings are as
follows:
Agency Scoping Meeting
DATE: Tuesday, April 21, 2015.
TIME: 1 p.m. (EDT).
PLACE: Watauga County Center.
ADDRESS: 971 W. King Street, Boone,
NC 28607.
Public Scoping Meeting
DATE: Tuesday, April 21, 2015.
TIME: 7 p.m. (EDT).
PLACE: Watauga County Center.
ADDRESS: 971 W. King Street, Boone,
NC 28607.
Copies of the Scoping Document
(SD1) outlining the subject areas to be
addressed in the EA were distributed to
the parties on the Commission’s mailing
list. Copies of the SD1 will be available
at the scoping meeting or may be
viewed on the web at https://
www.ferc.gov using the ‘‘eLibrary’’ link
(see item m above).
rljohnson on DSK3VPTVN1PROD with NOTICES
Environmental Site Review
The Applicant and FERC staff will
conduct a project Environmental Site
Review. The time and location of this
meeting is as follows:
PROJECT: Ward Mill Hydroelectric
Project.
DATE: Tuesday, April 21, 2015.
TIME: 3:30 p.m. (EDT).
LOCATION: Watauga County Center
Parking Lot, 971 W. King Street, Boone,
NC 28607.
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15:26 Mar 24, 2015
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All interested individuals,
organizations, and agencies are invited
to attend. All participants should meet
at the time and location specified above.
All participants are responsible for their
own transportation to the site. Anyone
with questions about the Environmental
Site Review should contact Andrew C.
Givens, Cardinal Energy Service, Inc.,
620 N. West St., Suite 103, Raleigh,
North Carolina 27603, (919) 834–0909
on or before April 14, 2015.
Objectives
At the scoping meetings, the staff will:
(1) Summarize the environmental issues
tentatively identified for analysis in the
EA; (2) solicit from the meeting
participants all available information,
especially quantifiable data, on the
resources at issue; (3) encourage
statements from experts and the public
on issues that should be analyzed in the
EA, including viewpoints in opposition
to, or in support of, the staff’s
preliminary views; (4) determine the
resource issues to be addressed in the
EA; and (5) identify those issues that
require a detailed analysis, as well as
those issues that do not require a
detailed analysis.
Procedures
The meetings are recorded by a
stenographer and become part of the
formal record of the Commission
proceeding on the project.
Individuals, organizations, and
agencies with environmental expertise
and concerns are encouraged to attend
the meeting and to assist the staff in
defining and clarifying the issues to be
addressed in the EA.
Dated: March 18, 2015.
Kimberly D. Bose,
Secretary.
[FR Doc. 2015–06742 Filed 3–24–15; 8:45 am]
BILLING CODE 6717–01–P
ENVIRONMENTAL PROTECTION
AGENCY
[EPA–HQ–OPP–2015–0059; FRL–9923–76]
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 on certain
pesticides and opens a public comment
period on the proposed interim
decisions. Registration review is EPA’s
periodic review of pesticide
SUMMARY:
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15785
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.March 25, 2015
DATES: Comments must be received on
or before May 26, 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.,
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.
E:\FR\FM\25MRN1.SGM
25MRN1
15786
Federal Register / Vol. 80, No. 57 / Wednesday, March 25, 2015 / Notices
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.
TABLE—REGISTRATION REVIEW PROPOSED INTERIM DECISIONS
Pesticide Docket ID No.
Debacarb (2–EEEBC) (Case 4031)
Maleic Hydrazide (Case 0381) .......
Soap Salts (Case 4083) ..................
rljohnson on DSK3VPTVN1PROD with NOTICES
Registration review case name and
No.
EPA–HQ–OPP–2008–0802 ...........
EPA–HQ–OPP–2009–0387 ...........
EPA–HQ–OPP–2008–0519 ...........
Debacarb (2–EEEBC) (Proposed
Interim Decision). Debacarb is a
fungicide registered for use to control
certain diseases in ornamental trees.
The fungicide is applied to mature trees
by injection through the trunk. EPA has
completed a draft ecological risk
assessment, including a screening-level
listed species assessment. A human
health risk assessment is not needed
because the method of application
limits the possibility for applicator or
other human exposure. Direct adverse
effects are not expected for birds,
reptiles, terrestrial-phase amphibians,
mammals, and terrestrial plants. The
Agency has made a No Effects (NE)
determination for all federally-listed
species within these groups and a No
Habitat Modification determination for
all designated critical habitats
associated with these species for the
currently registered uses of debacarb.
Risks currently cannot be precluded for
aquatic receptors and terrestrial
invertebrates. At this time, to eliminate
uncertainty and reduce potential risks to
non-listed aquatic species, the Agency is
proposing restrictions on application to
trees near waterbodies. To reduce
uncertainty and potential risks to insect
pollinators, the Agency is proposing
that applications to trees be limited to
the post-bloom period. This proposed
interim decision does not cover the
Endocrine Disruptor Screening program
(EDSP) component of this registration
review case, nor does it provide a
complete Endangered Species
assessment (ESA) for debacarb.
However, pending the outcome of this
action, the EPA is planning to issue an
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15:26 Mar 24, 2015
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Chemical review manager, telephone No., email address
Roy Johnson, 703–347–0492, johnson.roy@epa.gov.
Ricardo Jones, 703–347–0493, jones.ricardo@epa.gov.
Eric Miederhoff, 703–347–8028 miederhoff.eric@epa.gov.
interim registration review decision for
debacarb.
Maleic Hydrazide (Proposed Interim
Decision). The registration review
docket for maleic hydrazide (EPA–HQ–
OPP–2009–0387) opened in September
2009. Maleic hydrazide is a systemic
plant growth regulator registered for use
on tobacco, potato, onions, non-bearing
citrus, turf, utility and highway rightsof-way, airports, industrial land, lawns,
recreational areas, ornamental/shade
trees and ornamental plants. Uses
include residential use on turf and
lawns as a perimeter or spot treatment.
EPA published draft human health and
ecological risk assessments in July 2014.
No human health risks of concern were
identified. The Agency also completed
an ecological risk assessment. The
results of this quantitative risk
assessment indicates that the currently
labeled rates of maleic hydrazide pose a
potential for risk to non-target terrestrial
birds and terrestrial invertebrates. In
addition, applications may impact
sensitive species of semi-aquatic and
terrestrial monocotyledonous plants
(monocots). The Agency completed a
screening-level ESA and made a ‘‘no
effects’’ determination for the following
taxa: Aquatic plants and aquatic
freshwater and estuarine/marine
organisms. For all other species
applications ‘‘may affect’’ or are
uncertain. Maleic hydrazide has not
been evaluated under the EDSP nor has
it completed ESA section 7 consultation
with the U.S. Fish and Wildlife Service
and the National Marine and Fisheries
Service (Services). Therefore, the
Agency’s final registration review
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decision is dependent upon the result of
the evaluation of potential endocrine
disruptor risk and consultation with the
Services for endangered species.
Pending the outcome of this action, the
EPA is planning to issue an interim
registration review decision for maleic
hydrazide.
Soap Salts (Proposed Interim
Decision). The registration review
docket for soap salts (EPA–HQ–OPP–
2008–0519) opened in September 2008.
Soap Salts are used as acaricides,
herbicides, and insecticides on food and
non-food crops in various settings,
chiefly residential and agricultural.
Ammonium and sodium soap salts are
also used as animal repellants. EPA
published draft human health and
ecological risk assessments in March
2013. EPA conducted a human health
risk assessment and did not identify any
risks of concern. No human health
mitigation is being proposed by the
Agency for the soap salts at this time.
The Agency also conducted an
ecological risk assessment for the
current uses of the soap salts. The
screening-level risk assessment did find
the potential for minor risk to terrestrial
plants and aquatic organisms from the
use of potassium and ammonium salts.
However, the Agency believes there is
little actual risk to non-target plants
exposed to soap salts due to the rapid
degradation of soap salts in surface
water runoff, which was not accounted
for in the risk assessment model, and
the inherent insolubility and low
toxicity of the soap salts. Therefore, the
Agency has no risk concerns from the
terrestrial or aquatic assessments and is
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rljohnson on DSK3VPTVN1PROD with NOTICES
Federal Register / Vol. 80, No. 57 / Wednesday, March 25, 2015 / Notices
not proposing ecological risk mitigation
at this time. The Agency also completed
a screening-level endangered and
threatened (listed) species assessment
for soap salts and identified potential
risks to several taxa: Freshwater
invertebrates, estuarine/marine
invertebrates, and terrestrial plants.
However, at this time in registration
review, it is premature to make an
endangered species effects
determination for federally listed
species and their designated critical
habitats under ESA. Also, the soap salts
have not yet been evaluated under the
EDSP. Therefore, the Agency’s final
registration review decision is
dependent upon the results of the
evaluation of risks to threatened and
endangered species and of potential
endocrine disruptor risk. Pending the
outcome of this action, the EPA is
planning to issue an interim registration
review decision for the soap salts.
The registration review docket for a
pesticide includes earlier documents
related to the registration review of the
case. For example, the review opened
with a Summary Document, containing
a Preliminary Work Plan, for public
comment. A Final Work Plan was
placed in the docket following public
comment on the initial docket. The
documents in the docket describe EPA’s
rationales for conducting additional risk
assessments, as well as the Agency’s
subsequent risk findings and
consideration of possible risk mitigation
measures. A proposed interim
registration review decision is
supported by the rationales included in
those documents. Following public
comment on a proposed decision, the
Agency will issue interim registration
review decisions for products
containing the pesticides listed in the
table in Unit II.
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
August 2006 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
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15:26 Mar 24, 2015
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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 decision. 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
required to consider these late
comments.
The Agency will carefully consider all
comments received by the closing date
and will provide a ‘‘Response to
Comments Memorandum’’ in the docket
as appropriate. The final registration
review decision will explain the effect
that any comments had on the decision.
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 these pesticides
are provided at: https://www.epa.gov/
oppsrrd1/registration_review/reg_
review_status.htm.
Authority: 7 U.S.C. 136 et seq.
Dated: March 17, 2015.
Richard P. Keigwin, Jr.,
Director, Pesticide Re-Evaluation Division,
Office of Pesticide Programs.
[FR Doc. 2015–06860 Filed 3–24–15; 8:45 am]
BILLING CODE 6560–50–P
ENVIRONMENTAL PROTECTION
AGENCY
[EPA–HQ–OPPT–2013–0677; FRL–9924–68]
Receipt of Test Data Under the Toxic
Substances Control Act
Environmental Protection
Agency (EPA).
ACTION: Notice.
AGENCY:
EPA is announcing its receipt
of test data submitted pursuant to a test
rule issued by EPA under the Toxic
Substances Control Act (TSCA). As
required by TSCA, this document
identifies each chemical substance and/
or mixture for which test data have been
received; the uses or intended uses of
such chemical substance and/or
mixture; and describes the nature of the
SUMMARY:
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15787
test data received. Each chemical
substance and/or mixture related to this
announcement is identified in Unit I.
under SUPPLEMENTARY INFORMATION.
FOR FURTHER INFORMATION CONTACT:
For technical information contact:
Kathy Calvo, Chemical Control Division
(7405M), Office of Pollution Prevention
and Toxics, Environmental Protection
Agency, 1200 Pennsylvania Ave. NW.,
Washington, DC 20460–0001; telephone
number: (202) 564–8089; email address:
calvo.kathy@epa.gov.
For general information contact: The
TSCA-Hotline, ABVI-Goodwill, 422
South Clinton Ave., Rochester, NY
14620; telephone number: (202) 554–
1404; email address: TSCA-Hotline@
epa.gov.
SUPPLEMENTARY INFORMATION:
I. Chemical Substances and/or Mixtures
Information about the following
chemical substances and/or mixtures is
provided in Unit IV.: 1,3-Propanediol,
2,2-bis[(nitrooxy)methyl]-, dinitrate
(ester) (78–11–5).
II. Federal Register Publication
Requirement
Section 4(d) of TSCA (15 U.S.C.
2603(d)) requires EPA to publish a
notice in the Federal Register reporting
the receipt of test data submitted
pursuant to test rules promulgated
under TSCA section 4 (15 U.S.C. 2603).
III. Docket Information
A docket, identified by the docket
identification (ID) number EPA–HQ–
OPPT–2013–0677, has been established
for this Federal Register document that
announces the receipt of data. Upon
EPA’s completion of its quality
assurance review, the test data received
will be added to the docket for the
TSCA section 4 test rule that required
the test data. Use the docket ID number
provided in Unit IV. to access the test
data in the docket for the related TSCA
section 4 test rule.
The docket for this Federal Register
document and the docket for each
related TSCA section 4 test rule is
available electronically at https://
www.regulations.gov or in person at the
Office of Pollution Prevention and
Toxics Docket (OPPT Docket),
Environmental Protection Agency
Docket Center (EPA/DC), West William
Jefferson Clinton Bldg., Rm. 3334, 1301
Constitution Ave. NW., Washington,
DC. 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 OPPT
E:\FR\FM\25MRN1.SGM
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Agencies
[Federal Register Volume 80, Number 57 (Wednesday, March 25, 2015)]
[Notices]
[Pages 15785-15787]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2015-06860]
=======================================================================
-----------------------------------------------------------------------
ENVIRONMENTAL PROTECTION AGENCY
[EPA-HQ-OPP-2015-0059; FRL-9923-76]
Registration Review Proposed Interim Decisions; Notice of
Availability
AGENCY: Environmental Protection Agency (EPA).
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: This notice announces the availability of EPA's proposed
interim registration review decisions on certain pesticides and opens a
public comment period on the proposed interim decisions. 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.March 25, 2015
DATES: Comments must be received on or before May 26, 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., 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.
[[Page 15786]]
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.
Table--Registration Review Proposed Interim Decisions
------------------------------------------------------------------------
Chemical review
Registration review case name Pesticide Docket manager, telephone
and No. ID No. No., email address
------------------------------------------------------------------------
Debacarb (2-EEEBC) (Case 4031) EPA-HQ-OPP-2008-0 Roy Johnson, 703-347-
802. 0492,
johnson.roy@epa.gov.
Maleic Hydrazide (Case 0381).. EPA-HQ-OPP-2009-0 Ricardo Jones, 703-
387. 347-0493,
jones.ricardo@epa.gov.
Soap Salts (Case 4083)........ EPA-HQ-OPP-2008-0 Eric Miederhoff, 703-
519. 347-8028
miederhoff.eric@epa.gov.
------------------------------------------------------------------------
Debacarb (2-EEEBC) (Proposed Interim Decision). Debacarb is a
fungicide registered for use to control certain diseases in ornamental
trees. The fungicide is applied to mature trees by injection through
the trunk. EPA has completed a draft ecological risk assessment,
including a screening-level listed species assessment. A human health
risk assessment is not needed because the method of application limits
the possibility for applicator or other human exposure. Direct adverse
effects are not expected for birds, reptiles, terrestrial-phase
amphibians, mammals, and terrestrial plants. The Agency has made a No
Effects (NE) determination for all federally-listed species within
these groups and a No Habitat Modification determination for all
designated critical habitats associated with these species for the
currently registered uses of debacarb. Risks currently cannot be
precluded for aquatic receptors and terrestrial invertebrates. At this
time, to eliminate uncertainty and reduce potential risks to non-listed
aquatic species, the Agency is proposing restrictions on application to
trees near waterbodies. To reduce uncertainty and potential risks to
insect pollinators, the Agency is proposing that applications to trees
be limited to the post-bloom period. This proposed interim decision
does not cover the Endocrine Disruptor Screening program (EDSP)
component of this registration review case, nor does it provide a
complete Endangered Species assessment (ESA) for debacarb. However,
pending the outcome of this action, the EPA is planning to issue an
interim registration review decision for debacarb.
Maleic Hydrazide (Proposed Interim Decision). The registration
review docket for maleic hydrazide (EPA-HQ-OPP-2009-0387) opened in
September 2009. Maleic hydrazide is a systemic plant growth regulator
registered for use on tobacco, potato, onions, non-bearing citrus,
turf, utility and highway rights-of-way, airports, industrial land,
lawns, recreational areas, ornamental/shade trees and ornamental
plants. Uses include residential use on turf and lawns as a perimeter
or spot treatment. EPA published draft human health and ecological risk
assessments in July 2014. No human health risks of concern were
identified. The Agency also completed an ecological risk assessment.
The results of this quantitative risk assessment indicates that the
currently labeled rates of maleic hydrazide pose a potential for risk
to non-target terrestrial birds and terrestrial invertebrates. In
addition, applications may impact sensitive species of semi-aquatic and
terrestrial monocotyledonous plants (monocots). The Agency completed a
screening-level ESA and made a ``no effects'' determination for the
following taxa: Aquatic plants and aquatic freshwater and estuarine/
marine organisms. For all other species applications ``may affect'' or
are uncertain. Maleic hydrazide has not been evaluated under the EDSP
nor has it completed ESA section 7 consultation with the U.S. Fish and
Wildlife Service and the National Marine and Fisheries Service
(Services). Therefore, the Agency's final registration review decision
is dependent upon the result of the evaluation of potential endocrine
disruptor risk and consultation with the Services for endangered
species. Pending the outcome of this action, the EPA is planning to
issue an interim registration review decision for maleic hydrazide.
Soap Salts (Proposed Interim Decision). The registration review
docket for soap salts (EPA-HQ-OPP-2008-0519) opened in September 2008.
Soap Salts are used as acaricides, herbicides, and insecticides on food
and non-food crops in various settings, chiefly residential and
agricultural. Ammonium and sodium soap salts are also used as animal
repellants. EPA published draft human health and ecological risk
assessments in March 2013. EPA conducted a human health risk assessment
and did not identify any risks of concern. No human health mitigation
is being proposed by the Agency for the soap salts at this time. The
Agency also conducted an ecological risk assessment for the current
uses of the soap salts. The screening-level risk assessment did find
the potential for minor risk to terrestrial plants and aquatic
organisms from the use of potassium and ammonium salts. However, the
Agency believes there is little actual risk to non-target plants
exposed to soap salts due to the rapid degradation of soap salts in
surface water runoff, which was not accounted for in the risk
assessment model, and the inherent insolubility and low toxicity of the
soap salts. Therefore, the Agency has no risk concerns from the
terrestrial or aquatic assessments and is
[[Page 15787]]
not proposing ecological risk mitigation at this time. The Agency also
completed a screening-level endangered and threatened (listed) species
assessment for soap salts and identified potential risks to several
taxa: Freshwater invertebrates, estuarine/marine invertebrates, and
terrestrial plants. However, at this time in registration review, it is
premature to make an endangered species effects determination for
federally listed species and their designated critical habitats under
ESA. Also, the soap salts have not yet been evaluated under the EDSP.
Therefore, the Agency's final registration review decision is dependent
upon the results of the evaluation of risks to threatened and
endangered species and of potential endocrine disruptor risk. Pending
the outcome of this action, the EPA is planning to issue an interim
registration review decision for the soap salts.
The registration review docket for a pesticide includes earlier
documents related to the registration review of the case. For example,
the review opened with a Summary Document, containing a Preliminary
Work Plan, for public comment. A Final Work Plan was placed in the
docket following public comment on the initial docket. The documents in
the docket describe EPA's rationales for conducting additional risk
assessments, as well as the Agency's subsequent risk findings and
consideration of possible risk mitigation measures. A proposed interim
registration review decision is supported by the rationales included in
those documents. Following public comment on a proposed decision, the
Agency will issue interim registration review decisions for products
containing the pesticides listed in the table in Unit II.
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 August 2006 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 decision. 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 required to consider these late
comments.
The Agency will carefully consider all comments received by the
closing date and will provide a ``Response to Comments Memorandum'' in
the docket as appropriate. The final registration review decision will
explain the effect that any comments had on the decision.
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 these pesticides are provided at:
https://www.epa.gov/oppsrrd1/registration_review/reg_review_status.htm.
Authority: 7 U.S.C. 136 et seq.
Dated: March 17, 2015.
Richard P. Keigwin, Jr.,
Director, Pesticide Re-Evaluation Division, Office of Pesticide
Programs.
[FR Doc. 2015-06860 Filed 3-24-15; 8:45 am]
BILLING CODE 6560-50-P