Mefluidide Risk Assessments; Notice of Availability, 34007-34009 [E7-11943]
Download as PDF
Federal Register / Vol. 72, No. 118 / Wednesday, June 20, 2007 / Notices
I. General Information
List of Subjects
A. Does this Action Apply to Me?
Environmental protection, Fumigants,
Pesticides and pests.
The Agency included in the notices of
May 2, 2007, a list of those who may be
potentially affected by this action. If you
have questions regarding the
applicability of this action to a
particular entity, consult the person
listed under FOR FURTHER INFORMATION
CONTACT in the Federal Register
documents of May 2, 2007.
Dated: June 13, 2007.
Peter Caulkins,
Acting Director, Special Review and
Reregistration Division, Office of Pesticide
Programs.
[FR Doc. E7–11796 Filed 6–19–07; 8:45 am]
BILLING CODE 6560–50–S
B. How Can I Access Electronic Copies
of this Document?
ENVIRONMENTAL PROTECTION
AGENCY
In addition to accessing an electronic
copy of this Federal Register document
through the electronic docket athttps://
www.regulations.gov, you may access
this Federal Register document
electronically through the EPA Internet
under the ‘‘Federal Register’’ listings at
https://www.epa.gov/fedrgstr.
[EPA–HQ–OPP–2007–0431; FRL–8135–4]
II. What Action is EPA taking?
This document extends the public
comment periods for the fumigants
chloropicrin, dazomet, 1,3dichloropropene, metam potassium,
metam sodium, and methyl bromide
established in the Federal Register
issued on May 2, 2007 (72 FR 24290,
FRL–8127–7), (72 FR 24292, FRL–8126–
7), (72 FR 24294, FRL–8124–8), (72 FR
24295, FRL–8125–9), and (72 FR 24297,
FRL–8125–7). In those documents, EPA
announced the availability of the risk
assessments and opened 60–day public
comment periods. EPA is hereby
extending the comment periods, which
were set to end on July 2, 2007 to
September 3, 2007.
rwilkins on PROD1PC63 with NOTICES
III. What is the Agency’s Authority for
Taking this Action?
Section 4(g)(2) of the Federal
Insecticide, Fungicide, and Rodenticide
Act (FIFRA), as amended, directs that,
after submission of all data concerning
a pesticide active ingredient, the
Administrator shall determine whether
pesticides containing such active
ingredient are eligible for reregistration.
Further provisions are made to allow a
public comment period. However, the
Administrator may extend the comment
period if additional time for comment is
requested. In this case, Grimmway
Farms; Certis U.S.A., L.L.C; Washington
Minor Crops Association; Washington
State Potato Commission; Amalgamated
Sugar Company; Methyl Bromide
Industry Task Force; the Idaho Potato
Growers Association; and other
individuals have requested additional
time to develop comments. The Agency
believes that an additional 60 days is
warranted.
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Mefluidide Risk Assessments; Notice
of Availability
Environmental Protection
Agency (EPA).
ACTION: Notice.
AGENCY:
SUMMARY: This notice announces the
availability of EPA’s risk assessments,
and related documents for the pesticide
mefluidide, and opens a public
comment period on these documents.
The public is encouraged to suggest risk
management ideas or proposals to
address the risks identified. EPA is
developing a Reregistration Eligibility
Decision (RED) for mefluidide through a
modified, 4-Phase public participation
process that the Agency uses to involve
the public in developing pesticide
reregistration decisions. This is Phase 3
of the process. Through this program,
EPA is ensuring that all pesticides meet
current health and safety standards.
DATES: Comments must be received on
or before August 20, 2007.
ADDRESSES: Submit your comments,
identified by docket identification (ID)
number EPA–HQ–OPP–2007–0431, by
one of the following methods:
• Federal eRulemaking Portal: https://
www.regulations.gov. Follow the on-line
instructions for submitting comments.
• Mail: Office of Pesticide Programs
(OPP) Regulatory Public Docket (7502P),
Environmental Protection Agency, 1200
Pennsylvania Ave., NW., Washington,
DC 20460–0001.
• Delivery: OPP Regulatory Public
Docket (7502P), Environmental
Protection Agency, Rm. S–4400, One
Potomac Yard (South Building), 2777 S.
Crystal Drive, Arlington, VA. Deliveries
are only accepted during the Docket’s
normal hours of operation (8:30 a.m. to
4 p.m., Monday through Friday,
excluding legal holidays). Special
arrangements should be made for
deliveries of boxed information. The
Docket telephone number is (703) 305–
5805.
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34007
Instructions: Direct your comments to
docket ID number EPA–HQ–OPP–2007–
0431. EPA’s policy is that all comments
received will be included in the docket
without change and may be made
available on-line at https://
www.regulations.gov, including any
personal information provided, unless
the comment includes information
claimed to be Confidential Business
Information (CBI) or other information
whose disclosure is restricted by statute.
Do not submit information that you
consider to be CBI or otherwise
protected through regulations.gov or email. The Federal regulations.gov
website is an ‘‘anonymous access’’
system, which means EPA will not
know your identity or contact
information unless you provide it in the
body of your comment. If you send an
e-mail comment directly to EPA without
going through regulations.gov, your email address will be automatically
captured and included as part of the
comment that is placed in the docket
and made available on the Internet. If
you submit an electronic comment, EPA
recommends that you include your
name and other contact information in
the body of your comment and with any
disk or CD-ROM you submit. If EPA
cannot read your comment due to
technical difficulties and cannot contact
you for clarification, EPA may not be
able to consider your comment.
Electronic files should avoid the use of
special characters, any form of
encryption, and be free of any defects or
viruses.
Docket: All documents in the docket
are listed in the docket index available
in regulations.gov. To access the
electronic docket, go to https://
www.regulations.gov, select ‘‘Advanced
Search,’’ then ‘‘Docket Search.’’ Insert
the docket ID number where indicated
and select the ‘‘Submit’’ button. Follow
the instructions on the regulations.gov
web site to view the docket index or
access available documents. Although
listed in the index, some information is
not publicly available, e.g., CBI or other
information whose disclosure is
restricted by statute. Certain other
material, such as copyrighted material,
is not placed on the Internet and will be
publicly available only in hard copy
form. Publicly available docket
materials are available either in the
electronic docket at https://
www.regulations.gov, or, if only
available in hard copy, at the OPP
Regulatory Public Docket in Rm. S–
4400, One Potomac Yard (South
Building), 2777 S. Crystal Drive,
Arlington, VA. The hours of operation
of this Docket Facility are from 8:30 a.m.
E:\FR\FM\20JNN1.SGM
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34008
Federal Register / Vol. 72, No. 118 / Wednesday, June 20, 2007 / Notices
to 4 p.m., Monday through Friday,
excluding legal holidays. The Docket
telephone number is (703) 305–5805.
FOR FURTHER INFORMATION CONTACT:
Wilhelmena Livingston, Special Review
and Reregistration Division (7508P),
Office of Pesticide Programs,
Environmental Protection Agency, 1200
Pennsylvania Ave., NW., Washington,
DC 20460–0001; telephone number: 703
308–8025; fax number: (703) 308–8005;
e-mail address:
livingston.wilhelmena@epa.gov.
SUPPLEMENTARY INFORMATION:
I. General Information
rwilkins on PROD1PC63 with NOTICES
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, 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 person
listed under FOR FURTHER INFORMATION
CONTACT.
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 e-mail. 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 submitting comments, remember
to:
i. Identify the document by docket ID
number and other identifying
information (subject heading, Federal
Register date and page number).
ii. Follow directions. The Agency may
ask you to respond to specific questions
or organize comments by referencing a
Code of Federal Regulations (CFR) part
or section number.
VerDate Aug<31>2005
18:25 Jun 19, 2007
Jkt 211001
iii. Explain why you agree or disagree;
suggest alternatives and substitute
language for your requested changes.
iv. Describe any assumptions and
provide any technical information and/
or data that you used.
v. If you estimate potential costs or
burdens, explain how you arrived at
your estimate in sufficient detail to
allow for it to be reproduced.
vi. Provide specific examples to
illustrate your concerns and suggest
alternatives.
vii. Explain your views as clearly as
possible, avoiding the use of profanity
or personal threats.
viii. Make sure to submit your
comments by the comment period
deadline identified.
II. Background
A. What Action is the Agency Taking?
EPA is releasing for public comment
its human health and environmental
fate and effects risk assessments and
related documents for mefluidide, and
soliciting public comment on risk
management ideas or proposals.
Mefluidide is a plant growth regulator
that is applied postemergence when
needed. EPA developed the risk
assessments and risk characterization
for mefluidide through a modified
version of its public process for making
pesticide reregistration eligibility and
tolerance reassessment decisions.
Through these programs, EPA is
ensuring that pesticides meet current
standards under the Federal Insecticide,
Fungicide, and Rodenticide Act (FIFRA)
and the Federal Food, Drug, and
Cosmetic Act (FFDCA), as amended by
the Food Quality Protection Act of 1996
(FQPA).
Mefluidide is a plant growth regulator
that is applied postemergence when
needed. It is used to control ornamental
and non-ornamental woody plants,
ground cover, hedges trees, turf grasses,
grass and broadleaf weeds by inhibiting
plant cell division, stem elongation and
seed head development. It is also
registered for growth control of low
maintenance turf on rights-of way,
airports, public and industrial sites.
Mefluidide products can also be used on
residential lawns.
EPA is providing an opportunity,
through this notice, for interested
parties to provide comments and input
on the Agency’s risk assessments for
mefluidide. Such comments and input
could address, for example, the
availability of additional data to further
refine the risk assessments, such as
usage/use information for nonagricultural uses, or could address the
Agency’s risk assessment methodologies
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and assumptions as applied to this
specific pesticide.
Through this notice, EPA also is
providing an opportunity for interested
parties to provide risk management
proposals or otherwise comment on risk
management for mefluidide. Risks of
concern associated with the use of
mefluidide are: Acute (listed and nonlisted) and chronic risks to mammals
and birds, as well as acute (listed and
non-listed) risk to terrestrial and semiaquatic plants from use on ornamental
turf. In targeting these risks of concern,
the Agency solicits information on
effective and practical risk reduction
measures.
EPA seeks to achieve environmental
justice, the fair treatment and
meaningful involvement of all people,
regardless of race, color, national origin,
or income, 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, unusually high exposure to
mefluidide, compared to the general
population.
EPA is applying the principles of
public participation to all pesticides
undergoing reregistration and tolerance
reassessment. The Agency’s Pesticide
Tolerance Reassessment and
Reregistration; Public Participation
Process, published in the Federal
Register on May 14, 2004 (69 FR 26819)
(FRL–7357–9), explains that in
conducting these programs, the Agency
is tailoring its public participation
process to be commensurate with the
level of risk, extent of use, complexity
of the issues, and degree of public
concern associated with each pesticide.
For mefluidide, a modified, 4-Phase
process with one comment period and
ample opportunity for public
consultation seems appropriate in view
of its few complex issues. However, if
as a result of comments received during
this comment period EPA finds that
additional issues warranting further
discussion are raised, the Agency may
lengthen the process and include a
second comment period, as needed.
All comments should be submitted
using the methods in ADDRESSES, and
must be received by EPA on or before
the closing date. Comments will become
part of the Agency Docket for
mefluidide. Comments received after
the close of the comment period will be
marked ‘‘late.’’ EPA is not required to
consider these late comments.
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Federal Register / Vol. 72, No. 118 / Wednesday, June 20, 2007 / Notices
B. What is the Agency’s Authority for
Taking this Action?
Section 4(g)(2) of FIFRA as amended
directs that, after submission of all data
concerning a pesticide active ingredient,
‘‘the Administrator shall determine
whether pesticides containing such
active ingredient are eligible for
reregistration,’’ before calling in
product-specific data on individual enduse products and either reregistering
products or taking other ‘‘appropriate
regulatory action.’’
List of Subjects
Environmental protection, Pesticides
and pests.
Dated: June 12, 2007.
Peter Caulkins,
Acting Director, Special Review and
Reregistration Division, Office of Pesticide
Programs.
[FR Doc. E7–11943 Filed 6–19–07; 8:45 am]
BILLING CODE 6560–50–S
B. How Can I Get Copies of this
Document and Other Related
Information?
1. Docket. EPA has established a
docket for this action under docket
identification (ID) number EPA–HQ–
OPP–2007–0179. Publicly available
docket materials are available either in
the electronic docket at https://
www.regulations.gov, or, if only
available in hard copy, at the Office of
Pesticide Programs (OPP) Regulatory
Public Docket in Rm. S–4400, One
Potomac Yard (South Bldg.), 2777 S.
Crystal Dr., Arlington, VA. The hours of
operation of this Docket Facility are
from 8:30 a.m. to 4 p.m., Monday
through Friday, excluding legal
holidays. The Docket Facility telephone
number is (703) 305–5805.
2. Electronic access. You may access
this Federal Register document
electronically through the EPA Internet
under the ‘‘Federal Register’’ listings at
https://www.epa.gov/fedrgstr.
II. EUPs
ENVIRONMENTAL PROTECTION
AGENCY
[EPA–HQ–OPP–2007–0179; FRL–8133–5]
Issuance of Experimental Use Permits
Environmental Protection
Agency (EPA).
ACTION: Notice.
AGENCY:
SUMMARY: EPA has granted experimental
use permits (EUPs) to the following
pesticide applicants. An EUP permits
use of a pesticide for experimental or
research purposes only in accordance
with the limitations in the permit.
FOR FURTHER INFORMATION CONTACT:
Alan Reynolds, Biopesticides and
Pollution Prevention Division (7511P),
Office of Pesticide Programs,
Environmental Protection Agency, 1200
Pennsylvania Ave., NW., Washington,
DC 20460–0001; telephone number:
(703) 605–0515; e-mail address:
reynolds.alan@epa.gov.
SUPPLEMENTARY INFORMATION:
I. General Information
rwilkins on PROD1PC63 with NOTICES
A. Does this Action Apply to Me?
This action is directed to the public
in general. Although this action may be
of particular interest to those persons
who conduct or sponsor research on
pesticides, 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 information in this action,
consult the person listed under FOR
FURTHER INFORMATION CONTACT.
VerDate Aug<31>2005
18:25 Jun 19, 2007
Jkt 211001
EPA has issued the following EUPs:
264–EUP–140. Extension. Bayer
CropScience LP, 2. T.W. Alexander
Drive, Research Triangle Park, NC
27709. This EUP allows the use of 1,008
pounds of cotton seed containing the
following plant incorporated protectant
(PIP) in the amount specified: 0.016
pounds of Cry1Ab protein and the
genetic material necessary for its
production (vector pTDL004) in Events
T303–3 and T304–40 cotton. This EUP
allows the use of this seed on 84 acres
of Events T303–3 and T304–40 cotton.
Four trial protocols will be conducted,
including:
• Efficacy testing.
• Agronomic evaluation.
• Dissemination of pollen evaluation.
• Production of sample material for
use in regulatory studies.
The program is authorized only in the
States of Arizona, California, Georgia,
Louisiana, Mississippi, North Carolina,
South Carolina, and Texas. The EUP is
effective from March 8, 2007 to May 1,
2008.
An exemption from tolerance has
been established for residues of the
active ingredient in or on all cotton
commodities. One comment was
received from a private citizen in
response to the notice of receipt for this
permit application, which was
published in the Federal Register on
January 17, 2007 (72 FR 1993) (FRL–
8105–7). The private citizen indicated
that she opposed testing under this EUP
except in fully enclosed greenhouses,
and expressed the viewpoint that the
permittee should be required to request
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34009
permission from neighbors prior to
testing. The Agency understands the
commenter’s concerns. Under the
Federal Insecticide, Fungicide, and
Rodenticide Act (FIFRA), the Agency is
tasked with reviewing applications for
EUPs for any pesticide, including PIPs,
and granting such applications to the
extent that the conditions of FIFRA
section 5, and the regulations
thereunder, have been met (subject to
such terms and conditions as the
Agency determines are warranted). In
this instance, EPA has determined that
the relevant statutory and regulatory
conditions have been met. In addition,
there is nothing in FIFRA or in the
Agency’s regulations enacted
thereunder that compels, and EPA does
not otherwise require, a permittee to
notify neighbors prior to testing as
suggested. Finally, although certain
containment provisions were required
per the experimental program, the
Agency did not require testing to be
conducted in fully enclosed
greenhouses because such a requirement
was not necessary to mitigate risk.
67979–EUP–6. Issuance. Syngenta
Seeds, Inc., P.O. Box 12257, Research
Triangle Park, NC 27709. This EUP
allows the use of 62,173 pounds of corn
seed containing the following plant
incorporated protectants (PIPs) in the
amounts specified: 0.916 pounds of
Vip3Aa20 protein and the genetic
material necessary for its production
(vector pNOV1300) in Event MIR 162
corn, 0.046 pounds of Cry1Ab protein
and the genetic material necessary for
its production (vector pZO1502) in
Event Bt11 corn, and 0.013 pounds of
mCry3A protein and the genetic
material necessary for its production
(vector pZM26) in Event MIR 604 corn.
This EUP allows the use of this seed on
536 acres of MIR 162 corn; 220 acres of
Bt11 corn; 199 acres of MIR 604 corn;
469 acres of Bt11 x MIR 162 corn; and
468 acres of Bt11 x MIR 162 x MIR 604
corn for 2007–2008. Five trial protocols
will be conducted, including:
• Breeding and observation.
• Insect efficacy.
• Agronomic evaluation.
• Inbred and hybrid seed production.
• Regulatory studies.
The program is authorized only in the
States of California, Colorado, Florida,
Georgia, Hawaii, Idaho, Illinois, Indiana,
Iowa, Kansas, Kentucky, Louisiana,
Maryland, Minnesota, Mississippi,
Missouri, Nebraska, New York, Ohio,
Puerto Rico, South Dakota, Texas, and
Wisconsin. The EUP is effective from
March 21, 2007 to March 31, 2008.
Permanent or temporary exemptions
from tolerance have been established for
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Agencies
[Federal Register Volume 72, Number 118 (Wednesday, June 20, 2007)]
[Notices]
[Pages 34007-34009]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E7-11943]
-----------------------------------------------------------------------
ENVIRONMENTAL PROTECTION AGENCY
[EPA-HQ-OPP-2007-0431; FRL-8135-4]
Mefluidide Risk Assessments; Notice of Availability
AGENCY: Environmental Protection Agency (EPA).
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: This notice announces the availability of EPA's risk
assessments, and related documents for the pesticide mefluidide, and
opens a public comment period on these documents. The public is
encouraged to suggest risk management ideas or proposals to address the
risks identified. EPA is developing a Reregistration Eligibility
Decision (RED) for mefluidide through a modified, 4-Phase public
participation process that the Agency uses to involve the public in
developing pesticide reregistration decisions. This is Phase 3 of the
process. Through this program, EPA is ensuring that all pesticides meet
current health and safety standards.
DATES: Comments must be received on or before August 20, 2007.
ADDRESSES: Submit your comments, identified by docket identification
(ID) number EPA-HQ-OPP-2007-0431, by one of the following methods:
Federal eRulemaking Portal: https://www.regulations.gov.
Follow the on-line instructions for submitting comments.
Mail: Office of Pesticide Programs (OPP) Regulatory Public
Docket (7502P), Environmental Protection Agency, 1200 Pennsylvania
Ave., NW., Washington, DC 20460-0001.
Delivery: OPP Regulatory Public Docket (7502P),
Environmental Protection Agency, Rm. S-4400, One Potomac Yard (South
Building), 2777 S. Crystal Drive, Arlington, VA. Deliveries are only
accepted during the Docket's normal hours of operation (8:30 a.m. to 4
p.m., Monday through Friday, excluding legal holidays). Special
arrangements should be made for deliveries of boxed information. The
Docket telephone number is (703) 305-5805.
Instructions: Direct your comments to docket ID number EPA-HQ-OPP-
2007-0431. EPA's policy is that all comments received will be included
in the docket without change and may be made available on-line at
https://www.regulations.gov, including any personal information
provided, unless the comment includes information claimed to be
Confidential Business Information (CBI) or other information whose
disclosure is restricted by statute. Do not submit information that you
consider to be CBI or otherwise protected through regulations.gov or e-
mail. The Federal regulations.gov website is an ``anonymous access''
system, which means EPA will not know your identity or contact
information unless you provide it in the body of your comment. If you
send an e-mail comment directly to EPA without going through
regulations.gov, your e-mail address will be automatically captured and
included as part of the comment that is placed in the docket and made
available on the Internet. If you submit an electronic comment, EPA
recommends that you include your name and other contact information in
the body of your comment and with any disk or CD-ROM you submit. If EPA
cannot read your comment due to technical difficulties and cannot
contact you for clarification, EPA may not be able to consider your
comment. Electronic files should avoid the use of special characters,
any form of encryption, and be free of any defects or viruses.
Docket: All documents in the docket are listed in the docket index
available in regulations.gov. To access the electronic docket, go to
https://www.regulations.gov, select ``Advanced Search,'' then ``Docket
Search.'' Insert the docket ID number where indicated and select the
``Submit'' button. Follow the instructions on the regulations.gov web
site to view the docket index or access available documents. Although
listed in the index, some information is not publicly available, e.g.,
CBI or other information whose disclosure is restricted by statute.
Certain other material, such as copyrighted material, is not placed on
the Internet and will be publicly available only in hard copy form.
Publicly available docket materials are available either in the
electronic docket at https://www.regulations.gov, or, if only available
in hard copy, at the OPP Regulatory Public Docket in Rm. S-4400, One
Potomac Yard (South Building), 2777 S. Crystal Drive, Arlington, VA.
The hours of operation of this Docket Facility are from 8:30 a.m.
[[Page 34008]]
to 4 p.m., Monday through Friday, excluding legal holidays. The Docket
telephone number is (703) 305-5805.
FOR FURTHER INFORMATION CONTACT: Wilhelmena Livingston, Special Review
and Reregistration Division (7508P), Office of Pesticide Programs,
Environmental Protection Agency, 1200 Pennsylvania Ave., NW.,
Washington, DC 20460-0001; telephone number: 703 308-8025; fax number:
(703) 308-8005; e-mail address: livingston.wilhelmena@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, 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 person
listed under FOR FURTHER INFORMATION CONTACT.
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 e-mail. 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 submitting comments,
remember to:
i. Identify the document by docket ID number and other identifying
information (subject heading, Federal Register date and page number).
ii. Follow directions. The Agency may ask you to respond to
specific questions or organize comments by referencing a Code of
Federal Regulations (CFR) part or section number.
iii. Explain why you agree or disagree; suggest alternatives and
substitute language for your requested changes.
iv. Describe any assumptions and provide any technical information
and/or data that you used.
v. If you estimate potential costs or burdens, explain how you
arrived at your estimate in sufficient detail to allow for it to be
reproduced.
vi. Provide specific examples to illustrate your concerns and
suggest alternatives.
vii. Explain your views as clearly as possible, avoiding the use of
profanity or personal threats.
viii. Make sure to submit your comments by the comment period
deadline identified.
II. Background
A. What Action is the Agency Taking?
EPA is releasing for public comment its human health and
environmental fate and effects risk assessments and related documents
for mefluidide, and soliciting public comment on risk management ideas
or proposals. Mefluidide is a plant growth regulator that is applied
postemergence when needed. EPA developed the risk assessments and risk
characterization for mefluidide through a modified version of its
public process for making pesticide reregistration eligibility and
tolerance reassessment decisions. Through these programs, EPA is
ensuring that pesticides meet current standards under the Federal
Insecticide, Fungicide, and Rodenticide Act (FIFRA) and the Federal
Food, Drug, and Cosmetic Act (FFDCA), as amended by the Food Quality
Protection Act of 1996 (FQPA).
Mefluidide is a plant growth regulator that is applied
postemergence when needed. It is used to control ornamental and non-
ornamental woody plants, ground cover, hedges trees, turf grasses,
grass and broadleaf weeds by inhibiting plant cell division, stem
elongation and seed head development. It is also registered for growth
control of low maintenance turf on rights-of way, airports, public and
industrial sites. Mefluidide products can also be used on residential
lawns.
EPA is providing an opportunity, through this notice, for
interested parties to provide comments and input on the Agency's risk
assessments for mefluidide. Such comments and input could address, for
example, the availability of additional data to further refine the risk
assessments, such as usage/use information for non-agricultural uses,
or could address the Agency's risk assessment methodologies and
assumptions as applied to this specific pesticide.
Through this notice, EPA also is providing an opportunity for
interested parties to provide risk management proposals or otherwise
comment on risk management for mefluidide. Risks of concern associated
with the use of mefluidide are: Acute (listed and non-listed) and
chronic risks to mammals and birds, as well as acute (listed and non-
listed) risk to terrestrial and semi-aquatic plants from use on
ornamental turf. In targeting these risks of concern, the Agency
solicits information on effective and practical risk reduction
measures.
EPA seeks to achieve environmental justice, the fair treatment and
meaningful involvement of all people, regardless of race, color,
national origin, or income, 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, unusually high exposure to mefluidide, compared to the
general population.
EPA is applying the principles of public participation to all
pesticides undergoing reregistration and tolerance reassessment. The
Agency's Pesticide Tolerance Reassessment and Reregistration; Public
Participation Process, published in the Federal Register on May 14,
2004 (69 FR 26819) (FRL-7357-9), explains that in conducting these
programs, the Agency is tailoring its public participation process to
be commensurate with the level of risk, extent of use, complexity of
the issues, and degree of public concern associated with each
pesticide. For mefluidide, a modified, 4-Phase process with one comment
period and ample opportunity for public consultation seems appropriate
in view of its few complex issues. However, if as a result of comments
received during this comment period EPA finds that additional issues
warranting further discussion are raised, the Agency may lengthen the
process and include a second comment period, as needed.
All comments should be submitted using the methods in ADDRESSES,
and must be received by EPA on or before the closing date. Comments
will become part of the Agency Docket for mefluidide. Comments received
after the close of the comment period will be marked ``late.'' EPA is
not required to consider these late comments.
[[Page 34009]]
B. What is the Agency's Authority for Taking this Action?
Section 4(g)(2) of FIFRA as amended directs that, after submission
of all data concerning a pesticide active ingredient, ``the
Administrator shall determine whether pesticides containing such active
ingredient are eligible for reregistration,'' before calling in
product-specific data on individual end-use products and either
reregistering products or taking other ``appropriate regulatory
action.''
List of Subjects
Environmental protection, Pesticides and pests.
Dated: June 12, 2007.
Peter Caulkins,
Acting Director, Special Review and Reregistration Division, Office of
Pesticide Programs.
[FR Doc. E7-11943 Filed 6-19-07; 8:45 am]
BILLING CODE 6560-50-S