Experimental Use Permit; Receipt of Amendment Application, 5561-5563 [E8-1412]
Download as PDF
Federal Register / Vol. 73, No. 20 / Wednesday, January 30, 2008 / Notices
E. Is the proposed collection consistent
with and compatible with the
respondent’s current reporting and
recordkeeping practices to the
maximum extent practicable?
The proposed information collection
is voluntary. Western proposes to use
the information to determine whether
an applicant qualifies as a preference
entity to receive an allocation of Federal
power. As discussed above, there is no
mandatory recordkeeping requirement
on the applicant if it does not receive an
allocation of Federal power. For those
entities that receive a Federal power
allocation, Western proposes a
requirement that they keep the
information for 3 years after Western
grants the power allocation and the
applicant signs a Federal power
contract. The proposed 3-year record
retention policy for such applicants
would allow Western sufficient time to
administer the contract and to ensure
the applicant provided factual
information in its application. Western
anticipates that a 3-year record retention
policy will have little impact on most
businesses in the power industry who
will keep the APD as part of their
normal business records. The procedure
and process for the allocation of power
shall be the subject matter of a separate
notice and is outside the scope of this
process.
F. Does the proposed collection indicate
the retention period for any
recordkeeping requirements for the
respondent?
The APD identifies that there is no
recordkeeping requirement for the
respondent if it does not receive an
allocation of Federal power. It also
identifies that applicants who receive an
allocation of Federal power must retain
the records for 3 years.
mstockstill on PROD1PC66 with NOTICES
G. Does the proposed collection inform
the public of the information they need
to exercise scrutiny of the agency
collecting information (the reasons the
proposed information is collected, the
way it is used, an estimate of the
burden, whether the response is
voluntary, required to obtain a benefit,
or mandatory and a statement that no
person is required to respond unless a
valid OMB control number is
displayed)?
If an entity desires a Federal power
allocation from Western, Western needs
certain information to determine
whether the entity is eligible to receive
power. Western has a limited amount of
power available. Western uses its
discretion in allocating power. In order
to use its discretion in allocating power,
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18:49 Jan 29, 2008
Jkt 214001
Western will use the information
collected on the application. Western
will not accept incomplete applications.
Western will work with Native
American Tribes and other entities who
may need assistance in filling out the
application. No person is required to
submit any information unless a valid
OMB control number is displayed. No
person is required to submit any
information unless they desire a Federal
power allocation.
H. Is the proposed collection developed
by an office that has planned and
allocated resources for the efficient and
effective management and use of the
information collected?
Western’s power marketing offices
will administer and evaluate the
applications. Use and management of
the collected information has been
factored into these offices functions and
resource requirements. Historically,
Western has requested the same relative
information from applicants in past
marketing plan initiatives and
effectively utilized Western resources to
utilize and manage the information in
its determinations. The power
marketing offices will make a
recommendation to Western’s
Administrator on which applicant(s)
should be awarded a Federal power
allocation based on the information
contained in the APD. Western’s
Administrator shall use his discretion in
the final power allocations. The
procedure and process for the allocation
of power shall be the subject matter of
a separate notice and is outside the
scope of this process.
I. Does the proposed collection use
effective and efficient statistical survey
methods?
Since the proposed information
collected is used to determine whether
an applicant receives an allocation of
Federal power, this section is
inapplicable.
J. Does the proposed collection use
information technology to the maximum
extent practicable to reduce the burden
and to improve data quality, agency
efficiency, and responsiveness to the
public?
The APD will be accessible for
downloading via Western’s Web site.
Western will accept electronic-mail
submission of the APD, as well as
submission via fax or regular mail.
Applicants cannot enter the information
on Western’s Web site.
VI. Invitation for Comments
Western invites public comment on a
proposed collection of information that
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Sfmt 4703
5561
Western is developing for submission to
OMB pursuant to the Paperwork
Reduction Act of 1995. Comments are
invited on: (1) Whether the proposed
collection of information is necessary
for the proper performance of the
functions of the agency, including
whether the information shall have
practical utility; (2) the accuracy of the
agency’s estimate of the burden of the
proposed collection of information,
including the validity of the
methodology and assumptions used; (3)
ways to enhance the quality, utility, and
clarity of the information to be
collected; and (4) ways to minimize the
burden of the collection of information
on respondents, including through the
use of automated collection techniques
or other forms of information
technology.
Dated: January 3, 2008.
Timothy J. Meeks,
Administrator.
[FR Doc. E8–1504 Filed 1–29–08; 8:45 am]
BILLING CODE 6450–01–P
ENVIRONMENTAL PROTECTION
AGENCY
[EPA–HQ–OPP–2007–0179; FRL–8348–2]
Experimental Use Permit; Receipt of
Amendment Application
Environmental Protection
Agency (EPA).
ACTION: Notice.
AGENCY:
SUMMARY: This notice announces receipt
of an application 264–EUP–140 from
Bayer CropScience requesting to amend
and extend the existing experimental
use permit (EUP) for the Bacillus
thuringiensis Cry1Ab protein and the
genetic material necessary for its
production in event T303–3 and T304–
40 cotton plants. The Agency has
determined that the application may be
of regional and national significance.
Therefore, in accordance with 40 CFR
172.11(a), the Agency is soliciting
comments on this application.
DATES: Comments must be received on
or before February 29, 2008.
ADDRESSES: Submit your comments,
identified by docket identification (ID)
number EPA–HQ–OPP–2007–0179, 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.
E:\FR\FM\30JAN1.SGM
30JAN1
mstockstill on PROD1PC66 with NOTICES
5562
Federal Register / Vol. 73, No. 20 / Wednesday, January 30, 2008 / Notices
• Delivery: OPP Regulatory Public
Docket (7502P), Environmental
Protection Agency, Rm. S–4400, One
Potomac Yard (South Bldg.), 2777 S.
Crystal Dr., 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 Facility telephone number is
(703) 305–5805.
Instructions: Direct your comments to
docket ID number EPA–HQ–OPP–2007–
0179. 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 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
website 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
VerDate Aug<31>2005
18:49 Jan 29, 2008
Jkt 214001
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 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.
FOR FURTHER INFORMATION CONTACT:
Denise Greenway, Biopesticides and
Pollution Prevention Division (7511P),
Office of Pesticide Programs,
Environmental Protection Agency, 1200
Pennsylvania Ave., NW., Washington,
DC 20460–0001; telephone number:
(703) 308–8263; e-mail address:
greenway.denise@epa.gov.
SUPPLEMENTARY INFORMATION:
I. General Information
A. Does this Action Apply to Me?
This action is directed to the public
in general. This action may, however, be
of interest to those persons who are
interested in agricultural biotechnology
or may be required to conduct testing of
pesticidal substances under the Federal
Food, Drug, and Cosmetic Act (FFDCA)
or the Federal Insecticide, Fungicide,
and Rodenticide Act (FIFRA). Since
other entities may also be interested, the
Agency has not attempted to describe all
the specific entities that may be affected
by this action. If you have any questions
regarding the applicability of this action
to a particular entity, consult the 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.
PO 00000
Frm 00069
Fmt 4703
Sfmt 4703
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
Bayer CropScience has requested an
amendment and extension of EUP 264–
EUP–140, which was first granted by
EPA on February 7, 2006 and published
in the Federal Register on July 19, 2006
(71 FR 41020) (FRL–8060–6). On March
8, 2007 this EUP was amended and
published in the Federal Register on
June 20, 2007 (72 FR 34009) (FRL–
8133–5). Under the existing EUP,
plantings are permitted through May 1,
2008. Bayer CropScience is now
proposing to extend the experimental
program until January 31, 2009 and to
amend it by conducting testing with up
to 0.018 pounds of Cry1Ab protein and
the genetic material necessary for its
production in events T303–3 and T304–
40 on 88.5 acres (out of 297 total acres)
planted to Cry1Ab-containing cotton.
The Cry1Ab protein is effective in
controlling lepidopteran larvae such as
bollworm (Helicoverpa zea) and tobacco
budworm (Heliothis virescens), which
are common pests of cotton. The
proposed program will be carried out in
the States of Arizona, California,
Georgia, Louisiana, Mississippi, North
Carolina, South Carolina, Texas, and
Puerto Rico. The proposed experimental
program includes insect efficacy trials,
and the evaluation of herbicide efficacy,
agronomic performance, and breeding
lines. Also proposed is the production
of seed blocks to evaluate seed
production, dissemination, and
E:\FR\FM\30JAN1.SGM
30JAN1
Federal Register / Vol. 73, No. 20 / Wednesday, January 30, 2008 / Notices
dormancy, and for harvest for future
experimental field trial plantings.
Washington, DC 20460, or
eargle.frances@epa.gov.
III. What Action is the Agency Taking?
Dated: January 20, 2008
Christopher P. Bliley,
Associate Administrator for Congressional
and Intergovernmental Relations.
[FR Doc. 08–402 Filed 1–29–08; 8:45 am]
Following the review of the Bayer
CropScience application and any
comments and data received in response
to this notice, EPA will decide whether
to issue or deny the EUP amendment/
extension request for this EUP program,
and if issued, the conditions under
which it is to be conducted. Any
amendment/extension of this EUP will
be announced in the Federal Register.
IV. What is the Agency’s Authority for
Taking this Action?
BILLING CODE 6560–60–M
ENVIRONMENTAL PROTECTION
AGENCY
[FRL–8522–8]
The specific legal authority for EPA to
take this action is under FIFRA section
5.
Notice of Public Workshop To Discuss
Management of Underground Injection
of Carbon Dioxide for Geologic
Sequestration Under the Safe Drinking
Water Act
List of Subjects
AGENCY:
Environmental Protection
Agency.
ACTION: Notice.
Environmental protection,
Experimental use permits.
Dated: January 17, 2008.
W. Michael McDavit,
Acting Director, Biopesticides and Pollution
Prevention Division, Office of Pesticide
Programs.
[FR Doc. E8–1412 Filed 1–29–08; 8:45 am]
BILLING CODE 6560–50–S
ENVIRONMENTAL PROTECTION
AGENCY
[FRL–8522–7]
Local Government Advisory
Committee Notice of Charter Renewal
Environmental Protection
Agency (EPA).
ACTION: Notice of Charter Renewal.
mstockstill on PROD1PC66 with NOTICES
AGENCY:
The Charter for the Environmental
Protection Agency’s Local Government
Advisory Committee (LGAC) will be
renewed for an additional two-year
period, as a necessary committee which
is in the public interest, in accordance
with the provisions of the Federal
Advisory Committee Act (FACA), 5
U.S.C. App. 2 Section 9(c). The purpose
of the LGAC is to provide advice and
recommendations to EPA’s
Administrator on ways to improve its
partnership with Local Governments
and provide more efficient and effective
environmental protection.
It is determined that the LGAC is in
the public interest in connection with
the performance of duties imposed on
the Agency by law.
Inquiries may be directed to Frances
Eargle, Designated Federal Officer,
LGAC, U.S. EPA (mail code 1301A),
1200 Pennsylvania Avenue, NW.,
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18:49 Jan 29, 2008
Jkt 214001
SUMMARY: The Environmental Protection
Agency (EPA) is holding a second
public workshop to discuss the
development of proposed regulations for
the underground injection of carbon
dioxide (CO2) for geologic sequestration
under the Safe Drinking Water Act
(SDWA). The SDWA requires EPA to
protect underground sources of drinking
water from contamination due to
underground injection activities. The
Underground Injection Control Program
works with States and Tribes to oversee
underground injection activities and
prevent endangerment of drinking water
sources. This public workshop will
provide an opportunity for dialogue
with representatives from industry,
government, public interest groups, and
the general public on geologic
sequestration of carbon dioxide.
DATES: This public workshop will be
held from 1 p.m. to 5:30 p.m., Eastern
time, on Tuesday, February 26, 2008,
and from 8:30 a.m. to 5 p.m. on
Wednesday, February 27, 2008. To
register for this workshop, please visit
the following site: https://www.
resolv.org/calendar/view_recurring_
event.asp?CalendarID=10577. If you
experience difficulties with the
registration Web site, you may contact
Kate Zimmer at RESOLVE at
kzimmer@resolv.org. Please register by
February 18, 2008. Also note that while
this workshop is open to the public,
space is limited due to room capacity
restrictions. We encourage you to
register to ensure participation.
ADDRESSES: The meetings will be held at
the Crystal City Sheraton Hotel. The
hotel is located at 1800 Jefferson Davis
Highway in Arlington, VA, two blocks
from the Crystal City Metro Station. The
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Fmt 4703
Sfmt 4703
5563
hotel’s telephone number is (703) 486–
1111.
FOR FURTHER INFORMATION CONTACT: For
general information about these
meetings, please contact Mary Rose
(Molly) Bayer by phone at (202) 564–
1981, by e-mail at
bayer.maryrose@epa.gov, or by mail at:
U.S. Environmental Protection Agency,
Mail Code 4606M, 1200 Pennsylvania
Ave., NW., Washington DC 20460. For
information about EPA’s Underground
Injection Control Program & geologic
sequestration activities visit the
following Web site: https://www.epa.gov/
safewater/uic/wells_sequestration.html.
SUPPLEMENTARY INFORMATION: The
purpose of this workshop is to continue
to advance the dialogue between EPA
and stakeholders on geologic
sequestration of CO2 under SDWA and
to provide updates on the proposed rule
making process. This workshop will
also afford EPA an opportunity to seek
feedback from stakeholders on a set of
specific subjects identified as key areas
of concern and interest to stakeholders,
which were voiced during the first
workshop (December 2007) and other
EPA sponsored technical workshops,
held from 2005 to present. These
subjects may include, but are not
limited to public participation, long
term liability, site characterization/area
of review (AoR), monitoring, and UIC
well construction.
Special Accommodations
For information on access or services
for individuals with disabilities, please
contact Mary Rose (Molly) Bayer at
(202) 564–1981 or
bayer.maryrose@epa.gov. To request
accommodation of a disability, please
contact Mary Rose Bayer, preferably at
least 10 days prior to the meeting, to
give EPA as much time as possible to
process your request.
Dated: January 24, 2008.
Cynthia C. Dougherty, Director
Director, Office of Ground Water and Drinking
Water.
[FR Doc. 08–401 Filed 1–29–08; 8:45 am]
BILLING CODE 6560–50–M
ENVIRONMENTAL PROTECTION
AGENCY
[EPA–HQ–OPP–2007–1204; FRL–8348–4]
Notice of Filing of a Pesticide Petition
for Residues of Pesticide Chemicals in
or on Various Commodities
Environmental Protection
Agency (EPA).
ACTION: Notice.
AGENCY:
E:\FR\FM\30JAN1.SGM
30JAN1
Agencies
[Federal Register Volume 73, Number 20 (Wednesday, January 30, 2008)]
[Notices]
[Pages 5561-5563]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E8-1412]
=======================================================================
-----------------------------------------------------------------------
ENVIRONMENTAL PROTECTION AGENCY
[EPA-HQ-OPP-2007-0179; FRL-8348-2]
Experimental Use Permit; Receipt of Amendment Application
AGENCY: Environmental Protection Agency (EPA).
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: This notice announces receipt of an application 264-EUP-140
from Bayer CropScience requesting to amend and extend the existing
experimental use permit (EUP) for the Bacillus thuringiensis Cry1Ab
protein and the genetic material necessary for its production in event
T303-3 and T304-40 cotton plants. The Agency has determined that the
application may be of regional and national significance. Therefore, in
accordance with 40 CFR 172.11(a), the Agency is soliciting comments on
this application.
DATES: Comments must be received on or before February 29, 2008.
ADDRESSES: Submit your comments, identified by docket identification
(ID) number EPA-HQ-OPP-2007-0179, 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.
[[Page 5562]]
Delivery: OPP Regulatory Public Docket (7502P),
Environmental Protection Agency, Rm. S-4400, One Potomac Yard (South
Bldg.), 2777 S. Crystal Dr., 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 Facility telephone number is (703) 305-5805.
Instructions: Direct your comments to docket ID number EPA-HQ-OPP-
2007-0179. 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 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
website 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 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.
FOR FURTHER INFORMATION CONTACT: Denise Greenway, Biopesticides and
Pollution Prevention Division (7511P), Office of Pesticide Programs,
Environmental Protection Agency, 1200 Pennsylvania Ave., NW.,
Washington, DC 20460-0001; telephone number: (703) 308-8263; e-mail
address: greenway.denise@epa.gov.
SUPPLEMENTARY INFORMATION:
I. General Information
A. Does this Action Apply to Me?
This action is directed to the public in general. This action may,
however, be of interest to those persons who are interested in
agricultural biotechnology or may be required to conduct testing of
pesticidal substances under the Federal Food, Drug, and Cosmetic Act
(FFDCA) or the Federal Insecticide, Fungicide, and Rodenticide Act
(FIFRA). Since other entities may also be interested, the Agency has
not attempted to describe all the specific entities that may be
affected by this action. If you have any questions regarding the
applicability of this action to a particular entity, consult the 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
Bayer CropScience has requested an amendment and extension of EUP
264-EUP-140, which was first granted by EPA on February 7, 2006 and
published in the Federal Register on July 19, 2006 (71 FR 41020) (FRL-
8060-6). On March 8, 2007 this EUP was amended and published in the
Federal Register on June 20, 2007 (72 FR 34009) (FRL-8133-5). Under the
existing EUP, plantings are permitted through May 1, 2008. Bayer
CropScience is now proposing to extend the experimental program until
January 31, 2009 and to amend it by conducting testing with up to 0.018
pounds of Cry1Ab protein and the genetic material necessary for its
production in events T303-3 and T304-40 on 88.5 acres (out of 297 total
acres) planted to Cry1Ab-containing cotton. The Cry1Ab protein is
effective in controlling lepidopteran larvae such as bollworm
(Helicoverpa zea) and tobacco budworm (Heliothis virescens), which are
common pests of cotton. The proposed program will be carried out in the
States of Arizona, California, Georgia, Louisiana, Mississippi, North
Carolina, South Carolina, Texas, and Puerto Rico. The proposed
experimental program includes insect efficacy trials, and the
evaluation of herbicide efficacy, agronomic performance, and breeding
lines. Also proposed is the production of seed blocks to evaluate seed
production, dissemination, and
[[Page 5563]]
dormancy, and for harvest for future experimental field trial
plantings.
III. What Action is the Agency Taking?
Following the review of the Bayer CropScience application and any
comments and data received in response to this notice, EPA will decide
whether to issue or deny the EUP amendment/extension request for this
EUP program, and if issued, the conditions under which it is to be
conducted. Any amendment/extension of this EUP will be announced in the
Federal Register.
IV. What is the Agency's Authority for Taking this Action?
The specific legal authority for EPA to take this action is under
FIFRA section 5.
List of Subjects
Environmental protection, Experimental use permits.
Dated: January 17, 2008.
W. Michael McDavit,
Acting Director, Biopesticides and Pollution Prevention Division,
Office of Pesticide Programs.
[FR Doc. E8-1412 Filed 1-29-08; 8:45 am]
BILLING CODE 6560-50-S