Experimental Use Permit; Receipt of Application; Amendment, 71907-71908 [E7-24601]
Download as PDF
Federal Register / Vol. 72, No. 243 / Wednesday, December 19, 2007 / Notices
concerns associated with a particular
chemical.
List of Subjects
Environmental protection, Pesticides
and pests.
Dated: December 11, 2007.
´
Kathryn Bouve,
Acting Director, Information Technology and
Resource Management Division, Office of
Pesticide Programs.
[FR Doc. E7–24604 Filed 12–18–07; 8:45 am]
BILLING CODE 6560–50–S
ENVIRONMENTAL PROTECTION
AGENCY
[EPA–HQ–OPP–2007–1047; FRL–8343–4]
Experimental Use Permit; Receipt of
Application; Amendment
Environmental Protection
Agency (EPA).
ACTION: Notice.
mstockstill on PROD1PC66 with NOTICES
AGENCY:
SUMMARY: This notice announces receipt
of an application 524–EUP–97 from
Monsanto Company requesting an
amendment to the experimental use
permit (EUP) for Bacillus thuringiensis
Cry1A.105 protein and the genetic
material necessary for its production
(vector PV–ZMIR245) in event MON
89034 corn, Bacillus thuringiensis
Cry2Ab2 protein and the genetic
material necessary for its production
(vector PV–ZMIR245) in event MON
89034 corn, and Bacillus thuringiensis
Cry3Bb1 protein and the genetic
material (vector PV–ZMIR39) necessary
for its production in event MON 88017
corn. 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 January 18, 2008.
ADDRESSES: Submit your comments,
identified by docket identification (ID)
number EPA–HQ–OPP–2007–1047, 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 Bldg.), 2777 S.
Crystal Dr., Arlington, VA. Deliveries
are only accepted during the Docket’s
VerDate Aug<31>2005
21:40 Dec 18, 2007
Jkt 214001
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–
1047. 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
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
PO 00000
Frm 00037
Fmt 4703
Sfmt 4703
71907
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:
Susanne Cerrelli, Biopesticides and
Pollution Prevention Division (7511P),
Office of Pesticide Programs,
Environmental Protection Agency, 1200
Pennsylvania Ave., NW., Washington,
DC 20460–0001; telephone number:
(703) 308–8077; e-mail address:
cerrelli.susanne@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 or
may be required to conduct testing of
chemical 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).
E:\FR\FM\19DEN1.SGM
19DEN1
71908
Federal Register / Vol. 72, No. 243 / Wednesday, December 19, 2007 / Notices
mstockstill on PROD1PC66 with NOTICES
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
On June 29, 2006, EPA approved
Monsanto’s application for an EUP for
the testing of MON 89034 x MON 88017
combined insecticidal trait corn as well
as MON 89034 and MON 88017
individually (524–EUP–97). This permit
allows planting through June 20, 2008.
MON 89034 contains the lepidopteran
protecting Bacillus thuringiensis
Cry1A.105 protein and the genetic
material necessary (vector PV–
ZMIR245) for its production in MON
89034 corn and Bacillus thuringiensis
Cry2Ab2 protein and the genetic
material necessary (vector PV–
ZMIR245) for its production in MON
89034 corn. MON 88017 contains the
corn rootworm protecting Bacillus
thuringiensis Cry3Bb1 protein and the
genetic material necessary (vector PV–
ZMIR39) for its production in MON
88017 corn.
Monsanto proposes amending the
EUP to allow the treatment of 11,952
acres in total. This includes a maximum
of 4,421 acres for MON 89034 x MON
88017, 3,687 acres of MON 89034, 1,742
acres of MON 88017, 415 acres of corn
containing registered plant-incorporated
protectants (PIPS) and 1,687 acres of
non-PIP and border rows. The proposed
period of use of this amended EUP is
February 15, 2008–June 15, 2009.
Eight trial protocols are proposed to
be conducted including:
• Breeding and observation nursery.
• Inbred seed increase and sample
hybrid production.
• Line per se hybrid yield and
herbicide tolerance trials.
• Insect efficacy trials.
• Product characterization and
performance trials.
VerDate Aug<31>2005
21:40 Dec 18, 2007
Jkt 214001
• Insect resistance management trials.
• Benefit trials.
• Seed treatment trials.
States and Commonwealth involved
include: Alabama, Arizona, California,
Colorado, Delaware, Florida, Georgia,
Hawaii, Idaho, Illinois, Indiana, Iowa,
Kansas, Kentucky, Louisiana, Maryland,
Massachusetts, Michigan, Minnesota,
Mississippi, Missouri, Nebraska, New
Jersey, New Mexico, New York, North
Carolina, Ohio, Oklahoma, Oregon,
Pennsylvania, Puerto Rico, South
Carolina, South Dakota, Tennessee,
Texas, Washington, and Wisconsin.
III. What Action is the Agency Taking?
Following the review of the Monsanto
Company application and any
comments and data received in response
to this notice, EPA will decide whether
to issue or deny the EUP request for this
EUP program, and if issued, the
conditions under which it is to be
conducted. Any issuance of an EUP will
be announced in the Federal Register.
IV. What is the Agency’s Authority for
Taking this Action?
The Agency’s authority for taking this
action is under FIFRA section 5.
List of Subjects
Environmental protection,
Experimental use permits.
Dated: December 10, 2007.
Janet L. Andersen,
Director, Biopesticides and Pollution
Prevention Division, Office of Pesticide
Programs.
[FR Doc. E7–24601 Filed 12–18–07; 8:45 am]
BILLING CODE 6560–50–S
OFFICE OF SCIENCE AND
TECHNOLOGY POLICY
Meeting of the President’s Council of
Advisors on Science and Technology
ACTION:
Notice of meeting.
SUMMARY: This notice sets forth the
schedule and summary agenda for a
meeting of the President’s Council of
Advisors on Science and Technology
(PCAST), and describes the functions of
the Council. Notice of this meeting is
required under the Federal Advisory
Committee Act (FACA).
Dates and Place: January 8, 2008,
Washington, DC. The meeting will be
held in Room 100 at the Keck Center of
the National Academies at 500 5th St.
NW., Washington DC.
Type of Meeting: Open. Further
details on the meeting agenda will be
posted on the PCAST Web site at:
https://www.ostp.gov/PCAST/pcast.html.
PO 00000
Frm 00038
Fmt 4703
Sfmt 4703
Proposed Schedule and Agenda: The
President’s Council of Advisors on
Science and Technology (PCAST) is
scheduled to meet in open session on
Tuesday January 8, 2008, at
approximately 9 a.m. The co-chairs of
the PCAST subcommittee on
nanotechnology are tentatively
scheduled to lead a discussion on the
findings of the PCAST review of the
National Nanotechnology Initiative
(NNI). The PCAST also is tentatively
scheduled to convene two panels. The
first panel will address approaches and
barriers to research partnerships among
universities and the private sector. The
second panel will address policy issues
associated with realizing the benefits of
personalized medicine. This session
will end at approximately 4 p.m.
Additional information and the final
agenda will be posted at the PCAST
Web site at: https://www.ostp.gov/
PCAST/pcast.html.
Public Comments: There will be time
allocated for the public to speak on the
above agenda items. This public
comment time is designed for
substantive commentary on PCAST’s
work topics, not for business marketing
purposes. Please submit a request for
the opportunity to make a public
comment five (5) days in advance of the
meeting. The time for public comments
will be limited to no more than 5
minutes per person. Written comments
are also welcome at any time following
the meeting. Please notify Dr. Celia
Merzbacher, PCAST Executive Director,
at (202) 456–7116, or fax your request/
comments to (202) 456–6021.
FOR FURTHER INFORMATION CONTACT:
Information regarding agenda, time, and
location is available at the PCAST Web
site at: https://www.ostp.gov/PCAST/
pcast.html. Questions about the meeting
should be directed to PCAST Executive
Director Dr. Celia Merzbacher at (202)
456–7116 prior to 3 p.m. on Friday,
January 4, 2008. Please note that public
seating for this meeting is limited and
is available on a first-come, first-served
basis.
SUPPLEMENTARY INFORMATION: The
President’s Council of Advisors on
Science and Technology was
established by Executive Order 13226,
on September 30, 2001. The purpose of
PCAST is to advise the President on
matters of science and technology
policy, and to assist the President’s
National Science and Technology
Council in securing private sector
participation in its activities. The
Council members are distinguished
individuals appointed by the President
from non-Federal sectors. The PCAST is
co-chaired by Dr. John H. Marburger, III,
E:\FR\FM\19DEN1.SGM
19DEN1
Agencies
[Federal Register Volume 72, Number 243 (Wednesday, December 19, 2007)]
[Notices]
[Pages 71907-71908]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E7-24601]
-----------------------------------------------------------------------
ENVIRONMENTAL PROTECTION AGENCY
[EPA-HQ-OPP-2007-1047; FRL-8343-4]
Experimental Use Permit; Receipt of Application; Amendment
AGENCY: Environmental Protection Agency (EPA).
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: This notice announces receipt of an application 524-EUP-97
from Monsanto Company requesting an amendment to the experimental use
permit (EUP) for Bacillus thuringiensis Cry1A.105 protein and the
genetic material necessary for its production (vector PV-ZMIR245) in
event MON 89034 corn, Bacillus thuringiensis Cry2Ab2 protein and the
genetic material necessary for its production (vector PV-ZMIR245) in
event MON 89034 corn, and Bacillus thuringiensis Cry3Bb1 protein and
the genetic material (vector PV-ZMIR39) necessary for its production in
event MON 88017 corn. 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 January 18, 2008.
ADDRESSES: Submit your comments, identified by docket identification
(ID) number EPA-HQ-OPP-2007-1047, 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
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-
2007-1047. 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: Susanne Cerrelli, Biopesticides and
Pollution Prevention Division (7511P), Office of Pesticide Programs,
Environmental Protection Agency, 1200 Pennsylvania Ave., NW.,
Washington, DC 20460-0001; telephone number: (703) 308-8077; e-mail
address: cerrelli.susanne@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 or may be required to
conduct testing of chemical 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).
[[Page 71908]]
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
On June 29, 2006, EPA approved Monsanto's application for an EUP
for the testing of MON 89034 x MON 88017 combined insecticidal trait
corn as well as MON 89034 and MON 88017 individually (524-EUP-97). This
permit allows planting through June 20, 2008. MON 89034 contains the
lepidopteran protecting Bacillus thuringiensis Cry1A.105 protein and
the genetic material necessary (vector PV-ZMIR245) for its production
in MON 89034 corn and Bacillus thuringiensis Cry2Ab2 protein and the
genetic material necessary (vector PV-ZMIR245) for its production in
MON 89034 corn. MON 88017 contains the corn rootworm protecting
Bacillus thuringiensis Cry3Bb1 protein and the genetic material
necessary (vector PV-ZMIR39) for its production in MON 88017 corn.
Monsanto proposes amending the EUP to allow the treatment of 11,952
acres in total. This includes a maximum of 4,421 acres for MON 89034 x
MON 88017, 3,687 acres of MON 89034, 1,742 acres of MON 88017, 415
acres of corn containing registered plant-incorporated protectants
(PIPS) and 1,687 acres of non-PIP and border rows. The proposed period
of use of this amended EUP is February 15, 2008-June 15, 2009.
Eight trial protocols are proposed to be conducted including:
Breeding and observation nursery.
Inbred seed increase and sample hybrid production.
Line per se hybrid yield and herbicide tolerance trials.
Insect efficacy trials.
Product characterization and performance trials.
Insect resistance management trials.
Benefit trials.
Seed treatment trials.
States and Commonwealth involved include: Alabama, Arizona,
California, Colorado, Delaware, Florida, Georgia, Hawaii, Idaho,
Illinois, Indiana, Iowa, Kansas, Kentucky, Louisiana, Maryland,
Massachusetts, Michigan, Minnesota, Mississippi, Missouri, Nebraska,
New Jersey, New Mexico, New York, North Carolina, Ohio, Oklahoma,
Oregon, Pennsylvania, Puerto Rico, South Carolina, South Dakota,
Tennessee, Texas, Washington, and Wisconsin.
III. What Action is the Agency Taking?
Following the review of the Monsanto Company application and any
comments and data received in response to this notice, EPA will decide
whether to issue or deny the EUP request for this EUP program, and if
issued, the conditions under which it is to be conducted. Any issuance
of an EUP will be announced in the Federal Register.
IV. What is the Agency's Authority for Taking this Action?
The Agency's authority for taking this action is under FIFRA
section 5.
List of Subjects
Environmental protection, Experimental use permits.
Dated: December 10, 2007.
Janet L. Andersen,
Director, Biopesticides and Pollution Prevention Division, Office of
Pesticide Programs.
[FR Doc. E7-24601 Filed 12-18-07; 8:45 am]
BILLING CODE 6560-50-S