FIFRA Scientific Advisory Panel; Notice of Public Meeting, 21125-21128 [E8-8399]
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[FR Doc. E8–8397 Filed 4–17–08; 8:45 am]
BILLING CODE 6560–50–P
ENVIRONMENTAL PROTECTION
AGENCY
[EPA–HQ–OPP–2008–0274; FRL–8360–8]
FIFRA Scientific Advisory Panel;
Notice of Public Meeting
Environmental Protection
Agency (EPA).
ACTION: Notice.
AGENCY:
There will be a 4 –day
meeting of the Federal Insecticide,
Fungicide, and Rodenticide Act
Scientific Advisory Panel (FIFRA SAP)
to consider and review The Agency’s
Evaluation of the Toxicity Profile of
Chlorpyrifos.
SUMMARY:
The meeting will be held on July
15–18, 2008, from 9 a.m. to 5:30 p.m,
Eastern Time.
Comments. The Agency encourages
that written comments be submitted by
July 7, 2008 and requests for oral
comments be submitted by July 10,
2008. However, written comments and
requests to make oral comments may be
submitted until the date of the meeting.
Anyone submitting written comments
after July 7, 2008 should contact the
Designated Federal Official (DFO) listed
under FOR FURTHER INFORMATION
CONTACT. For additional instructions,
see Unit I.C. of the SUPPLEMENTARY
INFORMATION.
DATES:
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Nominations. Nominations of
candidates to serve as ad hoc members
of the FIFRA SAP for this meeting
should be provided on or before May 2,
2008.
Special accommodations. For
information on access or services for
individuals with disabilities, and to
request accommodation of a disability,
please contact the DFO listed under FOR
FURTHER INFORMATION CONTACT at least
10 days prior to the meeting to give EPA
as much time as possible to process
your request.
ADDRESSES: The meeting will be held at
Environmental Protection Agency
Conference Center, Lobby Level, One
Potomac Yard (South Bldg.), 2777
Crystal Dr., Arlington, VA 22202.
Comments. Submit your comments,
identified by docket identification (ID)
number EPA–HQ–OPP–2008–0274, 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–2008–
0274. If your comments contain any
information that you consider to be CBI
or otherwise protected, please contact
the DFO listed under FOR FURTHER
INFORMATION CONTACT to obtain special
instructions before submitting your
comments. 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
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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 a 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 a docket 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 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.
Nominations, requests to present oral
comments, and requests for special
accommodations. Submit nominations
to serve as an ad hoc member of the
FIFRA SAP, requests for special seating
accommodations, or requests to present
oral comments to the DFO listed under
FOR FURTHER INFORMATION CONTACT.
FOR FURTHER INFORMATION CONTACT:
Sharlene R. Matten, DFO, Office of
Science Coordination and Policy
(7201M), Environmental Protection
Agency, 1200 Pennsylvania Ave., NW.,
Washington, DC 20460–0001; telephone
number: (202) 564–0130; fax number:
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(202) 564–8382; e-mail addresses:
matten.sharlene@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 persons who are or may be
required to conduct testing of chemical
substances under the Federal Food,
Drug, and Cosmetic Act (FFDCA),
FIFRA, and the Food Quality Protection
Act of 1996 (FQPA). 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 DFO
listed under FOR FURTHER INFORMATION
CONTACT.
B. What Should I Consider as I Prepare
My Comments for EPA?
When submitting comments,
remember to:
1. Identify the document by docket ID
number and other identifying
information (subject heading, Federal
Register date and page number).
2. 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.
3. Explain why you agree or disagree;
suggest alternatives and substitute
language for your requested changes.
4. Describe any assumptions and
provide any technical information and/
or data that you used.
5. If you estimate potential costs or
burdens, explain how you arrived at
your estimate in sufficient detail to
allow for it to be reproduced.
6. Provide specific examples to
illustrate your concerns and suggest
alternatives.
7. Explain your views as clearly as
possible, avoiding the use of profanity
or personal threats.
8. Make sure to submit your
comments by the comment period
deadline identified.
C. How May I Participate in this
Meeting?
You may participate in this meeting
by following the instructions in this
unit. To ensure proper receipt by EPA,
it is imperative that you identify docket
ID number EPA–HQ–OPP–2008–0274 in
the subject line on the first page of your
request.
1. Written comments. The Agency
encourages that written comments be
submitted, using the instructions in
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ADDRESSES,
no later than July 7, 2008, to
provide FIFRA SAP the time necessary
to consider and review the written
comments. However, written comments
are accepted until the date of the
meeting. Persons wishing to submit
written comments at the meeting should
contact the DFO listed under FOR
FURTHER INFORMATION CONTACT and
submit 30 copies. Anyone submitting
written comments after July 7, 2008
should contact the DFO listed under FOR
FURTHER INFORMATION CONTACT. There is
no limit on the extent of written
comments for consideration by FIFRA
SAP.
2. Oral comments. The Agency
encourages that each individual or
group wishing to make brief oral
comments to FIFRA SAP submit their
request to the DFO listed under FOR
FURTHER INFORMATION CONTACT no later
than July 10, 2008, in order to be
included on the meeting agenda.
Requests to present oral comments will
be accepted until the date of the meeting
and, to the extent that time permits, the
Chair of the FIFRA SAP may permit the
presentation of oral comments at the
meeting by interested persons who have
not previously requested time. The
request should identify the name of the
individual making the presentation, the
organization (if any) the individual will
represent, and any requirements for
audiovisual equipment (e.g., overhead
projector, 35 mm projector, chalkboard).
Oral comments before FIFRA SAP are
limited to approximately 5 minutes
unless prior arrangements have been
made. In addition, each speaker should
bring 30 copies of his or her comments
and presentation slides for distribution
to the FIFRA SAP at the meeting.
3. Seating at the meeting. Seating at
the meeting will be on a first-come
basis.
4. Request for nominations to serve as
ad hoc members of the FIFRA SAP for
this meeting. As part of a broader
process for developing a pool of
candidates for each meeting, the FIFRA
SAP staff routinely solicits the
stakeholder community for nominations
of prospective candidates for service as
ad hoc members of the FIFRA SAP. Any
interested person or organization may
nominate qualified individuals to be
considered as prospective candidates for
a specific meeting. Individuals
nominated for this meeting should have
expertise in one or more of the
following areas:
i. Organophosphate pesticides.
ii. Acetylcholinesterase inhibition.
iii. Chlorpyrifos metabolism including
paraoxonase 1 (PON 1) expression and
activity.
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iv. Cholinergic and non-cholinergic
modes/mechanisms of toxicity.
v. Developmental neurotoxicity.
vi. Physiologically-based
pharmacokinetic modeling.
vii. Interpretation of metabolite data
from human samples.
viii. Mode of action framework.
ix Human relevance framework.
x. Human health risk assessment.
xi. Epidemiology.
xii. IPSC WHO Guidance on Chemical
Specific Adjustment Factors.
Nominees should be scientists who
have sufficient
professionalqualifications, including
training and experience, to be capable of
providing expert comments on the
scientific issues for this meeting.
Nominees should be identified by name,
occupation, position, address, and
telephone number. Nominations should
be provided to the DFO listed under FOR
FURTHER INFORMATION CONTACT on or
before May 2, 2008. The Agency will
consider all nominations of prospective
candidates for this meeting that are
received on or before this date.
However, final selection of ad hoc
members for this meeting is a
discretionary function of the Agency.
The selection of scientists to serve on
the FIFRA SAP is based on the function
of the panel and the expertise needed to
address the Agency’s charge to the
panel. No interested scientists shall be
ineligible to serve by reason of their
membership on any other advisory
committee to a Federal department or
agency or their employment by a
Federal department or agency except the
EPA. Other factors considered during
the selection process include
availability of the potential panel
member to fully participate in the
panel’s reviews, absence of any conflicts
of interest or appearance of lack of
impartiality, independence with respect
to the matters under review, and lack of
bias. Although, financial conflicts of
interest, the appearance of lack of
impartiality, lack of independence, and
bias may result in disqualification, the
absence of such concerns does not
assure that a candidate will be selected
to serve on the FIFRA SAP. Numerous
qualified candidates are identified for
each panel. Therefore, selection
decisions involve carefully weighing a
number of factors including the
candidates’ areas of expertise and
professional qualifications and
achieving an overall balance of different
scientific perspectives on the panel.
In order to have the collective breadth
of experience needed to address the
Agency’s charge for this meeting, the
Agency anticipates selecting
approximately 10 to 15 ad hoc
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21127
scientists. FIFRA SAP members are
subject to the provisions of 5 CFR part
2634, Executive Branch Financial
Disclosure, as supplemented by the EPA
in 5 CFR part 6401. In anticipation of
this requirement, prospective
candidates for service on the FIFRA
SAP will be asked to submit
confidential financial information
which shall fully disclose, among other
financial interests, the candidate’s
employment, stocks and bonds, and
where applicable, sources of research
support. The EPA will evaluate the
candidates financial disclosure form to
assess whether there are financial
conflicts of interest, appearance of a
lack of impartiality or any prior
involvement with the development of
the documents under consideration
(including previous scientific peer
review) before the candidate is
considered further for service on the
FIFRA SAP. Those who are selected
from the pool of prospective candidates
will be asked to attend the public
meetings and to participate in the
discussion of key issues and
assumptions at these meetings. In
addition, they will be asked to review
and to help finalize the meeting
minutes. The list of FIFRA SAP
members participating at this meeting
will be posted on the FIFRA SAP
website at https://epa.gov/scipoly/sap or
may be obtained from the OPP
Regulatory Public Docket at https://
www.regulations.gov.
II. Background
A. Purpose of the FIFRA SAP
The FIFRA SAP serves as the primary
scientific peer review mechanism of
EPA’s Office of Prevention, Pesticides
and Toxic Substances (OPPTS) and is
structured to provide scientific advice,
information and recommendations to
the EPA Administrator on pesticides
and pesticide-related issues as to the
impact of regulatory actions on health
and the environment. The FIFRA SAP is
a Federal advisory committee
established in 1975 under FIFRA that
operates in accordance with
requirements of the Federal Advisory
Committee Act. The FIFRA SAP is
composed of a permanent panel
consisting of seven members who are
appointed by the EPA Administrator
from nominees provided by the National
Institutes of Health and the National
Science Foundation. FIFRA, as
amended by FQPA, established a
Science Review Board consisting of at
least 60 scientists who are available to
the Scientific Advisory Panel on an ad
hoc basis to assist in reviews conducted
by the Scientific Advisory Panel. As a
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peer review mechanism, the FIFRA SAP
provides comments, evaluations and
recommendations to improve the
effectiveness and quality of analyses
made by Agency scientists. Members of
the FIFRA SAP are scientists who have
sufficient professional qualifications,
including training and experience, to
provide expert advice and
recommendation to the Agency.
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B. Public Meeting
In the last decade, there has been a
substantial amount of research on the
human health effects of chlorpyrifos.
The Agency is currently updating the
hazard identification and hazard
characterization for chlorpyrifos, in
part, by evaluating aspects of this
research. The Agency is particularly
focusing on studies that evaluate the
effects of chlorpyrifos on infants and
children from in utero and/or post-natal
exposures and on studies that evaluate
population variability with respect to
response to chlorpyrifos. This review
will encompass selected human
epidemiological data, in vivo data in
laboratory animals and in vitro studies.
The Agency will be seeking comments
from the SAP on the following areas:
1. Interpretation of recent
epidemiological studies associating in
utero and/or post-natal chlorpyrifos
exposure with health outcomes;
2. Aspects of chlorpyrifos metabolism,
such as differences in paraoxonase 1
(PON 1) expression and activity, which
affects population variability with
respect to the effects of chlorpyrifos and
its oxon metabolite; and
3. Cholinergic and non-cholinergic
modes/mechanisms of toxicity which
are relevant to evaluating hazard and
risk to infants and children.
As part of this review, the Agency is
evaluating the relevance of animal
studies conducted by different routes of
administration (e.g., gavage or
subcutaneous injection) for conducting
human health risk assessment to
different age groups and by different
exposure pathways.
C. FIFRA SAP Documents and Meeting
Minutes
EPA’s background paper, related
supporting materials, charge/questions
to the FIFRA SAP, FIFRA SAP
composition (i.e., members and ad hoc
members for this meeting), and the
meeting agenda will be available by late
June 2008. In addition, the Agency may
provide additional background
documents as the materials become
available. You may obtain electronic
copies of these documents, and certain
other related documents that might be
available electronically, at https://
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www.regulations.gov and the FIFRA
SAP homepage at https://www.epa.gov/
scipoly/sap.
The FIFRA SAP will prepare meeting
minutes summarizing its
recommendations to the Agency
approximately 90 days after the
meeting. The meeting minutes will be
posted on the FIFRA SAP website or
may be obtained from the OPP
Regulatory Public Docket at https://
www.regulations.gov.
List of Subjects
Environmental protection, Pesticides
and pests.
Dated: April 10, 2008.
Elizabeth A. Resek,
Acting Director, Office of Science
Coordination and Policy.
[FR Doc. E8–8399 Filed 4–17–08; 8:45 a.m.]
BILLING CODE 6560–50–S
ENVIRONMENTAL PROTECTION
AGENCY
[FRL–8555–7]
Science Advisory Board Staff Office;
Notification of a Meeting of the Science
Advisory Board’s Advisory Council on
Clean Air Compliance Analysis
(Council)
Environmental Protection
Agency (EPA).
ACTION: Notice.
AGENCY:
SUMMARY: The EPA Science Advisory
Board (SAB) Staff Office announces a
public face-to-face meeting of the
Advisory Council on Clean Air
Compliance Analysis (Council).
DATES: The meeting dates are Thursday,
May 8, 2008, from 8:30 a.m. to 5 p.m.
and Friday, May 9, 2008, from 8:30 a.m.
to 3 p.m. (Eastern Time).
ADDRESSES: The meeting will be held at
the SAB Conference Center at 1025 F
Street, NW., Suite 3700, Washington,
DC 20004.
FOR FURTHER INFORMATION CONTACT:
Members of the public who wish to
obtain further information about this
meeting may contact Dr. Holly
Stallworth, Designated Federal Officer
(DFO), EPA Science Advisory Board
Staff Office (1400F), U.S. Environmental
Protection Agency, 1200 Pennsylvania
Avenue, NW., Washington, DC 20460;
by telephone/voice mail: (202) 343–
9867 or at stallworth.holly@epa.gov.
General information about the SAB, as
well as any updates concerning the
meeting announced in this notice, may
be found on the SAB Web Site at:
https://www.epa.gov/sab.
SUPPLEMENTARY INFORMATION:
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Background: The Advisory Council
on Clean Air Compliance Analysis
(Council) is a Federal advisory
committee chartered under the Federal
Advisory Committee Act (FACA), as
amended, 5 U.S.C., App. The Council is
charged with providing advice,
information and recommendations to
the Agency on the economic issues
associated with programs implemented
under the Clean Air Act and its
Amendments. Pursuant to a requirement
under Section 812 of the 1990 Clean Air
Act Amendments, EPA conducts
periodic studies to assess the benefits
and the costs of the Clean Air Act. The
Council has been the chief reviewing
body for these studies and has issued
advice on a retrospective study issued
in 1997, a prospective study issued in
1999 and since 2001, analytic blueprints
for a second prospective study on the
costs and benefits of clean air programs
covering the years 1990–2020.
On May 9, 2008, the Council will
review a case study entitled ‘‘Section
812 Prospective Study of the Benefits
and Costs of the Clean Air Act: Air
Toxics Case Study—Health Benefits of
Benzene Reductions in Houston, 1990–
2020.’’ This case study presents a
methodology for assessing the benefits
of reducing benzene levels in the
Houston, Texas, area over 30 years.
EPA’s Office of Air and Radiation (OAR)
conducted this case study (posted at
https://www.epa.gov/air/sect812/
prospective2.html#mar08/) as part of
the second prospective study on the
costs and benefits of the Clean Air Act
programs being developed by EPA’s
Office of Air and Radiation (OAR).
EPA’s OAR has also requested the
Council’s advice on using results of a
recently conducted expert elicitation in
the regulatory context of a benefits
assessment conducted as part of a
regulatory impact analysis for a
regulation promulgated in 2006. To
better characterize uncertainty in the
health benefits of particulate matter
reductions, EPA’s Office of Air and
Radiation undertook an expert
elicitation study in 2005–2006 to
characterize the uncertainty in the
concentration-response function for
premature mortality related to
particulate matter, specifically PM2.5.
EPA applied the results of this study to
develop probabilistic estimates of
reductions in premature mortality as
part of its regulatory impact analysis for
the 2006 National Ambient Air Quality
Standards for Particle Pollution. The
Council’s review will focus on Chapter
5 and the Executive Summary of the
regulatory impact analysis found at
https://www.epa.gov/ttn/ecas/regdata/
RIAs/Chapter%205—Benefits.pdf. The
E:\FR\FM\18APN1.SGM
18APN1
Agencies
[Federal Register Volume 73, Number 76 (Friday, April 18, 2008)]
[Notices]
[Pages 21125-21128]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E8-8399]
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ENVIRONMENTAL PROTECTION AGENCY
[EPA-HQ-OPP-2008-0274; FRL-8360-8]
FIFRA Scientific Advisory Panel; Notice of Public Meeting
AGENCY: Environmental Protection Agency (EPA).
ACTION: Notice.
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SUMMARY: There will be a 4 -day meeting of the Federal Insecticide,
Fungicide, and Rodenticide Act Scientific Advisory Panel (FIFRA SAP) to
consider and review The Agency's Evaluation of the Toxicity Profile of
Chlorpyrifos.
DATES: The meeting will be held on July 15-18, 2008, from 9 a.m. to
5:30 p.m, Eastern Time.
Comments. The Agency encourages that written comments be submitted
by July 7, 2008 and requests for oral comments be submitted by July 10,
2008. However, written comments and requests to make oral comments may
be submitted until the date of the meeting. Anyone submitting written
comments after July 7, 2008 should contact the Designated Federal
Official (DFO) listed under FOR FURTHER INFORMATION CONTACT. For
additional instructions, see Unit I.C. of the SUPPLEMENTARY
INFORMATION.
[[Page 21126]]
Nominations. Nominations of candidates to serve as ad hoc members
of the FIFRA SAP for this meeting should be provided on or before May
2, 2008.
Special accommodations. For information on access or services for
individuals with disabilities, and to request accommodation of a
disability, please contact the DFO listed under FOR FURTHER INFORMATION
CONTACT at least 10 days prior to the meeting to give EPA as much time
as possible to process your request.
ADDRESSES: The meeting will be held at Environmental Protection Agency
Conference Center, Lobby Level, One Potomac Yard (South Bldg.), 2777
Crystal Dr., Arlington, VA 22202.
Comments. Submit your comments, identified by docket
identification (ID) number EPA-HQ-OPP-2008-0274, 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-
2008-0274. If your comments contain any information that you consider
to be CBI or otherwise protected, please contact the DFO listed under
FOR FURTHER INFORMATION CONTACT to obtain special instructions before
submitting your comments. 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 a 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 a docket 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 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.
Nominations, requests to present oral comments, and requests for
special accommodations. Submit nominations to serve as an ad hoc member
of the FIFRA SAP, requests for special seating accommodations, or
requests to present oral comments to the DFO listed under FOR FURTHER
INFORMATION CONTACT.
FOR FURTHER INFORMATION CONTACT: Sharlene R. Matten, DFO, Office of
Science Coordination and Policy (7201M), Environmental Protection
Agency, 1200 Pennsylvania Ave., NW., Washington, DC 20460-0001;
telephone number: (202) 564-0130; fax number: (202) 564-8382; e-mail
addresses: matten.sharlene@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 persons who are or may be required to
conduct testing of chemical substances under the Federal Food, Drug,
and Cosmetic Act (FFDCA), FIFRA, and the Food Quality Protection Act of
1996 (FQPA). 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 DFO
listed under FOR FURTHER INFORMATION CONTACT.
B. What Should I Consider as I Prepare My Comments for EPA?
When submitting comments, remember to:
1. Identify the document by docket ID number and other identifying
information (subject heading, Federal Register date and page number).
2. 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.
3. Explain why you agree or disagree; suggest alternatives and
substitute language for your requested changes.
4. Describe any assumptions and provide any technical information
and/or data that you used.
5. If you estimate potential costs or burdens, explain how you
arrived at your estimate in sufficient detail to allow for it to be
reproduced.
6. Provide specific examples to illustrate your concerns and
suggest alternatives.
7. Explain your views as clearly as possible, avoiding the use of
profanity or personal threats.
8. Make sure to submit your comments by the comment period deadline
identified.
C. How May I Participate in this Meeting?
You may participate in this meeting by following the instructions
in this unit. To ensure proper receipt by EPA, it is imperative that
you identify docket ID number EPA-HQ-OPP-2008-0274 in the subject line
on the first page of your request.
1. Written comments. The Agency encourages that written comments be
submitted, using the instructions in
[[Page 21127]]
ADDRESSES, no later than July 7, 2008, to provide FIFRA SAP the time
necessary to consider and review the written comments. However, written
comments are accepted until the date of the meeting. Persons wishing to
submit written comments at the meeting should contact the DFO listed
under FOR FURTHER INFORMATION CONTACT and submit 30 copies. Anyone
submitting written comments after July 7, 2008 should contact the DFO
listed under FOR FURTHER INFORMATION CONTACT. There is no limit on the
extent of written comments for consideration by FIFRA SAP.
2. Oral comments. The Agency encourages that each individual or
group wishing to make brief oral comments to FIFRA SAP submit their
request to the DFO listed under FOR FURTHER INFORMATION CONTACT no
later than July 10, 2008, in order to be included on the meeting
agenda. Requests to present oral comments will be accepted until the
date of the meeting and, to the extent that time permits, the Chair of
the FIFRA SAP may permit the presentation of oral comments at the
meeting by interested persons who have not previously requested time.
The request should identify the name of the individual making the
presentation, the organization (if any) the individual will represent,
and any requirements for audiovisual equipment (e.g., overhead
projector, 35 mm projector, chalkboard). Oral comments before FIFRA SAP
are limited to approximately 5 minutes unless prior arrangements have
been made. In addition, each speaker should bring 30 copies of his or
her comments and presentation slides for distribution to the FIFRA SAP
at the meeting.
3. Seating at the meeting. Seating at the meeting will be on a
first-come basis.
4. Request for nominations to serve as ad hoc members of the FIFRA
SAP for this meeting. As part of a broader process for developing a
pool of candidates for each meeting, the FIFRA SAP staff routinely
solicits the stakeholder community for nominations of prospective
candidates for service as ad hoc members of the FIFRA SAP. Any
interested person or organization may nominate qualified individuals to
be considered as prospective candidates for a specific meeting.
Individuals nominated for this meeting should have expertise in one or
more of the following areas:
i. Organophosphate pesticides.
ii. Acetylcholinesterase inhibition.
iii. Chlorpyrifos metabolism including paraoxonase 1 (PON 1)
expression and activity.
iv. Cholinergic and non-cholinergic modes/mechanisms of toxicity.
v. Developmental neurotoxicity.
vi. Physiologically-based pharmacokinetic modeling.
vii. Interpretation of metabolite data from human samples.
viii. Mode of action framework.
ix Human relevance framework.
x. Human health risk assessment.
xi. Epidemiology.
xii. IPSC WHO Guidance on Chemical Specific Adjustment Factors.
Nominees should be scientists who have sufficient
professionalqualifications, including training and experience, to be
capable of providing expert comments on the scientific issues for this
meeting. Nominees should be identified by name, occupation, position,
address, and telephone number. Nominations should be provided to the
DFO listed under FOR FURTHER INFORMATION CONTACT on or before May 2,
2008. The Agency will consider all nominations of prospective
candidates for this meeting that are received on or before this date.
However, final selection of ad hoc members for this meeting is a
discretionary function of the Agency.
The selection of scientists to serve on the FIFRA SAP is based on
the function of the panel and the expertise needed to address the
Agency's charge to the panel. No interested scientists shall be
ineligible to serve by reason of their membership on any other advisory
committee to a Federal department or agency or their employment by a
Federal department or agency except the EPA. Other factors considered
during the selection process include availability of the potential
panel member to fully participate in the panel's reviews, absence of
any conflicts of interest or appearance of lack of impartiality,
independence with respect to the matters under review, and lack of
bias. Although, financial conflicts of interest, the appearance of lack
of impartiality, lack of independence, and bias may result in
disqualification, the absence of such concerns does not assure that a
candidate will be selected to serve on the FIFRA SAP. Numerous
qualified candidates are identified for each panel. Therefore,
selection decisions involve carefully weighing a number of factors
including the candidates' areas of expertise and professional
qualifications and achieving an overall balance of different scientific
perspectives on the panel.
In order to have the collective breadth of experience needed to
address the Agency's charge for this meeting, the Agency anticipates
selecting approximately 10 to 15 ad hoc scientists. FIFRA SAP members
are subject to the provisions of 5 CFR part 2634, Executive Branch
Financial Disclosure, as supplemented by the EPA in 5 CFR part 6401. In
anticipation of this requirement, prospective candidates for service on
the FIFRA SAP will be asked to submit confidential financial
information which shall fully disclose, among other financial
interests, the candidate's employment, stocks and bonds, and where
applicable, sources of research support. The EPA will evaluate the
candidates financial disclosure form to assess whether there are
financial conflicts of interest, appearance of a lack of impartiality
or any prior involvement with the development of the documents under
consideration (including previous scientific peer review) before the
candidate is considered further for service on the FIFRA SAP. Those who
are selected from the pool of prospective candidates will be asked to
attend the public meetings and to participate in the discussion of key
issues and assumptions at these meetings. In addition, they will be
asked to review and to help finalize the meeting minutes. The list of
FIFRA SAP members participating at this meeting will be posted on the
FIFRA SAP website at https://epa.gov/scipoly/sap or may be obtained from
the OPP Regulatory Public Docket at https://www.regulations.gov.
II. Background
A. Purpose of the FIFRA SAP
The FIFRA SAP serves as the primary scientific peer review
mechanism of EPA's Office of Prevention, Pesticides and Toxic
Substances (OPPTS) and is structured to provide scientific advice,
information and recommendations to the EPA Administrator on pesticides
and pesticide-related issues as to the impact of regulatory actions on
health and the environment. The FIFRA SAP is a Federal advisory
committee established in 1975 under FIFRA that operates in accordance
with requirements of the Federal Advisory Committee Act. The FIFRA SAP
is composed of a permanent panel consisting of seven members who are
appointed by the EPA Administrator from nominees provided by the
National Institutes of Health and the National Science Foundation.
FIFRA, as amended by FQPA, established a Science Review Board
consisting of at least 60 scientists who are available to the
Scientific Advisory Panel on an ad hoc basis to assist in reviews
conducted by the Scientific Advisory Panel. As a
[[Page 21128]]
peer review mechanism, the FIFRA SAP provides comments, evaluations and
recommendations to improve the effectiveness and quality of analyses
made by Agency scientists. Members of the FIFRA SAP are scientists who
have sufficient professional qualifications, including training and
experience, to provide expert advice and recommendation to the Agency.
B. Public Meeting
In the last decade, there has been a substantial amount of research
on the human health effects of chlorpyrifos. The Agency is currently
updating the hazard identification and hazard characterization for
chlorpyrifos, in part, by evaluating aspects of this research. The
Agency is particularly focusing on studies that evaluate the effects of
chlorpyrifos on infants and children from in utero and/or post-natal
exposures and on studies that evaluate population variability with
respect to response to chlorpyrifos. This review will encompass
selected human epidemiological data, in vivo data in laboratory animals
and in vitro studies. The Agency will be seeking comments from the SAP
on the following areas:
1. Interpretation of recent epidemiological studies associating in
utero and/or post-natal chlorpyrifos exposure with health outcomes;
2. Aspects of chlorpyrifos metabolism, such as differences in
paraoxonase 1 (PON 1) expression and activity, which affects population
variability with respect to the effects of chlorpyrifos and its oxon
metabolite; and
3. Cholinergic and non-cholinergic modes/mechanisms of toxicity
which are relevant to evaluating hazard and risk to infants and
children.
As part of this review, the Agency is evaluating the relevance of
animal studies conducted by different routes of administration (e.g.,
gavage or subcutaneous injection) for conducting human health risk
assessment to different age groups and by different exposure pathways.
C. FIFRA SAP Documents and Meeting Minutes
EPA's background paper, related supporting materials, charge/
questions to the FIFRA SAP, FIFRA SAP composition (i.e., members and ad
hoc members for this meeting), and the meeting agenda will be available
by late June 2008. In addition, the Agency may provide additional
background documents as the materials become available. You may obtain
electronic copies of these documents, and certain other related
documents that might be available electronically, at https://
www.regulations.gov and the FIFRA SAP homepage at https://www.epa.gov/
scipoly/sap.
The FIFRA SAP will prepare meeting minutes summarizing its
recommendations to the Agency approximately 90 days after the meeting.
The meeting minutes will be posted on the FIFRA SAP website or may be
obtained from the OPP Regulatory Public Docket at https://
www.regulations.gov.
List of Subjects
Environmental protection, Pesticides and pests.
Dated: April 10, 2008.
Elizabeth A. Resek,
Acting Director, Office of Science Coordination and Policy.
[FR Doc. E8-8399 Filed 4-17-08; 8:45 a.m.]
BILLING CODE 6560-50-S