FIFRA Scientific Advisory Panel; Notice of Public Meeting, 8856-8859 [2012-3280]
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types of materials into ocean waters and
establishes a permit program for ocean
dumping. In addition the MPRSA
establishes the Marine Sanctuaries
Program, implemented by the National
Oceanographic and Atmospheric
Administration (NOAA), which requires
NOAA to designate ocean waters as
marine sanctuaries for the purpose of
preserving or restoring their
conservation, recreational, ecological or
aesthetic values. Pursuant to the Marine
Protection and Sanctuaries Act, NOAA
has not designated any marine
sanctuaries within the area covered by
the permit. The permit also prohibits
discharges to marine sanctuary areas.
Magnuson-Stevens Fishery
Management and Conservation Act.
EPA has determined that reissuance of
this general permit is not likely to
adversely affect Essential Fish Habitat
established under the 1996 amendments
to the Magnuson-Stevens Fishery
Management and Conservation Act. In a
letter dated June 17, 2011, National
Marine Fisheries Service (NMFS)
concurred with the determination that
issuance of the permit has no adverse
effect to Essential Fish Habitat.
Coastal Zone Management Act. EPA
has determined that the activities which
are authorized by this permit are
consistent with the local and state
Coastal Zone Management Plans. The
State of Texas issued a letter of
consistency on January 26, 2012. It
should be noted that decisions to allow
oil and gas exploration and production
in the territorial seas are made by the
State of Texas and not the EPA.
State Certification. Under section
401(a)(1) of the CWA. EPA may not
issue an NPDES permit until the State
in which the discharge will originate
grants or waives certification to ensure
compliance with appropriate
requirements of the Act and State law.
Section 301(b)(1)(C) of the CWA
requires that NPDES permits contain
conditions that ensure compliance with
applicable state water quality standards
or limitations. The permit contains
limitations intended to ensure
compliance with Texas Water Quality
Standards and the corresponding
implementation guidance. The Texas
Railroad Commission issued the 401
certification on January 26, 2012.
Paperwork Reduction Act. The
information collection required by this
permit has been approved by the Office
of Management and Budget (OMB)
under the provisions of the Paperwork
Reduction Act, 44 U.S.C. 3501 et seq.,
and assigned OMB control numbers
2040–0086 (NPDES permit application)
and 2040–0004 (discharge monitoring
reports).
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This reissued permit requires
reporting and application requirements
for new facilities to comply with cooling
water intake structure requirements and
therefore it requires more reporting
burdens for new facilities from those
under the previous general permit.
Since this permit is very similar in
reporting and application requirements
in discharges which are required to be
monitored as the Western Gulf of
Mexico Outer Continental Shelf (OCS)
general permit (GMG290000) which also
has cooling water intake structure
requirements, the paperwork burdens
are expected to be nearly identical. EPA
estimated it would take an affected
facility three hours to prepare the
request for coverage and 3 hours per
month to prepare discharge monitoring
reports. It is estimated that the time
required to prepare the request for
coverage and discharge monitoring
reports for this permit will be the same.
A new facility may need more time to
prepare information for cooling water
intake structure requirements. This
permit requires electronic reporting for
discharge monitoring reports, and it will
save some reporting time.
However, the alternative to obtaining
authorization to discharge under this
general permit is to obtain an individual
permit. The burden of obtaining
authorization to discharge under the
general permit is expected to be
significantly less than the burden of
obtaining an individual permit.
Regulatory Flexibility Act. The
Regulatory Flexibility Act, 5 U.S.C. 601
et seq, requires that EPA prepare a
regulatory flexibility analysis for
regulations that have a significant
impact on a substantial number of small
entities. The permit renewal issued
today is not a ‘‘rule’’ subject to the
Regulatory Flexibility Act. EPA
prepared a regulatory flexibility
analysis, however, on the promulgation
of the Offshore Subcategory guidelines
on which many of the permit’s effluent
limitations are based. That analysis has
shown that issuance of this permit
would not have a significant impact on
a substantial number of small entities.
Authority: Clean Water Act, 33 U.S.C.
1251 et seq.
Dated: February 8, 2012.
William K. Honker,
Acting Director, Water Quality Protection
Division, EPA Region 6.
[FR Doc. 2012–3584 Filed 2–14–12; 8:45 am]
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ENVIRONMENTAL PROTECTION
AGENCY
[EPA–HQ–OPP–2012–0040; FRL–9335–5]
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 scientific issues concerning
chlorpyrifos health effects.
DATES: The meeting will be held on
April 10–13, 2012, from approximately
9 a.m. to 5:30 p.m.
Comments. The Agency encourages
that written comments be submitted by
March 27, 2012, and requests for oral
comments be submitted by April 3,
2012. However, written comments and
requests to make oral comments may be
submitted until the date of the meeting,
but anyone submitting written
comments after March 27, 2012, should
contact the Designated Federal Official
(DFO) listed under FOR FURTHER
INFORMATION CONTACT. For additional
instructions, see Unit I.C. of the
SUPPLEMENTARY INFORMATION.
Nominations. Nominations of
candidates to serve as ad hoc members
of FIFRA SAP for this meeting should
be provided on or before February 29,
2012.
Webcast. This meeting may be
webcast. Please refer to the FIFRA SAP’s
Web site, https://www.epa.gov/scipoly/
sap for information on how to access the
webcast. Please note that the webcast is
a supplementary public process
provided only for convenience. If
difficulties arise resulting in webcasting
outages, the meeting will continue as
planned.
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
the Environmental Protection Agency,
Conference Center, Lobby Level, One
Potomac Yard (South Bldg.), 2777 S.
Crystal Dr., Arlington, VA 22202.
Comments. Submit your comments,
identified by docket identification (ID)
number EPA–HQ–OPP–2012–0040, by
one of the following methods:
SUMMARY:
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• 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
Facility ’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–2012–
0040. 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 Web site 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 email comment directly
to EPA without going through
regulations.gov, your email address will
be automatically captured and included
as part of the comment that is placed in
the docket and made available on the
Internet. If you submit an electronic
comment, EPA recommends that you
include your name and other contact
information in the body of your
comment and with any disk or CD–ROM
you submit. If EPA cannot read your
comment due to technical difficulties
and cannot contact you for clarification,
EPA may not be able to consider your
comment. Electronic files should avoid
the use of special characters, any form
of encryption, and be free of any defects
or viruses.
Docket: All documents in the docket
are listed in the docket index available
at https://www.regulations.gov. Although
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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.
Nominations, requests to present oral
comments, and requests for special
accommodations. Submit nominations
to serve as ad hoc members of 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: Fred
Jenkins, Jr., DFO, Office of Science
Coordination and Policy (7201M),
Environmental Protection Agency, 1200
Pennsylvania Ave. NW., Washington,
DC 20460–0001; telephone number:
(202) 564–3327; fax number: (202) 564–
8382; email address:
jenkins.fred@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
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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–2012–0040 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
ADDRESSES, no later than March 27,
2012, to provide FIFRA SAP the time
necessary to consider and review the
written comments. Written comments
are accepted until the date of the
meeting, but anyone submitting written
comments after March 27, 2012, should
contact the DFO listed under FOR
FURTHER INFORMATION CONTACT. Anyone
submitting written comments at the
meeting should bring 30 copies for
distribution to 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 April 3, 2012, 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 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
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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 open and on a firstcome basis.
4. Request for nominations to serve as
ad hoc members of FIFRA SAP for this
meeting. As part of a broader process for
developing a pool of candidates for each
meeting, FIFRA SAP staff routinely
solicits the stakeholder community for
nominations of prospective candidates
for service as ad hoc members of 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: Cholinergic
and non-cholinergic mechanisms,
cholinesterase inhibition,
developmental neurotoxicity,
epidemiology (particularly
reproductive/developmental,
environmental), exposure assessment of
pesticides (both residential and
agricultural worker), human
biomonitoring data and interpretation of
such data, human health risk
assessment, mode of action analysis—
people with experience with the mode
of action framework, and
organophosphate pesticides
pharmacokinetics. Nominees should be
scientists who have sufficient
professional qualifications, 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 February 29, 2012. 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
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
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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 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 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 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 Web
site 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 FIFRA SAP
FIFRA SAP serves as the primary
scientific peer review mechanism of
EPA’s Office of Chemical Safety and
Pollution Prevention (OCSPP) and is
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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. FIFRA SAP is a
Federal advisory committee established
in 1975 under FIFRA that operates in
accordance with requirements of the
Federal Advisory Committee Act. 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 SAP on an ad hoc basis to assist in
reviews conducted by the SAP. As a
peer review mechanism, FIFRA SAP
provides comments, evaluations and
recommendations to improve the
effectiveness and quality of analyses
made by Agency scientists. Members of
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
Chlorpyrifos (0,0-diethyl-0-3,5,6trichloro-2-pyridyl phosphorothioate) is
a broad-spectrum, chlorinated
organophosphate (OP) insecticide. Like
other OPs, chlorpyrifos binds to and
phosphorylates the enzyme
acetylcholinesterase (AChE) in both the
central (brain) and peripheral nervous
systems. This can lead to accumulation
of acetylcholine and, ultimately, at
sufficiently high doses, to clinical signs
of toxicity. In 2011, the Agency released
a preliminary human health risk
assessment for chlorpyrifos. The focus
of this assessment was on the
cholinesterase (ChE) inhibiting potential
of chlorpyrifos. Consistent with this
focus, EPA evaluated the extensive
database of ChE data for multiple
lifestages and selected points of
departure (PoDs) based on consideration
of all quality and reliable data. There is,
however, a growing body of literature
with laboratory animals (rats and mice)
indicating that gestational and/or early
postnatal exposure to chlorpyrifos may
cause persistent effects into adulthood.
The results of both in vivo and in vitro
studies on chlorpyrifos have led some
research groups to propose that changes
in brain connectivity and/or
neurochemistry may underlie these
changes into adulthood. In addition,
there are epidemiology studies
evaluating pre- and post-natal
chlorpyrifos or other OP exposure in
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mother-infant pairs that have reported
associations with birth outcomes,
childhood neurobehavioral and
neurodevelopment outcomes in the
offspring when evaluated in neonates,
infants, and young children.
In 2008, the FIFRA Scientific
Advisory Panel (SAP) reviewed a draft
science issue paper on the human
health effects of chlorpyrifos which
provided a preliminary review of the
scientific literature on experimental
toxicology and epidemiology studies
available at that time. In 2010, the
Agency developed a draft ‘‘Framework
for Incorporating Human Epidemiologic
& Incident Data in Health Risk
Assessment’’ which provides the
conceptual foundation for evaluating
multiple lines of scientific evidence in
the context of the understanding of the
adverse outcome pathway (or mode of
action). This draft framework uses
modified Bradford Hill Criteria to
evaluate the sufficiency of evidence to
establish key events within a mode of
action(s) and explicitly considers such
concepts as strength, consistency, dose
response, temporal concordance and
biological plausibility. Since the 2008
SAP on chlorpyrifos, the Agency has
performed further analyses on the
existing and new epidemiology results
in mothers and children, available
biomonitoring data, and experimental
toxicology studies evaluating proposed
adverse outcome pathways in the
context of human health risk
assessment. Specifically, the Agency is
evaluating available literature on the
potential for chlorpyrifos to cause long
term adverse effects from early life
exposure, in vivo and in vitro studies
evaluating mechanistic aspects of
chlorpyrifos, and the potential for
adverse effects below doses established
from ChE inhibition that are used for
regulatory purposes. At this time, the
Agency is working towards a weight of
evidence evaluation integrating the
epidemiology studies with the
experimental toxicology studies for the
neurodevelopmental outcomes. This
analysis is complex and multifaceted as
it involves different lines of scientific
evidence (i.e., in vivo and in vitro
experimental toxicology studies,
explicit consideration of adverse
outcome pathways, exposure,
epidemiology, and biomonitoring data).
As such, the Agency believes that peer
review on the status of the current
analysis is important.
C. FIFRA SAP Documents and Meeting
Minutes
EPA’s background paper, related
supporting materials, charge/questions
to FIFRA SAP, FIFRA SAP composition
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(i.e., members and ad hoc members for
this meeting), and the meeting agenda
will be available by approximately midMarch. 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.
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 Web site or
may be obtained from the OPP
Regulatory Public Docket at https://
www.regulations.gov.
Environmental protection, Pesticides
and pests.
Dated: February 2, 2012.
Frank Sanders,
Director, Office of Science Coordination and
Policy.
[FR Doc. 2012–3280 Filed 2–14–12; 8:45 am]
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ENVIRONMENTAL PROTECTION
AGENCY
[FRL–9632–4]
National Advisory Council for
Environmental Policy and Technology
Environmental Protection
Agency (EPA).
ACTION: Cancellation and Rescheduling
of National Advisory Council for
Environmental Policy and Technology
(NACEPT) Committee Meeting.
AGENCY:
EPA announced in the
Federal Register on January 12, 2012
[FRL–9617–7] a National Advisory
Council for Environmental Policy and
Technology (NACEPT) Meeting to be
held at the EPA Potomac Yard
Conference Center, One Potomac Yard,
2777 S. Crystal Drive, Arlington, VA
22202. Under the Federal Advisory
Committee Act, Public Law 92463, EPA
gives notice of cancellation and
rescheduling of that public meeting for
the National Advisory Council for
Environmental Policy and Technology
(NACEPT). NACEPT provides advice to
the EPA Administrator on a broad range
of environmental policy, technology,
and management issues. NACEPT
members represent academia, industry,
non-governmental organizations, and
SUMMARY:
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local, state, and tribal governments. The
purpose of this meeting is to begin
developing recommendations to the
Administrator regarding actions that
EPA can take in response to the
National Academy of Sciences Report
on ‘‘Incorporating Sustainability in the
U.S. Environmental Protection Agency.’’
A copy of the agenda for the meeting
will be posted at https://
www.epa.govofacmo/nacept/calnacept.htm.
NACEPT has cancelled the twoday public meeting scheduled for
February 13, 2012, from February 14,
2012. NACEPT will now hold the twoday public meeting on Monday, March
26, 2012, from 9 a.m. to 5:30 p.m. (EST)
and Tuesday, March 27, 2012 from 8:30
a.m. to 2 p.m. (EST).
DATES:
The meeting will be held at
the EPA East Building Room 1153, 1201
Constitution Avenue NW., Washington,
DC 20004.
ADDRESSES:
List of Subjects
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FOR FURTHER INFORMATION CONTACT:
Mark Joyce, Acting Designated Federal
Officer, joyce.mark@epa.gov, (202) 564–
2130, U.S. EPA, Office of Federal
Advisory Committee Management and
Outreach (1601M), 1200 Pennsylvania
Avenue NW., Washington, DC 20460.
Requests
to make oral comments or to provide
written comments for the March 26–27,
2012, NACEPT meeting should be sent
to Eugene Green at
green.eugene@epa.gov by Monday,
March 19, 2012. The meeting is open to
the public, with limited seating
available on a first-come, first-served
basis. Members of the public wishing to
attend should contact Eugene Green at
green.eugene@epa.gov or (202) 564–
2432 by March 19, 2012.
Meeting Access: Information regarding
accessibility and/or accommodations for
individuals with disabilities should be
directed to Eugene Green at the email
address or phone number listed above.
To ensure adequate time for processing,
please make requests for
accommodations at least 10 days prior
to the meeting.
SUPPLEMENTARY INFORMATION:
Dated: February 7, 2012.
Mark Joyce,
Acting Designated Federal Officer.
[FR Doc. 2012–3533 Filed 2–14–12; 8:45 am]
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Agencies
[Federal Register Volume 77, Number 31 (Wednesday, February 15, 2012)]
[Notices]
[Pages 8856-8859]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2012-3280]
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ENVIRONMENTAL PROTECTION AGENCY
[EPA-HQ-OPP-2012-0040; FRL-9335-5]
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 scientific issues concerning chlorpyrifos health
effects.
DATES: The meeting will be held on April 10-13, 2012, from
approximately 9 a.m. to 5:30 p.m.
Comments. The Agency encourages that written comments be submitted
by March 27, 2012, and requests for oral comments be submitted by April
3, 2012. However, written comments and requests to make oral comments
may be submitted until the date of the meeting, but anyone submitting
written comments after March 27, 2012, should contact the Designated
Federal Official (DFO) listed under FOR FURTHER INFORMATION CONTACT.
For additional instructions, see Unit I.C. of the SUPPLEMENTARY
INFORMATION.
Nominations. Nominations of candidates to serve as ad hoc members
of FIFRA SAP for this meeting should be provided on or before February
29, 2012.
Webcast. This meeting may be webcast. Please refer to the FIFRA
SAP's Web site, https://www.epa.gov/scipoly/sap for information on how
to access the webcast. Please note that the webcast is a supplementary
public process provided only for convenience. If difficulties arise
resulting in webcasting outages, the meeting will continue as planned.
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 the Environmental Protection
Agency, Conference Center, Lobby Level, One Potomac Yard (South Bldg.),
2777 S. Crystal Dr., Arlington, VA 22202.
Comments. Submit your comments, identified by docket identification
(ID) number EPA-HQ-OPP-2012-0040, by one of the following methods:
[[Page 8857]]
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 Facility '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-
2012-0040. 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 Web site 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 email comment directly to EPA without
going through regulations.gov, your email address will be automatically
captured and included as part of the comment that is placed in the
docket and made available on the Internet. If you submit an electronic
comment, EPA recommends that you include your name and other contact
information in the body of your comment and with any disk or CD-ROM you
submit. If EPA cannot read your comment due to technical difficulties
and cannot contact you for clarification, EPA may not be able to
consider your comment. Electronic files should avoid the use of special
characters, any form of encryption, and be free of any defects or
viruses.
Docket: All documents in the docket are listed in the docket index
available at https://www.regulations.gov. 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.
Nominations, requests to present oral comments, and requests for
special accommodations. Submit nominations to serve as ad hoc members
of 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: Fred Jenkins, Jr., DFO, Office of
Science Coordination and Policy (7201M), Environmental Protection
Agency, 1200 Pennsylvania Ave. NW., Washington, DC 20460-0001;
telephone number: (202) 564-3327; fax number: (202) 564-8382; email
address: jenkins.fred@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-2012-0040 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 ADDRESSES, no later than March 27,
2012, to provide FIFRA SAP the time necessary to consider and review
the written comments. Written comments are accepted until the date of
the meeting, but anyone submitting written comments after March 27,
2012, should contact the DFO listed under FOR FURTHER INFORMATION
CONTACT. Anyone submitting written comments at the meeting should bring
30 copies for distribution to 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 April 3, 2012, 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
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
[[Page 8858]]
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 open and
on a first-come basis.
4. Request for nominations to serve as ad hoc members of FIFRA SAP
for this meeting. As part of a broader process for developing a pool of
candidates for each meeting, FIFRA SAP staff routinely solicits the
stakeholder community for nominations of prospective candidates for
service as ad hoc members of 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: Cholinergic and non-cholinergic mechanisms, cholinesterase
inhibition, developmental neurotoxicity, epidemiology (particularly
reproductive/developmental, environmental), exposure assessment of
pesticides (both residential and agricultural worker), human
biomonitoring data and interpretation of such data, human health risk
assessment, mode of action analysis--people with experience with the
mode of action framework, and organophosphate pesticides
pharmacokinetics. Nominees should be scientists who have sufficient
professional qualifications, 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 February
29, 2012. 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 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 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 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 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 Web site 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 FIFRA SAP
FIFRA SAP serves as the primary scientific peer review mechanism of
EPA's Office of Chemical Safety and Pollution Prevention (OCSPP) 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. FIFRA SAP is a Federal advisory committee established in
1975 under FIFRA that operates in accordance with requirements of the
Federal Advisory Committee Act. 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 SAP on an ad hoc basis to assist in reviews
conducted by the SAP. As a peer review mechanism, FIFRA SAP provides
comments, evaluations and recommendations to improve the effectiveness
and quality of analyses made by Agency scientists. Members of 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
Chlorpyrifos (0,0-diethyl-0-3,5,6-trichloro-2-pyridyl
phosphorothioate) is a broad-spectrum, chlorinated organophosphate (OP)
insecticide. Like other OPs, chlorpyrifos binds to and phosphorylates
the enzyme acetylcholinesterase (AChE) in both the central (brain) and
peripheral nervous systems. This can lead to accumulation of
acetylcholine and, ultimately, at sufficiently high doses, to clinical
signs of toxicity. In 2011, the Agency released a preliminary human
health risk assessment for chlorpyrifos. The focus of this assessment
was on the cholinesterase (ChE) inhibiting potential of chlorpyrifos.
Consistent with this focus, EPA evaluated the extensive database of ChE
data for multiple lifestages and selected points of departure (PoDs)
based on consideration of all quality and reliable data. There is,
however, a growing body of literature with laboratory animals (rats and
mice) indicating that gestational and/or early postnatal exposure to
chlorpyrifos may cause persistent effects into adulthood. The results
of both in vivo and in vitro studies on chlorpyrifos have led some
research groups to propose that changes in brain connectivity and/or
neurochemistry may underlie these changes into adulthood. In addition,
there are epidemiology studies evaluating pre- and post-natal
chlorpyrifos or other OP exposure in
[[Page 8859]]
mother-infant pairs that have reported associations with birth
outcomes, childhood neurobehavioral and neurodevelopment outcomes in
the offspring when evaluated in neonates, infants, and young children.
In 2008, the FIFRA Scientific Advisory Panel (SAP) reviewed a draft
science issue paper on the human health effects of chlorpyrifos which
provided a preliminary review of the scientific literature on
experimental toxicology and epidemiology studies available at that
time. In 2010, the Agency developed a draft ``Framework for
Incorporating Human Epidemiologic & Incident Data in Health Risk
Assessment'' which provides the conceptual foundation for evaluating
multiple lines of scientific evidence in the context of the
understanding of the adverse outcome pathway (or mode of action). This
draft framework uses modified Bradford Hill Criteria to evaluate the
sufficiency of evidence to establish key events within a mode of
action(s) and explicitly considers such concepts as strength,
consistency, dose response, temporal concordance and biological
plausibility. Since the 2008 SAP on chlorpyrifos, the Agency has
performed further analyses on the existing and new epidemiology results
in mothers and children, available biomonitoring data, and experimental
toxicology studies evaluating proposed adverse outcome pathways in the
context of human health risk assessment. Specifically, the Agency is
evaluating available literature on the potential for chlorpyrifos to
cause long term adverse effects from early life exposure, in vivo and
in vitro studies evaluating mechanistic aspects of chlorpyrifos, and
the potential for adverse effects below doses established from ChE
inhibition that are used for regulatory purposes. At this time, the
Agency is working towards a weight of evidence evaluation integrating
the epidemiology studies with the experimental toxicology studies for
the neurodevelopmental outcomes. This analysis is complex and
multifaceted as it involves different lines of scientific evidence
(i.e., in vivo and in vitro experimental toxicology studies, explicit
consideration of adverse outcome pathways, exposure, epidemiology, and
biomonitoring data). As such, the Agency believes that peer review on
the status of the current analysis is important.
C. FIFRA SAP Documents and Meeting Minutes
EPA's background paper, related supporting materials, charge/
questions to FIFRA SAP, FIFRA SAP composition (i.e., members and ad hoc
members for this meeting), and the meeting agenda will be available by
approximately mid-March. 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.
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 Web site or may be
obtained from the OPP Regulatory Public Docket at https://www.regulations.gov.
List of Subjects
Environmental protection, Pesticides and pests.
Dated: February 2, 2012.
Frank Sanders,
Director, Office of Science Coordination and Policy.
[FR Doc. 2012-3280 Filed 2-14-12; 8:45 am]
BILLING CODE 6560-50-P