Wildlife Services; Availability of a Supplemental Decision/Finding of No Significant Impact for Oral Rabies Vaccine Program, 20984-20986 [E7-8091]
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20984
Federal Register / Vol. 72, No. 81 / Friday April 27, 2007 / Notices
resources to carry out the submitted
plan.
Estimate of Burden: Public reporting
burden for this collection of information
is estimated to average 3 hours per
response.
Description of Respondents:
Businesses or other for profit
individuals.
Estimated Number of Respondents:
75.
Frequency of Responses: One time per
invention.
Estimated Total Annual Burden on
Respondents: 225 hours.
This data will be collected under the
authority of 44 U.S.C.3506(c)(2)(A).
Copies of this information collection
and related instructions can be obtained
without charge from June Blalock,
USDA, ARS, Office of Technology
Transfer by calling 301–504–5989.
Comments are invited on (a) Whether
the proposed collection of information
is necessary for the proper performance
of the functions of the agency, including
whether the information will have
practical utility; (b) the accuracy of the
agency’s estimate of the burden of the
proposed collection of information
including the validity of the
methodology and assumptions used; (c)
ways to enhance the quality, utility, and
clarity of the information to be
collected; and (d) ways to minimize the
burden of the collection of information
on those who are to respond, such as
through the use of appropriate
automated, electronic, mechanical, or
other technological collection
techniques. Comments may be sent to
USDA, ARS, Office of Technology
Transfer, 5601 Sunnyside Avenue,
Room 4–1174, Beltsville, Maryland
20705–5131. All responses to this notice
will be summarized and included in the
request for OMB approval. All
comments will also become a matter of
public record.
Richard J. Brenner,
Assistant Administrator.
[FR Doc. E7–8089 Filed 4–26–07; 8:45 am]
BILLING CODE 3410–03–P
DEPARTMENT OF AGRICULTURE
Animal and Plant Health Inspection
Service
cprice-sewell on PROD1PC66 with NOTICES
[Docket No. 01–009–9]
Wildlife Services; Availability of a
Supplemental Decision/Finding of No
Significant Impact for Oral Rabies
Vaccine Program
Animal and Plant Health
Inspection Service, USDA.
AGENCY:
VerDate Aug<31>2005
15:18 Apr 26, 2007
Jkt 211001
Notice of availability and
request for comments.
ACTION:
SUMMARY: We are advising the public
that we have prepared a proposed
decision/finding of no significant
impact relative to oral rabies
vaccination programs in several States.
Since the publication of our original
environmental assessment and decision/
finding of no significant impact in 2001,
we have prepared, and made available
to the public for comment, several
supplemental environmental
assessments and decisions/findings of
no significant impact in order to reflect
changes in the program. The decision/
finding of no significant impact made
available by this notice clarifies the term
‘‘contingency actions,’’ which was used
in a supplemental environmental
assessment we prepared in 2004, and
analyzes a type of contingency action
called trap-vaccinate-release that was
not analyzed as part of the proposed
action in the 2004 supplemental
environmental assessment. The new
decision/finding of no significant
impact is intended to facilitate planning
and interagency coordination in the
event of rabies outbreaks and to clearly
communicate to the public the actions
involved in the oral rabies vaccination
program.
DATES: We will consider all comments
that we receive on or before May 29,
2007. Unless we determine that new
substantial issues bearing on the
conduct of the oral rabies vaccine
programs have been raised by public
comments on this notice, the proposed
decision/finding of no significant
impact will become final and take effect
upon the close of the comment period.
ADDRESSES: You may submit comments
by either of the following methods:
• Federal eRulemaking Portal: Go to
https://www.regulations.gov, select
‘‘Animal and Plant Health Inspection
Service’’ from the agency drop-down
menu, then click ‘‘Submit.’’ In the
Docket ID column, select APHIS–2007–
0055 to submit or view public
comments and to view supporting and
related materials available
electronically. After the close of the
comment period, the docket can be
viewed using the ‘‘Advanced Search’’
function in Regulations.gov.
• Postal Mail/Commercial Delivery:
Please send four copies of your
comment (an original and three copies)
to Docket No. 01–009–9, Regulatory
Analysis and Development, PPD,
APHIS, Station 3A–03.8, 4700 River
Road Unit 118, Riverdale, MD 20737–
1238. Please state that your comment
refers to Docket No. 01–009–9.
PO 00000
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Fmt 4703
Sfmt 4703
Reading Room: You may read any
comments that we receive on this
docket in our reading room. The reading
room is located in room 1141 of the
USDA South Building, 14th Street and
Independence Avenue, SW.,
Washington, DC. Normal reading room
hours are 8 a.m. to 4:30 p.m., Monday
through Friday, except holidays. To be
sure someone is there to help you,
please call (202) 690–2817 before
coming.
Other Information: Additional
information about APHIS and its
programs is available on the Internet at
https://www.aphis.usda.gov.
FOR FURTHER INFORMATION CONTACT: Dr.
Dennis Slate, Rabies Program
Coordinator, Wildlife Services, APHIS,
59 Chenell Drive, Suite 2, Concord, NH
03301; (603) 223–9623. To obtain copies
of the documents discussed in this
notice, contact Tara Wilcox, Operational
Support Staff, WS, APHIS, 4700 River
Road Unit 87, Riverdale, MD 20737–
1234; phone (301) 734–7921, fax
(301)734–5157, or e-mail:
Tara.C.Wilcox@aphis.usda.gov. This
notice and the proposed decision/
finding of no significant impact are also
posted on the APHIS Web site at
https://www.aphis.usda.gov/
wildlife_damage/nepa.shtml.
SUPPLEMENTARY INFORMATION:
Background
The Wildlife Services (WS) program
in the Animal and Plant Health
Inspection Service (APHIS) cooperates
with Federal agencies, State and local
governments, and private individuals to
research and implement the best
methods of managing conflicts between
wildlife and human health and safety,
agriculture, property, and natural
resources. Wildlife-borne diseases that
can affect domestic animals and humans
are among the types of conflicts that
APHIS–WS addresses. Wildlife is the
dominant reservoir of rabies in the
United States.
On December 7, 2000, a notice was
published in the Federal Register (65
FR 76606–76607, Docket No. 00–045–1)
in which the Secretary of Agriculture
declared an emergency and transferred
funds from the Commodity Credit
Corporation to APHIS–WS for the
continuation and expansion of oral
rabies vaccination (ORV) programs to
address rabies in the States of Ohio,
New York, Vermont, Texas, and West
Virginia.
On March 7, 2001, we published a
notice in the Federal Register (66 FR
13697–13700, Docket No. 01–009–1) to
solicit public involvement in the
planning of a proposed cooperative
E:\FR\FM\27APN1.SGM
27APN1
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Federal Register / Vol. 72, No. 81 / Friday April 27, 2007 / Notices
program to stop the spread of rabies in
the States of New York, Ohio, Texas,
Vermont, and West Virginia. The notice
also stated that a small portion of
northeastern New Hampshire and the
western counties in Pennsylvania that
border Ohio could also be included in
these control efforts, and discussed the
possibility of APHIS–WS cooperating in
smaller-scale ORV projects in the States
of Florida, Massachusetts, Maryland,
New Jersey, Virginia, and Alabama. The
March 2001 notice contained detailed
information about the history of the
problems with raccoon rabies in eastern
States and with gray fox and coyote
rabies in Texas, along with information
about previous and ongoing efforts
using ORV baits in programs to prevent
the spread of the rabies variants or
‘‘strains’’ of concern.
Subsequently, on May 17, 2001, we
published in the Federal Register (66
FR 27489, Docket No. 01–009–2) a
notice in which we announced the
availability, for public review and
comment, of an environmental
assessment (EA) that examined the
potential environmental effects of the
ORV programs described in our March
2001 notice. We solicited comments on
the EA for 30 days ending on June 18,
2001. We received one comment by that
date. The comment was from an animal
protection organization and supported
APHIS’ efforts toward limiting or
eradicating rabies in wildlife
populations. The commenter did not,
however, support the use of lethal
monitoring methods or local
depopulation as part of an ORV
program.
On August 30, 2001, we published a
notice in the Federal Register (66 FR
45835–45836, Docket No. 01–009–3) in
which we advised the public of APHIS’
decision and finding of no significant
impact (FONSI) regarding the use of oral
vaccination to control specific rabies
virus strains in raccoons, gray foxes, and
coyotes in the United States. That
decision allows APHIS–WS to purchase
and distribute ORV baits, monitor the
effectiveness of the ORV programs, and
participate in implementing
contingency plans that may involve the
reduction of a limited number of local
target species populations through
lethal means (i.e., the preferred
alternative identified in the EA). The
decision was based upon the final EA,
which reflected our review and
consideration of the comments received
from the public in response to our
March 2001 and May 2001 notices and
information gathered during planning/
scoping meetings with State health
departments, other State and local
agencies, the Ontario Ministry of
VerDate Aug<31>2005
15:18 Apr 26, 2007
Jkt 211001
Natural Resources, and the Centers for
Disease Control and Prevention.
Following the August 2001
publication of our original decision/
FONSI, we determined there was a need
to expand the ORV programs to include
the States of Kentucky and Tennessee to
effectively stop the westward spread of
raccoon rabies. Accordingly, we
prepared a supplemental decision/
FONSI to document the potential effects
of expanding the programs. We
published a notice announcing the
availability of the supplemental
decision/FONSI in the Federal Register
on July 5, 2002 (67 FR 44797–44798,
Docket No. 01–009–4).
Following the publication of the
supplemental decision/FONSI in July
2002, we determined the need to further
expand the ORV program to include the
States of Georgia and Maine to
effectively prevent the westward and
northward spread of the rabies virus
across the United States and into
Canada. To facilitate planning,
interagency coordination, and program
management and to provide the public
with our analysis of potential individual
and cumulative impacts of the
expanded ORV programs, we prepared a
supplemental EA that addresses the
inclusion of Georgia and Maine, as well
as the 2002 inclusion of Kentucky and
Tennessee, in the ORV program. In
addition, we prepared a new decision/
FONSI based on the supplemental EA
that was published in the Federal
Register on June 30, 2003 (68 FR 38669–
38670, Docket No. 01–009–5).
Following publication of the 2003
supplemental EA and decision/FONSI,
we determined the need to further
expand the ORV program to include
portions of National Forest System
lands, excluding Wilderness Areas,
within several eastern States. The
National Forest System lands where
APHIS–WS involvement could be
expanded included the States of Maine,
New York, Vermont, New Hampshire,
Pennsylvania, Ohio, Virginia, West
Virginia, Tennessee, Kentucky,
Alabama, Georgia, Florida, North
Carolina, South Carolina,
Massachusetts, Maryland, and New
Jersey. Cooperative rabies surveillance
activities and/or baiting programs were
already being conducted on various
land classes, with the exception of
National Forest System lands, in many
of the aforementioned States. The
programs’ primary goals were to stop
the spread of a specific raccoon rabies
variant or ‘‘strain’’ of the rabies virus. If
not stopped, this strain could
potentially spread to much broader
areas of the United States and Canada
and cause substantial increases in
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Fmt 4703
Sfmt 4703
20985
public and domestic animal health costs
because of increased rabies exposures.
As numerous National Forest System
lands are located within current and
potential ORV barrier zones, it became
increasingly important to bait these
large land masses to effectively combat
this strain of the rabies virus. In
addition, we prepared a new decision/
FONSI based on the supplemental EA
that was published in the Federal
Register on February 20, 2004 (69 FR
7904–7905, Docket No. 01–009–6).
Following the 2004 supplemental EA
and decision/FONSI for expansion of
the ORV program to include portions of
National Forest System lands, we
determined the need to further expand
the ORV program to include 25 eastern
States (Maine, New York, Vermont, New
Hampshire, Pennsylvania, Ohio,
Virginia, West Virginia, Tennessee,
Kentucky, Alabama, Georgia, Florida,
North Carolina, South Carolina,
Massachusetts, Maryland, Connecticut,
Rhode Island, Delaware, Indiana,
Michigan, Mississippi, Louisiana and
New Jersey), the District of Columbia,
and Texas to effectively prevent the
westward and northward spread of the
rabies virus across the United States and
into Canada. In addition, we prepared a
new decision/FONSI based on the
supplemental EA that was published in
the Federal Register on September 23,
2004 (69 FR 56992–56993, Docket No.
01–009–7).
Following the 2004 supplemental EA
and decision/FONSI, we determined the
need to expand the ORV program to
include portions of National Forest
System lands, excluding Wilderness
Areas, within the same 25 eastern States
and the District of Columbia. As
numerous National Forest System lands
are located within current and potential
ORV barrier zones, it had become
increasingly important to bait these
large land masses to effectively combat
this strain of the rabies virus.
Accordingly, we prepared a
supplemental EA and decision/FONSI
that served to update program needs
and evaluate current data. Those
documents were made available through
a notice published in the Federal
Register on December 8, 2005 (70 FR
72977–72978, Docket No. 01–009–8).
The purpose of the new 2007
decision/FONSI that we are making
available through this notice is to clarify
the term ‘‘contingency actions,’’ which
is used in the 2004 supplemental EA.
Clarification should facilitate planning
and interagency coordination in the
event of rabies outbreaks and clearly
communicate to the public the actions
involved in the ORV program. In
addition, a type of contingency action
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27APN1
20986
Federal Register / Vol. 72, No. 81 / Friday April 27, 2007 / Notices
called trap-vaccinate-release (TVR) is
analyzed in the 2007 decision
document, as it was not analyzed as part
of the proposed action in the 2004
supplemental EA. Analysis of TVR in
the 2007 decision document does not
involve any substantially new
information and does not raise or create
any new substantive issues or
circumstances, thus APHIS–WS has
determined that there is no need to
supplement the 2004 EA with that
analysis. The new 2007 decision/FONSI
will serve to update and replace the
previous decision/FONSI, dated
September 9, 2004, for the 2004
supplemental EA.
The proposed decision/FONSI that is
the subject of this notice, as well as the
documents cited above that preceded it,
have been prepared in accordance with:
(1) The National Environmental Policy
Act of 1969 (NEPA), as amended (42
U.S.C. 4321 et seq.), (2) regulations of
the Council on Environmental Quality
for implementing the procedural
provisions of NEPA (40 CFR parts 1500–
1508), (3) USDA regulations
implementing NEPA (7 CFR part 1), and
(4) APHIS’s NEPA Implementing
Procedures (7 CFR part 372).
The decision/FONSI may be viewed
on the Regulations.gov Web site or in
our reading room. (Instructions for
accessing Regulations.gov and
information on the location and hours of
the reading room are provided under the
heading ADDRESSES at the beginning of
this notice.) In addition, copies may be
obtained by calling or writing to the
individual listed under FOR FURTHER
INFORMATION CONTACT.
Done in Washington, DC, this 23rd day of
April 2007.
Kevin Shea,
Acting Administrator, Animal and Plant
Health Inspection Service.
[FR Doc. E7–8091 Filed 4–26–07; 8:45 am]
BILLING CODE 3410–34–P
duty orders and findings with March
anniversary dates. In accordance with
the Department’s regulations, we are
initiating those administrative reviews.
EFFECTIVE DATE:
FOR FURTHER INFORMATION CONTACT:
Sheila E. Forbes, Office of AD/CVD
Operations, Customs Unit, Import
Administration, International Trade
Administration, U.S. Department of
Commerce, 14th Street and Constitution
Avenue, N.W., Washington, D.C. 20230,
telephone: (202) 482–4697.
SUPPLEMENTARY INFORMATION:
Background
DEPARTMENT OF COMMERCE
International Trade Administration
Initiation of Antidumping and
Countervailing Duty Administrative
Reviews
Import Administration,
International Trade Administration,
Department of Commerce.
SUMMARY: The Department of Commerce
(the Department) has received requests
to conduct administrative reviews of
various antidumping and countervailing
AGENCY:
The Department has received timely
requests, in accordance with 19 CFR
351.213(b)(2004), for administrative
reviews of various antidumping and
countervailing duty orders and findings
with March anniversary dates.
Initiation of Reviews:
In accordance with section 19 CFR
351.221(c)(1)(i), we are initiating
administrative reviews of the following
antidumping and countervailing duty
orders and findings. We intend to issue
the final results of these reviews not
later than March 31, 2008.
cprice-sewell on PROD1PC66 with NOTICES
Antidumping Duty Proceedings
Period to be Reviewed
BRAZIL: Certain Hot–Rolled Carbon Steel Flat Products.
A–351–828 .................................................................................................................................................................
Companhia Siderurgica Nacional.
Companhia Siderurgica de Tubarao.
BRAZIL: Certain Orange Juice.
A–351–840 .................................................................................................................................................................
Coinbra–Frutesp S.A..
Fischer S/A Agroindustria.
Sucocitrico Cutrale Ltda..
FRANCE: Stainless Steel Bar.
A–427–820 .................................................................................................................................................................
Ascometal S.A..
UGITECH S.A..
GERMANY: Stainless Steel Bar.
A–428–830 .................................................................................................................................................................
BGH Edelstahl Freital.
GmbH/BGH Edelstahl Lippendorf GmbH/BGH Edelstahl Lugau GmbH/BGH Edelstahl Siegen
GmbH.
Schmiedewerke Groditz GmbH.
ITALY: Stainless Steel Bar.
A–475–829 .................................................................................................................................................................
Acciaierie Valbruna S.p.A..
REPUBLIC OF KOREA: Certain Cut–to-Length Carbon Steel Plate1.
A–580–836 .................................................................................................................................................................
TC Steel.
DSEC, a subsidiary of Daewoo Shipbuilding & Marine Engineering.
THAILAND: Circular Welded Carbon Steel Pipes and Tubes.
A–549–502 .................................................................................................................................................................
Saha Thai Steel Pipe Company, Ltd..
THE PEOPLE’S REPUBLIC OF CHINA: Certain Tissue Paper Products2.
A–570–894 .................................................................................................................................................................
Foshan Sansico Co., Ltd..
Guangzhou Baxi Printing Products Limited.
Guilin Qifeng Paper Co., Ltd..
Guilin Samsam Paper Products Ltd..
Max Fortune Industrial Limited/Max Fortune (FETDE) Paper Products Co., Ltd..
PT Grafitecindo Ciptaprima.
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15:18 Apr 26, 2007
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3/1/06 - 2/28/07
8/24/05 - 2/28/07
3/1/06 - 2/28/07
3/1/06 - 2/28/07
3/1/06 - 2/28/07
2/1/06 - 1/31/07
3/1/06 - 2/28/07
3/1/06 - 2/28/07
Agencies
[Federal Register Volume 72, Number 81 (Friday, April 27, 2007)]
[Notices]
[Pages 20984-20986]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E7-8091]
-----------------------------------------------------------------------
DEPARTMENT OF AGRICULTURE
Animal and Plant Health Inspection Service
[Docket No. 01-009-9]
Wildlife Services; Availability of a Supplemental Decision/
Finding of No Significant Impact for Oral Rabies Vaccine Program
AGENCY: Animal and Plant Health Inspection Service, USDA.
ACTION: Notice of availability and request for comments.
-----------------------------------------------------------------------
SUMMARY: We are advising the public that we have prepared a proposed
decision/finding of no significant impact relative to oral rabies
vaccination programs in several States. Since the publication of our
original environmental assessment and decision/finding of no
significant impact in 2001, we have prepared, and made available to the
public for comment, several supplemental environmental assessments and
decisions/findings of no significant impact in order to reflect changes
in the program. The decision/finding of no significant impact made
available by this notice clarifies the term ``contingency actions,''
which was used in a supplemental environmental assessment we prepared
in 2004, and analyzes a type of contingency action called trap-
vaccinate-release that was not analyzed as part of the proposed action
in the 2004 supplemental environmental assessment. The new decision/
finding of no significant impact is intended to facilitate planning and
interagency coordination in the event of rabies outbreaks and to
clearly communicate to the public the actions involved in the oral
rabies vaccination program.
DATES: We will consider all comments that we receive on or before May
29, 2007. Unless we determine that new substantial issues bearing on
the conduct of the oral rabies vaccine programs have been raised by
public comments on this notice, the proposed decision/finding of no
significant impact will become final and take effect upon the close of
the comment period.
ADDRESSES: You may submit comments by either of the following methods:
Federal eRulemaking Portal: Go to https://
www.regulations.gov, select ``Animal and Plant Health Inspection
Service'' from the agency drop-down menu, then click ``Submit.'' In the
Docket ID column, select APHIS-2007-0055 to submit or view public
comments and to view supporting and related materials available
electronically. After the close of the comment period, the docket can
be viewed using the ``Advanced Search'' function in Regulations.gov.
Postal Mail/Commercial Delivery: Please send four copies
of your comment (an original and three copies) to Docket No. 01-009-9,
Regulatory Analysis and Development, PPD, APHIS, Station 3A-03.8, 4700
River Road Unit 118, Riverdale, MD 20737-1238. Please state that your
comment refers to Docket No. 01-009-9.
Reading Room: You may read any comments that we receive on this
docket in our reading room. The reading room is located in room 1141 of
the USDA South Building, 14th Street and Independence Avenue, SW.,
Washington, DC. Normal reading room hours are 8 a.m. to 4:30 p.m.,
Monday through Friday, except holidays. To be sure someone is there to
help you, please call (202) 690-2817 before coming.
Other Information: Additional information about APHIS and its
programs is available on the Internet at https://www.aphis.usda.gov.
FOR FURTHER INFORMATION CONTACT: Dr. Dennis Slate, Rabies Program
Coordinator, Wildlife Services, APHIS, 59 Chenell Drive, Suite 2,
Concord, NH 03301; (603) 223-9623. To obtain copies of the documents
discussed in this notice, contact Tara Wilcox, Operational Support
Staff, WS, APHIS, 4700 River Road Unit 87, Riverdale, MD 20737-1234;
phone (301) 734-7921, fax (301)734-5157, or e-mail:
Tara.C.Wilcox@aphis.usda.gov. This notice and the proposed decision/
finding of no significant impact are also posted on the APHIS Web site
at https://www.aphis.usda.gov/wildlife_damage/nepa.shtml.
SUPPLEMENTARY INFORMATION:
Background
The Wildlife Services (WS) program in the Animal and Plant Health
Inspection Service (APHIS) cooperates with Federal agencies, State and
local governments, and private individuals to research and implement
the best methods of managing conflicts between wildlife and human
health and safety, agriculture, property, and natural resources.
Wildlife-borne diseases that can affect domestic animals and humans are
among the types of conflicts that APHIS-WS addresses. Wildlife is the
dominant reservoir of rabies in the United States.
On December 7, 2000, a notice was published in the Federal Register
(65 FR 76606-76607, Docket No. 00-045-1) in which the Secretary of
Agriculture declared an emergency and transferred funds from the
Commodity Credit Corporation to APHIS-WS for the continuation and
expansion of oral rabies vaccination (ORV) programs to address rabies
in the States of Ohio, New York, Vermont, Texas, and West Virginia.
On March 7, 2001, we published a notice in the Federal Register (66
FR 13697-13700, Docket No. 01-009-1) to solicit public involvement in
the planning of a proposed cooperative
[[Page 20985]]
program to stop the spread of rabies in the States of New York, Ohio,
Texas, Vermont, and West Virginia. The notice also stated that a small
portion of northeastern New Hampshire and the western counties in
Pennsylvania that border Ohio could also be included in these control
efforts, and discussed the possibility of APHIS-WS cooperating in
smaller-scale ORV projects in the States of Florida, Massachusetts,
Maryland, New Jersey, Virginia, and Alabama. The March 2001 notice
contained detailed information about the history of the problems with
raccoon rabies in eastern States and with gray fox and coyote rabies in
Texas, along with information about previous and ongoing efforts using
ORV baits in programs to prevent the spread of the rabies variants or
``strains'' of concern.
Subsequently, on May 17, 2001, we published in the Federal Register
(66 FR 27489, Docket No. 01-009-2) a notice in which we announced the
availability, for public review and comment, of an environmental
assessment (EA) that examined the potential environmental effects of
the ORV programs described in our March 2001 notice. We solicited
comments on the EA for 30 days ending on June 18, 2001. We received one
comment by that date. The comment was from an animal protection
organization and supported APHIS' efforts toward limiting or
eradicating rabies in wildlife populations. The commenter did not,
however, support the use of lethal monitoring methods or local
depopulation as part of an ORV program.
On August 30, 2001, we published a notice in the Federal Register
(66 FR 45835-45836, Docket No. 01-009-3) in which we advised the public
of APHIS' decision and finding of no significant impact (FONSI)
regarding the use of oral vaccination to control specific rabies virus
strains in raccoons, gray foxes, and coyotes in the United States. That
decision allows APHIS-WS to purchase and distribute ORV baits, monitor
the effectiveness of the ORV programs, and participate in implementing
contingency plans that may involve the reduction of a limited number of
local target species populations through lethal means (i.e., the
preferred alternative identified in the EA). The decision was based
upon the final EA, which reflected our review and consideration of the
comments received from the public in response to our March 2001 and May
2001 notices and information gathered during planning/scoping meetings
with State health departments, other State and local agencies, the
Ontario Ministry of Natural Resources, and the Centers for Disease
Control and Prevention.
Following the August 2001 publication of our original decision/
FONSI, we determined there was a need to expand the ORV programs to
include the States of Kentucky and Tennessee to effectively stop the
westward spread of raccoon rabies. Accordingly, we prepared a
supplemental decision/FONSI to document the potential effects of
expanding the programs. We published a notice announcing the
availability of the supplemental decision/FONSI in the Federal Register
on July 5, 2002 (67 FR 44797-44798, Docket No. 01-009-4).
Following the publication of the supplemental decision/FONSI in
July 2002, we determined the need to further expand the ORV program to
include the States of Georgia and Maine to effectively prevent the
westward and northward spread of the rabies virus across the United
States and into Canada. To facilitate planning, interagency
coordination, and program management and to provide the public with our
analysis of potential individual and cumulative impacts of the expanded
ORV programs, we prepared a supplemental EA that addresses the
inclusion of Georgia and Maine, as well as the 2002 inclusion of
Kentucky and Tennessee, in the ORV program. In addition, we prepared a
new decision/FONSI based on the supplemental EA that was published in
the Federal Register on June 30, 2003 (68 FR 38669-38670, Docket No.
01-009-5).
Following publication of the 2003 supplemental EA and decision/
FONSI, we determined the need to further expand the ORV program to
include portions of National Forest System lands, excluding Wilderness
Areas, within several eastern States. The National Forest System lands
where APHIS-WS involvement could be expanded included the States of
Maine, New York, Vermont, New Hampshire, Pennsylvania, Ohio, Virginia,
West Virginia, Tennessee, Kentucky, Alabama, Georgia, Florida, North
Carolina, South Carolina, Massachusetts, Maryland, and New Jersey.
Cooperative rabies surveillance activities and/or baiting programs were
already being conducted on various land classes, with the exception of
National Forest System lands, in many of the aforementioned States. The
programs' primary goals were to stop the spread of a specific raccoon
rabies variant or ``strain'' of the rabies virus. If not stopped, this
strain could potentially spread to much broader areas of the United
States and Canada and cause substantial increases in public and
domestic animal health costs because of increased rabies exposures. As
numerous National Forest System lands are located within current and
potential ORV barrier zones, it became increasingly important to bait
these large land masses to effectively combat this strain of the rabies
virus. In addition, we prepared a new decision/FONSI based on the
supplemental EA that was published in the Federal Register on February
20, 2004 (69 FR 7904-7905, Docket No. 01-009-6).
Following the 2004 supplemental EA and decision/FONSI for expansion
of the ORV program to include portions of National Forest System lands,
we determined the need to further expand the ORV program to include 25
eastern States (Maine, New York, Vermont, New Hampshire, Pennsylvania,
Ohio, Virginia, West Virginia, Tennessee, Kentucky, Alabama, Georgia,
Florida, North Carolina, South Carolina, Massachusetts, Maryland,
Connecticut, Rhode Island, Delaware, Indiana, Michigan, Mississippi,
Louisiana and New Jersey), the District of Columbia, and Texas to
effectively prevent the westward and northward spread of the rabies
virus across the United States and into Canada. In addition, we
prepared a new decision/FONSI based on the supplemental EA that was
published in the Federal Register on September 23, 2004 (69 FR 56992-
56993, Docket No. 01-009-7).
Following the 2004 supplemental EA and decision/FONSI, we
determined the need to expand the ORV program to include portions of
National Forest System lands, excluding Wilderness Areas, within the
same 25 eastern States and the District of Columbia. As numerous
National Forest System lands are located within current and potential
ORV barrier zones, it had become increasingly important to bait these
large land masses to effectively combat this strain of the rabies
virus. Accordingly, we prepared a supplemental EA and decision/FONSI
that served to update program needs and evaluate current data. Those
documents were made available through a notice published in the Federal
Register on December 8, 2005 (70 FR 72977-72978, Docket No. 01-009-8).
The purpose of the new 2007 decision/FONSI that we are making
available through this notice is to clarify the term ``contingency
actions,'' which is used in the 2004 supplemental EA. Clarification
should facilitate planning and interagency coordination in the event of
rabies outbreaks and clearly communicate to the public the actions
involved in the ORV program. In addition, a type of contingency action
[[Page 20986]]
called trap-vaccinate-release (TVR) is analyzed in the 2007 decision
document, as it was not analyzed as part of the proposed action in the
2004 supplemental EA. Analysis of TVR in the 2007 decision document
does not involve any substantially new information and does not raise
or create any new substantive issues or circumstances, thus APHIS-WS
has determined that there is no need to supplement the 2004 EA with
that analysis. The new 2007 decision/FONSI will serve to update and
replace the previous decision/FONSI, dated September 9, 2004, for the
2004 supplemental EA.
The proposed decision/FONSI that is the subject of this notice, as
well as the documents cited above that preceded it, have been prepared
in accordance with: (1) The National Environmental Policy Act of 1969
(NEPA), as amended (42 U.S.C. 4321 et seq.), (2) regulations of the
Council on Environmental Quality for implementing the procedural
provisions of NEPA (40 CFR parts 1500-1508), (3) USDA regulations
implementing NEPA (7 CFR part 1), and (4) APHIS's NEPA Implementing
Procedures (7 CFR part 372).
The decision/FONSI may be viewed on the Regulations.gov Web site or
in our reading room. (Instructions for accessing Regulations.gov and
information on the location and hours of the reading room are provided
under the heading ADDRESSES at the beginning of this notice.) In
addition, copies may be obtained by calling or writing to the
individual listed under FOR FURTHER INFORMATION CONTACT.
Done in Washington, DC, this 23rd day of April 2007.
Kevin Shea,
Acting Administrator, Animal and Plant Health Inspection Service.
[FR Doc. E7-8091 Filed 4-26-07; 8:45 am]
BILLING CODE 3410-34-P