Wildlife Services; Availability of a Supplemental Decision/Finding of No Significant Impact for Oral Rabies Vaccine Program, 20984-20986 [E7-8091]

Download as PDF 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 Frm 00002 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 cprice-sewell on PROD1PC66 with NOTICES 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 PO 00000 Frm 00003 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 E:\FR\FM\27APN1.SGM 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. VerDate Aug<31>2005 15:18 Apr 26, 2007 Jkt 211001 PO 00000 Frm 00004 Fmt 4703 April 27, 2007. Sfmt 4703 E:\FR\FM\27APN1.SGM 27APN1 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
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