Oral Rabies Vaccine Program; Availability of an Environmental Assessment, 32700-32701 [2019-14536]
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Federal Register / Vol. 84, No. 131 / Tuesday, July 9, 2019 / Notices
khammond on DSKBBV9HB2PROD with NOTICES
displays a currently valid OMB control
number and the agency informs
potential persons who are to respond to
the collection of information that such
persons are not required to respond to
the collection of information unless it
displays a currently valid OMB control
number.
Agricultural Marketing Service
Title: Local Food Directories and
Survey.
OMB Control Number: 0581–0169.
Summary of Collection: The primary
legislative basis for conducting farmer’s
market research is the Agricultural
Marketing Act of 1946 (7 U.S.C. 1621–
1627). In addition, the Farmer-toConsumer Direct Marketing Act of 1976
supports USDA’s work to enhance the
effectiveness of direct marketing, such
as the development of modern farmers
markets, the development of On-Farm
Markets, Community Supported
Agriculture (CSA) and Food Hubs. The
Marketing Services Division (MSD),
Agricultural Marketing Service (AMS)
identifies marketing opportunities,
provides analysis to help take advantage
of those opportunities and develops and
evaluates solutions including improving
farmers markets and other direct-toconsumer marketing activities. Markets
are maintained by State Departments of
Agriculture, local public authorities,
grower organizations and non-profit
organizations.
Need and Use of the Information: The
information will be collected using the
form TM–6 ‘‘Farmers’ Market Directory
and Survey,’’ the On-Farm Market
Questionnaire, CSA Questionnaire, and
the Food Hub Questionnaire. Each
survey/questionnaire collects the data
necessary to populate the USDA
National Farmers Market Directory, and
the other three direct to customer
directories. Combining the collections
will reduce the number of times that it
seeks to make contact with market
managers. Participating market
managers are invited to participate in an
optional National Farmers Market
Managers Survey evaluating the farmer’s
market sector. These markets represent
a varied range of sizes, geographical
locations, types, ownership, structure,
and will provide a valid overview of
farmers markets in the United States.
Information such as the size of market’s,
operating times and days, retail and
wholesale sales, management structure,
and rules and regulations governing the
markets are all important questions that
need to be answered in the design of a
new market. The information developed
by the Farmer’s Market Survey will
support better designs, development
techniques, and operating methods for
VerDate Sep<11>2014
17:47 Jul 08, 2019
Jkt 247001
modern farmers markets and outline
improvements that can be applied to
revitalize existing markets. The three
direct marketing channel directories
along with the National Farmer’s Market
Directory website will provide
synergies, give customers a one stop
shopping website for a wide variety of
locally produced directly marketed farm
products, and provide a free advertising
venue for agricultural enterprise
managers seeking to diversify their
farming operation by marketing directly
to customers.
Description of Respondents: Not-forprofit institutions.
Number of Respondents: 8,700.
Frequency of Responses: Reporting:
On occasion.
Total Burden Hours: 2,069.
Kimble Brown,
Departmental Information Collection
Clearance Officer.
[FR Doc. 2019–14492 Filed 7–8–19; 8:45 am]
BILLING CODE 3410–02–P
DEPARTMENT OF AGRICULTURE
Animal and Plant Health Inspection
Service
[Docket No. APHIS–2019–0034]
Oral Rabies Vaccine Program;
Availability of an Environmental
Assessment
Animal and Plant Health
Inspection Service, USDA.
ACTION: Notice of availability and
request for comments.
AGENCY:
We are advising the public
that the Animal and Plant Health
Inspection Service has prepared an
environmental assessment (EA) relative
to an oral rabies vaccination (ORV)
program in Maine, New Hampshire,
New York, Ohio, Tennessee, Texas,
Vermont, Virginia, and West Virginia.
The EA analyzes the proposed
expanded use of ONRAB vaccine-baits
throughout the ORV distribution zone in
those States in cooperation with the
U.S. Forest Service. The proposed
expanded ONRAB vaccine distribution
is necessary as a higher level of
population immunity in raccoons is
desired in order to maximize the
effectiveness of ORV programs. We are
making the EA available to the public
for review and comment.
DATES: We will consider all comments
that we receive on or before August 8,
2019.
ADDRESSES: You may submit comments
by either of the following methods:
SUMMARY:
PO 00000
Frm 00002
Fmt 4703
Sfmt 4703
• Federal eRulemaking Portal: Go to
https://www.regulations.gov/#!docket
Detail;D=APHIS-2019-0034.
• Postal Mail/Commercial Delivery:
Send your comment to Docket No.
APHIS–2019–0034, Regulatory Analysis
and Development, PPD, APHIS, Station
3A–03.8, 4700 River Road Unit 118,
Riverdale, MD 20737–1238.
The supplemental environmental
assessment and any comments we
receive may be viewed at https://
www.regulations.gov/#!docketDetail;D=
APHIS-2019-0034 or in our reading
room, which 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) 799–7039 before
coming.
This notice and the supplemental
environmental assessment are also
posted on the Animal and Plant Health
Inspection Service website at https://
www.aphis.usda.gov/regulations/ws/ws_
nepa_environmental_documents.shtml.
FOR FURTHER INFORMATION CONTACT: Mr.
Richard Chipman, Rabies Program
Coordinator, Wildlife Services, APHIS,
59 Chennell Drive, Suite 7, Concord, NH
03301; (603) 223–9623; email:
richard.b.chipman@usda.gov. To obtain
copies of the supplemental
environmental assessment, contact Ms.
Beth Kabert, Staff Wildlife Biologist,
Wildlife Services, 59 Chennell Drive,
Suite 7, Concord, NH 03301; (908) 442–
6761; fax (603) 229–0502; email:
beth.e.kabert@usda.gov.
SUPPLEMENTARY INFORMATION: The
Wildlife Services (WS) program in the
Animal and Plant Health Inspection
Service 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 WS
addresses. Wildlife is the dominant
reservoir of rabies in the United States.
WS conducts an oral rabies
vaccination (ORV) program to control
the spread of rabies. The ORV program
has utilized a vaccinia-rabies
glycoprotein (V–RG) vaccine. WS’ use of
the V–RG vaccine has resulted in
several notable accomplishments,
including the elimination of canine
rabies from sources in Mexico, the
successful control of gray fox rabies
virus variant in western Texas, and the
E:\FR\FM\09JYN1.SGM
09JYN1
khammond on DSKBBV9HB2PROD with NOTICES
Federal Register / Vol. 84, No. 131 / Tuesday, July 9, 2019 / Notices
prevention of any appreciable spread of
raccoon rabies in the eastern United
States. While the prevention of any
appreciable spread of raccoon rabies in
the eastern United States represents a
major accomplishment in rabies
management, the V–RG vaccine has not
been effective in eliminating raccoon
rabies from high-risk spread corridors.
This fact prompted WS to evaluate
rabies vaccines capable of producing
higher levels of population immunity
against raccoon rabies to better control
the spread of this disease.
Since 2011, WS has been conducting
field trials to study the immunogenicity
and safety of an experimental oral rabies
vaccine, a human adenovirus type 5
rabies glycoprotein recombinant vaccine
called ONRAB (produced by Artemis
Technologies Inc., Guelph, Ontario,
Canada). The field trials began in
portions of West Virginia, including
U.S. Department of Agriculture Forest
Service National Forest System lands.
Beginning in 2012, WS expanded
field trials into portions of New
Hampshire, New York, Ohio, Vermont,
and new areas of West Virginia,
including National Forest System lands,
in order to further assess the
immunogenicity of ONRAB in raccoons
and skunks for raccoon rabies virus
variant.
WS is now proposing to further
expand ONRAB vaccine distribution to
enhance rabies management in the
United States to protect human and
animal health and reduce social costs.
The proposed expanded use of ONRAB
is necessary as a higher level of
population immunity in raccoons is
desired in order to maximize the
effectiveness of ORV programs, and the
RABORAL V–RG vaccine has not
produced sufficient levels of population
immunity in skunks (primarily striped
skunks) in the wild at the current dose.
WS has prepared an environmental
assessment (EA) in which we analyze
the proposed expanded use of ONRAB
vaccine-baits throughout the ORV
distribution zone in Maine, New
Hampshire, New York, Ohio, Tennessee,
Texas, Vermont, Virginia, and West
Virginia in cooperation with the U.S.
Forest Service. This EA will supersede
the 2012 EA ‘‘Field Trial of an
Experimental Rabies Vaccine, Human
Adenovirus Type 5 Vector in New
Hampshire, New York, Ohio, Vermont,
and West Virginia’’ and the subsequent
supplemental EAs issued in 2013, 2015,
2017, and 2018.
We are making the EA available to the
public for review and comment. We will
consider all comments that we receive
on or before the date listed under the
heading DATES at the beginning of this
VerDate Sep<11>2014
17:47 Jul 08, 2019
Jkt 247001
notice. The EA may be viewed on the
Regulations.gov website or in our
reading room (see ADDRESSES above for
instructions for accessing
Regulations.gov and information on the
location and hours of the reading room).
In addition, paper copies may be
obtained by calling or writing to the
individual listed under FOR FURTHER
INFORMATION CONTACT.
The EA has 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 1b), and (4) APHIS’ NEPA
Implementing Procedures (7 CFR part
372).
Done in Washington, DC, this 2nd day of
July 2019.
Kevin Shea,
Administrator, Animal and Plant Health
Inspection Service.
[FR Doc. 2019–14536 Filed 7–8–19; 8:45 am]
BILLING CODE 3410–34–P
DEPARTMENT OF AGRICULTURE
Animal and Plant Health Inspection
Service
[Docket No. APHIS–2018–0064]
Notice of Availability of an
Environmental Assessment;
Southwestern Willow Flycatcher
Conservation Program
Animal and Plant Health
Inspection Service, USDA.
ACTION: Notice of availability and
request for comments.
AGENCY:
We are advising the public
that the U.S. Department of Agriculture
(USDA) and its sub-agency, the Animal
and Plant Health Inspection Service
(APHIS), are making available a draft
environmental assessment for a
conservation program pursuant to the
Endangered Species Act to benefit the
southwestern willow flycatcher, a small,
neotropical migrant bird found in
Arizona, California, Colorado, Nevada,
New Mexico, Texas, and Utah. The draft
environmental assessment examines the
environmental effects associated with
the selection of the program alternatives
and conservation measures that USDA
and APHIS propose to implement. We
are making the draft environmental
assessment available to the public for
review and comment.
SUMMARY:
PO 00000
Frm 00003
Fmt 4703
Sfmt 4703
32701
We will consider all comments
that we receive on or before August 8,
2019.
ADDRESSES: You may submit comments
by either of the following methods:
• Federal eRulemaking Portal: Go to
https://www.regulations.gov/#!docket
Detail;D=APHIS-2018-0064.
• Postal Mail/Commercial Delivery:
Send your comment to Docket No.
APHIS–2018–0064, Regulatory Analysis
and Development, PPD, APHIS, Station
3A–03.8, 4700 River Road, Unit 118,
Riverdale, MD 20737–1238.
Supporting documents and any
comments we receive on this docket
may be viewed at https://
www.regulations.gov/
#!docketDetail;D=APHIS-2018-0064 or
in our reading room, which 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) 799–7039
before coming.
FOR FURTHER INFORMATION CONTACT: Mr.
Kai Caraher, Biological Scientist, PHP,
PPQ, APHIS, 4700 River Road, Unit 150,
Riverdale, MD 20737–1231; (301) 851–
2345; Kai.Caraher@usda.gov.
SUPPLEMENTARY INFORMATION: Saltcedar,
also known as tamarisk (Tamarix
species), is an invasive plant widely
established in riparian areas in the
western United States. This non-native
weed, which can take the form of a
shrub or small tree, was introduced into
the United States in the latter 19th
century. Although saltcedar is an
invasive plant, native animals have
adapted to its presence.
In 1986, the U.S. Department of
Agriculture’s (USDA’s) Agricultural
Research Service (ARS) began research
into the potential for biological control
of saltcedar. From 1998 to 2000, ARS
conducted open field release trials of
tamarisk leaf beetles (Diorhabda
species) to determine the conditions
under which releases could succeed.
These field trials took place after ARS
consulted with the U.S. Fish and
Wildlife Service (USFWS) to ensure
compliance with the Endangered
Species Act (ESA). USDA’s Animal and
Plant Health Inspection Service (APHIS)
permitted the releases after it completed
additional environmental risk analyses
and provided the public an opportunity
to comment on the documents.
In 2005, APHIS initiated a biological
control program for saltcedar defoliation
in the northern United States using the
tamarisk leaf beetle as the biological
control agent in limited locations
DATES:
E:\FR\FM\09JYN1.SGM
09JYN1
Agencies
[Federal Register Volume 84, Number 131 (Tuesday, July 9, 2019)]
[Notices]
[Pages 32700-32701]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2019-14536]
-----------------------------------------------------------------------
DEPARTMENT OF AGRICULTURE
Animal and Plant Health Inspection Service
[Docket No. APHIS-2019-0034]
Oral Rabies Vaccine Program; Availability of an Environmental
Assessment
AGENCY: Animal and Plant Health Inspection Service, USDA.
ACTION: Notice of availability and request for comments.
-----------------------------------------------------------------------
SUMMARY: We are advising the public that the Animal and Plant Health
Inspection Service has prepared an environmental assessment (EA)
relative to an oral rabies vaccination (ORV) program in Maine, New
Hampshire, New York, Ohio, Tennessee, Texas, Vermont, Virginia, and
West Virginia. The EA analyzes the proposed expanded use of ONRAB
vaccine-baits throughout the ORV distribution zone in those States in
cooperation with the U.S. Forest Service. The proposed expanded ONRAB
vaccine distribution is necessary as a higher level of population
immunity in raccoons is desired in order to maximize the effectiveness
of ORV programs. We are making the EA available to the public for
review and comment.
DATES: We will consider all comments that we receive on or before
August 8, 2019.
ADDRESSES: You may submit comments by either of the following methods:
Federal eRulemaking Portal: Go to https://www.regulations.gov/#!docketDetail;D=APHIS-2019-0034.
Postal Mail/Commercial Delivery: Send your comment to
Docket No. APHIS-2019-0034, Regulatory Analysis and Development, PPD,
APHIS, Station 3A-03.8, 4700 River Road Unit 118, Riverdale, MD 20737-
1238.
The supplemental environmental assessment and any comments we
receive may be viewed at https://www.regulations.gov/#!docketDetail;D=APHIS-2019-0034 or in our reading room, which 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) 799-7039 before coming.
This notice and the supplemental environmental assessment are also
posted on the Animal and Plant Health Inspection Service website at
https://www.aphis.usda.gov/regulations/ws/ws_nepa_environmental_documents.shtml.
FOR FURTHER INFORMATION CONTACT: Mr. Richard Chipman, Rabies Program
Coordinator, Wildlife Services, APHIS, 59 Chennell Drive, Suite 7,
Concord, NH 03301; (603) 223-9623; email: [email protected].
To obtain copies of the supplemental environmental assessment, contact
Ms. Beth Kabert, Staff Wildlife Biologist, Wildlife Services, 59
Chennell Drive, Suite 7, Concord, NH 03301; (908) 442-6761; fax (603)
229-0502; email: [email protected].
SUPPLEMENTARY INFORMATION: The Wildlife Services (WS) program in the
Animal and Plant Health Inspection Service 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 WS addresses.
Wildlife is the dominant reservoir of rabies in the United States.
WS conducts an oral rabies vaccination (ORV) program to control the
spread of rabies. The ORV program has utilized a vaccinia-rabies
glycoprotein (V-RG) vaccine. WS' use of the V-RG vaccine has resulted
in several notable accomplishments, including the elimination of canine
rabies from sources in Mexico, the successful control of gray fox
rabies virus variant in western Texas, and the
[[Page 32701]]
prevention of any appreciable spread of raccoon rabies in the eastern
United States. While the prevention of any appreciable spread of
raccoon rabies in the eastern United States represents a major
accomplishment in rabies management, the V-RG vaccine has not been
effective in eliminating raccoon rabies from high-risk spread
corridors. This fact prompted WS to evaluate rabies vaccines capable of
producing higher levels of population immunity against raccoon rabies
to better control the spread of this disease.
Since 2011, WS has been conducting field trials to study the
immunogenicity and safety of an experimental oral rabies vaccine, a
human adenovirus type 5 rabies glycoprotein recombinant vaccine called
ONRAB (produced by Artemis Technologies Inc., Guelph, Ontario, Canada).
The field trials began in portions of West Virginia, including U.S.
Department of Agriculture Forest Service National Forest System lands.
Beginning in 2012, WS expanded field trials into portions of New
Hampshire, New York, Ohio, Vermont, and new areas of West Virginia,
including National Forest System lands, in order to further assess the
immunogenicity of ONRAB in raccoons and skunks for raccoon rabies virus
variant.
WS is now proposing to further expand ONRAB vaccine distribution to
enhance rabies management in the United States to protect human and
animal health and reduce social costs. The proposed expanded use of
ONRAB is necessary as a higher level of population immunity in raccoons
is desired in order to maximize the effectiveness of ORV programs, and
the RABORAL V-RG vaccine has not produced sufficient levels of
population immunity in skunks (primarily striped skunks) in the wild at
the current dose.
WS has prepared an environmental assessment (EA) in which we
analyze the proposed expanded use of ONRAB vaccine-baits throughout the
ORV distribution zone in Maine, New Hampshire, New York, Ohio,
Tennessee, Texas, Vermont, Virginia, and West Virginia in cooperation
with the U.S. Forest Service. This EA will supersede the 2012 EA
``Field Trial of an Experimental Rabies Vaccine, Human Adenovirus Type
5 Vector in New Hampshire, New York, Ohio, Vermont, and West Virginia''
and the subsequent supplemental EAs issued in 2013, 2015, 2017, and
2018.
We are making the EA available to the public for review and
comment. We will consider all comments that we receive on or before the
date listed under the heading DATES at the beginning of this notice.
The EA may be viewed on the Regulations.gov website or in our reading
room (see ADDRESSES above for instructions for accessing
Regulations.gov and information on the location and hours of the
reading room). In addition, paper copies may be obtained by calling or
writing to the individual listed under FOR FURTHER INFORMATION CONTACT.
The EA has 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 1b), and (4)
APHIS' NEPA Implementing Procedures (7 CFR part 372).
Done in Washington, DC, this 2nd day of July 2019.
Kevin Shea,
Administrator, Animal and Plant Health Inspection Service.
[FR Doc. 2019-14536 Filed 7-8-19; 8:45 am]
BILLING CODE 3410-34-P