Notice of Availability of an Environmental Assessment for the Release of Aphalara Itadori for the Biological Control of Japanese, Giant, and Bohemian Knotweeds, 37825-37826 [2019-16581]
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Notices
Federal Register
Vol. 84, No. 149
Friday, August 2, 2019
This section of the FEDERAL REGISTER
contains documents other than rules or
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DEPARTMENT OF AGRICULTURE
Submission for OMB Review;
Comment Request
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July 30, 2019.
The Department of Agriculture has
submitted the following information
collection requirement(s) to OMB for
review and clearance under the
Paperwork Reduction Act of 1995,
Public Law 104–13. Comments are
requested regarding; whether the
collection of information is necessary
for the proper performance of the
functions of the agency, including
whether the information will have
practical utility; the accuracy of the
agency’s estimate of burden including
the validity of the methodology and
assumptions used; ways to enhance the
quality, utility and clarity of the
information to be collected; ways to
minimize the burden of the collection of
information on those who are to
respond, including through the use of
appropriate automated, electronic,
mechanical, or other technological
collection techniques or other forms of
information technology.
Comments regarding this information
collection received by September 3,
2019 will be considered. Written
comments should be addressed to: Desk
Officer for Agriculture, Office of
Information and Regulatory Affairs,
Office of Management and Budget
(OMB), New Executive Office Building,
725 17th Street NW, Washington, DC
20502. Commenters are encouraged to
submit their comments to OMB via
email to: OIRA_Submission@
OMB.EOP.GOV or fax (202) 395–5806
and to Departmental Clearance Office,
USDA, OCIO, Mail Stop 7602,
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the submission(s) may be obtained by
calling (202) 720–8958.
An agency may not conduct or
sponsor a collection of information
unless the collection of information
displays a currently valid OMB control
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number and the agency informs
potential persons who are to respond to
the collection of information that such
person are not required to respond to
the collection of information unless it
displays a currently valid OMB control
number.
Office of the Chief Financial Officer
Title: Supplier Credit Audit Recovery.
OMB Control Number: 0505–0026.
Summary of Collection: On March 10,
2010, the President signed a presidential
memorandum directing all federal
departments and agencies to expand
and intensify their use of payment
recapture audits. These are audits which
offer specialized private auditors
financial incentives to root out improper
payments, and have been demonstrated
through pilot programs to be highly
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Budget’s Circular A123 Appendix C
(2018), offers guidance to implement the
requirements of the Improper Payments
Elimination and Recovery Act of 2010,
which requires agencies to conduct
payment recapture audits for each
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collection can be found under the
Improper Payments Elimination and
Recovery Act of 2010 (124 Statute 2229,
Pub. L. 111–204), under Section C,
Recovery Audit Contracts.
Need and Use of the Information: The
Office of the Chief Financial Officer
(OCFO) sends out a letter to USDA
vendors on an annual basis requesting
account and payment information as to
whether the vendor currently has a
credit on their books due back to USDA.
If the information is not collected,
OCFO would not be able to identify the
root cause of improper payments and
would not be able to accomplishment
this without verification of suspected
overpayments to suppliers or vendors.
Description of Respondents: Business
or other for-profit.
Number of Respondents: 10,514.
Frequency of Responses: Third party
disclosure; Reporting: Semi-annually.
Total Burden Hours: 21,028.
Ruth Brown,
Departmental Information Collection
Clearance Officer.
[FR Doc. 2019–16494 Filed 8–1–19; 8:45 am]
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DEPARTMENT OF AGRICULTURE
Animal and Plant Health Inspection
Service
[Docket No. APHIS–2019–0002]
Notice of Availability of an
Environmental Assessment for the
Release of Aphalara Itadori for the
Biological Control of Japanese, Giant,
and Bohemian Knotweeds
Animal and Plant Health
Inspection Service, USDA.
ACTION: Notice of availability; reopening
of comment period.
AGENCY:
We are reopening the
comment period for an environmental
assessment relative to permitting the
release of Aphalara itadori for the
biological control of Japanese, Giant,
and Bohemian knotweeds (Fallopia
japonica, F. sachalinensis, and F. x
bohemica), significant invasive weeds,
within the contiguous United States.
This action will allow interested
persons additional time to prepare and
submit comments.
DATES: The comment period for the
notice published on May 28, 2019 (84
FR 24463) is reopened. We will consider
all comments that we receive on or
before August 26, 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-2019-0002.
• Postal Mail/Commercial Delivery:
Send your comment to Docket No.
APHIS–2019–0002, 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-2019-0002 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) 7997039 before coming.
FOR FURTHER INFORMATION CONTACT: Dr.
Colin D. Stewart, Assistant Director,
Pests, Pathogens, and Biocontrol
Permits, Permitting and Compliance
SUMMARY:
E:\FR\FM\02AUN1.SGM
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37826
Federal Register / Vol. 84, No. 149 / Friday, August 2, 2019 / Notices
Coordination, PPQ, APHIS, 4700 River
Road Unit 133, Riverdale, MD 20737–
1231; (301) 851–2237; email:
Colin.Stewart@usda.gov.
SUPPLEMENTARY INFORMATION: On May
28, 2019, we published in the Federal
Register (84 FR 24463, Docket No.
APHIS–2019–0002) a notice of
availability for an environmental
assessment relative to permitting the
release of Aphalara itadori for the
biological control of Japanese, Giant,
and Bohemian knotweeds (Fallopia
japonica, F. sachalinensis, and F. x
bohemica), significant invasive weeds,
within the contiguous United States.
Comments on the notice were
required to be received on or before June
27, 2019. We are reopening the
comment period on Docket No. APHIS–
2019–0002 for an additional 60 days.
This action will allow interested
persons additional time to prepare and
submit comments.
We will also consider all comments
received between June 28, 2019 (the day
after the close of the original comment
period) and the date of this notice.
Done in Washington, DC, this 30th day of
July 2019.
Kevin Shea,
Administrator, Animal and Plant Health
Inspection Service.
[FR Doc. 2019–16581 Filed 8–1–19; 8:45 am]
BILLING CODE 3410–34–P
DEPARTMENT OF AGRICULTURE
Animal and Plant Health Inspection
Service
[Docket No. APHIS–2019–0043]
Availability of an Environmental
Assessment for Field Testing of a
Pseudogymnoascus destructans
Vaccine, Live Raccoon Poxvirus
Vector (RCN–CAL/SP)
Animal and Plant Health
Inspection Service, USDA.
ACTION: Notice.
AGENCY:
We are advising the public
that the Animal and Plant Health
Inspection Service has prepared an
environmental assessment concerning
authorization to ship for the purpose of
field testing, and then to field test, an
unlicensed Pseudogymnoascus
destructans Vaccine, Live Raccoon
Poxvirus Vector (RCN–CAL/SP). The
environmental assessment, which is
based on a risk analysis prepared to
assess the risks associated with the field
testing of this vaccine, examines the
potential effects that field testing this
veterinary vaccine could have on the
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SUMMARY:
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quality of the human environment.
Based on the risk analysis, we have
reached a preliminary determination
that field testing this veterinary vaccine
will not have a significant impact on the
quality of the human environment, and
that an environmental impact statement
need not be prepared. We intend to
authorize shipment of this vaccine for
field testing following the close of the
comment period for this notice unless
new substantial issues bearing on the
effects of this action are brought to our
attention. We also intend to issue a U.S.
Veterinary Biological Product license for
this vaccine, provided the field test data
support the conclusions of the
environmental assessment and the
issuance of a finding of no significant
impact and the product meets all other
requirements for licensing.
DATES: We will consider all comments
that we receive on or before September
3, 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-2019-0043.
• Postal Mail/Commercial Delivery:
Send your comment to Docket No.
APHIS–2019–0043, 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-2019-0043 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) 7997039 before coming.
FOR FURTHER INFORMATION CONTACT: Dr.
Barbara J. Sheppard, Senior Staff
Veterinary Medical Officer, Center for
Veterinary Biologics, Policy, Evaluation,
and Licensing, VS, APHIS, 1920 Dayton
Avenue, Ames, IA 50010; phone (515)
337–6100; fax (515) 337–6120.
For information regarding the
environmental assessment or the risk
analysis, or to request a copy of the
environmental assessment (as well as
the risk analysis with confidential
business information removed), contact
Dr. Mathew Erdman, Senior Staff
Veterinary Medical Officer, Center for
Veterinary Biologics, Policy, Evaluation,
and Licensing VS, APHIS, 1920 Dayton
Avenue, P.O. Box 844, Ames, IA 50010;
phone (515) 337–6100, fax (515) 337–
6120.
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Under the
Virus-Serum-Toxin Act (21 U.S.C. 151
et seq.), a veterinary biological product
must be shown to be pure, safe, potent,
and efficacious before a veterinary
biological product license may be
issued. A field test is generally
necessary to satisfy prelicensing
requirements for veterinary biological
products. Prior to conducting a field test
on an unlicensed product, an applicant
must obtain approval from the Animal
and Plant Health Inspection Service
(APHIS), as well as obtain APHIS’
authorization to ship the product for
field testing.
To determine whether to authorize
shipment and grant approval for the
field testing of the unlicensed product
referenced in this notice, APHIS
conducted a risk analysis to assess the
potential effects of this product on the
safety of animals, public health, and the
environment. Based on the risk analysis,
APHIS has prepared an environmental
assessment (EA) concerning the field
testing of the following unlicensed
veterinary biological product:
Requester: U.S. Geological Survey,
National Wildlife Health Center.
Product: Pseudogymnoascus
destructans Vaccine, Live Raccoon
Poxvirus Vector (RCN–CAL/SP).
Possible Field Test Locations:
Colorado, Iowa, Minnesota, Nebraska,
Oklahoma, Texas, or Wisconsin, among
others.
The above-mentioned product
consists of a live recombinant raccoon
poxvirus vector expressing two
Pseudogymnoascus destructans
proteins. The vaccine is for the oral
vaccination of bats as an aid in the
prevention and control of White-Nose
Syndrome.
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).
Unless substantial issues with adverse
environmental impacts are raised in
response to this notice, APHIS intends
to issue a finding of no significant
impact (FONSI) based on the EA and
authorize shipment of the above product
for the initiation of field tests following
the close of the comment period for this
notice.
Because the issues raised by field
testing and by issuance of a license are
identical, APHIS has concluded that the
SUPPLEMENTARY INFORMATION:
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Agencies
[Federal Register Volume 84, Number 149 (Friday, August 2, 2019)]
[Notices]
[Pages 37825-37826]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2019-16581]
-----------------------------------------------------------------------
DEPARTMENT OF AGRICULTURE
Animal and Plant Health Inspection Service
[Docket No. APHIS-2019-0002]
Notice of Availability of an Environmental Assessment for the
Release of Aphalara Itadori for the Biological Control of Japanese,
Giant, and Bohemian Knotweeds
AGENCY: Animal and Plant Health Inspection Service, USDA.
ACTION: Notice of availability; reopening of comment period.
-----------------------------------------------------------------------
SUMMARY: We are reopening the comment period for an environmental
assessment relative to permitting the release of Aphalara itadori for
the biological control of Japanese, Giant, and Bohemian knotweeds
(Fallopia japonica, F. sachalinensis, and F. x bohemica), significant
invasive weeds, within the contiguous United States. This action will
allow interested persons additional time to prepare and submit
comments.
DATES: The comment period for the notice published on May 28, 2019 (84
FR 24463) is reopened. We will consider all comments that we receive on
or before August 26, 2019.
ADDRESSES: You may submit comments by either of the following methods:
Federal eRulemaking Portal: Go to https://www.regulations.gov/#!docketDetail;D=APHIS-2019-0002.
Postal Mail/Commercial Delivery: Send your comment to
Docket No. APHIS-2019-0002, 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-2019-
0002 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) 7997039 before coming.
FOR FURTHER INFORMATION CONTACT: Dr. Colin D. Stewart, Assistant
Director, Pests, Pathogens, and Biocontrol Permits, Permitting and
Compliance
[[Page 37826]]
Coordination, PPQ, APHIS, 4700 River Road Unit 133, Riverdale, MD
20737-1231; (301) 851-2237; email: [email protected].
SUPPLEMENTARY INFORMATION: On May 28, 2019, we published in the
Federal Register (84 FR 24463, Docket No. APHIS-2019-0002) a notice of
availability for an environmental assessment relative to permitting the
release of Aphalara itadori for the biological control of Japanese,
Giant, and Bohemian knotweeds (Fallopia japonica, F. sachalinensis, and
F. x bohemica), significant invasive weeds, within the contiguous
United States.
Comments on the notice were required to be received on or before
June 27, 2019. We are reopening the comment period on Docket No. APHIS-
2019-0002 for an additional 60 days. This action will allow interested
persons additional time to prepare and submit comments.
We will also consider all comments received between June 28, 2019
(the day after the close of the original comment period) and the date
of this notice.
Done in Washington, DC, this 30th day of July 2019.
Kevin Shea,
Administrator, Animal and Plant Health Inspection Service.
[FR Doc. 2019-16581 Filed 8-1-19; 8:45 am]
BILLING CODE 3410-34-P