Agency Information Collection Activities: Submission for the Office of Management and Budget (OMB) Review; Comment Request, 63441-63442 [2014-25252]
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Federal Register / Vol. 79, No. 205 / Thursday, October 23, 2014 / Notices
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common analysis is potent and can
greatly inform studies on the feeding
behavior of whales in the region. The
applicants would use standard dartbiopsy methods that have been used for
more than 2 decades and are proven to
be both humane and appropriate. A
small sterilized stainless steel tip would
be attached to the end of a customized
crossbow bolt that has a flotation
stopper engineered on to it. When the
dart hits the whale, it penetrates the
outermost skin and collects a ∼10×5 mm
sample of both skin and blubber. These
samples are placed in sterilized
cryovials and kept in ¥20 °C freezers
until they are shipped frozen back to the
labs for analysis. For satellite tagging,
they are testing specific hypotheses
regarding how the movement and
behavior of humpback whales relates to
that of their prey, Antarctic krill, and
sea ice in the Antarctic environment.
Satellite-transmitting tags offer the
opportunity to track the movement of
individual whales over long time
periods and in relation to physical
processes in their environment. They
will deploy 10 satellite-linked
implantable tags, designed to a
maximum of 290mm into the back of the
whale (generally just forward and to the
left or right side of the dorsal fin). The
tag is designed to penetrate just beneath
the skin and hypodermis to anchor the
tag. All external components of the tag
are built from stainless steel and the tag
is surgically sterilized prior to
deployment. Each tag is deployed with
the use of a compressed air gun. Once
deployed, each tag turns on during the
subsequent dive of the whale. Tags will
then transmit upon each initial
surfacing, and each 30 seconds of
subsequent ‘dry time’ until the tag falls
off the whale, malfunctions or the single
AA lithium battery is exhausted.
Investigators with significant experience
in these methods would conduct both
biopsy and satellite tagging.
Location: Antarctic Peninsula
between Marguerite Bay and the
Gerlache Strait, inshore waters.
Dates: January 1, 2015–December 31,
2018.
Nadene G. Kennedy,
Polar Coordination Specialist, Division of
Polar Programs.
[FR Doc. 2014–25235 Filed 10–22–14; 8:45 am]
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NATIONAL SCIENCE FOUNDATION
NUCLEAR REGULATORY
COMMISSION
Advisory Committee for International
Science and Engineering; Notice of
Meeting
[Docket No. NRC–2014–0155]
In accordance with Federal Advisory
Committee Act (Pub., L. 92–463, as
amended), the National Science
Foundation announces the following
meeting:
Name: Advisory Committee for
International Science and Engineering
Meeting. #25104.
Date/Time: November 6, 2014: 11 a.m.
to 2 p.m.
Place: National Science Foundation,
4121 Wilson Boulevard, Stafford II—
Suite 1155, Arlington, Virginia 22230.
Type of Meeting: OPEN, VIRTUAL.
Contact Person: Diane Drew, National
Science Foundation, 4201 Wilson
Boulevard, Arlington, Virginia 22230
703–292–7220.
Minutes: Meeting minutes and other
information may be obtained from the
AC–ISE Designated Federal Official at
the above address or the Web site at
https://www.nsf.gov/od/iia/ise/
advisory.jsp.
Purpose of Meeting: To provide
advice and recommendations on major
goals and policies pertaining to
International programs and activities.
Agenda
Thursday, November 6, 2014 11 a.m.–2
p.m.
• Welcome and Opening Remarks
• Update on the Status of the ISE
Section
• Presentation and Discussion of the
Report from the ISE Committee of
Visitors
• Presentation and Discussion of the
Strategic Framework for International
Engagement
• Discussion of Other Recent
Evaluations of NSF International
Activities
• (Tentative) Meeting with France
´
Cordova, NSF Director
• Closing Remarks and Wrap Up
Dated: October 17, 2014.
Suzanne Plimpton,
Acting Committee Management Officer.
[FR Doc. 2014–25153 Filed 10–22–14; 8:45 am]
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Agency Information Collection
Activities: Submission for the Office of
Management and Budget (OMB)
Review; Comment Request
Nuclear Regulatory
Commission.
ACTION: Notice of the OMB review of
information collection and solicitation
of public comment.
AGENCY:
The U.S. Nuclear Regulatory
Commission (NRC) has recently
submitted to OMB for review the
following proposal for the collection of
information under the provisions of the
Paperwork Reduction Act of 1995 (44
U.S.C. Chapter 35). The NRC hereby
informs potential respondents that an
agency may not conduct or sponsor, and
that a person is not required to respond
to, a collection of information unless it
displays a currently valid OMB control
number. The NRC published a Federal
Register notice with a 60-day comment
period on this information collection on
July 2, 2014.
1. Type of submission, new, revision,
or extension: Extension.
2. The title of the information
collection: NRC Form 483, ‘‘Registration
Certificate—In Vitro Testing with
Byproduct Material Under General
License.’’
3. Current OMB approval number:
3150–0038.
4. How often the collection is
required: There is a one-time submittal
of information to receive a validated
copy of NRC Form 483 with an assigned
registration number. In addition, any
changes in the information reported on
NRC Form 483 must be reported in
writing to the NRC within 30 days after
the effective date of such change.
5. Who will be required or asked to
report: Any physician, veterinarian in
the practice of veterinary medicine,
clinical laboratory or hospital which
desires a general license to receive,
acquire, possess, transfer, or use
specified units of byproduct material in
certain in vitro clinical or laboratory
tests.
6. An estimate of the number of
annual responses: 8 responses.
7. The estimated number of annual
respondents: 8 respondents.
8. An estimate of the total number of
hours needed annually to complete the
requirement or request: 1.18 hours (1.07
hours reporting + 0.11 hour
recordkeeping).
9. Abstract: Section 31.11 of Title 10
of the Code of Federal Regulations (10
SUMMARY:
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Federal Register / Vol. 79, No. 205 / Thursday, October 23, 2014 / Notices
CFR), establishes a general license
authorizing any physician, clinical
laboratory, veterinarian in the practice
of veterinary medicine, or hospital to
possess certain small quantities of
byproduct material for in vitro clinical
or laboratory test not involving the
internal or external administration of
the byproduct material or the radiation
therefrom to human beings or animals.
Possession of byproduct material under
10 CFR 31.11 is not authorized until the
physician, clinical laboratory,
veterinarian in the practice of veterinary
medicine, or hospital has filed NRC
Form 483 and received from the
Commission a validated copy of NRC
Form 483 with a registration number.
The public may examine and have
copied for a fee publicly-available
documents, including the final
supporting statement, at the NRC’s
Public Document Room, Room O–1F21,
One White Flint North, 11555 Rockville
Pike, Rockville, Maryland 20852. The
OMB clearance requests are available at
the NRC’s Web site: https://www.nrc.gov/
public-involve/doc-comment/omb/. The
document will be available on the
NRC’s home page site for 60 days after
the signature date of this notice.
Comments and questions should be
directed to the OMB reviewer listed
below by November 24, 2014.
Comments received after this date will
be considered if it is practical to do so,
but assurance of consideration cannot
be given to comments received after this
date. Vlad Dorjets, Desk Officer, Office
of Information and Regulatory Affairs
(3150–0038), NEOB–10202, Office of
Management and Budget, Washington,
DC 20503.
Comments can also be emailed to
Vladik_Dorjets@omb.eop.gov or
submitted by telephone at 202–395–
7315.
The NRC Clearance Officer is
Tremaine Donnell, telephone: 301–415–
6258.
mstockstill on DSK4VPTVN1PROD with NOTICES
Dated at Rockville, Maryland, this 20th day
of October 2014.
For the Nuclear Regulatory Commission.
Tremaine Donnell,
NRC Clearance Officer, Office of Information
Services.
[FR Doc. 2014–25252 Filed 10–22–14; 8:45 am]
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NUCLEAR REGULATORY
COMMISSION
[Docket No. 70–3098; NRC–2014–0235]
Shaw AREVA MOX Services; Mixed
Oxide Fuel Fabrication Facility
Nuclear Regulatory
Commission.
ACTION: Environmental assessment and
finding of no significant impact;
issuance.
AGENCY:
The U.S. Nuclear Regulatory
Commission (NRC) is considering
extending the expiration date for
Construction Authorization (CA)
CAMOX–001 issued to Shaw AREVA
MOX Services for the Mixed Oxide Fuel
Fabrication Facility on the Savannah
River Site in Aiken, South Carolina.
ADDRESSES: Please refer to Docket ID
NRC–2014–0235 when contacting the
NRC about the availability of
information regarding this document.
You may obtain publicly-available
information related to this action by the
following methods:
• Federal Rulemaking Web site: Go to
https://www.regulations.gov and search
for Docket ID NRC–2014–0235. Address
questions about NRC dockets to Carol
Gallagher; telephone: 301–287–3422;
email: Carol.Gallagher@nrc.gov. For
technical questions, contact the
individual listed in the FOR FURTHER
INFORMATION CONTACT section of this
document.
• NRC’s Agencywide Documents
Access and Management System
(ADAMS): You may obtain publiclyavailable documents online in the NRC
Library at https://www.nrc.gov/readingrm/adams.html. To begin the search,
select ‘‘ADAMS Public Documents’’ and
then select ‘‘Begin Web-based ADAMS
Search.’’ For problems with ADAMS,
please contact the NRC’s Public
Document Room (PDR) reference staff at
1–800–397–4209, 301–415–4737, or by
email to pdr.resource@nrc.gov. The
ADAMS accession number for each
document referenced in this notice (if
that document is available in ADAMS)
is provided the first time that a
document is referenced. The request to
extend the construction authorization
expiration date, dated May 16, 2014, is
available in ADAMS under Accession
No. ML14132A342.
• NRC’s PDR: You may examine and
purchase copies of public documents at
the NRC’s PDR, Room O1–F21, One
White Flint North, 11555 Rockville
Pike, Rockville, Maryland 20852.
FOR FURTHER INFORMATION CONTACT:
David Tiktinsky, Office of Nuclear
Material Safety and Safeguards, U.S.
SUMMARY:
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Nuclear Regulatory Commission;
Washington, DC 20555–0001; telephone:
301–287–9155; email: David.Tiktinsky@
nrc.gov.
SUPPLEMENTARY INFORMATION:
I. Introduction
The NRC is considering extending the
CA expiration date specified in CA
CAMOX–001 issued to Shaw AREVA
MOX Services (MOX Services) for the
Mixed Oxide Fuel Fabrication Facility.
The facility is located on the
Department of Energy’s Savannah River
Site in Aiken, South Carolina.
Therefore, as required by § 51.21 of Title
10 of the Code of Federal Regulations
(10 CFR), the NRC performed an
environmental assessment. Based on the
results of the environmental assessment
that follows, the NRC has determined
not to prepare an environmental impact
statement for the action of extending the
expiration date of the construction
authorization, and is issuing a finding of
no significant impact.
II. Environmental Assessment
Identification of the Proposed Action
The proposed action would extend
the expiration date of CA CAMOX–001
from March 30, 2015, to March 30, 2025.
MOX Services submitted the CA
extension request by letter dated May
12, 2014 (ADAMS Accession No.
ML14132A342). MOX Services
submitted the request to extend the CA
at least 90 days before the expiration of
the existing CA, therefore, in accordance
with 10 CFR 2.109(a), the existing CA
will remain in effect until the NRC staff
has completed the review of the request.
The proposed extension will not
expand the scope of any work to be
performed that is not already allowed by
the existing construction authorization.
The extension will grant the MOX
Services additional time to complete
construction in accordance with the
previously approved CA.
The Need for the Proposed Action
The proposed action is necessary to
give the CA holder adequate time to
complete construction of the Mixed
Oxide Fuel Fabrication Facility. The CA
for the MFFF was originally issued on
March 30, 2005, with an expiration date
of March 31, 2015. MOX Services has
stated in their May 12, 2014, request
that various factors have contributed to
the need for an extension of the CA. The
factors include: (a) The MFFF is a
unique first of a kind facility of this type
to be licensed in the United States
under 10 CFR part 70; (b) annual
funding/appropriations supporting
construction activities have been less
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Agencies
[Federal Register Volume 79, Number 205 (Thursday, October 23, 2014)]
[Notices]
[Pages 63441-63442]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2014-25252]
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NUCLEAR REGULATORY COMMISSION
[Docket No. NRC-2014-0155]
Agency Information Collection Activities: Submission for the
Office of Management and Budget (OMB) Review; Comment Request
AGENCY: Nuclear Regulatory Commission.
ACTION: Notice of the OMB review of information collection and
solicitation of public comment.
-----------------------------------------------------------------------
SUMMARY: The U.S. Nuclear Regulatory Commission (NRC) has recently
submitted to OMB for review the following proposal for the collection
of information under the provisions of the Paperwork Reduction Act of
1995 (44 U.S.C. Chapter 35). The NRC hereby informs potential
respondents that an agency may not conduct or sponsor, and that a
person is not required to respond to, a collection of information
unless it displays a currently valid OMB control number. The NRC
published a Federal Register notice with a 60-day comment period on
this information collection on July 2, 2014.
1. Type of submission, new, revision, or extension: Extension.
2. The title of the information collection: NRC Form 483,
``Registration Certificate--In Vitro Testing with Byproduct Material
Under General License.''
3. Current OMB approval number: 3150-0038.
4. How often the collection is required: There is a one-time
submittal of information to receive a validated copy of NRC Form 483
with an assigned registration number. In addition, any changes in the
information reported on NRC Form 483 must be reported in writing to the
NRC within 30 days after the effective date of such change.
5. Who will be required or asked to report: Any physician,
veterinarian in the practice of veterinary medicine, clinical
laboratory or hospital which desires a general license to receive,
acquire, possess, transfer, or use specified units of byproduct
material in certain in vitro clinical or laboratory tests.
6. An estimate of the number of annual responses: 8 responses.
7. The estimated number of annual respondents: 8 respondents.
8. An estimate of the total number of hours needed annually to
complete the requirement or request: 1.18 hours (1.07 hours reporting +
0.11 hour recordkeeping).
9. Abstract: Section 31.11 of Title 10 of the Code of Federal
Regulations (10
[[Page 63442]]
CFR), establishes a general license authorizing any physician, clinical
laboratory, veterinarian in the practice of veterinary medicine, or
hospital to possess certain small quantities of byproduct material for
in vitro clinical or laboratory test not involving the internal or
external administration of the byproduct material or the radiation
therefrom to human beings or animals. Possession of byproduct material
under 10 CFR 31.11 is not authorized until the physician, clinical
laboratory, veterinarian in the practice of veterinary medicine, or
hospital has filed NRC Form 483 and received from the Commission a
validated copy of NRC Form 483 with a registration number.
The public may examine and have copied for a fee publicly-available
documents, including the final supporting statement, at the NRC's
Public Document Room, Room O-1F21, One White Flint North, 11555
Rockville Pike, Rockville, Maryland 20852. The OMB clearance requests
are available at the NRC's Web site: https://www.nrc.gov/public-involve/doc-comment/omb/. The document will be available on the NRC's home page
site for 60 days after the signature date of this notice.
Comments and questions should be directed to the OMB reviewer
listed below by November 24, 2014. Comments received after this date
will be considered if it is practical to do so, but assurance of
consideration cannot be given to comments received after this date.
Vlad Dorjets, Desk Officer, Office of Information and Regulatory
Affairs (3150-0038), NEOB-10202, Office of Management and Budget,
Washington, DC 20503.
Comments can also be emailed to Vladik_Dorjets@omb.eop.gov or
submitted by telephone at 202-395-7315.
The NRC Clearance Officer is Tremaine Donnell, telephone: 301-415-
6258.
Dated at Rockville, Maryland, this 20th day of October 2014.
For the Nuclear Regulatory Commission.
Tremaine Donnell,
NRC Clearance Officer, Office of Information Services.
[FR Doc. 2014-25252 Filed 10-22-14; 8:45 am]
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