60 day FRN

Federal Register / Vol. 82, No. 27 / Friday, February 10, 2017 / Notices
Notice: Section 309(a) of the Clean Air
Act requires that EPA make public its
comments on EISs issued by other
Federal agencies. EPA’s comment letters
on EISs are available at: http://
www.epa.gov/compliance/nepa/
eisdata.html.
EIS No. 20170023, Draft Supplement,
DOS, MN, Line 67 Expansion
(previously known as the Alberta
Clipper Pipeline), Comment Period
Ends: 03/27/2017, Contact: Mary D.
Hassell 202–736–7428.
EIS No. 20170024, Revised Final, USFS,
SC, Francis Marion Forest Plan
Revision, Review Period Ends: 03/13/
2017, Contact: Mary Morrison 803–
561–4058.
Amended Notices
EIS No. 20160311, Draft, USACE, NE.,
Missouri River Recovery Management
Plan, Comment Period Ends: 04/24/
2017, Contact: Aaron Quinn 402–995–
2669, Revision to FR Notice Published
12/23/2016; Extending Comment
Period from 2/24/2017 to 4/24/2017.
Dated: February 7, 2017.
Dawn Roberts,
Management Analyst, NEPA Compliance
Division, Office of Federal Activities.
[FR Doc. 2017–02805 Filed 2–9–17; 8:45 am]
BILLING CODE 6560–50–P

FEDERAL MARITIME COMMISSION
Sunshine Act Meeting
Federal
Maritime Commission.
TIME AND DATE: February 15, 2017; 10:00
a.m.
PLACE: 800 N. Capitol Street NW., First
Floor Hearing Room, Washington, DC.
STATUS: The meeting will be held in
Open Session and will be streamed live
at http://fmc.capitolconnection.org/.
MATTERS TO BE CONSIDERED:
AGENCY HOLDING THE MEETING:

Open Session

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1. Briefing by Commissioner Doyle on
the Competition Law in the
Transport Sector Conference
2. Staff Update on Docket No. 16–05:
Service Contracts and NVOCC
Service Arrangements
CONTACT PERSON FOR MORE INFORMATION:

Rachel E. Dickon, Assistant Secretary,
(202) 523 5725.

FEDERAL RESERVE SYSTEM
Formations of, Acquisitions by, and
Mergers of Bank Holding Companies
The companies listed in this notice
have applied to the Board for approval,
pursuant to the Bank Holding Company
Act of 1956 (12 U.S.C. 1841 et seq.)
(BHC Act), Regulation Y (12 CFR part
225), and all other applicable statutes
and regulations to become a bank
holding company and/or to acquire the
assets or the ownership of, control of, or
the power to vote shares of a bank or
bank holding company and all of the
banks and nonbanking companies
owned by the bank holding company,
including the companies listed below.
The applications listed below, as well
as other related filings required by the
Board, are available for immediate
inspection at the Federal Reserve Bank
indicated. The applications will also be
available for inspection at the offices of
the Board of Governors. Interested
persons may express their views in
writing on the standards enumerated in
the BHC Act (12 U.S.C. 1842(c)). If the
proposal also involves the acquisition of
a nonbanking company, the review also
includes whether the acquisition of the
nonbanking company complies with the
standards in section 4 of the BHC Act
(12 U.S.C. 1843). Unless otherwise
noted, nonbanking activities will be
conducted throughout the United States.
Unless otherwise noted, comments
regarding each of these applications
must be received at the Reserve Bank
indicated or the offices of the Board of
Governors not later than March 9, 2017.
A. Federal Reserve Bank of St. Louis
(David L. Hubbard, Senior Manager)
P.O. Box 442, St. Louis, Missouri
63166–2034. Comments can also be sent
electronically to
[email protected]:
1. Tyronza Bancshares, Inc., Marked
Tree, Arkansas; to indirectly acquire
6.25 percent of the voting shares of
Pinnacle Bancshares, Inc., and thereby
indirectly acquire Pinnacle Bank, both
of Rogers, Arkansas.
Board of Governors of the Federal Reserve
System, February 7, 2017.
Yao-Chin Chao,
Assistant Secretary of the Board.
[FR Doc. 2017–02800 Filed 2–9–17; 8:45 am]
BILLING CODE P

Rachel E. Dickon,
Assistant Secretary.
[FR Doc. 2017–02881 Filed 2–8–17; 4:15 pm]
BILLING CODE 6731–AA–P

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10357

DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60Day–17–17OB: Docket No. ATSDR–2017–
0002]

Proposed Data Collection Submitted
for Public Comment and
Recommendations
Agency for Toxic Substances
and Disease Registry (ATSDR),
Department of Health and Human
Services (HHS).
ACTION: Notice with comment period.
AGENCY:

Agency for Toxic Substances
and Disease Registry (ATSDR), as part of
its continuing efforts to reduce public
burden and maximize the utility of
government information, invites the
general public and other Federal
agencies to take this opportunity to
comment on proposed and/or
continuing information collections, as
required by the Paperwork Reduction
Act of 1995. This notice invites
comment on a proposed information
collection project titled
‘‘Characterization of Exposure Potential
during Activities Conducted on
Synthetic Turf with Crumb Rubber
Infill.’’ The purpose of the proposed
study is to evaluate and characterize
human exposure potential to
constituents in crumb rubber infill.
DATES: Written comments must be
received on or before April 11, 2017.
ADDRESSES: You may submit comments,
identified by Docket No. ATSDR–2017–
0002 by any of the following methods:
• Federal eRulemaking Portal:
Regulations.gov. Follow the instructions
for submitting comments.
• Mail: Leroy A. Richardson,
Information Collection Review Office,
Centers for Disease Control and
Prevention, 1600 Clifton Road NE., MS–
D74, Atlanta, Georgia 30329.
Instructions: All submissions received
must include the agency name and
Docket Number. All relevant comments
received will be posted without change
to Regulations.gov, including any
personal information provided. For
access to the docket to read background
documents or comments received, go to
Regulations.gov.
Please note: All public comment
should be submitted through the
Federal eRulemaking portal
(Regulations.gov) or by U.S. mail to the
address listed above.
FOR FURTHER INFORMATION CONTACT: To
request more information on the
proposed project or to obtain a copy of
SUMMARY:

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Federal Register / Vol. 82, No. 27 / Friday, February 10, 2017 / Notices

the information collection plan and
instruments, contact the Information
Collection Review Office, Centers for
Disease Control and Prevention, 1600
Clifton Road NE., MS–D74, Atlanta,
Georgia 30329; phone: 404–639–7570;
Email: [email protected].
SUPPLEMENTARY INFORMATION: Under the
Paperwork Reduction Act of 1995 (PRA)
(44 U.S.C. 3501–3520), Federal agencies
must obtain approval from the Office of
Management and Budget (OMB) for each
collection of information they conduct
or sponsor. In addition, the PRA also
requires Federal agencies to provide a
60-day notice in the Federal Register
concerning each proposed collection of
information, including each new
proposed collection, each proposed
extension of existing collection of
information, and each reinstatement of
previously approved information
collection before submitting the
collection to OMB for approval. To
comply with this requirement, we are
publishing this notice of a proposed
data collection as described below.
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 shall have
practical utility; (b) the accuracy of the
agency’s estimate of the burden of the
proposed collection of information; (c)
ways to enhance the quality, utility, and
clarity of the information to be
collected; (d) ways to minimize the
burden of the collection of information
on respondents, including through the
use of automated collection techniques
or other forms of information
technology; and (e) estimates of capital
or start-up costs and costs of operation,
maintenance, and purchase of services
to provide information. Burden means
the total time, effort, or financial
resources expended by persons to
generate, maintain, retain, disclose or
provide information to or for a Federal
agency. This includes the time needed
to review instructions; to develop,
acquire, install and utilize technology
and systems for the purpose of
collecting, validating and verifying
information, processing and
maintaining information, and disclosing
and providing information; to train
personnel and to be able to respond to
a collection of information, to search
data sources, to complete and review
the collection of information; and to
transmit or otherwise disclose the
information.

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Proposed Project
Characterization of Exposure Potential
during Activities Conducted on
Synthetic Turf with Crumb Rubber
Infill—New—Agency for Toxic
Substances and Disease Registry
(ATSDR).
Background and Brief Description
Currently in the United States, there
are more than 12,000 synthetic turf
fields in use. While the Synthetic Turf
Council has set guidelines for the
content of crumb rubber used as infill in
synthetic turf fields, manufacturing
processes result in differences among
types of crumb rubber. Additionally, the
chemical composition may vary highly
between different processes and source
materials and may vary even within
granules from the same origin.
In July, 2016, the Agency for Toxic
Substances and Disease Registry
(ATSDR) and the United States
Environmental Protection Agency
(USEPA) were granted an emergency
Paperwork Reduction Act (PRA)
clearance for a research study titled
‘‘Collections Related to Synthetic Turf
Fields with Crumb Rubber Infill’’ (OMB
Control No. 0923–0054, expiration date
01/31/2017). The research goals for the
three activities in the protocol are pilotlevel investigations to evaluate and
characterize: (1) The chemical
composition and use of crumb rubber
infill in synthetic turf using a
convenience sample of nine tire
recycling manufacturing plants and 40
facilities that use synthetic turf fields
(Activity 1); (2) the human exposure
potential to constituents in crumb
rubber infill among a convenience
sample of 60 field users (Activity 2); and
(3) collection of biological specimens
(blood and urine) from 45 participants
from Activity 2 (Activity 3).
By December, 2016, ATSDR and
USEPA completed Activity 1 which was
aimed at characterizing the chemical
composition and use of synthetic turf
fields with tire crumb rubber infill. The
agencies successfully consented and
sampled 40 synthetic turf fields with
crumb rubber infill across the United
States. The activities are reported in the
‘‘Status Report on the Federal Research
Action Plan on Recycled Tire Crumb
Used on Playing Fields and
Playgrounds.’’ The Status Report was
released on December 30, 2016.
During Activity 1, ATSDR and USEPA
obtained permission to return to
participating fields to complete the
human exposure characterization. Due

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to the limited time constraints and field
activity schedules, ATSDR and USEPA
chose to begin Activity 2 data collection
and Activity 3 specimen collection in
2017.
The agencies are requesting a new
information collection request (ICR) for
a two-year OMB clearance to complete
Activity 2 and Activity 3, now subtitled
‘‘Characterization of Exposure Potential
during Activities Conducted on
Synthetic Turf with Crumb Rubber
Infill.’’ This will be the first assessment
of activities conducted on synthetic turf
for the purpose of characterizing
potential exposure patterns. The study
will include persons who use synthetic
turf with crumb rubber infill (e.g.,
facility users) and who routinely
perform activities that would result in a
high level of contact to crumb rubber.
This will allow for evaluation of
potential high-end exposures to
constituents in synthetic turf among this
group of users. The respondents will be
administered a detailed questionnaire
on activity patterns on synthetic turf
with crumb rubber infill. This
instrument, along with extant
videography of persons engaged in
activities of interest (see below), will be
used to characterize exposure scenarios,
including the nature and duration of
potential exposures.
Additionally, we will conduct an
exposure characterization sub-study
among a subset of the respondents. We
will use a subset of the facilities
sampled in the first study to conduct
activities for the exposure
characterization of facility users. The
exposure characterization sub-study
will include field environment
sampling, personal air monitoring,
dermal sampling, and urine and blood
collection. Video data collection of
facility user activities will be performed
for a subset of respondents. It is likely
that some of the collection items will
not be analyzed in the current project
time frame but will be archived for
future analysis.
The research study will screen a total
of 75 participants for eligibility. The
sample size for the exposure
characterization study is 60 respondents
and 45 respondents for the exposure
measurements sub-study. The total
burden hours for the research study is
174 hours among all of the 75
respondents. There is no cost to the
respondents other than their time in the
study.

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Federal Register / Vol. 82, No. 27 / Friday, February 10, 2017 / Notices
ESTIMATED ANNUALIZED BURDEN HOURS
Average
burden per
response
(in hours)

Total burden
(in hours)

Form name

Adult/Adolescent Field Users ......

Eligibility Screening Script ......................
Adult and Adolescent Questionnaire .....
Exposure Measurement Form ...............
Phlebotomist Safety Exclusion Questions Form.
Eligibility Screening Script ......................

41
36
27
27

1
1
1
1

5/60
30/60
3
2/60

4
18
81
1

34

1

5/60

3

24
18

1
1

30/60
2/60

12
1

Youth/Child Field Users ..............

Youth and Child Questionnaire ..............
Phlebotomist Safety Exclusion Questions Form.
Exposure Measurement Form ...............

18

1

3

54

Total .....................................

.................................................................

........................

........................

........................

174

Parents/Guardians of Youth/Child
Field Users.

Leroy A. Richardson,
Chief, Information Collection Review Office,
Office of Scientific Integrity, Office of the
Associate Director for Science, Office of the
Director, Centers for Disease Control and
Prevention.
[FR Doc. 2017–02760 Filed 2–9–17; 8:45 am]
BILLING CODE 4163–18–P

DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60Day–17–17ND; Docket No. CDC–2017–
0007]

Proposed Data Collection Submitted
for Public Comment and
Recommendations
Centers for Disease Control and
Prevention (CDC), Department of Health
and Human Services (HHS).
ACTION: Notice with comment period.
AGENCY:

The Centers for Disease
Control and Prevention (CDC), as part of
its continuing efforts to reduce public
burden and maximize the utility of
government information, invites the
general public and other Federal
agencies to take this opportunity to
comment on proposed and/or
continuing information collections, as
required by the Paperwork Reduction
Act of 1995. This notice invites
comment on a proposed information
collection entitled ‘‘Grants for Injury
Control Research Centers Annual
Progress Report (APR).’’ CDC will
collect information from grantees
funded under Grants for Injury Control
and Research Centers (ICRC) for the
Annual Progress Report (APR). The APR
is used to monitor the ICRCs’ progress
on set performance indicators, activities,

SUMMARY:

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Number of
responses per
respondent

Number of
respondents

Type of respondents

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and progress towards stated grant
objectives.
DATES: Written comments must be
received on or before April 11, 2017.
ADDRESSES: You may submit comments,
identified by Docket No. CDC–2017–
0007 by any of the following methods:
• Federal eRulemaking Portal:
Regulations.gov. Follow the instructions
for submitting comments.
• Mail: Leroy A. Richardson,
Information Collection Review Office,
Centers for Disease Control and
Prevention, 1600 Clifton Road NE., MS–
D74, Atlanta, Georgia 30329.
Instructions: All submissions received
must include the agency name and
Docket Number. All relevant comments
received will be posted without change
to Regulations.gov, including any
personal information provided. For
access to the docket to read background
documents or comments received, go to
Regulations.gov.
Please note: All public comment should be
submitted through the Federal eRulemaking
portal (Regulations.gov) or by U.S. mail to the
address listed above.

To
request more information on the
proposed project or to obtain a copy of
the information collection plan and
instruments, contact the Information
Collection Review Office, Centers for
Disease Control and Prevention, 1600
Clifton Road NE., MS–D74, Atlanta,
Georgia 30329; phone: 404–639–7570;
Email: [email protected].
SUPPLEMENTARY INFORMATION: Under the
Paperwork Reduction Act of 1995 (PRA)
(44 U.S.C. 3501–3520), Federal agencies
must obtain approval from the Office of
Management and Budget (OMB) for each
collection of information they conduct
or sponsor. In addition, the PRA also
requires Federal agencies to provide a
60-day notice in the Federal Register
FOR FURTHER INFORMATION CONTACT:

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concerning each proposed collection of
information, including each new
proposed collection, each proposed
extension of existing collection of
information, and each reinstatement of
previously approved information
collection before submitting the
collection to OMB for approval. To
comply with this requirement, we are
publishing this notice of a proposed
data collection as described below.
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 shall have
practical utility; (b) the accuracy of the
agency’s estimate of the burden of the
proposed collection of information; (c)
ways to enhance the quality, utility, and
clarity of the information to be
collected; (d) ways to minimize the
burden of the collection of information
on respondents, including through the
use of automated collection techniques
or other forms of information
technology; and (e) estimates of capital
or start-up costs and costs of operation,
maintenance, and purchase of services
to provide information. Burden means
the total time, effort, or financial
resources expended by persons to
generate, maintain, retain, disclose or
provide information to or for a Federal
agency. This includes the time needed
to review instructions; to develop,
acquire, install and utilize technology
and systems for the purpose of
collecting, validating and verifying
information, processing and
maintaining information, and disclosing
and providing information; to train
personnel and to be able to respond to
a collection of information, to search
data sources, to complete and review
the collection of information; and to
transmit or otherwise disclose the
information.

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