Proposed Information Collection; Comment Request; Survey: Expenditures Incurred by Recipients of Biomedical Research and Development Awards From the National Institutes of Health (NIH), 28672-28674 [2014-11453]

Download as PDF 28672 Federal Register / Vol. 79, No. 96 / Monday, May 19, 2014 / Notices SUPPLEMENTARY INFORMATION: Background On October 2, 2013, the Helium Stewardship Act of 2013 (Pub. L. 113– 40) reauthorized the Act. The purpose of the RAC is to improve collaborative relationships among the people that use and care for the National Forests and to provide advice and recommendations to the Forest Service concerning projects and funding consistent with Title II of the Act. The duties of the RAC include monitoring projects, advising the Secretary on the progress and results of the monitoring efforts, and making recommendations to the Forest Service for any appropriate changes or adjustments to the projects being monitored by the RACs. mstockstill on DSK4VPTVN1PROD with NOTICES RAC Membership The RAC will be comprised of 15 members approved by the Secretary of Agriculture. RAC membership will be fairly balanced in terms of the points of view represented and functions to be performed. The RAC members will serve 4-year terms. The RAC shall include representation from the following interest areas: (1) Five persons who represent: (a) Organized Labor or Non-Timber Forest Product Harvester Groups (b) Developed Outdoor Recreation, Off-Highway Vehicle Users, or Commercial Recreation Activities, (c) Energy and Mineral Development, or Commercial or Recreational Fishing Groups, (d) Commercial Timber Industry, or (e) Federal Grazing Permit or Other Land Use Permit Holders, or Representative of Non-Industrial Private Forest Land Owners, within the area for which the committee is organized. (2) Five persons who represent: (a) Nationally or Regionally Recognized Environmental Organizations, (b) Regionally or Locally Recognized Environmental Organizations, (c) Dispersed Recreational Activities, (d) Archaeology and History, or (e) Nationally or Regionally Recognized Wild Horse and Burro Interest, Wildlife Hunting Organizaitons, or Watershed Associations. (3) Five persons who represent: (a) Hold State-Elected Office, (b) Hold County or Local-Elected Office, (c) American Indian Tribes within or adjacent to the area for which the committee is organized, (d) Area School Officials or Teachers, or (e) Affected Public at Large. VerDate Mar<15>2010 17:17 May 16, 2014 Jkt 232001 In the event that a vacancy arises, the Designated Federal Officer may fill the vacancy with a replacement member appointed by the Secretary, if an appropriate replacement member is available. Nominations and Applications Information The appointment of members to the RAC will be made by the Secretary of Agriculture. Any individual or organization may nominate one or more qualified persons to represent the interest areas listed above. To be considered for membership, nominees must: 1. Be a resident of Utah, 2. Identify what interest group they would represent and how they are qualified to represent that interest group, 3. State why they want to serve on the RAC and what they can contribute, 4. Show their past experience in working successfully as part of a working group on forest management activities, and 5. Complete Form AD–755, Advisory Committee or Research and Promotion Background Information. You may contact the person listed above or retrieve the Form AD–755 from the following Web site: www.fs.usda.gov/uwcnf. All nominations will be vetted by the Agency. Equal opportunity practices, in line with the USDA policies, will be followed in all appointments to the RACs. To ensure that the recommendations of the RACs have taken into account the needs of the diverse groups served by the Department, membership should include, to the extent practicable, individuals with demonstrated ability to represent the needs of all racial and ethnic groups, women and men, and persons with disabilities. Dated: May 13, 2014. Gregory Parham, Assistant Secretary of Administration. [FR Doc. 2014–11548 Filed 5–16–14; 8:45 am] BILLING CODE 3410–15–P COMMISSION ON CIVIL RIGHTS Agenda and Notice of Public Meeting of the Massachusetts Advisory Committee Notice is hereby given, pursuant to the provisions of the rules and regulations of the U.S. Commission on Civil Rights (Commission), and the Federal Advisory Committee Act PO 00000 Frm 00002 Fmt 4703 Sfmt 4703 (FACA), that a briefing meeting of the Massachusetts Advisory Committee to the Commission will convene at 10:00 a.m. (EST) on Wednesday, June 11, 2014, at Harvard University Law School, Lewis Hall, 214B, 1557 Massachusetts Avenue, Cambridge, MA 02138. The purpose of the briefing meeting is to hear from government officials, advocates, and other experts on the issue of school discipline in Massachusetts. Members of the public are entitled to submit written comments. The comments must be received in the regional office by Friday, July 11, 2014. Comments may be mailed to the Eastern Regional Office, U.S. Commission on Civil Rights, 1331 Pennsylvania Avenue, Suite 1150, Washington, DC 20425, faxed to (202) 376–7548, or emailed to Melanie Reingardt at ero@usccr.gov. Persons who desire additional information may contact the Eastern Regional Office at 202–376– 7533. Persons needing accessibility services should contact the Eastern Regional Office at least 10 working days before the scheduled date of the meeting. Records generated from this meeting may be inspected and reproduced at the Eastern Regional Office, as they become available, both before and after the meeting. Persons interested in the work of this advisory committee are advised to go to the Commission’s Web site, www.usccr.gov, or to contact the Eastern Regional Office at the above phone number, email, or street address. The meeting will be conducted pursuant to the provisions of the rules and regulations of the Commission and FACA. Dated: May 14, 2014. David Mussatt, Acting Chief, Regional Programs Coordination Unit. [FR Doc. 2014–11503 Filed 5–16–14; 8:45 am] BILLING CODE 6335–01–P DEPARTMENT OF COMMERCE Bureau of Economic Analysis Proposed Information Collection; Comment Request; Survey: Expenditures Incurred by Recipients of Biomedical Research and Development Awards From the National Institutes of Health (NIH) ACTION: Notice. The Department of Commerce, as part of its continuing effort to reduce paperwork and respondent burden, invites the general SUMMARY: E:\FR\FM\19MYN1.SGM 19MYN1 Federal Register / Vol. 79, No. 96 / Monday, May 19, 2014 / Notices mstockstill on DSK4VPTVN1PROD with NOTICES public and other Federal agencies to comment on proposed and/or continuing information collections, as required by the Paperwork Reduction Act of 1995, Public Law 104–13 (44 U.S.C. 3506(c)(2)(A)). DATES: Written comments must be submitted on or before July 18, 2014. ADDRESSES: Direct all written comments to Jennifer Jessup, Departmental Paperwork Clearance Officer, Department of Commerce, Room 6616, 14th and Constitution Avenue NW., Washington, DC 20230, or via email at jjessup@doc.gov. FOR FURTHER INFORMATION CONTACT: Jennifer A. Bennett, Chief, Government Fixed Assets Branch, Government Division (BE–57), Bureau of Economic Analysis, U.S. Department of Commerce, Washington, DC 20230; phone: (202) 606–9769; fax: (202) 606– 5369; or via email at jennifer.bennett@ bea.gov. SUPPLEMENTARY INFORMATION: I. Abstract The survey obtains the distribution of expenditures incurred by recipients of biomedical research awards from the National Institutes of Health (NIH) and will provide information on how the NIH award amounts are expended across several major categories. This information, along with wage and price data from other published sources, will be used to generate the Biomedical Research and Development Price Index (BRDPI). BEA develops this index for NIH under a reimbursable contract. The BRDPI is an index of prices paid for the labor, supplies, equipment, and other inputs required to perform the biomedical research the NIH supports in its intramural laboratories and through its awards to extramural organizations. The BRDPI is a vital tool for planning the NIH research budget and analyzing future NIH programs. A survey of award recipients is currently the only means for updating the expenditure category weights that are used to prepare the BRDPI. The proposed survey change revises the instructions to clarify that respondent’s should report not only expenditures from direct NIH award amounts, but also from NIH awards received as a sub-recipient from another institution. This survey will be voluntary. The authority for NIH to collect information for the BRDPI is provided in 45 CFR subpart C, Post-Award Requirements, § 74.21. This sets forth explicit standards for grantees in establishing and maintaining financial management systems and records, and § 74.53 which VerDate Mar<15>2010 17:17 May 16, 2014 Jkt 232001 provides for the retention of such records as well as NIH access to such records. BEA will administer the survey and analyze the survey results on behalf of NIH, through an interagency agreement between the two agencies. The authority for the NIH to contract with DOC to make this collection is the Economy Act (31 U.S.C. 1535 and 1536). The ‘‘Special Studies’’ authority, 15 U.S.C. 1525 (first paragraph), permits DOC to provide, upon the request of any person, firm, or public or private organization (a) Special studies on matters within the authority of the Department of Commerce, including preparing from its records special compilations, lists, bulletins, or reports, and (b) furnishing transcripts or copies of its studies, compilations and other records. NIH’s support for this research is consistent with the Agency’s duties and authority under 42 U.S.C. 282. The information provided by the respondents will be held confidential and be used for exclusively statistical purposes. This pledge of confidentiality is made under the Confidential Information Protection provisions of title V, subtitle A, Public Law 107–347. Title V is the Confidential Information Protection and Statistical Efficiency Act of 2002 (CIPSEA). Section 512 (on Limitations on Use and Disclosure of Data and Information) of the Act, provides that ‘‘data or information acquired by an agency under a pledge of confidentiality and for exclusively statistical purposes shall be used by officers, employees, or agents of the agency exclusively for statistical purposes. Data or information acquired by an agency under a pledge of confidentiality for exclusively statistical purposes shall not be disclosed by an agency in identifiable form, for any use other than an exclusively statistical purpose, except with the informed consent of the respondent.’’ Responses will be kept confidential and will not be disclosed in identifiable form to anyone, other than employees or agents of BEA or agents of NIH, without prior written permission of the person filing the report. By law, each employee as well as each agent is subject to a jail term of up to 5 years, a fine of up to $250,000, or both for disclosing to the public any identifiable information that is reported about a business or institution. Section 515 of the Information Quality Guidelines applies to this survey. The collection and use of this information complies with all applicable information quality guidelines, i.e., those of the Office of PO 00000 Frm 00003 Fmt 4703 Sfmt 4703 28673 Management and Budget, Department of Commerce, and BEA. II. Method of Collection A survey with a cover letter that includes a brief description of, and rationale for, the survey will be sent by email to potential respondents by the first week of October in 2014 and by August of 2015 and 2016. A report of the respondent’s expenditures of the NIH award amounts, including NIH awards received as a sub-recipient from another institution, following the proposed format for expenditure categories included with the survey form, will be requested to be completed and submitted online no later than December 8, which in most years will be approximately 120 days after mailing. Survey respondents will be selected on the basis of award levels, which determine the weight of the respondent in the biomedical research and development price index. Potential respondents will include (1) The top 100 organizations in total awards, which account for about 73 percent of total awards; (2) 40 additional organizations that are not primarily in the ‘‘Research and Development (R&D) contracts’’ category; and (3) 10 additional organizations that are primarily in the ‘‘R&D contracts’’ category. III. Data OMB Control Number: 0608–0069. Form Number: None. Type of Review: Regular submission. Affected Public: Universities or other organizations that are NIH award recipients. Estimated Number of Respondents: 120. Estimated Time per Response: 16 hours, but may vary among respondents because of differences in institution structure, size, and complexity. Estimated Total Annual Burden Hours: 1,920 hours. Estimated Total Annual Cost to Public: $0. IV. Request for Comments Comments are invited on: (a) Whether the proposed collection of information is necessary for the proper performance of the functions of the NIH, including whether the information has practical utility; (b) the accuracy of the agency’s estimate of the burden (including hours and cost) of the proposed collection of information; (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 respondents, including through the use E:\FR\FM\19MYN1.SGM 19MYN1 28674 Federal Register / Vol. 79, No. 96 / Monday, May 19, 2014 / Notices of automated collection techniques or other forms of information technology. Comments submitted in response to this notice will be summarized and/or included in the request for OMB approval of this information collection; they also will become a matter of public record. Dated: May 13, 2014. Glenna Mickelson, Management Analyst, Office of Chief Information Officer. [FR Doc. 2014–11453 Filed 5–16–14; 8:45 am] BILLING CODE 3510–EA–P DEPARTMENT OF COMMERCE Foreign-Trade Zones Board [B–3–2014] Foreign-Trade Zone 49—Newark, New Jersey Area; Authorization of Production Activity; Western Carriers, Inc. (Kitting of Liquor Gift Sets), North Bergen, New Jersey On January 13, 2014, the Port Authority of New York and New Jersey, grantee of FTZ 49, submitted a notification of proposed production activity to the Foreign-Trade Zones (FTZ) Board on behalf of Western Carriers, Inc., within FTZ 49—Site 15, in North Bergen, New Jersey. The notification was processed in accordance with the regulations of the FTZ Board (15 CFR part 400), including notice in the Federal Register inviting public comment (79 FR 4442, 1–28–2014). The FTZ Board has determined that no further review of the activity is warranted at this time. The production activity described in the notification is authorized, subject to the FTZ Act and the FTZ Board’s regulations, including Section 400.14. Dated: May 13, 2014, Andrew McGilvray, Executive Secretary. [FR Doc. 2014–11529 Filed 5–16–14; 8:45 am] BILLING CODE 3510–DS–P DEPARTMENT OF COMMERCE International Trade Administration mstockstill on DSK4VPTVN1PROD with NOTICES [A–570–014] 53-Foot Domestic Dry Containers From the People’s Republic of China: Initiation of Antidumping Duty Investigation Enforcement and Compliance, International Trade Administration, Department of Commerce. DATES: Effective Date: May 19, 2014. AGENCY: VerDate Mar<15>2010 17:17 May 16, 2014 Jkt 232001 John Drury and Brian Davis, Office VI, AD/ CVD Operations, Enforcement and Compliance, International Trade Administration, U.S. Department of Commerce, 14th Street and Constitution Avenue NW., Washington, DC 20230; telephone: (202) 482–0195 and (202) 482–7924, respectively. SUPPLEMENTARY INFORMATION: FOR FURTHER INFORMATION CONTACT: The Petition On April 23, 2014, the Department of Commerce (Department) received an antidumping duty (AD) petition concerning imports of 53-foot domestic dry containers (domestic dry containers) from the People’s Republic of China (PRC), officially filed in proper form on behalf of a U.S. producer of domestic dry containers, Stoughton Trailers, LLC (Petitioner).1 The AD Petition was accompanied by a countervailing duty (CVD) petition concerning imports of domestic dry containers from the PRC. On April 25, 2014, and May 6, 2014, the Department requested additional information and clarification of certain areas of the Petition, and on April 30, 2014, and May 8, 2014, respectively, Petitioner filed responses to these requests.2 In accordance with section 732(b) of the Tariff Act of 1930, as amended (the Act), Petitioner alleges that imports of domestic dry containers from the PRC are being, or are likely to be, sold in the United States at less than fair value within the meaning of section 731 of the Act, and that such imports materially retard the establishment of an industry in the United States, or in the alternative, that the U.S. industry is materially injured or threatened with material injury by reason of such imports. Also, consistent with section 732(b)(1) of the Act, the Petition is accompanied by information reasonably available to Petitioner in support of its allegations. The Department finds that Petitioner filed the Petition on behalf of the domestic industry because Petitioner is 1 See ‘‘Petition for the Imposition of Antidumping Duties on Imports of 53-Foot Domestic Dry Containers from the People’s Republic of China,’’ dated April 23, 2014 (hereafter referred to as the ‘‘Petition’’). 2 See Petitioner’s, filing titled, ‘‘Response to Department of Commerce Supplemental Questions, Volume II: Sales at Less Than Normal Value,’’ dated April 30, 2014 (AD Supplement); see also ‘‘Response to Department of Commerce Supplemental Questions, Volume I: General Issues,’’ dated April 30, 2014 (General Issues Supplement); and ‘‘Petition for the Imposition of Antidumping and Countervailing Duties, Supplemental Submission, Petition Volume II: 53Foot Domestic Dry Containers from the People’s Republic of China’’, dated May 8, 2014 (AD Supplement 2). PO 00000 Frm 00004 Fmt 4703 Sfmt 4703 an interested party as defined in section 771(9)(C) of the Act, and that Petitioner demonstrated sufficient industry support with respect to the initiation of the AD investigation that Petitioner is requesting.3 Period of Investigation The period of investigation (POI) is October 1, 2013, through March 31, 2014. Scope of the Investigation The product covered by this investigation is domestic dry containers from the PRC. For a full description of the scope of the investigation, please see the ‘‘Scope of the Investigation’’ in Appendix I of this notice. Comments on the Scope of the Investigation During our review of the Petition, the Department issued questions to, and received responses from, Petitioner pertaining to the proposed scope language in order to ensure that such language is an accurate reflection of the product for which the domestic industry is seeking relief.4 As discussed in the preamble to the Department’s regulations,5 we are setting aside a period for interested parties to raise issues regarding product coverage. The period of scope comments is intended to provide the Department with ample opportunity to consider all comments and to consult with parties prior to the issuance of the preliminary determination. All comments must be filed by 5:00 p.m. Eastern Daylight Time (EDT) on June 2, 2014, which is twenty calendar days from the signature date of this notice. Any rebuttal comments must be filed by 5:00 p.m. EDT on June 9, 2014. All such comments must be filed on the records of the AD investigation, as well as the concurrent CVD investigation. Filing Requirements All comments and submissions to the Department must be filed electronically using Enforcement and Compliance’s Antidumping and Countervailing Duty Centralized Electronic Service System (IA ACCESS). An electronically filed document must be received successfully in its entirety by the time and date of the applicable deadline noted above. Documents excepted from the electronic submission requirements must be filed 3 See ‘‘Determination of Industry Support for the Petition’’ section, below. 4 See General Issues Supplemental Questions, dated April 25, 2014; see also General Issues Supplement, at 1–2 and Exhibit SG–2. 5 See Antidumping Duties; Countervailing Duties; Final Rule, 62 FR 27296, 27323 (May 19, 1997). E:\FR\FM\19MYN1.SGM 19MYN1

Agencies

[Federal Register Volume 79, Number 96 (Monday, May 19, 2014)]
[Notices]
[Pages 28672-28674]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2014-11453]


=======================================================================
-----------------------------------------------------------------------

DEPARTMENT OF COMMERCE

Bureau of Economic Analysis


Proposed Information Collection; Comment Request; Survey: 
Expenditures Incurred by Recipients of Biomedical Research and 
Development Awards From the National Institutes of Health (NIH)

ACTION: Notice.

-----------------------------------------------------------------------

SUMMARY: The Department of Commerce, as part of its continuing effort 
to reduce paperwork and respondent burden, invites the general

[[Page 28673]]

public and other Federal agencies to comment on proposed and/or 
continuing information collections, as required by the Paperwork 
Reduction Act of 1995, Public Law 104-13 (44 U.S.C. 3506(c)(2)(A)).

DATES: Written comments must be submitted on or before July 18, 2014.

ADDRESSES: Direct all written comments to Jennifer Jessup, Departmental 
Paperwork Clearance Officer, Department of Commerce, Room 6616, 14th 
and Constitution Avenue NW., Washington, DC 20230, or via email at 
jjessup@doc.gov.

FOR FURTHER INFORMATION CONTACT: Jennifer A. Bennett, Chief, Government 
Fixed Assets Branch, Government Division (BE-57), Bureau of Economic 
Analysis, U.S. Department of Commerce, Washington, DC 20230; phone: 
(202) 606-9769; fax: (202) 606-5369; or via email at 
jennifer.bennett@bea.gov.

SUPPLEMENTARY INFORMATION:

I. Abstract

    The survey obtains the distribution of expenditures incurred by 
recipients of biomedical research awards from the National Institutes 
of Health (NIH) and will provide information on how the NIH award 
amounts are expended across several major categories. This information, 
along with wage and price data from other published sources, will be 
used to generate the Biomedical Research and Development Price Index 
(BRDPI). BEA develops this index for NIH under a reimbursable contract. 
The BRDPI is an index of prices paid for the labor, supplies, 
equipment, and other inputs required to perform the biomedical research 
the NIH supports in its intramural laboratories and through its awards 
to extramural organizations. The BRDPI is a vital tool for planning the 
NIH research budget and analyzing future NIH programs. A survey of 
award recipients is currently the only means for updating the 
expenditure category weights that are used to prepare the BRDPI.
    The proposed survey change revises the instructions to clarify that 
respondent's should report not only expenditures from direct NIH award 
amounts, but also from NIH awards received as a sub-recipient from 
another institution.
    This survey will be voluntary. The authority for NIH to collect 
information for the BRDPI is provided in 45 CFR subpart C, Post-Award 
Requirements, Sec.  74.21. This sets forth explicit standards for 
grantees in establishing and maintaining financial management systems 
and records, and Sec.  74.53 which provides for the retention of such 
records as well as NIH access to such records.
    BEA will administer the survey and analyze the survey results on 
behalf of NIH, through an interagency agreement between the two 
agencies. The authority for the NIH to contract with DOC to make this 
collection is the Economy Act (31 U.S.C. 1535 and 1536).
    The ``Special Studies'' authority, 15 U.S.C. 1525 (first 
paragraph), permits DOC to provide, upon the request of any person, 
firm, or public or private organization (a) Special studies on matters 
within the authority of the Department of Commerce, including preparing 
from its records special compilations, lists, bulletins, or reports, 
and (b) furnishing transcripts or copies of its studies, compilations 
and other records. NIH's support for this research is consistent with 
the Agency's duties and authority under 42 U.S.C. 282.
    The information provided by the respondents will be held 
confidential and be used for exclusively statistical purposes. This 
pledge of confidentiality is made under the Confidential Information 
Protection provisions of title V, subtitle A, Public Law 107-347. Title 
V is the Confidential Information Protection and Statistical Efficiency 
Act of 2002 (CIPSEA). Section 512 (on Limitations on Use and Disclosure 
of Data and Information) of the Act, provides that ``data or 
information acquired by an agency under a pledge of confidentiality and 
for exclusively statistical purposes shall be used by officers, 
employees, or agents of the agency exclusively for statistical 
purposes. Data or information acquired by an agency under a pledge of 
confidentiality for exclusively statistical purposes shall not be 
disclosed by an agency in identifiable form, for any use other than an 
exclusively statistical purpose, except with the informed consent of 
the respondent.''
    Responses will be kept confidential and will not be disclosed in 
identifiable form to anyone, other than employees or agents of BEA or 
agents of NIH, without prior written permission of the person filing 
the report. By law, each employee as well as each agent is subject to a 
jail term of up to 5 years, a fine of up to $250,000, or both for 
disclosing to the public any identifiable information that is reported 
about a business or institution.
    Section 515 of the Information Quality Guidelines applies to this 
survey. The collection and use of this information complies with all 
applicable information quality guidelines, i.e., those of the Office of 
Management and Budget, Department of Commerce, and BEA.

II. Method of Collection

    A survey with a cover letter that includes a brief description of, 
and rationale for, the survey will be sent by email to potential 
respondents by the first week of October in 2014 and by August of 2015 
and 2016. A report of the respondent's expenditures of the NIH award 
amounts, including NIH awards received as a sub-recipient from another 
institution, following the proposed format for expenditure categories 
included with the survey form, will be requested to be completed and 
submitted online no later than December 8, which in most years will be 
approximately 120 days after mailing. Survey respondents will be 
selected on the basis of award levels, which determine the weight of 
the respondent in the biomedical research and development price index. 
Potential respondents will include (1) The top 100 organizations in 
total awards, which account for about 73 percent of total awards; (2) 
40 additional organizations that are not primarily in the ``Research 
and Development (R&D) contracts'' category; and (3) 10 additional 
organizations that are primarily in the ``R&D contracts'' category.

III. Data

    OMB Control Number: 0608-0069.
    Form Number: None.
    Type of Review: Regular submission.
    Affected Public: Universities or other organizations that are NIH 
award recipients.
    Estimated Number of Respondents: 120.
    Estimated Time per Response: 16 hours, but may vary among 
respondents because of differences in institution structure, size, and 
complexity.
    Estimated Total Annual Burden Hours: 1,920 hours.
    Estimated Total Annual Cost to Public: $0.

IV. Request for Comments

    Comments are invited on: (a) Whether the proposed collection of 
information is necessary for the proper performance of the functions of 
the NIH, including whether the information has practical utility; (b) 
the accuracy of the agency's estimate of the burden (including hours 
and cost) of the proposed collection of information; (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 respondents, including through the use

[[Page 28674]]

of automated collection techniques or other forms of information 
technology.
    Comments submitted in response to this notice will be summarized 
and/or included in the request for OMB approval of this information 
collection; they also will become a matter of public record.

    Dated: May 13, 2014.
Glenna Mickelson,
Management Analyst, Office of Chief Information Officer.
[FR Doc. 2014-11453 Filed 5-16-14; 8:45 am]
BILLING CODE 3510-EA-P
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