Registration Review; Draft Human Health and/or Ecological Risk Assessments for Benfluralin, Bromuconazole, Carbaryl, Clodinafop-propargyl, Deltamethrin, Diflufenzopyr, Esfenvalerate, Lufenuron, and Mepiquat Chloride/Mepiquat Pentaborate; Notice of Availability, 36135-36136 [2017-16372]

Download as PDF Federal Register / Vol. 82, No. 148 / Thursday, August 3, 2017 / Notices ENVIRONMENTAL PROTECTION AGENCY [EPA–HQ–OPP–2017–0011; FRL–9961–84] Registration Review; Draft Human Health and/or Ecological Risk Assessments for Benfluralin, Bromuconazole, Carbaryl, Clodinafoppropargyl, Deltamethrin, Diflufenzopyr, Esfenvalerate, Lufenuron, and Mepiquat Chloride/Mepiquat Pentaborate; Notice of Availability Environmental Protection Agency (EPA). ACTION: Notice. AGENCY: This notice announces the availability of EPA’s draft risk human health and/or ecological risk assessments for the registration review of benfluralin, bromuconazole, carbaryl, clodinafop-propargyl, deltamethrin, diflufenzopyr, esfenvalerate, lufenuron, and mepiquat chloride/mepiquat pentaborate. Registration review is EPA’s periodic review of pesticide registrations to ensure that each pesticide continues to satisfy the statutory standard for registration, that is, the pesticide can perform its intended function without unreasonable adverse effects on human health or the environment. As part of the registration review process, the Agency has completed a comprehensive draft human health and/or ecological risk assessments for all pesticides listed in the Table in Unit III. After reviewing comments received during the public comment period, EPA will issue revised risk assessments, explain any changes to the draft risk assessments, and respond to comments and may request public input on risk mitigation before completing proposed registration review decisions for the pesticides listed in the Table in Unit III. Through this program, EPA is ensuring that each pesticide’s registration is based on current scientific and other knowledge, including its effects on human health and the environment. DATES: Comments must be received on or before October 2, 2017. ADDRESSES: Submit your comments, identified by docket identification (ID) number EPA–HQ–OPP–2015–0794, by one of the following methods: • Federal eRulemaking Portal: https:// www.regulations.gov. Follow the online instructions for submitting comments. Do not submit electronically any information you consider to be Confidential Business Information (CBI) or other information whose disclosure is restricted by statute. mstockstill on DSK30JT082PROD with NOTICES SUMMARY: VerDate Sep<11>2014 16:35 Aug 02, 2017 Jkt 241001 • Mail: OPP Docket, Environmental Protection Agency Docket Center (EPA/ DC), (28221T), 1200 Pennsylvania Ave. NW., Washington, DC 20460–0001. • Hand Delivery: To make special arrangements for hand delivery or delivery of boxed information, please follow the instructions at https:// www.epa.gov/dockets/contacts.html. Additional instructions on commenting or visiting the docket, along with more information about dockets generally, is available at https:// www.epa.gov/dockets. FOR FURTHER INFORMATION CONTACT: For pesticide specific information contact: The Chemical Review Manager identified for the pesticide of interest in the Table in Unit III. For general questions on the registration review program, contact: Dana Friedman, Pesticide Re-Evaluation Division (7508P), Office of Pesticide Programs, Environmental Protection Agency, 1200 Pennsylvania Ave. NW., Washington, DC 20460–0001; telephone number: (703) 347–8827; email address: friedman.dana@epa.gov. SUPPLEMENTARY INFORMATION: I. General Information A. Does this action apply to me? This action is directed to the public in general, and may be of interest to a wide range of stakeholders including environmental, human health, farm worker, and agricultural advocates; the chemical industry; pesticide users; and members of the public interested in the sale, distribution, or use of pesticides. Since others also may be interested, the Agency has not attempted to describe all the specific entities that may be affected by this action. If you have any questions regarding the applicability of this action to a particular entity, consult the Chemical Review Manager identified for the pesticide of interest in the Table in Unit III. B. What should I consider as I prepare my comments for EPA? 1. Submitting CBI. Do not submit this information to EPA through regulations.gov or email. Clearly mark the part or all of the information that you claim to be CBI. For CBI information in a disk or CD–ROM that you mail to EPA, mark the outside of the disk or CD–ROM as CBI and then identify electronically within the disk or CD–ROM the specific information that is claimed as CBI. In addition to one complete version of the comment that includes information claimed as CBI, a copy of the comment that does not contain the information claimed as CBI PO 00000 Frm 00022 Fmt 4703 Sfmt 4703 36135 must be submitted for inclusion in the public docket. Information so marked will not be disclosed except in accordance with procedures set forth in 40 CFR part 2. 2. Tips for preparing your comments. When preparing and submitting your comments, see the commenting tips at https://www.epa.gov/dockets/ comments.html. 3. Environmental justice. EPA seeks to achieve environmental justice, the fair treatment and meaningful involvement of any group, including minority and/or low income populations, in the development, implementation, and enforcement of environmental laws, regulations, and policies. To help address potential environmental justice issues, the Agency seeks information on any groups or segments of the population who, as a result of their location, cultural practices, or other factors, may have atypical or disproportionately high and adverse human health impacts or environmental effects from exposure to the pesticides discussed in this document, compared to the general population. II. Authority EPA is conducting its registration review of the pesticides listed in the Table in Unit III pursuant to section 3(g) of the Federal Insecticide, Fungicide, and Rodenticide Act (FIFRA) and the Procedural Regulations for Registration Review at 40 CFR part 155, subpart C. Section 3(g) of FIFRA provides, among other things, that the registrations of pesticides are to be reviewed every 15 years. Under FIFRA, a pesticide product may be registered or remain registered only if it meets the statutory standard for registration given in FIFRA section 3(c)(5) (7 U.S.C. 136a(c)(5)). When used in accordance with widespread and commonly recognized practice, the pesticide product must perform its intended function without unreasonable adverse effects on the environment; that is, without any unreasonable risk to man or the environment, or a human dietary risk from residues that result from the use of a pesticide in or on food. III. Registration Reviews As directed by FIFRA section 3(g), EPA is reviewing the pesticide registrations for the pesticides listed in the Table of this unit to ensure that they continue to satisfy the FIFRA standard for registration—that is, that these pesticides can still be used without unreasonable adverse effects on human health or the environment. E:\FR\FM\03AUN1.SGM 03AUN1 36136 Federal Register / Vol. 82, No. 148 / Thursday, August 3, 2017 / Notices TABLE—DRAFT RISK ASSESSMENTS BEING MADE AVAILABLE FOR PUBLIC COMMENT Pesticide Docket ID No. Benfluralin, Case 2030 ....................... Bromuconazole, Case 7035 ............... Carbaryl, Case 0080 .......................... Clodinafop-propargyl, Case 7250 ...... Deltamethrin, Case 7414 ................... Diflufenzopyr, Case 7246 ................... Esfenvalerate, Case 7406 .................. Lufenuron, Case 7627 ....................... Mepiquat Chloride/Mepiquat Pentaborate, Case 2375. mstockstill on DSK30JT082PROD with NOTICES Registration review case name and No. EPA–HQ–OPP–2011–0931 EPA–HQ–OPP–2015–0535 EPA–HQ–OPP–2010–0230 EPA–HQ–OPP–2012–0424 EPA–HQ–OPP–2009–0637 EPA–HQ–OPP–2011–0911 EPA–HQ–OPP–2009–0301 EPA–HQ–OPP–2015–0098 EPA–HQ–OPP–2012–0083 Pursuant to 40 CFR 155.53(c), EPA is providing an opportunity, through this notice of availability, for interested parties to provide comments and input concerning the Agency’s draft human health and/or ecological risk assessments for the pesticides listed in the Table in Unit III. Such comments and input could address, among other things, the Agency’s risk assessment methodologies and assumptions, as applied to these draft risk assessments. The Agency will consider all comments received during the public comment period and make changes, as appropriate, to the draft human health and/or ecological risk assessments. EPA will then issue revised risk assessments, explain any changes to the draft risk assessments, and respond to comments. In the Federal Register notice announcing the availability of the revised risk assessments, if the revised risk assessment indicates risks of concern, the Agency may provide a comment period for the public to submit suggestions for mitigating the risk identified in the revised risk assessment before developing proposed registration review decisions for the pesticides listed in the Table in Unit III. 1. Information submission requirements. Anyone may submit data or information in response to this document. To be considered during a pesticide’s registration review, the submitted data or information must meet the following requirements: • To ensure that EPA will consider data or information submitted, interested persons must submit the data or information during the comment period. The Agency may, at its discretion, consider data or information submitted at a later date. • The data or information submitted must be presented in a legible and useable form. For example, an English translation must accompany any material that is not in English and a written transcript must accompany any information submitted as an audiographic or videographic record. VerDate Sep<11>2014 16:35 Aug 02, 2017 Jkt 241001 Chemical Review Manager,telephone number, email address Brian Kettl, kettl.brian@epa.gov, (703) 347–0535. Thomas Harty, harty.thomas@epa.gov, (703) 347–0338. Linsey Walsh, walsh.linsey@epa.gov, (703) 347–8030. Wilhelmena Livingston, livingston.wilhelmena@epa.gov, (703) 308–8025. Bilin Basu, basu.bilin@epa.gov, (703) 347–0455. Bilin Basu, basu.bilin@epa.gov, (703) 347–0455. Marianne Mannix, mannix.marianne@epa.gov, (703) 347–0275. Bonnie Adler, adler.bonnie@epa.gov, (703) 308–8523. Caitlin Newcamp, newcamp.caitlin@epa.gov, (703) 347–0325. Written material may be submitted in paper or electronic form. • Submitters must clearly identify the source of any submitted data or information. • Submitters may request the Agency to reconsider data or information that the Agency rejected in a previous review. However, submitters must explain why they believe the Agency should reconsider the data or information in the pesticide’s registration review. As provided in 40 CFR 155.58, the registration review docket for each pesticide case will remain publicly accessible through the duration of the registration review process; that is, until all actions required in the final decision on the registration review case have been completed. Authority: 7 U.S.C. 136 et seq. Dated: May 11, 2017. Yu-Ting Guilaran, Director, Pesticide Re-Evaluation Division, Office of Pesticide Programs. [FR Doc. 2017–16372 Filed 8–2–17; 8:45 am] BILLING CODE 6560–50–P ENVIRONMENTAL PROTECTION AGENCY [EPA–HQ–OPP–2016–0618; FRL–9963–97] Cancellation Order for Certain Pesticide Registrations and/or Amendments To Terminate Uses; Correction Environmental Protection Agency (EPA). ACTION: Notice; correction. AGENCY: EPA issued a notice in the Federal Register of November 22, 2016, concerning receipt of requests to voluntarily cancel certain pesticide registrations and/or amend registrations to terminate certain uses. EPA also issued a notice in the Federal Register of April 10, 2017, concerning cancellation of certain pesticide SUMMARY: PO 00000 Frm 00023 Fmt 4703 Sfmt 4703 registrations and/or amendments to terminate uses. This document corrects a typographical error in both of these notices. The EPA registration number for one of the products being voluntarily cancelled was listed incorrectly in the original notices. FOR FURTHER INFORMATION CONTACT: Christina Scheltema, Pesticide Reevaluation Division (7508P), Office of Pesticide Programs, Environmental Protection Agency, 1200 Pennsylvania Ave. NW., Washington, DC 20460–0001; telephone number: (703) 308–2201; email address: scheltema.christina@ epa.gov. SUPPLEMENTARY INFORMATION: I. General Information A. Does this action apply to me? The Agency included in both the November 22, 2016 and April 10, 2017 notices a list of those who may be potentially affected by this action. B. How can I get copies of this document and other related information? The docket for this action, identified by docket identification (ID) number EPA–HQ–OPP–2016–0618, is available at https://www.regulations.gov or at the Office of Pesticide Programs Regulatory Public Docket (OPP Docket) in the Environmental Protection Agency Docket Center (EPA/DC), West William Jefferson Clinton Bldg., Rm. 3334, 1301 Constitution Ave. NW., Washington, DC 20460–0001. The Public Reading Room is open from 8:30 a.m. to 4:30 p.m., Monday through Friday, excluding legal holidays. The telephone number for the Public Reading Room is (202) 566–1744, and the telephone number for the OPP Docket is (703) 305–5805. Please review the visitor instructions and additional information about the docket available at https://www.epa.gov/dockets. II. What does this correction do? The EPA registration number for one of the products being voluntarily cancelled was listed incorrectly in the E:\FR\FM\03AUN1.SGM 03AUN1

Agencies

[Federal Register Volume 82, Number 148 (Thursday, August 3, 2017)]
[Notices]
[Pages 36135-36136]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2017-16372]



[[Page 36135]]

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ENVIRONMENTAL PROTECTION AGENCY

[EPA-HQ-OPP-2017-0011; FRL-9961-84]


Registration Review; Draft Human Health and/or Ecological Risk 
Assessments for Benfluralin, Bromuconazole, Carbaryl, Clodinafop-
propargyl, Deltamethrin, Diflufenzopyr, Esfenvalerate, Lufenuron, and 
Mepiquat Chloride/Mepiquat Pentaborate; Notice of Availability

AGENCY: Environmental Protection Agency (EPA).

ACTION: Notice.

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

SUMMARY: This notice announces the availability of EPA's draft risk 
human health and/or ecological risk assessments for the registration 
review of benfluralin, bromuconazole, carbaryl, clodinafop-propargyl, 
deltamethrin, diflufenzopyr, esfenvalerate, lufenuron, and mepiquat 
chloride/mepiquat pentaborate. Registration review is EPA's periodic 
review of pesticide registrations to ensure that each pesticide 
continues to satisfy the statutory standard for registration, that is, 
the pesticide can perform its intended function without unreasonable 
adverse effects on human health or the environment. As part of the 
registration review process, the Agency has completed a comprehensive 
draft human health and/or ecological risk assessments for all 
pesticides listed in the Table in Unit III. After reviewing comments 
received during the public comment period, EPA will issue revised risk 
assessments, explain any changes to the draft risk assessments, and 
respond to comments and may request public input on risk mitigation 
before completing proposed registration review decisions for the 
pesticides listed in the Table in Unit III. Through this program, EPA 
is ensuring that each pesticide's registration is based on current 
scientific and other knowledge, including its effects on human health 
and the environment.

DATES: Comments must be received on or before October 2, 2017.

ADDRESSES: Submit your comments, identified by docket identification 
(ID) number EPA-HQ-OPP-2015-0794, by one of the following methods:
     Federal eRulemaking Portal: https://www.regulations.gov. 
Follow the online instructions for submitting comments. Do not submit 
electronically any information you consider to be Confidential Business 
Information (CBI) or other information whose disclosure is restricted 
by statute.
     Mail: OPP Docket, Environmental Protection Agency Docket 
Center (EPA/DC), (28221T), 1200 Pennsylvania Ave. NW., Washington, DC 
20460-0001.
     Hand Delivery: To make special arrangements for hand 
delivery or delivery of boxed information, please follow the 
instructions at https://www.epa.gov/dockets/contacts.html.
    Additional instructions on commenting or visiting the docket, along 
with more information about dockets generally, is available at https://www.epa.gov/dockets.

FOR FURTHER INFORMATION CONTACT: 
    For pesticide specific information contact: The Chemical Review 
Manager identified for the pesticide of interest in the Table in Unit 
III.
    For general questions on the registration review program, contact: 
Dana Friedman, Pesticide Re-Evaluation Division (7508P), Office of 
Pesticide Programs, Environmental Protection Agency, 1200 Pennsylvania 
Ave. NW., Washington, DC 20460-0001; telephone number: (703) 347-8827; 
email address: friedman.dana@epa.gov.

SUPPLEMENTARY INFORMATION: 

I. General Information

A. Does this action apply to me?

    This action is directed to the public in general, and may be of 
interest to a wide range of stakeholders including environmental, human 
health, farm worker, and agricultural advocates; the chemical industry; 
pesticide users; and members of the public interested in the sale, 
distribution, or use of pesticides. Since others also may be 
interested, the Agency has not attempted to describe all the specific 
entities that may be affected by this action. If you have any questions 
regarding the applicability of this action to a particular entity, 
consult the Chemical Review Manager identified for the pesticide of 
interest in the Table in Unit III.

B. What should I consider as I prepare my comments for EPA?

    1. Submitting CBI. Do not submit this information to EPA through 
regulations.gov or email. Clearly mark the part or all of the 
information that you claim to be CBI. For CBI information in a disk or 
CD-ROM that you mail to EPA, mark the outside of the disk or CD-ROM as 
CBI and then identify electronically within the disk or CD-ROM the 
specific information that is claimed as CBI. In addition to one 
complete version of the comment that includes information claimed as 
CBI, a copy of the comment that does not contain the information 
claimed as CBI must be submitted for inclusion in the public docket. 
Information so marked will not be disclosed except in accordance with 
procedures set forth in 40 CFR part 2.
    2. Tips for preparing your comments. When preparing and submitting 
your comments, see the commenting tips at https://www.epa.gov/dockets/comments.html.
    3. Environmental justice. EPA seeks to achieve environmental 
justice, the fair treatment and meaningful involvement of any group, 
including minority and/or low income populations, in the development, 
implementation, and enforcement of environmental laws, regulations, and 
policies. To help address potential environmental justice issues, the 
Agency seeks information on any groups or segments of the population 
who, as a result of their location, cultural practices, or other 
factors, may have atypical or disproportionately high and adverse human 
health impacts or environmental effects from exposure to the pesticides 
discussed in this document, compared to the general population.

II. Authority

    EPA is conducting its registration review of the pesticides listed 
in the Table in Unit III pursuant to section 3(g) of the Federal 
Insecticide, Fungicide, and Rodenticide Act (FIFRA) and the Procedural 
Regulations for Registration Review at 40 CFR part 155, subpart C. 
Section 3(g) of FIFRA provides, among other things, that the 
registrations of pesticides are to be reviewed every 15 years. Under 
FIFRA, a pesticide product may be registered or remain registered only 
if it meets the statutory standard for registration given in FIFRA 
section 3(c)(5) (7 U.S.C. 136a(c)(5)). When used in accordance with 
widespread and commonly recognized practice, the pesticide product must 
perform its intended function without unreasonable adverse effects on 
the environment; that is, without any unreasonable risk to man or the 
environment, or a human dietary risk from residues that result from the 
use of a pesticide in or on food.

III. Registration Reviews

    As directed by FIFRA section 3(g), EPA is reviewing the pesticide 
registrations for the pesticides listed in the Table of this unit to 
ensure that they continue to satisfy the FIFRA standard for 
registration--that is, that these pesticides can still be used without 
unreasonable adverse effects on human health or the environment.

[[Page 36136]]



                      Table--Draft Risk Assessments Being Made Available for Public Comment
----------------------------------------------------------------------------------------------------------------
                                                                                          Chemical Review
  Registration review  case name and             Pesticide Docket ID No.             Manager,telephone number,
                 No.                                                                       email address
----------------------------------------------------------------------------------------------------------------
Benfluralin, Case 2030...............  EPA-HQ-OPP-2011-0931                        Brian Kettl,
                                                                                    kettl.brian@epa.gov, (703)
                                                                                    347-0535.
Bromuconazole, Case 7035.............  EPA-HQ-OPP-2015-0535                        Thomas Harty,
                                                                                    harty.thomas@epa.gov, (703)
                                                                                    347-0338.
Carbaryl, Case 0080..................  EPA-HQ-OPP-2010-0230                        Linsey Walsh,
                                                                                    walsh.linsey@epa.gov, (703)
                                                                                    347-8030.
Clodinafop-propargyl, Case 7250......  EPA-HQ-OPP-2012-0424                        Wilhelmena Livingston,
                                                                                    livingston.wilhelmena@epa.gov, (703) 308-8025.
Deltamethrin, Case 7414..............  EPA-HQ-OPP-2009-0637                        Bilin Basu,
                                                                                    basu.bilin@epa.gov, (703)
                                                                                    347-0455.
Diflufenzopyr, Case 7246.............  EPA-HQ-OPP-2011-0911                        Bilin Basu,
                                                                                    basu.bilin@epa.gov, (703)
                                                                                    347-0455.
Esfenvalerate, Case 7406.............  EPA-HQ-OPP-2009-0301                        Marianne Mannix,
                                                                                    mannix.marianne@epa.gov,
                                                                                    (703) 347-0275.
Lufenuron, Case 7627.................  EPA-HQ-OPP-2015-0098                        Bonnie Adler,
                                                                                    adler.bonnie@epa.gov, (703)
                                                                                    308-8523.
Mepiquat Chloride/Mepiquat             EPA-HQ-OPP-2012-0083                        Caitlin Newcamp,
 Pentaborate, Case 2375.                                                            newcamp.caitlin@epa.gov,
                                                                                    (703) 347-0325.
----------------------------------------------------------------------------------------------------------------

    Pursuant to 40 CFR 155.53(c), EPA is providing an opportunity, 
through this notice of availability, for interested parties to provide 
comments and input concerning the Agency's draft human health and/or 
ecological risk assessments for the pesticides listed in the Table in 
Unit III. Such comments and input could address, among other things, 
the Agency's risk assessment methodologies and assumptions, as applied 
to these draft risk assessments. The Agency will consider all comments 
received during the public comment period and make changes, as 
appropriate, to the draft human health and/or ecological risk 
assessments. EPA will then issue revised risk assessments, explain any 
changes to the draft risk assessments, and respond to comments. In the 
Federal Register notice announcing the availability of the revised risk 
assessments, if the revised risk assessment indicates risks of concern, 
the Agency may provide a comment period for the public to submit 
suggestions for mitigating the risk identified in the revised risk 
assessment before developing proposed registration review decisions for 
the pesticides listed in the Table in Unit III.
    1. Information submission requirements. Anyone may submit data or 
information in response to this document. To be considered during a 
pesticide's registration review, the submitted data or information must 
meet the following requirements:
     To ensure that EPA will consider data or information 
submitted, interested persons must submit the data or information 
during the comment period. The Agency may, at its discretion, consider 
data or information submitted at a later date.
     The data or information submitted must be presented in a 
legible and useable form. For example, an English translation must 
accompany any material that is not in English and a written transcript 
must accompany any information submitted as an audiographic or 
videographic record. Written material may be submitted in paper or 
electronic form.
     Submitters must clearly identify the source of any 
submitted data or information.
     Submitters may request the Agency to reconsider data or 
information that the Agency rejected in a previous review. However, 
submitters must explain why they believe the Agency should reconsider 
the data or information in the pesticide's registration review.
    As provided in 40 CFR 155.58, the registration review docket for 
each pesticide case will remain publicly accessible through the 
duration of the registration review process; that is, until all actions 
required in the final decision on the registration review case have 
been completed.

    Authority:  7 U.S.C. 136 et seq.

    Dated: May 11, 2017.
Yu-Ting Guilaran,
Director, Pesticide Re-Evaluation Division, Office of Pesticide 
Programs.
[FR Doc. 2017-16372 Filed 8-2-17; 8:45 am]
BILLING CODE 6560-50-P
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