Lipochitooligosaccharide (LCO) MOR116; Exemption From the Requirement of a Tolerance, 43703-43705 [2019-17994]
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43703
Federal Register / Vol. 84, No. 163 / Thursday, August 22, 2019 / Rules and Regulations
This action is not a ‘‘major rule’’ as
defined by 5 U.S.C. 804(2).
Under section 307(b)(1) of the CAA,
petitions for judicial review of this
action must be filed in the United States
Court of Appeals for the appropriate
circuit by October 21, 2019. Filing a
petition for reconsideration by the
Administrator of this final rule does not
affect the finality of this action for the
purposes of judicial review nor does it
extend the time within which a petition
for judicial review may be filed, and
shall not postpone the effectiveness of
such rule or action. This action may not
be challenged later in proceedings to
enforce its requirements. (See section
307(b)(2)).
Incorporation by reference,
Intergovernmental relations, Lead,
Nitrogen dioxide, Ozone, Particulate
matter, Reporting and recordkeeping
requirements, Sulfur oxides, Volatile
organic compounds.
PART 52—APPROVAL AND
PROMULGATION OF
IMPLEMENTATION PLANS
1. The authority citation for part 52
continues to read as follows:
■
40 CFR Part 70
Authority: 42 U.S.C. 7401 et seq.
Environmental protection,
Administrative practice and procedure,
Air pollution control, Intergovernmental
relations, Operating permits, Reporting
and recordkeeping requirements.
Dated: August 15, 2019.
Edward Chu,
Acting Regional Administrator, Region 7.
Subpart AA—MISSOURI
2. In § 52.1320, the table in paragraph
(c) is amended by revising the entry for
‘‘10–6.110’’ to read as follows:
■
§ 52.1320
*
Identification of plan.
*
*
(c) * * *
*
*
For the reasons stated in the
preamble, the EPA amends 40 CFR parts
52 and 70 as set forth below:
List of Subjects
40 CFR Part 52
Environmental protection, Air
pollution control, Carbon monoxide,
EPA-APPROVED MISSOURI REGULATIONS
Missouri citation
State
effective
date
Title
EPA approval date
Explanation
Missouri Department of Natural Resources
*
*
*
*
*
*
*
Chapter 6—Air Quality Standards, Definitions, Sampling and Reference Methods, and Air Pollution Control Regulations for the State of
Missouri
*
10–6.110 .................
*
*
Reporting Emission Data, Emission
Fees, and Process Information.
*
*
*
*
*
*
*
1/30/2019
*
*
*
3. The authority citation for part 70
continues to read as follows:
BILLING CODE 6560–50–P
■
4. Appendix A to part 70 is amended
by adding paragraph (hh) under
‘‘Missouri’’ to read as follows:
*
*
*
*
*
*
Lipochitooligosaccharide (LCO)
MOR116; Exemption From the
Requirement of a Tolerance
16:03 Aug 21, 2019
Environmental Protection
Agency (EPA).
ACTION: Final rule.
AGENCY:
(hh) The Missouri Department of Natural
Resources submitted revisions to Missouri
rule 10 CSR 10–6.110, ‘‘Reporting Emission
Data, Emission Fees, and Process
Information’’ on January 15, 2019. The state
effective date is January 30, 2019. Approval
VerDate Sep<11>2014
*
[EPA–HQ–OPP–2018–0244; FRL–9997–94]
Missouri
*
*
40 CFR Part 180
Appendix A to Part 70—Approval
Status of State and Local Operating
Permits Programs
*
*
[FR Doc. 2019–18036 Filed 8–21–19; 8:45 am]
ENVIRONMENTAL PROTECTION
AGENCY
Authority: 42 U.S.C. 7401, et seq.’’
■
*
*
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SUMMARY: This regulation establishes an
exemption from the requirement of a
tolerance for residues of
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*
*
Section (3)(A), Emissions Fees, has not
been approved as part of the SIP.
*
of Section 3(A) of 10 CSR 10–6.110 is
effective September 23, 2019.
*
PART 70—STATE OPERATING PERMIT
PROGRAMS
*
*
8/22/2019, [insert
Federal Register
citation].
Sfmt 4700
*
*
lipochitooliosaccharide (LCO) MOR116
in or on all food commodities when
used in accordance with label directions
and good agricultural practices.
Monsanto Company (now known as
Bayer Crop Science LP), submitted a
petition to EPA under the Federal Food,
Drug, and Cosmetic Act (FFDCA),
requesting an exemption from the
requirement of a tolerance. This
regulation eliminates the need to
establish a maximum permissible level
for residues of LCO MOR116 under
FFDCA.
This regulation is effective
August 22, 2019. Objections and
requests for hearings must be received
on or before October 21, 2019, and must
be filed in accordance with the
instructions provided in 40 CFR part
178 (see also Unit I.C. of the
SUPPLEMENTARY INFORMATION).
DATES:
E:\FR\FM\22AUR1.SGM
22AUR1
43704
Federal Register / Vol. 84, No. 163 / Thursday, August 22, 2019 / Rules and Regulations
The docket for this action,
identified by docket identification (ID)
number EPA–HQ–OPP–2018–0244, 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.
FOR FURTHER INFORMATION CONTACT:
Robert McNally, Biopesticides and
Pollution Prevention Division (7511P),
Office of Pesticide Programs,
Environmental Protection Agency, 1200
Pennsylvania Ave. NW, Washington, DC
20460–0001; main telephone number:
(703) 305–7090; email address:
BPPDFRNotices@epa.gov.
SUPPLEMENTARY INFORMATION:
ADDRESSES:
I. General Information
A. Does this action apply to me?
You may be potentially affected by
this action if you are an agricultural
producer, food manufacturer, or
pesticide manufacturer. The following
list of North American Industrial
Classification System (NAICS) codes is
not intended to be exhaustive, but rather
provides a guide to help readers
determine whether this document
applies to them. Potentially affected
entities may include:
• Crop production (NAICS code 111).
• Animal production (NAICS code
112).
• Food manufacturing (NAICS code
311).
• Pesticide manufacturing (NAICS
code 32532).
B. How can I get electronic access to
other related information?
You may access a frequently updated
electronic version of 40 CFR part 180
through the Government Publishing
Office’s e-CFR site at https://
www.ecfr.gov/cgi-bin/text-idx?&c=
ecfr&tpl=/ecfrbrowse/Title40/40tab_
02.tpl.
C. How can I file an objection or hearing
request?
Under FFDCA section 408(g), 21
U.S.C. 346a(g), any person may file an
objection to any aspect of this regulation
and may also request a hearing on those
VerDate Sep<11>2014
16:03 Aug 21, 2019
Jkt 247001
objections. You must file your objection
or request a hearing on this regulation
in accordance with the instructions
provided in 40 CFR part 178. To ensure
proper receipt by EPA, you must
identify docket ID number EPA–HQ–
OPP–2017–0487 in the subject line on
the first page of your submission. All
objections and requests for a hearing
must be in writing and must be received
by the Hearing Clerk on or before
October 21, 2019. Addresses for mail
and hand delivery of objections and
hearing requests are provided in 40 CFR
178.25(b).
In addition to filing an objection or
hearing request with the Hearing Clerk
as described in 40 CFR part 178, please
submit a copy of the filing (excluding
any Confidential Business Information
(CBI)) for inclusion in the public docket.
Information not marked confidential
pursuant to 40 CFR part 2 may be
disclosed publicly by EPA without prior
notice. Submit the non-CBI copy of your
objection or hearing request, identified
by docket ID number EPA–HQ–OPP–
2018–0244, 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 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.
II. Background
In the Federal Register of July 24,
2018 (83 FR 34968) (FRL–9980–31),
EPA issued a document pursuant to
FFDCA section 408(d)(3), 21 U.S.C.
346a(d)(3), announcing the filing of a
pesticide tolerance petition (PP 8F8670)
by Monsanto Company (now known as
Bayer Crop Science LP), 800 N.
Lindbergh Blvd., St. Louis, MO 63167.
The petition requested that 40 CFR part
180 be amended by establishing an
exemption from the requirement of a
tolerance for residues of LCO MOR116
in or on all food commodities. That
document referenced a summary of the
petition prepared by the petitioner,
Monsanto Company (now known as
PO 00000
Frm 00038
Fmt 4700
Sfmt 4700
Bayer Crop Science LP), which is
available in the docket via https://
www.regulations.gov. There were no
comments received in response to the
notice of filing.
III. Final Rule
A. EPA’s Safety Determination
Section 408(c)(2)(A)(i) of FFDCA
allows EPA to establish an exemption
from the requirement for a tolerance (the
legal limit for a pesticide chemical
residue in or on a food) only if EPA
determines that the exemption is ‘‘safe.’’
Section 408(c)(2)(A)(ii) of FFDCA
defines ‘‘safe’’ to mean that ‘‘there is a
reasonable certainty that no harm will
result from aggregate exposure to the
pesticide chemical residue, including
all anticipated dietary exposures and all
other exposures for which there is
reliable information.’’ This includes
exposure through drinking water and in
residential settings but does not include
occupational exposure. Pursuant to
FFDCA section 408(c)(2)(B), in
establishing or maintaining in effect an
exemption from the requirement of a
tolerance, EPA must take into account
the factors set forth in FFDCA section
408(b)(2)(C), which require EPA to give
special consideration to exposure of
infants and children to the pesticide
chemical residue in establishing a
tolerance or tolerance exemption, and to
‘‘ensure that there is a reasonable
certainty that no harm will result to
infants and children from aggregate
exposure to the pesticide chemical
residue . . . .’’ Additionally, FFDCA
section 408(b)(2)(D) requires that EPA
consider ‘‘available information
concerning the cumulative effects of [a
particular pesticide’s] . . . residues and
other substances that have a common
mechanism of toxicity.’’
EPA evaluated the available toxicity
and exposure data on LCO MOR116 and
considered its validity, completeness,
and reliability, as well as the
relationship of this information to
human risk. EPA also considered
available information concerning the
variability of the sensitivities of major
identifiable subgroups of consumers,
including infants and children.
LCO MOR116 a synthetically derived
member of the lipochitooligosaccharide
(LCO) chemical class. Naturally
occurring LCOs function as signaling
molecules in the initiation of plantmicrobe endosymbioses in an estimated
70–80% of land plants. As a
biopesticide, LCO MOR116 is intended
to be used as a plant growth regulator
(PGR) to increase growth and decrease
stress in growing crops. LCO MOR116
has low acute toxicity, low subchronic
E:\FR\FM\22AUR1.SGM
22AUR1
Federal Register / Vol. 84, No. 163 / Thursday, August 22, 2019 / Rules and Regulations
toxicity and is not a skin sensitizer or
mutagen based on the toxicity
information presented for the active
ingredient and structurally-similar
compounds. Dietary and drinking water
exposure to LCO MOR116 is not
expected for the proposed use as a seed
treatment for soybean and application
rates are expected to be very low (5.89
X 10–11 lb ai/lb seed). Although no
field trial or residue data are available,
significant residues are not expected
and, therefore, quantitative dietary and
drinking water assessments were not
conducted.
There are currently no residential
uses proposed for LCO MOR116. There
is a potential for occupational exposure,
however, no toxicological endpoints
have been identified. The Agency has
determined that no further acute or
subchronic toxicity studies are needed
at this time considering all the available
hazard and exposure data on LCOs and
structurally similar compounds. Based
on the available toxicity and exposure
information, no unreasonable adverse
effects to the U.S. population in general,
and to infants and children in
particular, will result from the use of
LCO MOR116 as a pesticide when label
instructions are followed.
An explanation of the data upon
which EPA relied and its risk
assessment based on those data can be
found within the (July 30, 2019),
document entitled ‘‘Federal Food, Drug,
and Cosmetic Act (FFDCA) Safety
Assessment for Exemption from the
Requirement of a Tolerance for Residues
of Lipochitooligosaccharide (LCO)
MOR116.’’ This document, as well as
other relevant information, is available
in the docket for this action as described
under ADDRESSES.
Based on its safety determination,
EPA is establishing an exemption from
the requirement of a tolerance for
residues of LCO MOR116 in or on all
food commodities when used on
accordance with label directions and
good agricultural practices.
B. Analytical Enforcement Methodology
An analytical method is not required
for enforcement purposes due to lack of
concern for exposures, which supports
the establishment of an exemption for
residues of LCO MOR116.
IV. Statutory and Executive Order
Reviews
This action establishes a tolerance
exemption under FFDCA section 408(d)
in response to a petition submitted to
EPA. The Office of Management and
Budget (OMB) has exempted these types
of actions from review under Executive
Order 12866, entitled ‘‘Regulatory
VerDate Sep<11>2014
16:03 Aug 21, 2019
Jkt 247001
Planning and Review’’ (58 FR 51735,
October 4, 1993). Because this action
has been exempted from review under
Executive Order 12866, this action is
not subject to Executive Order 13211,
entitled ‘‘Actions Concerning
Regulations That Significantly Affect
Energy Supply, Distribution, or Use’’ (66
FR 28355, May 22, 2001), or Executive
Order 13045, entitled ‘‘Protection of
Children from Environmental Health
Risks and Safety Risks’’ (62 FR 19885,
April 23, 1997), nor is it a regulatory
action under Executive Order 13771,
entitled ‘‘Reducing Regulations and
Controlling Regulatory Costs’’ (82 FR
9339, February 3, 2017). This action
does not contain any information
collections subject to OMB approval
under the Paperwork Reduction Act
(PRA), 44 U.S.C. 3501 et seq., nor does
it require any special considerations
under Executive Order 12898, entitled
‘‘Federal Actions to Address
Environmental Justice in Minority
Populations and Low-Income
Populations’’ (59 FR 7629, February 16,
1994).
Since tolerances and exemptions that
are established on the basis of a petition
under FFDCA section 408(d), such as
the tolerance exemption in this action,
do not require the issuance of a
proposed rule, the requirements of the
Regulatory Flexibility Act (RFA) (5
U.S.C. 601 et seq.) do not apply.
This action directly regulates growers,
food processors, food handlers, and food
retailers, not States or tribes. As a result,
this action does not alter the
relationships or distribution of power
and responsibilities established by
Congress in the preemption provisions
of FFDCA section 408(n)(4). As such,
EPA has determined that this action will
not have a substantial direct effect on
States or tribal governments, on the
relationship between the national
government and the States or tribal
governments, or on the distribution of
power and responsibilities among the
various levels of government or between
the Federal Government and Indian
tribes. Thus, EPA has determined that
Executive Order 13132, entitled
‘‘Federalism’’ (64 FR 43255, August 10,
1999), and Executive Order 13175,
entitled ‘‘Consultation and Coordination
with Indian Tribal Governments’’ (65 FR
67249, November 9, 2000), do not apply
to this action. In addition, this action
does not impose any enforceable duty or
contain any unfunded mandate as
described under Title II of the Unfunded
Mandates Reform Act (UMRA) (2 U.S.C.
1501 et seq.).
This action does not involve any
technical standards that would require
EPA’s consideration of voluntary
PO 00000
Frm 00039
Fmt 4700
Sfmt 4700
43705
consensus standards pursuant to section
12(d) of the National Technology
Transfer and Advancement Act
(NTTAA) (15 U.S.C. 272 note).
V. Congressional Review Act
Pursuant to the Congressional Review
Act (5 U.S.C. 801 et seq.), EPA will
submit a report containing this rule and
other required information to the U.S.
Senate, the U.S. House of
Representatives, and the Comptroller
General of the United States prior to
publication of the rule in the Federal
Register. This action is not a ‘‘major
rule’’ as defined by 5 U.S.C. 804(2).
List of Subjects in 40 CFR Part 180
Environmental protection,
Administrative practice and procedure,
Agricultural commodities, Pesticides
and pests, Reporting and recordkeeping
requirements.
Dated: August 7, 2019
Richard Keigwin,
Director, Office of Pesticide Programs.
Therefore, 40 CFR chapter I is
amended as follows:
PART 180—[AMENDED]
1. The authority citation for part 180
continues to read as follows:
■
Authority: 21 U.S.C. 321(q), 346a and 371.
2. Add § 180.1370 to subpart D to read
as follows:
■
§ 180.1370 Lipochitoolgiosaccharide
(LCO) MOR116; exemption from the
requirement of a tolerance.
Residues of the plant growth regulator
Lipochitoolgiosaccharide (LCO)
MOR116 in or on all food commodities
are exempt from the requirement of a
tolerance, when used in accordance
with label directions and good
agricultural practices.
[FR Doc. 2019–17994 Filed 8–21–19; 8:45 am]
BILLING CODE 6560–50–P
FEDERAL COMMUNICATIONS
COMMISSION
47 CFR Parts 1, 43, and 54
[WC Docket Nos. 11–10 and 19–195, FCC
No. 19–79]
Establishing the Digital Opportunity
Data Collection and Modernizing the
FCC Form 477 Data Program
Federal Communications
Commission.
ACTION: Final rule.
AGENCY:
SUMMARY: In this document, the Federal
Communications Commission
E:\FR\FM\22AUR1.SGM
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Agencies
[Federal Register Volume 84, Number 163 (Thursday, August 22, 2019)]
[Rules and Regulations]
[Pages 43703-43705]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2019-17994]
-----------------------------------------------------------------------
ENVIRONMENTAL PROTECTION AGENCY
40 CFR Part 180
[EPA-HQ-OPP-2018-0244; FRL-9997-94]
Lipochitooligosaccharide (LCO) MOR116; Exemption From the
Requirement of a Tolerance
AGENCY: Environmental Protection Agency (EPA).
ACTION: Final rule.
-----------------------------------------------------------------------
SUMMARY: This regulation establishes an exemption from the requirement
of a tolerance for residues of lipochitooliosaccharide (LCO) MOR116 in
or on all food commodities when used in accordance with label
directions and good agricultural practices. Monsanto Company (now known
as Bayer Crop Science LP), submitted a petition to EPA under the
Federal Food, Drug, and Cosmetic Act (FFDCA), requesting an exemption
from the requirement of a tolerance. This regulation eliminates the
need to establish a maximum permissible level for residues of LCO
MOR116 under FFDCA.
DATES: This regulation is effective August 22, 2019. Objections and
requests for hearings must be received on or before October 21, 2019,
and must be filed in accordance with the instructions provided in 40
CFR part 178 (see also Unit I.C. of the SUPPLEMENTARY INFORMATION).
[[Page 43704]]
ADDRESSES: The docket for this action, identified by docket
identification (ID) number EPA-HQ-OPP-2018-0244, 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.
FOR FURTHER INFORMATION CONTACT: Robert McNally, Biopesticides and
Pollution Prevention Division (7511P), Office of Pesticide Programs,
Environmental Protection Agency, 1200 Pennsylvania Ave. NW, Washington,
DC 20460-0001; main telephone number: (703) 305-7090; email address:
[email protected].
SUPPLEMENTARY INFORMATION:
I. General Information
A. Does this action apply to me?
You may be potentially affected by this action if you are an
agricultural producer, food manufacturer, or pesticide manufacturer.
The following list of North American Industrial Classification System
(NAICS) codes is not intended to be exhaustive, but rather provides a
guide to help readers determine whether this document applies to them.
Potentially affected entities may include:
Crop production (NAICS code 111).
Animal production (NAICS code 112).
Food manufacturing (NAICS code 311).
Pesticide manufacturing (NAICS code 32532).
B. How can I get electronic access to other related information?
You may access a frequently updated electronic version of 40 CFR
part 180 through the Government Publishing Office's e-CFR site at
https://www.ecfr.gov/cgi-bin/text-idx?&c=ecfr&tpl=/ecfrbrowse/Title40/40tab_02.tpl.
C. How can I file an objection or hearing request?
Under FFDCA section 408(g), 21 U.S.C. 346a(g), any person may file
an objection to any aspect of this regulation and may also request a
hearing on those objections. You must file your objection or request a
hearing on this regulation in accordance with the instructions provided
in 40 CFR part 178. To ensure proper receipt by EPA, you must identify
docket ID number EPA-HQ-OPP-2017-0487 in the subject line on the first
page of your submission. All objections and requests for a hearing must
be in writing and must be received by the Hearing Clerk on or before
October 21, 2019. Addresses for mail and hand delivery of objections
and hearing requests are provided in 40 CFR 178.25(b).
In addition to filing an objection or hearing request with the
Hearing Clerk as described in 40 CFR part 178, please submit a copy of
the filing (excluding any Confidential Business Information (CBI)) for
inclusion in the public docket. Information not marked confidential
pursuant to 40 CFR part 2 may be disclosed publicly by EPA without
prior notice. Submit the non-CBI copy of your objection or hearing
request, identified by docket ID number EPA-HQ-OPP-2018-0244, 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 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.
II. Background
In the Federal Register of July 24, 2018 (83 FR 34968) (FRL-9980-
31), EPA issued a document pursuant to FFDCA section 408(d)(3), 21
U.S.C. 346a(d)(3), announcing the filing of a pesticide tolerance
petition (PP 8F8670) by Monsanto Company (now known as Bayer Crop
Science LP), 800 N. Lindbergh Blvd., St. Louis, MO 63167. The petition
requested that 40 CFR part 180 be amended by establishing an exemption
from the requirement of a tolerance for residues of LCO MOR116 in or on
all food commodities. That document referenced a summary of the
petition prepared by the petitioner, Monsanto Company (now known as
Bayer Crop Science LP), which is available in the docket via https://www.regulations.gov. There were no comments received in response to the
notice of filing.
III. Final Rule
A. EPA's Safety Determination
Section 408(c)(2)(A)(i) of FFDCA allows EPA to establish an
exemption from the requirement for a tolerance (the legal limit for a
pesticide chemical residue in or on a food) only if EPA determines that
the exemption is ``safe.'' Section 408(c)(2)(A)(ii) of FFDCA defines
``safe'' to mean that ``there is a reasonable certainty that no harm
will result from aggregate exposure to the pesticide chemical residue,
including all anticipated dietary exposures and all other exposures for
which there is reliable information.'' This includes exposure through
drinking water and in residential settings but does not include
occupational exposure. Pursuant to FFDCA section 408(c)(2)(B), in
establishing or maintaining in effect an exemption from the requirement
of a tolerance, EPA must take into account the factors set forth in
FFDCA section 408(b)(2)(C), which require EPA to give special
consideration to exposure of infants and children to the pesticide
chemical residue in establishing a tolerance or tolerance exemption,
and to ``ensure that there is a reasonable certainty that no harm will
result to infants and children from aggregate exposure to the pesticide
chemical residue . . . .'' Additionally, FFDCA section 408(b)(2)(D)
requires that EPA consider ``available information concerning the
cumulative effects of [a particular pesticide's] . . . residues and
other substances that have a common mechanism of toxicity.''
EPA evaluated the available toxicity and exposure data on LCO
MOR116 and considered its validity, completeness, and reliability, as
well as the relationship of this information to human risk. EPA also
considered available information concerning the variability of the
sensitivities of major identifiable subgroups of consumers, including
infants and children.
LCO MOR116 a synthetically derived member of the
lipochitooligosaccharide (LCO) chemical class. Naturally occurring LCOs
function as signaling molecules in the initiation of plant-microbe
endosymbioses in an estimated 70-80% of land plants. As a biopesticide,
LCO MOR116 is intended to be used as a plant growth regulator (PGR) to
increase growth and decrease stress in growing crops. LCO MOR116 has
low acute toxicity, low subchronic
[[Page 43705]]
toxicity and is not a skin sensitizer or mutagen based on the toxicity
information presented for the active ingredient and structurally-
similar compounds. Dietary and drinking water exposure to LCO MOR116 is
not expected for the proposed use as a seed treatment for soybean and
application rates are expected to be very low (5.89 X 10-11 lb ai/lb
seed). Although no field trial or residue data are available,
significant residues are not expected and, therefore, quantitative
dietary and drinking water assessments were not conducted.
There are currently no residential uses proposed for LCO MOR116.
There is a potential for occupational exposure, however, no
toxicological endpoints have been identified. The Agency has determined
that no further acute or subchronic toxicity studies are needed at this
time considering all the available hazard and exposure data on LCOs and
structurally similar compounds. Based on the available toxicity and
exposure information, no unreasonable adverse effects to the U.S.
population in general, and to infants and children in particular, will
result from the use of LCO MOR116 as a pesticide when label
instructions are followed.
An explanation of the data upon which EPA relied and its risk
assessment based on those data can be found within the (July 30, 2019),
document entitled ``Federal Food, Drug, and Cosmetic Act (FFDCA) Safety
Assessment for Exemption from the Requirement of a Tolerance for
Residues of Lipochitooligosaccharide (LCO) MOR116.'' This document, as
well as other relevant information, is available in the docket for this
action as described under ADDRESSES.
Based on its safety determination, EPA is establishing an exemption
from the requirement of a tolerance for residues of LCO MOR116 in or on
all food commodities when used on accordance with label directions and
good agricultural practices.
B. Analytical Enforcement Methodology
An analytical method is not required for enforcement purposes due
to lack of concern for exposures, which supports the establishment of
an exemption for residues of LCO MOR116.
IV. Statutory and Executive Order Reviews
This action establishes a tolerance exemption under FFDCA section
408(d) in response to a petition submitted to EPA. The Office of
Management and Budget (OMB) has exempted these types of actions from
review under Executive Order 12866, entitled ``Regulatory Planning and
Review'' (58 FR 51735, October 4, 1993). Because this action has been
exempted from review under Executive Order 12866, this action is not
subject to Executive Order 13211, entitled ``Actions Concerning
Regulations That Significantly Affect Energy Supply, Distribution, or
Use'' (66 FR 28355, May 22, 2001), or Executive Order 13045, entitled
``Protection of Children from Environmental Health Risks and Safety
Risks'' (62 FR 19885, April 23, 1997), nor is it a regulatory action
under Executive Order 13771, entitled ``Reducing Regulations and
Controlling Regulatory Costs'' (82 FR 9339, February 3, 2017). This
action does not contain any information collections subject to OMB
approval under the Paperwork Reduction Act (PRA), 44 U.S.C. 3501 et
seq., nor does it require any special considerations under Executive
Order 12898, entitled ``Federal Actions to Address Environmental
Justice in Minority Populations and Low-Income Populations'' (59 FR
7629, February 16, 1994).
Since tolerances and exemptions that are established on the basis
of a petition under FFDCA section 408(d), such as the tolerance
exemption in this action, do not require the issuance of a proposed
rule, the requirements of the Regulatory Flexibility Act (RFA) (5
U.S.C. 601 et seq.) do not apply.
This action directly regulates growers, food processors, food
handlers, and food retailers, not States or tribes. As a result, this
action does not alter the relationships or distribution of power and
responsibilities established by Congress in the preemption provisions
of FFDCA section 408(n)(4). As such, EPA has determined that this
action will not have a substantial direct effect on States or tribal
governments, on the relationship between the national government and
the States or tribal governments, or on the distribution of power and
responsibilities among the various levels of government or between the
Federal Government and Indian tribes. Thus, EPA has determined that
Executive Order 13132, entitled ``Federalism'' (64 FR 43255, August 10,
1999), and Executive Order 13175, entitled ``Consultation and
Coordination with Indian Tribal Governments'' (65 FR 67249, November 9,
2000), do not apply to this action. In addition, this action does not
impose any enforceable duty or contain any unfunded mandate as
described under Title II of the Unfunded Mandates Reform Act (UMRA) (2
U.S.C. 1501 et seq.).
This action does not involve any technical standards that would
require EPA's consideration of voluntary consensus standards pursuant
to section 12(d) of the National Technology Transfer and Advancement
Act (NTTAA) (15 U.S.C. 272 note).
V. Congressional Review Act
Pursuant to the Congressional Review Act (5 U.S.C. 801 et seq.),
EPA will submit a report containing this rule and other required
information to the U.S. Senate, the U.S. House of Representatives, and
the Comptroller General of the United States prior to publication of
the rule in the Federal Register. This action is not a ``major rule''
as defined by 5 U.S.C. 804(2).
List of Subjects in 40 CFR Part 180
Environmental protection, Administrative practice and procedure,
Agricultural commodities, Pesticides and pests, Reporting and
recordkeeping requirements.
Dated: August 7, 2019
Richard Keigwin,
Director, Office of Pesticide Programs.
Therefore, 40 CFR chapter I is amended as follows:
PART 180--[AMENDED]
0
1. The authority citation for part 180 continues to read as follows:
Authority: 21 U.S.C. 321(q), 346a and 371.
0
2. Add Sec. 180.1370 to subpart D to read as follows:
Sec. 180.1370 Lipochitoolgiosaccharide (LCO) MOR116; exemption from
the requirement of a tolerance.
Residues of the plant growth regulator Lipochitoolgiosaccharide
(LCO) MOR116 in or on all food commodities are exempt from the
requirement of a tolerance, when used in accordance with label
directions and good agricultural practices.
[FR Doc. 2019-17994 Filed 8-21-19; 8:45 am]
BILLING CODE 6560-50-P