Pyriofenone; Pesticide Tolerances, 17545-17548 [2021-06271]
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Federal Register / Vol. 86, No. 63 / Monday, April 5, 2021 / Rules and Regulations
List of Subjects in 40 CFR Part 62
Environmental protection,
Administrative practice and procedure,
Air pollution control, Intergovernmental
relations, Reporting and recordkeeping
requirements, Waste treatment and
disposal.
Dated: March 24, 2021.
David Gray,
Acting Regional Administrator, Region 6.
For the reasons stated in the
preamble, the Environmental Protection
Agency amends 40 CFR part 62 as
follows:
PART 62—APPROVAL AND
PROMULGATION OF STATE PLANS
FOR DESIGNATED FACILITIES AND
POLLUTANTS
1. The authority citation for part 62
continues to read as follows:
■
Authority: 42 U.S.C. 7401 et seq.
Subpart GG—New Mexico
2. Add an undesignated center
heading and § 62.7893 to read as
follows:
■
Emissions From Existing Other Solid
Waste Incineration Units
§ 62.7893 Identification of plan—negative
declarations.
Letters from the New Mexico
Environment Department and the City
of Albuquerque Environmental Health
Department dated June 15, 2020, and
December 13, 2006, respectively,
certifying that there are no incinerators
subject to the Other Solid Waste
Incineration units (OSWI) Emission
Guidelines, at 40 CFR part 60, subpart
FFFF, within their respective
jurisdictions in the State of New
Mexico.
[FR Doc. 2021–06526 Filed 4–2–21; 8:45 am]
under the Federal Food, Drug, and
Cosmetic Act (FFDCA).
DATES: This regulation is effective April
5, 2021. Objections and requests for
hearings must be received on or before
May 5, 2021, and must be filed in
accordance with the instructions
provided in 40 CFR part 178 (see also
Unit I.C. of the SUPPLEMENTARY
INFORMATION).
The docket for this action,
identified by docket identification (ID)
number EPA–HQ–OPP–2020–0335, 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.
Due to the public health concerns
related to COVID–19, the EPA Docket
Center (EPA/DC) and Reading Room is
closed to visitors with limited
exceptions. The staff continues to
provide remote customer service via
email, phone, and webform. For the
latest status information on EPA/DC
services and docket access, visit https://
www.epa.gov/dockets.
FOR FURTHER INFORMATION CONTACT:
Marietta Echeverria, Registration
Division (7505P), Office of Pesticide
Programs, Environmental Protection
Agency, 1200 Pennsylvania Ave. NW,
Washington, DC 20460–0001; main
telephone number: (703) 305–7090;
email address: RDFRNotices@epa.gov.
SUPPLEMENTARY INFORMATION:
ADDRESSES:
I. General Information
BILLING CODE 6560–50–P
A. Does this action apply to me?
ENVIRONMENTAL PROTECTION
AGENCY
40 CFR Part 180
[EPA–HQ–OPP–2020–0335; FRL–10019–55]
Pyriofenone; Pesticide Tolerances
Environmental Protection
Agency (EPA).
ACTION: Final rule.
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AGENCY:
This regulation establishes
tolerances for residues of pyriofenone in
or on fruit, small vine climbing
subgroup 13–07E, except grape; grape
and grape, raisin. ISK BIOSCIENCES
Corporation requested these tolerances
SUMMARY:
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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).
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B. How can I get electronic access to
other related information?
You may access a frequently updated
electronic version of EPA’s tolerance
regulations at 40 CFR part 180 through
the Government Publishing Office’s eCFR site at https://www.ecfr.gov/cgi-bin/
text-idx?&c=ecfr&tpl=/ecfrbrowse/
Title40/40tab_02.tpl. To access the
OCSPP test guidelines referenced in this
document electronically, please go to
https://www.epa.gov/ocspp and select
‘‘Test Methods and Guidelines.’’
C. How can I file an objection or hearing
request?
Under FFDCA section 408(g), 21
U.S.C. 346a, 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–2020–0335 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 June
4, 2021. 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–
2020–0335, 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
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dockets generally, is available at https://
www.epa.gov/dockets.
II. Summary of Petitioned-For
Tolerance
In the Federal Register of August 5,
2020 (85 FR 47330) (FRL–10012–32),
EPA issued a document pursuant to
FFDCA section 408(d)(3), 21 U.S.C.
346a(d)(3), announcing the filing of a
pesticide petition (PP 9F8808) by ISK
BIOSCIENCES Corporation, 7470
Auburn Road, Suite A, Concord, OH,
44077. The petition requested that 40
CFR 180.660 be amended by
establishing tolerances for residues of
the fungicide, pyriofenone, (5-chloro-2methoxy-4-methyl-3-pyridinyl)(2,3,4trimethoxy-6-methylphenyl)
methanone, in or on fruit, small vine
climbing subgroup 13–07E, except grape
at 1.5 parts per million (ppm); grape at
0.8 ppm; and grape, raisin at 2.5 ppm.
In addition, although not mentioned in
EPA’s document, ISK’s petition also
requested that the currently established
tolerances for residues of pyriofenone
in/on fruit, small vine climbing
subgroup 13–07D at 1.5 ppm be
removed from 40 CFR 180.660, as
establishment of the requested
tolerances for subgroup 13–07E and
grape include all the crops in subgroup
13–07D. That document referenced a
summary of the petition prepared by
ISK BIOSCIENCES Corporation, the
registrant, which is available in the
docket, https://www.regulations.gov. No
comment was received in response to
the notice of filing.
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III. Aggregate Risk Assessment and
Determination of Safety
Section 408(b)(2)(A)(i) of FFDCA
allows EPA to establish a tolerance (the
legal limit for a pesticide chemical
residue in or on a food) only if EPA
determines that the tolerance is ‘‘safe.’’
Section 408(b)(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. Section
408(b)(2)(C) of FFDCA requires EPA to
give special consideration to exposure
of infants and children to the pesticide
chemical residue in establishing a
tolerance 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. . . .’’
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Consistent with FFDCA section
408(b)(2)(D), and the factors specified in
FFDCA section 408(b)(2)(D), EPA has
reviewed the available scientific data
and other relevant information in
support of this action. EPA has
sufficient data to assess the hazards of
and to make a determination on
aggregate exposure for pyriofenone
including exposure resulting from the
tolerances established by this action.
EPA’s assessment of exposures and risks
associated with pyriofenone follows.
In an effort to streamline its
publications in the Federal Register,
EPA is not reprinting sections that
repeat what has been previously
published for tolerance rulemakings of
the same pesticide chemical. Where
scientific information concerning a
particular chemical remains unchanged,
the content of those sections would not
vary between tolerance rulemakings,
and republishing the same sections is
unnecessary; therefore, EPA considers
referral back to those sections as
sufficient to provide an explanation of
the information EPA considered in
making its safety determination for the
new rulemaking.
EPA has previously published a
number of tolerance rulemakings for
pyriofenone, in which EPA concluded,
based on the available information, that
there is a reasonable certainty that no
harm would result from aggregate
exposure to pyriofenone and established
tolerances for residues of that chemical.
EPA is incorporating previously
published sections from those
rulemakings as described further in this
rulemaking, as they remain unchanged.
Toxicological Profile. For a discussion
of the Toxicological Profile of
pyriofenone, see Unit III.A. of the May
30, 2019 rulemaking (84 FR 24983)
(FRL–9993–11).
Toxicological Points of Departure/
Levels of Concern. For a summary of the
Toxicological Points of Departure/
Levels of Concern used for the safety
assessment, see Unit III.B. of the May
30, 2019 rulemaking.
Exposure Assessment. EPA’s exposure
assessment remains unchanged from
what was done in support of the May
30, 2019 rulemaking. EPA’s aggregate
exposure assessments include exposures
from food, drinking water and
residential sources, and there have been
no changes since the last assessment.
For a discussion of EPA’s assessment of
aggregate exposures, see Unit III.C. of
the May 30, 2019 rulemaking.
Safety Factor for Infants and
Children. EPA continues to conclude
that there is reliable data showing that
the safety of infants and children would
be adequately protected if the FQPA SF
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were reduced from 10X to 1X for all
exposure scenarios. The reasons for that
decision are articulated in Unit III.D. of
the May 30, 2019 rulemaking.
Aggregate Risks and Determination of
Safety. EPA determines whether acute
and chronic dietary pesticide exposures
are safe by comparing aggregate
exposure estimates to the acute PAD
(aPAD) and chronic PAD (cPAD).
Short-, intermediate-, and chronic-term
risks are evaluated by comparing the
estimated aggregate food, water, and
residential exposure to the appropriate
PODs to ensure that an adequate MOE
exists. For linear cancer risks, EPA
calculates the lifetime probability of
acquiring cancer given the estimated
aggregate exposure.
Pyriofenone is not expected to pose
an acute risk, due to the lack of acute
adverse effects in the database. Chronic
dietary risks are below the Agency’s
level of concern: 6.9% of the chronic
population adjusted dose (cPAD) for
children 1 to 2 years old, the group with
the highest exposure. There are no
residential uses for pyriofenone;
therefore, the chronic aggregate risk is
limited to the chronic dietary risk and
is not of concern. Short- and
intermediate-term aggregate risks are
addressed by the chronic aggregate risk
estimates and are not a concern.
Therefore, based on the risk
assessments and information described
above, EPA concludes there is a
reasonable certainty that no harm will
result to the general populations, or to
infants and children for aggregate
exposure to pyriofenone residues. More
detailed information on the subject
action can be found at https://
www.regulations.gov in the document
entitled, ‘‘Pyriofenone. Human Health
Risk Assessment for the Section 3
Registration on Fruiting Vegetables
(Crop Group 8–10)’’ in the docket ID
number EPA–HQ–OPP–2020–0335 and
the document titled, ‘‘Pyriofenone.
Human Health Risk Assessment for the
Section 3 Registration on Fruiting
Vegetables (Crop Group 8–10)’’ in
docket ID number EPA–HQ–OPP–2018–
0677.
IV. Other Considerations
A. Analytical Enforcement Methodology
For a discussion of the available
analytical enforcement method, see Unit
IV.A. of the May 30, 2019 rulemaking.
B. International Residue Limits
In making its tolerance decisions, EPA
seeks to harmonize U.S. tolerances with
international standards whenever
possible, consistent with U.S. food
safety standards and agricultural
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practices. EPA considers the
international maximum residue limits
(MRLs) established by the Codex
Alimentarius Commission (Codex), as
required by FFDCA section 408(b)(4).
The Codex Alimentarius is a joint
United Nations Food and Agriculture
Organization/World Health
Organization food standards program,
and it is recognized as an international
food safety standards-setting
organization in trade agreements to
which the United States is a party. EPA
may establish a tolerance that is
different from a Codex MRL; however,
FFDCA section 408(b)(4) requires that
EPA explain the reasons for departing
from the Codex level.
The Codex has established MRLs for
pyriofenone in or on grape at 0.8 ppm
and grape, raisin at 2.5 ppm. The U.S.
tolerances for these commodities are
harmonized with these MRLs.
and residues on other commodities in
that subgroup will need to comply with
the new subgroup 13–07E tolerance.
This reduction in tolerance level is
not discriminatory; the same food safety
standard contained in the FFDCA
applies equally to domestically
produced and imported foods. The new
tolerance level is supported by available
residue data.
C. Revisions to Petitioned-For
Tolerances
Under FFDCA section 408(d)(4)(A)(i),
EPA may establish tolerances that vary
from those sought by the petition. The
tolerance level has been modified to be
consistent with the Agency’s rounding
class practices.
VI. Statutory and Executive Order
Reviews
This action establishes and modifies
tolerances under FFDCA section 408(d)
in response to a petition submitted to
the Agency. 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 considered 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 in this final rule, 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.
D. International Trade Considerations
In this Final Rule, EPA is establishing
an individual tolerance for grape at 0.8
ppm, which is lower than the current
allowed amount of residue on grape, by
virtue of its inclusion in the small vine
climbing fruit subgroup 13–07D at 1.5
ppm. The Agency is reducing this
tolerance to harmonize with the Codex
MRL on grape, and available residue
data demonstrate that this tolerance is
sufficient to cover residues on this
commodity.
In accordance with the World Trade
Organization’s (WTO) Sanitary and
Phytosanitary Measures (SPS)
Agreement, EPA intends to notify the
WTO of this revision. In addition, the
SPS Agreement requires that Members
provide a ‘‘reasonable interval’’ between
the publication of a regulation subject to
the Agreement and its entry into force
to allow time for producers in exporting
Member countries to adapt to the new
requirement. To accommodate this
reasonable interval, EPA is establishing
an expiration date for the existing
tolerance for small vine climbing fruit
subgroup 13–07D to allow those
tolerances to remain in effect for a
period of 6 months after the effective
date of this rule. At the end of that 6month period, the existing tolerances for
subgroup 13–07D will no longer be
valid; residues on grape will need to
comply with the new grape tolerance
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V. Conclusion
Therefore, tolerances are established
for residues of pyriofenone, (5-chloro-2methoxy-4-methyl-3-pyridinyl)(2,3,4trimethoxy-6-methylphenyl)
methanone, in or on fruit, small vine
climbing subgroup 13–07E, except grape
at 1.5 ppm; grape at 0.8 ppm; and grape,
raisin at 2.5 ppm. EPA is also
establishing an expiration date for the
existing tolerance for fruit, small vine
climbing subgroup 13–07D.
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17547
This action directly regulates growers,
food processors, food handlers, and food
retailers, not States or Tribes, nor does
this action alter the relationships or
distribution of power and
responsibilities established by Congress
in the preemption provisions of FFDCA
section 408(n)(4). As such, the Agency
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, the Agency 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
Agency 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).
VII. 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: March 8, 2021.
Marietta Echeverria,
Acting Director, Registration Division, Office
of Pesticide Programs.
Therefore, for the reasons stated in the
preamble, EPA is amending 40 CFR
chapter I as follows:
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PART 180—TOLERANCES AND
EXEMPTIONS FOR PESTICIDE
CHEMICAL RESIDUES IN FOOD
1. The authority citation for part 180
continues to read as follows:
■
Authority: 21 U.S.C. 321(q), 346a and 371.
2. In § 180.660, amend the table in
paragraph (a) by:
■ a. Designating the table as Table 1;
■ b. Revising the entry for ‘‘Fruit, small
vine climbing, subgroup 13–07D’’; and
■ c. Adding in alphabetical order entries
for ‘‘Fruit, small vine climbing,
subgroup 13–07E, except grape’’;
‘‘Grape’’; and ‘‘Grape, raisin’’.
The additions and revision read as
follows:
■
§ 180.660 Pyriofenone; tolerances for
residues.
*
*
*
*
*
TABLE 1 TO PARAGRAPH (a)
Parts
per
million
Commodity
*
*
*
*
Fruit, small vine climbing subgroup 13–
1
07D ......................................................
Fruit, small vine climbing subgroup 13–
07E, except grape .................................
Grape .........................................................
Grape, raisin ..............................................
*
1 This
*
*
*
*
*
1.5
1.5
0.8
2.5
*
tolerance expires on October 6, 2021.
*
*
*
*
[FR Doc. 2021–06271 Filed 4–2–21; 8:45 am]
BILLING CODE 6560–50–P
SURFACE TRANSPORTATION BOARD
49 CFR Part 1201
[Docket No. EP 763]
Montana Rail Link, Inc.—Petition for
Rulemaking—Classification of Carriers
Surface Transportation Board.
Final rule.
AGENCY:
ACTION:
The Surface Transportation
Board (STB or Board) is adopting a final
rule amending the thresholds for
classifying rail carriers.
DATES: The rule is effective June 4, 2021.
FOR FURTHER INFORMATION CONTACT:
Amy Ziehm at (202) 245–0391.
Assistance for the hearing impaired is
available through the Federal Relay
Service at (800) 877–8339.
SUPPLEMENTARY INFORMATION: Under 49
CFR part 1201, General Instructions
section 1–1(a), rail carriers are grouped
into one of three classes for purposes of
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SUMMARY:
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accounting and reporting.1 The Board’s
classification of rail carriers affects the
degree to which they must file annual,
quarterly, and other operational reports,
see, e.g., 49 CFR pt. 1243 and also is
used in a variety of other contexts,
including differentiating the legal
standards and procedures that apply to
certain transactions subject to Board
licensing, see, e.g., 49 U.S.C. 10902,
11324, 11325, and prescribing labor
protection conditions, see, e.g., 49
U.S.C. 10903(b)(2), 11326, among
others.
The class to which any rail carrier
belongs is determined by its annual
operating revenues after application of a
revenue deflator adjustment. 49 CFR pt.
1201, section 1–1(b)(1). Currently, Class
I carriers have annual operating
revenues of $504,803,294 or more, Class
II carriers have annual operating
revenues of less than $504,803,294 and
more than $40,384,263, and Class III
carriers have annual operating revenues
of $40,384,263 or less, all when adjusted
for inflation. Section 1–1(a) (setting
thresholds unadjusted for inflation);
Indexing the Annual Operating
Revenues of R.Rs., EP 748 (STB served
June 10, 2020) (calculating revenue
deflator factor and publishing
thresholds adjusted for inflation based
on 2019 data).2 The revenue
classification levels for railroads set
forth at 49 CFR part 1201, General
Instructions section 1–1(a) were adopted
in 1992 by the Board’s predecessor, the
Interstate Commerce Commission, in the
1992 Rulemaking.
1 The agency ‘‘has broad discretion to require rail
carriers to report financial and operating data, and
to prescribe an underlying accounting system to
produce that information.’’ Mont. Rail Link, Inc. &
Wis. Cent. Ltd., Joint Pet. for Rulemaking with
Respect to 49 CFR part 1201 (1992 Rulemaking), 8
I.C.C.2d 625, 631 (1992); see also 49 U.S.C. 11144,
11145, 11161–64.
2 Instruction section 1–1(a) currently defines
Class I carriers as those with annual operating
revenues (in Year 1991 dollars) of $250 million or
more. To prevent this threshold from being
influenced by the effects of inflation, each year the
STB calculates a ‘‘deflator’’ factor that converts the
value of today’s dollar into its equivalent 1991
value. This deflator factor is then applied to a
carrier’s current revenues and the result is
compared to the $250 million threshold. The
railroad revenue deflator formula, which is based
on the Railroad Freight Price Index developed by
the Bureau of Labor Statistics, is as follows: Current
Year’s Revenues × (1991 Average Index/Current
Year’s Average Index). 49 CFR pt. 1201, section 1–
1 Note A. The Board publishes annually an updated
deflator factor. In addition, the Board applies the
reciprocal of the deflator factor to identify where
the $250 million threshold lies expressed in current
dollars. The current Class I revenue threshold, as
noted above, corresponds to $504,803,294 in 2019
dollars. The Class II/Class III threshold, which is
listed in Instruction section 1–1(a) as $20 million,
corresponds to $40,384,263 in 2019 dollars.
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Background
On February 14, 2020, Montana Rail
Link, Inc. (MRL), filed a petition for
rulemaking to amend the Board’s rail
carrier classification regulations. In its
petition, MRL requested that the Board
increase the revenue threshold for Class
I carriers to $900 million. (Pet. 1.) MRL
contended that it continues to be a
regional carrier operationally and
economically but may exceed the Class
I revenue threshold within two years.
(Id.) Citing principles drawn from the
1992 Rulemaking, in which the revenue
thresholds were last raised, MRL asked
that the Board address ‘‘whether a
regional carrier such as MRL should be
treated as a Class I carrier, taking into
account (1) the financial and operational
differences between MRL and existing
Class I carriers, and (2) the cost-benefit
analysis of imposing Class I
requirements on MRL.’’ (Id. at 12.)
MRL submitted eight letters in
support of its petition.3 No replies to
MRL’s petition were received.
On May 14, 2020, the Board initiated
a rulemaking proceeding to consider
MRL’s petition and consider issues
related to the Class I carrier revenue
threshold determination. The Board
invited ‘‘comment about whether it
should amend 49 CFR part 1201,
General Instructions section 1–1(a), to
increase the revenue threshold for Class
I carriers, and, if so, whether $900
million or another amount would be
appropriate.’’ Mont. Rail Link, Inc.—Pet.
for Rulemaking—Classification of
Carriers, EP 763, slip op. at 2 (STB
served May 14, 2020).
The Board received two comments in
response to its May 14, 2020 decision.
On June 15, 2020, the American Short
Line and Regional Railroad Association
(ASLRRA) filed in support of MRL’s
petition, arguing, among other things,
that Class II carriers such as MRL are
distinctly different from Class I carriers
and should continue to be classified in
their current category. (ASLRRA
Comment 2–4, June 15, 2020.) ASLRRA
stated that there is a ‘‘massive’’ revenue
gap between the largest Class II and the
smallest Class I carrier, (id. at 3), and
that the accounting, financial, and other
burdens imposed on a Class II carrier by
becoming a Class I carrier would
outweigh any resulting benefits, (id. at
2–4). Also on June 15, 2020, the
Transportation Trades Department,
AFL–CIO (TTD), a coalition of 33
3 Letters of support were from the Montana
Contractors’ Association, Montana Agricultural
Business Association, Montana Grain Elevator
Association, Montana Petroleum Association, Inc.,
Montana Taxpayers Association, Montana Chamber
of Commerce, Treasure State Resources Association,
and Montana Wood Products Association.
E:\FR\FM\05APR1.SGM
05APR1
Agencies
[Federal Register Volume 86, Number 63 (Monday, April 5, 2021)]
[Rules and Regulations]
[Pages 17545-17548]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2021-06271]
-----------------------------------------------------------------------
ENVIRONMENTAL PROTECTION AGENCY
40 CFR Part 180
[EPA-HQ-OPP-2020-0335; FRL-10019-55]
Pyriofenone; Pesticide Tolerances
AGENCY: Environmental Protection Agency (EPA).
ACTION: Final rule.
-----------------------------------------------------------------------
SUMMARY: This regulation establishes tolerances for residues of
pyriofenone in or on fruit, small vine climbing subgroup 13-07E, except
grape; grape and grape, raisin. ISK BIOSCIENCES Corporation requested
these tolerances under the Federal Food, Drug, and Cosmetic Act
(FFDCA).
DATES: This regulation is effective April 5, 2021. Objections and
requests for hearings must be received on or before May 5, 2021, and
must be filed in accordance with the instructions provided in 40 CFR
part 178 (see also Unit I.C. of the SUPPLEMENTARY INFORMATION).
ADDRESSES: The docket for this action, identified by docket
identification (ID) number EPA-HQ-OPP-2020-0335, 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.
Due to the public health concerns related to COVID-19, the EPA
Docket Center (EPA/DC) and Reading Room is closed to visitors with
limited exceptions. The staff continues to provide remote customer
service via email, phone, and webform. For the latest status
information on EPA/DC services and docket access, visit https://www.epa.gov/dockets.
FOR FURTHER INFORMATION CONTACT: Marietta Echeverria, Registration
Division (7505P), 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 EPA's
tolerance regulations at 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. To access the OCSPP
test guidelines referenced in this document electronically, please go
to https://www.epa.gov/ocspp and select ``Test Methods and Guidelines.''
C. How can I file an objection or hearing request?
Under FFDCA section 408(g), 21 U.S.C. 346a, 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-2020-0335 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
June 4, 2021. 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-2020-0335, 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
[[Page 17546]]
dockets generally, is available at https://www.epa.gov/dockets.
II. Summary of Petitioned-For Tolerance
In the Federal Register of August 5, 2020 (85 FR 47330) (FRL-10012-
32), EPA issued a document pursuant to FFDCA section 408(d)(3), 21
U.S.C. 346a(d)(3), announcing the filing of a pesticide petition (PP
9F8808) by ISK BIOSCIENCES Corporation, 7470 Auburn Road, Suite A,
Concord, OH, 44077. The petition requested that 40 CFR 180.660 be
amended by establishing tolerances for residues of the fungicide,
pyriofenone, (5-chloro-2-methoxy-4-methyl-3-pyridinyl)(2,3,4-
trimethoxy-6-methylphenyl) methanone, in or on fruit, small vine
climbing subgroup 13-07E, except grape at 1.5 parts per million (ppm);
grape at 0.8 ppm; and grape, raisin at 2.5 ppm. In addition, although
not mentioned in EPA's document, ISK's petition also requested that the
currently established tolerances for residues of pyriofenone in/on
fruit, small vine climbing subgroup 13-07D at 1.5 ppm be removed from
40 CFR 180.660, as establishment of the requested tolerances for
subgroup 13-07E and grape include all the crops in subgroup 13-07D.
That document referenced a summary of the petition prepared by ISK
BIOSCIENCES Corporation, the registrant, which is available in the
docket, https://www.regulations.gov. No comment was received in response
to the notice of filing.
III. Aggregate Risk Assessment and Determination of Safety
Section 408(b)(2)(A)(i) of FFDCA allows EPA to establish a
tolerance (the legal limit for a pesticide chemical residue in or on a
food) only if EPA determines that the tolerance is ``safe.'' Section
408(b)(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.
Section 408(b)(2)(C) of FFDCA requires EPA to give special
consideration to exposure of infants and children to the pesticide
chemical residue in establishing a tolerance 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. . .
.''
Consistent with FFDCA section 408(b)(2)(D), and the factors
specified in FFDCA section 408(b)(2)(D), EPA has reviewed the available
scientific data and other relevant information in support of this
action. EPA has sufficient data to assess the hazards of and to make a
determination on aggregate exposure for pyriofenone including exposure
resulting from the tolerances established by this action. EPA's
assessment of exposures and risks associated with pyriofenone follows.
In an effort to streamline its publications in the Federal
Register, EPA is not reprinting sections that repeat what has been
previously published for tolerance rulemakings of the same pesticide
chemical. Where scientific information concerning a particular chemical
remains unchanged, the content of those sections would not vary between
tolerance rulemakings, and republishing the same sections is
unnecessary; therefore, EPA considers referral back to those sections
as sufficient to provide an explanation of the information EPA
considered in making its safety determination for the new rulemaking.
EPA has previously published a number of tolerance rulemakings for
pyriofenone, in which EPA concluded, based on the available
information, that there is a reasonable certainty that no harm would
result from aggregate exposure to pyriofenone and established
tolerances for residues of that chemical. EPA is incorporating
previously published sections from those rulemakings as described
further in this rulemaking, as they remain unchanged.
Toxicological Profile. For a discussion of the Toxicological
Profile of pyriofenone, see Unit III.A. of the May 30, 2019 rulemaking
(84 FR 24983) (FRL-9993-11).
Toxicological Points of Departure/Levels of Concern. For a summary
of the Toxicological Points of Departure/Levels of Concern used for the
safety assessment, see Unit III.B. of the May 30, 2019 rulemaking.
Exposure Assessment. EPA's exposure assessment remains unchanged
from what was done in support of the May 30, 2019 rulemaking. EPA's
aggregate exposure assessments include exposures from food, drinking
water and residential sources, and there have been no changes since the
last assessment. For a discussion of EPA's assessment of aggregate
exposures, see Unit III.C. of the May 30, 2019 rulemaking.
Safety Factor for Infants and Children. EPA continues to conclude
that there is reliable data showing that the safety of infants and
children would be adequately protected if the FQPA SF were reduced from
10X to 1X for all exposure scenarios. The reasons for that decision are
articulated in Unit III.D. of the May 30, 2019 rulemaking.
Aggregate Risks and Determination of Safety. EPA determines whether
acute and chronic dietary pesticide exposures are safe by comparing
aggregate exposure estimates to the acute PAD (aPAD) and chronic PAD
(cPAD). Short-, intermediate-, and chronic-term risks are evaluated by
comparing the estimated aggregate food, water, and residential exposure
to the appropriate PODs to ensure that an adequate MOE exists. For
linear cancer risks, EPA calculates the lifetime probability of
acquiring cancer given the estimated aggregate exposure.
Pyriofenone is not expected to pose an acute risk, due to the lack
of acute adverse effects in the database. Chronic dietary risks are
below the Agency's level of concern: 6.9% of the chronic population
adjusted dose (cPAD) for children 1 to 2 years old, the group with the
highest exposure. There are no residential uses for pyriofenone;
therefore, the chronic aggregate risk is limited to the chronic dietary
risk and is not of concern. Short- and intermediate-term aggregate
risks are addressed by the chronic aggregate risk estimates and are not
a concern.
Therefore, based on the risk assessments and information described
above, EPA concludes there is a reasonable certainty that no harm will
result to the general populations, or to infants and children for
aggregate exposure to pyriofenone residues. More detailed information
on the subject action can be found at https://www.regulations.gov in
the document entitled, ``Pyriofenone. Human Health Risk Assessment for
the Section 3 Registration on Fruiting Vegetables (Crop Group 8-10)''
in the docket ID number EPA-HQ-OPP-2020-0335 and the document titled,
``Pyriofenone. Human Health Risk Assessment for the Section 3
Registration on Fruiting Vegetables (Crop Group 8-10)'' in docket ID
number EPA-HQ-OPP-2018-0677.
IV. Other Considerations
A. Analytical Enforcement Methodology
For a discussion of the available analytical enforcement method,
see Unit IV.A. of the May 30, 2019 rulemaking.
B. International Residue Limits
In making its tolerance decisions, EPA seeks to harmonize U.S.
tolerances with international standards whenever possible, consistent
with U.S. food safety standards and agricultural
[[Page 17547]]
practices. EPA considers the international maximum residue limits
(MRLs) established by the Codex Alimentarius Commission (Codex), as
required by FFDCA section 408(b)(4). The Codex Alimentarius is a joint
United Nations Food and Agriculture Organization/World Health
Organization food standards program, and it is recognized as an
international food safety standards-setting organization in trade
agreements to which the United States is a party. EPA may establish a
tolerance that is different from a Codex MRL; however, FFDCA section
408(b)(4) requires that EPA explain the reasons for departing from the
Codex level.
The Codex has established MRLs for pyriofenone in or on grape at
0.8 ppm and grape, raisin at 2.5 ppm. The U.S. tolerances for these
commodities are harmonized with these MRLs.
C. Revisions to Petitioned-For Tolerances
Under FFDCA section 408(d)(4)(A)(i), EPA may establish tolerances
that vary from those sought by the petition. The tolerance level has
been modified to be consistent with the Agency's rounding class
practices.
D. International Trade Considerations
In this Final Rule, EPA is establishing an individual tolerance for
grape at 0.8 ppm, which is lower than the current allowed amount of
residue on grape, by virtue of its inclusion in the small vine climbing
fruit subgroup 13-07D at 1.5 ppm. The Agency is reducing this tolerance
to harmonize with the Codex MRL on grape, and available residue data
demonstrate that this tolerance is sufficient to cover residues on this
commodity.
In accordance with the World Trade Organization's (WTO) Sanitary
and Phytosanitary Measures (SPS) Agreement, EPA intends to notify the
WTO of this revision. In addition, the SPS Agreement requires that
Members provide a ``reasonable interval'' between the publication of a
regulation subject to the Agreement and its entry into force to allow
time for producers in exporting Member countries to adapt to the new
requirement. To accommodate this reasonable interval, EPA is
establishing an expiration date for the existing tolerance for small
vine climbing fruit subgroup 13-07D to allow those tolerances to remain
in effect for a period of 6 months after the effective date of this
rule. At the end of that 6-month period, the existing tolerances for
subgroup 13-07D will no longer be valid; residues on grape will need to
comply with the new grape tolerance and residues on other commodities
in that subgroup will need to comply with the new subgroup 13-07E
tolerance.
This reduction in tolerance level is not discriminatory; the same
food safety standard contained in the FFDCA applies equally to
domestically produced and imported foods. The new tolerance level is
supported by available residue data.
V. Conclusion
Therefore, tolerances are established for residues of pyriofenone,
(5-chloro-2-methoxy-4-methyl-3-pyridinyl)(2,3,4-trimethoxy-6-
methylphenyl) methanone, in or on fruit, small vine climbing subgroup
13-07E, except grape at 1.5 ppm; grape at 0.8 ppm; and grape, raisin at
2.5 ppm. EPA is also establishing an expiration date for the existing
tolerance for fruit, small vine climbing subgroup 13-07D.
VI. Statutory and Executive Order Reviews
This action establishes and modifies tolerances under FFDCA section
408(d) in response to a petition submitted to the Agency. 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 considered 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 in this
final rule, 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, nor does this
action alter the relationships or distribution of power and
responsibilities established by Congress in the preemption provisions
of FFDCA section 408(n)(4). As such, the Agency 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, the Agency 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 Agency 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).
VII. 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: March 8, 2021.
Marietta Echeverria,
Acting Director, Registration Division, Office of Pesticide Programs.
Therefore, for the reasons stated in the preamble, EPA is amending
40 CFR chapter I as follows:
[[Page 17548]]
PART 180--TOLERANCES AND EXEMPTIONS FOR PESTICIDE CHEMICAL RESIDUES
IN FOOD
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. In Sec. 180.660, amend the table in paragraph (a) by:
0
a. Designating the table as Table 1;
0
b. Revising the entry for ``Fruit, small vine climbing, subgroup 13-
07D''; and
0
c. Adding in alphabetical order entries for ``Fruit, small vine
climbing, subgroup 13-07E, except grape''; ``Grape''; and ``Grape,
raisin''.
The additions and revision read as follows:
Sec. 180.660 Pyriofenone; tolerances for residues.
* * * * *
Table 1 to Paragraph (a)
------------------------------------------------------------------------
Parts
Commodity per
million
------------------------------------------------------------------------
* * * * *
Fruit, small vine climbing subgroup 13-07D \1\................ 1.5
Fruit, small vine climbing subgroup 13-07E, except grape...... 1.5
Grape......................................................... 0.8
Grape, raisin................................................. 2.5
* * * * *
------------------------------------------------------------------------
\1\ This tolerance expires on October 6, 2021.
* * * * *
[FR Doc. 2021-06271 Filed 4-2-21; 8:45 am]
BILLING CODE 6560-50-P