Trifluralin; Pesticide Tolerance, 21641-21644 [05-8384]
Download as PDF
Federal Register / Vol. 70, No. 80 / Wednesday, April 27, 2005 / Rules and Regulations
Parts per
million
Commodity
Sheep, meat byproducts ..........
0.05
(b) Section 18 emergency exemptions.
[Reserved]
(c) Tolerances with regional
registrations. [Reserved]
(d) Indirect or inadvertent residues.
[Reserved]
[FR Doc. 05–8120 Filed 4–26–05; 8:45 am]
BILLING CODE 6560–50–S
through Friday, excluding legal
holidays. The docket telephone number
is (703) 305–5805.
John
W. Pates, Jr., Special Review and
Reregistration Division (7508C), Office
of Pesticide Programs, Environmental
Protection Agency, 1200 Pennsylvania
Ave., NW., Washington, DC 20460–
0001; telephone number: 703–308–8195;
e-mail address: pates.john@epa.gov.
FOR FURTHER INFORMATION CONTACT:
SUPPLEMENTARY INFORMATION:
I. General Information
A. Does this Action Apply to Me?
ENVIRONMENTAL PROTECTION
AGENCY
40 CFR Part 180
[OPP–2004–0142; FRL–7710–9]
Trifluralin; Pesticide Tolerance
Environmental Protection
Agency (EPA).
ACTION: Final rule.
AGENCY:
SUMMARY: This regulation establishes a
tolerance for residues of trifluralin in
spearmint and peppermint oil under the
Federal Food, Drug, and Cosmetic Act
(FFDCA), as amended by the Food
Quality Protection Act of 1996 (FQPA).
The FQPA substantially rewrote section
408 of FFDCA. As a result, the revisions
made it necessary, once again, to
establish tolerances for mint oils that
had previously been deemed
unnecessary.
This regulation is effective April
27, 2005. Objections and requests for
hearings must be received on or before
June 27, 2005.
ADDRESSES: To submit a written
objection or hearing request follow the
detailed instructions as provided in
Unit VI. of the SUPPLEMENTARY
INFORMATION. EPA has established a
docket for this action under Docket
identification (ID) number OPP–2004–
0142. All documents in the docket are
listed in the EDOCKET index at http:/
/www.epa.gov/edocket. Although listed
in the index, some information is not
publicly available, i.e., CBI or other
information whose disclosure is
restricted by statute. Certain other
material, such as copyrighted material,
is not placed on the Internet and will be
publicly available only in hard copy
form. Publicly available docket
materials are available either
electronically in EDOCKET or in hard
copy at the Public Information and
Records Integrity Branch (PIRIB), Rm.
119, Crystal Mall #2, 1801 S. Bell St.,
Arlington, VA. This docket facility is
open from 8:30 a.m. to 4 p.m., Monday
DATES:
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You may be potentially affected by
this action if you are an agricultural
producer, food manufacturer, or
pesticide manufacturer. Potentially
affected entities may include, but are
not limited to:
• Crop production (NAICS 111), e.g.,
agricultural workers; greenhouse,
nursery, and floriculture workers;
farmers.
• Animal production (NAICS 112),
e.g., cattle ranchers and farmers, dairy
cattle farmers, livestock farmers.
• Food manufacturing (NAICS 311),
e.g., agricultural workers; farmers;
greenhouse, nursery, and floriculture
workers; ranchers; pesticide applicators.
• Pesticide manufacturing (NAICS
32532), e.g., agricultural workers;
commercial applicators; farmers;
greenhouse, nursery, and floriculture
workers; residential users.
This listing is not intended to be
exhaustive, but rather provides a guide
for readers regarding entities likely to be
affected by this action. Other types of
entities not listed in this unit could also
be affected. The North American
Industrial Classification System
(NAICS) codes have been provided to
assist you and others in determining
whether this action might apply to
certain entities. If you have any
questions regarding the applicability of
this action to a particular entity, consult
the person listed under FOR FURTHER
INFORMATION CONTACT.
B. How Can I Access Electronic Copies
of this Document and Other Related
Information?
In addition to using EDOCKET (http:/
/www.epa.gov/edocket/), you may
access this Federal Register document
electronically through the EPA Internet
under the ‘‘Federal Register’’ listings at
https://www.epa.gov/fedrgstr/. A
frequently updated electronic version of
40 CFR part 180 is available at E-CFR
Beta Site Two at https://
www.gpoaccess.gov/ecfr/.
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21641
II. Background
In the Federal Register of November
24, 2004 (69 FR 68287) (FRL–7686–4),
EPA on its own initiative, under section
408(e) of FFDCA, 21 U.S.C. 346a(e),
announced a proposal to establish a
permanent tolerance for residues of the
herbicide trifluralin in spearmint and
peppermint oil at 2.0 parts per million
(ppm). The proposal included a
summary of the exposure assessment
prepared by the Agency. The Agency
received three submissions for
comment; two from private citizens and
one from Dow AgroSciences, the
registrant.
III. Response to Comments
Comments received from the
registrant address the following areas:
evidence of errors and inconsistencies/
miscalculations, belief that potential
risks are significantly overstated, belief
that unrealistic assumptions have been
made, and the position that relevant
information has been omitted and not
incorporated into the Agency’s
decision(s). Additionally, the registrant
has asked for clarification on labeling
requirements. However, in general, the
registrant does agree with the
assessments that have been conducted
for the human health and residue
chemistry risk studies available for
trifluralin. Furthermore, the registrant
does not state any objections to the
establishment of a permanent tolerance
for residues of the herbicide trifluralin
in peppermint and spearmint oil at 2.0
ppm.
One of the private citizen’s comments
raised objections to any establishment of
a tolerance for trifluralin. The citizen’s
comments and EPA’s response to those
comments follow:
1. Comment. Both 28–day dermal and
developmental toxicity tests on rabbits
as well as a 1–year oral capsule study
on dogs have no validity and are
abusive to the test animals.
EPA response. This commenter’s
objections to animal testing have been
addressed in prior rulemaking
documents. See 69 FR 63083, 63096
(October 29, 2004).
2. Comment. 1994 surveys of food
intake are out of date.
EPA response. Consumption survey
data is used in part to determine acute
and chronic exposure. In assessing
exposure to trifluralin, EPA relied on
food consumption data as reported by
respondents in the United States
Department of Agriculture (USDA)
1994–1996 and 1998 Nationwide
Continuing Surveys of Food Intake by
Individuals (CSFII). These surveys are
generally updated every 10 years or so.
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The commenter claims the USDA
surveys are out of date. The basis for
this assertion is the commenter’s
observation that Americans are obese.
This type of unsupported allegation is
insufficient to call into question EPA’s
reliance on scientifically-designed
studies. In any event, EPA’s experience
has been that while eating patterns
change over time, these changes are
generally marginal between surveys.
3. Comment. The DEEM software is
not suitable for evaluating exposure/risk
EPA response. The commenter
provides no basis for claiming that the
DEEM is unsuitable for risk assessment.
For this reason alone, the comment is
insignificant. EPA would note, however,
that the DEEM software has been
thoroughly tested by the Agency and
has been reviewed by an independent
body of technical experts, the FIFRA
Scientific Advisory Panel, and found to
be suitable for evaluating risks of
pesticide residues on food. The results
of that review may be found at https://
www.epa.gov/scipoly/sap/2000/
february/
partialfinalreport06292000.pdf.
4. Comment. Exposure to residential
handlers makes the product too
dangerous to be sold.
EPA response. The commenter states
that if there are any exposures to
residential handlers, then the product is
far too dangerous to use or be sold. In
response, EPA would first note that this
tolerance rulemaking is being conducted
under the FFDCA, and EPA does not
regulate the sale or use of pesticides in
residential settings under the FFDCA,
although EPA does consider exposure
from residential uses of pesticides in
determining whether pesticide
tolerances are safe. Decisions on
whether a pesticide may be sold and
distributed for residential uses is made
pursuant to the Federal Insecticide,
Fungicide, and Rodenticide Act
(FIFRA), 7 U.S.C. 136 et seq. Based on
its uses, trifluralin has been assessed
under the FFDCA for the residential
applicator as well as other potential
contact sources. Residential exposure
scenarios were developed based on the
use sites, formulations, application
rates, and the various other equipment
that could be used during applications.
Residential risk estimates are also based
on estimates (and assumptions)
regarding the body weight of a typical
homeowner/applicator, the area treated
per application, and the seasonal
duration (in days) of exposure. It is also
assumed that residential applicators
complete all elements of an application
(mix/load/apply) without use of
protective equipment (assessments are
based on an assumption that individuals
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will be wearing short-sleeved shirts and
short pants). For short-term non-cancer
risks to residential handlers, a margin of
exposure (MOE) of less than 100
exceeds the Agency’s level of concern.
For residential handlers, calculations of
short-term inhalation non-cancer risk
indicate that the MOEs are greater than
100 for all residential handler scenarios.
Likewise, residential handler cancer risk
indicates that all scenarios are below the
Agency’s level of concern. Therefore,
the Agency is confident that no
unreasonable risk exists (excluding any
misuse) based on the assumptions
made, likely scenarios, and the
conservative approach used in
determining any potential risk problem
for residential handlers.
Another private citizen objected to
allowing this genetically-modified crop
to become a legal use in the United
States or anywhere else. The commenter
argued that genetic modification of
plants is an unknown danger to humans
as well as a wide variety of other
species. In response, EPA would note
that the commenter is mistaken in
concluding that the production of
trifluralin involves genetic modification
of plants.
IV. Conclusion
Based on the information, analysis,
and conclusions in the November 24,
2004 (69 FR 68287) proposal, a
tolerance is established for residues of
trifluralin, alpha, alpha, alpha-trifluoro2,6-dinitro-N,N-dipropyl-p-toluidine, in
or on spearmint and peppermint oil at
2.0 ppm.
V. Objections and Hearing Requests
Under section 408(g) of FFDCA, as
amended by FQPA, any person may file
an objection to any aspect of this
regulation and may also request a
hearing on those objections. The EPA
procedural regulations which govern the
submission of objections and requests
for hearings appear in 40 CFR part 178.
Although the procedures in those
regulations require some modification to
reflect the amendments made to FFDCA
by FQPA, EPA will continue to use
those procedures, with appropriate
adjustments, until the necessary
modifications can be made. The new
section 408(g) of FFDCA provides
essentially the same process for persons
to ‘‘object’’ to a regulation for an
exemption from the requirement of a
tolerance issued by EPA under new
section 408(d) of FFDCA, as was
provided in the old sections 408 and
409 of FFDCA. However, the period for
filing objections is now 60 days, rather
than 30 days.
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A. What Do I Need to Do to File an
Objection or Request a Hearing?
You must file your objection or
request a hearing on this regulation in
accordance with the instructions
provided in this unit and in 40 CFR part
178. To ensure proper receipt by EPA,
you must identify docket ID number
OPP–2004–0142 in the subject line on
the first page of your submission. All
requests must be in writing, and must be
mailed or delivered to the Hearing Clerk
on or before June 27, 2005.
1. Filing the request. Your objection
must specify the specific provisions in
the regulation that you object to, and the
grounds for the objections (40 CFR
178.25). If a hearing is requested, the
objections must include a statement of
the factual issues(s) on which a hearing
is requested, the requestor’s contentions
on such issues, and a summary of any
evidence relied upon by the objector (40
CFR 178.27). Information submitted in
connection with an objection or hearing
request may be claimed confidential by
marking any part or all of that
information as CBI. Information so
marked will not be disclosed except in
accordance with procedures set forth in
40 CFR part 2. A copy of the
information that does not contain CBI
must be submitted for inclusion in the
public record. Information not marked
confidential may be disclosed publicly
by EPA without prior notice.
Mail your written request to: Office of
the Hearing Clerk (1900L),
Environmental Protection Agency, 1200
Pennsylvania Ave., NW., Washington,
DC 20460–0001. You may also deliver
your request to the Office of the Hearing
Clerk in Suite 350, 1099 14th St., NW.,
Washington, DC 20005. The Office of
the Hearing Clerk is open from 8 a.m.
to 4 p.m., Monday through Friday,
excluding legal holidays. The telephone
number for the Office of the Hearing
Clerk is (202) 564–6255.
2. Copies for the Docket. In addition
to filing an objection or hearing request
with the Hearing Clerk as described in
Unit V.A., you should also send a copy
of your request to the PIRIB for its
inclusion in the official record that is
described in ADDRESSES. Mail your
copies, identified by docket ID number
OPP–2004–0142, to: Public Information
and Records Integrity Branch,
Information Resources and Services
Division (7502C), Office of Pesticide
Programs, Environmental Protection
Agency, 1200 Pennsylvania Ave., NW.,
Washington, DC 20460–0001. In person
or by courier, bring a copy to the
location of the PIRIB described in
ADDRESSES. You may also send an
electronic copy of your request via e-
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mail to: opp-docket@epa.gov. Please use
an ASCII file format and avoid the use
of special characters and any form of
encryption. Copies of electronic
objections and hearing requests will also
be accepted on disks in WordPerfect
6.1/8.0 or ASCII file format. Do not
include any CBI in your electronic copy.
You may also submit an electronic copy
of your request at many Federal
Depository Libraries.
B. When Will the Agency Grant a
Request for a Hearing?
A request for a hearing will be granted
if the Administrator determines that the
material submitted shows the following:
There is a genuine and substantial issue
of fact; there is a reasonable possibility
that available evidence identified by the
requestor would, if established resolve
one or more of such issues in favor of
the requestor, taking into account
uncontested claims or facts to the
contrary; and resolution of the factual
issues(s) in the manner sought by the
requestor would be adequate to justify
the action requested (40 CFR 178.32).
VI. Statutory and Executive Order
Reviews
This final rule establishes a tolerance
under section 408(d) of FFDCA on
EPA’s own initiaive. 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 rule has been exempted
from review under Executive Order
12866 due to its lack of significance,
this rule is not subject to Executive
Order 13211, Actions Concerning
Regulations That Significantly Affect
Energy Supply, Distribution, or Use (66
FR 28355, May 22, 2001). This final rule
does not contain any information
collections subject to OMB approval
under the Paperwork Reduction Act
(PRA), 44 U.S.C. 3501 et seq., or impose
any enforceable duty or contain any
unfunded mandate as described under
Title II of the Unfunded Mandates
Reform Act of 1995 (UMRA) (Public
Law 104–4). 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); or OMB review or any Agency
action under Executive Order 13045,
entitled Protection of Children from
Environmental Health Risks and Safety
Risks (62 FR 19885, April 23, 1997).
This action does not involve any
technical standards that would require
Agency consideration of voluntary
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consensus standards pursuant to section
12(d) of the National Technology
Transfer and Advancement Act of 1995
(NTTAA), Public Law 104–113, section
12(d) (15 U.S.C. 272 note). Pursuant to
the requirements of the Regulatory
Flexibility Act (RFA) (5 U.S.C. 601 et
seq.), the Agency hereby certifies that
this rule will not have significant
negative economic impact on a
substantial number of small entities. In
addition, the Agency has determined
that this action will not have a
substantial direct effect on States, on the
relationship between the national
government and the States, or on the
distribution of power and
responsibilities among the various
levels of government, as specified in
Executive Order 13132, entitled
Federalism (64 FR 43255, August 10,
1999). Executive Order 13132 requires
EPA to develop an accountable process
to ensure ‘‘meaningful and timely input
by State and local officials in the
development of regulatory policies that
have federalism implications.’’ ‘‘Policies
that have federalism implications’’ is
defined in the Executive order to
include regulations that have
‘‘substantial direct effects on the States,
on the relationship between the national
government and the States, or on the
distribution of power and
responsibilities among the various
levels of government.’’ This final rule
directly regulates growers, food
processors, food handlers and food
retailers, not States. This action does not
alter the relationships or distribution of
power and responsibilities established
by Congress in the preemption
provisions of section 408(n)(4) of
FFDCA. For these same reasons, the
Agency has determined that this rule
does not have any ‘‘tribal implications’’
as described in Executive Order 13175,
entitled Consultation and Coordination
with Indian Tribal Governments (65 FR
67249, November 6, 2000). Executive
Order 13175, requires EPA to develop
an accountable process to ensure
‘‘meaningful and timely input by tribal
officials in the development of
regulatory policies that have tribal
implications.’’ ‘‘Policies that have tribal
implications’’ is defined in the
Executive order to include regulations
that have ‘‘substantial direct effects on
one or more Indian tribes, on the
relationship between the Federal
Government and the Indian tribes, or on
the distribution of power and
responsibilities between the Federal
Government and Indian tribes.’’ This
rule will not have substantial direct
effects on tribal governments, on the
relationship between the Federal
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Government and Indian tribes, or on the
distribution of power and
responsibilities between the Federal
Government and Indian tribes, as
specified in Executive Order 13175.
Thus, Executive Order 13175 does not
apply to this rule.
VII. Congressional Review Act
The Congressional Review Act, 5
U.S.C. 801 et seq., as added by the Small
Business Regulatory Enforcement
Fairness Act of 1996, generally provides
that before a rule may take effect, the
agency promulgating the rule must
submit a rule report, which includes a
copy of the rule, to each House of the
Congress and to the Comptroller General
of the United States. 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 this final
rule in the Federal Register. This final
rule 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: April 20, 2005.
Debra Edwards,
Director, Special Review and Reregistration
Division, Office of Pesticide Programs.
Therefore, 40 CFR chapter I is
amended as follows:
I
PART 180—[AMENDED]
1. The authority citation for part 180
continues to read as follows:
I
Authority: 21 U.S.C. 321(q), 346a and 371.
2. Section 180.207 is amended by
adding alphabetically entries for
‘‘peppermint oil,’’ and ‘‘spearmint oil’’ to
the table in paragraph (a). For the
convenience of the reader the entire table
to paragraph (a) is shown below.
I
§ 180.207 Trifluralin; tolerances for
residues.
(a) *
*
*
Commodity
Alfalfa, hay ................................
Asparagus .................................
Barley, hay ................................
Barley, straw .............................
Bean, mung, sprouts ................
Carrot, roots ..............................
Corn, field, forage .....................
Corn, field, grain .......................
Corn, field, stover .....................
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1.0
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Parts per
million
Commodity
Cotton, undelinted seed ...........
Cress, upland ...........................
Flax, seed .................................
Fruit, citrus, group 10 ...............
Fruit, stone, group 12 ...............
Grain, crop, except corn, sweet
and rice grain ........................
Grape ........................................
Hop ...........................................
Legume, forage ........................
Nut, tree, group 14 ...................
Peanut ......................................
Peppermint oil ...........................
Peppermint, tops ......................
Rapeseed, seed .......................
Safflower, seed .........................
Sorghum, forage .......................
Sorghum, grain, stover .............
Spearmint oil .............................
Spearmint, tops ........................
Sugarcane, cane ......................
Sunflower, seed ........................
Vegetable, cucurbit, group 9 ....
Vegetable, fruiting, group 8 ......
Vegetables, leafy ......................
Vegetables, root (exc. carrots)
Vegetables, seed and pod .......
Wheat, grain .............................
Wheat, straw .............................
*
*
*
*
0.05
0.05
0.05
0.05
0.05
0.05
0.05
0.05
0.05
0.05
0.05
2.0
0.05
0.05
0.05
0.05
0.05
2.0
0.05
0.05
0.05
0.05
0.05
0.05
0.05
0.05
0.05
0.05
*
[FR Doc. 05–8384 Filed 4–26–05; 8:45 am]
BILLING CODE 6560–50–S
ENVIRONMENTAL PROTECTION
AGENCY
40 CFR Part 300
[FRL–7903–7]
National Priorities List for Uncontrolled
Hazardous Waste Sites
Environmental Protection
Agency.
ACTION: Final rule.
AGENCY:
SUMMARY: The Comprehensive
Environmental Response,
Compensation, and Liability Act of 1980
(‘‘CERCLA’’ or ‘‘the Act’’), as amended,
requires that the National Oil and
Hazardous Substances Pollution
Contingency Plan (‘‘NCP’’) include a list
of national priorities among the known
releases or threatened releases of
hazardous substances, pollutants, or
contaminants throughout the United
States. The National Priorities List
(‘‘NPL’’) constitutes this list. The NPL is
intended primarily to guide the
Environmental Protection Agency
(‘‘EPA’’ or ‘‘the Agency’’) in determining
which sites warrant further
investigation. These further
investigations will allow EPA to assess
the nature and extent of public health
and environmental risks associated with
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the site and to determine what CERCLAfinanced remedial action(s), if any, may
be appropriate. This rule adds ten new
sites to the General Superfund Section
of the NPL.
DATES: Effective Date: The effective date
for this amendment to the NCP shall be
May 27, 2005.
ADDRESSES: For addresses for the
Headquarters and Regional dockets, as
well as further details on what these
dockets contain, see section II,
‘‘Availability of Information to the
Public’’ in the SUPPLEMENTARY
INFORMATION portion of this preamble.
FOR FURTHER INFORMATION CONTACT:
Terry Jeng, phone (703) 603–8852, State,
Tribal and Site Identification Branch;
Assessment and Remediation Division;
Office of Superfund Remediation and
Technology Innovation (mail code
5204G); U.S. Environmental Protection
Agency; 1200 Pennsylvania Avenue,
NW.; Washington, DC 20460; or the
Superfund Hotline, phone (800) 424–
9346 or (703) 412–9810 in the
Washington, DC, metropolitan area.
SUPPLEMENTARY INFORMATION:
Table of Contents
I. Background
A. What are CERCLA and SARA?
B. What is the NCP?
C. What is the National Priorities List
(NPL)?
D. How are Sites Listed on the NPL?
E. What Happens to Sites on the NPL?
F. Does the NPL Define the Boundaries of
Sites?
G. How are Sites Removed from the NPL?
H. May EPA Delete Portions of Sites From
the NPL as They Are Cleaned Up?
I. What is the Construction Completion List
(CCL)?
II. Availability of Information to the Public
A. May I Review the Documents Relevant
to this Final Rule?
B. What Documents are Available for
Review at the Headquarters Docket?
C. What Documents are Available for
Review at the Regional Dockets?
D. How Do I Access the Documents?
E. How May I Obtain a Current List of NPL
Sites?
III. Contents of This Final Rule
A. Additions to the NPL
B. What did EPA Do with the Public
Comments It Received?
IV. Statutory and Executive Order Reviews
A. Executive Order 12866: Regulatory
Planning and Review
1. What is Executive Order 12866?
2. Is this Final Rule Subject to Executive
Order 12866 Review?
B. Paperwork Reduction Act
1. What is the Paperwork Reduction Act?
2. Does the Paperwork Reduction Act
Apply to This Final Rule?
C. Regulatory Flexibility Act
1. What is the Regulatory Flexibility Act?
2. How Has EPA Complied with the
Regulatory Flexibility Act?
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D. Unfunded Mandates Reform Act
1. What is the Unfunded Mandates Reform
Act (UMRA)?
2. Does UMRA Apply to This Final Rule?
E. Executive Order 13132: Federalism
1. What Is Executive Order 13132 and Is It
Applicable to This Final Rule?
F. Executive Order 13175: Consultation
and Coordination with Indian Tribal
Governments
1. What is Executive Order 13175?
2. Does Executive Order 13175 Apply to
This Final Rule?
G. Executive Order 13045: Protection of
Children from Environmental Health and
Safety Risks
1. What is Executive Order 13045?
2. Does Executive Order 13045 Apply to
This Final Rule?
H. Executive Order 13211
1. What is Executive Order 13211?
2. Is this Rule Subject to Executive Order
13211?
I. National Technology Transfer and
Advancement Act
1. What is the National Technology
Transfer and Advancement Act?
2. Does the National Technology Transfer
and Advancement Act Apply to this
Final Rule?
J. Possible Changes to the Effective Date of
the Rule
1. Has EPA Submitted This Rule to
Congress and the General Accounting
Office?
2. Could the Effective Date of This Final
Rule Change?
3. What Could Cause a Change in the
Effective Date of This Rule?
I. Background
A. What Are CERCLA and SARA?
In 1980, Congress enacted the
Comprehensive Environmental
Response, Compensation, and Liability
Act, 42 U.S.C. 9601–9675 (‘‘CERCLA’’ or
‘‘the Act’’), in response to the dangers of
uncontrolled releases or threatened
releases of hazardous substances, and
releases or substantial threats of releases
into the environment of any pollutant or
contaminant which may present an
imminent or substantial danger to the
public health or welfare. CERCLA was
amended on October 17, 1986, by the
Superfund Amendments and
Reauthorization Act (‘‘SARA’’), Public
Law 99–499, 100 Stat. 1613 et seq.
B. What Is the NCP?
To implement CERCLA, EPA
promulgated the revised National Oil
and Hazardous Substances Pollution
Contingency Plan (‘‘NCP’’), 40 CFR part
300, on July 16, 1982 (47 FR 31180),
pursuant to CERCLA section 105 and
Executive Order 12316 (46 FR 42237,
August 20, 1981). The NCP sets
guidelines and procedures for
responding to releases and threatened
releases of hazardous substances, or
releases or substantial threats of releases
E:\FR\FM\27APR1.SGM
27APR1
Agencies
[Federal Register Volume 70, Number 80 (Wednesday, April 27, 2005)]
[Rules and Regulations]
[Pages 21641-21644]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 05-8384]
-----------------------------------------------------------------------
ENVIRONMENTAL PROTECTION AGENCY
40 CFR Part 180
[OPP-2004-0142; FRL-7710-9]
Trifluralin; Pesticide Tolerance
AGENCY: Environmental Protection Agency (EPA).
ACTION: Final rule.
-----------------------------------------------------------------------
SUMMARY: This regulation establishes a tolerance for residues of
trifluralin in spearmint and peppermint oil under the Federal Food,
Drug, and Cosmetic Act (FFDCA), as amended by the Food Quality
Protection Act of 1996 (FQPA). The FQPA substantially rewrote section
408 of FFDCA. As a result, the revisions made it necessary, once again,
to establish tolerances for mint oils that had previously been deemed
unnecessary.
DATES: This regulation is effective April 27, 2005. Objections and
requests for hearings must be received on or before June 27, 2005.
ADDRESSES: To submit a written objection or hearing request follow the
detailed instructions as provided in Unit VI. of the SUPPLEMENTARY
INFORMATION. EPA has established a docket for this action under Docket
identification (ID) number OPP-2004-0142. All documents in the docket
are listed in the EDOCKET index at https://www.epa.gov/edocket. Although
listed in the index, some information is not publicly available, i.e.,
CBI or other information whose disclosure is restricted by statute.
Certain other material, such as copyrighted material, is not placed on
the Internet and will be publicly available only in hard copy form.
Publicly available docket materials are available either electronically
in EDOCKET or in hard copy at the Public Information and Records
Integrity Branch (PIRIB), Rm. 119, Crystal Mall 2, 1801 S.
Bell St., Arlington, VA. This docket facility is open from 8:30 a.m. to
4 p.m., Monday through Friday, excluding legal holidays. The docket
telephone number is (703) 305-5805.
FOR FURTHER INFORMATION CONTACT: John W. Pates, Jr., Special Review and
Reregistration Division (7508C), Office of Pesticide Programs,
Environmental Protection Agency, 1200 Pennsylvania Ave., NW.,
Washington, DC 20460-0001; telephone number: 703-308-8195; e-mail
address: pates.john@epa.gov.
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.
Potentially affected entities may include, but are not limited to:
Crop production (NAICS 111), e.g., agricultural workers;
greenhouse, nursery, and floriculture workers; farmers.
Animal production (NAICS 112), e.g., cattle ranchers and
farmers, dairy cattle farmers, livestock farmers.
Food manufacturing (NAICS 311), e.g., agricultural
workers; farmers; greenhouse, nursery, and floriculture workers;
ranchers; pesticide applicators.
Pesticide manufacturing (NAICS 32532), e.g., agricultural
workers; commercial applicators; farmers; greenhouse, nursery, and
floriculture workers; residential users.
This listing is not intended to be exhaustive, but rather provides
a guide for readers regarding entities likely to be affected by this
action. Other types of entities not listed in this unit could also be
affected. The North American Industrial Classification System (NAICS)
codes have been provided to assist you and others in determining
whether this action might apply to certain entities. If you have any
questions regarding the applicability of this action to a particular
entity, consult the person listed under FOR FURTHER INFORMATION
CONTACT.
B. How Can I Access Electronic Copies of this Document and Other
Related Information?
In addition to using EDOCKET (https://www.epa.gov/edocket/), you may
access this Federal Register document electronically through the EPA
Internet under the ``Federal Register'' listings at https://www.epa.gov/
fedrgstr/. A frequently updated electronic version of 40 CFR part 180
is available at E-CFR Beta Site Two at https://www.gpoaccess.gov/ecfr/.
II. Background
In the Federal Register of November 24, 2004 (69 FR 68287) (FRL-
7686-4), EPA on its own initiative, under section 408(e) of FFDCA, 21
U.S.C. 346a(e), announced a proposal to establish a permanent tolerance
for residues of the herbicide trifluralin in spearmint and peppermint
oil at 2.0 parts per million (ppm). The proposal included a summary of
the exposure assessment prepared by the Agency. The Agency received
three submissions for comment; two from private citizens and one from
Dow AgroSciences, the registrant.
III. Response to Comments
Comments received from the registrant address the following areas:
evidence of errors and inconsistencies/miscalculations, belief that
potential risks are significantly overstated, belief that unrealistic
assumptions have been made, and the position that relevant information
has been omitted and not incorporated into the Agency's decision(s).
Additionally, the registrant has asked for clarification on labeling
requirements. However, in general, the registrant does agree with the
assessments that have been conducted for the human health and residue
chemistry risk studies available for trifluralin. Furthermore, the
registrant does not state any objections to the establishment of a
permanent tolerance for residues of the herbicide trifluralin in
peppermint and spearmint oil at 2.0 ppm.
One of the private citizen's comments raised objections to any
establishment of a tolerance for trifluralin. The citizen's comments
and EPA's response to those comments follow:
1. Comment. Both 28-day dermal and developmental toxicity tests on
rabbits as well as a 1-year oral capsule study on dogs have no validity
and are abusive to the test animals.
EPA response. This commenter's objections to animal testing have
been addressed in prior rulemaking documents. See 69 FR 63083, 63096
(October 29, 2004).
2. Comment. 1994 surveys of food intake are out of date.
EPA response. Consumption survey data is used in part to determine
acute and chronic exposure. In assessing exposure to trifluralin, EPA
relied on food consumption data as reported by respondents in the
United States Department of Agriculture (USDA) 1994-1996 and 1998
Nationwide Continuing Surveys of Food Intake by Individuals (CSFII).
These surveys are generally updated every 10 years or so.
[[Page 21642]]
The commenter claims the USDA surveys are out of date. The basis for
this assertion is the commenter's observation that Americans are obese.
This type of unsupported allegation is insufficient to call into
question EPA's reliance on scientifically-designed studies. In any
event, EPA's experience has been that while eating patterns change over
time, these changes are generally marginal between surveys.
3. Comment. The DEEM software is not suitable for evaluating
exposure/risk
EPA response. The commenter provides no basis for claiming that the
DEEM is unsuitable for risk assessment. For this reason alone, the
comment is insignificant. EPA would note, however, that the DEEM
software has been thoroughly tested by the Agency and has been reviewed
by an independent body of technical experts, the FIFRA Scientific
Advisory Panel, and found to be suitable for evaluating risks of
pesticide residues on food. The results of that review may be found at
https://www.epa.gov/scipoly/sap/2000/february/
partialfinalreport06292000.pdf.
4. Comment. Exposure to residential handlers makes the product too
dangerous to be sold.
EPA response. The commenter states that if there are any exposures
to residential handlers, then the product is far too dangerous to use
or be sold. In response, EPA would first note that this tolerance
rulemaking is being conducted under the FFDCA, and EPA does not
regulate the sale or use of pesticides in residential settings under
the FFDCA, although EPA does consider exposure from residential uses of
pesticides in determining whether pesticide tolerances are safe.
Decisions on whether a pesticide may be sold and distributed for
residential uses is made pursuant to the Federal Insecticide,
Fungicide, and Rodenticide Act (FIFRA), 7 U.S.C. 136 et seq. Based on
its uses, trifluralin has been assessed under the FFDCA for the
residential applicator as well as other potential contact sources.
Residential exposure scenarios were developed based on the use sites,
formulations, application rates, and the various other equipment that
could be used during applications. Residential risk estimates are also
based on estimates (and assumptions) regarding the body weight of a
typical homeowner/applicator, the area treated per application, and the
seasonal duration (in days) of exposure. It is also assumed that
residential applicators complete all elements of an application (mix/
load/apply) without use of protective equipment (assessments are based
on an assumption that individuals will be wearing short-sleeved shirts
and short pants). For short-term non-cancer risks to residential
handlers, a margin of exposure (MOE) of less than 100 exceeds the
Agency's level of concern. For residential handlers, calculations of
short-term inhalation non-cancer risk indicate that the MOEs are
greater than 100 for all residential handler scenarios. Likewise,
residential handler cancer risk indicates that all scenarios are below
the Agency's level of concern. Therefore, the Agency is confident that
no unreasonable risk exists (excluding any misuse) based on the
assumptions made, likely scenarios, and the conservative approach used
in determining any potential risk problem for residential handlers.
Another private citizen objected to allowing this genetically-
modified crop to become a legal use in the United States or anywhere
else. The commenter argued that genetic modification of plants is an
unknown danger to humans as well as a wide variety of other species. In
response, EPA would note that the commenter is mistaken in concluding
that the production of trifluralin involves genetic modification of
plants.
IV. Conclusion
Based on the information, analysis, and conclusions in the November
24, 2004 (69 FR 68287) proposal, a tolerance is established for
residues of trifluralin, alpha, alpha, alpha-trifluoro-2,6-dinitro-N,N-
dipropyl-p-toluidine, in or on spearmint and peppermint oil at 2.0 ppm.
V. Objections and Hearing Requests
Under section 408(g) of FFDCA, as amended by FQPA, any person may
file an objection to any aspect of this regulation and may also request
a hearing on those objections. The EPA procedural regulations which
govern the submission of objections and requests for hearings appear in
40 CFR part 178. Although the procedures in those regulations require
some modification to reflect the amendments made to FFDCA by FQPA, EPA
will continue to use those procedures, with appropriate adjustments,
until the necessary modifications can be made. The new section 408(g)
of FFDCA provides essentially the same process for persons to
``object'' to a regulation for an exemption from the requirement of a
tolerance issued by EPA under new section 408(d) of FFDCA, as was
provided in the old sections 408 and 409 of FFDCA. However, the period
for filing objections is now 60 days, rather than 30 days.
A. What Do I Need to Do to File an Objection or Request a Hearing?
You must file your objection or request a hearing on this
regulation in accordance with the instructions provided in this unit
and in 40 CFR part 178. To ensure proper receipt by EPA, you must
identify docket ID number OPP-2004-0142 in the subject line on the
first page of your submission. All requests must be in writing, and
must be mailed or delivered to the Hearing Clerk on or before June 27,
2005.
1. Filing the request. Your objection must specify the specific
provisions in the regulation that you object to, and the grounds for
the objections (40 CFR 178.25). If a hearing is requested, the
objections must include a statement of the factual issues(s) on which a
hearing is requested, the requestor's contentions on such issues, and a
summary of any evidence relied upon by the objector (40 CFR 178.27).
Information submitted in connection with an objection or hearing
request may be claimed confidential by marking any part or all of that
information as CBI. Information so marked will not be disclosed except
in accordance with procedures set forth in 40 CFR part 2. A copy of the
information that does not contain CBI must be submitted for inclusion
in the public record. Information not marked confidential may be
disclosed publicly by EPA without prior notice.
Mail your written request to: Office of the Hearing Clerk (1900L),
Environmental Protection Agency, 1200 Pennsylvania Ave., NW.,
Washington, DC 20460-0001. You may also deliver your request to the
Office of the Hearing Clerk in Suite 350, 1099 14th St.,
NW., Washington, DC 20005. The Office of the Hearing Clerk is open from
8 a.m. to 4 p.m., Monday through Friday, excluding legal holidays. The
telephone number for the Office of the Hearing Clerk is (202) 564-6255.
2. Copies for the Docket. In addition to filing an objection or
hearing request with the Hearing Clerk as described in Unit V.A., you
should also send a copy of your request to the PIRIB for its inclusion
in the official record that is described in ADDRESSES. Mail your
copies, identified by docket ID number OPP-2004-0142, to: Public
Information and Records Integrity Branch, Information Resources and
Services Division (7502C), Office of Pesticide Programs, Environmental
Protection Agency, 1200 Pennsylvania Ave., NW., Washington, DC 20460-
0001. In person or by courier, bring a copy to the location of the
PIRIB described in ADDRESSES. You may also send an electronic copy of
your request via e-
[[Page 21643]]
mail to: opp-docket@epa.gov. Please use an ASCII file format and avoid
the use of special characters and any form of encryption. Copies of
electronic objections and hearing requests will also be accepted on
disks in WordPerfect 6.1/8.0 or ASCII file format. Do not include any
CBI in your electronic copy. You may also submit an electronic copy of
your request at many Federal Depository Libraries.
B. When Will the Agency Grant a Request for a Hearing?
A request for a hearing will be granted if the Administrator
determines that the material submitted shows the following: There is a
genuine and substantial issue of fact; there is a reasonable
possibility that available evidence identified by the requestor would,
if established resolve one or more of such issues in favor of the
requestor, taking into account uncontested claims or facts to the
contrary; and resolution of the factual issues(s) in the manner sought
by the requestor would be adequate to justify the action requested (40
CFR 178.32).
VI. Statutory and Executive Order Reviews
This final rule establishes a tolerance under section 408(d) of
FFDCA on EPA's own initiaive. 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 rule has been exempted from review under Executive
Order 12866 due to its lack of significance, this rule is not subject
to Executive Order 13211, Actions Concerning Regulations That
Significantly Affect Energy Supply, Distribution, or Use (66 FR 28355,
May 22, 2001). This final rule does not contain any information
collections subject to OMB approval under the Paperwork Reduction Act
(PRA), 44 U.S.C. 3501 et seq., or impose any enforceable duty or
contain any unfunded mandate as described under Title II of the
Unfunded Mandates Reform Act of 1995 (UMRA) (Public Law 104-4). 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);
or OMB review or any Agency action under Executive Order 13045,
entitled Protection of Children from Environmental Health Risks and
Safety Risks (62 FR 19885, April 23, 1997). 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 of 1995 (NTTAA),
Public Law 104-113, section 12(d) (15 U.S.C. 272 note). Pursuant to the
requirements of the Regulatory Flexibility Act (RFA) (5 U.S.C. 601 et
seq.), the Agency hereby certifies that this rule will not have
significant negative economic impact on a substantial number of small
entities. In addition, the Agency has determined that this action will
not have a substantial direct effect on States, on the relationship
between the national government and the States, or on the distribution
of power and responsibilities among the various levels of government,
as specified in Executive Order 13132, entitled Federalism (64 FR
43255, August 10, 1999). Executive Order 13132 requires EPA to develop
an accountable process to ensure ``meaningful and timely input by State
and local officials in the development of regulatory policies that have
federalism implications.'' ``Policies that have federalism
implications'' is defined in the Executive order to include regulations
that have ``substantial direct effects on the States, on the
relationship between the national government and the States, or on the
distribution of power and responsibilities among the various levels of
government.'' This final rule directly regulates growers, food
processors, food handlers and food retailers, not States. This action
does not alter the relationships or distribution of power and
responsibilities established by Congress in the preemption provisions
of section 408(n)(4) of FFDCA. For these same reasons, the Agency has
determined that this rule does not have any ``tribal implications'' as
described in Executive Order 13175, entitled Consultation and
Coordination with Indian Tribal Governments (65 FR 67249, November 6,
2000). Executive Order 13175, requires EPA to develop an accountable
process to ensure ``meaningful and timely input by tribal officials in
the development of regulatory policies that have tribal implications.''
``Policies that have tribal implications'' is defined in the Executive
order to include regulations that have ``substantial direct effects on
one or more Indian tribes, on the relationship between the Federal
Government and the Indian tribes, or on the distribution of power and
responsibilities between the Federal Government and Indian tribes.''
This rule will not have substantial direct effects on tribal
governments, on the relationship between the Federal Government and
Indian tribes, or on the distribution of power and responsibilities
between the Federal Government and Indian tribes, as specified in
Executive Order 13175. Thus, Executive Order 13175 does not apply to
this rule.
VII. Congressional Review Act
The Congressional Review Act, 5 U.S.C. 801 et seq., as added by the
Small Business Regulatory Enforcement Fairness Act of 1996, generally
provides that before a rule may take effect, the agency promulgating
the rule must submit a rule report, which includes a copy of the rule,
to each House of the Congress and to the Comptroller General of the
United States. 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 this final rule in the Federal Register. This final
rule 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: April 20, 2005.
Debra Edwards,
Director, Special Review and Reregistration Division, Office of
Pesticide Programs.
0
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. Section 180.207 is amended by adding alphabetically entries for
``peppermint oil,'' and ``spearmint oil'' to the table in paragraph
(a). For the convenience of the reader the entire table to paragraph
(a) is shown below.
Sec. 180.207 Trifluralin; tolerances for residues.
(a) * * *
------------------------------------------------------------------------
Parts per
Commodity million
------------------------------------------------------------------------
Alfalfa, hay............................................... 0.2
Asparagus.................................................. 0.05
Barley, hay................................................ 0.05
Barley, straw.............................................. 0.05
Bean, mung, sprouts........................................ 2.0
Carrot, roots.............................................. 1.0
Corn, field, forage........................................ 0.05
Corn, field, grain......................................... 0.05
Corn, field, stover........................................ 0.05
[[Page 21644]]
Cotton, undelinted seed.................................... 0.05
Cress, upland.............................................. 0.05
Flax, seed................................................. 0.05
Fruit, citrus, group 10.................................... 0.05
Fruit, stone, group 12..................................... 0.05
Grain, crop, except corn, sweet and rice grain............. 0.05
Grape...................................................... 0.05
Hop........................................................ 0.05
Legume, forage............................................. 0.05
Nut, tree, group 14........................................ 0.05
Peanut..................................................... 0.05
Peppermint oil............................................. 2.0
Peppermint, tops........................................... 0.05
Rapeseed, seed............................................. 0.05
Safflower, seed............................................ 0.05
Sorghum, forage............................................ 0.05
Sorghum, grain, stover..................................... 0.05
Spearmint oil.............................................. 2.0
Spearmint, tops............................................ 0.05
Sugarcane, cane............................................ 0.05
Sunflower, seed............................................ 0.05
Vegetable, cucurbit, group 9............................... 0.05
Vegetable, fruiting, group 8............................... 0.05
Vegetables, leafy.......................................... 0.05
Vegetables, root (exc. carrots)............................ 0.05
Vegetables, seed and pod................................... 0.05
Wheat, grain............................................... 0.05
Wheat, straw............................................... 0.05
------------------------------------------------------------------------
* * * * *
[FR Doc. 05-8384 Filed 4-26-05; 8:45 am]
BILLING CODE 6560-50-S