Defensin Proteins (SoD2 and SoD7) Derived From Spinach (Spinacia oleracea L.) in Citrus Plants; Temporary Exemption From the Requirement of a Tolerance, 25943-25946 [2015-10486]
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Federal Register / Vol. 80, No. 87 / Wednesday, May 6, 2015 / Rules and Regulations
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[FR Doc. 2015–10517 Filed 5–5–15; 8:45 am]
BILLING CODE 6750–01–P
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25943
ENVIRONMENTAL PROTECTION
AGENCY
40 CFR Part 174
[EPA–HQ–OPP–2014–0834; FRL–9926–99]
Defensin Proteins (SoD2 and SoD7)
Derived From Spinach (Spinacia
oleracea L.) in Citrus Plants;
Temporary Exemption From the
Requirement of a Tolerance
Environmental Protection
Agency (EPA).
ACTION: Final rule.
AGENCY:
This regulation establishes a
temporary exemption from the
requirement of a tolerance for residues
of SoD2 and SoD7, two defensin
proteins derived from spinach (Spinacia
oleracea L.), in or on citrus when used
as plant-incorporated protectants (PIPs)
in accordance with the terms of
Experimental Use Permit (EUP) No.
88232–EUP–1. Southern Gardens Citrus
submitted a petition to EPA under the
Federal Food, Drug, and Cosmetic Act
(FFDCA), requesting the temporary
tolerance exemption. This regulation
eliminates the need to establish a
maximum permissible level for residues
of SoD2 and SoD7 in or on citrus. The
temporary tolerance exemption expires
on April 18, 2018.
DATES: This regulation is effective May
6, 2015. Objections and requests for
hearings must be received on or before
July 6, 2015, and must be filed in
accordance with the instructions
provided in 40 CFR part 178 (see also
Unit I.C. of the SUPPLEMENTARY
INFORMATION).
SUMMARY:
The docket for this action,
identified by docket identification (ID)
number EPA–HQ–OPP–2014–0834, is
available at https://www.regulations.gov
or at the Office of Pesticide Programs
Regulatory Public Docket (OPP Docket)
in the Environmental Protection Agency
Docket Center (EPA/DC), West William
Jefferson Clinton Bldg., Rm. 3334, 1301
Constitution Ave. NW., Washington, DC
20460–0001. The Public Reading Room
is open from 8:30 a.m. to 4:30 p.m.,
Monday through Friday, excluding legal
holidays. The telephone number for the
Public Reading Room is (202) 566–1744,
and the telephone number for the OPP
Docket is (703) 305–5805. Please review
the visitor instructions and additional
information about the docket available
at https://www.epa.gov/dockets.
FOR FURTHER INFORMATION CONTACT:
Robert McNally, Biopesticides and
Pollution Prevention Division (7511P),
Office of Pesticide Programs,
Environmental Protection Agency, 1200
ADDRESSES:
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Federal Register / Vol. 80, No. 87 / Wednesday, May 6, 2015 / Rules and Regulations
Pennsylvania Ave. NW., Washington,
DC 20460–0001; main telephone
number: (703) 305–7090; email address:
BPPDFRNotices@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. The following
list of North American Industrial
Classification System (NAICS) codes is
not intended to be exhaustive, but rather
provides a guide to help readers
determine whether this document
applies to them. Potentially affected
entities may include:
• Crop production (NAICS code 111).
• Animal production (NAICS code
112).
• Food manufacturing (NAICS code
311).
• Pesticide manufacturing (NAICS
code 32532).
B. How can I get electronic access to
other related information?
You may access a frequently updated
electronic version of 40 CFR part 180
through the Government Publishing
Office’s e-CFR site at https://
www.ecfr.gov/cgi-bin/textidx?&c=ecfr&tpl=/ecfrbrowse/Title40/
40tab_02.tpl.
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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–2014–0834 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 July 6, 2015. 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
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objection or hearing request, identified
by docket ID number EPA–HQ–OPP–
2014–0834, by one of the following
methods:
• Federal eRulemaking Portal: https://
www.regulations.gov. Follow the online
instructions for submitting comments.
Do not submit electronically any
information you consider to be CBI or
other information whose disclosure is
restricted by statute.
• Mail: OPP Docket, Environmental
Protection Agency Docket Center (EPA/
DC), (28221T), 1200 Pennsylvania Ave.
NW., Washington, DC 20460–0001.
• Hand Delivery: To make special
arrangements for hand delivery or
delivery of boxed information, please
follow the instructions at https://
www.epa.gov/dockets/contacts.html.
Additional instructions on
commenting or visiting the docket,
along with more information about
dockets generally, is available at https://
www.epa.gov/dockets.
II. Background and Statutory
Framework
In the Federal Register of January 28,
2015 (80 FR 4525) (FRL–9921–55), EPA
issued a document pursuant to FFDCA
section 408(d)(3), 21 U.S.C. 346a(d)(3),
announcing the filing of a pesticide
tolerance petition (PP 4F8289) by
Southern Gardens Citrus, 1820 Country
Road 833, Clewiston, FL 33440. The
petition requested that 40 CFR part 174
be amended by establishing a temporary
exemption from the requirement of a
tolerance for residues of spinach
defensin (SoD2 and SoD7) proteins in or
on citrus. That document referenced a
summary of the petition prepared by the
petitioner Southern Gardens Citrus,
which is available in the docket, https://
www.regulations.gov. A comment was
received on the notice of filing. EPA’s
response to this comment is discussed
in Unit VII.C.
Section 408(c)(2)(A)(i) of FFDCA
allows EPA to establish an exemption
from the requirement for a tolerance (the
legal limit for a pesticide chemical
residue in or on a food) only if EPA
determines that the exemption is ‘‘safe.’’
Section 408(c)(2)(A)(ii) of FFDCA
defines ‘‘safe ’’ to mean that ‘‘there is a
reasonable certainty that no harm will
result from aggregate exposure to the
pesticide chemical residue, including
all anticipated dietary exposures and all
other exposures for which there is
reliable information.’’ This includes
exposure through drinking water and in
residential settings, but does not include
occupational exposure. Pursuant to
FFDCA section 408(c)(2)(B), in
establishing or maintaining in effect an
exemption from the requirement of a
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tolerance, EPA must take into account
the factors set forth in FFDCA section
408(b)(2)(C), which require EPA to give
special consideration to exposure of
infants and children to the pesticide
chemical residue in establishing a
tolerance and to ‘‘ensure that there is a
reasonable certainty that no harm will
result to infants and children from
aggregate exposure to the pesticide
chemical residue. . . .’’ Additionally,
FFDCA section 408(b)(2)(D) requires
that the Agency consider ‘‘available
information concerning the cumulative
effects of a particular pesticide’s
residues’’ and ‘‘other substances that
have a common mechanism of toxicity.’’
EPA performs a number of analyses to
determine the risks from aggregate
exposure to pesticide residues. First,
EPA determines the toxicity of
pesticides. Second, EPA examines
exposure to the pesticide through food,
drinking water, and through other
exposures that occur as a result of
pesticide use in residential settings.
III. Toxicological Profile
Consistent with FFDCA section
408(b)(2)(D), EPA has reviewed the
available scientific data and other
relevant information in support of this
action and considered its validity,
completeness and reliability, and the
relationship of this information to
human risk. EPA has also considered
available information concerning the
variability of the sensitivities of major
identifiable subgroups of consumers,
including infants and children.
Diverse defensin proteins are
expressed by most eukaryotic species to
combat various bacterial and fungal
organisms. Homologous proteins have
also diverged in evolution to provide
functions related to plant stresses such
as heat and drought.
There is a long history of mammalian
consumption of the entire spinach plant
(both raw and cooked) as food, without
causing any known deleterious human
health effects or any evidence of
toxicity. Spinach plant leaves have long
been part of the human diet and there
have been no findings that indicate
toxicity or allergenicity of spinach
proteins. Spinach is commonly regarded
as a ‘‘super food’’ that serves as an
excellent source of vitamins, minerals,
and antioxidants. Recent U.S.
consumption statistics indicate that, on
average, 2 lbs. of spinach are consumed
per person per year in the United States.
‘‘Spinach Profile,’’ Agricultural
Marketing Resource Center (June 2013)
(https://www.agmrc.org/commodities_
products/vegetables/spinach-profile/).
Similarly, citrus whole fruits and juices
have been an important part of the
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American and international diets for
centuries. ‘‘History of Citrus,’’ All Foods
Natural (2013) (available online at:
https://www.allfoodnatural.com/article/
history-of-citrus.html). Available studies
demonstrate that spinach defensin 2
(SoD2) and spinach defensin 7 (SoD7)
proteins have very low oral toxicity. In
an acute oral toxicity study conducted
with a single dose of 5,000 milligram/
kilogram (mg/kg) of microbial-produced
SoD2 protein, no evidence of toxic or
adverse effects was observed. Due to the
high similarity between SoD2 and SoD7,
the toxicity assessment is applicable to
both proteins.
In an in vitro study, microbialproduced SoD2 and SoD7 proteins were
rapidly and extensively hydrolyzed in
stimulated gastric and intestinal
conditions in the presence of pepsin (at
pH 1.2) and pancreatin, respectively.
Both microbial-produced SoD2 and
SoD7 proteins demonstrated half-lives
of approximately five minutes when
subjected to pepsin digest, and both
proteins were completely proteolyzed to
amino acids and small peptide
fragments in less than one minute in the
presence of 0.15 milligram/liter (mg/ml)
pancreatin. These results indicate that
both the SoD2 and SoD7 proteins are
highly susceptible to degradation in
conditions similar to the human
digestive tract.
A literature search was performed to
identify any published studies that
might implicate these spinach proteins
as allergens. No scientific references
were found to suggest possible
allergenicity associated with these
spinach proteins. Sequence
comparisons were made between the
novel proteins from spinach, SoD2 and
SoD7, against those of known and
putative allergens using FASTA3 to
search the AllergenOnline.org database
using full-length matches, sliding
window of 80 amino acids and finally
8-mer identity searches. In addition, the
sequences were searched against the
National Center for Biotechnology
Information (NCBI) Protein database
without keyword limits to identify
highly related proteins and with the
keyword limit of allergen, to find any
high scoring identity matches to
proteins annotated as allergens, as a
check on the AllergenOnline.org data.
No significant sequence matches were
found between either SoD2 or SoD7 and
any allergens. Thus there are no
potential safety concerns related to
allergenicity that would require further
testing.
IV. Aggregate Exposures
In examining aggregate exposure,
FFDCA section 408 directs EPA to
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consider available information
concerning exposures from the pesticide
residue in food and all other nonoccupational exposures, including
drinking water from ground water or
surface water and exposure through
pesticide use in gardens, lawns, or
buildings (residential and other indoor
uses).
The Agency has considered available
information on the aggregate exposure
levels of consumers (and major
identifiable subgroups of consumers) to
the pesticide chemical residue and to
other related substances. These
considerations include dietary exposure
under the tolerance exemption and all
other tolerances or exemptions in effect
for the plant-incorporated protectant
chemical residue, and exposure from
non-occupational sources. The Agency
anticipates that there may be dietary
exposure to the pesticide from the
consumption of citrus products. In
addition, people have a long history of
consumption of spinach and will
continue to be exposed to defensin
proteins through consumption of
spinach. Since the PIP is integrated into
the plants genome, the Agency has
concluded, based upon previous science
reviews, that residues in drinking water
will be extremely low or non-existent.
Non-occupational exposure via the skin
or inhalation is not likely since the
plant-incorporated protectant is
contained within plant cells, which
essentially eliminates these exposure
routes or reduces these exposure routes
to negligible. In any event, there are no
non-dietary non-occupational uses of
SoD2 and SoD7 as it is only used in
agricultural settings.
V. Cumulative Effects From Substances
With a Common Mechanism of Toxicity
Section 408(b)(2)(D)(v) of FFDCA
requires that, when considering whether
to establish, modify, or revoke a
tolerance, the Agency consider
‘‘available information’’ concerning the
cumulative effects of a particular
pesticide’s residues and ‘‘other
substances that have a common
mechanism of toxicity.’’
Since SoD2 and SoD7 proteins do not
act through a toxic mode of action nor
do the SoD2 and SoD7 proteins appear
to produce a toxic metabolite produced
by other substances, the proteins do not
have a common mechanism of toxicity
with other substances; therefore, the
requirements of section 408(b)(2)(D)(v)
do not apply.
VI. Determination of Safety for U.S.
Population, Infants and Children
FFDCA section 408(b)(2)(C) provides
that, in considering the establishment of
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25945
a tolerance or tolerance exemption for a
pesticide chemical residue, EPA shall
assess the available information about
consumption patterns among infants
and children, special susceptibility of
infants and children to pesticide
chemical residues, and the cumulative
effects on infants and children of the
residues and other substances with a
common mechanism of toxicity. In
addition, FFDCA section 408(b)(2)(C)
provides that EPA shall apply an
additional tenfold (10X) margin of
exposure (safety) for infants and
children in the case of threshold effects
to account for prenatal and postnatal
toxicity and the completeness of the
database on toxicity and exposure
unless EPA determines that a different
margin of exposure (safety) will be safe
for infants and children. This additional
margin of exposure (safety) is commonly
referred to as the Food Quality
Protection Act Safety Factor (FQPA SF).
In applying this provision, EPA either
retains the default value of 10X or uses
a different additional safety factor when
reliable data available to EPA support
the choice of a different factor.
Based on the information discussed in
Unit III., EPA concludes that there are
no threshold effects of concern to
infants, children, or adults from
exposure to the spinach defensin
proteins SoD2 and SoD7. As a result,
EPA concludes that no additional
margin of exposure (safety) is necessary
to protect infants and children and that
not adding any additional margin of
exposure (safety) will be safe for infants
and children.
Therefore, based on the discussion in
Units III and IV, EPA concludes that
there is a reasonable certainty that no
harm will result to the U.S. population,
including infants and children, from
aggregate exposure to the residues of
spinach defensin proteins SoD2 and
SoD7 in citrus, when it is used as a
plant-incorporated protectant. Such
exposure includes all anticipated
dietary exposures and all other
exposures for which there is reliable
information. The Agency has arrived at
this conclusion based on a lack of
toxicity and allergenicity of the SoD2
and SoD7 proteins.
VII. Other Considerations
A. Endocrine Disruptors
The pesticidal active ingredient is a
protein, derived from a source that is
not known to exert an influence on the
endocrine system. Therefore, the
Agency is not requiring information on
the endocrine effects of the plantincorporated protectant at this time.
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B. Analytical Enforcement Methodology
A standard operating procedure for an
enzyme-linked immunosorbent assay for
the detection and quantification of
spinach defensin proteins SoD2 and
SoD7 in citrus plant tissue has been
judged useful for its intended purpose.
C. Response to Comments
EPA received one comment relevant
to this petition. The comment supports
this tolerance exemption and therefore
warrants no response.
VIII. Conclusion
The Agency concludes that there is a
reasonable certainty that no harm will
result to the U.S. population, including
infants and children, from aggregate
exposure residues of spinach defensin
SoD2 and SoD7 proteins in or on citrus.
This includes all anticipated dietary
exposures and all other exposures for
which there is reliable information. The
Agency has arrived at this conclusion
because, as discussed previously no
toxicity to mammals has been observed,
nor is there any indication of
allergenicity potential for the plantincorporated protectant.
Therefore, an exemption is
established for residues of spinach
defensin SoD2 and SoD7 proteins in or
on citrus when the protein is used as a
PIP in citrus plants.
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IX. Statutory and Executive Order
Reviews
This action establishes a temporary
exemption from the requirement of a
tolerance 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).
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
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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 exemption 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).
X. Congressional Review Act
List of Subjects in 40 CFR Part 174
Environmental protection,
Administrative practice and procedure,
Agricultural commodities, Pesticides
and pests, Reporting and recordkeeping
requirements.
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Therefore, 40 CFR chapter I is
amended as follows:
PART 174—[AMENDED]
1. The authority citation for part 174
continues to read as follows:
■
Authority: 21 U.S.C. 321(q), 346a and 371.
2. Add § 174.535 to subpart W to read
as follows:
■
§ 174.535 Spinach Defensin proteins;
temporary exemption from the requirement
of a tolerance.
(a) Residues of the defensin protein
SoD2 derived from spinach (Spinacia
oleracea L.) in or on citrus food
commodities are temporarily exempt
from the requirement of a tolerance
when used as a plant-incorporated
protectant in citrus plants in accordance
with the terms of Experimental Use
Permit No. 88232–EUP–1. This
temporary exemption from the
requirement of a tolerance expires on
April 18, 2018.
(b) Residues of the defensin protein
SoD7 derived from spinach (Spinacia
oleracea L.) in or on citrus food
commodities are temporarily exempt
from the requirement of a tolerance
when used as a plant-incorporated
protectant in citrus plants in accordance
with the terms of Experimental Use
Permit No. 88232–EUP–1. This
temporary exemption from the
requirement of a tolerance expires on
April 18, 2018.
[FR Doc. 2015–10486 Filed 5–5–15; 8:45 am]
BILLING CODE 6560–50–P
ENVIRONMENTAL PROTECTION
AGENCY
40 CFR Part 174
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).
PO 00000
Dated: April 28, 2015.
Robert McNally,
Director, Biopesticides and Pollution
Prevention Division, Office of Pesticide
Programs.
[EPA–HQ–OPP–2014–0454; FRL–9926–23]
Bacillus thuringiensis Cry1A.105
Protein in Soybean; Exemption From
the Requirement of a Tolerance
Environmental Protection
Agency (EPA).
ACTION: Final rule.
AGENCY:
This regulation establishes an
exemption from the requirement of a
tolerance for residues of the Bacillus
thuringiensis (B.t.) Cry1A.105 protein in
or on soybean when the protein is used
as a plant-incorporated protectant (PIP)
in soybean. Monsanto Company
submitted a petition to EPA under the
SUMMARY:
E:\FR\FM\06MYR1.SGM
06MYR1
Agencies
[Federal Register Volume 80, Number 87 (Wednesday, May 6, 2015)]
[Rules and Regulations]
[Pages 25943-25946]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2015-10486]
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ENVIRONMENTAL PROTECTION AGENCY
40 CFR Part 174
[EPA-HQ-OPP-2014-0834; FRL-9926-99]
Defensin Proteins (SoD2 and SoD7) Derived From Spinach (Spinacia
oleracea L.) in Citrus Plants; Temporary Exemption From the Requirement
of a Tolerance
AGENCY: Environmental Protection Agency (EPA).
ACTION: Final rule.
-----------------------------------------------------------------------
SUMMARY: This regulation establishes a temporary exemption from the
requirement of a tolerance for residues of SoD2 and SoD7, two defensin
proteins derived from spinach (Spinacia oleracea L.), in or on citrus
when used as plant-incorporated protectants (PIPs) in accordance with
the terms of Experimental Use Permit (EUP) No. 88232-EUP-1. Southern
Gardens Citrus submitted a petition to EPA under the Federal Food,
Drug, and Cosmetic Act (FFDCA), requesting the temporary tolerance
exemption. This regulation eliminates the need to establish a maximum
permissible level for residues of SoD2 and SoD7 in or on citrus. The
temporary tolerance exemption expires on April 18, 2018.
DATES: This regulation is effective May 6, 2015. Objections and
requests for hearings must be received on or before July 6, 2015, 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-2014-0834, is available at https://www.regulations.gov or at the Office of Pesticide Programs Regulatory
Public Docket (OPP Docket) in the Environmental Protection Agency
Docket Center (EPA/DC), West William Jefferson Clinton Bldg., Rm. 3334,
1301 Constitution Ave. NW., Washington, DC 20460-0001. The Public
Reading Room is open from 8:30 a.m. to 4:30 p.m., Monday through
Friday, excluding legal holidays. The telephone number for the Public
Reading Room is (202) 566-1744, and the telephone number for the OPP
Docket is (703) 305-5805. Please review the visitor instructions and
additional information about the docket available at https://www.epa.gov/dockets.
FOR FURTHER INFORMATION CONTACT: Robert McNally, Biopesticides and
Pollution Prevention Division (7511P), Office of Pesticide Programs,
Environmental Protection Agency, 1200
[[Page 25944]]
Pennsylvania Ave. NW., Washington, DC 20460-0001; main telephone
number: (703) 305-7090; email address: BPPDFRNotices@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.
The following list of North American Industrial Classification System
(NAICS) codes is not intended to be exhaustive, but rather provides a
guide to help readers determine whether this document applies to them.
Potentially affected entities may include:
Crop production (NAICS code 111).
Animal production (NAICS code 112).
Food manufacturing (NAICS code 311).
Pesticide manufacturing (NAICS code 32532).
B. How can I get electronic access to other related information?
You may access a frequently updated electronic version of 40 CFR
part 180 through the Government Publishing Office's e-CFR site at
https://www.ecfr.gov/cgi-bin/text-idx?&c=ecfr&tpl=/ecfrbrowse/Title40/40tab_02.tpl.
C. How can I file an objection or hearing request?
Under FFDCA section 408(g), 21 U.S.C. 346a, 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-2014-0834 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
July 6, 2015. 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-2014-0834, by one of
the following methods:
Federal eRulemaking Portal: https://www.regulations.gov.
Follow the online instructions for submitting comments. Do not submit
electronically any information you consider to be CBI or other
information whose disclosure is restricted by statute.
Mail: OPP Docket, Environmental Protection Agency Docket
Center (EPA/DC), (28221T), 1200 Pennsylvania Ave. NW., Washington, DC
20460-0001.
Hand Delivery: To make special arrangements for hand
delivery or delivery of boxed information, please follow the
instructions at https://www.epa.gov/dockets/contacts.html.
Additional instructions on commenting or visiting the docket, along
with more information about dockets generally, is available at https://www.epa.gov/dockets.
II. Background and Statutory Framework
In the Federal Register of January 28, 2015 (80 FR 4525) (FRL-9921-
55), EPA issued a document pursuant to FFDCA section 408(d)(3), 21
U.S.C. 346a(d)(3), announcing the filing of a pesticide tolerance
petition (PP 4F8289) by Southern Gardens Citrus, 1820 Country Road 833,
Clewiston, FL 33440. The petition requested that 40 CFR part 174 be
amended by establishing a temporary exemption from the requirement of a
tolerance for residues of spinach defensin (SoD2 and SoD7) proteins in
or on citrus. That document referenced a summary of the petition
prepared by the petitioner Southern Gardens Citrus, which is available
in the docket, https://www.regulations.gov. A comment was received on
the notice of filing. EPA's response to this comment is discussed in
Unit VII.C.
Section 408(c)(2)(A)(i) of FFDCA allows EPA to establish an
exemption from the requirement for a tolerance (the legal limit for a
pesticide chemical residue in or on a food) only if EPA determines that
the exemption is ``safe.'' Section 408(c)(2)(A)(ii) of FFDCA defines
``safe '' to mean that ``there is a reasonable certainty that no harm
will result from aggregate exposure to the pesticide chemical residue,
including all anticipated dietary exposures and all other exposures for
which there is reliable information.'' This includes exposure through
drinking water and in residential settings, but does not include
occupational exposure. Pursuant to FFDCA section 408(c)(2)(B), in
establishing or maintaining in effect an exemption from the requirement
of a tolerance, EPA must take into account the factors set forth in
FFDCA section 408(b)(2)(C), which require EPA to give special
consideration to exposure of infants and children to the pesticide
chemical residue in establishing a tolerance and to ``ensure that there
is a reasonable certainty that no harm will result to infants and
children from aggregate exposure to the pesticide chemical residue. . .
.'' Additionally, FFDCA section 408(b)(2)(D) requires that the Agency
consider ``available information concerning the cumulative effects of a
particular pesticide's residues'' and ``other substances that have a
common mechanism of toxicity.''
EPA performs a number of analyses to determine the risks from
aggregate exposure to pesticide residues. First, EPA determines the
toxicity of pesticides. Second, EPA examines exposure to the pesticide
through food, drinking water, and through other exposures that occur as
a result of pesticide use in residential settings.
III. Toxicological Profile
Consistent with FFDCA section 408(b)(2)(D), EPA has reviewed the
available scientific data and other relevant information in support of
this action and considered its validity, completeness and reliability,
and the relationship of this information to human risk. EPA has also
considered available information concerning the variability of the
sensitivities of major identifiable subgroups of consumers, including
infants and children.
Diverse defensin proteins are expressed by most eukaryotic species
to combat various bacterial and fungal organisms. Homologous proteins
have also diverged in evolution to provide functions related to plant
stresses such as heat and drought.
There is a long history of mammalian consumption of the entire
spinach plant (both raw and cooked) as food, without causing any known
deleterious human health effects or any evidence of toxicity. Spinach
plant leaves have long been part of the human diet and there have been
no findings that indicate toxicity or allergenicity of spinach
proteins. Spinach is commonly regarded as a ``super food'' that serves
as an excellent source of vitamins, minerals, and antioxidants. Recent
U.S. consumption statistics indicate that, on average, 2 lbs. of
spinach are consumed per person per year in the United States.
``Spinach Profile,'' Agricultural Marketing Resource Center (June 2013)
(https://www.agmrc.org/commodities_products/vegetables/spinach-profile/
). Similarly, citrus whole fruits and juices have been an important
part of the
[[Page 25945]]
American and international diets for centuries. ``History of Citrus,''
All Foods Natural (2013) (available online at: https://www.allfoodnatural.com/article/history-of-citrus.html). Available
studies demonstrate that spinach defensin 2 (SoD2) and spinach defensin
7 (SoD7) proteins have very low oral toxicity. In an acute oral
toxicity study conducted with a single dose of 5,000 milligram/kilogram
(mg/kg) of microbial-produced SoD2 protein, no evidence of toxic or
adverse effects was observed. Due to the high similarity between SoD2
and SoD7, the toxicity assessment is applicable to both proteins.
In an in vitro study, microbial-produced SoD2 and SoD7 proteins
were rapidly and extensively hydrolyzed in stimulated gastric and
intestinal conditions in the presence of pepsin (at pH 1.2) and
pancreatin, respectively. Both microbial-produced SoD2 and SoD7
proteins demonstrated half-lives of approximately five minutes when
subjected to pepsin digest, and both proteins were completely
proteolyzed to amino acids and small peptide fragments in less than one
minute in the presence of 0.15 milligram/liter (mg/ml) pancreatin.
These results indicate that both the SoD2 and SoD7 proteins are highly
susceptible to degradation in conditions similar to the human digestive
tract.
A literature search was performed to identify any published studies
that might implicate these spinach proteins as allergens. No scientific
references were found to suggest possible allergenicity associated with
these spinach proteins. Sequence comparisons were made between the
novel proteins from spinach, SoD2 and SoD7, against those of known and
putative allergens using FASTA3 to search the AllergenOnline.org
database using full-length matches, sliding window of 80 amino acids
and finally 8-mer identity searches. In addition, the sequences were
searched against the National Center for Biotechnology Information
(NCBI) Protein database without keyword limits to identify highly
related proteins and with the keyword limit of allergen, to find any
high scoring identity matches to proteins annotated as allergens, as a
check on the AllergenOnline.org data. No significant sequence matches
were found between either SoD2 or SoD7 and any allergens. Thus there
are no potential safety concerns related to allergenicity that would
require further testing.
IV. Aggregate Exposures
In examining aggregate exposure, FFDCA section 408 directs EPA to
consider available information concerning exposures from the pesticide
residue in food and all other non-occupational exposures, including
drinking water from ground water or surface water and exposure through
pesticide use in gardens, lawns, or buildings (residential and other
indoor uses).
The Agency has considered available information on the aggregate
exposure levels of consumers (and major identifiable subgroups of
consumers) to the pesticide chemical residue and to other related
substances. These considerations include dietary exposure under the
tolerance exemption and all other tolerances or exemptions in effect
for the plant-incorporated protectant chemical residue, and exposure
from non-occupational sources. The Agency anticipates that there may be
dietary exposure to the pesticide from the consumption of citrus
products. In addition, people have a long history of consumption of
spinach and will continue to be exposed to defensin proteins through
consumption of spinach. Since the PIP is integrated into the plants
genome, the Agency has concluded, based upon previous science reviews,
that residues in drinking water will be extremely low or non-existent.
Non-occupational exposure via the skin or inhalation is not likely
since the plant-incorporated protectant is contained within plant
cells, which essentially eliminates these exposure routes or reduces
these exposure routes to negligible. In any event, there are no non-
dietary non-occupational uses of SoD2 and SoD7 as it is only used in
agricultural settings.
V. Cumulative Effects From Substances With a Common Mechanism of
Toxicity
Section 408(b)(2)(D)(v) of FFDCA requires that, when considering
whether to establish, modify, or revoke a tolerance, the Agency
consider ``available information'' concerning the cumulative effects of
a particular pesticide's residues and ``other substances that have a
common mechanism of toxicity.''
Since SoD2 and SoD7 proteins do not act through a toxic mode of
action nor do the SoD2 and SoD7 proteins appear to produce a toxic
metabolite produced by other substances, the proteins do not have a
common mechanism of toxicity with other substances; therefore, the
requirements of section 408(b)(2)(D)(v) do not apply.
VI. Determination of Safety for U.S. Population, Infants and Children
FFDCA section 408(b)(2)(C) provides that, in considering the
establishment of a tolerance or tolerance exemption for a pesticide
chemical residue, EPA shall assess the available information about
consumption patterns among infants and children, special susceptibility
of infants and children to pesticide chemical residues, and the
cumulative effects on infants and children of the residues and other
substances with a common mechanism of toxicity. In addition, FFDCA
section 408(b)(2)(C) provides that EPA shall apply an additional
tenfold (10X) margin of exposure (safety) for infants and children in
the case of threshold effects to account for prenatal and postnatal
toxicity and the completeness of the database on toxicity and exposure
unless EPA determines that a different margin of exposure (safety) will
be safe for infants and children. This additional margin of exposure
(safety) is commonly referred to as the Food Quality Protection Act
Safety Factor (FQPA SF). In applying this provision, EPA either retains
the default value of 10X or uses a different additional safety factor
when reliable data available to EPA support the choice of a different
factor.
Based on the information discussed in Unit III., EPA concludes that
there are no threshold effects of concern to infants, children, or
adults from exposure to the spinach defensin proteins SoD2 and SoD7. As
a result, EPA concludes that no additional margin of exposure (safety)
is necessary to protect infants and children and that not adding any
additional margin of exposure (safety) will be safe for infants and
children.
Therefore, based on the discussion in Units III and IV, EPA
concludes that there is a reasonable certainty that no harm will result
to the U.S. population, including infants and children, from aggregate
exposure to the residues of spinach defensin proteins SoD2 and SoD7 in
citrus, when it is used as a plant-incorporated protectant. Such
exposure includes all anticipated dietary exposures and all other
exposures for which there is reliable information. The Agency has
arrived at this conclusion based on a lack of toxicity and
allergenicity of the SoD2 and SoD7 proteins.
VII. Other Considerations
A. Endocrine Disruptors
The pesticidal active ingredient is a protein, derived from a
source that is not known to exert an influence on the endocrine system.
Therefore, the Agency is not requiring information on the endocrine
effects of the plant-incorporated protectant at this time.
[[Page 25946]]
B. Analytical Enforcement Methodology
A standard operating procedure for an enzyme-linked immunosorbent
assay for the detection and quantification of spinach defensin proteins
SoD2 and SoD7 in citrus plant tissue has been judged useful for its
intended purpose.
C. Response to Comments
EPA received one comment relevant to this petition. The comment
supports this tolerance exemption and therefore warrants no response.
VIII. Conclusion
The Agency concludes that there is a reasonable certainty that no
harm will result to the U.S. population, including infants and
children, from aggregate exposure residues of spinach defensin SoD2 and
SoD7 proteins in or on citrus. This includes all anticipated dietary
exposures and all other exposures for which there is reliable
information. The Agency has arrived at this conclusion because, as
discussed previously no toxicity to mammals has been observed, nor is
there any indication of allergenicity potential for the plant-
incorporated protectant.
Therefore, an exemption is established for residues of spinach
defensin SoD2 and SoD7 proteins in or on citrus when the protein is
used as a PIP in citrus plants.
IX. Statutory and Executive Order Reviews
This action establishes a temporary exemption from the requirement
of a tolerance 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). 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 exemption 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).
X. 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 174
Environmental protection, Administrative practice and procedure,
Agricultural commodities, Pesticides and pests, Reporting and
recordkeeping requirements.
Dated: April 28, 2015.
Robert McNally,
Director, Biopesticides and Pollution Prevention Division, Office of
Pesticide Programs.
Therefore, 40 CFR chapter I is amended as follows:
PART 174--[AMENDED]
0
1. The authority citation for part 174 continues to read as follows:
Authority: 21 U.S.C. 321(q), 346a and 371.
0
2. Add Sec. 174.535 to subpart W to read as follows:
Sec. 174.535 Spinach Defensin proteins; temporary exemption from the
requirement of a tolerance.
(a) Residues of the defensin protein SoD2 derived from spinach
(Spinacia oleracea L.) in or on citrus food commodities are temporarily
exempt from the requirement of a tolerance when used as a plant-
incorporated protectant in citrus plants in accordance with the terms
of Experimental Use Permit No. 88232-EUP-1. This temporary exemption
from the requirement of a tolerance expires on April 18, 2018.
(b) Residues of the defensin protein SoD7 derived from spinach
(Spinacia oleracea L.) in or on citrus food commodities are temporarily
exempt from the requirement of a tolerance when used as a plant-
incorporated protectant in citrus plants in accordance with the terms
of Experimental Use Permit No. 88232-EUP-1. This temporary exemption
from the requirement of a tolerance expires on April 18, 2018.
[FR Doc. 2015-10486 Filed 5-5-15; 8:45 am]
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