[Federal Register Volume 75, Number 16 (Tuesday, January 26, 2010)]
[Rules and Regulations]
[Pages 4228-4253]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2010-1375]
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Part IV
Department of Agriculture
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Animal and Plant Health Inspection Service
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7 CFR Parts 301, 305, 318, et al.
Phytosanitary Treatments; Location of and Process for Updating
Treatment Schedules; Final Rule
Federal Register / Vol. 75, No. 16 / Tuesday, January 26, 2010 /
Rules and Regulations
[[Page 4228]]
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DEPARTMENT OF AGRICULTURE
Animal and Plant Health Inspection Service
7 CFR Parts 301, 305, 318, 319, 330, and 352
[Docket No. APHIS-2008-0022]
RIN 0579-AC94
Phytosanitary Treatments; Location of and Process for Updating
Treatment Schedules
AGENCY: Animal and Plant Health Inspection Service, USDA.
ACTION: Final rule.
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SUMMARY: We are amending the phytosanitary treatment regulations in 7
CFR part 305 by removing the lists of approved treatments and treatment
schedules from the regulations, while retaining the general
requirements for performing treatments and certifying or approving
treatment facilities. We are removing treatment schedules from other
places where they are currently found in 7 CFR chapter III as well.
Approved treatment schedules will instead be found in the Plant
Protection and Quarantine Treatment Manual, which is available on the
Internet. We are also establishing a new process to provide the public
with notice and the opportunity to comment on changes to treatment
schedules. Finally, we are harmonizing and combining the requirements
for performing irradiation treatment for imported articles, articles
moved interstate from Hawaii and U.S. territories, and articles moved
interstate from an area quarantined for fruit flies. These changes will
simplify and expedite our processes for adding, changing, and removing
treatment schedules while continuing to provide for public
participation in the process. These changes will also simplify our
presentation of treatments to the public by consolidating all
treatments into one document and eliminating redundant text from the
regulations.
EFFECTIVE DATE: February 25, 2010.
FOR FURTHER INFORMATION CONTACT: Dr. Inder P. S. Gadh, Senior Risk
Manager-Treatments, Regulations, Permits, and Manuals, PPQ, APHIS, 4700
River Road Unit 133, Riverdale, MD 20737-1236; (301) 734-0627.
SUPPLEMENTARY INFORMATION:
Background
The regulations in 7 CFR chapter III are intended, among other
things, to prevent the introduction or dissemination of plant pests and
noxious weeds into or within the United States. Under the regulations,
certain plants, fruits, vegetables, and other articles must be treated
before they may be moved into the United States or interstate. The
phytosanitary treatments regulations contained in part 305 of 7 CFR
chapter III (referred to below as the regulations) set out standards
and schedules for treatments required in parts 301, 318, and 319 of 7
CFR chapter III for fruits, vegetables, and other articles.
On May 12, 2009, we published in the Federal Register (74 FR 22318-
22345, Docket No. APHIS-2008-0022) a proposal\1\ to amend the
regulations by removing the lists of approved treatments and treatment
schedules from the regulations, while retaining the general
requirements for performing treatments and certifying or approving
treatment facilities. We proposed to remove treatment schedules from
other places where they are currently found in 7 CFR chapter III as
well, instead listing approved treatment schedules in the Plant
Protection and Quarantine (PPQ) Treatment Manual, which is available on
the Internet.\2\ We also proposed to establish a new process to provide
the public with notice and the opportunity to comment on changes to
treatment schedules. Finally, we proposed to harmonize and combine the
requirements for performing irradiation treatment for imported
articles, articles moved interstate from Hawaii and U.S. territories,
and articles moved interstate from an area quarantined for fruit flies.
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\1\ To view the proposed rule and the comments we received, go
to (http://www.regulations.gov/fdmspublic/component/main?main=DocketDetail&d=APHIS-2008-0022).
\2\ At (http://www.aphis.usda.gov/import_export/plants/manuals/ports/treatment.shtml).
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We solicited comments concerning our proposal for 60 days ending
July 13, 2009. We received 14 comments by that date. They were from
nursery owners, academics, treatment facility operators, and
representatives of State and foreign governments. They are discussed
below by topic.
General Comments About the Treatment Requirements
As part of proposing to remove treatment schedules from 7 CFR
chapter III, we proposed to move the general requirements for each type
of treatment (chemical treatment, cold treatment, etc.) in 7 CFR part
305 to new locations within that part. We also proposed to make some
minor changes to the existing treatment requirements.
One commenter suggested that we identify the common requirements
for all treatments in the remaining provisions of 7 CFR part 305 and
present them in an introductory section, setting out specific
requirements for the individual types of treatments in later sections.
The commenter also suggested that there is a common set of mitigations
for fruit flies (packaging, product movement, and location of treatment
facilities) that could be contained in a separate section and
referenced in the appropriate treatment requirements. The commenter
stated that such changes would provide more clarity in the specific
treatment requirements while creating more certainty that all
regulations governing treatment in part 305 are included without
unnecessary repetition.
As we proposed to move the treatment requirements but not to make
any significant changes to them, making large-scale revisions to those
requirements would be outside the scope of this final rule. However, we
appreciate the commenter's suggestion and will consider whether to make
such changes in a future rulemaking.
One commenter stated that there are inconsistencies in how the
terms ``approve,'' ``authorize,'' and ``certify'' are used in the
existing treatment requirements. The commenter pointed out that
proposed Sec. 305.5(a), which contains requirements for chemical
treatment facilities, is headed ``Certified facility,'' while proposed
Sec. 305.6(a), which contains requirements for cold treatment
facilities, is headed ``Approval of treatment facilities.'' (Paragraph
(a) of proposed Sec. 305.8(a), which contains requirements for heat
treatment facilities, is also headed ``Certified facility.'') The
commenter stated that authorization of a quarantine treatment facility
may be a complex process that could include licenses from local, State,
or Federal regulatory agencies other than the Animal and Plant Health
Inspection Service (APHIS), or a foreign national plant protection
organization (NPPO), in the case of foreign facilities. The commenter
stated that ``certification'' would be a more appropriate term for the
process undertaken by APHIS or a foreign NPPO to ensure that a facility
can consistently perform efficacious phytosanitary treatments,
including post-treatment safeguarding and documentation.
Another commenter stated that proposed Sec. 305.9(b), which
referred to approval of an irradiation facility by APHIS, should
instead refer to certification of the irradiation facility by APHIS.
We agree with the first commenter's general point that a
distinction should be drawn between certification of a facility as
capable of performing treatment and approval of that facility to
[[Page 4229]]
perform treatments. In proposed Sec. 305.9, which contained our
proposed revision of the irradiation treatment requirements, we
referred to certification of a facility as part of the process for
approval of a facility; the other part of that process was completing
the necessary compliance agreements or workplans. Our use of the term
``certification'' in proposed Sec. Sec. 305.5 and 305.8 was consistent
with the use in proposed Sec. 305.9. To be consistent, this final rule
refers to certification, rather than approval, of cold treatment
facilities in Sec. 305.6(a). For reasons mentioned earlier, we are not
making the change suggested by the second commenter.
Definitions
We proposed to add or change the definitions of some terms in Sec.
305.1.
The definition of irradiation has read: ``The use of irradiated
energy to kill or devitalize organisms.'' We proposed to replace the
reference to ``irradiated energy'' with a reference to ``ionized
energy.'' We also proposed to replace the reference to ``devitalize''
in the definition of irradiation with a reference to ``neutralize.''
Two commenters suggested that we refer instead to ``ionizing
energy,'' as it is not the energy itself that is ionized; rather, the
energy has the effect of ionizing atoms that are hit by the
irradiation.
We agree with these commenters.
One commenter suggested that we add the word ``pest'' before the
word ``organisms'' in the definition of irradiation.
The commenter did not provide any specific reason for making this
change. We believe the suggested change is unnecessary, as any organism
for which treatment is required will be a plant pest.
The International Plant Protection Convention's (IPPC) Glossary of
Phytosanitary Terms\3\ defines irradiation as ``treatment with any type
of ionizing radiation.'' As this definition is substantially similar to
the proposed definition, and adopting the IPPC definition would make
the regulations consistent with international standards, we are
adopting the IPPC definition of irradiation in this final rule.
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\3\ The Glossary of Phytosanitary Terms is International
Standard for Phytosanitary Measures (ISPM) Number 5. To view this
and other ISPMs on the Internet, go to (http://www.ippc.int/) and
click on the ``Adopted Standards'' link under the ``Core
activities'' heading.
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We proposed to add a definition of neutralize to reflect the fact
that an effective irradiation treatment does not necessarily kill a
plant pest. The proposed definition of neutralize read: ``In the case
of treatments other than irradiation, to kill a plant pest; in the case
of irradiation, to prevent the establishment of the pest by killing it,
sterilizing it, or preventing its development from an immature stage
into an adult capable of emerging from its host, reproducing, or
becoming established.''
Two commenters recommended that the definition of neutralize make
no distinction between irradiation and other treatments. One commenter
noted that stating that treatments other than irradiation must result
in the death of a plant pest does not provide options for other
treatments that may be demonstrated to achieve a quarantine objective
without causing mortality. For example, the commenter stated, the use
of juvenile hormones as a treatment would prevent the development of
larva into adults, while not killing the insect directly. In this case,
the quarantine objective would be met, as the pest would not be able to
reproduce and establish. While such treatments are not currently
approved under the regulations or within the PPQ Treatment Manual, the
commenter stated that, should such treatments be approved, it would be
beneficial to allow for their subsequent inclusion within the PPQ
Treatment Manual without having to amend the definition of neutralize.
We agree with these commenters and have removed the distinction
between methods of treatment in the definition of neutralize in this
final rule.
One commenter recommended that we remove the phrase ``reproducing
or becoming established'' from the proposed definition of neutralize
and instead refer to preventing a pest's development from an immature
stage into an adult capable of emerging from its host or pupal case. As
both non-emergence of adults and sterility of any life stage would
effectively prevent a pest from reproducing and thereby becoming
established, the commenter stated that highlighting that both of these
are potentially acceptable outcomes would allow for the different
biology of the range of pests for which a quarantine treatment might be
applied.
We agree with the commenter's general point. However, with regard
to the specific suggested language, ``pupal case'' would be
inappropriately limiting, as a treatment that prevented development of
pests in the larval stage would also be considered to be effective.
Referring generally to preventing the development of a pest from an
immature stage will encompass all of the potential successful outcomes.
We have changed the proposed definition of neutralize accordingly.
With these changes, the definition of neutralize in this final rule
reads: ``To prevent the establishment of a plant pest by killing it,
sterilizing it, preventing its development from an immature stage, or
preventing its emergence from its host.''
One commenter suggested that we add a definition of the term
monitor, a term used in the general treatment requirements. The
commenter stated that readers could be confused regarding whether
monitor implies constant oversight of the treatment process or
validation of the process at critical points in time.
The tenth edition of Merriam-Webster's Collegiate Dictionary
defines ``monitor'' as ``to keep watch of, track, or check.'' Other
dictionaries provide similar definitions. This definition indicates
that monitoring occurs while the treatment is occurring, but does not
necessarily indicate constant oversight, which is consistent with the
monitoring that officials authorized by APHIS perform for treatments.
The IPPC Glossary of Phytosanitary Terms is consistent with the general
definition, defining monitoring as ``an official ongoing process to
verify phytosanitary situations.'' We do not see a need to add a
definition of monitor to the regulations, since our use of monitor is
consistent with common understanding of the term and with international
standards.
Notice-Based Process for Amending Treatments
Proposed Sec. 305.3 set out a notice-based process for amending
approved treatments. We received several comments supporting the use of
such a process. One commenter noted that the addition, revision, and
deletion of treatment schedules will directly affect the interests of
trading partners and asked that APHIS provide notification of such
changes to the World Trade Organization (WTO), with a sufficient period
for comment, so that trading partners will be informed of these changes
in a timely manner.
We plan to provide WTO notifications for notices published under
this process, as we do for other trade-related notices. The notice will
provide for a public comment period during which trading partners, as
well as any other interested parties, may submit comments.
We are making two minor changes to the proposed provisions for the
notice-based process. We are changing paragraph (b)(1)(iii) to refer to
``articles'' rather than ``commodities,'' because
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``articles'' is the more commonly used general term.
In addition, proposed paragraph (b)(2) stated that treatments added
or revised through the process we proposed to use for immediate changes
to treatment schedules would be listed in a separate section of the PPQ
Treatment Manual as having been added or revised through the immediate
process described in proposed paragraph (b). However, in the current
PPQ Treatment Manual, all of the treatments are listed by type
(chemical treatment, cold treatment, etc.), which makes it easy for
facility operators and others to see all the treatments that could
potentially be employed at a specific treatment facility. Listing
treatments approved through the immediate process in a separate section
would make the PPQ Treatment Manual less user-friendly. Therefore, we
have changed this provision in this final rule to indicate that
treatment schedules that have been added to the PPQ Treatment Manual or
revised under this process will be identified in the PPQ Treatment
Manual as having been added or revised through the immediate process.
The identification will make it clear that such treatments may be
subject to change pending the comments we receive on the added or
revised treatments.
Monitoring and Certification of Treatments
Section 305.3 has contained requirements for monitoring and
certification of treatments. We proposed to move these requirements to
Sec. 305.4 and amend them.
Paragraph (b) of Sec. 305.3 has required any treatment performed
outside the United States to be monitored and certified by an inspector
or an official from the NPPO of the exporting country. In proposed
Sec. 305.4(b), we proposed to require instead that any treatment
performed outside the United States must be monitored and certified by
an inspector or an official authorized by APHIS. We proposed this
change to make this requirement consistent with the other requirements
in part 305, which refer to officials authorized by APHIS rather than
NPPO officials specifically.
Three commenters recommended that we not change the language
currently in the regulations. Two commenters stated that the current
regulations allow for APHIS to require preclearance, in which an APHIS
inspector is present during the treatment and certifies that the
treated commodity is free of quarantine pests, or certification by the
NPPO; these commenters objected to what they perceived as the removal
of the latter option.
One of these commenters further noted that international agreements
recognize the NPPO as the official service that certifies consignments
to have been disinfected or disinfested when being moved in
international trade and provides the necessary endorsements on
phytosanitary certificates. This commenter also stated that, unless a
risk assessment demonstrates that preclearance is necessary, requiring
preclearance imposes significant additional costs to exporters without
increasing the quarantine security of consignments. This commenter
recommended that we change the references to ``an official authorized
by APHIS'' in other sections of the regulations to refer to officials
from the NPPO of the exporting country, to be consistent with the
original text of Sec. 305.3.
The provisions we proposed allow everything that is allowed under
the current regulations; we did not propose to remove any options.
Officials authorized by APHIS would include any officials of a foreign
NPPO who currently certify treatments for articles exported to the
United States. They would also include third parties that conduct
treatments. Currently, third-party officials authorized by APHIS who
monitor treatments include operators of niger seed treatment
facilities, operators of wood packing material treatment facilities,
officials who monitor precooling treatment temperatures for cold
treatment, and others. As such, the provisions we proposed are more
inclusive than those currently in the regulations and reflect current
treatment activities; reverting to the original text would remove some
options for exporters. In addition, the provisions we proposed continue
to allow for preclearance or certification of treatment by the NPPO, as
appropriate. We have made no changes in response to these comments.
We also proposed to require treated commodities to be accompanied
by a phytosanitary certificate issued by the NPPO of the exporting
country certifying that treatment was conducted in accordance with
APHIS regulations when monitoring or certification of a treatment
involves an official authorized by APHIS. The current regulations
require phytosanitary certificates when treatment is monitored and
certified by an official of the exporting country. We proposed to
retain the requirement that the phytosanitary certificate be presented
to an inspector when the commodity is offered for entry into the United
States.
One commenter stated that it is inappropriate for the NPPO of the
exporting country to certify that a treatment has been conducted in
accordance with APHIS regulations if the treatment is not monitored by
an NPPO official. This commenter also noted that some treated
commodities are not required to be accompanied by phytosanitary
certificates.
When treatments are conducted in a foreign country, an NPPO
official is always involved in monitoring the treatment. However, the
commenter is correct that many articles whose importation is authorized
only if they are treated are not required to be accompanied by a
phytosanitary certificate; for example, regulated wood packaging
material is required under Sec. 319.40-3(b) to be treated before
importation, but a stamp on the wood packaging indicates that the
treatment has been conducted. Requirements that phytosanitary
certificates accompany imported articles are typically contained in
APHIS permits or in the regulations in 7 CFR part 319, which contains
requirements for importing various articles; it is not necessary to
include a separate phytosanitary certificate requirement for treated
articles in part 305, especially when there would be many exceptions to
that requirement. Therefore, we will not be finalizing the
phytosanitary certificate-related provisions discussed earlier that we
had proposed to include in Sec. 305.4(b).
Chemical Treatment
We proposed to retain the requirements for chemical treatment in
Sec. 305.5, with minor changes. Paragraph (a) of Sec. 305.5 requires
fumigation treatment facilities to be certified by APHIS and to be
inspected and recertified annually, or as often as APHIS directs,
depending upon treatments performed, commodities handled, and
operations conducted at the facility.
One commenter stated that, consistent with international
agreements, the NPPO of the exporting country is capable of testing
treatment facilities and certifying them as being capable of delivering
the treatments required by the importing country. The commenter stated
that this level of certification is not justified and presents a
significant logistical and cost burden on treatment facilities, while
not necessarily improving the quarantine security of consignments being
exported to the United States. The commenter suggested that, at most,
the certification be based on information submitted by the NPPO of the
exporting country that is sufficient to demonstrate that the
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facilities treating consignments are capable of meeting the
requirements of Sec. 305.5(a).
We did not propose to change the certification requirements for
fumigation treatment facilities, and we would want to allow the public
to comment on such a change before it was implemented. Therefore, we
have made no changes to these provisions in response to this comment.
However, we will consider the change the commenter suggested; if we
determine that it is warranted, we will publish a proposed rule
soliciting public comment on the change.
Cold Treatment
We proposed to move the requirements for cold treatment from Sec.
305.15 to Sec. 305.6, with minor changes. Paragraph (d)(6) of Sec.
305.15, which is identical to proposed Sec. 305.6(d)(6), has stated
that only the same type of fruit in the same type of package may be
treated together in a container; no mixture of fruits in containers may
be treated.
One commenter suggested that we define ``type.'' The commenter
stated that a ``type'' of fruit, for the purpose of cold treatment,
should be those fruits that are to be treated under the same schedule
and that belong to the same genus. The commenter stated that different
types of packaging might affect the delivery of cold treatment due to
issues associated with the circulation of cold air, but different
varieties of a particular species (such as Lisbon and Meyer lemons, or
Washington Navel and Valencia oranges) do not affect treatment
efficacy.
We agree with the commenter that varietal differences within a
species do not affect the efficacy of cold treatment. However, we have
determined that variations among species are significant enough that
only fruit of the same species should be treated together using
currently approved cold treatments; thus, we currently allow only fruit
of the same species to be treated together. That said, we may determine
in the future that a cold treatment schedule can be applied to fruit of
the same genus. For that reason, we are not adding a definition of
``type'' to the regulations, but we are adding guidance on the meaning
of ``type'' to the PPQ Treatment Manual. If we determine that a
schedule could be used for fruit of the same genus, we would then be
able to update the PPQ Treatment Manual to reflect that determination
through the notice-based process we are adding to the regulations in
this final rule.
This commenter also stated that, where the same treatment is
applied and the same packaging type is used, the inclusion of both
lemons and oranges in a single treatment container should not
necessarily be considered to invalidate the treatment, provided the
more stringent of the two available treatments is applied. The
commenter stated that these fruit are closely related, have a similar
structure, and would be predicted to have a similar rate of respiration
that would influence the cold treatment and the development of any
``hot spots'' in the treatment enclosure.
We believe that the commenter's suggestion has some potential
merit, but operational issues could make such a treatment process
difficult to implement. However, we will consider the change the
commenter suggested; if we determine that it is warranted, and that the
operational issues associated with such a change could be adequately
resolved, we will publish a proposed rule soliciting public comment on
the change.
Heat Treatment
We proposed to move the requirements for heat treatment from Sec.
305.20 to Sec. 305.8, with minor changes. Paragraph (a)(1) of Sec.
305.20, which is identical to proposed Sec. 305.8(a)(1), has stated
that a certified facility must have equipment that is capable of
adequately circulating air or water (as relevant to the treatment).
One commenter asked whether the interpretation of ``air'' in the
regulations would include steam or vapor. The commenter noted that
three main forms of heat treatment are generally accepted, hot water
immersion, high temperature forced air, and vapor heat treatment, and
suggested that the text of this section include the term ``air/vapor.''
Steam and vapor are simply phases of water and, as used in
treatments, are thus a mixture of air and water. As the regulations
include requirements for circulation of air and water, we have
determined that it is not necessary to further specify that facilities
must be able to adequately circulate vapor.
Irradiation
The regulations have contained three sections that set out
requirements for performing irradiation treatment: Sec. 305.31, for
irradiation treatment of imported regulated articles; Sec. 305.32, for
regulated articles moved interstate from areas quarantined for fruit
flies; and Sec. 305.34, for regulated articles moved interstate from
Hawaii, Puerto Rico, and the U.S. Virgin Islands. The requirements in
these sections were mostly similar, and some of them were identical. We
proposed to consolidate and harmonize the existing irradiation
requirements into one section that would set out irradiation
requirements for all articles for which irradiation is an authorized
treatment. We also proposed to make minor changes to the irradiation
treatment requirements.
One commenter stated that the irradiation treatment regulations
provide a much greater level of detail than the equivalent sections for
other treatments. The commenter asked whether it is necessary to
include this level of detail in the regulations, or whether it would be
beneficial to include much of this detail in either the PPQ Treatment
Manual or the other documentation specific to the irradiation
treatment, such as the irradiation treatment framework equivalency
workplan (FEWP). The commenter stated that reducing the level of detail
in the regulations to be consistent with the other treatments would
provide APHIS with more flexibility to amend the treatment requirements
in the future, rather than having to complete rulemaking to do so.
The level of detail we proposed to include in the regulations
reflects the level of detail that has been in the regulations. We did
not propose to change the provisions of the irradiation regulations
except as necessary to harmonize among the three sets of regulations
and to correct errors and inconsistencies. Based on the comments we
received, we will examine the irradiation regulations; if warranted, we
will publish a separate proposal to amend them by removing detail and
invite public comment on the proposal.
Two commenters stated that several requirements in the irradiation
treatment regulations are related specifically to fruit flies. One of
these commenters stated that the regulations contain requirements
related to packaging, labeling, movement, and facility location that
are specific to fruit flies and recommended that the regulations make
it clear that irradiation is approved for many pests other than fruit
flies.
The other commenter suggested that we review the proposed
regulations and replace references to fruit flies with references to
``pests of concern'' where appropriate. This commenter specifically
suggested that we change proposed Sec. 305.9(c)(1)(i), which relates
to compliance agreements for facilities treating imported articles in
the United States. As proposed, this paragraph indicated that, in the
facility compliance agreement, the facility operator must agree to
comply with any additional requirements found necessary by APHIS to
prevent the escape, prior to irradiation, of any fruit
[[Page 4232]]
flies that may be associated with the articles to be irradiated.
We agree with these commenters that the regulations should indicate
that irradiation can be used to treat pests other than fruit flies, as
irradiation is approved as a treatment for all pests of the class
Insecta, other than pupae and adults of the order Lepidoptera. The
proposed rule included several changes to the existing irradiation
requirements to refer to pests of concern rather than to fruit flies
specifically. In addition, we are taking the second commenter's
suggestion to replace the reference to fruit flies in proposed Sec.
305.9(c)(1)(i) with a reference to ``pests of concern.''
Some of the references to fruit flies in the regulations relate to
the fact that, for articles moved within the continental United States,
irradiation has only been approved as a treatment for articles moved
interstate from areas quarantined for fruit flies. However, under this
final rule, such facilities can treat any pest for which there is an
approved dose in the PPQ Treatment Manual. We did not propose to expand
the use of irradiation to facilities located in any areas quarantined
for other pests in the proposal, although we may do so in the future.
Of the requirements cited by the first commenter, only the facility
location requirements are specifically related to fruit flies. These
are discussed in further detail in response to the next comment.
However, the packaging, labeling, and movement requirements in the
regulations all act as general safeguards against pests of concern, and
the regulations as amended by this final rule reflect that.
Paragraph (a) of proposed Sec. 305.9 contained the facility
location requirements referred to earlier, which were taken from Sec.
305.31(b). Under the proposed requirements, for articles that are
imported or moved interstate from Hawaii or U.S. territories,
irradiation facilities may be located in any State on the mainland
United States except Alabama, Arizona, California, Florida, Kentucky,
Louisiana, Nevada, New Mexico, South Carolina, Tennessee, Texas, and
Virginia. In the States of Georgia, Mississippi, and North Carolina,
irradiation facilities may only be located at the maritime ports of
Gulfport, MS, or Wilmington, NC, or the airport of Atlanta, GA, and
only if certain special conditions are met. Those conditions are
designed to mitigate the risk of escape of fruit flies from the
facility.
One commenter stated that no reason for excluding those listed
States was included in the proposal and suggested that information on
why these States are excluded be added to the rule. The commenter
suggested that, if it is only Federal or State legislation that
prevents the use of irradiation facilities in those States for imported
commodities, the additional legislation could be referenced and the
specific list of States included only in the PPQ Treatment Manual,
rather than the regulations. This change, the commenter stated, would
prevent the need for a formal rule change should States be added to or
removed from the list.
The States listed in the regulations are States where fruit flies
could become established if introduced into the United States. We
exclude these States to safeguard against the possibility that, despite
the container and movement restrictions in the irradiation treatment
regulations, fruit flies could escape from regulated articles in the
United States prior to treatment. This rationale was given in the final
rule establishing the irradiation treatment regulations for imported
articles, which was published in the Federal Register and effective on
October 23, 2002 (67 FR 65016-65029, Docket No. 98-030-4). As the
relevant climatic conditions in these States are not expected to
change, removing this list from the regulations to facilitate future
changes in the list is not necessary.
One commenter noted that the regulations provide conditions for the
placement of a facility in the listed States at three specific ports of
entry. The commenter suggested that these provisions should not be in
the regulations but in the PPQ Treatment Manual. The commenter stated
that this type of detail, which might change based on specific
approvals, would be better handled within the PPQ Treatment Manual.
Amendments to the list could follow the same notice-and-comment process
we proposed for changes to the PPQ Treatment Manual.
We are considering rulemaking to establish conditions under which
facilities could be located in the States listed in paragraph (a) of
proposed Sec. 305.9. Should we decide to promulgate rulemaking to
establish such conditions, we would include the list of approved
facilities in the Treatment Manual, as the commenter suggests. However,
making such a change in this final rule would be beyond the scope of
the proposed rule.
The irradiation treatment regulations require that an irradiation
treatment facility be certified by APHIS. The proposal included this
requirement in paragraph (d) of proposed Sec. 305.9. For the initial
certification of a facility, the irradiation treatment regulations
require that an inspector make a personal inspection of the facility to
determine whether it complies with the irradiation treatment facility
requirements; the proposal included this requirement in paragraph (l)
of proposed Sec. 305.9.
One commenter stated that this level of certification is not
justified and presents a significant logistical and cost burden on
treatment facilities, while not necessarily improving the quarantine
security of consignments being exported to the United States. The
commenter stated that the key parts of the irradiation system are the
dose mapping system and the routine dosimetry system. Because the
regulations require these dosimetry systems to be compliant with the
International Standards Organization/American Society for Testing and
Materials (ISO/ASTM) standard or an equivalent standard recognized by
APHIS, the commenter stated that there should be no need for specific
certification visits by APHIS officials, provided that these standards
are met. In this case, the commenter suggested, APHIS could use audit
trails and certificates provided by accredited testing and
certification laboratories to determine whether the treatment facility
meets all the necessary requirements.
We have determined that, for the initial certification of a
facility, it is necessary to conduct a personal inspection to ensure
that the facility is in compliance with the ISO/ASTM standard. Audit
trails and certificates provided by accredited testing and
certification laboratories would not provide adequate assurance that
the facility is in compliance with the standard. In addition, while we
agree that the dose mapping and routine dosimetry systems are key
components of irradiation treatment, the regulations include many other
requirements that are necessary to ensure the phytosanitary security of
treated articles, such as provisions to separate treated and untreated
articles and to prevent the infestation of treated articles by
quarantine pests after treatment. The facility's systems and processes
to ensure compliance with these requirements also need to be verified
by a personal inspection. We are making no changes in response to this
comment.
The irradiation treatment regulations have referred to an increase
or decrease in the amount of radioisotope as an event because of which
recertification would be required. These events are found in the
introductory text of paragraph (d) of proposed Sec. 305.9. We proposed
to add the word ``significant'' to better characterize the type of
decrease that would require recertification, since radioisotope
decreases in very small amounts during
[[Page 4233]]
treatment; otherwise, we did not propose to change this requirement.
Two commenters stated that increases in the amount of isotope
should not necessitate recertification, and one stated that decreases
in the amount of isotope should not either. Both commenters stated that
if processes for maintaining the isotope have been established by the
facility and approved by APHIS, changes in isotope should not require
additional review by APHIS, except as necessary to confirm that the
processes are being properly implemented.
As noted, the requirement for recertification in the event of a
change in the amount of radioisotope has been found in all three sets
of irradiation treatment facility provisions; we did not propose to
change that requirement, other than making it more specific and thus
more clear regarding what events require recertification. We have
required recertification in the event of a change in the amount of
radioisotope in order to verify that the radioisotope is at a proper
level and treatment is being conducted in accordance with the ISO/ASTM
standard and the facility's standard operating procedures. As discussed
in more detail later in this document, it is especially important to
verify that irradiation treatment is being properly conducted. We are
making no changes in response to these comments.
However, we have determined that the proposed text could be more
specific in describing what decreases warrant recertification. This
final rule refers to a decrease in the amount of radioisotope for a
reason other than natural decay, rather than to a significant decrease
in the amount of radioisotope, as a reason for recertification. This
reflects the intent of the proposed change more specifically and
provides helpful additional information to the reader.
The irradiation treatment regulations require irradiation treatment
to be monitored by an inspector. Monitoring will include inspection of
treatment records and unannounced inspections of the facility by an
inspector, and may include inspection of articles prior to or after
irradiation. The proposal included these requirements in paragraph (e)
of proposed Sec. 305.9.
One commenter stated that such monitoring should not be required.
The commenter stated that monitoring and inspection of treatment
records can be performed by the NPPO of the exporting country. The
commenter also stated that specific provisions for inspection prior to
or after irradiation should not be included, as these should be
performed during or after the issuance of a phytosanitary certificate
by the NPPO of the exporting country.
We have determined that the current level of monitoring is
appropriate. Verifying that irradiation treatment is being applied
properly is particularly important because an inspector looking at
treated articles themselves after treatment would have no practical way
to determine, based on physical evidence from the commodity itself,
that the articles have been irradiated. Irradiation leaves no residue
and usually causes no discernable change to an article's color or
texture. In addition, as discussed earlier in this document, an
effective irradiation treatment may not kill all larvae, but instead
might prevent adult emergence. In cases where an inspector at the port
of entry encounters live larvae of the target pest in a shipment that
is documented as irradiated, it is extremely important that the
inspector be able to determine with full confidence that the article
was properly treated according to APHIS requirements. We are making no
changes in response to this comment.
One commenter stated that provisions in proposed paragraph (e)
imply that an inspector need not necessarily be present at all times
during treatment. However, the commenter stated, the requirement that
treatment ``must be monitored by an inspector'' will lead to some
confusion. The commenter suggested clarifying that an inspector may not
be required on site during treatment.
The commenter's interpretation that monitoring may or may not be on
site is correct. Immediately after the requirement the commenter cites,
the regulations go on to explain that monitoring will include
inspection of treatment records and unannounced inspections of the
facility by an inspector, and may include inspection of articles prior
to or after irradiation. If an unannounced visit is not being
conducted, monitoring would only necessarily include a review of
treatment records, which could be done off site. We believe the current
language is sufficiently clear on this point.
To ensure the appropriate level of monitoring for facilities
treating imported articles, the regulations in Sec. 305.31(f) have
required three agreements to be signed before articles can be imported
in accordance with the irradiation treatment requirements: An FEWP, a
facility preclearance workplan, and a trust fund agreement. We proposed
to move these requirements to proposed Sec. 305.9(e)(1). The only
change we proposed was to limit the applicability of these requirements
to facilities located in foreign countries, because ensuring that the
irradiation treatment requirements are met when monitoring irradiation
treatment in a foreign country involves an additional layer of
complexity. Such monitoring requires us to work with foreign
governments to ensure that all requirements are met, while monitoring
the irradiation treatment within the United States of imported articles
does not.
One commenter stated that, as specific details regarding the
inspection of irradiated articles are included in the FEWP and the
associated operational workplans, some of the specific details included
in proposed paragraph (e) are not necessary. Similarly, the commenter
suggested, as the extent of treatment oversight and monitoring would be
defined in the FEWP, the text of proposed paragraph (e)(1)(iii), which
contains the trust fund agreement requirements, could be simplified to
remove specific references to the duties undertaken by APHIS in the
exporting country.
The specific details the commenter cites are presented in the
regulations as examples and not as exhaustive lists. For example, the
requirements for the facility preclearance workplan that have been
found in Sec. 305.31(f)(2) and were proposed in Sec. 305.9(e)(1)(ii)
cite typical activities to be described in the workplan. These details
provide helpful additional detail to the reader. We are making no
changes in response to this comment.
Two commenters specifically addressed the FEWP. The regulations in
Sec. 305.31(f)(1), which we included in Sec. 305.9(e)(1)(i) of the
proposal, have required the NPPO of a country from which articles are
to be imported into the United States in accordance with the
irradiation treatment regulations to sign an FEWP with APHIS. In the
FEWP, both the NPPO and APHIS will specify the following items for
their respective countries:
Citations for any requirements that apply to the
importation of irradiated fruits and vegetables;
The type and amount of inspection, monitoring, or other
activities that will be required in connection with allowing the
importation of irradiated fruits and vegetables into that country; and
Any other conditions that must be met to allow the
importation of irradiated fruits and vegetables into that country.
One commenter suggested that we revise these requirements to simply
state that APHIS maintains the right to either deny the application
for, or retract the approval of, an operational workplan for an
irradiation facility if the
[[Page 4234]]
NPPO of the exporting country refuses to allow the importation of
articles treated with irradiation. The commenter stated that such
language would grant APHIS the legal right to determine equitable
reciprocity and take appropriate action. The commenter stated that, in
the case of domestic irradiation facilities that do not involve
operational workplans with foreign NPPOs, reciprocity should not be
required.
Another commenter requested that the requirement for the FEWP be
removed. This commenter stated that the requirement for the FEWP was
not based on science and thus constituted an unjustified barrier to
trade. Because the requirement for the FEWP is not based on science,
the commenter stated, APHIS is not authorized to impose such a
requirement under the Plant Protection Act (7 U.S.C. 7701 et seq.),
which states that decisions affecting imports, exports, and interstate
movement of regulated products shall be based on sound science. The
commenter stated that the requirement for the FEWP was causing costly
delays in attempts by the commenter's business to establish a facility
for irradiating products for export to the United States, as the
government of the country in which the facility is intended to be
located is reluctant to take the steps that government has determined
to be necessary to agree to an FEWP.
The FEWP was originally established in the irradiation regulations
to support the equivalence principle of the WTO Agreement on the
Application of Sanitary and Phytosanitary Measures by clearly stating
what legislative, regulatory, and other requirements must be met, and
what monitoring and other activities must occur, for irradiated
articles to be imported into the United States, or into the foreign
country. We did not propose to change the provisions required to be
included in the FEWP requirements.
The FEWP does not obligate the government of a country in which an
irradiation facility is located to agree to any specific conditions for
the use of irradiation as a phytosanitary measure, but merely to
document the conditions under which irradiated articles can be imported
into that country. We will provide clarification regarding this point
to any country that is encountering difficulty in preparing an FEWP.
As noted above, we proposed to change the FEWP requirement so that
it only applied to facilities located outside the United States.
However, upon further considering the purpose of the FEWP, we have
determined that the FEWP should continue to be required for all
facilities treating imported articles, whether located outside or
inside the United States, as the equivalence principle applies
regardless of where imported articles are treated. Therefore, this
final rule contains the FEWP requirement in a separate paragraph (e)(1)
that applies to all facilities treating imported articles. Paragraph
(e)(2) contains the remaining requirements for facilities located in
foreign countries, and paragraph (e)(3) contains the requirements for
facilities located in the United States; the latter paragraph refers to
the FEWP requirement in paragraph (e)(1) for facilities located in the
United States that are treating imported articles.
With regard to the first commenter's suggestion, the current FEWP
provisions provide helpful additional specificity regarding what
information about the exporting country's irradiation requirements
needs to be conveyed in order for equivalence to be established. We are
making no changes in response to this comment.
Two commenters specifically addressed the facility preclearance
workplan. Prior to commencing importation into the United States of
articles treated at a foreign irradiation facility, APHIS and the NPPO
of the country from which articles are to be imported must jointly
develop a preclearance workplan that details the activities that APHIS
and the foreign NPPO will carry out in connection with each irradiation
facility to verify the facility's compliance with the irradiation
treatment requirements of this section. Typical activities to be
described in this workplan may include frequency of visits to the
facility by APHIS and foreign plant protection inspectors, methods for
reviewing facility records, and methods for verifying that facilities
are in compliance with the requirements for separation of articles,
packaging, labeling, and other irradiation treatment requirements. This
facility preclearance workplan will be reviewed and renewed by APHIS
and the foreign NPPO on an annual basis.
Both commenters stated that preclearance should not be mandatory in
all cases and that this specific workplan should be renamed. One
commenter suggested calling it the ``treatment facility workplan,'' and
the other suggested the ``irradiation facility workplan.'' The latter
commenter stated that making this change would allow the flexibility to
move from a preclearance program to one in which treatments are
monitored by officials authorized by APHIS and the commodity is shipped
with a phytosanitary certificate issued by the NPPO of the exporting
country, given sufficient evidence regarding the success of the
program.
We assume that the commenters are referring to ``preclearance'' as
the activity in which APHIS inspectors are present in a foreign country
and conduct inspections there prior to export of the inspected
articles. That is how APHIS has commonly used the term in developing
export programs for particular articles. However, the regulations for
irradiation treatment facilities use ``preclearance'' in a different
sense, to refer to preclearing treatments conducted at the facility.
Because inspectors monitor treatment, there is no additional
verification of the treatment that needs to be done at the port of
entry, which is important given that there is no practical way to
verify treatment, as discussed earlier.
However, articles treated in a precleared facility are not
necessarily themselves precleared. Irradiated articles may be subject
to mitigations besides irradiation treatment for certain pests. For
example, litchi from Thailand are required by Sec. 319.56-47 to be
treated with irradiation for several insect pests and also to be
inspected by the Thai NPPO and found to be free of the fungus
Peronophythora litchi, which is not neutralized by irradiation
treatment. Thus, litchi from Thailand are not precleared for entry into
the United States, even though the irradiation treatment facility in
which they are treated is precleared.
As discussed earlier, we need to retain the facility preclearance
workplan in support of our monitoring requirements, given the
difficulty associated with verifying that irradiation has been
conducted properly. As the regulations refer specifically to a
``facility preclearance workplan'' and not a general preclearance
workplan, we do not believe any further change is necessary to indicate
that the preclearance discussed applies to treatments conducted in the
facility and not necessarily to any articles treated by the facility.
The regulations have required in Sec. Sec. 305.32(b) and
305.34(b)(3) that facilities located within the United States that
carry out continual irradiation operations notify an inspector at least
24 hours before the date of operations, while facilities that carry out
periodic irradiation operations must notify an inspector of scheduled
operations at least 24 hours before scheduled operations. This
requirement
[[Page 4235]]
was included in Sec. 305.9(e)(2) of the proposal.
One commenter stated that what is meant by ``continual'' and
``periodic'' operations is not clear. The commenter suggested that we
either clarify or simply change the proposed text from ``...before the
date of operations...'' to ``...before the date of initial
operations....''.
Re-examining the current requirements, we note that an inspector
must be notified 24 hours before scheduled operations regardless of
whether operations are continual or periodic. Therefore, as the
commenter suggests, we have simplified this requirement in the final
rule by eliminating distinctions between the two types of facilities.
In order to ensure that inspectors have adequate notice, we are
also clarifying this provision to indicate that the notification must
come at least 24 hours, excluding Saturday, Sunday, and Federal
holidays, before scheduled operations, so that notification for
irradiation that is scheduled for the next Monday does not arrive on a
Saturday, a Sunday, or a Federal holiday, which are not standard
business days for APHIS inspectors. The provision thus reads as follows
in this final rule: ``Facilities located within the United States must
notify an inspector at least 24 hours (excluding Saturday, Sunday, and
Federal holidays) before scheduled operations.''
Paragraph (f) of proposed Sec. 305.9 contained the packaging
requirements of the irradiation treatment regulations. Paragraph (f)(2)
contained requirements for packaging articles that are irradiated prior
to arrival in the United States, prior to interstate movement from
Hawaii or U.S. territories, and prior to movement from an area
quarantined for fruit flies. The regulations for irradiation treatment
of articles moved interstate from Hawaii and U.S. territories and from
quarantined areas only allow irradiated articles to be packaged in
insect-proof cartons. The regulations for irradiation treatment of
imported articles allow either insect-proof cartons or noninsect-proof
cartons to be used; if noninsect-proof cartons are used, the cartons
must be stored immediately after irradiation in a room completely
enclosed by walls or screening that completely precludes access by the
pests of concern. If stored in noninsect-proof cartons in a room that
precludes access by the pests of concern, prior to leaving the room,
each pallet of cartons must be completely enclosed in polyethylene
shrink wrap, or another solid or netting covering that completely
precludes access to the cartons by the pests of concern. We proposed in
Sec. 305.9(f)(2)(i)(B) to allow the use of noninsect-proof cartons,
subject to these conditions, for articles moved interstate from areas
quarantined for fruit flies and from Hawaii and U.S. territories as
well.
One commenter expressed uncertainty regarding whether the complete
enclosure of the pallet in polyethylene shrink wrap or other covering
should include the underside of the product and, if so, how one can
shrink wrap all six sides of a pallet of product.
If the bottom of a pallet was insect-proof, we would not require
the bottom of the pallet to be wrapped in polyethylene shrink wrap. The
requirements for the use of noninsect-proof cartons are satisfied if
access to the pallet is precluded by polyethylene shrink wrap or solid
or netting covering.
One commenter stated that the requirement to wrap pallets of
noninsect-proof cartons to prevent access by the pests of concern may
be an appropriate safeguarding measure for articles transported by air,
since the pallets are almost always exposed during the loading of the
aircraft, but is not appropriate for maritime shipments, when the
pallets of treated articles are loaded directly into the maritime
container at the packing shed under adequate safeguards and
subsequently sealed by the inspector or by another official authorized
by APHIS. The commenter suggested that proposed Sec. 305.9(f)(2)(i)(B)
be reworded to make a distinction between requirements for air and
maritime shipment, as is the case in other programs such as the program
for hot water treatment of mango, and incorporated into the PPQ
Treatment Manual rather than remain in the regulations.
The intent of this requirement is to prevent the treated articles
from being reinfested by the pests of concern after treatment. As
articles are exposed to potential pest infestation while they are being
loaded into maritime containers, it is necessary to include a
requirement to address this risk for maritime shipments as well.
Although the mango hot water treatment program allows for such loading
to be conducted without wrapping the mangoes, as noted earlier, it is
much more difficult for an inspector at a port of entry to verify that
an article has been treated with irradiation; in contrast, an inspector
could easily determine that live fruit flies in mangoes that have been
treated with hot water represented a failure of either the treatment or
the post-treatment safeguarding and take appropriate action. We will
consider whether providing for supervision of the maritime transloading
process might adequately mitigate this risk; if we determine that it
would, we would propose rulemaking to provide for such supervision, and
take public comment on the change.
The regulations in Sec. Sec. 305.31(g)(3)(ii), 305.32(c)(2), and
305.34(b)(4)(i)(B) have required each pallet-load of cartons containing
irradiated articles to be wrapped before leaving the irradiation
facility in one of the following ways:
With polyethylene shrink wrap;
With net wrapping; or
With strapping so that each carton on an outside row of
the pallet load is constrained by a metal or plastic strap.
We included this requirement in Sec. 305.9(f)(2)(ii) of the
proposal.
One commenter stated an assumption that the concern of proposed
paragraph (f)(2)(ii) is to ensure that pallets do not topple and that
nontreated cartons cannot be inserted into pallets of treated articles.
The commenter suggested that we substitute the word ``secured'' for the
word ``wrapped,'' as it more accurately describes the process when
cornices and strapping are used to stabilize the pallet. The commenter
also stated that requiring the strapping to pass and constrain each
carton on the outside row of the pallet load exceeds current industry
practices and would increase operational costs. The commenter suggested
that the requirement be reworded to indicate that pallet loads should
be secured by shrink wrap, netting, or strapping, without specifying
how the strapping is to be applied.
We agree with the commenter's suggestions. Accordingly, Sec.
305.9(f)(2)(ii) in this final rule uses the word ``secured'' rather
than the word ``wrapped,'' and does not include specific instructions
on how to use strapping to secure the pallet.
In addition, the packaging requirements for sweetpotatoes moved
interstate from Hawaii in Sec. 318.13-25 are similar to the packaging
requirements for irradiated articles, and contain identical
requirements for wrapping pallets; we are also changing those
requirements in this final rule, to be consistent with the changes we
are making in the irradiation regulations.
The regulations in Sec. Sec. 305.31(g)(3)(iii), 305.32(c)(3), and
305.34(b)(4)(i)(C) have required packaging to be labeled with treatment
lot numbers, packing and treatment facility identification and
location, and dates of packing and treatment. We included this
requirement in Sec. 305.9(f)(2)(ii) of the proposal.
One commenter stated that this level of detail does not need to be
included in the regulations and that it would be
[[Page 4236]]
preferable for the regulations to only state that the packaging be
labeled in such a way as to enable the necessary level of traceback.
The inclusion of any identifying mark on the packaging that would
permit APHIS to correlate the specific shipment to a treatment
certificate, import permit, or other system would provide an equivalent
level of traceback. As this detail already exists in the draft
operational workplans, the commenter suggested that the principle of
traceback be mentioned in paragraph (f)(2)(iii) without specifically
requiring treatment facility codes, dates, or other information. As the
operational workplans will be more easily amended than the regulations,
the commenter stated that this option would allow APHIS to more easily
take into consideration the specific systems in the exporting country.
We agree with the commenter's suggestion. In this final rule,
paragraph (f)(2)(iii) specifies that packaging must be labeled in a
manner that allows an inspector to determine treatment lot numbers,
packing and treatment facility identification and location, and dates
of packing and treatment. This ensures that the information necessary
to conduct traceback is available while allowing flexibility in
providing that information. We will approve packaging to be used at a
specific facility or for a specific commodity as part of the
development of the operational workplan for the facility.
In addition, the labeling requirements for sweetpotatoes moved
interstate from Hawaii in Sec. 318.13-25 contain similar requirements
for labeling cartons; we are also changing those requirements in this
final rule, to be consistent with the changes we are making in the
irradiation regulations.
One commenter suggested that APHIS change the wording (``Treated by
irradiation'' or ``Treated with radiation'') that must be stamped or
pre-printed on each carton to indicate that the articles were
irradiated to mitigate pest risks.
The wording is required by the Food and Drug Administration in its
regulations at 21 CFR 179.26(c). We have no authority to make changes
to those regulations.
Paragraph Sec. 305.31(h) has required containers or vans that will
transport treated commodities to be free of pests prior to loading the
treated commodities. We proposed to include this requirement in Sec.
305.9(g) and to make it applicable not only to facilities treating
imported articles but to facilities treating articles moved interstate
from Hawaii and U.S. territories and from areas quarantined for fruit
flies as well.
One commenter requested clarification on this requirement. The
commenter asked:
Whether the intent was to prevent infestation by pests of
concern or hitchhikers;
Whether the requirement applies to product treated in an
area where the pest(s) of concern are present, other areas, or both;
If articles are treated in a domestic facility, why it is
important that the container or van be pest-free after the product has
been processed; and
If the pests are not pests of concern, whether freedom
would need to be established inside the container or outside the
container.
The intent of the requirement is to prevent infestation by pests of
concern. The requirement applies regardless of whether pests of concern
are present in the area in which the articles are treated. Ensuring
that containers are free of pests of concern is a basic safeguarding
principle; for example, even if an irradiation facility was located in
an area free of pests of concern, a container could have been used to
carry infested articles, improperly cleaned, and brought to the
irradiation facility to contain treated articles.
To clarify this requirement, we are changing proposed Sec.
305.9(g) to refer specifically to pests of concern. We are also
changing proposed Sec. 305.9(g) to refer to ``articles,'' rather than
``commodities,'' as the term ``articles'' is used throughout Sec.
305.9.
Proposed paragraph (l) of Sec. 305.9 set out requirements for
requesting certification and inspection of a facility. These
requirements were taken from Sec. 305.31(l); similar requirements are
contained in Sec. Sec. 305.32(g) and 305.34(c). Each of these
paragraphs provides that, before the Administrator determines whether
an irradiation facility is eligible for certification, an inspector
will make a personal inspection of the facility to determine whether it
complies with the regulations.
One commenter asked whether this paragraph also applied to
recertification and, if so, suggested that we change this requirement
to indicate that an inspector may make a personal inspection, rather
than that an inspector will make a personal inspection. The commenter
stated that a minor technical reason for recertification should not
obligate APHIS to perform a personal inspection of the facility.
The requirements in proposed paragraph (l) apply only to the
initial certification of a facility, not to recertification. We have
added references to initial certification to paragraph (l) to make this
more clear.
We are also changing paragraph (n) of proposed Sec. 305.9, which
informs the reader that the Department is not responsible for damage to
treated articles and is taken from current Sec. Sec. 305.31(n),
305.32(i), and 305.34(e). This paragraph refers to ``listed plant
pests,'' which we are updating to refer to ``plant pests listed in the
PPQ Treatment Manual.'' It also refers to fruits and vegetables being
authorized for treatment; however, since articles other than fruits and
vegetables are authorized for treatment, ``articles'' is a more
appropriate term, and we are changing paragraph (n) accordingly.
Miscellaneous Changes
One commenter pointed out two typographical errors in the proposed
rule:
In proposed Sec. 305.6(b), the text ``and located in the
area north of 39[deg] longitude and east of 104[deg] latitude'' should
read ``and located in the area north of 39[deg] latitude and east of
104[deg] longitude''.
The section for quick freeze treatments was listed in the
regulatory text of the proposed rule as being Sec. 305.8. The
commenter pointed out that the section number should be Sec. 305.7.
We have corrected both of these errors in the final rule.
We are making two other miscellaneous changes to the proposed rule.
We proposed to remove the chemical treatment schedules in the appendix
to the subpart for imported fire ant (Sec. Sec. 301.81 through 301.81-
10), retaining only the systems approach for ensuring nursery freedom
from imported fire ant in a new Sec. 301.81-11. This systems approach
refers to treatment at 180-day intervals. However, as treatments for
the imported fire ant are added or changed, different intervals may be
required for treatment. To add flexibility to the systems approach, we
are changing the references to 180-day intervals in proposed Sec.
301.81-11 to refer instead to ``the specified number of days'' and
``the specified interval.''
Proposed Sec. 305.6(c) set out the requirements for cold treatment
enclosures that have been found in Sec. 305.15(c). Proposed paragraph
(c)(2) indicated that such enclosures must maintain fruit pulp
temperatures according to treatment schedules with no more than a 0.39
[deg]C (0.7 [deg]F) variation in temperature. This is related to a
requirement for performing cold treatment that we proposed to include
in Sec. 305.6(d)(9), which requires fruit pulp temperatures to be
maintained at
[[Page 4237]]
the temperature specified in the treatment schedule with no more than a
0.39 [deg]C (0.7 [deg]F) variation in temperature between two
consecutive hourly readings. To make these requirements consistent and
strengthen the connection between them, we are changing paragraph
(c)(2) in this final rule to indicate that the cold treatment enclosure
must maintain fruit pulp temperatures with no more than the specified
variation between two consecutive hourly readings as well.
Therefore, for the reasons given in the proposed rule and in this
document, we are adopting the proposed rule as a final rule, with the
changes discussed in this document.
Executive Order 12866 and Regulatory Flexibility Act
This final rule has been determined to be not significant for the
purposes of Executive Order 12866 and, therefore, has not been reviewed
by the Office of Management and Budget.
In accordance with the Regulatory Flexibility Act, we have analyzed
the potential economic effects of this action on small entities.
APHIS is amending 7 CFR parts 301, 305, 318, and 319 to streamline
the process for adding, revising, and removing treatment schedules and
for authorizing the use of existing treatments for additional
commodities. As required by the Regulatory Flexibility Act, we have
evaluated the potential economic effects of this action on small
businesses, small organizations, and small governmental jurisdictions
The regulations in 7 CFR chapter III are intended, among other
things, to prevent the introduction or dissemination of plant pests and
noxious weeds into or within the United States. Under the regulations,
certain plants, fruits, vegetables, and other articles must be treated
before they may be moved into the United States or interstate. The
phytosanitary treatments regulations contained in part 305 set out
standards and schedules for treatments required in parts 301, 318, and
319 for fruits, vegetables, and other articles.
APHIS is amending the phytosanitary treatment regulations in 7 CFR
part 305 by removing the lists of approved treatments and treatment
schedules from the regulations, while retaining the general
requirements for performing treatments and certifying or approving
treatment facilities. We are removing treatment schedules from other
places where they are currently found in 7 CFR chapter III as well.
Approved treatment schedules will instead be found in the PPQ Treatment
Manual, which is available on the Internet. We are also establishing a
new process to provide the public with notice and the opportunity to
comment on changes to treatment schedules. Finally, we are harmonizing
and combining the requirements for performing irradiation treatment for
imported articles, articles moved interstate from Hawaii and U.S.
territories, and articles moved interstate from an area quarantined for
fruit flies. These changes will simplify and expedite our processes for
adding, changing, and removing treatment schedules while continuing to
provide for public participation in the process. These changes will
also simplify our presentation of treatments to the public by
consolidating all treatments into one document and eliminating
redundant text from the regulations.
Eliminating the need for specific prior rulemaking for approving
new treatments or treatment schedules or for revising existing ones
under the notice-based process could result in considerable time
savings. The rulemaking process is an inherently longer process than a
notice-based process. Additionally, establishing a notice-based process
for approving new treatments or treatment schedules will facilitate use
of the already-established notice-based process for authorizing the
importation of fruits and vegetables set out in Sec. 319.56-4. Under
Sec. 319.56-4, APHIS can authorize the importation of fruits and
vegetables via a notice-based process if APHIS makes the determination
that the application of one or more designated phytosanitary measures
is sufficient to mitigate the risk that plant pests or noxious weeds
could be introduced into or disseminated within the United States via
the imported fruits or vegetables. Currently, however, if one of the
prescribed designated measures is a treatment that requires an
amendment to part 305, rulemaking is still required to amend the lists
of approved treatments or treatment schedules. Establishing a notice-
based process to amend the lists of approved treatments or treatment
schedules will streamline this process.
Consumers benefit from the opportunity to consume commodities from
a variety of sources, foreign as well as domestic. Consumer
expenditures for fruit and vegetables are growing faster than for any
food group other than meats. In many cases, fruit and vegetable imports
can occur only after those commodities have been treated to prevent the
introduction or movement of plant pests. This final rule will allow
treatments to be put in use more quickly when treatment changes are
necessary and when existing treatments are applied to new commodities;
treated products would become available to meet consumer demand sooner
than at present. Treated imports supplement domestic supplies,
especially of fresh products during the winter. Treatments also allow
for movement of domestically produced products to markets around the
country that otherwise would not occur. This movement results in
increased choices for consumers. Even where new imports compete
directly with domestic production, consumers benefit when increased
competition results in lower prices.
Those entities most likely to be affected by the rule are domestic
importers and producers of plants and plant products. The Small
Business Administration (SBA) has established guidelines for
determining which establishments are to be considered small. Import/
export merchants, agents, and brokers are identified within the broader
wholesaling trade sector. A firm primarily engaged in wholesaling is
considered small if it employs not more than 100 persons. In 2002, more
than 96 percent of fresh fruit and vegetable merchant wholesalers, more
than 99 percent of grain and field bean merchant wholesalers, and more
than 98 percent of flower and nursery stock wholesalers were considered
small by SBA standards.\4\ All types of farms are considered small if
they have annual receipts of $0.75 million or less. In 2002, more than
99 percent of oilseed and grain farms, more than 99 percent of
vegetable and melon farms, more than 99 percent of fruit and tree nut
farms, more than 99 percent of greenhouse, nursery, and floriculture
producers, and more than 99 percent of other crop farms were considered
small by SBA standards.\5\
---------------------------------------------------------------------------
\4\ 2002 Economic Census. Department of Commerce. U.S. Bureau of
the Census. North American Industry Classification System (NAICS)
Categories. 424480: Fresh fruit & Vegetable merchant wholesalers;
424510: Grain & field bean merchant wholesalers; 424930: Flower,
nursery stock, and florists' supplies merchant wholesalers.
\5\ 2002 Census of Agriculture. U.S. Department of Agriculture.
National Agricultural Statistics Service. NAICS Categories. 1111:
Oilseed & Grain farming; 1112: Vegetable and melon farming; 1113:
Fruit and tree nut farming; 1114: Greenhouse, nursery & Floriculture
production; and 1119: Other Crop farming.
---------------------------------------------------------------------------
Treatments are applicable to a wide variety of products including
fruits, vegetables, live plants, bulbs, seeds, grains, logs, lumber,
and other plants and plant products in a wide variety of circumstances.
Vast quantities of treated products move into and through the United
States annually. The United States is among the top producers and
[[Page 4238]]
consumers of plants and plant products. U.S. per-capita use of fruit
and tree nuts totals nearly 300 pounds each year, ranking third in per-
capita consumption of major food groups, next to dairy and vegetables.
Oranges, apples, grapes, and bananas are the most popular fruit while
almonds, pecans, and walnuts are the most preferred tree nuts. Annual
per capita use of all vegetables and melons averaged 445 pounds during
the first 5 years of the 2000s.
Table 1.--U.S. production value of selected crops, 2004-2006 ($ million)
----------------------------------------------------------------------------------------------------------------
Item 2004 2005 2006
----------------------------------------------------------------------------------------------------------------
Field and miscellaneous crops: ...................... ...................... ......................
----------------------------------------------------------------------------------------------------------------
Cotton, tobacco, sugar 8,674 8,702 8,648
----------------------------------------------------------------------------------------------------------------
Dry beans, peas, lentils 596 650 637
----------------------------------------------------------------------------------------------------------------
Grains, hay 47,367 45,225 57,209
----------------------------------------------------------------------------------------------------------------
Oilseeds 20,115 19,681 22,412
----------------------------------------------------------------------------------------------------------------
Potatoes, misc. 4,054 4,472 4,731
----------------------------------------------------------------------------------------------------------------
Fruit and nuts: ...................... ...................... ......................
----------------------------------------------------------------------------------------------------------------
Apples, pears 1,696 1,969 2,567
----------------------------------------------------------------------------------------------------------------
Berries 2,082 2,300 2,668
----------------------------------------------------------------------------------------------------------------
Citrus 2,485 2,303 2,738
----------------------------------------------------------------------------------------------------------------
Grapes 3,010 3,494 3,304
----------------------------------------------------------------------------------------------------------------
Nuts, other noncitrus 4,047 4,784 4,132
----------------------------------------------------------------------------------------------------------------
Stone fruit 1,243 1,462 1,563
----------------------------------------------------------------------------------------------------------------
Fresh vegetables: ...................... ...................... ......................
----------------------------------------------------------------------------------------------------------------
Brassica 1,111 1,118 1,225
----------------------------------------------------------------------------------------------------------------
Lettuce, spinach 2,062 2,108 2,635
----------------------------------------------------------------------------------------------------------------
Melons 728 873 877
----------------------------------------------------------------------------------------------------------------
Onions, peppers 1,300 1,501 1,674
----------------------------------------------------------------------------------------------------------------
Tomatoes 2,445 2,609 2,670
----------------------------------------------------------------------------------------------------------------
Other vegetables 1,430 1,599 1,619
----------------------------------------------------------------------------------------------------------------
In 2006, U.S. production of field and miscellaneous crops was
valued at more than $93 billion, with grains, hay, and oilseeds
accounting for the majority of this value. Fruit and tree nuts
production was valued at about $17 billion. More than 63 percent of
this production was in grapes, apples, almonds, oranges, and
strawberries. Commercial vegetable production for the fresh market was
valued at almost $11 billion, with tomatoes, lettuce, onions, broccoli,
and sweet corn accounting for about 60 percent of this value.
Imports have become increasingly important for domestic
consumption. Imports of plants and plant products have expanded rapidly
over the past two decades, and include many new and newly traded
commodities. In 2006, the United States imported approximately $5.8
billion in fresh fruits and tree nuts, about $2.5 billion in fresh
vegetables, and about $1.5 billion in live plants and other plant
products. Logs, lumber, and other timber product imports were valued at
nearly $12 billion in 2006.
Table 2.--U.S. imports of plants and plant products, 2004-2006 ($ million)
----------------------------------------------------------------------------------------------------------------
Item 2004 2005 2006
----------------------------------------------------------------------------------------------------------------
Live plants, bulbs, etc.: ........................ ...................... .......................
----------------------------------------------------------------------------------------------------------------
Bulbs, tubers 208 208 208
----------------------------------------------------------------------------------------------------------------
Cut flowers, dried 706 709 768
----------------------------------------------------------------------------------------------------------------
Foliage 102 114 123
----------------------------------------------------------------------------------------------------------------
Other live plants 362 352 358
----------------------------------------------------------------------------------------------------------------
[[Page 4239]]
Fruit and nuts: ........................ ...................... .......................
----------------------------------------------------------------------------------------------------------------
Bananas 1,102 1,134 1,201
----------------------------------------------------------------------------------------------------------------
Citrus, fresh 307 356 407
----------------------------------------------------------------------------------------------------------------
Coconuts, Brazil nuts 640 660 602
----------------------------------------------------------------------------------------------------------------
Dates, figs, pineapples 570 812 936
----------------------------------------------------------------------------------------------------------------
Grapes 743 980 953
----------------------------------------------------------------------------------------------------------------
Other fruits and nuts 1,127 1,174 1,297
----------------------------------------------------------------------------------------------------------------
Fresh vegetables: ........................ ...................... .......................
----------------------------------------------------------------------------------------------------------------
Cucumbers, gherkins 349 319 421
----------------------------------------------------------------------------------------------------------------
Melons 369 393 431
----------------------------------------------------------------------------------------------------------------
Onions, shallots 254 308 282
----------------------------------------------------------------------------------------------------------------
Tomatoes 1,054 1,075 1,234
----------------------------------------------------------------------------------------------------------------
Other vegetables 417 508 543
----------------------------------------------------------------------------------------------------------------
Logs, lumber, and other timber ........................ ...................... .......................
products:
----------------------------------------------------------------------------------------------------------------
Wood in the rough 246 348 347
----------------------------------------------------------------------------------------------------------------
Wood, sawn or chipped 8,799 8,989 8,333
----------------------------------------------------------------------------------------------------------------
Other wood 2,894 3,074 3,235
----------------------------------------------------------------------------------------------------------------
While treatments are applicable to a wide variety of plants and
plant products in a wide variety of circumstances, the changes in this
final rule will not alter current treatment requirements, the manner in
which new treatments are evaluated, or when and how treatments are
ultimately used other than in emergency situations. The final rule will
allow treatment changes to be implemented more rapidly and therefore
facilitate the movement of treated products to meet consumer demand.
These changes are not expected to significantly impact the total supply
of plants and plant products in the United States. Therefore, we expect
at most small effects on U.S. marketers and consumers.
Under these circumstances, the Administrator of the Animal and
Plant Health Inspection Service has determined that this action will
not have a significant economic impact on a substantial number of small
entities.
Executive Order 12372
This program/activity is listed in the Catalog of Federal Domestic
Assistance under No. 10.025 and is subject to Executive Order 12372,
which requires intergovernmental consultation with State and local
officials. (See 7 CFR part 3015, subpart V.)
Executive Order 12988
This final rule has been reviewed under Executive Order 12988,
Civil Justice Reform. This rule: (1) Has no retroactive effect and (2)
does not require administrative proceedings before parties may file
suit in court challenging this rule.
Paperwork Reduction Act
This final rule contains no new information collection or
recordkeeping requirements under the Paperwork Reduction Act of 1995
(44 U.S.C. 3501 et seq.).
List of Subjects
7 CFR Part 301
Agricultural commodities, Plant diseases and pests, Quarantine,
Reporting and recordkeeping requirements, Transportation.
7 CFR Part 305
Agricultural commodities, Chemical treatment, Cold treatment, Heat
treatment, Imports, Irradiation, Phytosanitary treatment, Plant
diseases and pests, Quarantine, Quick freeze, Reporting and
recordkeeping requirements, Transportation.
7 CFR Part 318
Cotton, Cottonseeds, Fruits, Guam, Hawaii, Plant diseases and
pests, Puerto Rico, Quarantine, Transportation, Vegetables, Virgin
Islands.
7 CFR Part 319
Coffee, Cotton, Fruits, Imports, Logs, Nursery stock, Plant
diseases and pests, Quarantine, Reporting and recordkeeping
requirements, Rice, Vegetables.
7 CFR Part 330
Customs duties and inspection, Imports, Plant diseases and pests,
Quarantine, Reporting and recordkeeping requirements, Transportation.
7 CFR Part 352
Customs duties and inspection, Imports, Plant diseases and pests,
Quarantine, Reporting and recordkeeping requirements, Transportation.
0
Accordingly, we are amending 7 CFR chapter III as follows:
[[Page 4240]]
PART 301--DOMESTIC QUARANTINE NOTICES
0
1. The authority citation for part 301 continues to read as follows:
Authority: 7 U.S.C. 7701-7772 and 7781-7786; 7 CFR 2.22, 2.80,
and 371.3.
Section 301.75-15 issued under Sec. 204, Title II, Public Law
106-113, 113 Stat. 1501A-293; sections 301.75-15 and 301.75-16
issued under Sec. 203, Title II, Public Law 106-224, 114 Stat. 400
(7 U.S.C. 1421 note).
0
2. In Sec. 301.32-10, in the introductory text, the first sentence is
revised to read as follows:
Sec. 301.32-10 Treatments.
Regulated articles may be treated in accordance with part 305 of
this chapter to neutralize fruit flies. * * *
* * * * *
Sec. 301.50-5 [Amended]
0
3. In Sec. 301.50-5, paragraph (a)(1)(i) is amended by removing the
citation ``Sec. 301.50-10(d)'' and adding the citation ``Sec. 301.50-
10(b)'' in its place.
0
4. Section 301.50-10 is amended as follows:
0
a. By revising paragraph (a) to read as set forth below.
0
b. By removing paragraphs (b) and (c).
0
c. By redesignating paragraph (d) as paragraph (b).
Sec. 301.50-10 Treatments and management method.
(a) Regulated articles may be treated in accordance with part 305
of this chapter to neutralize the pine shoot beetle.
* * * * *
Sec. 301.75-4 [Amended]
0
5. In Sec. 301.75-4, paragraph (d)(2)(i)(C) is amended by removing the
words ``Sec. 301-11(d) of this subpart'' and adding the words ``part
305 of this chapter'' in their place; paragraphs (d)(2)(ii)(C),
(d)(2)(ii)(D), (d)(2)(ii)(E), and (d)(4) are amended by removing the
words ``Sec. 301.75-11(d) of this subpart'' and adding the words
``part 305 of this chapter'' in their place; and paragraph (d)(4) is
amended by removing the words ``Sec. 301.75-11(c) of this subpart''
and adding the words ``part 305 of this chapter'' in their place.
Sec. 301.75-6 [Amended]
0
6. In Sec. 301.75-6, paragraphs (b)(5) and (b)(6) are amended by
removing the words ``Sec. 301.75-11(d)'' and adding the words ``part
305 of this chapter'' in their place; and paragraph (b)(5) is amended
by removing the words ``Sec. 301.75-11(c)'' and adding the words
``part 305 of this chapter'' in their place.
Sec. 301.75-7 [Amended]
0
7. In Sec. 301.75-7, paragraph (a)(2) is amended by removing the
citation ``Sec. 301.75-11(a)'' and adding the words ``part 305 of this
chapter'' in its place.
Sec. 301.75-8 [Amended]
0
8. In Sec. 301.75-8, paragraph (b) is amended by removing the words
``Sec. 301.75-11(b) of this subpart'' and adding the words ``part 305
of this chapter'' in their place.
Sec. 301.75-11 [Removed and Reserved]
0
9. Section 301.75-11 is removed and reserved.
Sec. 301.81-4 [Amended]
0
10. Section 301.81-4 is amended as follows:
0
a. In paragraph (a)(2)(iii), by removing the words ``the methods and
procedures prescribed in the Appendix to this subpart (``III.
Regulatory Procedures'')'' and adding the words ``part 305 of this
chapter'' in their place.
0
b. In paragraph (b), by removing the words ``the methods and procedures
prescribed in the Appendix to this subpart (``III. Regulatory
Procedures''), or in accordance with the methods and procedures
prescribed in''.
0
11. Section 301.81-5 is amended as follows:
0
a. In paragraph (a)(3)(ii), at the end of the paragraph, by removing
the word ``or''.
0
b. In paragraph (a)(3)(iii), by removing the words ``methods and
procedures prescribed in the Appendix to this subpart (``III.
Regulatory Procedures'').'' and adding the words ``part 305 of this
chapter; or'' in their place.
0
c. By adding a new paragraph (a)(3)(iv) to read as set forth below.
Sec. 301.81-5 Issuance of a certificate or limited permit.
(a) * * *
(3) * * *
(iv) If the article is containerized nursery stock, it has been
produced in accordance with Sec. 301.81-11.
* * * * *
Sec. 301.81-6 [Amended]
0
12. Section 301.81-6 is amended by removing the words ``the ``Imported
Fire Ant Program Manual,'' as set forth in the appendix to this
subpart'' and adding the words ``part 305 of this chapter'' in their
place.
0
13. A new Sec. 301.81-11 is added to read as follows:
Sec. 301.81-11 Imported fire ant detection, control, exclusion, and
enforcement program for nurseries producing containerized plants.
This detection, control, exclusion, and enforcement program is
designed to keep nurseries free of the imported fire ant and provides a
basis to certify containerized nursery stock for interstate movement.
Participating regulated establishments must be operating under a
compliance agreement in accordance with Sec. 301.81-6. Such compliance
agreements shall state the specific requirements that a shipper agrees
to follow to move plants in accordance with the requirements of the
program. Certificates and a nursery identification number may be issued
to the nursery for use on shipments of regulated articles.
(a) Detection. (1) Nursery owners are required to visually survey
their entire premises twice monthly for the presence of imported fire
ants.
(2) Nurseries participating in this program will be inspected by
Federal or State inspectors at least twice per year. More frequent
inspections may be necessary depending upon imported fire ant
infestation levels immediately surrounding the nursery, the
thoroughness of nursery management in maintaining imported-fire-ant-
free premises, and the number of previous detections of imported fire
ants in or near containerized plants. Inspections by Federal and State
inspectors should be more frequent just before and during the peak
shipping season. Any nurseries determined during nursery inspections to
have imported fire ant colonies must be immediately treated to the
extent necessary to eliminate the colonies.
(b) Control. Nursery plants that are shipped under this program
must originate in a nursery that meets the requirements of this
section. Nursery owners must implement a treatment program with
registered bait and contact insecticides. The premises, including
growing and holding areas, must be maintained free of the imported fire
ant. As part of this treatment program, all exposed soil surfaces
(including sod and mulched areas) on property where plants are grown,
potted, stored, handled, loaded, unloaded, or sold must be treated in
accordance with part 305 of this chapter at least once every 6 months.
The first application must be performed early in the spring. Followup
treatments with a contact insecticide in accordance with part 305 of
this chapter must be applied to eliminate all remaining colonies.
(c) Exclusion. (1) For plants grown on the premises, treatment of
soil or potting media in accordance with part 305 of
[[Page 4241]]
this chapter prior to planting is required.
(2) For plants received from outside sources, to prevent the spread
into a nursery free of the imported fire ant by newly introduced,
infested nursery plants, all plants must be:
(i) Obtained from nurseries that comply with the requirements of
this section and that operate under a compliance agreement in
accordance with Sec. 301.81-6; or
(ii) Treated upon delivery in accordance with part 305 of this
chapter, and within the specified number of days be either:
(A) Repotted in treated potting soil media;
(B) Retreated in accordance with part 305 of this chapter at the
specified interval; or
(C) Shipped.
(d) Enforcement. (1) The nursery owner must maintain records of the
nursery's surveys and treatments for the imported fire ant. These
records must be made available to State and Federal inspectors upon
request.
(2) If imported fire ants are detected in nursery stock during an
inspection by a Federal or State inspector, issuance of certificates
for movement will be suspended until necessary treatments are applied
and the plants and nursery premises are determined to be free of the
imported fire ant. A Federal or State inspector may declare a nursery
to be free of the imported fire ant upon reinspection of the premises.
This inspection must be conducted no sooner than 30 days after
treatment. During this period, certification may be based upon
treatments for plants in accordance with part 305 of this chapter.
(3) Upon notification by the department of agriculture in any State
of destination that a confirmed imported fire ant infestation was found
on a shipment from a nursery considered free of the imported fire ant,
the department of agriculture in the State of origin must cease its
certification of shipments from that nursery. An investigation by
Federal or State inspectors will commence immediately to determine the
probable source of the problem and to ensure that the problem is
resolved. If the problem is an infestation, issuance of certification
for movement on the basis of imported-fire-ant-free premises will be
suspended until treatment and elimination of the infestation is
completed. Reinstatement into the program will be granted upon
determination that the nursery premises are free of the imported fire
ant, and that all other provisions of this subpart are being followed.
(4) In cases where the issuance of certificates is suspended
through oral notification, the suspension and the reasons for the
suspension will be confirmed in writing within 20 days of the oral
notification of the suspension. Any person whose issuance of
certificates has been suspended may appeal the decision, in writing,
within 10 days after receiving the written suspension notice. The
appeal must state all of the facts and reasons that the person wants
the Administrator to consider in deciding the appeal. A hearing may be
held to resolve any conflict as to any material fact. Rules of practice
for the hearing will be adopted by the Administrator. As soon as
practicable, the Administrator will grant or deny the appeal, in
writing, stating the reasons for the decision.
Appendix to Subpart--Imported Fire Ant [Removed]
0
14. The Appendix to Subpart--Imported Fire Ant is removed.
Sec. 301.87-5 [Amended]
0
15. In Sec. 301.87-5, paragraph (a)(1)(i) is amended by removing the
words ``Sec. 301.87-10 of this subpart'' and adding the words ``part
305 of this chapter'' in their place.
Sec. 301.87-10 [Removed and Reserved]
0
16. Section 301.87-10 is removed and reserved.
Sec. 301.89-5 [Amended]
0
17. In Sec. 301.89-5, paragraphs (a)(2)(iii) and (b) are amended by
removing the words ``the methods and procedures prescribed in Sec.
301.89-13'' and adding the words ``part 305 of this chapter'' in their
place.
Sec. 301.89-6 [Amended]
0
18. In Sec. 301.89-6, paragraph (a)(3)(iii) is amended by removing the
words ``methods and procedures prescribed in Sec. 301.89-13'' and
adding the words ``part 305 of this chapter'' in their place.
Sec. 301.89-7 [Amended]
0
19. Section 301.89-7 is amended by removing the citation ``Sec.
301.89-13'' and adding the words ``part 305 of this chapter'' in its
place.
Sec. 301.89-12 [Amended]
0
20. In Sec. 301.89-12, paragraphs (a), (b), and (c) are amended by
removing the citation ``Sec. 301.89-13'' and adding the words ``part
305 of this chapter'' in its place.
Sec. 301.89-13 [Removed and Reserved]
0
21. Section 301.89-13 is removed and reserved.
Sec. 301.92-5 [Amended]
0
22. In Sec. 301.92-5, paragraph (a)(1)(i) is amended by removing the
words ``Sec. 301.92-10 or''.
Sec. 301.92-10 [Removed and Reserved]
0
23. Section 301.92-10 is removed and reserved.
0
24. Part 305 is revised to read as follows:
PART 305--PHYTOSANITARY TREATMENTS
Sec.
305.1 Definitions.
305.2 Approved treatments.
305.3 Processes for adding, revising, or removing treatment
schedules.
305.4 Monitoring and certification of treatments.
305.5 Chemical treatment requirements.
305.6 Cold treatment requirements.
305.7 Quick freeze treatment requirements.
305.8 Heat treatment requirements.
305.9 Irradiation treatment requirements.
Authority: 7 U.S.C. 7701-7772 and 7781-7786; 21 U.S.C. 136 and
136a; 7 CFR 2.22, 2.80, and 371.3.
Sec. 305.1 Definitions.
Administrator. The Administrator, Animal and Plant Health
Inspection Service, United States Department of Agriculture, or any
person delegated to act for the Administrator in matters affecting this
part.
APHIS. The Animal and Plant Health Inspection Service, United
States Department of Agriculture.
Cold treatment. Exposure of a commodity to a specified cold
temperature that is sustained for a specific time period to kill
targeted pests, especially fruit flies.
Dose mapping. Measurement of absorbed dose within a process load
using dosimeters placed at specified locations to produce a one-, two-,
or three-dimensional distribution of absorbed dose, thus rendering a
map of absorbed-dose values.
Dosimeter. A device that, when irradiated, exhibits a quantifiable
change in some property of the device that can be related to absorbed
dose in a given material using appropriate analytical instrumentation
and techniques.
Dosimetry system. A system used for determining absorbed dose,
consisting of dosimeters, measurement instruments and their associated
reference standards, and procedures for the system's use.
Fumigant. A gaseous chemical that easily diffuses and disperses in
air and is toxic to the target organism.
Fumigation. Releasing and dispersing a toxic chemical in the air so
that it reaches the target organism in a gaseous state.
[[Page 4242]]
Inspector. Any individual authorized by the Administrator of APHIS
or the Commissioner of Customs and Border Protection, Department of
Homeland Security, to enforce the regulations in this part.
Irradiation. Treatment with any type of ionizing radiation.
Methyl bromide. A colorless, odorless biocide used to fumigate a
wide range of commodities.
Neutralize. To prevent the establishment of a plant pest by killing
it, sterilizing it, preventing its development from an immature stage,
or preventing its emergence from its host.
Plant Protection and Quarantine (PPQ). The Plant Protection and
Quarantine program of APHIS.
PPQ Treatment Manual. The document that contains the treatment
schedules that are approved for use under this part. The Treatment
Manual is available on the Internet at (http://www.aphis.usda.gov/import_export/plants/manuals/index.shtml) or by contacting the Animal
and Plant Health Inspection Service, Plant Protection and Quarantine,
Manuals Unit, 92 Thomas Johnson Drive, Suite 200, Frederick, MD 21702.
Quick freeze. A commercially acceptable method of quick freezing at
subzero temperatures with subsequent storage and transportation at not
higher than 20 [deg]F. Methods that accomplish this are known as quick
freezing, sharp freezing, cold pack, or frozen pack, but may be any
equivalent commercially acceptable freezing method.
Section 18 of Federal Insecticide, Fungicide, and Rodenticide Act
(FIFRA). An emergency exemption granted by the U.S. Environmental
Protection Agency to Federal or State agencies authorizing an
unregistered use of a pesticide for a limited time.
Vacuum fumigation. Fumigation performed in a gas-tight enclosure.
Most air in the enclosure is removed and replaced with a small amount
of fumigant. The reduction in pressure reduces the required duration of
the treatment.
Sec. 305.2 Approved treatments.
(a) Certain commodities or articles require treatment, or are
subject to treatment, prior to interstate movement within the United
States or importation or entry into the United States. Treatment is
required as indicated in parts 301, 318, and 319 of this chapter, on a
permit, or by an inspector.
(b) Approved treatment schedules are set out in the PPQ Treatment
Manual. Treatments may only be administered in accordance with the
treatment requirements of this part and in accordance with treatment
schedules found in the PPQ Treatment Manual.
(c) APHIS is not responsible for losses or damages incurred during
treatment and recommends that a sample be treated first before deciding
whether to treat the entire shipment.
Sec. 305.3 Processes for adding, revising, or removing treatment
schedules.
(a) Normal process for adding, revising, or removing treatment
schedules. Unless there is a need to immediately add, revise, or remove
a treatment schedule, as provided in paragraph (b)(1) of this section,
a treatment schedule may be added to the PPQ Treatment Manual, revised,
or removed from the PPQ Treatment Manual as follows:
(1) Notice of change to treatment schedule. APHIS will publish in
the Federal Register a notice describing the reasons we have determined
that it is necessary to add, revise, or remove a treatment schedule
and, if necessary, making available the new or revised treatment
schedule as it would be added to the PPQ Treatment Manual. In our
notice, we will provide for a public comment period on the new or
revised treatment schedule or on the removal of the treatment schedule
from the PPQ Treatment Manual.
(2) Response to comments. (i) APHIS will issue a notice after the
close of the public comment period indicating that the treatment
schedule specified in the initial notice will be added to the PPQ
Treatment Manual, revised as described in the notice, or removed from
the PPQ Treatment Manual if:
(A) No comments were received on the notice;
(B) The comments on the notice supported our action; or
(C) The comments on the notice were evaluated but did not change
our determination that it is necessary to add, revise, or remove the
treatment schedule, as described in the notice.
(ii) If the notice issued after the close of the public comment
period indicates that a change will be made to the PPQ Treatment
Manual, APHIS will make available a new version of the PPQ Treatment
Manual that reflects the addition, revision, or removal of the
particular treatment schedule.
(iii) If comments present information that causes us to determine
that the change described in the notice is not appropriate, APHIS will
issue a notice informing the public of this determination after the
close of the comment period.
(b) Process for immediately adding, revising, or removing treatment
schedules. Treatment schedules may be immediately added to the PPQ
Treatment Manual, revised, or removed from the PPQ Treatment Manual
under the circumstances described in paragraph (b)(1) of this section
and in accordance with the process described in paragraphs (b)(2) and
(b)(3) of this section.
(1) Circumstances in which the immediate process may be used.
Treatment schedules may be immediately added to the PPQ Treatment
Manual, revised, or removed from the PPQ Treatment Manual if any of the
following circumstances apply:
(i) PPQ has determined that an approved treatment schedule is
ineffective at neutralizing the targeted plant pest(s);
(ii) PPQ has determined that, in order to neutralize the targeted
plant pest(s), the treatment schedule must be administered using a
different process than was previously used;
(iii) PPQ has determined that a new treatment schedule is
effective, based on efficacy data, and that ongoing trade in an article
or articles may be adversely impacted unless the new treatment schedule
is approved for use; or
(iv) The use of a treatment schedule is no longer authorized by the
U.S. Environmental Protection Agency or by any other Federal entity.
(2) Process for immediate change to treatment schedules. If PPQ
determines that one or more of the circumstances in paragraph (b)(1) of
this section applies and that it is necessary to take immediate action,
APHIS will publish in the Federal Register a notice describing the
reasons we have determined that it is necessary to immediately add,
revise, or remove a treatment schedule and, if necessary, making
available the new or revised treatment schedule as it has been added to
the PPQ Treatment Manual. Treatment schedules that have been added to
the PPQ Treatment Manual or revised under this process will be
identified in the PPQ Treatment Manual as having been added or revised
through the immediate process described in this paragraph (b). The PPQ
Treatment Manual will indicate that these treatment schedules are
subject to change or removal based on public comment. In our notice, we
will provide for a public comment period on the new or revised
treatment schedule or on the removal of the treatment schedule from the
PPQ Treatment Manual.
(3) Response to comments. (i) APHIS will issue a notice after the
close of the public comment period affirming the action described in
the initial notice if:
(A) No comments were received on the notice;
[[Page 4243]]
(B) The comments on the notice supported our action; or
(C) The comments on the notice were evaluated but did not change
our determination that it was necessary to add, revise, or remove the
treatment schedule, as described in the notice.
(ii) If the notice issued after the close of the public comment
period indicates that the initial change to the PPQ Treatment Manual is
affirmed, APHIS will make available a new version of the PPQ Treatment
Manual that will reflect the addition, revision, or removal of the
particular treatment schedule in the main body of the PPQ Treatment
Manual.
(iii) If comments present information that causes us to determine
that it is necessary to change a treatment schedule added to the PPQ
Treatment Manual under this process or to further revise a treatment
schedule that was revised under this process, APHIS will publish a
notice in the Federal Register informing the public of this
determination after the close of the comment period and will revise the
treatment schedule accordingly.
(iv) If comments present information that causes us to determine
that the change described in the initial notice was not appropriate,
APHIS will publish a notice in the Federal Register informing the
public of this determination after the close of the comment period and
will, if necessary, remove the new or revised treatment schedule from
the separate section of the PPQ Treatment Manual.
Sec. 305.4 Monitoring and certification of treatments.
(a) All treatments approved under part 305 are subject to
monitoring and verification by APHIS.
(b) Any treatment performed outside the United States must be
monitored and certified by an inspector or an official authorized by
APHIS. During the entire interval between treatment and export, the
consignment must be stored and handled in a manner that prevents any
infestation by pests and noxious weeds.
Sec. 305.5 Chemical treatment requirements.
(a) Certified facility. The fumigation treatment facility must be
certified by APHIS. Facilities are required to be inspected and
recertified annually, or as often as APHIS directs, depending upon
treatments performed, commodities handled, and operations conducted at
the facility. In order to be certified, a fumigation facility must:
(1) Be capable of administering the required dosage range for the
required duration and at the appropriate temperature, as specified in
the treatment schedules in the PPQ Treatment Manual.
(2) Be adequate to contain the fumigant and be constructed from
material that is not reactive to the fumigant.
(3) For vacuum fumigation facilities, be constructed to withstand
required negative pressure.
(b) Monitoring. Treatment must be monitored by an official
authorized by APHIS to ensure proper administration of the treatment,
including that the correct amount of gas reaches the target organism
and that an adequate number and placement of blowers, fans, sampling
tubes, or monitoring lines are used in the treatment enclosure. An
official authorized by APHIS approves, adjusts, or rejects the
treatment.
(c) Treatment procedures. (1) To kill the pest, all chemical
applications must be administered in accordance with an Environmental
Protection Agency (EPA) approved pesticide label and the APHIS-approved
treatment schedule prescribed in the PPQ Treatment Manual. If EPA
cancels approval for the use of a pesticide on a commodity, then the
treatment schedule prescribed in the PPQ Treatment Manual is no longer
authorized for that commodity. If the commodity is not listed on the
pesticide label and/or included in a Federal quarantine or crisis
exemption in accordance with FIFRA section 18, then no chemical
treatment is available.
(2) Temperature/concentration readings must be taken for items
known to be sorptive or whose sorptive properties are unknown when
treatment is administered in chambers at normal atmospheric pressure.
(3) Unless otherwise specified in the PPQ Treatment Manual, the
volume of the commodity stacked inside the treatment enclosure must not
exceed 2/3 of the volume of the enclosure. Stacking must be approved by
an official authorized by APHIS before treatment begins. All
commodities undergoing treatment must be listed on the label or
authorized under Section 18 of FIFRA.
(4) Recording and measuring equipment must be adequate to
accurately monitor the gas concentration, to ensure the correct amount
of gas reaches the pests, and to detect any leaks in the enclosure. At
least three sampling tubes or monitoring lines must be used in the
treatment enclosure.
(5) An adequate number of blowers or fans must be used inside of
the treatment enclosure to uniformly distribute gas throughout the
enclosure. The circulation system must be able to recirculate the
entire volume of gas in the enclosure in 3 minutes or less.
(6) The exposure period begins after all gas has been introduced.
(7) For vacuum fumigation: The vacuum pump must be able to reduce
pressure in the treatment enclosure to 1-2 inches of mercury in 15
minutes or less.
Sec. 305.6 Cold treatment requirements.
(a) Certification of treatment facilities. All facilities or
locations used for refrigerating fruits or vegetables in accordance
with the cold treatment schedules in the PPQ Treatment Manual must be
certified by APHIS. Recertification of the facility or carrier is
required every 3 years, or as often as APHIS directs, depending on
treatments performed, commodities handled, and operations conducted at
the facility. In order to be certified, facilities and carriers must:
(1) Be capable of keeping treated and untreated fruits, vegetables,
or other articles separate so as to prevent reinfestation of articles
and spread of pests;
(2) Have equipment that is adequate to effectively perform cold
treatment.
(b) Places of treatment; ports of entry. Precooling and
refrigeration may be performed prior to, or upon arrival of fruits and
vegetables in the United States, provided treatments are performed in
accordance with applicable requirements of this section. Fruits and
vegetables that are not treated prior to arrival in the United States
must be treated after arrival only in cold storage warehouses approved
by the Administrator and located in the area north of 39[deg] latitude
and east of 104[deg] longitude or at one of the following ports: The
maritime ports of Wilmington, NC; Seattle, WA; Corpus Christi, TX; and
Gulfport, MS; Seattle-Tacoma International Airport, Seattle, WA; and
Hartsfield-Atlanta International Airport, Atlanta, GA.
(c) Cold treatment enclosures. All enclosures, in which cold
treatment is performed, including refrigerated containers, must:
(1) Be capable of maintaining the treatment temperature specified
in the PPQ Treatment Manual before the treatment begins and holding
fruit at or below the treatment temperature during the treatment.
(2) Maintain fruit pulp temperatures according to treatment
schedules with no more than a 0.39 [deg]C (0.7 [deg]F) variation in
temperature between two consecutive hourly readings.
(3) Be structurally sound and adequate to maintain required
temperatures.
[[Page 4244]]
(d) Treatment procedures. (1) All material, labor, and equipment
for cold treatment performed on a vessel must be provided by the vessel
or vessel agent. An official authorized by APHIS monitors, manages, and
advises in order to ensure that the treatment procedures are followed.
(2) Refrigeration must be completed in the container, compartment,
or room in which it is begun.
(3) Fruit that may be cold treated must be safeguarded to prevent
cross-contamination or mixing with other infested fruit.
(4) Fruit intended for in-transit cold treatment must be precooled
to the temperature at which the fruit will be treated prior to
beginning treatment. The in-transit treatment enclosure may not be used
for precooling unless an official authorized by APHIS approves the
loading of the fruit in the treatment enclosure as adequate to allow
for fruit pulp temperatures to be taken prior to beginning treatment.
If the fruit is precooled outside the treatment enclosure, an official
authorized by APHIS will take pulp temperatures manually from a sample
of the fruit as the fruit is loaded for in-transit cold treatment to
verify that precooling was completed. If the pulp temperatures for the
sample are 0.28 [deg]C (0.5 [deg]F) or more above the temperature at
which the fruit will be treated, the pallet from which the sample was
taken will be rejected and returned for additional precooling until the
fruit reaches the treatment temperature. If fruit is precooled in the
treatment enclosure, or if treatment is conducted at a cold treatment
facility in the United States, the fruit must be precooled to the
temperature at which it will be treated, as verified by an official
authorized by APHIS, prior to beginning treatment.
(5) Breaks, damage, etc., in the treatment enclosure that preclude
maintaining correct temperatures must be repaired before the enclosure
is used. An official authorized by APHIS must approve loading of
compartment, number and placement of temperature probes or sensors, and
initial fruit temperature readings before beginning the treatment.
Hanging decks and hatch coamings within vessels may not be used as
enclosures for in-transit cold treatment without prior written approval
from APHIS. Double-stacking of pallets is not allowed.
(6) Only the same type of fruit in the same type of package may be
treated together in a container; no mixture of fruits in containers may
be treated. A numbered seal must be placed on the doors of the loaded
container and may be removed only at the port of destination by an
official authorized by APHIS.
(7) Temperature recording devices used during treatment must be
password-protected and tamperproof. The devices must be able to record
the date, time, and sensor number and automatic and continuous records
of the temperature during all calibrations and during treatment.
Recording devices must be capable of generating temperature charts for
verification by an inspector. If records of calibrations or treatments
are found to have been manipulated, the vessel or container in which
the treatment is performed may be suspended from conducting cold
treatments until proper equipment is installed and an official
authorized by APHIS has recertified it. APHIS' decision to recertify a
vessel or container will take into account the severity of the
infraction that led to suspension.
(8) A minimum of four temperature probes or sensors is required for
vessel holds used as treatment enclosures. A minimum of three
temperature probes or sensors is required for other treatment
enclosures. An official authorized by APHIS will have the option to
require that additional temperature probes or sensors be used,
depending on the size of the treatment enclosure.
(9) Fruit pulp temperatures must be maintained at the temperature
specified in the treatment schedule with no more than a 0.39 [deg]C
(0.7 [deg]F) variation in temperature between two consecutive hourly
readings. Failure to comply with this requirement will result in
invalidation of the treatment unless an official authorized by APHIS
can verify that the pulp temperature was maintained at or below the
treatment temperature for the duration of the treatment.
(10) The time required to complete the treatment begins when all
temperature probes reach the prescribed cold treatment schedule
temperature. Refrigeration continues until the vessel arrives at the
port of destination and the fruit is released for unloading by an
inspector even though this may prolong the period required for the cold
treatment.
(11) Temperatures must be recorded at intervals no longer than 1
hour apart. Gaps of longer than 1 hour will invalidate the treatment or
indicate treatment failure unless an official authorized by APHIS can
verify that the pulp temperature was maintained at or below the
treatment temperature for the duration of the treatment.
(12) Cold treatment is not completed until so declared by an
official authorized by APHIS or the certifying official of the foreign
country; consignments of treated commodities may not be discharged
until APHIS clearance has been fully completed, including review and
approval of treatment record charts.
(13) Cold treatment of fruits in break bulk vessels or containers
must be initiated by an official authorized by APHIS if there is not a
treatment technician who has been trained to initiate cold treatments
for either break bulk vessels or containers.
(14) An official authorized by APHIS may perform audits to ensure
that the treatment procedures comply with the regulations in this
section and that the treatment is administered in accordance with the
treatment schedules in the PPQ Treatment Manual. The official
authorized by APHIS must be given the appropriate materials and access
to the facility, container, or vessel necessary to perform the audits.
(15) An inspector will sample and cut fruit from each consignment
cold treated for Mediterranean fruit fly (Medfly) to monitor treatment
effectiveness. If a single live Medfly in any stage of development is
found, the consignment will be held until an investigation is completed
and appropriate remedial actions have been implemented. If APHIS
determines at any time that the safeguards contained in this section do
not appear to be effective against the Medfly, APHIS may suspend the
importation of fruits from the originating country and conduct an
investigation into the cause of the deficiency.
(16) The cold treatments required for the entry of fruit are
considered necessary for the elimination of plant pests, and no
liability shall attach to the U.S. Department of Agriculture or to any
officer or representative of that Department in the event injury
results to fruit offered for entry in accordance with these
instructions. In prescribing cold treatments of certain fruits, it
should be emphasized that inexactness and carelessness in applying the
treatments may result in injury to the fruit or its rejection for
entry.
(e) Monitoring. Treatment must be monitored by an inspector to
ensure proper administration of the treatment. An inspector must also
approve the recording devices and sensors used to monitor temperatures
and conduct an operational check of the equipment before each use and
ensure sensors are calibrated. An inspector may approve, adjust, or
reject the treatment.
(f) Compliance agreements. Facilities located in the United States
must operate under a compliance agreement
[[Page 4245]]
with APHIS. The compliance agreement must be signed by a representative
of the cold treatment facility and APHIS. The compliance agreement must
contain requirements for equipment, temperature, circulation, and other
operational requirements for performing cold treatment to ensure that
treatments are administered properly. Compliance agreements must allow
officials of APHIS to inspect the facility to monitor compliance with
the regulations.
(g) Workplans. Facilities located outside the United States may
operate in accordance with a bilateral workplan. The workplan, if and
when required, must be signed by a representative of the cold treatment
facility, the national plant protection organization (NPPO) of the
country of origin, and APHIS. The workplans must contain requirements
for equipment, temperature, circulation, and other operational
requirements for performing cold treatment to ensure that cold
treatments are administered properly. Workplans for facilities outside
the United States may also include trust fund agreement information
regarding payment of the salaries and expenses of APHIS employees on
site. Workplans must allow officials of the NPPO and APHIS to inspect
the facility to monitor compliance with APHIS regulations.
(h) Additional requirements for treatments performed after arrival
in the United States.
(1) Maritime port of Wilmington, NC. Consignments of fruit arriving
at the maritime port of Wilmington, NC, for cold treatment, in addition
to meeting all other applicable requirements of this section, must meet
the following special conditions:
(i) Bulk consignments (those consignments which are stowed and
unloaded by the case or bin) of fruit must arrive in fruit fly-proof
packaging that prevents the escape of adult, larval, or pupal fruit
flies.
(ii) Bulk and containerized consignments of fruit must be cold-
treated within the area over which the U.S. Department of Homeland
Security is assigned the authority to accept entries of merchandise, to
collect duties, and to enforce the various provisions of the customs
and navigation laws in force.
(iii) Advance reservations for cold treatment space must be made
prior to the departure of a consignment from its port of origin.
(iv) The cold treatment facility must remain locked during non-
working hours.
(2) Maritime port of Seattle, WA. Consignments of fruit arriving at
the maritime port of Seattle, WA, for cold treatment, in addition to
meeting all other applicable requirements of this section, must meet
the following special conditions:
(i) Bulk consignments (those consignments which are stowed and
unloaded by the case or bin) of fruit must arrive in fruit fly-proof
packaging that prevents the escape of adult, larval, or pupal fruit
flies.
(ii) Bulk and containerized consignments of fruit must be cold
treated within the area over which the U.S. Department of Homeland
Security is assigned the authority to accept entries of merchandise, to
collect duties, and to enforce the various provisions of the customs
and navigation laws in force.
(iii) Advance reservations for cold treatment space must be made
prior to the departure of a consignment from its port of origin.
(iv) The cold treatment facility must remain locked during non-
working hours.
(v) Black light or sticky paper must be used within the cold
treatment facility, and other trapping methods, including APHIS-
approved fruit fly traps, must be used within the 4 square miles
surrounding the cold treatment facility.
(vi) The cold treatment facility must have contingency plans,
approved by the Administrator, for safely destroying or disposing of
fruit.
(3) Airports of Atlanta, GA, and Seattle, WA. Consignments of fruit
arriving at the airports of Atlanta, GA, and Seattle, WA, for cold
treatment, in addition to meeting all other applicable requirements of
this section, must meet the following special conditions:
(i) Bulk and containerized consignments of fruit must arrive in
fruit fly-proof packaging that prevents the escape of adult, larval, or
pupal fruit flies.
(ii) Bulk and containerized consignments of fruit arriving for cold
treatment must be cold treated within the area over which the U.S.
Department of Homeland Security is assigned the authority to accept
entries of merchandise, to collect duties, and to enforce the various
provisions of the customs and navigation laws in force.
(iii) The cold treatment facility and APHIS must agree in advance
on the route by which consignments are allowed to move between the
aircraft on which they arrived at the airport and the cold treatment
facility. The movement of consignments from aircraft to a cold
treatment facility will not be allowed until an acceptable route has
been agreed upon.
(iv) Advance reservations for cold treatment space must be made
prior to the departure of a consignment from its port of origin.
(v) The cold treatment facility must remain locked during non-
working hours.
(vi) Black light or sticky paper must be used within the cold
treatment facility, and other trapping methods, including APHIS-
approved fruit fly traps, must be used within the 4 square miles
surrounding the cold treatment facility.
(vii) The cold treatment facility must have contingency plans,
approved by the Administrator, for safely destroying or disposing of
fruit.
(4) Maritime ports of Gulfport, MS, and Corpus Christi, TX.
Consignments of fruit arriving at the ports of Gulfport, MS, and Corpus
Christi, TX, for cold treatment, in addition to meeting all other
applicable requirements of this section, must meet the following
special conditions:
(i) All fruit entering the port for cold treatment must move in
maritime containers. No bulk consignments (those consignments which are
stowed and unloaded by the case or bin) are permitted.
(ii) Within the container, the fruit intended for cold treatment
must be enclosed in fruit fly-proof packaging that prevents the escape
of adult, larval, or pupal fruit flies.
(iii) All consignments of fruit arriving at the port for cold
treatment must be cold treated within the area over which the U.S.
Department of Homeland Security is assigned the authority to accept
entries of merchandise, to collect duties, and to enforce the various
provisions of the customs and navigation laws in force.
(iv) The cold treatment facility and APHIS must agree in advance on
the route by which consignments are allowed to move between the vessel
on which they arrived at the port and the cold treatment facility. The
movement of consignments from vessel to cold treatment facility will
not be allowed until an acceptable route has been agreed upon.
(v) Advance reservations for cold treatment space at the port must
be made prior to the departure of a consignment from its port of
origin.
(vi) Devanning, the unloading of fruit from containers into the
cold treatment facility, must adhere to the following requirements:
(A) All containers must be unloaded within the cold treatment
facility; and
(B) Untreated fruit may not be exposed to the outdoors under any
circumstances.
[[Page 4246]]
(vii) The cold treatment facility must remain locked during non-
working hours.
(viii) Black lights or sticky paper must be used within the cold
treatment facility, and other trapping methods, including APHIS-
approved fruit fly traps, must be used within the 4 square miles
surrounding the cold treatment facility at the maritime port of
Gulfport, MS, and within the 5 square miles surrounding the cold
treatment facility at the maritime port of Corpus Christi, TX.
(ix) During cold treatment, a backup system must be available to
cold treat the consignments of fruit should the primary system
malfunction. The facility must also have one or more reefers (cold
holding rooms) and methods of identifying lots of treated and untreated
fruits.
(x) The cold treatment facility must have the ability to conduct
methyl bromide fumigations on site.
(xi) The cold treatment facility must have contingency plans,
approved by the Administrator, for safely destroying or disposing of
fruit.
Sec. 305.7 Quick freeze treatment requirements.
Quick freeze treatment for fruits and vegetables imported into the
United States or moved interstate from Hawaii or Puerto Rico must be
conducted in accordance with Sec. Sec. 319.56-12 or 318.13-13,
respectively, of this chapter. The PPQ Treatment Manual indicates the
fruits and vegetables for which quick freeze is an authorized
treatment.
Sec. 305.8 Heat treatment requirements.
(a) Certified facility. The treatment facility must be certified by
APHIS. Recertification is required annually, or as often as APHIS
directs, depending upon treatments performed, commodities handled, and
operations conducted at the facility. In order to be certified, a heat
treatment facility must:
(1) Have equipment that is capable of adequately circulating air or
water (as relevant to the treatment), changing the temperature, and
maintaining the changed temperature sufficient to meet the treatment
schedule parameters in the PPQ Treatment Manual.
(2) Have equipment used to record, monitor, or sense temperature,
maintained in proper working order.
(3) Keep treated and untreated fruits, vegetables, or articles
separate so as to prevent reinfestation and spread of pests.
(b) Monitoring. Treatment must be monitored by an official
authorized by APHIS to ensure proper administration of the treatment.
An official authorized by APHIS approves, adjusts, or rejects the
treatment.
(c) Compliance agreements. Facilities located in the United States
must operate under a compliance agreement with APHIS. The compliance
agreement must be signed by a representative of the heat treatment
facilities located in the United States and APHIS. The compliance
agreement must contain requirements for equipment, temperature, water
quality, circulation, and other measures for performing heat treatments
to ensure that treatments are administered properly. Compliance
agreements must allow officials of APHIS to inspect the facility to
monitor compliance with the regulations.
(d) Workplans. Facilities located outside the United States must
operate in accordance with a workplan. The workplan must be signed by a
representative of the heat treatment facilities located outside the
United States, the national plant protection organization of the
country of origin (NPPO), and APHIS. The workplan must contain
requirements for equipment, temperature, water quality, circulation,
and other measures to ensure that heat treatments are administered
properly. Workplans for facilities outside the United States must
include trust fund agreement information regarding payment of the
salaries and expenses of APHIS employees on site. Workplans must allow
officials of the NPPO and APHIS to inspect the facility to monitor
compliance with APHIS regulations.
(e) Treatment procedures. (1) Before each treatment can begin, an
official authorized by APHIS must approve the loading of the commodity
in the treatment container.
(2) Sensor equipment must be adequate to monitor the treatment, its
type and placement must be approved by an official authorized by APHIS,
and the equipment must be tested by an official authorized by APHIS
prior to beginning the treatment. Sensor equipment must be locked
before each treatment to prevent tampering.
(3) Fruits, vegetables, or articles of substantially different
sizes must be treated separately; oversized fruit may be rejected by an
official authorized by APHIS.
(4) The treatment period begins when the temperature specified by
the treatment schedule has been reached. An official authorized by
APHIS may abort the treatment if the facility requires an unreasonably
long time to achieve the required temperature.
Sec. 305.9 Irradiation treatment requirements.
Irradiation, carried out in accordance with the provisions of this
section, is approved as a treatment for any imported regulated article
(i.e., fruits, vegetables, cut flowers, and foliage); for any regulated
article moved interstate from Hawaii, Puerto Rico, the U.S. Virgin
Islands, Guam, and the Commonwealth of the Northern Marianas Islands
(referred to collectively, in this section, as Hawaii and U.S.
territories); and for any berry, fruit, nut, or vegetable listed as a
regulated article in Sec. 301.32-2(a) of this chapter.
(a) Location of facilities. (1) Where certified irradiation
facilities are available, an approved irradiation treatment may be
conducted for any imported regulated article either prior to shipment
to the United States or in the United States. For any regulated article
moved interstate from Hawaii or U.S. territories, irradiation treatment
may be conducted either prior to movement to the mainland United States
or in the mainland United States. For articles that are imported or
moved interstate from Hawaii or U.S. territories, irradiation
facilities may be located in any State on the mainland United States
except Alabama, Arizona, California, Florida, Kentucky, Louisiana,
Nevada, New Mexico, South Carolina, Tennessee, Texas, and Virginia. In
the States of Georgia, Mississippi, and North Carolina, irradiation
facilities may only be located at the maritime ports of Gulfport, MS,
or Wilmington, NC, or the airport of Atlanta, GA, and only if the
following special conditions are met: The articles to be irradiated
must be imported or moved interstate packaged in accordance with
paragraph (f)(3) of this section; the irradiation facility and APHIS
must agree in advance on the route by which shipments are allowed to
move between the vessel on which they arrive and the irradiation
facility; untreated articles may not be removed from their packaging
prior to treatment under any circumstances; blacklight or sticky paper
must be used within the irradiation facility, and other trapping
methods, including APHIS-approved fruit fly traps, must be used within
the 4 square miles surrounding the facility; and the facility must have
contingency plans, approved by APHIS, for safely destroying or
disposing of regulated articles. Prior to treatment, the fruits and
vegetables to be irradiated may not move into or through any of the
States listed in this paragraph, except that movement is allowed
through Dallas/Fort Worth, TX, as an authorized stop for air cargo, or
as a transloading location for shipments that arrive by air but that
are subsequently transloaded into trucks for overland movement from
[[Page 4247]]
Dallas/Fort Worth into an authorized State by the shortest route.
(2) For articles that are moved interstate from areas quarantined
for fruit flies, irradiation facilities may be located either within or
outside of the quarantined area. If the articles are treated outside
the quarantined area, they must be accompanied to the facility by a
limited permit issued in accordance with Sec. 301.32-5(b) of this
chapter and must be moved in accordance with any safeguards determined
to be appropriate by APHIS.
(b) Approved facilities. The irradiation treatment facility must be
approved by APHIS. In order to be approved, a facility must fulfill the
requirements in paragraphs (c) and (d) of this section.
(c) Compliance agreements. (1) Irradiation facilities treating
imported articles. (i) Compliance agreements with importers and
facility operators for irradiation in the United States. If irradiation
of imported articles is conducted in the United States, both the
importer and the operator of the irradiation facility must sign
compliance agreements with APHIS. In the facility compliance agreement,
the facility operator must agree to comply with any additional
requirements found necessary by APHIS to prevent the escape, prior to
irradiation, of any pests of concern that may be associated with the
articles to be irradiated. In the importer compliance agreement, the
importer must agree to comply with any additional requirements found
necessary by APHIS to ensure the shipment is not diverted to a
destination other than an approved treatment facility and to prevent
escape of plant pests from the articles to be irradiated during their
transit from the port of first arrival to the irradiation facility in
the United States.
(ii) Compliance agreement with irradiation facilities outside the
United States. If irradiation of imported articles is conducted outside
the United States, the operator of the irradiation facility must sign a
compliance agreement with APHIS and the national plant protection
organization (NPPO) of the country in which the facility is located. In
this agreement, the facility operator must agree to comply with the
requirements of this section, and the NPPO of the country in which the
facility is located must agree to monitor that compliance and to inform
the Administrator of any noncompliance.
(2) Irradiation facilities treating articles moved interstate from
Hawaii and U.S. territories. Irradiation facilities treating articles
moved interstate from Hawaii and U.S. territories must complete a
compliance agreement with APHIS as provided in Sec. 318.13-3(d) of
this chapter.
(3) Irradiation facilities treating articles moved interstate from
areas quarantined for fruit flies. Irradiation facilities treating
articles moved interstate from areas quarantined for fruit flies must
complete a compliance agreement with APHIS as provided in Sec. 301.32-
6 of this chapter.
(d) Certified facility. The irradiation treatment facility must be
certified by APHIS. Recertification is required in the event of an
increase in the amount of radioisotope, a decrease in the amount of
radioisotope for a reason other than natural decay, a major
modification to equipment that affects the delivered dose, or a change
in the owner or managing entity of the facility. Recertification also
may be required in cases where a significant variance in dose delivery
has been measured by the dosimetry system. In order to be certified, a
facility must:
(1) Be capable of administering the minimum absorbed ionizing
radiation doses specified in the PPQ Treatment Manual to the regulated
articles;\1\
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\1\ The maximum absorbed ionizing radiation dose and the
irradiation of food is regulated by the Food and Drug Administration
under 21 CFR part 179.
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(2) Be constructed so as to provide physically separate locations
for treated and untreated articles, except that articles traveling by
conveyor directly into the irradiation chamber may pass through an area
that would otherwise be separated. The locations must be separated by a
permanent physical barrier such as a wall or chain link fence 6 or more
feet high to prevent transfer of cartons, or some other means approved
during certification to prevent reinfestation of articles and spread of
pests.
(3) If the facility is to be used to treat imported articles and is
located in the United States, the facility will only be certified if
APHIS determines that regulated articles will be safely transported to
the facility from the port of arrival without significant risk that
plant pests will escape in transit or while the regulated articles are
at the facility.
(e) Monitoring and interagency agreements. Treatment must be
monitored by an inspector. This monitoring will include inspection of
treatment records and unannounced inspections of the facility by an
inspector, and may include inspection of articles prior to or after
irradiation.
(1) Irradiation facilities treating imported articles; irradiation
treatment framework equivalency workplan. The NPPO of a country from
which articles are to be imported into the United States in accordance
with this section must sign a framework equivalency workplan with
APHIS. In this plan, both the NPPO and APHIS will specify the following
items for their respective countries:
(A) Citations for any requirements that apply to the importation of
irradiated fruits and vegetables;
(B) The type and amount of inspection, monitoring, or other
activities that will be required in connection with allowing the
importation of irradiated fruits and vegetables into that country; and
(C) Any other conditions that must be met to allow the importation
of irradiated fruits and vegetables into that country.
(2) Irradiation facilities located in foreign countries. Facilities
in foreign countries that carry out irradiation operations must notify
the Director of Preclearance, PPQ, APHIS, 4700 River Road Unit 140,
Riverdale, MD 20737-1236, of scheduled operations at least 30 days
before operations commence, except where otherwise provided in the
facility preclearance workplan. To ensure the appropriate level of
monitoring, before articles may be imported in accordance with this
section, the following agreements must be signed, in addition to the
irradiation treatment framework equivalency workplan required in
paragraph (e)(1) of this section:
(i) Facility preclearance workplan. Prior to commencing importation
into the United States of articles treated at a foreign irradiation
facility, APHIS and the NPPO of the country from which articles are to
be imported must jointly develop a preclearance workplan that details
the activities that APHIS and the foreign NPPO will carry out in
connection with each irradiation facility to verify the facility's
compliance with the requirements of this section. Typical activities to
be described in this workplan may include frequency of visits to the
facility by APHIS and foreign plant protection inspectors, methods for
reviewing facility records, and methods for verifying that facilities
are in compliance with the requirements for separation of articles,
packaging, labeling, and other requirements of this section. This
facility preclearance workplan will be reviewed and renewed by APHIS
and the foreign NPPO on an annual basis.
(ii) Trust fund agreement. Irradiated articles may be imported into
the United States in accordance with this section only if the NPPO of
the country in which the irradiation facility is located
[[Page 4248]]
or a private export group has entered into a trust fund agreement with
APHIS. That agreement requires the NPPO or the private export group to
pay, in advance of each shipping season, all costs that APHIS estimates
it will incur in providing inspection and treatment monitoring services
at the irradiation facility during that shipping season. Those costs
include administrative expenses and all salaries (including overtime
and the Federal share of employee benefits), travel expenses (including
per diem expenses), and other incidental expenses incurred by APHIS in
performing these services. The agreement will describe the general
nature and scope of APHIS services provided at irradiation facilities
covered by the agreement, such as whether APHIS inspectors will monitor
operations continuously or intermittently, and will generally describe
the extent of inspections APHIS will perform on articles prior to and
after irradiation. The agreement requires the NPPO or private export
group to deposit a certified or cashier's check with APHIS for the
amount of those costs, as estimated by APHIS. If the deposit is not
sufficient to meet all costs incurred by APHIS, the agreement further
requires the NPPO or the private export group to deposit with APHIS a
certified or cashier's check for the amount of the remaining costs, as
determined by APHIS, before any more articles irradiated in that
country may be imported into the United States. After a final audit at
the conclusion of each shipping season, any overpayment of funds would
be returned to the NPPO or the private export group or held on account
until needed, at the option of the NPPO or the private export group.
(3) Irradiation facilities located within the United States.
Facilities located within the United States must notify an inspector at
least 24 hours (excluding Saturday, Sunday, and Federal holidays)
before scheduled operations.\2\ If the facility will be used to treat
imported articles, the NPPO of the country from which the articles are
to be imported into the United States in accordance with this section
must also sign the irradiation treatment framework equivalency workplan
required in paragraph (e)(1) of this section.
---------------------------------------------------------------------------
\2\ Inspectors are assigned to local offices of the Animal and
Plant Health Inspection Service, which are listed in telephone
directories.
---------------------------------------------------------------------------
(f) Packaging. Articles that are irradiated in accordance with this
section must be packaged in cartons in the following manner:
(1) Irradiated articles may not be packaged for shipment in a
carton with nonirradiated articles.
(2) For all imported articles irradiated prior to arrival in the
United States, all articles moved interstate from Hawaii or U.S.
territories and irradiated prior to arrival in the mainland United
States, and all regulated articles to be moved interstate from an area
quarantined for fruit flies that are treated within the quarantined
area:
(i) The fruits and vegetables must be packaged either:
(A) In insect-proof cartons that have no openings that will allow
the entry of the pests of concern. The cartons must be sealed with
seals that will visually indicate if the cartons have been opened. The
cartons may be constructed of any material that prevents entry or
oviposition (if applicable) by the pests of concern into the articles
in the carton;\3\ or
---------------------------------------------------------------------------
\3\ If there is a question as to the adequacy of a carton, send
a request for approval of the carton, together with a sample carton,
to the Animal and Plant Health Inspection Service, Plant Protection
and Quarantine, Center for Plant Health Inspection and Technology,
1730 Varsity Drive, Suite 400, Raleigh, NC 27606-5202.
---------------------------------------------------------------------------
(B) In noninsect-proof cartons that are stored immediately after
irradiation in a room completely enclosed by walls or screening that
completely precludes access by the pests of concern. If stored in
noninsect-proof cartons in a room that precludes access by the pests of
concern, prior to leaving the room, each pallet of cartons must be
completely enclosed in polyethylene shrink wrap, or another solid or
netting covering that completely precludes access to the cartons by the
pests of concern.
(ii) To preserve the integrity of treated lots, each pallet-load of
cartons containing the fruits and vegetables must be secured before
leaving the irradiation facility in one of the following ways:
(A) With polyethylene shrink wrap;
(B) With net wrapping; or
(C) With strapping.
(iii) Packaging must be labeled in a manner that allows an
inspector to determine treatment lot numbers, packing and treatment
facility identification and location, and dates of packing and
treatment.
(A) For imported articles that are treated prior to arrival in the
United States, pallets that remain intact as one unit until entry into
the United States may have one such label per pallet. Pallets that are
broken apart into smaller units prior to or during entry into the
United States, or that will be broken apart into smaller units after
entry into the United States, must have the required label information
on each individual carton.
(B) For articles moved interstate from Hawaii or U.S. territories
that are treated prior to arrival in the mainland United States,
pallets that remain intact as one unit until entry into the mainland
United States may have one such label per pallet. Pallets that are
broken apart into smaller units prior to or during entry into the
mainland United States, or that will be broken apart into smaller units
after entry into the mainland United States, must have the required
label information on each individual carton.
(3) For all articles imported to be irradiated upon arrival in the
United States, moved interstate from Hawaii or U.S. territories to be
irradiated upon arrival in the mainland United States, or moved
interstate from areas quarantined for fruit flies to be irradiated
outside the quarantined area, the articles must be packed in cartons
that have no openings that will allow the exit of the pests of concern
and that are sealed with seals that will visually indicate if the
cartons have been opened. They may be constructed of any material that
prevents the pests of concern from exiting the carton. Cartons of
untreated articles must be shipped in shipping containers sealed prior
to their shipment with seals that will visually indicate if the
shipping containers have been opened.
(g) Containers or vans. Containers or vans that will transport
treated articles must be free of pests of concern prior to loading the
treated articles.
(h) Certification of treatment for articles treated outside the
United States. For each consignment treated in an irradiation facility
outside the United States, a phytosanitary certificate, with the
treatment section completed and issued by the NPPO, must accompany the
consignment.
(i) Dosage. The regulated articles must receive the minimum
absorbed ionizing radiation dose specified in the PPQ Treatment Manual.
(j) Dosimetry systems at the irradiation facility. (1) Dosimetry
must indicate the doses needed to ensure that all the articles will
receive the minimum dose prescribed.
(2) The absorbed dose, as measured using an accurate dosimetry
system, must meet or exceed the absorbed dose for the pest(s) of
concern required by the PPQ Treatment Manual.
(3) When designing the facility's dosimetry system and procedures
for its operation, the facility operator must address guidance and
principles from the International Standards Organization/American
Society for
[[Page 4249]]
Testing and Materials standard\4\ or an equivalent standard recognized
by APHIS.
---------------------------------------------------------------------------
\4\ Designation ISO/ASTM 51261-2002(E), ``Standard Guide for
Selection and Calibration of Dosimetry Systems for Radiation
Processing,'' American Society for Testing and Materials, Annual
Book of ASTM Standards.
---------------------------------------------------------------------------
(k) Records. An irradiation processor must maintain records of each
treated lot for 1 year following the treatment date, and must make
these records available for inspection by an inspector during normal
business hours (8 a.m. to 4:30 p.m., Monday through Friday, except
holidays). These records must include the lot identification, scheduled
process, evidence of compliance with the scheduled process, ionizing
energy source, source calibration, dosimetry, dose distribution in the
product, and the date of irradiation.
(l) Request for initial certification and inspection of facility.
Persons requesting initial certification of an irradiation treatment
facility must submit the request for approval in writing to the Animal
and Plant Health Inspection Service, Plant Protection and Quarantine,
Center for Plant Health Inspection and Technology, 1730 Varsity Drive,
Suite 400, Raleigh, NC 27606-5202. The initial request must identify
the owner, location, and radiation source of the facility, and the
applicant must supply additional information about the facility
construction, treatment protocols, and operations upon request by APHIS
if APHIS requires additional information to evaluate the request.
Before the Administrator determines whether an irradiation facility is
eligible for certification, an inspector will make a personal
inspection of the facility to determine whether it complies with the
standards of this section.
(m) Denial and withdrawal of certification. (1) The Administrator
will withdraw the certification of any irradiation treatment facility
upon written request from the irradiation processor.
(2) The Administrator will deny or withdraw certification of an
irradiation treatment facility when any provision of this section is
not met. Before withdrawing or denying certification, the Administrator
will inform the irradiation processor in writing of the reasons for the
proposed action and provide the irradiation processor with an
opportunity to respond. The Administrator will give the irradiation
processor an opportunity for a hearing regarding any dispute of a
material fact, in accordance with rules of practice that will be
adopted for the proceeding. However, the Administrator will suspend
certification pending final determination in the proceeding if he or
she determines that suspension is necessary to prevent the spread of
any dangerous insect. The suspension will be effective upon oral or
written notification, whichever is earlier, to the irradiation
processor. In the event of oral notification, written confirmation will
be given to the irradiation processor within 10 days of the oral
notification. The suspension will continue in effect pending completion
of the proceeding and any judicial review of the proceeding.
(n) Department not responsible for damage. This treatment is
approved to assure quarantine security against the plant pests listed
in the PPQ Treatment Manual. From the literature available, the
articles authorized for treatment under this section are believed
tolerant to the treatment; however, the facility operator and shipper
are responsible for determination of tolerance. The Department of
Agriculture and its inspectors assume no responsibility for any loss or
damage resulting from any treatment prescribed or monitored.
Additionally, the Nuclear Regulatory Commission is responsible for
ensuring that irradiation facilities are constructed and operated in a
safe manner. Further, the Food and Drug Administration is responsible
for ensuring that irradiated foods are safe and wholesome for human
consumption.
(Approved by the Office of Management and Budget under control numbers
0579-0155, 0579-0215, and 0579-0198)
PART 318--STATE OF HAWAII AND TERRITORIES QUARANTINE NOTICES
0
25. The authority citation for part 318 continues to read as follows:
Authority: 7 U.S.C. 7701-7772 and 7781-7786; 7 CFR 2.22, 2.80,
and 371.3.
Sec. 318.13-3 [Amended]
0
26. In Sec. 318.13-3, paragraph (b)(2) is amended by removing the
words ``approved in'' and adding the words ``approved under'' in their
place.
0
27. Section 318.13-16 is amended as follows:
0
a. In the table in paragraph (a), by adding, under Hawaii, new entries
for litchi and longan in alphabetical order to read as set forth below.
0
b. By adding a new paragraph (b)(1)(ii) to read as set forth below.
Sec. 318.13-16 Regulated articles allowed interstate movement subject
to specified conditions.
(a) * * *
----------------------------------------------------------------------------------------------------------------
State, territory, or Additional
district of origin Common name Botanical name Plant part(s) requirements
----------------------------------------------------------------------------------------------------------------
Hawaii ..................... ..................... ..................... ....................
----------------------------------------------------------------------------------------------------------------
* * * * * * *
----------------------------------------------------------------------------------------------------------------
Litchi Litchi chinensis Fruit (b)(1)(ii),
(b)(3)(ii)
----------------------------------------------------------------------------------------------------------------
Longan Dimocarpus longan Fruit (b)(1)(ii),
(b)(3)(ii)
----------------------------------------------------------------------------------------------------------------
* * * * * * *
----------------------------------------------------------------------------------------------------------------
(b) * * *
(1) * * *
(ii) May not be moved interstate into Florida. Cartons must be
stamped ``Not for movement into or distribution in FL.''
* * * * *
0
28. Section 318.13-22 is amended by revising paragraphs (b)(1) and
(b)(2) to read as follows:
Sec. 318.13-22 Bananas from Hawaii.
* * * * *
(b) * * *
(1) The bananas are irradiated in accordance with part 305 of this
chapter for the Mediterranean fruit fly (Ceratitis capitata), the melon
fruit fly (Bactrocera curcurbitae), the Oriental fruit fly (Bactrocera
dorsalis), and the green scale (Coccus viridis) and are inspected,
[[Page 4250]]
after removal from the stalk, in Hawaii and found to be free of the
banana moth (Opogona sacchari (Bojen)) by an inspector before or after
undergoing irradiation treatment; or
(2) The bananas are irradiated in accordance with part 305 of this
chapter for the Mediterranean fruit fly (Ceratitis capitata), the melon
fruit fly (Bactrocera curcurbitae), and the Oriental fruit fly
(Bactrocera dorsalis) and are inspected, after removal from the stalk,
in Hawaii and found to be free of the green scale (Coccus viridis) and
the banana moth (Opogona sacchari (Bojen)) before or after undergoing
irradiation treatment.
* * * * *
0
29. Section 318.13-25 is revised to read as follows:
Sec. 318.13-25 Sweetpotatoes from Hawaii.
Sweetpotatoes may be moved interstate from Hawaii in accordance
with this section only if the sweetpotatoes meet the conditions in
paragraph (a) or paragraph (b) of this section or if the sweetpotatoes
are fumigated with methyl bromide in accordance with part 305 of this
chapter.
(a) Vapor heat treatment and inspection. (1) The sweetpotatoes must
be treated with vapor heat in accordance with part 305 of this chapter.
(2) The sweetpotatoes must be sampled, cut, and inspected and found
to be free of the ginger weevil (Elytrotreinus subtruncatus). Sampling,
cutting, and inspection must be performed under conditions that will
prevent any pests that may emerge from the sampled sweetpotatoes from
infesting any other sweetpotatoes intended for interstate movement in
accordance with this section.
(3) The sweetpotatoes must be inspected and found to be free of the
gray pineapple mealybug (Dysmicoccus neobrevipes) and the Kona coffee-
root knot nematode (Meloidogyne konaensis).
(4)(i) Sweetpotatoes that are treated in Hawaii must be packaged in
the following manner:
(A) The cartons must have no openings that will allow the entry of
the pests of concern and must be sealed with seals that will visually
indicate if the cartons have been opened. They may be constructed of
any material that prevents the entry of the pests of concern.\5\
---------------------------------------------------------------------------
\5\ If there is a question as to the adequacy of a carton, send
a request for approval of the carton, together with a sample carton,
to the Animal and Plant Health Inspection Service, Plant Protection
and Quarantine, Center for Plant Health Science and Technology, 1730
Varsity Drive, Suite 400, Raleigh, NC 27606.
---------------------------------------------------------------------------
(B) The pallet-load of cartons must be secured before it leaves the
treatment facility in one of the following ways:
(1) With polyethylene sheet wrap;
(2) With net wrapping; or
(3) With strapping.
(C) Packaging must be labeled in a manner that allows an inspector
to determine treatment lot numbers, packing and treatment facility
identification and location, and dates of packing and treatment.
(ii) Cartons of untreated sweetpotatoes that are moving to the
mainland United States for treatment must be shipped in shipping
containers sealed prior to interstate movement with seals that will
visually indicate if the shipping containers have been opened.
(5)(i) Certification on basis of treatment. Certification shall be
issued by an inspector for the movement of sweetpotatoes from Hawaii
that have been treated in accordance with part 305 of this chapter and
handled in Hawaii in accordance with this section.
(ii) Limited permit. A limited permit shall be issued by an
inspector for the interstate movement of untreated sweetpotato from
Hawaii for treatment on the mainland United States in accordance with
this section.
(b) Irradiation treatment and inspection. (1) The sweetpotatoes
must be treated with irradiation in accordance with part 305 of this
chapter.
(2) Sweetpotatoes that are not treated with an irradiation dose
approved to neutralize the ginger weevil (Elytrotreinus subtruncatus)
must be sampled, cut, and inspected and found to be free of the ginger
weevil by an inspector in Hawaii. Sampling, cutting, and inspection
must be performed under conditions that will prevent any pests that may
emerge from the sampled sweetpotatoes from infesting any other
sweetpotatoes intended for interstate movement in accordance with this
section.
(3)(i) To be certified for interstate movement under this
paragraph, sweetpotato from Hawaii must be inspected in Hawaii and
found free of the gray pineapple mealybug (Dysmicoccus neobrevipes) and
the Kona coffee-root knot nematode (Meloidogyne konaensis) by an
inspector before undergoing irradiation treatment in Hawaii.
(ii) To be eligible for a limited permit under this section,
untreated sweetpotato from Hawaii must be inspected in Hawaii and found
free of the gray pineapple mealybug (Dysmicoccus neobrevipes) and the
Kona coffee-root knot nematode (Meloidogyne konaensis) by an inspector.
(Approved by the Office of Management and Budget under control number
0579-0281)
0
30. A new Sec. 318.13-26 is added to read as follows:
Sec. 318.13-26 Breadfruit, jackfruit, fresh pods of cowpea, dragon
fruit, mangosteen, and moringa pods from Hawaii.
(a) Breadfruit and jackfruit. (1) To be eligible for interstate
movement, breadfruit and jackfruit from Hawaii must be treated with
irradiation in accordance with part 305 of this chapter.
(2) To be certified for interstate movement, breadfruit and
jackfruit from Hawaii must be inspected in Hawaii and found free of
spiraling whitefly (Aleurodicus dispersus), inornate scale (Aonidiella
inornata), red wax scale (Ceroplastes rubens), green scale (Coccus
viridis), gray pineapple mealybug (Dysmicoccus neobrevipes), pink
hibiscus mealybug (Maconellicoccus hirsutus), spherical mealybug
(Nipaecoccus viridis), citrus mealybug (Pseudococcus cryptus), melon
thrips (Thrips palmi), and signs of thrip damage before undergoing
irradiation treatment in Hawaii at a dose approved to neutralize fruit
flies. Fruit treated for fruit flies also must either receive a post-
harvest dip in accordance with part 305 of this chapter to treat
external feeders or originate from an orchard or growing area that was
previously treated with a broad-spectrum insecticide during the growing
season and a pre-harvest inspection of the orchard or growing area
found the fruit free of any surface pests as prescribed in a compliance
agreement. Post-treatment inspection in Hawaii is not required if the
fruit undergoes irradiation treatment at a dose approved to neutralize
all plant pests of the class Insecta, except pupae and adults of the
order Lepidoptera. Regardless of irradiation dose, the fruit must be
free of stems and leaves and must originate from an orchard that was
previously treated with a fungicide appropriate for the fungus
Phytophthora tropicalis during the growing season and the fruit must be
inspected prior to harvest and found free of the fungus or, after
irradiation treatment, must receive a post-harvest fungicidal dip
appropriate for Phytophthora tropicalis.
(3) To be eligible for a limited permit, breadfruit and jackfruit
from Hawaii must be free of stems and leaves and must originate from an
orchard that was previously treated with a fungicide appropriate for
the fungus Phytophthora tropicalis during the growing season
[[Page 4251]]
and the fruit must be inspected prior to harvest and found free of the
fungus or, after irradiation treatment, must receive a post-harvest
fungicidal dip appropriate for Phytophthora tropicalis.
(b) Fresh pods of cowpea. (1) To be eligible for interstate
movement, fresh pods of cowpea and its relatives from Hawaii must be
treated with irradiation in accordance with part 305 of this chapter.
(2) To be certified for interstate movement, fresh pods of cowpea
and its relatives from Hawaii must be inspected in Hawaii and found
free of the cassava red mite (Oligonychus biharensis) and adults and
pupae of the order Lepidoptera before undergoing irradiation treatment.
The pods must be free of stems and leaves.
(3) To be eligible for a limited permit, fresh pods of cowpea and
its relatives from Hawaii must be free of stems and leaves and must be
inspected in Hawaii and found free of the cassava red mite (Oligonychus
biharensis) and adults and pupae of the order Lepidoptera.
(c) Dragon fruit. To be certified for interstate movement, dragon
fruit from Hawaii presented for inspection must have the sepals removed
and must be inspected in Hawaii and found free of gray pineapple
mealybug (Dysmicoccus neobrevipes), pink hibiscus mealybug
(Maconellicoccus hirsutus), and citrus mealybug (Pseudococcus cryptus)
before undergoing irradiation treatment in Hawaii at a dose approved to
neutralize fruit flies. Fruit treated for fruit flies also must either
receive a post-harvest dip in accordance with part 305 of this chapter
to treat external feeders or originate from an orchard or growing area
that was previously treated with a broad-spectrum insecticide during
the growing season and a pre-harvest inspection of the orchard or
growing area found the fruit free of any surface pests as prescribed in
a compliance agreement. Post-treatment inspection in Hawaii is not
required if the fruit undergoes irradiation treatment at a dose
approved to neutralize all plant pests of the class Insecta, except
pupae and adults of the order Lepidoptera. Regardless of irradiation
dose, the fruit must be free of stems and leaves.
(d) Mangosteen. To be certified for interstate movement, mangosteen
from Hawaii must have the sepals removed and must be inspected in
Hawaii and found free of gray pineapple mealybug (Dysmicoccus
neobrevipes), pink hibiscus mealybug (Maconellicoccus hirsutus), citrus
mealybug (Pseudococcus cryptus), and Thrips florum before undergoing
irradiation treatment in Hawaii at a dose approved to neutralize fruit
flies. Fruit treated for fruit flies also must either receive a post-
harvest dip in accordance with part 305 of this chapter to treat
external feeders or originate from an orchard or growing area that was
previously treated with a broad-spectrum insecticide during the growing
season and a pre-harvest inspection of the orchard or growing area
found the fruit free of any surface pests as prescribed in a compliance
agreement. Post-treatment inspection in Hawaii is not required if the
fruit undergoes irradiation treatment at a dose approved to neutralize
all plant pests of the class Insecta, except pupae and adults of the
order Lepidoptera. Regardless of irradiation dose, the fruit must be
free of stems and leaves.
(e) Melon. To be certified for interstate movement, melon from
Hawaii must be inspected in Hawaii and found free of spiraling whitefly
(Aleurodicus dispersus) before undergoing irradiation treatment in
Hawaii at a dose approved to neutralize fruit flies. Fruit treated for
fruit flies also must either receive a post-harvest dip in accordance
with part 305 of this chapter to treat external feeders or originate
from an orchard or growing area that was previously treated with a
broad-spectrum insecticide during the growing season and a pre-harvest
inspection of the orchard or growing area found the fruit free of any
surface pests as prescribed in a compliance agreement. Post-treatment
inspection in Hawaii is not required if the fruit undergoes irradiation
treatment at a dose approved to neutralize all plant pests of the class
Insecta, except pupae and adults of the order Lepidoptera. Regardless
of irradiation dose, melons must be washed to remove dirt and must be
free of stems and leaves.
(f) Moringa pods. To be certified for interstate movement, moringa
pods from Hawaii must be inspected in Hawaii and found free of
spiraling whitefly (Aleurodicus dispersus), inornate scale (Aonidiella
inornata), green scale (Coccus viridis), and citrus mealybug
(Pseudococcus cryptus) before undergoing irradiation treatment in
Hawaii at a dose approved to neutralize fruit flies. Fruit treated for
fruit flies also must either receive a post-harvest dip in accordance
with part 305 of this chapter to treat external feeders or originate
from an orchard or growing area that was previously treated with a
broad-spectrum insecticide during the growing season and a pre-harvest
inspection of the orchard or growing area found the fruit free of any
surface pests as prescribed in a compliance agreement. Post-treatment
inspection in Hawaii is not required if the fruit undergoes irradiation
treatment at a dose approved to neutralize all plant pests of the class
Insecta, except pupae and adults of the order Lepidoptera.
Sec. 318.47-3 [Amended]
0
31. In Sec. 318.47-3, paragraph (a) is amended by adding the words
``in accordance with part 305 of this chapter'' after the word
``origin''.
PART 319--FOREIGN QUARANTINE NOTICES
0
32. The authority citation for part 319 continues to read as follows:
Authority: 7 U.S.C. 450, 7701-7772, and 7781-7786; 21 U.S.C. 136
and 136a; 7 CFR 2.22, 2.80, and 371.3.
0
33. In Sec. 319.8-23, paragraph (a)(1) is revised to read as follows:
Sec. 319.8-23 Treatment.
(a)(1) Vacuum fumigation as required in this subpart must be
conducted in accordance with part 305 of this chapter.
* * * * *
Sec. 319.28 [Amended]
0
34. Section 319.28 is amended as follows:
0
a. In paragraph (b)(5), by adding the words ``treated in accordance
with part 305 of this chapter'' after the words ``fumigated with methyl
bromide''; and by removing the second sentence.
0
b. In paragraphs (b)(7)(i) and (b)(7)(ii), by removing the words
``paragraph (b)(5) of this section'' and adding the words ``part 305 of
this chapter'' in their place.
Sec. 319.37-13 [Amended]
0
35. In Sec. 319.37-13, paragraph (c) is amended by removing the words
``the Plant Protection and Quarantine Treatment Manual'' and adding the
words ``7 CFR part 305'' in their place.
0
36. In Sec. 319.40-3, paragraph (b)(1) is revised to read as follows:
Sec. 319.40-3 General permits; articles that may be imported without
a specific permit; articles that may be imported without either a
specific permit or an importer document.
* * * * *
(b) * * *
(1) The wood packaging material must have been treated in
accordance with part 305 of this chapter.
* * * * *
0
37. Section 319.40-5 is amended as follows:
0
a. In paragraph (b)(1)(i)(C), by removing the citation ``Sec. 319.40-
7(f)(1)'' and adding the words ``part 305 of this chapter'' in its
place.
0
b. In paragraph (b)(1)(i)(D), by removing the citation ``Sec. 319.40-
7(d)''
[[Page 4252]]
and adding the words ``part 305 of this chapter'' in its place.
0
c. In paragraph (b)(1)(iii)(A), by removing the citations ``Sec.
319.40-7(c)'' and ``Sec. 319.40-7(d)'' and adding the words ``part 305
of this chapter'' in their place.
0
d. In paragraph (b)(1)(iii)(C), by removing the citations ``Sec.
319.40-7(c)'', ``Sec. 319.40-7(d)'', and ``Sec. 319.40-7(f)(3)'' each
time they occur and adding the words ``part 305 of this chapter'' in
their place.
0
e. In paragraph (b)(2)(i), by removing the citation ``Sec. 319.40-
7(f)(2)'' and adding the words ``part 305 of this chapter'' in its
place.
0
f. In paragraph (b)(2)(ii), by removing the citations ``Sec. 319.40-
7(c)'' and ``Sec. 319.40-7(d)'' and adding the words ``part 305 of
this chapter'' in their place.
0
g. In paragraph (c)(2), by removing the citation ``Sec. 319.40-
7(f)(1)'' and adding the words ``part 305 of this chapter'' in its
place.
0
h. In paragraph (d), by removing the citation ``Sec. 319.40-7(f)'' and
adding the words ``part 305 of this chapter'' in its place.
0
i. In paragraph (f), by removing the citation ``Sec. 319.40-7(c)'' and
adding the words ``part 305 of this chapter'' in its place.
0
j. By revising paragraph (l)(3) to read as set forth below.
0
k. In paragraph (m)(2)(iv)(A)(1), by removing the citation ``319.40-
7(f)'' and adding the words ``part 305'' in its place.
0
l. In paragraph (m)(2)(iv)(A)(4), by removing the citation ``Sec.
319.40-6'' and adding the words ``7 CFR part 305'' in its place.
0
m. In paragraph (n)(1)(ii), by removing the citation ``Sec. 319.40-
7(c)'' and adding the words ``part 305 of this chapter'' in its place.
Sec. 319.40-5 Importation and entry requirements for specific
articles.
* * * * *
(l) * * *
(3) Are fumigated in accordance with part 305 of this chapter prior
to arrival in the United States.
* * * * *
Sec. 319.40-6 [Amended]
0
38. Section 319.40-6 is amended as follows:
0
a. In paragraph (a), by removing the citation ``Sec. 319.40-7(c)'' and
adding the words ``part 305 of this chapter'' in their place.
0
b. In paragraphs (b)(1) introductory text, (b)(1)(i), (b)(1)(ii),
(b)(2)(ii), (c)(2)(i)(B), (c)(2)(iii), (c)(2)(iv), and (d), by removing
the citation ``Sec. 319.40-7(c)'' each time it occurs and adding the
words ``part 305 of this chapter'' in its place; and by removing the
citation ``Sec. 319.40-7(d)'' each time it occurs and adding the words
``part 305 of this chapter'' in its place.
0
c. In paragraph (c)(1)(i)(A), by removing the citation ``Sec. 319.40-
7(e)'' each time it occurs and adding the words ``part 305 of this
chapter'' in its place.
0
d. In paragraphs (c)(2)(i)(B), (c)(2)(iii), (c)(2)(iv), and (d), by
removing the citation ``Sec. 319.40-7(f)(3)'' each time it occurs and
adding the words ``part 305 of this chapter'' in its place.
0
39. Section 319.40-7 is amended as follows:
0
a. By removing paragraphs (c) through (f).
0
b. By adding a new paragraph (c) to read as set forth below.
0
c. By redesignating paragraph (g) as paragraph (d).
Sec. 319.40-7 Treatments and safeguards.
* * * * *
(c) Treatments. Treatment of regulated articles under this subpart
must be conducted in accordance with part 305 of this chapter.
* * * * *
Sec. 319.41-5 [Amended]
0
40. Section 319.41-5 is amended as follows:
0
a. In paragraph (a), second sentence, by removing the words ``other
necessary''; and by adding the words ``in accordance with part 305 of
this chapter,'' after the word ``treatment''.
0
b. In paragraph (a), third sentence, by adding the words ``in
accordance with part 305 of this chapter'' after the word
``treatment''.
0
c. In paragraphs (b), (c), (d)(1), and (d)(3), by adding the words ``in
accordance with part 305 of this chapter'' after the words ``other
treatment'' each time they occur.
Sec. 319.41-5a [Removed]
0
41. Section 319.41-5a is removed.
Sec. 319.55-6 [Amended]
0
42. Section 319.55-6 is amended as follows:
0
a. In paragraph (a), in the first sentence, by adding the words ``in
accordance with part 305 of this chapter'' after the word
``disinfection''; and in the second sentence, by adding the words ``in
accordance with part 305 of this chapter'' after the word
``treatment''.
0
b. In paragraph (b)(1), in the first sentence, by adding the words ``in
accordance with part 305 of this chapter'' after the word
``treatment.''
Sec. 319.56-3 [Amended]
0
43. In Sec. 319.56-3, paragraph (c)(2) is amended by removing the
citation ``Sec. 305.15'' and adding the words ``part 305'' in its
place.
Sec. 319.56-7 [Amended]
0
44. In Sec. 319.56-7, paragraph (b)(1)(ii) is amended by removing the
words ``with an approved treatment listed in'' and adding the words
``in accordance with'' in their place.
Sec. 319.56-11 [Amended]
0
45. In Sec. 319.56-11, paragraph (b)(1) is amended by removing the
words ``with an approved treatment listed in'' and adding the words
``in accordance with'' in their place.
Sec. 319.56-12 [Amended]
0
46. Section 319.56-12 is amended by removing in the second sentence the
words ``at a temperature not higher than 20 [deg]F during shipping and
upon arrival in the United States, and''; and by removing the third
sentence.
Sec. 319.56-13 [Amended]
0
47. Section 319.56-13 is amended as follows:
0
a. In paragraph (b)(1)(ii), by removing the words ``an approved
treatment listed in''.
0
b. In paragraphs (b)(5)(xiii) and (b)(5)(xv), by removing the words
``with an approved treatment listed in 7 CFR'' and adding the words
``in accordance with'' in their place; and by adding the words ``of
this chapter'' after the words ``part 305''.
Sec. 319.56-21 [Amended]
0
48. In Sec. 319.56-21, paragraphs (b)(2) and (d)(2) are amended by
removing the words ``an approved treatment listed in''.
0
49. In Sec. 319.56-22, paragraph (g)(2) is revised to read as follows:
Sec. 319.56-22 Apples and pears from certain countries in Europe.
* * * * *
(g) * * *
(2) Treatments must be conducted in accordance with part 305 of
this chapter.
* * * * *
0
50. Section 319.56-23 is amended as follows:
0
a. In footnote 3, by removing the words ``a treatment listed in''.
0
b. By revising paragraph (f)(2) to read as set forth below.
Sec. 319.56-23 Apricots, nectarines, peaches, plumcot, and plums from
Chile.
* * * * *
(f) * * *
[[Page 4253]]
(2) Treatments must be conducted in accordance with part 305 of
this chapter.
* * * * *
Sec. 319.56-38 [Amended]
0
51. In Sec. 319.56-38, paragraph (d)(4)(ii)(B) is amended by removing
the words ``an authorized treatment for the pest is available in'' and
adding the words ``a treatment for the pest is authorized by'' in their
place.
Sec. 319.56-46 [Amended]
0
52. In Sec. 319.56-46, paragraph (a) is amended by removing the words
``by receiving a minimum absorbed dose of 400 Gy'' and adding the words
``for plant pests of the class Insecta, except pupae and adults of the
order Lepidoptera'' in their place; and by removing the citation
``Sec. 305.31'' and adding the words ``part 305'' in its place.
Sec. 319.56-47 [Amended]
0
53. Section 319.56-47 is amended as follows:
0
a. In paragraph (b), by removing the citation ``Sec. 305.31'' and
adding the words ``part 305'' in its place.
0
b. In paragraph (d), by removing the citation ``Sec. 305.31'' and
adding the words ``part 305 of this chapter'' in its place.
0
54. In Sec. 319.59-4, paragraph (d)(3) is revised to read as follows:
Sec. 319.59-4 Karnal bunt.
* * * * *
(d) * * *
(3) Items that require disinfection prior to entry into the United
States must be disinfected in accordance with part 305 of this chapter.
* * * * *
0
55. Section 319.74-2 is amended as follows:
0
a. By redesignating the introductory text to paragraph (c)(1) as the
introductory text to paragraph (c); removing paragraph (c)(2); and
redesignating paragraphs (c)(1)(i) and (c)(1)(ii) as paragraphs (c)(1)
and (c)(2), respectively.
0
b. In the newly redesignated introductory text of paragraph (c), by
removing the words ``paragraph (c)(2) of this section'' and adding the
words ``part 305 of this chapter'' in their place.
0
c. By revising the first two sentences of paragraph (e) to read as set
forth below.
Sec. 319.74-2 Conditions governing the entry of cut flowers.
* * * * *
(e) Irradiation. Cut flowers and foliage that are required under
this part to be treated or subjected to inspection to control one or
more of the plant pests for which irradiation is an approved treatment
under part 305 of this chapter may instead be treated with irradiation.
Irradiation treatment must be conducted in accordance with the
requirements of part 305 of this chapter. * * *
* * * * *
PART 330--FEDERAL PLANT PEST REGULATIONS; GENERAL; PLANT PESTS;
SOIL, STONE, AND QUARRY PRODUCTS; GARBAGE
0
56. The authority citation for part 330 continues to read as follows:
Authority: 7 U.S.C. 450, 7701-7772, 7781-7786, and 8301-8317; 21
U.S.C. 136 and 136a; 31 U.S.C. 9701; 7 CFR 2.22, 2.80, and 371.3.
Sec. 330.106 [Amended]
0
57. In Sec. 330.106, paragraph (a) is amended by adding in the fourth
sentence the words ``in accordance with part 305 of this chapter''
after the word ``treatment.''
Sec. 330.300 [Amended]
0
58. In Sec. 330.300, paragraph (a) is amended by removing the words
``methods of'' and by adding the words ``in accordance with part 305 of
this chapter'' after the word ``treatment.''
PART 352--PLANT QUARANTINE SAFEGUARD REGULATIONS
0
59. The authority citation for part 352 continues to read as follows:
Authority: 7 U.S.C. 7701-7772 and 7781-7786; 21 U.S.C. 136 and
136a; 31 U.S.C. 9701; 7 CFR 2.22, 2.80, and 371.3.
Sec. 352.10 [Amended]
0
60. In Sec. 352.10, paragraph (b)(2)(viii) is amended by adding the
words ``in accordance with part 305 of this chapter'' after the word
``treatment.''
Sec. 352.30 [Amended]
0
61. In Sec. 352.30, paragraph (a)(4)(iii) is amended by removing the
word ``such'' and by adding the word ``any'' in its place; and by
adding the words ``in accordance with part 305 of this chapter'' after
the word ``treatment.''
Done in Washington, DC, January 19, 2010.
Kevin Shea
Acting Administrator, Animal and Plant Health Inspection Service.
[FR Doc. 2010-1375 Filed 1-25-10: 8:45 am]
BILLING CODE 3410-34-S