[Federal Register: May 12, 2009 (Volume 74, Number 90)]
[Proposed Rules]
[Page 22317-22345]
From the Federal Register Online via GPO Access [wais.access.gpo.gov]
[DOCID:fr12my09-23]
[[Page 22317]]
-----------------------------------------------------------------------
Part III
Department of Agriculture
-----------------------------------------------------------------------
Animal and Plant Health Inspection Service
-----------------------------------------------------------------------
7 CFR Parts 301, 305, 318, et al.
Phytosanitary Treatments; Location of and Process for Updating
Treatment Schedules; Proposed Rule
[[Page 22318]]
-----------------------------------------------------------------------
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: Proposed rule.
-----------------------------------------------------------------------
SUMMARY: We are proposing to revise 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 would remove treatment
schedules from other places where they are currently found in 7 CFR
chapter III as well. Approved treatment schedules would instead be
found in the Plant Protection and Quarantine Treatment Manual, which is
available on the Internet. We are also proposing to establish a new
process to provide the public with notice and the opportunity to
comment on changes to treatment schedules. Finally, we would 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. These changes would simplify and expedite our processes
for adding, changing, and removing treatment schedules while continuing
to provide for public participation in the process. These changes would
also simplify our presentation of treatments to the public by
consolidating all treatments into one document and eliminating
redundant text from the regulations.
DATES: We will consider all comments that we receive on or before July
13, 2009.
ADDRESSES: You may submit comments by either of the following methods:
Federal eRulemaking Portal: Go to http://
www.regulations.gov/fdmspublic/ component/
main?main=DocketDetail&d=APHIS-2008-0022 to submit or view comments and
to view supporting and related materials available electronically.
Postal Mail/Commercial Delivery: Please send two copies of
your comment to Docket No. APHIS-2008-0022, Regulatory Analysis and
Development, PPD, APHIS, Station 3A-03.8, 4700 River Road Unit 118,
Riverdale, MD 20737-1238. Please state that your comment refers to
Docket No. APHIS-2008-0022.
Reading Room: You may read any comments that we receive on this
docket in our reading room. The reading room is located in room 1141 of
the USDA South Building, 14th Street and Independence Avenue, SW.,
Washington, DC. Normal reading room hours are 8 a.m. to 4:30 p.m.,
Monday through Friday, except holidays. To be sure someone is there to
help you, please call (202) 690-2817 before coming.
Other Information: Additional information about APHIS and its
programs is available on the Internet at http://www.aphis.usda.gov.
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) 734-8758.
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.
Broadly speaking, the regulations in part 305 contain four types of
provisions:
General requirements to follow approved treatment
schedules and provisions for monitoring and certifying treatments.
Lists of approved treatments for fruits, vegetables, and
other articles. These are currently contained in Sec. 305.2. Entries
in the lists of approved treatments include the article in question,
the pests of concern, and the treatment approved to neutralize those
pests for that article. For fruits and vegetables, whose approved
treatments are listed in paragraph (h) of Sec. 305.2, entries in the
lists also include the country or area of origin of the fruit or
vegetable for which treatment is approved.
General requirements for each type of treatment (chemical
treatment, heat treatment, cold treatment, etc.). These include
requirements for treatment facility construction, certifying or
approving treatment facilities, and performing and monitoring
treatments. These requirements are contained at the beginning of
treatment-specific subparts. For example, ``Subpart--Chemical
Treatments'' begins with a section (Sec. 305.5) that sets out
requirements for facilities performing chemical treatments, general
chemical treatment procedures, and requirements for monitoring chemical
treatments.
Treatment schedules. For example, in ``Subpart--Chemical
Treatments,'' Sec. 305.6 contains various methyl bromide fumigation
treatment schedules, which set out the required pressure, temperature,
dosage rate, and exposure period for each schedule. Some treatment
schedules are also found elsewhere in 7 CFR chapter III. For example,
some treatment schedules for logs, lumber, and other unmanufactured
wood articles are contained in Sec. 319.40-7.
Most of the phytosanitary treatments authorized by the Animal and
Plant Health Inspection Service (APHIS) and listed in part 305 are also
contained in the Plant Protection and Quarantine (PPQ) Treatment
Manual. Among other things, the PPQ Treatment Manual contains
approximately 400 treatment schedules, detailed instructions for
administering the treatments, and requirements for certification of
facilities that administer the treatments. The PPQ Treatment Manual may
be found on the Internet at http://www.aphis.usda.gov/import_export/
plants/manuals/ports/treatment.shtml.
We are proposing to remove the lists of authorized treatments and
treatment schedules from the regulations, while retaining the general
requirements for performing treatments and certifying or approving
treatment facilities. We would remove treatment schedules from other
places where they are currently found in parts 301 and 319 as well.
Treatment schedules in those parts that are not currently found in the
PPQ Treatment Manual would be added to it, and the PPQ Treatment Manual
would serve as the official reference for all approved treatment
schedules. The inclusion of a treatment schedule in the PPQ Treatment
Manual would indicate that the treatment was approved, making the
inclusion of separate lists of approved treatments in the regulations
unnecessary.
[[Page 22319]]
The general requirements to follow approved treatment schedules and
the specific provisions for monitoring and certification would be
retained in the regulations. The regulations would refer the reader to
the PPQ Treatment Manual as the source for approved treatment
schedules. We would also retain the general requirements for each type
of treatment in part 305.
We are also proposing to establish a new process to make changes to
the lists of approved treatments and the treatment schedules that would
be contained in the Treatment Manual. Rather than making changes
through the rulemaking process, as is necessary for treatments listed
in the regulations, we would publish notices in the Federal Register to
inform the public of the change we are proposing and to solicit
comments. Following the close of the comment period, we would also
publish notices to inform the public of our decision.
The regulations in Sec. 319.56-4(c)(2) set out a process by which
APHIS can authorize the importation of fruits and vegetables through
the publication of notices in the Federal Register. This process can be
used if a pest risk analysis is completed and APHIS makes the
determination that the application of one or more of the designated
phytosanitary measures listed in paragraph (b) of Sec. 319.56-4 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. One of the measures listed in paragraph
(b) is treatment in accordance with part 305. Imports are authorized
through this process by announcing, through the publication of a notice
in the Federal Register, the availability of the pest risk analysis and
the Administrator's determination that the application of one or more
of the designated measures is sufficient to address the risk. A
subsequent notice may then be issued to announce our intent to issue a
permit to authorize importation of the commodity.
However, the current structure of part 305 often makes it
impossible to use the notice-based process for authorizing the
importation of fruits and vegetables in Sec. 319.56-4 if one of the
designated measures to address pest risk is a phytosanitary treatment.
As noted earlier, in the lists of authorized treatments for imported
fruits and vegetables in Sec. 305.2(h)(2)(i), fruits and vegetables
are listed by their country of origin. This is inappropriate because
the country of origin of a fruit or vegetable does not necessarily
affect the efficacy of a treatment at neutralizing the pest associated
with that fruit or vegetable. For example, we would expect the cold
treatment schedule CT T107-a to be effective at neutralizing the
Mediterranean fruit fly (Ceratitis capitata) in grapes from any
country, and it is currently listed as an approved treatment for that
pest for grapes from several countries. The PPQ Treatment Manual
recognizes this principle; it does not typically include countries in
its lists of commodities, pests, and approved treatments.\1\ As part of
this proposed action, we would also remove any specific country
designations on treatments in the PPQ Treatment Manual, except when
country-specific circumstances or lack of data on a treatment's
efficacy have led us to approve a treatment only for a specific
country-commodity-pest combination.
---------------------------------------------------------------------------
\1\ PPQ maintains a separate database, the Fruits and Vegetables
Import Requirements database, that provides information about
countries from which the importation of fruits and vegetables is
approved and, among other things, any treatments that may be
required. This database is available at http://www.aphis.usda.gov/
import_export/plants/plant_imports/quarantine_56/favir.shtml.
---------------------------------------------------------------------------
Currently, to approve the use of a treatment for a fruit or
vegetable from a new country that is affected by a pest for which there
is an approved treatment, we must amend the regulations in part 305. To
authorize the importation of grapes from a new country subject to
treatment with CT T107-a for Mediterranean fruit fly, we would need to
undertake rulemaking to add the new country to the list in Sec.
305.2(h)(2)(i) as a country from which grapes may be treated with CT
T107-a, even though we could otherwise authorize the importation of
those grapes through the notice-based process in Sec. 319.56-4.
Similarly, countries requesting that we allow the importation of a
commodity sometimes provide efficacy data on treatments for pests
prevalent in that country. Reviewing this information often allows us
to develop a treatment schedule to neutralize those pests. For example,
Australia could submit data on the efficacy of cold treatment for fruit
flies in strawberries, a commodity for which we currently have no
approved treatment schedules, as part of a request that we approve the
importation of strawberries from Australia. If treatment was one of the
phytosanitary measures we determined to be necessary to mitigate the
risk associated with strawberries from Australia, strawberries from
Australia would not be eligible for the notice-based process in Sec.
319.56-4 until the new treatment schedule was added through rulemaking.
We currently have no means to add a new approved treatment schedule
except through the rulemaking process.
In both of the cases described above, establishing a notice-based
process to amend the lists of approved treatments and treatment
schedules would enable additional use of the streamlined process in
Sec. 319.56-4 to authorize the importation of fruits and vegetables.
As APHIS pursues the use of streamlined processes for approving the
movement of other commodities in the future, we expect that we would
need to approve new treatments.
In this proposal, we would also establish a process by which we
could make immediate changes to the lists of approved treatments and to
the treatment schedules, also through publishing notices in the Federal
Register. We would only use the process for making immediate changes in
certain circumstances, which would be listed in the regulations.
When we discover pests that have not been neutralized after an
article has been treated for those pests, we may make immediate changes
to the relevant treatment schedule to ensure its continued
effectiveness (unless we determine that the treatment has not been
correctly applied, in which case we take other actions). We may also
need to remove a treatment schedule if it cannot be adjusted to make it
effective, and in some cases we may need to add a new one in its place
to allow trade in a commodity to continue. In addition, treatment
schedules developed for certain conditions may become difficult to
administer if those circumstances change; there may be a simple
adjustment that can be made to the treatment schedule that will ensure
that it can still be administered, without affecting its efficacy.
Finally, the use of certain treatments, particularly chemical
treatments, is dependent on the authorization of other Federal
agencies, and we may need to withdraw certain treatment schedules
immediately if those treatments are no longer authorized.
The Plant Protection Act (7 U.S.C. 7701 et seq.) provides APHIS
with the necessary statutory authority to take some of these actions
immediately, and we will do so whenever necessary to ensure that
treatments are effective at neutralizing plant pests. In addition, we
would not allow treatments to be performed if another Federal agency
does not permit them to be performed; the chemical treatment
regulations in current Sec. 305.5(c)(1) make this clear by stating
that if the U.S. Environmental Protection Agency (EPA) cancels approval
for the use of a pesticide on a commodity, then the treatment schedule
[[Page 22320]]
prescribed in the PPQ Treatment Manual is no longer authorized for that
commodity. Having a notice-based process in place for making immediate
changes to the lists of approved treatments or to the treatment
schedules would ensure that the PPQ Treatment Manual contains only
approved treatment schedules, ensure that our decisionmaking processes
are transparent, and give the public an opportunity to provide input on
changes to the PPQ Treatment Manual.
In addition to approved treatment schedules, the PPQ Treatment
Manual contains other information, such as the procedures for
performing certain types of treatments (e.g., fumigation under a
tarpaulin). Under this proposal, only the approved treatment schedules
in the PPQ Treatment Manual, including information such as the
temperature, duration, dose, or end point of the treatment, would need
to be amended using the notice-based process described in this
proposal. Other information in the PPQ Treatment Manual, such as the
detailed information on treatment preparation, administering
treatments, facility construction, and compliance with other applicable
Federal regulations, would be amended without requesting comment from
the public, as is the case now.
Changes to 7 CFR Part 305
Much of part 305 would be removed under this proposal. We are
providing a distribution table and a derivation table below to give the
reader an overview of the changes we are proposing. Those changes are
discussed in detail directly after the tables.
Table 1--Distribution of Current 7 CFR Part 305
----------------------------------------------------------------------------------------------------------------
Current section Section title (subject) New location Comments
----------------------------------------------------------------------------------------------------------------
305.1....................... Definitions............... 305.1..................... Changes made to section to
reflect removal of
schedules, references to
PPQ Treatment Manual.
305.2....................... Approved treatments....... Paragraph (a) remains in Some changes.
305.2; rest added to PPQ
Treatment Manual.
305.3....................... Monitoring and 305.4..................... Some changes.
certification of
treatments.
305.5....................... Treatment requirements 305.5..................... Updates to refer to PPQ
(chemical treatments). Treatment Manual.
305.6....................... Methyl bromide fumigation PPQ Treatment Manual......
treatment schedules.
305.7....................... Phosphine treatment PPQ Treatment Manual......
schedules.
305.8....................... Sulfuryl fluoride PPQ Treatment Manual......
treatment schedules.
305.9....................... Aerosol spray for aircraft PPQ Treatment Manual......
treatment schedules.
305.10...................... Treatment schedules for PPQ Treatment Manual......
combination treatments.
305.11...................... Miscellaneous chemical PPQ Treatment Manual......
treatments.
305.15...................... Treatment requirements 305.6..................... Updates to refer to PPQ
(cold treatment). Treatment Manual.
305.16...................... Cold treatment schedules.. PPQ Treatment Manual......
305.17...................... Authorized treatments; 305.7..................... No longer lists approved
exceptions (quick freeze). treatments.
305.18...................... Quick freeze treatment PPQ Treatment Manual......
schedule.
305.20...................... Treatment requirements 305.8..................... Updates to refer to PPQ
(heat treatment). Treatment Manual.
305.21...................... Hot water dip treatment PPQ Treatment Manual......
schedule for mangoes.
305.22...................... Hot water immersion PPQ Treatment Manual......
treatment schedules.
305.23...................... Steam sterilization PPQ Treatment Manual......
treatment schedules.
305.24...................... Vapor heat treatment PPQ Treatment Manual......
schedules.
305.25...................... Dry heat treatment PPQ Treatment Manual......
schedules.
305.26...................... Khapra beetle treatment PPQ Treatment Manual......
schedule for feeds and
milled products.
305.27...................... Forced hot air treatment PPQ Treatment Manual......
schedules.
305.28...................... Kiln sterilization PPQ Treatment Manual......
treatment schedule.
305.29...................... Vacuum heat treatment PPQ Treatment Manual......
schedule.
305.31...................... Irradiation treatment of 305.9. Sec. Sec. 305.31,
imported regulated 305.32, and 305.34 would
articles for certain be combined and
plant pests. harmonized.
305.32...................... Irradiation treatment of 305.9.....................
regulated articles to be
moved interstate from
areas quarantined for
fruit fly.
305.34...................... Irradiation treatment of 305.9.....................
certain regulated
articles from Hawaii,
Puerto Rico, and the U.S.
Virgin Islands.
305.40...................... Garbage treatment PPQ Treatment Manual......
schedules for insect
pests and pathogens.
305.42...................... Miscellaneous treatment PPQ Treatment Manual......
schedules.
----------------------------------------------------------------------------------------------------------------
[[Page 22321]]
Table 2--Derivation of Proposed 7 CFR Part 305
----------------------------------------------------------------------------------------------------------------
Section Title Derivation
----------------------------------------------------------------------------------------------------------------
305.1.................. Definitions................................ Current Sec. 305.1.
305.2.................. Approved treatments........................ Current Sec. 305.2(a).
305.3.................. Process for adding, revising, or removing New language.
treatment schedules.
305.4.................. Monitoring and certification of treatments. Current Sec. 305.3.
305.5.................. Chemical treatment requirements............ Current Sec. 305.5.
305.6.................. Cold treatment requirements................ Current Sec. 305.15.
305.7.................. Quick freeze treatment requirements........ Current Sec. 305.17.
305.8.................. Heat treatment requirements................ Current Sec. 305.20.
305.9.................. Irradiation treatment requirements......... Current Sec. Sec. 305.31, 305.32, and
305.34.
----------------------------------------------------------------------------------------------------------------
Definitions (Sec. 305.1)
We would remove the definitions of the following terms, as these
terms are only referred to in the treatment schedules in 7 CFR part
305: autoclaving, forced hot air, hitchhiker pest, hot water immersion
dip, phosphine, steam heat, vacuum heat treatment, and vapor heat.
Because we are removing the treatment schedules that include these
terms from the regulations, these definitions would not need to be
included in Sec. 305.1.
We are proposing to add three new definitions.
The term neutralize would be defined as, 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.
As stated in the proposed definition of neutralize, an effective
irradiation treatment does not necessarily kill a plant pest; rather,
it may render the plant pest incapable of causing an infestation, by
sterilizing it or preventing its maturation. This definition would help
to clarify that point.
The current definition of irradiation reads: ``The use of
irradiated energy to kill or devitalize organisms.'' To refer to the
new definition, we would replace the word ``devitalize'' with the word
``neutralize.'' In addition, we would correct an error in the
definition by referring to ionized energy rather than irradiated
energy.
Plant Protection and Quarantine (PPQ) would be defined as the Plant
Protection and Quarantine program of APHIS.
PPQ Treatment Manual would be defined as the document that contains
the treatment schedules that are approved for use under 7 CFR part 305.
The definition would also state that 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.
Approved Treatments (Sec. 305.2)
Most of proposed Sec. 305.2 would be drawn from current paragraph
(a) of Sec. 305.2, with modifications to reflect the relocation of the
lists of approved treatments and the treatment schedules to the
Treatment Manual. Paragraphs (b) through (v) of current Sec. 305.2
contain lists of approved treatments for various articles and would
thus be removed.
Proposed paragraph (a) of Sec. 305.2 would state that certain
commodities or articles require treatment, or are subject to treatment,
prior to the interstate movement within the United States or
importation or entry into the United States. It would also state that
treatment is required as indicated in parts 301, 318, and 319 of this
chapter, on a permit, or by an inspector.
Proposed paragraph (b) would indicate that lists of approved
treatments and approved treatment schedules are set out in the PPQ
Treatment Manual. It would also require treatments to be administered
in accordance with the treatment requirements that we would retain in
part 305 and in accordance with treatment schedules found in the PPQ
Treatment Manual.
Proposed paragraph (c), which would be retained unchanged from
current paragraph (a)(4), would indicate that APHIS is not responsible
for losses or damages incurred during treatment and would recommend
that a sample be treated first before deciding whether to treat the
entire shipment.
Proposed New Process for Adding, Revising, or Removing Treatment
Schedules (Sec. 305.3)
Proposed Sec. 305.3 would set out the notice-based processes we
are proposing to use to amend the Treatment Manual. There would be two
processes: A normal process and a process for taking immediate action.
Paragraph (a) of proposed Sec. 305.3 would describe the normal
process. Under this process, APHIS would 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 would
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.
If we have prepared documentation to support the proposed change,
we would also announce its availability via this notice. We anticipate
preparing supporting documentation for most changes to the Treatment
Manual, to indicate what data led us to propose the change in question.
However, some changes would not require such data, such as a change to
clarify a requirement or a change to remove a schedule whose use is not
authorized by another Federal agency.
After the close of the public comment period, we would issue a
notice indicating that the treatment schedule specified in the initial
notice would be added to the PPQ Treatment Manual, revised as described
in the notice, or removed from the PPQ Treatment Manual if:
No comments were received on the notice;
The comments on the notice supported our action; or
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.
If the final notice indicated that we were making the change
described in the initial notice, we would also make available, at the
Web address referred to earlier, an updated version of the
[[Page 22322]]
Treatment Manual that would reflect the addition, revision, or removal
of the particular treatment schedule.
If comments presented information that caused us to determine that
the change described in the notice was not appropriate, APHIS would
issue a notice informing the public of this determination after the
close of the comment period.
While we anticipate the process in proposed paragraph (a) to be
suitable for many changes to the PPQ Treatment Manual, certain
circumstances require that treatment schedules be added, revised, or
removed immediately. Paragraph (b) of proposed Sec. 305.3 would set
out those circumstances and describe a process for making immediate
changes to the Treatment Manual.
Paragraph (b)(1) of proposed Sec. 305.3 would describe the
circumstances in which the immediate process could be used. Under this
paragraph, treatment schedules could be immediately added to the PPQ
Treatment Manual, revised, or removed from the PPQ Treatment Manual if
any of the following circumstances applied:
PPQ has determined that an approved treatment schedule is
ineffective at neutralizing the targeted plant pest(s). For example,
when we find live pests when inspecting treated articles, we may adjust
treatment schedules to ensure that treatment is effective.
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. Some treatment
schedules contain specific instructions for their use. Upon finding
live pests when inspecting treated articles, we may determine that the
treatment must be administered differently, or that we must set out
more specific conditions for the administration of the treatment. For
example, we may determine that methyl bromide fumigation without a
tarpaulin covering the treated commodity is not effective but that the
same schedule employed with a tarpaulin will be effective.
PPQ has determined that a new treatment schedule is
effective, based on efficacy data, and that ongoing trade in a
commodity or commodities may be adversely impacted unless the new
treatment schedule is approved for use. For example, if a facility used
to perform chemical treatment on a commodity suddenly becomes
unavailable to producers in a foreign country, but a facility is
available to perform cold treatment on the commodity using a schedule
not currently approved by APHIS, we may approve the use of that
schedule to treat that commodity if efficacy data supports it.
The use of a treatment schedule is no longer authorized by
EPA or by any other Federal entity. The use of certain chemicals in
phytosanitary treatments is authorized by EPA; if EPA withdraws
approval for the use of a chemical, we must also withdraw any treatment
schedules that require the use of that chemical. Similarly, if the
Department of Health and Human Services' Food and Drug Administration
changed the maximum absorbed dose of irradiation for food, we might
need to revise our irradiation treatment requirements to reflect the
new limit.
If we determined that a change to the Treatment Manual needed to be
made immediately, we would publish in the Federal Register a notice
describing the reasons we 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
were added to the PPQ Treatment Manual or revised under this process
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). The PPQ Treatment Manual would indicate that
these treatment schedules are subject to change or removal based on
public comment. In our notice, we would 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.
After the close of the public comment period, we would issue a
notice affirming the action described in the initial notice if:
No comments were received on the notice;
The comments on the notice supported our action; or
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.
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 would make available a new version of the PPQ Treatment
Manual that would reflect the addition, revision, or removal of the
particular treatment schedule in the main body of the PPQ Treatment
Manual.
If comments on the initial notice present information that causes
us to determine that it is necessary to change a treatment schedule
added to the PPQ Treatment Manual under the immediate process or to
further revise a treatment schedule that was revised under this
process, APHIS would publish a notice in the Federal Register informing
the public of this determination after the close of the comment period
and would revise the treatment schedule accordingly.
If comments present information that causes us to determine that
the change described in the initial notice was not appropriate, APHIS
would 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.
These notice-based processes would enable us to make changes more
quickly to the treatment schedules in the PPQ Treatment Manual while
continuing to provide for public participation in the process. Changes
to the general treatment requirements that we propose to retain in part
305 would still be made through rulemaking. We invite public comment on
this approach.
Monitoring and Certification of Treatments
Proposed Sec. 305.4 would set out requirements for monitoring and
certification of treatments. Paragraph (a) of proposed Sec. 305.4 is
taken from current Sec. 305.3(a) and states that all treatments
approved under part 305 are subject to monitoring and verification by
APHIS.
Paragraph (b) of proposed Sec. 305.4 is based on current Sec.
305.3(b). The regulations in Sec. 305.3(b) require any treatment
performed outside the United States to be monitored and certified by an
inspector or an official from the national plant protection
organization (NPPO) of the exporting country. If monitored and
certified by an official of the NPPO of the exporting country, the
regulations require treated commodities to be accompanied by a
phytosanitary certificate issued by the NPPO of the exporting country
certifying that treatment was applied in accordance with APHIS
regulations. The phytosanitary certificate must be provided to an
inspector when the commodity is offered for entry into the United
States. During the entire interval between treatment and export, the
consignment must be stored and
[[Page 22323]]
handled in a manner that prevents any infestation by pests and noxious
weeds.
This proposal would amend these requirements to indicate that any
treatment performed outside the United States must be monitored and
certified by an inspector or an official authorized by APHIS, to be
consistent with the other requirements in part 305, which refer to
officials authorized by APHIS rather than NPPO officials specifically.
Proposed Sec. 305.4(b) would state that the phytosanitary
certification requirement applies when monitoring or certification
involves an official authorized by APHIS. Proposed Sec. 305.4(b) would
also refer to treatment having been conducted in accordance with APHIS
regulations, rather than to treatment having been applied, as the term
``conducted'' is more inclusive.
Chemical Treatment, Cold Treatment, Quick Freeze Treatment, and Heat
Treatment Requirements Sections (Sec. Sec. 305.5 Through 305.8)
These proposed sections are retained from the sections in part 305
that currently contain these requirements, as listed in table 2 earlier
in this document. As part of this proposal, we would make some minor
changes to these sections, as described below.
In all of these sections, we would indicate where appropriate that
treatment schedules would be found in the PPQ Treatment Manual.
In the chemical treatment requirements section (Sec. 305.5),
paragraph (c)(3) currently provides that the volume of the commodity
stacked inside a chemical treatment enclosure must not exceed \2/3\ of
the volume of the enclosure. However, there may be some circumstances
in which stacking that exceeds \2/3\ of the volume of the enclosure is
appropriate; these circumstances would be specified in the treatment
schedule. Therefore, we would amend paragraph (c)(3) to indicate that
the volume of the commodity stacked inside a chemical treatment
enclosure must not exceed \2/3\ of the volume of the enclosure unless
otherwise specified in the PPQ Treatment Manual.
In the cold treatments requirements section (proposed Sec. 305.6),
paragraph (a) currently requires, among other things, that APHIS
reapprove facilities or carriers that perform cold treatment annually,
or as often as APHIS directs. We are proposing to change this to refer
to reapproval every 3 years, or as often as APHIS directs. Three years
is an adequate interval at which to conduct reapproval if there is no
indication that the facility or carrier has problems performing cold
treatment. If reapproval at shorter intervals is necessary, we would
still have the option to require reapproval as often as APHIS directs.
Also in the cold treatment requirements section, paragraph (h)
contains additional requirements for treatments performed after arrival
in the United States. Several of these requirements call for the use of
fruit fly traps to be used near the facility, and specifically list
Jackson/methyl eugenol and McPhail traps. We are proposing to instead
refer to ``APHIS-approved fruit fly traps,'' so that it would not be
necessary to update the regulations if other effective fruit fly traps
are developed in the future.
The quick freeze treatment section (Sec. 305.17) currently lists
commodities for which quick freeze is not an authorized treatment. We
are proposing to move these requirements to Sec. 305.7 and to remove
the list of commodities for which quick freeze treatment is not
authorized. Instead, we would state that the PPQ Treatment Manual
indicates the fruits and vegetables for which quick freeze is an
authorized treatment. We would make changes to that list of fruits and
vegetables through the notice-based process described earlier in this
document.
Irradiation Treatment Requirements (Proposed Sec. 305.9)
Part 305 currently contains 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
fly; and Sec. 305.34, for regulated articles moved interstate from
Hawaii, Puerto Rico, and the U.S. Virgin Islands. The requirements in
these sections are mostly similar, and some of them are identical. As
part of revising part 305, we are proposing 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.
Current Sec. Sec. 305.31, 305.32, and 305.34 refer to approval of
certain processes and equipment both by APHIS and by the Administrator.
In proposed Sec. 305.9, we would only refer to approval by APHIS. We
would replace references to ``plant protection service'' with
references to ``national plant protection organization,'' as that is
the term used in the International Plant Protection Convention's (IPPC)
Glossary of Phytosanitary Terms (International Standard for
Phytosanitary Measures No. 5).\2\ We would also replace references to
``fruits and vegetables'' with references to ``articles,'' as
irradiation is also approved to treat commodities other than fruits and
vegetables, such as nuts, foliage, and cut flowers.
---------------------------------------------------------------------------
\2\ To view this and other standards on the Internet, go to
http://www.ippc.int/IPP/En/default.jsp and click on the ``Adopted
ISPMs'' link under the ``Standards (ISPMs)'' heading.
---------------------------------------------------------------------------
As noted previously, current Sec. 305.34 states that it applies to
irradiation treatment of certain regulated articles from Hawaii, Puerto
Rico, and the U.S. Virgin Islands. In a final rule published in the
Federal Register on January 16, 2009 (74 FR 2770-2786, Docket No.
APHIS-2007-0052) and effective on February 17, 2009, we revised the
regulations for the interstate movement of most regulated articles in
part 318. The final rule amended certain general provisions in part 318
that had applied only to Hawaii, Puerto Rico, and the U.S. Virgin
Islands and extended their applicability to Guam and the Commonwealth
of the Northern Mariana Islands. We would extend the applicability of
the irradiation regulations similarly. (For ease of reading, we will
refer to these jurisdictions collectively as ``Hawaii and U.S.
territories'' in the Background section of this document and would do
so as well in proposed Sec. 305.9.)
Currently, paragraph (a) of Sec. 305.31 sets out approved
irradiation doses for specific plant pests. Paragraph (a)(1) of Sec.
305.34 sets out approved irradiation doses for some specific fruits and
vegetables moved interstate from Hawaii, Puerto Rico, and the U.S.
Virgin Islands. In addition, paragraph (a)(1) of Sec. 305.32 refers to
treatment for fruit fly at the approved dose listed in Sec. 305.31(a),
and paragraph (a)(2) of Sec. 305.34 refers to treatment of other
regulated articles from Hawaii, Puerto Rico, and the U.S. Virgin
Islands at the doses listed in Sec. 305.31(a). We would remove this
information from the regulations and add it to the PPQ Treatment
Manual.
Proposed Sec. 305.9 would begin with a statement that irradiation,
carried out in accordance with the provisions of proposed Sec. 305.9,
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 and U.S. territories, and for any
berry, fruit, nut, or vegetable listed as a regulated article in Sec.
301.32-2(a) (i.e., the fruit fly quarantine regulations).
Proposed paragraph (a) of Sec. 305.9 would set out requirements
for the
[[Page 22324]]
location of facilities. Paragraph (a)(1) would address the location of
facilities used to treat imported regulated articles and regulated
articles moved interstate from Hawaii or U.S. territories. Requirements
for the location of facilities used to treat such articles are
currently found in Sec. 305.31(b) and Sec. 305.34(b)(1). These
requirements are identical except that Sec. 305.31(b) contains a
footnote that also allows irradiation facilities to be located at the
maritime ports of Gulfport, MS, or Wilmington, NC, or the airport of
Atlanta, GA, if certain special conditions are met, including
requirements for movement and handling of articles, fruit fly trapping,
and disposal of articles. Section 305.34(b)(1) does not contain this
footnote. We are proposing to move these conditions into the regulatory
text of proposed paragraph (a)(1). As these special conditions would be
adequate to address the pest risk associated with the movement of
regulated articles moved interstate from Hawaii or U.S. territories for
irradiation treatment at those ports, we would provide for the use of
these special conditions for both imported regulated articles and
regulated articles moved interstate from Hawaii and U.S. territories.
The footnote in current Sec. 305.31(b) requires the use of
Jackson/methyl eugenol and McPhail traps; similar to the changes
proposed for the cold treatment requirements, we would instead refer in
proposed paragraph (a)(1) to ``APHIS-approved fruit fly traps,'' so
that it will not be necessary to update the regulations if other
effective fruit fly traps are developed in the future.
Proposed paragraph (a)(2) of Sec. 305.9 would address the location
of facilities used to treat regulated articles to be moved interstate
from areas quarantined for fruit flies. The regulations in Sec. 305.32
currently do not contain a specific requirement related to the location
of facilities. Under proposed Sec. 305.9(a)(2), facilities for
irradiation of articles that are moved interstate from areas
quarantined for fruit flies could be located either within or outside
of the quarantined area. If the articles are treated outside the
quarantined area, they would have to be accompanied to the facility by
a limited permit issued in accordance with Sec. 301.32-5(b), the
paragraph in the domestic fruit fly quarantine regulations that
contains provisions for limited permits, and would have to be moved in
accordance with any safeguards determined to be appropriate by APHIS.
This provision would ensure that APHIS could impose any safeguards that
may be necessary for the safe movement of untreated articles from a
fruit fly quarantined area to a facility located outside the
quarantined area, just as APHIS has the option to impose safeguards on
the movement of untreated articles from foreign countries or from
Hawaii and U.S. territories to an irradiation facility for treatment.
Paragraph (b) of proposed Sec. 305.9 would state that the
irradiation treatment facility would have to be approved by APHIS. In
order to be approved, a facility would have to fulfill the requirements
in paragraphs (c) and (d) of proposed Sec. 305.9.
Paragraph (c) of proposed Sec. 305.9 would set out requirements
for compliance agreements. Proposed paragraph (c)(1) would set out the
compliance agreement requirements for facilities treating imported
articles; paragraphs (c)(1)(i) and (c)(1)(ii) would apply to facilities
located in the United States and to facilities outside the United
States, respectively. These paragraphs would contain the requirements
currently in paragraphs (c) and (d) of Sec. 305.31.
Proposed paragraph (c)(2) would address the compliance agreement
requirements for facilities treating regulated articles moved
interstate from Hawaii and U.S. territories. It would require a
compliance agreement with APHIS to be completed as provided in Sec.
318.13-3(d), the paragraph in part 318 that governs compliance
agreements for the movement of regulated articles from Hawaii and U.S.
territories. This requirement is currently found in Sec.
305.34(b)(2)(iii).
Proposed paragraph (c)(3) addresses the compliance agreement
requirements for facilities treating regulated articles to be moved
interstate from areas quarantined for fruit flies. It would require a
compliance agreement with APHIS to be completed as provided in Sec.
301.32-6. This requirement is currently found in Sec. 305.32(a)(3).
Proposed paragraph (d) would set out requirements for certification
of an irradiation treatment facility. The introductory text of
paragraph (d) would contain the certification and recertification
requirements currently found in the introductory text of Sec.
305.31(e), paragraph (a)(4) of Sec. 305.32, and paragraph (b)(2)(iv)
of Sec. 305.34.
Under proposed paragraph (d), the irradiation treatment facility
would have to be certified by APHIS. This language is drawn from
current Sec. 305.31(e). Unlike Sec. 305.31(e), Sec. Sec.
305.32(a)(4) and 305.34(b)(2)(iv) refer to certification by PPQ and
require annual recertification. We have determined that it is not
necessary to require annual recertification for facilities used to
treat regulated articles moved interstate from Hawaii and U.S.
territories or regulated articles moved interstate from areas
quarantined for fruit flies, in the absence of one of the events
currently listed in the regulations as a reason for recertification.
Recertification would be required in the event of an increase or
significant decrease in the amount of radioisotope, a major
modification to equipment that affects the delivered dose, or a change
in the owner or managing entity of the facility. Only the regulations
in Sec. 305.31(e) currently include a change in the owner or managing
entity of the facility as a reason for recertification; we have
determined that this requirement would be appropriate for irradiation
facilities used to treat regulated articles moved interstate from
Hawaii and U.S. territories and regulated articles to be moved
interstate from areas quarantined for fruit flies as well, to ensure
that currently certified facilities continue to comply with the
regulations under new ownership or management. (The regulations
currently refer only to a decrease in the amount of radioisotope;
because the amount of radioisotope decreases in very small amounts
during treatment, we are proposing to add the word ``significant'' to
better characterize the type of decrease that would require
recertification.)
Recertification also could be required in cases where a significant
variance in dose delivery has been measured by the dosimetry system.
The requirements in Sec. Sec. 305.32(a)(4) and 305.34(b)(2)(iv) refer
to recertification in cases where a significant variance in dose
delivery is indicated; the language in Sec. 305.31(e), which we use in
this proposal, provides helpful additional specificity.
Proposed paragraphs (d)(1) through (d)(3) set out requirements for
certification. In order to be certified, a facility would have to:
Be capable of administering the minimum absorbed ionizing
radiation doses specified in the PPQ Treatment Manual to the regulated
articles. This requirement is drawn from Sec. Sec. 305.31(e)(1),
305.32(a)(1), and 305.34(b)(2)(i). We would add the reference to the
PPQ Treatment Manual to be consistent with the other changes in this
proposal.
Be constructed so as to provide physically separate
locations for treated and untreated fruits and vegetables, except that
fruits and vegetables traveling by conveyor directly into the
irradiation chamber may pass through an area that would otherwise be
separated. The locations would have to be separated by a permanent
physical barrier such as a wall or chain link fence
[[Page 22325]]
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. This requirement is drawn from Sec. 305.31(e)(2). The
same requirements are included in Sec. Sec. 305.32(a)(2) and
305.34(b)(2)(ii), except that these paragraphs do not provide for the
use of some means other than a physical barrier that would be approved
during certification to prevent reinfestation of articles and spread of
pests. Providing such an option for irradiation facilities treating
regulated articles moved interstate from Hawaii and U.S. territories
and regulated articles to be moved interstate from areas quarantined
for fruit flies would increase flexibility for such facilities without
increasing risk, since any other means used to prevent reinfestation
would be subject to APHIS approval during certification.
If the facility is to be used to treat imported articles
and is located in the United States, the facility would only be
certified if APHIS determines that regulated articles would 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. This requirement is drawn from
Sec. 305.31(e)(3). It is not necessary to include a similar
requirement for facilities treating articles moved interstate from
Hawaii and U.S. territories or articles moved interstate from an area
quarantined for fruit flies, as their movement is governed by a limited
permit; before granting a limited permit, APHIS would have to determine
that the movement of the articles could be accomplished safely.
Paragraph (e) of proposed Sec. 305.9 would set out requirements
for monitoring and interagency agreements. The introductory text of
proposed paragraph (e) would state that treatment must be monitored by
an inspector and that 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. This requirement is drawn from current Sec. Sec.
305.31(f), 305.32(b), and 305.34(b)(3).
Proposed paragraph (e)(1) would set out requirements for monitoring
and interagency agreements for irradiation facilities located in
foreign countries. These requirements would be moved from Sec.
305.31(f). These requirements currently apply to any facility treating
imported articles, and they are somewhat more detailed and rigorous
than the monitoring requirements for irradiation facilities treating
articles moved interstate from Hawaii and U.S. territories and from
areas quarantined for fruit flies. The additional requirements are
necessary 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 of articles treated
within the United States does not.
Irradiation treatment of imported articles can be conducted either
in the country of origin or within the United States, but the detailed
requirements for monitoring and interagency agreements in Sec.
305.31(f) only apply to facilities located in foreign countries, for
the reasons described above. Therefore, we are proposing to clearly
indicate in the regulatory text that these requirements only apply to
irradiation facilities located in foreign countries, not necessarily
all facilities that treat imported articles.
We would make one change to the requirements for monitoring and
interagency agreements for facilities located in foreign countries. The
trust fund agreement requirements refer to the NPPO of the country in
which the irradiation facility is located entering into a trust fund
with APHIS. Often, we enter into the trust fund with a private export
group that operates the facility. Therefore, we would amend the
existing text describing trust fund agreements to refer to entering
into the agreement either with the NPPO or with a private export group.
This change would be consistent with the general language governing
trust fund agreements related to the importation of fruits and
vegetables in Sec. 319.56-6.
Proposed paragraph (e)(2) would set out requirements for monitoring
and interagency agreements for irradiation facilities located within
the United States. This paragraph would contain the current
requirements for irradiation facilities treating articles moved
interstate from areas quarantined for fruit flies and from Hawaii and
U.S. territories in Sec. Sec. 305.32(b) and 305.34(b)(3),
respectively; those paragraphs are identical. For the reasons described
above, we have determined that these requirements would also be
appropriate for irradiation facilities located within the United States
that are used to treat imported articles.
Proposed paragraph (f) of Sec. 305.9 would set out packaging
requirements. Under proposed paragraph (f)(1), irradiated articles
would not be allowed to be packaged for shipment in a carton with
nonirradiated articles. This requirement is drawn from current
Sec. Sec. 305.31(g)(1) and 305.34(b)(2), which apply to articles
imported into the United States and articles moved interstate from
Hawaii, Puerto Rico, and the U.S. Virgin Islands, respectively; we have
determined that it is appropriate for articles moved interstate from
areas quarantined for fruit flies as well, as it helps to reduce the
risk of reinfestation of treated articles.
Current paragraph (g)(1) of Sec. 305.31 also requires irradiated
articles to be shipped in the same cartons in which they are treated;
the irradiation treatment regulations for articles moved interstate
from Hawaii, Puerto Rico, and the U.S. Virgin Islands and for articles
moved interstate from areas quarantined for fruit flies do not contain
such a requirement. We have determined that requiring irradiated
articles to be shipped in the same cartons in which they are treated is
unnecessary. The requirement is intended to prevent untreated articles
from being shipped and to prevent treated articles from being infested
with fruit flies after treatment, but other requirements in the
irradiation treatment regulations (such as those discussed directly
above and below) adequately address this issue. Additionally, treatment
is always monitored by an inspector, who will be able to ensure that
adequate safeguarding measures are practiced. Accordingly, the
irradiation treatment regulations proposed here do not include the
same-carton requirement.
The current packaging requirements in the irradiation treatment
regulations specifically address fruit flies. However, irradiation
treatment is approved for pests other than fruit flies, and some
commodities that are irradiated are not fruit fly hosts. Therefore, we
are proposing to amend the current requirements to refer to packaging
sufficient to prevent the infestation or reinfestation of the treated
articles by the pests of concern, rather than fruit flies specifically.
Proposed paragraph (f)(2) sets out packaging requirements for
imported articles treated prior to arrival in the United States; for
regulated articles moved interstate from Hawaii or U.S. territories and
irradiated prior to arrival in the mainland United States; and for
regulated articles to be moved interstate from areas quarantined for
fruit flies that are treated within the quarantined area. The
requirements in proposed paragraph (f)(2) are drawn from Sec. Sec.
305.31(g)(3), 305.32(c), and 305.34(b)(4)(i).
[[Page 22326]]
Under this paragraph, the articles to be irradiated would have to
be packaged either:
In insect-proof cartons that have no openings that will
allow the entry of the pests of concern. The cartons would have to be
sealed with seals that will visually indicate if the cartons have been
opened. The cartons could be constructed of any material that prevents
entry or oviposition (if applicable) by the pests of concern into the
articles in the carton; or
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 would have
to 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.
These two options are drawn from current Sec. 305.31(g)(3), which
applies to imported commodities treated prior to arrival in the United
States. Current Sec. Sec. 305.32(c) and 305.34(b)(4)(i), which apply,
respectively, to articles treated in Hawaii, Puerto Rico, or the U.S.
Virgin Islands and to articles treated in an area quarantined for fruit
fly, do not provide the option to use noninsect-proof cartons;
providing this option for treatment of those articles increases
flexibility without increasing risk, since APHIS would have to approve
any room used to store treated articles in noninsect-proof cartons.
Each pallet-load of cartons containing the fruits and vegetables
would have 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.
These requirements are drawn from current Sec. Sec.
305.31(g)(3)(ii), 305.32(c)(2), and 305.34(b)(4)(i)(B). Current Sec.
305.31(g)(3)(ii) states that the wrapping requirements are intended to
preserve the identity of treated lots. Instead of referring to the
identity of the treated lots, we are proposing to refer to the
integrity of the treated lots, as the requirements are intended to
allow treated lots to be easily identifiable and separated from
untreated lots.
Packaging would have to be labeled with treatment lot numbers,
packing and treatment facility identification and location, and dates
of packing and treatment. This requirement is drawn from current
Sec. Sec. 305.31(g)(3)(iii), 305.32(c)(3), and 305.34(b)(4)(i)(C).
Under current Sec. 305.31(g)(3)(iii), pallets of imported articles
that are treated prior to arrival in the United States must remain
intact as one unit until entry into the United States and may have one
such label per pallet, and pallets that are broken apart into smaller
units prior to or during entry into the United States must have the
required label information on each individual carton. We would retain
these requirements in proposed Sec. 305.9(f)(2)(iii)(A) and would
extend their applicability in proposed Sec. 305.9(f)(2)(iii)(B) to
articles moved interstate from Hawaii and U.S. territories that are
treated prior to arrival in the mainland United States. We are also
proposing to require label information on individual cartons if the
pallets will be broken apart after entry into the mainland United
States as well. These requirements would ensure that we can conduct
traceback to the treatment facility if necessary and would also
indicate to inspectors that the articles have been subject to an
approved treatment and have moved under certificate or limited permit,
whichever is applicable.
Similar requirements for labeling of cartons within pallets are not
necessary for articles moved interstate from areas quarantined for
fruit flies and treated prior to interstate movement, because the
articles enter commerce directly after treatment, meaning that there is
no gap in distance or time between treatment and distribution that
would necessitate additional information for traceback. In addition,
because such articles are moved directly into commerce, they are not
typically palleted.
Proposed paragraph (f)(3) of Sec. 305.9 would set out the
requirements for packaging for articles imported to be irradiated upon
arrival in the United States, moved interstate to be irradiated upon
arrival in the mainland United States, or moved interstate from areas
quarantined for fruit flies to be irradiated. Under this paragraph,
such articles would have to 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 could be constructed of any material that prevents the pests of
concern from exiting the carton. These requirements are drawn from
current Sec. 305.31(g)(2), which applies to articles irradiated after
importation into the United States; we have determined that they are
appropriate for regulated articles irradiated after interstate movement
from Hawaii and U.S. territories and regulated articles irradiated
after interstate movement from areas quarantined for fruit flies as
well, in order to provide additional protection against the
introduction of quarantine pests. Current Sec. 305.31(g)(2) refers to
preventing the entry of the pests of concern into the cartons; we are
proposing to refer to the exit of those pests, because this measure is
designed to prevent pests that have infested the articles from being
introduced into the United States before the articles are treated.
Proposed paragraph (f)(3) would also require that cartons of such
articles be shipped in shipping containers sealed prior to their
shipment with seals that will visually indicate if the shipping
containers have been opened. This requirement is drawn from Sec.
305.34(b)(4)(ii), which applies to articles treated before they are
moved interstate from Hawaii, Puerto Rico, or the U.S. Virgin Islands
into the United States. We have determined that this requirement is
appropriate for imported articles treated after importation and
articles moved interstate from areas quarantined for fruit flies that
are treated after movement as well, because it provides additional
protection against the introduction of quarantine pests.
The labeling requirements in Sec. 305.34 also include provisions
prohibiting the interstate movement of litchi and longan from Hawaii
into Florida and requiring all cartons in which litchi or longan are
packed to be stamped ``Not for importation into or distribution in
FL.'' These provisions would be better placed in the regulations
governing the interstate movement of fruits and vegetables in part 318,
since the labeling requirements here are not related to irradiation
treatment but rather to the risk posed by the litchi rust mite, which
is not addressed by irradiation. Accordingly, we are proposing to amend
the table of regulated articles allowed interstate movement under
specified conditions in Sec. 318.13-16 by adding entries for litchi
and longan from Hawaii; these entries would indicate that the
interstate movement of litchi and longan from Hawaii is subject to the
distribution restriction and labeling requirements that are currently
found in Sec. 305.34. We would also change the required stamp to refer
correctly to movement into Florida, rather than importation.
Proposed paragraph (g) of Sec. 305.9 would require that containers
or vans that will transport treated articles be free of pests prior to
loading the treated articles. This requirement is drawn from
[[Page 22327]]
current Sec. 305.31(h), which applies to imported articles that have
been treated with irradiation. We are also proposing to apply this
requirement to the transportation of treated articles moved interstate
from Hawaii and U.S. territories and treated articles to be moved
interstate from areas quarantined for fruit flies, as it provides
additional phytosanitary security.
Proposed paragraph (h) of Sec. 305.9 would contain the
phytosanitary certification requirement for imported articles that is
currently found in Sec. 305.31(i). However, we would amend this
requirement to refer to consignments rather than shipments, as
``consignments'' is the term used in the IPPC Glossary of Phytosanitary
Terms.
Paragraph Sec. 305.34(b)(7) of the regulations governing
irradiation treatment of articles moved interstate from Hawaii, Puerto
Rico, and the U.S. Virgin Islands contains specific requirements for
certification or limited permits for the interstate movement of several
commodities that apply in addition to irradiation treatment. For
example, breadfruit and jackfruit, which have specific requirements for
certification and limited permits in Sec. Sec. 305.34(b)(7)(i)(C) and
305.34(b)(7)(ii)(C), respectively, must be inspected and found to be
free of various pests, treated with irradiation for fruit flies,
subjected to a treatment for external feeders or originate from an
orchard or growing area that has been treated with a broad-spectrum
insecticide, free of stems and leaves, and originate from an orchard
that was treated with a fungicide appropriate for the fungus
Phytophthora tropicalis or subjected to a post-harvest fungicidal dip
appropriate for that fungus. These requirements are not related to
irradiation treatment, but rather address other pest risks that
irradiation treatment does not mitigate. Accordingly, we are proposing
to move the specific certification and limited permit requirements
currently found in Sec. 305.34(b)(7)(i)(A) through (H) and Sec.
305.34(b)(7)(ii)(A) through (D) to part 318. Specifically:
The certification and limited permit requirements for
litchi from Hawaii, which are found in paragraphs (b)(7)(i)(A) and
(b)(7)(ii)(A) of Sec. 305.34, respectively, refer only to inspection
for freedom from pests. As movement of any fruit or vegetable from
Hawaii is subject to inspection for freedom from pests under Sec.
318.13-3, it would not be necessary to retain this specific requirement
in the regulations.
The certification and limited permit requirements for
sweetpotatoes, which are found in paragraphs (b)(7)(i)(B) and
(b)(7)(ii)(B) of Sec. 305.34, respectively, would be added to Sec.
318.13-25, which contains requirements for the interstate movement of
sweetpotatoes from Hawaii with vapor heat treatment.
The certification and limited permit requirements for
breadfruit and jackfruit, which are found in paragraphs (b)(7)(i)(C)
and (b)(7)(ii)(C) of Sec. 305.34, respectively; the certification and
limited permit requirements for fresh pods of cowpea and its relatives,
which are found in paragraphs (b)(7)(i)(D) and (b)(7)(ii)(D) of Sec.
305.34, respectively; and the certification requirements for dragon
fruit, mangosteen, melon, and moringa pods, which are found in
paragraphs Sec. 305.34(b)(7)(i)(E) through (b)(7)(i)(H), respectively,
would be included in a new Sec. 318.13-26. This new section would
indicate explicitly that irradiation treatment is required for these
commodities, in addition to the other requirements.
In addition, because we are proposing to remove specific
irradiation doses from the regulations, as discussed earlier, we would
amend the specific certification and limited permit provisions by
removing references to specific irradiation doses and replacing them
with references to irradiation treatment for certain pests. For
example, in order to be certified for interstate movement under current
Sec. 305.34(b)(7)(i)(C), breadfruit and jackfruit must be inspected in
Hawaii and found to be free of certain pests and treated at the 150
gray dose to neutralize fruit flies. Inspection for plant pests of the
class Insecta (except pupae and adults of the order Lepidoptera) is
unnecessary if the fruits are treated at the 400 gray dose, which is
approved to neutralize those plant pests. Rather than include the doses
in the revised irradiation treatment requirements, we would simply
refer in the new Sec. 318.13-26 to treatment at a dose approved to
neutralize fruit flies or at a dose approved to neutralize all plant
pests of the class Insecta, except pupae and adults of the order
Lepidoptera. We would also remove references to treatment schedule
T102-c, which is a soapy water dip treatment for external pests, and
instead refer to treatment in accordance with part 305 for external
pests. This would allow the regulations to conform with any changes we
might make to the approved irradiation doses or other treatments
through the notice-based process outlined earlier in this proposal.
General certification and limited permit provisions for articles
moved interstate from Hawaii and U.S. territories are found in Sec.
318.13-3; similarly, general certification and limited permit
provisions for articles moved interstate from areas quarantined for
fruit flies are found in Sec. 301.32-5 of the domestic fruit fly
quarantine regulations. It is not necessary to duplicate those general
provisions in the irradiation treatment requirements.
Proposed paragraph (i) of Sec. 305.9 would require that the
regulated articles receive the minimum absorbed ionizing radiation dose
specified in the PPQ Treatment Manual. The similar requirements
currently found in Sec. Sec. 305.32(d), for articles moved interstate
from areas quarantine for fruit flies, and 305.34(b)(5), for articles
moved interstate from Hawaii, Puerto Rico, and the U.S. Virgin Islands,
refer to receiving the dose specified in the regulations; we would
change this reference as part of moving the lists of approved
treatments and schedules to the PPQ Treatment Manual. The regulations
for the irradiation treatment of imported articles do not contain a
similar requirement, although it is implied; we believe it would be
helpful to make the requirement explicit for all types of articles.
Proposed paragraph (j) of Sec. 305.9 sets out requirements for
dosimetry systems at the irradiation facility. Such requirements are
currently contained in Sec. Sec. 305.31(j), 305.32(e), and
305.34(b)(6). Although there are wording differences among the current
requirements for dosimetry systems, they are substantively identical,
and we have incorporated them into the proposed text with minor changes
to ensure consistency.
Proposed paragraph (j)(1) would require dosimetry to indicate the
doses needed to ensure that all the articles will receive the minimum
dose prescribed.
Proposed paragraph (j)(2) would require the absorbed dose, as
measured using an accurate dosimetry system, to meet or exceed the
absorbed dose for the pest(s) of concern required by the PPQ Treatment
Manual. The current dosimetry requirements refer to receiving the dose
specified in the regulations; we would change this reference as part of
moving the lists of approved treatments and scheduled to the PPQ
Treatment Manual.
Proposed paragraph (j)(3) would require the facility operator, when
designing the facility's dosimetry system and procedures for its
operation, to address guidance and principles from the International
Standards Organization/American Society for Testing and Materials
standard or an equivalent standard recognized by APHIS.
[[Page 22328]]
Proposed paragraph (k) of Sec. 305.9 set outs requirements for
recordkeeping. These requirements are copied from Sec. Sec. 305.31(k),
305.32(f), and 305.34(b)(8), which are identical.
Proposed paragraph (l) of Sec. 305.9 sets out requirements for
requesting certification and inspection of a facility. Under this
paragraph, persons requesting certification of an irradiation treatment
facility would have to 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
would have to 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 would make a
personal inspection of the facility to determine whether it complies
with the standards of proposed Sec. 305.9.
These requirements are taken from current Sec. 305.31(l), which
applies to facilities used to treat imported articles. Similar
requirements are contained in Sec. Sec. 305.32(g), which applies to
facilities used to treat articles moved interstate from areas
quarantined for fruit flies, and 305.34(c), which applies to facilities
used to treat articles moved interstate from Hawaii, Puerto Rico, and
the U.S. Virgin Islands. Proposed paragraph (l) differs in that it
refers to the certification of a facility, rather than to approval of a
facility. Current Sec. Sec. 305.32(g) and 305.34(c) also do not
include the requirement that the initial request for certification
include the information described earlier. The submission of such
information in requests for certification of irradiation facilities
used to treat regulated articles moved interstate from Hawaii and U.S.
territories or regulated articles to be moved interstate from areas
quarantined for fruit flies would allow us to more efficiently evaluate
requests for certification.
In this proposal, we would also update the address of the Center
for Plant Health Science and Technology, which is now located at the
address given above.
Proposed paragraph (m) of Sec. 305.9 sets out provisions for
denial and withdrawal of certification. These requirements are taken
from current Sec. 305.31(m). Except for referring to approval of a
facility rather than certification, the requirements for denial and
withdrawal in Sec. Sec. 305.32(h) and 305.34(d) are identical to the
requirements in proposed Sec. 305.31(m).
Proposed paragraph (n) of Sec. 305.9 informs the reader that the
Department is not responsible for damage to treated articles. This
proposed paragraph is copied from current Sec. Sec. 305.31(n),
305.32(i), and 305.34(e), which are identical.
The proposed changes to the irradiation treatment regulations would
make the requirements more consistent across different types of
facilities and would eliminate redundant text. We invite public comment
on these changes.
Removal of Treatment Schedules From 7 CFR Parts 301 and 319
Although part 305 serves as the main source for treatment schedules
authorized under 7 CFR chapter III, there are also some other treatment
schedules contained in parts 301 and 319. As part of this proposal, we
would remove those schedules from the regulations and (if necessary)
add them to the PPQ Treatment Manual. The schedules we are proposing to
remove from the regulations are:
Fumigation and cold treatment schedules for pine shoot
beetle in paragraphs (a) through (c) of Sec. 301.50-10;
Various treatments for citrus canker in Sec. 301.75-11;
Chemical treatments in the appendix to the subpart for
imported fire ant (Sec. Sec. 301.81 through 301.81-10);
Heat and disinfection treatments for sugarcane diseases in
Sec. 301.87-10;
Cleaning and disinfection treatments for Karnal bunt in
Sec. 301.89-13;
Heat treatments for Phytophthora ramorum in Sec. 301.92-
10;
A methyl bromide fumigation treatment for Unshu oranges
from Japan and Korea in Sec. 319.28(b)(5);
Heat treatment and fumigation schedules for regulated wood
packing material in Sec. 319.40-3(b)(1);
Heat treatment, fumigation, and surface pesticide
treatments for regulated wood in Sec. 319.40-7(c) through (f);
Treatments for disinfection of broomcorn and broomcorn
products in Sec. 319.41-5a;
A specific temperature requirement for quick freeze
treatment in Sec. 319.56-12;
Disinfection treatments for Karnal bunt in paragraphs
(d)(3)(i) through (d)(3)(iii) of Sec. 319.59-4; and
Fumigation treatment schedules for cut flowers in
paragraph (c)(2) of Sec. 319.74-2.
Under the heading ``4. Imported-Fire-Ant-Free Nursery--
Containerized Plants Only,'' the appendix to the imported fire ant
subpart describes a systems approach for ensuring nursery freedom from
imported fire ant and provides conditions under which containerized
nursery stock may be certified for interstate movement under Sec.
301.81-5. We would move this systems approach to a new section Sec.
301.81-11, moving the chemical treatment schedules included in the
systems approach to the PPQ Treatment Manual and making minor editorial
changes to accommodate the movement of the systems approach
requirements into the new section. This change would thus remove the
appendix from the imported fire ant subpart.
Because we would remove the schedules listed above from the
regulations, we would also need to update references to those schedules
elsewhere in the regulations. The specific changes we are consequently
proposing can be found in the regulatory text at the end of this
document.
We would retain in the regulations treatments that are not intended
for use on regulated articles but rather for use on premises, such as
the malathion or spinosad bait spray treatments in Sec. 301.32-10(b)
for premises in fruit fly quarantined areas.
Miscellaneous Changes
In addition to removing treatment schedules, the changes proposed
here would also make it necessary to update several references to
treatments throughout 7 CFR chapter III. For example, several
requirements within ``Subpart--Fruits and Vegetables'' (Sec. Sec.
319.56-1 through 319.56-48) refer to authorized treatments listed in 7
CFR part 305. As we are proposing to revise it, part 305 would not list
specific authorized treatments; it would instead refer the reader to
the PPQ Treatment Manual for specific approved treatments. Accordingly,
we would amend references to authorized treatments listed in 7 CFR part
305 to refer instead to treatment in accordance with 7 CFR part 305.
Other changes are required when the regulatory text refers to
specific sections or treatments in the current 7 CFR part 305; for
example, the ``Subpart--Hawaiian Fruits, Vegetables, and Flowers''
regulations sometimes refer specifically to irradiation treatment in
accordance with Sec. 305.34. These references would be amended to
refer
[[Page 22329]]
generally to part 305, rather than to a specific section or treatment.
All of the changes we are making to ensure consistency with the
proposed changes can be found in the regulatory text at the end of this
document.
Some requirements in 7 CFR chapter III refer to treatment of
articles, but do not refer specifically to treatment in accordance with
part 305. We are proposing to include references to treatment in
accordance with part 305 in existing treatment requirements in
Sec. Sec. 318.47-3(a), 319.8-23(a)(1), and 319.55-6(b)(1).
Some other provisions in 7 CFR chapter III refer generally to
treatment as well. Within part 330, which addresses the risks posed by
movement of plant pests; soil, stone, and quarry products; and garbage,
Sec. Sec. 330.106(a) and 330.300 refer to treatment as a mitigation an
inspector can direct to be employed in certain circumstances. In part
352, which contains provisions for safeguarding plants and plant
products that transit the United States, Sec. 352.10(b)(2)(viii)
refers to the availability of treatment facilities as a factor in
granting a transit permit, and Sec. 352.30 refers to treatment as may
be required by an inspector for shipping containers used to transport
untreated citrus in order to prevent plant pest dissemination. We are
proposing to amend these references to ``treatment'' to refer
specifically to treatment in accordance with part 305.
The regulations for the interstate movement of sweetpotatoes from
Hawaii with vapor heat treatment in Sec. 318.13-25 contain packaging
requirements similar to those for irradiated articles moved interstate
from Hawaii. These packaging requirements refer to preventing
infestation by fruit flies, but sweetpotato is not a host of fruit
flies. For the same reasons discussed earlier with respect to the
irradiation packaging requirements, we would amend these requirements
to refer instead to ``the pests of concern.''
Executive Order 12866 and Regulatory Flexibility Act
This proposed rule has been reviewed under Executive Order 12866.
The 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.
APHIS is proposing amendments to 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 proposing to remove the lists of authorized treatments and
treatment schedules from part 305, while retaining the general
requirements for performing treatments and treatment facilities. We
would remove treatment schedules from other places where they are
currently found in parts 301 and 319 as well. Treatment schedules would
instead be found in the PPQ Treatment Manual. We are also proposing to
establish a new process to make changes to the lists of approved
treatments and the treatment schedules and to inform the public and
solicit comments on the changes. We would also establish a process by
which we could make immediate changes to the lists of approved
treatments and to the treatment schedules, and establish criteria for
when we could use this process. The current regulations do not address
situations where there is an immediate need to withdraw treatments,
modify treatments, or apply treatments differently. Finally, we would
harmonize the separate requirements for performing irradiation
treatment for imported articles, articles moved interstate from Hawaii,
Puerto Rico, and the U.S. Virgin Islands, and articles moved interstate
from an area quarantined for fruit flies. These changes would simplify
and expedite our processes for adding, changing, and removing treatment
schedules while continuing to provide for public participation in the
process. These changes would 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 proposed 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 would
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 would 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 and/or diseases. This proposed
rule would 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
[[Page 22330]]
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.\3\ All types of farms are considered small if
they have annual receipts of $0.75 million or less. In 2002, more than
99 percent of oilseed and grain farms, more than 99 percent of
vegetable and melon farms, more than 99 percent of fruit and tree nut
farms, more than 99 percent of greenhouse, nursery, and floriculture
producers, and more than 99 percent of other crop farms were considered
small by SBA standards.\4\
---------------------------------------------------------------------------
\3\ 2002 Economic Census. Department of Commerce. U.S. Bureau of
the Census. North American Industry Classification System (NAICS)
Categories. 424480--Fresh fruit & Vegetable merchant wholesalers;
424510--Grain & field bean merchant wholesalers; 424930--Flower,
nursery stock, and florists' supplies merchant wholesalers.
\4\ 2002 Census of Agriculture. US Department of Agriculture.
National Agricultural Statistics Service. NAICS Categories--1111:
Oilseed & Grain farming; 1112: Vegetable and melon farming; 1113:
Fruit and tree nut farming; 1114: Greenhouse, nursery & Floriculture
production; and 1119: Other Crop farming.
---------------------------------------------------------------------------
Treatments are applicable to a wide variety of products including
fruits, vegetables, live plants, bulbs, seeds, grains, logs, lumber,
and other plants and plant products in a wide variety of circumstances.
Vast quantities of treated products move into and through the United
States annually. The United States is among the top producers and
consumers of plants and plant products. U.S. per capita use of fruit
and tree nuts totals nearly 300 pounds each year, ranking third in per
capita consumption of major food groups, next to dairy and vegetables.
Oranges, apples, grapes, and bananas are the most popular fruit while
almonds, pecans, and walnuts are the most preferred tree nuts. Annual
per capita use of all vegetables and melons averaged 445 pounds during
the first 5 years of the 2000s.
Table 3--U.S. Production Value of Selected Crops, 2004-2006
[$ 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 $12 billion in 2006.
Table 4--U.S. Imports of Plants and Plant Products, 2004-2006
[$ 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
Fruit and nuts:
Bananas............................... 1,102 1,134 1,201
Citrus, fresh......................... 307 356 407
[[Page 22331]]
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 proposed
in this rule would 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 proposed rule
would 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 would
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 proposed rule has been reviewed under Executive Order 12988,
Civil Justice Reform. If this proposed rule is adopted: (1) All State
and local laws and regulations that are inconsistent with this rule
will be preempted; (2) no retroactive effect will be given to this
rule; and (3) administrative proceedings will not be required before
parties may file suit in court challenging this rule.
Paperwork Reduction Act
This proposed rule contains no new information collection or
recordkeeping requirements under the Paperwork Reduction Act of 1995
(44 U.S.C. 3501 et seq.).
Lists 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.
Accordingly, we propose to amend 7 CFR chapter III as follows:
PART 301--DOMESTIC QUARANTINE NOTICES
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).
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]
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.
4. Section 301.50-10 is amended as follows:
a. By revising paragraph (a) to read as set forth below.
b. By removing paragraphs (b) and (c).
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.
* * * * *
[[Page 22332]]
Sec. 301.75-4 [Amended]
5. In Sec. 301.75-4, paragraphs (d)(2)(i)(C), (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]
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]
7. In Sec. 301.75-7, paragraphs (a)(3), (c)(1)(ii), and (c)(2)(v)
are amended by removing the words ``Sec. 301.75-11(a) of this
subpart'' and adding the words ``part 305 of this chapter'' in their
place; and paragraph (c)(2)(iv) is amended by removing the words
``Sec. 310.75-11(d) of this subpart'' and adding the words ``part 305
of this chapter'' in their place.
Sec. 301.75-8 [Amended]
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]
9. Section 301.75-11 is removed and reserved.
Sec. 301.81-4 [Amended]
10. Section 301.81-4 is amended as follows:
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.
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''.
11. Section 301.81-5 is amended as follows:
a. In paragraph (a)(3)(ii), at the end of the paragraph, by
removing the word ``or''.
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'' in their place; and by adding the word ``or'' at the end of
the paragraph.
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 of this subpart.
* * * * *
Sec. 301.81-6 [Amended]
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.
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 survey visually
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 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 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 180 days be either:
(A) Repotted in treated potting soil media;
(B) Retreated in accordance with part 305 of this chapter at 180-
day intervals; 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.
[[Page 22333]]
(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.
Sec. 301.87-5 [Amended]
14. 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]
15. Section 301.87-10 is removed and reserved.
Sec. 301.89-5 [Amended]
16. In Sec. 301.89-5, paragraph (b) is 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]
17. 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]
18. 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]
19. 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]
20. Section 301.89-13 is removed and reserved.
Sec. 301.92-5 [Amended]
21. 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]
22. Section 301.92-10 is removed and reserved.
23. 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.
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. The use of ionized energy to kill or neutralize
organisms.
Methyl bromide. A colorless, odorless biocide used to fumigate a
wide range of commodities.
Neutralize. 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.
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.
[[Page 22334]]
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 a
commodity or commodities 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 listed
in a separate section of 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;
(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.
[[Page 22335]]
(b) Any treatment performed outside the United States must be
monitored and certified by an inspector or an official authorized by
APHIS. If monitoring and certification involves an official authorized
by APHIS, the treated commodities must be accompanied by a
phytosanitary certificate issued by the national plant protection
organization of the exporting country certifying that treatment was
conducted in accordance with APHIS regulations. The phytosanitary
certificate must be provided to an inspector when the commodity is
offered for entry into the United States. 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) Approval 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 approved by
APHIS. Reapproval 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 approved, 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] longitude
and east of 104[deg] latitude 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.
(3) Be structurally sound and adequate to maintain required
temperatures.
(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
[[Page 22336]]
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 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.
[[Page 22337]]
(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.
(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. 307.8 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, 318.13-
[[Page 22338]]
4a, or 318.58-4a, respectively. 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
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) 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 fruit flies that may be associated with the
articles to be irradiated. In the importer compliance agreement, the
importer
[[Page 22339]]
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 or a significant decrease in the amount of radioisotope, 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\
---------------------------------------------------------------------------
\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.
---------------------------------------------------------------------------
(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 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:
(i) 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.
(ii) 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.
(iii) 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 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
[[Page 22340]]
account until needed, at the option of the NPPO or the private export
group .
(2) Irradiation facilities located within the United States.
Facilities located within the United States that carry out continual
irradiation operations must notify an inspector at least 24 hours
before the date of operations. Facilities that carry out periodic
irradiation operations must notify an inspector of scheduled operations
at least 24 hours before scheduled operations.\2\
---------------------------------------------------------------------------
\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 wrapped before
leaving the irradiation facility in one of the following ways:
(A) With polyethylene shrink wrap;
(B) With net wrapping; or
(C) With strapping so that each carton on an outside row of the
pallet load is constrained by a metal or plastic strap.
(iii) Packaging must be labeled with 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 commodities must be free of pests prior to loading the treated
commodities.
(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 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 certification and inspection of facility. Persons
requesting 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
[[Page 22341]]
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 listed plant pests.
From the literature available, the fruits and vegetables 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
24. 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]
25. 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.
26. Section 318.13-16 is amended as follows:
a. In the table in paragraph (a), by adding, under Hawaii, new
entries for litchi and longan to read as set forth below.
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 district of Additional
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.''
* * * * *
Sec. 318.13-22 [Amended]
27. 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,
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.
* * * * *
28. 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
[[Page 22342]]
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 wrapped 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 so that each carton on an outside row of the
pallet load is constrained by a metal or plastic strap.
(C) Packaging must be labeled with 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)
29. 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 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
[[Page 22343]]
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]
30. 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--[AMENDED]
31. 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.
32. In Sec. 319.8-23, paragraph (a)(1) is revised to read as
follows:
Sec. 319.8-23 Treatments.
(a)(1) Vacuum fumigation as required in this subpart must be
conducted in accordance with part 305 of this chapter.
* * * * *
Sec. 319.28 [Amended]
33. Section 319.28 is amended as follows:
a. In paragraph (b)(5), by adding the words ``in accordance with
part 305 of this chapter'' after the words ``fumigated with methyl
bromide''; and by removing the second sentence.
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]
34. 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.
35. 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.
* * * * *
36. Section 319.40-5 is amended as follows:
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.
b. 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.
c. 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.
d. 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.
e. 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.
f. 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.
g. In paragraph (d), by removing the citation ``Sec. 319.40-7(f)''
and adding the words ``part 305 of this chapter'' in its place.
h. In paragraph (f), by removing the citation ``Sec. 319.40-7(c)''
and adding the words ``part 305 of this chapter'' in its place.
i. By revising paragraph (l)(3) to read as set forth below.
j. In paragraph (m)(2)(iv)(A)(1), by removing the citation
``319.40-7(f)'' and adding the citation ``part 305'' in its place.
k. 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.
l. 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]
37. Section 319.40-6 is amended as follows:
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.
b. In paragraphs (b)(1), (b)(1)(i), (b)(1)(ii), (b)(2)(ii),
(c)(2)(i)(B), (c)(2)(iii),
[[Page 22344]]
(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.
c. In paragraph (c)(1)(i)(A), by removing the citation ``Sec.
319.40-7(e)'' and adding the words ``part 305 of this chapter'' in its
place.
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.
38. Section 319.40-7 is amended as follows:
a. By removing paragraphs (c) through (f).
b. By adding a new paragraph (c) to read as set forth below.
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]
39. Section 319.41-5 is amended as follows:
a. In paragraph (a), by removing the words ``other necessary'' and
by adding the words ``in accordance with part 305 of this chapter,''
after the word ``treatment''.
b. 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]
40. Section 319.41-5a is removed.
Sec. 319.55-6 [Amended]
41. In Sec. 319.55-6, in paragraph (b)(1), the first sentence is
amended by adding the words ``in accordance with part 305 of this
chapter'' after the word ``treatment'' the first time it appears.
Sec. 319.56-3 [Amended]
42. 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]
43. 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]
44. 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]
45. Section 319.56-12 is amended by removing 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]
46. Section 319.56-13 is amended as follows:
a. In paragraph (b)(1)(ii), by removing the words ``an approved
treatment listed in''.
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]
47. In Sec. 319.56-21, paragraphs (b)(2) and (d)(2) are amended by
removing the words ``an approved treatment listed in''.
48. 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.
* * * * *
49. Section 319.56-23 is amended as follows:
a. In footnote 3, by removing the words ``a treatment listed in''.
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) * * *
(2) Treatments must be conducted in accordance with part 305 of
this chapter.
* * * * *
Sec. 319.56-38 [Amended]
50. 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]
51. 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]
52. Section 319.56-47, is amended as follows:
a. In paragraph (b) by removing the citation ``Sec. 305.31'' and
adding the words ``part 305'' in its place.
b. In paragraph (d) by removing the citation ``Sec. 305.31'' and
adding the words ``part 305 of this chapter'' in its place.
53. 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.
* * * * *
54. Section 319.74-2 is amended as follows:
a. In paragraph (c) by removing the paragraph designation (1)
following the heading ``Fumigation for agromyziads'' and removing
paragraph (c)(2).
b. Redesignating paragraphs (c)(1)(i) and (c)(1)(ii) as paragraphs
(c)(1) and (c)(2), respectively.
c. 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.
d. 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. * * *
* * * * *
[[Page 22345]]
PART 330--FEDERAL PLANT PEST REGULATIONS; GENERAL; PLANT PESTS;
SOIL, STONE, AND QUARRY PRODUCTS; GARBAGE
55. 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]
56. In Sec. 330.106, paragraph (a) the fourth sentence is amended
by adding the words ``in accordance with part 305 of this chapter''
after the word ``treatment.''
Sec. 330.300 [Amended]
57. 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
58. 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]
59. 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]
60. 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, this 28th day of April 2009.
Kevin Shea,
Acting Administrator, Animal and Plant Health Inspection Service.
[FR Doc. E9-10188 Filed 5-11-09; 8:45 am]
BILLING CODE 3410-34-P