National Poultry Improvement Plan and Auxiliary Provisions, 15791-15798 [2011-6539]
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15791
Rules and Regulations
Federal Register
Vol. 76, No. 55
Tuesday, March 22, 2011
This section of the FEDERAL REGISTER
contains regulatory documents having general
applicability and legal effect, most of which
are keyed to and codified in the Code of
Federal Regulations, which is published under
50 titles pursuant to 44 U.S.C. 1510.
The Code of Federal Regulations is sold by
the Superintendent of Documents. Prices of
new books are listed in the first FEDERAL
REGISTER issue of each week.
DEPARTMENT OF AGRICULTURE
Animal and Plant Health Inspection
Service
9 CFR Parts 56, 145, 146, and 147
[Docket No. APHIS–2009–0031]
RIN 0579–AD21
National Poultry Improvement Plan and
Auxiliary Provisions
Animal and Plant Health
Inspection Service, USDA.
ACTION: Final rule.
AGENCY:
We are amending the National
Poultry Improvement Plan (the Plan)
and its auxiliary provisions by
providing new or modified sampling
and testing procedures for Plan
participants and participating flocks.
The changes were voted on and
approved by the voting delegates at the
Plan’s 2008 National Plan Conference.
These changes will keep the provisions
of the Plan current with changes in the
poultry industry and provide for the use
of new sampling and testing procedures.
DATES: Effective Date: April 21, 2011.
FOR FURTHER INFORMATION CONTACT: Dr.
C. Stephen Roney, DVM, Senior Staff
Officer, NPIP, VS, APHIS, USDA, 1506
Klondike Road, Suite 300, Conyers, GA
30094–5104; (770) 922–3496.
SUPPLEMENTARY INFORMATION:
SUMMARY:
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Background
The National Poultry Improvement
Plan (NPIP, also referred to below as
‘‘the Plan’’) is a cooperative FederalState-industry mechanism for
controlling certain poultry diseases. The
Plan consists of a variety of programs
intended to prevent and control poultry
diseases. Participation in all Plan
programs is voluntary, but breeding
flocks, hatcheries, and dealers must first
qualify as ‘‘U.S. Pullorum-Typhoid
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Clean’’ as a condition for participating in
the other Plan programs.
The Plan identifies States, flocks,
hatcheries, dealers, and slaughter plants
that meet certain disease control
standards specified in the Plan’s various
programs. As a result, customers can
buy poultry that has tested clean of
certain diseases or that has been
produced under disease-prevention
conditions.
The regulations in 9 CFR parts 145,
146, and 147 (referred to below as the
regulations) contain the provisions of
the Plan. The Animal and Plant Health
Inspection Service (APHIS) of the U.S.
Department of Agriculture (USDA)
amends these provisions from time to
time to incorporate new scientific
information and technologies within the
Plan.
On September 20, 2010, we published
in the Federal Register (75 FR 57200–
57215, Docket No. APHIS–2009–0031) a
proposal 1 to amend the Plan and its
auxiliary provisions by providing new
or modified sampling and testing
procedures for Plan participants and
participating flocks. The proposed
changes were voted on and approved by
the voting delegates at the Plan’s 2008
National Plan Conference. These
changes were intended to keep the
provisions of the Plan current with
changes in the poultry industry and
provide for the use of new sampling and
testing procedures.
We solicited comments concerning
our proposal for 60 days ending
November 19, 2010. We received three
comments by that date. They were from
a producer and two citizens. One
commenter supported the proposed
rule, and one did not raise any issues
related to the proposed rule.
One commenter generally objected to
our proposed addition of provisions
under which a flock could be designated
‘‘Salmonella negative’’ to the regulations
in § 145.83(f) for the U.S. Salmonella
Monitored classification for primary
meat-type chicken breeding flocks.
However, this commenter did not raise
any specific concerns.
We continue to believe that the
Salmonella negative designation will
provide an effective means for flock
owners to demonstrate their flocks’
1 To view the proposed rule and the comments
we received, go to https://www.regulations.gov/
fdmspublic/component/main?main=DocketDetail&
d=APHIS-2009-0031.
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freedom from Salmonella based on
regular testing. We are not making any
changes to the proposed rule in
response to this comment.
We are, however, amending the
proposed provisions in paragraph (f) of
§ 145.83 to capitalize the word
Salmonella each time it is used.
In addition, our proposed changes to
paragraph (b) of § 145.14 indicated that
the polymerase chain reaction (PCR)based test is an official blood test for
Mycoplasma gallisepticum, M.
meleagridis, and M. synoviae. As the
PCR-based test is not a blood test, we
are changing proposed paragraph (b) to
refer simply to official tests.
Finally, we are updating the footnote
to the shoe cover sampling technique
we proposed to add in § 147.12 to give
the NPIP’s current address. It has
changed since the publication of the
proposal. We are also updating the
NPIP’s address in the other footnotes to
§ 147.12 and the footnote to § 147.5.
Therefore, for the reasons given in the
proposed rule and in this document, we
are adopting the proposed rule as a final
rule, with the changes discussed in this
document.
Executive Order 12866 and Regulatory
Flexibility Act
This final rule has been determined to
be not significant for the purposes of
Executive Order 12866 and, therefore,
has not been reviewed by the Office of
Management and Budget.
In accordance with the Regulatory
Flexibility Act, we have analyzed the
potential economic effects of this action
on small entities. The analysis is
summarized below. Copies of the full
analysis are available on the
Regulations.gov Web site (see footnote 1
in this document for a link to
Regulations.gov) or by contacting the
person listed under FOR FURTHER
INFORMATION CONTACT.
This rule will introduce a set of minor
changes to the NPIP and will not
involve significant changes in program
operations. These changes are in line
with the industry’s best practices and
would likely involve no additional costs
in order to meet these requirements.
Additionally, the NPIP is a voluntary
program established between the
industry and State and Federal
governments. Any person producing or
dealing in products may participate in
the NPIP when he or she has
demonstrated that his or her facilities,
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personnel, and practices are adequate
for carrying out the applicable
provisions of the NPIP. NPIP
participation allows for greater ease in
moving hatching eggs/live birds within
a State, across State lines, and into other
countries. Most countries will not
accept hatching eggs/live birds and
commercial poultry from a U.S.
operation unless it can be shown to be
a NPIP participant. The poultry industry
plays a very important role in the U.S.
economy, and these amendments will
help to ensure the safety of the industry
and benefit the economy.
Under these circumstances, the
Administrator of the Animal and Plant
Health Inspection Service has
determined that this action will not
have a significant economic impact on
a substantial number of small entities.
Executive Order 12372
This program/activity is listed in the
Catalog of Federal Domestic Assistance
under No. 10.025 and is subject to
Executive Order 12372, which requires
intergovernmental consultation with
State and local officials. (See 7 CFR part
3015, subpart V.)
Executive Order 12988
This final rule contains no new
information collection or recordkeeping
requirements under the Paperwork
Reduction Act of 1995 (44 U.S.C. 3501
et seq.).
List of Subjects
9 CFR Part 56
Animal diseases, Indemnity
payments, Low pathogenic avian
influenza, Poultry.
9 CFR Parts 145, 146, and 147
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Animal diseases, Poultry and poultry
products, Reporting and recordkeeping
requirements.
Accordingly, we are amending 9 CFR
parts 56, 145, 146, and 147 as follows:
Payment of indemnity.
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(b) * * *
(1) The poultry are from a breeding
flock that participates in any Plan
program in part 145 of this chapter but
that does not participate in the U.S.
Avian Influenza Clean or the U.S.
H5/H7 Avian Influenza Clean program
of the Plan available to the flock in part
145 of this chapter; or
(2) The poultry are from a commercial
flock or slaughter plant, but the flock or
slaughter plant does not participate in
the U.S. Avian Influenza Monitored
program available to the commercial
flock or slaughter plant in part 146 of
this chapter; or
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PART 145—NATIONAL POULTRY
IMPROVEMENT PLAN FOR BREEDING
POULTRY
4. The authority citation for part 145
continues to read as follows:
■
Authority: 7 U.S.C. 8301–8317; 7 CFR 2.22,
2.80, and 371.4.
5. Section 145.1 is amended by
adding, in alphabetical order, a new
definition of avian influenza to read as
follows:
1. The authority citation for 9 CFR
part 56 continues to read as follows:
■
§ 145.1
Authority: 7 U.S.C. 8301–8317; 7 CFR 2.22,
2.80, and 371.4.
2. Section 56.1 is amended as follows:
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Commercial flock or slaughter plant.
A commercial poultry flock or slaughter
plant that is required because of its size
to participate in the special provisions
in part 146 of this chapter in order to
participate in the Plan.
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■ 3. Section 56.3 is amended as follows:
■ a. In paragraph (b) introductory text,
by removing the word ‘‘(b)(7)’’ each time
it occurs and adding the word ‘‘(b)(3)’’ in
its place.
■ b. By revising paragraphs (b)(1) and
(b)(2) to read as set forth below.
■ c. By removing paragraphs (b)(4)
through (b)(6).
■ d. By redesignating paragraph (b)(7) as
paragraph (b)(3).
■
PART 56—CONTROL OF H5/H7 LOW
PATHOGENIC AVIAN INFLUENZA
16:40 Mar 21, 2011
Definitions.
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Paperwork Reduction Act
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§ 56.1
§ 56.3
This final rule has been reviewed
under Executive Order 12988, Civil
Justice Reform. This rule: (1) Has no
retroactive effect; and (2) does not
require administrative proceedings
before parties may file suit in court
challenging this rule.
■
a. By removing the definitions of
commercial meat-type flock,
commercial table-egg layer flock,
commercial table-egg layer premises,
meat-type chicken, and meat-type
turkey.
■ b. By adding a definition of
commercial flock or slaughter plant, in
alphabetical order, to read as set forth
below.
■
Definitions.
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Avian influenza. An infection or
disease of poultry caused by viruses in
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the family Orthomyxoviridae, genus
Influenzavirus A.
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■ 6. Section 145.10 is amended as
follows:
■ a. By revising the introductory text to
read as set forth below.
■ b. In paragraph (r), by removing the
words ‘‘and 145.53(e)’’ and adding the
words ‘‘145.63(b), 145.73(f), and
145.83(g)’’ in their place.
■ c. In paragraph (t), by removing the
citation ‘‘§ 145.43(g)’’ and adding the
words ‘‘§§ 145.43(g), 145.53(e), and
145.93(b)’’ in its place.
§ 145.10 Terminology and classification;
flocks, products, and States.
Participating flocks, products
produced from them, and States that
have met the requirements of a
classification in this part may be
designated by the corresponding
illustrative design in this section.
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■ 7. Section 145.14 is amended as
follows:
■ a. In the introductory text, in the first
sentence, by removing the word ‘‘blood’’
each time it occurs.
■ b. In the introductory text, in the
second sentence, by removing the words
‘‘Blood samples’’ and adding the word
‘‘Samples’’ in its place; and by removing
the word ‘‘drawn’’ and adding the word
‘‘collected’’ in its place.
■ c. By revising the heading of
paragraph (b) and paragraph (b)(1) to
read as set forth below.
■ d. In paragraph (b)(2), by adding the
word ‘‘serological’’ before the word
‘‘tests’’; and by adding the words ‘‘, M.
meleagridis,’’ after the word
‘‘gallisepticum’’.
■ e. By revising paragraph (b)(5) to read
as set forth below.
■ f. By removing and reserving
paragraph (c).
§ 145.14
Testing.
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(b) For Mycoplasma gallisepticum, M.
meleagridis, and M. synoviae. (1) The
official tests for M. gallisepticum, M.
meleagridis, and M. synoviae shall be
the serum plate agglutination test, the
tube agglutination test, the
hemagglutination inhibition (HI) test,
the microhemagglutination inhibition
test, the enzyme-linked immunosorbent
assay (ELISA) test,3 a polymerase chain
3 Procedures for the enzyme-linked
immunosorbent assay (ELISA) test are set forth in
the following publications:
A.A. Ansari, R.F. Taylor, T.S. Chang,
‘‘Application of Enzyme-Linked Immunosorbent
Assay for Detecting Antibody to Mycoplasma
gallisepticum Infections in Poultry,’’ Avian
Diseases, Vol. 27, No. 1, pp. 21–35, January–March
1983; and
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reaction (PCR)-based test, or a
combination of two or more of these
tests. The HI test or the
microhemagglutination inhibition test
shall be used to confirm the positive
results of other serological tests. HI
titers of 1:40 or more may be interpreted
as suspicious, and final judgment must
be based on further samplings and/or
culture of reactors.
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(5) The official molecular examination
procedures for M. gallisepticum are the
PCR test described in § 147.30 of this
subchapter and the real-time PCR test
described in § 147.31 of this subchapter.
The official molecular examination
procedure for M. synoviae is the PCR
test described in § 147.30 of this
subchapter.
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■ 8. Section 145.23 is amended as
follows:
■ a. In paragraph (b)(2)(iii), in the first
sentence, by removing the words ‘‘either
no poultry or’’, and by removing the
word ‘‘were’’ and adding the word ‘‘was’’
in its place.
■ b. In paragraph (h) introductory text,
by removing the words ‘‘serological’’ and
‘‘one of’’.
■ c. By adding a new paragraph (h)(1)
and revising paragraph (h)(2) to read as
set forth below.
§ 145.23 Terminology and classification;
flocks and products.
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(h) * * *
(1) It is a multiplier breeding flock in
which a minimum of 30 birds have been
tested negative for antibodies to avian
influenza when more than 4 months of
age. To retain this classification:
(i) A sample of at least 30 birds must
be tested negative at intervals of 90
days; or
(ii) A sample of fewer than 30 birds
may be tested, and found to be negative,
at any one time if all pens are equally
represented and a total of 30 birds is
tested within each 90-day period; or
(iii) The flock is tested as provided in
§ 145.14(d) at intervals of 30 days or less
and found to be negative, and a total of
30 samples are collected and tested
within each 90-day period; and
(2) During each 90-day period, all
multiplier spent fowl, up to a maximum
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*
H.M. Opitz, J.B. Duplessis, and M.J. Cyr, ‘‘Indirect
Micro-Enzyme-Linked Immunosorbent Assay for
the Detection of Antibodies to Mycoplasma
synoviae and M. gallisepticum,’’ Avian Diseases,
Vol. 27, No. 3, pp. 773–786, July–September 1983;
and
H.B. Ortmayer and R. Yamamoto, ‘‘Mycoplasma
Meleagridis Antibody Detection by Enzyme-Linked
Immunosorbent Assay (ELISA),’’ Proceedings, 30th
Western Poultry Disease Conference, pp. 63–66,
March 1981.
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of 30, must be tested and found negative
within 21 days prior to movement to
slaughter.
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§ 145.24
[Amended]
9. In § 145.24, paragraph (a)(1)(i) is
amended by removing the word ‘‘and’’
and by adding the words ‘‘, and
§ 145.93(b)(3)(i) through (vii)’’ before the
period at the end of the paragraph.
■ 10. Section 145.33 is amended as
follows:
■ a. In paragraph (b)(2)(iii), in the first
sentence, by removing the words ‘‘either
no poultry or’’, and by removing the
word ‘‘were’’ and adding the word ‘‘was’’
in its place.
■ b. In paragraph (l) introductory text,
by removing the words ‘‘serological’’ and
‘‘one of’’.
■ c. By adding a new paragraph (l)(1)
and revising paragraph (l)(2) to read as
set forth below.
■
§ 145.33 Terminology and classification;
flocks and products.
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(l) * * *
(1) It is a multiplier breeding flock in
which a minimum of 30 birds have been
tested negative for antibodies to avian
influenza when more than 4 months of
age. To retain this classification:
(i) A sample of at least 15 birds must
be tested negative at intervals of 90
days; or
(ii) A sample of fewer than 15 birds
may be tested, and found to be negative,
at any one time if all pens are equally
represented and a total of 30 birds is
tested within each 90-day period; or
(iii) The flock is tested as provided in
§ 145.14(d) at intervals of 30 days or less
and found to be negative, and a total of
15 samples are collected and tested
within each 90-day period; and
(2) During each 90-day period, all
multiplier spent fowl, up to a maximum
of 30, must be tested and found negative
within 21 days prior to movement to
slaughter.
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§ 145.34
[Amended]
11. In § 145.34, paragraph (a)(1)(i) is
amended by removing the word ‘‘and’’
and by adding the words ‘‘, and
§ 145.93(b)(3)(i) through (vii)’’ before the
period at the end of the paragraph.
■ 12. Section 145.43 is amended as
follows:
■ a. In paragraph (b)(2)(iii), in the first
sentence, by removing the words ‘‘either
no poultry or’’, and by removing the
word ‘‘were’’ and adding the word ‘‘was’’
in its place.
■ b. By removing and reserving
paragraphs (d)(2) and (d)(3).
■
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15793
c. In paragraph (f)(5), by redesignating
footnote 6 as footnote 5.
■ d. In paragraph (g) introductory text,
by removing the words ‘‘H5 and H7’’ and
adding the word ‘‘H5/H7’’ in their place
each time they appear; and by removing
the word ‘‘serological’’.
■ e. By revising paragraph (g)(1)
introductory text and paragraph (g)(2)
introductory text to read as set forth
below.
■ f. In paragraphs (g)(1)(i) and (g)(2)(i),
by removing the words ‘‘Provided, that
primary spent fowl be tested within 30
days prior to movement to disposal;’’.
■ g. By redesignating paragraph (g)(3) as
paragraph (g)(4).
■ h. By adding a new paragraph (g)(3) to
read as set forth below.
■
§ 145.43 Terminology and classification;
flocks and products.
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(g) * * *
(1) It is a primary breeding flock in
which a minimum of 30 birds have been
tested negative to the H5/H7 subtypes of
avian influenza as provided in
§ 145.14(d) when more than 4 months of
age and prior to the onset of egg
production. To retain this classification:
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(2) It is a multiplier breeding flock in
which a minimum of 30 birds have been
tested negative to the H5/H7 subtypes of
avian influenza as provided in
§ 145.14(d) when more than 4 months of
age and prior to the onset of egg
production. To retain this classification:
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(3) During each 90-day period, all
spent fowl, up to a maximum of 30,
must be tested and found negative
within 21 days prior to movement to
slaughter.
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§ 145.44
[Amended]
13. In § 145.44, paragraph (a)(1)(i) is
amended by removing the word ‘‘and’’;
and by adding the words ‘‘,
§ 145.73(b)(2)(i), § 145.83(b)(2)(i), and
§ 145.93(b)(3)(i) through (vii)’’ before the
period at the end of the paragraph.
■
Subpart E—Special Provisions for
Hobbyist and Exhibition Waterfowl,
Exhibition Poultry, and Game Bird
Breeding Flocks and Products
14. The heading for subpart E is
revised to read as set forth above.
■ 15. In § 145.52, the introductory text
is revised to read as follows:
■
§ 145.52
Participation.
Participating flocks of hobbyist and
exhibition waterfowl, exhibition
poultry, and game birds, and the eggs
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and baby poultry produced from them
shall comply with the applicable
general provisions of subpart A of this
part and the special provisions of this
subpart E. The special provisions that
apply to meat-type waterfowl flocks are
found in subpart I of this part.
■ 16. Section 145.53 is amended as
follows:
■ a. In paragraph (b)(2)(iii), in the first
sentence, by removing the words ‘‘either
no poultry or’’, and by removing the
word ‘‘were’’ and adding the word ‘‘was’’
in its place.
■ b. In paragraph (b)(5), by adding the
words ‘‘hobbyist or exhibition’’ before
the word ‘‘waterfowl’’.
■ c. In paragraph (e) in the introductory
text, second sentence, by adding the
words ‘‘hobbyist or exhibition’’ before
the word ‘‘waterfowl’’; and by removing
the word ‘‘serological’’.
■ d. In the introductory text of
paragraph (e)(1), by removing the words
‘‘for antibodies’’; and by removing the
words ‘‘by the agar gel immunodiffusion
test specified in § 147.9 of this chapter’’
and adding the words ‘‘as provided in
§ 145.14(d)’’ in their place.
■ e. In the introductory text of
paragraph (e)(2), by removing the words
‘‘for antibodies’’; and by removing the
words ‘‘by the agar gel immunodiffusion
test specified in § 147.9 of this chapter’’
and adding the words ‘‘as provided in
§ 145.14(d)’’ in their place.
■ f. By adding a new paragraph (e)(3) to
read as set forth below.
§ 145.53 Terminology and classification;
flocks and products.
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(e) * * *
(3) During each 90-day period, all
spent fowl, up to a maximum of 30,
must be tested and found negative
within 21 days prior to movement to
slaughter.
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§ 145.54
[Amended]
17. In § 145.54, paragraph (a)(1)(i) is
amended by removing the word ‘‘and’’;
and by adding the words ‘‘,
§ 145.73(b)(2)(i), § 145.83(b)(2)(i), and
§ 145.93(b)(3)(i) through (vii)’’ before the
period at the end of the paragraph.
■ 18. Section 145.73 is amended as
follows:
■ a. In the introductory text of
paragraph (f), second sentence, by
removing the word ‘‘serological.’’
■ b. By revising paragraph (f)(1) and
adding a new paragraph (f)(2) to read as
set forth below.
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■
§ 145.73 Terminology and classification;
flocks and products.
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(f) * * *
(1) It is a primary breeding flock in
which a minimum of 30 birds have been
tested negative for antibodies to avian
influenza when more than 4 months of
age. To retain this classification:
(i) A sample of at least 30 birds must
be tested negative at intervals of 90
days; or
(ii) A sample of fewer than 30 birds
may be tested, and found to be negative,
at any one time if all pens are equally
represented and a total of 30 birds is
tested within each 90-day period; or
(iii) The flock is tested as provided in
§ 145.14(d) at intervals of 30 days or less
and found to be negative, and a total of
30 samples are collected and tested
within each 90-day period; and
(2) During each 90-day period, all
primary spent fowl, up to a maximum
of 30, must be tested serologically and
found negative within 21 days prior to
movement to slaughter.
■ 19. Section 145.83 is amended as
follows:
■ a. In paragraph (f)(1)(vi), by removing
the semicolon at the end of the
paragraph and adding a period in its
place; and by adding a new sentence at
the end of the paragraph to read as set
forth below.
■ b. In paragraph (f)(1)(vii), by adding
the words ‘‘to allow for the serological
testing required under paragraph
(f)(1)(vi) of this section’’ after the word
‘‘age’’.
■ c. By adding a new paragraph
(f)(1)(viii) to read as set forth below.
■ d. In paragraph (f)(3), by removing the
words ‘‘this classification’’ and adding
the words ‘‘paragraphs (f)(1)(i) through
(f)(1)(vii) of this section’’ in their place.
■ e. In the introductory text of
paragraph (g), second sentence, by
removing the word ‘‘serological.’’
■ f. By revising paragraph (g)(1) and
adding a new paragraph (g)(2) to read as
set forth below.
§ 145.83 Terminology and classification;
flocks and products.
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(f) * * *
(1) * * *
(vi) * * * All Salmonella isolates
from a flock shall be serogrouped and
shall be reported to the Official State
Agency on a monthly basis;
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(viii) Any flock entering the
production period that is in compliance
with all the requirements of § 145.83(f)
with no history of Salmonella isolations
shall be considered ‘‘Salmonella
negative’’ and may retain this definition
as long as no environmental or bird
Salmonella isolations are identified and
confirmed from the flock or flock
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environment by sampling on 4 separate
collection dates over a minimum of a 2week period. Sampling and testing must
be performed as described in paragraph
(f)(1)(vi) of this section. An unconfirmed
environmental Salmonella isolation
shall not change this Salmonella
negative status.
*
*
*
*
*
(g) * * *
(1) It is a primary breeding flock in
which a minimum of 30 birds have been
tested negative for antibodies to avian
influenza when more than 4 months of
age. To retain this classification:
(i) A sample of at least 30 birds must
be tested negative at intervals of 90
days; or
(ii) A sample of fewer than 30 birds
may be tested, and found to be negative,
at any one time if all pens are equally
represented and a total of 30 birds is
tested within each 90-day period; or
(iii) The flock is tested as provided in
§ 145.14(d) at intervals of 30 days or less
and found to be negative, and a total of
30 samples are collected and tested
within each 90-day period; and
(2) During each 90-day period, all
primary spent fowl, up to a maximum
of 30, must be tested serologically and
found negative within 21 days prior to
movement to slaughter.
■ 20. A new subpart I, consisting of
§§ 145.91 through 145.94, is added to
read as follows:
Subpart I—Special Provisions for MeatType Waterfowl Breeding Flocks and
Products
Sec.
145.91 Definitions.
145.92 Participation.
145.93 Terminology and classification;
flocks and products.
145.94 Terminology and classification;
States.
Subpart I—Special Provisions for
Meat-Type Waterfowl Breeding Flocks
and Products
§ 145.91
Definitions.
Except where the context otherwise
requires, for the purposes of this subpart
the following term shall be construed to
mean:
Meat-type waterfowl breeding flocks.
Flocks of domesticated duck or goose
that are composed of stock that has been
developed and is maintained for the
primary purpose of producing baby
poultry that will be raised under
confinement for the primary purpose of
producing meat for human
consumption.
§ 145.92
Participation.
Participating flocks of meat-type
waterfowl and the eggs and baby poultry
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produced from them shall comply with
the applicable general provisions of
subpart A of this part and the special
provisions of this subpart I.
(a) Started poultry shall lose their
identity under Plan terminology when
not maintained by Plan participants
under the conditions prescribed in
§ 145.5(a).
(b) Hatching eggs produced by
primary breeding flocks shall be
fumigated (see § 147.25 of this chapter)
or otherwise sanitized.
(c) Any nutritive material provided to
baby poultry must be free of the avian
pathogens that are officially represented
in the Plan disease classifications listed
in § 145.10.
Emcdonald on DSK2BSOYB1PROD with RULES
§ 145.93 Terminology and classification;
flocks and products.
Participating flocks, and the eggs and
baby poultry produced from them, that
have met the respective requirements
specified in this section may be
designated by the following terms and
the corresponding designs illustrated in
§ 145.10.
(a) [Reserved]
(b) U.S. Pullorum-Typhoid Clean. A
flock in which freedom from pullorum
and typhoid has been demonstrated to
the Official State Agency under the
criteria in one of the following
paragraphs (b)(1) through (b)(5) of this
section (See § 145.14 relating to the
official blood test where applicable.):
(1) It has been officially blood tested
within the past 12 months with no
reactors.
(2) It is a multiplier breeding flock, or
a breeding flock composed of progeny of
a primary breeding flock which is
intended solely for the production of
multiplier breeding flocks, and meets
the following specifications as
determined by the Official State Agency
and the Service:
(i) The flock is located in a State
where all persons performing poultry
disease diagnostic services within the
State are required to report to the
Official State Agency within 48 hours
the source of all poultry specimens from
which S. pullorum or S. gallinarum is
isolated;
(ii) The flock is composed entirely of
birds that originated from U.S.
Pullorum-Typhoid Clean breeding
flocks or from flocks that met equivalent
requirements under official supervision;
and
(iii) The flock is located on a premises
where a flock not classified as U.S.
Pullorum-Typhoid Clean was located
the previous year; Provided, that an
Authorized Testing Agent must blood
test up to 300 birds per flock, as
described in § 145.14, if the Official
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State Agency determines that the flock
has been exposed to pullorum-typhoid.
In making determinations of exposure
and setting the number of birds to be
blood tested, the Official State Agency
shall evaluate the results of any blood
tests, described in § 145.14(a)(1), that
were performed on an unclassified flock
located on the premises during the
previous year; the origins of the
unclassified flock; and the probability of
contacts between the flock for which
qualification is being sought and
infected wild birds, contaminated feed
or waste, or birds, equipment, supplies,
or personnel from flocks infected with
pullorum-typhoid.
(3) It is a multiplier breeding flock
that originated from U.S. PullorumTyphoid Clean breeding flocks or from
flocks that met equivalent requirements
under official supervision, and is
located in a State in which it has been
determined by the Service that:
(i) All hatcheries within the State are
qualified as ‘‘National Plan Hatcheries’’
or have met equivalent requirements for
pullorum-typhoid control under official
supervision;
(ii) All hatchery supply flocks within
the State are qualified as U.S. PullorumTyphoid Clean or have met equivalent
requirements for pullorum-typhoid
control under official supervision:
Provided, That if other domesticated
fowl are maintained on the same
premises as the participating flock,
freedom from pullorum-typhoid
infection shall be demonstrated by an
official blood test of each of these fowl;
(iii) All shipments of products other
than U.S. Pullorum-Typhoid Clean, or
equivalent, into the State are prohibited;
(iv) All persons performing poultry
disease diagnostic services within the
State are required to report to the
Official State Agency within 48 hours
the source of all poultry specimens from
which S. pullorum or S. gallinarum is
isolated;
(v) All reports of any disease outbreak
involving a disease covered under the
Plan are promptly followed by an
investigation by the Official State
Agency to determine the origin of the
infection; Provided, That if the origin of
the infection involves another State, or
if there is exposure to poultry in another
State from the infected flock, then the
National Poultry Improvement Plan will
conduct an investigation;
(vi) All flocks found to be infected
with pullorum or typhoid are
quarantined until marketed or destroyed
under the supervision of the Official
State Agency, or until subsequently
blood tested, following the procedure
for reacting flocks as contained in
§ 145.14(a)(5), and all birds fail to
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demonstrate pullorum or typhoid
infection;
(vii) All poultry, including exhibition,
exotic, and game birds, but excluding
waterfowl, going to public exhibition
shall come from U.S. Pullorum-Typhoid
Clean or equivalent flocks, or have had
a negative pullorum-typhoid test within
90 days of going to public exhibition;
(viii) Discontinuation of any of the
conditions or procedures described in
paragraphs (a)(3)(i), (ii), (iii), (iv), (v),
(vi), and (vii) of this section, or the
occurrence of repeated outbreaks of
pullorum or typhoid in poultry breeding
flocks within or originating within the
State shall be grounds for the Service to
revoke its determination that such
conditions and procedures have been
met or complied with. Such action shall
not be taken until a thorough
investigation has been made by the
Service and the Official State Agency
has been given an opportunity to
present its views.
(4) It is a multiplier breeding flock
located in a State which has been
determined by the Service to be in
compliance with the provisions of
paragraph (a)(3) of this section, and in
which pullorum disease or fowl typhoid
is not known to exist nor to have existed
in hatchery supply flocks within the
State during the preceding 24 months.
(5) It is a primary breeding flock
located in a State determined to be in
compliance with the provisions of
paragraph (a)(4) of this section, and in
which a sample of 300 birds from flocks
of more than 300, and each bird in
flocks of 300 or less, has been officially
tested for pullorum-typhoid within the
past 12 months with no reactors:
Provided, That when a flock is a
primary breeding flock located in a State
which has been deemed to be a U.S.
Pullorum-Typhoid Clean State for the
past 3 years, and during which time no
isolation of pullorum or typhoid has
been made that can be traced to a source
in that State, a bacteriological
examination monitoring program or a
serological examination monitoring
program acceptable to the Official State
Agency and approved by the Service
may be used in lieu of annual blood
testing.
(c) U.S. H5/H7 Avian Influenza Clean.
This program is intended to be the basis
from which the breeding-hatchery
industry may conduct a program for the
prevention and control of the H5/H7
subtypes of avian influenza. It is
intended to determine the presence of
the H5/H7 subtypes of avian influenza
in meat-type waterfowl breeding flocks
through routine surveillance of each
participating breeding flock. A flock,
and the hatching eggs and baby poultry
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produced from it, will qualify for this
classification when the Official State
Agency determines that it has met one
of the following requirements:
(1) It is a primary breeding flock in
which a minimum of 30 birds have been
tested negative to the H5/H7 subtypes of
avian influenza as provided in
§ 145.14(d) when more than 4 months of
age. To retain this classification:
(i) A sample of at least 30 birds must
be tested and found to be negative at
intervals of 90 days; or
(ii) A sample of fewer than 30 birds
may be tested, and found to be negative,
at any one time if all pens are equally
represented and a total of 30 birds are
tested within each 90-day period.
(2) It is a multiplier breeding flock in
which a minimum of 30 birds have been
tested negative to the H5/H7 subtypes of
avian influenza as provided in
§ 145.14(d) when more than 4 months of
age. To retain this classification:
(i) A sample of at least 30 birds must
be tested negative at intervals of 180
days; or
(ii) A sample of fewer than 30 birds
may be tested, and found to be negative,
at any one time if all pens are equally
represented and a total of 30 birds are
tested within each 180-day period.
(3) During each 90-day period, all
spent fowl, up to a maximum of 30,
must be tested serologically and found
negative within 21 days prior to
movement to slaughter.
Emcdonald on DSK2BSOYB1PROD with RULES
§ 145.94
States.
Terminology and classification;
(a) U.S. Pullorum-Typhoid Clean
State. (1) A State will be declared a U.S.
Pullorum-Typhoid Clean State when it
has been determined by the Service that:
(i) The State is in compliance with the
provisions contained in
§§ 145.23(b)(3)(i) through (vii),
145.33(b)(3)(i) through (vii),
145.43(b)(3)(i) through (vi),
145.53(b)(3)(i) through (vii),
145.73(b)(2)(i), 145.83(b)(2)(i), and
145.93(b)(3)(i) through (vii).
(ii) No pullorum disease or fowl
typhoid is known to exist nor to have
existed in hatchery supply flocks within
the State during the preceding 12
months: Provided, That pullorum
disease or fowl typhoid found within
the preceding 24 months in waterfowl,
exhibition poultry, and game bird
breeding flocks will not prevent a State
that is otherwise eligible from
qualifying.
(2) Discontinuation of any of the
conditions described in paragraph
(a)(1)(i) of this section, or repeated
outbreaks of pullorum or typhoid occur
in hatchery supply flocks described in
paragraph (a)(1)(ii) of this section, or if
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an infection spreads from the
originating premises, the Service shall
have grounds to revoke its
determination that the State is entitled
to this classification. Such action shall
not be taken until a thorough
investigation has been made by the
Service and the Official State Agency
has been given an opportunity for a
hearing in accordance with rules of
practice adopted by the Administrator.
(b) [Reserved]
PART 146—NATIONAL POULTRY
IMPROVEMENT PLAN FOR
COMMERCIAL POULTRY
21. The authority citation for part 146
continues to read as follows:
■
Authority: 7 U.S.C. 8301–8317; 7 CFR 2.22,
2.80, and 371.4.
22. Section 146.1 is amended as
follows:
■ a. By revising the definitions of
commercial table-egg layer flock and
H5/H7 low pathogenic avian influenza
(LPAI) to read as set forth below.
■ b. By adding, in alphabetical order, a
new definition of commercial table-egg
layer pullet flock to read as set forth
below.
■
§ 146.1
Definitions.
*
*
*
*
*
Commercial table-egg layer flock. All
table-egg layers of common age or pullet
source on one premises.
*
*
*
*
*
Commercial table-egg layer pullet
flock. A table-egg layer flock prior to the
onset of egg production.
*
*
*
*
*
H5/H7 low pathogenic avian
influenza (LPAI). An infection of
poultry caused by an influenza A virus
of H5 or H7 subtype that has an
intravenous pathogenicity index in
6-week-old chickens less than 1.2 or less
than 75 percent mortality in 4- to
8-week-old chickens infected
intravenously, or an infection with
influenza A viruses of H5 or H7 subtype
with a cleavage site that is not
consistent with a previously identified
highly pathogenic avian influenza virus.
*
*
*
*
*
23. Section 146.9 is amended by
revising the introductory text to read as
follows:
■
§ 146.9 Terminology and classification;
flocks, products, and States.
Participating flocks, products
produced from them, and States that
have met the requirements of a
classification in this part may be
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designated by the corresponding
illustrative design in this section.
*
*
*
*
*
■ 24. Section 146.21 is amended by
adding a new definition of table-egg
layer pullet in alphabetical order to read
as follows:
§ 146.21
Definitions.
*
*
*
*
*
Table-egg layer pullet. A sexually
immature domesticated chicken grown
for the primary purpose of producing
eggs for human consumption.
■ 25. In § 146.23, paragraph (a) is
revised to read as follows:
§ 146.23 Terminology and classification;
flocks and products.
*
*
*
*
*
(a) U.S. H5/H7 Avian Influenza
Monitored. This program is intended to
be the basis from which the table-egg
layer industry may conduct a program
to monitor for the H5/H7 subtypes of
avian influenza. It is intended to
determine the presence of the H5/H7
subtypes of avian influenza in table-egg
layers and table-egg layer pullets
through routine surveillance of each
participating commercial table-egg layer
and table-egg layer pullet flock. A flock
will qualify for this classification when
the Official State Agency determines
that it has met one of the following
requirements:
(1) Table-egg layer pullet flocks. (i) It
is a commercial table-egg layer pullet
flock in which a minimum of 11 birds
have been tested negative to the H5/H7
subtypes of avian influenza as provided
in § 146.13(b) within 30 days prior to
movement; or
(ii) It is a commercial table-egg layer
pullet flock that has an ongoing active
and diagnostic surveillance program for
the H5/H7 subtypes of avian influenza
in which the number of birds tested is
equivalent to the number required in
paragraph (a)(1)(i) of this section and
that is approved by the Official State
Agency and the Service.
(2) Table-egg layer flocks. (i) It is a
commercial table-egg layer flock in
which a minimum of 11 birds have been
tested negative to the H5/H7 subtypes of
avian influenza as provided in
§ 146.13(b) within 30 days prior to
disposal;
(ii) It is a commercial table-egg layer
flock in which a minimum of 11 birds
have been tested negative for the H5/H7
subtypes of avian influenza as provided
in § 146.13(b) within a 12-month period;
or
(iii) It is a commercial table-egg layer
flock that has an ongoing active and
diagnostic surveillance program for the
H5/H7 subtypes of avian influenza in
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which the number of birds tested is
equivalent to the number required in
paragraph (a)(2)(i) or paragraph (a)(2)(ii)
of this section and that is approved by
the Official State Agency and the
Service.
*
*
*
*
*
§ 146.24
[Amended]
26. Section 146.24 is amended as
follows:
■ a. In paragraph (a)(1)(i), by adding the
words ‘‘and all commercial table-egg
layer pullet flocks that supply those
flocks’’ after the word ‘‘flocks’’.
■ b. In paragraphs (a)(1)(iii) through
(a)(1)(v), by adding the words ‘‘and
table-egg layer pullet’’ after the word
‘‘layer’’ each time it occurs.
■
§ 146.33
[Amended]
27. In § 146.33, paragraphs (a)(1) and
(a)(2) are amended by adding the words
‘‘, as provided in § 146.13(b),’’ after the
word ‘‘influenza,’’ each time it occurs.
■
§ 146.43
[Amended]
28. In § 146.43, paragraph (a)(1) is
amended by adding the words ‘‘, as
provided in § 146.13(b),’’ after the word
‘‘influenza’’ and by removing the word
‘‘virus’’.
■
§ 146.53
[Amended]
29. Section 146.53 is amended as
follows:
■ a. In paragraph (a)(1), by adding the
words ‘‘, as provided in § 146.13(b),’’
after the word ‘‘influenza.’’
■ b. In paragraph (a)(2), by removing the
words ‘‘antibodies to’’ and by adding the
words ‘‘, as provided in § 146.13(b),’’
after the word ‘‘influenza.’’
■ c. In paragraph (b), in the last
sentence, by adding the words ‘‘, as
provided in § 146.13(b),’’ after the word
‘‘influenza.’’
■
PART 147—AUXILIARY PROVISIONS
ON NATIONAL POULTRY
IMPROVEMENT PLAN
30. The authority citation for part 147
continues to read as follows:
■
Authority: 7 U.S.C. 8301–8317; 7 CFR 2.22,
2.80, and 371.4.
§ 147.5
[Amended]
31. In § 147.5, footnote 4 to paragraph
(b) is amended by removing the words
‘‘1498 Klondike Road, Suite 200’’ and
adding the words ‘‘1506 Klondike Road,
Suite 300’’ in their place.
■ 32. Section 147.6 is amended as
follows:
■ a. By revising the introductory text
and paragraphs (a)(1) through (a)(4) to
read as set forth below.
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■
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b. By removing paragraphs (a)(5)
through (a)(15).
■
§ 147.6 Procedures for determining the
status of flocks reacting to test for
Mycoplasma gallisepticum, Mycoplasma
synoviae, and Mycoplasma melagridis.
Procedures for isolation and
identification of Mycoplasma may be
found in Isolation and Identification of
Avian Pathogens, published by the
American Association of Avian
Pathologists; Kleven, S.H., F.T.W.
Jordan, and J.M. Bradbury, Avian
Mycoplasmosis (Mycoplasma
gallisepticum), Manual of Diagnostic
Tests and Vaccines for Terrestrial
Animals, Fifth Ed., Office International
des Epizooties, pp 842–855, 2004; and
§§ 147.15 and 147.16.
(a) * * *
(1) If the tube agglutination test,
enzyme-labeled immunosorbent assay
(ELISA), official molecular examination
procedure, or serum plate test is
negative, the flock qualifies for the
classification for which it was tested.
(2) If the tube agglutination, ELISA, or
serum plate test is positive, the
hemaglutination inhibition (HI) test or a
molecular examination procedure shall
be conducted: Provided, for the HI test,
that if more than 50 percent of the
samples are positive for M.
gallisepticum, M. meleagridis, or M.
synoviae, the HI test shall be conducted
on 10 percent of the positive samples or
25 positive samples, whichever is
greater. HI titers of 1:40 or more may be
interpreted as suspicious and
appropriate antigen detection samples
should be taken promptly (within 7
days of the original sampling) from 30
clinically affected birds and examined
by an approved cultural technique
individually, or pooled (up to 5 swabs
per test) and used in a molecular
examination procedure or in vivo
bioassay.
(3) If the in vivo bioassay, molecular
examination procedure, or culture
procedure is negative, the Official State
Agency may qualify the flock for the
classification for which it was tested. In
the event of contaminated cultures, the
molecular examination technique must
be used to make a final determination.
(4) If the in vivo bioassay, molecular
examination procedure, or culture
procedure is positive, the flock will be
considered infected.
*
*
*
*
*
§§ 147.12, 147.14, 147.15, 147.16, 147.30,
and 147.31 [Amended]
33. In §§ 147.12, 147.14, 147.15,
147.16, 147.30, and 147.31, footnotes 9
through 21 are redesignated as footnotes
10 through 22, respectively.
■
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15797
34. Section 147.12 is amended as
follows:
■ a. In footnote 8 to paragraph (a)(3), by
removing the words ‘‘1498 Klondike
Road, Suite 200’’ and adding the words
‘‘1506 Klondike Road, Suite 300’’ in
their place.
■ b. By adding a new paragraph (a)(6)
and a new footnote 9 to read as set forth
below.
■ c. In newly redesignated footnote 10
to paragraph (c)(3)(ii)(A), by removing
the words ‘‘1498 Klondike Road, Suite
200’’ and adding the words ‘‘1506
Klondike Road, Suite 300’’ in their
place.
■
§ 147.12 Procedures for collection,
isolation, and identification of Salmonella
from environmental samples, cloacal
swabs, chick box papers, and meconium
samples.
*
*
*
*
*
(a) * * *
(6) Shoe cover sampling technique.
Absorbable fabric shoe covers involve
the exposure of the bottom surface of
shoe covers to the surface of floor litter
and slat areas. Wearing clean latex
gloves, place the shoe covers over
footwear that is only worn inside the
poultry house. This can be footwear
dedicated to the facility or disposable
overshoes. Each pair of shoe covers
should be worn while walking at a
normal pace over a distance of 305
meters (1,000 feet). For flocks with
fewer than 500 breeders, at least 1 pair
of shoe covers should be worn to sample
the floor of the bird area. For flocks with
500 or more breeders, at least 2 pairs of
shoe covers should be worn to sample
the floor of the bird area. After
sampling, place each shoe cover in a
sterile container with 30 ml of double
strength skim milk.9 Seal the sterile
containers and promptly refrigerate
them at 2 to 4 °C or place in a cooler
with ice or ice packs. Do not freeze.
Samples should be stored at refrigerator
temperatures of 2 to 4 °C no more than
5 days prior to culturing.
*
*
*
*
*
■ 35. In § 147.45, the first sentence is
revised to read as follows:
§ 147.45
Official delegates.
Each cooperating State shall be
entitled to one official delegate for each
of the programs prescribed in parts 145
and 146 of this chapter in which it has
one or more participants at the time of
the Conference. * * *
9 Obtain procedure for preparing double strength
skim milk from USDA–APHIS ‘‘Recommended
Sample Collection Methods for Environmental
Samples,’’ available from the National Poultry
Improvement Plan, Veterinary Services, APHIS,
USDA, 1506 Klondike Road, Suite 300, Conyers, GA
30094.
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36. In § 147.52, a new paragraph (c) is
added to read as follows:
■
Background
*
*
*
*
(c) The following diagnostic test kits
that are not licensed by the Service (e.g.,
bacteriological culturing kits) are
approved for use in the NPIP:
(1) Rapid Chek©Select TMSalmonella
Test Kit, Strategic Diagnostics, Inc.,
Newark, DE 19713.
(2) ADIAFOOD Rapid Pathogen
Detection System for Salmonella spp.,
AES Chemunex Canada. Laval, QC
(Canada) H7L4S3.
(3) DuPont Qualicon BAX Polymerase
Chain Reaction (PCR)-based assay for
Salmonella, DuPont Qualicon,
Wilmington, DE 19810.
Done in Washington, DC, this 16th day of
March 2011.
Kevin Shea,
Acting Administrator, Animal and Plant
Health Inspection Service.
On March 2, 2007, Jet Aviation
Engineering Services L.P. (JAES), of
Teterboro, New Jersey, applied for a
supplemental type certificate for a
reconfiguration of an aircraft interior in
a 747–468. The Boeing Model 747–468
airplane is FAA approved under Type
Certificate A20WE as a large transportcategory airplane that is limited to 660
passengers or fewer, depending on the
interior configuration.
This modification includes the
installation of a medical lift between the
main deck and upper deck. The lift
allows the transport of a single occupant
between the decks during cruise or
ramp operations. The applicable
airworthiness regulations do not contain
adequate or appropriate safety standards
for this design feature.
Type Certification Basis
§ 147.52
Approved tests.
*
[FR Doc. 2011–6539 Filed 3–21–11; 8:45 am]
BILLING CODE 3410–34–P
DEPARTMENT OF TRANSPORTATION
Federal Aviation Administration
14 CFR Part 25
[Docket No. NM428; Special Condition No.
25–417–SC]
Special Conditions: Boeing 747–468,
Installation of a Medical Lift
Federal Aviation
Administration (FAA), DOT.
ACTION: Final special conditions.
AGENCY:
These special conditions are
issued for the Boeing 747–468 airplane.
This airplane, as modified by Jet
Aviation, will have a novel or unusual
design feature associated with the
installation of a medical lift. The
applicable airworthiness regulations do
not contain adequate or appropriate
safety standards for this design feature.
These special conditions contain the
additional safety standards that the
Administrator considers necessary to
establish a level of safety equivalent to
that established by the existing
airworthiness standards.
DATES: Effective Date: March 22, 2011.
FOR FURTHER INFORMATION CONTACT:
Jayson Claar, Transport Airplane
Directorate, Aircraft Certification
Service, 1601 Lind Avenue, SW.,
Renton, Washington 98057–3356;
telephone (425) 227–2194; fax (425)
227–1149; e-mail jayson.claar@faa.gov.
SUPPLEMENTARY INFORMATION:
Emcdonald on DSK2BSOYB1PROD with RULES
SUMMARY:
VerDate Mar<15>2010
16:40 Mar 21, 2011
Jkt 223001
Under the provisions of Title 14, Code
of Federal Regulations (14 CFR) 21.101,
JAES must show that the 747–468, as
changed, continues to meet the
applicable provisions of the regulations
incorporated by reference in Type
Certificate A20WE, or of the applicable
regulations in effect on the date of
application for the change. The
regulations incorporated by reference in
the type certificate are commonly
referred to as the ‘‘original typecertification basis.’’ The regulations
incorporated by reference in Type
Certificate A20WE are as follows:
• Part 36, as amended by
Amendments 36–1 through 36–15, and
any later amendments in existence at
the time of certification.
• Special Federal Aviation Regulation
(SFAR) 27, as amended by Amendments
27–1 through 27–6 and any later
amendments in existence at the time of
type certification.
• Part 25, effective February 1, 1965,
as amended by Amendments 25–1
through 25–59, and the part 25 sectionnumber exceptions itemized in Type
Certificate A20WE.
The following special conditions,
exemptions, and equivalent safety
findings, which are part of the Model
747–300 certification basis, are also part
of the certification basis for the Model
747–400.
The special conditions include those
enclosed with an FAA letter to The
Boeing Company dated February 20,
1970, and the following:
1. Special Condition 4A, revised to
apply to airplanes with the landing-gear
load-evener system deleted, was
recorded as an enclosure to an FAA
letter to The Boeing Company dated
May 12, 1971.
PO 00000
Frm 00008
Fmt 4700
Sfmt 4700
2. Special Condition No. 25–61–NW–
1, for occupancy not to exceed 32
passengers on the upper deck of
airplanes with a spiral staircase, was
transmitted to The Boeing Company by
FAA letter dated February 26, 1975.
3. Special Condition No. 25–71–NW–
3, for occupancy not to exceed 45
passengers on the upper deck of
airplanes with a straight-segmented
stairway, was transmitted to The Boeing
Company by FAA letter dated
September 8, 1976.
4. Modification of Special Condition
No. 25–71–NW–3, for occupancy not to
exceed 110 passengers on the upper
deck of airplanes with a straightsegmented stairway, was transmitted to
The Boeing Company by FAA letter
dated August 3, 1981.
5. Special Condition No. 25–77–NW–
4, modification of the autopilot system
to approve the airplane for use of the
system under Category IIIb landing
conditions, was transmitted to The
Boeing Company by FAA letter dated
July 8, 1977.
6. Special Condition No. 25–ANM–16,
for use of an overhead crew-rest area,
occupancy not to exceed ten
crewmembers, was transmitted to The
Boeing Company by FAA letter dated
November 19, 1987. The FAA-approved
procedures required for compliance
with paragraph 13 of the special
condition are located in Boeing
Document D926U303, Appendix D.
7. Special Condition no. 25–ANM–24,
applicable to flight-deck displays and
propulsion-control systems, was
provided to Boeing on December 22,
1988.
8. Special Condition No. 25–ANM–25,
which established lightning- and radiofrequency-energy protection
requirements, was provided to Boeing
on December 22, 1988.
Exemptions From Part 25
Exemption no. 1013A, dated
December 24, 1969: Exemption from
Section 25.471(b) to allow lateral
displacement of the center of gravity
from the airplane centerline.
The following optional requirements,
which are part of the Model 747–300
certification basis, apply also to the
747–400:
TABLE 1—OPTIONAL REQUIREMENTS
Requirement
Ditching provisions .............
Ice-protection provisions .....
Section
25.801
25.1419
The following equivalent-safety
findings, previously made for earlier
models under the provisions of
E:\FR\FM\22MRR1.SGM
22MRR1
Agencies
[Federal Register Volume 76, Number 55 (Tuesday, March 22, 2011)]
[Rules and Regulations]
[Pages 15791-15798]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2011-6539]
========================================================================
Rules and Regulations
Federal Register
________________________________________________________________________
This section of the FEDERAL REGISTER contains regulatory documents
having general applicability and legal effect, most of which are keyed
to and codified in the Code of Federal Regulations, which is published
under 50 titles pursuant to 44 U.S.C. 1510.
The Code of Federal Regulations is sold by the Superintendent of Documents.
Prices of new books are listed in the first FEDERAL REGISTER issue of each
week.
========================================================================
Federal Register / Vol. 76, No. 55 / Tuesday, March 22, 2011 / Rules
and Regulations
[[Page 15791]]
DEPARTMENT OF AGRICULTURE
Animal and Plant Health Inspection Service
9 CFR Parts 56, 145, 146, and 147
[Docket No. APHIS-2009-0031]
RIN 0579-AD21
National Poultry Improvement Plan and Auxiliary Provisions
AGENCY: Animal and Plant Health Inspection Service, USDA.
ACTION: Final rule.
-----------------------------------------------------------------------
SUMMARY: We are amending the National Poultry Improvement Plan (the
Plan) and its auxiliary provisions by providing new or modified
sampling and testing procedures for Plan participants and participating
flocks. The changes were voted on and approved by the voting delegates
at the Plan's 2008 National Plan Conference. These changes will keep
the provisions of the Plan current with changes in the poultry industry
and provide for the use of new sampling and testing procedures.
DATES: Effective Date: April 21, 2011.
FOR FURTHER INFORMATION CONTACT: Dr. C. Stephen Roney, DVM, Senior
Staff Officer, NPIP, VS, APHIS, USDA, 1506 Klondike Road, Suite 300,
Conyers, GA 30094-5104; (770) 922-3496.
SUPPLEMENTARY INFORMATION:
Background
The National Poultry Improvement Plan (NPIP, also referred to below
as ``the Plan'') is a cooperative Federal-State-industry mechanism for
controlling certain poultry diseases. The Plan consists of a variety of
programs intended to prevent and control poultry diseases.
Participation in all Plan programs is voluntary, but breeding flocks,
hatcheries, and dealers must first qualify as ``U.S. Pullorum-Typhoid
Clean'' as a condition for participating in the other Plan programs.
The Plan identifies States, flocks, hatcheries, dealers, and
slaughter plants that meet certain disease control standards specified
in the Plan's various programs. As a result, customers can buy poultry
that has tested clean of certain diseases or that has been produced
under disease-prevention conditions.
The regulations in 9 CFR parts 145, 146, and 147 (referred to below
as the regulations) contain the provisions of the Plan. The Animal and
Plant Health Inspection Service (APHIS) of the U.S. Department of
Agriculture (USDA) amends these provisions from time to time to
incorporate new scientific information and technologies within the
Plan.
On September 20, 2010, we published in the Federal Register (75 FR
57200-57215, Docket No. APHIS-2009-0031) a proposal \1\ to amend the
Plan and its auxiliary provisions by providing new or modified sampling
and testing procedures for Plan participants and participating flocks.
The proposed changes were voted on and approved by the voting delegates
at the Plan's 2008 National Plan Conference. These changes were
intended to keep the provisions of the Plan current with changes in the
poultry industry and provide for the use of new sampling and testing
procedures.
---------------------------------------------------------------------------
\1\ To view the proposed rule and the comments we received, go
to https://www.regulations.gov/fdmspublic/component/main?main=DocketDetail&d=APHIS-2009-0031.
---------------------------------------------------------------------------
We solicited comments concerning our proposal for 60 days ending
November 19, 2010. We received three comments by that date. They were
from a producer and two citizens. One commenter supported the proposed
rule, and one did not raise any issues related to the proposed rule.
One commenter generally objected to our proposed addition of
provisions under which a flock could be designated ``Salmonella
negative'' to the regulations in Sec. 145.83(f) for the U.S.
Salmonella Monitored classification for primary meat-type chicken
breeding flocks. However, this commenter did not raise any specific
concerns.
We continue to believe that the Salmonella negative designation
will provide an effective means for flock owners to demonstrate their
flocks' freedom from Salmonella based on regular testing. We are not
making any changes to the proposed rule in response to this comment.
We are, however, amending the proposed provisions in paragraph (f)
of Sec. 145.83 to capitalize the word Salmonella each time it is used.
In addition, our proposed changes to paragraph (b) of Sec. 145.14
indicated that the polymerase chain reaction (PCR)-based test is an
official blood test for Mycoplasma gallisepticum, M. meleagridis, and
M. synoviae. As the PCR-based test is not a blood test, we are changing
proposed paragraph (b) to refer simply to official tests.
Finally, we are updating the footnote to the shoe cover sampling
technique we proposed to add in Sec. 147.12 to give the NPIP's current
address. It has changed since the publication of the proposal. We are
also updating the NPIP's address in the other footnotes to Sec. 147.12
and the footnote to Sec. 147.5.
Therefore, for the reasons given in the proposed rule and in this
document, we are adopting the proposed rule as a final rule, with the
changes discussed in this document.
Executive Order 12866 and Regulatory Flexibility Act
This final rule has been determined to be not significant for the
purposes of Executive Order 12866 and, therefore, has not been reviewed
by the Office of Management and Budget.
In accordance with the Regulatory Flexibility Act, we have analyzed
the potential economic effects of this action on small entities. The
analysis is summarized below. Copies of the full analysis are available
on the Regulations.gov Web site (see footnote 1 in this document for a
link to Regulations.gov) or by contacting the person listed under FOR
FURTHER INFORMATION CONTACT.
This rule will introduce a set of minor changes to the NPIP and
will not involve significant changes in program operations. These
changes are in line with the industry's best practices and would likely
involve no additional costs in order to meet these requirements.
Additionally, the NPIP is a voluntary program established between the
industry and State and Federal governments. Any person producing or
dealing in products may participate in the NPIP when he or she has
demonstrated that his or her facilities,
[[Page 15792]]
personnel, and practices are adequate for carrying out the applicable
provisions of the NPIP. NPIP participation allows for greater ease in
moving hatching eggs/live birds within a State, across State lines, and
into other countries. Most countries will not accept hatching eggs/live
birds and commercial poultry from a U.S. operation unless it can be
shown to be a NPIP participant. The poultry industry plays a very
important role in the U.S. economy, and these amendments will help to
ensure the safety of the industry and benefit the economy.
Under these circumstances, the Administrator of the Animal and
Plant Health Inspection Service has determined that this action will
not have a significant economic impact on a substantial number of small
entities.
Executive Order 12372
This program/activity is listed in the Catalog of Federal Domestic
Assistance under No. 10.025 and is subject to Executive Order 12372,
which requires intergovernmental consultation with State and local
officials. (See 7 CFR part 3015, subpart V.)
Executive Order 12988
This final rule has been reviewed under Executive Order 12988,
Civil Justice Reform. This rule: (1) Has no retroactive effect; and (2)
does not require administrative proceedings before parties may file
suit in court challenging this rule.
Paperwork Reduction Act
This final rule contains no new information collection or
recordkeeping requirements under the Paperwork Reduction Act of 1995
(44 U.S.C. 3501 et seq.).
List of Subjects
9 CFR Part 56
Animal diseases, Indemnity payments, Low pathogenic avian
influenza, Poultry.
9 CFR Parts 145, 146, and 147
Animal diseases, Poultry and poultry products, Reporting and
recordkeeping requirements.
Accordingly, we are amending 9 CFR parts 56, 145, 146, and 147 as
follows:
PART 56--CONTROL OF H5/H7 LOW PATHOGENIC AVIAN INFLUENZA
0
1. The authority citation for 9 CFR part 56 continues to read as
follows:
Authority: 7 U.S.C. 8301-8317; 7 CFR 2.22, 2.80, and 371.4.
0
2. Section 56.1 is amended as follows:
0
a. By removing the definitions of commercial meat-type flock,
commercial table-egg layer flock, commercial table-egg layer premises,
meat-type chicken, and meat-type turkey.
0
b. By adding a definition of commercial flock or slaughter plant, in
alphabetical order, to read as set forth below.
Sec. 56.1 Definitions.
* * * * *
Commercial flock or slaughter plant. A commercial poultry flock or
slaughter plant that is required because of its size to participate in
the special provisions in part 146 of this chapter in order to
participate in the Plan.
* * * * *
0
3. Section 56.3 is amended as follows:
0
a. In paragraph (b) introductory text, by removing the word ``(b)(7)''
each time it occurs and adding the word ``(b)(3)'' in its place.
0
b. By revising paragraphs (b)(1) and (b)(2) to read as set forth below.
0
c. By removing paragraphs (b)(4) through (b)(6).
0
d. By redesignating paragraph (b)(7) as paragraph (b)(3).
Sec. 56.3 Payment of indemnity.
* * * * *
(b) * * *
(1) The poultry are from a breeding flock that participates in any
Plan program in part 145 of this chapter but that does not participate
in the U.S. Avian Influenza Clean or the U.S. H5/H7 Avian Influenza
Clean program of the Plan available to the flock in part 145 of this
chapter; or
(2) The poultry are from a commercial flock or slaughter plant, but
the flock or slaughter plant does not participate in the U.S. Avian
Influenza Monitored program available to the commercial flock or
slaughter plant in part 146 of this chapter; or
* * * * *
PART 145--NATIONAL POULTRY IMPROVEMENT PLAN FOR BREEDING POULTRY
0
4. The authority citation for part 145 continues to read as follows:
Authority: 7 U.S.C. 8301-8317; 7 CFR 2.22, 2.80, and 371.4.
0
5. Section 145.1 is amended by adding, in alphabetical order, a new
definition of avian influenza to read as follows:
Sec. 145.1 Definitions.
* * * * *
Avian influenza. An infection or disease of poultry caused by
viruses in the family Orthomyxoviridae, genus Influenzavirus A.
* * * * *
0
6. Section 145.10 is amended as follows:
0
a. By revising the introductory text to read as set forth below.
0
b. In paragraph (r), by removing the words ``and 145.53(e)'' and adding
the words ``145.63(b), 145.73(f), and 145.83(g)'' in their place.
0
c. In paragraph (t), by removing the citation ``Sec. 145.43(g)'' and
adding the words ``Sec. Sec. 145.43(g), 145.53(e), and 145.93(b)'' in
its place.
Sec. 145.10 Terminology and classification; flocks, products, and
States.
Participating flocks, products produced from them, and States that
have met the requirements of a classification in this part may be
designated by the corresponding illustrative design in this section.
* * * * *
0
7. Section 145.14 is amended as follows:
0
a. In the introductory text, in the first sentence, by removing the
word ``blood'' each time it occurs.
0
b. In the introductory text, in the second sentence, by removing the
words ``Blood samples'' and adding the word ``Samples'' in its place;
and by removing the word ``drawn'' and adding the word ``collected'' in
its place.
0
c. By revising the heading of paragraph (b) and paragraph (b)(1) to
read as set forth below.
0
d. In paragraph (b)(2), by adding the word ``serological'' before the
word ``tests''; and by adding the words ``, M. meleagridis,'' after the
word ``gallisepticum''.
0
e. By revising paragraph (b)(5) to read as set forth below.
0
f. By removing and reserving paragraph (c).
Sec. 145.14 Testing.
* * * * *
(b) For Mycoplasma gallisepticum, M. meleagridis, and M. synoviae.
(1) The official tests for M. gallisepticum, M. meleagridis, and M.
synoviae shall be the serum plate agglutination test, the tube
agglutination test, the hemagglutination inhibition (HI) test, the
microhemagglutination inhibition test, the enzyme-linked immunosorbent
assay (ELISA) test,\3\ a polymerase chain
[[Page 15793]]
reaction (PCR)-based test, or a combination of two or more of these
tests. The HI test or the microhemagglutination inhibition test shall
be used to confirm the positive results of other serological tests. HI
titers of 1:40 or more may be interpreted as suspicious, and final
judgment must be based on further samplings and/or culture of reactors.
---------------------------------------------------------------------------
\3\ Procedures for the enzyme-linked immunosorbent assay (ELISA)
test are set forth in the following publications:
A.A. Ansari, R.F. Taylor, T.S. Chang, ``Application of Enzyme-
Linked Immunosorbent Assay for Detecting Antibody to Mycoplasma
gallisepticum Infections in Poultry,'' Avian Diseases, Vol. 27, No.
1, pp. 21-35, January-March 1983; and
H.M. Opitz, J.B. Duplessis, and M.J. Cyr, ``Indirect Micro-
Enzyme-Linked Immunosorbent Assay for the Detection of Antibodies to
Mycoplasma synoviae and M. gallisepticum,'' Avian Diseases, Vol. 27,
No. 3, pp. 773-786, July-September 1983; and
H.B. Ortmayer and R. Yamamoto, ``Mycoplasma Meleagridis Antibody
Detection by Enzyme-Linked Immunosorbent Assay (ELISA),''
Proceedings, 30th Western Poultry Disease Conference, pp. 63-66,
March 1981.
---------------------------------------------------------------------------
* * * * *
(5) The official molecular examination procedures for M.
gallisepticum are the PCR test described in Sec. 147.30 of this
subchapter and the real-time PCR test described in Sec. 147.31 of this
subchapter. The official molecular examination procedure for M.
synoviae is the PCR test described in Sec. 147.30 of this subchapter.
* * * * *
0
8. Section 145.23 is amended as follows:
0
a. In paragraph (b)(2)(iii), in the first sentence, by removing the
words ``either no poultry or'', and by removing the word ``were'' and
adding the word ``was'' in its place.
0
b. In paragraph (h) introductory text, by removing the words
``serological'' and ``one of''.
0
c. By adding a new paragraph (h)(1) and revising paragraph (h)(2) to
read as set forth below.
Sec. 145.23 Terminology and classification; flocks and products.
* * * * *
(h) * * *
(1) It is a multiplier breeding flock in which a minimum of 30
birds have been tested negative for antibodies to avian influenza when
more than 4 months of age. To retain this classification:
(i) A sample of at least 30 birds must be tested negative at
intervals of 90 days; or
(ii) A sample of fewer than 30 birds may be tested, and found to be
negative, at any one time if all pens are equally represented and a
total of 30 birds is tested within each 90-day period; or
(iii) The flock is tested as provided in Sec. 145.14(d) at
intervals of 30 days or less and found to be negative, and a total of
30 samples are collected and tested within each 90-day period; and
(2) During each 90-day period, all multiplier spent fowl, up to a
maximum of 30, must be tested and found negative within 21 days prior
to movement to slaughter.
* * * * *
Sec. 145.24 [Amended]
0
9. In Sec. 145.24, paragraph (a)(1)(i) is amended by removing the word
``and'' and by adding the words ``, and Sec. 145.93(b)(3)(i) through
(vii)'' before the period at the end of the paragraph.
0
10. Section 145.33 is amended as follows:
0
a. In paragraph (b)(2)(iii), in the first sentence, by removing the
words ``either no poultry or'', and by removing the word ``were'' and
adding the word ``was'' in its place.
0
b. In paragraph (l) introductory text, by removing the words
``serological'' and ``one of''.
0
c. By adding a new paragraph (l)(1) and revising paragraph (l)(2) to
read as set forth below.
Sec. 145.33 Terminology and classification; flocks and products.
* * * * *
(l) * * *
(1) It is a multiplier breeding flock in which a minimum of 30
birds have been tested negative for antibodies to avian influenza when
more than 4 months of age. To retain this classification:
(i) A sample of at least 15 birds must be tested negative at
intervals of 90 days; or
(ii) A sample of fewer than 15 birds may be tested, and found to be
negative, at any one time if all pens are equally represented and a
total of 30 birds is tested within each 90-day period; or
(iii) The flock is tested as provided in Sec. 145.14(d) at
intervals of 30 days or less and found to be negative, and a total of
15 samples are collected and tested within each 90-day period; and
(2) During each 90-day period, all multiplier spent fowl, up to a
maximum of 30, must be tested and found negative within 21 days prior
to movement to slaughter.
* * * * *
Sec. 145.34 [Amended]
0
11. In Sec. 145.34, paragraph (a)(1)(i) is amended by removing the
word ``and'' and by adding the words ``, and Sec. 145.93(b)(3)(i)
through (vii)'' before the period at the end of the paragraph.
0
12. Section 145.43 is amended as follows:
0
a. In paragraph (b)(2)(iii), in the first sentence, by removing the
words ``either no poultry or'', and by removing the word ``were'' and
adding the word ``was'' in its place.
0
b. By removing and reserving paragraphs (d)(2) and (d)(3).
0
c. In paragraph (f)(5), by redesignating footnote 6 as footnote 5.
0
d. In paragraph (g) introductory text, by removing the words ``H5 and
H7'' and adding the word ``H5/H7'' in their place each time they
appear; and by removing the word ``serological''.
0
e. By revising paragraph (g)(1) introductory text and paragraph (g)(2)
introductory text to read as set forth below.
0
f. In paragraphs (g)(1)(i) and (g)(2)(i), by removing the words
``Provided, that primary spent fowl be tested within 30 days prior to
movement to disposal;''.
0
g. By redesignating paragraph (g)(3) as paragraph (g)(4).
0
h. By adding a new paragraph (g)(3) to read as set forth below.
Sec. 145.43 Terminology and classification; flocks and products.
* * * * *
(g) * * *
(1) It is a primary breeding flock in which a minimum of 30 birds
have been tested negative to the H5/H7 subtypes of avian influenza as
provided in Sec. 145.14(d) when more than 4 months of age and prior to
the onset of egg production. To retain this classification:
* * * * *
(2) It is a multiplier breeding flock in which a minimum of 30
birds have been tested negative to the H5/H7 subtypes of avian
influenza as provided in Sec. 145.14(d) when more than 4 months of age
and prior to the onset of egg production. To retain this
classification:
* * * * *
(3) During each 90-day period, all spent fowl, up to a maximum of
30, must be tested and found negative within 21 days prior to movement
to slaughter.
* * * * *
Sec. 145.44 [Amended]
0
13. In Sec. 145.44, paragraph (a)(1)(i) is amended by removing the
word ``and''; and by adding the words ``, Sec. 145.73(b)(2)(i), Sec.
145.83(b)(2)(i), and Sec. 145.93(b)(3)(i) through (vii)'' before the
period at the end of the paragraph.
Subpart E--Special Provisions for Hobbyist and Exhibition
Waterfowl, Exhibition Poultry, and Game Bird Breeding Flocks and
Products
0
14. The heading for subpart E is revised to read as set forth above.
0
15. In Sec. 145.52, the introductory text is revised to read as
follows:
Sec. 145.52 Participation.
Participating flocks of hobbyist and exhibition waterfowl,
exhibition poultry, and game birds, and the eggs
[[Page 15794]]
and baby poultry produced from them shall comply with the applicable
general provisions of subpart A of this part and the special provisions
of this subpart E. The special provisions that apply to meat-type
waterfowl flocks are found in subpart I of this part.
0
16. Section 145.53 is amended as follows:
0
a. In paragraph (b)(2)(iii), in the first sentence, by removing the
words ``either no poultry or'', and by removing the word ``were'' and
adding the word ``was'' in its place.
0
b. In paragraph (b)(5), by adding the words ``hobbyist or exhibition''
before the word ``waterfowl''.
0
c. In paragraph (e) in the introductory text, second sentence, by
adding the words ``hobbyist or exhibition'' before the word
``waterfowl''; and by removing the word ``serological''.
0
d. In the introductory text of paragraph (e)(1), by removing the words
``for antibodies''; and by removing the words ``by the agar gel
immunodiffusion test specified in Sec. 147.9 of this chapter'' and
adding the words ``as provided in Sec. 145.14(d)'' in their place.
0
e. In the introductory text of paragraph (e)(2), by removing the words
``for antibodies''; and by removing the words ``by the agar gel
immunodiffusion test specified in Sec. 147.9 of this chapter'' and
adding the words ``as provided in Sec. 145.14(d)'' in their place.
0
f. By adding a new paragraph (e)(3) to read as set forth below.
Sec. 145.53 Terminology and classification; flocks and products.
* * * * *
(e) * * *
(3) During each 90-day period, all spent fowl, up to a maximum of
30, must be tested and found negative within 21 days prior to movement
to slaughter.
* * * * *
Sec. 145.54 [Amended]
0
17. In Sec. 145.54, paragraph (a)(1)(i) is amended by removing the
word ``and''; and by adding the words ``, Sec. 145.73(b)(2)(i), Sec.
145.83(b)(2)(i), and Sec. 145.93(b)(3)(i) through (vii)'' before the
period at the end of the paragraph.
0
18. Section 145.73 is amended as follows:
0
a. In the introductory text of paragraph (f), second sentence, by
removing the word ``serological.''
0
b. By revising paragraph (f)(1) and adding a new paragraph (f)(2) to
read as set forth below.
Sec. 145.73 Terminology and classification; flocks and products.
* * * * *
(f) * * *
(1) It is a primary breeding flock in which a minimum of 30 birds
have been tested negative for antibodies to avian influenza when more
than 4 months of age. To retain this classification:
(i) A sample of at least 30 birds must be tested negative at
intervals of 90 days; or
(ii) A sample of fewer than 30 birds may be tested, and found to be
negative, at any one time if all pens are equally represented and a
total of 30 birds is tested within each 90-day period; or
(iii) The flock is tested as provided in Sec. 145.14(d) at
intervals of 30 days or less and found to be negative, and a total of
30 samples are collected and tested within each 90-day period; and
(2) During each 90-day period, all primary spent fowl, up to a
maximum of 30, must be tested serologically and found negative within
21 days prior to movement to slaughter.
0
19. Section 145.83 is amended as follows:
0
a. In paragraph (f)(1)(vi), by removing the semicolon at the end of the
paragraph and adding a period in its place; and by adding a new
sentence at the end of the paragraph to read as set forth below.
0
b. In paragraph (f)(1)(vii), by adding the words ``to allow for the
serological testing required under paragraph (f)(1)(vi) of this
section'' after the word ``age''.
0
c. By adding a new paragraph (f)(1)(viii) to read as set forth below.
0
d. In paragraph (f)(3), by removing the words ``this classification''
and adding the words ``paragraphs (f)(1)(i) through (f)(1)(vii) of this
section'' in their place.
0
e. In the introductory text of paragraph (g), second sentence, by
removing the word ``serological.''
0
f. By revising paragraph (g)(1) and adding a new paragraph (g)(2) to
read as set forth below.
Sec. 145.83 Terminology and classification; flocks and products.
* * * * *
(f) * * *
(1) * * *
(vi) * * * All Salmonella isolates from a flock shall be
serogrouped and shall be reported to the Official State Agency on a
monthly basis;
* * * * *
(viii) Any flock entering the production period that is in
compliance with all the requirements of Sec. 145.83(f) with no history
of Salmonella isolations shall be considered ``Salmonella negative''
and may retain this definition as long as no environmental or bird
Salmonella isolations are identified and confirmed from the flock or
flock environment by sampling on 4 separate collection dates over a
minimum of a 2-week period. Sampling and testing must be performed as
described in paragraph (f)(1)(vi) of this section. An unconfirmed
environmental Salmonella isolation shall not change this Salmonella
negative status.
* * * * *
(g) * * *
(1) It is a primary breeding flock in which a minimum of 30 birds
have been tested negative for antibodies to avian influenza when more
than 4 months of age. To retain this classification:
(i) A sample of at least 30 birds must be tested negative at
intervals of 90 days; or
(ii) A sample of fewer than 30 birds may be tested, and found to be
negative, at any one time if all pens are equally represented and a
total of 30 birds is tested within each 90-day period; or
(iii) The flock is tested as provided in Sec. 145.14(d) at
intervals of 30 days or less and found to be negative, and a total of
30 samples are collected and tested within each 90-day period; and
(2) During each 90-day period, all primary spent fowl, up to a
maximum of 30, must be tested serologically and found negative within
21 days prior to movement to slaughter.
0
20. A new subpart I, consisting of Sec. Sec. 145.91 through 145.94, is
added to read as follows:
Subpart I--Special Provisions for Meat-Type Waterfowl Breeding Flocks
and Products
Sec.
145.91 Definitions.
145.92 Participation.
145.93 Terminology and classification; flocks and products.
145.94 Terminology and classification; States.
Subpart I--Special Provisions for Meat-Type Waterfowl Breeding
Flocks and Products
Sec. 145.91 Definitions.
Except where the context otherwise requires, for the purposes of
this subpart the following term shall be construed to mean:
Meat-type waterfowl breeding flocks. Flocks of domesticated duck or
goose that are composed of stock that has been developed and is
maintained for the primary purpose of producing baby poultry that will
be raised under confinement for the primary purpose of producing meat
for human consumption.
Sec. 145.92 Participation.
Participating flocks of meat-type waterfowl and the eggs and baby
poultry
[[Page 15795]]
produced from them shall comply with the applicable general provisions
of subpart A of this part and the special provisions of this subpart I.
(a) Started poultry shall lose their identity under Plan
terminology when not maintained by Plan participants under the
conditions prescribed in Sec. 145.5(a).
(b) Hatching eggs produced by primary breeding flocks shall be
fumigated (see Sec. 147.25 of this chapter) or otherwise sanitized.
(c) Any nutritive material provided to baby poultry must be free of
the avian pathogens that are officially represented in the Plan disease
classifications listed in Sec. 145.10.
Sec. 145.93 Terminology and classification; flocks and products.
Participating flocks, and the eggs and baby poultry produced from
them, that have met the respective requirements specified in this
section may be designated by the following terms and the corresponding
designs illustrated in Sec. 145.10.
(a) [Reserved]
(b) U.S. Pullorum-Typhoid Clean. A flock in which freedom from
pullorum and typhoid has been demonstrated to the Official State Agency
under the criteria in one of the following paragraphs (b)(1) through
(b)(5) of this section (See Sec. 145.14 relating to the official blood
test where applicable.):
(1) It has been officially blood tested within the past 12 months
with no reactors.
(2) It is a multiplier breeding flock, or a breeding flock composed
of progeny of a primary breeding flock which is intended solely for the
production of multiplier breeding flocks, and meets the following
specifications as determined by the Official State Agency and the
Service:
(i) The flock is located in a State where all persons performing
poultry disease diagnostic services within the State are required to
report to the Official State Agency within 48 hours the source of all
poultry specimens from which S. pullorum or S. gallinarum is isolated;
(ii) The flock is composed entirely of birds that originated from
U.S. Pullorum-Typhoid Clean breeding flocks or from flocks that met
equivalent requirements under official supervision; and
(iii) The flock is located on a premises where a flock not
classified as U.S. Pullorum-Typhoid Clean was located the previous
year; Provided, that an Authorized Testing Agent must blood test up to
300 birds per flock, as described in Sec. 145.14, if the Official
State Agency determines that the flock has been exposed to pullorum-
typhoid. In making determinations of exposure and setting the number of
birds to be blood tested, the Official State Agency shall evaluate the
results of any blood tests, described in Sec. 145.14(a)(1), that were
performed on an unclassified flock located on the premises during the
previous year; the origins of the unclassified flock; and the
probability of contacts between the flock for which qualification is
being sought and infected wild birds, contaminated feed or waste, or
birds, equipment, supplies, or personnel from flocks infected with
pullorum-typhoid.
(3) It is a multiplier breeding flock that originated from U.S.
Pullorum-Typhoid Clean breeding flocks or from flocks that met
equivalent requirements under official supervision, and is located in a
State in which it has been determined by the Service that:
(i) All hatcheries within the State are qualified as ``National
Plan Hatcheries'' or have met equivalent requirements for pullorum-
typhoid control under official supervision;
(ii) All hatchery supply flocks within the State are qualified as
U.S. Pullorum-Typhoid Clean or have met equivalent requirements for
pullorum-typhoid control under official supervision: Provided, That if
other domesticated fowl are maintained on the same premises as the
participating flock, freedom from pullorum-typhoid infection shall be
demonstrated by an official blood test of each of these fowl;
(iii) All shipments of products other than U.S. Pullorum-Typhoid
Clean, or equivalent, into the State are prohibited;
(iv) All persons performing poultry disease diagnostic services
within the State are required to report to the Official State Agency
within 48 hours the source of all poultry specimens from which S.
pullorum or S. gallinarum is isolated;
(v) All reports of any disease outbreak involving a disease covered
under the Plan are promptly followed by an investigation by the
Official State Agency to determine the origin of the infection;
Provided, That if the origin of the infection involves another State,
or if there is exposure to poultry in another State from the infected
flock, then the National Poultry Improvement Plan will conduct an
investigation;
(vi) All flocks found to be infected with pullorum or typhoid are
quarantined until marketed or destroyed under the supervision of the
Official State Agency, or until subsequently blood tested, following
the procedure for reacting flocks as contained in Sec. 145.14(a)(5),
and all birds fail to demonstrate pullorum or typhoid infection;
(vii) All poultry, including exhibition, exotic, and game birds,
but excluding waterfowl, going to public exhibition shall come from
U.S. Pullorum-Typhoid Clean or equivalent flocks, or have had a
negative pullorum-typhoid test within 90 days of going to public
exhibition;
(viii) Discontinuation of any of the conditions or procedures
described in paragraphs (a)(3)(i), (ii), (iii), (iv), (v), (vi), and
(vii) of this section, or the occurrence of repeated outbreaks of
pullorum or typhoid in poultry breeding flocks within or originating
within the State shall be grounds for the Service to revoke its
determination that such conditions and procedures have been met or
complied with. Such action shall not be taken until a thorough
investigation has been made by the Service and the Official State
Agency has been given an opportunity to present its views.
(4) It is a multiplier breeding flock located in a State which has
been determined by the Service to be in compliance with the provisions
of paragraph (a)(3) of this section, and in which pullorum disease or
fowl typhoid is not known to exist nor to have existed in hatchery
supply flocks within the State during the preceding 24 months.
(5) It is a primary breeding flock located in a State determined to
be in compliance with the provisions of paragraph (a)(4) of this
section, and in which a sample of 300 birds from flocks of more than
300, and each bird in flocks of 300 or less, has been officially tested
for pullorum-typhoid within the past 12 months with no reactors:
Provided, That when a flock is a primary breeding flock located in a
State which has been deemed to be a U.S. Pullorum-Typhoid Clean State
for the past 3 years, and during which time no isolation of pullorum or
typhoid has been made that can be traced to a source in that State, a
bacteriological examination monitoring program or a serological
examination monitoring program acceptable to the Official State Agency
and approved by the Service may be used in lieu of annual blood
testing.
(c) U.S. H5/H7 Avian Influenza Clean. This program is intended to
be the basis from which the breeding-hatchery industry may conduct a
program for the prevention and control of the H5/H7 subtypes of avian
influenza. It is intended to determine the presence of the H5/H7
subtypes of avian influenza in meat-type waterfowl breeding flocks
through routine surveillance of each participating breeding flock. A
flock, and the hatching eggs and baby poultry
[[Page 15796]]
produced from it, will qualify for this classification when the
Official State Agency determines that it has met one of the following
requirements:
(1) It is a primary breeding flock in which a minimum of 30 birds
have been tested negative to the H5/H7 subtypes of avian influenza as
provided in Sec. 145.14(d) when more than 4 months of age. To retain
this classification:
(i) A sample of at least 30 birds must be tested and found to be
negative at intervals of 90 days; or
(ii) A sample of fewer than 30 birds may be tested, and found to be
negative, at any one time if all pens are equally represented and a
total of 30 birds are tested within each 90-day period.
(2) It is a multiplier breeding flock in which a minimum of 30
birds have been tested negative to the H5/H7 subtypes of avian
influenza as provided in Sec. 145.14(d) when more than 4 months of
age. To retain this classification:
(i) A sample of at least 30 birds must be tested negative at
intervals of 180 days; or
(ii) A sample of fewer than 30 birds may be tested, and found to be
negative, at any one time if all pens are equally represented and a
total of 30 birds are tested within each 180-day period.
(3) During each 90-day period, all spent fowl, up to a maximum of
30, must be tested serologically and found negative within 21 days
prior to movement to slaughter.
Sec. 145.94 Terminology and classification; States.
(a) U.S. Pullorum-Typhoid Clean State. (1) A State will be declared
a U.S. Pullorum-Typhoid Clean State when it has been determined by the
Service that:
(i) The State is in compliance with the provisions contained in
Sec. Sec. 145.23(b)(3)(i) through (vii), 145.33(b)(3)(i) through
(vii), 145.43(b)(3)(i) through (vi), 145.53(b)(3)(i) through (vii),
145.73(b)(2)(i), 145.83(b)(2)(i), and 145.93(b)(3)(i) through (vii).
(ii) No pullorum disease or fowl typhoid is known to exist nor to
have existed in hatchery supply flocks within the State during the
preceding 12 months: Provided, That pullorum disease or fowl typhoid
found within the preceding 24 months in waterfowl, exhibition poultry,
and game bird breeding flocks will not prevent a State that is
otherwise eligible from qualifying.
(2) Discontinuation of any of the conditions described in paragraph
(a)(1)(i) of this section, or repeated outbreaks of pullorum or typhoid
occur in hatchery supply flocks described in paragraph (a)(1)(ii) of
this section, or if an infection spreads from the originating premises,
the Service shall have grounds to revoke its determination that the
State is entitled to this classification. Such action shall not be
taken until a thorough investigation has been made by the Service and
the Official State Agency has been given an opportunity for a hearing
in accordance with rules of practice adopted by the Administrator.
(b) [Reserved]
PART 146--NATIONAL POULTRY IMPROVEMENT PLAN FOR COMMERCIAL POULTRY
0
21. The authority citation for part 146 continues to read as follows:
Authority: 7 U.S.C. 8301-8317; 7 CFR 2.22, 2.80, and 371.4.
0
22. Section 146.1 is amended as follows:
0
a. By revising the definitions of commercial table-egg layer flock and
H5/H7 low pathogenic avian influenza (LPAI) to read as set forth below.
0
b. By adding, in alphabetical order, a new definition of commercial
table-egg layer pullet flock to read as set forth below.
Sec. 146.1 Definitions.
* * * * *
Commercial table-egg layer flock. All table-egg layers of common
age or pullet source on one premises.
* * * * *
Commercial table-egg layer pullet flock. A table-egg layer flock
prior to the onset of egg production.
* * * * *
H5/H7 low pathogenic avian influenza (LPAI). An infection of
poultry caused by an influenza A virus of H5 or H7 subtype that has an
intravenous pathogenicity index in 6-week-old chickens less than 1.2 or
less than 75 percent mortality in 4- to 8-week-old chickens infected
intravenously, or an infection with influenza A viruses of H5 or H7
subtype with a cleavage site that is not consistent with a previously
identified highly pathogenic avian influenza virus.
* * * * *
0
23. Section 146.9 is amended by revising the introductory text to read
as follows:
Sec. 146.9 Terminology and classification; flocks, products, and
States.
Participating flocks, products produced from them, and States that
have met the requirements of a classification in this part may be
designated by the corresponding illustrative design in this section.
* * * * *
0
24. Section 146.21 is amended by adding a new definition of table-egg
layer pullet in alphabetical order to read as follows:
Sec. 146.21 Definitions.
* * * * *
Table-egg layer pullet. A sexually immature domesticated chicken
grown for the primary purpose of producing eggs for human consumption.
0
25. In Sec. 146.23, paragraph (a) is revised to read as follows:
Sec. 146.23 Terminology and classification; flocks and products.
* * * * *
(a) U.S. H5/H7 Avian Influenza Monitored. This program is intended
to be the basis from which the table-egg layer industry may conduct a
program to monitor for the H5/H7 subtypes of avian influenza. It is
intended to determine the presence of the H5/H7 subtypes of avian
influenza in table-egg layers and table-egg layer pullets through
routine surveillance of each participating commercial table-egg layer
and table-egg layer pullet flock. A flock will qualify for this
classification when the Official State Agency determines that it has
met one of the following requirements:
(1) Table-egg layer pullet flocks. (i) It is a commercial table-egg
layer pullet flock in which a minimum of 11 birds have been tested
negative to the H5/H7 subtypes of avian influenza as provided in Sec.
146.13(b) within 30 days prior to movement; or
(ii) It is a commercial table-egg layer pullet flock that has an
ongoing active and diagnostic surveillance program for the H5/H7
subtypes of avian influenza in which the number of birds tested is
equivalent to the number required in paragraph (a)(1)(i) of this
section and that is approved by the Official State Agency and the
Service.
(2) Table-egg layer flocks. (i) It is a commercial table-egg layer
flock in which a minimum of 11 birds have been tested negative to the
H5/H7 subtypes of avian influenza as provided in Sec. 146.13(b) within
30 days prior to disposal;
(ii) It is a commercial table-egg layer flock in which a minimum of
11 birds have been tested negative for the H5/H7 subtypes of avian
influenza as provided in Sec. 146.13(b) within a 12-month period; or
(iii) It is a commercial table-egg layer flock that has an ongoing
active and diagnostic surveillance program for the H5/H7 subtypes of
avian influenza in
[[Page 15797]]
which the number of birds tested is equivalent to the number required
in paragraph (a)(2)(i) or paragraph (a)(2)(ii) of this section and that
is approved by the Official State Agency and the Service.
* * * * *
Sec. 146.24 [Amended]
0
26. Section 146.24 is amended as follows:
0
a. In paragraph (a)(1)(i), by adding the words ``and all commercial
table-egg layer pullet flocks that supply those flocks'' after the word
``flocks''.
0
b. In paragraphs (a)(1)(iii) through (a)(1)(v), by adding the words
``and table-egg layer pullet'' after the word ``layer'' each time it
occurs.
Sec. 146.33 [Amended]
0
27. In Sec. 146.33, paragraphs (a)(1) and (a)(2) are amended by adding
the words ``, as provided in Sec. 146.13(b),'' after the word
``influenza,'' each time it occurs.
Sec. 146.43 [Amended]
0
28. In Sec. 146.43, paragraph (a)(1) is amended by adding the words
``, as provided in Sec. 146.13(b),'' after the word ``influenza'' and
by removing the word ``virus''.
Sec. 146.53 [Amended]
0
29. Section 146.53 is amended as follows:
0
a. In paragraph (a)(1), by adding the words ``, as provided in Sec.
146.13(b),'' after the word ``influenza.''
0
b. In paragraph (a)(2), by removing the words ``antibodies to'' and by
adding the words ``, as provided in Sec. 146.13(b),'' after the word
``influenza.''
0
c. In paragraph (b), in the last sentence, by adding the words ``, as
provided in Sec. 146.13(b),'' after the word ``influenza.''
PART 147--AUXILIARY PROVISIONS ON NATIONAL POULTRY IMPROVEMENT PLAN
0
30. The authority citation for part 147 continues to read as follows:
Authority: 7 U.S.C. 8301-8317; 7 CFR 2.22, 2.80, and 371.4.
Sec. 147.5 [Amended]
0
31. In Sec. 147.5, footnote 4 to paragraph (b) is amended by removing
the words ``1498 Klondike Road, Suite 200'' and adding the words ``1506
Klondike Road, Suite 300'' in their place.
0
32. Section 147.6 is amended as follows:
0
a. By revising the introductory text and paragraphs (a)(1) through
(a)(4) to read as set forth below.
0
b. By removing paragraphs (a)(5) through (a)(15).
Sec. 147.6 Procedures for determining the status of flocks reacting
to test for Mycoplasma gallisepticum, Mycoplasma synoviae, and
Mycoplasma melagridis.
Procedures for isolation and identification of Mycoplasma may be
found in Isolation and Identification of Avian Pathogens, published by
the American Association of Avian Pathologists; Kleven, S.H., F.T.W.
Jordan, and J.M. Bradbury, Avian Mycoplasmosis (Mycoplasma
gallisepticum), Manual of Diagnostic Tests and Vaccines for Terrestrial
Animals, Fifth Ed., Office International des Epizooties, pp 842-855,
2004; and Sec. Sec. 147.15 and 147.16.
(a) * * *
(1) If the tube agglutination test, enzyme-labeled immunosorbent
assay (ELISA), official molecular examination procedure, or serum plate
test is negative, the flock qualifies for the classification for which
it was tested.
(2) If the tube agglutination, ELISA, or serum plate test is
positive, the hemaglutination inhibition (HI) test or a molecular
examination procedure shall be conducted: Provided, for the HI test,
that if more than 50 percent of the samples are positive for M.
gallisepticum, M. meleagridis, or M. synoviae, the HI test shall be
conducted on 10 percent of the positive samples or 25 positive samples,
whichever is greater. HI titers of 1:40 or more may be interpreted as
suspicious and appropriate antigen detection samples should be taken
promptly (within 7 days of the original sampling) from 30 clinically
affected birds and examined by an approved cultural technique
individually, or pooled (up to 5 swabs per test) and used in a
molecular examination procedure or in vivo bioassay.
(3) If the in vivo bioassay, molecular examination procedure, or
culture procedure is negative, the Official State Agency may qualify
the flock for the classification for which it was tested. In the event
of contaminated cultures, the molecular examination technique must be
used to make a final determination.
(4) If the in vivo bioassay, molecular examination procedure, or
culture procedure is positive, the flock will be considered infected.
* * * * *
Sec. Sec. 147.12, 147.14, 147.15, 147.16, 147.30, and
147.31 [Amended]
0
33. In Sec. Sec. 147.12, 147.14, 147.15, 147.16, 147.30, and 147.31,
footnotes 9 through 21 are redesignated as footnotes 10 through 22,
respectively.
0
34. Section 147.12 is amended as follows:
0
a. In footnote 8 to paragraph (a)(3), by removing the words ``1498
Klondike Road, Suite 200'' and adding the words ``1506 Klondike Road,
Suite 300'' in their place.
0
b. By adding a new paragraph (a)(6) and a new footnote 9 to read as set
forth below.
0
c. In newly redesignated footnote 10 to paragraph (c)(3)(ii)(A), by
removing the words ``1498 Klondike Road, Suite 200'' and adding the
words ``1506 Klondike Road, Suite 300'' in their place.
Sec. 147.12 Procedures for collection, isolation, and identification
of Salmonella from environmental samples, cloacal swabs, chick box
papers, and meconium samples.
* * * * *
(a) * * *
(6) Shoe cover sampling technique. Absorbable fabric shoe covers
involve the exposure of the bottom surface of shoe covers to the
surface of floor litter and slat areas. Wearing clean latex gloves,
place the shoe covers over footwear that is only worn inside the
poultry house. This can be footwear dedicated to the facility or
disposable overshoes. Each pair of shoe covers should be worn while
walking at a normal pace over a distance of 305 meters (1,000 feet).
For flocks with fewer than 500 breeders, at least 1 pair of shoe covers
should be worn to sample the floor of the bird area. For flocks with
500 or more breeders, at least 2 pairs of shoe covers should be worn to
sample the floor of the bird area. After sampling, place each shoe
cover in a sterile container with 30 ml of double strength skim
milk.\9\ Seal the sterile containers and promptly refrigerate them at 2
to 4 [deg]C or place in a cooler with ice or ice packs. Do not freeze.
Samples should be stored at refrigerator temperatures of 2 to 4 [deg]C
no more than 5 days prior to culturing.
---------------------------------------------------------------------------
\9\ Obtain procedure for preparing double strength skim milk
from USDA-APHIS ``Recommended Sample Collection Methods for
Environmental Samples,'' available from the National Poultry
Improvement Plan, Veterinary Services, APHIS, USDA, 1506 Klondike
Road, Suite 300, Conyers, GA 30094.
---------------------------------------------------------------------------
* * * * *
0
35. In Sec. 147.45, the first sentence is revised to read as follows:
Sec. 147.45 Official delegates.
Each cooperating State shall be entitled to one official delegate
for each of the programs prescribed in parts 145 and 146 of this
chapter in which it has one or more participants at the time of the
Conference. * * *
[[Page 15798]]
0
36. In Sec. 147.52, a new paragraph (c) is added to read as follows:
Sec. 147.52 Approved tests.
* * * * *
(c) The following diagnostic test kits that are not licensed by the
Service (e.g., bacteriological culturing kits) are approved for use in
the NPIP:
(1) Rapid Chek(copyright)Select TMSalmonella Test Kit, Strategic
Diagnostics, Inc., Newark, DE 19713.
(2) ADIAFOOD Rapid Pathogen Detection System for Salmonella spp.,
AES Chemunex Canada. Laval, QC (Canada) H7L4S3.
(3) DuPont Qualicon BAX Polymerase Chain Reaction (PCR)-based assay
for Salmonella, DuPont Qualicon, Wilmington, DE 19810.
Done in Washington, DC, this 16th day of March 2011.
Kevin Shea,
Acting Administrator, Animal and Plant Health Inspection Service.
[FR Doc. 2011-6539 Filed 3-21-11; 8:45 am]
BILLING CODE 3410-34-P