[Federal Register Volume 78, Number 108 (Wednesday, June 5, 2013)]
[Rules and Regulations]
[Pages 33692-33698]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2013-13270]
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DEPARTMENT OF COMMERCE
Bureau of Industry and Security
15 CFR Parts 740, 742, and 774
[Docket No. 120806310-2310-01]
RIN 0694-AF76
Implementation of the Understandings Reached at the 2012
Australia Group (AG) Plenary Meeting and the 2012 AG Intersessional
Decisions; Changes to Select Agent Controls
AGENCY: Bureau of Industry and Security, Commerce.
ACTION: Final rule.
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SUMMARY: The Bureau of Industry and Security (BIS) publishes this final
rule to amend the Export Administration Regulations (EAR) to implement
the understandings reached at the June 2012 plenary meeting of the
Australia Group (AG) and the 2012 AG intersessional decisions.
Specifically, this rule amends the Commerce Control List (CCL) entry in
the EAR that controls human and zoonotic pathogens and ``toxins'' to
reflect changes to the AG ``List of Biological Agents for Export
Control'' that were made based on the understandings adopted at the
June 2012 AG plenary meeting. These changes included the addition of
three pathogens and clarifications to two other items. This rule also
amends the CCL entry in the EAR that controls plant pathogens to
reflect: The 2012 AG Plenary agreement to add five pathogens to the AG
``List of Plant Pathogens for Export Control;'' and the AG
intersessional clarifications to six pathogens identified on this AG
list. In addition, the CCL entry in the EAR that controls equipment
capable of handling biological materials is amended to reflect the 2012
AG intersessional decision to add certain spray-drying equipment to the
AG ``Control List of Dual-Use Biological Equipment and Related
Technology and Software.'' This rule also removes the CCL entry that
controls select agents not identified on any of the AG common controls
lists, but identified on the CCL because they are (or were, until
recently) subject to controls maintained by the Centers for Disease
Control and Prevention (CDC), U.S. Department of Health and Human
Services, and the Animal and Plant Health Inspection Service (APHIS),
U.S. Department of Agriculture, on their possession, use, and transfer
within the United States. Rather than continuing to control these
select agents in a separate CCL entry, this rule adds those select
agents that remain subject to the CDC/APHIS controls (as well as a
recent addition to the list of select agents) to the AG-related CCL
entries that control human and zoonotic pathogens and ``toxins'' and
plant pathogens, respectively.
DATES: This rule is effective June 5, 2013.
ADDRESSES: Send comments regarding this collection of information,
including suggestions for reducing the burden, to Jasmeet Seehra,
Office of Management and Budget (OMB), by email to Jasmeet_K._Seehra@omb.eop.gov, or by fax to (202) 395-7285; and to the Regulatory
Policy Division, Bureau of Industry and Security, Department of
Commerce, 14th Street & Pennsylvania Avenue NW., Room 2705, Washington,
DC 20230.
FOR FURTHER INFORMATION CONTACT: Elizabeth Sangine, Director, Chemical
and Biological Controls Division, Office of Nonproliferation and Treaty
Compliance, Bureau of Industry and Security, Telephone: (202) 482-3343.
SUPPLEMENTARY INFORMATION:
Background
The Bureau of Industry and Security (BIS) is amending the Export
Administration Regulations (EAR) to implement the understandings
reached at the Australia Group (AG) plenary meeting held in Paris,
France, on June 12-15, 2012. This rule also implements the
recommendations presented at the AG intersessional implementation
meeting held in Ottawa, Canada, on February 14-16, 2012, and adopted
pursuant to the AG silent approval procedure, which closed on March 23,
2012. The AG is a multilateral forum consisting of 40 participating
countries that maintain export controls on a list of chemicals,
biological agents, and related equipment and technology that could be
used in a chemical or biological weapons program. The AG periodically
reviews items on its control list to enhance the effectiveness of
participating governments' national controls and to achieve greater
harmonization among these controls.
June 2012 AG Plenary Changes
The June 2012 AG plenary meeting adopted understandings that
affected the AG ``List of Biological Agents for Export Control'' and
the AG ``List of Plant Pathogens for Export Control.''
This rule amends Export Control Classification Number (ECCN) 1C351
to reflect the AG plenary changes to the ``List of Biological Agents
for Export Control.'' Specifically, ECCN 1C351 (Human and zoonotic
pathogens and ``toxins'') is amended by adding botulinum neurotoxin
producing strains of the following bacteria to 1C351.c: Clostridium
argentinense (formerly known as Clostridium botulinum Type G);
Clostridium baratii; and Clostridium butyricum. ECCN 1C351.c is
partially renumbered to control these bacteria under 1C351.c.8., .c.9,
and .c.11, respectively, while the bacteria previously controlled under
these subparagraphs (Clostridium botulinum; Clostridium perfringens,
epsilon toxin producing types; and Coxiella burnetii) are now
controlled under 1C351.c.10, .c.12. and .c.13, respectively. In
addition, bacteria previously controlled under 1C351.c.12 through .c.17
are now controlled under 1C351.c.14 through
[[Page 33693]]
.c.16 (Francisella tularensis; Rickettsia prowazekii; and Salmonella
typhi) and 1C351.c.18 through .c 20 (Shigella dysenteriae; Vibrio
cholerae; and Yersinia pestis). Also note, with respect to ECCN
1C351.c.15 as amended by this rule, that the listing for the bacterium
``Rickettsia prowasecki (a.k.a. Rickettsia prowazekii)'' is amended to
read ``Rickettsia prowazekii,'' consistent with the listing of this
bacterium in the AG ``List of Biological Agents for Export Control''
and the commonly accepted spelling of this bacterium within the
scientific community.
This rule also amends ECCN 1C351.c to clarify that the controls on
``Escherichia coli and other verotoxin producing serotypes'' apply to
``Shiga toxin producing Escherichia coli (STEC) of serogroups O26, O45,
O103, O104, O111, O121, O145, O157, and other shiga toxin producing
serogroups.'' These bacteria are now controlled under 1C351.c.17. Prior
to the publication of this rule and the partial renumbering of 1C351.c,
these bacteria were controlled under 1C351.c.11. In addition, this rule
amends 1C351.d.14 to clarify that the controls on ``Staphylococcus
aureus toxins'' apply to ``Staphylococcus aureus enterotoxins,
hemolysin alpha toxin, and toxic shock syndrome toxin (formerly known
as Staphylococcus enterotoxin F).''
This rule amends ECCN 1C354 (Plant pathogens) to reflect the AG
plenary changes to the ``List of Plant Pathogens for Export Control.''
Specifically, ECCN 1C354 is amended by adding the following five fungi
to 1C354.b: Peronosclerospora philippinensis (Peronosclerospora
sacchari); Sclerophthora rayssiae var. zeae; Synchytrium endobioticum;
Tilletia indica; and Thecaphora solani. These fungi are controlled
under 1C354.b.7 through .b.11, respectively.
2012 AG Intersessional Changes
This rule also implements the recommendations presented at the AG
intersessional implementation meeting held in February 2012 and adopted
pursuant to the AG silent approval procedure. These recommendations
included changes to the AG ``List of Plant Pathogens for Export
Control'' and the AG ``Control List of Dual-Use Biological Equipment
and Related Technology and Software.'' This rule amends ECCN 1C354
(Plant pathogens) to reflect the AG intersessional changes to the
``List of Plant Pathogens for Export Control.'' Specifically, ECCN
1C354.a (Bacteria) is amended to clarify that the controls for
``Xanthomonas campestris pv. citri'' in 1C354.a.2 apply to
``Xanthomonas axonopodis pv. citri (Xanthomonas campestris pv. citri A)
(Xanthomonas campestris pv. citri)'' and that the controls for
``Ralstonia solanacearum'' in 1C354.a.5 apply to ``Ralstonia
solanacearum, race 3, biovar 2.'' This rule also amends ECCN 1C354.b
(Fungi) to reorder the wording of the controls for ``Colletotrichum
coffeanum var. virulans (Colletotrichum kahawae)'' in 1C354.b.1 to read
``Colletotrichum kahawae (Colletotrichum coffeanum var. virulans).'' In
addition, this rule amends the controls for ``Puccinia graminis'' in
1C354.b.4 to clarify that they apply to ``Puccinnia graminis ssp.
graminis var. graminis/Puccinia graminis ssp. graminis var. stakmanii
(Puccinia graminis [syn. Puccinia graminis f. sp. tritici])'' and the
controls for ``Magnaporthe grisea'' in 1C354.b.6 to clarify that they
apply to ``Magnaporthe oryzae (Pyricularia oryzae).'' Furthermore, this
rule amends 1C354.c to clarify the controls for ``Potato Andean latent
tymovirus'' in 1C354.c.1 to read ``Andean potato latent virus (Potato
Andean latent tymovirus).''
In addition, this rule amends ECCN 2B352 (Equipment capable of use
in handling biological materials) to reflect the AG intersessional
changes to the ``Control List of Dual-Use Biological Equipment and
Related Technology and Software.'' Specifically, this rule adds
controls for certain spray-drying equipment under 2B352.f. Those items
that were controlled under 2B352.f through .h, prior to the publication
of this rule, are now controlled under 2B352.g through .i,
respectively. ECCN 2B352.f, as revised by this rule, now controls
spray-drying equipment capable of drying toxins or pathogenic
microorganisms and having all of the following characteristics: (1) A
water evaporation capacity of >= 0.4 kg/h and <= 400 kg/h; (2) the
ability to generate a typical mean product particles size of <= 10
micrometers with existing fittings or by minimal modification of the
spray-dryer with atomization nozzles enabling generation of the
required particle size; and (3) capable of being sterilized or
disinfected in situ.
Select Agent Changes to the CCL
This rule removes ECCN 1C360 (Select agents). This ECCN controlled
select agents not included on any of the AG common controls lists that
were identified on the CCL because they are (or were, until recently)
subject to controls maintained by the Animal and Plant Health
Inspection Service (APHIS), U.S. Department of Agriculture, and the
Centers for Disease Control and Prevention (CDC), U.S. Department of
Health and Human Services, on their possession, use, and transfer
within the United States.
As a result of amendments by CDC to the list of ``HHS select
agents'' in 42 CFR 73.3 and the list of ``Overlap select agents and
toxins'' in 42 CFR 73.4 and amendments by APHIS to the list of ``Plant
Protection and Quarantine (PPQ) select agents and toxins'' in 7 CFR
331.3 and the list of ``Veterinary Services (VS) select agents and
toxins'' in 9 CFR 121.3, ten of the eighteen select agents that were
listed in ECCN 1C360 are no longer included on the CDC/APHIS select
agents lists. For this reason, as well as to assist exporters to more
easily identify all of the select agents that are subject to the
chemical/biological (CB) controls described in Section 742.2(a)(1) of
the EAR (i.e., CB Column 1), BIS is removing ECCN 1C360 from the CCL
and adding the select agents that were controlled by ECCN 1C360, and
continue to be identified on the CDC/APHIS lists, to the appropriate
AG-related ECCNs on the CCL (i.e., ECCNs 1C351 and 1C354). Prior to the
publication of this rule, the CDC/APHIS select agents listed in these
ECCNs included only those select agents that were also identified on
one of the AG common control lists.
As a result of the changes described above, the following select
agents that were controlled by ECCN 1C360 are no longer listed on the
CCL: Central European tick-borne encephalitis viruses (i.e.,
Absettarov, Hanzalova, Hypr, and Kumlinge); Cercopithecine herpesvirus
1 (Herpes B virus); Flexal virus; Akabane virus; Bovine spongiform
encephalopathy agent; Camel pox virus; Malignant catarrhal fever virus;
Menangle virus; Erhlichia ruminantium (a.k.a. Cowdria ruminantium); and
Xylella fastidiosa pv. citrus variegated chlorosis (CVC).
Three select agents that were controlled under ECCN 1C360 and
continue to be identified on the CDC/APHIS select agents lists are now
controlled on the CCL, as follows: Reconstructed replication competent
forms of the 1918 pandemic influenza virus containing any portion of
the coding regions of all eight gene segments (now controlled under
ECCN 1C351.b.1); Rathayibacter toxicus (now controlled under ECCN
1C354.a.6); and Phoma glycinicola, formerly Pyrenochaeta glycines (now
controlled under ECCN 1C354.b.12). None of these select agents are
identified on any of the AG common control lists; however, they
continue to be subject to CB controls (for those destinations indicated
under CB Column 1 on the Commerce Country Chart in Supplement No. 1 to
part 738 of the EAR), as well as anti-terrorism
[[Page 33694]]
(AT) controls (for those destinations indicated under AT Column 1 on
the Commerce Country Chart--Country Group E:1, in Supplement No. 1 to
part 740 of the EAR, lists those countries designated as ``terrorist-
supporting countries'' for purposes of the AT controls in the EAR).
In addition, three select agents that were controlled under ECCN
1C360, and continue to be identified on the APHIS select agents lists,
have been added to the AG ``List of Plant Pathogens for Export
Control,'' in accordance with the understandings reached at the 2012 AG
Plenary (see the discussion of the 2012 AG Plenary changes, above).
These select agents are now controlled on the CCL as follows:
Peronosclerospora philippinensis (Peronosclerospora sacchari) (now
controlled under ECCN 1C354.b.7); Sclerophthora rayssiae var. zeae (now
controlled under ECCN 1C354.b.8); and Synchytrium endobioticum (now
controlled under ECCN 1C354.b.9). This rule also amends ECCN 1C354.a.3
to include the species of proteobacteria identified as Xanthomonas
oryzae, which is identified on the APHIS list of PPQ select agents and
toxins; however, only the pathovar Xanthomonas oryzae pv. oryzae (syn.
Pseudomonas campestris pv. oryzae) is identified on the AG ``List of
Plant Pathogens for Export Control.'' Like all other items controlled
under ECCN 1C354, these select agents are subject to CB Column 1
controls, as well as AT Column 1 controls.
Furthermore, this rule eliminates redundant controls on two
bacteria of the Mycoplasma mycoides cluster: Mycoplasma capricolum
subspecies capripneumoniae and Mycoplasma mycoides subspecies mycoides
small colony. These bacteria were identified under ECCN 1C360.b.2 and
ECCN 1C352.b.1, prior to the publication of this rule, but are now
controlled under ECCN 1C352.b.1, only. Both bacteria continue to be
identified on the list of ``VS Select Agents and Toxins'' maintained by
APHIS, as well as the AG ``List of Plant Pathogens for Export
Control.'' Like all other items controlled under ECCN 1C352, these
bacteria are subject to CB Column 1 controls, as well as AT Column 1
controls.
This rule also amends ECCN 1C351 by adding SARS-associated
coronavirus (SARS-CoV) under 1C351.b.2 and tick-borne encephalitis
virus (Siberian subtype) under 1C351.b.3. Both viruses were recently
included in CDC's list of ``HHS select agents and toxins,'' but are not
identified on any of the AG common control lists. However, like all
other items controlled under ECCN 1C351, these viruses are subject to
CB Column 1 controls, as well as AT Column 1 controls. Another tick-
borne encephalitis virus (Far Eastern subtype, formerly known as
Russian Spring-Summer encephalitis virus) is controlled under ECCN
1C351.a.35 and is currently included in both CDC's list of ``HHS select
agents and toxins'' and the AG ``List of Biological Agents for Export
Control.'' This rule amends ECCN 1C351.a.35 to reflect the current
nomenclature (i.e., Far Eastern subtype) used by the International
Committee on Taxonomy of Viruses.
In addition to the select agents changes described above, this rule
makes conforming changes to Sections 740.20 and 742.2 of the EAR and to
ECCNs 1C353, 1C991, 1E001 and 1E351 to reflect the removal of ECCN
1C360 from the CCL. Specifically, Section 740.20(b)(2)(v) is amended by
removing two references to ECCN 1C360 from the description of
biological items that are not eligible for License Exception Strategic
Trade Authorization (STA). The items that were controlled under ECCN
1C360 and that remain on the CCL are now controlled under ECCN 1C351.a
or .b, ECCN 1C352 or ECCN 1C354, all of which are identified in
paragraph (b)(2)(v). Section 742.2(a)(1)(i) of the EAR is amended by
removing the reference to ECCN 1C360 from the description of the
license requirements that apply to items controlled for CB reasons to
destinations indicated under CB Column 1 on the Commerce Country Chart.
ECCN 1C353 is amended by removing references to ECCN 1C360 from the
following: The Related Controls paragraph; paragraphs a.1. and b.1. in
the Items paragraph under the List of Items Controlled; and Technical
Note 3. ECCN 1C991 is amended by removing references to ECCN 1C360 from
the fourth sentence of the Related Definitions paragraph and from
paragraph a. in the Items paragraph under the List of Items Controlled.
ECCN 1E001 is amended by removing the reference to ECCN 1C360 from the
control language for ``Country Chart--CB Column 1'' in the License
Requirements section. ECCN 1E351 is amended by removing references to
ECCN 1C360 from the ECCN heading and from the controls language for
``Country Chart--CB Column 1'' in the License Requirements section.
Finally, this rule amends ECCNs 1C351, 1C352, 1C353, and 1C354 by
revising the License Requirements Note(s) in the License Requirements
section of each ECCN to add a note indicating that ECCNs 1C351, 1C352,
1C353, and 1C354 control all biological agents or ``toxins,''
regardless of quantity or attenuation, that are identified in the List
of Items Controlled for each ECCN (or, in the case of ECCN 1C353,
genetic elements or genetically modified organisms for such agents or
``toxins''), including small quantities or attenuated strains of select
biological agents or ``toxins'' that are excluded from the lists of
select biological agents or ``toxins'' by APHIS or CDC, in accordance
with the APHIS regulations in 7 CFR part 331 or 9 CFR part 121 or the
CDC regulations in 42 CFR part 73. These changes do not affect the
scope of ECCNs 1C351, 1C352, 1C353, and 1C354 and conform with the
controls described in the AG common control lists and in the AG
``Guidelines for Transfers of Sensitive Chemical or Biological Items,''
neither of which provide an exemption from control for attenuated
strains of biological agents or toxins. In conjunction with these
changes, this rule amends the Related Controls paragraph in each of
these four ECCNs to add a sentence referencing 22 CFR part 121,
Category XIV(b), for modified biological agents and biologically
derived substances that are subject to the export licensing
jurisdiction of the U.S. Department of State, Directorate of Defense
Trade Controls.
Effect of This Rule on the Scope of the CB Controls in the EAR
The changes made by this rule only marginally affect the scope of
the EAR controls on biological agents and toxins. With the removal of
ECCN 1C360 from the CCL, ten select agents that were controlled under
this ECCN prior to the publication of this rule are no longer
identified on the CCL and are classified as EAR99, instead. All of
these select agents were recently removed from the CDC/APHIS select
agents lists. In addition, six other select agents that were controlled
under ECCN 1C360 have been moved to ECCN 1C351 or ECCN 1C354 and
continue to require a license for CB reasons to destinations indicated
under CB Column 1 on the Commerce Country Chart and for AT reasons to
destinations indicated under AT Column 1--all of these select agents
continue to be identified on the CDC/APHIS select agents lists. Two
additional select agents (Mycoplasma capricolum subspecies
capripneumoniae and Mycoplasma mycoides subspecies mycoides small
colony) also were controlled under ECCN 1C360 and continue to be
identified on the CDC/APHIS select agents lists. As indicated above,
this rule did not add these select agents to ECCN 1C352 because they
were already described in ECCN 1C352.b.1 (i.e., the ECCN 1C360 controls
on these select agents duplicated the controls in ECCN
[[Page 33695]]
1C352). This rule also adds two viruses that were recently included in
CDC's list of ``HHS select agents and toxins'' (i.e., SARS-associated
coronavirus and tick-borne encephalitis virus, Siberian subtype) to
ECCN 1C351.b.
Based on the understandings reached at the June 2012 AG Plenary
meeting, this rule also adds three bacteria to ECCN 1C351 and two fungi
to ECCN 1C354, none of which were identified on the CCL prior to the
publication of this rule. The AG Plenary also added three additional
fungi to the ``List of Plant Pathogens for Export Control,'' but these
fungi were already controlled under ECCN 1C360, based on their
inclusion by APHIS on the list of PPQ select agents and toxins (7 CFR
part 331), and are now controlled under ECCN 1C354 (i.e., these fungi
are among the six select agents that have been moved by this rule from
ECCN 1C360 to ECCN 1C351 or ECCN 1C354, as indicated above).
To summarize the biological agent and toxin changes described
above, this rule removes ten CDC/APHIS select agents from the CCL,
while adding three AG-listed bacteria and two fungi, as well as two
viruses that were recently identified on CDC's list of ``HHS select
agents and toxins.'' These changes are not expected to significantly
affect the scope of the EAR controls on biological agents and toxins,
because BIS estimates that there will be no increase in the number of
license applications for these items.
Finally, this rule expands the scope of the EAR controls that apply
to dual-use equipment capable of handling biological materials by
amending ECCN 2B352 to add certain spray-drying equipment. This change
is not expected to significantly affect the scope of the EAR controls
on such equipment, because BIS anticipates only a small increase in the
number of license applications.
Although the Export Administration Act expired on August 20, 2001,
the President, through Executive Order 13222 of August 17, 2001, 3 CFR,
2001 Comp., p. 783 (2002), as amended by Executive Order 13637 of March
8, 2013, 78 FR 16129 (March 13, 2013), and as extended by the Notice of
August 15, 2012, 77 FR 49699 (August 16, 2012), has continued the EAR
in effect under the International Emergency Economic Powers Act.
Rulemaking Requirements
1. Executive Orders 13563 and 12866 direct agencies to assess all
costs and benefits of available regulatory alternatives and, if
regulation is necessary, to select regulatory approaches that maximize
net benefits (including potential economic, environmental, public
health and safety effects, distributive impacts, and equity). Executive
Order 13563 emphasizes the importance of quantifying both costs and
benefits, of reducing costs, of harmonizing rules, and of promoting
flexibility. This rule has been designated a ``significant regulatory
action'' although not economically significant, under section 3(f) of
Executive Order 12866. Accordingly, the rule has been reviewed by the
Office of Management and Budget.
2. Notwithstanding any other provision of law, no person is
required to respond to, nor shall any person be subject to a penalty
for failure to comply with, a collection of information subject to the
requirements of the Paperwork Reduction Act of 1995 (44 U.S.C. 3501 et
seq.) (PRA), unless that collection of information displays a currently
valid Office of Management and Budget (OMB) Control Number. This rule
contains a collection of information subject to the requirements of the
PRA. This collection has been approved by OMB under Control Number
0694-0088 (Multi-Purpose Application), which carries a burden hour
estimate of 58 minutes to prepare and submit form BIS-748. Send
comments regarding this burden estimate or any other aspect of this
collection of information, including suggestions for reducing the
burden, to Jasmeet Seehra, Office of Management and Budget (OMB), and
to the Regulatory Policy Division, Bureau of Industry and Security,
Department of Commerce, as indicated in the ADDRESSES section of this
rule.
3. This rule does not contain policies with Federalism implications
as that term is defined in Executive Order 13132.
4. The provisions of the Administrative Procedure Act (5 U.S.C.
553) requiring notice of proposed rulemaking, the opportunity for
public participation, and a delay in effective date, are inapplicable
because this regulation involves a military and foreign affairs
function of the United States (See 5 U.S.C. 553(a)(1)). Immediate
implementation of these amendments is non-discretionary and fulfills
the United States' international obligation to the Australia Group
(AG). The AG contributes to international security and regional
stability through the harmonization of export controls and seeks to
ensure that exports do not contribute to the development of chemical
and biological weapons. The AG consists of 40 member countries that act
on a consensus basis and the amendments set forth in this rule
implement the understandings reached at the June 2012 AG plenary
meeting, the 2012 AG intersessional changes, and other changes that are
necessary to ensure consistency with the controls maintained by the AG.
Since the United States is a significant exporter of the items in this
rule, immediate implementation of this provision is necessary for the
AG to achieve its purpose. Any delay in implementation will create a
disruption in the movement of affected items globally because of
disharmony between export control measures implemented by AG members,
resulting in tension between member countries. Export controls work
best when all countries implement the same export controls in a timely
and coordinated manner.
Further, no other law requires that a notice of proposed rulemaking
and an opportunity for public comment be given for this final rule.
Because a notice of proposed rulemaking and an opportunity for public
comment are not required to be given for this rule under the
Administrative Procedure Act or by any other law, the analytical
requirements of the Regulatory Flexibility Act (5 U.S.C. 601 et seq.)
are not applicable. Therefore, this regulation is issued in final form.
List of Subjects
15 CFR Part 740
Administrative practice and procedure, Exports, Reporting and
recordkeeping requirements.
15 CFR Part 742
Exports, Terrorism.
15 CFR Part 774
Exports, Reporting and recordkeeping requirements.
For the reasons stated in the preamble, parts 740, 742, and 774 of
the Export Administration Regulations (15 CFR parts 730-774) are
amended as follows:
PART 740--[AMENDED]
0
1. The authority citation for 15 CFR Part 740 continues to read as
follows:
Authority: 50 U.S.C. app. 2401 et seq.; 50 U.S.C. 1701 et seq.;
22 U.S.C. 7201 et seq.; E.O. 13026, 61 FR 58767, 3 CFR, 1996 Comp.,
p. 228; E.O. 13222, 66 FR 44025, 3 CFR, 2001 Comp., p. 783; Notice
of August 15, 2012, 77 FR 49699 (August 16, 2012).
0
2. Section 740.20 is amended by revising paragraph (b)(2)(v) to read as
follows:
[[Page 33696]]
Sec. 740.20 License Exception Strategic Trade Authorization (STA).
* * * * *
(b) * * *
(2) * * *
(v) License Exception STA may not be used for any item controlled
by ECCN 1C351.a, .b, .c, d.11, .d.12 or .e, ECCNs 1C352, 1C353, 1C354,
1E001 (i.e., for technology, as specified in ECCN 1E001, for items
controlled by ECCN 1C351.a, .b, .c, .d.11, .d.12 or .e or ECCNs 1C352,
1C353, or 1C354) or ECCN 1E351.
* * * * *
PART 742--[AMENDED]
0
3. The authority citation for 15 CFR Part 742 continues to read as
follows:
Authority: 50 U.S.C. app. 2401 et seq.; 50 U.S.C. 1701 et seq.;
22 U.S.C. 3201 et seq.; 42 U.S.C. 2139a; 22 U.S.C. 7201 et seq.; 22
U.S.C. 7210; Sec 1503, Pub. L. 108-11, 117 Stat. 559; E.O. 12058, 43
FR 20947, 3 CFR, 1978 Comp., p. 179; E.O. 12851, 58 FR 33181, 3 CFR,
1993 Comp., p. 608; E.O. 12938, 59 FR 59099, 3 CFR, 1994 Comp., p.
950; E.O. 13026, 61 FR 58767, 3 CFR, 1996 Comp., p. 228; E.O. 13222,
66 FR 44025, 3 CFR, 2001 Comp., p. 783; Presidential Determination
2003-23 of May 7, 2003, 68 FR 26459, May 16, 2003; Notice of August
15, 2012, 77 FR 49699 (August 16, 2012); Notice of November 9, 2011,
76 FR 70319 (November 10, 2011).
Sec. 742.2 [Amended]
0
4. Section 742.2 is amended by removing the phrase ``ECCNs 1C351,
1C352, 1C353, 1C354, and 1C360'' in paragraph (a)(1)(i) and adding in
its place the phrase ``ECCNs 1C351, 1C352, 1C353, and 1C354''.
PART 774--[AMENDED]
0
5. The authority citation for 15 CFR Part 774 continues to read as
follows:
Authority: 50 U.S.C. app. 2401 et seq.; 50 U.S.C. 1701 et seq.;
10 U.S.C. 7420; 10 U.S.C. 7430(e); 22 U.S.C. 287c, 22 U.S.C. 3201 et
seq., 22 U.S.C. 6004; 30 U.S.C. 185(s), 185(u); 42 U.S.C. 2139a; 42
U.S.C. 6212; 43 U.S.C. 1354; 15 U.S.C. 1824a; 50 U.S.C. app. 5; 22
U.S.C. 7201 et seq.; 22 U.S.C. 7210; E.O. 13026, 61 FR 58767, 3 CFR,
1996 Comp., p. 228; E.O. 13222, 66 FR 44025, 3 CFR, 2001 Comp., p.
783; Notice of August 15, 2012, 77 FR 49699 (August 16, 2012).
Supplement No. 1 to Part 774--[Amended]
0
6. In Supplement No. 1 to Part 774 (the Commerce Control List),
Category 1--Special Materials and Related Equipment, Chemicals,
``Microorganisms'' and ``Toxins,'' ECCN 1C351 is amended by adding a
new Note 4 in the ``License Requirements Notes'' under the License
Requirements section, by revising the ``Related Controls'' paragraph
under the List of Items Controlled section, and, in the ``Items''
paragraph under the List of Items Controlled section, by revising the
heading of paragraph a., by revising paragraph a.35, by adding a new
paragraph b., by revising paragraph c., by revising the heading of
paragraph d., and by revising paragraph d.14 to read as follows:
1C351 Human and zoonotic pathogens and ``toxins'', as follows (see
List of Items Controlled).
License Requirements
* * * * *
License Requirement Notes: * * *
4. Unless specified elsewhere in this ECCN 1C351 (e.g., in
License Requirement Notes 1-3), this ECCN controls all biological
agents and ``toxins,'' regardless of quantity or attenuation, that
are identified in the List of Items Controlled for this ECCN,
including small quantities or attenuated strains of select
biological agents or ``toxins'' that are excluded from the lists of
select biological agents or ``toxins'' by the Animal and Plant
Health Inspection Service (APHIS), U.S. Department of Agriculture,
or the Centers for Disease Control and Prevention (CDC), U.S.
Department of Health and Human Services, in accordance with their
regulations in 9 CFR part 121 and 42 CFR part 73, respectively.
* * * * *
List of Items Controlled
Unit: * * *
Related Controls: (1) Certain forms of ricin and saxitoxin in
1C351.d.11. and d.12 are CWC Schedule 1 chemicals (see Sec. 742.18
of the EAR). The U.S. Government must provide advance notification
and annual reports to the OPCW of all exports of Schedule 1
chemicals. See Sec. 745.1 of the EAR for notification procedures.
See 22 CFR part 121, Category XIV and Sec. 121.7 for CWC Schedule 1
chemicals that are subject to the export licensing jurisdiction of
the U.S. Department of State, Directorate of Defense Trade Controls.
(2) The Animal and Plant Health Inspection Service (APHIS), U.S.
Department of Agriculture, and the Centers for Disease Control and
Prevention (CDC), U.S. Department of Health and Human Services,
maintain controls on the possession, use, and transfer within the
United States of certain items controlled by this ECCN (for APHIS,
see 7 CFR 331.3(b), 9 CFR 121.3(b), and 9 CFR 121.4(b); for CDC, see
42 CFR 73.3(b) and 42 CFR 73.4(b)). (3) See 22 CFR part 121,
Category XIV(b), for modified biological agents and biologically
derived substances that are subject to the export licensing
jurisdiction of the U.S. Department of State, Directorate of Defense
Trade Controls.
Related Definitions: * * *
Items:
a. Viruses identified on the Australia Group (AG) ``List of
Biological Agents for Export Control,'' as follows:
* * * * *
a.35. Tick-borne encephalitis virus (Far Eastern subtype,
formerly known as Russian Spring-Summer encephalitis virus--see
1C351.b.3 for Siberian subtype);
* * * * *
b. Viruses identified on the APHIS/CDC ``select agents'' lists
(see Related Controls paragraph 2 for this ECCN), but not
identified on the Australia Group (AG) ``List of Biological Agents
for Export Control,'' as follows:
b.1. Reconstructed replication competent forms of the 1918
pandemic influenza virus containing any portion of the coding
regions of all eight gene segments;
b.2. SARS-associated coronavirus (SARS-CoV); or
b.3. Tick-borne encephalitis virus (Siberian subtype, formerly
West Siberian virus--see 1C351.a.35 for Far Eastern subtype).
c. Bacteria identified on the Australia Group (AG) ``List of
Biological Agents for Export Control,'' as follows:
c.1. Bacillus anthracis;
c.2. Brucella abortus;
c.3. Brucella melitensis;
c.4. Brucella suis;
c.5. Burkholderia mallei (Pseudomonas mallei);
c.6. Burkholderia pseudomallei (Pseudomonas pseudomallei);
c.7. Chlamydophila psittaci (formerly known as Chlamydia
psittaci);
c.8. Clostriduim argentinense (formerly known as Clostridium
botulinum Type G), botulinum neurotoxin producing strains;
c.9. Clostridium baratii, botulinum neurotoxin producing
strains;
c.10. Clostridium botulinum;
c.11. Clostridium butyricum, botulinum neurotoxin producing
strains;
c.12. Clostridium perfringens, epsilon toxin producing types;
c.13. Coxiella burnetii;
c.14. Francisella tularensis;
c.15. Rickettsia prowazekii;
c.16. Salmonella typhi;
c.17. Shiga toxin producing Escherichia coli (STEC) of
serogroups O26, O45, O103, O104, O111, O121, O145, O157, and other
shiga toxin producing serogroups;
Note: Shiga toxin producing Escherichia coli (STEC) is also
known as enterohaemorrhagic E. coli (EHEC) or verocytotoxin
producing E. coli (VTEC).
c.18. Shigella dysenteriae;
c.19. Vibrio cholerae; or
c.20. Yersinia pestis.
d. ``Toxins'' identified on the Australia Group (AG) ``List of
Biological Agents for Export Control,'' as follows, and ``subunits''
thereof:
* * * * *
d.14. Staphylococcus aureus enterotoxins, hemolysin alpha toxin,
and toxic shock syndrome toxin (formerly known as Staphylococcus
enterotoxin F);
* * * * *
0
7. In Supplement No. 1 to Part 774 (the Commerce Control List),
Category 1-- Special Materials and Related Equipment, Chemicals,
``Microorganisms'' and ``Toxins,'' ECCN 1C352 is amended by revising
the ``License Requirement Note'' under the License Requirements section
and by
[[Page 33697]]
revising the ``Related Controls'' paragraph under the List of Items
Controlled section to read as follows:
1C352 Animal pathogens, as follows (see List of Items Controlled).
License Requirements
* * * * *
License Requirements Notes:
1. All vaccines are excluded from the scope of this ECCN. See
ECCN 1C991 for vaccines.
2. Unless specified elsewhere in this ECCN 1C352 (e.g., in
License Requirement Note 1), this ECCN controls all biological
agents, regardless of quantity or attenuation, that are identified
in the List of Items Controlled for this ECCN, including small
quantities or attenuated strains of select biological agents that
are excluded from the lists of select biological agents or
``toxins'' by the Animal and Plant Health Inspection Service
(APHIS), U.S. Department of Agriculture, or the Centers for Disease
Control and Prevention (CDC), U.S. Department of Health and Human
Services, in accordance with their regulations in 9 CFR part 121 and
42 CFR part 73, respectively.
* * * * *
List of Items Controlled
Unit: * * *
Related Controls: (1) The Animal and Plant Health Inspection Service
(APHIS), U.S. Department of Agriculture, and the Centers for Disease
Control and Prevention (CDC), U.S. Department of Health and Human
Services, maintain controls on the possession, use, and transfer
within the United States of certain items controlled by this ECCN
(for APHIS, see 7 CFR 331.3(b), 9 CFR 121.3(b), and 9 CFR 121.4(b);
for CDC, see 42 CFR 73.3(b) and 42 CFR 73.4(b)). (2) See 22 CFR part
121, Category XIV(b), for modified biological agents and
biologically derived substances that are subject to the export
licensing jurisdiction of the U.S. Department of State, Directorate
of Defense Trade Controls.
Related Definitions: * * *
Items:
* * * * *
0
8. In Supplement No. 1 to Part 774 (the Commerce Control List),
Category 1-- Special Materials and Related Equipment, Chemicals,
``Microorganisms'' and ``Toxins,'' ECCN 1C353 is amended, under the
License Requirements section, by revising the ``License Requirements
Note'' and, under the List of Items Controlled section, by revising the
``Related Controls'' paragraph, by revising paragraphs a.1. and b.1. in
the ``Items'' paragraph, and by revising Technical Note 3, to read as
follows:
1C353 Genetic elements and genetically modified organisms, as
follows (see List of Items Controlled).
License Requirements
* * * * *
License Requirements Notes:
1. Vaccines that contain genetic elements or genetically
modified organisms identified in this ECCN are controlled by ECCN
1C991.
2. Unless specified elsewhere in this ECCN 1C353 (e.g., in
License Requirement Note 1), this ECCN controls genetic elements or
genetically modified organisms for all biological agents and
``toxins,'' regardless of quantity or attenuation, that are
identified in the List of Items Controlled for this ECCN, including
genetic elements or genetically modified organisms for attenuated
strains of select biological agents or ``toxins'' that are excluded
from the lists of select biological agents or ``toxins'' by the
Animal and Plant Health Inspection Service (APHIS), U.S. Department
of Agriculture, or the Centers for Disease Control and Prevention
(CDC), U.S. Department of Health and Human Services, in accordance
with the APHIS regulations in 7 CFR part 331 and 9 CFR part 121 and
the CDC regulations in 42 CFR part 73.
* * * * *
List of Items Controlled
Unit: * * *
Related Controls: (1) The Animal and Plant Health Inspection Service
(APHIS), U.S. Department of Agriculture, and the Centers for Disease
Control and Prevention (CDC), U.S. Department of Health and Human
Services, maintain controls on the possession, use, and transfer
within the United States of certain items controlled by this ECCN,
including (but not limited to) certain genetic elements, recombinant
nucleic acids, and recombinant organisms associated with the agents
or toxins in ECCN 1C351, 1C352, or 1C354 (for APHIS, see 7 CFR
331.3(c), 9 CFR 121.3(c), and 9 CFR 121.4(c); for CDC, see 42 CFR
73.3(c) and 42 CFR 73.4(c)). (2) See 22 CFR part 121, Category
XIV(b), for modified biological agents and biologically derived
substances that are subject to the export licensing jurisdiction of
the U.S. Department of State, Directorate of Defense Trade Controls.
Related Definition: * * *
Items:
a. * * *
a.1. Genetic elements that contain nucleic acid sequences
associated with the pathogenicity of microorganisms controlled by
1C351.a to .c, 1C352, or 1C354;
a.2. * * *
b. * * *
b.1. Genetically modified organisms that contain nucleic acid
sequences associated with the pathogenicity of microorganisms
controlled by 1C351.a to .c, 1C352, or 1C354;
b.2. * * *
Technical Notes:
* * * * *
3. ``Nucleic acid sequences associated with the pathogenicity of
any of the microorganisms controlled by 1C351.a to .c, 1C352, or
1C354'' means any sequence specific to the relevant controlled
microorganism that:
a. In itself or through its transcribed or translated products
represents a significant hazard to human, animal or plant health; or
b. Is known to enhance the ability of a microorganism controlled
by 1C351.a to .c, 1C352, or 1C354, or any other organism into which
it may be inserted or otherwise integrated, to cause serious harm to
human, animal or plant health.
* * * * *
0
9. In Supplement No. 1 to Part 774 (the Commerce Control List),
Category 1--Special Materials and Related Equipment, Chemicals,
``Microorganisms'' and ``Toxins,'' ECCN 1C354 is amended by revising
the ``License Requirements Note'' under the License Requirements
section and by revising the ``Related Controls'' paragraph and the
``Items'' paragraph under the List of Items Controlled section to read
as follows:
1C354 Plant pathogens, as follows (see List of Items Controlled).
License Requirements
* * * * *
License Requirements Notes:
1. All vaccines are excluded from the scope of this ECCN. See
ECCN 1C991 for vaccines.
2. Unless specified elsewhere in this ECCN 1C354 (e.g., in
License Requirement Note 1), this ECCN controls all biological
agents, regardless of quantity or attenuation, that are identified
in the List of Items Controlled for this ECCN, including small
quantities or attenuated strains of select biological agents that
are excluded from the list of PPQ select agents and ``toxins'' by
the Animal and Plant Health Inspection Service (APHIS), U.S.
Department of Agriculture, in accordance with their regulations in 7
CFR part 331.
* * * * *
List of Items Controlled
Unit: * * *
Related Controls: (1) The Animal and Plant Health Inspection Service
(APHIS), U.S. Department of Agriculture, maintains controls on the
possession, use, and transfer within the United States of certain
items controlled by this ECCN (see 7 CFR 331.3(c), 9 CFR 121.3(c),
and 9 CFR 121.4(c)). (2) See 22 CFR part 121, Category XIV(b), for
modified biological agents and biologically derived substances that
are subject to the export licensing jurisdiction of the U.S.
Department of State, Directorate of Defense Trade Controls.
Related Definition: * * *
Items:
a. Bacteria, as follows:
a.1. Xanthomonas albilineans;
a.2. Xanthomonas axonopodis pv. citri (Xanthomonas campestris
pv. citri A) (Xanthomonas campestris pv. citri);
a.3. Xanthomonas oryzae [this species of proteobacteria is
identified on the APHIS ``select agents'' list (see Related Controls
paragraph for this ECCN), but only the pathovar Xanthomonas oryzae
pv. oryzae (syn. Pseudomonas campestris pv. oryzae) is identified on
the Australia Group (AG) ``List of Plant Pathogens for Export
Control''];
a.4. Clavibacter michiganensis subspecies sepedonicus (syn.
Corynebacterium michiganensis subspecies sepedonicum or
Corynebacterium sepedonicum);
[[Page 33698]]
a.5. Ralstonia solanacearum, race 3, biovar 2;
a.6. Raythayibactor toxicus [this bacterium is identified on the
APHIS ``select agents'' list (see the Related Controls paragraph for
this ECCN), but is not identified on the Australia Group (AG) ``List
of Plant Pathogens for Export Control''].
b. Fungi, as follows:
b.1. Colletotrichum kahawae (Colletotrichum coffeanum var.
virulans);
b.2. Cochliobolus miyabeanus (Helminthosporium oryzae);
b.3. Microcyclus ulei (syn. Dothidella ulei);
b.4. Puccinnia graminis ssp. graminis var. graminis/Puccinia
graminis ssp. graminis var. stakmanii (Puccinia graminis [syn.
Puccinia graminis f. sp. tritici]);
b.5. Puccinia striiformis (syn. Puccinia glumarum);
b.6. Magnaporthe oryzae (Pyricularia oryzae);
b.7. Peronosclerospora philippinensis (Peronosclerospora
sacchari);
b.8. Sclerophthora rayssiae var. zeae;
b.9. Synchytrium endobioticum;
b.10. Tilletia indica;
b.11. Thecaphora solani;
b.12. Phoma glycinicola (formerly Pyrenochaeta glycines) [this
fungus is identified on the APHIS ``select agents'' list (see the
Related Controls paragraph for this ECCN), but is not identified on
the Australia Group (AG) ``List of Plant Pathogens for Export
Control''].
c. Viruses, as follows:
c.1. Andean potato latent virus (Potato Andean latent
tymovirus);
c.2. Potato spindle tuber viroid.
0
10. In Supplement No. 1 to Part 774 (the Commerce Control List),
Category 1--Special Materials and Related Equipment, Chemicals,
``Microorganisms'' and ``Toxins,'' ECCN 1C360 is removed.
0
11. In Supplement No. 1 to Part 774 (the Commerce Control List),
Category 1--Special Materials and Related Equipment, Chemicals,
``Microorganisms'' and ``Toxins,'' ECCN 1C991 is amended under the List
of Items Controlled section by revising the fourth sentence in the
``Related Definitions'' paragraph and by revising paragraph a. in the
``Items'' paragraph to read as follows:
1C991 Vaccines, immunotoxins, medical products, diagnostic and food
testing kits, as follows (see List of Items Controlled).
* * * * *
List of Items Controlled
Unit: * * *
Related Controls: * * *
Related Definitions: * * * Biological toxins in any other
configuration, including bulk shipments, or for any other end-uses
are controlled by ECCN 1C351. * * *
Items:
a. Vaccines against items controlled by ECCN 1C351, 1C352, 1C353
or 1C354.
* * * * *
0
12. In Supplement No. 1 to Part 774 (the Commerce Control List),
Category 1--Special Materials and Related Equipment, Chemicals,
``Microorganisms'' and ``Toxins,'' ECCN 1E001 is amended by revising
the ECCN heading and by revising the ``Control(s)'' language for
``Country Chart--CB Column 1'' in the License Requirements section to
read as follows:
1E001 ``Technology'' according to the General Technology Note for
the ``Development'' or ``Production'' of items controlled by
1A001.b, 1A001.c, 1A002, 1A003, 1A004, 1A005, 1A006.b, 1A007, 1A008,
1A101, 1B (except 1B999), or 1C (except 1C355, 1C980 to 1C984,
1C988, 1C990, 1C991, 1C995 to 1C999).
License Requirements
Reason for Control: NS, MT, NP, CB, RS, AT
Control(s) Country chart
* * * * *
CB applies to ``technology'' for items CB Column 1.
controlled by 1C351, 1C352, 1C353, or
1C354.
* * * * *
License Requirements Note: * * *
* * * * *
0
13. In Supplement No. 1 to Part 774 (the Commerce Control List),
Category 1--Special Materials and Related Equipment, Chemicals,
``Microorganisms'' and ``Toxins,'' ECCN 1E351 is amended by revising
the ECCN heading and by revising the ``Control(s)'' language for
``Country Chart--CB Column 1'' in the License Requirements section to
read as follows:
1E351 ``Technology'' according to the ``General Technology Note'' for
the disposal of chemicals or microbiological materials controlled by
1C350, 1C351, 1C352, 1C353, or 1C354.
License Requirements
Reason for Control: CB, AT
Control(s) Country chart
CB applies to ``technology'' for the CB Column 1.
disposal of items controlled by 1C351,
1C352, 1C353, or 1C354.
* * * * *
* * * * *
0
14. In Supplement No. 1 to Part 774 (the Commerce Control List),
Category 2--Materials Processing, ECCN 2B352 is amended under the
``Items'' paragraph in the List of Items Controlled section by
redesignating paragraphs f. through h. as paragraphs g. through i.,
respectively, and adding a new paragraph f. to read as follows:
2B352 Equipment capable of use in handling biological materials, as
follows (see List of Items Controlled).
* * * * *
List of Items Controlled
Unit: * * *
Related Controls: * * *
Related Definitions: * * *
Items:
* * * * *
f. Spray-drying equipment capable of drying toxins or pathogenic
microorganisms having all of the flowing characteristics:
f.1. A water evaporation capacity of >= 0.4 kg/h and <= 400 kg/
h;
f.2. The ability to generate a typical mean product particle
size of <= 10 micrometers with existing fittings or by minimal
modification of the spray-dryer with atomization nozzles enabling
generation of the required particle size; and
f.3. Capable of being sterilized or disinfected in situ.
* * * * *
Dated: May 29, 2013.
Kevin J. Wolf,
Assistant Secretary for Export Administration.
[FR Doc. 2013-13270 Filed 6-4-13; 8:45 am]
BILLING CODE 3510-33-P