Approval of Test Marketing Exemption for a Certain New Microorganism, 29319-29320 [E7-10067]
Download as PDF
Federal Register / Vol. 72, No. 101 / Friday, May 25, 2007 / Notices
List of Subjects
Environmental protection, Hazardous
substances, Polychlorinated biphenyls
(PCBs), Reporting and recordkeeping
requirements.
Dated: May 21, 2007.
Wendy C. Hamnett,
Acting Director, Office of Pollution Prevention
and Toxics.
[FR Doc. E7–10117 Filed 5–24–07; 8:45 am]
BILLING CODE 6560–50–S
ENVIRONMENTAL PROTECTION
AGENCY
[EPA–HQ–OPPT–2007–1019; FRL–8119–9]
Approval of Test Marketing Exemption
for a Certain New Microorganism
Environmental Protection
Agency (EPA).
ACTION: Notice.
AGENCY:
SUMMARY: This notice announces EPA’s
approval of an application for test
marketing exemption (TME) under
section 5(h)(1) of the Toxic Substances
Control Act (TSCA) and 40 CFR part
725, subpart F. EPA has designated this
application as TME–06–09. The test
marketing conditions are described in
the TME application and in this notice.
DATES: Approval of this TME became
effective December 21, 2006.
FOR FURTHER INFORMATION CONTACT: For
general information contact: Colby
Lintner, Regulatory Coordinator,
Environmental Assistance Division
(7408M), Office of Pollution Prevention
and Toxics, Environmental Protection
Agency, 1200 Pennsylvania Ave., NW.,
Washington, DC 20460–0001; telephone
number: (202) 554–1404; e-mail address:
TSCA-Hotline@epa.gov.
For technical information contact:
Audrey Binder, Chemical Control
Division (7405M), Office of Pollution
Prevention and Toxics, Environmental
Protection Agency, 1200 Pennsylvania
Ave., NW., Washington, DC 20460–
0001; telephone number: (202) 564–
9033; e-mail address:
binder.audrey@epa.gov.
SUPPLEMENTARY INFORMATION:
jlentini on PROD1PC65 with NOTICES
I. General Information
A. Does this Action Apply to Me?
This action is directed in particular to
the microorganism manufacturer who
submitted the TME to EPA. This action
may, however, be of interest to the
public in general. Since other entities
may also be interested, the Agency has
not attempted to describe all the specific
entities that may be affected by this
action. If you have any questions
VerDate Aug<31>2005
17:34 May 24, 2007
Jkt 211001
regarding the applicability of this action
to a particular entity, consult the
technical person listed under FOR
FURTHER INFORMATION CONTACT.
B. How Can I get Copies of this
Document and Other Related
Information?
1. Docket. EPA has established a
docket for this action under docket ID
number EPA–HQ–OPPT–2007–1019.
All documents in the docket are listed
in the docket’s index at https://
www.regulations.gov. Although listed in
the index, some information is not
publicly available, e.g., Confidential
Business Information (CBI) or other
information whose disclosure is
restricted by statute. Certain other
material, such as copyrighted material,
will be publicly available only in hard
copy. Publicly available docket
materials are available electronically at
https://www.regulations.gov, or, if only
available in hard copy, at the OPPT
Docket. The OPPT Docket is located in
the EPA Docket Center (EPA/DC) at Rm.
3334, EPA West Bldg., 1301
Constitution Ave., NW., Washington,
DC. The EPA/DC Public Reading Room
hours of operation are 8:30 a.m. to 4:30
p.m., Monday through Friday, excluding
Federal holidays. The telephone number
of the EPA/DC Public Reading Room is
(202) 566–1744, and the telephone
number for the OPPT Docket is (202)
566–0280. Docket visitors are required
to show photographic identification,
pass through a metal detector, and sign
the EPA visitor log. All visitor bags are
processed through an X-ray machine
and subject to search. Visitors will be
provided an EPA/DC badge that must be
visible at all times in the building and
returned upon departure.
2. Electronic access. You may access
this Federal Register document
electronically through the EPA Internet
under the ‘‘Federal Register’’ listings at
https://www.epa.gov/fedrgstr.
II. What is the Agency’s Authority for
Taking this Action?
Section 5(h)(1) of TSCA and 40 CFR
part 725, subpart F authorizes EPA to
exempt persons from Microbial
Commercial Activity Notification
(MCAN) requirements and permit them
to manufacture or import new
microorganisms for test marketing
purposes, if the Agency finds that the
manufacture, processing, distribution in
commerce, use, and disposal of the
microorganisms for test marketing
purposes will not present an
unreasonable risk of injury to health or
the environment. EPA may impose
restrictions on test marketing activities
and may modify or revoke a test
PO 00000
Frm 00027
Fmt 4703
Sfmt 4703
29319
marketing exemption upon receipt of
new information which casts significant
doubt on its finding that the test
marketing activity will not present an
unreasonable risk of injury.
III. What Action is the Agency Taking?
EPA has approved the abovereferenced TME. EPA has determined
that test marketing the new
microorganism, under the conditions set
out in the TME application and in this
notice, will not present any
unreasonable risk of injury to health or
the environment.
IV. What Restrictions Apply to this
TME?
The test market time period,
production volume, and use must not
exceed specifications in the application
and this notice. All other conditions and
restrictions described in the application
and in this notice must also be met.
Impacts to the environment must also be
managed as described in the TME as
amended.
TME–06–09.
Date of Receipt: September 14, 2006.
Notice of Receipt: October 13, 2006
(71 FR 60517) (FRL–8099–3).
Applicant: Confidential.
Microorganism: Organic acid
producing organism.
Use: Industrial manufacture of an
organic acid.
Production Volume: Confidential.
Number of Customers: Confidential.
Test Marketing Period: Duration as
specified in TME application,
commencing on first day of commercial
manufacture.
The following additional restrictions
apply to this TME. A bill of lading
accompanying each shipment must state
that the use of the microorganism is
restricted to that approved in the TME.
In addition, the applicant shall maintain
the following records until 5 years after
the date they are created, and shall
make them available for inspection or
copying in accordance with section 11
of TSCA:
1. Records of the quantity of the TME
microorganism produced and the date of
manufacture.
2. Records of dates of the shipments
to each customer and the quantities
supplied in each shipment.
3. Copies of the bill of lading that
accompanies each shipment of the TME
microorganism.
V. What was EPA’s Risk Assessment for
this TME?
Under the conditions required for this
TME, EPA identified no significant
health or environmental concerns for
E:\FR\FM\25MYN1.SGM
25MYN1
29320
Federal Register / Vol. 72, No. 101 / Friday, May 25, 2007 / Notices
the test market microorganism.
Therefore, the test market activities will
not present any unreasonable risk of
injury to human health or the
environment.
VI. Can EPA Change Its Decision on this
TME in the Future?
Yes. The Agency reserves the right to
rescind approval or modify the
conditions and restrictions of an
exemption should any new information
that comes to its attention cast
significant doubt on its finding that the
test marketing activities will not present
any unreasonable risk of injury to
human health or the environment.
List of Subjects
Environmental protection, Test
marketing exemptions.
Dated: March 15, 2007.
Rebecca S. Cool,
Chief, New Chemicals Notice Management
Branch, Office of Pollution Prevention and
Toxics.
[FR Doc. E7–10067 Filed 5–24–07; 8:45 am]
BILLING CODE 6560–50–S
ENVIRONMENTAL PROTECTION
AGENCY
[FRL–8318–4]
Underground Injection Control
Program Petition for Exemption From
Hazardous Waste Disposal
Restrictions to the Resource
Conservation and Recovery Act Class
I Hazardous Waste Injection Occidental
Chemical Corporation, Wichita, KS
Environmental Protection
Agency (EPA).
ACTION: Notice of final decision on
petition.
jlentini on PROD1PC65 with NOTICES
AGENCY:
SUMMARY: Notice is hereby given that an
exemption to the land disposal
restrictions under the 1984 Hazardous
and Solid Waste Amendments to the
Resource Conservation and Recovery
Act has been granted to Occidental
Chemical Corporation (Occidental) for a
Class I injection well, identified as Well
Number 10, located at Wichita, Kansas.
This injection well, is being added to an
existing group of five hazardous waste
injection wells which EPA had
approved in 1990. As required by title
40 Code of Federal Regulations (CFR)
part 148, Occidental has adequately
demonstrated to the satisfaction of the
Environmental Protection Agency by
petition and supporting documentation
that, to a reasonable degree of certainty,
there will be no migration of hazardous
waste out of the designated injection
zone for as long as the waste remains
VerDate Aug<31>2005
17:34 May 24, 2007
Jkt 211001
hazardous. This time frame is defined
by 40 CFR 148.20 as 10,000 years. This
final decision allows the underground
injection by Occidental of the specific
restricted waste, identified in the
petition, into injection well Number 10
at the Wichita, Kansas facility, for as
long as the basis for granting an
approval of the petition remains valid,
under provisions of 40 CFR 148.24. For
the purpose of the required
demonstration of no-migration of
hazardous waste out of the injection
zone over a 10,000 year period,
modeling and projections were based on
an operational lifetime projection date
of December 31, 2020. Therefore, on or
by the closing date of the
aforementioned operation period, the
owner/operator will be required to
obtain an exemption re-issuance from
EPA. Included in this approval is the
stipulation that Occidental acquires and
continues to maintain an approved
permit from the Kansas Department of
Health and Environment. As required by
40 CFR 124.10, a public notice was
issued on February 26, 2007. In addition
to having solicited written comments
regarding the Agency’s proposed
approval, EPA also announced that a
formal public hearing would be held if
there was a significant degree of public
interest, but no interest was expressed,
hence no formal public hearing was
conducted; however, EPA held an
informal Public Availability Session on
March 13, 2007, at the Sedgwick County
Extension Office in Wichita, Kansas, in
order to provide the public with an
opportunity to meet with Federal, State,
and company officials and ask questions
regarding the petition. The public
comment period ended on April 11,
2007. All comments were addressed and
considered in the final decision. This
decision constitutes final Agency action
and there is no administrative appeal
process that can be applied to a final
petition decision.
Effective Date: This action is
effective as of May 2, 2007.
DATES:
Copies of the petition and
all pertinent information relating
thereto, including the Agency’s
response to comments, are on file at the
following location: Environmental
Protection Agency, Region 7, Regional
Records Center, 901 N. 5th St., Kansas
City, KS 66101.
ADDRESSES:
FOR FURTHER INFORMATION CONTACT:
Mary T. Mindrup, Chief, Drinking Water
Management Branch, Environmental
Protection Agency, Region 7. Telephone
(913) 551–7431, or e-mail to
mindrup.mary@epa.gov.
PO 00000
Frm 00028
Fmt 4703
Sfmt 4703
Dated: May 2, 2007.
John B. Askew,
Regional Administrator, Region 7.
[FR Doc. E7–10118 Filed 5–24–07; 8:45 am]
BILLING CODE 6560–50–P
FEDERAL ACCOUNTING STANDARDS
ADVISORY BOARD
Notice of New Exposure Draft
Accounting for Federal Oil and Gas
Resources
Federal Accounting Standard
Advisory Board.
AGENCY:
Notice of new exposure draft
Accounting for Federal Oil and Gas
Resources.
ACTION:
Board Action: Pursuant to 31 U.S.C.
3511(d), the Federal Advisory
Committee Act (Pub. L. 92–463), as
amended, and the FASAB Rules Of
Procedure, as amended in April 2004,
notice is hereby given that the Federal
Accounting Standards Advisory Board
(FASAB) has issued an exposure draft,
Accounting for Federal Oil and Gas
Resources.
The Exposure Draft proposes
standards that would result in
recognition of the estimated value of
royalties from Federal oil and gas leases
and changes in those values over time
as well as the amount of royalties
designated for distribution to other
entities such as State governments.
The Exposure Draft is available on the
FASAB home page https://
www.fasab.gov/exposure.html. Copies
can be obtained by contacting FASAB at
(202) 512–7350. Respondents are
encouraged to comment on any part of
the exposure draft. Written comments
are requested by September 21, 2007,
and should be sent to: Wendy M.
Comes, Executive Director, Federal
Accounting Standards Advisory Board,
441 G Street, NW., Suite 6814, Mail
Stop 6K17V, Washington, DC 20548.
FOR FURTHER INFORMATION CONTACT:
Wendy Comes, Executive Director, 441
G Street, NW., Washington, DC 20548,
or call (202) 512–7350.
Authority: Federal Advisory Committee
Act, Pub. L. No. 92–463.
Dated: May 22, 2007.
Charles Jackson,
Federal Register Liaison Officer.
[FR Doc. 07–2606 Filed 5–24–07; 8:45 am]
BILLING CODE 1610–01–M
E:\FR\FM\25MYN1.SGM
25MYN1
Agencies
[Federal Register Volume 72, Number 101 (Friday, May 25, 2007)]
[Notices]
[Pages 29319-29320]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E7-10067]
-----------------------------------------------------------------------
ENVIRONMENTAL PROTECTION AGENCY
[EPA-HQ-OPPT-2007-1019; FRL-8119-9]
Approval of Test Marketing Exemption for a Certain New
Microorganism
AGENCY: Environmental Protection Agency (EPA).
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: This notice announces EPA's approval of an application for
test marketing exemption (TME) under section 5(h)(1) of the Toxic
Substances Control Act (TSCA) and 40 CFR part 725, subpart F. EPA has
designated this application as TME-06-09. The test marketing conditions
are described in the TME application and in this notice.
DATES: Approval of this TME became effective December 21, 2006.
FOR FURTHER INFORMATION CONTACT: For general information contact: Colby
Lintner, Regulatory Coordinator, Environmental Assistance Division
(7408M), Office of Pollution Prevention and Toxics, Environmental
Protection Agency, 1200 Pennsylvania Ave., NW., Washington, DC 20460-
0001; telephone number: (202) 554-1404; e-mail address: TSCA-
Hotline@epa.gov.
For technical information contact: Audrey Binder, Chemical Control
Division (7405M), Office of Pollution Prevention and Toxics,
Environmental Protection Agency, 1200 Pennsylvania Ave., NW.,
Washington, DC 20460-0001; telephone number: (202) 564-9033; e-mail
address: binder.audrey@epa.gov.
SUPPLEMENTARY INFORMATION:
I. General Information
A. Does this Action Apply to Me?
This action is directed in particular to the microorganism
manufacturer who submitted the TME to EPA. This action may, however, be
of interest to the public in general. Since other entities may also be
interested, the Agency has not attempted to describe all the specific
entities that may be affected by this action. If you have any questions
regarding the applicability of this action to a particular entity,
consult the technical person listed under FOR FURTHER INFORMATION
CONTACT.
B. How Can I get Copies of this Document and Other Related Information?
1. Docket. EPA has established a docket for this action under
docket ID number EPA-HQ-OPPT-2007-1019. All documents in the docket are
listed in the docket's index at https://www.regulations.gov. Although
listed in the index, some information is not publicly available, e.g.,
Confidential Business Information (CBI) or other information whose
disclosure is restricted by statute. Certain other material, such as
copyrighted material, will be publicly available only in hard copy.
Publicly available docket materials are available electronically at
https://www.regulations.gov, or, if only available in hard copy, at the
OPPT Docket. The OPPT Docket is located in the EPA Docket Center (EPA/
DC) at Rm. 3334, EPA West Bldg., 1301 Constitution Ave., NW.,
Washington, DC. The EPA/DC Public Reading Room hours of operation are
8:30 a.m. to 4:30 p.m., Monday through Friday, excluding Federal
holidays. The telephone number of the EPA/DC Public Reading Room is
(202) 566-1744, and the telephone number for the OPPT Docket is (202)
566-0280. Docket visitors are required to show photographic
identification, pass through a metal detector, and sign the EPA visitor
log. All visitor bags are processed through an X-ray machine and
subject to search. Visitors will be provided an EPA/DC badge that must
be visible at all times in the building and returned upon departure.
2. Electronic access. You may access this Federal Register document
electronically through the EPA Internet under the ``Federal Register''
listings at https://www.epa.gov/fedrgstr.
II. What is the Agency's Authority for Taking this Action?
Section 5(h)(1) of TSCA and 40 CFR part 725, subpart F authorizes
EPA to exempt persons from Microbial Commercial Activity Notification
(MCAN) requirements and permit them to manufacture or import new
microorganisms for test marketing purposes, if the Agency finds that
the manufacture, processing, distribution in commerce, use, and
disposal of the microorganisms for test marketing purposes will not
present an unreasonable risk of injury to health or the environment.
EPA may impose restrictions on test marketing activities and may modify
or revoke a test marketing exemption upon receipt of new information
which casts significant doubt on its finding that the test marketing
activity will not present an unreasonable risk of injury.
III. What Action is the Agency Taking?
EPA has approved the above-referenced TME. EPA has determined that
test marketing the new microorganism, under the conditions set out in
the TME application and in this notice, will not present any
unreasonable risk of injury to health or the environment.
IV. What Restrictions Apply to this TME?
The test market time period, production volume, and use must not
exceed specifications in the application and this notice. All other
conditions and restrictions described in the application and in this
notice must also be met. Impacts to the environment must also be
managed as described in the TME as amended.
TME-06-09.
Date of Receipt: September 14, 2006.
Notice of Receipt: October 13, 2006 (71 FR 60517) (FRL-8099-3).
Applicant: Confidential.
Microorganism: Organic acid producing organism.
Use: Industrial manufacture of an organic acid.
Production Volume: Confidential.
Number of Customers: Confidential.
Test Marketing Period: Duration as specified in TME application,
commencing on first day of commercial manufacture.
The following additional restrictions apply to this TME. A bill of
lading accompanying each shipment must state that the use of the
microorganism is restricted to that approved in the TME. In addition,
the applicant shall maintain the following records until 5 years after
the date they are created, and shall make them available for inspection
or copying in accordance with section 11 of TSCA:
1. Records of the quantity of the TME microorganism produced and
the date of manufacture.
2. Records of dates of the shipments to each customer and the
quantities supplied in each shipment.
3. Copies of the bill of lading that accompanies each shipment of
the TME microorganism.
V. What was EPA's Risk Assessment for this TME?
Under the conditions required for this TME, EPA identified no
significant health or environmental concerns for
[[Page 29320]]
the test market microorganism. Therefore, the test market activities
will not present any unreasonable risk of injury to human health or the
environment.
VI. Can EPA Change Its Decision on this TME in the Future?
Yes. The Agency reserves the right to rescind approval or modify
the conditions and restrictions of an exemption should any new
information that comes to its attention cast significant doubt on its
finding that the test marketing activities will not present any
unreasonable risk of injury to human health or the environment.
List of Subjects
Environmental protection, Test marketing exemptions.
Dated: March 15, 2007.
Rebecca S. Cool,
Chief, New Chemicals Notice Management Branch, Office of Pollution
Prevention and Toxics.
[FR Doc. E7-10067 Filed 5-24-07; 8:45 am]
BILLING CODE 6560-50-S