Sally Shaw; Denial of Petition for Rulemaking, 71083-71086 [E7-24291]
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Proposed Rules
Federal Register
Vol. 72, No. 240
Friday, December 14, 2007
This section of the FEDERAL REGISTER
contains notices to the public of the proposed
issuance of rules and regulations. The
purpose of these notices is to give interested
persons an opportunity to participate in the
rule making prior to the adoption of the final
rules.
NUCLEAR REGULATORY
COMMISSION
10 CFR Part 51
[Docket No. PRM–51–11]
Sally Shaw; Denial of Petition for
Rulemaking
Nuclear Regulatory
Commission.
ACTION: Denial of petition for
rulemaking.
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AGENCY:
SUMMARY: The Nuclear Regulatory
Commission (NRC) is denying a petition
for rulemaking (PRM) submitted by
Sally Shaw on June 23, 2006. The
petition, docketed as PRM–51–11,
requests that the NRC prepare a
rulemaking to reconcile NUREG–1437,
‘‘Generic Environmental Impact
Statement for License Renewal of
Nuclear Plants’’ (May 1996) (GEIS), for
nuclear power plant operating license
renewal applications with the National
Academy of Sciences’ (NAS), ‘‘Health
Risks From Exposure to Low Levels of
Ionizing Radiation: Biological Effects of
Ionizing Radiation (BEIR) VII, Phase 2,’’
Seventh Ed., 2005 report. The petitioner
believes that this action is necessary
because the BEIR VII report represents
new and significant information on
radiation standards and risk factors that
must be reflected in NRC’s GEIS.
Although the NRC recognizes that the
petition highlighted that BEIR VII
contains a more refined risk assessment
based on additional medical data and a
better dosimetry system, the NRC is
denying PRM–51–11 because it does not
provide significant information or
arguments that were not previously
considered by the Commission.
ADDRESSES: Publicly available
documents related to these petitions and
the NRC’s letter of denial to the
petitioner may be viewed electronically
on public computers in the NRC’s
PublicDocument Room (PDR), 01 F21,
One White Flint North, 11555 Rockville
Pike, Rockville, Maryland. The PDR
reproduction contractor will copy
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documents for a fee. Publicly available
documents created or received at the
NRC after November 1, 1999, are
available electronically at the NRC’s
Electronic Reading Room at https://
www.nrc.gov/reading-rm/adams.html.
From this site, the public can gain entry
into the NRC’s Agencywide Document
Access and Management System
(ADAMS), which provides text and
image files of NRC’s public documents.
If you do not have access to ADAMS or
if there are problems in accessing the
documents located in ADAMS, contact
the PDR reference staff at (800) 387–
4209, (301) 415–4737 or by e-mail to
pdr@nrc.gov.
FOR FURTHER INFORMATION CONTACT:
David T. Diec, telephone (301) 415–
2834, e-mail dtd@nrc.gov, or Andrew
Luu, telephone (301) 415–1078, e-mail
anl@nrc.gov, Office of Nuclear Reactor
Regulation, Nuclear Regulatory
Commission, Washington, DC 20555–
0001.
SUPPLEMENTARY INFORMATION:
The Petition
On November 20, 2006 (71 FR 67072),
the NRC published a notice of receipt of
a petition for rulemaking filed by Sally
Shaw (the petitioner). The petitioner
requested that the NRC reconcile the
GEIS with the NAS BEIR VII report,
which was released in 2005. The GEIS
incorporates data from BEIR V, an
earlier NAS report that was released in
1990. The NRC regulation, Part 10 of the
Code of Federal Regulations Section
51.95(c), requires that the NRC prepare
a supplemental environmental impact
statement (SEIS) to the GEIS. The
findings of the GEIS are set forth in
Table B–1 of Appendix B to subpart A
of 10 CFR part 51 (Table B–1). A copy
of the petition can be found in ADAMS
under accession number ML061770056.
Specifically, the petitioner requests
that the NRC consider the NAS BEIR VII
report as new and significant
information and update the radiological
impacts and conclusions set forth in the
GEIS, including early fatalities, latent
fatalities, and any injury projections
based on this information. The
petitioner asserts that BEIR VII
represents the ‘‘current science,’’ and
states that BEIR VII, unlike BEIR V,
‘‘estimates risks for cancer incidence
rates as well as mortality and also
provides detailed risk figures according
to age of exposure for males and
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females, by cancer type.’’ According to
the petitioner, BEIR VII shows that the
cancer mortality risks for women and
children are much higher than for men.
Further, the petitioner asserts that the
GEIS’s radiological impact analysis is
calculated based on an ‘‘arbitrary and
false’’ threshold dose model, implying
that a dose received below the threshold
would not be of ‘‘regulatory concern.’’
In this regard, the petitioner refers to
BEIR VII, which concludes that there is
no evidence of a ‘‘threshold dose
phenomenon.’’
The petitioner also asserts that the
GEIS reports radiation risks to nuclear
workers of one rem per year based on
BEIR V. The petitioner requests that
these radiation risks be recalculated
using BEIR VII and the latest science in
medical journals, which include
exposure to internal radiation sources
(alpha and beta emitters, via inhalation
or ingestion). Finally, the petitioner
asserts that the radiological impact
analysis contained in the GEIS assumes
that non-stochastic effects will not occur
if the dose equivalent from internal and
external sources combined is less than
50 rem per year and, as such, must be
recalculated in light of BEIR VII.
NRC Evaluation
The petitioner’s request is that the
NRC reconcile the GEIS with the NAS
BEIR VII, 2005 report. The NRC’s
regulations for implementing its
responsibilities under the National
Environmental Policy Act (NEPA) are
contained in 10 CFR part 51,
‘‘Environmental Protection Regulations
for Domestic Licensing and Related
Regulatory Functions.’’ The renewal of
a nuclear power plant operating license
is identified as a major Federal action
significantly affecting the quality of the
human environment, and thus an SEIS
(in conjunction with the GEIS) is
required before the NRC determines
whether to approve or disapprove the
license renewal application. The NRC’s
requirements for renewal of operating
licenses for nuclear power plants are
contained in 10 CFR part 54. The GEIS
assesses environmental impacts that
could be associated with nuclear power
plant license renewal and establishes
generic findings for each type of
environmental impact covering as many
plants as possible. The GEIS reflects the
NRC’s findings regarding those
environmental impacts associated with
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license renewal that are well
understood.
GEIS
The GEIS assesses the various
environmental impacts associated with
license renewal in terms of significance
and assigns one of three significance
levels to a given impact—small,
moderate, or large. A small impact
means that the environmental effects are
not detectable or are so minor that they
will neither destabilize nor noticeably
alter any important attribute of the
resource. For the purpose of assessing
radiological impacts, the NRC has
concluded that those impacts that do
not exceed permissible levels in the
NRC’s regulations are considered small.
A moderate impact means that the
environmental effects are sufficient to
alter noticeably but not to destabilize
important attributes of the resource. A
large impact means that the
environmental effects are clearly
noticeable and are sufficient to
destabilize important attributes of the
resource.
In addition to determining the
significance of environmental impacts
associated with license renewal, the
NRC determines if its analysis can be
applied to all plants and whether
additional mitigation measures would
be warranted. The GEIS sets forth two
categories: Category 1 and Category 2.
Category 1 means that the GEIS analysis
has shown that the environmental
impacts associated with the issue have
been determined to apply either to all
plants or, for some environmental
issues, to plants having a specific type
of cooling system or other specified
plant or site characteristics; a single
significance level (i.e., small, moderate,
or large) has been assigned to the
impacts; mitigation of adverse impacts
associated with the issue has been
considered in the analysis; and it has
been determined that additional plantspecific mitigation measures are not
likely to be sufficiently beneficial to
warrant implementation. Category 2
means that the GEIS analysis does not
meet the criteria of Category 1, and thus,
on that particular environmental issue,
additional plant-specific review is
required. The GEIS findings are set forth
in Table B–1 of Appendix B to subpart
A of 10 CFR part 51.
For each license renewal application,
the NRC will prepare a draft SEIS to
analyze those plant-specific (Category 2)
issues. The SEIS is not required to cover
any Category 1 issues. The draft SEIS is
made available for public comment.
After consideration of any public
comments, the NRC will prepare and
issue a final SEIS under 10 CFR 51.91
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and 51.93. The final SEIS and the GEIS
serve as the requisite NEPA analysis for
any given license renewal application.
The GEIS analysis, as shown in Table
B–1, concluded that both public and
occupational radiation exposures during
any plant refurbishment or plant
operation through the license renewal
term are of a small significance level
and meet all Category 1 criteria. This
conclusion is based on a given
licensee’s adherence to, and if
necessary, NRC enforcement of, the dose
limits as required in 10 CFR part 20,
‘‘Standards for Protection Against
Radiation’’ and in Appendix I to 10 CFR
part 50, ‘‘Numerical Guides for Design
Objectives and Limiting Conditions for
Operation to Meet the Criterion ‘As Low
As Is Reasonably Achievable’ (ALARA)
for Radioactive Material in Light-WaterCooled Nuclear Power Reactor
Effluents.’’ Regulations at 10 CFR part
20 require that a licensee limit the
annual dose to a member of the public
to no more than 0.1 rem (1mSv) total
effective dose equivalent (TEDE). In
addition, 40 CFR part 190,
‘‘Environmental Radiation Protection
Standards For Nuclear Power
Operations,’’ further restricts the
allowable annual dose to a member of
the public to a lower value of 0.025 rem
(0.25 mSv) and to maintain doses to
members of the public that are ALARA.
Finally, 10 CFR 50.34a requires a
nuclear power plant to maintain control
over radioactive gaseous and liquid
effluents produced during normal
operations to dose levels contained in
Appendix I to 10 CFR Part 50, which are
in the range of 0.003 rem (0.03 mSv) to
0.005 rem (0.05 mSv).
BEIR Reports
The risk estimates of human health
effects from radiation were first
evaluated by scientific committees
starting in the 1950s. Since 1972, the
National Academy of Sciences has
published a series of reports on the
biological effects of ionizing radiation
(the BEIR reports), including the BEIR V
report in 1990 and the BEIR VII report
in 2005. The BEIR V and BEIR VII
reports concentrated primarily on
providing a comprehensive review of all
biological and biophysical data
regarding the health effects attributable
to exposures to low doses of ionizing
radiation, ranging between 0 to 10 rem
(0–100 mSv). Although the BEIR VII
committee examined several sources of
epidemiological data (i.e., medical and
occupational exposures), the single most
important source of epidemiological
data is the cohort of 120,000 Japanese
atomic bomb survivors from the cities of
Hiroshima and Nagasaki.
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Three major changes have occurred
after the BEIR V report was published.
First, an additional 12 years of followup medical data are available. Second,
cancer incidence data for the cohort are
available (for BEIR V, only mortality
data were available). The impact of
these two developments has reduced the
uncertainty in the assessment of cancer
risk among the atomic bomb survivors.
Third, the dosimetry system used to
assign radiation exposure to the atomic
bomb survivors was replaced with an
improved dosimetry system. These
changes have improved our
understanding of the health risks
associated with radiation exposure. The
overall risk estimates of the BEIR V and
BEIR VII reports, however, remain
statistically insignificant. In this regard,
the BEIR VII report states: ‘‘in general
the magnitude of estimated risks for
total cancer mortality or leukemia has
not changed greatly from estimates in
past reports such as BEIR V and recent
reports of the United Nations Scientific
Committee on the Effects of Atomic
Radiation (UNSCEAR) and the
International Commission on
Radiological Protection (ICRP). New
data and analyses have reduced
sampling uncertainty, but uncertainties
related to estimating risk for exposure at
low doses and dose rates and
transporting risks from Japanese
A-bomb survivors to the U.S. population
remain large. Uncertainties in
estimating risks of site-specific cancers
are especially large.’’
The NRC staff completed a review of
the BEIR VII report and documented its
findings in the Commission paper
SECY–05–0202, ‘‘Staff Review of the
National Academies Study of the Health
Risks from Exposure to Low Levels of
Ionizing Radiation (BEIR VII),’’ dated
October 29, 2005 (ADAMS accession
number ML052640532). In this paper,
the NRC staff concluded that the
findings presented in the BEIR VII
report agree with the NRC’s current
understanding of the health risks from
exposure to ionizing radiation. The
BEIR VII report’s major conclusion is
that current scientific evidence is
consistent with the hypothesis that
there is a linear, no-threshold dose
response relationship between exposure
to ionizing radiation and the
development of cancer in humans. This
conclusion is consistent with the system
of radiological protection that the NRC
used to develop its regulations and the
GEIS. Therefore, the NRC’s regulations
and the GEIS continue to be adequately
protective of public health and safety
and the environment. Consequently,
none of the findings in the BEIR VII
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report represent new and significant
information when compared to the
findings of the BEIR V report and thus,
there is no need to amend NRC
regulations or the GEIS. The NRC has
determined that a specific rulemaking to
amend 10 CFR Part 51 and by extension,
the GEIS, is not warranted.
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Public Comments
The NRC received a total of 74 public
comments relating to this petition. Of
the 74 comments, 69 supported granting
the petition. No comments opposed the
petition and five comments were not
applicable to this petition. The letters in
support of the petition were essentially
identical and contained one or more of
the following four assertions:
A. Protect the most vulnerable
populations in the regulatory standards.
B. Recognize that ‘‘allowable’’ levels
are not safe.
C. Consider radiation damage from
inhaling or ingesting radionuclides; and
D. Recognize that there is no safe
dose.
A. Protect the Most Vulnerable
Populations in the Regulatory Standards
Although some epidemiological
studies have shown that children,
individuals in poor health, and the
elderly are more radiosensitive to
radiation at high doses and high dose
rates, no adverse health effects have
been observed in these populations at
the doses associated with NRC’s
radiation protection regulations and
standards. The NRC, in NUREG 1850,
‘‘Frequently Asked Questions on
License Renewal of Nuclear Power
Reactors,’’ provides information on a
number of studies that have been
performed to examine the health effects
around nuclear power facilities. These
studies report that there is no
conclusive evidence which shows a
statistical correlation between the low
level radiation dose received by
members of the public living near a
nuclear power plant and their cancer
incidence.
The dose from radioactive gaseous
and liquid effluents is based on the
‘‘maximum exposed individual’’ and
calculated to each of the four age groups
(0–1, 1–11, 11–17, and 17 years and
older). The methodology and guidance
for calculating these doses and the
associated dose conversion factors for
each age group, are contained in
Regulatory Guide 1.109, ‘‘Calculation of
Annual Doses to Man from Routine
Releases of Reactor Effluents for the
Purpose of Evaluating Compliance with
10 CFR Part 50, Appendix I.’’ Nuclear
power reactors implement this
methodology and guidance in
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individual plant radiation protection
programs and operating procedures. The
NRC has concluded that the current
NRC radiation protection standards
continue to ensure adequate protection
of the public. This position is further
reiterated in the Commission Paper
SECY–05–0202. In this paper, the NRC
staff reviewed and evaluated NRC’s
radiation safety regulations and
standards against the findings of the
BEIR VII report. The NRC staff
concluded ‘‘that the findings presented
in the National Academies BEIR VII
report contribute to our understanding
of the heath risks from exposure to
ionizing radiation. The major
conclusion is that current scientific
evidence is consistent with the
hypothesis that there is a linear, nothreshold dose response relationship
between exposure to ionizing radiation
and the development of cancer in
humans.’’ The BEIR VII report’s
conclusion is consistent with the system
of radiological protection that the NRC
used to develop its regulations and the
GEIS. Therefore, the NRC concludes that
the current regulations continue to be
adequately protective of the public
health and safety and the environment.
Consequently, none of the findings in
the BEIR VII report warrant initiating
any immediate change to NRC
regulations or the GEIS.
B. Recognize That ‘‘Allowable’’ Levels
Are Not Safe
Commenter states that these levels are
based on obsolete ‘‘standard man,’’
concept that applies to a healthy, white
male in the prime of his life, and ignore
the more vulnerable fetus, growing
infant, children, and women who,
according to the BEIR VII report, are 37–
50 percent more vulnerable than men to
the harmful effects of ionizing radiation.
Although some epidemiological studies
have shown that children, individuals
in poor health, and the elderly are more
radiosensitive to radiation at high doses
and high dose rates, no adverse health
effects have been observed in these
populations at the doses associated with
NRC’s radiation protection regulations
and standards. The amount of
radioactive material released from
nuclear power facilities is well
measured, closely monitored, and
known to be very small. As shown by
the studies referenced in NUREG–1850,
the radiation dose received by members
of the public from the normal operation
of a nuclear power plant are so low that
no cancers have been observed.
The BEIR VII committee’s preferred
estimate of lifetime attributable risk for
solid cancer incidence and mortality
(Tables 12–13) suggest that females are
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more sensitive than males to radiation
exposure at 10 rem, a level that is 100
times the NRC’s radiation protection
standards specified in 10 CFR Part 20.
The BEIR VII committee’s preferred
estimate of lifetime attributable risk for
leukemia cancer incidence and
mortality (Tables 12–13), moreover,
suggest that males are more sensitive
than females. The BEIR VII committee
uses the 95 percent confidence intervals
associated with estimated lifetime
cancer risk for males and females that
suggest that the apparent gender
difference may not be statistically
significant. Consequently, the BEIR VII
report combined the two risk estimates
and cited an average value which was
also done by the BEIR V committee. A
potential gender difference was not
discussed in the BEIR VII report.
The NRC radiation protection
regulation, 10 CFR 20.1208, requires
each licensee to ensure that the dose
equivalent to the embryo/fetus during
the entire pregnancy, due to the
occupational exposure of a declared
pregnant woman, does not exceed 0.5
rem (5 mSv). These radiation protection
standards continue to ensure adequate
protection of the public health and
safety and the environment.
The petitioner has also requested that
the NRC review an article entitled
‘‘Healthy from the Start: Building a
Better Basis for Environmental Health
Standards—Starting with Radiation,’’
published by the Institute for Energy
and Environmental Research (IEER),
February 2007. This article was not
published in a scientific peer-reviewed
journal and the article’s conclusions do
not appear to have been subjected to an
independent peer review process. The
authors of this article have stated that
there are cause-and-effect relationships
in the statistical associations between
cancer rates and nuclear power reactor
operations. Although it is true that
cancer rates vary among locations, it is
difficult to ascribe the cause of a cluster
of cancers to a specific environmental
agent, such as radiation from a nuclear
power plant. Statistical association
alone does not demonstrate causation.
Also, well-established scientific
methods must be used to demonstrate
that these causal effects are appeared to
be associated over time. Discussions
regarding infants, children, and women
are addressed in section A of this
document.
C. Consider Radiation Damage From
Inhaling or Ingesting Radionuclides
The issue of radiation risks, as
discussed in the GEIS (i.e., Appendix E,
section E 4.1.1), used a reference value
of 1 rem to calculate the estimated
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number of excess cancer fatalities, based
on the BEIR V report. As discussed in
the section titled, ‘‘BEIR Reports,’’ while
the changes between the reports has
increased our understanding of
radiation risk, none of the findings of
the BEIR VII report represent new and
significant information when compared
to the findings of the BEIR V report.
Thus, there is no need to amend NRC
regulations or the GEIS.
Human health effects associated with
ionizing radiation, which the GEIS
classifies as a Category 1 issue, are
divided into two broad categories, nonstochastic and stochastic. The nonstochastic health effects are those in
which the severity varies in direct
relationship with the radiation dose and
for which, according to scientific reports
from ICRP, UNSCEAR, as well as the
BEIR committee, a dose threshold is
known to exist. Radiation-induced
cataract formation is an example of a
non-stochastic effect. The stochastic
health effects are those that occur
randomly and for which the probability
of the effect occurring, rather than its
severity, is assumed to be a linear
function of dose without threshold.
Hereditary effects and cancer incidences
are examples of stochastic effects. For
the mitigation of stochastic health
effects, the NRC endorses the linear, nothreshold dose response model as a
basis for its radiation protection
standards. This model indicates that any
increase in radiation dose, no matter
how small, results in an incremental
increase in the risk of adverse health
effects.
NRC regulations and standards, such
as the annual dose limits contained in
10 CFR Part 20 for members of the
public and for occupational workers,
account for stochastic and nonstochastic health effects of radioactive
material inhaled or ingested into the
human body. For members of the
public, the annual dose limit from
exposure to radiation from an NRC
licensed facility is 0.1 rem. For
occupational workers, there are specific
dose limits to address the stochastic and
non-stochastic health effects. The total
effective dose equivalent limit which
addresses the stochastic health effects is
limited to an annual dose of 5 rem. To
address the non-stochastic health
effects, the annual dose limit to any
individual organ or tissue and the skin,
other than the lens of the eye, is 50 rem;
the annual dose limit to the lens of the
eye is 15 rem. The dose unit is specified
as TEDE in rem. The TEDE dose is the
sum of the deep-dose equivalent (i.e.,
external exposures) and the committed
effective dose equivalent (i.e., internal
exposures received from inhaling or
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ingesting of radioactive material which
includes alpha, beta, gamma, and
neutron emitters). The current dose
regulations and standards contain
adequate radiation safety limits based
on radiation exposures from all types of
radioactive material and therefore,
continue to ensure adequate protection
of the public and occupational workers.
Further, Appendix I to 10 CFR Part 50
provides numerical ALARA dose
criteria for the discharge of radioactive
gaseous and liquid effluents from
nuclear power plants. These dose
objectives are incorporated into each
nuclear power plant’s license
conditions. The NRC collects and
assesses data regarding licensees’
adherence to regulations based on site
visits, audits and inspection records,
and the annual radiological effluent
release reports required to be submitted
to the NRC and concludes that nuclear
power plants continue to maintain their
radioactive effluents to the ALARA dose
criteria.
D. Recognize That There Is No Safe
Dose
The BEIR VII report’s major
conclusion is that current scientific
evidence is consistent with the
hypothesis that there is a linear, nothreshold dose response relationship
between exposure to ionizing radiation
and the development of cancer in
humans. The BEIR VII committee did
not attempt to equate radiation exposure
and safety, nor did it offer any judgment
or opinion on what constitutes a safe
level of radiation exposure. It concludes
that establishing limits on public
exposure to ionizing radiation is the
responsibility of Federal agencies like
the U.S. Environmental Protection
Agency and the NRC. The linear, nothreshold dose response relationship
between exposure to ionizing radiation
and the development of cancer in
humans is consistent with the system of
radiological protection that the NRC
uses as a basis to develop its
regulations. Therefore, the NRC’s
regulations continue to ensure adequate
protection of the public health and
safety and the environment.
Reasons for Denial
The Commission is denying the
petition for rulemaking submitted by
Sally Shaw. The specific issues
contained in the petition are already
adequately addressed in the NRC’s
radiation protection regulations and
standards.
Although this petition is being
denied, the Commission notes that the
current GEIS that referenced the BEIR V,
1999 report, is undergoing planned
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revision and will consider recent
radiological studies, including the BEIR
VII, 2005 report. The summary of
findings as a result of the planned
update will be codified through an
ongoing and routine rulemaking to 10
CFR Part 51, Subpart A, Appendix B,
Table B1—Summary of Findings on
NEPA Issues for License Renewal of
Nuclear Power Plants.
The Commission has concluded that
nuclear plants that are in compliance
with NRC radiation protection
regulations and standards remain
protective of public health and safety
and the environment. The radiological
health and environmental impacts
contained in the GEIS, which are based
on regulatory compliance, remain valid.
For these reasons, the Commission
denies PRM–51–11.
Dated at Rockville, Maryland, this 10th day
of December 2007.
For the Nuclear Regulatory Commission.
Annette L. Vietti-Cook,
Secretary of the Commission.
[FR Doc. E7–24291 Filed 12–13–07; 8:45 am]
BILLING CODE 7590–01–P
DEPARTMENT OF TRANSPORTATION
Federal Aviation Administration
14 CFR Part 39
[Docket No. FAA–2007–0258; Directorate
Identifier 2007–CE–090–AD]
RIN 2120–AA64
Airworthiness Directives; Air Tractor,
Inc. AT–400, AT–500, AT–600, and AT–
800 Series Airplanes
Federal Aviation
Administration (FAA), DOT.
ACTION: Supplemental notice of
proposed rulemaking (NPRM);
Extension of the comment period.
AGENCY:
SUMMARY: We are revising an earlier
proposed airworthiness directive (AD)
that applies to certain Air Tractor, Inc.
(Air Tractor) AT–400, AT–500, AT–600,
and AT–800 series airplanes. The earlier
NPRM proposed to supersede
Airworthiness Directive (AD) 2007–13–
17, which applies to certain Air Tractor
Models AT–602, AT–802, and AT–802A
airplanes. AD 2007–13–17 currently
requires you to repetitively inspect the
engine mount for any cracks, repair or
replace any cracked engine mount, and
report any cracks found to the FAA. The
earlier NPRM proposed to retain the
inspection actions of AD 2007–13–17
for Models AT–602, AT–802, and AT–
802A airplanes, including the
compliance times and effective dates;
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Agencies
[Federal Register Volume 72, Number 240 (Friday, December 14, 2007)]
[Proposed Rules]
[Pages 71083-71086]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E7-24291]
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Proposed Rules
Federal Register
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This section of the FEDERAL REGISTER contains notices to the public of
the proposed issuance of rules and regulations. The purpose of these
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[[Page 71083]]
NUCLEAR REGULATORY COMMISSION
10 CFR Part 51
[Docket No. PRM-51-11]
Sally Shaw; Denial of Petition for Rulemaking
AGENCY: Nuclear Regulatory Commission.
ACTION: Denial of petition for rulemaking.
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SUMMARY: The Nuclear Regulatory Commission (NRC) is denying a petition
for rulemaking (PRM) submitted by Sally Shaw on June 23, 2006. The
petition, docketed as PRM-51-11, requests that the NRC prepare a
rulemaking to reconcile NUREG-1437, ``Generic Environmental Impact
Statement for License Renewal of Nuclear Plants'' (May 1996) (GEIS),
for nuclear power plant operating license renewal applications with the
National Academy of Sciences' (NAS), ``Health Risks From Exposure to
Low Levels of Ionizing Radiation: Biological Effects of Ionizing
Radiation (BEIR) VII, Phase 2,'' Seventh Ed., 2005 report. The
petitioner believes that this action is necessary because the BEIR VII
report represents new and significant information on radiation
standards and risk factors that must be reflected in NRC's GEIS.
Although the NRC recognizes that the petition highlighted that BEIR VII
contains a more refined risk assessment based on additional medical
data and a better dosimetry system, the NRC is denying PRM-51-11
because it does not provide significant information or arguments that
were not previously considered by the Commission.
ADDRESSES: Publicly available documents related to these petitions and
the NRC's letter of denial to the petitioner may be viewed
electronically on public computers in the NRC's PublicDocument Room
(PDR), 01 F21, One White Flint North, 11555 Rockville Pike, Rockville,
Maryland. The PDR reproduction contractor will copy documents for a
fee. Publicly available documents created or received at the NRC after
November 1, 1999, are available electronically at the NRC's Electronic
Reading Room at https://www.nrc.gov/reading-rm/adams.html. From this
site, the public can gain entry into the NRC's Agencywide Document
Access and Management System (ADAMS), which provides text and image
files of NRC's public documents. If you do not have access to ADAMS or
if there are problems in accessing the documents located in ADAMS,
contact the PDR reference staff at (800) 387-4209, (301) 415-4737 or by
e-mail to pdr@nrc.gov.
FOR FURTHER INFORMATION CONTACT: David T. Diec, telephone (301) 415-
2834, e-mail dtd@nrc.gov, or Andrew Luu, telephone (301) 415-1078, e-
mail anl@nrc.gov, Office of Nuclear Reactor Regulation, Nuclear
Regulatory Commission, Washington, DC 20555-0001.
SUPPLEMENTARY INFORMATION:
The Petition
On November 20, 2006 (71 FR 67072), the NRC published a notice of
receipt of a petition for rulemaking filed by Sally Shaw (the
petitioner). The petitioner requested that the NRC reconcile the GEIS
with the NAS BEIR VII report, which was released in 2005. The GEIS
incorporates data from BEIR V, an earlier NAS report that was released
in 1990. The NRC regulation, Part 10 of the Code of Federal Regulations
Section 51.95(c), requires that the NRC prepare a supplemental
environmental impact statement (SEIS) to the GEIS. The findings of the
GEIS are set forth in Table B-1 of Appendix B to subpart A of 10 CFR
part 51 (Table B-1). A copy of the petition can be found in ADAMS under
accession number ML061770056.
Specifically, the petitioner requests that the NRC consider the NAS
BEIR VII report as new and significant information and update the
radiological impacts and conclusions set forth in the GEIS, including
early fatalities, latent fatalities, and any injury projections based
on this information. The petitioner asserts that BEIR VII represents
the ``current science,'' and states that BEIR VII, unlike BEIR V,
``estimates risks for cancer incidence rates as well as mortality and
also provides detailed risk figures according to age of exposure for
males and females, by cancer type.'' According to the petitioner, BEIR
VII shows that the cancer mortality risks for women and children are
much higher than for men. Further, the petitioner asserts that the
GEIS's radiological impact analysis is calculated based on an
``arbitrary and false'' threshold dose model, implying that a dose
received below the threshold would not be of ``regulatory concern.'' In
this regard, the petitioner refers to BEIR VII, which concludes that
there is no evidence of a ``threshold dose phenomenon.''
The petitioner also asserts that the GEIS reports radiation risks
to nuclear workers of one rem per year based on BEIR V. The petitioner
requests that these radiation risks be recalculated using BEIR VII and
the latest science in medical journals, which include exposure to
internal radiation sources (alpha and beta emitters, via inhalation or
ingestion). Finally, the petitioner asserts that the radiological
impact analysis contained in the GEIS assumes that non-stochastic
effects will not occur if the dose equivalent from internal and
external sources combined is less than 50 rem per year and, as such,
must be recalculated in light of BEIR VII.
NRC Evaluation
The petitioner's request is that the NRC reconcile the GEIS with
the NAS BEIR VII, 2005 report. The NRC's regulations for implementing
its responsibilities under the National Environmental Policy Act (NEPA)
are contained in 10 CFR part 51, ``Environmental Protection Regulations
for Domestic Licensing and Related Regulatory Functions.'' The renewal
of a nuclear power plant operating license is identified as a major
Federal action significantly affecting the quality of the human
environment, and thus an SEIS (in conjunction with the GEIS) is
required before the NRC determines whether to approve or disapprove the
license renewal application. The NRC's requirements for renewal of
operating licenses for nuclear power plants are contained in 10 CFR
part 54. The GEIS assesses environmental impacts that could be
associated with nuclear power plant license renewal and establishes
generic findings for each type of environmental impact covering as many
plants as possible. The GEIS reflects the NRC's findings regarding
those environmental impacts associated with
[[Page 71084]]
license renewal that are well understood.
GEIS
The GEIS assesses the various environmental impacts associated with
license renewal in terms of significance and assigns one of three
significance levels to a given impact--small, moderate, or large. A
small impact means that the environmental effects are not detectable or
are so minor that they will neither destabilize nor noticeably alter
any important attribute of the resource. For the purpose of assessing
radiological impacts, the NRC has concluded that those impacts that do
not exceed permissible levels in the NRC's regulations are considered
small. A moderate impact means that the environmental effects are
sufficient to alter noticeably but not to destabilize important
attributes of the resource. A large impact means that the environmental
effects are clearly noticeable and are sufficient to destabilize
important attributes of the resource.
In addition to determining the significance of environmental
impacts associated with license renewal, the NRC determines if its
analysis can be applied to all plants and whether additional mitigation
measures would be warranted. The GEIS sets forth two categories:
Category 1 and Category 2. Category 1 means that the GEIS analysis has
shown that the environmental impacts associated with the issue have
been determined to apply either to all plants or, for some
environmental issues, to plants having a specific type of cooling
system or other specified plant or site characteristics; a single
significance level (i.e., small, moderate, or large) has been assigned
to the impacts; mitigation of adverse impacts associated with the issue
has been considered in the analysis; and it has been determined that
additional plant-specific mitigation measures are not likely to be
sufficiently beneficial to warrant implementation. Category 2 means
that the GEIS analysis does not meet the criteria of Category 1, and
thus, on that particular environmental issue, additional plant-specific
review is required. The GEIS findings are set forth in Table B-1 of
Appendix B to subpart A of 10 CFR part 51.
For each license renewal application, the NRC will prepare a draft
SEIS to analyze those plant-specific (Category 2) issues. The SEIS is
not required to cover any Category 1 issues. The draft SEIS is made
available for public comment. After consideration of any public
comments, the NRC will prepare and issue a final SEIS under 10 CFR
51.91 and 51.93. The final SEIS and the GEIS serve as the requisite
NEPA analysis for any given license renewal application.
The GEIS analysis, as shown in Table B-1, concluded that both
public and occupational radiation exposures during any plant
refurbishment or plant operation through the license renewal term are
of a small significance level and meet all Category 1 criteria. This
conclusion is based on a given licensee's adherence to, and if
necessary, NRC enforcement of, the dose limits as required in 10 CFR
part 20, ``Standards for Protection Against Radiation'' and in Appendix
I to 10 CFR part 50, ``Numerical Guides for Design Objectives and
Limiting Conditions for Operation to Meet the Criterion `As Low As Is
Reasonably Achievable' (ALARA) for Radioactive Material in Light-Water-
Cooled Nuclear Power Reactor Effluents.'' Regulations at 10 CFR part 20
require that a licensee limit the annual dose to a member of the public
to no more than 0.1 rem (1mSv) total effective dose equivalent (TEDE).
In addition, 40 CFR part 190, ``Environmental Radiation Protection
Standards For Nuclear Power Operations,'' further restricts the
allowable annual dose to a member of the public to a lower value of
0.025 rem (0.25 mSv) and to maintain doses to members of the public
that are ALARA. Finally, 10 CFR 50.34a requires a nuclear power plant
to maintain control over radioactive gaseous and liquid effluents
produced during normal operations to dose levels contained in Appendix
I to 10 CFR Part 50, which are in the range of 0.003 rem (0.03 mSv) to
0.005 rem (0.05 mSv).
BEIR Reports
The risk estimates of human health effects from radiation were
first evaluated by scientific committees starting in the 1950s. Since
1972, the National Academy of Sciences has published a series of
reports on the biological effects of ionizing radiation (the BEIR
reports), including the BEIR V report in 1990 and the BEIR VII report
in 2005. The BEIR V and BEIR VII reports concentrated primarily on
providing a comprehensive review of all biological and biophysical data
regarding the health effects attributable to exposures to low doses of
ionizing radiation, ranging between 0 to 10 rem (0-100 mSv). Although
the BEIR VII committee examined several sources of epidemiological data
(i.e., medical and occupational exposures), the single most important
source of epidemiological data is the cohort of 120,000 Japanese atomic
bomb survivors from the cities of Hiroshima and Nagasaki.
Three major changes have occurred after the BEIR V report was
published. First, an additional 12 years of follow-up medical data are
available. Second, cancer incidence data for the cohort are available
(for BEIR V, only mortality data were available). The impact of these
two developments has reduced the uncertainty in the assessment of
cancer risk among the atomic bomb survivors. Third, the dosimetry
system used to assign radiation exposure to the atomic bomb survivors
was replaced with an improved dosimetry system. These changes have
improved our understanding of the health risks associated with
radiation exposure. The overall risk estimates of the BEIR V and BEIR
VII reports, however, remain statistically insignificant. In this
regard, the BEIR VII report states: ``in general the magnitude of
estimated risks for total cancer mortality or leukemia has not changed
greatly from estimates in past reports such as BEIR V and recent
reports of the United Nations Scientific Committee on the Effects of
Atomic Radiation (UNSCEAR) and the International Commission on
Radiological Protection (ICRP). New data and analyses have reduced
sampling uncertainty, but uncertainties related to estimating risk for
exposure at low doses and dose rates and transporting risks from
Japanese A-bomb survivors to the U.S. population remain large.
Uncertainties in estimating risks of site-specific cancers are
especially large.''
The NRC staff completed a review of the BEIR VII report and
documented its findings in the Commission paper SECY-05-0202, ``Staff
Review of the National Academies Study of the Health Risks from
Exposure to Low Levels of Ionizing Radiation (BEIR VII),'' dated
October 29, 2005 (ADAMS accession number ML052640532). In this paper,
the NRC staff concluded that the findings presented in the BEIR VII
report agree with the NRC's current understanding of the health risks
from exposure to ionizing radiation. The BEIR VII report's major
conclusion is that current scientific evidence is consistent with the
hypothesis that there is a linear, no-threshold dose response
relationship between exposure to ionizing radiation and the development
of cancer in humans. This conclusion is consistent with the system of
radiological protection that the NRC used to develop its regulations
and the GEIS. Therefore, the NRC's regulations and the GEIS continue to
be adequately protective of public health and safety and the
environment. Consequently, none of the findings in the BEIR VII
[[Page 71085]]
report represent new and significant information when compared to the
findings of the BEIR V report and thus, there is no need to amend NRC
regulations or the GEIS. The NRC has determined that a specific
rulemaking to amend 10 CFR Part 51 and by extension, the GEIS, is not
warranted.
Public Comments
The NRC received a total of 74 public comments relating to this
petition. Of the 74 comments, 69 supported granting the petition. No
comments opposed the petition and five comments were not applicable to
this petition. The letters in support of the petition were essentially
identical and contained one or more of the following four assertions:
A. Protect the most vulnerable populations in the regulatory
standards.
B. Recognize that ``allowable'' levels are not safe.
C. Consider radiation damage from inhaling or ingesting
radionuclides; and
D. Recognize that there is no safe dose.
A. Protect the Most Vulnerable Populations in the Regulatory Standards
Although some epidemiological studies have shown that children,
individuals in poor health, and the elderly are more radiosensitive to
radiation at high doses and high dose rates, no adverse health effects
have been observed in these populations at the doses associated with
NRC's radiation protection regulations and standards. The NRC, in NUREG
1850, ``Frequently Asked Questions on License Renewal of Nuclear Power
Reactors,'' provides information on a number of studies that have been
performed to examine the health effects around nuclear power
facilities. These studies report that there is no conclusive evidence
which shows a statistical correlation between the low level radiation
dose received by members of the public living near a nuclear power
plant and their cancer incidence.
The dose from radioactive gaseous and liquid effluents is based on
the ``maximum exposed individual'' and calculated to each of the four
age groups (0-1, 1-11, 11-17, and 17 years and older). The methodology
and guidance for calculating these doses and the associated dose
conversion factors for each age group, are contained in Regulatory
Guide 1.109, ``Calculation of Annual Doses to Man from Routine Releases
of Reactor Effluents for the Purpose of Evaluating Compliance with 10
CFR Part 50, Appendix I.'' Nuclear power reactors implement this
methodology and guidance in individual plant radiation protection
programs and operating procedures. The NRC has concluded that the
current NRC radiation protection standards continue to ensure adequate
protection of the public. This position is further reiterated in the
Commission Paper SECY-05-0202. In this paper, the NRC staff reviewed
and evaluated NRC's radiation safety regulations and standards against
the findings of the BEIR VII report. The NRC staff concluded ``that the
findings presented in the National Academies BEIR VII report contribute
to our understanding of the heath risks from exposure to ionizing
radiation. The major conclusion is that current scientific evidence is
consistent with the hypothesis that there is a linear, no-threshold
dose response relationship between exposure to ionizing radiation and
the development of cancer in humans.'' The BEIR VII report's conclusion
is consistent with the system of radiological protection that the NRC
used to develop its regulations and the GEIS. Therefore, the NRC
concludes that the current regulations continue to be adequately
protective of the public health and safety and the environment.
Consequently, none of the findings in the BEIR VII report warrant
initiating any immediate change to NRC regulations or the GEIS.
B. Recognize That ``Allowable'' Levels Are Not Safe
Commenter states that these levels are based on obsolete ``standard
man,'' concept that applies to a healthy, white male in the prime of
his life, and ignore the more vulnerable fetus, growing infant,
children, and women who, according to the BEIR VII report, are 37-50
percent more vulnerable than men to the harmful effects of ionizing
radiation. Although some epidemiological studies have shown that
children, individuals in poor health, and the elderly are more
radiosensitive to radiation at high doses and high dose rates, no
adverse health effects have been observed in these populations at the
doses associated with NRC's radiation protection regulations and
standards. The amount of radioactive material released from nuclear
power facilities is well measured, closely monitored, and known to be
very small. As shown by the studies referenced in NUREG-1850, the
radiation dose received by members of the public from the normal
operation of a nuclear power plant are so low that no cancers have been
observed.
The BEIR VII committee's preferred estimate of lifetime
attributable risk for solid cancer incidence and mortality (Tables 12-
13) suggest that females are more sensitive than males to radiation
exposure at 10 rem, a level that is 100 times the NRC's radiation
protection standards specified in 10 CFR Part 20. The BEIR VII
committee's preferred estimate of lifetime attributable risk for
leukemia cancer incidence and mortality (Tables 12-13), moreover,
suggest that males are more sensitive than females. The BEIR VII
committee uses the 95 percent confidence intervals associated with
estimated lifetime cancer risk for males and females that suggest that
the apparent gender difference may not be statistically significant.
Consequently, the BEIR VII report combined the two risk estimates and
cited an average value which was also done by the BEIR V committee. A
potential gender difference was not discussed in the BEIR VII report.
The NRC radiation protection regulation, 10 CFR 20.1208, requires
each licensee to ensure that the dose equivalent to the embryo/fetus
during the entire pregnancy, due to the occupational exposure of a
declared pregnant woman, does not exceed 0.5 rem (5 mSv). These
radiation protection standards continue to ensure adequate protection
of the public health and safety and the environment.
The petitioner has also requested that the NRC review an article
entitled ``Healthy from the Start: Building a Better Basis for
Environmental Health Standards--Starting with Radiation,'' published by
the Institute for Energy and Environmental Research (IEER), February
2007. This article was not published in a scientific peer-reviewed
journal and the article's conclusions do not appear to have been
subjected to an independent peer review process. The authors of this
article have stated that there are cause-and-effect relationships in
the statistical associations between cancer rates and nuclear power
reactor operations. Although it is true that cancer rates vary among
locations, it is difficult to ascribe the cause of a cluster of cancers
to a specific environmental agent, such as radiation from a nuclear
power plant. Statistical association alone does not demonstrate
causation. Also, well-established scientific methods must be used to
demonstrate that these causal effects are appeared to be associated
over time. Discussions regarding infants, children, and women are
addressed in section A of this document.
C. Consider Radiation Damage From Inhaling or Ingesting Radionuclides
The issue of radiation risks, as discussed in the GEIS (i.e.,
Appendix E, section E 4.1.1), used a reference value of 1 rem to
calculate the estimated
[[Page 71086]]
number of excess cancer fatalities, based on the BEIR V report. As
discussed in the section titled, ``BEIR Reports,'' while the changes
between the reports has increased our understanding of radiation risk,
none of the findings of the BEIR VII report represent new and
significant information when compared to the findings of the BEIR V
report. Thus, there is no need to amend NRC regulations or the GEIS.
Human health effects associated with ionizing radiation, which the
GEIS classifies as a Category 1 issue, are divided into two broad
categories, non-stochastic and stochastic. The non-stochastic health
effects are those in which the severity varies in direct relationship
with the radiation dose and for which, according to scientific reports
from ICRP, UNSCEAR, as well as the BEIR committee, a dose threshold is
known to exist. Radiation-induced cataract formation is an example of a
non-stochastic effect. The stochastic health effects are those that
occur randomly and for which the probability of the effect occurring,
rather than its severity, is assumed to be a linear function of dose
without threshold. Hereditary effects and cancer incidences are
examples of stochastic effects. For the mitigation of stochastic health
effects, the NRC endorses the linear, no-threshold dose response model
as a basis for its radiation protection standards. This model indicates
that any increase in radiation dose, no matter how small, results in an
incremental increase in the risk of adverse health effects.
NRC regulations and standards, such as the annual dose limits
contained in 10 CFR Part 20 for members of the public and for
occupational workers, account for stochastic and non-stochastic health
effects of radioactive material inhaled or ingested into the human
body. For members of the public, the annual dose limit from exposure to
radiation from an NRC licensed facility is 0.1 rem. For occupational
workers, there are specific dose limits to address the stochastic and
non-stochastic health effects. The total effective dose equivalent
limit which addresses the stochastic health effects is limited to an
annual dose of 5 rem. To address the non-stochastic health effects, the
annual dose limit to any individual organ or tissue and the skin, other
than the lens of the eye, is 50 rem; the annual dose limit to the lens
of the eye is 15 rem. The dose unit is specified as TEDE in rem. The
TEDE dose is the sum of the deep-dose equivalent (i.e., external
exposures) and the committed effective dose equivalent (i.e., internal
exposures received from inhaling or ingesting of radioactive material
which includes alpha, beta, gamma, and neutron emitters). The current
dose regulations and standards contain adequate radiation safety limits
based on radiation exposures from all types of radioactive material and
therefore, continue to ensure adequate protection of the public and
occupational workers.
Further, Appendix I to 10 CFR Part 50 provides numerical ALARA dose
criteria for the discharge of radioactive gaseous and liquid effluents
from nuclear power plants. These dose objectives are incorporated into
each nuclear power plant's license conditions. The NRC collects and
assesses data regarding licensees' adherence to regulations based on
site visits, audits and inspection records, and the annual radiological
effluent release reports required to be submitted to the NRC and
concludes that nuclear power plants continue to maintain their
radioactive effluents to the ALARA dose criteria.
D. Recognize That There Is No Safe Dose
The BEIR VII report's major conclusion is that current scientific
evidence is consistent with the hypothesis that there is a linear, no-
threshold dose response relationship between exposure to ionizing
radiation and the development of cancer in humans. The BEIR VII
committee did not attempt to equate radiation exposure and safety, nor
did it offer any judgment or opinion on what constitutes a safe level
of radiation exposure. It concludes that establishing limits on public
exposure to ionizing radiation is the responsibility of Federal
agencies like the U.S. Environmental Protection Agency and the NRC. The
linear, no-threshold dose response relationship between exposure to
ionizing radiation and the development of cancer in humans is
consistent with the system of radiological protection that the NRC uses
as a basis to develop its regulations. Therefore, the NRC's regulations
continue to ensure adequate protection of the public health and safety
and the environment.
Reasons for Denial
The Commission is denying the petition for rulemaking submitted by
Sally Shaw. The specific issues contained in the petition are already
adequately addressed in the NRC's radiation protection regulations and
standards.
Although this petition is being denied, the Commission notes that
the current GEIS that referenced the BEIR V, 1999 report, is undergoing
planned revision and will consider recent radiological studies,
including the BEIR VII, 2005 report. The summary of findings as a
result of the planned update will be codified through an ongoing and
routine rulemaking to 10 CFR Part 51, Subpart A, Appendix B, Table B1--
Summary of Findings on NEPA Issues for License Renewal of Nuclear Power
Plants.
The Commission has concluded that nuclear plants that are in
compliance with NRC radiation protection regulations and standards
remain protective of public health and safety and the environment. The
radiological health and environmental impacts contained in the GEIS,
which are based on regulatory compliance, remain valid.
For these reasons, the Commission denies PRM-51-11.
Dated at Rockville, Maryland, this 10th day of December 2007.
For the Nuclear Regulatory Commission.
Annette L. Vietti-Cook,
Secretary of the Commission.
[FR Doc. E7-24291 Filed 12-13-07; 8:45 am]
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