Endangered and Threatened Wildlife; 90-Day Finding on Petitions To List the Northeastern Pacific Ocean Distinct Population Segment of Great White Shark as Threatened or Endangered Under the Endangered Species Act, 59582-59589 [2012-23963]
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DEPARTMENT OF COMMERCE
National Ocean and Atmospheric
Administration
50 CFR Parts 223 and 224
[Docket No. 120807313–2313–01]
RIN 0648–XC154
Endangered and Threatened Wildlife;
90-Day Finding on Petitions To List the
Northeastern Pacific Ocean Distinct
Population Segment of Great White
Shark as Threatened or Endangered
Under the Endangered Species Act
National Marine Fisheries
Service (NMFS), National Oceanic and
Atmospheric Administration (NOAA),
Commerce.
ACTION: 90-day petition finding, request
for information, and initiation of status
review.
AGENCY:
We, NMFS, announce a 90day finding on two petitions received to
list the northeastern Pacific Ocean
population of great white shark
(Carcharodon carcharias) as a
threatened or endangered distinct
population segment (DPS) under the
Endangered Species Act (ESA) and to
designate critical habitat concurrently
with the listing. We find that the
petitions and information in our files
present substantial scientific or
commercial information indicating that
the petitioned action may be warranted.
We will conduct a status review of the
species to determine if the petitioned
action is warranted. To ensure that the
status review is comprehensive, we are
soliciting scientific and commercial
information pertaining to this species
from any interested party.
DATES: Information and comments on
the subject action must be received by
November 27, 2012.
ADDRESSES: You may submit comments,
information, or data, identified by
‘‘NOAA–NMFS–2012–0176’’ by any one
of the following methods:
• Electronic Submissions: Submit all
electronic comments via the Federal
eRulemaking Portal https://
www.regulations.gov. To submit
comments via the e-Rulemaking Portal,
first click the ‘‘submit a comment’’ icon,
then enter ‘‘NOAA–NMFS–2012–0176’’
in the keyword search. Locate the
document you wish to comment on
from the resulting list and click on the
‘‘Submit a Comment’’ icon on the right
of that line.
• Mail or hand-delivery: Protected
Resources Division, Southwest Region,
NMFS, 501 West Ocean Blvd., Suite
4200, Long Beach, CA 90802–4213.
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Instructions: All comments received
are a part of the public record and may
be posted to https://www.regulations.gov
without change. All personally
identifiable information (for example,
name, address, etc.) voluntarily
submitted by the commenter may be
publicly accessible. Do not submit
confidential business information or
other information you wish to protect
from public disclosure. NMFS will
accept anonymous comments.
Attachments to electronic comments
will be accepted in Microsoft Word,
Excel, Corel WordPerfect, or Adobe PDF
file formats only.
FOR FURTHER INFORMATION CONTACT:
Craig Wingert, NMFS, Southwest
Region, (562) 980–4021; or Marta
Nammack, NMFS, Office of Protected
Resources, (301) 427–8469.
SUPPLEMENTARY INFORMATION:
Background
On June 25, 2012, we received a
petition from WildEarth Guardians to
list the northeastern Pacific Ocean DPS
of great white shark (Carcharodon
carcharias) as threatened or endangered
under the ESA. The petitioners also
requested that critical habitat be
designated for this DPS under the ESA.
On August 13, 2012, we received a
second petition, filed jointly by Oceana,
Center for Biological Diversity (CBD),
and Shark Stewards, to list the
northeastern Pacific Ocean DPS of white
shark (another common name for the
great white shark) under the ESA and
designate critical habitat. Both petitions
bring forth much of the same or related
factual information on the biology and
ecology of great white sharks, and raise
several identical or similar issues
related to potential factors affecting this
species. As a result, we are considering
both petitions simultaneously in this 90day finding. Copies of the petitions are
available upon request (see ADDRESSES,
above).
ESA Statutory, Regulatory, and Policy
Provisions and Evaluation Framework
Section 4(b)(3)(A) of the ESA of 1973,
as amended (16 U.S.C. 1531 et seq.),
requires, to the maximum extent
practicable, that within 90 days of
receipt of a petition to list a species as
threatened or endangered, the Secretary
of Commerce make a finding on whether
that petition presents substantial
scientific or commercial information
indicating that the petitioned action
may be warranted, and to promptly
publish such finding in the Federal
Register (16 U.S.C. 1533(b)(3)(A)). When
it is found that substantial scientific or
commercial information in a petition
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indicates the petitioned action may be
warranted (a ‘‘positive 90-day finding’’),
we are required to promptly commence
a review of the status of the species
concerned during which we will
conduct a comprehensive review of the
best available scientific and commercial
information. In such cases, we conclude
the status review with a finding
published in the Federal Register as to
whether or not the petitioned action is
warranted within 12 months of receipt
of the petition. Because the finding at
the 12-month stage is based on a
thorough review of the available
information, as compared to the more
limited scope of review at the 90-day
stage, a ‘‘may be warranted’’ finding
does not prejudge the outcome of the
status review.
Under the ESA, a listing
determination may address a species,
which is defined to also include any
subspecies and, for vertebrate species,
any DPS which interbreeds when
mature (16 U.S.C. 1532(16)). A joint
NMFS-U.S. Fish and Wildlife Service
(USFWS) (jointly, ‘‘the Services’’) policy
clarifies the agencies’ interpretation of
the phrase ‘‘distinct population
segment’’ for the purposes of listing,
delisting, and reclassifying a species
under the ESA (61 FR 4722; February 7,
1996). A species, subspecies, or DPS is
‘‘endangered’’ if it is in danger of
extinction throughout all or a significant
portion of its range, and ‘‘threatened’’ if
it is likely to become endangered within
the foreseeable future throughout all or
a significant portion of its range (16
U.S.C. 1532(6) and (20)). Pursuant to the
ESA and our implementing regulations,
we determine whether species are
threatened or endangered based on any
one or a combination of the following
factors: (1) The present or threatened
destruction, modification, or
curtailment of its habitat or range; (2)
overutilization for commercial,
recreational, scientific, or educational
purposes; (3) disease or predation; (4)
the inadequacy of existing regulatory
mechanisms; and (5) any other natural
or manmade factors affecting the
species’ continued existence (16 U.S.C.
1533(a)(1), 50 CFR 424.11(c)).
ESA implementing regulations define
‘‘substantial information’’ in the context
of reviewing a petition to list, delist, or
reclassify a species as the amount of
information that would lead a
reasonable person to believe that the
measure proposed in the petition may
be warranted (50 CFR 424.14(b)). In
evaluating whether substantial
information is contained in a petition,
the Secretary must consider whether the
petition: (1) Clearly indicates the
administrative measure recommended
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and gives the scientific and any
common name of the species involved;
(2) contains detailed narrative
justification for the recommended
measure, describing, based on available
information, past and present numbers
and distribution of the species involved
and any threats faced by the species; (3)
provides information regarding the
status of the species over all or a
significant portion of its range; and (4)
is accompanied by the appropriate
supporting documentation in the form
of bibliographic references, reprints of
pertinent publications, copies of reports
or letters from authorities, and maps (50
CFR 424.14(b)(2)).
Judicial decisions have clarified the
appropriate scope and limitations of the
Services’ review of petitions at the 90day finding stage, in making a
determination that a petitioned action
‘‘may be’’ warranted. As a general
matter, these decisions hold that a
petition need not establish a ‘‘strong
likelihood’’ or a ‘‘high probability’’ that
a species is either threatened or
endangered to support a positive 90-day
finding.
We evaluate the petitioners’ request
based upon the information in the
petition including its references and the
information readily available in our
files. We do not conduct additional
research and we do not solicit
information from parties outside the
agency to help us in evaluating the
petition. We will accept the petitioners’
sources and characterizations of the
information presented if they appear to
be based on accepted scientific
principles, unless we have specific
information in our files indicating the
petition’s information is incorrect,
unreliable, obsolete, or otherwise
irrelevant to the requested action.
Information that is susceptible to more
than one interpretation or that is
contradicted by other available
information will not be dismissed at the
90-day finding stage, so long as it is
reliable and a reasonable person would
conclude it supports the petitioners’
assertions. In other words, conclusive
information indicating the species may
meet the ESA’s requirements for listing
is not required to make a positive 90day finding. We will not conclude that
a lack of specific information negates a
positive 90-day finding if a reasonable
person would conclude that the
uncertainty from the lack of information
suggests an extinction risk of concern
for the species at issue.
To make a 90-day finding on a
petition to list a species, we evaluate
whether the petition presents
substantial scientific or commercial
information indicating the subject
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species may be either threatened or
endangered, as defined by the ESA.
First, we evaluate whether the
information presented in the petition,
along with the information readily
available in our files, indicates that the
petitioned entity constitutes a ‘‘species’’
eligible for listing under the ESA. Next,
we evaluate whether the information
indicates that the species faces an
extinction risk that is cause for concern;
this may be indicated in information
expressly discussing the species’ status
and trends, or in information describing
impacts and threats to the species. We
evaluate any information on specific
demographic factors pertinent to
evaluating extinction risk for the species
(e.g., population abundance and trends,
productivity, spatial structure, age
structure, sex ratio, diversity, current
and historical range, habitat integrity or
fragmentation), and the potential
contribution of identified demographic
risks to extinction risk for the species.
We then evaluate the potential links
between these demographic risks and
the causative impacts and threats
identified in section 4(a)(1).
Information presented on impacts or
threats should be specific to the species
and should reasonably suggest that one
or more of these factors may be
operative threats that act or have acted
on the species to the point that it may
warrant protection under the ESA.
Broad statements about generalized
threats to the species, or identification
of factors that could negatively impact
a species, do not constitute substantial
information indicating that listing may
be warranted. We look for information
indicating that not only is the particular
species exposed to a factor, but that the
species may be responding in a negative
fashion; then we assess the potential
significance of that negative response.
Many petitions identify risk
classifications made by nongovernmental organizations, such as the
International Union on the Conservation
of Nature (IUCN), the American
Fisheries Society, or NatureServe, as
evidence of extinction risk for a species.
Risk classifications by other
organizations or made under other
Federal or state statutes may be
informative, but the classification alone
does not provide the rationale for a
positive 90-day finding under the ESA.
For example, as explained by
NatureServe, their assessments of a
species’ conservation status do ‘‘not
constitute a recommendation by
NatureServe for listing under the U.S.
Endangered Species Act’’ because
NatureServe assessments ‘‘have
different criteria, evidence
requirements, purposes and taxonomic
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coverage than government lists of
endangered and threatened species, and
therefore these two types of lists should
not be expected to coincide’’ (https://
www.natureserve.org/prodServices/
statusAssessment.jsp). Thus, when a
petition cites such classifications, we
will evaluate the source of information
that the classification is based upon in
light of the standards on extinction risk
and impacts or threats discussed above.
Distribution and Life History of the
Great White Shark
The great white shark (also known as
‘‘white shark’’) is a circumglobal species
that resides primarily in temperate and
sub-tropical waters (Compagno et al.,
1997; Domeier and Nasby-Lucas, 2006;
Domeier et al., 2012). White sharks
commonly inhabit coastal and
continental shelf waters, although they
have been observed entering marine
bays, estuaries, lagoons, and harbors
(Compagno et al., 1997). Recent studies
suggest that these sharks also spend
considerable amount of time in open
ocean habitats thousands of kilometers
from shore (Domeier, 2012). Areas likely
to attract adult white sharks include
coastal waters adjacent to pinniped
colonies or haulout sites, as these are
favored prey species (Klimley et al.,
1996; Hussey et al., 2012). Known prey
of white sharks also includes a wide
range of other species from smaller
demersal fish, such as rockfish, to giant
pelagic species, such as tuna and
swordfish, as well as sea turtles,
seabirds, cetaceans, and other species of
sharks (Fergusson, 1996; Long and
Jones, 1996; Wilson and Patyten, 2008;
IUCN, 2009; Santana-Morales et al.,
2012). White sharks are recognized as
apex predators throughout the oceanic
and coastal marine environments where
they occur, and may play an important
role in ecosystem balance and
population control for a number of other
marine species (Myers et al., 2007;
Wilson and Patyten, 2008). White sharks
demonstrate the ability to undertake
transoceanic migrations to specific
locations in patterns that appear to be
predictable (Boustany et al., 2002;
Jorgensen et al., 2010; Chapple et al.,
2011; Domeier, 2012).
Great white sharks are distinguished
by their stout spindle-shaped body,
moderately long and bluntly conical
snout, five long gill slits, large falcate
first dorsal fin with free rear tip located
over the pectoral inner margins,
pivoting second dorsal and anal fins,
white ventral body color, and lack of
any secondary keels on the base of the
caudal fin. The teeth are large, flat, and
triangular shaped, with blade-like
serrations, although teeth in the rear of
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the mouth get progressively smaller and
sometimes lack serration, especially in
younger sharks (Compagno et al., 1997;
FAO, 2012). The maximum size of this
species has not been established, but
has been estimated at about 6 m (19 ft),
and possibly up to 6.4 m (21 ft), or more
(Cailliet et al., 1985; Wilson and
Patyten, 2008; IUCN, 2009). Estimated
weight of the largest individuals is
nearly 3,000 kg (6,600 lbs) (Cailliet et
al., 1985; Anderson et al., 2011).
Available information on the general
life history pattern of white sharks
suggests that females mature at about
12–14 years of age, and about 4–5 m
(13–16 ft) in length. Males mature at 9–
10 years old, and about 3.5–4.1 m (11.5–
13.5 ft) in length (Compagno et al.,
1997). It is believed that females give
birth at 2 or 3-year intervals to litters of
2–10 pups that are 1–1.5 m (3.3–4.9 ft)
in length after a 12–22 month gestation
(Francis, 1996; Wilson and Patyten,
2008; Domeier, 2012). Embryos are
oophagus, meaning they consume and
store yolk in their stomachs (Francis,
1996; Uchida et al., 1996), and
viviparous (live) birth of pups likely
occurs sometime between May and
October (Domeier, 2012). Specific
knowledge of pup survival rates is not
available, but is estimated to be low
(CITES, 2004).
Primary concentrations of white
sharks occur in South Africa, Australia
and New Zealand, and the northeastern
Pacific Ocean, with other white sharks
observed in the north Atlantic and the
Mediterranean (Boustany et al., 2002;
Domeier and Nasby-Lucas, 2006; Weng
et al., 2007; Jorgensen et al., 2010).
Genetic and migration studies provide
evidence that these may represent
separate populations (Jorgensen et al.,
2010). Mitochondrial DNA suggests at
least three matrilineal populations:
South Africa/northwest Atlantic;
southwest Pacific; and northeastern
Pacific (Gubili et al., 2012). Although
the southwestern Pacific and
northeastern Pacific populations could
potentially interbreed, the genetic
sampling indicates that these two
populations are largely reproductively
isolated. It has been suggested that the
northeastern Pacific population was
founded by relatively few sharks within
the last 200,000 years, and hasn’t mixed
with other shark populations near
Australia or South Africa since (Hance,
2009; Jorgensen et al., 2010).
White sharks in the northeastern
Pacific Ocean have been observed from
Baja California to the Bering Sea (Kato,
1965; COSEWIC, 2006) and offshore out
to Hawaii. Using satellite and acoustic
telemetry, researchers have followed
movements of white sharks in the
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northeastern Pacific Ocean and
discovered patterns of site fidelity and
repeated homing in structured seasonal
migrations, including fixed destinations,
schedules, and routes (Boustany et al.,
2002; Jorgensen et al., 2010). As a result,
three core areas have been identified in
the central and northeastern Pacific: (1)
North American shelf waters; (2) slope
and offshore waters of Hawaii; and (3)
an area between the North American
coast and Hawaii termed the ‘‘white
´
shark cafe’’ or Shared Offshore Foraging
Area (SOFA) (Jorgensen et al., 2010;
Anderson et al., 2011; Domeier, 2012).
Each winter, great white sharks leave
coastal aggregation sites off of central
˜
California (Farallon Islands/Ano Nuevo/
Point Reyes) and migrate 2000–5000 km
offshore to subtropical and tropical
pelagic habitats, returning to coastal
aggregation sites in late summer. Site
fidelity in North American coastal
hotspots has also been documented
using photo-identification (Jorgensen et
al., 2010; Chapple et al., 2011; SosaNishizaki et al., 2012). Guadalupe
Island, located 250 miles off the coast of
Baja California, Mexico, is also a
preferred aggregation site for adults
(Sosa-Nishizaki et al., 2012). Adult
males annually migrate from preferred
aggregation sites to the SOFA/white
´
shark cafe. Females have been observed
to migrate biennially between preferred
aggregation sites and the area
´
surrounding the SOFA/white shark cafe,
usually after males have returned to
coastal aggregation sites (Domeier,
2012).
The coastal areas of southern
California and Baja California, Mexico,
appear to be important nursery areas
hosting large concentrations of youngof-the-year (YOY) and juvenile great
white sharks (Dewar et al. 2004; Weng
´
˜
et al., 2007; Galvan-Magana et al., 2011;
Domeier, 2012; Santana-Morales et al.,
2012). Information gained from the
records of white shark bycatch in
California and Baja fisheries, including
gillnet, seine-net, and hook and line
fisheries (Lowe et al., 2012; SantanaMorales et al., 2012), along with
relatively consistent reporting of
juvenile white shark observations along
the southern California coast, lend
support to the assertion that this area is
important developmental habitat for
white sharks before they mature into
larger adults. Estimates of abundance
have not been available historically, but
recent studies have suggested the
population size at two known
aggregation sites (Farallon Islands/
Central California and Guadalupe
Island) in the northeastern Pacific
Ocean is around 340 sub-adults and
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adults (Chapple et al., 2011; SosaNishizaki et al., 2012).
Analysis of the Petitions and
Information Readily Available in
NMFS Files
The two petitions request the same
action, to list the northeastern Pacific
Ocean (NEP) DPS of great white shark
(or white shark) as endangered or
threatened under the ESA and to
designate critical habitat for the DPS.
Therefore, we evaluated the information
provided in both petitions and readily
available in our files to determine if the
petitions presented substantial scientific
or commercial information indicating
that the petitioned action may be
warranted. Both petitions contain
information on the species, including
the taxonomy, species description,
geographic distribution, habitat,
population status and trends, and
factors contributing to the species’
decline. Both petitions state that a
primary threat to the NEP population of
white shark is exploitation by fishing
(historical and current) and bycatch in
fisheries. Both petitions also assert that
the lack of adequate regulatory
protection worldwide, bioaccumulation
of contaminants, and habitat
degradation, as well as the species’
biological constraints, increase the
susceptibility of the NEP population of
white shark to extinction.
According to both petitions, the NEP
population of white shark qualifies as a
DPS because the NEP population is both
discrete and significant, as defined
under the Services’ DPS policy (61 FR
4722; February 7, 1996). The WildEarth
Guardians petition asserts that all of the
five causal factors in section 4(a)(1) of
the ESA are adversely affecting the
continued existence of the NEP
population, whereas the Oceana et al.
petition does not discuss disease and
predation as a factor that is adversely
affecting the NEP population. In the
following sections, we analyze the
information presented by the petitions
and in our files on the qualification of
the NEP population of white shark as a
DPS and the specific ESA section 4(a)(1)
factors affecting the population’s risk of
extinction.
Qualification of Northeastern Pacific
Ocean Population as a DPS
Both petitions assert that the NEP
population of white shark qualifies as a
DPS, because it is both a discrete and
significant population segment of the
species, as defined in the NMFS and
USFWS policy on DPSs (61 FR 4722;
February 7, 1996). First, the petitions
state that the NEP population is discrete
based on both genetic and spatial
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separation from other populations of
white shark. Genetic analyses indicate
that the NEP population of white sharks
is similar to and descended from the
Australian/New Zealand (ANZ)
population (Jorgensen et al., 2010;
Gubili et al., 2012). The NEP population
was likely established during the Late
Pleistocene, from a limited number of
founders from the ANZ population, but
has since had little gene flow with the
ANZ population (Jorgensen et al., 2010).
Thus, although the two populations can
interbreed, they are thought to be largely
reproductively isolated (Jorgensen et al.,
2010).
In addition to genetic separation, the
NEP population is geographically
separated from other populations,
adheres to predictable seasonal
migratory routes, and exhibits strong
site fidelity within the NEP. As
discussed above, white sharks in the
NEP population range from Baja
California to the Bering Sea, and out to
Hawaii. Tagged white sharks from the
NEP population consistently used three
core areas within the northeastern and
central Pacific ocean: (a) The coastal
shelf waters of North America
(primarily from central California to
Baja California); (b) the slope and
offshore waters of the Hawaiian
archipelago; and (c) offshore waters
between California and Hawaii,
including an offshore habitat
approximately halfway between
California and Hawaii referred to as the
´
SOFA/white shark cafe, used primarily
by adults (Boustany et al., 2002;
Jorgensen et al., 2010; Domeier, 2012).
The individuals followed seasonal
migratory patterns, generally moving
offshore starting in winter and returning
to the California and Baja California
coast in the late summer (Jorgensen et
al., 2010; Domeier, 2012). Tagged
individuals from the NEP population
did not show any straying or spatial
overlap with the ANZ population
(Jorgensen et al., 2010). YOY and
juvenile white sharks also stay within
the geographic boundaries of the NEP
population, likely using nearshore,
shallow waters of the Southern
California Bight and Baja California as
nursery habitats, with adults likely
aggregating at sites off central California
and at Guadalupe Island (off Baja
California) to mate (Domeier, 2012).
Thus, the available information on
migratory behavior and habitat use
indicates that the NEP population is
geographically separated from other
white shark populations.
Second, the petitions state that the
NEP population is discrete because of
international governmental boundaries
within which differences in control of
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exploitation, management of habitat,
conservation status, or regulatory
mechanisms exist that are significant in
light of section 4(a)(1)(D) of the ESA
(i.e., the inadequacy of existing
regulatory mechanisms as a factor to
consider in determining whether a
species is endangered or threatened).
The petitions state that a large portion
of the NEP population’s habitat is
within U.S. waters, highlighting the
importance of U.S. protections for the
species. The petitions also argue that the
NEP population is discrete because it
ranges internationally into waters with
differing management regimes,
particularly when occupying offshore
habitats and visiting aggregation sites off
Baja California, where it may be subject
to exploitation by non-U.S. entities.
However, the Services’ DPS policy
states that a population may be
considered discrete if it is separated
from other populations by international
boundaries within which significant
differences in regulatory mechanisms
exist. That the NEP population crosses
these international boundaries actually
argues against considering this
population as discrete from other white
shark populations. Thus, the NEP
population is not considered discrete
based on this factor. Nevertheless, the
information available in the petitions
and in our files provides evidence
suggesting the NEP population may be
discrete based on both genetic and
spatial separation from other
populations.
Both petitions make the case that the
NEP population is significant to the
taxon. As described above, the NEP
population does not appear to overlap
spatially with other populations
(Jorgensen et al., 2010; Domeier, 2012;
Gubili et al., 2012). The petitions reason
that loss of this population would result
in a significant gap in the range of the
species because it is unlikely, given the
geographic separation of the NEP
population from other populations, that
sharks from other populations would
expand their distribution into the NEP’s
current habitats. The petitions also state
that the NEP population is genetically
differentiated from other white shark
populations, as described above. In
addition, the Oceana et al. petition
contends that the NEP population
occupies an ecological setting that is
unique to this species, because they are
the only population to occupy coastal
waters off California and the SOFA.
Overall, the information available in the
petitions and in our files suggests that
the NEP population of white shark may
be significant to the species. The Oceana
et al. petition also argues that great
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59585
white sharks play an important
ecological role that is essential for the
health of the NEP ecosystem, as a top
predator that regulates prey populations
(e.g., fish, other sharks, and pinnipeds).
We do not comment on the merit of this
statement, but note that in determining
whether a discrete population segment
is significant, the NMFS and USFWS
policy focuses on the biological and
ecological significance of the population
segment to the taxon, not to the
ecosystem.
Based on the above analysis, we
conclude that the information in the two
petitions and in our files suggests that
the NEP population of white shark may
qualify as a DPS under the discreteness
and significance requirements.
The Present or Threatened Destruction,
Modification, or Curtailment of the
Species’ Habitat or Range
Both petitions assert that habitat
degradation, largely associated with
increasing human activity, poses a
threat to the NEP population of white
shark, although the two petitions focus
on different sources of habitat
degradation. The Oceana et al. petition
briefly mentions that pollutant
discharge can degrade coastal
aggregation and nursery habitats,
whereas the WildEarth Guardians
petition goes into more detail on this
potential threat. The WildEarth
Guardians petition cites urban
stormwater runoff and point source
discharge as important sources of
pollutants (e.g., pesticides, fertilizers,
trace metals, synthetic organic
compounds, petroleum, and pathogens)
into the Southern California Bight
(DiGiacomo et al., 2004). The petition
states that these pollutants threaten
predators like white sharks, primarily
through effects on their prey. For
example, historical discharges of
organochlorines, such as DDT and PCBs,
into the Southern California Bight have
resulted in high levels of these
contaminants in local populations of
pinnipeds (Blasius and Goodmanlowe,
2008), one of the prey resources for
white sharks. Both petitions cite a
recent finding that young white sharks
sampled off California have high levels
of mercury, DDT, PCBs, and chlordanes
that could result in physiological
impairment (Mull et al., 2012). The
WildEarth Guardians petition briefly
states that water quality in areas off
Mexico where the NEP population
occurs may also be affected by
contaminants (Parks Watch, 2004).
The WildEarth Guardians petition
also suggests that the concentration of
marine debris in the North Pacific Gyre
(the ‘‘Great Pacific Garbage Patch’’) may
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have deleterious effects on offshore
habitats, including the SOFA. The main
concern expressed in the petition is the
concentration of plastic of various sizes
in the ‘‘Garbage Patch’’ (Algalita, 2009)
which could be ingested by white
sharks in the area either directly or
ingested by their prey. The petition also
suggests that accumulation of persistent
organic pollutants on the plastic
(Algalita, 2009) may pose another threat
to the health of white sharks. We note,
however, that it appears to be unclear
exactly what the adults (primarily
males) are preying on in the SOFA
(Jorgensen et al., 2010; Domeier, 2012)
because the area is devoid of the small
marine mammals typically preyed upon
by adult white sharks (Domeier, 2012).
Adults in the SOFA may be feeding on
squid or other species that target squid
(Domeier, 2012). Without specific
information about the extent to which
adults in the SOFA are feeding and
what they are feeding on, it is difficult
to evaluate the potential effects of
plastic marine debris on the NEP
population’s feeding habitat and prey
resources.
The Oceana et al. petition focuses on
two sources of habitat degradation: (1)
Decreased prey resources due to human
exploitation; and (2) the effects of ocean
acidification on the California Current
ecosystem. The WildEarth Guardians
petition briefly mentions that fisheries
activities in coastal areas may deplete
important prey resources for the NEP
population (CITES, 2004). The Oceana
et al. petition provides more detail,
stating that human exploitation
depleted populations of pinnipeds, an
important prey resource for adult white
sharks. The petition contends that
although pinniped populations are
currently increasing, they were depleted
for a long period of time and remain
below historical levels. We note that the
most recent stock assessments estimate
that harbor seals may be at carrying
capacity (NMFS, 2011a) and that
northern elephant seals have almost
reached their carrying capacity for pups
per year (NMFS, 2007). Population
trends have generally been increasing
since the 1980s or earlier for harbor
seals, California sea lions, and northern
elephant seals in California (NMFS,
2007; 2011a; 2011b). Thus, although
these prey resources may have been
limited in the past when pinniped
populations were at historical lows, the
populations have been increasing over
the last 30 years or more and may not
currently be limiting. For example, an
increased frequency of observed shark
attacks on prey off the South Farallon
Islands from 1983 to 1993 indicated a
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potential increase in the white shark
population at the islands, which may be
explained by increased recruitment of
younger white sharks supported by the
increase and stabilization of pinniped
prey resources over the 1970s and 1980s
(Pyle et al., 1996). Further analysis is
needed to evaluate what effect changes
in pinniped populations have had on
the status of white shark populations
over time. The petition also states that
there have been and continue to be
major commercial fisheries for most of
the other prey resources supporting
various life stages of white sharks (e.g.,
fish species, crustaceans, cephalopods;
Klimley, 1985; Ellis and McCosker,
1995). Again, further analysis is needed
to specifically evaluate the impacts of
these fisheries on prey resources for
white sharks.
The Oceana et al. petition also
contends that the effects of ocean
acidification could have negative
impacts on the marine food web within
the California Current ecosystem,
including on the NEP population of
white shark. The petition cites a model
simulation study which predicts that by
2050, the oceanic uptake of increased
atmospheric CO2 will lower the pH and
the saturation state of aragonite (a
mineral form of calcium carbonate, used
by calcifying organisms) in nearshore
waters of the California Current system
to levels well below the natural range
for this area (Gruber et al., 2012). The
petition states that these effects of ocean
acidification will have negative impacts
on fish species, referencing recent
studies showing that high CO2 and low
pH levels impair olfactory responses
and homing ability in clownfish
(Munday et al., 2009) and can lead to
cardiac failure in some fish species
(Ishimatsu et al., 2004). The petition
readily admits, however, that the
severity of effects on specific species is
uncertain. Some fish species may
experience metabolic responses to
elevated CO2 levels at the cellular level,
but are able to compensate for those
responses at the whole animal level,
making them less sensitive to the effects
of ocean acidification (Portner, 2008). In
addition, extrapolating specific effects at
the species levels to the overall
ecosystem (e.g., effects on prey
availability and predator-prey
interactions for top predators like white
sharks) is highly uncertain. The petition
also states that ocean acidification can
potentially affect marine mammals and
other marine life by reducing the sound
absorption of seawater and allowing
sound to travel further (Hester et al.,
2008). However, the petition does not
explain what the potential effects on
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marine mammals and other marine life
may be or how any such effects relate
to the degradation of white shark habitat
(e.g., the availability or abundance of
prey resources). The available
information is not sufficient to
determine if ocean acidification may be
threatening the habitat of the NEP
population of white shark such that
listing may be warranted.
We conclude that the information in
the petitions and in our files suggests
that habitat degradation associated with
pollutant discharge in the Southern
California Bight may be impacting the
health of the NEP population of white
shark. Human exploitation may have
impacted prey resources (e.g., pinnipeds
and fish and invertebrate species) in the
past; however, further analyses are
needed to evaluate the recent and
current impacts on prey resources. In
addition, the information provided on
the effects of marine debris in the North
Pacific Gyre or ocean acidification is
insufficient to evaluate whether these
factors may be threatening the habitat of
the NEP population of white shark such
that listing may be warranted.
Overutilization for Commercial,
Recreational, Scientific, or Educational
Purposes
Information from both petitions
suggests that a primary threat to the NEP
population of white shark is from
fisheries. The petitions cite information
on the effects of fisheries on white
sharks worldwide and within the NEP.
White sharks are harvested in targeted
fisheries and as bycatch and are highly
prized for their teeth, jaws, and fins.
White sharks are primarily caught
incidentally in commercial fisheries
using longlines, setlines, gillnets, trawls,
fish traps, and other gear (Compagno,
2001; Fowler et al., 2005; Lowe et al.,
2012; Santana-Morales et al., 2012). The
curious nature of white sharks makes
them more vulnerable to incidental
capture, and their high value and
negative reputation may contribute to
the killing of incidentally caught
individuals rather than being released
alive (Fowler et al., 2005). CITES
(2004a) estimated that low to mid
hundreds of white sharks are killed
annually as bycatch within each major
region of the species’ range. Targeted
sport and commercial fisheries for white
sharks also exist worldwide. Targeted
sports fisheries may either kill or release
sharks alive, but post-release mortality
is unknown. It is estimated that tens to
low hundreds of white sharks are killed
in sports fisheries worldwide each year
(CITES, 2004). Targeted commercial
fisheries for white sharks are thought to
be uncommon and opportunistic when
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aggregations are found, but the species’
site fidelity and tendency to aggregate in
predictable areas make it vulnerable to
over-exploitation (CITES, 2004).
Targeted commercial fisheries
worldwide may also kill tens to low
hundreds of white sharks each year
(CITES, 2004).
In the NEP Ocean, there is little
commercial fishing activity in the
SOFA, providing a potential refuge from
incidental capture for individuals when
they occupy this offshore area (Domeier,
2012). However, the lack of
international laws to protect great white
sharks in international waters is a
potential threat to the species (Domeier,
2012; discussed further under
‘‘Inadequacy of existing regulatory
mechanisms’’). White sharks are most
vulnerable to fisheries capture when
occupying nearshore aggregation or
nursery habitats, especially YOY and
juvenile stages (Domeier, 2012). Off
California, there have been no directed
fisheries for white sharks, but incidental
and targeted catch has occurred (Lowe
et al., 2012). An analysis of fisherydependent catch records for the
Southern California Bight from 1936 to
2009 found that the majority of the
reported white shark captures (where
size was indicated) were of YOY sharks
(60 percent), followed by juveniles (32
percent) and subadults/adults (8
percent); however, the proportion of
YOY sharks in the reported catch
increased to 77 percent after the
nearshore gillnet ban was implemented
in 1994 (Lowe et al., 2012). Commercial
entangling nets (81 percent) and
recreational hook-and-line fishing (8
percent) accounted for the majority of
the reported white shark captures (Lowe
et al., 2012). The number of reported
white shark captures in commercial
entangling nets has been 20 or less from
1985 through 2009, except in 1985
when 25 captures were reported (Lowe
et al., 2012). The analysis suggests that
the effects of incidental capture in
gillnet fisheries off California have
decreased compared to historical effects.
As gillnet fishing effort decreased from
the mid-1980s to mid-1990s, so did
reports of white shark captures (Lowe et
al., 2012). However, although gillnet
fishing effort remained stable or
decreased from the mid-1990s through
2009, reports of white shark captures
increased from 2005 through 2009
(Lowe et al., 2012). Increases in the
number of reported captures in the
gillnet fisheries since 2005, despite
stable or decreased effort, may be the
result of increased reporting of captures
and/or an increase in the abundance of
white sharks due to the nearshore
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gillnet ban and changes in offshore
gillnet regulations (Lowe et al., 2012).
Also, data from the Monterey Bay
Aquarium’s Juvenile White Shark
Tagging Program indicate that YOY and
juvenile white sharks have relatively
high post-release survival after being
caught in gillnet gear (Lowe et al., 2012).
Incidental catch of white sharks also
continues to occur off Baja California.
Incidental catch of 111 great white
sharks was reported from 1999 through
2010, consisting of YOY (79.8 percent)
and juvenile (20.2 percent) sharks
(Santana-Morales et al., 2012).
Incidental catch primarily occurred in
bottom gillnet gear (74.7 percent), but
also in drift gillnet (18 percent) and
artisanal seine net (4.5 percent) gear
(Santana-Morales et al., 2012).
The petitions assert that the
continued incidental catch of white
sharks poses a threat to the species,
because the removal of just a few
individuals could have a substantive
effect on the local population (Pyle et
al., 1996; Chapple, 2011). The petitions
also highlight the high value of white
shark teeth, jaws, and fins as trophies,
curios, and food, stating that this
provides a strong monetary incentive to
capture and keep white sharks (Clarke,
2004; Shivji et al., 2005; Clarke et al.,
2006).
We conclude that the petitions and
information in our files present
evidence that fisheries impacts continue
to affect white shark populations
worldwide and in the NEP, primarily
due to incidental capture in fisheries
and the potential for the high value of
great white shark teeth, jaws, and fins to
promote keeping incidentally caught
individuals rather than releasing them
back into the water. This information
suggests that fisheries impacts may be
affecting the continued existence of the
NEP population of white shark. To
further evaluate these effects, more
information is needed on fisheries
impacts specifically within the range of
the NEP population, particularly on the
capture of white sharks in fisheries in
offshore waters and the lethal and
sublethal effects of catch and release.
Disease or Predation
The WildEarth Guardians petition
asserts that the addition of mercury,
organochlorine contaminants, and other
pollutants to the ocean and the effects
of these pollutants on the NEP
population of white sharks may be
categorized as disease. The petition does
not provide any additional information
to support that disease is a factor
affecting the NEP population’s
continued existence such that listing
may be warranted. Thus, the available
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59587
information is insufficient to evaluate if
disease may be affecting the continued
existence of the NEP population of
white shark. The petition more
appropriately discusses pollutants and
their effects on the NEP population
under the habitat degradation and
‘‘other natural or manmade’’ factors.
Inadequacy of Existing Regulatory
Mechanisms
The petitions assert that the
inadequacy of existing Federal, state, or
international regulatory mechanisms
require that the NEP population of
white shark be listed under the ESA.
The petitions contend that although
Federal, state, and international
regulations exist to protect white sharks
from targeted capture in some areas,
these regulations are insufficient
because white sharks in the NEP
population are still vulnerable to
incidental capture throughout its range,
and to exploitation when in
international waters. In addition, the
WildEarth Guardians petition states that
existing regulations do not protect the
NEP population’s habitat and health
from threats such as habitat degradation,
pollution, and overfishing of prey
resources.
Within the United States, Federal and
state regulations to protect white sharks
vary. Currently, the retention of white
sharks in U.S. Federal waters in the
Pacific Ocean is prohibited under the
Highly Migratory Species Fishery
Management Plan. In California,
targeted capture of white sharks is
prohibited, but incidentally caught
white sharks may be retained under a
permit from the California Department
of Fish and Game for scientific or
educational purposes (14 CCR § 28.06).
In Oregon, all white sharks must be
released immediately if caught (ODFW,
2012). Washington and Hawaii do not
have specific fisheries regulations for
white shark. However, both Hawaii and
California passed bans making it
unlawful to possess, sell, offer for sale,
trade, or distribute shark fins, which
may provide some protection for white
sharks. The petitions argue that despite
these protections, the continued
incidental capture and mortality of even
small numbers of white sharks in U.S.
waters, particularly off California, can
have a large impact on the local
population, citing a study off the
Farallon Islands in which the removal of
four white sharks from the area in 1982
resulted in significantly fewer sightings
of shark attacks on pinnipeds than
expected in 1983 to 1985 (Pyle et al.,
1996). The petitions also suggest that
illegal fishing may be a problem in the
United States, citing cases of illegal
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fishing and sale of white shark teeth,
jaws, and fins in 2003 (CITES, 2004).
Outside of the United States,
protections for white sharks also vary.
In Mexico, catch and retention of white
sharks and the landing of shark fins
without carcasses has been banned
since 2006 (Lack and Sant, 2011),
although incidental capture continues to
´
˜
occur (Galvan-Magana et al., 2010;
Santana-Morales et al., 2012). In
Canada, there are no specific regulations
to protect white sharks, although a ban
on shark finning may provide some
protection (DFO, 2007). In international
waters, white sharks are protected under
CITES (Appendix II) and other
international agreements, including the
Convention on Migratory Species
(Appendix I and II) and the United
Nations Convention on the Law of the
Sea. However, the petitions contend that
these protections are not sufficient,
given continued trade in white shark
products due to poaching and variable
enforcement of regulations (CITES,
2004; Clarke, 2004; Shivji et al., 2005;
´
˜
Clarke et al., 2006; Galvan-Magana et
al., 2010; Jorgensen et al., 2010; Viegas,
2011).
Based on the information in the
petition and in our files as discussed
above, we conclude that existing
regulatory mechanisms may be
inadequate to address threats to the NEP
population of white shark. To further
evaluate the adequacy of existing
regulatory mechanisms, more
information is needed regarding the
level of illegal fishing and poaching in
U.S. and international waters.
Other Natural or Manmade Factors
The two petitions assert that other
natural or manmade factors may be
affecting the survival and recovery of
the NEP population of white shark,
including contaminant loads, negative
press, life history factors, small
population size, and the synergistic
effects of all of the threats facing the
population. Both petitions cite a study
conducted in the Southern California
Bight revealing mercury and
organochlorines (e.g., DDT, PCBs, and
chlordanes) in the tissues of juvenile
white sharks at levels that may result in
physiological impairment (Mull et al.,
2012). Young white sharks are likely
bioaccumulating these contaminants
(likely from historical discharges in the
Southern California Bight) when feeding
on prey resources in the area (Blasius
and Goodmanlowe, 2008; Mull et al.,
2012). The WildEarth Guardian petition
also cites negative media attention as a
threat to white sharks, especially when
shark attacks on humans occur, because
this generates general paranoia and
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encourages targeting of the species for
sport or trophy hunting (IUCN, 2009).
The WildEarth Guardians petition
asserts that natural factors, including
the species’ life history characteristics
and small population size, also increase
the extinction risk of the NEP
population of white shark, particularly
when considered in combination with
other threats to the species. The petition
states that the species’ life history
characteristics (e.g., slow growth, late
maturation, long-life, long generation
time, small litter size, and low
reproductive capacity) make it
susceptible to extinction when faced
with population declines and
continuing threats (Withgott and
Brennan, 2007). The petition also
contends that the small estimated
population size (e.g., approximately 340
subadults and adults in the NEP
population; Chapple et al., 2011; SosaNishizaki et al., 2012) makes the
population highly susceptible to
extinction due to a stochastic event
(Brook et al., 2008). We note, however,
that this estimate of abundance is based
on studies of individuals surveyed in
aggregation sites off central California
and Guadalupe Island, and do not
include YOY and juveniles. Also,
without information on the historical
abundance of the NEP population, it is
difficult to assess what this estimated
population size means for the
persistence of the population. The low
estimated abundance of the population
may be the result of anthropogenic
pressures on the population or a
naturally low carrying capacity (the NEP
population is thought to have been
established by a limited number of
founders from the ANZ population;
Jorgensen et al., 2010) (Chapple et al.,
2011). Catch ratios of white sharks to all
shark species off the U.S. west coast
from 1965 (1:67) to 1983 (1:210) suggest
a potential decline in abundance (Casey
and Pratt, 1985, cited in Fowler et al.,
2005). However, recent increases in the
incidental capture of white sharks in
gillnet fisheries off California, despite
stable or decreasing fishing effort,
suggest that the population may be
increasing (Lowe et al., 2012). In
addition, an increased frequency of
observed white shark attacks on
pinnipeds off the South Farallon Islands
over time indicates an increase in the
shark population at the islands (Pyle et
al., 1996; Pyle et al., 2003). Thus, it is
difficult at this time to determine
population trends and to evaluate how
the estimated size of the NEP
population relates to the population’s
extinction risk.
Overall, the petition and information
in our files suggest that effects from
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bioaccumulation of contaminants and
negative media attention, coupled with
the life history characteristics of white
sharks, may be affecting the survival
and recovery of the NEP population.
More specific information is needed,
however, to assess population trends
and to evaluate the population’s
estimated abundance in terms of the
potential effects on the population’s
survival and recovery.
Summary of Section 4(a)(1) Factors
We conclude that the petition
presents substantial scientific or
commercial information indicating that
multiple section 4(a)(1) factors, as
discussed above, may be causing or
contributing to an increased risk of
extinction for the NEP population of
white shark.
Petition Finding
After reviewing the information
contained in both petitions, as well as
information readily available in our
files, we conclude the petitions present
substantial scientific information
indicating the petitioned action of
listing the NEP population of white
shark as a threatened or endangered
DPS may be warranted. Therefore, in
accordance with section 4(b)(3)(A) of
the ESA and NMFS’ implementing
regulations (50 CFR 424.14(b)(3)), we
will commence a status review of the
species. During the status review, we
will determine whether the population
identified by the petitioners meets the
DPS policy’s criteria, and if so, whether
the population is in danger of extinction
(endangered) or likely to become so
within the foreseeable future
(threatened) throughout all or a
significant portion of its range. We now
initiate this review, and thus, the
northeastern Pacific Ocean population
of white shark is considered to be a
candidate species (50 CFR 424.15(b)).
Within 12 months of the receipt of the
WildEarth Guardians petition (June 25,
2013), we will make a finding as to
whether listing the species as
endangered or threatened is warranted
as required by section 4(b)(3)(B) of the
ESA. If listing the species is warranted,
we will publish a proposed rule and
solicit public comments before
developing and publishing a final rule.
Information Solicited
To ensure that the status review is
based on the best available scientific
and commercial data, we are soliciting
information relevant to whether the NEP
Ocean population of white sharks is a
DPS and whether it is threatened or
endangered. Specifically, we are
soliciting published and unpublished
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information in the following areas: (1)
Population structure information in the
Pacific Ocean, such as genetics data;
particularly any unpublished
information; (2) migratory and behavior
patterns in the NEP Ocean, particularly
any unpublished information; (3) life
history and ecology, particularly any
unpublished information; (4) historical
and current distribution and abundance
of this species throughout the NEP
Ocean; (5) historical and current
population trends in the NEP Ocean; (6)
historical and current data on
commercial and recreational fisheries
directed at white sharks in the NEP
Ocean, including Mexican waters; (7)
historical and current data on white
shark bycatch and retention in
commercial and recreational fisheries in
the NEP Ocean, including Mexican
waters; (8) data on the trade of white
shark products, including fins, jaws,
and teeth in the NEP Ocean, including
Mexico; (9) data or other information on
encounter rates with white sharks
through ecotourism operations and
sightings data, and long-term records of
white shark attacks, wounds or scaring
of marine mammals; (10) adverse
impacts related to coastal habitat
degradation and the health of white
sharks, including, but not limited to,
impacts related to discharge of
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pollutants, marine debris, or ocean
acidification; (11) any current or
planned activities that may adversely
impact the species; (12) ongoing or
planned efforts to protect and restore
the species and their habitats; and (12)
management, regulatory, and
enforcement information.
We also request information on
critical habitat for the NEP Ocean
population of white sharks. Specifically,
we request information on the physical
and biological habitat features that are
essential to the conservation of the
species and identification of habitat
areas that include these essential
physical and biological features.
Essential features include, but are not
limited to: (1) Space for individual and
population growth and for normal
behavior; (2) food, water, air, light,
minerals, or other nutritional or
physiological requirements; (3) cover or
shelter; (4) sites for reproduction and
development of offspring; and (5)
habitats that are protected from
disturbance or are representative of the
historical, geographical, and ecological
distributions of the species (50 CFR
424.12). For habitat areas potentially
qualifying as critical habitat, we request
information describing: (1) The
activities that affect the habitat areas or
could be affected by the designation;
and (2) the economic impacts, impacts
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59589
to national security, or other relevant
impacts of additional requirements of
management measures likely to result
from the designation.
We request that all information be
accompanied by: (1) Supporting
documentation such as maps, raw data
with associated documentation,
bibliographic references, or reprints of
pertinent publications; and (2) the
submitter’s name, mailing address,
email address, and any association,
institution, or business that the person
represents.
References Cited
A complete list of references is
available upon request from the NMFS
Southwest Regional Office (see
ADDRESSES).
Authority
The authority for this action is the
Endangered Species Act of 1973, as
amended (16 U.S.C. 1531 et seq.).
Dated: September 25, 2012.
Alan D. Risenhoover,
Director, Office of Sustainable Fisheries,
performing the functions and duties of the
Deputy Assistant Administrator for
Regulatory Programs, National Marine
Fisheries Service.
[FR Doc. 2012–23963 Filed 9–27–12; 8:45 am]
BILLING CODE 3510–22–P
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Agencies
- DEPARTMENT OF COMMERCE
- National Ocean and Atmospheric Administration
[Federal Register Volume 77, Number 189 (Friday, September 28, 2012)]
[Proposed Rules]
[Pages 59582-59589]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2012-23963]
[[Page 59582]]
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DEPARTMENT OF COMMERCE
National Ocean and Atmospheric Administration
50 CFR Parts 223 and 224
[Docket No. 120807313-2313-01]
RIN 0648-XC154
Endangered and Threatened Wildlife; 90-Day Finding on Petitions
To List the Northeastern Pacific Ocean Distinct Population Segment of
Great White Shark as Threatened or Endangered Under the Endangered
Species Act
AGENCY: National Marine Fisheries Service (NMFS), National Oceanic and
Atmospheric Administration (NOAA), Commerce.
ACTION: 90-day petition finding, request for information, and
initiation of status review.
-----------------------------------------------------------------------
SUMMARY: We, NMFS, announce a 90-day finding on two petitions received
to list the northeastern Pacific Ocean population of great white shark
(Carcharodon carcharias) as a threatened or endangered distinct
population segment (DPS) under the Endangered Species Act (ESA) and to
designate critical habitat concurrently with the listing. We find that
the petitions and information in our files present substantial
scientific or commercial information indicating that the petitioned
action may be warranted. We will conduct a status review of the species
to determine if the petitioned action is warranted. To ensure that the
status review is comprehensive, we are soliciting scientific and
commercial information pertaining to this species from any interested
party.
DATES: Information and comments on the subject action must be received
by November 27, 2012.
ADDRESSES: You may submit comments, information, or data, identified by
``NOAA-NMFS-2012-0176'' by any one of the following methods:
Electronic Submissions: Submit all electronic comments via
the Federal eRulemaking Portal https://www.regulations.gov. To submit
comments via the e-Rulemaking Portal, first click the ``submit a
comment'' icon, then enter ``NOAA-NMFS-2012-0176'' in the keyword
search. Locate the document you wish to comment on from the resulting
list and click on the ``Submit a Comment'' icon on the right of that
line.
Mail or hand-delivery: Protected Resources Division,
Southwest Region, NMFS, 501 West Ocean Blvd., Suite 4200, Long Beach,
CA 90802-4213.
Instructions: All comments received are a part of the public record
and may be posted to https://www.regulations.gov without change. All
personally identifiable information (for example, name, address, etc.)
voluntarily submitted by the commenter may be publicly accessible. Do
not submit confidential business information or other information you
wish to protect from public disclosure. NMFS will accept anonymous
comments. Attachments to electronic comments will be accepted in
Microsoft Word, Excel, Corel WordPerfect, or Adobe PDF file formats
only.
FOR FURTHER INFORMATION CONTACT: Craig Wingert, NMFS, Southwest Region,
(562) 980-4021; or Marta Nammack, NMFS, Office of Protected Resources,
(301) 427-8469.
SUPPLEMENTARY INFORMATION:
Background
On June 25, 2012, we received a petition from WildEarth Guardians
to list the northeastern Pacific Ocean DPS of great white shark
(Carcharodon carcharias) as threatened or endangered under the ESA. The
petitioners also requested that critical habitat be designated for this
DPS under the ESA. On August 13, 2012, we received a second petition,
filed jointly by Oceana, Center for Biological Diversity (CBD), and
Shark Stewards, to list the northeastern Pacific Ocean DPS of white
shark (another common name for the great white shark) under the ESA and
designate critical habitat. Both petitions bring forth much of the same
or related factual information on the biology and ecology of great
white sharks, and raise several identical or similar issues related to
potential factors affecting this species. As a result, we are
considering both petitions simultaneously in this 90-day finding.
Copies of the petitions are available upon request (see ADDRESSES,
above).
ESA Statutory, Regulatory, and Policy Provisions and Evaluation
Framework
Section 4(b)(3)(A) of the ESA of 1973, as amended (16 U.S.C. 1531
et seq.), requires, to the maximum extent practicable, that within 90
days of receipt of a petition to list a species as threatened or
endangered, the Secretary of Commerce make a finding on whether that
petition presents substantial scientific or commercial information
indicating that the petitioned action may be warranted, and to promptly
publish such finding in the Federal Register (16 U.S.C. 1533(b)(3)(A)).
When it is found that substantial scientific or commercial information
in a petition indicates the petitioned action may be warranted (a
``positive 90-day finding''), we are required to promptly commence a
review of the status of the species concerned during which we will
conduct a comprehensive review of the best available scientific and
commercial information. In such cases, we conclude the status review
with a finding published in the Federal Register as to whether or not
the petitioned action is warranted within 12 months of receipt of the
petition. Because the finding at the 12-month stage is based on a
thorough review of the available information, as compared to the more
limited scope of review at the 90-day stage, a ``may be warranted''
finding does not prejudge the outcome of the status review.
Under the ESA, a listing determination may address a species, which
is defined to also include any subspecies and, for vertebrate species,
any DPS which interbreeds when mature (16 U.S.C. 1532(16)). A joint
NMFS-U.S. Fish and Wildlife Service (USFWS) (jointly, ``the Services'')
policy clarifies the agencies' interpretation of the phrase ``distinct
population segment'' for the purposes of listing, delisting, and
reclassifying a species under the ESA (61 FR 4722; February 7, 1996). A
species, subspecies, or DPS is ``endangered'' if it is in danger of
extinction throughout all or a significant portion of its range, and
``threatened'' if it is likely to become endangered within the
foreseeable future throughout all or a significant portion of its range
(16 U.S.C. 1532(6) and (20)). Pursuant to the ESA and our implementing
regulations, we determine whether species are threatened or endangered
based on any one or a combination of the following factors: (1) The
present or threatened destruction, modification, or curtailment of its
habitat or range; (2) overutilization for commercial, recreational,
scientific, or educational purposes; (3) disease or predation; (4) the
inadequacy of existing regulatory mechanisms; and (5) any other natural
or manmade factors affecting the species' continued existence (16
U.S.C. 1533(a)(1), 50 CFR 424.11(c)).
ESA implementing regulations define ``substantial information'' in
the context of reviewing a petition to list, delist, or reclassify a
species as the amount of information that would lead a reasonable
person to believe that the measure proposed in the petition may be
warranted (50 CFR 424.14(b)). In evaluating whether substantial
information is contained in a petition, the Secretary must consider
whether the petition: (1) Clearly indicates the administrative measure
recommended
[[Page 59583]]
and gives the scientific and any common name of the species involved;
(2) contains detailed narrative justification for the recommended
measure, describing, based on available information, past and present
numbers and distribution of the species involved and any threats faced
by the species; (3) provides information regarding the status of the
species over all or a significant portion of its range; and (4) is
accompanied by the appropriate supporting documentation in the form of
bibliographic references, reprints of pertinent publications, copies of
reports or letters from authorities, and maps (50 CFR 424.14(b)(2)).
Judicial decisions have clarified the appropriate scope and
limitations of the Services' review of petitions at the 90-day finding
stage, in making a determination that a petitioned action ``may be''
warranted. As a general matter, these decisions hold that a petition
need not establish a ``strong likelihood'' or a ``high probability''
that a species is either threatened or endangered to support a positive
90-day finding.
We evaluate the petitioners' request based upon the information in
the petition including its references and the information readily
available in our files. We do not conduct additional research and we do
not solicit information from parties outside the agency to help us in
evaluating the petition. We will accept the petitioners' sources and
characterizations of the information presented if they appear to be
based on accepted scientific principles, unless we have specific
information in our files indicating the petition's information is
incorrect, unreliable, obsolete, or otherwise irrelevant to the
requested action. Information that is susceptible to more than one
interpretation or that is contradicted by other available information
will not be dismissed at the 90-day finding stage, so long as it is
reliable and a reasonable person would conclude it supports the
petitioners' assertions. In other words, conclusive information
indicating the species may meet the ESA's requirements for listing is
not required to make a positive 90-day finding. We will not conclude
that a lack of specific information negates a positive 90-day finding
if a reasonable person would conclude that the uncertainty from the
lack of information suggests an extinction risk of concern for the
species at issue.
To make a 90-day finding on a petition to list a species, we
evaluate whether the petition presents substantial scientific or
commercial information indicating the subject species may be either
threatened or endangered, as defined by the ESA. First, we evaluate
whether the information presented in the petition, along with the
information readily available in our files, indicates that the
petitioned entity constitutes a ``species'' eligible for listing under
the ESA. Next, we evaluate whether the information indicates that the
species faces an extinction risk that is cause for concern; this may be
indicated in information expressly discussing the species' status and
trends, or in information describing impacts and threats to the
species. We evaluate any information on specific demographic factors
pertinent to evaluating extinction risk for the species (e.g.,
population abundance and trends, productivity, spatial structure, age
structure, sex ratio, diversity, current and historical range, habitat
integrity or fragmentation), and the potential contribution of
identified demographic risks to extinction risk for the species. We
then evaluate the potential links between these demographic risks and
the causative impacts and threats identified in section 4(a)(1).
Information presented on impacts or threats should be specific to
the species and should reasonably suggest that one or more of these
factors may be operative threats that act or have acted on the species
to the point that it may warrant protection under the ESA. Broad
statements about generalized threats to the species, or identification
of factors that could negatively impact a species, do not constitute
substantial information indicating that listing may be warranted. We
look for information indicating that not only is the particular species
exposed to a factor, but that the species may be responding in a
negative fashion; then we assess the potential significance of that
negative response.
Many petitions identify risk classifications made by non-
governmental organizations, such as the International Union on the
Conservation of Nature (IUCN), the American Fisheries Society, or
NatureServe, as evidence of extinction risk for a species. Risk
classifications by other organizations or made under other Federal or
state statutes may be informative, but the classification alone does
not provide the rationale for a positive 90-day finding under the ESA.
For example, as explained by NatureServe, their assessments of a
species' conservation status do ``not constitute a recommendation by
NatureServe for listing under the U.S. Endangered Species Act'' because
NatureServe assessments ``have different criteria, evidence
requirements, purposes and taxonomic coverage than government lists of
endangered and threatened species, and therefore these two types of
lists should not be expected to coincide'' (https://www.natureserve.org/prodServices/statusAssessment.jsp). Thus, when a petition cites such
classifications, we will evaluate the source of information that the
classification is based upon in light of the standards on extinction
risk and impacts or threats discussed above.
Distribution and Life History of the Great White Shark
The great white shark (also known as ``white shark'') is a
circumglobal species that resides primarily in temperate and sub-
tropical waters (Compagno et al., 1997; Domeier and Nasby-Lucas, 2006;
Domeier et al., 2012). White sharks commonly inhabit coastal and
continental shelf waters, although they have been observed entering
marine bays, estuaries, lagoons, and harbors (Compagno et al., 1997).
Recent studies suggest that these sharks also spend considerable amount
of time in open ocean habitats thousands of kilometers from shore
(Domeier, 2012). Areas likely to attract adult white sharks include
coastal waters adjacent to pinniped colonies or haulout sites, as these
are favored prey species (Klimley et al., 1996; Hussey et al., 2012).
Known prey of white sharks also includes a wide range of other species
from smaller demersal fish, such as rockfish, to giant pelagic species,
such as tuna and swordfish, as well as sea turtles, seabirds,
cetaceans, and other species of sharks (Fergusson, 1996; Long and
Jones, 1996; Wilson and Patyten, 2008; IUCN, 2009; Santana-Morales et
al., 2012). White sharks are recognized as apex predators throughout
the oceanic and coastal marine environments where they occur, and may
play an important role in ecosystem balance and population control for
a number of other marine species (Myers et al., 2007; Wilson and
Patyten, 2008). White sharks demonstrate the ability to undertake
transoceanic migrations to specific locations in patterns that appear
to be predictable (Boustany et al., 2002; Jorgensen et al., 2010;
Chapple et al., 2011; Domeier, 2012).
Great white sharks are distinguished by their stout spindle-shaped
body, moderately long and bluntly conical snout, five long gill slits,
large falcate first dorsal fin with free rear tip located over the
pectoral inner margins, pivoting second dorsal and anal fins, white
ventral body color, and lack of any secondary keels on the base of the
caudal fin. The teeth are large, flat, and triangular shaped, with
blade-like serrations, although teeth in the rear of
[[Page 59584]]
the mouth get progressively smaller and sometimes lack serration,
especially in younger sharks (Compagno et al., 1997; FAO, 2012). The
maximum size of this species has not been established, but has been
estimated at about 6 m (19 ft), and possibly up to 6.4 m (21 ft), or
more (Cailliet et al., 1985; Wilson and Patyten, 2008; IUCN, 2009).
Estimated weight of the largest individuals is nearly 3,000 kg (6,600
lbs) (Cailliet et al., 1985; Anderson et al., 2011).
Available information on the general life history pattern of white
sharks suggests that females mature at about 12-14 years of age, and
about 4-5 m (13-16 ft) in length. Males mature at 9-10 years old, and
about 3.5-4.1 m (11.5-13.5 ft) in length (Compagno et al., 1997). It is
believed that females give birth at 2 or 3-year intervals to litters of
2-10 pups that are 1-1.5 m (3.3-4.9 ft) in length after a 12-22 month
gestation (Francis, 1996; Wilson and Patyten, 2008; Domeier, 2012).
Embryos are oophagus, meaning they consume and store yolk in their
stomachs (Francis, 1996; Uchida et al., 1996), and viviparous (live)
birth of pups likely occurs sometime between May and October (Domeier,
2012). Specific knowledge of pup survival rates is not available, but
is estimated to be low (CITES, 2004).
Primary concentrations of white sharks occur in South Africa,
Australia and New Zealand, and the northeastern Pacific Ocean, with
other white sharks observed in the north Atlantic and the Mediterranean
(Boustany et al., 2002; Domeier and Nasby-Lucas, 2006; Weng et al.,
2007; Jorgensen et al., 2010). Genetic and migration studies provide
evidence that these may represent separate populations (Jorgensen et
al., 2010). Mitochondrial DNA suggests at least three matrilineal
populations: South Africa/northwest Atlantic; southwest Pacific; and
northeastern Pacific (Gubili et al., 2012). Although the southwestern
Pacific and northeastern Pacific populations could potentially
interbreed, the genetic sampling indicates that these two populations
are largely reproductively isolated. It has been suggested that the
northeastern Pacific population was founded by relatively few sharks
within the last 200,000 years, and hasn't mixed with other shark
populations near Australia or South Africa since (Hance, 2009;
Jorgensen et al., 2010).
White sharks in the northeastern Pacific Ocean have been observed
from Baja California to the Bering Sea (Kato, 1965; COSEWIC, 2006) and
offshore out to Hawaii. Using satellite and acoustic telemetry,
researchers have followed movements of white sharks in the northeastern
Pacific Ocean and discovered patterns of site fidelity and repeated
homing in structured seasonal migrations, including fixed destinations,
schedules, and routes (Boustany et al., 2002; Jorgensen et al., 2010).
As a result, three core areas have been identified in the central and
northeastern Pacific: (1) North American shelf waters; (2) slope and
offshore waters of Hawaii; and (3) an area between the North American
coast and Hawaii termed the ``white shark caf[eacute]'' or Shared
Offshore Foraging Area (SOFA) (Jorgensen et al., 2010; Anderson et al.,
2011; Domeier, 2012). Each winter, great white sharks leave coastal
aggregation sites off of central California (Farallon Islands/
A[ntilde]o Nuevo/Point Reyes) and migrate 2000-5000 km offshore to
subtropical and tropical pelagic habitats, returning to coastal
aggregation sites in late summer. Site fidelity in North American
coastal hotspots has also been documented using photo-identification
(Jorgensen et al., 2010; Chapple et al., 2011; Sosa-Nishizaki et al.,
2012). Guadalupe Island, located 250 miles off the coast of Baja
California, Mexico, is also a preferred aggregation site for adults
(Sosa-Nishizaki et al., 2012). Adult males annually migrate from
preferred aggregation sites to the SOFA/white shark caf[eacute].
Females have been observed to migrate biennially between preferred
aggregation sites and the area surrounding the SOFA/white shark
caf[eacute], usually after males have returned to coastal aggregation
sites (Domeier, 2012).
The coastal areas of southern California and Baja California,
Mexico, appear to be important nursery areas hosting large
concentrations of young-of-the-year (YOY) and juvenile great white
sharks (Dewar et al. 2004; Weng et al., 2007; Galv[aacute]n-
Maga[ntilde]a et al., 2011; Domeier, 2012; Santana-Morales et al.,
2012). Information gained from the records of white shark bycatch in
California and Baja fisheries, including gillnet, seine-net, and hook
and line fisheries (Lowe et al., 2012; Santana-Morales et al., 2012),
along with relatively consistent reporting of juvenile white shark
observations along the southern California coast, lend support to the
assertion that this area is important developmental habitat for white
sharks before they mature into larger adults. Estimates of abundance
have not been available historically, but recent studies have suggested
the population size at two known aggregation sites (Farallon Islands/
Central California and Guadalupe Island) in the northeastern Pacific
Ocean is around 340 sub-adults and adults (Chapple et al., 2011; Sosa-
Nishizaki et al., 2012).
Analysis of the Petitions and Information Readily Available in NMFS
Files
The two petitions request the same action, to list the northeastern
Pacific Ocean (NEP) DPS of great white shark (or white shark) as
endangered or threatened under the ESA and to designate critical
habitat for the DPS. Therefore, we evaluated the information provided
in both petitions and readily available in our files to determine if
the petitions presented substantial scientific or commercial
information indicating that the petitioned action may be warranted.
Both petitions contain information on the species, including the
taxonomy, species description, geographic distribution, habitat,
population status and trends, and factors contributing to the species'
decline. Both petitions state that a primary threat to the NEP
population of white shark is exploitation by fishing (historical and
current) and bycatch in fisheries. Both petitions also assert that the
lack of adequate regulatory protection worldwide, bioaccumulation of
contaminants, and habitat degradation, as well as the species'
biological constraints, increase the susceptibility of the NEP
population of white shark to extinction.
According to both petitions, the NEP population of white shark
qualifies as a DPS because the NEP population is both discrete and
significant, as defined under the Services' DPS policy (61 FR 4722;
February 7, 1996). The WildEarth Guardians petition asserts that all of
the five causal factors in section 4(a)(1) of the ESA are adversely
affecting the continued existence of the NEP population, whereas the
Oceana et al. petition does not discuss disease and predation as a
factor that is adversely affecting the NEP population. In the following
sections, we analyze the information presented by the petitions and in
our files on the qualification of the NEP population of white shark as
a DPS and the specific ESA section 4(a)(1) factors affecting the
population's risk of extinction.
Qualification of Northeastern Pacific Ocean Population as a DPS
Both petitions assert that the NEP population of white shark
qualifies as a DPS, because it is both a discrete and significant
population segment of the species, as defined in the NMFS and USFWS
policy on DPSs (61 FR 4722; February 7, 1996). First, the petitions
state that the NEP population is discrete based on both genetic and
spatial
[[Page 59585]]
separation from other populations of white shark. Genetic analyses
indicate that the NEP population of white sharks is similar to and
descended from the Australian/New Zealand (ANZ) population (Jorgensen
et al., 2010; Gubili et al., 2012). The NEP population was likely
established during the Late Pleistocene, from a limited number of
founders from the ANZ population, but has since had little gene flow
with the ANZ population (Jorgensen et al., 2010). Thus, although the
two populations can interbreed, they are thought to be largely
reproductively isolated (Jorgensen et al., 2010).
In addition to genetic separation, the NEP population is
geographically separated from other populations, adheres to predictable
seasonal migratory routes, and exhibits strong site fidelity within the
NEP. As discussed above, white sharks in the NEP population range from
Baja California to the Bering Sea, and out to Hawaii. Tagged white
sharks from the NEP population consistently used three core areas
within the northeastern and central Pacific ocean: (a) The coastal
shelf waters of North America (primarily from central California to
Baja California); (b) the slope and offshore waters of the Hawaiian
archipelago; and (c) offshore waters between California and Hawaii,
including an offshore habitat approximately halfway between California
and Hawaii referred to as the SOFA/white shark caf[eacute], used
primarily by adults (Boustany et al., 2002; Jorgensen et al., 2010;
Domeier, 2012). The individuals followed seasonal migratory patterns,
generally moving offshore starting in winter and returning to the
California and Baja California coast in the late summer (Jorgensen et
al., 2010; Domeier, 2012). Tagged individuals from the NEP population
did not show any straying or spatial overlap with the ANZ population
(Jorgensen et al., 2010). YOY and juvenile white sharks also stay
within the geographic boundaries of the NEP population, likely using
nearshore, shallow waters of the Southern California Bight and Baja
California as nursery habitats, with adults likely aggregating at sites
off central California and at Guadalupe Island (off Baja California) to
mate (Domeier, 2012). Thus, the available information on migratory
behavior and habitat use indicates that the NEP population is
geographically separated from other white shark populations.
Second, the petitions state that the NEP population is discrete
because of international governmental boundaries within which
differences in control of exploitation, management of habitat,
conservation status, or regulatory mechanisms exist that are
significant in light of section 4(a)(1)(D) of the ESA (i.e., the
inadequacy of existing regulatory mechanisms as a factor to consider in
determining whether a species is endangered or threatened). The
petitions state that a large portion of the NEP population's habitat is
within U.S. waters, highlighting the importance of U.S. protections for
the species. The petitions also argue that the NEP population is
discrete because it ranges internationally into waters with differing
management regimes, particularly when occupying offshore habitats and
visiting aggregation sites off Baja California, where it may be subject
to exploitation by non-U.S. entities. However, the Services' DPS policy
states that a population may be considered discrete if it is separated
from other populations by international boundaries within which
significant differences in regulatory mechanisms exist. That the NEP
population crosses these international boundaries actually argues
against considering this population as discrete from other white shark
populations. Thus, the NEP population is not considered discrete based
on this factor. Nevertheless, the information available in the
petitions and in our files provides evidence suggesting the NEP
population may be discrete based on both genetic and spatial separation
from other populations.
Both petitions make the case that the NEP population is significant
to the taxon. As described above, the NEP population does not appear to
overlap spatially with other populations (Jorgensen et al., 2010;
Domeier, 2012; Gubili et al., 2012). The petitions reason that loss of
this population would result in a significant gap in the range of the
species because it is unlikely, given the geographic separation of the
NEP population from other populations, that sharks from other
populations would expand their distribution into the NEP's current
habitats. The petitions also state that the NEP population is
genetically differentiated from other white shark populations, as
described above. In addition, the Oceana et al. petition contends that
the NEP population occupies an ecological setting that is unique to
this species, because they are the only population to occupy coastal
waters off California and the SOFA. Overall, the information available
in the petitions and in our files suggests that the NEP population of
white shark may be significant to the species. The Oceana et al.
petition also argues that great white sharks play an important
ecological role that is essential for the health of the NEP ecosystem,
as a top predator that regulates prey populations (e.g., fish, other
sharks, and pinnipeds). We do not comment on the merit of this
statement, but note that in determining whether a discrete population
segment is significant, the NMFS and USFWS policy focuses on the
biological and ecological significance of the population segment to the
taxon, not to the ecosystem.
Based on the above analysis, we conclude that the information in
the two petitions and in our files suggests that the NEP population of
white shark may qualify as a DPS under the discreteness and
significance requirements.
The Present or Threatened Destruction, Modification, or Curtailment of
the Species' Habitat or Range
Both petitions assert that habitat degradation, largely associated
with increasing human activity, poses a threat to the NEP population of
white shark, although the two petitions focus on different sources of
habitat degradation. The Oceana et al. petition briefly mentions that
pollutant discharge can degrade coastal aggregation and nursery
habitats, whereas the WildEarth Guardians petition goes into more
detail on this potential threat. The WildEarth Guardians petition cites
urban stormwater runoff and point source discharge as important sources
of pollutants (e.g., pesticides, fertilizers, trace metals, synthetic
organic compounds, petroleum, and pathogens) into the Southern
California Bight (DiGiacomo et al., 2004). The petition states that
these pollutants threaten predators like white sharks, primarily
through effects on their prey. For example, historical discharges of
organochlorines, such as DDT and PCBs, into the Southern California
Bight have resulted in high levels of these contaminants in local
populations of pinnipeds (Blasius and Goodmanlowe, 2008), one of the
prey resources for white sharks. Both petitions cite a recent finding
that young white sharks sampled off California have high levels of
mercury, DDT, PCBs, and chlordanes that could result in physiological
impairment (Mull et al., 2012). The WildEarth Guardians petition
briefly states that water quality in areas off Mexico where the NEP
population occurs may also be affected by contaminants (Parks Watch,
2004).
The WildEarth Guardians petition also suggests that the
concentration of marine debris in the North Pacific Gyre (the ``Great
Pacific Garbage Patch'') may
[[Page 59586]]
have deleterious effects on offshore habitats, including the SOFA. The
main concern expressed in the petition is the concentration of plastic
of various sizes in the ``Garbage Patch'' (Algalita, 2009) which could
be ingested by white sharks in the area either directly or ingested by
their prey. The petition also suggests that accumulation of persistent
organic pollutants on the plastic (Algalita, 2009) may pose another
threat to the health of white sharks. We note, however, that it appears
to be unclear exactly what the adults (primarily males) are preying on
in the SOFA (Jorgensen et al., 2010; Domeier, 2012) because the area is
devoid of the small marine mammals typically preyed upon by adult white
sharks (Domeier, 2012). Adults in the SOFA may be feeding on squid or
other species that target squid (Domeier, 2012). Without specific
information about the extent to which adults in the SOFA are feeding
and what they are feeding on, it is difficult to evaluate the potential
effects of plastic marine debris on the NEP population's feeding
habitat and prey resources.
The Oceana et al. petition focuses on two sources of habitat
degradation: (1) Decreased prey resources due to human exploitation;
and (2) the effects of ocean acidification on the California Current
ecosystem. The WildEarth Guardians petition briefly mentions that
fisheries activities in coastal areas may deplete important prey
resources for the NEP population (CITES, 2004). The Oceana et al.
petition provides more detail, stating that human exploitation depleted
populations of pinnipeds, an important prey resource for adult white
sharks. The petition contends that although pinniped populations are
currently increasing, they were depleted for a long period of time and
remain below historical levels. We note that the most recent stock
assessments estimate that harbor seals may be at carrying capacity
(NMFS, 2011a) and that northern elephant seals have almost reached
their carrying capacity for pups per year (NMFS, 2007). Population
trends have generally been increasing since the 1980s or earlier for
harbor seals, California sea lions, and northern elephant seals in
California (NMFS, 2007; 2011a; 2011b). Thus, although these prey
resources may have been limited in the past when pinniped populations
were at historical lows, the populations have been increasing over the
last 30 years or more and may not currently be limiting. For example,
an increased frequency of observed shark attacks on prey off the South
Farallon Islands from 1983 to 1993 indicated a potential increase in
the white shark population at the islands, which may be explained by
increased recruitment of younger white sharks supported by the increase
and stabilization of pinniped prey resources over the 1970s and 1980s
(Pyle et al., 1996). Further analysis is needed to evaluate what effect
changes in pinniped populations have had on the status of white shark
populations over time. The petition also states that there have been
and continue to be major commercial fisheries for most of the other
prey resources supporting various life stages of white sharks (e.g.,
fish species, crustaceans, cephalopods; Klimley, 1985; Ellis and
McCosker, 1995). Again, further analysis is needed to specifically
evaluate the impacts of these fisheries on prey resources for white
sharks.
The Oceana et al. petition also contends that the effects of ocean
acidification could have negative impacts on the marine food web within
the California Current ecosystem, including on the NEP population of
white shark. The petition cites a model simulation study which predicts
that by 2050, the oceanic uptake of increased atmospheric
CO2 will lower the pH and the saturation state of aragonite
(a mineral form of calcium carbonate, used by calcifying organisms) in
nearshore waters of the California Current system to levels well below
the natural range for this area (Gruber et al., 2012). The petition
states that these effects of ocean acidification will have negative
impacts on fish species, referencing recent studies showing that high
CO2 and low pH levels impair olfactory responses and homing
ability in clownfish (Munday et al., 2009) and can lead to cardiac
failure in some fish species (Ishimatsu et al., 2004). The petition
readily admits, however, that the severity of effects on specific
species is uncertain. Some fish species may experience metabolic
responses to elevated CO2 levels at the cellular level, but
are able to compensate for those responses at the whole animal level,
making them less sensitive to the effects of ocean acidification
(Portner, 2008). In addition, extrapolating specific effects at the
species levels to the overall ecosystem (e.g., effects on prey
availability and predator-prey interactions for top predators like
white sharks) is highly uncertain. The petition also states that ocean
acidification can potentially affect marine mammals and other marine
life by reducing the sound absorption of seawater and allowing sound to
travel further (Hester et al., 2008). However, the petition does not
explain what the potential effects on marine mammals and other marine
life may be or how any such effects relate to the degradation of white
shark habitat (e.g., the availability or abundance of prey resources).
The available information is not sufficient to determine if ocean
acidification may be threatening the habitat of the NEP population of
white shark such that listing may be warranted.
We conclude that the information in the petitions and in our files
suggests that habitat degradation associated with pollutant discharge
in the Southern California Bight may be impacting the health of the NEP
population of white shark. Human exploitation may have impacted prey
resources (e.g., pinnipeds and fish and invertebrate species) in the
past; however, further analyses are needed to evaluate the recent and
current impacts on prey resources. In addition, the information
provided on the effects of marine debris in the North Pacific Gyre or
ocean acidification is insufficient to evaluate whether these factors
may be threatening the habitat of the NEP population of white shark
such that listing may be warranted.
Overutilization for Commercial, Recreational, Scientific, or
Educational Purposes
Information from both petitions suggests that a primary threat to
the NEP population of white shark is from fisheries. The petitions cite
information on the effects of fisheries on white sharks worldwide and
within the NEP. White sharks are harvested in targeted fisheries and as
bycatch and are highly prized for their teeth, jaws, and fins. White
sharks are primarily caught incidentally in commercial fisheries using
longlines, setlines, gillnets, trawls, fish traps, and other gear
(Compagno, 2001; Fowler et al., 2005; Lowe et al., 2012; Santana-
Morales et al., 2012). The curious nature of white sharks makes them
more vulnerable to incidental capture, and their high value and
negative reputation may contribute to the killing of incidentally
caught individuals rather than being released alive (Fowler et al.,
2005). CITES (2004a) estimated that low to mid hundreds of white sharks
are killed annually as bycatch within each major region of the species'
range. Targeted sport and commercial fisheries for white sharks also
exist worldwide. Targeted sports fisheries may either kill or release
sharks alive, but post-release mortality is unknown. It is estimated
that tens to low hundreds of white sharks are killed in sports
fisheries worldwide each year (CITES, 2004). Targeted commercial
fisheries for white sharks are thought to be uncommon and opportunistic
when
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aggregations are found, but the species' site fidelity and tendency to
aggregate in predictable areas make it vulnerable to over-exploitation
(CITES, 2004). Targeted commercial fisheries worldwide may also kill
tens to low hundreds of white sharks each year (CITES, 2004).
In the NEP Ocean, there is little commercial fishing activity in
the SOFA, providing a potential refuge from incidental capture for
individuals when they occupy this offshore area (Domeier, 2012).
However, the lack of international laws to protect great white sharks
in international waters is a potential threat to the species (Domeier,
2012; discussed further under ``Inadequacy of existing regulatory
mechanisms''). White sharks are most vulnerable to fisheries capture
when occupying nearshore aggregation or nursery habitats, especially
YOY and juvenile stages (Domeier, 2012). Off California, there have
been no directed fisheries for white sharks, but incidental and
targeted catch has occurred (Lowe et al., 2012). An analysis of
fishery-dependent catch records for the Southern California Bight from
1936 to 2009 found that the majority of the reported white shark
captures (where size was indicated) were of YOY sharks (60 percent),
followed by juveniles (32 percent) and subadults/adults (8 percent);
however, the proportion of YOY sharks in the reported catch increased
to 77 percent after the nearshore gillnet ban was implemented in 1994
(Lowe et al., 2012). Commercial entangling nets (81 percent) and
recreational hook-and-line fishing (8 percent) accounted for the
majority of the reported white shark captures (Lowe et al., 2012). The
number of reported white shark captures in commercial entangling nets
has been 20 or less from 1985 through 2009, except in 1985 when 25
captures were reported (Lowe et al., 2012). The analysis suggests that
the effects of incidental capture in gillnet fisheries off California
have decreased compared to historical effects. As gillnet fishing
effort decreased from the mid-1980s to mid-1990s, so did reports of
white shark captures (Lowe et al., 2012). However, although gillnet
fishing effort remained stable or decreased from the mid-1990s through
2009, reports of white shark captures increased from 2005 through 2009
(Lowe et al., 2012). Increases in the number of reported captures in
the gillnet fisheries since 2005, despite stable or decreased effort,
may be the result of increased reporting of captures and/or an increase
in the abundance of white sharks due to the nearshore gillnet ban and
changes in offshore gillnet regulations (Lowe et al., 2012). Also, data
from the Monterey Bay Aquarium's Juvenile White Shark Tagging Program
indicate that YOY and juvenile white sharks have relatively high post-
release survival after being caught in gillnet gear (Lowe et al.,
2012).
Incidental catch of white sharks also continues to occur off Baja
California. Incidental catch of 111 great white sharks was reported
from 1999 through 2010, consisting of YOY (79.8 percent) and juvenile
(20.2 percent) sharks (Santana-Morales et al., 2012). Incidental catch
primarily occurred in bottom gillnet gear (74.7 percent), but also in
drift gillnet (18 percent) and artisanal seine net (4.5 percent) gear
(Santana-Morales et al., 2012).
The petitions assert that the continued incidental catch of white
sharks poses a threat to the species, because the removal of just a few
individuals could have a substantive effect on the local population
(Pyle et al., 1996; Chapple, 2011). The petitions also highlight the
high value of white shark teeth, jaws, and fins as trophies, curios,
and food, stating that this provides a strong monetary incentive to
capture and keep white sharks (Clarke, 2004; Shivji et al., 2005;
Clarke et al., 2006).
We conclude that the petitions and information in our files present
evidence that fisheries impacts continue to affect white shark
populations worldwide and in the NEP, primarily due to incidental
capture in fisheries and the potential for the high value of great
white shark teeth, jaws, and fins to promote keeping incidentally
caught individuals rather than releasing them back into the water. This
information suggests that fisheries impacts may be affecting the
continued existence of the NEP population of white shark. To further
evaluate these effects, more information is needed on fisheries impacts
specifically within the range of the NEP population, particularly on
the capture of white sharks in fisheries in offshore waters and the
lethal and sublethal effects of catch and release.
Disease or Predation
The WildEarth Guardians petition asserts that the addition of
mercury, organochlorine contaminants, and other pollutants to the ocean
and the effects of these pollutants on the NEP population of white
sharks may be categorized as disease. The petition does not provide any
additional information to support that disease is a factor affecting
the NEP population's continued existence such that listing may be
warranted. Thus, the available information is insufficient to evaluate
if disease may be affecting the continued existence of the NEP
population of white shark. The petition more appropriately discusses
pollutants and their effects on the NEP population under the habitat
degradation and ``other natural or manmade'' factors.
Inadequacy of Existing Regulatory Mechanisms
The petitions assert that the inadequacy of existing Federal,
state, or international regulatory mechanisms require that the NEP
population of white shark be listed under the ESA. The petitions
contend that although Federal, state, and international regulations
exist to protect white sharks from targeted capture in some areas,
these regulations are insufficient because white sharks in the NEP
population are still vulnerable to incidental capture throughout its
range, and to exploitation when in international waters. In addition,
the WildEarth Guardians petition states that existing regulations do
not protect the NEP population's habitat and health from threats such
as habitat degradation, pollution, and overfishing of prey resources.
Within the United States, Federal and state regulations to protect
white sharks vary. Currently, the retention of white sharks in U.S.
Federal waters in the Pacific Ocean is prohibited under the Highly
Migratory Species Fishery Management Plan. In California, targeted
capture of white sharks is prohibited, but incidentally caught white
sharks may be retained under a permit from the California Department of
Fish and Game for scientific or educational purposes (14 CCR Sec.
28.06). In Oregon, all white sharks must be released immediately if
caught (ODFW, 2012). Washington and Hawaii do not have specific
fisheries regulations for white shark. However, both Hawaii and
California passed bans making it unlawful to possess, sell, offer for
sale, trade, or distribute shark fins, which may provide some
protection for white sharks. The petitions argue that despite these
protections, the continued incidental capture and mortality of even
small numbers of white sharks in U.S. waters, particularly off
California, can have a large impact on the local population, citing a
study off the Farallon Islands in which the removal of four white
sharks from the area in 1982 resulted in significantly fewer sightings
of shark attacks on pinnipeds than expected in 1983 to 1985 (Pyle et
al., 1996). The petitions also suggest that illegal fishing may be a
problem in the United States, citing cases of illegal
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fishing and sale of white shark teeth, jaws, and fins in 2003 (CITES,
2004).
Outside of the United States, protections for white sharks also
vary. In Mexico, catch and retention of white sharks and the landing of
shark fins without carcasses has been banned since 2006 (Lack and Sant,
2011), although incidental capture continues to occur (Galv[aacute]n-
Maga[ntilde]a et al., 2010; Santana-Morales et al., 2012). In Canada,
there are no specific regulations to protect white sharks, although a
ban on shark finning may provide some protection (DFO, 2007). In
international waters, white sharks are protected under CITES (Appendix
II) and other international agreements, including the Convention on
Migratory Species (Appendix I and II) and the United Nations Convention
on the Law of the Sea. However, the petitions contend that these
protections are not sufficient, given continued trade in white shark
products due to poaching and variable enforcement of regulations
(CITES, 2004; Clarke, 2004; Shivji et al., 2005; Clarke et al., 2006;
Galv[aacute]n-Maga[ntilde]a et al., 2010; Jorgensen et al., 2010;
Viegas, 2011).
Based on the information in the petition and in our files as
discussed above, we conclude that existing regulatory mechanisms may be
inadequate to address threats to the NEP population of white shark. To
further evaluate the adequacy of existing regulatory mechanisms, more
information is needed regarding the level of illegal fishing and
poaching in U.S. and international waters.
Other Natural or Manmade Factors
The two petitions assert that other natural or manmade factors may
be affecting the survival and recovery of the NEP population of white
shark, including contaminant loads, negative press, life history
factors, small population size, and the synergistic effects of all of
the threats facing the population. Both petitions cite a study
conducted in the Southern California Bight revealing mercury and
organochlorines (e.g., DDT, PCBs, and chlordanes) in the tissues of
juvenile white sharks at levels that may result in physiological
impairment (Mull et al., 2012). Young white sharks are likely
bioaccumulating these contaminants (likely from historical discharges
in the Southern California Bight) when feeding on prey resources in the
area (Blasius and Goodmanlowe, 2008; Mull et al., 2012). The WildEarth
Guardian petition also cites negative media attention as a threat to
white sharks, especially when shark attacks on humans occur, because
this generates general paranoia and encourages targeting of the species
for sport or trophy hunting (IUCN, 2009).
The WildEarth Guardians petition asserts that natural factors,
including the species' life history characteristics and small
population size, also increase the extinction risk of the NEP
population of white shark, particularly when considered in combination
with other threats to the species. The petition states that the
species' life history characteristics (e.g., slow growth, late
maturation, long-life, long generation time, small litter size, and low
reproductive capacity) make it susceptible to extinction when faced
with population declines and continuing threats (Withgott and Brennan,
2007). The petition also contends that the small estimated population
size (e.g., approximately 340 subadults and adults in the NEP
population; Chapple et al., 2011; Sosa-Nishizaki et al., 2012) makes
the population highly susceptible to extinction due to a stochastic
event (Brook et al., 2008). We note, however, that this estimate of
abundance is based on studies of individuals surveyed in aggregation
sites off central California and Guadalupe Island, and do not include
YOY and juveniles. Also, without information on the historical
abundance of the NEP population, it is difficult to assess what this
estimated population size means for the persistence of the population.
The low estimated abundance of the population may be the result of
anthropogenic pressures on the population or a naturally low carrying
capacity (the NEP population is thought to have been established by a
limited number of founders from the ANZ population; Jorgensen et al.,
2010) (Chapple et al., 2011). Catch ratios of white sharks to all shark
species off the U.S. west coast from 1965 (1:67) to 1983 (1:210)
suggest a potential decline in abundance (Casey and Pratt, 1985, cited
in Fowler et al., 2005). However, recent increases in the incidental
capture of white sharks in gillnet fisheries off California, despite
stable or decreasing fishing effort, suggest that the population may be
increasing (Lowe et al., 2012). In addition, an increased frequency of
observed white shark attacks on pinnipeds off the South Farallon
Islands over time indicates an increase in the shark population at the
islands (Pyle et al., 1996; Pyle et al., 2003). Thus, it is difficult
at this time to determine population trends and to evaluate how the
estimated size of the NEP population relates to the population's
extinction risk.
Overall, the petition and information in our files suggest that
effects from bioaccumulation of contaminants and negative media
attention, coupled with the life history characteristics of white
sharks, may be affecting the survival and recovery of the NEP
population. More specific information is needed, however, to assess
population trends and to evaluate the population's estimated abundance
in terms of the potential effects on the population's survival and
recovery.
Summary of Section 4(a)(1) Factors
We conclude that the petition presents substantial scientific or
commercial information indicating that multiple section 4(a)(1)
factors, as discussed above, may be causing or contributing to an
increased risk of extinction for the NEP population of white shark.
Petition Finding
After reviewing the information contained in both petitions, as
well as information readily available in our files, we conclude the
petitions present substantial scientific information indicating the
petitioned action of listing the NEP population of white shark as a
threatened or endangered DPS may be warranted. Therefore, in accordance
with section 4(b)(3)(A) of the ESA and NMFS' implementing regulations
(50 CFR 424.14(b)(3)), we will commence a status review of the species.
During the status review, we will determine whether the population
identified by the petitioners meets the DPS policy's criteria, and if
so, whether the population is in danger of extinction (endangered) or
likely to become so within the foreseeable future (threatened)
throughout all or a significant portion of its range. We now initiate
this review, and thus, the northeastern Pacific Ocean population of
white shark is considered to be a candidate species (50 CFR 424.15(b)).
Within 12 months of the receipt of the WildEarth Guardians petition
(June 25, 2013), we will make a finding as to whether listing the
species as endangered or threatened is warranted as required by section
4(b)(3)(B) of the ESA. If listing the species is warranted, we will
publish a proposed rule and solicit public comments before developing
and publishing a final rule.
Information Solicited
To ensure that the status review is based on the best available
scientific and commercial data, we are soliciting information relevant
to whether the NEP Ocean population of white sharks is a DPS and
whether it is threatened or endangered. Specifically, we are soliciting
published and unpublished
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information in the following areas: (1) Population structure
information in the Pacific Ocean, such as genetics data; particularly
any unpublished information; (2) migratory and behavior patterns in the
NEP Ocean, particularly any unpublished information; (3) life history
and ecology, particularly any unpublished information; (4) historical
and current distribution and abundance of this species throughout the
NEP Ocean; (5) historical and current population trends in the NEP
Ocean; (6) historical and current data on commercial and recreational
fisheries directed at white sharks in the NEP Ocean, including Mexican
waters; (7) historical and current data on white shark bycatch and
retention in commercial and recreational fisheries in the NEP Ocean,
including Mexican waters; (8) data on the trade of white shark
products, including fins, jaws, and teeth in the NEP Ocean, including
Mexico; (9) data or other information on encounter rates with white
sharks through ecotourism operations and sightings data, and long-term
records of white shark attacks, wounds or scaring of marine mammals;
(10) adverse impacts related to coastal habitat degradation and the
health of white sharks, including, but not limited to, impacts related
to discharge of pollutants, marine debris, or ocean acidification; (11)
any current or planned activities that may adversely impact the
species; (12) ongoing or planned efforts to protect and restore the
species and their habitats; and (12) management, regulatory, and
enforcement information.
We also request information on critical habitat for the NEP Ocean
population of white sharks. Specifically, we request information on the
physical and biological habitat features that are essential to the
conservation of the species and identification of habitat areas that
include these essential physical and biological features. Essential
features include, but are not limited to: (1) Space for individual and
population growth and for normal behavior; (2) food, water, air, light,
minerals, or other nutritional or physiological requirements; (3) cover
or shelter; (4) sites for reproduction and development of offspring;
and (5) habitats that are protected from disturbance or are
representative of the historical, geographical, and ecological
distributions of the species (50 CFR 424.12). For habitat areas
potentially qualifying as critical habitat, we request information
describing: (1) The activities that affect the habitat areas or could
be affected by the designation; and (2) the economic impacts, impacts
to national security, or other relevant impacts of additional
requirements of management measures likely to result from the
designation.
We request that all information be accompanied by: (1) Supporting
documentation such as maps, raw data with associated documentation,
bibliographic references, or reprints of pertinent publications; and
(2) the submitter's name, mailing address, email address, and any
association, institution, or business that the person represents.
References Cited
A complete list of references is available upon request from the
NMFS Southwest Regional Office (see ADDRESSES).
Authority
The authority for this action is the Endangered Species Act of
1973, as amended (16 U.S.C. 1531 et seq.).
Dated: September 25, 2012.
Alan D. Risenhoover,
Director, Office of Sustainable Fisheries, performing the functions and
duties of the Deputy Assistant Administrator for Regulatory Programs,
National Marine Fisheries Service.
[FR Doc. 2012-23963 Filed 9-27-12; 8:45 am]
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