Endangered and Threatened Wildlife and Plants; 12-Month Finding on a Petition To List the Ashy Storm-Petrel as Threatened or Endangered, 41832-41860 [E9-19700]
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Federal Register / Vol. 74, No. 159 / Wednesday, August 19, 2009 / Proposed Rules
List of Subjects in 47 CFR Part 73
Radio, Radio broadcasting.
For the reasons discussed in the
preamble, the Federal Communications
Commission proposes to amend 47 CFR
Part 73 as follows:
PART 73—RADIO BROADCAST
SERVICES
1. The authority citation for part 73
continues to read as follows:
Authority: 47 U.S.C. 154, 303, 334, 336.
§ 73.202
[Amended]
2. Section 73.202(b), the Table of FM
Allotments under Oregon, is amended
by adding Maupin, Channel 244C2.
Andrew J. Rhodes,
Senior Counsel, Allocations, Audio Division,
Media Bureau, Federal Communications
Commission.
[FR Doc. E9–19872 Filed 8–18–09; 8:45 am]
BILLING CODE 6712–01–P
FEDERAL COMMUNICATIONS
COMMISSION
47 CFR Part 73
[DA 09–1795; MB Docket No. 09–146; RM–
11553]
Television Broadcasting Services;
Chicago, IL
CPrice-Sewell on DSK1DXX6B1PROD with PROPOSALS
AGENCY: Federal Communications
Commission.
ACTION: Proposed rule.
SUMMARY: The Commission has before it
a petition for rulemaking filed by WLS
Television, Inc. (‘‘WLS’’), the licensee of
station WLS–TV, DTV channel 7,
Chicago, Illinois. WLS–TV requests the
substitution of transition DTV channel
44 for its post-transition DTV channel 7
at Chicago.
DATES: Comments must be filed on or
before September 3, 2009, and reply
comments on or before September 14,
2009.
ADDRESSES: Federal Communications
Commission, Office of the Secretary,
445 12th Street, SW., Washington, DC
20554. In addition to filing comments
with the FCC, interested parties should
serve counsel for petitioner as follows:
Tom W. Davidson, Esq., Akin Gump
Strauss Hauer & Feld, LLP, 1333 New
Hampshire Ave., NW., Washington, DC
20026.
FOR FURTHER INFORMATION CONTACT:
Adrienne Y. Denysyk,
adrienne.denysyk@fcc.gov, Media
Bureau, (202) 418–1600.
SUPPLEMENTARY INFORMATION: This is a
synopsis of the Commission’s Notice of
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Proposed Rule Making, MB Docket No.
09–146, adopted August 11, 2009, and
released August 12, 2009. The full text
of this document is available for public
inspection and copying during normal
business hours in the FCC’s Reference
Information Center at Portals II, CY–
A257, 445 12th Street, SW.,
Washington, DC, 20554. This document
will also be available via ECFS (https://
www.fcc.gov/cgb/ecfs/). (Documents
will be available electronically in ASCII,
Word 97, and/or Adobe Acrobat.) This
document may be purchased from the
Commission’s duplicating contractor,
Best Copy and Printing, Inc., 445 12th
Street, SW., Room CY–B402,
Washington, DC 20554, telephone 1–
800–478–3160 or via e-mail https://
www.BCPIWEB.com. To request this
document in accessible formats
(computer diskettes, large print, audio
recording, and Braille), send an e-mail
to fcc504@fcc.gov or call the
Commission’s Consumer and
Governmental Affairs Bureau at (202)
418–0530 (voice), (202) 418–0432
(TTY). This document does not contain
proposed information collection
requirements subject to the Paperwork
Reduction Act of 1995, Public Law 104–
13. In addition, therefore, it does not
contain any proposed information
collection burden ‘‘for small business
concerns with fewer than 25
employees,’’ pursuant to the Small
Business Paperwork Relief Act of 2002,
Public Law 107–198, see 44 U.S.C.
3506(c)(4).
Provisions of the Regulatory
Flexibility Act of 1980 do not apply to
this proceeding. Members of the public
should note that from the time a Notice
of Proposed Rule Making is issued until
the matter is no longer subject to
Commission consideration or court
review, all ex parte contacts are
prohibited in Commission proceedings,
such as this one, which involve channel
allotments. See 47 CFR 1.1204(b) for
rules governing permissible ex parte
contacts.
For information regarding proper
filing procedures for comments, see 47
CFR 1.415 and 1.420.
List of Subjects in 47 CFR Part 73
Television, Television broadcasting.
For the reasons discussed in the
preamble, the Federal Communications
Commission proposes to amend 47 CFR
part 73 as follows:
PART 73—RADIO BROADCAST
SERVICES
1. The authority citation for part 73
continues to read as follows:
Authority: 47 U.S.C. 154, 303, 334, 336.
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§ 73.622(i)
[Amended]
2. Section 73.622(i), the PostTransition Table of DTV Allotments
under Illinois, is amended by adding
DTV channel 44 and removing DTV
channel 7 at Chicago.
Federal Communications Commission.
Clay C. Pendarvis,
Associate Chief, Video Division, Media
Bureau.
[FR Doc. E9–19875 Filed 8–18–09; 8:45 am]
BILLING CODE 6712–01–P
DEPARTMENT OF THE INTERIOR
Fish and Wildlife Service
50 CFR Part 17
[FWS-R8-ES-2008-0049;1111 FY08 MO-B2]
Endangered and Threatened Wildlife
and Plants; 12-Month Finding on a
Petition To List the Ashy Storm-Petrel
as Threatened or Endangered
AGENCY: Fish and Wildlife Service,
Interior.
ACTION: Notice of 12–month petition
finding.
SUMMARY: We, the U.S. Fish and
Wildlife Service (Service), announce a
12–month finding on a petition to list
the ashy storm-petrel (Oceanodroma
homochroa) as threatened or
endangered, under the Endangered
Species Act of 1973, as amended (Act).
After a thorough review of all available
scientific and commercial information,
we find that listing the ashy stormpetrel is not warranted. We ask the
public to continue to submit to us any
new information concerning the status
of, and threats to, this species. This
information will help us to monitor and
encourage the conservation of this
species.
DATES: The finding announced in the
document was made on August 19,
2009.
ADDRESSES: This finding is available on
the Internet at https://
www.regulations.gov and https://
www.fws.gov/arcata/. Supporting
documentation we used in preparing
this finding is available for public
inspection, by appointment, during
normal business hours at the U.S. Fish
and Wildlife Service, Arcata Fish and
Wildlife Office, 1655 Heindon Road,
Arcata, CA 95521; telephone 707-8227201; facsimile 707-822-8411. Please
submit any new information, materials,
comments, or questions concerning this
finding to the above address.
FOR FURTHER INFORMATION CONTACT:
Randy Brown, (Acting) Field
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Supervisor, U.S. Fish and Wildlife
Service, Arcata Fish and Wildlife Office
(see ADDRESSES section). If you use a
telecommunications device for the deaf
(TDD), call the Federal Information
Relay Service (FIRS) at 1-800-877-8339.
SUPPLEMENTARY INFORMATION:
CPrice-Sewell on DSK1DXX6B1PROD with PROPOSALS
Background
Section 4(b)(3)(B) of the Act (16
U.S.C. 1531 et seq.) requires that, for
any petition to revise the Lists of
Endangered and Threatened Wildlife
and Plants that contains substantial
scientific and commercial information
that listing may be warranted, we make
a finding within 12 months of the date
of our receipt of the petition on whether
the petitioned action is: (a) Not
warranted, (b) warranted, or (c)
warranted, but the immediate proposal
of a regulation implementing the
petitioned action is precluded by other
pending proposals to determine whether
any species is threatened or endangered,
and expeditious progress is being made
to add or remove qualified species from
the Lists of Endangered and Threatened
Wildlife and Plants. Such 12–month
findings are to be published promptly in
the Federal Register. Section 4(b)(3)(C)
of the Act requires that we treat a
petition for which the requested action
is found to be warranted but precluded
as though resubmitted on the date of
such finding, and we must make a
subsequent finding within 12 months.
Previous Federal Actions
On October 16, 2007, we received a
petition, dated October 15, 2007, from
the Center for Biological Diversity (CBD
or petitioner), requesting that we list the
ashy storm-petrel as a threatened or
endangered species throughout its range
and that we concurrently designate
critical habitat (CBD 2007, pp. 1-51). In
response to the petition, we sent a letter
to the petitioner dated January 11, 2008,
stating that we had secured funding and
that we anticipated making an initial
finding as to whether the petition
contained substantial information
indicating listing the ashy storm-petrel
may be warranted in Fiscal Year 2008.
We also concluded in our January 11,
2008, letter that emergency listing of the
ashy storm-petrel was not warranted.
On May 15, 2008, we published a 90–
day petition finding (73 FR 28080) in
which we concluded that the petition
provided substantial information
indicating that listing of the ashy stormpetrel may be warranted, and we
initiated a status review. This notice
constitutes the 12–month finding on the
petition, dated October 15, 2007, to list
the ashy storm-petrel as threatened or
endangered.
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Species Description
The ashy storm-petrel is a seabird
species belonging to the order
Procellariiformes, family Hydrobatidae.
The ashy storm-petrel is one of five
storm-petrel species (including forktailed (Oceanodroma furcata), Leach’s
(O. leucorhoa), black (O. melania), and
least (O. microsoma) storm-petrels) that
nest on islands along the west coast of
North America (Harrison 1983, pp. 272278). The ashy storm-petrel is a smokegray, medium-sized bird with long
slender wings, a long forked tail, and
webbed feet (Ainley 1995, p. 2).
Ashy storm-petrels have been
confirmed to breed at 26 locations (on
islands and offshore rocks) from
Mendocino County, California, south to
Todos Santos Islands, west of Ensenada,
Baja California, Mexico (Carter et al.
1992, pp. 77-81; Ainley 1995, p. 2;
Carter et al. 2006, p. 6; Carter et al.
2008a, p. 118). Greater than 95 percent
of the species breeds in two population
centers at the Farallon Islands and in
the California Channel Islands (Sowls et
al. 1980, p. 24; Ainley et al. 1990, p.
135; Carter et al. 1992, p. 86). Anacapa,
San Miguel, Santa Cruz, Santa Rosa, San
Clemente, San Nicholas, Santa Barbara,
and Santa Catalina islands comprise the
Channel Islands.
Ashy storm-petrels occur at their
breeding colonies nearly year-round and
occur in greater numbers from February
through October (Ainley 1995, p. 5).
Like other procellariids, ashy stormpetrels are highly philopatric; that is,
birds usually return in consecutive
years to the same breeding site or colony
from which they were raised as chicks
(James-Veitch 1970, p. 81; Warham
1990, p. 12). Ashy storm-petrels do not
excavate burrows; rather, they nest in
crevices of talus slopes, rock walls, sea
caves, cliffs, and driftwood (JamesVeitch 1970, pp. 87-88; Ainley et al.
1990, p. 147; McIver 2002, p. 1). The
breeding season is protracted, and
breeding activities (courtship, egglaying, chick-rearing) at nesting
locations occur from February through
January of the following year (JamesVeitch 1970, p. 71, Ainley et al. 1974,
p. 301). During the pre-egg period, adult
ashy storm-petrels begin to visit nesting
sites in February (Ainley et al. 1974, p.
301; Ainley 1995, p. 5). Throughout the
fledging period, the number of visiting
adults declines (Ainley et al. 1974, p.
301). At Southeast Farallon Island,
Ainley et al. (1974, p. 301) reported that
immature (non-breeding) ashy stormpetrels visited the island from April
through early July. The egg-laying
period extends from late April to
October, peaking in June and July
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(James-Veitch 1970, p. 243; Ainley et al.
1990, p. 148; McIver 2002, p. 17). Clutch
size is one egg per year, and parents
alternate incubation bouts during a 44–
day incubation period (James-Veitch
1970, p. 244; Ainley 1995, p. 6). Less
than about 4 percent of all eggs laid are
replacement (or re-lay) eggs, laid after
the failure of a first egg (Ainley et al.
1990, p. 148; McIver 2002, p. 18).
Hatchlings are ‘‘semi-precocial’’ (JamesVeitch 1970, p. 128). The term semiprecocial describes young that have
characteristics of precocial young at
hatching (open eyes, downy, capacity to
leave the nest), but that remain at the
nest and are cared for by parents until
close to adult size (Sibley 2001, p. 573).
Once hatched, the nestling is brooded
for about 5 days, after which it remains
alone in the nest site for an additional
75 to 85 days (James-Veitch 1970, pp.
141, 212; Ainley et al. 1990, p. 152). It
is fed irregularly (1 to 3 nights on
average) during brief, nocturnal visits by
its parents from feeding areas at sea
(James-Veitch 1970, pp. 180-208).
Fledging occurs at night, from late
August to January, and once they leave
the nest, fledglings are independent of
their parents (Ainley et al. 1974, p. 303;
McIver 2002, p. 36). Peak fledging
occurs in early to mid-October (McIver
2002, p. 18).
The nocturnal activity (return to and
departure from nest) and crevice nesting
of the ashy storm-petrel are believed to
be adaptations to avoid predation by
diurnal predators, such as western gulls
(Larus occidentalis), peregrine falcons
(Falco peregrinus), and common ravens
(Corvus corax) (Ainley 1995, p. 5;
McIver and Carter 2006, p. 3). Ashy
storm-petrels are susceptible to
predation at night by burrowing owls
(Athene cunicularia) and barn owls
(Tyto alba) (Ainley 1995, p. 5; McIver
2002, p. 30). Nesting in crevices and
burrows on remote headlands, offshore
rocks, and islands generally reduces
predation of storm-petrels by
mammalian predators (Warham 1990, p.
13). Known mammalian predators of
ashy storm-petrels and their eggs
include house mice (Mus musculus),
deer mice (Peromyscus maniculatus),
and island spotted skunks (Spilogale
gracilis amphiala) (Ainley et al. 1990, p.
146; McIver 2002, pp. 40-41; McIver and
Carter 2006, p. 3).
Obtaining direct population counts of
ashy storm-petrels is difficult because
the species often nests in deep,
inaccessible crevices (Carter et al. 1992,
p. 77; Sydeman et al. 1998a, p. 438).
Techniques for estimating population
size at breeding locations have included
counting crevices and applying
correction factors to account for burrow
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occupancy, mark and recapture using
mist nests, and direct observation of
nest sites. Estimates of breeding ashy
storm-petrels for California have ranged
from 5,187 (Sowls et al. 1980, p. 25) to
7,209 (Carter et al. 1992, p. I-87).
Additional colony sites and larger ashy
storm-petrel numbers have been found
at several locations in the Channel
Islands and along the mainland coast of
California (Carter et al. 2008a, p. 119).
Table 1 provides various estimates of
numbers of breeding ashy storm-petrels
at 26 locations in California and Baja
California Norte, Mexico.
TABLE 1. ESTIMATES OF NUMBERS OF BREEDING ASHY STORM-PETRELS AT 26 LOCATIONS IN CALIFORNIA (UNITED
STATES) AND BAJA CALIFORNIA NORTE (MEXICO).
Ownership or
Managementa
Location
Source for
Breeding Birds
Estimatesb
Estimated No.
Breeding Birds
Bird Rock near Greenwood, Mendocino County
BLM
10
1,2,3
2
Caspar, near Point Cabrillo, Mendocino County
BLM
10
1,2,3
3
Bird Rock, Marin County
NPS
10
4
4
Stormy Stack, Marin County
NPS
10
4
5a
Southeast Farallon Island
FWS
4,000
5
5b
Southeast Farallon Island
FWS
3,402
6
5c
Southeast Farallon Island
FWS
1,990
6
6
Castle/Hurricane Colony Complex, Monterey County
BLM
60
7
7
Castle Rock, Santa Barbara County
USN/NPS
200
8
8
Prince Island
USN/NPS
1,154
1
9
Shipwreck Cave, Santa Cruz Island
TNC/NPS
20
9
10
Dry Sandy Beach Cave, Santa Cruz Island
TNC/NPS
80
10,11,12,13
11
Del Mar Rock, Santa Cruz Island
NPS
10
1
12
Cave of the Bird’s Eggs, Santa Cruz Island
TNC/NPS
52
10,11,12,13
13
Diablo Rocks, Santa Cruz Island
NPS
20
8
14
Orizaba (‘‘Sppit’’) Rock, Santa Cruz Island
NPS
40
10,11,12,13
15
Bat Cave, Santa Cruz Island
NPS
48
10,11,12,13
16
Cavern Point Cove Caves, Santa Cruz Island
NPS
0
10,11,12,13
17
Scorpion Rocks, Santa Cruz Island
NPS
140
1
18
Willows Anchorage Rocks, Santa Cruz Island
NPS
111
1
19
Gull Island
NPS
2
8
20
Santa Barbara Island
NPS
874
1
21
Sutil Island
NPS
586
1
22
Shag Rock
NPS
10
13
23
Ship Rock, Santa Catalina Island
BLM
2
14
24
Seal Cove Area, San Clemente Island
BLM
10
15
25
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1
Islas Los Coronados, Mexico
MX
100
16
26
Islas Todos Santos, Mexico
MX
10
17
Total, if using line 5a
7,569
Total, if using line 5b
6,971
Total, if using line 5c
5,559
aEntity
listed once if same for both ownership and management, as follows: Bureau of Land Management (BLM); Mexican Government (MX);
National Park Service (NPS); The Nature Conservancy (TNC); U.S. Fish and Wildlife Service (FWS); and U.S. Navy (USN).
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bSources are as follows: 1-Carter et al. 1992; 2-Carter et al. 2008a; 3-Carter et al. unpublished notes; 4-Whitworth et al. 2002; 5-Ainley and
Lewis 1974; 6-Sydeman et al. 1998a; 7-McChesney et al. 2000; 8-Hunt et al. 1979; 9-H. Carter, unpublished data; 10-McIver 2002; 11-McIver
and Carter 2006; 12-Carter et al. 2007; 13-McIver et al. 2008; 14-FWS estimate, based on Carter et al. 2008a; 15-H. Carter and D. Whitworth,
unpublished data; 16-Carter et al. 2006a; and 17-Carter et al 2006b.
Four thousand to six thousand ashy
storm-petrels are usually observed in
the fall in Monterey Bay, approximately
3 to 10 miles (mi) (5 to 16 kilometers
(km)) offshore from the town of Moss
Landing, California. As many as 10,000
ashy storm-petrels were estimated to be
present in Monterey Bay in October
1977 and in September 2008 (Roberson
1985, p. 42; Shearwater Journeys 2008).
However, both of these estimates were
from non-standardized visual estimates.
Spear and Ainley (2007, p. 27)
examined the seasonal at-sea
distributions and abundance of stormpetrel species (including ashy stormpetrels) with generalized additive
models, and estimated 4,207 and 7,287
birds during autumn and spring,
respectively (95 percent confidence
interval: 2,700 to 6,400 in autumn and
4,500 to 9,070 in spring) off of Sonoma
to Monterey counties. Spear and Ainley
(2007, p. 7) suggested that higher
numbers of ashy storm-petrels may
occur at Southeast Farallon Island, and
other of the Farallon Islands, than have
previously been reported. The total
population of ashy storm-petrels
(including breeders and non-breeders)
has been estimated to be approximately
10,000 birds (Sowls et al. 1980, p. 24;
Ainley 1995, p.1). Based on estimates at
breeding locations and at-sea
observations in Monterey Bay and off
Sonoma to Monterey counties, we
consider 7,000 to 10,000 birds to be a
reasonable estimate of the total
population size of ashy storm-petrels.
However, based on other visual
estimates mentioned above, the total
population could be as high as 13,000
birds.
More ashy storm-petrels breed at
Southeast Farallon Island than at any
other single location (Sowls et al. 1980,
p. 24; Carter et al. 1992, p. I-78).
Assessing population size and trends
has been done through capture-
recapture techniques using audio
playback and mist nets (see Ainley and
Lewis 1974, p. 435; Sydeman et al.
1998a, p. 438). Ainley and Lewis (1974,
pp. 432-435) estimated 4,000 breeding
ashy storm-petrels at Southeast Farallon
Island in years 1971 to 1972, from birds
captured and recaptured in mist nets at
night. Sydeman et al. (1998a, p. 438442) re-analyzed data from Southeast
Farallon Island for years 1971 and 1972
(Ainley and Lewis 1974) and included
data from year 1992 to estimate 6,461
total ashy storm-petrels and 3,402
breeding ashy storm-petrels in 1971 to
1972, and 4,284 total ashy storm-petrels
and 1,990 breeding ashy storm-petrels
in 1992. Based on comparison of these
data sets, Sydeman et al. (1998a, p. 442)
suggested declines of 34 percent and 42
percent in the total population and
breeding population of ashy stormpetrels, respectively, at Southeast
Farallon Island. Sydeman et al. (1998a,
pp. 445-446) reported that this decline
occurred in prime storm-petrel nesting
habitat, and suggested that this decline
in population size at Southeast Farallon
Island was due to, in part, an increase
in the predation rate on ashy stormpetrel adults and sub-adults by western
gulls and burrowing owls. We interpret
these results cautiously because they are
based on two data points: one from 1972
and one 20 years later from 1992.
Sydeman et al. (1998b, pp. 1-74)
conducted a population viability
assessment of ashy storm-petrels at
Southeast Farallon Island, quantitatively
examining the effects of predation on
population decrease of ashy stormpetrels. Sydeman et al. (1998b, pp. 1-2)
estimated a 2.87 percent decline in the
population of ashy storm-petrels from
1972 to 1992 and hypothesized that
removal of western gull predation
would produce a stable population.
They also stated, given current
population parameters and predation
rates, the population of ashy stormpetrels faces a high probability of quasiextinction within 50 years (Sydeman et
al. 1998b, p. 2). Since 1992, capturerecapture of ashy storm-petrels at
Southeast Farallon Island has continued
and techniques have been further
standardized (McChesney 2008, p. 4).
Using data from 1999 to 2007, Warzybok
and Bradley (2007, p. 17) describe
analysis of capture-recapture data that
shows increasing capture rates and
increasing survival of ashy stormpetrels. Specifically, they report the
mean standardized capture rate (number
of birds caught per hour of effort)
increased from approximately 13 birds
per hour to 38 birds per hour between
1999 and 2005 but declined slightly in
2006. The mean capture rate for 2007
was 39 birds per hour (Warzybok and
Bradley 2007, p. 17). The authors also
note that there were a greater number of
occupied nesting sites than in previous
years. Although there are caveats
associated with Warzybok and Bradley’s
(2007) analysis (See Factor C: Disease
and Predation section below), their
report represents the best available
information to date and suggests an
increasing population of ashy stormpetrels.
Research on reproductive success (or
productivity, defined as number of
fledged chicks per adult pair) of the
ashy storm-petrel has been conducted
only at Southeast Farallon Island
(James-Veitch 1970, pp. 1-366; Ainley et
al. 1990, pp. 128-162; Sydeman et al.
1998a, pp. 1-74; PRBO Conservation
Science,) and Santa Cruz Island (McIver
2002, pp. 1-70; McIver and Carter 2006,
pp. 1-6; Carter et al. 2007, pp. 1-32;
McIver et al. 2008, pp. 1-23; McIver et
al. 2009, pp. 1-30; McIver et al., in
preparation, pp. 1-23). Reported
productivity values are presented in
Table 2.
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TABLE 2. AVERAGE VALUES FOR PRODUCTIVITY (FLEDGED CHICKS PER ADULT PAIR) OF ASHY STORM-PETRELS AT SOUTHEAST FARALLON ISLAND AND SANTA CRUZ ISLAND, CALIFORNIA, FOR SEVERAL STUDIES DURING 1964-1966 AND
1971-2008. SAMPLE SIZES ARE SHOWN IN PARENTHESES.
Location
Productivity
Southeast Farallon Island
0.42a(n
Southeast Farallon Island
Source
1964-1966
James-Veitch (1970)
0.69(n = 356)
1972-1983b
Ainley and Boekelheide (1990)
Southeast Farallon Island
0.74d(n = 540)
1971-1992b
Sydeman et al. (1998b)
Southeast Farallon Island
0.54c(n = 283)
1996-2007e
PRBO Conservation Science unpublished data; Warzybok
and Bradley (2007)
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= 184)
Years
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TABLE 2. AVERAGE VALUES FOR PRODUCTIVITY (FLEDGED CHICKS PER ADULT PAIR) OF ASHY STORM-PETRELS AT SOUTHEAST FARALLON ISLAND AND SANTA CRUZ ISLAND, CALIFORNIA, FOR SEVERAL STUDIES DURING 1964-1966 AND
1971-2008. SAMPLE SIZES ARE SHOWN IN PARENTHESES.—Continued
Location
Productivity
Years
Source
Santa Cruz Island
0.55(n = 477)
1995-1998
McIver et al. in preparation, Table 4
Santa Cruz Island
0.65(n = 293)
2005-2008
McIver et al. in preparation, Table 4; McIver et al. (2009)
aResearcher
disturbance (daily nest checks) negatively affected productivity.
year 1977, when researcher disturbance negatively affected productivity.
cSample sizes not provided for year 1996-2005, so annual sample size during this time period. assumed at 22 nests, based on average sample size in Sydeman et al. (1998b).
dBased on two data points.
eBased on yearly date.
bExcludes
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No data are currently available
regarding adult life span, survivorship,
and age at first breeding for ashy stormpetrels (Ainley 1995, p. 8). However,
like other procellariids, storm-petrels
are long-lived (Warham 1996, p. 20).
Some ashy storm-petrels reach 25 years
old (Sydeman et al. 1998b, p. 7), and
breeding adults over 20 years in age
have been reported in the closely related
Leach’s storm-petrel (Morse and
Bucheister 1977, p. 344). Mean age of
first breeding in the Leach’s storm-petrel
has been reported at 5.9 years ± 1.3
years (Huntington et al. 1996, p. 19).
Sydeman et al. (1998b, p. 7) concluded
that 90 percent of adult ashy stormpetrels were capable of breeding at 6
years of age.
Marine Environment
Ashy storm-petrels are not as
migratory as other storm-petrel species,
foraging primarily in the California
Current, from northern California to
central Baja California, Mexico; the
birds forage in areas of upwelling,
seaward of the continental shelf, near
islands and the coast (Ainley et al. 1974,
p. 300; Briggs et al. 1987, p. 23; Mason
et al. 2007, p. 60). The California
Current flows along the west coast of
North America, and like three other
major, global, eastern boundary (along
the eastern edges of oceanic gyres and
the western edges of continents)
currents, is characterized by the
upwelling of cool, nutrient-rich waters,
which results in increased productivity
of the ocean (i.e., production of
phytoplankton and zooplankton) in the
region (Hickey 1993, pp. 19-70). The
California Current extends about 190 mi
(300 km) offshore from southern British
Columbia, Canada, to Baja California,
Mexico, and is comprised of a
southward surface current, and a
northward (poleward) undercurrent and
surface countercurrents (Miller et al.
1999, p. 1; Dailey et al. 1993, pp. 8-10).
Upwelling is an oceanographic
phenomenon that involves wind-driven
motion of dense, cooler, and usually
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nutrient-rich water towards the ocean
surface, which replaces the warmer and
usually nutrient-depleted surface water
(Smith 1983, pp. 1-2). Coastal upwelling
replenishes nutrients in the euphotic
zone (zone of water where
photosynthesis occurs), resulting in
increased productivity in higher trophic
levels (position within the food chain)
(Batchelder et al. 2002, p. 37).
Crossin (1974, p. 176) observed ashy
storm-petrels as far north as latitude 49°
N, as far south as latitude 7° S, and
approximately 300 mi (480 km) from
shore near latitude 14° N. However,
Spear and Ainley (2007, p. 7) disputed
these observations and state that these
observations likely represented
misidentified dark-rumped Leach’s
storm-petrels. At-sea observations of
ashy storm-petrels south of Islas San
Benitos, Mexico (latitude 28° N) are
unusual, and most observations of the
species are off the coasts of California
and Baja California Norte, Mexico
(Briggs et al. 1987, p. 23; Ainley 1995,
p. 2). Aerial and boat observations at-sea
confirm that the species is associated
with pelagic (offshore) waters along the
slope of and just seaward of the
Continental Shelf and the Monterey
Submarine Canyon, and less often in
neritic (nearshore) waters (Briggs et al.
1987, p. 23; Mason et al. 2007, pp. 5660; Adams and Takekawa 2008, pp. 1213). Ashy storm-petrels are not known
to be associated with the deeper and
warmer oceanic waters west of the
California Current, unlike the closelyrelated Leach’s storm-petrel (Ainley et
al. 1974, pp. 299-300). Thus, the Service
considers the at-sea geographic
distribution (i.e., marine range) of the
ashy storm-petrel to include waters off
the western coast of North America,
from latitude 42° N (approximately the
California-Oregon State line) south to
latitude 28° N (approximately Islas San
Benitos, Mexico), and approximately 75
mi (120 km) out to sea from mainland
and island coasts. The diet of ashy
storm-petrels has not been extensively
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studied, but likely includes euphausiids
(Euphausia spp., Thysanoessa), other
crustaceans, larval lanternfish,
unidentified fish, fish eggs, and squid
(Warham 1990, p. 186; McChesney
1999, pers. com.; Adams and Takekawa
2008, p. 14).
Summary of Factors Affecting the
Species
Section 4 of the Act (16 U.S.C. 1533)
and implementing regulations at 50 CFR
part 424 set forth procedures for adding
species to the Federal List of
Endangered and Threatened Wildlife. In
making this finding, we summarize
below information regarding the status
and threats to this species in relation to
the five factors in section 4(a)(1) of the
Act. In our 90–day finding for this
petition (73 FR 28080), we organized
potential threats under the five factors
according to how they were organized
and described in the petition. In this
12–month finding, we analyze all of the
potential threats described in the
petition, but have reorganized them
slightly under the factors that more
appropriately categorize them. In
making our 12–month finding, we
considered and evaluated all scientific
and commercial information available,
including information received during
and after the public comment period
that ended July 14, 2008.
Factor A: The Present or Threatened
Destruction, Modification, or
Curtailment of the Species’ Habitat or
Range
Like most other procellariids, ashy
storm-petrels feed mostly offshore or
pelagically (Warham 1990, p. 10; Ainley
1995, p. 2) and return to land to breed
at locations on islands and offshore
rocks protected from mammalian
predators (Warham 1990, p. 13; Ainley
1995, p. 3). Consequently, in this
section, we describe various threats that
may destroy, modify, or curtail the ashy
storm-petrel’s marine and terrestrial
habitats and range. The petitioner
asserts that the ashy storm-petrel is
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being or will be negatively affected by
current and future climate change
(specific effects: reduction in ocean
productivity; ocean acidification; and
sea level rise), tourism (specific effects:
disturbance of habitats and nesting
birds), and introduced grasses (CBD
2007, p. 15). The petitioner further
asserts that the ashy storm-petrel’s atsea foraging habitat is being degraded by
artificial (human-caused) light
pollution, chemical and plastics
pollution, and current and future
oceanic changes related to climate
change resulting from greenhouse gas
emissions (CBD, p. 15); We
addresspotential threats posed by
artificial light pollution and chemical
and plastics pollution under Factor E
below. In this 12–month finding, we
discuss under Factor A the following
potential threats: (1) Climate change and
associated effects—specifically, reduced
productivity, ocean acidification, and
sea-level rise; (2) introduced grasses;
and (3) degradation of nesting habitats
from tourism and military operations.
The petitioner states that global
warming will likely affect the ashy
storm-petrel by causing warmer water
and reduced upwelling, which reduces
primary productivity in the California
current system that would in turn
decrease ashy storm-petrel breeding
success and perhaps survival; global
warming is leading to more intense El
˜
Nino events that could lead to ashy
storm-petrel breeding failures; sea-level
rise will eliminate important ashy
storm-petrel breeding habitat in sea
caves and off-shore rocks in the Channel
Islands; and ocean acidification may
lead to declines in the prey species
upon which petrels depend (CBD 2007,
p 2). We discuss first below the various
climate-related factors affecting ashy
storm-petrels.
˜
El Nino and Reduced Productivity
˜
The term El Nino-Southern
˜
Oscillation (hereafter, El Nino) is used
to describe periodic basin-wide changes
in air-sea interaction in the equatorial
Pacific Ocean region, which result in
increased sea-surface temperatures,
reduced flow of eastern boundary
currents, and reduced coastal upwelling
(Norton and McLain 1994, pp. 16,019–
16,030; Schwing et al. 2002, p. 461). La
˜
Nina events (sometimes called anti-El
˜
Nino or cold-water events) produce
effects in the northeast Pacific Ocean
that tend to be the reverse of those that
˜
occur during El Nino events; during La
˜
Nina events, strong upwelling-favorable
winds and a shallow thermocline (zone
of rapid temperature change with
increased depth that typically separates
warm and cold water) result in colder,
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more nutrient-rich waters than usual
(Murphree and Reynolds 1995, p. 52;
Oedekoven et al. 2001, p. 266). In
addition to inter-annual climate events
˜
˜
such as El Nino and La Nina, the midlatitude Pacific Ocean experiences
warm and cool phases that occur on
decadal time scales (Mantua 2000, p. 2).
The term ‘‘Pacific Decadal Oscillation’’
was coined to describe long-term
climate variability in the Pacific Ocean,
in which there are observed warm and
cool phases, or ‘‘regime shifts’’ (Mantua
et al. 1997, pp. 1069-1079).
The California Current system is
affected by inter-annual (ENSO-related
˜
˜
(El Nino/La Nina)) and inter-decadal
(Pacific Decadal Oscillation) climatic
processes. The petitioner cites
Behrenfeld et al. (2006, pp. 752-755) to
describe significant global declines in
net primary production between years
1997 and 2005, attributed to reduced
nutrient enhancement due to ocean
surface warming (CBD 2007, p. 25).
Specific to the marine range of the ashy
storm-petrel, the petitioner states that
the California Current System has
experienced some of the most welldocumented changes in ocean climate
due to global warming (CBD 2007, p.
25). The petition cites several examples
of changes in the California Current
System, which it attributes to climate
change, that all relate to reduced ocean
productivity, including: reduction in
zooplankton biomass and increased sea
surface temperatures (Roemmich and
McGowan 1995, pp. 1324-1326; Lynn et
al. 1998, pp. 25-49); upwelling of
warmer, nutrient-depleted waters,
which leads to breeding failures,
mortality, and population declines
across trophic levels (Barber and Chavez
1983, pp. 1203-1210); delay in the onset
of spring upwelling (Schwing et al.
2006, pp. 1-5); anomalously warm
water, low nutrient levels, and low
primary production (Thomas and
Brickley 2006, pp. 1-5); reduced
zooplankton biomass (Mackas et al.
2006, pp. 1-7); unprecedented seabird
breeding failures (Sydeman et al. 2006,
pp. 1-5); and anomalously low
recruitment of rocky intertidal
organisms (Barth et al. 2007, pp. 37193724). Specific changes in the California
Current that may negatively affect the
ashy storm-petrel are discussed below.
Roemmich and McGowan (1995, pp.
1324-1326) described 43 years (from
1951 to 1993) of observations off the
southern California coast. They reported
that zooplankton had decreased by 80
percent, and that surface temperatures
taken during transects off Point
Conception and Orange County
(approximately) warmed by an average
of 2.2 °F (1.2 °C) and 2.3 °F (1.6 °C),
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41837
respectively, during this period. They
suggested that the zooplankton decline
was directly related to and caused by
the observed warming (Roemmich and
McGowan 1995, p. 1325). The petitioner
cited Schwing et al. (2006, pp. 1-5),
Barth et al. (2007, pp. 3719-3724), and
Sydeman et al. (2006, pp. 1-5) to
describe a delay in the onset of spring
upwelling in the northern California
Current that resulted in breeding
failures of Cassin’s auklets
(Ptychoramphus aleuticus) at Southeast
Farallon Island, and at Triangle Island,
British Columbia, in 2005 (CBD 2007, p.
25). At Southeast Farallon Island,
Cassin’s auklets also failed to breed in
2006 as well, likely as a result of warmwater conditions, reduced upwelling,
and reduced availability of krill
(Warzybok et al. 2006, pp. 12-14).
At Southeast Farallon Island,
productivity (chicks fledged per
breeding pair) of ashy storm-petrels was
0.56 in 2005, and 0.48 in 2006
(Warzybok et al. 2006, p. 7). At Santa
Cruz Island, productivity of ashy stormpetrels was 0.58 in 2005, and 0.68 in
2006 (McIver et al. in preparation, tables
2-4). Sydeman et al. (2006, p. 1)
reported that euphausiid crustacean
(krill) biomass in the Gulf of the
Farallones was reduced in 2005, but
remained high south of Point
Conception. To successfully raise a
chick, an adult storm-petrel must obtain
enough food for itself, plus one-half the
food requirements of the chick, plus
food to fuel the metabolic costs of
transporting food to the nesting location
(Quinlan 1979, p. 103). Thus, if food
was less available to ashy storm-petrels
foraging north of Point Conception
(presumably, Southeast Farallon Island
breeders) in 2005 and 2006, adverse
affects may have appeared during the
chick stage, and this could explain (in
part) reduced breeding success at
Southeast Farallon Island in 2006.
Like Cassin’s auklets, ashy stormpetrels feed on krill. However, unlike
Cassin’s auklets, ashy storm-petrels
have more extended incubation and
chick-rearing periods (per egg-laying
effort), and feed over a wider geographic
area; thus, they are likely more able to
exploit similar food resources when
these resources are reduced or more
patchily distributed. As stated earlier,
Cassin’s auklets failed to breed in 2005
and 2006, in contrast to ashy stormpetrels, which did breed. Additionally,
Ainley (1990b, pp. 357-359) reported
that ashy storm-petrels showed the
lowest inter-annual variability in
productivity of any species breeding at
Southeast Farallon Island, for the years
1971 to 1983. Ashy storm-petrel
productivity was 0.64 and 0.69 in 1972
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(n = 36) and 1973 (n = 35), respectively;
0.81 in 1976 (n = 37); and 0.75 and 0.67
in 1982 (n = 28) and 1983 (n = 18),
respectively (Ainley and Boekelheide
1990, p. 392). This is of importance
˜
because during this time period, El Nino
events occurred in 1972-73, 1976, and
1982-83 (Ainley 1990a, p. 36). Ainley
(1990b, p. 371) reported that breeding
by other seabirds at Southeast Farallon
Island was poor to nonexistent in 1973,
1976, 1978, 1982, and 1983. As noted
above, ashy storm-petrels were the
exception to this observation; they bred
in all years of the study, and no clear
correlation between warm-water years
and reduced reproductive success
(productivity) was evident for this
species (Ainley and Boekelheide 1990,
˜
p. 392). The only response to El Nino
conditions that may be evident are
smaller numbers of ashy storm-petrels
breeding and delayed egglaying (later in
the season than in other years) (Ainley
and Boekelheide 1990, p. 392; Ainley et
al 1990, pp. 149-150). However, since
regular annual monitoring of nesting
activities began at Southeast Farallon
Island (in 1971) and at Santa Cruz
Island (in 1994), researchers have
observed ashy storm-petrels (on a
population level) breeding each year. In
research conducted in 1995-97 and
2005-07, McIver et al. (in preparation, p.
10) report that reproductive success
(productivity) of ashy storm-petrels at
Santa Cruz Island did not appear to be
˜
negatively affected by El Nino
conditions (although timing of breeding
˜
was later in 1998, an El Nino year), and
no clear relationship between
oceanographic conditions in southern
California and reproductive success of
ashy storm-petrels was observed. As
presented above, this is supported by
data from research at Southeast Farallon
Island. Productivity of ashy stormpetrels at Southeast Farallon Island
declined from the late 1980s to the mid1990s (Sydeman et al. 2001, p. 315; CBD
2007, p. 8; Warzybok and Bradley 2007,
p. 7). However, more recent data
indicate that this decline in productivity
has not continued. Warzybok and
Bradley (2007, p. 17) describe an
analysis of capture-recapture data that
shows increasing capture rates and
increasing survival of ashy storm-petrels
on Southeast Farallon Island. Based on
observed annual breeding and
reproductive success values of ashy
˜
storm-petrels during El Nino events, and
the low inter-annual variability in
reproductive success as reported by
Ainley and Boekelheide (1990, p. 392)
and McIver (2002, p. 29), we conclude
there is no clear relationship between
reduced productivity of phytoplankton
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and zooplankton in the California
˜
Current due to El Nino events and
reproductive success of ashy stormpetrels.
As enumerated above, the petition
cited several examples of changes in the
California Current System, revolving
around ocean productivity, which the
petition claims has had an adverse effect
on ashy storm-petrels. Based on our
review of the available information, we
found that some species of seabirds
have experienced breeding failures in
certain years, which can be linked to El
˜
Nino events, warmer water, or lower
primary productivity. However,
productivity of the ashy storm-petrel
over approximately the past 40 years
does not show breeding failures in those
same years. This is likely due to the
species’ ability to exploit a wider range
of resources than other seabirds. Based
˜
on the species’ response to El Nino
events, we conclude the ashy stormpetrel is not likely to be adversely
affected by potentially lower ocean
productivity due to long-term ocean
warming. In 2006, when Cassin’s
auklets failed to breed at Southeast
Farallon Island likely as a result of
warm-water conditions, reduced
upwelling, and reduced availability of
krill or a delay in the onset of spring
upwelling, ashy storm-petrels did breed
but had slightly lower productivity.
Based on this information, we do not
consider the delay in the onset of spring
upwelling to be a threat to the species.
Therefore, based on the best scientific
information available to the Service
regarding the effects of climate change,
˜
including the effects of El Nino and
changes in the California Current on
ocean productivity, we do not consider
this to be a significant threat to the ashy
storm-petrel at Southeast Farallon
Island, at the Channel Islands, or
rangewide.
Climate Change – Ocean Acidification
The petitioner claims that ocean
acidification may eventually have
detrimental impacts on the ashy stormpetrel’s crustacean prey species (e.g.,
Euphausia pacifica, Thysannoessa
spinifera) that may be impaired in
building their exoskeletons in the
coming decades (CBD 2007, p. 29). The
petitioner cites Orr et al. (2005, p. 682)
that mid-latitude waters, where the
California Current Ecosystem is located,
are experiencing the largest decreases in
surface carbonate ion concentrations.
The chemical processes behind ocean
acidification are well known. The
presence of inorganic carbon in the
ocean is largely responsible for
controlling the pH (the measure of
acidity) of seawater, and dissolved
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inorganic carbon in seawater exists in
three major forms, including a
bicarbonate ion, carbonate ion, and
aqueous carbon dioxide (Fabry et al.
2008, pp. 414-415). Human industrial
and land use activities are resulting in
increased atmospheric concentrations of
carbon dioxide (Feely et al. 2004, p.
362); much carbon dioxide is absorbed
by the oceans (Caldiera and Wickett
2003, p. 365; Sabine et al. 2004, p. 370).
When carbon dioxide dissolves in
water, carbonic acid is formed, most of
which quickly dissociates into a
hydrogen ion and a bicarbonate ion; the
hydrogen ion can further react with a
carbonate ion to form bicarbonate (Fabry
et al. 2008, p. 415). The effects of
increased absorption of carbon dioxide
by the oceans have been given the term
‘‘ocean acidification’’ and include an
increase in concentrations of carbonic
acid, bicarbonate, and hydrogen ions; a
decrease in concentration of carbonate;
and a reduction in the pH level in
seawater (Caldiera and Wickett 2003, p.
365; Royal Society et al. 2005, p.16;
Fabry et al. 2008, p. 415). Pure water has
a pH of 7; solutions below pH 7 are
acidic, and solutions above pH 7 are
alkaline, or basic (summarized in Hardt
and Safina 2008, p. 1). Oceans are
slightly alkaline, with a pH of 8.1 (at
latitude 30°N, approximately; Caldiera
and Wickett 2005, p. 5). Measurements
of surface ocean pH in 2005 were 0.1
unit lower than preindustrial values
(prior to the 1850s) and could become
0.3 to 0.4 units lower by the end of the
21st century (Caldiera and Wickett
2005, p. 5). Marine organisms that
produce shells, such as corals, mollusks,
echinoderms, and crustaceans, require
carbonate ions to produce their calcium
carbonate shells and skeletons (Orr et al.
2005, p. 681; Fabry et al. 2008, p. 415).
There are three mineral forms of
calcium carbonate (magnesium-calcite,
aragonite, and calcite), and each has
different tendencies to dissolve
(solubility) in seawater (summarized in
Hardt and Safina 2008, p. 2). The
reaction of excess carbon dioxide with
seawater reduces the availability of
carbonate ions necessary for shell and
skeleton formation for these organisms
(Fabry et al. 2008, p. 415). Generally,
oceanic surface waters are saturated
with calcium carbonate, deeper waters
are under-saturated, and the depth
where waters transition from saturated
to unsaturated is called the saturation
horizon (summarized in Hardt and
Safina 2008, p. 2). A reduction in
carbonate ions causes all forms of
calcium carbonate to dissolve at
shallower depths, and causes a
reduction in the rate at which marine
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organisms can produce calcium
carbonate (summarized in Hardt and
Safina 2008, p. 2). In other words, once
formed, calcium carbonate will dissolve
back into the water unless the
surrounding seawater contains
sufficiently high concentrations of
carbonate ions (Royal Society et al.
2005, p. 10).
The major planktonic calcium
carbonate producers in the ocean are
coccolithophores (single-celled
phytoplankton), foraminifera (amoeboid
protists), and pteropods (marine
mollusks) (Fabry et al. 2008, p. 417).
Marine organisms act as a ‘‘biological
pump,’’ removing carbon dioxide and
nutrients from the surface ocean and
transferring these elements into the
deeper ocean and ocean bottom
(Zondervan et al. 2001, p. 507; Chen et
al. 2004, p.18).
Feely et al. (2008, pp. 1490-1492)
conducted hydrographic surveys along
the continental shelf of North America,
and found evidence for undersaturated
(with respect to aragonite) and low pH
(less than 7.75) waters at mid-shelf
depths of approximately 131 to 394 feet
(ft) (40 to 120 meters (m)) from about
middle California (latitude 37° N,
approximately) to Baja California Sur,
Mexico (latitude 26° N, approximately).
Feely et al. (2008, p. 1492) reported that
much of the corrosive character of these
waters is natural as the result of
respiration processes at intermediate
depths below the euphotic zone. Feely
et al. (2008, p. 1492) cautioned that the
California coastal region continues to
accumulate anthropogenic carbon
dioxide, and concluded that seasonal
upwelling processes enhance the
advancement of the corrosive deep
water into wide regions of the North
American continental shelf. Feely et al.
(2008, p. 1492) further reported that
little was known about how intermittent
exposure to acidified water might affect
the development of calcifying, or shell
building, organisms in this region.
The ecological effects of changing
ocean carbonate chemistry are uncertain
due to complexities of marine
ecosystems, and research to date has
focused on the impact of acidification
on calcifying organisms (Antarctic
Climate & Ecosystems Cooperative
Research Centre 2008, p. 7). Although
the chemical processes associated with
ocean acidification and the biological
processes involving the transport of
carbon in the oceans have been studied
and described in detail, little research
has been conducted to assess the
response of many zooplankton
populations, including euphausiids
(upon which ashy storm-petrels likely
feed), to ocean acidification (Fabry et al.
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2008, p. 426). However, the Service is
aware of one study (Yamada and Ikeda
1999, pp. 62-67) that experimentally
tested the acute (lethal) effects of
lowered pH levels upon Euphausia
pacifica, a species of krill that occurs in
the northern Pacific Ocean and is a
known prey item of ashy storm-petrels.
Observing 5 juveniles and 20 nauplii
(the free-swimming first stage of the
larva) of Euphausia pacifica, Yamada
and Ikeda (1999, pp. 65) found
increased mortality with increased
exposure time and decreased pH (less
than 6.9). Based on their data, Yamada
and Ikeda (1999, p. 66) also suggested
that the ability to tolerate lowered pH
may be highly variable between and
possibly within species, as in the case
of nauplii and juveniles of Euphausia
pacifica. Yamada and Ikeda (1999, p.
66) suggested that information about pH
levels that induce chronic (sublethal)
effects would be more appropriate to
estimate the long-term consequences for
a given zooplankton population, in that
zooplankton may survive exposure to
lower pH levels but may be unable to
produce normal offspring. The Service
is also aware of research currently being
conducted to study the possible effects
of ocean acidification on euphausiids in
waters near Antarctica (see Rowbotham
2008, p. 1), but this research has just
begun and data are currently not
available (T. Berli, personal
communication 2008).
As stated in the Species Description
section, the diet of ashy storm-petrels
has not been extensively studied;
however, like other species of stormpetrels, ashy storm-petrels likely feed on
euphausiids, juvenile lanternfish, fish
eggs, and other small fish that occur at
the surface of the ocean. Our review of
the available information did not reveal
any information regarding diet studies
or measurements of chick growth and
weight that indicate that ashy stormpetrels are eating fewer euphausiids or
are providing less food to their chicks.
Additionally, our review of the available
information did not find any research
indicating that ocean acidification is
causing acute or chronic effects to
euphausiid populations that occur in
the California Current, or any other
species of krill that occur in the
California Current, on which ashy
storm-petrels feed. Although the
processes and potential effects of ocean
acidification on biological food webs
have been described, and experimental
research on Euphausia pacifica has
tested lethal effects of exposure to low
pH, our review of the available
information did not reveal any evidence
that demonstrates a direct link between
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41839
ocean acidification and reduced
abundance and survival of prey items
on which ashy storm-petrels depend.
Additionally, Ainley (1990b, p. 371)
reported that breeding by other seabirds
at Southeast Farallon Island was poor to
nonexistent during warm-water years
˜
(El Nino events). However, ashy stormpetrels bred in years that other seabird
species did not (Ainley and Boekelheide
1990, p. 392), which is an indication
that the ashy storm-petrel is less
affected by changes in ocean
productivity than other species.
Therefore, based on our review of the
available information, we conclude that
the potential effects of ocean
acidification are not currently a
significant threat to ashy storm-petrels
based on the uncertainty of the
ecological effects of changing ocean
carbonate chemistry.
Published research and oceanographic
modeling does show that oceans are
acidifying, and we recognize that ashy
storm-petrels may be susceptible to
changes in the oceans’ chemistry in the
future. However, based on the best
scientific information available to the
Service regarding ocean acidification, at
this time we do not consider ocean
acidification to be a significant threat to
the ashy storm-petrel at Southeast
Farallon Island, at the Channel Islands,
or rangewide.
Climate Change – Sea Level Rise
The petitioner claims that climate
change will cause rises in the elevation
of the oceans that will have negative
consequences for ashy storm-petrels by
eliminating (presumably, by inundation
and submersion by seawater) important
habitat in sea caves and offshore rocks
in the California Channel Islands (CBD
2007, p. 28). Sea levels along the
California coast are projected to rise
approximately 1 ft (0.3 m) by 2050 and
approximately 3 ft (0.9 m) by 2100
(California Coastal Commission 2001,
pp. 14-15; Cayan et al. 2006, p. S71).
Future sea levels along the coast of
California will likely depend upon (in
part): future changes in global
temperatures; lag time between
atmospheric changes and oceanic
reactions; thermal expansion of ocean
water; effects of atmospheric
temperature changes on Antarctica;
melting of Greenland ice and other
glaciers; and local subsidence and uplift
of coastal areas (California Coastal
Commission 2001, p. 12). Gradual sea
level rises progressively worsen the
impacts of high tides (through erosion
and submersion), surge, and waves
resulting from storms (Cayan et al. 2008,
pp. S57-S58).
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We reviewed topographic maps and
information provided in Sowls et al.
(1980), Bunnell (1988), and Carter et al.
(1992; 2006a; 2006b) to estimate the
range of elevations above sea level of
suitable ashy storm-petrel habitat at
each of the 26 known breeding locations
(Table 3).
TABLE 3. ESTIMATED RANGE OF ELEVATION ABOVE SEA LEVEL (ASL) IN FEET (FT) AND METERS (M) OF KNOWN NESTING
HABITAT OF ASHY STORM-PETRELS.
Breeding Location Name
1 ...........................
2 ...........................
3 ...........................
4 ...........................
5 ...........................
6 ...........................
7 ...........................
8 ...........................
9 ...........................
10 .........................
11 .........................
12 .........................
13 .........................
14 .........................
15 .........................
16 .........................
17 .........................
18 .........................
19 .........................
20 .........................
21 .........................
22 .........................
23 .........................
24 .........................
25 .........................
26 .........................
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Location
Number
Bird Rock near Greenwood, Mendocino County ......................................................................
Caspar, near Point Cabrillo, Mendocino County ......................................................................
Bird Rock, Marin County ..........................................................................................................
Stormy Stack, Marin County .....................................................................................................
Southeast Farallon Island .........................................................................................................
Castle/Hurricane Colony Complex, Monterey County ..............................................................
Castle Rock, Santa Barbara County ........................................................................................
Prince Island .............................................................................................................................
Shipwreck Cave, Santa Cruz Island .........................................................................................
Dry Sandy Beach Cave, Santa Cruz Island .............................................................................
Del Mar Rock, Santa Cruz Island .............................................................................................
Cave of the Birds Eggs, Santa Cruz Island .............................................................................
Diablo Rocks, Santa Cruz Island .............................................................................................
Orizaba Rock, Santa Cruz Island .............................................................................................
Bat Cave, Santa Cruz Island ....................................................................................................
Cavern Point Cove Caves, Santa Cruz Island .........................................................................
Scorpion Rocks, Santa Cruz Island .........................................................................................
Willow Anchorage Rocks, Santa Cruz Island ...........................................................................
Gull Island, Santa Cruz Island ..................................................................................................
Santa Barbara Island ................................................................................................................
Sutil Island ................................................................................................................................
Shag Rock ................................................................................................................................
Ship Rock, Santa Catalina Island .............................................................................................
Seal Cove Area, San Clemente Island ....................................................................................
Islas Los Coronados, Mexico ...................................................................................................
Islas Todos Santos, Mexico .....................................................................................................
The nesting habitat at the majority of
ashy storm-petrel breeding locations
will likely not be affected by the sea
level rise projected for California by
2100 (Table 3). Some nesting habitat at
only one location at Cavern Point Cove
Caves, Santa Cruz Island, would likely
be submerged if projected sea level rises
of 1 ft (0.3 m) by 2050 occur; much of
the nesting habitat at this location
would likely be submerged if the sea
level rises 3 ft (0.9 m) by year 2100.
Prior to the mortality event in 2008 at
this location (see Factor C), Cavern
Point Cove Caves had approximately 40
breeding birds annually. Some habitat at
other cave locations on Santa Cruz
Island may be susceptible to submersion
by seawater. For example, on Santa Cruz
Island in November 2008, McIver et al.
(2009, p. 6) reported flooding by ocean
water in a sea cave that likely killed one
storm-petrel chick. Despite this unusual
event, the majority of the nesting habitat
in the sea caves at Santa Cruz Island
occurs greater than 3 ft (1 m) above
current sea level, and would not likely
be submerged during breeding season
months (April through November)
within the next 40 to 50 years. Winter
storm surges periodically wash all of the
sea caves at Santa Cruz Island, but these
storm events likely do not negatively
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Elevation ASL
affect ashy storm-petrels, since most
ashy storm-petrels are not attending the
colonies during winter months (Ainley
1995, p. 5). In fact, past winter storms
have benefited ashy storm-petrels at
Santa Cruz Island by creating nesting
habitat; approximately 25 percent of
ashy storm-petrel nest sites in Bat Cave
occur among accumulated driftwood
debris (both human-made and natural)
that has washed into the cave during
past winter storm events.
Based on information available to the
Service regarding elevations (above
current sea level) of breeding locations
of ashy storm-petrels, and projected
estimates of sea level rise along the west
coast of North America during the 21st
century, we conclude that a small
portion of the total population of ashy
storm-petrels (approximately 0.8
percent) could be negatively affected by
rising sea levels by 2050. Therefore,
based on the best scientific information
available to the Service regarding
climate change-induced sea level rise, at
this time we do not consider this to be
a significant threat to the ashy stormpetrel at Southeast Farallon Island, at
the Channel Islands, or rangewide.
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10–40 ft (3–12 m)
10–40 ft (3–12 m)
10–40 ft (3–12 m)
10–50 ft (3–15 m)
10–330 ft (3–100 m)
10–100 ft (3–30 m)
20–80 ft (6–24 m)
20–300 ft (6–91 m)
5–15 ft (1.5–5 m)
5–15 ft (1.5–5 m)
5–20 ft (1.5–6 m)
5–10 ft (1.5–3 m)
10–40 ft (3–12 m)
10–30 ft (3–9 m)
5–20 ft (1.5–6 m)
0–10 ft (0–3 m)
10–40 ft (3–12 m)
10–40 ft (3–12 m)
10–100 ft (3–30 m)
10–600 ft (3–183 m)
10–250 ft (3–76 m)
10–50 ft (3–15 m)
5-20 ft (1.5–6 m)
10-50 ft (3–15 m)
10-100 ft (3–30 m)
10-100 ft (3–30 m)
Changes in Terrestrial Breeding Habitat
Introduced Grasses
The petitioner asserts that the ashy
storm-petrel’s island breeding habitats
are being modified and degraded by
introduced species and specifically, that
introduced grasses have increased at
Southeast Farallon Island, causing some
nesting areas to be unusable for ashy
storm-petrels (CBD 2007, p. 30). In
addition, the petitioner claims that
introduced grasses are widespread at all
ashy storm-petrel colonies and that their
effects have not been evaluated (CBD
2007, p. 30). Ainley (1995, p. 9)
describes introduced grasses as a factor
potentially limiting the amount of
available nesting habitat for ashy stormpetrels at Southeast Farallon Island.
Ainley and Hyrenbach (in press, p. 12)
report that introduced grasses have
spread, thickened, and grown among the
talus slopes at Southeast Farallon
Island, and suggest that grasses likely
limit access to cavities by ashy stormpetrels, which do not excavate nesting
burrows and instead rely upon available
nesting crevices. However, the
petitioner did not provide, nor did our
review of the available information
reveal, specific information that
quantifies the amount of suitable
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nesting habitat at Southeast Farallon
Island, or other breeding locations, that
may be unavailable to ashy stormpetrels because of introduced grasses. In
addition, our review of the available
information found no information to
indicate that introduced grasses are
widespread at all breeding locations.
For example, grasses do not occur in sea
caves or on most offshore rocks where
ashy storm-petrels nest.
Introduced grasses may occur in
proximity to ashy storm-petrel nest sites
on Southeast Farallon Island and on
Santa Barbara Island. Based on
population estimates for these areas
presented in Table 1, approximately 51
to 64 percent of ashy storm-petrels
breed at these locations; however, we
are not aware of any evidence through
direct observation or vegetation surveys
that indicates that introduced grasses
prevent significant numbers of ashy
storm-petrels from nesting. Grasses are
widespread on Santa Barbara Island,
where the major plant communities
include island grassland, coastal sage
scrub, maritime desert scrub, and
coastal bluff scrub (Schoenherr et al.
2003, p. 349). However, ashy stormpetrels at Santa Barbara Island likely
nest in crevices that occur in steep
cliffs, where grasses are less common
(Carter et al. 1992, p. I-81). Therefore,
based on the best scientific information
available to the Service regarding the
threat of introduced grasses, at this time
we do not consider this to be a
significant threat to the ashy stormpetrel at Southeast Farallon Island, at
the Channel Islands, or rangewide.
Human Degradation of Nesting Habitats
The petitioner states that human
disturbance and degradation of nesting
habitats through tourism and military
activities threaten the continued
existence of the ashy storm-petrel (CBD
2007, p. 35). Regarding tourism, most
breeding locations occur on federally
owned or managed lands that are
generally inaccessible to visitation by
the public. Southeast Farallon Island
contains approximately 36 to 53 percent
of the total ashy storm-petrel population
and has low human visitation by the
Service’s Refuge staff but is closed to the
general public. Due to steep topography
and difficult ocean and landing
conditions, breeding locations on
islands and offshore rocks other than
Southeast Farallon Island are generally
inaccessible to tourists, and our review
of the available information has not
revealed specific information indicating
that ashy storm-petrel nesting habitats
on islands, offshore rocks, and islets are
being degraded by human visitation. Sea
caves on Santa Cruz Island are
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14:26 Aug 18, 2009
Jkt 217001
susceptible to visitation by tourists (e.g.,
sea kayakers) (McIver 2002, p. 53;
McIver et al. 2008, pp. 7-8). However,
the U.S. National Park Service, Channel
Islands National Park (Park) has closed
two sea caves to the public, and in
spring 2009, installed signs
(inconspicuous from the water) within
the entrances of Bat Cave and Cavern
Point Cove Caves informing tourists that
the caves contain nesting seabirds and
are closed to visitation by the public (W.
McIver, personal observation). Although
there is direct evidence that tourists
have occasionally visited sea caves at
Santa Cruz Island where ashy stormpetrels nest (McIver et al. 2008, p. 5;
McIver et al. 2009, pp. 7-8), the
available information does not indicate
adverse impacts of tourism upon ashy
storm-petrels, such as dead birds,
broken eggs, or degraded or modified
nesting habitats. Due to observed lower
hatching success at Cavern Point Cove
Caves, in comparison to other locations
at Santa Cruz Island (McIver 2002, p.
24), we cannot discount the possibility
that visitation by tourists may have
resulted in disturbance to and
abandonment of some nests of ashy
storm-petrels at this location. However,
because most ashy storm-petrel breeding
locations are generally inaccessible to
tourists, we find it unlikely that human
visitation has caused large-scale
disturbance to ashy storm-petrels and
subsequent abandonment of nesting
efforts. Thus, based on land ownership
and restricted human activities at ashy
storm-petrel breeding locations on
Southeast Farallon Island and on the
Channel Islands, we find human
tourism is currently not a substantial
threat to the ashy storm-petrel at
Southeast Farallon Island, at the
Channel Islands, or rangewide.
Within the range of the ashy stormpetrel, military activities only occur on
San Clemente Island, which is one of
the Channel Islands. San Clemente
Island is owned and managed by the
Department of the Navy, and it is
estimated that at least 10 ashy stormpetrels breed there (H. Carter and D.
Whitworth,). Ashy storm-petrels are
known to breed at Seal Cove Rocks
(Carter et al. 2008a, p. 119), off the
island’s west side, and may breed on
offshore rocks off China Point, and at or
near Mosquito Cove (Hering 2008, p.4).
Seal Cove Rocks occur outside of any
current training areas (Hering 2005, p.
5). Offshore rocks near China Point do
occur within the Shore Bombardment
Area (SHOBA); however, these rocks are
not targeted by bombardment activities,
and ashy storm-petrels have not been
confirmed as breeding there (Hering
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41841
2008, p. 5). Mosquito Cove is also
within the boundaries of SHOBA, but
occurs outside the impact areas (Hering
2008, p. 5). Carter et al. (2008c, pp.1213) report that portions of Prince Island
were used by the U.S. Navy as a target
for aerial bombing and missile testing
from the late 1940s to the early 1970s.
Carter et al. (2008c, p.13) speculated
that effects included: some seabirds
probably were killed by explosions; loss
of breeding habitats for burrow- and
crevice-nesting seabirds likely occurred
due to explosions; and periodic human
disturbance of seabirds likely occurred
from military personnel. However, our
review of the available information did
not reveal any specific impacts to ashy
storm-petrels at Prince Island as a result
of these activities, and these activities
have not occurred at this breeding
location for more than 35 years.
Therefore, because only a small
percentage (approximately 0.1 percent)
of the entire population of ashy stormpetrels nests on San Clemente Island,
current military activities at San
Clemente Island likely do not affect
ashy storm-petrel nesting areas there,
and because military activities no longer
occur at Prince Island, we conclude that
military activities do not pose a
substantial threat to the ashy stormpetrel at Southeast Farallon Island, at
the Channel Islands, or rangewide.
Human visitation at Southeast
Farallon Island is low, and there is no
evidence to suggest degradation of
nesting habitats there. At the Channel
Islands, human visitation is greater near
breeding habitat, but the National Park
Service has taken steps to close several
sea caves where ashy storm-petrels
breed. Additionally, there is no direct
evidence of human impacts to ashy
storm-petrels or their breeding habitat at
these locations. Within the range of the
ashy storm-petrel, military activities
only occur currently on San Clemente
Island but are not targeted at breeding
or nesting areas. Therefore, based on the
best scientific information available to
the Service, at this time we conclude
that human degradation of nesting
habitats by tourism and military
activities is not a significant threat to
the ashy storm-petrel at Southeast
Farallon Island, at the Channel Islands,
or rangewide.
Summary of Factor A
While there is some evidence to
suggest the timing of ashy storm-petrel
egg laying may be delayed as a result of
˜
El Nino events, and that fewer numbers
of ashy storm-petrels may attempt to
˜
breed during El Nino years, these results
do not appear significant, and we have
˜
no information to suggest that El Nino
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events otherwise significantly affect
ashy storm-petrel reproductive success
or productivity, unlike in other sea
birds. Additionally, based on the
˜
species’ response to El Nino events, we
conclude the ashy storm-petrel is not
likely to be adversely affected by
potentially lower ocean productivity
due to long-term ocean warming. Based
on our review of current research, there
is demonstrated evidence of ongoing
ocean acidification; however, current
research does not demonstrate a direct
link between ocean acidification and
reduced abundance and survival of prey
items on which ashy storm-petrels
depend, nor does current research
indicate that reproductive success of
ashy storm-petrels is affected by ocean
acidification. Projected changes in sea
levels along the west coast of North
America (by year 2050) may submerge
nesting habitat at Cavern Point Cove
Caves in the California Channel Islands,
which could affect approximately 0.8
percent of all ashy storm-petrels, but the
majority of currently available nesting
habitat in California will not be affected
by the sea level rise projected in
California during the 21st century. The
Service finds that there is no specific
evidence indicating that the presence of
introduced grasses at Southeast Farallon
Island, the Channel Islands, or other
breeding locations prevents ashy stormpetrels from breeding. Although there is
evidence of some human visitation to
sea caves on Santa Cruz Island,
modification or degradation of nesting
habitat by tourism activities is not a
significant threat to the ashy stormpetrel because of protective measures
taken by the National Park Service and
the lack of evidence of human
disturbance in sea caves on the Channel
Islands. Additionally, military activities
are not a significant threat to the species
because military activities do not occur
at known breeding areas. Therefore,
based on the best available scientific
information, we conclude that the ashy
storm-petrel is not threatened by the
present or threatened destruction,
modification, or curtailment of its
habitat or range at Southeast Farallon
Island, at the Channel Islands, or
rangewide.
Factor B: Overutilization for
Commercial, Recreational, Scientific, or
Educational Purposes
The petitioner stated that research
activities may impact ashy stormpetrels, but also stated there was no
evidence that this impact has had
significant negative consequences on
studied populations (CBD 2007, p. 30).
Our review of the available information
does not indicate that research activities
threaten ashy storm-petrels across all or
a significant portion of their range.
Commercial Purposes
The ashy storm-petrel is not a
commercially exploited or used species.
We are not aware of any information
that indicates that overutilization for
commercial purposes threatens the ashy
storm-petrel across all or in any portion
of its range.
Recreational Purposes
Ashy storm-petrels are a species of
interest during pelagic bird-watching
trips off the coast of California. Ashy
storm-petrels are generally wary of and
avoid boats, including boats with
birdwatchers, and it is highly unlikely
that ashy storm-petrels are negatively
affected by these recreational activities.
Tourism at sea caves (see Factor A)
located on Santa Cruz Island is a
recreational activity that could affect
ashy storm-petrels. However, as stated
above, there is no evidence to suggest
such recreational activities are
significantly affecting the species. We
are not aware of any information that
indicates that overutilization for
recreational purposes threatens the ashy
storm-petrel across all or any portion of
its range.
Scientific and Educational Purposes
The Service is aware of 220 ashy
storm-petrel eggs and 355 study skins
(includes study skins, skeletons, round
skins) that have been collected and
salvaged from 1885 to 2004 for scientific
archival purposes. The Service obtained
data from individual institutions and
records held in the following
institutions and accessed through the
ORNIS data portal (https://ornisnet.org)
on September 23, 2008 (Table 4).
TABLE 4. INSTITUTIONS THAT POSSESS COLLECTED SKINS OR EGGS OF THE ASHY STORM-PETREL.
Number of
skins
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Institution or Entity
California Academy of Sciences, San Francisco, CA .................................................................................................
Cornell University Museum of Vertebrates, Ithaca, NY ..............................................................................................
Delaware Museum of Natural History, Wilmington, DE ..............................................................................................
Field Museum, Chicago, IL ..........................................................................................................................................
Harvard University Museum of Comparative Zoology, Cambridge, MA .....................................................................
Humboldt State University Natural History Museum, Arcata, CA ...............................................................................
Los Angeles County Museum of Natural History, Los Angeles, CA ...........................................................................
Museum of Vertebrate Zoology, Berkeley, CA ............................................................................................................
National Museum of Natural History, Washington, DC ...............................................................................................
Santa Barbara Museum of Natural History, Santa Barbara, CA ................................................................................
San Diego Natural History Museum, San Diego, CA .................................................................................................
Slater Museum of Natural History, Tacoma, WA ........................................................................................................
University of Arizona Museum of Natural History, Tucson, AZ ..................................................................................
University of California at Los Angeles - Dickey Collection, Los Angeles, CA ..........................................................
University of Kansas Natural History Museum and Biodiversity Research Center, Lawrence, KS ...........................
University of Washington - Burke Museum of Natural History ...................................................................................
Western Foundation of Vertebrate Zoology, Camarillo, CA ........................................................................................
All .................................................................................................................................................................................
In addition, for purposes of measuring
eggshell thickness and organochlorine
(chlorinated hydrocarbon)
contamination, a total of 26 eggs have
been collected from Southeast Farallon
Island, and a total of 68 eggs of ashy
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14:26 Aug 18, 2009
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storm-petrels have been collected and
salvaged from Santa Cruz Island,
between 1968 and 2008 (Coulter and
Risebrough 1973, p. 254; Kiff 1994, p.
11; Welsh and Carter ) and in 2008
(McIver et al. 2009, p. 8). The majority
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181
2
1
10
6
2
18
39
32
13
31
3
9
3
1
3
1
355
Number of
eggs
70
0
0
0
0
2
0
20
6
5
0
3
0
0
0
2
112
220
of ashy storm-petrel birds and eggs that
occur in scientific collections were
collected at Southeast Farallon Island in
the first half of the 20th century. More
ashy storm-petrel birds and eggs were
collected in 1911 (n = 120 specimens)
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than in any other year. Over a period of
124 years, an average of 2.6 ashy stormpetrel eggs per year and 2.9 birds per
year have been collected over most of
the geographic range of the species. The
Service concludes that this low rate of
collection, based on an estimated
population size of 7,000 to 13,000 total
birds, does not constitute a significant
threat to the species.
In California, scientific research
(monitoring of nesting success, mark
and recapture using mist nets, radio
telemetry) has been conducted on
Southeast Farallon Island since the mid1960s (James-Veitch 1970; Ainley et al.
1974, pp. 295-310; Ainley et al. 1990,
pp. 128-162; Sydeman et al. 1998a, pp.
438-447; PRBO Conservation Science),
at Santa Cruz Island since the mid1990s (McIver 2002, pp. 1-70; McIver
and Carter 2006, pp. 1-6; Carter et al.
2007, pp. 4-20; McIver et al. 2008, pp.
1-22; McIver et al. 2009, pp. 1-30), and
at Santa Cruz and Santa Barbara Islands
in 2004 and 2005 (Adams and Takekawa
2008, pp. 9-17). The Service is aware of
the following disturbance (by
researchers) of ashy storm-petrels:
reduced hatching success at Southeast
Farallon Island caused by handling of
birds (James-Veitch 1970, p. 246); and
reduced hatching success at Southeast
Farallon Island in 1977 when
‘‘researcher disturbance was great’’
(Ainley et al. 1990, p. 161). Generally,
however, researchers at both Southeast
Farallon Island and Santa Cruz Island
have implemented procedures to reduce
possible disturbance to ashy stormpetrels during regular nest monitoring
activities. Consequently, we find it
unlikely that scientific studies have
resulted in substantial disturbance of
ashy storm-petrels.
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Summary of Factor B
Our review of the available
information does not indicate that
commercial or recreational
overutilization is a threat to the ashy
storm-petrel. We are aware of the long
history of scientific and educational
collecting of ashy storm-petrel skins and
eggs over the past 124 years. However,
the amount and rate of collection does
not represent a significant loss to the
overall population of ashy storm-petrels
rangewide, or in specific breeding
locations. In addition, we have found
that ashy storm-petrels are not currently
negatively affected by scientific
research. Therefore, based on the best
available scientific information, we
conclude that the ashy storm-petrel is
not threatened by overutilization for
commercial, recreational, scientific, or
educational purposes at Southeast
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14:26 Aug 18, 2009
Jkt 217001
Farallon Island, at the Channel Islands,
or rangewide.
Factor C: Disease or Predation
The petitioner asserts that predation
by native predators, including western
gulls, burrowing owls, barn owls,
common ravens, peregrine falcons, deer
mice, and island spotted skunks, impact
ashy storm-petrel populations (CBD
2007, pp. 30-32). In addition, the
petitioner asserts that nonnative
predators, including house mice, black
rats (Rattus rattus), and feral cats (Felis
catus) affect ashy storm-petrel
populations (CBD 2007, pp. 30-32).
As described in the Species
Description section, native avian
predators of the ashy storm-petrel
include western gulls, burrowing owls,
peregrine falcons, and common ravens.
Native mammalian predators of ashy
storm-petrel eggs and birds include deer
mice and island spotted skunks. Known
nonnative mammalian predators of ashy
storm-petrel eggs and birds include
house mice and feral cats (Ainley et al.
1990, p. 156; McChesney and Tershey
1998, p. 341). The black rat is a
potential nonnative predator
(McChesney and Tershey 1998, p. 342),
although predation of ashy storm-petrels
by rats has not been documented.
Predation can affect reproductive
performance of storm-petrels during
incubation and chick-rearing. Because
ashy storm-petrel adults share egg
incubation duties, the death of one adult
of a breeding pair during the incubation
stage could result in incomplete
incubation and failure of the egg to
hatch. Similarly, the death of one adult
of a breeding pair of storm-petrels
during the chick-rearing stage could
result in death of the chick (by
starvation or lack of brooding),
especially if the chick is younger than
about 50 days old (Mauck et al. 2004, p.
883).
Southeast Farallon Island – Avian
Predation
The western gull and burrowing owl
are the primary avian predators of ashy
storm-petrels at Southeast Farallon
Island (Sydeman et al. 1998a, pp. 445446; PRBO Conservation Science).
Approximately 30 percent of the world
population of western gulls nests at
Southeast Farallon Island (Penniman et
al. 1990, p. 219). During the 1996 to
2006 period, the western gull breeding
population at Southeast Farallon Island
has been estimated at about 18,000
breeding birds (Service 2008, p. 42). The
distribution of western gull nesting
areas at Southeast Farallon Island has
shifted and expanded since they were
first mapped in 1959 (Ainley and Lewis
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1974, p. 439; Penniman et al. 1990, p.
224), and since 1976, western gulls have
nested densely over nearly the entire
island, including Lighthouse Hill,
which is considered prime ashy stormpetrel breeding habitat on Southeast
Farallon Island (Ainley and Lewis 1974,
p. 435; Ainley et al. 1990, p. 158;
Sydeman et al. 1998a, p. 446).
The petitioner includes burrowing
owls in its list of predators for the ashy
storm-petrel but includes no
information documenting a threat from
burrowing owls (CBD 2007, p. 30).
Burrowing owls do not breed on
Southeast Farallon Island, but are
regular fall migrants, and a few
individuals (two to five per year, on
average) overwinter at the island
(DeSante and Ainley 1980, p. 30;
Service 2008, p. 50). In the fall,
burrowing owls at Southeast Farallon
Island feed upon nonnative house mice
when mice are seasonally abundant
(Service 2008, p. 50). In late winter and
early spring, after the mouse population
at Southeast Farallon Island declines in
numbers, burrowing owls prey upon
storm-petrels, which are courting and
prospecting for nesting sites (PRBO
Conservation Science; Service 2008, p.
50). To reduce this cause of mortality,
the Farallon National Wildlife Refuge
has trapped and moved to the mainland
several burrowing owls (Service 2008, p.
50). Additionally, the Service is
developing a plan to eradicate the
nonnative house mouse through
rodenticide application and prevent
future human introductions of mice (see
Factor D: Inadequacy of Existing
Regulatory Mechanisms below).
In the following discussion, we assess
avian predation as a possible factor
affecting the ashy storm-petrels by
evaluating information on ashy stormpetrel productivity and mortality on
Southeast Farallon Island and Santa
Cruz Island. Sydeman et al. (2001, p.
315) reported that, among seabird
species at Southeast Farallon Island
laying a single-egg clutch each year, the
ashy storm-petrel showed a significant
pattern of change in reproductive
performance, which increased through
the mid-1980s, then decreased through
1997. Specifically, Sydeman et al.
(2001, p. 317) reported that reduced
reproductive performance of ashy
storm-petrels in his model was related
to significant changes in fledging
success (numbers of chicks fledged per
chicks hatched). Sydeman et al. (2001,
p. 317) also concluded that hatching
success in the 1990s was low and likely
responsible for the decline in stormpetrel reproductive performance during
that time period. An examination of
values of productivity (fledged chicks
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per adult pair) of ashy storm-petrels at
Southeast Farallon Island from 1971
through 2007 (see Table 2) shows
variability in fledging success.
Specifically, Ainley and Boekelheide
(1990, p. 392) reported an average of
0.69 ashy storm-petrel chicks per pair
from 1972 to 1983, Sydeman et al.
(1998b, pp. 42-43) reported 0.74 chicks
per pair using data from 1971 and 1972
and 1992, and Warzybok and Bradley
(2007, p. 24) reported 0.54 chicks per
pair using yearly data from 1996
through 2007 (and noted that
productivity was higher in 2007 (0.53)
than in 2006 (0.46)). These averages
demonstrate variation in productivity
over time, but only Sydeman’s (2001)
study provides a statistical analysis
demonstrating a quadratic trend.
Further, based on our review of the best
available data (see discussion below),
we do not believe that these
productivity values are associated with
lower numbers of ashy storm-petrels.
Ainley et al. (1974, p. 307) and Ainley
et al. (1990, p. 157) estimated stormpetrel mortality rates based on presence
of storm-petrel remains and storm-petrel
bands found in gull pellets collected in
1971 and 1972. Sydeman et al. (1998b,
pp. 1-74) collected wings of storm-petrel
carcasses found on the southwestern
slope of Lighthouse Hill from 1994
through 1996. In 2000, PRBO
Conservation Science searched for and
collected storm-petrel wings on
Lighthouse Hill and other areas on
Southeast Farallon Island, and
categorized collected wings by type of
avian predation (such as gull or owl). In
both studies, wings (which were used as
a measure of predation) were collected
during the course of frequent nestmonitoring activities. Ainley et al.
(1974, p. 307) and Ainley et al. (1990,
p. 157) estimated that about one percent
of the storm-petrel population
(including ashy and Leach’s stormpetrels) on Southeast Farallon Island
were depredated by western gulls in
1971 and 1972. Sydeman et al. (1998b,
pp. 21-22) estimated that 22 ashy stormpetrels were preyed upon by avian
predators per year from 1994 through
1996 on Lighthouse Hill. In addition,
Sydeman et al. (1998b, p. 21) estimated
a 2.5 percent annual mortality rate of
breeding ashy storm-petrels at
Lighthouse Hill due to avian predation
during the period 1994 to 1996, based
on an estimated breeding population of
651 ashy storm-petrels at Lighthouse
Hill. From January 2003 through August
2008, approximately 98 percent of ashy
storm-petrel kills thought to be due to
avian predation on Southeast Farallon
Island occurred between February and
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August, when stratified by month
(PRBO Conservation Science). Average
annual total number of ashy stormpetrels killed during January 2003
through August 2008 was 114 total
individuals. If birds on Southeast
Farallon Island numbered the same as
they did in 1972 (6,461 individuals) or
1992 (4,284 individuals), this level of
predation would be 1.8 percent or 2.7
percent of the population, respectively;
however, these estimates are
speculative.
Estimates of ashy storm-petrel
mortality rates at Southeast Farallon
Island are highly dependent upon
estimated population sizes. Ashy stormpetrels are nocturnal in their visits to
breeding colonies and breed mainly in
deep crevices that are inaccessible to
researchers, and so it is difficult to
obtain direct population counts of the
species. Consequently, estimates of
population size of storm-petrels are
often obtained using capture-recapture
techniques (for example, Sydeman et al.
1998a, pp. 438-447). For the years 1971,
1972, and 1992, Sydeman et al. (1998a,
p. 442) provided estimates for the total
population (non-breeders and breeders)
and the breeding population of ashy
storm-petrels at Southeast Farallon
Island proper and at Lighthouse Hill on
Southeast Farallon Island, an area
considered prime ashy storm-petrel
nesting habitat. Based on a comparison
of data from 1972 and 1992, PBRO
scientists indicated a decline of 22 to 66
percent (95 percent confidence interval)
for total and breeding populations over
the 20–year period for Lighthouse Hill,
the sampling location considered most
reliable for estimation of population size
and population change (Sydeman et al.
1998a, p. 443). We interpret these
results cautiously because they are
based on two data points: one from 1972
and one 20 years later, from 1992. We
hesitate to consider these results
conclusive because animal populations
can undergo cycles, peaks, or troughs
that 2 years of data separated by 20
years cannot capture. Population
estimates were also imprecise owing to
large standard errors (for example,
population estimates for one area ranged
from 660 plus or minus 423 to 1,013
plus or minus 937; Sydeman et al.
1998a, p. 443).
Using preliminary analyses of more
recent data of ashy storm-petrels
captured in mist nets from 1999 through
2007, PRBO scientists state that the
Southeast Farallon Island population
may have increased in years subsequent
to Sydeman’s (1998a) study (Warzybok
et al. 2006, p. 16; Warzybok and Bradley
2007, p. 17). Using data from 1999 to
2007, Warzybok and Bradley (2007, p.
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17) describe an analysis of capturerecapture data that shows increasing
capture rates and increasing survival of
ashy storm-petrels. The authors also
note that there were a greater number of
occupied nesting sites than in previous
years, although this observation could
have been influenced by a change in
monitoring techniques (Warzybok and
Bradley 2007, p. 17). Warzybok and
Bradley’s (2007) report does not
consider the proportion of birds caught
that are nonbreeders, or potential
changes in recapture probabilities
through time; however, their report
represents the most up-to-date
information available at this time. Taken
together, the results of Warzybok and
Bradley’s (2007) analyses suggest an
increasing population of ashy stormpetrels. There are weaknesses in both
the more recent reports that are not
peer-reviewed (Warzybok et al. (2006)
and Warzybok and Bradley (2007)) and
the older report by Sydeman et al
(1998a), which is based on two data
points (one from 1972 and one 20 years
later from 1992). Nevertheless, the
Sydeman et al. (1998a), Warzybok et al.
2006, and Warzybok and Bradley (2007)
studies are the best available
assessments of population trends of
ashy storm-petrels for the time periods
they analyzed. The Warzybok et al.
(2006) and Warzybok and Bradley
(2007) reports contain data we consider
most relevant to this status review
because they were collected more
recently than Sydeman et al.’s (1998a)
data, they include 8 consecutive years of
mark-recapture data, and they describe
empirical observations of occupied nest
sites in addition to statistical estimates
of population trend and survival rate.
The authors note that their study does
not consider the proportion of birds
caught that were nonbreeders or
potential changes in recapture
probabilities through time.
Additionally, they noted an alteration in
monitoring methods that made it
difficult to determine whether increased
occupancy was a result of greater
reproductive effort or due to an increase
in the ability to detect ashy stormpetrels (Warzybok and Bradley 2007, p.
17). While we do not dispute the
historic population decline indicated by
Sydeman et al (1998a), we believe that
the updated information presented in
Warzybok and Bradley’s (2007, p. 17)
preliminary analysis is more indicative
of current population trends on
Southeast Farallon Island.
In an unpublished report, Sydeman et
al. (1998b, p. 21) concluded that an
annual adult ashy storm-petrel survival
probability of 86.7 percent would
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explain the 2.87 percent annual
decrease in population size of ashy
storm-petrels on Southeast Farallon
Island (reported in Sydeman et al.
1998a, p. 443). Based on comparisons to
adult survival estimates in research of
other storm-petrel species, Sydeman et
al. (1998b, pp. 21-22) presumed that an
annual adult survival probability of 89.2
percent would maintain ashy stormpetrel population stability, and
postulated that elimination of all gull
predation would decrease adult
mortality by 2.53 percent, potentially
producing a stable population of ashy
storm-petrels on Southeast Farallon
Island. In populations of such long-lived
organisms as seabirds, annual adult
survival has been reported as the key
parameter having the greatest influence
on population growth rates in
population models of seabirds (S#ther
and Bakke 2000, p. 648; Cuthbert et al.
2001, p. 168; Doherty et al. 2004, p.
606).
Based on information on storm-petrel
wings collected from Southeast Farallon
Island from 2003 through 2008 (PRBO
Conservation Science), approximately
98 percent of avian predation upon ashy
storm-petrels on Southeast Farallon
Island has occurred from February
through August; this corresponds to the
time of year of peak visitation by adults
for breeding purposes and non-breeding
birds prospecting for sites (James-Veitch
1970, p. 71; Ainley 1995, p. 5). During
2003 to 2008, avian predation
categorized as gull, owl, and
‘‘unknown’’ accounted for
approximately 57.4 percent, 34.3
percent, and 8.3 percent, respectively, of
ashy storm-petrel deaths on Southeast
Farallon Island (PRBO Conservation
Science). This raw data allows us to
infer that gulls are likely the greatest
cause of ashy storm-petrel predation on
Southeast Farallon Island.
Avian predation upon ashy stormpetrels at Southeast Farallon Island has
probably occurred continually for
decades. Based on recent reports
showing possible increases in ashy
storm-petrel survival and numbers
(Warzybok and Bradley 2007, p. 17), we
have no indication that such predation
is impacting the population on
Southeast Farallon Island or rangewide.
We conclude that, since ashy stormpetrel populations appear to be
increasing in the presence of such
predation, we have no reason to believe
that such predation will cause a change
in that trend.
Southeast Farallon Island – House Mice
The petitioner cites Ainley et al.
(1990, pp. 128-163) to support its claim
that depredation of ashy storm-petrel
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eggs and chicks by nonnative house
mice is the leading cause of egg failure
and chick death, and significantly
lowers ashy storm-petrel breeding
success on Southeast Farallon Island
(CBD 2007, p. 31). This claim is not
supported by the information contained
in Ainley et al. (1990, pp. 128-163).
Specifically, out of a total of 274 ashy
storm-petrel eggs laid during 1972-83,
Ainley et al. (1990, p. 156) inferred
predation by feral house mice of one
ashy storm-petrel chick, based upon the
remains of a partially eaten carcass.
Twenty-six eggs (9.5 percent) were
categorized as failed to hatch, 9 eggs (3.3
percent) were abandoned, 8 eggs (2.9
percent) ‘‘disappeared,’’ and 2 eggs (0.7
percent) were found broken; however,
house mice were not mentioned as a
significant cause of egg failure.
Furthermore, our review of the available
information reveals no information that
suggests nonnative house mice pose a
significant direct predation threat to
ashy storm-petrels on Southeast
Farallon Island. We have no data
indicating that house mice prey upon
ashy storm-petrel eggs or chicks
anywhere else within the species’ range.
Channel Islands – Black Rats and Feral
Cats
The petitioner claims that nonnative
black rats and feral cats are documented
predators of seabird eggs, chicks, and
adults; that black rats are extant on San
Miguel, Santa Catalina, and San
Clemente Islands; and feral cats may
still impact ashy storm-petrel
populations on Santa Catalina and San
Clemente Islands (CBD 2007, p. 32).
Beyond these claims, the petitioner
provides no specific information
documenting predation of ashy stormpetrels by nonnative black rats or feral
cats.
Nonnative black rats and (feral) cats
are well-documented predators of
seabird eggs, chicks, and adults and
have caused seabird population declines
worldwide, including California
(McChesney and Tershey 1999, pp. 335347; Jones et al. 2008, pp. 16-26). At San
Miguel Island proper, black rats have a
limited distribution, primarily found in
shoreline and bluff habitats on the west
and north sides of the island (Erickson
and Halvorson 1990, p. 13). Possible
nesting of ashy storm-petrels on San
Miguel Island proper has been
presumed, based on birds with brood
patches captured in mist nets deployed
between Harris Point and Cuyler Harbor
(on the island’s north side) (Carter et al.
2008, p. 119). Ashy storm-petrels may
also breed in cliffs near Hoffman Point,
on San Miguel Island proper (Carter et
al. 2008c, p. 17). However, no
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population estimate for ashy stormpetrels is available for San Miguel
Island proper (Carter et al. 1992, p. I-87).
As stated earlier, the black rat is a
potential nonnative predator of ashy
storm-petrels (McChesney and Tershey
1998, p. 342), although predation of
ashy storm-petrels by rats has not been
documented. Predation of ashy stormpetrels at Santa Catalina Island and San
Clemente Island by feral cats has not
been documented. Ashy storm-petrels
have been confirmed to nest in very
small numbers (approximately 0.2
percent of total breeding population) on
offshore rocks at Santa Catalina Island
(Ship Rock) and San Clemente Island
(Seal Cove Area), locations that are
likely inaccessible to feral cats on the
islands proper. Therefore, we conclude
that it is likely that less than one
percent of the total population of ashy
storm-petrels may be susceptible to
predation from black rats and feral cats.
We have examined the available
information concerning the predation
threat from nonnative black rats and
feral cats and have found no direct
evidence showing that black rats and
cats currently prey on ashy stormpetrels in the Channel Islands,
Southeast Farallon Island, or rangewide.
Santa Cruz Island – Barn Owl
The petitioner includes the barn owl
on its list of native avian predators of
ashy storm-petrels but provides no
further information regarding this threat
(CBD 2007, p. 30). Barn owls have a
worldwide distribution and occur
throughout the range of the ashy stormpetrel (Marti 1992, p. 1; Rudolph 1970,
p. 8). Barn owls hunt mostly at night but
occasionally diurnally (Marti 1992, p.
3). Most hunting is done in low flight
above ground in open habitats (Bunn et
al. 1982, p. 11), but some hunting
occurs from perches (Taylor 1994, p.
58). McIver (2002, p. 46) reports that
nest-site searching behaviors of adult
ashy storm-petrel adults and the
mobility of older chicks are activities
that increase the susceptibility of ashy
storm-petrels to predation by barn owls.
At Santa Cruz Island, researchers have
observed predation of ashy stormpetrels by barn owls. In a study at five
breeding locations on Santa Cruz Island,
McIver (2002, p. 69) documented 83
ashy storm-petrels (76 adults and 7
chicks) killed by barn owls from 1995 to
1997. Approximately 97.6 percent of
these ashy storm-petrels were at two
locations (75 birds at Bat Cave and 6
birds at Orizaba Rock) (McIver 2002, p.
69). More recent data reported that 13
ashy storm-petrels were killed by barn
owls on Santa Cruz Island from 2005 to
2008 (McIver and Carter 2006, pp. 3-4;
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McIver et al. 2008, pp. 4-6; McIver et al.
2009, pp. 5-10). At Santa Cruz Island,
the mortality rate of ashy storm-petrel
adults due to barn owl predation was
approximately 5.4 percent during the
1995-97 period (n = 350 estimated
number of adults in nests) and 0.8
percent during the 2005 to 2008 period
(n = 304 estimated number of adults in
nests) (McIver and Carter, unpublished
data). Our analysis indicates that
mortality of ashy storm-petrels due to
barn owls was heavy during the 1995 to
1997 period (McIver 2002, p. 30), but is
currently much reduced (McIver et al.,
in preparation, p. 1); the reason for this
decline is unknown. We conclude that
reduced avian predation on Santa Cruz
Island is the most likely explanation for
the observed increase in ashy stormpetrel productivity (for ashy stormpetrels that have escaped skunk
predation) there. In addition, we
conclude that current levels of
predation of ashy storm-petrels by barn
owls at Santa Cruz Island do not
constitute a substantial threat to the
species. Since barn owls do not occur
anywhere else within the range of the
ashy storm-petrel, we also conclude that
barn owls are not a threat to the ashy
storm-petrel rangewide.
Santa Cruz Island – Island Spotted
Skunk
Ashy storm-petrels are known to
breed at 11 locations on Santa Cruz
Island (Carter et al. 2008, p. 119), and
for this status review, we have compiled
information from many sources to
estimate the number of ashy stormpetrels breeding in sea caves and on
offshore rocks at Santa Cruz Island.
Ashy storm-petrels may nest in crevices
that occur in steep cliffs on Santa Cruz
Island (Carter et al. 2008, p. 121);
however, accessing and censusing these
cliffs is extremely difficult for
researchers, and, therefore, we can
provide no estimate here of numbers of
ashy storm-petrels that may nest in cliffs
at Santa Cruz Island. Excluding Orizaba
(‘‘Sppit’’) Rock, Carter et al. (1992, p. I87) estimated 273 breeding ashy stormpetrels during the periods from 1975 to
1980 and 1989 to 1991 at offshore rocks
at Santa Cruz Island, based on
summaries of historical data and mark–
recapture data. Based on a total of
average numbers of active nests
observed at each location (McIver and
Carter 2006, pp. 2-3; Carter et al. 2007,
pp. 7-9; McIver et al. 2008, pp. 4-6;
McIver et al. 2009, p. 24) and other
information (Carter et al. 1992, p. I-87;
McIver et al. 2009, p. 24; Carter,
unpublished data; McIver et al. in
preparation), approximately 32 breeding
ashy storm-petrels utilized Orizaba
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Rock, and 231 breeding ashy stormpetrels utilized sea caves at Santa Cruz
Island during 2005 to 2008. Combining
these population values, we estimate
that 305 ashy storm-petrels nested on
offshore rocks at Santa Cruz Island, and
230 ashy storm-petrels nested in sea
caves at Santa Cruz Island from 2005 to
2008. Therefore, approximately 43
percent of ashy storm-petrels nesting at
Santa Cruz Island used sea caves from
2005 to 2008. This translates to
approximately 7 to 9 percent of the total
ashy storm-petrel population,
depending on the population estimates
used.
The island spotted skunk occurs only
on Santa Rosa and Santa Cruz Islands
(Crooks and Van Vuren, p. 380) and
constitutes no threat to ashy stormpetrels anywhere else. On Santa Cruz
Island, the island spotted skunk
population has increased recently from
rare to abundant (Crooks and Van Vuren
1994, p. 380; Jones, et al. 2008, p. 76).
Jones et al. (2008, pp. 81-84) reports that
there are two explanations for this
increase in spotted skunk numbers at
Santa Cruz Island: competitive release
(an increase in population due to
reduced competition) due to decline of
the island fox (Urocyon littoralis
santacruzae), and recovery of vegetation
due to removal of feral livestock. In a
radio-telemetry study on Santa Cruz
Island, Crooks and Van Vuren (1994, pp.
381-382) found that island spotted
skunks utilized chaparral grasslands,
open grasslands, and coastal sage scrub
habitats; fed on deer mice, lizards, and
insects; and were active only at night.
Jones et al. (2008, p. 80) reported that
island spotted skunks also utilized
fennel-dominated and riparian habitats.
Like other sea caves in which ashy
storm-petrels nest at Santa Cruz Island,
Bat Cave and Cavern Point Cove Caves
occur at the base of sheer cliffs and
coastal bluffs (McIver 2002, p. 8). The
coastal slopes above the sea caves at
Santa Cruz Island comprise coastal bluff
scrub habitat (Junak et al. 1995, p. 14),
likely utilized by island spotted skunks.
Skunks may have fallen or jumped off
nearby bluffs or cliffs and swam into the
caves (Carter and McIver 2006, p. 4).
Like other procellariids, ashy stormpetrels have a strong and distinctive
musky odor (James-Veitch 1970, p. 86),
and this odor can be detected at the
entrances of the sea caves at Santa Cruz
Island in which ashy storm-petrels nest
(McIver, personal observation). In
addition, ashy storm-petrels return to
and depart their nesting colonies at
night, and nighttime activities at nesting
locations include vocalizations and
aerial displays, including circling flights
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at the sea cave entrances (James-Veitch
1970, p. 24; McIver personal
observation).
During the period from 2005 to 2008,
researchers reported that island spotted
skunks killed at least 100 ashy stormpetrels at two locations on the northeast
coast of Santa Cruz Island: 70 ashy
storm-petrels at Bat Cave in 2005 and 32
ashy storm-petrels at Cavern Point Cove
Caves in 2008 (McIver and Carter 2006,
p. 3; McIver et al. 2009, p. 7). The
mortality event at Bat Cave in 2005
resulted in the temporary loss of the
largest ashy storm-petrel colony at Santa
Cruz Island (average of 80 nests per year
in 1995-97 (McIver 2002, p. 24)) and the
colony with the largest numbers of
monitored nests of the ashy storm-petrel
(McIver and Carter 2006, p. 4). One
skunk was live-trapped and removed
from the cave in June 2005, and the
other was presumed to have died in or
left the cave by the next year (McIver
and Carter 2006, p. 3; Carter et al. 2007,
p. 7). Ashy storm-petrel nests were
documented in Bat Cave in 2006 (19
nests), 2007 (28 nests), and 2008 (40
nests), and no further evidence of
skunks in the cave has been observed
since 2005 (Carter et al. 2007, p. 7;
McIver et al. 2008, p. 4; McIver et al.
2009, p. 6). The mortality event at
Cavern Point Cove Caves in 2008,
located approximately 0.6 mi (1 km)
east of Bat Cave, resulted in the death
of at least 32 adult ashy storm-petrels
and complete reproductive failure at
this location in 2008 (McIver et al. 2009,
p. 7). A skunk was live-trapped and
removed from Cavern Point Cove Caves
in early July 2008, and marked and
released on the island approximately 2.5
mi (4 km) southeast from the capture
location (McIver et al. 2009, p. 7). Livetraps were deployed in Bat Cave and
Cavern Point Cove Caves and monitored
regularly for the remainder of the 2008
breeding season, to capture and remove
skunks and prevent further storm-petrel
deaths (McIver et al. 2009, p. 7). A
second spotted skunk was caught in a
live trap at Cavern Point Cove Caves in
September 2008, but died. After the
2005 predation event at Bat Cave,
researchers considered the skunkpredation incident to be an isolated,
unusual event (McIver and Carter 2006,
p. 4). Recent research shows that island
spotted skunk population numbers at
Santa Cruz Island have likely increased
to carrying capacity, possibly in
response to reduced numbers of island
foxes (Jones et al. 2008, pp. 81-84).
Given the additional skunk-predation
incident in 2008, and known increases
in island spotted skunk population
numbers on the island, ashy storm-
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petrels nesting in sea caves on Santa
Cruz Island may be vulnerable to
episodic predation by skunks (McIver et
al. 2009, p. 14). The spotted skunk diet
is largely comprised of invertebrates and
vertebrates other than birds. For
example, during 1992, occurrence of
avian remains in spotted skunk scat
occurred only in 4 percent of acquired
samples. Samples in 2003 and 2004
contained no avian remains (Jones et al.
2008, pp. 81-84).
The future of island spotted skunk
population numbers and trends at Santa
Cruz Island is uncertain and may be
directly related to the recovery status of
the island fox (Jones et al. 2008, p. 83).
A recovering population of island foxes
may or may not be able to suppress the
population of island spotted skunks to
its former levels, and this may result in
a new equilibrium of fox and skunk
population numbers at Santa Cruz
Island (Jones et al. 2008, p. 83).
Regardless, spotted skunk predation is
unlikely to increase beyond levels
observed in recent years, because Jones
et al. (2008, p. 83) suggested that skunks
may have been approaching or even
exceeding carrying capacity during their
study. The conclusion of Jones et al.
(2008, p. 83) was supported by a trend
toward smaller skunk body size and
undiminished skunk home ranges in
2003–2004 versus 1992. In addition, the
proportion of juvenile skunks captured
decreased during the study, from 24
percent in September 2003 to 5 percent
in September 2004. This leads us to
believe that the spotted skunk predation
will not likely affect more than a very
small percentage (approximately 7 to 9
percent) of the overall ashy storm-petrel
population.
Santa Cruz Island is owned and
managed by the Park and the Nature
Conservancy. The Park owns and
manages approximately the eastern 25
percent of the island, where two ashy
storm-petrel sea-cave locations (Bat
Cave and Cavern Point Cove Caves)
occur; the Park also manages the
offshore rocks at the island, six of which
(Del Mar Rock, Diablo Rocks, Orizaba
Rock, Scorpion Rock, Willow
Anchorage Rocks, and Gull Island) are
ashy storm-petrel breeding locations.
The Nature Conservancy owns
approximately the western 75 percent of
the island, where three ashy stormpetrel sea caves (Shipwreck Cave, Dry
Sandy Beach Cave, and Cave of the
Bird’s Eggs) occur. Currently,
monitoring of nesting success of ashy
storm-petrels at Santa Cruz Island is
being conducted in association with
restoration activities, funded through
2010 by the Montrose Settlements
Restoration Program (Montrose
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Settlements Restoration Program 2005,
p. 196). Researchers have proposed the
development and implementation of a
skunk management plan to prevent
skunk predation of storm-petrels in sea
caves at Santa Cruz Island; this plan is
scheduled to be implemented by the
Park during 2009-10 (McIver et al. 2009,
p. 16).
Further research on population size,
trends, and distribution of island
spotted skunks at Santa Cruz Island is
needed. Based on the relatively isolated
mortality events at Bat Cave and Cavern
Point Cove Caves, we characterize the
threat of predation by island spotted
skunks as sporadic and believe that
efforts to control skunks by the Park will
diminish the possibility of skunk
predation even further. We estimate that
approximately 7 to 9 percent of the total
population of ashy storm-petrels is
susceptible to this episodic threat, and
therefore predation by island spotted
skunks is not a significant concern at
the Channel Islands, nor is it a threat in
any way at Southeast Farallon Island, or
rangewide.
Santa Cruz Island – Deer Mice
Deer mice occur in a variety of
habitats on Santa Cruz Island, including
chaparral, rocky outcrops, marsh,
riparian, pine forest, oak woodland,
buildings, and sea caves (Mayfield et al.
2000, pp. 509; McIver 2002, pp. 29-30).
Egg predation by deer mice has been
documented for crevice-nesting seabird
species and usually occurs during
periods of parental absence (Murray et
al. 1983, p. 17; Drever et al. 2000, pp.
2013-2015; Blight et al. 1999, pp. 872873). In a 4–year study at Santa Cruz
Island, McIver (2002, pp. 40-41)
reported that deer mice scavenged or
preyed upon at least four ashy stormpetrel eggs, and concluded that egg
predation by deer mice was likely not a
major cause of egg mortality there. In
addition, (McIver 2002, p. 41) reported
that two ashy storm-petrel chicks were
found partially eaten by mice, although
it was unknown if mice killed these
chicks or scavenged them after they had
died of other causes. Similarly,
researchers at Santa Cruz Island during
2005 to 2008 did not find predation of
ashy storm-petrel eggs by deer mice to
be significant (less than six total)
(McIver and Carter 2006, pp. 2-4; Carter
et al. 2007, pp. 8-24; McIver et al. 2008,
p. 5; McIver et al. 2009, pp. 5-8). Our
review of the available information
reveals no other information that
indicates predation of ashy storm-petrel
eggs by deer mice is a substantial threat
at the Channel Islands, Southeast
Farallon Island, or rangewide.
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Disease
The petitioner did not raise disease as
a threat to the ashy storm-petrel.
Moreover, disease in ashy storm-petrels
has not been reported as a threat to the
species (Ainley 1995, p. 8). Accordingly,
we conclude disease is not a threat to
the ashy storm-petrel on Southeast
Farallon Island, the Channel Islands, or
rangewide.
Summary of Factor C
Approximately 36 to 53 percent of all
ashy storm-petrels breed on Southeast
Farallon Island, and ashy storm-petrels
are preyed upon by several predator
species, the most notable being western
gulls. Avian predation of ashy stormpetrels has persisted on Southeast
Farallon Island at similar or increasing
levels since at least 1994, yet recent
reports show that ashy storm-petrel
survival appears to be increasing, and
their total numbers also appear to be
increasing. Therefore, at this time, we
do not consider predation by western
gulls to be a significant threat to ashy
storm-petrels. Our analysis of the
available information reveals little
information regarding the extent of
burrowing owl predation, and predation
of ashy storm-petrel eggs and chicks by
nonnative house mice on Southeast
Farallon Island does not pose a
significant threat to ashy storm-petrels.
We conclude that predation of ashy
storm-petrels by island spotted skunks
on Santa Cruz Island could occur on a
sporadic basis, but thus far, spotted
skunks have affected less than 7 to 9
percent of the total ashy storm-petrel
population. Once removed, spotted
skunks no longer pose a threat to ashy
storm-petrels, and monitoring for
skunks is planned in coming years. We
conclude that predation of ashy stormpetrel adults and chicks by barn owls,
and predation of ashy storm-petrel eggs
by deer mice on Santa Cruz Island do
not pose a threat to ashy storm-petrels.
Finally, we conclude that predation of
ashy storm-petrels by feral cats and
nonnative black rats does not pose a
significant threat to ashy storm-petrels.
Factor D: Inadequacy of Existing
Regulatory Mechanisms
The petitioner asserts that existing
regulatory mechanisms have been
ineffective at preventing the decline of
the ashy storm-petrel and in mitigating
many of the threats to the species (CBD
2007, p. 32). The petitioner claims that
the ineffectiveness of regulatory
mechanisms is demonstrated by the
failure to eradicate nonnative predators,
the inadequate regulation of artificial
light pollution, the failure to restrict
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human disturbance at breeding sites, the
lack of regulations on greenhouse gases,
and the failure of the Migratory Bird
Treaty Act (16 U.S.C. 703-712) to protect
the species from the identified threats
(CBD 2007, pp. 32-35). Consequently, in
this section we discuss these and other
regulatory mechanisms.
U.S. Federal Protection
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National Environmental Policy Act
The National Environmental Policy
Act of 1970 (NEPA) (42 U.S.C. 4371 et
seq.) requires that all activities
undertaken, authorized, or funded by
Federal agencies be analyzed for
potential impacts to the human
environment prior to implementation.
NEPA does not require adverse impacts
be fully mitigated, and some impacts
could still occur. Additionally, NEPA is
only required for projects with a Federal
nexus, and therefore, actions that do not
require a Federal permit or occur on
private land are not required to comply
with this law.
Migratory Bird Treaty Act
The Migratory Bird Treaty Act of 1918
(MBTA) states that it is unlawful ‘‘to
pursue, hunt, take, capture kill, or
attempt to take, capture or kill, possess,
offer for sale, sell, offer to barter, barter,
offer to purchase, purchase, deliver for
shipment, ship, export, import, cause to
be shipped, exported, or imported,
deliver for transportation, transport or
cause to be transported, carry or cause
to be carried, or receive for shipment,
transportation, carriage, or export, any
migratory bird, any part, nest, or eggs of
any such bird, or any product, whether
or not manufactured.’’ The ashy stormpetrel is included in the list of migratory
birds protected by the MBTA. The
MBTA provides penalties for anyone in
violation of its provisions. The
petitioner claims that the MBTA does
not provide protection from many of the
threats facing the species such as plastic
pollution, light pollution, nonnative
predators, and changing ocean
conditions as a consequence of global
warming (CBD 2007, p. 36). In addition,
the petitioner asserts that, unlike the
Act, the MBTA provides no citizen suit
provision, no requirement for
designation or protection of critical
habitat, no consultation provision to
ensure Federal agency actions do not
jeopardize the species, nor an
affirmative conservation mandate to
recover the species. The provisions of
the MBTA prevent hunting, capturing,
or killing or attempting to take, capture,
or kill, or possess ashy storm-petrels.
The degree to which the protections are
applied are a matter of enforcement and
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there are likely to be instances where
permits under the MBTA are not
obtained and some mortality may occur.
However, our analysis did not reveal
information that would suggest a level
of mortality that would be a significant
threat to the species. Overall the MBTA
provides protections for the ashy stormpetrel that would otherwise not exist.
On January 10, 2001, President
Clinton issued Executive Order 13186,
pertaining to responsibilities of Federal
agencies to protect migratory birds, and
directing executive departments and
agencies to further implement the
MBTA (66 FR 3853; January 17, 2001).
Executive Order 13186 directs each
Federal agency taking actions that have,
or are likely to have, a measurable
negative effect on migratory bird
populations to develop and implement
(within 2 years) a memorandum of
understanding (MOU) with the Service
that promotes the conservation of
migratory bird populations. The DOD
entered into a MOU with the Service on
August 30, 2006 (71 FR 51580), which
emphasizes a general collaborative
approach to conservation of migratory
birds. Conservation measures include
minimizing disturbance to breeding,
migration, and wintering habitats. While
this MOU is non-binding and it does not
authorize the take of migratory birds, it
does provide an additional opportunity
for the Service to continue to reduce the
threat of habitat loss to the ashy stormpetrel on lands owned and managed by
the DOD, including San Clemente
Island. Currently, approximately 0.1
percent of the entire ashy storm-petrel
population breeds on DOD lands. We
are not aware that any other Federal
agency has entered into a similar MOU
with the Service.
National Wildlife Refuge System
Improvement Act of 1997
The National Wildlife Refuge System
is managed by the Service primarily for
the benefit of fish, wildlife, and plant
resources and their habitats (Service
2008, p. 2). The Farallon National
Wildlife Refuge (Refuge) was
established in 1909, is located
approximately 28 miles west of San
Francisco, and is composed of several
islands, including Southeast Farallon
Island. On December 22, 2008, we
published a notice in the Federal
Register announcing the availability of
a draft Comprehensive Conservation
Plan (CCP) and environmental
assessment to manage natural resources
at the Refuge (73 FR 78386). As stated
earlier, ashy storm-petrels at Southeast
Farallon Island are susceptible to
predation by western gulls (which breed
at the island) and burrowing owls
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(which do not breed at the island but are
regular fall migrants and overwinter at
the island). Managers at the Refuge are
concerned about high levels of avian
predation upon and reduced
productivity and survivorship of ashy
storm-petrels at Southeast Farallon
Island. Consequently, within 5 years of
approval of the final CCP (anticipated in
year 2010), the Refuge proposes the
following management actions: (1)
Develop a plan to eradicate the
nonnative house mouse through
rodenticide application and prevent
future human introductions of mice; (2)
translocate to the mainland individual
burrowing owls that overwinter on
Southeast Farallon Island, until mice at
the island are eradicated; (3) monitor
western gull nests for ashy storm-petrel
remains, and conduct experimental
selective removal (culling) of no more
than 10 western gulls annually to
reduce predation upon ashy stormpetrels; and (4) monitor the ashy stormpetrel population (Service 2008, pp. 84,
98).
The management actions, once
implemented, may be successful in
reducing predation of ashy storm-petrels
by western gulls and burrowing owls,
which, in turn, may result in an increase
in productivity and survivorship of ashy
storm-petrels at Southeast Farallon
Island. However, we are not basing our
finding of whether listing is warranted
on future actions contained in the draft
CCP. Nevertheless, the proposed
management actions in the Refuge’s
draft CCP, when approved and funded,
will likely benefit the ashy storm-petrel
at Southeast Farallon Island, where an
estimated 36 to 53 percent of all
breeding ashy storm-petrels occur.
National Park Service Organic Act
The National Park Service Organic
Act (16 U.S.C. l et seq.) established the
U.S. National Park Service, ‘‘* * * to
promote and regulate the use of the * *
* national parks * * * which purpose is
to conserve the scenery and the natural
and historic objects and the wild life
therein and to provide for the enjoyment
of the same in such manner and by such
means as will leave them unimpaired
for the enjoyment of future
generations.’’ On March 5, 1980, the
U.S. Congress established as the
Channel Islands National Park (Park) the
islands of San Miguel, Santa Rosa, Santa
Cruz, Anacapa, Santa Barbara, and the
submerged lands and waters within one
nautical mile of each island. In 2007, in
accordance with 36 CFR, Chapters 1-7,
the Park prohibited access by park
visitors on: 1) Offshore rocks and islets
in the Park; 2) Bat Cave and Cavern
Point Cove Caves, Santa Cruz Island;
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and 3) shorelines and cliffs at Santa
Barbara Island, to protect wildlife and
natural resources, including ashy stormpetrels (NPS 2007, p. 2). Thus, visitor
access is prohibited at 16 ashy stormpetrel breeding locations (locations #722, in Table 1) managed by the National
Park Service, which constitutes
approximately 99 percent of the
breeding locations in the Channel
Islands and, depending on population
estimates, approximately 44 to 60
percent of the ashy storm-petrel
breeding locations rangewide.
Under the authority of the Antiquities
Act of 1906, the California Coastal
National Monument (CCNM) was
established by Presidential
Proclamation number 7264, on January
11, 2000. The Presidential Proclamation
defined the CCNM as all unappropriated
or unreserved lands and interest in
lands owned or controlled by the United
States in the form of islands, rocks,
exposed reefs, and pinnacles above
mean high tide within 12 nautical miles
of the shoreline of the State of
California. The CCNM is comprised of
more than 20,000 small islands, rocks,
exposed reefs, and pinnacles within the
corridor extending 12 nautical miles
(22.2 km) from the shoreline between
Mexico and Oregon. This proclamation
directed the Secretary of the Interior to
manage the monument through the
Bureau of Land Management (BLM). In
2005, the BLM approved a resource
management plan for the CCNM (BLM
2005), which contains broad direction
for the protection of the geologic
formations and habitats for seabirds,
and focuses on multi-agency and other
partnerships and involvement of local
communities as the keys to management
and protection. Five ashy storm-petrel
breeding locations (locations # 1, 2, 6,
23 and 24 in Table 1) are managed by
the BLM, which, depending on
population estimates used, comprise
about 1.2 percent to 1.7 percent of the
total population of breeding ashy stormpetrels.
Sikes Act
The Sikes Act of 1960 (16 U.S.C. 670
et seq.) authorizes the Secretary of
Defense to develop cooperative plans for
conservation and rehabilitation
programs on military reservations and to
establish outdoor recreation facilities,
and provides for the Secretaries of
Agriculture and the Interior to develop
cooperative plans for conservation and
rehabilitation programs on public lands
under their jurisdiction. The Sikes Act
Improvement Act of 1997 required
Department of Defense (DOD)
installations to prepare Integrated
Natural Resources Management Plans
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(INRMPs). Consistent with the use of
military installations to ensure the
readiness of the Armed Forces, INRMPs
provide for the conservation and
rehabilitation of natural resources on
military lands and incorporate, to the
maximum extent practicable, ecosystem
management principles and provide the
landscape necessary to sustain military
land uses. The U.S. Navy currently
controls feral cats on San Clemente
Island through an existing INRMP
(Hering 2008, p. 6), and this may benefit
the small numbers of ashy storm-petrels
nesting there.
National Marine Sanctuaries Act
The National Marine Sanctuaries Act
of 1972 (NMSA) (16 U.S.C. 1431 et seq.)
authorizes the Secretary of Commerce,
and specifically the National Oceanic
and Atmospheric Administration
(NOAA), to designate and protect areas
of the marine environment with special
national significance due to their
conservation, recreational, ecological,
historical, scientific, cultural,
archeological, educational, or esthetic
qualities as national marine sanctuaries.
Within the range of the ashy stormpetrel, the four national marine
sanctuaries (NMS) that have been
designated in California are: the
Channel Islands NM Sanctuary (CINMS)
off the coast of southern California
(1980); Gulf of the Farallons NMS
(formerly Point-Reyes Farallon Islands
NMS [1981]); Cordell Bank NMS off the
coast of central California (1989); and
the Monterey Bay NMS (1992). In 1989,
Congress passed a law that prohibits the
exploration for, or the development or
production of, oil, gas, or minerals in
any area of the Cordell Bank National
Marine Sanctuary (P.L. 101-74). The
Oceans Act of 1992 (P.L. 102-587)
prohibits leasing, exploration of,
producing, or developing oil and gas in
the Monterey Bay National Marine
Sanctuary; and includes a requirement
for Federal agencies to consult with the
program on activities that are likely to
injure sanctuary resources. In 2007,
NOAA expanded the state ‘‘no-take’’
marine reserves and one of the limited
take marine conservation areas in the
CINMS to include Federal waters out to
6 nautical miles (11 km), which
prohibited or limited removal of, and
injury to, any CINMS resource,
including ashy storm-petrels (NOAA
2007, pp. 29208-29235). Specifically,
lobster harvest and recreational fishing
for pelagic finfish (with hook and line
only) are allowed within the marine
conservation area, while all other
extraction or injury to CINMS resources
is prohibited (NOAA 2007, p. 29212).
These Federal marine reserves were
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established in conjunction with State of
California regulatory processes (see
‘‘State of California Protection’’
subsection below). In addition, on
March 25, 2005, the California Fish and
Game Commission adopted the Market
Squid Fishery Management Plan
(MSFMP; California Fish and Game
Commission 2005, pp. 1-558), which
prohibits taking of market squid using
attracting lights in all waters of the Gulf
of the Farallons NMS at any time.
Accordingly, there are regulatory
measures that prohibit the use of bright
lights for commercial fishing at 10 ashy
storm-petrel breeding locations,
including around Southeast Farallon
Island, which constitute approximately
36 to 53 percent of the rangewide
population and for approximately 16
percent of the remainder of the
population rangewide, for a total of
approximately 52 to 69 percent of the
total population.
Outer Continental Shelf Lands Act
The Outer Continental Shelf Lands
Act of 1953 (OCSLA) (43 U.S.C. 1331 et
seq.) provides the Secretary of the
Interior, on behalf of the Federal
Government, with authority to manage
the mineral resources, including oil and
gas, on the outer continental shelf (OCS)
and defines the OCS as all submerged
lands lying seaward of the State and
Federal boundary. The Federal Oil &
Gas Royalty Management Act of 1982
(30 U.S.C. 1701 et seq.) mandates
protection of the environment and
conservation of Federal lands in the
course of building oil and gas facilities.
The Secretary of the Interior designated
the Minerals Management Service
(MMS) as the administrative agency
responsible for the mineral leasing of
submerged OCS lands and for the
supervision of offshore operations after
lease issuance. In managing the offshore
oil and gas resources, the MMS
conducts environmental studies, issues
leases, and regulates operations
conducted on the OCS. The regulatory
responsibilities include issuing permits
for oil and gas exploration,
development, and production and
inspecting operations during all of these
activities. Within the range of the ashy
storm-petrel, the MMS manages the
offshore mineral resources of 23 active
leases and 36 undeveloped leases, in
coordination with other Federal, State,
and local agencies and in consultation
with the public (McCrary et al. 2003, pp.
43-45).
Deepwater Port Act of 1974
The Deepwater Port Act of 1974
(DWPA) (33 U.S.C. 1501 et seq.)
authorizes the U.S. Coast Guard (USCG;
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Department of Homeland Security) to
regulate Liqufied Natural Gas deepwater
ports and shoreside terminals.
Originally pertaining only to oil, the
Maritime Transportation Security Act of
2002 (MTSA) (33 U.S.C. 1221 et seq.)
amended the DWPA to include natural
gas. The regulations pertaining to the
licensing, design, equipment and
operation of deepwater ports and
shoreside terminals are found in Title
33 CFR parts 148, 149 and 150. The
Secretary of the Department of
Homeland Security delegated the
processing of DWP applications to the
USCG and the Maritime Administration
(MARAD), respectively. MARAD is the
license issuing authority and works in
concert with the USCG in developing
the Environmental Impact Statement,
while the USCG has primary
jurisdiction over design, equipment and
operations and security requirements.
The DWPA established a specific time
frame of 330 days from the date of
publication of a Federal Register notice
of a ‘‘complete’’ application to the date
of approval or denial of a deepwater
port license. Among other requirements,
an applicant for a deepwater port
license must demonstrate consistency
with the Coastal Zone Management Plan
of the adjacent coastal States. The USCG
and MARAD, in cooperation with other
Federal agencies, must comply with the
requirements of the National
Environmental Policy Act in processing
deepwater port applications within the
timeframes prescribed in the DWPA. To
date the USCG has received the
following two deepwater port
applications, which are pending USCG
approval, and occur within the range of
the ashy storm-petrel: Clearwater Port
LNG, Project NorthernStar Natural Gas;
and Port Esperanza, Esperanza Energy
LLC. A third proposed LNG project, the
Oceanway LNG Terminal, was
withdrawn by Woodside Petroleum,
Ltd. in January 2009 (Woodside
Petroleum Ltd. 2009, pp. 1-2).
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Federal Power Act of 1920
Section 23(b)(1) of the Federal Power
Act of 1920 (16 U.S.C. 791a et. seq.)
grants jurisdiction to the Federal Energy
Regulatory Commission (FERC) for the
licensing of hydropower development
(for example, wave energy projects) in
offshore waters of the United States. We
are aware of at least one proposed wave
energy project that occurs within the
range of the ashy storm-petrel. FERC
licensing procedures include analyzing
potential project effects on natural
resources including, but not limited to,
water quality, water use, marine
mammals, fish, birds, geology, land use,
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ocean use, navigation, recreation,
aesthetics, and cultural resources.
Oil Pollution Act of 1990 (OPA)
The Oil Pollution Act of 1990 (33
U.S.C. 2701 et. seq.) amended the Clean
Water Act and addressed the wide range
of problems associated with preventing,
responding to, and paying for oil
pollution incidents in navigable waters
of the United States. It created a
comprehensive prevention, response,
liability, and compensation regime to
deal with vessel- and facility-caused oil
pollution to U.S. navigable waters. The
OPA increased Federal oversight of
maritime oil transportation and
provided environmental safeguards by:
setting new requirements for vessel
construction and crew licensing and
manning; mandating contingency
planning; enhancing Federal response
capability; broadening enforcement
authority; increasing penalties and
potential liabilities; and creating new
research and development programs.
Various Federal agencies are responsible
for implementing the OPA. The
Environmental Protection Agency (EPA)
is responsible for non-transportationrelated onshore facilities and incidents
in the Inland Zone, the USCG is
responsible for marine transportationrelated facilities and incidents in the
Coastal Zone, MARAD (in the
Department of Transportation) is
responsible for promoting the U.S.
merchant marine and shipbuilding
industry, and the Department of
Commerce (specifically, NOAA) is
responsible for natural resource damage
assessments relating to oil discharges.
The OPA requires a phase-out of singlehull tankers from U.S. waters by 2015.
Committee on Oil Pollution Act of 1990
et al. (1998, p. 147) report that although
the mandatory phase-out schedule of
section 4115 of the OPA bans all singlehull tankers (without double bottoms or
double sides) from U.S. trade after 2010,
it is probable that under the deepwater
port and lightering zone exemption,
large single-hull vessels up to 30 years
of age will operate in the United States
through 2015. For this status review, we
could not find specific information
indicating how many single-hull tankers
currently utilize California waters, and
whether compliance with the doublehull provisions of section 4115 of the
OPA will be achieved. The OPA
imposes liability for removal costs and
damages resulting from an incident in
which oil is discharged into navigable
waters or adjoining shorelines or the
exclusive economic zone. In 2006, a
damage assessment, restoration plan,
and environmental assessment
(Luckenbach 2006, pp. 1-165) was
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presented by Natural Resource Trustee
Agencies (Service, NOAA, National Park
Service, and California Department of
Fish and Game) for natural resources
(including ashy storm-petrels) injured
during multiple oil spills that occurred
off the coast of San Francisco,
California, from 1990 to December 2003.
Clean Air Act of 1970
The Clean Air Act of 1970 (42 U.S.C.
7401 et seq.) EPA to develop and
enforce regulations to protect the
general public from exposure to
airborne contaminants that are known to
be hazardous to human health. In 2007,
the Supreme Court ruled that gases that
cause global warming are pollutants
under the Clean Air Act, and that the
EPA has the authority to regulate carbon
dioxide and other heat-trapping gases
(Massachusetts et al. v. EPA 2007 [Case
No. 05-1120]). The petitioner claims that
the ashy storm-petrel is threatened by a
lack of regulatory mechanisms to curb
greenhouse gases (GHG) that contribute
to global temperature rises, ocean
acidification, and sea level rise (CBD
2007, p. 34). As stated earlier, our status
review did not reveal information that
indicates productivity of ashy stormpetrels is adversely affected by ocean
acidification, and we conclude that sea
level rise within the next 40 to 50 years
is not a significant threat to ashy stormpetrels.
State of California Protection
The California Department of Fish
and Game (CDFG) is the State agency
responsible for managing California’s
fish, wildlife, and plant resources, and
the habitats upon which they depend,
for their ecological values and for their
use and enjoyment by the public. The
ashy storm-petrel is designated as a
Species of Special Concern by the CDFG
(Carter et al. 2008, pp. 117-124). This
status does not confer regulatory
protection to the species and applies to
animals not listed under the Act or the
California Endangered Species Act
(CESA), but which nonetheless (1) are
declining at a rate that could result in
listing, or (2) historically occurred in
low numbers and known threats to their
persistence currently exist. In addition,
this designation is intended to result in
special consideration for these animals
by the CDFG, land managers, consulting
biologists, and others, and is intended
to: focus attention on the species to
achieve conservation and recovery of
these animals before they meet CESA
criteria for listing as threatened or
endangered; stimulate collection of
additional information on the biology,
distribution, and status of poorly known
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at-risk species; and focus research and
management attention on the species.
California Environmental Quality Act
of 1970 (CEQA) does not regulate land
use, but requires all local and State
agencies to avoid or minimize
environmental damage where feasible,
during the course of proposed projects.
CEQA provides protection not only for
State-listed or federally listed species,
but also for any species designated as
species of special concern by the CDFG.
In 1999, the California legislature
approved and the governor signed the
Marine Life Protection Act (MLPA;
Stats.1999, Chapter 1015). The MLPA
requires that the CDFG prepare and
present to the Fish and Game
Commission a master plan that will
guide the adoption and implementation
of a Marine Life Protection Program,
which includes a statewide network of
marine protected areas. In 2003, the
State of California established nine State
Marine Reserves in the California
Channel Islands, which (in part)
prohibit within these reserves market
squid fishery activities that use bright
lights. In 2008, the CDFG published a
revised draft plan for marine protected
areas in California (CDFG 2008a). The
CDFG has organized a MLPA South
Coast Regional Stakeholder Group to reexamine and re-design the Marine
Protected Areas in southern California,
to increase their coherence and
effectiveness at protecting the State’s
marine life, habitat, and ecosystems.
On March 25, 2005, the California
Fish and Game Commission adopted the
MSFMP (California Fish and Game
Commission 2005, pp. 1-558), which: (1)
Limits the wattage of attracting lights
(see Factor E below) to a maximum of
30,000 watts per boat; (2) requires that
attracting lights be shielded to direct the
light downward, or situated such that
the illumination is completely
submerged underwater; and (3) and
prohibits, at any time, the use of
attracting lights for the purpose of
taking of market squid in all waters of
the Gulf of the Farallons NMS, that
encompasses all of the ashy stormpetrels on Southeast Farallon Island and
approximately 36 to 53 percent of the
ashy storm-petrels rangewide.
Mexican Federal Protection
The ashy storm-petrel is currently
listed as threatened under Mexican Law,
NOM-059-ECOL-2001, and is proposed
as endangered under a draft amendment
of this law (SEMARNAT 2008, p. 39).
Pursuant to this law, general criteria are
to be followed in managing Mexican
wildlife, including, but not limited to:
preservation of biodiversity and natural
species habitats; and preservation of
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endemic, threatened, endangered or
specially protected species. These
considerations apply to all of the ashy
storm-petrels found in Mexico, which
constitutes approximately 1 to 2 percent
of the rangewide population. We have
no new information on the adequacy
and effectiveness of ‘‘threatened’’ or
‘‘endangered’’ status for conservation of
ashy storm-petrels in Mexico.
International Agreements
Since the ashy storm-petrel ranges
into Mexico, international agreements
may provide some protections for the
species. The North American Agreement
on Environmental Cooperation
(NAAEC) was negotiated and is being
implemented in parallel to the North
American Free Trade Agreement.
NAAEC requires that each Party (United
States, Mexico, and Canada) ensure that
its laws provide for high levels of
environmental protection. Each Party
agreed to effectively enforce its
environmental laws through appropriate
means, such as the appointment and
training of inspectors, monitoring
compliance, and pursuing the necessary
legal means to seek appropriate
remedies for violations. The
Commission for Environmental
Cooperation (CEC) was created under
the NAAEC and is authorized to
develop joint recommendations on
approaches to environmental
compliance and enforcement.
Summary of Factor D
Based on our analysis of the existing
regulatory mechanisms, we have found
a diverse network of laws and
regulations that provide protections to
the ashy storm-petrel and its habitat and
effectively ameliorate threats rangewide.
Specific to the ashy storm-petrel,
provisions of the MBTA prohibit killing
or possessing of the species. An
overarching protection of breeding and
foraging habitat through Federal
nexuses in regulatory mechanisms, such
as the Outer Continental Shelf Lands
Act, Federal Power Act, Oil Pollution
Control Act, and the Deepwater Port
Act, provide protections to breeding and
foraging habitat. At Southeast Farallon
Island all of the breeding locations are
located on U.S. Fish and Wildlife
Service, National Wildlife Refuge
System lands which are covered under
the National Wildlife Refuge System
Improvement Act of 1997 (16 U.S.C.
668dd-668ee). Additionally, the waters
surrounding Southeast Farallon Island
are within the Gulf of the Farallons
NMS, where there is a prohibition on
the use of attracting lights for market
squid fishing. In the Channel Islands,
approximately 16 percent of the
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breeding habitat is off limits to the use
of attracting lights for market squid
fishing due to the provisions of the
National Marine Sanctuaries Act.
Additionally, some sea caves on Santa
Cruz Island have been closed to human
visitation and the National Park Service
is planning to develop and implement a
island spotted skunk and nonnative
mouse management plan that will
provide additional protections to the
ashy storm-petrel. Approximately 99
percent of the ashy storm-petrel
breeding locations in the Channel
Islands are located on National Park
Service lands, which are covered under
the National Park Service Organic Act.
Regulatory mechanisms under the State
of California, including CEQA, MLPA,
and provisions under MSFMP, provide
additional protections for the ashy
storm-petrel. Based on our review of the
best available scientific information, we
conclude that adequate regulatory
mechanisms are in place to protect the
species and its habitat throughout its
range, within the Channel Islands, and
at Southeast Farallon Island.
Factor E: Other Natural or Manmade
Factors Affecting the Continued
Existence of the Species
The petitioner asserts that artificial
light pollution due to California market
squid fishery boats, and current and
future offshore energy production
platforms, threatens the continued
existence of the ashy storm-petrel (CBD
2007, pp. 15-17). In addition, the
petitioner claims that contamination
from petroleum (from offshore energy
production platforms and ocean-going
vessels), chlorinated hydrocarbons, and
plastics threaten the continued
existence of the ashy storm-petrel (CBD
2007, pp. 18-20).
Artificial Light Pollution at Breeding
Colonies – Market Squid Fishery and
Tuna Aquaculture
The California market squid is found
from central Baja California, Mexico, to
Southeast Alaska (Roper and Sweeney
1984, p. 95-96). In California, a fishery
for market squid consists of two
geographically distinct components: a
central California fishery off Monterey
and a southern California fishery around
the Channel Islands and along the
mainland coast (Pomeroy and
Fitzsimmons 2001, p. 3). The Service is
not aware of the occurrence of market
squid fishery activities at Islas Los
Coronados and Islas Todos Santos,
which are known ashy storm-petrel
breeding locations in Mexico.
Market squid spawn in sandy
substrates near islands and the coast
(California Fish and Game Commission
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2005, p. 37). Harvest involves luring the
squid to the surface with high wattage
lamps, encircling them with purse seine
nets, pumping and using nets to remove
the squid from the water, and finally
storing them in an on-vessel fish hold
(Hastings and MacWilliams 1999, p. iv).
Market squid fishery activities occur
during squid mating and egg-laying:
April through October in central
California, and October through May in
southern California (Pomeroy and
Fitzsimmons 2001, pp. 2-3; California
Fish and Game Commission (2005, p.
37). Market squid fishery activities
coincide with the peak fledging period
(early to mid-October) and pre-egg and
early egg-laying periods of ashy stormpetrels (February through May) (Ainley
1995, p. 5; McIver 2002, p. 17).
According to the MSFMP (2005, p. 3),
squid may not be taken using attracting
lights in all waters of the Gulf of the
Farallones National Marine Sanctuary at
any time; this closure includes
Southeast Farallon Island. In addition,
squid fishery activities are not permitted
within 11 marine reserves and 2 marine
conservation areas in southern
California, which collectively contain
seven ashy storm-petrel breeding
locations. In California, market squid
fishery activities are permitted at 13
ashy storm-petrel breeding locations.
Although we are not aware whether
market squid fishing occurs at ashy
storm-petrel breeding locations in
Mexico, we are aware of aquaculture
activities associated with the harvest of
northern bluefin tuna (Thunnus
orientalis) at Islas Los Coronados and
Islas Todos Santos, Mexico, which use
bright lights to illuminate at-sea tuna
´
pens (Zertuche-Gonzales et al. 2008,
p.14; McIver, personal observation).
Therefore, bright lights associated with
commercial fishing activities (market
squid fishery and tuna aquaculture) are
permitted at 15 locations that
collectively comprise approximately
1,915 breeding ashy storm-petrels,
which is approximately 25 percent to 34
percent of all breeding ashy stormpetrels, depending on population
estimates used.
Evidence from several studies,
anecdotal observations, and museum
specimens indicate that ashy stormpetrels and related species are attracted
to lights, which puts them at risk for
light-induced mortality (Reed et al.
1985, pp. 377-383; Le Corre et al. 2002,
pp. 93-102). In their study of four
species of procellariids (specifically,
Barau’s petrel (Pterodroma baraui),
Mascarene petrel (Pseudobulweria
aterrima), Audubon’s shearwater
(Puffinus lherminieri bailloni), and
wedge-tailed shearwater (Puffinus
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´
pacificus)) on Reunion Island in the
Indian Ocean, Le Corre et al. (2002, p.
93) reported that birds that collided
with lights then fell to ground with fatal
injuries, were killed by predators, or
died of starvation, and that 94 percent
of these procellariids were juveniles.
Light-induced collisions and mortality
of storm-petrels at breeding locations
have been reported by researchers.
James-Veitch (1970, p. 40) reported that
ashy storm-petrels collided with a lamp
post on Southeast Farallon Island. Wolf
(2008, p. 8) reported personal
observations of storm-petrels flying
around the lighthouse light at West San
Benito Island, Mexico, a breeding
location for Leach’s and least stormpetrels. She also observed many
hundreds of dead storm-petrels that had
accumulated below the window that
enclosed the lighthouse light, after
attraction to the light and apparent
collision with the glass. The period over
which the storm-petrels collided with
and accumulated under the window is
unknown. Additionally, we are aware of
15 museum specimens of ashy stormpetrels that were collected at lighted
offshore energy platforms (n = 2) or
brightly lit coastal mainland locations (n
= 13) (Carter et al. 2000, p. 443;
Ornithological Information System
[ORNIS] 2008), and ashy storm-petrels
have been observed circling bright lights
at a coastal mainland sporting venue on
several occasions (Capitolo 2005, 2008;
LeValley 2008) (see following ‘‘At-sea
Artificial Light Pollution - Offshore
Energy Platforms’’ section). These
museum collections and direct
observations demonstrate that ashy
storm-petrels are attracted to light that
occurs far from ashy storm-petrel
breeding locations, where attendance by
storm-petrels is lower than at breeding
locations. Therefore, it is reasonable to
assume that near breeding locations
ashy storm-petrels are similarly
attracted to commercial fishery lights,
and that mortality of ashy storm-petrels
as a result of this attraction, although
not quantified, likely occurs.
Several researchers (Gross [1935, p.
387]; James-Veitch [1970, p. 65]; Ainley
[1995, p. 5]) have reported decreases in
the amount of aerial activities by stormpetrels at night at their nesting grounds
on bright, moonlit nights. Watanuki
(1986, pp. 14-22) showed that colony
activity levels of Leach’s storm-petrels
were inversely correlated with light
intensities and the corresponding risk of
predation by slaty-backed gulls (L.
schistisagus). Oro et al. (2005, p. 425)
reported that predation of European
storm-petrels (Hydrobates pelagicus) by
yellow-legged gulls (L. michahellis) was
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much higher at a cave that received
stronger illumination from the city of
Benidorm, Spain, located approximately
1.9 mi (3 km) from the storm-petrel
colony. Data in Keitt (2004, p. 176)
supported their hypothesis that a
function of nocturnal activity patterns
in the black-vented shearwater (Puffinus
opisthomelas) was reduction in the
likelihood of predation by western gulls.
Since procellariids have been shown to
use the cover of darkness as a defense
against predation at their nesting
colonies, it is paradoxical that
procellariids, including storm-petrels,
are also attracted to bright lights
(Montevecchi 2006, p. 94). Imber (1975,
p. 305) suggested that the attraction of
procellariids to bright lights is an
artifact of their visual cueing towards
bioluminescent prey.
Our review of the available
information revealed no direct
observations or evidence of mortality of
ashy storm-petrels through attraction to
squid fishery lights; however,
examining measures of reproductive
success provides indirect evidence of an
effect of squid fishery lights on ashy
storm-petrels at breeding locations.
From 1992 to 2000, Maxwell et al.
(2004, p. 665) documented intense
market squid harvesting near Santa
Rosa, Santa Cruz, Anacapa, and Santa
Catalina islands. During October 1995,
1996, and 1997, squid fishing activity
was relatively high along the north coast
of Santa Cruz Island from the west end
to Orizaba Rock (Maxwell et al. 2004, p.
668). At Orizaba Rock, the number of
active storm-petrel nest sites was 60
percent and 75 percent lower in 1997
than in 1995 and 1996, respectively
(McIver et al., in preparation), and the
numbers of active nests (counted during
mid-summer surveys) declined
significantly (10 percent per year) from
1996 through 2005 (Carter et al. 2007, p.
7). However, the number of ashy stormpetrel nests at Orizaba Rock increased in
2006 and 2007 (Carter et al. 2007, p. 7;
McIver et al. 2008, p. 6). Reasons for an
increase in numbers of active nests at
Orizaba Rock are not fully understood
and may reflect reduced use of bright
night lights, movements of some adult
storm-petrels from Bat Cave after skunk
predation in 2005, and other factors
(McIver et al. in preparation). Human
disturbance of nest sites on Orizaba
Rock has not been documented, so this
may not explain the reduction of nests
from 1996 to 2005. Based on our
conclusion that ashy storm-petrels are
less affected by such environmental
factors as reduced ocean productivity,
and the study by Adams and Takekawa
(2008, p. 14) that showed that ashy
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storm-petrels captured at three separate
breeding locations in southern
California forage in similar areas of
ocean, we believe it is unlikely that
oceanographic conditions explain the
reduced reproductive success and
numbers of nests of ashy storm-petrels
at Orizaba Rock. Our review of the
available information suggests that
bright lights used in the market squid
fishery at Orizaba Rock may have been
a factor in the observed decline in
numbers of active nests from 1996
through 2005, and low reproductive
success observed there in 1996 and
1997. However, our review of available
information did not reveal any data
regarding the reproductive success or
mortality rates of ashy storm-petrels at
other Southern California locations,
such as Santa Barbara Island and
adjacent Sutil Island, where larger
numbers of ashy storm-petrels nest than
at Oriziba Rock. The absence of any data
at these locations does not permit a
meaningful or reliable extrapolation of
trends regarding ashy storm-petrel
reproductive success and numbers of
active nests observed at Orizaba Rock,
including the possible effects of squid
fishery lights at that location, or to other
ashy storm-petrel nesting locations in
Southern California.
Acknowledging the potential for
impacts to breeding seabirds, the
MSFMP requires that squid fishery
boats in California limit wattage (per
boat) to 30,000 watts maximum and
maintain shields on lights that are
parallel to the deck of the vessel
(MSFMP 2005, Section 1-ii) in order to
reduce the potential for predation as a
result of illumination of seabird
breeding locations on islands adjacent
to fishing locations. However, ambient
and artificial light intensity at seabird
(including ashy storm-petrel) breeding
locations in California has not been
studied, and therefore the efficacy of the
MSFMP measures to reduce potential
predation associated with illumination
at islands is not known.
Measures to reduce the potential for
predation as a result of illumination of
seabird breeding locations, such as
reduced wattage of lights and reduced
upward radiation of light, are likely less
effective in reducing the potential for
attraction and collision of ashy stormpetrels that approach lighted fishing
boats. While foraging and while in
transit, ashy storm-petrels fly from a few
centimeters (inches) to a few meters
(yards) over the surface of the ocean,
and upon approaching lighted boats, are
exposed to the lights. Mortality to
breeding and non-breeding ashy stormpetrels could occur through direct
collision with lights, and ashy storm-
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petrels, exhausted after constant circling
of lights, could be susceptible to
predation by gulls, which are also
known to concentrate around lighted
squid fishery boats, presumably to feed
on squid (Shane 1995, p. 10; W. McIver,
personal observation). Two dead ashy
storm-petrels were collected from boats
at sea off the coast of southern
California, presumably due to attraction
to bright lights (ORNIS 2008).
Squid fishery activities also occur in
the southern part of Monterey Bay
between Point Pinos and Fort Ord
(Recksiek and Frey 1978, p. 9). Market
squid fishing in general coincides with
spawning events, and in central
California squid spawning occurs from
April to October (CDFG 2005, pp. 1-21).
During autumn months (generally
September and October), thousands of
ashy storm-petrels congregate in the bay
in deeper waters over the Monterey
Submarine Canyon (Roberson 1985, p.
43); depending on location, flocks
generally occur 3 to 25 mi (5 to 40 km)
away from squid fishing areas.
Shearwater Journeys, a bird-watching
concessionaire in Monterey, California,
observed large flocks (estimated 7,000 to
10,000 birds) of ashy storm-petrels in
September 2008 on Monterey Bay
(Shearwater Journeys 2008, https://
www.shearwaterjourneys.com/
index.shtml). Based on known attraction
of storm-petrels to boats and brightly lit
facilities on the mainland, there is the
potential for ashy storm-petrels in the
large flocks to be attracted to these lights
if boats are present at night in Monterey
Bay during autumn months. Assuming a
total population of 10,000 ashy stormpetrels, and autumn flock sizes of 4,000
to 7,000 ashy storm-petrels in Monterey
Bay, approximately 40 percent to 70
percent of the total population of ashy
storm-petrels theoretically could be
exposed to this potential threat. This
estimate includes ashy storm-petrels
that come from Southeast Farallon
Island only at this time of year for a
short time. However, market squid
fishing in Monterey Bay is largely
observed to occur during daylight hours
(CDFG 2008b, p. 20; Pacific Fishery
Management Council 2008, p. 44) rather
than at night, when ashy storm-petrels
exclusively feed. While attracting lights
may be used during daylight hours in
this fishery, because ashy storm-petrels
exclusively feed at night we do not
expect that ashy storm-petrels are
significantly affected by the market
squid fishery in Monterey Bay. As stated
above, we have no data indicating any
ashy storm-petrel mortality associated
with market squid fishing in Monterey
Bay and are aware of only two dead
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ashy storm-petrels collected from boats
at sea off of the Southern California
coast. Accordingly, based on our review
of the available information regarding
light pollution from market squid
fishery boats and tuna farms near ashy
storm-petrel breeding colonies, we
conclude that some low level of
mortality of ashy storm-petrels may be
occurring as a result of squid fishery
lighting, resulting in a temporaily
reduced number of birds within limited
geographic locations.
Approximately 26 percent to 34
percent of the total ashy storm-petrels at
breeding locations may be exposed to
lighting. This estimate does not include
ashy storm-petrels at Southeast Farallon
Island, where squid fishing is
prohibited. However, available data
does not indicate that the potential
threat from bright lights is causing
significant mortality to the overall
population of ashy storm-petrels.
Further, our review of the available
information does not suggest that the
threat of fishery-related lighting is
expected to increase to any large degree
in the foreseeable future due to
implementation of regulations limiting
wattage of lighting and location of
fishing activities. While not basing our
conclusion on this factor, we are aware
that the State of California has issued
regulations that limit the wattage of
lighting and location of fishing
activities. Therefore, we do not consider
artificial light pollution from the market
squid fishery or tuna aquaculture
operations to be a significant threat to
ashy storm-petrels at breeding colonies
anywhere within the species’ range at
this time.
At-sea Artificial Light Pollution Offshore Energy Platforms
The petitioner asserts that the ashy
storm-petrel’s marine environment is
being (and will be) modified and
degraded by artificial light pollution
from current (and future) offshore
energy platforms (oil production
platforms and liquefied natural gas
(LNG) terminals) and vessels (CBD 2007,
pp. 15-16). Specifically, the petitioner
claims that ashy storm-petrels are (or
would be) attracted to bright lights and
die from exhaustion after constant
circling of the lights, or die by direct
collision with the lights or platforms.
Offshore oil operations in California
are conducted from 23 platforms in
Federal waters (greater than 3 mi (4.8
km) from shore) and 10 platforms and
related facilities in State waters (less
than 3 mi (4.8 km)), distributed over an
area of about 7,700 square mi (20,000
square km) along the southern coast of
the State (McCrary et al. 2003, p. 43).
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All of the currently operational
platforms occur within the at-sea range
of foraging ashy storm-petrels (Briggs et
al. 1987; p. 23 Mason et al. 2007, pp. 5659; Adams and Takekawa 2008, pp. 1213). Offshore oil production platforms
in California are illuminated at night by
bright, incandescent lights that serve as
maritime navigational aids and
illuminate working platforms and
walkways.
Russell (2005, pp. 1-330) studied the
interactions between migrating birds
and offshore oil and gas platforms in the
northern Gulf of Mexico; however, our
review of the available information did
not reveal any surveys that have been
conducted to assess storm-petrel (or
other bird species) attraction to oil
production platforms off the coast of
California, or any direct observations of
ashy storm-petrels flying around the
lights of offshore oil production
platforms. However, Carter et al. (2000,
p. 443) reported two specimens of ashy
storm-petrels (archived at the Santa
Barbara Natural History Museum, Santa
Barbara, California (SBNHM)) that were
recovered dead on an offshore oil
platform (Platform Honda), located
approximately 5 mi (8 km) off the coast
of southern California. Ashy stormpetrels have also been collected dead
from mainland locations with bright
lights, indicating that the birds were
attracted to and died as result of
association with bright lights. Carter et
al. (2000, p. 443) reported six ashy
storm-petrel carcasses (also archived at
SBNHM) that were recovered from six
mainland locations (from Goleta to
Point Mugu) with bright lights in
southern California. The Service is
aware of at least seven additional
museum specimens of ashy stormpetrels that were collected at mainland
locations in California with bright
lights; all were collected during autumn
months (Ornithological Information
System [ORNIS] 2008). Ashy stormpetrels have also been observed flying at
night around bright lights at a stadium
adjacent to San Francisco Bay on several
occasions during autumn months over
the past several years (Capitolo 2005,
2008; LeValley 2008). LeValley (2005,
2008) described the storm-petrels as
juveniles, based upon plumage
characteristics, and observed on at least
two occasions that the storm-petrels
flew to and landed in the lights.
The museum specimens are evidence
that ashy storm-petrels are attracted to
bright lights, even those that occur in
metropolitan areas, far from their at-sea
foraging range. This indicates that bright
lights on oil production platforms that
occur within their marine range likely
attract more ashy storm-petrels than are
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indicated by random collection and
museum records. The direct
observations of ashy storm-petrels
around bright lights during autumn
months support an examination by
Imber (1975, p. 304), who states that
juvenile procellariids are likely attracted
to lights more often than adults.
Similarly, most of the museum
specimens from mainland locations and
the offshore platforms were collected in
the fall and may have been juvenile
birds. In a study of migratory passerine
birds in the Gulf of Mexico, Russell
(2005, p. 4) reported that offshore
platforms attract birds, induce nocturnal
circulations of platforms and result in
mortality of birds through collision.
This is commensurate with reported
observations of ashy storm-petrels flying
around and into bright lights at coastal
mainland sporting events. Field
demonstration tests on an offshore oil
platform in the North Sea, involving the
exchange of lighting with a greenish
light, and reductions in lighting, have
been shown to reduce passerine bird
occurrence at the platform by 50 to 90
percent (Marquenie and van de Laar
2004, p. 6; Marquenie et al. 2008, pp. 24). Our review of the available
information did not find any similar
demonstration on oil production
platforms in southern California.
Two LNG projects are proposed off
the coast of southern California
(California Energy Commission 2009).
The proposed Clearwater Port Project
(owned by Northern Star Natural Gas
Inc.) would be located approximately 13
mi (21 km) offshore of the City of
Oxnard, Ventura County, in the Santa
Barbara Channel. Clearwater Port would
reconfigure an existing offshore oil
production platform (Platform Grace).
Reconfiguration of the platform would
involve installing an LNG transfer
system, a cool down system, pumps,
and ambient air vaporizers, and
reinstalling and upgrading the
platform’s power-production capability.
The proposed Port Esperanza (owned by
Esperanza Energy, LLC, a subsidiary of
Tideland Oil & Gas Corporation) would
be located approximately 15 mi (24 km)
south of the port of Long Beach, and
would include two unmoored, selfpropelled, re-gasification units, each
connected to its own permanently
moored buoy. The application for a
third LNG project, the Oceanway LNG
Terminal Project, was withdrawn by
Woodside Petroleum Ltd., in January
2009 (Woodside Petroleum Ltd. 2009,
pp. 1-2). Our review of the available
information did not find specific plans
that describe the lighting configurations
of these proposed terminals, but
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assumes that lighting configurations and
intensities would be similar in nature to
current offshore oil platforms in
California.
As stated earlier, Le Corre et al. (2002,
p. 97) found that the geographic
distribution of the mortality to Barau’s
petrel (due to attraction to bright lights
at night) depended on location of urban
and industrial areas in relation to the
distribution of breeding colonies. At
´
Reunion Island, light sources were
urban, stationary, and functioned (at
night) continuously (Le Corre et al.
2002, p. 96). In southern California,
continuously functioning sources of
light include extensive mainland
metropolitan areas, and 33 offshore oil
production platforms (McCrary et al.
2003, p. 43). The oil production
platforms are located within 150 mi
(240 km) of all southern California ashy
storm-petrel breeding locations, well
within the distance from breeding
colonies that the species has been
observed to forage (220 mi [360 km])
(Adams and Takekawa 2008, p. 13).
Accordingly, we conclude that about 50
percent of the total population of ashy
storm-petrels (approximately 100
percent of the ashy storm-petrels that
breed in the California Channel Islands)
may be exposed to this potential threat.
In summary, based on observations of
ashy storm-petrels collected dead from
an offshore oil platform and from
brightly lit mainland locations, and
recent observations of ashy stormpetrels observed in association with
bright lights at a sporting facility, we
have information that ashy storm-petrels
are susceptible to bright lights on
current structures that occur in their
oceanic environment. This threat likely
results in some (but unknown) level of
mortality. At this time, the existing
population information does not
indicate that mortality associated with
offshore energy platforms is a significant
threat to the species at Southeast
Farallon Island, at the Channel Islands,
or rangewide. However, should offshore
energy development increase
significantly in the future, it would
likely be appropriate to monitor and
provide conservation measures that
would eliminate or minimize the
potential for mortality.
Oil Pollution – Offshore Energy
Production Platforms
The largest oil spill from offshore oil
operations in California was the 80,000barrel (3,360,000-U.S. gallon) Santa
Barbara spill from Platform A in 1969,
which resulted in the death of
thousands of birds (McCrary et al. 2003,
p. 46). Since 1969, only one spill from
oil and gas operations offshore of
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California has resulted in documented
seabird mortality (more than 700 birds),
the 163-barrel (7,000-gallon) Platform
Irene pipeline spill, off Point Arguello
in 1997 (Torch/Platform Irene Trustee
Council 2007, p. 3; McCrary et al. 2003,
p. 46). Oiled ashy storm-petrels were
not documented during either of these
spills. Applying information on
estimated spill size and spill probability
to potential impacts on seabirds is
difficult because of many factors,
including the type, rate, location, and
volume of oil spilled, weather and
oceanographic conditions, timing
within year of the spill, distribution of
seabird species near a spill, and
behavior of seabirds in reaction to oil
slicks (Ford et al. 1987, p. 549; McCrary
et al. 2003, p. 46). Minerals
Management Service (2001, p. xix)
reported that without the development
of 36 currently undeveloped leases, the
probabilities that one or more oil spills
will occur from existing Outer
Continental Shelf oil and gas activities
(during years 2002 to 2030) are 73.9
percent for a spill of 200 barrels (8,600
U.S. gallons) or less, and 59.1 percent
for a spill of 2,000 barrels (86,000 U.S.
gallons).
A Federal moratorium on offshore
drilling and platform development off
the coast of California was initiated by
the U.S. Congress in 1982 (U.S.
Department of Energy 2005). On October
1, 2008, the 1982 offshore drilling
moratorium expired and was not
renewed by the U.S. Congress. On
September 16, 2008, the U.S. House of
Representatives passed bill H.R. 6899,
the Comprehensive American Energy
Security and Consumer Protection Act,
which would allow oil and natural gas
exploration and production between 50
and 100 mi (80 and 161 km) off the U.S.
coasts. The U.S. Senate has received but
not yet voted on H.R. 6899. Fossil fuel
(such as petroleum and natural gas)
energy use and production is and will
likely continue to be a significant
societal issue for the United States in
the foreseeable future. Consequently, it
is foreseeable that within the next 15
years, additional offshore oil and gas
platform development will occur off the
California coast, within the marine
range of ashy storm-petrels.
Based on information available to the
Service regarding offshore oil
production, we conclude that about 50
percent of the total population of ashy
storm-petrels could potentially be
exposed to oil spills. However,
predicting the possible effects of an oil
spill from an offshore energy production
platform is difficult and would depend
on the timing and amount of a spill,
prevailing ocean currents and
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the S.S. Luckenbach occurred every few
years from 1973 through 2002
(Luckenbach Trustee Council 2006, pp.
i, 65). Small seabirds (including ashy
storm-petrels) may be more susceptible
to mortality due to predation after
oiling, and the degree of at-sea loss is
likely higher with offshore species (Ford
et al. 1987, pp. 549-550). Although
specific mortality for ashy storm-petrels
Oil Pollution - Vessels
was not estimated during the S.S.
Hampton et al. (2003, p. 29)
Luckenbach spill event, it was
summarized previous reports and
presumed that the ratio of actual dead
showed that, during the 20th century,
to recovered dead was similar to that of
hundreds of thousands to millions of
ancient murrelets (Synthliboramphus
seabirds, especially common murres
antiquus) and Cassin’s auklets, and that
(Uria aalge), were killed by oil pollution total mortality for ashy storm-petrels
from oil tankers and other marine
was approximately 21 individuals
vessels in central California. Hampton et (Luckenbach Trustee Council 2006, p.
al. (2003, p. 30) estimate that
65).
approximately 20 tankers per week
Based on information available to the
arrive at and depart ports in California.
Service regarding oil tanker traffic off
In California, large oil transfer facilities
the coast of California, ashy stormoccur in San Francisco Bay and Long
petrels are exposed to the threat of oil
Beach Harbor (Los Angeles) (California
spills. In addition, because oiled ashy
Resources Agency 2008, p. 5F-6). Ports
storm-petrels have been recovered from
for non-tanker marine vessels (e.g.,
vessel-related spills (the S.S
dredges, cargo vessels) occur at
Luckenbach), we know that the species
numerous locations along the California is susceptible to oiling. Predicting the
and northwestern Baja California coasts. possible effects of an oil spill from
Tankers traveling along the coast, in
tankers is difficult and would depend
accordance with a voluntary agreement
on the timing and amount of a spill,
with California State and U.S. Federal
prevailing ocean currents and
agencies, stay about 50 mi (80 km)
conditions, and locations of ashy stormoffshore (Hampton et al. 2003, p. 31).
petrels at the time of a spill. Since
Hampton et al. (2003, p. 30) showed that thousands of ashy storm-petrels
oil spill accidents regarding non-tanker
congregate in Monterey Bay every fall,
vessels are the most common in
the species could be vulnerable to a
California, and that small volumes of oil tanker spill near Monterey Bay at that
may kill large numbers of birds. In an
time of year. However, the Service has
examination of shipping practices,
no information indicating that tanker
Hampton et al. (2003, pp. 30-32)
spills in the Monterey Bay are
suggested that the dumping of tanker
predictable or even likely. Therefore, we
washings could occur several times per
consider oiling from tanker spills to be
week off the California coast, regular
insignificant to ashy storm-petrels
tank washings could produce the
anywhere within the species’ range.
equivalent of a small (~10,000-U.S.
Organochlorine Contaminants
gallon) oil spill, and that dumping of
The petitioner asserts that the ashy
tanker washings could pose a greater
storm-petrel is threatened or endangered
threat to offshore (e.g., greater than 50
by the presence, in the marine
mi (80 km) out) seabird species,
environment, of organochlorine
including ashy storm-petrels, than to
pollutants—specifically,
species occurring closer inshore.
dichlorodiphenyltrichloroethane (DDT),
Minerals Management Service (2001, p.
polychlorinated biphenyls (PCBs), and
xix) reported a 90.5 percent probability
of a 22,800-barrel (957,600 U.S. gallons) their breakdown products (CBD 2007, p.
18). The petitioner asserts that, as a
tanker spill occurring in waters of the
result of the presence of these pollutants
Outer Continental Shelf during 2002 to
in the waters off California, eggshell
2030.
Oiled ashy storm-petrels have been
thinning occurred in collected eggs of
collected in California. Two ashy storm- the ashy storm-petrel, and reproductive
petrels were collected between 1997 and success of the species has been reduced
2003, in association with ‘‘mystery
(CBD 2007, p. 19).
During the period from the late 1940s
spills’’ attributed to the S.S. Jacob
to the early 1970s, Los Angeles area
Luckenbach, which sank in the Gulf of
the Farallones in 1953 and leaked oil as industries discharged and dumped
thousands of tons of DDT and PCBs into
it decayed on the ocean floor
ocean waters off the Southern California
(Luckenbach Trustee Council 2006, pp.
coast (Department of Commerce 2001, p.
i, 65). Major oiling events attributed to
conditions, and locations of ashy stormpetrels at the time of a spill. We
conclude that a relatively small
proportion of the population would
likely be exposed to any single oil spill,
and consequently oil spills are not
considered to be a significant threat to
ashy storm-petrels anywhere within the
species’ range.
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51391). Almost all of the DDT originated
from the Montrose Chemical
Corporation’s manufacturing plant in
Torrance, California, and was
discharged into Los Angeles County
sewers that empty into the Pacific
Ocean at White Point, on the Palos
Verdes shelf (Department of Commerce
2001, p. 51391). In addition, large
quantities of PCBs from numerous
sources throughout the Los Angeles
basin were released into ocean waters
through the Los Angeles County sewer
system (Department of Commerce 2001,
p. 51391).
Most organochlorine pesticides are
hydrophobic (meaning that they tend
not to combine with, or are incapable of
dissolving in water) and show a high
affinity for lipids (Portman and Bourne
1975, p. 294). Bioaccumulation is
defined as an increase in the amount of
a substance in an organism or part of an
organism that occurs because the rate of
intake exceeds the organism’s ability to
remove the pesticide from the body
(Holland 1996, p. 1170).
Biomagnification is defined as the
bioaccumulation of a pesticide through
an ecological food chain by transfer of
residues from the diet into body tissues,
in which the tissue concentration
increases at each trophic level in the
food web (Holland 1996, p. 1171).
Storm-petrels feed on prey that occur at
the ocean’s surface and that contain
high concentrations of lipids, such as
euphausiids, larval fish, fish eggs, and
squid (Watanuki 1985, p. 885; Warham
1990, p. 186). As mentioned in the
Species Description section above, the
diet of ashy storm-petrels has not been
well-studied, but likely includes
euphausiids, larval fish, and fish eggs,
which would make ashy storm-petrels
susceptible to bioaccumulation and
biomagnification.
Eggshell thinning caused by DDE
(dichlorodiphenyldichloroethylene, a
metabolite of DDT), which results in
eggs getting crushed during incubation
and thus breeding failure of many fisheating birds, is probably the best
documented effect of environmental
pollutants on birds (Fry 1995, p. 168).
DDT-induced eggshell thinning caused
reproductive failures of brown pelicans,
bald eagles, and peregrine falcons in the
California Channel Islands (Hickey and
Anderson 1968, pp. 271-273;
Risebrough et al. 1971, pp. 8-9; Gress et
al. 1973, pp. 197-208).
Coulter and Risebrough (1973, pp.
254-255) first reported eggshell thinning
in the ashy storm-petrel in the early
1970s. Ashy storm-petrel eggs were also
collected for contaminant analyses and
measurements of eggshell thinning in
1992 (Fry 1994; Kiff 1994), 1995-97 (D.
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Welsh, unpublished data), and 2008
(Cater et al. 2008). For eggs collected in
1992, the highest levels of total DDT and
PCBs, relative to other seabird species,
were contained in ashy storm-petrel
eggs, and the averages for total DDT and
PCBs in ashy storm-petrel eggs were the
highest measured for any of the 13
species that were examined, and
measured almost twice the levels
observed in the second-most
contaminated eggs (Fry 1994, p. 30). Kiff
(1994, pp. 1-29) compared eggshell
thicknesses of ashy storm-petrel eggs
that were collected before 1947 (precontamination reference material) to
eggshell thicknesses of eggs collected in
1992 and reported that 27.8 percent of
the ashy storm-petrel eggs collected
from Santa Cruz Island (n = 18) were 15
percent thinner than the pre-1947
average. Concentrations of DDE in ashy
storm-petrel eggs have been linked with
eggshell thinning and lower hatching
success (Carter et al. 2008c, p. 4). Based
on findings from 12 ashy storm-petrel
eggs collected in 2008, Carter et al.
(2008, p. 4) reported statistically
significant declines (p<0.0001) in levels
of DDE and PCBs in ashy storm-petrel
eggs collected in 2008, compared to eggs
collected in the 1990s. Data are
currently not available on eggshell
thicknesses of ashy storm-petrel eggs
collected in 2008, but the Service
anticipates that additional work will be
funded in 2009 to further analyze
organochlorine contaminant data and
examine changes in eggshell thinning in
randomly collected and salvaged eggs.
Carter et al. (2008, p. 5) speculated
organochlorine contaminant
concentrations from the 1960s to the
1980s were greater in ashy stormpetrels, as compared to other breeding
seabirds in southern California, such as
brown pelicans (Pelecanus occidentalis)
and double-crested cormorants
(Phalacrocorax auritus). Organochlorine
contaminant levels and reproductive
success of ashy storm-petrels in
southern California were not measured
or monitored prior to the 1990s;
however, Carter et al. (2008, p. 5)
suggest that higher organochlorine
concentrations may have contributed to
lower hatching success and lower
population size of ashy storm-petrels in
southern California during the 1960s to
1980s than observed in the 1990s.
During 1995 to 1997, a higher
proportion of broken eggs were found
than in 2005 to 2007 (McIver et al. in
preparation). McIver et al. (in
preparation) reported that hatching
success at Santa Cruz Island differed
significantly among years, with lowest
success in 1996 (53.5 percent, n = 187)
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and highest success in 2006 (82.0
percent, n = 61). McIver et al. (in
preparation) speculated that DDEinduced eggshell thinning likely
contributed to lower hatching success at
Santa Cruz Island from 1995 to 1997
and likely explained (in part) the
relatively high proportion of broken
eggs found at all Santa Cruz Island
locations monitored. Carter et al. (2008,
p. 5) concluded that DDE and total PCBs
decreased to much lower levels between
1992 and 2008, and that, from 1992 to
1997, relatively high contaminant levels
and associated eggshell thinning and
premature embryo deaths likely were
significant contributing factors to
relatively low hatching success
observed during this period.
Based on information available to the
Service regarding organochlorine
contamination of ashy storm-petrels,
ashy storm-petrels have been exposed
(likely, through their food resources) to
organochlorine contaminants
throughout their foraging range, but this
exposure has likely been greater for ashy
storm-petrels breeding in southern
California and foraging in nearby
waters. We conclude that
organochlorine contaminants are still
present in ashy storm-petrels, but
preliminary results indicate that current
levels of contaminants are much
reduced compared to levels observed in
the 1990s. In addition, fewer numbers of
broken eggs and higher hatching success
of ashy storm-petrels at Santa Cruz
Island may be explained, in part, by
reduced organochlorine contamination.
Therefore we consider this threat to be
insignificant to ashy storm-petrels at
Southeast Farallon Island, at the
Channel Islands, or rangewide.
Ingestion of Plastics
The petitioner asserts that the ashy
storm-petrel is threatened by the
ingestion of plastic particles floating at
the ocean’s surface (CBD 2007, pp. 2021). Ingestion of plastics by seabirds is
well-documented, and plankton-feeding
seabirds, such as ashy storm-petrels, are
more likely to confuse plastic pellets for
their prey than are fish-eating seabirds;
therefore, the plankton-feeding seabirds
show a higher incidence of ingested
plastics (Azzarello and Van Vleet 1987,
p. 295). Two studies have documented
the presence of plastic particles in
storm-petrel species that foraged in
waters of the California Current. Blight
and Burger (1997, p. 323-324) dissected
seabirds caught as bycatch in the eastern
North Pacific; they found plastic in all
eight storm-petrel (Leach’s and forktailed) carcasses they collected, and the
number of pieces of plastic in each bird
was highest for the two species of storm-
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petrels and in a Stejneger’s petrel
(Pterodroma longirostris). Shuiteman
(2006, p. 23) found plastic particles in
regurgitation samples of Leach’s stormpetrels caught in mist nets on Saddle
Rock, Oregon.
At-sea surveys for plastic particles off
the coast of southern California (Moore
et al. 2004, pp.1-6) in 2000 and 2001 are
the only research that the Service is
aware of that has attempted to quantify
the amount of plastics observed in
waters within or near the foraging range
of ashy storm-petrels. Moore et al.
(2004, pp. 2-3) reported densities of up
to 7.25 pieces per cubic meter of water
sampled for plastic pieces that were less
than about 0.2 inches (5 millimeters) in
diameter. As stated in the Species
Description section above, like other
storm-petrel species, ashy storm-petrels
feed by picking prey from the surface of
the ocean. Because plastic ingestion by
storm-petrels has been welldocumented, we assume that ashy
storm-petrels also ingest plastic.
However, the incidence of plastic
ingestion by ashy storm-petrels has not
been specifically evaluated (such as by
necropsy or analysis of regurgitations).
In addition, plastic ingestion has not
been reported as a cause of death of
ashy storm-petrel chicks or adults
(Ainley et al. 1990, pp. 128-162; McIver
2002, pp. 17-49), and the degree to
which the ingestion of plastic may affect
ashy storm-petrels is not known (Ainley
1995, p. 9).
Based on information available to the
Service regarding the presence and
availability of plastic particles in the
marine environment used by ashy
storm-petrels, and the propensity for
storm-petrels to ingest plastic, we
recognize that nearly all ashy stormpetrels have the opportunity to ingest
plastic, but we have no information on
the rate of ingestion. We also recognize
plastic particles will continue to be
ubiquitous in the future in the waters of
the California Current, where ashy
storm-petrels feed. Although plastic
ingestion has been observed in other
species of storm-petrels and likely
occurs with ashy storm-petrels, our
review of the available information
revealed no direct evidence that
suggests ashy storm-petrels are currently
being negatively affected by this
potential threat. Therefore, we consider
this threat to be insignificant to ashy
storm-petrels at Southeast Farallon
Island, at the Channel Islands, or
rangewide.
Summary of Factor E
Regarding other natural or manmade
factors affecting the continued existence
of the species, the Service concludes
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that the presence of bright lights
associated with commercial fishing
operations (for example, market squid
fishery and tuna aquaculture) at ashy
storm-petrel breeding locations and (to
a lesser extent) near large at-sea
congregations of ashy storm-petrels,
causes mortality in adult and fledgling
ashy storm-petrels through direct
collision with lights and predation, but
is unlikely to affect the species at a
population level.
The Service concludes that the
presence of constantly shining lights (at
night) on oil and gas production
platforms (current and future) off the
California coast, causes mortality in
foraging ashy storm-petrels, which may
collide with lights or become exhausted
after constant association with the
lights. However, there is no information
suggesting that populations are
currently unstable or decreasing as a
result of these mortality sources.
The Service concludes that potential
oil spills from existing or proposed
platforms pose a threat to small
numbers of ashy storm-petrels off
southern California, and that spills from
oil tankers moving off the coast of
California may pose a threat to foraging
and flocking ashy storm-petrels. The
scale of threat would depend on the
size, location, and timing within year of
the spill. The Service concludes that it
is unlikely that such oil spills will be of
a size that would pose a significant
threat to ashy storm-petrels.
The Service concludes that
organochlorines still contaminate eggs
of ashy storm-petrels but that current
observed levels of contaminants are
reduced, compared to levels observed in
eggs collected during the 1990s, and
that organochlorine contamination does
not appear to be reducing hatching
success of ashy storm-petrels. The
Service concludes that, like other stormpetrels, ashy storm-petrels likely ingest
plastic while foraging, but the degree to
which plastic ingestion threatens ashy
storm-petrels is not known and is not
considered to be a threat. Finally, we
have no reason to believe that any of
these threats are likely to increase in the
foreseeable future. Therefore, we
consider these threats to be insignificant
to ashy storm-petrels at Southeast
Farallon Island, at the Channel Islands,
or rangewide.
Foreseeable Future
In considering the foreseeable future
as it relates to the status of the ashy
storm-petrel, we take into consideration
our analysis of the potential threats to
the species as described above. No data
are currently available regarding adult
life span of the species; however, ashy
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storm-petrels are thought to live on the
order of 20 to 25 years (Sydeman et al.
1998b, p.7). Oceanographic and climatic
processes potentially affecting ashy
storm-petrels operate on the order of
single year to multi-decadal scales. For
example, the marine environment off
the west coast of North America is
affected by oceanographic processes,
˜
˜
such as El Nino and La Nina, which
occur on annual scales, and the Pacific
Decadal Oscillation, which occurs on
decadal scales. Based on historical and
recent trends of oceanographic
˜
phenomena, such as El Nino events, and
our above analysis of how ashy storm˜
petrels are affected by El Nino events,
we conclude the potential threat from
changes in the ocean environment over
the timescales at which they currently
operate are not significant to the ashy
storm-petrel.
Principle among the potential threats
to the ashy storm-petrel is mortality
from avian predators. There was likely
a decline in the population of ashy
storm-petrels at Southeast Farallon
Island in the mid-1970s to the early
1990s (Sydeman et al. 1998a, p. 443).
However, more recent data (Warzybok
and Bradley 2007, p. 17) suggest an
increasing population of ashy stormpetrels at Southeast Farallon Island.
Additionally, mortality due to predation
from owls seems to show a decreasing
trend over recent years, and mortality
due to predation from skunks is likely
a sporadic event without a specific
identifiable time element. Given these
recent trends, we do not expect an
increase in mortality of ashy stormpetrels in any one location or across
their range.
Ashy storm-petrel breeding locations
occur primarily on federally owned and
managed lands in the United States and
Mexico. A broad network of Federal,
State, and International protections have
been and are currently in place that
protect the ashy storm-petrel. Based on
historical and recent trends of land
management policies on federally
owned lands in the United States, we
find it unlikely that substantial changes
to current land management practices or
regulations that would negatively affect
ashy storm-petrels are likely to occur in
the near term, and any changes are most
likely on the order of decades in the
future.
Based on the trend to restrict use of
attracting lights used in the market
squid fishery, we conclude this
potential threat is not likely to increase
over time. The threat of eggshell
thinning from organochlorine exposure
has steadily decreased over time and is
not likely to increase in the future
because their use is banned. The
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incidence of oil spills of sufficient size
to significantly affect ashy storm-petrels
is largely stochastic. There is no
evidence of an increasing trend in the
incidence of spills, and based on
increased measures to ensure the safety
of oil and gas transportation, we do not
consider this potential threat to increase
in the future. Plastics ingestion is
currently not a significant threat to the
ashy storm-petrel and, based on historic
information, we do not believe this
threat would increase in the future.
Therefore, we consider the foreseeable
future to encompass the timeframe over
which the effects of potential threats as
described above can be reasonably
anticipated.
Finding
We assessed the best available
scientific and commercial information
regarding threats faced by the ashy
storm-petrel. We reviewed numerous
information sources including literature
cited in the petition, information in our
files, and information submitted to us
following our 90–day petition finding
(73 FR 28080; May 15, 2008) related to
potential threats to the ashy storm-petrel
(climate change, ocean acidification, sea
level rise, predation, light attraction,
contamination by chlorinated
hydrocarbons, and plastic pollution) on
ashy storm-petrels and the California
Current marine environment.
We found evidence that the ashy
˜
storm-petrel is less affected by El Nino
events than most seabirds in the
California Current System. This is not to
imply that ashy storm-petrels are not
˜
affected by El Nino events; fewer
numbers of ashy storm-petrels may
˜
attempt to breed during El Nino events,
and timing of breeding within year may
be slightly delayed. However, ashy
storm-petrels show low between-year
variability in fledgling production, and
unlike other seabirds, have bred in
every year for which there are
observations of nesting activities.
Because ashy storm-petrels forage over a
wide geographic area and have an
extended egg-laying and chick-rearing
period, they are likely more able to
exploit prey resources that may be more
scarce and patchily distributed. Ocean
acidification is occurring, but current
research does not demonstrate a link
between ocean acidification and
reduced abundance and survival of prey
items on which ashy storm-petrels
depend, nor does our analysis or current
research indicate that reproductive
success of ashy storm-petrels is affected
by ocean acidification. Based on current
projections of sea level rise that predict
a 3-ft (0.9-m) rise by 2100, we found that
the majority of nesting habitat is at least
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4.9 ft (1.5 m) above current sea level.
The exception is some nesting habitat in
the Channel Islands at Cavern Point
Cove Caves that may become
submerged. However, this location
represents a small percentage of the
rangewide nesting population, and we
do not consider this to be a significant
threat. Introduced grasses are present on
Southeast Farallon Island; however, we
do not have specific information that
quantifies the amount of suitable
nesting habitat at Southeast Farallon
Island, or other breeding locations, that
may be unavailable to ashy stormpetrels because of introduced grasses. In
addition, the petitioner claims that
introduced grasses are widespread at all
breeding locations. For example, grasses
do not occur in sea caves or on most
offshore rocks where ashy storm-petrels
nest.
Therefore, we find that the ashy
storm-petrel is not threatened by the
present or threatened destruction,
modification, or curtailment of the
species’ habitat or range, now or in the
foreseeable future.
While collection of ashy storm-petrel
adults and eggs has occurred throughout
its breeding range over the past 124
years, the rate of specimen collection
has been low and sporadic and not
concentrated in any one location. The
number of specimens collected to date
is very small compared to the current
estimated total population size.
Consequently, we find that the ashy
storm-petrel is not threatened by
overutilization of the species for
commercial, recreational, scientific, or
educational purposes now or in the
foreseeable future.
Predation by western gulls and owls
at Southeast Farallon Island does not
pose a significant threat to the ashy
storm-petrel. Although populations of
ashy storm-petrels at Southeast Farallon
Island may have decreased from 1979 to
1992 as a result of predation, we find
that the best available scientific
information indicates that populations
are increasing in recent years. While
predation of ashy storm-petrels is likely
to continue within the foreseeable
future, we find that predation at
Southeast Farallon Island is not a
significant threat to the species.
Mortality due to predation by island
spotted skunks at Santa Cruz Island is
not a significant threat to the ashy
storm-petrel. Although sporadic island
spotted skunk predation events will
likely continue over time, there is no
information suggesting that spotted
skunk predation is a significant threat to
the species. We found evidence that
deer mice and house mice are likely
predators or scavengers of small
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numbers of ashy storm-petrel eggs and
small chicks, but this likely does not
substantially affect the productivity of
the species. Consequently, we find that
the ashy storm-petrel is not threatened
by disease or predation now or in the
foreseeable future.
Based on our review of the best
available information, we find there is a
network of existing regulatory
mechanisms that serve to protect the
species. As much as 75 percent of ashy
storm-petrel breeding locations are
included in marine reserves designed to
limit the use of bright lights associated
with squid fishery activities, and the
implementation of the Market Squid
Fishery Management Plan should be
effective in offering protection for ashy
storm-petrels. We found no support for
the petitioner’s claim that a lack of
regulatory mechanisms regarding the
MBTA poses a threat to the ashy stormpetrel. While compliance with MBTA is
not universally applied, this law
provides protections from killing,
taking, and possessing the ashy stormpetrel. We find that a lack of regulatory
mechanisms to control GHG does not
threaten the ashy storm-petrel, because
we determined that processes associated
with climate change, such as ocean
acidification, sea level rise, and possible
increases in sea surface temperatures
(see Factor A) have not been shown to
directly impact the ashy storm-petrel.
Therefore, we find the ashy storm-petrel
is not threatened by the inadequacy of
existing regulatory mechanisms.
Ashy storm-petrels are attracted to
bright lights. Bright lights associated
with the market squid fishery may result
in the reduced number of birds within
specific geographic areas; however, our
review of the available information does
not indicate that the threat from market
squid fishery lighting is contributing to
mortality that results in large-scale
population declines. Ashy storm-petrels
that congregate in Monterey Bay in the
fall months do not appear to be at
particular risk from squid fishing
activities because the available
information indicates much of the
fishing occurs during the day, whereas
ashy storm-petrels feed exclusively at
night. Bright lights on offshore energy
platforms may contribute to small levels
of ashy storm-petrel mortality; however,
we found no indication that this is a
significant threat to the species.
Furthermore, our review of the available
information does not suggest that the
threat of lighting from the market squid
fishery or other sources is expected to
increase to any large degree in the
foreseeable future. Therefore, we do not
consider bright lights associated with
market squid fishing or offshore energy
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platforms to be a significant threat to the
ashy storm-petrel.
We find oil pollution does not pose a
significant threat to the ashy stormpetrel. Although there is a high
probability of spills from oil production
platforms or tankers within the range of
foraging ashy storm-petrels, this source
of mortality is not expected to result in
severe impacts to major portions of the
population. We conclude that a
relatively small proportion of the
population would likely be exposed to
any single oil spill, and, consequently,
oil spills are not considered to be a
significant threat to ashy storm-petrels.
We find organochlorine contamination
does not pose a significant threat to ashy
storm-petrel, because this threat likely
occurred in the past, is currently much
reduced, and that contamination of ashy
storm-petrels by organochlorines
currently does not significantly reduce
hatching success. Ingestion of plastic by
ashy storm-petrels does not pose a
significant threat to the species. We
found evidence that small plastic
particles occur at the ocean’s surface
within the feeding range of ashy stormpetrels, and we found that many species
of procellariids, including storm-petrels,
ingest plastics. It is likely that ashy
storm-petrels ingest plastic while
foraging; however, we found no direct
evidence, such as dead chicks or adults,
underweight chicks or adults, or
observation of plastics in regurgitations
that indicates that plastic ingestion is a
threat to ashy storm-petrels. Therefore,
we find the ashy storm-petrel is not
threatened by other natural or manmade
factors now or in the foreseeable future.
On the basis of our status review, we
conclude the listing of the ashy stormpetrel rangewide is not warranted.
Significant Portion of the Range (SPR)
Analysis
The Act defines an endangered
species as one ‘‘in danger of extinction
throughout all or a significant portion of
its range,’’ and a threatened species as
one ‘‘likely to become an endangered
species within the foreseeable future
throughout all or a significant portion of
its range.’’ Having determined that the
ashy storm-petrel does not meet the
definition of a threatened or endangered
species, we must now consider whether
there are any significant portions of the
range where the species is in danger of
extinction or likely to become so in the
foreseeable future.
On March 16, 2007, a formal opinion
was issued by the Solicitor of the
Department of the Interior, ‘‘The
Meaning of ‘In Danger of Extinction
Throughout All or a Significant Portion
of Its Range’ ‘‘ (DOI 2007). We have
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summarized our interpretation of that
opinion and the underlying statutory
language below. A portion of a species’
range is significant if it is part of the
current range of the species and is
important to the conservation of the
species because it contributes
meaningfully to the representation,
resiliency, or redundancy of the species.
The contribution must be at a level such
that its loss would result in a decrease
in the ability of the species to persist.
The first step in determining whether
a species is endangered in an SPR is to
identify any portions of the range of the
species that warrant further
consideration. The range of a species
can theoretically be divided into
portions in an infinite number of ways.
However, there is no purpose in
analyzing portions of the range that are
not reasonably likely to be significant
and threatened or endangered. To
identify those portions that warrant
further consideration, we determine
whether there is substantial information
indicating that (i) the portions may be
significant and (ii) the species may be in
danger of extinction there. In practice, a
key part of this analysis is whether the
threats are geographically concentrated
in some way. If the threats to the species
are essentially uniform throughout its
range, no portion is likely to warrant
further consideration. Moreover, if any
concentration of threats applies only to
portions of the range that are
unimportant to the conservation of the
species, such portions will not warrant
further consideration.
We acknowledge that the Ninth
Circuit Court of Appeals decision in
Defenders of Wildlife v. Norton, 258
F.3d 1136 (2001) can be interpreted to
require that in determining whether a
species is threatened or endangered
throughout a significant portion of its
range, the Service should consider
whether lost historical range (as
opposed to current range) constitutes a
significant portion of the range of the
species at issue. While this is not our
interpretation of the case or the statute,
we conclude that there are no such areas
for the ashy storm-petrel. We have no
evidence to suggest that the occupied
range of the ashy storm-petrel is
different from its historical range, and
there is no evidence to suggest a range
contraction for the species. Therefore,
we will not further consider lost
historical range as a significant portion
of the species range.
The ashy storm-petrel breeds in two
main geographic areas: in the northern
portion of the species range on
Southeast Farallon Island, where
approximately 36 to 53 percent of the
entire population occurs, and in the
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Fmt 4702
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41859
southern portion of the species range on
the California Channel Islands, where
approximately 44 to 60 percent of the
breeding population occurs. About 1.5
to 2 percent nests in Mexico. The two
California areas are geographically
separated by approximately 250 miles
(402 km); however, there is no
indication that the populations are
genetically different, which is logical,
since the ashy storm-petrel ranges
widely in foraging activities. Southeast
Farallon Island is located in the
California Current, a cold water current;
in contrast, the California Channel
Islands are more affected by the
Davidson Current, which is a
comparatively warm water current. No
other areas within the species’ range
contain a significant number of breeding
locations. Ashy storm-petrels occur at
their breeding colonies nearly yearround and occur in greater numbers
from February through October (Ainley
1995, p. 5). For this reason, we consider
breeding locations to be most significant
to the species. The loss of all breeding
ashy storm-petrels at either Southeast
Farallon Island or in the Channel
Islands would reduce the rangewide
population of the species by
approximately 50 percent, which could
result in a decrease in the ability of the
species to persist.
To determine whether Southeast
Farallon Island or the Channel Islands
may warrant further consideration as a
significant portion of the range, we
evaluated these two areas of the range
of the ashy storm-petrel. Under our fivefactor analysis for the ashy storm-petrel
rangewide, we did not find any threats
that were significant to the species
rangewide or that were concentrated in
any one particular area. The potential
threat of ocean acidification, and
reduced ocean primary productivity, is
a rangewide threat that we concluded
was not significant. This is due to the
ability of the ashy storm-petrel to forage
more widely than other species and
because the ashy storm-petrel has not
demonstrated population breeding
failures as seen in other seabird species.
The threat of human degradation of
nesting habitats may be more evident in
the Channel Islands as compared to
Southeast Farallon Island, but we did
not find it to be a significant threat in
either area. We did find potential threats
were different in the northern portion of
the range compared to the southern
portion of the range. Our rangewide
analysis was conducted at a steppeddown geographic scale due to the
natural concentration of breeding birds
at Southeast Farallon Island and in the
Channel Islands. On Southeast Farallon
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Island, we identified a potential threat
of mortality due to predation by western
gulls and burrowing owls. Populations
of ashy storm-petrels at Southeast
Farallon Island may have decreased
from 1979 to 1992 as a result of
predation (Sydeman et al. 1998a, p.
443); however, more recent information
suggests that populations are increasing
in recent years (Warzybok and Bradley
2007, p. 17). Predation of ashy stormpetrels is likely to continue within the
foreseeable future; however, as
described above in our five-factor
analysis of the rangewide population,
we find that predation at Southeast
Farallon Island is not a significant threat
to the species. This particular predation
threat from western gulls is not found in
the Channel Islands; however, although
predation from skunks was identified as
a potential threat, we found it not to be
a significant threat. Rising sea levels due
to climate change may affect a small
portion of the breeding population in
the Channel Islands, but the large
majority of nesting sites are above
projected sea level rise into 2100. The
use of bright, attracting lights in the
market squid fishery was identified as a
potential threat to breeding birds in the
Channel Islands, but not to breeding
birds on Southeast Farallon Island due
to regulatory restrictions around the
island. Our analysis of the potential
threat of squid boat lights to ashy storm-
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petrels in the Channel Islands
concluded that some low level of
mortality may occur, but our review of
the available information did not
indicate that any such mortality would
lead to a large-scale population decline
and we found that adequate regulatory
protections are in place. The threat of an
oil spill is greater in the Channel Islands
due to a greater concentration of oil
producing facilities; however,
predicting the possible effects of an oil
spill from an offshore energy production
platform is difficult and would depend
on the timing and amount of a spill,
prevailing ocean currents and
conditions, and locations of ashy stormpetrels at the time of a spill. Similarly,
the threats of plastic ingestion and
organochlorine contaminants may occur
in both the northern and southern
portions of the ashy storm-petrel’s
range, but these threats are not
considered to be significant anywhere
within the species’ range.
Therefore, based on the analysis
above, we conclude that neither the
ashy storm-petrels on the Southeast
Farallon Island or the Channel Islands
are in danger of extinction (the second
step in determining whether an area is
a significant portion of the range),
because there is not substantial
information to suggest that the ashy
storm-petrel in either portion may
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become an endangered species within
the foreseeable future.
We request that you submit any new
information concerning the status of, or
threats to, the ashy storm-petrel to the
address listed in the ADDRESSES section
of this notice whenever it becomes
available. New information will help us
monitor this species and encourage its
conservation. If an emergency situation
develops for this species or any other
species, we will act to provide
immediate protection.
References Cited
A complete list of all references cited
herein is available, upon request, from
the Arcata Fish and Wildlife Office (see
ADDRESSES).
Author
The primary authors of this notice are
the staff of the Arcata Fish and Wildlife
Office (see ADDRESSES).
Authority
The authority for this action is section
4 of the Endangered Species Act of
1973, as amended (16 U.S.C. 1531 et
seq.).
Dated: August 11, 2009.
Rowan W. Gould,
Acting Director, U.S. Fish and Wildlife
Service.
[FR Doc. E9–19700 Filed 8–18–09; 8:45 am]
BILLING CODE 4310–55–S
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Agencies
[Federal Register Volume 74, Number 159 (Wednesday, August 19, 2009)]
[Proposed Rules]
[Pages 41832-41860]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E9-19700]
=======================================================================
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DEPARTMENT OF THE INTERIOR
Fish and Wildlife Service
50 CFR Part 17
[FWS-R8-ES-2008-0049;1111 FY08 MO-B2]
Endangered and Threatened Wildlife and Plants; 12-Month Finding
on a Petition To List the Ashy Storm-Petrel as Threatened or Endangered
AGENCY: Fish and Wildlife Service, Interior.
ACTION: Notice of 12-month petition finding.
-----------------------------------------------------------------------
SUMMARY: We, the U.S. Fish and Wildlife Service (Service), announce a
12-month finding on a petition to list the ashy storm-petrel
(Oceanodroma homochroa) as threatened or endangered, under the
Endangered Species Act of 1973, as amended (Act). After a thorough
review of all available scientific and commercial information, we find
that listing the ashy storm-petrel is not warranted. We ask the public
to continue to submit to us any new information concerning the status
of, and threats to, this species. This information will help us to
monitor and encourage the conservation of this species.
DATES: The finding announced in the document was made on August 19,
2009.
ADDRESSES: This finding is available on the Internet at https://www.regulations.gov and https://www.fws.gov/arcata/. Supporting
documentation we used in preparing this finding is available for public
inspection, by appointment, during normal business hours at the U.S.
Fish and Wildlife Service, Arcata Fish and Wildlife Office, 1655
Heindon Road, Arcata, CA 95521; telephone 707-822-7201; facsimile 707-
822-8411. Please submit any new information, materials, comments, or
questions concerning this finding to the above address.
FOR FURTHER INFORMATION CONTACT: Randy Brown, (Acting) Field
[[Page 41833]]
Supervisor, U.S. Fish and Wildlife Service, Arcata Fish and Wildlife
Office (see ADDRESSES section). If you use a telecommunications device
for the deaf (TDD), call the Federal Information Relay Service (FIRS)
at 1-800-877-8339.
SUPPLEMENTARY INFORMATION:
Background
Section 4(b)(3)(B) of the Act (16 U.S.C. 1531 et seq.) requires
that, for any petition to revise the Lists of Endangered and Threatened
Wildlife and Plants that contains substantial scientific and commercial
information that listing may be warranted, we make a finding within 12
months of the date of our receipt of the petition on whether the
petitioned action is: (a) Not warranted, (b) warranted, or (c)
warranted, but the immediate proposal of a regulation implementing the
petitioned action is precluded by other pending proposals to determine
whether any species is threatened or endangered, and expeditious
progress is being made to add or remove qualified species from the
Lists of Endangered and Threatened Wildlife and Plants. Such 12-month
findings are to be published promptly in the Federal Register. Section
4(b)(3)(C) of the Act requires that we treat a petition for which the
requested action is found to be warranted but precluded as though
resubmitted on the date of such finding, and we must make a subsequent
finding within 12 months.
Previous Federal Actions
On October 16, 2007, we received a petition, dated October 15,
2007, from the Center for Biological Diversity (CBD or petitioner),
requesting that we list the ashy storm-petrel as a threatened or
endangered species throughout its range and that we concurrently
designate critical habitat (CBD 2007, pp. 1-51). In response to the
petition, we sent a letter to the petitioner dated January 11, 2008,
stating that we had secured funding and that we anticipated making an
initial finding as to whether the petition contained substantial
information indicating listing the ashy storm-petrel may be warranted
in Fiscal Year 2008. We also concluded in our January 11, 2008, letter
that emergency listing of the ashy storm-petrel was not warranted. On
May 15, 2008, we published a 90-day petition finding (73 FR 28080) in
which we concluded that the petition provided substantial information
indicating that listing of the ashy storm-petrel may be warranted, and
we initiated a status review. This notice constitutes the 12-month
finding on the petition, dated October 15, 2007, to list the ashy
storm-petrel as threatened or endangered.
Species Description
The ashy storm-petrel is a seabird species belonging to the order
Procellariiformes, family Hydrobatidae. The ashy storm-petrel is one of
five storm-petrel species (including fork-tailed (Oceanodroma furcata),
Leach's (O. leucorhoa), black (O. melania), and least (O. microsoma)
storm-petrels) that nest on islands along the west coast of North
America (Harrison 1983, pp. 272-278). The ashy storm-petrel is a smoke-
gray, medium-sized bird with long slender wings, a long forked tail,
and webbed feet (Ainley 1995, p. 2).
Ashy storm-petrels have been confirmed to breed at 26 locations (on
islands and offshore rocks) from Mendocino County, California, south to
Todos Santos Islands, west of Ensenada, Baja California, Mexico (Carter
et al. 1992, pp. 77-81; Ainley 1995, p. 2; Carter et al. 2006, p. 6;
Carter et al. 2008a, p. 118). Greater than 95 percent of the species
breeds in two population centers at the Farallon Islands and in the
California Channel Islands (Sowls et al. 1980, p. 24; Ainley et al.
1990, p. 135; Carter et al. 1992, p. 86). Anacapa, San Miguel, Santa
Cruz, Santa Rosa, San Clemente, San Nicholas, Santa Barbara, and Santa
Catalina islands comprise the Channel Islands.
Ashy storm-petrels occur at their breeding colonies nearly year-
round and occur in greater numbers from February through October
(Ainley 1995, p. 5). Like other procellariids, ashy storm-petrels are
highly philopatric; that is, birds usually return in consecutive years
to the same breeding site or colony from which they were raised as
chicks (James-Veitch 1970, p. 81; Warham 1990, p. 12). Ashy storm-
petrels do not excavate burrows; rather, they nest in crevices of talus
slopes, rock walls, sea caves, cliffs, and driftwood (James-Veitch
1970, pp. 87-88; Ainley et al. 1990, p. 147; McIver 2002, p. 1). The
breeding season is protracted, and breeding activities (courtship, egg-
laying, chick-rearing) at nesting locations occur from February through
January of the following year (James-Veitch 1970, p. 71, Ainley et al.
1974, p. 301). During the pre-egg period, adult ashy storm-petrels
begin to visit nesting sites in February (Ainley et al. 1974, p. 301;
Ainley 1995, p. 5). Throughout the fledging period, the number of
visiting adults declines (Ainley et al. 1974, p. 301). At Southeast
Farallon Island, Ainley et al. (1974, p. 301) reported that immature
(non-breeding) ashy storm-petrels visited the island from April through
early July. The egg-laying period extends from late April to October,
peaking in June and July (James-Veitch 1970, p. 243; Ainley et al.
1990, p. 148; McIver 2002, p. 17). Clutch size is one egg per year, and
parents alternate incubation bouts during a 44-day incubation period
(James-Veitch 1970, p. 244; Ainley 1995, p. 6). Less than about 4
percent of all eggs laid are replacement (or re-lay) eggs, laid after
the failure of a first egg (Ainley et al. 1990, p. 148; McIver 2002, p.
18). Hatchlings are ``semi-precocial'' (James-Veitch 1970, p. 128). The
term semi-precocial describes young that have characteristics of
precocial young at hatching (open eyes, downy, capacity to leave the
nest), but that remain at the nest and are cared for by parents until
close to adult size (Sibley 2001, p. 573). Once hatched, the nestling
is brooded for about 5 days, after which it remains alone in the nest
site for an additional 75 to 85 days (James-Veitch 1970, pp. 141, 212;
Ainley et al. 1990, p. 152). It is fed irregularly (1 to 3 nights on
average) during brief, nocturnal visits by its parents from feeding
areas at sea (James-Veitch 1970, pp. 180-208). Fledging occurs at
night, from late August to January, and once they leave the nest,
fledglings are independent of their parents (Ainley et al. 1974, p.
303; McIver 2002, p. 36). Peak fledging occurs in early to mid-October
(McIver 2002, p. 18).
The nocturnal activity (return to and departure from nest) and
crevice nesting of the ashy storm-petrel are believed to be adaptations
to avoid predation by diurnal predators, such as western gulls (Larus
occidentalis), peregrine falcons (Falco peregrinus), and common ravens
(Corvus corax) (Ainley 1995, p. 5; McIver and Carter 2006, p. 3). Ashy
storm-petrels are susceptible to predation at night by burrowing owls
(Athene cunicularia) and barn owls (Tyto alba) (Ainley 1995, p. 5;
McIver 2002, p. 30). Nesting in crevices and burrows on remote
headlands, offshore rocks, and islands generally reduces predation of
storm-petrels by mammalian predators (Warham 1990, p. 13). Known
mammalian predators of ashy storm-petrels and their eggs include house
mice (Mus musculus), deer mice (Peromyscus maniculatus), and island
spotted skunks (Spilogale gracilis amphiala) (Ainley et al. 1990, p.
146; McIver 2002, pp. 40-41; McIver and Carter 2006, p. 3).
Obtaining direct population counts of ashy storm-petrels is
difficult because the species often nests in deep, inaccessible
crevices (Carter et al. 1992, p. 77; Sydeman et al. 1998a, p. 438).
Techniques for estimating population size at breeding locations have
included counting crevices and applying correction factors to account
for burrow
[[Page 41834]]
occupancy, mark and recapture using mist nests, and direct observation
of nest sites. Estimates of breeding ashy storm-petrels for California
have ranged from 5,187 (Sowls et al. 1980, p. 25) to 7,209 (Carter et
al. 1992, p. I-87). Additional colony sites and larger ashy storm-
petrel numbers have been found at several locations in the Channel
Islands and along the mainland coast of California (Carter et al.
2008a, p. 119). Table 1 provides various estimates of numbers of
breeding ashy storm-petrels at 26 locations in California and Baja
California Norte, Mexico.
Table 1. Estimates of Numbers of Breeding Ashy Storm-Petrels at 26 locations in California (United States) and
Baja California Norte (Mexico).
----------------------------------------------------------------------------------------------------------------
Source for
Location Ownership or Estimated No. Breeding Birds
Management\a\ Breeding Birds Estimates\b\
----------------------------------------------------------------------------------------------------------------
1 Bird Rock near BLM 10 1,2,3
Greenwood,
Mendocino County
----------------------------------------------------------------------------------------------------------------
2 Caspar, near Point BLM 10 1,2,3
Cabrillo,
Mendocino County
----------------------------------------------------------------------------------------------------------------
3 Bird Rock, Marin NPS 10 4
County
----------------------------------------------------------------------------------------------------------------
4 Stormy Stack, Marin NPS 10 4
County
----------------------------------------------------------------------------------------------------------------
5a Southeast Farallon FWS 4,000 5
Island
----------------------------------------------------------------------------------------------------------------
5b Southeast Farallon FWS 3,402 6
Island
----------------------------------------------------------------------------------------------------------------
5c Southeast Farallon FWS 1,990 6
Island
----------------------------------------------------------------------------------------------------------------
6 Castle/Hurricane BLM 60 7
Colony Complex,
Monterey County
----------------------------------------------------------------------------------------------------------------
7 Castle Rock, Santa USN/NPS 200 8
Barbara County
----------------------------------------------------------------------------------------------------------------
8 Prince Island USN/NPS 1,154 1
----------------------------------------------------------------------------------------------------------------
9 Shipwreck Cave, TNC/NPS 20 9
Santa Cruz Island
----------------------------------------------------------------------------------------------------------------
10 Dry Sandy Beach TNC/NPS 80 10,11,12,13
Cave, Santa Cruz
Island
----------------------------------------------------------------------------------------------------------------
11 Del Mar Rock, Santa NPS 10 1
Cruz Island
----------------------------------------------------------------------------------------------------------------
12 Cave of the Bird's TNC/NPS 52 10,11,12,13
Eggs, Santa Cruz
Island
----------------------------------------------------------------------------------------------------------------
13 Diablo Rocks, Santa NPS 20 8
Cruz Island
----------------------------------------------------------------------------------------------------------------
14 Orizaba (``Sppit'') NPS 40 10,11,12,13
Rock, Santa Cruz
Island
----------------------------------------------------------------------------------------------------------------
15 Bat Cave, Santa NPS 48 10,11,12,13
Cruz Island
----------------------------------------------------------------------------------------------------------------
16 Cavern Point Cove NPS 0 10,11,12,13
Caves, Santa Cruz
Island
----------------------------------------------------------------------------------------------------------------
17 Scorpion Rocks, NPS 140 1
Santa Cruz Island
----------------------------------------------------------------------------------------------------------------
18 Willows Anchorage NPS 111 1
Rocks, Santa Cruz
Island
----------------------------------------------------------------------------------------------------------------
19 Gull Island NPS 2 8
----------------------------------------------------------------------------------------------------------------
20 Santa Barbara NPS 874 1
Island
----------------------------------------------------------------------------------------------------------------
21 Sutil Island NPS 586 1
----------------------------------------------------------------------------------------------------------------
22 Shag Rock NPS 10 13
----------------------------------------------------------------------------------------------------------------
23 Ship Rock, Santa BLM 2 14
Catalina Island
----------------------------------------------------------------------------------------------------------------
24 Seal Cove Area, San BLM 10 15
Clemente Island
----------------------------------------------------------------------------------------------------------------
25 Islas Los MX 100 16
Coronados, Mexico
----------------------------------------------------------------------------------------------------------------
26 Islas Todos Santos, MX 10 17
Mexico
----------------------------------------------------------------------------------------------------------------
Total, if using 7,569 ..................
line 5a
----------------------------------------------------------------------------------------------------------------
Total, if using 6,971 ..................
line 5b
----------------------------------------------------------------------------------------------------------------
Total, if using 5,559 ..................
line 5c
----------------------------------------------------------------------------------------------------------------
\a\Entity listed once if same for both ownership and management, as follows: Bureau of Land Management (BLM);
Mexican Government (MX); National Park Service (NPS); The Nature Conservancy (TNC); U.S. Fish and Wildlife
Service (FWS); and U.S. Navy (USN).
[[Page 41835]]
\b\Sources are as follows: 1-Carter et al. 1992; 2-Carter et al. 2008a; 3-Carter et al. unpublished notes; 4-
Whitworth et al. 2002; 5-Ainley and Lewis 1974; 6-Sydeman et al. 1998a; 7-McChesney et al. 2000; 8-Hunt et al.
1979; 9-H. Carter, unpublished data; 10-McIver 2002; 11-McIver and Carter 2006; 12-Carter et al. 2007; 13-
McIver et al. 2008; 14-FWS estimate, based on Carter et al. 2008a; 15-H. Carter and D. Whitworth, unpublished
data; 16-Carter et al. 2006a; and 17-Carter et al 2006b.
Four thousand to six thousand ashy storm-petrels are usually
observed in the fall in Monterey Bay, approximately 3 to 10 miles (mi)
(5 to 16 kilometers (km)) offshore from the town of Moss Landing,
California. As many as 10,000 ashy storm-petrels were estimated to be
present in Monterey Bay in October 1977 and in September 2008 (Roberson
1985, p. 42; Shearwater Journeys 2008). However, both of these
estimates were from non-standardized visual estimates.
Spear and Ainley (2007, p. 27) examined the seasonal at-sea
distributions and abundance of storm-petrel species (including ashy
storm-petrels) with generalized additive models, and estimated 4,207
and 7,287 birds during autumn and spring, respectively (95 percent
confidence interval: 2,700 to 6,400 in autumn and 4,500 to 9,070 in
spring) off of Sonoma to Monterey counties. Spear and Ainley (2007, p.
7) suggested that higher numbers of ashy storm-petrels may occur at
Southeast Farallon Island, and other of the Farallon Islands, than have
previously been reported. The total population of ashy storm-petrels
(including breeders and non-breeders) has been estimated to be
approximately 10,000 birds (Sowls et al. 1980, p. 24; Ainley 1995,
p.1). Based on estimates at breeding locations and at-sea observations
in Monterey Bay and off Sonoma to Monterey counties, we consider 7,000
to 10,000 birds to be a reasonable estimate of the total population
size of ashy storm-petrels. However, based on other visual estimates
mentioned above, the total population could be as high as 13,000 birds.
More ashy storm-petrels breed at Southeast Farallon Island than at
any other single location (Sowls et al. 1980, p. 24; Carter et al.
1992, p. I-78). Assessing population size and trends has been done
through capture-recapture techniques using audio playback and mist nets
(see Ainley and Lewis 1974, p. 435; Sydeman et al. 1998a, p. 438).
Ainley and Lewis (1974, pp. 432-435) estimated 4,000 breeding ashy
storm-petrels at Southeast Farallon Island in years 1971 to 1972, from
birds captured and recaptured in mist nets at night. Sydeman et al.
(1998a, p. 438-442) re-analyzed data from Southeast Farallon Island for
years 1971 and 1972 (Ainley and Lewis 1974) and included data from year
1992 to estimate 6,461 total ashy storm-petrels and 3,402 breeding ashy
storm-petrels in 1971 to 1972, and 4,284 total ashy storm-petrels and
1,990 breeding ashy storm-petrels in 1992. Based on comparison of these
data sets, Sydeman et al. (1998a, p. 442) suggested declines of 34
percent and 42 percent in the total population and breeding population
of ashy storm-petrels, respectively, at Southeast Farallon Island.
Sydeman et al. (1998a, pp. 445-446) reported that this decline occurred
in prime storm-petrel nesting habitat, and suggested that this decline
in population size at Southeast Farallon Island was due to, in part, an
increase in the predation rate on ashy storm-petrel adults and sub-
adults by western gulls and burrowing owls. We interpret these results
cautiously because they are based on two data points: one from 1972 and
one 20 years later from 1992. Sydeman et al. (1998b, pp. 1-74)
conducted a population viability assessment of ashy storm-petrels at
Southeast Farallon Island, quantitatively examining the effects of
predation on population decrease of ashy storm-petrels. Sydeman et al.
(1998b, pp. 1-2) estimated a 2.87 percent decline in the population of
ashy storm-petrels from 1972 to 1992 and hypothesized that removal of
western gull predation would produce a stable population. They also
stated, given current population parameters and predation rates, the
population of ashy storm-petrels faces a high probability of quasi-
extinction within 50 years (Sydeman et al. 1998b, p. 2). Since 1992,
capture-recapture of ashy storm-petrels at Southeast Farallon Island
has continued and techniques have been further standardized (McChesney
2008, p. 4). Using data from 1999 to 2007, Warzybok and Bradley (2007,
p. 17) describe analysis of capture-recapture data that shows
increasing capture rates and increasing survival of ashy storm-petrels.
Specifically, they report the mean standardized capture rate (number of
birds caught per hour of effort) increased from approximately 13 birds
per hour to 38 birds per hour between 1999 and 2005 but declined
slightly in 2006. The mean capture rate for 2007 was 39 birds per hour
(Warzybok and Bradley 2007, p. 17). The authors also note that there
were a greater number of occupied nesting sites than in previous years.
Although there are caveats associated with Warzybok and Bradley's
(2007) analysis (See Factor C: Disease and Predation section below),
their report represents the best available information to date and
suggests an increasing population of ashy storm-petrels.
Research on reproductive success (or productivity, defined as
number of fledged chicks per adult pair) of the ashy storm-petrel has
been conducted only at Southeast Farallon Island (James-Veitch 1970,
pp. 1-366; Ainley et al. 1990, pp. 128-162; Sydeman et al. 1998a, pp.
1-74; PRBO Conservation Science,) and Santa Cruz Island (McIver 2002,
pp. 1-70; McIver and Carter 2006, pp. 1-6; Carter et al. 2007, pp. 1-
32; McIver et al. 2008, pp. 1-23; McIver et al. 2009, pp. 1-30; McIver
et al., in preparation, pp. 1-23). Reported productivity values are
presented in Table 2.
Table 2. Average values for productivity (fledged chicks per adult pair) of ashy storm-petrels at Southeast
Farallon Island and Santa Cruz Island, California, for several studies during 1964-1966 and 1971-2008. Sample
sizes are shown in parentheses.
----------------------------------------------------------------------------------------------------------------
Location Productivity Years Source
----------------------------------------------------------------------------------------------------------------
Southeast Farallon Island 0.42\a\(n = 184) 1964-1966 James-Veitch (1970)
----------------------------------------------------------------------------------------------------------------
Southeast Farallon Island 0.69(n = 356) 1972-1983\b\ Ainley and Boekelheide
(1990)
----------------------------------------------------------------------------------------------------------------
Southeast Farallon Island 0.74\d\(n = 540) 1971-1992\b\ Sydeman et al. (1998b)
----------------------------------------------------------------------------------------------------------------
Southeast Farallon Island 0.54\c\(n = 283) 1996-2007\e\ PRBO Conservation
Science unpublished
data; Warzybok and
Bradley (2007)
----------------------------------------------------------------------------------------------------------------
[[Page 41836]]
Santa Cruz Island 0.55(n = 477) 1995-1998 McIver et al. in
preparation, Table 4
----------------------------------------------------------------------------------------------------------------
Santa Cruz Island 0.65(n = 293) 2005-2008 McIver et al. in
preparation, Table 4;
McIver et al. (2009)
----------------------------------------------------------------------------------------------------------------
\a\Researcher disturbance (daily nest checks) negatively affected productivity.
\b\Excludes year 1977, when researcher disturbance negatively affected productivity.
\c\Sample sizes not provided for year 1996-2005, so annual sample size during this time period. assumed at 22
nests, based on average sample size in Sydeman et al. (1998b).
\d\Based on two data points.
\e\Based on yearly date.
No data are currently available regarding adult life span,
survivorship, and age at first breeding for ashy storm-petrels (Ainley
1995, p. 8). However, like other procellariids, storm-petrels are long-
lived (Warham 1996, p. 20). Some ashy storm-petrels reach 25 years old
(Sydeman et al. 1998b, p. 7), and breeding adults over 20 years in age
have been reported in the closely related Leach's storm-petrel (Morse
and Bucheister 1977, p. 344). Mean age of first breeding in the Leach's
storm-petrel has been reported at 5.9 years 1.3 years
(Huntington et al. 1996, p. 19). Sydeman et al. (1998b, p. 7) concluded
that 90 percent of adult ashy storm-petrels were capable of breeding at
6 years of age.
Marine Environment
Ashy storm-petrels are not as migratory as other storm-petrel
species, foraging primarily in the California Current, from northern
California to central Baja California, Mexico; the birds forage in
areas of upwelling, seaward of the continental shelf, near islands and
the coast (Ainley et al. 1974, p. 300; Briggs et al. 1987, p. 23; Mason
et al. 2007, p. 60). The California Current flows along the west coast
of North America, and like three other major, global, eastern boundary
(along the eastern edges of oceanic gyres and the western edges of
continents) currents, is characterized by the upwelling of cool,
nutrient-rich waters, which results in increased productivity of the
ocean (i.e., production of phytoplankton and zooplankton) in the region
(Hickey 1993, pp. 19-70). The California Current extends about 190 mi
(300 km) offshore from southern British Columbia, Canada, to Baja
California, Mexico, and is comprised of a southward surface current,
and a northward (poleward) undercurrent and surface countercurrents
(Miller et al. 1999, p. 1; Dailey et al. 1993, pp. 8-10). Upwelling is
an oceanographic phenomenon that involves wind-driven motion of dense,
cooler, and usually nutrient-rich water towards the ocean surface,
which replaces the warmer and usually nutrient-depleted surface water
(Smith 1983, pp. 1-2). Coastal upwelling replenishes nutrients in the
euphotic zone (zone of water where photosynthesis occurs), resulting in
increased productivity in higher trophic levels (position within the
food chain) (Batchelder et al. 2002, p. 37).
Crossin (1974, p. 176) observed ashy storm-petrels as far north as
latitude 49[deg] N, as far south as latitude 7[deg] S, and
approximately 300 mi (480 km) from shore near latitude 14[deg] N.
However, Spear and Ainley (2007, p. 7) disputed these observations and
state that these observations likely represented misidentified dark-
rumped Leach's storm-petrels. At-sea observations of ashy storm-petrels
south of Islas San Benitos, Mexico (latitude 28[deg] N) are unusual,
and most observations of the species are off the coasts of California
and Baja California Norte, Mexico (Briggs et al. 1987, p. 23; Ainley
1995, p. 2). Aerial and boat observations at-sea confirm that the
species is associated with pelagic (offshore) waters along the slope of
and just seaward of the Continental Shelf and the Monterey Submarine
Canyon, and less often in neritic (nearshore) waters (Briggs et al.
1987, p. 23; Mason et al. 2007, pp. 56-60; Adams and Takekawa 2008, pp.
12-13). Ashy storm-petrels are not known to be associated with the
deeper and warmer oceanic waters west of the California Current, unlike
the closely-related Leach's storm-petrel (Ainley et al. 1974, pp. 299-
300). Thus, the Service considers the at-sea geographic distribution
(i.e., marine range) of the ashy storm-petrel to include waters off the
western coast of North America, from latitude 42[deg] N (approximately
the California-Oregon State line) south to latitude 28[deg] N
(approximately Islas San Benitos, Mexico), and approximately 75 mi (120
km) out to sea from mainland and island coasts. The diet of ashy storm-
petrels has not been extensively studied, but likely includes
euphausiids (Euphausia spp., Thysanoessa), other crustaceans, larval
lanternfish, unidentified fish, fish eggs, and squid (Warham 1990, p.
186; McChesney 1999, pers. com.; Adams and Takekawa 2008, p. 14).
Summary of Factors Affecting the Species
Section 4 of the Act (16 U.S.C. 1533) and implementing regulations
at 50 CFR part 424 set forth procedures for adding species to the
Federal List of Endangered and Threatened Wildlife. In making this
finding, we summarize below information regarding the status and
threats to this species in relation to the five factors in section
4(a)(1) of the Act. In our 90-day finding for this petition (73 FR
28080), we organized potential threats under the five factors according
to how they were organized and described in the petition. In this 12-
month finding, we analyze all of the potential threats described in the
petition, but have reorganized them slightly under the factors that
more appropriately categorize them. In making our 12-month finding, we
considered and evaluated all scientific and commercial information
available, including information received during and after the public
comment period that ended July 14, 2008.
Factor A: The Present or Threatened Destruction, Modification, or
Curtailment of the Species' Habitat or Range
Like most other procellariids, ashy storm-petrels feed mostly
offshore or pelagically (Warham 1990, p. 10; Ainley 1995, p. 2) and
return to land to breed at locations on islands and offshore rocks
protected from mammalian predators (Warham 1990, p. 13; Ainley 1995, p.
3). Consequently, in this section, we describe various threats that may
destroy, modify, or curtail the ashy storm-petrel's marine and
terrestrial habitats and range. The petitioner asserts that the ashy
storm-petrel is
[[Page 41837]]
being or will be negatively affected by current and future climate
change (specific effects: reduction in ocean productivity; ocean
acidification; and sea level rise), tourism (specific effects:
disturbance of habitats and nesting birds), and introduced grasses (CBD
2007, p. 15). The petitioner further asserts that the ashy storm-
petrel's at-sea foraging habitat is being degraded by artificial
(human-caused) light pollution, chemical and plastics pollution, and
current and future oceanic changes related to climate change resulting
from greenhouse gas emissions (CBD, p. 15); We addresspotential threats
posed by artificial light pollution and chemical and plastics pollution
under Factor E below. In this 12-month finding, we discuss under Factor
A the following potential threats: (1) Climate change and associated
effects--specifically, reduced productivity, ocean acidification, and
sea-level rise; (2) introduced grasses; and (3) degradation of nesting
habitats from tourism and military operations. The petitioner states
that global warming will likely affect the ashy storm-petrel by causing
warmer water and reduced upwelling, which reduces primary productivity
in the California current system that would in turn decrease ashy
storm-petrel breeding success and perhaps survival; global warming is
leading to more intense El Ni[ntilde]o events that could lead to ashy
storm-petrel breeding failures; sea-level rise will eliminate important
ashy storm-petrel breeding habitat in sea caves and off-shore rocks in
the Channel Islands; and ocean acidification may lead to declines in
the prey species upon which petrels depend (CBD 2007, p 2). We discuss
first below the various climate-related factors affecting ashy storm-
petrels.
El Ni[ntilde]o and Reduced Productivity
The term El Ni[ntilde]o-Southern Oscillation (hereafter, El
Ni[ntilde]o) is used to describe periodic basin-wide changes in air-sea
interaction in the equatorial Pacific Ocean region, which result in
increased sea-surface temperatures, reduced flow of eastern boundary
currents, and reduced coastal upwelling (Norton and McLain 1994, pp.
16,019-16,030; Schwing et al. 2002, p. 461). La Ni[ntilde]a events
(sometimes called anti-El Ni[ntilde]o or cold-water events) produce
effects in the northeast Pacific Ocean that tend to be the reverse of
those that occur during El Ni[ntilde]o events; during La Ni[ntilde]a
events, strong upwelling-favorable winds and a shallow thermocline
(zone of rapid temperature change with increased depth that typically
separates warm and cold water) result in colder, more nutrient-rich
waters than usual (Murphree and Reynolds 1995, p. 52; Oedekoven et al.
2001, p. 266). In addition to inter-annual climate events such as El
Ni[ntilde]o and La Ni[ntilde]a, the mid-latitude Pacific Ocean
experiences warm and cool phases that occur on decadal time scales
(Mantua 2000, p. 2). The term ``Pacific Decadal Oscillation'' was
coined to describe long-term climate variability in the Pacific Ocean,
in which there are observed warm and cool phases, or ``regime shifts''
(Mantua et al. 1997, pp. 1069-1079).
The California Current system is affected by inter-annual (ENSO-
related (El Ni[ntilde]o/La Ni[ntilde]a)) and inter-decadal (Pacific
Decadal Oscillation) climatic processes. The petitioner cites
Behrenfeld et al. (2006, pp. 752-755) to describe significant global
declines in net primary production between years 1997 and 2005,
attributed to reduced nutrient enhancement due to ocean surface warming
(CBD 2007, p. 25). Specific to the marine range of the ashy storm-
petrel, the petitioner states that the California Current System has
experienced some of the most well-documented changes in ocean climate
due to global warming (CBD 2007, p. 25). The petition cites several
examples of changes in the California Current System, which it
attributes to climate change, that all relate to reduced ocean
productivity, including: reduction in zooplankton biomass and increased
sea surface temperatures (Roemmich and McGowan 1995, pp. 1324-1326;
Lynn et al. 1998, pp. 25-49); upwelling of warmer, nutrient-depleted
waters, which leads to breeding failures, mortality, and population
declines across trophic levels (Barber and Chavez 1983, pp. 1203-1210);
delay in the onset of spring upwelling (Schwing et al. 2006, pp. 1-5);
anomalously warm water, low nutrient levels, and low primary production
(Thomas and Brickley 2006, pp. 1-5); reduced zooplankton biomass
(Mackas et al. 2006, pp. 1-7); unprecedented seabird breeding failures
(Sydeman et al. 2006, pp. 1-5); and anomalously low recruitment of
rocky intertidal organisms (Barth et al. 2007, pp. 3719-3724). Specific
changes in the California Current that may negatively affect the ashy
storm-petrel are discussed below.
Roemmich and McGowan (1995, pp. 1324-1326) described 43 years (from
1951 to 1993) of observations off the southern California coast. They
reported that zooplankton had decreased by 80 percent, and that surface
temperatures taken during transects off Point Conception and Orange
County (approximately) warmed by an average of 2.2 [deg]F (1.2 [deg]C)
and 2.3 [deg]F (1.6 [deg]C), respectively, during this period. They
suggested that the zooplankton decline was directly related to and
caused by the observed warming (Roemmich and McGowan 1995, p. 1325).
The petitioner cited Schwing et al. (2006, pp. 1-5), Barth et al.
(2007, pp. 3719-3724), and Sydeman et al. (2006, pp. 1-5) to describe a
delay in the onset of spring upwelling in the northern California
Current that resulted in breeding failures of Cassin's auklets
(Ptychoramphus aleuticus) at Southeast Farallon Island, and at Triangle
Island, British Columbia, in 2005 (CBD 2007, p. 25). At Southeast
Farallon Island, Cassin's auklets also failed to breed in 2006 as well,
likely as a result of warm-water conditions, reduced upwelling, and
reduced availability of krill (Warzybok et al. 2006, pp. 12-14).
At Southeast Farallon Island, productivity (chicks fledged per
breeding pair) of ashy storm-petrels was 0.56 in 2005, and 0.48 in 2006
(Warzybok et al. 2006, p. 7). At Santa Cruz Island, productivity of
ashy storm-petrels was 0.58 in 2005, and 0.68 in 2006 (McIver et al. in
preparation, tables 2-4). Sydeman et al. (2006, p. 1) reported that
euphausiid crustacean (krill) biomass in the Gulf of the Farallones was
reduced in 2005, but remained high south of Point Conception. To
successfully raise a chick, an adult storm-petrel must obtain enough
food for itself, plus one-half the food requirements of the chick, plus
food to fuel the metabolic costs of transporting food to the nesting
location (Quinlan 1979, p. 103). Thus, if food was less available to
ashy storm-petrels foraging north of Point Conception (presumably,
Southeast Farallon Island breeders) in 2005 and 2006, adverse affects
may have appeared during the chick stage, and this could explain (in
part) reduced breeding success at Southeast Farallon Island in 2006.
Like Cassin's auklets, ashy storm-petrels feed on krill. However,
unlike Cassin's auklets, ashy storm-petrels have more extended
incubation and chick-rearing periods (per egg-laying effort), and feed
over a wider geographic area; thus, they are likely more able to
exploit similar food resources when these resources are reduced or more
patchily distributed. As stated earlier, Cassin's auklets failed to
breed in 2005 and 2006, in contrast to ashy storm-petrels, which did
breed. Additionally, Ainley (1990b, pp. 357-359) reported that ashy
storm-petrels showed the lowest inter-annual variability in
productivity of any species breeding at Southeast Farallon Island, for
the years 1971 to 1983. Ashy storm-petrel productivity was 0.64 and
0.69 in 1972
[[Page 41838]]
(n = 36) and 1973 (n = 35), respectively; 0.81 in 1976 (n = 37); and
0.75 and 0.67 in 1982 (n = 28) and 1983 (n = 18), respectively (Ainley
and Boekelheide 1990, p. 392). This is of importance because during
this time period, El Ni[ntilde]o events occurred in 1972-73, 1976, and
1982-83 (Ainley 1990a, p. 36). Ainley (1990b, p. 371) reported that
breeding by other seabirds at Southeast Farallon Island was poor to
nonexistent in 1973, 1976, 1978, 1982, and 1983. As noted above, ashy
storm-petrels were the exception to this observation; they bred in all
years of the study, and no clear correlation between warm-water years
and reduced reproductive success (productivity) was evident for this
species (Ainley and Boekelheide 1990, p. 392). The only response to El
Ni[ntilde]o conditions that may be evident are smaller numbers of ashy
storm-petrels breeding and delayed egglaying (later in the season than
in other years) (Ainley and Boekelheide 1990, p. 392; Ainley et al
1990, pp. 149-150). However, since regular annual monitoring of nesting
activities began at Southeast Farallon Island (in 1971) and at Santa
Cruz Island (in 1994), researchers have observed ashy storm-petrels (on
a population level) breeding each year. In research conducted in 1995-
97 and 2005-07, McIver et al. (in preparation, p. 10) report that
reproductive success (productivity) of ashy storm-petrels at Santa Cruz
Island did not appear to be negatively affected by El Ni[ntilde]o
conditions (although timing of breeding was later in 1998, an El
Ni[ntilde]o year), and no clear relationship between oceanographic
conditions in southern California and reproductive success of ashy
storm-petrels was observed. As presented above, this is supported by
data from research at Southeast Farallon Island. Productivity of ashy
storm-petrels at Southeast Farallon Island declined from the late 1980s
to the mid-1990s (Sydeman et al. 2001, p. 315; CBD 2007, p. 8; Warzybok
and Bradley 2007, p. 7). However, more recent data indicate that this
decline in productivity has not continued. Warzybok and Bradley (2007,
p. 17) describe an analysis of capture-recapture data that shows
increasing capture rates and increasing survival of ashy storm-petrels
on Southeast Farallon Island. Based on observed annual breeding and
reproductive success values of ashy storm-petrels during El Ni[ntilde]o
events, and the low inter-annual variability in reproductive success as
reported by Ainley and Boekelheide (1990, p. 392) and McIver (2002, p.
29), we conclude there is no clear relationship between reduced
productivity of phytoplankton and zooplankton in the California Current
due to El Ni[ntilde]o events and reproductive success of ashy storm-
petrels.
As enumerated above, the petition cited several examples of changes
in the California Current System, revolving around ocean productivity,
which the petition claims has had an adverse effect on ashy storm-
petrels. Based on our review of the available information, we found
that some species of seabirds have experienced breeding failures in
certain years, which can be linked to El Ni[ntilde]o events, warmer
water, or lower primary productivity. However, productivity of the ashy
storm-petrel over approximately the past 40 years does not show
breeding failures in those same years. This is likely due to the
species' ability to exploit a wider range of resources than other
seabirds. Based on the species' response to El Ni[ntilde]o events, we
conclude the ashy storm-petrel is not likely to be adversely affected
by potentially lower ocean productivity due to long-term ocean warming.
In 2006, when Cassin's auklets failed to breed at Southeast Farallon
Island likely as a result of warm-water conditions, reduced upwelling,
and reduced availability of krill or a delay in the onset of spring
upwelling, ashy storm-petrels did breed but had slightly lower
productivity. Based on this information, we do not consider the delay
in the onset of spring upwelling to be a threat to the species.
Therefore, based on the best scientific information available to the
Service regarding the effects of climate change, including the effects
of El Ni[ntilde]o and changes in the California Current on ocean
productivity, we do not consider this to be a significant threat to the
ashy storm-petrel at Southeast Farallon Island, at the Channel Islands,
or rangewide.
Climate Change - Ocean Acidification
The petitioner claims that ocean acidification may eventually have
detrimental impacts on the ashy storm-petrel's crustacean prey species
(e.g., Euphausia pacifica, Thysannoessa spinifera) that may be impaired
in building their exoskeletons in the coming decades (CBD 2007, p. 29).
The petitioner cites Orr et al. (2005, p. 682) that mid-latitude
waters, where the California Current Ecosystem is located, are
experiencing the largest decreases in surface carbonate ion
concentrations.
The chemical processes behind ocean acidification are well known.
The presence of inorganic carbon in the ocean is largely responsible
for controlling the pH (the measure of acidity) of seawater, and
dissolved inorganic carbon in seawater exists in three major forms,
including a bicarbonate ion, carbonate ion, and aqueous carbon dioxide
(Fabry et al. 2008, pp. 414-415). Human industrial and land use
activities are resulting in increased atmospheric concentrations of
carbon dioxide (Feely et al. 2004, p. 362); much carbon dioxide is
absorbed by the oceans (Caldiera and Wickett 2003, p. 365; Sabine et
al. 2004, p. 370). When carbon dioxide dissolves in water, carbonic
acid is formed, most of which quickly dissociates into a hydrogen ion
and a bicarbonate ion; the hydrogen ion can further react with a
carbonate ion to form bicarbonate (Fabry et al. 2008, p. 415). The
effects of increased absorption of carbon dioxide by the oceans have
been given the term ``ocean acidification'' and include an increase in
concentrations of carbonic acid, bicarbonate, and hydrogen ions; a
decrease in concentration of carbonate; and a reduction in the pH level
in seawater (Caldiera and Wickett 2003, p. 365; Royal Society et al.
2005, p.16; Fabry et al. 2008, p. 415). Pure water has a pH of 7;
solutions below pH 7 are acidic, and solutions above pH 7 are alkaline,
or basic (summarized in Hardt and Safina 2008, p. 1). Oceans are
slightly alkaline, with a pH of 8.1 (at latitude 30[deg]N,
approximately; Caldiera and Wickett 2005, p. 5). Measurements of
surface ocean pH in 2005 were 0.1 unit lower than preindustrial values
(prior to the 1850s) and could become 0.3 to 0.4 units lower by the end
of the 21st century (Caldiera and Wickett 2005, p. 5). Marine organisms
that produce shells, such as corals, mollusks, echinoderms, and
crustaceans, require carbonate ions to produce their calcium carbonate
shells and skeletons (Orr et al. 2005, p. 681; Fabry et al. 2008, p.
415). There are three mineral forms of calcium carbonate (magnesium-
calcite, aragonite, and calcite), and each has different tendencies to
dissolve (solubility) in seawater (summarized in Hardt and Safina 2008,
p. 2). The reaction of excess carbon dioxide with seawater reduces the
availability of carbonate ions necessary for shell and skeleton
formation for these organisms (Fabry et al. 2008, p. 415). Generally,
oceanic surface waters are saturated with calcium carbonate, deeper
waters are under-saturated, and the depth where waters transition from
saturated to unsaturated is called the saturation horizon (summarized
in Hardt and Safina 2008, p. 2). A reduction in carbonate ions causes
all forms of calcium carbonate to dissolve at shallower depths, and
causes a reduction in the rate at which marine
[[Page 41839]]
organisms can produce calcium carbonate (summarized in Hardt and Safina
2008, p. 2). In other words, once formed, calcium carbonate will
dissolve back into the water unless the surrounding seawater contains
sufficiently high concentrations of carbonate ions (Royal Society et
al. 2005, p. 10).
The major planktonic calcium carbonate producers in the ocean are
coccolithophores (single-celled phytoplankton), foraminifera (amoeboid
protists), and pteropods (marine mollusks) (Fabry et al. 2008, p. 417).
Marine organisms act as a ``biological pump,'' removing carbon dioxide
and nutrients from the surface ocean and transferring these elements
into the deeper ocean and ocean bottom (Zondervan et al. 2001, p. 507;
Chen et al. 2004, p.18).
Feely et al. (2008, pp. 1490-1492) conducted hydrographic surveys
along the continental shelf of North America, and found evidence for
undersaturated (with respect to aragonite) and low pH (less than 7.75)
waters at mid-shelf depths of approximately 131 to 394 feet (ft) (40 to
120 meters (m)) from about middle California (latitude 37[deg] N,
approximately) to Baja California Sur, Mexico (latitude 26[deg] N,
approximately). Feely et al. (2008, p. 1492) reported that much of the
corrosive character of these waters is natural as the result of
respiration processes at intermediate depths below the euphotic zone.
Feely et al. (2008, p. 1492) cautioned that the California coastal
region continues to accumulate anthropogenic carbon dioxide, and
concluded that seasonal upwelling processes enhance the advancement of
the corrosive deep water into wide regions of the North American
continental shelf. Feely et al. (2008, p. 1492) further reported that
little was known about how intermittent exposure to acidified water
might affect the development of calcifying, or shell building,
organisms in this region.
The ecological effects of changing ocean carbonate chemistry are
uncertain due to complexities of marine ecosystems, and research to
date has focused on the impact of acidification on calcifying organisms
(Antarctic Climate & Ecosystems Cooperative Research Centre 2008, p.
7). Although the chemical processes associated with ocean acidification
and the biological processes involving the transport of carbon in the
oceans have been studied and described in detail, little research has
been conducted to assess the response of many zooplankton populations,
including euphausiids (upon which ashy storm-petrels likely feed), to
ocean acidification (Fabry et al. 2008, p. 426). However, the Service
is aware of one study (Yamada and Ikeda 1999, pp. 62-67) that
experimentally tested the acute (lethal) effects of lowered pH levels
upon Euphausia pacifica, a species of krill that occurs in the northern
Pacific Ocean and is a known prey item of ashy storm-petrels. Observing
5 juveniles and 20 nauplii (the free-swimming first stage of the larva)
of Euphausia pacifica, Yamada and Ikeda (1999, pp. 65) found increased
mortality with increased exposure time and decreased pH (less than
6.9). Based on their data, Yamada and Ikeda (1999, p. 66) also
suggested that the ability to tolerate lowered pH may be highly
variable between and possibly within species, as in the case of nauplii
and juveniles of Euphausia pacifica. Yamada and Ikeda (1999, p. 66)
suggested that information about pH levels that induce chronic
(sublethal) effects would be more appropriate to estimate the long-term
consequences for a given zooplankton population, in that zooplankton
may survive exposure to lower pH levels but may be unable to produce
normal offspring. The Service is also aware of research currently being
conducted to study the possible effects of ocean acidification on
euphausiids in waters near Antarctica (see Rowbotham 2008, p. 1), but
this research has just begun and data are currently not available (T.
Berli, personal communication 2008).
As stated in the Species Description section, the diet of ashy
storm-petrels has not been extensively studied; however, like other
species of storm-petrels, ashy storm-petrels likely feed on
euphausiids, juvenile lanternfish, fish eggs, and other small fish that
occur at the surface of the ocean. Our review of the available
information did not reveal any information regarding diet studies or
measurements of chick growth and weight that indicate that ashy storm-
petrels are eating fewer euphausiids or are providing less food to
their chicks. Additionally, our review of the available information did
not find any research indicating that ocean acidification is causing
acute or chronic effects to euphausiid populations that occur in the
California Current, or any other species of krill that occur in the
California Current, on which ashy storm-petrels feed. Although the
processes and potential effects of ocean acidification on biological
food webs have been described, and experimental research on Euphausia
pacifica has tested lethal effects of exposure to low pH, our review of
the available information did not reveal any evidence that demonstrates
a direct link between ocean acidification and reduced abundance and
survival of prey items on which ashy storm-petrels depend.
Additionally, Ainley (1990b, p. 371) reported that breeding by other
seabirds at Southeast Farallon Island was poor to nonexistent during
warm-water years (El Ni[ntilde]o events). However, ashy storm-petrels
bred in years that other seabird species did not (Ainley and
Boekelheide 1990, p. 392), which is an indication that the ashy storm-
petrel is less affected by changes in ocean productivity than other
species. Therefore, based on our review of the available information,
we conclude that the potential effects of ocean acidification are not
currently a significant threat to ashy storm-petrels based on the
uncertainty of the ecological effects of changing ocean carbonate
chemistry.
Published research and oceanographic modeling does show that oceans
are acidifying, and we recognize that ashy storm-petrels may be
susceptible to changes in the oceans' chemistry in the future. However,
based on the best scientific information available to the Service
regarding ocean acidification, at this time we do not consider ocean
acidification to be a significant threat to the ashy storm-petrel at
Southeast Farallon Island, at the Channel Islands, or rangewide.
Climate Change - Sea Level Rise
The petitioner claims that climate change will cause rises in the
elevation of the oceans that will have negative consequences for ashy
storm-petrels by eliminating (presumably, by inundation and submersion
by seawater) important habitat in sea caves and offshore rocks in the
California Channel Islands (CBD 2007, p. 28). Sea levels along the
California coast are projected to rise approximately 1 ft (0.3 m) by
2050 and approximately 3 ft (0.9 m) by 2100 (California Coastal
Commission 2001, pp. 14-15; Cayan et al. 2006, p. S71). Future sea
levels along the coast of California will likely depend upon (in part):
future changes in global temperatures; lag time between atmospheric
changes and oceanic reactions; thermal expansion of ocean water;
effects of atmospheric temperature changes on Antarctica; melting of
Greenland ice and other glaciers; and local subsidence and uplift of
coastal areas (California Coastal Commission 2001, p. 12). Gradual sea
level rises progressively worsen the impacts of high tides (through
erosion and submersion), surge, and waves resulting from storms (Cayan
et al. 2008, pp. S57-S58).
[[Page 41840]]
We reviewed topographic maps and information provided in Sowls et
al. (1980), Bunnell (1988), and Carter et al. (1992; 2006a; 2006b) to
estimate the range of elevations above sea level of suitable ashy
storm-petrel habitat at each of the 26 known breeding locations (Table
3).
Table 3. Estimated range of elevation above sea level (ASL) in feet (ft)
and meters (m) of known nesting habitat of ashy storm-petrels.
------------------------------------------------------------------------
Location Number Breeding Location Name Elevation ASL
------------------------------------------------------------------------
1............................. Bird Rock near 10-40 ft (3-12
Greenwood, Mendocino m)
County.
2............................. Caspar, near Point 10-40 ft (3-12
Cabrillo, Mendocino m)
County.
3............................. Bird Rock, Marin 10-40 ft (3-12
County. m)
4............................. Stormy Stack, Marin 10-50 ft (3-15
County. m)
5............................. Southeast Farallon 10-330 ft (3-100
Island. m)
6............................. Castle/Hurricane 10-100 ft (3-30
Colony Complex, m)
Monterey County.
7............................. Castle Rock, Santa 20-80 ft (6-24
Barbara County. m)
8............................. Prince Island......... 20-300 ft (6-91
m)
9............................. Shipwreck Cave, Santa 5-15 ft (1.5-5
Cruz Island. m)
10............................ Dry Sandy Beach Cave, 5-15 ft (1.5-5
Santa Cruz Island. m)
11............................ Del Mar Rock, Santa 5-20 ft (1.5-6
Cruz Island. m)
12............................ Cave of the Birds 5-10 ft (1.5-3
Eggs, Santa Cruz m)
Island.
13............................ Diablo Rocks, Santa 10-40 ft (3-12
Cruz Island. m)
14............................ Orizaba Rock, Santa 10-30 ft (3-9 m)
Cruz Island.
15............................ Bat Cave, Santa Cruz 5-20 ft (1.5-6
Island. m)
16............................ Cavern Point Cove 0-10 ft (0-3 m)
Caves, Santa Cruz
Island.
17............................ Scorpion Rocks, Santa 10-40 ft (3-12
Cruz Island. m)
18............................ Willow Anchorage 10-40 ft (3-12
Rocks, Santa Cruz m)
Island.
19............................ Gull Island, Santa 10-100 ft (3-30
Cruz Island. m)
20............................ Santa Barbara Island.. 10-600 ft (3-183
m)
21............................ Sutil Island.......... 10-250 ft (3-76
m)
22............................ Shag Rock............. 10-50 ft (3-15
m)
23............................ Ship Rock, Santa 5-20 ft (1.5-6
Catalina Island. m)
24............................ Seal Cove Area, San 10-50 ft (3-15
Clemente Island. m)
25............................ Islas Los Coronados, 10-100 ft (3-30
Mexico. m)
26............................ Islas Todos Santos, 10-100 ft (3-30
Mexico. m)
------------------------------------------------------------------------
The nesting habitat at the majority of ashy storm-petrel breeding
locations will likely not be affected by the sea level rise projected
for California by 2100 (Table 3). Some nesting habitat at only one
location at Cavern Point Cove Caves, Santa Cruz Island, would likely be
submerged if projected sea level rises of 1 ft (0.3 m) by 2050 occur;
much of the nesting habitat at this location would likely be submerged
if the sea level rises 3 ft (0.9 m) by year 2100. Prior to the
mortality event in 2008 at this location (see Factor C), Cavern Point
Cove Caves had approximately 40 breeding birds annually. Some habitat
at other cave locations on Santa Cruz Island may be susceptible to
submersion by seawater. For example, on Santa Cruz Island in November
2008, McIver et al. (2009, p. 6) reported flooding by ocean water in a
sea cave that likely killed one storm-petrel chick. Despite this
unusual event, the majority of the nesting habitat in the sea caves at
Santa Cruz Island occurs greater than 3 ft (1 m) above current sea
level, and would not likely be submerged during breeding season months
(April through November) within the next 40 to 50 years. Winter storm
surges periodically wash all of the sea caves at Santa Cruz Island, but
these storm events likely do not negatively affect ashy storm-petrels,
since most ashy storm-petrels are not attending the colonies during
winter months (Ainley 1995, p. 5). In fact, past winter storms have
benefited ashy storm-petrels at Santa Cruz Island by creating nesting
habitat; approximately 25 percent of ashy storm-petrel nest sites in
Bat Cave occur among accumulated driftwood debris (both human-made and
natural) that has washed into the cave during past winter storm events.
Based on information available to the Service regarding elevations
(above current sea level) of breeding locations of ashy storm-petrels,
and projected estimates of sea level rise along the west coast of North
America during the 21st century, we conclude that a small portion of
the total population of ashy storm-petrels (approximately 0.8 percent)
could be negatively affected by rising sea levels by 2050. Therefore,
based on the best scientific information available to the Service
regarding climate change-induced sea level rise, at this time we do not
consider this to be a significant threat to the ashy storm-petrel at
Southeast Farallon Island, at the Channel Islands, or rangewide.
Changes in Terrestrial Breeding Habitat
Introduced Grasses
The petitioner asserts that the ashy storm-petrel's island breeding
habitats are being modified and degraded by introduced species and
specifically, that introduced grasses have increased at Southeast
Farallon Island, causing some nesting areas to be unusable for ashy
storm-petrels (CBD 2007, p. 30). In addition, the petitioner claims
that introduced grasses are widespread at all ashy storm-petrel
colonies and that their effects have not been evaluated (CBD 2007, p.
30). Ainley (1995, p. 9) desc