Endangered and Threatened Wildlife and Plants; 12-Month Finding on a Petition To List the Yellow-Billed Loon as Threatened or Endangered, 12932-12968 [E9-6012]
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Federal Register / Vol. 74, No. 56 / Wednesday, March 25, 2009 / Proposed Rules
DEPARTMENT OF THE INTERIOR
Fish and Wildlife Service
50 CFR Part 17
[FWS–R7–ES–2009–0133; MO9221050083–
B2]
Endangered and Threatened Wildlife
and Plants; 12-Month Finding on a
Petition To List the Yellow-Billed Loon
as Threatened or Endangered
PWALKER on PROD1PC71 with PROPOSALS2
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 yellow-billed loon (Gavia adamsii)
as threatened or endangered, with
critical habitat, under the Endangered
Species Act of 1973, as amended (Act).
The petitioners provided two listing
options for consideration by the Service:
(1) Listing the yellow-billed loon
throughout its range, or (2) listing the
United States population of the yellowbilled loon as a Distinct Population
Segment (DPS). After a review of the
best available scientific and commercial
information, we have determined that
listing the yellow-billed loon rangewide
under the Act is warranted but
precluded by other higher priority
listing actions.
DATES: This finding was made on March
25, 2009.
ADDRESSES: This finding is available on
the Internet at https://
www.regulations.gov. Data, information,
comments, or questions regarding this
notice should be submitted to the Field
Supervisor, Endangered Species Branch,
Fairbanks Fish and Wildlife Field
Office, U.S. Fish and Wildlife Service,
101–12th Ave., Room 110, Fairbanks,
AK 99701. The complete administrative
file for this finding is available for
public inspection, by appointment,
during normal business hours at the
above address.
FOR FURTHER INFORMATION CONTACT: Mr.
Ted Swem, Fairbanks Fish and Wildlife
Field Office (see ADDRESSES) (telephone
907–456–0441; facsimile 907–456–
0208). If you use a telecommunications
device for the deaf (TDD), call the
Federal Information Relay Service
(FIRS) at 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 presenting substantial
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scientific and commercial information
that listing may be warranted, we make
a finding within 12 months of the date
of receipt of the petition on whether the
petitioned action is: (a) Not warranted,
(b) warranted, or (c) warranted, but that
immediate proposal of a regulation
implementing the petitioned action is
precluded by other pending proposals to
determine whether species are
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. 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 is, therefore, subject to a new
finding to be made within 12 months
and subsequently thereafter until we
take action on a proposal to list or
withdraw our original finding. We must
publish these 12-month findings in the
Federal Register.
Previous Federal Actions
On April 5, 2004, we received a
petition from the Center for Biological
Diversity (CBD) (Sitka, AK), Natural
Resources Defense Council
(Washington, DC), Pacific Environment
(San Francisco, CA), Trustees for Alaska
(Anchorage, AK), Kaira Club (Chukotka,
Anadyr, Russia), Kronotsky Nature
Preserve (Kamchatka Region, Russia),
Taiga Rangers (Khabarovsk Region,
Russia), Yuzhno-Sakhalinsk Local
Public Fund (Sakhalin Region, Russia),
Interregional Public Charitable
Organization of Far Eastern Resource
Centers (Vladivostok, Russia),
Kamchatka Branch of Pacific Institute of
Geography (Petropavlovsk-Kamchatsky,
Russia), and Kamchatka League of
Independent Experts (PetropavlovskKamchatsky, Russia) to list the yellowbilled loon as endangered or threatened
throughout its range, or as a Distinct
Population Segment in the United
States, and to designate critical habitat
once listed. The petition summarizes
threats to the species based on CBD’s
review of Fair’s (2002) report, prepared
for the Natural Resources Defense
Council and Trustees for Alaska, on the
status and significance of the species in
Alaska, as well as CBD’s review of the
scientific literature. In September 2006,
the Service completed a ‘‘Conservation
Agreement for the Yellow-billed Loon
(Gavia adamsii)’’ with Federal, State,
and local partners. In response to the
petition, we published a 90-day finding
on the yellow-billed loon in the Federal
Register on June 6, 2007 (72 FR 31256).
In the 90-day finding we determined
that the petition presented substantial
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scientific or commercial information to
indicate that a listing may be warranted
and announced that a status review
would be promptly commenced. In that
notice we announced the opening of a
60-day information collection period
and invited the public to submit to us
any pertinent information concerning
the status of or threats to this species.
Approximately 28,000 comments were
received during the information
collection period. We also consulted
with recognized yellow-billed loon
experts and other Federal and State
agencies. We sent letters to national
wildlife or natural resource agencies in
Canada, China, Japan, North Korea,
Norway, Republic of Korea (South
Korea), and the Russian Federation,
asking for information about ongoing
management measures and any
conservation and management strategies
being developed to protect the species.
We received a formal response from the
government of Canada, and an informal
response from a government biologist in
the Russian Federation.
On June 11, 2007, we received a 60day notice of intent to sue from the
Center for Biological Diversity alleging a
violation of section 4 of the ESA for
failure to complete a 12-month finding
on the petition. We informed the
plaintiffs by letter dated July 9, 2007,
that further action on the petition was
precluded by higher priority listing
actions but that, pending the fiscal year
2008 allocation of funds, we hoped to
complete the 12-month finding within
that fiscal year.
On December 19, 2007, the Center for
Biological Diversity (CBD) filed a
complaint alleging that the Service had
failed to make a timely 12-month
finding on the petition, as required
under section 4 of the ESA. Consistent
with a settlement agreement reached
between the Service and CBD, the Court
ordered the Service to submit this 12month finding for publication to the
Federal Register by February 15, 2009.
Because the Service later received
substantial new information to be
evaluated and considered in the 12month finding, we subsequently sought
and were granted a one month extension
with a new deadline of March 16, 2009.
This notice constitutes a 12-month
finding for the petition to list the
yellow-billed loon as threatened or
endangered. The petitioners provided
two listing options for consideration by
the Service: (1) Listing the yellow-billed
loon throughout its range, or (2) listing
the United States population of the
yellow-billed loon as a Distinct
Population Segment (DPS). Because we
find that listing the yellow-billed loon
rangewide is warranted at this time,
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there is no need to conduct further
analysis of whether listing the United
States population of the yellow-billed
loon as a DPS, which is a smaller
geographic entity than the entire range,
is warranted, as this consideration is
subsumed by the rangewide warranted
but precluded finding.
Outline of This Notice
In this notice, we first provide
background information on the biology
of the yellow-billed loon. Next, we
address each of the categories of factors
listed in section 4(a)(1) of the Act. For
each factor, we first determine whether
any stressors, or risk factors, appear to
be negatively affecting yellow-billed
loons anywhere within the species’
range. If we determine they are, then we
evaluate whether each of these risk
factors is resulting in population-level
effects that are significant to the
determination of the conservation status
of the species. If so, we describe it as a
‘‘threat.’’ The fact that we find a stressor
to be a threat to the species does not
necessarily mean that the species meets
the definition of threatened or
endangered. Rather, in the subsequent
finding section, we then consider each
of the stressors and identified threats,
individually and cumulatively, and
make a determination with respect to
whether the species is endangered or
threatened according to the statutory
standard.
The term ‘‘threatened species’’ means
any species (or subspecies or, for
vertebrates, distinct population
segments) that is likely to become an
endangered species within the
foreseeable future throughout all or a
significant portion of its range. The Act
does not define the term ‘‘foreseeable
future.’’ However, in a January 16, 2009,
memorandum addressed to the Acting
Director of the U.S. Fish and Wildlife
Service, the Office of the Solicitor,
Department of the Interior, concluded,
‘‘* * * as used in the ESA, Congress
intended the term ‘foreseeable future’ to
describe the extent to which the
Secretary can reasonably rely on
predictions about the future in making
determinations about the future
conservation status of the species.’’ In a
footnote, the memorandum states, ‘‘In
this memorandum, references to
‘reliable predictions’ are not meant to
refer to reliability in a statistical sense.
Rather, I use the words ‘‘rely’’ and
‘‘reliable’’ according to their common,
non-technical meanings in ordinary
usage. Thus, for the purposes of this
memorandum, a prediction is reliable if
it is reasonable to depend upon it in
making decisions’’ (M–37021, January
16, 2009).
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Species Biology
The yellow-billed loon is a migratory
bird. Solitary pairs breed on lakes in the
arctic tundra of the United States,
Russia, and Canada from June to
September. During the remainder of the
year the species winters in more
southern coastal waters of the Pacific
Ocean and the Norway and North Seas.
Non-breeding birds remain in marine
waters throughout the year, either in
wintering areas or offshore from
breeding grounds.
The following information regarding
the description and natural history of
the yellow-billed loon (American
Ornithologists’ Union 1998, p. 5) has
been condensed from the status
assessments conducted by North (1994)
and Earnst (2004), and updated with
information that has become available
since then.
Taxonomy and Description
The yellow-billed loon (Order
Gaviiformes, Family Gaviidae) is one of
the largest of the five loon species and
similar in appearance to the common
loon (Gavia immer). There are no
recognized subspecies or geographic
variations (American Ornithologists’
Union 1998, p. 5). A field characteristic
that distinguishes yellow-billed loons
from common loons is their larger
yellow or ivory-colored bill. Adults
weigh 4,000 to 6,000 grams (8.8 to 13.2
pounds) and are 774 to 920 millimeters
(30 to 37 inches) in length. Breeding
(alternate) plumage of adults of both
sexes is black on top with white spots
on the wings and underside, and white
stripes on the neck. Non-breeding
(basic) plumage is gray-brown with
fewer and less distinct white spots than
breeding plumage, with paler
undersides and head, and a blue-gray
bill. Hatchlings have dark brown and
gray down, and juveniles are gray with
a paler head (North 1994, p. 2). Yellowbilled loons are specialized for aquatic
foraging with a streamlined shape and
legs near the rear of the body, and are
unable to take flight from land.
Feeding Habits
Yellow-billed loons forage underwater
for fish and aquatic invertebrates.
Limited information exists on specific
prey species consumed. Marine prey
species collected from loons wintering
in southeast Alaska and Canada include
fish such as sculpins (Leptocottus
armatus, Myoxocephalus sp.), Pacific
tomcod (Microgadus proximus), and
rock cod (Sebastodes sp.), and
invertebrates such as amphipods
(Orchomonella sp., Anonyx nirgax),
isopods (Idothea sp.), shrimps
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(Pandalus danae, Spirontocaris
ochotensis), hermit crabs (Pagarus sp.),
and marine worms (Nereis sp.) (Bailey
1922, p. 205; Cottam and Knappen 1939,
p. 139; North 1994, pp. 6–7; Earnst
2004, pp. 9–10). Pacific sand dabs
(Citharichthys sordidus) were found in
a yellow-billed loon collected
extralimitally (i.e., outside the limits of
the species’ range) in Baja California
(Jehl 1970, p. 376) and sculpin
(Myoxocephalus scorpius) in a
specimen collected in Norway (Collett
1894, p. 280). Prey species taken in
other wintering grounds, such as in the
Yellow Sea (which supports 276 fish
species and 54 crustacean species;
UNDP 2002, p. 8) are unknown.
During the breeding season, foraging
habitats include lakes, rivers, and the
nearshore marine environment.
Successfully breeding adults feed their
young almost entirely from the broodrearing lake (North 1994, p. 14).
Ninespine sticklebacks (Pungitius
pungitius) and least cisco (Coregonus
sardinella) are thought to be the main
foods of chicks in Alaska (Earnst 2004,
p. 9). Other freshwater prey available in
Alaska that are likely utilized include
Alaska blackfish (Dallia pectoralis),
fourhorn sculpins (M. quadricornus),
amphipods, and isopods (Earnst 2004,
p. 9), as well as aquatic plant material
˚
¨
(Sjolander and Agren 1976, p. 460). In
arctic Russia, limited stomach content
analysis indicates sticklebacks, salmon,
crustaceans, beetles, and plant
vegetation are consumed during the
breeding season (Uspenskii 1969, p.
130).
Breeding Habitat and Territories
Yellow-billed loons nest exclusively
on margins of lakes in coastal and
inland low-lying tundra from 62° to 74°
North (N) latitude. Lakes that support
breeding loons have abundant fish
populations. Studies of yellow-billed
loon habitat have identified several
characteristics that predict loon
presence. These may be indirect
measures or correlates of the actual
characteristics necessary or preferred by
loons, such as fish availability.
Predictors of yellow-billed loon
presence on a lake include water depths
greater than 2 meters (m) or 6.5 feet (ft)
allowing for unfrozen water under the
ice during winter; large lake areas (at
least 13.4 hectares (ha) or 33 acres (ac));
connections to streams that may supply
fish; highly convoluted, vegetated, and
low-lying shorelines; clear water; and
dependable water levels (Earnst et al.
2006, pp. 230–233; Stehn et al. 2005,
pp. 9–10; North 1994, p. 6). Probability
of yellow-billed loon presence on a lake
increases with the absence of Pacific
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loons (Gavia pacifica) (Earnst et al.
2006, p. 233; Stehn et al. 2005, p. 9).
Breeding lakes may be near major rivers,
but are usually not connected to them,
possibly because greater fluctuations
associated with river connections may
flood nests or cause turbidity that
compromises foraging success (North &
Ryan 1989, p. 303). Falling water levels
may also expose loon nests to increased
risk of predation (Kertell 1996, p. 356).
Breeding territories (areas defended
against other yellow-billed loons and
other loon species, particularly Pacific
loons) may include one or more lakes or
parts of lakes. Territory size, likely
dependent upon lake size and quality,
ranged from 13.8 to greater than 100 ha
(34 to greater than 247 ac) on the
Colville River Delta, Alaska (North
1986, as cited in North 1994, p. 10). It
is thought that individual loons occupy
the same breeding territory throughout
their reproductive life. Some breeding
lakes are ‘‘known to be reoccupied over
long time spans’’ (North 1994, p. 10),
most likely by the same monogamous
pair (North 1994, p. 10), similar to
common loons (Evers 2004, p. 13).
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Nesting Sites and Behavior
Nest sites are usually located on
islands, hummocks, or peninsulas,
along low shorelines, within 1 m (3 ft)
of water. The nest location, which may
be used in multiple years, usually
provides a better view of the
surrounding land and water than other
available lakeshore locations. Nests are
constructed of mud or peat, and are
often lined with vegetation. One or two
large, smooth, mottled brown eggs are
laid in mid-to late June (North 1994, pp.
11–12). Egg replacement after nest
predation occurs rarely; unless failure
occurs very early in the season, the
short arctic summer probably precludes
the production or success of
replacement clutches (Earnst 2004, p. 8).
Hatching occurs after 27 to 28 days of
incubation by both sexes. Although the
age at which young are capable of flight
is unknown, it is probably similar to
common loons (8–9, possibly up to 11,
weeks). The young leave the nest soon
after hatching, and the family may move
between natal and brood-rearing lakes.
Both males and females participate in
feeding and caring for young (North
1994, p. 13).
Life History
There is no reliable scientific
information on lifespan and
survivorship, but as large-bodied birds
with low clutch size, yellow-billed
loons are probably K-selected (longlived and dependent upon high annual
adult survival to maintain populations).
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On average, individuals reach sexual
maturity at 3 years of age, but may not
acquire breeding territories until at least
4 years of age (North 1994, p. 15). The
average age at first breeding for common
loons is 6 years (Evers 2004, p. 18).
Territory occupancy and nesting
success of yellow-billed loons were
studied on the Colville River Delta
during 18 years between 1983 and 2007.
Ground-based surveys in 1983 and 1984
found 76 and 79 percent of the
territorial pairs nesting, respectively
(Field et al. 1993, p. 329). The same
territories studied in 1983 and 1984
were visited in 1989 and 1990, and 42
percent and 67–71 percent, respectively,
of the territorial pairs were found
nesting (Field et al. 1993, p. 329; North
1993, p. 46). Low nest occupancy
recorded in 1989 may have been a result
of surveys being conducted late in
incubation (July 9–16, 1989) after nests
of some pairs had already failed; weekly
monitoring surveys of nesting yellowbilled loons on the Colville River Delta
in 2005–2007 found that 19–36 percent
of the nests had failed by July 10–12 of
those years (Johnson et al. 2006, Table
5; Johnson et al. 2007, Table 5; Johnson
et al. 2008, Table 4). However, low nest
occupancy occurred in some years
during two long-term studies of yellowbilled loons on the Colville Delta. The
percentage of territorial pairs nesting
ranged from 39 percent to 89 percent
during a 6-year ground-based study
(1995–2000; Earnst 2004, p. 9) and from
43 percent to 76 percent (average of 58
percent) during 13-years of aerial
surveys (1993–2007; ABR, Inc. 2007,
Table 1; ABR, Inc., unpublished data).
Reproductive success, like nest
occupancy by territorial pairs, varied on
the Colville River Delta. Low
reproductive success has been attributed
to late ice melt or extreme flooding
(Earnst 2004, p. 9). Based on Mayfield
survival rates (a technique for
measuring nesting success in which the
number of days from discovery of the
nest to fledging or failure (exposure
days) is used to compute a daily nestsurvival rate) calculated for yellowbilled loons nesting on the Colville
River Delta in 1995–2000, 4 percent to
60 percent of eggs/chicks survived from
laying to age 6 weeks (Earnst 2004, p.
9). Apparent nesting success [(broods/
nests) × 100] based on broods counted
on aerial surveys conducted 8 weeks
apart during nesting and brood-rearing
ranged from 19 percent to 64 percent
annually in 13 years between 1993 and
2007 (ABR, Inc. 2007, Table 1; ABR,
Inc., unpublished data). During the last
three years (2005–2007) of this study,
weekly monitoring surveys were
conducted after nests were found.
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Apparent nesting success calculated
from these weekly surveys was 1–10
percent higher than calculations based
on nesting and brood-rearing surveys
conducted 8 weeks apart, because the
more frequent surveys identified nests
with chicks that did not survive to 5–
6 weeks of age (Johnson et al. 2006, p.
17; Johnson et al. 2007, p. 16; Johnson
et al. 2008, p. 15). The highest recorded
apparent nesting success on the Colville
River Delta was 71 percent in 2007
based on weekly monitoring surveys
(Johnson et al. 2008, p. 15).
Breeding Distribution
Yellow-billed loons nest near
freshwater lakes in arctic tundra of
Alaska on the Arctic Coastal Plain
(ACP), northwestern Alaska, and St.
Lawrence Island; in Canada east of the
Mackenzie Delta and west of Hudson
Bay; and in Russia on a relatively
narrow strip of coastal tundra from the
Chukotka Peninsula in the east and on
the western Taymyr Peninsula in the
west, with a break in distribution
between these two areas (Earnst 2004, p.
3; North 1993, p. 42; Red Data Book of
the Russian Federation 2001, p. 366;
Ryabitsev 2001, p. 22; Il’ichev and Flint
1982, p. 277; Pearce et al. 1998, p. 369).
Loons are sparsely distributed across
their range, although, perhaps because
of non-uniform quality of habitat, at a
large scale breeding birds are somewhat
clumped in distribution.
Breeding Bird Densities
Most of the breeding range of the
yellow-billed loon has not been
adequately surveyed, and only in Alaska
have surveys been conducted
specifically for breeding yellow-billed
loons. Unless otherwise noted, the
following discussion includes data from
waterfowl surveys for which loons were
not focal species. In these surveys,
density estimates were not corrected for
visibility bias and so are minimal
estimates (see discussion in Groves et al.
1996, pp. 193–194). Surveys enumerate
all yellow-billed loons seen on breeding
grounds, including an unknown
proportion of which are non-breeders
(Earnst et al. 2005, p. 300).
Alaska
Based on fixed-wing aerial survey
data (1992 to 2003 ACP and North Slope
Eider (NSE) surveys conducted by the
Service), Earnst et al. (2005, p. 300)
calculated that most of the population
on the ACP of Alaska occurred within
concentration areas with more than 0.11
individuals per square kilometer (km2).
Such areas comprised only 12 percent of
the surveyed area yet contained 53
percent of yellow-billed loon sightings.
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The largest concentration area was
between the Meade and Ikpikpuk
Rivers; it covered only 8 percent of the
survey area, but had 38 percent of
yellow-billed loon sightings (Earnst et
al. 2005, p. 300). Other notable
concentrations were on the Colville
River Delta and west, southwest, and
east of Teshekpuk Lake (Earnst et al.
2005, p. 300). In aerial lake-circling
surveys designed for yellow-billed loons
(fixed-wing aircraft were used 1992–
2000; helicopters were used 2001–
2007), the average density on the
Colville River Delta (363 km2 (140 mi2)
survey area) was 0.13 individuals per
km2 during 10 years from 1993 to 2004
(Johnson et al. 2005, p. 65), and 0.15 to
0.17 individuals per km2 from 2005 to
2007 (Johnson et al. 2006, p. 15; Johnson
et al. 2007, p. 16; Johnson et al. 2008,
p. 15). Similar surveys for yellow-billed
loons in a larger area (878 km2) (339
mi2) in the Northeast Planning Area
(NE) of the National Petroleum ReserveAlaska (NPR–A) in 2001–2004 indicated
densities there were lower (0.07
individuals/km2; Johnson et al. 2005, p.
68), except that the density in an area
adjacent to Fish and Judy Creeks was
similar to that of the Colville River Delta
(Johnson et al. 2005, p. 68; Johnson et
al. 2006, p. 15; Johnson et al. 2007, p.
16). In western Alaska, where fixedwing aerial surveys were also designed
specifically for loons, density on the
northern Seward Peninsula averaged
0.058 (standard error (SE)=0.011;
standard error is a measure of the
variability in the data) individuals/km2
over 2 years (Bollinger et al. 2008, p. 5).
Canada
In Canada, concentrations are found
on parts of Victoria and Banks Islands,
on the mainland, the Kent Peninsula,
east of Bathhurst Inlet and west of Ellice
River, the west side of Boothia
Peninsula, and the lake district between
Great Slave Lake and Baker Lake,
including the Thelon Game Sanctuary
(North 1993, p. 42). Densities obtained
in 2005 and 2007 from fixed-winged
aerial waterfowl surveys on southern
Victoria Island and the Kent Peninsula
ranged from 0.017 to 0.16 birds/km2
(Conant et al. 2006, pp. 2, 7; Groves in
litt. 2008); lower densities (0.004–0.027
birds/km2) were found in surveys on the
Queen Maud Gulf Migratory Bird
Sanctuary, King William Island,
Rasmussen Lowlands, and Kugluktuk
(Conant et al. 2007, pp. 10, 12; Groves
in litt. 2008). On western Victoria
Island, Raven and Dickson (2006, p. 24)
estimated densities from 0.004 to 0.08
birds/km2 from helicopter-based
waterfowl surveys. Hines (in litt. 2008)
estimated 0.01 yellow-billed loons/km2
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on Banks Island from helicopter-based
waterfowl surveys in 1992 and 1993.
Russia
In Russia, breeding concentrations
have been identified on the Chukotka
(Chukotskiy) Peninsula (Il’ichev and
Flint 1982, p. 280; Solovyov 1992, p.
21), Kyttyk Peninsula and Ayon Island
in western Chukotka (Solovyova 2007,
p. 6), and the western Taymyr Peninsula
(Krechmar 1966, p. 200; Il’ichev and
Flint 1982, p. 277). Hodges and Eldridge
(2001, pp. 141–142), using fixed-winged
aircraft in the only aerial waterfowl
survey of the eastern Siberian coast,
found concentrations of approximately
0.01 birds/km2 on the Cape Schmidt
coast of the Chukotka Peninsula,
between the Indigirka and Yana River
Deltas, and between the Indigirka and
Kolyma Deltas. Post-breeding density on
Kyttyk Peninsula in western Chukotka
was approximately 0.52 birds/km2
(including young birds) during late
July–August 2003–2007 (calculated
from ground surveys, Solovyova 2007,
p. 6). No density estimates are available
for the Taymyr Peninsula.
Nest Densities
Nest density on 363 km2 (140 mi2) of
the Colville River Delta, Alaska, ranged
from 0.03 to 0.08 nests/km2 during 13
years of aerial surveys for yellow-billed
loons during 1993–2007 (Johnson et al.
1999, p. 44; Burgess et al. 2003, p. 36;
Johnson et al. 2003, p. 43; Johnson et al.
2004, p. 74; Johnson et al. 2005, p. 64;
Johnson et al. 2006, p. 15; Johnson et al.
2007, p. 16; Johnson et al. 2008, p. 15).
Nest density in an 878 km2 (339 mi2)
survey area of NE NPR–A was 0.03
nests/km2 in each year during 2002–
2004. Higher densities within this area
were found along Fish and Judy Creeks
(helicopter-based surveys; Johnson et al.
2005, p. 68). In Russia, Solovyov (1992)
reported 0.18 nests/km2 on a 27.6 km2
(10.6 mi2) plot searched from the ground
on Belyaka Spit near Kolyuchin Bay on
the Chukotka Peninsula. On the Kyttyk
Peninsula in western Chukotka, yellowbilled loons nest on approximately 25
percent of lakes larger than 4 ha (9.9
acres) (Solovyova 2007, p. 6).
Foraging Distribution During Breeding
Season
Yellow-billed loons use nearshore and
offshore marine waters adjacent to their
breeding areas for foraging in summer.
Such habitats are likely used by both
breeding adults and younger or nonterritorial birds (Earnst 2004, p. 7).
Earnst (2004, pp. 6–7) reviewed yellowbilled loon distribution information
from fixed-wing aerial waterfowl
surveys that Fischer et al. (2002)
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conducted in 1999 and 2000 off the
coasts of Canada’s arctic islands and the
ACP of Alaska between Cape Halkett
and Brownlow Point. Similar surveys
conducted between Barrow and
Demarcation Point in 2001 also
included yellow-billed loon
observations in Elson Lagoon (Fischer
2001, p. 4; Fischer and Larned 2004, p.
146). During fixed-wing aerial surveys
for common eiders in late June of 1999
through 2007, between 23 and 99
yellow-billed loons were observed in
nearshore waters and along barrier
islands of the Beaufort and Chukchi
Seas (Dau and Larned 2007, p. 18).
Yellow-billed loons used lagoons and
nearshore waters along the coast of St.
Lawrence Island in summer in the 1950s
(Fay and Cade 1959, pp. 92, 100). In
Russia, Solovyova (coastal boat surveys;
2007, p. 6) reported densities of 0.24
birds/km2 using coastal waters near the
Kyttyk Peninsula and Ayon Island at the
northern end of Chaun Bay in western
Chukotka, and 0.04 birds/km2 at the
southern end of Chaun Bay near the
Chaun River Delta in 2006. Vronskiy
(1987, p. 30) observed individual
yellow-billed loons and pairs in bays
100–150 m (328–492 ft) offshore of
northwestern Taymyr during summer.
Yellow-billed loons occurred in summer
along the coast of Wrangel Island,
although there were no indications of
nesting on the island (Stishov et al.
1991, p. 20). In boat-based surveys in
the Kara and Barents Seas, arctic (Gavia
arctica) and red-throated (G. stellata)
loons were abundant in the nearshore
marine waters of the western Kara Sea
and in the Ob’ and Yenisey estuaries,
especially in Baidaratskaya Bay, and
occurred in smaller numbers in the
Pechora Bay in the Barents Sea in
August and September 1995, but no
yellow-billed loons were observed
(Decker et al. 1998, pp. 9, 11). In
subsequent boat surveys between 1998
and 2003, only one yellow-billed loon
was observed in mid-August 1998 in
coastal waters northeast of Dolgy Island
(west of Vaigach Island) in the Pechora
Sea (M. Gavrilo, in litt. 2008).
Wintering Habitat and Distribution
Wintering habitats include sheltered
marine waters less than 30 m (98.4 ft)
deep, such as fiords and areas between
islands on the inner coast in Norway
(Strann and ;stnes 2007, p. 2). Schmutz
(2008, p. 1) found that throughout
migrating and wintering seasons,
yellow-billed loons marked with
satellite transmitters occurred from 1 to
20 miles offshore. The wintering range
includes coastal waters of southern
Alaska and British Columbia from the
Aleutian Islands to Puget Sound; the
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Pacific coast of Asia from the Sea of
Okhotsk south to the Yellow Sea; the
Barents Sea and the coast of the Kola
Peninsula; coastal waters of Norway;
and possibly Great Britain (Earnst 2004,
pp. 13–14; North 1993, pp. 42–43;
Ryabitsev 2001, p. 22; Schmutz in litt.
2008, p. 1; Strann and ;stnes 2007, p.
2; Burn and Mather 1974, p. 278; Gibson
and Byrd 2007, p. 68). A small
proportion of yellow-billed loons may
winter in interior lakes or reservoirs in
North America (North 1994, p. 3).
Winter population distribution and
numbers of yellow-billed loons are not
well documented, but some information
is available from marine bird surveys.
Earnst (2004, p. 14) summarized loon
observations in boat-based marine bird
population surveys in Lower Cook Inlet,
Prince William Sound, and Kodiak
Island. In these surveys, estimates of
yellow-billed loons were in tens to low
hundreds, with wide confidence limits.
In many cases, loons were not identified
to species. Strann and ;stnes (2007, p.
3) counted 1,160–1,605 yellow-billed
loons on surveys conducted off the coast
of Norway from 1986 to 1994,
confirming Norway as the most
important known wintering area for the
species in Europe. No surveys have been
conducted in Asian wintering areas. In
some regularly used wintering areas
such as the Yellow Sea, the Aleutian
Islands, and Great Britain, the yellowbilled loon’s small population and
scattered marine distribution may have
contributed to the impression that
yellow-billed loons are vagrants or rare
visitors (Lepage 2008, p. 1; Gibson and
Byrd 2007, p. 68; Dudley et al. 2006, p.
533; Scott and Shaw 2008, pp. 241–
248).
Immature loons and possibly some
non-breeding adults stay in wintering
areas throughout the year (North 1994,
p. 4). Earnst (2004, pp. 11–12)
summarized yellow-billed loon
observations in summer marine boatbased surveys conducted in lower Cook
Inlet and Prince William Sound in
southcentral Alaska, and in southeast
Alaska. Estimates from all these surveys
totaled only 339 yellow-billed loons, but
many loons were not identified to
species (Earnst 2004, p. 11). In boatbased surveys of murrelets conducted in
July of 2002–2004 from Icy Bay to
LeConte Bay in southeast Alaska,
Kissling et al. (2007, Appendices 7, 8)
counted 20 yellow-billed loons. Yellowbilled loons have been observed
throughout summer months in the
Aleutians (Gibson and Byrd 2007, p.
68). According to the Red Data Book of
Kamchatka (2006, p. 92), non-breeding
birds occur off the coast of Kamchatka
in summer.
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Migration
Yellow-billed loon migration routes
are thought to be primarily marine.
Schmutz (in litt. 2008, p. 1) found that
yellow-billed loons marked with
satellite transmitters generally remained
between 1 and 20 miles from land
during migration and winter. Yellowbilled loons migrate singly or in pairs,
but gather in polynyas (areas of open
water at predictable, recurrent locations
in sea-ice covered regions), ice leads
(more ephemeral breaks in sea ice, often
along coastlines), and early-melting
areas off river deltas near breeding
grounds in spring along the Beaufort Sea
coast of Alaska and Canada (Barry et al.
1981, pp. 29–30; Barry and Barry 1982,
p. 25; Woodby and Divoky 1982, p. 406;
Johnson and Herter, 1989, p. 9; Barr
1997, pp. 12–13; Alexander et al. 1997,
pp. 15, 17; Mallory and Fontaine 2004,
pp. 52–53).
These observations of yellow-billed
loons in the Beaufort Sea during
migration establish that at least some
yellow-billed loons breeding in
Canada’s Arctic Islands and along the
adjacent Canadian coast use this
migration route. North (1993, pp. 45–46)
examined evidence of alternative
migration routes for yellow-billed loons
wintering in southeast Alaska and
British Columbia, suggesting that they
could migrate overland to mainland
breeding areas in Canada, particularly
around Great Slave Lake. Yellow-billed
loons have been observed on inland
lakes in Canada and Alaska (North 1993,
pp. 43, 46). The existence of this route
is still hypothetical, and the number of
yellow-billed loons in interior mainland
Canada is highly uncertain (discussed
below under Population Size).
Yellow-billed loons breeding in
Alaska have been studied to determine
migration routes. Nineteen yellow-billed
loons captured on the ACP between
2002 and 2008 were outfitted with
satellite transmitters (Schmutz in litt.
2008, p. 1). All of them migrated to
Asia, predominantly south along the
Russian coastline from the Chukotka
Peninsula (either through the Bering
Strait or across the mountains from the
north side of the Chukotka Peninsula to
the Gulf of Anadyr), and along the
Kamchatka coast. They wintered in the
Yellow Sea and Sea of Japan off China,
North Korea, Russia, and Japan (near
Hokkaido). All 10 yellow-billed loons
fitted with transmitters on the Seward
Peninsula, Alaska, in 2007 and 2008
also used the Bering Strait region after
leaving breeding grounds. Five of these
migrated to Asian grounds as described
above for ACP breeding birds; the other
5 wintered throughout the Aleutian
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Islands from Shemya Island in the west
to the Semidi Islands off the coast of the
Alaska Peninsula (Schmutz in litt. 2008,
p. 1). Most of these yellow-billed loons
departed breeding areas in late
September, arrived in wintering
locations in mid-November, started
spring migration in April, and arrived
on breeding grounds in the first half of
June; these dates are consistent with
breeding ground arrival dates reported
by North (1994, p. 5). Non-breeders or
failed nesters may start fall migration in
July.
The migration routes of yellow-billed
loons breeding in Russia have not been
studied. Because of the proximity of the
Chukotka Peninsula to the ACP in
Alaska, and the fact that ACP breeding
yellow-billed loons use the Chukotka
Peninsula during migration (Schmutz in
litt. 2008, p. 1), it is likely that some or
all yellow-billed loons from eastern
Russia migrate through the Bering Strait
to Asian wintering areas.
Population Size
ACP, Alaska
Yellow-billed loon population indices
on the ACP of Alaska were determined
by two independent fixed-wing aerial
transect surveys conducted each year by
the Service’s Migratory Bird
Management program. Surveys were
flown in early June each year from 1992
through 2008 (NSE survey, 1992–2008,
an average of 1,304 km2 (503.5 mi2)
transect area that sampled a total area of
30,465 km2 (11,763 mi2), for 4.3 percent
coverage) and late June each year from
1986 through 2006 (ACP survey, 1986–
2006, average of 1,256 km2 (485 mi2)
transect area which sampled a total area
61,645 km2 (23,801 mi2), for 2.0 percent
coverage of a larger area than that
covered by the NSE survey). The
average population index from the NSE
survey is 1,119 yellow-billed loons (95
percent confidence interval (CI) = 1,012
to 1,226, Larned et al. 2009, p. 24).
(Note: In order to estimate the reliability
of a sample statistic, such as an average,
it is common to set confidence limits to
it (Sokal and Rohlf 1995, p. 139). The
limits will show the maximum and
minimum numbers the statistic (e.g.,
average) is likely to be, along with a
measure of that likelihood (e.g., 95
percent). So, when an average number
of birds, for example, is reported,
followed by a confidence interval, the
confidence interval shows the statistical
range of values that provides cutoff
points for the likely values for the
average.) The long-term mean from the
ACP survey is 2,611 loons (95 percent
CI = 2,218 to 3,005; Mallek et al. 2007,
p. 10; USFWS unpublished data). The
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confidence intervals around these 16and 21-year means incorporate the
variation due to within-year sampling
error, the spatial variability among
transects and within strata, and
variation among years related either to
detection rate (observer ability, habitat
change, weather conditions) or the
availability of birds to be seen (arrival
or departure of population components,
behavior associated with nesting
chronology). One study integrated
results from both the early and late
surveys, incorporating covariates
adjusting for detection rates (Earnst et
al. 2005). The 12-year mean (1992
through 2003) resulted in an estimate of
2,221 individuals (95 percent CI =
1,209–3,233) in early June and 3,369
individuals (95 percent CI = 1,910–
4,828) in late June (Earnst et al. 2005, p.
295). Another estimate of population
size was determined by lake-circling
aerial searches of greater than 7-ha
(17.3-acre) lakes on 7 × 7-km (4.35 ×
4.35-mi) plots as part of a 2003–2004
study of yellow-billed loon habitat
preferences (Stehn et al. 2005, pp. 1–
37). This survey was flown from June 15
through 22 each year. Based on average
density observed, the estimated total
population index was 2,544 (95 percent
CI = 1,780–3,308) yellow-billed loons
(Stehn in litt. 2008, p. 1).
Western Alaska
Seward Peninsula and Cape
Krusenstern fixed-wing aerial lakecircling surveys, on 12 × 12-km (7.46 ×
7.46-mi) sample plots, were flown in
June of 2005 and 2007, and resulted in
an estimate of 431 (95 percent CI = 280–
582) yellow-billed loons on these
western Alaska breeding grounds
(Bollinger et al. 2008, p. 1). Additional
aerial transects sampling an area of
15,234 km2 (5,882 mi2) were flown on
Selawik National Wildlife Refuge and
adjacent wetlands in June in the years
1996 and 1997 (Platte 1999, p. 3), but
only three yellow-billed loons were
sighted, resulting in an estimated mean
population index of 44 birds (95 percent
CI = 0–95) (USFWS unpublished data).
Yellow-billed loons were documented
nesting on St. Lawrence Island in the
1950s (Fay and Cade 1959, pp. 84, 100),
but there is no more recent information.
Adding western Alaska population
figures to those from the ACP results in
an estimated total of 3,000 to 4,000
yellow-billed loons on breeding grounds
in Alaska.
Canada
Although overall breeding population
estimates for yellow-billed loons in
Canada do not exist (https://www.bsceoc.org/clls-bw1.html, accessed May 19,
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2008), and yellow-billed loons are not
summarized in the Waterfowl
Population Status annual reports
compiled by the U.S. and Canadian
governments for North American
Waterfowl (USFWS 2007, pp. 1–62),
several recent fixed-wing aerial
waterfowl surveys included loon
observations in parts of Nunavut and
Northwest Territories. Loons were not
the focus of the surveys, so it is possible
that observer effort or identification
ability varied, and no visibility
correction factors or seasonal timing
factors were applied. Helicopter surveys
yielded estimates ranging from 659 (SE
359) to 1,784 (SE 502) on northwest
Victoria Island, and from 98 (SE 70) to
258 (SE 146) birds in the southwest part
of the island (Raven and Dickson 2006).
A fixed-winged survey included Kent
Peninsula and southeastern Victoria
Island in 2005, and Queen Maud Gulf,
King William Island, Rasmussen
Lowlands, and near Kugluktuk in 2006;
all areas from both years were repeated
in 2007 but with fewer transects
sampled per unit area. The combined
estimate for both areas from 2005–2006
fixed-winged surveys and the 2007
estimate were similar, at 2,500–3,000
birds (Conant et al. 2006, p. 7; Conant
et al. 2007, p. 12; Groves in litt. 2008).
Hines (in litt. 2008) estimated there
were 500–1,000 yellow-billed loons on
Banks Island, based on helicopter aerial
surveys conducted in 1992 and 1993.
The range of these point estimates
suggests that between 3,750–6,000 birds
occur on breeding grounds in the
surveyed areas.
The rest of the yellow-billed loon’s
range on the Canadian mainland has not
been surveyed. Based on the vast
number of large, fish-bearing lakes north
of treeline (an area of 500,000–750,000
km2) (193,051–289,577 mi2) minus the
surveyed areas on the mainland (46,000
km2), (17,761 mi2) and using
opportunistic observations of yellowbilled loons by Northwest Territory and
Nunavut checklist survey cooperators
over the last decade, Poter (in litt. 2008,
p. 2, adjusted from Hines in litt. 2008,
p. 1) calculated that a density of 0.01–
0.02 birds/km2 would yield an estimate
of 4,500–14,000 birds in mainland
breeding areas in Canada, not including
surveyed areas in the arctic described in
the previous paragraph. This estimate is
based on a very large land area bounded
at the southern end by an area of
documented yellow-billed loon
breeding between Great Slave Lake and
Baker Lake, particularly in or near the
Thelon Game Sanctuary (North 1993, p.
42). Between this area and the arctic
coast is a large area where breeding has
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not been documented (North 1993,
Figure 2). Fair (2002, p. 30) estimated
the yellow-billed loon population on
interior Canadian breeding grounds to
be 4,800, using a density of 0.02 loons
in a 100,000 km2 area around the
Sanctuary, and a lower density of 0.007
for the wider area of 400,000 km2. Fair’s
estimate of 4,800 is close to the lower
end of Poter’s (2008, p. 1) estimate of
4,500. We believe Fair’s analysis more
accurately reflects likely yellow-billed
loon distribution in Canada, because it
reflects a lower average density for the
large area where breeding has not been
documented. Combining the 4,500 to
14,000 breeding birds estimated for
interior Canada, and 3,750 to 6,000
breeding birds estimated for the arctic
(and rounding to thousands), we
conclude that the Canadian breeding
population size is 8,000 to 20,000, but
that it is most likely at the lower end of
this range.
Russia
Information on the breeding-ground
population size of yellow-billed loons
for Russia is limited. Hodges and
Eldridge (2001, Appendix 2) estimated
674 yellow-billed loons (coefficient of
variation (C.V., a measure of dispersion
in a probability distribution) 0.55) in a
157,611-km2 (60,854–mi2) fixed-wing
aerial survey area of the eastern Siberia
arctic coast from Kolyuchin Bay to the
Lena River Delta. We know of no other
loon surveys within the breeding range
of the yellow-billed loon in Russia. Red
Data Books for the Russian Federation
(2001, pp. 366–367), Yakutia (1987, p.
33), and the Northern Far East of Russia
(1998, pp. 97–98) do not offer
population estimates. Kondratiev (1989,
p. 37) estimated that 2,000 birds nested
in Chukotka, but did not give a basis or
sources for his estimate. Fair (2002, p.
31) projected, based on this estimate of
2,000 birds in Chukotka (Kondratiev
1989, p. 37), that another 2,000 nested
on the Taymyr Peninsula, and that
perhaps another 1,000 were scattered
across the arctic coast, giving 5,000
birds on Russian breeding areas.
Syroechkovsky (in litt. 2008) suggested
(based on field observations but not
scientific surveys) that the number of
birds on breeding grounds (including
non-breeding birds) is around 3,000 for
Chukotka, 500 for Yakutia, and about
1,200 for Taymyr, for a total of around
4,700 birds. However, Solovyova (in.
litt. 2008, p. 1; calculated from
Solovyova 2007, p. 6) recently estimated
the post-breeding population of the
Kyttyk Peninsula on Chaun Bay in
western Chukotka at 1,000, and the
post-breeding population of nearby
Ayon Island at 900 birds. Given
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Solovyova’s (in. litt. 2008, p. 1)
estimates for her study area in
Chukotka, she estimated that the total
breeding ground population in
Chukotka might be as high as 5,000
birds. If the Chukotka population is
5,000, the total for Russia could be as
high as 8,000 based on habitat
availability. Thus, our best information
suggests the Russian breeding
population is between 5,000 and 8,000
birds.
In summary, the global breeding
ground population size for yellow-billed
loons is unknown, but probably at the
lower end of the range of 16,000 to
32,000. The Alaska population estimate
of 3,000 to 4,000 is derived from
surveys. Less certain estimates based on
the amount of available habitat (plus
limited survey data) are the lower end
of the range of 8,000 to 20,000 birds in
Canada, and 5,000 to 8,000 in Russia.
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Population Trend
Alaska
The only population trends available
for yellow-billed loons breeding in
Alaska are on the ACP, where the ACP
and NSE waterfowl surveys are
conducted. We note that because we
count only the breeding component of
the population, the total population
could decline without being detected for
a number of years. This could occur
because increased mortality of breeding
birds could be masked by movements of
birds without territories (either subadult birds or adults which have not
found territories) into vacated
territories. With this caution, we believe
the time series of at least 17 years for the
surveys described below gives us a
reasonably reliable data set for
observing population trends, and these
data represent the best information
available at this time.
A population growth rate, or lambda,
less than 1.00 would indicate
population decline (negative ‘‘growth’’),
while a lambda greater than 1.00 would
indicate population growth. For the
ACP survey 1986–2006, the average
growth rate was 0.9886 (95 percent CI =
0.9625–1.0154) (Mallek et al. 2007, p.
21), and for the NSE survey 1992–2008
(a smaller area than that covered by the
ACP survey, and surveyed earlier in
June), the average growth rate was 1.016
(95 percent CI = 0.995–1.036)
(calculated from Larned et al. 2009,
Figure 1). Thus, these surveys provide
slightly conflicting perspectives, with
one suggesting a stable or slightly
declining population (with a point
estimate of a decline of 1.1 percent/yr.)
and the other suggesting a stable or
slight increasing population (with a
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point estimate of an increase of 1.6
percent/yr.) on the ACP.
Earnst et al. (2005, pp. 289–304)
sought to improve the estimates above
by using a statistical model that takes
into account possible confounding
factors of survey type, spring timing,
and observer experience. They used this
model to analyze ACP and NSE survey
data through 2003. Controlling for these
confounding factors, they (p. 298)
estimated average population growth
rate to be 0.991 (95 percent CI = 0.964–
1.018), also indicating a stable or
slightly declining population.
We also examined a subset of the NSE
data through 2008 that included only
the observations of the most consistent
and experienced pilot-observer, who has
flown all 16 early-June NSE surveys
during 1992–2008. Each survey includes
observations of two observers: the pilotobserver in the left-side seat of the
aircraft, and a second observer in the
right-side seat. There have been
numerous ‘‘right-side observers’’ over
the course of the NSE survey. Each of
these observers has a different ability to
see and identify birds, and this ability
often increases over successive surveys
as the observer gains experience. Our
analysis of the left-side pilot-observer
eliminated the necessity to estimate the
variable magnitudes of influence of
right-side observer experience. In
addition, the increased interest in
yellow-billed loons in 2002 may have
influenced new right-side observers to
search more intensively for yellowbilled loons than earlier observers, who
focused on waterfowl. Our analysis of
the pilot-observer data from the NSE
survey also eliminated the need to
reconcile the later timing and different
survey extent of the ACP survey. The
average growth rate using this subset of
data was slightly lower and more
precisely estimated at 0.986 (95 percent
CI = 0.967–1.006) (USFWS unpublished
data) than the estimate of 0.991 from
Earnst et al.’s (2005, p. 298) model, and
the results also indicate a relatively
stable or slightly declining population.
In summary, the information available
from the ACP does not allow us to
precisely determine current population
trends. Two surveys and multiple
analytical approaches used to control
for confounding factors provide
estimates indicating trends ranging from
slightly increasing to slightly
decreasing, and all estimates have 95
percent CIs that include a lambda of 1.0,
indicating that possible trends cannot be
distinguished from population stability
with reasonable certainty. Although the
population trend on the ACP is
uncertain, we conclude that the number
of breeding yellow-billed loons on the
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ACP breeding grounds is either stable or
declining slightly, with point estimates
from models controlling for
confounding factors estimating decline
on the order of ∼1 percent per year. We
will continue to look for ways to
improve our ability to detect trends.
Surveys in western Alaska have not
been conducted for a long enough
period (2005 and 2007) to detect trends.
Russia
In Russia, recent data are fragmentary,
making it difficult to determine trends.
In the west, the Red Data Book of the
Russian Federation (2001, p. 366) stated
that the species no longer nests in
European Russia where it was formerly
found, such as the Kola Peninsula, the
archipelago of Novaya Zemlya, and
Vaigach and Ainovy Islands in the Kara
Sea, although it is unclear how
abundant or widespread the species was
in these areas historically. (However,
Kalyakin (2001, p. 10) reports finding it
nesting on Novaya Zemlya, although it
is ‘‘extremely rare.’’) Similarly,
according to the Red Data Book of the
Yamal-Nenets Autonomous District
(1997) near the western end of the
Russian breeding range, in the previous
20 years only a few non-breeding
yellow-billed loons were recorded in the
District. Strann (in litt. 2008) speculated
that since the early 1990s there may
have been a decline in the number of
yellow-billed loons in the main Norway
wintering area, which would be
consistent with a western Russian
breeding ground range contraction if
birds nesting in western Russia migrate
to Norway for winter (which seems
logical). We were unable to find either
the source of the Red Data Book
statements or supporting evidence for
this potential range contraction. In
eastern Russia, yellow-billed loons
apparently no longer nest along the
northern coast of the Sea of Okhotsk
where they occurred 30–50 years ago,
nor on the Anadyr River delta (Red Data
Book of the Russian Federation 2001, p.
366; Red Data Book of the Northern Far
East of Russia 1998, p. 97). However,
Solovyova (in litt. 2008) reported that
the number of breeding yellow-billed
loons may be increasing in some
locations in eastern Siberia, specifically
near Chaun Bay in western Chukotka,
and at Belyaka Spit near Kolyuchin Bay
in northeastern Chukotka.
In summary, we found
unsubstantiated reports that the species
may no longer be found in parts of its
historical range in Russia, but there is
somewhat contradictory information for
some areas and a lack of survey data for
all areas. Yellow-billed loons may also
be increasing in some areas in Russia.
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We conclude that we do not have
reliable trend information for the
Russian breeding grounds.
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Canada
As described above for Population
Size, survey data for Canadian breeding
grounds cover a small portion of the
range, and have not been conducted for
enough years to analyze trends. We
conclude that we do not have reliable
trend information for Canadian breeding
grounds.
To summarize rangewide population
trend information, we have reliable data
indicating that the ACP breeding
population is stable or slightly
declining. We do not have reliable
evidence from other breeding areas that
breeding populations are increasing or
decreasing. There have been no surveys
of yellow-billed loons on wintering
areas, so we have no trend information
from those areas.
Population Resiliency
Certain intrinsic aspects of yellowbilled loon ecology and demography,
including low and variable productivity,
adult survival, and low population
numbers, are relevant to the species’
status. Stable populations of K-selected
species, such as the yellow-billed loon,
are characterized by low annual
productivity rates balanced with high
annual survival rates, meaning that
individuals must live many years to
replace themselves with offspring that
survive to recruit into the breeding
population. Low productivity means
that depleted K-selected species have
lower recovery potential and slower
recovery rates following population
declines than r-selected species, which
are characterized by high annual
productivity. Factors that reduce
productivity, including loss of
productive breeding habitats, reduction
in prey populations, and increases in
nest predators, may further constrain Kselected species’ recovery potential.
Further, most arctic species are
characterized by variable annual
productivity, given the vagaries and
severity of arctic weather, fluctuations
in predator-prey relationships, and
other aspects of arctic ecology. The
population impact of threats that reduce
productivity could be magnified if
coincident with an infrequent year of
otherwise high productivity.
Although factors that compromise
productivity can cause populations to
decline, adult survival is likely the more
important determinant of K-selected
species’ population size and persistence
(Smith and Smith 2001, p. 235). If
enough adults are removed from the
population prior to replacing
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themselves (i.e., adult survival is
decreased), the population will decline.
Perhaps most pertinent to a discussion
of extinction, rare species—those with
low numbers—are intrinsically closer to
a threshold below which recovery is not
possible (i.e., minimum viable
population) (Hunter 1996, p. 137).
These intrinsic aspects of yellowbilled loon ecology and demography
signal the continuing need to monitor
yellow-billed loon populations, despite
the fact that the species continues to be
widely distributed across both its arctic
breeding range, which is nearly
holarctic, and in its wintering range.
Factors Affecting the Yellow-Billed
Loon
Section 4(a)(1) of the Act (16 U.S.C.
1533(a)(1)) and regulations promulgated
to implement the listing provisions of
the Act (50 CFR part 424) set forth the
procedures for adding species to the
Federal Lists of Endangered and
Threatened Wildlife and Plants. A
species may be determined to be an
endangered or threatened species due to
one or more of the five factors described
in section 4(a)(1) of the Act. Below, we
provide a summary of our analysis of
threats to the yellow-billed loon.
Factor A: Present or Threatened
Destruction, Modification, or
Curtailment of the Habitat or Range
We considered whether yellow-billed
loon habitats are threatened by oil and
gas development (including
disturbance, changes in freshwater
chemistry and pollutant loads, and
changes in freshwater hydrology), by
degradation of the marine environment
from pollution or overfishing, or by
climate change. Potential threats from
oil and gas development are addressed
by the petitioners under Factor E, but
are discussed here under Factor A
because they are potential mechanisms
for rendering breeding habitats
unsuitable. Potential direct impacts on
loon mortality associated with
development, such as increased
predation and oil spills, are discussed
under Factors C and E, respectively.
Terrestrial Oil and Gas Development
Terrestrial and marine oil and gas
development occurs in the range of the
yellow-billed loon. Here we discuss
terrestrial development in Alaskan and
Russian breeding grounds. We are not
aware of any terrestrial oil or gas
development within the breeding range
of the yellow-billed loon in Canada;
planned terrestrial development on the
Mackenzie River Delta is outside the
breeding range, although activity there
could affect loons migrating through
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adjacent marine waters. Marine
activities related to oil and gas
development are discussed under Factor
E.
Much of the yellow-billed loon’s
breeding habitat in Alaska is within
areas available for oil and gas leasing
and development. Approximately threequarters of the yellow-billed loons that
nest in Alaska, and over 90 percent of
those that nest on Alaska’s ACP, occur
within the 9.5-million-ha (23.5-millionac) NPR–A (Earnst et al. 2005, p. 300),
in areas that are leased or available for
leasing for oil and gas exploration and
development. Approximately 29 percent
of yellow-billed loons breeding on the
ACP nest in NPR–A tracts that have
been leased (Stehn and Platte, U.S. Fish
and Wildlife Service, in litt. 2008, p. 1),
and 25 exploration wells were drilled
during the period 2000–2007 (https://
www.blm.gov/ak/st/en/prog/energy/
oil_gas/npra.html, accessed 3 June
2008). The Northwest Planning Area
(NW) NPR–A Integrated Activity Plan/
Environmental Impact Statement Record
of Decision (ROD) (USDOI–BLM 2004a,
p. 5) has made 100 percent of the NW
NPR–A available for leasing. The Final
NE NPR–A Supplemental Integrated
Activity Plan/Environmental Impact
Statement ROD (USDOI–BLM 2008b, p.
1) allows leasing of 86 percent (1.6
million ha, or 3.94 million ac) of the NE
NPR–A immediately, and an additional
9 percent beginning in 2018. Virtually
all yellow-billed loon breeding habitat
in the NE NPR–A is within areas
currently available for leasing (USDOI–
BLM 2008a, Volume 6, Maps 2–4 and 3–
10).
If offshore development occurs in the
Chukchi Sea, it is anticipated that a 500km (300-mi) oil pipeline will be built
across the NPR–A from the coast
between Icy Cape and Point Belcher to
the Trans-Alaska Pipeline (USMMS
2008, p. IV–10). The State of Alaska also
leases rights to oil and gas development
on its land, including the Colville River
Delta (ADNR 2008, p. 1), where
development has already occurred
within the range and habitats of the
yellow-billed loon (ADNR 2008, p.1).
Thus, as a result of past and possible
future oil and gas lease sales, and
ongoing exploratory efforts, a significant
portion of the yellow-billed loon’s
breeding habitat in NPR–A is subject to
potential oil and gas development.
Additionally, resource development in
adjacent offshore areas may result in the
construction of pipelines across
breeding habitat in NPR–A.
Although lease sales and exploratory
efforts set the stage for possible future
development in yellow-billed loon
breeding habitat in northern Alaska,
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determining the likelihood and timing
of eventual development is difficult. In
northeast NPR–A, several satellite
production pads associated with
existing infrastructure and facilities
outside NPR–A at the Alpine field on
the Colville River delta are in various
stages of planning, permitting, and
construction. It is very likely that within
the next 10 to 20 years at least 5 to 7
satellite production pads feeding the
existing central processing facility will
be in operation, with some pads on
State lands on the delta and some on
adjacent Federal lands in NPR–A.
Elsewhere in NPR–A the likelihood and
timing of possible future development
are more difficult to predict. BLM
estimates that exploratory activities take
roughly 10 years before construction
begins (USDOI–BLM 2008c, p. 13), with
roughly 70 years from the initiation of
exploration until final field
abandonment. Initial exploratory
activities have commenced in some
areas in NPR–A; exploration has yet to
begin on some existing leased tracts
elsewhere; and other lands have not yet
been leased or offered for lease. Thus,
yellow-billed loon habitat in the
Colville River delta and adjacent NPR–
A varies in its potential for future oil
and gas development, and the timing of
development, where it occurs, will be
staggered starting with imminent
development on and near the Colville
River delta, followed by exploration,
construction, and production over a
period of several decades elsewhere,
persisting for at least 70 years and
possibly longer in various areas.
Terrestrial oil development is
ongoing, and likely to increase, at the
western edge of Russian yellow-billed
loon breeding range. These areas have
never been systematically surveyed for
loons, so the historical occurrence and
degree to which development areas
overlaps areas used by loons is
unknown. On the Yamal Peninsula, the
largest gas field is the Bovanenkovskeo
field, which is projected, beginning in
2011, to produce approximately 115
billion cubic meters (4 trillion cubic ft)
of gas, which will be transported by new
railways and a 2,451-km (1,523-mi) long
pipeline currently under construction
(Barents Observer 2008, p. 1). A
liquefied-natural-gas plant is planned
on the Kara Sea coast of the peninsula.
The Yuzhnoe-Khykchuyu oil field in the
Timan-Pechora province near the port of
Varandey on the Pechora Sea is among
the largest in Russia, and is planned as
an anchor field for further development
(ConocoPhillips 2008, p. 1). Major
western Siberian oil fields in the
Pechora River basin of the Komi
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Republic have operated for decades
upstream of yellow-billed loon breeding
range, and a large mining industry
operates out of Norilsk on the Taymyr
Peninsula. Gazprom, Russia’s largest oil
and gas company, is developing new
discoveries in Chukotka near Anadyr
(Gazprom Neft 2004, p. 1). In addition
to these activities at the western edge of
the Russian breeding area, reserves exist
but are not currently planned for
development in the Laptev formation on
the arctic coast east of the Lena River
(USGS 2007, pp. 1–2).
We are not aware of any yellow-billed
loon surveys in the Taymyr, TimanPechora, and Yamal districts described
above; so we do not know whether or
to what extent yellow-billed loon
breeding habitat overlaps with zones of
industrial activity in this area. It is
possible that the reported potential
contraction at the western edge of the
yellow-billed loon’s range in Russia
(Red Data Book of the Russian
Federation 2001, p. 366) could have
resulted from the effects of resource
extraction in the region, but we have no
evidence for or against this possibility.
No data are available on potential effects
of disturbance on yellow-billed loons,
and we know of no special protection to
prevent disturbance of yellow-billed
loons or other nesting birds in Russian
oil fields (Syroechkovskiy 2008, p. 1).
Likewise, we have no information on
the possible impacts of oil spills, facility
development, and lake-water
withdrawals on yellow-billed loons in
Russia. Therefore, the remainder of this
section will focus on available
information regarding potential impacts
associated with oil and gas exploration
and development in Alaska.
The potential negative effects of
industrial development in yellow-billed
loon nesting areas includes disturbance
caused by aircraft, vehicular traffic,
heavy-equipment use, maintenance
activities, and pedestrian traffic.
Disturbance to nesting birds from oil
infrastructure has been widely
discussed but poorly documented (NRC
2003, p. 49; USDOI–BLM 2008a, pp. 4–
890, 4–891). Loons as a genus are
susceptible to disturbance, although
they sometimes habituate to predictable
disturbance (discussed in Vogel 1995,
pp. 15–18; Barr 1997, pp. 22–23; Evers
2004, pp. 35–37; Earnst 2004, pp. 19, 31;
Mills and Andres 2004, pp. 212–213;
North 1994, p. 16). Human disturbance
can cause yellow-billed loons to
abandon reproductive efforts or leave
eggs or chicks unattended and exposed
to predators or bad weather (Earnst
2004, p. 19). Observations by Earnst
(2004, p. 31) indicated that adults left
nests when an approaching human is as
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much as 1.6 km (1 mi) away, or as close
as a few meters (yards). These behaviors
varied by individual and circumstance,
and have not been subject to formal
study (Earnst 2004, p. 31); more
importantly, the impacts to fitness and
the potential for habituation have not
been studied. Preliminary observations
have been made on the Colville River
Delta, Alaska, where oil field
development has occurred in yellowbilled loon nesting habitat. Yellowbilled loons were surveyed during
nesting and brood-rearing before (1993,
1995–1997) and during (1998–2001) the
oil-facility-development phase; surveys
are continuing in the oil production
phase that began in 2000 (ABR Inc.
2007, pp. 1–2; Johnson et al. 2008, p. i).
Between 16 and 30 nests were identified
each year. No statistical comparisons
among phases are available, but the
proportion of territories with nests and
nest success appeared roughly
comparable before and during
construction and during production.
Too few pairs (3) have been within 1.6
km (1 mi) of facilities to allow
meaningful comparisons of potential
disturbance among phases (ABR 2007,
pp. 3–4).
Potential disturbance and other
habitat degradation on NPR–A oil fields
will likely be mitigated by stipulations
and required operating procedures
(ROPs) described in the RODs for the
Northwest and Northeast Planning
Areas and included in oil and gas leases
for those areas (USDOI–BLM 1998,
Appendix B, pp. 29–43; USDOI–BLM
2004a, Appendix B, pp. B–1–B–18;
USDOI–BLM 2008b, Appendix A, pp.
33–74). Most of the area leased is
subject to the performance-based
stipulations and ROPs described here;
for tracts leased in 1999 and 2002 under
the 1998 ROD, prescriptive stipulations
and ROPs apply (USDOI–BLM 1998,
Appendix B, pp. 29–43). When lessees
propose specific development plans for
those tracts, there will be opportunities
for the BLM to apply conservation
measures for yellow-billed loons, as
appropriate. For tracts leased under
more recent RODs (USDOI–BLM 2004a,
Appendix B, pp. B–1–B–18; USDOI–
BLM 2008b, Appendix A, pp. 33–74),
ROP E–11 requires facility setbacks from
lakes known to harbor nesting yellowbilled loons, and E–2 and K–2 require
smaller setbacks for other water bodies.
The current ROP E–11 states that if
yellow-billed loons are found during
required aerial surveys, design and
location of facilities must minimize
disturbance; default mitigation is a 1mile buffer around nest sites and a 500meter buffer around the remainder of
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the lake shoreline (USDOI–BLM 2004a,
Appendix B, p. B–9; USDOI–BLM
2008b, Appendix A, pp. 51–53). The
size of these buffers was determined in
consultation with the Service and loon
experts. Deviations to ROPs and
stipulations can be authorized if it is
demonstrated that the conservation
objective of the stipulation or ROP can
be met, or if it is determined that no
other options are available (USDOI–
BLM 2008b, Appendix A, pp. 52–53).
Such deviations are sometimes
exercised (e.g., USDOI–BLM 2004b, p.
1033), but BLM has committed in
writing to close collaboration with the
Service in its evaluation of a deviation
request that may affect yellow-billed
loons (V. Galterio, in litt. 2008, p. 1).
Specifically, BLM has stated in writing
that any exception or deviation would
be required to meet the management
objective of minimizing disturbance to
the species and would, at a minimum,
need to provide the same level of
protection that the default buffers
provide (V. Galterio, in litt. 2008, p. 2).
This and other ROPs and stipulations
are also discussed under Factor D.
Varner (2008a, pp. 1–4) analyzed the
likelihood that oil-field facilities placed
randomly (i.e., without regard to loon
distribution) on the landscape would
occur proximal to loon nesting or broodrearing areas. Using data from Stehn et
al. (2005, pp. 1–38) that identified lakes
within NPR–A leased tracts that have a
less than 30 percent likelihood of
yellow-billed loon presence (moderatehigh potential yellow-billed loon lakes)
and BLM’s projected development
scenarios for NW and NE NPR–A,
Varner (2008a, p. 4) estimated that 52
percent of 12 projected facilities would
occur within the 1.6 km (1 mi) buffer of
a moderate-high potential yellow-billed
loon lake, and 38 percent would occur
within a 500-m (1,640 ft) buffer. In other
words, approximately half of projected
developments would require additional
consideration during site layout and
design to avoid yellow-billed loon
buffers. We note that this development
projection is uncertain, and it is
possible that either a smaller or greater
number of facilities could actually be
built.
In summary, based on our
understanding of factors affecting nest
success in other species and our
knowledge of loon behavior, we have
identified potential impacts of
disturbance to loons in NPR–A.
However, the only data on the effect of
oil development disturbance on yellowbilled loons are from the Colville River
Delta, where small sample size and lack
of controls or replicates make inference
difficult. As suggested by Earnst (2004,
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p. 31), a well-designed study is needed
to determine the most appropriate buffer
distance between loon nesting lakes and
oil facilities. However, we believe that
current buffer distances are conservative
and will protect loons from disturbance.
We do not know how much
development will occur in NPR–A, nor
do we know the timeline over which
development will occur. In NPR–A,
where 90 percent of yellow-billed loons
breeding on the ACP occur, we expect
that adherence to current BLM
regulations will ameliorate impacts by
requiring that planners build facilities
outside buffers or find other ways to
comparably minimize disturbance.
Terrestrial oil or fuel spills occur
during oil and gas extraction activities
from multiple sources, including well
blowouts, pipeline leaks, failure of fuel
storage tanks, and accidents
transporting fuel. Spills of saline water
produced with oil or derived from
seawater used in oil recovery also occur
frequently (NRC 2003, pp. 47, 230).
Marine oil spills may damage prey
populations, and air and boat traffic
associated with oil and gas extraction
offshore could affect yellow-billed loon
habitat by disturbing loons so that they
decrease foraging success or avoid
disturbed areas. Both non-nesting and
breeding yellow-billed loons on
Alaska’s ACP use marine areas of the
Beaufort and Chukchi Seas to forage
during the nesting season. In addition,
in spring yellow-billed loons gather in
polynyas, ice leads, and open shorelines
near river deltas offshore of breeding
areas in Alaska and Canada prior to
dispersing to nesting grounds. Here we
discuss effects of spills on loon habitat;
direct effects of oil spills on loon
mortality are discussed under Factor E.
Negative effects are expected to result
for bird habitats contacted by oil spills
(USDOI–BLM 2008a, pp. 4–760, 4–916).
Changes in freshwater chemistry or
pollutant loads due to oil spills
associated with oil and gas development
could render breeding habitats
unsuitable (NRC 2003, pp. 6–7, 73–74).
Oil or saline water spills could have
long-term effects on tundra waters by
killing prey and shoreline vegetation
(NRC 2003, pp. 95, 119, 124–125, 230–
231; USDOI–BLM 2008a, pp. 4–914, 4–
915), thereby reducing food availability
and cover.
On Alaska’s North Slope oil fields,
one of the most closely regulated oil
production areas in the world, there
were 3,696 spills from oil production,
pipeline, and oil exploration facilities
between July 1995 and June 2005
totaling more than 6.8 million liters (L)
(1.8 million gal) of sea water, produced
water, crude and diesel oil, and drilling
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12941
muds (ADEC 2007, p. 49). Most spills
have been relatively small and caused
minimal impacts to surrounding
habitats or wildlife, although three
major spills have occurred from the
North Slope segment of the TransAlaska Pipeline (NRC 2003, p. 47), and
a transit pipeline accident spilled 6,357
barrels (bbl) of crude oil in 2006 (ADEC
2008, p. 1). It is difficult to predict the
likelihood of future spills, in part
because technology continues to
improve. Based on previous spill rates,
BLM estimates that development in NE
NPR–A could result in more than 2,000
small oil spills (less than 500 bbl), and
approximately 3 large spills (greater
than 500 bbl) (USDOI–BLM 2008a, pp.
4–60–4–62); in the next 100 years, there
is a 4.2 percent chance of a very large
(238,000 bbl, or 10-million-gal) blowout
oil spill in NPR–A (USDOI–BLM 2008a,
p. 4–910). If, as expected, development
is concentrated in specific areas that
overlap with high-density loon breeding
habitat, the potential for oil spills
affecting some loon nesting lakes exists.
However, as discussed above and under
Factor D, measures are in place in NPR–
A to lessen this potential. For example,
ROP E–11 requires minimizing
disturbance to loons using setbacks of
permanent infrastructure around nesting
lakes that would make spills less likely
to affect these lakes; other stipulations
and ROPs require minimizing the
potential for pipeline leaks and
protecting fish-bearing water bodies
(USDOI–BLM 2008b, Appendix A, pp.
33–74).
Construction of roads, gravel pads,
and facilities on the North Slope of
Alaska has affected freshwater flow and
drainage as a result of permafrost decay
consequent to infrastructure placement,
vegetation damage, or fluid extraction
and injection (NRC 2003, pp. 3, 10, 64–
72, 126–127). North (1994, p. 16) and
North and Ryan (1989, p. 303) suggested
that permafrost decay consequent to
infrastructure placement and
disturbance of vegetation could cause
breaching of rivers into yellow-billed
loon breeding lakes, rendering them
unsuitable due to fluctuating water
levels (causing drowned nests) or
increased turbidity (negatively affecting
foraging success). The requirement in
ROP E–11 of a 1.6 km (1 mi) buffer
around nest sites and a 500-meter (1600ft) buffer around the remainder of the
lake shoreline or an equally protective
alternative where no permanent
infrastructure would occur (USDOI–
BLM 2004a, Appendix B, p. B–9;
USDOI–BLM 2008b, Appendix A, pp.
51–53) will likely lessen the chances of
such damage. It is possible that ice
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roads on breeding lakes could compact
lake ice and delay melting (USDOI–BLM
1998, p. IV–3–b–1–b), thus delaying or
discouraging yellow-billed loon
breeding, since loons require lakes to be
largely clear of ice before they
commence nesting. There are currently
no regulations which would prevent ice
roads on breeding lakes.
It is possible that lake-water depletion
or drawdown could affect
connectedness, depth, or melt date of
yellow-billed loon nesting or broodrearing lakes and could render such
areas unsuitable as breeding habitats.
Fluctuations in lake water levels during
nesting could cause nests to flood, or
alternately could leave nests stranded
away from the water during incubation,
making them more vulnerable to
depredation or abandonment (e.g.,
Kertell 1996, pp. 356–366 for Pacific
loons; Fair 1979, pp. 57–63 for common
loons; see also discussion in Earnst
2004, p. 19). Earnst (2004, p. 19)
proposed that yellow-billed loons might
be less adapted to fluctuating water
levels than other loons, in part because
the short arctic summer does not allow
the opportunity to re-nest or delay nest
initiation. Water withdrawals could
have additional impacts on habitat
suitability by affecting fish populations
that breeding yellow-billed loons
depend upon for food.
Usually taken by pumping in winter,
water from lakes is used in arctic oil
fields for exploratory drilling, as well as
winter road and pad construction and
facility use. From 1999 through 2006,
approximately 2 billion L (513 million
gal) of water from 126 lakes were used
to drill 20 wells and construct 23 ice
drill pads and roads in the NW NPR–A
(USDOI–BLM 2008a, p. 3–26). During
development, water is needed for
drilling and facility use. According to
BLM, ‘‘Drilling water demand is
estimated to be 21,000 to 63,000 gal per
day, or 850,000 gal per well. Water
demand is estimated to be 100 gallons
per day per person. Potable water
demand would drop after 2 to 4 drilling
seasons, when the major construction
phase would be finished.
Approximately 160 persons would be
on site during the production and
development phases for each CPF
(central processing facility) and 4 to 6
satellite fields (S. Rothwell,
ConocoPhillips, pers. comm.). Drillingwater demand over the 20-year
production life of the field (largely for
workover operations and infill drilling)
would likely be less than the 21,000 gal
per day estimated above’’ (USDOI–BLM
2008a, p. 4–30).
During production, waterflooding
(injecting water into the reservoir) is
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sometimes used, but it is more costeffective to use treated sea water rather
than freshwater from lakes (Varner in
litt. 2008b, p. 1). BLM has included
potential use of lakes for waterflooding
in their consideration of environmental
effects of oil and gas development in
NPR–A (USDOI–BLM 2008a, pp. 4–31–
4–32), but at present such use is
considered unlikely, particularly
considering present stipulations and
ROPs protecting lake fish and wildlife
habitat (Varner in litt. 2008b, p. 1).
Injection water demands can be met by
produced formation water (i.e., water
within the pores of rock) once
production begins (Varner in litt. 2008b,
p. 1; USDOI–BLM 2008a, pp. 4–31–4–
32).
The actual amount of water
withdrawn from lakes is highly variable
and dependent upon the type of water
use. To build ice roads, the amount
taken from a given lake may be lower
than allowed limits because it is not
efficient to transport water a long
distance; in contrast, lakes used for
facility use or drilling are pumped more
frequently and throughout the year
(Hinzman et al. 2006, pp. 14, 56; Baker
Inc. 2007, p. 4; Moulton 2007, p. 11).
Most pumped lakes monitored by oil
companies on the ACP have recharged
completely in spring from snowmelt or
river flooding; however, most removals
were much less than the 30-percent
volume permitted at the time by State of
Alaska regulations (Hinzman et al. 2006,
p. 143; URS 2001, p. 4–1; Baker 2007,
pp. 77–79; Baker 2008, pp. 7, 38). Two
adjacent lakes monitored at Alpine
Development showed different patterns
in 2007: One recharged adequately from
estimated snowmelt runoff given the
allowable withdrawal volume of 30
percent; the other lake did not do so,
and would likely be below required
levels if river flooding did not occur
(Baker 2008, p. 38).
We examined whether current
regulations will likely be adequate to
protect loon nesting lakes from
excessive water withdrawal. Ninety
percent of yellow-billed loon nesting
range on the ACP is under BLM
management in NPR–A. Outside NPR–
A, the Alpine development on the
Colville River Delta is the only set of oil
facilities in ACP yellow-billed loon
nesting range under sole State of Alaska
management. At this facility, the State
increased the 15-percent limit on water
withdrawal from one lake with nesting
yellow-billed loons to 30 percent
because ‘‘the previous criterion imposed
a severe constraint on the project’’
(Moulton 2007, p. 4). However, since
that decision, the State of Alaska has
participated in the ‘‘Conservation
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Agreement for the Yellow-billed Loon
(Gavia adamsii),’’ making a commitment
to protect yellow-billed loons
(Conservation Agreement 2006, p. 11)
and, therefore, making it less likely that
the State would allow such activities to
occur if they might negatively affect
loons.
In NPR–A, water-withdrawal
stipulations and ROPs are specifically
designed to protect and monitor fishbearing lakes. The current Federal
(BLM) requirements for NE NPR–A,
based on State of Alaska permit
regulations, allow up to 15 percent of
lake volume below ice cover to be
removed from lakes deeper than 2.1 m
(7 ft) with ‘‘sensitive’’ fish species (i.e.,
fish other than ninespine stickleback
and Alaska blackfish) and up to 30
percent of lake volume from lakes
deeper than 1.5 m (5 ft) with nonsensitive fish species; up to 35 percent
may be removed from lakes without fish
(USDOI–BLM 2008b, Appendix A, pp.
44–45). Permits are based on a sitespecific analysis. At present, there are
no requirements to prevent pumping of
known loon-nesting lakes, and no
requirements for direct measurements of
effects on lake biota, including fish.
However, in a letter to the Service
emphasizing the BLM’s commitment to
supporting conservation of the yellowbilled loon, the BLM State Director for
Alaska expressly clarified the ROPs and
stipulations in NPR–A leases
concerning water withdrawal.
Underscoring the importance of
continued collaboration with the
Service (V. Galterio, in litt. 2008, pp. 1–
3), the State Director explained that it
will require a water-quality monitoring
plan to be developed that will outline
specific physical and biological waterquality parameters to be collected in
lakes harboring yellow-billed loons (V.
Galterio, in litt. 2008, pp. 1–3). We
believe these requirements will protect
yellow-billed loon lakes from
deleterious effects of water withdrawals.
See discussion under Factor D,
Inadequacy of Existing Regulatory
Mechanisms.
In conclusion, we have identified
several mechanisms by which
development could affect yellow-billed
loons, including disturbance, oil spills,
facility development, and lake-water
withdrawals. Although we believe
onshore oil and gas activity is likely to
increase in Alaskan and Russian
breeding grounds in the foreseeable
future, we do not believe these activities
will result in significant populationlevel impacts. Although a large
proportion of high-density yellow-billed
loon nesting habitat on Alaska’s ACP
coincides with areas of high potential
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for oil and gas development in NPR–A,
the BLM, through stipulations and ROPs
required to be included in oil and gas
leases, has established a number of
mechanisms to protect yellow-billed
loons from the effects of oil and gas
activities in NPR–A, if development
ultimately does overlap with yellowbilled loon breeding habitat. We believe
that disturbance and spills will likely be
minimized through requirements that
facilities be built at least 1.6 km (1 mi)
from nests, and 500 m (1,640 ft) from
lake shorelines, or an equally protective
alternative. The BLM and the State of
Alaska have committed to work with the
Service to minimize impacts through
water quality monitoring. With current
projections of approximately 12
facilities in NPR–A, we believe the
current regulations and close
consultation with the Service are
sufficient to protect yellow-billed loons
from population-level effects of oil and
gas development on the ACP. Based on
the best available information we find
that oil and gas development in the ACP
is not a threat to the yellow-billed loon
now or in the foreseeable future.
On western Russian breeding
grounds, we do not have information on
whether yellow-billed loon distribution
overlaps with zones of industrial
activity. Due to lack of study, regulation,
and available information, the
environmental impacts of industrial
development in the Russian yellowbilled loon breeding range are not well
understood. Because the bulk of the
Russian breeding population appears to
occur in eastern Siberia (Yakutia and
Chukotka), where little industrial
development is occurring or planned,
most potential impacts of industrial
development in Russia are limited to the
western edge of the range. Based on the
best available information, we find that
oil and gas development is not a threat
to the yellow-billed loon in its Russian
breeding range now or in the foreseeable
future.
We expect large spatial and temporal
variation in the level of oil and gas
development activities on yellow-billed
loon breeding habitat, but most such
habitat will remain undeveloped in the
foreseeable future. We do not expect
terrestrial oil and gas development to
occur in the Canadian breeding range,
and Russian oil and gas development is
likely to be confined to the western edge
of the breeding range there. In Alaska’s
NPR–A, some areas are likely to be
developed, particularly at the eastern
edge of NE NPR–A near the Alpine
development. In Alaska, we believe that
existing required protective measures
will protect the yellow-billed loon from
impacts of development. We find that
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degradation of breeding grounds
throughout its range from oil and gas
development is not a threat to the
yellow-billed loon now or in the
foreseeable future.
Temperate Marine Habitat: Degradation
of Marine Habitats in Migration and on
Wintering Grounds
The marine environment is clearly
important for yellow-billed loons, as
that is where they spend their first 3
years, and subsequently at least 8
months per year. Wintering areas along
the coast of Alaska and British
Columbia, Canada, are relatively
pristine. Two important wintering areas
for yellow-billed loons, the western
Pacific Ocean coastal waters of the
Yellow Sea and Sea of Japan, and the
North and Norwegian Seas, have
recently been identified among the
ocean ecosystems with the greatest
human impacts, and therefore
degradation, of any in the world
(Halpern et al. 2008, p. 949). Possible
effects of human activities on yellowbilled loon marine migrating and
wintering habitats include depletion of
the prey base through a variety of
mechanisms, including pollutioninduced hypoxia and destructive fishing
practices, as discussed below. Potential
effects on loons from depletion of the
winter prey base include reduced body
condition, which could result in
mortality or reduced breeding
propensity.
Effects of marine oil spills, other
effects of marine oil and gas
development, and potential direct
effects of contaminants on yellow-billed
loons are discussed under Factor E.
Asian seas, where 24 out of 29 Alaskabreeding yellow-billed loons with
satellite transmitters wintered (Schmutz
in litt. 2008, p. 11), are undergoing
environmental stress. The United
Nations Global International Waters
Assessment (GIWA) Regional
Assessment of the Yellow Sea described
Yellow Sea fisheries as threatened by
‘‘pollution and loss of biomass,
biodiversity and habitat, resulting from
extensive economic development in the
coastal zone’’ (Teng et al. 2005, p. 33),
caused by a tenth of the world’s humans
(approximately 600 million) living in
surrounding watersheds. For example,
the East China Sea (adjacent to the
Yellow Sea) is undergoing ‘‘severe
environmental degradation’’ from inputs
of inorganic nitrogen, phosphate, oil
hydrocarbons, organic matter, and
heavy metals (Li and Daler 2004, p.
107). A significant effect of pollution
inputs in aquatic systems are zones of
eutrophication-induced hypoxia (‘‘dead
zones’’), which are among the most
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deleterious anthropogenic influences on
marine environments, leading to mass
mortality of fish and invertebrates, and
major changes in community structure
(Diaz and Rosenberg 2008, p. 926). Large
ecosystem effects of eutrophication and
hypoxia have been documented in
coastal waters of Japan (e.g., Ueda et al.
2000, pp. 906–913; Suzuki 2001, pp.
291–302; Kodama et al. 2002, pp. 303–
313), Korea (Lim et al. 2006, p. 1525),
and the East China Sea (Chen et al.
2007, p. 399). However, these effects are
seasonal, occurring more often in
summer, when adult breeding yellowbilled loons would have migrated from
the area. These effects also vary
geographically, with most severe dead
zones occurring at mouths of
watersheds with large population
centers or that deliver large quantities of
nutrients.
Unsustainable fishing practices,
including overfishing, indiscriminate
trawling, and use of pesticides for
fishing (Teng et al. 2005, pp. 34–35),
have resulted in significant changes in
the fisheries of the intensively exploited
Yellow Sea and other Asian fisheries.
These changes include significant
declines in fish populations and
changes in community structure, with
larger (and commercially important)
species replaced by smaller (and less
valuable) fish (Teng et al. 2005, p. 33).
Unsustainable exploitation of marine
natural resources is expected to
continue over the next 20 years, causing
fisheries production to decrease by 30–
50 percent (Teng et al. 2005, p. 35).
Degradation of temperate marine
wintering and migrating yellow-billed
loon habitats could deplete the yellowbilled loon prey base, which could
cause reduced body condition,
mortality, fewer birds migrating, and
reduced breeding propensity. Although
information exists regarding pollution
occurrence and effects on fisheries in
temperate marine waters in Asian
wintering areas, we do not know which
species yellow-billed loons eat there.
We therefore do not know whether
yellow-billed loon prey species have
been affected. Indeed, documented
changes in community structure from
large finfish to smaller forage fish could
benefit yellow-billed loons, as their diet
items are relatively small. Further,
although pollution and declines in
fisheries are documented in Asian
Pacific wintering areas, the information
is inadequate to assess what proportion
of the habitat or wintering loons is
affected. We also have no data on
yellow-billed loon mortality due to
habitat degradation in wintering areas or
migration routes, or on body condition
at any season.
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In summary, yellow-billed loon
mortality from marine pollution has not
been documented. The only other
source of information we have to
evaluate this factor is population trend
information from the ACP. Yellowbilled loons breeding on the ACP
migrate to Asian wintering grounds
(Schmutz in litt. 2008, p. 1). If
deterioration of these wintering areas
were resulting in population-level
effects on yellow-billed loons, we would
expect to see evidence of a large
population decline on the Alaska
breeding grounds. Instead, survey trends
indicate a slightly declining or stable
population. We do not have information
indicating that the current effects to the
species from the degradation of
temperate marine waters will change in
the future. Therefore, we find that
degradation of temperate marine waters
is not a threat to yellow-billed loons
now or in the foreseeable future.
PWALKER on PROD1PC71 with PROPOSALS2
Climate Change
While climate change impacts to some
environmental features (e.g., sea ice) can
be reliably assessed to some degree into
the future, assessment of climateinduced changes to yellow-billed loon
habitat in arctic terrestrial and
freshwater systems and arctic and
temperate marine systems is complex,
with highly variable predictions of
effects. Current models suggest that
global temperatures are likely to
continue to rise for up to 50 years, even
if greenhouse gas emissions were curbed
today (Meehl et al. 2007, p. 749). Below,
we evaluate the available information
on possible climate-change effects in
these systems that could affect yellowbilled loons.
I. Arctic Habitats
There is strong evidence of ongoing
impacts of climate change in the arctic,
all of which are predicted to continue or
accelerate in the next century (Anisimov
et al. 2007, pp. 662–663; Christensen et
al. 2007, pp. 902–903), although with
varying degrees of uncertainty and
regional variation (Reist et al. 2006b, p.
381) in effects on different biotic
communities, hydrology, and
geomorphology. Impacts include rising
air temperatures (Anisimov et al. 2001,
summarized in Anisimov et al. 2007, p.
656) at approximately twice the global
rate (McBean et al. 2005, p. 39),
declining summer sea ice (RichterMenge et al. 2008, p. 1), increasing
coastal erosion (Mars and Houseknecht
2007, p. 585; Rachold et al. 2002, cited
in Walsh et al. 2005, p. 233), rising sea
levels (Walsh et al. 2005, pp. 232–234),
a small increasing trend in precipitation
(McBean et al. 2005, p. 39), warming
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and thawing permafrost, and decreasing
extent of land underlain by permafrost
(Clow and Urban 2008, p. 3; Walsh et
al. 2005, p. 210; Jorgenson et al. 2006,
p. 1; Jorgenson et al. 2008, p. 1). All of
these could interact via feedback loops,
as described below.
With respect to the yellow-billed
loon, we are most concerned about
effects of potential climate-induced
changes on morphology of breeding
lakes and prey fish communities. In
northern areas, such as along the arctic
coast in most of the yellow-billed loon’s
breeding habitat (Siberia, Alaska’s ACP,
and most of the Canadian breeding
range), permafrost is continuous, and
could be hundreds of meters (ft) deep.
However, some habitat extends south of
this region to areas of discontinuous
permafrost, which is more susceptible to
the effects of climate change (Seward
Peninsula, southern part of the
Canadian range). Yellow-billed loon
breeding habitat on the arctic coast
depends on a unique hydrological
system, which is in turn dependent
upon cold temperatures resulting in
continuous and stable permafrost
underlying perched (i.e., isolated above
the groundwater) lakes (Rovansek et al.
1996, p. 316) and relatively consistent
weather patterns, such as most
precipitation deposited in winter as
snow, and spring ice-jams and floods
contributing to lake recharge (Prowse et
al. 2006, pp. 330–331). A community of
fish species has adapted to this system,
overwintering in deeper lakes, but also
entering or leaving some lakes during
spring river floods.
Morphology of Breeding Lakes
Permafrost thawing could reduce the
size, number, or suitability of lakes that
yellow-billed loons use for nesting and
brood-rearing, especially near the
southern boundary of continuous and
discontinuous permafrost. When nearsurface permafrost thaws, unfrozen
channels develop between and below
water bodies, allowing subsurface
drainage to occur. In addition,
permafrost degradation around edges of
lakes near river channels can cause
lakes to be breached and drained (Mars
and Houseknecht 2007, p. 586).
Permafrost degradation has already
affected lakes in some areas at the
southern boundary of continuous
permafrost. In Siberia, L.C. Smith et al.
(2005, p.1) documented a decline in
lake abundance and area in zones of
discontinuous permafrost. Yoshikawa
and Hinzman (2003, p. 151)
documented numerous shrinking ponds
on Alaska’s Seward Peninsula, at the
southern boundary of the yellow-billed
loon’s range, due to an increase in
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internal drainage following permafrost
degradation between 1950 and 2000.
Because a limited number of loon
surveys have been conducted on the
Seward Peninsula, we do not know
whether these changes are affecting
yellow-billed loons there. Riordan et al.
(2006, p. 1) observed ponds shrinking
throughout subarctic Alaska, and
attributed this drying to permafrost
warming, as well as increased
evaporation during a warmer and longer
growing season. The arctic zone of
continuous permafrost has relatively
cold air temperatures and is considered
relatively stable. However, Clow and
Urban (2008, p. 3) measured increases
for a total average warming of 3.5 K
(kelvin) (3.5 degrees C, 6.3 degrees F)
during 1989–2007, and Jorgenson et al.
(2006, p. 1) observed a recent, abrupt
increase in the extent and rate of ice
wedge degradation on Alaska’s ACP. Ice
wedges are 2–4 m deep polygons of ice,
more than 3,000 years old, occurring
just below the vegetation layer in icerich regions of the arctic. Both effects
were coincident with record warm air
temperatures in the late 1990s.
Permafrost warming and thawing is
predicted to continue as the arctic
climate warms (Meehl et al. 2007, p.
772). Zhang et al. (2007, p. 443)
simulated changes in Canada’s
permafrost distribution using a model
driven by six general circulation
models. They predicted that active layer
(the top layer of soil that thaws in
summer) thickness would increase, the
boundary between continuous and
discontinuous permafrost would move
north, and there would be significant
impacts on surface and ground
hydrology. Stendel et al. (2007, pp. 203,
211) used a high-resolution regional
climate model to predict changes to
permafrost in eastern Siberia over the
next century, and concluded that under
the various modeling scenarios
reviewed by the Intergovernmental
Panel on Climate Change (IPCC), the
active layer depth would increase up to
1 m (3.1 ft) along the arctic coast. These
predictions suggest that some breeding
lakes, particularly in the southern part
of the yellow-billed loon’s range, could
be altered, but overall effects will
depend on the magnitude and direction
of other changes (e.g., precipitation).
Arctic sea-ice loss accelerates air
temperature warming, which, in turn,
increases permafrost warming. Recently,
Lawrence et al. (2008, p. 1) evaluated
how periods of abrupt rapid sea-ice loss
affect terrestrial arctic climate and
ground thermal state in the Community
Climate System Model. They found that
arctic land warming trends would be 3.5
times greater during periods of rapid
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sea-ice loss than otherwise predicted for
the 21st century. They predicted that
such a warming period would increase
ground heat accumulation substantially,
increasing the vulnerability of
permafrost to degradation (Lawrence et
al. 2008, p. 1). The 2007 arctic summer
sea-ice extent was a new record
minimum since satellite measurements
began in 1979, with a large reduction in
area compared to the previous record set
in 2005 (Richter-Menge et al. 2008, p. 1),
and the 2008 extent was similar
(National Snow and Ice Data Center,
https://nsidc.org/data/seaice_index/
index.html).
Aside from causing increased land
warming trends, loss of sea ice could
affect freshwater breeding lakes adjacent
to marine shorelines through breaching
and increased salinity, because
shorelines would no longer be protected
from storms by summer and fall
shorefast ice (Mars and Houseknecht
2007, p. 586). Coastal erosion rates are
increasing, with land loss rates in some
of Alaska doubling in the last half
century (Mars and Houseknecht 2007, p.
585), and parts of the Laptev Sea coast
in arctic Russia are retreating at an
average rate of 2.5 m (8.2 ft) per year
(Rachold et al. 2002, cited in Walsh et
al. 2005, p. 233), but it is not known
whether yellow-billed loon breeding
lakes in this region are close enough to
the coast to be affected. These effects are
exacerbated by rising global sea levels.
The greatest sea-level increases over the
next century are projected for the arctic,
although with much uncertainty
(Christensen et al. 2007, p. 914; Walsh
et al. 2005, pp. 232–234).
The amount and timing of
precipitation also influences the
permafrost active layer, and is predicted
to increase in the arctic (Christensen et
al. 2007, pp. 902–906), with a greater
percentage increase in winter and less
in summer. Increased snow cover in
winter is likely to contribute to
permafrost warming, as snow limits heat
exchange between the atmosphere and
the ground; significant snow cover
keeps the ground warmer than the air
(Stieglitz et al. 2003, p. 1). Predicted
increased frequency of rain-on-snow
events in Alaska and eastern Siberia
(Rennert et al. 2008, p. 4) would
exacerbate the warming effect on
permafrost, as latent heat release from a
single large rain-on-snow event can
constrain the soil temperature to 0
degrees C (32 degrees F) for months
(Putkonen and Roe 2002, p. 1,188).
There could also be direct effects of
changes in precipitation on lakes used
by yellow-billed loons. Increased winter
precipitation could provide more spring
floodwater to recharge lake basins
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(Walsh et al. 2005, p. 188; Prowse 2006,
pp. 330–331). In contrast, increased
summer rainfall will likely be lost to
stream flow, increased subsurface
storage, and increased evaporation in
warmer air temperatures (Rovansek et
al. 1996, p. 311; Bowling et al. 2003, p.
2–1). Earlier snow melt from increasing
air temperatures and the predicted
increase in winter rain events could
decrease large breakup events in the
spring, perhaps reducing lake
replenishment from ice-jam flooding.
Overall, it is possible that lakes at the
southern boundary of continuous
permafrost could be affected, that this
boundary will move north, and that
eventually even northern areas of
continuous permafrost could experience
changes that will negatively affect lakes.
For the yellow-billed loons, these effects
could mean reduced habitat in the
southern part of its range in the nearterm (an uncertain period, but perhaps
the next several decades), and
eventually, in the northern parts of its
range. At present, however, models have
not been developed to make reliable
predictions about the timing or extent of
such habitat reductions and associated
impacts on the species. Although
permafrost degradation has already
occurred in southern parts of the
breeding range, such as the Seward
Peninsula, there have been no observed
effects on loon breeding lakes, and we
do not have trend information for that
population (which could provide some
indication of the population impacts of
permafrost degradation). Therefore,
based on currently available information
we find that climate-induced changes to
the morphology of the yellow-billed
loon’s breeding lake habitats are not a
threat to the species now, and we
cannot reasonably predict that they will
become a threat to the species in the
future.
Prey Fish Communities
Climate change could alter yellowbilled loon prey fish communities in
breeding lakes; species potentially
affected include ninespine sticklebacks,
Alaska blackfish, and least cisco
(considered among the most vulnerable
to extirpation through changes in
species composition) (Wrona et al. 2006,
p. 413). We are uncertain, however,
about the form or timing that potential
effects on fish communities might have
on yellow-billed loons due to the
interaction of factors influencing
community composition. Fish species
vary with lake depth and resulting ice
thickness. Shallow (less than 2 m) (less
than 6.6 ft) lakes that freeze to the
bottom cannot harbor overwintering
fish, and even somewhat deeper lakes
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may have low dissolved oxygen levels,
allowing only species adapted to these
low levels, such as sticklebacks and
Alaska blackfish, to survive. Shallow
lakes that freeze to the bottom
sometimes maintain fish populations
via replenishment from spring river
floods. If ice thickness declines in a
warmer climate, deep lakes could have
increased oxygen, allowing less tolerant
species to overwinter, and shallower
lakes would be able to harbor
overwintering fish. Conversely, shallow
lakes might lose replenishment with
decreased spring flooding (Hershey et
al. 2005, pp. 39, 52). Fish habitat is also
dependent on basin shape, since
shallow littoral zones are needed to
provide food for fish; lower water levels
might alter or diminish littoral habitats.
Fish habitat characteristics are reflected
in yellow-billed loon habitat preferences
modeled by Earnst et al. (2006). Loons
were found more often on medium or
deep lakes than on shallow (less than 2
m) (less than 6.6 ft) lakes that freeze to
the bottom, and for shallow lakes, loons
were more likely to be present if the
lake was connected to streams or other
lakes. Proportion of shoreline with
vegetation, indicating littoral habitat,
was a positive indicator of yellow-billed
loon presence. Loons preferred both 2 to
4 m (6.6 to 13.1 ft) deep lakes and
greater than 4 m (greater than 13.1 ft)
deep lakes, but because the latter are
rare on the North Slope, 64 percent of
yellow-billed loon sightings were on
lakes 2 to 4 m (6.6 to 13.1 ft) deep
(Earnst et al. 2006, p. 235). In summary,
although climate change could have
negative effects on prey communities,
there could be positive effects. Not only
is there considerable uncertainty as to
the possible effects to prey communities
from climate change, there is also
substantial uncertainty about the timing
over which changes will occur.
Scientists have not yet developed the
specific predictive models and
empirical research to improve our
understanding of these changes and
enable us to predict the timing with
which they might occur.
In addition to breeding lakes, yellowbilled loons in summer use shallow
nearshore marine waters (less than 10 m
(33 ft), roughly within 20 km (12.4 mi)
of shore) adjacent to mainland habitats
and near barrier islands (Earnst 2004, p.
7). Little is known about the prey
species that yellow-billed loons use in
these habitats, although they are known
to eat a variety of species in winter
marine habitats (see Feeding Habits,
above; also reviewed in North 1994, p.
7 and Earnst 2004, pp. 9–10). Changes
in arctic marine ecosystems, including
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increased primary production,
introduction of new species, and
population shifts in existing species
could occur as the climate warms (Perry
et al. 2005, p. 1,912; Behrenfeld et al.
2006, p. 752; Reist et al. 2006a, pp. 370–
380). These changes to summer marine
prey communities would be complex,
and the form of potential new species
assemblages cannot be reliably
predicted at this time.
Increased ocean acidification as a
result of increasing levels of
atmospheric carbon dioxide could affect
marine food webs, but the form,
magnitude, and timing of such effects
are unknown. Due to limited research
and understanding of the processes
involved (Zeebe et al. 2008, p. 52), it is
not possible to predict effects on loon
prey species from ocean acidification at
this time.
Therefore, as discussed above, due to
a paucity of information and models
available to reliably predict effects of
climate-induced changes to yellowbilled loon prey species assemblages in
breeding lake and marine habitats, we
find that climate-induced changes to
yellow-billed loon prey species is not a
threat to this species now or in the
foreseeable future.
PWALKER on PROD1PC71 with PROPOSALS2
Polynyas and Ice Leads
We also considered whether polynyas
and ice leads, both of which provide
feeding and staging areas for yellowbilled loons in spring before the
breeding season, were likely to
disappear as the arctic climate changes.
Arctic sea ice is projected to decline
most, and surface air temperatures
increase most, in summer and fall
(Walsh 2008, p. S19). In 2007, there was
a record sea-ice minimum in the arctic
in September, and the Chukchi Sea did
not freeze until early December, but an
advancing ice field covered most of the
eastern Bering Sea shelf by mid-January
2008. A subsequent near record
maximum ice extent occurred in March
2008, and the Bering Sea was not ice
free until almost July 2008 (Overland
and Stabenow 2008, p. 2). Overland and
Stabenow (2008, p. 5) predicted that
although arctic sea ice will continue to
decrease seasonally in late summer and
fall, sea ice will still form in winter,
extending south to the Bering Sea. If this
projection is correct, polynyas and ice
leads should continue to provide
productive spring habitat for yellowbilled loons, even as the arctic climate
continues to warm. Therefore, we find
that loss of polynyas and ice lead
habitats is not a threat to yellow-billed
loons now or in the foreseeable future.
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Shipping Traffic
We also evaluated the potential effects
of increased disturbance and oil spills to
arctic yellow-billed loon habitat from
increased shipping traffic, as a result of
summer and autumn sea-ice loss,
throughout arctic marine waters near
loon breeding areas. Because of the seaice decline discussed above, in 2008
both the Northwest passage and the socalled Northeast Passage, or Northern
Sea Route, along the Russian arctic coast
were ice free likely for the first time
since the last ice age 125,000 years ago
(NSIDC 2008). As the extent of arctic sea
ice in the summer has declined and the
duration of ice-free periods has
increased, interest in shipping within
and through arctic waters has increased
(Brigham and Ellis 2004, p. 2). This
potential increase in shipping could
affect yellow-billed loons through
habitat degradation, disturbance, or fuel
spills. However, we have not found any
reliable predictions about the location,
type, and amount of shipping that might
occur as ice-free periods increase. In
addition, the wide distribution and low
density of yellow-billed loons in arctic
marine areas during the breeding season
makes it unlikely that the population
would be at increased risk if shipping
traffic were to increase. Because we are
uncertain about the magnitude of
shipping traffic increases and because
the low density of loons in the
environment makes them less
vulnerable to vessel accidents or
disturbance, we find that increased
arctic shipping is not a threat to yellowbilled loons now or in the foreseeable
future.
In summary, our evaluation of
climate-change effects on arctic yellowbilled loon habitats included
documented and predicted climateinduced changes to various features of
the environment, followed by
hypothetical but reasonable
suppositions about possible alterations
to habitats important to yellow-billed
loons. There are no data to suggest that
climate-induced changes documented to
date have resulted in breeding-habitat
changes, and based on the stable or
slightly declining trend on the ACP, it
does not appear that these changes have
affected the yellow-billed loon
population there. At this time, we are
unable to predict potential future
changes to yellow-billed loons and their
habitats discussed above, because, in
addition to uncertainty about the
magnitude, direction, and timing of
climate-induced changes to the
environment, no empirical data exist
regarding the effects of those potential
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changes on yellow-billed loons or their
habitats.
In arctic areas, there is strong
evidence that coastal erosion is
occurring, and some evidence for
breaching of freshwater lakes adjacent to
coasts, but little or no information on
whether these environmental changes
have affected yellow-billed loon
breeding lakes. While there is strong
evidence that climate change is causing
permafrost loss, no information is
available on how this could affect
freshwater lake morphology and the
yellow-billed loon prey base in the
future. Based on the best available data,
we believe that important polynyas and
ice-lead spring staging habitat are likely
to continue to exist in the foreseeable
future. While ocean acidification will
likely have long-term effects on marine
communities, we do not know how it
will affect loons. We believe the effects
of increased shipping in arctic seas will
be negligible because yellow-billed
loons are widely dispersed across
breeding and migrating landscapes.
II. Temperate Habitats
Global ocean temperatures increased
(0.1 degrees C (0.2 degrees F) from 1961
to 2003, although with some cooling
since 2003; Bindoff et al. 2007, p. 387),
and effects on primary productivity and
dissolved oxygen varied with latitude.
Primary productivity in warm, lowlatitude oceans declines as upper-ocean
temperature increases, while warmer
temperature at high latitudes increases
productivity and decreases oxygen
levels (Behrenfeld et al. 2006, p. 752;
Bindoff et al. 2007, p. 400).
For the yellow-billed loon wintering
at low latitudes in the Yellow Sea and
the Japan (East) Sea, a drop in primary
productivity might mean decreased prey
availability. However, as already
observed in northern environments (e.g.,
Perry et al. 2005, pp. 1,912–1,915),
marine animals, including yellow-billed
loons, might shift north to colder, more
productive waters if winter sea ice is not
a barrier. As noted for northern marine
species (e.g., Perry et al. 2005, p. 1,914)
the movements of species as a result of
climate change will likely be complex,
so predicting the form of new species
assemblages is difficult.
Potential expansion of oxygendeficient ‘‘dead zones’’ in Asian coastal
waters where yellow-billed loons winter
depends partly on how climate change
affects water-column stratification (Diaz
and Rosenberg 2008, p. 929). Warming
ocean temperatures could increase
stratification, deepening the depletion
of oxygen, but increased storminess,
such as hurricanes, could increase
mixing and thereby lessen stratification.
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Changes in rainfall patterns could
change freshwater and nutrient inputs.
At this time, available data on the
effects of climate change on dead zones
in winter marine habitats of the yellowbilled loon are uncertain.
In summary, climate change effects on
the temperate-latitude wintering habitat
of the yellow-billed loon include
increases in ocean temperature and
decreases in primary productivity and
dissolved oxygen levels, which could
potentially affect prey fish communities
and their distribution. The magnitude
and form of these effects are highly
uncertain, but would most likely
involve a northward shift of prey
species, which could be mirrored by
their predators, such as wintering
yellow-billed loons. Therefore, while we
conclude that the effects of climate
change will be widespread and will
likely have some impact on yellowbilled loons in temperate habitats, we
find that climate-induced changes in the
temperate marine habitat are not a threat
to the yellow-billed loon now or in the
foreseeable future.
There are multiple hypothetical
mechanisms associated with climate
change that could affect loons and their
breeding and non-breeding habitats.
Unlike documented and predicted
declines in sea ice, an obligate habitat
for other arctic species such as polar
bears (Ursus maritimus), we lack
predictive models on how climate
change will affect yellow-billed loon
terrestrial, freshwater, and marine
habitats. Manifestations of climatemediated changes throughout arctic and
temperate yellow-billed loon habitats
will emerge as models continue to be
refined and effects are documented, but
at this time the timing, magnitude, and
net effect of the impacts are uncertain.
In our analysis of Factor A, we
identified and evaluated the risks to the
yellow-billed loon’s habitats, including:
Oil and gas development (i.e.,
disturbance, changes in freshwater
chemistry and pollutant loads, and
changes in freshwater hydrology);
pollution; overfishing; and climate
change. Based on our review of the best
available information, we find that the
present or threatened destruction,
modification, or curtailment of the
yellow-billed loon’s habitat or range is
not a threat to the species now or in the
foreseeable future.
Factor B: Overutilization for
Commercial, Recreational, Scientific, or
Educational Purposes
Subsistence harvest, as well as,
bycatch of loons during commercial and
subsistence fishing are discussed under
Factor E.
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Researchers seeking to understand the
life history of yellow-billed loons have
implanted 29 yellow-billed loons with
satellite transmitters to date (19 birds on
the ACP and 10 birds on the Seward
Peninsula, Alaska; Schmutz in litt.
2008). This research is permitted by the
Service under the Migratory Bird Treaty
Act (MBTA) and by the Alaska
Department of Fish and Game (ADFG)
under State law. Although it is
reasonably likely that there could be
heightened risks of mortality and
reduced productivity in individual birds
implanted with transmitters, the
number of loons in this study is not
sufficient to cause population-level
effects.
We do not have any evidence of risks
to yellow-billed loons from
overutilization for commercial,
recreational, scientific, or educational
purposes, and we have no reason to
believe this factor will become a threat
to the species in the future. Therefore,
we find that overutilization for
commercial, recreational, scientific or
educational purposes is not a threat to
the yellow-billed loon now or in the
foreseeable future.
Factor C: Disease or Predation
Loons are susceptible to avian
diseases, including avian cholera (from
Pasteurella multocida), aspergillosis
(from Aspergillus fumigatus), and avian
botulism (from Clostridium botulinum)
(Friend and Franson 1999, pp. 79, 130,
274), but we are not aware of any large
disease-related die-offs in yellow-billed
loons. Loons are susceptible to avian
influenza, but in Alaska, none of six
loons sampled, including two yellowbilled loons, tested positive for avian
influenza viruses in 2006 (USFWS/
USGS 2007, pp. 1–93; Y. Gillies in litt.
2008, p. 1), and worldwide the highly
pathogenic H5N1 has not been detected
in loons (https://www.who.int/csr/
disease/avian_influenza/en/, accessed
11/24/2008).
Predation on adult yellow-billed
loons is thought to be uncommon, but
predation on nests on the ACP has been
attributed as the primary cause of egg
loss and therefore reduced productivity
in some years (Earnst 2004, p. 22).
Yellow-billed loon nest predators
include glaucous gull (Larus
hyperboreus), parasitic jaeger
(Stercorarius parasiticus), and arctic fox
(Alopex lagopus); pomarine jaeger
(Stercorarius pomarinus), common
raven (Corvus corax), snowy owl
(Nyctea scandiaca), red fox (Vulpes
fulva), and grizzly bear (Ursus arctos
horribilis) also predate nests (North
1994, p. 11; Earnst 2004, p. 22). Many
of these predators are attracted to
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infrastructure, which is used as nesting
platforms or is associated with food
sources, and so predation might be
expected to increase as development in
yellow-billed loon nesting habitat
increases (NRC 2003, p. 6; Earnst 2004,
p. 19). However, in Alaska, NPR–A ROP
A–2 and A–8 require control of waste
and other measures to prevent attracting
wildlife to infrastructure (USDOI–BLM
2008b, Appendix A, pp. 37, 41–42),
reducing the risks associated with future
development. We do not know whether
similar regulations would be
implemented in Canada should
development occur there. The extent of
infrastructure increase in Russian
yellow-billed loon nesting habitats, and
accompanying regulation, is unknown.
In conclusion, we note that no large
disease-related mortality events have
been documented for yellow-billed
loons. Indeed, yellow-billed loons might
be relatively protected from avian
disease mass mortality events that are
more common in other water birds
because of the loon’s dispersed
distribution and relatively solitary
habits. We have no reason to believe
that disease outbreaks will increase or
will have more severe effects on yellowbilled loons in the future. Nest
predation might affect current
productivity, but population-level
effects are more likely to results from
decreases in adult survival (see
Population Resiliency, above).
Moreover, due to regulations associated
with infrastructure development that
also target increasing human safety, we
believe that nest predation is unlikely to
cause population-level effects in the
future, at least in Alaska and Canada; no
information is available that would
indicate future effects of such
development in Russia. Therefore, we
find that neither disease nor predation
is a threat to the yellow-billed loon now
or in the foreseeable future.
Factor D: Inadequacy of Existing
Regulatory Mechanisms
To determine if existing regulatory
mechanisms protect yellow-billed loons,
we evaluated existing international and
United States conventions, agreements,
and laws for the specific protection of
yellow-billed loons or their marine and
terrestrial habitats in the countries
where yellow-billed loons winter,
migrate, or breed. In July 2008, we sent
letters to national wildlife or natural
resource agencies in Canada, China,
Japan, North Korea, Norway, Republic
of Korea (South Korea), and the Russian
Federation, asking for information about
ongoing management measures and any
conservation and management strategies
being developed to protect the species.
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We received a formal response from the
government of Canada, and an informal
response from a government biologist in
the Russian Federation (discussed
below).
The yellow-billed loon is included in
the 2008 International Union for the
Conservation of Nature (IUCN) Red List
Category as a ‘‘Least concern’’ species;
widespread and abundant taxa are
included in this category. The species is
not currently listed under the
Convention on International Trade in
Endangered Species of Wild Fauna and
Flora (CITES); and trade is not known
to negatively affect the yellow-billed
loon. The species is listed under the
United Nations Environment Program
Convention on the Conservation of
Migratory Species of Wild Animals
(UNEP–CMS), although the United
States, Russia, Canada, and most Asian
nations are not signatories (https://
www.cms.int/, accessed September 9,
2008).
In Asia, no specific relevant laws for
North Korea or the Republic of Korea
(South Korea) were found that would
apply to protection of yellow-billed
loons or their habitat. Chinese wildlife
laws (The Law of the People’s Republic
of China on the Protection of Wildlife
1991; The Regulations for the
Implementation of the People’s
Republic of China on the Protection of
Terrestrial Wildlife 1992) protect
species of wildlife and the environment,
with provisions for hunting (including
licensure), and habitat protection for
species under the special protection of
the state, although the yellow-billed
loon is listed as ‘‘not threatened’’ by the
China Species Information Service
(CSIS database, https://
www.chinabiodiversity.com; accessed
Sept. 8, 2008).
The Japan-United States Convention
for the Protection of Migratory Birds and
Birds in Danger of Extinction, and Their
Environment (1974) includes the
yellow-billed loon, though it is not
designated as a Japanese endangered
species. The Convention prohibits the
taking of migratory birds or their eggs,
unless there are permitted exceptions
for subsistence. The Convention also
specifies that each party shall seek
means to prevent damage to such birds
and their environment, including,
especially, damage resulting from
pollution of the seas.
Lack of regulation and enforcement of
fishing and pollution in marine waters
of China and the Republic of Korea have
been identified as barriers to recovery of
the Yellow Sea ecosystem (UNDP/GEF
2007, pp. 79–84). ‘‘In the Yellow Sea,
there are clearly deficiencies in fisheries
management and regulation.
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Furthermore, these deficiencies have
contributed to environmental impacts or
threats to biodiversity in sectors other
than fisheries management’’ (UNDP/
GEF 2007, p. 80). We are concerned that
these problems could cause harm to
yellow-billed loons, but currently we
have little information on mortality
rates or loss of loon habitat in this
region, and no evidence from our
limited information on breeding
population trends indicates that the lack
of regulation in Asian waters is causing
a population-level threat to yellowbilled loons.
We received a response to our letter
to the Russian Ministry of Natural
Resources from the Russian Academy of
Sciences, which stated that there are no
ongoing management measures to
protect the yellow-billed loon in Russia.
They stated that all the best known
species’ breeding sites are outside any
protected areas, and no conservation
and management strategies have been
recently developed to protect the
species (E. Syreochkovskiy, Russian
Academy of Sciences, in litt. 2008).
The yellow-billed loon is listed in the
Red Data Book of the Russian
Federation (2001, pp. 366–367) as a
category 3 species (rare, sporadically
distributed species). The species is
nominally protected under the 1978
U.S. Migratory Bird Treaty with the
former Soviet Union (Convention
between the United States of America
and the Union of Soviet Socialist
Republics Concerning the Conservation
of Migratory Birds and their
Environment; Pub. L. 95–616), which
specifies that each party shall prohibit
the taking of migratory birds, the
collection of their nests and eggs, and
the disturbance of nesting colonies.
Exceptions include subsistence
purposes for indigenous people. The
Treaty also mandates that to the extent
possible, the parties shall undertake
measures necessary to protect and
enhance the environment of migratory
birds and to prevent and abate the
pollution or detrimental alteration of
that environment. Regional protection
occurs in some regions where yellowbilled loons occur such as Kamchatka,
Murmansk, Sakhalin, and Yamal-Nenets
Autonomous District (AD), but not in
Yakutia, Taymyr AD, or Chukotka AD,
where nesting is concentrated (Red Data
Book Bulletin 2003, p. 77). In
Kamchatka, yellow-billed loons are
protected in some nature reserves along
the eastern and southern coasts of
Kamchatka (Red Data Book of
Kamchatka, p. 92), but not along the
western coast where oil and gas
development are planned. Yellow-billed
loons are also protected under bilateral
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agreements between the Russian
Federation and the Korean Republic,
and Japan and China, respectively (Red
Data Book of Kamchatka 2006, p. 92).
We do not have reliable information on
enforcement of regulations in Russia,
and we also do not have information
that insufficient regulation or
enforcement has caused a populationlevel threat to the yellow-billed loon.
The Wildlife Act of Norway (1981),
where loons winter in marine waters,
specifies that all wildlife, including
eggs, nests, and habitats, are protected
(meaning that individuals of the species
may not be collected or destroyed)
unless otherwise prescribed by statutory
law. Norway’s marine ecosystem is
managed by the Ministries of
Environment, Fisheries and Coastal
Affairs, Petroleum and Energy, and
Labour and Social Inclusion (Royal
Norwegian Ministry of the Environment
2006, pp. 46–59), which coordinate
environmental laws regulating fishing
and controlling pollution from
development and vessel traffic (Royal
Norwegian Ministry of the Environment
2006, p. 46). We do not have evidence
that lack of adequate regulation in
Norway has or is likely to lead to threats
to the yellow-billed loon.
The yellow-billed loon is designated
as ‘‘not at risk’’ under Canada’s Species
at Risk Act of 2002, legislation similar
to the U.S. Endangered Species Act
(https://www.sararegistry.gc.ca/;
accessed January 28, 2009). In its
assessment and status report on the
yellow-billed loon, the Committee on
the Status of Endangered Wildlife in
Canada (COSEWIC) determined the
yellow-billed loon was ‘‘not at risk’’
(COSEWIC 1997, p. iii). The report
acknowledged that all loons are highly
susceptible to pollution and destruction
of wetland and coastal marine habitats
(COSEWIC 1997, p. vi). According to the
COSEWIC status report on the yellowbilled loon prepared by Barr (1997, p.
4), the dangers of human activities, the
naturally low population, limited
breeding habitat and food resources, and
inability to adapt ensure that the
yellow-billed loon will remain
vulnerable. However, he also stated that
its present low population could be
normal, stable, and well adapted to its
severe environment, and that there does
not yet seem to have been any
significant loss of critical habitat (Barr
1997, p. 4). The COSEWIC report (1997;
p. iii) concluded that the yellow-billed
loon is uncommon but widespread with
no evidence of declines or limiting
factors over widespread areas.
The Migratory Bird Treaty (or
Convention) between Canada and the
United States (originally ratified in 1916
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and implemented in 1918, and amended
in 1994 in Canada) established a legal
framework protecting migratory birds.
Under Canada’s Migratory Birds
Convention Act (1994), the Governor in
Council regulates migratory nongame
bird species, such as the yellow-billed
loon, by prohibiting the killing,
capturing, injuring, taking, or disturbing
of migratory birds or the damaging,
destroying, removing, or disturbing of
nests; prescribing protection areas for
migratory birds and nests; and requiring
the control and management of those
areas (https://laws.justice.gc.ca/en/
showtdm/cs/M-7.01///en; accessed
November 24, 2008). However, the Act
allows for the subsistence take of birds,
including the yellow-billed loon, by
Aboriginal people in Canada. Currently,
the species is not covered under
Canadian Provincial laws or regulations
and, thus, receives no additional
protections or conservation
considerations in Canada. There are no
conservation and management strategies
being developed to protect the species
in Canada (V. Poter, Canadian Wildlife
Service, in litt. 2008, p. 1), and no
population surveys are conducted or
planned. Although the two Migratory
Bird Sanctuaries where yellow-billed
loons breed (Queen Maud Gulf and
Banks Island Migratory Bird
Sanctuaries) encompass over 8 million
hectares total and are remote from major
human cities or other development,
subsistence hunting by Aboriginal
people is allowed within them
(MacDonald in litt. 2008, p. 1). At
present, we have some concern about
subsistence harvest in Canada which
appears to be unregulated, particularly
in light of the lack of knowledge about
loon population levels or trends, but we
do not have evidence that this lack of
regulation is causing a population-level
threat to the yellow-billed loon breeding
population in Canada.
Within the United States, the yellowbilled loon has protection under several
laws and regulations. The MBTA makes
it unlawful to kill or take eggs or nests
of yellow-billed loons, but it does not
provide protection for habitat, a
potential concern in relation to
development in breeding areas. Yellowbilled loons are not open for subsistence
hunting in Alaska under migratory bird
subsistence-harvest regulations (March
14, 2008, 73 FR 13788), but our analysis
of harvest surveys (discussed under
Factor E) indicates that harvest
nevertheless occurs, at times at
substantial levels. Although we have
some concerns about the accuracy of
reported harvest levels, as described in
Factor E, we have concluded that
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harvest is higher than previously
thought, and is likely unsustainable.
The yellow-billed loon is a K-selected,
long-lived species, that requires high
adult survival and has low recovery
potential and slow recovery rates once
populations decline; consequently,
significant mortality of yellow-billed
loons, especially of adults, is a major
concern. The Service and State of
Alaska have recognized the yellowbilled loon as a potentially vulnerable
species under the Birds of Conservation
Concern (68 FR 6179) and State
Comprehensive Wildlife Conservation
Strategy (https://www.sf.adfg.state.ak.us/
statewide/ngplan/, accessed September
9, 2008), respectively. These
designations provide management and
research funding prioritization.
Much of the yellow-billed loon’s
breeding range in Alaska is found on the
NW and NE NPR–A (which is managed
by the BLM), and the species is on the
BLM-Alaska’s list of sensitive species.
One of the objectives of BLM’s Special
Status Species Policy is to ensure that
actions requiring authorization or
approval by BLM are consistent with the
conservation needs of special status
species and do not contribute to the
need to list any special status species,
either under provisions of the Act or
other provisions of the policy.
Specifically, the BLM must manage the
habitat to conserve the species by:
ensuring sensitive species are
appropriately considered in land-use
plans; developing, cooperating with,
and implementing range-wide or sitespecific management plans,
conservation strategies, and assessments
for sensitive species that include
specific habitat and population
management objectives designed for
conservation, as well as management
strategies necessary to meet those
objectives; and ensuring that BLM
activities affecting the habitat of
sensitive species are carried out in a
manner that is consistent with the
objectives for managing those species.
The BLM has adopted stipulations
and ROPs for the NW and NE NPR–A
(USDOI–BLM 2004a, Appendix B, pp.
B–1–B–18; USDOI–BLM 2008b,
Appendix A, pp. 37–74) in order to
minimize potential impacts to yellowbilled loons, such as disturbance of
nesting birds and broods. As discussed
under Factor A, these include waterwithdrawal standards for deep fishbearing lakes and setbacks for
exploratory drilling and permanent
facilities near fish-bearing and deep
lakes (greater than 3.9 m (13 ft) deep).
Both the NW NPR–A Integrated Activity
Plan/Environmental Impact Statement
Record of Decision (USDOI–BLM 2004a,
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Appendix B, p. B–11) and the NE NPR–
A Supplemental Integrated Activity
Plan/Environmental Impact Statement
Record of Decision (USDOI–BLM 2008b,
Appendix A, pp. 51–53) contain ROP E–
11, an express objective of which is to
minimize disturbance to yellow-billed
loons from oil and gas activities in the
NPR–A (V. Galterio, BLM Alaska State
Director, in litt. 2008). This ROP
requires oil and gas lessees to conduct
multi-year surveys in order to detect
nesting yellow-billed loons before the
construction of development facilities
will be authorized. The ROP further
specifies that the design and location of
facilities must be such that disturbance
to yellow-billed loons is minimized.
Based on the best scientific and
commercial information currently
available, the BLM agrees with the
Service that this objective can best be
achieved by prohibiting development
within 1.6 km (1 mi) of detected nests
and 500 m (1,640 ft) around the
shorelines of lakes 10.1 ha (25 ac) or
larger (Galterio, in litt. 2008).
According to the BLM (Galterio, in
litt. 2008), to account for new
information that might be obtained in
the future (such as information about
yellow-billed loons, specific
development proposals, and their
potential impact on yellow-billed
loons), both the Northwest and
Northeast Records of Decision would
allow for exceptions or deviations from
enumerated buffers in limited
circumstances. In these circumstances,
the exception or deviation would still be
required to meet the management
objective of minimizing disturbance to
the species and would, at a minimum,
need to provide the same level of
protection that the existing buffers
provide. The evaluation of a deviation
request that could affect yellow-billed
loons would be made with close
collaboration and extensive discussions
with subject-matter experts at the
Service and academia to ensure the
conservation of the species.
Although data are not available to
determine how effective the stipulations
and ROPs will be in minimizing or
eliminating adverse impacts to the
species, BLM has expressed a
commitment to measures aimed at
minimizing potential impacts to yellowbilled loons from activities within the
purview of BLM’s authority as a land
management agency (V. Galterio, in litt.
2008). We believe that BLM’s
stipulations and ROPS will likely be
adequate to mitigate potential impacts
to the yellow-billed loon in Alaska, if
careful monitoring and coordination
with the Service continues.
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The Service, National Park Service,
Alaska Department of Natural
Resources, ADFG, and the North Slope
Borough entered into a ‘‘Conservation
Agreement for the Yellow-billed Loon
(Gavia adamsii)’’ (Conservation
Agreement 2006, pp. 1–29) in November
2006. The agreement specifies the goal
of protecting the yellow-billed loon and
its habitat in Alaska and identifies
several strategies for achieving this goal.
These strategies include implementing
actions to reduce the impacts of oil and
gas activities; determining and reducing,
if necessary, impacts from subsistence
activities; and inventorying, monitoring,
and conducting research on the yellowbilled loon. While the agreement
demonstrates the parties’ good-faith
efforts to identify and undertake
protective measures for the loon and its
habitat, it does not require any specific
actions to be undertaken to achieve its
goals or specify any time frames for
doing so, nor does it establish any
quantifiable, scientifically valid
parameters by which to measure
achievement of the objectives and gauge
progress. Thus, we are unable to
conclude with sufficient certainty that
the agreement is likely to be effective in
protecting the yellow-billed loon; so we
did not rely on it for our analysis in this
finding. This is consistent with the
Service’s 2003 ‘‘Policy for Evaluation of
Conservation Efforts When Making
Listing Decisions’’ (PECE) policy, which
sets forth criteria to be used to
determine whether conservation efforts
that have yet to be implemented or
show effectiveness contribute to making
listing a species as threatened or
endangered unnecessary.
In summary, Russia is the only nation
that includes the yellow-billed loon on
an endangered or sensitive species list.
Some countries (Canada, Japan, Norway,
Russia, and the United States) have laws
that prohibit the hunting of migratory
birds such as the yellow-billed loon,
unless specific regulations are issued, or
unless the animals are harvested for
subsistence. Provisions to prevent
habitat degradation for wildlife and
migratory birds or to protect the
environment exist, but enforcement
levels are unknown and in some
countries may not be effective at
protecting habitats. In the United States,
the MBTA prohibits killing of yellowbilled loons, but does not provide for
habitat protection. The Bureau of Land
Management, the land management
agency with authority over most of the
yellow-billed loon’s breeding range in
Alaska, has instituted protective
measures for the species and its habitat.
However, existing regulatory
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mechanisms have not been adequate to
eliminate all threats to the yellow-billed
loon throughout its range. In particular,
despite the fact that the species is closed
to subsistence hunting in Alaska,
harvest surveys have recorded a
substantial level of harvest. We believe
that future take at a level consistent
with these prior levels would cause a
population-level decline that constitutes
a threat to the species (see Factor E,
below). Therefore, we conclude that
existing regulatory mechanisms are
inadequate to protect the species.
Factor E: Other Natural or Man-Made
Factors Affecting its Continued
Existence
Direct Effects of Oil and Gas
Development and Vessel Traffic
Yellow-billed loons spend the
majority of their life in the marine
environment, and are exposed to
potential impacts of disturbance,
collisions with oil and gas structures,
and spills of oil and toxic substances
from offshore oil and gas development
and other vessel traffic. Offshore oil and
gas development might also affect
terrestrial yellow billed loon habitats
(e.g., through construction of pipelines,
support facilities, etc.). Those impacts
are discussed under Factor A.
The magnitude of potential impacts
from offshore oil and gas development
is related to the type, size, and
probability of development, and its
location in relation to yellow-billed loon
distribution and use of an area. Yellowbilled loons are widely dispersed during
most of their annual cycle, so the largest
potential for impacts to a number of
individuals from a single environmental
perturbation is in spring, when
localized, temporary concentrations
occur in migration. Adult loons gather
in polynyas and ice leads and along
open shorelines near river deltas on the
coasts of northern Alaska and Canada. It
is likely that there are similar
movements and concentrations of
yellow-billed loons near Russian
breeding areas in spring, but we have
not found documentation of such
activity. The oil industry is active in
these areas, as demonstrated by existing
projects such as Pioneer’s Ooogrurk
field, BP Alaska’s Northstar
development, and exploration activities
in the Chukchi and Beaufort Seas by
Shell Inc., ConocoPhillips, and others.
In Alaska, exploration and production
are active in Federal and State lease
tracts in the Chukchi and Beaufort Seas
where loons gather in spring and
summer offshore from yellow-billed
loon breeding areas on the ACP
(USMMS 2008, p. 1; ADNR 2008, p. 1).
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In Canada, offshore resources are being
explored and developed in the southern
Beaufort Sea near the McKenzie Delta,
where loons gather in polynyas and ice
leads in spring to stage before arriving
on breeding grounds (Canada Indian
and Northern Affairs 2008, p. 1).
Offshore drilling and ship traffic occur
in the area of the Amundsen Gulf and
Cape Bathurst Polynya, where yellowbilled loons are common in spring
(Mallory and Fontaine 2004, p. 52).
Development could also continue north
of yellow-billed loon breeding areas in
the arctic Islands, where the Sverdrup
Basin contains oil and gas reserves. In
western Russia, offshore projects at the
western edge of yellow-billed loon
breeding grounds in the Barents Sea
include the Shtokman gas field
currently in planning stages. Gazprom is
developing offshore gas fields in the
Kara Sea near the Yamal Peninsula.
Undiscovered reserves are thought to
occur in the East Siberian Sea and the
Laptev Sea Shelf in the Arctic Ocean,
but exploration has not occurred there
(EIA 2008, p. 1; USGS 2007, pp. 1–2).
Oil and gas development are ongoing
in migration and wintering areas. An
offshore lease sale is planned for Bristol
Bay near the wintering location of a
yellow-billed loon tagged with a
transmitter on Seward Peninsula
breeding grounds (U.S. Minerals
Management Service 2008, p. 1). In
Russia, reserves of oil and gas in the Sea
of Okhotsk are large, and just beginning
to be exploited. Drilling is planned off
the west coast of Kamchatka (Rosneft
2008, p. 1), where tagged yellow-billed
loons have passed in migration and
wintered. Development around Sakhalin
Island in the southern Sea of Okhotsk
includes three offshore fields under the
Sakhalin I project and two fields under
Sakhalin II. Sakhalin II is ‘‘the world’s
largest integrated, export-oriented oil
and gas project,’’ including an oil
terminal and Russia’s first liquefiednatural-gas plant at Aniva Bay (Royal
Dutch Shell 2008, p. 1) where tagged
yellow-billed loons have passed in
migration and wintered. Exploration
continues for additional Sakhalin fields.
Norway is among the 10 largest
producers of oil and gas in the world,
with all its production offshore in the
North, Norwegian, and Barents Seas
(Norwegian Petroleum Directorate 2008,
p. 1–1, Figures 3.2–3.5). Production of
oil is expected to decline slowly, while
gas production will increase, depending
on future discoveries (Norwegian
Petroleum Directorate, p. 1–3). Seismic
studies are occurring in the Lofoten
fishing grounds currently closed to oil
and gas development under a regional
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management plan (Royal Norwegian
Ministry of the Environment 2006, pp.
1–144); this area is offshore from the
largest concentrations of yellow-billed
loons wintering along the Norwegian
coast (Strann and Ostnes 2007, Figure
2). The management plan will be
updated in 2010, with an opportunity to
open the area to drilling.
Air and boat traffic associated with oil
and gas development could disturb
yellow-billed loons, decreasing foraging
success or displacing individuals to less
preferred areas at some unknown
energetic costs. The severity of
disturbance and displacement effects
depends upon the duration, frequency,
and timing of the disturbing activity.
Hence, construction and operation of
offshore facilities, which could persist
for years, will likely have greater
impacts than seismic and exploratory
activities, which generally last less than
one year. Depending upon the frequency
of operations and routes traversed by
vessels and aircraft, impacts could range
from negligible (few yellow-billed loons
encountered at irregular intervals) to
substantial (vessels or aircraft
repeatedly encounter yellow-billed
loons). Expected increases in arctic
shipping traffic due to reduced summer
sea ice are discussed in the Climate
Change section under Factor A.
Offshore oil and gas development
would result in both fixed (e.g., offshore
platforms) and mobile structures (e.g.,
supply ships) in the marine
environment, posing a potential
collision risk for yellow-billed loons.
Birds are particularly at risk of collision
with objects in their path when
visibility is impaired during darkness or
inclement weather, such as rain, drizzle,
or fog (Weir 1976, p. 6). In a study of
avian interactions with offshore oil
platforms in the Gulf of Mexico, Russell
(2005, pp. 266–297) found that collision
events were more common and more
severe (by number of birds) during poor
weather. Weather conditions that
increase collision risk are common in
northern waters such as the Bering,
Beaufort, and Chukchi Seas. Without
knowing the number, location, and
design of structures that would result
from offshore oil and gas development,
it is difficult to estimate the number of
yellow-billed loons that would pass by
structures during migration.
Vulnerability to collision with
structures probably varies among
species, but we are not aware of
information on the propensity of
yellow-billed or other loons to collide
with structures.
Spills of oil, refined petroleum
products (e.g., diesel fuel), or other toxic
substances (e.g., drilling mud) from
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offshore oil and gas development can
occur as a result of well blowouts,
operational discharges, pipeline
failures, tanker or other vessel leaks,
and numerous other potential accidental
discharges (AMAP 2007, pp. 24–25). A
discharge of these products could cause
direct mortality of yellow-billed loons
or result in indirect effects through
habitat degradation or killing prey
species.
Mortality following exposure to oil is
common in aquatic birds, which are
vulnerable to surface oil (Albers 2003,
pp. 354–356). External oiling disrupts
feather structure, causes matting of
feathers, and permits wetting of the
bird, and death typically results from
hypothermia and drowning (Vermeer
and Vermeer 1975, pp. 281–295; Jenssen
1994, pp. 207). Ingesting petroleum
through feather preening or
consumption of contaminated food or
water, and inhalation of fumes from
evaporating oil, might not be
immediately lethal, but debilitating
effects include gastrointestinal
irritation, pneumonia, dehydration, red
blood cell damage, impaired
osmoregulation, immune system
suppression, hormonal imbalance,
inhibited reproduction, retarded growth,
and abnormal parental behavior
(Jenssen 1994, pp. 207–211; Hartung
and Hunt 1966, pp. 564–569; Miller et
al. 1978, pp. 315–317; Szaro et al. 1981,
pp. 791–798; Leighton 1993, pp. 93–99;
Fry et al. 1986, pp. 455–462; Eppley
1992, pp. 309–311; Fowler et al. 1995,
pp. 383–387; Walton 1997, pp. 264–267;
and Briggs et al. 1997, pp. 718–723).
These effects can cause death from
starvation, disease, or predation,
especially in the harsh arctic
environment.
In northern seas it is difficult to
contain and clean up spilled petroleum
products due to ice, high winds, and
high seas. A spill can result in persistent
environmental contamination by oil and
its toxic breakdown products and
reduced food resources, resulting in
lower survival and hydrocarbon
exposure years after visible oil has been
abated (Esler et al. 2000, p. 843; Trust
et al. 2000, pp. 399–402).
While a large spill in an area
supporting large numbers of yellowbilled loons could have significant
adverse effects, we consider the relative
probability of such an event to be very
low. First, the likelihood of
development occurring in areas where
loons gather is low. For example, the
U.S. Minerals Management Service
calculates the probability of commercial
success resulting from their lease sale
193 in the Chukchi Sea to be 10 percent
(USMMS 2006, p. 2). Second, if
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development occurs, spills are relatively
infrequent, even in the arctic. To date,
there have been no large oil spills in the
arctic marine environment from oil and
gas activities (AMAP 2007, p. 24). No
exploratory drilling blowouts have
occurred from the 98 wells drilled to
date in Alaska’s arctic offshore region
(USMMS 2007, Appendix A.1, p. 2). In
fact, of the 13,463 exploratory wells that
have been drilled in the coastal United
States, there were 66 blowouts during
drilling, only 4 of which resulted in oil
spills (range 1 to 200 bbl; average 78 ∼
bbl) (USMMS 2007, Appendix A.1, p.
2). Finally, even if a spill occurred, the
chances that it would occur close to
loons in the seasonal window of time
when they are present is also small.
Oil and gas exploration, production,
and transportation, as well as spills
from other vessel traffic, could also
affect migrating and wintering yellowbilled loons, as described below, but we
believe this risk factor is minimized
because yellow-billed loons are widely
distributed and, therefore, at extremely
low densities throughout most of the
year when they are at sea. The 1989
Exxon Valdez tanker spill killed an
estimated 17 to 50 yellow-billed loons
in Prince William Sound, Alaska (Earnst
2004a, p. 21). There is oil and gas
development in the Sea of Okhotsk,
including on and around Sakhalin
Island and off the west coast of
Kamchatka. Oil and gas development
also occurs in yellow-billed loon
wintering areas in Norwegian waters,
and oil spills at drilling sites and due to
vessel accidents occur. Due to the
importance of the Norwegian fishing
industry, regulation of offshore oil
development has been protective.
However, it is possible that in 2010
Norway will allow oil development in
the Lofoten fishing grounds offshore
from a yellow-billed loon wintering
area. The Sea of Japan and the Yellow
Sea, bordering China, North and South
Korea, and Japan, have high levels of
vessel traffic subject to oil spill
accidents, with several ports among the
world’s top 25 in cargo transported. In
December 2007, the crude oil carrier MT
Hebei Spirit caused South Korea’s worst
oil spill to date, estimated at 71,000 bbl
in the Yellow Sea near where yellowbilled loons tagged with transmitters
have been located in winter. In
December 2004, the freighter M/V
Selendang Ayu grounded and broke in
half in the Aleutian Islands of Alaska,
spilling more than 8,000 bbl of oil. One
yellow-billed loon was observed to be
oiled in the vicinity of the spill (Byrd
and Daniel 2008, p. 6). Yellow-billed
loons wintering in marine waters off
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southern Alaska, British Columbia, and
around Great Britain could also
encounter spills, primarily from vessel
traffic.
Yellow-billed loons face the
possibility of oil spills throughout their
range. The one breeding population for
which we have population trend data,
the ACP population, is stable or slightly
declining at present. We would expect
a steep decline if cumulative oil spills
were affecting this population, which
winters in Asian waters. We do not have
evidence that marine oil spills are
causing population-level effects to
yellow-billed loons on the ACP. The
Asian wintering grounds are likely to
harbor the most oil spills due to vessel
accidents compared to other wintering
areas, so it is reasonably likely that
breeding populations that winter
elsewhere are not at greater risk than the
birds that winter in Asia.
In summary, at present we believe the
risk to yellow-billed loons from offshore
oil and gas development and shipping
traffic accidents to be low. Moreover,
the one breeding population for which
we have population trends does not
appear to be declining steeply due to
this risk factor. Although the amount of
oil and gas development and shipping
traffic will likely increase in the future,
the associated risk is reasonably likely
to be partly or wholly offset by
improved technologies and regulation,
such as the U.S. Oil Pollution Act of
1990. Also, the species’ wide
distribution and extremely low densities
throughout most of the year when birds
are at sea reduces the risk of populationlevel impacts from any single event. As
offshore oil and gas development and
shipping traffic continue, individual
yellow-billed loons will likely continue
to be negatively affected as a result of
collisions with vessels or structures and
oil spills. However, we cannot reliably
predict that the species will be affected
at the population level, given the
considerable uncertainty of the location
of such events and the effectiveness of
the design and operational spill cleanup
methods that may be employed.
Therefore, we find that oil and gas
development and vessel traffic is not a
threat to the yellow-billed loon now or
in the foreseeable future.
Subsistence Harvest
Subsistence harvest of yellow-billed
loons in the Bering Strait has been
reported at levels that we expect would
cause impacts to the species in the
foreseeable future. Although we have
concerns about the degree of accuracy of
the reported numbers of yellow-billed
loons harvested, as discussed below, we
believe that the likely magnitude of
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actual harvest levels constitutes a threat
to the species rangewide.
Subsistence hunting of wild birds,
including loons, is an important
component of the customs, traditions,
and economies of many cultural groups
in the arctic. Subsistence is defined in
U.S. Federal and State law as the
‘‘customary and traditional uses’’ of
wild resources for a variety of purposes,
including food, clothing, fuel,
transportation, construction, art, crafts,
sharing, and customary trade (Wolfe
2000, p. 1). Yellow-billed loons are
generally not a preferred food in some
parts of their arctic range, but their skin
and feathers are used for ceremonial
purposes (Paige et al. 1996, appendices;
Georgette 2000, p. 19; Syreochkovskiy
2008, p. 2), and they are shot for other
reasons, such as for taxidermy, to chase
them from fishing nets, or out of
curiosity (Syreochkovskiy 2008, p. 2).
Discussions between St. Lawrence
Island, Alaska hunters, and Service
biologists confirmed that Bering Strait
hunters target loons for harvest (Ostrand
in litt. 2009, p. 1). A Service biologist
working with hunters on St. Lawrence
Island in the spring rarely observed
hunters with harvested loons in their
possession (Benter in litt. 2008, p. 1),
although he has observed hunters
targeting loons for harvest (Benter pers.
comm. 2009).
Although it is clear that loons are
harvested for subsistence, there are
challenges to assessing the magnitude of
harvest and biases inherent in the
process. Harvest surveys have been
conducted in many arctic communities,
but they have varied in geographic
coverage, methodology and analysis,
and level of detail; thus, comparing
among areas or detecting trends over
time is difficult (SHSAC 2003, p. 5).
Most survey data are collected through
recall interviews conducted a month or
more after harvest, resulting in varying
and unknown levels of recall error.
Sampling designs might inadequately
survey rarely taken species (SHSAC
2003, p. 15), and there have been no
surveys specifically targeting yellowbilled loons. As a result, most yellowbilled loon harvest estimates have a
high level of variance and yield results
of unknown accuracy. In some surveys,
loons are not identified to species; in
others misidentification of species
harvested probably occurs but to an
unknown degree. To consider
misidentification issues, we present
some data below on other loon species
reported in harvest surveys.
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I. Alaska
Surveys Conducted Prior to Migratory
Bird Subsistence-Harvest Regulations
As stated in Factor D, yellow-billed
loons are not open for subsistence
hunting in Alaska under migratory bird
subsistence-harvest regulations. Prior to
the establishment of Federal regulations
authorizing subsistence harvest for
migratory bird species in 2003,
subsistence harvest surveys for
migratory birds were conducted
sporadically, and coverage varied
considerably among surveys.
Yellow-billed loons migrate through
the Chukchi and Bering Sea, making
them available for harvest during spring
and fall migration in northwest Alaska.
In the Northwest Arctic Borough (the
area around Kotzebue, Alaska) harvest
surveys (from 1994–1998; Georgette
2000, pp. 1–218), no yellow-billed loons
were reported, but 71 common, 2 arctic,
6 red-throated, and 1 unknown loon
were reported, with identification of
species noted as uncertain at times
(Georgette 2000, p. 10). Loons
comprised generally less than one
percent of the total bird harvest
(Georgette 2000, p. 19). A one-year
survey of the two villages on St.
Lawrence Island in the Bering Strait
from 1995–1996 reported 40 yellowbilled loons and 290 common, 81
Pacific, and 15 unknown loons
harvested (ADFG and Kawerak 1997, p.
2). Concerns about misidentification of
species, particularly identification of
common loons, which are rare in the
Bering Strait, are discussed below.
Yellow-billed loons migrate along the
coast of the Yukon/Kuskokwim Delta
and Bristol Bay regions, so harvest in
spring and fall is possible. Because
yellow-billed loons do not breed in
these regions, reports of summer and
egg harvest suggest misidentification.
Below we report the long-term harvest
survey record for these areas. Because
reports give summary results
overlapping the pre- and post-2003
regulation period, we report the entire
survey record here, including post-2003
results.
Yellow-billed loons have been
reported in almost every annual YukonKuskokwim Delta harvest survey
(conducted 1985 to present, except
2003, with methodology changes in
2001 and 2002; Wentworth 2007b, p.
12). The 2001–2006 5-year average
yellow-billed loon harvest was 44 ± 78
SD (standard deviation, a measure of the
dispersion of the data around the mean)
(range 0–183) for the Yukon/
Kuskokwim Delta (calculated from
Wentworth 2007b, p. 36 and USFWS et
al. 2008, Table 2006–17a). Yellow-billed
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loon eggs were reported taken in 14 of
20 years, with an annual average of 14
eggs per year estimated for 2001 through
2005 (Wentworth 2007b, pp. 37–41).
Yellow-billed loons have been
reportedly taken in every Bristol Bay
region survey (since 1995, except no
surveys in 2000 and 2003, surveys were
limited to Togiak NWR in 1996, 1998,
and 2006, and methodology changed in
2001 and 2002; Wentworth 2007a, pp.
1–2). The 2001–2005 Bristol Bay region
average yellow-billed loon harvest was
78 ± 128 SD (range 5–269) (Wentworth
2007a, p. 22). From 1995–2005, the only
eggs reported in Bristol Bay were in
1997, when 27 eggs were estimated
taken (Wentworth 2007a, pp. 23–24).
Harvest Surveys Conducted Subsequent
to Migratory Bird Subsistence-Harvest
Regulations
In 2004, a new Alaska-wide
subsistence-harvest survey, including
spring, summer, and fall seasons, was
initiated subsequent to the 2003
implementation of migratory bird
subsistence-harvest regulations. Under
the new regulations, areas of Alaska
eligible for migratory bird subsistenceharvest are divided into regions that are
surveyed periodically (map available at
https://alaska.fws.gov/ambcc/
Regulations.htm). The new survey has
yet to be conducted simultaneously
within a year in all villages or all
regions (USFWS et al. 2008, p. 3), and
the 2004–2006 summary report states
that the results should be used with
caution due to possible inaccuracies,
unreliable data, and insufficient sample
size (USFWS et al. 2008, p. 3). Within
the area covered by the new survey,
yellow-billed loons are most likely to
occur in the North Slope, Northwest
Arctic, and Bering Strait/Norton Sound
regions during nesting and in Bristol
Bay and Yukon/Kuskokwim regions
during migration; they were reported as
harvested in the Bering Strait/Norton
Sound, Bristol Bay, North Slope, and
Yukon/Kuskokwim Delta regions in
2004–2006 (Table 1). The largest
number of yellow-billed loons and other
loon species were estimated for the
Bering Strait/Norton Sound region
(Table 2).
TABLE 1—ESTIMATED HARVEST OF YELLOW-BILLED LOONS (EXCLUDING EGGS) IN ALASKA REGIONS REPORTING TAKE OF
THE SPECIES IN THE YEARS 2004–2006. NO OTHER REGIONS REPORTED YELLOW-BILL LOON TAKE. DATA EXTRACTED FROM TABLES IN USFWS ET AL. 2008
Year
2004
Region
Estimated
harvest
Bering Strait ...............................
2005
2006
Total
95% CI
Seasona
Estimated
harvest
95% CI
Season
Estimated
harvest
317 ..........
271–530
45 ............
45–123
Spring ..............
Summer
NSb ..........
362
Bristol Bay .................................
YKD ...........................................
10 ............
4 ...............
8–30 .....
3–16 .....
Spring ..............
Summer
Fall
Fall
Spring ..............
5 ...............
12 ............
2–22 .....
(c) .........
0 ...............
0 ...............
15
16
North Slope ................................
NS ............
..............
..........................
3 ..............
2–14 .....
Spring ..............
Spring ..............
Summer
Fall
Summer ...........
NS ...........
3
0 ...............
396
Total ....................................
331
65
CI = confidence interval
a Seasons that yellow-billed loons were reported as harvested.
b NS = region not surveyed in that year.
c For Yukon/Kuskokwim Delta (YKD) in 2005, 11 yellow-billed loons reported in the Kuskokwim River subregion (95 percent CI 8–53) and one
reported in North Coast subregion (95 percent CI 1–23).
TABLE 2—ESTIMATED HARVEST OF LOONS FOR THE BERING STRAIT/NORTON SOUND REGION IN 2004 AND 2005. DATA
EXTRACTED FROM TABLES IN USFWS ET AL. 2008
Year
Species
2004
Number
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Yellow-billed loon .............................................................................................................................
Common loon ..................................................................................................................................
Pacific loon ......................................................................................................................................
Red-throated loon ............................................................................................................................
We recently received preliminary
subsistence-harvest estimates for 2007
(Naves 2008, pp. 1–30). For 2007, Naves
(2008, pp. 1–31) reported results by
subregion rather than by region as
reported previously; thus these
observations are not directly comparable
to data in Tables 1 and 2 and are not
included therein. Naves (2008, p. 7)
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01:29 Mar 25, 2009
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reported that an estimated 1,077 (95
percent CI = 808–1,347) yellow-billed
loons and 2,492 (95 percent CI = 2,158–
2,826) common loons were harvested for
a Bering Strait/Norton Sound subregion
that includes two villages on St.
Lawrence Island and one on Little
Diomede Island, called the St.
Lawrence-Diomede Islands subregion
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317
405
498
26
2005
95% CI
271–530
345–889
425–772
22–89
Number
45
891
33
15
95% CI
45–123
871–1438
18–115
10–82
(SL-DI subregion). This estimated SL-DI
subregion yellow-billed loon harvest
was allocated among seasons with 5
birds estimated harvested in spring, 362
in the summer, and 711 in the fall.
Estimated harvest of common loons in
the SL-DI subregion were 166 in spring,
560 in summer, and 1,766 in fall (Naves
2008, p. 7). Harvest of 76 Pacific loons
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(95 percent CI = 19–134) and 366 redthroated loons (95 percent CI = 221–
511) was also estimated for the
subregion (Naves 2008, p. 7). Yellowbilled loons were not reported for any
other subregion in the Bering Strait/
Norton Sound Region. The Barrow
subregion of the North Slope region was
the only other surveyed area that
reported harvest of yellow-billed loons
in 2007, with an estimated 84 (95
percent CI = 32–135) yellow-billed
loons harvested (Naves 2008, p. 15).
Interpretation of the 2007 loon harvest
estimates requires consideration of
several factors (beyond their magnitude
and potential population-level impact,
which will be discussed later). First, the
confidence intervals (which are
mathematical estimates of the reliability
of the estimate, and in this case are
expressed as a percent of the estimated
value) surrounding the estimates of both
yellow-billed and common loons are
comparatively small. The 2007 survey
results for the SL–DI subregion have a
95 percent CI that is only 25 percent of
the estimate for yellow-billed loons and
13 percent for common loons (Naves
2008, p. 7); these are much smaller than
earlier estimates given for the entire
Bering Strait/Norton Sound region (for
example, the 2005 95 percent CI was
174.2 percent of the estimate for yellowbilled loons and 61.4 percent for
common loons (USFWS et al. 2008,
Table 2005–2a)). These smaller CI
values indicate increased precision in
the 2007 subregional estimate compared
to the earlier regional estimates, which
reflects large sample size (82 of 318
households (26 percent) sampled) and
low variation among households
(indicating that most households
reported taking fairly comparable
numbers of loons).
A second consideration in
interpreting the large estimate of yellowbilled loon harvest for 2007 is possible
misidentification. Large numbers of
common loons are reported as harvested
in the SL/DI subregion where they are
a rare to uncommon visitor (Fay and
Cade 1959, p. 100; Kessel 1989, p. 66;
North 1994, p. 3; Armstrong 1995, p. 23;
McIntyre and Barr 1997, p. 2; Lehman
2005, p. 15). The report described above
of 290 common loons taken on St.
Lawrence Island in 1995–1996 (ADFG
and Kawerak 1997, p. 2) is considered
by Lehman (2005, p. 15) to result from
misidentification because only two
verified records of this species from the
island are known to date. Similarly,
common loons reported as harvested
from the Bering Strait/Norton Sound
region in 2004 and 2005 (Table 2) likely
also include other loon species, possibly
including yellow-billed loons.
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A potential source of
misidentification is the probable
presence in the fall of juvenile loons
whose plumage resembles adult basic
(i.e., non-breeding or winter) plumage. It
is difficult to differentiate among loon
species in this plumage, and survey
forms do not illustrate this plumage or
highlight ways to distinguish among
species. It is unknown how many
common loons move through the Bering
Strait, but as described above, the
number is thought to be small since they
have rarely been seen on St. Lawrence
Island. Therefore, if misidentification is
attributable to confusion between
yellow-billed and common loons, the
actual harvest of yellow-billed loons is
likely even greater than that reported. It
is also possible that Pacific and redthroated loons are misidentified as
yellow-billed and common loons,
although they are notably smaller. If so,
this would result in actual harvest of
yellow-billed loons being less than that
reported.
We considered the possibility that a
large number of households in the
subregion misidentified loons due to
survey deficiencies, and we considered
the possibility that this problem was
worse in 2007 than in earlier years,
resulting in a higher estimated harvest
than in previous years. The survey
forms show color pictures of birds
exclusively in breeding plumage, and
survey respondents are asked to mark
the number taken next to the pictures.
The lack of depictions of winter and
immature plumages in the survey form
is a likely problem for harvest reported
in the fall, when immature birds are
likely to be harvested. There is no need
for the respondent to identify the name
of the bird, making it less likely that
cultural differences in nomenclature
would cause systemic misidentification.
The surveyors were trained in a
standard manner for all surveys across
the state in all years, using a manual
developed over many years. In the
Bering Strait/Norton Sound region, the
surveyors were provided with several
bird identification books to assist them,
although it is unknown how and how
often they used the books during
surveys (Ostrand in litt. 2009, p. 1). In
summary, we found that
misidentification could be occurring
because the survey form includes only
breeding plumages. We found no reason
to conclude that the survey was
conducted any differently in 2007 than
in previous years.
Above we noted the large inter-annual
variation in harvest estimates of yellowbilled loons for the Bering Strait/Norton
Sound region (Table 2); this variation is
increased with the addition of the large
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estimated harvest in the 2007 survey
(Naves 2008, p. 7). Large inter-annual
variation in estimated harvest of yellowbilled loons could represent
measurement error for a relatively
constant rate of harvest, or it could
represent actual variation in harvest
among years. Schmutz (in litt. 2008, p.
1) observed that some yellow-billed
loons fitted with transmitters in 2002,
2003, and 2007 on Alaskan breeding
grounds moved to marine waters near
St. Lawrence Island before migrating
south, but others, including all eight
birds fitted with transmitters in 2008,
moved from Alaskan breeding grounds
to Kolyuchin Bay on the north side of
the Chukotka Peninsula, and crossed
overland to the southwest over the
peninsula and into Anadyr Bay, thereby
avoiding the St. Lawrence Island area.
Thus, migratory behavior may vary from
year to year based on some unknown
environmental factor, and loon harvest
could vary with changes in the number
of loons moving past hunting areas in
different years.
Because the 2007 estimated harvest
was substantially higher than earlier
estimates, we evaluated issues specific
to the 2007 survey that might help
explain this difference. Other than the
fact that the survey for all three seasons
was conducted at the end of the fall
season, survey protocols were followed,
and no other factors were identified to
explain the high estimate (Ostrand in
litt. 2009, p. 1). Conducting the survey
at the end of the year means that the
respondents would have to recall what
they harvested months earlier, which
could reduce the accuracy of the survey,
especially for the earlier seasons.
Although we examined potential
flaws in the harvest survey data and
concluded that some birds could have
been misidentified, we believe the data
are reliable enough to identify the order
of magnitude of likely harvest. We
conclude that on average, hundreds of
yellow-billed loons are probably taken
annually in the Bering Strait region. In
addition, tens are likely taken in other
parts of Alaska, particularly the North
Slope.
To evaluate the effect of this harvest
on the yellow-billed loon, we examined
what we know about the number of
birds that move through the Bering
Strait. As described in the Species
Biology section, above, all 29 marked
Alaskan breeding birds used the Bering
Strait or Chukotka Peninsula during
migration. There are an estimated 3,000
to 4,000 Alaskan breeding birds. It is
likely that, due to their proximity, 3,000
to 5,000 eastern Siberian breeding
yellow-billed loons also migrate through
the Bering Strait region. Observations of
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yellow-billed loons during migration on
the Beaufort Sea provide evidence that
at least some Canadian breeding birds
use this migration route, most likely the
3,750 to 6,000 breeding birds estimated
to occur on Banks and Victoria Islands
and the adjacent arctic mainland coast.
Thus, we believe it is likely that a large
part of the rangewide population moves
through the Strait and is subject to
harvest there. We do not know whether
the actual rangewide breeding
population is closer to 16,000 or 32,000,
but as discussed in the Population Size
section, we believe it is likely closer to
16,000.
We next evaluated whether hundreds
of yellow-billed loons being harvested
annually would be unsustainable to the
rangewide population. We examined a
population model developed by the U.S.
Geological Survey (USGS) to test the
sensitivity or response of the population
to a range of possible harvest levels
(Table 3; Schmutz 2009, p. 15). The
model was constructed to begin with
stable populations (i.e., lambda = 1.00),
and then examined whether harvest
caused additional declines. The model
considered a range in harvest mortality
rates and population sizes to reflect our
uncertainty about these parameters. We
believe the model includes the entire
range of possible values for the size of
the affected population.
The model suggests that for all
scenarios, harvest would cause an
otherwise stable population to decline
(i.e., lambda declines from 1.00 to
values below 1.00) (Table 3). The annual
average values for harvest that we
believe are most likely (i.e., hundreds;
best approximated in Table 3 by the
column corresponding to a harvest of
317 birds) and the population size we
believe is subjected to the harvest (i.e.,
approximately 16,000 plus 1 and 2 year
old birds; best approximated in Table 3
by the row corresponding to a
population size of 18,764, which
includes 1 and 2 year olds) show that a
hypothetical stable population that
experienced added harvest of 317 birds
would decline by half in 41 years, or
less if the harvest is larger or varies
among harvest estimates for recent years
(Table 3). Even if there are 37,528
yellow-billed loons in the rangewide
population subject to harvest (which we
think is unlikely, as discussed above), a
harvest of 317 birds would cause the
population to decline by half in 83
years. We believe this harvest and
associated declines would be
unsustainable to the rangewide
population, causing a long-term
decrease in abundance that would be
difficult to reverse due to the low
reproductive potential of the species. It
is important to note that this analysis
does not take into account that
additional mortality, such as harvest in
other parts of Alaska, Russia, or Canada,
or from other sources, could exacerbate
the rate of decline from a stable
population.
Table 3. Model results of the effects of
various harvest scenarios on trend and
population size of yellow-billed loons.
The starting model predicted a stable
population (trend = 1.0). This model
used productivity data from yellowbilled loons on the Colville Delta, and
survival rates allocated among age
classes similar to Mitro et al. (2008) for
common loons, but with an adjustment
factor to achieve hypothetical
population stability so that the model
could evaluate likely population
response to varying levels of harvest.
Thus, the starting, stable population
shown in the first column represents a
population without harvest. Reference
population sizes used breeding
population sizes of 4,000, 10,000,
16,000 and 32,000 breeding birds, and
were then adjusted to include an
additional population component
comprised of individuals (likely 1- and
2-year olds) that remain at sea and are
not counted during summer surveys of
tundra habitats. The next three data
columns represent three starting levels
of harvest corresponding to recent
harvest estimates for the Bering Straits
region. The fourth data column
represents population response to
harvest levels that vary among years,
which reflects reported variation in
harvest and satellite tracking data that
indicate inter-annual variation in
migratory behavior through the Bering
Strait. For all harvest levels, the
mortality rate, rather than mortality
number, from harvest is kept constant
across the years of each population
projection. In each cell, there are two
numbers. The first is annual population
growth rate, given the indicated harvest
and the population that such harvest is
allocated to. Second is the number of
years from present until the population
falls below half of current size. These
harvest estimates and corresponding
predicted population responses do not
consider possible additional harvest
occurring outside of the Bering Straits
region in other portions of the species’
life cycle. This model assumes hunting
mortality is additive and not
compensatory. From Schmutz 2009, p.
15.
Beginning harvest level to set mortality rate
45
317
1,077
N = 4,508 ...................................................................................................................
0.9900
70
0.9297
10
0.7611
3
0.8937
6
N = 10,372 .................................................................................................................
0.9957
162
0.9695
23
0.8962
7
0.9538
15
N = 18,764 .................................................................................................................
0.9976
295
0.9832
41
0.9426
12
0.9745
27
N = 37,528 .................................................................................................................
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Reference population ................................................................................................
0.9988
601
0.9916
83
0.9713
24
0.9873
54
In summary, although there is
uncertainty about the reported numbers
of yellow-billed loons harvested in
Alaska, these surveys represent the best
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information available to us at this time.
We believe that the data are reliable
enough to conclude it is likely that
recent annual average harvest of yellow-
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Annually rotate
between 45,
317, and
1,077
billed loons in Alaska is in the
hundreds. Based on this information,
the large number of yellow-billed loons
from Alaskan, Russian, and Canadian
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breeding areas that are likely to use the
Bering Strait in migration, and the
model results presented in Table 3, we
conclude that the potential impact of
the Alaska harvest on the rangewide
yellow-billed loon population is
significant. It is possible that recent high
harvest estimates represent a new
phenomenon not yet reflected in
population trend information, although
we do not have information on whether
the harvest will increase or decrease in
the future. Harvest at the present
magnitude, even if occurring every few
years, will cause a rangewide decline
that constitutes a threat to the yellowbilled loon.
II. Russia
The Red Data Book of the Russian
Federation (2001, p. 367) states ‘‘during
the nesting period, loons are often
killed/harvested by the indigenous
population for food and pelts
particularly in the northeast of Russia.’’
Other information comes from a recent
review from the Russian Academy of
Sciences to the Service, which reported
current yellow-billed loon harvest of
approximately 200 per year, including
for protection of fishing nets
(Syroechkovskiy 2008, p. 1–2). The
review also noted that in former times
yellow-billed loons were occasionally
shot by indigenous peoples for ritual
purposes and raw materials, and
conversely, some tribes in the Yakutian
arctic recognize loons as sacred species
and never shoot them (Syroechkovskiy
2008, p. 1).
The basis for the Russian estimate of
yellow-billed loon harvest above is
unknown. Few surveys have been
conducted (limited information from
Yakutia and Chukotka), the species’
range has not been adequately sampled,
and the species has an uneven
distribution across Russia
(Syroechkovskiy 2008, p. 1). No
subsistence harvest information is
available from the Taymyr Peninsula,
one of the two core areas of the breeding
range in arctic Russia and the only
region where Syroechkovskiy (2008, p.
1–2) reported hunting of the species as
a food source.
Other harvest surveys have occurred
in Russia, however. Unidentified loons
were reported taken in two Providensky
communities in 1997 and 1998 as part
of subsistence harvest surveys for
marine mammals (Ainana et al. 1999, p.
83; Ainana et al. 2000, pp. 66 & 71). No
loons were listed in 1999 (Ainana et al.
2001), but this report included fewer
and less detailed reports of birds.
Service-funded waterfowl (eider)
subsistence harvest surveys in 19 of 100
northeastern Russia (Yakutia and
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Chukotka regions) communities within
100 km (62 mi) of the coastline by the
Goose, Swan, and Duck Study Group of
Northern Eurasia from 2002–2005
(Syroechkovski and Klokov 2007, p. 8)
included loons. Yellow-billed loons
reported (by previous year recall of
hunters) varied among villages (range 0–
58), with only three villages reporting
harvesting 10 or more birds. Harvest
was greatest in northern Chukotka,
where the species nests and where one
village reported egg harvest of 44 eggs
in one year. The species’ range was not
completely surveyed because loons
were not the focus of the survey
(Syroechkovski and Klokov 2007, p. 1).
However, based on these surveys, as
well as the nationwide estimate
provided by the Russian Academy of
Sciences (Syroechkovskiy 2008, pp. 2),
we estimate tens to possibly 200 yellowbilled loons are harvested by
subsistence hunters annually in Russia,
virtually all affecting the Russian
breeding population (the breeding
population is estimated to be 5,000 to
8,000). The effect of an annual harvest
of 200 birds on a population of this size
is significant, particularly if the
population is subject to additional
harvest in migration through the Bering
Strait (as described under the Alaska
section above).
III. Canada
Yellow-billed loons are thought to
breed in several of the Native Land
Claims in northern Canada, but
primarily in Inuvialuit and Nunavut.
The land claims are in different phases
of settlement, and harvest data are only
available for those areas where claims
have been settled and Renewable
Resource Boards (RRBs) are in operation
to jointly manage wildlife resources
(https://www.mb.ec.gc.ca/nature/ecb/
da02s11.en.html, accessed October
2008). The RRBs all use similar
methodology to determine wildlife
harvest levels for their areas of
jurisdiction. Reported possible sources
of error in these harvest estimates
include enumeration, coverage and nonresponse, measurement and
questionnaire design, recall failure, and
strategic response bias (Priest and Usher
2004, pp. 35–42).
Harvest survey data are available from
the Nunavut, Inuvialuit, and Sahtu
regions, which encompass the vast
majority of the yellow-billed loon’s
breeding range in Canada (see map at
https://www.mb.ec.gc.ca/nature/ecb/
da02s11.en.html, accessed November
25, 2008), from 1988 to 2003. Nunavut
harvest surveys (Priest and Usher 2004)
were conducted from 1996 through
2001. Five communities reported
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harvesting yellow-billed loons from May
through October, while twenty-two
communities did not report harvest of
yellow-billed (or unidentified) loons.
The estimated yearly harvest (reported
as a range) was 2.6–8.2 yellow-billed
and 1.4–5.8 unidentified loons (Priest
and Usher 2004; tables). Inuvialuit
harvest surveys were conducted from
1988 to 1997 (Inuvialuit Harvest Study
2003). Loons, including yellow-billed
loons, were reported harvested from
May through July in three of six
communities surveyed. Estimated mean
annual harvest of yellow-billed loons for
the region was 10 ± 8 SD, and 1 ± 2 SD
additional unidentified loons per year
(Inuvialuit Harvest Study 2003; tables).
Sahtu Region surveys were conducted
from 1998 to 2003 (Bayha and Snortland
2002, 2003, 2004). (Yellow-billed loons
occur only in the northern Sahtu
region.) No yellow-billed loons were
reported harvested, but a total of 5
unidentified loons were harvested over
the 6 survey years (less than 1 per year)
from May to August (Bayha and
Snortland 2002, 2003, 2004; tables),
with no extrapolation to the entire
Sahtu region. Based on these data, we
estimate low tens of yellow-billed loons
are harvested by subsistence hunters
annually in Canada.
IV. Conclusion for Subsistence
Our ability to accurately estimate the
magnitude of subsistence harvest of
yellow-billed loons rangewide is
compromised by incomplete harvest
survey coverage of the species’ range,
possible misidentification among
species, sampling shortcomings, and our
limited ability to allocate harvest during
migration to source breeding
populations. Correctly assessing
subsistence harvest of a rare species,
such as the yellow-billed loon, requires
intensive surveys to adequately sample
villages within the species’ range to
increase precision in the harvest
estimate. The data do tell us that
yellow-billed loons have been
harvested, probably averaging in the
hundreds annually, which we believe
would be unsustainable relative to the
overall yellow-billed loon population.
Despite the limitations described
above, the best available information
indicates that, throughout its range, on
average, hundreds of yellow-billed
loons from multiple breeding areas are
harvested annually by subsistence
hunters. Population modeling suggests
that the number of yellow-billed loons
being harvested in the Bering Strait area
of Alaska alone is likely unsustainable.
In addition, up to several hundred
yellow-billed loons could be taken
annually on Russian breeding grounds,
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and small amounts of harvest are
reported for other areas in Alaska and
Canada. The lack of precision of the
population trend information for Alaska
could be preventing us from detecting
the impact of this harvest on the
population, or the high harvest
estimates could represent a new
phenomenon not yet manifested in our
population trend estimates. The harvest
is also likely having an impact on
breeding populations that are not being
monitored; population trends for
Canada and Russia are not known. We
have no reason to believe that the
current level of subsistence harvest of
yellow-billed loons will change in the
future. Because we believe that the
rangewide population of yellow-billed
loons is subject to unsustainable levels
of harvest, we find that subsistence
harvest is a threat to the species
rangewide.
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Fishing Bycatch (Commercial and
Noncommercial)
Incidental take (‘‘bycatch’’) from
commercial and subsistence fisheries
poses a risk to yellow-billed loons due
to direct mortality caused by
entanglement or accidental drowning in
gear. Gear type, location, and timing
affect both frequency and intensity of
bycatch rates. Yellow-billed loons are
believed to be attracted to nets by
entangled fish or other loons (J. Bacon
in litt. 2008, p. 1). Yellow-billed loons
spend the majority of the year foraging
in coastal waters; therefore, coastal
fisheries are more likely to encounter
loons than pelagic fisheries. Thus, our
primary concern is assessing the current
level of bycatch occurring in nearshore
gill-net fisheries that overlap the yellowbilled loon’s range. Immature yellowbilled loons (1–2 year olds), which are
thought to remain on adult wintering
grounds (Earnst 2004, p. 11), might be
exposed to commercial fisheries
overlapping these areas year-round.
Adult yellow-billed loons could be
exposed to commercial fisheries on the
wintering grounds and over a larger area
of marine coastlines during migration,
as well as to subsistence fishing during
migration and while on the nesting
grounds.
I. Commercial Fishing Bycatch
Loon bycatch has been documented in
commercial drift-net, gill-net, trap-net,
and longline fisheries. Compared to
other fisheries, gill-net fisheries have
the greatest potential to affect loons. For
example, a 1998 study of bycatch in
winter gill-net fisheries on the U.S. midAtlantic coast found that loons (redthroated and common) accounted for 89
percent of all avian bycatch (Forsell
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1999, p. 23). While loon species have
been recorded as bycatch in several
longline fisheries (Brothers et al. 1999),
in general, longlines attract surfacefeeding seabirds rather than species that
dive to feed.
While commercial fishing occurs
across marine waters inhabited by
yellow-billed loons, primarily within
the species’ wintering grounds, there are
several challenges to assessing the
impact of these fisheries on the species.
Bycatch monitoring programs are
infrequent and do not exist for many
fisheries in the yellow-billed loon’s
wintering grounds. This is particularly
true for the Yellow Sea, which is
historically one of the most intensively
fished areas in the world (LME 48 2004,
p. 1). Where programs do exist, loons
are often not identified to species level
or are categorized as ‘‘other.’’ These
problems might explain low reported
levels of yellow-billed loon bycatch. In
addition, actual bycatch in any given
fishery is likely to be low due to the
species’ low densities and widespread
distribution.
Alaska
The Alaskan commercial fisheries
most likely to catch yellow-billed loons
are gill-net fisheries in the Gulf of
Alaska (Prince William Sound and Cook
Inlet) and Southeast Alaska. While these
fisheries overlap spatially with areas
used by yellow-billed loons, they occur
primarily during summer when adults
and an unknown proportion of
immatures have moved north to arctic
habitats.
No bycatch data are available from
gill-net fisheries in Southeast Alaska,
but limited seabird bycatch data are
available from some Gulf of Alaska
fisheries with marine mammal bycatch
monitoring programs. For example,
salmon gill-net fisheries in Prince
William Sound and Unimak Island area
in 1990 to 1991 recorded low levels of
loon bycatch (1 unknown loon, 2 redthroated loons, and 2 common loons
from more than 9,000 sets; Wynne et al.
1991, p. 30; Wynne et al. 1992, pp. 47–
48). Another program for Cook Inlet
salmon drift-net and set-net fisheries
(1999–2000) also recorded low loon
numbers (2 common loons and 1
unidentified loon in 540 sets observed;
Manly 2006, pp. 27 & 32). Of all loons
observed near nets in 2000, about half
were identified as common loons, and
half were unknown loon species (Manly
2006, p. 40).
Alaska longline, pot, and trawl
fisheries are less likely to affect this
species due to the loon’s foraging
behaviors and location of these
fisheries. While these fisheries overlap
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12957
the wintering grounds of the yellowbilled loon in the Bering Sea, Aleutians,
and Gulf of Alaska from September to
April, they are conducted offshore. An
observer program exists for the Alaskan
demersal groundfish fisheries (including
longline, pot, and trawl for certain
groundfish species) but no loon bycatch
data exist because all loon species are
classified as part of the category ‘‘other’’
along with several other species not
typically caught by these gear types.
Less than one percent (0–351 individual
birds) of all reported bycatch in these
fisheries has been recorded as ‘‘other’’
for years 1993 through 2006 (AFSC
2006a, pp. 9–15; AFSC 2006b, pp. 5–8;
AFSC 2007, pp. 5–9). In addition,
bycatch rates in the longline fisheries
have declined in recent years (highs in
1998–1999) due to the implementation
of seabird-avoidance measures (AFSC
2006a, p. 2).
In summary, bycatch of loon species,
as well as unknown loons, has been
reported in limited observer-program
coverage of Alaskan gill-net fisheries
that occur within the yellow-billed
loon’s range. While no bycatch of
yellow-billed loons has been reported,
available data are limited and lacking
for some parts of the species’ range. In
addition, there is no available
information that suggests take levels
will change in the future.
Washington State and British Columbia
Loon entanglement has been reported
in commercial gill-net fisheries in
Washington’s Puget Sound, Hood Canal,
Willapa Bay, Grays Harbor, and the
Columbia River. At least 1 yellow-billed
loon, 3 unidentified loons, and 11
common loons were documented as
bycatch in the mid-1990s (Erstad et al.
1994, p. 6; Pierce et al. 1994, p. 18;
Erstad et al. 1996, p. 12; and Jeffries et
al. 1996, cited in Richardson et al. 2000,
p. 20). Based on season, these birds are
presumably non-breeders. Fishery-wide
estimates were not extrapolated.
In British Columbia, common and
Pacific loons have been identified as
bycatch in sockeye gill net fisheries, but
comprise less than one percent of total
bycatch reported from net fisheries from
1995–2001 (one individual of each
species was identified, for an estimated
take of 31 of each species) (Smith and
Morgan 2005, p. 25) (although a high
proportion of bycatch was unidentified).
Based upon known seabird and
commercial fishing locations, Queen
Charlotte Sound, the Scott Islands, and
Cape St. James are of concern for
bycatch from March–June, and the
Western coast of Vancouver Island from
June–September (Smith and Morgan
2005, p. 29). These areas are all in
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yellow-billed loon wintering grounds,
and non-breeding yellow-billed loons
might remain there throughout summer.
In summary, bycatch of loon species,
including one yellow-billed loon, has
been reported in limited observerprogram coverage of Washington and
British Columbia gill-net fisheries that
occur within the yellow-billed loon’s
range. The available data indicate that
individuals (particularly non-breeders)
are vulnerable to bycatch in these
fisheries, but do not allow estimation of
the number of yellow-billed loons taken.
We also have no information to predict
whether current take levels will increase
or decrease in the future.
Russian Far East
Russian drift-net fisheries for salmon,
as well as net fisheries for herring,
mackerel, and Pacific saury occur in the
northwest Pacific Ocean (Northridge
1991, p. 52). Bycatch data do not exist
for most of these fisheries (WWF 2004,
p. 56), except for limited data from the
salmon drift-net fisheries. Seabird
bycatch was monitored for the Japanese
salmon drift-net fishery in the Russian
Exclusive Economic Zone within the
Sea of Okhotsk and Kuril Islands from
1993 to 1998 and western Bering Sea
from 1993 to 2001. This fishery takes
place from May through July. Yellowbilled loons comprised less than or
equal to 0.02 percent of reported
bycatch, with an extrapolated estimate
of 89 yellow-billed loons, likely nonbreeders, within all fishery zones from
1993–1998, and an additional 45
individuals in the Bering Sea zone from
1999–2001 (Artukhin et al. 1999, pp. 96
& 101; Artukhin et al. 2000, p.122;
Artukhin et al. 2001, p. 83). The highest
bycatch rate (0.4 percent) for all fishery
zones occurred in the area bordering the
Northern edge of the Sea of Okhotsk
(from 1993 to 1998) (Artukhin et al.
1999, p. 96; Artyukhin and Burkanov
2000, p. 108). Overall, catch rates of
yellow-billed loons were similar to but
slightly higher than those reported for
other loons (arctic and red-throated).
Unidentified birds comprised less than
or equal to 0.05 percent of bycatch. No
yellow-billed loons have been reported
as bycatch in the Russian salmon driftnet fishery (Y. Artukhin in litt. 2008, p.
1), which exceeded the Japanese salmon
harvest in 2003 (WWF 2004, p. 56).
Longline and trawl fisheries also
occur in the Russian Far East by
Russian, Japanese, Korean, and
American companies (Artyukhin et al.
2006, p. 7). These year-round fisheries
for cod, halibut, and rockfish are located
primarily in western Bering Sea, Pacific
Ocean waters of Kamchatka, and Sea of
Okhotsk (Artyukhin et al. 2006, p. 6). A
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seabird observer program for the
Russian longline fishery was conducted
in these waters from 2003 to 2005
during a project to test methods and
equipment to reduce incidental seabird
bycatch (Artyukhin et al. 2006). No
loons were reported as bycatch
(Artyukhin et al. 2006, p. 19).
In summary, yellow-billed loon
bycatch has been reported in drift-net
fisheries within the Sea of Okhotsk and
the western Bering Sea. Due to the
timing of the fisheries, most individuals
were likely non-breeders. The data
indicate vulnerability of the species to
incidental capture in drift-net gear, but
do not allow estimation of the total
number of yellow-billed loons taken. In
addition, there is no available
information that suggests take levels
will change in the future.
Yellow Sea, Sea of Japan, and Coastal
Japan
The Yellow Sea, one of the most
heavily fished areas of the world, is
classified by the Global International
Waters Assessment as severely affected
by overfishing, with major fisheries
currently occurring at a low level
compared to 30 years ago (LME 48
2004). Both the Yellow Sea and Sea of
Japan are primarily fished by Japan,
China, Korea, and the Russian
Federation nearshore gill-net fleets
(Northridge 1991, pp. 52–54; LME 48
2004; LME 50 2004). There are also a
considerable number of Japanese gill-net
fishing vessels in Japanese coastal
waters, with coastal vessels estimated to
be in the thousands (DeGange et al.
1993, p. 207). Various gill-net fisheries
(i.e., Spanish mackerel (Scomberomorus
niphonius), silver pomfret (Pampus
argenteus), and Chinese herring (Illisha
elongata)) occur during different
months of the year (Northridge 1991,
pp. 53 & 54; Zhang and Kim 1999, p.
167), including overlap in time and
location with non-breeders and adult
wintering yellow-billed loons. The level
of seabird bycatch from most of these
coastal fisheries is unknown (DeGange
et al. 1993, p. 209). Longline fisheries
conducted by Japan, China, and the
Republic of Korea are also known to
occur (Brothers et al. 1999), but bycatch
information is unavailable.
In summary, no data are available on
the level of yellow-billed bycatch from
gill-net fisheries in the Yellow Sea, Sea
of Japan, or coastal Japan. Due to the
vulnerability of the species to incidental
capture in gill nets and extensive
activity of these fisheries overlapping in
timing and location with the loon’s
adult wintering range, bycatch likely
occurs. However, we have no means to
assess the current level of take. In
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addition, there is no available
information that suggests take levels
will change in the future.
Norway
Fisheries occur along the entire
coastline of Norway, with northern
areas most intensively fished (Bakken
1998, p. 28). Atlantic cod (Gadus
morhua) is the most important fishery,
and other species fished include
capelin, flatfish, haddock, herring,
lumpsucker, and salmon (Bakken 1998,
p. 28). The Lofoten fishery, a major
fishery that includes one-fifth of
Norway’s total fishermen, primarily
targets Atlantic cod, from February to
April, and uses both gill nets and long
lines, along with hand lines and seines
(Jentoft and Kristoffersen 1989, pp. 356–
357). Limited data exist on seabird
bycatch in these fisheries, but loons
have been reported as bycatch in the
cod, herring, haddock, and flatfish gillnet fisheries all along the Norwegian
coast (Bakken 1998, pp. 28 & 36). There
are anecdotal reports of yellow-billed
and common loon bycatch in gill nets,
especially in the Lofoten Islands, and in
Troms County to a lesser extent (Strann
and ;stnes 2007, p. 4). Although the
extent of winter bycatch is unknown,
Strann and ;stnes (2007, p. 4) suggest,
based on anecdotal observations, that
take of yellow-billed and common loons
might be increasing in the Lofoten
Islands.
In summary, yellow-billed loons, as
well as other loon species, have been
anecdotally reported as bycatch in
Norwegian gill-net fisheries. We have no
means to extrapolate available
information to estimate the total number
of yellow-billed loons taken. In
addition, other than anecdotal
information that suggests take levels in
the Lofoten Islands are increasing, we
do not have evidence that take levels
will change in the future.
II. Subsistence-Fishing Bycatch
Subsistence fishing is an important
component of the customs, traditions,
and economies of many indigenous
groups in the arctic. Across the breeding
range of the yellow-billed loon, rural
residents fish primarily using gill nets,
although some angling and ice jigging
occurs (Craig 1987, p. 17). Gill-net use
is localized near villages and fish
camps, in marine inlets and lagoons,
lakes, and rivers, depending on season
and target fish species (Craig 1987, p.17,
Bacon in litt. 2008). During the breeding
season, yellow-billed loons will forage
in large lakes close to their nests (Earnst
2004, p. 4), as well as other nearby
lakes, rivers, and marine areas (Earnst
2004, pp. 6–7), where the potential for
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bycatch in subsistence fisheries exists.
Because yellow-billed loons are widely
dispersed across their nesting grounds,
however, a large proportion of the
breeding population is likely not
exposed to localized subsistence fishing.
Limited observations confirm that
yellow-billed loons have been
inadvertently caught in subsistence gill
nets in Canada, Russia, and the United
States, although the level of bycatch is
not extensively documented. In Canada,
researchers on Victoria Island
documented yellow-billed loon
entanglement in nets on several
occasions, including one instance where
seven birds were found dead in nets in
a single day (Sutton 1963 p.1; Parmelee
et al. 1967). In Russia, Syroechkovski
(2008, p. 2) reported that two reasons for
subsistence harvest were accidental
entanglement in fishing nests and
deliberate shooting to scare loons from
fishing areas. The Red Data Book of the
Russian Federation states that yellowbilled loon mortality in fishing nets is
the main threat to the species (Red Data
Book 2001, pp, 366–367), with bycatch
rates described as ‘‘catastrophic’’ in the
Chukchi Peninsula region (Red Data
Book 2001, pp, 366–367). We could not
locate data or a source for that
assessment.
In Alaska, information on loon
bycatch from subsistence fishing is
available only for the ACP, where
Inupiat Eskimos use yellow-billed loon
parts for subsistence and ceremonial
purposes (Hepa and Bacon 2008, p. 1).
With implementation of Alaska spring/
summer migratory bird subsistenceharvest regulations in 2003, the yellowbilled loon was officially closed to
harvest (Hepa and Bacon 2008, p. 1).
In 2005, an exception for the North
Slope region was incorporated into the
regulations allowing possession for
subsistence use of up to 20 (total for the
region each year) yellow-billed loons
inadvertently caught in subsistence nets
(50 CFR Part 92). As a result of this
provision, the North Slope Borough
Department of Wildlife Management
compiles data on incidental bycatch
from a variety of sources. Two to nine
yellow-billed loons (and some redthroated and Pacific loons) were
reported as found dead in nets in each
of three years (2005 to 2007) (Acker and
Suydam 2006, p. 1; Acker and Suydam
2007, p. 1; Hepa and Bacon 2008, p. 10).
Small numbers of loons, including
yellow-billed loons, were also reported
as found alive and released. All yellowbilled loons collected in 2007 were
reportedly utilized for subsistence,
including ceremonial purposes (Hepa
and Bacon 2008, p. 2). These numbers
are likely a minimum estimate of
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yellow-billed loon subsistence bycatch
because not all fishers were contacted
(Hepa and Bacon 2008, p. 2).
In conclusion, yellow-billed loon
bycatch in commercial fisheries has
been documented anecdotally or by
observer programs in Washington State,
Russia, and Norway. No data exist from
large portions of the species’ wintering
range (Yellow Sea, Sea of Japan, and
coastal Japan), but bycatch is likely to
occur in extensive gill net fisheries that
overlap with wintering yellow-billed
loons. We lack information to explain
the difference in catch rates reported
from various observer programs. We do
not have enough information to
extrapolate bycatch estimates to areas
lacking data, or to determine the
number of birds taken as bycatch over
time.
For subsistence fisheries, yellowbilled loon bycatch has been
documented either anecdotally or in
reporting programs on the breeding
grounds in Alaska, Canada, and Russia.
Data are limited or non-existent for large
parts of the species’ range. Because
yellow-billed loons are widely
dispersed across the landscape on the
nesting grounds, while subsistence
fishing is localized, we suspect a large
proportion of the breeding population is
not exposed to subsistence fishing. We
do not have enough information to
extrapolate subsistence bycatch
accounts to areas lacking data or to
evaluate likely population-level affects.
Yellow-billed loon bycatch data are
primarily anecdotal and cannot be
extrapolated to estimate total bycatch
levels or rates. Although yellow-billed
loon mortality from commercial and
subsistence gill-net fisheries currently
affects yellow-billed loons at the
individual level, we do not have enough
evidence of bycatch to show populationlevel impacts. The ACP breeding
population is the only one for which we
have trend information. That trend is
slightly declining or stable, and so we
do not have evidence that bycatch is
currently affecting the species at the
population level. In addition, there is no
available information that suggests take
levels will change in the future.
Therefore, we find that bycatch is not a
threat to yellow-billed loons now or in
the foreseeable future.
Direct Effects of Contaminants Not
Associated With Oil and Gas
Although contaminants can affect
species through a variety of
mechanisms, below we discuss direct
effects on individuals or reproduction,
such as mortality or embryo viability,
from contaminants other than those
associated with oil and gas (discussed
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12959
under Factor A and earlier in Factor E).
Indirect effects of contaminants or
pollution, such as alterations in prey
abundance, were also discussed under
Factor A.
Ecological characteristics can be used
to estimate the relative risk of
contaminants to a species. These
include trophic status (species higher in
a food chain are more likely to
accumulate persistent pollutants),
pollution point sources, location
(including migratory pathways), and
lifespan (long-lived individuals have
more time to accumulate persistent
compounds). Yellow-billed loons are
relatively long-lived birds, and being
piscivorous are also trophically
elevated. Both arctic breeding areas and
temperate wintering areas have
documented pollution. It is therefore
appropriate to examine potential risk to
yellow-billed loons from contaminant
exposure.
Yellow-billed loons spend the
majority of the year in southern
wintering areas, which are primarily
coastal and are more likely to have
elevated environmental concentrations
of persistent organic pollutants (POPs),
such as organochlorine pesticides and
polychlorinated biphenyls (PCBs),
compared to northern breeding areas.
Twenty-four out of 29 yellow-billed
loons fitted with transmitters on Alaska
breeding grounds wintered in Asian
waters (Schmutz 2008, p. 1) that have
been demonstrably affected by
pollution. For example, Ma et al. (2001,
pp. 133–134) reported high levels of
persistent organic pollutants (DDT and
PCBs) and petroleum-derived
contaminants in the intertidal zone of
the Bohai and Yellow Seas off China. In
Korea, PCBs were greater in fish and
birds from industrially contaminated
areas of the Nakdong estuary than nonindustrial areas (Choi et al. 1999, p.
233). Other studies document
contamination of Asian sea sediments
and biota, including fish and birds, that
support potential exposure for wintering
migratory birds such as yellow-billed
loons (e.g., Nie et al. 2005, pp. 537–546;
Oh et al. 2005, pp. 217–222; Daoji and
Daler 2004, pp. 107–113; Guruge et al.
1997, pp. 186–193). In a test of exposure
to persistent contaminants in Asian
wintering areas compared to northern
breeding areas, Kunisue et al. (2002, p.
1,397) found that herring gulls (Larus
argentatus) and other migratory birds
nesting on Lake Baikal in Russia had
higher levels of organochlorine
contaminants on arrival from Asian
wintering areas than at the end of the
breeding season.
Further, sympatrically nesting redthroated loons from the ACP had PCB
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concentrations and formulations
(containing the most toxic PCB
congeners) great enough, when
compared to thresholds developed for
other species, to postulate teratogenic
(causing abnormal development) or
other reproductive effects (Schmutz et
al. in review, p. 19). Preliminary
satellite telemetry data indicate that
these red-throated loons winter in Asian
marine waters (Schmutz et al. in review,
p. 1), similar to yellow-billed loons.
These data compelled us to examine
PCBs in yellow-billed loon eggs from
the ACP. We found that although PCBs
were present in yellow-billed loon eggs
(n = 45, collected over three years),
preliminary data show the most toxic
individual PCB congeners (PCBs 77 and
81) present in red-throated loon eggs
were generally not present in yellowbilled loon eggs, and therefore the PCB
toxicity in yellow-billed loon eggs (TEQ
(toxic equivalency quotient, a measure
of toxicity) range = 0.176—10.39
picograms/gram (pg/g); A. Matz, U.S.
Fish and Wildlife Service, unpubl. data)
was much lower than in red-throated
loon eggs (TEQ mean ± SE = 237 ± 129
pg/g), and lower than published
thresholds for embryonic toxicity in
other avian species, such as 227 pg/g in
great blue heron (Ardea herodias) eggs
(Hoffman et al. 1996, pp. 191). We are
currently evaluating other contaminants
in yellow-billed loon eggs and blood
from the coastal plain and the Seward
Peninsula of Alaska, but based on the
red-throated loon data (presented in
Schmutz et al. in review), we were most
concerned about the PCBs.
In conclusion, we have few data on
most of the contaminants that could
directly affect yellow-billed loons
throughout their range. Additional
range-wide data on productivity,
population trends, and concentrations
of persistent contaminants will allow us
to more fully evaluate this risk factor.
However, data from an ongoing multiagency study in Alaska show that
yellow-billed loon eggs do not have
concentrations of toxic PCBs thought to
affect reproduction. Because yellowbilled loons nesting in Canada, and
some proportion of those nesting in
Russia, likely winter in Asian seas or on
the Pacific coast of North America, we
assume that PCB and other persistent
contaminant concentrations in their
eggs would be equal to or less than
those from the ACP, which are known
to winter in Asia. The contaminant
loading for yellow-billed loons
wintering in the North Sea is unknown,
but those loons represent a small
proportion of the total population. In
the future, yellow-billed loons could
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continue to be exposed to the
contaminants they are exposed to now,
as well as emerging persistent
contaminants such as polybrominated
compounds. However, the Service and
its partners plan to monitor contaminant
exposure, mortality, and productivity in
Alaska. Future contaminant risks will be
identified and efforts made to address
them before they cause population-level
declines that threaten the continued
existence of the species. Therefore, we
find that contaminants other than those
associated with oil and gas are not a
threat to the yellow-billed loon now or
in the foreseeable future.
In our analysis of Factor E, we
identified and evaluated other risk
factors, including: Oil and gas
development and vessel traffic;
subsistence harvest; commercial- and
subsistence-fishery bycatch; and
contaminants other than those
associated with oil and gas. Based on
our review of the best available
information, we find that subsistence
harvest is a threat to the yellow-billed
loon now and in the foreseeable future.
Foreseeable Future
In considering the foreseeable future
as it relates to the status of the yellowbilled loon, we considered the stressors
acting on the species. We considered the
historical data to identify any relevant
existing trends that might allow for
reliable prediction of the future (in the
form of extrapolating the trends). We
also considered whether we could
reliably predict any future events that
might affect the status of the species,
recognizing that our ability to make
reliable predictions in the future is
limited by the variable quantity and
quality of available data. Further,
predictability varies significantly among
risk factors, and in some cases, even
geographically within a single factor.
Based on the lack of proposed
onshore oil and gas development within
the yellow-billed loon’s range in
Canada, it is reasonably likely that no
population-level impacts will be
incurred at least until development
occurs. In contrast, in Russia, although
it is likely that oil and gas development
will increase in the future, our
understanding of the species’
distribution is so limited that it is
difficult to reliably assess the likely
impact of even existing oil and gas
development on the yellow-billed loon,
much less the impact of projected future
development on the loon. In Alaska,
some increased terrestrial oil and gas
development is likely to occur
beginning in the next decade, and the
period from exploration through
production to abandonment is estimated
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at 70 years. In the case of climate
change, current models suggest that
global temperatures are likely to
continue to rise for up to 50 years, even
if greenhouse gas emissions were curbed
today (Meehl et al 2007, p. 749).
However, we are not currently able to
link projected climate changes to
changes in arctic freshwater habitats or
their ability to support loons, and so our
ability to foresee the future is limited
until research and climate modeling
improve our predictive ability.
Although climate-change models show
continued decrease in the summer arctic
ice sheet, and it is possible that
shipping will, therefore, increase, we
have no data to describe to what degree
shipping pathways or frequency is
likely to change. With respect to
subsistence harvest, the best available
data show substantial inter-annual
variation in loons harvested in Alaska
during migration, which could be
related to inter-annual variation in
yellow-billed loon migratory behavior.
Modeled scenarios show that even when
harvest varies among years within the
range defined by recent harvest
estimates, the yellow-billed loon
population continues to decline over
time. Although we have no information
that subsistence harvest throughout the
range of the yellow-billed loon will
either increase or decrease in the future,
we have no reason to believe that
harvest of yellow-billed loons will not
continue to vary from year to year
within the range of levels incurred over
recent years. Our ability to assess
current bycatch in fishing nets is limited
by poor data, and we have no empirical
basis with which to predict even the
direction of trends in the effects of this
activity into the future. Although the
amount of oil and gas development and
shipping traffic will likely increase in
the future, the associated risk is
reasonably likely to be partly or wholly
offset by improved technologies and
regulation. We do not have evidence
that marine pollution or contaminants
will have an increased or decreased
effect on yellow-billed loons in the
future.
Available data indicate a stable or
slightly declining trend for the ACP
population. Available data do not allow
us to establish a trend for other breeding
populations. Overall numbers of yellowbilled loons are cautiously estimated
between 16,000 and 32,000 birds on
breeding grounds worldwide, which,
considering the wide distribution of the
species most of the year, is enough to
make it unlikely that the species is at
risk from stochastic events because of its
small numbers. Thus, the foreseeable
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Finding
future includes consideration of the
ongoing effects of current risk factors
and threats at comparable levels.
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Significant Portions of the Range
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.’’ The term ‘‘significant portion
of its range’’ is not defined by the
statute. For the purposes of this finding,
a significant portion of a species’ range
is an area that 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 to conserve the species.
If an analysis of whether a species is
threatened or endangered in a
significant portion of its range is
appropriate, we engage in a systematic
process that begins with identifying 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 only 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 or likely to
become so within the foreseeable future.
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.
On the basis of an analysis of factors
that may threaten the yellow-billed
loon, we have determined that listing is
warranted throughout its range.
Therefore, it is not necessary to conduct
further analysis with respect to the
significance of any portion of its range
at this time. We will further analyze
whether threats may be disproportionate
and warrant further consideration as an
SPR at such time that we develop a
proposed listing determination.
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In our review of the status of the
yellow-billed loon, we carefully
examined the best scientific and
commercial information available. We
identified a number of potential threats
to this species, including: Oil and gas
development, marine pollution and
overfishing, exposure to contaminants,
climate change, subsistence- and
commercial-fishing bycatch, and
subsistence harvest. To determine
whether these risk factors individually
or collectively put the species in danger
of extinction throughout its range, or are
likely to do so within the foreseeable
future, we first considered whether the
risk factors were causing a population
decline, or were likely to do so in the
future.
Information on population size and
trends for the yellow-billed loon is
limited. Overall population size is
unknown, but probably at the low end
of the range between 16,000 and 32,000
loons on breeding grounds. Population
trends are available for the ACP
breeding grounds from waterfowl
surveys, and these surveys suggest that
the ACP breeding population is stable or
slightly declining. Limited surveys have
been conducted only in small parts of
the Russian and Canadian ranges, so
population sizes for these ranges are
gross approximations, and no
information on trends is available.
There are reports of range contractions
at the edges of the Russian breeding
range, but these reports are
unsubstantiated, and there are also
unsubstantiated reports of Russian
breeding areas where yellow-billed loon
numbers could be increasing. Therefore,
based on the best available information,
we find that the only trend information
we have indicates a stable or slightly
declining trend for the ACP population.
We evaluated existing and potential
stressors on the yellow-billed loon to
determine what affects on the species
were currently occurring, whether these
stressors were likely to increase or
decrease in the future, and which of the
stressors may be expected to rise to the
level of a threat to the species, either
rangewide or at the population level.
We examined several stressors for
which we have little information on
whether they will increase in the future.
We did not find that bycatch by
subsistence or commercial fishing,
pollution in wintering habitats, or
contaminants are threats to the yellowbilled loon. An unknown number of
individuals are taken in fisheries, which
adds to other forms of mortality.
Next we considered whether any of
the risk factors are likely to increase
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12961
within the foreseeable future. We
believe that oil and gas activities in
various parts of the loon’s range are
likely to increase in the future. In
Alaska, we determined that Federal and
State of Alaska regulations currently in
place will likely mitigate future effects
of terrestrial oil and gas development,
and therefore development in Alaska is
not considered a threat to the species
now or in the foreseeable future. In
Russia, terrestrial oil and gas
development is occurring at the western
edge of the Russian breeding range, and
it is unknown whether this activity
overlaps with loon nesting habitat. Most
importantly, even if a local range
contraction has occurred, we find no
reason to conclude impacts extend
beyond the local scale at the edge of the
range. In Canada, there has been little
overlap between oil and gas
development and the species’ range, and
we are aware of none projected for the
near future. We also found that although
marine oil and gas development is likely
to increase in various parts of the loon’s
range, the wide distribution and low
density of the species in the marine
environment make it unlikely that
associated impacts including marine oil
spills will put the species at risk of
extinction.
Climate change is likely to continue
for at least the next 50 years, but there
is substantial uncertainty as to how
climate change, described in Factor A,
will affect yellow-billed loon terrestrial,
freshwater, and marine habitats. For
example, if native prey fish species are
extirpated, other suitable prey species
may colonize the area, replacing
extirpated species to some degree. We
do not know whether large-scale
degradation of continuous permafrost,
where the majority of yellow-billed
loons breed, and the subsequent impacts
to lake levels and vegetation will occur
on a scale that will affect loon
populations in the foreseeable future.
Climate-change effects on the temperatelatitude wintering habitat of the yellowbilled loon include increases in ocean
temperature and decreases in primary
productivity and dissolved oxygen
levels, which might affect numbers and
distribution of prey species. The
magnitude and form of these effects are
highly uncertain, but would most likely
involve northward shift of prey items,
which could be mirrored by their
predators such as wintering yellowbilled loons.
There are multiple hypothetical
mechanisms associated with climate
change that could potentially affect
loons and their breeding and nonbreeding habitats. Unlike documented
and predicted declines in sea ice, an
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obligate habitat for other arctic species
such as polar bears, we lack predictive
models on how climate change will
affect yellow-billed loon terrestrial,
freshwater, and marine habitats.
Manifestations of climate-mediated
changes throughout arctic and
temperate yellow-billed loon habitats
will emerge if reliable, predictive
models are developed, but currently
there is little certainty regarding the
timing, magnitude, and net effect of
impact. Therefore, given current
limitations in available data and climate
models, we find that climate change is
not a threat to yellow-billed loons now
or in the foreseeable future. However,
currently unknown detrimental effects
of climate change could be additive to
other threats and stressors on the
population.
We also considered whether any of
the ongoing risk factors began recently
enough that their effects are not yet
manifested in a long-term decline in
population numbers, but are likely to
have that effect in the future.
Information from recent subsistence
harvest surveys indicate potentially
high levels of harvest compared to
earlier surveys. There are not enough
years of data, and there is not enough
precision in the accuracy of the surveys,
to indicate whether there is a trend of
increasing harvest. All marked Alaskan
breeding birds used the Bering Strait or
Chukotka Peninsula during migration;
in addition, it is likely that most
Russian breeding loons and at least
some Canadian breeding birds also
migrate through the Bering Strait region.
Thus, we believe it is likely that a large
part of the rangewide population moves
through the Strait and is subject to
harvest there. The best available
information indicates that, on average,
hundreds of yellow-billed loons from
breeding areas throughout its range are
harvested annually by subsistence
hunters. Population modeling suggests
that the number of yellow-billed loons
being harvested in the Bering Strait area
of Alaska alone is likely unsustainable.
The lack of precision of the population
trend information for Alaska could be
preventing us from detecting the impact
of this harvest on the population, or the
high harvest estimates could represent a
new phenomenon not yet taken into
account in our population trend
estimates. The harvest is also likely
having an impact on breeding
populations that are not being
monitored in Canada and Russia.
Because we believe that the rangewide
population of yellow-billed loons is
subject to unsustainable levels of
harvest, we find that subsistence harvest
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is a threat to the species rangewide. In
light of this level of subsistence harvest
occurring despite existing MBTA
regulations that prohibit such harvest,
we also find that inadequate regulatory
mechanisms are a threat to the species.
We next considered whether the
existing level of threats causes us to
conclude that the species is in danger of
extinction now or in the foreseeable
future. If population size were to
decline or the range were to contract,
recovery or re-colonization would likely
occur slowly. Individuals in the
population are so widespread during
most of the year that high adult
mortality is unlikely. However, during
migration, yellow-billed loons are
subject to subsistence harvest that
appears to be unsustainable based on
the best available information. The total
population is uncertain, but based on
the best available information, the
population, estimated at 16,000 to
32,000 birds on breeding grounds, could
decline substantially if unsustainable
harvest continues. Future subsistence
harvest in Alaska is enough in itself to
constitute a threat to the species
rangewide. In addition, up to several
hundred yellow-billed loons could be
taken annually on Russian breeding
grounds, and small amounts of harvest
are reported for other areas in Alaska
and Canada. Other stressors discussed
above may not rise to the level of a
threat individually, but when taken
collectively with the effects of
subsistence hunting in other areas, may
reduce the rangewide population even
further. Given the small population and
the existence of subsistence harvest and
inadequate regulatory mechanisms as
threats, we believe the species is likely
to become in danger of extinction
within the foreseeable future. Therefore,
we find that listing the yellow-billed
loon throughout its range is warranted.
While we find that listing the yellowbilled loon is warranted, an immediate
proposal to list this species is precluded
by other higher priority listing actions,
which we address below.
We have reviewed the available
information to determine if the existing
and foreseeable threats pose an
emergency. We have determined that an
emergency listing is not warranted for
this species at this time because, within
the current distribution of the species
throughout its range, there are at least
some populations of the yellow-billed
loon that exist in relatively natural
conditions that are unlikely to change in
the short-term. However, if at any time
we determine that emergency listing of
the yellow-billed loon is warranted, we
will initiate an emergency listing.
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Future Conservation
We have determined that the listing of
the yellow-billed loon is warranted but
precluded by pending proposals for
other species with higher listing
priorities and actions. Our
recommendation of a listing priority
number of 8 (described below) will
provide time and opportunity to
implement conservation and better
monitor the species’ status and threats.
Here we provide a summary of our
commitment to the conservation of
yellow-billed loons.
As described in the ‘‘Conservation
Agreement for the Yellow-billed Loon
(Gavia adamsii),’’ the Service and its
partners plan to: (1) Implement specific
actions to protect yellow-billed loons
and their breeding habitats in Alaska
from potential impacts of land uses and
management activities, including oil
and gas development; (2) inventory and
monitor yellow-billed loon breeding
populations in Alaska; (3) reduce the
impact of subsistence activities
(including fishing and hunting) on
yellow-billed loons in Alaska; and (4)
conduct biological research on yellowbilled loons, including response to
management actions.
We believe that the strategies outlined
in the agreement demonstrate the
partners’ commitment to prioritize
yellow-billed loon conservation in
Alaska. To fulfill the first strategy, we
will continue to work with partners to
maintain their commitment to actions
protecting loons. In particular, we will
work closely with the BLM to monitor
and maintain protection of loons on
NPR-A, as expressed in their recent
memorandum on the yellow-billed loon
(Galterio, in litt. 2008, pp. 1–3). For the
second strategy, we will continue to
inventory yellow-billed loons through
our waterfowl surveys on the ACP and
through loon-specific surveys currently
in operation on the Seward Peninsula,
and we will investigate the potential for
initiating yellow-billed-loon-specific
surveys. For the third strategy, we are
working closely with the Alaska
Migratory Bird Co-management Council
(AMBCC) and the State of Alaska to
acquire reliable, verifiable information
on subsistence harvest and fishing
bycatch levels in Alaska, and to
substantially increase education and
law enforcement efforts to reduce levels
of this threat. Finally, we support the
ongoing research by the U.S. Geological
Survey and others on yellow-billed
loons in Alaska, and will continue to
advocate for further research where it
will inform management of yellowbilled loons, such as understanding
effects of disturbance on nesting loons
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to ensure that buffers separating loons
from human activity are adequate.
Research and management of yellowbilled loons are needed outside Alaska,
and we will support and advocate for
such work. In particular, we need to
understand population sizes and trends
for Russian and Canadian breeding
populations, migration corridors, and
where breeding populations winter. We
also encourage managers in both
countries to take an active role
conserving loons where substantial
industrial development occurs, or where
other threats such as subsistence harvest
or fishing bycatch occur. Finally, habitat
conditions in wintering grounds,
especially in Asia, need to be
understood and managed so that they
continue to support loons. In particular,
it will be critical to increase awareness
of pollution impacts in marine habitats
in Asia, and to develop regulations to
reduce pollution levels, so that these
wintering areas continue to support
yellow-billed loons.
Preclusion and Expeditious Progress
Preclusion is a function of the listing
priority of a species in relation to the
resources that are available and
competing demands for those resources.
Thus, in any given fiscal year (FY),
multiple factors dictate whether it will
be possible to undertake work on a
proposed listing regulation or whether
promulgation of such a proposal is
warranted but precluded by higherpriority listing actions.
The resources available for listing
actions are determined through the
annual Congressional appropriations
process. The appropriation for the
Listing Program is available to support
work involving the following listing
actions: proposed and final listing rules;
90-day and 12-month findings on
petitions to add species to the Lists of
Endangered and Threatened Wildlife
and Plants (Lists) or to change the status
of a species from threatened to
endangered; annual determinations on
prior ‘‘warranted but precluded’’
petition findings as required under
section 4(b)(3)(C)(i) of the Act; proposed
and final rules designating critical
habitat; and litigation-related,
administrative, and program
management functions (including
preparing and allocating budgets,
responding to Congressional and public
inquiries, and conducting public
outreach regarding listing and critical
habitat). The work involved in
preparing various listing documents can
be extensive and may include, but is not
limited to: gathering and assessing the
best scientific and commercial data
available and conducting analyses used
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as the basis for our decisions; writing
and publishing documents; and
obtaining, reviewing, and evaluating
public comments and peer review
comments on proposed rules and
incorporating relevant information into
final rules. The number of listing
actions that we can undertake in a given
year also is influenced by the
complexity of those listing actions; that
is, more complex actions generally are
more costly. For example, during the
past several years, the cost (excluding
publication costs) for preparing a 12month finding, without a proposed rule,
has ranged from approximately $11,000
for one species with a restricted range
and involving a relatively
uncomplicated analysis to $305,000 for
another species that is wide-ranging and
involving a complex analysis.
We cannot spend more than is
appropriated for the Listing Program
without violating the Anti-Deficiency
Act (see 31 U.S.C. 1341(a)(1)(A)). In
addition, in FY 1998 and for each fiscal
year since then, Congress has placed a
statutory cap on funds which may be
expended for the Listing Program, equal
to the amount expressly appropriated
for that purpose in that fiscal year. This
cap was designed to prevent funds
appropriated for other functions under
the Act (for example, recovery funds for
removing species from the Lists), or for
other Service programs, from being used
for Listing Program actions (see House
Report 105–163, 105th Congress, 1st
Session, July 1, 1997).
Recognizing that designation of
critical habitat for species already listed
would consume most of the overall
Listing Program appropriation, Congress
also put a critical habitat subcap in
place in FY 2002 and has retained it
each subsequent year to ensure that
some funds are available for other work
in the Listing Program: ‘‘The critical
habitat designation subcap will ensure
that some funding is available to
address other listing activities’’ (House
Report No. 107–103, 107th Congress, 1st
Session, June 19, 2001). In FY 2002 and
each year until FY 2006, the Service has
had to use virtually the entire critical
habitat subcap to address courtmandated designations of critical
habitat, and consequently none of the
critical habitat subcap funds have been
available for other listing activities. In
FY 2007, we were able to use some of
the critical habitat subcap funds to fund
proposed listing determinations for
high-priority candidate species;
however, in FY 2008 we were unable to
do this because all of the critical habitat
subcap funds were needed to address
our workload for designating critical
habitat.
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12963
Thus, through the listing cap, the
critical habitat subcap, and the amount
of funds needed to address courtmandated critical habitat designations,
Congress and the courts have in effect
determined the amount of money
available for other listing activities.
Therefore, the funds in the listing cap,
other than those needed to address
court-mandated critical habitat for
already listed species, set the limits on
our determinations of preclusion and
expeditious progress.
Congress also recognized that the
availability of resources was the key
element in deciding whether, when
making a 12-month petition finding, we
would prepare and issue a listing
proposal or instead make a ‘‘warranted
but precluded’’ finding for a given
species. The Conference Report
accompanying Public Law 97–304,
which established the current statutory
deadlines and the warranted-butprecluded finding, states (in a
discussion on 90-day petition findings
that by its own terms also covers 12month findings) that the deadlines were
‘‘not intended to allow the Secretary to
delay commencing the rulemaking
process for any reason other than that
the existence of pending or imminent
proposals to list species subject to a
greater degree of threat would make
allocation of resources to such a petition
[that is, for a lower-ranking species]
unwise.’’
In FY 2008, expeditious progress is
that amount of work that could be
achieved with $8,206,940, which is the
amount of money that Congress
appropriated for the Listing Program
(that is, the portion of the Listing
Program funding not related to critical
habitat designations for species that are
already listed). Our process is to make
our determinations of preclusion on a
nationwide basis to ensure that the
species most in need of listing will be
addressed first and also because we
allocate our listing budget on a
nationwide basis. The $8,206,940 was
used to fund work in the following
categories: compliance with court orders
and court-approved settlement
agreements requiring that petition
findings or listing determinations be
completed by a specific date; section 4
(of the Act) listing actions with absolute
statutory deadlines; essential litigationrelated, administrative, and listing
program management functions; and
high-priority listing actions. The
allocations for each specific listing
action are identified in the Service’s FY
2008 Allocation Table (part of our
administrative record).
For FY 2009, on September 23, 2008
Congress passed a Continuing
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Resolution to operate the Federal
government at the FY 2008 level of
funding through March 6, 2009 (Pub. L.
110–329). Although we are currently
developing the allocations for specific
listing actions that we will fund during
FY 2009, we anticipate funding work to
comply with court orders and courtapproved settlement agreements, work
on statutorily required petition findings,
final listing determinations for those
species that were proposed for listing
with funds from FY 2008, and
continued work on proposed listing
determinations for high-priority species.
In FY 2007, we had more than 120
species with a listing priority number
(LPN) of 2, based on our September 21,
1983, guidance for assigning an LPN for
each candidate species (48 FR 43098).
Using this guidance, we assign each
candidate an LPN of 1 to 12, depending
on the magnitude of threats (high vs.
moderate to low), immediacy of threats
(imminent or nonimminent), and
taxonomic status of the species (in order
of priority: monotypic genus (a species
that is the sole member of a genus);
species; or part of a species (subspecies,
distinct population segment, or
significant portion of the range)). The
lower the listing priority number, the
higher the listing priority (that is, a
species with an LPN of 1 would have
the highest listing priority). Because of
the large number of high-priority
species, we further ranked the candidate
species with an LPN of 2 by using the
following extinction-risk type criteria:
International Union for the
Conservation of Nature and Natural
Resources (IUCN) Red list status/rank,
Heritage rank (provided by
NatureServe), Heritage threat rank
(provided by NatureServe), and species
currently with fewer than 50
individuals, or 4 or fewer populations.
Those species with the highest IUCN
rank (critically endangered), the highest
Heritage rank (G1), the highest Heritage
threat rank (substantial, imminent
threats), and currently with fewer than
50 individuals, or fewer than 4
populations, comprised a list of
approximately 40 candidate species
(‘‘Top 40’’). These 40 candidate species
have had the highest priority to receive
funding to work on a proposed listing
determination. As we work on proposed
listing rules for these 40 candidates, we
are applying the ranking criteria to the
next group of candidates with LPN of 2
and 3 to determine the next set of
highest priority candidate species.
To be more efficient in our listing
process, as we work on proposed rules
for these species in the next several
years, we are preparing multi-species
proposals when appropriate, and these
may include species with lower priority
if they overlap geographically or have
the same threats as a species with an
LPN of 2. In addition, available staff
resources are also a factor in
determining high-priority species
provided with funding. Finally,
proposed rules for reclassification of
threatened species to endangered are
lower priority, since as listed species,
they are already afforded the protection
of the Act and implementing
regulations.
We assigned the yellow-billed loon an
LPN of 8 based on moderate magnitude
and imminent threats. One or more of
the threats discussed above is occurring
throughout the range of the yellowbilled loon, either in its breeding or
wintering grounds, or during migration.
However, the primary threat to the
species that caused us to conclude
listing is warranted is subsistence
harvest, despite the species being closed
to hunting under the Migratory Bird
Treaty Act. Although subsistence
harvest is ongoing, the numbers taken
have varied substantially between years.
For the reasons discussed above,
although we believe subsistence harvest
is a substantial threat to the species, we
have concerns about the precision of the
numbers reported. In addition, if
changes in management are
implemented in the near future, we
believe there is time to reduce this
threat before it causes further
population-level impacts. While we
conclude that listing the yellow-billed
loon is warranted, an immediate
proposal to list this species is precluded
by other higher priority listing, which
we address below. Therefore, work on a
proposed listing determination for the
yellow-billed loon was, and will
continue to be in the next year,
precluded by work on higher priority
candidate species (i.e., species with LPN
of 2); listing actions with absolute
statutory, court ordered, or courtapproved deadlines; and final listing
determinations for those species that
were proposed for listing with funds
from FY 2008. This work includes all
the actions listed in the tables below
under expeditious progress.
As explained above, a determination
that listing is warranted but precluded
must also demonstrate that expeditious
progress is being made to add or remove
qualified species to and from the Lists
of Endangered and Threatened Wildlife
and Plants. (Although we do not discuss
it in detail here, we are also making
expeditious progress in removing
species from the list under the Recovery
program, which is funded by a separate
line item in the budget of the
Endangered Species Program. As
explained above in our description of
the statutory cap on Listing Program
funds, the Recovery Program funds and
actions supported by them cannot be
considered in determining expeditious
progress made in the Listing Program.)
As with our ‘‘precluded’’ finding,
expeditious progress in adding qualified
species to the Lists is a function of the
resources available and the competing
demands for those funds. Given that
limitation, we find that we made
expeditious progress in FY 2008 and are
making progress in FY 2009 in the
Listing Program. This progress included
preparing and publishing the following
determinations:
FY 2008 COMPLETED LISTING ACTIONS (SOME COMPLETED IN FY2009)
Title
Actions
10/09/2007 ....................
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90-Day Finding on a Petition to List
the
Black-Footed
Albatross
(Phoebastria nigripes) as Threatened or Endangered.
90-Day Finding on a Petition To List
the Giant Palouse Earthworm as
Threatened or Endangered.
90-Day Finding on a Petition To List
the Mountain Whitefish (Prosopium
williamsoni) in the Big Lost River,
ID, as Threatened or Endangered.
Notice of 90-day Petition Finding,
Substantial.
72 FR 57278–57283.
Notice of 90-day Petition Finding, Not
substantial.
72 FR 57273–57276.
Notice of 90-day Petition Finding, Not
substantial.
72 FR 59983–59989.
10/09/2007 ....................
10/23/2007 ....................
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FY 2008 COMPLETED LISTING ACTIONS (SOME COMPLETED IN FY2009)—Continued
Publication date
Title
Actions
10/23/2007 ....................
90-Day Finding on a Petition To List
the Summer-Run Kokanee Population in Issaquah Creek, WA, as
Threatened or Endangered.
Response to Court on Significant Portion of the Range, and Evaluation
of Distinct Population Segments,
for the Queen Charlotte Goshawk.
12-Month Finding on a Petition To
List the Jollyville Plateau salamander (Eurycea tonkawae) as Endangered With Critical Habitat.
90-Day Finding on a Petition To List
the Pygmy Rabbit (Brachylagus
idahoensis) as Threatened or Endangered.
90-Day Finding on Petition To List the
Amargosa River Population of the
Mojave Fringe-Toed Lizard (Uma
scoparia) as Threatened or Endangered With Critical Habitat.
12-Month Finding on a Petition To
List the Siskiyou Mountains Salamander (Plethodon stormi) and
Scott Bar Salamander (Plethodon
asupak) as Threatened or Endangered.
12-Month Finding on a Petition To
List the Gunnison’s Prairie Dog as
Threatened or Endangered.
12-Month Finding on a Petition To
List the Bonneville Cutthroat Trout
(Oncorhynchus clarki utah) as
Threatened or Endangered.
Listing Phyllostegia hispida (No Common
Name)
as
Endangered
Throughout Its Range.
Initiation of Status Review for the
Greater
Sage-Grouse
(Centrocercus urophasianus) as
Threatened or Endangered.
12-Month Finding on a Petition To
List the North American Wolverine
as Endangered or Threatened.
90-Day Finding on a Petition To List
the U.S. Population of Coaster
Brook Trout (Salvelinus fontinalis)
as Endangered.
90-Day Finding on a Petition To List
the
Western
Sage-Grouse
(Centrocercus
urophasianus
phaios) as Threatened or Endangered.
90-Day Finding on Petitions To List
the Mono Basin Area Population of
the
Greater
Sage-Grouse
(Centrocercus urophasianus) as
Threatened or Endangered.
Petition To List the San Francisco
Bay-Delta Population of the Longfin
Smelt (Spirinchus thaleichthys) as
Endangered.
90-Day Finding on a Petition to List
Kokanee (Oncorhynchus nerka) in
Lake Sammamish, Washington, as
Threatened or Endangered.
12-Month Finding on a Petition To
List the White-tailed Prairie Dog
(Cynomys leucurus) as Threatened
or Endangered.
Notice of 90-day Petition Finding, Not
substantial.
72 FR 59979–59983.
Response to Court .............................
72 FR 63123–63140.
Notice of 12-month Petition Finding,
Warranted but Precluded.
72 FR 71039–71054.
Notice of 90-day Petition Finding,
Substantial.
73 FR 1312–1313.
Notice of 90-day Petition Finding,
Substantial.
73 FR 1855–1861.
Notice of 12-month Petition Finding,
Not Warranted.
73 FR 4379–4418.
Notice of 12-month Petition Finding,
Warranted.
73 FR 6660–6684.
Notice of Review ................................
73 FR 7236–7237.
Proposed Listing, Endangered ...........
73 FR 9078–9085.
Notice of Status Review .....................
73 FR 10218–10219.
Notice of 12-month petition finding,
Not warranted.
73 FR 12929–12941.
Notice of 90-day Petition Finding,
Substantial.
73 FR 14950–14955.
Notice of 90-day Petition Finding,
Substantial.
73 FR 23170–23172.
Notice of 90-day Petition Finding,
Substantial.
73 FR 23173–23175.
Notice of 90-day Petition Finding,
Substantial.
73 FR 24611–24915.
Notice of 90-day Petition Finding,
Substantial.
73 FR 24915–24922.
Notice of Status Review .....................
73 FR 24910–24911.
11/08/2007 ....................
12/13/2007 ....................
1/08/2008 ......................
1/10/2008 ......................
1/24/2008 ......................
2/05/2008 ......................
02/07/2008 ....................
02/19/2008 ....................
02/26/2008 ....................
03/11/2008 ....................
03/20/2008 ....................
04/29/2008 ....................
04/29/2008 ....................
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05/06/2008 ....................
05/06/2008 ....................
05/06/2008 ....................
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FY 2008 COMPLETED LISTING ACTIONS (SOME COMPLETED IN FY2009)—Continued
Publication date
Title
Actions
05/15/2008 ....................
90-Day Finding on a Petition To List
the
Ashy
Storm-Petrel
(Oceanodroma
homochroa)
as
Threatened or Endangered.
Determination of Threatened Status
for
the
Polar
Bear
(Ursus
maritimus) Throughout Its Range;
Final Rule.
Special Rule for the Polar Bear; Interim Final Rule.
Initiation of Status Review for the
Northern Mexican Gartersnake
(Thamnophis eques megalops).
90-Day Finding on a Petition To List
the Long-Tailed Duck (Clangula
hyemalis) as Endangered.
90-Day Finding on a Petition To Reclassify
the
Delta
Smelt
(Hypomesus transpacificus) From
Threatened to Endangered.
90-Day Finding on a Petition To List
the Tucson Shovel-Nosed Snake
(Chionactis occipitalis klauberi) as
Threatened or Endangered with
Critical Habitat.
Proposed Endangered Status for Reticulated Flatwoods Salamander;
Proposed Designation of Critical
Habitat for Frosted Flatwoods Salamander and Reticulated Flatwoods
Salamander.
12-month Finding on a Petition To
List the Bonneville Cutthroat Trout
as Threatened or Endangered.
90-Day Finding on a Petition To List
the Least Chub.
Listing 48 Species on Kauai as Endangered and Designating Critical
Habitat.
90-Day Finding on a Petition To List
the Sacramento Valley Tiger Beetle
as Endangered.
90-Day Finding on a Petition To List
the Dusky Tree Vole (Arborimus
longicaudus silvicola) as Threatened or Endangered.
12-Month Finding on a Petition To
List
the
Northern
Mexican
Gartersnake (Thamnophis eques
megalops) as Threatened or Endangered With Critical Habitat; Proposed Rule.
90-Day Finding on a Petition To List
the Black-tailed Prairie Dog as
Threatened or Endangered.
90-Day Finding on a Petition To List
the
Sacramento
Mountains
Checkerspot Butterfly (Euphydryas
anicia cloudcrofti) as Endangered
with Critical Habitat.
90-Day Finding on a Petition to
Change the Listing Status of the
Canada Lynx.
Partial 90-Day Finding on a Petition
To List 475 Species in the Southwestern United States as Threatened or Endangered With Critical
Habitat.
Notice of 90-day Petition Finding,
Substantial.
73 FR 28080–28084.
Final Listing, Threatened ....................
73 FR 28211–28303.
Interim Final Special Rule ..................
73 FR 28305–28318.
Notice of Status Review .....................
73 FR 30596–30598.
Notice of 90-day Petition Finding, Not
substantial.
73 FR 34686–34692.
Notice of 90-day Petition Finding,
Substantial.
73 FR 39639–39643.
Notice of 90-day Petition Finding,
Substantial.
73 FR 43905–43910.
Proposed Critical Habitat, Proposed
Listing, Endangered.
73 FR 47257–47324.
Notice of 12-month petition finding,
Not warranted.
73 FR 52235–52256.
Notice of 90-day Petition Finding,
Substantial.
Proposed Listing, Endangered; Proposed Critical Habitat.
73 FR 61007–61015.
Notice of 90-day Petition Finding, Not
substantial.
73 FR 63421–63424.
Notice of 90-day Petition Finding,
Substantial.
73 FR 63919–63926.
Notice of 12-month petition finding,
Warranted but precluded.
73 FR 71787–71826.
Notice 90-day Petition Finding, Substantial.
73 FR 73211–73219.
Notice 90-day Petition Finding, Substantial.
73 FR 74123–74129.
Notice 90-day Petition Finding, Substantial.
73 FR 76990–76994.
Notice 90-day Petition Finding, Not
substantial.
74 FR 419–427.
05/15/2008 ....................
05/15/2008 ....................
05/28/2008 ....................
06/18/2008 ....................
07/10/2008 ....................
07/29/2008 ....................
8/13/2008 ......................
9/9/2008 ........................
10/15/2008 ....................
10/21/2008 ....................
10/24/2008 ....................
10/28/2008 ....................
11/25/2008 ....................
12/02/2008 ....................
12/05/2008 ....................
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12/18/2008 ....................
1/06/2009 ......................
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73 FR 62591–62742.
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12967
FY 2008 COMPLETED LISTING ACTIONS (SOME COMPLETED IN FY2009)—Continued
Publication date
Title
Actions
2/05/2009 ......................
Partial 90-Day Finding on a Petition
To List 206 Species in the Midwest
and Western United States as
Threatened or Endangered With
Critical Habitat.
Notice 90-day Petition Finding, Not
substantial.
Our expeditious progress also
included work on listing actions, which
were funded in FY 2008, but have not
yet been completed to date. These
actions are listed below. Actions in the
top section of the table are being
conducted to meet deadlines set by a
court. Actions in the middle section of
the table are being conducted to meet
statutory timelines, that is, timelines
required under the Act. Actions in the
bottom section of the table are high
priority listing actions. These actions
include work primarily on species with
an LPN of 2, and selection of these
species is partially based on available
staff resources, and when appropriate,
include species with a lower priority if
FR pages
74 FR 6122–6128.
they overlap geographically or have the
same threats as the species with the
high priority. Including these species
together in the same proposed rule
results in considerable savings in time
and funding, as compared to preparing
separate proposed rules for each of them
in the future.
ACTIONS FUNDED IN FY 2008 BUT NOT YET COMPLETED
Species
Action
Actions With Court Order/Settlement Agreement Deadlines
SW Bald Eagle DPS .................................................................................
Greater and Western Sage Grouse .........................................................
12-month petition finding.
12-month petition finding.
Actions With Statutory Deadlines
Phyllostegia hispida ..................................................................................
Black-footed albatross ..............................................................................
Mount Charleston blue butterfly ...............................................................
Goose Creek milk-vetch ...........................................................................
Mojave fringe-toed lizard ..........................................................................
White-tailed prairie dog ............................................................................
Pygmy rabbit (rangewide) ........................................................................
Wyoming pocket gopher ...........................................................................
Llanero coqui ............................................................................................
American pika ...........................................................................................
206 species (partially completed) .............................................................
475 Southwestern species (partially completed) .....................................
Final listing.
12-month petition finding.
12-month petition finding.
12-month petition finding.
12-month petition finding.
12-month petition finding.
12-month petition finding.
90-day petition finding.
90-day petition finding.
90-day petition finding.
90-day petition finding.
90-day petition finding.
PWALKER on PROD1PC71 with PROPOSALS2
High Priority Listing Actions
21 Oahu candidate species (16 plants, 5 damselflies) (18 with LPN =2,
3 with LPN = 3, 1 with LPN =9).
3 southeast aquatic species (Georgia pigtoe, interrupted rocksnail,
rough hornsnail) 1 (all with LPN = 2).
Casey’s june beetle (LPN = 2) .................................................................
Sand dune lizard (LPN = 2) .....................................................................
2 southwest springsnails (Pyrgulopsis bernadina (LPN = 2),
Pyrgulopsis trivialis (LPN = 2)).
3 southwest springsnails (Pyrgulopsis chupaderae (LPN = 2),
Pyrgulopsis gilae (LPN = 11), Pyrgulopsis thermalis (LPN = 11)).
2 mussels (rayed bean (LPN = 2), snuffbox No LPN) .............................
2 mussels (sheepnose (LPN = 2), spectaclecase (LPN = 4),) ................
Ozark hellbender 2 (LPN = 3) ...................................................................
Altamaha spinymussel (LPN = 2) .............................................................
5 southeast fish (rush darter (LPN = 2), chucky madtom (LPN = 2),
yellowcheek darter (LPN = 2), Cumberland darter (LPN = 5), laurel
dace (LPN = 5)).
3 Colorado plants (Pagosa skyrocket (Ipomopsis polyantha) (LPN = 2),
Parchute beardtongue (Penstemon debilis) (LPN = 2), Debeque
phacelia (Phacelia submutica) (LPN = 8)).
Proposed listing.
Proposed listing.
Proposed listing.
Proposed listing.
Proposed listing.
Proposed listing.
Proposed
Proposed
Proposed
Proposed
Proposed
listing.
listing.
listing.
listing.
listing.
Proposed listing.
1 Funds
for listing actions for 3 of these species were also provided in FY 2007.
funded a proposed rule for this subspecies with an LPN of 3 ahead of other species with LPN of 2, because the threats to the species
were so imminent and of a high magnitude that we considered emergency listing if we were unable to fund work on a proposed listing rule in FY
2008.
2 We
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We have endeavored to make our
listing actions as efficient and timely as
possible, given the requirements of the
relevant law and regulations, and
constraints relating to workload and
personnel. We are continually
considering ways to streamline
processes or achieve economies of scale,
such as by batching related actions
together. Given our limited budget for
implementing section 4 of the Act, these
actions described above collectively
constitute expeditious progress.
The yellow-billed loon will be added
to the list of candidate species upon
publication of this 12-month finding.
We will continue to monitor the status
of this species as new information
becomes available, and information on
the species’ distribution, status, and
threats will be evaluated every year. In
particular, we will work with the
AMBCC and the State of Alaska to
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improve the reliability of subsistence
harvest data, and to substantially
increase education and law enforcement
efforts to reduce levels of these threats.
This review will determine if the
species should be removed or
maintained as a candidate species, or if
a change in status is warranted,
including the need to make prompt use
of emergency listing procedures.
We intend that any proposed listing
action for the yellow-billed loon will be
as accurate as possible. Therefore, we
will continue to accept additional
information and comments from all
concerned governmental agencies, the
scientific community, industry, or any
other interested party concerning this
finding.
References Cited
A list of the references used to
develop this proposed rule is available
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upon request (see FOR FURTHER
INFORMATION CONTACT).
Author
The primary authors of this 12-month
finding are the staff members of the
Fairbanks Fish and Wildlife Field Office
(see FOR FURTHER INFORMATION CONTACT).
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: March 12, 2009.
Rowan W. Gould,
Acting Director, Fish and Wildlife Service.
[FR Doc. E9–6012 Filed 3–24–09; 8:45 am]
BILLING CODE 4310–55–P
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Agencies
[Federal Register Volume 74, Number 56 (Wednesday, March 25, 2009)]
[Proposed Rules]
[Pages 12932-12968]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E9-6012]
[[Page 12931]]
-----------------------------------------------------------------------
Part II
Department of the Interior
-----------------------------------------------------------------------
Fish and Wildlife Service
50 CFR Part 17
Endangered and Threatened Wildlife and Plants; 12-Month Finding on a
Petition To List the Yellow-Billed Loon as Threatened or Endangered;
Proposed Rules
Federal Register / Vol. 74, No. 56 / Wednesday, March 25, 2009 /
Proposed Rules
[[Page 12932]]
-----------------------------------------------------------------------
DEPARTMENT OF THE INTERIOR
Fish and Wildlife Service
50 CFR Part 17
[FWS-R7-ES-2009-0133; MO9221050083-B2]
Endangered and Threatened Wildlife and Plants; 12-Month Finding
on a Petition To List the Yellow-Billed Loon 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 yellow-billed loon (Gavia
adamsii) as threatened or endangered, with critical habitat, under the
Endangered Species Act of 1973, as amended (Act). The petitioners
provided two listing options for consideration by the Service: (1)
Listing the yellow-billed loon throughout its range, or (2) listing the
United States population of the yellow-billed loon as a Distinct
Population Segment (DPS). After a review of the best available
scientific and commercial information, we have determined that listing
the yellow-billed loon rangewide under the Act is warranted but
precluded by other higher priority listing actions.
DATES: This finding was made on March 25, 2009.
ADDRESSES: This finding is available on the Internet at https://www.regulations.gov. Data, information, comments, or questions
regarding this notice should be submitted to the Field Supervisor,
Endangered Species Branch, Fairbanks Fish and Wildlife Field Office,
U.S. Fish and Wildlife Service, 101-12th Ave., Room 110, Fairbanks, AK
99701. The complete administrative file for this finding is available
for public inspection, by appointment, during normal business hours at
the above address.
FOR FURTHER INFORMATION CONTACT: Mr. Ted Swem, Fairbanks Fish and
Wildlife Field Office (see ADDRESSES) (telephone 907-456-0441;
facsimile 907-456-0208). If you use a telecommunications device for the
deaf (TDD), call the Federal Information Relay Service (FIRS) at 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 presenting substantial scientific and commercial
information that listing may be warranted, we make a finding within 12
months of the date of receipt of the petition on whether the petitioned
action is: (a) Not warranted, (b) warranted, or (c) warranted, but that
immediate proposal of a regulation implementing the petitioned action
is precluded by other pending proposals to determine whether species
are 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. 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 is, therefore, subject to a new finding to be made within
12 months and subsequently thereafter until we take action on a
proposal to list or withdraw our original finding. We must publish
these 12-month findings in the Federal Register.
Previous Federal Actions
On April 5, 2004, we received a petition from the Center for
Biological Diversity (CBD) (Sitka, AK), Natural Resources Defense
Council (Washington, DC), Pacific Environment (San Francisco, CA),
Trustees for Alaska (Anchorage, AK), Kaira Club (Chukotka, Anadyr,
Russia), Kronotsky Nature Preserve (Kamchatka Region, Russia), Taiga
Rangers (Khabarovsk Region, Russia), Yuzhno-Sakhalinsk Local Public
Fund (Sakhalin Region, Russia), Interregional Public Charitable
Organization of Far Eastern Resource Centers (Vladivostok, Russia),
Kamchatka Branch of Pacific Institute of Geography (Petropavlovsk-
Kamchatsky, Russia), and Kamchatka League of Independent Experts
(Petropavlovsk-Kamchatsky, Russia) to list the yellow-billed loon as
endangered or threatened throughout its range, or as a Distinct
Population Segment in the United States, and to designate critical
habitat once listed. The petition summarizes threats to the species
based on CBD's review of Fair's (2002) report, prepared for the Natural
Resources Defense Council and Trustees for Alaska, on the status and
significance of the species in Alaska, as well as CBD's review of the
scientific literature. In September 2006, the Service completed a
``Conservation Agreement for the Yellow-billed Loon (Gavia adamsii)''
with Federal, State, and local partners. In response to the petition,
we published a 90-day finding on the yellow-billed loon in the Federal
Register on June 6, 2007 (72 FR 31256). In the 90-day finding we
determined that the petition presented substantial scientific or
commercial information to indicate that a listing may be warranted and
announced that a status review would be promptly commenced. In that
notice we announced the opening of a 60-day information collection
period and invited the public to submit to us any pertinent information
concerning the status of or threats to this species. Approximately
28,000 comments were received during the information collection period.
We also consulted with recognized yellow-billed loon experts and other
Federal and State agencies. We sent letters to national wildlife or
natural resource agencies in Canada, China, Japan, North Korea, Norway,
Republic of Korea (South Korea), and the Russian Federation, asking for
information about ongoing management measures and any conservation and
management strategies being developed to protect the species. We
received a formal response from the government of Canada, and an
informal response from a government biologist in the Russian
Federation.
On June 11, 2007, we received a 60-day notice of intent to sue from
the Center for Biological Diversity alleging a violation of section 4
of the ESA for failure to complete a 12-month finding on the petition.
We informed the plaintiffs by letter dated July 9, 2007, that further
action on the petition was precluded by higher priority listing actions
but that, pending the fiscal year 2008 allocation of funds, we hoped to
complete the 12-month finding within that fiscal year.
On December 19, 2007, the Center for Biological Diversity (CBD)
filed a complaint alleging that the Service had failed to make a timely
12-month finding on the petition, as required under section 4 of the
ESA. Consistent with a settlement agreement reached between the Service
and CBD, the Court ordered the Service to submit this 12-month finding
for publication to the Federal Register by February 15, 2009. Because
the Service later received substantial new information to be evaluated
and considered in the 12-month finding, we subsequently sought and were
granted a one month extension with a new deadline of March 16, 2009.
This notice constitutes a 12-month finding for the petition to list
the yellow-billed loon as threatened or endangered. The petitioners
provided two listing options for consideration by the Service: (1)
Listing the yellow-billed loon throughout its range, or (2) listing the
United States population of the yellow-billed loon as a Distinct
Population Segment (DPS). Because we find that listing the yellow-
billed loon rangewide is warranted at this time,
[[Page 12933]]
there is no need to conduct further analysis of whether listing the
United States population of the yellow-billed loon as a DPS, which is a
smaller geographic entity than the entire range, is warranted, as this
consideration is subsumed by the rangewide warranted but precluded
finding.
Outline of This Notice
In this notice, we first provide background information on the
biology of the yellow-billed loon. Next, we address each of the
categories of factors listed in section 4(a)(1) of the Act. For each
factor, we first determine whether any stressors, or risk factors,
appear to be negatively affecting yellow-billed loons anywhere within
the species' range. If we determine they are, then we evaluate whether
each of these risk factors is resulting in population-level effects
that are significant to the determination of the conservation status of
the species. If so, we describe it as a ``threat.'' The fact that we
find a stressor to be a threat to the species does not necessarily mean
that the species meets the definition of threatened or endangered.
Rather, in the subsequent finding section, we then consider each of the
stressors and identified threats, individually and cumulatively, and
make a determination with respect to whether the species is endangered
or threatened according to the statutory standard.
The term ``threatened species'' means any species (or subspecies
or, for vertebrates, distinct population segments) that is likely to
become an endangered species within the foreseeable future throughout
all or a significant portion of its range. The Act does not define the
term ``foreseeable future.'' However, in a January 16, 2009, memorandum
addressed to the Acting Director of the U.S. Fish and Wildlife Service,
the Office of the Solicitor, Department of the Interior, concluded, ``*
* * as used in the ESA, Congress intended the term `foreseeable future'
to describe the extent to which the Secretary can reasonably rely on
predictions about the future in making determinations about the future
conservation status of the species.'' In a footnote, the memorandum
states, ``In this memorandum, references to `reliable predictions' are
not meant to refer to reliability in a statistical sense. Rather, I use
the words ``rely'' and ``reliable'' according to their common, non-
technical meanings in ordinary usage. Thus, for the purposes of this
memorandum, a prediction is reliable if it is reasonable to depend upon
it in making decisions'' (M-37021, January 16, 2009).
Species Biology
The yellow-billed loon is a migratory bird. Solitary pairs breed on
lakes in the arctic tundra of the United States, Russia, and Canada
from June to September. During the remainder of the year the species
winters in more southern coastal waters of the Pacific Ocean and the
Norway and North Seas. Non-breeding birds remain in marine waters
throughout the year, either in wintering areas or offshore from
breeding grounds.
The following information regarding the description and natural
history of the yellow-billed loon (American Ornithologists' Union 1998,
p. 5) has been condensed from the status assessments conducted by North
(1994) and Earnst (2004), and updated with information that has become
available since then.
Taxonomy and Description
The yellow-billed loon (Order Gaviiformes, Family Gaviidae) is one
of the largest of the five loon species and similar in appearance to
the common loon (Gavia immer). There are no recognized subspecies or
geographic variations (American Ornithologists' Union 1998, p. 5). A
field characteristic that distinguishes yellow-billed loons from common
loons is their larger yellow or ivory-colored bill. Adults weigh 4,000
to 6,000 grams (8.8 to 13.2 pounds) and are 774 to 920 millimeters (30
to 37 inches) in length. Breeding (alternate) plumage of adults of both
sexes is black on top with white spots on the wings and underside, and
white stripes on the neck. Non-breeding (basic) plumage is gray-brown
with fewer and less distinct white spots than breeding plumage, with
paler undersides and head, and a blue-gray bill. Hatchlings have dark
brown and gray down, and juveniles are gray with a paler head (North
1994, p. 2). Yellow-billed loons are specialized for aquatic foraging
with a streamlined shape and legs near the rear of the body, and are
unable to take flight from land.
Feeding Habits
Yellow-billed loons forage underwater for fish and aquatic
invertebrates. Limited information exists on specific prey species
consumed. Marine prey species collected from loons wintering in
southeast Alaska and Canada include fish such as sculpins (Leptocottus
armatus, Myoxocephalus sp.), Pacific tomcod (Microgadus proximus), and
rock cod (Sebastodes sp.), and invertebrates such as amphipods
(Orchomonella sp., Anonyx nirgax), isopods (Idothea sp.), shrimps
(Pandalus danae, Spirontocaris ochotensis), hermit crabs (Pagarus sp.),
and marine worms (Nereis sp.) (Bailey 1922, p. 205; Cottam and Knappen
1939, p. 139; North 1994, pp. 6-7; Earnst 2004, pp. 9-10). Pacific sand
dabs (Citharichthys sordidus) were found in a yellow-billed loon
collected extralimitally (i.e., outside the limits of the species'
range) in Baja California (Jehl 1970, p. 376) and sculpin
(Myoxocephalus scorpius) in a specimen collected in Norway (Collett
1894, p. 280). Prey species taken in other wintering grounds, such as
in the Yellow Sea (which supports 276 fish species and 54 crustacean
species; UNDP 2002, p. 8) are unknown.
During the breeding season, foraging habitats include lakes,
rivers, and the nearshore marine environment. Successfully breeding
adults feed their young almost entirely from the brood-rearing lake
(North 1994, p. 14). Ninespine sticklebacks (Pungitius pungitius) and
least cisco (Coregonus sardinella) are thought to be the main foods of
chicks in Alaska (Earnst 2004, p. 9). Other freshwater prey available
in Alaska that are likely utilized include Alaska blackfish (Dallia
pectoralis), fourhorn sculpins (M. quadricornus), amphipods, and
isopods (Earnst 2004, p. 9), as well as aquatic plant material
(Sj[ouml]lander and [Aring]gren 1976, p. 460). In arctic Russia,
limited stomach content analysis indicates sticklebacks, salmon,
crustaceans, beetles, and plant vegetation are consumed during the
breeding season (Uspenskii 1969, p. 130).
Breeding Habitat and Territories
Yellow-billed loons nest exclusively on margins of lakes in coastal
and inland low-lying tundra from 62[deg] to 74[deg] North (N) latitude.
Lakes that support breeding loons have abundant fish populations.
Studies of yellow-billed loon habitat have identified several
characteristics that predict loon presence. These may be indirect
measures or correlates of the actual characteristics necessary or
preferred by loons, such as fish availability. Predictors of yellow-
billed loon presence on a lake include water depths greater than 2
meters (m) or 6.5 feet (ft) allowing for unfrozen water under the ice
during winter; large lake areas (at least 13.4 hectares (ha) or 33
acres (ac)); connections to streams that may supply fish; highly
convoluted, vegetated, and low-lying shorelines; clear water; and
dependable water levels (Earnst et al. 2006, pp. 230-233; Stehn et al.
2005, pp. 9-10; North 1994, p. 6). Probability of yellow-billed loon
presence on a lake increases with the absence of Pacific
[[Page 12934]]
loons (Gavia pacifica) (Earnst et al. 2006, p. 233; Stehn et al. 2005,
p. 9). Breeding lakes may be near major rivers, but are usually not
connected to them, possibly because greater fluctuations associated
with river connections may flood nests or cause turbidity that
compromises foraging success (North & Ryan 1989, p. 303). Falling water
levels may also expose loon nests to increased risk of predation
(Kertell 1996, p. 356).
Breeding territories (areas defended against other yellow-billed
loons and other loon species, particularly Pacific loons) may include
one or more lakes or parts of lakes. Territory size, likely dependent
upon lake size and quality, ranged from 13.8 to greater than 100 ha (34
to greater than 247 ac) on the Colville River Delta, Alaska (North
1986, as cited in North 1994, p. 10). It is thought that individual
loons occupy the same breeding territory throughout their reproductive
life. Some breeding lakes are ``known to be reoccupied over long time
spans'' (North 1994, p. 10), most likely by the same monogamous pair
(North 1994, p. 10), similar to common loons (Evers 2004, p. 13).
Nesting Sites and Behavior
Nest sites are usually located on islands, hummocks, or peninsulas,
along low shorelines, within 1 m (3 ft) of water. The nest location,
which may be used in multiple years, usually provides a better view of
the surrounding land and water than other available lakeshore
locations. Nests are constructed of mud or peat, and are often lined
with vegetation. One or two large, smooth, mottled brown eggs are laid
in mid-to late June (North 1994, pp. 11-12). Egg replacement after nest
predation occurs rarely; unless failure occurs very early in the
season, the short arctic summer probably precludes the production or
success of replacement clutches (Earnst 2004, p. 8). Hatching occurs
after 27 to 28 days of incubation by both sexes. Although the age at
which young are capable of flight is unknown, it is probably similar to
common loons (8-9, possibly up to 11, weeks). The young leave the nest
soon after hatching, and the family may move between natal and brood-
rearing lakes. Both males and females participate in feeding and caring
for young (North 1994, p. 13).
Life History
There is no reliable scientific information on lifespan and
survivorship, but as large-bodied birds with low clutch size, yellow-
billed loons are probably K-selected (long-lived and dependent upon
high annual adult survival to maintain populations). On average,
individuals reach sexual maturity at 3 years of age, but may not
acquire breeding territories until at least 4 years of age (North 1994,
p. 15). The average age at first breeding for common loons is 6 years
(Evers 2004, p. 18).
Territory occupancy and nesting success of yellow-billed loons were
studied on the Colville River Delta during 18 years between 1983 and
2007. Ground-based surveys in 1983 and 1984 found 76 and 79 percent of
the territorial pairs nesting, respectively (Field et al. 1993, p.
329). The same territories studied in 1983 and 1984 were visited in
1989 and 1990, and 42 percent and 67-71 percent, respectively, of the
territorial pairs were found nesting (Field et al. 1993, p. 329; North
1993, p. 46). Low nest occupancy recorded in 1989 may have been a
result of surveys being conducted late in incubation (July 9-16, 1989)
after nests of some pairs had already failed; weekly monitoring surveys
of nesting yellow-billed loons on the Colville River Delta in 2005-2007
found that 19-36 percent of the nests had failed by July 10-12 of those
years (Johnson et al. 2006, Table 5; Johnson et al. 2007, Table 5;
Johnson et al. 2008, Table 4). However, low nest occupancy occurred in
some years during two long-term studies of yellow-billed loons on the
Colville Delta. The percentage of territorial pairs nesting ranged from
39 percent to 89 percent during a 6-year ground-based study (1995-2000;
Earnst 2004, p. 9) and from 43 percent to 76 percent (average of 58
percent) during 13-years of aerial surveys (1993-2007; ABR, Inc. 2007,
Table 1; ABR, Inc., unpublished data).
Reproductive success, like nest occupancy by territorial pairs,
varied on the Colville River Delta. Low reproductive success has been
attributed to late ice melt or extreme flooding (Earnst 2004, p. 9).
Based on Mayfield survival rates (a technique for measuring nesting
success in which the number of days from discovery of the nest to
fledging or failure (exposure days) is used to compute a daily nest-
survival rate) calculated for yellow-billed loons nesting on the
Colville River Delta in 1995-2000, 4 percent to 60 percent of eggs/
chicks survived from laying to age 6 weeks (Earnst 2004, p. 9).
Apparent nesting success [(broods/nests) x 100] based on broods counted
on aerial surveys conducted 8 weeks apart during nesting and brood-
rearing ranged from 19 percent to 64 percent annually in 13 years
between 1993 and 2007 (ABR, Inc. 2007, Table 1; ABR, Inc., unpublished
data). During the last three years (2005-2007) of this study, weekly
monitoring surveys were conducted after nests were found. Apparent
nesting success calculated from these weekly surveys was 1-10 percent
higher than calculations based on nesting and brood-rearing surveys
conducted 8 weeks apart, because the more frequent surveys identified
nests with chicks that did not survive to 5-6 weeks of age (Johnson et
al. 2006, p. 17; Johnson et al. 2007, p. 16; Johnson et al. 2008, p.
15). The highest recorded apparent nesting success on the Colville
River Delta was 71 percent in 2007 based on weekly monitoring surveys
(Johnson et al. 2008, p. 15).
Breeding Distribution
Yellow-billed loons nest near freshwater lakes in arctic tundra of
Alaska on the Arctic Coastal Plain (ACP), northwestern Alaska, and St.
Lawrence Island; in Canada east of the Mackenzie Delta and west of
Hudson Bay; and in Russia on a relatively narrow strip of coastal
tundra from the Chukotka Peninsula in the east and on the western
Taymyr Peninsula in the west, with a break in distribution between
these two areas (Earnst 2004, p. 3; North 1993, p. 42; Red Data Book of
the Russian Federation 2001, p. 366; Ryabitsev 2001, p. 22; Il'ichev
and Flint 1982, p. 277; Pearce et al. 1998, p. 369). Loons are sparsely
distributed across their range, although, perhaps because of non-
uniform quality of habitat, at a large scale breeding birds are
somewhat clumped in distribution.
Breeding Bird Densities
Most of the breeding range of the yellow-billed loon has not been
adequately surveyed, and only in Alaska have surveys been conducted
specifically for breeding yellow-billed loons. Unless otherwise noted,
the following discussion includes data from waterfowl surveys for which
loons were not focal species. In these surveys, density estimates were
not corrected for visibility bias and so are minimal estimates (see
discussion in Groves et al. 1996, pp. 193-194). Surveys enumerate all
yellow-billed loons seen on breeding grounds, including an unknown
proportion of which are non-breeders (Earnst et al. 2005, p. 300).
Alaska
Based on fixed-wing aerial survey data (1992 to 2003 ACP and North
Slope Eider (NSE) surveys conducted by the Service), Earnst et al.
(2005, p. 300) calculated that most of the population on the ACP of
Alaska occurred within concentration areas with more than 0.11
individuals per square kilometer (km2). Such areas comprised
only 12 percent of the surveyed area yet contained 53 percent of
yellow-billed loon sightings.
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The largest concentration area was between the Meade and Ikpikpuk
Rivers; it covered only 8 percent of the survey area, but had 38
percent of yellow-billed loon sightings (Earnst et al. 2005, p. 300).
Other notable concentrations were on the Colville River Delta and west,
southwest, and east of Teshekpuk Lake (Earnst et al. 2005, p. 300). In
aerial lake-circling surveys designed for yellow-billed loons (fixed-
wing aircraft were used 1992-2000; helicopters were used 2001-2007),
the average density on the Colville River Delta (363 km2
(140 mi2) survey area) was 0.13 individuals per
km2 during 10 years from 1993 to 2004 (Johnson et al. 2005,
p. 65), and 0.15 to 0.17 individuals per km2 from 2005 to
2007 (Johnson et al. 2006, p. 15; Johnson et al. 2007, p. 16; Johnson
et al. 2008, p. 15). Similar surveys for yellow-billed loons in a
larger area (878 km2) (339 mi2) in the Northeast
Planning Area (NE) of the National Petroleum Reserve-Alaska (NPR-A) in
2001-2004 indicated densities there were lower (0.07 individuals/
km2; Johnson et al. 2005, p. 68), except that the density in
an area adjacent to Fish and Judy Creeks was similar to that of the
Colville River Delta (Johnson et al. 2005, p. 68; Johnson et al. 2006,
p. 15; Johnson et al. 2007, p. 16). In western Alaska, where fixed-wing
aerial surveys were also designed specifically for loons, density on
the northern Seward Peninsula averaged 0.058 (standard error
(SE)=0.011; standard error is a measure of the variability in the data)
individuals/km2 over 2 years (Bollinger et al. 2008, p. 5).
Canada
In Canada, concentrations are found on parts of Victoria and Banks
Islands, on the mainland, the Kent Peninsula, east of Bathhurst Inlet
and west of Ellice River, the west side of Boothia Peninsula, and the
lake district between Great Slave Lake and Baker Lake, including the
Thelon Game Sanctuary (North 1993, p. 42). Densities obtained in 2005
and 2007 from fixed-winged aerial waterfowl surveys on southern
Victoria Island and the Kent Peninsula ranged from 0.017 to 0.16 birds/
km2 (Conant et al. 2006, pp. 2, 7; Groves in litt. 2008);
lower densities (0.004-0.027 birds/km2) were found in
surveys on the Queen Maud Gulf Migratory Bird Sanctuary, King William
Island, Rasmussen Lowlands, and Kugluktuk (Conant et al. 2007, pp. 10,
12; Groves in litt. 2008). On western Victoria Island, Raven and
Dickson (2006, p. 24) estimated densities from 0.004 to 0.08 birds/
km2 from helicopter-based waterfowl surveys. Hines (in litt.
2008) estimated 0.01 yellow-billed loons/km2 on Banks Island
from helicopter-based waterfowl surveys in 1992 and 1993.
Russia
In Russia, breeding concentrations have been identified on the
Chukotka (Chukotskiy) Peninsula (Il'ichev and Flint 1982, p. 280;
Solovyov 1992, p. 21), Kyttyk Peninsula and Ayon Island in western
Chukotka (Solovyova 2007, p. 6), and the western Taymyr Peninsula
(Krechmar 1966, p. 200; Il'ichev and Flint 1982, p. 277). Hodges and
Eldridge (2001, pp. 141-142), using fixed-winged aircraft in the only
aerial waterfowl survey of the eastern Siberian coast, found
concentrations of approximately 0.01 birds/km2 on the Cape
Schmidt coast of the Chukotka Peninsula, between the Indigirka and Yana
River Deltas, and between the Indigirka and Kolyma Deltas. Post-
breeding density on Kyttyk Peninsula in western Chukotka was
approximately 0.52 birds/km2 (including young birds) during
late July-August 2003-2007 (calculated from ground surveys, Solovyova
2007, p. 6). No density estimates are available for the Taymyr
Peninsula.
Nest Densities
Nest density on 363 km2 (140 mi2) of the
Colville River Delta, Alaska, ranged from 0.03 to 0.08 nests/
km2 during 13 years of aerial surveys for yellow-billed
loons during 1993-2007 (Johnson et al. 1999, p. 44; Burgess et al.
2003, p. 36; Johnson et al. 2003, p. 43; Johnson et al. 2004, p. 74;
Johnson et al. 2005, p. 64; Johnson et al. 2006, p. 15; Johnson et al.
2007, p. 16; Johnson et al. 2008, p. 15). Nest density in an 878
km2 (339 mi2) survey area of NE NPR-A was 0.03
nests/km2 in each year during 2002-2004. Higher densities
within this area were found along Fish and Judy Creeks (helicopter-
based surveys; Johnson et al. 2005, p. 68). In Russia, Solovyov (1992)
reported 0.18 nests/km2 on a 27.6 km2 (10.6
mi2) plot searched from the ground on Belyaka Spit near
Kolyuchin Bay on the Chukotka Peninsula. On the Kyttyk Peninsula in
western Chukotka, yellow-billed loons nest on approximately 25 percent
of lakes larger than 4 ha (9.9 acres) (Solovyova 2007, p. 6).
Foraging Distribution During Breeding Season
Yellow-billed loons use nearshore and offshore marine waters
adjacent to their breeding areas for foraging in summer. Such habitats
are likely used by both breeding adults and younger or non-territorial
birds (Earnst 2004, p. 7). Earnst (2004, pp. 6-7) reviewed yellow-
billed loon distribution information from fixed-wing aerial waterfowl
surveys that Fischer et al. (2002) conducted in 1999 and 2000 off the
coasts of Canada's arctic islands and the ACP of Alaska between Cape
Halkett and Brownlow Point. Similar surveys conducted between Barrow
and Demarcation Point in 2001 also included yellow-billed loon
observations in Elson Lagoon (Fischer 2001, p. 4; Fischer and Larned
2004, p. 146). During fixed-wing aerial surveys for common eiders in
late June of 1999 through 2007, between 23 and 99 yellow-billed loons
were observed in nearshore waters and along barrier islands of the
Beaufort and Chukchi Seas (Dau and Larned 2007, p. 18). Yellow-billed
loons used lagoons and nearshore waters along the coast of St. Lawrence
Island in summer in the 1950s (Fay and Cade 1959, pp. 92, 100). In
Russia, Solovyova (coastal boat surveys; 2007, p. 6) reported densities
of 0.24 birds/km\2\ using coastal waters near the Kyttyk Peninsula and
Ayon Island at the northern end of Chaun Bay in western Chukotka, and
0.04 birds/km\2\ at the southern end of Chaun Bay near the Chaun River
Delta in 2006. Vronskiy (1987, p. 30) observed individual yellow-billed
loons and pairs in bays 100-150 m (328-492 ft) offshore of northwestern
Taymyr during summer. Yellow-billed loons occurred in summer along the
coast of Wrangel Island, although there were no indications of nesting
on the island (Stishov et al. 1991, p. 20). In boat-based surveys in
the Kara and Barents Seas, arctic (Gavia arctica) and red-throated (G.
stellata) loons were abundant in the nearshore marine waters of the
western Kara Sea and in the Ob' and Yenisey estuaries, especially in
Baidaratskaya Bay, and occurred in smaller numbers in the Pechora Bay
in the Barents Sea in August and September 1995, but no yellow-billed
loons were observed (Decker et al. 1998, pp. 9, 11). In subsequent boat
surveys between 1998 and 2003, only one yellow-billed loon was observed
in mid-August 1998 in coastal waters northeast of Dolgy Island (west of
Vaigach Island) in the Pechora Sea (M. Gavrilo, in litt. 2008).
Wintering Habitat and Distribution
Wintering habitats include sheltered marine waters less than 30 m
(98.4 ft) deep, such as fiords and areas between islands on the inner
coast in Norway (Strann and [Oslash]stnes 2007, p. 2). Schmutz (2008,
p. 1) found that throughout migrating and wintering seasons, yellow-
billed loons marked with satellite transmitters occurred from 1 to 20
miles offshore. The wintering range includes coastal waters of southern
Alaska and British Columbia from the Aleutian Islands to Puget Sound;
the
[[Page 12936]]
Pacific coast of Asia from the Sea of Okhotsk south to the Yellow Sea;
the Barents Sea and the coast of the Kola Peninsula; coastal waters of
Norway; and possibly Great Britain (Earnst 2004, pp. 13-14; North 1993,
pp. 42-43; Ryabitsev 2001, p. 22; Schmutz in litt. 2008, p. 1; Strann
and [Oslash]stnes 2007, p. 2; Burn and Mather 1974, p. 278; Gibson and
Byrd 2007, p. 68). A small proportion of yellow-billed loons may winter
in interior lakes or reservoirs in North America (North 1994, p. 3).
Winter population distribution and numbers of yellow-billed loons
are not well documented, but some information is available from marine
bird surveys. Earnst (2004, p. 14) summarized loon observations in
boat-based marine bird population surveys in Lower Cook Inlet, Prince
William Sound, and Kodiak Island. In these surveys, estimates of
yellow-billed loons were in tens to low hundreds, with wide confidence
limits. In many cases, loons were not identified to species. Strann and
[Oslash]stnes (2007, p. 3) counted 1,160-1,605 yellow-billed loons on
surveys conducted off the coast of Norway from 1986 to 1994, confirming
Norway as the most important known wintering area for the species in
Europe. No surveys have been conducted in Asian wintering areas. In
some regularly used wintering areas such as the Yellow Sea, the
Aleutian Islands, and Great Britain, the yellow-billed loon's small
population and scattered marine distribution may have contributed to
the impression that yellow-billed loons are vagrants or rare visitors
(Lepage 2008, p. 1; Gibson and Byrd 2007, p. 68; Dudley et al. 2006, p.
533; Scott and Shaw 2008, pp. 241-248).
Immature loons and possibly some non-breeding adults stay in
wintering areas throughout the year (North 1994, p. 4). Earnst (2004,
pp. 11-12) summarized yellow-billed loon observations in summer marine
boat-based surveys conducted in lower Cook Inlet and Prince William
Sound in southcentral Alaska, and in southeast Alaska. Estimates from
all these surveys totaled only 339 yellow-billed loons, but many loons
were not identified to species (Earnst 2004, p. 11). In boat-based
surveys of murrelets conducted in July of 2002-2004 from Icy Bay to
LeConte Bay in southeast Alaska, Kissling et al. (2007, Appendices 7,
8) counted 20 yellow-billed loons. Yellow-billed loons have been
observed throughout summer months in the Aleutians (Gibson and Byrd
2007, p. 68). According to the Red Data Book of Kamchatka (2006, p.
92), non-breeding birds occur off the coast of Kamchatka in summer.
Migration
Yellow-billed loon migration routes are thought to be primarily
marine. Schmutz (in litt. 2008, p. 1) found that yellow-billed loons
marked with satellite transmitters generally remained between 1 and 20
miles from land during migration and winter. Yellow-billed loons
migrate singly or in pairs, but gather in polynyas (areas of open water
at predictable, recurrent locations in sea-ice covered regions), ice
leads (more ephemeral breaks in sea ice, often along coastlines), and
early-melting areas off river deltas near breeding grounds in spring
along the Beaufort Sea coast of Alaska and Canada (Barry et al. 1981,
pp. 29-30; Barry and Barry 1982, p. 25; Woodby and Divoky 1982, p. 406;
Johnson and Herter, 1989, p. 9; Barr 1997, pp. 12-13; Alexander et al.
1997, pp. 15, 17; Mallory and Fontaine 2004, pp. 52-53).
These observations of yellow-billed loons in the Beaufort Sea
during migration establish that at least some yellow-billed loons
breeding in Canada's Arctic Islands and along the adjacent Canadian
coast use this migration route. North (1993, pp. 45-46) examined
evidence of alternative migration routes for yellow-billed loons
wintering in southeast Alaska and British Columbia, suggesting that
they could migrate overland to mainland breeding areas in Canada,
particularly around Great Slave Lake. Yellow-billed loons have been
observed on inland lakes in Canada and Alaska (North 1993, pp. 43, 46).
The existence of this route is still hypothetical, and the number of
yellow-billed loons in interior mainland Canada is highly uncertain
(discussed below under Population Size).
Yellow-billed loons breeding in Alaska have been studied to
determine migration routes. Nineteen yellow-billed loons captured on
the ACP between 2002 and 2008 were outfitted with satellite
transmitters (Schmutz in litt. 2008, p. 1). All of them migrated to
Asia, predominantly south along the Russian coastline from the Chukotka
Peninsula (either through the Bering Strait or across the mountains
from the north side of the Chukotka Peninsula to the Gulf of Anadyr),
and along the Kamchatka coast. They wintered in the Yellow Sea and Sea
of Japan off China, North Korea, Russia, and Japan (near Hokkaido). All
10 yellow-billed loons fitted with transmitters on the Seward
Peninsula, Alaska, in 2007 and 2008 also used the Bering Strait region
after leaving breeding grounds. Five of these migrated to Asian grounds
as described above for ACP breeding birds; the other 5 wintered
throughout the Aleutian Islands from Shemya Island in the west to the
Semidi Islands off the coast of the Alaska Peninsula (Schmutz in litt.
2008, p. 1). Most of these yellow-billed loons departed breeding areas
in late September, arrived in wintering locations in mid-November,
started spring migration in April, and arrived on breeding grounds in
the first half of June; these dates are consistent with breeding ground
arrival dates reported by North (1994, p. 5). Non-breeders or failed
nesters may start fall migration in July.
The migration routes of yellow-billed loons breeding in Russia have
not been studied. Because of the proximity of the Chukotka Peninsula to
the ACP in Alaska, and the fact that ACP breeding yellow-billed loons
use the Chukotka Peninsula during migration (Schmutz in litt. 2008, p.
1), it is likely that some or all yellow-billed loons from eastern
Russia migrate through the Bering Strait to Asian wintering areas.
Population Size
ACP, Alaska
Yellow-billed loon population indices on the ACP of Alaska were
determined by two independent fixed-wing aerial transect surveys
conducted each year by the Service's Migratory Bird Management program.
Surveys were flown in early June each year from 1992 through 2008 (NSE
survey, 1992-2008, an average of 1,304 km\2\ (503.5 mi\2\) transect
area that sampled a total area of 30,465 km\2\ (11,763 mi\2\), for 4.3
percent coverage) and late June each year from 1986 through 2006 (ACP
survey, 1986-2006, average of 1,256 km\2\ (485 mi\2\) transect area
which sampled a total area 61,645 km\2\ (23,801 mi\2\), for 2.0 percent
coverage of a larger area than that covered by the NSE survey). The
average population index from the NSE survey is 1,119 yellow-billed
loons (95 percent confidence interval (CI) = 1,012 to 1,226, Larned et
al. 2009, p. 24). (Note: In order to estimate the reliability of a
sample statistic, such as an average, it is common to set confidence
limits to it (Sokal and Rohlf 1995, p. 139). The limits will show the
maximum and minimum numbers the statistic (e.g., average) is likely to
be, along with a measure of that likelihood (e.g., 95 percent). So,
when an average number of birds, for example, is reported, followed by
a confidence interval, the confidence interval shows the statistical
range of values that provides cutoff points for the likely values for
the average.) The long-term mean from the ACP survey is 2,611 loons (95
percent CI = 2,218 to 3,005; Mallek et al. 2007, p. 10; USFWS
unpublished data). The
[[Page 12937]]
confidence intervals around these 16- and 21-year means incorporate the
variation due to within-year sampling error, the spatial variability
among transects and within strata, and variation among years related
either to detection rate (observer ability, habitat change, weather
conditions) or the availability of birds to be seen (arrival or
departure of population components, behavior associated with nesting
chronology). One study integrated results from both the early and late
surveys, incorporating covariates adjusting for detection rates (Earnst
et al. 2005). The 12-year mean (1992 through 2003) resulted in an
estimate of 2,221 individuals (95 percent CI = 1,209-3,233) in early
June and 3,369 individuals (95 percent CI = 1,910-4,828) in late June
(Earnst et al. 2005, p. 295). Another estimate of population size was
determined by lake-circling aerial searches of greater than 7-ha (17.3-
acre) lakes on 7 x 7-km (4.35 x 4.35-mi) plots as part of a 2003-2004
study of yellow-billed loon habitat preferences (Stehn et al. 2005, pp.
1-37). This survey was flown from June 15 through 22 each year. Based
on average density observed, the estimated total population index was
2,544 (95 percent CI = 1,780-3,308) yellow-billed loons (Stehn in litt.
2008, p. 1).
Western Alaska
Seward Peninsula and Cape Krusenstern fixed-wing aerial lake-
circling surveys, on 12 x 12-km (7.46 x 7.46-mi) sample plots, were
flown in June of 2005 and 2007, and resulted in an estimate of 431 (95
percent CI = 280-582) yellow-billed loons on these western Alaska
breeding grounds (Bollinger et al. 2008, p. 1). Additional aerial
transects sampling an area of 15,234 km\2\ (5,882 mi\2\) were flown on
Selawik National Wildlife Refuge and adjacent wetlands in June in the
years 1996 and 1997 (Platte 1999, p. 3), but only three yellow-billed
loons were sighted, resulting in an estimated mean population index of
44 birds (95 percent CI = 0-95) (USFWS unpublished data). Yellow-billed
loons were documented nesting on St. Lawrence Island in the 1950s (Fay
and Cade 1959, pp. 84, 100), but there is no more recent information.
Adding western Alaska population figures to those from the ACP results
in an estimated total of 3,000 to 4,000 yellow-billed loons on breeding
grounds in Alaska.
Canada
Although overall breeding population estimates for yellow-billed
loons in Canada do not exist (https://www.bsc-eoc.org/clls-bw1.html,
accessed May 19, 2008), and yellow-billed loons are not summarized in
the Waterfowl Population Status annual reports compiled by the U.S. and
Canadian governments for North American Waterfowl (USFWS 2007, pp. 1-
62), several recent fixed-wing aerial waterfowl surveys included loon
observations in parts of Nunavut and Northwest Territories. Loons were
not the focus of the surveys, so it is possible that observer effort or
identification ability varied, and no visibility correction factors or
seasonal timing factors were applied. Helicopter surveys yielded
estimates ranging from 659 (SE 359) to 1,784 (SE 502) on northwest
Victoria Island, and from 98 (SE 70) to 258 (SE 146) birds in the
southwest part of the island (Raven and Dickson 2006). A fixed-winged
survey included Kent Peninsula and southeastern Victoria Island in
2005, and Queen Maud Gulf, King William Island, Rasmussen Lowlands, and
near Kugluktuk in 2006; all areas from both years were repeated in 2007
but with fewer transects sampled per unit area. The combined estimate
for both areas from 2005-2006 fixed-winged surveys and the 2007
estimate were similar, at 2,500-3,000 birds (Conant et al. 2006, p. 7;
Conant et al. 2007, p. 12; Groves in litt. 2008). Hines (in litt. 2008)
estimated there were 500-1,000 yellow-billed loons on Banks Island,
based on helicopter aerial surveys conducted in 1992 and 1993. The
range of these point estimates suggests that between 3,750-6,000 birds
occur on breeding grounds in the surveyed areas.
The rest of the yellow-billed loon's range on the Canadian mainland
has not been surveyed. Based on the vast number of large, fish-bearing
lakes north of treeline (an area of 500,000-750,000 km\2\) (193,051-
289,577 mi\2\) minus the surveyed areas on the mainland (46,000 km\2\),
(17,761 mi\2\) and using opportunistic observations of yellow-billed
loons by Northwest Territory and Nunavut checklist survey cooperators
over the last decade, Poter (in litt. 2008, p. 2, adjusted from Hines
in litt. 2008, p. 1) calculated that a density of 0.01-0.02 birds/km\2\
would yield an estimate of 4,500-14,000 birds in mainland breeding
areas in Canada, not including surveyed areas in the arctic described
in the previous paragraph. This estimate is based on a very large land
area bounded at the southern end by an area of documented yellow-billed
loon breeding between Great Slave Lake and Baker Lake, particularly in
or near the Thelon Game Sanctuary (North 1993, p. 42). Between this
area and the arctic coast is a large area where breeding has not been
documented (North 1993, Figure 2). Fair (2002, p. 30) estimated the
yellow-billed loon population on interior Canadian breeding grounds to
be 4,800, using a density of 0.02 loons in a 100,000 km\2\ area around
the Sanctuary, and a lower density of 0.007 for the wider area of
400,000 km\2\. Fair's estimate of 4,800 is close to the lower end of
Poter's (2008, p. 1) estimate of 4,500. We believe Fair's analysis more
accurately reflects likely yellow-billed loon distribution in Canada,
because it reflects a lower average density for the large area where
breeding has not been documented. Combining the 4,500 to 14,000
breeding birds estimated for interior Canada, and 3,750 to 6,000
breeding birds estimated for the arctic (and rounding to thousands), we
conclude that the Canadian breeding population size is 8,000 to 20,000,
but that it is most likely at the lower end of this range.
Russia
Information on the breeding-ground population size of yellow-billed
loons for Russia is limited. Hodges and Eldridge (2001, Appendix 2)
estimated 674 yellow-billed loons (coefficient of variation (C.V., a
measure of dispersion in a probability distribution) 0.55) in a
157,611-km\2\ (60,854-mi\2\) fixed-wing aerial survey area of the
eastern Siberia arctic coast from Kolyuchin Bay to the Lena River
Delta. We know of no other loon surveys within the breeding range of
the yellow-billed loon in Russia. Red Data Books for the Russian
Federation (2001, pp. 366-367), Yakutia (1987, p. 33), and the Northern
Far East of Russia (1998, pp. 97-98) do not offer population estimates.
Kondratiev (1989, p. 37) estimated that 2,000 birds nested in Chukotka,
but did not give a basis or sources for his estimate. Fair (2002, p.
31) projected, based on this estimate of 2,000 birds in Chukotka
(Kondratiev 1989, p. 37), that another 2,000 nested on the Taymyr
Peninsula, and that perhaps another 1,000 were scattered across the
arctic coast, giving 5,000 birds on Russian breeding areas.
Syroechkovsky (in litt. 2008) suggested (based on field observations
but not scientific surveys) that the number of birds on breeding
grounds (including non-breeding birds) is around 3,000 for Chukotka,
500 for Yakutia, and about 1,200 for Taymyr, for a total of around
4,700 birds. However, Solovyova (in. litt. 2008, p. 1; calculated from
Solovyova 2007, p. 6) recently estimated the post-breeding population
of the Kyttyk Peninsula on Chaun Bay in western Chukotka at 1,000, and
the post-breeding population of nearby Ayon Island at 900 birds. Given
[[Page 12938]]
Solovyova's (in. litt. 2008, p. 1) estimates for her study area in
Chukotka, she estimated that the total breeding ground population in
Chukotka might be as high as 5,000 birds. If the Chukotka population is
5,000, the total for Russia could be as high as 8,000 based on habitat
availability. Thus, our best information suggests the Russian breeding
population is between 5,000 and 8,000 birds.
In summary, the global breeding ground population size for yellow-
billed loons is unknown, but probably at the lower end of the range of
16,000 to 32,000. The Alaska population estimate of 3,000 to 4,000 is
derived from surveys. Less certain estimates based on the amount of
available habitat (plus limited survey data) are the lower end of the
range of 8,000 to 20,000 birds in Canada, and 5,000 to 8,000 in Russia.
Population Trend
Alaska
The only population trends available for yellow-billed loons
breeding in Alaska are on the ACP, where the ACP and NSE waterfowl
surveys are conducted. We note that because we count only the breeding
component of the population, the total population could decline without
being detected for a number of years. This could occur because
increased mortality of breeding birds could be masked by movements of
birds without territories (either sub-adult birds or adults which have
not found territories) into vacated territories. With this caution, we
believe the time series of at least 17 years for the surveys described
below gives us a reasonably reliable data set for observing population
trends, and these data represent the best information available at this
time.
A population growth rate, or lambda, less than 1.00 would indicate
population decline (negative ``growth''), while a lambda greater than
1.00 would indicate population growth. For the ACP survey 1986-2006,
the average growth rate was 0.9886 (95 percent CI = 0.9625-1.0154)
(Mallek et al. 2007, p. 21), and for the NSE survey 1992-2008 (a
smaller area than that covered by the ACP survey, and surveyed earlier
in June), the average growth rate was 1.016 (95 percent CI = 0.995-
1.036) (calculated from Larned et al. 2009, Figure 1). Thus, these
surveys provide slightly conflicting perspectives, with one suggesting
a stable or slightly declining population (with a point estimate of a
decline of 1.1 percent/yr.) and the other suggesting a stable or slight
increasing population (with a point estimate of an increase of 1.6
percent/yr.) on the ACP.
Earnst et al. (2005, pp. 289-304) sought to improve the estimates
above by using a statistical model that takes into account possible
confounding factors of survey type, spring timing, and observer
experience. They used this model to analyze ACP and NSE survey data
through 2003. Controlling for these confounding factors, they (p. 298)
estimated average population growth rate to be 0.991 (95 percent CI =
0.964-1.018), also indicating a stable or slightly declining
population.
We also examined a subset of the NSE data through 2008 that
included only the observations of the most consistent and experienced
pilot-observer, who has flown all 16 early-June NSE surveys during
1992-2008. Each survey includes observations of two observers: the
pilot-observer in the left-side seat of the aircraft, and a second
observer in the right-side seat. There have been numerous ``right-side
observers'' over the course of the NSE survey. Each of these observers
has a different ability to see and identify birds, and this ability
often increases over successive surveys as the observer gains
experience. Our analysis of the left-side pilot-observer eliminated the
necessity to estimate the variable magnitudes of influence of right-
side observer experience. In addition, the increased interest in
yellow-billed loons in 2002 may have influenced new right-side
observers to search more intensively for yellow-billed loons than
earlier observers, who focused on waterfowl. Our analysis of the pilot-
observer data from the NSE survey also eliminated the need to reconcile
the later timing and different survey extent of the ACP survey. The
average growth rate using this subset of data was slightly lower and
more precisely estimated at 0.986 (95 percent CI = 0.967-1.006) (USFWS
unpublished data) than the estimate of 0.991 from Earnst et al.'s
(2005, p. 298) model, and the results also indicate a relatively stable
or slightly declining population.
In summary, the information available from the ACP does not allow
us to precisely determine current population trends. Two surveys and
multiple analytical approaches used to control for confounding factors
provide estimates indicating trends ranging from slightly increasing to
slightly decreasing, and all estimates have 95 percent CIs that include
a lambda of 1.0, indicating that possible trends cannot be
distinguished from population stability with reasonable certainty.
Although the population trend on the ACP is uncertain, we conclude that
the number of breeding yellow-billed loons on the ACP breeding grounds
is either stable or declining slightly, with point estimates from
models controlling for confounding factors estimating decline on the
order of ~1 percent per year. We will continue to look for ways to
improve our ability to detect trends. Surveys in western Alaska have
not been conducted for a long enough period (2005 and 2007) to detect
trends.
Russia
In Russia, recent data are fragmentary, making it difficult to
determine trends. In the west, the Red Data Book of the Russian
Federation (2001, p. 366) stated that the species no longer nests in
European Russia where it was formerly found, such as the Kola
Peninsula, the archipelago of Novaya Zemlya, and Vaigach and Ainovy
Islands in the Kara Sea, although it is unclear how abundant or
widespread the species was in these areas historically. (However,
Kalyakin (2001, p. 10) reports finding it nesting on Novaya Zemlya,
although it is ``extremely rare.'') Similarly, according to the Red
Data Book of the Yamal-Nenets Autonomous District (1997) near the
western end of the Russian breeding range, in the previous 20 years
only a few non-breeding yellow-billed loons were recorded in the
District. Strann (in litt. 2008) speculated that since the early 1990s
there may have been a decline in the number of yellow-billed loons in
the main Norway wintering area, which would be consistent with a
western Russian breeding ground range contraction if birds nesting in
western Russia migrate to Norway for winter (which seems logical). We
were unable to find either the source of the Red Data Book statements
or supporting evidence for this potential range contraction. In eastern
Russia, yellow-billed loons apparently no longer nest along the
northern coast of the Sea of Okhotsk where they occurred 30-50 years
ago, nor on the Anadyr River delta (Red Data Book of the Russian
Federation 2001, p. 366; Red Data Book of the Northern Far East of
Russia 1998, p. 97). However, Solovyova (in litt. 2008) reported that
the number of breeding yellow-billed loons may be increasing in some
locations in eastern Siberia, specifically near Chaun Bay in western
Chukotka, and at Belyaka Spit near Kolyuchin Bay in northeastern
Chukotka.
In summary, we found unsubstantiated reports that the species may
no longer be found in parts of its historical range in Russia, but
there is somewhat contradictory information for some areas and a lack
of survey data for all areas. Yellow-billed loons may also be
increasing in some areas in Russia.
[[Page 12939]]
We conclude that we do not have reliable trend information for the
Russian breeding grounds.
Canada
As described above for Population Size, survey data for Canadian
breeding grounds cover a small portion of the range, and have not been
conducted for enough years to analyze trends. We conclude that we do
not have reliable trend information for Canadian breeding grounds.
To summarize rangewide population trend information, we have
reliable data indicating that the ACP breeding population is stable or
slightly declining. We do not have reliable evidence from other
breeding areas that breeding populations are increasing or decreasing.
There have been no surveys of yellow-billed loons on wintering areas,
so we have no trend information from those areas.
Population Resiliency
Certain intrinsic aspects of yellow-billed loon ecology and
demography, including low and variable productivity, adult survival,
and low population numbers, are relevant to the species' status. Stable
populations of K-selected species, such as the yellow-billed loon, are
characterized by low annual productivity rates balanced with high
annual survival rates, meaning that individuals must live many years to
replace themselves with offspring that survive to recruit into the
breeding population. Low productivity means that depleted K-selected
species have lower recovery potential and slower recovery rates
following population declines than r-selected species, which are
characterized by high annual productivity. Factors that reduce
productivity, including loss of productive breeding habitats, reduction
in prey populations, and increases in nest predators, may further
constrain K-selected species' recovery potential. Further, most arctic
species are characterized by variable annual productivity, given the
vagaries and severity of arctic weather, fluctuations in predator-prey
relationships, and other aspects of arctic ecology. The population
impact of threats that reduce productivity could be magnified if
coincident with an infrequent year of otherwise high productivity.
Although factors that compromise productivity can cause populations
to decline, adult survival is likely the more important determinant of
K-selected species' population size and persistence (Smith and Smith
2001, p. 235). If enough adults are removed from the population prior
to replacing themselves (i.e., adult survival is decreased), the
population will decline. Perhaps most pertinent to a discussion of
extinction, rare species--those with low numbers--are intrinsically
closer to a threshold below which recovery is not possible (i.e.,
minimum viable population) (Hunter 1996, p. 137).
These intrinsic aspects of yellow-billed loon ecology and
demography signal the continuing need to monitor yellow-billed loon
populations, despite the fact that the species continues to be widely
distributed across both its arctic breeding range, which is nearly
holarctic, and in its wintering range.
Factors Affecting the Yellow-Billed Loon
Section 4(a)(1) of the Act (16 U.S.C. 1533(a)(1)) and regulations
promulgated to implement the listing provisions of the Act (50 CFR part
424) set forth the procedures for adding species to the Federal Lists
of Endangered and Threatened Wildlife and Plants. A species may be
determined to be an endangered or threatened species due to one or more
of the five factors described in section 4(a)(1) of the Act. Below, we
provide a summary of our analysis of threats to the yellow-billed loon.
Factor A: Present or Threatened Destruction, Modification, or
Curtailment of the Habitat or Range
We considered whether yellow-billed loon habitats are threatened by
oil and gas development (including disturbance, changes in freshwater
chemistry and pollutant loads, and changes in freshwater hydrology), by
degradation of the marine environment from pollution or overfishing, or
by climate change. Potential threats from oil and gas development are
addressed by the petitioners under Factor E, but are discussed here
under Factor A because they are potential mechanisms for rendering
breeding habitats unsuitable. Potential direct impacts on loon
mortality associated with development, such as increased predation and
oil spills, are discussed under Factors C and E, respectively.
Terrestrial Oil and Gas Development
Terrestrial and marine oil and gas development occurs in the range
of the yellow-billed loon. Here we discuss terrestrial development in
Alaskan and Russian breeding grounds. We are not aware of any
terrestrial oil or gas development within the breeding range of the
yellow-billed loon in Canada; planned terrestrial development on the
Mackenzie River Delta is outside the breeding range, although activity
there could affect loons migrating through adjacent marine waters.
Marine activities related to oil and gas development are discussed
under Factor E.
Much of the yellow-billed loon's breeding habitat in Alaska is
within areas available for oil and gas leasing and development.
Approximately three-quarters of the yellow-billed loons that nest in
Alaska, and over 90 percent of those that nest on Alaska's ACP, occur
within the 9.5-million-ha (23.5-million-ac) NPR-A (Earnst et al. 2005,
p. 300), in areas that are leased or available for leasing for oil and
gas exploration and development. Approximately 29 percent of yellow-
billed loons breeding on the ACP nest in NPR-A tracts that have been
leased (Stehn and Platte, U.S. Fish and Wildlife Service, in litt.
2008, p. 1), and 25 exploration wells were drilled during the period
2000-2007 (https://www.blm.gov/ak/st/en/prog/energy/oil_gas/npra.html,
accessed 3 June 2008). The Northwest Planning Area (NW) NPR-A
Integrated Activity Plan/Environmental Impact Statement Record of
Decision (ROD) (USDOI-BLM 2004a, p. 5) has made 100 percent of the NW
NPR-A available for leasing. The Final NE NPR-A Supplemental Integrated
Activity Plan/Environmental Impact Statement ROD (USDOI-BLM 2008b, p.
1) allows leasing of 86 percent (1.6 million ha, or 3.94 million ac) of
the NE NPR-A immediately, and an additional 9 percent beginning in
2018. Virtually all yellow-billed loon breeding habitat in the NE NPR-A
is within areas currently available for leasing (USDOI-BLM 2008a,
Volume 6, Maps 2-4 and 3-10).
If offshore development occurs in the Chukchi Sea, it is
anticipated that a 500-km (300-mi) oil pipeline will be built across
the NPR-A from the coast between Icy Cape and Point Belcher to the
Trans-Alaska Pipeline (USMMS 2008, p. IV-10). The State of Alaska also
leases rights to oil and gas development on its land, including the
Colville River Delta (ADNR 2008, p. 1), where development has already
occurred within the range and habitats of the yellow-billed loon (ADNR
2008, p.1). Thus, as a result of past and possible future oil and gas
lease sales, and ongoing exploratory efforts, a significant portion of
the yellow-billed loon's breeding habitat in NPR-A is subject to
potential oil and gas development. Additionally, resource development
in adjacent offshore areas may result in the construction of pipelines
across breeding habitat in NPR-A.
Although lease sales and exploratory efforts set the stage for
possible future development in yellow-billed loon breeding habitat in
northern Alaska,
[[Page 12940]]
determining the likelihood and timing of eventual development is
difficult. In northeast NPR-A, several satellite production pads
associated with existing infrastructure and facilities outside NPR-A at
the Alpine field on the Colville River delta are in various stages of
planning, permitting, and construction. It is very likely that within
the next 10 to 20 years at least 5 to 7 satellite production pads
feeding the existing central processing facility will be in operation,
with some pads on State lands on the delta and some on adjacent Federal
lands in NPR-A. Elsewhere in NPR-A the likelihood and timing of
possible future development are more difficult to predict. BLM
estimates that exploratory activities take roughly 10 years before
construction begins (USDOI-BLM 2008c, p. 13), with roughly 70 years
from the initiation of exploration until final field abandonment.
Initial exploratory activities have commenced in some areas in NPR-A;
exploration has yet to begin on some existing leased tracts elsewhere;
and other lands have not yet been leased or offered for lease. Thus,
yellow-billed loon habitat in the Colville River delta and adjacent
NPR-A varies in its potential for future oil and gas development, and
the timing of development, where it occurs, will be staggered starting
with imminent development on and near the Colville River delta,
followed by exploration, construction, and production over a period of
several decades elsewhere, persisting for at least 70 years and
possibly longer in various areas.
Terrestrial oil development is ongoing, and likely to increase, at
the western edge of Russian yellow-billed loon breeding range. These
areas have never been systematically surveyed for loons, so the
historical occurrence and degree to which development areas overlaps
areas used by loons is unknown. On the Yamal Peninsula, the largest gas
field is the Bovanenkovskeo field, which is projected, beginning in
2011, to produce approximately 115 billion cubic meters (4 trillion
cubic ft) of gas, which will be transported by new railways and a
2,451-km (1,523-mi) long pipeline currently under construction (Barents
Observer 2008, p. 1). A liquefied-natural-gas plant is planned on the
Kara Sea coast of the peninsula. The Yuzhnoe-Khykchuyu oil field in the
Timan-Pechora province near the port of Varandey on the Pechora Sea is
among the largest in Russia, and is planned as an anchor field for
further development (ConocoPhillips 2008, p. 1). Major western Siberian
oil fields in the Pechora River basin of the Komi Republic have
operated for decades upstream of yellow-billed loon breeding range, and
a large mining industry operates out of Norilsk on the Taymyr
Peninsula. Gazprom, Russia's largest oil and gas company, is developing
new discoveries in Chukotka near Anadyr (Gazprom Neft 2004, p. 1). In
addition to these activities at the western edge of the Russian
breeding area, reserves exist but are not currently planned for
development in the Laptev formation on the arctic coast east of the
Lena River (USGS 2007, pp. 1-2).
We are not aware of any yellow-billed loon surveys in the Taymyr,
Timan-Pechora, and Yamal districts described above; so we do not know
whether or to what extent yellow-billed loon breeding habitat overlaps
with zones of industrial activity in this area. It is possible that the
reported potential contraction at the western edge of the yellow-billed
loon's range in Russia (Red Data Book of the Russian Federation 2001,
p. 366) could have resulted from the effects of resource extraction in
the region, but we have no evidence for or