Endangered and Threatened Wildlife and Plants; 12-Month Finding on a Petition To List the Bonneville Cutthroat Trout as Threatened or Endangered, 52235-52256 [E8-20674]
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Federal Register / Vol. 73, No. 175 / Tuesday, September 9, 2008 / Proposed Rules
Dated: August 26, 2008.
Michael K. Buckley,
Deputy Assistant Administrator for
Mitigation, Department of Homeland
Security, Federal Emergency Management
Agency.
[FR Doc. E8–20823 Filed 9–8–08; 8:45 am]
FOR FURTHER INFORMATION CONTACT:
Larry Crist, Field Supervisor, U.S. Fish
and Wildlife Service, Utah Ecological
Services Office (see ADDRESSES section).
If you use a telecommunications device
for the deaf (TDD), call the Federal
Information Relay Service (FIRS) at
800–877–8339.
SUPPLEMENTARY INFORMATION:
BILLING CODE 9110–12–P
DEPARTMENT OF THE INTERIOR
Fish and Wildlife Service
50 CFR Part 17
[FWS–R6–ES–2008–0023; 1111 FY07 MO–
B2]
Endangered and Threatened Wildlife
and Plants; 12-Month Finding on a
Petition To List the Bonneville
Cutthroat Trout as Threatened or
Endangered
Fish and Wildlife Service,
Interior.
ACTION: Notice of a 12-month petition
finding.
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AGENCY:
SUMMARY: We, the U.S. Fish and
Wildlife Service (Service), announce our
12-month finding on a petition to list
the Bonneville cutthroat trout
(Oncorhynchus clarkii utah) as a
threatened subspecies throughout its
range in the United States, pursuant to
the Endangered Species Act of 1973, as
amended (Act). After a thorough review
of all available scientific and
commercial information, we find that
listing the Bonneville cutthroat trout as
either threatened or endangered is not
warranted at this time. We ask the
public to continue to submit to us any
new information that becomes available
concerning the status of or threats to the
subspecies. This information will help
us to monitor and encourage the
conservation of the subspecies.
DATES: The finding in this document
was made on September 9, 2008.
ADDRESSES: This finding is available on
the Internet at https://
www.regulations.gov. Supporting
documentation we used in preparing
this finding is available for public
inspection, by appointment, during
normal business hours at the U.S. Fish
and Wildlife Service, Utah Ecological
Services Office, 2369 West Orton Circle,
Suite 50, West Valley City, Utah 84119;
telephone (801) 975–3330. Please
submit any new information, materials,
comments, or questions concerning this
finding to the above address or via
electronic mail (e-mail) at
paul_abate@fws.gov.
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Background
Section 4(b)(3)(B) of the Endangered
Species Act of 1973, as amended (Act)
(16 U.S.C. 1531 et seq.), requires that,
for any petition to revise the List of
Endangered and Threatened Species
that contains 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 the
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 List of Endangered and Threatened
Species. Section 4(b)(3)(C) of the Act
requires that a petition for which the
requested action is found to be
warranted but precluded be treated as
though resubmitted on the date of such
finding, that is, requiring a subsequent
finding to be made within 12 months.
Such 12-month findings must be
published in the Federal Register.
Previous Federal Actions
On February 26, 1998, we received a
petition, dated February 5, 1998, from
the Biodiversity Legal Foundation
requesting that the Service list the
Bonneville cutthroat trout
(Oncorhynchus clarkii utah) (BCT) as
threatened in U.S. river and lake
ecosystems where it continues to exist,
and to designate its occupied habitat as
critical habitat within a reasonable
period of time following the listing. On
December 8, 1998, we published a 90day petition finding for the BCT in the
Federal Register (63 FR 67640). We
found that the petition presented
substantial information indicating that
the subspecies may be warranted for
listing under the Act, and initiated a
review of the subspecies’ status within
its historic range.
In the 1998 90-day finding, we
solicited additional data, comments,
and suggestions from the public, other
governmental agencies, the scientific
community, industry, and other
interested parties concerning the status
of the BCT throughout its range. The
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comment period for submission of
additional information ended on
January 7, 1999, but was reopened (64
FR 2167) during January 13 through
February 12, 1999. We published a 12month finding in the Federal Register
on October 9, 2001 (66 FR 51362), and
documented that the BCT was not
warranted for listing under the Act
because it was neither endangered nor
likely to become endangered within the
foreseeable future throughout all or a
significant portion of its range.
On February 17, 2005, we were sued
by the Center for Biological Diversity,
and others, on the merits of the 12month finding. On March 7, 2007, the
District Court of Colorado dismissed the
lawsuit after determining that Plaintiffs
failed to demonstrate the not warranted
finding was arbitrary, capricious, or
contrary to law. The Plaintiffs appealed
to the 10th Circuit Court of Appeals on
May 4, 2007.
On March 16, 2007, in the interim
between the lawsuit dismissal and
appeal, the Solicitor of the Department
of the Interior issued a formal opinion
regarding the legal interpretation of the
term ‘‘significant portion of the range’’
of a species (DOI 2007). The opinion
provides guidance on analysis intended
to determine whether a species is in
danger of extinction throughout a
significant portion of its range when it
is not in danger of extinction throughout
its entire current range. Because this
opinion was pertinent to the BCT
decision, we withdrew the 2001 12month finding for BCT (USFWS 2007,
entire), and initiated a new status
review to include significant portion of
the range analysis. We published a
notice in the Federal Register (73 FR
7236) announcing the opening of a
comment period from February 7
through April 7, 2008. The notice
specified that the new status review
would include consideration and
analysis of all information previously
submitted, and any new information
provided regarding the status of the
BCT.
Species Biology
The BCT is native to the Bonneville
basin, and is 1 of 14 subspecies of
cutthroat trout recognized by Behnke
(1992, pp. 3–21, 132–138) that are
native to interior regions of western
North America. BCT generally have
large, evenly distributed spots, but a
high degree of intra-basin variation
exists. BCT tend to develop large,
pronounced spots that are evenly
distributed on the sides of the body
rather than concentrated posteriorly as
in the Yellowstone cutthroat trout
(Oncorhynchus clarkii bouveri)
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subspecies. Coloration in BCT is
generally dull compared to other
cutthroat subspecies; however,
coloration can vary depending on
environmental conditions and local
genetic composition (Behnke 1992, pp.
132–138).
Vertebrae typically number 62–63,
slightly higher than in other subspecies.
Scales in lateral series average 150–170.
BCT average between 16–21 gill rakers,
with a mean of 18–19, except the Snake
Valley type, which have 18–24 (mean,
20–22). Another important
characteristic of all cutthroat subspecies
is the presence of basibranchial teeth,
which are absent in rainbow trout
(Behnke 1992, p. 132). Numbers of
basibranchial teeth provide information
about subspecies derivation and
relatedness. The Snake Valley type have
profuse basibranchial teeth, averaging
20–28, while most other BCT average 5–
10 (Behnke 1992, p. 132).
Life strategies exhibited by BCT
include stream resident (occupy home
ranges entirely within relatively short
reaches of streams), fluvial (migrate as
adults from larger streams or rivers to
smaller streams to reproduce), adfluvial
(migrate, sometimes many kilometers, as
mature adults from lakes to inlet or
outlet streams to spawn), and lacustrine
(lake) forms. The life strategy that a
particular BCT population exhibits
likely depends on a combination of
environmental conditions and genetic
plasticity of inherited traits. Very little
information is available to suggest the
extent of plasticity and what
environmental characteristics may cue a
successful shift in life strategy. Most
information is based on the success or
failure of transplants of various life
forms among different aquatic
ecosystems. Furthermore, evidence
suggests that BCT populations within a
single stream can comprise multiple life
history strategies (resident, fluvial,
adfluvial), and that individuals may use
mainstem rivers to move between and
among drainages where they are not
fragmented by water diversions or
barriers (Kershner et al. 1997, entire).
May et al. (1978, p. 19) found that
male BCT sexually matured at age 2
while females matured at 3 years of age.
However, Bear Lake BCT were reported
to mature much later, with adults
normally beginning to mature at 5 years
of age but not spawning until age 10
(Neilson and Lentsch 1988, p. 131).
Both the age at maturity and the annual
timing of spawning vary geographically
with elevation, temperature, and life
history strategy (Behnke 1992, p. 136;
Kershner 1995, pp. 28–30). Lake
resident trout may begin spawning at 2
years and usually continue throughout
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their lives, while adfluvial individuals
may not spawn for several years
(Kershner 1995, pp. 28–30). Annual
spawning of BCT usually occurs during
the spring and early summer at higher
elevations at temperatures ranging from
4–10 °C (May et al. 1978, p. 19). May et
al. (1978, p. 19) reported BCT spawning
in Birch Creek, Utah, beginning in May
and continuing into June. BCT in Bear
Lake began spawning in late April and
completed spawning in June (Nielson
and Lentsch 1988, p. 131). The wild
broodstock at Manning Meadow
Reservoir (9,500 feet elevation) spawn
from late June to early July (Hepworth
and Ottenbacher 1997, p. 1). In Lake
Alice, Wyoming, fish were predicted to
spawn from late May until mid-June
(Binns 1981, p. 47).
Fecundity of cutthroat is typically
1,200–3,200 eggs per kilogram (kg) (2.2
pounds (lbs)) of body weight (Behnke
1992, p. 33). In Birch Creek, a 147
millimeters (mm) (5.8 inches (in)) BCT
female produced 99 eggs, a 158 mm (5.8
in) female produced 60 eggs and a 176
mm (6.9 in) female produced 176 eggs
(May et al. 1978, p. 19). Whereas in
Raymond Creek, Wyoming, 3 females
ranging from 124 to 246 mm (4.9 to 9.7
in) averaged 165 eggs (Binns 1981, p.
48). Evidence suggests fecundity of lakedwelling BCT is greater. Fecundity of
females in Lake Alice averaged 474
eggs/female (Binns 1981, p. 48), while
females in Manning Meadow, Utah,
averaged 994 eggs/female (D. Hepworth,
Utah Division of Wildlife Resources,
unpubl. data). Incubation times for wild
BCT have not been verified, but Platts
(1957, p. 10) suggested eggs hatch and
fry begin to emerge approximately 45
days after spawning, depending on
temperature.
Larvae typically emerge in mid-to-late
summer, depending on spawning times.
Once emerged, larvae or fry, as they are
commonly called, are poor swimmers
and typically migrate to stream margins.
Adfluvial BCT spend 1 or 2 years in
streams before migrating to the Lake
(Nielson and Lentsch 1988, p. 131).
Growth of resident BCT is highly
dependent on stream productivity. In
general, growth of trout tends to be
slower in high-elevation headwater
drainages than in lacustrine
environments, but this likely depends
on temperatures and food base. In Birch
Creek, Utah, age 1 fish averaged 84 mm
(3.3 in), age 2 fish averaged 119 mm (4.7
in), age 3 fish averaged 158 mm (6.2 in),
and age 4 fish averaged 197 mm (7.8 in)
in length (May et al. 1978, p. 17).
Growth in two Wyoming streams was
faster, and age 4 fish averaged 282 to
320 mm (11.1 to 12.6 in) in length
(Binns 1981, p. 44). In contrast, BCT in
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Bear Lake grow to an average size of 560
mm (22.0 in) and 2 kg (4.4 lbs) (Nielson
and Lentsch 1988, p. 131). Historic
accounts of BCT in Utah Lake suggest
fish may have reached a meter in length
(Notes from Yarrow and Henshaw in
1872 as described by Tanner 1936).
Platts (1957, p. 10) reported that some
BCT taken from Utah Lake a century ago
attained weights of over 11.3 kg (25 lbs).
Little is known about feeding habits of
BCT. In general, BCT trout are
insectivorous, especially in stream
habitats. Both terrestrial and aquatic
insects appear to be important to their
diet (May et al. 1978, pp. 7–10; Binns
1981, p. 48). In Birch Creek, May et al.
(1978, pp. 9–10) reported BCT diets
were diverse in summer, while in the
fall in Trout Creek, Utah, their diet
consisted primarily of terrestrial insects.
Dipterans and debris were the dominant
food items for immature trout, while
terrestrial insects were the dominant
prey for mature individuals. BCT may
display more plasticity in feeding habits
depending on the system or specific
population characteristics. Little
information has been collected on BCT
to understand the extent of feeding
shifts of BCT. Platts (1957, p. 4)
suggested that cutthroat do not need to
feed on fish to attain large sizes but will
do so where insects are not abundant.
Interactions With Nonnative Fish
BCT may or may not persist when
nonnative trout are stocked into BCT
waters. The actual mechanism that
dictates the survivorship of BCT in the
presence of nonnatives is unknown, but
the recent discovery that numerous BCT
populations have persisted for decades
in the presence of rainbow trout
(Oncorhynchus mykiss), Yellowstone
cutthroat trout, and other nonnatives
suggests BCT is not always displaced by
nonnatives as previously thought.
However, BCT can hybridize with
rainbow trout and Yellowstone
cutthroats in some situations and be
displaced by the superior competitor,
brook trout (Salvelinus fontinalis). The
degree of hybridization appears to vary
with the persistence of the stocked fish
and also with habitat conditions as does
the level of competition with brook
trout.
Benhke (1992, p. 107) reported that
BCT native to the Bear River drainage
adapted to the harsh and fluctuating
environments of desert basin streams,
remaining the dominant trout today in
many streams where nonnative trout
were introduced. This seems to be a
fairly unique trait of BCT compared to
other cutthroat subspecies. There is still
no specific rationale as to why BCT
would persist better than other desert
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cutthroat subspecies, yet something in
its unique genetic composition seems to
allow BCT to persist where other
cutthroat subspecies have been found to
be displaced.
For example, Bear Lake BCT, probably
due to the unique environmental
conditions in which they developed,
have resisted hybridization with and
replacement by nonnative trout.
Yellowstone cutthroat trout,
Yellowstone cutthroat rainbow trout
hybrids, and rainbow trout were
consistently stocked into Bear Lake for
decades. Benhke (1992, p.137)
examined specimens from Bear Lake
and compared these to museum
specimens from the lake and with
cutthroat trout from the Bear River
drainage and found no evidence of
hybridization among their taxonomic
characters. Nielson and Lentsch (1988,
p.130) similarly reported that, after
examining the DNA of 52 Bear Lake
specimens, no rainbow trout alleles
were observed in any fish.
Since the early 1990’s, many
additional remnant BCT populations
have been found in streams that had
been stocked with rainbow trout or
Yellowstone cutthroat trout (Utah
Division of Wildlife Resources,
unpublished data). These BCT
populations were assumed to be lost
through hybridization until recent
surveys found BCT present. Results of
these surveys suggest BCT have retained
much of their natural genetic integrity
despite intensive nonnative stocking
efforts.
Introduced brook trout have been
stocked, legally and illegally, into some
BCT waters. BCT do not hybridize with
brook trout, but brook trout are thought
to acquire resources better and
reproduce and recruit more efficiently
than BCT. The specific mechanism of
how brook trout displace BCT is
unknown, but greater fecundity, earlier
maturity, and tolerance of higher
densities gives brook trout an advantage
over the native BCT (Griffith 1988, p.
105; Fausch 1989, pp. 307–312). The
extent of threat to BCT from brook trout
varies depending on environmental
conditions of the stream. Although not
considered the greatest threat to the
persistence of BCT, competition from
introduced brook trout can and has
displaced native BCT populations.
Habitat Requirements
Trout, regardless of their evolutionary
history, require 4 types of habitat during
various stages of their life history:
spawning habitat, nursery or rearing
habitat, adult habitat, and overwintering
habitat. Spawning gravels are required
for spawning success and can be a
limiting factor in high-gradient streams
where the current carries off suitable
spawning gravel (Behnke 1992, p. 25).
Conversely, an even greater concern
may be accumulation of fine sediments
into interstitial spaces of spawning
gravels, which prevents egg incubation
and reduces larval survival. Such fines
can become dominant in the sediments
when poor land-use practices alter flow
regimes, remove riparian vegetation,
and/or degrade overall watershed
conditions. These human-induced
activities can aggravate already fragile
soils and geology in vulnerable desert
climates.
Little information is available on
specific habitat requirements for BCT;
however, there is a wealth of
information on salmonid habitat
conditions in general which appear to
generally represent those of BCT
(Pennak and Van Gerpen 1947, entire;
Binns and Eiserman 1979, entire;
Scarnecchia and Bergersen 1987, entire).
For example, well-oxygenated water,
cooler temperatures in general and a
complexity of instream habitat
structure, such as large woody debris
and overhanging banks, are considered
good trout habitat conditions. For
various species, subspecies, and local
forms, adaptations and tolerance of
these conditions varies. BCT have also
been found to survive and be fairly
robust in what is considered marginal
salmonid habitat conditions (e.g., turbid
water, fine sediments, warmer
temperatures, poor structural habitat).
This may be because BCT have evolved
in a desert environment where climate
can cause fluctuations in water and
sediment regimes and environmental
condition (Behnke 1992, p. 107).
It was previously thought that with
the exception of three lacustrine
systems, Bear Lake (Utah and Idaho),
Utah Lake, and Alice Lake (Wyoming),
BCT were historically found in cool
headwater streams throughout the
Bonneville basin. However, more recent
research and status and genetic surveys
reveal BCT populations are found at
high, moderate, and low elevations
(within the range of elevations in the
Bonneville Basin) in small headwater
streams, such as those of the north slope
of the western Uintas, to larger
mainstem rivers, such as the Thomas
Fork of the Bear River (UDWR,
unpublished data).
Historic Habitat
BCT likely historically occupied all
suitable habitats within the Pleistocene
Lake Bonneville basin, which included
portions of Idaho, Nevada, Utah, and
Wyoming. The desiccation of ancient
Lake Bonneville about 8,000 years ago
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likely fragmented the BCT into
remaining streams and lakes throughout
the basin, resulting in several slightly
differentiated groups of BCT, including:
(1) The Bear River basin; (2) the
Bonneville basin proper, including the
Wasatch Mountain and Sevier River
drainages; and (3) the Snake Valley, an
arm of ancient Lake Bonneville that was
isolated during an earlier desiccation
event (Behnke 1992, pp. 132–138).
There is general consensus among the
scientific community, including the
Service, that all these groups represent
the BCT subspecies (Shiozawa 2008, p.
1). For the purposes of this finding, all
three groups are considered BCT.
The BCT Conservation Team, which
includes biologists from Wyoming Game
and Fish Department (WGFD), Utah
Division of Wildlife Resources (UDWR),
Nevada Division of Wildlife (NDOW),
Idaho Department of Fish and Game
(IDFG), Bureau of Land Management
(BLM), U.S. Forest Service (USFS), the
National Park Service (NPS), and the
Service, completed a status report (May
and Albeke 2005) that describes the
rangewide status of BCT in the United
States. The rangewide status report
summarized the best available
information on BCT (May and Albeke
2005, pp. i, 16, 103–104). The status
report was peer reviewed by five
recognized experts in the fields of
fishery biology, conservation biology,
and genetics. The peer reviewers found
that the status report provided sound
scientific data to use in this 12-month
finding.
The 2001 finding on Bonneville
Cutthroat Trout included 28,863
hectares (71,322 acres) of lake habitat
(indicated as an adfluvial life history)
(USFWS 2001, pp. 34, 44, 50, 75). The
2005 BCT rangewide status report relied
on a protocol that was not designed to
address lake populations; however, 8
lakes connected to occupied stream
habitat were included as 412 stream
kilometers (km) (256 stream miles (mi))
(May and Albeke 2005, pp. 107, 110,
120). Thus, throughout the remainder of
the document, all occupied BCT habitat
is reported as stream habitat and
includes lake populations. These lake
populations are an important
component in conserving BCT, and
some lakes are specifically designated to
preserve genetically pure populations
(Donaldson 2008, pp. 8–9).
The BCT Conservation Team’s status
report included an analysis of probable
historic distribution (May and Albeke
2005, pp. 6, 16–19). Our understanding
of BCT historic distribution is based on
habitat thought to be occupied around
1800. The determination of occupation
in this era was based on historic
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climactic conditions, stream channel
gradient, barriers that would preclude
fish, and expertise of fishery biologists
familiar with each watershed. The
analysis resulted in 10,876 (km) (6,758
mi) of stream habitat potentially
occupied historically (May and Albeke
2005, pp. 6, 16–19). This analysis
included estimated stream miles for
historically occupied BCT lakes because
the analysis protocol was not designed
to address lake populations separately.
The historically occupied habitat
identified in each State included:
Utah—7,916 km (4,919 mi) (73 percent);
Idaho—1,854 km (1,152 mi) (17
percent); Wyoming—974 km (605 mi) (9
percent); and Nevada—132 km (82 mi)
(1 percent) (May and Albeke 2005, pp.
6, 16–19). The United States is divided
and sub-divided into successively
smaller hydrologic units that are
classified into four levels: regions, subregions, accounting units, and
cataloging units. Fourth-level
hydrologic unit codes (HUCs) in the
Lake Bonneville Basin, including Pine
Valley, Tule Valley, Pilot-Thousand
Springs, Northern Great Salt Lake
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Desert, Lower Beaver, and Sevier Lake,
were not included as historical habitats
because they were judged unsuitable
due to extreme conditions, because
information on them prior to 1800 is
unavailable, or because historical
records indicate that they were devoid
of fish.
Current Distribution
Current distribution of BCT is
approximately 3,830 km (2,380 mi)—35
percent of the probable historically
occupied stream miles (May and Albeke
2005, p. 19). Currently occupied habitat
identified in each State includes Utah—
2,438 km (1,515 mi) (64 percent);
Idaho—869 km (540 mi) (23 percent);
Wyoming—476 km (296 mi) (12
percent); and Nevada—47 km (29 mi) (1
percent) (May and Albeke 2005, p. 19).
The BCT is well distributed
throughout its range in four watershedbased GMUs (see Figure 1; Table 1
below). In earlier assessments, five
GMUs or GUs (geographic units) were
identified as including current
populations of BCT; however, we
combined the Bear Lake and Bear River
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GMUs because they occur within one
watershed, and our analysis was
conducted by watershed (May and
Albeke 2005, pp. 4–5). This
reconfiguration of GMUs does not imply
a reduction in the geographic area
where BCT occur (May and Albeke
2005, pp. 2–5).
Within each GMU, streams were
identified to the 4th-level hydrologic
unit and assigned to a HUC. BCT
occupy habitat in 22 of the 23 HUCs
determined to likely have supported
historical habitat. BCT also occupy
habitat in three HUCs that are either
partially or totally outside of the
subspecies historic range (May and
Albeke 2005, pp. 19–20); most of these
populations were reintroduced into
suitable habitat with no record of
nonnative fish (Behnke 1992, pp. 134–
135). The Bear River GMU has the
greatest extent of currently occupied
BCT habitat (2,010 km/1,249 mi),
followed by the Northern Bonneville
(1,532 km/952 mi), Southern Bonneville
(187 km/116 mi), and the West Desert
(101 km/63 mi).
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TABLE 1—FROM MAY AND ALBEKE 2005, (P. 19), TABLE 21 (P. 34)
Km (mi) currently
occupied by BCT
GMU name
Number of BCT
conservation
populations
Km (mi) occupied
by BCT
conservation
populations
Bear River ..................................................................................................................
Northern Bonneville ...................................................................................................
Southern Bonneville ...................................................................................................
West Desert ...............................................................................................................
2,010 (1,249)
1,532 (952)
187 (116)
101 (63)
33
65
21
34
1,753 (1,089)
1,318 (819)
145 (90)
101 (63)
Totals ..................................................................................................................
3,830 (2,380)
153
3,316 (2,061)
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Hybridization
Hybridization is a concern for many
cutthroat trout populations. An
introgressed population results when a
nonnative species or subspecies is
introduced into or invades native
cutthroat trout habitat, the two species
then interbreed (i.e., hybridize), and the
resulting hybrids survive and
reproduce. If the hybrids backcross with
one or both of the parental species,
genetic introgression occurs. Continual
introgression can eventually lead to the
loss of genetic identity of one or both
parent species, thus resulting in a
‘‘hybrid swarm’’ consisting entirely of
individual fish that often contain
variable proportions of genetic material
from both of the parental species.
Our criteria for considering the
potential impact of introgressed
populations of BCT are consistent with
a position paper, titled ‘‘Genetic
Considerations Associated with
Cutthroat Trout Management,’’
developed by the fish and wildlife
agencies of the intermountain western
States (UDWR 2000a, pp. 1–9).
Signatories to the position paper
include the IDFG, Montana Fish
Wildlife and Parks, NDOW, New
Mexico Game and Fish Department,
UDWR, and WGFD. The document
identified, for all subspecies of inland
cutthroat trout, three tiers of natural
populations for prioritizing
conservation and management options
under State fish and wildlife
management authorities: (1) Core
conservation populations composed of
greater than 99 percent cutthroat trout
genes; (2) conservation populations that
generally ‘‘have less than 10 percent
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introgression, but in which
introgression may extend to a greater
amount depending upon circumstances
and the values and attributes to be
preserved’’; and (3) cutthroat trout sport
fish populations that, ‘‘at a minimum,
meet a species’’ phenotypic expression
defined by morphological and meristic
characteristics (counts of body parts) of
cutthroat trout.’’
The premise of the position paper on
genetic considerations was that
populations must conform, at a
minimum, to the morphological and
meristic characteristics of a particular
cutthroat trout subspecies in order to be
included in a State’s conservation and
management plan for that subspecies.
Conservation populations of a cutthroat
trout subspecies include fish believed to
have uncommon or important genetic,
behavioral, or ecological characteristics
relative to other populations of the
subspecies. Sport fish populations,
conversely, while conforming
morphologically (and meristically) to
the scientific taxonomic description of
the subspecies, do not meet the
additional genetic criteria of
conservation or core, and are managed
for their value as sport fish rather than
for conservation of the subspecies.
Following the State management
agencies’ position paper (UDWR 2000a,
pp. 1–9), a ‘‘core population’’ is
genetically unaltered (pure), and a
‘‘conservation population’’ is pure (a
core population) or slightly introgressed
(typically less than 10 percent) due to
past hybridization, yet has attributes
worthy of conservation. Therefore,
conservation populations include both
core populations (genetically pure) and
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populations that are less than 10 percent
introgressed with rainbow trout or other
subspecies of cutthroat trout (May and
Albeke 2005, p. 71). The BCT rangewide
status report (May and Albeke 2005, p.
31) identified 153 stream populations
(3,316 km/2,061 mi) as conservation
populations (see Table 1, above, and
Figure 2). Of the 153 conservation
populations, 73 (732 km/455 mi) are
considered core populations containing
genetically pure BCT.
We consider all core and conservation
populations, as defined under the
States’ standards and as described by
May and Albeke (2005, p. 31), for
purposes of conducting this status
review. Because the categories are
nested (conservation populations
include core populations), we refer to
them collectively as ‘‘BCT conservation
populations’’ in the remainder of this
finding. Some of the data presented in
May and Albeke (2005) pertains to all
BCT populations (including sport fish)
or habitat. Those areas of this document
that do not specify ‘‘conservation
populations,’’ therefore, are referring to
all BCT populations. We conducted our
analysis on conservation populations
because we found that BCT with less
than 10 percent introgression still
express important behavioral, life
history, or ecological adaptations of
indigenous populations within the
range of the subspecies, and remain
valuable to the overall conservation and
survival of the subspecies (Campton and
Kaeding 2005, pp. 1323–1325). (See also
Factor E, Hybridization with Nonnative
Fishes.)
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Conservation Populations
Designated BCT conservation
populations exist throughout the
subspecies’ historic range (May and
Albeke 2005, p. 31)—in all four States
and in the four designated GMUs. BCT
currently occupy some habitat in 22 of
the 23 HUCs historically occupied, and
BCT that meet the conservation
population definition (less than 10
percent introgressed) exist in 19 of those
HUCs. BCT conservation populations
were also identified in two HUCs
(Spring-Steptoe and Hot Creek-Railroad
Valley) outside historic range, and three
additional conservation populations
were identified outside historical range
within the Upper Virgin HUC. The
majority of conservation populations
(65) occur in the Northern Bonneville
GMU occupying 1,318 km (819 mi). The
remainder of BCT conservation
populations are relatively equally
distributed among the West Desert (34),
Bear River (33), and Southern
Bonneville (21) GMUs. These
populations occupy 101 km (63 mi),
1,753 km (1089 mi), and 145 km (90 mi)
respectively (May and Albeke 2005, p.
34).
The majority of BCT conservation
populations (101; 66 percent) occur as
isolated, non-networked populations
(May and Albeke 2005, p. 34); 25
populations (16 percent) are weakly
connected; 15 populations (10 percent)
are moderately connected; and 12
populations (8 percent) have migratory
forms and open migration corridors that
make them strongly connected. The
strongly connected populations occur in
Utah, Idaho, and Wyoming in the Bear
River Geographic Management Unit
(GMU) and Northern Bonneville GMU
(May and Albeke 2005, pp. 34, 107, 115,
117).
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BCT Population Trend
BCT population trend and status can
be interpreted from results of previous
assessments conducted from the early
1970’s through the present time.
Hickman (1978, pp. 121–122) identified
approximately 15 populations he
considered ‘‘pure’’ occupying
approximately 34 km (21 mi) of stream
habitat. Duff (1988, pp. 121–127)
reported 41 ‘‘genetically pure’’ BCT
populations (39 stream populations) in
association with 304 km (189 mi) of
stream habitat. A draft Service status
review that was never finalized reported
48 genetically pure BCT populations
throughout the Bonneville Basin
(USFWS 1993, pp. 1–62). Duff (1996,
pp. 38–39) further refined his BCT
population distribution reporting 81
genetically ‘‘pure’’ populations
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occupying 377 km (234 mi) of stream
habitat. A Service status review found
that BCT occupied a total of 1,372 km
(852 mi) of stream habitat and 28,352 ha
(70,059 acres) of lake habitat totaling
291 populations (USFWS 2001, pp. iv–
v).
BCT assessments conducted between
1978 and 1996 generally counted
populations that were thought to be
genetically ‘‘pure.’’ The 2001 Service
assessment determined the genetic
status of each population but was more
inclusive and counted management,
conservation, and potential
conservation populations (USFWS 2001,
pp. viii–xi). The May and Albeke (2005)
assessment assessed the genetic status of
each BCT population and then
categorized genetic status based on the
criteria in the State’s genetic position
paper (UDWR 2000a, pp. 1–9).
Methods for tallying the number of
individual BCT populations tended to
vary by individual assessment, with
earlier assessments tending to split
tributary populations from mainstem
river reaches. In contrast, methods used
for the May and Albeke (2005, p. 64)
assessment tended to group populations
by higher order streams, thereby
reducing the total count of populations.
Thus, it is important to consider
changes in the amount of occupied
habitat when assessing population
trends from different assessments rather
than to simply rely on changes in
number of populations. The number of
known stream miles occupied by BCT
conservation populations increased over
time from 15 populations in 34 km (21
mi) of habitat in 1978 to 153
populations in 3,316 km (2,061 mi) in
2004. Some of the increase in BCT
conservation populations and their
habitat is the result of conservation
actions such as the discovery of more
populations in recent years; the
expansion or restoration of populations;
and the eligibility of populations for
conservation status (through genetic
testing) that were previously considered
hybridized. Increases in the amount of
BCT conservation population habitat is
also due to the use of a more accurate
GIS-based assessment method that
incorporated the National Hydrography
Dataset geodatabase (May and Albeke
2005, p. 2) and also the inclusion of
lakes as river miles as used in the most
recent assessment protocol (see above),
although the increase due to the
inclusion of lakes in the river mile
calculation only accounts for an
additional 412 km (256 mi) of stream
habitat.
The BCT Conservation Team’s most
recent analysis of the number of BCT
conservation populations and the extent
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of their habitat indicates that
conservation populations have
increased from 153 populations in 3,316
km (2,061 mi) in 2004 (May and Albeke
2005, p. 31), to 172 populations in 3,333
km (2,071 mi) in 2008 (Burnett 2008a,
entire). This most recent evaluation of
the BCT Conservation Team’s database
was cursory and was not performed for
other population parameters discussed
in May and Albeke (2005) (i.e.,
restoration activities, genetic status,
population health and densities, etc.);
however, it does indicate that the
number of BCT conservation
populations and their habitat continue
to increase.
Summary of Factors Affecting the
Species
Section 4 of the Act (16 U.S.C. 1533),
and implementing regulations at 50 CFR
424, set forth procedures for adding
species to the Federal Lists of
Endangered and Threatened Wildlife
and Plants. In making this finding, we
summarize information regarding the
threats to the BCT in relation to the five
factors provided in section 4(a)(1) of the
Act.
In making this finding, we considered
all scientific and commercial
information that we received or
acquired up to the publication of the
2001 12-month finding (66 FR 51362),
and after publication of the notice
initiating this finding (73 FR 7236;
February 7, 2008). We relied primarily
on published and peer-reviewed
documentation for our conclusions, and
most significantly, the rangewide status
report competed by the BCT
Conservation Team (May and Albeke
2005, entire).
Pursuant to section (4) of the Act, a
species may be determined to be an
endangered or threatened species on the
basis of any of the following five factors:
(A) Present or threatened destruction,
modification, or curtailment of habitat
or range; (B) overutilization for
commercial, recreational, scientific, or
educational purposes; (C) disease or
predation; (D) inadequacy of existing
regulatory mechanisms; or (E) other
natural or manmade factors affecting its
continued existence. We evaluated
whether threats to the BCT may affect
its survival. Our evaluation of threats,
based on the best scientific and
commercial information available, is
presented below.
Factor A. The Present or Threatened
Destruction, Modification, or
Curtailment of the Species’ Habitat or
Range
Land use activities associated with
each BCT conservation population were
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identified and documented in May and
Albeke (2005, p. 52, Table 30), but the
significance of the activities was not
determined in relation to individual
populations or to the conservation of the
subspecies. Non-angling recreation
(camping, hiking, ATV use, etc.) occurs
in 69 percent of the conservation
populations. Livestock grazing occurs in
58 percent of the conservation
populations, roads in 69 percent, timber
harvest in 20 percent, and dewatering in
30 percent. Hydroelectric plants, water
storage, or flood control occurs in 20
percent of the conservation populations.
A small percentage of populations have
mining or nonnative fish stocking. Many
populations have more than one land
use occurring in the area.
A comprehensive assessment of the
effects of land management practices on
BCT does not exist. However, an
evaluation of habitat quality was
conducted for currently occupied
habitat (May and Albeke 2005, p. 26).
The evaluation considered both natural
habitat features and human-caused
disturbances. A stream ranked as
‘‘excellent’’ if it had ample pool habitat,
low sediment levels, optimal
temperatures, and quality riparian
habitat. A ‘‘good’’ habitat quality rating
indicated the presence of some less than
ideal attributes, and ‘‘fair’’ indicated the
presence of a greater number of less
than ideal attributes. A ‘‘poor’’ habitat
quality rating indicated the inferior
conditions of most habitat attributes. Of
total occupied habitat for all BCT
populations, excellent habitat
conditions occurred in approximately
196 km (122 mi) (5 percent); good
conditions occurred in 1,801 km (1,119
mi) (47 percent); fair conditions
occurred in 1,080 km (671 mi) (28
percent); poor conditions occurred in
628 km (390 mi) (16 percent), and
unknown conditions occurred in 126
km (78 mi) (3.2 percent). The majority
of occupied habitat (80 percent) is in
fair, good, or excellent condition.
Livestock grazing occurs in 58 percent
of the BCT populations. Livestock
grazing became an acute problem for
watershed health in the late 1880s
through 1930s when grazing,
particularly sheep grazing, was so
extensive and ill-managed that
widespread watershed damage occurred
throughout many areas in the
Bonneville Basin. In fact, at the turn of
the century, sheep were crowding cattle
out of many areas (Peterson and Speth
1980, p. 179). In the Wasatch Mountains
east of Salt Lake City, Utah, over-grazing
of sheep denuded mountain meadows,
some to the extent that watersheds
experienced massive soil loss, landslides and severe erosional damage. In
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addition to resident sheep, Utah was at
a geographical ‘crossroads of the west’
where hundreds of sheep were trailed to
and from neighboring States (Peterson
and Speth 1980, p. 179).
Overgrazing by sheep can be
particularly damaging to overall
watershed conditions. Sheep have been
known to graze vegetation down to dirt
and ‘‘grub’’ away at grass roots thereby
damaging the soil mantle, which acts to
hold water for plant uptake (Peterson
and Speth 1980, p.180). The extensive
watershed damage typical of overgrazing sheep in the early 20th century
led to massive soil erosion, land slides,
and flooding during heavy precipitation
(Cottam 1947, pp. 23–29). Such events
can completely eliminate local fish
populations and undoubtedly affected
local populations of BCT. For streams
already fragmented from diversions or
dewatering, such events could have led
to local extirpation of BCT where no
connected populations were available to
recolonize streams after a catastrophic
flood.
Although cattle grazing can affect
watershed conditions as well, the
greater concern for cattle grazing stems
from direct stream impacts where cattle
are permitted to dwell in or are trailed
through stream channels and riparian
areas. Without adequate management,
cattle can trample and destroy instream
habitat and stream banks. They forage
on lush riparian vegetation, which leads
to degraded stream conditions and
changes in channel morphology.
Trampling destroys undercut banks
resulting in wider and shallower
channel morphology. Where this occurs,
BCT can be impacted by increased water
temperatures, loss of habitat complexity,
altered macroinvertebrate food-base,
and increased deposition of fine
sediment (Platts 1991, p.393; Belsky et
al. 1999, p.420; Rinne 1999, p.14).
When livestock grazing is managed
appropriately, it can occur in the
vicinity of stream and riparian habitat,
and habitat conditions that support fish
populations can still be maintained
(Fitch and Adams 1998, p. 197). The
Western Watersheds Project, Inc. (Carter
2008, pp. 1–7) submitted information
documenting grazing impacts in
localized areas in the Bear River GMU.
Much of the information documents
range conditions relative to grazing
allotment reauthorizations. The
information and conclusions presented
included the assumption that, if a land
management activity occurred within
the vicinity of a BCT population, it was
adversely affecting the population. We
recognize that overgrazing can cause
adverse impacts to individual
populations of BCT. However, only 16
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percent of the occupied stream miles
have poor habitat quality (May and
Albeke 2005, p. 26). Specific
information on grazing impacts to BCT
habitat on a rangewide basis is not
available. We found no information
indicating that overgrazing significantly
affects the rangewide status of BCT now,
or will do so in the foreseeable future.
Therefore, we conclude that overgrazing
is not a significant threat to BCT.
Roads, timber harvest, and dewatering
occur in the area of some BCT
populations. Similar to water
development and grazing, the greatest
impacts from timber harvesting
occurred from 1850 to 1950. Although
timber harvesting still occurs on
National Forest Lands and very limited
private lands in the Bonneville Basin,
and may have some detrimental impacts
on streams and watersheds, timber
harvesting standards have substantially
improved, particularly regarding
protection of streams and watershed
condition, and the catastrophic
destruction that occurred in the first 100
years of pioneer settlement no longer
occurs.
Currently, timber harvesting affects
BCT through the indirect effects of road
building and deforestation. Road
building is known to add fine sediment
to streams where roads cross or follow
stream channels. These fine sediments
can fill interstitial spaces important for
successful spawning and survival of
eggs and larval fish as well as alter the
macro-invertebrate food base (Williams
and Mundie 1978, p.1032–1033).
Deforestation can also add sediment
input into streams where riparian
buffers are not implemented. Loss of
trees also increases water volume
draining into stream channels, which
can alter flow and sediment regimes or
exacerbate catastrophic flooding during
extreme precipitation events.
Within the Bonneville Basin, timber
harvesting is fairly limited compared to
other areas of the inland west, mainly
because the arid climate is not
conducive to extensive, lush forests.
Timber harvest occurs in only 20
percent of BCT conservation population
habitat (May and Albeke 2005, p. 52,
Table 30). We found no information
indicating that timber harvesting
significantly affects the rangewide status
of BCT now, or will do so in the
foreseeable future. Therefore, we
conclude that timber harvesting is not a
significant threat to BCT.
Direct effects of water diversions and
depletions (dewatering) on BCT occur
where reaches are dewatered or made
inaccessible by instream barriers.
Secondary effects of water development
may include higher water temperatures
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in summer months because of lower
water volume and diminished riparian
condition and altered instream and
shoreline habitat, all of which can
impact cutthroat trout spawning and
populations (Clancy 1988, pp. 40–41).
Dewatering occurs in only 30 percent of
BCT conservation population habitat
(May and Albeke 2005, p. 52, Table 30).
Rates of habitat loss through water
diversions and depletions were likely
heaviest for the decades immediately
after pioneer settlement, in the late
1800s, throughout the Bonneville Basin
near locations of population growth. We
found no information indicating that
dewatering significantly affects the
rangewide status of BCT now, or will do
so in the foreseeable future. Therefore,
we conclude that dewatering is not a
significant threat to BCT.
Idaho and Nevada have no producing
oil or gas wells in BCT areas. However,
oil and gas development has been
accelerating over the last several years
in Utah and Wyoming. Oil and gas
development could affect BCT through
increased land disturbance from roads
and pads that could cause water quality
problems associated with increased
sediment loads, and through leaks,
spills, and discharge of produced water
reaching BCT habitat (WGFD 2004, pp.
25–26). The BLM and Utah Division of
Oil Gas and Mining provided
information on locations of existing
active and inactive wells and oil and gas
leases on BLM, USFS, and other lands
where BLM has jurisdiction over the
subsurface mineral rights within the
BCT range in Utah and Wyoming (BLM
2008a, entire; UDOGM 2008, entire). A
well exists within 1.6 km (1 mi) or less
of 26 BCT conservation populations (17
percent of all conservation populations).
Of these 26 populations, 2 were near
active or producing wells; the wells near
the remaining 24 populations were nonproducing and were shut-in, plugged
and abandoned, or abandoned entirely
for development. These non-producing
wells have a greatly reduced likelihood
of releasing oil and gas related
contaminants into BCT habitat (BLM
2008b, entire). Relatively little overlap
exists between oil and gas development
sites and BCT conservation populations.
BCT populations typically occur at
higher elevations where minimal oil and
gas activity exists. An analysis of
potential future oil and gas development
for the States of Wyoming and Utah
indicates that the majority of leases
occur outside the historic range of BCT
(BLM 2008b, entire). Potential impacts
to BCT resulting from oil and gas
development on Federal land are
typically assessed through the National
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Environmental Policy Act (NEPA)
review process; as a result, future effects
should be disclosed and effects to BCT
will have to be taken into consideration
due to the sensitive species management
status of BCT on Federal land.
Therefore, based on the best scientific
and commercial information available,
we conclude that dewatering is not a
significant threat to BCT now, or in the
foreseeable future.
Summary of Factor A
Land use practices, such as livestock
grazing, road construction and
maintenance, dewatering, and timber
harvest, are occurring to some extent in
most areas of occupied habitat.
However, habitat quality ratings are fair,
good, or excellent in 80 percent of BCT
habitat throughout the current range of
the subspecies. Approximately half of
all BCT populations (49 percent) occur
on Federal lands where land use
regulations are in place to ensure
ongoing maintenance of existing habitat
(see Factor D). Restoration and
conservation activities are occurring for
at least 57 percent of the conservation
populations.
We find that the presence alone of an
activity within a stream segment
containing a conservation population is
not sufficient evidence to conclude that
the population is threatened or that a
certain land use activity affects all
populations rangewide at a significant
level. Additional parameters, such as
magnitude of impacts, distribution and
abundance of BCT populations, and
population trends, lend to an overall
status determination. Many species exist
in managed landscapes; not all are
significantly impacted by human-caused
influences to the level of being
considered threatened under the Act.
BCT conservation populations are
well distributed in four GMUs,
collectively forming a solid basis for
persistence of BCT. These GMUs
contain 19 of the 23 HUCs determined
to have supported historical BCT
habitat. In addition, BCT conservation
populations currently occupy habitat in
three HUCs that are either partially or
totally outside the subspecies’ historic
range.
Based on the best scientific and
commercial information available, we
conclude that BCT is not now or in the
foreseeable future, threatened by
destruction, modification, or
curtailment of its habitat or range to the
extent that listing under the Act as a
threatened or endangered species is
warranted at this time.
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Factor B. Overutilization for
Commercial, Recreational, Scientific, or
Educational Purposes
No commercial harvest of BCT
currently occurs, so only recreational
angling could potentially result in
overutilization. Data show that angling
occurs in 60 percent of BCT
conservation populations (May and
Albeke 2005, p. 52). Utah, Idaho, and
Wyoming have special regulations
providing protection against overharvest of BCT. These special
regulations include catch-and-release
requirements, limited harvest, fishing
closures, and tackle restrictions. In
addition, the remote location of many
BCT streams provides protection from
heavy fishing pressure (NDOW 2006, p.
S–28; Baker et al. 2008, p. 29;
Donaldson 2008, p. 3).
The State of Idaho implements several
fishing regulations to manage potential
angler impacts in State waters. For most
streams able to support larger fish, bag
limits are 2 fish greater than or equal to
40 centimeters (cm) (16 in) in length. In
smaller streams, where BCT typically do
not exceed 30 cm (12 in), the general
stream limit is 2 fish, and no size
constraints exist. In other waters,
seasonal angling restrictions or catchand-release-only regulations are
implemented (IDFG 2008, pp. 3, 19). In
Utah, several fishing regulations protect
native cutthroat trout from
overutilization. The State reduced trout
bag and possession limits from eight
fish to four, and imposed short-term
fishing closures to protect native
cutthroat trout (Donaldson 2008, p. 3).
Wyoming implements angling
restrictions, such as size limits, reduced
bag limits, and tackle restrictions to
protect BCT populations (WGFD 2008,
p. 8). Many of Nevada’s BCT
populations occur in remote areas,
which provide protection from heavy
fishing pressure (Baker et al. 2008, p.
29). None of the four States considers
angling, under their current regulations,
to be a threat to the subspecies.
Collection of BCT for scientific or
educational purposes is controlled by
strict State permitting processes that
prevent excessive sampling throughout
its range in Utah, Wyoming, Idaho, and
Nevada. Collection of fish tissue for
genetic sampling is conducted by
nonlethal techniques (Rogers 2007, pp.
1–3).
Summary of Factor B
No commercial harvest of BCT
currently occurs. Only recreational
angling could potentially result in
overutilization. However, Utah, Idaho,
and Wyoming have special regulations
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providing protection against overharvest of BCT. Also, in our 2001 12month finding (66 FR 51362), we
concluded that angler harvest did not
pose a significant threat to the
continued existence of BCT, and we
know of no new information during
development of this finding to change
this conclusion. Collection of BCT for
scientific or educational purposes is
controlled by strict State permitting
processes throughout the range of the
subspecies. Therefore, we conclude that
the best scientific and commercial
information available indicates that
overutilization for commercial,
recreational, scientific, or educational
purposes is not a significant threat to
BCT now, or in the foreseeable future.
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Factor C. Disease or Predation
Disease
The BCT Conservation Team
evaluated disease in the BCT status
report (May and Albeke 2005, pp. 11–
12, 40–42). Diseases considered had the
potential to cause significant impacts to
population health and included, but
were not limited to, whirling disease,
infectious pancreatic necrosis virus, and
furunculosis. The BCT Conservation
Team assessed risks based on proximity
of disease-causing pathogens and their
accessibility to a population. The
majority of the populations (63 percent)
have limited risk because disease and
pathogens are not known to exist in the
watershed, or a barrier blocks upstream
fish movement. In general, isolated
populations have less risk of
catastrophic diseases. Fourteen
populations (9 percent) are currently
known to be infected with one of the
identified diseases (May and Albeke
2005, pp. 40–41).
In recent years, whirling disease has
become of great concern to fishery
managers in western States. Whirling
disease is caused by the nonnative
myxosporean parasite, Myxobolus
cerebralis. This parasite was introduced
to the United States from Europe in the
1950’s and requires two separate host
organisms to complete its life cycle. Its
essential hosts are a salmonid fish and
an aquatic worm, Tubifex tubifex.
Juvenile, sub-adult, and adult life stages
of BCT have been shown to be
susceptible to whirling disease in the
Logan River, and some Logan River
study sites exhibit a downward trend in
BCT abundance (Budy et al. 2005, pp.
xi-xiii). Despite this, BCT in the Logan
River demonstrate high growth and
survival rates and are generally in
relatively good health. Logan River
tributaries are important refuges from
whirling disease-infected areas in the
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Logan mainstem (Budy et al. 2005, pp.
xi-xiii). Tubifex tubifex is most
abundant in areas of high
sedimentation, warmer water
temperatures, and low dissolved
oxygen. Most populations of BCT occur
in cold water stream habitats at high
elevations, where Tubifex tubifex is less
likely to be abundant.
All four States have developed
management activities to protect BCT
populations from whirling disease.
Though whirling disease is known to
occur in some Nevada waters, it
currently does not pose a threat to BCT
populations because it occurs at low
levels among BCT populations (NDOW
2006, pp. S27). Regardless, Nevada is in
the process of formalizing protocols for
BCT reintroductions and transplants
relating to disease certification and
broodstock management (NDOW 2006,
pp. S27, S32). Idaho has outlined
several strategies to protect BCT
populations from the negative effects of
disease. Strategies include monitoring
fish populations for disease, prohibiting
importation of fish and wildlife that
carry disease risk, and ensuring that
stocking, translocation, and propagation
of fish do not contribute to the
transmission or introduction of diseases
(IDFG 2008, p. 14). Utah has some of the
most stringent fish disease laws in the
United States, which do not allow the
stocking of fish that test positive for
whirling disease (Donaldson 2008, pp.
4–5). UDWR is studying the effects of
whirling disease in a portion of BCT
occupied waters in Utah that have been
infected (Donaldson 2008, p. 4).
Wyoming has a policy of not stocking
fish that test positive for Myxobolus
cerebralis (WGFD 2008, p. 9).
Predation
Of the 153 conservation populations
identified in the rangewide BCT status
report, 97 (63 percent) had no
interaction with nonnative fish and 56
(37 percent) were sympatric with
nonnative fish (May and Albeke 2005, p.
31). All BCT conservation populations
sympatric with nonnative fish are
located in the Bear River and Northern
Bonneville GMUs. In these GMUs, BCT
can be replaced by nonnative trout, but
the degree to which predation is a factor
in this replacement has not been well
documented (Holden et al. 1997, pp. 3–
21). Although nonnative fish can have
negative effects on BCT in localized
areas due to predation, research in the
Logan River drainage shows that it is
possible for BCT populations to persist
in the presence of predacious nonnative
fish (Behnke 1992, p. 107; Budy et al.
2005, pp. xi-xiii).
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Predation can affect BCT, mainly
during early life stages, where other
predaceous fish occupy the same area
(UDWR 2000b, p. 48). Utah has
implemented several management
actions intended to alleviate potential
predation of BCT by nonnative trout,
including: nonnative removal/barrier
installation projects; barring nonnative
cutthroat stocking in conservation
drainages; increasing angler harvest
limits for brook trout in the Boulder and
Uinta Mountains; and initiating
fisheries research work (Donaldson
2008, pp. 5–7). Nevada has virtually
eliminated threats to BCT from
nonnative fish by utilizing barriers and
nonnative removal restoration projects
(Baker et al. 2008, pp. 3–5; NDOW 2006,
p. S–27).
Similar to Utah, Idaho and Wyoming
have enacted management actions
intended to alleviate potential predation
of BCT by nonnative trout. Idaho has
discontinued stocking brook trout into
native trout streams, increased the daily
limit for brook trout from 6 to 25, and
removed or suppressed nonnative trout
species that compete with BCT (IDFG
2008, pp. 6–7). Wyoming is monitoring
BCT populations to ensure that
nonnative populations do not become
established in new waters in the Bear
River drainage, have ceased stocking
nonnative trout in waters managed for
BCT conservation populations, and have
implemented nonnative removal/barrier
installation projects to control
nonnative fish in BCT habitat (Emmrich
2008, p. 2; WGFD 2008, p. 10).
Summary of Factor C
Only 14 (9 percent) BCT conservation
populations are infected with a
significant disease, and no additional
populations are at high risk for infection
(May and Albeke 2005, pp. 40–41).
Therefore, we conclude that the best
scientific and commercial information
available indicates that neither whirling
disease nor other disease organisms
significantly threaten BCT now, or in
the foreseeable future.
Predation by nonnative fish, the
primary source of predation on young
BCT, may have some effect on BCT
populations in the Bear River and
Northern Bonneville GMUs. However,
63 percent of conservation populations
have no interactions with nonnative
fish. Also, research shows that it is
possible for BCT populations to persist
in the presence of predacious nonnative
fish (Behnke 1992, p. 107; Budy et al.
2005, pp. xi–xiii). State fish and wildlife
agencies continue to implement
management actions intended to
alleviate potential predation of BCT by
nonnative fish. At this time, we know of
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no information that indicates to us that
predation significantly affects BCT now,
or in the foreseeable future.
Factor D. Inadequacy of Existing
Regulatory Mechanisms
The Act requires us to examine the
adequacy of existing regulatory
mechanisms with respect to extant
threats that place the subspecies in
danger of becoming either threatened or
endangered. Regulatory mechanisms
affecting BCT fall into three general
categories: angling, land management,
and water quantity.
Angling
The States of Utah, Idaho, Nevada,
and Wyoming consider BCT a game
species, and each State has specific
regulations regarding catching BCT by
angling. We concluded above that
recreational angling is not a significant
threat to BCT, now or in the foreseeable
future (see Factor B).
Regulatory Mechanisms Involving Land
Management
Numerous State and Federal laws and
regulations help reduce adverse effects
of land management activities on BCT.
Most habitat in watersheds inhabited by
BCT conservation populations is
managed by Federal land management
agencies, primarily the USFS and BLM,
and to a limited extent the NPS. Federal
laws that reduce impacts to BCT and
their habitats include the Clean Water
Act, Federal Land Policy and
Management Act, National Forest
Management Act, Wilderness Act, and
National Environmental Policy Act.
Approximately 49 percent of all
occupied BCT habitat (including both
sport fish and conservation populations)
occurs on lands managed by Federal
agencies, and the USFS manages the
majority (May and Albeke 2005, p. 29).
Of the 3,830 km (2,380 mi) of occupied
habitat, 1,867 km (1,160 mi) are under
Federal jurisdiction and the majority
occur on National Forests (1,209 km
(751 miles)) (May and Albeke 2005, p.
29); these figures include sport fish
populations because figures for
conservation populations alone are not
available (see Table 2 below). BCT occur
in a large geographic area within the
following National Forests: BridgerTeton, Caribou-Targhee, Dixie, Fishlake,
Humboldt-Toiyabe, Uinta, and WasatchCache. BCT occupy 11 km (7 mi) of land
administered by the BLM, and 7 km (4.4
mi) managed by the NPS.
Approximately 657 km (408 mi) of
occupied BCT habitat occurs in
wilderness areas managed by the USFS
or BLM. Wilderness Areas and National
Parks provide an extra level of
protection for BCT because many land
management activities are prohibited in
them.
TABLE 2—BCT OCCUPIED LAND OWNERSHIP
[Numbers include areas occupied by both sport fish and conservation populations]
USFS
BLM
1,209 km ..............................................................................
(751 mi) ................................................................................
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U.S. Forest Service
The USFS Sensitive Species Policy in
Forest Manual 2670 outlines procedures
for conserving sensitive species. The
policy applies to projects implemented
under the 1982 National Forest
Management Act (NFMA). The range of
the BCT is within USFS Region 4, where
it is designated a sensitive species by
the USFS, and where the Forests have
Land and Resource Management Plans
(LRMPs) developed under NFMA. The
USFS has proposed a revision to NFMA
in 2008; it is likely that, if the rule is
finalized, LRMPs would be revised
accordingly. The NFMA revision would
result in more strategic and less
prescriptive LRMPs that identify
ecosystem-level desired conditions and
provide management objectives and
guidelines for meeting desired
conditions (Forsgren 2008, pp. 1–2). The
LRMPs might provide species-specific
direction for special status species when
broader, ecosystem-level desired
conditions do not meet conservation
requirements.
USFS Manuals and Handbooks codify
the agency’s policy, practices, and
procedures and are sources of
administrative direction for USFS
employees. USFS Region 4 applies
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NPS
11 km
(7 mi)
7 km
(4.4 mi)
practices outlined in their Soil and
Water Conservation Practices Handbook
to BCT habitat (USFS 1988, pp. 1–71).
This handbook states that the USFS will
apply watershed conservation practices
to sustain healthy soil, riparian, and
aquatic systems. The handbook provides
Management Measures with specific
criteria for implementation. For
example, Management Measure No.
11.01 states: ‘‘The Northern and
Intermountain Regions will manage
watersheds to avoid irreversible effects
on the soil resource and to produce
water of quality and quantity sufficient
to maintain beneficial uses in
compliance with State Water Quality
Standards.’’ Irreversible effects include
reduced natural woody debris, excess
sediment production that could reduce
fish habitat, water temperature and
nutrient increases that could affect
beneficial uses, and compacted or
disturbed soils that could cause site
productivity loss and increased soil
erosion. USFS land management
practices are intended to avoid these
effects whenever possible, while also
providing for multiple-use mandates;
therefore, maintaining or enhancing
BCT habitat is being considered in
conjunction with other agency
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USFS and
BLM
Wilderness
657 km
(408 mi)
Non-federal
2,603 km
(1,618 mi)
Total
3,830 km
(2,380 mi)
priorities. We determined that USFS
BCT management policies are currently
adequately reducing impacts to the
species; we found no information
indicating that threats would rise to a
significant level in the foreseeable
future.
Bureau of Land Management
The BCT is designated a sensitive
species by the BLM in Utah, Wyoming,
Nevada, and Idaho. BLM policy offers
the same level of protection for sensitive
species as for candidate species. The
policy in BLM Manual 6840—Special
Status Species Management (BLM 2001,
pp. 06A3–.06C1), reads as follows: ‘‘For
candidate/sensitive species where lands
administered by the BLM or BLM
authorized actions have a significant
effect on their status, manage the habitat
to conserve the species by:
(a) Ensuring candidate/sensitive
species are appropriately considered in
land use plans.
(b) Developing, cooperating with, and
implementing range-wide or sitespecific management plans,
conservation strategies, and assessments
for candidate/sensitive species that
include specific habitat and population
management objectives designed for
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conservation, as well as management
strategies necessary to meet those
objectives.
(c) Ensuring that BLM activities
affecting the habitat of candidate/
sensitive species are carried out in a
manner that is consistent with
objectives for managing those species.
(d) Monitoring populations and
habitats of candidate/sensitive species
to determine whether management
objectives are being met.’’
BLM land management practices are
intended to avoid negative effects to
species whenever possible, while also
providing for multiple-use mandates;
therefore, maintaining or enhancing
BCT habitat is being considered in
conjunction with other agency
priorities. We find that BLM BCT
management policies are currently
adequately reducing impacts to the
species; we found no information
indicating that threats would rise to a
significant level in the foreseeable
future.
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National Park Service
When the Great Basin National Park
(Park) was established in 1986,
management of southern Snake
Mountain Range streams was transferred
from NDOW and the USFS to the NPS.
The Park developed a Fisheries
Management Plan in 1999 that included
goals of reintroducing BCT into several
area streams. In 1999, 40 km (24 mi) of
stream habitat was unoccupied; due to
restoration activities, 7 BCT
conservation populations now exist in
20 km (12 mi) of streams in and near the
Park (Baker et al. 2008, pp. ii, 1). The
Park will conduct long-term monitoring
on the BCT populations and habitat.
Most BCT waters within the Park are in
remote, high-elevation locations where
angling pressure is very light (Baker et
al. 2008, pp. ii, 1). Livestock grazing,
timber harvest, mining, and
development do not occur in Great
Basin National Park. We find that NPS
management policies are currently
adequately reducing impacts to the
species; we found no information
indicating that threats would rise to a
significant level in the foreseeable
future.
Regulatory Mechanisms Involving Water
Quantity
Utah and Nevada control the
implementation of instream flow
regulations in BCT habitat. In Utah, the
recent legislative session passed an
instream flow bill (HB 117) that should
benefit BCT by allowing private entities,
such as Trout Unlimited, to lease 10year water easements for instream flows
(Donaldson 2008, p. 3). Wyoming has
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approved instream flow rights on 17
stream segments encompassing 66 km
(41 mi) of BCT habitat (WGFD 2008, p.
8). We find that regulatory mechanisms
regarding water policy are currently
adequately protecting the species; we
found no information indicating that
threats would rise to a significant level
in the foreseeable future.
Conservation Actions
State and Federal agencies are
implementing existing programs to
restore and enhance BCT habitat. The
majority of the 153 conservation
populations (57 percent) have one or
more restoration, conservation, or
management activities either completed
or currently being implemented within
BCT habitat (May and Albeke 2005, p.
51). The WGFD adopted a Strategic
Habitat Plan in 2001 (WGFD 2008, p. 6);
under this Plan, habitat biologists work
with landowners and land managers to
manage habitat on a watershed scale to
provide benefits to both terrestrial and
aquatic wildlife resources. The States of
Utah and Nevada have conservation
agreements and conservation strategies
involving review of BCT biology and
monitoring of current subspecies status
and potential threat factors (NDOW
2006, pp. 1 to S–26; UBCTCT 2008, pp.
1–23; UDWR 2008a, pp. 1–41). The
State of Idaho has a Management Plan
for Conservation of BCT in Idaho that
provides conservation direction for BCT
(Teuscher and Capurso 2007, pp. 1–84).
The States of Utah, Nevada,
Wyoming, and Idaho, and the USFS,
BLM, NPS, Service, Confederated Tribes
of the Goshute Reservation, and Utah
Reclamation Mitigation and
Conservation Commission are
signatories to a rangewide conservation
agreement and strategy for BCT. This
agreement was implemented to ensure
the long-term survival of the subspecies
through coordination of conservation
efforts among the signatory agencies
(UDWR 2000b, pp. 1–90).
Numerous conservation actions have
been planned and implemented through
State and Federal conservation and
management plans. For example, the
State of Utah (where the majority of BCT
habitat and conservation populations
exist) submitted two chronologies
detailing BCT conservation efforts over
two different time frames. BCT
conservation actions were grouped from
1973–2001 (approximately 378 actions)
and from 2001–2008 (approximately 355
actions); actions included, for example,
population surveys and monitoring,
genetic analysis, changes to angling
regulations, broodstock development,
fencing of stream habitat, establishment
of conservation easements, nonnative
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fish removal and restocking with BCT,
habitat surveys, stocking policy
changes, and general habitat
enhancement projects (UDWR 2008b,
entire). These chronologies show that
conservation actions were occurring
prior to establishment of the State of
Utah conservation programs in 2000,
and that the number of conservation
activities increased on a yearly basis
(355 within 7 years) once these
programs were enacted. Additionally,
the BCT Conservation Team submitted
information on State and Federal BCT
conservation activities from 2001
through 2007 in Utah, Wyoming, Idaho,
and Nevada; activities are similar to
those of the State of Utah described
above (BCTCT 2008, entire).
Under our Policy for Evaluation of
Conservation Efforts When Making
Listing Decisions (PECE) (68 FR 15100;
March 28, 2003), we typically evaluate
conservation efforts by State and local
governments, and other entities, that
have been planned but not
implemented, or implemented but have
not yet demonstrated effectiveness, in
order to determine which efforts meet
the standard in PECE for contributing to
our finding. The actions described
above were not analyzed using the PECE
standard because they were
implemented prior to this review and
their effectiveness has been
demonstrated by the general increases
in BCT population numbers (as
discussed in the BCT Population Trend
section). State and Federal agency
participation in BCT conservation plans
is voluntary; however, the States
included in the range of the BCT have
a demonstrated history of effective
management of the species. State plans
are typically in place indefinitely or
have a term of agreement for 5–10 years
with renewal provisions for a similar
time period. The rangewide BCT
conservation agreement was renewed in
2008 for 10 years, with the commitment
that it would be extended for an
additional 10 years upon expiration.
The success of the conservation actions,
as explained above, indicates that
participating State and Federal agencies
are committed to the conservation of
BCT, and the renewal of the rangewide
BCT agreement gives us a reasonable
expectation that these efforts will
continue in the foreseeable future.
Summary of Factor D
We assessed the potential threats of
livestock grazing, timber harvest, roads,
water management, mining, oil and gas
developments, angling, disease, and
predation with regard to magnitude of
impacts to BCT, and to whether
regulatory mechanisms are adequate.
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We find that regulatory mechanisms
related to land and fisheries
management are currently sufficient for
mitigating potential threats to BCT, and
that the stable status of the species will
continue in the foreseeable future. The
best scientific and commercial
information available indicates that
existing regulatory mechanisms have
maintained or improved the status of
BCT to the extent that listing under the
Act as a threatened or endangered
species is not warranted.
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Factor E. Other Natural or Manmade
Factors Affecting the Species’ Continued
Existence
Climate Change
The Intergovernmental Panel on
Climate Change (IPCC) has concluded
that warming of climate is unequivocal
(2007, p. 5), and that temperature
increase is widespread over the globe
and is greater at higher northern
latitudes (IPCC 2007, p. 30). However,
future changes in temperature and
precipitation will vary regionally and
locally, with some areas remaining
unaffected or even decreasing in
temperature (IPCC 2007, pp. 46–47).
Changes in precipitation are less certain
than in temperature; climate models
project more frequent heavy
precipitation events, separated by longer
dry spells, especially in Utah and the
western United States (GBRAC 2007, p.
A1, 14–15; IPCC 2007, p. 15).
During the past decade, the average
temperature in Utah, like that of much
of the globe, was higher than observed
during any comparable period of the
past century (IPCC 2007, pp. 31–32). As
discussed below, that increase in
temperature, if permanent, does not
constitute a significant threat to the
BCT. The remaining question is whether
possible future increases in temperature
will constitute a threat. Over the next 20
years, climate models estimate that the
Earth’s average surface temperature will
increase about 1.4 °C (0.8 °F). Climate
change predictions based on
continental-scale analysis are generally
given ranking based on degree of
certainty (IPCC 2007, p. 27; GBRAC
2007, pp. 3–11). Utah is projected to
warm more than the global average
(GBRAC 2007, pp. ES 2–3); however,
levels of confidence in projections for
local-scale areas are lower than for
projections at global or continental
scales, and are generally not given a
degree of certainty ranking (GBRAC
2007, pp. 17–20). Clear and robust
future trends have not been developed
for Utah (GBRAC 2007, p. 2). We cannot
make reliable predictions about the
magnitude or timing of future
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temperature increases within the range
of the BCT.
Based on the Utah Governor’s Blue
Ribbon Advisory Council on Climate
Change (2007), which is a regional
study, climate change will likely cause
environmental changes in Utah, which
could increase challenges for BCT
rangewide. According to some research,
climate change has already had or is
predicted to have negative
consequences on coldwater fisheries
globally (Nakano et al. 1996, p. 711;
Hari et al. 2006, p. 24), and in the
Southwest and Rocky Mountains of
North America (Keleher and Rahel 1996,
p. 1; Rahel et al. 1996, pp. 101, 102,
113), through increases in ground- and
surface-water temperatures. Rahel et al.
(1996, p. 1116) and Keleher and Rahel
(1996, p. 9) predicted that elevationally
diverse regions such as the Rocky
Mountains will experience warming
stream temperatures that could restrict
cold water species, such as cutthroat
trout, to increasingly higher elevations,
thus reducing the geographic range and
occupied stream distance and increasing
habitat fragmentation. Keleher and
Rahel (1996, p. 5) calculated that in
Wyoming a 1 °C (1.8 °F) increase in
mean July air temperatures could
decrease the length of streams
inhabitable by salmonid fish by 8
percent; a 2 °C (3.6 °F) increase could
cause a reduction of 14 percent, a 3 °C
(5.4 °F) increase could cause a 21
percent decline, a 4 °C (7.2 °F) increase
could cause a 31 percent reduction, and
a 5 °C (9 °F) increase could cause a 43
percent reduction. In the Rocky
Mountains, Keleher and Rahel (1996, p.
5) calculated similarly high reductions
of 16.8, 35.6, 49.8, 62.0, and 71.8
percent with respective temperature
increases of 1, 2, 3, 4, or 5 °C in July
air temperatures. One study concluded
that if warming air temperatures occur,
it will likely cause numerous
fundamental environmental changes,
including increased stream and lake
temperatures, increased evaporation
rates, reduced annual snowpack,
changes in river flows, and increases in
disturbance events such as floods,
drought, and fire (Williams et al. 2007,
p. 2).
However, even if temperatures within
the range of the BCT increased by the
amounts considered in these studies, it
would not put the species in danger of
extinction. Bonneville cutthroat trout
may be able to sustain viable
populations at slightly warmer
temperature conditions than other
cutthroat trout subspecies. For example,
Williams et al. (2007, p. 3) reported that
less than 1 percent of the total
distribution of westslope cutthroat trout
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and Colorado River cutthroat trout
occurred in streams with an average July
temperature greater than 22 °C (71.6 °F),
but nearly 20 percent of the historical
distribution of Bonneville cutthroat
trout was associated with a mean July
air temperature greater than 22 °C (71.6
°F). In addition, Bonneville cutthroat
trout appeared to be thermally
distributed bimodally, with two peaks.
The warmer second peak occurred due
to an extensive network of lower
elevation, warmer valley bottoms that
were historically occupied (Williams et
al. 2007, p. 3). Bonneville cutthroat
trout have adapted to a broad spectrum
of habitat conditions throughout their
range (Kershner 1995, p. 28).
Water temperature increases could
result in a potential benefit to
Bonneville cutthroat trout in localized
areas. Cold summer water temperatures
(mean July temperature of less than 7.8
°C (46 °F)) have been found as a limiting
factor to recruitment of cutthroat trout
in high-elevation streams (Harig and
Fausch 2002, p. 545; Coleman and
Fausch 2007, pp. 1238–1240).
Therefore, although climate change is
likely to increase water temperatures
and result in a reduction in habitat
quality for lower elevation streams,
some higher elevation streams may
become more suitable for BCT.
Declines in low-elevation mountain
snowpack have been observed over the
past several decades in the Pacific
Northwest and California. However, no
clear long-term snowpack trends are
currently evident in Utah’s mountains
(Hamlet et al. 2005, p. 4560; GBRAC
2007, pp. A1, 1–2). Dates of peak snow
accumulation and peak melt have also
been trending earlier, but with the most
notable differences occurring in coastal
areas of the West that have warmer
winter temperatures (Hamlet et al. 2005,
p. 4560). Stewart et al. (2005, p. 1152)
indicate that spring streamflow in the
western United States during the last 5
decades has shifted so that the major
peak now arrives 1 to 4 weeks earlier,
resulting in declining fractions of flow
in the spring and summer. However,
streamflows in Utah and the
Intermountain West do not show clear
trends over the past 50 years (GBRAC
2007, p. A1, 10).
In another study, three elements of
environmental change expected to affect
Western cutthroat trout as a result of
climate change (increased summer
water temperatures, flood events, and
wildfire) were modeled to determine
where a particular subspecies is likely
to be at greatest risk (Williams et al.
2007, pp. 2–5). The three elements were
modeled individually, and then
combined into a composite risk and
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modeled jointly. Modeling showed that
43 percent of sub-watersheds with
existing BCT populations are at low or
moderate risk from climate change, and
57 percent are at high risk. The
modeling also evaluated BCT
populations in regional areas. The
composite analysis showed that
cutthroat populations in most of the
Bear River basin and the eastern portion
of the Northern Bonneville basins are
likely at low risk from climate change,
while the West Desert, Southern
Bonneville, and Northern Bonneville
basins are in the moderate to high-risk
range (Williams et al. 2007, p. 6).
A recent status review (73 FR 27899;
May 14, 2008) for the Rio Grande
cutthroat trout (Oncorhynchus clarkii
virginalis) provided a comprehensive
review of potential global and regional
climate change effects to that
subspecies. The status review provided
detailed information regarding the
potential effects of temperature change,
decreased stream flow, change in
hydrograph, and increases in extreme
events.
The Rio Grande cutthroat trout is
native to the Rio Grande, Pecos, and
Canadian River basins in New Mexico
and Colorado (Behnke 2002, p. 219); the
northern extent of this subspecies’ range
lies at a more southerly latitude than the
range of the Bonneville cutthroat trout.
Therefore, predictions of the effects of
climate change are likely to differ to
some extent between the subspecies.
One of the effects of climate change is
that salmonid species are likely to be
restricted to increasingly higher
elevations or to more northern latitudes
(Meisner et al. 1988, p. 6; Regier and
Meisner 1990, p.11; Keleher and Rahel
1996, p. 2; Nakano et al. 1996, pp. 716,
717; Rahel et al. 1996, p. 1122; Poff et
al. 2002, p. 7; Rieman et al. 2007, p.
1558). Coldwater species occupying the
southern distributions of their range,
such as the Rio Grande cutthroat trout,
are seen as more susceptible to
extirpation as a consequence of global
climate change (Poff et al. 2002, p. 8;
Rieman et al. 2007, pp. 1552, 1553).
Because Rio Grande cutthroat trout
primarily occupy high-elevation
headwater tributaries, dispersal to new
habitats is unlikely because they
currently occupy the uppermost
available habitat (73 FR 27899; May 14,
2008). In contrast, habitat for the
Bonneville cutthroat trout is widely
distributed and variable, ranging from
high-elevation (3,500 m mean sea level)
streams with coniferous and deciduous
riparian trees to low-elevation (1,000 m
mean sea level) streams in sage-steppe
grasslands containing herbaceous
riparian zones (Kerschner 1995; p. 28).
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BCT have adapted in order to survive in
relatively warm water and marginal
habitats, and migratory life forms
historically grew to be quite large in
lakes and large rivers. Some populations
within the Bear River drainage in
southern Idaho and northern Utah
continue to exhibit the species’
impressive range of life history
strategies and habitat requirements,
migrating seasonally between turbid,
lower elevation mainstem rivers and
cold, clear, high-elevation tributary
streams (Trout Unlimited 2008, entire).
Climate change biological projections
are based on effects models that have
varying degrees of uncertainty (IPCC
2002, pp. 14–16). For example, Williams
et al. (2007, p. 6), in their modeling of
climate change and western trout, used
a 3 °C temperature increase (projected
for the U.S. Pacific Northwest in this
century based on a 2004 University of
Washington Climate Impacts Group). It
is unknown when the predicted 3 °C
raise in temperature might be realized.
Questions also remain regarding the
projected extent of climate change
across regional areas, the timeframe for
temperature and precipitation changes,
and the overall response of fish
populations. It is unclear how climate
change will interact with other
environmental stressors at regional
levels (IPCC 2002, p. 15).
While climate change is likely to
affect aquatic resources to some extent,
including habitat utilized by BCT, at
this time we find that these effects are
not likely to cause significant long-term
impacts to population viability. Current
data indicate that the observed recent
effects of climate change have had little
significant impact on BCT population
trends. BCT population trends show
increasing numbers of conservation
populations and increases in the
amount of occupied river habitat, from
15 populations in 34 km (21 mi) of
habitat in 1978, to 153 populations in
3,316 km (2,061 mi) in 2004 (May and
Albeke 2005, p. 31; Hickman 1978, pp.
121–122). Therefore, although climate
change may cause some level of longterm effects to aquatic habitat, we find
that climate change is not currently a
threat to BCT, which have adapted to a
broad spectrum of habitat conditions.
We also find that climate change is not
likely to significantly threaten the
species rangewide within the
foreseeable future.
Fragmentation and Isolation of Small
BCT Populations in Headwater Areas
The majority of BCT conservation
populations (101; 66 percent) occur as
isolated, non-networked populations
(May and Albeke 2005, p. 34); 25
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populations (16 percent) are weakly
connected; 15 populations (10 percent)
are moderately connected; and 12
populations (8 percent) have migratory
forms and open migration corridors that
make them strongly connected. The
strongly connected populations occur in
Utah, Idaho, and Wyoming in the Bear
River and Northern Bonneville GMUs
(May and Albeke 2005, pp. 34, 107, 115,
117).
Cutthroat metapopulations are
defined as a collection of localized
populations that are geographically
distinct but genetically interconnected
through natural movement of individual
fish between populations (UDWR 2000a,
p. 8). Metapopulations are important
because they maintain genetic exchange
and increase genetic diversity. They also
provide individuals to repopulate
stream segments where populations are
lost due to stochastic environmental
events. Metapopulations are important
to the overall status of the subspecies,
but they are at a higher risk for disease
and invasion of nonnative fish because
these elements can move into any
connected populations even if they are
introduced into a single localized area.
Problems associated with small,
isolated cutthroat trout populations
include increased risk of extirpation by
catastrophic events and loss of genetic
exchange. Isolated populations can also
potentially be at risk of extirpation due
to ongoing environmental forces causing
changes in attributes such as habitat
size, pool availability, or water
temperatures. Several researchers have
attempted to determine which
environmental factors contribute to
successful translocation efforts intended
to augment isolated populations, and to
integrate environmental factors into
assessments of stream viability for
cutthroat trout. Cold summer water
temperature, narrow stream widths, and
lack of deep pools can limit successful
translocations of cutthroat trout (Harig
and Fausch 2002, pp. 545–547). In highelevation streams, cold summer water
temperatures can delay spawning and
lack of deep-water pools can limit
overwinter survival. Modeling of these
stream variables indicates that occupied
stream length is an even better predictor
of cutthroat trout abundance than
stream temperatures; small increases in
habitat length (e.g., by barrier removal
or rewetting of a dewatered stream
segment) can produce a
disproportionately greater increase in
fish abundance, increasing viability of
isolated populations (Young et al. 2005,
pp. 2405–2406).
A static model intended to describe
the relationship between fish abundance
and habitat is a tool for managers
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implementing cutthroat trout restoration
projects (Hildebrand and Kershner 2000,
pp. 515–518). The model is especially
useful in evaluating potential
installation of artificial barriers to
protect from nonnative fish invasion.
Modeling indicated that a stream length
of 3 km (2 mi) is required to support a
population of 1,000 fish; 8 km (5 mi)
supports 2,500 fish; and 17 km (10 mi)
supports 5,000 fish. The model is not
applicable in all situations; it
incorporates several assumptions
specifying that it is most relevant to
isolated populations in streams less
than 7 meters wide, and that food
availability and habitat quality affect the
relationship between fish abundance
and stream length occupied. The
relevance of the model for
reintroduction and restoration of BCT
populations should be carefully
assessed, as small, isolated cutthroat
trout populations have persisted for
many years, e.g., above waterfalls or in
desert basins. Lack of habitat to sustain
a large population does not necessarily
mean that a population is destined to go
extinct (Hilderbrand and Kershner 2000,
p. 517). Specific criteria for viable
population size has not been developed
for BCT.
Small, isolated populations are at
greater risk from stochastic events such
as fire, floods, and drought. However,
the widespread geographic distribution
of BCT conservation populations in
numerous individual populations
mitigates the potential of future
catastrophic natural events to affect a
large proportion of the populations. It is
unlikely that a sufficient number of
populations would be lost to affect the
overall status of the subspecies.
Fisheries management agencies have
the ability to maintain or reestablish
BCT populations in areas where they are
partially impacted or lost to natural
catastrophic events. While not to be
relied on for species conservation,
restoration and reintroduction can be
employed as tools in specific cases. For
example, wildfire can present an
opportunity to eliminate nonnative
fishes that occur in BCT habitat, after
which reestablishment of BCT can
occur. BCT populations have been
established in burned-over streams
previously only occupied by nonnative
trout, including Leeds Creek and South
Ash Creek in the Pine Valley
Mountains, and Birch Creek, a tributary
to the Sevier River (Ottenbacher 2008,
entire).
Active programs are in place to
restore metapopulations, where
possible, within the historic range of
BCT in Utah and Nevada (Donaldson
2008, pp. 9–10; NDOW 2006, p. S–8).
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All GMUs currently have networked
populations (metapopulations), and the
strongest and largest networks occur in
the Bear River and Northern Bonneville
GMUs (May and Albeke 2005, p. 34).
A population health evaluation was
conducted for all BCT conservation
populations, based on four health
indicators: Temporal variability (based
on stream length), population size,
population production potential (growth
and survival rates), and population
connectivity (May and Albeke 2005, pp.
44–49). The health evaluation indicated
that 91 conservation populations (59
percent) occur in stream reaches of less
than 10 km (6 mi) (May and Albeke
2005, pp. 44–49). Approximately 38
conservation populations (25 percent)
occupy stream reaches between 10 km
(6 mi) and 31 km (19 mi), and 24
populations (16 percent) occupy stream
reaches of 32 km (20 mi) or more.
Conservation populations include: 32
percent with at least 2,000 adult BCT;
25 percent with between 500 and 2,000
adult BCT; 22 percent with between 50
and 500 adult BCT; and 21 percent with
fewer than 50 adult BCT.
Most of the conservation populations
(81 percent) were moderately healthy in
terms of growth and survival
(population production potential), based
on habitat quality, presence of
nonnative trout, disease risk, land uses,
and recovery actions. Composite scores
of conservation population general
health included: 7 percent high; 39
percent moderately high; 37 percent
moderately low; and 17 percent low
(May and Albeke 2005, pp. 44–49). Low
to moderately low composite scores (54
percent of BCT conservation
populations) were primarily a result of
the number of small, isolated
populations. Even though most
populations (66 percent) are small and
isolated, these populations are found in
a minority of the total BCT conservation
population habitat; 70 percent of total
habitat has BCT conservation
populations that are moderately or
strongly connected. As is explained
below, these isolated populations have
been incorporated into the BCT
Conservation Team’s conservation
strategies and allow for BCT
conservation populations that are less
susceptible to introgression, disease,
and competition from nonnative fish.
The BCT Conservation Team
developed two conservation strategies
for BCT conservation and management
(May and Albeke 2005, p. iii). One
strategy emphasizes isolated
populations because they are less
susceptible to introgression, disease,
and competition from nonnative fish. In
addition, multiple populations
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distributed throughout a watershed
reduce risk because the simultaneous
loss of all populations within the
watershed is unlikely. The other
strategy emphasizes preserving and
restoring metapopulations to provide
genetic exchange and allow for larger
populations. Within the current range of
BCT, and within each GMU, both
isolated populations and
metapopulations are present, providing
for success of both conservation
strategies.
The best available information
indicates that, while most BCT
conservation populations occur in small
stream reaches (59 percent), most have
moderately healthy growth and survival
rates (54 percent). In addition, 70
percent of total habitat includes
populations that are moderately or
strongly connected. Therefore, we find
that BCT conservation populations are
adequately healthy and will remain so
in the foreseeable future.
Nonnative Fishes
Introduced nonnative fish are a
potential threat to native cutthroat
subspecies (UDWR 2000a, pp. 1–9; May
and Albeke 2005, pp. 21–24). We
address this potential threat factor by
breaking it into three components: (1)
Management practices that included
stocking of nonnative fish; (2)
competition of nonnative fish with BCT;
and (3) hybridization of BCT with
nonnative fish. We summarize all three
of these components together in the
summary of Factor E because they are
interrelated.
Fisheries Management
Since the late 1800s, early pioneers
and fisheries managers have
implemented fish stocking programs
that introduced nonnative salmonids
into lake and stream habitats of BCT.
Brook trout were introduced into waters
in Utah as early as 1875, rainbow trout
in 1883, and brown trout (Salmo trutta)
possibly as early as 1895 (Popov and
Low 1950, pp. 49–57; Sigler and Miller
1963, pp. 29–54). It is unknown exactly
when nonnative cutthroat were
introduced; in 1899, 11,000 adults and
yearling cutthroat trout were sent to the
Fish and Game Warden in Salt Lake City
(Ravenel 1900, pp. 35–118). This
delivery may have included several
subspecies, including Yellowstone
cutthroat trout (Sigler and Miller 1963,
pp. 29–54). The earliest stocking records
indicate large numbers of young
nonnative fish were stocked for decades
into accessible waters in an effort to
restore or sustain a high-quality fishery
(Holden et al. 1997, pp. 2–1 to 2–13).
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In 1915, nearly 2 million cutthroat
and more than 7 million other trout
were planted in Utah waters alone
within the Bonneville Basin (Cope 1955,
pp. 89–93). Of the cutthroat stocked in
1915, 100,000 were from Utah, and the
remainder were collected from Bear
Lake and other productive cutthroat
populations and stocked into less
productive or exploited systems. From
1915 to 1952, more than 100 million
cutthroat were planted, comprising
about one-third of the total stocking
effort in Utah; approximately 45 percent
were imported from Utah, almost
exclusively from Yellowstone Lake
(Cope 1955, pp. 89–93, as reported from
biennial Utah State Fish and Game
Commission reports 1915–1952).
Comprehensive stocking records from
the turn of the century for the
Bonneville Basin in Nevada, Idaho, and
Wyoming are not readily available
because most of these peripheral areas
of the Bonneville Basin are remote and
inaccessible. However, it has been
suggested that settlers moved fish
among drainages in remote areas like
the Snake Valley and the Pine Valley
Mountains in the mid-to late-1800s
(Miller and Alcorn 1946, pp. 173 193;
Popov and Low 1950, pp. 38–39;
Behnke 1992, pp. 134–135). Fish
transplanting among and across
drainages, without oversight, consent, or
record-keeping, was likely common in
remote pioneer settlements.
Although many nonnative species
were once stocked throughout Utah,
salmonid species, particularly rainbow
trout, Yellowstone cutthroat trout, and
brook trout, comprise the greatest
potential threat to BCT. Rainbow and
Yellowstone cutthroat trout can
interbreed with BCT (Busack and Gall
1981, pp. 948–950; Weigel et al. 2002,
pp. 397–401), and brook trout can be a
competitor for food sources (Peterson et
al. 2004, p. 769) (see next section on
Competition). Rainbow trout were
regularly stocked into most cold, clearwater stream systems and
impoundments throughout the
Bonneville Basin (Duff 1988, pp. 121–
127; Holden et al. 1997, pp. 2–5 to 2–
13). Rainbow trout were commonly
stocked at accessible sites, which was
not always successful in establishing
wild populations (those that naturally
reproduce and recruit in the wild). As
a result, annual stocking was necessary
to maintain a sustainable fishery. Heavy
annual stocking has taken place in some
streams for more than a century. In the
past 30 years, stocking was modified to
prevent introduction of nonnative
salmonids into waters with known pure
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populations of BCT in Utah (Holden et
al. 1997, pp. 2–13 to 2–22).
Because of the nearby source of fry in
Yellowstone Lake, Yellowstone
cutthroat trout were readily available for
stocking. Yellowstone and other
subspecies of cutthroat trout were
stocked into streams to supplement the
declining native fishery. In some cases,
(e.g., Bear Lake) substantial records exist
of annual stocking of Yellowstone
cutthroat trout and other species.
Despite this stocking, Yellowstone
cutthroat trout did not necessarily
become established in all waters into
which they were stocked, and BCT in
some areas have resisted hybridization
with and replacement by nonnative
trout (e.g., Bear Lake) (Behnke 1992, p
137). Genetic information is not
currently sufficient to clearly discern
Yellowstone cutthroat trout from BCT in
the Bear River drainage because of their
recent evolutionary divergence;
however, morphological characteristics
are distinctive between BCT and
Yellowstone cutthroat trout and can be
used to determine hybridization where
it is suspected (Behnke 1992, pp. 132–
138; Shiozawa 2008, p. 1).
State fish and wildlife agencies no
longer stock nonnative trout in BCT
habitat, and are implementing strategies
to minimize impacts to BCT from
nonnatives, such as installing fish
barriers, removing nonnative fish, and
increasing nonnative fish bag limits.
Competition From Nonnative Fish
Nonnative trout are known to
compete with BCT (Behnke 1992, p. 54).
Brown trout can successfully compete
with BCT (Budy et al. 2005, pp. xi–xiii),
and brook trout can displace cutthroat
trout when they occur in the same
habitat (Peterson et al. 2004, p. 769).
Nonnative fish are sympatric with BCT
within currently occupied habitat in the
four GMUs (May and Albeke 2005, pp.
27–28). Currently occupied BCT habitat
includes 37 percent (1,365 km/848 mi)
without nonnative fish, and 63 percent
(2,466 km/1,532 mi) with nonnative
fish. The majority of habitat with
nonnative fish is in the Bear River
(1,398 km/869 mi) and Northern
Bonneville (1,024 km/636 mi) GMUs.
Only 45 km (28 mi) in the Southern
Bonneville GMU have nonnative fish.
No nonnative fish exist within the West
Desert GMU in BCT conservation
population habitat.
BCT conservation populations
represent approximately 87 percent of
currently occupied habitat (the other 13
percent includes sport fish) (May and
Albeke 2005, p. 31). Of the 153 BCT
conservation populations, 97 (63
percent) have no interaction with
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nonnative fish, and 56 (37 percent) are
sympatric with nonnative fish (May and
Albeke 2005, p. 31).
Natural and human-made barriers
protect some BCT populations from
competition with nonnative fish.
Rangewide, barriers assist in protecting
35 BCT conservation populations
occupying 480 km (298 mi) of stream
(Burnett 2008b, pp. 1– Barriers help
protect populations from nonnative fish
invasion, but negative effects, such as
blocking fish movement and
fragmenting habitat, should be assessed
and balanced before installing barriers.
Therefore, this strategy for managing
nonnative fish is not appropriate for all
native cutthroat populations.
Hybridization With Nonnative Fishes
The scientific criteria for describing
and formally recognizing taxonomic
species of fish are based almost entirely
on morphological characters (Behnke
1992, pp. 7–11). The advent of
molecular genetic techniques in the
mid-1960s added an additional set of
biological markers that are used to
distinguish species and subspecies of
native trout in the western United
States. Most genetic analyses on native
cutthroat trout have confirmed the
evolutionary distinctness among species
and subspecies that had been described
taxonomically on the basis of
morphology (Behnke 1992, pp. 7–11).
Cutthroat trout populations that are
less than 10 percent introgressed with
nonnative species (or other cutthroat
subspecies) retain morphological,
behavioral, and ecological
characteristics of their nonintrogressed
ancestors (UDWR 2000a, pp. 1–9).
Individuals of a particular cutthroat
trout subspecies can possess nuclear
genes from another taxon, detectable
only by molecular genetic techniques,
while still conforming morphologically,
behaviorally, and ecologically to the
scientific taxonomic description of the
parental native species (Busack and Gall
1981, pp. 948–950; Weigel et al. 2002,
pp. 397–401).
We do not consider populations or
individual fish conforming
morphologically to the scientific
taxonomic description of BCT to be a
hybridization threat to BCT. Although
such individuals may have a low
frequency of genes from another taxon
(less than 10 percent), we have found no
information indicating that such
individuals express behavioral,
ecological, or life-history characteristics
differently than BCT native to a
particular geographic area. The
frequency of genes from other taxons
will likely remain low in BCT
populations for several reasons: (1) In
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some locations BCT likely can have an
ecological advantage over nonnative fish
because they have adapted over long
time periods to their specific habitat; (2)
stocking of nonnative trout in BCT
habitat is no longer practiced by fish
and wildlife agencies; and (3) 61 percent
of BCT conservation populations are
isolated by human-caused or natural
barriers, protecting them from
increasing numbers of nonnative trout
(May and Albeke 2005, p. 37).
Some introgressed populations may
be valuable to the overall conservation
and survival of a species or subspecies
(Campton and Kaeding 2005, pp. 1323–
1324; USFWS 2003, pp. 46992–46993),
because they can still express important
behavioral, life history, or ecological
adaptations of the indigenous
population within a particular
geographic area. BCT have evolved in
varying environmental conditions in
differing habitats across its range, and
these conditions have likely influenced
its behavioral and life history traits. For
example, BCT with fluvial and adfluvial
life-history strategies migrate up small
streams to spawn, and BCT with a
resident life-history strategy are able to
conduct their entire life history
(spawning, nursery/rearing, adult stage
including overwintering) in headwater
tributaries that provide all necessary
life-history habitat types. Environmental
conditions particular to a specific BCT
population’s ecological setting (e.g.,
latitude, elevation, temperature and
precipitation regime) may allow for
development of locally adapted traits
that would justify preservation of a
partially introgressed population.
Maintaining unique life-history traits
can outweigh the negative aspects of
limited introgression. Thus, agencies
should carefully evaluate the long-term
conservation implications of strategies
for managing introgressed BCT
populations within the range of the BCT
(USFWS 2003, pp. 46992–46993;
Campton and Kaeding 2005, pp. 1323–
1324), as different strategies may be
appropriate for different populations.
No standards exist that define exact
thresholds for acceptable levels of
hybridization in cutthroat trout;
however, we assessed all relevant
scientific and commercial information
available in order to arrive at generally
applicable standards. These standards
are applicable to other species of
cutthroat trout we have assessed,
including the Yellowstone (71 FR 8818,
February 21, 2006) and Colorado River
(72 FR 32589, June 13, 2007) cutthroat
trout subspecies. Similar standards were
applied to the Westslope cutthroat trout
(WCT) (68 FR 46989, August 7, 2003);
however, specific research was
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conducted indicating that WCT 20percent introgressed with rainbow trout
were indistinguishable morphologically
from nonintrogressed WCT (Weigel et
al. 2002, pp.397–401). Species-specific
research comparing morphological
characteristics to genetic introgression
thresholds has not been conducted on
other cutthroat subspecies; therefore, we
used the more conservative threshold of
10 percent to define BCT conservation
populations.
When BCT are sympatric with
rainbow trout and nonnative subspecies
of cutthroat trout, introgressed
populations can occur, and because of
this, researchers have studied the
genetic status of BCT. These studies
have measured levels of introgression in
the BCT in targeted areas of its range,
but have not, additionally, measured the
morphological characteristics present at
varying levels of introgression. The
rangewide status report includes a
summary of BCT genetic status (May
and Albeke 2005, pp. 21–24).
Genetic testing was conducted in
more than 784 km (487 mi) of BCT
occupied habitats (20 percent of
occupied habitat) (May and Albeke
2005, pp. 21–24). This research was
conducted specifically in populations
that appeared to be typical of the BCT
phenotype; while results help elucidate
the level of introgression in BCT, they
cannot be used to summarize rangewide
introgression levels. Test results showed
no evidence of introgression in samples
from 611 km (411 mi) of occupied
habitat (17 percent of occupied habitat).
An additional 1,215 km (755 mi) of
occupied habitat (32 percent of
occupied habitat) has populations
suspected to be genetically unaltered,
based on the absence of introduced
hybridizing species and of stocking
records for hybridizing species. The
BCT Coordination Team has classified
these as conservation populations.
Hybridized fish occur in approximately
122 km (76 mi) of stream habitat
(4 percent of occupied habitat). An
additional 1,831 km (1,138 mi) of
habitat (48 percent of occupied habitat)
contains fish that are potentially
hybridized, based on the presence of
nonnative hybridizing species or
records indicating past stocking of
nonnative hybridizing species.
Researchers also assessed the genetic
contamination risk, based on proximity
and accessibility of rainbow trout and
nonnative cutthroat trout, for the 153
BCT conservation populations (May and
Albeke 2005, p. 37). A low genetic risk
was found in BCT populations (94
populations; 61 percent) where a barrier
provides complete blockage to upstream
fish movement of introduced
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hybridizing species. A moderately low
genetic risk was found in BCT
populations greater than 10 km (6 mi)
from hybridizing species or subspecies,
and a moderately high risk was found in
BCT populations within 10 km (6 mi) of
hybridizing species or subspecies (27
populations; 18 percent). A high risk
rating was found in BCT populations
(32 populations; 21 percent) sympatric
with hybridizing species in the same
stream segment. Of the populations that
were rated with low risk of genetic
contamination, 87 (93 percent) were
identified as being isolated populations.
Summary of Nonnative Fishes
Despite the presence of nonnative fish
species sympatric with BCT, we find
that stocking, competition, and
hybridization do not pose significant
threats to BCT, because: (1) In some
locations BCT likely can have an
ecological advantage over nonnative fish
because they have adapted over long
time periods to their habitat; (2) welldistributed core populations of BCT
persist in streams with nonnative fish;
(3) 61 percent of BCT populations are
isolated from nonnative fish by natural
or constructed barriers; and (4) stocking
of nonnative fish no longer occurs in
waters with BCT conservation
populations. In addition, programs are
being implemented to remove nonnative
trout, through mechanical or chemical
means, from BCT waters in all four
States (NDOW 2006, p. S–22; IDFG
2008, pp. 9–10; Donaldson 2008, p. 5;
WGFD 2008, p. 10). In Utah, between
2001 and 2007, nonnative fish removal
was conducted on more than 80 km
(50 mi) of BCT streams (Donaldson
2008, p. 5).
Groundwater Pumping
Multiple filings for groundwater
withdrawal from both the carbonaterock and alluvial aquifers in the Great
Basin are currently in place within the
historic range of BCT populations in the
West Desert GMU. Southern Nevada
Water Authority (SNWA) has applied to
the BLM for issuance of rights-of-way to
construct and operate a system of
regional water supply and conveyance
facilities. The project would include
conveyance of up to 24,384 hectares per
meter (ha-m) (200,000 acre-feet per year
(ac-ft)) of groundwater—20,360 ha-m
(167,000 ac-ft) by SNWA with the
remaining capacity provided for Lincoln
County Water District from six
hydrographic basins (SNWA 2007, p. 1–
1). The groundwater that SNWA intends
to convey would be from both existing
and future permitted water rights in
hydrographic basins of the Great Salt
Lake Desert Regional Flow System
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(Nevada and Utah) and White River
Flow System (Nevada).
SNWA’s Groundwater Development
(GWD) Project includes construction
and operation of groundwater
production wells, water conveyance
facilities, and power facilities. The
proposed production wells and facilities
would be located on public lands
managed by BLM in Nevada. No
facilities are planned in Utah (SNWA
2007, p. 1–1).
The Nevada State Engineer issued a
ruling on April 16, 2007, approving a
major portion of the SNWA
groundwater rights applications for the
Spring Valley hydrographic basin.
SNWA can pump 4,877 ha-m (40,000
ac-ft) annually from the basin, with the
potential for an additional 2,438 ha-m
(20,000 ac-ft) based on results of 10
years of monitoring that will be
conducted for the initial pumping
allocation (NSE 2007, p. 56). The
Nevada State Engineer hearings on
SNWA water rights applications in
Snake Valley are projected for fall 2009.
In addition to the water awarded to
SNWA in Spring Valley, filings for 6251
ha-m (50,680 ac-ft) in Snake Valley are
pending.
New, large-volume filings in the State
of Utah include: Millville Irrigation
Co.—15172 ha-m (123,000 ac-ft) in Wah
Wah Valley; the Confederate Tribes of
the Goshute Reservation—6168 ha-m
(50,000 ac-ft) in Deep Creek Valley;
Central Iron County Water Conservancy
District—4564 ha-m (37,000 ac-ft) in
Hamlin, Pine, and Wah Wah Valleys;
private parties in Snake Valley—1294
ha-m (10,490 ac-ft); and the State of
Utah School and Institutional Trust
Lands—1105 ha-m (8960 ac-ft) in Snake
Valley (UGS 2008, entire). We did not
receive information detailing future
plans for development on the filings of
these Utah water rights.
The SNWA GWD Project is
anticipated to be completed and may
begin pumping in January 2014 (SNWA
2007, pp. 4–11). Prior to its completion,
baseline data collection and research on
biologic and hydrologic impacts will be
completed and an intensive monitoring
program will be put in place to monitor
and mitigate for Project effects. At the
present time, SNWA anticipates that
ultimately between 110 and 200
groundwater production wells may be
required for the GWD Project. However,
the specific locations of these wells are
dependent upon future rulings from the
Nevada State Engineer, exploratory
drilling results, agency agreements, and
results of actual groundwater pumping.
SNWA anticipates that it may take up to
20 years or more to site and install all
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of the groundwater production wells for
the project (SNWA 2007, p. 2–1).
A great deal of uncertainty exists
regarding the long-term effects of the
groundwater pumping for aquifers and
surface waters in the Great Basin.
However, well locations will generally
be sited in valley bottoms and be
withdrawing water from deep carbonate
and alluvial aquifers. BCT populations
are generally located in headwater
streams in the West Desert GMU, and it
is anticipated that direct effects to BCT
populations and their habitat will be
minimal or nonexistent. Additionally,
SNWA entered into a stipulation with
the Department of the Interior regarding
SNWA’s GWD Project water
withdrawals in the Spring Valley
hydrographic basin. The goals of this
stipulation include avoidance of any
effects to water-dependent ecosystems
within the boundaries of Great Basin
National Park and avoidance of
unreasonable adverse impacts to waterdependent ecosystems in the remainder
of the project area. This will be
accomplished through hydrologic and
biologic monitoring, management, and
mitigation plans designed to identify,
avoid, and mitigate effects of
groundwater withdrawal on dependent
ecosystems (SNWA 2008, p. 15).
It has been hypothesized that water
development in two areas of the GWD
Project, the Spring Valley and Snake
Valley Basins, could have indirect
effects to BCT habitats in the West
Desert GMU. Groundwater pumping
could result in the lowering of valley
water tables and spring discharge rates
and result in drying and desiccation of
wetland and riparian phreatophytic
(deep rooted) vegetation. This could
likely result in an increase in fire
frequency in Great Basin valley floors
that are adjacent to drainages that have
BCT populations in headwater streams.
Riparian vegetation in drainages of the
Snake and Deep Creek ranges where
BCT occur could become more
susceptible to these fires. However,
there is a great deal of uncertainty as to
whether this scenario will occur or if it
will have impacts to BCT as no
information exists regarding what the
actual effects of pumping would be to
valley vegetation or fire frequency. At
this time, we know of no information
that indicates to us that groundwater
pumping in the West Desert GMU is
significantly affecting BCT now or into
the foreseeable future.
Summary of Factor E
Despite the potential for increased
risk to BCT populations resulting from
future climate change, we found no
scientific and commercial information
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leading us to conclude that climate
change is currently a significant threat
to BCT conservation populations, or
will become so within the foreseeable
future.
We assessed the potential risks to BCT
conservation populations associated
with fragmentation and isolation of
small BCT conservation populations,
including stochastic, catastrophic,
natural events, and find that they do not
now, nor will in the foreseeable future,
significantly threaten the status of BCT
to the extent that listing under the Act
as a threatened or endangered species is
warranted.
We assessed the potential threats
posed by nonnative species, including
historical stocking, competition, and
introgressive hybridization with
rainbow trout or other cutthroat
subspecies. Nonnative fish species exist
in 63 percent of occupied BCT habitat.
However, 61 percent of BCT
populations are isolated from nonnative
fish by natural or constructed barriers,
and stocking of nonnative fish no longer
occurs in BCT waters. These factors,
combined with the current distribution
of conservation populations, indicate
that nonnatives do not currently affect
the status of BCT to the extent that
listing under the Act as a threatened or
endangered species is warranted. In
addition, management practices focused
on removing and preventing
introduction of nonnative fish within
BCT habitat, provide reasonable
assurance that this potential threat
factor will not increase within the
foreseeable future.
Foreseeable Future
In the context of the Act, 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 term ‘‘endangered species’’ means
any species that is in danger of
extinction throughout all or a significant
portion of its range. The Act does not
define the term foreseeable future;
however, we consider it to be affected
by the biological and demographic
characteristics of the species, as well as
our ability to predict or extrapolate the
effects of threats facing the species in
the future. Quantification of the time
period corresponding to the foreseeable
future is challenging because it
necessitates making predictions about
inherently dynamic political, legal, and
social mechanisms that influence the
degree and immediacy of potential
threats to the species.
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For the purpose of this finding, the
‘‘foreseeable future’’ is the period of
time over which events or effects
reasonably can or should be anticipated,
or trends reasonably extrapolated, such
that reliable predictions can be made
concerning the status of the species in
the future. Although we have found
some threats to BCT are ongoing at low
levels and that various localized areas
may be affected by specific problem
activities, as discussed in the Summary
of Factors section, we did not find any
information to suggest that threats will
rise to levels that would significantly
threaten BCT rangewide to the extent
that the species would warrant listing
under the Act.
Although we did not find any
information to allow us to reliably
predict that threats would increase
significantly in the future, predicting
and managing for the effects of potential
future threats will be facilitated by the
BCT conservation plans that are in place
at the State and rangewide level (see
Conservation Actions section under
Factor D). Monitoring of BCT
population numbers and habitat
conditions is included in the State and
rangewide conservation plans and any
significant decreases in BCT
populations or habitat conditions
should be identified and effectively
mitigated by using the methods
developed in these conservation plans.
State and Federal agency participation
in BCT conservation plans is voluntary;
however, State plans are typically in
place indefinitely, or have a term of
agreement for 5–10 years with renewal
provisions for a similar time period. The
rangewide BCT conservation agreement
was renewed in 2008 for 10 years with
the commitment that it would be
extended for an additional 10 years
upon expiration. In addition, the States
within the range of the BCT have an
established record of managing for the
species (see Factor D). We find that the
BCT conservation plans will be in place
and operating for at least 20 years. We
consider the status of the BCT to be
reasonably predictable with established
management practices in place because
many of the threats to the species are
effectively mitigated by these practices;
outside the timeframe of the
conservation plans, we are unable to
make reliable predictions regarding the
threats to the species and the effect of
those threats on the status of the
species. Therefore, the foreseeable
future for BCT is 20 years with respect
to most threats.
Our ability to predict the effects of
future threats is limited to our
knowledge of the timeframe of the
threats potentially facing the BCT, and
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the conservation activities taking place
to address them. We assessed activities
that could potentially affect BCT
populations under the Summary of
Factors section. Livestock grazing was a
concern in the early 1900’s, but recent
management practices appear to have
reduced effects to watersheds, and these
practices are expected to continue for at
least 20 years. Road construction or
maintenance, timber harvest, and water
diversions and depletions are expected
to be managed consistently within at
least the next 20 years, and are not
expected to result in a downward trend
in BCT population status. The
foreseeable future for oil and gas
development is possibly shorter than for
other threats (i.e., less than 20 years),
because this threat is not specifically
mitigated by conservation actions
identified in the State conservation
plans; however, oil and gas
developments are mostly outside the
historic range of the BCT, and are not
creating a downward trend in
population status. Recreational angling
is currently regulated, and no
downward trend in population status
exists due to this activity. Disease in
BCT is being mitigated through
conservation actions that are expected
to continue for at least the next 20 years.
Factors related to the presence of
nonnative fish species, such as
predation, competition, and genetic
introgression, are being mitigated
through conservation actions that are
expected to continue for at least the next
20 years.
Climate change projections are
considered fairly robust for the current
century on a continental scale, but, as
discussed above, we cannot yet make
reliable predictions as to the magnitude
or timing of likely temperature increases
within the range of the BCT. Therefore,
for the purposes of analyzing the threat
of climate change to the BCT, the future
is only foreseeable to the extent of our
determination that some additional
temperature increase is likely. We
cannot determine that the BCT will
become endangered due to an
unquantifiable amount of temperature
increase, particularly given the BCT’s
apparent adaptability to a relatively
broad spectrum of habitat conditions,
although we recognize that it is possible
that climate change will eventually have
more significant impacts.
We have determined that the
immediacy and magnitude of the abovementioned threats will not significantly
degrade the 80 percent of BCT habitat
that is currently in fair to excellent
condition within the next 20 years, in
part due to regulatory mechanisms and
management practices (no nonnative
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stocking, combined with nonnative
removal programs) that have been
implemented and shown to be effective
by State and Federal management
agencies, and that we have reasonable
assurance will continue for at least the
next 20 years.
Significant Portion of the Range
As required by the Act, we considered
the five potential threat factors to assess
whether the BCT is threatened or
endangered throughout all or a
significant portion of its range. When
considering the listing status of a
species, the first step in the analysis is
to determine whether the species is in
danger of extinction throughout all of its
range. If this is the case, then we list the
species in its entirety. For instance, if
the threats to a species are directly
acting on only a portion of its range, but
they are at such a large scale that they
place the entire species in danger of
extinction, we would list the entire
species.
Based on the best available scientific
and commercial information available
addressing BCT distribution and
potential threats, especially the
rangewide status report for BCT (May
and Albeke 2005, entire), we find that
the BCT is not likely to become
endangered in the foreseeable future
throughout all of its range.
On March 16, 2007, a formal opinion
was issued by the Solicitor of the
Department of the Interior, ‘‘The
Meaning of ‘In Danger of Extinction
Throughout All or a Significant Portion
of Its Range’ ’’ (DOI 2007). A portion of
a species’ range is significant if it is part
of the current range of the species and
is important to the conservation of the
species because it contributes
meaningfully to the representation,
resiliency, or redundancy of the species.
The contribution must be at a level such
that its loss would result in a decrease
in the ability to conserve the species.
We evaluated the BCT throughout its
current range to determine if any
portion is likely to become threatened or
endangered within the foreseeable
future, and if so, whether that portion is
important to the conservation of the
species because it contributes
meaningfully to the resiliency,
representation, or redundancy of the
species.
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
portions that warrant further
consideration, we determine whether
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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.
If we identify portions of the range
that warrant further consideration, we
determine whether the species is
threatened or endangered in any
significant portion of its range.
Depending on the biology of the species,
its range, and the threats it faces, it may
be more efficient to address the
significance question first, or the status
question first. If we determine that a
portion of the range is not significant,
we need not determine whether the
species is threatened or endangered
there; similarly, if we determine that the
species is not threatened or endangered
in a portion of its range, we need not
conduct significance analysis.
The concepts of ‘‘resiliency,’’
redundancy,’’ and ‘‘representation’’ are
indicators of the conservation value of
portions of the range. Resiliency of a
species allows the species to recover
from periodic disturbance. A species
will likely be more resilient if large
populations exist in high-quality habitat
that is distributed throughout the range
of the species in such a way as to
capture the environmental variability
found within the range of the species. It
is likely that the larger size of a
population will help contribute to the
viability of the species overall.
Therefore, a portion of the range of a
species may make a meaningful
contribution to the resiliency of the
species if the area is relatively large and
contains particularly high-quality
habitat or if its location or
characteristics make it less susceptible
to certain threats than other portions of
the range.
Redundancy of populations may be
needed to provide a margin of safety for
the species to withstand catastrophic
events. This does not mean that any
portion that provides redundancy is a
significant portion of the range of a
species. The idea is to conserve enough
areas of the range such that random
perturbations in the system act on only
a few populations. Therefore, each area
must be examined based on whether
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that area provides an increment of
redundancy that is important to the
conservation of the species.
Adequate representation insures that
the species’ adaptive capabilities are
conserved. Specifically, the portion
should be evaluated to see how it
contributes to the genetic diversity of
the species. The loss of genetically
based diversity may substantially
reduce the ability of the species to
respond and adapt to future
environmental changes. A peripheral
population may contribute meaningfully
to representation if there is evidence
that it provides genetic diversity due to
its location on the margin of the species’
habitat requirements.
We assessed threats at the watershedbased GMU level, because standardized
fish monitoring methods and BCT
management methods are watershed
based. The four GMUs are
geographically and hydrologically
distinct; they also delineate BCT
populations in logical biogeographical
and taxonomic subgroups. Based on the
best available scientific and commercial
information regarding the abundance of
BCT, and our assessment of threats to
the species, throughout its current
range, we find that no individual GMU
is likely to become threatened or
endangered in the foreseeable future
because threats are evenly distributed
throughout the range of the species.
Further subdividing of BCT
populations or habitat into smaller
portions than GMUs would require
unscientific methodology. In addition,
smaller subdivisions of populations
would not, individually, be significant
to the subspecies. We find that areas
smaller than the GMU would not
meaningfully contribute to the
resilience, redundancy, or
representation of the BCT. Losses of
habitat or species from areas smaller
than the GMU level would not threaten
the entire GMU, and a sufficient number
of GMUs exist to ensure species
redundancy and resiliency. No
significant ecological differences exist at
levels smaller than the GMUs to affect
representation of the subspecies.
Threats are similar in all four GMUs,
and no individual GMU has threats of
a magnitude that the subspecies is
threatened or endangered within it.
Therefore, we have determined that no
significant portion of the BCT range is
in danger of extinction or likely to
become so within the foreseeable future.
Distinct Vertebrate Population Segment
(DPS)
Pursuant to section 4(a)(1) of the Act,
we must determine whether any species
is an endangered species or a threatened
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species because of any of the threat
factors identified therein. Section 3(15)
of the Act defines ‘‘species’’ to include
‘‘any species or subspecies of fish and
wildlife or plants, and any distinct
vertebrate population segment of fish or
wildlife that interbreeds when mature’’
(16 U.S.C. 1532 (16)). To interpret and
implement the distinct vertebrate
population portion of the definition of
a species under the Act and
congressional guidance, the Service and
the National Marine Fisheries Service
(now the National Oceanic and
Atmospheric Administration—
Fisheries) published, on February 7,
1996, an interagency Policy Regarding
the Recognition of Distinct Vertebrate
Population Segments under the Act
(DPS Policy; 61 FR 4722). The policy
allows for more refined application of
the Act that better reflects the
conservation needs of the taxon being
considered, and avoids the inclusion of
entities that may not warrant protection
under the Act.
Under our DPS policy, three elements
are considered in a decision regarding
the status of a possible DPS as
endangered or threatened under the Act.
These are applied similarly for
additions to the List of Endangered and
Threatened Wildlife and Plants,
reclassification, and removal from the
List. They are: (1) Discreteness of the
population segment in relation to the
remainder of the taxon; (2) the
significance of the population segment
to the taxon to which it belongs; and (3)
the population segment’s conservation
status in relation to the Act’s standards
for listing (i.e., whether the population
segment is, when treated as if it were a
species, endangered or threatened).
Discreteness refers to the isolation of a
population from other members of the
species and we evaluate this based on
specific criteria. If a population segment
is considered discrete, we must consider
whether the discrete segment is
‘‘significant’’ to the taxon to which it
belongs by using the best available
scientific information. If we determine
that a population segment is discrete
and significant, we then evaluate it for
endangered or threatened status based
on the Act’s standards.
We assessed threats at the watershedbased GMU level, because standardized
fish monitoring methods and BCT
management methods are watershed
based. The four GMUs are
geographically and hydrologically
distinct; they also delineate BCT
populations in logical biogeographical
and taxonomic subgroups. In addition,
each GMU is significant to the
continued existence of the species.
However, based on the best available
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scientific and commercial information
regarding the abundance of BCT, and
our assessment of threats to the species,
throughout its current range, we find
that no individual GMU is likely to
become threatened or endangered in the
foreseeable future because threats are
evenly distributed throughout the range
of the species.
The four GMUs meet the first two
criteria in the DPS policy, but the
conservation status of each is stable.
Further subdividing of BCT populations
or habitat into smaller portions than
GMUs would require unscientific
methodology. In addition, while it is
possible that smaller units would meet
the discreteness criteria in the DPS
policy, it is unlikely that any smaller
area would be significant to the
subspecies.
Finding
This status review includes
substantial information that was not
available at the time of the 2001 status
review and 12-month finding (66 FR
51362), in particular, the information
obtained from May and Albeke (2005).
We requested a peer review of May and
Albeke (2005); peer reviews were
conducted by five recognized cutthroat
trout experts who found that the
document provided sound scientific
data on the rangewide status of BCT.
Populations of BCT have been greatly
reduced over the last 200 years, with
much loss occurring in the late 19th and
early 20th century (Behnke 1992, pp.
132–138). However, recent surveys have
shown that the numbers of BCT
populations have increased in the last 3
decades and the subspecies remains
widely distributed throughout a large
geographic area. We attribute the
historic decline in the distribution of
BCT to the introduction of nonnative
sport fish into BCT habitat that began in
the late 1800s. The wide distribution of
rainbow trout and nonnative cutthroat
trout caused problems through
competition, hybridization, and
predation. In some places, introduced
fish expanded and colonized new
habitat, and formed naturally
reproducing populations that occupy
the former, and in some cases current,
range of BCT.
We found no evidence of continuing
declines in the overall distribution or
abundance of BCT during the last
several decades. A substantial increase
in the number of known populations
has been documented (May and Albeke
2005, pp. 63–64), and habitat quality is
good to excellent in over half (52
percent) of BCT habitat, and fair to
excellent in 80 percent of BCT habitat.
Management agencies have focused on
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the protection and restoration of
conservation populations of BCT in all
currently occupied watersheds.
Additional focus is on habitat
restoration activities and fisheries
management actions designed to benefit
BCT. Some recognized threats to BCT,
such as excessive harvest by anglers and
stocking of nonnative fishes, are now
regulated or discontinued so that they
no longer threaten the continued
existence of BCT. Conservation actions
have resulted in improved population
levels in some areas (Ottenbacher 2008,
entire).
At least 153 BCT conservation
populations collectively occupy about
3,316 km (2,061 mi) of stream habitat in
22 watersheds (HUCs) in Utah, Idaho,
Nevada, and Wyoming. These
populations qualify as conservation
populations of BCT under standards
developed by the States that are
consistent with our assessment of best
available science. Conservation
populations are distributed throughout
the four GMUs within the historic range
of the BCT. Of the 153 conservation
populations identified by May and
Albeke (2005, p. 31), about 71 (46
percent) are core populations comprised
of nonintrogressed BCT (greater than 99
percent genetic purity).
Hybridization, mostly with nonnative
rainbow trout and nonnative subspecies
of cutthroat trout that have established
self-sustaining populations in many
areas in the range of BCT, has
historically been an issue of
management concern. However, current
State management has greatly reduced
opportunities for further genetic
introgression. States continue to
monitor introgression in BCT
throughout its range. We find that the
limited presence of genetic material
from other fish species or subspecies
(typically less than 10 percent) is not a
threat to BCT conservation populations.
Populations or individual fish with a
low level of introgression are
morphologically, ecologically, and
behaviorally indistinguishable from
nonintrogressed (i.e., pure) BCT.
Slightly introgressed BCT populations,
with low amounts of genetic
introgression detectable only by
molecular genetic methods (i.e.,
conservation populations), are an
important component of BCT
conservation. Genetically pure
populations (71 core populations) are
distributed throughout the current range
of BCT. State and Federal agencies are
implementing strategies and actions to
protect BCT populations from invasion
of nonnative species or subspecies that
may interbreed with BCT.
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Brook trout, brown trout, and rainbow
trout compete with BCT where they are
sympatric. Managers are monitoring
competition from nonnative fish in BCT
waters, and implementing ongoing
management strategies and actions to
curtail it. However, 1,365 km (848 mi)
of habitat occupied by BCT conservation
populations are free of nonnative trout.
The BCT persists as a widely
distributed subspecies; 153 conservation
populations exist throughout the
historic range, and a metapopulation
structure exists in each GMU.
Nonintrogressed BCT core populations
exist in habitats secure from nonnative
trout and thus are protected from
potential hybridization throughout the
subspecies’ historic range. Although
distribution of BCT has been reduced
from historic levels (the subspecies now
occupies about 35 percent of historic
habitat), the 2005 rangewide status
report on BCT documented the
continued existence of conservation
populations throughout its current
range, and that 80 percent of occupied
habitat is in fair to excellent condition.
We have thoroughly assessed the
current status of BCT, the mitigation of
existing threats, and the existence of
laws and regulations that minimize
adverse effects of land management and
other activities on BCT. We find that the
magnitude and imminence of threats do
not indicate that the subspecies is in
danger of extinction, or likely to become
endangered, throughout all or any
significant portion of its range, within
the foreseeable future. Therefore, we
find that listing the BCT as a threatened
or an endangered species under the Act
is not warranted at this time.
References Cited
A complete list of all references cited
herein is available upon request from
the Utah Ecological Services Field
Office (see ADDRESSES section).
Author
The primary author of this document
is the staff of the U.S. Fish and Wildlife
Service, Utah Ecological Services Field
Office (see ADDRESSES section).
Authority: The authority for this action is
the Endangered Species Act of 1973, as
amended (16 U.S.C. 1531 et seq.).
Dated: August 29, 2008.
Kenneth Stansell,
Acting Director, U.S. Fish and Wildlife
Service.
[FR Doc. E8–20674 Filed 9–8–08; 8:45 am]
BILLING CODE 4310–55–P
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[FR Doc No: E8-20674]
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DEPARTMENT OF THE INTERIOR
Fish and Wildlife Service
50 CFR Part 17
[FWS-R6-ES-2008-0023; 1111 FY07 MO-B2]
Endangered and Threatened Wildlife and Plants; 12-Month Finding
on a Petition To List the Bonneville Cutthroat Trout as Threatened or
Endangered
AGENCY: Fish and Wildlife Service, Interior.
ACTION: Notice of a 12-month petition finding.
-----------------------------------------------------------------------
SUMMARY: We, the U.S. Fish and Wildlife Service (Service), announce our
12-month finding on a petition to list the Bonneville cutthroat trout
(Oncorhynchus clarkii utah) as a threatened subspecies throughout its
range in the United States, pursuant to the Endangered Species Act of
1973, as amended (Act). After a thorough review of all available
scientific and commercial information, we find that listing the
Bonneville cutthroat trout as either threatened or endangered is not
warranted at this time. We ask the public to continue to submit to us
any new information that becomes available concerning the status of or
threats to the subspecies. This information will help us to monitor and
encourage the conservation of the subspecies.
DATES: The finding in this document was made on September 9, 2008.
ADDRESSES: This finding is available on the Internet at https://
www.regulations.gov. Supporting documentation we used in preparing this
finding is available for public inspection, by appointment, during
normal business hours at the U.S. Fish and Wildlife Service, Utah
Ecological Services Office, 2369 West Orton Circle, Suite 50, West
Valley City, Utah 84119; telephone (801) 975-3330. Please submit any
new information, materials, comments, or questions concerning this
finding to the above address or via electronic mail (e-mail) at paul_
abate@fws.gov.
FOR FURTHER INFORMATION CONTACT: Larry Crist, Field Supervisor, U.S.
Fish and Wildlife Service, Utah Ecological Services Office (see
ADDRESSES section). 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 Endangered Species Act of 1973, as
amended (Act) (16 U.S.C. 1531 et seq.), requires that, for any petition
to revise the List of Endangered and Threatened Species that contains
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 the 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 List of Endangered and Threatened Species.
Section 4(b)(3)(C) of the Act requires that a petition for which the
requested action is found to be warranted but precluded be treated as
though resubmitted on the date of such finding, that is, requiring a
subsequent finding to be made within 12 months. Such 12-month findings
must be published in the Federal Register.
Previous Federal Actions
On February 26, 1998, we received a petition, dated February 5,
1998, from the Biodiversity Legal Foundation requesting that the
Service list the Bonneville cutthroat trout (Oncorhynchus clarkii utah)
(BCT) as threatened in U.S. river and lake ecosystems where it
continues to exist, and to designate its occupied habitat as critical
habitat within a reasonable period of time following the listing. On
December 8, 1998, we published a 90-day petition finding for the BCT in
the Federal Register (63 FR 67640). We found that the petition
presented substantial information indicating that the subspecies may be
warranted for listing under the Act, and initiated a review of the
subspecies' status within its historic range.
In the 1998 90-day finding, we solicited additional data, comments,
and suggestions from the public, other governmental agencies, the
scientific community, industry, and other interested parties concerning
the status of the BCT throughout its range. The comment period for
submission of additional information ended on January 7, 1999, but was
reopened (64 FR 2167) during January 13 through February 12, 1999. We
published a 12-month finding in the Federal Register on October 9, 2001
(66 FR 51362), and documented that the BCT was not warranted for
listing under the Act because it was neither endangered nor likely to
become endangered within the foreseeable future throughout all or a
significant portion of its range.
On February 17, 2005, we were sued by the Center for Biological
Diversity, and others, on the merits of the 12-month finding. On March
7, 2007, the District Court of Colorado dismissed the lawsuit after
determining that Plaintiffs failed to demonstrate the not warranted
finding was arbitrary, capricious, or contrary to law. The Plaintiffs
appealed to the 10th Circuit Court of Appeals on May 4, 2007.
On March 16, 2007, in the interim between the lawsuit dismissal and
appeal, the Solicitor of the Department of the Interior issued a formal
opinion regarding the legal interpretation of the term ``significant
portion of the range'' of a species (DOI 2007). The opinion provides
guidance on analysis intended to determine whether a species is in
danger of extinction throughout a significant portion of its range when
it is not in danger of extinction throughout its entire current range.
Because this opinion was pertinent to the BCT decision, we withdrew the
2001 12-month finding for BCT (USFWS 2007, entire), and initiated a new
status review to include significant portion of the range analysis. We
published a notice in the Federal Register (73 FR 7236) announcing the
opening of a comment period from February 7 through April 7, 2008. The
notice specified that the new status review would include consideration
and analysis of all information previously submitted, and any new
information provided regarding the status of the BCT.
Species Biology
The BCT is native to the Bonneville basin, and is 1 of 14
subspecies of cutthroat trout recognized by Behnke (1992, pp. 3-21,
132-138) that are native to interior regions of western North America.
BCT generally have large, evenly distributed spots, but a high degree
of intra-basin variation exists. BCT tend to develop large, pronounced
spots that are evenly distributed on the sides of the body rather than
concentrated posteriorly as in the Yellowstone cutthroat trout
(Oncorhynchus clarkii bouveri)
[[Page 52236]]
subspecies. Coloration in BCT is generally dull compared to other
cutthroat subspecies; however, coloration can vary depending on
environmental conditions and local genetic composition (Behnke 1992,
pp. 132-138).
Vertebrae typically number 62-63, slightly higher than in other
subspecies. Scales in lateral series average 150-170. BCT average
between 16-21 gill rakers, with a mean of 18-19, except the Snake
Valley type, which have 18-24 (mean, 20-22). Another important
characteristic of all cutthroat subspecies is the presence of
basibranchial teeth, which are absent in rainbow trout (Behnke 1992, p.
132). Numbers of basibranchial teeth provide information about
subspecies derivation and relatedness. The Snake Valley type have
profuse basibranchial teeth, averaging 20-28, while most other BCT
average 5-10 (Behnke 1992, p. 132).
Life strategies exhibited by BCT include stream resident (occupy
home ranges entirely within relatively short reaches of streams),
fluvial (migrate as adults from larger streams or rivers to smaller
streams to reproduce), adfluvial (migrate, sometimes many kilometers,
as mature adults from lakes to inlet or outlet streams to spawn), and
lacustrine (lake) forms. The life strategy that a particular BCT
population exhibits likely depends on a combination of environmental
conditions and genetic plasticity of inherited traits. Very little
information is available to suggest the extent of plasticity and what
environmental characteristics may cue a successful shift in life
strategy. Most information is based on the success or failure of
transplants of various life forms among different aquatic ecosystems.
Furthermore, evidence suggests that BCT populations within a single
stream can comprise multiple life history strategies (resident,
fluvial, adfluvial), and that individuals may use mainstem rivers to
move between and among drainages where they are not fragmented by water
diversions or barriers (Kershner et al. 1997, entire).
May et al. (1978, p. 19) found that male BCT sexually matured at
age 2 while females matured at 3 years of age. However, Bear Lake BCT
were reported to mature much later, with adults normally beginning to
mature at 5 years of age but not spawning until age 10 (Neilson and
Lentsch 1988, p. 131). Both the age at maturity and the annual timing
of spawning vary geographically with elevation, temperature, and life
history strategy (Behnke 1992, p. 136; Kershner 1995, pp. 28-30). Lake
resident trout may begin spawning at 2 years and usually continue
throughout their lives, while adfluvial individuals may not spawn for
several years (Kershner 1995, pp. 28-30). Annual spawning of BCT
usually occurs during the spring and early summer at higher elevations
at temperatures ranging from 4-10 [deg]C (May et al. 1978, p. 19). May
et al. (1978, p. 19) reported BCT spawning in Birch Creek, Utah,
beginning in May and continuing into June. BCT in Bear Lake began
spawning in late April and completed spawning in June (Nielson and
Lentsch 1988, p. 131). The wild broodstock at Manning Meadow Reservoir
(9,500 feet elevation) spawn from late June to early July (Hepworth and
Ottenbacher 1997, p. 1). In Lake Alice, Wyoming, fish were predicted to
spawn from late May until mid-June (Binns 1981, p. 47).
Fecundity of cutthroat is typically 1,200-3,200 eggs per kilogram
(kg) (2.2 pounds (lbs)) of body weight (Behnke 1992, p. 33). In Birch
Creek, a 147 millimeters (mm) (5.8 inches (in)) BCT female produced 99
eggs, a 158 mm (5.8 in) female produced 60 eggs and a 176 mm (6.9 in)
female produced 176 eggs (May et al. 1978, p. 19). Whereas in Raymond
Creek, Wyoming, 3 females ranging from 124 to 246 mm (4.9 to 9.7 in)
averaged 165 eggs (Binns 1981, p. 48). Evidence suggests fecundity of
lake-dwelling BCT is greater. Fecundity of females in Lake Alice
averaged 474 eggs/female (Binns 1981, p. 48), while females in Manning
Meadow, Utah, averaged 994 eggs/female (D. Hepworth, Utah Division of
Wildlife Resources, unpubl. data). Incubation times for wild BCT have
not been verified, but Platts (1957, p. 10) suggested eggs hatch and
fry begin to emerge approximately 45 days after spawning, depending on
temperature.
Larvae typically emerge in mid-to-late summer, depending on
spawning times. Once emerged, larvae or fry, as they are commonly
called, are poor swimmers and typically migrate to stream margins.
Adfluvial BCT spend 1 or 2 years in streams before migrating to the
Lake (Nielson and Lentsch 1988, p. 131).
Growth of resident BCT is highly dependent on stream productivity.
In general, growth of trout tends to be slower in high-elevation
headwater drainages than in lacustrine environments, but this likely
depends on temperatures and food base. In Birch Creek, Utah, age 1 fish
averaged 84 mm (3.3 in), age 2 fish averaged 119 mm (4.7 in), age 3
fish averaged 158 mm (6.2 in), and age 4 fish averaged 197 mm (7.8 in)
in length (May et al. 1978, p. 17). Growth in two Wyoming streams was
faster, and age 4 fish averaged 282 to 320 mm (11.1 to 12.6 in) in
length (Binns 1981, p. 44). In contrast, BCT in Bear Lake grow to an
average size of 560 mm (22.0 in) and 2 kg (4.4 lbs) (Nielson and
Lentsch 1988, p. 131). Historic accounts of BCT in Utah Lake suggest
fish may have reached a meter in length (Notes from Yarrow and Henshaw
in 1872 as described by Tanner 1936). Platts (1957, p. 10) reported
that some BCT taken from Utah Lake a century ago attained weights of
over 11.3 kg (25 lbs).
Little is known about feeding habits of BCT. In general, BCT trout
are insectivorous, especially in stream habitats. Both terrestrial and
aquatic insects appear to be important to their diet (May et al. 1978,
pp. 7-10; Binns 1981, p. 48). In Birch Creek, May et al. (1978, pp. 9-
10) reported BCT diets were diverse in summer, while in the fall in
Trout Creek, Utah, their diet consisted primarily of terrestrial
insects. Dipterans and debris were the dominant food items for immature
trout, while terrestrial insects were the dominant prey for mature
individuals. BCT may display more plasticity in feeding habits
depending on the system or specific population characteristics. Little
information has been collected on BCT to understand the extent of
feeding shifts of BCT. Platts (1957, p. 4) suggested that cutthroat do
not need to feed on fish to attain large sizes but will do so where
insects are not abundant.
Interactions With Nonnative Fish
BCT may or may not persist when nonnative trout are stocked into
BCT waters. The actual mechanism that dictates the survivorship of BCT
in the presence of nonnatives is unknown, but the recent discovery that
numerous BCT populations have persisted for decades in the presence of
rainbow trout (Oncorhynchus mykiss), Yellowstone cutthroat trout, and
other nonnatives suggests BCT is not always displaced by nonnatives as
previously thought. However, BCT can hybridize with rainbow trout and
Yellowstone cutthroats in some situations and be displaced by the
superior competitor, brook trout (Salvelinus fontinalis). The degree of
hybridization appears to vary with the persistence of the stocked fish
and also with habitat conditions as does the level of competition with
brook trout.
Benhke (1992, p. 107) reported that BCT native to the Bear River
drainage adapted to the harsh and fluctuating environments of desert
basin streams, remaining the dominant trout today in many streams where
nonnative trout were introduced. This seems to be a fairly unique trait
of BCT compared to other cutthroat subspecies. There is still no
specific rationale as to why BCT would persist better than other desert
[[Page 52237]]
cutthroat subspecies, yet something in its unique genetic composition
seems to allow BCT to persist where other cutthroat subspecies have
been found to be displaced.
For example, Bear Lake BCT, probably due to the unique
environmental conditions in which they developed, have resisted
hybridization with and replacement by nonnative trout. Yellowstone
cutthroat trout, Yellowstone cutthroat rainbow trout hybrids, and
rainbow trout were consistently stocked into Bear Lake for decades.
Benhke (1992, p.137) examined specimens from Bear Lake and compared
these to museum specimens from the lake and with cutthroat trout from
the Bear River drainage and found no evidence of hybridization among
their taxonomic characters. Nielson and Lentsch (1988, p.130) similarly
reported that, after examining the DNA of 52 Bear Lake specimens, no
rainbow trout alleles were observed in any fish.
Since the early 1990's, many additional remnant BCT populations
have been found in streams that had been stocked with rainbow trout or
Yellowstone cutthroat trout (Utah Division of Wildlife Resources,
unpublished data). These BCT populations were assumed to be lost
through hybridization until recent surveys found BCT present. Results
of these surveys suggest BCT have retained much of their natural
genetic integrity despite intensive nonnative stocking efforts.
Introduced brook trout have been stocked, legally and illegally,
into some BCT waters. BCT do not hybridize with brook trout, but brook
trout are thought to acquire resources better and reproduce and recruit
more efficiently than BCT. The specific mechanism of how brook trout
displace BCT is unknown, but greater fecundity, earlier maturity, and
tolerance of higher densities gives brook trout an advantage over the
native BCT (Griffith 1988, p. 105; Fausch 1989, pp. 307-312). The
extent of threat to BCT from brook trout varies depending on
environmental conditions of the stream. Although not considered the
greatest threat to the persistence of BCT, competition from introduced
brook trout can and has displaced native BCT populations.
Habitat Requirements
Trout, regardless of their evolutionary history, require 4 types of
habitat during various stages of their life history: spawning habitat,
nursery or rearing habitat, adult habitat, and overwintering habitat.
Spawning gravels are required for spawning success and can be a
limiting factor in high-gradient streams where the current carries off
suitable spawning gravel (Behnke 1992, p. 25). Conversely, an even
greater concern may be accumulation of fine sediments into interstitial
spaces of spawning gravels, which prevents egg incubation and reduces
larval survival. Such fines can become dominant in the sediments when
poor land-use practices alter flow regimes, remove riparian vegetation,
and/or degrade overall watershed conditions. These human-induced
activities can aggravate already fragile soils and geology in
vulnerable desert climates.
Little information is available on specific habitat requirements
for BCT; however, there is a wealth of information on salmonid habitat
conditions in general which appear to generally represent those of BCT
(Pennak and Van Gerpen 1947, entire; Binns and Eiserman 1979, entire;
Scarnecchia and Bergersen 1987, entire). For example, well-oxygenated
water, cooler temperatures in general and a complexity of instream
habitat structure, such as large woody debris and overhanging banks,
are considered good trout habitat conditions. For various species,
subspecies, and local forms, adaptations and tolerance of these
conditions varies. BCT have also been found to survive and be fairly
robust in what is considered marginal salmonid habitat conditions
(e.g., turbid water, fine sediments, warmer temperatures, poor
structural habitat). This may be because BCT have evolved in a desert
environment where climate can cause fluctuations in water and sediment
regimes and environmental condition (Behnke 1992, p. 107).
It was previously thought that with the exception of three
lacustrine systems, Bear Lake (Utah and Idaho), Utah Lake, and Alice
Lake (Wyoming), BCT were historically found in cool headwater streams
throughout the Bonneville basin. However, more recent research and
status and genetic surveys reveal BCT populations are found at high,
moderate, and low elevations (within the range of elevations in the
Bonneville Basin) in small headwater streams, such as those of the
north slope of the western Uintas, to larger mainstem rivers, such as
the Thomas Fork of the Bear River (UDWR, unpublished data).
Historic Habitat
BCT likely historically occupied all suitable habitats within the
Pleistocene Lake Bonneville basin, which included portions of Idaho,
Nevada, Utah, and Wyoming. The desiccation of ancient Lake Bonneville
about 8,000 years ago likely fragmented the BCT into remaining streams
and lakes throughout the basin, resulting in several slightly
differentiated groups of BCT, including: (1) The Bear River basin; (2)
the Bonneville basin proper, including the Wasatch Mountain and Sevier
River drainages; and (3) the Snake Valley, an arm of ancient Lake
Bonneville that was isolated during an earlier desiccation event
(Behnke 1992, pp. 132-138). There is general consensus among the
scientific community, including the Service, that all these groups
represent the BCT subspecies (Shiozawa 2008, p. 1). For the purposes of
this finding, all three groups are considered BCT.
The BCT Conservation Team, which includes biologists from Wyoming
Game and Fish Department (WGFD), Utah Division of Wildlife Resources
(UDWR), Nevada Division of Wildlife (NDOW), Idaho Department of Fish
and Game (IDFG), Bureau of Land Management (BLM), U.S. Forest Service
(USFS), the National Park Service (NPS), and the Service, completed a
status report (May and Albeke 2005) that describes the rangewide status
of BCT in the United States. The rangewide status report summarized the
best available information on BCT (May and Albeke 2005, pp. i, 16, 103-
104). The status report was peer reviewed by five recognized experts in
the fields of fishery biology, conservation biology, and genetics. The
peer reviewers found that the status report provided sound scientific
data to use in this 12-month finding.
The 2001 finding on Bonneville Cutthroat Trout included 28,863
hectares (71,322 acres) of lake habitat (indicated as an adfluvial life
history) (USFWS 2001, pp. 34, 44, 50, 75). The 2005 BCT rangewide
status report relied on a protocol that was not designed to address
lake populations; however, 8 lakes connected to occupied stream habitat
were included as 412 stream kilometers (km) (256 stream miles (mi))
(May and Albeke 2005, pp. 107, 110, 120). Thus, throughout the
remainder of the document, all occupied BCT habitat is reported as
stream habitat and includes lake populations. These lake populations
are an important component in conserving BCT, and some lakes are
specifically designated to preserve genetically pure populations
(Donaldson 2008, pp. 8-9).
The BCT Conservation Team's status report included an analysis of
probable historic distribution (May and Albeke 2005, pp. 6, 16-19). Our
understanding of BCT historic distribution is based on habitat thought
to be occupied around 1800. The determination of occupation in this era
was based on historic
[[Page 52238]]
climactic conditions, stream channel gradient, barriers that would
preclude fish, and expertise of fishery biologists familiar with each
watershed. The analysis resulted in 10,876 (km) (6,758 mi) of stream
habitat potentially occupied historically (May and Albeke 2005, pp. 6,
16-19). This analysis included estimated stream miles for historically
occupied BCT lakes because the analysis protocol was not designed to
address lake populations separately. The historically occupied habitat
identified in each State included: Utah--7,916 km (4,919 mi) (73
percent); Idaho--1,854 km (1,152 mi) (17 percent); Wyoming--974 km (605
mi) (9 percent); and Nevada--132 km (82 mi) (1 percent) (May and Albeke
2005, pp. 6, 16-19). The United States is divided and sub-divided into
successively smaller hydrologic units that are classified into four
levels: regions, sub-regions, accounting units, and cataloging units.
Fourth-level hydrologic unit codes (HUCs) in the Lake Bonneville Basin,
including Pine Valley, Tule Valley, Pilot-Thousand Springs, Northern
Great Salt Lake Desert, Lower Beaver, and Sevier Lake, were not
included as historical habitats because they were judged unsuitable due
to extreme conditions, because information on them prior to 1800 is
unavailable, or because historical records indicate that they were
devoid of fish.
Current Distribution
Current distribution of BCT is approximately 3,830 km (2,380 mi)--
35 percent of the probable historically occupied stream miles (May and
Albeke 2005, p. 19). Currently occupied habitat identified in each
State includes Utah--2,438 km (1,515 mi) (64 percent); Idaho--869 km
(540 mi) (23 percent); Wyoming--476 km (296 mi) (12 percent); and
Nevada--47 km (29 mi) (1 percent) (May and Albeke 2005, p. 19).
The BCT is well distributed throughout its range in four watershed-
based GMUs (see Figure 1; Table 1 below). In earlier assessments, five
GMUs or GUs (geographic units) were identified as including current
populations of BCT; however, we combined the Bear Lake and Bear River
GMUs because they occur within one watershed, and our analysis was
conducted by watershed (May and Albeke 2005, pp. 4-5). This
reconfiguration of GMUs does not imply a reduction in the geographic
area where BCT occur (May and Albeke 2005, pp. 2-5).
Within each GMU, streams were identified to the 4th-level
hydrologic unit and assigned to a HUC. BCT occupy habitat in 22 of the
23 HUCs determined to likely have supported historical habitat. BCT
also occupy habitat in three HUCs that are either partially or totally
outside of the subspecies historic range (May and Albeke 2005, pp. 19-
20); most of these populations were reintroduced into suitable habitat
with no record of nonnative fish (Behnke 1992, pp. 134-135). The Bear
River GMU has the greatest extent of currently occupied BCT habitat
(2,010 km/1,249 mi), followed by the Northern Bonneville (1,532 km/952
mi), Southern Bonneville (187 km/116 mi), and the West Desert (101 km/
63 mi).
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Table 1--From May and Albeke 2005, (p. 19), Table 21 (p. 34)
----------------------------------------------------------------------------------------------------------------
Km (mi) occupied
Km (mi) currently Number of BCT by BCT
GMU name occupied by BCT conservation conservation
populations populations
----------------------------------------------------------------------------------------------------------------
Bear River............................................. 2,010 (1,249) 33 1,753 (1,089)
Northern Bonneville.................................... 1,532 (952) 65 1,318 (819)
Southern Bonneville.................................... 187 (116) 21 145 (90)
West Desert............................................ 101 (63) 34 101 (63)
--------------------------------------------------------
Totals............................................. 3,830 (2,380) 153 3,316 (2,061)
----------------------------------------------------------------------------------------------------------------
Hybridization
Hybridization is a concern for many cutthroat trout populations. An
introgressed population results when a nonnative species or subspecies
is introduced into or invades native cutthroat trout habitat, the two
species then interbreed (i.e., hybridize), and the resulting hybrids
survive and reproduce. If the hybrids backcross with one or both of the
parental species, genetic introgression occurs. Continual introgression
can eventually lead to the loss of genetic identity of one or both
parent species, thus resulting in a ``hybrid swarm'' consisting
entirely of individual fish that often contain variable proportions of
genetic material from both of the parental species.
Our criteria for considering the potential impact of introgressed
populations of BCT are consistent with a position paper, titled
``Genetic Considerations Associated with Cutthroat Trout Management,''
developed by the fish and wildlife agencies of the intermountain
western States (UDWR 2000a, pp. 1-9). Signatories to the position paper
include the IDFG, Montana Fish Wildlife and Parks, NDOW, New Mexico
Game and Fish Department, UDWR, and WGFD. The document identified, for
all subspecies of inland cutthroat trout, three tiers of natural
populations for prioritizing conservation and management options under
State fish and wildlife management authorities: (1) Core conservation
populations composed of greater than 99 percent cutthroat trout genes;
(2) conservation populations that generally ``have less than 10 percent
introgression, but in which introgression may extend to a greater
amount depending upon circumstances and the values and attributes to be
preserved''; and (3) cutthroat trout sport fish populations that, ``at
a minimum, meet a species'' phenotypic expression defined by
morphological and meristic characteristics (counts of body parts) of
cutthroat trout.''
The premise of the position paper on genetic considerations was
that populations must conform, at a minimum, to the morphological and
meristic characteristics of a particular cutthroat trout subspecies in
order to be included in a State's conservation and management plan for
that subspecies. Conservation populations of a cutthroat trout
subspecies include fish believed to have uncommon or important genetic,
behavioral, or ecological characteristics relative to other populations
of the subspecies. Sport fish populations, conversely, while conforming
morphologically (and meristically) to the scientific taxonomic
description of the subspecies, do not meet the additional genetic
criteria of conservation or core, and are managed for their value as
sport fish rather than for conservation of the subspecies.
Following the State management agencies' position paper (UDWR
2000a, pp. 1-9), a ``core population'' is genetically unaltered (pure),
and a ``conservation population'' is pure (a core population) or
slightly introgressed (typically less than 10 percent) due to past
hybridization, yet has attributes worthy of conservation. Therefore,
conservation populations include both core populations (genetically
pure) and populations that are less than 10 percent introgressed with
rainbow trout or other subspecies of cutthroat trout (May and Albeke
2005, p. 71). The BCT rangewide status report (May and Albeke 2005, p.
31) identified 153 stream populations (3,316 km/2,061 mi) as
conservation populations (see Table 1, above, and Figure 2). Of the 153
conservation populations, 73 (732 km/455 mi) are considered core
populations containing genetically pure BCT.
We consider all core and conservation populations, as defined under
the States' standards and as described by May and Albeke (2005, p. 31),
for purposes of conducting this status review. Because the categories
are nested (conservation populations include core populations), we
refer to them collectively as ``BCT conservation populations'' in the
remainder of this finding. Some of the data presented in May and Albeke
(2005) pertains to all BCT populations (including sport fish) or
habitat. Those areas of this document that do not specify
``conservation populations,'' therefore, are referring to all BCT
populations. We conducted our analysis on conservation populations
because we found that BCT with less than 10 percent introgression still
express important behavioral, life history, or ecological adaptations
of indigenous populations within the range of the subspecies, and
remain valuable to the overall conservation and survival of the
subspecies (Campton and Kaeding 2005, pp. 1323-1325). (See also Factor
E, Hybridization with Nonnative Fishes.)
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Conservation Populations
Designated BCT conservation populations exist throughout the
subspecies' historic range (May and Albeke 2005, p. 31)--in all four
States and in the four designated GMUs. BCT currently occupy some
habitat in 22 of the 23 HUCs historically occupied, and BCT that meet
the conservation population definition (less than 10 percent
introgressed) exist in 19 of those HUCs. BCT conservation populations
were also identified in two HUCs (Spring-Steptoe and Hot Creek-Railroad
Valley) outside historic range, and three additional conservation
populations were identified outside historical range within the Upper
Virgin HUC. The majority of conservation populations (65) occur in the
Northern Bonneville GMU occupying 1,318 km (819 mi). The remainder of
BCT conservation populations are relatively equally distributed among
the West Desert (34), Bear River (33), and Southern Bonneville (21)
GMUs. These populations occupy 101 km (63 mi), 1,753 km (1089 mi), and
145 km (90 mi) respectively (May and Albeke 2005, p. 34).
The majority of BCT conservation populations (101; 66 percent)
occur as isolated, non-networked populations (May and Albeke 2005, p.
34); 25 populations (16 percent) are weakly connected; 15 populations
(10 percent) are moderately connected; and 12 populations (8 percent)
have migratory forms and open migration corridors that make them
strongly connected. The strongly connected populations occur in Utah,
Idaho, and Wyoming in the Bear River Geographic Management Unit (GMU)
and Northern Bonneville GMU (May and Albeke 2005, pp. 34, 107, 115,
117).
BCT Population Trend
BCT population trend and status can be interpreted from results of
previous assessments conducted from the early 1970's through the
present time. Hickman (1978, pp. 121-122) identified approximately 15
populations he considered ``pure'' occupying approximately 34 km (21
mi) of stream habitat. Duff (1988, pp. 121-127) reported 41
``genetically pure'' BCT populations (39 stream populations) in
association with 304 km (189 mi) of stream habitat. A draft Service
status review that was never finalized reported 48 genetically pure BCT
populations throughout the Bonneville Basin (USFWS 1993, pp. 1-62).
Duff (1996, pp. 38-39) further refined his BCT population distribution
reporting 81 genetically ``pure'' populations occupying 377 km (234 mi)
of stream habitat. A Service status review found that BCT occupied a
total of 1,372 km (852 mi) of stream habitat and 28,352 ha (70,059
acres) of lake habitat totaling 291 populations (USFWS 2001, pp. iv-v).
BCT assessments conducted between 1978 and 1996 generally counted
populations that were thought to be genetically ``pure.'' The 2001
Service assessment determined the genetic status of each population but
was more inclusive and counted management, conservation, and potential
conservation populations (USFWS 2001, pp. viii-xi). The May and Albeke
(2005) assessment assessed the genetic status of each BCT population
and then categorized genetic status based on the criteria in the
State's genetic position paper (UDWR 2000a, pp. 1-9).
Methods for tallying the number of individual BCT populations
tended to vary by individual assessment, with earlier assessments
tending to split tributary populations from mainstem river reaches. In
contrast, methods used for the May and Albeke (2005, p. 64) assessment
tended to group populations by higher order streams, thereby reducing
the total count of populations. Thus, it is important to consider
changes in the amount of occupied habitat when assessing population
trends from different assessments rather than to simply rely on changes
in number of populations. The number of known stream miles occupied by
BCT conservation populations increased over time from 15 populations in
34 km (21 mi) of habitat in 1978 to 153 populations in 3,316 km (2,061
mi) in 2004. Some of the increase in BCT conservation populations and
their habitat is the result of conservation actions such as the
discovery of more populations in recent years; the expansion or
restoration of populations; and the eligibility of populations for
conservation status (through genetic testing) that were previously
considered hybridized. Increases in the amount of BCT conservation
population habitat is also due to the use of a more accurate GIS-based
assessment method that incorporated the National Hydrography Dataset
geodatabase (May and Albeke 2005, p. 2) and also the inclusion of lakes
as river miles as used in the most recent assessment protocol (see
above), although the increase due to the inclusion of lakes in the
river mile calculation only accounts for an additional 412 km (256 mi)
of stream habitat.
The BCT Conservation Team's most recent analysis of the number of
BCT conservation populations and the extent of their habitat indicates
that conservation populations have increased from 153 populations in
3,316 km (2,061 mi) in 2004 (May and Albeke 2005, p. 31), to 172
populations in 3,333 km (2,071 mi) in 2008 (Burnett 2008a, entire).
This most recent evaluation of the BCT Conservation Team's database was
cursory and was not performed for other population parameters discussed
in May and Albeke (2005) (i.e., restoration activities, genetic status,
population health and densities, etc.); however, it does indicate that
the number of BCT conservation populations and their habitat continue
to increase.
Summary of Factors Affecting the Species
Section 4 of the Act (16 U.S.C. 1533), and implementing regulations
at 50 CFR 424, set forth procedures for adding species to the Federal
Lists of Endangered and Threatened Wildlife and Plants. In making this
finding, we summarize information regarding the threats to the BCT in
relation to the five factors provided in section 4(a)(1) of the Act.
In making this finding, we considered all scientific and commercial
information that we received or acquired up to the publication of the
2001 12-month finding (66 FR 51362), and after publication of the
notice initiating this finding (73 FR 7236; February 7, 2008). We
relied primarily on published and peer-reviewed documentation for our
conclusions, and most significantly, the rangewide status report
competed by the BCT Conservation Team (May and Albeke 2005, entire).
Pursuant to section (4) of the Act, a species may be determined to
be an endangered or threatened species on the basis of any of the
following five factors: (A) Present or threatened destruction,
modification, or curtailment of habitat or range; (B) overutilization
for commercial, recreational, scientific, or educational purposes; (C)
disease or predation; (D) inadequacy of existing regulatory mechanisms;
or (E) other natural or manmade factors affecting its continued
existence. We evaluated whether threats to the BCT may affect its
survival. Our evaluation of threats, based on the best scientific and
commercial information available, is presented below.
Factor A. The Present or Threatened Destruction, Modification, or
Curtailment of the Species' Habitat or Range
Land use activities associated with each BCT conservation
population were
[[Page 52243]]
identified and documented in May and Albeke (2005, p. 52, Table 30),
but the significance of the activities was not determined in relation
to individual populations or to the conservation of the subspecies.
Non-angling recreation (camping, hiking, ATV use, etc.) occurs in 69
percent of the conservation populations. Livestock grazing occurs in 58
percent of the conservation populations, roads in 69 percent, timber
harvest in 20 percent, and dewatering in 30 percent. Hydroelectric
plants, water storage, or flood control occurs in 20 percent of the
conservation populations. A small percentage of populations have mining
or nonnative fish stocking. Many populations have more than one land
use occurring in the area.
A comprehensive assessment of the effects of land management
practices on BCT does not exist. However, an evaluation of habitat
quality was conducted for currently occupied habitat (May and Albeke
2005, p. 26). The evaluation considered both natural habitat features
and human-caused disturbances. A stream ranked as ``excellent'' if it
had ample pool habitat, low sediment levels, optimal temperatures, and
quality riparian habitat. A ``good'' habitat quality rating indicated
the presence of some less than ideal attributes, and ``fair'' indicated
the presence of a greater number of less than ideal attributes. A
``poor'' habitat quality rating indicated the inferior conditions of
most habitat attributes. Of total occupied habitat for all BCT
populations, excellent habitat conditions occurred in approximately 196
km (122 mi) (5 percent); good conditions occurred in 1,801 km (1,119
mi) (47 percent); fair conditions occurred in 1,080 km (671 mi) (28
percent); poor conditions occurred in 628 km (390 mi) (16 percent), and
unknown conditions occurred in 126 km (78 mi) (3.2 percent). The
majority of occupied habitat (80 percent) is in fair, good, or
excellent condition.
Livestock grazing occurs in 58 percent of the BCT populations.
Livestock grazing became an acute problem for watershed health in the
late 1880s through 1930s when grazing, particularly sheep grazing, was
so extensive and ill-managed that widespread watershed damage occurred
throughout many areas in the Bonneville Basin. In fact, at the turn of
the century, sheep were crowding cattle out of many areas (Peterson and
Speth 1980, p. 179). In the Wasatch Mountains east of Salt Lake City,
Utah, over-grazing of sheep denuded mountain meadows, some to the
extent that watersheds experienced massive soil loss, land-slides and
severe erosional damage. In addition to resident sheep, Utah was at a
geographical `crossroads of the west' where hundreds of sheep were
trailed to and from neighboring States (Peterson and Speth 1980, p.
179).
Overgrazing by sheep can be particularly damaging to overall
watershed conditions. Sheep have been known to graze vegetation down to
dirt and ``grub'' away at grass roots thereby damaging the soil mantle,
which acts to hold water for plant uptake (Peterson and Speth 1980,
p.180). The extensive watershed damage typical of over-grazing sheep in
the early 20th century led to massive soil erosion, land slides, and
flooding during heavy precipitation (Cottam 1947, pp. 23-29). Such
events can completely eliminate local fish populations and undoubtedly
affected local populations of BCT. For streams already fragmented from
diversions or dewatering, such events could have led to local
extirpation of BCT where no connected populations were available to
recolonize streams after a catastrophic flood.
Although cattle grazing can affect watershed conditions as well,
the greater concern for cattle grazing stems from direct stream impacts
where cattle are permitted to dwell in or are trailed through stream
channels and riparian areas. Without adequate management, cattle can
trample and destroy instream habitat and stream banks. They forage on
lush riparian vegetation, which leads to degraded stream conditions and
changes in channel morphology. Trampling destroys undercut banks
resulting in wider and shallower channel morphology. Where this occurs,
BCT can be impacted by increased water temperatures, loss of habitat
complexity, altered macroinvertebrate food-base, and increased
deposition of fine sediment (Platts 1991, p.393; Belsky et al. 1999,
p.420; Rinne 1999, p.14).
When livestock grazing is managed appropriately, it can occur in
the vicinity of stream and riparian habitat, and habitat conditions
that support fish populations can still be maintained (Fitch and Adams
1998, p. 197). The Western Watersheds Project, Inc. (Carter 2008, pp.
1-7) submitted information documenting grazing impacts in localized
areas in the Bear River GMU. Much of the information documents range
conditions relative to grazing allotment reauthorizations. The
information and conclusions presented included the assumption that, if
a land management activity occurred within the vicinity of a BCT
population, it was adversely affecting the population. We recognize
that overgrazing can cause adverse impacts to individual populations of
BCT. However, only 16 percent of the occupied stream miles have poor
habitat quality (May and Albeke 2005, p. 26). Specific information on
grazing impacts to BCT habitat on a rangewide basis is not available.
We found no information indicating that overgrazing significantly
affects the rangewide status of BCT now, or will do so in the
foreseeable future. Therefore, we conclude that overgrazing is not a
significant threat to BCT.
Roads, timber harvest, and dewatering occur in the area of some BCT
populations. Similar to water development and grazing, the greatest
impacts from timber harvesting occurred from 1850 to 1950. Although
timber harvesting still occurs on National Forest Lands and very
limited private lands in the Bonneville Basin, and may have some
detrimental impacts on streams and watersheds, timber harvesting
standards have substantially improved, particularly regarding
protection of streams and watershed condition, and the catastrophic
destruction that occurred in the first 100 years of pioneer settlement
no longer occurs.
Currently, timber harvesting affects BCT through the indirect
effects of road building and deforestation. Road building is known to
add fine sediment to streams where roads cross or follow stream
channels. These fine sediments can fill interstitial spaces important
for successful spawning and survival of eggs and larval fish as well as
alter the macro-invertebrate food base (Williams and Mundie 1978,
p.1032-1033). Deforestation can also add sediment input into streams
where riparian buffers are not implemented. Loss of trees also
increases water volume draining into stream channels, which can alter
flow and sediment regimes or exacerbate catastrophic flooding during
extreme precipitation events.
Within the Bonneville Basin, timber harvesting is fairly limited
compared to other areas of the inland west, mainly because the arid
climate is not conducive to extensive, lush forests. Timber harvest
occurs in only 20 percent of BCT conservation population habitat (May
and Albeke 2005, p. 52, Table 30). We found no information indicating
that timber harvesting significantly affects the rangewide status of
BCT now, or will do so in the foreseeable future. Therefore, we
conclude that timber harvesting is not a significant threat to BCT.
Direct effects of water diversions and depletions (dewatering) on
BCT occur where reaches are dewatered or made inaccessible by instream
barriers. Secondary effects of water development may include higher
water temperatures
[[Page 52244]]
in summer months because of lower water volume and diminished riparian
condition and altered instream and shoreline habitat, all of which can
impact cutthroat trout spawning and populations (Clancy 1988, pp. 40-
41). Dewatering occurs in only 30 percent of BCT conservation
population habitat (May and Albeke 2005, p. 52, Table 30). Rates of
habitat loss through water diversions and depletions were likely
heaviest for the decades immediately after pioneer settlement, in the
late 1800s, throughout the Bonneville Basin near locations of
population growth. We found no information indicating that dewatering
significantly affects the rangewide status of BCT now, or will do so in
the foreseeable future. Therefore, we conclude that dewatering is not a
significant threat to BCT.
Idaho and Nevada have no producing oil or gas wells in BCT areas.
However, oil and gas development has been accelerating over the last
several years in Utah and Wyoming. Oil and gas development could affect
BCT through increased land disturbance from roads and pads that could
cause water quality problems associated with increased sediment loads,
and through leaks, spills, and discharge of produced water reaching BCT
habitat (WGFD 2004, pp. 25-26). The BLM and Utah Division of Oil Gas
and Mining provided information on locations of existing active and
inactive wells and oil and gas leases on BLM, USFS, and other lands
where BLM has jurisdiction over the subsurface mineral rights within
the BCT range in Utah and Wyoming (BLM 2008a, entire; UDOGM 2008,
entire). A well exists within 1.6 km (1 mi) or less of 26 BCT
conservation populations (17 percent of all conservation populations).
Of these 26 populations, 2 were near active or producing wells; the
wells near the remaining 24 populations were non-producing and were
shut-in, plugged and abandoned, or abandoned entirely for development.
These non-producing wells have a greatly reduced likelihood of
releasing oil and gas related contaminants into BCT habitat (BLM 2008b,
entire). Relatively little overlap exists between oil and gas
development sites and BCT conservation populations. BCT populations
typically occur at higher elevations where minimal oil and gas activity
exists. An analysis of potential future oil and gas development for the
States of Wyoming and Utah indicates that the majority of leases occur
outside the historic range of BCT (BLM 2008b, entire). Potential
impacts to BCT resulting from oil and gas development on Federal land
are typically assessed through the National Environmental Policy Act
(NEPA) review process; as a result, future effects should be disclosed
and effects to BCT will have to be taken into consideration due to the
sensitive species management status of BCT on Federal land. Therefore,
based on the best scientific and commercial information available, we
conclude that dewatering is not a significant threat to BCT now, or in
the foreseeable future.
Summary of Factor A
Land use practices, such as livestock grazing, road construction
and maintenance, dewatering, and timber harvest, are occurring to some
extent in most areas of occupied habitat. However, habitat quality
ratings are fair, good, or excellent in 80 percent of BCT habitat
throughout the current range of the subspecies. Approximately half of
all BCT populations (49 percent) occur on Federal lands where land use
regulations are in place to ensure ongoing maintenance of existing
habitat (see Factor D). Restoration and conservation activities are
occurring for at least 57 percent of the conservation populations.
We find that the presence alone of an activity within a stream
segment containing a conservation population is not sufficient evidence
to conclude that the population is threatened or that a certain land
use activity affects all populations rangewide at a significant level.
Additional parameters, such as magnitude of impacts, distribution and
abundance of BCT populations, and population trends, lend to an overall
status determination. Many species exist in managed landscapes; not all
are significantly impacted by human-caused influences to the level of
being considered threatened under the Act.
BCT conservation populations are well distributed in four GMUs,
collectively forming a solid basis for persistence of BCT. These GMUs
contain 19 of the 23 HUCs determined to have supported historical BCT
habitat. In addition, BCT conservation populations currently occupy
habitat in three HUCs that are either partially or totally outside the
subspecies' historic range.
Based on the best scientific and commercial information available,
we conclude that BCT is not now or in the foreseeable future,
threatened by destruction, modification, or curtailment of its habitat
or range to the extent that listing under the Act as a threatened or
endangered species is warranted at this time.
Factor B. Overutilization for Commercial, Recreational, Scientific, or
Educational Purposes
No commercial harvest of BCT currently occurs, so only recreational
angling could potentially result in overutilization. Data show that
angling occurs in 60 percent of BCT conservation populations (May and
Albeke 2005, p. 52). Utah, Idaho, and Wyoming have special regulations
providing protection against over-harvest of BCT. These special
regulations include catch-and-release requirements, limited harvest,
fishing closures, and tackle restrictions. In addition, the remote
location of many BCT streams provides protection from heavy fishing
pressure (NDOW 2006, p. S-28; Baker et al. 2008, p. 29; Donaldson 2008,
p. 3).
The State of Idaho implements several fishing regulations to manage
potential angler impacts in State waters. For most streams able to
support larger fish, bag limits are 2 fish greater than or equal to 40
centimeters (cm) (16 in) in length. In smaller streams, where BCT
typically do not exceed 30 cm (12 in), the general stream limit is 2
fish, and no size constraints exist. In other waters, seasonal angling
restrictions or catch-and-release-only regulations are implemented
(IDFG 2008, pp. 3, 19). In Utah, several fishing regulations protect
native cutthroat trout from overutilization. The State reduced trout
bag and possession limits from eight fish to four, and imposed short-
term fishing closures to protect native cutthroat trout (Donaldson
2008, p. 3). Wyoming implements angling restrictions, such as size
limits, reduced bag limits, and tackle restrictions to protect BCT
populations (WGFD 2008, p. 8). Many of Nevada's BCT populations occur
in remote areas, which provide protection from heavy fishing pressure
(Baker et al. 2008, p. 29). None of the four States considers angling,
under their current regulations, to be a threat to the subspecies.
Collection of BCT for scientific or educational purposes is
controlled by strict State permitting processes that prevent excessive
sampling throughout its range in Utah, Wyoming, Idaho, and Nevada.
Collection of fish tissue for genetic sampling is conducted by
nonlethal techniques (Rogers 2007, pp. 1-3).
Summary of Factor B
No commercial harvest of BCT currently occurs. Only recreational
angling could potentially result in overutilization. However, Utah,
Idaho, and Wyoming have special regulations
[[Page 52245]]
providing protection against over-harvest of BCT. Also, in our 2001 12-
month finding (66 FR 51362), we concluded that angler harvest did not
pose a significant threat to the continued existence of BCT, and we
know of no new information during development of this finding to change
this conclusion. Collection of BCT for scientific or educational
purposes is controlled by strict State permitting processes throughout
the range of the subspecies. Therefore, we conclude that the best
scientific and commercial information available indicates that
overutilization for commercial, recreational, scientific, or
educational purposes is not a significant threat to BCT now, or in the
foreseeable future.
Factor C. Disease or Predation
Disease
The BCT Conservation Team evaluated disease in the BCT status
report (May and Albeke 2005, pp. 11-12, 40-42). Diseases considered had
the potential to cause significant impacts to population health and
included, but were not limited to, whirling disease, infectious
pancreatic necrosis virus, and furunculosis. The BCT Conservation Team
assessed risks based on proximity of disease-causing pathogens and
their accessibility to a population. The majority of the populations
(63 percent) have limited risk because disease and pathogens are not
known to exist in the watershed, or a barrier blocks upstream fish
movement. In general, isolated populations have less risk of
catastrophic diseases. Fourteen populations (9 percent) are currently
known to be infected with one of the identified diseases (May and
Albeke 2005, pp. 40-41).
In recent years, whirling disease has become of great concern to
fishery managers in western States. Whirling disease is caused by the
nonnative myxosporean parasite, Myxobolus cerebralis. This parasite was
introduced to the United States from Europe in the 1950's and requires
two separate host organisms to complete its life cycle. Its essential
hosts are a salmonid fish and an aquatic worm, Tubifex tubifex.
Juvenile, sub-adult, and adult life stages of BCT have been shown to be
susceptible to whirling disease in the Logan River, and some Logan
River study sites exhibit a downward trend in BCT abundance (Budy et
al. 2005, pp. xi-xiii). Despite this, BCT in the Logan River
demonstrate high growth and survival rates and are generally in
relatively good health. Logan River tributaries are important refuges
from whirling disease-infected areas in the Logan mainstem (Budy et al.
2005, pp. xi-xiii). Tubifex tubifex is most abundant in areas of high
sedimentation, warmer water temperatures, and low dissolved oxygen.
Most populations of BCT occur in cold water stream habitats at high
elevations, where Tubifex tubifex is less likely to be abundant.
All four States have developed management activities to protect BCT
populations from whirling disease. Though whirling disease is known to
occur in some Nevada waters, it currently does not pose a threat to BCT
populations because it occurs at low levels among BCT populations (NDOW
2006, pp. S27). Regardless, Nevada is in the process of formalizing
protocols for BCT reintroductions and transplants relating to disease
certification and broodstock management (NDOW 2006, pp. S27, S32).
Idaho has outlined several strategies to protect BCT populations from
the negative effects of disease. Strategies include monitoring fish
populations for disease, prohibiting importation of fish and wildlife
that carry disease risk, and ensuring that stocking, translocation, and
propagation of fish do not contribute to the transmission or
introduction of diseases (IDFG 2008, p. 14). Utah has some of the most
stringent fish disease laws in the United States, which do not allow
the stocking of fish that test positive for whirling disease (Donaldson
2008, pp. 4-5). UDWR is studying the effects of whirling disease in a
portion of BCT occupied waters in Utah that have been infected
(Donaldson 2008, p. 4). Wyoming has a policy of not stocking fish that
test positive for Myxobolus cerebralis (WGFD 2008, p. 9).
Predation
Of the 153 conservation populations identified in the rangewide BCT
status report, 97 (63 percent) had no interaction with nonnative fish
and 56 (37 percent) were sympatric with nonnative fish (May and Albeke
2005, p. 31). All BCT conservation populations sympatric with nonnative
fish are located in the Bear River and Northern Bonneville GMUs. In
these GMUs, BCT can be replaced by nonnative trout, but the degree to
which predation is a factor in this replacement has not been well
documented (Holden et al. 1997, pp. 3-21). Although nonnative fish can
have negative effects on BCT in localized areas due to predation,
research in the Logan River drainage shows that it is possible for BCT
populations to persist in the presence of predacious nonnative fish
(Behnke 1992, p. 107; Budy et al. 2005, pp. xi-xiii).
Predation can affect BCT, mainly during early life stages, where
other predaceous fish occupy the same area (UDWR 2000b, p. 48). Utah
has implemented several management actions intended to alleviate
potential predation of BCT by nonnative trout, including: nonnative
removal/barrier installation projects; barring nonnative cutthroat
stocking in conservation drainages; increasing angler harvest limits
for brook trout in the Boulder and Uinta Mountains; and initiating
fisheries research work (Donaldson 2008, pp. 5-7). Nevada has virtually
eliminated threats to BCT from nonnative fish by utilizing barriers and
nonnative removal restoration projects (Baker et al. 2008, pp. 3-5;
NDOW 2006, p. S-27).
Similar to Utah, Idaho and Wyoming have enacted management actions
intended to alleviate potential predation of BCT by nonnative trout.
Idaho has discontinued stocking brook trout into native trout streams,
increased the daily limit for brook trout from 6 to 25, and removed or
suppressed nonnative trout species that compete with BCT (IDFG 2008,
pp. 6-7). Wyoming is monitoring BCT populations to ensure that
nonnative populations do not become established in new waters in the
Bear River drainage, have ceased stocking nonnative trout in waters
managed for BCT conservation populations, and have implemented
nonnative removal/barrier installation projects to control nonnative
fish in BCT habitat (Emmrich 2008, p. 2; WGFD 2008, p. 10).
Summary of Factor C
Only 14 (9 percent) BCT conservation populations are infected with
a significant disease, and no additional populations are at high risk
for infection (May and Albeke 2005, pp. 40-41). Therefore, we conclude
that the best scientific and commercial information available indicates
that neither whirling disease nor other disease organisms significantly
threaten BCT now, or in the foreseeable future.
Predation by nonnative fish, the primary source of predation on
young BCT, may have some effect on BCT populations in the Bear River
and Northern Bonneville GMUs. However, 63 percent of conservation
populations have no interactions with nonnative fish. Also, research
shows that it is possible for BCT populations to persist in the
presence of predacious nonnative fish (Behnke 1992, p. 107; Budy et al.
2005, pp. xi-xiii). State fish and wildlife agencies continue to
implement management actions intended to alleviate potential predation
of BCT by nonnative fish. At this time, we know of
[[Page 52246]]
no information that indicates to us that predation significantly
affects BCT now, or in the foreseeable future.
Factor D. Inadequacy of Existing Regulatory Mechanisms
The Act requires us to examine the adequacy of existing regulatory
mechanisms with respect to extant threats that place the subspecies in
danger of becoming either threatened or endangered. Regulatory
mechanisms affecting BCT fall into three general categories: angling,
land management, and water quantity.
Angling
The States of Utah, Idaho, Nevada, and Wyoming consider BCT a game
species, and each State has specific regulations regarding catching BCT
by angling. We concluded above that recreational angling is not a
significant threat to BCT, now or in the foreseeable future (see Factor
B).
Regulatory Mechanisms Involving Land Management
Numerous State and Federal laws and regulations help reduce adverse
effects of land management activities on BCT. Most habitat in
watersheds inhabited by BCT conservation populations is managed by
Federal land management agencies, primarily the USFS and BLM, and to a
limited extent the NPS. Federal laws that reduce impacts to BCT and
their habitats include the Clean Water Act, Federal Land Policy and
Management Act, National Forest Management Act, Wilderness Act, and
National Environmental Policy Act. Approximately 49 percent of all
occupied BCT habitat (including both sport fish and conservation
populations) occurs on lands managed by Federal agencies, and the USFS
manages the majority (May and Albeke 2005, p. 29). Of the 3,830 km
(2,380 mi) of occupied habitat, 1,867 km (1,160 mi) are under Federal
jurisdiction and the majority occur on National Forests (1,209 km (751
miles)) (May and Albeke 2005, p. 29); these figures include sport fish
populations because figures for conservation populations alone are not
available (see Table 2 below). BCT occur in a large geographic area
within the following National Forests: Bridger-Teton, Caribou-Targhee,
Dixie, Fishlake, Humboldt-Toiyabe, Uinta, and Wasatch-Cache. BCT occupy
11 km (7 mi) of land administered by the BLM, and 7 km (4.4 mi) managed
by the NPS. Approximately 657 km (408 mi) of occupied BCT habitat
occurs in wilderness areas managed by the USFS or BLM. Wilderness Areas
and National Parks provide an extra level of protection for BCT because
many land management activities are prohibited in them.
Table 2--BCT Occupied Land Ownership
[Numbers include areas occupied by both sport fish and conservation populations]
----------------------------------------------------------------------------------------------------------------
USFS and BLM
USFS BLM NPS Wilderness Non-federal Total
----------------------------------------------------------------------------------------------------------------
1,209 km........................ 11 km 7 km 657 km 2,603 km 3,830 km
(751 mi)........................ (7 mi) (4.4 mi) (408 mi) (1,618 mi) (2,380 mi)
----------------------------------------------------------------------------------------------------------------
U.S. Forest Service
The USFS Sensitive Species Policy in Forest Manual 2670 outlines
procedures for conserving sensitive species. The policy applies to
projects implemented under the