Endangered and Threatened Wildlife and Plants; 12-Month Finding on a Petition to List the Least Chub as Threatened or Endangered, 35398-35424 [2010-15070]
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Services Field Office (see ADDRESSES);
by telephone at (801) 975-3330; or by
facsimile at (801) 975-3331. Persons
who use a telecommunications device
for the deaf (TDD) may call the Federal
Information Relay Service (FIRS) at 800877-8339.
SUPPLEMENTARY INFORMATION:
DEPARTMENT OF THE INTERIOR
Fish and Wildlife Service
50 CFR Part 17
[Docket No. FWS-R6-ES-2008-0088]
[MO 92210-0-0008-B2]
Endangered and Threatened Wildlife
and Plants; 12-Month Finding on a
Petition to List the Least Chub as
Threatened or Endangered
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AGENCY: Fish and Wildlife Service,
Interior.
ACTION: Notice of 12-month petition
finding.
SUMMARY: We, the U.S. Fish and
Wildlife Service (Service), announce a
12–month finding on a petition to list
the least chub (Iotichthys phlegethontis),
a fish, as threatened or endangered and
to designate critical habitat under the
Endangered Species Act of 1973, as
amended (Act). After review of all
available scientific and commercial
information, we find that listing the
least chub as threatened or endangered
under the Act is warranted. Currently,
however, listing the least chub is
precluded by higher priority actions to
amend the Lists of Endangered and
Threatened Wildlife and Plants. Upon
publication of this 12-month petition
finding, we will add the least chub to
our list of candidate species with a
listing priority number (LPN) of 7. We
will develop a proposed rule to list this
species as our priorities and funding
allow. We will make any determination
on critical habitat during development
of the proposed listing rule. In the
interim, we will address the status of
the candidate taxon through our annual
Candidate Notice of Review (CNOR).
DATES: This finding was made on June
22, 2010.
ADDRESSES: This finding is available on
the Internet at https://
www.regulations.gov at Docket Number
FWS-R6-ES-2008-0088 and https://
www.fws.gov/mountain-prairie/species/
fish/leastchub. 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 Field Office, 2369 West Orton
Circle, Suite 50, West Valley City, UT
84119. Please submit any new
information, materials, comments, or
questions concerning this finding to the
above address.
FOR FURTHER INFORMATION CONTACT:
Larry Crist, Field Supervisor, U.S. Fish
and Wildlife Service, Utah Ecological
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Background
Section 4(b)(3)(B) of the Act (16
U.S.C. 1531 et seq.), requires that, for
any petition to revise the Federal Lists
of Threatened and Endangered Wildlife
and Plants that contains substantial
scientific or commercial information
indicating that listing the species may
be warranted, we make a finding within
12 months of the date of receipt of the
petition. In this finding, we determine
that the petitioned action is: (a) Not
warranted, (b) warranted, or (c)
warranted, but 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 Federal Lists of Endangered and
Threatened Wildlife and Plants. Section
4(b)(3)(C) of the Act requires that we
treat a petition for which the requested
action is found to be warranted but
precluded as though resubmitted on the
date of such finding, that is, requiring a
subsequent finding to be made within
12 months. We must publish these 12–
month findings in the Federal Register.
Previous Federal Actions
In 1980, the Service reviewed the
status of the least chub and determined
that there was insufficient data to
warrant its listing as an endangered or
threatened species under the Act. On
December 30, 1982, we classified the
least chub as a Category 2 Candidate
Species (47 FR 58454). Category 2
included taxa for which information in
the Service’s possession indicated that a
proposed listing rule was possibly
appropriate, but for which sufficient
data on biological vulnerability and
threats were not available to support a
proposed rule. In 1989, we conducted a
new status review, and reclassified the
least chub as a Category 1 Candidate
Species (54 FR 554). Category 1
included taxa for which the Service had
substantial information in our
possession on biological vulnerability
and threats to support preparation of
listing proposals. The Service ceased
using category designations in February
1996. On September 29, 1995, we
published a proposed rule to list the
least chub as endangered with critical
habitat (60 FR 50518). A listing
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moratorium, imposed by Congress in
1995, suspended all listing activities
and further action on the proposal was
postponed.
During the moratorium, the Service,
Utah Division of Wildlife Resources
(UDWR), Bureau of Land Management
(BLM), Bureau of Reclamation (BOR),
Utah Reclamation Mitigation and
Conservation Commission (URMCC),
Confederated Tribes of the Goshute
Reservation, and Central Utah Water
Conservancy District (CUWCD)
developed a Least Chub Conservation
Agreement and Strategy (LCCAS), and
formed the Least Chub Conservation
Team (LCCT) (Perkins et al. 1998,
entire). The goals of the LCCAS are to
ensure the species’ long–term survival
within its historic range and to assist in
the development of rangewide
conservation efforts. The objectives of
the LCCAS are to eliminate or
significantly reduce threats to the least
chub and its habitat, to the greatest
extent possible, and to ensure the
continued existence of the species by
restoring and maintaining a minimum
number of least chub populations
throughout its historic range. The LCCT
implements the LCCAS and monitors
populations, threats, and habitat
conditions. The LCCAS was updated
and revised in 2005 (Bailey et al. 2005,
entire).
As a result of conservation actions
and commitments made by signatories
to the 1998 LCCAS (Perkins et al. 1998,
p. 10), measures to protect the least
chub were developed and implemented.
Consequently, we withdrew the listing
proposal on July 29, 1999 (64 FR 41061).
On June 25, 2007, we received a
petition dated June 19, 2007, from
Center for Biological Diversity,
Confederated Tribes of the Goshute
Reservation, Great Basin Chapter of
Trout Unlimited, and Utah Chapter of
the Sierra Club requesting that the least
chub be listed as threatened under the
Act and critical habitat be designated.
Included in the petition and supplement
was supporting information regarding
the species’ taxonomy and ecology,
historical and current distribution,
present status, and actual and potential
causes of decline. We acknowledged the
receipt of the petition and supplement
in a letter to Center for Biological
Diversity, Confederated Tribes of the
Goshute Reservation, Great Basin
Chapter of Trout Unlimited, and Utah
Chapter of the Sierra Club, dated July
13, 2007. In that letter, we also stated
that because of staff and budget
limitations, it was not practical for us to
begin processing the petition at that
time. Based on the population status
and alleged threats described in the
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petition, we found no compelling
evidence to support an emergency
listing at that time.
Funding became available to begin
work on the 90–day finding in Fiscal
Year (FY) 2008. On October 15, 2008,
we published a 90–day finding that the
petitioners provided substantial
information indicating that the species
may be warranted for listing under the
Act, initiated the 12–month finding, and
opened a 60–day public comment
period (73 FR 61007). This notice
constitutes the 12–month finding on the
June 19, 2007, petition to list the least
chub as threatened or endangered.
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Species Information
Taxonomy and Species Description
The least chub (Iotichthys
phlegethontis) is an endemic minnow
(Family Cyprinidae) of the Bonneville
Basin in Utah. Historically, ancient
lakes Bonneville and Provo largely
covered the Bonneville Basin, but over
the past 16,000 years (since the
Pleistocene period), these lakes receded,
leaving behind the current hydrology of
the area (Currey et al. 1984, p. 1). Least
chub likely persisted in peripheral
freshwater sources to the receding lakes
and were widely distributed in a variety
of the resulting habitat types, including
rivers, streams, springs, ponds, marshes,
and swamps (Sigler and Miller 1963, p.
91).
The species’ taxonomic classification
has evolved over time, as described in
the 1995 proposed rule (60 FR 50518).
The least chub is currently classified
within the monotypic genus (containing
only one species) Iotichthys (Jordan et
al. 1930, in Hickman 1989, p. 16; Robins
et al. 1991, p. 21).
As implied by its common name, the
least chub is a small fish less than 55
millimeters (2.1 inches) long, identified
by an upturned or oblique mouth, large
scales, and the absence of an incomplete
lateral line (rarely with one or two
pored scales) (Sigler and Sigler 1987, p.
182). It has a deeply compressed body,
with the front–most part of the dorsal
fin (on the back) lying behind the
insertion of the pelvic fin (on the
underside of the body), and a slender
caudle peduncle (area connecting tail
fin to the body) (Sigler and Miller 1963,
p. 83). Dorsal fin rays number eight
(rarely nine), and anal fin rays also
number eight (Sigler and Miller 1963, p.
83). The pharyngeal teeth (located near
the pharynx) are in two rows (Sigler and
Miller 1963, p. 83).
The least chub is a colorful species.
Individuals have a gold stripe along
blue sides with white to yellow fins
(Sigler and Sigler 1987, p. 182).
Spawning males are olive–green above,
steel–blue on the sides, and have a
golden stripe behind the upper end of
the gill opening (Sigler and Sigler 1987,
p. 182). The fins are lemon–amber, and
sometimes the paired fins are bright
golden–amber (Sigler and Sigler 1987, p.
182). Females and young are pale olive
above, silvery on the sides, and have
watery–white fins; their eyes are silvery,
with a little gold coloration (Sigler and
Sigler 1987, p. 182).
Life History
Sigler and Sigler (1987, p. 183)
considered the least chub to be a slow–
growing species that rarely lives beyond
3 years of age. However, least chub in
natural systems live longer than
originally thought (some least chub may
live to be 6 years of age) and growth
rates vary among populations (Mills et
al. 2004a, p. 409). Differences in growth
rates may result from a variety of
interacting processes, including food
availability, genetically based traits,
population density, and water
temperatures (Mills et al. 2004a, p. 411).
Least chub are opportunistic feeders,
and their diets reflect availability and
abundance of food items in different
seasons and habitat types (Crist and
Holden 1980, p. 808; Lamarra 1981, p.
5; Workman et al. 1979, p. 23).
Although least chub diets change
throughout the year, they regularly
consume algae (Chlorophyta and
Chrysophyta), midges (Chironomidae),
microcrustaceans, copepods, ostracods,
and diatomaceous material (Sigler and
Sigler 1987, p. 183).
Maintaining hydrologic connections
between springheads and marsh areas is
important in fulfilling the least chub’s
ecological requirements (Crawford 1979,
p. 63; Crist and Holden 1980, p. 804;
Lamarra 1981, p. 10). Least chub follow
thermal patterns for habitat use. In April
and May, they use the flooded, warmer,
vegetated marsh areas at water
temperatures of about 16 °C (60 °F)
(Crawford 1979, pp. 59, 74), but in late
summer and fall they retreat to spring
heads as the water recedes, to
overwinter (Crawford 1979, p. 58). In
the spring, the timing of spawning is a
function of temperature and
photoperiod (Crawford 1979, p. 39).
The least chub is a partial and
intermittent spawner, and spawns
within aquatic vegetation (Crawford
1979, p. 74). Adhesive eggs attach to the
emergent plants that provide the eggs,
larvae, and young with oxygen, food,
and cover (Crist and Holden 1980, p.
808). Females release only a few eggs at
a time, but continue spawning for an
extended period. Total numbers of eggs
produced are an indication of fecundity,
and individual females produce from
300 to 2,700 eggs (Crawford 1979, p. 62).
Fertilized eggs hatch in approximately 2
days at a water temperature of 22 °C (72
°F) (Crawford 1979, p. 74). Although
peak spawning activity occurs in May,
the reproductive season lasts from April
to August, and sometimes longer,
depending on environmental conditions
such as photoperiod and water
temperature (Crawford 1979, pp. 47–48).
This reproductive strategy (i.e.,
repetitive spawning over a period of
many weeks) allows the least chub to
persist in fluctuating environmental
conditions typical of desert habitats
(Crawford 1978, p. 2).
Larval least chub grow larger and
young fry survive better in silt substrate
habitats (Wagner et al. 2006, pp. 1, 4, 7).
The maximum growth rate for least
chub less than 1 year of age occurs at
22.3 °C (72 °F) under captive conditions
(Billman et al. 2006, p. 434). Thermal
preferences demonstrate the importance
of warm rearing habitats in producing
strong year classes and viable
populations (Billman et al. 2006, p.
434).
Distribution
The first documented collection of
least chub is from a ‘‘brook’’ near Salt
Lake City in 1871 (Hickman 1989, p.
16). Between 1871 and 1979, many least
chub occurrences were reported across
the State, ranging from the eastern
portions of the Snake Valley to the
Wasatch Front and from the northern
extent of the Bear River south to the
Beaver River (table 1). Least chub were
very common in tributaries to the
Sevier, Utah, and Great Salt Lakes in the
beginning of the 20th Century (Jordan
1891, p. 30; Jordan and Evermann 1896,
in Hickman 1989, p. 1).
TABLE 1.—SUMMARY OF HISTORIC COLLECTIONS OF LEAST CHUB.
GEOGRAPH AREA
Wasatch Front
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Collected
Location
Northwest Salt Lake City
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Reference
Hickman 1989, pp. 16-17
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TABLE 1.—SUMMARY OF HISTORIC COLLECTIONS OF LEAST CHUB.—Continued
GEOGRAPH AREA
Year
Collected
Location
Reference
Big Cottonwood Creek
1953
Sigler & Miller 1963, pp. 82-83
Davis County (2 miles west of Centerville)
1964
Hickman 1989, pp. 16-17; Bailey et al. 2005, p. 16
Farmington Bay
1965
Hickman 1989, pp. 16-17; Bailey et al. 2005, p. 16
Provo River
1891
Jordan 1891, p. 30
1931 & 1936
Tanner 1936, p. 170
Provo River (at confluence with Utah Lake)
Northern
Bear River
1894
Thompson 2008, p. 1
Southern
Beaver River
1875
Cope & Yarrow 1875, pp. 656-657
Beaver River; Parowan Creek; Clear Creek;
& Little Salt Lake
1942
Hubbs et al. 1942, in Sigler & Miller 1963, p. 82
Sevier Lake
1896
Jordan & Evermann 1896, in Bailey et al. 2005, p.
16
Chimneys Spring; Big Spring; Foote Ranch;
Small Knoll; & Gandy area
1942
Hickman 1989, p. 16-17
Leland Harris Spring Complex & Gandy Salt
Marsh
1970
Hickman 1989, p. 16
Leland Harris Spring Complex; Bishop
Spring Complex (Foote Reservoir & Twin
Spring); & Gandy Spring Complex
1979
Workman et al. 1979, pp. 157-159
Callao, Utah (Bagley Ranch & Redden
Spring)
1979
Workman et al. 1979, pp. 157-159
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Snake Valley
By the 1940s and 1950s, the numbers
of least chub were decreasing (Holden
1974, in Hickman 1989, p. 2). Only 11
known populations existed by 1979
(Workman et al. 1979, pp. 156–158). By
1989, least chub had not been collected
outside of the Snake Valley for the
previous 25 years (Hickman 1989, p. 2).
Three wild least chub populations were
extant in 1995 (60 FR 50518) (Leland
Harris Spring Complex, Gandy Salt
Marsh, Bishop Spring Complex).
The current distribution of the least
chub is highly reduced from its historic
range. The UDWR began surveying for
new populations and monitoring
existing populations Statewide in 1993.
As a result, UDWR found three
previously unknown populations of
least chub: Mona Springs in 1995, Mills
Valley in 1998, and Clear Lake in 2003
(Mock and Miller 2003, p. 3; Hines et al.
2008, pp. 44–45). The Mona Springs site
is in the southeastern portion of the
Great Salt Lake subbasin and occurs on
the eastern border of ancient Lake
Bonneville, near the highly urbanized
Wasatch Front. Clear Lake and Mills
Valley are both in the Sevier subbasin,
in relatively undeveloped sites (Hines et
al. 2008, p. 17). A comparison of survey
results from the 1970s (Workman et al.
1979, pp. 156–158) to surveys from 1993
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to 2007 (Hines et al. 2008, pp. 36–45)
indicates that a majority of the natural
populations extant in 1979 were
extirpated by 2007 (table 2).
Table 2.—Comparison of least chub
collections in 1979 and their updated
status in 2007.
Asterisk (*) denotes populations
discovered after 1979.
Status categories:
• Stable = viable self–sustaining
population
• Functionally extirpated = a limited
number of least chub present but
population is not self sustaining
• Extirpated = least chub no longer
present at that location
• Secure = no immediate threats present
• Not secure = immediate threat(s)
present
1979 Population
Status in 2007
Leland Harris Spring
Complex
Stable – Secure
Gandy Salt Marsh
Stable – Secure
Bishop Springs
Stable – Secure
Mills Valley*
Stable – Not secure
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1979 Population
Status in 2007
Clear Lake Wildlife
Management
Area*
Stable – Not secure
Mona Springs*
Functionally
extirpated
Redden Springs
Extirpated
Bagley Ranch
Complex
Extirpated
Knoll Spring (not
verified)
Extirpated
Cecil Garland Ranch
Extirpated
Tie House
Extirpated
Donner
Extirpated
Cold
Extirpated
Five wild, extant populations of least
chub remain: the Leland Harris Spring
Complex, Gandy Salt Marsh, Bishop
Springs Complex, Mills Valley, and
Clear Lake (Hines et al. 2008, pp. 34–
45). Three of these populations (the
Leland Harris Spring Complex, Gandy
Salt Marsh, and Bishop Spring
Complex) occur in the Snake Valley of
Utah’s west desert and are genetically
similar and very close in proximity to
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each other (Mock and Miller 2003, pp.
17–18). The two remaining extant
populations (Mills Valley and Clear
Lake) are located on the southeastern
border of the native range.
Least chub are still found in small
numbers at the Mona Springs site (Hines
et al. 2008, p. 37). However, because
this small number of least chub does not
compose a viable self–sustaining
population (LCCT 2008a, p. 3), we
consider the least chub population at
Mona Springs functionally extirpated
(see discussion below). The Snake
Valley, Mills Valley, Clear Lake, and
Mona Springs populations are each
genetically distinct (Mock and Miller
2005, p. 276; Mock and Bjerregaard
2007, p. 146). A brief description of the
extant wild and the Mona Springs least
chub populations is found below.
(1) Leland Harris Spring Complex:
R.R. Miller first collected least chub at
this site, located north of the Juab/
Millard County line, in 1970 (Sigler and
Sigler 1987, p. 182). The site consists of
12 to 15 springheads that feed a playa
wetland with habitat fluctuating in size
seasonally. Least chub have had a
persistent presence since monitoring
began by the UDWR in 1993 (Hines et
al. 2008, pp. 41–43). Another spring in
the area, Miller Spring, is part of the
Leland Harris Spring Complex, but
outflows of the two sites are not always
connected.
(2) Gandy Salt Marsh: C.L., L.C., and
E.L. Hubbs first collected least chub at
this site in 1942 (Sigler and Miller 1963,
p. 82). Gandy Salt Marsh is south of the
Millard/Juab County line and the Leland
Harris Spring Complex and consists of
private Utah School and Institutional
Trust Lands Administration (SITLA)
and BLM lands. Measuring
approximately 6.4 kilometers (km) (4
miles (mi)) long (north and south) and
3.2 km (2 mi) wide (east and west), the
complex consists of approximately 52
small springheads or ponds that drain
into a large playa wetland on
approximately 1,295 hectares (ha) (3,200
acres (ac)) (BLM 1992, p. 11). Least chub
is the dominant fish species at the
Gandy Salt Marsh site and comprises a
wild self–sustaining population (Hines
et al. 2008, p. 40). However, the number
of occupied sites within the marsh has
decreased about 50 percent since 1994
(Wilson 2006, p. 8; Hines et al. 2008, p.
41).
(3) Bishop Springs Complex: Least
chub were documented at this site in
1942 (Hickman 1989, p. 18). The
complex is now the largest occupied
least chub site in Snake Valley. Located
south and very near Gandy Salt Marsh,
the site has large springs containing
least chub, including Central Spring and
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Twin Springs (Hines et al. 2008, p. 38).
The least chub population in Bishop
Springs has remained stable and has
demonstrated successful reproduction
and recruitment (Hines et al. 2008, p.
38). The manmade Foote Reservoir does
not contain least chub but contributes
water to the playa marshlands that
provide seasonal least chub foraging,
reproduction, and nursery–type habitat
(Crawford 1979, pp. 62–65).
(4) Mills Valley: UDWR biologists
discovered least chub at multiple
locations at this site in 1998 (Hines et
al. 2008, p. 44). Mills Valley is in the
Sevier River drainage in southeast Juab
County (Hines et al. 2008, p. 17). It
consists of a wetland with numerous
springheads throughout the 200–ha
(495–ac) complex. The least chub were
present during sampling from 2001
through 2006 (Hines et al. 2008, p. 44).
(5) Clear Lake: In 2003, UDWR
biologists found least chub at the Clear
Lake Wildlife Management Area (WMA)
in Millard County (Hines et al. 2008, p.
45). This reserve consists of a shallow
reservoir and diked ponds fed by
springs from adjacent Spring Lake. The
site is managed by UDWR for waterfowl
habitat (Hines et al. 2008, p. 45).
Information about this least chub
population is limited because of its
recent discovery; however, successful
recruitment is occurring (Hines et al.
2008, p. 45).
(6) Mona Springs: The UDWR
biologists discovered this least chub site
in northeast Juab County in 1995 (Mock
and Miller 2003, p. 3). Mona Springs
has provided habitat for a genetically
distinct, naturally occurring population
of least chub. However, the Mona
Springs site is no longer suitable for
least chub because of the presence of
nonnative fish; only four least chub
were collected here in 2008 surveys
(LCCT 2008a, p. 3). Because of the lack
of population viability at this site, we
consider the least chub population at
Mona Springs functionally extirpated.
Translocations
In an attempt to create refuge (an
artificial place of protection for a
species) populations and reestablish
wild populations, 19 introductions of
least chub to new locations rangewide
were attempted by UDWR between 1979
and 2008 (see table 3). Of these, two
sites are currently stable and secure (one
has persisted for 3 years and another for
1 year), seven introductions failed, and
three are not secure. The long–term
success of seven of the transplants is
currently unknown, because they were
initiated in 2008 and monitoring
information is limited. A description of
each of the translocation efforts follows.
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Table 3.—Least chub translocations
attempted from 1979 to 2008.
Status categories:
• Stable = viable self–sustaining
population
• Unstable = a limited number of least
chub present but population is not
self–sustaining
• Extirpated = least chub no longer
present at location
• Secure = no immediate threats present
• Not secure = immediate threat(s)
present
• Unknown = no established sampling
history
Site
Year
Status
Lakepoint Pond
1979
Extirpated
Harley Sanders
Pond
1986
Extirpated
Red Butte Gardens
1987
Extirpated
Walter Springs
1995
Extirpated
Deadman Springs
1996
Extirpated
Antelope Island
2000
Extirpated
Lucin Pond
1989
Unstable –
Not
secure
Garden Creek
Pond
2004
Stable – Not
secure
Atherly Reservoir
2006
Unstable –
Not
secure
Ibis/Pintail Ponds
2007
Extirpated
Red Knolls Pond
2005
Stable –
Secure
Willow Pond
2007
Stable –
Secure
Seven northern
Utah sites
2008
Unknown
(1) Lakepoint Pond, Tooele County: In
1979, 200 least chub from the Leland
Harris Spring Complex were released
into Lakepoint Pond located
approximately 32 km (20 mi) southwest
of Salt Lake City, 1.6 km (1 mi) from the
shore of the Great Salt Lake. This site
was eliminated by floods in 1983 and
1984 (Hickman 1989, p. 4).
(2) Harley Sanders Pond, Box Elder
County: In 1986, UDWR released least
chub into Harley Sanders Pond and
spring. No least chub were found during
sampling in 1988 (Hickman 1989, p. 4).
(3) Red Butte Gardens, Salt Lake
County: In 1987, least chub were
introduced into the stream and pond at
the Utah State Arboretum (Red Butte
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Gardens) near Fort Douglas in Salt Lake
City (Hickman 1989, p. 5). Attempts to
relocate least chub in 1988 were
unsuccessful (Hickman 1989, p. 5), so
we consider it extirpated and
unsuccessful.
(4, 5) Walter/Deadman Springs,
Tooele County: Least chub were
introduced in 1995 and 1996 to these
springs; however, they have been
replaced by western mosquitofish
(Gambusia affinis) (Wilson and Whiting
2002, p. 4; Wilson and Mills 2004, pp.
4–5). Therefore, we consider these sites
to be extirpated and unsuccessful.
(6) Antelope Island, Davis County: In
December 2000, UDWR introduced least
chub to a human–made spring–fed pond
on Antelope Island. Mosquitofish have
replaced least chub at this site
(Thompson 2005, pp. 5–6). Therefore,
we consider this site to be extirpated
and unsuccessful.
(7) Lucin Pond, Box Elder County: In
1989, 42 least chub were transplanted
into this site. Lucin Pond is a human–
made pond built in the early 1900s. This
least chub population is currently
considered unstable and not secure
because mosquitofish are present and
the water supply to the pond is
unreliable (Thompson 2005, pp. 1–4;
Hines et al. 2008, pp. 47–49).
(8) Garden Creek Pond, Davis County:
In 2004, 947 least chub were introduced
to this pond on Antelope Island in the
Great Salt Lake. It is a 0.04 ha (0.1 ac)
pond that was dredged by the Utah
Department of Parks and Recreation and
is fed by a perennial stream (stream
with continuous flow throughout the
year). The site was considered a genetic
refuge for the functionally extirpated
Mona Springs population. Reproduction
and recruitment have been occurring;
however, the site is threatened by a loss
of habitat due to siltation (Thompson
2005, pp. 6–7; Hines et al. 2008, p. 46;
Thompson 2008, p. 3; LCCT 2008a, pp.
3–4).
(9) Atherly Reservoir, Tooele County:
This site is on Faust Creek in Rush
Valley, and is part of the 283–ha (700–
ac) James Walter Fitzgerald WMA.
Approximately 13,000 least chub from
the Mills Valley population were
introduced in 2006 (Hines et al. 2008, p.
50). The UDWR monitoring in 2008
detected only eight least chub (LCCT
2008a, p. 3). Therefore, we do not
consider this introduction to be
successful at this time.
(10) Ibis/Pintail Ponds, Tooele
County: In 2007, least chub from Leland
Harris Spring Complex were introduced
into Ibis and Pintail Ponds on the Fish
Springs National Wildlife Refuge (Hines
et al. 2008, p. 50). This introduction was
unsuccessful, and the site currently
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does not contain a least chub
population. The UDWR is planning to
release least chub again in the future
after mosquitofish control issues are
addressed (LCCT 2008a, p. 3).
(11) Red Knolls Pond, Box Elder
County: In 2005, 250 least chub from
Bishop Springs were introduced to Red
Knolls Pond (Hines et al. 2008, p. 50),
located in the western portion of Box
Elder County on BLM land. Successful
recruitment was observed in 2005, 2006,
and 2007, indicating that reproduction
has been occurring (Hines et al. 2008, p.
50; Thompson 2008, p. 4). This site is
currently secure and represents a
genetic refuge for the Bishop Springs
Complex population.
(12) Willow Pond, Box Elder County:
On August 22, 2007, 340 least chub
from the Clear Lake population were
released into this habitat (Hines et al.
2008, p. 50), located in the northwest
portion of Box Elder County. In 2008,
least chub were present and recruitment
to the population was apparent (LCCT
2008a, p. 4). This site is currently secure
and represents a genetic refuge for the
Clear Lake population.
(13) The UDWR introduced least chub
into seven additional sites in Cache and
Box Elder Counties in 2008 (LCCT
2008a, p. 4). This effort was conducted
to establish new refuge populations by
stocking State–hatchery–produced least
chub into suitable habitat. Success of
these introductions cannot be
determined for several years; however,
the probability of success for some of
these introductions may be low because
of the possibility of winter kill and the
presence of nonnative species.
In summary, we believe that
translocated least chub populations can
contribute to the long–term
conservation of the species by providing
a refuge (e.g., hatcheries or other
managed systems) for the preservation
of a population’s genetic diversity. In
addition, translocation to a refugium (a
native habitat that has escaped
ecological changes occurring elsewhere
and so provides a suitable habitat for a
species) contributes to long–term
conservation of least chub by providing
conditions necessary to maintain a
viable self–sustaining population.
However, to date, translocated least
chub populations have had relatively
poor success because of problems with
competing nonnative fishes, inadequate
water supply, or for unknown reasons
(i.e., least chub were stocked into a
particular habitat but could not be
relocated during subsequent
monitoring). While two populations
have indications of successful
recruitment and are secure from
immediate threats, it is too early to
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determine whether these populations
will contribute to the long–term
conservation of least chub. Monitoring
of translocated populations will be
essential to address the uncertainty that
exists about the success of these actions.
Due to the uncertainty of the long–term
status of translocated least chub
populations, they are not considered
further in this review.
Hatchery Broodstock
The Wahweap Warmwater Fish
Hatchery in Big Water, Utah, and the
Fisheries Experiment Station in Logan,
Utah, each manage least chub
broodstock that were sourced from Mills
Valley and Mona Springs (Hines et al.
2008, p. 27). These hatcheries help
preserve the genetic diversity of source
populations of least chub and provide
stock for introduction and
reintroduction efforts.
Summary of Information Pertaining to
the Five Factors
Section 4 of the Act (16 U.S.C. 1533),
and implementing regulations (50 CFR
424), set forth procedures for adding
species to the Federal Lists of
Endangered and Threatened Wildlife
and Plants. Under section 4(a)(1) of the
Act, a species may be determined to be
endangered or threatened based on any
of the following five factors: (A) The
present or threatened destruction,
modification, or curtailment of its
habitat or range; (B) overutilization for
commercial, recreational, scientific, or
educational purposes; (C) disease or
predation; (D) the inadequacy of
existing regulatory mechanisms; or (E)
other natural or manmade factors
affecting its continued existence. In
making this finding, information
pertaining to the least chub in relation
to the five factors provided in section
4(a)(1) of the Act is discussed below.
Factor A. The Present or Threatened
Destruction, Modification, or
Curtailment of the Species’ Habitat or
Range.
The following potential threats that
may affect the habitat or range of least
chub are discussed in this section,
including: (1) Livestock grazing; (2) oil
and gas leasing and exploration; (3)
mining; (4) urban and suburban
development; (5) water withdrawal and
diversion; and (6) drought.
(1) Livestock Grazing
Grazing animals can impact aquatic
habitats in multiple ways. Livestock
seek springs for food and water, both of
which are limited in desert habitats;
therefore, they spend a disproportionate
amount of time in these areas (Stevens
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and Meretsky 2008, p. 29). As they
spend time at springs, livestock eat and
trample plants, compact local soils, and
collapse banks of springs (Stevens and
Meretsky 2008, p. 29). Input of organic
wastes increases nutrient
concentrations, and some nutrients (i.e.,
nitrogen compounds) can become toxic
to fish (Taylor et al. 1989, in Stevens
and Meretsky 2008, p. 29). Domestic
animals can also be trapped in soft
spring deposits, die and decompose,
and pollute the water. All of these
effects can result in the loss or decline
of native aquatic fauna (Stevens and
Meretsky 2008, pp. 29–30).
As explained below, historic livestock
grazing impacted four of the five
remaining wild least chub sites, and
current livestock grazing practices
continue to impact these sites. The
UDWR monitors these sites and is
working on minimizing or removing
livestock grazing threats (Hines et al.
2008, pp. 22–23). Livestock grazing
impacts occur at Mills Valley (Wilson
and Whiting 2002, pp. 2–3; Bailey 2006,
p. 30; Hines et al. 2008, p. 43), Gandy
Salt Marsh (Hines et al. 2008, p. 39;
LCCT 2008b, p. 2), Miller Spring/Leland
Harris Spring Complex (Bailey 2006, p.
11; Hines et al. 2008, pp. 41–42), and
Bishop Springs/Foote Reservoir/Twin
Springs (Wheeler and Fridell 2005, p.
5). The Clear Lake site is protected from
livestock grazing because it is a WMA
managed by the State of Utah (Hines et
al. 2008, p. 45).
Fencing at Gandy Salt Marsh and
Miller Spring/Leland Harris Spring
Complex excludes cattle from
springhead areas (Hines et al. 2008, pp.
39, 41, 43), but livestock damage still
occurs at these sites during periods of
unmanaged overgrazing or when fences
are not maintained (Hines et al. 2008, p.
39; LCCT 2008b, p. 2). For example, in
July 2008, livestock damage was
reported to be extensive and fencing
trapped cattle inside the northern area
of Gandy Salt Marsh (LCCT 2008b, p. 2).
Impacts from livestock grazing
include bank erosion and sedimentation
to springheads (LCCT 2008b, p. 5).
Miller Spring (at the Leland Harris
Spring Complex) was unsuitable for
least chub due to sedimentation and
trampling associated with livestock use,
poor water quality, and the presence of
rainbow trout (Hogrefe 2001, p. 7).
Extensive efforts by UDWR in 1999 and
2000 to restore and fence the spring and
remove nonnatives significantly
improved the habitat (Hogrefe 2001, pp.
7, 20); however, the response of least
chub to improvements at Miller Spring
has not been determined. Most of the
other 12 to 15 springs in the Leland
Harris Spring Complex have some
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ungulate damage and bank disturbance
(Hines et al. 2008, p. 42). A rotational
grazing plan has been developed with
the landowner and UDWR on 75 ha (188
ac) of the Leland Harris site to improve
habitat conditions, but damage to
springs and riparian vegetation
continues to impact least chub habitat
(Hines et al. 2008, p. 42).
Twin Springs, at the Bishop Spring
complex, is partially protected from
livestock by fences, but the larger spring
complex, Twin Springs South, is not
protected from grazing or wild horse
watering access. Twin Springs South
has severely impacted banks resulting in
shallower water, increased surface area,
and sedimentation of spring heads
(Wheeler et al. 2004, p. 5). On the State–
owned WMA portion of the Mills Valley
site, grazing is allowed in return for
access across private land. The private
portion of Mills Valley is overgrazed
and damage to water body banks and
riparian vegetation has been reported as
moderate to severe (UDWR 2006, pp.
27–28). The BLM has built fencing
around two Gandy Salt Marsh
springheads, Pilot Springs and Red
Knolls Pond, to protect least chub
transplant locations (Hines et al. 2008,
p. 24).
In summary, our analysis indicates
that, although efforts to control and
minimize damage have been
implemented and are ongoing, livestock
grazing impacts some habitat at most
wild least chub sites. Grazing damage is
not always severe where it occurs, and
livestock are effectively excluded from
portions of occupied habitat. However,
extensive livestock grazing–related
damage has occurred in the last couple
of years in some instances, and livestock
grazing on private lands where least
chub occur is still partially unregulated.
Therefore, we conclude that current
levels of livestock grazing are likely to
significantly threaten least chub
populations at Leland Harris Spring
Complex, Gandy Salt Marsh, Bishop
Springs Complex, and Mills Valley, now
and in the foreseeable future.
(2) Oil and Gas Leasing and Exploration
Oil and gas leasing and exploration
can have direct and indirect impacts on
springs, marshes, and riparian habitats.
Vehicles, including drilling rigs and
recording trucks, can crush vegetation,
compact soils, and introduce exotic
plant species (BLM 2008, pp. 4–9 to 4–
20). Roads and well pads can affect local
drainages and surface hydrology, and
increase erosion and sedimentation
(Matherne 2006, p. 35). Accidental
spills (Etkin 2009, pp. 36–42, 56) can
result in the release of hydrocarbon
products into ground and surface waters
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35403
(Stalfort 1998, section 1).
Accumulations of contaminants in
floodplains can result in lethal or
sublethal impacts to endemic sensitive
aquatic species (Stalfort 1998, section 4;
Fleeger et al. 2003, p. 207).
All of the naturally occurring, extant
least chub populations occur within the
Fillmore BLM area. The majority of
BLM land in the Fillmore Field Office
is open to oil and gas leasing (BLM
2009a, p. 11). Oil and gas leases have
been sold within the watershed areas of
most of the naturally occurring least
chub populations, but the closest active
well to a least chub population is
currently 9.7 km (6 mi) away (Megown
2009a, entire). The Gandy Salt Marsh
population area is closed to leasing by
BLM in accordance with the Fillmore
Resource Management Plan (RMP)
because of the occurrence of least chub
habitat. This RMP will be updated in
approximately 10 to 15 years. Any
change to the management direction
would be reviewed at this time and
subject to public comment (BLM 2009a,
p. 54). Seismic surveys were conducted
on parcels adjacent to the Mills Valley
population, and BLM anticipates that a
Notice of Staking or Application for
Permit to Drill may be filed by the lessee
in 2010 (Mansfield 2009, p. 1).
Based on past drilling history, the
BLM’s Fillmore Field Office determined
that recoverable oil and gas is likely to
be of low availability within the range
of the least chub. They further estimated
that exploratory wells will be drilled at
the rate of about one well every year for
the foreseeable future (BLM 2009a, p.
52). Leases near least chub habitat will
not be offered for sale until the Fillmore
BLM RMP is revised; the RMP revision
is not yet scheduled (Naeve 2009a–c,
entire).
Oil and gas leases in the BLM
Fillmore Field Office will include lease
notices with information on sensitive
species and conservation agreement
species where appropriate (BLM 2009a,
pp. 14, 98–99). These lease notices
include measures to coordinate with
UDWR to minimize the risk of spreading
aquatic exotic species; avoid surface
pumping for water; avoid surface
disturbances within 100–year
floodplains; avoid changes to ground
and surface hydrology; and avoid direct
disturbances to special status species
(BLM 2009a, pp. 98–99). The extent of
implementation of each lease notice,
and the success of the lease notices, will
not be known until development occurs.
However, the lease notices in
combination with the low energy
development potential should ensure
that oil and gas development is not a
significant threat to the species in the
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foreseeable future. Recoverable oil and
gas across the entire Fillmore Field
Office area is expected to be low, with
a rate of one exploratory well drilled
annually, and the nearest active well is
9.7 km (6 mi) from an extant least chub
population. We conclude that oil and
gas development are not anticipated to
occur at a level that will threaten least
chub.
srobinson on DSKHWCL6B1PROD with PROPOSALS
(3) Mining
Mills Valley contains a bog area with
a peat and humus resource (Olsen 2004,
p. 6). Peat mining has the potential to
alter the hydrology and habitat
complexity of Mills Valley, making it
unsuitable for least chub (Bailey et al.
2005, p. 31). An illegal peat removal
activity occurred on private lands in the
Mills Valley wetlands in 2003 (Wilson
2009a, pers. comm.). The illegal activity
was less than 0.2 ha (0.5 ac) in size, and
impacts to associated wetlands were
restored (Wilson 2009a, pers. comm.). In
2003, a Mills Valley landowner received
a permit from the Utah Division of Oil,
Gas, and Mining to conduct peat mining
on their private land. Although one test
hole was dug, no further peat mining
occurred in this location. This peat
mining permit is now inactive and
noncompliant with State regulations
requiring payment of mining and bond
fees (Wilson 2009a, pers. comm.). Past
peat mining activities have been
unsuccessful in Mills Valley, and we are
unaware of any future private or
commercial peat mining proposals.
In summary, our analysis found one
illegal peat removal activity and one
abandoned attempt at legal peat removal
in the Mills Valley least chub
population area. We are unaware of any
additional private or commercial peat
operation proposals in Mills Valley. We
conclude that peat mining is not
anticipated to occur at a level that will
threaten least chub.
(4) Urban and Suburban Development
Urban and suburban development
affect least chub habitats through: (1)
Changes to hydrology and sediment
regimes; (2) inputs of pollution from
human activities (contaminants,
fertilizers, and pesticides); (3)
introductions of nonnative plants and
animals; and (4) alterations of
springheads, stream banks, floodplains,
and wetland habitats by increased
diversions of surface flows and
connected groundwater (Dunne and
Leopold 1978, pp. 693–702).
The least chub was originally
common throughout the Bonneville
Basin in a variety of habitat types (Sigler
and Miller 1963, p. 82). In many
urbanized and agricultural areas,
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residential development and water
development projects have effectively
eliminated historical habitats and
potential reintroduction sites for least
chub (Keleher and Barker 2004, p. 4;
Thompson 2005, p. 9). Development
and urban encroachment have either
functionally or completely eliminated
most springs, streams, and wetlands
along the Wasatch Front (Keleher and
Barker 2004, p. 2).
The Mona Springs site, as well as
potential reintroduction sites (Keleher
and Barker 2004, p. 4; Thompson 2005,
p. 9) on the Wasatch Front, are
vulnerable to rapid population growth.
The human population in the Mona
Springs area has increased 64.9 percent
from 2000 to mid 2008 (City–Data 2009,
p. 1) and a housing development has
expanded to within 1 km (0.6 mi) of the
Mona Springs least chub site (Megown
2009b, entire). The URMCC, which is
responsible for mitigating impacts
caused by Federal reclamation projects
to fish, wildlife, and related recreation
resources in Utah, has purchased and
protected much of the Mona Springs
habitat areas for conserving least chub
and spotted frog populations (see Factor
D). However, indirect effects of urban
development such as pollution from
urban stormwater runoff and changes to
hydrologic sediment regimes (e.g.,
sedimentation from adjacent
construction activities) could negatively
impact the aquatic habitats at Mona
Springs. Even if mosquitofish and other
predacious nonnative fish (the primary
threat at this site) can be controlled in
the future, we believe urban–
development–related effects could rise
to a level that may preclude
reestablishment of a viable least chub
population at Mona Springs.
Despite the effects of urban and
suburban development on historic
populations of least chub, we have no
information indicating this is a threat to
the five remaining extant least chub
populations. These least chub
populations occur in relatively remote
portions of Utah with minimal human
populations. No information is available
indicating the level of human
occupation near these sites. However,
the population centers nearest to extant
least chub populations are more than 16
km (10 mi) away and have populations
of less than 3,000 persons (Utah
Governor’s Office of Planning and
Budget 2009, entire).
To summarize, development along the
eastern portion of the least chub historic
range has contributed to the elimination
of most of the historic populations of
least chub. The Mona Springs site is
currently the only site in this geographic
area that still contains least chub, but
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the population is functionally
extirpated. We have no information
suggesting that future urban or suburban
development will occur at a level that
will threaten least chub.
(5) Water Withdrawal and Diversion
Hydrologic alterations, including
water withdrawal and diversion, affect a
variety of abiotic and biotic factors that
regulate least chub population size and
persistence. Abiotic factors include
physical and chemical characteristics of
the environment, such as water levels
and temperature, while biotic factors
include interactions with other
individuals or other species (Deacon
2007, pp. 1–2). Water withdrawal
directly reduces available habitat,
impacting water depth, water surface
area, and flows from springheads (Alley
et al. 1999, p. 43). As available habitat
decreases, the characteristics and value
of the remaining habitat changes.
Reductions in water availability to least
chub habitat reduce the quantity and
quality of the remaining habitat (Deacon
2007, p. 1).
Water withdrawal and diversion
reduces the size of ponds, springs, and
other water features that support least
chub (Alley et al. 1999, p. 43).
Assuming that the habitat remains at
carrying capacity for the species or, in
other words, assuming all population
processes (birth rate, death rate, etc.)
remain unchanged, smaller habitats
support fewer individuals by offering
fewer resources for the population
(Deacon 2007, p. 1).
Because least chub live in patchily
distributed desert aquatic systems,
reduction in habitat size also affects the
quality of the habitat. Reduced water
depth may isolate areas that would be
hydrologically connected at higher
water levels. Within least chub habitat,
springheads offer stable environmental
conditions, such as temperature and
oxygen levels, for refugia and
overwintering, but offer little food or
vegetation (Deacon 2007, p. 2). In
contrast, marsh areas offer vegetation for
spawning and feeding, but exhibit wide
fluctuations in environmental
conditions (Crawford 1979, p. 63; Crist
and Holden 1980, p. 804). Maintaining
hydrologic connections between
springheads and marsh areas is
important because least chub migrate
between these areas to access the full
range of their ecological requirements
(Crawford 1979, p. 63; Crist and Holden
1980, p. 804; Lamarra 1981, p. 10).
Although we have not directly
observed the effects of flow reductions
on wild least chub populations, we
believe that flow reductions will reduce
the hydrology that supports wetland
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and wetland/upland transition zones
which, in turn, provide vegetation
needed for the least chub reproductive
cycle (Crawford 1979, p. 38; Lamarra
1981, p. 10). Alterations of natural flow
processes also could alter sediment
transport processes that prevent
vegetation encroachment into sensitive
spring areas (60 FR 50520).
Reductions in water may alter
chemical and physical properties of
aquatic habitats. As water quantity
decreases, temperatures may rise
(especially in desert ecosystems with
little shade cover), dissolved oxygen
may decrease, and the concentration of
pollutants may increase (Alley et al.
1999, p. 41; Deacon 2007, p. 1). These
modified habitat conditions are likely to
significantly impact least chub life
history processes, possibly beyond the
state at which the species can survive.
The maximum growth rate for least
chub less than 1 year of age would occur
at 22.3 °C (72.1 °F). Temperatures above
or below this have the potential to
negatively impact growth and affect
survival rates (Billman et al. 2006, p.
438).
Reduced habitat quality and quantity
may cause niche overlaps with other
fish species, increasing hybrid
introgression, interspecific competition,
and predation (Deacon 2007, p. 2) (see
Factor C. Predation; Factor E.
Hybridization). Reduction in flow of
springs reduces opportunities for habitat
niche partitioning; therefore, fewer
species are able to coexist. The effect is
especially problematic with respect to
introduced species. Native species may
be able to coexist with introduced
species in relatively large habitats (see
Factor C. Predation), but become
increasingly vulnerable to extirpation as
habitat size diminishes (Deacon 2007, p.
2).
Habitat reduction may affect the
species by altering individual success.
Fish and other aquatic species tend to
adjust their maximum size to the
amount of habitat available, so reduced
habitat may reduce the growth capacity
of least chub (Smith 1981, in Deacon
2007, p. 2). Reproductive output
decreases exponentially as fish size
decreases (Deacon 2007, p. 2).
Therefore, reduction of habitat volume
in isolated desert springs and streams
reduces reproductive output (Deacon
2007, p. 2). Longevity also may be
reduced resulting in fewer reproductive
seasons (Deacon 2007, p. 2).
Current Groundwater Pumping
The Utah State Engineer (USE),
through the Utah Division of Water
Rights (UDWRi), is responsible for the
administration of water rights, including
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the appropriation, distribution, and
management of the State’s surface and
groundwater. This office has broad
discretionary powers to implement the
duties required by the office. The USE’s
Office was created in 1897, and the
State Engineer is the chief water rights
administrative officer. For groundwater
management, Utah is divided into
groundwater areas, and policy is
determined by area (BLM 2009b, entire).
A joint report by the U.S. Geological
Survey (USGS) and several State of Utah
agencies provided a description of
groundwater conditions in the State of
Utah for 2008 (Burden 2009, entire).
Each of the locations occupied by least
chub had a corresponding summary by
valley or hydrographic area for: the
number of wells constructed in 2008;
the total estimated groundwater
withdrawn in the area for 2008; the total
estimated groundwater withdrawn for
each year for the previous 10 years; and
groundwater level monitoring results
from several monitoring wells for
varying periods of record (~20 to 75
years). For all valleys and hydrographic
areas, the predominant (greater than 79
percent) use of withdrawn groundwater
was for irrigation with remaining uses
including industrial, public supply,
domestic, and stock (Burden 2009, pp.
5, 89).
The Juab Valley, where the Mona
Springs least chub site is located, had a
total of two new wells, and 26,000 acre–
feet per year (afy) withdrawn for 2008
(Burden 2009, pp. 3–5). This is more
than double the amount withdrawn in
1998 (12,000 afy) and is an overall
increase from the 1998–2007 average
(22,000 afy) (Burden 2009, p. 6). All
supplies of surface and groundwater are
fully appropriated; however, new wells
could be developed with existing
groundwater rights (UDWRi 2009d, pp.
1–2).
Although the Mills Valley population
site did not have a corresponding
pumping area in the report, the Central
Sevier Valley summary represents
pumping activity in the river valley
upstream of this population and may be
indicative of the potential for
groundwater withdrawal effects. The
Central Sevier Valley had a total of 13
new wells, and 24,000 afy withdrawn in
2008 (Burden 2009, pp. 3–5). This is
4,000 afy more than the amount
withdrawn in 1998 (20,000 afy) and is
an 8,000–afy increase from the 1998–
2007 average (16,000 afy) (Burden 2009,
p. 6). Since 1997, the corresponding part
of the Sevier River Basin was closed to
all new appropriations of groundwater.
However, new groundwater
development can occur under existing
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groundwater rights (UDWRi 2009d, pp.
3–4).
The Clear Lake least chub site is
located within the Sevier Desert
groundwater pumping basin, which had
11 new wells with 44,000 afy
withdrawn in 2008 (Burden 2009, pp.
3–5). This is 32,000 afy more than the
amount of water withdrawn in 1998
(12,000 afy) and is a 20,000–afy increase
from the 1998–2007 average (24,000 afy)
(Burden 2009, p. 6). Since 1997, this
part of the Sevier River Basin was
closed to all new appropriations of
groundwater except for domestic filings
not exceeding 1.0 acre–foot and for
filings reviewed on an individual basis
in limited areas of the basin (UDWRi
2009d, pp. 5–6).
The Snake Valley summary, which
corresponds to the pumping activity in
the vicinity of Leland Harris Spring
Complex, Gandy Salt Marsh, and Bishop
Spring Complex did not report the
number of new wells, but did specify
19,800 and 20,200 afy withdrawn for
2007 and 2008, respectively, in Utah
(Burden 2009, p. 89). Additional
information on groundwater pumping
over the last decade was not provided.
State of Nevada Division of Water
Resources reported that 11,000 afy of
groundwater was pumped from the
Nevada portion of Snake Valley in 2009
(NDWR 2009, entire). Groundwater is
currently open to appropriation in
Snake Valley in Utah (UDWRi 2009d,
pp. 7–9) and Nevada (NDWR 2009,
entire).
The previously discussed increases in
groundwater pumping have occurred at
the same time that a declining trend in
groundwater level was observed at wells
monitored in or very near basins with
least chub populations (Burden 2009,
pp. 41–57, 89, 96). Groundwater
monitoring shows that water levels
generally rose in the early to mid 1980s,
likely as a result of greater–than–average
precipitation. However, groundwater
levels generally declined from the mid–
to–late 1980s to the present. Although
drought conditions were present in the
eastern Great Basin (areas with extant
least chub populations) during this time
(See Factor A. Drought), localized
annual precipitation levels were either
average to slightly above average (Mona
Springs and Mills Valley least chub
sites) or were generally increasing, if
below average (Clear Lake and Snake
Valley least chub sites), during this
same timeframe (Burden 2009, pp. 41–
57, 89, 96).
For the four basins discussed above,
a more specific analysis of groundwater
level fluctuations over the last decade
(1998–2009) provides some indication
of the scope of change. Groundwater
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levels from six monitoring wells in Juab
Valley (where the Mona Springs least
chub site is located) declined an average
of 6.1 meters (m) (20 feet (ft)) with
declines ranging from 0.6 to 10.1 m (2
to 33 ft) (Burden 2009, pp. 41–45). As
stated above, groundwater monitoring in
Central Sevier Valley basin represents
pumping activity and groundwater
levels in the river valley upstream of the
Mills Valley least chub population and
may be indicative of the potential for
groundwater withdrawal effects.
Groundwater levels in 10 monitoring
wells in this area declined an average of
0.9 m (3 ft) with declines ranging from
0 to 1.5 m (0 to 5 ft). Data from 15
monitoring wells in the Sevier Desert
groundwater pumping basin (where the
Clear Lake least chub site is located)
indicated that groundwater levels
declined an average of 2.4 m (8 ft) with
declines ranging from 0.3 to 5.5 m (1 to
18 ft), and groundwater monitoring
levels in the Snake Valley (in the
vicinity of Leland Harris Spring
Complex, Gandy Salt Marsh, and Bishop
Spring Complex) declined 1.2 m (4 ft)
with declines ranging from 0.3 to 3 m
(1 to 10 ft) (Burden 2009, pp. 46–52, 89–
96).
We have limited information linking
groundwater pumping to decreases in
flow at sites where least chub
previously existed. Agricultural
pumping, combined with drought, has
affected several springs in Snake Valley.
These include Knoll Spring near the
town of Eskdale and springs on private
properties in the town of Callao (Sabey
2008, p. 2). These sites were all
historically documented locations of
least chub that no longer harbor the
species (Hickman 1989, pp. 16–17;
Garland 2007, pers. comm.).
Pumping for agricultural purposes,
combined with the effects of drought,
has impacted flow in a number of
springs in Snake Valley. Although no
least chub historically occurred at
Needle Point Spring, the BLM has
detailed monitoring information linking
nearby groundwater pumping and its
effect on the spring’s flow. In 2001, the
water level at Needle Point Spring in
Southern Snake Valley dropped to
levels not seen in 40 years (Summers
2008, pp. 1–2). This spring has a long
history of existence, identified as early
as 1939 by the Civilian Conservation
Corps, when springflow was measured
at 6 gallons per minute (Summers 2008,
p. 1). For the past several decades, the
spring was developed and used for
watering livestock and wild horses
(Summers 2008, p. 1). The 2001 decline
in groundwater level at Needle Point
Spring was likely the result of, and
coincides with, increased irrigation in
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Hamlin Valley approximately 3.2 km (2
mi) west, and not a result of the lowered
precipitation (Summers 2008, p. 3).
Although the causal effect of
groundwater pumping is unknown in
the following observations, UDWR has
documented decreases in habitat at two
least chub sites. They recently reported
decreases in least chub habitat from
springs drying and decreasing in size at
the Clear Lake least chub site (LCCT
2008b, p. 2). The UDWR found that
annual drying of some ponds with least
chub is becoming a consistent trend
resulting in declining habitat quality,
and is therefore limiting the distribution
of least chub at Clear Lake. Average
water depth among affected ponds
decreased from 0.5 m (1.6 ft) in 2006 to
0.2 m (0.7 ft) in 2008 (LCCT 2008b, p.
2). At the Gandy Salt Marsh site, least
chub populations have declined by
more than 50 percent (from 1993 to
2006) as a result of a reduction in
available habitats due to the drying of
springs throughout the complex (Wilson
2006, p. 8).
As described above, current
groundwater pumping levels have
increased in the last 10 years and in
some locations have more than doubled.
Groundwater levels have decreased
during this same time period while
precipitation levels were average or
generally increasing if below average.
Negative impacts to least chub habitat
were documented at the same time this
scenario was occurring. In addition, all
basins where least chub occur are
currently open to additional
groundwater pumping. Therefore, we
conclude that current levels of
groundwater pumping are likely to
significantly threaten all least chub
populations now and in the foreseeable
future.
Snake Valley has harbored the most
secure least chub populations over the
past 50 years (Hickman 1989, p. 2;
Hines et al. 2008, pp. 34–45). As
detailed in the following sections of this
document, proposed water development
projects intend to transport water from
the underlying aquifers in the vicinity of
Snake Valley. Projects include a
Southern Nevada Water Authority
(SNWA) Groundwater Development
(GWD) Project, appropriation of
groundwater by the Central Iron County
Water Conservancy District and Beaver
County, Utah, and an increase of water
development by the Confederated Tribes
of the Goshute Reservation. These water
withdrawals threaten to change the
underlying hydrology of the area and
may modify least chub habitat and
impact the extant populations in the
Snake Valley in the foreseeable future
(see below for more information).
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Southern Nevada Water Authority
Proposed Groundwater Development
Project
One of the most significant threats to
extant least chub populations may be
proposed groundwater withdrawals
from the Snake Valley aquifer. Several
applications for groundwater
withdrawal from the Snake Valley
aquifer are pending (SNWA 2008, p. 1–
6), and 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 (SNWA 2008, p. 1–3). The
SNWA GWD Project includes
construction and operation of
groundwater production wells, water
conveyance facilities, and power
facilities (SNWA 2008, p. 1–3). The
proposed production wells and facilities
would be located predominately on
public lands managed by BLM (SNWA
2008, p. 1–3).
As proposed, the SNWA GWD Project
would convey up to 170,000 afy of
groundwater from hydrographic basins
in Clark, Lincoln, and White Pine
Counties, Nevada, to SNWA member
agencies and the Lincoln County Water
Conservancy District (SNWA 2008, p. 1–
1). Although all SNWA facilities are
planned for development in Nevada,
associated pumping from the Spring
Valley and Snake Valley hydrographic
basins (SNWA 2008, pp. 1–4, Figures 1–
2) is expected to affect Utah
groundwater resources and
consequently habitats of the least chub
(Welch et al. 2007, p. 82).
The SNWA would receive all
groundwater conveyed from the Snake
Valley (approximately 50,679 afy) and
Spring Valley (approximately 68,000
afy) Basins (SNWA 2008, p. 1–6, Table
1–1). The groundwater that SNWA
intends to convey would be from
existing and future permitted water
rights (SNWA 2008, p. 1–6, Table 1–1).
If all permits are granted, SNWA
intends to start pumping operations for
Spring Valley in 2028 and Snake Valley
in 2050 (BLM 2009, p. 2–12). As
substantiated below, the SNWA GWD
project is likely to significantly threaten
least chub populations in the
foreseeable future.
The Service has been concerned about
impacts from this proposed large–scale
water withdrawal for many years. In
1990, the Service and other Department
of the Interior (DOI) agencies (BLM,
National Park Service, and Bureau of
Indian Affairs) protested water rights
applications in Spring and Snake
Valley, based in part on potential
impacts to water–dependent natural
resources (Plenert 1990, p. 1; Nevada
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State Engineer (NSE) 2007, p. 11). In
2006, DOI agencies reached a stipulated
agreement with SNWA for the Spring
Valley water rights applications,
withdrew their protests, and did not
participate in the NSE’s hearing (NSE
2007, p. 11). For the Spring Valley
portion of the project, the Stipulated
Agreement established a process for
developing and implementing
hydrological and biological monitoring,
management, and mitigation for
biological impacts (NSE 2007, p. 11).
To better understand the potential
effects of the proposed large–scale
groundwater pumping, the NSE issued
an October 28, 2008 order (Interim
Order No. 2 and Scheduling Order) in
which the applicant (SNWA) was
required to provide a groundwater
model that simulates groundwater
pumping and potential impacts from
pumping in the amount of 10,000,
25,000, and 50,000 afy for the
timeframes of 10, 25, 50, 100, and 200
years. The NSE hearings on these
applications were scheduled to begin on
September 28, 2009. These hearings
were postponed based on a pending
agreement between the States of Nevada
and Utah as described below.
According to the Lincoln County
Conservation, Recreation, and
Development Act (LCCRDA) of 2004
(LCCRDA 2004, entire), the States must
reach an agreement on the division of
Snake Valley groundwater prior to any
transbasin groundwater diversions. Utah
and Nevada have reached a draft
agreement that is still under discussion
and not yet finalized (Kikuchi and
Conrad 2009, p. 3; Styler and Biaggi
2009, entire). As drafted, the agreement
preserves and protects existing water
rights, defines the available
groundwater supply in Snake Valley as
132,000 afy, provides 41,000 afy of
unallocated water to Utah and Nevada,
and monitors withdrawals to identify
and avoid adverse impacts (Kikuchi and
Conrad 2009, p. 2).
To assist in developing this
agreement, the LCCRDA required a
study of groundwater quantity, quality,
and flow characteristics in the carbonate
and alluvial aquifers of White Pine
County, Nevada; groundwater basins
located in White Pine or Lincoln
Counties, Nevada; and adjacent areas of
east–central Nevada and western Utah
(Welch et al. 2007, p. iii). The USGS, the
Desert Research Institute, and the State
of Utah conducted this Basin and Range
Carbonate Aquifer System (BARCAS)
study. The USGS released a final report
of the BARCAS study on February 22,
2008 (Welch et al. 2007, entire).
The BARCAS study included a water–
resources assessment of the geologic
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framework and hydrologic processes
influencing the quantity and quality of
groundwater resources. The USGS
determined that groundwater systems
underlying many of the valleys in
eastern Nevada and western Utah are
not isolated, but rather contribute to or
receive flow from adjoining basins
(Welch et al. 2007, pp. 4-5). They also
determined that some large-volume
springs cannot be supported entirely by
the local recharge from the adjacent
mountains; these springs depend on
water from potentially hundreds of
miles (kilometers) away (Welch et al.
2007, p. 5).
Groundwater flows in a general
direction from Spring Valley to Snake
Valley. Thus, large-scale pumping in
Spring Valley is expected to impact
groundwater in Snake Valley. Current
groundwater pumping in Spring Valley
was estimated at 18,475 afy in 2007
(NSE 2007, p. 35). The additional 68,000
afy of groundwater pumping being
proposed would be a 368-percent
increase in total groundwater pumped
(NSE 2007, p. 56). The proposed total
amount (86,475 afy) is 93 percent of the
estimated 93,000 afy annual natural
recharge for the basin and 114 percent
of the estimated 76,000-afy annual
natural discharge of the basin (Welch et
al. 2007, p. 81).
Although current groundwater
pumping for all of Snake Valley (Nevada
and Utah) was estimated at 35,000 afy
in 2005, water rights are currently
allocated for 67,000 afy in Nevada
(12,000 afy) and Utah (55,000 afy)
(Welch et al. 2007, p. 81; Kikuchi and
Conrad 2009, p. 2). An additional
41,000 afy of groundwater pumping is
being proposed by the States of Nevada
and Utah in their interstate agreement.
This amount of additional groundwater
pumping would be in place of the
50,679 afy that the SNWA project
intends to pump, and would thus be a
61-percent increase in total groundwater
allocated for pumping (SNWA 2008, pp.
1-6, Tables 1-1). The proposed total
amount (108,000 afy) is 97 percent of
the estimated 111,000-afy annual
natural recharge for the basin and 82
percent of the estimated 132,000-afy
annual natural discharge of the basin
(Welch et al. 2007, p. 81; Kikuchi and
Conrad 2009, p. 2).
The BARCAS study included
assessments of the hydrogeology,
recharge, and discharge of groundwater
flow and geochemistry of 13
hydrographic areas in eastern Nevada
and western Utah, including the Spring
and Snake Valleys. The BARCAS study
estimated that the study-wide natural
average annual groundwater recharge
exceeded natural annual discharge by
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35407
about 90,000 afy (Welch et al. 2007, pp.
81-82). However, factoring in human
use of groundwater (80,000 afy) into this
estimate resulted in a nearly balanced
groundwater budget over the study area.
Thus, future long-term use of
groundwater at the current level or any
increased level (e.g., SNWA GWD
project) could decrease subsurface
outflow and spring discharge in the
foreseeable future (Welch et al. 2007, p.
82). The study concluded that
‘‘decreases in outflow would be more
likely in sub-basins having high
pumping and relatively large outflow,
such as in Snake Valley’’ (Welch et al.
2007, p. 82). As explained in the
previous section (Current Groundwater
Pumping), decreases in flow to some
springs have already occurred in Snake
Valley.
In addition to the BARCAS study, in
2007 the Utah State Legislature charged
the Utah Geological Survey with
conducting a 2–year study (West Desert
Groundwater Monitoring Project) to
characterize the background water
levels and chemistry; understand
regional flow in the carbonate and
basin-fill aquifer systems and their
connectivity; quantify future
groundwater drawdowns; and collect
data for future groundwater-flow models
(UGS 2008, entire). The groundwater
monitoring network in Utah’s west
desert should better define background
water levels and geochemical conditions
prior to SNWA pumping, and also be
able to help quantify changes after
pumping begins.
A lack of information exists on the
extent of the aquifers, their hydraulic
properties, and the distribution of water
levels that would contribute to a reliable
prediction of the amount or location of
drawdown, or the rate of change in
natural discharge, caused by pumping
(Prudic 2006, p. 3). Despite the lack of
site-specific information, we can
reasonably expect that additional
groundwater withdrawal in Spring and
Snake Valleys will directly reduce
spring discharge through reduced flows
from the shallow basin-fill aquifer or
through reduction of the hydraulic head
of the deep carbonate aquifer (Welch et
al. 2007, p. 82). As those flows become
increasingly disconnected, habitats lose
characteristics essential to aspects of
complex lifecycles, particularly the
reproductive requirements of least chub
(Deacon 2007, p. 3). Increases in
groundwater use above the 2005 levels
could significantly alter the hydrology
in areas surrounding least chub habitat
(Welch et al. 2007, p. 82).
The extent and timing of these effects
will vary among springs, based on their
distance from extraction sites and
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location relative to regional
groundwater flow paths (Patten et al.
2007, pp. 398-399). Some, and maybe
all, predictions of detrimental impacts
to the Snake Valley Hydrographic Basin
from groundwater pumping are likely to
occur (Kirby and Hurlow 2005, p. 33)
and are likely to significantly threaten,
and possibly eliminate, the remaining
least chub populations in Snake Valley
in the foreseeable future.
Prior to the completion of the SNWA
GWD Project, baseline data collection
and research on biologic and hydrologic
impacts will continue. Federal, State,
and county government agencies, as
well as nongovernmental organizations
and private interests, maintain a high
level of concern regarding negative
impacts to spring discharge rates, and
ultimately least chub habitats, from
groundwater pumping.
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Other Proposed Water Development
Projects
In addition to SNWA, other
municipalities are interested in
developing water resources in areas that
are potentially hydrologically connected
to least chub habitat. The following
information is provided to characterize
the additional potential threat of
groundwater development, but does not
at this time represent a clear threat to
least chub or their habitat. Actual effects
will, in part, be dependent on the degree
of connectivity of water developments
to least chub habitats.
On October 17, 2006, the Central Iron
County (Utah) Water Conservancy
District filed applications to appropriate
underground water in Hamlin Valley,
Pine Valley, and Wah Wah Valley in the
amounts of 10,000, 15,000, and 12,000
afy, respectively (UDWRi 2009a, pp. 2,
12, 23). The principal use of this
applied-for water is municipal, with
minor amounts used for stock watering
(UDWRi 2009a, entire). To date, the USE
has not acted upon these applications.
Similarly, Beaver County, Utah,
purchased water right applications in
2007 originally filed on October 6, 1981,
for Wah Wah, Pine, and Hamlin Valleys
(UDWRi 2009b, pp. 2, 5, 8). A hearing
was held on December 10, 2008, on
these Beaver County (successor-ininterest) applications, and on September
14, 2009, these water rights were
rejected by the State Engineer (UDWRi
2009b, pp. 3, 6, 9). Lastly, the State of
Utah School and Institutional Trust
Lands Administration (SITLA) filed
applications for up to 9,600 afy from
underground water wells in the Snake
Valley (UDWRi 2009c, entire). These
water rights all occur in areas that are
hydrologically connected to Snake
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Valley and, thus, utilization of this
water could impact least chub habitat.
The Confederated Tribes of the
Goshute Reservation, located in eastcentral Nevada (White Pine County) and
west-central Utah (Juab and Tooele
Counties) is interested in developing
their as yet unused water rights. They
have a 1905 decreed surface water right
along the Deep Creek system in Utah
(Steele 2008, p. 2), and are currently
planning to increase Deep Creek basin
rights to provide for community
development projects (Steele 2008, p. 3).
They estimate that up to 50,000 afy will
be needed for beneficial uses including
expanded crop and livestock irrigation,
fishery management, surface water
reservoir operation and maintenance,
and water pipeline conveyance (Steele
2008, p. 3). The USE is currently
reviewing their application to develop
50,000 afy of water from the Deep Creek
Valley.
To conclude, we assessed the threat of
water withdrawal and diversion by
analyzing available information on
historic, current, and planned future
groundwater development. It is clear
that historic and current groundwater
withdrawal has impacted least chub and
caused population extirpations. Future
water withdrawals are a significant
threat to extant populations. Local
agriculture pumping and drought have
historically and are currently
diminishing springs and least chub
habitats in Snake Valley. Many historic
springs are permanently dry, largely
because of historic groundwater
withdrawal. New wells are being drilled
on a yearly basis, and the amount of
groundwater withdrawal is generally
increasing.
In 2008, the NSE approved a major
portion of the SNWA groundwater
rights applications for the Spring Valley
Hydrographic Basin. Current active
applications for groundwater
withdrawals in areas supporting least
chub include SNWA applications in
Snake Valley, and potential projects by
Central Iron County Water Conservancy
District, Beaver County, Utah, and the
Confederated Tribes of the Goshute
Reservation. Because of the
complexities of determining
groundwater budgets and the effects of
future pumping, it is not possible at this
time to determine the degree to which
least chub habitats would be affected by
groundwater pumping. However,
information on current groundwater
pumping indicates that groundwater
levels are generally decreasing in basins
or hydrographic areas with least chub,
and that future large-scale groundwater
pumping in or near the Snake Valley
populations of least chub is predicted to
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result in decreased subsurface outflow
and spring discharge in Snake Valley.
The Snake Valley contains the only
remaining naturally occurring and
relatively secure populations of least
chub. Our analysis indicates that
groundwater withdrawals will continue
to increase in the future and lead to a
decrease in suitable habitat for least
chub; this is a significant threat to the
species, now and in the foreseeable
future.
(6) Drought
Prolonged droughts have primary and
secondary effects on groundwater
resources. Decreased precipitation leads
to decreased recharge of aquifers.
Decreased surface-water resources
generally lead to increased groundwater
withdrawal and increased requests for
water-well construction permits (Hutson
et al. 2004, p. 40; Burden 2009, p. 2).
Past and future climatic conditions (See
Factor E. Climate Change) influence the
water available to both water
development and aquatic habitats, with
water development usually taking
priority.
The impacts to least chub habitat from
drought can include: reduction in
habitat carrying capacity; lack of
connectivity resulting in isolation of
habitats and resources; alteration of
physical and chemical properties of the
habitat, such as temperature, oxygen,
and pollutants; vegetation changes;
niche overlap resulting in hybridization,
competition, and predation; and
reduced size and reproductive output
(Alley et al. 1999, pp. 41, 43; Deacon
2007, pp. 1-2). These impacts are similar
to those associated with water
withdrawal and diversions as described
in Factor A.
Recently, the Utah and Nevada
portions of the Great Basin experienced
drought conditions from 1999 until
2004 (Lambert 2009, pers. comm.;
NDMC 2009, entire). The recent drought
is not unusual for its length, but is for
its severity; water year 2002 will be
recorded as one of the driest years on
record for many parts of the Great Basin
(Lambert 2009, pers. comm; NDMC
2009, entire).
Although it is not possible to separate
the effects of drought from the effects of
water withdrawal in order to analyze
each separately as a threat to the least
chub, the cumulative impacts of both
threats have impacted least chub
populations in the past. The cumulative
impact of drought and water
development for irrigation has led to the
loss of springs in the Snake Valley,
including those on the Bagley and
Garland Ranches (Garland 2007, pers.
comm.). More recently, a multiyear
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drought from 1999 to 2004 (Lambert
2009, pers. comm.; NDMC 2009, entire)
impacted least chub habitats, such as
the Gandy Salt Marsh (Wilson 2006, p.
8). At this site, UDWR observed the
reduction of least chub habitat from
springs drying up throughout the
complex (Wilson 2006, p. 8).
Although least chub have survived for
thousands of years with intermittent
natural drought conditions, recent
human settlement has exacerbated
drought conditions via human water use
(Hutson et al. 2004, p. 2). On its own,
drought is not considered a significant
threat to the species as this is a natural
condition with which least chub
evolved. However, the documented
extirpation and population reductions
of least chub caused by drought and
groundwater withdrawal, and plans for
future large-scale groundwater
withdrawal, lead us to conclude that
drought is a significant threat to least
chub.
Conservation Agreements
The LCCAS is the guiding document
for management of least chub (Bailey et
al. 2005, entire) by the multiagency
LCCT. Signatories to the LCCAS include
UDWR, the Service, BLM, BOR,
URMCC, the Confederated Tribes of the
Goshute Reservation, CUWCD, and
SNWA (Bailey et al. 2005, p. 2). The
LCCAS and the LCCT provide expertise,
recommendations, and coordination of
funding for the conservation of the
species, but do not provide regulatory
protection. In 1999, we withdrew a
proposed rule to list the least chub after
analyzing the LCCAS and determining
that the conservation actions contained
within afforded greater protection to the
least chub and rendered the existing
regulatory mechanisms adequate. We
revisit that determination here.
Numerous conservation actions
implemented through the LCCAS were
most recently summarized by UDWR
(Hines et al. 2008, entire). Annual
surveys and monitoring of least chub
have occurred since at least 1998 across
the species’ historic range. These
surveys resulted in the discovery of two
new populations of least chub at Mills
Valley and Clear Lake. In addition, the
surveys resulted in identification of a
few suitable reintroduction sites and the
establishment of refuge populations (as
discussed in the ‘‘Translocations’’
section above). Research efforts initiated
and directed by the LCCAS have
improved our knowledge of least chub
life history and genetic structure (Mock
and Miller 2005, p. 276; Mock and
Bjerregaard 2007, p. 146). The LCCT
was successful in securing land
acquisitions, easements, and water
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rights to partially protect least chub
populations and habitats at Mona
Springs, Bishop Springs, and Gandy Salt
Marsh. Habitat enhancement projects
have focused on nonnative vegetation
removal, grazing management, and
springhead and pond restorations.
Efforts are ongoing to control the
impacts of nonnative aquatic species,
such as mosquitofish, but to date these
methods have been largely unsuccessful
(for further discussion of nonnative
species see Factor D below).
The LCCAS has proved invaluable in
providing better information concerning
the least chub’s status and distribution,
and implementation of research under
the LCCAS has increased our
understanding of least chub life history,
genetics, and interactions with invasive
species (Hines et al. 2008, entire). The
LCCT has addressed several of the
factors previously thought to threaten
the least chub and has made substantial
progress on the threat of grazing and
direct habitat loss, as well as the
conservation of least chub genetics.
However, the participants signatory to
the Agreement have no ability to protect
the least chub from the primary threat
of loss of habitat due to groundwater
development and only limited ability to
protect the species from the threat of
nonnative fish introduction (Hines et al.
2008, entire). Limitations of the LCCAS
and its participants also include their
ability to manage livestock grazing on
private and SITLA lands.
Summary of Factor A
At this time, based on best available
information, we do not believe that
mining, and oil and gas leasing and
exploration, or urban and suburban
development significantly threaten least
chub now or in the foreseeable future.
However, loss of habitat has extirpated
least chub from all but a fraction of its
historical range primarily as a result of
development along the Wasatch Front
and water diversions throughout the
Bonneville Basin. Remaining least chub
populations are threatened by livestock
grazing (excluding the Clear Lake site)
and development of water resources for
agricultural practices and urban
development. We find that listing the
least chub as a threatened or endangered
species is warranted due to livestock
grazing; water withdrawal and
diversion; and drought occurring now
and in the foreseeable future.
Habitat at four of the five extant
populations of least chub is currently
impacted by livestock grazing. Although
fencing and limited livestock grazing
management have reduced or
eliminated many of the negative impacts
associated with this practice, impacts to
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35409
least chub habitat continue to result
from livestock grazing on private lands
or in areas where livestock grazing is
uncontrolled for short periods of time.
Grazing impacts continue to occur on an
intermittent basis at Leland Harris
Spring Complex, Gandy Salt Marsh,
Bishop Springs Complex, and Mills
Valley.
Three of the five extant populations of
least chub persist in close proximity to
one another in the Snake Valley and
occur within the same groundwater
basin, where they depend on springs
and associated wetlands. Additional
significant groundwater development is
expected to occur by 2028 for Spring
Valley and 2050 for Snake Valley with
the possibility of subsequent landscapelevel effects to Snake Valley and
remnant least chub populations.
It is difficult to predict the foreseeable
future regarding large-scale groundwater
withdrawal and resultant effects to least
chub. We expect that there may be a lag
time after pumping commences before
effects will be realized by the species or
measured by scientists. Because the
agreement that would manage
groundwater allocations in Snake Valley
is still in draft form, the groundwater
hydrology of the Snake Valley is not
well known, and the area is already
experiencing changes in water regime
due to the effects of water withdrawal,
drought, and climate change, we cannot
confidently predict when impacts from
water withdrawals will occur.
Therefore, we find the least chub is
threatened by the present or threatened
destruction, modification, or
curtailment of the species’ habitat or
range, now and in the foreseeable
future.
B. Overutilization for Commercial,
Recreational, Scientific, or Educational
Purposes.
Commercial, recreational, scientific,
and educational utilizations are not
common least chub related activities,
and protections are in place to limit
their effect on the species. Least chub
are considered a ‘‘prohibited’’ species
under Utah’s Collection Importation and
Possession of Zoological Animals Rule
(R-657-3-1), which makes it unlawful to
collect or possess least chub without a
permit. Over the past 8 years only two
permits were issued by UDWR for
survey of least chub in the wild. All fish
collected for these studies were released
unharmed (Wilson 2009b, p. 1). Use of
least chub for scientific or educational
purposes also is controlled by UDWR,
and the agency typically provides least
chub from fish hatchery stocks for these
purposes (Wilson 2009b, pp. 1-4.). The
UDWR has collected least chub from the
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wild (an average of 334 per year
combined for all extant populations for
the last 10 years) to augment hatchery
stocks or for transfer to new or existing
translocation sites (Wilson 2009b, pp. 23). We are aware of no evidence that
least chub are being illegally collected
for commercial or recreational purposes.
Summary of Factor B
Least chub are not being overutilized
for commercial, recreational, scientific,
or educational purposes. Fish that are
needed for research purposes can be
provided from fish hatchery stocks. A
limited number of least chub have been
collected from wild populations for
hatchery augmentation or for
translocation purposes, but we have no
information to suggest that this causes a
threat to extant populations now or in
the foreseeable future. We find that
overutilization for commercial,
recreational, scientific, or educational
purposes of the least chub is not a threat
now or in the foreseeable future.
C. Disease or Predation.
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Predation
Least chub rarely persist where
nonnative fishes have been introduced
(Osmundson 1985, p. 2; Hickman 1989,
pp. 2-3, 9). The species is tolerant of
broad natural habitat conditions and is
well adapted to persist in the extreme,
yet natural, environments of springs and
playa marshes of the Bonneville Basin,
but they are not an effective competitor
with nonnative species (Lamarra 1981,
p. 1), and are constantly threatened by
the introduction and presence of
nonnative fish (Hickman 1989, p. 10).
The mosquitofish is the most
detrimental invasive fish to least chub
(Perkins et al. 1998, p. 23; Mills et al.
2004b, entire). Mosquitofish predate on
the eggs and the smaller size classes of
least chub and compete with adults
(Mills et al. 2004b, p. 713). The
presence of mosquitofish changes least
chub behavior and habitat use because
young least chub retreat to heavily
vegetated, cooler habitats in an effort to
seek cover from predation. In these less
optimal environments, they have to
compete with small mosquitofish that
also are seeking refuge from adult
mosquitofish. This predatory refuge
scenario, in turn, affects survivorship
and growth of least chub young of year
(Mills et al. 2004b, pp. 716-717).
Mosquitofish tolerate an extensive
range of environmental conditions and
have high reproductive potential (Pyke
2008, pp. 171, 173). The ecological
impact of introduced mosquitofish is
well documented. Mosquitofish
profoundly alter ecosystem function,
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and several studies have demonstrated
their effects on the decline of native
amphibians and small fish (Alcaraz and
Garcia-Berthou 2007, pp. 83-84; Pyke
2008, pp. 180-181). The mosquitofish is
native only to the southern United
States and northern Mexico, but has
been introduced into more than 50
´
countries (Garcıa-Berthou et al. 2005, p.
453) to control mosquito populations
and malaria (Pyke 2008, p. 172).
Mosquito abatement districts
throughout Utah have released
mosquitofish for mosquito control since
1931 (Radant 2002, p. 2). The
mosquitofish have expanded into
aquatic ecosystems throughout Utah
(Sigler and Sigler 1996, pp. 227-229).
Despite extensive efforts that include
chemical poisoning and mechanical
removal, the elimination of
mosquitofish from least chub habitats
has not been successful. Mosquitofish
have contributed to the functional
extirpation of least chub populations at
the naturally occurring Mona Springs
site (Hines et al. 2008 pp. 35-37), and
contributed to the extirpation of least
chub at three translocation sites
including Walter and Deadman Springs
at Fish Springs National Wildlife Refuge
(Wilson and Whiting 2002, p. 4), and at
an Antelope Island pond (Thompson
2005, pp. 5-6).
The UDWR implemented a
Memorandum of Agreement (MOA)
with Mosquito Abatement Districts in
an effort to reduce the continued spread
of mosquitofish (Radant 2002, entire).
The MOA established administrative
processes and procedures for collecting,
holding, propagating, transporting,
distributing, and releasing mosquitofish
for signatory mosquito abatement
districts. Mosquito abatement districts
that did not sign the MOA are
prohibited from engaging in any
mosquitofish-related activities (Radant
2002, p. 1). The MOA restricts the use
of mosquitofish to locations approved
by the UDWR (Radant 2002, p. 5). The
MOA was established to function in
perpetuity, but any party to the
agreement can terminate their
involvement by providing 60 days’
written notice to the UDWR.
Termination by one or more parties will
not act to terminate the agreement to
other parties. Once a signatory
terminates their involvement in the
MOA, they are prohibited from engaging
in any mosquitofish activities (Radant
2002, p. 7). This policy is not expected
to change in the foreseeable future.
Other nonnative fishes predate upon
and compete with least chub. Rainwater
killifish (Lucania parva) and plains
killifish (Fundulus zebrinis) have been
illegally introduced into least chub
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habitats by unknown entities (Perkin et
al. 1998, p. 23). These fish are potential
competitors with the least chub because
they are closely related to mosquitofish
and have similar life histories and
habitat requirements (Perkins et al.
1998, p. 23).
Introduced game fishes, including
largemouth bass (Micropterus
salmoides), rainbow trout
(Oncorhynchus mykiss), common carp
(Cyprinus carpio), and brook trout
(Salvelinus fontinalis) are predators of
least chub, and these species are present
in both native and introduced least chub
habitats (Workman et al. 1979, pp. 1-2,
136; Osmundson 1985, p. 2; Sigler and
Sigler 1987, p. 183; Crist 1990, p. 5).
Clear Lake and Mills Valley least chub
populations are currently sympatric
with nonnative predators other than
mosquitofish. Rainbow trout and
common carp are present in Clear Lake
(Hines et al. 2008, p. 43). Clear Lake is
an expansive habitat that allows least
chub to temporarily coexist with
nonnative fishes, but least chub will
become increasingly vulnerable to
extinction if habitat size diminishes
(Deacon 2007, p. 2) or nonnative
numbers increase. Nonnative sunfish
(Lepomis sp.), which is a voracious
predator, and fathead minnow
(Pimephales promelas) (Sigler and
Sigler 1987, p. 306), are established at
the Mills Valley site and are increasing
in number (Hines et al. 2008, p. 43).
In summary, least chub are unlikely to
persist indefinitely in the presence of
nonnative species, particularly
mosquitofish. Mosquitofish are a
predator of least chub eggs and young,
and they compete with least chub for
food items. The presence of nonnative
predacious fish results in the decline
and eventual elimination of least chub
populations. The stocking of
mosquitofish into least chub habitat by
Statewide mosquito abatement programs
has been addressed by an MOA that
regulates this practice. Removing
mosquitofish from aquatic habitats has
not been successful, and they continue
to invade new sites. Four naturally
occurring or introduced least chub
populations have been extirpated by
mosquitofish (Hines et al. 2008 pp. 3537; Wilson and Whiting 2002, p. 4;
Thompson 2005, pp. 5-6). These include
the sites of Deadman and Walter
springs, Antelope Island, and Mona
Springs. Two of the five remaining least
chub populations (Mills Valley and
Clear Lake) are coexisting with
nonnative species. Therefore, we
determine that the continued existence
of least chub is threatened by the
presence of nonnative fish species and
their potential spread into least chub
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habitat. This threat will become
exacerbated in the future by any
reductions in water quantity that further
fragment and degrade the habitat.
Disease and Parasitism
Disease and parasitism have not
affected least chub to a significant
degree. Workman et al. (1979, pp. 2,
103-107) found the parasite blackspot
(Neascus cuticola) present in the least
chub population at the Leland Harris
Spring Complex site during 1977–78
sampling, and at the time determined
that all least chub examined appeared
robust and in good condition. More
recently, the parasite was identified in
least chub at the Bishop Springs site by
Wheeler et al. (2004, p. 5). Although we
have no information that allows us to
determine the effect of blackspot on
least chub at the Bishop Springs site,
monitoring over the past 14 years
indicates that the population has
remained stable (Hines et al. 2008, pp.
37-39).
The exotic snail Melanoides
tuberculata is an intermediate host and
vector for parasites known to be
dangerous to humans, livestock, and
wild animals, including threatened
endemic fishes and amphibians (Rader
et al. 2003, p. 647). M. tuberculata
occurs at the Bishop Springs and Clear
Lake sites, but we do not have any
information that links this snail species
to parasites that are harmful to least
chub (Rader et al. 2003, p. 649). M.
tuberculata appears to be restricted by
water temperature, but has the potential
to be found in other least chub habitats
in the future, because sampling for M.
tuberculata has not occurred at all
known least chub sites (Rader et al.
2003, pp. 650-651).
In 2006, least chub from the Leland
Harris Spring Complex population were
subjected to a disease-check regimen at
the Fisheries Experiment Station in
Logan, Utah. Eight different parasites
were detected on the fish; however, it
was the opinion of LCCT that the
presence of these parasites is common
on a seasonal basis for most wild
populations of least chub (Wilson
2009b, p. 4). Considering that least chub
are the dominant fish species at the
Leland Harris Spring Complex site and
that their population appears stable
(Hines et al. 2008, p. 42), these diseases
are likely having a minimal effect on the
species.
Although parasites exist in least chub
habitats, and some least chub have been
found to harbor parasites, we do not
have evidence that individual least chub
or least chub populations are
significantly compromised or threatened
by the presence of parasites.
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Summary of Factor C
At this time, we know of no
information that indicates that the
presence of parasites or disease
significantly affects least chub, now or
in the foreseeable future.
There is strong evidence that least
chub are threatened by the presence of
nonnative fish species in their habitats.
Populations of least chub that are
sympatric with nonnative fish have
become extirpated or functionally
extirpated, and extant populations
generally decline when in the presence
of nonnative fish, especially
mosquitofish. The MOA with the
mosquito abatement districts is a
positive step toward prohibiting the
spread of mosquitofish in least chub
habitats. Although hatchery stocks
provide a source for reintroductions,
removal of nonnative fish has not been
successful; sites previously used for
translocation sites have had limited
success; and very few new sites that are
appropriate for least chub introductions
are available. Based on the best
scientific and commercial information
available to us, we conclude that
nonnative fish predation of least chub is
a threat to the continued existence of
the species, now and in the foreseeable
future.
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 least chub in danger
of becoming either threatened or
endangered. Regulatory mechanisms
affecting the species fall into four
general categories: (1) Land
management, (2) State mechanisms, (3)
Federal mechanisms, and (4)
conservation agreements.
(1) Land Management
Wild populations of least chub are
distributed across private, BLM, SITLA,
and State UDWR lands and incur
varying regulatory mechanisms
depending on land ownership.
(1) Mona Springs: Habitat in the
vicinity of Mona Springs was primarily
private land (Wilson 2009c, pers.
comm.). However, the URMCC acquired
34.6 ha (85.5 ac) in 1998 and 7.2 ha
(17.7 ac) in 2006 for the protection of
least chub and Utah State sensitive
species the Columbia spotted frog (Rana
lutreiventris) (Hines et al. 2008, p. 34).
The URMCC has recently purchased and
protected an additional 44.5 ha (18 ac)
of land on the north end of the spring
complex (Wilson 2009c, pers. comm.).
The amount of habitat owned and
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managed by URMCC provides
protection from direct habitat loss.
However, land ownership by URMCC
cannot protect the springs from loss of
water caused by groundwater pumping
or from the threat of nonnative fish that
are now at this site.
(2) Leland Harris Spring Complex:
Land ownership for least chub occupied
habitat is primarily private although
there also has been occupied habitat on
nearby SITLA and BLM land (Hines et
al. 2008, pp. 41-42; Jimenez 2009, pers.
comm.; Wilson 2009c, pers. comm.).
Miller Spring (located in this complex)
and surrounding wetlands
(approximately 20.2 ha (50 ac)) are
protected through a conservation
easement between UDWR and a private
landowner. This level of land
management provides some protection
through cooperative grazing
management under the conservation
easement; however, impacts resulting
from livestock grazing still occur (see
Factor A. Livestock Grazing). There also
is some protection provided through
Federal land management under the
BLM RMP and future energy lease
notices (See Factor A. Mining, and Oil
and Gas Leasing and Exploration).
However, existing land management
does not protect the site from loss of
water due to groundwater pumping or
the possibility of nonnative fish
invasion. We are unaware of any land
management protection mechanisms on
SITLA lands.
(3) Gandy Salt Marsh: Land
ownership includes BLM, SITLA, and
private lands (Wilson 2009c, pers.
comm.). The BLM has designated 919 ha
(2,270 ac) as an Area of Critical
Environmental Concern (ACEC) that is
closed to oil and gas leasing to protect
the least chub. The ACEC includes most
of the lake bed and aquatic habitats and
is fenced to exclude livestock (BLM
1992, pp. 11, 16, 18). This level of land
management is adequate to protect the
site from human-caused impacts
associated with energy development
and livestock grazing on Federal lands,
but does not protect the habitat on
SITLA or private lands. In addition,
there is not protection from the loss of
water due to groundwater pumping or
the possibility of nonnative fish
invasion.
(4) Bishop Springs Complex: Land
ownership is primarily private, but
includes SITLA and BLM lands (Wilson
2009c, pers. comm.). In 2006, UDWR
purchased water rights from the
landowner for Foote Reservoir and
Bishop Twin Springs (a.k.a. Bishop
Small Springs) (Wilson 2009c, pers.
comm.). These water bodies provide
most of the perennial water to the
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complex (Hines et al. 2008, p. 37). In
2008, UDWR obtained a permit for
permanent change of use from the USE
for instream flow according to a
seasonal schedule. This instream flow
helps to maintain water levels at Bishop
Springs Complex, protecting the least
chub and Columbia spotted frog
populations (Hines et al. 2008, p. 37).
The UDWR-owned instream flow water
rights may protect least chub
populations in this area from loss of
water due to existing private landowner
uses. However, this level of land
management cannot protect for the
possibility of nonnative fish invasion or
impacts associated with livestock
grazing on private lands, and it may not
be adequate to protect the site from the
indirect loss of water associated with
future large-scale groundwater
pumping. We are unaware of any land
management protection mechanisms on
SITLA lands.
(5) Mills Valley: Most of the Mills
Valley site is privately owned, and no
management agreements are in place.
The UDWR is working with landowners
to improve the current grazing
management plans (Hines et al. 2008, p.
43). Approximately 36.4 ha (90 ac) is
owned by UDWR as the Mills Meadow
WMA (Wilson 2009c, pers. comm.).
Livestock grazing rights at this WMA are
awarded to adjacent landowners in
exchange for public and UDWR access
to their property (Stahli and Crockett
2008, p. 5). The limited amount of
habitat owned by UDWR provides some
protection from direct habitat loss and
other direct human-caused impacts, and
UDWR’s efforts to work with private
landowners may provide protection on
some private land. However, this level
of land management cannot protect the
area from all impacts associated with
livestock grazing (see Factor A.
Livestock Grazing), loss of water caused
by groundwater pumping, or from the
threat of nonnative fish that are now at
this site.
(6) Clear Lake: This population occurs
on the Clear Lake WMA, which is
managed by UDWR (Wilson 2009c, pers.
comm.). The land owned and managed
by UDWR provides protection from
direct habitat loss associated with
human land-uses, including livestock
grazing. However, this level of land
management cannot protect the area
from loss of water caused by
groundwater pumping or from the threat
of nonnative fish that are now at this
site.
(2) State Mechanisms
Least chub are considered
‘‘prohibited’’ species under the Utah
Collection Importation and Possession
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of Zoological Animals Rule (R-657-3-1),
making them unlawful to collect or
possess. These species receive
protection from unauthorized collection
and take. While its classification is not
a regulatory mechanism, the least chub
is classified in the State of Utah Wildlife
Action Plan as a Tier 1 Sensitive
Species, a status that includes federally
listed species and species for which a
conservation agreement has been
completed and implemented (Bailey et
al. 2005, p.3). This classification
includes species for which there is
credible scientific evidence to
substantiate a threat to continued
population viability.
Introduced nonnative fishes for
mosquito abatement and game-fishing
purposes can be detrimental to the
persistence of least chub (see Factor C.
Predation). The UDWR follows their
Policy for Fish Stocking and Transfer
Procedures and no longer stocks
nonnative fish into least chub habitat
(Hines et al. 2008, p. 25). This Statewide
policy specifies protocols for the
introduction of nonnative species into
Utah waters and states that all stocking
actions must be consistent with ongoing
recovery and conservation actions for
State of Utah sensitive species,
including least chub. This policy is not
expected to change in the foreseeable
future.
Mosquito abatement districts are not
prohibited from spraying least chub
habitat to control for mosquitoes. This
practice has the potential to reduce least
chub prey items, and it may negatively
affect potential reintroduction sites. The
BLM has rejected a Juab County
(location of Mills Valley and Leland
Harris Springs Complex least chub
populations) request to implement a
mosquito-control spraying program in
marsh and spring areas on BLMadministered lands; however, this does
not prevent the county from spraying on
privately owned lands (Perkins et al.
1998, p. 24).
In summary, abatement districts may
be having an effect on least chub
populations by spraying to reduce
mosquito larvae. On the basis of the
information we have at this time, we do
not believe that mosquito spraying is
having a significant effect on least chub
at an individual or population level. As
a result, we do not find that it is a
significant threat to the species.
The State of Utah operates under
guidelines to prevent the movement of
aquatic invasive species, including
quagga mussels (Dreissena sp.), zebra
mussels (Dreissena sp.), and mud snails
(Potamopyrgus sp.) during fish transfer
operations (UDWR 2009, entire).
Protocols include notification and
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evaluation of water sources being
considered for fish transfers, fish health
inspections, and completion of an
updated Hazard Analysis and Critical
Control Point Plan. These protocols
should help reduce the probability of
additional aquatic invasive species
introductions to least chub habitats.
Regulatory mechanisms that relate to
historic groundwater withdrawal are
implemented through the USE through
the UDWRi, the Lincoln County Water
Conservancy District, and the Central
Iron County Water Conservancy District
as described in Factor A. Water
Withdrawal and Diversion section.
Groundwater withdrawal in the Snake
Valley for future municipal
development is subject to both Federal
and State regulatory processes. The
LCCRDA directed a study of
groundwater quantity, quality, and flow
characteristics in Utah and Nevada
counties, and the Utah State Legislature
requested a study on groundwater
recharge and discharge to better
determine effects of planned
groundwater withdrawal. The SNWA
may begin pumping groundwater for a
portion of their proposed projects prior
to completion of the study that will help
better disclose effects of the action. A
lack of data on effects of groundwater
withdrawal to least chub is a concern,
and the ability of water districts to
effectively manage groundwater to avoid
impacts to least chub populations has
not been demonstrated. (See Factor A.
Water Withdrawal and Diversion for
more detail.) Therefore, we find that the
State regulatory mechanisms in
existence do not adequately protect the
least chub from the threat of reduction
of habitat due to water development
projects.
(3) Federal Mechanisms
The major Federal mechanisms for
protection of least chub and its habitat
are through section 404 of the Clean
Water Act (33 U.S.C. 1251 et seq.)
permitting process and the National
Environmental Policy Act (42 U.S.C.
4231 et seq.) (NEPA). Various Executive
Orders (11990 for wetlands, 11988 for
floodplains, and 13112 for invasive
species) provide guidance and
incentives for Federal land management
agencies to manage for habitat
characteristics essential for least chub
conservation.
The primary Federal land
management entity across the range of
extant least chub populations is the
BLM. The least chub is designated as a
sensitive species by the BLM in Utah.
The policy in BLM Manual 6840-Special
Status Species Management states:
‘‘Consistent with the principles of
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multiple use and in compliance with
existing laws, the BLM shall designate
sensitive species and implement species
management plans to conserve these
species and their habitats and shall
ensure that discretionary actions
authorized, funded, or carried out by the
BLM would not result in significant
decreases in the overall range-wide
species population and their habitats’’
(BLM 2008, p. 10).
The NEPA has a provision for the
Service to assume a cooperating agency
role for Federal projects undergoing
evaluation for significant impacts to the
human environment. This includes
participating in updates to RMPs. As a
cooperating agency, we have the
opportunity to provide
recommendations to the action agency
to avoid impacts or enhance
conservation for least chub and its
habitat. For projects where we are not a
cooperating agency, we often review
proposed actions and provide
recommendations to minimize and
mitigate impacts to fish and wildlife
resources.
Acceptance of our NEPA
recommendations is at the discretion of
the action agency. The BLM land
management practices are intended to
ensure avoidance of negative effects to
species whenever possible, while also
providing for multiple-use mandates;
therefore, maintaining or enhancing
least chub habitat is considered in
conjunction with other agency
priorities.
As described in Factor A, BLM
designated the Gandy Salt Marsh as an
ACEC, and it is closed to oil and gas
leasing (Jimenez 2009, pers. comm.). In
addition, the Fillmore Oil and Gas
Environmental Assessment provides
lease notices that can protect least chub
and their habitats. We conclude in
Factor A that oil and gas recovery on
BLM lands near least chub habitats is
anticipated to occur at a slow rate and
is not considered a significant threat
now or in the foreseeable future. The
aforementioned lease notices and other
potential RMP protection measures will
thus be beneficial for site-specific
management; however, we do not
anticipate a significant threat from
activities on BLM lands to the existence
of the least chub. Therefore, we find that
the current regulatory structure for oil
and gas leasing is adequate to protect
least chub and its habitat from this
potential threat.
Least chub population areas contain
wetland habitats, and section 404 of the
Clean Water Act regulates fill in
wetlands that meet certain jurisdictional
requirements. Activities that result in
fill of jurisdictional wetland habitat
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require a section 404 permit. We can
review permit applications and provide
recommendations to avoid and
minimize impacts and implement
conservation measures for fish and
wildlife resources, including the least
chub. However, incorporation of Service
recommendations into section 404
permits is at the discretion of the U.S.
Army Corps of Engineers. In addition,
not all activities in wetlands involve fill
and not all wetlands are ‘‘jurisdictional.’’
Regardless, we have evaluated threats to
the species’ habitat where fill of
wetlands may occur, including peat
mining and oil and gas development. At
this time we do not have information to
indicate that this is at a level that
threatens the species now or in the
foreseeable future.
Summary of Factor D
We find that regulatory mechanisms
related specifically to land management
are sufficient for mitigating potential
threats from land development to the
least chub at four of the population
sites: Mona Springs (URMCC land
acquisition), Gandy Salt Marsh (BLM
ACEC), Bishop Springs (protection of
water rights), and Clear Lake (UDWR
WMA). The UDWR continues to work
with landowners at Mills Valley and the
Leland Harris Spring Complex to
implement beneficial grazing practices
and maintain fences; however, because
livestock-grazing-related impacts are
still observed at most extant least chub
sites, we determined that grazing is
considered a significant threat to the
least chub (see Factor A. Livestock
Grazing).
The BLM has provided protective
mechanisms in the form of lease notices
for conservation agreement and
sensitive species, including the least
chub, which can minimize impacts from
oil and gas drilling. We also retain the
ability to comment on NEPA
evaluations for other projects on BLM
lands that may impact the least chub.
We determined that oil and gas drilling
is not a threat to the least chub given the
low level of expected energy
development in the area (see Factor A.
Mining, and Oil and Gas Leasing and
Development).
Regulatory mechanisms are not in
place to sufficiently protect the least
chub from local or large-scale
groundwater withdrawal. See Factor A
for more information regarding water
rights and proposed groundwater
withdrawal.
Although mosquito spraying is not
prevented by regulatory mechanisms,
we have no information indicating that
mosquito spraying is a significant threat
to the least chub.
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We find that the inadequacy of
existing mechanisms to regulate
groundwater withdrawal is a threat now
and in the foreseeable future for the
least chub.
E. Other Natural or Manmade Factors
Affecting Its Continued Existence.
Natural and manmade threats to the
species include: (1) hybridization; (2)
loss of genetic diversity; (3) stochastic
disturbance and population isolation;
(4) drought and climate change; and (5)
cumulative effects.
(1) Hybridization
Hybridization can be a concern for
some fish populations. An introgressed
population results when a genetically
similar species is introduced into or
invades least chub habitat, the two
species 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 (Schwaner
and Sullivan 2009, p. 198). 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 (Miller
and Behnke 1985, p. 514).
Hybridization is commonly associated
with disturbed environments (Hubbs
1955, p. 18). In complex habitats,
reproductive isolator mechanisms can
be eliminated as a result of habitat
alteration and degradation, and
resultantly, overlaps of reproductive
niches and breakdowns of behavior
occur due to overcrowding (Crawford
1979, p. 74; Lamarra 1981, p. 7). The
Bonneville Basin has suffered major
alterations to its aquatic environments,
including loss of habitat through water
diversions (Sigler and Sigler 1987, p.
39). Disturbances allow dispersal of
species to habitats where they did not
naturally occur. Water diversions may
allow isolated springs that previously
held distinctly separate populations
(allopatric) to overlap habitats
(sympatry) and present an opportunity
for hybridization to occur. Habitats such
as playa marshes of the Utah west desert
may become restricted to spring heads
as a result of water diversion, drought,
and climate change. Inadequate habitat
diversity forces sympatric species into
close spawning proximity.
Hybridization is even more likely since
least chub are broadcast spawners for an
extended period of time, and this
timeframe can overlap with the
spawning period of other species,
including the native Utah chub and
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speckled dace (Crawford 1979, p. 74;
Miller and Behnke 1985, p. 509).
A morphometric study of specimens
collected in 1977 and 1978 documented
hybridization of least chub with Utah
chub (Gila atraria) and speckled dace
(Rhinichthys osculus) at five locations
(Workman et al. 1979, pp. 156-158;
Miller and Behnke 1985, p. 510). Least
chub populations no longer occur at
three of these locations, and the other
two – Gandy Salt Marsh and Bishop
Springs (documented as Foote Reservoir
at the time) – are relatively healthy least
chub populations that had no evidence
of hybridization in genetic samples
collected in 1997. Although no
hybridization-specific studies have been
conducted on least chub, recent genetic
investigations have not documented
hybridization in extant least chub
populations (Mock and Miller 2003, p.
10).
In summary, most habitats where least
chub hybrids were found in the late
1970s consisted of altered systems that
lacked the complexity required for
reproductive isolation. Least chub no
longer occur at three of these sites, and
no new evidence of hybridization has
surfaced for the other two extant
locations. Despite the recorded
incidence of hybridization in the past,
there are no known new occurrences.
Therefore, hybridization is not
considered a significant threat to the
least chub now or in the foreseeable
future.
(2) Loss of Genetic Diversity
The level of genetic diversity in
individual fish populations influences
survival and adaptability to
environmental change. Maintaining
sufficient levels of genetic diversity
within all least chub populations is
important, primarily because they exist
in small, isolated populations compared
to the once-expansive historical
populations of Lake Bonneville.
Maintaining genetic diversity in refugia
and source populations is important as
well.
The patterns of genetic divergence
and diversity within and among
populations were described for five of
the six naturally occurring least chub
populations (six including the
population now functionally extirpated
at Mona Springs), representing three of
the known locations (Snake Valley and
Mona Springs in the Great Salt Lake
subbasin, and Mills Valley in the Sevier
subbasin) (Mock and Miller 2005, pp.
273-275). The analysis included
amplified fragment-length
polymorphism analysis and
mitochondrial DNA sequencing.
Pronounced, but temporally shallow,
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genetic structuring among these three
locations was apparent and consistent
with patterns of recent and historical
hydrogeographic isolation. The most
genetically divergent population in this
analysis was in Mona Springs, at the
extreme southeastern reach of the Great
Salt Lake subbasin, followed by the
Mills Valley population in the Sevier
subbasin. The three Snake Valley
populations (Leland Harris Spring
Complex, Gandy Salt Marsh, and Bishop
Springs) were genetically similar, which
is expected due to their spatial
proximity. The sixth and southernmost
population at Clear Lake was not
included in the initial analyses (Mock
and Miller 2005, pp. 273-275), but later
analysis indicated that the population is
most similar to the Mills Valley
population, which is consistent with
their location in the Sevier subbasin.
The Clear Lake population was distinct
from, and possibly more diverse than,
the Mills Valley population (Mock and
Bjerregaard 2007, p. 146).
Genetic diversity within naturally
occurring least chub populations
appears to be healthy with respect to
molecular diversity (Mock and Miller
2005, pp. 273-275). Gandy Salt Marsh
and Leland Harris Spring Complex
contain the highest diversity. This
suggests that: (1) These least chub
populations are large enough to avoid
significant historical genetic drift as
their populations become more isolated
from each other; or (2) these populations
have been historically large, and their
recent decline has been so rapid that the
loss of population genetic diversity is
not yet detectable. Genetic drift affects
the genetic makeup of the population
but, unlike natural selection, through an
entirely random process. So although
genetic drift is a mechanism of
evolution, it does not work to produce
adaptations. Thus, genetic drift may
rapidly reduce population-level genetic
diversity if populations stay small or are
subject to continued bottlenecks (Mock
and Miller 2005, p. 276).
Translocated populations in Lucin
and Walter Springs maintained the
genetic identity of their source
populations (Gandy Salt Marsh and
Leland Harris Spring Complex for Lucin
Springs, and Leland Harris Spring
Complex for Walter Springs) and
showed no evidence of a genetic
bottleneck (Mock and Miller 2005, pp.
273-275). However, this result is not
unusual because these translocated
populations were separated from their
source populations for only a few
generations. Bottlenecks in confined,
strong-source, and refugial populations
can lead to adaptive divergence that is
not yet detectable with genetic
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techniques but may be reflected in
behavioral changes and habitat
adaptations as a result of the hatchery
environment. These may cause a loss of
fitness in naturally occurring
populations if refugia and source
individuals are used in a supplemental
capacity (Mock and Miller 2005, pp.
273-275).
In summary, we find that extant wild
least chub natural populations show
adequate genetic diversity to sustain
healthy populations, and bottlenecks are
not apparent in wild, transplanted, or
hatchery populations. As described in
part (3) of this section, refugia exist for
four of the five persisting wild sites, and
these can provide supplementation to
the genetic pools of individual
populations if necessary.
(3) Environmentally Stochastic
Disturbance and Population Isolation
Environmentally stochastic events can
include several types of natural events,
such as drought, wildfire and its
resultant effects, or flood. Least chub
populations could be affected by
drought, especially when exacerbated
by water withdrawal or, potentially,
climate change. We address climate
change in part (4) of this section.
Least chub populations are isolated,
both naturally and as the result of
human impacts. Habitat connectivity is
absent among the three east/southeast
Bonneville Basin populations, and the
west desert populations are similarly
disconnected except in years of
exceptionally high water (Perkins et al.
1998, p. 23). We have no evidence of
least chub populations being affected by
fire or its resultant effect such as
siltation; however, one translocated
population was eliminated by flooding
of the Great Salt Lake (see Translocation
section).
Translocated least chub populations
can successfully maintain genetic
diversity of wild populations (Mock and
Miller 2005, pp. 273-277). Refuge or
hatchery populations are established for
three (Bishop Spring Complex, Mills
Valley, and Clear Lake) of the five extant
least chub populations as well as for the
functionally extirpated Mona Springs
population (Hines et al. 2008, pp. 3450). Until management measures can be
implemented to increase the quantity
and quality of new sites and existing
habitats, refuge populations provide a
source of genetic material that stores
adaptive differences not detectable with
molecular markers that may vary within
populations. These might include
habitat quality parameters, seasonal
temperature regimes, life-history traits,
and morphology (Mock and Miller 2003,
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pp. 18-19; Mock and Bjerregaard 2007,
p. 146).
In summary, loss of connectivity
resulting in small, genetically isolated
populations is a concern and requires
ongoing monitoring; however, genetic
stocks from four wild least chub
populations are available from
established refugia to augment the gene
pools of extant populations and prevent
genetic bottlenecks. Therefore, we have
determined that environmentally
stochastic disturbance and population
isolation is not considered a threat to
the least chub now or in the foreseeable
future.
(4) Climate Change
The groundwater flow system
encompassing least chub habitat is
affected by natural climatic conditions,
primarily precipitation and temperature
(Welch et al. 2007, p. 37). Least chub
have evolved in the Great Basin desert
ecosystem, demonstrating their ability
to withstand historical climatic
variability, including drought
conditions (Hines et al. 2008, pp. 19,
26). However, under future climatic
conditions and the added pressure of
human water consumption, these
evolutionary adaptations may not be
adequate to guarantee long-term
survival of least chub populations.
Climate variability adds uncertainty
to predictions of water recharge and
availability of natural aquifers (Welch et
al. 2007, p. 48). Predictions of future
climatic conditions can no longer rely
on analysis of past climatic trends, but
must instead take into account
predicted global climate change.
Therefore, it is important to consider
how future climatic conditions may
impact least chub. Both the IPCC and
the U.S. Global Climate Change Program
conclude that changes to climatic
conditions, such as temperature and
precipitation regimes, are occurring and
are expected to continue in western
North America over the next 100 years
(Parson et al. 2000, p. 248; Smith et al.
2000, p. 220; Solomon et al. 2007, p. 70
Table TS.6; Trenberth et al. 2007, pp.
252-253, 262-263). In western North
America, surface warming corresponds
with reduced mountain snowpack (Mote
et al. 2005 and Regonda et al. 2005,
cited in Vicuna and Dracup 2007, p.
330; Trenberth et al. 2007, p. 310) and
a trend toward earlier snowmelt
(Stewart et al. 2004, pp. 217, 219, 223).
Utah has experienced about 1.6 °C
(2.9 °F) of warming over the last 100
years (1908–2007) (Saunders et al. 2008,
p. 44). Modeling of future climate
change for Utah projects the State to
warm more than the average for the
entire globe, with fewer frost days,
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longer growing seasons, and more heat
waves (UBRAC 2007, p. 2). Although
exact temperature increases are not
known, projected temperature rise in
the southwestern United States by 2050
ranges between 1.4 and 2.0 °C (2.5 and
4.5 °F) for a lower emissions scenario,
and between 2.5 and 3.1 °C (3.5 and 5.5
°F) for a higher emissions scenario
(USGCRP 2009, p. 129).
Precipitation models predict a
reduction in mountain snowpack, a
threat of severe and prolonged episodic
drought (UBRAC 2007, p. 3), and a
decline in summer precipitation across
all of Utah (p. 18). However, Utah is in
the transition zone for predicted
changes in winter precipitation
(between the northwest and southwest
United States), resulting in low
confidence in future winter
precipitation trends (UBRAC 2007, p
18).
More locally to least chub, the
hydrology of the Great Salt Lake Basin
will be impacted by changes in
mountain runoff (UBRAC 2007, p. 18).
While predictions indicate that the
Great Salt Lake Basin will be affected by
declining mountain snowpack and the
resulting runoff, the timing and extent
of these changes are unclear (UBRAC
2007, p. 19). Drought conditions and
higher evaporation rates result in
lowered groundwater levels, reduced
spring flows, and reductions in size and
depth of pool habitat for least chub
(Wilson 2006, p. 8). Although current
data and climate predictions do not
indicate the exact nature of future
changes to extant least chub habitat
sites, we can assume that similar effects
will be likely.
Because the least chub depends on
small, ephemeral springfed wetlands for
major portions of its life history
(spawning, nursery niches, and feeding)
and the amount of this habitat available
will likely be reduced and restricted to
spring heads, the severity of climate
change is an important factor in the
species’ persistence. Under
circumstances of restricted habitats,
both hybridization and extirpation have
occurred (Hubbs 1955, p. 18; Miller and
Behnke 1985, p. 514). Additionally, the
species is bound by dispersal barriers
throughout its range and cannot retreat
to additional habitats or easily
recolonize areas after they have been
extirpated.
Despite the clear evidence that
climate change has had an effect on
temperature over the last 100 years, as
well as its potential causal association
with more intense drought conditions
that were experienced in the
southwestern United States over the last
decade (see Factor A. Drought), the
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35415
information available to us at this time
does not suggest that climate change
alone is a significant threat to least
chub. While climate change is likely to
have affected aquatic resources to some
extent in the past, including habitat
used by least chub, at this time our
analysis indicates that groundwater
withdrawal historically caused a more
significant long-term impact and that
separating the effects of climate change
from those of groundwater withdrawal
is not possible. Likewise, we determine
that groundwater withdrawal will be the
overriding impact to least chub in the
foreseeable future.
(5) Cumulative Effects
We cannot completely predict the
cumulative effects of climate change,
current and future groundwater
withdrawal, and drought on least chub
at this time, but we know that each will
occur to some extent and be
compounded by the others. At least five
Snake Valley populations, and as many
as 15 springs of occupied least chub
sites, have been extirpated in the last 30
years as a result of drought or irrigation
practices (see previous sections,
Historical Occurrences and Current
Distribution). Snake Valley harbors the
last remaining native habitats and the
last three naturally occurring least chub
populations that are not severely
impacted by nonnative fish and
urbanization.
The effects of proposed large-scale
groundwater withdrawal as described in
Factor A are likely to compound the
effects that localized groundwater
development has had on least chub. As
described above, past water
development in localized areas has
resulted in drying of least chub habitat
and the extirpation of the species from
these habitats. Extant least chub habitats
will likely be impacted by reduced
water and consequently wetted area and
wetland habitat reductions will result
from these threats individually, and will
be compounded cumulatively with
drought and climate change. The
cumulative effect of these three threats
will likely intensify the probable effects
described in Factor A: Water
Withdrawal and Diversions, Drought,
and Factor E: Climate Change.
In summary, we find that the
potential combinations of drought,
current and future groundwater
withdrawal, and climate change are
likely to occur and be significant threats
to least chub in the foreseeable future.
Significant effects have already occurred
as a result of drought and water
diversions, and least chub populations
in Snake Valley have been extirpated.
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Summary of Factor E
We assessed the potential risks of
hybridization, loss of genetic diversity,
and environmentally stochastic
disturbance to least chub populations.
Limited hybridization was documented
in the late 1970s at five sites; however,
least chub are no longer found at these
sites or recent genetic analysis shows
that hybridization is no longer an issue
for extant populations. Levels of genetic
diversity are appropriate to sustain least
chub populations, and genetic refuges
exist for three of five extant populations.
The available information does not
suggest that environmentally stochastic
disturbance threatens extant least chub
populations, and if necessary, refugia
populations are available to augment
existing populations. Based on the best
scientific and commercial information
available, we conclude that least chub is
not, now or in the foreseeable future,
threatened by hybridization, loss of
genetic diversity, or environmentally
stochastic disturbance.
Least chub have persisted for
thousands of years, and naturally
occurring drought does not significantly
threaten the species. Climate models
predict that the State may warm more
than average, with more heat waves, less
mountain snowpack, and a decline in
summer precipitation. It also is clear
that historic and current water
withdrawal, combined with the effects
of drought, have had significant
negative effects on least chub. It is
anticipated that these phenomena will
combine to reduce the quality and
quantity of least chub habitat, and that
when combined with the effects of
climate change, these three factors will
significantly threaten the least chub.
Therefore, we find that the least chub
is at risk of extinction now and in the
foreseeable future because of the
cumulative effects of climate change,
current and future groundwater
withdrawal, and drought.
It is difficult to predict the foreseeable
future regarding the cumulative effects
of climate change, groundwater
withdrawal, and drought and their
resultant effects to least chub. Drought
is a natural event that could happen at
any time and is, therefore, a factor
considered for the foreseeable future.
Current estimates for climate change are
most accurate for change in
temperature, but not precipitation; and
climatic models are generally accurate
to about 2030 for this parameter
(Solomon et al. 2007, p. 74). Thus, for
cumulative effects of climate change,
groundwater withdrawal, and drought,
it is anticipated that large-scale
groundwater pumping will be the
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overriding factor now and in the
foreseeable future.
Finding
As required by the Act, we considered
the five factors in assessing whether the
least chub is threatened or endangered
throughout all or a significant portion of
its range. We have carefully examined
the best scientific and commercial
information available regarding the past,
present, and future threats faced by the
least chub. We reviewed the petition,
information available in our files, other
available published and unpublished
information, and we consulted with
recognized least chub experts and other
Federal, State, and tribal agencies. In
considering what factors might
constitute threats, we must look beyond
the mere exposure of the species to the
factor to determine whether the species
responds to the factor in a way that
causes actual impacts to the species. If
there is exposure and the species
responds negatively, the factor may be
a threat and we then attempt to
determine how significant a threat it is.
If the threat is significant, it may drive
or contribute to the risk of extinction of
the species such that the species
warrants listing as threatened or
endangered as those terms are defined
by the Act.
On the basis of the best scientific and
commercial information available, we
find that listing of the least chub as
threatened or endangered is warranted.
We will make a determination on the
status of the species as threatened or
endangered when we do a proposed
listing determination. However, as
explained in more detail below, an
immediate proposal of a regulation
implementing this action is precluded
by higher priority listing actions, and
progress is being made to add or remove
qualified species from the Lists of
Endangered and Threatened Wildlife
and Plants.
Review of least chub historic
population trends shows that the
current distribution of the least chub is
highly reduced from its historic range.
In the late nineteenth century, least
chub were very common in tributaries
to Sevier, Utah, and the Great Salt Lakes
and for the next 50 years, surveys
demonstrated that this species was
found across the Bonneville Basin in
Utah, including Snake Valley. By the
1940s and 1950s, the numbers of least
chub in range and abundance surveys
were definitely decreasing with only 11
extant populations existing by 1979, and
3 extant wild populations known in
1995. UDWR surveys in the 1990s and
2000s discovered three new populations
on the eastern extent of the historic
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range; however, one of these
populations is functionally extirpated.
The Service now considers five extant,
wild, viable populations to exist, with
only three (all in Snake Valley) being
considered secure from the effects of
nonnative fish.
This status review found threats to the
least chub related to Factors A, C, D,
and E, as described in the following
paragraphs and summarized in Table 4.
We find that the best available
information for Factor A indicates that
listing the least chub as threatened or
endangered under the Act is warranted
due to the effects of livestock grazing
and water withdrawal and diversions on
the species and its habitat. Although the
LCCAS and the UDWR have worked to
protect least chub habitat with grazing
enclosures where possible and grazing
management plans in some areas,
livestock-grazing-related impacts are
still observed at most least chub sites.
There is substantial evidence showing
the negative effect of historical
groundwater withdrawal on least chub.
While uncertainty exists on the
magnitude of effects to the least chub
from proposed large-scale groundwater
pumping, concern regarding the
remaining five extant, wild populations
is sufficient to indicate that the species
is at risk of extinction in the foreseeable
future, especially when combined with
the threat of drought.
We find that the best available
information concerning Factor C
(Predation) indicates that listing the
least chub as threatened or endangered
under the Act is warranted due to the
continuing threat of nonnative species,
particularly mosquitofish, for which
there is no known means of control.
Several significant efforts have been
made to remove mosquitofish from least
chub habitats, without success. The
wild least chub population at Mona
Springs is functionally extirpated due to
mosquitofish, and nonnative fish are
present at two of the five remaining
viable populations.
We find that the best available
information concerning Factor D
(Inadequacy of Existing Regulatory
Mechanisms) indicates that the least
chub is at risk of extinction in the
foreseeable future due to inadequacy of
existing regulations to regulate
groundwater withdrawals and
ameliorate their effects on least chub
habitat.
We find that the best available
information concerning Factor E (Other
Natural or Manmade Factors Affecting
Its Continued Existence) indicates that
the least chub is at risk of extinction in
the foreseeable future because of the
cumulative effects of drought, current
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and climate change on the remaining
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naturally occurring populations in
Snake Valley.
TABLE 4.—SUMMARY OF LEAST CHUB STATUS AND THREATS BY POPULATION IN THE UNITED STATES.
Current
Status
Population
Current & Future Threats
Leland Harris Spring Complex
Extant
Gandy Salt Marsh
Extant
Bishop Springs Complex
Extant
Factor C. Nonnative fishes.
Mills Valley
Extant
Factor D. Inadequacy of existing mechanisms to regulate groundwater
withdrawal.
Factor E. Cumulative effects of climate change, groundwater withdrawal,
& drought.
Mona Springs
Extirpated
Clear Lake
Extant
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Because our finding on the petition to
list is warranted but precluded, we do
not need to specifically determine
whether it is appropriate to perform a
‘‘significant portion of the range’’
analysis for this species. Because of a
small and restricted population
distribution, and because of threats
described above, the least chub should
be listed as threatened or endangered
throughout its entire range. We will
review whether to list the species as
threatened or endangered during the
proposed listing rule process.
We have reviewed the available
information to determine if the existing
and foreseeable threats render the
species at risk of extinction now such
that issuing an emergency regulation
temporarily listing the species as per
section 4(b)(7) of the Act is warranted.
We have determined that issuing an
emergency regulation temporarily
listing the species is not warranted for
this species at this time because five
populations persist, three are currently
free from nonnative species, and all are
currently free from large-scale
groundwater pumping. However, if at
any time we determine that issuing an
emergency regulation temporarily
listing the least chub is warranted, we
will initiate this action at that time.
Preclusion and Expeditious Progress
Preclusion is a function of the listing
priority of a species in relation to the
resources that are available and
competing demands for those resources.
Thus, in any given fiscal year (FY),
multiple factors dictate whether it will
be possible to undertake work on a
proposed listing regulation or whether
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Factor A. Livestock grazing, groundwater withdrawal, drought.
Factor A. Groundwater withdrawal, drought.
Factor C. Nonnative fishes.
Factor D. Inadequacy of existing mechanisms to regulate groundwater
withdrawal.
Factor E. Cumulative effects of climate change, groundwater withdrawal,
& drought.
promulgation of such a proposal is
warranted but precluded by higherpriority listing actions.
The resources available for listing
actions are determined through the
annual Congressional appropriations
process. The appropriation for the
Listing Program is available to support
work involving the following listing
actions: Proposed and final listing rules;
90–day and 12–month findings on
petitions to add species to the Lists of
Endangered and Threatened Wildlife
and Plants (Lists) or to change the status
of a species from threatened to
endangered; annual determinations on
prior ‘‘warranted but precluded’’ petition
findings as required under section
4(b)(3)(C)(i) of the Act; critical habitat
petition findings; proposed and final
rules designating critical habitat; and
litigation-related, administrative, and
program-management functions
(including preparing and allocating
budgets, responding to Congressional
and public inquiries, and conducting
public outreach regarding listing and
critical habitat).
The work involved in preparing
various listing documents can be
extensive and may include, but is not
limited to: Gathering and assessing the
best scientific and commercial data
available and conducting analyses used
as the basis for our decisions; writing
and publishing documents; and
obtaining, reviewing, and evaluating
public comments and peer review
comments on proposed rules and
incorporating relevant information into
final rules. The number of listing
actions that we can undertake in a given
year also is influenced by the
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complexity of those listing actions; that
is, more complex actions generally are
more costly. For example, during the
past several years, the cost (excluding
publication costs) for preparing a 12–
month finding, without a proposed rule,
has ranged from approximately $11,000
for one species with a restricted range
and involving a relatively
uncomplicated analysis to $305,000 for
another species that is wide-ranging and
involving a complex analysis.
We cannot spend more than is
appropriated for the Listing Program
without violating the Anti-Deficiency
Act (see 31 U.S.C. 1341(a)(1)(A)). In
addition, in FY 1998 and for each fiscal
year since then, Congress has placed a
statutory cap on funds that may be
expended for the Listing Program, equal
to the amount expressly appropriated
for that purpose in that fiscal year. This
cap was designed to prevent funds
appropriated for other functions under
the Act (for example, recovery funds for
removing species from the Lists), or for
other Service programs, from being used
for Listing Program actions (see House
Report 105-163, 105th Congress, 1st
Session, July 1, 1997).
Recognizing that designation of
critical habitat for species already listed
would consume most of the overall
Listing Program appropriation, Congress
also put a critical habitat subcap in
place in FY 2002 and has retained it
each subsequent year to ensure that
some funds are available for other work
in the Listing Program: ‘‘The critical
habitat designation subcap will ensure
that some funding is available to
address other listing activities’’ (House
Report No. 107 - 103, 107th Congress, 1st
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Session, June 19, 2001). In FY 2002 and
each year until FY 2006, the Service has
had to use virtually the entire critical
habitat subcap to address courtmandated designations of critical
habitat, and consequently none of the
critical habitat subcap funds have been
available for other listing activities. In
FY 2007, we were able to use some of
the critical habitat subcap funds to fund
proposed listing determinations for
high-priority candidate species. In FY
2009, while we were unable to use any
of the critical habitat subcap funds to
fund proposed listing determinations,
we did use some of this money to fund
the critical habitat portion of some
proposed listing determinations so that
the proposed listing determination and
proposed critical habitat designation
could be combined into one rule,
thereby being more efficient in our
work. In FY 2010, we are using some of
the critical habitat subcap funds to fund
actions with statutory deadlines.
Thus, through the listing cap, the
critical habitat subcap, and the amount
of funds needed to address courtmandated critical habitat designations,
Congress and the courts have in effect
determined the amount of money
available for other listing activities.
Therefore, the funds in the listing cap,
other than those needed to address
court-mandated critical habitat for
already listed species, set the limits on
our determinations of preclusion and
expeditious progress.
Congress also recognized that the
availability of resources was the key
element in deciding, when making a 12–
month petition finding, whether we
would prepare and issue a listing
proposal or instead make a ‘‘warranted
but precluded’’ finding for a given
species. The Conference Report
accompanying Public Law 97-304,
which established the current statutory
deadlines and the warranted-butprecluded finding, states (in a
discussion on 90–day petition findings
that by its own terms also covers 12–
month findings) that the deadlines were
‘‘not intended to allow the Secretary to
delay commencing the rulemaking
process for any reason other than that
the existence of pending or imminent
proposals to list species subject to a
greater degree of threat would make
allocation of resources to such a petition
[that is, for a lower-ranking species]
unwise.’’
In FY 2010, expeditious progress is
that amount of work that can be
achieved with $10,471,000, which is the
amount of money that Congress
appropriated for the Listing Program
(that is, the portion of the Listing
Program funding not related to critical
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habitat designations for species that are
already listed). However these funds are
not enough to fully fund all our courtordered and statutory listing actions in
FY 2010, so we are using $1,114,417 of
our critical habitat subcap funds in
order to work on all of our required
petition findings and listing
determinations. This brings the total
amount of funds we have for listing
actions in FY 2010 to $11,585,417. Our
process is to make our determinations of
preclusion on a nationwide basis to
ensure that the species most in need of
listing will be addressed first and also
because we allocate our listing budget
on a nationwide basis. The $11,585,417
is being used to fund work in the
following categories: compliance with
court orders and court-approved
settlement agreements requiring that
petition findings or listing
determinations be completed by a
specific date; section 4 (of the Act)
listing actions with absolute statutory
deadlines; essential litigation-related,
administrative, and listing programmanagement functions; and highpriority listing actions for some of our
candidate species.
In 2009, the responsibility for listing
foreign species under the Act was
transferred from the Division of
Scientific Authority, International
Affairs Program, to the Endangered
Species Program. Starting in FY 2010, a
portion of our funding is being used to
work on the actions described above as
they apply to listing actions for foreign
species. This has the potential to further
reduce funding available for domestic
listing actions, although there are
currently no foreign species issues
included in our high-priority listing
actions at this time. The allocations for
each specific listing action are identified
in the Service’s FY 2010 Allocation
Table (part of our administrative
record).
In FY 2007, we had more than 120
species with an LPN of 2, based on our
September 21, 1983, guidance for
assigning an LPN for each candidate
species (48 FR 43098). Using this
guidance, we assign each candidate an
LPN of 1 to 12, depending on the
magnitude of threats (high vs. moderate
to low), immediacy of threats (imminent
or nonimminent), and taxonomic status
of the species (in order of priority:
monotypic genus (a species that is the
sole member of a genus); species; or part
of a species (subspecies, distinct
population segment, or significant
portion of the range)). The lower the
listing priority number, the higher the
listing priority (that is, a species with an
LPN of 1 would have the highest listing
priority). Because of the large number of
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high-priority species, we further ranked
the candidate species with an LPN of 2
by using the following extinction-risk
type criteria: International Union for the
Conservation of Nature and Natural
Resources (IUCN) Red list status/rank,
Heritage rank (provided by
NatureServe), Heritage threat rank
(provided by NatureServe), and species
currently with fewer than 50
individuals, or 4 or fewer populations.
Those species with the highest IUCN
rank (critically endangered), the highest
Heritage rank (G1), the highest Heritage
threat rank (substantial, imminent
threats), and currently with fewer than
50 individuals, or fewer than 4
populations, comprised a group of
approximately 40 candidate species
(‘‘Top 40’’). These 40 candidate species
have had the highest priority to receive
funding to work on a proposed listing
determination. As we work on proposed
and final listing rules for these 40
candidates, we are applying the ranking
criteria to the next group of candidates
with an LPN of 2 and 3 to determine the
next set of highest priority candidate
species.
To be more efficient in our listing
process, as we work on proposed rules
for these species in the next several
years, we are preparing multispecies
proposals when appropriate, and these
may include species with lower priority
if they overlap geographically or have
the same threats as a species with an
LPN of 2. In addition, available staff
resources are also a factor in
determining high-priority species
provided with funding. Finally,
proposed rules for reclassification of
threatened species to endangered are
lower priority, since as listed species,
they are already afforded the protection
of the Act and implementing
regulations.
We assign the least chub a Listing
Priority Number (LPN) of 7 based on our
finding that the species faces threats
that are of moderate magnitude and high
imminence. Under the Service’s LPN
Guidance (September 21, 1983; 48 FR
43098), the magnitude of threat is the
first criterion we look at when
establishing a listing priority. The
guidance indicates that species with the
highest magnitude of threat are those
species facing the greatest threats to
their continued existence. These species
receive the highest listing priority. At
present, the threats facing the least chub
do not meet the highest magnitude rank,
because the threats are not of uniform
intensity and the level of the threats is
moderate. Although many of the factors
we analyzed (e.g., grazing, groundwater
withdrawal, nonnative species) are
present throughout the range, they are
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not to the level that they are causing
high-magnitude threats to least chub in
the majority of the five remaining
populations. Grazing, groundwater
withdrawal, and nonnative predation
threats are of high magnitude in some
populations but are of low magnitude or
nonexistent in other populations, such
that when considering the overall
species’ range, the threats average out to
being of moderate magnitude.
Under our LPN Guidance, the second
criterion we consider in assigning a
listing priority is the immediacy of
threats. This criterion is intended to
ensure that the species facing actual,
identifiable threats are given priority
over those for which threats are only
potential or that are intrinsically
vulnerable but are not known to be
presently facing such threats. We
consider the threats imminent because
we have factual information that the
threats are identifiable and that the
species is currently facing them in many
portions of its range. These actual,
identifiable threats are covered in
greater detail in factors A and C of this
finding and include livestock grazing,
groundwater withdrawal, and nonnative
species predation.
The third criterion in our LPN
guidance is intended to devote
resources to those species representing
highly distinctive or isolated gene pools
as reflected by taxonomy. The least
chub is a species within a monotypic
genus, and therefore it receives a higher
priority than a species, subspecies, or
DPS.
We will continue to monitor the
threats to the least chub, and the
species’ status on an annual basis, and
should the magnitude or the imminence
of the threats change, we will revisit our
assessment of LPN.
Because we assigned the least chub an
LPN of 7, work on a proposed listing
determination for the least chub is
precluded by work on higher priority
listing actions with absolute statutory,
court ordered, or court-approved
deadlines and final listing
determinations for those species that
were proposed for listing with funds
from FY 2009. This work includes all
the actions listed in the tables below
under expeditious progress (see tables 5
and 6).
35419
As explained above, a determination
that listing is warranted but precluded
must also demonstrate that expeditious
progress is being made to add or remove
qualified species to and from the Lists
of Endangered and Threatened Wildlife
and Plants. (Although we do not discuss
it in detail here, we are also making
expeditious progress in removing
species from the Lists under the
Recovery program, which is funded by
a separate line item in the budget of the
Endangered Species Program. As
explained above in our description of
the statutory cap on Listing Program
funds, the Recovery Program funds and
actions supported by them cannot be
considered in determining expeditious
progress made in the Listing Program.)
As with our ‘‘precluded’’ finding,
expeditious progress in adding qualified
species to the Lists is a function of the
resources available and the competing
demands for those funds. Given that
limitation, we find that we are making
progress in FY 2010 in the Listing
Program. This progress included
preparing and publishing the following
determinations:
TABLE 5.—FY 2010 COMPLETED LISTING ACTIONS.
Publication
Date
Title
Actions
FR Pages
Listing Lepidium papilliferum (Slickspot Peppergrass) as a
Threatened Species Throughout Its Range
Final Listing Threatened
74 FR 52013-52064
10/27/2009
90-day Finding on a Petition To List the American Dipper in the
Black Hills of South Dakota as Threatened or Endangered
Notice of 90–day Petition Finding,
Not substantial
74 FR 55177-55180
10/28/2009
Status Review of Arctic Grayling (Thymallus arcticus) in the Upper
Missouri River System
Notice of Intent to Conduct
Status Review
74 FR 55524-55525
11/03/2009
Listing the British Columbia Distinct Population Segment of the
Queen Charlotte Goshawk Under the Endangered Species Act:
Proposed rule.
Proposed Listing Threatened
74 FR 56757-56770
11/03/2009
Listing the Salmon-Crested Cockatoo as Threatened Throughout
Its Range with Special Rule
Proposed Listing Threatened
74 FR 56770-56791
11/23/2009
Status Review of Gunnison sage-grouse (Centrocercus minimus)
Notice of Intent to Conduct
Status Review
74 FR 61100-61102
12/03/2009
12-Month Finding on a Petition to List the Black-tailed Prairie Dog
as Threatened or Endangered
Notice of 12–month petition
finding, Not warranted
74 FR 63343-63366
12/03/2009
90-Day Finding on a Petition to List Sprague’s Pipit as Threatened
or Endangered
Notice of 90–day Petition Finding,
Substantial
74 FR 63337-63343
12/15/2009
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10/08/2009
90-Day Finding on Petitions To List Nine Species of Mussels From
Texas as Threatened or Endangered With Critical Habitat
Notice of 90–day Petition Finding,
Substantial
74 FR 66260-66271
12/16/2009
Partial 90-Day Finding on a Petition to List 475 Species in the
Southwestern United States as Threatened or Endangered With
Critical Habitat
Notice of 90–day Petition Finding,
Not substantial and Subtantial
74 FR 66865-66905
12/17/2009
12–month Finding on a Petition To Change the Final Listing of the
Distinct Population Segment of the Canada Lynx To Include New
Mexico
Notice of 12–month petition
finding, Warranted but precluded
74 FR 66937-66950
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Federal Register / Vol. 75, No. 119 / Tuesday, June 22, 2010 / Proposed Rules
TABLE 5.—FY 2010 COMPLETED LISTING ACTIONS.—Continued
Publication
Date
Title
Actions
FR Pages
Listing Foreign Bird Species in Peru and Bolivia as Endangered
Throughout Their Range
Proposed Listing Endangered
75 FR 605-649
1/05/2010
Listing Six Foreign Birds as Endangered Throughout Their Range
Proposed Listing Endangered
75 FR 286-310
1/05/2010
Withdrawal of Proposed Rule to List Cook’s Petrel
Proposed rule, withdrawal
75 FR 310-316
1/05/2010
Final Rule to List the Galapagos Petrel and Heinroth’s Shearwater
as Threatened Throughout Their Ranges
Final Listing Threatened
75 FR 235-250
1/20/2010
Initiation of Status Review for Agave eggersiana and Solanum
conocarpum
Notice of Intent to Conduct
Status Review
75 FR 3190-3191
2/09/2010
12–month Finding on a Petition to List the American Pika as
Threatened or Endangered
Notice of 12–month petition
finding, Not warranted
75 FR 6437-6471
2/25/2010
12-Month Finding on a Petition To List the Sonoran Desert Population of the Bald Eagle as a Threatened or Endangered Distinct
Population Segment
Notice of 12–month petition finding, Not warranted
75 FR 8601-8621
2/25/2010
Withdrawal of Proposed Rule To List the Southwestern Washington/Columbia River Distinct Population Segment of Coastal
Cutthroat Trout (Oncorhynchus clarki clarki) as Threatened
Withdrawal of Proposed Rule to
List
75 FR 8621-8644
3/18/2010
90-Day Finding on a Petition to List the Berry Cave salamander as
Endangered
Notice of 90–day Petition Finding,
Substantial
75 FR 13068-13071
3/23/2010
90-Day Finding on a Petition to List the Southern Hickorynut Mussel (Obovaria jacksoniana) as Endangered or Threatened
Notice of 90–day Petition Finding,
Not substantial
75 FR 13717-13720
3/23/2010
90-Day Finding on a Petition to List the Striped Newt as Threatened
Notice of 90–day Petition Finding,
Substantial
75 FR 13720-13726
3/23/2010
12-Month Findings for Petitions to List the Greater Sage-Grouse
(Centrocercus urophasianus)as Threatened or Endangered
Notice of 12–month petition finding, Warranted but precluded
75 FR 13910-14014
3/31/2010
12-Month Finding on a Petition to List the Tucson Shovel-Nosed
Snake (Chionactis occipitalis klauberi) as Threatened or Endangered with Critical Habitat
Notice of 12–month petition finding, Warranted but precluded
75 FR 16050-16065
4/5/2010
90-Day Finding on a Petition To List Thorne’s Hairstreak Butterfly
as or Endangered
Notice of 90–day Petition Finding,
Substantial
75 FR 17062-17070
4/6/2010
12–month Finding on a Petition To List the Mountain Whitefish in
the Big Lost River, Idaho, as Endangered or Threatened
Notice of 12–month petition finding, Not warranted
75 FR 17352-17363
4/6/2010
90-Day Finding on a Petition to List a Stonefly (Isoperla jewetti)
and a Mayfly (Fallceon eatoni) as Threatened or Endangered
with Critical Habitat
Notice of 90–day Petition Finding,
Not substantial
75 FR 17363-17367
4/7/2010
12-Month Finding on a Petition to Reclassify the Delta Smelt From
Threatened to Endangered Throughout Its Range
Notice of 12–month petition finding, Warranted but precluded
75 FR 17667-17680
4/13/2010
Determination of Endangered Status for 48 Species on Kauai and
Designation of Critical Habitat
Final Listing Endangered
75 FR 18959-19165
4/15/2010
Initiation of Status Review of the North American Wolverine in the
Contiguous United States
Notice of Initiation of Status Review
75 FR 19591-19592
4/15/2010
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1/05/2010
12-Month Finding on a Petition to List the Wyoming Pocket Gopher
as Endangered or Threatened with Critical Habitat
Notice of 12–month petition finding, Not warranted
75 FR 19592-19607
4/16/2010
90-Day Finding on a Petition to List a Distinct Population Segment
of the Fisher in Its United States Northern Rocky Mountain
Range as Endangered or Threatened with Critical Habitat
Notice of 90–day Petition Finding,
Substantial
75 FR 19925-19935
4/20/2010
Initiation of Status Review for Sacramento splittail (Pogonichthys
macrolepidotus)
Notice of Initiation of Status Review
75 FR 20547-20548
4/26/2010
90-Day Finding on a Petition to List the Harlequin Butterfly as Endangered
Notice of 90–day Petition Finding,
Substantial
75 FR 21568-21571
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Federal Register / Vol. 75, No. 119 / Tuesday, June 22, 2010 / Proposed Rules
TABLE 5.—FY 2010 COMPLETED LISTING ACTIONS.—Continued
Publication
Date
Title
Actions
FR Pages
4/27/2010
12-Month Finding on a Petition to List Susan’s Purse-making
Caddisfly (Ochrotrichia susanae) as Threatened or Endangered
Notice of 12–month petition finding, Not warranted
75 FR 22012-22025
4/27/2010
90–day Finding on a Petition to List the Mohave Ground Squirrel
as Endangered with Critical Habitat
Notice of 90–day Petition Finding,
Substantial
75 FR 22063-22070
5/4/2010
90-Day Finding on a Petition to List Hermes Copper Butterfly as
Threatened or Endangered
Notice of 90–day Petition Finding,
Substantial
75 FR 23654-23663
Our expeditious progress also
includes work on listing actions that we
funded in FY 2010 but have not yet
been completed to date. These actions
are listed below. Actions in the top
section of the table are being conducted
under a deadline set by a court. Actions
in the middle section of the table are
being conducted to meet statutory
timelines, that is, timelines required
under the Act. Actions in the bottom
section of the table are high-priority
listing actions. These actions include
work primarily on species with an LPN
of 2, and selection of these species is
partially based on available staff
resources, and when appropriate,
include species with a lower priority if
they overlap geographically or have the
same threats as the species with the
high priority. Including these species
together in the same proposed rule
results in considerable savings in time
and funding, as compared to preparing
separate proposed rules for each of them
in the future.
TABLE 6.—ACTIONS FUNDED IN FY 2010 BUT NOT YET COMPLETED.
Species
Action
Actions Subject to Court Order/Settlement Agreement
6 Birds from Eurasia
Final listing determination
Flat-tailed horned lizard
Final listing determination
Mountain plover
Final listing determination
6 Birds from Peru
Proposed listing determination
Sacramento splittail
Proposed listing determination
White-tailed prairie dog
12–month petition finding
Gunnison sage-grouse
12–month petition finding
Wolverine
12–month petition finding
Arctic grayling
12–month petition finding
Agave eggergsiana
12–month petition finding
Solanum conocarpum
12–month petition finding
Mountain plover
12–month petition finding
Thorne’s Hairstreak Butterfly
12–month petition finding
Hermes copper butterfly
12–month petition finding
Actions with Statutory Deadlines
Final listing determination
Georgia pigtoe, interrupted rocksnail, and rough hornsnail
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Casey’s june beetle
Final listing determination
2 Hawaiian damselflies
Final listing determination
African penguin
Final listing determination
3 Foreign bird species (Andean flamingo, Chilean woodstar, St. Lucia forest thrush)
Final listing determination
5 Penguin species
Final listing determination
Southern rockhopper penguin – Campbell Plateau population
Final listing determination
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Federal Register / Vol. 75, No. 119 / Tuesday, June 22, 2010 / Proposed Rules
TABLE 6.—ACTIONS FUNDED IN FY 2010 BUT NOT YET COMPLETED.—Continued
Species
Action
5 Bird species from Colombia and Ecuador
Final listing determination
7 Bird species from Brazil
Final listing determination
Queen Charlotte goshawk
Final listing determination
Salmon crested cockatoo
Proposed listing determination
Black-footed albatross
12–month petition finding
Mount Charleston blue butterfly
12–month petition finding
Least chub1
12–month petition finding
Mojave fringe-toed lizard1
12–month petition finding
Pygmy rabbit (rangewide)1
12–month petition finding
Kokanee – Lake Sammamish population1
12–month petition finding
Delta smelt (uplisting)
12–month petition finding
Cactus ferruginous
pygmy-owl1
12–month petition finding
Northern leopard frog
12–month petition finding
Tehachapi slender salamander
12–month petition finding
Coqui Llanero
12–month petition finding
White-sided jackrabbit
12–month petition finding
Jemez Mountains salamander
12–month petition finding
Dusky tree vole
12–month petition finding
Eagle Lake trout1
12–month petition finding
29 of 206 species
12–month petition finding
Desert tortoise – Sonoran population
12–month petition finding
Gopher tortoise – eastern population
12–month petition finding
Amargosa toad
12–month petition finding
Pacific walrus
12–month petition finding
Wrights marsh thistle
12–month petition finding
67 of 475 southwest species
12–month petition finding
9 Southwest mussel species
12–month petition finding
14 parrots (foreign species)
12–month petition finding
Berry Cave salamander1
12–month petition finding
Striped
Newt1
12–month petition finding
12–month petition finding
Mohave Ground Squirrel1
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Fisher – Northern Rocky Mountain Range1
12–month petition finding
Puerto Rico Harlequin Butterfly
12–month petition finding
Southeastern pop snowy plover & wintering pop. of piping plover1
90–day petition finding
Eagle Lake trout1
90–day petition finding
Ozark chinquapin1
90–day petition finding
Smooth-billed ani1
90–day petition finding
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Federal Register / Vol. 75, No. 119 / Tuesday, June 22, 2010 / Proposed Rules
TABLE 6.—ACTIONS FUNDED IN FY 2010 BUT NOT YET COMPLETED.—Continued
Species
Action
Bay Springs salamander1
32 species of snails and
90–day petition finding
slugs1
90–day petition finding
Calopogon oklahomensis1
90–day petition finding
White-bark pine
90–day petition finding
42 snail species (Nevada & Utah)
90–day petition finding
HI yellow-faced bees
90–day petition finding
Red knot roselaari subspecies
90–day petition finding
Honduran emerald
90–day petition finding
Peary caribou
90–day petition finding
Western gull-billed tern
90–day petition finding
Plain bison
90–day petition finding
Giant Palouse earthworm
90–day petition finding
Mexican gray wolf
90–day petition finding
Spring Mountains checkerspot butterfly
90–day petition finding
Spring pygmy sunfish
90–day petition finding
San Francisco manzanita
90–day petition finding
Bay skipper
90–day petition finding
Unsilvered fritillary
90–day petition finding
Texas kangaroo rat
90–day petition finding
Spot-tailed earless lizard
90–day petition finding
Eastern small-footed bat
90–day petition finding
Northern long-eared bat
90–day petition finding
Prairie chub
90–day petition finding
10 species of Great Basin butterfly
90–day petition finding
6 sand dune (scarab) beetles
90–day petition finding
Gila monster – Utah population
90–day petition finding
Golden-winged warbler
90–day petition finding
Sand-verbena moth
90–day petition finding
Aztec (beautiful) gilia
90–day petition finding
Arapahoe snowfly
90–day petition finding
High Priority Listing Actions3
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19 Oahu candidate species3 (16 plants, 3 damselflies) (15 with LPN = 2, 3 with LPN = 3, 1 with LPN =9)
17 Maui-Nui candidate
species3
(14 plants, 3 tree snails) (12 with LPN = 2, 2 with LPN = 3, 3 with LPN = 8)
Proposed listing
Proposed listing
Sand dune lizard3 (LPN = 2)
Proposed listing
2 Arizona springsnails3 (Pyrgulopsis bernadina (LPN = 2), Pyrgulopsis trivialis (LPN = 2))
Proposed listing
2 New Mexico springsnails3 (Pyrgulopsis chupaderae (LPN = 2), Pyrgulopsis thermalis (LPN = 11))
Proposed listing
2 mussels3 (rayed bean (LPN = 2), snuffbox No LPN)
Proposed listing
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Federal Register / Vol. 75, No. 119 / Tuesday, June 22, 2010 / Proposed Rules
TABLE 6.—ACTIONS FUNDED IN FY 2010 BUT NOT YET COMPLETED.—Continued
Species
Action
2 mussels3 (sheepnose (LPN = 2), spectaclecase (LPN = 4),)
Ozark
hellbender2
Proposed listing
(LPN = 3)
Proposed listing
Altamaha spinymussel3 (LPN = 2)
Proposed listing
5 southeast fish3 (rush darter (LPN = 2), chucky madtom (LPN = 2), yellowcheek darter (LPN = 2),
Cumberland darter (LPN = 5), laurel dace (LPN = 5))
Proposed listing
8 southeast mussels (southern kidneyshell (LPN = 2), round ebonyshell (LPN = 2), Alabama pearlshell (LPN
= 2), southern sandshell (LPN = 5), fuzzy pigtoe (LPN = 5), Choctaw bean (LPN = 5), narrow pigtoe (LPN
= 5), and tapered pigtoe (LPN = 11))
Proposed listing
3 Colorado plants3 (Pagosa skyrocket (Ipomopsis polyantha) (LPN = 2), Parchute beardtongue (Penstemon
debilis) (LPN = 2), Debeque phacelia (Phacelia submutica) (LPN = 8))
Proposed listing
1
Funds for listing actions for these species were provided in previous FYs.
We funded a proposed rule for this subspecies with an LPN of 3 ahead of other species with LPN of 2, because the threats to the species
were so imminent and of a high magnitude that we considered emergency listing if we were unable to fund work on a proposed listing rule in FY
2008.
3 Funds for these high-priority listing actions were provided in FY 2008 or 2009.
2
We have endeavored to make our
listing actions as efficient and timely as
possible, given the requirements of the
relevant law and regulations, and
constraints relating to workload and
personnel. We are continually
considering ways to streamline
processes or achieve economies of scale,
such as by batching related actions
together. Given our limited budget for
implementing section 4 of the Act, these
actions described above collectively
constitute expeditious progress.
The least chub will be added to the
list of candidate species upon
publication of this 12–month finding.
We will continue to monitor the status
of this species as new information
becomes available. This review will
determine if a change in status is
warranted, including the need to make
prompt use of emergency listing
procedures.
We intend that any proposed listing
action for the least chub will be as
accurate as possible. Therefore, we will
continue to accept additional
information and comments from all
concerned governmental agencies, the
scientific community, industry, or any
other interested party concerning this
finding.
srobinson on DSKHWCL6B1PROD with PROPOSALS
References Cited
A complete list of references cited is
available on the Internet at https://
www.regulations.gov and upon request
from the Utah Field Office (see
ADDRESSES section).
Authors
The primary authors of this notice are
the staff members of the Utah Field
Office.
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Authority
The authority for this action is section
4 of the Endangered Species Act of
1973, as amended (16 U.S.C. 1531 et
seq.).
Dated: June 4, 2010
Jeffrey L. Underwood
Acting Director, U.S. Fish and Wildlife Service
[FR Doc. 2010–15070 Filed 6–21–10; 8:45 am]
BILLING CODE 4310–55–S
DEPARTMENT OF THE INTERIOR
Fish and Wildlife Service
50 CFR Part 17
[FWS–R4–ES–2008–0119; 92220–1113–
0000–C6]
RIN 1018–AX01
Endangered and Threatened Wildlife
and Plants; Proposed Reclassification
of the Tulotoma Snail From
Endangered to Threatened
AGENCY: Fish and Wildlife Service,
Interior.
ACTION: Proposed rule.
SUMMARY: We, the U.S. Fish and
Wildlife Service (Service), propose to
reclassify the tulotoma snail (Tulotoma
magnifica) from endangered to
threatened, under the authority of the
Endangered Species Act of 1973, as
amended (Act). This proposed action is
based on a review of the best available
scientific and commercial data, which
indicate that the endangered
designation no longer correctly reflects
the status of this snail. We have
documented a substantial improvement
in the species’ distribution and numbers
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over the past 15 years, including the
discovery of several populations that
were unknown when the species was
listed. Minimum flows and other
conservation measures have been
implemented below two dams in the
Coosa River, improving habitat and
resulting in the expansion of tulotoma
snail numbers and range in the Coosa
River. The Alabama Clean Water
Partnership has also developed the
Lower Coosa River Basin Management
Plan to address nonpoint source
pollution and watershed management
issues in most Coosa River tributaries
occupied by the tulotoma snail. While
great strides have been made to improve
the species status, additional efforts are
required to address the remaining
threats to the species. We are seeking
comments from the public on this
proposal.
DATES: We will accept comments
received or postmarked on or before
August 23, 2010. We must receive
requests for public hearings, in writing,
at the address shown in the FOR FURTHER
INFORMATION CONTACT section by August
6, 2010.
ADDRESSES: You may submit comments
by one of the following methods:
• Federal eRulemaking Portal: https://
www.regulations.gov. Follow the
instructions for submitting comments
on Docket No. FWS–R4–ES–2008–0119.
• U.S. mail or hand-delivery: Public
Comments Processing, Attn: RIN 1018–
AW08; Division of Policy and Directives
Management; U.S. Fish and Wildlife
Service; 4401 N. Drive, Suite 222;
Arlington, VA 22203.
We will not accept e-mail or faxes. We
will post all comments on https://
www.regulations.gov. This generally
E:\FR\FM\22JNP1.SGM
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Agencies
[Federal Register Volume 75, Number 119 (Tuesday, June 22, 2010)]
[Proposed Rules]
[Pages 35398-35424]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2010-15070]
[[Page 35398]]
-----------------------------------------------------------------------
DEPARTMENT OF THE INTERIOR
Fish and Wildlife Service
50 CFR Part 17
[Docket No. FWS-R6-ES-2008-0088]
[MO 92210-0-0008-B2]
Endangered and Threatened Wildlife and Plants; 12-Month Finding
on a Petition to List the Least Chub as Threatened or Endangered
AGENCY: Fish and Wildlife Service, Interior.
ACTION: Notice of 12-month petition finding.
-----------------------------------------------------------------------
SUMMARY: We, the U.S. Fish and Wildlife Service (Service), announce a
12-month finding on a petition to list the least chub (Iotichthys
phlegethontis), a fish, as threatened or endangered and to designate
critical habitat under the Endangered Species Act of 1973, as amended
(Act). After review of all available scientific and commercial
information, we find that listing the least chub as threatened or
endangered under the Act is warranted. Currently, however, listing the
least chub is precluded by higher priority actions to amend the Lists
of Endangered and Threatened Wildlife and Plants. Upon publication of
this 12-month petition finding, we will add the least chub to our list
of candidate species with a listing priority number (LPN) of 7. We will
develop a proposed rule to list this species as our priorities and
funding allow. We will make any determination on critical habitat
during development of the proposed listing rule. In the interim, we
will address the status of the candidate taxon through our annual
Candidate Notice of Review (CNOR).
DATES: This finding was made on June 22, 2010.
ADDRESSES: This finding is available on the Internet at https://www.regulations.gov at Docket Number FWS-R6-ES-2008-0088 and https://www.fws.gov/mountain-prairie/species/fish/leastchub. 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 Field Office, 2369
West Orton Circle, Suite 50, West Valley City, UT 84119. Please submit
any new information, materials, comments, or questions concerning this
finding to the above address.
FOR FURTHER INFORMATION CONTACT: Larry Crist, Field Supervisor, U.S.
Fish and Wildlife Service, Utah Ecological Services Field Office (see
ADDRESSES); by telephone at (801) 975-3330; or by facsimile at (801)
975-3331. Persons who use a telecommunications device for the deaf
(TDD) may call the Federal Information Relay Service (FIRS) at 800-877-
8339.
SUPPLEMENTARY INFORMATION:
Background
Section 4(b)(3)(B) of the Act (16 U.S.C. 1531 et seq.), requires
that, for any petition to revise the Federal Lists of Threatened and
Endangered Wildlife and Plants that contains substantial scientific or
commercial information indicating that listing the species may be
warranted, we make a finding within 12 months of the date of receipt of
the petition. In this finding, we determine that the petitioned action
is: (a) Not warranted, (b) warranted, or (c) warranted, but 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 Federal Lists of Endangered and
Threatened Wildlife and Plants. Section 4(b)(3)(C) of the Act requires
that we treat a petition for which the requested action is found to be
warranted but precluded as though resubmitted on the date of such
finding, that is, requiring a subsequent finding to be made within 12
months. We must publish these 12-month findings in the Federal
Register.
Previous Federal Actions
In 1980, the Service reviewed the status of the least chub and
determined that there was insufficient data to warrant its listing as
an endangered or threatened species under the Act. On December 30,
1982, we classified the least chub as a Category 2 Candidate Species
(47 FR 58454). Category 2 included taxa for which information in the
Service's possession indicated that a proposed listing rule was
possibly appropriate, but for which sufficient data on biological
vulnerability and threats were not available to support a proposed
rule. In 1989, we conducted a new status review, and reclassified the
least chub as a Category 1 Candidate Species (54 FR 554). Category 1
included taxa for which the Service had substantial information in our
possession on biological vulnerability and threats to support
preparation of listing proposals. The Service ceased using category
designations in February 1996. On September 29, 1995, we published a
proposed rule to list the least chub as endangered with critical
habitat (60 FR 50518). A listing moratorium, imposed by Congress in
1995, suspended all listing activities and further action on the
proposal was postponed.
During the moratorium, the Service, Utah Division of Wildlife
Resources (UDWR), Bureau of Land Management (BLM), Bureau of
Reclamation (BOR), Utah Reclamation Mitigation and Conservation
Commission (URMCC), Confederated Tribes of the Goshute Reservation, and
Central Utah Water Conservancy District (CUWCD) developed a Least Chub
Conservation Agreement and Strategy (LCCAS), and formed the Least Chub
Conservation Team (LCCT) (Perkins et al. 1998, entire). The goals of
the LCCAS are to ensure the species' long-term survival within its
historic range and to assist in the development of rangewide
conservation efforts. The objectives of the LCCAS are to eliminate or
significantly reduce threats to the least chub and its habitat, to the
greatest extent possible, and to ensure the continued existence of the
species by restoring and maintaining a minimum number of least chub
populations throughout its historic range. The LCCT implements the
LCCAS and monitors populations, threats, and habitat conditions. The
LCCAS was updated and revised in 2005 (Bailey et al. 2005, entire).
As a result of conservation actions and commitments made by
signatories to the 1998 LCCAS (Perkins et al. 1998, p. 10), measures to
protect the least chub were developed and implemented. Consequently, we
withdrew the listing proposal on July 29, 1999 (64 FR 41061).
On June 25, 2007, we received a petition dated June 19, 2007, from
Center for Biological Diversity, Confederated Tribes of the Goshute
Reservation, Great Basin Chapter of Trout Unlimited, and Utah Chapter
of the Sierra Club requesting that the least chub be listed as
threatened under the Act and critical habitat be designated. Included
in the petition and supplement was supporting information regarding the
species' taxonomy and ecology, historical and current distribution,
present status, and actual and potential causes of decline. We
acknowledged the receipt of the petition and supplement in a letter to
Center for Biological Diversity, Confederated Tribes of the Goshute
Reservation, Great Basin Chapter of Trout Unlimited, and Utah Chapter
of the Sierra Club, dated July 13, 2007. In that letter, we also stated
that because of staff and budget limitations, it was not practical for
us to begin processing the petition at that time. Based on the
population status and alleged threats described in the
[[Page 35399]]
petition, we found no compelling evidence to support an emergency
listing at that time.
Funding became available to begin work on the 90-day finding in
Fiscal Year (FY) 2008. On October 15, 2008, we published a 90-day
finding that the petitioners provided substantial information
indicating that the species may be warranted for listing under the Act,
initiated the 12-month finding, and opened a 60-day public comment
period (73 FR 61007). This notice constitutes the 12-month finding on
the June 19, 2007, petition to list the least chub as threatened or
endangered.
Species Information
Taxonomy and Species Description
The least chub (Iotichthys phlegethontis) is an endemic minnow
(Family Cyprinidae) of the Bonneville Basin in Utah. Historically,
ancient lakes Bonneville and Provo largely covered the Bonneville
Basin, but over the past 16,000 years (since the Pleistocene period),
these lakes receded, leaving behind the current hydrology of the area
(Currey et al. 1984, p. 1). Least chub likely persisted in peripheral
freshwater sources to the receding lakes and were widely distributed in
a variety of the resulting habitat types, including rivers, streams,
springs, ponds, marshes, and swamps (Sigler and Miller 1963, p. 91).
The species' taxonomic classification has evolved over time, as
described in the 1995 proposed rule (60 FR 50518). The least chub is
currently classified within the monotypic genus (containing only one
species) Iotichthys (Jordan et al. 1930, in Hickman 1989, p. 16; Robins
et al. 1991, p. 21).
As implied by its common name, the least chub is a small fish less
than 55 millimeters (2.1 inches) long, identified by an upturned or
oblique mouth, large scales, and the absence of an incomplete lateral
line (rarely with one or two pored scales) (Sigler and Sigler 1987, p.
182). It has a deeply compressed body, with the front-most part of the
dorsal fin (on the back) lying behind the insertion of the pelvic fin
(on the underside of the body), and a slender caudle peduncle (area
connecting tail fin to the body) (Sigler and Miller 1963, p. 83).
Dorsal fin rays number eight (rarely nine), and anal fin rays also
number eight (Sigler and Miller 1963, p. 83). The pharyngeal teeth
(located near the pharynx) are in two rows (Sigler and Miller 1963, p.
83).
The least chub is a colorful species. Individuals have a gold
stripe along blue sides with white to yellow fins (Sigler and Sigler
1987, p. 182). Spawning males are olive-green above, steel-blue on the
sides, and have a golden stripe behind the upper end of the gill
opening (Sigler and Sigler 1987, p. 182). The fins are lemon-amber, and
sometimes the paired fins are bright golden-amber (Sigler and Sigler
1987, p. 182). Females and young are pale olive above, silvery on the
sides, and have watery-white fins; their eyes are silvery, with a
little gold coloration (Sigler and Sigler 1987, p. 182).
Life History
Sigler and Sigler (1987, p. 183) considered the least chub to be a
slow-growing species that rarely lives beyond 3 years of age. However,
least chub in natural systems live longer than originally thought (some
least chub may live to be 6 years of age) and growth rates vary among
populations (Mills et al. 2004a, p. 409). Differences in growth rates
may result from a variety of interacting processes, including food
availability, genetically based traits, population density, and water
temperatures (Mills et al. 2004a, p. 411).
Least chub are opportunistic feeders, and their diets reflect
availability and abundance of food items in different seasons and
habitat types (Crist and Holden 1980, p. 808; Lamarra 1981, p. 5;
Workman et al. 1979, p. 23). Although least chub diets change
throughout the year, they regularly consume algae (Chlorophyta and
Chrysophyta), midges (Chironomidae), microcrustaceans, copepods,
ostracods, and diatomaceous material (Sigler and Sigler 1987, p. 183).
Maintaining hydrologic connections between springheads and marsh
areas is important in fulfilling the least chub's ecological
requirements (Crawford 1979, p. 63; Crist and Holden 1980, p. 804;
Lamarra 1981, p. 10). Least chub follow thermal patterns for habitat
use. In April and May, they use the flooded, warmer, vegetated marsh
areas at water temperatures of about 16 [deg]C (60 [deg]F) (Crawford
1979, pp. 59, 74), but in late summer and fall they retreat to spring
heads as the water recedes, to overwinter (Crawford 1979, p. 58). In
the spring, the timing of spawning is a function of temperature and
photoperiod (Crawford 1979, p. 39).
The least chub is a partial and intermittent spawner, and spawns
within aquatic vegetation (Crawford 1979, p. 74). Adhesive eggs attach
to the emergent plants that provide the eggs, larvae, and young with
oxygen, food, and cover (Crist and Holden 1980, p. 808). Females
release only a few eggs at a time, but continue spawning for an
extended period. Total numbers of eggs produced are an indication of
fecundity, and individual females produce from 300 to 2,700 eggs
(Crawford 1979, p. 62). Fertilized eggs hatch in approximately 2 days
at a water temperature of 22 [deg]C (72 [deg]F) (Crawford 1979, p. 74).
Although peak spawning activity occurs in May, the reproductive season
lasts from April to August, and sometimes longer, depending on
environmental conditions such as photoperiod and water temperature
(Crawford 1979, pp. 47-48). This reproductive strategy (i.e.,
repetitive spawning over a period of many weeks) allows the least chub
to persist in fluctuating environmental conditions typical of desert
habitats (Crawford 1978, p. 2).
Larval least chub grow larger and young fry survive better in silt
substrate habitats (Wagner et al. 2006, pp. 1, 4, 7). The maximum
growth rate for least chub less than 1 year of age occurs at 22.3
[deg]C (72 [deg]F) under captive conditions (Billman et al. 2006, p.
434). Thermal preferences demonstrate the importance of warm rearing
habitats in producing strong year classes and viable populations
(Billman et al. 2006, p. 434).
Distribution
The first documented collection of least chub is from a ``brook''
near Salt Lake City in 1871 (Hickman 1989, p. 16). Between 1871 and
1979, many least chub occurrences were reported across the State,
ranging from the eastern portions of the Snake Valley to the Wasatch
Front and from the northern extent of the Bear River south to the
Beaver River (table 1). Least chub were very common in tributaries to
the Sevier, Utah, and Great Salt Lakes in the beginning of the 20th
Century (Jordan 1891, p. 30; Jordan and Evermann 1896, in Hickman 1989,
p. 1).
Table 1.--Summary of historic collections of least chub.
----------------------------------------------------------------------------------------------------------------
GEOGRAPH AREA Location Year Collected Reference
----------------------------------------------------------------------------------------------------------------
Wasatch Front Northwest Salt Lake 1933 Hickman 1989, pp. 16-17
City
----------------------------------------------------------------------------------------------------------------
qdrt;;
[[Page 35400]]
Big Cottonwood Creek 1953 Sigler & Miller 1963,
pp. 82-83
----------------------------------------------------------------------------------------------------------------
qdrt;;Davis County (2 1964 Hickman 1989, pp. 16-
miles west of 17; Bailey et al.
Centerville) 2005, p. 16
----------------------------------------------------------------------------------------------------------------
qdrt;;Farmington Bay 1965 Hickman 1989, pp. 16-
17; Bailey et al.
2005, p. 16
----------------------------------------------------------------------------------------------------------------
qdrt;;Provo River 1891 Jordan 1891, p. 30
----------------------------------------------------------------------------------------------------------------
qdrt;;Provo River (at 1931 & 1936 Tanner 1936, p. 170
confluence with Utah
Lake)
======================================
Northern Bear River 1894 Thompson 2008, p. 1
======================================
Southern Beaver River 1875 Cope & Yarrow 1875, pp.
656-657
----------------------------------------------------------------------------------------------------------------
qdrt;;Beaver River; 1942 Hubbs et al. 1942, in
Parowan Creek; Clear Sigler & Miller 1963,
Creek; & Little Salt p. 82
Lake
----------------------------------------------------------------------------------------------------------------
qdrt;;Sevier Lake 1896 Jordan & Evermann 1896,
in Bailey et al. 2005,
p. 16
======================================
Snake Valley Chimneys Spring; Big 1942 Hickman 1989, p. 16-17
Spring; Foote Ranch;
Small Knoll; & Gandy
area
----------------------------------------------------------------------------------------------------------------
qdrt;;Leland Harris 1970 Hickman 1989, p. 16
Spring Complex & Gandy
Salt Marsh
----------------------------------------------------------------------------------------------------------------
qdrt;;Leland Harris 1979 Workman et al. 1979,
Spring Complex; Bishop pp. 157-159
Spring Complex (Foote
Reservoir & Twin
Spring); & Gandy
Spring Complex
----------------------------------------------------------------------------------------------------------------
qdrt;;Callao, Utah 1979 Workman et al. 1979,
(Bagley Ranch & Redden pp. 157-159
Spring)
----------------------------------------------------------------------------------------------------------------
By the 1940s and 1950s, the numbers of least chub were decreasing
(Holden 1974, in Hickman 1989, p. 2). Only 11 known populations existed
by 1979 (Workman et al. 1979, pp. 156-158). By 1989, least chub had not
been collected outside of the Snake Valley for the previous 25 years
(Hickman 1989, p. 2). Three wild least chub populations were extant in
1995 (60 FR 50518) (Leland Harris Spring Complex, Gandy Salt Marsh,
Bishop Spring Complex).
The current distribution of the least chub is highly reduced from
its historic range. The UDWR began surveying for new populations and
monitoring existing populations Statewide in 1993. As a result, UDWR
found three previously unknown populations of least chub: Mona Springs
in 1995, Mills Valley in 1998, and Clear Lake in 2003 (Mock and Miller
2003, p. 3; Hines et al. 2008, pp. 44-45). The Mona Springs site is in
the southeastern portion of the Great Salt Lake subbasin and occurs on
the eastern border of ancient Lake Bonneville, near the highly
urbanized Wasatch Front. Clear Lake and Mills Valley are both in the
Sevier subbasin, in relatively undeveloped sites (Hines et al. 2008, p.
17). A comparison of survey results from the 1970s (Workman et al.
1979, pp. 156-158) to surveys from 1993 to 2007 (Hines et al. 2008, pp.
36-45) indicates that a majority of the natural populations extant in
1979 were extirpated by 2007 (table 2).
Table 2.--Comparison of least chub collections in 1979 and their
updated status in 2007.
Asterisk (*) denotes populations discovered after 1979.
Status categories:
Stable = viable self-sustaining population
Functionally extirpated = a limited number of least chub
present but population is not self sustaining
Extirpated = least chub no longer present at that location
Secure = no immediate threats present
Not secure = immediate threat(s) present
------------------------------------------------------------------------
1979 Population Status in 2007
------------------------------------------------------------------------
Leland Harris Spring Complex Stable - Secure
===========================================
Gandy Salt Marsh Stable - Secure
===========================================
Bishop Springs Stable - Secure
===========================================
Mills Valley* Stable - Not secure
===========================================
Clear Lake Wildlife Management Area* Stable - Not secure
===========================================
Mona Springs* Functionally
extirpated
===========================================
Redden Springs Extirpated
===========================================
Bagley Ranch Complex Extirpated
===========================================
Knoll Spring (not verified) Extirpated
===========================================
Cecil Garland Ranch Extirpated
===========================================
Tie House Extirpated
===========================================
Donner Extirpated
===========================================
Cold Extirpated
------------------------------------------------------------------------
Five wild, extant populations of least chub remain: the Leland
Harris Spring Complex, Gandy Salt Marsh, Bishop Springs Complex, Mills
Valley, and Clear Lake (Hines et al. 2008, pp. 34-45). Three of these
populations (the Leland Harris Spring Complex, Gandy Salt Marsh, and
Bishop Spring Complex) occur in the Snake Valley of Utah's west desert
and are genetically similar and very close in proximity to
[[Page 35401]]
each other (Mock and Miller 2003, pp. 17-18). The two remaining extant
populations (Mills Valley and Clear Lake) are located on the
southeastern border of the native range.
Least chub are still found in small numbers at the Mona Springs
site (Hines et al. 2008, p. 37). However, because this small number of
least chub does not compose a viable self-sustaining population (LCCT
2008a, p. 3), we consider the least chub population at Mona Springs
functionally extirpated (see discussion below). The Snake Valley, Mills
Valley, Clear Lake, and Mona Springs populations are each genetically
distinct (Mock and Miller 2005, p. 276; Mock and Bjerregaard 2007, p.
146). A brief description of the extant wild and the Mona Springs least
chub populations is found below.
(1) Leland Harris Spring Complex: R.R. Miller first collected least
chub at this site, located north of the Juab/Millard County line, in
1970 (Sigler and Sigler 1987, p. 182). The site consists of 12 to 15
springheads that feed a playa wetland with habitat fluctuating in size
seasonally. Least chub have had a persistent presence since monitoring
began by the UDWR in 1993 (Hines et al. 2008, pp. 41-43). Another
spring in the area, Miller Spring, is part of the Leland Harris Spring
Complex, but outflows of the two sites are not always connected.
(2) Gandy Salt Marsh: C.L., L.C., and E.L. Hubbs first collected
least chub at this site in 1942 (Sigler and Miller 1963, p. 82). Gandy
Salt Marsh is south of the Millard/Juab County line and the Leland
Harris Spring Complex and consists of private Utah School and
Institutional Trust Lands Administration (SITLA) and BLM lands.
Measuring approximately 6.4 kilometers (km) (4 miles (mi)) long (north
and south) and 3.2 km (2 mi) wide (east and west), the complex consists
of approximately 52 small springheads or ponds that drain into a large
playa wetland on approximately 1,295 hectares (ha) (3,200 acres (ac))
(BLM 1992, p. 11). Least chub is the dominant fish species at the Gandy
Salt Marsh site and comprises a wild self-sustaining population (Hines
et al. 2008, p. 40). However, the number of occupied sites within the
marsh has decreased about 50 percent since 1994 (Wilson 2006, p. 8;
Hines et al. 2008, p. 41).
(3) Bishop Springs Complex: Least chub were documented at this site
in 1942 (Hickman 1989, p. 18). The complex is now the largest occupied
least chub site in Snake Valley. Located south and very near Gandy Salt
Marsh, the site has large springs containing least chub, including
Central Spring and Twin Springs (Hines et al. 2008, p. 38). The least
chub population in Bishop Springs has remained stable and has
demonstrated successful reproduction and recruitment (Hines et al.
2008, p. 38). The manmade Foote Reservoir does not contain least chub
but contributes water to the playa marshlands that provide seasonal
least chub foraging, reproduction, and nursery-type habitat (Crawford
1979, pp. 62-65).
(4) Mills Valley: UDWR biologists discovered least chub at multiple
locations at this site in 1998 (Hines et al. 2008, p. 44). Mills Valley
is in the Sevier River drainage in southeast Juab County (Hines et al.
2008, p. 17). It consists of a wetland with numerous springheads
throughout the 200-ha (495-ac) complex. The least chub were present
during sampling from 2001 through 2006 (Hines et al. 2008, p. 44).
(5) Clear Lake: In 2003, UDWR biologists found least chub at the
Clear Lake Wildlife Management Area (WMA) in Millard County (Hines et
al. 2008, p. 45). This reserve consists of a shallow reservoir and
diked ponds fed by springs from adjacent Spring Lake. The site is
managed by UDWR for waterfowl habitat (Hines et al. 2008, p. 45).
Information about this least chub population is limited because of its
recent discovery; however, successful recruitment is occurring (Hines
et al. 2008, p. 45).
(6) Mona Springs: The UDWR biologists discovered this least chub
site in northeast Juab County in 1995 (Mock and Miller 2003, p. 3).
Mona Springs has provided habitat for a genetically distinct, naturally
occurring population of least chub. However, the Mona Springs site is
no longer suitable for least chub because of the presence of nonnative
fish; only four least chub were collected here in 2008 surveys (LCCT
2008a, p. 3). Because of the lack of population viability at this site,
we consider the least chub population at Mona Springs functionally
extirpated.
Translocations
In an attempt to create refuge (an artificial place of protection
for a species) populations and reestablish wild populations, 19
introductions of least chub to new locations rangewide were attempted
by UDWR between 1979 and 2008 (see table 3). Of these, two sites are
currently stable and secure (one has persisted for 3 years and another
for 1 year), seven introductions failed, and three are not secure. The
long-term success of seven of the transplants is currently unknown,
because they were initiated in 2008 and monitoring information is
limited. A description of each of the translocation efforts follows.
Table 3.--Least chub translocations attempted from 1979 to 2008.
Status categories:
Stable = viable self-sustaining population
Unstable = a limited number of least chub present but
population is not self-sustaining
Extirpated = least chub no longer present at location
Secure = no immediate threats present
Not secure = immediate threat(s) present
Unknown = no established sampling history
------------------------------------------------------------------------
Site Year Status
------------------------------------------------------------------------
Lakepoint Pond 1979 Extirpated
=================================
Harley Sanders Pond 1986 Extirpated
=================================
Red Butte Gardens 1987 Extirpated
=================================
Walter Springs 1995 Extirpated
=================================
Deadman Springs 1996 Extirpated
=================================
Antelope Island 2000 Extirpated
=================================
Lucin Pond 1989 Unstable - Not
secure
=================================
Garden Creek Pond 2004 Stable - Not
secure
=================================
Atherly Reservoir 2006 Unstable - Not
secure
=================================
Ibis/Pintail Ponds 2007 Extirpated
=================================
Red Knolls Pond 2005 Stable -
Secure
=================================
Willow Pond 2007 Stable -
Secure
=================================
Seven northern Utah sites 2008 Unknown
------------------------------------------------------------------------
(1) Lakepoint Pond, Tooele County: In 1979, 200 least chub from the
Leland Harris Spring Complex were released into Lakepoint Pond located
approximately 32 km (20 mi) southwest of Salt Lake City, 1.6 km (1 mi)
from the shore of the Great Salt Lake. This site was eliminated by
floods in 1983 and 1984 (Hickman 1989, p. 4).
(2) Harley Sanders Pond, Box Elder County: In 1986, UDWR released
least chub into Harley Sanders Pond and spring. No least chub were
found during sampling in 1988 (Hickman 1989, p. 4).
(3) Red Butte Gardens, Salt Lake County: In 1987, least chub were
introduced into the stream and pond at the Utah State Arboretum (Red
Butte
[[Page 35402]]
Gardens) near Fort Douglas in Salt Lake City (Hickman 1989, p. 5).
Attempts to relocate least chub in 1988 were unsuccessful (Hickman
1989, p. 5), so we consider it extirpated and unsuccessful.
(4, 5) Walter/Deadman Springs, Tooele County: Least chub were
introduced in 1995 and 1996 to these springs; however, they have been
replaced by western mosquitofish (Gambusia affinis) (Wilson and Whiting
2002, p. 4; Wilson and Mills 2004, pp. 4-5). Therefore, we consider
these sites to be extirpated and unsuccessful.
(6) Antelope Island, Davis County: In December 2000, UDWR
introduced least chub to a human-made spring-fed pond on Antelope
Island. Mosquitofish have replaced least chub at this site (Thompson
2005, pp. 5-6). Therefore, we consider this site to be extirpated and
unsuccessful.
(7) Lucin Pond, Box Elder County: In 1989, 42 least chub were
transplanted into this site. Lucin Pond is a human-made pond built in
the early 1900s. This least chub population is currently considered
unstable and not secure because mosquitofish are present and the water
supply to the pond is unreliable (Thompson 2005, pp. 1-4; Hines et al.
2008, pp. 47-49).
(8) Garden Creek Pond, Davis County: In 2004, 947 least chub were
introduced to this pond on Antelope Island in the Great Salt Lake. It
is a 0.04 ha (0.1 ac) pond that was dredged by the Utah Department of
Parks and Recreation and is fed by a perennial stream (stream with
continuous flow throughout the year). The site was considered a genetic
refuge for the functionally extirpated Mona Springs population.
Reproduction and recruitment have been occurring; however, the site is
threatened by a loss of habitat due to siltation (Thompson 2005, pp. 6-
7; Hines et al. 2008, p. 46; Thompson 2008, p. 3; LCCT 2008a, pp. 3-4).
(9) Atherly Reservoir, Tooele County: This site is on Faust Creek
in Rush Valley, and is part of the 283-ha (700-ac) James Walter
Fitzgerald WMA. Approximately 13,000 least chub from the Mills Valley
population were introduced in 2006 (Hines et al. 2008, p. 50). The UDWR
monitoring in 2008 detected only eight least chub (LCCT 2008a, p. 3).
Therefore, we do not consider this introduction to be successful at
this time.
(10) Ibis/Pintail Ponds, Tooele County: In 2007, least chub from
Leland Harris Spring Complex were introduced into Ibis and Pintail
Ponds on the Fish Springs National Wildlife Refuge (Hines et al. 2008,
p. 50). This introduction was unsuccessful, and the site currently does
not contain a least chub population. The UDWR is planning to release
least chub again in the future after mosquitofish control issues are
addressed (LCCT 2008a, p. 3).
(11) Red Knolls Pond, Box Elder County: In 2005, 250 least chub
from Bishop Springs were introduced to Red Knolls Pond (Hines et al.
2008, p. 50), located in the western portion of Box Elder County on BLM
land. Successful recruitment was observed in 2005, 2006, and 2007,
indicating that reproduction has been occurring (Hines et al. 2008, p.
50; Thompson 2008, p. 4). This site is currently secure and represents
a genetic refuge for the Bishop Springs Complex population.
(12) Willow Pond, Box Elder County: On August 22, 2007, 340 least
chub from the Clear Lake population were released into this habitat
(Hines et al. 2008, p. 50), located in the northwest portion of Box
Elder County. In 2008, least chub were present and recruitment to the
population was apparent (LCCT 2008a, p. 4). This site is currently
secure and represents a genetic refuge for the Clear Lake population.
(13) The UDWR introduced least chub into seven additional sites in
Cache and Box Elder Counties in 2008 (LCCT 2008a, p. 4). This effort
was conducted to establish new refuge populations by stocking State-
hatchery-produced least chub into suitable habitat. Success of these
introductions cannot be determined for several years; however, the
probability of success for some of these introductions may be low
because of the possibility of winter kill and the presence of nonnative
species.
In summary, we believe that translocated least chub populations can
contribute to the long-term conservation of the species by providing a
refuge (e.g., hatcheries or other managed systems) for the preservation
of a population's genetic diversity. In addition, translocation to a
refugium (a native habitat that has escaped ecological changes
occurring elsewhere and so provides a suitable habitat for a species)
contributes to long-term conservation of least chub by providing
conditions necessary to maintain a viable self-sustaining population.
However, to date, translocated least chub populations have had
relatively poor success because of problems with competing nonnative
fishes, inadequate water supply, or for unknown reasons (i.e., least
chub were stocked into a particular habitat but could not be relocated
during subsequent monitoring). While two populations have indications
of successful recruitment and are secure from immediate threats, it is
too early to determine whether these populations will contribute to the
long-term conservation of least chub. Monitoring of translocated
populations will be essential to address the uncertainty that exists
about the success of these actions. Due to the uncertainty of the long-
term status of translocated least chub populations, they are not
considered further in this review.
Hatchery Broodstock
The Wahweap Warmwater Fish Hatchery in Big Water, Utah, and the
Fisheries Experiment Station in Logan, Utah, each manage least chub
broodstock that were sourced from Mills Valley and Mona Springs (Hines
et al. 2008, p. 27). These hatcheries help preserve the genetic
diversity of source populations of least chub and provide stock for
introduction and reintroduction efforts.
Summary of Information Pertaining to the Five Factors
Section 4 of the Act (16 U.S.C. 1533), and implementing regulations
(50 CFR 424), set forth procedures for adding species to the Federal
Lists of Endangered and Threatened Wildlife and Plants. Under section
4(a)(1) of the Act, a species may be determined to be endangered or
threatened based on any of the following five factors: (A) The present
or threatened destruction, modification, or curtailment of its habitat
or range; (B) overutilization for commercial, recreational, scientific,
or educational purposes; (C) disease or predation; (D) the inadequacy
of existing regulatory mechanisms; or (E) other natural or manmade
factors affecting its continued existence. In making this finding,
information pertaining to the least chub in relation to the five
factors provided in section 4(a)(1) of the Act is discussed below.
Factor A. The Present or Threatened Destruction, Modification, or
Curtailment of the Species' Habitat or Range.
The following potential threats that may affect the habitat or
range of least chub are discussed in this section, including: (1)
Livestock grazing; (2) oil and gas leasing and exploration; (3) mining;
(4) urban and suburban development; (5) water withdrawal and diversion;
and (6) drought.
(1) Livestock Grazing
Grazing animals can impact aquatic habitats in multiple ways.
Livestock seek springs for food and water, both of which are limited in
desert habitats; therefore, they spend a disproportionate amount of
time in these areas (Stevens
[[Page 35403]]
and Meretsky 2008, p. 29). As they spend time at springs, livestock eat
and trample plants, compact local soils, and collapse banks of springs
(Stevens and Meretsky 2008, p. 29). Input of organic wastes increases
nutrient concentrations, and some nutrients (i.e., nitrogen compounds)
can become toxic to fish (Taylor et al. 1989, in Stevens and Meretsky
2008, p. 29). Domestic animals can also be trapped in soft spring
deposits, die and decompose, and pollute the water. All of these
effects can result in the loss or decline of native aquatic fauna
(Stevens and Meretsky 2008, pp. 29-30).
As explained below, historic livestock grazing impacted four of the
five remaining wild least chub sites, and current livestock grazing
practices continue to impact these sites. The UDWR monitors these sites
and is working on minimizing or removing livestock grazing threats
(Hines et al. 2008, pp. 22-23). Livestock grazing impacts occur at
Mills Valley (Wilson and Whiting 2002, pp. 2-3; Bailey 2006, p. 30;
Hines et al. 2008, p. 43), Gandy Salt Marsh (Hines et al. 2008, p. 39;
LCCT 2008b, p. 2), Miller Spring/Leland Harris Spring Complex (Bailey
2006, p. 11; Hines et al. 2008, pp. 41-42), and Bishop Springs/Foote
Reservoir/Twin Springs (Wheeler and Fridell 2005, p. 5). The Clear Lake
site is protected from livestock grazing because it is a WMA managed by
the State of Utah (Hines et al. 2008, p. 45).
Fencing at Gandy Salt Marsh and Miller Spring/Leland Harris Spring
Complex excludes cattle from springhead areas (Hines et al. 2008, pp.
39, 41, 43), but livestock damage still occurs at these sites during
periods of unmanaged overgrazing or when fences are not maintained
(Hines et al. 2008, p. 39; LCCT 2008b, p. 2). For example, in July
2008, livestock damage was reported to be extensive and fencing trapped
cattle inside the northern area of Gandy Salt Marsh (LCCT 2008b, p. 2).
Impacts from livestock grazing include bank erosion and
sedimentation to springheads (LCCT 2008b, p. 5). Miller Spring (at the
Leland Harris Spring Complex) was unsuitable for least chub due to
sedimentation and trampling associated with livestock use, poor water
quality, and the presence of rainbow trout (Hogrefe 2001, p. 7).
Extensive efforts by UDWR in 1999 and 2000 to restore and fence the
spring and remove nonnatives significantly improved the habitat
(Hogrefe 2001, pp. 7, 20); however, the response of least chub to
improvements at Miller Spring has not been determined. Most of the
other 12 to 15 springs in the Leland Harris Spring Complex have some
ungulate damage and bank disturbance (Hines et al. 2008, p. 42). A
rotational grazing plan has been developed with the landowner and UDWR
on 75 ha (188 ac) of the Leland Harris site to improve habitat
conditions, but damage to springs and riparian vegetation continues to
impact least chub habitat (Hines et al. 2008, p. 42).
Twin Springs, at the Bishop Spring complex, is partially protected
from livestock by fences, but the larger spring complex, Twin Springs
South, is not protected from grazing or wild horse watering access.
Twin Springs South has severely impacted banks resulting in shallower
water, increased surface area, and sedimentation of spring heads
(Wheeler et al. 2004, p. 5). On the State-owned WMA portion of the
Mills Valley site, grazing is allowed in return for access across
private land. The private portion of Mills Valley is overgrazed and
damage to water body banks and riparian vegetation has been reported as
moderate to severe (UDWR 2006, pp. 27-28). The BLM has built fencing
around two Gandy Salt Marsh springheads, Pilot Springs and Red Knolls
Pond, to protect least chub transplant locations (Hines et al. 2008, p.
24).
In summary, our analysis indicates that, although efforts to
control and minimize damage have been implemented and are ongoing,
livestock grazing impacts some habitat at most wild least chub sites.
Grazing damage is not always severe where it occurs, and livestock are
effectively excluded from portions of occupied habitat. However,
extensive livestock grazing-related damage has occurred in the last
couple of years in some instances, and livestock grazing on private
lands where least chub occur is still partially unregulated. Therefore,
we conclude that current levels of livestock grazing are likely to
significantly threaten least chub populations at Leland Harris Spring
Complex, Gandy Salt Marsh, Bishop Springs Complex, and Mills Valley,
now and in the foreseeable future.
(2) Oil and Gas Leasing and Exploration
Oil and gas leasing and exploration can have direct and indirect
impacts on springs, marshes, and riparian habitats. Vehicles, including
drilling rigs and recording trucks, can crush vegetation, compact
soils, and introduce exotic plant species (BLM 2008, pp. 4-9 to 4-20).
Roads and well pads can affect local drainages and surface hydrology,
and increase erosion and sedimentation (Matherne 2006, p. 35).
Accidental spills (Etkin 2009, pp. 36-42, 56) can result in the release
of hydrocarbon products into ground and surface waters (Stalfort 1998,
section 1). Accumulations of contaminants in floodplains can result in
lethal or sublethal impacts to endemic sensitive aquatic species
(Stalfort 1998, section 4; Fleeger et al. 2003, p. 207).
All of the naturally occurring, extant least chub populations occur
within the Fillmore BLM area. The majority of BLM land in the Fillmore
Field Office is open to oil and gas leasing (BLM 2009a, p. 11). Oil and
gas leases have been sold within the watershed areas of most of the
naturally occurring least chub populations, but the closest active well
to a least chub population is currently 9.7 km (6 mi) away (Megown
2009a, entire). The Gandy Salt Marsh population area is closed to
leasing by BLM in accordance with the Fillmore Resource Management Plan
(RMP) because of the occurrence of least chub habitat. This RMP will be
updated in approximately 10 to 15 years. Any change to the management
direction would be reviewed at this time and subject to public comment
(BLM 2009a, p. 54). Seismic surveys were conducted on parcels adjacent
to the Mills Valley population, and BLM anticipates that a Notice of
Staking or Application for Permit to Drill may be filed by the lessee
in 2010 (Mansfield 2009, p. 1).
Based on past drilling history, the BLM's Fillmore Field Office
determined that recoverable oil and gas is likely to be of low
availability within the range of the least chub. They further estimated
that exploratory wells will be drilled at the rate of about one well
every year for the foreseeable future (BLM 2009a, p. 52). Leases near
least chub habitat will not be offered for sale until the Fillmore BLM
RMP is revised; the RMP revision is not yet scheduled (Naeve 2009a-c,
entire).
Oil and gas leases in the BLM Fillmore Field Office will include
lease notices with information on sensitive species and conservation
agreement species where appropriate (BLM 2009a, pp. 14, 98-99). These
lease notices include measures to coordinate with UDWR to minimize the
risk of spreading aquatic exotic species; avoid surface pumping for
water; avoid surface disturbances within 100-year floodplains; avoid
changes to ground and surface hydrology; and avoid direct disturbances
to special status species (BLM 2009a, pp. 98-99). The extent of
implementation of each lease notice, and the success of the lease
notices, will not be known until development occurs. However, the lease
notices in combination with the low energy development potential should
ensure that oil and gas development is not a significant threat to the
species in the
[[Page 35404]]
foreseeable future. Recoverable oil and gas across the entire Fillmore
Field Office area is expected to be low, with a rate of one exploratory
well drilled annually, and the nearest active well is 9.7 km (6 mi)
from an extant least chub population. We conclude that oil and gas
development are not anticipated to occur at a level that will threaten
least chub.
(3) Mining
Mills Valley contains a bog area with a peat and humus resource
(Olsen 2004, p. 6). Peat mining has the potential to alter the
hydrology and habitat complexity of Mills Valley, making it unsuitable
for least chub (Bailey et al. 2005, p. 31). An illegal peat removal
activity occurred on private lands in the Mills Valley wetlands in 2003
(Wilson 2009a, pers. comm.). The illegal activity was less than 0.2 ha
(0.5 ac) in size, and impacts to associated wetlands were restored
(Wilson 2009a, pers. comm.). In 2003, a Mills Valley landowner received
a permit from the Utah Division of Oil, Gas, and Mining to conduct peat
mining on their private land. Although one test hole was dug, no
further peat mining occurred in this location. This peat mining permit
is now inactive and noncompliant with State regulations requiring
payment of mining and bond fees (Wilson 2009a, pers. comm.). Past peat
mining activities have been unsuccessful in Mills Valley, and we are
unaware of any future private or commercial peat mining proposals.
In summary, our analysis found one illegal peat removal activity
and one abandoned attempt at legal peat removal in the Mills Valley
least chub population area. We are unaware of any additional private or
commercial peat operation proposals in Mills Valley. We conclude that
peat mining is not anticipated to occur at a level that will threaten
least chub.
(4) Urban and Suburban Development
Urban and suburban development affect least chub habitats through:
(1) Changes to hydrology and sediment regimes; (2) inputs of pollution
from human activities (contaminants, fertilizers, and pesticides); (3)
introductions of nonnative plants and animals; and (4) alterations of
springheads, stream banks, floodplains, and wetland habitats by
increased diversions of surface flows and connected groundwater (Dunne
and Leopold 1978, pp. 693-702).
The least chub was originally common throughout the Bonneville
Basin in a variety of habitat types (Sigler and Miller 1963, p. 82). In
many urbanized and agricultural areas, residential development and
water development projects have effectively eliminated historical
habitats and potential reintroduction sites for least chub (Keleher and
Barker 2004, p. 4; Thompson 2005, p. 9). Development and urban
encroachment have either functionally or completely eliminated most
springs, streams, and wetlands along the Wasatch Front (Keleher and
Barker 2004, p. 2).
The Mona Springs site, as well as potential reintroduction sites
(Keleher and Barker 2004, p. 4; Thompson 2005, p. 9) on the Wasatch
Front, are vulnerable to rapid population growth. The human population
in the Mona Springs area has increased 64.9 percent from 2000 to mid
2008 (City-Data 2009, p. 1) and a housing development has expanded to
within 1 km (0.6 mi) of the Mona Springs least chub site (Megown 2009b,
entire). The URMCC, which is responsible for mitigating impacts caused
by Federal reclamation projects to fish, wildlife, and related
recreation resources in Utah, has purchased and protected much of the
Mona Springs habitat areas for conserving least chub and spotted frog
populations (see Factor D). However, indirect effects of urban
development such as pollution from urban stormwater runoff and changes
to hydrologic sediment regimes (e.g., sedimentation from adjacent
construction activities) could negatively impact the aquatic habitats
at Mona Springs. Even if mosquitofish and other predacious nonnative
fish (the primary threat at this site) can be controlled in the future,
we believe urban-development-related effects could rise to a level that
may preclude reestablishment of a viable least chub population at Mona
Springs.
Despite the effects of urban and suburban development on historic
populations of least chub, we have no information indicating this is a
threat to the five remaining extant least chub populations. These least
chub populations occur in relatively remote portions of Utah with
minimal human populations. No information is available indicating the
level of human occupation near these sites. However, the population
centers nearest to extant least chub populations are more than 16 km
(10 mi) away and have populations of less than 3,000 persons (Utah
Governor's Office of Planning and Budget 2009, entire).
To summarize, development along the eastern portion of the least
chub historic range has contributed to the elimination of most of the
historic populations of least chub. The Mona Springs site is currently
the only site in this geographic area that still contains least chub,
but the population is functionally extirpated. We have no information
suggesting that future urban or suburban development will occur at a
level that will threaten least chub.
(5) Water Withdrawal and Diversion
Hydrologic alterations, including water withdrawal and diversion,
affect a variety of abiotic and biotic factors that regulate least chub
population size and persistence. Abiotic factors include physical and
chemical characteristics of the environment, such as water levels and
temperature, while biotic factors include interactions with other
individuals or other species (Deacon 2007, pp. 1-2). Water withdrawal
directly reduces available habitat, impacting water depth, water
surface area, and flows from springheads (Alley et al. 1999, p. 43). As
available habitat decreases, the characteristics and value of the
remaining habitat changes. Reductions in water availability to least
chub habitat reduce the quantity and quality of the remaining habitat
(Deacon 2007, p. 1).
Water withdrawal and diversion reduces the size of ponds, springs,
and other water features that support least chub (Alley et al. 1999, p.
43). Assuming that the habitat remains at carrying capacity for the
species or, in other words, assuming all population processes (birth
rate, death rate, etc.) remain unchanged, smaller habitats support
fewer individuals by offering fewer resources for the population
(Deacon 2007, p. 1).
Because least chub live in patchily distributed desert aquatic
systems, reduction in habitat size also affects the quality of the
habitat. Reduced water depth may isolate areas that would be
hydrologically connected at higher water levels. Within least chub
habitat, springheads offer stable environmental conditions, such as
temperature and oxygen levels, for refugia and overwintering, but offer
little food or vegetation (Deacon 2007, p. 2). In contrast, marsh areas
offer vegetation for spawning and feeding, but exhibit wide
fluctuations in environmental conditions (Crawford 1979, p. 63; Crist
and Holden 1980, p. 804). Maintaining hydrologic connections between
springheads and marsh areas is important because least chub migrate
between these areas to access the full range of their ecological
requirements (Crawford 1979, p. 63; Crist and Holden 1980, p. 804;
Lamarra 1981, p. 10).
Although we have not directly observed the effects of flow
reductions on wild least chub populations, we believe that flow
reductions will reduce the hydrology that supports wetland
[[Page 35405]]
and wetland/upland transition zones which, in turn, provide vegetation
needed for the least chub reproductive cycle (Crawford 1979, p. 38;
Lamarra 1981, p. 10). Alterations of natural flow processes also could
alter sediment transport processes that prevent vegetation encroachment
into sensitive spring areas (60 FR 50520).
Reductions in water may alter chemical and physical properties of
aquatic habitats. As water quantity decreases, temperatures may rise
(especially in desert ecosystems with little shade cover), dissolved
oxygen may decrease, and the concentration of pollutants may increase
(Alley et al. 1999, p. 41; Deacon 2007, p. 1). These modified habitat
conditions are likely to significantly impact least chub life history
processes, possibly beyond the state at which the species can survive.
The maximum growth rate for least chub less than 1 year of age would
occur at 22.3 [deg]C (72.1 [deg]F). Temperatures above or below this
have the potential to negatively impact growth and affect survival
rates (Billman et al. 2006, p. 438).
Reduced habitat quality and quantity may cause niche overlaps with
other fish species, increasing hybrid introgression, interspecific
competition, and predation (Deacon 2007, p. 2) (see Factor C.
Predation; Factor E. Hybridization). Reduction in flow of springs
reduces opportunities for habitat niche partitioning; therefore, fewer
species are able to coexist. The effect is especially problematic with
respect to introduced species. Native species may be able to coexist
with introduced species in relatively large habitats (see Factor C.
Predation), but become increasingly vulnerable to extirpation as
habitat size diminishes (Deacon 2007, p. 2).
Habitat reduction may affect the species by altering individual
success. Fish and other aquatic species tend to adjust their maximum
size to the amount of habitat available, so reduced habitat may reduce
the growth capacity of least chub (Smith 1981, in Deacon 2007, p. 2).
Reproductive output decreases exponentially as fish size decreases
(Deacon 2007, p. 2). Therefore, reduction of habitat volume in isolated
desert springs and streams reduces reproductive output (Deacon 2007, p.
2). Longevity also may be reduced resulting in fewer reproductive
seasons (Deacon 2007, p. 2).
Current Groundwater Pumping
The Utah State Engineer (USE), through the Utah Division of Water
Rights (UDWRi), is responsible for the administration of water rights,
including the appropriation, distribution, and management of the
State's surface and groundwater. This office has broad discretionary
powers to implement the duties required by the office. The USE's Office
was created in 1897, and the State Engineer is the chief water rights
administrative officer. For groundwater management, Utah is divided
into groundwater areas, and policy is determined by area (BLM 2009b,
entire).
A joint report by the U.S. Geological Survey (USGS) and several
State of Utah agencies provided a description of groundwater conditions
in the State of Utah for 2008 (Burden 2009, entire). Each of the
locations occupied by least chub had a corresponding summary by valley
or hydrographic area for: the number of wells constructed in 2008; the
total estimated groundwater withdrawn in the area for 2008; the total
estimated groundwater withdrawn for each year for the previous 10
years; and groundwater level monitoring results from several monitoring
wells for varying periods of record (~20 to 75 years). For all valleys
and hydrographic areas, the predominant (greater than 79 percent) use
of withdrawn groundwater was for irrigation with remaining uses
including industrial, public supply, domestic, and stock (Burden 2009,
pp. 5, 89).
The Juab Valley, where the Mona Springs least chub site is located,
had a total of two new wells, and 26,000 acre-feet per year (afy)
withdrawn for 2008 (Burden 2009, pp. 3-5). This is more than double the
amount withdrawn in 1998 (12,000 afy) and is an overall increase from
the 1998-2007 average (22,000 afy) (Burden 2009, p. 6). All supplies of
surface and groundwater are fully appropriated; however, new wells
could be developed with existing groundwater rights (UDWRi 2009d, pp.
1-2).
Although the Mills Valley population site did not have a
corresponding pumping area in the report, the Central Sevier Valley
summary represents pumping activity in the river valley upstream of
this population and may be indicative of the potential for groundwater
withdrawal effects. The Central Sevier Valley had a total of 13 new
wells, and 24,000 afy withdrawn in 2008 (Burden 2009, pp. 3-5). This is
4,000 afy more than the amount withdrawn in 1998 (20,000 afy) and is an
8,000-afy increase from the 1998-2007 average (16,000 afy) (Burden
2009, p. 6). Since 1997, the corresponding part of the Sevier River
Basin was closed to all new appropriations of groundwater. However, new
groundwater development can occur under existing groundwater rights
(UDWRi 2009d, pp. 3-4).
The Clear Lake least chub site is located within the Sevier Desert
groundwater pumping basin, which had 11 new wells with 44,000 afy
withdrawn in 2008 (Burden 2009, pp. 3-5). This is 32,000 afy more than
the amount of water withdrawn in 1998 (12,000 afy) and is a 20,000-afy
increase from the 1998-2007 average (24,000 afy) (Burden 2009, p. 6).
Since 1997, this part of the Sevier River Basin was closed to all new
appropriations of groundwater except for domestic filings not exceeding
1.0 acre-foot and for filings reviewed on an individual basis in
limited areas of the basin (UDWRi 2009d, pp. 5-6).
The Snake Valley summary, which corresponds to the pumping activity
in the vicinity of Leland Harris Spring Complex, Gandy Salt Marsh, and
Bishop Spring Complex did not report the number of new wells, but did
specify 19,800 and 20,200 afy withdrawn for 2007 and 2008,
respectively, in Utah (Burden 2009, p. 89). Additional information on
groundwater pumping over the last decade was not provided. State of
Nevada Division of Water Resources reported that 11,000 afy of
groundwater was pumped from the Nevada portion of Snake Valley in 2009
(NDWR 2009, entire). Groundwater is currently open to appropriation in
Snake Valley in Utah (UDWRi 2009d, pp. 7-9) and Nevada (NDWR 2009,
entire).
The previously discussed increases in groundwater pumping have
occurred at the same time that a declining trend in groundwater level
was observed at wells monitored in or very near basins with least chub
populations (Burden 2009, pp. 41-57, 89, 96). Groundwater monitoring
shows that water levels generally rose in the early to mid 1980s,
likely as a result of greater-than-average precipitation. However,
groundwater levels generally declined from the mid-to-late 1980s to the
present. Although drought conditions were present in the eastern Great
Basin (areas with extant least chub populations) during this time (See
Factor A. Drought), localized annual precipitation levels were either
average to slightly above average (Mona Springs and Mills Valley least
chub sites) or were generally increasing, if below average (Clear Lake
and Snake Valley least chub sites), during this same timeframe (Burden
2009, pp. 41-57, 89, 96).
For the four basins discussed above, a more specific analysis of
groundwater level fluctuations over the last decade (1998-2009)
provides some indication of the scope of change. Groundwater
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levels from six monitoring wells in Juab Valley (where the Mona Springs
least chub site is located) declined an average of 6.1 meters (m) (20
feet (ft)) with declines ranging from 0.6 to 10.1 m (2 to 33 ft)
(Burden 2009, pp. 41-45). As stated above, groundwater monitoring in
Central Sevier Valley basin represents pumping activity and groundwater
levels in the river valley upstream of the Mills Valley least chub
population and may be indicative of the potential for groundwater
withdrawal effects. Groundwater levels in 10 monitoring wells in this
area declined an average of 0.9 m (3 ft) with declines ranging from 0
to 1.5 m (0 to 5 ft). Data from 15 monitoring wells in the Sevier
Desert groundwater pumping basin (where the Clear Lake least chub site
is located) indicated that groundwater levels declined an average of
2.4 m (8 ft) with declines ranging from 0.3 to 5.5 m (1 to 18 ft), and
groundwater monitoring levels in the Snake Valley (in the vicinity of
Leland Harris Spring Complex, Gandy Salt Marsh, and Bishop Spring
Complex) declined 1.2 m (4 ft) with declines ranging from 0.3 to 3 m (1
to 10 ft) (Burden 2009, pp. 46-52, 89-96).
We have limited information linking groundwater pumping to
decreases in flow at sites where least chub previously existed.
Agricultural pumping, combined with drought, has affected several
springs in Snake Valley. These include Knoll Spring near the town of
Eskdale and springs on private properties in the town of Callao (Sabey
2008, p. 2). These sites were all historically documented locations of
least chub that no longer harbor the species (Hickman 1989, pp. 16-17;
Garland 2007, pers. comm.).
Pumping for agricultural purposes, combined with the effects of
drought, has impacted flow in a number of springs in Snake Valley.
Although no least chub historically occurred at Needle Point Spring,
the BLM has detailed monitoring information linking nearby groundwater
pumping and its effect on the spring's flow. In 2001, the water level
at Needle Point Spring in Southern Snake Valley dropped to levels not
seen in 40 years (Summers 2008, pp. 1-2). This spring has a long
history of existence, identified as early as 1939 by the Civilian
Conservation Corps, when springflow was measured at 6 gallons per
minute (Summers 2008, p. 1). For the past several decades, the spring
was developed and used for watering livestock and wild horses (Summers
2008, p. 1). The 2001 decline in groundwater level at Needle Point
Spring was likely the result of, and coincides with, increased
irrigation in Hamlin Valley approximately 3.2 km (2 mi) west, and not a
result of the lowered precipitation (Summers 2008, p. 3).
Although the causal effect of groundwater pumping is unknown in the
following observations, UDWR has documented decreases in habitat at two
least chub sites. They recently reported decreases in least chub
habitat from springs drying and decreasing in size at the Clear Lake
least chub site (LCCT 2008b, p. 2). The UDWR found that annual drying
of some ponds with least chub is becoming a consistent trend resulting
in declining habitat quality, and is therefore