Endangered and Threatened Wildlife and Plants; Determination for the Gunnison Sage-grouse as a Threatened or Endangered Species, 59804-59863 [2010-23430]
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Information Relay Service (FIRS) at
800–877–8339.
SUPPLEMENTARY INFORMATION:
DEPARTMENT OF THE INTERIOR
Fish and Wildlife Service
50 CFR Part 17
[DOCKET NO. FWS-R6-ES-2009-0080]
MO 92210-0-0008
Endangered and Threatened Wildlife
and Plants; Determination for the
Gunnison Sage-grouse as a
Threatened or Endangered Species
Fish and Wildlife Service,
Interior.
ACTION: Notice of the results of a status
review.
AGENCY:
We, the U.S. Fish and
Wildlife Service (Service), announce our
12–month finding on whether to list the
Gunnison sage-grouse (Centrocercus
minimus) as threatened or endangered
under the Endangered Species Act of
1973, as amended (Act). After reviewing
the best available scientific and
commercial information, we find that
the species is warranted for listing.
Currently, however, listing the
Gunnison sage-grouse is precluded by
higher priority actions to amend the
Lists of Endangered and Threatened
Wildlife and Plants. Upon publication
of this 12-month finding, we will add
the Gunnison sage-grouse to our
candidate species list. We will develop
a proposed rule to list this species as
our priorities allow. We will make any
determination on critical habitat during
development of the proposed listing
rule.
SUMMARY:
The determination announced in
this document was made on September
28, 2010.
ADDRESSES: This finding is available on
the Internet at https://
www.regulations.gov at Docket Number
FWS-R6-ES-2009-0080. 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, Western Colorado
Ecological Services Field Office, U.S.
Fish and Wildlife Service, 764 Horizon
Drive, Building B, Grand Junction,
Colorado 81506-3946. Please submit any
new information, materials, comments,
or questions concerning this finding to
the above address.
FOR FURTHER INFORMATION CONTACT:
Allan Pfister, Western Colorado
Supervisor (see ADDRESSES section); by
telephone at (970) 243-2778 ext. 29; or
by facsimile at (970) 245-6933. If you
use a telecommunications device for the
deaf (TDD), please call the Federal
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Background
Section 4(b)(3)(A) 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
that listing a species may be warranted,
we make a finding within 12 months of
the date of receipt of the petition. In this
finding, we determine whether 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
On January 18, 2000, we designated
the Gunnison sage-grouse as a candidate
species under the Act, with a listing
priority number of 5. However,
Candidate Notices of Review (CNOR)
are only published annually; therefore,
the Federal Register notice regarding
this decision was not published until
December 28, 2000 (65 FR 82310).
Candidate species are plants and
animals for which the Service has
sufficient information on their
biological status and threats to propose
them as endangered or threatened under
the Act, but for which the development
of a proposed listing regulation is
precluded by other higher priority
listing activities. A listing priority of 5
is assigned to species with high
magnitude threats that are nonimminent.
On January 26, 2000, American Lands
Alliance, Biodiversity Legal Foundation,
and others petitioned the Service to list
the Gunnison sage-grouse (Webb 2000,
pp. 94-95). In 2003, the U.S. District
Court ruled that the species was
designated as a candidate by the Service
prior to receipt of the petition, and that
the determination that a species should
be on the candidate list is equivalent to
a 12-month finding (American Lands
Alliance v. Gale A. Norton, C.A. No. 00-
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2339, D. D.C.). Therefore, we did not
need to respond to the petition.
In the 2003 CNOR, we elevated the
listing priority number for Gunnison
sage-grouse from 5 to 2 (69 FR 24876;
May 4, 2004), as the imminence of the
threats had increased. In the subsequent
CNOR (70 FR 24870; May 11, 2005), we
maintained the listing priority number
for Gunnison sage-grouse as a 2. A
listing priority number of 2 is assigned
to species with high magnitude threats
that are imminent.
Plaintiffs amended their complaint in
May 2004, to allege that the Service’s
warranted but precluded finding and
decision not to emergency list the
Gunnison sage-grouse were in violation
of the Act. The parties filed a stipulated
settlement agreement with the court on
November 14, 2005, which included a
provision that the Service would make
a proposed listing determination by
March 31, 2006. On March 28, 2006, the
plaintiffs agreed to a one-week
extension (April 7, 2006) for this
determination.
In April 2005, the Colorado Division
of Wildlife (CDOW) applied to the
Service for an Enhancement of Survival
Permit for the Gunnison sage-grouse
pursuant to section 10(a)(1)(A) of the
Act. The permit application included a
proposed Candidate Conservation
Agreement with Assurances (CCAA)
between CDOW and the Service. The
standard that a CCAA must meet is that
the ‘‘benefits of the conservation
measures implemented under a CCAA,
when combined with those benefits that
would be achieved if it is assumed that
conservation measures were also to be
implemented on other necessary
properties, would preclude or remove
any need to list the species.’’ The CCAA,
the permit application, and the
Environmental Assessment were made
available for public comment on July 6,
2005 (70 FR 38977). The CCAA and
Environmental Assessment were
finalized in October 2006, and the
associated permit was issued on October
23, 2006. Landowners with eligible
property in southwestern Colorado who
wish to participate can voluntarily sign
up under the CCAA and associated
permit through a Certificate of Inclusion
by providing habitat protection or
enhancement measures on their lands. If
the Gunnison sage-grouse is listed under
the Act, the permit authorizes incidental
take of Gunnison sage-grouse due to
otherwise lawful activities in
accordance with the terms of the CCAA
(e.g., crop cultivation, crop harvesting,
livestock grazing, farm equipment
operation, commercial/residential
development, etc.), as long as the
participating landowner is performing
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activities identified in the Certificate of
Inclusion. Four Certificates of Inclusion
have been issued by the CDOW and
Service to private landowners to date.
On April 11, 2006, the Service
determined that listing the Gunnison
sage-grouse as a threatened or
endangered species was not warranted
and published the final listing
determination in the Federal Register
on April 18, 2006 (71 FR 19954).
Consequently, we removed Gunnison
sage-grouse from the candidate species
list at the time of the final listing
determination. On November 14, 2006,
Plaintiffs (the County of San Miguel,
Colorado; Center for Biological
Diversity; WildEarth Guardians; Public
Employees for Environmental
Responsibility; National Audubon
Society; The Larch Company; Center for
Native Ecosystems; Sinapu; Sagebrush
Sea Campaign; Black Canyon Audubon
Society; and Sheep Mountain Alliance)
filed a Complaint for Declaratory and
Injunctive relief, pursuant to the Act,
and on October 24, 2007, filed an
amended Complaint for Declaratory and
Injunctive relief, alleging that the 12–
month finding on the Gunnison sagegrouse violated the Act. On August 18,
2009, a stipulated settlement agreement
and Order was filed with the court, with
a June 30, 2010, date by which the
Service shall submit to the Federal
Register a 12–month finding, pursuant
to 16 U.S.C. § 1533(b)(3)(B), that listing
the Gunnison sage-grouse under the Act
is (a) warranted; (b) not warranted; or (c)
warranted but precluded by higher
priority listing actions. We published a
notice of intent to conduct a status
review of Gunnison sage-grouse on
November 23, 2009 (74 Fr 61100). The
Court approved an extension of the June
30, 2010, deadline for the 12–month
finding to September 15, 2010.
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Additional Special Status
Considerations
The Gunnison sage-grouse has an
International Union for Conservation of
Nature (IUCN) Red List Category of
‘‘endangered’’ (Birdlife International
2009). NatureServe currently ranks the
Gunnison sage-grouse as G1—Critically
Imperiled (Nature Serve 2010, entire).
The Gunnison sage-grouse is on the
National Audubon Society’s WatchList
2007 Red Category which is ‘‘for species
that are declining rapidly or have very
small populations or limited ranges, and
face major conservation threats.’’
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Biology and Ecology of Gunnison Sagegrouse
Gunnison Sage-grouse Species
Description
Sage-grouse are the largest grouse in
North America. Sage-grouse (both
greater and Gunnison) are most easily
identified by their large size, dark
brown color, distinctive black bellies,
long pointed tails, and association with
sagebrush habitats. They are dimorphic
in size, with females being smaller. Both
sexes have yellow-green eye combs,
which are less prominent in females.
Sage-grouse are known for their
elaborate mating ritual where males
congregate on strutting grounds called
leks and ‘‘dance’’ to attract a mate.
During the breeding season, males have
conspicuous filoplumes (specialized
erectile feathers on the neck), and
exhibit yellow-green apteria (fleshy bare
patches of skin) on their breasts
(Schroeder et al. 1999, p. 2, 18).
Gunnison sage-grouse are smaller in
size, have more white barring in their
tail feathers, and have more filoplumes
than greater sage-grouse.
Since Gunnison and greater sagegrouse were only recognized as separate
species in 2000, the vast majority of the
research relative to the biology and
management of the two species has been
conducted on greater sage-grouse.
Gunnison sage-grouse and greater sagegrouse have similar life histories and
habitat requirements (Young 1994, p.
44). In this finding, we use information
specific to the Gunnison sage-grouse
where available but still apply scientific
management principles found relevant
for greater sage-grouse to Gunnison
sage-grouse management needs and
strategies, a practice followed by the
wildlife agencies that have
responsibility for management of both
species and their habitat.
Taxonomy
Gunnison sage-grouse and greater
sage-grouse are members of the
Phasianidae family. For many years,
sage-grouse were considered a single
species. Gunnison sage-grouse
(Centrocercus minimus) were identified
as a distinct species based on
morphological (Hupp and Braun 1991,
pp. 257-259; Young et al. 2000, pp. 447448), genetic (Kahn et al. 1999, pp. 820821; Oyler-McCance et al. 1999, pp.
1460-1462), and behavioral (Barber
1991, pp. 6-9; Young 1994; Young et al.
2000, p. 449-451) differences and
geographical isolation (Young et al.
2000, pp. 447-451). Based on these
differences, the American
Ornithologist’s Union (2000, pp. 849850) accepted the Gunnison sage-grouse
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as a distinct species. The current ranges
of the two species do not overlap
(Schroeder et al. 2004, p. 369). Due to
the several lines of evidence separating
the two species cited above, we
determined that the best available
information indicates that the Gunnison
sage-grouse is a valid taxonomic species
and a listable entity under the Act.
Life History Characteristics
Gunnison and greater sage-grouse
depend on a variety of shrub-steppe
habitats throughout their life cycle and
are considered obligate users of several
species of sagebrush (Patterson 1952, p.
42; Braun et al. 1976, p. 168; Schroeder
et al. 1999, pp. 4-5; Connelly et al.
2000a, pp. 970-972; Connelly et al.
2004, p. 4-1, Miller et al. in press, p. 10).
Dietary requirements of the two species
are also similar, being composed of
nearly 100 percent sagebrush in the
winter, and forbs and insects as well as
sagebrush in the remainder of the year
(Wallestad et al. 1975, p. 21; Schroeder
et al. 1999, p. 5; Young et al. 2000, p.
452). Gunnison and greater sage-grouse
do not possess muscular gizzards and,
therefore, lack the ability to grind and
digest seeds (Leach and Hensley 1954,
p. 389).
In addition to serving as a primary
year-round food source, sagebrush also
provides cover for nests (Connelly et al.
2000a, pp. 970-971). Thus, sage-grouse
distribution is strongly correlated with
the distribution of sagebrush habitats
(Schroeder et al. 2004, p. 364). Connelly
et al. (2000a, p. 970-972) segregated
habitat requirements into four seasons:
(1) breeding (2) summer - late broodrearing (3) fall and (4) winter.
Depending on habitat availability and
proximity, some seasonal habitats may
be indistinguishable. The Gunnison
Sage-grouse Rangewide Steering
Committee (GSRSC) (2005, p. 27-31)
segregated habitat requirements into
three seasons: (1) breeding (2) summer–
late fall and (3) winter. For purposes of
this finding, the seasons referenced in
GSRSC (2005) are used because that
publication deals specifically with
Gunnison sage-grouse.
Sage-grouse exhibit strong site fidelity
(loyalty to a particular area) to seasonal
habitats, which includes breeding,
nesting, brood rearing, and wintering
areas, even when the area is no longer
of value (Connelly et al. 2004, p. 3-1).
Adult sage-grouse rarely switch among
these habitats once they have been
selected, limiting their adaptability to
changes. Sage-grouse distribution is
associated with sagebrush (Schroeder et
al. 2004 p. 364), although sagebrush is
more widely distributed than sagegrouse because sagebrush does not
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always provide suitable habitat due to
fragmentation and degradation
(Schroeder et al. 2004, pp. 369, 372).
Very little of the extant sagebrush in
North America is undisturbed, with up
to 50 to 60 percent having altered
understories (forb and grass vegetative
composition under the sagebrush) or
having been lost to direct conversion
(Knick et al. 2003, p. 612 and references
therein). Mapping altered and depleted
understories is challenging, particularly
in semi-arid regions, so maps depicting
only sagebrush as a dominant cover type
are deceptive in their reflection of
habitat quality and, therefore, use by
sage-grouse (Knick et al. 2003, p. 616
and references therein). As such,
variations in the quality of sagebrush
habitats for sage-grouse (from either
abiotic or anthropogenic events) are
better reflected by sage-grouse
distribution and densities, rather than
by broad geographic scale maps of the
distribution of sagebrush.
Sage-grouse exhibit a polygamous
mating system where a male mates with
several females. Males perform
courtship displays and defend their leks
(Patterson 1952, p. 83). Lek displaying
occurs from mid-March through late
May, depending on elevation (Rogers
1964, p. 21; Young et al. 2000, p. 448).
Numerous researchers have observed
that a relatively small number of
dominant males account for the majority
of copulations on each lek (Schroeder et
al. 1999, p. 8). However, an average of
45.9 percent (range 14.3 to 54.5 percent)
of genetically identified males in a
population fathered offspring in a given
year (Bush 2009, p. 106). This more
recent work suggests that males and
females likely engage in off-lek
copulations. Males do not incubate eggs
or assist in chick rearing.
Lek sites can be located on areas of
bare soil, wind-swept ridges, exposed
knolls, low sagebrush, meadows, and
other relatively open sites with good
visibility and low vegetation structure
(Connelly et al. 1981, pp. 153-154; Gates
1985, pp. 219-221; Klott and Lindzey
1989, pp. 276-277; Connelly et al. 2004,
pp. 3-7 and references therein). In
addition, leks are usually located on flat
to gently sloping areas of less than 15
percent grade (Patterson 1952, p. 83;
Giezentanner and Clark 1974, p. 218;
Wallestad 1975, p. 17; Autenrieth 1981,
p. 13). Leks are often surrounded by
denser shrub-steppe cover, which is
used for escape, and thermal and
feeding cover. Leks can be formed
opportunistically at any appropriate site
within or adjacent to nesting habitat
(Connelly et al. 2000a, p. 970). Lek
habitat availability is not considered to
be a limiting factor for sage-grouse
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(Schroeder 1997, p. 939). However,
adult male sage-grouse demonstrate
strong yearly fidelity to lek sites
(Patterson 1952, p. 91; Dalke 1963 et al.,
pp. 817-818), and some Gunnison sagegrouse leks have been used since the
1950s (Rogers 1964, pp. 35-40).
The pre-laying period is from lateMarch to April. Pre-laying habitats for
sage-grouse need to provide a diversity
of vegetation including forbs that are
rich in calcium, phosphorous, and
protein to meet the nutritional needs of
females during the egg development
period (Barnett and Crawford 1994, p.
117; Connelly et al. 2000a, p. 970).
During the pre-egg laying period, female
sage-grouse select forbs that generally
have higher amounts of calcium and
crude protein than sagebrush (Barnett
and Crawford 1994, p. 117).
Nesting occurs from mid-April to
June. Average earliest nest initiation
was April 30, and the average latest nest
initiation was May 19, in the western
portion of the Gunnison Basin (Childers
2009, p. 3). Radio-tracked Gunnison
sage-grouse nest an average of 4.3
kilometers (km ) (2.7 miles (mi)) from
the lek nearest to their capture site, with
almost half nesting within 3 km (2 mi)
of their capture site (Young 1994, p. 37).
Nest sites are selected independent of
lek locations, but the reverse is not true
(Bradbury et al. 1989, p. 22; Wakkinen
et al. 1992, p. 382). Thus, leks are
indicative of nesting habitat. Eightyseven percent of all Gunnison sagegrouse nests were located less than 6 km
(4 mi) from the lek of capture (Apa
2004, p. 21). While earlier studies
indicated that most greater sage-grouse
hens nest within 3 km (2 mi) of a lek,
more recent research indicated that
many hens actually move much further
from leks to nest based on nesting
habitat quality (Connelly et al. 2004, p.
4-4). Female greater sage-grouse have
been documented to travel more than 20
km (13 mi) to their nest site after mating
(Connelly et al. 2000a, p. 970). Female
Gunnison sage-grouse exhibit strong
fidelity to nesting locations (Young
1994, p. 42; Lyon 2000, p. 20, Connelly
et al. 2004, p. 4-5; Holloran and
Anderson 2005, p. 747). The degree of
fidelity to a specific nesting area
appears to diminish if the female’s first
nest attempt in that area was
unsuccessful (Young 1994, p. 42).
However, there is no statistical
indication that movement to new
nesting areas results in increased
nesting success (Connelly et al. 2004, p.
3-6; Holloran and Anderson 2005, p.
748).
Gunnison sage-grouse typically select
nest sites under sagebrush cover with
some forb and grass cover (Young 1994,
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p. 38), and successful nests were found
in higher shrub density and greater forb
and grass cover than unsuccessful nests
(Young 1994, p. 39). The understory of
productive sage-grouse nesting areas
contains native grasses and forbs, with
horizontal and vertical structural
diversity that provides an insect prey
base, herbaceous forage for pre-laying
and nesting hens, and cover for the hen
while she is incubating (Schroeder et al.
1999, p. 11; Connelly et al. 2000a, p.
971; Connelly et al. 2004, pp. 4-5–4-8).
Shrub canopy and grass cover provide
concealment for sage-grouse nests and
young, and are critical for reproductive
success (Barnett and Crawford 1994, pp.
116-117; Gregg et al. 1994, pp. 164-165;
DeLong et al. 1995, pp. 90-91; Connelly
et al. 2004, p. 4-4). Few herbaceous
plants are growing in April when
nesting begins, so residual herbaceous
cover from the previous growing season
is critical for nest concealment in most
areas (Connelly et al. 2000a, p. 977).
Nesting success for Gunnison sagegrouse is highest in areas where forb
and grass covers are found below a
sagebrush canopy cover of 15 to 30
percent (Young et al. 2000, p. 451).
These numbers are comparable to those
reported for the greater sage-grouse
(Connelly et al. 2000a, p. 971). Nest
success for greater sage-grouse is
greatest where grass cover is present
(Connelly et al. 2000a, p. 971). Because
of the similarities between these two
species, we believe that increased nest
success in areas of forb and grass cover
below the appropriate sagebrush canopy
cover is likely the case for Gunnison
sage-grouse as well.
Mean clutch size for Gunnison sagegrouse is 6.8 ± 0.7 eggs (Young 1994, p.
37). The mean clutch size for Gunnison
sage-grouse in the Gunnison Basin was
6.3, with 94 percent of eggs in
successful nests hatching (Childers
2009, p. 3). Despite average clutch sizes
of 7 eggs (Connelly et al. in press, p. 15),
little evidence exists that populations of
sage-grouse produce large annual
surpluses (Connelly et al. in press, p. 15,
24). The inability of sage-grouse to
produce large annual surpluses limits
their ability to respond under favorable
environmental conditions to make up
for population declines. Re-nesting rates
following the loss of the original nest
appear very low in Gunnison sagegrouse, with one study reporting renesting rates of 4.8 percent (Young
1994, p. 37). Only one instance of renesting was observed over a 5–year
period during which a total of 91
nesting Gunnison sage-grouse hens were
monitored (Childers 2009, p. 3).
Most sage-grouse eggs hatch in June,
with a peak between June 10 and June
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20 (GSRSC, 2005, p. 24). Chicks are
precocial (mobile upon hatching) and
leave the nest with the hen shortly after
hatching. Forbs and insects are essential
nutritional components for sage-grouse
chicks (Klebenow and Gray 1968, pp.
81-83; Peterson 1970, pp. 149-151;
Johnson and Boyce 1991, p. 90;
Connelly et al. 2004, p. 3-3). Therefore,
early brood-rearing habitat for females
with chicks must provide adequate
cover adjacent to areas rich in forbs and
insects to assure chick survival during
this period (Connelly et al. 2000, p. 971;
Connelly et al. 2004, p. 4-11). Gunnison
sage-grouse chick dietary requirements
of insects and forbs also are expected to
be similar to greater sage-grouse and
other grouse species (Apa 2005, pers.
comm.).
The availability of food and cover are
key factors that affect chick and juvenile
survival. During the first 3 weeks after
hatching, insects are the primary food of
chicks (Patterson 1952, p. 201;
Klebenow and Gray 1968, p. 81;
Peterson 1970, pp. 150-151; Johnson
and Boyce 1990, pp. 90-91; Johnson and
Boyce 1991, p. 92; Drut et al. 1994b, p.
93; Pyle and Crawford 1996, p. 320;
Fischer et al. 1996a, p. 194). Diets of 4to 8-week-old greater sage-grouse chicks
were found to have more plant material
as the chicks matured (Peterson 1970, p.
151). Succulent forbs are predominant
in the diet until chicks exceed 3 months
of age, at which time sagebrush becomes
a major dietary component (Klebenow
1969, pp. 665-656; Connelly and
Markham 1983, pp. 171-173; Fischer et
al. 1996b, p. 871; Schroeder et al. 1999,
p. 5).
Early brood-rearing habitat is found
close to nest sites (Connelly et al. 2000a,
p. 971), although individual females
with broods may move large distances
(Connelly 1982, as cited in Connelly et
al. 2000a, p. 971). Young (1994, pp. 4142) found that Gunnison sage-grouse
with broods used areas with lower
slopes than nesting areas, high grass and
forb cover, and relatively low sagebrush
cover and density. Broods frequently
used the edges of hay meadows, but
were often flushed from areas found in
interfaces of wet meadows and habitats
providing more cover, such as sagebrush
or willow-alder (Salix-Alnus).
By late summer and into the early fall,
individuals become more social, and
flocks are more concentrated (Patterson
1952, p. 187). Intermixing of broods and
flocks of adult birds is common, and the
birds move from riparian areas to
sagebrush-dominated landscapes that
continue to provide green forbs. During
this period, Gunnison sage-grouse can
be observed in atypical habitat such as
agricultural fields (Commons 1997, pp.
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79-81). However, broods in the
Gunnison Basin typically do not use hay
meadows further away than 50 meters
(m) (165 feet (ft)) of the edge of
sagebrush stands (Colorado Sage Grouse
Working Group (CSGWG) 1997, p. 13).
As fall approaches, sage-grouse move
from riparian to upland areas and start
to shift to a winter diet (GSRSC 2005,
p. 25). Movements to winter ranges are
slow and meandering (Connelly et al.
1988, p. 119). The extent of movement
varies with severity of winter weather,
topography, and vegetation cover. Sagegrouse may travel short distances or
many miles between seasonal ranges. In
response to severe winters, Gunnison
sage-grouse move as far as 27 km (17 mi)
(Root 2002, p. 14). Flock size in winter
is variable (15 to 100+), and flocks
frequently consist of a single sex (Beck
1977, p. 21).
From late autumn through early
spring, greater and Gunnison sagegrouse diet is almost exclusively
sagebrush (Rasmussen and Griner 1938,
p. 855; Batterson and Morse 1948, p. 20;
Patterson 1952, pp. 197-198; Wallestad
et al. 1975, pp. 628-629; Young et al.
2000, p. 452). Many species of
sagebrush can be consumed (Remington
and Braun 1985, pp. 1056-1057; Welch
et al. 1988, p. 276, 1991; Myers 1992, p.
55). Characteristics of sage-grouse
winter habitats are also similar through
the range of both species (Connelly et al.
2000a, p. 972). In winter, Gunnison
sage-grouse are restricted to areas of 15
to 30 percent sagebrush cover, similar to
the greater sage-grouse (Connelly et al.
2000a, p. 972; Young et al. 2000, p. 451).
However, they may also use areas with
more deciduous shrubs during the
winter (Young et al. 2000, p. 451).
Sagebrush stand selection in winter is
influenced by snow depth (Patterson
1952, pp. 188-189; Connelly 1982 as
cited in Connelly et al. 2000a, p. 980)
and in some areas, topography (Beck
1977, p. 22; Crawford et al. 2004, p. 5).
Winter areas are typically characterized
by canopy cover greater than 25 percent
and sagebrush greater than 30 to 41 cm
(12 to 16 in) tall (Shoenberg 1982, p. 40)
associated with drainages, ridges, or
southwest aspects with slopes less than
15 percent (Beck 1977, p. 22). Lower flat
areas and shorter sagebrush along ridge
tops provide roosting areas. In extreme
winter conditions, greater sage-grouse
will spend nights and portions of the
day burrowed into ‘‘snow burrows’’
(Back et al. 1987, p. 488).
Hupp and Braun (1989, p. 825) found
that most Gunnison sage-grouse feeding
activity in the winter occurred in
drainages and on slopes with south or
west aspects in the Gunnison Basin.
During a severe winter in the Gunnison
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Basin in 1984, less than 10 percent of
the sagebrush was exposed above the
snow and available to sage-grouse
(Hupp, 1987, pp. 45-46). In these
conditions, the tall and vigorous
sagebrush typical in drainages was an
especially important food source.
Sage-grouse typically live between 3
and 6 years, but individuals up to 9
years of age have been recorded in the
wild (Connelly et al. 2004, p. 3-12).
Adult female Gunnison sage-grouse
apparent survival rates from April
through September averaged 57 percent,
and adult male survival averaged 45
percent (Childers 2009, p. 2). From
October through March, adult female
Gunnison sage-grouse apparent survival
rates averaged 79 percent, and adult
male survival averaged 96 percent
(Childers 2009, p.2). In one study,
Gunnison sage-grouse survival from
April 2002 through March 2003 was 48
(± 7) percent for males and 57 (± 7)
percent for females (Apa 2004, p. 22).
Preliminary results from the Gunnison
and San Miguel populations indicate
potential important temporal and spatial
variation in demographic parameters,
with apparent annual adult survival
rates ranging from approximately 65 to
80 percent (CDOW 2009a, p. 8).
Gunnison sage-grouse female survival in
small isolated populations was 52 (± 8)
percent, compared to 71 (± 11) percent
survival in the Gunnison Basin, the only
population with greater than 500
individuals (Apa 2004, p. 22). Higher
adult survival has been observed in a
lower elevation and warmer area (Dry
Creek Basin of the San Miguel
population – 90 percent) than in a
higher elevation and colder, snowier,
area (Miramonte portion of the San
Miguel population – 65 percent) (CDOW
2009a, p.8). Other factors affecting
survival rates include climatic
differences between years and age
(Zablan 1993, pp. 5-6).
Apparent chick survival from hatch to
the beginning of fall (30 September)
averaged 7 percent over a 5–year period
in the western portion of the Gunnison
Basin (Childers 2009, pp. 4-6). Apparent
chick survival to 90 days of age has
ranged from approximately 15 to 30
percent in the Gunnison Basin, with no
juvenile recruitment observed over
several years in the San Miguel
population (CDOW 2009a, p. 8). Based
on a review of many field studies,
juvenile survival rates range from 7 to
60 percent (Connelly et al. 2004, p. 312). The variation in juvenile survival
rates may be associated with sex,
weather, harvest rates (no harvesting of
Gunnison sage-grouse is currently
permitted), age of brood female (broods
with adult females have higher
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survival), and with habitat quality (rates
decrease in poor habitats) (Schroeder et
al. 1999, p. 14; Connelly et al., in press,
p. 20).
Greater sage-grouse require large,
interconnected expanses of sagebrush
with healthy, native understories
(Patterson 1952, p. 9; Knick et al. 2003,
p. 623; Connelly et al. 2004, pp. 4-15;
Connelly et al. in press, p. 10; Pyke in
press, p. 7; Wisdom et al. in press, p. 4).
However, little information is available
regarding minimum sagebrush patch
sizes required to support populations of
greater or Gunnison sage-grouse.
Gunnison sage-grouse have not been
observed to undertake the large seasonal
and annual movements observed in
greater sage-grouse. However,
movements of up to 24 km (15 mi) have
been observed in individual Gunnison
sage-grouse in the Gunnison Basin
population only (Phillips 2010, pers.
comm.).
Sage-grouse typically occupy large
expanses of sagebrush-dominated
habitats composed of a diversity of
sagebrush species and subspecies. Use
of other habitats intermixed with
sagebrush, such as riparian meadows,
agricultural lands, steppe dominated by
native grasses and forbs, scrub willow
(Salix spp.), and sagebrush habitats with
some conifer or quaking aspen (Populus
tremuloides), is not uncommon
(Connelly et al 2004, p. 4-18 and
references therein). Sage-grouse have
been observed using human-altered
habitats throughout their range.
However, the use of non-sagebrush
habitats by sage-grouse is dependent on
the presence of sagebrush habitats in
close proximity (Connelly et a.lal 2004,
p. 4-18 and references therein).
Historic Range and Distribution of
Gunnison Sage-grouse
Based on historical records, museum
specimens, and potential habitat
distribution, Gunnison sage-grouse
historically occurred in southwestern
Colorado, northwestern New Mexico,
northeastern Arizona, and southeastern
Utah (Schroeder et al. 2004, pp. 370371). Accounts of Gunnison sage-grouse
in Kansas and Oklahoma, as suggested
by Young et al. (2000, pp. 446-447), are
not supported with museum specimens,
and Schroeder et al. (2004, p. 371)
found inconsistencies with the
historical records and the sagebrush
habitat currently available in those
areas. Applegate (2001, p. 241) found
that none of the sagebrush species
closely associated with sage-grouse
occurred in Kansas. He attributed
historical, anecdotal reports as mistaken
locations or misidentification of lesser
prairie chickens. For these reasons,
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southwestern Kansas and western
Oklahoma are not considered within the
historic range of Gunnison sage-grouse
(Schroeder et al. 2004, p. 371).
The GSRSC (2005) modified the
historic range from Schroeder et al.
(2004), based on more complete
information on historic and current
habitat and the distribution of the
species (GSRSC 2005, pp. 34-35). Based
on this information, the maximum
Gunnison sage-grouse historical
(presettlement) range is estimated to
have been 55,350 square kilometers
(km2) (21,370 square miles (mi2))
(GSRSC 2005, p. 32). To be clear, only
a portion of the historical range would
have been occupied at any one time,
while all of the current range is
considered occupied. Also, we do not
know what portion of the historical
range was simultaneously occupied, or
what the total population was.
Much of what was once Gunnison
sage-grouse sagebrush habitat was
already lost prior to 1958. A qualitative
decrease in sagebrush was attributed to
overgrazing from the 1870s until about
1934 (Rogers 1964, p. 13). Additional
adverse effects occurred as a result of
newer range management techniques
implemented to support livestock by the
Bureau of Land Management (BLM),
Soil Conservation Service, and U.S.
Forest Service (USFS) (Rogers 1964, p.
13). In the 1950s, large areas of
sagebrush within the range of Gunnison
sage-grouse were eradicated by
herbicide spraying or burning (Rogers
1964, pp. 12-13, 22-23, 26).
About 155,673 hectares (ha) (384,676
ac) of sagebrush habitat was lost from
1958 to 1993 within southwestern
Colorado (Oyler-McCance et al. 2001, p.
327). Sagebrush loss was lower in the
Gunnison Basin (11 percent) compared
to all other areas in southwestern
Colorado (28 percent) (Oyler-McCance
et al. 2001, p. 328). Considerable
fragmentation of sagebrush vegetation
was also quantitatively documented
during that same time period (OylerMcCance et al. 2001, p. 329). Sagegrouse habitat in southwestern Colorado
(the majority of the range of Gunnison
sage-grouse) has been more severely
impacted than sagebrush habitat
elsewhere in Colorado.
The Colorado River Storage Project
(CRSP) resulted in construction of three
reservoirs within the Gunnison Basin in
the mid-late 1960s (Blue Mesa and
Morrow) and mid-1970s (Crystal).
Several projects associated with CRSP
were constructed in this same general
timeframe to provide additional water
storage and resulted in the loss of an
unquantified, but likely small, amount
of sagebrush habitat. These projects
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provide water storage and, to a certain
extent, facilitate agricultural activities
that maintain the fragmentation and
habitat lost historically throughout the
range of Gunnison sage-grouse.
In summary, a substantial amount of
sagebrush habitat within the range of
the Gunnison sage-grouse had been lost
prior to 1960. The majority of the
remaining habitat is highly fragmented,
although to a lesser extent in the
Gunnison Basin than in the remainder
of the species habitat.
Current Distribution and Population
Estimates
The historic and current geographic
ranges of Gunnison’s and greater sagegrouse were quantitatively analyzed to
determine the species’ response to
habitat loss and detrimental land uses
(Wisdom et al., in press, 2009, entire).
A broad spectrum of biotic, abiotic, and
anthropogenic conditions were found to
be significantly different between
extirpated and occupied ranges
(Wisdom et al., in press, 2009, p. 1.).
Sagebrush area is one of the best
landscape predictors of sage-grouse
persistence (Wisdom et al., in press,
2009, p. 17 and references therein).
Because of the loss and fragmentation of
habitat within its range, no expansive,
contiguous areas that could be
considered strongholds (areas of
occupied range where the risk of
extirpation appears low) are evident for
Gunnison sage-grouse (Wisdom et al., in
press, 2009, p. 24). We do not know the
minimum amount of sagebrush habitat
needed by Gunnison sage-grouse to
ensure long-term persistence. However,
based on Wisdom et al., in press, we do
know that landscapes containing large
and contiguous sagebrush patches and
sagebrush patches in close proximity
increase the likelihood of sage-grouse
persistence.
Gunnison sage-grouse currently occur
in seven widely scattered and isolated
populations in Colorado and Utah,
occu2pying 3,795 km2 (1,511mi2)
(GSRSC 2005, pp. 36-37; CDOW 2009b,
p. 1). The seven populations are
Gunnison Basin, San Miguel Basin,
˜
Monticello–Dove Creek, Pınon Mesa,
Crawford, Cerro Summit–Cimarron–
Sims Mesa, and Poncha Pass (Figure 1).
A comparative summary of the land
ownership and recent population
estimates among these seven
populations is presented in Table 1 and
Table 2, respectively. Population trends
over the last nine years indicate that six
of the populations are in decline. The
Gunnison Basin population, while
showing variation over the years, has
been relatively stable through the period
(CDOW 2009a p. 2). Six of the
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populations are very small and
fragmented (all with less than 40,500 ha
(100,000 acres) of habitat likely used by
grouse and less than 50 males counted
on leks) (CDOW 2009a, p. 5). The San
Miguel population, the second largest,
comprises six fragmented
subpopulations.
Figure 1. Locations of Current
Gunnison Sage-grouse Populations.
TABLE 1. PERCENT SURFACE OWNERSHIP OF TOTAL GUNNISON SAGE-GROUSE OCCUPIEDA HABITAT (FROM GSRSCB
2005, PP. D-3-D-6; CDOWC 2009B, P. 1)
Gunnison Sage-grouse Occupied Habitat Management and Ownership
BLMd
USFSf
CDOW
CO
State
Land
Board
State of
UT
Private
%
%
%
%
%
%
acres
592,936
51
2
14
3
<1
0
29
41,022
101,368
36g
0
1
11
3g
0
49g
Monticello–Dove Creek
(Combined)
45,275
111,877
7
0
0
3
0
<1
90
Dove Creek
16,706
41,282
11
0
0
8
0
0
81
Monticello
28,569
70,595
4
0
0
0
0
1
95
˜
Pinon Mesa
15,744
38,904
28
0
2
19
0
0
51
Cerro Summit–Cimarron–
Sims Mesa
15,039
37,161
13
<1
0
11
0
0
76
Crawford
14,170
35,015
63
12
0
2
0
0
23
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239,953
San Miguel Basin
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TABLE 1. PERCENT SURFACE OWNERSHIP OF TOTAL GUNNISON SAGE-GROUSE OCCUPIEDA HABITAT (FROM GSRSCB 2005,
PP. D-3-D-6; CDOWC 2009B, P. 1)—Continued
Gunnison Sage-grouse Occupied Habitat Management and Ownership
Population
hectares
BLMd
NPSe
USFSf
CDOW
CO
State
Land
Board
State of
UT
Private
%
Poncha Pass
acres
%
%
%
%
%
%
8,262
48
0
26
0
2
0
23
379,464
Rangewide
20,415
937,676
42
2
10
5
<1
<1
41
aOccupied
Gunnison sage-grouse habitat is defined as areas of suitable habitat known to be used by Gunnison sage-grouse within the last 10
years from the date of mapping, and areas of suitable habitat contiguous with areas of known use, which have no barriers to grouse movement
from known use areas (GSRSC 2005, p. 54).
bGunnison Sage-grouse Rangewide Steering Committee
cColorado Division of Wildlife
dBureau of Land Management
eNational Park Service
fUnited States Forest Service
gEstimates reported in San Miguel Basin Gunnison Sage-grouse Conservation Plan (2009 p. 28) vary by up to 2 percent in these categories
from those reported here. We consider these differences insignificant.
TABLE 2. GUNNISON SAGE-GROUSE POPULATION ESTIMATES BY YEAR DERIVED FROM THE FORMULA PRESENTED IN THE
GUNNISON SAGE-GROUSE RANGEWIDE CONSERVATION PLAN (GSRSCA 2005, PP. 44-45) APPLIED TO HIGH MALE
COUNTS ON LEKS (CDOWB 2009A, P. 2).
Estimated Population
Year
Population
2001
Gunnison
Basin
2002
2003
2004
2005
2006
2007
2008
2009
2010
3,493
3,027
2,453
2,443
4,700
5,205
4,616
3,669
3,817
3,655
San Miguel
Basin
392
383
250
255
334
378
324
216
162
123
Monticello–
Dove Creek
(Combined)
363
270
186
162
196
191
245
245
191
n/ac
Monticello
231
172
147
152
162
118
216
216
182
n/ac
Dove Creek
132
98
39
10
34
74
29
29
10
44
˜
Pinon Mesa
152
132
123
142
167
152
123
108
78
74
Cerro
Summit–
Cimarron–
Sims Mesa
59
39
29
39
25
49
34
10
39
5
137
206
118
128
191
201
113
103
78
20
25
44
34
39
44
44
25
25
20
15
4,621
4,101
3,194
3,208
5,656
6,220
5,480
4,376
4,386
n/ac
Crawford
Poncha Pass
Totals
aGunnison
Sage-grouse Rangewide Steering Committee
Division of Wildlife
c2010 lek count data for the Monticello group was not available at the time of publication
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bColorado
Gunnison Basin Population – The
Gunnison Basin is an intermontane
basin that includes parts of Gunnison
and Saguache Counties, Colorado. The
current Gunnison Basin population is
distributed across approximately
240,000 ha (593,000 ac), roughly
centered on the town of Gunnison.
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Elevations in the area range from 2,300
to 2,900 m (7,500 to 9,500 ft).
Approximately 70 percent of the land
area is managed by Federal agencies (67
percent) and CDOW (3 percent), and the
remaining 30 percent comprises
primarily private lands. Big sagebrush
(Artemesia tridentata) dominates the
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upland vegetation and has a highly
variable growth form depending on
local site conditions. In 2009, 83 leks
were surveyed for breeding activity in
the Gunnison Basin, and 42 of these leks
were active (at least two males in
attendance during at least two of four
10–day count periods), 6 inactive
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(inactive for at least 5 consecutive
years), 9 historic (inactive for at least 10
consecutive years), and 26 were of
unknown status (variability in counts
resulted in lek not meeting requirements
for active, inactive, or historic) (CDOW
2009d, pp. 28-30). Approximately 45
percent of leks in the Gunnison Basin
occur on private land and 55 percent on
public land, primarily BLM (GSRSC
2005, p. 75). The 2010 population
estimate for the Gunnison Basin was
3,655 (CDOW 2010a, p. 2). Rogers (1964,
p. 20) stated that Gunnison County was
one of five counties containing the
majority of sage-grouse in Colorado in
1961. The vast majority (87 percent) of
Gunnison sage-grouse are now found
only in the Gunnison Basin population.
San Miguel Basin Population – The
San Miguel Basin population is in
Montrose and San Miguel Counties in
Colorado, and is composed of six small
subpopulations using different areas—
(Dry Creek Basin, Hamilton Mesa,
Miramonte Reservoir, Gurley Reservoir,
Beaver Mesa, and Iron Springs)
occupying a total of approximately
41,000 ha (101,000 ac). Some of these
six areas are used year-round by sagegrouse, and others are used seasonally.
The overall acreage figure for this
population is heavily skewed by the
large percentage (approximately 62
percent) of land in the Dry Creek Basin
(San Miguel Basin Gunnison Sagegrouse Working Group 2009, p. 28). The
Dry Creek Basin area contains some of
the poorest habitat and smallest grouse
populations in the San Miguel
population (San Miguel Basin Gunnison
sage-grouse Conservation Plan 2009, pp.
28, 36). Gunnison sage-grouse in the San
Miguel Basin move widely between
these areas (Apa 2004, p. 29; Stiver and
Gibson 2005, p. 12). The area
encompassed by this population is
believed to have once served as critical
migration corridors between
populations to the north (Cerro
Summit–Cimarron–Sims Mesa) and to
the south (Monticello-Dove Creek) (San
Miguel Basin Gunnison Sage-grouse
Working Group 2009, p. 9).
Sagebrush habitat in the Dry Creek
Basin area is patchily distributed, and
the understory is either lacking in grass
and forb diversity or nonexistent. Where
irrigation is possible, private lands in
the southeast portion of Dry Creek Basin
are cultivated. Sagebrush habitat on
private land has been heavily thinned or
removed entirely (GSRSC 2005, p. 96).
Gunnison sage-grouse use the Hamilton
Mesa area (1,940 ha (4,800 ac)) in the
summer, but use of Hamilton Mesa
during other seasons is unknown.
Gunnison sage-grouse occupy
approximately 4,700 ha (11,600 ac)
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around Miramonte Reservoir (GSRSC
2005, p. 96). Sagebrush stands there are
generally contiguous with a mixed grass
and forb understory. Occupied habitat at
the Gurley Reservoir area (3,305 ha
(7,500 ac)) is heavily fragmented by
urban development, and the understory
is a mixed grass and forb community.
Farming attempts in the early 20th
century led to the removal of much of
the sagebrush, although agricultural
activities are now restricted primarily to
the seasonally irrigated crops (hay
meadows), and sagebrush has
reestablished in most of the failed
pastures. However, grazing pressure and
competition from introduced grasses
have kept the overall sagebrush
representation low (GSRSC 2005, pp.
96-97). Sagebrush stands in the Iron
Springs and Beaver Mesa areas (2,590 ha
and 3,560 ha (6,400 ac and 8,800 ac
respectively)) are contiguous with a
mixed grass understory. The Beaver
Mesa area has numerous scattered
patches of oakbrush (Quercus gambelii).
Rogers (1964, p. 9) reported that all big
sagebrush-dominated habitats in San
Miguel and Montrose Counties were
historically used by Gunnison sagegrouse.
The 2010 population estimate for the
entire San Miguel Basin was 123
individuals on nine leks (CDOW 20010,
p. 3). With the exception of 2007,
CDOW has been translocating Gunnison
sage-grouse from the Gunnison Basin to
Dry Creek Basin on a yearly basis since
the spring of 2006 (CDOW 2009a, p.
133). In the spring of 2006, six
individuals were released near the
Desert Lek. An additional two
individuals were released in the fall.
Nine individuals were translocated in
the spring of 2008. An additional 30
individuals were translocated in the fall
of 2009. A 40 to 50 percent mortality
rate has been observed within the first
year after release, compared to an
average annual mortality rate of
approximately 20 percent for
radiomarked adult sage-grouse (CDOWa
2009, p. 9).
Monticello–Dove Creek Population –
This population is divided into two
disjunct subpopulations of Gunnison
sage-grouse. Currently, the largest group
is near the town of Monticello, in San
Juan County, Utah. Gunnison sagegrouse in this subpopulation inhabit a
broad plateau on the northeast side of
the Abajo Mountains, with fragmented
patches of sagebrush interspersed with
large grass pastures and agricultural
fields. The Utah Division of Wildlife
Resources (UDWR) estimated
population numbers between 583 and
1,050 individuals in 1972 and between
178 and 308 individuals in 2002 (UDWR
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2009, 29.21 p. 1). The UDWR estimates
that Gunnison sage-grouse currently
occupy about 24,000 ha (60,000 ac) in
the Monticello area. The 2009
population estimate for Monticello was
182 individuals with three active and
one inactive leks (UDWR 2009, p. 5).
The Dove Creek subpoulation is
located primarily in western Dolores
County, Colorado, north and west of
Dove Creek, although a small portion of
occupied habitat extends north into San
Miguel County. Habitat north of Dove
Creek is characterized as mountain
shrub habitat, dominated by oakbrush
interspersed with sagebrush. The area
west of Dove Creek is dominated by
sagebrush, but the habitat is highly
fragmented. Lek counts in the Dove
Creek area were over 50 males in 1999,
suggesting a population of about 245
birds, but declined to 2 males in 2009
(CDOW 2009a, p. 71), suggesting a
population of 10 birds. A new lek was
found in 2010, and the 2010 population
estimate was 44 individuals on 2 leks
(CDOW 2010, p. 1). Low sagebrush
canopy cover, as well as low grass
height, exacerbated by drought, may
have led to nest failure and subsequent
population declines (Connelly et al.
2000a, p. 974; Apa 2004, p. 30). Rogers
(1964, p. 9) reported that all sagebrushdominated habitats in Dolores and
Montezuma Counties within Gunnison
sage-grouse range in Colorado were
historically used by Gunnison sagegrouse.
˜
˜
Pınon Mesa Population – The Pınon
Mesa population occurs on the
northwest end of the Uncompahgre
Plateau in Mesa County, about 35 km
(22 mi) southwest of Grand Junction,
Colorado. The 2010 population estimate
˜
for Pınon Mesa was 74 (CDOW 2010, p.
2). Of the ten known leks, only four
were active in 2009 (CDOW, 2009a, p.
˜
3). The Pınon Mesa area may have
additional leks, but the high percentage
of private land, a lack of roads, and
heavy snow cover during spring make
locating additional leks difficult.
Gunnison sage-grouse likely occurred
historically in all suitable sagebrush
˜
habitat in the Pınon Mesa area,
including the Dominguez Canyon area
of the Uncompaghre Plateau, southeast
˜
of Pınon Mesa proper (Rogers 1964, p.
114). Their current distribution has been
substantially reduced from historic
levels to 15,744 ha (38,904 ac) (GSRSC
2005, p. 87).
Crawford Population – The Crawford
population of Gunnison sage-grouse is
in Montrose County, Colorado, about 13
km (8 mi) southwest of the town of
Crawford and north of the Gunnison
River. Basin big sagebrush (Artemisia
tridentata tridentata) and black
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sagebrush (A. nova) dominate the midelevation uplands (GSRSC 2005, p. 62).
The 2010 population estimate for
Crawford was 20 individuals (CDOW
2010, p. 1) in 14,170 ha (35,015 ac) of
occupied habitat. Four active leks are
currently in the Crawford population on
BLM lands in sagebrush habitat adjacent
to an 11-km (7-mi) stretch of road. This
area represents the largest contiguous
sagebrush-dominated habitat within the
Crawford boundary (GSRSC 2005, p.
64).
Cerro Summit–Cimarron–Sims Mesa
Population – This population is divided
into two geographically separated
subpopulations, both in Montrose
County, Colorado. The Cerro Summit–
Cimarron subpopulation is centered
about 24 km (15 mi) east of Montrose.
The habitat consists of 15,039 ha
(37,161 ac) of patches of sagebrush
habitat fragmented by oakbrush and
irrigated pastures. Five leks are
currently known in the Cerro Summit–
Cimarron group, but only one
individual was observed on one lek in
2010 resulting in a population estimate
of 5 individuals for the population
(CDOW 2010, p. 1). Rogers (1964, p.
115) noted a small population of sagegrouse in the Cimarron River drainage,
but did not report population numbers.
He noted that lek counts at Cerro
Summit in 1959 listed four individuals.
The Sims Mesa area, about 11 km (7
mi) south of Montrose, consists of small
patches of sagebrush that are heavily
fragmented by pinyon-juniper,
residential and recreational
development, and agriculture. The one
known lek in Sims Mesa has lacked
Gunnison sage-grouse attendance for the
last six years, which indicates this
population is likely extirpated (CDOW
2009a, p. 43). In 2000, the CDOW
translocated six Gunnison sage-grouse
from the Gunnison Basin to Sims Mesa
(Nehring and Apa 2000, p. 12). Rogers
(1964, p. 95) recorded eight males in a
lek count at Sims Mesa in 1960. We do
not know if sage-grouse move between
the Cerro Summit–Cimarron and Sims
Mesa subpopulations.
Poncha Pass Population – The Poncha
Pass Gunnison sage-grouse population
is located in Saguache County,
approximately 16 km (10 mi) northwest
of Villa Grove, Colorado. This
population was established through the
reintroduction of 30 birds from the
Gunnison Basin in 1971 and 1972
during efforts to reintroduce the species
to the San Luis Valley (GSRSC 2005, p.
94). The known population distribution
is in 8,262 ha (20,415 ac) of sagebrush
habitat from the summit of Poncha Pass
extending south for about 13 km (8 mi)
on either side of U.S. Highway 285.
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Sagebrush in this area is continuous
with little fragmentation; sagebrush
habitat quality throughout the area is
adequate to support the species
(Nehring and Apa 2000 p. 25). San Luis
Creek runs through the area, providing
a year-round water source and lush, wet
meadow riparian habitat for broodrearing.
A high male count of 3 males was
made in 2010 (CDOW 2009a, p. 121),
resulting in an estimated population
size of 15 for the Poncha Pass
population (CDOW 2010, p. 3). The only
current lek is located on BLMadministered land. In 1992, a CDOW
effort to simplify hunting restrictions
inadvertently opened the Poncha Pass
area to sage-grouse hunting, and at least
30 grouse were harvested from this
population. Due to declining population
numbers since the 1992 hunt, CDOW
translocated 24 additional birds from
the Gunnison Basin (Nehring and Apa
2000, p. 11). In 2001 and 2002, an
additional 20 and 7 birds, respectively,
were moved to Poncha Pass by the
CDOW (GSRSC 2005, p. 94).
Translocated females have bred
successfully (Apa 2004, pers. comm.),
and display activity resumed on the
historic lek in spring 2001.
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: (1) The
present or threatened destruction,
modification, or curtailment of its
habitat or range; (2) overutilization for
commercial, recreational, scientific, or
educational purposes; (3) disease or
predation; (4) the inadequacy of existing
regulatory mechanisms; or (5) other
natural or manmade factors affecting its
continued existence. In making this
finding, information pertaining to the
Gunnison sage-grouse, in relation to the
five factors provided in section 4(a)(1) of
the Act, is discussed below.
In considering what factors might
constitute threats to a species, we must
look beyond the exposure of the species
to a factor to evaluate whether the
species may respond to the factor in a
way that causes actual impacts to the
species. If there is exposure to a factor
and the species responds negatively, the
factor may be a threat and we attempt
to determine how significant a threat it
is. The threat is significant if it drives,
or contributes to, the risk of extinction
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of the species such that the species
warrants listing as endangered or
threatened as those terms are defined in
the Act.
The Gunnison Basin contains 87
percent of the current rangewide
Gunnison sage-grouse population and
62 percent of the area occupied by the
species. The remaining six populations
cumulatively and individually have
substantially smaller population sizes
and occupy substantially less habitat
than the Gunnison Basin population
(see Table 2).
A. The Present or Threatened
Destruction, Modification, or
Curtailment of Its Habitat or Range
Sagebrush habitats within the range of
Gunnison sage-grouse are becoming
increasingly fragmented as a result of
various changes in land uses and the
expansion in the density and
distribution of invasive plant species
(Oyler-McCance et al. 2001, pp. 329330; Schroeder et al. 2004, p. 372).
Habitat fragmentation is the separation
or splitting apart of previously
contiguous, functional habitat
components of a species. Fragmentation
can result from direct habitat losses that
leave the remaining habitat in noncontiguous patches, or from alteration of
habitat areas that render the altered
patches unusable to a species (i.e.,
functional habitat loss). Functional
habitat losses include disturbances that
change a habitat’s successional state or
remove one or more habitat functions;
physical barriers that preclude use of
otherwise suitable areas; or activities
that prevent animals from using suitable
habitat patches due to behavioral
avoidance.
A variety of human developments
including roads, energy development,
and other factors that cause habitat
fragmentation have contributed to or
been associated with Gunnison and
greater sage-grouse extirpation (Wisdom
et al. in press, p. 18). Based on a
quantitative analysis of environmental
factors most closely associated with
extirpation, no strongholds (areas where
the risk of Gunnison sage-grouse
extirpation is low) exist (Wisdom et al.
in press, p. 26). Estimating the impact
of habitat fragmentation on sage-grouse
is complicated by time lags in response
to habitat changes (Garton et al., in
press, p. 71), particularly since these
relatively long-lived birds will continue
to return to altered breeding areas (leks,
nesting areas, and early brood-rearing
areas) due to strong site fidelity despite
nesting or productivity failures (Rogers
1964, pp. 35-40; Wiens and Rotenberry
1985, p. 666; Young 1994, p. 42; Lyon
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2000, p. 20, Connelly et al. 2004, p. 45;
Holloran and Anderson 2005, p. 747).
Habitat fragmentation can have an
adverse effect on Gunnison sage-grouse
populations. Many of the factors that
result in fragmentation may be
exacerbated by the effects of climate
change, which may influence long-term
habitat and population trends. The
following sections examine factors that
can contribute to habitat fragmentation
to determine whether they threaten
Gunnison sage-grouse and their habitat.
Historic Modification of Gunnison Sagegrouse Habitat
The historic and current distribution
of the Gunnison sage-grouse closely
matches the distribution of sagebrush.
Potential Gunnison sage-grouse range is
estimated to have been 5,536,358 ha
(13,680,640 ac) historically (GSRSC
2005, p. 32). Gunnison sage-grouse
currently occupy approximately 379,464
ha (937,676 ac) in southwestern
Colorado and southeastern Utah (CDOW
2009b, p. 1; GSRSC 2005, p. 81), an area
that represents approximately 7 percent
of the species’ potential historic range.
The following describes the factors
affecting Gunnison sage-grouse and
Gunnison sage-grouse habitat within the
current range of the species.
The onset of EuroAmerican settlement
in the late 1800s resulted in significant
alterations to sagebrush ecosystems
throughout North America (West and
Young 2000, pp. 263-265; Miller et al.
in press, p. 6), primarily as a result of
urbanization, agricultural conversion,
and irrigation projects. Areas that
supported basin big sagebrush
(Artemisia tridentata ssp. tridentata)
were among the first sagebrush
community types converted to
agriculture because their typical soils
and topography are well suited for
agriculture (Rogers 1964, p. 13).
In southwestern Colorado, OylerMcCance et al. (2001, p. 326) found that,
between 1958 and 1993, 20 percent
(155,673 ha (384,676 ac)) of sagebrush
was lost in Colorado, and 37 percent of
sagebrush plots examined were
fragmented. In another analysis, it was
estimated that approximately 342,000
ha (845,000 ac) of sagebrush, or 13
percent of the pre-EuroAmerican
settlement sagebrush extent, were lost in
Colorado, which includes both greater
sage-grouse and Gunnison sage-grouse
habitat (Boyle and Reeder 2005, p. 3-3).
However, the authors noted that the
estimate of historic sagebrush area used
in their analyses was conservative,
possibly resulting in a substantial
underestimate of historic sagebrush
losses (Boyle and Reeder 2005, p. 3-4).
Within the range of Gunnison sage-
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grouse, the principal areas of sagebrush
loss were in the Gunnison Basin, San
Miguel Basin, and areas near Dove
Creek, Colorado. The authors point out
that the rate of loss in the Gunnison
Basin was lower than other areas of
sagebrush distribution in Colorado. The
Gunnison Basin contains approximately
250,000 ha (617,000 ac) of sagebrush;
this area partially comprises other
habitat types such as riparian areas and
patches of non-sagebrush vegetation
types, including aspen forest, mixedconifer forest, and oakbrush (Boyle and
Reeder 2005, p. 3-3). Within the portion
of the Gunnison Basin currently
occupied by Gunnison sage-grouse,
170,000 ha (420,000 ac) comprises
exclusively sagebrush vegetation types,
as derived from Southwest Regional Gap
Analsis Project (SWReGAP) landcover
data (multi-season satellite imagery
acquired between 1999 and 2001)
(USGS 2004, entire).
Conversion to Agriculture
While sage-grouse may forage on
agricultural croplands, they avoid
landscapes dominated by agriculture
(Aldridge et al. 2008, p. 991). Influences
resulting from agricultural activities
extend into adjoining sagebrush, and
include increased predation and
reduced nest success due to predators
associated with agriculture (Connelly et
al. 2004, p. 7-23). Agricultural
conversion can provide some limited
benefits for sage-grouse. Some crops,
such as alfalfa (Medicago sativa) and
young bean sprouts (Phaseolus spp.),
are eaten or used for cover by Gunnison
sage-grouse (Braun 1998, pers. comm.).
However, crop monocultures do not
provide adequate year-round food or
cover (GSRSC 2005, pp. 22-30).
Current Agriculture in All Gunnison
Sage-grouse Population Areas – The
following estimates of land area
dedicated to agriculture (including
grass/forb pasture) were derived from
SWReGAP landcover data (USGS 2004,
entire). Habitat conversion to agriculture
is most prevalent in the Monticello–
Dove Creek population area where
approximately 23,220 ha (57,377 ac) or
51 percent of Gunnison sage-grouse
occupied range is currently in
agricultural production. In the
Gunnison Basin, approximately 20,754
ha (51,285 ac) or 9 percent of the
occupied range is currently in
agricultural production. Approximately
6,287 ha (15,535 ac) or 15 percent of the
occupied range in the San Miguel Basin
is currently in agricultural production.
In the Cerro Summit–Cimarron–Sims
Mesa population, approximately 14
percent (5,133 ha (2,077 ac)) of the
occupied range is currently in
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agricultural production. Habitat
conversion due to agricultural activities
˜
is limited in the Crawford, Pınon Mesa,
and Poncha Pass populations, with 3
percent or less of the occupied range
currently in agricultural production in
each of the population areas.
Other than in Gunnison County, total
area of harvested cropland has declined
over the past two decades in all counties
within the occupied range of Gunnison
sage-grouse (USDA NASS 2010, entire).
Information on the amount of land area
devoted to cropland was not available
for Gunnison County, most likely
because the majority of agricultural land
use in the county is for hay production.
However, total area in hay production
has correspondingly declined in
Gunnison County over the past two
decades (USDA NASS 2009, p. 1).
Because of this long-term trend in
reduced land area devoted to
agriculture, we do not expect a
significant amount of Gunnison sagegrouse habitat to be converted to
agricultural purposes in the future.
Conservation Reserve Program – The
loss of Gunnison sage-grouse habitat to
conversion to agriculture has been
mitigated somewhat by the
Conservation Reserve Program (CRP).
The CRP is administered by the United
States Department of Agriculture
(USDA) Farm Service Agency (FSA) and
provides incentives to agricultural
landowners to convert certain cropland
to more natural vegetative conditions.
Except in emergency situations, CRPenrolled lands are not hayed or grazed.
Lands within the occupied range of
Gunnison sage-grouse enrolled into the
CRP are limited to Dolores and San
Miguel counties in Colorado, and San
Juan County in Utah (USDA FSA 2010,
entire). From 2000 to 2008, CRPenrollment averaged 10,622 ha (26,247
ac) in Dolores County, 1,350 ha (3,337
ac) in San Miguel County, and 14,698 ha
(36,320 ac) in San Juan County (USDA
FSA 2010, entire). These CRP enrolled
areas potentially constitute
approximately 56 percent of the
Monticello–Dove Creek population and
3 percent of the San Miguel population;
however, we are unsure of the
proportion of these CRP lands that are
within Gunnison sage-grouse habitat.
Approximately 735 ha (1,816 ac) of
leases on these CRP-enrolled lands
expired on September 30, 2009, and
10,431 ha (25,778 ac) are due to expire
on September 30, 2010 (UDWR 2009, p.
7).
In San Juan County, Gunnison sagegrouse use CRP lands in proportion to
their availability (Lupis et al. 2006, p.
959). The CRP areas are used by grouse
primarily as brood-rearing habitat, but
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these areas vary greatly in plant
diversity and forb abundance, and
generally lack any shrub cover (Lupis et
al. 2006, pp. 959-960). In response to a
severe drought, four CRP parcels
totaling 1,487 ha (3,674 ac) in San Juan
County, UT, were emergency grazed for
a duration of 1 to 2 months in the
summer of 2002 (Lupis 2006, p. 959).
Largely as a result of agricultural
conversion, sagebrush patches in the
Monticello–Dove Creek subpopulation
area have progressively become smaller
and more fragmented, which has limited
the amount of available nesting and
winter habitat (GSRSC 2005, pp. 82,
276). Overall, the CRP has protected a
portion of the Monticello–Dove Creek
population from more intensive
agricultural use and development.
However, the overall value of CRP lands
is limited because they largely lack
sagebrush cover required by Gunnison
sage-sage grouse throughout most of the
year. The CRP was renewed under the
Food, Conservation, and Energy Act of
2008. A new CRP sign-up for individual
landowners is not anticipated until 2012
and the extent to which existing CRP
lands will be re-enrolled is unknown
(UDWR 2009, p. 4).
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Summary of Conversion to Agriculture
Throughout the range of Gunnison
sage-grouse there is a declining trend in
the amount of land area devoted to
agriculture. Therefore, although we
expect a large proportion of land
currently in agricultural production to
remain so indefinitely, we do not expect
significant additional, future habitat
conversion to agriculture within the
range of Gunnison sage-grouse. The loss
of sagebrush habitat from 1958 to 1993
was estimated to be approximately 20
percent throughout the range of
Gunnison sage-grouse (Oyler-McCance
et al. 2001, p. 326). The exception is the
Monticello–Dove Creek population
where more than half of the occupied
range is currently in agriculture or other
land uses incompatible with Gunnison
sage-grouse conservation. This habitat
loss is being somewhat mitigated by the
current enrollment of lands in the CRP.
Even so, this relative scarcity of
sagebrush cover indicates a high risk of
population extirpation (Wisdom et al. in
press, p. 19) for this population.
Because of its limited extent, we do not
consider the conversion of sagebrush
habitats to agriculture alone to be a
current or future significant threat to
Gunnison sage-grouse and its habitat.
However, we recognize lands already
converted to agriculture are located
throughout all Gunnison sage-grouse
populations and are, therefore,
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contributing to the fragmentation of
remaining habitat.
Water Development
Water Development in All Population
Areas – Irrigation projects have resulted
in loss of sage-grouse habitat (Braun
1998, p. 6). Reservoir development in
the Gunnison Basin flooded 3,700 ha
(9,200 ac), or 1.5 percent of likely sagegrouse habitat (McCall 2005, pers.
comm.). Three other reservoirs
inundated approximately 2 percent of
habitat in the San Miguel Basin
population area (Garner 2005, pers.
comm.). We are unaware of any plans
for additional reservoir construction.
Because of the small amount of
Gunnison sage-grouse habitat lost to
water development projects and the
unlikelihood of future projects, we do
not consider water development alone
to be a current or future significant
threat to the Gunnison sage-grouse.
However, we expect these existing
reservoirs to be maintained indefinitely,
thus acting as another source of
fragmentation of Gunnison sage-grouse
habitat.
Residential Development
Human population growth in the rural
Rocky Mountains is driven by the
availability of natural amenities,
recreational opportunities, aesthetically
desirable settings, grandiose
viewscapes, and perceived remoteness
(Riebsame 1996, p. 396, 402; Theobald
1996, p. 408; Gosnell and Travis 2005,
pp. 192-197; Mitchell et al. 2002, p. 6;
Hansen et al. 2005, pp. 1899-1901). This
human population growth is occurring
throughout much of the range of
Gunnison sage-grouse. The human
population in all counties within the
range of Gunnison sage-grouse averaged
a 70 percent increase since 1980
(Colorado Department of Local Affairs
(CDOLA) 2009a, pp. 2-3). The year 2050
projected human population for the
Gunnison River basin (an area that
encompasses the majority of the current
range of Gunnison sage-grouse) is
expected to be 2.3 times greater than the
2005 population (CWCB 2009, p. 15).
The population of Gunnison County, an
area that supports over 80 percent of all
Gunnison sage-grouse, is predicted to
more than double to approximately
31,100 residents by 2050 (CWCB 2009,
p. 53).
The increase in residential and
commercial development associated
with the expanding human population
is different from historic land use
patterns (Theobald 2001, p. 548). The
allocation of land for resource-based
activities such as agriculture and
livestock production is decreasing as the
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relative economic importance of these
activities diminishes (Theobald 1996, p.
413; Sammons 1998, p. 32; Gosnell and
Travis 2005, pp. 191-192). Currently,
agribusiness occupations constitute
approximately 3 percent of the total job
base in Gunnison County (CDOLAb
2009, p. 4). Recent conversion of farm
and ranch lands to housing
development has been significant in
Colorado (Odell and Knight 2001, p.
1144). Many large private ranches in the
Rocky Mountains, including the
Gunnison Basin, are being subdivided
into both high-density subdivisions and
larger, scattered ranchettes with lots
typically greater than 14 ha (35 ac),
which encompass a large, isolated house
(Riebsame 1996, p. 399; Theobald 1996,
p. 408).
The resulting pattern of residential
development is less associated with
existing town sites or existing
subdivisions, and is increasingly
exurban in nature (Theobald et al. 1996,
pp. 408, 415; Theobald 2001, p. 546).
Exurban development is described as
low-density growth outside of urban
and suburban areas (Clark et al. 2009, p.
178; Theobald 2004, p.140) with less
than one housing unit per 1 ha (2.5 ac)
(Theobald 2003, p. 1627; Theobald
2004, p. 139). The resulting pattern is
one of increased residential lot size and
the diffuse scattering of residential lots
in previously rural areas with a
premium placed on adjacency to federal
lands and isolated open spaces
(Riebsame et al. 1996, p. 396, 398;
Theobald 1996, pp. 413, 417; Theobald
2001, p. 546; Brown et al. 2005, p.
1858). The residential subdivision that
results from exurban development
causes landscape fragmentation (Gosnell
and Travis 2005, p. 196) primarily
through the accumulation of roads,
buildings, (Theobald 1996, p. 410;
Mitchell et al. 2002, p. 3) and other
associated infrastructure such as power
lines, and pipelines. In the East River
Valley of Gunnison County, residential
development in the early 1990s
increased road density by 17 percent
(Theobald et al. 1996, p. 410). The
habitat fragmentation resulting from this
development pattern is especially
detrimental to Gunnison sage-grouse
because of their dependence on large
areas of contiguous sagebrush (Patterson
1952, p. 48; Connelly et al. 2004, p. 41; Connelly et al. in press a, p. 10;
Wisdom et al. in press, p. 4).
Residential Development in the
Gunnison Basin Population Area –
Nearly three quarters (approximately 71
percent) of the Gunnison Basin
population of Gunnison sage-grouse
occurs within Gunnison County, with
the remainder occurring in Saguache
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County. Within Gunnison County,
approximately 30 percent of the
occupied range of this species occurs on
private lands. We performed a GIS
analysis of parcel ownership data that
was focused on the spatial and temporal
pattern of human development within
occupied Gunnison sage-grouse habitat.
Some of our analyses were limited to
the portion of occupied habitat in
Gunnison County because parcel data
was only available for Gunnison County
and not for Saguache County. The
cumulative number of human
developments has increased
dramatically in Gunnison County,
especially since the early 1970s
(USFWS 2010a, p. 1). The number of
new developments averaged
approximately 70 per year from the late
1800s to 1969, increasing to
approximately 450 per year from 1970
to 2008 (USFWS 2010a, pp. 2-5).
Furthermore, there has been an
increasing trend toward development
away from major roadways (primary and
secondary paved roads) into areas that
had previously undergone very limited
development in occupied Gunnison
sage-grouse habitat (USFWS 2010b, p.
7). Between 1889 and 1968, there were
approximately 51 human developments
located more than 1.6 km (1 mi) from a
major road in currently occupied
Gunnison sage-grouse habitat. Between
1969 and 2008, this number increased to
approximately 476 developments
(USFWS 2010b, p. 7).
In order to assess the impacts of
existing residential development, we
relied on two evaluations of Gunnison
sage-grouse response and habitat
availability in relation to development.
The first was a landscape-scale spatial
model predicting Gunnison sage-grouse
nesting probability in the Gunnison
Basin (Aldridge et al. 2010, entire). The
model indicated that Gunnison sagegrouse select nest sites in areas with
moderate shrub cover, and avoid
residential development within a radius
of 1.5 km (0.9 mi) (Aldridge et al. 2010,
p. 18). The model was applied to the
entire Gunnison Basin population area
to predict the likelihood of Gunnison
sage-grouse nesting based on data from
the western portion (Aldridge et al.
2010, p. 16). We used Aldridge et al.
(2010)’s radius of 1.5 km (0.9 mi)
avoidance distance to calculate the
indirect effects likely from the current
level of development within occupied
Gunnison sage-grouse habitat in
Gunnison County. We found that 49
percent of the land area within the range
of Gunnison sage-grouse has at least one
housing unit within a radius of 1.5 km
(0.9 mi) (USFWS 2010b, p. 7). This
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residential development is currently
compromising the likelihood of use by
Gunnison sage-grouse for nesting habitat
in these areas.
Furthermore, since early broodrearing habitat is often in close
proximity to nest sites (Connelly et al.
2000a, p. 971), the functional loss of
nesting habitat is closely linked with the
loss of early brood-rearing habitat.
Limitations in the quality and quantity
of nesting and early brood-rearing
habitat are particularly problematic
because Gunnison sage-grouse
population dynamics are most sensitive
during these life-history stages (GSRSC
2005, p. G-15). We recognize that the
potential percentages of habitat loss
mentioned above, whether direct or
functional, will not necessarily
correspond to the same percentage loss
in sage-grouse numbers. The recent
efforts to conserve Gunnison sagegrouse and their habitat within the
Basin provide protection for the
foreseeable future for several areas of
high-quality habitat (see discussion in
Factor D). Nonetheless, given the large
landscape-level needs of this species,
we expect this current level of habitat
loss, degradation, and fragmentation,
from residential development, as
described above, to substantially limit
the probability of persistence of
Gunnison sage-grouse in the Gunnison
Basin.
We also calculated a ‘‘lower’’
development impact scenario using the
smaller impact footprint hypothesized
by the GSRSC (2005, pp. 160-161). This
analysis assumed that residential
density in excess of one housing unit
per 1.3 km2 (0.5 mi2) could cause
declines in Gunnison sage-grouse
populations. Within Gunnison County,
18 percent of the land area within the
range of Gunnison sage-grouse currently
has a residential density greater than
one housing unit per 1.3 km2 (0.5 mi2)
(USFWS 2010b, p. 8). Therefore,
according to the GSRSC estimate of
potential residential impacts, human
residential densities in the Gunnison
Basin population area are such that we
expect they are limiting the Gunnison
sage-grouse population in at least 18
percent of the population area.
We expect the density and
distribution of human residences to
expand in the future. Based on our GIS
analysis, we estimate that
approximately 20,236 ha (50,004 ac) of
private lands on approximately 1,190
parcels not subject to conservation
easements currently lack human
development in occupied Gunnison
sage-grouse habitat in Gunnison County
(USFWS 2010b, p. 11). These lands are
scattered throughout occupied
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Gunnison sage-grouse habitat in the
Gunnison Basin. We used the 20,236 ha
(50,004 ac) as an initial basis to assess
the potential impacts of future
development. A lack of parcel data
availability from surrounding counties
precluded expanding this analysis
beyond Gunnison County; however, the
analysis area constitutes 71 percent of
the Gunnison Basin population area.
Approximately 93 percent of occupied
Gunnison sage-grouse habitat in
Gunnison County consists of parcels
greater than 14.2 ha (35 ac), allowing
exemptions from some county land
development regulations. Applying a
1.7 percent average annual population
increase under a ‘‘middle’’ growth
scenario (CWCB 2009, p. 56) and an
average 2.29 persons per household
(CDOLA 2009b, p. 6) to the 2008
Gunnison County human population
estimate results in the potential addition
of nearly 7,000 housing units to the
county by 2050.
Currently, approximately two-thirds
of the human population in Gunnison
County occurs within the currently
mapped occupied range of Gunnison
sage-grouse. Assuming this pattern will
continue, two-thirds of the population
increase will occur within occupied
Gunnison sage-grouse habitat. The
above projection could potentially result
in the addition of approximately 4,630
housing units and the potential for
25,829 ha (63,824 ac) of new habitat
loss, whether direct or functional, on
parcels that currently have no
development. Based on the estimated
area of impact determined by Aldridge
et al. (2010), this potential functional
habitat loss constitutes an additional
impact of 15 percent of the current
extent of the Gunnison Basin population
area (USFWS 2010b, p. 14). When
combined with the existing loss,
whether direct or functional, of 49
percent of Gunnison sage-grouse nesting
habitat, the total amount of habitat
subject to the indirect effects of
residential development now and in the
foreseeable future increases to 64
percent.
Using the same methodology as
discussed above, but applying the
estimated area of impact determined by
GSRSC (2005, p. F-3), results in a future
potential functional habitat loss of 9
percent. When combined with the
existing loss, whether direct or
functional, of 18 percent of Gunnison
sage-grouse habitat, an estimated 27
percent of habitat will be functionally
lost for Gunnison sage-grouse under this
minimum impact scenario. We believe
that impacts to Gunnison sage-grouse
implicit in even the lower or more
conservative estimates of direct and
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functional habitat loss are limiting the
persistence of the species.
We also anticipate increased housing
density in many areas of occupied
Gunnison sage-grouse habitat because
the anticipated number of new housing
units will exceed the number of
undeveloped parcels by nearly four
times (USFWS 2010b, p. 16). Some of
this anticipated development and
subsequent functional habitat loss will
undoubtedly occur on parcels that
currently have existing human
development, which could lessen the
effects to Gunnison sage-grouse.
However, the above calculation of an
increase in future housing units is likely
an underestimate because it does not
take into account the expected increase
in second home development (CDOLA
2009b, p. 7), which could increase
negative effects to Gunnison sagegrouse. The U.S. Census Bureau only
tallies the inhabitants of primary
residences in population totals. This
methodology results in an
underestimate of the population,
particularly in amenity communities,
because of the increased number of parttime residents inhabiting second homes
and vacation homes in these areas
(Riebsame 1996, p. 397; Theobald 2001,
p. 550, Theobald 2004, p. 143). In
Gunnison County, approximately 90
percent of vacant housing units were
seasonal-use units (CDOLA 2009c, p. 1).
The housing vacancy rate, which is
computed by dividing the number of
vacant housing units by the total
housing units, was 42.5 percent in
Gunnison County over the last two
decades (CDOLA 2009d, p. 2).
We expect some development to be
moderated by the establishment of
additional voluntary landowner
conservation easements such as those
currently facilitated by the CDOW and
land trust organizations. While
conservation easements can minimize
the overall impacts to Gunnison sagegrouse, because less than 5 percent of
occupied Gunnison sage-grouse habitat
in the Gunnison Basin has been placed
in conservation easements to date, we
do not expect the amount of land
potentially placed in future easements
will significantly offset the overall
affects of human development.
Our analyses, based on the
evaluations of impacts to Gunnison
sage-grouse discussed above, result in
estimates of existing functional habitat
loss of 18 to 49 percent of the Gunnison
Basin population area. Future estimates
of functional habitat loss result in an
increase of 9 to 15 percent, for a
cumulative total of 27 and 64 percent
loss of the Gunnison Basin population
area. We believe that impacts within
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these ranges limit the persistence of
Gunnison sage-grouse.
Residential Development in All Other
Population Areas – In 2004, within the
Crawford Population area,
approximately 951 ha (2,350 ac), or 7
percent of the occupied Gunnison sagegrouse habitat, was subdivided into 48
parcels ranging in size from 14.2 ha (35
ac) to 28.3 ha (70 ac) (CDOW 2009a, p.
59). Local landowners and the National
Park Service (NPS) have ongoing efforts
to protect portions of the subdivided
area through conservation easements.
Residential subdivision continues to
occur in the northern part of the Poncha
Pass population area, and the CDOW
considers this to be the highest priority
threat to this population (CDOW 2009a,
p. 124). The rate of residential
development in the San Miguel Basin
population increased between 2005 and
2008 but slowed in 2009 (CDOW 2009a,
p. 135). However, a 429 ha (1,057 ac)
parcel north of Miramonte Reservoir is
currently being developed as a retreat.
The CDOW reports that potential
impacts to Gunnison sage-grouse
resulting from the development may be
reduced by possibly placing a portion of
the property into a conservation
easement and the relocation of a
proposed major road to avoid occupied
habitat (CDOW 2009a, p. 136). No recent
or planned residential developments are
known for the Cerro Summit–Cimarron–
Sims Mesa population area (CDOW
2009a, p. 45), Monticello–Dove Creek
population area (CDOW 2009a, p. 73), or
˜
Pınon Mesa population area (CDOW
2009a, p. 109). The remaining limited
amounts of habitat, the fragmented
nature of this remaining habitat, and the
anticipated increases in exurban
development within each of the six
smaller populations pose a significant
threat to these six populations.
Summary of Residential Development
Because Gunnison sage-grouse are
dependent on expansive, contiguous
areas of sagebrush habitat to meet their
life-history needs, the development
patterns described above have resulted
in the direct and functional loss of
sagebrush habitat and have negatively
affected the species by limiting already
scarce habitat, especially within the six
smaller populations. The collective
influences of fragmentation and
disturbance from human activities
around residences and associated roads
reduce the effective habitat around these
areas, making them inhospitable to
Gunnison sage-grouse (Aldridge et al.
2010, pp. 24-25; Knick, et al. 2009, in
press, p. 25 and references therein;
Aldridge and Boyce 2007, p.520).
Human population growth that results
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in a dispersed exurban development
pattern throughout sagebrush habitats
will reduce the likelihood of sage-grouse
persistence in these areas. Human
populations are increasing throughout
the range of Gunnison sage-grouse, and
we expect this trend to continue. Given
the current demographic trends
described above, we believe the rate of
residential development in Gunnison
sage-grouse habitat will continue at least
through 2050, and likely longer. The
resulting habitat loss and fragmentation
from residential development is a
significant threat to Gunnison sagegrouse now and in the foreseeable
future.
Fences
The effects of fencing on sage-grouse
include direct mortality through
collisions, creation of raptor and corvid
(Family Corvidae: crows, ravens,
magpies, etc.) perch sites, the potential
creation of predator corridors along
fences (particularly if a road is
maintained next to the fence), incursion
of exotic species along the fencing
corridor, and habitat fragmentation (Call
and Maser 1985, p. 22; Braun 1998, p.
145; Connelly et al. 2000a, p. 974; Beck
et al. 2003, p. 211; Knick et al. 2003, p.
612; Connelly et al. 2004, p. 1-2).
Corvids are significant sage-grouse nest
predators and were responsible for more
than 50 percent of nest predations in
Nevada (Coates 2007, pp. 26-30). Sagegrouse frequently fly low and fast across
sagebrush flats, and fences can create a
collision hazard resulting in direct
mortality (Call and Maser 1985, p. 22).
Not all fences present the same
mortality risk to sage-grouse. Mortality
risk appears to be dependent on a
combination of factors including design
of fencing, landscape topography, and
spatial relationship with seasonal
habitats (Christiansen 2009). This
variability in fence mortality rate and
the lack of systematic fence monitoring
make it difficult to determine the
magnitude of impacts to sage-grouse
populations; however, in some cases the
level of mortality is likely significant to
localized areas within populations.
Fences directly kill greater sage grouse
(Call and Maser 1985, p. 22;
Christiansen 2009, pp. 1-2); we assume
that Gunnison sage-grouse are also
killed by fences but do not have speciesspecific data. Although the effects of
direct strike mortality on populations
are not fully analyzed, fences are
ubiquitous across the landscape. Fence
collisions continue to be identified as a
source of mortality for Gunnison and
greater sage-grouse and we expect this
source of mortality to continue into the
foreseeable future (Braun 1998, p. 145;
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Connelly et al. 2000a, p. 974; OylerMcCance et al. 2001, p. 330; Connelly et
al. 2004, p. 7-3).
Fence posts create perching places for
raptors and corvids, which may increase
their ability to prey on sage-grouse
(Braun 1998, p. 145; Oyler-McCance et
al. 2001, p. 330; Connelly et al. 2004, p.
13-12). We anticipate that the effect on
sage-grouse populations through the
creation of new raptor perches and
predator corridors into sagebrush
habitats is similar to that of powerlines
discussed below (Braun 1998, p. 145;
Connelly et al. 2004, p. 7-3). Fences and
their associated roads also facilitate the
spread of invasive plant species that
replace sagebrush plants upon which
sage-grouse depend (Braun 1998, p. 145;
Connelly et al. 2000a, p. 973; Gelbard
and Belnap 2003, p. 421; Connelly et al.
2004, p. 7-3). Greater sage-grouse
avoidance of habitat adjacent to fences,
presumably to minimize the risk of
predation, effectively results in habitat
fragmentation even if the actual habitat
is not removed (Braun 1998, p. 145).
Because of similarities in behavior and
habitat use, we believe the response of
Gunnison sage-grouse is similar to that
observed in greater sage-grouse.
At least 1,540 km (960 mi) of fence are
on BLM lands within the Gunnison
Basin (Borthwick 2005a, pers. comm.;
BLM 2005a, 2005e) and an unquantified
amount of fence on land owned or
managed by other landowners. Fences
are present within all other Gunnison
sage-grouse population areas, but we
have no quantitative information on the
amount or types of fencing in these
areas.
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Summary of Fences
While fences contribute to habitat
fragmentation and increase the potential
for loss of individual grouse through
collisions or enhanced predation, such
effects have been ongoing since the first
agricultural conversions occurred in
sage-grouse habitat. We expect that the
majority of existing fences will remain
on the landscape indefinitely. However,
because we do not expect a major
increase in the number of fences,
particularly 3-wire range fencing, we do
not believe fencing, on its own, is a
significant threat to Gunnison sagegrouse at the species level. In the
smaller Gunnison sage-grouse
populations, the impacts of fencing
could become another source of
mortality that cumulatively affects the
species. We also recognize that fences
are located throughout all Gunnison
sage-grouse populations and are,
therefore, contributing to the
fragmentation of remaining habitat.
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Roads
Impacts from roads may include
direct habitat loss, direct mortality,
barriers to migration corridors or
seasonal habitats, facilitation of
predation and spread of invasive
vegetative species, and other indirect
influences such as noise (Forman and
Alexander 1998, pp. 207-231). Greater
sage-grouse mortality resulting from
collisions with vehicles does occur, but
mortalities are typically not monitored
or recorded (Patterson 1952, p. 81).
Therefore, we are unable to determine
the importance of this factor on sagegrouse populations. We have no
information on the number of direct
mortalities of Gunnison sage-grouse
resulting from vehicles or roads;
however, because of similarities in their
habitat and habitat use, we expect
similar effects as those observed in
greater sage-grouse. Roads within
Gunnison sage-grouse habitats have
been shown to impede movement of
local populations between the resultant
patches, with road avoidance
presumably being a behavioral means to
limit exposure to predation (OylerMcCance et al. 2001, p. 330).
The presence of roads increases
human access and resulting disturbance
effects in remote areas (Forman and
Alexander 1998, p. 221; Forman 2000,
p. 35; Connelly et al. 2004, pp. 7-6 to
7-25). In addition, roads can provide
corridors for predators to move into
previously unoccupied areas. For some
mammalian species known to prey on
sage-grouse, such as red fox (Vulpes
vulpes), raccoons (Procyon lotor), and
striped skunks (Mephitis mephitis),
dispersal along roads has greatly
increased their distribution (Forman
and Alexander 1998, p. 212; Forman
2000, p. 33; Frey and Conover 2006, pp.
1114-1115). Corvids also use linear
features such as primary and secondary
roads as travel routes, expanding their
movements into previously unused
regions (Knight and Kawashima 1993, p.
268; Connelly et al. 2004, p. 12-3).
Corvids are significant sage-grouse nest
predators and were responsible for more
than 50 percent of nest predations in
Nevada (Coates 2007, pp. 26-30). Ravens
were documented following roads in oil
and gas fields while foraging (Bui 2009,
p. 31).
The expansion of road networks
contributes to exotic plant invasions via
introduced road fill, vehicle transport,
and road maintenance activities
(Forman and Alexander 1998, p. 210;
Forman 2000, p. 32; Gelbard and Belnap
2003, p. 426; Knick et al. 2003, p. 619;
Connelly et al. 2004, p. 7-25). Invasive
species are not limited to roadsides, but
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also encroach into surrounding habitats
(Forman and Alexander 1998, p. 210;
Forman 2000, p. 33; Gelbard and Belnap
2003, p. 427). In their study of roads on
the Colorado Plateau of southern Utah,
Gelbard and Belnap (2003, p. 426) found
that improving unpaved four-wheel
drive roads to paved roads resulted in
increased cover of exotic plant species
within the interior of adjacent plant
communities. This effect was associated
with road construction and maintenance
activities and vehicle traffic, and not
with differences in site characteristics.
The incursion of exotic plants into
native sagebrush systems can negatively
affect Gunnison sage-grouse through
habitat losses and conversions (see
further discussion below in Invasive
Plants).
Additional indirect effects of roads
may result from birds’ behavioral
avoidance of road areas because of
noise, visual disturbance, pollutants,
and predators moving along a road. The
landscape-scale spatial model
predicting Gunnison sage-grouse nest
site selection showed strong avoidance
of areas with high road densities of
roads classed 1 through 4 (primary
paved highways through primitive roads
with 2-wheel drive sedan clearance)
within 6.4 km (4 mi)) of nest sites
(Aldridge et al. 2010 p. 18). The
occurrence of Gunnison sage-grouse
nest sites also decreased with increased
proximity to primary and secondary
paved highways (roads classes 1 and 2)
(Aldridge et al. 2010, p. 27). Male
greater sage-grouse lek attendance was
shown to decline within 3 km (1.9 mi)
of a methane well or haul road with
traffic volume exceeding one vehicle per
day (Holloran 2005, p. 40). Male sagegrouse depend on acoustical signals to
attract females to leks (Gibson and
Bradbury 1985, p. 82; Gratson 1993, p.
692). If noise interferes with mating
displays, and thereby female
attendance, younger males will not be
drawn to the lek and eventually leks
will become inactive (Amstrup and
Phillips 1977, p. 26; Braun 1986, pp.
229-230).
In a study on the Pinedale Anticline
in Wyoming, greater sage-grouse hens
that bred on leks within 3 km (1.9 mi)
of roads associated with oil and gas
development traveled twice as far to
nest as did hens that bred on leks
greater than 3 km (1.9 mi) from roads.
Nest initiation rates for hens bred on
leks close to roads also were lower (65
versus 89 percent), affecting population
recruitment (33 versus 44 percent)
(Lyon 2000, p. 33; Lyon and Anderson
2003, pp. 489-490). Lyon and Anderson
(2003, p. 490) suggested that roads may
be the primary impact of oil and gas
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development to sage-grouse, due to their
persistence and continued use even
after drilling and production have
ceased. Lek abandonment patterns
suggested that daily vehicular traffic
along road networks for oil wells can
impact greater sage-grouse breeding
activities (Braun et al. 2002, p. 5). We
believe the effects of vehicular traffic on
Gunnison sage-grouse, regardless of its
purpose (e.g., in support of energy
production or local commuting and
recreation), are similar to those observed
in greater sage-grouse.
Aldridge et al. (2008, p. 992) did not
find road density to be an important
factor affecting greater sage-grouse
persistence or rangewide patterns in
sage-grouse extirpation. However, the
authors did not consider the intensity of
human use of roads in their modeling
efforts. They also indicated that their
analyses may have been influenced by
inaccuracies in spatial road data sets,
particularly for secondary roads
(Aldridge et al. 2008, p. 992). Historic
range where greater and Gunnison sage
grouse have been extirpated has a 25
percent higher density of roads than
occupied range (Wisdom et al. in press,
p. 18). Wisdom et al.’s (in press) greater
and Gunnison sage-grouse rangewide
analysis supports the findings of
numerous local studies showing that
roads can have both direct and indirect
impacts on sage-grouse distribution and
individual fitness (reproduction and
survival) (e.g., Lyon and Anderson 2003
p. 490 , Aldridge and Boyce 2007, p.
520).
Recreational activities including off
highway vehicles (OHV), all-terrain
vehicles (ATV), motorcycles, mountain
biking and other mechanized methods
of travel have been recognized as a
potential direct and indirect threat to
Gunnison sage-grouse and their habitat
(BLM 2009, p. 36). In Colorado, the
number of annual off highway vehicle
(OHV) registrations has increased from
12,000 in 1991 to 131,000 in 2007 (BLM
2009, p. 37). Four wheel drive, OHV,
motorcycle, specialty vehicle, and
mountain bike use is expected to
increase in the future based on
increased population in general and
increased population density in the area
(as discussed above). Numerous off-road
routes and access points to habitat used
by Gunnison sage-grouse combined with
increasing capabilities for mechanized
travel and increased human population
further contribute to habitat
fragmentation.
Roads in the Gunnison Basin
Population Area – On BLM lands in the
Gunnison Basin there are currently
2,050 km (1,274 mi) of roads within 6.4
km (4 mi) of Gunnison sage-grouse leks.
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Eighty-seven percent of all Gunnison
sage-grouse nests were located less than
6.4 km (4 mi) from the lek of capture
(Apa 2004, p. 21). However, the BLM
proposes to reduce road length to 1,157
km (719 mi) (BLM 2010, p. 147).
Currently, 1,349 km (838 mi) of roads
accessible to 2-wheel drive passenger
cars exist in occupied Gunnison sagegrouse habitat in the Gunnison Basin.
Four-wheel-drive vehicle roads, as well
as motorcycle, mountain bike, horse,
and hiking trails are heavily distributed
throughout the range of Gunnison sagegrouse (BLM 2009, pp. 27, 55, 86),
which further increases the overall
density of roads and their direct and
indirect effects on Gunnison sagegrouse. User-created roads and trails
have increased since 2004 (BLM 2009,
p. 33), although we do not know the
percentage increase.
Using a spatial dataset of roads in the
Gunnison Basin we performed GIS
analyses on the potential effects of roads
to Gunnison sage-grouse and their
habitat. To account for secondary effects
from invasive weed spread from roads
(see discussion below in Invasive
Plants), we applied a 0.7 km (0.4 mi)
buffer (Bradley and Mustard 2006, p.
1146) to all roads in the Gunnison
Basin. Results of these analyses indicate
that approximately 85 percent of
occupied habitat in the Gunnison Basin
has an increased likelihood of current or
future road-related invasive weed
invasion. When all roads in the
Gunnison basin are buffered by 6.4 km
(4 mi) or 9.6 km (6 mi) to account for
nesting avoidance (Aldridge et al. 2010,
p. 27) and secondary effects from
mammal and corvid foraging areas
(Knick et al in press, p. 113),
respectively, all occupied habitat in the
Gunnison Basin is indirectly affected by
roads.
Roads in All Other Population Areas
– Approximately 140 km (87 mi), 243
km (151 mi), and 217 km (135 mi) of
roads (all road classes) occur on BLM
lands within the Cerro Summit–
Cimarron–Sims Mesa, Crawford, and
San Miguel Basin population areas,
respectively, all of which are managed
by the BLM (BLM 2009, p. 71). We do
not have information on the total length
of roads within the Monticello–Dove
˜
Creek, Pınon Mesa, or Poncha Pass
Gunnison sage-grouse populations.
However, several maps provided by the
BLM show that roads are widespread
and common throughout these
population areas (BLM 2009, pp. 27, 55,
86).
Summary of Roads
As described above in the ‘Residential
Development’ section, the human
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population is increasing throughout the
range of Gunnison sage-grouse (CDOLA
2009a, pp. 2-3; CWCB 2009, p. 15), and
we have no data indicating this trend
will be reversed. Gunnison sage-grouse
are dependent on large contiguous and
unfragmented landscapes to meet their
life-history needs (GSRSC 2005, pp. 2630), and the existing road density
throughout much of the range of
Gunnison sage-grouse has negatively
affected the species. The collective
influences of fragmentation and
disturbance from roads reduce the
effective habitat around these areas
making them inhospitable to sagegrouse (Aldridge et al. 2010, pp. 24-25;
Aldridge and Boyce 2007, p. 520; Knick
et al. 2009, in press, p. 25 and references
therein). Given the current human
demographic and economic trends
described above in the Residential
Development section, we believe that
increased road use and increased road
construction associated with residential
development will continue at least
through 2050, and likely longer. The
resulting habitat loss, degradation, and
fragmentation from roads is a significant
threat to Gunnison sage-grouse now and
in the foreseeable future.
Powerlines
Powerlines can directly affect greater
sage-grouse by posing a collision and
electrocution hazard (Braun 1998, pp.
145-146; Connelly et al. 2000a, p. 974),
and can have indirect effects by
decreasing lek recruitment (Braun et al.
2002, p. 10), increasing predation
(Connelly et al. 2004, p. 13-12),
fragmenting habitat (Braun 1998, p.
146), and facilitating the invasion of
exotic annual plants (Knick et al. 2003,
p. 612; Connelly et al. 2004, p. 7-25).
Proximity to powerlines is associated
with Gunnison and greater sage-grouse
extirpation (Wisdom et al. in press, p.
20). Due to the potential spread of
invasive species and predators as a
result of powerline construction and
maintenance, the impact from a
powerline is greater than its actual
footprint. We believe the effects to
Gunnison sage-grouse are similar to
those observed in greater sage-grouse
and that the impact from a powerline is
greater than its footprint.
In areas where the vegetation is low
and the terrain relatively flat, power
poles provide an attractive hunting and
roosting perch, as well as nesting
stratum for many species of raptors and
corvids (Steenhof et al. 1993, p. 27;
Connelly et al. 2000a, p. 974; Manville
2002, p. 7; Vander Haegen et al. 2002,
p. 503). Power poles increase a raptor’s
range of vision, allow for greater speed
during attacks on prey, and serve as
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territorial markers (Steenhof et al. 1993,
p. 275; Manville 2002, p. 7). Raptors
may actively seek out power poles
where natural perches are limited. For
example, within 1 year of construction
of a 596-km (3–2 -mi) transmission line
in southern Idaho and Oregon, raptors
and common ravens began nesting on
the supporting poles (Steenhof et al.
1993, p. 275). Within 10 years of
construction, 133 pairs of raptors and
ravens were nesting along this stretch
(Steenhof et al. 1993, p. 275). Raven
counts increased by approximately 200
percent along the Falcon-Gondor
transmission line corridor in Nevada
within 5 years of construction (Atamian
et al. 2007, p. 2). The increased
abundance of raptors and corvids within
occupied greater and Gunnison sagegrouse habitats can result in increased
predation. Ellis (1985, p. 10) reported
that golden eagle (Aquila chryrsaetos)
predation on sage-grouse on leks
increased from 26 to 73 percent of the
total predation after completion of a
transmission line within 200 meters (m)
(220 yards (yd)) of an active sage-grouse
lek in northeastern Utah. The lek was
eventually abandoned, and Ellis (1985,
p. 10) concluded that the presence of
the powerline resulted in changes in
sage-grouse dispersal patterns and
caused fragmentation of the habitat.
Golden eagles are found throughout the
range of Gunnison sage-grouse (USGS
2010, p. 1), and golden eagles were
found to be the dominant species
recorded perching on power poles in
Utah in Gunnison sage-grouse habitat
(Prather and Messmer 2009, p. 12).
Leks within 0.4 km (0.25 mi) of new
powerlines constructed for coalbed
methane development in the Powder
River Basin of Wyoming had
significantly lower growth rates, as
measured by recruitment of new males
onto the lek, compared to leks further
from these lines, presumably resulting
from increased raptor predation (Braun
et al. 2002, p. 10). Within their analysis
area, Connelly et al. (2004, p. 7-26)
assumed a 5 to 6.9-km (3.1 to 4.3-mi)
radius buffer around the perches, based
on the average foraging distance of these
corvids and raptors, and estimated that
the area potentially influenced by
additional perches provided by
powerlines was 672,644 to 837,390 km2
(259,641 to 323,317 mi2), or 32 to 40
percent of their assessment area. The
actual impact on an area would depend
on corvid and raptor densities within
the area (see discussion in Factor C,
below).
The presence of a powerline may
fragment sage-grouse habitats even if
raptors are not present. The use of
otherwise suitable habitat by sage-
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grouse near powerlines increased as
distance from the powerline increased
for up to 600 m (660 yd) (Braun 1998,
p. 8). Based on those unpublished data,
Braun (1998, p. 8) reported that the
presence of powerlines may limit
Gunnison and greater sage-grouse use
within 1 km (0.6 mi) in otherwise
suitable habitat. Similar results were
recorded for other grouse species. For
example, lesser and greater prairiechickens (Tympanuchus pallidicinctus
and T. cupido, respectively) avoided
otherwise suitable habitat near
powerlines (Pruett et al. 2009, p. 6).
Additionally, both species also crossed
powerlines less often than nearby roads,
which suggests that powerlines are a
particularly strong barrier to movement
(Pruett et al. 2009, p. 6).
Sage-grouse also may avoid
powerlines as a result of the
electromagnetic fields present (Wisdom
et al. in press, p. 19). Electromagnetic
fields have been demonstrated to alter
the behavior, physiology, endocrine
systems and immune function in birds,
with negative consequences on
reproduction and development (Fernie
and Reynolds 2005, p. 135). Birds are
diverse in their sensitivities to
electromagnetic field exposures, with
domestic chickens being very sensitive.
Many raptor species are less affected
(Fernie and Reynolds 2005, p. 135). No
studies have been conducted
specifically on sage-grouse. Therefore,
we do not know the impact to the
Gunnison sage-grouse from
electromagnetic fields.
Linear corridors through sagebrush
habitats can facilitate the spread of
invasive species, such as cheatgrass
(Bromus tectorum) (Gelbard and Belnap
2003, pp. 424-426; Knick et al. 2003, p.
620; Connelly et al. 2004, p. 1-2).
However, we were unable to find any
information regarding the amount of
invasive species incursion as a result of
powerline construction.
Powerlines in the Gunnison Basin
Population Area – On approximately
121,000 ha (300,000 ac) of BLM land in
the Gunnison Basin, 36 rights-of-way for
power facilities, power lines, and
transmission lines have resulted in the
direct loss of 350 ha (858 ac) of
occupied habitat (Borthwick 2005b, pers
comm.). As discussed above, the
impacts of these lines likely extend
beyond their actual footprint. We
performed a GIS analysis of
transmission line location in relation to
overall habitat area and Gunnison sagegrouse lek locations in the Gunnison
Basin Population area to obtain an
estimate of the potential effects in the
Basin. Results of these analyses indicate
that 68 percent of the Gunnison Basin
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population area is within 6.9 km (4.3
mi) of an electrical transmission line
and is potentially influenced by avian
predators utilizing the additional
perches provided by transmission lines.
This area contains 65 of 109 active leks
(60 percent) in the Gunnison Basin
population. These results suggest that
potential increased predation resulting
from transmission lines have the
potential to affect a substantial portion
of the Gunnison Basin population.
Powerlines in All Other Population
Areas – A transmission line runs
through the Dry Creek Basin group in
the San Miguel Basin population, and
the Beaver Mesa group has two
transmission lines. None of the
transmission lines in the San Miguel
Basin have raptor proofing, nor do most
distribution lines (Ferguson 2005, pers
comm.) so their use by raptors and
corvids as perch sites for hunting and
use for nest sites is not discouraged.
One major electric transmission line
runs east-west in the northern portion of
the current range of the Monticello
group (San Juan County Gunnison Sagegrouse Working Group (GSWG) 2005, p.
17). Powerlines do not appear to be
present in sufficient density to pose a
significant threat to Gunnison sage˜
grouse in the Pınon Mesa population at
this time. One transmission line
parallels Highway 92 in the Crawford
population, and distribution lines run
from there to homes on the periphery of
the current range (Ferguson 2005, pers.
comm.).
Summary of Powerlines
The projected human population
growth rate in and near most Gunnison
sage-grouse populations is high (see
discussion under Residential
Development). As a result, we expect an
associated increase in distribution
powerlines. Powerlines are likely
negatively affecting Gunnison sagegrouse as they contribute to habitat loss
and fragmentation and facilitation of
predators of Gunnison sage-grouse.
Given the current demographic and
economic trends described above, we
believe that existing powerlines and
anticipated distribution of powerlines
associated with residential development
will continue at least through 2050, and
likely longer. The resulting habitat loss
and fragmentation from powerlines, and
the effects of avian predators that use
them, is a significant threat to Gunnison
sage-grouse now and in the foreseeable
future.
Fire
The nature of historical fire patterns
in sagebrush communities, particularly
in Wyoming big sagebrush (Artemisia
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tridentata var. wyomingensis), is not
well understood, and a high degree of
variability likely occurred (Miller and
Eddleman 2000, p. 16; Zouhar et al.
2008, p. 154; Baker in press, p. 16). In
general, mean fire return intervals in
low-lying, xeric (dry) big sagebrush
communities range from more than 100
to 350 years, and return intervals
decrease from 50 to more than 200 years
in more mesic (wet) areas, at higher
elevations, during wetter climatic
periods, and in locations associated
with grasslands (Baker 2006, p. 181;
Mensing et al. 2006, p. 75; Baker, in
press, pp. 15-16; Miller et al., in press,
p. 35).
Mountain big sagebrush (Artemisia
tridenata var. vaseyana), the most
important and widespread sagebrush
species for Gunnison sage-grouse, is
killed by fire and can require decades to
recover. In nesting and wintering sites,
fire causes direct loss of habitat due to
reduced cover and forage (Call and
Maser 1985, p. 17). While there may be
limited instances where burned habitat
is beneficial, these gains are lost if
alternative sagebrush habitat is not
readily available (Woodward 2006, p.
65).
Herbaceous understory vegetation
plays a critical role throughout the
breeding season as a source of forage
and cover for Gunnison sage-grouse
females and chicks. The response of
herbaceous understory vegetation to fire
varies with differences in species
composition, pre-burn site condition,
fire intensity, and pre- and post-fire
patterns of precipitation. In general,
when not considering the synergistic
effects of invasive species, any
beneficial short-term flush of understory
grasses and forbs is lost after only a few
years and little difference is apparent
between burned and unburned sites
(Cook et al. 1994, p. 298; Fischer et al.
1996, p. 196; Crawford 1999, p. 7;
Wrobleski 1999, p. 31; Nelle et al. 2000,
p. 588; Paysen et al. 2000, p. 154;
Wambolt et al. 2001, p. 250).
In addition to altering plant
community structure, fires can
influence invertebrate food sources
(Schroeder et al. 1999, p. 5). However,
because few studies have been
conducted and the results of those
available vary, the specific magnitude
and duration of the effects of fire on
insect communities is still uncertain.
A clear positive response of Gunnison
or greater sage-grouse to fire has not
been demonstrated (Braun 1998, p. 9).
The few studies that have suggested fire
may be beneficial for greater sage-grouse
were primarily conducted in mesic
areas used for brood-rearing (Klebenow
1970, p. 399; Pyle and Crawford 1996,
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p. 323; Gates 1983, in Connelly et al.
2000c, p. 90; Sime 1991, in Connelly et
al. 2000a, p. 972). In this type of habitat,
small fires may maintain a suitable
habitat mosaic by reducing shrub
encroachment and encouraging
understory growth. However, without
available nearby sagebrush cover, the
utility of these sites is questionable,
especially within the six small
Gunnison sage-grouse populations
where fire could further degrade and
fragment the remaining habitat.
Sagebrush loss as a result of fire is likely
to have proportionally more individual
bird and population level impacts as the
amount of sagebrush declines within
each of the remaining populations. As
the amount of sagebrush remaining
within a population declines, the greater
the potential impact is to that
population.
The invasion of the exotic cheatgrass
increases fire frequency within the
sagebrush ecosystem (Zouhar et al.
2008, p. 41; Miller et al. in press, p. 39).
Cheatgrass readily invades sagebrush
communities, especially disturbed sites,
and changes historical fire patterns by
providing an abundant and easily
ignitable fuel source that facilitates fire
spread. While sagebrush is killed by fire
and is slow to reestablish, cheatgrass
recovers within 1 to 2 years of a fire
event (Young and Evans 1978, p. 285).
This annual recovery leads to a readily
burnable fuel source and ultimately a
reoccurring fire cycle that prevents
sagebrush reestablishment (Eiswerth et
al. 2009, p. 1324). The extensive
distribution and highly invasive nature
of cheatgrass poses substantial increased
risk of fire and permanent loss of
sagebrush habitat, as areas disturbed by
fire are highly susceptible to further
invasion and ultimately habitat
conversion to an altered community
state. For example, Link et al. (2006, p.
116) show that risk of fire increases
from approximately 46 to 100 percent
when ground cover of cheatgrass
increases from 12 to 45 percent or more.
We do not have a reliable estimate of the
amount of area occupied by cheatgrass
in the range of Gunnison sage-grouse.
However, cheatgrass is found at
numerous locations throughout the
Gunnison Basin (BLM 2009, p. 60).
Fire in the Gunnison Basin Population
Area – Six prescribed burns have
occurred on BLM lands in the Gunnison
Basin since 1984, totaling
approximately 409 ha (1,010 ac) (BLM
2009, p. 35). The fires created large
sagebrush-free areas that were further
degraded by poor post-burn livestock
management (BLM 2005a, p. 13). As a
result, these areas are no longer suitable
as Gunnison sage-grouse habitat.
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Approximately 8,470 ha (20,930 ac) of
prescribed burns occurred on Forest
Service lands in the Gunnison Basin
since 1983 (USFS 2009, p. 1). A small
wildfire on BLM lands near Hartman
Rocks burned 8 ha (20 ac) in 2007 (BLM
2009, p. 35). The total area of occupied
Gunnison sage-grouse habitat burned in
recent decades is approximately 8,887
ha (21,960 ac), which constitutes 1.5
percent of the occupied Gunnison sagegrouse habitat area. Cumulatively, this
equates to a relatively small amount of
habitat burned over a period of nearly
three decades. This information suggests
that there has not been a demonstrated
change in fire cycle in the Gunnison
Basin population area to date.
Fire in All Other Population Areas –
Two prescribed burns conducted in
1986 (105 ha (260 ac)) and 1992 (140 ha
(350 ac)) on BLM land in the San Miguel
Basin on the north side of Dry Creek
Basin had negative impacts on sagegrouse. The burns were conducted for
big game forage improvement, but the
sagebrush died and was largely replaced
with weeds (BLM 2005b, pp. 7-8). The
Burn Canyon fire in the Dry Creek Basin
and Hamilton Mesa areas burned 890 ha
(2,200 ac) in 2000. Three fires have
occurred in Gunnison sage-grouse
habitat since 2004 on lands managed by
the BLM in the Crawford, Cerro
Summit–Cimarron–Sims Mesa, and San
Miguel Basin population areas. There
have been no fires since 2004 on lands
managed by the BLM within the
Monticello–Dove Creek population.
Because these fires were mostly small in
size, we do not believe they resulted in
substantial impacts to Gunnison sagegrouse.
Several wildfires near or within the
˜
Pınon Mesa population area have
occurred in the past 20 years. One fire
burned a small amount of occupied
Gunnison sage-grouse habitat in 1995,
and several fires burned in potential
Gunnison sage-grouse habitat.
Individual burned areas ranged from 3.6
ha (9 ac) to 2,160 ha (5,338 ac). A
wildfire in 2009 burned 1,053 ha (2,602
ac), predominantly within vacant or
unknown Gunnison sage-grouse habitat
(suitable habitat for sage-grouse that is
separated from occupied habitats that
has not been adequately inventoried, or
without recent documentation of grouse
˜
presence) near the Pınon Mesa
population. Since 2004, a single 2.8 ha
(7 ac) wildfire occurred in the Cerro
Summit–Cimarron–Sims Mesa
population area, and two prescribed
fires, both less than 12 ha (30 ac), were
implemented in the San Miguel
population area. There was no fire
activity within occupied Gunnison sagegrouse habitat in the last two decades in
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the Poncha Pass population area (CDOW
2009a, pp. 125-126) or the Monticello–
Dove Creek population area (CDOW
2009a, p. 75; UDWR 2009, p. 5).
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Summary of Fire
Fires can cause the proliferation of
weeds and can degrade suitable sagegrouse habitat, which may not recover
to suitable conditions for decades, if at
all (Pyke in press, pp. 18-19). Recent
fires in Gunnison sage-grouse habitat
were mostly small in size and did not
result in substantial impacts to
Gunnison sage-grouse, and there has
been no obvious change in fire cycle in
any Gunnison sage-grouse population
area. Therefore, we do not consider fire
to be a significant threat to Gunnison
sage-grouse or its habitat at this time. It
is not currently possible to predict the
extent or location of future fire events.
However, existing data indicates that
climate change has the potential to alter
changes in the distribution and extent of
cheatgrass and sagebrush and associated
fire frequencies. The best available data
indicates that fire frequency may
increase in the foreseeable future (which
we consider to be indefinite) because of
increases in cover of cheatgrass (Zouhar
et al. 2008, p. 41; Miller et al. in press,
p. 39; Whisenant 1990, p. 4) and the
projected effects of climate change
(Miller et al. in press, p. 47; Prevey et
al. 2009, p. 11) (see Invasive Plants and
Climate Change discussions below).
Therefore, fire is likely to become an
increasingly significant threat to the
Gunnison sage-grouse in the foreseeable
future.
Invasive Plants
For the purposes of this finding, we
define invasive plants as those that are
not native to an ecosystem and that have
a negative impact on Gunnison sagegrouse habitat. Invasive plants alter
native plant community structure and
composition, productivity, nutrient
cycling, and hydrology (Vitousek 1990,
p. 7) and may cause declines in native
plant populations through competitive
exclusion and niche displacement,
among other mechanisms (Mooney and
Cleland 2001, p. 5446). Invasive plants
reduce and, in cases where
monocultures of them occur, eliminate
vegetation that sage-grouse use for food
and cover. Invasive plants do not
provide quality sage-grouse habitat.
Sage-grouse depend on a variety of
native forbs and the insects associated
with them for chick survival, and
sagebrush, which is used exclusively
throughout the winter for food and
cover.
Along with replacing or removing
vegetation essential to sage-grouse,
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invasive plants fragment existing sagegrouse habitat. They can create longterm changes in ecosystem processes,
such as fire-cycles (see discussion under
Fire above) and other disturbance
regimes that persist even after an
invasive plant is removed (Zouhar et al.
2008, p. 33). A variety of nonnative
annuals and perennials are invasive to
sagebrush ecosystems (Connelly et al.
2004, pp. 7-107 and 7-108; Zouhar et al.
2008, p. 144). Cheatgrass is considered
most invasive in Artemisia tridentata
ssp. wyomingensis communities
(Connelly et al. 2004, p. 5-9). Other
invasive plants found within the range
of Gunnison sage-grouse that are
reported to take over large areas include:
spotted knapweed (Centaurea
maculosa), Russian knapweed
(Acroptilon repens), oxeye daisy
(Leucanthemum vulgare), yellow
toadflax (Linaria vulgaris), and field
bindweed (Convolvulus arvensis) (BLM
2009, p. 28, 36; Gunnison Watershed
Weed Commission (GWWC) 2009, pp. 46). Although not yet reported to create
large expanses in the range of Gunnison
sage-grouse, the following weeds are
also known from the species’ range and
do cover large expanses in other parts of
western North America: diffuse
knapweed (Centaurea diffusa), whitetop
(Cardaria draba), jointed goatgrass
(Aegilops cylindrica), and yellow
starthistle (Centaurea solstitialis). Other
invasive plant species present within
the range of Gunnison sage-grouse that
are problematic yet less likely to
overtake large areas include: Canada
thistle (Cirsium arvense), musk thistle
(Carduus nutans), bull thistle (Cirsium
vulgare), houndstongue (Cynoglossum
officinale), black henbane (Hyoscyamus
niger), common tansy (Tanacetum
vulgare), and absinth wormwood
(Artemisia biennis) (BLM 2009, p. 28,
36; GWWC 2009, pp. 4-6).
Cheatgrass impacts sagebrush
ecosystems by potentially shortening
fire intervals from several decades,
depending on the type of sagebrush
plant community and site productivity,
to as low as 3 to 5 years, perpetuating
its own persistence and intensifying the
role of fire (Whisenant 1990, p. 4).
Connelly et al. (2004, p. 7-5) suggested
that cheatgrass shortens fire intervals to
less than 10 years. As discussed under
the discussion of climate change below,
temperature increases may increase the
competitive advantage of cheatgrass in
higher elevation areas where its current
distribution is limited (Miller et al. in
press, p. 47). Decreased summer
precipitation reduces the competitive
advantage of summer perennial grasses,
reduces sagebrush cover, and
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59821
subsequently increases the likelihood of
cheatgrass invasion (Bradley 2009, pp.
202-204; Prevey et al. 2009, p. 11). This
could increase the susceptibility of
sagebrush areas in Utah and Colorado to
cheatgrass invasion (Bradley 2009, p.
204).
A variety of restoration and
rehabilitation techniques are used to
treat invasive plants, but they can be
costly and are mostly unproven and
experimental at a large scale. In the last
approximately 100 years, no broad-scale
cheatgrass eradication method has been
developed. Habitat treatments that
either disturb the soil surface or deposit
a layer of litter increase cheatgrass
establishment in the Gunnison Basin
when a cheatgrass seed source is present
(Sokolow 2005, p. 51). Therefore,
researchers recommend using habitat
treatment tools, such as brush mowers,
with caution and suggest that treated
sites should be monitored for increases
in cheatgrass emergence (Sokolow 2005,
p. 49).
Invasive Plants in the Gunnison Basin
Population Area – Quantifying the total
amount of Gunnison sage-grouse habitat
impacted by invasive plants is difficult
due to differing sampling
methodologies, incomplete sampling,
inconsistencies in species sampled, and
varying interpretations of what
constitutes an infestation (Miller et al.,
in press, p. 19). Cheatgrass has invaded
areas in Gunnison sage-grouse range,
supplanting sagebrush habitat in some
areas. However, we do not have a
reliable estimate of the amount of area
occupied by cheatgrass in the range of
Gunnison sage-grouse. While not
ubiquitous, cheatgrass is found at
numerous locations throughout the
Gunnison Basin (BLM 2009, p. 60).
Cheatgrass infestation within a
particular area can range from a small
number of individuals scattered
sparsely throughout a site, to complete
or near-complete understory domination
of a site. Cheatgrass has increased
throughout the Gunnison Basin in the
last decade and is becoming
increasingly detrimental to sagebrush
community types (BLM 2009, p. 7).
Currently in the Gunnison Basin,
cheatgrass attains site dominance most
often along roadways; however, other
highly disturbed areas have similar
cheatgrass densities. Cheatgrass is
currently present in almost every
grazing allotment in Gunnison sagegrouse occupied habitat and other
invasive plant species, such as Canada
thistle, black henbane, spotted
knapweed, Russian knapweed, Kochia,
bull thistle, musk thistle, oxeye daisy,
yellow toadflax and field bindweed, are
found in riparian areas and roadsides
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throughout the Gunnison Basin (BLM
2009, p. 7).
Although disturbed areas most often
contain the highest cheatgrass densities,
cheatgrass can readily spread into less
disturbed and even undisturbed habitat.
A strong indicator for future cheatgrass
locations is the proximity to current
locations (Bradley and Mustard 2006, p.
1146) as well as summer, annual, and
spring precipitation, and winter
temperature (Bradley 2009, p. 196).
Although we lack the information to
make a detailed determination on the
actual extent or rate of increase, given
its invasive nature, we believe
cheatgrass and its negative influence on
Gunnison sage-grouse will increase in
the Gunnison Basin in the future
because of potential exacerbation from
climate change interactions and the
limited success of broad-scale control
efforts.
Invasive Plants in All Other
Population Areas – Cheatgrass is
present throughout much of the current
range in the San Miguel Basin (BLM
2005c, p. 62005d), but is most abundant
in the Dry Creek Basin group (CDOW
2005a, p. 101), which comprises 62
percent of the San Miguel Basin
population. It is present in the five
Gunnison sage-grouse subpopulations
east of Dry Creek Basin although at
much lower densities and does not
currently pose a serious threat to
Gunnison sage-grouse (CDOW 2005a, p.
101). Invasive species are present at low
levels in the Monticello group (San Juan
County GSGWG 2005, p. 20). However,
there is no evidence that they are
affecting the population. Cheatgrass
dominates 10–15 percent of the
sagebrush understory in the current
˜
range of the Pınon Mesa population
(Lambeth 2005, pers comm.). It occurs
in the lower elevation areas below
˜
Pınon Mesa that were formerly
Gunnison sage-grouse range. Cheatgrass
invaded two small prescribed burns in
or near occupied habitat conducted in
1989 and 1998 (BLM 2005d, p. 62005a),
and continues to be a concern with new
ground-disturbing projects. Invasive
plants, especially cheatgrass, occur
primarily along roads, other disturbed
areas, and isolated areas of untreated
vegetation in the Crawford population.
The threat of cheatgrass may be greater
to sage-grouse than all other nonnative
species combined and could be a
significant limiting factor when and if
disturbance is used to improve habitat
conditions, unless mitigated (BLM
2005c, p. 6). No current estimates of the
extent of weed invasion are available
(BLM 2005c, p. 82005d).
˜
Within the Pınon Mesa Gunnison
sage-grouse population area, 520 ha
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(1,284 ac) of BLM lands are currently
mapped with cheatgrass as the
dominant species (BLM 2009, p. 3). This
is not a comprehensive inventory of
cheatgrass occurrence, as it only
includes areas where cheatgrass
dominates the plant community and
does not include areas where the
species is present at lower densities.
Cheatgrass distribution has not been
comprehensively mapped for the
Monticello–Dove Creek population area;
however, cheatgrass is beginning to be
assessed on a site-specific and projectlevel basis. No significant invasive plant
occurrences are currently known in the
Poncha Pass population area.
Summary of Invasive Plants
Invasive plants negatively impact
Gunnison sage-grouse primarily by
reducing or eliminating native
vegetation that sage-grouse require for
food and cover, resulting in habitat loss
and fragmentation. Although invasive
plants, especially cheatgrass, have
affected some Gunnison sage-grouse
habitat, the impacts do not currently
appear to be threatening individual
populations or the species rangewide.
However, invasive plants continue to
expand their range, facilitated by
ground disturbances such as fire,
grazing, and human infrastructure.
Climate change will likely alter the
range of individual invasive species,
increasing fragmentation and habitat
loss of sagebrush communities. Even
with treatments, given the history of
invasive plants on the landscape, and
our continued inability to control such
species, we anticipate invasive plants
will persist and will likely continue to
spread throughout the range of the
species. Therefore, invasive plants and
associated fire risk will be on the
landscape for the foreseeable future.
Although currently not a significant
threat to the Gunnison sage-grouse at
the species level, we anticipate invasive
species to become an increasingly
significant threat to the species in the
foreseeable future, particularly when
considered in conjunction with future
climate projections and potential
changes in sagebrush plant community
composition and dynamics.
˜
Pınon-Juniper Encroachment
˜
Pınon-juniper woodlands are a native
˜
habitat type dominated by Pınon pine
(Pinus edulis) and various juniper
species (Juniperus spp.) that can
encroach upon, infill, and eventually
˜
replace sagebrush habitat. Pınon-juniper
extent has increased 10-fold in the
Intermountain West since
EuroAmerican settlement, causing the
loss of many bunchgrass and sagebrush-
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bunchgrass communities (Miller and
˜
Tausch 2001, pp. 15-16). Pınon-juniper
woodlands have also been expanding
throughout portions of the range of
Gunnison sage-grouse (BLM 2009, pp.
˜
14, 17, 25). Pınon-juniper expansion has
been attributed to the reduced role of
fire, the introduction of livestock
grazing, increases in global carbon
dioxide concentrations, climate change,
and natural recovery from past
disturbance (Miller and Rose 1999, pp.
555-556; Miller and Tausch 2001, p. 15;
Baker, in press, p. 24). In addititon,
Gambel oak invasion as a result of fire
suppression also has been identified as
a potential threat to Gunnison sagegrouse (CDOW 2002, p. 139).
Similar to powerlines, trees provide
perches for raptors, and as a
consequence, Gunnison sage-grouse
˜
avoid areas with Pınon-juniper
(Commons et al. 1999, p. 239). The
number of male Gunnison sage-grouse
on leks in southwest Colorado doubled
˜
after Pınon-juniper removal and
mechanical treatment of mountain
sagebrush and deciduous brush
(Commons et al. 1999, p. 238).
˜
Pınon-Juniper Encroachment in All
Population Areas – We have no
information indicating that the
Gunnison Basin population area is
˜
currently undergoing significant Pınonjuniper encroachment. A significant
˜
portion of the Pınon Mesa population is
˜
undergoing Pınon-juniper
encroachment. Approximately 9 percent
(1,140 ha [3,484 ac]) of occupied habitat
˜
in the Pınon Mesa population area have
˜
Pınon-juniper coverage, while 7 percent
(4,414 ha [10,907 ac)] of vacant or
unknown and 13 percent (7,239 ha
[17,888 ac]) of potential habitat
(unoccupied habitats that could be
suitable for occupation of sage-grouse if
practical restoration were applied) have
encroachment (BLM 2009, p. 17).
Some areas on lands managed by the
˜
BLM are known to be undergoing Pınonjuniper invasion. However, the extent of
the area affected has not been quantified
(BLM 2009, p. 74; BLM 2009, p. 9).
Approximately 9 percent of the 1,300 ha
(3,200 ac) of the current range in the
Crawford population is classified as
˜
dominated by Pınon-juniper (GSRSC
2005, p. 264). However, BLM (2005d, p.
8) estimates that as much as 20 percent
of the population area is occupied by
˜
˜
Pınon-juniper. Pınon and juniper trees
have been encroaching in peripheral
habitat on Sims Mesa, and to a lesser
extent on Cerro Summit, but not to the
point where it is a serious threat to the
Cerro Summit–Cimarron–Sims Mesa
population area (CDOW 2009a, p. 47).
˜
Pınon and juniper trees are reported to
be encroaching throughout the current
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range in the Monticello group, based on
a comparison of historical versus
current aerial photos, but no
quantification or mapping of the
encroachment has occurred (San Juan
County GSWG 2005, p. 20). A relatively
˜
recent invasion of Pınon and juniper
trees between the Dove Creek and
Monticello groups appears to be
contributing to their isolation from each
other (GSRSC 2005, p. 276).
Within the range of Gunnison sagegrouse, approximately 5,341 ha (13,197
˜
ac) of Pınon-juniper have been treated
with various methods designed to
˜
remove Pınon and juniper trees since
2005, and nearly half of which occurred
˜
in the Pınon Mesa population (CDOW
2009c, entire). Mechanical treatment of
˜
areas experiencing Pınon-juniper
encroachment continues to be one of the
most successful and economical habitat
treatments for the benefit of Gunnison
sage-grouse.
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˜
Summary of Pınon-Juniper
Encroachment
Most Gunnison sage-grouse
population areas are experiencing low
˜
to moderate levels of Pınon-juniper
˜
encroachment; however, Pınon-juniper
˜
encroachment in the Pınon Mesa
population has been significant. The
˜
encroachment of Pınon-juniper into
sagebrush habitats contributes to the
fragmentation of Gunnison sage-grouse
˜
habitat. However, Pınon-juniper
treatments, particularly when
completed in the early stages of
encroachment when the sagebrush and
forb understory is still intact, have the
potential to provide an immediate
benefit to sage-grouse. Approximately
˜
5,341 ha (13,197 ac) of Pınon-juniper
encroachment within the range of
Gunnison sage-grouse has been treated.
˜
We expect Pınon-juniper encroachment
and corresponding treatment efforts to
continue into the foreseeable future,
which we consider to be indefinite for
˜
this threat. Although Pınon-juniper
encroachment is contributing to habitat
fragmentation in a limited area, the level
of encroachment is not sufficient to pose
a significant threat to Gunnison sagegrouse at a population or rangewide
level either now or in the foreseeable
˜
future. Pınon-juniper encroachment
may become an increasingly significant
threat to the Gunnison sage-grouse if
mechanical treatment of areas
˜
experiencing Pınon-juniper
encroachment declines, and if suitable
habitat continues to be lost due to other
threats such as residential and
associated infrastructure development.
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Domestic Grazing and Wild Ungulate
Herbivory
At least 87 percent of occupied
Gunnison sage-grouse habitat on Federal
lands is currently grazed by domestic
livestock (USFWS 2010c, entire). We
lack information on the proportion of
Gunnison sage-grouse habitat on private
lands that is currently grazed. Excessive
grazing by domestic livestock during the
late 1800s and early 1900s, along with
severe drought, significantly impacted
sagebrush ecosystems (Knick et al. 2003,
p. 616). Although current livestock
stocking rates in the range of Gunnison
sage-grouse are substantially lower than
historical levels (Laycock et al. 1996, p.
3), long-term effects from this
overgrazing, including changes in plant
communities and soils, persist today
(Knick et al. 2003, p.116).
Although livestock grazing and
associated land treatments have likely
altered plant composition, increased
topsoil loss, and increased spread of
exotic plants, the impacts on Gunnison
sage-grouse are not clear. Few studies
have directly addressed the effect of
livestock grazing on sage-grouse (Beck
and Mitchell 2000, pp. 998-1000;
Wamboldt et al. 2002, p. 7; Crawford et
al. 2004, p. 11), and little direct
experimental evidence links grazing
practices to Gunnison sage-grouse
population levels (Braun 1987, pp. 136137, Connelly and Braun 1997, p. 7-9).
Rowland (2004, p. 17-18) conducted a
literature review and found no
experimental research that demonstrates
grazing alone is responsible for
reduction in sage-grouse numbers.
Despite the obvious impacts of
grazing on plant communities within
the range of the species, the GSRSC
(2005, p. 114) could not find a direct
correlation between historic grazing and
reduced Gunnison sage-grouse numbers.
While implications on population-level
impacts from grazing can be made based
on impacts of grazing on individuals, no
studies have documented (positively or
negatively) the actual impacts of grazing
at the population level.
Sage-grouse need significant grass and
shrub cover for protection from
predators, particularly during nesting
season, and females will preferentially
choose nesting sites based on these
qualities (Hagen et al. 2007, p. 46). In
particular, nest success in Gunnison
sage-grouse habitat is related to greater
grass and forb heights and shrub density
(Young 1994, p. 38). The reduction of
grass heights due to livestock grazing in
sage-grouse nesting and brood-rearing
areas has been shown to negatively
affect nesting success when cover is
reduced below the 18 cm (7 in.) needed
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59823
for predator avoidance (Gregg et al.
1994, p. 165). Based on measurements
of cattle foraging rates on bunchgrasses
both between and under sagebrush
canopies, the probability of foraging on
under-canopy bunchgrasses depends on
sagebrush size and shape and,
consequently, the effects of grazing on
nesting habitats might be site specific
(France et al. 2008, pp. 392-393).
Several authors have noted that
grazing by livestock could reduce the
suitability of breeding and brood-rearing
habitat, negatively affecting sage-grouse
populations (Braun 1987, p. 137; Dobkin
1995, p. 18; Connelly and Braun 1997,
p. 231; Beck and Mitchell 2000, pp. 9981000). Domestic livestock grazing
reduces water infiltration rates and the
cover of herbaceous plants and litter,
compacts the soil, and increases soil
erosion (Braun 1998, p. 147; Dobkin et
al. 1998, p. 213). These impacts change
the proportion of shrub, grass, and forb
components in the affected area, and
facilitate invasion of exotic plant
species that do not provide suitable
habitat for sage-grouse (Mack and
Thompson 1982, p. 761; Miller and
Eddleman 2000, p. 19; Knick et al., in
press, p. 41).
Livestock may compete directly with
sage-grouse for rangeland resources.
Cattle are grazers, feeding mostly on
grasses, but they will make seasonal use
of forbs and shrub species like
sagebrush (Vallentine 1990, p. 226), a
primary source of nutrition for sagegrouse. A sage-grouse hen’s nutritional
condition affects nest initiation rate,
clutch size, and subsequent
reproductive success (Barnett and
Crawford 1994, p. 117; Coggins 1998, p.
30). Other effects of direct competition
between livestock and sage-grouse
depend on condition of the habitat and
the grazing practices. Thus, the effects
vary across the range of Gunnison sagegrouse. For example, poor livestock
management in mesic sites results in a
reduction of forbs and grasses available
to sage-grouse chicks, thereby affecting
chick survival (Aldridge and Brigham
2003, p. 30). Chick survival is one of the
most important factors in maintaining
Gunnison sage-grouse population
viability (GSRSC 2005, p. 173).
Livestock can trample sage-grouse and
its habitat. Although the effect of
trampling at a population level is
unknown, outright nest destruction has
been documented, and the presence of
livestock can cause sage-grouse to
abandon their nests (Rasmussen and
Griner 1938, p. 863; Patterson 1952, p.
111; Call and Maser 1985, p. 17;
Holloran and Anderson 2003, p. 309;
Coates 2007, p. 28). Coates (2007, p. 28)
documented nest abandonment
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following partial nest depredation by a
cow. In general, all recorded encounters
between livestock and grouse nests
resulted in hens flushing from nests,
which could expose the eggs to
predation. Visual predators like ravens
likely use hen movements to locate
sage-grouse nests (Coates 2007, p. 33).
Livestock also may trample sagebrush
seedlings, thereby removing a source of
future sage-grouse food and cover
(Connelly et al. 2004, pp. 7-31).
Trampling of soil by livestock can
reduce or eliminate biological soil crusts
making these areas susceptible to
cheatgrass invasion (Mack 1981, pp.
148-149; Young and Allen 1997, p. 531).
Livestock grazing may have positive
effects on sage-grouse under some
habitat conditions. Evans (1986, p. 67)
found that sage-grouse used grazed
meadows significantly more during late
summer than ungrazed meadows
because grazing had stimulated the
regrowth of forbs. Greater sage-grouse
sought out and used openings in
meadows created by cattle grazing in
northern Nevada (Klebenow 1981, p.
121). Also, both sheep and goats have
been used to control invasive weeds
(Mosley 1996 in Connelly et al. 2004,
pp. 7-49; Merritt et al. 2001, p. 4; Olsen
and Wallander 2001, p. 30) and woody
plant encroachment (Riggs and Urness
1989, p. 358) in sage-grouse habitat.
Sagebrush plant communities are not
adapted to domestic grazing
disturbance. Grazing changed the
functioning of systems into less
resilient, and in some cases, altered
communities (Knick et al., in press, p.
39). The ability to restore or rehabilitate
areas depends on the condition of the
area relative to the ability of a site to
support a specific plant community
(Knick et al., in press, p. 39). For
example, if an area has a balanced mix
of shrubs and native understory
vegetation, a change in grazing
management can restore the habitat to
its potential historic species
composition (Pyke, in press, p. 11).
Wambolt and Payne (1986, p. 318)
found that rest from grazing had a better
perennial grass response than other
treatments. Active restoration would be
required where native understory
vegetation is much reduced (Pyke, in
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press, p. 15). But, if an area has soil loss
or invasive species, returning the site to
the native historical plant community
may be impossible (Daubenmire 1970,
p. 82; Knick et al., in press, p. 39; Pyke,
in press, p. 17). Aldridge et al. (2008, p.
990) did not find any relationship
between sage-grouse persistence and
livestock densities. However, the
authors noted that livestock numbers do
not necessarily correlate with range
condition. They concluded that the
intensity, duration, and distribution of
livestock grazing are more influential on
rangeland condition than the livestock
density values used in their modeling
efforts (Aldridge et al. 2008, p. 990).
Currently, there is little direct evidence
linking grazing practices to population
levels of Gunnison or greater sagegrouse. Although grazing has not been
examined at large spatial scales, as
discussed above, we do know that
grazing can have negative impacts to
individuals, nests, breeding
productivity, and sagebrush and,
consequently, to sage-grouse at local
scales.
Public Lands Grazing in the Gunnison
Basin Population Area – Our analysis of
grazing is focused on BLM lands
because nearly all of the information
available to us regarding current grazing
management within the range of
Gunnison sage-grouse was provided by
the BLM. However, this information is
pertinent to over 40 percent of the land
area currently occupied by Gunnison
sage-grouse. A summary of domestic
livestock grazing management on BLM
and USFS lands in occupied Gunnison
sage-grouse habitat is provided in Table
3. The BLM manages approximately
122,376 ha (301,267 ac), or 51 percent
of the area currently occupied by
Gunnison sage-grouse in the Gunnison
Basin, and approximately 98 percent of
this area is actively grazed. The USFS
manages approximately 34,544 ha
(85,361 ac) or 14 percent of the
occupied portion of the Gunnison Basin
population area. In 2009, within the
occupied range in the Gunnison Basin
population, 13 of 62 (21 percent) active
BLM grazing allotments and 3 of 35 (9
percent) of USFS grazing allotments had
Gunnison sage-grouse habitat objectives
incorporated into the allotment
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management plans or Records of
Decision for permit renewals (USFWS
2010c, pp. 1-2). Habitat objectives for
Gunnison sage-grouse within allotment
management plans were designed such
that they provide good habitat for the
species when allotments are managed in
accordance with the objectives. In 2009,
57 percent of the area of occupied
habitat in active BLM grazing allotments
(45 percent of the entire Gunnison Basin
population area) had a recently
completed land health assessment
(LHA), and 94 percent of the area in
occupied habitat in active allotments
was deemed by the BLM as not meeting
LHA objectives specific to Gunnison
sage-grouse. The remainder of the LHAmonitored allotments were deemed to
be meeting objectives or as ‘‘unknown’’.
LHAs are assessments of the on-theground condition and represent the best
available information on the status of
the habitat. We are uncertain of habitat
conditions on the remaining 55 percent
of BLM lands in the Gunnison Basin.
Based on the assumption that the same
proportion of these lands are also not
meeting LHA objectives results in an
estimate of 94 percent of BLM lands in
the Gunnison Basin not meeting LHA
objectives specific to Gunnison sagegrouse habitat. This analysis indicates
that, without taking into account habitat
conditions on private lands and other
Federal and State lands, up to 48
percent of the entire Gunnison Basin
population area is not providing optimal
habitat conditions for Gunnison sagegrouse.
The fact that most grazing allotments
are not meeting LHA objectives
indicates that grazing is a factor that is
likely contributing to Gunnison sagegrouse habitat degradation. In addition,
grazing has negatively impacted several
Gunnison sage grouse treatments
(projects aimed at improving habitat
condition) in the Gunnison Basin (BLM
2009, p. 34). Although these areas are
generally rested for 2 years after
treatment, several have been heavily
used by cattle shortly after the
treatment, and the effectiveness of the
treatments decreased (BLM 2009, p. 34)
and reduced the potential benefits of the
treatments.
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TABLE 3. SUMMARY OF DOMESTIC LIVESTOCK GRAZING MANAGEMENT ON BLM AND USFS LANDS IN OCCUPIED HABITAT
FOR EACH OF THE GUNNISON SAGE-GROUSE POPULATIONS (FROM USFWSA 2010C, COMPILATION OF DATA PROVIDED
BY BLMB AND USFSC).
Percent
Number of Active USFS Allotments
Number of Active BLM Allotments
Active Allotments
with GUSGd
Objectives
BLM Allotments
with Completed
LHAe
Assessed BLM
Allotments
Meeting LHA
Objectives
34
62
21
66
22
no data
13
0
77
40
Dove Creek
n/a
3
0
0
0
Monticello
n/af
6
100
83
80
no data
15
53
27
100
Cerro Summit–Cimarron–Sims Mesa
n/af
10
10
50
40
Crawfordg
n/af
7
71
100
86
no data
8
13
100
100
34
63
59
Population
Gunnison
San Miguel Basin
Monticello–Dove Creek:
˜
Pinon Mesa
Poncha Pass
Rangewide Averages
aUnited
States Fish and Wildlife Service
of Land Management
States Forest Service
dGunnison sage-grouse
eLand Health Assessments
fNo United States Forest Service Land in occupied habitat in this population area.
fIncludes allotments on National Park Service lands but managed by the Bureau of Land Management.
bBureau
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cUnited
Public Lands Grazing in All Other
Population Areas – The BLM manages
approximately 36 percent of the area
currently occupied by Gunnison sagegrouse in the San Miguel Basin, and
approximately 79 percent of this area is
actively grazed. Within the occupied
range in the San Miguel population, no
active BLM grazing allotments have
Gunnison sage-grouse habitat objectives
incorporated into the allotment
management plans or Records of
Decision for permit renewals (USFWS
2010c, p. 9). In 2009, 10 of 15 (77
percent) active allotments had LHAs
completed in the last 15 years; 4 of 10
allotments (40 percent) were deemed by
the BLM to meet LHA objectives.
Gunnison sage-grouse habitat within the
60 percent of allotments not meeting
LHA objectives and the 5 allotments
with no LHAs completed are likely
being adversely impacted by grazing.
Therefore, it appears that grazing in a
large portion of this population area is
a factor that is likely contributing to
Gunnison sage-grouse habitat
degradation.
The BLM manages 11 percent of the
occupied habitat in the Dove Creek
group, and 41 percent of this area is
actively grazed. Within the occupied
range in the Dove Creek group of the
Monticello–Dove Creek population, no
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active BLM grazing allotments have
Gunnison sage-grouse habitat objectives
incorporated into the allotment
management plans or Records of
Decision for permit renewals (USFWS
2010c, p. 3). In 2009, no active
allotments in occupied habitat had
completed LHAs. Gunnison sage-grouse
are not explicitly considered in grazing
management planning, and the lack of
habitat data limits our ability to
determine the impact to the habitat on
public lands.
The BLM manages on 4 percent of the
occupied habitat in the Monticello
group, and 83 percent of this area is
grazed. Within the occupied range in
the Monticello group, 6 of 6 active BLM
grazing allotments have Gunnison sagegrouse habitat objectives incorporated
into the allotment management plans or
Records of Decision for permit renewals
(USFWS 2010c, p. 6). In 2009, 88
percent of the area of occupied habitat
in active allotments had a recently
completed LHA. Approximately 60
percent of the area in occupied habitat
in active allotments were deemed by the
BLM to meet LHA objectives. This
information suggests that grazing the
majority of lands managed by the BLM
is not likely significantly contributing to
Gunnison sage-grouse habitat
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degradation in the Monticello
population group.
The BLM manages 28 percent of
˜
occupied habitat in the Pınon Mesa
population area, and approximately 97
percent of this area is grazed. Over 50
percent of occupied habitat in this
population area is privately owned and,
while grazing certainly occurs on these
lands, we have no information on its
extent. Within the occupied range in the
˜
Pınon Mesa population, 8 of 15 (53
percent) active BLM grazing allotments
have Gunnison sage-grouse habitat
objectives incorporated into the
allotment management plans or Records
of Decision for permit renewals (USFWS
2010c, p. 5). In 2009, 23 percent of the
area of occupied Gunnison sage-grouse
˜
habitat in active allotments in the Pınon
Mesa population area had LHAs
completed in the last 15 years, and all
of these were deemed by the BLM to
meet LHA objectives. Therefore, for the
˜
portion of the Pınon Mesa population
area for which we have information, it
appears that grazing is not likely
significantly contributing to Gunnison
sage-grouse habitat degradation.
The BLM manages on 13 percent of
the occupied habitat in the Cerro
Summit–Cimarron–Sims Mesa
population area, and 83 percent of this
area is grazed. Within the occupied
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range in the Cerro Summit–Cimarron–
Sims Mesa population, 1 of 10 (10
percent) active BLM grazing allotments
have Gunnison sage-grouse habitat
objectives incorporated into the
allotment management plans or Records
of Decision for permit renewals (USFWS
2010c, p. 7). In 2009, 5 of the 10 active
allotments had LHAs completed in the
last 15 years and 3 (60 percent) of these
were deemed by the BLM as not meeting
LHA objectives. Therefore, for the small
portion of the Cerro Summit–Cimarron–
Sims Mesa population area for which
we have information, it appears that
grazing is a factor that is likely
contributing to some Gunnison sagegrouse habitat degradation.
Lands administered by the BLM and
NPS comprise over 75 percent of
occupied habitat in the Crawford
population, and 96 percent of this area
is actively grazed. Grazing allotments on
NPS lands in this area are administered
by the BLM. Within occupied range in
the Crawford population, 1 of 7 (14
percent) active BLM grazing allotments
have Gunnison sage-grouse habitat
objectives incorporated into the
allotment management plans or Records
of Decision for permit renewals (USFWS
2010c, p. 8). In 2009, all of the active
allotments had LHAs completed in the
last 15 years, and 86 percent were
deemed by the BLM to meet LHA
objectives. Seasonal forage utilization
levels were below 30 percent in most
Crawford Area allotments, although a
small number of allotments had nearly
50 percent utilization (BLM 2009x, p.
68). Based on this information, it
appears that grazing is not likely
significantly contributing to Gunnison
sage-grouse habitat degradation in the
majority of the Crawford population
area.
The BLM manages nearly half of
occupied habitat in the Poncha Pass
population area, and approximately 98
percent of this area is actively grazed.
Within the occupied range in the
Poncha Pass population, 1 of 8 (13
percent) active BLM grazing allotments
have Gunnison sage-grouse habitat
objectives incorporated into the
allotment management plans or Records
of Decision for permit renewals (USFWS
2010c, p. 4). In 2009, all active
allotments in occupied habitat had
completed LHAs, and all were meeting
LHA objectives. Based on this
information it appears that grazing is
not likely significantly contributing to
Gunnison sage-grouse habitat
degradation in the majority of the
Poncha Pass population area.
Non-federal Lands Grazing in All
Population Areas –Livestock grazing on
private and other non-federal lands,
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where present, has the potential to
impact Gunnison sage-grouse, but we
lack sufficient information to make an
assessment. Table 1 summarizes the
percentage of land area potentially
available to grazing within each of the
populations.
As discussed earlier, some private
lands are enrolled in the CRP program
and provide some benefits to Gunnison
sage-grouse. The CRP land in the
Monticello group has provided a
considerable amount of brood-rearing
habitat because of its forb component.
Grazing of CRP land in Utah occurred in
2002 under emergency Farm Bill
provisions due to drought and removed
at least some of the grass and forb
habitat component thus likely
negatively affecting Gunnison sagegrouse chick survival. Radio-collared
males and non-brood-rearing females
exhibited temporary avoidance of
grazed fields during and after grazing
(Lupis et al. 2006, pp. 959-960),
although one hen with a brood
continued to use a grazed CRP field.
This indicates that when CRP lands are
grazed, negative impacts to their habitat
and behavior may result. Since we have
very little information on the status of
Gunnison sage-grouse habitat on nonfederal lands, we cannot assess whether
the impacts that are occurring rise to the
level of being a threat.
Wild Ungulate Herbivory in All
Population Areas – Overgrazing by deer
and elk may cause local degradation of
habitats by removal of forage and
residual hiding and nesting cover.
Hobbs et al. (1996, pp. 210-213)
documented a decline in available
perennial grasses as elk densities
increased. Such grazing could
negatively impact nesting cover for sagegrouse. The winter range of deer and elk
overlaps the year-round range of the
Gunnison sage-grouse. Excessive but
localized deer and elk grazing has been
documented in the Gunnison Basin
(BLM 2005a, pp. 17-18; Jones 2005,
pers. comm.).
Grazing by deer and elk occurs in all
Gunnison sage-grouse population areas.
Although we have no information
indicating that competition for
resources is limiting Gunnison sagegrouse in the Gunnison Basin, BLM
observed that certain mountain shrubs
were being browsed heavily by wild
ungulates (BLM 2009, p. 34).
Subsequent results of monitoring in
mountain shrub communities indicated
that drought and big game were having
large impacts on the survivability and
size of mountain mahogany
(Cercocarpus utahensis), bitterbrush
(Purshia tridentata), and serviceberry
(Amelanchier alnifolia) in the Gunnison
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Basin (Jupuntich et al. 2010, pp. 7-9).
The authors raised concerns that
observed reductions in shrub size and
vigor will reduce drifting snow
accumulation, resulting in decreased
moisture availability to grasses and
forbs during the spring melt. Reduced
grass and forb growth could negatively
impact Gunnison sage-grouse nesting
and early brood-rearing habitat.
Grazing Summary
Livestock management and domestic
grazing have the potential to seriously
degrade Gunnison sage-grouse habitat.
Grazing can adversely impact nesting
and brood-rearing habitat by decreasing
vegetation available for concealment
from predators. Grazing also has been
shown to compact soils, decrease
herbaceous abundance, increase
erosion, and increase the probability of
invasion of exotic plant species.
The impacts of livestock operations
on Gunnison sage-grouse depend upon
stocking levels and season of use. We
recognize that not all livestock grazing
result in habitat degradation and many
livestock operations within the range of
Gunnison sage-grouse are employing
innovative grazing strategies and
conservation actions (Gunnison County
Stockgrowers 2009, entire). However,
available information suggests that LHA
objectives specific to Gunnison sagegrouse are not being met on more than
50 percent of BLM-managed occupied
Gunnison sage-grouse habitat in the
Gunnison Basin, San Miguel Basin, and
the Cerro Summit–Cimarron–Sims Mesa
population areas. Cumulatively, the
BLM-managed portion of these
populations constitutes approximately
33 percent of the entire range of the
species. Reduced habitat quality, as
reflected in unmet LHA objectives is
likely to negatively impact Gunnison
sage-grouse, particularly nesting and
early brood-rearing habitat, and chick
survival is one of the most important
factors in maintaining Gunnison sagegrouse population viability (GSRSC
2005, p. 173).
We know that grazing can have
negative impacts to sagebrush and
consequently to Gunnison sage-grouse
at local scales. Available data indicates
that impacts to sagebrush are occurring
on a significant portion of the range of
the species. Given the widespread
nature of grazing within the range of
Gunnison sage-grouse, the potential for
population-level impacts is highly
likely. Further, we expect grazing to
persist throughout the range of
Gunnison sage-grouse for the
foreseeable future. Effects of domestic
livestock grazing are likely being
exacerbated by intense browsing of
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woody species by wild ungulates in
portions of the Gunnison Basin. We
conclude that habitat degradation that
can result from improper grazing is a
significant threat to Gunnison sagegrouse now and in the foreseeable
future.
Nonrenewable Energy Development
Energy development on Federal (BLM
and USFS) lands is regulated by the
BLM and can contain conservation
measures for wildlife species (see Factor
D for a more thorough discussion). The
BLM (1999, p. 1) classified the area
encompassing all Gunnison sage-grouse
habitat for its gas and oil potential.
Three of the populations have areas
with high (San Miguel Basin, Monticello
group) or medium (Crawford) oil and
gas potential. San Miguel County, where
much oil and gas activity has occurred
in the last few years, ranked 9 out of 39
in Colorado counties producing natural
gas in 2009 (Colorado Oil and Gas
Conservation Commission 2010, p. 1)
and 29 of 39 in oil production in 2009
(Colorado Oil and Gas Conservation
commission 2010, p. 2).
Energy development impacts sagegrouse and sagebrush habitats through
direct habitat loss from well pad
construction, seismic surveys, roads,
powerlines and pipeline corridors, and
indirectly from noise, gaseous
emissions, changes in water availability
and quality, and human presence. The
interaction and intensity of effects could
cumulatively or individually lead to
habitat fragmentation (Suter 1978, pp. 613; Aldridge 1998, p. 12; Braun 1998,
pp. 144-148; Aldridge and Brigham
2003, p. 31; Knick et al. 2003, pp. 612,
619; Lyon and Anderson 2003, pp. 489490; Connelly et al. 2004, pp. 7-40 to 741; Holloran 2005, pp. 56-57; Holloran
2007 et al.,, pp. 18-19; Aldridge and
Boyce 2007, pp. 521-522; Walker et al.
2007a, pp. 2652-2653; Zou et al. 2006,
pp. 1039-1040; Doherty et al. 2008, p.
193; Leu and Hanser, in press, p. 28).
Increased human presence resulting
from oil and gas development can
impact sage-grouse either through
avoidance of suitable habitat, or
disruption of breeding activities (Braun
et al. 2002, pp. 4-5; Aldridge and
Brigham 2003, pp. 30-31; Aldridge and
Boyce 2007, p. 518; Doherty et al. 2008,
p. 194).
The development of oil and gas
resources requires surveys for
economically recoverable reserves,
construction of well pads and access
roads, subsequent drilling and
extraction, and transport of oil and gas,
typically through pipelines. Ancillary
facilities can include compressor
stations, pumping stations, electrical
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generators and powerlines (Connelly et
al. 2004, p. 7-39; BLM 2007, p. 2-110).
Surveys for recoverable resources occur
primarily through noisy seismic
exploration activities. These surveys can
result in the crushing of vegetation.
Well pads vary in size from 0.10 ha
(0.25 ac) for coal-bed natural gas wells
in areas of level topography to greater
than 7 ha (17.3 ac) for deep gas wells
and multiwell pads (Connelly et al.
2004, pp. 7-39; BLM 2007, pp. 2-123).
Pads for compressor stations require 5–
7 ha (12.4–17.3 ac) (Connelly et al. 2004,
pp. 7-39).
The amount of direct habitat loss
within an area is ultimately determined
by well densities and the associated loss
from ancillary facilities. Roads
associated with oil and gas development
were suggested to be the primary impact
to greater sage-grouse due to their
persistence and continued use even
after drilling and production ceased
(Lyon and Anderson 2003, p. 489).
Declines in male greater sage-grouse lek
attendance were reported within 3 km
(1.9 mi) of a well or haul road with a
traffic volume exceeding one vehicle per
day (Holloran 2005, p. 40). Because of
reasons discussed previously, we
believe the effects to Gunnison sagegrouse are similar to those observed in
greater sage-grouse. Sage-grouse also
may be at increased risk for collision
with vehicles simply due to the
increased traffic associated with oil and
gas activities (Aldridge 1998, p. 14; BLM
2003, p. 4-222).
Habitat fragmentation resulting from
oil and gas development infrastructure,
including access roads, may have
greater effects on sage-grouse than the
associated direct habitat losses. Energy
development and associated
infrastructure works cumulatively with
other human activity or development to
decrease available habitat and increase
fragmentation. Greater sage-grouse leks
had the lowest probability of persisting
(40–50 percent) in a landscape with less
than 30 percent sagebrush within 6.4
km (4 mi) of the lek (Walker et al. 2007a,
p. 2652). These probabilities were even
less in landscapes where energy
development also was a factor.
Nonrenewable Energy Development in
All Population Areas – Approximately
33 percent of the Gunnison Basin
population area ranked as low oil and
gas potential with the remainder having
no potential for oil and gas development
(GSRSC 2005, p. 130). Forty-three gas
wells occur on private lands within the
occupied range of the Gunnison sagegrouse. Of these, 27 wells occur in the
San Miguel population, 8 in the
Gunnison Basin population, 6 in the
Dove Creek group of the Monticello–
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59827
Dove Creek population, and 1 in each of
the Crawford and Cerro Summit–
Cimarron–Sims Mesa populations
(derived from Colorado Oil and Gas
Commission 2010, GIS dataset).
No federally leased lands exist within
the Gunnison Basin population area
(BLM and USFS 2010). The Monticello
group is in an area of high energy
potential (GSRSC 2005, p. 130);
however, less than two percent of the
population area contains Federal leases
upon which production is occurring,
and no producing leases occur in
currently occupied Gunnison sagegrouse habitat (BLM Geocommunicator,
2010). No oil and gas wells or
authorized Federal leases are within the
˜
Pınon Mesa population area (BLM 2009,
p. 1; BLM Geocommunicator), and no
potential for oil or gas exists in this area
except for a small area on the eastern
edge of the largest habitat block (BLM
1999, p. 1; GSRSC 2005, p. 130). The
Crawford population is in an area with
high to medium potential for oil and gas
development (GSRSC 2005, p. 130). A
single authorized Federal lease (BLM
Geocommunicator) constitutes less than
1 percent of the Crawford population
area.
Energy development is occurring
primarily in the San Miguel Basin
Gunnison sage-grouse population area
in Colorado. The entire San Miguel
Basin population area has high potential
for oil and gas development (GSRSC
2005, p. 130). Approximately 13 percent
of occupied habitat area within the San
Miguel Basin population has authorized
Federal leases; of that, production is
occurring on approximately 5 percent
(BLM National Integrated Lands System
(NILS) p. 1). Currently, 25 gas wells are
active within occupied habitat of the
San Miguel Basin, and an additional 18
active wells occur immediately adjacent
to occupied habitat (San Miguel County
2009, p. 1). All of these wells are in or
near the Dry Creek group. The exact
locations of any future drill sites are not
known, but because the area is small,
they will likely lie within 3 km (2 mi)
of one of only three leks in this group
(CDOW 2005a, p. 108).
Although the BLM has deferred
(temporarily withheld from recent lease
sales) oil and gas parcels nominated for
leasing in occupied Gunnison sagegrouse habitat in Colorado since 2005,
we expect energy development in the
San Miguel Basin on public and private
lands to continue over the next 20 years
based on the length of development and
production projects described in
existing project and management plans.
Current impacts from gas development
may exacerbate Gunnison sage-grouse
imperilment in the Dry Creek group
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because this area contains some of the
poorest habitat and smallest grouse
populations within the San Miguel
population (San Miguel Basin Gunnison
sage-grouse Working Group, 2009 pp. 28
and 36).
The San Miguel Basin population area
is the only area within the Gunnison
sage-grouse range with a high potential
for oil and gas development. However,
the immediate threat to Gunnison sagegrouse is limited because the BLM is
deferring leases until they can be
considered within Land Use Plans (BLM
2009, p. 78). We anticipate energy
development activities to continue over
the next 20 years. However, because
nonrenewable energy activities are
limited to a small portion of the range,
primarily the Dry Creek portion of the
San Miguel Basin population of
Gunnison sage-grouse, we do not
consider nonrenewable energy
development to be a significant threat to
the species.
Renewable Energy – Geothermal, Solar,
Wind
Geothermal energy production is
similar to oil and gas development in
that it requires surface exploration,
exploratory drilling, field development,
and plant construction and operation.
Wells are drilled to access the thermal
source and could take from 3 weeks to
2 months of drilling occurring on a
continuous basis (Suter 1978, p. 3),
which may cause disturbance to sagegrouse. The ultimate number of wells,
and therefore potential loss of habitat,
depends on the thermal output of the
source and expected production of the
plant (Suter 1978, p. 3). Pipelines are
needed to carry steam or superheated
liquids to the generating plant, which is
similar in size to a coal- or gas-fired
plant, resulting in further habitat
destruction and indirect disturbance.
Direct habitat loss occurs from well
pads, structures, roads, pipelines and
transmission lines, and impacts would
be similar to those described previously
for oil and gas development. The
development of geothermal energy
requires intensive human activity
during field development and operation.
Geothermal development could cause
toxic gas release. The type and effect of
these gases depends on the geological
formation in which drilling occurs
(Suter 1978, pp. 7-9). The amount of
water necessary for drilling and
condenser cooling may be high. Local
water depletions may be a concern if
such depletions result in the loss of
brood-rearing habitat.
Renewable Energy in the Gunnison
Basin Population Area – Approximately
87 percent of the occupied range of
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Gunnison sage-grouse is within a region
of known geothermal potential (BLM
Geocommunicator 2010, p. 1). We were
unable to find any information on the
presence of active geothermal energy
generation facilities; however, we are
aware of three current applications for
geothermal leases within the range of
Gunnison sage-grouse. All of the
applications are located in the same
general vicinity on private, BLM, USFS,
and Colorado State Land Board lands
near Tomichi Dome and Waunita Hot
Springs in southeastern Gunnison
County. The cumulative area of the
geothermal lease application parcels is
approximately 4,061 ha (10,035 ac), of
which approximately 3,802 ha (9,395
ac) is occupied Gunnison sage-grouse
habitat, or approximately 2 percent of
the Gunnison Basin population area.
One active lek and two inactive leks are
located within the lease application
parcels. In addition, six active leks and
four inactive leks are within 6.4 km (4
mi) of the lease application parcels
indicating that over 80 percent of
Gunnison sage-grouse seasonal use
occurs within the area associated with
these leks (GSRSC 2005, p. J-4). There
are 74 active leks in the Gunnison Basin
population, so approximately 10 percent
of active leks may be affected. A
significant amount of high-quality
Gunnison sage-grouse nesting habitat
exists on and near the lease application
parcels (Aldridge et al. 2010, in press).
This potential geothermal development
would likely negatively impact
Gunnison sage-grouse through the direct
loss of habitat and the functional loss of
habitat resulting from increased human
activity in the area; however, we cannot
determine the potential extent of the
impact at this time because the size and
location of potential geothermal energy
generation infrastructure and potential
resource protection conditions are
unknown at this time.
Renewable Energy in All Other
Population Areas – We could find no
information on the presence of existing,
pending, or authorized wind energy
sites, solar energy sites, nor any solar
energy study areas within the range of
Gunnison sage-grouse. A 388-ha (960ac) wind energy generation facility is
authorized on BLM lands in San Juan
County, UT. However, the authorized
facility is approximately 12.9 km (8 mi)
from the nearest lek in the Monticello
group of the Monticello–Dove Creek
Gunnison sage-grouse population.
Therefore, we conclude that wind and
solar energy development are not a
significant threat to the Gunnison sagegrouse and we do not expect these
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activities to become significant threats
in the foreseeable future.
The only existing or proposed
renewable energy project we are aware
of is located in the Gunnison Basin. A
portion of the Gunnison Basin
population will likely be adversely
affected by proposed geothermal
development if it is implemented.
Because of the current preliminary
status of geothermal development, we
lack the specific project details to
evaluate the extent to which this
activity will affect the population’s
overall viability. Therefore, we do not
consider renewable energy development
to be a threat to the Gunnison sagegrouse at this time. Geothermal energy
development could become a future
threat to the species, but we do not
know to what extent future geothermal
energy development will occur. Future
geothermal development could be
encouraged by a new Colorado State
law, signed April 30, 2010, that will
facilitate streamlining of the State
permitting process.
Summary of Nonrenewable and
Renewable Energy Development
The San Miguel Basin population area
is the only area within the Gunnison
sage-grouse range with a high potential
for oil and gas development. However,
the immediate threat to Gunnison sagegrouse is limited because the BLM is
temporarily deferring leases until they
can be considered within Land Use
Plans. We anticipate energy
development activities to continue over
the next 20 years. Although we
recognize that the Dry Creek portion of
the San Miguel Basin population may be
impacted by nonrenewable energy
development, we do not consider
nonrenewable energy development to be
a significant threat to the species now or
in the foreseeable future, because its
current and anticipated extent is limited
throughout the range of Gunnison sagegrouse. Similarly, we do not consider
renewable energy development to be a
significant threat to Gunnison sagegrouse now or in the foreseeable future.
However, geothermal energy
development could increase in the
future and could (depending on the
level of development and minimization
and mitigation measures) substantially
influence the overall long-term viability
of the Gunnison Basin population.
Climate Change
According to the Intergovernmental
Panel on Climate Change (IPCC),
‘‘Warming of the climate system in
recent decades is unequivocal, as is now
evident from observations of increases
in global average air and ocean
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temperatures, widespread melting of
snow and ice, and rising global sea
level’’ (IPCC 2007, p. 1). Average
Northern Hemisphere temperatures
during the second half of the 20th
century were very likely higher than
during any other 50–year period in the
last 500 years and likely the highest in
at least the past 1,300 years (IPCC 2007,
p. 30). Over the past 50 years cold days,
cold nights, and frosts have become less
frequent over most land areas, and hot
days and hot nights have become more
frequent. Heat waves have become more
frequent over most land areas, and the
frequency of heavy precipitation events
has increased over most areas (IPCC
2007, p. 30). For the southwestern
region of the United States, including
western Colorado, warming is occurring
more rapidly than elsewhere in the
country (Karl et al. 2009, p. 129).
Annual average temperature in westcentral Colorado increased 3.6 °C (2 °F)
over the past 30 years, but high
variability in annual precipitation
precludes the detection of long-term
trends (Ray et al. 2008, p. 5).
Under high emission scenarios, future
projections for the southwestern United
States show increased probability of
drought (Karl et al. 2009, pp. 129-134)
and the number of days over 32 °C (90
°F) could double by the end of the
century (Karl et al. 2009, p. 34). Climate
models predict annual temperature
increase of approximately 2.2 °C (4 °F)
in the southwest by 2050, with summers
warming more than winters (Ray et al.
2008, p. 29). Projections also show
declines in snowpack across the West,
with the most dramatic declines at
lower elevations (below 2,500 m (8,200
ft)) (Ray et al., p. 29).
Localized climate projections are
problematic for mountainous areas
because current global climate models
are unable to capture this topographic
variability at local or regional scales
(Ray et al. 2008, pp. 7, 20). To obtain
climate projections specific to the range
of Gunnison sage-grouse, we requested
a statistically downscaled model from
the National Center for Atmospheric
Research for a region covering western
Colorado. The resulting projections
indicate the highest probability scenario
is that average summer (June through
September) temperature could increase
by 2.8 °C (5.1 °F), and average winter
(October through March) temperature
could increase by 2.2 °C (4.0 °F) by 2050
(University Corporation for
Atmospheric Research (UCAR) 2009,
pp. 1-15). Annual mean precipitation
projections for Colorado are unclear;
however, multi-model averages show a
shift towards increased winter
precipitation and decreased spring and
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summer precipitation (Ray et al. 2008,
p. 34; Karl et al. 2009, p. 30). Similarly,
the multi-model averages show the
highest probability of a five percent
increase in average winter precipitation
and a five percent decrease in average
spring-summer precipitation in 2050
(UCAR 2009, p. 15).
While it is unclear at this time
whether or not the year 2050 predicted
changes in precipitation and
temperature will be of significant
magnitude to alter sagebrush plant
community composition and dynamics,
we believe climate change is likely to
alter fire frequency, community
assemblages, and the ability of
nonnative species to proliferate.
Increasing temperature as well as
changes in the timing and amount of
precipitation will alter the competitive
advantage among plant species (Miller
et al. in press, p. 44), and may shift
individual species and ecosystem
distributions (Bachelet et al. 2001, p.
174). For sagebrush, spring and summer
precipitation comprises the majority of
the moisture available to the species;
thus, the interaction between reduced
precipitation in the spring-summer
growing season and increased summer
temperatures will likely decrease
growth of mountain big sagebrush
(Artemisia tridentata ssp. vaseyana).
This could result in a significant longterm reduction in the distribution of
sagebrush communities (Miller et al. in
press, pp. 41-45). In the Gunnison
Basin, increased summer temperature
was strongly correlated with reduced
growth of mountain big sagebrush
(Poore et al. 2009, p. 558). Based on
these results and the likelihood of
increased winter precipitation falling as
rain rather than snow, Poore et al. (2009,
p. 559) predict decreased growth of
mountain big sagebrush, particularly at
the lower elevation limit of the species.
Because Gunnison sage-grouse are
sagebrush obligates, loss of sagebrush
would result in a reduction of suitable
habitat and negatively impact the
species. The interaction of climate
change with other stressors likely has
impacted and will impact the sagebrush
steppe ecosystem within which
Gunnison sage-grouse occur.
Temperature increases may increase
the competitive advantage of cheatgrass
in higher elevation areas where its
current distribution is limited (Miller et
al. in press, p. 47). Decreased summer
precipitation reduces the competitive
advantage of summer perennial grasses,
reduces sagebrush cover, and
subsequently increases the likelihood of
cheatgrass invasion (Prevey et al. 2009,
p. 11). This impact could increase the
susceptibility of areas within Gunnison
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59829
sage-grouse range to cheatgrass invasion
(Bradley 2009, p. 204), which would
reduce the overall cover of native
vegetation, reduce habitat quality, and
potentially decrease fire return
intervals, all of which would negatively
affect the species.
Summary of Climate Change
Climate change predictions are based
on models with assumptions, and there
are uncertainties regarding the
magnitude of associated climate change
parameters such as the amount and
timing of precipitation and seasonal
temperature changes. There is also
uncertainty as to the magnitude of
effects of predicted climate parameters
on sagebrush plant community
dynamics. These factors make it
difficult to predict the effects of climate
change on Gunnison sage-grouse. We
recognize that climate change has the
potential to alter Gunnison sage-grouse
habitat by facilitating an increase in the
distribution of cheatgrass and
concurrently increase the potential for
wildfires, which would have negative
effects on Gunnison sage-grouse.
However, based on the best available
information on climate change
projections into the next 40 years, we do
not consider climate change to be a
significant threat to the Gunnison sagegrouse at this time. Existing data
indicates that climate change has the
potential to alter changes in the
distribution and extent of cheatgrass
and sagebrush and associated fire
frequencies and therefore is likely to
become an increasingly important factor
affecting Gunnison sage-grouse and its
habitat in the foreseeable future.
Summary of Factor A
Gunnison sage-grouse require large,
contiguous areas of sagebrush for longterm persistence, and thus are affected
by factors that occur at the landscape
scale. Broad-scale characteristics within
surrounding landscapes influence
habitat selection, and adult Gunnison
sage-grouse exhibit a high fidelity to all
seasonal habitats, resulting in low
adaptability to habitat changes.
Fragmentation of sagebrush habitats has
been cited as a primary cause of the
decline of Gunnison and greater sagegrouse populations (Patterson 1952, pp.
192-193; Connelly and Braun 1997, p. 4;
Braun 1998, p. 140; Johnson and Braun
1999, p. 78; Connelly et al. 2000a, p.
975; Miller and Eddleman 2000, p. 1;
Schroeder and Baydack 2001, p. 29;
Johnsgard 2002, p. 108; Aldridge and
Brigham 2003, p. 25; Beck et al. 2003,
p. 203; Pedersen et al. 2003, pp. 23-24;
Connelly et al. 2004, p. 4-15; Schroeder
et al. 2004, p. 368; Leu et al. in press,
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p. 19). Documented negative effects of
fragmentation include reduced lek
persistence, lek attendance, population
recruitment, yearling and adult annual
survival, female nest site selection, and
nest initiation rates, as well as the loss
of leks and winter habitat (Holloran
2005, p. 49; Aldridge and Boyce 2007,
pp. 517-523; Walker et al. 2007a, pp.
2651-2652; Doherty et al. 2008, p. 194).
We examined several factors that
result in habitat loss and fragmentation.
Historically, losses of sagebrush habitats
occurred due to conversion for
agricultural croplands; however, this
trend has slowed or slightly reversed in
recent decades. Currently, direct and
functional loss of habitat due to
residential and road development in all
populations, including the largest
population in the Gunnison Basin, is the
principal threat to Gunnison sagegrouse. Functional habitat loss also
contributes to habitat fragmentation as
sage-grouse avoid areas due to human
activities, including noise, even when
sagebrush remains intact. The collective
disturbance from human activities
around residences and roads reduces
the effective habitat around these areas,
making them inhospitable to Gunnison
sage-grouse. Human populations are
increasing in Colorado and throughout
the range of Gunnison sage-grouse. This
trend is expected to continue at least
through 2050. The resulting habitat loss
and fragmentation will continue to
negatively affect Gunnison sage-grouse
and its habitat.
Other threats from human
infrastructure such as fences and
powerlines may not individually
threaten the Gunnison sage-grouse.
However, the cumulative presence of all
these features, particularly when
considered in conjunction with
residential and road development, does
constitute a significant threat to
Gunnison sage-grouse as they
collectively contribute to habitat loss
and fragmentation. This impact is
particularly of consequence in light of
the decreases in Gunnison sage-grouse
population sizes observed in the six
smallest populations. These
infrastructure components are
associated with overall increases in
human populations and thus we expect
them to continue to increase in the
foreseeable future.
Several issues discussed above, such
as fire, invasive species, and climate
change, may not individually threaten
the Gunnison sage-grouse. However, the
documented synergy among these issues
result in a high likelihood that they will
threaten the species in the future.
Nonnative invasive plants, including
cheatgrass and other noxious weeds,
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continue to expand their range,
facilitated by ground disturbances such
as fire, grazing, and human
infrastructure. Invasive plants
negatively impact Gunnison sage-grouse
primarily by reducing or eliminating
native vegetation that sage-grouse
require for food and cover, resulting in
habitat loss (both direct and functional)
and fragmentation. Cheatgrass is present
at varying levels in nearly all Gunnison
sage-grouse population areas, but there
has not yet been a demonstrated change
in fire cycle in the range of Gunnison
sage-grouse. However, climate change
may alter the range of invasive plants,
intensifying the proliferation of invasive
plants to the point that they and their
effects on Gunnison sage-grouse habitat
will likely become a threat to the
species. Even with aggressive
treatments, invasive plants will persist
and will likely continue to spread
throughout the range of Gunnison sagegrouse in the foreseeable future.
Livestock management has the
potential to degrade sage-grouse habitat
at local scales by causing the loss of
nesting cover and decreases in native
vegetation, and by increasing the
probability of incursion of invasive
plants. Given the widespread nature of
grazing within the range of Gunnison
sage-grouse, the potential for
population-level impacts is highly
likely. Effects of domestic livestock
grazing are likely being exacerbated by
intense browsing of woody species by
wild ungulates in portions of the
Gunnison Basin. We conclude that
habitat degradation that can result from
improper grazing is a significant threat
to Gunnison sage-grouse now and in the
foreseeable future.
Threats identified above, particularly
residential development and associated
infrastructure such as fences, roads, and
powerlines, are cumulatively causing
significant habitat fragmentation that is
negatively affecting Gunnison sagegrouse. We have evaluated the best
available scientific information
available on the present or threatened
destruction, modification or curtailment
of the Gunnison sage-grouse’s habitat or
range. Based on the current and
anticipated habitat threats identified
above, and their cumulative effects as
they contribute to the overall
fragmentation of Gunnison sage-grouse
habitat, we have determined that the
present or threatened destruction,
modification, or curtailment of
Gunnison sage-grouse habitat poses a
significant threat to the species
throughout its range.
The species is being impacted by
several other factors, but their
significance is not at a level that they
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cause the species to become threatened
or endangered in the foreseeable future.
We do not consider nonrenewable
energy development to be a significant
threat to the species because its current
and anticipated extent is limited
throughout the range of Gunnison sagegrouse. Similarly, we do not consider
renewable energy development to be a
significant threat to the Gunnison sagegrouse at this time. However,
geothermal energy development could
˜
increase in the future. Pınon-juniper
encroachment does not pose a
significant threat to Gunnison sagegrouse at a population or rangewide
level because of its limited distribution
throughout the range of Gunnison sagegrouse and the observed effectiveness of
treatment projects.
A review of a database compiled by
the CDOW that included local, State,
and Federal ongoing and proposed
Gunnison sage-grouse conservation
actions (CDOW 2009c, entire) revealed a
total of 224 individual conservation
efforts. Of these 224 efforts, a total of
165 efforts have been completed and
were focused on habitat improvement or
protection. These efforts resulted in the
treatment of 9,324 ha (23,041 ac), or
approximately 2.5 percent of occupied
Gunnison sage-grouse habitat. A
monitoring component was included in
75 (45 percent) of these 165 efforts,
although we do not have information on
the overall effectiveness of these efforts.
Given the limited collective extent of
these efforts, they do not ameliorate the
effects of habitat fragmentation at a
sufficient scale range-wide to effectively
reduce or eliminate the most significant
threats to the species. We recognize
ongoing and proposed conservation
efforts by all entities across the range of
the Gunnison sage-grouse, and all
parties should be commended for their
conservation efforts. Our review of
conservation efforts indicates that the
measures identified are not adequate to
address the primary threat of habitat
fragmentation at this time in a manner
that effectively reduces or eliminates the
most significant contributors (e.g.,
residential development) to this threat.
All of the conservation efforts are
limited in size and the measures
provided to us were simply not
implemented at the scale (even when
considered cumulatively) that would be
required to effectively reduce the threats
to the species across its range. Although
the ongoing conservation efforts are a
positive step toward the conservation of
the Gunnison sage-grouse, and some
have likely reduced the severity of some
˜
threats to the species (e.g., Pınonjuniper invasion), on the whole we find
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that the conservation efforts in place at
this time are not sufficient to offset the
degree of threat posed to the species by
the present and threatened destruction,
modification, or curtailment of its
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B. Overutilization for Commercial,
Recreational, Scientific, or Educational
Purposes
Hunting
Hunting for Gunnison sage-grouse
does not currently occur. Hunting was
eliminated in the Gunnison Basin in
2000 due to concerns with meeting
Gunnison sage-grouse population
objectives (CSGWG 1997, p. 66).
Hunting has not occurred in the other
Colorado populations of Gunnison sage˜
grouse since 1995 when the Pınon Mesa
area was closed (GSRSC 2005, p. 122).
Utah has not allowed hunting of
Gunnison sage-grouse since 1989
(GSRSC 2005, p. 82).
Both Colorado and Utah will only
consider hunting of Gunnison sagegrouse if populations can be sustained
(GSRSC 2005, pp. 5, 8, 229). The
Gunnison Basin Plan calls for a
minimum population of 500 males
counted on leks before hunting would
occur again (CSGWG 1997, p. 66). The
minimum population level has been
exceeded in all years since 1996, except
2003 and 2004 (CDOW 2009d, p. 18-19).
However, the sensitive State regulatory
status and potential political
ramifications of hunting the species has
precluded the States from opening a
hunting season. If hunting does ever
occur again, harvest will likely be
restricted to only 5 to 10 percent of the
fall population, and will be structured
to limit harvest of females to the extent
possible (GSRSC 2005, p. 229).
However, the ability of these measures
to be implemented is in question, as
adequate means to estimate fall
population size have not been
developed (Reese and Connelly in press,
p. 21) and limiting female harvest may
not be possible (WGFD 2004, p. 4;
WGFD 2006, pp. 5, 7). Despite these
questions, we believe that the low level
of hunting that could be allowed in the
future would not be a significant threat
to the Gunnison sage-grouse.
One sage-grouse was known to be
illegally harvested in 2001 in the
Poncha Pass population (Nehring 2010,
pers. comm.), but based on the best
available information we do not believe
that illegal harvest has contributed to
Gunnison sage-grouse population
declines in either Colorado or Utah. We
do not anticipate hunting to be opened
in the Gunnison Basin or smaller
populations for many years, if ever.
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Consequently, we do not consider
hunting to be a significant threat to the
species now or in the foreseeable future.
Lek Viewing
The Gunnison sage-grouse was
designated as a new species in 2000
(American Ornithologists’ Union 2000,
pp. 847-858), which has prompted
increased interest by bird watchers to
view the species on their leks (Pfister
2010, pers. comm.). Daily human
disturbances on sage-grouse leks could
cause a reduction in mating, and some
reduction in total production (Call and
Maser 1985, p. 19). Human disturbance,
particularly if additive to disturbance by
predators, could reduce the time a lek
is active, as well as reduce its size by
lowering male attendance (Boyko et al.
2004, in GSRSC 2005, p. 125). Smaller
lek sizes have been hypothesized to be
less attractive to females, thereby
conceivably reducing the numbers of
females mating. Disturbance during the
peak of mating also could result in some
females not breeding (GSRSC 2005, p.
125). Furthermore, disturbance from lek
viewing might affect nesting habitat
selection by females (GSRSC 2005, p.
126), as leks are typically close to areas
in which females nest. If females move
to poorer quality habitat farther away
from disturbed leks, nest success could
decline. If chronic disturbance causes
sage-grouse to move to a new lek site
away from preferred and presumably
higher quality areas, both survival and
nest success could decline. Whether any
or all of these have significant
population effects would depend on
timing and degree of disturbance
(GSRSC 2005, p. 126).
Throughout the range of Gunnison
sage-grouse, public viewing of leks is
limited by a general lack of knowledge
in the public of lek locations, seasonal
road closures in some areas, and
difficulty in accessing many leks.
Furthermore, 52 of 109 active Gunnison
sage-grouse leks occur on private lands,
which further limits access by the
public. The BLM closed a lek in the
Gunnison Basin to viewing in the late
1990s due to declining population
counts, which were perceived as
resulting from recreational viewing,
although no scientific studies were
conducted (BLM 2005a, p. 13; GSRSC
2005, pp. 124, 126). The Waunita lek
east of Gunnison is the only lek in
Colorado designated by the CDOW for
public viewing (CDOW 2009a, p. 86).
Since 1998, a comparison of male
counts on the Waunita lek versus male
counts on other leks in the Doyleville
zone show that the Waunita lek’s male
counts generally follow the same trend
as the others (CDOW 2009d, pp. 31-32).
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In fact, in 2008 and 2009 the Waunita
lek increased in the number of males
counted along with three other leks,
while seven leks decreased in the
Doyleville zone (CDOW 2009d, pp. 3132). These data suggest that lek viewing
on the Waunita lek has not impacted the
Gunnison sage-grouse. Two lek-viewing
tours per year are organized and led by
UDWR on a privately owned lek in the
Monticello population. The lek declined
in males counted in 2009, but 2007 and
2008 had the highest counts for several
years, suggesting that lek viewing is also
not impacting that lek. Data collected by
CDOW on greater sage-grouse viewing
leks also indicates that controlled lek
visitation has not impacted greater sagegrouse at the viewed leks (GSRSC 2005,
p. 124).
A lek viewing protocol has been
developed and has largely been
followed on the Waunita lek, likely
reducing impacts to sage-grouse using
the lek (GSRSC 2005, p. 125). During
2004-2009, the percentage of
individuals or groups of people in
vehicles following the Waunita lek
viewing protocol in the Gunnison Basin
ranged from 71–92 percent (CDOW
2009a, p. 86, 87; Magee et al. 2009, p.
7, 10). Violations of the protocol, such
as showing up after the sage-grouse
started to display and creating noise,
caused one or more sage-grouse to flush
from the lek (CDOW 2009a, pp. 86, 87).
Despite the protocol violations, the
percentage of days from 2004 to 2009
that grouse were flushed by humans was
relatively low, ranging from 2.5 percent
to 5.4 percent (Magee et al. 2009, p.10).
Nonetheless, the lek viewing protocol is
currently being revised to make it more
stringent and to include considerations
for photography, research, and
education related viewing (CDOW
2009a, p. 86). Maintenance of this
protocol should preclude lek viewing
from becoming a threat to this lek.
The CDOW and UDWR will continue
to coordinate and implement lek counts
to determine population levels. We
expect annual lek viewing and lek
counts to continue indefinitely.
However, all leks counted will receive
lower disturbance from counters than
the Waunita lek received from public
viewing, so we do not consider lek
counts and viewing a threat to the
Gunnison sage-grouse now or in the
foreseeable future.
Scientific Research
Gunnison sage-grouse have been the
subject of scientific research studies,
some of which included the capture and
handling of the species. Most of the
research has been conducted in the
Gunnison Basin population, San Miguel
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Basin population, and Monticello
portion of the Monticello–Dove Creek
population. Between zero and seven
percent mortality of handled adults or
juveniles and chicks has occurred
during recent Gunnison sage-grouse
studies where trapping and radiotagging was done (Apa 2004, p. 19;
Childers 2009, p. 14; Lupis 2005, p. 26;
San Miguel Basin Working Group 2009,
p. A-10). Additionally, one radio-tagged
hen was flushed off a nest during
subsequent monitoring and did not
return after the second day, resulting in
loss of 10 eggs (Ward 2007, p. 52). The
CDOW does not believe that these losses
or disturbance have any significant
impacts on the sage-grouse (CDOW
2009a, p. 29).
Some of the radio-tagged sage-grouse
have been translocated from the
Gunnison Basin to other populations.
Over a 5–year period (2000–2002 and
2006–2007), 68 sage-grouse were
translocated from the Gunnison Basin to
the Poncha Pass and San Miguel Basin
populations (CDOW 2009a, p. 9). These
experimental translocations were
conducted to determine translocation
techniques and survivorship in order to
increase both size of the receiving
populations and to increase genetic
diversity in populations outside of the
Gunnison Basin. However, the
translocated grouse experienced 40–50
percent mortality within the first year
after release, which is double the
average annual mortality of nontranslocated sage-grouse (CDOW 2009a,
p. 9). Greater sage-grouse translocations
have not appeared to fare any better.
Over 7,200 greater sage-grouse were
translocated between 1933 and 1990,
but only five percent of the
translocation efforts were considered to
be successful in producing sustained,
resident populations at the translocation
sites (Reese and Connelly 1997, pp. 235238, 240). More recent translocations
from 2003 to 2005 into Strawberry
Valley, Utah, resulted in a 40 percent
annual mortality rate (Baxter et al. 2008,
p. 182). We believe the lack of success
of translocations found in greater sagegrouse is applicable to Gunnison sagegrouse since the two species exhibit
similar behavior and life-history traits,
and are managed accordingly.
Because the survival rate for
translocated sage-grouse has not been as
high as desired, the CDOW started a
captive-rearing program in 2009 to
study whether techniques can be
developed to captively rear and release
Gunnison sage-grouse and enhance their
survival (CDOW 2009a, pp. 9-12). The
Gunnison Sage-grouse Rangewide
Steering Committee conducted a review
of captive-rearing attempts for both
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greater sage-grouse and other
gallinaceous birds and concluded that
survival will be very low, unless
innovative strategies are developed and
tested (GSRSC 2005, pp. 181-183).
However, greater sage-grouse have been
captively reared, and survival of
released chicks was similar to that of
wild chicks (CDOW 2009a, p. 10).
Consequently, the CDOW decided to try
captive rearing. Of 40 Gunnison sagegrouse eggs taken from the wild, only 11
chicks (about 25 percent) survived
through October 2009. Although chick
survival was low, the CDOW believes
they have gained valuable knowledge on
Gunnison sage-grouse rearing
techniques. As techniques improve, the
CDOW intends to develop a captivebreeding manual (CDOW 2009a, p. 11).
Although adults or juveniles have been
captured and moved out of the
Gunnison Basin, as well as eggs, the
removal of the grouse only accounts for
a very small percentage of the total
population of the Gunnison Basin sagegrouse population (about 1 percent).
The CDOW has a policy regarding
trapping, handling, and marking
techniques approved by their Animal
Use and Care Committee (San Miguel
Basin Working Group 2009, p. A-10,
Childers 2009, p. 13). Evaluation of
research projects by the Animal Use and
Care Committee and improvement of
trapping, handling, and marking
techniques over the last several years
has resulted in fewer mortalities and
injuries. In fact, in the San Miguel
Basin, researchers have handled over
200 sage-grouse with no trapping
mortalities (San Miguel Basin Working
Group (SMBWG) 2009, p. A-10). The
CDOW has also drafted a sage-grouse
trapping and handling protocol, which
is required training for people handling
Gunnison sage-grouse, to minimize
mortality and injury of the birds (CDOW
2002, pp. 1-4 in SMBWG 2009, pp. A22-A-25). Injury and mortality does
occasionally occur from trapping,
handling, marking, and flushing off
nests. However, research-related
mortality is typically below three
percent of handled birds and equates to
one half of one percent or less of annual
population estimates (Apa 2004, p. 19;
Childers 2009, p. 14; Lupis 2005, p. 26;
San Miguel Basin Working Group 2009,
p. A-10).
Research needs may gradually
dwindle over the years but annual or
occasional research is expected to occur
for at least 50 years constituting the
foreseeable future for this potential
threat. Short-term disturbance effects to
individuals occur as does injury and
mortality, but we do not believe these
effects cause a threat to the Gunnison
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sage-grouse population as a whole.
Based on the available information, we
believe scientific research on Gunnison
sage-grouse has a relatively minor
impact that does not rise to the level of
a threat to the species now or is it
expected to do so in the foreseeable
future.
Summary of Factor B
We have no evidence suggesting that
hunting, when it was legal, resulted in
overutilization of Gunnison sage-grouse.
If hunting is allowed again, future
hunting may result in additive mortality
due to habitat degradation and
fragmentation, despite harvest level
restrictions and management intended
to limit impacts to hens. Nonetheless,
we do not expect hunting to be
reinstated in the foreseeable future.
Illegal hunting has been documented
only once in Colorado and is not
considered a threat to the species. Lek
viewing has not affected the Gunnison
sage-grouse, and lek viewing protocols
designed to reduce disturbance have
generally been followed. CDOW is
currently revising their lek viewing
protocol to make it more stringent and
to include considerations for
photography, research, and educationrelated viewing. Mortality from
scientific research is low (2 percent) and
is not considered a threat. We know of
no overutilization for commercial or
educational purposes. Thus, based on
the best scientific and commercial data
available, we have concluded that
overutilization for commercial,
recreational, scientific, or educational
purposes does not constitute a
significant threat to the Gunnison sagegrouse.
C. Disease or Predation
Disease
No research has been published about
the types or pathology of diseases in
Gunnison sage-grouse. However,
multiple bacterial and parasitic diseases
have been documented in greater sagegrouse (Patterson 1952, pp. 71-72;
Schroeder et al. 1999, p. 14, 27). Some
early studies have suggested that greater
sage-grouse populations are adversely
affected by parasitic infections
(Batterson and Morse 1948, p. 22).
However, the role of parasites or
infectious diseases in population
declines of greater sage-grouse is
unknown based on the few systematic
surveys conducted (Connelly et al.
2004, p. 10-3). No parasites have been
documented to cause mortality in
Gunnison sage-grouse, but the
protozoan, Eimeria spp., which causes
coccidiosis, has been reported to cause
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death in greater sage-grouse (Connelly et
al. 2004, p. 10-4). Infections tend to be
localized to specific geographic areas,
and no cases of greater sage-grouse
mortality resulting from coccidiosis
have been documented since the early
1960s (Connelly et al. 2004, p. 10-4).
Parasites have been implicated in
greater sage-grouse mate selection, with
potentially subsequent effects on the
genetic diversity of this species (Boyce
1990, p.263; Deibert 1995, p. 38). These
relationships may be important to the
long-term ecology of greater sage-grouse,
but they have not been shown to be
significant to the immediate status of
populations (Connelly et al. 2004, p. 106). Although diseases and parasites have
been suggested to affect isolated sagegrouse populations (Connelly et al.
2004, p. 10-3), we have no evidence
indicating that parasitic diseases are a
threat to Gunnison sage-grouse
populations.
Greater sage-grouse are subject to a
variety of bacterial, fungal, and viral
pathogens. The bacterium Salmonella
sp. has caused a single documented
mortality in the greater sage-grouse and
studies have shown that infection rates
in wild birds are low (Connelly et al.
2004, p. 10-7). The bacteria are
apparently contracted through exposure
to contaminated water supplies around
livestock stock tanks (Connelly et al.
2004, p. 10-7). Other bacteria found in
greater sage-grouse include Escherichia
coli, botulism (Clostridium spp.), avian
tuberculosis (Mycobacterium avium),
and avian cholera (Pasteurella
multocida). These bacteria have never
been identified as a cause of mortality
in greater sage-grouse and the risk of
exposure and hence, population effects,
is low (Connelly et al. 2004, p. 10-7 to
10-8). We have no reason to expect that
mortality and exposure risk are different
in Gunnison sage-grouse; therefore, we
do not believe these bacteria to be a
threat to the species.
West Nile virus was introduced into
the northeastern United States in 1999
and has subsequently spread across
North America (Marra et al. 2004,
p.394). In sagebrush habitats, West Nile
virus transmission is primarily
regulated by environmental factors,
including temperature, precipitation,
and anthropogenic water sources, such
as stock ponds and coal-bed methane
ponds that support the mosquito vectors
(Reisen et al. 2006, p. 309; Walker and
Naugle in press, pp. 10-12). The virus
persists largely within a mosquito-birdmosquito infection cycle (McLean 2006,
p. 45). However, direct bird-to-bird
transmission of the virus has been
documented in several species (McLean
2006, pp. 54, 59) including the greater
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sage-grouse (Walker and Naugle in
press, p. 13; Cornish 2009, pers. comm.).
The frequency of direct transmission
has not been determined (McLean 2006,
p. 54). Cold ambient temperatures
preclude mosquito activity and virus
amplification, so transmission to and in
sage-grouse is limited to the summer
(mid-May to mid-September) (Naugle et
al. 2005, p. 620; Zou et al. 2007, p. 4),
with a peak in July and August (Walker
and Naugle in press, p. 10). Reduced
and delayed West Nile virus
transmission in sage-grouse has
occurred in years with lower summer
temperatures (Naugle et al. 2005, p. 621;
Walker et al. 2007b, p. 694). In nonsagebrush ecosystems, high
temperatures associated with drought
conditions increase West Nile virus
transmission by allowing for more rapid
larval mosquito development and
shorter virus incubation periods
(Shaman et al. 2005, p. 134; Walker and
Naugle in press, p. 11). Additional
details on the impacts of West Nile virus
on greater sage-grouse can be found in
our recent finding (75 FR 13910; March
23, 2010).
Greater sage-grouse congregate in
mesic habitats in the mid-late summer
(Connelly et al. 2000, p. 971), thereby
increasing their risk of exposure to
mosquitoes. If West Nile virus outbreaks
coincide with drought conditions that
aggregate birds in habitat near water
sources, the risk of exposure to West
Nile virus will be elevated (Walker and
Naugle in press, p. 11). Greater sagegrouse inhabiting higher elevation sites
in summer (similar to the northern
portion of the Gunnison Basin) are
likely less vulnerable to contracting
West Nile virus than birds at lower
elevation (similar to Dry Creek Basin of
the San Miguel population) as ambient
temperatures are typically cooler
(Walker and Naugle in press, p. 11).
West Nile Virus has caused
population declines in wild bird
populations on the local and regional
scale (Walker and Naugle in press, p. 7)
and has been shown to affect survival
rates of greater sage-grouse (Naugle et al.
2004, p. 710; Naugle et al. 2005, p. 616).
Experimental results, combined with
field data, suggest that a widespread
West Nile virus infection has negatively
affected greater sage-grouse (Naugle et
al. 2004, p. 711; Naugle et al. 2005, p.
616). Summer habitat requirements of
sage-grouse potentially increase their
exposure to West Nile virus. Greater
sage-grouse are considered to have a
high susceptibility to West Nile virus,
with resultant high levels of mortality
(Clark et al. 2006, p. 19; McLean 2006,
p. 54). Data collected on greater sagegrouse suggest that sage-grouse do not
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develop a resistance to the disease, and
death is certain once an individual is
exposed (Clark et al. 2006, p. 18).
To date, West Nile virus has not been
documented in Gunnison sage-grouse
despite the presence of West Nile viruspositive mosquitoes in nearly all
counties throughout their range
(Colorado Department of Public Health
2004, pp. 1-5; U.S. Centers for Disease
Control and Prevention 2004, entire).
We do not know whether this is a result
of the small number of birds that are
marked, the relatively few birds that
exist in the wild, or unsuitable
conditions in Gunnison sage-grouse
habitat for the virus to become virulent.
West Nile virus activity within the range
of Gunnison sage-grouse has been low
compared to other parts of Colorado and
the western United States. A total of 77
wild bird (other than Gunnison sagegrouse) deaths resulting from West Nile
virus have been confirmed from
counties within the occupied range of
Gunnison sage-grouse since 2002 when
reporting began in Colorado (USGS
2009, entire). Fifty-two (68 percent) of
these West-Nile-virus-caused bird
deaths were reported from Mesa County
˜
(where the Pınon Mesa population is
found). Only San Miguel, Dolores, and
Hinsdale Counties had no confirmed
avian mortalities resulting from West
Nile virus.
Walker and Naugle (in press, p. 27)
predict that West Nile virus outbreaks in
small, isolated, and genetically
depauperate populations could reduce
sage-grouse numbers below a threshold
from which recovery is unlikely because
of limited or nonexistent demographic
and genetic exchange from adjacent
populations. Thus, a West Nile virus
outbreak in any Gunnison sage-grouse
population, except perhaps the
Gunnison Basin population, could limit
the persistence of these populations.
Although West Nile virus is a
potential threat, the best available
information suggests that it is not
currently a significant threat to
Gunnison sage-grouse, since West Nile
virus has not been documented in
Gunnison sage-grouse despite the
presence of West Nile virus-positive
mosquitoes in nearly all counties
throughout their range. No other
diseases or parasitic infections are
considered to be threatening the
Gunnison sage-grouse at this time.
Predation
Predation is the most commonly
identified cause of direct mortality for
sage-grouse during all life stages
(Schroeder et al. 1999, p. 9; Connelly et
al. 2000b, p. 228; Connelly et al. in
press a, p. 23). However, sage-grouse
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have co-evolved with a variety of
predators, and their cryptic plumage
and behavioral adaptations have
allowed them to persist despite this
mortality factor (Schroeder et al. 1999,
p. 10; Coates 2008 p. 69; Coates and
Delehanty 2008, p. 635; Hagen in press,
p. 3). Until recently, little published
information has been available that
indicates predation is a limiting factor
for the greater sage-grouse (Connelly et
al. 2004, p. 10-1), particularly where
habitat quality has not been
compromised (Hagen in press, p. 3).
Although many predators will consume
sage-grouse, none specialize on the
species (Hagen in press, p. 5). Generalist
predators have the greatest effect on
ground-nesting birds because predator
numbers are independent of the density
of a single prey source since they can
switch to other prey sources when a
given prey source (e.g., Gunnison sagegrouse) is not abundant (Coates 2007, p.
4). We believe that the effects of
predation observed in greater sagegrouse are applicable to the effects
anticipated in Gunnison sage-grouse
since overall behavior and life-history
traits are similar for the two species.
Major predators of adult sage-grouse
include many species including golden
eagles (Aquila chrysaetos), red foxes
(Vulpes fulva), and bobcats (Felis rufus)
(Hartzler 1974, pp. 532-536; Schroeder
et al. 1999, pp. 10-11; Schroeder and
Baydack 2001, p. 25; Rowland and
Wisdom 2002, p. 14; Hagen in press, pp.
4-5). Juvenile sage-grouse also are killed
by many raptors as well as common
ravens (Corvus corax), badgers (Taxidea
taxus), red foxes, coyotes (Canis latrans)
and weasels (Mustela spp.) (Braun 1995,
entire; Schroeder et al. 1999, p. 10). Nest
predators include badgers, weasels,
coyotes, common ravens, American
crows (Corvus brachyrhyncos) and
magpies (Pica spp.), elk (Cervus
canadensis) (Holloran and Anderson
2003, p.309), and domestic cows (Bovus
spp.) (Coates et al. 2008, pp. 425-426).
Ground squirrels (Spermophilus spp.)
also have been identified as nest
predators (Patterson 1952, p. 107;
Schroeder et al. 1999, p. 10; Schroder
and Baydack 2001, p. 25), but recent
data show that they are physically
incapable of puncturing eggs (Holloran
and Anderson 2003, p. 309; Coates et al.
2008, p. 426; Hagen in press, p. 6).
Several other small mammals visited
sage-grouse nests in Nevada, but none
resulted in predation events (Coates et
al. 2008, p. 425). The most common
predators of Gunnison sage-grouse eggs
are weasels, ground squirrels, coyotes,
and corvids (Young 1994, p. 37). Most
raptor predation of sage-grouse is on
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juveniles and older age classes (GSRSC
2005, p. 135). Golden eagles were found
to be the dominant species recorded
perching on power poles in Utah in
Gunnison sage-grouse habitat (Prather
and Messmer 2009, p. 12). Twenty-two
and 40 percent of 111 adult mortalities
were the result of avian and mammalian
predation, respectively (Childers 2009,
p. 7). Twenty-five and 35 percent of 40
chick mortalities were caused by avian
and mammalian predation, respectively
(Childers 2009, p. 7). A causative agent
of mortality was not determined in the
remaining depredations observed in the
western portion of the Gunnison Basin
from 2000 to 2009 (Childers 2009, p. 7).
Adult male Gunnison sage-grouse are
very susceptible to predation while on
the lek (Schroeder et al. 1999, p. 10;
Schroeder and Baydack 2001, p. 25;
Hagen in press, p. 5), presumably
because they are conspicuous while
performing their mating displays.
Because leks are attended daily by
numerous grouse, predators also may be
attracted to these areas during the
breeding season (Braun 1995, p. 2).
Connelly et al. (2000b, p. 228) found
that among 40 radio-collared males, 83
percent of the mortality was due to
predation and 42 percent of those
mortalities occurred during the lekking
season (March through June). Adult
female greater sage-grouse are
susceptible to predators while on the
nest, but mortality rates are low (Hagen
in press, p. 6). Hens will abandon their
nest when disturbed by predators
(Patterson 1952, p. 110), likely reducing
this mortality (Hagen in press, p. 6).
Among 77 adult hens, 52 percent of the
mortality was due to predation and 52
percent of those mortalities occurred
between March and August, which
includes the nesting and brood-rearing
periods (Connelly et al. 2000b, p. 228).
Sage-grouse populations are likely more
sensitive to predation upon females
given the highly negative response of
Gunnison sage-grouse population
dynamics to adult female reproductive
success and chick mortality (GSRSC,
2005, p. 173). Predation of adult sagegrouse is low outside the lekking,
nesting, and brood-rearing season
(Connelly et al. 2000b, p. 230; Naugle et
al. 2004, p. 711; Moynahan et al. 2006,
p. 1536; Hagen in press, p. 6).
Estimates of predation rates on
juveniles are limited due to the
difficulties in studying this age class
(Aldridge and Boyce 2007, p. 509;
Hagen in press, p. 8). For greater sagegrouse, chick mortality from predation
ranged from 10 to 51 percent in 2002
and 2003 on three study sites in Oregon
(Gregg et al. 2003a, p. 15; 2003b, p. 17).
Mortality due to predation during the
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first few weeks after hatching was
estimated to be 82 percent (Gregg et al.
2007, p. 648). Survival of juveniles to
their first breeding season was estimated
to be low (10 percent). It is reasonable,
given the sources of adult mortality, to
assume that predation is a contributor to
the high juvenile mortality rates
(Crawford et al. 2004, p. 4).
Sage-grouse nests are subject to
varying levels of predation. Predation
can be total (all eggs destroyed) or
partial (one or more eggs destroyed).
However, hens abandon nests in either
case (Coates, 2007, p. 26). Gregg et al.
(1994, p. 164) reported that over a 3–
year period in Oregon, 106 of 124 nests
(84 percent) were preyed upon (Gregg et
al. 1994, p. 164). Patterson (1952, p.104)
reported nest predation rates of 41
percent in Wyoming. Holloran and
Anderson (2003, p. 309) reported a
predation rate of 12 percent (3 of 26) in
Wyoming. Moynahan et al. (2007, p.
1777) attributed 131 of 258 (54 percent)
nest failures to predation in Montana.
Studies have shown that re-nesting rates
are low in Gunnison sage-grouse
(Young, 1994, p. 44; Childers, 2009, p.
7), suggesting that re-nesting is unlikely
to offset losses due to predation. Losses
of breeding hens and young chicks to
predation potentially can influence
overall greater and Gunnison sagegrouse population numbers, as these
two groups contribute most significantly
to population productivity (GSRSC,
2005, p. 29, Baxter et al. 2008, p. 185;
Connelly et al, in press a, p. 18).
Nesting success of greater sage-grouse
is positively correlated with the
presence of big sagebrush and grass and
forb cover (Connelly et al. 2000, p. 971).
Females actively select nest sites with
these qualities (Schroeder and Baydack
2001, p. 25; Hagen et al. 2007, p. 46).
Nest predation appears to be related to
the amount of herbaceous cover
surrounding the nest (Gregg et al. 1994,
p. 164; Braun 1995, pp. 1-2; DeLong et
al. 1995, p. 90; Braun 1998; Coggins
1998, p. 30; Connelly et al. 2000b, p.
975; Schroeder and Baydack 2001, p. 25;
Coates and Delehanty 2008, p. 636).
Loss of nesting cover from any source
(e.g., grazing, fire) can reduce nest
success and adult hen survival.
However, Coates (2007, p. 149) found
that badger predation was facilitated by
nest cover as it attracts small mammals,
a badger’s primary prey. Similarly,
habitat alteration that reduces cover for
young chicks can increase their rate of
predation (Schroeder and Baydack 2001,
p. 27).
In a review of published nesting
studies, Connelly et al. (in press, p. 14)
reported that nesting success was
greater in unaltered habitats versus
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habitats affected by anthropogenic
activities. Where greater sage-grouse
habitat has been altered, the influx of
predators can decrease annual
recruitment into a population (Gregg et
al. 1994, p. 164; Braun 1995, pp. 1-2;
Braun 1998; DeLong et al. 1995, p. 91;
Schroeder and Baydack 2001, p. 28;
Coates 2007, p. 2; Hagen in press, p. 7).
Agricultural development, landscape
fragmentation, and human populations
have the potential to increase predation
pressure on all life stages of greater sagegrouse by forcing birds to nest in less
suitable or marginal habitats, increasing
travel time through altered habitats
where they are vulnerable to predation,
and increasing the diversity and density
of predators (Ritchie et al. 1994, p. 125;
Schroeder and Baydack 2001, p. 25;
Connelly et al. 2004, p. 7-23; and
Summers et al. 2004, p. 523). We
believe the aforementioned is also
applicable to Gunnison sage-grouse
because overall behavior and life-history
traits are similar for the two species
(Young 1994, p. 4).
Abundance of red fox and corvids,
which historically were rare in the
sagebrush landscape, has increased in
association with human-altered
landscapes (Sovada et al. 1995, p. 5). In
the Strawberry Valley of Utah, low
survival of greater sage-grouse may have
been due to an unusually high density
of red foxes, which apparently were
attracted to that area by anthropogenic
activities (Bambrough et al. 2000). The
red fox population has increased within
the Gunnison Basin (BLM, 2009, p. 37).
Ranches, farms, and housing
developments have resulted in the
introduction of nonnative predators
including domestic dogs (Canis
domesticus) and cats (Felis domesticus)
into greater sage-grouse habitats
(Connelly et al. 2004, p. 12-2). We
believe this is also applicable to
Gunnison sage-grouse because of the
habitat similarities of the two species
and similar patterns of human
development. Local attraction of ravens
to nesting hens may be facilitated by
loss and fragmentation of native
shrublands, which increases exposure of
nests to potential predators (Aldridge
and Boyce 2007, p. 522; Bui 2009, p.
32). The presence of ravens was
negatively associated with greater sagegrouse nest and brood fate in western
Wyoming (Bui 2009, p. 27).
Raven abundance has increased as
much as 1,500 percent in some areas of
western North America since the 1960s
(Coates 2007, p. 5). Breeding bird survey
trends from 1966 to 2007 indicate
increases throughout Colorado and Utah
(USGS, 2009, pp. 1-2). Increases in
raven numbers are suggested in the
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Pınon Mesa population, though data
have not been collected (CDOW 2009a,
p. 110). Human-made structures in the
environment increase the effect of raven
predation, particularly in low canopy
cover areas, by providing ravens with
perches (Braun 1998, pp.145-146;
Coates 2007, p. 155; Bui 2009, p. 2).
Reduction in patch size and diversity of
sagebrush habitat, as well as the
construction of fences, powerlines and
other infrastructure also are likely to
encourage the presence of the common
raven (Coates et al. 2008, p. 426; Bui
2009, p. 4). For example, raven counts
have increased by approximately 200
percent along the Falcon-Gondor
transmission line corridor in Nevada
(Atamian et al. 2007, p. 2). Atamian et
al. (2007, p. 2) found that ravens
contributed to lek disturbance events in
the areas surrounding the transmission
line. However, cause of decline in
surrounding sage-grouse population
numbers could not be separated from
other potential impacts. Holloran (2005,
p. 58) attributed increased sage-grouse
nest depredation to high corvid
abundances, which resulted from
anthropogenic food and perching
subsidies in areas of natural gas
development in western Wyoming. Bui
(2009, p. 31) also found that ravens used
road networks associated with oil fields
in the same Wyoming location for
foraging activities. Holmes (2009, pp. 24) also found that common raven
abundance increased in association with
oil and gas development in
southwestern Wyoming. Raven
abundance was strongly associated with
sage-grouse nest failure in northeastern
Nevada, with resultant negative effects
on sage-grouse reproduction (Coates
2007, p. 130). The presence of high
numbers of predators within a sagegrouse nesting area may negatively
affect sage-grouse productivity without
causing direct mortality. Coates (2007,
pp. 85-86) suggested that ravens may
reduce the time spent off the nest by
female sage-grouse, thereby potentially
compromising their ability to secure
sufficient nutrition to complete the
incubation period.
As more suitable grouse habitat is
converted to exurban development,
agriculture, or other non-sagebrush
habitat types, grouse nesting and broodrearing become increasingly spatially
restricted (Bui 2009, p. 32). As
discussed in Factor A, we anticipate a
substantial increase in the distribution
of residential development throughout
the range of Gunnison sage-grouse. This
increase will likely cause additional
restriction of nesting habitat within the
species’ range, given removal of
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sagebrush habitats and the strong
selection for sagebrush by the species.
Additionally, Gunnison sage-grouse
avoid residential development, resulting
in functional habitat loss (Aldridge et al.
2010, p. 24). Ninety-one percent of nest
locations in the western portion of the
Gunnison Basin population occur
within 35 percent of the available
habitat (Aldridge et al. 2010, p. 25-26).
Unnaturally high nest densities which
result from habitat fragmentation or
disturbance associated with the
presence of edges, fencerows, or trails
may increase predation rates by making
foraging easier for predators (Holloran
2005, p. C37). Increased nest density
could negatively influence the
probability of a successful hatch
(Holloran and Anderson, 2005, p. 748).
The influence of the human footprint in
sagebrush ecosystems may be
underestimated (Leu and Hanser, in
press, pp. 24-25) since it is uncertain
how much more habitat sage-grouse (a
large landscape-scale species) need for
persistence in increasingly fragmented
landscapes (Connelly et al., in press, pp.
28-34). Therefore, the influence of
ravens and other predators associated
with human activities may be
underestimated.
Ongoing studies in the San Miguel
population suggest that the lack of
recruitment in Gunnison sage-grouse is
likely due to predation (CDOW 2009a,
p. 31). In this area, 6 of 12 observed
nests were destroyed by predation, with
none of the chicks from the remaining
nests surviving beyond two weeks
(CDOW 2009a, p. 30). In small and
declining populations, small changes to
habitat abundance or quality, or in
predator abundance, could have large
consequences.
Predator removal efforts have
sometimes shown short-term gains that
may benefit fall populations, but not
breeding population sizes (Cote and
Sutherland 1997, p. 402; Hagen in press,
p. 9; Leu and Hanser in press, p. 27).
Predator removal may have greater
benefits in areas with low habitat
quality, but predator numbers quickly
rebound without continual control
(Hagen in press, p. 9). Red fox removal
in Utah appeared to increase adult
greater sage-grouse survival and
productivity, but the study did not
compare these rates against other nonremoval areas, so inferences are limited
(Hagen in press, p. 11).
Slater (2003, p. 133) demonstrated
that coyote control failed to have an
effect on greater sage-grouse nesting
success in southwestern Wyoming.
However, coyotes may not be an
important predator of sage-grouse. In a
coyote prey base analysis, Johnson and
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Hansen (1979, p. 954) showed that sagegrouse and bird egg shells made up a
very small percentage (0.4–2.4 percent)
of analyzed scat samples. Additionally,
coyote removal can have unintended
consequences resulting in the release of
smaller predators, many of which, like
the red fox, may have greater negative
impacts on sage-grouse (Mezquida et al.
2006, p. 752).
Removal of ravens from an area in
northeastern Nevada caused only shortterm reductions in raven populations
(less than one year), as apparently
transient birds from neighboring sites
repopulated the removal area (Coates
2007, p. 151). Additionally, badger
predation appeared to partially
compensate for decreases due to raven
removal (Coates 2007, p. 152). In their
review of literature regarding predation,
Connelly et al. (2004, p. 10-1) noted that
only two of nine studies examining
survival and nest success indicated that
predation had limited a sage-grouse
population by decreasing nest success,
and both studies indicated low nest
success due to predation was ultimately
related to poor nesting habitat. Bui
(2009, pp. 36-37) suggested removal of
anthropogenic subsidies (e.g., landfills,
tall structures) may be an important step
to reducing the presence of sage-grouse
predators. Leu and Hanser (in press, p.
27) also argue that reducing the effects
of predation on sage-grouse can only be
effectively addressed by precluding
these features.
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Summary of Predation
Predation has a strong relationship
with anthropogenic factors on the
landscape, and human presence on the
landscape will continue to increase for
the foreseeable future.
Gunnison sage-grouse are adapted to
minimize predation by cryptic plumage
and behavior. Gunnison sage-grouse
may be increasingly subject to levels of
predation that would not normally
occur in the historically contiguous
unaltered sagebrush habitats. The
impacts of predation on greater sagegrouse can increase where habitat
quality has been compromised by
anthropogenic activities (exurban
development, road development, etc.)
(e.g., Coates 2007, p. 154, 155; Bui 2009,
p. 16; Hagen in press, p. 12). Landscape
fragmentation, habitat degradation, and
human populations have the potential
to increase predator populations
through increasing ease of securing prey
and subsidizing food sources and nest
or den substrate. Thus, otherwise
suitable habitat may change into a
habitat sink for grouse populations
(Aldridge and Boyce 2007, p. 517).
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Anthropogenic influences on
sagebrush habitats that increase
suitability for ravens may also limit
sage-grouse populations (Bui 2009, p.
32). Current land-use practices in the
intermountain West favor high predator
(in particular, raven) abundance relative
to historical numbers (Coates et al.
2008, p. 426). The interaction between
changes in habitat and predation may
have substantial effects to the Gunnison
sage-grouse at the landscape level
(Coates 2007, p. 3-5). Since the
Gunnison and greater sage-grouse have
such similar behavior and life-history
traits, we believe the current impacts on
Gunnison sage-grouse are at least as
significant as those documented in
greater sage-grouse and to date in
Gunnison sage-grouse. Given the small
population sizes and fragmented nature
of the remaining Gunnison sage-grouse
habitat, we believe that the impacts of
predation will likely be even greater as
habitat fragmentation continues.
The studies presented above for
greater sage-grouse suggest that, in areas
of intensive habitat alteration and
fragmentation, sage-grouse productivity
and, therefore, populations could be
negatively affected by increasing
predation. Nest predation may be
higher, more variable, and have a greater
impact on the small, fragmented
Gunnison sage-grouse populations,
particularly the six smallest populations
(GSRSC 2005, p. 134). Unfortunately,
except for the relatively few studies
presented here, data are lacking that
link Gunnison sage-grouse population
numbers and predator abundance.
However, in at least six of the seven
populations (Gunnison Basin
potentially excluded), where habitats
have been significantly altered by
human activities, we believe that
predation could be limiting Gunnison
sage-grouse populations. As more
habitats face development, even
dispersed development such as that
occurring throughout the range of
Gunnison sage-grouse, we expect this
threat to spread and increase. Studies of
the effectiveness of predator control
have failed to demonstrate a long-term
inverse relationship between the
predator numbers and sage-grouse
nesting success or population numbers.
Therefore, we believe that predation is
currently a threat to the Gunnison sagegrouse and will continue to be a threat
to the species within the foreseeable
future.
Summary of Factor C
We have reviewed the available
information on the effects of disease and
predation on the Gunnison sage-grouse.
The only disease that currently presents
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a potential impact to the Gunnison sagegrouse is West Nile virus. This virus is
distributed throughout most of the
species’ range. However, despite its near
100 percent lethality, disease
occurrence is sporadic in other taxa
across the species’ range and has not
been detected to date in Gunnison sagegrouse. While we have no evidence of
West Nile virus acting on the Gunnison
sage-grouse, because of its presence
within the species’ range and the
continued development of
anthropogenic water sources in the area,
the virus may pose a future threat to the
species. We anticipate that West Nile
virus will persist within the range of
Gunnison sage-grouse indefinitely and
will be exacerbated by any factor (e.g.,
climate change) that increases ambient
temperatures and the presence of the
vector on the landscape.
We believe that existing and
continued landscape fragmentation will
increase the effects of predation on this
species, particularly in the six smaller
populations, resulting in a reduction in
sage-grouse productivity and abundance
in the future.
We have evaluated the best available
scientific information regarding disease
and predation and their effects on the
Gunnison sage-grouse. Based on the
information available, we have
determined that predation is a
significant threat to the species
throughout all or a significant portion of
its range. Furthermore, we determine
that disease is not currently a significant
threat but has the potential to become a
significant threat at any time.
D. The Inadequacy of Existing
Regulatory Mechanisms
Under this factor, we examine
whether threats to the Gunnison sagegrouse are adequately addressed by
existing regulatory mechanisms.
Existing regulatory mechanisms that
could provide some protection for
Gunnison sage-grouse include: (1) local
land use laws, processes, and
ordinances; (2) State laws and
regulations; and (3) Federal laws and
regulations. An example of a regulatory
mechanism is the terms and conditions
attached to a grazing permit that
describe how a permittee will manage
livestock on a BLM allotment. They are
non-discretionary and enforceable, and
are considered a regulatory mechanism
under this analysis. Other examples
include city or county ordinances, State
governmental actions enforced under a
State statute or constitution, or Federal
action under statute. Actions adopted by
local groups, States, or Federal entities
that are discretionary or are not
enforceable, including conservation
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strategies and guidance, are typically
not regulatory mechanisms.
Regulatory mechanisms, if they exist,
may preclude the need for listing if such
mechanisms are judged to adequately
address the threat to the species such
that listing is not warranted. Conversely,
threats on the landscape are exacerbated
when not addressed by existing
regulatory mechanisms, or when the
existing mechanisms are not adequate
(or not adequately implemented or
enforced). We cannot predict when or
how local, State, and Federal laws,
regulations, and policies will change;
however, most Federal land use plans
are valid for at least 20 years. In this
section we review actions undertaken
by local, State, and Federal entities
designed to reduce or remove threats to
Gunnison sage-grouse and its habitat.
Local Laws and Regulations
Rangewide approximately 41 percent
of occupied Gunnison sage-grouse
habitat is privately owned (calculation
from Table 1). Gunnison County and
San Miguel County, Colorado, are the
only local or County entities that have
regulations and policy, respectively,
that provide a level of conservation
consideration for the Gunnison sagegrouse or its habitats on private land
(Dolores County 2002; Mesa County
2003; Montrose County 2003). In 2007,
the Gunnison County, Colorado Board
of County Commissioners approved
Land Use Resolution (LUR) Number 0717 to ensure all applications for land
use change permits, including building
permits, individual sewage disposal
system permits, Gunnison County
access permits, and Gunnison County
Reclamation permits be reviewed for
impact to Gunnison sage-grouse habitat
within 1 km (0.6 mile) of an active lek.
If impacts are determined to result from
a project, impacts are to be avoided,
minimized, and/or mitigated.
Approximately 79 percent of private
land occupied by the Gunnison Basin
population is in Gunnison County, and
thereby under the purview of these
regulations. The remaining 21 percent of
the private lands in the Gunnison Basin
population is in Saguache County where
similar regulations are not in place or
applicable. Actions outside the 1 km
(0.6 mi) buffer are not subject to
Gunnison County LUR 07-17.
Colorado State statute (C.R.S. 30-28101) exempts parcels of land of 14 ha
(35 ac) or more per home from
regulation, so county zoning laws in
Colorado such as LUR 07-17 only apply
to properties with housing densities
greater than one house per 14 ha (35 ac).
This statute allows these parcels to be
exempt from county regulation and may
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negatively affect Gunnison sage-grouse
by allowing for further development,
degradation, and loss of the species’
habitat. A total of 1,190 parcels,
covering 16,351 ha (40,405 ac), within
occupied habitat in Gunnison County
currently contain development. Of those
1,190 parcels, 851 are less than 14 ha
(35 ac) in size and subject to County
review. However, those 851 parcels
encompass only 13.1 percent of private
land area with existing development in
occupied habitat within Gunnison
County. Parcels greater than 14 ha (35
ac) in size (339 of the 1,190) encompass
86.9 of the existing private land area
within occupied habitat within
Gunnison County. Cumulatively, 91
percent of the private land within the
Gunnison County portion of the
Gunnison Basin population that either
has existing development or is
potentially developable land is allocated
in lots greater than 14 ha (35 ac) in size
and therefore not subject to Gunnison
County LUR 07-17. This situation limits
the effectiveness of LUR 07-17 in
providing protection to Gunnison sagegrouse in Gunnison County.
The only required review by
Gunnison County under LUR 07-17
pertains to the construction of roads,
driveways, and individual building
permits. Of the 79 percent of area
occupied by the Gunnison Basin
population that falls within Gunnison
County, 37 percent of the private land
is not subject to the County LUR
because the action would not be within
1 km (0.6 mi) of a lek. Gunnison County
reviewed 231 projects from July 2006
through November 2009 under the LUR
for impacts to Gunnison sage-grouse. All
but one project was within the overall
boundary of the Gunnison Basin
population’s occupied habitat, with
most of the activity focused in the
northern portion of this population. All
of these projects were approved and
allowed to proceed. The majority of
these projects were within established
areas of development, and some were
for activities such as outbuildings or
additions to existing buildings;
nonetheless, these projects provide an
indication of further encroachment and
fragmentation of the remaining
occupied habitat. Nineteen percent (44)
of the projects were within 1 km (0.6
mi) of a lek. Nineteen percent (45) of the
projects contained language within the
permit that established conditions for
control of pets. The use of the 1-km (0.6mi) buffer around the lek provides some
conservation benefit to the grouse. This
buffer is not as large as that
recommended by GSRSC (2005 entire)
to meet all the species’ year-round life-
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history needs (6.4 km (4 mi)). Because
research summarized in GSRSC (2005
entire) has shown that impacts occur up
to 6.4 km (4 mi) from the point of
disturbance, these minimally or
unregulated negative impacts will
continue to fragment the habitat and
thus have substantial impacts on the
local, as well as landscape, conservation
of the species. In summary, Gunnison
County is to be highly commended for
the regulatory steps they have
implemented. However, the scope and
implementation of that regulatory
authority is limited in its ability to
effectively and collectively conserve
Gunnison sage-grouse due to the
County’s limited authority within the
Gunnison Basin portion of the species’
range.
In 2005, San Miguel County amended
its Land Use Codes to include
consideration and implementation, to
the extent possible, of conservation
measures recommended in GSRSC
(2005, entire) for the Gunnison sagegrouse when considering land use
activities and development located
within its habitat (San Miguel County
2005). The County is only involved
when there is a request for a special use
permit, which limits their involvement
in review of projects adversely affecting
Gunnison sage-grouse and their habitat
and providing recommendations.
Conservation measures are solicited
from the CDOW and a local Gunnison
sage-grouse working group.
Implementation of the conservation
measure is dependent on negotiations
between the County and the applicant.
Some positive measures (e.g., locating a
special use activity outside grouse
habitat, establishing a 324-ha (800-ac)
conservation easement; implementing
speed limits to reduce likelihood of
bird/vehicle collisions) have been
implemented as a result of the policy.
Typically, the County has not been
involved with residential development,
and most measures that result from
discussions with applicants result in
measures that the Service considers
minimization, not mitigation measures,
but which the County considers
mitigation (Henderson 2010, pers.
comm.). The San Miguel County Land
Use Codes provide some conservation
benefit to the species through some
minimization of impacts and
encouraging landowners to voluntarily
minimize/mitigate impacts of
residential development in grouse
habitat. However, the codes allow for
limited regulatory authority but are not
sufficient to prevent or mitigate for the
continued degradation and
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fragmentation of Gunnison sage-grouse
habitat.
In addition to the county regulations,
Gunnison County hired a Gunnison
Sage-grouse Coordinator (2005 to
present) and organized a Strategic
Committee (2005 to present) to facilitate
implementation of conservation
measures in the Gunnison Basin under
both the local Conservation Plan and
Rangewide Conservation Plan (RCP)
(GSRSC 2005). San Miguel County hired
a Gunnison Sage-grouse Coordinator for
the San Miguel Basin population in
March 2006. The Crawford working
group hired a Gunnison sage-grouse
coordinator in December 2009.
Saguache County has applied for a grant
to hire a part-time coordinator for the
Poncha Pass population (grant status
still pending). These efforts facilitate
coordination relative to sage-grouse
management and reflect positively on
these Counties’ willingness to conserve
Gunnison sage-grouse, but have no
regulatory authority. None of the other
Counties with Gunnison sage-grouse
populations have regulations, or staff,
that implement regulation or policy
review that consider the conservation
needs of Gunnison sage-grouse. The
inadequacy of existing regulatory
mechanisms that address habitat loss,
fragmentation, and degradation, in the
other populations constitutes a threat to
those populations.
Conservation measures that have
regulatory authority that have been
implemented as a result of the
aforementioned collective efforts
include: closing of shed antler
collection in the Gunnison Basin by the
Colorado Wildlife Commission due to
its disturbance of Gunnison sage-grouse
during the early breeding season; and a
BLM/USFS/Gunnison County/CDOW
collective effort to implement and
enforce road closures during the early
breeding season (March 15 to May 15).
These regulatory efforts have provided
benefits to Gunnison sage-grouse during
the breeding season. However, these
measures do not adequately address the
primary threat to the species of
fragmentation of the habitat.
Habitat loss is not regulated or
monitored in Colorado counties where
Gunnison sage-grouse occur. Therefore,
conversion of agricultural land from one
use to another, such as native pasture
containing sagebrush converted to
another use, such as cropland, would
not normally come before a county
zoning commission. Based on the
information we have available for the
range of the species, we do not believe
that habitat loss from conversion of
sagebrush habitat to agricultural lands is
occurring at a level that makes it a
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threat. The permanent loss, and
associated fragmentation and
degradation, of sagebrush habitat is
considered the largest threat to
Gunnison sage-grouse (GSRSC 2005, p.
2). The minimally regulated residential/
exurban development found throughout
the vast majority of the species range is
a primary cause of this loss,
fragmentation, and degradation of
Gunnison sage-grouse habitat. We are
not aware of any existing local
regulatory mechanisms that adequately
address this threat.
We recognize that county or city
ordinances in San Juan County, Utah,
that address agricultural lands,
transportation, and zoning for various
types of land uses have the potential to
influence sage-grouse. However, we are
not aware of any existing County
regulations that provide adequate
regulatory mechanisms to address
threats to the Gunnison sage-grouse and
its habitat.
Each of the seven populations of
Gunnison sage-grouse has a
Conservation Plan written by the
respective local working group with
publication dates of 1999 to 2009. These
plans provide recommendations for
management of Gunnison sage-grouse
and have been the basis for identifying
and prioritizing local conservation
efforts, but do not provide regulatory
protection for Gunnison sage-grouse or
its habitat.
State Laws and Regulations
State laws and regulations provide
specific authority for sage-grouse
conservation over lands that are directly
owned by the State, provide broad
authority to regulate and protect
wildlife on all lands within their
borders, and provide a mechanism for
indirect conservation through regulation
of threats to the species (e.g., noxious
weeds).
Colorado Revised Statutes, Title 33,
Article 1 gives CDOW responsibility for
the management and conservation of
wildlife resources within State borders.
Title 33 Article 1-101, Legislative
Declaration requires a continuous
operation of planning, acquisition, and
development of wildlife habitats and
facilities for wildlife-related
opportunities. The CDOW is required by
statute (C.R.S. 106-7-104) to provide
counties with information on
‘‘significant wildlife habitat,’’ and
provide technical assistance in
establishing guidelines for designating
and administering such areas, if asked.
The CDOW also has authority to
regulate possession of the Gunnison
sage-grouse, set hunting seasons, and
issue citations for poaching. These
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authorities provide individual Gunnison
sage-grouse with protection from direct
human-caused mortality to the level that
hunting is not considered a threat to the
species (see Factor B discussion, above).
The Colorado Wildlife Commission is
currently considering whether to
include the Gunnison sage-grouse as an
endangered or threatened species in
accordance with Administrative
Directive W-7 (State of Colorado, 2007,
entire). These authorities do not regulate
the primary threat to the species of
fragmentation of habitat as described in
Factor A.
The Wildlife Resources Code of Utah
(Title 23) provides UDWR the powers,
duties, rights, and responsibilities to
protect, propagate, manage, conserve,
and distribute wildlife throughout the
State. Section 23-13-3 declares that
wildlife existing within the State, not
held by private ownership and legally
acquired, is property of the State.
Sections 23-14-18 and 23-14-19
authorize the Utah Wildlife Board to
prescribe rules and regulations for the
taking and/or possession of protected
wildlife, including Gunnison sagegrouse. These authorities provide
adequate protection to individual
Gunnison sage-grouse from direct,
human-caused mortality to the level that
hunting is not considered a threat to the
species (see Factor B discussion, above).
However, these laws and regulations do
not provide the regulatory authority
needed to conserve sage-grouse habitats
from the threats described in Factor A.
Gunnison sage-grouse are managed by
CDOW and UDWR on all lands within
each State as resident native game birds.
In both States this classification allows
the direct human taking of the bird
during hunting seasons authorized and
conducted under State laws and
regulations. In 2000, CDOW closed the
hunting season for Gunnison sagegrouse in the Gunnison Basin, the only
area then open to hunting for the
species. The hunting season for
Gunnison sage-grouse in Utah has been
closed since 1989. The Gunnison sagegrouse is listed as a species of special
concern in Colorado, as a sensitive
species in Utah, and as a Tier I species
under the Utah Wildlife Action Plan,
providing heightened priority for
management (CDOW 2009a, p. 40;
UDWR 2009, p. 9). The Colorado
Wildlife Commission is currently
considering a proposal from CDOW to
list the Gunnison sage-grouse as a State
endangered or threatened species. State
listed species will be the focus of
conservation actions such as
monitoring, research, enhancement,
restoration, or inventory, and will
receive preferential consideration in the
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annual budget development process
(State of Colorado, 2007, p. 1). Hunting
and other State regulations that deal
with issues such as harassment provide
adequate protection for individual birds
(see discussion under Factor B), but do
not protect the habitat. While we
strongly support the use of regulatory
mechanisms to control hunting of the
species, the protection afforded through
the aforementioned State regulatory
mechanisms is limited.
Easements that prevent long-term or
permanent habitat loss by prohibiting
development are held by CDOW,
UDWR, Natural Resources Conservation
Service (NRCS), NPS, and nongovernmental organizations (Table 4).
Although the decision of whether to
enter into a conservation easement is
voluntary on the part of the landowner,
conservation easements are legally
binding documents. Therefore, we have
determined that perpetual conservation
easements offer some level of regulatory
protection to the species. Some of the
easements include conservation
measures that are specific for Gunnison
sage-grouse, while many are directed at
other species, such as big game (GSRSC
2005, pp. 59-103). Some of these
easements protect existing Gunnison
sage-grouse habitat. Sixty-nine percent
of the area under conservation
easements have land cover types other
than agricultural (covering 31 percent)
that provide habitat for Gunnison sagegrouse. However, considering that the
total easements recorded to date cover
only 5.1 percent of private lands
rangewide, that not all easements have
sage-grouse specific habitat or
conservation measures, and their
scattered distribution throughout the
range of the species, we believe that
while easements provide some level of
protection from future development,
they are not sufficient to ameliorate the
threat of loss and fragmentation of
Gunnison sage-grouse habitat. We
believe this to be true now and into the
future, especially considering the costs
of purchasing easements when
compared to the cost paid for
development of those lands, and money
available through all sources to
purchase easements. In addition,
because entering into a conservation
easement is voluntary on the part of the
landowner, we cannot be sure that any
future conservation easements will
occur in such a configuration and
magnitude that they will offer the
species or its habitat substantial
protection.
TABLE 4. AREA OF CONSERVATION EASEMENTS IN HECTARES (HA) AND ACRES (AC) BY POPULATION AND PERCENTAGE OF
OCCUPIED HABITAT IN CONSERVATION EASEMENTS AS OF SEPTEMBER 2009.
Population
hectares
Gunnison Basin
Percent of
Occupied
Habitat in
Respective
Population
acres
11,334
28,008
4.7
˜
Pinon Mesa
4,270
10,551
27.1
Cerro Summit-Cimarron-Sims Mesa
1,395
3,447
9.3
Monticello
1,036
2,560
3.6
San Miguel Basin
843
2,084
2.1
Dove Creek Group
330
815
2.0
Crawford
249
616
1.8
0
0
0
19,457
48,081
5.1
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Rangewide
The CDOW has been implementing
the CCAA referenced earlier in this
document. As of February 2010, 4
landowners have completed Certificates
of Inclusion (CI) for their properties
enrolling 2,581 ha (6,377 ac). Because
the Service issues a permit to applicants
with an approved CCAA, we have some
regulatory oversight over the
implementation of the CCAA. However,
permit holders and landowners can
voluntarily opt out of the CCAA at any
time. Thus, the CCAA provides
important conservation measures that
assist the species, and provides
regulatory protection to enrolled
landowners, but due to its voluntary
nature, provides no regulatory
protection. An additional 38
landowners (totaling approximately
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18,211 ha (45,000 ac) within Gunnison
sage-grouse occupied habitat), have
worked with the CDOW to complete
baseline reports in preparation for
issuance of CIs. The reports describe
property infrastructure and number of
acres of Gunnison sage-grouse seasonal
habitat. A CDOW review of all these
reports and the condition of the habitat
is pending. The CCAA/CI efforts
described in this paragragh will provide
conservation benefits to Gunnison sagegrouse throughout their range where
they are in place (27 in the Gunnison
Basin, 3 in San Miguel, 2 in Crawford,
˜
5 in Pınon Mesa, 1 in Dove Creek). Even
assuming the area of all landowners
expressing interest and with completed
baselines will ultimately be covered
under CIs, the fact remains that these
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properties constitute only 13 percent of
the total private land throughout the
species range and that they are scattered
throughout the species range. Therefore,
we do not believe the CCAA/CI efforts
would provide adequate regulatory
coverage to ensure the long-term
conservation of the species on private
lands.
On April 22, 2009, the Governor of
Colorado signed into law new rules
(House Bill 1298) for the Colorado Oil
and Gas Conservation Commission
(COGCC), which is the entity
responsible for permitting oil and gas
well development in Colorado (COGCC
2009, entire). The rules went into effect
on private lands on April 1, 2009, and
on Federal lands July 1, 2009. The new
rules require that permittees and
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operators determine whether their
proposed development location
overlaps with ‘‘sensitive wildlife
habitat,’’ or is within a restricted surface
occupancy (RSO) area. For Gunnison
sage-grouse, areas within 1 km (0.6 mi)
of an active lek can be designated as
RSOs (CDOW 2009a, p. 27), and surface
area occupancy will be avoided except
in cases of economic or technical
infeasibility (CDOW 2009a, p. 27). Areas
within approximately 6.4 km (4 mi) of
an active lek are considered sensitive
wildlife habitat (CDOW 2009a, p. 27)
and the development proponent is
required to consult with the CDOW to
identify measures to (1) avoid impacts
on wildlife resources, including sagegrouse; (2) minimize the extent and
severity of those impacts that cannot be
avoided; and (3) mitigate those effects
that cannot be avoided or minimized
(COGCC 2009, section 1202.a). The
COGCC will consider CDOW’s
recommendations in the permitting
decision, although the final permitting
and conditioning authority remains
with COGCC. As stated in Section
1202.d of the new rules, consultation
with CDOW is not required under
certain circumstances such as, the
issuance of a variance by the Director of
the COGCC, the existence of a
previously CDOW-approved wildlife
mitigation plan, and others. Other
categories for potential exemptions also
can be found in the new rules (e.g.,
1203.b).
Because the new rules have only been
in place for less than a year and their
implementation is still being discussed,
it remains to be seen what level of
protection will be afforded to Gunnison
sage-grouse. The new rules could
provide for greater consideration of the
conservation needs of the species. It
should be noted that leases that have
already been approved but not drilled
(e.g., COGCC 2009, 1202.d(1)), or
drilling operations that are already on
the landscape, may continue to operate
without further restriction into the
future. We are not aware of any
situations where RSOs have been
effectively applied or where
conservation measures have been
implemented for potential oil and gas
development impacts to Gunnison sagegrouse on private lands underlain with
privately owned minerals, which are
regulated by the appropriate governing
bodies.
Colorado and Utah have laws that
directly address the priorities for use of
State school section lands, which
require that management of these
properties be based on maximizing
financial returns. State school section
lands account for only one percent of
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occupied habitat in Colorado and one
percent in Utah, so impacts may be
considered negligible. We are not aware
of any conservation measures that will
be implemented under regulatory
authority for Gunnison sage-grouse on
State school section lands, other than a
request to withdraw or apply ‘‘no
surface occupancy’’ and conservation
measures from the RCP (GSRSC 2005) to
four sections available for oil and gas
leasing in the San Miguel Basin
population (see Factor A for further
discussion). The State Land Board (SLB)
recently purchased the Miramonte
Meadows property (approximately 809
ha (2,000 ac) next to the Dan Noble State
Wildlife Area (SWA). Roughly 526 ha
(1,300 ac) is considered prime Gunnison
sage-grouse habitat (Garner 2010, pers.
comm.). Discussions with the SLB have
indicated a willingness to implement
habitat improvements (juniper removal)
on the property. They have also
accepted an application to designate the
tract as a ‘‘Stewardship Trust’’ parcel.
The Stewardship Trust program is
capped at 119,383 to 121,406 ha
(295,000 to 300,000 ac), and no more
property can be added until another
tract is removed from the program.
Because of this cap, it is unknown if or
when the designation of the tract as a
Stewardship Trust parcel may occur.
The scattered nature of State school
sections (single sections) across the
landscape and the requirement to
conduct activities to maximize financial
returns minimize the likelihood of
implementation of measures that will
benefit Gunnison sage-grouse. Thus,
mechanisms present on State trust lands
are inadequate to minimize degradation
and fragmentation of habitat and thus
ensure conservation of the species.
Some States require landowners to
control noxious weeds, a potential
habitat threat to sage-grouse (as
discussed in Factor A). The types of
plants considered to be noxious weeds
vary by State. Cheatgrass is listed as a
Class C species in Colorado (Colorado
Department of Agriculture 2010, p. 3).
The Class C designation delegates to
local governments the choice of whether
or not to implement activities for the
control of cheatgrass. Gunnison,
Saguache, and Hinsdale Counties target
cheatgrass with herbicide applications
(GWWC 2009, pp. 2- 3). The CDOW
annually sprays for weeds on SWAs
(CDOW 2009a, p. 106). The State of
Utah does not consider cheatgrass as
noxious within the State (Utah
Department of Agriculture 2010, p. 1)
nor in San Juan County (Utah
Department of Agriculture 2010a, p. 1).
The laws dealing with other noxious
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and invasive weeds may provide some
protection for sage-grouse in local areas
by requiring some control of the
invasive plants, although large-scale
control of the most problematic invasive
plants is not occurring. Rehabilitation
and restoration techniques for sagebrush
habitats are mostly unproven and
experimental (Pyke in press, p. 25).
Regulatory authority has not been
demonstrated to be effective in
addressing the overall impacts of
invasive plants on the degradation and
fragmentation of sagebrush habitat
within the species range.
Federal Laws and Regulations
Gunnison sage-grouse are not covered
or managed under the provisions of the
Migratory Bird Treaty Act (16 U.S.C.
703-712) because they are considered
resident game species. Federal agencies
are responsible for managing 54 percent
of the total Gunnison sage-grouse
habitat. The Federal agencies with the
most sagebrush habitat are BLM, an
agency of the Department of the Interior,
and USFS, an agency of the Department
of Agriculture. The NPS in the
Department of the Interior also has
responsibility for lands that contain
Gunnison sage-grouse habitat.
BLM
About 42 percent of Gunnison sagegrouse occupied habitat is on BLMadministered land (Table 1 details
percent ownership within each
population). The Federal Land Policy
and Management Act of 1976 (FLPMA)
(43 U.S.C. 1701 et seq.) is the primary
Federal law governing most land uses
on BLM-administered lands. Section
102(a)(8) of FLPMA specifically
recognizes wildlife and fish resources as
being among the uses for which these
lands are to be managed. Regulations
pursuant to FLPMA and the Mineral
Leasing Act (30 U.S.C. 181 et seq.) that
address wildlife habitat protection on
BLM-administered land include 43 CFR
3162.3-1 and 43 CFR 3162.5-1; 43 CFR
4120 et seq.; and 43 CFR 4180 et seq.
Gunnison sage-grouse have been
designated as a BLM Sensitive Species
since they were first identified and
described in 2000 (BLM 2009, p. 7). The
management guidance afforded
sensitive species under BLM Manual
6840 – Special Status Species
Management (BLM 2008, entire) states
that ‘‘Bureau sensitive species will be
managed consistent with species and
habitat management objectives in land
use and implementation plans to
promote their conservation and to
minimize the likelihood and need for
listing under the ESA’’ (BLM 2008, p.
05V). BLM Manual 6840 further requires
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that Resource Management Plans
(RMPs) should address sensitive
species, and that implementation
‘‘should consider all site-specific
methods and procedures needed to
bring species and their habitats to the
condition under which management
under the Bureau sensitive species
policies would no longer be necessary’’
(BLM 2008, p. 2A1). As a designated
sensitive species under BLM Manual
6840, sage-grouse conservation must be
addressed in the development and
implementation of RMPs on BLM lands.
RMPs are the basis for all actions and
authorizations involving BLMadministered lands and resources. They
establish allowable resource uses,
resource condition goals and objectives
to be attained, program constraints and
general management practices needed to
attain the goals and objectives, general
implementation sequences, and
intervals and standards for monitoring
and evaluating the plan to determine its
effectiveness and the need for
amendment or revision (43 CFR 1601.05(k)).
The RMPs provide a framework and
programmatic guidance for activity
plans, which are site-specific plans
written to implement decisions made in
a RMP. Examples include Allotment
Management Plans that address
livestock grazing, oil and gas field
development, travel management
(motorized and mechanized road and
trail use), and wildlife habitat
management. Activity plan decisions
normally require additional planning
and National Environmental Policy Act
(NEPA) analysis. If an RMP contains
specific direction regarding sage-grouse
habitat, conservation, or management, it
represents an enforceable regulatory
mechanism to ensure that the species
and its habitats are considered during
permitting and other decision-making
on BLM lands.
The BLM manages Gunnison sagegrouse habitat under five existing RMPs.
These RMPs contain some specific
measures or direction pertinent to
management of Gunnison sage-grouse or
their habitats. Three of these RMPs (San
Juan, Grand Junction, and
Uncompahgre– covering all or portions
˜
of the San Miguel, Pınon Mesa,
Crawford, and Cerro Summit–
Cimarron–Sims Mesa populations, and
the Dove Creek group) are in various
stages of revision. All RMPs currently
propose some conservation measures
(measures that if implemented should
provide a level of benefit to Gunnison
sage-grouse) outlined in GSRSC (2005,
entire) or local Gunnison sage-grouse
Conservation Plans through project- or
activity-level NEPA reviews (BLM 2009,
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p. 6). In addition, several offices have
undergone other program-level
planning, such as travel management,
that incorporate some conservation
measures to benefit the species (BLM
2009, p. 6). However, the information
provided to us by the BLM in Colorado
did not specify what requirements,
direction, measures, or guidance will
ultimately be included in the revised
Colorado RMPs to address threats to
sage-grouse and sagebrush habitat.
Additionally we do not know the
effectiveness of these proposed
measures.
We do not have information on RMP
implementation by Utah BLM.
Therefore, we cannot assess the future
value of BLM RMPs as regulatory
mechanisms for the conservation of the
Gunnison sage-grouse. Current BLM
RMPs provide some limited regulatory
authority as they are being implemented
through project-level planning (e.g.,
travel management (the management of
the motorized and nonmotorized use of
public lands) and grazing permit
renewals). We do not know the final
measures that will be included in the
revised RMPs and therefore what will be
implemented, so we cannot evaluate
their effectiveness. Based on modeling
results demonstrating the effects of
roads on Gunnison sage-grouse
(Aldridge and Saher 2010 entire –
discussed in detail in Factor A), we
believe that implementation of even the
most restrictive travel management
alternatives proposed by the BLM and
USFS will still result in further
degradation and fragmentation of
Gunnison sage-grouse habitat in the
Gunnison Basin.
In addition to land use planning, BLM
uses Instruction Memoranda (IM) to
provide instruction to district and field
offices regarding specific resource
issues. Instruction Memoranda are
guidance that require a process to be
followed but do not mandate results.
Additionally, IMs are of short duration
(1 to 2 years) and are intended to
address resource concerns by providing
direction to staff until a threat passes or
the resource issue can be addressed in
a long-term planning document. BLM
issued IM Number CO-2005-038 on July
12, 2005, stating BLM’s intent and
commitment to assist with and
participate in the implementation of the
RCP. Although this IM has not been
formally updated or reissued, it
continues to be used for BLMadministered lands in the State (BLM
2009, p. 6).
The BLM has regulatory authority for
oil and gas leasing on Federal lands and
on private lands with a severed Federal
mineral estate, as provided at 43 CFR
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59841
3100 et seq., and they are authorized to
require stipulations as a condition of
issuing a lease. The BLM’s planning
handbook has program-specific
guidance for fluid minerals (which
include oil and gas) that specifies that
RMP decisions will identify restrictions
on areas subject to leasing, including
closures, as well as lease stipulations
(BLM 2000, Appendix C, p.16). The
handbook also specifies that all
stipulations must have waiver,
exception, or modification criteria
documented in the plan, and notes that
the least restrictive constraint to meet
the resource protection objective should
be used (BLM 2000, Appendix C, p. 16).
The BLM has regulatory authority to
condition ‘‘Application for Permit to
Drill’’ authorizations, conducted under a
lease that does not contain specific sagegrouse conservation stipulations, but
utilization of conditions is discretionary
and we are uncertain as to how this
authority will be applied. Also, oil and
gas leases have a 200-m (650-ft)
stipulation, which allows movement of
the drilling area by that distance to
avoid sensitive resources. Many of the
BLM field offices work with the
operators to move a proposed drilling
site farther or justify such a move
through the site-specific NEPA process.
For existing oil and gas leases on BLM
land in occupied Gunnison sage-grouse
habitat, oil and gas companies can
conduct drilling operations if they wish,
but are always subject to permit
conditions. The BLM has stopped
issuing new drilling leases in occupied
sage-grouse habitat in Colorado at least
until the new RMPs are in place. All
occupied habitat in the Crawford Area
and Gunnison Basin populations are
covered by this policy. However, leases
˜
already exist in 17 percent of the Pınon
Mesa population, and 49 percent of the
San Miguel Basin population. Given the
already small and fragmented nature of
the populations where oil and gas leases
are likely to occur, additional
development within occupied habitat
would negatively impact those
populations by causing additional
actual and functional habitat loss and
fragmentation. Since we do not know
what minimization and mitigation
measures might be applied, we cannot
assess the overall conservation impacts
to those populations.
The oil and gas leasing regulations
authorize BLM to modify or waive lease
terms and stipulations if the authorized
officer determines that the factors
leading to inclusion of the term or
stipulation have changed sufficiently to
no longer justify protection, or if
proposed operations would not cause
unacceptable impacts (43 CFR 3101.1-
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4). The Service has no information
indicating that the BLM has granted any
waivers of stipulations pertaining to the
Gunnison sage-grouse and their habitat.
The Energy Policy and Conservation
Act of 2000 included provisions
requiring the Secretary of the
Department of the Interior to conduct a
scientific inventory of all onshore
Federal lands to identify oil and gas
resources underlying these lands and
the nature and extent of any restrictions
or impediments to the development of
such resources (U.S.C. Title 42, Chapter
77, §6217(a)). On May 18, 2001,
President Bush signed Executive Order
13212-Actions to Expedite EnergyRelated Projects (66 FR 28357, May 22,
2001), which states that the executive
departments and agencies shall take
appropriate actions, to the extent
consistent with applicable law, to
expedite projects that will increase the
production, transmission, or
conservation of energy. The Executive
Order specifies that this includes
expediting review of permits or taking
other actions as necessary to accelerate
the completion of projects, while
maintaining safety, public health, and
environmental protections. Due to the
relatively small amount of energy
development activities occurring within
Gunnison sage-grouse habitat (with the
exception of the Dry Creek Basin
subpopulation of the San Miguel
population), we believe that energy
development activities are not a
significant threat. However, given
scenarios such as Dry Creek Basin, if the
level of energy development activities
should increase, current regulations and
policies do not provide adequate
regulatory protection to prevent oil and
gas development from becoming a threat
to this subpopulation.
As stated previously, Gunnison sagegrouse are considered a BLM Sensitive
Species and therefore receive Special
Status Species management
considerations. The BLM regulatory
authority for grazing management is
provided at 43 CFR 4100 (Regulations
on Grazing Administration Exclusive of
Alaska). Livestock grazing permits and
leases contain terms and conditions
determined by BLM to be appropriate to
achieve management and resource
condition objectives on the public lands
and other lands administered by BLM,
and to ensure that habitats are, or are
making significant progress toward
being, restored or maintained for BLM
special status species (43 CFR
4180.1(d)). The State or regional
standards for grazing administration
must address habitat for endangered,
threatened, proposed, candidate, or
special status species, and habitat
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quality for native plant and animal
populations and communities (43 CFR
4180.2(d)(4) and (5)). The guidelines
must address restoring, maintaining, or
enhancing habitats of BLM special
status species to promote their
conservation, as well as maintaining or
promoting the physical and biological
conditions to sustain native populations
and communities (43 CFR 4180.2(e)(9)
and (10). The BLM is required to take
appropriate action not later than the
start of the next grazing year upon
determining that existing grazing
practices or levels of grazing use are
significant factors in failing to achieve
the standards and conform with the
guidelines (43 CFR 4180.2(c)).
The BLM agreed to work with their
resource advisory councils to expand
the rangeland health standards required
under 43 CFR 4180 so that there are
public land health standards relevant to
all ecosystems, not just rangelands, and
that they apply to all BLM actions, not
just livestock grazing (BLM Manual
180.06.A). Both Colorado and Utah have
resource advisory councils. Within the
Gunnison Basin population, 16 percent
of the BLM and USFS allotment
management plans in occupied habitat
currently have incorporated Gunnison
sage-grouse habitat objectives (USFWS,
2010c, entire). Rangewide, of the offices
providing information specific to
allotment management plans, only 24
percent of 148 BLM and USFS grazing
allotments have thus far incorporated
Gunnison sage-grouse habitat objectives
into the allotment management plans or
in permit renewals. Land health
objectives were being met in 37 of the
80 (46 percent) BLM active allotments
for which data were reported. Land
Health Assessments (LHAs) were not
conducted in an additional 20
allotments.
The BLM Gunnison Field Office
conducted Gunnison sage-grouse habitat
assessments in two major occupied
habitat locations in the Gunnison Basin
population quantifying vegetation
structural characteristics and plant
species diversity. Data were collected
and compared to Gunnison sage-grouse
Structural Habitat Guidelines (GSRSC,
2005, Appendix H) during optimal
growing conditions in these two major
occupied areas. Guidelines for sage
cover, grass cover, forb cover, sagebrush
height, grass height, and forb height
were met in 45, 30, 25, 75, 81, and 39
percent, respectively, of 97 transects
(BLM 2009, pp. 31-32). Using the results
of the two assessments along with
results from LHAs, habitat conditions
are not being adequately managed to
meet the life history requirements of
Gunnison sage-grouse in the majority of
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the Gunnison Basin. Only 40 percent of
the allotments in the San Miguel
population were meeting LHA
objectives. This data suggests that
regulatory mechanisms applied within
livestock grazing permits and leases are
not being implemented such that they
ensure that habitats within two of the
largest Gunnison sage-grouse
populations are making significant
progress toward being restored or
maintained for Gunnison sage-grouse.
USFS
The USFS manages 10 percent of the
occupied Gunnison sage-grouse habitat
(Table 1). Management of National
Forest System lands is guided
principally by the National Forest
Management Act (NFMA) (16 U.S.C.
1600-1614, August 17, 1974, as
amended). The NFMA specifies that all
National Forests must have a Land and
Resource Management Plan (LRMP) (16
U.S.C. 1600) to guide and set standards
for all natural resource management
activities on each National Forest or
National Grassland. The NFMA requires
USFS to incorporate standards and
guidelines into LRMPs (16 U.S.C. 1600).
USFS conducts NEPA analysis on its
LRMPs, which include provisions to
manage plant and animal communities
for diversity, based on the suitability
and capability of the specific land area
in order to meet overall multiple-use
objectives. The USFS planning process
is similar to that of BLM.
The Gunnison sage-grouse is a USFS
sensitive species in both Region 2
(Colorado) and Region 4 (Utah). USFS
policy provides direction to analyze
potential impacts of proposed
management activities to sensitive
species in a biological evaluation. The
forests within the range of sage-grouse
provide important seasonal habitats for
the species, particularly the Grand
Mesa, Uncompahgre, and Gunnison
(GMUG) National Forests. The 1991
Amended Land and Resource
Management Plan for the GMUG
National Forests has not directly
incorporated Gunnison sage-grouse
conservation measures or habitat
objectives. The Regional Forester signed
the RCP and as such has agreed to
follow and implement those
recommendations. Three of the 34
grazing allotments in occupied grouse
habitat have incorporated Gunnison
sage-grouse habitat objectives. To date
USFS has not deferred or withdrawn oil
and gas leasing in occupied habitat, but
sage-grouse conservation measures can
be included at the ‘‘Application for
Permit to Drill’’ stage. The BLM, which
regulates oil and gas leases on USFS
lands, has the authority to defer leases.
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However, the only population within
USFS lands that is in areas of high or
even medium potential for oil and gas
reserves is the San Miguel Basin, and
USFS lands only make up 1.4 percent of
that population (GSRSC 2005, D-8).
While consideration as a sensitive
species and following the
recommendations contained in the
Gunnison sage-grouse Rangewide
Conservation Plan (GSRSC 2005, entire)
can provide some conservation benefits,
they are voluntary in nature.
Considering the aforementioned, the
USFS has minimal regulatory authority
that has been implemented to provide
for the long-term conservation of
Gunnison sage-grouse and its habitat.
NPS
The NPS manages two percent of
occupied Gunnison sage-grouse habitat
(Table 1), which means that there is
little opportunity for the agency to affect
range-wide conservation of the species.
The NPS Organic Act (39 Stat. 535; 16
U.S.C. 1, 2, 3, and 4) states that NPS will
administer areas under their jurisdiction
‘‘by such means and measures as
conform to the fundamental purpose of
said parks, monuments, and
reservations, which purpose is to
conserve the scenery and the natural
and historical objects and the wild life
therein and to provide for the enjoyment
of the same in such manner and by such
means as will leave them unimpaired
for the enjoyment of future generations.’’
Lands in the Black Canyon of the
Gunnison National Park and the
Curecanti National Recreation Area
include portions of occupied habitat of
the Crawford and Gunnison Basin
populations. The 1993 Black Canyon of
the Gunnison Resource Management
Plan (NPS 1993, entire) and the 1995
Curecanti National Recreation Area
Resource Management Plan (NPS 1995,
entire) do not identify any specific
conservation measures for Gunnison
sage-grouse. However, these Resource
Management Plans are outdated and
will be replaced with Resource
Stewardship Strategies, which will be
developed in the next five to seven
years. In the mean time, NPS ability to
actively manage for species of special
concern is not limited by the scope of
their management plans.
NPS completed a Fire Management
Plan in 2006 (NPS 2006, entire). Both
prescribed fire and fire use (allowing
wildfires to burn) are identified as a
suitable use in Gunnison sage-grouse
habitat. However, Gunnison sage-grouse
habitat is identified as a Category C area,
meaning that while fire is a desirable
component of the ecosystem, ecological
constraints must be observed. For
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Gunnison sage-grouse, constraints
include limitation of acreage burned per
year and limitation of percent of project
polygons burned. The NPS is currently
following conservation measures in the
local conservation plans and the RCP
(Stahlnecker 2010, pers. comm.).
In most cases, implementation of NPS
fire management policies should result
in minimal adverse effects since
emphasis is placed on activities that
will minimize, or ideally benefit,
impacts to Gunnison sage-grouse
habitat. Overall, implementation of NPS
regulations should minimize impacts to
Gunnison sage-grouse. Certain activities,
such as human recreation activities
occurring within occupied habitat, may
have adverse effects, although we
believe the limited nature of such
activities on NPS lands would limit
their impacts on the species and thus
not be considered a threat to Gunnison
sage-grouse. Grazing management
activities on NPS lands are governed by
BLM regulations and their
implementation.
Summary of Factor D
Gunnison sage-grouse conservation
has been addressed in some local, State,
and Federal plans, laws, regulations,
and policies. Gunnison County has
implemented regulatory authority over
development within their area of
jurisdiction, for which they are to be
highly commended. No other counties
within the range of the species have
implemented such regulations. While
regulations implemented in Gunnison
County have minimized some impacts,
it has not curtailed the habitat loss,
fragmentation, and degradation
occurring within the County’s
jurisidictional boundary. Due to the
limited scope and applicability of these
regulations throughout the range of the
species and within all populations, the
current local land use or development
planning regulations do not provide
adequate regulatory authority to protect
sage-grouse from development or other
harmful land uses that result in habitat
loss, degradation, and fragmentation.
The CDOW and UDWR have
implemented and continue to pursue
conservation easements in Colorado and
Utah, respectively, to conserve
Gunnison sage-grouse habitat and meet
the species’ needs. These easements
provide protection for the species where
they occur, but do not cover enough of
the landscape to provide for long-term
conservation of the species. State
wildlife regulations provide protection
for individual Gunnison sage-grouse
from direct mortality due to hunting but
do not protect its habitat from the main
threat of loss and fragmentation. Our
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assessment of the implementation of
regulations and associated stipulations
guiding exurban development indicates
that current regulatory measures do not
adequately ameliorate impacts to sagegrouse and its habitat.
Energy development is only
considered a threat in the Dry Creek
Basin subpopulation of the San Miguel
population. For the BLM and USFS,
RMPs and LRMPs are mechanisms
through which adequate and
enforceable protections for Gunnison
sage-grouse could be implemented.
However, the extent to which
appropriate measures to reduce or
eliminate threats to sage-grouse
resulting from the various activites the
agencies manage have been
incorporated into those planning
documents, or are being implemented,
vary across the range. As evidenced by
the discussion above, and the ongoing
threats described under Factor A, BLM
and the USFS are not fully
implementing the regulatory
mechanisms available to conserve
Gunnison sage-grouse and their habitats
on their lands.
We have evaluated the best available
scientific information on the adequacy
of regulatory mechanisms to address
threats to Gunnison sage-grouse and its
habitats. While 54 percent of Gunnison
sage-grouse habitat is managed by
Federal agencies, these lands are
interspersed with private lands, which
do not have adequate regulatory
mechanisms to ameliorate the further
loss and fragmentation of habitat in all
populations. This interspersion of
private lands throughout Federal and
other public lands extends the negative
influence of those activities beyond the
actual 41 percent of occupied habitat
that private lands overlay. While we are
unable to quantify the extent of the
impacts on Federal lands resulting from
activities on private lands, we have
determined that the inadequacy of
regulatory mechanisms on private lands
as they pertain to human infrastructure
development and the inadequate
implementation of Federal authorities
on some Federal lands pose a significant
threat to the species throughout its
range. Further, the threat of inadequate
regulatory mechanisms is expected to
continue or even increase in the future.
E. Other Natural or Manmade Factors
Affecting Its Continued Existence
Other factors potentially affecting the
Gunnison sage-grouse’s continued
existence include genetic risks, drought,
recreational activities, pesticides and
herbicides, and contaminants.
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Genetics and Small Population Size
Small populations face three primary
genetic risks: inbreeding depression;
loss of genetic variation; and
accumulation of new mutations.
Inbreeding can have individual and
population consequences by either
increasing the phenotypic expression of
recessive, deleterious alleles (the
expression of harmful genes through the
physical appearance) or by reducing the
overall fitness of individuals in the
population (GSRSC 2005, p.109 and
references therein). At the species level,
Gunnison sage-grouse have low levels of
genetic diversity particularly when
compared to greater sage-grouse (OylerMcCance et al. 2005, p. 635). There is
no consensus regarding how large a
population must be in order to prevent
inbreeding depression. However, the
San Miguel Basin Gunnison sage-grouse
effective population size was below the
level at which inbreeding depression
has been observed to occur (Stiver et al.
2008, p. 479). Lowered hatching success
is a well documented correlate of
inbreeding in wild bird populations
(Stiver et al. 2008, p. 479 and references
therein). Stiver et al. (2008, p. 479)
suggested the observed lowered
hatching success rate of Gunnison sagegrouse in their study may be caused by
inbreeding depression. Similarities of
hatchability rates exist among other bird
species that had undergone genetic
bottlenecks. The application of the same
procedures of effective population size
estimation as used for the San Miguel
Basin to the other Gunnison sage-grouse
populations indicated that all
populations other than the Gunnison
Basin population may have population
sizes low enough to induce inbreeding
depression; and all populations could
be losing adaptive potential (Stiver et al.
2008, p. 479).
Population structure of Gunnison
sage-grouse was investigated using
mitochondrial DNA sequence (mtDNA,
maternally inherited DNA located in
cellular organelles called mitochondria)
and nuclear microsatellite data from
seven geographic areas (Cerro Summit–
Cimarron–Sims Mesa, Crawford,
Gunnison Basin, Curecanti area of the
Gunnison Basin, Monticello–Dove
˜
Creek, Pınon Mesa, and San Miguel
Basin) (Oyler-McCance et al. 2005,
entire). The Cerro Summit–Cimarron–
Sims Mesa population was not included
in the analysis due to inadequate
sample sizes. The Poncha Pass
population also was not included as it
is composed of individuals transplanted
from Gunnison Basin. Oyler-McCance et
al. (2005, entire) found that levels of
genetic diversity were highest in the
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Gunnison Basin, which consistently had
more alleles and most of the alleles
present in other populations. All other
populations had much lower levels of
diversity.
The lower diversity levels are linked
to small population sizes and a high
degree of geographic isolation.
Collectively, the smaller populations
contain 24 percent of the genetic
diversity of the species. Individually,
each of the small populations may not
be important genetically to the survival
of the species, but collectively it is
likely that 24 percent of the genetic
diversity is important to future
rangewide survival of the species. Some
of the genetic makeup contained within
the smaller populations (with the
potential exception of the Poncha Pass
population since it consists of birds
from the Gunnison Basin) may be
critical to maintaining adaptability in
the face of issues such as climate change
or other environmental change. All
populations sampled were found to be
genetically discrete units (OylerMcCance et al. 2005, p. 635), so the loss
of any of them would result in a
decrease in genetic diversity of the
species. In addition, multiple
populations across a broad geographic
area provide insurance against a single
catastrophic event (such as the effects of
a significant drought even), and the
aggregate number of individuals across
all populations increases the probability
of demographic persistence and
preservation of overall genetic diversity
by providing an important genetic
reservoir (GSRSC 2005, p. 179).
Consequently, the loss of any one
population would have a negative effect
on the species as a whole.
Historically, the Monticello–Dove
˜
Creek, San Miguel, Crawford, and Pınon
Mesa populations were larger and were
connected through more contiguous
areas of sagebrush habitat. A 20 percent
loss of habitat and 37 percent
fragmentation of sagebrush habitat was
documented in southwestern Colorado
between the late 1950s and the early
1990s (Oyler-McCance et al. 2001, p.),
which led to the current isolation of
these populations and is consistent with
the documented low amounts of gene
flow and isolation by distance (OylerMcCance et al. 2005, p. 635). However,
Oyler-McCance et al. (2005, p. 636)
noted that a few individuals in their
analysis appeared to have the genetic
characteristics of a population other
than their own, suggesting they were
dispersers from a different population.
Two probable dispersers were
individuals moving from San Miguel
into Monticello–Dove Creek and
Crawford. The San Miguel population
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itself appeared to have a mixture of
individuals with differing probabilities
of belonging to different clusters. This
information suggests that the San
Miguel population may act as a conduit
of gene flow among the satellite
populations surrounding the larger
Gunnison Basin population.
Additionally, another potential
disperser into Crawford was found from
the Gunnison Basin (Oyler-McCance et
al. 2005, p. 636). This result is not
surprising given their close geographic
proximity.
Effective population size (Ne) is an
important parameter in conservation
biology. It is defined as the size of an
idealized population of breeding adults
that would experience the same rate of
(1) loss of heterozygosity (the amount
and number of different genes within
individuals in a population), (2) change
in the average inbreeding coefficient (a
calculation of the amount of breeding by
closely related individuals), or (3)
change in variance in allele (one
member if a pair or series of genes
occupying a specific position in a
specific chromosome) frequency
through genetic drift (the fluctuation in
gene frequency occurring in an isolated
population) as the actual population.
The effective size of a population is
often much less than its actual size or
number of individuals. As effective
population size decreases, the rate of
loss of allelic diversity via genetic drift
increases. Two consequences of this loss
of genetic diversity, reduced fitness
through inbreeding depression and
reduced response to sustained
directional selection (‘‘adaptive
potential’’), are thought to elevate
extinction risk (Stiver et al., 2008, p. 472
and references therein). While no
consensus exists on the population size
needed to retain a level of genetic
diversity that maximizes evolutionary
potential (i.e., the ability to adapt to
local changes), up to 5,000 greater sagegrouse may be necessary to maintain an
effective population size of 500 birds
(Aldridge and Brigham, 2003, p. 30).
Other recent recommendations also
suggest populations of at least 5,000
individuals to deal with evolutionary
and demographic constraints (Trail et
al. 2009, in press, p. 3, and references
therein). While the persistence of wild
populations is usually influenced more
by ecological rather than by genetic
effects, once they are reduced in size,
genetic factors become increasingly
important (Lande 1995, p. 318).
The CDOW contracted for a
population viability analysis (PVA) for
the Gunnison sage-grouse (GSRSC 2005,
Appendix G). The purpose of the
Gunnison sage-grouse PVA was to assist
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the CDOW in evaluating the relative risk
of extinction for each population under
the conditions at that time (i.e., the risk
of extinction if nothing changed), to
estimate relative extinction probabilities
and loss of genetic diversity over time
for various population sizes, and to
determine the sensitivity of Gunnison
sage-grouse population growth rates to
various demographic parameters
(GSRSC 2005, p. 169). The PVA was
used as a tool to predict the relative, not
absolute or precise, probability of
extinction for the different populations
under various management scenarios
based on information available at that
time and with the understanding that no
data were available to determine how
demographic rates would be affected by
habitat loss or fragmentation. The
analysis indicated that small
populations (< 50 birds) are at a serious
risk of extinction within the next 50
years (assuming some degree of
consistency of environmental influences
in sage-grouse demography). In contrast,
populations in excess of 500 birds had
an extinction risk of less than 5 percent
within the same time period. These
results suggested that the Gunnison
Basin population is likely to persist long
term in the absence of threats acting on
it. In the absence of intervention, the
Cerro Summit–Cimarron–Sims Mesa
and Poncha Pass populations and the
Dove Creek group of the Monticello–
Dove Creek population were likely to
become extirpated (GSRSC 2005, pp.
168-179). Based on 2009 population
estimates and an overall declining
population trend, the same three
populations may soon be extirpated.
Additionally, Gunnison sage-grouse
˜
estimates in the Crawford and Pınon
Mesa populations have declined by over
50 percent since the PVA was
conducted (Table 2), so they too are
likely trending towards extirpation. The
San Miguel population has declined by
40 percent since 2004, so cumulative
factors may be combining to cause its
future extirpation also.
The lack of large expanses of
sagebrush habitat required by Gunnison
sage-grouse in at least six of the seven
Gunnison sage-grouse populations (as
discussed in Factor A), combined with
the results of the PVA and current
population trends suggest that at least
five, and most likely six, of the seven
Gunnison sage-grouse populations are at
high risk of extirpation. The loss of
genetic diversity from the extirpation of
the aforementioned populations would
result in a loss of genetic diversity of the
species as a whole and thus contribute
to decreased functionality of these
remaining populations in maintaining
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viability and adaptability, as well as the
contribution of these populations to
connectivity and the continued
existence of the entire species.
Six of the seven Gunnison sage-grouse
populations may have effective sizes
low enough to induce inbreeding
depression and all seven could be losing
adaptive potential, with the assumption
that the five populations smaller than
the San Miguel population are
exhibiting similar demography to the
San Miguel population (Stiver et al.
2008, p. 479) and thus trending towards
extirpation. Stiver et al. (2008, p. 479)
suggested that long-term persistence of
the six smaller populations would
require translocations to supplement
genetic diversity. The only population
currently providing individuals to be
translocated is the Gunnison Basin
population, but because of substantial
population declines such as those
observed between the 2001 and 2004 lek
counts (Stiver et al., 2008, p. 479),
significant questions arise as to whether
this population would be able to sustain
the loss of individuals required by
translocations. Lek counts, and
consequently population estimates,
especially in the San Miguel Basin and
Gunnison Basin populations, have
undergone substantial declines (Table 2)
since peaks observed in the annual 2004
and 2005 counts, thus making
inbreeding depression even more likely
to be occurring within all populations
except the Gunnison Basin. While we
recognize that sage-grouse population
sizes are cyclical, and that there are
concerns about the statistical reliability
of lek counts and the resulting
population estimates (CDOW 2009a, pp.
1-3), we nonetheless believe that the
overall declining trends of 6 of the 7
Gunnison sage-grouse populations, and
for the species as a whole, are such that
they are having a significant impact on
the species’ ability to persist.
In summary, the declines in estimates
of grouse numbers since 2005 are likely
to contribute to even lower levels of
genetic diversity and higher levels of
inbreeding depression than previously
considered, thus making the species as
a whole less adaptable to environmental
variables and more vulnerable to
extirpation. Based on the information
presented above, we have determined
that genetic risks related to the small
population size of Gunnison sage-grouse
are a threat to the species now and in
the foreseeable future.
Drought
Drought is a common occurrence
throughout the range of the Gunnison
and greater sage-grouse (Braun 1998, p.
148) and is considered a universal
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59845
ecological driver across the Great Plains
(Knopf 1996, p.147). Infrequent, severe
drought may cause local extinctions of
annual forbs and grasses that have
invaded stands of perennial species, and
recolonization of these areas by native
species may be slow (Tilman and El
Haddi 1992, p. 263). Drought reduces
vegetation cover (Milton et al. 1994, p.
75; Connelly et al. 2004, p. 7-18),
potentially resulting in increased soil
erosion and subsequent reduced soil
depths, decreased water infiltration, and
reduced water storage capacity. Drought
also can exacerbate other natural events
such as defoliation of sagebrush by
insects. For example, approximately
2,544 km2 (982 mi2) of sagebrush
shrublands died in Utah in 2003 as a
result of drought and infestations with
the Aroga (webworm) moth (Connelly et
al. 2004, p. 5-11). Sage-grouse are
affected by drought through the loss of
vegetative habitat components, reduced
insect production (Connelly and Braun
1997, p. 9), and potential increased risk
of virus infections, such as the West
Nile virus. These habitat component
losses can result in declining sagegrouse populations due to increased
nest predation and early brood mortality
associated with decreased nest cover
and food availability (Braun 1998, p.
149; Moynahan et al. 2007, p. 1781).
Greater sage-grouse populations
declined during the 1930s period of
drought (Patterson 1952, pp. 68-69;
Braun 1998, p. 148). Drought conditions
in the late 1980s and early 1990s also
coincided with a period when sagegrouse populations were at historically
low levels (Connelly and Braun 1997, p.
8). Although drought has been a
consistent and natural part of the
sagebrush-steppe ecosystem, drought
impacts on sage-grouse can be
exacerbated when combined with other
habitat impacts, such as human
developments, that reduce cover and
food (Braun 1998, p. 148).
Aldridge et al. (2008, p. 992) found
that the number of severe droughts from
1950 to 2003 had a weak negative effect
on patterns of greater sage-grouse
persistence. However, they cautioned
that drought may have a greater
influence on future sage-grouse
populations as temperatures rise over
the next 50 years, and synergistic effects
of other threats affect habitat quality
(Aldridge et al. 2008, p. 992).
Populations on the periphery of the
range may suffer extirpation during a
severe and prolonged drought (Wisdom
et al. in press, p. 22).
Gunnison sage-grouse are capable of
enduring moderate or severe, but
relatively short-term, drought as
observed from persistence of the
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populations during drought conditions
from 1999-2003 throughout much of the
range. The drought that began by at least
2001 and was most severe in 2002 had
varying impacts on Gunnison sagegrouse habitat and is discussed in detail
in our April 18, 2006, finding (71 FR
19954). Habitat appeared to be
negatively affected by drought across a
broad area of the Gunnison sagegrouse’s range. However, the reduction
of sagebrush density in some areas,
allowing for greater herbaceous growth
and stimulating the onset of sagebrush
seed crops may have been beneficial to
sagebrush habitats over the long term.
Six of the seven grouse populations
(except for the Gunnison Basin
population) have decreased in number
since counts were conducted during the
drought year of 2002 (Table 2). Data are
not available to scientifically determine
if the declines are due to the drought
alone. The current status of the various
populations throughout the species’
range make it highly susceptible to
stochastic factors such as drought,
particularly when it is acting in
conjunction with other factors such as
habitat fragmentation, small population
size, predation, and low genetic
diversity. We believe that the available
information is too speculative to
conclude that drought alone is a threat
to the species at this time; however,
based on rapid species decline in
drought years, it is likely that drought
exacerbates other known threats and
thus is an indirect threat to the species.
Recreation
Studies have determined that
nonconsumptive recreational activities
can degrade wildlife resources, water,
and the land by distributing refuse,
disturbing and displacing wildlife,
increasing animal mortality, and
simplifying plant communities (Boyle
and Samson 1985, pp. 110-112). Sagegrouse response to disturbance may be
influenced by the type of activity,
recreationist behavior, predictability of
activity, frequency and magnitude,
timing, and activity location (Knight
and Cole 1995, p. 71). We have not
located any published literature
concerning measured direct effects of
recreational activities on Gunnison or
greater sage-grouse, but can infer
potential impacts on Gunnison sagegrouse from studies on related species
and from research on nonrecreational
activities. Baydack and Hein (1987, p.
537) reported displacement of male
sharp-tailed grouse at leks from human
presence resulting in loss of
reproductive opportunity during the
disturbance period. Female sharp-tailed
grouse were observed at undisturbed
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leks while absent from disturbed leks
during the same time period (Baydack
and Hein 1987, p. 537). Disturbance of
incubating female sage-grouse could
cause displacement from nests,
increased predator risk, or loss of nests.
Disruption of sage-grouse during
vulnerable periods at leks, or during
nesting or early brood rearing could
affect reproduction or survival (Baydack
and Hein 1987, pp. 537-538).
Recreational use of off-highway
vehicles (OHVs) is one of the fastestgrowing outdoor activities. In the
western United States, greater than 27
percent of the human population used
OHVs for recreational activities between
1999 and 2004 (Knick et al., in press, p.
19). Knick et al. (in press, p. 1) reported
that widespread motorized access for
recreation facilitated the spread of
predators adapted to humans and the
spread of invasive plants. Any highfrequency human activity along
established corridors can affect wildlife
through habitat loss and fragmentation
(Knick et al. in press, p. 25). The effects
of OHV use on sagebrush and sagegrouse have not been directly studied
(Knick et al. in press, p. 25). However,
local working groups considered
recreational uses, such as off-road
vehicle use and biking, to be a risk
factor in many areas.
Recreation from OHVs, hikers,
mountain bikes, campers, snowmobiles,
bird watchers, and other sources has
affected many parts of the range,
especially portions of the Gunnison
˜
Basin and Pınon Mesa population (BLM
2005a, p. 14; BLM 2005d, p. 4; BLM
2009, p. 36). These activities can result
in abandonment of lekking activities
and nest sites, energy expenditure
reducing survival, and greater exposure
to predators (GSRSC 2005).
Recreation is a significant use on
lands managed by BLM (Connelly et al.
2004, p. 7-26). Recreational activities
within the Gunnison Basin are
widespread, occur during all seasons of
the year, and have expanded as more
people move to the area or come to
recreate (BLM 2009, pp. 36-37). Four
wheel drive, OHV, motorcycle, and
other means of mechanized travel have
been increasing rapidly. The number of
annual OHV registrations in Colorado
increased from 12,000 in 1991 to
131,000 in 2007 (BLM 2009, p. 37).
Recreational activities are recognized as
a direct and indirect threat to the
Gunnison sage-grouse and their habitat
(BLM 2009, p. 36). The Grand Mesa,
Uncompaghre, and Gunnison (GMUG)
National Forest is the fourth most
visited National Forest in the Rocky
Mountain Region of the USFS (Region 2)
(Kocis et al., 2004 in Draft
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Environmental Impact Statement for
Gunnison Basin Federal Lands Travel
Management (2009, p. 137)). The GMUG
is the second most heavily visited
National Forest on the western slope of
Colorado (DEIS Gunnison Basin Federal
Lands Travel Management 2009, p. 137).
However, it is unknown what
percentage of the visits occur within
Gunnison sage-grouse habitat on the
Gunnison Ranger District ((DEIS
Gunnison Basin Federal Lands Travel
Management 2009, p. 137). With human
populations expected to increase in
towns and cities within and adjacent to
the Gunnison Basin and nearby
populations (see Factor A), we believe
the impacts to Gunnison sage-grouse
from recreational use will continue to
increase.
The BLM and Gunnison County have
38 closure points within the Basin from
March 15 to May 15 each year (BLM
2009, p. 40). While road closures may be
violated in a small number of situations,
we believe that road closures are having
a beneficial effect on Gunnison sagegrouse through avoidance and/or
minimization of impacts during the
breeding season.
Dispersed camping occurs at a low
level on public lands in all of the
populations, particularly during the
hunting seasons for other species.
However, we have no information
indicating that these camping activities
are adversely affecting Gunnison sagegrouse.
Domestic dogs accompanying
recreationists or associated with
residences can disturb, harass, displace,
or kill Gunnison sage-grouse. Authors of
many wildlife disturbance studies
concluded that dogs with people, dogs
on leash, or loose dogs provoked the
most pronounced disturbance reactions
from their study animals (Sime 1999
and references within). The primary
consequences of dogs being off leash is
harassment, which can lead to
physiological stress as well as the
separation of adult and young birds, or
flushing incubating birds from their
nest. However, we have no data
indicating that this activity is adversely
affecting Gunnison sage-grouse
population numbers such that it can be
considered a rangewide or populationlevel threat.
Recreational activities as discussed
above do not singularly pose a
significant threat to Gunnison sagegrouse now or are expected to do so in
the foreseeable future. However, there
may be certain situations where
recreational activities are impacting
local concentrations of Gunnison sagegrouse, especially in areas where habitat
is already fragmented such as in the six
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small populations and in certain areas
within the Gunnison Basin.
Pesticides and Herbicides
Insects are an important component of
sage-grouse chick and juvenile diets
(GSRSC 2005, p.132 and references
therein). Insects, especially ants
(Hymenoptera) and beetles (Coleoptera),
can comprise a major proportion of the
diet of juvenile sage-grouse and are
important components of early broodrearing habitats (GSRSC 2005, p. 132
and references therein). Most pesticide
applications are not directed at control
of ants and beetles. Pesticides are used
primarily to control insects causing
damage to cultivated crops on private
lands and to control grasshoppers
(Orthoptera) and Mormon crickets
(Mormonius sp.) on public lands.
Few studies have examined the effects
of pesticides to sage-grouse, but at least
two have documented direct mortality
of greater sage-grouse from use of these
chemicals. Greater sage-grouse died as a
result of ingestion of alfalfa sprayed
with organophosphorus insecticides
(Blus et al. 1989, p. 1142; Blus and
Connelly 1998, p. 23). In this case, a
field of alfalfa was sprayed with
methamidophos and dimethoate when
approximately 200 greater sage-grouse
were present; 63 of these sage-grouse
were later found dead, presumably as a
result of pesticide exposure (Blus et al.
1989; p. 1142, Blus and Connelly 1998,
p. 23). Both methamidophos and
dimethoate remain registered for use in
the United States (Christiansen and Tate
in press, p. 21), but we found no further
records of sage-grouse mortalities from
their use. In 1950, rangelands treated
with toxaphene and chlordane bait to
control grasshoppers in Wyoming
resulted in game bird mortality of 23.4
percent (Christian and Tate in press, p.
20). Forty-five greater sage-grouse
deaths were recorded, 11 of which were
most likely related to the pesticide
(Christiansen and Tate in press, p. 20,
and references therein). Greater sagegrouse who succumbed to vehicle
collisions and mowing machines in the
same area also were likely compromised
from pesticide ingestion (Christian and
Tate in press, p. 20). Neither of these
chemicals has been registered for
grasshopper control since the early
1980s (Christiansen and Tate in press, p.
20, and references therein).
Infestations of Russian wheat aphids
(Diuraphis noxia) have occurred in
Gunnison sage-grouse occupied range in
Colorado and Utah (GSRSC 2005, p.
132). Disulfoton, a systemic
organophosphate extremely toxic to
wildlife, was routinely applied to over
400,000 ha (million ac) of winter wheat
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crops to control the aphids during the
late 1980s. We have no data indicating
there were any adverse effects to
Gunnison sage-grouse (GSRSC 2005, p.
132). More recently, an infestation of
army cutworms (Euxoa auxiliaries)
occurred in Gunnison sage-grouse
habitat along the Utah-Colorado State
line. Thousands of ha (thousands of ac)
of winter wheat and alfalfa fields were
sprayed with insecticides such as
permethrin by private landowners to
control them (GSRSC 2005, p. 132) but
again, we have no data indicating any
adverse effects to Gunnison sage-grouse.
Game birds that ingested sublethal
levels of pesticides have been observed
exhibiting abnormal behavior that may
lead to a greater risk of predation
(Dahlen and Haugen 1954, p. 477;
McEwen and Brown 1966, p. 609; Blus
et al. 1989, p. 1141). McEwen and
Brown (1966, p. 689) reported that wild
sharp-tailed grouse poisoned by
malathion and dieldrin exhibited
depression, dullness, slowed reactions,
irregular flight, and uncoordinated
walking. Although no research has
explicitly studied the indirect levels of
mortality from sublethal doses of
pesticides (e.g., predation of impaired
birds), it has been assumed to be the
reason for mortality among some study
birds (McEwen and Brown 1966 p. 609;
Blus et al. 1989, p. 1142; Connelly and
Blus 1991, p. 4). Both Post (1951, p. 383)
and Blus et al. (1989, p. 1142) located
depredated sage-grouse carcasses in
areas that had been treated with
insecticides. Exposure to these
insecticides may have predisposed sagegrouse to predation. Sage-grouse
mortalities also were documented in a
study where they were exposed to
strychnine bait used to control small
mammals (Ward et al. 1942 as cited in
Schroeder et al. 1999, p. 16). While we
do not have specific information of
these effects occurring in Gunnison
sage-grouse, we believe the effects
observed in greater sage-grouse can be
expected if similar situations arise
within Gunnison sage-grouse habitat.
Cropland spraying may affect
populations that are not adjacent to
agricultural areas, given the distances
traveled by females with broods from
nesting areas to late brood-rearing areas
(Knick et al. in press, p. 17). The actual
footprint of this effect cannot be
estimated, because the distances sagegrouse travel to get to irrigated and
sprayed fields is unknown (Knick et al.
in press, p. 17). Similarly, actual
mortalities from pesticides may be
underestimated if sage-grouse disperse
from agricultural areas after exposure.
Much of the research related to
pesticides that had either lethal or
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sublethal effects on greater sage-grouse
was conducted on pesticides that have
been banned or have had their use
further restricted for more than 20 years
due to their toxic effects on the
environment (e.g., dieldrin). We
currently do not have any information
to show that the banned pesticides are
having negative impacts to sage-grouse
populations through either illegal use or
residues in the environment. For
example, sage-grouse mortalities were
documented in a study where they were
exposed to strychnine bait used to
control small mammals (Ward et al.
1942 as cited in Schroeder et al. 1999,
p. 16). According to the U.S.
Environmental Protection Agency
(EPA), above-ground uses of strychnine
were prohibited in 1988 and those uses
remain temporarily cancelled today. We
do not know when, or if, above-ground
uses will be permitted to resume.
Currently, strychnine is registered for
use only below-ground as a bait
application to control pocket gophers
(Thomomys sp.; EPA 1996, p. 4).
Therefore, the current legal use of
strychnine baits is unlikely to present a
significant exposure risk to sage-grouse.
No information on illegal use, if it
occurs, is available. We have no other
information regarding mortalities or
sublethal effects of strychnine or other
banned pesticides on sage-grouse.
Although a reduction in insect
population levels resulting from
insecticide application can potentially
affect nesting sage-grouse females and
chicks (Willis et al. 1993, p. 40;
Schroeder et al. 1999, p. 16), there is no
information as to whether insecticides
are impacting survivorship or
productivity of the Gunnison sagegrouse.
Herbicide applications can kill
sagebrush and forbs important as food
sources for sage-grouse (Carr 1968 in
Call and Maser 1985, p. 14). The greatest
impact resulting from a reduction of
either forbs or insect populations is to
nesting females and chicks due to the
loss of potential protein sources that are
critical for successful egg production
and chick nutrition (Johnson and Boyce
1991, p. 90; Schroeder et al. 1999, p.
16). A comparison of applied levels of
herbicides with toxicity studies of
grouse, chickens, and other gamebirds
(Carr 1968, in Call and Maser 1985, p.
15) concluded that herbicides applied at
recommended rates should not result in
sage-grouse poisonings.
Use of insecticides to control
mosquitoes is infrequent and probably
does not have detrimental effects on
sage-grouse. Available insecticides that
kill adult mosquitoes include synthetic
pyrethroids such as permethrin, which
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are applied at very low concentrations
and have very low vertebrate toxicity
(Rose 2004). Organophosphates such as
malathion have been used at very low
rates to kill adult mosquitoes for
decades, and are judged relatively safe
for vertebrates (Rose 2004).
In summary, historically insecticides
have been shown to result in direct
mortality of individuals, and also can
reduce the availability of food sources,
which in turn could contribute to
mortality of sage-grouse. Despite the
potential effects of pesticides, we could
find no information to indicate that the
use of these chemicals, at current levels,
negatively affects Gunnison sage-grouse
population numbers. Schroeder et al.’s
(1999, p. 16) literature review found that
the loss of insects can have significant
impacts on nesting females and chicks,
but those impacts were not detailed.
Many of the pesticides that have been
shown to have an effect on sage-grouse
have been banned in the United States
for more than 20 years. We currently do
not have any information to show that
either the illegal use of banned
pesticides or residues in the
environment are presently having
negative impacts to sage-grouse
populations. While the reduction in
insect availability via insecticide
application has not been documented to
affect overall population numbers in
sage-grouse, we believe that insect
reduction, because of its importance to
chick production and survival, could be
having as yet undetected negative
impacts in populations with low
population numbers. There is no
information available to indicate that
either herbicide or insecticide
applications pose a threat to the species
now or in the foreseeable future.
Contaminants
Gunnison sage-grouse exposure to
various types of environmental
contaminants may potentially occur as a
result of agricultural and rangeland
management practices, mining, energy
development and pipeline operations,
and transportation of materials along
highways and railroads.
We expect that the number of sagegrouse occurring in the immediate
vicinity of wastewater pits associated
with energy development would be
small due to the small amount of energy
development within the species’ range,
the typically intense human activity in
these areas, the lack of cover around the
pits, and the fact that sage-grouse do not
require free water. Most bird mortalities
recorded in association with wastewater
pits are water-dependent species (e.g.,
waterfowl), whereas dead grounddwelling birds (such as the sage-grouse)
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are rarely found at such sites (Domenici
2008, pers. comm.). However, if the
wastewater pits are not appropriately
screened, sage-grouse may have access
to them and could ingest water and
become oiled while pursing insects. If
these birds then return to sagebrush
cover and die, their carcasses are
unlikely to be found as only the pits are
surveyed.
A few gas and oil pipelines occur
within the San Miguel population.
Exposure to oil or gas from pipeline
spills or leaks could cause mortalities or
morbidity to Gunnison sage-grouse.
Similarly, given the network of
highways and railroad lines that occur
throughout the range of the Gunnison
sage-grouse, there is some potential for
exposure to contaminants resulting from
spills or leaks of hazardous materials
being conveyed along these
transportation corridors. We found no
documented occurrences of impacts to
Gunnison sage-grouse from such spills,
and we do not expect they are a
significant source of mortality and a
threat to the species because these types
of spills occur infrequently and may
involve only a small area within the
occupied range of the species.
Summary of Factor E
Although genetic consequences of low
Gunnison sage-grouse population
numbers have not been definitively
detected to date, the results from Stiver
et al. (2008, p. 479) suggest that six of
the seven populations may have
effective sizes low enough to induce
inbreeding depression and all seven
could be losing adaptive potential.
While some of these consequences may
be ameliorated by translocations, we
believe the long-term viability of
Gunnison sage-grouse is compromised
by this situation, particularly when
combined with threats discussed under
other Factors, and we have determined
that genetics risks related to the small
population size of Gunnison sage-grouse
are a threat to the species now and in
the foreseeable future.
While sage-grouse have evolved with
drought, population numbers suggest
that drought is at least correlated with,
and potentially an underlying cause of,
the declines. Although we cannot
determine whether drought alone is a
threat to the species, we believe it is an
indirect threat exacerbating other threat
factors such as predation or habitat
fragmentation. Based on the available
information, insecticides are being used
infrequently enough and in accordance
with manufacturer labeling such that
they are not adversely affecting
populations of the Gunnison sagegrouse. The most likely impact of
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pesticides on Gunnison sage-grouse is
the reduction of insect prey items.
However, we could find no information
to indicate that use of pesticides, in
accordance with their label instructions,
is a threat to Gunnison sage-grouse.
Thus, based on the best scientific and
commercial data available, we have
concluded that other natural or
manmade factors are a significant threat
to the Gunnison sage-grouse.
Finding
We have carefully assessed the best
scientific and commercial information
available regarding the present and
future threats to the Gunnison sagegrouse. We have reviewed the
information available in our files,
information received during the
comment period, and other published
and unpublished information, and
consulted with recognized Gunnisonsage grouse and sagebrush habitat
experts. On the basis of the best
scientific and commercial information
available, we find that listing of the
Gunnison sage-grouse is warranted
throughout all of its range.
Gunnison sage-grouse, a sagebrush
obligate, are a landscape-scale species
requiring large, contiguous areas of
sagebrush for long-term persistence.
Gunnison sage-grouse occur in seven
isolated and fragmented populations,
primarily in southwestern Colorado,
with a small portion of its range
extending into southeastern Utah.
Populations have been declining since
the 1960s, with the Gunnison Basin
population the only relatively stable
population. Six of the seven remaining
populations are now small enough to be
vulnerable to extirpation (Stiver et al.
2008, p. 479). Specific issues identified
under Factors A, C, D, and E are threats
to the Gunnison sage-grouse. These
threats are exacerbated by small
population sizes, the isolated and
fragmented nature of the remaining
sagebrush habitat, and the potential
effects of climate change.
Current and future direct and
functional loss of habitat due to
residential and road development in all
populations (as discussed in Factor A)
is the principal threat to the Gunnison
sage-grouse. Other threats from human
infrastructure such as fences and
powerlines (as discussed in Factor A)
may not individually threaten the
Gunnison sage-grouse; however, the
cumulative presence of these features,
particularly when considered with
residential and road development, do
constitute a threat to the continued
existence of the Gunnison sage-grouse
as they collectively contribute to habitat
loss and fragmentation. These impacts
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exacerbate the fragmentation that has
already occurred in Gunnison sagegrouse habitat from past agricultural
conversion and residential
development. Gunnison sage-grouse are
sensitive to these forms of habitat
fragmentation because they require large
areas of contiguous, suitable habitat.
Given the increasing human population
trends in Gunnison sage-grouse habitat,
we expect urban and exurban
development and associated roads and
infrastructure to continue to expand.
Likewise, we expect direct and indirect
effects from these activities, including
habitat loss, degradation and
fragmentation, to increase in sage-grouse
habitats.
Invasive species, fire, and climate
change (as discussed in Factor A) may
not individually threaten the Gunnison
sage-grouse; however, the documented
synergy among these factors result in a
high likelihood that they will threaten
the species in the future. Noxious and
invasive plant incursions into sagebrush
ecosystems, which are facilitated by
human activities and fragmentation, are
likely to increase wildfire frequencies,
further contributing to direct loss of
habitat and fragmentation. Climate
change may alter the range of invasive
plants, intensifying the proliferation of
invasive plants to the point that they
become a threat to the species. While
recent local climatic moderations may
have produced some improved habitat
quality (increased forb and grass growth
providing enhanced grouse productivity
and survival). Habitat conservation
efforts have been implemented to
benefit local habitat conditions, but they
have not cumulatively resulted in local
population recoveries because
unfragmented sagebrush habitats on the
scale required that contain the necessary
ecological attributes (e.g., connectivity
and landscape context) have been lost.
Sagebrush habitats are highly
fragmented due to anthropogenic
impacts, and in most cases are not
resilient enough to return to native
vegetative states following disturbance
from fire, invasive species, and the
effects of climate change. We expect
these threats to continue and potentially
increase in magnitude in the future.
We found no evidence that the threats
summarized above, which contribute to
habitat loss, degradation and
fragmentation will subside within the
foreseeable future. Six populations are
extremely small and compromised by
existing fragmentation. The one
remaining relatively contiguous patch of
habitat (Gunnison Basin) for the species
is somewhat compromised by existing
fragmentation. Based on the current and
anticipated habitat threats and their
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cumulative effects as they contribute to
the overall fragmentation of Gunnison
sage-grouse habitat, we have determined
that threats identified under Factor A
pose a significant threat to the species
throughout its range. We find that the
present or threatened destruction,
modification, or curtailment of
Gunnison sage-grouse habitat is a threat
to the species future existence.
We believe that existing and
continued landscape fragmentation will
increase the effects of predation
(discussed in Factor C above) on this
species, particularly in the six smaller
populations, resulting in a reduction in
sage-grouse productivity and abundance
in the future. Predation has a strong
relationship with anthropogenic factors
on the landscape, and human presence
on the landscape will continue to
increase in the future. We find that
predation is a significant threat to the
species.
West Nile virus (discussed in Factor
C above) is the only disease that
currently presents a potential threat to
the Gunnison sage-grouse. While we
have no evidence of West Nile virus
acting on the Gunnison sage-grouse,
because of the virus’s presence within
the species’ range and the continued
development of anthropogenic water
sources in the area, the virus may pose
a future threat to the species. We have
determined that disease is not currently
a threat to the species. However, we
anticipate that West Nile virus will
persist within the range of Gunnison
sage-grouse indefinitely and will be
exacerbated by factors such as climate
change that could increase ambient
temperatures and the presence of the
vector on the landscape.
An examination of regulatory
mechanisms (discussed in Factor D
above) for both the Gunnison sagegrouse and sagebrush habitats revealed
that while limited mechanisms exist,
they are not broad enough in their
potential conservation value throughout
the species range, and are not being
implemented consistent with our
current understanding of the species’
biology and reaction to disturbances, to
be effective at ameliorating threats. This
is particularly true on private lands,
which comprise 41 percent of the
species’ extant range and are highly
dispersed throughout all populations.
Inadequate regulation of grazing
practices on public land is occurring in
some locations within the species’
range. Public land management agencies
should continue to improve habitat
conditions to be compatible with
Gunnison sage-grouse life-history
requirements. Some local conservation
efforts are effective and should be
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continued, but to date have occurred on
a scale that is too small to remove
threats at a range-wide level. Many
conservation efforts lacked sufficient
monitoring to demonstrate their overall
effectiveness in minimizing or
eliminating the primary threat of habitat
loss, fragmentation, and degradation.
Therefore, we find the existing
regulatory mechanisms are ineffective at
ameliorating habitat-based threats.
Small population size and genetic
factors (discussed in Factor E above)
subject at least six of the seven
populations to a high risk of extirpation
from stochastic events. All populations
are currently isolated as documented by
low amounts of gene flow (OylerMcCance et al. 2005, p. 635). The loss
of connectivity and the concomitant
isolation of the populations also
increase the species’ extinction risk.
Fitness and population size are strongly
correlated, and smaller populations are
more subject to environmental and
demographic stochasticity. When
coupled with mortality stressors related
to human activity and significant
fluctuations in annual population size,
long-term persistence of small
populations is always problematic.
Given the species’ relatively low rate of
growth and strong site fidelity, recovery
and repopulation of extirpated, or
nearly extirpated areas, will be
extremely challenging. Translocation of
Gunnison sage-grouse is difficult and to
date has not been demonstrated to be
successful in maintaining and
improving population and species
viability. Given the limited number of
source individuals, sustainable,
successful translocation efforts
involving large numbers of individuals
are unlikely at this time. Recent captiverearing efforts by CDOW have provided
some optimistic results. Nonetheless,
even assuming CDOW captive-rearing
and tranlocation efforts prove to be
successful in the long-term, the existing
condition of the habitat throughout the
species’ range will need to be improved,
before captive rearing and translocation
can be relied on to maintain population
and species viability.
The existing and continuing loss,
degradation, and fragmentation of sagegrouse habitat; extremely small
population sizes; occupancy of
extremely small, isolated, and
fragmented sagebrush areas; increased
susceptibility to predation; lack of
interconnectivity; low genetic diversity;
and the potential for catastrophic
stochastic (random) events, combined
with the inadequacy of existing
regulations to manage habitat loss
(either direct or functional), endanger
all Gunnison sage-grouse populations
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and the species as a whole. Threat
factors affecting the Gunnison sagegrouse are summarized in Table 5
below. As required by the Act, we have
reviewed and taken into account efforts
being made to protect Gunnison sagegrouse. Although some local
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conservation efforts have been
implemented and are effective in small
areas, they are not at a scale that is
sufficient to ameliorate threats to the
species as a whole. Other conservation
efforts (such as habitat treatments,
establishment of conservation
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easements, improved grazing practices,
additional travel management efforts
that benefit Gunnison sage-grouse) are
being planned, but there is substantial
uncertainty as to whether, where, and
when they will be implemented, and
whether they will be effective.
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28SEP2
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Threat or Impact
A
Residential Development
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Fire
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˜
Pinon-Juniper Encroachment
A
28SEP2
Domestic and Wild Ungulate
Herbivory
A
Invasive Plants
A
Powerlines
A
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A
Roads
A
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Fences
A
Water Development
A
Listing Factor
A
High
Low
Moderate
Low
Moderate
High+
Moderate
High+
Low
Moderate
Overall
Magnitude
Low
Low
Moderate
Low
Moderate
High
Low
High
Low
Moderate
Intensity
Magnitude
85%
15%
65%
10%
60%
90%
75%
70%
<20%
40%
Exposure
(percent)
Imminent
Imminent
Imminent
Non-Imminent
Imminent
Imminent
Imminent
Imminent
Non-Imminent
Non-Imminent
Overall Imminence
Moderate
Moderate
Moderate
Low
High
High
High
High
Low
Low
Likelihood
Imminence
Habitat degradation
Habitat fragmentation and
degradation; increased
predation
Habitat loss, fragmentation,
and degradation
Habitat loss, fragmentation,
and degradation
Habitat loss, fragmentation
and degradation;
increased predation
Habitat loss, fragmentation
and degradation;
increased predation; direct
mortality
Habitat fragmentation and
degradation; increased
predation; direct mortality
Habitat loss, fragmentation
and degradation;
increased predation
Past development
contributes to habitat
fragmentation and degradation
Past conversion contributes
to current habitat
fragmentation and
degradation.
Species’ Response
Indefinitely
Indefinitely
Likely to
increase
indefinitely
due to
increased
human
presence
and climate
change
Likely to
increase
indefinitely
with
cheatgrass
invasion
Year 2050
Year 2050
Year 2050
Year 2050
Year 2050
Year 2050a
Foreseeable
Future
TABLE 5. THREAT SUMMARY FOR FACTORS AFFECTING GUNNISON SAGE-GROUSE. A ‘‘+’’ INDICATES HIGHER LEVEL OF THREAT.
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Moderate
Low
Moderate+
Low+
Moderate+
High
Moderate
High
Low
Low
Overall Threat
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53).
a
Non-renewable Energy
Development
Hunting
Climate Change
Disease
Predation
Inadequacy of Local Laws and
Regulations
B
C
C
D
Inadequacy of State Laws and
Regulations
Scientific Research
B
E
Small Population Size
Genetic Complications
D
Recreation
Pesticides and Herbicides
Contaminants
E
E
E
E
Low
Low
Low
Moderate+
Moderate+
High
High
Moderate
High
High
Low
Low+
Low
Low
Low
Low+
Low+
Overall
Magnitude
Low
Low
Low+
High
Moderate+
Moderate+
High
High
Moderate
Moderate+
Low
Low+
Low
Low
Moderate
Low+
Moderate
Intensity
Magnitude
<5%
10%
50%
100%
60%
70%
75%
60%
50%
90%
100%
50%
10%
0%
100%
15%
10%
Exposure
(percent)
Non-Imminent
Non-Imminent
Imminent
Imminent
Imminent
Imminent
Imminent
Imminent
Imminent
Imminent
Non-Imminent
Imminent
Imminent
Non-Imminent
Imminent
Non-Imminent
Imminent
Overall Imminence
Low
Low
Moderate
Moderate
High
High
High
High
High
High
Moderate
Moderate
Moderate
Low
Moderate
Moderate
Low
Likelihood
Imminence
Direct mortality
Direct mortality; habitat
degradation
Harassment; avoidance
Habitat degradation; decline
in species reproductive
potential
Population vulnerability to
stochastic events
Inbreeding depression; loss
of adaptive potential
Habitat loss, fragmentation,
and degradation
Habitat loss, fragmentation,
and degradation
Habitat loss, fragmentation,
and degradation
Direct mortality
Direct mortality
Harassment; direct mortality
Harassment; avoidance
None
Unknown, but could facilitate increase in invasive
plants and corresponding
increased fire
frequency
Habitat fragmentation and
degradation; increased
predation
Habitat fragmentation and
degradation; increased
predation
Species’ Response
Year 2050
Year 2050
Year 2050
Indefinitely
Indefinitely
Indefinitely
Year 2050
Year 2050
Year 2050
Indefinitely
Indefinitely
Year 2050
Year 2050
Year 2050
Climate
models
predict out to
40 years
Year 2050
Year 2050
Foreseeable
Future
Low
Low
Low
Moderate
Moderate+
High
High
Moderate
High
Moderate+
Low
Low
Low
Low
Low
Low
Low
Overall Threat
The foreseeable future date of 2050 was determined for threats or impacts directly related to anthropogenic activities based on the furthest population projection from CWCB (2009, p.
Drought
E
Inadequacy of Federal Laws
and Regulations
D
Lek Viewing
B
A
Energy
Renewable
ment
A
Develop-
Threat or Impact
A
Listing Factor
TABLE 5. THREAT SUMMARY FOR FACTORS AFFECTING GUNNISON SAGE-GROUSE. A ‘‘+’’ INDICATES HIGHER LEVEL OF THREAT.—Continued
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Listing factors include: (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.
We have carefully assessed the best
scientific and commercial information
available regarding the present and
future threats to the Gunnison sagegrouse. We have reviewed petitions,
information available in our files, and
other published and unpublished
information, and consulted with
recognized Gunnison sage-grouse and
greater sage-grouse experts. We have
considered and taken into account
efforts being made to conserve protect
the species. On the basis of the best
scientific and commercial information
available, we find that listing of the
Gunnison sage-grouse is warranted
throughout all of its range. However,
listing the Gunnison sage-grouse is
precluded by higher priority listing
actions at this time, as discussed in the
Preclusion and Expeditious Progress
section below.
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Listing Priority Number
The Service adopted guidelines on
September 21, 1983 (48 FR 43098), to
establish a rational system for utilizing
available resources for the highest
priority species when adding species to
the Lists of Endangered or Threatened
Wildlife and Plants or reclassifying
species listed as threatened to
endangered status. These guidelines,
titled ‘‘Endangered and Threatened
Species Listing and Recovery Priority
Guidelines’’ address the immediacy and
magnitude of threats, and the level of
taxonomic distinctiveness by assigning
priority in descending order to
monotypic genera (genus with one
species), full species, and subspecies (or
equivalently, distinct population
segments of vertebrates).
As a result of our analysis of the best
available scientific and commercial
information, we assigned the Gunnison
sage-grouse an LPN of 2 based on our
finding that the species faces threats
that are of high magnitude and are
imminent. These threats include the
present or threatened destruction,
modification, or curtailment of its
habitat; predation; the inadequacy of
existing regulatory mechanisms; and
other natural or man-made factors
affecting its continued existence. Our
rationale for assigning the Gunnison
sage-grouse an LPN 2 is outlined below.
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Under the Service’s LPN Guidance,
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. We consider the
threats that the Gunnison sage-grouse
faces to be high in magnitude because
the major threats (exurban development,
inadequacy of regulatory mechanisms,
genetic issues, roads) occur throughout
all of the species range. Based on an
evaluation of biotic, abiotic, and
anthropogenic factors, no strongholds
are believed to exist for Gunnison sagegrouse (Wisdom et al., in press, entire).
All seven populations are experiencing
habitat degradation and fragmentation
due to exurban development and roads.
Six of the seven populations of
Gunnison sage-grouse currently contain
so little occupied habitat that continued
degradation and fragmentation will
place their continued existence in
question. The remaining population
(Gunnison Basin) is so interspersed with
development and roads that it is likely
to degrade and fragment the habitat
(Aldridge and Saher, in press, entire).
We believe it is not functional for a
species that requires large expanses of
sagebrush. Six of the seven populations
of Gunnison sage-grouse have
population sizes low enough to induce
inbreeding depression, and all seven
may be losing their adaptive potential
(Stiver 2008, p. 479). Predation is
exerting a strong influence on all
populations, but especially the six
smaller populations. Invasive weeds are
likely to exert a strong influence on all
populations in the future. Adequate
regulations are not in place at the local,
State, or Federal level to adequately
minimize the threat of habitat
degradation and fragmentation resulting
from exurban development. Regulatory
mechanisms are not being appropriately
implemented such that land use
practices result in habitat conditions
that adequately support the life-history
needs of the species. Adequate
regulations are also not in place to
ameliorate the threats resulting from
predation, genetic issues, or invasive
weeds. Due to the impacts resulting
from the issues described above and the
current small population sizes and
habitat areas, impacts from other
stressors such as fences, recreation,
grazing, powerlines, and drought/
weather are likely acting cumulatively
to further decrease the likelihood of at
least the six small populations, and
potentially all seven, persisting into the
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59853
future. We believe the ability of all
remaining populations and habitat areas
to retain the attributes required for longterm sustainability of this landscapescale species are highly diminished
indicating that the magnitude of threats
is high.
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 great
detail in Factors A, C, D, and E of this
finding and currently include habitat
degradation and fragmentation from
exurban development and roads,
inadequate regulatory mechanisms,
genetic issues, predation, invasive
plants, and drought/weather. In
addition to their current existence, we
expect these threats to continue and
likely intensify in the foreseeable future.
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 Gunnison
sage-grouse is a valid taxon at the
species level, and therefore receives a
higher priority than subspecies or DPSs,
but a lower priority than species in a
monotypic genus.
We will continue to monitor the
threats to the Gunnison sage-grouse, and
the species’ status on an annual basis,
and should the magnitude or the
imminence of the threats change, we
will re-visit our assessment of LPN.
Currently, work on a proposed listing
determination for the Gunnison sagegrouse is precluded by work on higher
priority listing actions with absolute
statutory, court-ordered, or courtapproved deadlines and final listing
determinations for those species that
were proposed for listing with funds
from FY 2009. Additionally, remaining
listing funding from FY 2010 has been
directed to work on listing
determinations for species at
significantly greater risk of extinction
than the Gunnison sage-grouse faces.
Because of the large number of highpriority species, we further ranked the
candidate species with an LPN of 2. The
resulting ‘‘Top 40’’ list of candidate
species have the highest priority to
receive funding to work on a proposed
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listing determination (see the Preclusion
and Expeditious Progress section
below). This work includes all the
actions listed in the tables below under
expeditious progress.
Preclusion and Expeditious Progress
Preclusion is a function of the listing
priority of a species in relation to the
resources that are available and
competing demands for those resources.
Thus, in any given fiscal year (FY),
multiple factors dictate whether it will
be possible to undertake work on a
proposed listing regulation or whether
promulgation of such a proposal is
warranted but precluded by higherpriority listing actions.
The resources available for listing
actions are determined through the
annual Congressional appropriations
process. The appropriation for the
Service 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
complexity of those listing actions; that
is, more complex actions generally are
more costly. The median cost for
preparing and publishing a 90–day
finding is $39, 276; for a 12–month
finding, $100,690; for a proposed rule
with critical habitat, $345,000; and for
a final listing rule with critical habitat,
the median cost is $305,000.
We cannot spend more than is
appropriated for the Listing Program
without violating the Anti-Deficiency
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Act (see 31 U.S.C. 1341(a)(1)(A)). In
addition, in FY 1998 and for each fiscal
year since then, Congress has placed a
statutory cap on funds which may be
expended for the Listing Program, equal
to the amount expressly appropriated
for that purpose in that fiscal year. This
cap was designed to prevent funds
appropriated for other functions under
the Act (for example, recovery funds for
removing species from the Lists), or for
other Service programs, from being used
for Listing Program actions (see House
Report 105-163, 105th Congress, 1st
Session, July 1, 1997).
Since FY 2002, the Service’s budget
has included a critical habitat subcap to
ensure that some funds are available for
other work in the Listing Program (‘‘The
critical habitat designation subcap will
ensure that some funding is available to
address other listing activities’’ (House
Report No. 107 - 103, 107th Congress, 1st
Session, June 19, 2001)). In FY 2002 and
each year until FY 2006, the Service has
had to use virtually the entire critical
habitat subcap to address courtmandated designations of critical
habitat, and consequently none of the
critical habitat subcap funds have been
available for other listing activities. In
FY 2007, we were able to use some of
the critical habitat subcap funds to fund
proposed listing determinations for
high-priority candidate species. 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
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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
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 highpriority listing actions at this time,
many actions have statutory or court-
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approved settlement deadlines, thus
increasing their priority. The allocations
for each specific listing action are
identified in the Service’s FY 2010
Allocation Table (part of our
administrative record).
Based on our September 21, 1983,
guidance for assigning an LPN for each
candidate species (48 FR 43098), we
have a significant number of species
with a LPN of 2. Using this guidance,
we assign each candidate an LPN of 1
to 12, depending on the magnitude of
threats (high vs. moderate to low),
immediacy of threats (imminent or
nonimminent), and taxonomic status of
the species (in order of priority:
monotypic genus (a species that is the
sole member of a genus); species; or part
of a species (subspecies, distinct
population segment, or significant
portion of the range)). The lower the
listing priority number, the higher the
listing priority (that is, a species with an
LPN of 1 would have the highest listing
priority). Because of the large number of
high-priority species, we have 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, originally 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 those
40 candidates, we apply 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 the highest priority species in the
next several years, we are preparing
multi-species proposals when
appropriate, and these may include
species with lower priority if they
overlap geographically or have the same
threats as a species with an LPN of 2.
In addition, available staff resources are
also a factor in determining highpriority species provided with funding.
Finally, proposed rules for
reclassification of threatened species to
endangered are lower priority, since as
listed species, they are already afforded
the protection of the Act and
implementing regulations.
We assigned the Gunnison sagegrouse an LPN of 2, based on our
finding that the species faces immediate
and high magnitude threats from the
present or threatened destruction,
modification, or curtailment of its
habitat; predation; the inadequacy of
existing regulatory mechanisms; and
other natural or man-made factors
affecting its continued existence. One or
more of the threats discussed above
occurs in each known population. These
threats are ongoing and, in some cases,
considered irreversible. Under our 1983
Guidelines, a ‘‘species’’ facing imminent
high-magnitude threats is assigned an
LPN of 1, 2, or 3 depending on its
taxonomic status. Because the Gunnison
sage-grouse is a species, we assigned it
an LPN of 2 (the highest category
available for a species). Therefore, work
on a proposed listing determination for
the Gunnison sage-grouse is precluded
by work on higher priority candidate
species; listing actions with absolute
statutory, court ordered, or courtapproved deadlines; and final listing
determinations for those species that
were proposed for listing with funds
from previous fiscal years. This work
includes all the actions listed in the
tables below under expeditious
progress.
As explained above, a determination
that listing is warranted but precluded
must also demonstrate that expeditious
progress is being made to add or remove
qualified species to and from the Lists
of Endangered and Threatened Wildlife
and Plants. (Although we do not discuss
it in detail here, we are also making
expeditious progress in removing
species from the 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:
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
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10/08/2009
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
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FY 2010 COMPLETED LISTING ACTIONS—Continued
Publication Date
Title
Actions
FR Pages
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 sagegrouse (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
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
1/05/2010
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
WReier-Aviles on DSKGBLS3C1PROD with PROPOSALS2
11/03/2009
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
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FY 2010 COMPLETED LISTING ACTIONS—Continued
Title
Actions
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 ListingEndangered
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
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
WReier-Aviles on DSKGBLS3C1PROD with PROPOSALS2
Publication Date
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
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
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FY 2010 COMPLETED LISTING ACTIONS—Continued
Title
Actions
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
6/1/2010
90-Day Finding on a Petition To List
Castanea pumila var. ozarkensis
Notice of 90–day Petition Finding,
Substantial
75 FR 30313-30318
6/1/2010
12–month Finding on a Petition to
List the White-tailed Prairie Dog as
Endangered or Threatened
Notice of 12–month petition finding,
Not warranted
75 FR 30338-30363
6/9/2010
90-Day Finding on a Petition To List
van Rossem’s Gull-billed Tern as
Endangered orThreatened.
Notice of 90–day Petition Finding,
Substantial
75 FR 32728-32734
6/16/2010
90-Day Finding on Five Petitions to
List Seven Species of Hawaiian
Yellow-faced Bees as Endangered
Notice of 90–day Petition Finding,
Substantial
75 FR 34077-34088
6/22/2010
12-Month Finding on a Petition to List
the Least Chub as Threatened or
Endangered
Notice of 12–month petition finding,
Warranted but precluded
75 FR 35398-35424
6/23/2010
90-Day Finding on a Petition to List
the Honduran Emerald
Hummingbird as Endangered
Notice of 90–day Petition Finding,
Substantial
75 FR 35746-35751
6/23/2010
Listing Ipomopsis polyantha (Pagosa
Skyrocket)
as
Endangered
Throughout Its Range, and Listing
Penstemon
debilis
(Parachute
Beardtongue)
and
Phacelia
submutica (DeBeque Phacelia) as
Threatened
Throughout
Their
Range
Proposed Listing Endangered Proposed Listing Threatened
75 FR 35721-35746
6/24/2010
Listing the Flying Earwig Hawaiian
Damselfly and Pacific Hawaiian
Damselfly As Endangered
Throughout Their Ranges
Final Listing Endangered
75 FR 35990-36012
6/24/2010
Listing the Cumberland Darter, Rush
Darter, Yellowcheek Darter, Chucky
Madtom, and Laurel Dace as
Endangered
Throughout
Their
Ranges
Proposed Listing Endangered
75 FR 36035-36057
6/29/2010
Listing the Mountain
Threatened
as
Reinstatement of Proposed Listing
Threatened
75 FR 37353-37358
7/20/2010
90-Day Finding on a Petition to List
Pinus albicaulis (Whitebark Pine)
as Endangered or Threatened with
Critical Habitat
Notice of 90–day Petition Finding,
Substantial
75 FR 42033-42040
7/20/2010
WReier-Aviles on DSKGBLS3C1PROD with PROPOSALS2
Publication Date
12-Month Finding on a Petition to List
the Amargosa Toad as Threatened
or Endangered
Notice of 12–month petition finding,
Not warranted
75 FR 42040-42054
7/20/2010
90-Day Finding on a Petition to List
the Giant Palouse Earthworm
(Driloleirus americanus) as
Threatened or Endangered
Notice of 90–day Petition Finding,
Substantial
75 FR 42059-42066
7/27/2010
Determination on Listing the BlackBreasted Puffleg as Endangered
Throughout its Range; Final Rule
Final Listing Endangered
75 FR 43844-43853
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59859
FY 2010 COMPLETED LISTING ACTIONS—Continued
Publication Date
Title
Actions
FR Pages
Final Rule to List the Medium TreeFinch (Camarhynchus pauper) as
Endangered Throughout Its Range
Final Listing Endangered
75 FR 43853-43864
8/3/2010
Determination of Threatened Status
for Five Penguin Species
Final ListingThreatened
75 FR 45497- 45527
8/4/2010
90-Day Finding on a Petition To List
the Mexican Gray Wolf as an
Endangered Subspecies With Critical
Habitat
Notice of 90–day Petition Finding,
Substantial
75 FR 46894- 46898
8/10/2010
90-Day Finding on a Petition to List
Arctostaphylos franciscana as
Endangered with Critical Habitat
Notice of 90–day Petition Finding,
Substantial
75 FR 48294-48298
8/17/2010
Listing Three Foreign Bird Species
from Latin America and the
Caribbean as Endangered
Throughout Their Range
Final Listing Endangered
75 FR 50813-50842
8/17/2010
90-Day Finding on a Petition to List
Brian Head Mountainsnail as
Endangered or Threatened with
Critical Habitat
Notice of 90–day Petition Finding, Not
substantial
75 FR 50739-50742
8/24/2010
90-Day Finding on a Petition to List
the Oklahoma Grass Pink Orchid
as Endangered or Threatened
Notice of 90–day Petition Finding,
Substantial
75 FR 51969-51974
9/1/2010
12-Month Finding on a Petition to List
the White-Sided Jackrabbit as
Threatened or Endangered
Notice of 12–month petition finding,
Not warranted
75 FR 53615-53629
9/8/2010
Proposed Rule To List the Ozark
Hellbender Salamander as
Endangered
Proposed Listing Endangered
75 FR 54561-54579
9/8/2010
Revised 12-Month Finding to List the
Upper Missouri River Distinct
Population
Segment
of
Arctic
Grayling as Endangered or
Threatened
Notice of 12–month petition finding,
Warranted but precluded
75 FR 54707-54753
9/9/2010
WReier-Aviles on DSKGBLS3C1PROD with PROPOSALS2
7/27/2010
12-Month Finding on a Petition to List
the Jemez Mountains Salamander
(Plethodon neomexicanus) as
Endangered or Threatened with
Critical Habitat
Notice of 12–month petition finding,
Warranted but precluded
75 FR 54822-54845
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.
ACTIONS FUNDED IN FY 2010 BUT NOT YET COMPLETED
Species
Action
Actions Subject to Court Order/Settlement Agreement
6 Birds from Eurasia
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Federal Register / Vol. 75, No. 187 / Tuesday, September 28, 2010 / Proposed Rules
ACTIONS FUNDED IN FY 2010 BUT NOT YET COMPLETED—Continued
Species
Action
African penguin
Final listing determination
Flat-tailed horned lizard
Final listing determination
Mountain plover4
Final listing determination
6 Birds from Peru
Proposed listing determination
Sacramento splittail
12–month petition finding
Pacific walrus
12–month petition finding
Gunnison sage-grouse
12–month petition finding
Wolverine
12–month petition finding
Agave eggergsiana
12–month petition finding
Solanum conocarpum
12–month petition finding
Sprague’s pipit
12–month petition finding
Desert tortoise – Sonoran population
12–month petition finding
Pygmy rabbit (rangewide)1
12–month petition finding
Thorne’s Hairstreak butterfly3
12–month petition finding
Hermes copper butterfly3
12–month petition finding
Actions with Statutory Deadlines
Casey’s june beetle
Final listing determination
Georgia pigtoe, interrupted rocksnail, and rough hornsnail
Final listing determination
7 Bird species from Brazil
Final listing determination
Southern rockhopper penguin – Campbell Plateau population
Final listing determination
5 Bird species from Colombia and Ecuador
Final listing determination
Queen Charlotte goshawk
Final listing determination
5 species southeast fish (Cumberland darter, rush darter, yellowcheek
darter, chucky madtom, and laurel dace)
Final listing determination
Salmon crested cockatoo
Proposed listing determination
CA golden trout
12–month petition finding
Black-footed albatross
12–month petition finding
Mount Charleston blue butterfly
12–month petition finding
Mojave fringe-toed
lizard1
12–month petition finding
12–month petition finding
Cactus ferruginous pygmy-owl1
WReier-Aviles on DSKGBLS3C1PROD with PROPOSALS2
Kokanee – Lake Sammamish population1
12–month petition finding
Northern leopard frog
12–month petition finding
Tehachapi slender salamander
12–month petition finding
Coqui Llanero
12–month petition finding
Dusky tree vole
12–month petition finding
3 MT invertebrates (mist forestfly(Lednia tumana), Oreohelix sp.3,
Oreohelix sp. 31) from 206 species petition
12–month petition finding
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Federal Register / Vol. 75, No. 187 / Tuesday, September 28, 2010 / Proposed Rules
ACTIONS FUNDED IN FY 2010 BUT NOT YET COMPLETED—Continued
Species
Action
5 UT plants (Astragalus hamiltonii, Eriogonum soredium, Lepidium
ostleri, Penstemon flowersii, Trifolium friscanum) from 206 species
petition
12–month petition finding
2 CO plants (Astragalus microcymbus, Astragalus schmolliae) from 206
species petition
12–month petition finding
5 WY plants (Abronia ammophila, Agrostis rossiae, Astragalus
proimanthus, Boechere (Arabis) pusilla, Penstemon gibbensii) from
206 species petition
12–month petition finding
Leatherside chub (from 206 species petition)
12–month petition finding
Frigid ambersnail (from 206 species petition)
12–month petition finding
Gopher tortoise – eastern population
12–month petition finding
Wrights marsh thistle
12–month petition finding
67 of 475 southwest species
12–month petition finding
Grand Canyon scorpion (from 475 species petition)
12–month petition finding
Anacroneuria wipukupa (a stonefly from 475 species petition)
12–month petition finding
Rattlesnake-master borer moth (from 475 species petition)
12–month petition finding
3 Texas moths (Ursia furtiva, Sphingicampa blanchardi, Agapema
galbina) (from 475 species petition)
12–month petition finding
2 Texas shiners (Cyprinella sp., Cyprinella lepida) (from 475 species
petition)
12–month petition finding
3 South Arizona plants (Erigeron piscaticus, Astragalus hypoxylus,
Amoreuxia gonzalezii) (from 475 species petition)
12–month petition finding
5 Central Texas mussel species (3 from 474 species petition)
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
Fisher – Northern Rocky Mountain
Range1
12–month petition finding
12–month petition finding
Puerto Rico Harlequin Butterfly
12–month petition finding
Western gull-billed tern
12–month petition finding
Ozark chinquapin (Castanea pumila var. ozarkensis)
12–month petition finding
HI yellow-faced bees
12–month petition finding
Giant Palouse earthworm
12–month petition finding
Whitebark pine
12–month petition finding
OK grass pink (Calopogon oklahomensis)1
WReier-Aviles on DSKGBLS3C1PROD with PROPOSALS2
Mohave Ground Squirrel1
12–month petition finding
Southeastern pop snowy plover & wintering pop. of piping plover1
90–day petition finding
Eagle Lake
trout1
90–day petition finding
Smooth-billed ani1
90–day petition finding
Bay Springs salamander1
32 species of snails and
90–day petition finding
slugs1
90–day petition finding
42 snail species (Nevada & Utah)
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90–day petition finding
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Federal Register / Vol. 75, No. 187 / Tuesday, September 28, 2010 / Proposed Rules
ACTIONS FUNDED IN FY 2010 BUT NOT YET COMPLETED—Continued
Species
Action
Red knot roselaari subspecies
90–day petition finding
Peary caribou
90–day petition finding
Plains bison
90–day petition finding
Spring Mountains checkerspot butterfly
90–day petition finding
Spring pygmy sunfish
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
Golden-winged warbler
90–day petition finding
Sand-verbena moth
90–day petition finding
404 Southeast species
90–day petition finding
High-Priority Listing Actions3
19 Oahu candidate species2 (16 plants, 3 damselflies) (15 with LPN =
2, 3 with LPN = 3, 1 with LPN =9)
Proposed listing
19 Maui-Nui candidate species2 (16 plants, 3 tree snails) (14 with LPN
= 2, 2 with LPN = 3, 3 with LPN = 8)
Proposed listing
Dune sagebrush lizard (formerly Sand dune lizard)3 (LPN = 2)
Proposed listing
springsnails2
2 Arizona
trivialis (LPN = 2))
(Pyrgulopsis bernadina (LPN = 2), Pyrgulopsis
New Mexico springsnail2 (Pyrgulopsis chupaderae (LPN = 2)
2
mussels2
Proposed listing
Proposed listing
(rayed bean (LPN = 2), snuffbox No LPN)
Proposed listing
2 mussels2 (sheepnose (LPN = 2), spectaclecase (LPN = 4),)
Proposed listing
Altamaha spinymussel2 (LPN = 2)
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
1
Funds for listing actions for these species were provided in previous FYs.
Although funds for these high-priority listing actions were provided in FY 2008 or 2009, due to the complexity of these actions and competing
priorities, these actions are still being developed.
3Partially funded with FY 2010 funds; also will be funded with FY 2011 funds.
WReier-Aviles on DSKGBLS3C1PROD with PROPOSALS2
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
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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.
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The Gunnison sage-grouse 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
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WReier-Aviles on DSKGBLS3C1PROD with PROPOSALS2
warranted, including the need to make
prompt use of emergency listing
procedures.
We intend that any proposed listing
action for the Gunnison sage-grouse 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.
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References Cited
A complete list of references cited is
available on the Internet at https://
www.regulations.gov and upon request
from the Western Colorado Ecological
Services Field Office (see ADDRESSES
section).
Author(s)
The primary authors of this notice are
the staff members of the Western
Colorado Ecological Services Field
Office.
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59863
Authority
The authority for this section is
section 4 of the Endangered Species Act
of 1973, as amended (16 U.S.C. 1531 et
seq.).
Dated: September 7, 2010
Paul R. Schmidt,
Acting Director, Fish and Wildlife Service.
[FR Doc. 2010–23430 Filed 9–27–10; 8:45 am]
BILLING CODE 4310–55–S
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Agencies
[Federal Register Volume 75, Number 187 (Tuesday, September 28, 2010)]
[Proposed Rules]
[Pages 59804-59863]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2010-23430]
[[Page 59803]]
-----------------------------------------------------------------------
Part II
Department of the Interior
-----------------------------------------------------------------------
Fish and Wildlife Service
-----------------------------------------------------------------------
50 CFR Part 17
Endangered and Threatened Wildlife and Plants; Determination for the
Gunnison Sage-grouse as a Threatened or Endangered Species; Proposed
Rule
Federal Register / Vol. 75, No. 187 / Tuesday, September 28, 2010 /
Proposed Rules
[[Page 59804]]
-----------------------------------------------------------------------
DEPARTMENT OF THE INTERIOR
Fish and Wildlife Service
50 CFR Part 17
[DOCKET NO. FWS-R6-ES-2009-0080]
MO 92210-0-0008
Endangered and Threatened Wildlife and Plants; Determination for
the Gunnison Sage-grouse as a Threatened or Endangered Species
AGENCY: Fish and Wildlife Service, Interior.
ACTION: Notice of the results of a status review.
-----------------------------------------------------------------------
SUMMARY: We, the U.S. Fish and Wildlife Service (Service), announce our
12-month finding on whether to list the Gunnison sage-grouse
(Centrocercus minimus) as threatened or endangered under the Endangered
Species Act of 1973, as amended (Act). After reviewing the best
available scientific and commercial information, we find that the
species is warranted for listing. Currently, however, listing the
Gunnison sage-grouse is precluded by higher priority actions to amend
the Lists of Endangered and Threatened Wildlife and Plants. Upon
publication of this 12-month finding, we will add the Gunnison sage-
grouse to our candidate species list. We will develop a proposed rule
to list this species as our priorities allow. We will make any
determination on critical habitat during development of the proposed
listing rule.
DATES: The determination announced in this document was made on
September 28, 2010.
ADDRESSES: This finding is available on the Internet at https://www.regulations.gov at Docket Number FWS-R6-ES-2009-0080. 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, Western Colorado Ecological Services Field
Office, U.S. Fish and Wildlife Service, 764 Horizon Drive, Building B,
Grand Junction, Colorado 81506-3946. Please submit any new information,
materials, comments, or questions concerning this finding to the above
address.
FOR FURTHER INFORMATION CONTACT: Allan Pfister, Western Colorado
Supervisor (see ADDRESSES section); by telephone at (970) 243-2778 ext.
29; or by facsimile at (970) 245-6933. If you use a telecommunications
device for the deaf (TDD), please call the Federal Information Relay
Service (FIRS) at 800-877-8339.
SUPPLEMENTARY INFORMATION:
Background
Section 4(b)(3)(A) 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 that listing a species may be warranted, we make
a finding within 12 months of the date of receipt of the petition. In
this finding, we determine whether 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
On January 18, 2000, we designated the Gunnison sage-grouse as a
candidate species under the Act, with a listing priority number of 5.
However, Candidate Notices of Review (CNOR) are only published
annually; therefore, the Federal Register notice regarding this
decision was not published until December 28, 2000 (65 FR 82310).
Candidate species are plants and animals for which the Service has
sufficient information on their biological status and threats to
propose them as endangered or threatened under the Act, but for which
the development of a proposed listing regulation is precluded by other
higher priority listing activities. A listing priority of 5 is assigned
to species with high magnitude threats that are non-imminent.
On January 26, 2000, American Lands Alliance, Biodiversity Legal
Foundation, and others petitioned the Service to list the Gunnison
sage-grouse (Webb 2000, pp. 94-95). In 2003, the U.S. District Court
ruled that the species was designated as a candidate by the Service
prior to receipt of the petition, and that the determination that a
species should be on the candidate list is equivalent to a 12-month
finding (American Lands Alliance v. Gale A. Norton, C.A. No. 00-2339,
D. D.C.). Therefore, we did not need to respond to the petition.
In the 2003 CNOR, we elevated the listing priority number for
Gunnison sage-grouse from 5 to 2 (69 FR 24876; May 4, 2004), as the
imminence of the threats had increased. In the subsequent CNOR (70 FR
24870; May 11, 2005), we maintained the listing priority number for
Gunnison sage-grouse as a 2. A listing priority number of 2 is assigned
to species with high magnitude threats that are imminent.
Plaintiffs amended their complaint in May 2004, to allege that the
Service's warranted but precluded finding and decision not to emergency
list the Gunnison sage-grouse were in violation of the Act. The parties
filed a stipulated settlement agreement with the court on November 14,
2005, which included a provision that the Service would make a proposed
listing determination by March 31, 2006. On March 28, 2006, the
plaintiffs agreed to a one-week extension (April 7, 2006) for this
determination.
In April 2005, the Colorado Division of Wildlife (CDOW) applied to
the Service for an Enhancement of Survival Permit for the Gunnison
sage-grouse pursuant to section 10(a)(1)(A) of the Act. The permit
application included a proposed Candidate Conservation Agreement with
Assurances (CCAA) between CDOW and the Service. The standard that a
CCAA must meet is that the ``benefits of the conservation measures
implemented under a CCAA, when combined with those benefits that would
be achieved if it is assumed that conservation measures were also to be
implemented on other necessary properties, would preclude or remove any
need to list the species.'' The CCAA, the permit application, and the
Environmental Assessment were made available for public comment on July
6, 2005 (70 FR 38977). The CCAA and Environmental Assessment were
finalized in October 2006, and the associated permit was issued on
October 23, 2006. Landowners with eligible property in southwestern
Colorado who wish to participate can voluntarily sign up under the CCAA
and associated permit through a Certificate of Inclusion by providing
habitat protection or enhancement measures on their lands. If the
Gunnison sage-grouse is listed under the Act, the permit authorizes
incidental take of Gunnison sage-grouse due to otherwise lawful
activities in accordance with the terms of the CCAA (e.g., crop
cultivation, crop harvesting, livestock grazing, farm equipment
operation, commercial/residential development, etc.), as long as the
participating landowner is performing
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activities identified in the Certificate of Inclusion. Four
Certificates of Inclusion have been issued by the CDOW and Service to
private landowners to date.
On April 11, 2006, the Service determined that listing the Gunnison
sage-grouse as a threatened or endangered species was not warranted and
published the final listing determination in the Federal Register on
April 18, 2006 (71 FR 19954). Consequently, we removed Gunnison sage-
grouse from the candidate species list at the time of the final listing
determination. On November 14, 2006, Plaintiffs (the County of San
Miguel, Colorado; Center for Biological Diversity; WildEarth Guardians;
Public Employees for Environmental Responsibility; National Audubon
Society; The Larch Company; Center for Native Ecosystems; Sinapu;
Sagebrush Sea Campaign; Black Canyon Audubon Society; and Sheep
Mountain Alliance) filed a Complaint for Declaratory and Injunctive
relief, pursuant to the Act, and on October 24, 2007, filed an amended
Complaint for Declaratory and Injunctive relief, alleging that the 12-
month finding on the Gunnison sage-grouse violated the Act. On August
18, 2009, a stipulated settlement agreement and Order was filed with
the court, with a June 30, 2010, date by which the Service shall submit
to the Federal Register a 12-month finding, pursuant to 16 U.S.C. Sec.
1533(b)(3)(B), that listing the Gunnison sage-grouse under the Act is
(a) warranted; (b) not warranted; or (c) warranted but precluded by
higher priority listing actions. We published a notice of intent to
conduct a status review of Gunnison sage-grouse on November 23, 2009
(74 Fr 61100). The Court approved an extension of the June 30, 2010,
deadline for the 12-month finding to September 15, 2010.
Additional Special Status Considerations
The Gunnison sage-grouse has an International Union for
Conservation of Nature (IUCN) Red List Category of ``endangered''
(Birdlife International 2009). NatureServe currently ranks the Gunnison
sage-grouse as G1--Critically Imperiled (Nature Serve 2010, entire).
The Gunnison sage-grouse is on the National Audubon Society's WatchList
2007 Red Category which is ``for species that are declining rapidly or
have very small populations or limited ranges, and face major
conservation threats.''
Biology and Ecology of Gunnison Sage-grouse
Gunnison Sage-grouse Species Description
Sage-grouse are the largest grouse in North America. Sage-grouse
(both greater and Gunnison) are most easily identified by their large
size, dark brown color, distinctive black bellies, long pointed tails,
and association with sagebrush habitats. They are dimorphic in size,
with females being smaller. Both sexes have yellow-green eye combs,
which are less prominent in females. Sage-grouse are known for their
elaborate mating ritual where males congregate on strutting grounds
called leks and ``dance'' to attract a mate. During the breeding
season, males have conspicuous filoplumes (specialized erectile
feathers on the neck), and exhibit yellow-green apteria (fleshy bare
patches of skin) on their breasts (Schroeder et al. 1999, p. 2, 18).
Gunnison sage-grouse are smaller in size, have more white barring in
their tail feathers, and have more filoplumes than greater sage-grouse.
Since Gunnison and greater sage-grouse were only recognized as
separate species in 2000, the vast majority of the research relative to
the biology and management of the two species has been conducted on
greater sage-grouse. Gunnison sage-grouse and greater sage-grouse have
similar life histories and habitat requirements (Young 1994, p. 44). In
this finding, we use information specific to the Gunnison sage-grouse
where available but still apply scientific management principles found
relevant for greater sage-grouse to Gunnison sage-grouse management
needs and strategies, a practice followed by the wildlife agencies that
have responsibility for management of both species and their habitat.
Taxonomy
Gunnison sage-grouse and greater sage-grouse are members of the
Phasianidae family. For many years, sage-grouse were considered a
single species. Gunnison sage-grouse (Centrocercus minimus) were
identified as a distinct species based on morphological (Hupp and Braun
1991, pp. 257-259; Young et al. 2000, pp. 447-448), genetic (Kahn et
al. 1999, pp. 820-821; Oyler-McCance et al. 1999, pp. 1460-1462), and
behavioral (Barber 1991, pp. 6-9; Young 1994; Young et al. 2000, p.
449-451) differences and geographical isolation (Young et al. 2000, pp.
447-451). Based on these differences, the American Ornithologist's
Union (2000, pp. 849-850) accepted the Gunnison sage-grouse as a
distinct species. The current ranges of the two species do not overlap
(Schroeder et al. 2004, p. 369). Due to the several lines of evidence
separating the two species cited above, we determined that the best
available information indicates that the Gunnison sage-grouse is a
valid taxonomic species and a listable entity under the Act.
Life History Characteristics
Gunnison and greater sage-grouse depend on a variety of shrub-
steppe habitats throughout their life cycle and are considered obligate
users of several species of sagebrush (Patterson 1952, p. 42; Braun et
al. 1976, p. 168; Schroeder et al. 1999, pp. 4-5; Connelly et al.
2000a, pp. 970-972; Connelly et al. 2004, p. 4-1, Miller et al. in
press, p. 10). Dietary requirements of the two species are also
similar, being composed of nearly 100 percent sagebrush in the winter,
and forbs and insects as well as sagebrush in the remainder of the year
(Wallestad et al. 1975, p. 21; Schroeder et al. 1999, p. 5; Young et
al. 2000, p. 452). Gunnison and greater sage-grouse do not possess
muscular gizzards and, therefore, lack the ability to grind and digest
seeds (Leach and Hensley 1954, p. 389).
In addition to serving as a primary year-round food source,
sagebrush also provides cover for nests (Connelly et al. 2000a, pp.
970-971). Thus, sage-grouse distribution is strongly correlated with
the distribution of sagebrush habitats (Schroeder et al. 2004, p. 364).
Connelly et al. (2000a, p. 970-972) segregated habitat requirements
into four seasons: (1) breeding (2) summer - late brood-rearing (3)
fall and (4) winter. Depending on habitat availability and proximity,
some seasonal habitats may be indistinguishable. The Gunnison Sage-
grouse Rangewide Steering Committee (GSRSC) (2005, p. 27-31) segregated
habitat requirements into three seasons: (1) breeding (2) summer-late
fall and (3) winter. For purposes of this finding, the seasons
referenced in GSRSC (2005) are used because that publication deals
specifically with Gunnison sage-grouse.
Sage-grouse exhibit strong site fidelity (loyalty to a particular
area) to seasonal habitats, which includes breeding, nesting, brood
rearing, and wintering areas, even when the area is no longer of value
(Connelly et al. 2004, p. 3-1). Adult sage-grouse rarely switch among
these habitats once they have been selected, limiting their
adaptability to changes. Sage-grouse distribution is associated with
sagebrush (Schroeder et al. 2004 p. 364), although sagebrush is more
widely distributed than sage-grouse because sagebrush does not
[[Page 59806]]
always provide suitable habitat due to fragmentation and degradation
(Schroeder et al. 2004, pp. 369, 372). Very little of the extant
sagebrush in North America is undisturbed, with up to 50 to 60 percent
having altered understories (forb and grass vegetative composition
under the sagebrush) or having been lost to direct conversion (Knick et
al. 2003, p. 612 and references therein). Mapping altered and depleted
understories is challenging, particularly in semi-arid regions, so maps
depicting only sagebrush as a dominant cover type are deceptive in
their reflection of habitat quality and, therefore, use by sage-grouse
(Knick et al. 2003, p. 616 and references therein). As such, variations
in the quality of sagebrush habitats for sage-grouse (from either
abiotic or anthropogenic events) are better reflected by sage-grouse
distribution and densities, rather than by broad geographic scale maps
of the distribution of sagebrush.
Sage-grouse exhibit a polygamous mating system where a male mates
with several females. Males perform courtship displays and defend their
leks (Patterson 1952, p. 83). Lek displaying occurs from mid-March
through late May, depending on elevation (Rogers 1964, p. 21; Young et
al. 2000, p. 448). Numerous researchers have observed that a relatively
small number of dominant males account for the majority of copulations
on each lek (Schroeder et al. 1999, p. 8). However, an average of 45.9
percent (range 14.3 to 54.5 percent) of genetically identified males in
a population fathered offspring in a given year (Bush 2009, p. 106).
This more recent work suggests that males and females likely engage in
off-lek copulations. Males do not incubate eggs or assist in chick
rearing.
Lek sites can be located on areas of bare soil, wind-swept ridges,
exposed knolls, low sagebrush, meadows, and other relatively open sites
with good visibility and low vegetation structure (Connelly et al.
1981, pp. 153-154; Gates 1985, pp. 219-221; Klott and Lindzey 1989, pp.
276-277; Connelly et al. 2004, pp. 3-7 and references therein). In
addition, leks are usually located on flat to gently sloping areas of
less than 15 percent grade (Patterson 1952, p. 83; Giezentanner and
Clark 1974, p. 218; Wallestad 1975, p. 17; Autenrieth 1981, p. 13).
Leks are often surrounded by denser shrub-steppe cover, which is used
for escape, and thermal and feeding cover. Leks can be formed
opportunistically at any appropriate site within or adjacent to nesting
habitat (Connelly et al. 2000a, p. 970). Lek habitat availability is
not considered to be a limiting factor for sage-grouse (Schroeder 1997,
p. 939). However, adult male sage-grouse demonstrate strong yearly
fidelity to lek sites (Patterson 1952, p. 91; Dalke 1963 et al., pp.
817-818), and some Gunnison sage-grouse leks have been used since the
1950s (Rogers 1964, pp. 35-40).
The pre-laying period is from late-March to April. Pre-laying
habitats for sage-grouse need to provide a diversity of vegetation
including forbs that are rich in calcium, phosphorous, and protein to
meet the nutritional needs of females during the egg development period
(Barnett and Crawford 1994, p. 117; Connelly et al. 2000a, p. 970).
During the pre-egg laying period, female sage-grouse select forbs that
generally have higher amounts of calcium and crude protein than
sagebrush (Barnett and Crawford 1994, p. 117).
Nesting occurs from mid-April to June. Average earliest nest
initiation was April 30, and the average latest nest initiation was May
19, in the western portion of the Gunnison Basin (Childers 2009, p. 3).
Radio-tracked Gunnison sage-grouse nest an average of 4.3 kilometers
(km ) (2.7 miles (mi)) from the lek nearest to their capture site, with
almost half nesting within 3 km (2 mi) of their capture site (Young
1994, p. 37). Nest sites are selected independent of lek locations, but
the reverse is not true (Bradbury et al. 1989, p. 22; Wakkinen et al.
1992, p. 382). Thus, leks are indicative of nesting habitat. Eighty-
seven percent of all Gunnison sage-grouse nests were located less than
6 km (4 mi) from the lek of capture (Apa 2004, p. 21). While earlier
studies indicated that most greater sage-grouse hens nest within 3 km
(2 mi) of a lek, more recent research indicated that many hens actually
move much further from leks to nest based on nesting habitat quality
(Connelly et al. 2004, p. 4-4). Female greater sage-grouse have been
documented to travel more than 20 km (13 mi) to their nest site after
mating (Connelly et al. 2000a, p. 970). Female Gunnison sage-grouse
exhibit strong fidelity to nesting locations (Young 1994, p. 42; Lyon
2000, p. 20, Connelly et al. 2004, p. 4-5; Holloran and Anderson 2005,
p. 747). The degree of fidelity to a specific nesting area appears to
diminish if the female's first nest attempt in that area was
unsuccessful (Young 1994, p. 42). However, there is no statistical
indication that movement to new nesting areas results in increased
nesting success (Connelly et al. 2004, p. 3-6; Holloran and Anderson
2005, p. 748).
Gunnison sage-grouse typically select nest sites under sagebrush
cover with some forb and grass cover (Young 1994, p. 38), and
successful nests were found in higher shrub density and greater forb
and grass cover than unsuccessful nests (Young 1994, p. 39). The
understory of productive sage-grouse nesting areas contains native
grasses and forbs, with horizontal and vertical structural diversity
that provides an insect prey base, herbaceous forage for pre-laying and
nesting hens, and cover for the hen while she is incubating (Schroeder
et al. 1999, p. 11; Connelly et al. 2000a, p. 971; Connelly et al.
2004, pp. 4-5-4-8). Shrub canopy and grass cover provide concealment
for sage-grouse nests and young, and are critical for reproductive
success (Barnett and Crawford 1994, pp. 116-117; Gregg et al. 1994, pp.
164-165; DeLong et al. 1995, pp. 90-91; Connelly et al. 2004, p. 4-4).
Few herbaceous plants are growing in April when nesting begins, so
residual herbaceous cover from the previous growing season is critical
for nest concealment in most areas (Connelly et al. 2000a, p. 977).
Nesting success for Gunnison sage-grouse is highest in areas where
forb and grass covers are found below a sagebrush canopy cover of 15 to
30 percent (Young et al. 2000, p. 451). These numbers are comparable to
those reported for the greater sage-grouse (Connelly et al. 2000a, p.
971). Nest success for greater sage-grouse is greatest where grass
cover is present (Connelly et al. 2000a, p. 971). Because of the
similarities between these two species, we believe that increased nest
success in areas of forb and grass cover below the appropriate
sagebrush canopy cover is likely the case for Gunnison sage-grouse as
well.
Mean clutch size for Gunnison sage-grouse is 6.8 0.7
eggs (Young 1994, p. 37). The mean clutch size for Gunnison sage-grouse
in the Gunnison Basin was 6.3, with 94 percent of eggs in successful
nests hatching (Childers 2009, p. 3). Despite average clutch sizes of 7
eggs (Connelly et al. in press, p. 15), little evidence exists that
populations of sage-grouse produce large annual surpluses (Connelly et
al. in press, p. 15, 24). The inability of sage-grouse to produce large
annual surpluses limits their ability to respond under favorable
environmental conditions to make up for population declines. Re-nesting
rates following the loss of the original nest appear very low in
Gunnison sage-grouse, with one study reporting re-nesting rates of 4.8
percent (Young 1994, p. 37). Only one instance of re-nesting was
observed over a 5-year period during which a total of 91 nesting
Gunnison sage-grouse hens were monitored (Childers 2009, p. 3).
Most sage-grouse eggs hatch in June, with a peak between June 10
and June
[[Page 59807]]
20 (GSRSC, 2005, p. 24). Chicks are precocial (mobile upon hatching)
and leave the nest with the hen shortly after hatching. Forbs and
insects are essential nutritional components for sage-grouse chicks
(Klebenow and Gray 1968, pp. 81-83; Peterson 1970, pp. 149-151; Johnson
and Boyce 1991, p. 90; Connelly et al. 2004, p. 3-3). Therefore, early
brood-rearing habitat for females with chicks must provide adequate
cover adjacent to areas rich in forbs and insects to assure chick
survival during this period (Connelly et al. 2000, p. 971; Connelly et
al. 2004, p. 4-11). Gunnison sage-grouse chick dietary requirements of
insects and forbs also are expected to be similar to greater sage-
grouse and other grouse species (Apa 2005, pers. comm.).
The availability of food and cover are key factors that affect
chick and juvenile survival. During the first 3 weeks after hatching,
insects are the primary food of chicks (Patterson 1952, p. 201;
Klebenow and Gray 1968, p. 81; Peterson 1970, pp. 150-151; Johnson and
Boyce 1990, pp. 90-91; Johnson and Boyce 1991, p. 92; Drut et al.
1994b, p. 93; Pyle and Crawford 1996, p. 320; Fischer et al. 1996a, p.
194). Diets of 4- to 8-week-old greater sage-grouse chicks were found
to have more plant material as the chicks matured (Peterson 1970, p.
151). Succulent forbs are predominant in the diet until chicks exceed 3
months of age, at which time sagebrush becomes a major dietary
component (Klebenow 1969, pp. 665-656; Connelly and Markham 1983, pp.
171-173; Fischer et al. 1996b, p. 871; Schroeder et al. 1999, p. 5).
Early brood-rearing habitat is found close to nest sites (Connelly
et al. 2000a, p. 971), although individual females with broods may move
large distances (Connelly 1982, as cited in Connelly et al. 2000a, p.
971). Young (1994, pp. 41-42) found that Gunnison sage-grouse with
broods used areas with lower slopes than nesting areas, high grass and
forb cover, and relatively low sagebrush cover and density. Broods
frequently used the edges of hay meadows, but were often flushed from
areas found in interfaces of wet meadows and habitats providing more
cover, such as sagebrush or willow-alder (Salix-Alnus).
By late summer and into the early fall, individuals become more
social, and flocks are more concentrated (Patterson 1952, p. 187).
Intermixing of broods and flocks of adult birds is common, and the
birds move from riparian areas to sagebrush-dominated landscapes that
continue to provide green forbs. During this period, Gunnison sage-
grouse can be observed in atypical habitat such as agricultural fields
(Commons 1997, pp. 79-81). However, broods in the Gunnison Basin
typically do not use hay meadows further away than 50 meters (m) (165
feet (ft)) of the edge of sagebrush stands (Colorado Sage Grouse
Working Group (CSGWG) 1997, p. 13).
As fall approaches, sage-grouse move from riparian to upland areas
and start to shift to a winter diet (GSRSC 2005, p. 25). Movements to
winter ranges are slow and meandering (Connelly et al. 1988, p. 119).
The extent of movement varies with severity of winter weather,
topography, and vegetation cover. Sage-grouse may travel short
distances or many miles between seasonal ranges. In response to severe
winters, Gunnison sage-grouse move as far as 27 km (17 mi) (Root 2002,
p. 14). Flock size in winter is variable (15 to 100+), and flocks
frequently consist of a single sex (Beck 1977, p. 21).
From late autumn through early spring, greater and Gunnison sage-
grouse diet is almost exclusively sagebrush (Rasmussen and Griner 1938,
p. 855; Batterson and Morse 1948, p. 20; Patterson 1952, pp. 197-198;
Wallestad et al. 1975, pp. 628-629; Young et al. 2000, p. 452). Many
species of sagebrush can be consumed (Remington and Braun 1985, pp.
1056-1057; Welch et al. 1988, p. 276, 1991; Myers 1992, p. 55).
Characteristics of sage-grouse winter habitats are also similar through
the range of both species (Connelly et al. 2000a, p. 972). In winter,
Gunnison sage-grouse are restricted to areas of 15 to 30 percent
sagebrush cover, similar to the greater sage-grouse (Connelly et al.
2000a, p. 972; Young et al. 2000, p. 451). However, they may also use
areas with more deciduous shrubs during the winter (Young et al. 2000,
p. 451).
Sagebrush stand selection in winter is influenced by snow depth
(Patterson 1952, pp. 188-189; Connelly 1982 as cited in Connelly et al.
2000a, p. 980) and in some areas, topography (Beck 1977, p. 22;
Crawford et al. 2004, p. 5). Winter areas are typically characterized
by canopy cover greater than 25 percent and sagebrush greater than 30
to 41 cm (12 to 16 in) tall (Shoenberg 1982, p. 40) associated with
drainages, ridges, or southwest aspects with slopes less than 15
percent (Beck 1977, p. 22). Lower flat areas and shorter sagebrush
along ridge tops provide roosting areas. In extreme winter conditions,
greater sage-grouse will spend nights and portions of the day burrowed
into ``snow burrows'' (Back et al. 1987, p. 488).
Hupp and Braun (1989, p. 825) found that most Gunnison sage-grouse
feeding activity in the winter occurred in drainages and on slopes with
south or west aspects in the Gunnison Basin. During a severe winter in
the Gunnison Basin in 1984, less than 10 percent of the sagebrush was
exposed above the snow and available to sage-grouse (Hupp, 1987, pp.
45-46). In these conditions, the tall and vigorous sagebrush typical in
drainages was an especially important food source.
Sage-grouse typically live between 3 and 6 years, but individuals
up to 9 years of age have been recorded in the wild (Connelly et al.
2004, p. 3-12). Adult female Gunnison sage-grouse apparent survival
rates from April through September averaged 57 percent, and adult male
survival averaged 45 percent (Childers 2009, p. 2). From October
through March, adult female Gunnison sage-grouse apparent survival
rates averaged 79 percent, and adult male survival averaged 96 percent
(Childers 2009, p.2). In one study, Gunnison sage-grouse survival from
April 2002 through March 2003 was 48 ( 7) percent for males
and 57 ( 7) percent for females (Apa 2004, p. 22).
Preliminary results from the Gunnison and San Miguel populations
indicate potential important temporal and spatial variation in
demographic parameters, with apparent annual adult survival rates
ranging from approximately 65 to 80 percent (CDOW 2009a, p. 8).
Gunnison sage-grouse female survival in small isolated populations was
52 ( 8) percent, compared to 71 ( 11) percent
survival in the Gunnison Basin, the only population with greater than
500 individuals (Apa 2004, p. 22). Higher adult survival has been
observed in a lower elevation and warmer area (Dry Creek Basin of the
San Miguel population - 90 percent) than in a higher elevation and
colder, snowier, area (Miramonte portion of the San Miguel population -
65 percent) (CDOW 2009a, p.8). Other factors affecting survival rates
include climatic differences between years and age (Zablan 1993, pp. 5-
6).
Apparent chick survival from hatch to the beginning of fall (30
September) averaged 7 percent over a 5-year period in the western
portion of the Gunnison Basin (Childers 2009, pp. 4-6). Apparent chick
survival to 90 days of age has ranged from approximately 15 to 30
percent in the Gunnison Basin, with no juvenile recruitment observed
over several years in the San Miguel population (CDOW 2009a, p. 8).
Based on a review of many field studies, juvenile survival rates range
from 7 to 60 percent (Connelly et al. 2004, p. 3-12). The variation in
juvenile survival rates may be associated with sex, weather, harvest
rates (no harvesting of Gunnison sage-grouse is currently permitted),
age of brood female (broods with adult females have higher
[[Page 59808]]
survival), and with habitat quality (rates decrease in poor habitats)
(Schroeder et al. 1999, p. 14; Connelly et al., in press, p. 20).
Greater sage-grouse require large, interconnected expanses of
sagebrush with healthy, native understories (Patterson 1952, p. 9;
Knick et al. 2003, p. 623; Connelly et al. 2004, pp. 4-15; Connelly et
al. in press, p. 10; Pyke in press, p. 7; Wisdom et al. in press, p.
4). However, little information is available regarding minimum
sagebrush patch sizes required to support populations of greater or
Gunnison sage-grouse. Gunnison sage-grouse have not been observed to
undertake the large seasonal and annual movements observed in greater
sage-grouse. However, movements of up to 24 km (15 mi) have been
observed in individual Gunnison sage-grouse in the Gunnison Basin
population only (Phillips 2010, pers. comm.).
Sage-grouse typically occupy large expanses of sagebrush-dominated
habitats composed of a diversity of sagebrush species and subspecies.
Use of other habitats intermixed with sagebrush, such as riparian
meadows, agricultural lands, steppe dominated by native grasses and
forbs, scrub willow (Salix spp.), and sagebrush habitats with some
conifer or quaking aspen (Populus tremuloides), is not uncommon
(Connelly et al 2004, p. 4-18 and references therein). Sage-grouse have
been observed using human-altered habitats throughout their range.
However, the use of non-sagebrush habitats by sage-grouse is
dependent on the presence of sagebrush habitats in close proximity
(Connelly et a.lal 2004, p. 4-18 and references therein).
Historic Range and Distribution of Gunnison Sage-grouse
Based on historical records, museum specimens, and potential
habitat distribution, Gunnison sage-grouse historically occurred in
southwestern Colorado, northwestern New Mexico, northeastern Arizona,
and southeastern Utah (Schroeder et al. 2004, pp. 370-371). Accounts of
Gunnison sage-grouse in Kansas and Oklahoma, as suggested by Young et
al. (2000, pp. 446-447), are not supported with museum specimens, and
Schroeder et al. (2004, p. 371) found inconsistencies with the
historical records and the sagebrush habitat currently available in
those areas. Applegate (2001, p. 241) found that none of the sagebrush
species closely associated with sage-grouse occurred in Kansas. He
attributed historical, anecdotal reports as mistaken locations or
misidentification of lesser prairie chickens. For these reasons,
southwestern Kansas and western Oklahoma are not considered within the
historic range of Gunnison sage-grouse (Schroeder et al. 2004, p. 371).
The GSRSC (2005) modified the historic range from Schroeder et al.
(2004), based on more complete information on historic and current
habitat and the distribution of the species (GSRSC 2005, pp. 34-35).
Based on this information, the maximum Gunnison sage-grouse historical
(presettlement) range is estimated to have been 55,350 square
kilometers (km\2\) (21,370 square miles (mi\2\)) (GSRSC 2005, p. 32).
To be clear, only a portion of the historical range would have been
occupied at any one time, while all of the current range is considered
occupied. Also, we do not know what portion of the historical range was
simultaneously occupied, or what the total population was.
Much of what was once Gunnison sage-grouse sagebrush habitat was
already lost prior to 1958. A qualitative decrease in sagebrush was
attributed to overgrazing from the 1870s until about 1934 (Rogers 1964,
p. 13). Additional adverse effects occurred as a result of newer range
management techniques implemented to support livestock by the Bureau of
Land Management (BLM), Soil Conservation Service, and U.S. Forest
Service (USFS) (Rogers 1964, p. 13). In the 1950s, large areas of
sagebrush within the range of Gunnison sage-grouse were eradicated by
herbicide spraying or burning (Rogers 1964, pp. 12-13, 22-23, 26).
About 155,673 hectares (ha) (384,676 ac) of sagebrush habitat was
lost from 1958 to 1993 within southwestern Colorado (Oyler-McCance et
al. 2001, p. 327). Sagebrush loss was lower in the Gunnison Basin (11
percent) compared to all other areas in southwestern Colorado (28
percent) (Oyler-McCance et al. 2001, p. 328). Considerable
fragmentation of sagebrush vegetation was also quantitatively
documented during that same time period (Oyler-McCance et al. 2001, p.
329). Sage-grouse habitat in southwestern Colorado (the majority of the
range of Gunnison sage-grouse) has been more severely impacted than
sagebrush habitat elsewhere in Colorado.
The Colorado River Storage Project (CRSP) resulted in construction
of three reservoirs within the Gunnison Basin in the mid-late 1960s
(Blue Mesa and Morrow) and mid-1970s (Crystal). Several projects
associated with CRSP were constructed in this same general timeframe to
provide additional water storage and resulted in the loss of an
unquantified, but likely small, amount of sagebrush habitat. These
projects provide water storage and, to a certain extent, facilitate
agricultural activities that maintain the fragmentation and habitat
lost historically throughout the range of Gunnison sage-grouse.
In summary, a substantial amount of sagebrush habitat within the
range of the Gunnison sage-grouse had been lost prior to 1960. The
majority of the remaining habitat is highly fragmented, although to a
lesser extent in the Gunnison Basin than in the remainder of the
species habitat.
Current Distribution and Population Estimates
The historic and current geographic ranges of Gunnison's and
greater sage-grouse were quantitatively analyzed to determine the
species' response to habitat loss and detrimental land uses (Wisdom et
al., in press, 2009, entire). A broad spectrum of biotic, abiotic, and
anthropogenic conditions were found to be significantly different
between extirpated and occupied ranges (Wisdom et al., in press, 2009,
p. 1.). Sagebrush area is one of the best landscape predictors of sage-
grouse persistence (Wisdom et al., in press, 2009, p. 17 and references
therein). Because of the loss and fragmentation of habitat within its
range, no expansive, contiguous areas that could be considered
strongholds (areas of occupied range where the risk of extirpation
appears low) are evident for Gunnison sage-grouse (Wisdom et al., in
press, 2009, p. 24). We do not know the minimum amount of sagebrush
habitat needed by Gunnison sage-grouse to ensure long-term persistence.
However, based on Wisdom et al., in press, we do know that landscapes
containing large and contiguous sagebrush patches and sagebrush patches
in close proximity increase the likelihood of sage-grouse persistence.
Gunnison sage-grouse currently occur in seven widely scattered and
isolated populations in Colorado and Utah, occu2pying 3,795 km\2\
(1,511mi\2\) (GSRSC 2005, pp. 36-37; CDOW 2009b, p. 1). The seven
populations are Gunnison Basin, San Miguel Basin, Monticello-Dove
Creek, Pinon Mesa, Crawford, Cerro Summit-Cimarron-Sims Mesa, and
Poncha Pass (Figure 1). A comparative summary of the land ownership and
recent population estimates among these seven populations is presented
in Table 1 and Table 2, respectively. Population trends over the last
nine years indicate that six of the populations are in decline. The
Gunnison Basin population, while showing variation over the years, has
been relatively stable through the period (CDOW 2009a p. 2). Six of the
[[Page 59809]]
populations are very small and fragmented (all with less than 40,500 ha
(100,000 acres) of habitat likely used by grouse and less than 50 males
counted on leks) (CDOW 2009a, p. 5). The San Miguel population, the
second largest, comprises six fragmented subpopulations.
Figure 1. Locations of Current Gunnison Sage-grouse Populations.
[GRAPHIC] [TIFF OMITTED] TP28SE10.000
Table 1. Percent surface ownership of total Gunnison sage-grouse occupied\a\ habitat (from GSRSC\b\ 2005, pp. D-3-D-6; CDOW\c\ 2009b, p. 1)
--------------------------------------------------------------------------------------------------------------------------------------------------------
Gunnison Sage-grouse Occupied Habitat Management and Ownership
-----------------------------------------------------------------------------------------------------------------------------------------------
Population hectares acres BLM\d\ NPS\e\ USFS\f\ CDOW CO State State of Private
----------------------------------------------------------------------------------------------------------------- Land UT ----------
Board ----------
% % % % ---------- %
% %
-----------------------------------------------------------------------------------------------------------------------------------------------
Gunnison Basin 239,953 592,936 51 2 14 3 <1 0 29
--------------------------------------------------------------------------------------------------------------------------------------------------------
San Miguel Basin 41,022 101,368 36\g\ 0 1 11 3\g\ 0 49\g\
--------------------------------------------------------------------------------------------------------------------------------------------------------
Monticello-Dove Creek (Combined) 45,275 111,877 7 0 0 3 0 <1 90
--------------------------------------------------------------------------------------------------------------------------------------------------------
Dove Creek 16,706 41,282 11 0 0 8 0 0 81
--------------------------------------------------------------------------------------------------------------------------------------------------------
Monticello 28,569 70,595 4 0 0 0 0 1 95
--------------------------------------------------------------------------------------------------------------------------------------------------------
Pi[ntilde]on Mesa 15,744 38,904 28 0 2 19 0 0 51
--------------------------------------------------------------------------------------------------------------------------------------------------------
Cerro Summit-Cimarron-Sims Mesa 15,039 37,161 13 <1 0 11 0 0 76
--------------------------------------------------------------------------------------------------------------------------------------------------------
Crawford 14,170 35,015 63 12 0 2 0 0 23
--------------------------------------------------------------------------------------------------------------------------------------------------------
[[Page 59810]]
Poncha Pass 8,262 20,415 48 0 26 0 2 0 23
--------------------------------------------------------------------------------------------------------------------------------------------------------
Rangewide 379,464 937,676 42 2 10 5 <1 <1 41
--------------------------------------------------------------------------------------------------------------------------------------------------------
\a\Occupied Gunnison sage-grouse habitat is defined as areas of suitable habitat known to be used by Gunnison sage-grouse within the last 10 years from
the date of mapping, and areas of suitable habitat contiguous with areas of known use, which have no barriers to grouse movement from known use areas
(GSRSC 2005, p. 54).
\b\Gunnison Sage-grouse Rangewide Steering Committee
\c\Colorado Division of Wildlife
\d\Bureau of Land Management
\e\National Park Service
\f\United States Forest Service
\g\Estimates reported in San Miguel Basin Gunnison Sage-grouse Conservation Plan (2009 p. 28) vary by up to 2 percent in these categories from those
reported here. We consider these differences insignificant.
Table 2. Gunnison Sage-grouse population estimates by year derived from the formula presented in the Gunnison sage-grouse Rangewide Conservation Plan
(GSRSC\a\ 2005, pp. 44-45) applied to high male counts on leks (CDOW\b\ 2009a, p. 2).
--------------------------------------------------------------------------------------------------------------------------------------------------------
Estimated Population
-----------------------------------------------------------------------------------------------------------------
Year
-----------------------------------------------------------------------------------------------------------------
2001 2002 2003 2004 2005 2006 2007 2008 2009 2010
--------------------------------------------------------------------------------------------------------------------------------------------------------
Gunnison Basin 3,493 3,027 2,453 2,443 4,700 5,205 4,616 3,669 3,817 3,655
--------------------------------------------------------------------------------------------------------------------------------------------------------
San Miguel Basin 392 383 250 255 334 378 324 216 162 123
--------------------------------------------------------------------------------------------------------------------------------------------------------
Monticello-Dove Creek (Combined) 363 270 186 162 196 191 245 245 191 n/a\c\
--------------------------------------------------------------------------------------------------------------------------------------------------------
Monticello 231 172 147 152 162 118 216 216 182 n/a\c\
--------------------------------------------------------------------------------------------------------------------------------------------------------
Dove Creek 132 98 39 10 34 74 29 29 10 44
--------------------------------------------------------------------------------------------------------------------------------------------------------
Pi[ntilde]on Mesa 152 132 123 142 167 152 123 108 78 74
--------------------------------------------------------------------------------------------------------------------------------------------------------
Cerro Summit-Cimarron-Sims Mesa 59 39 29 39 25 49 34 10 39 5
--------------------------------------------------------------------------------------------------------------------------------------------------------
Crawford 137 206 118 128 191 201 113 103 78 20
--------------------------------------------------------------------------------------------------------------------------------------------------------
Poncha Pass 25 44 34 39 44 44 25 25 20 15
--------------------------------------------------------------------------------------------------------------------------------------------------------
Totals 4,621 4,101 3,194 3,208 5,656 6,220 5,480 4,376 4,386 n/a\c\
--------------------------------------------------------------------------------------------------------------------------------------------------------
\a\Gunnison Sage-grouse Rangewide Steering Committee
\b\Colorado Division of Wildlife
\c\2010 lek count data for the Monticello group was not available at the time of publication
Gunnison Basin Population - The Gunnison Basin is an intermontane
basin that includes parts of Gunnison and Saguache Counties, Colorado.
The current Gunnison Basin population is distributed across
approximately 240,000 ha (593,000 ac), roughly centered on the town of
Gunnison. Elevations in the area range from 2,300 to 2,900 m (7,500 to
9,500 ft). Approximately 70 percent of the land area is managed by
Federal agencies (67 percent) and CDOW (3 percent), and the remaining
30 percent comprises primarily private lands. Big sagebrush (Artemesia
tridentata) dominates the upland vegetation and has a highly variable
growth form depending on local site conditions. In 2009, 83 leks were
surveyed for breeding activity in the Gunnison Basin, and 42 of these
leks were active (at least two males in attendance during at least two
of four 10-day count periods), 6 inactive
[[Page 59811]]
(inactive for at least 5 consecutive years), 9 historic (inactive for
at least 10 consecutive years), and 26 were of unknown status
(variability in counts resulted in lek not meeting requirements for
active, inactive, or historic) (CDOW 2009d, pp. 28-30). Approximately
45 percent of leks in the Gunnison Basin occur on private land and 55
percent on public land, primarily BLM (GSRSC 2005, p. 75). The 2010
population estimate for the Gunnison Basin was 3,655 (CDOW 2010a, p.
2). Rogers (1964, p. 20) stated that Gunnison County was one of five
counties containing the majority of sage-grouse in Colorado in 1961.
The vast majority (87 percent) of Gunnison sage-grouse are now found
only in the Gunnison Basin population.
San Miguel Basin Population - The San Miguel Basin population is in
Montrose and San Miguel Counties in Colorado, and is composed of six
small subpopulations using different areas--(Dry Creek Basin, Hamilton
Mesa, Miramonte Reservoir, Gurley Reservoir, Beaver Mesa, and Iron
Springs) occupying a total of approximately 41,000 ha (101,000 ac).
Some of these six areas are used year-round by sage-grouse, and others
are used seasonally. The overall acreage figure for this population is
heavily skewed by the large percentage (approximately 62 percent) of
land in the Dry Creek Basin (San Miguel Basin Gunnison Sage-grouse
Working Group 2009, p. 28). The Dry Creek Basin area contains some of
the poorest habitat and smallest grouse populations in the San Miguel
population (San Miguel Basin Gunnison sage-grouse Conservation Plan
2009, pp. 28, 36). Gunnison sage-grouse in the San Miguel Basin move
widely between these areas (Apa 2004, p. 29; Stiver and Gibson 2005, p.
12). The area encompassed by this population is believed to have once
served as critical migration corridors between populations to the north
(Cerro Summit-Cimarron-Sims Mesa) and to the south (Monticello-Dove
Creek) (San Miguel Basin Gunnison Sage-grouse Working Group 2009, p.
9).
Sagebrush habitat in the Dry Creek Basin area is patchily
distributed, and the understory is either lacking in grass and forb
diversity or nonexistent. Where irrigation is possible, private lands
in the southeast portion of Dry Creek Basin are cultivated. Sagebrush
habitat on private land has been heavily thinned or removed entirely
(GSRSC 2005, p. 96). Gunnison sage-grouse use the Hamilton Mesa area
(1,940 ha (4,800 ac)) in the summer, but use of Hamilton Mesa during
other seasons is unknown. Gunnison sage-grouse occupy approximately
4,700 ha (11,600 ac) around Miramonte Reservoir (GSRSC 2005, p. 96).
Sagebrush stands there are generally contiguous with a mixed grass and
forb understory. Occupied habitat at the Gurley Reservoir area (3,305
ha (7,500 ac)) is heavily fragmented by urban development, and the
understory is a mixed grass and forb community. Farming attempts in the
early 20th century led to the removal of much of the sagebrush,
although agricultural activities are now restricted primarily to the
seasonally irrigated crops (hay meadows), and sagebrush has
reestablished in most of the failed pastures. However, grazing pressure
and competition from introduced grasses have kept the overall sagebrush
representation low (GSRSC 2005, pp. 96-97). Sagebrush stands in the
Iron Springs and Beaver Mesa areas (2,590 ha and 3,560 ha (6,400 ac and
8,800 ac respectively)) are contiguous with a mixed grass understory.
The Beaver Mesa area has numerous scattered patches of oakbrush
(Quercus gambelii). Rogers (1964, p. 9) reported that all big
sagebrush-dominated habitats in San Miguel and Montrose Counties were
historically used by Gunnison sage-grouse.
The 2010 population estimate for the entire San Miguel Basin was
123 individuals on nine leks (CDOW 20010, p. 3). With the exception of
2007, CDOW has been translocating Gunnison sage-grouse from the
Gunnison Basin to Dry Creek Basin on a yearly basis since the spring of
2006 (CDOW 2009a, p. 133). In the spring of 2006, six individuals were
released near the Desert Lek. An additional two individuals were
released in the fall. Nine individuals were translocated in the spring
of 2008. An additional 30 individuals were translocated in the fall of
2009. A 40 to 50 percent mortality rate has been observed within the
first year after release, compared to an average annual mortality rate
of approximately 20 percent for radiomarked adult sage-grouse (CDOWa
2009, p. 9).
Monticello-Dove Creek Population - This population is divided into
two disjunct subpopulations of Gunnison sage-grouse. Currently, the
largest group is near the town of Monticello, in San Juan County, Utah.
Gunnison sage-grouse in this subpopulation inhabit a broad plateau on
the northeast side of the Abajo Mountains, with fragmented patches of
sagebrush interspersed with large grass pastures and agricultural
fields. The Utah Division of Wildlife Resources (UDWR) estimated
population numbers between 583 and 1,050 individuals in 1972 and
between 178 and 308 individuals in 2002 (UDWR 2009, 29.21 p. 1). The
UDWR estimates that Gunnison sage-grouse currently occupy about 24,000
ha (60,000 ac) in the Monticello area. The 2009 population estimate for
Monticello was 182 individuals with three active and one inactive leks
(UDWR 2009, p. 5).
The Dove Creek subpoulation is located primarily in western Dolores
County, Colorado, north and west of Dove Creek, although a small
portion of occupied habitat extends north into San Miguel County.
Habitat north of Dove Creek is characterized as mountain shrub habitat,
dominated by oakbrush interspersed with sagebrush. The area west of
Dove Creek is dominated by sagebrush, but the habitat is highly
fragmented. Lek counts in the Dove Creek area were over 50 males in
1999, suggesting a population of about 245 birds, but declined to 2
males in 2009 (CDOW 2009a, p. 71), suggesting a population of 10 birds.
A new lek was found in 2010, and the 2010 population estimate was 44
individuals on 2 leks (CDOW 2010, p. 1). Low sagebrush canopy cover, as
well as low grass height, exacerbated by drought, may have led to nest
failure and subsequent population declines (Connelly et al. 2000a, p.
974; Apa 2004, p. 30). Rogers (1964, p. 9) reported that all sagebrush-
dominated habitats in Dolores and Montezuma Counties within Gunnison
sage-grouse range in Colorado were historically used by Gunnison sage-
grouse.
Pinon Mesa Population - The Pinon Mesa population occurs on the
northwest end of the Uncompahgre Plateau in Mesa County, about 35 km
(22 mi) southwest of Grand Junction, Colorado. The 2010 population
estimate for Pinon Mesa was 74 (CDOW 2010, p. 2). Of the ten known
leks, only four were active in 2009 (CDOW, 2009a, p. 3). The Pinon Mesa
area may have additional leks, but the high percentage of private land,
a lack of roads, and heavy snow cover during spring make locating
additional leks difficult. Gunnison sage-grouse likely occurred
historically in all suitable sagebrush habitat in the Pinon Mesa area,
including the Dominguez Canyon area of the Uncompaghre Plateau,
southeast of Pinon Mesa proper (Rogers 1964, p. 114). Their current
distribution has been substantially reduced from historic levels to
15,744 ha (38,904 ac) (GSRSC 2005, p. 87).
Crawford Population - The Crawford population of Gunnison sage-
grouse is in Montrose County, Colorado, about 13 km (8 mi) southwest of
the town of Crawford and north of the Gunnison River. Basin big
sagebrush (Artemisia tridentata tridentata) and black
[[Page 59812]]
sagebrush (A. nova) dominate the mid-elevation uplands (GSRSC 2005, p.
62). The 2010 population estimate for Crawford was 20 individuals (CDOW
2010, p. 1) in 14,170 ha (35,015 ac) of occupied habitat. Four active
leks are currently in the Crawford population on BLM lands in sagebrush
habitat adjacent to an 11-km (7-mi) stretch of road. This area
represents the largest contiguous sagebrush-dominated habitat within
the Crawford boundary (GSRSC 2005, p. 64).
Cerro Summit-Cimarron-Sims Mesa Population - This population is
divided into two geographically separated subpopulations, both in
Montrose County, Colorado. The Cerro Summit-Cimarron subpopulation is
centered about 24 km (15 mi) east of Montrose. The habitat consists of
15,039 ha (37,161 ac) of patches of sagebrush habitat fragmented by
oakbrush and irrigated pastures. Five leks are currently known in the
Cerro Summit-Cimarron group, but only one individual was observed on
one lek in 2010 resulting in a population estimate of 5 individuals for
the population (CDOW 2010, p. 1). Rogers (1964, p. 115) noted a small
population of sage-grouse in the Cimarron River drainage, but did not
report population numbers. He noted that lek counts at Cerro Summit in
1959 listed four individuals.
The Sims Mesa area, about 11 km (7 mi) south of Montrose, consists
of small patches of sagebrush that are heavily fragmented by pinyon-
juniper, residential and recreational development, and agriculture. The
one known lek in Sims Mesa has lacked Gunnison sage-grouse attendance
for the last six years, which indicates this population is likely
extirpated (CDOW 2009a, p. 43). In 2000, the CDOW translocated six
Gunnison sage-grouse from the Gunnison Basin to Sims Mesa (Nehring and
Apa 2000, p. 12). Rogers (1964, p. 95) recorded eight males in a lek
count at Sims Mesa in 1960. We do not know if sage-grouse move between
the Cerro Summit-Cimarron and Sims Mesa subpopulations.
Poncha Pass Population - The Poncha Pass Gunnison sage-grouse
population is located in Saguache County, approximately 16 km (10 mi)
northwest of Villa Grove, Colorado. This population was established
through the reintroduction of 30 birds from the Gunnison Basin in 1971
and 1972 during efforts to reintroduce the species to the San Luis
Valley (GSRSC 2005, p. 94). The known population distribution is in
8,262 ha (20,415 ac) of sagebrush habitat from the summit of Poncha
Pass extending south for about 13 km (8 mi) on either side of U.S.
Highway 285. Sagebrush in this area is continuous with little
fragmentation; sagebrush habitat quality throughout the area is
adequate to support the species (Nehring and Apa 2000 p. 25). San Luis
Creek runs through the area, providing a year-round water source and
lush, wet meadow riparian habitat for brood-rearing.
A high male count of 3 males was made in 2010 (CDOW 2009a, p. 121),
resulting in an estimated population size of 15 for the Poncha Pass
population (CDOW 2010, p. 3). The only current lek is located on BLM-
administered land. In 1992, a CDOW effort to simplify hunting
restrictions inadvertently opened the Poncha Pass area to sage-grouse
hunting, and at least 30 grouse were harvested from this population.
Due to declining population numbers since the 1992 hunt, CDOW
translocated 24 additional birds from the Gunnison Basin (Nehring and
Apa 2000, p. 11). In 2001 and 2002, an additional 20 and 7 birds,
respectively, were moved to Poncha Pass by the CDOW (GSRSC 2005, p.
94). Translocated females have bred successfully (Apa 2004, pers.
comm.), and display activity resumed on the historic lek in spring
2001.
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: (1) The present
or threatened destruction, modification, or curtailment of its habitat
or range; (2) overutilization for commercial, recreational, scientific,
or educational purposes; (3) disease or predation; (4) the inadequacy
of existing regulatory mechanisms; or (5) other natural or manmade
factors affecting its continued existence. In making this finding,
information pertaining to the Gunnison sage-grouse, in relation to the
five factors provided in section 4(a)(1) of the Act, is discussed
below.
In considering what factors might constitute threats to a species,
we must look beyond the exposure of the species to a factor to evaluate
whether the species may respond to the factor in a way that causes
actual impacts to the species. If there is exposure to a factor and the
species responds negatively, the factor may be a threat and we attempt
to determine how significant a threat it is. The threat is significant
if it drives, or contributes to, the risk of extinction of the species
such that the species warrants listing as endangered or threatened as
those terms are defined in the Act.
The Gunnison Basin contains 87 percent of the current rangewide
Gunnison sage-grouse population and 62 percent of the area occupied by
the species. The remaining six populations cumulatively and
individually have substantially smaller population sizes and occupy
substantially less habitat than the Gunnison Basin population (see
Table 2).
A. The Present or Threatened Destruction, Modification, or Curtailment
of Its Habitat or Range
Sagebrush habitats within the range of Gunnison sage-grouse are
becoming increasingly fragmented as a result of various changes in land
uses and the expansion in the density and distribution of invasive
plant species (Oyler-McCance et al. 2001, pp. 329-330; Schroeder et al.
2004, p. 372). Habitat fragmentation is the separation or splitting
apart of previously contiguous, functional habitat components of a
species. Fragmentation can result from direct habitat losses that leave
the remaining habitat in non-contiguous patches, or from alteration of
habitat areas that render the altered patches unusable to a species
(i.e., functional habitat loss). Functional habitat losses include
disturbances that change a habitat's successional state or remove one
or more habitat functions; physical barriers that preclude use of
otherwise suitable areas; or activities that prevent animals from using
suitable habitat patches due to behavioral avoidance.
A variety of human developments including roads, energy
development, and other factors that cause habitat fragmentation have
contributed to or been associated with Gunnison and greater sage-grouse
extirpation (Wisdom et al. in press, p. 18). Based on a quantitative
analysis of environmental factors most closely associated with
extirpation, no strongholds (areas where the risk of Gunnison sage-
grouse extirpation is low) exist (Wisdom et al. in press, p. 26).
Estimating the impact of habitat fragmentation on sage-grouse is
complicated by time lags in response to habitat changes (Garton et al.,
in press, p. 71), particularly since these relatively long-lived birds
will continue to return to altered breeding areas (leks, nesting areas,
and early brood-rearing areas) due to strong site fidelity despite
nesting or productivity failures (Rogers 1964, pp. 35-40; Wiens and
Rotenberry 1985, p. 666; Young 1994, p. 42; Lyon
[[Page 59813]]
2000, p. 20, Connelly et al. 2004, p. 45; Holloran and Anderson 2005,
p. 747).
Habitat fragmentation can have an adverse effect on Gunnison sage-
grouse populations. Many of the factors that result in fragmentation
may be exacerbated by the effects of climate change, which may
influence long-term habitat and population trends. The following
sections examine factors that can contribute to habitat fragmentation
to determ