Endangered and Threatened Wildlife and Plants; Final Listing Determination for the Gunnison Sage-Grouse as Threatened or Endangered, 19954-19982 [06-3619]
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Federal Register / Vol. 71, No. 74 / Tuesday, April 18, 2006 / Rules and Regulations
DEPARTMENT OF THE INTERIOR
Fish and Wildlife Service
50 CFR Part 17
Endangered and Threatened Wildlife
and Plants; Final Listing Determination
for the Gunnison Sage-Grouse as
Threatened or Endangered
Fish and Wildlife Service,
Interior.
ACTION: Final listing determination.
AGENCY:
SUMMARY: We, the U.S. Fish and
Wildlife Service (Service), announce a
final listing determination for 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
listing is not warranted. Thus, we no
longer consider the species to be a
candidate for listing. We ask the public
to submit to us any new information
that becomes available concerning the
status of or threats to the species. This
information will help us monitor and
encourage the conservation of this
species.
The determination announced in
this document was made on April 11,
2006. Although further listing action
will not result from this determination,
we request that you submit new
information concerning the status of or
threats to this species whenever it
becomes available.
ADDRESSES: Comments and materials
received, as well as supporting
documentation used in the preparation
of this final listing determination, will
be available for inspection, by
appointment, during normal business
hours at the Western Colorado
Ecological Services Field Office, U.S.
Fish and Wildlife Service, 764 Horizon
Drive, Building B, Grand Junction,
Colorado 81506–3946. Submit new
information, materials, comments, or
questions concerning this species to the
Service at the above address.
FOR FURTHER INFORMATION CONTACT:
Allan Pfister, Western Colorado
Supervisor (see ADDRESSES section), by
telephone at (970) 243–2778, by
facsimile at (970) 245–6933, or by
electronic mail at
fw6_sagegrouse@fws.gov.
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DATES:
SUPPLEMENTARY INFORMATION:
Previous Federal Action
On January 18, 2000, the Director of
the Service designated the Gunnison
sage-grouse as a candidate species under
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the Act, with a listing priority of 5. The
Federal Register notice regarding this
decision was not published until
December 28, 2000 (65 FR 82310,
December 28, 2000). Candidates are
species for which the Service has
determined that the species warrants
listing as a threatened or endangered
species, but listing is precluded by
higher listing priorities for other
species. A listing priority of 5 indicates
that there is a high magnitude of threats,
but they are considered non-imminent.
On January 26, 2000, The American
Lands Alliance, Biodiversity Legal
Foundation, and others petitioned the
Service to list the species (Webb 2000).
On January 10, 2001, some of the same
plaintiffs sued the Service alleging the
Service had not made required petition
findings. In 2003, the U.S. District Court
ruled that the Service’s determination
that the Gunnison sage-grouse was a
candidate constituted a 12-month
finding on the petition (American Lands
Alliance v. Gale A. Norton, C.A. No. 00–
2339, (D.D.C., 2003).
The 2003 Candidate Notice of Review
elevated the species’ listing priority
number to 2 (69 FR 24876), as the
imminence of the perceived threats had
increased. The 2004 Candidate Notice of
Review (70 FR 24870) maintained the
listing priority number as a 2.
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 includes a
provision that the Service would make
a listing determination by March 31,
2006. On March 28, 2006, the plaintiffs
agreed to a one week extension (April 7,
2006) for this determination.
Section 4(b)(1)(A) of the Act requires
us to consider the best scientific and
commercial data available as well as
efforts being made by States or other
entities to protect a species when
making a listing decision. To meet this
standard we collected information on
the Gunnison sage-grouse, its habitats,
threats, and environmental factors
affecting the species from a wide array
of sources. Most of the available
scientific literature on Gunnison sagegrouse is summarized in the Gunnison
Sage-grouse Rangewide Conservation
Plan, a document published in April
2005 under the auspices of the
Gunnison Sage-grouse Rangewide
Steering Committee [GSRSC]. The
GSRSC is comprised of biologists from
state and Federal agencies with
responsibility for managing the
Gunnison sage-grouse or its habitat. The
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scientific literature on Gunnison sagegrouse and its sagebrush habitats is
limited. Where information on
Gunnison sage-grouse life history was
lacking, we used, as appropriate
information on greater sage-grouse to
analyze habitat usage, threats, and
environmental factors affecting the
Gunnison sage-grouse. In addition we
received a substantial amount of
unpublished information from other
Federal agencies, States, counties,
environmental organizations, and
individuals. We also solicited
information on all Federal, State, or
local conservation efforts currently in
operation or planned for the Gunnison
sage-grouse or its habitats.
In April 2005, Colorado Division of
Wildlife (CDOW) applied to the Service
for a Gunnison sage-grouse
Enhancement of Survival Permit
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). Public comments
and other internal comments from the
Service and CDOW were incorporated
into revisions of the CCAA and
Environmental Assessment; the
documents are scheduled to be finalized
shortly. 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. These participants provide
certain Gunnison sage-grouse 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 activities identified in the
Certificate of Inclusion. Although we
strongly encourage continued
conservation of the Gunnison sage-
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grouse, we did not rely upon this CCAA
to support our listing determination.
Species Information
In this determination, we use
information specific to the Gunnison
sage-grouse where available. However,
where such information is lacking we
use information on life history, habitat
requirements, and effects of threats on
greater sage-grouse. Except where
referenced, the following life history
information is taken from the Schroeder
et al. (1999) literature review on sagegrouse (Centrocercus spp.).
The sage-grouse is the largest grouse
in North America and was first
described by Lewis and Clark in 1805
(Schroeder et al. 1999). Sage-grouse 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).
For many years sage-grouse were
considered a single species. Young et al.
(2000) identified Gunnison sage-grouse
(Centrocercus minimus) as a distinct
species based on morphological (Hupp
and Braun 1991; Young et al. 2000),
genetic (Kahn et al. 1999; OylerMcCance et al. 1999), and behavioral
(Barber 1991; Young 1994; Young et al.
2000) differences and geographical
isolation. Based on these differences,
the American Ornithologist’s Union
(2000) accepted the Gunnison sagegrouse as a distinct species. The current
ranges of the two species are not
overlapping (Schroeder et al. 2004). We
have considered the Gunnison sagegrouse as a distinct species consistent
with the petition under review here. We
acknowledge that there are questions
regarding the validity of this taxon,
however it is not the purpose of this
action to elucidate taxonomic questions.
The purpose of this action is to
determine the status of the taxon within
the context of the ESA.
Gunnison sage-grouse and greater
sage-grouse have similar life histories
and habitat requirements (Young 1994).
Nesting success for Gunnison sagegrouse is highest in areas where forbs
and grass covers are found below a
sagebrush canopy cover of 15 to 30
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percent (Young et al. 2000). These
numbers are comparable to those
reported for the greater sage-grouse
(Connelly et al. 2000a). Connelly et al.
(2000a) also state that nest success for
greater sage-grouse is greatest where
grass cover is present. Therefore, factors
identified in the greater sage-grouse
literature that affect nesting habitat
quality can affect Gunnison sage-grouse
nesting habitat in a similar manner if
those factors occur within the range of
the Gunnison sage-grouse.
Characteristics of sage-grouse winter
habitats are also similar through the
range of both species (Connelly et al.
2000a). 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;
Young et al. 2000). However, they may
also use areas with more deciduous
shrubs during the winter (Young et al.
2000).
Dietary requirements of the two
species also are similar, being composed
of nearly 100 percent sagebrush in the
winter (Schroeder et al. 1999; Young et
al. 2000). Forbs and insects are
important during the summer and early
fall. Gunnison and greater sage-grouse
do not possess muscular gizzards and,
therefore, lack the ability to grind and
digest seeds (Rasmussen and Griner
1938; Leach and Hensley 1954).
Gunnison sage-grouse chick dietary
requirements of insects and forbs also
are expected to be similar to greater
sage-grouse and other grouse species
(Tony Apa, CDOW, pers. comm. 2005).
In the spring, sage-grouse gather on
traditional breeding areas referred to as
leks (Patterson 1952). Lek displaying
occurs from mid-March through late
May, depending on elevation (Rogers
1964). For Gunnison sage-grouse, 87
percent of all nests were located less
than 6 kilometers (km) (4 miles (mi))
from the lek of capture (Apa 2004).
Mean clutch size for Gunnison sagegrouse is 6.8 ± 0.7 eggs (Young 1994).
Most eggs hatch in June, with a peak
between June 10 and June 20. Renesting
rates following the loss of the original
nest appear very low in Gunnison sagegrouse, with one study reporting 4.8
percent (Young 1994).
During the pre-egg laying period,
female sage-grouse select forbs that have
generally higher amounts of calcium
and crude protein than sagebrush has
(Barnett and Crawford 1994). Chicks are
precocial and leave the nest with the
hen shortly after hatching. Females with
chicks move to areas containing
succulent forbs and insects, often in wet
meadow habitat, where cover is
sufficiently tall to conceal broods and
provide shade. The availability of food
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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; Klebenow and Gray 1968;
Peterson 1970; Johnson and Boyce 1990;
Johnson and Boyce 1991; Drut et al.
1994b; Pyle and Crawford 1996; Fischer
et al. 1996b). Diets of 4- to 8-week-old
greater sage-grouse chicks were found to
have more plant material (Peterson
1970). 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; Connelly and Markham 1983;
Connelly et al. 1988; Fischer et al.
1996b).
During late summer and early fall,
intermixing of broods and flocks of
adult birds is common and the birds
move from riparian areas to sagebrushdominated landscapes that continue to
provide green forbs. From late autumn
through early spring the diet of greater
and Gunnison sage-grouse is almost
exclusively sagebrush (Rasmussen and
Griner 1938; Batterson and Morse 1948;
Patterson 1952; Leach and Hensley
1954; Barber 1968; Wallestad et al.
1975; Young et al. 2000). Many species
of sagebrush can be consumed
(Remington and Braun 1985; Welch et
al. 1988, 1991; Myers 1992). Flock size
in winter is variable (15 to 100+), and
flocks frequently consist of a single sex
(Beck 1977; Hupp 1987). During
particularly severe winters, sage-grouse
are dependent on tall sagebrush, which
is exposed even above deep snow,
providing a consistently available food
source. In response to severe winters,
Gunnison sage-grouse have been
documented to move as far as 27 km (17
mi) (Root 2002). 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. Movements in fall and
early winter (September–December)
exceed 3 km (2 mi).
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).
Higher survival rate of female sagegrouse may be due to sexual
dimorphism (Schroeder et al. 1999).
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). Other factors
affecting survival rates include year and
age (Zablan 1993).
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Habitat
Sage-grouse are sagebrush obligates
(Patterson 1952; Connelly et al. 2000a).
They depend on a variety of shrubsteppe habitats throughout their life
cycle and are considered obligate users
of several species of sagebrush
(Patterson 1952; Braun et al. 1976;
Schroeder et al. 1999; Connelly et al.
2000a; Connelly et al. 2004). Sagebrush
serves as a primary food for adults yearround (Wallestad et al. 1975) and also
provides cover for nests (Connelly et al.
2000a). Sage-grouse move between
seasonal ranges based on suitable
habitat availability. Connelly et al.
(2000a) 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.
Breeding habitat includes leks and
pre-laying, nesting, and early broodrearing areas. Male Gunnison sagegrouse attend leks from mid-March to
mid-May. Leks are typically in the same
location from year to year; some
Gunnison sage-grouse leks have been
used since the 1950s (Rogers 1964). Leks
are usually flat to gently sloping areas
of less than 15 percent grade in broad
valleys or on ridges (Hanna 1936;
Patterson 1952; Giezentanner and Clark
1974; Wallestad 1975; Autenrieth 1981;
Klott and Lindzey 1989). Leks have
good visibility and low vegetation
structure (Tate et al. 1979; Connelly et
al. 1981; Gates 1985), and acoustical
qualities that allow sounds of breeding
displays to carry (Patterson 1952; Wiley
1973, 1974; Bergerud 1988; Phillips
1990). Leks are often surrounded by
denser shrub-steppe cover, which is
used for escape, thermal, and feeding
cover. Leks can be formed
opportunistically at any appropriate site
within or adjacent to nesting habitat
(Connelly et al. 2000a) and, therefore,
lek habitat availability is not considered
to be a limiting factor for sage-grouse
(Schroeder 1997). A relatively small
number of dominant males accounts for
the majority of breeding on each lek
(Schroeder et al. 1999).
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;
Connelly et al. 2000a).
Nesting occurs from mid-April to
June. Gunnison sage-grouse typically
select nest sites under sagebrush cover
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with some forb and grass cover (Young
1994), and successful nests were found
in higher shrub density and greater forb
and grass cover than unsuccessful nests
(Young 1994). The sagebrush 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; Connelly et al. 2000a; Connelly et
al. 2004). Shrub canopy and grass cover
provide concealment for sage-grouse
nests and young, and are critical for
reproductive success (Barnett and
Crawford 1994; Gregg et al. 1994;
DeLong et al. 1995; Connelly et al.
2004). 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).
Young (1994) found that radio-tracked
Gunnison sage-grouse nested an average
of 4.3 km (2.7 mi) from the lek nearest
to their capture site, with almost half
nesting within 3 km (2 mi) of their
capture site. 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).
Female sage-grouse have been
documented to travel more than 20 km
(13 mi) to their nest site after mating
(Connelly et al. 2000a). Female
Gunnison and greater sage-grouse
exhibit fidelity to nesting locations
(Connelly et al. 1988; Young 1994; Lyon
2000, Connelly et al. 2004, Holloran and
Anderson 2005). 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; Connelly et al. 2004).
However, there is no statistical
indication that movement to new
nesting areas results in increased
nesting success (Connelly et al. 2004).
Early brood-rearing habitat is found
close to nest sites (Connelly et al.
2000a), although individual females
with broods may move large distances
(Connelly 1982; as cited in Connelly et
al. 2000a). Young (1994) 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 hay
meadows, but were often flushed from
interfaces of wet meadows and habitats
providing more cover, such as sagebrush
or willow-alder (Salix-Alnus). Forbs and
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insects are essential nutritional
components for sage-grouse chicks
(Klebenow and Gray 1968; Johnson and
Boyce 1991; Connelly et al. 2004).
Therefore, early brood-rearing habitat
must provide adequate cover adjacent to
areas rich in forbs and insects to assure
chick survival during this period
(Connelly et al. 2004).
As fall approaches sage-grouse move
from riparian to upland areas and start
to shift to a winter diet (GSRSC 2005).
By late summer and into the early fall,
individuals become more social, and
flocks are more concentrated (Patterson
1952). This is the period when
Gunnison sage-grouse can be observed
in atypical habitat such as agricultural
fields (Commons 1997). However, radiotracking studies in the Gunnison Basin
have found that broods typically do not
use hay meadows further away than 50
meters (m) (165 feet [ft]) of the edge of
sagebrush stands (Gunnison Basin
Conservation Plan 1997).
Movements to winter ranges are slow
and meandering. Sagebrush stand
selection in winter is influenced by
snow depth (Patterson 1952; Connelly
1982 as cited in Connelly et al. 2000a)
and in some areas, topography (Beck
1977; Crawford et al. 2004). 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)
associated with drainages, ridges, or
southwest aspects with slopes less than
15 percent (Wallestad 1975; Beck 1977).
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 roosts’’ (Back et al. 1987).
Hupp and Braun (1989) 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. In
these conditions, the tall and vigorous
sagebrush typical in drainages was an
especially important food source.
Historical Distribution
Based on historical records, museum
specimens, and potential sage-grouse
habitat, Schroeder et al. (2004)
concluded that Gunnison sage-grouse
historically occurred in southwestern
Colorado, northwestern New Mexico,
northeastern Arizona, and southeastern
Utah. Accounts of Gunnison sage-grouse
in Kansas and Oklahoma, as suggested
by Young et al. (2000), are not
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supported with museum specimens, and
Schroeder et al. (2004) found
inconsistencies with the historical
records and the sagebrush habitat
currently available in those areas.
Applegate (2001) 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). The GSRSC
(2005) modified the historic range from
Schroeder et al. (2004), based on more
complete knowledge of historic and
current habitat and the distribution of
the species (GSRSC 2005). Based on this
information, the maximum Gunnison
sage-grouse historical (presettlement)
range is estimated to have been 55,350
square kilometers (sq km) (21,370
square miles [sq mi]) (GSRSC 2005). 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 occupied, or what the total
population was.
Rogers (1964) qualitatively discussed
a decrease in sagebrush range due to
overgrazing from the 1870’s until about
1934. Additional 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 (Rogers
1964). Rogers (1964) discussed
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sagebrush eradication (by spraying and
burning) in the 1950s, and used two
examples (Uncompaghre Plateau,
Flattop Mountain in Gunnison County,
CO) within the current range to
illustrate the large acreages (3–5,000
acres) treated, but stated that long-term
effects were yet to be determined.
Rogers (1964) demonstrated a much
broader distribution of sagebrush in
Colorado than what currently exists.
Rogers (1964) also presents maps that
show decreases in distribution from
previous literature.
Much of what was once sagebrush
was already lost prior to 1958. Through
the use of low-level aerial photography,
Oyler-McCance et al. (2001)
documented a loss of only or 155,673 ha
(20 percent) of sagebrush habitat from
1958 to 1993 within Gunnison sagegrouse range. Thirty-seven percent of
the plots sampled underwent
substantial fragmentation of sagebrush
vegetation during that same time period.
Oyler-McCance et al. (2001) stated that
sage-grouse habitat in southwestern
Colorado (the range of Gunnison sagegrouse) has been more severely
impacted than sagebrush habitat
elsewhere in Colorado. However, the
Gunnison Basin was not as significantly
affected as other areas.
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
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of sagebrush habitat. These projects
provide water storage and, to a certain
extent, facilitate agricultural activities
throughout the range of Gunnison sagegrouse.
Riebsame et al (1996) discussed a
greater rural growth rate in Colorado
from the 1970s through the 1990s,
compared to the rest of the U.S., which
has resulted in land use conversion.
They noted a pattern of private ranches
shifting to residential communities
within Gunnison sage-grouse habitat.
The Gunnison Basin Working Group
Research Sub-committee (February,
2006) cited two regions within the Basin
to be of the highest priority for
conservation easements due to
development pressures.
In summary, a substantial amount of
sagebrush habitat within the range of
the Gunnison sage-grouse had been lost
prior to 1960. In the years since, habitat
loss and fragmentation has slowed,
although development pressures have
been on the rise. Conservation efforts
are being developed to help address
development-related issues.
Current Distribution and Population
Estimates
Gunnison sage-grouse currently occur
in seven widely scattered and isolated
populations in Colorado and Utah,
occupying 4,720 sq km (1,820 sq mi)
(GSRSC 2005). 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 seven
populations is presented in Table 1.
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TABLE 1.—POPULATION SIZE, EXTENT OF OCCUPIED HABITAT, LAND OWNERSHIP, AND URBAN DEVELOPMENT PRESSURES
Population size
range
1995–2005*
2005 population
estimate
Currently
occupied area
Gunnison Basin
Population.
2,203–4,763 .....
4,763 ................
240,000 hectares (ha)
593,000 (ac).
51 percent BLM, 14 percent Gunnison County currently has a
USFS, 2 percent NPS, 1 perlow population density of 5
cent CDOW, 1 percent Colopeople/sq mi in 2000 (GSRSC
rado State Land Board, 31
2005), with projected growth
percent private (GSRSC 2005).
rates ranging from .1 to 1.6
percent per year. These rates
result in a population increase
of about 5700 people by 2030
(41 percent or 7 people/sq mi)
(CDLA 2004). A 30 percent
housing increase is projected
from 2000–2020 (GSRSC
2005).
San Miguel Basin
Population.
206–446 ...........
334 ...................
40,500 ha
(100,500 ac).
Dry Creek—57 percent BLM, 12
percent, CDOW, 1 percent,
Colorado State Land Board,
30 percent private.
Hamilton Mesa—85 percent private, 11 percent Colorado
State Land Board, 4 percent
BLM.
Miramonte—76 percent private,
15 percent CDOW, 7 percent
USFS, 2 percent BLM.
Gurley Reservoir—91 percent
private, USFS 4 percent, BLM
3 percent, the Colorado State
Land Board 2 percent.
Beaver Mesa—99.5 percent private, 0.5 percent BLM.
Iron Springs—89 percent private, 6 percent USFS, 5 percent Colorado State Land
Board (GSRSC 2005).
The population in San Miguel
County is expected to double
to 18 people/sq mi between
2000 and 2030 (CDLA 2004),
accompanied by a 62 percent
increase in housing units by
2020 (GSRSC 2005).
Monticello-Dove
Creek Population.
162–510 (Combined).
196 (162 Monticello and 34
Dove Creek).
40,000 ha
(98,920 ac)
(Combined).
Monticello—95 percent private, 4
percent BLM, 1 percent State
of Utah land.
The Monticello, UT group has
approximately 2 people/sq mi
(GSRSC 2005) with a projected increase of roughly
18% to 2600 people (2.4 people/sq mi) by 2030 (Utah Governor’s Office of Planning and
Budget 2005).
123–280 (Monticello).
..........................
Dove Creek—87 percent privately owned, 13 percent BLM
(GSRSC 2005).
10–358 (Dove
Creek).
..........................
Monticello—
28,500 ha
(71,000 ac).
Dove Creek—
11,500 ha
(28,000 ac).
79–206 .............
167 ...................
16,000 ha
(39,000 ac).
70 percent private, 28 percent
BLM,
2
percent
USFS
(GSRSC 2005).
Name of
population
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˜
Pinon Mesa Population.
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Development pressure
Population density of 55 people/
sq mi in 2000 (GSRSC 2005)
with a projected increase to
105 people/sq mi by 2030
(CDLA 2004).
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TABLE 1.—POPULATION SIZE, EXTENT OF OCCUPIED HABITAT, LAND OWNERSHIP, AND URBAN DEVELOPMENT
PRESSURES—Continued
Population size
range
1995–2005*
2005 population
estimate
Crawford Population.
118–314 ...........
191 ...................
Cerro SummitCimarron-Sims
Mesa Population.
Poncha Pass
Population.
25–83 ...............
5–44 .................
Name of
population
Currently
occupied area
Land ownership
Development pressure
14,000 ha
(35,000 ac).
63 percent BLM, 13 percent
NPS, 24 percent private
(GSRSC 2005).
Estimate of 24 people/sq mi living in and near this population
in 2000 (GSRSC 2005).
Montrose County contains the
southeastern 75 percent of the
current range of the Crawford
population. The county was
identified as one of the fastest
growing counties in the country, with human population expected to double from 2000–
2030 (CDLA 2004) and housing expected to increase by
68 percent by 2020. The
northwestern 25 percent of the
current range is in Delta
County, which is projected to
increase in population by 79
percent by 2030 (CDLA 2004)
with an increase in housing of
58 percent by 2020 (GSRSC
2005).
25 .....................
15,000 ha
(37,000 ac).
43 percent private, 51 percent
BLM, 6 percent CDOW
(GSRSC 2005).
Population threats not evaluated.
44 .....................
8,300 ha
(20,400 ac).
48 percent BLM, 26 percent
USFS, 24 percent in private
holdings, 2 percent Colorado
State Land Board (GSRSC
2005).
Population threats not evaluated.
rwilkins on PROD1PC63 with RULES_2
* The numbers presented are the lowest and highest population estimates during the 11-year period. The lows and highs did not all fall in the
same years for each population.
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). Big
sagebrush (Artemesia tridentata)
dominates the upland vegetation and
has a highly variable growth form
depending on local site conditions. Up
to 84 leks have been surveyed annually
for breeding activity in the Gunnison
Basin (CDOW, unpubl. lit. 2005a).
Approximately 37 percent of these leks
occur on private land and 63 percent on
public land, primarily BLM (GSRSC
2005). In 2005, 44 of these leks were
active, 38 inactive, and 2 are of
unknown status. Rogers (1964) stated
that Gunnison County had one of the
largest sage-grouse populations in
Colorado.
San Miguel Basin Population—The
San Miguel Basin population is in
Montrose and San Miguel Counties in
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Colorado, and is composed of six groups
using different areas—Dry Creek Basin,
Hamilton Mesa, Miramonte Reservoir,
Gurley Reservoir, Beaver Mesa, and Iron
Springs. Some of these six areas are
used year-round by sage-grouse, and
others are used seasonally. Recent
radiotelemetry studies have suggested
that sage-grouse in the San Miguel Basin
move widely and between these areas
(Apa 2004; Stiver, unpubl. lit. 2005).
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).
Gunnison sage-grouse use the Hamilton
Mesa area in the summer, but use
during other seasons is unknown.
Miramonte Reservoir occupied sagegrouse habitat is approximately 4,700 ha
(11,600 ac) (GSRSC 2005). Sagebrush
stands are generally contiguous with a
mixed grass and forb understory.
Occupied habitat at the Gurley
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Reservoir area is heavily fragmented 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 now are restricted
primarily to the seasonal irrigation 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). Sagebrush stands in the Iron
Springs and Beaver Mesa areas are
contiguous with a mixed grass
understory. The Beaver Mesa area has
numerous scattered patches of oakbrush
(Quercus gambelii).
The 2005 population estimate for the
entire San Miguel Basin was 334
(CDOW, unpubl. lit. 2005b) on 9 leks.
Rogers (1964) reported that all big
sagebrush-dominated habitats in San
Miguel and Montrose Counties were
historically used by sage-grouse. The
historic distribution was highly
fragmented by forests, rocky canyons
and dry basins void of sagebrush
habitats.
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Monticello-Dove Creek Population—
This population has two disjunct groups
of Gunnison sage-grouse. Currently, the
largest group is near the town of
Monticello, Utah. Gunnison sage-grouse
in this group 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) estimates that Gunnison sagegrouse currently occupy about 24,000 ha
(60,000 ac) in the Monticello group. The
2005 population estimate for Monticello
was 162 individuals with 2 active and
2 inactive leks (G. Wallace, UDWR pers.
comm. 2005). Leks in the Monticello
area were first identified and counted in
1968.
The Dove Creek group 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 7 males in 2005
(CDOW, unpubl. lit. 2005c). All leks are
located in agricultural fields on private
lands. 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; Apa 2004).
Rogers (1964) reported that all
sagebrush-dominated habitats in
Dolores and Montezuma Counties
within Gunnison sage-grouse range in
Colorado were historically used by sagegrouse.
˜
˜
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. Eight leks are known (CDOW,
unpubl. lit. 2004). However, one is
inactive and another was not active in
2005 (CDOW unpubl. lit. 2005d). 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 makes locating
additional leks difficult. Gunnison sagegrouse 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). Their current distribution
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has been substantially reduced from
historic levels (GSRSC 2005).
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 (A. t.
tridentata) and black sagebrush (A.
nova) dominate the mid-elevation
uplands (GSRSC 2005). The 2005
population estimate for Crawford is 191
(CDOW, unpubl. lit. 2005e). Currently
there are four active leks 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).
Cerro Summit-Cimarron-Sims Mesa
Population—This population is in
Montrose County, Colorado. The Cerro
Summit-Cimarron group is centered
about 24 km (15 mi) east of Montrose.
The habitat consists of patches of
sagebrush habitat fragmented by
oakbrush and irrigated pastures. Three
leks are known in the Cerro SummitCimarron group, but only one was
verified to be active in 2005. Rogers
(1964) 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 is inactive.
Rogers (1964) counted eight males in a
lek count at Sims Mesa in 1960. It is not
known if sage-grouse move between the
Cerro-Summit-Cimarron and Sims Mesa
groups.
Poncha Pass Population—The Poncha
Pass sage-grouse population is located
in Saguache County, approximately 16
km (10 mi) northwest of Villa Grove,
Colorado. This population was
established through the introduction of
30 birds from the Gunnison Basin in
1971 and 1972 during efforts to
reintroduce the species to the San Luis
Valley (GSRSC 2005). The known
population distribution is in 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 extensive and
continuous with little fragmentation;
sagebrush habitat quality throughout the
area is adequate (Nehring and Apa
2000). San Luis Creek runs through the
area, providing a year-round water
source and lush, wet meadow riparian
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19961
habitat for brood-rearing. The 2005
Poncha Pass sage-grouse population
estimate is 44 (CDOW, unpubl. lit.
2005f). 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 transplanted 24 additional
birds from the Gunnison Basin (Nehring
and Apa 2000). In 2001 and 2002, 20
and 7 birds respectively also were
moved to the Poncha Pass by CDOW
(GSRSC 2005). Transplanted females
have bred successfully (Apa, CDOW,
pers. comm. 2004) and display activity
resumed on the historic lek in spring
2001.
Population Trends
Trends in abundance were analyzed
for individual populations and the
species rangewide using male lek count
data from CDOW and UDWR (Garton
2005). Due to inconsistencies in data
collection over time, trend analyses
were conducted for two time periods—
the entire number of years lek data have
been collected (1957–2005), and from
1995–2005 when sampling
methodologies have been more
consistent. Raw data collected for 2005
show a large increase in the numbers of
males attending leks. Because of this,
the analyses were conducted both with
and without 2005 data; estimates did
not change significantly when the 2005
lek counts were omitted in this analysis.
Statistical analyses of the Cerro SummitCimarron-Sims Mesa and Dove Creek
populations could not be completed due
to low lek counts and inconsistencies in
sampling over time. Similarly, the small
Poncha Pass population was not
analyzed because it has been surveyed
for only 6 years and in that time the
population was augmented with birds
from Gunnison Basin.
The long-term analysis (1957–2005)
found that the rangewide population of
Gunnison sage-grouse was neither
increasing nor decreasing during that
time period. Annual rates of change
were highly variable, most likely as a
result of sampling error rather than
actual changes in population sizes. The
shorter analysis period (1995–2005)
yielded the same results, although the
variability was reduced, likely due to
more consistent data collection
methods. Individual populations
reflected the trends in the rangewide
analysis, in that some populations were
slightly increasing and some were
slightly decreasing (Table 2). As with
similar analyses conducted for the
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habitat loss over time was not accounted
for, that population declines would go
unnoticed, and that population trends
would appear far too optimistic.
An identical population trend
analysis was peer reviewed by the
TABLE 2.—SUMMARY OF POPULATION Ecological Society of America in the
TRENDS FOR THE GUNNISON SAGE- ‘‘Conservation Assessment of Greater
Sage-grouse and Sagebrush Habitats’’
GROUSE 1
(Connelly et al. 2004). Additional
clarifying information regarding model
Finite
Population
rate of assumptions, the primary concern of the
change peer reviewers, was provided by Garton
after the peer review was complete.
Rangewide ........................................
1.049
Based on this late submission, and after
Gunnison Basin ................................
1.05
careful review of the analysis, we
˜
Pinon Mesa .......................................
1.09
believe that Garton (2005) constitutes
San Miguel Basin ..............................
0.9
Crawford ...........................................
0.999 the best currently available information.
greater sage-grouse (Connelly et al.
2004), density-dependent models
appeared to more accurately describe
observed population trends (Garton
2005).
Monticello ..........................................
0.99
1 Values
rwilkins on PROD1PC63 with RULES_2
are the finite rate of change in the
population, where 1 is no change, numbers
less than 1 indicate a decline, and numbers
greater than 1 indicate an increase. The analysis is for 1995–2005 (data from Garton
2005).
Because we relied on the population
trend analyses conducted by Garton
(2005), we asked six peer reviewers to
evaluate the report. We received
comments from five of the reviewers,
three generally favorable towards the
report and its conclusions and two
expressing concerns regarding
limitations in the data sets,
assumptions, and/or analyses. For
example, one would have to assume that
habitat availability over time would
remain stable in order to conclude that
Gunnison sage-grouse numbers are
unlikely to experience a substantial
decline in the future. Also, while the
conclusions showed that the number of
males per lek remained relatively stable
over time, the proportion of leks on
which males were counted appeared to
have declined, which could be
indicative of an overall population
decline. In discussing the historic
distribution of Gunnison sage-grouse,
we concluded that much of the habitat
loss, and by inference population
decline, occurred prior to 1958.
It was also suggested that more
appropriate statistical tests would need
to be applied to come to any conclusion
about potential population trends and
that emphasis should be on an
independent analysis of each
geographically isolated population
because each population exhibits
independent population dynamics.
Population trend analyses were
conducted on a population basis (as
well as rangewide). However, to further
subdivide the data analyzed into smaller
units (i.e. subpopulations) would have
compromised the statistical integrity of
the analysis due to small sample sizes.
There was concern expressed that
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Summary of Factors Affecting the
Species
Section 4 of the Act (16 U.S.C. 1533)
and regulations (50 CFR part 424)
promulgated to implement the listing
provisions of the Act set forth the
procedures for adding species to the
Federal lists. A species may be
determined to be an endangered or
threatened species due to one or more
of the five factors described in section
4(a)(1). As part of our analysis, we
chose, out of an abundance of caution,
not to rely on the Cerro SummitCimarron-Sims Mesa and Poncha Pass
populations and the Dove Creek group
of the Monticello-Dove Creek
population for the longterm
conservation of the species because of
their small, isolated status. We also
determined that these populations do
not comprise a significant portion of the
Gunnison sage-grouse range. Therefore,
these populations/group were not
evaluated further for future threats.
Although we are not relying on these
populations/group for the longterm
conservation of the species, we
nonetheless believe that conservation of
these populations is worthwhile, and
we will continue to support and
encourage those efforts. However, we
analyze the threats applicable to the
remaining populations/group to
determine whether the species as a
whole meets the definition of threatened
or endangered.
The Service considers the foreseeable
future in Gunnison sage-grouse to be
between 30 and 100 years based on 10
Gunnison sage-grouse generations to 2
sagebrush habitat regeneration cycles.
This is consistent with our 12-month
finding for the greater sage-grouse (70
FR 2244). Because the Gunnison sagegrouse has the same generation time and
occupies habitat similar to the greater
sage-grouse, we consider it prudent to
use the same definition for the
foreseeable future.
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A. The Present or Threatened
Destruction, Modification, or
Curtailment of Its Habitat or Range
Data indicate that the Gunnison sagegrouse was found in central and
southwest Colorado, southeast Utah,
northwestern New Mexico, and
northeastern Arizona prior to European
settlement (GSRSC 2005, modified from
Schroeder et al. 2004). Gunnison sagegrouse currently occupy 4,719 sq km
(1,822 sq mi) in southwestern Colorado
and southeastern Utah (GSRSC 2005,
modified from Schroeder et al. 2004).
The following describes the issues
affecting Gunnison sage-grouse within
their current range.
Current Threats Due to Habitat
Fragmentation: Habitat fragmentation is
the separation or splitting apart of
previously contiguous, functional
habitat. Fragmentation of sagebrush
habitats has been cited as a primary
cause of the decline of sage-grouse
populations (Patterson 1952; Connelly
and Braun 1997; Braun 1998; Johnson
and Braun 1999; Connelly et al. 2000a;
Miller and Eddleman 2000; Schroeder
and Baydack 2001; Aldridge and
Brigham 2003; Connelly et al. 2004;
Schroeder et al. 2004). While sagegrouse are dependent on interconnected
expanses of sagebrush (Patterson 1952;
Connelly et al. 2004), data are not
available regarding optimum or even
minimum sagebrush patch sizes
necessary to support sage-grouse
populations. In addition, there is a lack
of data to assess how fragmentation
influences specific sage-grouse lifehistory parameters such as productivity,
density, and home range.
Oyler-McCance et al. (2001)
documented loss and fragmentation of
sagebrush vegetation in southwestern
Colorado. In a genetic study of
Gunnison sage-grouse populations,
Oyler-McCance et al. (2005) concluded
that gene flow among populations of
Gunnison sage-grouse is limited.
Notwithstanding the lack of
specificity on effects of fragmentation, it
is clear that as a whole, fragmentation
can have an adverse effect on sagegrouse populations. The following
sections examine activities that can
contribute to habitat fragmentation to
determine whether they threaten
Gunnison sage-grouse habitat.
Conversion to Agriculture and Water
Development
In the mid-1800s, western rangelands
were converted to agricultural lands on
a large scale beginning with the series
of Homestead Acts in the 1800s (Braun
1998; Hays et al. 1998), especially
where suitable deep soil terrain and
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water were available (Rogers 1964).
Influences resulting from agricultural
activities adjoining sagebrush habitats
extend into those habitats, and include
increased predation and reduced nest
success due to predators associated with
agriculture (Connelly et al. 2004).
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 sage-grouse (C. Braun, CDOW,
pers. comm. 1998). However, crop
monocultures do not provide adequate
year-round food or cover (GSRSC 2005).
Gunnison sage-grouse will use hay
pastures for foraging within about 50 m
(165 ft) of the edge of the field but do
not forage further into the pasture due
to lack of suitable habitat (Gunnison
Basin Conservation Plan 1997).
In the Gunnison Basin approximately
17,328 ha (42,800 ac) or 8 percent of the
current range was converted to
agricultural activities in the past and for
the most part is no longer occupied
(GSRSC 2005). Approximately 5,700 ha
(14,000 ac) or 7 percent of the current
range in the San Miguel Basin has been
converted to agriculture and for the
most part is unoccupied (GSRSC 2005).
The arrangement of these converted
lands has contributed to habitat
fragmentation in these areas, although it
is not negatively influencing sage-grouse
numbers in this population (Garton
2005).
Approximately 30 percent of the
40,048 ha (98,920 ac) of the current
range in the Monticello-Dove Creek
population has been converted to
agriculture and for the most part is no
longer occupied (GSRSC 2005). In the
Monticello group, 43 percent has been
converted to pasture (GSRSC 2005). San
Juan County, Utah, where the
Monticello group resides, also has
approximately 15,000 ha (37,000 ac)
enrolled in Conservation Reserve
Program (CRP), of which about half is
within current sage-grouse range (San
Juan County Gunnison Sage-grouse
Work Group [GSWG], unpubl. lit. 2005;
GSRSC 2005). Under CRP, cropland is
planted to pastureland and, except in
emergency situations, not hayed or
grazed. The CRP fields are used heavily
by grouse as brood-rearing areas but
vary greatly in plant diversity and forb
abundance, and generally lack any
shrub cover (GSRSC 2005). Sagebrush
patches have progressively become
smaller and more fragmented limiting
the amount of available winter habitat
for the Monticello group (GSRSC 2005).
Significant use of CRP as nesting or
winter habitat will require
establishment of sagebrush stands in
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these fields. The CRP has protected this
area from more intensive agricultural
use and development, and
approximately 16,000 ha (40,000 ac) of
CRP are up for renewal under the Farm
Bill in the next 2–3 years.
Conversion to agriculture is limited in
˜
the Pinon Mesa area, with only 5
percent (500 ha (1,214 ac)) of the current
range planted to grass/forb rangeland
and for the most part no longer
occupied (GSRSC 2005). Sagebrush
occurs in some areas that may be
converted to grassland for livestock
(BLM, unpubl. lit. 2005a), but the
continued conversion is considered to
be a minor impact in the foreseeable
future. Habitat conversion in the
Crawford area due to agricultural
activities has been limited (GSRSC
2005).
Although past conversion to
agriculture has resulted in the loss of
sagebrush habitat, we have no evidence
to conclude that ongoing or anticipated
agricultural conversion of sagebrush
habitats is likely to threaten or endanger
the Gunnison sage-grouse. Existing
agricultural activities may fragment the
species current range, but we have no
data to determine that this is actually
occurring, or is likely to occur.
Past development of irrigation
projects has also resulted in loss of sagegrouse habitat (Braun 1998). Reservoir
development in the Gunnison Basin
flooded 3,700 ha (9,200 ac or 1.5
percent) of likely sage-grouse habitat (S.
McCall, Bureau of Reclamation, pers.
comm. 2005), and three other reservoirs
inundated approximately 2 percent of
habitat in the San Miguel Basin
population area (J. Garner, CDOW, pers.
comm. 2005). We are unaware of any
plans for additional reservoir
construction in the foreseeable future
and do not consider water development
a threat to the species.
Roads
Impacts from roads may include
direct habitat loss, direct mortality,
creation of barriers to migration to
seasonal habitats (Forman and
Alexander 1998), facilitation of
mammalian (Forman and Alexander
1998; Forman 2000) and corvid
predation (Connelly et al. 2000b;
Aldridge and Brigham 2003; Connelly et
al. 2004) and expansion into previously
unused areas, spread of invasive weeds
(Forman and Alexander 1998; Forman
2000; Gelbard and Belnap 2003; Knick
et al. 2003; Connelly et al. 2004), noise
in the vicinity of leks (Braun 1986;
Forman and Alexander 1998; Holloran
2005), and increased recreational use
and associated human disturbances
(Forman and Alexander 1998; Massey
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2001; Wyoming Game and Fish
Department 2003). Specific effects of
these factors on sage-grouse are
discussed below.
Lyon (2000) suggested that roads may
be the primary impact of oil and gas
development to greater sage-grouse, due
to their persistence and continued use
even after drilling and production have
ceased. Braun et al. (2002) suggested
that daily vehicular traffic along road
networks for oil wells can impact
Gunnison and greater sage-grouse
breeding activities based on a
documented decrease in males at leks.
Modeling done in Connelly et al. (2004)
found that the number of active leks, lek
persistence and lek activity increased
with increasing distance from an
interstate highway. Other than this
single predictive model output, we have
no quantitative information on the
current impact of roads to Gunnison
sage-grouse. It is unclear what specific
factor relative to roads sage-grouse are
responding to, and Connelly et al.
(2004) caution that they have not
included other potential sources of
disturbance (e.g., powerlines) in their
analyses.
Roads may have additional indirect
effects that result from birds’ behavioral
avoidance of road areas because of
noise, visual disturbance, pollutants,
and predators moving along them. The
absence of screening vegetation in arid
and semiarid regions further exacerbates
any problems (Suter 1978). Male sagegrouse depend on acoustical signals to
attract females to leks (Gibson and
Bradbury 1985; Gratson 1993). If noise
interferes with mating displays, and
thereby female attendance, it is possible
that younger males will not be drawn to
the lek and eventually leks will become
inactive (Braun 1986; Holloran 2005).
Dust from roads and exposed roadsides
can damage vegetation through
interference with photosynthetic
activities; the actual amount of potential
damage depends on winds, wind
direction, the type of surrounding
vegetation and topography (Forman and
Alexander 1998). Chemicals used for
road maintenance, particularly in areas
with snowy or icy precipitation, can
affect the composition of roadside
vegetation (Forman and Alexander
1998). While all of these potential
effects are actually occurring or whether
they have actually affected sage-grouse
populations individually or at a species
level.
Gunnison sage-grouse habitat is
currently fragmented by a number of
roads (BLM, unpubl. lit. 2005b,
Colorado Department of Transportation
(CDOT) 2004, Jim Ferguson, BLM, pers.
comm. 2005, San Juan County GSWG,
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unpubl. lit. 2005), and road
development within Gunnison sagegrouse habitats has precluded sagegrouse movement between the resultant
patches (Oyler-McCance et al. 2001).
New roads and increased traffic on
existing roads may cause some impact
to the Dry Creek Basin birds in the San
Miguel Basin, primarily due to ongoing
gas field development and exploration
on both the eastern and western edges
of the current range. Increases in truck
traffic have been noted on 24 km (15 mi)
of roads that cross the center of the
current range in Dry Creek Basin.
However, only two sage-grouse have
been killed on the roads in Dry Creek
Basin since 2003 (CDOW, unpubl. lit.
2006). No paved roads occur in the
˜
current range for the Pinon Mesa
population, but with projected human
population increases of 91 percent by
2030 (Colorado Department of Local
Affairs [CDLA] 2004), we anticipate that
new or existing roads will be paved in
the foreseeable future.
This information suggests new roads
may result in additional habitat loss and
fragmentation. It may also increase
disturbance and chance of direct
mortality. However, based on the data
available to us, we have no data to
support that the effects of existing roads
in general, and the new roads
specifically will impact Gunnison sage
grouse at the species level.
Powerlines
The most detrimental effect that
powerlines have is to provide a
convenient perch for predators. There
are reports that they can also directly
affect sage-grouse by posing a collision
and electrocution hazard (Braun 1998;
Connelly et al. 2000a), and can have
indirect effects by increasing predation
(Connelly et al. 2004), fragmenting
habitat (Braun 1998), and facilitating the
invasion of exotic annual plants (Knick
et al. 2003; Connelly et al. 2004).
However, although death through
collision and electrocution are widely
referenced, only one citation actually
provides data to support the claim with
a report of three adult sage-grouse dying
as a result of colliding with a telegraph
line in Utah (Borell 1939). Both Braun
(1998) and Connelly et al. (2000a) report
that sage-grouse collisions with
powerlines occur, although no specific
instances were presented.
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
(Steenhof et al. 1993; Connelly et al.
2000a; Manville 2002; Vander Haegen et
al. 2002). Power poles increase a
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raptor’s range of vision, allow for greater
speed during attacks on prey, and serve
as territorial markers (Steenhof et al.
1993; Manville 2002). Raptors may
actively seek out power poles where
natural perches are limited. For
example, within 1 year of construction
of a 596-km (373-mi) transmission line
in southern Idaho and Oregon, raptors
and common ravens (Corvus corax)
began nesting on the supporting poles
(Steenhof et al. 1993). Within 10 years
of construction, 133 pairs of raptors and
ravens were nesting along this stretch
(Steenhof et al. 1993). The increased
abundance of raptors and corvids within
the current Gunnison sage-grouse range
could result in increased predation
(Oyler-McCance et al. 2001). Ellis (1985)
reported that golden eagle predation on
greater sage-grouse increased from 26–
73 percent after completion of a
transmission line within 200 m (656 ft)
of an active sage-grouse lek in
northeastern Utah. The lek was
eventually abandoned. Ellis (1985)
concluded that the presence of the
powerline resulted in changes in sagegrouse dispersal patterns and
fragmentation of the habitat. 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 (Braun et al. 2002). The
presence of a powerline may fragment
sage-grouse habitats even if raptors are
not present. Braun (1998) found that use
of otherwise suitable habitat by sagegrouse near powerlines increased as
distance from the powerline increased
for up to 600 m (1,969 ft) and reported
that the presence of powerlines may
limit sage-grouse use within 1 km (0.6
mi) in otherwise suitable habitat.
Linear corridors through sagebrush
habitats can facilitate the spread of
invasive species, such as cheatgrass
(Bromus tectorum) (Connelly et al.
2004). However, we were unable to find
any information regarding the amount of
invasive species incursion as a result of
powerline construction.
On 121,000 ha (300,000 ac) of BLM
land in Gunnison Basin there are 36
rights-of-way for power facilities, power
lines, and transmission lines, which
have resulted in the direct loss of 350
ha (858 ac) of occupied habitat (BLM,
unpubl. lit. 2005c). A transmission line
runs through the Dry Creek Basin group
in the San Miguel Basin population, and
the Beaver Mesa group has two. None of
the transmission lines in the San Miguel
Basin have raptor proofing (BLM,
unpubl. lit. 2005d), nor do most
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distribution lines (Jim Ferguson, BLM,
pers. comm. 2005). One major electric
transmission line runs east-west in the
northern portion of the current range of
the Monticello group (San Juan County
GSWG, unpubl. lit. 2005). Powerlines
do not appear to be present in sufficient
density to pose a significant threat to
˜
Gunnison sage-grouse in the Pinon 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 (J. Ferguson, BLM, pers. comm.
2005). The projected human population
growth rate in and near Gunnison sagegrouse populations is low (see
discussion under urban development).
Therefore we expect a low rate of
increase in powerlines with a
concomitant small increase in predation
from raptors and corvids. We do not
expect these to be substantial threats at
the population level.
Fences
Fences are used to delineate property
boundaries and to manage livestock
(Braun 1998; Connelly et al. 2000a). The
effects of fencing on sage-grouse include
direct mortality through collisions,
creation of predator (raptor) perch sites,
the potential creation of a predator
corridor along fences (particularly if a
road is maintained next to the fence),
and incursion of exotic species along
the fencing corridor (Call and Maser
1985; Braun 1998; Connelly et al. 2000a;
Knick et al. 2003; Connelly et al. 2004).
Sage-grouse frequently fly low and
fast across sagebrush flats and new
fences can create a collision hazard (Call
and Maser 1985). Thirty-six carcasses of
greater sage-grouse were found near
Randolph, Utah, along a 3.2-km (2-mi)
fence within 3 months of its
construction (Call and Maser 1985).
Twenty-one incidents of mortality
through fence collisions near Pinedale,
Wyoming, were reported in 2003 to the
BLM (Connelly et al. 2004). Fence
collisions continue to be identified as a
source of mortality for both Gunnison
and greater sage-grouse (Braun 1998;
Connelly et al. 2000a; Oyler-McCance et
al. 2001; Connelly et al. 2004, San Juan
County GSWG, unpubl. lit. 2005),
although effects on populations are not
understood. Braun (1998) suggested that
collision with fences, especially woven
wire fences, was a potential factor in
sage-grouse decline. Connelly et al.
(2000a) noted that grouse have been
observed hitting or narrowly missing
fences and that grouse remains are
frequently found next to fences. The
impact of collisions on populations of
grouse has not been investigated.
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Fences provide perch sites for avian
predation and, depending on their
design, may also cause habitat loss and
fragmentation. Where there are
maintained trails alongside the fence,
invasive weeds may increase (Connelly
et al. 2000a; Oyler-McCance et al. 2001;
Braun et al. 2002; Gelbard and Belnap
2003; Knick et al 2003; Connelly et al.
2004). Where sage-grouse avoid habitat
adjacent to fences, presumably to
minimize the risk of predation, habitat
fragmentation occurs even if the actual
habitat is not removed (Braun 1998).
There are at least 1,540 km (960 mi)
of fence within BLM lands within the
Gunnison Basin (BLM, unpubl. lit.
2005e) and an unquantified amount on
other land ownerships. While these
fences contribute to habitat
fragmentation in this area 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. Because we do not expect a
major increase in the number of fences
and Gunnison sage-grouse populations
are relatively stable in the affected areas,
we do not believe fencing is a
significant threat to Gunnison sagegrouse at the species level.
Urban Development
It is estimated that 3–5 percent of all
sage-grouse historical habitat in
Colorado has been converted into urban
areas (Braun 1998). Interrelated effects
from urban/suburban development
include construction of associated
infrastructure (roads, powerlines, and
pipelines), which has been discussed, as
well as predation threats from the
introduction of domestic pets and
increases in predators subsidized by
human activities (e.g., landfills). Urban
expansion into rural areas also is
resulting in direct habitat loss and
conversion, as well as alteration of
remaining sage-grouse habitats around
these areas due to the presence of
humans and pets (Braun 1998; Connelly
et al. 2000a). Specific affects of these
factors on sage-grouse are discussed
below.
U.S. Census Bureau projections show
that human population growth varies
widely across the current distribution of
Gunnison sage-grouse (CDLA 2004).
Public ownership in the Crawford area
and Gunnison Basin, and portions of the
San Miguel Basin will limit potential
impacts from development in those
particular areas. However, even these
public lands are intersected by private
lands. ‘‘No development’’ conservation
easements may help alleviate potential
impacts of the expansion effects of
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urban and suburban development
(existing and contemplated conservation
easements in the Gunnison sage-grouse
range are addressed in more detail
under State regulatory protection
considerations in Factor D).
Aldridge (2005) used spatial modeling
to determine various habitat, climatic,
and anthropogenic factors that influence
greater sage-grouse nest and brood
habitat selection and to determine nest
and brood success. He determined that
broods avoided habitats with a high
density of urban development and areas
close to cropland. A single human-use
feature did not appear to affect nest
occurrence but sage-grouse strongly
avoided nesting in areas when roads,
well sites, urban habitats, and cropland
were analyzed in combination. Aldridge
(2005) agreed with Fuhlendorf et al.
(2002) that this may be due to predator
avoidance behavior.
It is possible that residential
development that is not managed to
account for the needs of the Gunnison
sage-grouse could destroy and fragment
habitat for the Gunnison Basin
population. Gunnison County currently
has a low population density of 5
people/sq mi in 2000 (GSRSC 2005),
with projected growth rates ranging
from .1 to 1.6 percent per year. These
rates result in a population increase of
about 5,700 people by 2030 (41% or 7
people/sq mi) (CDLA 2004). A 30
percent housing increase is projected
from 2000–2020 (GSRSC 2005). Growth
from the town of Crested Butte, on the
northern end of the Gunnison Basin
population, is expanding southward.
Population growth estimates are not
available for the portion of Saguache
County that comprises approximately 25
percent of the Gunnison Basin
population’s current range, although
county-wide the projected population
growth from 3 people/sq mi in 2000
(GSRSC 2005) to 2030 is 45 percent
(CDLA 2004). Currently, an estimated
100–500 people live in the Gunnison
Basin portion of Saguache County so the
estimated population in 2030 will be
between 145 and 725 people.
Dry Creek Basin is the only group
within the San Miguel Basin population
with significant Federal and State land
ownership (70 percent). This population
is made up of six disjunct sage-grouse
groups. San Miguel County had 9
people/sq mi in 2000 (GSRSC 2005);
most residents live in the town of
Telluride or several smaller
communities, including Norwood. The
population in San Miguel County is
expected to double to 18 people/sq mi
between 2000 and 2030 (CDLA 2004),
accompanied by a 62 percent increase in
housing units by 2020 (GSRSC 2005).
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Based upon the location of current
subdivided areas, expansion into sagegrouse habitat is certain without some
action by local government (GSRSC
2005). Residential development is likely
to affect the Iron Springs Mesa and
Gurley Reservoir groups (GSRSC 2005).
Subdivision development increased
during 2003 and 2004 and at Gurley
Reservoir, a 260-ha+ (640-ac+) area has
been broken up into 16, 16-ha (40-ac)
tracts for development. Approximately 8
percent of the current range for this
portion of the San Miguel Basin
population will be developed.
Continued development in the area
threatens to cause habitat loss,
fragmentation, and future connection of
the San Miguel Basin population to
other Gunnison sage-grouse
populations. The Miramonte Reservoir
group has a long-term threat of housing
development (GSRSC 2005). However,
the Dry Creek Basin group, which is the
largest and principally in Federal
ownership, has little expected threat
from development (GSRSC 2005).
The Monticello group of the
Monticello-Dove Creek population is in
San Juan County, Utah, which has
approximately 2 people/sq mi (GSRSC
2005) with a projected increase to 3.6
people/sq mi by 2030 (Utah Governor’s
Office of Planning and Budget 2005) and
a 54 percent increase in housing by
2020 (GSRSC 2005). Almost all the
current range in both States is in private
ownership.
˜
The Pinon Mesa population is in
Mesa County, which had a population
density of 55 people/sq mi in 2000
(GSRSC 2005) with a projected increase
to 105 people/sq mi by 2030 (CDLA
2004) and 56 percent in housing units
by 2020 (GSRSC 2005). Approximately
70 percent of the current range is in
private ownership. Expansion of growth
from the nearby city of Grand Junction
poses a threat of permanent habitat loss
and fragmentation. The eastern 33
percent of the current range
(approximately 13,000 ha or 32,000 ac)
is privately-owned and contains 810 ha
(2,000 ac) in tracts, each less than 65 ha
(160 ac), and an additional 1,500 ha
(3,600 ac) in tracts between 65 and 130
ha (160 and 320 ac), all of which can be
further subdivided (GSRSC 2005).
However, 19 percent of the private land
containing all occupied habitat is
currently in conservation easements
with additional lands being negotiated
for conservation easements with the
landowners, thereby limiting the threat
of development (See Factor D for further
discussion of easements).
There were an estimated 24 people/sq
mi living in and near the Crawford Area
population in 2000 (GSRSC 2005).
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Montrose County contains the
southeastern 75 percent of the current
range of the Crawford population. The
county was identified as one of the
fastest growing counties in the country,
with human population expected to
double from 2000–2030 (CDLA 2004)
and housing expected to increase by 68
percent by 2020. Growth will likely
fragment and destroy current habitat
and potential linkages to the San Miguel
population (GSRSC 2005), creating
further isolation of this population (see
Factor E for further discussion). The
northwestern 25 percent of the current
range is in Delta County, which is
projected to increase in population by
79 percent by 2030 (CDLA 2004) with
an increase in housing of 58 percent by
2020 (GSRSC 2005).
Human population growth and
housing development is occurring in all
of the Gunnison sage-grouse
populations and is projected to continue
to do so over the next 2 decades. Some
populations (Gunnison and Crawford)
have public lands as potential buffers
for the anticipated human population
growth. Additionally, with the
˜
exception of the Pinon Mesa population,
projected human population densities
in all sage-grouse populations are low
and do not appear to pose a significant
˜
threat. At Pinon Mesa, the threat of
development may be diminished by
current conservation easements with
additional easements planned.
Energy Development
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 and electrical
facilities (Connelly et al. 2004). Surveys
for recoverable resources occur
primarily through seismic activities,
using vibroesis trucks or shothole
explosives. Well pads vary in size from
0.10 ha (0.25 ac) for coalbed natural gas
wells in areas of level topography to
greater than 7 ha (17 ac) for deep gas
wells (Connelly et al. 2004). Pads for
compressor stations require 5–7 ha (12–
17 ac) (Connelly et al. 2004). Well
densities and spacing are typically
designed to maximize recovery of the
resource and are administered by State
agencies (Connelly et al. 2004). Well
densities and spacing on Federal lands
are governed by land management plans
which include resource analysis and
mitigation requirements. All the sage
grouse are considered species of special
concern and effects on grouse and
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habitat are part of the considerations for
permit conditions imposed by the BLM.
Direct habitat losses result from
construction of well pads, roads,
pipelines, powerlines, and the crushing
of vegetation during seismic surveys. As
disturbed areas are reclaimed, sagegrouse may repopulate the area.
However, re-population may take 20–30
years, as habitat conditions are not
immediately restored (Braun 1998). For
most developments, return to predisturbance population levels is not
expected due to a net loss and
fragmentation of habitat (Braun et al.
2002). After 20 years, sage-grouse have
not recovered to pre-development
numbers in Alberta, even though well
pads in these areas have been reclaimed
(Braun et al. 2002). In some reclaimed
areas, sage-grouse have not returned
(Aldridge and Brigham 2003). However
in Jackson County, Colorado, sagegrouse have repopulated, although not
to the pre-development levels.
Noise can drive away wildlife, cause
physiological stress, and interfere with
auditory cues and intraspecific
communication, as discussed
previously. Aldridge and Brigham
(2003) reported that, in the absence of
stipulations to minimize the effects,
mechanical activities at well sites may
disrupt sage-grouse breeding and
nesting activities. Greater sage-grouse
hens that bred on leks within 3 km (2
mi) of oil and gas development in the
upper Green River Basin of Wyoming
selected nest sites with higher total
shrub canopy cover and average live
sagebrush height than hens nesting
away from disturbance (Lyon 2000). The
author hypothesized that exposure to
road noise associated with oil and gas
drilling may have been one cause for the
difference in habitat selection. However,
noise could not be separated from the
potential effects of increased predation
resulting from the presence of a new
road. Above-ground noise is typically
not regulated to mitigate effects to sagegrouse or other wildlife (Connelly et al.
2004). Gunnison sage-grouse were
observed flushing from a lek when a
compressor station switched on,
disrupting breeding behavior (Jim
Garner, CDOW, pers. comm. 2004).
However, this was a single incident, and
we have no information to conclude that
noise from energy development poses a
significant threat to the species.
Water quality and quantity may be
affected in oil and gas development
areas. However, since, sage-grouse do
not require free water (Schroeder et al.
1999) we anticipate that impacts to
water quality from mining activities
would have minimal effects on them.
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Increased human presence resulting
from oil and gas development also can
impact sage-grouse either through
avoidance of suitable habitat, disruption
of breeding activities, or increased
hunting and poaching pressure
(Aldridge and Brigham 2003; Braun et
al. 2002; BLM 2003). Sage-grouse also
may be at increased risk for collision
with vehicles simply due to the
increased traffic associated with oil and
gas activities (BLM 2003).
Only a few studies have examined the
effects of oil and gas development on
sage-grouse. While each of these studies
reported sage-grouse population
declines, specific causes for the negative
impacts were not determined. In
Alberta, Canada, the development of
well pads and associated roads in the
mid-1980s resulted in the abandonment
of three greater sage-grouse lek
complexes within 200 m (656 ft) of
these features (Braun et al. 2002). Those
leks have not been active since that
time. A fourth lek complex has gone
from three to one lek with fewer
numbers of sage-grouse on it (Braun et
al. 2002). The well pads have since been
reclaimed, but greater sage-grouse
numbers have not recovered (we do not
have information on post-reclamation
vegetation). Subsequent to the
development of the Manyberries Oil
Field in high quality greater sage-grouse
habitat in Alberta, male sage-grouse
counts fell to the lowest known level
(Braun et al. 2002). Two additional leks
were directly disturbed, and neither of
these leks has been active within the
past 10 years (Braun et al. 2002). The
development of oil reserves in Jackson
County, Colorado, was concurrent with
decline of greater sage-grouse numbers
in the oil field area (Braun 1998). Sagegrouse populations still occur in at least
one long-term oil field development in
Colorado where leks are not within lineof-sight of an active well or powerline
(Braun et al. 2002). Although the
number of active leks has declined in
this field, sage-grouse have been
consistently documented there since
1973.
Of particular relevance to estimating
oil and gas development impacts is the
fidelity of sage-grouse hens to nesting
and summer brood-rearing areas
demonstrated by Lyon and Anderson
(2003). Hens that have successfully
nested will return to the same areas to
nest every year. If these habitats are
affected by oil and gas development,
there is a strong potential that
previously successful hens will return
but not initiate nesting (Lyon 2000).
Depending on the number of hens
affected, local populations could
decline.
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The reauthorization of the Energy
Policy and Conservation Act in 2000
dictated reinventory of Federal oil and
gas reserves, which identified extensive
reserves in the Greater Green River
Basin of Colorado, Utah, and Wyoming,
and the San Juan Basin of New Mexico
and Colorado (Connelly et al. 2004).
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) 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 8 out of 64
in counties producing natural gas in
2002 (Colorado Oil and Gas
Conservation Commission 2004).
In the current sage-grouse range in the
Gunnison Basin, 33 percent of the area
ranked as low potential with the
remainder having no potential for oil
and gas development (BLM 1999;
GSRSC 2005). No federally-leased lands
exist within the population area (BLM,
unpubl. lit. 2005f). However, one active
well and six inactive wells are on nonFederal lands in the current range in the
northern part of the Gunnison Basin
(BLM, unpubl. lit. 2005f).
The entire San Miguel Basin
population area is classified as having
high potential for oil and gas
development (BLM 1999; GSRSC 2005)).
Natural gas exploration in the San
Miguel Basin has increased in recent
months (CDOW, unpubl. lit. 2005g),
with 49 percent of the current range on
public and private land with Federal
leases for gas development (BLM,
unpubl. lit. 2005f). As a general
practice, all currently unleased BLM
lands within the current sage-grouse
range in the San Miguel Basin are being
deferred for oil and gas leasing until
completion of the Resource
Management Plans (RMPs) covering the
habitat for this population (anticipated
in 2007 and 2008).
The Colorado State Land Board
(CSLB) offered four sections of State
school section land for oil and gas
leasing in the San Miguel Basin
population in February 2006. One of
these is in occupied habitat of the
Miramonte Reservoir group and the
other three are in the Dry Creek Basin
group. The San Miguel County Board of
Commissioners requested that they
withdraw those sections or at least place
a ‘‘no surface occupancy’’ prescription
on the land with adherence to
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conservation measures in the RCP (San
Miguel County, unpubl. lit. 2006). The
CSLB stipulated that well pads would
be placed out of Gunnison sage-grouse
habitat [to the extent possible] on one
parcel in Dry Creek Basin where the
surface and the mineral rights are
owned by the CSLB (Linda Luther, San
Miguel County, pers. comm. 2006).
However, the other three parcels are
split estate (private surface, CSLBowned minerals) and the CSLB was
unwilling to, or believed they could not,
put stipulations for sage-grouse on those
parcels. San Miguel County will
continue to work with the landowners,
CSLB, and oil and gas companies to
place stipulations on the parcels (Linda
Luther, San Miguel County, pers. comm.
2006) but whether stipulations will
occur is uncertain. Nonetheless, this
illustrates a strong conservation
commitment by the County for the San
Miguel Basin population.
One oil and gas operator, who holds
several leases in the San Miguel Basin,
has decided to temporarily abandon
drilling on its leases in the Hamilton
Mesa, Miramonte Reservoir, Gurley
Reservoir, Beaver Mesa, and Iron
Springs Mesa areas because they are not
expected to be economically feasible.
However, exploration and production
may continue in the future (CDOW,
unpubl. lit. 2005g). Fifty-one oil and gas
wells have been developed in the
current range in the San Miguel Basin.
All but 1 is in the Dry Creek Basin and
47 are on federally-leased land (BLM,
unpubl. lit. 2005f). Additional wells on
existing leases are proposed for this area
in the next 10 years. Five gas pipelines
are proposed for this development, one
of which is expected to transect winter
habitat and another will remove habitat
in places (BLM, unpubl. lit. 2005g). 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, unpubl. lit. 2005g).
The Monticello group is in an area of
high energy potential (GSRSC 2005). Oil
and gas leases with State and Federal
mineral rights have been acquired or
applied for on over 2,000 ha (5,000 ac)
(6 percent) in the current range (Tammy
Wallace, BLM, pers. comm. 2005). One
new well pad was constructed in 2005
(San Juan County GSWG, unpubl. lit.
2005) and additional drilling is
expected to occur in the next few years.
However, BLM is currently deferring
new leases in the current range.
No oil and gas wells are within the
current range in the Pinon Mesa area,
although oil and gas leases occupy 17
percent of this habitat (BLM, unpubl. lit.
2005f). The remaining portion of the
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current range has no potential for oil or
gas in this area except for a small
portion on the eastern edge of the largest
habitat block (BLM 1999; GSRSC 2005).
The Crawford population is in an area
with high to medium potential for oil
and gas development (BLM 1999;
GSRSC 2005). However, no Federal
leases and only one well (on nonFederal lease property) are in the
current range (BLM, unpubl. lit. 2005f).
The BLM has deferred Federal oil and
gas leases in the current range in this
population until resource management
plans addressing Gunnison Sage Grouse
are adopted. Future development could
occur on State and private land in the
Crawford area under Colorado Oil and
Gas Commission regulation and on BLM
land if their future RMP allows it.
In summary, some Gunnison sagegrouse habitat is in areas with high
potential for oil and gas development,
particularly in the San Miguel Basin. A
few studies on greater sage-grouse
reported population declines in
response to oil and gas development
(Braun et al. 2002; Lyon and Anderson
2003), although specific causes for the
declines were not determined. A recent
study of greater sage-grouse in Wyoming
found that as oil and gas development
increased (Holloran 2005). Negative
impacts to active leks extended to a
distance of 5 km (3 mi) from an active
drilling rig. Similarly, juvenile male
recruitment to impacted leks also fell.
Nesting females avoided areas with high
well densities, although site fidelity to
previous nesting locations may result in
delayed population response to the
habitat changes associated with
development. While some birds were
displaced by the disturbance, Holloran
(2005) also found that many sage-grouse
discontinued breeding attempts, and
others died at a higher rate than birds
from unaffected areas. He concluded
that natural gas field development
contributes to localized greater sagegrouse extirpations, but that regional
populations levels, although negatively
impacted, are not as severely
influenced.
Application of these impacts from gas
development to the San Miguel and
Crawford populations and Monticello
group could threaten their long-term
persistence. However, the immediate
threat to Gunnison sage-grouse is
curtailed by BLM lease deferments.
Additionally, available information
suggests that economic infeasibility of
extraction will act to minimize the
likelihood this development will occur
at a significant enough level to imperil
Gunnison sage-grouse.
Colorado has been the largest
producer of coalbed methane in the
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country since 2002, and production has
increased (Cappa et al. 2005). Deposits
exist under the current range of the San
Miguel and Crawford populations
(Cappa et al. 2005), although no wells
have been drilled to date in those areas
(D. Spencer, BLM, pers. comm. 2005)
leading us to believe this does not
represent a significant threat to these
populations and therefore to the species.
Renewable energy resources, such as
windpower, require many of the same
features for construction and operation
as do nonrenewable energy resources.
Therefore, we anticipate that potential
impacts from direct habitat losses,
habitat fragmentation through roads and
powerlines, noise, and increased human
presence (Connelly et al. 2004) will
generally be the same as already
discussed for nonrenewable energy
development. Windpower may have
additional mortalities resulting from
sage-grouse flying into turbine rotors or
meteorological towers (Erickson et al.
2001), although the magnitude of such
losses is unquantified. One greater sagegrouse was found dead within 45 m
(148 ft) of a turbine on the Foote Creek
Rim wind facility in south-central
Wyoming, presumably from flying into
a turbine (Young et al. 2003). During 3
years of monitoring operation, this is the
only known sage-grouse mortality at this
facility.
Current interest and speculation in
wind energy exists in the Monticello
area. A wind test tower (anemometer)
has been erected at a site approximately
2.4 km (1.5 mi) from a lek (GSRSC
2005), and landowners in the area have
been contacted by power company
contractors about leases for wind power
development. If wind turbines are
placed near leks and other important
habitat in the Monticello group,
depending on the location and number
of turbines, Gunnison sage-grouse in
this area may be affected. We are not
aware of any other wind energy
development proposed throughout the
rest of the Gunnison sage-grouse current
range. We have no evidence that current
or future wind energy development
threatens or endangers the long-term
persistence of the species.
Mining
Surface mining for any mineral
resource (coal, uranium, copper,
bentonite, gypsum, oil shale, phosphate,
limestone, gravel, etc.) will result in
direct habitat loss for Gunnison sagegrouse if the mining occurs in current
sagebrush range. Direct loss of sagegrouse habitat also can occur if the
overburden and/or topsoil resulting
from mining activities are stored in
sagebrush habitats. The actual effect of
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this loss depends on the quality,
amount, and type of habitat disturbed,
the scale of the disturbance, and the
availability of adjacent habitats (Proctor
et al. 1983; Remington and Braun 1991).
Regulation of non-coal mining in the
United States is at the discretion of the
individual States. New vegetation types
including exotic species may become
established on mined areas (Moore and
Mills 1977), altering their suitability for
sage-grouse. If reclamation plans call for
the permanent conversion of the mined
area to a different habitat type (e.g.,
agriculture) the habitat loss becomes
permanent. Invasive exotic plants also
may establish on the disturbed surfaces.
Removal of the overburden and target
mineral may result in changes in
topography, subsequently resulting in
changes in microclimates and
microhabitats (Moore and Mills 1977).
Additional habitat losses can occur if
supporting infrastructure, such as roads,
railroads, utility corridors, buildings,
etc., become permanent landscape
features after mining and reclamation
are completed (Moore and Mills 1977),
which is allowed in Colorado (Colorado
Statute Title 34, Article 32) and Utah
(R647–4–110).
Other indirect effects from mining can
include reduced air quality from
fugitive dust, degradation of surface
water quality and quantity, disturbance
from noise, human presence, and
mortality from collision with mining
equipment (Moore and Mills 1977;
Brown and Clayton 2004). Fugitive dust
could affect local vegetative and insect
resources (Moore and Mills 1977). Most
large surface mines are required to
control fugitive dust, so these impacts
are probably limited.
Since sage-grouse do not require free
water (Schroeder et al. 1999), we
anticipate that impacts to water quality
from mining activities would have
minimal population-level effects. The
possible exception is degradation or loss
of riparian areas, which could result in
brood habitat loss. The effects on sagegrouse of noise from mining are
unknown, but sage-grouse also depend
on acoustical signals to attract females
to leks (Gibson and Bradbury 1985;
Gratson 1993). If noise does interfere
with mating display and thereby female
attendance, younger males will not
attend the lek, and eventually leks will
become inactive (Amstrup and Phillips
1977; Braun 1986). Mining also can
impact sage-grouse through the
increased presence of human activity,
either through avoidance of suitable
habitat adjacent to mines or through
collisions with vehicles associated with
mining operations (Moore and Mills
1977; Brown and Clayton 2004).
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However, we were unable to find any
information regarding increased
mortality of Gunnison sage-grouse as a
result of this effect.
Within Gunnison sage-grouse current
range, coal, uranium, and vanadium are
the most commonly mined minerals and
have begun to attract increased interest
in recent years (Cappa et al. 2005).
These minerals were mined historically
in the San Miguel area and affected an
unknown amount of the historical range
of the Gunnison sage-grouse. Uranium
deposits are within the current range of
the San Miguel Basin population and
Monticello group (Coker 2001; Cappa et
al. 2005) and three mines near the San
Miguel Basin population were reopened
in 2004 (Cappa et al. 2005). Due to the
exploratory nature of this mineral
activity to date and the somewhat
speculative nature of its occurrence in
the future, we do not believe that this
activity will be a significant threat to the
species in the foreseeable future.
Six active hardrock, gravel or road fill
mines are located on BLM land in sagegrouse habitat in the Gunnison Basin
(BLM, unpubl. lit. 2005c). Total
disturbance, excluding roads, is 39 ha
(96 ac). Two hundred ninety-one
inactive or abandoned mines and
numerous miles of roads have caused
unquantified past habitat loss and
fragmentation (BLM, unpubl. lit. 2005b),
but future impact of hardrock, gravel, or
road fill mines are likely limited.
We conclude that present and future
mining activities appear to be limited
and do not pose a significant threat to
Gunnison sage-grouse.
Grazing
Grazing is the dominant use of
sagebrush rangelands in the West
(Connelly et al. 2004); almost all
sagebrush areas are managed for
livestock grazing (Knick et al. 2003).
Although we lack information on the
proportion of occupied Gunnison sagegrouse habitat that is grazed, we expect
that it is a vast majority. Excessive
grazing by domestic livestock during the
late 1800s and early 1900s, along with
severe drought, significantly affected
sagebrush ecosystems (Knick et al.
2003). Although current livestock
stocking rates are substantially lower
than high historical levels (Laycock et
al. 1996), long-term effects from this
overgrazing, including changes in plant
communities and soils, persist today.
Although it is likely that livestock
grazing and associated land treatments
have altered plant composition,
increased topsoil loss, and increased
spread of exotic plants, the impacts on
sage-grouse are not clear. Few studies
have directly addressed the effect of
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livestock grazing on sage-grouse (Beck
and Mitchell 2000; Wamboldt et al.
2002; Crawford et al. 2004), and there is
little direct experimental evidence
linking grazing practices to sage-grouse
population levels (Braun 1987, Connelly
and Braun 1997). Rowland (2004)
conducted a literature review and found
no experimental research that
demonstrates grazing alone is
responsible for reduction in sage-grouse
numbers.
The GSRSC (2005) could not find a
direct correlation between historic
grazing and reduced sage-grouse
numbers. It has been demonstrated that
the reduction of grass heights due to
livestock grazing of sage-grouse nesting
and brood-rearing habitat negatively
affects nesting success by reducing
cover necessary for predator avoidance
(Gregg et al. 1994; Delong et al. 1995;
Connelly et al. 2000a). Nest success in
Gunnison sage-grouse habitat is related
to greater grass and forb height and
shrub density (Young 1994). In addition,
livestock consumption of forbs may
reduce food availability for sage-grouse.
This is particularly important for prelaying hens, as forbs provide essential
calcium, phosphorus, and protein. A
hen’s nutritional condition affects nest
initiation rate, clutch size, and
subsequent reproductive success
(Connelly et al. 2000a). Livestock
grazing can reduce the forage
availability in breeding and broodrearing habitat, with possible
subsequent negative effects on sagegrouse populations (Braun 1987; Young
1994; Dobkin 1995; Beck and Mitchell
2000). Exclosure studies have
demonstrated that domestic livestock
grazing also reduces water infiltration
rates and cover of herbaceous plants and
litter, as well as compacting soils and
increasing soil erosion (Braun 1998).
This results in a change in the
proportion of shrub, grass, and forb
components in the affected area, and an
increased invasion of exotic plant
species that do not provide suitable
habitat for sage-grouse (Miller and
Eddleman 2000). Hulet (1983, as cited
in Connelly et al. 2000a) found that
heavy grazing could lead to increases in
ground squirrel numbers; ground
squirrel depredate sage-grouse nests.
Thus, livestock stocking levels and
season and duration of use are
important factors of livestock operations
related to impacts on sage-grouse
include
Other consequences of grazing
include several related to livestock
trampling. Outright nest destruction by
livestock trampling does occur, and the
presence of livestock can cause sagegrouse to abandon their nests
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(Rasmussen and Griner 1938; Patterson
1952; Call and Maser 1985; Crawford et
al. 2004). Call and Maser (1985) indicate
that forced movements of cattle and
sheep could have significant effects on
nesting hens and young broods caught
in the path of these drives. Livestock
also may trample sagebrush seedlings
thereby removing a source of future
sage-grouse food and cover (Connelly et
al. 2000a), and trampling of soil by
livestock can reduce or eliminate
biological soil crusts making these areas
susceptible to cheatgrass invasion (Mack
1981 as cited in Miller and Eddleman
2000; Young and Allen 1997; Forman
and Alexander 1998).
Livestock grazing also may compete
directly with sage-grouse for rangeland
resources. Aldridge and Brigham (2003)
suggest that poor livestock management
in mesic sites results in a reduction of
forbs and grasses available to greater
sage-grouse chicks, thereby affecting
chick survival. The effects of direct
competition between livestock and sagegrouse depend on condition of the
habitat and grazing practices.
Development of springs and other
water sources to support livestock in
upland shrub-steppe habitats can
artificially concentrate domestic and
wild ungulates in important sage-grouse
habitats, thereby exacerbating grazing
impacts in those areas through
vegetation trampling, etc. (Braun 1998).
Diverting water sources has the
secondary effect of changing the habitat
present at the water source before
diversion. This could result in the loss
of either riparian or wet meadow habitat
important to sage-grouse as sources of
forbs or insects.
Sagebrush removal to increase
herbaceous forage and grasses for
domestic and wild ungulates is a
common practice in sagebrush
ecosystems (Connelly et al. 2004).
Herbicide, especially Tebuthiuron
applications were commonly used to
kill large expanses of sagebrush, but it
also killed many forbs used for broodrearing (Crawford et al. 2004). Thinning,
rather than removal, of sagebrush using
Tebuthiuron has been the focus of some
treatments (Emmerich 1985; Olson and
Whitson 2002).
Sage-grouse response to herbicide
treatments depends on the extent to
which forbs and sagebrush are killed.
Chemical control of sagebrush has
resulted in declines of sage-grouse
breeding populations through the loss of
live sagebrush cover (Connelly et al.
2000a). Herbicide treatment also can
result in sage-grouse emigration from
affected areas (Connelly et al. 2000a),
and has been documented to have a
negative effect on nesting, brood
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carrying capacity (Klebenow 1970), and
winter shrub cover essential for food
and thermal cover (Pyrah 1972 and
Higby 1969 as cited in Connelly et al.
2000a). Carr and Glover (1970) found
that greater sage-grouse would use
block-sprayed areas for strutting but not
for other activities. They found that
adults would move the 1.6 km (1.0 mi)
across the sprayed areas but believed
that movement across the area may
cease as dead standing sagebrush
deteriorated. They also determined that
broods were impeded from moving to a
previously used riparian area due to
killing of the sagebrush between nesting
sites and the riparian area. Winter use
also did not occur in the area due to
lack of live sagebrush for forage.
Small treatments interspersed with
non-treated sagebrush habitats did not
affect sage-grouse use, presumably due
to minimal effects on food or cover
(Braun 1998). Also, application of
herbicides in early spring to reduce
sagebrush cover may enhance some
brood-rearing habitats by increasing the
coverage of herbaceous plant foods
(Autenrieth 1981).
Mechanical treatments are designed to
either remove the above-ground portion
of the sagebrush plant (mowing, roller
chopping, and rotobeating), or to uproot
the plant from the soil (grubbing,
bulldozing, anchor chaining, cabling,
railing, raking, and plowing; Connelly et
al. 2004). These treatments were begun
in the 1930s and continued at relatively
low levels to the late 1990s (Braun
1998). Mechanical treatments, if
carefully designed and executed, can be
beneficial to sage-grouse by improving
herbaceous cover, improving forb
production, and resprouting sagebrush
(Braun 1998). However, adverse effects
also have been documented (Connelly et
al. 2000a). Mechanical treatments in
blocks greater than 100 ha (247 ac), or
of any size seeded with exotic grasses,
degrade sage-grouse habitat by altering
the structure and composition of the
vegetative community (Braun 1998).
For Gunnison sage-grouse, the best
measure of potential grazing impacts is
derived from monitoring habitat
conditions in grazing allotments and
comparing that information to grouse
habitat objectives. BLM developed
habitat objectives for Gunnison sagegrouse from habitat objectives in each of
the local conservation plans. They are
similar to the grazing management
guidelines that were later developed for
the RCP (GSRSC 2005). Where
information is available, the comparison
between BLM’s habitat conditions and
habitat objectives is presented below.
Within the current range in the
Gunnison Basin, 23 of 66 BLM grazing
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allotments have sage-grouse habitat
objectives incorporated into the
allotment management plans or Records
of Decision for permit renewals (BLM,
unpubl. lit. 2005h). In 2002, 50 percent
of the Wyoming big sagebrush/Indian
ricegrass (Achnathrum hymenoides)
vegetation, which accounts for a
significant portion of the nesting/early
brood-rearing habitat, met the desired
condition on BLM lands in the area
(GSRSC 2005). In 2003, 75 percent of
32,000 ha (80,000 ac) of nesting/early
brood-rearing habitat monitored met
habitat objectives (BLM, unpubl. lit.
2004). Under 50 percent of the 579 km
(360 mi) of riparian areas, which are
important for brood-rearing, met desired
conditions identified in the Gunnison
Basin Conservation Plan (1997) and 85
percent met short-term stubble height
objectives (nesting cover) (BLM, unpubl.
lit. 2004). In 2004, 23,000 ha (56,000 ac)
were monitored within a 3-km (2-mi)
radius of a lek, and less than 2 percent
met the local (Gunnison Basin
Conservation Plan 1997) objectives for
grass stubble height (BLM, unpubl. lit.
2005i). However, grass growth may have
been suppressed by effects of drought,
which appeared to be impacting habitat
in most populations in 2004 (See Factor
E for further drought discussion).
We were able to acquire information
on grazing intensity for only the Dry
Creek Basin group of the San Miguel
Basin population. No sage-grouse
habitat objectives or conservation
measures are in allotment management
plans or grazing permits for BLM
allotments in that area (BLM, unpubl.
lit. 2005d and 2005g). Sagebrush
patches there continue to succeed to a
late-seral sagebrush community lacking
in understory.
Eight BLM grazing allotments totaling
2,700 ha (6,700 ac) occur within the
current range in the Monticello group
(San Juan County GSWG, unpubl. lit.
2005). Few or no habitat objectives have
been incorporated into BLM allotment
management plans, nor have changes in
grazing intensity been implemented for
sage-grouse in the group. No data are
available on whether grazing lands on
BLM or private land are meeting sagegrouse habitat objectives for the
Monticello group. The CRP has
provided a considerable amount of
brood-rearing habitat in the Monticello
group because of its forb component.
Grazing of CRP in Utah occurred in
2002 under emergency Farm Bill
provisions due to drought. Radiocollared males and non-brood-rearing
females exhibited temporary avoidance
of grazed fields during and after grazing
(San Juan County GSWG, unpubl. lit.
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2005), although one hen with a brood
continued to use a grazed CRP field.
Fifty grazing allotments on BLM land
are within the current range in the
˜
Pinon Mesa population (BLM, unpubl.
lit. 2005a). We do not know the extent
of grazing on the private land within the
˜
Pinon Mesa sage-grouse range. Only
three BLM allotments (6 percent) have
Gunnison sage-grouse habitat objectives
incorporated into the allotment
management plan or grazing permit in
this area. We have no information on
habitat conditions in any of the
allotments in the population area.
In the Crawford population there are
nine BLM grazing allotments, totaling
about 8,500 ha (21,000 ac) or 60 percent
of the habitat. Sage-grouse conservation
measures have been incorporated into
seven of the allotment plans. On BLM
land in the Crawford population,
Animal Unit Months have been reduced
and grazing management was recently
changed (BLM unpubl. lit. 2005d). The
Gunnison Gorge Land Health
Assessment showed that 34,000 out of
44,000 ha (84,000 out of 110,000 ac), or
76 percent of the current range, met the
land health standard for threatened and
endangered species (including
Gunnison sage-grouse habitat). The
extent of livestock grazing on private
land is unknown.
In conclusion, habitat manipulations
to improve livestock forage can affect
sage-grouse habitat. In the Gunnison
Basin, BLM habitat conditions are
adequate for approximately 50 to 75
percent of the area measured, depending
on the parameters and year they were
measured. The Gunnison Basin
population has been stable over time
(see Table 2 and Garton 2005),
suggesting that grazing is not negatively
affecting the population in this area. In
the Crawford area 76 percent of the
current range met standards, so we do
not consider grazing to be a threat there.
Although we do not have specific
information on the remaining BLM
lands, it is reasonable to assume similar
conditions exist on the remainder of the
BLM lands. In the Monticello area,
private lands enrolled in CRP are
usually left ungrazed. We lack data on
the extent of private land grazing on
Gunnison Sage-Grouse habitat in the
remainder of its range. However, based
on the data available to us, we conclude
that there is insufficient data that
demonstrates grazing is a threat to the
species.
We lack adequate information on the
effect of deer and elk grazing on
Gunnison sage-grouse and their habitat
to fully address this potential impact.
Overgrazing by deer and elk may cause
local degradation of habitats by removal
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of forage and residual hiding and
nesting cover. Hobbs et al. (1996)
documented a decline in available
perennial grasses as elk densities
increased. Such grazing could
negatively impact nesting cover for sagegrouse. Excessive but localized deer and
elk grazing has been documented in the
Gunnison Basin (BLM, unpubl. lit.
2005i; Paul Jones, CDOW, pers. comm.
2005). The winter range of deer and elk
overlaps the year-round range of the
Gunnison sage-grouse. Deer and elk
herds were above the carrying capacity
of their winter range before the 2002
drought and were not significantly
reduced during or after (BLM, unpubl.
lit. 2005i). However, no evidence exists
that competition for resources is
limiting Gunnison sage-grouse in the
Gunnison Basin. Although grazing by
deer and elk occurs in all population
areas, information on overgrazing by
deer or elk and its potential effect on
other populations has not been reported.
Invasive Weeds
Invasive species have been defined as
those that are not native to an ecosystem
and whose introduction causes, or is
likely to cause, economic or
environmental harm or harm to human
health (Executive Order 13112, 1999).
Invasive species often cause declines in
native plant populations by reducing
light, water, and nutrients, and they
grow so quickly that they outcompete
other species (Wooten et al. 1996).
Exotic plants can reduce and eliminate
populations of plants that sage-grouse
use for food and cover. Frequent fires
with short intervals within sagebrush
habitats favor invasion of cheatgrass,
which is unsuitable as sage-grouse
habitat (Schroeder et al. 1999).
Cheatgrass then shortens the fire
interval (from approximately 30 years
down to 5 years), perpetuating its own
persistence and spread, and
exacerbating the effects of fire in
remaining sage-grouse habitats
(Whisenant 1990; Billings 1994;
Grahame and Sisk 2002; Connelly et al.
2004). A cheatgrass invasion into
sagebrush habitat can lead to an
eventual conversion of sagebrush/
perennial grass community to
sagebrush/annual grass or annual grass
rangeland (Connelly et al. 2000a; Miller
and Eddleman 2000). Rehabilitation of
an area to sagebrush after cheatgrass
becomes established is extremely
difficult (Connelly et al. 2004). In some
cases cheatgrass invasion encourages
other exotic species such as knapweed
and thistle (Grahame and Sisk 2002).
Cheatgrass has invaded areas in
Gunnison sage-grouse range,
supplanting sagebrush habitat. Connelly
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et al. (2000a) indicated that some greater
sage-grouse populations have been
affected and some will decline due to
projected, continuing spread of
cheatgrass domination in the absence of
effective management. There has not
been a demonstrated change in fire
cycle in any population of Gunnison
sage-grouse, so they may not be as
threatened as greater sage-grouse. While
all of the Colorado Gunnison sagegrouse counties have noxious weed
programs, none identify cheatgrass as a
noxious weed for control purposes
(Colorado Department of Agriculture
2003). The BLM, on whose land many
acres of cheatgrass occur, is currently
restricted to application of 6 ha (15 ac)
of an effective herbicide per Field Office
per year, limiting their ability to control
this noxious weed (BLM, unpubl. lit.
2005i).
Approximately 14,249 ha (35,200 ac)
have been invaded by cheatgrass in the
Gunnison Basin, equaling 6 percent of
the current range (BLM, unpubl. lit.
2005i) with 405 ha (1,000 ac) considered
dominated by cheatgrass (Sandy
Borthwick, BLM, pers. comm. 2005)
despite past treatments to control this
weed (Gunnison Watershed Noxious
Weed Program, unpubl. lit. 2005). In
addition, cheatgrass has been found at
50 other locations and 21 roads or road
segments throughout the Gunnison
Basin population’s range. Although
disturbed areas contain the most weeds,
they can readily spread into
undisturbed habitat. Given its invasive
nature, cheatgrass may increase in the
Gunnison Basin in the future, but the
actual extent or rate of increase is
uncertain. Cheatgrass is present
throughout much of the current range in
the San Miguel Basin (BLM, unpubl. lit.
2005d). It is sparsely scattered in the
five Gunnison sage-grouse groups east of
Dry Creek Basin, which are at higher
elevation, and does not appear to pose
a serious threat to them (CDOW,
unpubl. lit. 2005g). Because cheatgrass
can readily dominate native plant
communities at lower elevations
(CDOW, unpubl. lit. 2005g), it may
affect the Dry Creek Basin group, which
comprises 62 percent of the San Miguel
Basin population. Invasive species are
present at low levels in the Monticello
groups (San Juan County GSGWG,
unpubl. lit. 2005). 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 Pinon Mesa
population (R. Lambeth, BLM, pers.
comm. 2005). It occurs in the lower
˜
elevation areas below Pinon Mesa that
were formerly Gunnison sage-grouse
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19971
sagebrush seed. Where sagebrush
habitat has become fragmented and
limited, there is potential for fire to
eliminate the existing seed source,
reducing the likelihood of natural
regeneration.
A variety of techniques have been
attempted at re-establishing sagebrush
post-fire, with mixed success (Quinney
et al. 1996, Livingston 1998).
Restoration of the sagebrush biome
following a fire has been complicated
not only by the invasion of exotic
annual plant species, but the difficulty
associated with establishing sagebrush
seedlings (Boltz 1994). Wirth and Pyke
(2003) reported that forb response postfire is dependant on the forb community
pre-burn.
A clear positive response of sagegrouse to fire has not been demonstrated
(Braun 1998). A number of studies have
found adverse effects to sage grouse
populations resulting from fire. (Call
and Maser 1985; Rowland and Wisdom
2002; Nelle et al. 2000; Byrne 2002;
Fire and Fire Management
Connelly et al. 2000c; Fischer et al.
There have been significant changes
1996a). However, Klebenow (1970),
in fire frequency, distribution, and
Gates (1983, as cited in Connelly et al.
intensity since European settlement
2000c), Sime (1991 as cited in Connelly
(Young et al. 1979; Miller and Eddleman et al. 2000a), and Pyle and Crawford
2000). The effects of fire on sagebrush
(1996) all indicated that fire could
habitats vary according to the species
improve brood-rearing habitat.
and subspecies of sagebrush and other
Three prescribed burns have occurred
plant species present (e.g., the
in the Gunnison Basin since 1984,
understory) and the frequency, size and totaling 700 ha (1,700 ac). The fires
intensity of fires. Widely variable
created large sagebrush-free areas that
estimates of mean fire intervals have
were further degraded by poor post-burn
been described in the literature—35–100 livestock management (BLM, unpubl.
years (Brown 2000), greater than 50
lit. 2005i). Two prescribed burns
years for big sagebrush communities
conducted in 1986 (105 ha (260 ac)) and
(McArthur 1994), 12–15 years for
1992 (140 ha (350 ac)) on BLM land in
mountain big sagebrush (Artemesia
the San Miguel Basin on the north side
tridentata vaseyana) (Miller and Rose
of Dry Creek Basin had negative impacts
1999), 20–100 years (Peters and Bunting on sage-grouse. The burns were
1994), 10–110 years depending on
conducted for big game forage
sagebrush species or subspecies and
improvement, but Land Health
specific geographic area (Kilpatrick
Assessments in 2004, noted that
2000), and 13–25 years (Frost 1998 cited sagebrush had died and largely been
in Connelly et al. 2004).
replaced with weeds (BLM, unpubl. lit.
Fire tends to extensively reduce the
2005g). The 2002 Burn Canyon fire in
sagebrush component within the burned the Dry Creek Basin and Hamilton Mesa
areas. Time needed for most sagebrush
areas created a short-term habitat loss of
species and subspecies to reestablish
890 ha (2,200 ac). Fire has apparently
after burning suggests they evolved in
not occurred recently in the Monticello
an environment where wildfire was
group.
One wildfire in the Gunnison Basin
infrequent (interval of 30–50 years) and
burned 445 ha (1,098 ac) in June 2002
patchy in distribution (Braun 1998).
(Sandy Borthwick, BLM, pers. comm.
Prior to European settlement, fire
patterns in sagebrush communities were 2006). There appears to be a good
response to the fire from grass and forbs.
patchy, particularly in Wyoming big
sagebrush, due to the discontinuous and Mountain big sagebrush also appears to
limited fuels and unburned islands that have responded well based on seedling
establishment in seeded and non-seeded
remained after a fire (Miller and
Eddleman 2000). Huff and Smith (2000) areas. Some cheatgrass, suspected to
have come in with the sagebrush seed,
noted that these unburned islands
was observed on the seeded sites but
appear to be important to the future
was sparse (Sandy Borthwick, BLM,
recolonization of the sagebrush
pers. comm. 2006). At least four
community by providing sources of
range. It invaded two small prescribed
burns in or near occupied habitat
conducted in 1989 and 1998 (BLM,
unpubl. lit. 2005a), and continues to be
a concern with any ground disturbing
projects. Four invasive weedy forbs also
occur in the area, but occupy less than
4 ha (10 ac) (BLM, unpubl. lit. 2005a).
Invasive weeds, especially cheatgrass,
occur primarily along roads, other
disturbed areas, and isolated areas of
untreated vegetation in the Crawford
population. No current estimates of the
extent of weed invasion are available
(BLM, unpubl. lit. 2005d).
Although invasive weeds, especially
cheatgrass, have affected some sagegrouse habitat, the impacts do not
appear to be threatening individual
populations or the species rangewide.
We have no basis for expecting on the
potential spread of cheatgrass into sage
grass habitat, and we have not
information that suggests that it will be
a threat in the future.
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wildfires in the last 20 years burned
39,300 ha (97,200 ac) in the current
˜
range in the Pinon Mesa area and
created large expanses almost devoid of
sagebrush and invaded by cheatgrass
and Russian thistle (Salsola spp) (BLM,
unpubl. lit. 2005a). Some wildfire
suppression has occurred in sage-grouse
habitat in the vicinity of residences. Fire
occurs infrequently in the Crawford
area. The Fruitland wildfire burned 240
ha (600 ac) of pinyon-juniper and old
sagebrush in 1996. Two efforts to reseed
the area with sagebrush and native forbs
and grasses failed and the area is now
dominated by cheatgrass (BLM, unpubl.
lit. 2005d). Spread of cheatgrass into
other areas is an increasing threat due
to its establishment in the burned area.
Where fire suppression has occurred,
sagebrush communities may advance
successionally to pinyon pine and
juniper (Burkhardt and Tisdale 1969;
Young and Evans 1981; Miller and Rose
1995; Miller et al. 2000; Wrobleski and
Kauffman 2003), eventually resulting in
a near total loss of shrubs and sagegrouse habitat (Miller and Eddleman
2000). Gambel oak invasion as a result
of fire suppression also has been
identified as a potential threat to
Gunnison sage-grouse (CDOW, unpubl.
lit. 2002). Trees provide perches for
raptors; consequently, Gunnison sagegrouse avoid areas with pinyon-juniper
(Commons et al. 1999).
Native tree or shrub encroachment on
11,336 ha (28,000 ac) or 5 percent of the
current range has occurred in the
Gunnison Basin. Oakbrush
encroachment is a potential threat in the
San Miguel Basin, especially in the five
easterly and higher elevation groups.
Approximately 2,955 ha (7,300 ac) or 9
percent of the current range in these
areas are dominated by oakbrush.
Mountain shrubs also have encroached
on about 3,280 ha (8,100 ac) or 9 percent
of habitat in the San Miguel Basin
population (GSRSC 2005). No pinyonjuniper dominated areas are within the
current range.
The Monticello area has 1,170 ha
(2,889 ac) or 5 percent of the current
range dominated by oakbrush (GSRSC
2005). Pinyon and juniper trees are
reported to be encroaching throughout
the current range in the Monticello
group, based on a comparison of
historical versus current aerial photos,
but there has been no quantification or
mapping of the encroachment (San Juan
County GSWG, unpubl. lit. 2005). A
relatively recent invasion of pinyon and
juniper trees between the Dove Creek
and Monticello groups appears to be
contributing to their isolation from each
other (GSRSC 2005).
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Jkt 208001
About 1,600 ha (3,935 ac) of trees and
shrubs dominate 16 percent of the
˜
current range in the Pinon Mesa area
(GSRSC 2005). In addition to limiting
habitat, tree and shrub encroachment is
˜
further isolating Pinon Mesa from the
Crawford and San Miguel populations,
thereby impacting connectivity and
maintenance of genetic diversity (see
discussion under Factor E).
Approximately 9 percent of the 1,300 ha
(3,200 ac) of the current range in the
Crawford population is classified as
dominated by pinyon-juniper (GSRSC
2005). However, BLM (unpubl. lit.
2005d) estimates that as much as 20
percent of the population area is
occupied by pinyon-juniper. The
Crawford population also has about 400
ha (953 ac) or 3 percent of oakbrushdominated land in the current range
(GSRSC 2005).
Although fire suppression has likely
caused low to moderate levels of native
tree and shrub encroachment in the
populations we considered, none of the
encroachment is sufficient to pose a
significant threat to the Gunnison sagegrouse at a population or rangewide
level. Fires can cause spread of weeds
and burn suitable sage-grouse habitat,
but they do not threaten the species
currently and we do not anticipate that
they will in the future. Fires can be
beneficial by rejuvenating forbs and
grasses and reducing encroachment of
native trees and shrubs.
Conclusion for Factor A
Habitat fragmentation has affected the
exchange of individuals among
populations of Gunnison sage-grouse.
Population isolation is most
pronounced in Pinon Mesa and
Monticello. There also is some evidence
that the Monticello and Dove Creek
groups have recently been separated
from each other by habitat changes;
however, there is no evidence that
habitat fragmentation has limited
exchange of sage-grouse within other
populations, including the San Miguel
Basin population which has six groups
separated by 1–4 air miles.
Forty-three percent of the occupied
habitat in the Monticello group was
converted to agriculture in the past, but
little conversion is expected there in the
future. Other occupied population areas
have had lower percentages of past
conversions with no current or future
conversion expected. There is evidence
that Gunnison sage-grouse will not use
agricultural fields further than about 50
m (160 ft) from the edge for foraging but
no evidence that agricultural conversion
currently threatens the sage-grouse
rangewide. Reservoirs caused
fragmentation and/or loss of a small
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Fmt 4701
Sfmt 4700
percentage of habitat in the Gunnison
Basin population and the Gurley and
Miramonte groups in the San Miguel
Basin population. However, there is no
evidence that reservoir development has
caused range-wide or population-wide
threats to the Gunnison sage-grouse.
Other than two direct mortalities in
the San Miguel Basin population, we
were unable to find any data
substantiating effects of roads to impacts
on Gunnison sage-grouse populations.
Based on the stable population trend,
the current network of roads does not
appear to be a threat to the species, and
we have no information that indicates
that future road development will pose
a threat to the species rangewide.
Despite the presence of powerlines in
all populations there also is no evidence
that they are threatening Gunnison sagegrouse populations rangewide or within
populations.
Urban or exurban development does
not appear to be a threat to the sagegrouse based on the low human
population densities in all but one
county with Gunnison sage-grouse.
Projections of human population growth
and housing development are not
known to be a rangewide threat.
High potential for oil and gas
development only exists in the San
Miguel Basin population and Monticello
group; high to medium potential exists
in the Crawford population. Low or no
potential exists in the Gunnison Basin
and Pinon Mesa populations. Energy
development on Federal lands can
contain conservation measures for
wildlife species (see Factor D for a more
thorough discussion). We have no
evidence that oil and gas development
will threaten the Gunnison sage-grouse
rangewide in the foreseeable future.
Other energy development activities,
such as wind turbine development, are
not expected to cause a threat to the
Gunnison sage-grouse rangewide in the
foreseeable future. Additionally, coal or
hardrock mining appears to pose little
threat to occupied habitat.
Although overgrazing can affect
habitat, it is unclear whether effects
from current livestock grazing
management practices, such as
reduction of vegetation below suitable
conditions or spread of weeds threaten
the Gunnison sage-grouse at a
population or rangewide level.
Cheatgrass may impact sage-grouse
habitat in nearly all Gunnison sagegrouse populations. However, there has
not been a demonstrated change in fire
cycle in any population, nor is it
documented that cheatgrass, at its
current distribution and density, will
threaten the Gunnison sage-grouse in
the foreseeable future. Invasive weeds
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other than cheatgrass occur in some
populations but at levels that do not
cause a threat to the Gunnison sagegrouse.
Fires can cause spread of weeds and
burn suitable sage-grouse habitat, but
also may be beneficial by rejuvenating
forbs and grasses and reducing
encroachment of native trees and
shrubs. Fire can be both beneficial and
detrimental depending on location, size,
and intensity and is not expected to be
a rangewide threat in the foreseeable
future. Although there has been low to
moderate levels of native tree and shrub
encroachment in nearly all the
populations, most likely as a result of
fire suppression, none of the
encroachment is great enough to cause
a documented threat to the Gunnison
sage-grouse at a rangewide level.
Although various factors discussed in
this section are believed to, or could
potentially be, impacting the
populations, these factors have not
caused significant declines in the
species rangewide. Thus, based on the
best scientific and commercial data
available, we have concluded that
destruction, modification, or
curtailment of its habitat or range does
not threaten or endanger the Gunnison
sage-grouse throughout all or a
significant portion of its range in the
foreseeable future.
rwilkins on PROD1PC63 with RULES_2
Overutilization for Commercial,
Recreational, Scientific, or Educational
Purposes
Hunting
Studies suggest that recreational
hunting of sage-grouse may be
compensatory (i.e., harvest replaces
mortality that would have happened
otherwise due to causes such as
predation; or mortality is compensated
by increased productivity (Crawford
1982)), have no measurable effect on
sage-grouse densities (Braun and Beck
1996), or may be additive (i.e., harvest
adds more deaths per year to the total
otherwise attributable to other causes,
and is not compensated by increased
productivity (Zunino 1987; Connelly et
al. 2000a)). Johnson and Braun (1999)
concluded that harvest mortality may be
additive for sage-grouse if adult females
and young birds sustain the highest
hunting mortality within a population.
No studies have demonstrated that
regulated hunting is a primary cause of
widespread reduced numbers of greater
sage-grouse (Connelly et al. 2004).
Hunting of Gunnison sage-grouse is
regulated by the State wildlife agencies
(GSRSC 2005). Hunting in the Gunnison
Basin appears to have been
compensatory, as it had little if any
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Jkt 208001
impact on the population (CDOW,
unpubl. lit. 2005g). However, sagegrouse hunting was eliminated in the
Gunnison Basin in 2000 due to concerns
with meeting population objectives as
suggested in the Gunnison Basin
Conservation Plan (1997). It is not
known if hunting contributed to the
failure to meet these objectives. Hunting
has not occurred in the other Colorado
populations of Gunnison sage-grouse
since 1995 when the Pinon Mesa area
was closed (GSRSC 2005). Utah has not
allowed hunting since 1989. Both States
have committed to disallow hunting
until the species is no longer a
candidate for listing or no longer
federally-listed and will only consider
hunting if populations can be sustained
(GSRSC 2005). With this finding that
situation will no longer be applicable.
However, the Gunnison Basin Plan calls
for a minimum of 500 birds before
hunting will occur. Although that level
is substantially exceeded in the
Gunnison Basin, we believe the States
sensitivity to the status of the species
would preclude them from opening a
hunting season until at least a majority
of the populations have achieved such
a status. We do not anticipate hunting
to be opened in the foreseeable future in
the smaller populations, or in the near
future in the Gunnison Basin.
Furthermore, any hunting will be
restricted to only 5–10 percent of the
fall population, and will be structured
to limit harvest of females to the extent
possible (GSRSC 2005). Public input
will be considered when determining if
hunting seasons should be reinstated
(GSRSC 2005). We are not aware of any
studies or other data that demonstrate
that poaching (illegal harvest) has
contributed to Gunnison sage-grouse
population declines in either State.
Lek Viewing
The Gunnison sage-grouse is a newly
designated species, which prompts bird
watchers to view it for their ‘‘life lists’’
and may lead to disturbance in
commonly known leks. Daily human
disturbances on sage-grouse leks could
cause a reduction in mating, and some
reduction in total production (Call and
Maser 1985). Boyko et al. (2004, as cited
in GSRSC 2005) determined that 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.
Smaller lek sizes have been
hypothesized to be less attractive to
females, thereby conceivably reducing
the numbers of females mating there.
Disturbance during the peak of mating
also could result in some females not
breeding (GSRSC 2005). Lek viewing
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19973
might affect nesting habitat selection by
females (GSRSC 2005), 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).
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 activities, although
no scientific studies were conducted
(BLM, unpubl. lit. 2005i; GSRSC 2005).
A comparison of male counts on a
designated viewing lek versus male
counts on other leks in the general area,
show that the viewing lek’s counts
followed the same trend line as leks in
the rest of the area (GSRSC 2005). Lek
viewing protocols on designated leks
have generally been followed (GSRSC
2005). Two lek-viewing tours are
organized and led by UDWR per year in
the Monticello group without noticeable
effects (Guy Wallace, UDWR, pers.
comm. 2006). Data collected by CDOW
indicates that controlled lek visitation
also has not impacted greater sagegrouse (GSRSC 2005).
Scientific Research
Gunnison sage-grouse have been the
subject of scientific research studies,
some of which included the capture and
handling of the species. Few, direct
mortalities have occurred during recent
studies and it does not appear that
research is having any significant
impacts on the sage-grouse (Apa 2004;
CDOW, unpubl. lit. 2005g). Most
research is conducted in the Gunnison
and San Miguel Basin populations; the
two largest populations. Based on the
available information, we believe
scientific research on Gunnison sagegrouse is a relatively minor impact, with
only short-term effects to individuals in
localized areas.
Conclusion for Factor B
We have no evidence suggesting that
hunting has resulted in overutilization
of Gunnison sage-grouse. Future
hunting restrictions should adequately
conserve Gunnison sage-grouse. Based
on limited data it appears that lek
viewing has not affected the Gunnison
sage-grouse and lek viewing protocols
designed to reduce disturbance have
generally been followed. Scientific
research appears to be limited to short-
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term impacts of individuals in localized
areas and is not a rangewide 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 threaten
or endanger the sage-grouse throughout
all or a significant portion of its range
in the foreseeable future.
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C. Disease or Predation
Disease
Nothing 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; Schroeder et al.
1999). Some early studies have
suggested that greater sage-grouse
populations are adversely affected by
parasitic infections (Batterson and
Morse 1948). 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
death (Connelly et al. 2004). 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).
Parasites also have been implicated in
greater sage-grouse mate selection, with
potentially subsequent effects on the
genetic diversity of this species (Boyce
1990; Deibert 1995). Connelly et al.
(2004) note that while these
relationships may be important to the
long-term ecology of greater sage-grouse,
they have not been shown to be
significant to the immediate status of
populations. However, Connelly et al.
(2004) have suggested that diseases and
parasites may limit isolated sage-grouse
populations such as most of the
Gunnison sage-grouse populations.
However, we have no evidence
indicating that bacterial or parasitic
diseases are affecting Gunnison sagegrouse individuals or populations.
Greater sage-grouse also are subject to
a variety of bacterial, fungal, and viral
pathogens. The bacteria Salmonella
spp., has caused mortality in the greater
sage-grouse; the bacteria is apparently
contracted through exposure to
contaminated water supplies around
livestock stock tanks (Connelly et al.
2004). Other bacteria found in sagegrouse include Escherichia coli,
botulism (Clostridium spp.), avian
tuberculosis (Mycobacterium avium),
and avian cholera (Pasteurella
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Jkt 208001
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). We have
no reason to expect that mortality and
exposure risk are different in Gunnison
sage-grouse.
West Nile virus (WNv; Flavivirus) was
first diagnosed in greater sage-grouse in
2003, and has been shown to affect their
survival rates. Experimental results,
combined with field data, suggest that a
widespread WNv infection could
negatively affect greater sage-grouse
(Naugle et al. 2004; Naugle et al. 2005).
Summer habitat requirements of sagegrouse potentially increase their
exposure to WNv. Sage-grouse hens and
broods congregate in mesic habitats in
the mid- to late summer, thereby placing
them in the same potential habitats as
the WNv mosquito (Culex spp.), vector
when the mosquitoes are likely to be
active. Surface water sources that have
been created for agricultural, livestock,
and energy and mining activities may
increase the contact between sagegrouse and the mosquito vector. To date,
WNv has not been documented in
Gunnison sage-grouse despite the
presence of WNv-positive mosquitoes in
all counties throughout their range
(Colorado Department of Public Health
2004; U.S. Centers for Disease Control
and Prevention 2004). Although WNv
may be a potential threat, the data
available to date suggest that it is not a
significant threat to Gunnison sagegrouse.
Predation
Predation is the most commonly
identified cause of mortality in sagegrouse (Bergerud 1988; Schroeder et al.
1999; Connelly et al. 2000b). The
composition and density of predator
communities can vary greatly across
space and time (Greenwood 1986;
Johnson et al. 1989; Sargeant et al. 1993;
Sovada et al. 1995). The effect of
predation on the demographic structure
and population fluctuations of
Gunnison sage-grouse is unknown will
depend on the composition of the
predator community, grouse population
levels, and habitat condition. In a study
of nesting Gunnison sage-grouse, Young
(1994) documented only 1 predation
event in 37 nesting attempts. Predation
on greater sage-grouse has been well
documented. Predators of adult greater
sage-grouse include coyotes (Canis
latrans), bobcats (Lynx rufus), weasels
(Mustela spp.), golden eagles, red-tailed
hawks (Buteo jamaicensis), Swainson’s
hawks (B. swainsoni), and ferruginous
hawks (B. regalis) (Hartzler 1974;
Schroeder et al. 1999; Schroeder and
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Baydack 2001). Avian predators,
primarily corvids (Corvus spp.), were
major predators of greater sage-grouse
nests in Idaho (Autenrieth 1981) and
Washington (Vander Haegen 2002),
while ground squirrels and badgers
(Taxidea taxus) were major nest
predators in Wyoming (Patterson 1952).
Most mammalian predation is on eggs;
only coyotes and red foxes (Vulpes
vulpes) are likely to prey on all sagegrouse life stages (GSRSC 2005). Young
(1994) found that the most common
predators of Gunnison sage-grouse eggs
were weasels, ground squirrels, coyotes,
and corvids. Most other raptor predation
of sage-grouse is on juveniles and older
age classes (GSRSC 2005).
Predation rates vary seasonally. The
period of highest mortality for yearling
and adult males occurs during the
lekking season, as they are very
conspicuous while performing their
mating display. Adult female greater
sage-grouse are most susceptible to
predators while on the nest or during
brood-rearing when they are with young
chicks (Schroeder and Baydack 2001).
Autenrieth (1981) concluded that
predation of eggs was the most
important population constraint in
Idaho at that time, and this appears to
be the case for Gunnison sage-grouse,
based on limited data (Young 1994).
Schroeder and Baydack (2001) suggest
that high variation in nest success may
be due to nest predators. Nest predation
may be higher, more variable, and have
a greater impact on small, fragmented
Gunnison sage-grouse populations
(GSRSC 2005).
The population viability analysis of
Gunnison sage-grouse (GSRSC 2005)
found that mortality of chicks and
breeding-age hens contributed
substantially to increasing the relative
probability of extinction because these
two groups contribute most significantly
to population productivity. Gregg et al.
(2003a, 2003b) found that chick
predation mortality in greater sagegrouse ranged from 10 to 51 percent
from 2002–2003 on three study sites in
Oregon. The juvenile mortality rate,
during the first few weeks after
hatching, has been estimated to be 63
percent (Wallestad 1975 in Schroeder
and Baydack 2001). While chicks are
very vulnerable to predation during this
period, other causes of mortality, such
as weather, are included in this
estimate.
Female Gunnison sage-grouse with
nests that were predated nested in sites
with lower shrub density and lower forb
and grass cover (Young 1994). Habitat
alteration that reduces cover for young
greater sage-grouse chicks can increase
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the rate of predation on this age class
(Schroeder and Baydack 2001).
Increasing residential development
increases the likelihood that feral cats
(Felis domesticus) and dogs (Canis
domesticus) will be introduced into
local Gunnison sage-grouse populations.
Development also can contribute to
increased populations of predators (e.g.,
red foxes, American crows (Corvus
americanus)) that are frequently
associated with altered landscapes
(GSRSC 2005). Agricultural
development, landscape fragmentation,
and human populations have the
potential to increase predation pressure
by forcing birds to nest in marginal
habitats, by increasing travel time
through habitats where they are
vulnerable to predation, and by
increasing the diversity and density of
predators (Ritchie et al. 1994; Schroeder
and Baydack 2001; Connelly et al. 2004;
Summers et al. 2004). Where greater
sage-grouse habitat has been altered in
localized areas, the influx of predators
can limit populations (Gregg et al. 1994;
Braun 1998; DeLong et al. 1995;
Schroeder and Baydack 2001). Habitat
fragmentation and the resultant
predation increase may be a limiting
factor for the Gunnison sage-grouse
(Oyler-McCance et al. 2001).
Municipal solid waste landfills have
been shown to contribute to increases in
common raven populations (Knight et
al. 1993; Restani et al. 2001). Ravens are
known to prey on sage-grouse and have
been considered a restraint on sagegrouse population growth in some
locations (Batterson and Morse 1948;
Autenrieth 1981). However, no studies
could be found that linked landfill
presence, common raven populations,
and sage-grouse population levels.
The effect of predation on the
fluctuations and viability of sage-grouse
populations has never been investigated
(Connelly and Braun 1997; Connelly et
al. 2000b; Schroeder and Baydack
2001). Research conducted to determine
survival and nest success in greater
sage-grouse concluded that predation
typically does not limit sage-grouse
numbers (Connelly and Braun 1997;
Connelly et al. 2000a; Connelly et al.
2000b; Wambolt et al. 2002). This
conclusion is supported by evidence
showing that predator removal does not
have long-lasting effects on sage-grouse
population size or stability over large
regions (Cote and Sutherland 1997;
Schroeder et al. 1999; Wambolt et al.
2002). For example, Slater (2003)
demonstrated that coyote control failed
to produce an effect on greater sagegrouse nesting success in southwestern
Wyoming. In their review of literature
regarding predation, Connelly et al.
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(2004) 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. However, both
studies indicated that low nest success
due to predation was ultimately related
to poor nesting habitat. Connelly et al.
(2004) further noted that the idea that
predation is not a widespread factor
depressing sage-grouse populations is
supported by studies of nest success
rates, by the relatively high survival of
adult birds, and by the lack of an effect
on nesting success as a result of coyote
control.
In a study of 28 radio-collared
Gunnison sage-grouse in the Monticello
group, 11 birds died, but only 4 of these
could be attributed to predation by
coyotes or eagles (San Juan County
GSWG, unpubl. lit. 2005). However,
demographic studies of Gunnison sagegrouse in the San Miguel Basin
population suggests, but does not
conclusively prove, that predation may
be affecting this population (CDOW,
unpubl. lit. 2005g). No information is
available for the other populations
considered.
Conclusion for Factor C
No rangewide or population level
impacts of bacterial, viral, fungal, or
parasitic diseases on Gunnison sagegrouse have been reported, including
WNv. Predation is occurring at some
level in all populations, but we have no
evidence to suggest that it is a
population or rangewide threat to
Gunnison sage-grouse. Thus, based on
the best scientific and commercial data
available, we have concluded that
disease and predation do not threaten or
endanger the sage-grouse throughout all
or a significant portion of its range in
the foreseeable future.
D. The Inadequacy of Existing
Regulatory Mechanisms
Local Laws and Regulations
Approximately 43 percent of
occupied Gunnison sage-grouse habitat
is privately owned (GSRSC 2005).
Gunnison County and San Miguel
County, Colorado, are the only entities
that have ordinances within the species’
range that provide a level of
conservation consideration specifically
for the Gunnison sage-grouse or their
habitats on private land (Dolores County
2002; Mesa County, unpubl. lit. 2003;
Montrose County 2003). In 2001,
Gunnison County, Colorado developed
Land Use Resolutions (LUR) to be
consistent with the Memorandum of
Agreement (MOA) signed for the
Gunnison Basin Conservation Plan in
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1998 (Gunnison County 2001). In the
MOA, Gunnison County agreed to
‘‘* * * reasonably consider sage-grouse
conservation actions in its regulation of
land use * * *’’ and to implement the
Gunnison Basin Conservation Plan to
the best of their ability. The County is
attempting to utilize this LUR to
optimize sage-grouse conservation. In
2003, the LUR was revised slightly to
allow two houses on 35 acres rather
than one house without County review,
thereby increasing the housing density
that could occur in sage-grouse habitat.
In 2005, San Miguel County amended
its Land Use Codes to include
consideration and implementation, to
the extent possible, of conservation
measures for the sage-grouse when
considering land use activities and
development located in Gunnison sagegrouse habitat (San Miguel County,
unpubl. lit. 2005). In addition to the
county protections, Gunnison County
has hired a Gunnison Sage-grouse
Coordinator and organized a Strategic
Committee to facilitate implementation
of conservation measures in the
Gunnison Basin under both the local
Conservation Plan and RCP. San Miguel
County has recently hired a Gunnison
Sage-grouse Coordinator for the San
Miguel Basin population. The efforts of
these two counties reflect positively on
their willingness to conserve Gunnison
sage-grouse.
Colorado State statute (C.R.S. 30–28–
101) exempts parcels of land of 14 ha
(35 ac) or more per home from
regulation, so county zoning laws in
Colorado can only restrict developments
with housing densities greater than one
house per 14 ha (35 ac). This situation
allows some parcels to be exempt from
county regulation and may negatively
affect some sage-grouse. However, we
have no data to indicate that this is
threatening individual populations or
individuals. We could find no data on
the precise threshold of the number of
acres per house that will affect
Gunnison sage-grouse.
Habitat loss is not regulated or
monitored in Colorado counties where
Gunnison sage-grouse occurs. 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.
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
were unable to obtain information
regarding the nature or extent of zoning
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efforts and their direct or indirect effects
on populations and habitats.
State Laws and Regulations
Colorado Revised Statutes, Title 33
Article 1 give 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. 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 sage-grouse.
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. However, in 2000, CDOW
closed the hunting season for Gunnison
sage-grouse 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 and a sensitive
species in Utah providing heightened
priority for management (Gary Skiba,
CDOW, pers. comm. 2006; Guy Wallace,
UDWR pers. comm. 2006).
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 3).
Some of the easements include
conservation measures that are specific
for Gunnison sage-grouse, while most
are directed at other species, such as big
game (GSRSC 2005). We are aware that
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some of these easements do protect
existing sage-grouse habitat. However,
we do not have information on the
location or size of the easements with
sage-grouse specific conservation
measures and, therefore, cannot assess
their overall value to Gunnison sagegrouse.
considered negligible. The UDWR does
not own any land within occupied
habitat in Utah. The CDOW owns 2
percent of the occupied habitat in
Colorado, with some management for
Gunnison sage-grouse on those lands.
Federal Laws and Regulations
Gunnison sage-grouse are not covered
TABLE 3.—ACRES OF CONSERVATION or managed under the provisions of the
EASEMENTS BY POPULATION AND Migratory Bird Treaty Act (16 U.S.C.
PERCENTAGES OF OCCUPIED HABI- 703–712). Federal agencies are
responsible for managing 55 percent of
TAT PROTECTED BY EASEMENTS the total Gunnison sage-grouse habitat
(GSRSC 2005)
(GSRSC 2005). The Federal agencies
with the most sagebrush habitat are
Occupied
BLM, an agency of the Department of
Number of
Population
habitat
acres
the Interior, and USFS, an agency of the
(percent)
U.S. Department of Agriculture. The
Gunnison Basin
26,145
4 NPS in the Department of the Interior
San Miguel
also has responsibility for lands that
Basin .............
844
1 contain sage-grouse habitat.
Monticello ..........
2,560
1
About 42 percent of occupied habitat
˜
Pinon Mesa .......
7,314
19 is on BLM-administered land (GSRSC
Crawford ...........
523
2 2005). The Federal Land Policy and
Management Act of 1976 (FLPMA) (43
The CDOW has been gathering
U.S.C. 1701 et seq.) is the primary
information from landowners who may
Federal law governing most land uses
be interested in signing up under the
on BLM-administered lands. Section
CCAA referenced earlier in this
102(a)(8) of FLPMA specifically
document. As of January 2006, 72
recognizes wildlife and fish resources as
landowners owning 41,278 ha (102,000
being among the uses for which these
ac) have expressed an interest in
lands are to be managed. Regulations
enrolling their lands under the CCAA.
pursuant to FLPMA and the Mineral
States regulate non-coal mining in the Leasing Act (30 U.S.C. 181 et seq.) that
United States. Colorado law (State
address wildlife habitat protection on
Statute Title 34, Article 32) contains
BLM-administered land include 43 CFR
language intended to protect wildlife
3162.3–1 and 43 CFR 3162.5–1; 43 CFR
resources through appropriate
4120 et seq.; 43 CFR 4180 et seq.
reclamation and encourages
Resource Management Plans (RMPs)
revegetation using native species. Utah
are the basis for all actions and
mining regulations (R647–4–110) allow
authorizations involving BLMreclamation to wildlife resource use.
administered lands and resources. They
We are not aware of any conservation establish allowable resource uses;
measures implemented for potential oil
resource condition goals and objectives
and gas development impacts to
to be attained; program constraints and
Gunnison sage-grouse on private lands
general management practices needed to
underlain with privately-owned
attain the goals and objectives; general
minerals, which are regulated by the
implementation sequences; and
Colorado Oil and Gas Conservation
intervals and standards for monitoring
Commission or the Utah Division of Oil, and evaluating the plan to determine its
Gas, and Mining. Colorado and Utah
effectiveness and the need for
have laws that directly address the
amendment or revision (43 CFR 1601.0–
priorities for use of State school section
5(k)).
lands, which require that management
The RMPs provide a framework and
of these properties be based on
programmatic guidance for activity
maximizing financial returns. We are
plans, which are site-specific plans
not aware of any conservation measures written to implement decisions made in
established for Gunnison sage-grouse on a RMP. Examples include Allotment
State school section lands other than a
Management Plans that address
request to withdraw or apply ‘‘no
livestock grazing, oil and gas field
surface occupancy’’ and conservation
development, travel management, and
measures from the RCP to four sections
wildlife habitat management. Activity
available for oil and gas leasing in the
plan decisions normally require
San Miguel Basin population (see Factor additional planning and National
A for further discussion). State school
Environmental Policy Act (NEPA)
section lands account for only 1 percent analysis. Within the Gunnison Basin
of occupied habitat in Colorado and 1
population 56 percent of the BLM
percent in Utah so impacts may be
allotment acreage in occupied habitat
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currently has Gunnison sage-grouse
habitat objectives incorporated into the
allotment management plans (BLM,
unpubl. lit. 2005h). Rangewide, only 20
percent of BLM grazing allotments have
thus far incorporated Gunnison sagegrouse conservation measures and/or
habitat objectives into the allotment
management plans or in permit
renewals.
On November 16, 2004, BLM
Instruction Memorandum (IM) 2005–
024 transmitted information to all BLM
field and Washington Office officials
regarding the development of a National
BLM Sage-grouse Habitat Conservation
Strategy for BLM-administered lands.
This strategy is described as the
framework to address the conservation
of sage-grouse and risk to sagebrush
habitats on lands and activities
administered by BLM. It commits BLM
to work with States and local interests
on this issue. The IM instructed BLM
State Directors to develop a process and
schedule to update deficient RMPs to
adequately address sage-grouse and
sagebrush conservation needs. The BLM
has developed a process to update RMPs
in Colorado, and has notified the
Service of general timeframes for RMP
updates but specific deadlines have not
been provided. The BLM continues to
update applicable RMPs and activity
plans.
The BLM has regulatory authority for
oil and gas leasing, as provided at 43
CFR 3100 et seq., and they are
authorized to require stipulations as a
condition of issuing a lease. The BLM’s
planning handbook has programspecific 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). 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). The BLM has
regulatory authority to condition
‘‘Application for Permit to Drill’’
authorizations, conducted under a lease
that does not contain sage-grouse
conservation stipulations (BLM 2004).
Also, oil and gas leases have a 200 m
(650 ft) stipulation, which allows
movement of the drilling area by that
distance (BLM 2004). The BLM states
that many of their field offices work
with the operators to move a proposed
drilling site farther or justify such a
move through the site-specific NEPA
process (BLM 2004).
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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 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 acreages in the Crawford Area
and Gunnison Basin populations are
covered by this policy. However, leases
˜
already exist in 17 percent in the Pinon
Mesa population, and 49 percent in the
San Miguel Basin population.
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–
4). The Service has no information
indicating that the BLM has granted a
significant number of waivers of
stipulations pertaining to the Gunnison
sage-grouse and/or 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, section 6217(a)). On May 18, 2001,
the President signed Executive Order
13212—Actions to Expedite EnergyRelated Projects (66 FR 28357, May 22,
2001), which states that it is the
Administration’s policy 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. The BLM
has responded to these declarations
with the issuance of several IMs to their
staff that may influence sage-grouse
conservation during these actions,
including providing guidance for
planning relative to oil and gas
operations and focusing efforts for
resource recovery in seven areas, two of
which are within Gunnison sage-grouse
habitats (IM 2003–137, April 3, 2003; IM
2003–233, July 28, 2003; IM CO–2005–
038, July 12, 2005).
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The BLM regulatory authority for
grazing management is provided at 43
CFR part 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
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 part 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. Since
Gunnison sage-grouse habitats are a
special status species, these standards
will specifically address the habitat
requirements of the Gunnison Sage
Grouse and help to minimize any
threats and improve existing habitats.
On December 8, 2003, BLM issued a
proposed rule (68 FR 68452) to modify
the current grazing management
regulation in two ways: (1) It provides
that assessment and monitoring
standards are needed to support a
determination that livestock grazing
significantly contributes to not meeting
a standard or conforming with a
guideline; and (2) it requires BLM to
analyze, formulate and propose
appropriate action within 24 months of
the determination rather than before the
start of the next grazing year.
In signing the RCP (GSRSC 2005),
BLM has agreed to follow
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recommendations for conservation
efforts addressing the effects of grazing,
oil and gas development and other
threats, within the constraints of
existing laws, policies, regulations, and
management plans, and while
considering the needs or implications to
other species and multiple uses. It will
take time for BLM to address the time
requirement necessary to revise and
formally incorporate Gunnison sagegrouse conservation measures and
habitat objectives in all of their RMPs
through a rulemaking. In the meantime,
the Colorado Office of the BLM issued
IM CO–2005–038, which provides an
interim policy to implement the RCP.
The IM directs that the RCP guidance
and strategies be applied through sitespecific analysis consistent with NEPA
for all projects or actions in Gunnison
sage-grouse habitat. For surface
disturbing activities such as oil and gas
development the IM directs BLM staff to
work with the operator to minimize
habitat loss and fragmentation.
Moreover, if the local conservation
plans for each population have
additional measures that address local
conditions the IM directs BLM staff to
consider if they are more effective than
guidance in the RCP and, if so, to
implement them. Full implementation
of the RCP, according to the IM, will
occur as guidance and strategies are
considered and analyzed during RMP
revisions and/or amendments. These
actions will contribute to the
conservation of the Gunnison Sage
Grouse and help to minimize any
potential threat from activities on
Federal lands in the Gunnison’s range.
The USFS has management authority
for 10 percent of the occupied Gunnison
sage-grouse habitat (GSRSC 2005).
Management of Federal activities on
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).
This has historically been done through
a NEPA process, including 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 1982 NFMA implementing
regulation for land and resource
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management planning (1982 rule, 36
CFR part 219), under which all existing
forest plans were prepared, requires
USFS to manage habitat to maintain
viable populations of existing native
vertebrate species on National Forest
System lands (1982 rule, 36 CFR
219.19). A new USFS planning
regulation was promulgated on January
5, 2005 (70 FR 1023). Under the new
regulation a desired condition
description and guidelines will be
provided, rather than a set of
prescriptive standards that apply to
projects. Planning, and decisions for
projects and activities, will address sitespecific conditions and identify
appropriate conservation measures to
take for each project or activity.
Under the new regulation, the
purpose of forest plans is to establish
goals and to set forth guidance to follow
in pursuit of those goals. The rule calls
for five components of plans: Desired
conditions; objectives; guidelines;
suitability of areas; and special areas (36
CFR 219.7(a)(2)). The rule states that
these components are intended to
provide general guidance and goals or
other information to be considered in
subsequent project and activity
decisions, and that none of these
components are commitments or final
decisions approving projects and
activities (36 CFR 219.7(a)(2)). Approval
of a plan, plan amendment, or plan
revision comprised of these five
components may be categorically
excluded from NEPA documentation (36
CFR 219.4(b)).
The new regulation requires plans to
provide a framework to contribute to
sustaining native ecological systems by
providing ecological conditions to
support diversity of native plants and
animal species in the plan area (36 CFR
219.10 (b)). Ecosystem diversity is
described as being the primary means
by which a plan contributes to
sustaining ecological systems (36 CFR
219.10 (b)), and USFS states that this
focus is expected to conserve most
species. The regulation defines speciesof-concern as ‘‘Species for which the
Responsible Official determines that
management actions may be necessary
to prevent listing under the Endangered
Species Act’’ (36 CFR 219.16).
For each unit of the National Forest
System, the transition period for the
new regulation is 3 years (36 CFR
219.14). A document approving a plan
developed, revised, or amended using
the new regulation must include a
description of the effects of the plan on
existing permits, contracts, or other
instruments implementing approved
projects and activities (36 CFR 219.8(a)).
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The Gunnison sage-grouse is
designated as a USFS sensitive species
in Region 2 (Colorado) and Region 4
(Utah), thereby ensuring and enhancing
the management awareness of the
species under the new planning rule.
The forests within the range of sagegrouse provide important seasonal
habitats for the species, particularly the
Grand Mesa, Uncompahgre, and
Gunnison National Forests. While the
1982 planning regulation, including its
provision for population viability, was
used in the development of the existing
Forest Plans, no information has been
provided regarding specific
implementation of the above new
regulations and policies for the
Gunnison sage-grouse. However, any
agency action taken under the new
planning rule will require consideration
of Gunnison Sage Grouse habitat.
We did not receive information from
the USFS on whether habitat objectives
and conservation measures have yet
been incorporated into grazing
allotments and whether local
conservation plan sage-grouse habitat
objectives and conservation measures
have been incorporated into Forest
Plans or LRMPs.
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. However, the
only population with USFS lands that
are 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).
The NPS is responsible for managing
2 percent of occupied Gunnison sagegrouse habitat (GSRSC 2005). 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 wildlife
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 Recreation Area
include portions of occupied habitat of
the Crawford and Gunnison Basin
populations. Gunnison sage-grouse
conservation measures are not included
in the General Management Plan, but
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are included in current RMPs. They also
will be incorporated when the RMPs are
revised or amended. The NPS is
currently following conservation
measures in the local conservation plans
and the RCP (Myron Chase, NPS, pers.
comm. 2005).
The NRCS of the U.S. Department of
Agriculture assists farmers, ranchers,
and other private landowners in
reducing threats to sage-grouse habitat
by providing technical assistance and
financial resources to support
management and habitat restoration
efforts, helping farmers and ranchers
maintain and improve habitat as part of
larger management efforts, and
developing technical information to
assist NRCS field staff with sage-grouse
considerations when working with
private landowners. The NRCS has the
Wildlife Habitat Incentive Program and
Environmental Quality Incentive
Program that can be used to fund
projects implementing conservation
measures in Gunnison sage-grouse
habitat. The Service’s Partners for Fish
and Wildlife Program also can fund
conservation measures for Gunnison
sage-grouse. All of these programs have
contributed to Gunnison Sage Grouse
conservation within its range by
converting croplands to habitat
improving habitat or restoring habitat.
Conclusion for Factor D
Gunnison sage-grouse conservation
has been addressed through numerous
local, State, and Federal plans, laws,
regulations, and policies. Current
county regulations provide some ability
to limit impacts to sage-grouse habitat
from housing developments where the
area is zoned for under 14 ha (35 ac) per
house. Both counties where the largest
populations of Gunnison sage-grouse
occur have Land Use Resolutions or
Codes to promote Gunnison sage-grouse
conservation. The CDOW and UDWR
have implemented and continue to
pursue conservation easements in
Colorado and Utah, respectively, to
conserve Gunnison sage-grouse habitat
and the species’ needs. State wildlife
regulations provide opportunities to
address other conservation needs of the
species.
Impacts resulting from current leases
for oil and gas development on Federal
lands are regulated at the ‘‘Application
for Permit to Drill’’ stage as protective
stipulations are applied through
guidance in IM CO–2005–038. Grazing
impacts are regulated with existing
laws, regulations, and policies. Laws,
regulations, and policies guiding
development and implementation of
land management plans for all the
Federal agencies, address conservation
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of Gunnison sage-grouse habitat. In light
of the fact that implementation of the
aforementioned laws, regulations, and
policies has not resulted in a decline
within recent timeframes, as analyzed
by Garton (2005) and, based on the best
scientific and commercial data available
we have concluded that inadequacy of
existing regulatory mechanisms does
not threaten or endanger the sage-grouse
throughout all or a significant portion of
its range in the foreseeable 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, and pesticides.
Genetics
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
(Charlesworth and Charlesworth 1987)
or by reducing the overall fitness of
individuals in the population. Estimates
for how large populations must be to
prevent inbreeding depression vary
dramatically. For example, Lande
(1995b), Lynch et al. (1995), and
Charlesworth et al. (1993) suggested that
populations will need to have a genetic
effective population size of 1,000, 100,
and 12 individuals, respectively, to
avoid accumulating deleterious
mutations. However, if mutation
accumulation is a threat to small
populations, it is expected to take
hundreds to thousands of generations to
occur (GSRSC 2005).
Oyler-McCance et al. (2005)
investigated population structure of
Gunnison sage-grouse using
mitochondrial DNA sequence data from
seven geographic areas (Cerro SummitCimarron-Sims Mesa, Crawford,
Gunnison Basin, Curecanti area of the
Gunnison Basin, Monticello-Dove
˜
Creek, Pinon Mesa, and San Miguel
Basin). They found that levels of genetic
diversity were highest in the Gunnison
Basin, which consistently had more
alleles and contained most of the alleles
present in other populations. All other
populations had much lower levels of
diversity. These 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
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of the species, but collectively it is
possible that 24 percent of the genetic
diversity is important to future
rangewide survival of the species. All
populations sampled were found to be
genetically discrete units (OylerMcCance et al. 2005), 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 drought), 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).
Historically, the Monticello-Dove
˜
Creek, San Miguel, Crawford, and Pinon
Mesa populations were larger and were
connected through more contiguous
areas of sagebrush habitat. OylerMcCance et al. (2001) documented a 20
percent loss and 37 percent
fragmentation of sagebrush habitat in
southwestern Colorado between the late
1950s and the early 1990s, 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). However, OylerMcCance et al. (2005) 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 itself appeared to have a
mixture of individuals with differing
probabilities of belonging to different
clusters. This suggests that the San
Miguel population may act as a conduit
of gene flow among the satellite
populations surrounding the larger
population in Gunnison. Additionally,
Oyler-McCance et al. (2005) found that
another potential disperser into
Crawford was from the Gunnison Basin.
This is not surprising given their close
geographic proximity.
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), suggestions
range from 500–5,000 individuals
(Franklin 1980; Lande and
Barrowclough 1987; Lande 1995a).
Similarly, population sizes in the upper
100s–1,000s are reported to be required
for a higher probability of persistence
over 100 years (Shaffer 1987). While the
persistence of wild populations is
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usually influenced more by ecological
rather than by genetic effects, once they
are reduced in size, genetic factors
become increasingly important (Lande
1995a).
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Population Viability Analysis
The CDOW contracted for a
population viability analysis (PVA) for
the Gunnison sage-grouse (Miller 2004).
The PVA is a tool used to predict the
probability of extinction for a wildlife
population under various management
scenarios. They are typically based on
available population data which are
often inadequate for a complete
understanding of complex systems.
Therefore, PVAs only provide an
approximation of how a species may
respond to various management
alternatives without consideration of
threats, since data are not available to
determine how demographic rates will
be affected by factors such as habitat
loss or fragmentation. Also, since a PVA
is a model, it does not present a
complete picture of the system (GSRSC
2005 and references therein).
The purpose of the Gunnison sagegrouse PVA was to assist the CDOW in
evaluating the relative risk of extinction
for each population under the current
conditions (i.e. the risk of extinction if
nothing changes) and 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).
The results of this 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 suggest that the Gunnison Basin
population is likely to persist long term
and, 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 may be extirpated
(GSRSC 2005). Loss of genetic diversity
from the extirpation of the two
populations and the group would not
result in a substantial effect to the
species as a whole, because their genetic
composition is largely represented in
the other populations. The remaining
populations currently have estimated
numbers between 150 and 350 birds, up
from 125–250 in 2004, and their relative
extinction risk as determined by the
PVA is between those extremes.
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Garton’s (2005) analysis of population
trends also supports a relatively stable
rangewide population, as well as a
stable Gunnison Basin population for
the last 10 years and longer. The RCP
(GSRSC 2005) identified the need to
increase gene flow among populations
by improving corridors for betweenpopulation movement or translocation
of selected genotypes from the
Gunnison Basin to smaller populations,
and vice-versa for population
augmentation and maintenance of
genetic diversity.
Oyler-McCance et al. (2005)
conducted a genetic analysis of
Gunnison sage-grouse populations using
mitochondrial DNA sequence and
nuclear microsatellite data. The Cerro
Summit-Cimarron-Sims Mesa
population was not included in this
analysis due to inadequate sample sizes.
The Poncha Pass population also was
not included as it is composed of
individuals transplanted from Gunnison
Basin. In general, Gunnison sage-grouse
have low levels of genetic diversity
when compared to the greater sagegrouse (Oyler-McCance et al. 2005).
Within the species, the Gunnison Basin
birds had higher levels of genetic
diversity than the other populations.
Lower genetic diversity is consistent
with small population size and
geographical isolation (Oyler-McCance
et al. 2005).
In summary, although the Cerro
Summit-Cimarron-Sims Mesa and
Poncha Pass populations and the Dove
Creek group of the Monticello-Dove
Creek population may become
extirpated in the near future, their
genetic characteristics are largely
represented in the remaining
populations.
Drought/Weather
Drought is a common occurrence
throughout the range of the Gunnison
sage-grouse (Braun 1998). Drought
reduces vegetation cover (Milton et al.
1994; Connelly et al. 2004), 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. Approximately 2,544 sq km
(982 sq mi) of sagebrush shrublands
died in Utah in 2003 as a result of
drought and infestations with the Aroga
(webworm) moth (Connelly et al. 2004).
Sage-grouse are affected by drought
through the potential loss of vegetative
habitat components and reduced insect
production (Connelly and Braun 1997).
These habitat component losses can
result in declining sage-grouse
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populations due to increased nest
predation and early brood mortality
associated with decreased nest cover
and food availability (Braun 1998;
Schroeder et al. 1999).
Greater sage-grouse populations
declined during the 1930s period of
drought (Patterson 1952; Willis et al.
1993; Braun 1998). 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).
Although drought has been a consistent
and natural part of the sagebrush-steppe
ecosystem, drought impacts on sagegrouse can be exacerbated when
combined with other habitat impacts
that reduce cover and food (Braun
1998).
Drought began in the Gunnison Basin
at least by 2001 and was most severe in
2002 (BLM, unpubl. lit. 2005i). The
drought fully or partially killed
approximately 40,470 ha (100,000 ac)
(17 percent) of sagebrush in occupied
range of the sage-grouse in the Gunnison
Basin in 2002 (BLM, unpubl. lit. 2005i).
About 35,000 ha (86,000 ac) had
significant dieback and 5,700 ha (14,000
ac) had moderate to light dieback of
sagebrush and other shrubs. An
estimated 4,000 ha (10,000 ac) (2
percent) had substantial mortality of
grasses and forbs. Phlox spp., a forb that
is important sage-grouse forage in the
spring and summer, had 50- to 80percent mortality in areas where
sagebrush dieback was over 50 percent
(BLM, unpubl. lit. 2005i). In 2003, 48
percent of all sagebrush plants were
defoliated and 17 percent were dead
(Wenger et al. 2003). By 2004, there was
only modest recovery with increased
moisture (BLM, unpubl. lit. 2005i). By
2005, sagebrush plants that were
partially killed were recuperating
(Sandy Borthwick, BLM, pers. comm.
2005).
The drought also affected sagebrush
communities in the San Miguel Basin
population, particularly in the Dry
Creek Basin area. During the late fall
and winter of 2003–2004, CDOW
conducted sagebrush transects in Dry
Creek Basin to monitor drought-related
impacts. Approximately 75 percent of
the sagebrush canopy in Dry Creek
Basin was lost to sagebrush defoliation
due to drought (Wenger et al. 2003).
Although most plants survived and
exhibited signs of recovery in 2003,
large areas, particularly at low elevation,
lost over 90 percent of the plants
(Wenger et al. 2003). These
communities started to recover in the
spring of 2004, and plants that survived
had heavy seed crops in the fall of 2004.
Recuperation of these communities
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continued in 2005 (Kathy Nickell, BLM,
pers. comm. 2005). Detrimental effects
on Gunnison sage-grouse, particularly
on the birds attending the Desert Lek in
Dry Creek Basin were observed after the
drought. This lek had the greatest
number of males counted (12–18) of the
3 leks in the population from 1996
through 2002, but was reduced to 0 in
2004 and 2005 (CDOW, unpubl. lit.
2005b).
In the Monticello group, most nesting
areas are in poor condition due to lack
of herbaceous cover as a result of
drought and grazing (GSRSC 2005).
Long-term drought also has reduced the
availability of wet meadow habitat for
brood-rearing (GSRSC 2005). Rains in
2005 have replenished some wet
meadow habitats or riparian areas
(Tammy Wallace, BLM, pers. comm.
˜
2005). In the Pinon Mesa population the
recent drought may have caused some
limited, but unquantified, sagebrush
and herbaceous understory die-back at
lower elevations. Most plants affected
do not appear to have died completely
and sagebrush conditions have
improved in 2004 and 2005 (CDOW,
unpubl. lit. 2005g). Drought has been
identified as a primary threat to the
Crawford population (Crawford Area
Conservation Plan 1998, GSRSC 2005).
Drought conditions occurred there
between 1999 and 2003 (Jim Ferguson,
BLM, pers. comm. 2005). No
quantitative habitat data are available,
but little grass, forb or sagebrush growth
occurred during this period (Jim
Ferguson, BLM, pers. comm. 2005).
Since 1999, lek counts have declined.
The BLM cut back on grazing animal
unit months and there were no other
identifiable negative impacts to BLM
lands in the area during this timeframe,
suggesting drought as the primary cause
of decline (Jim Ferguson, BLM, pers.
comm. 2005).
The Gunnison sage-grouse is capable
of enduring moderate or severe, but
relatively short-term, drought as
observed from persistence of the
populations during drought conditions
from 1999–2003 throughout much of the
range. Habitat appeared to be negatively
affected by drought across a broad area
of the Gunnison sage-grouse’s range.
However, the reduction of sagebrush
density in some areas, allowing for
greater herbaceous growth, and
stimulating the onset of sagebrush seed
crops (Wenger et al. 2003) may actually
be beneficial to sagebrush habitats over
the long term. As a result, we find that
Gunnison Sage Grouse is not
sufficiently threatened by drought.
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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). Sage-grouse
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).
Recreation from off-highway vehicles,
hikers, mountain bikes, campers,
snowmobiles, bird watching, and other
sources has affected many parts of the
range, especially portions of the
˜
Gunnison Basin and Pinon Mesa
population (BLM, unpubl. lit. 2005i;
CDOW, unpubl. lit. 2005g). 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 land
use on lands managed by BLM
(Connelly et al. 2004) and recreational
use of national forests has increased 76
percent since 1977 (Rosenberg et al.
2004).
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, unpubl.
lit. 2005i). A comprehensive plan to
manage motorized and non-motorized
recreation is not available for BLM land
in the Gunnison Basin, nor has there
been monitoring or research on the
extent of impacts (BLM, unpubl. lit.
2005i). The BLM has seasonal closures
on 17 roads with 6 of these closures
protecting leks, but many more roads
provide access to leks (BLM, unpubl. lit.
2005i). In addition, the Gunnison Field
Office of BLM and Gunnison County
collectively closed numerous roads to
protect leks and nesting habitat within
the Gunnison Basin for April and part
of May 2006. While road closures may
be violated, we have no data indicating
that these violations are affecting the
Gunnison Sage Grouse.
Dispersed camping occurs at a low
level on public lands in all of the
populations, particularly during the
hunting seasons for other species. A
designated campground is located on
BLM land near occupied habitat on
˜
Pinon Mesa (BLM, unpubl. lit. 2005a).
No studies on recreational effects in the
˜
Pinon Mesa population have occurred.
With its proximity to Grand Junction
and expected growth in Mesa County
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19981
and the Glade Park area, recreational
impacts are expected to increase in the
˜
Pinon Mesa population area. However,
we have no data indicating that these
camping activities are adversely
affecting Gunnison Sage Grouse.
Domestic dogs accompanying
recreationists 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 behavior is
affecting Gunnison Sage Grouse.
Pesticides
Insects are an important component of
sage-grouse chick and juvenile diets
(Patterson 1952, Klebenow and Gray
1968, Johnson and Boyce 1990, Fischer
et al. 1996a). Insects, especially ants
(Hymenoptera) and beetles (Coleoptera),
can comprise a major proportion of the
diet of juvenile sage-grouse (Patterson
1952) and are important components of
early brood-rearing habitats (Drut et al.
1994a). 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. Infestations of Russian
wheat aphids (Diuraphis noxia) have
occurred in Gunnison sage-grouse
occupied range in Colorado and Utah
(GSRSC 2005). Disulfoton, a systemic
organophosphate extremely toxic to
wildlife, was routinely applied to over
a million acres of winter wheat 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). One instance of
greater sage-grouse mortality was
reported following application of
organophosphate and carbamate
pesticides to cultivated crops in Idaho
(Blus et al. 1989). More recently, an
infestation of army cutworms (Euxoa
auxiliaries) occurred in sage-grouse
habitat along the Utah-Colorado State
line. Thousands of acres of winter wheat
and alfalfa fields were sprayed with
insecticides such as permethrin by
private landowners to control them
(GSRSC 2005) but again, we have no
data indicating any, adverse effects to
Gunnison sage grouse.
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impact of pesticides on Gunnison sagegrouse 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 do not
threaten or endanger the sage-grouse
throughout all or a significant portion of
its range in the foreseeable future.
Conclusion for Factor E
Although genetic consequences of low
Gunnison sage-grouse population
numbers could express themselves,
there is no evidence that genetic factors
have thus far caused a threat to the
Gunnison sage-grouse and it is unlikely
that genetic factors (even without
connectivity corridors or population
augmentation) will be a threat for the
foreseeable future. Effects of the severe
drought centered on the year 2002
appear to have been ameliorated starting
in 2004, and the sage-grouse survived
the drought as they have survived other
droughts in the past. Despite potentially
greater effects to the smaller populations
we have no evidence that drought is a
threat to the survival of the Gunnison
sage-grouse. Although disturbance and
habitat destruction, fragmentation, or
degradation may result from
recreational activities, we have no data
indicating that recreational impacts to
Gunnison sage-grouse to demonstrate
that recreation is or may become a threat
to the species. Based on the available
information, there appears to be
infrequent use of insecticides in
populations of the Gunnison sagegrouse and no data indicating there are
direct adverse effects. The most likely
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Use of insecticides to control
mosquitoes is infrequent and probably
do not have detrimental effects on sagegrouse. Available insecticides that kill
adult mosquitoes include synthetic
pyrethroids such as permethrin, which
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).
Listing Determination
We have assessed the best scientific
and commercial information available
and have determined that the Gunnison
sage-grouse is not warranted for listing
under the Endangered Species Act, as
amended. We also no longer consider
the species to be a candidate for listing.
The 2004 Candidate Notice of Review
retained the listing priority number at a
2 based on perceived imminent threats
of high magnitude. However, based on
information obtained since our 2004
review (e.g., Garton 2005), we have
determined that threats to the Gunnison
sage-grouse are neither imminent or of
such magnitude that they threaten or
endanger the existence of the species.
The PVA (GSRSC 2005) concluded
that the Cerro Summit-Cimarron-Sims
Mesa and Poncha Pass populations and
the Dove Creek group of the MonticelloDove Creek population have a high
probability of extirpation in the
foreseeable future. However, these
populations do not comprise a
significant portion of the Gunnison
sage-grouse range, as they are small and
isolated. Even though these populations
have higher probabilities of extirpation,
we continue to strongly encourage
CDOW and other interested parties to
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take necessary management actions to
prevent their extirpation. For the
remaining populations, numerous
impacts pose potential threats to the
Gunnison sage-grouse when considered
under the listing factors. However, there
is no evidence that the impacts are
causing rangewide threats such that
they are likely to cause the Gunnison
sage-grouse to be in danger of extinction
throughout all or a significant portion of
its range in the foreseeable future.
If impacts to the species rise to the
level of being a threat in the future or
if the Service finds that the populations
are declining significantly faster than
they were found to have done in the
past (Garton 2005), the Service will
reexamine the listing status of the
Gunnison sage-grouse. We will continue
to monitor the status of the Gunnison
sage-grouse and its habitat and will
continue to accept additional
information and comments from all
governmental agencies, the scientific
community, industry, or any other
interested party concerning this finding.
References
A complete list of references used in
the preparation of this finding is
available upon request from the Western
Colorado Field Office (see ADDRESSES
section).
Authority
The authority for this action is the
Endangered Species Act of 1973, as
amended (16 U.S.C. 1531 et seq.).
Dated: April 11, 2006.
H. Dale Hall,
Director, U.S. Fish and Wildlife Service.
[FR Doc. 06–3619 Filed 4–17–06; 8:45 am]
BILLING CODE 4310–55–P
E:\FR\FM\18APR2.SGM
18APR2
Agencies
[Federal Register Volume 71, Number 74 (Tuesday, April 18, 2006)]
[Rules and Regulations]
[Pages 19954-19982]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 06-3619]
[[Page 19953]]
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Part III
Department of the Interior
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Fish and Wildlife Service
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50 CFR Part 17
Endangered and Threatened Wildlife and Plants; Final Listing
Determination for the Gunnison Sage-Grouse as Threatened or Endangered;
Final Rule
Federal Register / Vol. 71, No. 74 / Tuesday, April 18, 2006 / Rules
and Regulations
[[Page 19954]]
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DEPARTMENT OF THE INTERIOR
Fish and Wildlife Service
50 CFR Part 17
Endangered and Threatened Wildlife and Plants; Final Listing
Determination for the Gunnison Sage-Grouse as Threatened or Endangered
AGENCY: Fish and Wildlife Service, Interior.
ACTION: Final listing determination.
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SUMMARY: We, the U.S. Fish and Wildlife Service (Service), announce a
final listing determination for 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 listing is not
warranted. Thus, we no longer consider the species to be a candidate
for listing. We ask the public to submit to us any new information that
becomes available concerning the status of or threats to the species.
This information will help us monitor and encourage the conservation of
this species.
DATES: The determination announced in this document was made on April
11, 2006. Although further listing action will not result from this
determination, we request that you submit new information concerning
the status of or threats to this species whenever it becomes available.
ADDRESSES: Comments and materials received, as well as supporting
documentation used in the preparation of this final listing
determination, will be available for inspection, by appointment, during
normal business hours at the Western Colorado Ecological Services Field
Office, U.S. Fish and Wildlife Service, 764 Horizon Drive, Building B,
Grand Junction, Colorado 81506-3946. Submit new information, materials,
comments, or questions concerning this species to the Service at the
above address.
FOR FURTHER INFORMATION CONTACT: Allan Pfister, Western Colorado
Supervisor (see ADDRESSES section), by telephone at (970) 243-2778, by
facsimile at (970) 245-6933, or by electronic mail at fw6_
sagegrouse@fws.gov.
SUPPLEMENTARY INFORMATION:
Previous Federal Action
On January 18, 2000, the Director of the Service designated the
Gunnison sage-grouse as a candidate species under the Act, with a
listing priority of 5. The Federal Register notice regarding this
decision was not published until December 28, 2000 (65 FR 82310,
December 28, 2000). Candidates are species for which the Service has
determined that the species warrants listing as a threatened or
endangered species, but listing is precluded by higher listing
priorities for other species. A listing priority of 5 indicates that
there is a high magnitude of threats, but they are considered non-
imminent.
On January 26, 2000, The American Lands Alliance, Biodiversity
Legal Foundation, and others petitioned the Service to list the species
(Webb 2000). On January 10, 2001, some of the same plaintiffs sued the
Service alleging the Service had not made required petition findings.
In 2003, the U.S. District Court ruled that the Service's determination
that the Gunnison sage-grouse was a candidate constituted a 12-month
finding on the petition (American Lands Alliance v. Gale A. Norton,
C.A. No. 00-2339, (D.D.C., 2003).
The 2003 Candidate Notice of Review elevated the species' listing
priority number to 2 (69 FR 24876), as the imminence of the perceived
threats had increased. The 2004 Candidate Notice of Review (70 FR
24870) maintained the listing priority number as a 2.
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 includes a provision that the Service would make a listing
determination by March 31, 2006. On March 28, 2006, the plaintiffs
agreed to a one week extension (April 7, 2006) for this determination.
Section 4(b)(1)(A) of the Act requires us to consider the best
scientific and commercial data available as well as efforts being made
by States or other entities to protect a species when making a listing
decision. To meet this standard we collected information on the
Gunnison sage-grouse, its habitats, threats, and environmental factors
affecting the species from a wide array of sources. Most of the
available scientific literature on Gunnison sage-grouse is summarized
in the Gunnison Sage-grouse Rangewide Conservation Plan, a document
published in April 2005 under the auspices of the Gunnison Sage-grouse
Rangewide Steering Committee [GSRSC]. The GSRSC is comprised of
biologists from state and Federal agencies with responsibility for
managing the Gunnison sage-grouse or its habitat. The scientific
literature on Gunnison sage-grouse and its sagebrush habitats is
limited. Where information on Gunnison sage-grouse life history was
lacking, we used, as appropriate information on greater sage-grouse to
analyze habitat usage, threats, and environmental factors affecting the
Gunnison sage-grouse. In addition we received a substantial amount of
unpublished information from other Federal agencies, States, counties,
environmental organizations, and individuals. We also solicited
information on all Federal, State, or local conservation efforts
currently in operation or planned for the Gunnison sage-grouse or its
habitats.
In April 2005, Colorado Division of Wildlife (CDOW) applied to the
Service for a Gunnison sage-grouse Enhancement of Survival Permit
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). Public comments and other internal comments from the Service
and CDOW were incorporated into revisions of the CCAA and Environmental
Assessment; the documents are scheduled to be finalized shortly.
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. These participants provide
certain Gunnison sage-grouse 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 activities identified in
the Certificate of Inclusion. Although we strongly encourage continued
conservation of the Gunnison sage-
[[Page 19955]]
grouse, we did not rely upon this CCAA to support our listing
determination.
Species Information
In this determination, we use information specific to the Gunnison
sage-grouse where available. However, where such information is lacking
we use information on life history, habitat requirements, and effects
of threats on greater sage-grouse. Except where referenced, the
following life history information is taken from the Schroeder et al.
(1999) literature review on sage-grouse (Centrocercus spp.).
The sage-grouse is the largest grouse in North America and was
first described by Lewis and Clark in 1805 (Schroeder et al. 1999).
Sage-grouse 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).
For many years sage-grouse were considered a single species. Young
et al. (2000) identified Gunnison sage-grouse (Centrocercus minimus) as
a distinct species based on morphological (Hupp and Braun 1991; Young
et al. 2000), genetic (Kahn et al. 1999; Oyler-McCance et al. 1999),
and behavioral (Barber 1991; Young 1994; Young et al. 2000) differences
and geographical isolation. Based on these differences, the American
Ornithologist's Union (2000) accepted the Gunnison sage-grouse as a
distinct species. The current ranges of the two species are not
overlapping (Schroeder et al. 2004). We have considered the Gunnison
sage-grouse as a distinct species consistent with the petition under
review here. We acknowledge that there are questions regarding the
validity of this taxon, however it is not the purpose of this action to
elucidate taxonomic questions. The purpose of this action is to
determine the status of the taxon within the context of the ESA.
Gunnison sage-grouse and greater sage-grouse have similar life
histories and habitat requirements (Young 1994). Nesting success for
Gunnison sage-grouse is highest in areas where forbs and grass covers
are found below a sagebrush canopy cover of 15 to 30 percent (Young et
al. 2000). These numbers are comparable to those reported for the
greater sage-grouse (Connelly et al. 2000a). Connelly et al. (2000a)
also state that nest success for greater sage-grouse is greatest where
grass cover is present. Therefore, factors identified in the greater
sage-grouse literature that affect nesting habitat quality can affect
Gunnison sage-grouse nesting habitat in a similar manner if those
factors occur within the range of the Gunnison sage-grouse.
Characteristics of sage-grouse winter habitats are also similar through
the range of both species (Connelly et al. 2000a). 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; Young
et al. 2000). However, they may also use areas with more deciduous
shrubs during the winter (Young et al. 2000).
Dietary requirements of the two species also are similar, being
composed of nearly 100 percent sagebrush in the winter (Schroeder et
al. 1999; Young et al. 2000). Forbs and insects are important during
the summer and early fall. Gunnison and greater sage-grouse do not
possess muscular gizzards and, therefore, lack the ability to grind and
digest seeds (Rasmussen and Griner 1938; Leach and Hensley 1954).
Gunnison sage-grouse chick dietary requirements of insects and forbs
also are expected to be similar to greater sage-grouse and other grouse
species (Tony Apa, CDOW, pers. comm. 2005).
In the spring, sage-grouse gather on traditional breeding areas
referred to as leks (Patterson 1952). Lek displaying occurs from mid-
March through late May, depending on elevation (Rogers 1964). For
Gunnison sage-grouse, 87 percent of all nests were located less than 6
kilometers (km) (4 miles (mi)) from the lek of capture (Apa 2004). Mean
clutch size for Gunnison sage-grouse is 6.8 0.7 eggs
(Young 1994). Most eggs hatch in June, with a peak between June 10 and
June 20. Renesting rates following the loss of the original nest appear
very low in Gunnison sage-grouse, with one study reporting 4.8 percent
(Young 1994).
During the pre-egg laying period, female sage-grouse select forbs
that have generally higher amounts of calcium and crude protein than
sagebrush has (Barnett and Crawford 1994). Chicks are precocial and
leave the nest with the hen shortly after hatching. Females with chicks
move to areas containing succulent forbs and insects, often in wet
meadow habitat, where cover is sufficiently tall to conceal broods and
provide shade. 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;
Klebenow and Gray 1968; Peterson 1970; Johnson and Boyce 1990; Johnson
and Boyce 1991; Drut et al. 1994b; Pyle and Crawford 1996; Fischer et
al. 1996b). Diets of 4- to 8-week-old greater sage-grouse chicks were
found to have more plant material (Peterson 1970). 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;
Connelly and Markham 1983; Connelly et al. 1988; Fischer et al. 1996b).
During late summer and early fall, 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.
From late autumn through early spring the diet of greater and Gunnison
sage-grouse is almost exclusively sagebrush (Rasmussen and Griner 1938;
Batterson and Morse 1948; Patterson 1952; Leach and Hensley 1954;
Barber 1968; Wallestad et al. 1975; Young et al. 2000). Many species of
sagebrush can be consumed (Remington and Braun 1985; Welch et al. 1988,
1991; Myers 1992). Flock size in winter is variable (15 to 100+), and
flocks frequently consist of a single sex (Beck 1977; Hupp 1987).
During particularly severe winters, sage-grouse are dependent on tall
sagebrush, which is exposed even above deep snow, providing a
consistently available food source. In response to severe winters,
Gunnison sage-grouse have been documented to move as far as 27 km (17
mi) (Root 2002). 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. Movements in fall and
early winter (September-December) exceed 3 km (2 mi).
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). Higher survival rate of
female sage-grouse may be due to sexual dimorphism (Schroeder et al.
1999). 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). Other factors affecting
survival rates include year and age (Zablan 1993).
[[Page 19956]]
Habitat
Sage-grouse are sagebrush obligates (Patterson 1952; Connelly et
al. 2000a). They depend on a variety of shrub-steppe habitats
throughout their life cycle and are considered obligate users of
several species of sagebrush (Patterson 1952; Braun et al. 1976;
Schroeder et al. 1999; Connelly et al. 2000a; Connelly et al. 2004).
Sagebrush serves as a primary food for adults year-round (Wallestad et
al. 1975) and also provides cover for nests (Connelly et al. 2000a).
Sage-grouse move between seasonal ranges based on suitable habitat
availability. Connelly et al. (2000a) 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.
Breeding habitat includes leks and pre-laying, nesting, and early
brood-rearing areas. Male Gunnison sage-grouse attend leks from mid-
March to mid-May. Leks are typically in the same location from year to
year; some Gunnison sage-grouse leks have been used since the 1950s
(Rogers 1964). Leks are usually flat to gently sloping areas of less
than 15 percent grade in broad valleys or on ridges (Hanna 1936;
Patterson 1952; Giezentanner and Clark 1974; Wallestad 1975; Autenrieth
1981; Klott and Lindzey 1989). Leks have good visibility and low
vegetation structure (Tate et al. 1979; Connelly et al. 1981; Gates
1985), and acoustical qualities that allow sounds of breeding displays
to carry (Patterson 1952; Wiley 1973, 1974; Bergerud 1988; Phillips
1990). Leks are often surrounded by denser shrub-steppe cover, which is
used for escape, thermal, and feeding cover. Leks can be formed
opportunistically at any appropriate site within or adjacent to nesting
habitat (Connelly et al. 2000a) and, therefore, lek habitat
availability is not considered to be a limiting factor for sage-grouse
(Schroeder 1997). A relatively small number of dominant males accounts
for the majority of breeding on each lek (Schroeder et al. 1999).
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; Connelly et al. 2000a).
Nesting occurs from mid-April to June. Gunnison sage-grouse
typically select nest sites under sagebrush cover with some forb and
grass cover (Young 1994), and successful nests were found in higher
shrub density and greater forb and grass cover than unsuccessful nests
(Young 1994). The sagebrush 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; Connelly et al.
2000a; Connelly et al. 2004). Shrub canopy and grass cover provide
concealment for sage-grouse nests and young, and are critical for
reproductive success (Barnett and Crawford 1994; Gregg et al. 1994;
DeLong et al. 1995; Connelly et al. 2004). 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).
Young (1994) found that radio-tracked Gunnison sage-grouse nested
an average of 4.3 km (2.7 mi) from the lek nearest to their capture
site, with almost half nesting within 3 km (2 mi) of their capture
site. 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). Female sage-grouse have
been documented to travel more than 20 km (13 mi) to their nest site
after mating (Connelly et al. 2000a). Female Gunnison and greater sage-
grouse exhibit fidelity to nesting locations (Connelly et al. 1988;
Young 1994; Lyon 2000, Connelly et al. 2004, Holloran and Anderson
2005). 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; Connelly et al. 2004). However, there is no
statistical indication that movement to new nesting areas results in
increased nesting success (Connelly et al. 2004).
Early brood-rearing habitat is found close to nest sites (Connelly
et al. 2000a), although individual females with broods may move large
distances (Connelly 1982; as cited in Connelly et al. 2000a). Young
(1994) 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 hay
meadows, but were often flushed from interfaces of wet meadows and
habitats providing more cover, such as sagebrush or willow-alder
(Salix-Alnus). Forbs and insects are essential nutritional components
for sage-grouse chicks (Klebenow and Gray 1968; Johnson and Boyce 1991;
Connelly et al. 2004). Therefore, early brood-rearing habitat must
provide adequate cover adjacent to areas rich in forbs and insects to
assure chick survival during this period (Connelly et al. 2004).
As fall approaches sage-grouse move from riparian to upland areas
and start to shift to a winter diet (GSRSC 2005). By late summer and
into the early fall, individuals become more social, and flocks are
more concentrated (Patterson 1952). This is the period when Gunnison
sage-grouse can be observed in atypical habitat such as agricultural
fields (Commons 1997). However, radio-tracking studies in the Gunnison
Basin have found that broods typically do not use hay meadows further
away than 50 meters (m) (165 feet [ft]) of the edge of sagebrush stands
(Gunnison Basin Conservation Plan 1997).
Movements to winter ranges are slow and meandering. Sagebrush stand
selection in winter is influenced by snow depth (Patterson 1952;
Connelly 1982 as cited in Connelly et al. 2000a) and in some areas,
topography (Beck 1977; Crawford et al. 2004). 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)
associated with drainages, ridges, or southwest aspects with slopes
less than 15 percent (Wallestad 1975; Beck 1977). 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 roosts'' (Back et al. 1987).
Hupp and Braun (1989) 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. In these
conditions, the tall and vigorous sagebrush typical in drainages was an
especially important food source.
Historical Distribution
Based on historical records, museum specimens, and potential sage-
grouse habitat, Schroeder et al. (2004) concluded that Gunnison sage-
grouse historically occurred in southwestern Colorado, northwestern New
Mexico, northeastern Arizona, and southeastern Utah. Accounts of
Gunnison sage-grouse in Kansas and Oklahoma, as suggested by Young et
al. (2000), are not
[[Page 19957]]
supported with museum specimens, and Schroeder et al. (2004) found
inconsistencies with the historical records and the sagebrush habitat
currently available in those areas. Applegate (2001) 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). The GSRSC (2005) modified the historic range from Schroeder et
al. (2004), based on more complete knowledge of historic and current
habitat and the distribution of the species (GSRSC 2005). Based on this
information, the maximum Gunnison sage-grouse historical
(presettlement) range is estimated to have been 55,350 square
kilometers (sq km) (21,370 square miles [sq mi]) (GSRSC 2005). 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 occupied,
or what the total population was.
Rogers (1964) qualitatively discussed a decrease in sagebrush range
due to overgrazing from the 1870's until about 1934. Additional 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 (Rogers 1964). Rogers
(1964) discussed sagebrush eradication (by spraying and burning) in the
1950s, and used two examples (Uncompaghre Plateau, Flattop Mountain in
Gunnison County, CO) within the current range to illustrate the large
acreages (3-5,000 acres) treated, but stated that long-term effects
were yet to be determined. Rogers (1964) demonstrated a much broader
distribution of sagebrush in Colorado than what currently exists.
Rogers (1964) also presents maps that show decreases in distribution
from previous literature.
Much of what was once sagebrush was already lost prior to 1958.
Through the use of low-level aerial photography, Oyler-McCance et al.
(2001) documented a loss of only or 155,673 ha (20 percent) of
sagebrush habitat from 1958 to 1993 within Gunnison sage-grouse range.
Thirty-seven percent of the plots sampled underwent substantial
fragmentation of sagebrush vegetation during that same time period.
Oyler-McCance et al. (2001) stated that sage-grouse habitat in
southwestern Colorado (the range of Gunnison sage-grouse) has been more
severely impacted than sagebrush habitat elsewhere in Colorado.
However, the Gunnison Basin was not as significantly affected as other
areas.
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 throughout the range of Gunnison sage-grouse.
Riebsame et al (1996) discussed a greater rural growth rate in
Colorado from the 1970s through the 1990s, compared to the rest of the
U.S., which has resulted in land use conversion. They noted a pattern
of private ranches shifting to residential communities within Gunnison
sage-grouse habitat. The Gunnison Basin Working Group Research Sub-
committee (February, 2006) cited two regions within the Basin to be of
the highest priority for conservation easements due to development
pressures.
In summary, a substantial amount of sagebrush habitat within the
range of the Gunnison sage-grouse had been lost prior to 1960. In the
years since, habitat loss and fragmentation has slowed, although
development pressures have been on the rise. Conservation efforts are
being developed to help address development-related issues.
Current Distribution and Population Estimates
Gunnison sage-grouse currently occur in seven widely scattered and
isolated populations in Colorado and Utah, occupying 4,720 sq km (1,820
sq mi) (GSRSC 2005). The seven populations are Gunnison Basin, San
Miguel Basin, Monticello-Dove Creek, Pi[ntilde]on Mesa, Crawford, Cerro
Summit-Cimarron-Sims Mesa, and Poncha Pass (Figure 1). A comparative
summary of the seven populations is presented in Table 1.
[[Page 19958]]
[GRAPHIC] [TIFF OMITTED] TR18AP06.000
[[Page 19959]]
Table 1.--Population Size, Extent of Occupied Habitat, Land Ownership, and Urban Development Pressures
--------------------------------------------------------------------------------------------------------------------------------------------------------
Population size 2005 population Currently occupied
Name of population range 1995-2005* estimate area Land ownership Development pressure
--------------------------------------------------------------------------------------------------------------------------------------------------------
Gunnison Basin Population........ 2,203-4,763......... 4,763............... 240,000 hectares 51 percent BLM, 14 Gunnison County
(ha) 593,000 (ac). percent USFS, 2 percent currently has a low
NPS, 1 percent CDOW, 1 population density of 5
percent Colorado State people/sq mi in 2000
Land Board, 31 percent (GSRSC 2005), with
private (GSRSC 2005). projected growth rates
ranging from .1 to 1.6
percent per year. These
rates result in a
population increase of
about 5700 people by
2030 (41 percent or 7
people/sq mi) (CDLA
2004). A 30 percent
housing increase is
projected from 2000-
2020 (GSRSC 2005).
--------------------------------------------------------------------------------------------------------------------------------------------------------
San Miguel Basin Population...... 206-446............. 334................. 40,500 ha (100,500 Dry Creek--57 percent The population in San
ac). BLM, 12 percent, CDOW, 1 Miguel County is
percent, Colorado State expected to double to
Land Board, 30 percent 18 people/sq mi between
private. 2000 and 2030 (CDLA
Hamilton Mesa--85 percent 2004), accompanied by a
private, 11 percent 62 percent increase in
Colorado State Land housing units by 2020
Board, 4 percent BLM. (GSRSC 2005).
Miramonte--76 percent
private, 15 percent
CDOW, 7 percent USFS, 2
percent BLM.
Gurley Reservoir--91
percent private, USFS 4
percent, BLM 3 percent,
the Colorado State Land
Board 2 percent.
Beaver Mesa--99.5 percent
private, 0.5 percent BLM.
Iron Springs--89 percent
private, 6 percent USFS,
5 percent Colorado State
Land Board (GSRSC 2005).
--------------------------------------------------------------------------------------------------------------------------------------------------------
Monticello-Dove Creek Population. 162-510 (Combined).. 196 (162 Monticello 40,000 ha (98,920 Monticello--95 percent The Monticello, UT group
and 34 Dove Creek). ac) (Combined). private, 4 percent BLM, has approximately 2
1 percent State of Utah people/sq mi (GSRSC
land. 2005) with a projected
increase of roughly 18%
to 2600 people (2.4
people/sq mi) by 2030
(Utah Governor's Office
of Planning and Budget
2005).
123-280 (Monticello) .................... Monticello--28,500 Dove Creek--87 percent
ha (71,000 ac). privately owned, 13
percent BLM (GSRSC 2005).
10-358 (Dove Creek). .................... Dove Creek--11,500
ha (28,000 ac).
--------------------------------------------------------------------------------------------------------------------------------------------------------
Pi[ntilde]on Mesa Population..... 79-206.............. 167................. 16,000 ha (39,000 70 percent private, 28 Population density of 55
ac). percent BLM, 2 percent people/sq mi in 2000
USFS (GSRSC 2005). (GSRSC 2005) with a
projected increase to
105 people/sq mi by
2030 (CDLA 2004).
--------------------------------------------------------------------------------------------------------------------------------------------------------
[[Page 19960]]
Crawford Population.............. 118-314............. 191................. 14,000 ha (35,000 63 percent BLM, 13 Estimate of 24 people/sq
ac). percent NPS, 24 percent mi living in and near
private (GSRSC 2005). this population in 2000
(GSRSC 2005). Montrose
County contains the
southeastern 75 percent
of the current range of
the Crawford
population. The county
was identified as one
of the fastest growing
counties in the
country, with human
population expected to
double from 2000-2030
(CDLA 2004) and housing
expected to increase by
68 percent by 2020. The
northwestern 25 percent
of the current range is
in Delta County, which
is projected to
increase in population
by 79 percent by 2030
(CDLA 2004) with an
increase in housing of
58 percent by 2020
(GSRSC 2005).
--------------------------------------------------------------------------------------------------------------------------------------------------------
Cerro Summit-Cimarron-Sims Mesa 25-83............... 25.................. 15,000 ha (37,000 43 percent private, 51 Population threats not
Population. ac). percent BLM, 6 percent evaluated.
CDOW (GSRSC 2005).
Poncha Pass Population........... 5-44................ 44.................. 8,300 ha (20,400 ac) 48 percent BLM, 26 Population threats not
percent USFS, 24 percent evaluated.
in private holdings, 2
percent Colorado State
Land Board (GSRSC 2005).
--------------------------------------------------------------------------------------------------------------------------------------------------------
* The numbers presented are the lowest and highest population estimates during the 11-year period. The lows and highs did not all fall in the same years
for each population.
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). Big sagebrush (Artemesia tridentata) dominates the upland
vegetation and has a highly variable growth form depending on local
site conditions. Up to 84 leks have been surveyed annually for breeding
activity in the Gunnison Basin (CDOW, unpubl. lit. 2005a).
Approximately 37 percent of these leks occur on private land and 63
percent on public land, primarily BLM (GSRSC 2005). In 2005, 44 of
these leks were active, 38 inactive, and 2 are of unknown status.
Rogers (1964) stated that Gunnison County had one of the largest sage-
grouse populations in Colorado.
San Miguel Basin Population--The San Miguel Basin population is in
Montrose and San Miguel Counties in Colorado, and is composed of six
groups using different areas--Dry Creek Basin, Hamilton Mesa, Miramonte
Reservoir, Gurley Reservoir, Beaver Mesa, and Iron Springs. Some of
these six areas are used year-round by sage-grouse, and others are used
seasonally. Recent radiotelemetry studies have suggested that sage-
grouse in the San Miguel Basin move widely and between these areas (Apa
2004; Stiver, unpubl. lit. 2005).
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). Gunnison sage-grouse use the Hamilton Mesa area in the
summer, but use during other seasons is unknown. Miramonte Reservoir
occupied sage-grouse habitat is approximately 4,700 ha (11,600 ac)
(GSRSC 2005). Sagebrush stands are generally contiguous with a mixed
grass and forb understory. Occupied habitat at the Gurley Reservoir
area is heavily fragmented 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 now
are restricted primarily to the seasonal irrigation 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). Sagebrush stands in the Iron Springs
and Beaver Mesa areas are contiguous with a mixed grass understory. The
Beaver Mesa area has numerous scattered patches of oakbrush (Quercus
gambelii).
The 2005 population estimate for the entire San Miguel Basin was
334 (CDOW, unpubl. lit. 2005b) on 9 leks. Rogers (1964) reported that
all big sagebrush-dominated habitats in San Miguel and Montrose
Counties were historically used by sage-grouse. The historic
distribution was highly fragmented by forests, rocky canyons and dry
basins void of sagebrush habitats.
[[Page 19961]]
Monticello-Dove Creek Population--This population has two disjunct
groups of Gunnison sage-grouse. Currently, the largest group is near
the town of Monticello, Utah. Gunnison sage-grouse in this group
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) estimates that Gunnison sage-grouse currently occupy
about 24,000 ha (60,000 ac) in the Monticello group. The 2005
population estimate for Monticello was 162 individuals with 2 active
and 2 inactive leks (G. Wallace, UDWR pers. comm. 2005). Leks in the
Monticello area were first identified and counted in 1968.
The Dove Creek group 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 7
males in 2005 (CDOW, unpubl. lit. 2005c). All leks are located in
agricultural fields on private lands. 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; Apa
2004). Rogers (1964) reported that all sagebrush-dominated habitats in
Dolores and Montezuma Counties within Gunnison sage-grouse range in
Colorado were historically used by sage-grouse.
Pi[ntilde]on Mesa Population--The Pi[ntilde]on Mesa population
occurs on the northwest end of the Uncompahgre Plateau in Mesa County,
about 35 km (22 mi) southwest of Grand Junction, Colorado. Eight leks
are known (CDOW, unpubl. lit. 2004). However, one is inactive and
another was not active in 2005 (CDOW unpubl. lit. 2005d). The
Pi[ntilde]on Mesa area may have additional leks, but the high
percentage of private land, a lack of roads, and heavy snow cover
during spring makes locating additional leks difficult. Gunnison sage-
grouse likely occurred historically in all suitable sagebrush habitat
in the Pi[ntilde]on Mesa area, including the Dominguez Canyon area of
the Uncompaghre Plateau, southeast of Pi[ntilde]on Mesa proper (Rogers
1964). Their current distribution has been substantially reduced from
historic levels (GSRSC 2005).
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 (A. t. tridentata) and black sagebrush (A. nova) dominate the
mid-elevation uplands (GSRSC 2005). The 2005 population estimate for
Crawford is 191 (CDOW, unpubl. lit. 2005e). Currently there are four
active leks 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).
Cerro Summit-Cimarron-Sims Mesa Population--This population is in
Montrose County, Colorado. The Cerro Summit-Cimarron group is centered
about 24 km (15 mi) east of Montrose. The habitat consists of patches
of sagebrush habitat fragmented by oakbrush and irrigated pastures.
Three leks are known in the Cerro Summit-Cimarron group, but only one
was verified to be active in 2005. Rogers (1964) 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 is inactive. Rogers (1964) counted eight
males in a lek count at Sims Mesa in 1960. It is not known if sage-
grouse move between the Cerro-Summit-Cimarron and Sims Mesa groups.
Poncha Pass Population--The Poncha Pass sage-grouse population is
located in Saguache County, approximately 16 km (10 mi) northwest of
Villa Grove, Colorado. This population was established through the
introduction of 30 birds from the Gunnison Basin in 1971 and 1972
during efforts to reintroduce the species to the San Luis Valley (GSRSC
2005). The known population distribution is in 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 extensive
and continuous with little fragmentation; sagebrush habitat quality
throughout the area is adequate (Nehring and Apa 2000). San Luis Creek
runs through the area, providing a year-round water source and lush,
wet meadow riparian habitat for brood-rearing. The 2005 Poncha Pass
sage-grouse population estimate is 44 (CDOW, unpubl. lit. 2005f). 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 transplanted 24 additional birds from the Gunnison
Basin (Nehring and Apa 2000). In 2001 and 2002, 20 and 7 birds
respectively also were moved to the Poncha Pass by CDOW (GSRSC 2005).
Transplanted females have bred successfully (Apa, CDOW, pers. comm.
2004) and display activity resumed on the historic lek in spring 2001.
Population Trends
Trends in abundance were analyzed for individual populations and
the species rangewide using male lek count data from CDOW and UDWR
(Garton 2005). Due to inconsistencies in data collection over time,
trend analyses were conducted for two time periods--the entire number
of years lek data have been collected (1957-2005), and from 1995-2005
when sampling methodologies have been more consistent. Raw data
collected for 2005 show a large increase in the numbers of males
attending leks. Because of this, the analyses were conducted both with
and without 2005 data; estimates did not change significantly when the
2005 lek counts were omitted in this analysis. Statistical analyses of
the Cerro Summit-Cimarron-Sims Mesa and Dove Creek populations could
not be completed due to low lek counts and inconsistencies in sampling
over time. Similarly, the small Poncha Pass population was not analyzed
because it has been surveyed for only 6 years and in that time the
population was augmented with birds from Gunnison Basin.
The long-term analysis (1957-2005) found that the rangewide
population of Gunnison sage-grouse was neither increasing nor
decreasing during that time period. Annual rates of change were highly
variable, most likely as a result of sampling error rather than actual
changes in population sizes. The shorter analysis period (1995-2005)
yielded the same results, although the variability was reduced, likely
due to more consistent data collection methods. Individual populations
reflected the trends in the rangewide analysis, in that some
populations were slightly increasing and some were slightly decreasing
(Table 2). As with similar analyses conducted for the
[[Page 19962]]
greater sage-grouse (Connelly et al. 2004), density-dependent models
appeared to more accurately describe observed population trends (Garton
2005).
Table 2.--Summary of Population Trends for the Gunnison Sage-Grouse \1\
------------------------------------------------------------------------
Finite
rate
Population of
change
------------------------------------------------------------------------
Rangewide....................................................... 1.049
Gunnison Basin.................................................. 1.05
Pi[ntilde]on Mesa............................................... 1.09
San Miguel Basin................................................ 0.9
Crawford........................................................ 0.999
Monticello...................................................... 0.99
------------------------------------------------------------------------
\1\ Values are the finite rate of change in the population, where 1 is
no change, numbers less than 1 indicate a decline, and numbers greater
than 1 indicate an increase. The analysis is for 1995-2005 (data from
Garton 2005).
Because we relied on the population trend analyses conducted by
Garton (2005), we asked six peer reviewers to evaluate the report. We
received comments from five of the reviewers, three generally favorable
towards the report and its conclusions and two expressing concerns
regarding limitations in the data sets, assumptions, and/or analyses.
For example, one would have to assume that habitat availability over
time would remain stable in order to conclude that Gunnison sage-grouse
numbers are unlikely to experience a substantial decline in the future.
Also, while the conclusions showed that the number of males per lek
remained relatively stable over time, the proportion of leks on which
males were counted appeared to have declined, which could be indicative
of an overall population decline. In discussing the historic
distribution of Gunnison sage-grouse, we concluded that much of the
habitat loss, and by inference population decline, occurred prior to
1958.
It was also suggested that more appropriate statistical tests would
need to be applied to come to any conclusion about potential population
trends and that emphasis should be on an independent analysis of each
geographically isolated population because each population exhibits
independent population dynamics. Population trend analyses were
conducted on a population basis (as well as rangewide). However, to
further subdivide the data analyzed into smaller units (i.e.
subpopulations) would have compromised the statistical integrity of the
analysis due to small sample sizes. There was concern expressed that
habitat loss over time was not accounted for, that population declines
would go unnoticed, and that population trends would appear far too
optimistic.
An identical population trend analysis was peer reviewed by the
Ecological Society of America in the ``Conservation Assessment of
Greater Sage-grouse and Sagebrush Habitats'' (Connelly et al. 2004).
Additional clarifying information regarding model assumptions, the
primary concern of the peer reviewers, was provided by Garton after the
peer review was complete. Based on this late submission, and after
careful review of the analysis, we believe that Garton (2005)
constitutes the best currently available information.
Summary of Factors Affecting the Species
Section 4 of the Act (16 U.S.C. 1533) and regulations (50 CFR part
424) promulgated to implement the listing provisions of the Act set
forth the procedures for adding species to the Federal lists. A species
may be determined to be an endangered or threatened species due to one
or more of the five factors described in section 4(a)(1). As part of
our analysis, we chose, out of an abundance of caution, not to rely on
the Cerro Summit-Cimarron-Sims Mesa and Poncha Pass populations and the
Dove Creek group of the Monticello-Dove Creek population for the
longterm conservation of the species because of their small, isolated
status. We also determined that these populations do not comprise a
significant portion of the Gunnison sage-grouse range. Therefore, these
populations/group were not evaluated further for future threats.
Although we are not relying on these populations/group for the longterm
conservation of the species, we nonetheless believe that conservation
of these populations is worthwhile, and we will continue to support and
encourage those efforts. However, we analyze the threats applicable to
the remaining populations/group to determine whether the species as a
whole meets the definition of threatened or endangered.
The Service considers the foreseeable future in Gunnison sage-
grouse to be between 30 and 100 years based on 10 Gunnison sage-grouse
generations to 2 sagebrush habitat regeneration cycles. This is
consistent with our 12-month finding for the greater sage-grouse (70 FR
2244). Because the Gunnison sage-grouse has the same generation time
and occupies habitat similar to the greater sage-grouse, we consider it
prudent to use the same definition for the foreseeable future.
A. The Present or Threatened Destruction, Modification, or Curtailment
of Its Habitat or Range
Data indicate that the Gunnison sage-grouse was found in central
and southwest Colorado, southeast Utah, northwestern New Mexico, and
northeastern Arizona prior to European settlement (GSRSC 2005, modified
from Schroeder et al. 2004). Gunnison sage-grouse currently occupy
4,719 sq km (1,822 sq mi) in southwestern Colorado and southeastern
Utah (GSRSC 2005, modified from Schroeder et al. 2004). The following
describes the issues affecting Gunnison sage-grouse within their
current range.
Current Threats Due to Habitat Fragmentation: Habitat fragmentation
is the separation or splitting apart of previously contiguous,
functional habitat. Fragmentation of sagebrush habitats has been cited
as a primary cause of the decline of sage-grouse populations (Patterson
1952; Connelly and Braun 1997; Braun 1998; Johnson and Braun 1999;
Connelly et al. 2000a; Miller and Eddleman 2000; Schroeder and Baydack
2001; Aldridge and Brigham 2003; Connelly et al. 2004; Schroeder et al.
2004). While sage-grouse are dependent on interconnected expanses of
sagebrush (Patterson 1952; Connelly et al. 2004), data are not
available regarding optimum or even minimum sagebrush patch sizes
necessary to support sage-grouse populations. In addition, there is a
lack of data to assess how fragmentation influences specific sage-
grouse life-history parameters such as productivity, density, and home
range.
Oyler-McCance et al. (2001) documented loss and fragmentation of
sagebrush vegetation in southwestern Colorado. In a genetic study of
Gunnison sage-grouse populations, Oyler-McCance et al. (2005) concluded
that gene flow among populations of Gunnison sage-grouse is limited.
Notwithstanding the lack of specificity on effects of
fragmentation, it is clear that as a whole, fragmentation can have an
adverse effect on sage-grouse populations. The following sections
examine activities that can contribute to habitat fragmentation to
determine whether they threaten Gunnison sage-grouse habitat.
Conversion to Agriculture and Water Development
In the mid-1800s, western rangelands were converted to agricultural
lands on a large scale beginning with the series of Homestead Acts in
the 1800s (Braun 1998; Hays et al. 1998), especially where suitable
deep soil terrain and
[[Page 19963]]
water were available (Rogers 1964). Influences resulting from
agricultural activities adjoining sagebrush habitats extend into those
habitats, and include increased predation and reduced nest success due
to predators associated with agriculture (Connelly et al. 2004).
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 sage-grouse (C.
Braun, CDOW, pers. comm. 1998). However, crop monocultures do not
provide adequate year-round food or cover (GSRSC 2005). Gunnison sage-
grouse will use hay pastures for foraging within about 50 m (165 ft) of
the edge of the field but do not forage further into the pasture due to
lack of suitable habitat (Gunnison Basin Conservation Plan 1997).
In the Gunnison Basin approximately 17,328 ha (42,800 ac) or 8
percent of the current range was converted to agricultural activities
in the past and for the most part is no longer occupied (GSRSC 2005).
Approximately 5,700 ha (14,000 ac) or 7 percent of the current range in
the San Miguel Basin has been converted to agriculture and for the most
part is unoccupied (GSRSC 2005). The arrangement of these converted
lands has contributed to habitat fragmentation in these areas, although
it is not negatively influencing sage-grouse numbers in this population
(Garton 2005).
Approximately 30 percent of the 40,048 ha (98,920 ac) of the
current range in the Monticello-Dove Creek population has been
converted to agriculture and for the most part is no longer occupied
(GSRSC 2005). In the Monticello group, 43 percent has been converted to
pasture (GSRSC 2005). San Juan County, Utah, where the Monticello group
resides, also has approximately 15,000 ha (37,000 ac) enrolled in
Conservation Reserve Program (CRP), of which about half is within
current sage-grouse range (San Juan County Gunnison Sage-grouse Work
Group [GSWG], unpubl. lit. 2005; GSRSC 2005). Under CRP, cropland is
planted to pastureland and, except in emergency situations, not hayed
or grazed. The CRP fields are used heavily by grouse as brood-rearing
areas but vary greatly in plant diversity and forb abundance, and
generally lack any shrub cover (GSRSC 2005). Sagebrush patches have
progressively become smaller and more fragmented limiting the amount of
available winter habitat for the Monticello group (GSRSC 2005).
Significant use of CRP as nesting or winter habitat will require
establishment of sagebrush stands in these fields. The CRP has
protected this area from more intensive agricultural use and
developme