Endangered and Threatened Wildlife and Plants; 12-month Finding on a Petition to List the White-tailed Prairie Dog as Endangered or Threatened, 30338-30363 [2010-12599]
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DEPARTMENT OF THE INTERIOR
Fish and Wildlife Service
In accordance with the President’s
memorandum of April 29, 1994,
‘‘Government-to-Government Relations
with Native American Tribal
Governments’’ (59 FR 22951), Executive
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readily acknowledge our responsibility
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have determined that there are no tribal
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in this rule is available on the Internet
at https://www.regulations.gov, or upon
request from the Field Supervisor, Ohio
Field Office (see FOR FURTHER
INFORMATION CONTACT).
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(see FOR FURTHER INFORMATION CONTACT).
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Endangered and threatened species,
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Accordingly, we propose to amend
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as follows:
PART 17—[AMENDED]
1. The authority citation for part 17
continues to read as follows:
Authority: 16 U.S.C. 1361-1407; 16 U.S.C.
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2. Amend §17.11 (h) by removing the
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Dated: May 17, 2010
Gregory E. Siekaniec
Acting Director, Fish and Wildlife Service
[FR Doc. 2010–12910 Filed 5–28–10; 8:45 am]
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50 CFR Part 17
[Docket No. FWS-R6-ES-2008-0053]
[MO 92210-0-0008-B2]
Endangered and Threatened Wildlife
and Plants; 12–month Finding on a
Petition to List the White-tailed Prairie
Dog as Endangered or Threatened
AGENCY: Fish and Wildlife Service,
Interior.
ACTION: Notice of a 12–month petition
finding.
SUMMARY: We, the U.S. Fish and
Wildlife Service announce a 12–month
finding on a petition to list the whitetailed prairie dog (Cynomys leucurus) as
endangered or threatened under the
Endangered Species Act of 1973, as
amended. After a review of all available
scientific and commercial information,
we find that listing the white-tailed
prairie dog is not warranted at this time.
However, we ask the public to submit to
us any new information that becomes
available concerning the threats to the
white-tailed prairie dog or its habitat at
any time.
DATES: The finding announced in this
document was made on June 1, 2010.
ADDRESSES: This finding is available on
the Internet at https://
www.regulations.gov at Docket Number
FWS-R6-ES-2008-0053. Supporting
documentation we used in preparing
this finding is available for public
inspection, by appointment, during
normal business hours at the U.S. Fish
and Wildlife Service, Utah Field Office,
2369 West Orton Circle, Suite 50, West
Valley City, UT 84119. Please submit
any new information, materials,
comments, or questions concerning this
finding to the above street address.
FOR FURTHER INFORMATION CONTACT:
Larry Crist, Field Supervisor, Utah Field
Office (see ADDRESSES); by telephone at
801-975-3330; or by facsimile at 801975-3331. If you use a
telecommunications device for the deaf
(TDD), please call the Federal
Information Relay Service (FIRS) at 800877-8339.
SUPPLEMENTARY INFORMATION:
Background
Section 4(b)(3)(B) of the Endangered
Species Act of 1973, as amended (Act)
(16 U.S.C. 1531 et seq.), requires that,
for any petition to revise the Federal
Lists of Endangered and Threatened
Wildlife and Plants that contains
substantial scientific or commercial
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information that listing the species may
be warranted, we make a finding within
12 months of the date of receipt of the
petition. In this finding, we will
determine that the petitioned action is:
(1) Not warranted, (2) warranted, or (3)
warranted, but the immediate proposal
of a regulation implementing the
petitioned action is precluded by other
pending proposals to determine whether
species are endangered or threatened,
and expeditious progress is being made
to add or remove qualified species from
the Federal Lists of Endangered and
Threatened Wildlife and Plants. Section
4(b)(3)(C) of the Act requires that we
treat a petition for which the requested
action is found to be warranted but
precluded as though resubmitted on the
date of such finding, that is, requiring a
subsequent finding to be made within
12 months. We must publish these 12–
month findings in the Federal Register.
Previous Federal Action
On July 15, 2002, we received a
petition dated July 11, 2002, from the
Center for Native Ecosystems, Forest
Guardians, Biodiversity Conservation
Alliance, and Terry Tempest Williams,
requesting that the white-tailed prairie
dog (Cynomys leucurus) be listed as
endangered or threatened across its
entire range. We acknowledged the
receipt of the petition in a letter to the
petitioners, dated August 27, 2002. In
that letter we also stated that higher
priority actions precluded addressing
the petition immediately, but it would
be addressed when funding allowed.
Section 4(b)(3)(B) of the Act requires
that for any petition to revise the Lists
of Threatened and Endangered Wildlife
and Plants, to the maximum extent
practicable, within 90 days after
receiving the petition, we make a
finding as to whether the petition
presents substantial scientific or
commercial information indicating that
the petitioned action may be warranted.
On November 9, 2004, we announced
our 90–day finding (69 FR 64889) that
the petition did not present substantial
scientific or commercial information
indicating that listing may be warranted.
On July 12, 2007, in a Director’s
memorandum, the U.S. Fish and
Wildlife Service (Service) announced
that we would review the November 9,
2004, finding after questions were raised
about the integrity of scientific
information used and whether the
decision was consistent with the
appropriate legal standards. We
received notice of a lawsuit from the
Center for Native Ecosystems, and three
other entities, on November 27, 2007,
regarding our not-substantial 90–day
finding. We agreed in a stipulated
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settlement agreement on February 22,
2008, to submit a notice initiating a 12–
month finding for the white-tailed
prairie dog to the Federal Register on or
before May 1, 2008, and to submit a 12–
month finding for the white-tailed
prairie dog to the Federal Register on or
before June 1, 2010. Due to the
stipulated settlement agreement, the
petitioners dismissed the lawsuit on
February 26, 2008. This notice
constitutes the 12–month finding under
the stipulated settlement agreement on
the petition to list the white-tailed
prairie dog as endangered or threatened.
Species Information
Species Description
White-tailed prairie dogs are between
340 to 370 millimeters (mm) (13.4 to
14.6 inches (in)) in length with a 40- to
65-mm (1.6- to 2.6-in) long tail (Clark et
al. 1971, p. 1). The tail has a grayish
white tip and is white on the terminal
half. The coat is generally yellow-tan
with distinctive dark brown or black
cheek patches that extend above the eye
with a lighter black stripe that extends
below the eye onto the cheek (Clark et
al. 1971, p. 1).
Taxonomy
The white-tailed prairie dog is one of
five prairie dog species that inhabit
western North America (Clark et al.
1971, p. 1; Pizzimenti 1975, pp. 62-63).
Prairie dogs are in the squirrel family,
Sciuridae, and belong to the genus
Cynomys (Hollister 1916, p. 5). The
genus is split into two subgenera;
Leucocrossuromys includes prairie dogs
with white tails and Cynomys includes
prairie dogs with black tails. Whitetailed prairie dogs are included in the
subgenus Leucocrossuromys along with
Utah and Gunnison prairie dogs (Clark
et al. 1971, p. 1; Pizzimenti 1975, pp.
15-16). Due to this consensus, we
determined that the white-tailed prairie
dog is a valid taxonomic species and a
listable entity under the Act.
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Ecology and Life History
White-tailed prairie dogs occur at
elevations ranging from 1,150 meters
(m) (3,773 feet (ft)) (Flath 1979, p. 63)
to 3,200 m (10,500 ft) (Tileston and
Lechleitner 1966, p. 295). Unlike the
grass-dominated habitats of black-tailed
prairie dogs, white-tailed prairie dogs
inhabit drier landscapes with shrubland
vegetation (Tileston and Lechleitner
1966, p. 295; Clark 1977, pp. 3-5;
Collins and Lichvar 1986, pp. 88-91;
Gadd 2000, pp. 15-16). Their habitats
are generally flat (Collins and Lichvar
1986, p. 92).
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Prairie dogs are primarily herbivorous
and mainly eat grasses and forbs (Kelso
1939, pp. 7-11). However, they consume
other plants seasonally. Prairie dog
selection of plants is somewhat
dependent on site-specific conditions
and seasonality. For example, whitetailed prairie dogs eat sagebrush and
saltbush during early spring, grasses in
the summer, and seed heads and
rabbitbrush flowers in the fall (Kelso
1939, p. 10; Tileston and Lechleitner
1966, p. 302). White-tailed prairie dogs
eat the least amount of grass of any
prairie dog species and the most
saltbush (Kelso 1939, p. 11). Whitetailed prairie dogs also eat insects
(Stockard 1929, p. 476). Prairie dogs
obtain most of their water by eating
vegetation and can become waterstressed if sufficient succulent
vegetation is unavailable (Seglund et al.
2006, p. 7).
White-tailed prairie dogs prefer areas
with lower vegetation heights (Collins
and Lichvar 1986, p. 92), but they may
use dense sagebrush adjacent to grassier
areas (Tileston and Lechleitner 1966, p.
314). White-tailed prairie dogs use the
dense vegetation within sagebrush
habitat to hide from predators
(Hoogland 1981, pp. 266-268; Gadd
2000, pp. 24-26), reducing their need to
visually search for predators and
consequently reducing their need for
dense colonies and cohesive social
structures. This habitat use differs from
black-tailed prairie dogs, who actively
work to maintain the grassland
vegetation surrounding their burrows
for visibility.
White-tailed prairie dogs dig their
own burrows. Burrow construction
requires deep, well-drained soils.
Preferred soils are derived from
sandstone or shale and may be clayloam, silty clay, or sandy loam (Lupis et
al. 2007, p. 6). Burrows are used
throughout the year for hibernation,
cover from temperature extremes,
predator avoidance, and birthing and
raising young (Clark 1977, p. 9;
Hoogland 1981, pp. 258-264). Burrow
complexes are usually widespread with
numerous entrances, tunnels, and
chambers. The number of burrows in an
area varies greatly from location to
location, ranging from 0.12 to 47.75 per
hectare (ha) (0.3 to 118 per acre (ac))
with a mean of 0.32 to 6.79 per ha (0.8
to 16.8 per ac) (Tileston and Lechleitner
1966, p. 314; Menkens and Anderson
1989, p. 84; Seglund and Schnurr 2009,
p. 94).
For purposes of this finding, a group
of burrows is referred to as a colony. A
complex is a collection of colonies
grouped on the landscape. There is
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usually a high degree of connectivity
between colonies in the same complex.
White-tailed prairie dog colonies have
fewer animals per unit area with less
obvious borders than black-tailed prairie
dog colonies (Tileston and Lechleitner
1966, pp. 297, 314; Hoogland 1981, p.
252). Home range sizes range from 0.2
to 1.9 ha (0.5 to 4.7 ac) (Clark 1977, p.
65; Cooke 1993, p. 23), which are
generally larger than black-tailed prairie
dog home ranges (Clark 1977, p. 65).
White-tailed prairie dogs can live up
to 8 years in captivity but may not live
past 4 years in the wild (Pauli et al.
2006, p. 18). Prairie dog annual
mortality rates average 30 to 60 percent,
largely due to disease and predation
(Tileston and Lechleitner 1966, p. 305;
Clark 1977, pp. 80-81).
Adult sex ratios are approximately
one male to two females (Clark 1977, p.
76; Hoogland 2010, pers. comm.).
White-tailed prairie dogs can reproduce
at 1 year of age, and they have a single
litter once a year averaging four to five
pups (Bakko and Brown 1967, pp. 110111). Breeding occurs from late March
to mid-April (Tileston and Lechleitner
1966, p. 303). Pups are born in the
burrows after a gestation period of
approximately 30 days (Tileston and
Lechleitner 1966, p. 304), and emerge
from the burrow for the first time 4 to
6 weeks after birth (Bakko and Brown
1967, p. 103). They begin to disperse
from the colony in June and July when
population densities are the highest
(Clark 1977, p. 72). Migration is
recognized as an important factor to
white-tailed prairie dog population
dynamics (Clark 1977, p. 80). Plague in
this species often results in near
extirpation of colonies. Rapid
recolonization of some areas post-plague
with few or no surviving reproductive
adults suggests the species is highly
mobile (Seglund et al. 2006, p. 10).
Dispersal distances of up to 8 kilometers
(km) (4.8 miles (mi)) have been observed
(Cooke 1993 in Seglund et al. 2006, p.
10)
White-tailed prairie dogs have the
least cohesive social structure of any
prairie dog species. Their social system
is organized around family groups or
‘‘clans,’’ comprised of several
reproductive females, one or two males
of reproductive age, and dependent
young (Clark 1977, p. 62; Cooke 1993,
p. 22). Adult white-tailed prairie dogs
spend little time displaying social
behavior, and most of their time feeding
or in alert postures (Clark 1977, p. 44).
Pups spend a large amount of time
playing during their first few weeks
(Tileston and Lechleitner 1966, p. 300).
White-tailed prairie dog populations
exhibit large fluctuations of more than
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50 percent from year to year (Menkens
and Anderson 1989, p. 345). Population
fluctuations are likely due to disease
cycles, vegetation quantity and quality,
and drought (Seglund and Schnurr
2009, p. 16) (see Factor A. Climate
Change; Factor C. Disease). We do not
know the level at which population
fluctuations are a natural part of whitetailed prairie dog ecology, or the result
of environmental or human-caused
threat factors. In many cases, prairie dog
colonies persist despite large population
fluctuations (see Factor C. Disease). We
define ‘‘persistence’’ as the long-term
continuance of white-tailed prairie dog
colonies, at a high enough level to exist
in the long-term with minimal
management assistance.
White-tailed prairie dogs are diurnal
(active during the day) (Tileston and
Lechleitner 1966, p. 200). They are
active approximately 5 to 7 months per
year from early spring to fall and
hibernate during late fall and winter
(Clark 1977, pp. 59-60; Cooke 1993, p.
11). Time spent hibernating is
determined by available food resources
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(Clark 1977, p. 60). In warm weather,
even in mid-winter, white-tailed prairie
dogs will feed if grasses are growing
(Hollister 1916, p. 6; Goodrich and
Buskirk 1998, p. 177). If resources are
not sufficient, prairie dogs become
inactive and spend more time in their
burrows (Harlow and Menkens 1986, p.
795). During periods of high summer
temperatures, white-tailed prairie dogs
avoid the highest temperatures of
midday by foraging in the cooler
morning and evening hours (Clark 1977,
p. 58).
Distribution and Abundance
The overall species’ distribution is
mapped as ‘‘gross range.’’ The available
white-tailed prairie dog literature uses
the term ‘‘gross range’’ to describe the
outer boundary identifying the overall
rangewide distribution of the whitetailed prairie dog (Figure 1). However,
not all lands within the species’ gross
range are occupied or have the potential
to be occupied by white-tailed prairie
dogs (Seglund et al. 2006, p. 100). The
predicted range is a subset of the gross
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range and thus represents a more
accurate spatial representation of the
potential range of the white-tailed
prairie dog (Seglund et al. 2006, pp. 16,
110; Seglund and Schnurr 2009, p. 23).
Predicted range is defined using habitat
characteristics of vegetation, land use,
slope, and elevation (Seglund et al.
2006, pp. 14-39). Depending on
available data, we use gross range,
predicted range, or mapped occupied
habitat throughout this document to
evaluate status and threats to the
species. For example, gross range
mapping data was available for our use
for all States across the species’ range.
However, the data for the predicted
range map (Seglund et al. 2006, p. 110;
Seglund and Schnurr 2009, p. 23) was
only available for the State of Colorado.
Information regarding mapped occupied
habitat (all areas mapped on Federal
lands as occupied by white-tailed
prairie dogs since 1985) was available
for the State of Utah, but not for any
other States.
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The white-tailed prairie dog occurs
from a small area in south-central
Montana, throughout much of
Wyoming, into western Colorado, and
northeastern Utah. There are 20,224,801
ha (49,976,572 ac) within the gross
range of the white-tailed prairie dog and
13,066,887 ha (32,288,981 ac) within the
species’ predicted range (Seglund et al.
2006, p. 91). Therefore, approximately
65 percent of the gross range has the
characteristics necessary to support the
white-tailed prairie dog. Wyoming
contains the largest amount of whitetailed prairie dog predicted range (75
percent) (Knowles 2002, p. 4). Less than
1 percent of predicted range occurs in
Montana (Table 1). The majority of
white-tailed prairie dog predicted range
(56 percent) occurs on land managed by
the Bureau of Land Management (BLM).
A significant portion of the predicted
range occurs on private land (37
percent). Very little of the predicted
range is managed by the Service (0.4
percent), U.S. Forest Service (USFS) (0.5
percent), or National Park Service (NPS)
(0.9 percent) (Table 1).
TABLE 1. PERCENT PREDICTED RANGE BY STATE AND LAND MANAGEMENT ENTITY (SEGLUND et al. 2006, PP. 91, 98,
100, 104, 109).
Total Range
Private
BLM
USFS
NPS
USFWS
State
Other
Colorado
11
37
56
<1
1
<1
5
<1
Montana
<*1
49
44
2
0
0
5
<1
Utah
13
20
60
<1
<1
<1
11
7
Wyoming
75
33
54
<1
<1
<1
6
6
37
56
<1
<1
<1
5
<1
Total
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* < less than
Historical abundance and distribution
are not well documented for whitetailed prairie dogs prior to the 1980s
(Pauli et al. 2006, p. 13; Seglund et al.
2006, p. 11). The distribution of whitetailed prairie dogs has not changed
appreciably since historic times
(Knowles 2002, pp. 5-6). The only
recorded change in distribution is in
Montana, where white-tailed prairie
dogs were previously captured 40 miles
north of currently occupied habitat
(Knowles 2002, p. 5). However,
abundance declined as a result of past
control efforts and plague (Cully 1993,
p. 38; Knowles 2002, pp. 1-2) (see
Factor B. Overutilization and Factor C.
Disease). We are not able to quantify
changes in occupied habitat for the
species because mapping did not use
standardized methods, and we do not
have accurate estimates of historical
occupied habitat (Seglund et al. 2006, p.
13).
We do not have rangewide population
trend information due to a lack of
historical population information and
inconsistencies in survey methodologies
(Seglund et al. 2006, pp. 4, 13). Surveys
for white-tailed prairie dog distribution
and occupancy rates were recently
conducted across portions of the
species’ gross range (Grenier and Filipi
2009, entire; Seglund and Schnurr 2009,
p. 27; Wright 2009, entire). While
occupancy surveys are intended to
determine population trends (Seglund
and Schnurr 2009, p. 10), the data are
not yet available to provide trend
information. In addition, each State
used different methods to conduct
ground surveys and determine
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occupancy rates; thus, the results are
not comparable. We present State-byState information below with the caveat
that comparing colony occupancy rates
across the gross range of the species is
not possible.
Colorado
White-tailed prairie dog predicted
range includes Moffat, Routt, Rio
Blanco, Garfield, Mesa, Delta, Montrose,
Eagle, Jackson, Ouray, and Larimer
Counties in northwestern Colorado
(Seglund et al. 2004, p. 133).
Approximately 1,246,441 ha (3,104,733
ac) of predicted white-tailed prairie dog
habitat occurs in three Individual
Population Areas (IPAs): Grand ValleyUncompahgre IPA, North IPA, and
Northwest IPA (Hotze 2010, pp. 9-10).
An IPA is an area physically separated
from other populations that may face a
unique subset of threats (Seglund and
Schnurr 2009, p. 1). These population
areas are geographically separated from
each other but connected to population
areas in Utah and Wyoming (Seglund
and Schnurr 2009, p. E-5).
Colorado completed Statewide whitetailed prairie dog surveys in 2004 and
2008; occupancy rates were 24.1 and
23.1 percent, respectively, a statistically
insignificant difference (Seglund and
Schnurr 2009, pp. 27-28). Occupancy
rate is the number of randomly selected
plots in predicted habitat with prairie
dogs, and is not a measure of
abundance. We do not have population
trend information across the entire
predicted range of the species in
Colorado. Localized declines and
habitat degradation were reported in the
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Grand Valley-Uncompahgre IPA due
largely to urbanization (Seglund and
Schnurr 2009, p. 54). Information in the
North IPA is restricted to colonies
associated with black-footed ferret
reintroduction; a historical record of
ferrets in this area suggests it once
supported abundant populations of
prairie dogs (Seglund and Schnurr 2009,
p. 58). Only two colonies remain,
although they have remained stable for
the past 20 years (Seglund and Schnurr
2009, p. 58). Population densities and
distribution in the Northwest IPA
appear to fluctuate greatly in large part
due to the prevalence of plague
(Seglund and Schnurr 2009, pp. 63-76).
Montana
White-tailed prairie dogs occur in one
population area in Carbon County, along
the Montana-Wyoming border (Seglund
et al. 2006, p. 25). Fifteen colonies were
mapped in the 1970s across 312.8 ha
(773 ac) (Flath 1979, p. 63). White-tailed
prairie dogs were previously reported in
north Sage Creek in Carbon County
(Hollister 1916, p. 27), and in
Yellowstone County just northeast of
Carbon County (Kelso 1939, p. 7), but no
animals were found in these locations in
later surveys (Flath 1979, entire).
Current occupied area of white-tailed
prairie dogs in Montana includes 112 ha
(277 ac) across 11 colonies; 8 colonies
were considered active in 2009 (MFWP
2009a, p. 1). The apparent loss in
occupied habitat is likely due to plague
and agricultural land conversion (Parks
et al. 1999 in Knowles 2002, p. 15). We
do not have population trend data for
the white-tailed prairie dog in Montana.
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Utah
White-tailed prairie dogs occur in
Rich, Summit, Daggett, Uintah,
Duchesne, Carbon, Emery, and Grand
Counties (Seglund et al. 2004, p. 140) in
northern and eastern Utah. In 2002 and
2003, 57,463 ha (141,808 ac) of
occupied white-tailed prairie dog
habitat were documented, mostly within
Uintah and Duchesne Counties (Lupis et
al. 2007, p. 17). Smaller population
areas are found in the Cisco Desert in
Emery and Grand Counties (10,869 ha
(26,856 ac)), and in Rich County (73 ha
(180 ac)) (Lupis et al. 2007, p. 15).
Surveys did not include private lands;
therefore, the amount of occupied
habitat is an underestimate. These
population areas are mostly
disconnected from each other, but
connect to population areas in Wyoming
and Colorado. Based on surveys
conducted in 2008, the white-tailed
prairie dog occupancy rate was 46
percent of sampled plots (Wright 2009,
p. 5).
We do not have information on longterm population status or trends for
white-tailed prairie dogs in Utah.
Surveys in black-footed ferret
management areas in the Uintah basin
recorded fluctuating population levels:
increasing densities since the early
1990s, declines in 1999 and 2003, and
population recoveries in 2004-2008
(Seglund et al. 2006, p. 28; Maxfield
2009, pers. comm.) (see Factor A.
Climate Change).
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Wyoming
White-tailed prairie dogs are found in
the Counties of Big Horn, Park, Hot
Springs, Natrona, Fremont, Sublette,
Sweetwater, Lincoln, Uinta, Carbon, and
Albany in northern and southern central
Wyoming (Seglund et al. 2004, p. 130).
Wyoming Fish and Game documented
11,511,356 ha (27,822,847 ac) of
potential habitat and 1,170,952 ha
(2,893,487 ac) of occupied habitat in
2008 by aerial survey (Grenier and Filipi
2009, p. 5). The majority of these acres
are in Albany and Carbon Counties.
Habitat in Wyoming is mostly
continuous and not split into discrete
population areas. Approximately 68
percent of the surveyed areas were
estimated to be occupied (Grenier and
Filipi 2009, p. 5). This estimate is not
a statistically determined ‘‘occupancy
rate.’’ Occupancy from these aerial
surveys cannot be compared with
ground surveys from Colorado and
Utah, because the observed location of
colony boundaries varies between
methods, presumably due to the
difficulty in measuring colony
boundaries from the air (Andelt et al.
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2005, p. 3). We do not have long-term
status or trend information for whitetailed prairie dogs in Wyoming.
Summary of White-Tailed Prairie Dog
Population Status
We do not have reliable long-term
historical or current white-tailed prairie
dog status, trend, or distribution data.
White-tailed prairie dog populations are
likely below historical levels, though
their overall distribution has not
substantially changed (Knowles 2002, p.
6). Large acreages of occupied habitat
exist across the species’ range,
particularly in Wyoming. Each State
plans to continue occupancy surveying,
so more information may be available in
the future.
Evaluation of Information Pertaining to
the Five Threat Factors
Section 4 of the Act and
implementing regulations (50 CFR 424)
set forth procedures for adding species
to, removing species from, or
reclassifying species on the Federal
Lists of Endangered and Threatened
Wildlife and Plants. Under section
4(a)(1) of the Act, a species may be
determined to be endangered or
threatened based on any of the
following five factors:
(A) The present or threatened
destruction, modification, or
curtailment of its habitat or range;
(B) Overutilization for commercial,
recreational, scientific, or educational
purposes;
(C) Disease or predation;
(D) The inadequacy of existing
regulatory mechanisms; or
(E) Other natural or manmade factors
affecting its continued existence.
In making this 12–month finding,
information pertaining to the whitetailed prairie dog in relation to the five
factors provided in section 4(a)(1) of the
Act is discussed below. In making our
12–month finding on the petition we
considered and evaluated the best
available scientific and commercial
information.
Factor A. The present or threatened
destruction, modification, or
curtailment of the species’ habitat or
range.
The following potential factors that
may affect the habitat or range of the
white-tailed prairie dog are discussed in
this section, including: (1) Oil and gas
exploration and development, (2) oil
shale and tar sands development, (3)
mineral development, (4) renewable
energy development—wind and solar,
(5) urbanization, (6) agricultural land
conversion, (7) grazing, (8) fire
occurrence and suppression, (9)
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invasive plant species and (10) climate
change.
Oil and Gas Exploration and
Development
Exploration and development of oil
and gas resources is widespread
throughout the gross range of the whitetailed prairie dog (Hotze 2010, pp. 1126). Between 2004 and 2008,
exploration of oil and gas in the
intermountain west increased
substantially because of political and
economic incentives (National
Petroleum Council 2007, pp. 5-7). The
2005 Energy Policy Act expedited the
leasing and permitting process on
Federal lands (42 U.S.C. 15801). The
global recession of 2008 resulted in
decreased energy demand resulting in a
reduced rate of energy development.
Fossil fuel production is expected to
regain and surpass the early 2008 levels
in 2010-2030 (Copeland et al. 2009, p.
1; Energy Information Administration
(EIA) 2009, p. 109).
Energy development includes
exploration, drilling, production, and
reclamation phases (Tribal Energy and
Environmental Information
Clearinghouse (TEEIC) 2009, entire),
each of which may potentially impact
the white-tailed prairie dog or its
habitat. During the exploration phase,
oil and gas resources are delineated
using a variety of technologies,
including seismic shot-hole surveys
(planting and detonation of
underground explosives to produce
vibrations that reveal locations of
mineral resources) and vibroseis trucks
(vehicle with a vibration plate used to
survey mineral resources) (TEEIC 2009,
p. 6). These activities may result in
mortality and the crushing of vegetation
along the seismic route, but there are no
permanent structures established during
the exploration phase. If oil and gas
resources are proven, the lessee moves
into the drilling phase. During the
drilling phase, access roads and well
pads are constructed, pipelines are
installed, and the infrastructure
necessary for the production phase
(such as compressor stations) is
developed and constructed (TEEIC
2009, p. 9). This phase typically results
in longer-term disturbance to whitetailed prairie dog habitat. The
production phase includes maintaining
the wells and infrastructure as well as
continuing the extraction of the oil and
gas resources. Wells may be in the
production phase for up to 20 to 30
years for gas wells (TEEIC 2009, p. 5)
and up to 100 years for oil wells
(Connelly et al. 2004, p. 7:41). The final
phase begins when a well is no longer
producing oil or gas because the
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resource is depleted. The lessee is
responsible for reclaiming the land back
to its original condition, or as close to
the original condition as possible (BLM
2007a, p. 2; TEEIC 2009, p. 15).
Oil and gas developments are
typically configured as point (e.g., well
pads, compressors) and line (e.g., roads,
pipelines) disturbances across broad
areas. The amount of direct habitat loss
may encompass 5 to 10 percent of
leased areas. However, the extent of
disturbance to white-tailed prairie dogs
may reach far beyond the direct habitat
loss, due to the loss and fragmentation
of habitats; the alteration of vegetation
resources, which often promotes
nonnative invasive plant species;
increased noise levels; increased vehicle
traffic; and increased human access to
previously remote areas (Pauli et al.
2006, p. 27; Seglund et al. 2006, p. 46;
Seglund and Schnurr 2009, p. 126;
Wyoming Game and Fish Department
(WGFD) 2009, p. 10). The amount of
direct habitat loss and total
fragmentation varies greatly depending
on well density (number of acres per
well) and spacing (distance between
individual well pads). Increasing wells
per unit area decreases the amount of
habitat available for wildlife. Well
densities and spacing are typically
designed to maximize recovery of the
resource and are administered by State
oil and gas agencies and the BLM on
Federal mineral estate. Each geologic
basin has a standard spacing, but
exemptions are granted (Connelly et al.
2004, pp. 7-39 to 7-40). Within the range
of the white-tailed prairie dog, well
spacing can vary from 5 to 160 acres per
well. Larger well spacing is often
characterized by more wells drilled per
pad. Increasing the number of wells per
pad increases the size of the individual
pad but decreases the amount of habitat
fragmented. The variation in well and
well pad spacing results in a variation
in the intensity of effects across the
species’ range. However, we are unable
to determine how the ultimate effects to
the species vary with well density. The
threshold levels of oil and gas
development that result in reduced
populations or eliminated colonies are
unknown.
Resulting impacts to white-tailed
prairie dogs from oil and gas
development may include direct
mortality from vehicles; direct mortality
associated with increased access by
recreational shooters who utilize the
new access routes (Gordon et al. 2003,
p. 12); increased disturbance responses
from increased human activity; direct
loss of habitat and forage resources
during exploration, drilling, and
production; and indirect loss of forage
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resources from invasive, nonnative
plant species (Seglund and Schnurr
2009, p. 126).
No studies have been done regarding
the short-term or long-term impact of oil
and gas development on individual
white-tailed prairie dogs or their
colonies. White-tailed prairie dogs can
be negatively impacted by the direct
loss of habitat that occurs as a result of
development. For example, white-tailed
prairie dog burrow densities were lower
at well locations compared to areas
further from the well pads (Biggins et al.
1984, p. 12). Dead prairie dogs were
found in oil and gas reserve pits (Esmoil
1995 in Peterson 2008, p. 5), although
the extent of population level impact is
not known. The use of vibroseis trucks
in prairie dog colonies appears to
impact vegetation, but preliminary
results did not document prairie dog
mortality or burrow collapse (Young
and Sawyer 1981, pp. 1-2; Menkens and
Anderson 1985, p. 7).
However, as described above,
exposure to a factor does not necessarily
indicate that the factor is a threat. We
know that white-tailed prairie dog
colonies exist in areas with long-term
oil and gas development. Some of the
largest and most robust colonies are
located near areas of intense oil and gas
development (see Distribition and
Abundance, above, and our discussion
under Factor C, below). For example,
the Coyote Basin, Kennedy Wash, and
Snake John colonies in Uintah County,
Utah, occur within a landscape
fragmented by oil and gas infrastructure,
although their immediate occupied
habitats have not sustained significant
energy development. Fifty percent of the
mapped occupied habitat in this region
has been leased with 17 percent
currently producing (See Utah, below).
Populations in this area have fluctuated;
although this has been attributed to
drought (See Climate Change, below).
Despite the high amount of leasing in
this area, populations have recovered to
their 20 year recorded peak. Similarly,
Coyote Basin and Wolf Creek are
historically Colorado’s most robust
colonies and occur within the
Northwest IPA where oil and gas
development is high. Forty one percent
of this IPA has already been leased, with
7 percent currently producing (Hotze
2010, p. 20). Prairie dogs continue to
occupy a moderately sized complex
within the Coal Oil Basin (Colorado’s
largest oil field) despite an active
drilling history that extends back to
1944 (Wolf Creek Work Group 2001, p.
15).
Available information does not
indicate that white-tailed prairie dogs
are currently reacting to oil and gas
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activities on a local landscape scale or
at the population or species level. We
also do not know if there is a level of
oil and gas development at which the
status of prairie dogs at the population
or species level would be negatively
impacted. As described above, whitetailed prairie dogs persist in several
areas with oil and gas activity.
To evaluate the extent to which oil
and gas development may affect whitetailed prairie dogs in the foreseeable
future, we overlaid BLM-authorized oil
and gas leases with the species’ gross
range. More specific information was
available for Utah and Colorado, so we
overlaid oil and gas development with
white-tailed prairie dog predicted range
(Seglund and Schnurr 2009, p. 24) in
Colorado and mapped occupied habitat
in Utah (Hotze 2010, p. 7). We also
reviewed information on State-specific
potential oil and gas reserves where that
information was available. The results
are presented below and in the State-byState analysis sections.
In additional to managing lands in
Wyoming, Colorado, and Utah, the BLM
manages the Federal mineral estate,
including authorizing oil and gas leases.
Leases may be producing or nonproducing. Producing leases are those
being actively developed. Nonproducing leases are leased; however,
the resources for which they were
leased are not currently being extracted.
Non-producing leases may become
developed in the future, but
development is not guaranteed
(Thompson 2010, pers. comm.). We
consider these leases to be indicative of
potential development. However, we do
not know the percent of non-producing
leases that will become developed in the
future because the variables governing
development are complex and include
the price of gas, the number of other
leases the company holds, the actual
amount of resource the lease contains
(often unknown at the time of lease),
and other complex economic and social
factors.
In addition to the producing and nonproducing leases, BLM has authorized a
significant amount of the Federal
mineral estate that may be leased in the
future. Each BLM field office developed
a resource management plan that
delineates areas available for leasing
and depicts surface access constraints
(e.g., BLM 2008a, p. 7). The areas that
are available for leasing are larger than
those that have already been authorized,
and include areas that may be
developed in the future should proven
reserves be located. Development of the
entire area available for leasing is
unlikely due to BLM’s multi-use
mandate, but the area available for
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leasing represents a potential maximum
of oil and gas development. Non-Federal
mineral estates are managed by State,
tribal, and private mineral rights owners
under different programs and using
different processes.
We were unable to specifically
quantify the impacts of development on
non-Federal mineral rights. Total active
and plugged wells are available as GIS
layers from each State’s oil and gas
development commission. However,
number of wells is not a biologically
meaningful measure to the white-tailed
prairie dog because the effects depend
on the amount of land leased and well
density and spacing. As previously
stated, the impacts to the species at
different well spacing densities are not
well understood. Approximately twothirds of wells within the species range
are located on Federal versus nonFederal estate (BLM 2009; Colorado Oil
and Gas Conservation Commission
2010; Wyoming Oil and Gas
Conservation Commission 2010; Utah
Division of Oil and Mining 2010;
unpublished data). Similarly,
approximately two-thirds of the species
range is in Federal vs. non-Federal
ownership. We assume that a similar
ratio of development of non-Federal
minerals is likely to occur in the future
as is occurring for Federal minerals.
Because leasing does not guarantee
development, and the fact that we are
unable to estimate leasing rates on nonFederal estate, we consider the numbers
presented below (in the State-by-State
analysis) as an approximate
measurement of Federal and nonFederal development that could occur
in the foreseeable future.
The BLM has authorized 5,687,259 ha
(14,053,523 ac) of producing and nonproducing leases for oil and gas
development, representing
approximately 28 percent of the whitetailed prairie dog’s gross range (Hotze
2010, p. 18). Producing leases occur
across 1,435,580 ha (3,547,395 ac), or 7
percent, of the species’ gross range
(Hotze 2010, p. 18). Future exploration
and development of fossil fuels is likely
to focus in areas of highest potential
return. Highest potential return is
defined by several geological
characteristics including permeability
and porosity of the underlying rock
(BLM 2005a, p. 41). For example, in the
BLM Little Snake field office of
northwest Colorado, approximately 96
percent of new wells will be drilled in
areas with high oil and gas potential
(BLM 2007b, p. 3:100). In high and
moderate potential areas in Wyoming, a
single well can produce 4 to 30 times as
much as a well in low potential areas
(BLM 2008b, p. A20:6). Therefore, we
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assume these areas will be the focus of
future leasing.
Colorado
In Colorado, the BLM authorized oil
and gas leases on 30 percent of the
white-tailed prairie dog’s predicted
range in the State (Hotze 2010, p. 20)
across the Northwest, North, and Grand
Valley-Uncompahgre IPAs. Of the
authorized oil and gas leases within the
predicted range in Colorado, there are
61,334 ha (151,560 ac) of producing
leases, which comprise approximately 5
percent of the predicted State range
(Hotze 2010, p. 14). Non-producing
leases encompass 311,650 ha (770,104
ac), or approximately 25 percent of the
predicted State range (Hotze 2010, p.
14).
Northwest Individual Population Area
(IPA)
The Northwest IPA in Moffat and Rio
Blanco Counties is within the Greater
Green River Basin (DOI et al. 2006, p.
20) and has the highest potential for oil
and gas development (Seglund and
Schnurr 2009, p. 61). This IPA
comprises approximately 54 percent of
white-tailed prairie dog predicted
habitat in Colorado (Hotze 2010, p. 10).
Authorized lease areas in 2009
encompassed approximately 41 percent
of the Northwest IPA (Hotze 2010, p.
20), and oil and gas development is
projected to significantly increase over
the next 20 years (Seglund and Schnurr
2009, p. 128). For example, the BLM
anticipates authorizing the drilling of
3,031 oil and gas wells over the next 20
years in Routt and southwestern Moffat
Counties (BLM 2007b, p. 3:100),
whereas the previous 20 years resulted
in 594 drilled wells (BLM 2007b, p.
3:99). Similarly, the BLM anticipates
between 17,800 and 21,200 new wells
will be drilled over the next 20 years in
Rio Blanco and central and northern
Moffat Counties, whereas there were
5,800 wells drilled previously (Seglund
and Schnurr 2009, p. 129). However, the
majority of these wells will occur
outside of the white-tailed prairie dog’s
predicted range (Seglund and Schnurr
2009, p. 129). Approximately 96 percent
of new wells will be drilled in areas
with high oil and gas potential as
defined by the BLM (2007b, p. 3:100);
we believe this localizes the
development to some extent and thus
limits the amount of prairie dog habitat
impacted.
Three potential coal bed methane
areas partially overlap white-tailed
prairie dog habitat in the Northwest
IPA: eastern Sand Wash Basin, Lower
White River, and Danforth Hill (BLM
2007b, p. 3:102). However, the majority
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of the coal bed methane areas occur
outside the predicted range for the
species within Colorado (BLM 2007b,
Figure 3-16; Seglund and Schnurr 2009,
p. 119).
Grand Valley-Uncompahgre IPA
There is potential for energy
development to occur in a corridor of
the Grand Valley-Uncompahgre IPA in
Mesa, Montrose, and Ouray Counties
(Seglund and Schnurr 2009, p. 54).
Approximately 14 percent of the whitetailed prairie dog’s predicted range in
this IPA is authorized for lease or
contains pending leases from the BLM
(Seglund and Schnurr 2009, p. 131;
Hotze 2010, p. 20). The BLM estimates
authorizing 3,600 wells on 1,519 pads
over the next 20 years in this IPA
(Ewing 2009, pers. comm.). The total
area disturbed is estimated at 13,200 ac
(5,342 ha) of short-term disturbance and
4,100 ac (1,659 ha) of long-term
disturbance (Ewing 2009, pers. comm.).
We do not know where this
development will occur with respect to
known prairie dog colonies. However,
85 percent of this IPA remains unleased,
and future wells represent a relatively
small (less than 2 percent of this IPA)
amount of additional disturbance.
North IPA
Crude oil was historically produced
in the North IPA to a limited degree.
However, EOG Resources discovered a
large reservoir of crude oil in this area
in 2008, and subsequently acquired a
lease for 100,000 ac (40,469 ha) of land
in the area (Seglund and Schnurr 2009,
p. 129). Approximately 25 percent of the
white-tailed prairie dog’s predicted
range in the North IPA has authorized
or pending leases (Seglund and Schnurr
2009, p. 131; Hotze 2010, p. 20).
In summary, BLM has authorized and
has pending leases on approximately 30
percent of the predicted range of the
species within Colorado for oil and gas
development (Seglund and Schnurr
2009, p. 131; Hotze 2010, p. 20). The
largest potential for overlap and impacts
to white-tailed prairie dogs occurs in the
Northwest IPA; oil and gas development
is projected to increase substantially in
this IPA over the next 20 years (Seglund
and Schnurr 2009, p. 129). We expect
the majority of future oil and gas
development to occur in this IPA. We
do not know the exact locations of
energy development facilities with
respect to locations of white-tailed
prairie dog colonies. Oil and gas
development will likely impact whitetailed prairie dogs, causing individual
mortalities and habitat loss and
fragmentation. However, the majority of
oil and gas development will occur in
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areas of high potential energy reserves,
and particularly in the Northwest IPA,
so impacts to the species are likely to be
more localized, and are not expected to
occur at high levels across the species’
predicted range in Colorado. Based on
the available information, we do not
believe oil and gas development in
Colorado is a threat to the species now
or in the foreseeable future.
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Montana
White-tailed prairie dog habitat in
Montana represents less than 1 percent
of the gross range of the species
(Seglund et al. 2006, p. 91), and is
contained entirely within Carbon
County. Therefore we did not calculate
the area impacted by oil and gas leasing.
The area containing the South Sage
Creek white-tailed prairie dog colony
was leased in January 2002, but is not
yet developed (Begley 2010a, pers.
comm.). The South Sage Creek colony
occupies less than 6 ha (15 ac), or 5
percent of the occupied habitat in
Montana (MFWP 2009b, p. 3). The area
containing the Robertson Draw colony is
available for leasing but has not yet been
leased (Begley 2010a, pers. comm.). Oil
and gas development is not impacting
the remaining six colonies in Montana
(Seglund et al. 2006, p. 26). Because of
the small amount of habitat impacted,
oil and gas development is not a
significant threat in this State, now or in
the foreseeable future.
Utah
The BLM has authorized oil and gas
leases on 31 percent of the white-tailed
prairie dog’s gross range in Utah (Hotze
2010, p. 18). The highest overlap
between the gross range of the whitetailed prairie dog and oil and gas
development potential occurs in Uintah,
Duchesne, Grand, and Carbon Counties
(Hotze 2010, pp. 21-22; Utah
Department of Natural Resources 2004
in Seglund et al. 2006, p. 33).
The Uinta and Piceance Basin areas of
Utah have significant oil and gas
resources (BLM 2008a, p. 3:38).
Approximately 82 percent of 18,982
existing well locations in Utah occur in
the Uinta Basin in Duchesne and Uintah
Counties (Hotze 2010, pp. 15-16). There
are 97,266 ha (240,350 ac) of mapped
occupied white-tailed prairie dog
habitat in Uinta and Duchesne Counties
(Hotze 2010, pp. 7-8). The BLM has
authorized oil and gas leasing on
approximately 51 percent of this
mapped occupied habitat (Hotze 2010,
p. 22). The BLM estimates that
approximately 2,055 new oil wells,
4,345 new gas wells, and 130 new coal
bed methane wells will be drilled
within the Uinta Basin during the 15- to
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20–year planning period (BLM 2008a, p.
3:36). Approximately 73 percent of the
Federal mineral rights open to leasing in
the Uinta Basin area have already been
authorized (Hotze 2010, p. 24).
Therefore, the authorized leases
represent a fair assessment of the
potential impact to white-tailed prairie
dogs. These leases have a 201-meter
(660-ft) no surface occupancy
stipulation adjacent to occupied prairie
dog colonies, which will minimize
direct mortality of prairie dogs and the
loss of habitat from future development
(see Factor D. Inadequacy of Regulatory
Mechanisms, below, for a discussion of
these stipulations).
There are 14627 ha (36,144 ac) of
mapped white-tailed prairie dog habitat
in Carbon and Emery Counties (Hotze
2010, p. 8). The BLM has authorized oil
and gas leasing on approximately 52
percent of this occupied mapped habitat
(Hotze 2010, p. 22). About 2300 ha
(5,600 ac) (15 percent) of this habitat is
located within areas considered to have
high potential for oil and gas resources
(BLM 2004, p. 4:119). These leases also
have a no surface occupancy stipulation
for prairie dog colonies (see Factor D).
In summary, oil and gas leasing and
development is authorized by BLM
across 31 percent of the species’ gross
range in Utah. The majority of current
and future project development occurs
in the Uinta Basin in northeastern Utah,
and thus potential impacts to the
species could be greatest in this area,
particularly because 52 percent of the
species’ mapped occupied habitat is
leased. We consider the Uinta Basin to
be the highest potential development
area in Utah. Exploration and drilling,
as previously discussed, can result in
mortality of individual prairie dogs and
the loss and fragmentation of habitats.
However, robust white-tailed prairie dog
colonies continue to persist in the Uinta
Basin, in areas associated with existing
oil and gas development. The BLM
imposes a no surface occupancy
stipulation that prohibits activity within
201 meters (660 ft) of white-tailed
prairie dog colonies in the Uinta Basin
(see Factor D), which will minimize
direct mortality of prairie dogs and the
loss of habitat from future development.
The likely concentration of oil and gas
development in high potential resource
areas should also minimize the amount
of white-tailed prairie dog habitat
directly lost to development. Due to
these factors, we do not believe oil and
gas development in Utah is a threat to
the species now or in the foreseeable
future.
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Wyoming
Seventy-seven percent of the species’
gross range in Wyoming overlaps
potential energy resources in Wyoming
(Seglund et al. 2006, p. 39). However,
not all potential energy resources will
be developed. Therefore, we further
reviewed leases and potential energy
resources to determine the extent of
development in the foreseeable future
(the next 20 years).
Approximately 3,443,269 ha
(88,508,503 ac) of land, or 27 percent of
the species’ gross range in Wyoming, is
authorized for leasing by BLM (Hotze
2010, p. 18). These leases are either
producing or are non-producing.
However, we expect the majority of new
wells will be drilled in areas with high
oil and gas potential. In high and
moderate potential areas in Wyoming, a
single well can produce 4 to 30 times as
much as a well in low potential areas
(BLM 2008b, p. A20:6). Most wells will
be drilled in areas of high potential oil
and gas resources (Copeland et al. 2009).
Only 415,649 ha (1,027,057 ac), or 4.2
percent of the species’ predicted range
in Wyoming, occurs in high potential oil
and gas resource in areas as defined by
Seglund et al. (2006, p. 39). Low and
medium potential oil and gas resources
overlap 73 percent of the gross range of
white-tailed prairie dog (Seglund et al.
2006, p. 39). Twenty-three percent of
the gross range has no oil or gas
resources. Given the existing
development, we consider the area in
southern Wyoming between Rawlins
and Rock Springs to be a high potential
area (Hotze 2010, p. 11).
Oil and gas development and reserves
occur throughout the gross range in
Wyoming. We do not know the exact
locations of future energy development
facilities with respect to locations of
white-tailed prairie dog colonies. Oil
and gas development will likely impact
white-tailed prairie dogs, causing
individual mortalities and habitat loss
and fragmentation. However, as
previously discussed, only a small
portion (4.2 percent) of the species’
gross range overlaps areas of high
potential energy reserves. Energy
development is most likely to be
concentrated in areas of high potential
reserves, so impacts to the white-tailed
prairie dog will not occur at high levels
across the species’ entire gross range in
Wyoming. Based on the available
information, we do not believe oil and
gas development in Wyoming is a threat
to the species now or in the foreseeable
future.
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Summary of Oil and Gas Development
Table 2 (below) gives a summary of
the percentage of BLM-leased area for
oil and gas in gross, predicted, and
mapped occupied range, by State.
Generally, the area attributed to
producing leases makes up a small
30347
portion of the species’ range, although
up to 28 percent of the species’ gross
range has been leased for potential
development.
TABLE 2. PERCENTAGE OF LEASED AREA FOR OIL AND GAS IN GROSS, PREDICTED, AND MAPPED OCCUPIED RANGE OF THE
WHITE-TAILED PRAIRIE DOG.
(Totals include a small amount of land authorized for leasing but not yet leased; and therefore not included in the other two categories.)
Percent
Producing
Leases
Percent
NonProducing
Leases
Total
Percent
Leased*
9
20
30
Northwest IPA (Predicted)
7
34
41
North IPA (Predicted)
2
22
25
Grand Valley/Uncompahgre IPA (Predicted)
3
11
14
Total, Predicted range
5
25
30
10
19
31
Uintah Basin (mapped occupied)
17
32
51
Carbon and Emery Counties (mapped occupied)
4
48
52
Wyoming (Gross)
6
21
27
Total (Gross)
7
20
28
State
Colorado (Gross)
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Utah (Gross)
Oil and gas development is a major
cause of development in the gross range
of the species and is likely to continue
into the foreseeable future at similar
rates of development. Twenty-eight
percent of the species’ gross range is
authorized for leasing. Leasing does not
guarantee development, and therefore
we consider the area leased Federally to
be an estimate of the rangewide
development, including non-Federal
estate. A minimum of 13,000 additional
wells will be authorized in the
foreseeable future. However, energy
development will not occur uniformly
across the landscape. Most development
will occur in areas of high resource
potential. Development is also mediated
by variations in well density and
spacing. There are localized regions
across the white-tailed prairie dog’s
gross range where development is most
prevalent, including the Uinta Basin in
Utah, the Northwest IPA in
northwestern Colorado, and the
southwestern region of Wyoming. The
impacts to white-tailed prairie dogs
would thus be greater in these locations
than in other parts of the species’ gross
range.
In areas where energy development
overlaps occupied white-tailed prairie
dog habitats, the resulting habitat loss
and fragmentation likely has negative
effects on individuals and populations,
including mortality, noise disturbance,
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and habitat loss and fragmentation.
Presumably, there is a threshold level
wherein habitat loss and fragmentation
may threaten the white-tailed prairie
dog, at least in localized regions.
However, our available information
indicates energy development does not
currently significantly threaten the
species; for example, large prairie dog
complexes continue to persist in areas
of high energy development (see
Colorado and Utah, above). Based on
the information available to us, we have
determined that oil and gas
development does not significantly
threaten the white-tailed prairie dog
now or in the foreseeable future.
Development of Oil Shale, Tar Sands,
and Other Minerals
Extraction of oil shale and tar sands
results in the removal of wide swaths of
habitat. Oil shale and tar sands
development results in a loss of habitat
of the entire lease, although only
portions of the lease would be impacted
at a given time. Impact footprints for oil
shale leases for strip mines are
approximately 2,331 ha (5,760 ac) in
size (BLM 2008c, p. 4:4), and each
surface retort mine (an underground
mine with processing of the material
above ground) is approximately 668 ha
(1,650 ac) (BLM 2008c, p. 4:8). When an
area is processed, the impact footprint
shifts to another portion of the lease,
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and mined areas are reclaimed. The
success of reclamation varies dependent
on site conditions (BLM 2008c, p. 4:71).
Oil shale and tar sand development
activities can result in long- term or
permanent habitat loss and
fragmentation of white-tailed prairie dog
habitats (BLM 2008c, p. 4:109)
depending on the quality and success of
habitat reclamation.
Oil shale and tar sands resources
occur across 8 percent of the gross range
of the species (Hotze, 2010, p. 34).
Approximately 1,228,100 ha (3,034,696
ac) of potentially productive land for oil
shale and tar sands occurs in Wyoming
and Utah (BLM 2008c, p. 2:113), and the
BLM made available 660,215 ha
(1,631,424 ac) of Federal land for leasing
in this area (BLM 2008c, p. ES:7). A very
small portion of the white-tailed prairie
dog’s gross range is identified for leasing
in Colorado (Seglund and Schnurr 2009,
p. 121).
Oil shale and tar sands development
has failed to materialize due largely to
technological problems and unfavorable
economics. Significant economic
questions remain regarding the
development of the Green River
formation oil shale and tar sands
resources (Bartis et al. 2005, pp. 15, 53;
BLM 2006, pp. 7, 15-19, 31, 34-36). The
cost associated with an essentially new
industry using new and innovative
technologies is likely to be great.
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Economic success of oil shale- and tar
sands-derived petroleum will depend
on continuing high and stable
petroleum prices. Due to past
fluctuation of petroleum prices, private
industry has exhibited a reluctance to
proceed with research, development,
and subsequent commercial production
of oil shale. This situation will likely
continue unless the petroleum industry
is convinced that petroleum prices will
remain high well into the future (Bartis
et al. 2005, pp. 59-61; Bunger et al.
2004, pp. 7-9).
Oil shale and tar sands extraction and
development remains a speculative
industry. At this time, we believe it is
unlikely that the BLM will begin leasing
the identified properties for
development within the foreseeable
future, which we define as
approximately 10-15 years. In addition,
while oil shale and tar sands resources
overlap 8 percent of the species’ gross
range, actual oil shale and tar sands
development facilities overlap with only
a small portion (less than 0.1 percent) of
the species’ gross range. We do not
believe development of oil shale and tar
sands is a significant threat to the
species now or in the foreseeable future.
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Mineral Development
Coal, uranium, sand, and gravel
mining can result in the removal of
habitat (BLM 2004, p. 4:12). These
activities have the potential to result in
long-term or permanent habitat loss and
fragmentation, depending on the quality
and success of habitat reclamation.
These activities are not common land
uses on BLM holdings in the gross range
of the species. The BLM solid mineral
leases total 108,170 ha (445,209 ac), less
than 1 percent of the species’ gross
range (Hotze 2010, p. 30). The BLM coal
leases total 88,167 ha (217,866 ac), also
less than 1 percent of the species’ gross
range (Hotze 2010, p. 32). Available
evidence does not suggest solid mineral
leases are more common on private
lands. Available information does not
suggest they will become more
widespread within the species’ gross
range in the future. Given the small
percentage of the gross range impacted
by these activities, we do not believe
mineral development is a significant
threat to the species now or in the
foreseeable future.
Renewable Energy Development—Wind
and Solar
The BLM has accessed areas of
renewable resource potential with the
objective of allowing the industries to
focus development in the areas of
highest potential (BLM and DOE 2003,
p. 2). The majority of the species’ gross
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range (Federal and non-Federal lands)
has a low (~ 5kWh/m2/day) amount of
direct solar resources (BLM and DOE
2003, p. A2). Currently, less than 1
percent of the species’ range has been
leased by BLM for development of solar
resources (BLM 2009, unpublished
data). We are unaware of solar
developments on private land within
the gross range of the species. The
majority of the land containing the
species’ range is federally owned, and
therefore we consider potential solar
developments on non-Federal land to be
insufficient to threaten the species.
Given the limited solar resources and
lack of development to date in the
species’ range, we do not consider solar
energy to be a significant threat to the
species now or in the foreseeable future.
Wind energy could impact the species
by creating habitat loss, disturbance, or
fragmentation; increasing the amount of
invasive vegetation; increasing direct
mortality; and increasing disturbance
from noise and human presence (BLM
2005b, p. 5:42). Wind power has
experienced a rate of expansion greater
than any other renewable energy
resource, and continued increases are
predicted through 2030 (EIA 2009, pp.
47, 74). Depending on costs, wind
power production could increase
nationwide by as much as 38 percent by
2030 (EIA 2009, p. 74).
The BLM manages more land areas of
high wind resource potential than any
other land management agency. In 2005,
the BLM completed the Wind Energy
Final Programmatic Environmental
Impact Statement (EIS) that provides an
overarching guidance for wind project
development on BLM-administered
lands (BLM 2005b, entire). Best
management practices are prescribed to
minimize impacts of all phases of
construction and operation of a wind
production facility. We do not have
information on how or where the EIS
guidance was applied since 2005 and,
therefore, cannot evaluate its
effectiveness.
Wind energy developments leased by
the BLM total 823,358 ha (2,034,562 ac),
or approximately 4 percent of the
species’ gross range (Hotze 2010, p. 28).
Only 5 to 10 percent of a development
will have long-term surface disturbances
(i.e., roads, foundations, substation,
fencing) (BLM 2005b, p. 5:2).
To evaluate the potential of future
wind energy developments to impact
the species, we examined the potential
locations for development. Within the
species’ gross range in Colorado and
Utah, only poor and marginal wind
power resources exist (NREL 2003,
entire; NREL 2004, entire). In Wyoming,
there are pockets of good, excellent, and
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outstanding wind power within the
species’ gross range in Fremont,
Natrona, and Carbon Counties (NREL
2002, entire). The majority (more than
75 percent) of these counties are
federally owned land. However, better
wind power resources (rated as
outstanding and superb, based on wind
speeds) are available east of the species’
gross range (NREL 2002, entire). We
expect areas with the best wind
resources will be developed first and
receive more total development.
We are unable to quantify the wind
development scenario for private lands
in the species’ gross range. No central
organization currently tracks wind
development on private lands. Given
the small amount of private land that
coincides with an economically
developable wind resource, we assume
a maximum development of less than 10
percent of the species’ gross range in
Wyoming.
The BLM maximum potential
development scenario for wind energy
in the entire State of Wyoming is an
estimated total of 3,197,937 ha
(7,902,000 ac) of potentially developable
lands, but a much smaller amount is
likely to be developed on BLMadministered lands (1,497 ha (3,700 ac))
(BLM 2005b, p. 5:2). The BLM estimates
that only 5 to 10 percent of BLM area,
or 150 ha (370 ac) of lands, will have
long-term surface disturbance (BLM
2005b, p. 5:2). We expect that much of
the economically developable land
exists outside the species’ gross range,
and given the small size of the total area
on Federal lands likely to be developed
in Wyoming (1,497 ha (3,700 ac)), and
that the majority of the species’ range
occurs on Federal lands, we do not
expect wind energy development to
have a significant impact on the species.
Because only small portions of the
species’ gross range are currently
impacted by wind development and
expected to be impacted in the future,
we do not believe wind energy
development represents a significant
threat to the species. Given that
projected development is small in
regard to the size of the species’ gross
range, and that the majority of
development will take place where
better resources exist, we expect the
overall impact of wind development on
the white-tailed prairie dog to be low.
Urbanization
Conversion of land for urban
development results in a permanent loss
of habitat and fragmentation for many
species, including the white-tailed
prairie dog. Increases in major
population centers result in increased
infrastructure, such as roads and
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transmission lines. These infrastructure
features may impact habitats beyond the
immediate urban area. Increased
urbanization can introduce domestic
animals, such as dogs and cats, that may
prey on some prairie dogs (Magle and
Crooks 2009, p. 198). Human population
growth may result in an increased use
of surrounding public lands for
recreation (Seglund and Schnurr 2009,
p. 54).
The effects of urban fragmentation on
the white-tailed prairie dog have not
been studied. Some information exists
for the black-tailed prairie dog. Weights
and sex ratios of black-tailed prairie
dogs in urban environments were
within normal ranges for the species
(Magle 2008, p. 116). However, blacktailed prairie dogs were more likely to
occur on larger, contiguous habitats
within the urban environments rather
than smaller, highly fragmented parcels
(Magle and Crooks 2009, p. 197).
Collapses of existing colonies were
observed within highly fragmented
urban environments (Magle and Crooks
2009, pp. 197, 199). This information
suggests that some prairie dogs can
survive in fragmented habitat, but
population loss increases with degree of
fragmentation and amount of time since
fragmentation occurred (Magle and
Crooks 2009, p. 200).
The rate of urbanization within the
Rocky Mountain region is below the
national average (White et al. 2009, pp.
41-42). As of 2004, urbanization affected
0.2 percent of the white-tailed prairie
dog’s gross range (Seglund et al. 2006,
p. 45). Much of the existing and future
predicted urbanization is localized to
specific population centers, as further
described below.
Colorado
Twenty-eight percent of the overall
white-tailed prairie dog’s predicted
range is expected to be impacted by
high density urban development (i.e.,
less than 16 ha (40 ac) per housing unit),
5 percent by moderate density urban
development (16 to 32 ha (40 to 80 ac)
per housing unit), and 8 percent by low
density urban development (greater than
32 ha (80 ac) per housing unit) by 2020
in Colorado (Seglund and Schnurr 2009,
p. 171). Public land comprises 59
percent of the species’ predicted range
in Colorado and is not expected to be
impacted by urbanization (Seglund and
Schnurr 2009, p. 171). We expect that
only moderate and high density urban
development will negatively impact the
species, because low density
developments still provide large
expanses of area for colonies to exist
and allow for connectivity between
colonies.
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The majority of urban development is
predicted to occur in the Grand ValleyUncompahgre IPA (Seglund and
Schnurr 2009, pp. 52, 54). Urbanization
has already fragmented white-tailed
prairie dog habitats in this IPA (Seglund
and Schnurr 2009, p. 54). By 2020, 37
percent of the IPA is expected to be
impacted by high or moderate density
urban development (Seglund and
Schnurr 2009, p. 174). However,
urbanization will be localized largely to
the Grand Junction and Montrose urban
areas. High or moderate density urban
development will occur across much
less of the North IPA (0.9 percent) and
Northwest IPA (0.4 percent) (Seglund
and Schnurr 2009, p. 174).
Urbanization has the potential to
impact the species in Colorado,
particularly in portions of the Grand
Valley/Uncompahgre IPA. However, as
noted above, high-density urbanization
will be localized primarily to the human
population centers of Grand Junction
and Montrose. Because of its localized
impact and the availability of large
acreages of Federal, non-urbanized
lands in the species’ predicted range, we
do not consider urbanization to be a
significant threat to the species in
Colorado now or in the foreseeable
future.
Montana
In Montana, 49 percent of the species’
predicted range is privately owned
(Table 1, above). Private land uses
include grazing, agriculture, and
housing; a metropolitan area is located
in nearby Carbon County. At one time,
31 distinct white-tailed prairie dog
colonies occurred in Montana.
Urbanization resulted in the loss of 3
colonies to road construction and
development (Begley 2010b, pers.
comm.). An additional 20 colonies were
lost to impacts associated with mining,
agriculture, or other unknown causes
not directly attributable to urban
development (Begley 2010b, pers.
comm.).
Of the eight remaining colonies in
Montana, four occur on privately owned
land (Begley 2010b, pers. comm.). Three
of these colonies are in areas that
support livestock grazing (Begley 2010b,
pers. comm.). We are unaware of any
plans to develop these properties in the
foreseeable future. The remaining four
colonies occur on Federal lands and are
thus not threatened by urbanization.
Therefore, we do not consider
urbanization in Montana to significantly
threaten the species now or in the
foreseeable future.
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30349
Utah
Urban development is expected to
expand by 188,600 ha (466,041 ac)
across the State of Utah by the year 2030
(White et al. 2009, p. 44). However,
development is localized to
metropolitan areas along the Wasatch
front in Weber, Morgan, Summit, Davis,
Salt Lake, Toole, Utah, and Juab
Counties (U.S. Department of
Agriculture (USDA) 2008, p. 2; U.S.
Census Bureau (USCB) 2005a, p. 1).
These areas do not overlap the species’
gross range.
The majority of white-tailed prairie
dogs in Utah occur in the Uinta basin
(Lupis et al. 2007, p. 17). The potential
for future urban development in the
Uinta Basin is associated largely with
the city of Vernal (USCB 2005a, p. 1).
Vernal is a support and staging area for
the oil and gas development (see Factor
A. Oil and Gas Exploration and
Development) of the Uinta basin;
increased urbanized development is
primarily the result of increased oil and
gas expansion. However, much of the
required urban infrastructure is already
in place, and the majority of gross range
in Utah is managed by Federal agencies
(Table 1, above). The gross range and
mapped occupied habitat of the whitetailed prairie dog in the Uinta basin
does not overlap the developing areas
associated with the city of Vernal; thus
we expect that most of the predicted
development through 2030 will occur
outside of the species’ gross range.
We evaluated the likely centers for
urbanization in Utah through 2030 and
compared these to the gross range and
mapped occupied habitat of the whitetailed prairie dog. Based on our
evaluation, we do not consider
urbanization to be a significant threat to
the species in Utah now or in the
foreseeable future.
Wyoming
Wyoming has the largest amount of
white-tailed prairie dog habitat and the
smallest amount of predicted
development. Over 46 percent of the
species’ gross range occurs in counties
with no urban development: Park, Big
Horn, Washakie, Hot Springs, Sublette,
and Carbon Counties (USCB 2005b, p.
1). Only localized, small portions of the
remaining counties will be impacted in
the metropolitan area of Casper and the
micropolitan areas of Riverton,
Evanston, Rock Springs, and Laramie
(USCB 2005b, p. 1). Given these factors,
we do not believe urbanization is a
significant threat to the species in this
State now or in the foreseeable future.
In summary, habitat loss and
fragmentation due to urbanization may
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impact the white-tailed prairie dog, but
only in localized areas. There is no
indication that there will be significant
increases in urbanization across the
species’ gross range in the future.
Therefore, we do not believe
urbanization to be a threat to the species
now or in the foreseeable future.
Agricultural Land Conversion
Agricultural land conversion is the
change in land use from any use to an
agricultural use, including crops and
pastures. Agricultural crops can benefit
prairie dogs by providing highly
nutritious forage (Crocker-Bedford 1976,
pp. 73-74; Seglund and Schnurr 2009, p.
95). However, these colonies also are
subject to additional mortality factors
including higher lethal control efforts
(see Factor B. Shooting and Factor E.
Poisoning) to protect crops (Knowles
2002, p. 12), increased habitat
fragmentation from fences and roads,
and increased urban predators (Seglund
and Schnurr 2009, p. 95).
The impact of past agricultural
conversion is difficult to determine
given how little we know about the
historical range of white-tailed prairie
dogs. Historical population declines
occurred for all prairie dog species, and
range contractions were documented for
white-tailed prairie dogs in localized
areas in Colorado and Montana
(Knowles 2002, p. 12). However, we do
not know if these losses were the result
of agricultural conversion or other
factors; it is likely that historical
population losses were the result of a
combination of impacts across the range
of the species. Agricultural land
conversion probably displaced some
white-tailed prairie dogs in areas of
Colorado and the Big Horn Basin in
Wyoming (Knowles 2002, p. 12).
Today, agriculture occurs across 3.7
percent of the gross range of the whitetailed prairie dog (Seglund et al. 2006,
p. 50). Many of the areas currently
inhabited by white-tailed prairie dogs
are arid and semi-arid with short
growing seasons (Seglund et al. 2006
pp. 4-5) and therefore have limited
potential for crops. In Colorado, the
counties containing white-tailed prairie
dogs saw a decrease in the amount of
agricultural land by an average of 37
percent between 1954 and 2002
(calculated from data in Seglund and
Schnurr 2009, p. 96). Farm land (e.g.,
crops, pasture, grazing (not including
Federal grazing permits), USDA 2009, p.
B:14) acreages have continued to
decline across all States and counties
that occur within the gross range of the
white-tailed prairie dog (see Table 3,
below). There is not a direct correlation
between the decline in farm lands and
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most widespread type of land use across
the sagebrush biome (Knick et al. 2003,
p. 616; Connelly et al. 2004, pp. 7-29;
Knick et al., in press, p. 27). However,
the intensity of grazing on all Federal
lands has declined since the early 1900s
TABLE 3. PERCENTAGE DECREASE OF (Laycock et al. 1996, p. 3).
FARM LAND, STATEWIDE AND IN
Livestock grazing can affect ecosystem
COUNTIES PARTLY OR WHOLLY CON- functions and structures, including a
TAINED WITHIN THE RANGE OF THE general decrease in grass and shrub
WHITE TAILED PRAIRIE DOG, BE- cover, total plant biomass, and rodent
TWEEN 2002 AND 2007 (USDA species diversity and richness
2009, PP. CO 316, UT 249, WY (Fleischner 1994, pp. 633-635; Jones
2000, pp. 160-161). Fencing and roads
268, 316).
associated with grazing may cause
habitat fragmentation and may directly
Counties
or indirectly cause increased mortality
Within
of prairie dogs by increasing prairie dogState
Statewide
White-tailed
Prairie Dog
vehicle collisions, creating perch sites
Range
for raptors, and providing access
corridors for predators (Call and Maser
Wyoming
12.1
14.0
1985, p. 3; Connelly et al. 2000, p. 974;
Connelly et al. 2004, pp. 1-2).
Colorado
7.6
9.5
‘‘Overgrazing’’ refers to continued
Utah
2.3
13.1
heavy grazing beyond the recovery
capacity of the forage plants (Vallentine
Average
7.3
12.2
1990, p. 329). Overgrazing causes the
palatable and preferred herbaceous
In summary, agricultural land
conversion was likely a major historical vegetation of prairie dogs to be
preferentially removed, allowing shrubs
impact on the species. However, many
and unpalatable plants to flourish.
of the areas currently inhabited are not
suitable for crop lands, and appear to be Overgrazing can facilitate the
supporting sufficient populations of the establishment of invasive species such
as cheatgrass (Bromus tectorum)
species. The effects of land conversion
(Masters and Sheley 2001, p. 503) (see
on the species are mixed, and currently
below for more information). The
very limited land is being converted to
intensity, duration, and distribution of
agricultural uses. Therefore, we do not
consider agricultural land conversion to livestock grazing are more influential on
be a significant threat to the species now rangeland condition than livestock
density (Aldridge et al. 2008, p. 990).
or in the foreseeable future.
Grazing impacts to rangeland are
Grazing
determined by the type of animal,
stocking rate, duration of grazing,
Native herbivores, such as pronghorn
antelope (Antilocarpo americana), mule season of use, and current habitat
conditions (Vallentine 1990, entire).
deer (Odocoileus hemionus), and bison
Impacts of livestock grazing on white(Bison bison), occurred in the
tailed prairie dogs are not known largely
sagebrush-steppe region prior to
because of our lack of historical species
European settlement of western States
distribution information and the lack of
(Osborne 1953, p. 267; Miller et al.
ungrazed habitats as a baseline (Seglund
1994, p. 111), and prairie dogs coet al. 2006, p. 49). Overgrazing may
evolved with these grazers. Domestic
impact prairie dogs by degrading the
livestock grazing in the intermountain
west began with the arrival of European quality and quantity of forage;
decreasing forage availability during
settlers in the 1800s. The numbers of
livestock were unregulated, and peaked important breeding, rearing, and prein the early 1900s (Oliphant 1968, p. vii; hibernation periods; and decreasing
white-tailed prairie dog reproductive
Young et al. 1976, pp. 194-195,
success and over-wintering survival
Carpenter 1981, p. 106; Donahue 1999,
(Seglund et al. 2006, p. 49). However,
p. 15; Seglund et al. 2006, pp. 49, 51),
the potential for impacts is likely to be
with an estimated 19.6 million cattle
and 25 million sheep in the West (BLM, site-specific. For example, removing
livestock from shrub-steppe habitat can
2009, pp. 1-2).
Excessive grazing by domestic
result in either an increase of species
livestock during the late 1800s and early richness (Anderson and Inouye 2001,
1900s, along with severe drought,
pp. 538, 544-545, 549-550), or a
significantly impacted sagebrush
decrease in species richness (Manier
ecosystems (Knick et al. 2003, p. 616).
and Hobbs 2007, p. 743), depending on
Livestock grazing continues to be the
site variables.
increases in other land uses, although it
is likely that the farmland has been reconverted to other rural uses, such as
grazing, or has become urbanized (see
Factor A. Urbanization).
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Grazing effects to other prairie dog
species are known to some degree.
Livestock grazing can have positive
effects on black-tailed prairie dog
colonies because of grazing’s effect of
converting mid-height and tall grasses to
short grasses improves predator
surveillance visibility (Uresk et al. 1981,
p. 200; Cable and Timm 1987, p. 46).
Overgrazing was shown to negatively
affect Utah prairie dog growth rates,
foraging ability, and survivorship
(Cheng and Ritchie 2006, p. 550). Utah
prairie dog colony extinction rates
increased as plant species richness
declined due to overgrazing (Ritchie
1999, p. 12). Heavy grazing also can
contribute to an increase in shrubs in
Utah prairie dog habitat (CrockerBedford 1976, p. 88). However, over
time, Utah prairie dogs prefer areas with
moderate grazing intensities over
ungrazed areas, because sufficient forage
remained available in the grazed plots
(Cheng and Ritchie 2006, p. 554); cattle
cannot eat plants below 2 centimeters
(0.879 in), limiting the impacts of
moderate grazing on prairie dogs.
Results from the Utah prairie dog
studies are most applicable to whitetailed prairie dogs due to similarities in
habitat preferences. Both species use
arid shrub-steppe habitats, and whitetailed prairie dogs can utilize shrub
cover for hiding (Gadd 2000, pp. 24-26).
Therefore, we assume that white-tailed
prairie dogs react to grazing in a similar
manner to Utah prairie dogs. However,
reactions to overgrazing may not be as
extreme in the white-tailed species due
to their higher shrub tolerance.
We do not have information regarding
site-specific range conditions on Federal
or non-Federal allotments that overlap
white-tailed prairie dog habitats. Range
condition data is not collected in a
manner that is biologically meaningful
for small mammals. White-tailed prairie
dogs, being a diet generalist living in
arid environments, can persist with
limited forage. It is unknown how far
range condition must deteriorate before
a habitat becomes incapable of
supporting a colony. Therefore, we do
not know how much of the habitat is
overgrazed versus moderately grazed. It
is likely that overgrazing impacts whitetailed prairie dog colonies in localized
portions across the species’ range.
However, the available literature
indicates that prairie dogs can coexist
with some level of grazing, and in some
cases, benefit from grazing. White-tailed
prairie dogs have persisted during
higher historical grazing pressures and
livestock stocking rates have declined
substantially. Therefore, we do not
consider grazing to be a significant
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threat to the species now or in the
foreseeable future.
Fire Occurrence and Suppression
The shrub-steppe habitat occupied by
the white-tailed prairie dog evolved
with infrequent fire frequency intervals
of 100 to 450 years depending on the
dominant species of sagebrush (Baker
2006, pp. 180-181). Fire suppression
activities also were infrequent (Baker
2006, p. 182) and probably had little
effect on sagebrush landscapes (Baker in
press, p. 22).
Fire ecology of sagebrush habitats has
changed since European settlement of
the West. In general, fire frequencies
have increased in lower elevation
sagebrush habitats due to (and resulting
in further) invasion of nonnative annual
grasses, such as cheatgrass (Baker 2006,
p. 178; Crawford et al. 2004, p. 8). Fire
frequencies also have increased due in
part to human activities and presence
(Miller et al. in press p. 38). Fire
frequencies have declined in higher
elevation sagebrush habitats, resulting
in the expansion of shrubs and trees
(Miller and Rose 1999, p. 557; Baker
2006, p. 178; Crawford et al. 2004, p. 8).
The number of fires and total area
burned increased from 1980-2007 in
sage-grouse habitat (Miller et al. in
press, p. 39); this overlaps much of the
white-tailed prairie dog’s gross range in
Wyoming and Colorado. However, the
habitat mosaics and effects to wildlife
resulting from fires are not well
understood and vary across the
landscape (Baker 2006, pp. 178, 183).
We do not have information specific
to the effects of fire or fire suppression
on white-tailed prairie dogs. Whitetailed prairie dogs are adapted to a
shrub-steppe grass mosaic. They use
shrubs as forage and cover from
predators (Tileston and Lechleitner
1966, pp. 31, 302; Hoogland 1981, pp.
266-268; Gadd 2000, pp. 24-26). They
feed on forbs and grasses, and these can
be increased by fire in shrubland habitat
(Pyle and Crawford 1996, p. 323; Davies
et al. 2007, p. 518).
We anticipate that the impacts of fire
to white-tailed prairie dogs will vary
locally across the species’ gross range.
In some places where fire has occurred,
shrub or pinyon-juniper invasions are
likely to occur and may reduce available
sagebrush communities for the species
(Miller and Rose 1999, p. 557). In other
cases, cheatgrass may become the
dominant plant species (Baker 2006, p.
178; Crawford et al., p. 8), reducing
preferred forage quantity and quality for
the white-tailed prairie dog. However,
the white-tailed prairie dog is able to
use the mosaic of habitats created by fire
and fire suppression activities, and thus
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we do not believe that fire occurrence or
suppression is a significant threat to the
white-tailed prairie dog now or in the
foreseeable future.
Invasive Plant Species
Invasive plant species are promoted
by intense levels of disturbance to the
environment (Masters and Shelley 2001,
p. 504), such as oil and gas
development, agriculture, and
urbanization. Invasive plant species
alter ecological processes by displacing
native species, increasing the
vulnerability of communities to more
invaders, and reducing wildlife habitat
quality (Masters and Sheley 2001, p.
503). They can be particularly damaging
in areas of low moisture, including
shrub-steppe habitats, because they
reduce water infiltration of the soil and
possess deeper roots than native
species, allowing them to use more
water and reduce nutrient availability
over time (DiTomaso 2000, p. 257). The
proliferation of exotic annual weeds
over native perennial grasses and forbs
may impact the ability of white-tailed
prairie dogs to meet their dietary needs,
especially during drought years. Utah
prairie dog colony extinction rates were
found to increase as the number of
locally occurring plant species declined
(Ritchie 1999, p. 12). Cheatgrass in
particular is widely distributed across
the gross range of the white-tailed
prairie dog. Cheatgrass creates an
altered fire regime, increasing the
amount of fire and reducing native
grasses and shrubs (Masters and Sheley
2001, p. 503). Juniper species have
invaded sagebrush habitat beginning
with European settlement (Miller and
Rose 1999, pp. 551, 555), and may result
in decreased habitat if forestation
progresses.
The main effect of invasive species is
the decrease in habitat quality and
forage. Some habitat may be lost due to
pine-juniper invasion. It is likely that
invasive species will have localized
impacts to individual white-tailed
prairie dog habitat. Presumably, a
certain amount of invasive species is
tolerable. Despite localized impacts, no
data indicate that invasive species are
threatening the species on a rangewide
scale. At this point, the available
information does not indicate that
invasive species, although present
within the gross range, are a significant
threat to the white-tailed prairie dog
now or in the foreseeable future.
Climate Change
Global surface temperatures rose
(with regional variations) during the
past 157 years, with the largest increases
occurring since the 1970s (Trenberth et
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al. 2007, p. 252). Globally, average
surface temperatures rose by 0.074
degrees Celsius (°C) plus or minus 0.018
°C (0.13 degrees Fahrenheit (°F) plus or
minus 0.03 °F) per decade during the
past century (1906 through 2005) and by
0.177 °C plus or minus 0.052 °C (0.32
°F plus or minus 0.09 °F) per decade
during the past quarter-century (1981
through 2005) (Trenberth et al. 2007, p.
253).
Similar surface temperature increases
occurred across the gross range of the
white-tailed prairie dog. The Southwest
region, including the Colorado and Utah
portion of the species’ gross range,
observed a 0.83 °C (1.5 °F) increase in
average temperatures when compared to
a 1960 to 1979 baseline (Karl et al. 2009,
p. 129). The Great Plains region
(including the Wyoming and Montana
portion of the gross range) experienced
a 0.83 °C (1.5 °F) increase over average
temperatures, compared to the same
baseline (Karl et al. 2009, p. 123).
Drought conditions across the species’
gross range were moderate to extreme
(Marshall et al. 2008, p. 274).
The timeframe over which the best
available scientific information allows
us to reliably assess the effects of
climate change is an important
consideration. Until about 2050,
greenhouse gas emissions scenarios
(reviewed in the Intergovernmental
Panel on Climate Change Special Report
on Emission Scenarios in 2000, as cited
in Ray et al. 2009, p. 8), which are an
essential component of any climate
change assessment, result in a similar
range of projections of global and
regional climate change (Ray et al. 2009,
p. 8). Temperature increases over the
next 30 to 50 years are relatively
insensitive to the emissions scenarios
used to model the projected change.
Some warming, as projected in the
greenhouse gas emissions scenarios, is
anticipated as a result of greenhouse
gases already in the atmosphere that
will influence future climate, more so
for mid-century versus late century
(Meehl et al. 2007, p. 749; Mote and
´
Salathe 2009, p. 30). The range in the
spread of the models is due both to
details in the formulation (which
includes emission scenarios) of each
individual model, and natural
variability in climate. Because increases
of greenhouse gas emissions have lag
effects on climate, and because
projections of greenhouse gas emissions
can be interpreted with greater
confidence until approximately midcentury, model projections for the next
30 to 50 years (centered on 2050) have
greater credibility than results projected
further into future. On the basis of
available information, we have
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determined that predicted climate
changes for 2025 and 2050 are more
reliable than projections for the second
half (up until 2100) of the 21st century
and as such, we consider 2050 to
represent the foreseeable future.
One scenario predicts an average
increase in annual temperature in
western North America (covering the
entire gross range of the species) of
between 1.1 to 3.4 °C (2 to 4 °F) by 2050,
compared to a 1961 to 1979 baseline in
the western United States (Smith et al.
2000, p. 29). Other predictions range
from an annual mean warming of about
1.4 to 3 °C (2.5 to 5.5 °F) by 2050 as part
of a continent-wide pattern of warming
(Ray et al. 2009 p. 15). The projections
show summers warming more (1.7 to 3.9
°C (3 to 7°F)) than winters (1.1 to 2.7 °C
(2 to 5 °F)) (Ray et al. 2009 p. 15)
Climate change will affect
precipitation. Generally, a reduction of
depth, duration, and distribution of
snowpack is expected (Solomon et al.
2007, pp. 770-772; Marshall et al. 2008,
p. 276). Precipitation is predicted to
decrease in the Southwest region (Karl
et al. 2009, p. 129), and increase in the
Great Plains region (Karl et al. 2009, p.
123). Climate change also will affect
plague ecology (please see Factor C.
Disease and Predation, below).
Recent climatic changes, including
increased temperatures and freeze-free
periods, and changes in precipitation,
are important driving forces on
ecosystems and have affected a wide
variety of organisms with diverse
geographic distributions (Walther et al.
2002, pp. 391-392; Parmesan and Yohe
2003, p. 41). Many plant and animal
species have advanced the timing of
spring events (e.g., plant flowering or
bird migration) to occur earlier in the
year and experienced a shift in
latitudinal and altitudinal range (i.e.,
movement to higher latitudes or higher
altitude) (Walther et al. 2002, pp. 391392).
The white-tailed prairie dog and its
habitat will likely be affected in some
manner by climate change. Climate
change could impact habitat quality,
which may in turn affect prairie dog
productivity. For example, higher
quality habitats promote higher weaning
success of adult and yearling female
white-tailed prairie dogs (Cooke 1993,
in Seglund et al. 2006, p. 7). We would
expect higher quality habitats to occur
in areas where rainfall is predicted to
increase. Alternatively, increased
drought in the southwestern portion of
the gross range could reduce vegetation
quality and quantity, resulting in
lowered nutrition for the white-tailed
prairie dog (Collier and Spillet 1975, p.
153; Seglund et al. 2006, p. 64). Drought
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may result in more time spent in
burrows and less time spent foraging, as
well as water-stress from lack of
succulent forage (Collier and Spillet
1975, p. 153).
Population fluctuations of whitetailed prairie dog colonies at the Coyote
Basin Subcomplex, Kennedy Wash
Subcomplex, and Snake John
Subcomplex in Uintah County, Utah,
were likely the result of drought
(Maxfield 2009, pers. comm.). The 2002
drought resulted in a decrease in
available forage for white-tailed prairie
dogs at a time when populations had
peaked. This resulted in little or no
reproduction in 2003, and a population
crash in 2004 (Maxfield 2010, pers.
comm.). Habitat conditions improved
and the colonies rebounded to predrought population levels by 2008-2009
(Seglund et al. 2006, p. 101; Maxfield
2010, pers. comm.), indicating a level of
resiliency of this species to withstand at
least short-term climatic variations.
Life-history characteristics of the
white-tailed prairie dog may be
responsible for its resiliency and may
provide protection from effects of
climate change. The burrowing and
hibernating behaviors of prairie dogs
provide protection in times of low
resource availability and unfavorable
conditions, including those associated
with climate change (Liow et al. 2009,
pp. 264, 270). Overwinter survival and
reproductive success is linked to habitat
quality (Rayor 1985, p. 2839), so lack of
adequate food resources during drought
leads to a decrease in reproductive
output as seen above. Individual
animals also may adapt by becoming
mostly inactive during times of drought
(Liow et al. 2009, p. 270).
Shifts in the geographic ranges of
wildlife have occurred as an effect of
climate change (Walther et al. 2002, pp.
390-391), and may thus be anticipated
for the white-tailed prairie dog. Due to
the large gross range of the species (from
the Southwest to the Great Plains,
which are projected to have much
different impacts from climate change,
as discussed above), we expect the
effects of climate change to vary
throughout the species’ gross range,
both in nature of the impact and the
timing of these effects. In addition, the
species’ gross range is contained within
a region that already witnesses climatic
variability as climate varies
considerably between years (Smith et al.
2000, p. 224). Therefore we expect the
effects of climate change to vary
temporally (year-to-year) as well. This
variation in effects will buffer the
cumulative effects of climate change on
the species as a whole because only a
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portion of the gross range will be
impacted at a given time.
Although the white-tailed prairie dog
will likely be affected by climate
change, it is not apparent that a net loss
in occupied habitat will result.
Variation in conditions across the gross
range and a possible gross range shift
could maintain sufficient habitat for the
species. The species is adaptable to a
wide array of climes, as evidenced by a
geographic range that includes four
States, as well as a wide elevational
distribution (see Ecology and Life
History, above). Unlike more vulnerable
species in polar, coastal, and alpine
ecosystems, habitat space exists to
accommodate shifts in range. Therefore,
we do not believe that climate change
poses a threat to the species now or in
the foreseeable future. The relationship
between climate change and plague is
discussed in more detail below (see
Factor C. Disease or Predation).
Summary of Factor A
Energy development, urbanization,
agricultural conversion, grazing, fire
suppression, introduction of invasive
plant species, and climate change
within the gross range of the whitetailed prairie dog have occurred and
will continue to occur in the future. We
do not expect oil shale, tar sands, coal,
and other mineral extraction activities
to impact a large portion of the species’
gross range. Urbanization will have an
effect on some local populations,
particularly in Colorado, but is not
considered a rangewide threat. Grazing
is likely impacting some areas of
habitat, but no evidence indicates it is
a significant threat. A net loss of habitat
is not expected to result from climate
change. Oil and gas development has
the most potential to impact the species
due to its widespread distribution and
magnitude, yet the intensity of these
activities varies greatly across the range
due to differences in well density and
spacing. Robust colonies and complexes
exist even in the most developed areas.
The majority of the gross range has not
been subject to the intensity of
development witnessed around robust
colonies of Coyote Basin and Wolf
Creek. While further development will
occur, we expect the majority to occur
in areas with high potential for
productivity. Therefore, we do not
consider oil and gas to be a significant
threat to the species. We have no
indication that invasive plant species
are a significant threat to the whitetailed prairie dog now or in the
foreseeable future.
We conclude that the best scientific
and commercial information available
indicates that the white-tailed prairie
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dog is not now, or in the foreseeable
future, threatened by the present or
threatened destruction, modification, or
curtailment of its habitat or range to the
extent that listing under the Act as an
endangered or threatened species is
warranted at this time.
Factor B. Overutilization for
commercial, recreational, scientific, or
educational purposes.
White-tailed prairie dogs were
historically subjected to recreational
hunting and shooting as a form of pest
management on ranch and agricultural
land; these practices continue under
State regulations (see Factor D.
Inadequacy of Existing Regulatory
Mechanisms).
The effects of recreational shooting on
white-tailed prairie dogs have not been
examined. We do have limited
information on how shooting affects
black-tailed prairie dog populations.
Black-tailed prairie dogs in colonies
subject to hunting spent more time in
alert behaviors and less time foraging,
although this effect decreased a year
after shooting (Pauli and Buskirk 2007,
p. 1223). Recreational shooting reduced
black-tailed prairie dog density at
specific sites (Vosburgh and Irby 1998,
pp. 366–367; Knowles 2002, p. 14) and
may negatively affect reproductive rates
(Pauli and Buskirk 2007, p. 1228).
However, recovery of black-tailed
prairie dog populations following
shooting occurs (Knowles 1988, p. 54).
No research has evaluated long-term
impacts from recreational shooting,
although population viability
monitoring suggests it is unlikely to lead
to extinctions of even small populations
(Seglund and Schnurr 2009, p. 167).
Life-history traits and species
distribution are likely to mediate the
effects of shooting on white-tailed
prairie dogs. The majority of blacktailed prairie dogs do not reproduce
until 2 years of age (Hoogland 2001, p.
920). White-tailed prairie dogs, as
previously stated, reach maturity at 1
year of age. Thus, we believe that whitetailed prairie dog populations may be
able to recover from the effects of
shooting more quickly than black-tailed
prairie dogs.
Human recreationists may prefer
targeting black-tailed prairie dogs
because they live in larger, denser, more
identifiable colonies and their mounds
are more conspicuous (Seglund et al.
2006. p. 55). White-tailed prairie dogs
are more dispersed on the landscape
and use shrubland habitat for cover
from predators. As a consequence, they
may be more difficult to find and
successfully shoot (Grenier 2009, pers.
comm.), limiting the number of
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recreationists targeting white-tailed
prairie dog colonies.
Recreational hunting is permitted
rangewide, but it is unlikely that all
colonies are exposed to equal risk.
Recreational hunting is concentrated on
colonies with reasonably easy access
(Gordon et al. 2003, p. 12). Colonies at
higher elevations or in remote areas may
never receive hunting pressure due to
the difficulty in gaining access. Colonies
in close proximity to urban areas and
agricultural fields likely receive the
greatest shooting pressure (Gordon et al.
2003, p. 12; Seglund et al. 2006, p. 33).
Urban and agricultural land uses affect
a small part of the species’ gross range
(see Factor A).
The reproductive cycle of prairie dogs
may influence impacts of recreational
shooting. Lactating females spend the
most time above ground, and lactation
occurs during the months of April
through July (Tileston and Lechleitner
1966, p. 301). During this time, adult
male activity decreases. Recreational
hunting in April, May, and June may
have the greatest population level
impacts because pregnant and lactating
females and young of the year are the
most vulnerable (Vosburgh and Irby
1998, p. 369; Keffer et al. 2000, p. 7).
Recreational shooting could remove
more offspring than adults or artificially
skew the population sex ratio. Thus,
seasonal restrictions may be important
to reduce the effects of shooting at
localized sites.
Seasonal white-tailed prairie dog
hunting regulations are implemented in
Utah and Colorado. In Utah, shooting is
not permitted on white-tailed prairie
dog towns between April 1 and June 15
(Utah Division of Wildlife Resources
(UDWR) 2007, p. 4). In Colorado,
shooting is not permitted on public land
between March 1 and June 15 (Colorado
Division of Wildlife (CDOW) 2009, p.
10). These closures may reduce impacts
to the demographic structure and are
expected to provide protection to whitetailed prairie dog populations (Seglund
and Schnurr 2009, p. 165).
Recreational and pest removal
shooting of white-tailed prairie dogs is
allowed without a permit across much
of the species’ gross range; only
Colorado requires a license. Because
permits are not required, quantifying the
number of prairie dogs killed by
shooting is difficult. The only data
available are from Colorado’s Harvest
Information Program (CDOW 20012005). In this program, a random survey
of registered hunters was performed and
an estimated take extrapolated from the
survey results. This program does not
differentiate between species of prairie
dog, so estimates include Gunnison’s,
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black-tailed, and white-tailed prairie
dogs.
According to the data in Colorado’s
2000-2005 Small Game Harvest Reports,
prairie dogs are not a common target
among hunters. Only 4.6 to 7.4 percent
of hunters reported shooting prairie
dogs (CDOW 2001-2005). In addition, as
previously discussed, the majority of
hunted prairie dogs are likely to be
black-tailed and Gunnison’s prairie
dogs, not white-tailed prairie dogs.
Therefore, we do not believe this
represents high hunting pressure on
white-tailed prairie dogs.
Summary of Factor B
White-tailed prairie dogs, due to their
distribution and life-history
characteristics, are likely less affected
by shooting than other species of prairie
dogs. Effects of recreational shooting
may be high on specific, easily
accessible, localized colonies. However
we do not expect that these effects will
occur equally across the species’ gross
range or significantly threaten the
species as a whole.
There are no other known threats due
to commercial, scientific, or educational
uses of this species. We conclude that
the best scientific and commercial
information available indicates that the
white-tailed prairie dog is not now, or
in the foreseeable future, significantly
threatened by the overutilization for
commercial, recreational, scientific, or
educational purposes.
Factor C. Disease or predation.
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Sylvatic Plague
Sylvatic plague (plague) is an exotic
disease foreign to the evolutionary
history of North American prairie dogs.
Plague was first observed in wild
rodents in North America near San
Francisco, California, in 1903 (Eskey
and Haas 1940, p. 1), and was first
confirmed in white-tailed prairie dogs
in 1936 (Eskey and Haas 1940, p. 14).
It now occurs throughout the entire
species’ gross range (Biggins and Kosoy
2001, p. 906; Pauli et al. 2006, p. 3).
Plague is caused by a bacterium
(Yersinia pestis), which fleas acquire by
biting infected animals and
subsequently transmit via a bite to other
animals (Gage and Kosoy 2005, pp. 516517). The disease also can be
transmitted through pneumonic
(airborne) or septicemic (blood)
pathways from infected to disease-free
animals (Barnes 1993, p. 28; Ray and
Collinge 2005, p. 203; Cully et al. 2006,
p. 158; Rocke et al. 2006, p. 243; Webb
et al. 2006, p. 6236).
Plague occurs in prairie dog colonies
as enzootic and epizootic events.
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Enzootic plague is an infection
maintained in the population over time
and causes a low rate of mortality
within the colony. Not all individuals
are affected because the low density
within a colony results in less contact
between individuals and a reduced
transmission rate. Epizootic plague
occurs when the disease spreads from
enzootic hosts to more susceptible
animals, resulting in a rapidly spreading
die-off cycle (Barnes 1993, p. 29; Biggins
and Kosoy 2001, p. 909; Cully and
Williams 2001, p. 900; Gage and Kosoy
2005, pp. 506-508). Large numbers of
animals can die within a few days
(Lechleitner et al. 1962, pp. 190-192;
Cully 1993, pp. 40-42).
The factors that cause a change from
an enzootic to epizootic cycle are still
being researched, but may include host
density, flea density, and climatic
conditions (Cully 1989, p. 49; Parmenter
et al. 1999, p. 814; Cully and Williams
2001, pp. 899–903; Enscore et al. 2002,
p. 186; Lomolino et al. 2003, pp. 118–
119; Stapp et al. 2004, p. 237; Gage and
Kosoy 2005, p. 509; Ray and Collinge
2005, p. 204; Stenseth et al. 2006, p.
13110; Adjemian et al. 2007, p. 372;
¨
Snall et al. 2008, p. 246). Plague cycles
(e.g., epizootic, recovery, enzootic) may
result in successive population peaks
that are progressively lower than the
previous peak and that with each new
epizootic, the loss of colonies from
plague will exceed the rate of
establishment of new colonies (Knowles
2002, p. 13). However, this pattern of
progressively lower peaks has not been
consistently observed throughout
significant portions of the species’ gross
range.
White-tailed prairie dogs are
extremely susceptible to plague
(Williams 1986, p. 4). Individual colony
population declines of 85 to 96 percent
were reported throughout the species’
gross range following epizootic plague
events (Anderson and Williams 1997,
pp. 702, 729). Recovery of white-tailed
prairie dog colonies post-plague has
occurred within as little as 1 to 2 years
(Anderson and Williams 1997, p. 728;
Menkens and Anderson 1991, p. 330;
Anderson and Williams 1997, p. 728;
Seglund et al. 2006, p. 69), or can take
greater than 10 years (see site
discussions below, particularly Little
Snake). Epizootic plague frequently
recurs in colonies (Barnes 1993, p. 29;
Cully 1993, p. 39).
Plague likely persists in prairie dog
colonies as an enzootic even when an
epizootic outbreak subsides. In the
absence of epizootic events, plague was
found in fleas, plague antibodies were
found in prairie dog and carnivore
blood serum samples, and dead plague-
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positive prairie dogs were found
(Biggins et al. in press, p. 7). More
evidence of enzootic plague acting in
populations of prairie dogs and of blackfooted ferrets is an increase in
survivorship when treated with
experimental vaccines and flea control,
even in the absence of epizootic plague
outbreaks (Matchett et al. 2009 in
Biggins et al. in press, p. 7). Increased
survival with these treatments
compared with untreated areas is
indicative that enzootic plague is
frequently present and suppressing
population levels in untreated areas.
Possible reasons for maintenance of
plague as an enzootic in the
environment include survival of the
bacterium in the soil, persistence of the
bacterium in fleas, and the continued
slow transmission of the bacterium
within the prairie dog community (Gage
and Kosoy 2006 in Biggins et al. in
press, p. 2). Infected fleas exist in
burrows for up to 13 months following
a plague event (Fitzgerald 1993, p. 57).
Impacts of long-term enzootic plague
infection may include local extirpation
of colonies, extreme fluctuations in
densities and occupied habitat, and
inbreeding (Seglund et al. 2006, p. 58).
Enzootic plague also may alter
ecological processes (Biggins 2003, p. 7),
such as population dynamics and
dispersal. For example, if plague results
in higher mortality of adults than
juveniles, the remaining juveniles
would be less likely to disperse away
from their native colonies; they would
instead replace the adults in the native
colony, resulting in a younger
population (Biggins et al. in press, pp.
2, 7).
We lack an understanding of how
plague is impacting the white-tailed
prairie dog on a rangewide basis. Plague
monitoring is not performed rangewide.
To assess the effects of plague, we
evaluated available population and
trend data on colonies and complexes
known or suspected to be affected by
plague. Sharp declines in abundance are
generally attributed to epizootic plague
outbreaks in the absence of testing. No
data was available before the 1980s; all
available data were collected after
introduction of plague, in what we
consider to be a post-plague
environment. Therefore, recovery is
defined as a return to observed
population highs and not a return to
pre-plague (prior to 1936 when it was
first observed) abundance. We
previously defined persistence as the
long-term continuance of white-tailed
prairie dog colonies, at a high enough
level to exist in the long-term with
minimal management assistance (i.e.,
dusting, the application of insecticides
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to control flea populations, to reduce
the spread of plague), in a variety of
locations across the species’ gross range.
We recognize that different
methodologies were used at different
times and in different locales to derive
the various historical estimates we
obtained for review. These estimates
contribute to the best available
information, and we consider them
comparable for determining long-term
population trends, while acknowledging
potential error margins.
Evaluating the data is difficult due to
differences in survey methodologies.
Information available for various
colonies is alternately presented as
surveys of active burrows, occupied
habitat, population estimates, or prairie
dog counts. For this reason, comparison
between colonies is not appropriate, and
we review each colony individually to
derive a general understanding of
plague effects. Available data for several
colonies includes estimated prairie dog
populations and prairie dog counts for
different years; these figures are not
directly comparable but still describe
general trends.
Much of the available data is for sites
that were considered for black-footed
ferret management areas, which often,
but not always, represent the most
robust of the known white-tailed prairie
dog colonies. Data collected at many of
these sites was intended to determine
suitability for black-footed ferret
reintroduction, and not specifically
designed to measure prairie dog
abundance. The following is a
discussion of some examples of whitetailed prairie dog complexes that have
been impacted by plague. Some have
declined and maintain lower numbers
(appear to still be in a period of
decline), while other complexes have
declined but either partially or fully
recovered. We believe population
numbers in colonies or portions of
colonies will continue to fluctuate
widely, but retain the capacity to return
to pre-epizootic numbers.
Little Snake Complex, Moffat County,
Colorado
Plague was documented at this
complex in 1994 and 1995, following
notable declines in populations in 19831987 and again in 1993 (USFWS 1995,
p. 11). In 1995, white-tailed prairie dog
populations were estimated to equal 60
percent of levels prior to the 1983
epizootic (USFWS 1995, p. 11). Mapped
occupied habitat declined by 92 percent
between 1994 and 1999 (Seglund et al.
2006, p. iii). A portion of the complex
representing 20 percent of the total area
was remapped in 2009. Occupied
habitat in that area was 11 percent of the
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area mapped in 1989 (Ausmus 2010,
pers. comm.). Population trends in the
remaining 80 percent of the complex
were not yet assessed. No dusting (for
flea control) is performed at this site. In
summary, dramatic declines have
occurred at the Little Snake Complex.
We cannot document any recovery of
the colony to date based on this limited
information. The amount of occupied
habitat has declined since the detection
of plague in the mid-1990s.
Wolf Creek Complex, Moffat and Rio
Blanco Counties, Colorado
Plague was suspected in 1985, due to
white-tailed prairie dog declines. By
1994, the prairie dog population
rebounded to pre-1985 levels (Seglund
et al. 2006, p. 20). In 2001, population
numbers at the Wolf Creek ferret
management area were 52 percent lower
than in 1993-1994. Populations
remained stable through 2002 and 2003
(Seglund et al. 2006, p. 93), and
densities increased from 2004 to 2006
(Seglund and Schnurr 2009, p. 72).
Wolf Creek was again heavily affected
by plague in 2008, and the colony was
treated with an insecticide for flea
control in fall of 2008 and 2009 (Holmes
2010a, pers. comm.). Active colonies
remain in the complex. Quantitative
population estimates will not be
available until fall 2010 (Rustand 2010,
pers. comm.). In summary, white-tailed
prairie dog populations at the Wolf
Creek Complex have shown dramatic
declines followed by recoveries.
Fluctuations are likely related to
climatic conditions, disease, or a
combination of both (Holmes 2008 in
Seglund and Schnurr 2009, p. 72).
Dinosaur National Monument, Moffat
County, Colorado
A large white-tailed prairie dog
colony occurred at the National
Monument. No prairie dogs were
observed on the colony in 2009. The
colony is near Wolf Creek and may be
affected by the same epizootic plague
outbreak (Holmes 2010a, pers. comm.;
Holmes 2010b, pers. comm.)
Montana
Montana Fish, Wildlife and Parks
(MFWP) has records of 31 white-tailed
prairie dog colonies historically
occurring in the State (Begley 2010b,
pers. comm.). In 1997, only two colonies
remained (FaunaWest 1998 in Knowles
2002, p. 15). Three of these colonies
were permanently lost to urbanization
(Begley 2010b, pers. comm.). The cause
behind the loss of the remaining 26 is
unknown, although poisoning and
plague are potential causes (Begley
2010c, pers. comm.). In 2006, the total
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number of colonies had increased to 10.
In 2009, there were eight known active
colonies (MFWP 2009a, p. 1; Hanebury
2009, pers. comm.). Plague was
suspected by State biologists in the
disappearance of one colony from 20062009. We do not have population
numbers or trend information for any of
the Montana colonies.
Shiner Subcomplex, Uintah County,
Utah
White-tailed prairie dog population
estimates in Shiner Basin were 15,065
in 1997; 47,551 in 1998; 5,383 in 1999,
and 13,707 in 2000 (Seglund et al. 2006,
p. 101). Total animals were counted on
transects (not extrapolated for the area)
between 2002 and 2007, and estimates
were 5,475 animals in 2002; 4,284 in
2004; and 6,124 in 2007 (Maxfield 2009,
pers. comm.). In summary, white-tailed
prairie dog populations in this area have
fluctuated since 1997. The population
appears to be lower than occurred in
1998, but has stabilized since 2002.
Plague was suspected in this decline
(Maxfield 2010, pers. comm.).
Cisco Desert, Southeastern Utah
Mapping and burrow density
estimates were conducted for whitetailed prairie dogs from 1985 to 1986.
The area was resurveyed using counts of
individuals in 1991 and 1992, because
of concerns that prairie dog colonies
may be declining (Seglund et al. 2006,
p. 30). Substantially more prairie dogs
were counted during 1992 than in 1991
(Seglund et al. 2006, p. 30). The
population was estimated to be 50,000
animals in 1997 followed by apparent
declines in burrow activity in 2001
(Wright 2006, p. 3). Between 1985 and
2006, burrows detected on transects
dropped from 48.8 per ha (120.6 per ac)
to 37.1 per ha (91.8 per ac). Of the
individual complexes, 14 increased in
density while 31 decreased (Wright
2006, p. 7).
We interpret this to represent an
overall decline in this area between
1985-2006, with marked fluctuations
during this period. Plague is suspected
in these declines, although drought also
contributed (Wright 2006, p. 3). The
white-tailed prairie dog is still
considered widespread and abundant in
this area (Wright 2006, p. 3).
Meeteetsee Complex, Park County,
Wyoming
Plague was first documented at
Meeteetsee in 1985 (Biggins 2003, p. 7).
Large fluctuations in population
estimates and active burrows occur at
this complex. For example, total active
burrows counted were 12,481 in 1985;
7,644 in 1989; 6,782 in 1997; 12,428 in
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1990; and 16,736 in 1998 (Biggins 2003,
p. 11). This complex was resampled in
2008, and numbers were higher than
1997, but still below 1980s values
(Biggins 2010, pers. comm.). In
summary, individual colonies within
the complex appear to suffer local, large
population collapses followed by
subsequent recoveries (Biggins et al. in
press, p. 2). White-tailed prairie dogs
continue to occupy the Meeteetsee
Complex.
Shirley Basin/Medicine Bow Complex,
Wyoming
Population estimates for the complex
are available, based on partial surveys.
Therefore, numbers presented represent
trends but are not directly comparable.
Numbers in parenthesis are the percent
of complex transected during that year.
Population estimates were 30,389 (31)
in 1991; 14,551 (22) in 1993; 5,916 (6)
in 1994; 19,876 (19) in 1996; 6,547 (16)
in 1998; 6,669 (16) in 2000; and 34,698
(8) in 2001 (Seglund et al. 2006, p. 107).
An additional 38,756 white-tailed
prairie dogs also were recorded in 2001,
in an area of the complex not surveyed
in the previous years (Grenier et al.
2002, p. 23). Mapped occupied habitat
increased 25 percent between 1991 and
2006 (Grenier et al. 2007, p. 133).
Similar to other complexes, white-tailed
prairie dog populations at Shirley Basin
fluctuate dramatically, although direct
comparisons are not appropriate due to
yearly variation in transect sites. Plague
was first documented at Shirley Basin in
1987 (Seglund et al. 2006, p. 36). In
summary, plague likely impacted
populations at Shirley Basin (Seglund et
al. 2006, p. 36) and may be responsible
for the fluctuating populations.
The examples above clearly show that
plague is present within white-tailed
prairie dog colonies across the species’
gross range, and is likely responsible for
large population fluctuations and
significant declines in complexes or
portions of complexes. However, the
colonies and complexes also show a
capacity to recover after plague events.
Some colonies decline and maintain
lower numbers, perhaps due to enzootic
plague (Little Snake, Montrose County,
and Shiner Basin). Other complexes
decline but either partially recover
(Montana colonies, Wolf Creek, Cisco
Desert) or fully recover (Shirley Basin/
Medicine Bow).
We do not know if the colonies and
complexes recovered to population
numbers that existed before plague was
introduced because we do not have
historical population information. We
also do not know if the colonies and
complexes exhibit pre-plague lifehistory patterns of mortality,
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reproduction, dispersal, and
colonization. The available data
indicates that white-tailed prairie dogs
can continue to persist in the presence
of plague. Population numbers in
colonies or portions of colonies will
continue to fluctuate widely, but retain
the capacity to return to pre-epizootic
numbers. Plague is demonstrated to
cause this pattern in rodent species in
Asia, where plague is native (Biggins
and Kosoy 2001, p. 64).
Continued persistence of colonies
rangewide is impacted by many factors.
The separation of colonies within
complexes and distance between
colonies may mediate the spread of
plague. For example, the slow
population decline witnessed at
Meeteetsee between 1989 and 1997 is
likely the impact of plague affecting
only a portion of the complex at a time
(Biggins et al. in press, p. 2). Similarly,
only a portion of Wolf Creek was
affected by plague while the nearby
Crooked Wash did not experience a
concurrent decline (Holmes 2010b, pers.
comm.). Finally, a population at the
Arapaho National Wildlife Refuge in
north-central Colorado did not decline
concurrent with the decline at Wolf
Creek (Hoogland 2010, pers. comm.).
The ability for white-tailed prairie
dogs to migrate may promote
recolonization of colonies impacted by
plague (Seglund et al. 2006, p. 10). The
ability to repopulate colonies depends
on a mosaic of interconnected colonies;
isolated colonies are less likely to
support sufficient immigration for longterm persistence of plague-affected
colonies (Seglund et al. 2006, p. 60).
The complexes of Little Snake, Wolf
Creek, Coyote Basin, Kennedy Wash,
Snake John, and Shiner are considered
separate but are all located in adjacent
Uintah and Moffat Counties, and a
reasonable amount of connectivity
exists between them.
Size also may be an important factor
regulating persistence of individual
colonies. Most of the sites discussed
above are considered large complexes.
In black-tailed prairie dogs, introduction
of plague has resulted in colonies being
consistently smaller than before first
exposure to plague (Cully and Johnson
2008, p. 12). White-tailed prairie dog
colonies may overall be smaller now
when compared to pre-plague levels.
Small colonies not part of a large
complex may be affected by plague at a
higher intensity and may not have
enough source individuals to recover.
Smaller populations are generally
accepted to be more vulnerable than
larger populations (Shaffer 1981, p.
131). Larger groups of black-tailed
prairie dogs had a higher survival
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probability after translocation than
small groups (Robinette et al. 1995, p.
872). We do not have data to assess
specifically how plague operates in
smaller, more isolated colonies.
However, population viability modeling
in black-tailed prairie dogs
demonstrated continued persistence in
small, fragmented colonies, assuming
connectivity between populations
(George et al. 2008, p. 1).
The temporal nature of plague is an
important factor when considering
rangewide impacts (Seglund et al. 2006,
p. 59). Plague does not impact all
populations rangewide at the same time,
with a predictable reoccurrence rate, or
to the same intensity. Large plaguerelated population declines were
witnessed across the gross range, but in
different years: Montana in 1997;
Shirley Basin/Medicine Bow, Wyoming,
in 1994 and 1998; Wolf Creek, Colorado,
in 2001/2002 and 2008; and Uintah
Basin in 1999 and 2003/2004.
Some social and behavioral traits of
white-tailed prairie dogs appear to favor
their long-term persistence in a plague
environment. White-tailed prairie dog
colonies are less dense and more widely
dispersed than black-tailed or
Gunnison’s prairie dog colonies, which
may slow transmission rates (Cully
1993, pp. 40-41; Cully and Williams
2001, pp. 898-899). White-tailed prairie
dogs are less social when compared to
other species; this trait may reduce
transmission among individual animals
(Hoogland 1981, pp. 252-253; Cully
1993, p. 40). Hibernation also
contributes to slower transmission rates,
although this may simply delay the
onset of symptoms throughout all the
colonies (Barnes 1993, p. 35).
Some tools are available to control
plague. Deltamethrin and pyraperm are
two insecticides used to successfully
control fleas on colonies of different
prairie dog species (Seery et al. 2003,
entire; Hoogland et al. 2004, entire). Use
of these insecticides has increased the
number of juvenile Utah prairie dogs
weaned (Hoogland et al. 2004, p. 379)
and resulted in higher survival rates for
black-tailed, white-tailed, and Utah
prairie dogs (Biggins et al. in press, p.
5). Currently, insecticide use on whitetailed prairie dog colonies is limited to
experimental use and when plague
appears to be impacting colonies that
support black-footed ferret
reintroduction sites. Wolf Creek was
treated in the summer and fall of 2009,
in conjunction with that outbreak, and
likely will be treated again in 2010.
Other sites with black-footed ferrets
include Coyote Basin, Snake John,
Shirley Basin/ Medicine Bow, and
Meeteetsee. Due to the expense of
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applying insecticide and the effects to
non-target species, this method is only
used when plague has already been
detected.
Experimental vaccine-laden baits are
in development to immunize prairie
dogs against plague. Black-tailed prairie
dogs exposed to plague in a lab setting
and fed vaccine baits experienced a high
rate of survival (Mencher et al. 2004, pp.
5503-5504, Rocke et al. 2008, pp. 933,
936). The effectiveness of the vaccine is
scheduled for field testing over the next
year. A systemic flea control bait also is
under development (Poche et al. 2008,
entire). The flea control bait reduces flea
loads on animals, the primary vector in
spreading plague in prairie dogs
(Jachowski 2009, entire). While use of
any of the above techniques, or
combinations thereof, to manage plague
has not been tested at the landscape
level, these techniques show promise in
the ability to manage plague.
The occurrence of plague may be
affected by climate change. As
discussed in Factor A, Wyoming and
Montana’s yearly precipitation will
become more variable while
temperatures are expected to increase
rangewide over the next 40 years.
Plague outbreaks are significantly
correlated with increased rainfall,
particularly spring rainfall (Stapp et al.
¨
2004, p. 237; Snall et al. 2008, pp. 245246). However, plague outbreaks are
negatively correlated with the yearly
total number of hot days and overall
increased temperatures (Stapp et al.
¨
2004, p. 238; Snall et al. 2008, p. 245).
Because climate change will likely
produce variation in annual rainfall
(Stapp et al. 2004, pp. 504-505), plague
outbreaks may oscillate as these factors
interact. Warmer winters in particular
can result in increased plague
transmission (Stapp et al. 2004, p. 236;
Salkeld and Stapp 2008, p. 620). This
effect is probably due to a range of
factors including reduced hibernation
(Rayor 1985, p. 195), better over-winter
flea survival, and increased habitat
productivity (Stapp et al. 2004, pp. 237238). In the Colorado and Utah portions
of the gross range, winter precipitation
is expected to vary greatly from year to
year, with some winters being very dry
while others experience intense
precipitation and flooding (Karl et al.
2009, p. 130). This variation may result
in pulses of winter or early spring
plague outbreaks during wetter years
that are reduced in intensity over
several years as hotter summer
temperatures reduce plague in the
environment. Plague occurrences are
likely to decrease in black-tailed prairie
¨
dogs due to climate change effects (Sna
ll et al. 2009, p. 505). Because it is
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believed that changing environmental
conditions resulting from climate
change is directly impacting plague
transmission, we also may expect that
plague will eventually decrease in
white-tailed prairie dog habitats,
concurrent with rising temperatures.
Climate change may have less of an
impact on plague levels if white-tailed
prairie dogs exhibit a range shift as
witnessed in some other species.
Tularemia and Monkeypox
Tularemia (Francisella tularensis) and
monkeypox (Orthopoxvirus spp.) are
diseases that have had impacts on
captive black-tailed prairie dogs
associated with the pet trade, and a wild
black-tailed prairie dog was reported as
having fallen victim to West Nile virus
(Seglund et al. 2006, p. 58). We have no
information to indicate that any of these
diseases are a concern for white-tailed
prairie dogs at the population or species
level.
Predation
Many species prey upon the whitetailed prairie dog including black-footed
ferrets (Mustela nigripes), hawks
(Accipiter, Micronisus, Melierax,
Urotriorchis and Megatriorchis spp.),
eagles (Haliaeetus spp.), badgers
(Taxidea taxus), and coyotes (Canus
lupis) (Seglund et al. 2006, p. 58).
However, predation is a natural
occurrence for white-tailed prairie dogs,
and we have no information to indicate
that predation is a threat to the species.
Summary of Factor C
Plague occurs throughout the gross
range of the white-tailed prairie dog.
The rangewide and long-term effects of
plague on prairie dog populations are
not well understood. There is evidence
of epizootic outbreaks of the disease and
enzootic maintenance of the disease in
prairie dog colonies. We acknowledge
that populations are probably reduced
from historic levels, and some colony
behavioral functions, including
migration and social interactions, may
be impaired by plague. However, we
have no evidence that demonstrates that
plague has eliminated white-tailed
prairie dogs from large portions of its
gross range after over 70 years of
exposure to the disease. Affected
colonies have shown partial or complete
recovery after plague events, and
complexes continue to persist at the
landscape level. Available information
indicates that plague events are to some
extent localized temporally and
spatially, which may help mediate the
species-level effects. Management
actions are underway to research and
implement plague control mechanisms,
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such as dusting, vaccines, and flea
control, which should help alleviate
colony population fluctuations and
declines due to plague in the foreseeable
future. As a result, we have determined
that while plague is affecting the whitetailed prairie dog, it is not a significant
threat that is now causing or projected
to cause the species to be at risk of
extinction.
The available evidence does not
indicate that other diseases or predation
are sufficiently acting on the species to
threaten the species with possible
extinction now or in the foreseeable
future. We conclude that the best
scientific and commercial information
available indicates that the white-tailed
prairie dog is not now, or in the
foreseeable future, threatened by disease
or predation to the extent that listing
under the Act as an endangered or
threatened species is warranted at this
time. Continued plague monitoring and
research will be important for us to
continue to assess the level of impact
this disease plays in the long-term
conservation of white-tailed prairie
dogs. The development of a vaccine to
protect prairie dog populations may
help decrease future effects of plague.
Factor D. The inadequacy of existing
regulatory mechanisms.
State Regulations and Private Land
Management
Rangewide
State laws and regulations may
impact white-tailed prairie dog
conservation by providing specific
authority for white-tailed prairie dog
conservation over lands which are
directly owned by the State; providing
broad authority to regulate and protect
wildlife on all lands within their
borders; and providing a mechanism for
indirect conservation through regulation
of threats to the species (e.g., noxious
weeds). In general, States have broad
authority to regulate and protect
wildlife within their borders. All of the
States within the range of the whitetailed prairie dog have State school trust
lands that they manage for income to
support their schools. We are unaware
of any specific regulations to ensure that
the management of the State trust lands
is consistent with the needs of whitetailed prairie dog. Thus there are
currently no regulatory mechanisms on
State trust lands to ensure conservation
of the species.
Environmental planning regulations
establish environmental quality as an
essential component of land use and
project planning and provide a
structured, analytical frame work to
make decisions that balance
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environmental and economic factors
(Council on Environmental Quality
(CEQ) 1997, p.11). The implementation
of the National Environmental Policy
Act (NEPA, 42 U.S.C. 4321 et seq.) has
improved the quality of projects and
reduced impacts to the environment in
the Federal planning process (CEQ
1997, p. 17). Within the range of the
white-tailed prairie dog, only Montana
has NEPA-like environmental planning
regulations (CEQ 2009, entire). Because
activities on private and State lands in
Colorado, Utah, and Wyoming are not
subject to environmental review, they
may have a greater impact to whitetailed prairie dogs than similar activities
on Federal lands.
Potential impacts to the species that
can be managed by State or private
entities include recreational shooting,
shooting to protect agricultural interests,
and oil and gas development on nonFederal mineral estates. In addition, the
State wildlife agencies can contribute to
species conservation by supporting
research and monitoring efforts,
including plague management.
The Western Association of Fish and
Wildlife Agencies (WAFWA)
coordinates management efforts of the
white-tailed prairie dog and other
species among the western States. The
WAFWA prepared a Rangewide
Conservation Agreement for the WhiteTailed Prairie Dog in 2006 (Seglund et
al. 2006, entire). The objectives of the
conservation agreement include
identification and monitoring of the
species’ status and distribution, public
education, identification and
implementation of priority research
needs, and creation of State
management plans (Seglund et al. 2006,
p. 3). The conservation agreement
provides expertise, recommendations,
and coordination of funding for the
conservation of the species, but does not
provide regulatory protection.
Private lands comprise a large portion
of the predicted range of the species.
Private landowners can control prairie
dogs on their land as necessary in all
States. However, general public access
and hunting on private lands
throughout the gross range are limited
by trespass laws. We have no evidence
that the control activities or policies of
individual private landowners are
threatening the species.
Oil and gas development occurs
across the gross range of the species,
including on lands managed by the
States. We are unaware of any
regulations or protection measures for
white-tailed prairie dogs on these lands.
However, based on available
information, we do not consider oil and
gas development a factor that
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significantly threatens the white-tailed
prairie dog (see Factor A. Oil and Gas
Exploration and Development, above).
Colorado
The Colorado Department of Wildlife
(CDOW) released a Statewide
Conservation Strategy outlining the
management of white-tailed and
Gunnison’s prairie dogs in fall 2009
(Seglund and Schnurr 2009, entire).
This document guides the development
of conservation strategies for the three
white-tailed prairie dog Individual
Population Areas (IPAs) (see
Distribution and Abundance). Local
action plans with individual goals and
objectives are under development for
each IPA. The Statewide Conservation
Strategy provides management priorities
and guidance for the species, but does
not provide regulatory protection.
All prairie dog species are classified
as small game in Colorado. A small
game license is required for shooting
prairie dogs, with the exception of
private landowners and their immediate
family members or designees, who may
kill prairie dogs causing damage on
their lands (CDOW 2009, p. 10).
Shooting of prairie dog species is not
permitted on public land between
March 1 and June 15 (CDOW 2009, p.
10), providing protection during the
sensitive breeding and rearing time
periods.
The Colorado Oil and Gas
Conservation Commission (COGCC) had
a policy encouraging voluntary
cooperation among oil and gas operators
in preventing and mitigating potential
impacts to wildlife (COGCC 1996,
entire). In 2009 the state legislature
passed rules requiring oil and gas
companies to consult with state wildlife
officials regarding the impacts of their
proposed development to wildlife. The
rules promote best management
practices and allow the state to set
reasonable conditions of development
in sensitive wildlife areas (COGCC 2009,
entire). Application of these rules to
white-tailed prairie dogs in particular is
then up to state wildlife officials. Given
the recent passing of these rules, it is
unknown if they will be applied to
prairie dog species.
Montana
White-tailed prairie dogs are
identified as a Species of Greatest
Conservation Need (Tier 1) in Montana’s
Comprehensive Fish and Wildlife
Conservation Strategy (MFWP 2009a, p.
1). The State defines this as a species
whose needs must be specifically
addressed, whether through focus areas,
community types, or individually
(MFWP 2005, p. 188). This designation
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gives the State statutory authority to
manage the species. For example, under
this authority, MFWP translocates
white-tailed prairie dogs in an effort to
establish new colonies. Translocations
began in 2007, and are expected to
continue until at least 2011.
White-tailed prairie dogs in Montana
were once protected from all shooting,
but the regulation protecting them has
lapsed, and they are currently
unprotected. A license is not required to
hunt prairie dogs in Montana.
Utah
The white-tailed prairie dog is listed
as a Species of Concern in Utah, defined
by the State as a wildlife species for
which there is credible scientific
evidence to suggest a threat to
continued population viability within
the State (UDWR 2007, p. 1). Species are
provided this designation in order to
encourage management actions and
prevent the species from declining to
the point where listing is necessary.
Utah completed a conservation
agreement and Strategy for white-tailed
and Gunnison’s prairie dogs in 2007.
Under the conservation agreement, the
State committed to conduct occupancy
surveys in an effort to detect population
declines and respond with appropriate
management actions (Lupis et al. 2007,
pp. 22-23). The Statewide conservation
strategy provides management priorities
and guidance for the species, but does
not provide regulatory protection.
No license is required to hunt prairie
dogs in Utah (UDWR 2009, p. 1).
However, prairie dog shooting is not
allowed between April 1 and June 15
(UDWR 2009, p. 4), providing the
species with protection during sensitive
breeding and rearing periods. In
addition, a year-round shooting closure
is implemented in the Coyote Basin
black-footed ferret reintroduction area
(7,604 ha (18,789 ac)).
Wyoming
White-tailed prairie dogs are
considered a Species of Greatest
Conservation Need: Native Species
Status 4 in Wyoming. Species are given
this designation when habitat is
restricted or threatened, or population
numbers are declining and unknown.
The species was given a status level of
4 due to unknown population trends
and restricted or vulnerable but not
declining habitat (Wyoming Game and
Fish Commission 1998, p. 238). No
conservation agreement is in place for
the species in Wyoming. State biologists
participate in prairie dog surveys and
management under the guidance of
WAFWA.
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Shooting of white-tailed prairie dogs
is permitted in Wyoming without a
license (WGFC 1998, pp. 52-54), and
there are no seasonal closures. State
biologists have witnessed no negative
effects from removing a seasonal closure
on the Shirley Basin population
(Grenier 2009, pers. comm.); therefore, it
seems unlikely that lack of closures is
having a population-level effect.
In summary, the States are actively
involved in prairie dog research and
monitoring efforts under direction of the
WAFWA Conservation Agreement and
State-specific species management
plans. The information obtained
through these efforts will be valuable for
future efforts to conserve the species
and avoid threats. Recreational shooting
of prairie dogs is not considered a threat
to the species (see Factor B.
Overutilization, above). However,
seasonal shooting closures are
implemented on a site-specific basis in
Colorado and Utah. The lack of
environmental planning and protection
for the species from all land use
activities on non-Federal land,
including non-Federal oil and gas
leases, may impact the species in the
future. However, at this time the
information we do have does not
indicate that threats from land use
activities are sufficient to require
regulatory mechanisms now or in the
foreseeable future (see Factor A., above).
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Federal Management Authority
Potential impacts to the species that
could be managed by the Federal land
management agencies include oil and
gas development, grazing, fire
suppression, poisoning, and recreational
shooting.
Bureau of Land Management
The Federal Land Policy and
Management Act of 1976 (FLPMA) (43
U.S.C. 1701 et seq.) is the primary
Federal law governing most land uses
on BLM lands. Section 102(a)(8) of
FLPMA specifically recognizes wildlife
and fish resources as being among the
uses for which these lands are to be
managed. The BLM considers the needs
of wildlife, including the white-tailed
prairie dog, when conducting activities
in their habitat. Typically, this means
the impacts to these species are
considered during project planning
stages and conservation measures may
be included at the discretion of the
agency biologists. In addition, the BLM
is required to meet environmental
planning requirements under NEPA (73
FR 61292), which requires reviewing the
effects of actions on the environment
(including wildlife) before
implementation.
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The BLM’s resource management
plans (RMPs) are the basis for all of its
actions and authorizations involving
BLM-administered lands and resources.
The RMPs establish allowable resource
uses, general management practices,
program constraints and other
parameters of project design (43 CFR
1601.0–5(k)). These plans provide a
framework and programmatic guidance
for site-specific activity plans. In
addition, BLM management plans may
include conservation measures to
protect the species. These measures vary
between State and field offices.
Site-specific plans likely to affect
white-tailed prairie dogs typically
include livestock grazing, oil and gas
field development, wildlife habitat
management, and other land use
activities. The potential effects of these
activities on the species’ habitat are
addressed under Factor A, above.
In Colorado’s Grand Valley/
Uncompahgre IPA, BLM lands have
special designations offering
protections, such as a yearly closure to
motorized and non-motorized travel
restrictions to designated routes only,
and withdrawal from all forms of
mineral entry, including oil and gas
leasing (Seglund and Schnurr 2009, p.
55). The BLM-owned portion of the
Northwest IPA’s white-tailed prairie
dog’s gross range is considered high or
medium potential for oil and gas
development. The RMPs stipulating
activities in this IPA are undergoing
revisions to address oil and gas
development and associated impacts
(Seglund and Schnurr 2009, p. 61). We
do not know if the RMP revisions will
include conservation measures to
minimize the effects of oil and gas
development to white-tailed prairie
dogs. At this time, we do not believe oil
and gas development to be a significant
threat to the species (see Factor A. Oil
and Gas Exploration and Development,
above). However, the ability to
adequately monitor the species in
energy development areas will be
important for our long-term ability to
minimize impacts.
In Utah, the BLM updated several
field office RMPs in 2007. These
updated RMPs included a stipulation to
avoid surface-disturbing activities
within 201 m (660 ft) of white-tailed
prairie dog colonies in known prairie
dog habitat (BLM 2008a, p. K:13). An
exception may be granted if impacts can
be mitigated or if there is no other
reasonable location to develop the lease.
This stipulation is included in the
management plans that apply to whitetailed prairie dog colonies near Vernal,
Richfield, Price, and Moab. No
exceptions to this stipulation have yet
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been made in the Moab or Price field
offices. Vernal field office staff report
four exceptions to this stipulation. In all
examples, disturbance was limited to
the edge of a colony because no other
alternatives were available (McDonald
2010, pers. comm.). The RMP governing
activities in Rich County has not been
amended to include a stipulation to
protect white-tailed prairie dog habitat
(Madsen 2009, pers. comm.). However,
this area comprises a very small amount
of occupied habitat in Utah, and any
impacts to this area are unlikely to
produce population-level effects.
In Wyoming, no extra protections are
extended to white-tailed prairie dogs on
BLM land, although control efforts
(described below in Factor E) are not
permitted except in the case of
extensive resource damage or a threat to
human health and safety (Keefe 2009,
pers. comm.). Given the extent of oil
and gas development in this State, lack
of regulations on BLM land could be
detrimental to the species, but the
available evidence does not suggest that
impacts are rising to a significant
population-level threat (see Factor A.
Oil and Gas Exploration and
Development, above).
U.S. Forest Service (USFS)
The USFS considers the white-tailed
prairie dog to be a Region 2 sensitive
species, which requires USFS to
consider the presence of the species and
recommend mitigation when planning
projects that may affect the species
(Seglund and Schnurr 2009, p. 55).
Controlling prairie dogs with toxicants
is banned or closely controlled on USFS
lands (Seglund et al. 2006, p. 62). The
USFS manages less than 1 percent of the
total species’ gross range, so their
management strategies are unlikely to
impact the species rangewide
significantly.
U.S. Fish and Wildlife Service
The Service manages over 500
National Wildlife Refuges and their
satellites, but only about 7,975 ha
(19,706 ac) fall within the white-tailed
prairie dog’s predicted range (Seglund et
al. 2006 pp. 98, 104, 109). Management
of this species is not addressed on these
lands (Seglund et al. 2006, p. 62).
Control of prairie dogs through toxicants
on these lands is banned or closely
controlled (Seglund et al. 2006, p. 62).
Given the small amount (less than 1
percent) of predicted habitat managed
by us, the available information does
not suggest that our management
practices are having a significant impact
on the species.
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National Park Service
The NPS preserves unimpaired the
natural and cultural resources and
values of the national park system for
the enjoyment, education, and
inspiration of this and future
generations. This agency manages
13,393 ha (33,096 ac) of the white-tailed
prairie dog’s predicted range (Seglund et
al. 2006, pp. 98, 104, 109). Management
of this species is not addressed on these
lands (Seglund et al. 2006, p. 62).
Control of prairie dogs through toxicants
on these lands is banned or closely
controlled (Seglund et al. 2006, p. 62).
Given the small amount (less than 1
percent) of predicted habitat managed
by this agency, the available information
does not suggest that NPS management
practices are having a significant impact
on the species.
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Tribal Lands
The Bureau of Indian Affairs (BIA)
administers 135,376 ha (334,523 ac) of
land within the white-tailed prairie
dog’s predicted range (Seglund et al.
2006, pp. 98, 104, 109). Additional land
owned by Tribes or Tribal members may
have been included under the
calculations for private land. We are
unaware of any official policies from the
BIA or Tribal councils regarding
protection of white-tailed prairie dogs
on BIA-administered or Tribally owned
lands. Given the small amount (less
than 1 percent) of predicted habitat
managed by Tribes, the available
informationdoes not suggest that BIA
management practices are having a
significant impact on the species.
In summary, Federal agencies have
very few regulations for the protection
of this species. The oil and gas surface
use restrictions in the State of Utah
likely help minimize the impacts of oil
and gas development to white-tailed
prairie dogs. The lack of protection
measures for the species elsewhere may
impact the species in the future;
however, at this time the available
information does not indicate that factor
significantly threatens the species in the
foreseeable future (see Factor A. Oil and
Gas Exploration and Development,
above). Poisoning also is banned or
closely controlled on Federal lands (see
Factor E. Poisoning, below, for further
discussion).
Summary of Factor D
All States are involved in active
management of the species. The States’
conservation agreements and strategies,
while not regulatory documents, contain
direction to help mitigate threats to the
species.
Potential threats for which regulatory
mechanisms may play a role include oil
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dogs by 1919 (Seglund and Schnurr
2009, p. 140).
The population-level impact of this
practice is difficult to quantify due to
our lack of knowledge of the species’
historical distribution and our lack of
information on the exact locations of
poisoning efforts (Seglund and Schnurr
2009, p. 140). However, the extent of
poisoning for all prairie dog species was
extensive. For example, from 1915 to
1964, Colorado poisoned an area of
9,380,191 ha (23,178,959 ac), which was
occupied by the Gunnison, black-tailed,
and white-tailed species of prairie dogs
(Forrest 2002 in Seglund and Schnurr
2009, p. 141). Black-tailed prairie dogs
were the main target of eradication
campaigns due to their visibility on the
landscape, but Gunnison and whitetailed prairie dogs also were poisoned
(Seglund and Schnurr 2009, p. 140).
Poisoning in all States became less
common after Federal regulation of
pesticides was enacted (Seglund et al.
2006, p. iv). State and Federal agencies
are rarely involved in control efforts
unless human health and safety are at
risk. The BLM, in particular, has a
restriction against poisoning prairie
dogs unless required for human health
and safety or if resource damage meets
specified requirements. Control of
white-tailed prairie dogs in this manner
is rare, with the agency only reporting
one small area currently under control
(Keefe 2009, pers. comm.). Individual
landowners may still control prairie
dogs on their private property.
Poison applications can be an
effective means to control prairie dog
population size. Baited poisons can
result in 75 to 85 percent mortality, and
fumigants can result in 95-percent
mortality of prairie dog populations
when properly applied (Seglund and
Schnurr 2009, p.141). Although
Factor E. Other natural or manmade
factors affecting its continued existence. poisoning was historically widespread,
there is no information available to
The following potential natural or
indicate that poisoning occurs at more
manmade factors may affect the whitethan a localized scale today. We were
tailed prairie dog: (1) Poisoning, and (2) unable to quantify amount of toxicants
competition with Wyoming ground
sold for white-tailed prairie dog control.
squirrels. These factors are further
The States within the gross range of the
discussed below.
white-tailed prairie dog do not compile
records of pesticide sales. There are 103
Poisoning
licensed dealers of restricted use
Poisoning of white-tailed prairie dogs toxicants in Utah and 288 licensed
has historically occurred throughout the dealers in Colorado. The WGFD staff
species’ gross range (Seglund et. al 2006, surveyed Wyoming dealers in 2003, and
p. 63). The USDA Biological Survey and determined that toxicant sales were too
the Agriculture Appropriations Act of
small to warrant tracking, with a total
1915 (38 Stat. 1111) planned and
less than would be required to treat 400
authorized a Westside Plan to eliminate ha (1,000 ac) per year (Grenier 2009,
prairie dogs across western rangelands
pers. comm.).
White-tailed prairie dog biology may
(Oakes 2000 in Seglund and Schnurr
provide some protection from
2009, p. 140). Prairie dog poisoning
campaigns began in all States across the poisoning. Because they inhabit less
dense, widely distributed colonies, they
gross range of the white-tailed prairie
and gas development, grazing, fire
suppression, poisoning, and recreational
shooting. We have determined that
these factors do not rise to the level of
a significant threat to the white-tailed
prairie dog or its habitat rangewide.
Our evaluation determined that these
land uses may impact white-tailed
prairie dogs on a localized basis.
Existing regulatory mechanisms are
adequate to reduce impacts at these
localized levels. For example, seasonal
shooting closures in Colorado and Utah
are protecting white-tailed prairie dog
populations in some areas during
sensitive breeding and rearing time
periods. The BLM’s RMPs in Utah
contain recommendations to avoid
surface disturbance during oil and gas
development, although this does not
mediate the impact of habitat
fragmentation from this threat. In
addition, the historical threat of
poisoning was curtailed when Federal
regulation of pesticides was enacted,
and is generally not permitted on
Federal lands.
Further coordination between State
and Federal agencies would be of
benefit to this species, particularly in
managing habitat fragmentation. More
management would be of benefit to the
species, but the available evidence does
not indicate that limited management
strategies are a significant threat to the
species.
We conclude that the best scientific
and commercial information available
indicates that the white-tailed prairie
dog is not now, or in the foreseeable
future, threatened by inadequate
regulatory mechanisms to the extent
that listing under the Act as an
endangered or threatened species is
warranted at this time.
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do not attract the amount of negative
attention associated with black-tailed
prairie dogs (Knowles 2002, p. 2;
Grenier 2009, pers. comm.). In addition,
the widespread nature of white-tailed
prairie dog colonies makes control
through the use of toxicants very labor
intensive and unsuitable for widespread
control. Black-tailed prairie dogs are
known to rebound rapidly after control
efforts (Seglund and Schnurr 2009, p.
140). White-tailed prairie dogs may have
this capability as well (Seglund and
Schnurr 2009, p. 140), particularly
because they reproduce at a younger age
than black-tailed prairie dogs.
In summary, today, poisoning
generally occurs only on private land for
site-specific control purposes rather
than wide-spread population
eliminations (Seglund et al. 2006, p. 65).
White-tailed prairie dogs may have the
capability to rebound from control
efforts. Their scattered distribution and
behavioral mechanisms may provide
them with some protection from
poisoning efforts. Therefore, we do not
believe poisoning to be a significant
threat to the species now or in the
foreseeable future.
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Competition
Competition may occur between
Wyoming ground squirrels and whitetailed prairie dogs (Seglund and
Schnurr 2009, p. 100). Their diets
overlap and their burrows are often
interspersed. Wyoming ground squirrels
are found in some areas where plague
has decimated Gunnison’s prairie dogs
(Seglund and Schnurr 2009, p. 100).
However, white-tailed prairie dogs were
observed to chase and kill Wyoming
ground squirrels (Cooke 1990, p. 275).
Given their size advantage and
aggression, it seems unlikely that prairie
dogs would be excluded by Wyoming
ground squirrels (Hoogland 2009, pers.
comm.). In addition, ground squirrels
are vulnerable to plague, and epidemics
reduce their numbers alongside prairie
dogs. At this time there is no evidence
to suggest that there may be other
competitors or that competition is a
threat to the white-tailed prairie dog.
Summary of Factor E
Available evidence does not suggest
that control of prairie dogs through
poisoning is a major or increasing threat
to the while-tailed prairie dog. It seems
unlikely that competition with
Wyoming ground squirrels would
threaten the species’ persistence.
We conclude that the best scientific
and commercial information available
indicates that the white-tailed prairie
dog is not now, or in the foreseeable
future, threatened by other natural or
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manmade factors affecting its continued
existence, to the extent that listing
under the Act as an endangered or
threatened species is warranted at this
time.
Finding
As required by the Act, we considered
the five factors in assessing whether the
white-tailed prairie dog is endangered
or threatened throughout all of its range.
We have carefully examined the best
scientific and commercial information
available regarding the past, present,
and future threats faced by the whitetailed prairie dog. We reviewed the
petition, information available in our
files, and other available published and
unpublished information, and we
consulted with recognized white-tailed
prairie dog experts and other Federal,
State, and tribal agencies.
In considering what factors might
constitute threats, we must look beyond
the mere exposure of the species to the
factor to determine whether the species
responds to the factor in a way that
causes actual impacts to the species. If
there is exposure to a factor, but no
response, or only a positive response,
that factor is not a threat. If there is
exposure and the species responds
negatively, the factor may be a threat
and we then attempt to determine how
significant a threat it is. If the threat is
significant, it may drive or contribute to
the risk of extinction of the species such
that the species warrants listing as
endangered or threatened as those terms
are defined by the Act. This does not
necessarily require empirical proof of a
threat. The combination of exposure and
some corroborating evidence of how the
species is likely impacted could suffice.
The mere identification of factors that
could impact a species negatively is not
sufficient to compel a finding that
listing is appropriate; we require
evidence that these factors are operative
threats that act on the species to the
point that the species meets the
definition of endangered or threatened
under the Act.
We identified and evaluated the risks
of the present or threatened destruction,
modification, or curtailment of the
habitat or range of the white-tailed
prairie dog: (1) Oil and gas exploration
and development; (2) oil shale, tar
sands, and other minerals, (3) renewable
energy development—wind and solar;
(4) urbanization; (5) agricultural land
conversion; (6) grazing; (7) fire
occurrence and suppression; (8)
invasive plant species; and (9) climate
change. While oil and gas development
is impacting the species, we have no
evidence that it will significantly
threaten the species in the foreseeable
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future. We concluded that oil shale, tar
sands, and other minerals; renewable
energy development; urbanization;
agricultural land conversion; grazing;
fire suppression; invasive plant species;
and climate change are not significant
threats to the species now or in the
foreseeable future. Based on our review
of the best available information, we
find that the present or threatened
destruction, modification, or
curtailment of the white-tailed prairie
dog habitat or range is not a significant
threat now or in the foreseeable future.
We identified and evaluated the risks
from overutilization for commercial,
recreational, scientific, or educational
purposes. While shooting results in
some individual mortality and may
affect easily accessible colonies,
available evidence does not indicate
that the magnitude or intensity is
enough to significantly threaten the
species rangewide. Therefore, we
conclude that the white-tailed prairie
dog is not significantly threatened by
overutilization for commercial,
recreational, scientific, or educational
purposes now or in the foreseeable
future.
We found that plague impacts
populations throughout the species’
range. We determined that colonies and
complexes persist in the post-plague
environment, which demonstrates a
rangewide resiliency to the disease. We
determined that the species’ life-history
characteristics provide some protection
from the spread of plague and that
epizootic plague only affects a small
portion of the range at one time. The
threat of plague may decrease across the
range with the impacts of management
and climate change. Tularemia,
monkey-pox, and West Nile virus are
not considered threats to the species.
Additionally, we note that while whitetailed prairie dogs are prey for
numerous species, available information
does not indicate that predation has an
overall adverse effect on the species.
Therefore, we find that neither disease
nor predation is a significant threat to
the species now or in the foreseeable
future.
Based on our analysis of the existing
regulatory mechanisms, we determined
the States are actively involved in
managing the species through
conservation agreements and strategies.
Although these agreements are not
regulatory, they provide an important
mechanism for conservation,
monitoring, and research efforts. The
existing regulatory mechanisms in place
on State and Federal lands are limited.
However, we determined in the
evaluation that other threats would not
adversely affect the white-tailed prairie
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dog now or within the foreseeable
future. Additionally, the white-tailed
prairie dog receives some protection
from shooting under State laws in
Colorado and Utah, and from oil and gas
development in Utah. Therefore, based
on our review of the best available
scientific information, we conclude that
inadequacy of existing regulatory
mechanisms is not a significant threat to
the species now or in the foreseeable
future.
We also assessed the potential risks to
white-tailed prairie dogs from poisoning
and interspecific competition, and we
find that there is no evidence that
indicates these factors significantly
threaten the continued existence of
white-tailed prairie dog now or in the
foreseeable future.
We determined that energy
development, urbanization, grazing, fire
suppression, agricultural conversion,
recreational shooting, poisoning,
invasive plant species, and plague may
impact the species in at least localized
areas. White-tailed prairie dogs were
impacted throughout history by each of
these factors. We believe that,
collectively, these activities have
resulted in the presumed reduced
abundance of white-tailed prairie dog
from historical levels. We also believe
that the ecological function of this
species within western landscapes has
been altered from its historical function.
Many of these factors (grazing,
urbanization, fire suppression,
agricultural land use conversion, and
poisoning) were at much greater
magnitude in the past and are not
currently impacting species with the
same intensity. Other threats (oil and
gas development, climate change,
shooting, plague, and invasive plant
species) can be expected to continue
into the future. Of these, we consider
plague and oil and gas development to
have the greatest potential for
cumulative impacts. Yet some of the
most robust and resilient colonies exist
in areas where both of these potential
threats occur. Therefore, we do not
believe these factors will cumulatively
threaten the continued existence of
white-tailed prairie dog now or in the
foreseeable future.
Our review of the information
pertaining to the five threat factors does
not support a conclusion that there are
independent or cumulative threats of
sufficient imminence, intensity, or
magnitude that would cause substantial
losses of population distribution or
viability of the white-tailed prairie dog
that would result in the species being at
risk of extinction. Therefore, we do not
find that the white-tailed prairie dog is
currently in danger of extinction
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(endangered), nor do we find it is likely
to become endangered within the
foreseeable future (threatened),
throughout its range. Therefore, listing
the species as endangered or threatened
under the Act is not warranted at this
time.
Distinct Vertebrate Population
Segments
After assessing whether the species is
endangered or threatened throughout its
range, we next consider whether any
distinct vertebrate population segment
(DPS) exists and meets the definition of
endangered or is likely to become
endangered in the foreseeable future
(threatened).
Under the Service’s Policy Regarding
the Recognition of Distinct Vertebrate
Population Segments Under the
Endangered Species Act (61 FR 4722,
February 7, 1996), three elements are
considered in the decision concerning
the establishment and classification of a
possible DPS. These are applied
similarly for additions to or removal
from the Federal List of Endangered and
Threatened Wildlife. These elements
include:
(1) The discreteness of a population in
relation to the remainder of the taxon to
which it belongs;
(2) The significance of the population
segment to the taxon to which it
belongs; and
(3) The population segment’s
conservation status in relation to the
Act’s standards for listing, delisting
(removal from the list), or
reclassification (i.e., is the population
segment endangered or threatened).
Discreteness
Under the DPS policy, a population
segment of a vertebrate taxon may be
considered discrete if it satisfies either
one of the following conditions:
(1) It is markedly separated from other
populations of the same taxon as a
consequence of physical, physiological,
ecological, or behavioral factors.
Quantitative measures of genetic or
morphological discontinuity may
provide evidence of this separation.
(2) It is delimited by international
governmental boundaries within which
differences in control of exploitation,
management of habitat, conservation
status, or regulatory mechanisms exist
that are significant in light of section
4(a)(1)(D) of the Act.
The predicted range of the whitetailed prairie dog encompasses
13,066,887 ha (32,288,981 ac) (Seglund
et al. 2006, p. 91). We do not consider
any population segment of white-tailed
prairie dog to be markedly separated
from other populations of the same
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taxon as a consequence of physical,
physiological, ecological, or behavioral
factors. As a colonial species, whitetailed prairie dogs are naturally
distributed across the landscape in a
discontinuous fashion. Occupied habitat
changes rapidly, shifting on a landscape
scale (Seglund et al. 2006, p. iii). The
species spans Colorado, Utah,
Wyoming, and Montana. Available
information suggests while population
areas within Colorado and Utah are not
continuous with other populations areas
within the same State, they are
continuous between these States and
with populations in Wyoming.
Therefore, we do not consider any of
these areas to be physically discrete.
Because discontinuous distribution is
the ‘‘baseline’’ condition for the species,
for us to consider any geographic
discontinuity as being evidence of
marked separation (i.e., discreteness)
under the DPS policy, we would need
the best available information to
indicate that the amount of
discontinuity is over and above what is
considered to be normal for the species.
We do not have detailed mapping of
occupied habitat throughout the range
of the species. We recognize the likely
occurrence of some small, isolated
white-tailed prairie dog colonies, but
have very limited information available
that identifies their locations. Therefore,
we looked for other measures of
discontinuity, such as measures of
genetic or morphological differences as
guided by the DPS policy, to determine
whether any populations showed
evidence of marked separation. The
information available does not indicate
that any ecological or physical factors
have produced population segments
that express any genetic or
morphological discontinuity due to
separation from other prairie dog
populations. Gene flow via dispersal
and migration may maintain genetic
diversity in prairie dog species or help
restore genetic diversity in prairie dog
populations following plague epizootics
(Trudeau et al. 2004, p. 206). The
available information does not suggest
that populations differ genetically or
morphologically.
We determine, based on a review of
the best available information, that no
population segment of the white-tailed
prairie dog meets the discreteness
conditions of the 1996 DPS policy.
Therefore, no population segment
qualifies as a DPS under our policy and
is not a listable entity under the Act.
The DPS policy is clear that
significance is analyzed only when a
population segment has been identified
as discrete. Since we found that no
population segment met the
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discreteness element and, therefore, no
population segments qualify as a DPS
under the Service’s DPS policy, we will
not conduct an evaluation of
significance.
Significant Portion of the Range
Analysis
We evaluated the white-tailed prairie
dog’s predicted range in the context of
whether any potential threats are
concentrated in one or more areas of the
projected range, such that if there were
concentrated impacts, those white-tailed
prairie dog populations might be
threatened, and further, whether any
such population or complex might
constitute a significant portion of the
range. The potential threat factors we
evaluated for possible geographic
concentration were the most substantial
factor(s) affecting the species (in this
case, plague and habitat fragmentation
due to oil and gas development).
erowe on DSK5CLS3C1PROD with PROPOSALS-1
Plague
We regard sylvatic plague as the most
substantial factor affecting the whitetailed prairie dog. The disease is present
throughout the species’ range. We
consider the entire range of the species
to be operating in a post-plague
environment. We documented variation
between colonies and complexes in
their ability to maintain observed peaks
of abundance. However, this variation
occurred in every portion of the range,
and was not concentrated in any
geographic location. At this time, there
is no evidence to suggest that plague
affects portions of the range differently,
or will in the foreseeable future.
VerDate Mar<15>2010
17:00 May 28, 2010
Jkt 220001
Oil and Gas Development
Oil and gas development is a
widespread land use within the species’
range. Our analysis indicated a
concentration of oil and gas activity in
Uintah County, Utah, and the Northwest
IPA, located in adjacent Moffat, Mesa,
and Rio Blanco Counties in Colorado. A
similar concentration can be visually
observed in Sweetwater County,
Wyoming (Hotze 2010, p. 11). However,
some of the most robust and resilient
colonies are found within these areas of
concentrated development. The
available evidence does not indicate
that oil and gas development activities
are negatively impacting the species (see
Factor A. Oil and Gas Exploration and
Development). Given these factors, we
do not believe the regional
concentration of oil and gas
development is threatening the species
in these portions of its range.
On the basis of this review, we have
determined that the magnitude and
imminence of threats do not indicate
that the white-tailed prairie dog is in
danger of extinction, or likely to become
endangered, throughout all or a
significant portion of its range, within
the foreseeable future. The species also
does not meet the elements of our 1996
DPS Policy that would result in a DPS
designation for any segment of the
population. We conclude that no
Significant Portion of the Range (SPR)
exists for the white-tailed prairie dog.
We do not find that the species is in
danger of extinction now, nor is it likely
to become endangered within the
foreseeable future, throughout all or a
PO 00000
Frm 00061
Fmt 4702
Sfmt 9990
30363
significant portion of its range.
Therefore, listing the white-tailed
prairie dog as endangered or threatened
under the Act is not warranted at this
time.
We request that you submit any new
information concerning the status of, or
threats to, the white-tailed prairie dog to
our Utah Fish and Wildlife Office (see
ADDRESSES) whenever it becomes
available. New information will help us
monitor the white-tailed prairie dog and
encourage its conservation. If an
emergency situation develops for the
white-tailed prairie dog or any other
species, we will act to provide
immediate protection.
References Cited
A complete list of references cited is
available on the Internet at https://
www.regulations.gov and upon request
from the Utah Field Office (see
ADDRESSES).
Authors
The primary authors of this document
are the staff members of the Utah Field
Office, West Valley City, Utah.
Authority
The authority for this section is
section 4 of the Endangered Species Act
of 1973, as amended (16 U.S.C. 1531 et
seq.).
Dated: May 14, 2010
Daniel M. Ashe,
Acting Director, Fish and Wildlife Service.
[FR Doc. 2010–12599 Filed 5–28–10; 8:45 am]
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Agencies
[Federal Register Volume 75, Number 104 (Tuesday, June 1, 2010)]
[Proposed Rules]
[Pages 30338-30363]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2010-12599]
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DEPARTMENT OF THE INTERIOR
Fish and Wildlife Service
50 CFR Part 17
[Docket No. FWS-R6-ES-2008-0053]
[MO 92210-0-0008-B2]
Endangered and Threatened Wildlife and Plants; 12-month Finding
on a Petition to List the White-tailed Prairie Dog as Endangered or
Threatened
AGENCY: Fish and Wildlife Service, Interior.
ACTION: Notice of a 12-month petition finding.
-----------------------------------------------------------------------
SUMMARY: We, the U.S. Fish and Wildlife Service announce a 12-month
finding on a petition to list the white-tailed prairie dog (Cynomys
leucurus) as endangered or threatened under the Endangered Species Act
of 1973, as amended. After a review of all available scientific and
commercial information, we find that listing the white-tailed prairie
dog is not warranted at this time. However, we ask the public to submit
to us any new information that becomes available concerning the threats
to the white-tailed prairie dog or its habitat at any time.
DATES: The finding announced in this document was made on June 1, 2010.
ADDRESSES: This finding is available on the Internet at https://www.regulations.gov at Docket Number FWS-R6-ES-2008-0053. Supporting
documentation we used in preparing this finding is available for public
inspection, by appointment, during normal business hours at the U.S.
Fish and Wildlife Service, Utah Field Office, 2369 West Orton Circle,
Suite 50, West Valley City, UT 84119. Please submit any new
information, materials, comments, or questions concerning this finding
to the above street address.
FOR FURTHER INFORMATION CONTACT: Larry Crist, Field Supervisor, Utah
Field Office (see ADDRESSES); by telephone at 801-975-3330; or by
facsimile at 801-975-3331. If you use a telecommunications device for
the deaf (TDD), please call the Federal Information Relay Service
(FIRS) at 800-877-8339.
SUPPLEMENTARY INFORMATION:
Background
Section 4(b)(3)(B) of the Endangered Species Act of 1973, as
amended (Act) (16 U.S.C. 1531 et seq.), requires that, for any petition
to revise the Federal Lists of Endangered and Threatened Wildlife and
Plants that contains substantial scientific or commercial information
that listing the species may be warranted, we make a finding within 12
months of the date of receipt of the petition. In this finding, we will
determine that the petitioned action is: (1) Not warranted, (2)
warranted, or (3) warranted, but the immediate proposal of a regulation
implementing the petitioned action is precluded by other pending
proposals to determine whether species are endangered or threatened,
and expeditious progress is being made to add or remove qualified
species from the Federal Lists of Endangered and Threatened Wildlife
and Plants. Section 4(b)(3)(C) of the Act requires that we treat a
petition for which the requested action is found to be warranted but
precluded as though resubmitted on the date of such finding, that is,
requiring a subsequent finding to be made within 12 months. We must
publish these 12-month findings in the Federal Register.
Previous Federal Action
On July 15, 2002, we received a petition dated July 11, 2002, from
the Center for Native Ecosystems, Forest Guardians, Biodiversity
Conservation Alliance, and Terry Tempest Williams, requesting that the
white-tailed prairie dog (Cynomys leucurus) be listed as endangered or
threatened across its entire range. We acknowledged the receipt of the
petition in a letter to the petitioners, dated August 27, 2002. In that
letter we also stated that higher priority actions precluded addressing
the petition immediately, but it would be addressed when funding
allowed.
Section 4(b)(3)(B) of the Act requires that for any petition to
revise the Lists of Threatened and Endangered Wildlife and Plants, to
the maximum extent practicable, within 90 days after receiving the
petition, we make a finding as to whether the petition presents
substantial scientific or commercial information indicating that the
petitioned action may be warranted. On November 9, 2004, we announced
our 90-day finding (69 FR 64889) that the petition did not present
substantial scientific or commercial information indicating that
listing may be warranted. On July 12, 2007, in a Director's memorandum,
the U.S. Fish and Wildlife Service (Service) announced that we would
review the November 9, 2004, finding after questions were raised about
the integrity of scientific information used and whether the decision
was consistent with the appropriate legal standards. We received notice
of a lawsuit from the Center for Native Ecosystems, and three other
entities, on November 27, 2007, regarding our not-substantial 90-day
finding. We agreed in a stipulated
[[Page 30339]]
settlement agreement on February 22, 2008, to submit a notice
initiating a 12-month finding for the white-tailed prairie dog to the
Federal Register on or before May 1, 2008, and to submit a 12-month
finding for the white-tailed prairie dog to the Federal Register on or
before June 1, 2010. Due to the stipulated settlement agreement, the
petitioners dismissed the lawsuit on February 26, 2008. This notice
constitutes the 12-month finding under the stipulated settlement
agreement on the petition to list the white-tailed prairie dog as
endangered or threatened.
Species Information
Species Description
White-tailed prairie dogs are between 340 to 370 millimeters (mm)
(13.4 to 14.6 inches (in)) in length with a 40- to 65-mm (1.6- to 2.6-
in) long tail (Clark et al. 1971, p. 1). The tail has a grayish white
tip and is white on the terminal half. The coat is generally yellow-tan
with distinctive dark brown or black cheek patches that extend above
the eye with a lighter black stripe that extends below the eye onto the
cheek (Clark et al. 1971, p. 1).
Taxonomy
The white-tailed prairie dog is one of five prairie dog species
that inhabit western North America (Clark et al. 1971, p. 1; Pizzimenti
1975, pp. 62-63). Prairie dogs are in the squirrel family, Sciuridae,
and belong to the genus Cynomys (Hollister 1916, p. 5). The genus is
split into two subgenera; Leucocrossuromys includes prairie dogs with
white tails and Cynomys includes prairie dogs with black tails. White-
tailed prairie dogs are included in the subgenus Leucocrossuromys along
with Utah and Gunnison prairie dogs (Clark et al. 1971, p. 1;
Pizzimenti 1975, pp. 15-16). Due to this consensus, we determined that
the white-tailed prairie dog is a valid taxonomic species and a
listable entity under the Act.
Ecology and Life History
White-tailed prairie dogs occur at elevations ranging from 1,150
meters (m) (3,773 feet (ft)) (Flath 1979, p. 63) to 3,200 m (10,500 ft)
(Tileston and Lechleitner 1966, p. 295). Unlike the grass-dominated
habitats of black-tailed prairie dogs, white-tailed prairie dogs
inhabit drier landscapes with shrubland vegetation (Tileston and
Lechleitner 1966, p. 295; Clark 1977, pp. 3-5; Collins and Lichvar
1986, pp. 88-91; Gadd 2000, pp. 15-16). Their habitats are generally
flat (Collins and Lichvar 1986, p. 92).
Prairie dogs are primarily herbivorous and mainly eat grasses and
forbs (Kelso 1939, pp. 7-11). However, they consume other plants
seasonally. Prairie dog selection of plants is somewhat dependent on
site-specific conditions and seasonality. For example, white-tailed
prairie dogs eat sagebrush and saltbush during early spring, grasses in
the summer, and seed heads and rabbitbrush flowers in the fall (Kelso
1939, p. 10; Tileston and Lechleitner 1966, p. 302). White-tailed
prairie dogs eat the least amount of grass of any prairie dog species
and the most saltbush (Kelso 1939, p. 11). White-tailed prairie dogs
also eat insects (Stockard 1929, p. 476). Prairie dogs obtain most of
their water by eating vegetation and can become water-stressed if
sufficient succulent vegetation is unavailable (Seglund et al. 2006, p.
7).
White-tailed prairie dogs prefer areas with lower vegetation
heights (Collins and Lichvar 1986, p. 92), but they may use dense
sagebrush adjacent to grassier areas (Tileston and Lechleitner 1966, p.
314). White-tailed prairie dogs use the dense vegetation within
sagebrush habitat to hide from predators (Hoogland 1981, pp. 266-268;
Gadd 2000, pp. 24-26), reducing their need to visually search for
predators and consequently reducing their need for dense colonies and
cohesive social structures. This habitat use differs from black-tailed
prairie dogs, who actively work to maintain the grassland vegetation
surrounding their burrows for visibility.
White-tailed prairie dogs dig their own burrows. Burrow
construction requires deep, well-drained soils. Preferred soils are
derived from sandstone or shale and may be clay-loam, silty clay, or
sandy loam (Lupis et al. 2007, p. 6). Burrows are used throughout the
year for hibernation, cover from temperature extremes, predator
avoidance, and birthing and raising young (Clark 1977, p. 9; Hoogland
1981, pp. 258-264). Burrow complexes are usually widespread with
numerous entrances, tunnels, and chambers. The number of burrows in an
area varies greatly from location to location, ranging from 0.12 to
47.75 per hectare (ha) (0.3 to 118 per acre (ac)) with a mean of 0.32
to 6.79 per ha (0.8 to 16.8 per ac) (Tileston and Lechleitner 1966, p.
314; Menkens and Anderson 1989, p. 84; Seglund and Schnurr 2009, p.
94).
For purposes of this finding, a group of burrows is referred to as
a colony. A complex is a collection of colonies grouped on the
landscape. There is usually a high degree of connectivity between
colonies in the same complex.
White-tailed prairie dog colonies have fewer animals per unit area
with less obvious borders than black-tailed prairie dog colonies
(Tileston and Lechleitner 1966, pp. 297, 314; Hoogland 1981, p. 252).
Home range sizes range from 0.2 to 1.9 ha (0.5 to 4.7 ac) (Clark 1977,
p. 65; Cooke 1993, p. 23), which are generally larger than black-tailed
prairie dog home ranges (Clark 1977, p. 65).
White-tailed prairie dogs can live up to 8 years in captivity but
may not live past 4 years in the wild (Pauli et al. 2006, p. 18).
Prairie dog annual mortality rates average 30 to 60 percent, largely
due to disease and predation (Tileston and Lechleitner 1966, p. 305;
Clark 1977, pp. 80-81).
Adult sex ratios are approximately one male to two females (Clark
1977, p. 76; Hoogland 2010, pers. comm.). White-tailed prairie dogs can
reproduce at 1 year of age, and they have a single litter once a year
averaging four to five pups (Bakko and Brown 1967, pp. 110-111).
Breeding occurs from late March to mid-April (Tileston and Lechleitner
1966, p. 303). Pups are born in the burrows after a gestation period of
approximately 30 days (Tileston and Lechleitner 1966, p. 304), and
emerge from the burrow for the first time 4 to 6 weeks after birth
(Bakko and Brown 1967, p. 103). They begin to disperse from the colony
in June and July when population densities are the highest (Clark 1977,
p. 72). Migration is recognized as an important factor to white-tailed
prairie dog population dynamics (Clark 1977, p. 80). Plague in this
species often results in near extirpation of colonies. Rapid
recolonization of some areas post-plague with few or no surviving
reproductive adults suggests the species is highly mobile (Seglund et
al. 2006, p. 10). Dispersal distances of up to 8 kilometers (km) (4.8
miles (mi)) have been observed (Cooke 1993 in Seglund et al. 2006, p.
10)
White-tailed prairie dogs have the least cohesive social structure
of any prairie dog species. Their social system is organized around
family groups or ``clans,'' comprised of several reproductive females,
one or two males of reproductive age, and dependent young (Clark 1977,
p. 62; Cooke 1993, p. 22). Adult white-tailed prairie dogs spend little
time displaying social behavior, and most of their time feeding or in
alert postures (Clark 1977, p. 44). Pups spend a large amount of time
playing during their first few weeks (Tileston and Lechleitner 1966, p.
300).
White-tailed prairie dog populations exhibit large fluctuations of
more than
[[Page 30340]]
50 percent from year to year (Menkens and Anderson 1989, p. 345).
Population fluctuations are likely due to disease cycles, vegetation
quantity and quality, and drought (Seglund and Schnurr 2009, p. 16)
(see Factor A. Climate Change; Factor C. Disease). We do not know the
level at which population fluctuations are a natural part of white-
tailed prairie dog ecology, or the result of environmental or human-
caused threat factors. In many cases, prairie dog colonies persist
despite large population fluctuations (see Factor C. Disease). We
define ``persistence'' as the long-term continuance of white-tailed
prairie dog colonies, at a high enough level to exist in the long-term
with minimal management assistance.
White-tailed prairie dogs are diurnal (active during the day)
(Tileston and Lechleitner 1966, p. 200). They are active approximately
5 to 7 months per year from early spring to fall and hibernate during
late fall and winter (Clark 1977, pp. 59-60; Cooke 1993, p. 11). Time
spent hibernating is determined by available food resources (Clark
1977, p. 60). In warm weather, even in mid-winter, white-tailed prairie
dogs will feed if grasses are growing (Hollister 1916, p. 6; Goodrich
and Buskirk 1998, p. 177). If resources are not sufficient, prairie
dogs become inactive and spend more time in their burrows (Harlow and
Menkens 1986, p. 795). During periods of high summer temperatures,
white-tailed prairie dogs avoid the highest temperatures of midday by
foraging in the cooler morning and evening hours (Clark 1977, p. 58).
Distribution and Abundance
The overall species' distribution is mapped as ``gross range.'' The
available white-tailed prairie dog literature uses the term ``gross
range'' to describe the outer boundary identifying the overall
rangewide distribution of the white-tailed prairie dog (Figure 1).
However, not all lands within the species' gross range are occupied or
have the potential to be occupied by white-tailed prairie dogs (Seglund
et al. 2006, p. 100). The predicted range is a subset of the gross
range and thus represents a more accurate spatial representation of the
potential range of the white-tailed prairie dog (Seglund et al. 2006,
pp. 16, 110; Seglund and Schnurr 2009, p. 23). Predicted range is
defined using habitat characteristics of vegetation, land use, slope,
and elevation (Seglund et al. 2006, pp. 14-39). Depending on available
data, we use gross range, predicted range, or mapped occupied habitat
throughout this document to evaluate status and threats to the species.
For example, gross range mapping data was available for our use for all
States across the species' range. However, the data for the predicted
range map (Seglund et al. 2006, p. 110; Seglund and Schnurr 2009, p.
23) was only available for the State of Colorado. Information regarding
mapped occupied habitat (all areas mapped on Federal lands as occupied
by white-tailed prairie dogs since 1985) was available for the State of
Utah, but not for any other States.
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The white-tailed prairie dog occurs from a small area in south-
central Montana, throughout much of Wyoming, into western Colorado, and
northeastern Utah. There are 20,224,801 ha (49,976,572 ac) within the
gross range of the white-tailed prairie dog and 13,066,887 ha
(32,288,981 ac) within the species' predicted range (Seglund et al.
2006, p. 91). Therefore, approximately 65 percent of the gross range
has the characteristics necessary to support the white-tailed prairie
dog. Wyoming contains the largest amount of white-tailed prairie dog
predicted range (75 percent) (Knowles 2002, p. 4). Less than 1 percent
of predicted range occurs in Montana (Table 1). The majority of white-
tailed prairie dog predicted range (56 percent) occurs on land managed
by the Bureau of Land Management (BLM). A significant portion of the
predicted range occurs on private land (37 percent). Very little of the
predicted range is managed by the Service (0.4 percent), U.S. Forest
Service (USFS) (0.5 percent), or National Park Service (NPS) (0.9
percent) (Table 1).
TABLE 1. Percent Predicted Range by State and Land Management Entity (Seglund et al. 2006, pp. 91, 98, 100, 104, 109).
--------------------------------------------------------------------------------------------------------------------------------------------------------
Total Range Private BLM USFS NPS USFWS State Other
--------------------------------------------------------------------------------------------------------------------------------------------------------
Colorado 11 37 56 < 1 1 < 1 5 < 1
--------------------------------------------------------------------------------------------------------------------------------------------------------
Montana < \*\ 1 49 44 2 0 0 5 < 1
--------------------------------------------------------------------------------------------------------------------------------------------------------
Utah 13 20 60 < 1 < 1 < 1 11 7
--------------------------------------------------------------------------------------------------------------------------------------------------------
Wyoming 75 33 54 < 1 < 1 < 1 6 6
--------------------------------------------------------------------------------------------------------------------------------------------------------
Total 37 56 < 1 < 1 < 1 5 < 1
--------------------------------------------------------------------------------------------------------------------------------------------------------
* < less than
Historical abundance and distribution are not well documented for
white-tailed prairie dogs prior to the 1980s (Pauli et al. 2006, p. 13;
Seglund et al. 2006, p. 11). The distribution of white-tailed prairie
dogs has not changed appreciably since historic times (Knowles 2002,
pp. 5-6). The only recorded change in distribution is in Montana, where
white-tailed prairie dogs were previously captured 40 miles north of
currently occupied habitat (Knowles 2002, p. 5). However, abundance
declined as a result of past control efforts and plague (Cully 1993, p.
38; Knowles 2002, pp. 1-2) (see Factor B. Overutilization and Factor C.
Disease). We are not able to quantify changes in occupied habitat for
the species because mapping did not use standardized methods, and we do
not have accurate estimates of historical occupied habitat (Seglund et
al. 2006, p. 13).
We do not have rangewide population trend information due to a lack
of historical population information and inconsistencies in survey
methodologies (Seglund et al. 2006, pp. 4, 13). Surveys for white-
tailed prairie dog distribution and occupancy rates were recently
conducted across portions of the species' gross range (Grenier and
Filipi 2009, entire; Seglund and Schnurr 2009, p. 27; Wright 2009,
entire). While occupancy surveys are intended to determine population
trends (Seglund and Schnurr 2009, p. 10), the data are not yet
available to provide trend information. In addition, each State used
different methods to conduct ground surveys and determine occupancy
rates; thus, the results are not comparable. We present State-by-State
information below with the caveat that comparing colony occupancy rates
across the gross range of the species is not possible.
Colorado
White-tailed prairie dog predicted range includes Moffat, Routt,
Rio Blanco, Garfield, Mesa, Delta, Montrose, Eagle, Jackson, Ouray, and
Larimer Counties in northwestern Colorado (Seglund et al. 2004, p.
133). Approximately 1,246,441 ha (3,104,733 ac) of predicted white-
tailed prairie dog habitat occurs in three Individual Population Areas
(IPAs): Grand Valley-Uncompahgre IPA, North IPA, and Northwest IPA
(Hotze 2010, pp. 9-10). An IPA is an area physically separated from
other populations that may face a unique subset of threats (Seglund and
Schnurr 2009, p. 1). These population areas are geographically
separated from each other but connected to population areas in Utah and
Wyoming (Seglund and Schnurr 2009, p. E-5).
Colorado completed Statewide white-tailed prairie dog surveys in
2004 and 2008; occupancy rates were 24.1 and 23.1 percent,
respectively, a statistically insignificant difference (Seglund and
Schnurr 2009, pp. 27-28). Occupancy rate is the number of randomly
selected plots in predicted habitat with prairie dogs, and is not a
measure of abundance. We do not have population trend information
across the entire predicted range of the species in Colorado. Localized
declines and habitat degradation were reported in the Grand Valley-
Uncompahgre IPA due largely to urbanization (Seglund and Schnurr 2009,
p. 54). Information in the North IPA is restricted to colonies
associated with black-footed ferret reintroduction; a historical record
of ferrets in this area suggests it once supported abundant populations
of prairie dogs (Seglund and Schnurr 2009, p. 58). Only two colonies
remain, although they have remained stable for the past 20 years
(Seglund and Schnurr 2009, p. 58). Population densities and
distribution in the Northwest IPA appear to fluctuate greatly in large
part due to the prevalence of plague (Seglund and Schnurr 2009, pp. 63-
76).
Montana
White-tailed prairie dogs occur in one population area in Carbon
County, along the Montana-Wyoming border (Seglund et al. 2006, p. 25).
Fifteen colonies were mapped in the 1970s across 312.8 ha (773 ac)
(Flath 1979, p. 63). White-tailed prairie dogs were previously reported
in north Sage Creek in Carbon County (Hollister 1916, p. 27), and in
Yellowstone County just northeast of Carbon County (Kelso 1939, p. 7),
but no animals were found in these locations in later surveys (Flath
1979, entire).
Current occupied area of white-tailed prairie dogs in Montana
includes 112 ha (277 ac) across 11 colonies; 8 colonies were considered
active in 2009 (MFWP 2009a, p. 1). The apparent loss in occupied
habitat is likely due to plague and agricultural land conversion (Parks
et al. 1999 in Knowles 2002, p. 15). We do not have population trend
data for the white-tailed prairie dog in Montana.
[[Page 30343]]
Utah
White-tailed prairie dogs occur in Rich, Summit, Daggett, Uintah,
Duchesne, Carbon, Emery, and Grand Counties (Seglund et al. 2004, p.
140) in northern and eastern Utah. In 2002 and 2003, 57,463 ha (141,808
ac) of occupied white-tailed prairie dog habitat were documented,
mostly within Uintah and Duchesne Counties (Lupis et al. 2007, p. 17).
Smaller population areas are found in the Cisco Desert in Emery and
Grand Counties (10,869 ha (26,856 ac)), and in Rich County (73 ha (180
ac)) (Lupis et al. 2007, p. 15). Surveys did not include private lands;
therefore, the amount of occupied habitat is an underestimate. These
population areas are mostly disconnected from each other, but connect
to population areas in Wyoming and Colorado. Based on surveys conducted
in 2008, the white-tailed prairie dog occupancy rate was 46 percent of
sampled plots (Wright 2009, p. 5).
We do not have information on long-term population status or trends
for white-tailed prairie dogs in Utah. Surveys in black-footed ferret
management areas in the Uintah basin recorded fluctuating population
levels: increasing densities since the early 1990s, declines in 1999
and 2003, and population recoveries in 2004-2008 (Seglund et al. 2006,
p. 28; Maxfield 2009, pers. comm.) (see Factor A. Climate Change).
Wyoming
White-tailed prairie dogs are found in the Counties of Big Horn,
Park, Hot Springs, Natrona, Fremont, Sublette, Sweetwater, Lincoln,
Uinta, Carbon, and Albany in northern and southern central Wyoming
(Seglund et al. 2004, p. 130). Wyoming Fish and Game documented
11,511,356 ha (27,822,847 ac) of potential habitat and 1,170,952 ha
(2,893,487 ac) of occupied habitat in 2008 by aerial survey (Grenier
and Filipi 2009, p. 5). The majority of these acres are in Albany and
Carbon Counties. Habitat in Wyoming is mostly continuous and not split
into discrete population areas. Approximately 68 percent of the
surveyed areas were estimated to be occupied (Grenier and Filipi 2009,
p. 5). This estimate is not a statistically determined ``occupancy
rate.'' Occupancy from these aerial surveys cannot be compared with
ground surveys from Colorado and Utah, because the observed location of
colony boundaries varies between methods, presumably due to the
difficulty in measuring colony boundaries from the air (Andelt et al.
2005, p. 3). We do not have long-term status or trend information for
white-tailed prairie dogs in Wyoming.
Summary of White-Tailed Prairie Dog Population Status
We do not have reliable long-term historical or current white-
tailed prairie dog status, trend, or distribution data. White-tailed
prairie dog populations are likely below historical levels, though
their overall distribution has not substantially changed (Knowles 2002,
p. 6). Large acreages of occupied habitat exist across the species'
range, particularly in Wyoming. Each State plans to continue occupancy
surveying, so more information may be available in the future.
Evaluation of Information Pertaining to the Five Threat Factors
Section 4 of the Act and implementing regulations (50 CFR 424) set
forth procedures for adding species to, removing species from, or
reclassifying species on the Federal Lists of Endangered and Threatened
Wildlife and Plants. Under section 4(a)(1) of the Act, a species may be
determined to be endangered or threatened based on any of the following
five factors:
(A) The present or threatened destruction, modification, or
curtailment of its habitat or range;
(B) Overutilization for commercial, recreational, scientific, or
educational purposes;
(C) Disease or predation;
(D) The inadequacy of existing regulatory mechanisms; or
(E) Other natural or manmade factors affecting its continued
existence.
In making this 12-month finding, information pertaining to the
white-tailed prairie dog in relation to the five factors provided in
section 4(a)(1) of the Act is discussed below. In making our 12-month
finding on the petition we considered and evaluated the best available
scientific and commercial information.
Factor A. The present or threatened destruction, modification, or
curtailment of the species' habitat or range.
The following potential factors that may affect the habitat or
range of the white-tailed prairie dog are discussed in this section,
including: (1) Oil and gas exploration and development, (2) oil shale
and tar sands development, (3) mineral development, (4) renewable
energy development--wind and solar, (5) urbanization, (6) agricultural
land conversion, (7) grazing, (8) fire occurrence and suppression, (9)
invasive plant species and (10) climate change.
Oil and Gas Exploration and Development
Exploration and development of oil and gas resources is widespread
throughout the gross range of the white-tailed prairie dog (Hotze 2010,
pp. 11-26). Between 2004 and 2008, exploration of oil and gas in the
intermountain west increased substantially because of political and
economic incentives (National Petroleum Council 2007, pp. 5-7). The
2005 Energy Policy Act expedited the leasing and permitting process on
Federal lands (42 U.S.C. 15801). The global recession of 2008 resulted
in decreased energy demand resulting in a reduced rate of energy
development. Fossil fuel production is expected to regain and surpass
the early 2008 levels in 2010-2030 (Copeland et al. 2009, p. 1; Energy
Information Administration (EIA) 2009, p. 109).
Energy development includes exploration, drilling, production, and
reclamation phases (Tribal Energy and Environmental Information
Clearinghouse (TEEIC) 2009, entire), each of which may potentially
impact the white-tailed prairie dog or its habitat. During the
exploration phase, oil and gas resources are delineated using a variety
of technologies, including seismic shot-hole surveys (planting and
detonation of underground explosives to produce vibrations that reveal
locations of mineral resources) and vibroseis trucks (vehicle with a
vibration plate used to survey mineral resources) (TEEIC 2009, p. 6).
These activities may result in mortality and the crushing of vegetation
along the seismic route, but there are no permanent structures
established during the exploration phase. If oil and gas resources are
proven, the lessee moves into the drilling phase. During the drilling
phase, access roads and well pads are constructed, pipelines are
installed, and the infrastructure necessary for the production phase
(such as compressor stations) is developed and constructed (TEEIC 2009,
p. 9). This phase typically results in longer-term disturbance to
white-tailed prairie dog habitat. The production phase includes
maintaining the wells and infrastructure as well as continuing the
extraction of the oil and gas resources. Wells may be in the production
phase for up to 20 to 30 years for gas wells (TEEIC 2009, p. 5) and up
to 100 years for oil wells (Connelly et al. 2004, p. 7:41). The final
phase begins when a well is no longer producing oil or gas because the
[[Page 30344]]
resource is depleted. The lessee is responsible for reclaiming the land
back to its original condition, or as close to the original condition
as possible (BLM 2007a, p. 2; TEEIC 2009, p. 15).
Oil and gas developments are typically configured as point (e.g.,
well pads, compressors) and line (e.g., roads, pipelines) disturbances
across broad areas. The amount of direct habitat loss may encompass 5
to 10 percent of leased areas. However, the extent of disturbance to
white-tailed prairie dogs may reach far beyond the direct habitat loss,
due to the loss and fragmentation of habitats; the alteration of
vegetation resources, which often promotes nonnative invasive plant
species; increased noise levels; increased vehicle traffic; and
increased human access to previously remote areas (Pauli et al. 2006,
p. 27; Seglund et al. 2006, p. 46; Seglund and Schnurr 2009, p. 126;
Wyoming Game and Fish Department (WGFD) 2009, p. 10). The amount of
direct habitat loss and total fragmentation varies greatly depending on
well density (number of acres per well) and spacing (distance between
individual well pads). Increasing wells per unit area decreases the
amount of habitat available for wildlife. Well densities and spacing
are typically designed to maximize recovery of the resource and are
administered by State oil and gas agencies and the BLM on Federal
mineral estate. Each geologic basin has a standard spacing, but
exemptions are granted (Connelly et al. 2004, pp. 7-39 to 7-40). Within
the range of the white-tailed prairie dog, well spacing can vary from 5
to 160 acres per well. Larger well spacing is often characterized by
more wells drilled per pad. Increasing the number of wells per pad
increases the size of the individual pad but decreases the amount of
habitat fragmented. The variation in well and well pad spacing results
in a variation in the intensity of effects across the species' range.
However, we are unable to determine how the ultimate effects to the
species vary with well density. The threshold levels of oil and gas
development that result in reduced populations or eliminated colonies
are unknown.
Resulting impacts to white-tailed prairie dogs from oil and gas
development may include direct mortality from vehicles; direct
mortality associated with increased access by recreational shooters who
utilize the new access routes (Gordon et al. 2003, p. 12); increased
disturbance responses from increased human activity; direct loss of
habitat and forage resources during exploration, drilling, and
production; and indirect loss of forage resources from invasive,
nonnative plant species (Seglund and Schnurr 2009, p. 126).
No studies have been done regarding the short-term or long-term
impact of oil and gas development on individual white-tailed prairie
dogs or their colonies. White-tailed prairie dogs can be negatively
impacted by the direct loss of habitat that occurs as a result of
development. For example, white-tailed prairie dog burrow densities
were lower at well locations compared to areas further from the well
pads (Biggins et al. 1984, p. 12). Dead prairie dogs were found in oil
and gas reserve pits (Esmoil 1995 in Peterson 2008, p. 5), although the
extent of population level impact is not known. The use of vibroseis
trucks in prairie dog colonies appears to impact vegetation, but
preliminary results did not document prairie dog mortality or burrow
collapse (Young and Sawyer 1981, pp. 1-2; Menkens and Anderson 1985, p.
7).
However, as described above, exposure to a factor does not
necessarily indicate that the factor is a threat. We know that white-
tailed prairie dog colonies exist in areas with long-term oil and gas
development. Some of the largest and most robust colonies are located
near areas of intense oil and gas development (see Distribition and
Abundance, above, and our discussion under Factor C, below). For
example, the Coyote Basin, Kennedy Wash, and Snake John colonies in
Uintah County, Utah, occur within a landscape fragmented by oil and gas
infrastructure, although their immediate occupied habitats have not
sustained significant energy development. Fifty percent of the mapped
occupied habitat in this region has been leased with 17 percent
currently producing (See Utah, below). Populations in this area have
fluctuated; although this has been attributed to drought (See Climate
Change, below). Despite the high amount of leasing in this area,
populations have recovered to their 20 year recorded peak. Similarly,
Coyote Basin and Wolf Creek are historically Colorado's most robust
colonies and occur within the Northwest IPA where oil and gas
development is high. Forty one percent of this IPA has already been
leased, with 7 percent currently producing (Hotze 2010, p. 20). Prairie
dogs continue to occupy a moderately sized complex within the Coal Oil
Basin (Colorado's largest oil field) despite an active drilling history
that extends back to 1944 (Wolf Creek Work Group 2001, p. 15).
Available information does not indicate that white-tailed prairie
dogs are currently reacting to oil and gas activities on a local
landscape scale or at the population or species level. We also do not
know if there is a level of oil and gas development at which the status
of prairie dogs at the population or species level would be negatively
impacted. As described above, white-tailed prairie dogs persist in
several areas with oil and gas activity.
To evaluate the extent to which oil and gas development may affect
white-tailed prairie dogs in the foreseeable future, we overlaid BLM-
authorized oil and gas leases with the species' gross range. More
specific information was available for Utah and Colorado, so we
overlaid oil and gas development with white-tailed prairie dog
predicted range (Seglund and Schnurr 2009, p. 24) in Colorado and
mapped occupied habitat in Utah (Hotze 2010, p. 7). We also reviewed
information on State-specific potential oil and gas reserves where that
information was available. The results are presented below and in the
State-by-State analysis sections.
In additional to managing lands in Wyoming, Colorado, and Utah, the
BLM manages the Federal mineral estate, including authorizing oil and
gas leases. Leases may be producing or non-producing. Producing leases
are those being actively developed. Non-producing leases are leased;
however, the resources for which they were leased are not currently
being extracted. Non-producing leases may become developed in the
future, but development is not guaranteed (Thompson 2010, pers. comm.).
We consider these leases to be indicative of potential development.
However, we do not know the percent of non-producing leases that will
become developed in the future because the variables governing
development are complex and include the price of gas, the number of
other leases the company holds, the actual amount of resource the lease
contains (often unknown at the time of lease), and other complex
economic and social factors.
In addition to the producing and non-producing leases, BLM has
authorized a significant amount of the Federal mineral estate that may
be leased in the future. Each BLM field office developed a resource
management plan that delineates areas available for leasing and depicts
surface access constraints (e.g., BLM 2008a, p. 7). The areas that are
available for leasing are larger than those that have already been
authorized, and include areas that may be developed in the future
should proven reserves be located. Development of the entire area
available for leasing is unlikely due to BLM's multi-use mandate, but
the area available for
[[Page 30345]]
leasing represents a potential maximum of oil and gas development. Non-
Federal mineral estates are managed by State, tribal, and private
mineral rights owners under different programs and using different
processes.
We were unable to specifically quantify the impacts of development
on non-Federal mineral rights. Total active and plugged wells are
available as GIS layers from each State's oil and gas development
commission. However, number of wells is not a biologically meaningful
measure to the white-tailed prairie dog because the effects depend on
the amount of land leased and well density and spacing. As previously
stated, the impacts to the species at different well spacing densities
are not well understood. Approximately two-thirds of wells within the
species range are located on Federal versus non-Federal estate (BLM
2009; Colorado Oil and Gas Conservation Commission 2010; Wyoming Oil
and Gas Conservation Commission 2010; Utah Division of Oil and Mining
2010; unpublished data). Similarly, approximately two-thirds of the
species range is in Federal vs. non-Federal ownership. We assume that a
similar ratio of development of non-Federal minerals is likely to occur
in the future as is occurring for Federal minerals. Because leasing
does not guarantee development, and the fact that we are unable to
estimate leasing rates on non-Federal estate, we consider the numbers
presented below (in the State-by-State analysis) as an approximate
measurement of Federal and non-Federal development that could occur in
the foreseeable future.
The BLM has authorized 5,687,259 ha (14,053,523 ac) of producing
and non-producing leases for oil and gas development, representing
approximately 28 percent of the white-tailed prairie dog's gross range
(Hotze 2010, p. 18). Producing leases occur across 1,435,580 ha
(3,547,395 ac), or 7 percent, of the species' gross range (Hotze 2010,
p. 18). Future exploration and development of fossil fuels is likely to
focus in areas of highest potential return. Highest potential return is
defined by several geological characteristics including permeability
and porosity of the underlying rock (BLM 2005a, p. 41). For example, in
the BLM Little Snake field office of northwest Colorado, approximately
96 percent of new wells will be drilled in areas with high oil and gas
potential (BLM 2007b, p. 3:100). In high and moderate potential areas
in Wyoming, a single well can produce 4 to 30 times as much as a well
in low potential areas (BLM 2008b, p. A20:6). Therefore, we assume
these areas will be the focus of future leasing.
Colorado
In Colorado, the BLM authorized oil and gas leases on 30 percent of
the white-tailed prairie dog's predicted range in the State (Hotze
2010, p. 20) across the Northwest, North, and Grand Valley-Uncompahgre
IPAs. Of the authorized oil and gas leases within the predicted range
in Colorado, there are 61,334 ha (151,560 ac) of producing leases,
which comprise approximately 5 percent of the predicted State range
(Hotze 2010, p. 14). Non-producing leases encompass 311,650 ha (770,104
ac), or approximately 25 percent of the predicted State range (Hotze
2010, p. 14).
Northwest Individual Population Area (IPA)
The Northwest IPA in Moffat and Rio Blanco Counties is within the
Greater Green River Basin (DOI et al. 2006, p. 20) and has the highest
potential for oil and gas development (Seglund and Schnurr 2009, p.
61). This IPA comprises approximately 54 percent of white-tailed
prairie dog predicted habitat in Colorado (Hotze 2010, p. 10).
Authorized lease areas in 2009 encompassed approximately 41 percent of
the Northwest IPA (Hotze 2010, p. 20), and oil and gas development is
projected to significantly increase over the next 20 years (Seglund and
Schnurr 2009, p. 128). For example, the BLM anticipates authorizing the
drilling of 3,031 oil and gas wells over the next 20 years in Routt and
southwestern Moffat Counties (BLM 2007b, p. 3:100), whereas the
previous 20 years resulted in 594 drilled wells (BLM 2007b, p. 3:99).
Similarly, the BLM anticipates between 17,800 and 21,200 new wells will
be drilled over the next 20 years in Rio Blanco and central and
northern Moffat Counties, whereas there were 5,800 wells drilled
previously (Seglund and Schnurr 2009, p. 129). However, the majority of
these wells will occur outside of the white-tailed prairie dog's
predicted range (Seglund and Schnurr 2009, p. 129). Approximately 96
percent of new wells will be drilled in areas with high oil and gas
potential as defined by the BLM (2007b, p. 3:100); we believe this
localizes the development to some extent and thus limits the amount of
prairie dog habitat impacted.
Three potential coal bed methane areas partially overlap white-
tailed prairie dog habitat in the Northwest IPA: eastern Sand Wash
Basin, Lower White River, and Danforth Hill (BLM 2007b, p. 3:102).
However, the majority of the coal bed methane areas occur outside the
predicted range for the species within Colorado (BLM 2007b, Figure 3-
16; Seglund and Schnurr 2009, p. 119).
Grand Valley-Uncompahgre IPA
There is potential for energy development to occur in a corridor of
the Grand Valley-Uncompahgre IPA in Mesa, Montrose, and Ouray Counties
(Seglund and Schnurr 2009, p. 54). Approximately 14 percent of the
white-tailed prairie dog's predicted range in this IPA is authorized
for lease or contains pending leases from the BLM (Seglund and Schnurr
2009, p. 131; Hotze 2010, p. 20). The BLM estimates authorizing 3,600
wells on 1,519 pads over the next 20 years in this IPA (Ewing 2009,
pers. comm.). The total area disturbed is estimated at 13,200 ac (5,342
ha) of short-term disturbance and 4,100 ac (1,659 ha) of long-term
disturbance (Ewing 2009, pers. comm.). We do not know where this
development will occur with respect to known prairie dog colonies.
However, 85 percent of this IPA remains unleased, and future wells
represent a relatively small (less than 2 percent of this IPA) amount
of additional disturbance.
North IPA
Crude oil was historically produced in the North IPA to a limited
degree. However, EOG Resources discovered a large reservoir of crude
oil in this area in 2008, and subsequently acquired a lease for 100,000
ac (40,469 ha) of land in the area (Seglund and Schnurr 2009, p. 129).
Approximately 25 percent of the white-tailed prairie dog's predicted
range in the North IPA has authorized or pending leases (Seglund and
Schnurr 2009, p. 131; Hotze 2010, p. 20).
In summary, BLM has authorized and has pending leases on
approximately 30 percent of the predicted range of the species within
Colorado for oil and gas development (Seglund and Schnurr 2009, p. 131;
Hotze 2010, p. 20). The largest potential for overlap and impacts to
white-tailed prairie dogs occurs in the Northwest IPA; oil and gas
development is projected to increase substantially in this IPA over the
next 20 years (Seglund and Schnurr 2009, p. 129). We expect the
majority of future oil and gas development to occur in this IPA. We do
not know the exact locations of energy development facilities with
respect to locations of white-tailed prairie dog colonies. Oil and gas
development will likely impact white-tailed prairie dogs, causing
individual mortalities and habitat loss and fragmentation. However, the
majority of oil and gas development will occur in
[[Page 30346]]
areas of high potential energy reserves, and particularly in the
Northwest IPA, so impacts to the species are likely to be more
localized, and are not expected to occur at high levels across the
species' predicted range in Colorado. Based on the available
information, we do not believe oil and gas development in Colorado is a
threat to the species now or in the foreseeable future.
Montana
White-tailed prairie dog habitat in Montana represents less than 1
percent of the gross range of the species (Seglund et al. 2006, p. 91),
and is contained entirely within Carbon County. Therefore we did not
calculate the area impacted by oil and gas leasing. The area containing
the South Sage Creek white-tailed prairie dog colony was leased in
January 2002, but is not yet developed (Begley 2010a, pers. comm.). The
South Sage Creek colony occupies less than 6 ha (15 ac), or 5 percent
of the occupied habitat in Montana (MFWP 2009b, p. 3). The area
containing the Robertson Draw colony is available for leasing but has
not yet been leased (Begley 2010a, pers. comm.). Oil and gas
development is not impacting the remaining six colonies in Montana
(Seglund et al. 2006, p. 26). Because of the small amount of habitat
impacted, oil and gas development is not a significant threat in this
State, now or in the foreseeable future.
Utah
The BLM has authorized oil and gas leases on 31 percent of the
white-tailed prairie dog's gross range in Utah (Hotze 2010, p. 18). The
highest overlap between the gross range of the white-tailed prairie dog
and oil and gas development potential occurs in Uintah, Duchesne,
Grand, and Carbon Counties (Hotze 2010, pp. 21-22; Utah Department of
Natural Resources 2004 in Seglund et al. 2006, p. 33).
The Uinta and Piceance Basin areas of Utah have significant oil and
gas resources (BLM 2008a, p. 3:38). Approximately 82 percent of 18,982
existing well locations in Utah occur in the Uinta Basin in Duchesne
and Uintah Counties (Hotze 2010, pp. 15-16). There are 97,266 ha
(240,350 ac) of mapped occupied white-tailed prairie dog habitat in
Uinta and Duchesne Counties (Hotze 2010, pp. 7-8). The BLM has
authorized oil and gas leasing on approximately 51 percent of this
mapped occupied habitat (Hotze 2010, p. 22). The BLM estimates that
approximately 2,055 new oil wells, 4,345 new gas wells, and 130 new
coal bed methane wells will be drilled within the Uinta Basin during
the 15- to 20-year planning period (BLM 2008a, p. 3:36). Approximately
73 percent of the Federal mineral rights open to leasing in the Uinta
Basin area have already been authorized (Hotze 2010, p. 24). Therefore,
the authorized leases represent a fair assessment of the potential
impact to white-tailed prairie dogs. These leases have a 201-meter
(660-ft) no surface occupancy stipulation adjacent to occupied prairie
dog colonies, which will minimize direct mortality of prairie dogs and
the loss of habitat from future development (see Factor D. Inadequacy
of Regulatory Mechanisms, below, for a discussion of these
stipulations).
There are 14627 ha (36,144 ac) of mapped white-tailed prairie dog
habitat in Carbon and Emery Counties (Hotze 2010, p. 8). The BLM has
authorized oil and gas leasing on approximately 52 percent of this
occupied mapped habitat (Hotze 2010, p. 22). About 2300 ha (5,600 ac)
(15 percent) of this habitat is located within areas considered to have
high potential for oil and gas resources (BLM 2004, p. 4:119). These
leases also have a no surface occupancy stipulation for prairie dog
colonies (see Factor D).
In summary, oil and gas leasing and development is authorized by
BLM across 31 percent of the species' gross range in Utah. The majority
of current and future project development occurs in the Uinta Basin in
northeastern Utah, and thus potential impacts to the species could be
greatest in this area, particularly because 52 percent of the species'
mapped occupied habitat is leased. We consider the Uinta Basin to be
the highest potential development area in Utah. Exploration and
drilling, as previously discussed, can result in mortality of
individual prairie dogs and the loss and fragmentation of habitats.
However, robust white-tailed prairie dog colonies continue to persist
in the Uinta Basin, in areas associated with existing oil and gas
development. The BLM imposes a no surface occupancy stipulation that
prohibits activity within 201 meters (660 ft) of white-tailed prairie
dog colonies in the Uinta Basin (see Factor D), which will minimize
direct mortality of prairie dogs and the loss of habitat from future
development. The likely concentration of oil and gas development in
high potential resource areas should also minimize the amount of white-
tailed prairie dog habitat directly lost to development. Due to these
factors, we do not believe oil and gas development in Utah is a threat
to the species now or in the foreseeable future.
Wyoming
Seventy-seven percent of the species' gross range in Wyoming
overlaps potential energy resources in Wyoming (Seglund et al. 2006, p.
39). However, not all potential energy resources will be developed.
Therefore, we further reviewed leases and potential energy resources to
determine the extent of development in the foreseeable future (the next
20 years).
Approximately 3,443,269 ha (88,508,503 ac) of land, or 27 percent
of the species' gross range in Wyoming, is authorized for leasing by
BLM (Hotze 2010, p. 18). These leases are either producing or are non-
producing. However, we expect the majority of new wells will be drilled
in areas with high oil and gas potential. In high and moderate
potential areas in Wyoming, a single well can produce 4 to 30 times as
much as a well in low potential areas (BLM 2008b, p. A20:6). Most wells
will be drilled in areas of high potential oil and gas resources
(Copeland et al. 2009). Only 415,649 ha (1,027,057 ac), or 4.2 percent
of the species' predicted range in Wyoming, occurs in high potential
oil and gas resource in areas as defined by Seglund et al. (2006, p.
39). Low and medium potential oil and gas resources overlap 73 percent
of the gross range of white-tailed prairie dog (Seglund et al. 2006, p.
39). Twenty-three percent of the gross range has no oil or gas
resources. Given the existing development, we consider the area in
southern Wyoming between Rawlins and Rock Springs to be a high
potential area (Hotze 2010, p. 11).
Oil and gas development and reserves occur throughout the gross
range in Wyoming. We do not know the exact locations of future energy
development facilities with respect to locations of white-tailed
prairie dog colonies. Oil and gas development will likely impact white-
tailed prairie dogs, causing individual mortalities and habitat loss
and fragmentation. However, as previously discussed, only a small
portion (4.2 percent) of the species' gross range overlaps areas of
high potential energy reserves. Energy development is most likely to be
concentrated in areas of high potential reserves, so impacts to the
white-tailed prairie dog will not occur at high levels across the
species' entire gross range in Wyoming. Based on the available
information, we do not believe oil and gas development in Wyoming is a
threat to the species now or in the foreseeable future.
[[Page 30347]]
Summary of Oil and Gas Development
Table 2 (below) gives a summary of the percentage of BLM-leased
area for oil and gas in gross, predicted, and mapped occupied range, by
State. Generally, the area attributed to producing leases makes up a
small portion of the species' range, although up to 28 percent of the
species' gross range has been leased for potential development.
TABLE 2. Percentage of leased area for oil and gas in gross, predicted,
and mapped occupied range of the white-tailed prairie dog.
(Totals include a small amount of land authorized for leasing but not
yet leased; and therefore not included in the other two categories.)
------------------------------------------------------------------------
Percent Percent Non- Total
State Producing Producing Percent
Leases Leases Leased*
------------------------------------------------------------------------
Colorado (Gross) 9 20 30
------------------------------------------------------------------------
Northwest IPA 7 34 41
(Predicted)
------------------------------------------------------------------------
North IPA (Predicted) 2 22 25
------------------------------------------------------------------------
Grand Valley/ 3 11 14
Uncompahgre IPA
(Predicted)
------------------------------------------------------------------------
Total, Predicted range 5 25 30
------------------------------------------------------------------------
Utah (Gross) 10 19 31
------------------------------------------------------------------------
Uintah Basin (mapped 17 32 51
occupied)
------------------------------------------------------------------------
Carbon and Emery 4 48 52
Counties (mapped
occupied)
------------------------------------------------------------------------
Wyoming (Gross) 6 21 27
------------------------------------------------------------------------
Total (Gross) 7 20 28
------------------------------------------------------------------------
Oil and gas development is a major cause of development in the
gross range of the species and is likely to continue into the
foreseeable future at similar rates of development. Twenty-eight
percent of the species' gross range is authorized for leasing. Leasing
does not guarantee development, and therefore we consider the area
leased Federally to be an estimate of the rangewide development,
including non-Federal estate. A minimum of 13,000 additional wells will
be authorized in the foreseeable future. However, energy development
will not occur uniformly across the landscape. Most development will
occur in areas of high resource potential. Development is also mediated
by variations in well density and spacing. There are localized regions
across the white-tailed prairie dog's gross range where development is
most prevalent, including the Uinta Basin in Utah, the Northwest IPA in
northwestern Colorado, and the southwestern region of Wyoming. The
impacts to white-tailed prairie dogs would thus be greater in these
locations than in other parts of the species' gross range.
In areas where energy development overlaps occupied white-tailed
prairie dog habitats, the resulting habitat loss and fragmentation
likely has negative effects on individuals and populations, including
mortality, noise disturbance, and habitat loss and fragmentation.
Presumably, there is a threshold level wherein habitat loss and
fragmentation may threaten the white-tailed prairie dog, at least in
localized regions. However, our available information indicates energy
development does not currently significantly threaten the species; for
example, large prairie dog complexes continue to persist in areas of
high energy development (see Colorado and Utah, above). Based on the
information available to us, we have determined that oil and gas
development does not significantly threaten the white-tailed prairie
dog now or in the foreseeable future.
Development of Oil Shale, Tar Sands, and Other Minerals
Extraction of oil shale and tar sands results in the removal of
wide swaths of habitat. Oil shale and tar sands development results in
a loss of habitat of the entire lease, although only portions of the
lease would be impacted at a given time. Impact footprints for oil
shale leases for strip mines are approximately 2,331 ha (5,760 ac) in
size (BLM 2008c, p. 4:4), and each surface retort mine (an underground
mine with processing of the material above ground) is approximately 668
ha (1,650 ac) (BLM 2008c, p. 4:8). When an area is processed, the
impact footprint shifts to another portion of the lease, and mined
areas are reclaimed. The success of reclamation varies dependent on
site conditions (BLM 2008c, p. 4:71). Oil shale and tar sand
development activities can result in long- term or permanent habitat
loss and fragmentation of white-tailed prairie dog habitats (BLM 2008c,
p. 4:109) depending on the quality and success of habitat reclamation.
Oil shale and tar sands resources occur across 8 percent of the
gross range of the species (Hotze, 2010, p. 34). Approximately
1,228,100 ha (3,034,696 ac) of potentially productive land for oil
shale and tar sands occurs in Wyoming and Utah (BLM 2008c, p. 2:113),
and the BLM made available 660,215 ha (1,631,424 ac) of Federal land
for leasing in this area (BLM 2008c, p. ES:7). A very small portion of
the white-tailed prairie dog's gross range is identified for leasing in
Colorado (Seglund and Schnurr 2009, p. 121).
Oil shale and tar sands development has failed to materialize due
largely to technological problems and unfavorable economics.
Significant economic questions remain regarding the development of the
Green River formation oil shale and tar sands resources (Bartis et al.
2005, pp. 15, 53; BLM 2006, pp. 7, 15-19, 31, 34-36). The cost
associated with an essentially new industry using new and innovative
technologies is likely to be great.
[[Page 30348]]
Economic success of oil shale- and tar sands-derived petroleum will
depend on continuing high and stable petroleum prices. Due to past
fluctuation of petroleum prices, private industry has exhibited a
reluctance to proceed with research, development, and subsequent
commercial production of oil shale. This situation will likely continue
unless the petroleum industry is convinced that petroleum prices will
remain high well into the future (Bartis et al. 2005, pp. 59-61; Bunger
et al. 2004, pp. 7-9).
Oil shale and tar sands extraction and development remains a
speculative industry. At this time, we believe it is unlikely that the
BLM will begin leasing the identified properties for development within
the foreseeable future, which we define as approximately 10-15 years.
In addition, while oil shale and tar sands resources overlap 8 percent
of the species' gross range, actual oil shale and tar sands development
facilities overlap with only a small portion (less than 0.1 percent) of
the species' gross range. We do not believe development of oil shale
and tar sands is a significant threat to the species now or in the
foreseeable future.
Mineral Development
Coal, uranium, sand, and gravel mining can result in the removal of
habitat (BLM 2004, p. 4:12). These activities have the potential to
result in long-term or permanent habitat loss and fragmentation,
depending on the quality and success of habitat reclamation. These
activities are not common land uses on BLM holdings in the gross range
of the species. The BLM solid mineral leases total 108,170 ha (445,209
ac), less than 1 percent of the species' gross range (Hotze 2010, p.
30). The BLM coal leases total 88,167 ha (217,866 ac), also less than 1
percent of the species' gross range (Hotze 2010, p. 32). Available
evidence does not suggest solid mineral leases are more common on
private lands. Available information does not suggest they will become
more widespread within the species' gross range in the future. Given
the small percentage of the gross range impacted by these activities,
we do not believe mineral development is a significant threat to the
species now or in the foreseeable future.
Renewable Energy Development--Wind and Solar
The BLM has accessed areas of renewable resource potential with the
objective of allowing the industries to focus development in the areas
of highest potential (BLM and DOE 2003, p. 2). The majority of the
species' gross range (Federal and non-Federal lands) has a low (~ 5kWh/
m2/day) amount of direct solar resources (BLM and DOE 2003, p. A2).
Currently, less than 1 percent of the species' range has been leased by
BLM for development of solar resources (BLM 2009, unpublished data). We
are unaware of solar developments on private land within the gross
range of the species. The majority of the land containing the species'
range is federally owned, and therefore we consider potential solar
developments on non-Federal land to be insufficient to threaten the
species. Given the limited solar resources and lack of development to
date in the species' range, we do not consider solar energy to be a
significant threat to the species now or in the foreseeable future.
Wind energy could impact the species by creating habitat loss,
disturbance, or fragmentation; increasing the amount of invasive
vegetation; increasing direct mortality; and increasing disturbance
from noise and human presence (BLM 2005b, p. 5:42). Wind power has
experienced a rate of expansion greater than any other renewable energy
resource, and continued increases are predicted through 2030 (EIA 2009,
pp. 47, 74). Depending on costs, wind power production could increase
nationwide by as much as 38 percent by 2030 (EIA 2009, p. 74).
The BLM manages more land areas of high wind resource potential
than any other land management agency. In 2005, the BLM completed the
Wind Energy Final Programmatic Environmental Impact Statement (EIS)
that provides an overarching guidance for wind project development on
BLM-administered lands (BLM 2005b, entire). Best management practices
are prescribed to minimize impacts of all phases of construction and
operation of a wind production facility. We do not have information on
how or where the EIS guidance was applied since 2005 and, therefore,
cannot evaluate its effectiveness.
Wind energy developments leased by the BLM total 823,358 ha
(2,034,562 ac), or approximately 4 percent of the species' gross range
(Hotze 2010, p. 28). Only 5 to 10 percent of a development will have
long-term surface disturbances (i.e., roads, foundations, substation,
fencing) (BLM 2005b, p. 5:2).
To evaluate the potential of future wind energy developments to
impact the species, we examined the potential locations for
development. Within the species' gross range in Colorado and Utah, only
poor and marginal wind power resources exist (NREL 2003, entire; NREL
2004, entire). In Wyoming, there are pockets of good, excellent, and
outstanding wind power within the species' gross range in Fremont,
Natrona, and Carbon Counties (NREL 2002, entire). The majority (more
than 75 percent) of these counties are federally owned land. However,
better wind power resources (rated as outstanding and superb, based on
wind speeds) are available east of the species' gross range (NRE