Endangered and Threatened Wildlife and Plants; Withdrawal of the Proposed Rule To List the Mountain Plover as Threatened, 27756-27799 [2011-11056]
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ADDRESSES).
If you use a
telecommunications device for the deaf
(TDD), call the Federal Information
Relay Service (FIRS) at 800–877–8339.
SUPPLEMENTARY INFORMATION:
DEPARTMENT OF THE INTERIOR
Fish and Wildlife Service
50 CFR Part 17
[Docket No. FWS–R6–ES–2010–0038; MO
92210–0–0008–B2]
Background
RIN 1018–AX26
Endangered and Threatened Wildlife
and Plants; Withdrawal of the
Proposed Rule To List the Mountain
Plover as Threatened
Fish and Wildlife Service,
Interior.
ACTION: Proposed rule; withdrawal.
AGENCY:
We, the U.S. Fish and
Wildlife Service (Service), announce our
decision to withdraw the proposed
listing of the mountain plover
(Charadrius montanus) as a threatened
species under the authority of the
Endangered Species Act of 1973, as
amended (Act). After a thorough review
of all available scientific and
commercial information, we have
determined that the species is not
endangered or threatened throughout all
or a significant portion of its range. We
make this determination because threats
to the species as identified in the
proposed rule are not as significant as
earlier believed and currently available
data do not indicate that the threats to
the species and its habitat, as analyzed
under the five listing factors described
in section 4(a)(1) of the Act, are likely
to endanger the species in the
foreseeable future throughout all or a
significant portion of its range.
DATES: The December 5, 2002 (67 FR
72396), proposal to list the mountain
plover as a threatened species is
withdrawn as of May 12, 2011.
ADDRESSES: This finding is available for
viewing on the Internet at https://
www.regulations.gov (see Docket No.
FWS–R6–ES–2010–0038) and https://
www.fws.gov/mountain-prairie/species/
birds/mountainplover and also by
appointment, during normal business
hours, at the U.S. Fish and Wildlife
Service, Colorado Ecological Services
Office, 134 Union Boulevard, Suite 670,
Lakewood, CO 80225; telephone 303–
236–4773; facsimile 303–236–4005.
Please submit any new information,
materials, comments or questions
concerning this finding to the Colorado
Ecological Services Field Office at P.O.
Box 25486, DFC (MS 65412), Denver,
Colorado 80225.
FOR FURTHER INFORMATION CONTACT:
Susan Linner, Field Supervisor, U.S.
Fish and Wildlife Service, Colorado
Ecological Services Field Office (see
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SUMMARY:
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Previous Federal Actions
For a detailed description of Federal
actions concerning the mountain plover,
please refer to the February 16, 1999,
proposed rule to list the species (64 FR
7587); the December 5, 2002, proposed
rule to list the species with a special
rule under section 4(d) of the Act (16
U.S.C. 1531 et seq.) (67 FR 72396); and
the September 9, 2003, withdrawal of
the proposed rule to list the species (68
FR 53083).
The document we published on
September 9, 2003 (68 FR 53083),
withdrew the entire proposed rule we
published on December 5, 2002 (67 FR
72396), including our proposal to list
the mountain plover as a threatened
species and our proposed special 4(d)
rule. The September 9, 2003, document
also addressed comments we received
on both the 1999 and 2002 proposals to
list the mountain plover and
summarized threat factors affecting the
species. The withdrawal of the proposed
rule was based on our conclusion that
the threats to the mountain plover
identified in the proposed rule were not
as significant as previously believed and
that currently available data did not
indicate that threats to the species and
its habitat, as analyzed under the five
listing factors described in section
4(a)(1) of the Act, were likely to
endanger the species in the foreseeable
future throughout all or a significant
portion of its range.
On November 16, 2006, Forest
Guardians (now WildEarth Guardians)
and the Biological Conservation
Alliance filed a complaint in the District
Court for the Southern District of
California challenging the September 9,
2003, withdrawal of the proposal to list
the mountain plover (68 FR 53083). We
entered into a settlement agreement
with the plaintiffs, which was filed by
the court on August 28, 2009. As part
of the settlement agreement, we agreed
to reconsider our decision to withdraw
the proposed listing of the mountain
plover and to submit to the Federal
Register by July 31, 2010, a document
reopening the December 5, 2002,
proposal to list the mountain plover (67
FR 72396) that would also request
public comments. We agreed to vacate
our 2003 withdrawal of the proposed
rule upon publication of the Federal
Register notice reopening public
comment on the December 5, 2002,
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proposal to list the mountain plover (67
FR 72396). We further agreed to submit
a final listing determination for the
mountain plover to the Federal Register
no later than May 1, 2011.
On June 29, 2010, we published a
document in the Federal Register
notifying the public that we were
reinstating that portion of our December
5, 2002, proposed rule to list the
mountain plover as threatened under
the Act (75 FR 37353). We did not
reinstate that portion of the December 5,
2002, proposed rule regarding a
proposed special rule under section 4(d)
of the Act. The proposed special rule
was designed to allow researchers to
complete field research and analyze
data for an ongoing study, and
addressed agricultural activities only
through December 31, 2004. To ensure
that our review of the species’ status
was complete and based on the best
available scientific and commercial
information, we requested comments on
the proposal to list the mountain plover
as a threatened species, including all
information related to the species’ status
and the proposed listing. We invited
public comments on the proposed
listing, new information relevant to our
consideration of the status of the
mountain plover, and comments and
information regarding threats to the
species and its habitat.
Species Information
Our February 16, 1999, and December
5, 2002, proposed rules (64 FR 7587 and
67 FR 72396, respectively), and our
September 9, 2003, withdrawal of our
2002 proposal to list the mountain
plover (68 FR 53083) described the
species’ life history, ecology, and habitat
use. For additional background on the
natural history of the mountain plover,
see the account of the species in The
Birds of North America (Knopf and
Wunder 2006).
While the majority of relevant
information directly pertaining to the
mountain plover that has become
available since our December 5, 2002,
proposal to list (67 FR 72396) and
September 9, 2003, withdrawal of that
proposal (68 FR 53083) has resulted
from local or Statewide studies on the
mountain plover’s breeding range; two
recent documents provide extensive
review of current knowledge regarding
the mountain plover:
(1) Mountain Plover (Charadrius
montanus) in Birds of North America
(Knopf and Wunder 2006); and
(2) Conservation Plan for the
Mountain Plover (Charadrius
montanus), Version 1.0 (Andres and
Stone 2009).
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Numerous other recent documents are
summarized in our June 29, 2010,
notification reinstating our December 5,
2002, proposed rule to list the mountain
plover as threatened under the Act (75
FR 37353). These include over twenty
peer-reviewed journal articles, and
many other reports and summaries
relevant to the status of the mountain
plover that have become available since
2002.
The following sections highlight and
update information on the mountain
plover with emphasis on information
developed since 2002.
Taxonomy and Species Description
The mountain plover (Charadius
montanus) is a small bird in the order
Charadriiformes, family Charadriidae.
No subspecies are recognized. It is a
migratory, terrestrial shorebird
averaging 8 inches (21 centimeters) in
body length. Mountain plover are light
brown above and white below, but lack
the contrasting dark breast band
characteristic of several other plovers
such as the more common killdeer (C.
vociferus). Sexes are similar in
appearance.
Feeding Habits
Mountain plover feed on grounddwelling invertebrates and flying
invertebrates found on the ground,
primarily beetles, crickets, and ants.
They forage with a series of short runs
and stops, feeding opportunistically as
they encounter prey (Knopf and Wunder
2006, unpaginated).
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Breeding
Mountain plover return north to their
breeding sites in the western Great
Plains and Rocky Mountain States in
spring. They arrive at their breeding
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grounds in northeastern Colorado in late
March (Graul 1975, p. 6). Arrival is
earlier farther south and later in
Montana and at higher elevations in
South Park, Colorado (Knopf and
Wunder 2006). Mountain plover are
territorial during the breeding season,
with males defending territories shortly
after arrival (Knopf and Wunder 2006).
Mountain plover are generally
monogamous; they form pairs and begin
courtship on arrival at their breeding
grounds. Nests consist of a simple
ground scrape. Egg laying in
northeastern Colorado begins in late
April and extends through mid-June
(Graul 1975, p. 7). Graul (1973, p. 84)
described mountain plover nesting as a
‘‘rapid multi-clutch system.’’ The female
normally produces two clutches,
typically three eggs each, at different
nest sites; the male incubates the first
nest site while the female incubates the
second. If the first nest or brood is lost
early in the breeding season, the adult
may renest, so each pair can potentially
make four attempts per year to raise a
brood. This breeding system may
increase breeding success given
predation that occurs on mountain
plover nests or broods. This breeding
system, rare among bird species, may
result in greater reproductive potential
than in other shorebirds (Knopf and
Wunder 2006). It may have developed
in response to food fluctuations that
typically occur in the shortgrass prairie,
where insect populations likely
fluctuate in response to annual,
seasonal, and local fluctuations in
precipitation (Graul 1973, p. 85).
Average incubation period is 29 days
(Graul 1975, p. 19). Chicks leave the
nest within hours of hatching and
obtain their own food. Only one adult
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normally tends each nest and brood.
The minimum habitat requirement for
mountain plover broods in Montana was
70 acres (ac) (28 hectares (ha)) (Knopf
and Rupert 1996, p. 33), and brood
home ranges averaged 143 ac (57 ha) on
rangeland in Colorado (Knopf and
Rupert 1996, p. 31). Brood home ranges
appeared similar for three Colorado
landscapes (Dreitz and Knopf 2007, p.
129). Parents stay with chicks until they
fledge, which occurs at about 33 to 34
days (Graul 1975, p. 25). Mountain
plover breed their first spring and every
year thereafter (Knopf and Wunder
2006).
Habitat and Range
Although often thought of as a
grassland species, the mountain plover
may best be described as a species of
disturbed prairie or semi-desert habitat
(Knopf and Miller 1994, p. 505). They
are found on open, flat lands including
xeric (extremely dry) shrublands,
shortgrass prairie, barren agricultural
fields, and other sparsely vegetated
areas. On grasslands, they often inhabit
areas with a history of disturbance by
burrowing rodents such as prairie dogs
(Cynomys spp.), native herbivores, or
domestic livestock.
Mountain plover breed from Canada
(extreme southern Alberta and
Saskatchewan) to northern Mexico
(Figure 1) with greatest apparent
numbers in Colorado and Wyoming, and
substantial numbers in Montana, New
Mexico, and Nebraska. In Mexico,
breeding populations are suspected in
the States of Chihuahua, Cohuila, and
Nuevo Leon (Andres and Stone 2009,
p. 9).
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Breeding Habitat
Mountain plover winter in similar
habitat, many in California, but also in
southern portions of Arizona, Nevada,
New Mexico, Texas, and in northern
Mexico. While California’s Sacramento,
San Joaquin, and Imperial Valleys
support the greatest documented
concentrations of wintering mountain
plover, relatively little is known about
wintering numbers or distribution in
other areas.
Common elements of mountain plover
breeding habitat include short
vegetation, bare ground, and flat
topography. The mountain plover
historically nested in a region impacted
by a variety of herbivores, including
prairie dogs, bison (Bison bison), and
pronghorn antelope (Antilocapra
americana), because these heavily
grazed or similarly disturbed landscapes
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support reduced height and density of
vegetation, creating favorable breeding
habitat for mountain plover. While the
mountain plover is categorized as a
shorebird, it is seldom found near
margins of freshwater or marine
estuaries. Dinsmore (2003, pp. 14–17)
described four types of breeding habitat:
Short- and mixed-grass prairie, prairie
dog colonies, agricultural lands, and
semi-desert.
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On the plains, the mountain plover is
generally considered an associate of the
shortgrass prairie, dominated by blue
grama (Bouteloua gracilis) and buffalo
grass (Buchloe dactyloides) (Knopf and
Miller 1994, p. 504). In the Pawnee
National Grasslands (PNG) in northern
Weld County, Colorado, an area that
formerly supported the greatest known
concentration of breeding mountain
plover, breeding habitat was described
as restricted to flat, heavily grazed areas
(Graul 1973, p. 69). Native prairie
grasslands formerly presented a diverse
ecosystem, shaped by low precipitation,
grazing, and fire. Today, prairie
landscapes often consist of grassland
fragments where current cattle grazing
practices tend to create relatively
uniform grass coverage and height,
which is not beneficial to mountain
plover (Knopf 2008, pp. 55–57). Typical
range management practices such as
rotational grazing, limited grazing, and
improving soil moisture are designed to
promote taller grasses that limit
mountain plover use. Within these
landscapes, areas of cattle concentration
(loafing areas and near water),
disturbance caused by prairie dogs, and
plowed or fallow (unseeded for one or
more seasons) agricultural fields create
conditions favorable for mountain
plover nesting (Knopf and Wunder
2006). Mountain plover are also
attracted to burned areas in their
breeding grounds, and burning may be
valuable as a habitat management tool
(Knopf 2008, pp. 25–26, 57–58, 61;
Andres and Stone 2009, p. 34).
Prairie dog colonies create important
habitat for mountain plover, and are
especially important to maintaining
mountain plover populations in the
northern portions of their range
(Dinsmore et al. 2003, pp. 1024–1025;
Dinsmore et al. 2005, p. 1552;
Augustine et al. 2008, unpaginated;
Childers and Dinsmore 2008, p. 705;
Tipton et al. 2009, pp. 496–497; Dreitz
2009, pp. 875–877). Active prairie dog
colonies provide exposed soils around
burrows and, because prairie dogs keep
surrounding vegetation clipped, an area
of low-growing, perennial vegetation
that is suitable as mountain plover
breeding and brood-rearing habitat. In
addition, prairie dogs give alarm calls in
response to the approach of predators
and may alert mountain plover to
predator presence. The density of
mountain plover was found to be much
greater on black-tailed prairie dog (C.
ludovicianus) colonies than on other
habitats in Montana (Childers and
Dinsmore 2008, pp. 705–706). In northcentral Montana, the size of the adult
mountain plover population closely
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tracked annual changes in the area
occupied by black-tailed prairie dogs
(Dinsmore et al. 2003, p. 1024). Both
prairie dog and mountain plover
numbers declined sharply in the mid1990s in response to an outbreak of
sylvatic plague, which caused deaths of
prairie dogs and resultant loss of
favored mountain plover habitat.
Mountain plover later increased in
concert with subsequent increases in
prairie dogs (Dinsmore et al. 2005, pp.
1550–1552).
In the Colorado shortgrass prairie
ecosystem, mountain plover densities
observed on black-tailed prairie dog
colonies were higher than those on
dryland agriculture and much higher
than those on grasslands without prairie
dogs (Dreitz et al. 2006, p. 702; Tipton
et al. 2009, p. 496). Mountain plover
were significantly more abundant on
black-tailed prairie dog colonies than on
other rangeland within a bison pasture
in northeastern New Mexico (Groguen
2010, pers. comm.). Prairie dog colonies
occupied by mountain plover were, on
average, larger in size than colonies
with no mountain plover. In Utah,
mountain plover nested in proximity to
white-tailed prairie dog (C. leucurus)
colonies (Manning and White 2001, p.
226). In northeastern Mexico, breeding
mountain plover were associated with
Mexican prairie dog (C. mexicanus)
colonies (Gonzales-Rojas et al. 2006, p.
82).
Mountain plover have been found to
regularly use fallow or plowed
agricultural fields for nesting (Shackford
et al. 1999, entire; Dreitz and Knopf
2007, pp. 684–685; Bly et al. 2008, p.
127; McConnell et al. 2009, pp. 30–33).
Where mountain plover have an
opportunity to choose between
agriculture and prairie, they may use
both equally (Knopf and Rupert 1999, p.
84). Shackford et al. (1999, entire) found
mountain plover nesting on cultivated
fields in Colorado, Oklahoma, Kansas,
and Wyoming. Fifty percent of all nests
they encountered during their research
were on fallow or bare fields. While
many nests were destroyed by farm
machinery, they concluded that
mountain plover were using cultivated
fields successfully for nesting,
especially in southern portions of the
species’ range (Shackford et al. 1999, p.
117).
Recent studies addressed the
mountain plover’s nesting ecology, and
attempted to identify the extent of
breeding distribution and population
size in Nebraska (Bly et al. 2008). They
encountered 272 nests on agricultural
fields of cultivated wheat and millet
(Bly et al. 2008, p.123). Studies in
Oklahoma encountered mountain plover
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on bare agricultural fields (90 percent of
observations), with few (5 percent of
observations) associated with prairie
dog towns (McConnell et al. 2009, pp.
31–32).
It remains unknown whether Texas or
Mexico crop fields support mountain
plover breeding (Andres and Stone
2009, p. 24). Holliday (2010) reported
that breeding season sightings of
mountain plover from the Texas
Panhandle tended to be in cultivated
fields as in adjacent Oklahoma,
although previously reported nesting in
West Texas was in grazed, short-grass
habitat.
Knopf and Wunder (2006) described
mountain plover as breeding ‘‘more
predictably’’ at semi-desert locations
west of the shortgrass prairie in
Colorado, Wyoming, and Montana.
Beauvais and Smith (2003, entire)
developed a model of mountain plover
breeding habitat in shrub-steppe habitat
of western Wyoming. They related
favored patches of mountain plover
breeding habitat to poor soils, low
precipitation, and wind scour, features
they predicted would persist over time,
especially on public lands. In such
habitats, mountain plover are less
dependent on prairie dog colonies to
create breeding habitat. A Wyoming
study located 55 mountain plover nests
in grassland or desert scrub habitat in
six counties (Plumb et al. 2005a, p. 225).
All nest sites were grazed by ungulates
with prairie dogs present at only 36
percent of nest sites, mostly in grassland
(Plumb et al. 2005a, pp. 226–227). In
Montana, Childers and Dinsmore (2008,
p. 107) noted that sparsely vegetated,
hardpan clay flats provided nesting
habitat.
In summary, mountain plover require
short vegetation with some bare ground
on their breeding sites. In grasslands,
this usually requires disturbance, such
as that provided by prairie dogs, cattle
grazing, fire, or farming. In semi-desert
environments, breeding habitat may
persist without these forms of
disturbance.
Migration and Wintering Habitat
Southbound migration of mountain
plover is prolonged, with post-breeding
flocks numbering in the hundreds
forming in late June with some
remaining on breeding areas until
September or October (Bly et al. 2008,
p. 123; Andres and Stone 2009, p. 10).
Mountain plover migrate southward
across the southern Great Plains in late
summer and early fall to Texas, New
Mexico, and Mexico, with many then
traveling west to California (Knopf and
Wunder 2006). During spring migration,
mountain plover move from their
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wintering sites in early March and
proceed quickly to breeding sites in
eastern Colorado by mid-March and in
Montana by mid-April (Knopf and
Wunder 2006). Mountain plover are
generally thought to use habitats similar
to those on the breeding and wintering
grounds during migration. During
migration, they have also been reported
using alkaline or mud soils, and sod
farms (Knopf and Wunder 2006). Few
studies have been conducted on
stopover habitat, and little is known
about stopover ecology or food
resources exploited (Andres and Stone
2009, pp. 14, 21, 37).
In winter, mountain plover use
habitats similar to those on their
breeding grounds. Mountain plover are
found wintering in California mostly on
fallow and cultivated agricultural fields,
but also on grasslands and grazed
pastures (Hunting et al. 2001, p. 39;
Knopf and Wunder 2006).
Throughout the Central Valley of
California, the field types used by
mountain plover vary seasonally, from
uncultivated lands in October and
November, shifting toward cultivated
lands over the winter (Hunting and
Edson 2008, pp. 183–184). Mountain
plover wintering in the San Joaquin
Valley of California used tilled fields,
grazed pastures, alkali flats, and burned
fields, but they preferred native valley
sink scrub (low vegetation dominated by
alkali-tolerant shrubs) and nonnative
grazed or burned grasslands over any of
the more common cultivated land types
(Knopf and Rupert 1995, pp. 747–749).
Winter habitat availability in
California’s Carrizo Plain seems linked
to a combination of livestock grazing
and precipitation, with heavy grazing
and dry conditions creating conditions
most favorable to the mountain plover.
Giant kangaroo rat (Dipodomys ingens)
precincts (colonies) are also used,
especially when wet years produce tall
vegetation elsewhere (Sharum 2010,
pers. comm.).
Mountain plover exclusively used
cultivated sites in the Imperial Valley of
California (Wunder and Knopf 2003, pp.
74–75). While cultivated lands are
abundant throughout the Imperial
Valley, not all provide suitable feeding
habitat. Mountain plover were found to
favor irrigated farmland, including
burned bermudagrass (Cynodan
dactylon); harvested, grazed, or
sprouting alfalfa (Medicago spp.) fields;
and newly cultivated fields (Wunder
and Knopf 2003, pp. 75–76; AMEC
Earth and Environment 2003, p. 12).
Fallow fields were used mostly for
roosting, and melon and vegetable fields
were rarely or never used (Wunder and
Knopf 2003, pp. 75–76). Insect
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availability, furrow depth, size of dirt
clods, and the vegetation on contiguous
land parcels were all believed to
influence the suitability of agricultural
fields to mountain plover.
In California, annual climatic
variability, especially abundant rainfall,
influences field conditions and can
reduce mountain plover use of
traditionally occupied wintering sites.
For example, mountain plover became
virtually absent from cultivated fields in
the Imperial Valley during the rainy
winter of 2004–2005 (Knopf and
Wunder 2006). Movement patterns of
wintering mountain plover in California
are shown to be highly variable, with
birds on several occasions moving more
than 34 miles (mi) (55 kilometers (km))
in a week (Knopf and Wunder 2006).
In Arizona, mountain plover winter
on sod farms and grazed pastures, and
are observed using the same sites yearly.
Their use of farm fields and other
potential habitats is generally unknown,
and these areas are rarely surveyed
(Robertson 2010, p. 1). A few mountain
plover have wintered in recent years on
mowed grasses at Gila Bend Air Force
Auxiliary Field (Mendelsohn 2010).
In Texas, winter reports of mountain
plover were correlated with barren
fields and grazed pastures (Holliday
2010). In Williamson and Bell Counties,
Texas, mountain plover winter only on
large, flat, plowed fields, especially
those with some corn or sorghum
stubble (Fennel 2002, p. 29). In the
Texas coastal bend area (Nueces and
San Patricio Counties), wintering plover
are largely limited to plowed fields
rather than grasslands or fallow fields,
with mountain plover often following
tractors while feeding (Cobb 2009, pers.
comm.). Wintering mountain plover in
Texas have also been reported using
burned fields (Knopf and Wunder 2006),
sod farms (Cobb 2011, pers. comm.),
coastal prairies, and alkaline flats
(Andres and Stone 2009, p. 12).
In Mexico, mountain plover are found
wintering in grassland areas with high
densities of prairie dogs (both blacktailed and Mexican) and on heavily
grazed pastures (Andres and Stone
2009, p. 12; Macias-Duarte and Panjabi
2010, pp. 5, 7). Consistent with other
areas, open habitat with low grass cover
and sparse or no shrub cover are
elements common to areas used by
mountain plover in Mexico. However,
significant mountain plover use of crop
fields in Mexico has not been reported
(Macias-Duarte and Punjabi 2010, p. 7).
Wunder (2007) studied geographic
population structure in mountain plover
through color-banding and stable
isotope concentrations in feathers. He
concluded that there is widespread
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mixing of mountain plover populations
in winter and that birds may use
alternate wintering sites in different
years (Wunder 2007, p. 118). While
mountain plover appear annually at
some favored wintering sites, site
fidelity by individual birds appears low.
Mountain plover can move long
distances and use various sites even
within a given winter.
Survival, Lifespan, and Site Fidelity
A long-term study on mountain
plover breeding grounds in Phillips
County, Montana, provides much of
what is known regarding population
dynamics of the species. The annual
survival rate of adult mountain plover of
both sexes in Phillips County ranged
from 0.74 to 0.96 yearly (Dinsmore
2008, p. 50). The annual survival rate
for juvenile mountain plover (survival
to 1 year of age) was 0.06 at hatching,
but for those chicks that reached
fledging age was 0.62 (Dinsmore 2008,
p. 51). Survival estimates did not
account for permanent emigration (birds
surviving but returning in subsequent
years to sites outside of the study area),
so the actual annual survival may have
been higher.
Previous estimates of survival rates
and of estimated mean lifespan of 1.92
years (Dinsmore et al. 2003, pp. 1020–
1021) supported our December 5, 2002,
conclusion that the mountain plover
had a shorter lifespan than other plovers
(Charadriidae) (67 FR 72397) and that
this might impact its opportunity to
reproduce. These conclusions
underestimated adult mountain plover
survival. The longer study of the same
population over years with varying
weather and habitat conditions
modified the earlier conclusions
regarding the mountain plover’s
longevity. Mountain plover of 5 to 7
years of age were frequently
encountered, and a longevity record
over 10 years was established (Dinsmore
2008, p. 52). Based on this additional
research, survival rates for mountain
plover appear comparable to those
reported for other plovers, and the
mountain plover is now considered a
relatively long-lived species (Dinsmore
et al. 2010, unpaginated). We no longer
believe that the mountain plover’s
lifespan is a liability that could
contribute to the negative impact of
natural or manmade events affecting the
species.
Mountain plover have a high nest
survival rate compared to other groundnesting species (Dinsmore et al. 2010),
but nest success in mountain plover has
varied greatly from study to study.
Successful hatching (of at least one egg)
ranged from 26 percent (Knopf and
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Rupert 1996, pp. 29–30) to 65 percent
(Graul 1975, p. 18). Dinsmore et al.
(2002, pp. 3485–3486) found differences
in nest success between nests incubated
by males (49 percent) and females (33
percent). Dreitz and Knopf (2007, p.
684) found nest success of 37 percent
with no appreciable difference between
nests on agricultural fields and on
native rangeland.
There have been relatively few studies
of chick survival (hatching to fledging)
and results vary greatly. Dreitz (2009, p.
6) estimated that 30-day survival of
chicks of mountain plover from prairie
dog colony nesting habitat was 75
percent, and that 30-day survival on
other grasslands and on agricultural
fields was less than 25 percent.
Following similar methodology,
research on crop fields in Nebraska
found 95 percent survival of chicks
accompanying 31 adult mountain plover
that were radio-tracked for the 36 days
after eggs hatched (Blakesley and
Jorgensen 2010). Radio contact was lost
with other adults (due to birds leaving
the area or transmitter failure), but even
if assuming all chicks associated with
these adults perished, chick survival
was at least 58 percent (Blakesley and
Jorgensen 2010). Dreitz et al. (2010)
studied post-hatching chick survival
(hatching to fledging) via radio-tracking
in Colorado and Montana. The study
targeted factors affecting survival,
including landscape characteristics,
with an objective of informing
conservation and management efforts.
Field studies in 2010 were hampered by
unusually cold and wet weather. Of 93
chicks radio-tracked over three habitat
types in Colorado, only 9 were
confirmed to survive to 30 days (Dreitz
et al. 2010, p. 3). Thirty-eight confirmed
mortalities included 13 from avian
predators, 8 from mammalian predators,
and 17 from unknown predation,
weather, and undetermined factors.
Contact with other chicks was lost, and
their fates were unknown. Results did
not reflect higher chick survival on
prairie dog towns than on other
grasslands or agricultural fields. In
Montana, only 1 of 39 chicks monitored
on black-tailed prairie dog colonies was
confirmed to survive to 30 days.
Nineteen mortalities were documented,
with 13 from heavy rains (Dreitz et al.
2010, p. 4). Sources of mortality differed
among habitats in Colorado, with avian
predation higher at black-tailed prairie
dog towns (Dreitz et al. 2010, p. 6).
However, results of the study are
considered preliminary, and future
work is planned.
Few studies have estimated seasonal
adult survival rates. Dreitz (2010,
unpaginated) found 89 percent survival
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of adults with broods for the 30 days
after hatching. A study of overwintering
mountain plover in California showed
nearly 95 percent survival of wintering
birds from November 1 to March 15
(Knopf and Rupert 1995, p. 746). Since
survival of adults during stationary
periods is believed to be relatively high,
and there is no estimate for adult
survival during spring and fall
migration, there is potential that losses
of adults during migration may be
significant and efforts to increase adult
survival might be focused on migration
periods (Dinsmore et al. 2003, p. 1023;
Andres and Stone 2009, p. 1; Dinsmore
et al. 2010). However, there is no
scientific information available to
indicate that high mortality during
migration is occurring.
A life stage-specific model based on
data from three breeding areas, two in
Colorado and one in Montana, found
that mean adult survival was the
parameter that most influenced modeled
population growth (Dinsmore et al.
2010). The importance of adult survival
was characterized as typical of longlived bird species, for which repeated
reproductive attempts throughout life
are less important to population growth,
as evidenced by low chick survival,
than adult survival (Dinsmore et al.
2010). Nest survival was comparable to,
or higher than, other ground-nesting
shorebirds and was less important to
population growth than survival of
chicks, juveniles, and adults. Large
variation in estimates of chick survival
led to the conclusion that to improve
population viability on breeding areas,
management to increase chick survival
should be a priority. The authors
believed such management should be
emphasized over past efforts to decrease
nest losses and increase hatching
success (Dinsmore et al. 2010).
However, the authors conceded that
management to improve chick survival
is more difficult than improving
hatching success and might require
large-scale habitat improvement.
Mountain plover were thought to have
high site fidelity to nesting locations,
returning to same area where they
hatched each year (Graul 1973, p. 71).
Skrade and Dinsmore (2010, p. 672)
quantified mountain plover dispersal on
breeding sites in Montana and reported
juvenile (natal) dispersal (hatching year
to return at age 1) averaged 8.1 mi (13.0
km) for males and 6.3 mi (10.2 km) for
females. Only 4 of 38 banded chicks
returning as adults arrived back at the
same black-tailed prairie dog colony
where they were banded. Knopf and
Wunder (2006) noted a chick that had
dispersed over 30 mi (50 km) in
Colorado.
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The previous year’s nesting success
influences adult dispersal; unsuccessful
adults disperse farther than successfully
breeding adults (Skrade and Dinsmore
2010, p. 671). While adults rarely move
far from the area where they nested the
previous year, evidence of potential for
year-to-year dispersal in adults is
exemplified by an adult mountain
plover banded on a breeding area in
Colorado in 2009, that was found
nesting approximately 25 mi (40 km)
away in Nebraska in 2010 (Bly 2010b,
pers. comm.).
Results from genetic studies suggest
that gene flow among breeding areas is
sufficient to offset genetic effects of
small populations and reported adult
fidelity to breeding areas (OylerMcCance et al. 2008, pp. 496–497).
Population Size and Trends
Mountain plover are difficult to detect
because they are cryptically colored and
in general are widely distributed at low
densities (Knopf and Wunder 2006).
Based on historical observations of
mountain plover and extensive habitat
changes, there is general agreement that
the mountain plover is currently greatly
reduced in numbers and range
compared to their numbers and range
prior to European settlement (Graul and
Webster 1976, p. 265; Knopf and
Wunder 2006). The mountain plover’s
historical breeding range is believed to
have differed from that currently
occupied primarily in its eastern extent,
which may have encompassed the
western thirds of North Dakota, South
Dakota, and Nebraska, and more of
western Kansas and the Texas
Panhandle than is currently occupied
(Graul and Webster 1976, p. 265, Knopf
and Wunder 2008).
Population estimates for the species,
both historical and recent, appear
imprecise. Graul and Webster (1976, p.
266) estimated that mountain plover
populations in Montana, Wyoming,
eastern Colorado, and New Mexico then
totaled 214,200 to 319,220 birds, with
20,820 in the population stronghold of
Weld County, Colorado. However,
Knopf and Wunder (2008) cited Graul
(pers. comm.) as saying that the
estimates may have been off (i.e., high)
by an order of magnitude (a factor of
10).
Knopf (1996, p. 12) estimated the total
population of mountain plover to be
about 8,000 to 10,000, based on a 1994
wintering survey in California and on
assumptions regarding proportion of the
wintering population observed (i.e., that
only half of birds wintering in California
had been counted and that 1,000 to
3,000 birds wintered in Texas and other
areas). We cited this estimate in our
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December 5, 2002, proposed rule (67 FR
72396). In our September 9, 2003,
withdrawal of our proposed listing (68
FR 53083), we again cited the Knopf
estimate above and, using similar
assumptions and newer California
winter survey data (1998–2002),
provided a rangewide estimate of 5,000
to 11,000 mountain plover. More recent
studies, which estimated populations
present on specific portions of the
breeding range, have resulted in a
higher rangewide estimate of the
mountain plover breeding population.
After investigating Wyoming
populations, Plumb et al. (2005b, p. 15)
estimated a minimum of 3,393
mountain plover in Wyoming (up from
previous estimates of 500 to 1,500) and
estimated a rangewide total of 11,000 to
14,000 mountain plover. Based on
newer information, including an
upward revision of estimated mountain
plover numbers on the eastern Colorado
plains (a conservative estimate of 8,577
birds), Tipton et al. (2009, p. 497)
provided a rangewide estimate of 15,000
to 20,000 mountain plover. Andres and
Stone (2009, p. 8) reviewed available
data and provided a coarse, minimum
rangewide estimate of 18,000 breeding
mountain plover. Knopf and Dreitz (in
press) concluded that the continental
breeding population is ‘‘certainly larger’’
than the 17,500 birds estimated in
Montana, Wyoming, and Colorado,
citing small populations in contiguous
States, a potentially significant
population in New Mexico, and an
unknown population in Mexico. Based
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on our review of recent data, including
those from Nebraska (Van der Berg et al.
2010) and New Mexico (see Breeding
Range below), we estimate that the
current rangewide mountain plover
breeding population exceeds 20,000
birds. This was supported by Knopf
(2009, pers. comm.). We have no
information to indicate that this
estimate reflects an actual increase in
rangewide mountain plover numbers
over previous, lower estimates. Instead,
it likely reflects the limitations of those
earlier rangewide estimates (based on
mountain plover wintering in California
that largely discounted birds wintering
elsewhere) and more accurate recent
estimates of breeding populations.
Accurate trend information for
mountain plover numbers is generally
lacking. Interpreting trends from the two
long standing surveys, the Breeding Bird
Survey (BBS) and the National Audubon
Society’s Christmas Bird Count (CBC),
suffer from a variety of problems,
including the inherent difficulties
associated with using a survey of only
a small portion of a total population to
infer rangewide trends (Knopf and
Wunder 2004, p. 1).
The BBS is a large-scale survey of
North American birds that began in
1966, and is conducted during the
breeding season by observers driving
along roads over established routes.
Knopf (1996, p. 12) cited BBS data from
1966 through 1993 as indicative of a
steep decline in mountain plover
numbers across their breeding range (3.7
percent per year, a decline of
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approximately two-thirds over the
period). However, Knopf and Wunder
(2004, p. 1) suggested that the timing of
surveys (which occur mostly in June
when mountain plover are less
conspicuous) and the low densities at
which mountain plover occur prevent
reliable trend estimates.
Based on recent BBS data analysis
(Sauer 2010a), the mountain plover has
declined rangewide at an estimated rate
of 2.6 percent per year for the period
from 1966 to 2009 (95 percent
confidence interval (CI) ¥6.7 to +0.6).
However, for the period from 1999
through 2009, the estimated rate of
decline decreased to 1.1 percent per
year (95 percent CI ¥5.8, +9.6) (Figure
2). While neither estimate varies
statistically from a stable population (at
a 95 percent CI), the probability that the
estimated long-term trend (1966 through
2009) is less than or equal to zero is 95
percent. The probability that the
estimated short-term trend (1999
through 2009) is less than or equal to
zero is 68 percent. The estimated longterm decline is consistent with the
generally accepted conclusion that the
mountain plover’s rangewide
population is currently smaller than it
was in the 1960s. The more recent (1999
through 2009) estimated decline and
associated CI lead us to conclude that
most or all of the long-term decrease
took place before 1999, that any recent
declines are modest, and that the
mountain plover population may be
near stable.
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Sauer (2011, pers. comm.) concluded
that limited regional data from the BBS
(i.e., the low numbers of routes
reporting the species and low numbers
of mountain plover observed) resulted
in imprecise trend estimates within
individual States and for the time
periods of interest. He also concluded
that BBS data only provide an imprecise
summary of mountain plover
population dynamics, and the limited
sample size likely reflects the
limitations of the roadside sampling
frame in sampling mountain plover
breeding populations.
We conclude that, while the BBS is
the only long-term trend information
available for the mountain plover on its
breeding range, it is an imprecise
indicator of mountain plover population
trends. Given the wide confidence
interval and the conclusion by Sauer
(2011, pers. comm.) above, the data
provide limited support for any recent
(1999 through 2009) trend in mountain
plover numbers. Even so, we
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acknowledge that this is the best
available information on trends for this
species and BBS survey results suggest
a recent (1999 through 2009) moderated
rate of decline (Figure 2). We provide
long-term and recent BBS trend
estimates for three States where the
sample size allowed for analysis (see
Conservation Status and Local
Populations below), but with the same
reservations regarding precision.
The CBC is an annual count
performed around the end of December
in which volunteers observe birds in 15mi (24-km) radius count circles. While
CBCs can be used to infer species
population trends, spatial coverage is
limited (Knopf and Wunder 2004, p. 1)
and established count circles commonly
coincide with populated areas where
volunteers are available. The CBC data
estimated an annual decrease of 2.8
percent in mountain plover observed
from 1966 through 2007, but reliability
was described as low (Butcher and
Niven 2007, Appendix 1).
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The vast majority of mountain plover
reported in CBCs come from California
and, within California, from the South
Salton Sea count. Pandolfino (2009,
unpaginated) submitted his analysis of
CBC data for California and recognized
the data’s limitations, but concluded
that the data reflected long-term and
recent declines in mountain plover
numbers wintering in California. The
CBC data on mountain plover numbers
is highly variable from year to year. The
Salton Sea South CBC, the only CBC in
the Imperial Valley, is limited in scope
and does not include portions of the
valley where most mountain plover
have been seen (Wunder and Knopf
2003, p. 76). Inherent limitations in data
collection methods (volunteers
surveying small areas relative to total
winter range) and lack of sufficient
detections of mountain plover in
California count circles (Hunting et al.
2001, p. 40) render trend analysis
uncertain. CBC data from other States
and Mexico is even less representative
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of wintering populations and provides
no insight into possible trends for the
mountain plover.
We conclude, based on observations
across the mountain plover’s range and
BBS trend data, that a historical decline
of the mountain plover has occurred
since the 1960s. However, we agree with
the conclusion of Andres and Stone
(2009, p. 3) that precise and accurate
information on recent trends in
mountain plover numbers is lacking.
The recent (1999 through 2009) decline
estimate from BBS data is modest (1.1
percent per year) and any difference
from a stable population estimate (slope
of 0.0) is statistically insignificant.
However, we acknowledge that the BBS
data is the best available information on
trends for the mountain plover and that
BBS results suggest a recent (1999
through 2009) moderated rate of decline
(Figure 2). The CBC wintering data are
highly variable and come mostly from
California, but also suggest a long-term
decline. No comprehensive trend data
across the mountain plover’s wintering
range are available. The discussion
below provides information on
populations and trends within States,
Canada, and Mexico, where available.
Conservation Status and Local
Populations
The mountain plover is listed as
endangered in Canada, as a sensitive
species in Alberta, and as a threatened
species in Mexico (Andres and Stone
2009, p. 13; Gober 2010). The mountain
plover is identified by the Service as a
Bird of Conservation Concern (Service
2008), is considered ‘‘highly imperiled’’
in the U.S. Shorebird Conservation Plan
(2004, p. 2), a category assigned to
species listed as threatened or
endangered nationally, and all species
with significant population declines and
either low populations or some other
high risk factor. It is also identified as
‘‘G3-vulnerable’’ by NatureServe (2010).
The species is listed as a sensitive
species by the U.S. Forest Service
(USFS) (2010) and by the Bureau of
Land Management (BLM) (2000a, 2006,
2010a). It is identified as a species of
global conservation concern in the
American Bird Conservancy and
National Audubon Watchlist, and it is
listed as ‘‘near threatened’’ by the
International Union for the
Conservation of Nature (IUCN) (BirdLife
International 2010). The designations
discussed above may, in part, reflect
population estimates at the time those
designations were established. The
IUCN previously (from 2004 to 2007)
listed the species as ‘‘vulnerable,’’ a
higher level of concern than ‘‘near
threatened,’’ but changed its rating as
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higher rangewide population estimates
emerged. The U.S. Shorebird
Conservation Plan provided a rangewide
estimate of 9,000 mountain plover until
2006, when the estimate was revised
upward to 12,500 (Morrison et al. 2006,
p. 69).
All States within the range of the
mountain plover have included the
species in their Comprehensive Wildlife
Conservation Strategy or Wildlife
Action Plans or both (State Plans)
(Arizona Game and Fish Department
2006; University of California 2005;
Colorado Division of Wildlife 2006;
Wasson et al. 2005; Montana Fish,
Wildlife and Parks 2005; Schneider et
al. 2005; New Mexico Department of
Game and Fish 2006; Oklahoma
Department of Wildlife Conservation
2005; Texas Parks and Wildlife 2005;
Wyoming Game and Fish Department
2005) as either ‘‘Species of concern’’ or
‘‘Species of greatest conservation need.’’
Each State categorizes species under
these designations based on available
information about the status,
distribution, and trend of the species in
their State. They are not regulatory
classifications, but rather are intended
to guide resource managers in making
proactive decisions regarding species
conservation and data collection
priorities. The State Plans are not
intended to be specific action plans for
any species. These designations do not
result in any protection for the species.
However, the mountain plover is
identified as threatened in the State of
Nebraska, the only State where the
species is listed as endangered or
threatened.
Breeding Range
Colorado
In Eastern Colorado, the shortgrass
prairie ecosystem provides flat, dry
breeding habitat for the mountain
plover. The species occupies grasslands
within prairie dog colonies, grasslands
without prairie dog colonies, and dry
land agricultural fields (Dreitz et al.
2005, pp. 129–130; Tipton et al. 2009,
p. 496).
Knopf and Miller (1994, p. 504) noted
the PNG, Weld County, Colorado, as a
breeding stronghold for the species, but
in the mid-1990s the population fell
dramatically. The PNG now supports
relatively few breeding mountain
plover. In 2009, Knopf provided an
overview of mountain plover studies on
the PNG from 1986 through 2007. He
suggested that mountain plover
numbers on the PNG had been in
decline since the late 1930s and early
1940s, and that the dramatic decline in
the mid-1990s was the abrupt endpoint
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of a process of deteriorating habitat,
exacerbated by other factors such as wet
spring weather, increased predation,
and the relocation of breeding mountain
plover to better habitats elsewhere
(Knopf 2008, p. 61).
Despite the virtual loss of the PNG
population, over half of all mountain
plover are thought to breed in Colorado
(Andres and Stone 2009, p. 15). A recent
study reported a conservative estimate
of 8,577 breeding mountain plover in
eastern Colorado (95 percent CI 7,511 to
35,130) (Tipton et al. 2009, p. 497). A
separate, higher elevation population in
South Park, Park County, Colorado, was
estimated at 2,310 adults (Wunder et al.
2003, p. 661). Surveys through 2006
suggested a stable population in South
Park, with any variation largely
attributable to wet years and dry years
affecting breeding conditions (Wunder
2010a). Small numbers of mountain
plover also occur in Colorado’s San Luis
Valley (Hicks-Anderson and
VerCauteren 2006, entire). Andres and
Stone (2009, p. 8) provided population
estimates for the United States,
Canadian provinces, and Mexican States
based on their review of all available
information. Their estimate of 11,000
mountain plover breeding in Colorado
appears appropriate given information
available.
The BBS data from Colorado, 1966
through 2009 (¥0.9 percent decline
annually, 95 percent CI (¥7.0 to 3.5))
and 1999 through 2009 (0.3 percent
increase annually, 95 percent CI (¥5.5
to 14.7)) (Sauer 2010a), suggest little
long-term or recent change in breeding
numbers in Colorado. Based on these
data, we conclude that the current
breeding population in Colorado, which
likely supports half or more of all
breeding mountain plover, is relatively
stable.
Wyoming
Wyoming has the highest estimated
number of breeding mountain plover
outside of Colorado. The mountain
plover is locally common and has been
detected in every county of Wyoming
(Smith and Keinath 2004, p. 3). A
projected 20.5 million ac (8.3 million
ha) of mountain plover habitat exists in
Wyoming, with 59 percent occurring on
public lands (Wyoming Natural
Diversity Database (WYNDD) 2010;
Emmerich 2010).
Nesting of mountain plover in
Wyoming occurs in both grassland,
mostly in the eastern part of the State,
and desert-shrub (Plumb et al. 2005b, p.
20). Mountain plover densities were
comparable across habitat types with
overall density only slightly higher in
grassland than in desert-shrub (Plumb et
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al. 2005b, p. 20). Mountain plover
appear to have less association with
prairie dog habitat in Wyoming than
elsewhere (Plumb et al. 2005a, p. 226).
Little of the mountain plover breeding
range in Wyoming (approximately 12
percent) is on cropland Knopf and
Rupert 1999, p. 85).
Plumb et al. (2005b, pp. 19–20)
estimated a minimum population of
3,393 mountain plover in Wyoming in
2002 and 2003. Andres and Stone (2009,
p. 8) provide an estimate of 3,400
mountain plover breeding in Wyoming.
This number is based on Plumb et al.’s
estimate and, like that estimate, it
reflects the minimum number likely
present. Given that Plumb et al. (2005b,
pp. 19–20) provided a conservative
estimate, the actual breeding population
is likely larger; however, we have no
basis to provide a more accurate
estimate.
The BBS data from Wyoming (Sauer
2010a), 1966 through 2009 (¥1.2
percent decline annually, 95 percent CI
(¥5.7 to 3.3)) and 1999 through 2009
(¥2.3 percent decline annually, 95
percent CI ¥13.9 to 4.5)), suggest that
both long-term and recent declines in
breeding mountain plover numbers in
Wyoming may have occurred.
Montana
Primary breeding habitat for mountain
plover in Montana is in the northcentral portion of the State where
mountain plover are highly dependent
on black-tailed prairie dog colonies for
habitat. Montana Fish, Wildlife and
Parks modeled suitable mountain plover
habitat in the State. Mapping indicated
that the greatest area of highly suitable
habitat occurs in Phillips, Blain, Valley,
and Fergus Counties with patchy
distribution though the central and
southeast portions of the State. The total
area of suitable habitat estimated was
18.5 million ac (7.5 million ha)
(McDonald 2010).
Childers and Dinsmore (2008, p. 706)
reported an estimate of 1,028 mountain
plover in Phillips and Valley Counties
in 2004 (95 percent CI (903 to 1,153)).
In 2010, standardized census areas in
southwest, central, and northeast
Montana produced fewer sightings than
previous surveys (1992–2000, 2004);
however, McDonald (2010) stated that
results were negatively influenced by
above average rainfall, increased
vegetation height, and limited private
land access; therefore, results cannot be
relied upon. Other than apparent
confirmation of a previously
documented decline in the southwest
census area (FaunaWest Wildlife
Consultants 2004, pp. 4–5), no trends
could be inferred from the 2010 survey.
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Andres and Stone (2009, p. 8) used
the above estimate by Childers and
Dinsmore (2008, p. 706) and previous
estimates of about 600 mountain plover
elsewhere in Montana and provided a
Statewide estimate of approximately
1,600 mountain plover. BBS
observations of mountain plover on
routes in Montana were insufficient to
provide estimates of population trend.
New Mexico
Most breeding season reports of
mountain plover in New Mexico have
come from the northeast and western
counties. Sager (1996, pp. 8–9) found
152 presumed breeding adults at 35
sites in 11 counties in northern New
Mexico. Marguilies et al. (2004, p. 3)
estimated 200 mountain plover in
Union County alone throughout the
summer and located 46 nests. In a
limited effort, they also found 22
mountain plover and six nests on public
lands in Taos and Colfax Counties.
At BLM’s North Unit, Taos County,
point counts in 2005 through 2007
estimated 176 mountain plover on 8,400
ac (3,400 ha) of the 50,000-ac (20,000ha) unit considered to be favorable
mountain plover breeding habitat, based
on past observation of mountain plover
(Hawks Aloft 2007, pp. 9–11). If the
entire unit was occupied at the same
density, an estimated 1,000 mountain
plover might have been present on the
North Unit. Manderson (2010, pers.
comm.) inspected habitat away from
survey routes in 2010, and suggested
that, based on habitat quality, 500 or
more mountain plover could be present
on the entire unit. Mountain plover
numbers seen on the same survey routes
in 2010 were comparable to those in
earlier (2005 through 2007) surveys
(Hawks Aloft 2010, p. 13), suggesting
this population may be stable.
Goguen (2010, pers. comm.) estimated
a minimum of 40 to 50 breeding
mountain plover on the Vermejo Ranch,
Colfax and Taos Counties. Mountain
plover were also recently reported
present in El Malpais National
Conservation Area, Cibola County
(Hawks Aloft 2008, entire).
We found no Statewide breeding
surveys or estimates of Statewide
breeding populations for mountain
plover in New Mexico, other than
Andres and Stone’s (2009, p. 8)
conservative estimate of 500. Given the
above data from Union County, the
BLM’s North Unit in Taos County, the
Vermejo Ranch in Colfax and Taos
Counties, and likely mountain plover
occurrence in several other counties, we
believe that at least 1,000 and
potentially significantly more mountain
plover breed in New Mexico.
BBS data from New Mexico (Sauer
2010a), 1966 through 2009 (¥5.0
percent decline annually, 95 percent CI
(¥8.6 to ¥1.2)) and 1999 through 2009
(¥4.8 decline annually, 95 percent CI
(¥12.1 to 2.7)), demonstrate a long-term
decline and also suggest a short-term
decline in breeding mountain plover
numbers in New Mexico. New Mexico
is the only State for which the long-term
BBS trend statistically differs from zero.
Nebraska
In our December 5, 2002, proposal to
list the mountain plover we estimated
200 mountain plover in Nebraska (67 FR
72399). Recent studies attempted to
identify the extent of breeding
distribution and population size in
Nebraska (Bly et al. 2008, entire). Most
nests were found on agricultural fields
in Kimball County, in extreme
southwestern Nebraska, but mountain
plover were also found in nearby
Cheyenne and Blain Counties. The
minimum breeding population was
estimated to be 80 adults in 2007, based
on nests found, and the total estimate of
breeding birds ranged upward to 360
(Bly et al. 2008, p. 127). Van der Burg
et al. (2010, pp. 50–53) reported on
monitoring in the same three counties
(Kimball, Cheyenne, and Blain) in
southwestern Nebraska and estimated
that mountain plover breeding numbers
of 1,650, 1,617, and 1,558 over 3 years
of the study (2005, 2006, and 2007,
respectively). The authors attributed
past low estimates in Nebraska to:
(1) Low detection probabilities;
(2) clumped spatial distribution of
mountain plover, which their estimation
methodology corrected for; and (3)
‘‘chronic undersampling.’’ Given the
above estimates from Van der Burg et al.
(2010, pp. 50–53), an estimate by
Andres and Stone (2009, p. 8) of 500
breeding mountain plover in Nebraska
appears low.
Nebraska is the only State that has
regulatory mechanisms in place to
conserve the mountain plover and its
habitat, which likely protect relatively
few individuals. The Nebraska Game
and Parks Commission lists the
mountain plover as a ‘‘threatened’’
species. Listing of endangered and
threatened species identifies those
animals and plants whose continued
existence in Nebraska is in jeopardy.
Efforts can then be made to restore the
species or to prevent extirpation or
extinction. Once a species is listed, a
State law, titled the Nebraska Nongame
and Endangered Species Conservation
Act, automatically prohibits take,
exportation, and possession, and
imposes severe penalties on violators
(Nebraska Game and Parks Commission
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2011). Proposed projects that would be
authorized, funded, or carried out by
Nebraska State agencies are reviewed as
part of a mandatory consultation
process designed to prevent a State
action from jeopardizing the existence
of an endangered or threatened species.
Recovery plans for endangered or
threatened species are developed; these
recovery plans identify, describe, and
schedule the actions necessary to restore
populations of these animals and plants
to a more secure status. Given that most
mountain plover in Nebraska occur on
private agricultural lands, there are not
many State projects that are reviewed
under the law. It is generally
implemented only 4 or 5 times per year,
primarily on transportation,
transmission, and energy development
projects (Lackey 2011, pers. comm.).
While this law may provide protection
for some individual mountain plover in
Nebraska, we believe that it would only
have minimal positive effects on the
entire population in Nebraska, or on the
rangewide population.
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Oklahoma
Recent studies to determine the
breeding distribution and population
size in Oklahoma detected mountain
plover in Cimarron and Texas Counties
in the Oklahoma panhandle, mostly on
fallow or barren agricultural fields
(McConnell et al. 2009, pp. 30–33).
Randomized point counts were used to
derive a Statewide population estimate
of 68 to 91 birds (McConnell et al. 2009,
pp. 32–33). Andres and Stone (2009, p.
8) estimated 200 mountain plover
breeding in Oklahoma. Given results of
McConnell et al. (2009, pp. 32–33), we
believe that Andres and Stone’s (2009,
p. 8) estimate may be slightly high. The
range of the mountain plover in
Oklahoma was described as stable over
the past 100 years, with the suggestion
that populations may have changed
little (Hatcher 2010).
Kansas
The Kansas Department of Wildlife
and Parks (2005) stated that mountain
plover breed only on dry upland in the
shortgrass prairie of western Kansas.
While conversion to agriculture has left
little native breeding habitat, Cable and
Seltman (2010, pp. 50–51) reported
mountain plover are an uncommon but
regular breeding species in western
Kansas and that they also use idle
cropland. Morton County may also serve
as a staging area for migration in late
summer (Cable and Seltman 2010, p.
51). Andres and Stone (2009, p. 8)
estimated 200 breeding mountain plover
in Kansas. No comprehensive surveys of
breeding mountain plover in Kansas
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have been attempted; however, given
their apparent use of both prairie and
cropland, and a substantial population
in nearby Colorado, the estimate may be
appropriate.
Texas
The mountain plover likely breeds in
Texas, but there are no confirmed
reports of breeding since 1993 (Andres
and Stone 2009, p. 16). Holliday (2010)
described breeding season sight reports
of mountain plover from the Texas
Panhandle near known Oklahoma
breeding sites. Holliday (2004) also
mapped potential breeding habitat,
much of it on private land that has not
been surveyed. Andres and Stone (2010)
did not provide an estimate of breeding
mountain plover in Texas. We believe
that at least minimal numbers of
mountain plover breed in Texas.
Arizona
The only known mountain plover
nesting in Arizona is in Apache County
in east-central portion of the State, with
at maximum perhaps a dozen breeding
birds (Gardner 2010, pers. comm.).
Breeding has occurred on grasslands
where cattle were concentrated and at
Gunnison prairie dog (C. gunnisoni)
colonies (Corman 2005, pp. 591–591;
Gardner 2010). However, hundreds of
square miles of potential breeding
habitat in northern and western Arizona
have never been surveyed, and there are
reports of potential breeding mountain
plover on Tribal lands in Navajo County
(Corman 2005, pp. 591–591; Gardner
2010, pers. comm.). Andres and Stone
(2009, p. 8) estimated 100 breeding
mountain plover in Arizona. This
estimate acknowledges potential for a
more substantial breeding population
than limited observations have
documented.
Utah
The mountain plover has been a
historically rare breeder in shrub-steppe
habitat in the Uinta Basin of
northeastern Utah. Manning and White
(2001, p. 225) described a small
breeding population that averaged about
15 adults yearly. Mountain plover
breeding in the area subsequently
declined, and no birds have been found
during surveys of the area since 2003
(Maxfield 2010, pers. comm.). Andres
and Stone (2009, p. 8) estimated fewer
than 50 breeding mountain plover in
Utah. Based on no recent records of
breeding mountain plover, this estimate
may be optimistic.
North Dakota and South Dakota
The mountain plover once bred in
these States, with higher numbers
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present in South Dakota, but there are
no recent breeding records in either
North Dakota or South Dakota (North
Dakota Game and Fish Department
2010; South Dakota Game, Fish and
Parks 2010).
Canada
A review of breeding records for
Canada (Knapton et al. 2006, p. 33)
concluded that the mountain plover is
a peripheral species in Canada with no
evidence that it was ever a common or
regular breeder. The first breeding
record was documented in 1979 and the
most recent in 2007 (Knapton et al.
2006, pp. 32–33; Holroyd 2010, pers.
comm.). Most sightings and breeding
records come from extreme southeastern
Alberta, with at least one incidence of
confirmed breeding in Saskatchewan.
Holroyd (2010, pers. comm.) provided
updated records of sightings through
2009, mostly from Alberta. Andres and
Stone (2009, p. 8) estimated fewer than
100 mountain plover breeding in
Canada. We are not aware of any
attempts to systematically survey all
potential breeding areas in the Canadian
range. However, given the low number
and limited distribution of reported
recent sightings (Holroyd 2010, pers.
comm.), we believe that actual breeding
numbers are fewer than 100.
Mexico
Breeding records of mountain plover
in Mexico have been documented in
southeastern Coahuila and Nuevo Leon,
following a history of breeding season
observations in Mexican prairie dog
colonies (Desmond and Chavez-Ramirez
2002 entire; Gonzalez-Rojas 2006, pp.
81–84). Nesting is suspected in San Luis
Potosi, 130 mi (200 km) south of the
above records (Luevano et al. 2010, p.
123).
The extent of mountain plover
breeding in Mexico is largely unknown.
Andres and Stone (2009, pp. 8, 15)
estimated fewer than 300 mountain
plover breeding in Mexico (fewer than:
50 in Chihuahua, 100 in Cohuila, 100 in
Nuevo Leon, and 50 in San Luis Potosi),
but suspect that if there are major
concentrations of breeding mountain
plover not yet discovered anywhere in
their range, they are likely in Mexico.
The estimate of fewer than 300 birds is
at best a guess, but is appropriately
conservative given the lack of
knowledge regarding breeding mountain
plover occurrence and distribution in
Mexico.
In summary, we believe that the
rangewide breeding population of
mountain plover likely exceeds 20,000,
with largest populations in Colorado,
conservatively 11,000; Wyoming,
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conservatively 3,400; Montana 1,600;
Nebraska 1,600; New Mexico, at least
1,000 and potentially many more; and
smaller populations elsewhere (Kansas,
Oklahoma, Texas, Utah, Canada, and
Mexico).
Wintering Range
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California
Mountain plover are found from
north-central California to the Mexico
border, mostly from September to midMarch, with peak numbers from
December through February (Knopf and
Wunder 2006; Hunting and Edson 2008,
p. 181). Mountain plover were
historically common on the coastal
plain in southern California (coastal
prairie, alkaline flats, agricultural fields)
before being displaced by human
development (Hunting and Edson 2008,
p. 182; Wunder and Knopf 2003, p. 78).
Historically, much of the mountain
plover habitat in the Central Valley
grasslands was lost following the
decline of grazing elk (Cervus
canadensis), pronghorn antelope,
burrowing kangaroo rats, ground
squirrels (Spermophilus spp.), and other
mammals. The combined activities of
these herbivores maintained suitable
habitat conditions for mountain plover,
conditions closely resembling habitat
characteristics found on breeding
habitats (Knopf and Rupert 1995, p.
750). Farther south in California, desert
scrub in the Imperial Valley was
converted to agriculture beginning in
the 1940s, creating important wintering
habitat for the mountain plover. See
Hunting and Edson (2008, p. 181) for
details of the mountain plover’s
historical range and abundance in
California.
Mountain plover currently occur in
the greatest numbers in two general
areas in California: (1) The western
Central Valley from southern Colusa
and Yolo Counties in the north to Kern
County in the south (especially the
western San Joaquin Valley, the name
by which the southern Central Valley is
known); and (2) the Imperial Valley in
Imperial County (Hunting and Edson
2008, p. 182). The Carrizo Plain,
separated from the San Joaquin Valley
by the Temblor Range, and the Panoche
Valley are also regularly occupied
wintering areas.
Populations and trends in the Central
Valley are difficult to determine due to
the abundance of potential habitat, flock
movements, and lack of systematic
surveys (Knopf and Rupert 1995, p. 749;
Edson and Hunting 1999, p. 17). In our
December 5, 2002, proposal to list the
mountain plover (67 FR 72396), we
included Edson and Hunting’s 1999 (p.
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27) comment that mountain plover were
‘‘rare and local, exceedingly rare, or
accidental’’ within individual counties
in the San Joaquin Valley. Wunder and
Knopf (2003, p. 78) suggested that, as a
result of habitat loss, many mountain
plover had shifted from the Central
Valley to the Imperial Valley. Hunting
and Edson (2008, p. 182) considered
reports of 200 to 300 birds in the San
Joaquin Valley in winter of 2004–2005,
100 to 200 in Madera County in 2005–
2006, 645 in Tulare County in December
2005, and about 300 in western Kings
County in January 2006 to be
‘‘exceptional.’’ They also found
noteworthy a survey total of 381
mountain plover at the Carrizo Plain in
2006 (Hunting and Edson 2008, p. 182).
However, recent reports from the
Central Valley also include 645 birds in
Madera County in 2006 (McCaski and
Garrett 2006, p. 283), 426 in Tulare
County in 2007 (McCaski and Garrett
2007, p. 326), 230 in San Joaquin
County in 2008 (eBird 2010), 230 in
Solano County in 2008 (Central Valley
Bird Club 2010), and 223 in Kern
County in 2010 (eBird 2010). These
reports suggest that significant numbers
of mountain plover continue to use
widespread areas of the Central Valley
annually. Nearby, a recent high count
for the Carrizo Plain National
Monument was 540 birds in 2009
(Sharum 2010).
In the Imperial Valley, coordinated
surveys by 26 observers over 2 days in
December 1999 sighted 3,758 mountain
plover (Shuford et al. 2004, p. 7). A
survey of mountain plover and their use
of cultivated fields in the Imperial
Valley of California in 2001 found 4,037
birds (Wunder and Knopf 2003, p. 75),
and 3,476 were counted from January 29
through February 6, 2002, by four
observers, with the largest flock
consisting of 410 birds (AMEC Earth
and Environment 2003, p. 9–10).
Mountain plover wintering in the
Imperial Valley were surveyed in 2003
and 2004, in an attempt to develop a
statistically reliable estimate of numbers
(Knopf and Wunder 2004, entire).
Flocking behavior, mobility, and
weather were among factors found to
limit the reliability of Imperial Valley
estimates (Knopf and Wunder 2004, pp.
9–12). Results of more recent survey
estimates in the Imperial Valley include
more than 4,500 mountain plover seen
in January 2007, approximately 3,000
seen in January 2008, and 827 seen in
January 2011 (Kelsey 2011, pers.
comm.).
Hunting et al. (2001 p. 40), Wunder
and Knopf (2003, p. 76), and Hunting
and Edson (2008, pp. 181–183) all
suggested a significant decline in
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numbers of mountain plover wintering
in California over previous decades.
However, we found little evidence
available to establish any trend in more
recent (2000 to present) wintering
numbers in California. The 4,500
mountain plover recorded in the
Imperial Valley survey in 2007 (Kelsey
2011, pers. comm.) exceeded mountain
plover observed in Statewide surveys
from 1994, and 1998 through 2002
(Knopf 1996, p. 12; 68 FR 53083). Most
recently, a Statewide survey over 5 days
in January 2011 found 1,235 mountain
plover (Kelsey 2011, pers. comm.),
considerably fewer than found in
previous Statewide surveys or recent
Imperial Valley surveys. However, it is
not apparent how unusually wet
weather or other factors contributed to
the relatively low number of mountain
plover reported in the 2011 survey.
California experienced heavy rains in
late 2010. December 2010 was the City
of Los Angeles’ wettest December in 121
years (Southern California Weather
Notes 2010).
While California remains the best
documented wintering area for the
mountain plover, it may winter less
than 50 percent of the estimated
breeding population (Andres and Stone,
p. 9). Knopf (1996, p. 12) estimated
7,000 mountain plover wintering in
California and 1,000 to 3,000 wintering
elsewhere. In our December 5, 2002,
proposed rule to list the mountain
plover as threatened, we suggested that
few mountain plover wintered in Texas,
Arizona, and Mexico (67 FR 72397). We
do not know the actual number of
mountain plover wintering in California
or how the number varies from year to
year; however, given no recent evidence
that wintering birds in California
number more than the 7,000 estimate
above (Knopf 1996, p. 12), and our
current rangewide estimate of at least
20,000 breeding mountain plover, the
previous contention that California
winters the majority of all mountain
plover appears incorrect. The fewer
mountain plover that are wintering in
California, on average or in any given
winter, the more important that
wintering areas outside California
become. Unfortunately, we have little
information to pinpoint where the
majority of mountain plover are
wintering.
Texas
Holiday (2010), based on an
examination of LandSat (satellite)
photos, found that winter records of
mountain plover in Texas correlated to
the distribution of barren fields and
grazed pastures. He also suggested that
the northern limit of the wintering range
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in Texas is related to the average
number of frost-free days, which
influences insect availability. Collins
(2006, pp. 27–31) summarized mountain
plover wintering status in Texas (with
much of the compiled records and maps
attributable to Holliday). Populations in
Hondo County and Medina County
areas were described as potentially the
largest; Williamson County was
characterized as a well-known wintering
area, but with populations potentially
small compared to other less known
areas. Mountain plover were also
present around Wharton, Wharton
County, and surrounding counties, and
the Corpus Christi area was said to
potentially hold more mountain plover
than reports indicate (Collins 2006, p.
30). Estimates by knowledgeable local
birders of wintering mountain plover in
the coastal bend area (Nueces and San
Patricio Counties) ranged from 200 up to
2,000 to 3,000 birds (Cobb 2009, pers.
comm.). The higher numbers were
characterized as speculative because the
vast amount of available habitat where
access is generally limited makes it
difficult to draw any conclusions.
Andres and Stone (2009, p. 20) provided
an estimate of 1,500 mountain plover
wintering in Texas, with a note that
abundance could be much greater.
Arizona
Approximately 500 mountain plover
are believed to winter in agricultural
areas of southern and western Arizona,
but numbers could be higher because
private and Tribal lands are largely
unsurveyed (Gardner 2010). Wintering
numbers in La Paz and Pinal Counties
appeared stable; numbers in Cochise
County have significantly decreased in
the last 10 to 15 years due to urban
expansion; and Yuma County
populations were characterized as
increasing, with 150 to 300 birds
annually (Gardner 2010; Robertson
2010, pp. 3–4). Wintering mountain
plover are also reported from the
Sulphur Springs Valley in Cochise
County (Robertson 2010, p. 2). Andres
and Stone (2009, p. 20) provided an
estimate of 200 mountain plover
wintering in Arizona. Given limited
coverage of potential wintering habitat,
we consider the above estimate of 500
birds wintering in Arizona the likely
minimum.
Nevada
Wintering mountain plover are rarely
reported from Nevada, with the most
recent reports of up to 17 mountain
plover coming from the Armagosa
Valley near the Nevada-California
border northwest of Las Vegas (eBird
2010).
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New Mexico
While some mountain plover likely
winter in southern New Mexico, we
have no information regarding locations
or numbers.
Mexico
Mountain plover’s winter distribution
in Mexico has not been well studied,
but the species is believed to winter
from along the United States-Mexico
border south into the border States of
Baja California, Sonora, Chihuahua,
Coahuila, Nuevo Leon, and Tamaulipas,
and beyond into Durango, Zacatecas,
and San Luis Potosi (Gonzales-Rojas et
al. 2006, p. 81; Knopf and Wuder 2006;
Macias-Duarte and Punjabi 2010, p. 4).
While the Mexicali Valley, Baja
California, located just south of the
Imperial Valley, seems to have suitable
wintering habitat (200,000 ac (80,000
ha) of farmland), mountain plover have
rarely been reported from the area
(Macias-Duarte and Punjabi 2010, p. 3).
Two primary concentration areas
within the Chihuahuan Desert are
believed to be most important for
wintering mountain plover: (1) The
Janos area in northwestern Chihuahua;
and (2) the El Tokio grasslands in
southern Coahuila, Nuevo Leon,
northeastern Zacatecas, and northern
San Luis Potosi (Macias-Duatre and
Punjabi 2010, pp. 3–6). Mountain plover
are most abundant in the La Soledad
region of the El Tokio grasslands. The
highest estimated density in Llano de la
Soledad (based on data from the winter
of 2005–2006) extrapolated over the area
suggests that over 2,000 mountain
plover were present. Extrapolation from
Llano de la Soledad to all prairie dog
colonies in the entire El Tokio region
provided an estimate of 6,800 mountain
plover (Macias-Duarte and Punjabi
2010, p. 6). While this estimate is crude
and may be optimistically high, it is not
inconsistent with reports of mountain
plover flocks in the area totaling 1,600
to 3,500 birds reported by Andres and
Stone (2009, p. 18). In the winter of
2005–2006, surveys in Janos estimated
1,435 birds (Salinas 2006, p. 43).
The reported sightings and the
estimates presented above are
maximums reported, and the numbers
can vary greatly from year to year.
However, these reports suggest that a
substantial number of mountain plover
may winter in Mexico. Andres and
Stone (2009, p. 20) provided an estimate
of 5,000 birds wintering in Mexico.
Changes in sampling methodology,
annual variability in mountain plover
numbers, and the short duration
covered by recent systematic surveys
prevent any conclusions regarding
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trends (Macias-Duarte and Punjabi 2010,
pp. 5–6, 16, 17).
Summary of Comments and
Recommendations
We requested written comments from
the public on the proposed listing of the
mountain plover during the June 29,
2010, through August 30, 2010,
comment period that followed our June
29, 2010, document (75 FR 37353)
vacating our September 9, 2003,
withdrawal (68 FR 53083) and
reinstating our December 5, 2002,
proposal to list the mountain plover (67
FR 72396). We contacted appropriate
Federal, State, and local agencies;
scientific organizations; and other
interested parties, and invited them to
comment on the proposed rule and
supporting documents. Following an
initial draft of our final determination
we contacted 5 peer reviewers and
asked them to review selected portions
of the draft.
We received 53 comments in response
to the December 5, 2002, proposed rule
(67 FR 72396) during the June 29, 2010,
to August 30, 2010, comment period.
These included comments from 3
Federal entities, 10 States, 3 local
governments, 28 organizations or groups
(business, industry, environmental), and
8 private parties. WildEarth Guardians
also forwarded us 302 similar comments
from individuals, and the Colorado
Farm Bureau forwarded us 8 similar
comments from individuals. We
received no requests for public hearings.
We also reviewed comments received
after our February 16, 1999, and
December 5, 2002, proposals to list the
mountain plover (64 FR 7587 and 67 FR
72396, respectively) for relevant issues
not addressed in more recent comments.
All substantive comments have either
been incorporated into this final
determination or are addressed below.
Peer Review
In accordance with our policy
published in the Federal Register on
July 1, 1994 (59 FR 34270), we solicited
expert opinions from five
knowledgeable individuals with
scientific expertise that included
familiarity with the mountain plover,
with other shorebird species, the
geographic region and habitats in which
the mountain plover occurs, and
conservation biology principles. We
provided reviewers with a partial draft
of this document. We received
responses from all five of the peer
reviewers that we contacted. The peer
reviewers generally agreed that we
accurately described the species and its
habitat requirements; that we provided
accurate review and analysis of factors
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affecting the species; that our
assumptions and definitions of suitable
habitat were logical and adequate; that
there were few oversights, omissions, or
inconsistencies in out draft document;
and that we used pertinent literature to
support our assumptions and
conclusions. One reviewer was
generally critical of the synthesis of
information regarding threats to
mountain plover habitat, especially our
assessment of wintering habitat in the
Imperial Valley. One reviewer limited
comments primarily to population
trends. The peer reviewers provided
suggestions to improve this final
document. Recommended editorial
revisions, clarifications, and other
changes have been incorporated into the
final document as appropriate. We
respond to all substantive comments
below or through changes to the final
document.
Comments From Peer Reviewers
(1) Comment: Three reviewers
questioned specific details of our range
map.
Our Response: Figure 1, depicting the
mountain plover’s range, was developed
based on those in Knopf and Wunder
2006, and Andres and Stone 2009, with
modifications based on our review of
recent information. Our map depicts
generalized areas believed to support
breeding and wintering mountain
plover, and does not depict localized
areas of presence or absence. We made
some revisions to our range map based
on reviewer comments.
(2) Comment: One reviewer pointed
out that while mountain plover are
attracted to burned areas on their
breeding ground, there is little evidence
as to whether such burned areas benefit
breeding mountain plover (for example,
through higher nest success or fledging
success) compared to habitats they may
otherwise use.
Our Response: Reduced vegetative
cover resulting from burning appears
more attractive to mountain plover than
similar habitat left unburned. However,
we agree that studies have not
documented the specific relationship of
burning to successful mountain plover
nesting.
(3) Comment: One reviewer stated
that estimates of annual survival should
be considered minimum estimates,
because studies do not control for
permanent migration of mountain
plover (i.e., they assume birds not
accounted for have died rather than
moved away from the study area).
Our Response: We agree and have
acknowledged this in the text. Studies
in Montana have produced the most
complete information on juvenile (first
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year of life) and adult mountain plover
annual survival rates, but the extent to
which these studies underestimate
survival rates due to emigration is not
known.
(4) Comment: One reviewer asserted
that recent literature clearly identified
adult survival as a vital importance to
productivity and survival of shorebird
populations.
Our Response: We agree. In the
limited studies that have estimated
adult survival of mountain plover, adult
mountain plover survival appears
relatively high. The suggestion that
management efforts to increase
mountain plover populations might best
be targeted at increased chick survival
(hatching to fledging) result, in part,
from data showing relatively low and
highly variable survival of mountain
plover chicks (see Survival, Lifespan,
and Site Fidelity above).
(5) Comment: Two reviewers noted
that while the mountain plover may
have a long lifespan compared to many
other shorebirds, some shorebirds do
live longer and other bird families, such
as seabirds, live much longer.
Our Response: Mountain plover in the
wild have been known to live to over 10
years. We have qualified our description
of the mountain plover as a ‘‘relatively’’
long-lived species.
(6) Comment: One reviewer suggested
that mountain plover fidelity to
breeding sites is more regional than sitespecific and that differences in habitat
across the mountain plover breeding
range may influence site fidelity.
Our Response: Both may be correct.
Lack of genetic differentiation found by
Oyler-McCance et al. (2005, p. 359;
2008, pp. 496–497) suggest that mixing
of mountain plover across regions is
also occurring.
(7) Comment: One reviewer suggested
that we discuss spatial and temporal
variation in long-term and recent BBS
trend data for the mountain plover and
cited a long-term (1966 through 2009),
negative New Mexico trend as the only
statistically significant population trend
among the rangewide or Statewide BBS
trend estimates we provide.
Our Response: We have included data
pertinent to spatial and temporal (by
State and long-term versus short-term)
trends in mountain plover populations
in this document when available (see
Conservation Status and Local
Populations above). These statistics are
based on fewer data and generally
appear less reliable than rangewide
trends. The long-term trend estimate in
New Mexico is unique among those we
cite, in that it reflects a statistically
significant indication of at least some
decline.
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(8) Comment: One peer reviewer
stated that there is insufficient
information about the distribution and
status of the mountain plover in Mexico
to evaluate whether past, present, or
future loss of prairie dogs and the
ecosystem they support in Mexico is a
significant threat to the mountain
plover.
Our Response: We agree that
information on the distribution and
status of the mountain plover in Mexico
is limited. Based on the information
available, past loss of prairie dogs
colonies in Mexico has decreased
available mountain plover habitat and
may have had some adverse impact on
the mountain plover. Recent Mexican
and international attention to
conservation of prairie dogs and
grassland complexes in Mexico
improves prospects for maintaining
existing mountain plover wintering
habitat (see Factor A below). While
future losses of prairie dog colonies in
Mexico may occur, we do not believe
that associated impacts to mountain
plover’s habitat present a significant
threat to the mountain plover over its
wintering range.
(9) Comment: One reviewer stated
that discussion of habitat loss to land
use modification would be greatly
improved by including specifics of how
these losses fall within the precise
breeding and wintering habitats of the
mountain plover. Two reviewers
contended that the relative threat posed
by agricultural conversion (of
grasslands) was difficult to assess unless
analyzed at a fine spatial scale.
Our Response: The mountain plover’s
breeding and wintering ranges extend
across a large area and encompass a
variety of habitat types. We have
addressed habitats supporting the
mountain plover, habitat losses, and
threats to mountain plover habitat on a
rangewide and regional level, and in
some cases on a State or local level as
well.
(10) Comment: One reviewer offered
that uncertainties regarding future
agricultural practices on private lands
emphasized the importance of managing
for the mountain plover on State and
Federal lands.
Our Response: A great degree of
uncertainty exists regarding future
agricultural practices on private lands,
but we believe that changes in
agriculture are not likely to significantly
threaten the mountain plover in the
foreseeable future. Across the range of
the mountain plover there are currently
many initiatives, on both public and
private lands, to manage habitat for
wildlife including the mountain plover,
bird species using similar habitats, and
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prairie dogs (see Factor A discussion
below). The mountain plover has been
designated a bird of conservation
concern by the Service (2008) and has
special conservation status in many
States (see Conservation Status and
Local Populations above and Factor A
discussion below). We anticipate and
support continued emphasis on
mountain plover conservation and
management by our Federal and State
partners.
(11) Comment: One reviewer noted
that, without synthesis of exactly what
agricultural lands mountain plover
require on their wintering areas and
how those specific fields are threatened
(for example, fallowing of crop fields in
California’s Imperial Valley), our
conclusion that threats impacting only a
small portion of agricultural lands
would not affect mountain plover was
problematic.
Our Response: In Migration and
Wintering Habitat above, we describe
wintering habitats favored by the
mountain plover. In Factor A below we
discuss threats that may impact these
habitats, including threats to certain
crop types favored by the mountain
plover. The level of analysis we provide
is sufficient to evaluate threats to the
mountain plover from changes on
agricultural lands that provide
wintering habitat and utilizes the best
available information we have regarding
this topic. Without specific information
to suggest otherwise, we conclude that
threats would not disproportionately
impact those particular fields that
presently receive, or in the future would
receive, most use by the mountain
plover.
(12) Comment: One reviewer noted
that the Imperial Valley, California, an
area supporting significant numbers of
wintering mountain plover, is one of the
fastest growing areas of the United
States.
Our Response: From 1984 to 2008,
urban area in the Imperial Valley
increased by 6,000 ac (2,400 ha) (CDC
2010), much of it outside of croplands
favored by the wintering mountain
plover. About 381,000 ac (154,000 ha) of
field crops are present in the Imperial
Valley (Imperial Irrigation District (IID)
2009a). We concluded that population
growth and urban expansion is having
a modest impact on Imperial Valley
croplands, but does not rise to the level
of a threat to the species (see Factor A
discussion below).
(13) Comment: One reviewer stated
that, over the wintering range of the
mountain plover, increase in human
population, associated land use
changes, and reductions in available
water for agriculture would impact areas
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currently used by mountain plover. The
reviewer concluded that because there
was ‘‘lack of suitable habitat to move to,’’
this would be detrimental to mountain
plover.
Our Response: Human development
and changes in agriculture, including
changes brought on by future water
availability, are likely to impact some of
the areas currently used by wintering
mountain plover in California, in
southern Arizona, and elsewhere in
their wintering range. Based on the
likely magnitude of such changes and
the extensive wintering range of the
mountain plover, we conclude that loss
of wintering habitat is not likely to be
a significant threat to the mountain
plover in the foreseeable future (see our
discussion in Factor A below).
(14) Comment: One reviewer
questioned whether mountain plover
are impacted by pesticides and
herbicides used on sod farms where
they are often seen during migration or
in winter.
Our Response: We have found no
documentation of effects to mountain
plover from exposure to pesticides on
sod farms. However, in the past, the use
of diazinon, an organo-phosphate
pesticide, on sod farms may have
impacted the mountain plover. In 1988,
after documented large die-offs of birds
of other species, the U.S. Environmental
Protection Agency (EPA) cancelled the
registration of diazinon for use on golf
courses and sod farms (EPA 2006, p.
vii). We have no information regarding
significant harm of any bird species
since 1988 that is attributable to use of
pesticides on sod farms.
(15) Comment: One reviewer
suggested more discussion on invasive
grasses and their impact on mountain
plover.
Our Response: Invasive plants,
including nonnative grasses planted as
forage for cattle, are widespread across
the western United States. Many
invasive plants grow to a density or
height that can make habitat unsuitable
for mountain plover. While perceived
by some as a potential threat, the effects
of nonnative grasses and invasive plants
on the mountain plover have not been
well documented. Within the
ecosystems it inhabits, the mountain
plover is best supported where native or
domestic herbivores, fire, dry
conditions, soil conditions, or
disturbance create low, sparse
vegetation. In general, this is true
whether the vegetative community
consists only of native vegetation or also
supports a component of nonnative or
invasive plants.
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Public Comments
Process Issues
(16) Comment: One commenter stated
that e-mails, personal communications,
and letters that the Service referenced in
support of the December 5, 2002, listing
proposal (67 FR 72396) do not meet the
best information available standard as
described in Service policy (59 FR
34271, July 1, 1994).
Our Response: Our policy, as cited
above, requires that we evaluate all
scientific and other information
available, which includes both
published and unpublished materials,
in the development of a listing action.
We review the information regardless of
origin, and determine whether it is
reliable, is credible, and represents the
best information available regarding the
species under review. We document our
evaluation of any information we use in
making our decision, whether it
supports the decision or not.
(17) Comment: Commenters believed
that our analysis in our February 16,
1999, and December 5, 2002, proposals
to list the mountain plover (64 FR 7587
and 67 FR 72396, respectively) used
‘‘selective science’’ to defend our
position, while ignoring information
contrary to our conclusion.
Our Response: We base our
determinations on review of all
pertinent information available. This
final determination is further based on
substantial new and additional
information available since our previous
actions.
(18) Comment: One commenter stated
that in the 1999 and 2002 proposals to
list the mountain plover (64 FR 7587
and 67 FR 72396, respectively) the
Service did not identify or quantify
actual threats, and therefore the Service
has not shown that mountain plover
have declined or are at risk.
Our Response: In this final
determination, we have evaluated the
relative security of the species from
present and foreseeable threats across its
breeding, migratory, and wintering
range. Where available information has
allowed, we have identified and
quantified actual threats to the
mountain plover in this evaluation.
While threats, especially future threats,
may be difficult to quantify, we evaluate
threats based on analysis of the best
scientific and commercial information
available.
(19) Comment: One commenter stated
that e-mails and faxes should be
accepted as comment on the proposed
listing.
Our Response: Our policy requires
submission of written comments
through the Internet (via the Federal
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eRulemaking Portal at https://
www.regulations.gov), or by U.S. mail or
hand-delivery, and we believe this
provides the means for all interested
parties to provide comments,
information, and recommendations.
(20) Comment: Various commenters
suggested that there are either more or
fewer reasons for listing the mountain
plover now compared to 2003 when our
proposed listing was withdrawn (68 FR
53083, September 9, 2003).
Our Response: Our 2003 decision was
vacated by the Court and is not relevant
to this final determination regarding the
mountain plover. We have based our
determination on the current status of
the mountain plover and current and
future threats to the species, based on
the best scientific and commercial
information available to us at this time.
Issues Regarding Range, Numbers, and
Populations Trends
(21) Comment: One commenter
questioned our emphasis on the PNG in
Colorado and Charles M. Russell
National Wildlife Refuge (NWR) in
Montana in our proposals to list the
mountain plover, as relatively few
mountain plover breed in either site.
Our Response: We agree that neither
site currently supports a large
percentage of the total mountain plover
population. Both sites are Federally
controlled and have supported
mountain plover research and
management efforts. The PNG once
likely supported the highest density of
mountain plover in the species’
breeding range. The dramatic loss of this
sizable population has relevance to the
rangewide population trend and may
provide insight to current and future
threats to the mountain plover. Charles
M. Russell NWR provides management
opportunities on a Montana site
representative of those where mountain
plover is largely dependent on the
black-tailed prairie dogs to create
desirable habitat conditions.
(22) Comment: One commenter stated
that breeding habitat on public and
private lands in the mountain plover’s
range has not been adequately surveyed
and suggested that additional surveys
will consistently find more mountain
plover.
Our Response: Knowledge of
mountain plover populations varies
greatly across the breeding range.
Surveys vary in methodology and scope.
In some cases, lack of access to conduct
surveys on private lands limits the
accuracy of population estimates. Based
on information available since 2002,
estimates of mountain plover breeding
numbers in certain States and
throughout the range have been
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modified. Former rangewide population
estimates were based on surveys of
mountain plover in California, where
the vast majority of birds were thought
to winter. Our current rangewide
population estimate is based on
minimum breeding range population
estimates. However, no estimate
currently exists that provides a precise
estimate of rangewide numbers.
(23) Comment: One commenter
dismissed population estimates as ‘‘just
a guess.’’
Our Response: We believe that some
structured studies on the breeding range
have produced population estimates
that approximate the actual numbers of
mountain plover that are present. In
other cases, estimates may be limited to
the minimum number of individuals
known, or may suggest the likely
population size based on limited data.
While we summarize population
estimates and seek to understand
population trends, numbers alone are
not the basis for listing determinations
under the Act. Listing determinations
are based on whether there are threats
present or likely to occur that would
result in the species being in danger of
extinction or likely to become so within
the foreseeable future.
(24) Comment: Several commenters
cited increased rangewide population
estimates as a reason why the mountain
plover does not merit listing. One
commenter cited the recent status
change by the IUCN (downlisting from
‘‘vulnerable’’ to ‘‘nearly threatened’’) as
evidence of reduced threat to the
species.
Our Response: While greater
abundance suggests less vulnerability,
we have no basis to suggest that the
increased estimate of mountain plover
numbers reflects an actual, rangewide
increase. The number of individuals of
a species present is only one factor
considered when assessing vulnerability
to extinction. Current and future threats
may be of greater significance.
Downlisting by the IUCN was based on
revised population estimates alone, and
not on changed interpretation of threats
present.
(25) Comment: One commenter noted
that all wintering areas in the United
States and Mexico have not been located
and opined that further searching is
likely to yield more wintering sites.
Our Response: While more
information overall has been gathered
since our 2002 proposal (67 FR 72396,
December 5, 2002), much is still
unknown regarding wintering habitat.
Rangewide breeding population
estimates and wintering estimates from
California suggest that a substantial
percentage of mountain plover winter
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elsewhere. Because the large flock sizes
observed in California are not regularly
encountered elsewhere, mountain
plover numbers may occur at lower
densities in other parts of their
wintering range.
(26) Comment: One commenter stated
that the former estimate of 20,000
breeding mountain plover at the PNG in
the 1970s may have been off by an order
of magnitude.
Our Response: While the actual
number present in the 1970s is
unknown, it is well established that
mountain plover populations on the
PNG have greatly decreased since that
time, with relatively few breeding
mountain plover present since the mid1990s.
(27) Comment: One commenter
questioned our estimates of up to 10,000
mountain plover at Kern NWR in
California during the 1960s.
Our Response: Many mountain plover
used Kern NWR in winter during the
1960s, but the 10,000 estimate is by far
the largest recorded (Engler 1992). We
believe estimates at Kern NWR
approximate mountain plover numbers
attracted to the refuge by favorable
habitat conditions previously present.
(28) Comment: Multiple commenters
mentioned continued, significant
declines across the breeding and
wintering range of the mountain plover,
as cited by researchers, as indicative of
the species’ imperiled status.
Our Response: Documentation of
historical range contraction and
apparent decline in mountain plover
populations is reflected in long-term
BBS and CBC trends. Despite more
intensive study in recent years, it is not
clear if, or to what extent, any declines
in mountain plover populations
continue. See our discussion of
Population Size and Trends above.
(29) Comment: A few commenters
stated that BBS and CBC data and trends
regarding mountain plover are
unreliable. Others state that these data
are a reason for concern.
Our Response: The BBS is the best
available long-term trend information
for the mountain plover on its breeding
range. It is an imprecise indicator of
mountain plover population trends.
These data appear to confirm a decline
over the period 1966 through 2009, but
results suggest that the rate of any
continued (1999 through 2009) decline
has moderated. The CBC data are more
restricted in geographic scope than are
the BBS data, but these data also suggest
a long-term decline. Few CBC count
circles regularly report mountain plover,
and numbers are highly variable, likely
reflecting mobility of wintering flocks.
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See our discussion of Population Size
and Trends above.
(30) Comment: We received a
comment that insufficient data are
available to predict any trend toward
extinction.
Our Response: We agree that current
trend data are limited and that the
ability to project future population
trends is difficult. However, we have
reviewed the best population and trend
data available as part of our analysis of
the mountain plover’s status. In making
our final listing determination, we not
only looked at population trends, but
we have also evaluated the best
available information on current and
future threats to the species.
(31) Comment: One commenter
suggested that population trends at the
PNG, where the birds have been closely
studied, are indicative of the overall
population trend for the mountain
plover.
Our Response: Knopf (2008, p. 61)
summarized mountain plover studies on
the PNG in Weld County, Colorado, and
suggested reasons for that population’s
former abundance and more recent
decline, including long-term changes in
habitat since abandonment of
agricultural fields following the ‘‘Dust
Bowl’’ of the 1930s. We believe that this
represents a unique history because
long-term BBS data (Sauer 2010a)
suggest a relatively stable population in
Colorado despite the dramatic drop in
numbers on the PNG. In 2008, Knopf
expressed the opinion that similar
numbers of mountain plover were
breeding in Weld County as in 1990,
just not on the PNG (Knopf 2008, p. 54).
We have no scientific information that
would point to the precipitous decline
in mountain plover historically at the
PNG as indicative of the overall
mountain plover population trend.
(32) Comment: One commenter
suggested that mountain plover
numbers are dynamic, and that their
current abundance is within the range of
normal fluctuation due to annual
variation in weather patterns.
Our Response: Breeding numbers and
nest success can vary locally based on
a number of factors including weather.
However, the historical reduction in
rangewide mountain plover numbers
seems well substantiated. Interpretation
of recent trends is made more difficult
by short-term variability in population
numbers that may reflect annual
weather variation. The effect of all
factors, natural and human-caused, that
may contribute to the survival of the
mountain plover is considered in this
determination, including variation in
weather patterns and longer-term
changes in climate.
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Species Vulnerability
(33) Comment: One commenter
referenced the mountain plover’s
relatively short lifespan as contributing
to the vulnerability of populations to
extirpation if one or more years of
unfavorable habitat on their breeding
grounds prevent successful nesting.
Our Response: As discussed above in
our discussion of Population Size and
Trends, and under Factor E below, our
former conclusion that the lifespan of
mountain plover contributed to its
vulnerability has been refuted based on
more recent information. The mountain
plover is now considered a relatively
long-lived species, with one individual
documented living for 10 years
(Dinsmore 2008, p. 52). We do not
believe that mountain plover lifespan
substantially influences the
vulnerability of mountain plover to
extinction.
(34) Comment: One commenter stated
that breeding mountain plover
populations are often discontinuous, in
part because of habitat fragmentation,
and stated that local, isolated mountain
plover populations have an increased
vulnerability to random natural and
human-caused events.
Our Response: It is generally true that
small and isolated populations are less
secure than larger populations. While
the mountain plover is a migratory,
highly mobile species, it generally
returns to the same breeding sites,
which isolates local populations to a
degree. Small mountain plover
populations are vulnerable to ‘‘blinking
out’’ if events destroy or degrade habitat.
This vulnerability may be offset by the
species’ ability to colonize new habitat
as it becomes available. Recent studies
describe mountain plover dispersal from
natal sites or former breeding sites, and
suggest that the mountain plover has
been able to disperse and exploit habitat
nearby if former habitat is destroyed.
Prairie Dog Issues
(35) Comment: We received numerous
comments regarding mountain plover
and prairie dogs. They included
comments regarding the mountain
plover’s dependence on prairie dogs,
and the distribution, abundance, and
trends in prairie dog populations. One
commenter contended that if the blacktailed prairie dog does not merit listing,
then the mountain plover does not
either.
Our Response: It is well established
that in parts of its range, Montana in
particular, the mountain plover is
largely dependent during breeding on
the habitat that prairie dogs create and
maintain. Elsewhere, mountain plover
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also breed in a variety of habitats,
including prairie, semi-desert, and
cropland. See our discussion regarding
the status and threats to the black-tailed
prairie dog and potential effect on the
mountain plover in Factor A below. We
recently determined that the blacktailed prairie dog does not warrant
listing under the Act (74 FR 63343,
December 3, 2009), but it does not
follow that this would automatically
lead to a similar conclusion for the
mountain plover since the species could
be subject to a variety of threats
unrelated to the status of prairie dogs.
(36) Comment: We received a
comment that the Service in 1999 and
2002 underestimated the presence of
prairie dogs and therefore their habitat
and the number of mountain plover that
prairie dog colonies supported.
Our Response: Our current analysis
includes information developed since
2002. Under Factor A below, we discuss
current estimates of prairie dog
abundance and implications of prairie
dog numbers to mountain plover.
(37) Comment: Some commenters
stated that black-tailed prairie dogs lack
protection, are often poisoned or shot,
and are often affected by sylvatic
plague; therefore, prairie dog colonies
and the mountain plover they support
remain vulnerable.
Our Response: We agree that there are
few protections for the black-tailed
prairie dog. However, despite the above
factors, the black-tailed prairie dog has
increased in number throughout all
States in its range in the United States
since the 1960s. In the United States, we
do not foresee any significant decreases
in black-tailed prairie dog populations
or the habitats they create. On December
3, 2009, the Service published a 12month finding that the black-tailed
prairie dog is not threatened with
extinction and is not likely to become so
in the foreseeable future (74 FR 63343).
In Mexico, both the black-tailed prairie
dog and the Mexican prairie dog
continue to be reduced in number and
distribution, and this likely impacts
mountain plover habitat. See our
discussion under Factor A below.
(38) Comment: Other commenters
cited conservation efforts that target
prairie dogs, as well as efforts to
conserve greater sage-grouse
(Centrocercus urophasianus), lesser
prairie-chicken (Tympanuchus
pallidicinctus), and black-footed ferret
(Mustela nigripes), and concluded that
these existing efforts make mountain
plover conservation efforts unnecessary.
Our Response: Efforts to conserve
these species are in response to declines
in numbers and threats to their future
existence. While the mountain plover
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will benefit from conservation of prairie
dogs, some other species require
habitats unlike those favored by the
mountain plover. To the extent that
mountain plover benefit from
conservation efforts for other species,
these are addressed under Factor A,
below.
(39) Comment: One commenter
contended that the presence of prairie
dogs was only one of several factors that
create mountain plover breeding habitat
and that soil type, soil moisture, cattle
grazing, fire, and incidence of drought
all play a role in supplying suitable
mountain plover breeding habitat.
Our Response: While the literature on
the mountain plover is replete with the
association of mountain plover and
prairie dog colonies, we agree that other
factors, singly or in combination, can
shape mountain plover breeding habitat,
and we have taken this into
consideration in this final listing
determination.
Grassland Conversion and Agricultural
Issues
(40) Comment: Multiple commenters
state that grassland conversion to
cropland is a significant threat.
Our Response: While grassland
conversion contributed to past
contraction in the mountain plover’s
range and reduction of the mountain
plover’s numbers, much of this took
place on the eastern Great Plains where
conversion to crops such as corn and
soybeans was feasible. The rate of
grassland conversion is now much
reduced. We do not believe that the
current or anticipated future conversion
of grasslands to other uses is a
significant threat. Dryland agriculture,
found in the southern portions of the
mountain plover’s breeding range,
supports significant numbers of
breeding mountain plover. The extent to
which the use of dryland agricultural
habitat is beneficial to the mountain
plover is largely undetermined. See our
discussion under Factor A below.
(41) Comment: One commenter
contended that current farming
practices benefit breeding mountain
plover, that mountain plover are an
adaptable species that have shifted from
grasslands to cultivated lands on both
their breeding and wintering areas, and
that cultivated lands are now the most
important habitat for the mountain
plover. Other commenters raised the
question of whether the choice to nest
in cropland is detrimental to mountain
plover.
Our Response: Research findings from
Colorado present a complex picture.
Hatching success on some croplands is
similar to that found on grasslands with
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or without prairie dogs. Chick survival
appears to be lower on crop fields, but
results of some studies differ, perhaps
depending on variables such as annual
weather conditions and site-specific
levels of predation. The influence of the
agricultural landscape on mountain
plover recruitment has not been fully
determined. Wintering mountain plover
favor crop fields at times, but habitat
preference seems to vary greatly by
region. Mountain plover use of crop
fields in winter may reflect the loss of
preferred native habitats.
(42) Comment: One commenter stated
that farming practices on the prairie
have not changed in 50 years and
questioned why they could suddenly be
a threat.
Our Response: Dryland farming
practices in eastern Colorado and
adjacent States have remained relatively
stable, although market factors may
favor one crop over another.
Historically, conversion of prairies to
crop fields likely contributed to the
decline of mountain plover, especially
in the eastern portion of its range. Farm
operations can directly impact nesting,
but the current relationship between
dryland crop fields and breeding
mountain plover is complex. However,
the best available information indicates
that current agricultural practices have
remained largely unchanged in recent
years and have not been shown to pose
a threat to the mountain plover (see
Factor A discussion below).
(43) Comment: Several commenters
stated that the Conservation Reserve
Program is beneficial to the mountain
plover, while other commenters thought
the program was detrimental to the
mountain plover.
Our Response: The U.S. Department
of Agriculture (USDA) administers the
Conservation Reserve Program, which
allows producers to retire agricultural
lands for a 10-year period, thereby
benefitting wildlife and other resources.
Most of these lands are planted with
nonnative grasses that support other
wildlife species but often do not create
mountain plover habitat. The program
likely has little effect on overall
mountain plover habitat because a
relatively small portion of agricultural
fields are retired at any one time and
retired lands provide minimal benefit to
mountain plover.
(44) Comment: Commenters expressed
concern that anticipated human
population growth in South Park, Park
County, Colorado, and the
fragmentation of existing habitat there,
will impact a significant mountain
plover population.
Our Response: We agree that buildout
of private lands in South Park would
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adversely affect the mountain plover
breeding population that is currently
present. However, based on information
from Park County, population growth is
much slower than once predicted, and
we do not anticipate substantial human
development will occur in the area in
the foreseeable future. See our
discussion under Factor A below.
Livestock/Grazing/Range Management
(45) Comment: One commenter stated
that range management has contributed
to the past decline of mountain plover
and is a current threat, as practices vary
little from those used previously.
Our Response: Range management is
often designed to maximize forage and
diminish excessive disturbance to grass
and soil. Such management, when
employed, does not benefit the
mountain plover. However, we do not
see range management as representing a
current or future threat to the mountain
plover, as there is no information to
suggest that current range management
practices and the habitat conditions
now present are likely to change
substantially in the future.
(46) Comment: One commenter cited
recommendations by Knopf and
Wunder (2006) to prioritize research
regarding varied livestock grazing
practices and their effects on mountain
plover.
Our Response: Research is ongoing as
to how range management affects
mountain plover and a variety of other
grassland species. We have a basic
understanding of how livestock grazing
can enhance mountain plover habitat
(Dechant et al. 2003, entire).
(47) Comment: Commenters cited the
decline in sheep (Ovis aries) numbers in
the mountain plover’s breeding range as
detrimental to mountain plover.
Our Response: Sheep grazing helps
maintain low vegetation structure
favored by the mountain plover. The
U.S. sheep industry has been in decline
since the 1940s. Past declines in sheep
may have contributed to losses in
mountain plover breeding habitat. The
future of the sheep industry in the
United States is difficult to predict. See
our discussion under Factor A below.
(48) Comment: One commenter stated
that cattle do not replace the role of
bison in the ecosystem, and that the role
of cattle grazing as it relates to insect
availability has not been adequately
evaluated.
Our Response: The historical loss of
bison resulted in a number of changes
to the prairie ecosystem. Current
mountain plover numbers and
distribution, and our evaluation of
threats to the species, are based on an
ecosystem largely devoid of bison.
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Insect numbers and availability to
mountain plover under various grazing
regimes may be worthy of investigation.
Mineral Extraction/Energy Development
(49) Comment: We received many
comments on the threat to the mountain
plover posed by oil and gas field
development, and wind energy
development. Commenters stated that
effects of energy development on the
mountain plover are largely unknown
and that the mountain plover’s response
to oil, gas, and wind energy
development should be investigated.
Our Response: We discuss the
potential impact of energy development
on mountain plover under Factor A
below. Wells, turbines, roadways, and
related development constitute potential
threats. While far from definitive, recent
studies suggest mountain plover may be
little affected by oil and gas
development. Thus far, we have no data
on the effect of wind energy
development on wintering mountain
plover.
(50) Comment: One commenter
recounted the history of mountain
plover presence at the Antelope Coal
Mine in Wyoming and suggested that
mountain plover are tolerant of both
ground disturbance and nearby
industrial activity.
Our Response: We agree that results of
monitoring at this site confirm the
mountain plover’s preference for open
ground created by disturbance and a
general tolerance of human activity.
While mining activity displaces
mountain plover, reclamation following
mining may restore habitat.
(51) Comment: One commenter
described new wind energy projects
under development in southern Texas
areas where mountain plover winter and
thought that the species would be
affected by the presence of turbines.
Our Response: As stated earlier, thus
far, we have no data on the effect of
wind energy development on wintering
mountain plover. The response of
mountain plover to turbines on their
breeding areas (which indicates some
degree of tolerance) may not provide
insight into how flocks respond in
winter.
(52) Comment: One commenter noted
conservation efforts to limit energy
development on State-designated greater
sage-grouse Core Breeding Areas in
Wyoming, which include 36 percent of
likely mountain plover breeding habitat
in the State. The commenter suggested
that this will provide a significant
measure of protection for the mountain
plover.
Our Response: While limitations on
energy development in these areas may
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reduce potential for any associated
adverse impacts on the mountain
plover, there is uncertainty as to
whether such measures will persist into
the future. Designated greater sagegrouse Core Breeding Areas are broad
and encompass habitats that support
mountain plover, but from a habitat
perspective, the needs of the two
species differ. Measures to manage for
the greater sage-grouse may not benefit
the mountain plover.
(53) Comment: One commenter
suggested that the Service should base
its analysis of the energy development
threats on what is known regarding the
impact of roads, habitat conversion, and
fragmentation. Others raised the issue of
roads and structures resulting in
increases in mammalian and avian
predators of mountain plover, which in
turn could lead to higher mortality of
mountain plover chicks and adults.
Our Response: In general, while some
other species have been shown to be
adversely impacted by energy
development, we have little evidence of
similar impacts on the mountain plover.
Changes in habitat brought on by energy
development, including the potential
that roads and structures may facilitate
increased predation on the mountain
plover, are addressed under Factor A
and Factor C below. Some adverse
impacts are likely, but there may also be
offsetting benefits resulting from the
increase in bare ground preferred by the
mountain plover.
(54) Comment: One commenter noted
that the Western Governors Association,
States, and the wind industry have been
addressing concerns regarding
construction of wind energy projects on
sensitive wildlife areas.
Our Response: The Service is engaged
with the wind industry and other
partners on issues regarding a range of
wildlife including the endangered
whooping crane (Grus americana), and
candidates including the greater sagegrouse, lesser prairie chicken, and
Sprague’s pipit (Anthus spragueii), as
well as the mountain plover. We
anticipate that current emphasis on
renewable energy projects will be
accompanied by cooperative initiatives
to minimize impacts to species of
concern.
(55) Comment: One commenter was
concerned that mountain plover
populations could decrease significantly
while studies on impacts from energy
development were ongoing and that
precautionary measures should be
enacted to preclude potential impacts.
Our Response: The USFS and BLM
have designated the mountain plover a
sensitive species within portions of the
range (see discussion under Factor D
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below). These agencies address
potential impacts to the species when
reviewing energy development.
However, we will continue to work with
these and other Federal agencies, States,
and other partners to monitor the status
of the mountain plover.
Wintering Habitat
(56) Comment: We received many
comments on actual or potential loss of
wintering habitat in California and how
this could affect rangewide populations
of mountain plover. Commenters stated
that the historical and ongoing
conversion of grasslands in California is
a threat to the mountain plover. Some
commenters cited Andres and Stone
(2009, p. 1), describing crucial threats
facing the mountain plover, including
‘‘* * * the inability to manage
agricultural lands in the Imperial
Valley, California, to provide consistent
winter habitat, and the loss or
inadequate management of other known
wintering areas in California.’’
Our Response: Much of the native
grassland that the mountain plover
formerly used for wintering in
California has been lost. While the
mountain plover has shown a
preference for native and nonnative
grasslands in California, especially
when heavily grazed, the mountain
plover has successfully switched to
using crop fields. Additional conversion
of grasslands to various other lands uses
may increase mountain plover
dependence on these crop fields. Any
resulting adverse effects of this change
are largely speculative.
Based on a variety of existing and
projected trends in land use, the further
reduction of grassland and crop fields
used by mountain plover for wintering
in California seems likely. However, as
of 2007, California supported over 25
million ac (10 million ha) of land in
farms, including 9.5 million ac (3.8
million ha) of cropland, 5.5 million
cattle, and 600,000 sheep (USDA 2010).
The mountain plover is a highly mobile
species that uses habitat
opportunistically in winter. The
mountain plover’s preference for certain
agricultural lands above others is well
documented. However, the pervasive
expanse of agriculture throughout the
Central Valley and Imperial Valley
suggests to us that, while current and
foreseeable future changes may reduce
favored wintering habitat, the quantity
and variety of agricultural habitat
remaining in California will continue to
provide sufficient wintering areas for
the mountain plover.
(57) Comment: One commenter noted
that in the Imperial Valley, an important
wintering area for mountain plover, the
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area of bermudagrass and alfalfa (crops
favored by the mountain plover) has
declined.
Our Response: Both bermudagrass
and alfalfa show recent declines in area
from 2005 to 2009 (Imperial Irrigation
District (IID) 2010). While area devoted
to all hay (including bermudagrass and
alfalfa) in the Imperial County varies
yearly, 233,000 ac (90,000 ha) were
present in both the 1997 and the 2007
(USDA Census of Agriculture (USDA)
2010). We do not have evidence
indicating the likelihood of long-term
future declines in acreage devoted to
these two crops.
(58) Comment: One commenter noted
that the wintering range of the mountain
plover in Texas is not well described
and that the species’ occurrence in
Texas is variable. There was concern
that habitat needs were not understood
and that Texas populations were not
receiving the attention they merited.
Our Response: We agree that
knowledge of mountain plover
wintering in Texas has been scant (as
described in Conservation Status and
Local Populations above). Distribution
is largely limited to private lands where
land use has varied little and where few
threats are known. New efforts to survey
abundance and habitat use of mountain
plover in Texas are currently under
way.
Pesticides
(59) Comment: Some commenters
expressed concern that use of pesticides
to control grasshoppers (family
Acrididae) and the Mormon cricket
(Anabrus simplex) reduces foods that
sustain breeding mountain plover,
especially chicks, in the mountain
plover’s breeding range.
Our Response: Efforts to control
grasshoppers and Mormon crickets are
generally limited to suppressing
populations in years and in areas where
infestations occur, and have the goal of
reducing densities to limit economic
impacts. While at times local mountain
plover populations could be affected by
these activities, we do not believe that
grasshopper and Mormon cricket
control represents a significant threat to
mountain plover populations. See our
further discussion under Factor E
below.
Climate
(60) Comment: Some commenters
suggested that climate change could
bring warmer and drier conditions that
may benefit mountain plover breeding.
Our Response: Mountain plover
breeding numbers and breeding success
can vary greatly based on a number of
factors, including annual weather
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variation. Anticipated changes in
climate will alter annual norms of
temperature and precipitation, but those
changes will likely vary across the
mountain plover’s breeding and
wintering range (see discussion under
Factor E below). Overall, we believe it
is speculative to conclude that these
effects will be beneficial to the
mountain plover.
contribute to continued cooperation
efforts with private landowners. Were
we to determine that the mountain
plover met the definition of a threatened
species, we would consider developing
a special rule under section 4(d) of the
Act. However, because we determined
that the species does not warrant listing,
the consideration of a special 4(d) rule
is not necessary.
Conservation Efforts and Effects of
Listing
(61) Comment: Several commenters
noted that conservation partnerships
between State agencies, landowners,
and conservation groups have promoted
conservation of mountain plover and
that listing would negate some gains in
cooperation.
Our Response: We agree that
partnerships are important to the
conservation of the mountain plover,
especially in those States where
mountain plover occur mostly on
private lands. The concern that such
partnerships could be affected by listing
is legitimate, but is not a factor
evaluated when determining whether a
species warrants listing under the Act.
(62) Comment: One commenter
suggested that traditional land uses on
private land would continue even if
listing occurred. Another commenter
suggested listing under the Act would
decrease the ability to effectively
manage habitat, slowing management
response to changing science and
conditions on the ground. A third
commenter suggested listing would
provide impetus for needed research.
Our Response: We agree that listing
under the Act could lead to multiple
outcomes, including those above. We
considered all available scientific and
commercial information in making our
determination as to whether the
mountain plover is currently, or may in
the foreseeable future become, in danger
of extinction.
(63) Comment: Several commenters
emphasized the importance of
developing a special rule under section
4(d) of the Act to exempt certain
activities from the take provisions of the
Act should the mountain plover be
listed.
Our Response: In our June 29, 2010,
document (75 FR 37353) we addressed
the possible development of a special
4(d) rule if the mountain plover were
listed as threatened. The intent was to
develop a mechanism by which
agricultural practices that might result
in take, but were believed to have no net
adverse impact on the mountain plover,
could continue. Development of such a
rule would allay some concerns
associated with listing and would
Summary of Information Pertaining to
Five Factors
Section 4 of the Act (16 U.S.C. 1533)
and implementing regulations (50 CFR
424) set forth procedures for adding
species to the Federal Lists of
Endangered and Threatened Wildlife
and Plants. Under section 4(a)(1) of the
Act, a species may be determined to be
endangered or threatened based on any
of the following five factors:
(A) The present or threatened
destruction, modification, or
curtailment of its habitat or range;
(B) Overutilization for commercial,
recreational, scientific, or educational
purposes;
(C) Disease or predation;
(D) The inadequacy of existing
regulatory mechanisms; or
(E) Other natural or manmade factors
affecting its continued existence.
The February 16, 1999 (64 FR 7587),
proposed listing rule provided a
description of threats affecting the
mountain plover under the five listing
factors identified in section 4(a)(1) of
the Act. The December 5, 2002, proposal
(67 FR 72396), which was described as
a ‘‘supplemental proposal,’’ provided
pertinent new information. Both of the
proposed rules concluded that the
mountain plover was likely to become
an endangered species in the foreseeable
future unless measures were taken to
reverse its decline. Conservation
measures to reverse the decline were
discussed in both of the proposals.
In our February 16, 1999, proposed
rule to list the species (64 FR 7587) and
our December 5, 2002, proposed rule to
list the species (67 FR 72396) we
described a number of potential threats
to the mountain plover. We cited
historical decline in the black-tailed
prairie dog (98 percent range wide) and
its effect on mountain plover habitat.
We described effects of past rangeland
loss to agricultural conversion (30
percent of the Great Plains) and more
recent conversion at specific mountain
plover breeding sites. We addressed
residential expansion into a mountain
plover breeding area in South Park,
Colorado, and stated that buildout of
private lands would be detrimental. We
hypothesized that cultivated areas used
for breeding by mountain plover may
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act as a ‘‘population sink’’ and that this
could impact population viability. We
expressed concern over the rising trend
in oil, gas, and mineral exploration in
mountain plover breeding habitat and,
while we suggested habitat changes
might not be detrimental, we cautioned
that roads and human disturbance could
impact mountain plover breeding. We
cited potential impacts of both historical
loss of grasslands and changing
agricultural practices on mountain
plover wintering areas in California.
With the Imperial Valley growing in
importance to wintering mountain
plover, we suggested that water
conservation, water transfer projects,
burning restrictions, urbanization, and
resulting modification of agricultural
practices in the Imperial Valley could be
detrimental to mountain plover
populations. In our 1999 and 2002
proposals we also expressed concerns
regarding the mountain plover’s average
life span and breeding site fidelity as
factors potentially impacting persistence
of local breeding populations. We
described a short average life span as
limiting opportunities for mountain
plover to reproduce. We also suggested
that high site fidelity and the specific
breeding habitat that mountain plover
required limited opportunities to
disperse to new breeding sites should
former breeding areas turn inhospitable.
We addressed concerns over mountain
plover exposure to pesticides; however,
we documented no deleterious effects.
In the nine years since our 2002
proposal, substantial new information
has been developed regarding the
mountain plover and potential threats to
its existence. Our December 3, 2009,
12-month finding on a petition to list
the black-tailed prairie dog summarized
new information on the species and
provided a basis for us to assess whether
threats to black-tailed prairie dog may,
in turn, affect the mountain plover (74
FR 63343). We now believe that the
black-tailed prairie dog is a resilient
species and that, overall, populations in
the mountain plover breeding range are
not likely to decline. Recent data
confirms that rangeland conversion to
agriculture remains insignificant across
the mountain plover’s breeding range.
Of the States where we previously
documented rangeland declines, none
have experienced significant decline in
rangeland in recent years. Expanded
human development of mountain plover
breeding habitat in South Park,
Colorado, did not proceed as previously
anticipated, and is not expected to do so
in the foreseeable future. Mountain
plover use of cultivated lands has been
further investigated, providing insight
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into the value of crop lands to breeding
mountain plover. It now appears that
perhaps one quarter of the rangewide
mountain plover population breeds in
crop fields and little evidence has
surfaced to suggest that is problematic.
Energy production in mountain plover
habitat continues to expand, including
increased development of oil and gas,
and wind energy projects. Studies to
date have not documented adverse
impacts of oil and gas development, or
wind energy projects. Effects of such
projects on mountain plover merit
continued study, largely because of their
potential future scope. In California,
land use changes continue in the
Imperial Valley and elsewhere.
However, based on current rangewide
mountain plover population estimates
(over 20,000 breeding birds) we now
believe that the majority of mountain
plover winter in areas other than
California. We conclude that even with
reduction of California wintering
habitat, sufficient area of wintering
habitat will remain, in California and
elsewhere, to support current
populations. Life span, site fidelity, and
dispersal of both adult and juvenile
mountain plovers have been further
investigated. Contrary to our previous
belief, the mountain plover is now
considered a relatively long-lived
species. Results of genetic research
provide evidence that mixing among
mountain plover breeding populations
is occurring. Dispersal, especially by
returning one year old mountain plover,
appears significant. Site fidelity and the
mountain plover’s ability to seek out
alternative sites for breeding are no
longer of concern. While substantially
more information has been developed
regarding exposure of mountain plover
to pesticides, no evidence of actual
impacts to individuals, or suggestions
that pesticides are having local or
rangewide impacts to the species have
surfaced.
The following summary builds on
scientific and commercial information
presented in our 1999 and 2002
proposals and provides our current
analysis based on all information
currently available.
Factor A. The Present or Threatened
Destruction, Modification, or
Curtailment of Habitat or Range
Recent summaries of the mountain
plover’s status (Dinsmore 2003; Knopf
and Wunder 2006; Andres and Stone
2009) have highlighted the loss or
degradation of mountain plover habitat
as the greatest threat to the species. The
primary issues that have been raised are
potential loss of prairie dog populations
and the mountain plover habitat they
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create; loss of native prairie and
rangeland habitats; cropland breeding
habitat as a potential reproductive sink;
oil, gas, and mineral development; wind
and solar energy development; loss and
changes to wintering habitat in
California; livestock grazing practices;
and urbanization. We address these
below.
Threats to Prairie Dogs and Associated
Loss of Habitat
Much of the mountain plover
breeding range described above follows
the range of the black-tailed prairie dog
on grasslands of the Great Plains from
Canada to Mexico. To a lesser extent,
mountain plover also breed within the
ranges of the white-tailed, Gunnison’s,
and Mexican prairie dogs. Mountain
plover often nest in black-tailed prairie
dog colonies at densities greater than in
other habitats (Childers and Dinsmore
2008, p. 707; Tipton et al. 2009, p. 496),
and mountain plover numbers have
been shown to track changes in prairie
dog abundance brought on by sylvatic
plague (Dinsmore et al. 2005, pp. 1550–
1551; Augustine et al. 2008,
unpaginated; Dinsmore and Smith 2010,
pp. 42–44). A common recommendation
regarding conservation of the mountain
plover is to assure the maintenance or
expansion of black-tailed prairie dog
populations and the landscapes they
create (Dinsmore et al. 2005, p. 1552;
Augustine et al. 2008; Knopf 2008, p.
61; Andres and Stone 2009, p. 35;
Dinsmore et al. 2010). Current and
future threats to the distribution and
abundance of prairie dogs, especially
the black-tailed prairie dog, may in turn
be threats to the mountain plover.
On December 3, 2009, the Service
published a 12-month finding on a
petition to list the black-tailed prairie
dog as endangered or threatened under
the Act (74 FR 63343). We found listing
to be not warranted. Here, we rely
heavily on the analysis and results of
that finding to assess the potential threat
to the mountain plover from current or
future loss of breeding habitat in the
United States that is created and
maintained by the black-tailed prairie
dog.
In our December 5, 2002, proposal to
list the mountain plover we discussed
historical reduction of the black-tailed
prairie dog numbers, but not current
populations or recent population trends
(67 FR 72402). In our 2009 finding
regarding the black-tailed prairie dog,
we estimated that 2.4 million ac (1
million ha) of occupied black-tailed
prairie dog habitat exists in a shifting
mosaic over time, throughout an
estimated 283 million ac (115 million
ha) of suitable habitat. We evaluated
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recent trends in occupied habitat and
considered occupied habitat an
appropriate surrogate for the status of
the species. Rangewide, we estimated
historical occupied area of black-tailed
prairie dog colonies to be between 80
million ac and 104 million ac (32 to 42
million ha), almost all in the United
States. Occupied area in the United
States had decreased to a low of 364,000
ac (147,000 ha) by 1961 (largely because
of eradication efforts), and subsequently
increased to the 2.4 million ac (1
million ha) cited above. Throughout the
United States, this represents a 600
percent increase in estimated blacktailed prairie dog numbers from 1961.
See our December 3, 2009, finding (74
FR 63343) for the methods used to
arrive at these estimates and cautions
regarding their accuracy.
The following evaluation of blacktailed prairie dog status highlights the
three States, Colorado, Montana, and
Wyoming, which have the greatest
number of breeding mountain plover
associated with black-tailed prairie dog
colonies. In Colorado, occupied blacktailed prairie dog habitat historically
existed in the eastern half of the State,
east of the Front Range Mountains (Hall
and Kelson 1959, p. 365). Currently, the
distribution of the black-tailed prairie
dog is scattered in remnant populations
throughout at least 75 percent of the
historical range (Van Pelt 2009, p. 14).
The most recent estimate of occupied
habitat is 788,657 ac (319,158 ha) (Odell
et al. 2008, p. 1311). This is
approximately one-third of all currently
occupied black-tailed prairie dog habitat
in the United States, and is an eight-fold
increase over occupied habitat thought
to be present in Colorado in 1961.
The Conservation Plan for Grassland
Species in Colorado (Conservation Plan)
(Colorado Division of Wildlife 2003, p.
1) has a goal ‘‘to ensure, at a minimum,
the viability of the black-tailed prairie
dog and associated species (mountain
plover, burrowing owl, swift fox, and
ferruginous hawk (Buteo regalis)) and
provide mechanisms to manage for
populations beyond minimum levels,
where possible, while addressing the
interests and rights of private
landowners.’’ The Conservation Plan
includes a species account for mountain
plover, but does not provide any
regulatory protections for the species or
its habitat.
In Montana, where mountain plover
are strongly associated with prairie dog
colonies (Childers and Dinsmore 2008,
p. 701), black-tailed prairie dog
occupied habitat historically existed in
the eastern two-thirds of the State, with
the exception of the northeastern corner
of the State (Hall and Kelson 1959, p.
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365). Current prairie dog distribution is
scattered in remnant populations over
90 percent of the historical range (Van
Pelt 2009, p. 20). Currently, 193,862 ac
(78,453 ha) of occupied habitat are
estimated to occur in Montana
(Hanauska-Brown 2009). This represents
nearly a seven-fold increase over
occupied habitat thought to be present
in Montana in 1961.
In Wyoming, the black-tailed prairie
dog historically occupied habitat in the
eastern half of the State, east of the
Rocky Mountains (Hall and Kelson
1959, p. 365). Currently, distribution is
scattered in remnant populations
throughout at least 75 percent of the
historical range (Van Pelt 2009, p. 40).
A 2006 study estimated the amount of
occupied habitat to be 229,607 ac
(92,919 ha) (Grenier et al. 2007, p. 125)
and these results suggested that blacktailed prairie dog populations in
Wyoming remain stable (Emmerich
2010, pers. comm.). This represents
nearly a five-fold increase over occupied
habitat thought to be present in
Wyoming since in 1961.
In the past, the conversion of native
prairie habitat or rangeland to cropland
reduced black-tailed prairie dog
colonies, and thereby impacted the
mountain plover’s most productive
breeding habitat in the grassland
ecosystem. Conversion of native prairie
to cropland historically progressed
across the Great Plains from east to
west. The most intensive farming
activity remains in the east, in portions
of North Dakota, South Dakota,
Nebraska, Kansas, Oklahoma, and
Texas, where higher rainfall amounts
and generally better soils result in
greater agricultural production, and the
land supports crops such as corn and
soybeans. This land conversion resulted
in the historical reduction in blacktailed prairie dog populations; as well as
reductions in mountain plover
populations in Nebraska, Kansas,
Oklahoma, and Texas; it also resulted in
the extirpation of the mountain plover
populations in North Dakota and South
Dakota. Land with the highest potential
for traditional farming uses was
converted many years ago. The threat of
future destruction of both prairie dog
and mountain plover habitat through
cropland conversion is minimal, much
less than in the early days of
agricultural development in the Great
Plains (see Loss of Breeding Habitat to
Land Conversion and Development,
below).
The present or threatened alteration of
habitat due to oil, gas, coalbed methane,
and mineral extraction, and wind
energy development, affects portions of
black-tailed prairie dog occupied
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habitat; however, we have no
information regarding the extent of
potential impacts. Nevertheless, prairie
dog occupancy has apparently increased
within oil and gas development areas in
Wyoming (Sorensen et al. 2009, pp. 5–
6). We have no evidence that present or
threatened curtailment of habitat due to
oil, gas, coalbed methane, and mineral
extraction, and wind energy
development, is a limiting factor for the
black-tailed prairie dog in Wyoming or
elsewhere throughout its range.
Approximately 110 million ac (45
million ha) of cropland and 283 million
ac (115 million ha) of rangeland occur
within the black-tailed prairie dog’s
range at present (Ernst 2008, pp. 10–19).
In our December 3, 2009, finding for the
black-tailed prairie dog (74 FR 63343),
we contrasted the 2.4 million ac (1
million ha) of currently occupied
habitat with the 283 million ac (115
million ha) of rangeland and concluded
that sufficient potential habitat still
occurs within the range of the species in
the United States to accommodate large
expansions of prairie dog populations
(which in turn would benefit the
mountain plover) if the landowners and
public sentiment allow. We concluded
that the present or threatened
destruction, modification, or
curtailment of habitat or range is not a
limiting factor for the black-tailed
prairie dog and that we do not
anticipate that impacts from habitat loss
are likely to negatively impact the status
of the species in the foreseeable future.
Because of the association between the
mountain plover and the black-tailed
prairie dog, we believe that appropriate
habitat to support prairie dog colonies is
not a limiting factor within the breeding
range of the mountain plover.
Sylvatic plague is an exotic disease
foreign to the evolutionary history of
North American prairie dogs. It is
caused by the bacterium Yersinia pestis.
Black-tailed prairie dogs are very
sensitive to sylvatic plague, and
mortality in colonies affected frequently
reaches 100 percent. Sylvatic plague has
expanded its range to all States within
the range of the black-tailed prairie dog
in recent years and has caused local
population declines at several sites.
These declines are typically followed by
partial or complete recovery. Rangewide
and Statewide estimates of prairie dog
occupied area did not include
unoccupied prairie dog colonies where
sylvatic plague (or poisoning) had at
least temporarily eliminated prairie
dogs. Over all prairie dog colonies,
unoccupied area was found to total
12 percent in Colorado, 15 percent in
Montana, and 13 percent in Wyoming.
The BLM mapped prairie dog colonies
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in Phillips County, Montana in 2004
and 2005, and returned to 50 randomly
selected prairie dog colonies in 2010. Of
the 50 colonies selected for sampling, 48
were still active in 2010 (McDonald
2010). In the changing mosaic, colonies
lost or temporarily inactive may be
offset by colonies reoccupied or newly
established.
We documented in our 12-month
finding on a petition to list the blacktailed prairie dog that, since the early
1960s, occupied black-tailed prairie dog
habitat has increased in every State,
even in those States where sylvatic
plague has been present for over 50
years (74 FR 63355–63356). This
increase has occurred despite continued
impacts from sylvatic plague and other
threats. In our 2009 finding, we
concluded that the status of the blacktailed prairie dog, as indicated by
increased occupied habitat since the
early 1960s, indicates that sylvatic
plague is not a limiting factor for the
species (74 FR 63357).
Similarly, the increase in black-tailed
prairie dog numbers in the United States
has occurred despite conflicting Federal
and State regulations and policies that
encourage conservation of prairie dogs
through development of State and
rangewide management plans, yet in
many cases continue to allow shooting
and poisoning of prairie dogs.
Nevertheless, affected Federal and State
agencies are engaged in black-tailed
prairie dog management and monitoring
to a much greater extent than they were
10 years ago.
Efforts to conserve the black-tailed
prairie dog will likely be beneficial to
the mountain plover. Our December 3,
2009, finding for the black-tailed prairie
dog (74 FR 63343) described the 1998
establishment of the Black-tailed Prairie
Dog Conservation Team, with
representatives from each State within
the historical range of the species, and
the development of ‘‘The Black-tailed
Prairie Dog Conservation Assessment
and Strategy’’ (Van Pelt 1999, entire),
which initiated development of ‘‘A
Multi-State Conservation Plan for the
Black-tailed Prairie Dog, Cynomys
ludovicianus, in the United States’’
(Multi-State Plan) (Luce 2002). The
purpose of the Multi-State Plan was to
provide adaptive management goals for
future prairie dog management in the 11
States within the species’ range. The
plan identified 10-year target objectives
including maintaining and increasing
occupied acreage of black-tailed prairie
dog habitat, and increasing the number
of large prairie dog complexes. The
States also agreed to draft Statewide
management plans for the black-tailed
prairie dog. The States approve their
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own Statewide management plans.
Colorado and Wyoming have finalized
grassland conservation plans that
support and meet the objectives of the
Multi-State Plan. However, Montana is
among the States that have finalized
management plans that do not support
or meet all of the objectives of the MultiState Plan. These and other efforts give
promise that the trend of increasing
black-tailed prairie dogs populations
since 1961 can be sustained.
Climate change will likely affect
black-tailed prairie dogs and their
habitat; however, at this time we have
no information on the direct
relationship between climate change
and black-tailed prairie dog population
trends, and we cannot quantify the
potential magnitude or extent of impact
that climate change may have on the
species. While climate change may
potentially impact the species in future
decades, particularly through its effects
on sylvatic plague, it is not apparent
that a net loss in occupied habitat will
result. The current status of the blacktailed prairie dog does not suggest that
the combined effects of sylvatic plague
and climate change are currently
limiting factors for the species or that
they will become so within the
foreseeable future, and we do not
believe climate change will result in
significant population-level impacts to
the black-tailed prairie dog.
In summary, we believe that the
black-tailed prairie dog is a resilient
species and that overall United States
populations are not expected to be
significantly affected by habitat loss due
to conversion to cropland, sylvatic
plague, shooting, poisoning, or climate
change (74 FR 63364, December 3,
2009).
Mountain plover populations in
Montana, and to a lesser extent other
breeding areas, are dependent on the
prairie dog for breeding habitat. Given
our conclusion that habitat created or
enhanced by black-tailed prairie dogs is
unlikely to decrease, we conclude that
threats to the black-tailed prairie dog in
the United States do not represent a
threat to the continued existence of the
mountain plover.
Potential dependence of both
wintering and breeding mountain plover
populations on remaining prairie dog
colonies in Mexico is of concern
(Macias-Duarte and Panjabi 2010, pp.
9–10). In Mexico, decline of native
grasslands supporting the black-tailed
prairie dog and the Federally
endangered Mexican prairie dog have
been extensive, despite some
environmental regulations designed to
protect prairie dogs and their habitats.
The large black-tailed prairie dog
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complex at Janos has been reduced by
73 percent since 1988, to approximately
38,000 ac (16,000 ha), while Mexican
prairie dog colonies within the El Tokio
region have also been reduced to
approximately 79,000 ac (32,000 ha)
(Andres and Stone 2009, p. 28; Ceballos
et al. 2010, pp, 7–8; Macias-Duarte and
Punjabi 2010, p. 9–10). Both areas, at
least in some years, support significant
numbers of wintering mountain plover
(see Conservation Status and Local
Populations above). Destruction and
fragmentation of prairie dog colonies
has occurred through poisoning and
shooting of prairie dogs, conversion to
cattle ranching or farming, overgrazing,
and drought. Mexico experienced a
prolonged drought in the Janos area in
recent years, which resulted in dramatic
loss of vegetation, followed by a
reduction in black-tailed prairie dog
occupied habitat (Larson 2008, p. 87).
These losses in prairie dog habitat in
Mexico have degraded or eliminated the
extent of wintering plover habitat in
these areas. Recent efforts to protect
prairie dogs and grasslands also benefit
wintering mountain plover and may
help stop or reverse recent trends.
Government designation of protected
areas in Chihuahua and Nuevo Leon,
and efforts by Pronatura Noreste, The
Nature Conservancy, and other
institutions, hold promise (Andres and
Stone 2009, pp. 33, 40; Macias-Duarte
and Punjabi 2010, p. 10). In 2009, the
1.3-million-ac (526,000-ha) Janos
Biosphere Reserve was established to
protect some of the best remaining
shortgrass prairie in Mexico and thereby
benefit the black-tailed prairie dog. This
conservation initiative is led by
Mexico’s National Protected Areas
Commission and the Chihuahuan State
government (The Nature Conservancy
2010). The Llano de la Soledad, which
encompasses the major Mexican prairie
dog complexes of the El Tokio area, a
26,000-ac (10,500-ha) area, has been
designated a State Natural Area for
Ecological Conservation administered
by the Agency of Environmental
Protection and Natural Resources of
Nuevo Leon. Neotropical migratory bird
grants from the Service have supported
efforts led by Pronatura Noreste to
protect and manage key lands through
purchase and easement. While past
habitat loss for the mountain plover at
Janos and El Tokio has been significant,
international attention to these and to
other important grassland complexes in
Mexico improves prospects for future
conservation and maintenance of
mountain plover wintering habitat.
Knowledge of mountain plover
breeding on prairie dog colonies in
Mexico is limited. The primary known
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value of black-tailed and Mexican
prairie dog colonies to the mountain
plover is as wintering habitat; yet use
varies greatly from year to year.
Mountain plover use of croplands and
rangelands present in Mexico for
wintering is largely unstudied. For
example, agricultural areas in northern
Baja California, the coastal plains of
Sonora and Sinaloa, and throughout the
northern Chihuahuan Desert States may
potentially support substantial
wintering populations (Macias-Duarte
and Punjabi 2010, p. 10). The net effect
of reduction in prairie dog colonies in
Mexico to mountain plover is largely
unknown. However, given that
mountain plover winter extensively in
cropland habitats in California and
Texas, we believe that cropland habitats
in Mexico are likely available as
alternative wintering habitat. There is
no available information to indicate that
the past, current, or potential future loss
of black-tailed and Mexican prairie dog
colonies and the ecosystems they
support in Mexico is a significant threat
to the mountain plover.
Despite the ongoing effects of habitat
conversion, sylvatic plague, shooting
and poisoning, and lack of regulatory
mechanisms that provide protection,
black-tailed prairie dog habitats have
increased in the United States over the
last 50 years (74 FR 63343, December 3,
2009). Although there is significant
concern about the status of black-tailed
and Mexican prairie dogs and their
habitats in Mexico, there is no
information available to indicate that
further reductions in prairie dogs in
Mexico are threatening the mountain
plover. At this time, the best available
scientific information does not indicate
that the loss of prairie dog habitat is
likely to threaten the mountain plover
now or in the foreseeable future.
Loss of Breeding Habitat to Land
Conversion and Development
As described above, losses of native
grasslands in the Great Plains have been
severe since European settlement.
Losses of these native grasslands have
been greatest in the eastern Great Plains
and have impacted the mountain plover
mainly from conversion of prairie
grasslands to crop fields incompatible
with mountain plover breeding,
including those planted to corn and
soybeans. These losses are likely the
reason why the mountain plover no
longer breeds in the Dakotas, has a
limited range in Nebraska, and is now
a rare breeder in Kansas (Graul and
Webster 1976, p. 266; Knopf and
Wunder 2006). Land conversion to
agriculture continues, primarily in the
northern Great Plains, but at a much
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slower rate. Over the 15-year period
from 1982 to 1997, in Montana,
Wyoming, and Colorado, there were no
decreases in the amount of rangeland or
pastureland present (USDA 2010).
Conversion to cropland may be locally
affecting mountain plover in some areas
of Montana. Approximately 47,000 ac
(19,000 ha) of native grassland was
converted to agriculture in Montana
from 2005 to 2009 (Ducks Unlimited,
cited in McDonald 2010). Statewide, the
amount of cropland in Montana
increased by about 3 percent from 1997
to 2007 (USDA 2010). In the four
Montana counties with the most
mountain plover habitat (Blain, Fergus,
Phillips, and Valley Counties), cropland
increased over the same period by about
6 percent, with most of the increase
attributable to Valley County (USDA
2010). However, the cited conversion
from 2005 to 2009 represents less than
0.2 percent of the 30 million ac (12
million ha) of ‘‘grassland/herbaceous’’
cover present in Montana in 2001
(USGS 2001). Cropland is used by
breeding mountain plover elsewhere,
but its potential for use in Montana is
unknown. Conversion of grasslands to
cropland in Montana may locally
impact mountain plover; however, we
believe this low rate of conversion
would have negligible rangewide effect.
The best information available does
not allow us to estimate the specific
amount of occupied grassland breeding
habitat for mountain plover that has
been converted to other uses in recent
years. However, given the apparent low
rate of grassland conversion in Montana
and rangewide, and the mountain
plover’s ability to use grassland that has
been converted to other uses such as
certain agricultural crops including
wheat, sorghum, and millet, we believe
that grassland conversion does not pose
a substantial threat to the mountain
plover in Montana, or elsewhere in its
breeding range, now or in the
foreseeable future.
In our 1999 and 2002 proposals to list
the mountain plover as a threatened
species (64 FR 7587 and 67 FR 72396,
respectively), we also addressed the
concern that grassland breeding habitat
may be lost to human development.
Since the mountain plover’s breeding
range is extensive, there are
undoubtedly instances where human
development is and will locally displace
the mountain plover. We agree with the
conclusion of Andres and Stone (2009,
p. 22) that habitat in the mountain
plover breeding range is subject to little
overall threat from residential and
commercial development, because
human development is not expected to
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be very extensive in the largely rural
areas of the species’ breeding habitat.
An area that generated past concern in
our 1999 and 2002 proposals is South
Park, Park County, Colorado, an
approximately 480,000 ac (200,000 ha)
grassland basin where the mountain
plover breeding population is estimated
to be about 2,300 birds. Much of the
mountain plover habitat in South Park
is privately owned, and 32 percent of
this area has been subdivided (Granau
and Wunder 2001, pp. 8–9). Substantial
build-out of those properties currently
subdivided would be detrimental to
mountain plover; however, human
population growth in South Park is
modest (Nichols 2010, pers. comm.).
Many of the subdivisions occurred in
the 1960s and 1970s, and have not been
developed. Earlier forecasts suggested
South Park would have a human
population of 10,000 by 2010, but the
current human population stands at
approximately 3,500 (Nichols 2010,
pers. comm.). Issuance of building
permits countywide have decreased
steadily in recent years, from 297 in
2002 to 70 in 2009 (Carrington 2010,
pers. comm.). In addition, land
protection and conservation efforts by
the BLM, Park County, Colorado Open
Lands, and The Nature Conservancy are
ongoing in South Park. The BLM (2009a,
p. 2) amended their Royal Gorge
Resource Area Management Plan for the
South Park Subregion in light of new
resource goals, including the protection
of mountain plover breeding habitat.
Their Land Tenure Designation Plan for
South Park was modified to keep a
greater portion of the BLM’s
approximately 63,000 ac (26,000 ha) of
South Park lands in Federal ownership
and make less sensitive BLM lands
available for exchange to consolidate
Federal lands of highest resource value.
Primary goals of Park County’s Master
Plan include protection of
environmentally sensitive areas, and
managing the location and pace of
residential growth (Park County 2001, p.
13). In addition, Colorado Open Lands
and their partners have preserved
approximately 17,000 ac (7,000 ha) of
lands in South Park to minimize
development in and around significant
conservation areas (Colorado Open
Lands 2011).
The current level of residential
development in South Park is not
currently a threat to the mountain
plover and, given recent development
trends and conservation initiatives, we
do not consider residential development
in South Park to be a threat in the
foreseeable future. Elsewhere, threats
from human development are largely
limited to wintering habitat.
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In summary, we do not believe that
conversion of the mountain plover’s
grassland breeding habitat to cropland,
or to human residential and commercial
development, represents a threat to the
mountain plover now or in the
foreseeable future.
Range Management
Breeding mountain plover in
grasslands are strongly associated with
heavy grazing and soil disturbance
(Knopf and Wunder 2006). In the
absence of prairie dogs, activities such
as heavy cattle grazing, the
concentration of cattle at loafing areas
and at water, and burning of rangeland
provide habitat for mountain plover.
However, typical range management
practices such as fencing, rotational
grazing, decreased stocking rates, and
planting nonnative grasses to improve
soil moisture promote uniform
vegetative cover and taller grasses,
which are less beneficial to breeding
mountain plover. In addition, human
efforts to suppress wildfire are generally
detrimental to mountain plover.
Specific range management options
for mountain plover are somewhat
limited. Cattle grazing provides benefits
to mountain plover, but this is
especially true when it maintains low
vegetation and patches of bare ground.
Heavy cattle grazing may not be a
financially justifiable option for
ranchers and can create conditions
unfavorable to many other species of
wildlife. Aside from grazing, specific
range management options for mountain
plover are somewhat limited. Mountain
plover use burned areas for breeding,
and prescribed burning can be used as
a habitat management tool (Knopf 2008,
p. 61; Andres and Stone 2009, p. 29).
Ongoing USFS burning programs on the
PNG and the Comanche National
Grasslands in Colorado to attract
breeding mountain plover have had
some success (Augustine 2010a, pers.
comm.). However, primary benefits of
burning a site are generally of short
duration, i.e., 1 or 2 years (Augustine
2010b, pers. comm.). The value of
burning is dependent on the extent and
the frequency of burns. Augustine and
Malchunas (2009, p. 89) suggested that
late winter shortgrass burns may have
neutral or positive consequences for
livestock, but burning is not a
management practice generally
employed within the mountain plover’s
breeding range.
Even without rangeland management
that specifically benefits the mountain
plover, soil type, site history, or drought
may create habitat conditions that are
beneficial to breeding mountain plover.
Rocky or clay pan substrate may
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suppress vegetation and provide
breeding habitat (Knopf and Wunder
2006). In years of low precipitation,
grazing at relatively low intensity has a
greater impact on grassland vegetation
and can produce habitat conditions
favorable for mountain plover breeding.
Knopf (2008, entire) provided an
historical account of mountain plover
populations on the PNG, Weld County,
Colorado, and discussed the future of
mountain plover in the area. He
suggested that mountain plover
numbers in the area had been in decline
since the post-dust bowl days of the late
1930s and early 1940s, and that the
dramatic decline in the mid-1990s was
the abrupt end point of a process of
deteriorating mountain plover habitat
(recovery of grassland habitat), which
was exacerbated by other factors such as
wet spring weather and predation
(Knopf 2008, p. 60). Given current range
management practices, Knopf suggested
that short-term benefits from prescribed
burning and, more significantly, the
maintenance of prairie dog colonies
were the only viable means to enhance
mountain plover habitat on the PNG.
Sheep grazing can maintain the low
vegetation structure that is beneficial to
breeding mountain plover. However, the
current level of sheep grazing does not
maintain significant amounts of
mountain plover breeding habitat
rangewide. The sheep industry in the
United States has been in decline for
more than 60 years and now supports
about one-tenth of the number of sheep
present in the 1940s. Decreases in sheep
grazing may have been a contributing
factor to loss of favorable grassland
breeding habitat for the mountain plover
in the past. The future of the industry
is uncertain; continued declines in the
industry are likely in some areas, but
changes in the industry also present
opportunities for its growth (National
Academy of Sciences 2008, p. 4). For
the foreseeable future, it appears likely
that sheep grazing will remain a minor
rangewide contributor to maintenance
of favorable mountain plover breeding
habitat, but that potential for any further
decline in breeding habitat due to
additional loss of acreage grazed by
sheep is minimal.
A number of conservation efforts
target the conservation of grasslands,
prairie ecosystems, and prairie birds:
The Great Plains Landscape
Conservation Cooperative (a public/
private initiative to proactively conserve
declining habitats on private lands); The
Nature Conservancy’s ecoregional plan
for the Central Shortgrass Prairie; the
Colorado Division of Wildlife’s
Conservation Plan for Grassland Species
and similar efforts in other States;
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Natural Resources Conservation Service
conservation efforts under the Farm Bill;
preservation of grasslands via
conservation easements, including more
than 350,000 ac (140,000 ha) in
easements reported by the Colorado
Cattleman’s Agricultural Land Trust
(2010); the Rocky Mountain Bird
Observatory’s Prairie Partners; and The
Nature Conservancy’s ‘‘Prairie Wings’’
effort. Many of these initiatives include
conservation of the mountain plover,
the black-tailed prairie dog, and other
species supported by the prairie dog
ecosystem.
In summary, the extent to which
mountain plover are benefitted by cattle
grazing on any given site is determined
by the range management practices
employed. While some current
management practices result in habitat
conditions that are not optimal for
mountain plover breeding, a large
number of mountain plover nest on
rangeland. We do not anticipate future
changes to the current pattern of range
management across the breeding range
of the mountain plover that would
prove detrimental to the mountain
plover and its habitat. The extent to
which range management practices
could benefit the mountain plover in the
future is dependent on conservation of
black-tailed prairie dog colonies and, to
a lesser extent, on willingness to employ
prescribed burning as a range
management tool. Grazing by sheep can
create favorable breeding habitat for
mountain plover. The sheep industry in
the western United States has declined
over time, but we do not anticipate that
future changes in the sheep industry
will have a net negative impact on
existing mountain plover habitat or be a
threat to existing mountain plover
habitat in the future.
Cultivated Areas in the Mountain Plover
Breeding Range Acting as a Potential
Population Sink
Agricultural practices can destroy
mountain plover nests and eggs from
mechanical treatment (tilling, planting,
application of fertilizers and pesticides),
and crops growing beyond a certain
height may cause nest abandonment
(Knopf and Rupert 1999, p. 85;
Dinsmore 2003, p. 27). In our 1999 and
2002 proposals to list the mountain
plover as a threatened species (64 FR
7587 and 67 FR 72396, respectively), we
raised the concern that these activities
could create a reproductive ‘‘sink,’’ or in
other words a situation in which
mountain plover are drawn to crop
fields for nesting but do not produce
viable young at a rate that would sustain
the population.
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Knopf and Rupert (1999, p. 84)
suggested that breeding mountain
plover having the opportunity to nest on
either agricultural or prairie areas chose
both equally. In the eastern Colorado
shortgrass prairie ecosystem, mountain
plover breeding densities on crop fields
were twice as high as the densities
found on grasslands without prairie
dogs, although only one-fifth as high as
the densities found on prairie dog
colonies (Tipton et al. 2009, p. 496).
Based on the area of habitats surveyed
and densities of mountain plover
estimated, approximately 40 percent of
mountain plover may use crop fields for
nesting in eastern Colorado. Nebraska
studies (Van der Burg et al. 2010, pp. 48,
50) suggested a similar percentage of the
mountain plover in Nebraska utilize
crop fields for nesting. The small,
seemingly stable, breeding mountain
plover population in Oklahoma was
primarily found in plowed or fallow
fields, although again the potential of a
reproductive sink was raised
(MacConnell et al. 2009, pp. 31–33).
Based on estimates of mountain plover
using crop fields in Colorado and
Nebraska, together with known use of
crop fields in Wyoming, Oklahoma, and
Kansas, we conclude that up to one
quarter of all mountain plover may
utilize crop fields for breeding. Given
the significance of crop fields to
breeding mountain plover and questions
regarding a possible reproductive sink,
research is ongoing to better understand
the role that crop fields play in support
of breeding mountain plover
populations (Dreitz et al. 2010).
In Colorado, mountain plover
hatching success was found to be
similar in native grasslands and crop
fields, although causes of nest mortality
differed between the two habitats
(Dreitz and Knopf 2007, pp. 684–685).
Use of crop fields was not determined
to be detrimental to mountain plover
hatching success. However, a
subsequent eastern Colorado study
found chick survival to be similar on
crop fields (23 percent) to shortgrass
habitat without prairie dogs (24
percent), but lower than chick survival
on shortgrass habitat occupied by blacktailed prairie dogs (75 percent), and the
author again suggested that crop fields
may represent a reproductive sink or
‘‘ecological trap’’ (Dreitz 2009, pp. 875–
877). Given the study results, the same
concern could be raised regarding
shortgrass habitat lacking prairie dogs.
In contrast to the study above, recent
research on crop fields in Nebraska
found 95 percent survival of chicks of
adult mountain plover tracked for 35
days (Blakesley and Jorgensen 2010,
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pers. comm.), although loss of contact
with other adult mountain plover
suggests that actual chick survival was
somewhat lower (Blakesley 2010, pers.
comm.). Preliminary data from studies
of radio-tracked chicks in Montana and
Colorado in 2010 (Dreitz et al. 2010) did
not show chick survival in crop fields
to be lower than in other habitats. While
results reported by Dreitz (2009, pp.
875–877) above come from the most
comprehensive study of chick survival
in crop fields, other studies indicate that
mountain plover chick survival rates on
crop fields and among other prairie
habitats vary greatly in time and place.
Shackford et al. (1999, p. 119)
suggested that decreasing nest loss from
mechanical treatment of fields would
benefit mountain plover. Nest marking
efforts that allow farmers to avoid nests
and reduce nest mortality from
agricultural operations have been
conducted with cooperating farmers in
Colorado and Nebraska (Dreitz and
Knopf 2007, p. 685; Lock and
VerCauteren 2008, entire; Bly 2010a).
The Colorado Division of Wildlife and
the Nebraska Game and Parks
Commission, along with the Rocky
Mountain Bird Observatory, initiated
nest marking programs. In Nebraska, a
reported 80 percent of 246 nests marked
in crop fields over 3 years successfully
hatched young (Bly 2010a). As a
comparison, an experiment using
dummy nests suggested a 35 percent
success rate was likely in crop fields if
nests were not marked (Bly 2010a).
While recent analysis of mountain
plover populations suggests that efforts
targeting chick survival may hold more
conservation value than those efforts to
enhance nest success, management
techniques to achieve higher chick
survival may be difficult to employ. In
addition, nest marking programs have
helped establish ties between the
agricultural community and wildlife
managers (Dreitz and Knopf 2007, pp.
685–686; VerCauteren 2010). Outreach
efforts to farmers continue, including
education regarding mountain plover
and transition from nest marking to
landowners’ taking the lead in finding
and avoiding mountain plover nests in
the course of their field operations.
Community efforts, such as the annual
Mountain Plover Festival sponsored by
the Karval Community Alliance in
Lincoln County, Colorado, promote
stewardship of the mountain plover and
other wildlife as an integral part of both
farming and ranching practices.
Studies documenting numbers and
reproductive success of mountain
plover breeding on crop fields in eastern
Colorado and Nebraska do not entirely
resolve the issue of the relative value of
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this habitat to the mountain plover.
However, in studies from eastern
Colorado, nest success in crop fields
(Dreitz and Knopf 2007, pp. 684–685)
and chick survival in crop fields (Dreitz
2009, pp. 875–877; Dreitz et al. 2010)
appear similar to nest success and chick
survival in native shortgrass without
prairie dogs. We conclude that crop
fields support breeding mountain plover
as well as shortgrass without prairie
dogs, although likely not as well as
shortgrass with prairie dogs. If the crop
fields in eastern Colorado that are
regularly occupied by breeding
mountain plover are a reproductive
sink, their continued occupancy by
mountain plover is dependent on a net
influx of birds dispersing from other
breeding habitats. We have no evidence
to suggest whether or not this is
occurring. Further, unless mountain
plover prefer and choose crop fields for
breeding over available (unoccupied)
habitat where reproductive success is
higher, breeding in crop fields, even if
less successful, would not seem
detrimental. We conclude that, based on
the information available, the mountain
plover’s use of crop fields for breeding
does not represent a threat to the
species.
Another concern is the potential that
change in current agricultural practices
will result in future loss of the types of
crop fields that currently provide
breeding habitat for mountain plover.
Dryland agriculture is the type of
agriculture that most frequently
supports breeding mountain plover, and
it is dominated by wheat, but also
includes crops of sorghum, millet, and
sunflowers. Annual variation in the use
of dryland agriculture fields is dictated
by a number of factors including
weather, government programs, crop
prices, and preferences of individual
farmers. It is not known whether any
significant future changes to dryland
agriculture that the mountain plover
uses for breeding are likely to occur or
how they would affect mountain plover
(Andres and Stone 2009, p. 23).
In recent years, ethanol production
from corn has expanded in the United
States; however, most corn is cultivated
east of the range of the mountain plover
(Westcott 2007, pp. 1–3). Additionally,
the increase in corn production largely
occurs by adjusting crop rotations
between corn and soybeans (Westcott
2007, p. 7); neither crop regularly
supports mountain plover. We do not
anticipate that increased ethanol
production will result in a substantial
loss in the species’ occupied or
potential habitat because the majority of
this activity lies outside the range of the
mountain plover.
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In conclusion, we believe that
approximately one quarter of the
rangewide mountain plover population
breeds in crop fields in Colorado,
Nebraska, or elsewhere, but there is no
evidence that this represents a
reproductive sink detrimental to the
rangewide population. Dryland
agriculture has changed little over
recent decades, and we have little
evidence to suggest that crop fields now,
or in the future, represent a significant
threat to the mountain plover.
Energy and Mineral Development
Development targeting oil and gas,
coal bed methane, wind energy, and
other mineral resources is extensive
within the breeding range of the
mountain plover. Energy development
is a national priority as mandated by
Executive Orders 13212 (Actions to
Expedite Energy-Related Projects) (66
FR 28357, May 22, 2001) and 13514
(Federal Leadership in Environmental,
Energy, and Economic Performance) (74
FR 52117, October 8, 2009), and the
Energy Independence and Security Act
of 2007 (42 U.S.C. 17001 et seq.).
Current permitting and construction of
new energy projects on Federal and
non-Federal lands reflects this priority.
The development of energy resources
requires construction at well or wind
turbine sites, as well as access roads,
pipelines, power lines, and other
support facilities. These projects could
have an immediate effect on breeding
mountain plover due to disturbance and
habitat conversion, and secondary
effects associated with operation and
maintenance.
The magnitude of the issue is best
exemplified by energy development in
Wyoming, where the Wyoming Natural
Diversity Database (WYNDD) (2010) has
used habitat mapping and mountain
plover observation records to map the
probability of mountain plover
presence. In Wyoming, WYNDD (2010)
predicts a high probability of mountain
plover occurrence over about 7 million
ac (3 million ha) and a medium
probability of occurrence over about 14
million ac (6 million ha). We evaluated
overlap between predicted mountain
plover presence and energy
development (Lindstom 2010).
As of February 2010, 5,043 wells,
approximately 12 percent of operating
oil and gas wells in Wyoming (Wyoming
Oil and Gas Commission 2010),
occurred in areas of high probability of
mountain plover occurrence, while
13,266 wells, about 32 percent of wells,
occurred in areas with medium
probability of mountain plover
occurrence. While wells are clustered in
well fields, this would equate to one
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well per about 1,400 ac (560 ha) in areas
of high probability of mountain plover
occurrence and one well per 1,080 ac
(430 ha) in areas medium probability of
occurrence. We believe that this
represents a relatively low overall
potential impact to mountain plover
habitat.
Of 13 million ac (6 million ha) of
authorized (both developed and
undeveloped) BLM oil and gas leases in
Wyoming (BLM 2009b), we estimated
that 52 percent were in areas of high or
medium probability of mountain plover
occurrence (or about one-third of all
areas of high or medium probability of
mountain plover occurrence were under
BLM lease).
Areas in Wyoming of wind classes 4
through 7 (a measure of wind resource
potential) account for about 6 million ac
(2.4 million ha), or about 30 percent, of
those areas of high or medium
probability of mountain plover
occurrence (National Renewable Energy
Laboratory 2002). Since additional
factors determine development
potential, only a portion of these areas
would likely see future wind energy
development.
Future energy development will
depend on whether oil and gas
resources are actually present, the
location of wind resources relative to
consumers, future demand, economic
considerations, and environmental
regulations. Therefore, it is uncertain to
what degree energy projects will be
developed in mountain plover breeding
habitat in Wyoming, or other portions of
the range, in the foreseeable future.
However, given our evaluation above,
we believe that current and future
energy development in mountain plover
habitat may be substantial in Wyoming.
Existing and proposed oil and gas
development and wind energy projects
also occur in mountain plover habitat in
Montana and the plains of Colorado, as
well as in other States within the
mountain plover’s breeding, migratory,
and wintering range. The cumulative
total of current and future energy
development elsewhere in the mountain
plover’s breeding range may not
approach that likely to occur in
Wyoming, but energy development is
likely to occur within many breeding
areas used by the species. For example,
oil and gas development continues in
Weld County, Colorado, and renewed
exploration is occurring on and near the
PNG (Philbrook 2010, pers. comm.),
formerly an important breeding area for
the mountain plover.
Concerns over impacts of oil and gas
development to landscapes and to
various wildlife species have prompted
environmental review standards (BLM
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2010c), and may lead to more
widespread use of development
practices that minimize impacts. For
example, directional drilling, where
feasible, has the potential to decrease
habitat impacts. Increased piping,
product storage in central locations, and
remote sensing of wells may reduce
vehicular traffic and the impact of
roads.
Despite the prevalence of energy
development activities throughout the
range of the mountain plover, there is
little evidence as to whether, or to what
extent, the overall effects of energy
development are detrimental to
mountain plover (Andres and Stone
2009, p. 25). Although oil and gas field
development modifies and fragments
nesting, brood rearing, and foraging
habitats, mountain plover continue to
use these areas (Smith and Keinath
2004, p. 36; Carr, in review). For many
wildlife species, the principal impact of
energy development is fragmentation
rather than habitat loss. Energy
development, even when extensive, may
directly impact only a small percentage
of an area. In a study of the Big PineyLaBarge oil and gas field in the Upper
Green River Valley of Wyoming, where
well density averaged about one well
per 64 ac (26 ha), 97 percent of the
landscape was within 0.25 mile (0.40
kilometer) of infrastructure (roads,
pipelines, well pads, waste pits), but
only 4 percent of the area was directly
impacted by oil and gas infrastructure
(Morton et al. 2004, pp. 10–11). Carr (in
review) found that mountain plover
located nests in relation to habitat
available, rather than avoiding locations
of energy development. We have no data
to suggest that the mountain plover is
impacted by habitat fragmentation, as
opposed to habitat loss.
Because the mountain plover
generally favors disturbance that
reduces vegetative cover and exposes
bare ground (e.g., prairie dogs, grazing,
fire), it may tolerate surface disturbance
from energy development (Andres and
Stone 2009, p. 25; Carr, in review). In
Utah, disturbed areas around oil well
pads reportedly created open habitat
with bare ground suitable for the
mountain plover (Day 1994, pp. 298–
299). Manning and White (2001, p. 226)
found all mountain plover nests in Utah
to be situated near roadways or oil well
pads, and saw adults and chicks using
these areas for foraging both day and
night. However, they suggested that
while mountain plover tended to choose
nest sites near surface disturbance, the
overall impact of oil and gas expansion
could be negative (Manning and White
2001, p. 226). This small, apparently
isolated Utah population subsequently
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declined, and no birds have been found
during surveys of the area since 2003
(Maxfield 2010, pers. comm.). Decline of
the population occurred subsequent to
oil and gas development, but no direct
tie was established. Severe drought and
cessation of sheep grazing that provided
mountain plover breeding habitat may
have been more significant to the
apparent loss of this local population
(Maxfield 2010, pers. comm.).
Carr (in review) provides the only
targeted study of mountain plover
response to oil and gas development.
The USGS study evaluated the effects of
oil and gas development on mountain
plover population density and nesting
success in mixed desert shrublands in
Wyoming. Results suggested that the
presence of wells, roads, and associated
infrastructure at densities studied (up to
8 wells per square mile (3 per square
kilometer)) did not have detectable
negative effects on breeding mountain
plover (Carr, in review). Carr (in review)
concluded that energy development at
low to moderate levels may be
compatible with nesting mountain
plover, although the author suggested
the need for additional studies of
potential effects of energy development
on chick survival and potential for
impacts at higher well densities.
Tolerance to disturbance from energy
development by mountain plover could
result in nesting or foraging in areas
where continued human disturbance
and vehicular traffic could pose threats
to adults and chicks. Carr (in review)
cautioned that human activities at well
sites might keep mountain plover from
their nests, subjecting eggs to possible
overheating. In Oklahoma, mountain
plover appeared unaffected by the
presence of roads (MacConnell et al.
2009, p. 33). Manning and White (2001,
p. 226) indicated that vehicular traffic
did not influence incubation or foraging
behavior, and, while vehicular
collisions with mountain plover might
be a concern, no such mortalities were
noted. Andres and Stone (2009, pp. 26,
27) noted that mountain plover are
tolerant of vehicles, and while there is
potential that vehicles could kill adult
or juvenile birds, such mortality would
not likely have a population-level
impact. In addition, collisions with
stationary structures such as power
lines have been discounted as not likely
a significant cause of mortality (Knopf
and Wunder 2006; Andres and Stone
2009, p. 26).
Other impacts of energy development
on the mountain plover and its habitat
could occur. These include a potential
for increase in predators, increased
opportunity for spread of invasive
plants, and potential changes in human
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land use such as cessation of grazing.
Despite these concerns, to date, impacts
of oil and gas development at levels
typically seen in mountain plover
breeding habitat have not been shown to
decrease mountain plover populations.
Coalbed methane extraction is a
process in which: (1) Wells are drilled
into the coal seam; (2) the seam is
dewatered; and (3) the methane is then
extracted from the seam, compressed,
and piped to market. In Wyoming, some
water from coalbed methane operations
is used for surface or subsurface
irrigation of agriculture fields and
rangeland. There is concern that plover
habitat, including prairie dog colonies,
have been and could be lost to these
practices, thereby altering or eliminating
important mountain plover habitat
(Rogers 2010, pers. comm.). In the
Powder River Basin, about 2,000 ac (800
ha) of such irrigation is occurring and
more than 7,000 ac (3,000 ha) is
permitted (Fischer 2010, pers. comm.).
We have no information as to whether
or not mountain plover have been
displaced. While changes in habitat
caused by this irrigation may alter
habitat and cause a local impact to
mountain plover, we do not believe that
the relatively small area involved
represents a threat to overall mountain
plover populations in this region.
Like oil and gas development, wind
energy development presents a range of
habitat changes and disturbance factors
that could affect the mountain plover. In
addition, there is concern that the
mountain plover’s use of areas may
decline during and after construction
due to avoidance of wind turbines or
increased mortality attributable to
collisions, primarily with moving rotor
blades. Lock (2010) highlighted the
potential for wind energy projects to
displace breeding mountain plover, but
described the potential threat of
mortality from collisions as being of
‘‘low certainty.’’
The most comprehensive study
conducted on potential effects of wind
power development on the mountain
plover came from the facility on Foote
Creek Rim in Carbon County, Wyoming,
where mountain plover were studied
from 1994 (prior to construction)
through 2007 (Young et al. 2007, entire).
The authors suggested that mountain
plover habituated over time to the
presence of turbines, as evidenced by
nesting within 60 feet (ft) (20 meters
(m)) of the base of a tower in one
instance (Young et al. 2007, p. 18).
Wind towers, rotors, and associated
meteorological towers pose an added
risk that mountain plover may be struck
by blades or fly into stationary
structures. However, carcass searches at
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Foote Creek Rim documented no
mountain plover mortalities attributable
to collisions over the 3 years the studies
were conducted. On breeding grounds,
mountain plover fly at low heights. In
a common courtship display, a male
flies only to a height of approximately
16 to 33 ft (5 to 10 m) (Knopf and
Wunder 2006). The lowest point of rotor
sweep on the Foote Creek Rim site (57
ft (17 m)) was above the typical heights
flown by mountain plover during
courtship and breeding (Young et al.
2007, p. 18). Research at the Judith Gap
Wind Farm in Montana found no
evidence of mountain plover
displacement or fatalities (MacDonald
2010). However, recently we became
aware of two mountain plover
mortalities from searches of Wyoming
wind energy projects (Sweanor 2010,
pers. comm.). Because sources of
mortality could not be confirmed for
either carcass, we do not know whether
the birds were struck by rotor blades,
collided with towers, or died from other
causes. Rotor sweep was 126 ft (41 m)
above the ground in both cases, well
above heights that breeding mountain
plover are thought to regularly fly. At
Glenrock Rolling Hills, one of the two
sites reporting a mortality, no mountain
plover were observed prior to
construction of the wind energy project,
but nesting occurred after construction,
suggesting that nesting habitat may have
been created through project
disturbance (Sweanor 2010, pers.
comm.).
Wind energy development could
present a greater potential issue for postbreeding congregations of mountain
plover, because hundreds of birds may
flock in a single area. However, we have
no information regarding behavior of
post-breeding flocks that could be
applied to the potential threat of bird
strikes from wind turbines. Little is
known regarding their potential to strike
moving blades or stationary structures,
although based on mortality studies,
shorebirds (plovers, sandpipers, and
similar species) do not seem to be at
great risk of colliding with turbines or
communication towers (Kerlinger 2011,
pers. comm.). Wind energy projects
have reportedly been constructed and
are proposed in South Texas
agricultural fields that may overlap with
areas used by wintering mountain
plover (Cobb 2010, pers. comm.). The
potential for mountain plover
displacement or collisions in Texas is
unknown. In California, wind energy
development projects tend to be located
on mountain ridges where wind speeds
are greater and, therefore, are less likely
to impact wintering mountain plover.
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One exception is in Antelope Valley,
Kern County (California), an area where
mountain plover are known to winter.
Several wind energy projects have been
permitted on a mosaic of desert and
agricultural lands. Overall, evidence
available does not suggest that wind
energy development is likely to displace
mountain plover from breeding or
wintering areas, or cause direct
mortality through collisions to the
extent that it would pose a threat to the
species.
Surface mining for coal and other
minerals can displace mountain plover
within the footprint of the work for the
duration of the active mining. Whether
or not this would result in permanent
displacement is dependent on whether
and how restoration occurs. We have
little site-specific data on impacts of
surface mining to nearby mountain
plover. Surveys over 28 years at Cloud
Peak Energy’s Antelope Mine in
Campbell and Converse Counties,
Wyoming, documented mountain
plover’s use of the mine permit area and
adjacent lands (Green 2010). Mountain
plover numbers declined as mining and
the footprint of surface disturbance
progressed, but in general they showed
tolerance to mining activities nearby
(Green 2010). In 2010, adult mountain
plover and chicks were, for the first
time, seen using a reclaimed mine area
at the Antelope Mine (Green 2010).
Mountain plover can be directly affected
by surface mining through temporary or
permanent loss of their habitat.
However, we do not believe that surface
mining, currently or in the future, will
impact a significant amount of the
mountain plover’s breeding range or
represent a threat to the species.
The BLM considers the mountain
plover, among other species, when
evaluating the impacts of energy
development on the environment. The
BLM, through its Special Status Species
program, has developed various
management scenarios for the protection
of the mountain plover throughout its
range. In 2005, the BLM analyzed the
potential effects to the mountain plover
from management actions approved in
Resource Management Plans for the
various BLM field offices in Wyoming
(BLM 2005). At the time, we concluded
that BLM’s proactive conservation
measures should aid in protecting the
species from further decline (Kelly
2007). The conservation measures
committed to by the BLM included
habitat screening (determining whether
habitat might support the mountain
plover) and, as appropriate, subsequent
surveys for the possible presence of
mountain plover prior to approval of
ground-disturbing activities; designation
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of a 0.25-mi (0.40-km) buffer around
occupied nests during the nesting
season, with restrictions on activities to
protect nesting plover; and continued
research and census activities targeting
the mountain plover on BLMadministered land in Wyoming (BLM
2005). A number of best management
practices were also provided, to be
considered on a case-by-case basis, to
help protect the mountain plover and
expand suitable nesting habitat. While
these measures are not binding, and onthe-ground conservation efforts likely
vary by BLM field office, a proactive
cooperative approach between the BLM
and the Service in Wyoming has
heightened recognition of mountain
plover conservation on BLMadministered lands and provides a basis
for future cooperation to safeguard the
species.
Solar energy projects are likely to
displace mountain plover when situated
in breeding or wintering habitat. Unlike
oil and gas wells or wind turbines, solar
collectors are placed so close together
that they effectively eliminate the ability
of mountain plover to use the habitat.
Solar energy development potential is
greatest in southwestern States and
California and, except for Colorado’s
San Luis Valley and Northern New
Mexico, occurs in areas used mostly by
wintering rather than breeding
mountain plover. See Changes in Land
Use in Mountain Plover Wintering
Range below for a discussion of solar
energy development.
In summary, potential effects to the
mountain plover from energy and
mineral development are largely
uncertain. Ground disturbance from oil
and gas development and wind energy
development may, in some cases,
enhance or create mountain plover
habitat, but whether the net effect of
such activity is beneficial or detrimental
has not been determined. The risk of
significant mortality through mountain
plover being struck by rotors of wind
turbines appears low. Whether, or to
what extent, construction of wind
energy projects displaces breeding or
wintering mountain plover has not been
clearly established. Surface mining
displaces mountain plover, at least until
an area is restored, and development of
solar fields likely results in habitat loss.
Overall, more information regarding
possible impacts of energy and mineral
development to mountain plover is
needed. However, the information
currently available does not indicate
that energy and mineral development
threatens the mountain plover now or is
likely to do so within the foreseeable
future.
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Changes in Land Use in Mountain
Plover Wintering Range
In our December 5, 2002, proposal to
list the mountain plover (67 FR 72396),
we emphasized the potential impact to
mountain plover populations from
changes to wintering habitat in
California, including changes stemming
from human population growth,
changes in agriculture, water
availability, and burning restrictions. It
now appears that the proportion of the
rangewide population of mountain
plover that winter in California is far
less than previously believed (see
Conservation Status and Local
Populations above). However, the
importance of mountain plover
wintering habitat in California has been
a continued topic of investigation and
interest (Kopft and Rupert 1995;
Hunting et al. 2001; Wunder and Knopf
2003; Hunting and Edson 2008). Knopf
and Rupert (1995, p. 750) cited a high
overwinter survival rate of mountain
plover in California and their use of
agricultural fields, and concluded that
long-term population declines were
likely attributable to processes on their
breeding grounds. Dinsmore et al.
(2010) concluded that adult survival in
winter was high and suggested that
conservation and management efforts be
directed toward chick survival on
breeding grounds and habitat during
migration. In contrast, Hunting and
Edson (2008, p. 184) attributed both past
declines and potential future declines in
rangewide plover populations to loss of
traditional wintering sites in California.
Andres and Stone (2009, pp. 21, 22)
stated that effects to the mountain
plover from changes to wintering habitat
in California’s Central Valley were
unknown, but also expressed concerns
regarding maintenance of quality
wintering habitat in the Imperial Valley,
where a majority of mountain plover in
California are now thought to winter.
Below we address current trends and
potential changes to the future extent
and quality of mountain plover
wintering habitat in California.
Concern continues to center on land
use trends, conversion of agricultural
lands to other uses, and changes in
agriculture (Andres and Stone 2009, pp.
22–24; Hunting and Edson 2008, p.
184). Due to population growth in
California, more rural and agricultural
land is being urbanized. Between 1982
and 2007, approximately 8 percent of
California’s croplands, 11 percent of the
State’s pasturelands, and 6 percent of
State’s rangelands were lost (USDA
2010). However, as of 2007, California
still supported approximately 9.5
million ac (3.8 million ha) of cropland,
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1.1 million ac (0.4 million ha) of
pastureland, and 17.5 million ac (7.0
million ha) of rangeland (USDA 2010).
The dynamic, market-driven nature of
agricultural production and changes in
cultivation practices in California could
affect the availability and quality of
wintering habitat for the mountain
plover. Another issue is the dependence
of California agriculture on irrigation
water, some of which is imported from
other areas, and its future availability.
Future changes in the availability of
irrigation water might result from
competition with other water uses, the
effects of global climate change (see
discussion under Factor E below), and
changes in the characteristics of
agricultural lands as a result of
improved or more broadly implemented
water conservation techniques.
Development of energy projects,
especially solar energy, in mountain
plover wintering habitat is also a
concern in California. California’s
electric utility companies were required
by California statute (Chapter 464,
Statutes of 2006) to use renewable
energy to produce 20 percent of their
power by 2010. Governor
Schwarzenegger’s Executive Order of
November 2008 (#S–13–08) set a higher,
more ambitious goal of 33 percent by
2020 (California Energy Commission
2010). On April 12, 2011, Governor Jerry
Brown signed Senate Bill 2X into law,
requiring that 33 percent of the State’s
electric generation come from renewable
sources by 2020 (Los Angeles Times
2011). A main source of renewable
power will be solar energy. A Statewide
list of solar energy projects includes
over 400 proposals (Brickley 2011, pers.
comm.). Many large solar energy
projects are being proposed on BLM
land, often in desert areas. The BLM,
along with the Department of Energy
(DOE), is currently in the process of
developing a Programmatic
Environmental Impact Statement (PEIS)
for solar energy development in six
southwestern States, including
California. The document assesses
development of a new solar energy
program for siting utility-scale solar
energy projects on BLM lands. Any
program adopted will have implications
for solar energy project siting in
mountain plover wintering habitat. A
draft of the PEIS was made available for
public comment December 17, 2010 (75
FR 78980). Mountain plover are not
specifically addressed in the PEIS, but
potential impacts to wildlife and
appropriate mitigation measures are
provided (DOE 2010, pp. 5–73 to 5–96).
As described in Conservation Status
and Local Populations above, the
California winter range of the mountain
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plover is primarily in the Central Valley
(including the Sacramento and San
Joaquin valleys) and the Imperial
Valley. The Carrizo Plain in San Luis
Obispo County is also recognized as an
important wintering site. Other areas
where mountain plover are regularly
observed include the Panoche and
Antelope valleys.
The Central Valley (Sacramento Valley
and San Joaquin Valley), Carrizo Plain,
Panoche Valley, and Antelope Valley
In the Central Valley, human
population growth over the last 20 years
has resulted in a declining trend in
agricultural area, with a smaller, but
corresponding, trend of conversion to
urban uses (California Department of
Conservation (CDC) 2010). The rate of
land conversion to urban uses in the
Central Valley increased beginning in
1990. With the exception of Solano
County, the human populations of
Central Valley counties within the
wintering range of the mountain plover
all grew faster than the Statewide
average between 2000 and 2009 (U.S.
Census Bureau 2010).
In the Sacramento Valley,
urbanization in Yolo and Solano
Counties, the two principal counties
supporting wintering mountain plover,
has not adversely impacted the
mountain plover to date, because known
wintering locations are located outside
city planning boundaries. However,
continued population growth beyond
the current planning horizon could
potentially threaten individual
wintering localities that are close to
urban areas, particularly those in areas
most proximate to Sacramento.
In the San Joaquin Valley, human
population growth has been
approximately 17 percent over the
period from 1997 through 2010. To date,
most of the resulting urban growth has
occurred adjacent to, and in the general
vicinity of, the towns, such as Modesto,
Fresno, and Bakersfield, that developed
along Highway 99 in the eastern portion
of the San Joaquin Valley (Teitz et al.
2005, p. 27). These urban areas are
located to the east and outside of the
mountain plover’s wintering range. To
date, urbanization in the western San
Joaquin Valley is restricted to the
Interstate 5 corridor, which supports
few mountain plover. Therefore, we
expect it to have little effect on
wintering mountain plover. Scenarios
developed to gauge effects of future
population growth and urbanization
suggest that the San Joaquin Valley will
experience significant urban growth
within the next 35 years; increasing
populations will result in scattered
urbanization within the plover’s
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wintering range, but the pattern of
development will depend on land use
planning goals, and potential
development of high speed rail (Teitz et
al. 2005, pp. 45–67).
In the San Joaquin Valley counties
(Fresno, Kern, Kings, Madera, Merced,
San Joaquin, Stanislaus, Tulare),
cropland declined by about 3 percent
from 1997 to 2007, to about 5.2 million
ac (2.1 million ha) (USDA 2010). Crop
fields in alfalfa and other hay, favored
by mountain plover, were relatively
stable and accounted for about one-third
of all cropland in the San Joaquin Valley
in 2007 (USDA 2010).
While relatively little agricultural
land is being lost, conversion from
annual agricultural crops to permanent
crops that do not provide mountain
plover with habitat is significant within
the San Joaquin Valley. For example, in
the San Luis Unit of the Central Valley
Project (CVP), in Fresno, Kings, and
Merced Counties, agricultural acreage
has increasingly been converted to
permanent crops of orchards or
vineyards. We estimate the percentage
of land in permanent crops at
somewhere between 16 percent and 24
percent of the San Luis Unit, compared
with 10 percent in 2000. General field
observations and land value reports
(California Society of Farm Managers
and Rural Appraisers 2009, pp. 31–64)
suggest that this is a continuing trend,
with new orchards displacing cotton
and tomato crops in many areas of the
Central Valley. In Madera County, some
locations formerly utilized by wintering
mountain plover have been converted
from rangeland to annual crops or to
permanent crops such as pistachio trees
(Woods 2009, pers. comm.).
Outside of the Central Valley, orchard
land in San Luis Obispo County, which
includes the Carrizo Plain, a known
mountain plover wintering area, rose
from 29,000 ac (12,000 ha) to 54,000 ac
(22,000 ha) from 2007 to 2009, to about
18 percent of cropland in the county.
Conversion to orchard crops in the
nearby Maricopa and Cuyama valleys
near the Carrizo Plain area have resulted
in loss of wintering mountain plover
habitat (Sharum 2010). Overall,
conversion of annual cropping systems
to permanent crops is expected to
continue and poses an additional, but
unquantified, source of habitat loss for
the mountain plover.
As a result of the large-scale irrigation
efforts in the western San Joaquin
Valley, approximately 1,750,000 ac
(710,000 ha) of agricultural lands with
shallow groundwater tables have
become impaired due to accumulated
concentrations of naturally occurring
toxic elements, including selenium.
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With the passage of the Central Valley
Project Improvement Act (CVPIA) in
1992, Federal and State acquisition
programs enabled owners to stop
farming, or ‘‘retire’’ their privately
owned, drainage-impaired agricultural
lands as a strategy to reduce drainage
problems and address selenium
accumulations (Service 1998; USDI
2005). Lands targeted for retirement lie
primarily within the San Luis Unit of
the CVP along the west side of the San
Joaquin Valley where approximately
379,000 ac (152,000 ha) of agricultural
land have been identified as
contributing to poor water quality. Of
these lands, nearly 200,000 ac (80,000
ha) have been proposed for land
retirement (USBR 2007), and, to date,
more than 100,000 ac (40,000 ha) of
agricultural land have been retired
within the San Luis Unit. We have no
estimate of what proportion of this area
may have supported acceptable
wintering habitat for the mountain
plover or the extent to which it was
used by the mountain plover.
A portion of the lands proposed for
retirement are expected to be used for
drainage reclamation; between 1,280
and 3,300 ac (5,170 and 1,340 ha) of
existing irrigated cropland will be
converted to treatment facilities and
evaporation basins, while 12,500 ac
(5,100 ha) of either existing or fallowed
cropland will be converted to reuse
areas in which crops will be irrigated
with selenium-contaminated,
agricultural drainwater in order to
reduce selenium loads in the
agricultural run-off (Service 2006).
These areas might threaten some
mountain plover with selenium toxicity,
as described below in the discussion
under Factor E. Numerous retired
parcels are characterized by dense
weedy growth (Cypher et al. 2007, p. 28;
Service 2006), and are not expected to
provide suitable habitat for the plover.
Substantial retired acreage has been
converted to permanent crops utilizing
alternate sources of water. Other retired
lands that support grazing or farming
may remain suitable for wintering
mountain plover.
Due to the historical importance of
agriculture in the Central Valley, the
valley has the highest percentage of
privately owned land in the State. Only
4 percent of Sacramento Valley land and
7 percent of San Joaquin Valley land is
public open space. In the Central Valley,
a variety of conservation and restoration
projects have been implemented to
protect natural resources, although 57
percent of such conservation projects
report a focus on riparian habitat
enhancement (Great Valley Center 2005,
p. 30). Twenty-three local and regional
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land trusts operate in the Central Valley
to protect valley wildlife, farmland,
habitat, rivers, and native vegetation
(Great Valley Center 2005, pp. 30–31).
The Service does not have information
on the area of specific habitat types that
have been protected within the range of
the mountain plover or whether these
efforts have produced substantial
benefits to the species.
In the Sacramento Valley, we have
found no planned solar energy
development likely to threaten the
mountain plover’s habitat. However, the
legislation cited above (Chapter 464,
Statutes of 2006, and Governor
Schwarzenegger’s Executive Order of
November 2008 (#S–13–08)) has
initiated a significant increase in the
planning for solar development in and
adjacent to the San Joaquin Valley. Solar
developments proposed thus far vary
greatly in size: small projects of 100 to
200 ac (40 to 80 ha), to projects of
potentially to 30,000 ac (12,000 ha) in
size. The Service does not have specific
information on mountain plover use of
many of these sites, but we conclude
that sites will be unsuitable for
mountain plover after development.
To date, small projects are proposed
for scattered locations across the
southern San Joaquin Valley, while
large projects have been proposed both
within the San Joaquin Valley, and in
the Carrizo Plain and Panoche Valley
areas. The solar projects proposed on
the valley floor are typically situated on
active or recently cultivated agricultural
lands and several larger projects have
been proposed for lands that have been
used for livestock grazing.
The Service is currently aware of up
to six small solar projects, each
approximately 200 ac (80 ha) in size,
which are expected within the
mountain plover’s general wintering
range in the southern San Joaquin
Valley. The projects will be constructed
by Pacific Gas and Electric, a major
California utility company. In the San
Joaquin Valley, the solar projects
proposed on the valley floor are
typically situated on active or recently
cultivated agricultural lands and several
larger projects have been proposed for
lands that have been used for livestock
grazing. The Service concludes that sites
will be unsuitable for mountain plover
after development.
Several large proposals are located
within the mountain plover’s general
wintering range. A large 32,000-ac
(13,000-ha) park, the Westlands Solar
Park, has been proposed for western
Fresno and Kings Counties, with an
initial phase of approximately 10,000 ac
(4,000 ha). It will be constructed on
agricultural land that the Westlands
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Water District has slated for land
retirement (Woody 2010). We expect
that additional proposals for retired
farmland are likely due to the general
perception that such lands have few
environmental issues.
The Maricopa Sun Solar Complex
(approximately 9,000 ac (3,600 ha)) is
proposed for agricultural lands in
western Kern County near the edge of
the plover’s winter range. We do not
know whether the mountain plover uses
the site. Development of the project
includes cancellation of a contract to
preserve agricultural land. The Draft
Environmental Impact Report identifies
mountain plover as a potential winter
migrant (Kern County Planning and
Community Development Department
2010, pp. 1, 4.4–8).
In the Carrizo Plain, San Luis Obispo
County, two solar projects have been
proposed, including the 4,000-ac (1,619ha) California Valley Solar Ranch
(CVSR) and the 4,500-ac (1,800-ha)
Topaz Solar Farm. Both facilities would
be located approximately 6 miles north
of the Carrizo Plains National
Monument, an important natural area
for the plover, on a mixture of natural
lands, grazing lands, and cropped lands
(Aspen Environmental Group 2010, pp.
C3–2–C3–3, C6–4). Suitable foraging
and roosting habitat for the mountain
plover occurs on sites under
consideration (Aspen Environmental
Group 2010, pp. C6–4–C6–5, C6–11).
Mountain plover have been observed on
the CVSR site but likely occur
sporadically and in low numbers
(Boroski 2011, pers. comm.).
The Panoche Valley, an area of about
12,000 ac (5,000 ha) in San Benito
County, receives annual use by
wintering mountain plovers. A solar
project is currently proposed on 3,200
ac (1,300 ha) of potential mountain
plover wintering habitat, or about onethird of the potential mountain plover
habitat present in the Panoche Valley.
Proposed mitigation would preserve and
manage other nearby habitat.
The Antelope Valley, an area of
approximately 900,000 ac (360,000 ha)
in Los Angeles and Kern Counties,
supports wintering mountain plover
annually, with numbers estimated in the
low 100s using crop fields and
grasslands (eBird 2010). How much of
the valley’s area is mountain plover
habitat is unclear. The valley is
primarily privately owned land, and its
proximity to human population centers
has generated high interest in renewable
energy (solar and wind) development
that could reduce mountain plover
wintering habitat.
Solar energy projects currently
planned in the San Joaquin Valley, the
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adjacent Carrizo Plain, and the Panoche
and Antelope valleys are likely, over
time, to reduce existing mountain
plover wintering habitat. A variety of
siting considerations, including
presence of other wildlife species of
concern, and potential mitigation
requirements, will dictate the extent to
which mountain plover are affected.
The Sacramento Valley and Imperial
Valley lands used by the mountain
plover are less likely to be developed for
solar projects. We know of no solar
projects are currently planned for
agricultural lands known to support
mountain plover in the Imperial Valley,
discussed below.
As future solar projects are proposed
and implemented, we conclude that
they will cause some continued loss of
mountain plover wintering habitat in
California. While cumulative impacts of
these projects, and other factors such as
urbanization and changes in agriculture,
are likely to reduce the total area of
wintering habitat available, substantial
acreage of appropriate wintering habitat
will persist in the Central Valley,
Carrizo Plain, Panoche Valley, and
Antelope Valley.
The Imperial Valley
As of 2009, about 381,000 ac (154,000
ha) of field crops existed in the Imperial
Valley (Imperial Irrigation District (IID)
2009a). The Imperial County has
witnessed a decline in annual area used
for agricultural purposes from 1984
through 2008 of about 21,000 ac (8,000
ha) or 4 percent (CDC 2010), while the
county saw an increase in area used for
urban areas in the same period of about
6,000 ac (2,400 ha) or 29 percent (CDC
2010). Urban expansion has accounted
for only a relatively small portion of the
4 percent decline in agricultural lands
over a period of 24 years. At this rate,
conversion of agricultural lands to
urban lands in Imperial County has a
modest impact.
Habitat in the Imperial Valley
believed most important for mountain
plover includes alfalfa fields, especially
those harvested then grazed by sheep,
and bermudagrass fields burned
following harvest (Wunder and Knopf
2002, pp. 75–76). Both alfalfa and
bermudagrass acreages have declined in
recent years (2005–2009) (IID 2009a).
However, in 2009, these crops occupied
195,000 ac (79,000 ha) or approximately
51 percent of total field crop acreage in
the Imperial Valley (IID 2009a). Area
devoted to all hay (including alfalfa and
bermudagrass), 233,000 ac (90,000 ha),
was the same in Imperial County in both
1997 and the 2007 (USDA 2010). Data
available also suggest the number of
sheep in the Imperial Valley have
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declined recently as well but that
numbers fluctuate over time. It is not
known whether these short-term
declines are indicative of future trends.
The continued success of agricultural
habitats used by the mountain plover in
the Imperial Valley depends on a
reliable water supply. The Imperial
Valley depends on Colorado River water
to irrigate its crops, but there has been
increasing pressure for more water to be
diverted to urban areas. In 2003, the
State of California and water agencies
across the State signed the
Quantification Settlement Agreement
(QSA) to dictate distribution of water
from the Colorado River. The settlement
allocated 370,000 acre-feet (ac-ft) (456
million cubic meters (cu-m)) of water to
urban areas in Southern California and
Tribal areas (IID 2010a, p. 2). Most of
the 370,000 ac-ft (456 million cu-m) will
come from improvements in on-farm
water efficiency and improved irrigation
technology (IID 2010a, p. 2; Delfino
2006, p. 161).
Under the QSA, Imperial County must
also fallow agricultural land, some of
which will be transferred to the San
Diego Water Authority, and some of
which will go to mitigation to restore
the Salton Sea (IID 2010a, p. 1). The area
of land fallowed depends on the
intensity of water use, not farm size (IID
2010b, p. 1). Fallowing will be
conducted on a sliding scale. The
program began in 2003 with lands
fallowed that had been irrigated by
under 10,000 ac-ft (1.2 million cu-m) of
water, and peaked in 2010 to lands
fallowed that had been irrigated by over
80,000 ac-ft (9.9 million cu-m) of water.
The program will slowly decline before
agricultural fallowing ends in 2017 (IID
2009b). The area of land fallowed in
2009–2010 was about 10,500 ac (4,300
ha) or about 2 percent of agricultural
land in the valley. Overall, lands
fallowed will reduce the area of crop
fields in the Imperial Valley but we
have no specific information as to extent
to which those fields fallowed provide
wintering habitat to the mountain
plover.
The future of the QSA is in question.
On January 13, 2010, the Superior Court
of California found that funding
provisions of the QSA were
unconstitutional, and officially
invalidated the QSA on January 19,
2010 (QSA Coordinated Cases, Case No.:
JC4353). IID asked for, and received, a
stay that temporarily allowed the terms
of the QSA to remain in effect (Case No.:
JC4353). As of April 2011, a ruling was
anticipated before the end of the year
(Imperial Valley Press 2011, p. 1). It is
unclear what effect the cancellation of
the QSA will have on water use and
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fallowing, given the extreme contention
and difficulty in negotiating the 2003
settlement. If the stay does not remain
in place, the IID may halt fallowing, as
it has been strongly opposed to
fallowing as a conservation measure (IID
2010c, p. 1). If the fallowing program
remains in place, it could continue as an
immediate, but relatively insignificant,
threat to mountain plover habitat, as it
would only affect a small portion of
agricultural fields, with no definitive
data indicating if (or how much)
fallowing will occur on those croplands
that mountain plover frequent.
The yield from alfalfa crops is related
to the amount of irrigation the land
receives (Hanson et al. 2007, p. 1).
Alfalfa could thus be more significantly
impacted by water use restrictions. In
California, revenue for alfalfa is
expected to decrease slightly by 2050,
decreasing 11 percent Statewide (Howitt
et al. 2008, p. 11). These statistics take
water use into consideration (California
Department of Finance 2007, p. 5). In
contrast, Bermudagrass is droughttolerant, and one study showed little
decrease in crop yield under drought
conditions (Kneebone 1966, p. 96;
George et al. 1992, pp. 23–24).
Yield and acreage of bermudagrass
could be affected by restrictions on
burning in the Imperial Valley due to
pollution concerns. To comply with
California’s air pollution restrictions
(California Code of Regulations 2001,
pp. 80100–80170), the Imperial County
Air Pollution Control District (ICAPCD)
has set forth rules and regulations
(ICAPCD 2010b, pp. 701.1–702.1)
governing implementation of a smoke
management program (ICAPCD 2010a,
pp. 1–37) for agricultural burning. These
rules and regulations allow for
agricultural burning after the ICAPCD
has analyzed several factors: (1)
Quantitative and qualitative analysis of
meteorological conditions; (2) current
smoke complaints; (3) source/receptor
consideration; and (4) current air quality
levels (ICAPCD 2010b, p. 8). The
number of burn days permissible in the
areas of Imperial County has declined
(California Air Resources Board 2010)
since 2003, but the amount of
bermudagrass acreage burned in the
same period (2003 to 2009) shows little
trend and averages about 18,000 ac
(7,000 ha) (Lancero, pers. comm.;
Cavazos 2010, pers. comm.). Any
concern that current burning restrictions
limit bermudagrass cultivation appears
unsupported by these data.
Future trends in alfalfa and
Bermudagrass may largely determine
the extent and quality of mountain
plover wintering habitat available in the
Imperial Valley. While no predictions of
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future area devoted to these two crops
is available, we do not have any
information that would lead us to
conclude that their occurrence will
significantly decline. Therefore, we
anticipate that in the future substantial
areas of alfalfa and Bermudagrass fields
will remain available to support
wintering mountain plover in the
Imperial Valley.
Currently, there is no habitat
conservation plan (HCP) implemented
in the Imperial County. The Imperial
Irrigation District is currently working
on an HCP, but they have not yet
finalized the plan or been issued a
section 10(a)(1)(b) permit under the Act
(Roberts 2010, pers. comm.); however,
in the current draft of the HCP,
mountain plover is a covered species.
Individually, urbanization, water
restrictions, and trends in agriculture do
not appear to pose significant threats to
the acreage or quality of wintering
habitat available or to the mountain
plover’s use of the Imperial Valley.
However, in the foreseeable future, their
combined effects, along with climate
change, could appreciably reduce
habitat available to mountain plover and
potentially affect the nature or extent of
wintering mountain plover use of the
Imperial Valley.
Mountain plover winter over a large
range and in diverse habitats. In our
February 16, 1999, proposed rule to list
the species we cited sources suggesting
that most mountain plover, an estimated
7,000 of a rangewide population of
8,000 to 10,000 birds, wintered in
California (64 FR 7587). However, we
now believe that less than half of the
rangewide population, estimated at over
20,000 birds, winter in California (see
Population Size and Trends above). As
of 2007, over 18 million ac (7 million
ha) in California (about 18 percent of the
State) supported cropland, pastureland,
or rangeland (USDA 2010). While only
a portion of this area provides habitat
for the mountain plover in any given
winter, the total includes 1.7 million ac
(0.7 million ha) of alfalfa, Bemudagrass,
and other hay crops that the mountain
plover utilizes, including 230,000 ac
(90,000 ha) in Imperial County alone.
The total also includes 1.1 million ac
(0.4 million ha) of pastureland, often
used by mountain plover. To exploit
these and other wintering habitats,
mountain plover are able to move long
distances and use various sites as
conditions become favorable within a
given winter (Knopf and Wunder 2006).
Mountain plover appear annually at
some favored wintering sites, but site
fidelity by individual birds appears low.
Birds may also alternate between
wintering areas in California and
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elsewhere in different years.
Cumulatively, the potential changes in
land uses in California described above
will likely result in a reduction of
mountain plover wintering habitat in
the State. However, given the available
agricultural acreage cited above, it is not
apparent that even a reduction in
California wintering habitat
substantially larger than that which we
anticipate would significantly affect
California’s ability to support mountain
plover numbers currently wintering in
the State. We conclude that any likely
reduction of mountain plover wintering
habitat in California will not threaten
the mountain plover plover’s ability to
maintain a wintering population in
California or threaten the species range
wide in the foreseeable future.
Other than potential impacts from
wind energy development described in
Energy and Mineral Development above,
we have no information regarding
threats to wintering mountain plover
from habitat changes in Texas.
Outside of the trends in wintering
areas in Mexico described in Threats to
Prairie Dogs and Associated Loss of
Habitat above, we have little
information regarding threats to the
mountain plover from wintering habitat
changes in Mexico. Based on their
wintering habitat preferences in the
United States, significant numbers of
mountain plover may winter in
agricultural areas in Mexico. Possible
areas of concentration and the types of
agriculture utilized remain
undocumented.
Wintering Outside of California
Summary of Factor A
The mountain plover occupies a wide
geographic range across the breeding,
migration, and wintering seasons. The
extensive and diverse habitats it utilizes
are subject to a number of changes that
represent potential threats.
Black-tailed prairie dogs create
favorable breeding habitat for the
mountain plover in States including
Colorado, Montana, and Wyoming.
Black-tailed prairie dog numbers have
increased by a factor of six since 1981
in States where they are present, and
associated mountain plover habitat has
likewise increased. We do not anticipate
loss of black-tailed prairie dog numbers
or the mountain plover habitat they
maintain in the foreseeable future.
Current conversion of prairie and
grasslands to other land uses within
mountain plover breeding habitat
appears negligible when viewed from a
rangewide perspective. Formerly
expressed concerns regarding human
development in South Park, Colorado,
where a high density of mountain
plover breeds, now seem unfounded.
Cattle grazing generally benefits
mountain plover breeding habitat, but
some range management practices do
not create favorable conditions for
mountain plover breeding. Specific
range management to benefit mountain
plover could be employed, but overall
we expect current cattle grazing to
continue relatively unchanged in the
foreseeable future.
Suggestions that cropland use by
breeding mountain plover may be
detrimental to populations have not
been substantiated.
Energy and mineral development
alters landscapes, and some activities
can adversely impact mountain plover
habitat, at least locally and temporally.
The mountain plover often benefits from
ground disturbance and may tolerate or
Elsewhere, in the Phoenix area,
Maricopa County, and some other
wintering sites in southern Arizona,
mountain plover have been displaced by
growth of human populations (Gardner
2010; Robertson 2010, pers. comm.).
Declines are likely to occur in the
Tucson area, Pinal County, and perhaps
in Yuma County as well, due to
increased human populations and, more
directly, due to an accompanying
reduction in agriculture. Wintering
mountain plover populations in Cochise
County, where there is less urban
development and where the amount of
cropland increased from 1997 to 2007
(USDA 2010), will likely remain more
stable. Solar energy development is
occurring in areas of southern Arizona,
but the extent to which projects may
overlap mountain plover wintering
habitat has not yet been determined.
Both increases in human population
and expansion of agriculture are
occurring in areas of southern Arizona
(Council for Agricultural Science and
Technology 2009, pp. 8–12). Rather than
the total area urbanized, the extent and
nature of future agriculture that is
present in southern Arizona and
available for mountain plover use will
likely dictate the future value of this
area to wintering mountain plover.
However, water resources are limited,
and urban uses may compete with
agriculture for available water. Southern
Arizona is thought to winter a relatively
small portion of the rangewide
mountain plover population. We believe
that any net future decreases in
agricultural lands in southern Arizona
will be limited and that these potential
future decreases in agricultural lands in
southern Arizona will not markedly
affect the ability of the area to support
these wintering mountain plover.
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benefit from certain development
activities. Mountain plover collisions
with wind turbines are likely to occur
infrequently. Overall, oil and gas
extraction, wind power projects, and
mineral extraction have not been shown
to have significant adverse impacts to
the mountain plover.
Wintering mountain plover are wideranging, and seek out a variety of
grassland, rangeland, crop field, and
semi-desert landscapes, from the Gulf
Coast to the Pacific Ocean, to meet their
needs. Habitat in California and across
the mountain plover’s wintering range is
dynamic, based on yearly weather
patterns, grazing levels, crops present,
and timing of planting or harvest.
Currently available wintering habitat
can not be easily quantified, nor can its
projected quantity and quality in the
foreseeable future be easily predicted. A
future net loss of wintering habitat in
California appears likely, based on solar
development projects and other factors
described above, but given the expanse
of wintering habitat currently present, it
is not apparent that this will have any
affect on the number of wintering
mountain plover California will
support.
Dinsmore et al. (2010) assessed factors
affecting population growth in the
mountain plover in order to target
conservation and management efforts.
They cited mountain plover adult
survival as high in winter and suggested
conservation efforts should target
increased chick survival on breeding
grounds. This is consistent with Knopf
and Rupert (1995, p. 750), who
concluded that past declines in the
mountain plover were attributable to
events taking place on the breeding
grounds not during winter. We believe
that rather than changes in wintering
habitat, future changes on the mountain
plover’s breeding grounds that influence
reproductive success will dictate
rangewide mountain plover numbers
and population trends. The quantity and
quality of breeding habitat, and the
ability of the mountain plover to
successfully reproduce will depend
largely on future human land uses,
rangeland and cropland management
practices, the potential effects of energy
development, and the abundance and
distribution of prairie dogs. We have no
credible evidence to show that future
changes in the extent and quality of
mountain plover rangewide wintering
habitat, of the magnitude likely to occur,
would significantly influence their total
population or population trend, or that
they endanger the species now or would
be likely to endanger the species in the
foreseeable future.
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We conclude that the best information
available indicates that the mountain
plover 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.
will become a threat to the species in
the foreseeable future. We conclude that
the best scientific and commercial
information available indicates that the
mountain plover is not now, nor in the
foreseeable future, threatened by
overutilization for commercial,
recreational, scientific, or educational
purposes.
Factor B. Overutilization for
Commercial, Recreational, Scientific, or
Educational Purposes
Mountain plover were historically
hunted for human consumption on the
Great Plains (Knopf and Wunder 2006).
Under the Migratory Bird Treaty Act
(MBTA) (16 U.S.C. 703–712), mountain
plover are not legally hunted in the
United States, Canada, or Mexico,
although Andres and Stone (2009, p. 27)
note that some illegal shooting may
occur in some areas of Mexico. The
extent or significance of any such
activity is unknown, but, because we
have no information that such illegal
hunting activity is widespread, we
believe it is unlikely to be a significant
threat to the mountain plover’s
continued existence.
Birders (bird watchers) may seek out
mountain plover for viewing. This
activity is most likely to occur on a few
publicized sites and often takes place
from, on, or near roadways. Mountain
plover are relatively tolerant of
disturbance and often ignore humans in
vehicles. If approached on foot they
quickly retreat (Knopf and Wunder
2006). We believe that observation by
birders does not represent a threat to the
mountain plover because it is limited in
extent and most birders attempt to
minimize disturbance to birds as they
pursue their activities.
Most research conducted on mountain
plover relies on passive sampling (e.g.,
point counts) rather than active
handling. Passive sampling is not likely
to substantially affect the mountain
plover. The studies that involve
handling of adults, chicks, and eggs may
impact individuals, but these studies are
small enough in scale that they are not
likely to affect populations as a whole.
Knopf and Wunder (2006) cautioned
mountain plover eggs could become
overheated if exposed to direct sun on
hot days. However, we do not have any
information to indicate that this has
caused decreased nest success in areas
where research occurs.
Factor C. Disease or Predation
Summary of Factor B
We do not have any evidence of risks
to mountain plover from overutilization
for commercial, recreational, scientific,
or educational purposes, and we have
no reason to believe that that this factor
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Disease
We are not aware of any diseases or
parasites that pose a threat to the
mountain plover at this time. West Nile
virus, which has been documented to
cause deaths in many bird species, has
not been found in mountain plover
(Andres and Stone 2009, p. 29). Since
2007, 4,888 dead birds have been
identified throughout California as
deaths attributed to the West Nile virus
(California Department of Public Health
(CDPH) 2010). Within this time span,
West Nile virus has been reported from
a number of Central Valley counties, but
to date no mountain plover deaths have
been attributed to the virus (CDPH
2010). Over the same time period, there
have been no bird deaths associated
with West Nile virus in Imperial
County.
Dreitz et al. (2010) investigated causes
of mortality in mountain plover chicks
and reported preliminary analysis of
blood samples from chicks in Colorado
and Montana. Blood parasitism was low
in Colorado, and none was detected in
Montana.
The Intergovernmental Panel on
Climate Change (IPCC) (2007, p. 51)
suggests that the distribution of some
disease vectors may change as a result
of climate change. However, we have no
information to suggest any specific
disease may become problematic to the
mountain plover as a result of climate
change.
Predation
The list of predators on mountain
plover, their nests, and young is
extensive, and includes the American
badger (Taxidea taxus), skunks
(Spilogale spp. and Mephitis spp.),
ground squirrels, swift fox (Vulpes
velox), coyote (Canis latrans), bullsnake
(Pituophis catenifer), Swainson’s hawk
(Buteo swainsoni), prairie falcon (Falco
mexicanus), common raven (Corvus
corax), great-horned owl (Bubo
virginianus), burrowing owl (Athene
cunicularia), and loggerhead shrike
(Lanius ludovicianus) (Smith and
Keinath 2004, p. 20; Andres and Stone
2009, p. 28).
Survival rates of adult mountain
plover are thought to be quite high on
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both breeding and wintering grounds,
and it is unlikely that predation of adult
mountain plover constitutes a
significant concern to mountain plover
populations overall (Smith and Keinath
2006, p. 19). Emphasis has been largely
placed on predation of nests and chicks
(Kopf and Wunder 2006; Andres and
Stone 2009, p. 28; Dreitz et al. 2010,
entire). Survival of nests to hatching is
similar to or greater than that found in
other ground-nesting prairie shorebirds
in the Great Plains, and nest success
does not appear to be a limiting factor
to population growth of the species
(Dinsmore et al. 2010). Survival of
chicks from hatching to fledging has
been highlighted as a potentially
important life stage that could be
targeted for management to support the
conservation and expansion of
mountain plover populations, for
example, from habitat improvements
that may reduce predation rate
(Dinsmore et al. 2010).
Knopf (2008, p. 50) cited the swift fox
as the major predator on eggs and the
primary predator on chicks on the PNG
in Colorado, and suggested that reduced
predator control and subsequent
increase in predators was a contributing
factor in the dramatic decline in
mountain plover the area experienced.
Thirteen-lined ground squirrels
(Spermophilus tridecemlineatus) have
been the greatest source of nest
predation in South Park, Colorado
(Wunder 2010b, pers. comm.). Chick
monitoring in Colorado in 2010
confirmed 38 mortalities, including 13
from avian predation (most on less than
16-day old chicks by burrowing owls)
and 8 by mammalian predators
including swift fox and American
badger (Dreitz et al. 2010, pp. 3–4).
Predation by unknown species was
suspected in some other deaths (Dreitz
et al. 2010, pp. 3–4). Similar research in
Montana in 2010 implicated blackbilled magpies (Pica hudsonia) as a
possible cause of disappearances of
chicks whose fate was not confirmed.
Knopf and Wunder (2006) suggested
mountain plover nest visits by
researchers could lead to predation by
ravens (Corvus spp.). Similarly, nest
marking to avoid nest destruction
during agricultural operations may alert
predators to nest locations.
We do not believe that natural levels
of predation present a threat to the
mountain plover, although the risk
could be increased through human
development and habitat fragmentation.
This may result where predators
concentrate their foraging activities and
movements along habitat edges.
However, Mettenbrink et al. (2006, p.
195) looked at mountain plover nesting
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in a prairie landscape fragmented by
crop fields and found little relationship
between nest predation and distance to
habitat edges. The authors concluded
that predators of mountain plover in the
shortgrass prairie apparently do not
hunt selectively along anthropogenic
(human-created) edges. Roads may serve
as travel routes for predators (Pitman et
al. 2005, p. 1267), and natural gas
development has been shown to
increase the occupancy of the common
raven, a potential predator of mountain
plover nests and chicks, in sage brush
habitat (Bui et al. 2010, pp. 73–74).
Increases in roads and structures
associated with energy development
could result in increased predation on
mountain plover nests or chicks.
However, Carr (in review) found no
relationship between mountain plover
nest success and road or well density.
While predation accounts for a major
portion of chick mortality, we have no
information that would lead us to
conclude that predation on mountain
plover chicks differs from levels
experienced by other upland nesting
shorebirds or that, across the range of
the mountain plover, it is a current or
future threat to the survival of the
species.
Summary of Factor C
We do not find evidence that disease
is currently impacting the mountain
plover, nor do we have information to
indicate that disease outbreaks will
increase in the future. While the level of
predation on mountain plover nests and
chicks is high, it is not inconsistent with
that found in other ground-nesting bird
species. Fragmentation of habitats,
including that associated with energy
development, could increase predation,
but evidence to date does not suggest
any increase is occurring. We do not
have information at this time to indicate
that predation is impacting the
mountain plover at a level that threatens
the species. We conclude that the best
scientific and commercial information
available indicates that the mountain
plover 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.
Factor D. The Inadequacy of Existing
Regulatory Mechanisms
Under this factor, we examine
whether existing regulatory mechanisms
are inadequate to address the threats to
the mountain plover discussed in
Factors A, B, C and E. The Service
considers regulatory mechanisms to
mean all mechanisms that are related to
a comprehensive regime designed to
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maintain a conserved wildlife
population. In addition to the five
factors that section 4(a)(1) of the Act
directs the Service to consider, section
4(b)(1)(A) of the Act requires the Service
to take into account, ‘‘those efforts, if
any, being made by any State or foreign
nation, or any political subdivision of a
State or foreign nation, to protect such
species. * * *’’ We consider these
efforts when developing our threat
analyses under all five factors and in
particular under Factor D. Therefore,
under Factor D we consider not only
laws and regulations, but other
mechanisms that are part of a regulatory
process such as management plans and
agreements, conservation practices, and
so forth.
In analyzing whether the existing
regulatory mechanisms are inadequate,
the Service reviews relevant Federal,
State, and Tribal laws, plans,
regulations, Memoranda of
Understandings (MOUs), Cooperative
Agreements, and other such
mechanisms that influence
conservation. We give strongest weight
to statutes and their implementing
regulations, and management direction
that stems from those laws and
regulations. An example would be the
terms and conditions attached to a
grazing permit that describe how a
permittee will manage livestock on a
BLM allotment. They are nondiscretionary and enforceable, and are
considered a regulatory mechanism
under this analysis. Other examples
include State governmental actions
enforced under a State statute or
constitution, or Federal action under
statute. Some other agreements (MOUs
and others) are more voluntary in
nature; in those cases we analyze the
specific facts for that mechanism to
determine the extent to which it can be
relied on in the future. We consider all
pertinent information, including the
efforts and conservation practices of
State governments, whether or not these
are enforceable by law. Regulatory
mechanisms, if they exist, may preclude
the need for listing if such mechanisms
are judged to adequately address the
threat to the species such that listing is
not warranted.
Conversely, threats on the landscape
are not ameliorated when not addressed
by existing applicable regulatory
mechanisms, or when the existing
mechanisms are not adequate (or not
adequately implemented or enforced).
We cannot predict when or how State
and Federal laws, regulations, and
policies will change; however, most
Federal land use plans are valid for at
least 20 years. In this section, we review
actions undertaken by State and Federal
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entities designed to reduce or remove
threats to mountain plover and its
habitat.
Federal Laws and Regulations
The mountain plover is covered under
the provisions of the Migratory Bird
Treaty Act (MBTA), which provides
regulatory protection for mountain
plover by prohibiting actions causing
direct mortality and destruction of
nests. In addition, the mountain plover
is listed as a Bird of Conservation
Concern by the Service in all 12 Bird
Conservation Regions encompassing the
species’ breeding and wintering ranges.
Birds of Conservation Concern represent
the highest conservation priorities
under the MBTA for the Service’s
Migratory Bird Program (Service 2008,
p. iii). The goals of the Service’s
Migratory Bird Program include the
protection, restoration, and management
of migratory bird populations to ensure
long-term ecological sustainability
(Service 2011). The Service’s goal is to
prevent or remove the need for
additional bird listings under the Act by
implementing proactive management
and conservation actions. The list is to
be used to develop research, monitoring,
and conservation actions to stimulate
coordinated and collaborative proactive
conservation actions among Federal,
State, Tribal, and private partners
(Service 2008, p. iii). However, the
designation as a Bird of Conservation
Concern does not in and of itself
provide any extra protections for the
mountain plover or its habitat.
The BLM and the USFS are the
primary Federal agencies that manage
lands that provide breeding or wintering
habitat for the mountain plover. The
BLM’s lands and USFS-managed
National Grasslands provide important
breeding habitat in Montana, Wyoming,
Colorado, and New Mexico. The BLM’s
lands in California and southern
Arizona may provide habitat for
wintering mountain plover.
The Federal Land Policy and
Management Act of 1976 (FLPMA) (43
U.S.C. 1701 et seq.) is the primary
Federal law governing most land uses
on BLM-administered lands. Section
102(a)(8) of FLPMA (43 U.S.C.
1701(a)(8)) specifically recognizes
wildlife and fish resources as being
among the uses for which these lands
are to be managed. Regulations pursuant
to FLPMA and the Mineral Leasing Act
(30 U.S.C. 181 et seq.) that address
wildlife habitat protection on BLMadministered land include 43 CFR
3162.3–1 (Drilling applications and
plans) and 43 CFR 3162.5–1
(Environmental obligations); subpart
4120 (Grazing Management) of Title 43
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of the Code of Federal Regulations
(CFR); and subpart 4180 (Fundamentals
of Rangeland Health and Standards and
Guidelines for Grazing Administration)
of Title 43 of the CFR.
Mountain plover have been
designated as a BLM Sensitive Species
in Colorado (BLM 2000a), California
(BLM 2006), and Wyoming (BLM
2010a). The management guidance
afforded sensitive species under BLM
Manual 6840—Special Status Species
Management (BLM 2008, entire) states
that ‘‘Bureau sensitive species will be
managed consistent with species and
habitat management objectives in land
use and implementation plans to
promote their conservation and to
minimize the likelihood and need for
listing under the [Act]’’ (BLM 2008, p.
05V). The BLM Manual 6840 further
requires that Resource Management
Plans (RMPs) should address sensitive
species, and that implementation
‘‘should consider all site-specific
methods and procedures needed to
bring species and their habitats to the
condition under which management
under the Bureau sensitive species
policies would no longer be necessary’’
(BLM 2008, p. 2A1). See our discussion
above under Factor A, Energy and
Mineral Development, for more on
measures the BLM has taken in
Wyoming to conserve the mountain
plover as a sensitive species.
The BLM in Montana has designated
a Mountain Plover Area of Critical
Environmental Concern (ACEC), which
contains 24,730 ac (9,892 ha) of habitat
suitable for breeding mountain plover
(BLM 2000b, p.1). Management
prescriptions apply within the ACEC to
protect breeding mountain plover
during its nesting period. All
construction activity and surface
disturbance are prohibited from April 1
to July 31, road construction is
minimized within the ACEC, and
seasonal restrictions also apply to offhighway travel (BLM 2000b, pp. 8–9).
While the ACEC is a focus of BLM’s
efforts to conserve the mountain plover,
the area covers only a small fraction of
all mountain plover habitat in Montana.
As a designated sensitive species
under BLM Manual 6840, mountain
plover conservation must be addressed
in the development and implementation
of RMPs on BLM lands. RMPs are the
basis for all actions and authorizations
involving BLM-administered lands and
resources. They establish allowable
resource uses, resource condition goals
and objectives to be attained, program
constraints and general management
practices needed to attain the goals and
objectives, general implementation
sequences, and intervals and standards
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for monitoring and evaluating the plan
to determine effectiveness and the need
for amendment or revision (43 CFR
1601.0–5(n)). The RMPs provide a
framework and programmatic guidance
for activity plans, which are site-specific
plans written to implement decisions
made in an RMP. Examples include
Allotment Management Plans that
address livestock grazing, oil and gas
field development, travel management
(motorized and mechanized road and
trail use), and wildlife habitat
management. Activity plan decisions
normally require additional planning
and National Environmental Policy Act
(NEPA; 42 U.S.C. 4321 et seq.) analysis.
If an RMP contains specific direction
regarding mountain plover habitat,
conservation, or management, it
represents an enforceable regulatory
mechanism to ensure that the species
and its habitats are considered during
permitting and other decision-making
on BLM lands.
The BLM has regulatory authority for
oil and gas leasing on Federal lands and
on private lands with a severed Federal
mineral estate, as provided at subpart
3100 (Onshore Oil and Gas Leasing;
General) of Title 43 of the CFR, and they
are authorized to require stipulations as
a condition of issuing a lease. They can
condition ‘‘Application for Permit to
Drill’’ authorizations, conducted under a
lease that does not contain specific
mountain plover conservation
stipulations, but utilization of
conditions is discretionary, and we are
uncertain as to how this authority is
applied.
Management of National Forest
System lands is guided principally by
the National Forest Management Act
(NFMA) (16 U.S.C. 1600–1614, August
17, 1974, as amended). The NFMA
specifies that all National Forests must
have a Land and Resource Management
Plan (LRMP) (16 U.S.C. 1604) to guide
and set standards for all natural
resource management activities on each
National Forest or National Grassland.
The NFMA requires USFS to
incorporate standards and guidelines
into LRMPs (16 U.S.C. 1604(c)). The
USFS conducts NEPA analyses on its
LRMPs, which include provisions to
manage plant and animal communities
for diversity, based on the suitability
and capability of the specific land area
in order to meet overall multiple-use
objectives. The USFS planning process
is similar to that of the BLM. The
mountain plover is a USFS sensitive
species in Region 2, which includes all
of Colorado and portions of Wyoming
and Nebraska.
The USFS policy provides direction
to analyze potential impacts of proposed
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management activities to sensitive
species in a biological evaluation. The
LRMPs for grassland units within USFS
Region 2 (PNG, Nebraska National
Forest, and Thunder Basin National
Grassland in Wyoming) contain
management direction for the mountain
plover (USFS 2001). Some examples of
the LRMP standards (required measures)
for the three areas include: (1)
Prohibiting development of new
facilities within 0.25 mi (0.40 km) of
known mountain plover nests or nesting
areas; (2) limiting vehicle speeds in
occupied mountain plover habitat to 25
miles per hour (mph) (40 kilometers per
hour (kph)) on resource roads and 35
mph (56 kph) on local roads; (3)
designing vegetation management
projects in suitable mountain plover
habitat to maintain or improve
mountain plover habitat; and (4)
maintaining occupied nesting and
brooding habitat on black-tailed prairie
dog colonies by limiting new oil and gas
development to one well per 80 ac (32
ha) within occupied habitat.
Cumulatively, structure and facility
development will not occur on more
than 2 percent of the occupied
mountain plover nesting habitat in each
prairie dog colony on the Thunder Basin
National Grasslands (USFS 2001). As
described above in the discussion under
Factor A, the PNG has been conducting
prescribed burning for many years to
improve breeding habitat for mountain
plover (Knopf 2008, pp. 25–26).
Numerous research projects on
mountain plover have also been
conducted on the PNG and the adjacent
USDA Research Area (Augustine 2010a,
pers. comm.; Augustine 2010b, pers.
comm.).
In Colorado and Wyoming, a multiagency team, consisting of biologists
from the Service, BLM, USFS, and
National Park Service, developed a nonregulatory screening tool to allow for
proactive and consistent management
and conservation of the mountain
plover on public lands and to provide
a tool for streamlining agency review
and implementation of activities (BLM
2004). The screening tool allows agency
personnel to evaluate the impacts of
projects (such as energy development,
rangeland management, and recreation)
that would occur within or adjacent to
mountain plover habitat to determine
whether the project would result in an
impact to the species at the local or
rangewide scale. Use of the screening
tool would not stop any projects from
occurring, but rather would alert agency
personnel to possible project impacts so
that the project could be modified if
possible. While the screening tool
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provides a good non-regulatory
mechanism for Federal biologists in
Colorado and Wyoming to evaluate the
effects of their proposed actions, it does
not require that projects ultimately have
no effect on mountain plover. However,
this screening tool provides for
advanced notice of actions and
facilitates coordination between the
multi-state agency team.
The Federal laws, regulations, and
actions cited above are designed to
reduce or remove threats to the
mountain plover and its habitat. There
is no information available to indicate
that the species is threatened by the
inadequacy of existing Federal laws and
regulations.
State and International Laws and
Regulations
The Nebraska Game and Parks
Commission lists the mountain plover
as ‘‘threatened.’’ But, this regulatory
mechanism likely protects relatively few
individuals (see Conservation Status
and Local Populations above). While
some States, such as Colorado, have
specific management plans that address
mountain plover conservation, and all
States within the range of the species
include it within their State Wildlife
Conservation Strategies (see
Conservation Status and Local
Populations above), there is no
rangewide or intrastate coordinated
management effort and no requirement
to implement specific management
actions. However, there is no
information available to indicate that
the species is threatened by the
inadequacy of existing State regulatory
mechanisms.
Canada
The mountain plover has been listed
as endangered in Canada since 1987.
Knapton et al. (2006, p. i) noted that
listing was in part due to a perceived
decline from 1980 to 1986. The Species
At Risk Act (SARA), passed December
12, 2002, is a commitment by the
Canadian government to prevent the
extinction of wildlife and provide the
necessary actions for the recovery of
species deemed endangered. These atrisk wildlife species are provided with
legal protection under SARA, and their
biological diversity is thereby conserved
(Environment Canada 2010). As noted
in the Background section above, the
mountain plover population in Canada
is very small, and efforts there to
improve habitat will not likely have a
significant impact on this species’
conservation rangewide. There is no
information available to indicate that
the species is threatened by the
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inadequacy of existing regulatory
mechanisms in Canada.
Mexico
In 2001, Mexico established a list of
species classified as endangered,
threatened, under special protection, or
probably extinct in the wild
(Commission for Environmental
Cooperation (CEC) 2011). The mountain
plover was listed as threatened (Andres
and Stone 2009, p. 14). Under the
General Wildlife Law, the use of at-risk
species may be authorized only for the
collection and capture for restoration,
repopulation, and reintroduction
activities (CEC 2011). However,
regulatory powers and wildlife
management prerogatives reside largely
with the Federal government with States
taking a more minor role. Shifting
Federal agency responsibility and lack
of agency funding results in inadequate
protection and management of wildlife
resources (Valdez et al. 2006, p. 277).
Although regulatory mechanisms in
Mexico appear to be minimal or are not
adequately enforced, Mexico constitutes
a small portion of the overall species’
breeding range. Mountain plover appear
to winter in significant numbers in
Mexico, but at that time of year, they are
highly mobile and less vulnerable to
human activity than when nesting, and
they therefore may require few
regulatory protections. There is no
information available to indicate that
the species is threatened by the
inadequacy of existing regulatory
mechanisms in Mexico.
Summary
While mountain plover conservation
has been addressed in some State,
Federal, and international plans, laws,
regulations, and policies, none of these
have applicability throughout the range
of the mountain plover sufficient to
provide effective population-level
conservation. However, we have found
in the analysis of the other four factors
(A, B, C, and E) that there are no
activities that currently rise to the level
of a significant threat to the mountain
plover. Therefore, we conclude that the
best scientific and commercial
information available indicates that the
mountain plover is not now, and is not
expected to become within the
foreseeable future, threatened by the
inadequacy of existing 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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ranged from 0.74 to 0.96 yearly
Factor E. Other Natural or Manmade
Factors Affecting the Species’ Continued (Dinsmore 2008, p. 50). Based on this
study, a mountain plover returning to its
Existence
breeding ground would likely return
Genetic Diversity
multiple additional years. Dinsmore et
The loss of local populations may
al. (2010) characterized the mountain
impact a species because local
plover as typical of relatively long-lived
populations may possess unique genetic bird species, documented to live over 10
characteristics that are important to the
years, where repeated reproductive
species’ genetic diversity and its ability
attempts throughout life are less
to adapt to future environmental
important to population growth than
changes. However, for mountain plover, adult survival. On the basis of our
genetic studies using nuclear
review of the best available information,
microsatellites have concluded that
we now believe that a short average
mountain plover across sampled
lifespan and resulting limited
breeding locations in Colorado and
reproductive opportunities, as suggested
Montana comprise a single, relatively
in our 2002 proposal, do not constitute
homogenous gene pool (Oyler-McCance a threat to the mountain plover.
2005, p. 359; Oyler-McCance et al. 2008,
In our February 16, 1999 (64 FR
pp. 496–497). These results suggest that 7587), and December 5, 2002 (67 FR
there is sufficient gene flow among
72396), proposals to list the mountain
breeding areas to offset reported adult
plover as a threatened species, we
fidelity to breeding areas and genetic
considered the plover to have high
effects of small populations (genetic
fidelity to breeding sites. In patchy
drift, loss of genetic diversity) (Oylerhabitat, when nesting habitat is
McCance et al. 2005, p. 360; Oylerdestroyed or unavailable, it may be
McCance et al. 2008, pp. 496–497).
difficult for the mountain plover to find
While this seems unusual for a species
a new place to breed, thus resulting in
with relatively high reported site
the decline of populations. Dispersal
fidelity, it suggests pair formation in
ability may be important to the use of
mixed winter flocks from different
available habitat and conservation of the
breeding areas. Widespread mixing of
mountain plover given the patchiness of
mountain plover populations in winter
desirable breeding habitat. Altered or
has been documented (Wunder 2007, p. fragmented landscapes may force
118). From a genetic perspective, this
mountain plover to disperse greater
information suggests that no single
distances. For example, in Montana,
breeding population requires special
where the mountain plover is highly
conservation or protection (Oylerdependent on black-tailed prairie dog
McCance et al. 2005, p. 360). However,
colonies for breeding habitat, sylvatic
not all populations have received
plague outbreaks often make previously
genetic analysis, including potentially
used breeding habitat undesirable. As
non-migratory breeding populations in
discussed above, Skrade and Dinsmore
Mexico. We conclude that there is no
(2010, pp. 671–672) demonstrated the
known restriction of gene flow within
mountain plover’s ability to disperse at
the species, and that the loss of any
least locally to exploit favorable
given local population will not
breeding habitats nearby, and in at least
substantially impact the genetic
one instance, an adult mountain plover
diversity of the mountain plover or the
returned to breed at a site about 25 mi
species’ ability to adapt to future
(40 km) from a site where it was banded
stressors.
during the previous season. We
conclude that while the mountain
Longevity, Site Fidelity, and Sex Ratio
plover generally exhibits fidelity to
In our December 5, 2002, proposed
breeding sites, it is capable, at least
listing rule (67 FR 72396), we stated,
locally, of seeking out and exploiting
‘‘* * * that because the average lifespan new habitat through both juvenile
of a mountain plover is less than 2
dispersal and through adult birds
years, and breeding does not occur until returning to different breeding sites in
1 year of age, an individual mountain
subsequent years. On a local scale
plover will likely have only one
(several mi/km), loss or fragmentation of
breeding season to contribute to
breeding habitat is unlikely to have an
population recruitment.’’ Previous study inordinate effect on mountain plover
results underestimated adult survival
survival and reproduction (i.e., effects
and, more importantly, our proposed
are likely to be proportional to, but not
rule erroneously concluded that average in excess of the amount of habitat loss).
lifespan reflected typical adult survival.
Previously, concern arose as to
In the best available estimate of adult
whether a preponderance of male
mountain plover among those birds
mountain plover survival, the annual
survival rate of adult mountain plover of handled by researchers in California
both sexes in Phillips County, Montana, suggested a skewed sex ratio (more
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males than females) range wide and
whether this might adversely affect
reproductive potential. Knopf (2003,
pers. comm.) speculated that a slightly
unbalanced sex ratio in California might
result from slightly higher overall
mortality in females or from differential
wintering, with females wintering
further south, in Mexico. Rangewide sex
ratios for mountain plover are still
unknown (Knopf and Wunder 2006) and
we have no evidence that relative
number of males and females in
mountain plover populations represents
a threat to the species.
Exposure to Pesticides
Potential exposure of mountain plover
to pesticides and agrochemicals on
wintering areas in California, and
resulting impacts to mountain plover
health and reproduction, have been
cited as a potential threat (Knopf and
Wunder 2006). Exposure of mountain
plover to direct pesticide application is
likely minimized because most
pesticide application occurs on growing
crops, and less frequently on harvested
and fallow fields, or grazed pastures that
mountain plover frequent.
The organochlorine agricultural
pesticide DDT, and its byproduct DDE,
can cause thinning of eggshells and
decreased reproductive success in birds
(Longcore et al. 1971, pp. 486, 489).
DDT has not been in use in California
since the 1970s, and in many cases, DDE
levels that remain in the environment
will decrease slowly over several
decades (Thomas et al. 2008, pp. 55,
65). Organochloride levels in mountain
plover collected from three California
counties (Imperial, San Luis Obispo,
and Tulare) in 1991–1992 ranged from
1.0 to 10.0 parts per million (ppm) (dry
weight); although these levels are
considered high for an upland bird, no
subsequent issues with bird behavior or
eggshell thickness in mountain plover
were noted (Knopf and Wunder 2006).
Levels of DDE of 43 ppm (wet weight)
were found in eggs collected from
abandoned mountain plover nests in
Park County, Colorado, in 2001 (Knopf
and Wunder 2006). No effects on eggs,
chicks, or adult mountain plover were
established.
Historically, soils in the Imperial
Valley are known to be high in DDE
(California Department of Food and
Agriculture (CDFA) 1985, p. 27). Studies
have shown unchanging levels of the
chemical in the past decades; this
suggests a persistent, local source of the
chemical (Gervais and Catlin 2004, pp.
509–510). The Imperial Valley is the
suspected source for high DDE
concentrations and decreased
reproductive success in white-faced
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ibises (Plegadis chihi) (Yates et al. 2010,
p. 159). Levels of DDE in resident
burrowing owls are suspected to act as
a stressor, but reproductive effects have
not been documented (Gervais and
Anthony 2003, p. 1259).
Service biologists recently collected
and analyzed mountain plover eggs,
soils, and soil invertebrates from
breeding areas in Colorado, Wyoming,
and Montana, and soils and soil
invertebrates from wintering areas in the
Imperial Valley (Zeeman 2011, pers.
comm.). Chemical analyses of eggs
showed measurable, and in some cases
high, levels of persistent organic
pollutants, most notably DDE. Much
lower concentrations of polychlorinated
biphenyls (PPBs), hexachlorobenzene,
tetrachlorobenzenes, alpha chlordane,
oxychlordane (chlordane metabolite),
heptachlor epoxide, and dieldrin were
found. Contaminants detected in
mountain plover eggs were also detected
in soil and invertebrate samples from
fields in Imperial Valley, but no
measurable levels were found in soil
and invertebrates at the breeding
grounds.
The upper concentrations of DDE
detected, 50 ppm (wet weight) in two
eggs, was within the range of values
(which can range from as low as 3 ppm
in sensitive species to 30 ppm in less
sensitive species) associated with
eggshell thinning and reproductive
impairments in wild birds (Blus 1996).
Conspicuous signs of impacts associated
with DDE exposure, such as eggshell
cracking and embryo malformation,
were not detected in mountain plover
(Zeeman 2011, pers. comm.). Based on
concentrations found in eggs, DDE from
wintering areas, including the Imperial
Valley, could potentially affect
mountain plover (Zeeman 2011, pers.
comm.). The potential for the other
contaminants detected in eggs, both
individually or in combination, to affect
the mountain plover is being evaluated
by the Service (Zeeman 2011, pers.
comm.). The results cited above suggest
that exposure varies by individual and
that few mountain plover have DDE
levels that raise a concern. In addition,
no effects of DDE to adult mountain
plover, their eggs, or chicks have been
established. At this time, we believe that
if an effect occurs, it would probably be
localized, and would affect individual
birds or eggs and not have an effect at
a population or species level.
Certain organophosphate insecticides
are still used to control insect pests on
crops in California’s Central Valley
within the range of the mountain plover.
Iko et al. (2003, p. 119) measured
cholinesterase levels in mountain
plover, a measure of exposure to
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organophosphorus and carbamate
insecticides, and found that they varied
widely between mountain plover
collected in California from the Central
Valley where pesticide use is
widespread and from the Carrizo Plain
where there is minimal pesticide use,
but no differences were observed in
mountain plover body condition.
The Central Valley is one of the
State’s primary growing regions for
alfalfa. Sixty percent of the State’s hay
crop is grown here, with over 600,000
ac (240,000 ha) planted to alfalfa within
the Central Valley (Godfrey 2002, p. 4).
Insecticides used on alfalfa pests
include chlorpyrifos, malathion, and
pyrethroids. Insecticide applications in
alfalfa usually occur once insects reach
damaging levels, typically in March or
later in the growing season (Godfrey
2002, pp. 4–10), suggesting that
exposure of wintering mountain plover
to treatments would be limited, if any.
Because early spring insecticide
treatments in alfalfa have been found to
largely eliminate nontarget insect
species complexes (Godfrey 2002, pp.
4–6), an unknown but potential residual
effect to mountain plover prey
availability may exist in specific areas
the following winter. If present, such an
effect could locally reduce desirability
of certain alfalfa fields to wintering
mountain plover, but would not have a
rangewide impact to the species.
Malathion, a broad-spectrum
organophosphate insecticide, has been
used to control the beet leaf-hopper
(Circulifer tenellus) in rangeland habitat,
fallow fields, oil fields, and cultivated
areas on both public and private lands
in the San Joaquin Valley (BLM 2002,
pp. 1–2; CDFA 2007, p. 8; CDFA 2008,
pp. 1–4). The beet leaf-hopper is a
vector for curly top virus, which
negatively affects crops. In the western
and southern portions of the San
Joaquin Valley, aerial spraying may
occur fall through spring, and may
include treatment of approximately
200,000 ac (80,000 ha) in years with
high beet leaf-hopper populations.
Treatment usually results in a target
population decline of over 90 percent
(CDFA 2008, pp. 1–4). Potential impacts
to the mountain plover from the control
treatments could result from both direct
exposure and indirectly from the
reduction of insect prey (CDFA 2007, p.
79).
Although beet leaf-hopper control is
potentially immense in scale, in the 10
years up to 2002, an average of only
about 4,400 ac (1,800 ha) per year were
treated in the bird’s wintering range
within the San Joaquin Valley, primarily
in sloped terrain that is not thought to
be desired by the mountain plover
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(CDFA 2007, p. 79). The limited area
and quality of mountain plover habitat
treated, coupled with the species’ large
wintering range in California, led the
CDFA to determine that the curly top
treatment program would not be likely
to significantly impact the mountain
plover (CDFA 2007, p. 80). On public
lands managed by the BLM, prescribed
usage avoids malathion spraying on
wintering mountain plover areas when
the plover is present (BLM 2002, p. 1).
Chemical exposure in Mexico where
regulations and enforcement may be less
stringent could be of concern (Andres
and Stone 2009, p. 30). DDE levels in
mountain plover eggs reported by
Zeeman (2011, pers. comm.) may have
resulted from exposure in Mexico,
where DDT is still used. While we
believe that crop fields in Mexico have
potential to support large numbers of
wintering mountain plover, significant
mountain plover use of crop fields in
Mexico has not been reported (MaciasDuarte and Punjabi 2010, pp. 3, 7), nor
have specific issues regarding pesticide
use and impact to mountain plover been
identified. While changing agricultural
practices regarding pesticide application
or evolution of new chemicals for use in
the United States or Mexico could prove
a future threat, we have no basis for
predicting the potential of such an
occurrence.
We have no evidence that pesticides
are significantly impacting mountain
plover populations either locally or
rangewide. However, given the
information summarized above,
additional evaluation of any possible
effects to mountain plover from former
and ongoing pesticide use within the
mountain plover’s range appears
prudent.
Selenium Toxicity
Within the western San Joaquin
Valley, selenium is present in the soil
and has the potential to occur in ponded
irrigation water in fields and drainages.
Irrigation with drainwater used to flood
wetlands has resulted in biological
accumulation of selenium sufficient to
harm reproduction of shorebirds and
other wildlife (Ohlendorf et al. 1987,
pp. 169–171, 174–181). Potential effects
of selenium poisoning on birds can
include gross embryo deformities,
winter stress syndrome, depressed
resistance to disease due to depressed
immune system function, reduced
reproductive success, reduced juvenile
growth and survival rates, mass wasting,
loss of feathers (alopecia), embryo
death, altered enzyme function, and
mortality (Ohlendorf 1996, pp. 131–139;
O’Toole and Raisbeck 1998, pp. 361–
380). Species exposed to multiple
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stressors can become more vulnerable to
exposure to selenium.
Because the mountain plover is an
upland bird feeding primarily on
terrestrial insects, its habits may limit
its exposure to selenium. Still, selenium
bioaccumulation in the food chain
could create a contaminant hazard for
mountain plover feeding on insects in
alkaline flats, grazed pastures, and
plowed fields in this area. Specific
exposure of the mountain plover to
selenium, or any adverse effects of such
exposure have not been documented.
In summary, it has been documented
that mountain plover have been exposed
to various levels of potentially harmful
pesticides and chemical toxins in
various portions of its range. However,
we have no information to indicate that
the mountain plover is responding
negatively to this exposure or that it is
likely to respond negatively in the
future. Exposure levels that elicit
negative responses in other bird species
do not appear to elicit a similar negative
response in mountain plover. Therefore,
we do not believe that mountain plover
are threatened by exposure to pesticides
and chemical toxins.
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Grasshopper and Cricket Control
Efforts to control grasshoppers and
Mormon crickets, especially Federal
control programs on BLM lands, have
been cited as potentially detrimental to
breeding mountain plover.
Grasshoppers occur throughout the
breeding range of the mountain plover
and can reach population levels
considered to be a threat to agriculture.
The USDA’s Animal and Plant Health
Inspection Service (APHIS) conducts
rangeland grasshopper and Mormon
cricket control, including areas
occupied by breeding mountain plover.
Logically, a significant reduction in
these mountain plover foods could
affect mountain plover fecundity and
survival. However, efforts to control
grasshoppers and Mormon crickets on
Federal lands are generally limited to
suppressing populations in years and
areas where infestations occur, and do
not have the goal of eradication, but
rather the goal of reducing densities to
levels that limit economic impacts (BLM
2010b). Numbers of these insects
present after treatment may remain
greater than those present in a normal
year. The BLM currently is pursuing a
strategy of ‘‘reduced area and agent
treatments,’’ with the majority of
treatments through aerial spraying of a
pesticide (diflubenzuron, a chiton
inhibitor) with limited impacts to nontarget species (BLM 2010b). Broad
spectrum insecticides (carbaryl and in
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limited cases malathion) are used more
sparingly, and as a secondary treatment.
Control on private lands can be
undertaken by State or local government
agencies, or private landowners without
participation or oversight by APHIS.
Treatment on private lands likely varies
depending on resources available and
the economic implications of
infestations. Where treatment occurs, it
likely has the similar goal of reducing
insect densities to acceptable levels.
Grasshopper and cricket control can
have an impact on mountain plover
prey and could, in some years and at
some locations, adversely affect
mountain plover breeding. However,
since the scope and impact of these
control efforts appear minimal relative
to the mountain plover breeding range,
we conclude that grasshopper and
Morman cricket control does not
represent a significant threat to
rangewide mountain plover
populations.
Weather
Annual weather variation influences
mountain plover habitat and breeding
success. Inclement weather may hinder
egg laying (Knopf and Wunder 2006).
Cold, rain, and hail can result in loss of
nests and decreased chick survival.
Dreitz et al. (2010, pp. 3–4) identified
weather as a significant cause of chick
mortality. Mammalian predators of
mountain plover eggs and chicks are
scent-driven, and wet conditions
enhance predation (Knopf and Wunder
2006; Wunder 2007, p. 121).
Wunder (2007, pp. 119–121)
presented evidence that recruitment
may be linked to regional patterns of
weather, with highest recruitment
coming from breeding areas with low
precipitation and a subsequent 1- to 2year lag observed in increased
populations of adults (Wunder 2007, pp.
119–121). Productivity may be
influenced by drought cycles, with dry
years reducing predation from mammals
and suppressing vegetative growth, thus
providing increased accessibility to
insects. Annual survival of mountain
plover in Montana proved higher during
periods of drought, although prolonged
drought eventually decreases abundance
of insect foods (Dinsmore 2008, p. 52).
Weather variation affects mountain
plover productivity across its breeding
range, but we have no evidence that
normal weather fluctuations represent a
threat to the mountain plover.
Climate Change
There is no information available on
the direct relationship between the
environmental changes associated with
climate change and mountain plover
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27795
population trends. However, climate
change could potentially impact the
species. According to the IPCC (2007, p.
6), ‘‘warming of the climate system is
unequivocal, as is now evident from
observations of increases in global
average air and ocean temperatures,
widespread melting of snow and ice,
and rising global average sea level.’’
Average Northern Hemisphere
temperatures during the second half of
the 20th century were very likely higher
than during any other 50-year period in
the last 500 years and likely the highest
in at least the past 1,300 years (IPCC
2007, p. 30). It is very likely that over
the past 50 years cold days, cold nights,
and frosts have become less frequent
over most land areas, and hot days and
hot nights have become more frequent
(IPCC 2007, p. 6). It is likely that heat
waves have become more frequent over
most land areas, and the frequency of
heavy precipitation events has increased
over most areas (IPCC 2007, p. 30).
Changes in the global climate system
during the 21st century are likely to be
larger than those observed during the
20th century (IPCC 2007, p. 19). For the
next 2 decades, a warming of about 0.2
degrees Celsius (°C) (0.4 degrees
Fahrenheit (°F)) per decade is projected
(IPCC 2007, p. 19). Afterward,
temperature projections increasingly
depend on specific emission scenarios
(IPCC 2007, p. 19). Various emissions
scenarios suggest that by the end of the
21st century, average global
temperatures are expected to increase
0.6 to 4.0 °C (1.1 to 7.2 °F), with the
greatest warming expected over land
and at most high northern latitudes
(IPCC 2007, p. 46).
The IPCC (2007, p. 48) predicts that
the resiliency of many ecosystems is
likely to be exceeded this century by an
unprecedented combination of climate
change associated disturbances (e.g.,
flooding, drought, wildfire, and insects),
and other global drivers. Current climate
change predictions for terrestrial areas
in the Northern Hemisphere indicate
intense precipitation events, warmer air
temperatures, and increased summer
continental winds (Field et al. 1999, pp.
5–10; Cayan et al. 2005, pp. 6–28). With
medium confidence, IPCC predicts that
approximately 20 to 30 percent of plant
and animal species assessed so far are
likely to be at an increased risk of
extinction if increases in global average
temperature exceed 1.5 to 2.5 °C (3 to
5 °F).
The mountain plover is primarily a
species of grasslands and semi-desert.
Grasslands in the Great Plains of the
United States and southern Canada are
predicted to get warmer and drier with
climate change (North American Bird
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Conservation Initiative 2010, p.18).
Southwestern grasslands are expected to
become drier because of declining
precipitation and higher temperatures,
especially the Chihuahuan Desert
grasslands of the southwestern United
States and northern Mexico, which are
critical wintering areas for many
grassland birds, including the mountain
plover (North American Bird
Conservation Initiative 2010, p.18). In
northern grasslands, additional
precipitation is expected, but they will
still become drier because warmer
temperatures will cause increased
evaporation (North American Bird
Conservation Initiative 2010, p. 18).
Variability in precipitation is also
expected to increase; droughts, flooding,
and extreme storms (such as hailstorms)
are all expected to become more
common (North American Bird
Conservation Initiative 2010, p.18).
Increased atmospheric carbon dioxide
will probably contribute to invasions of
woody shrubs into grasslands (North
American Bird Conservation Initiative
2010, p. 18), which could make certain
habitats unusable for the mountain
plover.
Climate Wizard (TNC 2007) predicts
an average temperature increase of
approximately 4 to 6 °F by the 2050s for
the majority of mountain plover
breeding and wintering habitat within
the United States. Precipitation is
projected to decline slightly in the
southwest portion of the range, and to
increase by 10 to 15 percent in the more
northern portions of the range in the
same time period. However, as stated
above, warmer temperatures and
evaporation may offset any gains in
precipitation. By the 2080s,
temperatures are predicted to increase
by as much as 7.5 °F within the species’
breeding range, and precipitation to
decline from 2050s levels throughout
the range (TNC 2007). Weather data in
the Imperial Valley recorded by the
Desert Research Institute of the Western
Regional Climate Center (WRCC)
between 1927 and 2010 show an
increasing trend in average temperature
during the months of September
through March, when mountain plover
are present in the area (WRCC 2010a,
Figure 1). Projected temperature change
for the Imperial Valley was obtained
through the Climate Wizard, in which
an average of all models was used to
display change in temperature. These
data indicate a 3.9 °F increase in
temperature for the 2050s and a 5.7 °F
increase for the 2080s (TNC 2007). The
WRCC also documented in Imperial,
California, a slight increasing trend in
average precipitation (inches) from
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1925–2010 (WRCC 2010b). Projected
change in precipitation values for the
Imperial Valley was also obtained
through the Climate Wizard in which an
average of all models was used to
display percent change in precipitation.
These data indicate a 1.1 percent
increase in precipitation for the 2050s
and an increase of 0.3 percent by the
2080s (TNC 2007).
Change in plant phenology (timing of
life cycle events such as vegetative
growth and reproduction) may be one of
the earliest observed responses to rapid
global climate change and could
potentially have serious consequences
both for plants and animals that depend
on periodically available resources
(Moza and Batnegar 2005, p. 243). A
change in the timing of availability of
insects that mountain plover and their
chicks rely on as a food source could
occur as a result in changes in plant
phenology.
Because they are often highly
competitive, invasive plant species are
altering the plant composition of
ecosystems and changing their structure
and function over large landscape areas.
Addition of fine fuels from these species
often increases fire frequency, which
can lead to increased dominance by
invasive species and further habitat
degradation. Climate change is
exacerbating these changes by altering
the amount and seasonal distribution of
precipitation and seasonal temperature
patterns in ways that often favor the
invasive species (Tausch 2008). This
could potentially result in changes in
the amount of ground cover in mountain
plover habitat, which could discourage
mountain plover nesting. Nonnative
wildlife species that could compete
with the mountain plover for resources
or prey on the species could potentially
move into their habitats.
Although the mountain plover was
not included in ‘‘The State of the
Birds—2010 Report on Climate Change’’
(North American Bird Conservation
Initiative), it was assessed using the
sensitivity traits analysis used in that
report (Sauer 2010b, pers. comm.). The
threat of climate change impacts to the
plover was considered low, as it was
only considered sensitive to one of the
five main traits (it was considered a
breeding obligate to a single habitat
type) (Sauer 2010b, pers. comm.).
Species that occupy only a single
habitat for breeding are vulnerable
should climate change reduce or
eliminate that habitat. While the
mountain plover has been often
described as a grassland obligate (i.e., is
dependent on grasslands for breeding),
it also breeds in agricultural fields, and
in semi-desert habitat. As such, we
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believe it is less likely to be threatened
by climate change impacting grassland,
or any one of its favored breeding
habitats, than is suggested by its
classification as a breeding obligate to a
single habitat type. The mountain
plover was not considered sensitive to
potential climate change impacts based
on the other four traits (its migratory
habits, dispersal ability, niche
specificity, and reproductive potential)
(Sauer 2010b, pers. comm.). In general,
the mountain plover seems to possess
characteristics that would allow it to
adapt to changing environmental and
climate conditions. See the North
American Bird Conservation Initiative
(2010, p. 28) for definitions of these
traits.
Specific information on mountain
plover suggests that the species might be
adapted to drought, and that climate
change predictions of the Great Plains
becoming warmer and drier might
benefit the species (Dinsmore 2008, p.
52). Andres and Stone (2009, p. 31)
predicted increased summer
temperatures and decreased
precipitation could benefit mountain
plover breeding. Recruitment of juvenile
mountain plover into the population
appears linked to regional patterns of
precipitation, with highest recruitment
coming from areas with lowest
precipitation every year, and a
subsequent increase in populations of
adults observed from the same areas
after a 1- to 2-year lag (Wunder 2007,
pp. 119–121). Annual survival of
mountain plover in Montana proved
higher during periods of drought,
despite potential reduction in insect
foods (Dinsmore 2008, p. 52). Peterson
(2003, pp. 291–292) concluded that
there have been subtle shifts northward
in ranges of grassland birds, including
mountain plover, potentially due to
climate change.
Climate change predictions are based
on models with assumptions, and there
are uncertainties regarding the
magnitude of associated climate change
parameters, such as the amount and
timing of precipitation and seasonal
temperature changes. There is also
uncertainty as to the magnitude of
effects of predicted climate parameters.
The mountain plover, along with its
habitat, will likely be affected in some
manner by climate change. A shift in the
species’ geographic range may occur
due to an increase in temperature and
drought, although climate change would
likely not pose as great a risk to
mountain plover habitat as it may to
species in polar, coastal, or montane
ecosystems. Nonnative and invasive
species, both plants and animals, could
move into plover habitat as a result of
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changes in temperature or precipitation
patterns and degrade nesting habitat or
compete with the mountain plover for
resources. A change in the timing of
availability of insects that mountain
plover and their chicks rely on as a food
source could occur as a result of
changes in plant phenology. There is no
information available to suggest that any
of these factors are impacting mountain
plover now or that they will likely
impact the species in the foreseeable
future.
Based on all the potential climate
change factors, a shift in range of the
species could be possible, but there is
no information available to suggest that
a net loss in occupied breeding habitat
or a significant impact to the status of
the species will result. Although
currently difficult to quantify, changes
in climate, including higher
temperatures, increasing stochastic
precipitation events, high winds, and
increasing soil dryness, will likely lead
to a loss of agricultural production in
the Imperial Valley; however, wintering
habitat seems adequate to support the
species. The species is adaptable to a
wide array of climes, as evidenced by a
geographic range that includes 12
States, Canada, and Mexico. Based on
the best available information on
climate change projections modeled
over the next 40 to 70 years, we do not
consider climate change to be a
significant threat to the mountain plover
at this time.
Human Disturbance
Knopf and Wunder (2006) stated that
mountain plover on nests are extremely
tolerant of human disturbance from
vehicles, tractors, and aircraft, but
quickly moved away when approached
by a human on foot. While adult
mountain plover would not likely be
affected by humans on foot, eggs left
unprotected for a period of time could
become overheated if exposed to direct
sun on hot days.
It seems likely that heavy
construction activities nearby could
impact nesting mountain plover. Such
activities are limited in scope across
mountain plover breeding habitat at any
one time. In addition, timing
stipulations that restrict construction
related to oil and gas development,
wind-power development, and some
other activities in the vicinity of
mountain plover during the nesting
season exist for some Federal lands
(Knopf and Wunder 2006).
Mountain plover are only one of a
number of breeding bird species found
in the habitats and locations where they
nest. While prohibitions under the
MBTA govern direct mortality and the
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destruction of mountain plover nests,
general awareness of MBTA protections
and of efforts to protect nesting birds,
their nests, and their eggs may help
limit human disturbance to nesting
mountain plover.
Andres and Stone (2009, p. 27)
suggested population-level effects from
human disturbance were unlikely. We
conclude that while human-caused
disturbance may impact mountain
plover, such impacts are generally of
limited scope, and human disturbance
is not likely a significant threat to the
species.
Cumulative Impacts
Some of the threats discussed in this
finding could work in concert with one
another to cumulatively create
situations that potentially impact the
mountain plover beyond the scope of
each individual threat. For example, as
discussed under Factor C, habitat
fragmentation, including energy
development that both alters habitat and
provides structure on which predators
could perch, could lead to increase in
predation on the mountain plover. We
have no data to determine if, or to what
extent, such a scenario is likely to occur.
We conclude, at this time, that it does
not present a threat to the future
existence of the mountain plover.
Similarly, under Factor A, we alluded
to the potential that in the Imperial
Valley and other areas of California,
human development, solar
development, changing agricultural
practices, water availability, and climate
change could interact to heighten
potential loss of mountain plover
wintering habitat. In the future,
warming climate may necessitate use of
more irrigation water for crops at the
same time that water availability
decreases due to expansion of human
population and related water demand.
In our best judgment, agriculture in the
Imperial Valley, and in other areas of
California that support the mountain
plover, are likely to be affected by some
variation of the above scenario.
However, specific changes in agriculture
are uncertain. Seasonal change in timing
of crops, potential change toward those
crops needing less water, and changes
in irrigation practices may or may not
detract from available wintering habitat
for mountain plover. While
cumulatively, these factors will likely
reduce the total area of wintering habitat
available, we believe that sufficient area
of appropriate agricultural habitat will
persist to support wintering mountain
plover.
We have not identified other likely
scenarios where the potential threats
discussed in the five factors above have
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potential to work in concert to
synergistically produce threats to the
mountain plover above those which we
have analyzed. We conclude that, at this
time, there are no identifiable
cumulative impacts likely to threaten
the existence of the mountain plover in
the foreseeable future.
Summary of Factor E
We conclude that the best scientific
and commercial information available
indicates that the mountain plover is
not now, or likely in the future,
threatened by genetic stochasticity, its
typical lifespan, its site fidelity,
exposure to pesticides, selenium
toxicity, grasshopper and cricket
control, weather, climate change, or
human disturbance, or cumulative
impacts of potential threats such that
the species is in danger of extinction or
likely to become so within the
foreseeable future.
Finding
As required by the Act, we considered
the five factors in assessing whether the
mountain plover is endangered or
threatened throughout all, or a
significant portion of its range. We have
carefully examined the best scientific
and commercial information available
regarding the status and past and
present and future threats faced by the
mountain plover. We reviewed
information in our files, other available
published and unpublished
information, and information provided
by interested parties following our
February 16, 1999, and December 5,
2002, proposals to list the mountain
plover (64 FR 7587 and 67 FR 72396,
respectively), and following our June 29,
2010, document (75 FR 37353) vacating
our September 9, 2003, withdrawal (68
FR 53083) and reinstating our 2002
proposal. We also consulted with
Federal and State land managers.
There have been historical impacts to
the mountain plover, in particular the
loss of much of the native prairie
ecosystem, including bison, prairie dog
colonies, other native grazers, and
wildfires that produced extensive
mountain plover habitat on the Great
Plains. However, past concerns
regarding continuing and future loss of
breeding habitat provided by blacktailed prairie dog colonies appears
unfounded. Conversion to agriculture
remains insignificant across the
mountain plover’s breeding range.
Human development and resultant
impact to mountain plover breeding
habitat in South Park, Colorado, has not
occurred as previously anticipated, and
is not expected to do so in the
foreseeable future. Little evidence has
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surfaced to suggest that the mountain
plover’s substantial use of cultivated
lands for breeding is problematic. The
potential for future energy development
to adversely affect mountain plover and
their habitat on their breeding or
wintering ranges is not fully known and
requires continued research. However,
studies to date do not lead us to
conclude that these activities currently
pose substantial threats to the mountain
plover or will in the foreseeable future.
Climate change may impact the
mountain plover, positively or
negatively, in ways not yet envisioned.
In the past, we were concerned that
mountain plover life span was short
compared to other plovers and that this,
in combination with high breeding site
fidelity, presented a threat to breeding
populations. Contrary to our previous
belief, the mountain plover is now
considered a relatively long-lived
species. Site fidelity and ability to seek
out alternative sites for breeding does
not appear to be a concern. Based on
new information regarding life span, site
fidelity, and dispersal, we no longer
believe that these aspects of the
mountain plover’s life history represent
any threat to the species. Lastly, recent
information confirms that some
mountain plover are exposed to
pesticides, but no evidence of impacts
to individuals, local populations, or
rangewide impacts to the species have
been demonstrated.
The current status of the mountain
plover does not suggest that future
habitat changes, or the combination of
climate change and habitat changes will
result in significant population-level
impacts in the foreseeable future. Their
geographically widespread breeding and
wintering locations, and ability to use a
variety of habitats, contribute to their
security. During breeding, they utilize
short- and mixed-grass prairie, prairie
dog colonies, agricultural lands, and
semi-desert (Dinsmore 2003, pp. 14–17).
The variety of habitats in which they
successfully breed suggests that threats
affecting one habitat type would not
greatly increase the mountain plover’s
vulnerability to extinction. Mountain
plover have proven to be adaptable to
many human activities, such as using
crop fields for breeding and wintering,
and benefitting from some cattle grazing
practices. Over time, the extent of
wintering habitat in California is likely
to decline, but wintering mountain
plover exploit a variety of grassland,
rangeland, crop fields, and semi-desert
landscapes from the Gulf Coast to the
Pacific Ocean. We conclude that any
foreseeable future declines in wintering
habitat, in California or elsewhere, are
unlikely to imperil the mountain plover.
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We estimate the current rangewide
mountain plover breeding population to
be over 20,000 birds. This is more than
double the estimate of 8,000 to 10,000
mountain plover that we cited in our
December 5, 2002, proposal to list the
mountain plover as a threatened species
(67 FR 72396). While we have no
evidence that an actual population
increase has occurred, a larger known
population provides added security
from current and future potential
influences and threats.
Based on our review of the best
available scientific and commercial
information pertaining to the five
factors, we find that the threats, alone or
cumulatively, are not of sufficient
imminence, severity, or magnitude to
indicate that the mountain plover is in
danger of extinction, or likely to become
endangered within the foreseeable
future, throughout all or a significant
portion of it range. The mountain plover
has experienced historical losses of
native habitat resulting in a significant
decline in the rangewide population.
However, BBS survey results suggest
that the recent (1999 through 2009) rate
of decline has moderated (see
Population Size and Trends above). We
have no evidence that potential threats
(as discussed in Factors A, B, C, D, and
E) are acting on the species or its habitat
in a way that would reverse this positive
trend or result in an increased rate of
population decline within the
foreseeable future. The currently
estimated rangewide mountain plover
population, more than 20,000 breeding
birds, is more than double that
estimated in 2002, providing the species
with added security should increased
threats to its wellbeing arise. As stated
above, the mountain plover’s
geographically widespread breeding and
wintering ranges, and ability to exploit
a variety of habitats, contribute to its
security. According to the Act, the term
‘‘endangered species’’ means any species
which is in danger of extinction
throughout all or a significant portion of
its range; the term ‘‘threatened species’’
means any species which is likely to
become an endangered species within
the foreseeable future throughout all or
a significant portion of its range. We
conclude that the mountain plover does
not meet the definition of endangered,
because there is an apparent trend
toward stability of the species’
rangewide population, it remains
widespread over both its breeding and
wintering ranges, and it can exploit a
variety of habitats including areas of
human disturbance. In addition, we
have found no threats acting on the
mountain plover in a way that would
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drive the species towards being
endangered in the foreseeable future;
therefore, the species does not meet the
definition of threatened. Therefore, we
find that listing the mountain plover as
an endangered or threatened species is
not warranted throughout all or a
significant portion of its range at this
time (see the Significant Portion of the
Range discussion below). As such, we
withdraw our December 5, 2002,
proposed rule (67 FR 72396) to list the
mountain plover as a threatened
species.
Distinct Vertebrate Population
Segments/Significant Portion of the
Range
After assessing whether the species is
endangered or threatened throughout its
range, we next consider whether a
distinct vertebrate population segment
(DPS) or whether any significant portion
of the mountain plover range meets the
definition of endangered or is likely to
become endangered in the foreseeable
future (threatened).
Distinct Vertebrate Population Segment
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 species
to which it belongs;
(2) The significance of the population
segment to the species to which it
belongs; and
(3) The population segment’s
conservation status in relation to the
Act’s standards for listing, delisting, 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
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status, or regulatory mechanisms exist
that are significant in light of section
4(a)(1)(D) of the Act.
We do not consider any population
segment of mountain plover to be
markedly separated from other
populations of the same taxon as a
consequence of physical, physiological,
ecological, or behavioral factors.
Mountain plover are naturally
distributed across a large landscape in a
discontinuous fashion. Available
breeding and wintering habitats exist in
a constantly shifting mosaic of suitable
habitat throughout the western Great
Plains and Rocky Mountain States from
Canada to Mexico. As an avian species,
mountain plover are able to move long
distances during migration, and to
return to different geographical areas for
breeding or wintering.
Although there is some evidence that
mountain plover exhibit some site
fidelity to their breeding areas (Graul
1973, p. 71; Skrade and Dinsmore 2010,
p. 672), other studies have shown that
the species can disperse over relatively
long distances (Knopf and Wunder
2006; Bly 2010b, pers. comm.). There
are no known barriers to movement
throughout the geographic range of the
species. Wunder (2007, p. 118)
concluded that there is widespread
mixing of mountain plover populations
in winter and that birds may use
alternate wintering sites in different
years. A genetic study using nuclear
microsatellites concluded that mountain
plover across sampled breeding
locations in Colorado and Montana
comprised a single, relatively
homogenous gene pool (Oyler-McCance
et al. 2008, pp. 496–497). Results
suggested that there was sufficient gene
flow among breeding areas to offset
genetic effects of small populations and
reported adult fidelity to breeding areas
(Oyler-McCance et al. 2008, pp. 496–
497).
The mountain plover spans
international boundaries between the
United States, Canada, and Mexico;
however, the vast majority of occupied
breeding habitat occurs in the United
States with few breeding records in
Canada and Mexico. Mexico likely
winters a substantial number of
mountain plover that breed in the
United States. The known relative
distribution of mountain plover between
the three countries has remained fairly
constant in recent years. Additionally,
we are not aware of any differences in
control of exploitation, management of
habitat, conservation status, or
regulatory mechanisms that exist in
Canada or Mexico that are significant in
light of section 4(a)(1)(D) of the Act (the
inadequacy of existing regulatory
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mechanisms). Therefore, we do not
believe that international boundaries
provide evidence of discrete mountain
plover populations.
We determine, based on a review of
the best available information, that no
mountain plover population segments
meet the discreteness conditions of the
1996 DPS policy. Therefore, no
mountain plover population segment
qualifies as a DPS under our policy, and
no DPS is 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. Because we found that no
mountain plover populations meet the
discreteness element and, therefore, do
not qualify as a DPS under the Service’s
DPS policy, we will not conduct an
evaluation of significance.
Significant Portion of the Range
The Act defines an endangered
species as one ‘‘in danger of extinction
throughout all or a significant portion of
its range,’’ and a threatened species as
one ‘‘likely to become an endangered
species within the foreseeable future
throughout all or a significant portion of
its range.’’ The term ‘‘significant portion
of its range’’ is not defined by the
statute. For the purposes of this finding,
a significant portion of a species’ range
is an area that is important to the
conservation of the species because it
contributes meaningfully to the
representation, resiliency, or
redundancy of the species. The
contribution must be at a level such that
its loss would result in a significant
decrease in the viability of the species.
If an analysis of whether a species is
endangered or threatened in a
significant portion of its range is
appropriate, we engage in a systematic
process that begins with identifying any
portions of the range of the species that
warrant further consideration. The range
of a species can theoretically be divided
into portions in an infinite number of
ways. However, there is no purpose in
analyzing portions of the range that are
not reasonably likely to be significant
and endangered or threatened. To
identify only those portions that warrant
further consideration, we determine
whether there is substantial information
indicating that (i) the portions may be
significant and (ii) the species may be in
danger of extinction there or likely to
become so within the foreseeable future.
In practice, a key part of this analysis is
whether the threats are geographically
concentrated in some way. If the threats
to the species are essentially uniform
throughout its range, no portion is likely
to warrant further consideration.
Moreover, if any concentration of
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27799
threats applies only to portions of the
range that are unimportant to the
viability of the species, such portions
will not warrant further consideration.
We next address whether any portions
of the mountain plover’s range warrant
further consideration. On the basis of
our review, we found no geographic
concentration of threats on breeding or
wintering habitat such that the
subspecies may be in danger of
extinction in that portion. Although the
mountain plover’s wintering habitat in
California is likely to decrease in the
future because of changes in land use
and agriculture, we have determined
that the likely extent of change will not
result in a significant threat to the
species’ ability to maintain a wintering
population in California. Similarly, we
found that there is no area within the
breeding range of the mountain plover
where the potential threat of changes to
habitat are concentrated or may be
substantially greater than in other
portions of the range. The factors
affecting the species are essentially
uniform throughout its range, indicating
that no portion of the mountain plover’s
range warrants further consideration of
possible endangered or threatened
status.
We request that you submit any new
information concerning the status of, or
threats to, the mountain plover to our
Colorado Ecological Services Office (see
ADDRESSES) whenever it becomes
available. New information will help us
monitor the mountain plover and
encourage its conservation. If an
emergency situation develops for the
mountain plover 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 Colorado Ecological Services
Office (see ADDRESSES).
Authors
The primary authors of this document
are the staff members of the Colorado
Ecological Services Office (see
ADDRESSES).
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: April 29, 2011.
Rowan W. Gould,
Acting Director, Fish and Wildlife Service.
[FR Doc. 2011–11056 Filed 5–11–11; 8:45 am]
BILLING CODE 4310–55–P
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[Federal Register Volume 76, Number 92 (Thursday, May 12, 2011)]
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[FR Doc No: 2011-11056]
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Vol. 76
Thursday,
No. 92
May 12, 2011
Part II
Department of the Interior
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Fish and Wildlife Service
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50 CFR Part 17
Endangered and Threatened Wildlife and Plants; Withdrawal of the
Proposed Rule To List the Mountain Plover as Threatened; Proposed Rule
Federal Register / Vol. 76 , No. 92 / Thursday, May 12, 2011 /
Proposed Rules
[[Page 27756]]
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DEPARTMENT OF THE INTERIOR
Fish and Wildlife Service
50 CFR Part 17
[Docket No. FWS-R6-ES-2010-0038; MO 92210-0-0008-B2]
RIN 1018-AX26
Endangered and Threatened Wildlife and Plants; Withdrawal of the
Proposed Rule To List the Mountain Plover as Threatened
AGENCY: Fish and Wildlife Service, Interior.
ACTION: Proposed rule; withdrawal.
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SUMMARY: We, the U.S. Fish and Wildlife Service (Service), announce our
decision to withdraw the proposed listing of the mountain plover
(Charadrius montanus) as a threatened species under the authority of
the Endangered Species Act of 1973, as amended (Act). After a thorough
review of all available scientific and commercial information, we have
determined that the species is not endangered or threatened throughout
all or a significant portion of its range. We make this determination
because threats to the species as identified in the proposed rule are
not as significant as earlier believed and currently available data do
not indicate that the threats to the species and its habitat, as
analyzed under the five listing factors described in section 4(a)(1) of
the Act, are likely to endanger the species in the foreseeable future
throughout all or a significant portion of its range.
DATES: The December 5, 2002 (67 FR 72396), proposal to list the
mountain plover as a threatened species is withdrawn as of May 12,
2011.
ADDRESSES: This finding is available for viewing on the Internet at
https://www.regulations.gov (see Docket No. FWS-R6-ES-2010-0038) and
https://www.fws.gov/mountain-prairie/species/birds/mountainplover and
also by appointment, during normal business hours, at the U.S. Fish and
Wildlife Service, Colorado Ecological Services Office, 134 Union
Boulevard, Suite 670, Lakewood, CO 80225; telephone 303-236-4773;
facsimile 303-236-4005. Please submit any new information, materials,
comments or questions concerning this finding to the Colorado
Ecological Services Field Office at P.O. Box 25486, DFC (MS 65412),
Denver, Colorado 80225.
FOR FURTHER INFORMATION CONTACT: Susan Linner, Field Supervisor, U.S.
Fish and Wildlife Service, Colorado Ecological Services Field Office
(see ADDRESSES). If you use a telecommunications device for the deaf
(TDD), call the Federal Information Relay Service (FIRS) at 800-877-
8339.
SUPPLEMENTARY INFORMATION:
Background
Previous Federal Actions
For a detailed description of Federal actions concerning the
mountain plover, please refer to the February 16, 1999, proposed rule
to list the species (64 FR 7587); the December 5, 2002, proposed rule
to list the species with a special rule under section 4(d) of the Act
(16 U.S.C. 1531 et seq.) (67 FR 72396); and the September 9, 2003,
withdrawal of the proposed rule to list the species (68 FR 53083).
The document we published on September 9, 2003 (68 FR 53083),
withdrew the entire proposed rule we published on December 5, 2002 (67
FR 72396), including our proposal to list the mountain plover as a
threatened species and our proposed special 4(d) rule. The September 9,
2003, document also addressed comments we received on both the 1999 and
2002 proposals to list the mountain plover and summarized threat
factors affecting the species. The withdrawal of the proposed rule was
based on our conclusion that the threats to the mountain plover
identified in the proposed rule were not as significant as previously
believed and that currently available data did not indicate that
threats to the species and its habitat, as analyzed under the five
listing factors described in section 4(a)(1) of the Act, were likely to
endanger the species in the foreseeable future throughout all or a
significant portion of its range.
On November 16, 2006, Forest Guardians (now WildEarth Guardians)
and the Biological Conservation Alliance filed a complaint in the
District Court for the Southern District of California challenging the
September 9, 2003, withdrawal of the proposal to list the mountain
plover (68 FR 53083). We entered into a settlement agreement with the
plaintiffs, which was filed by the court on August 28, 2009. As part of
the settlement agreement, we agreed to reconsider our decision to
withdraw the proposed listing of the mountain plover and to submit to
the Federal Register by July 31, 2010, a document reopening the
December 5, 2002, proposal to list the mountain plover (67 FR 72396)
that would also request public comments. We agreed to vacate our 2003
withdrawal of the proposed rule upon publication of the Federal
Register notice reopening public comment on the December 5, 2002,
proposal to list the mountain plover (67 FR 72396). We further agreed
to submit a final listing determination for the mountain plover to the
Federal Register no later than May 1, 2011.
On June 29, 2010, we published a document in the Federal Register
notifying the public that we were reinstating that portion of our
December 5, 2002, proposed rule to list the mountain plover as
threatened under the Act (75 FR 37353). We did not reinstate that
portion of the December 5, 2002, proposed rule regarding a proposed
special rule under section 4(d) of the Act. The proposed special rule
was designed to allow researchers to complete field research and
analyze data for an ongoing study, and addressed agricultural
activities only through December 31, 2004. To ensure that our review of
the species' status was complete and based on the best available
scientific and commercial information, we requested comments on the
proposal to list the mountain plover as a threatened species, including
all information related to the species' status and the proposed
listing. We invited public comments on the proposed listing, new
information relevant to our consideration of the status of the mountain
plover, and comments and information regarding threats to the species
and its habitat.
Species Information
Our February 16, 1999, and December 5, 2002, proposed rules (64 FR
7587 and 67 FR 72396, respectively), and our September 9, 2003,
withdrawal of our 2002 proposal to list the mountain plover (68 FR
53083) described the species' life history, ecology, and habitat use.
For additional background on the natural history of the mountain
plover, see the account of the species in The Birds of North America
(Knopf and Wunder 2006).
While the majority of relevant information directly pertaining to
the mountain plover that has become available since our December 5,
2002, proposal to list (67 FR 72396) and September 9, 2003, withdrawal
of that proposal (68 FR 53083) has resulted from local or Statewide
studies on the mountain plover's breeding range; two recent documents
provide extensive review of current knowledge regarding the mountain
plover:
(1) Mountain Plover (Charadrius montanus) in Birds of North America
(Knopf and Wunder 2006); and
(2) Conservation Plan for the Mountain Plover (Charadrius
montanus), Version 1.0 (Andres and Stone 2009).
[[Page 27757]]
Numerous other recent documents are summarized in our June 29,
2010, notification reinstating our December 5, 2002, proposed rule to
list the mountain plover as threatened under the Act (75 FR 37353).
These include over twenty peer-reviewed journal articles, and many
other reports and summaries relevant to the status of the mountain
plover that have become available since 2002.
The following sections highlight and update information on the
mountain plover with emphasis on information developed since 2002.
Taxonomy and Species Description
The mountain plover (Charadius montanus) is a small bird in the
order Charadriiformes, family Charadriidae. No subspecies are
recognized. It is a migratory, terrestrial shorebird averaging 8 inches
(21 centimeters) in body length. Mountain plover are light brown above
and white below, but lack the contrasting dark breast band
characteristic of several other plovers such as the more common
killdeer (C. vociferus). Sexes are similar in appearance.
Feeding Habits
Mountain plover feed on ground-dwelling invertebrates and flying
invertebrates found on the ground, primarily beetles, crickets, and
ants. They forage with a series of short runs and stops, feeding
opportunistically as they encounter prey (Knopf and Wunder 2006,
unpaginated).
Breeding
Mountain plover return north to their breeding sites in the western
Great Plains and Rocky Mountain States in spring. They arrive at their
breeding grounds in northeastern Colorado in late March (Graul 1975, p.
6). Arrival is earlier farther south and later in Montana and at higher
elevations in South Park, Colorado (Knopf and Wunder 2006). Mountain
plover are territorial during the breeding season, with males defending
territories shortly after arrival (Knopf and Wunder 2006). Mountain
plover are generally monogamous; they form pairs and begin courtship on
arrival at their breeding grounds. Nests consist of a simple ground
scrape. Egg laying in northeastern Colorado begins in late April and
extends through mid-June (Graul 1975, p. 7). Graul (1973, p. 84)
described mountain plover nesting as a ``rapid multi-clutch system.''
The female normally produces two clutches, typically three eggs each,
at different nest sites; the male incubates the first nest site while
the female incubates the second. If the first nest or brood is lost
early in the breeding season, the adult may renest, so each pair can
potentially make four attempts per year to raise a brood. This breeding
system may increase breeding success given predation that occurs on
mountain plover nests or broods. This breeding system, rare among bird
species, may result in greater reproductive potential than in other
shorebirds (Knopf and Wunder 2006). It may have developed in response
to food fluctuations that typically occur in the shortgrass prairie,
where insect populations likely fluctuate in response to annual,
seasonal, and local fluctuations in precipitation (Graul 1973, p. 85).
Average incubation period is 29 days (Graul 1975, p. 19). Chicks
leave the nest within hours of hatching and obtain their own food. Only
one adult normally tends each nest and brood. The minimum habitat
requirement for mountain plover broods in Montana was 70 acres (ac) (28
hectares (ha)) (Knopf and Rupert 1996, p. 33), and brood home ranges
averaged 143 ac (57 ha) on rangeland in Colorado (Knopf and Rupert
1996, p. 31). Brood home ranges appeared similar for three Colorado
landscapes (Dreitz and Knopf 2007, p. 129). Parents stay with chicks
until they fledge, which occurs at about 33 to 34 days (Graul 1975, p.
25). Mountain plover breed their first spring and every year thereafter
(Knopf and Wunder 2006).
Habitat and Range
Although often thought of as a grassland species, the mountain
plover may best be described as a species of disturbed prairie or semi-
desert habitat (Knopf and Miller 1994, p. 505). They are found on open,
flat lands including xeric (extremely dry) shrublands, shortgrass
prairie, barren agricultural fields, and other sparsely vegetated
areas. On grasslands, they often inhabit areas with a history of
disturbance by burrowing rodents such as prairie dogs (Cynomys spp.),
native herbivores, or domestic livestock.
Mountain plover breed from Canada (extreme southern Alberta and
Saskatchewan) to northern Mexico (Figure 1) with greatest apparent
numbers in Colorado and Wyoming, and substantial numbers in Montana,
New Mexico, and Nebraska. In Mexico, breeding populations are suspected
in the States of Chihuahua, Cohuila, and Nuevo Leon (Andres and Stone
2009, p. 9).
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Mountain plover winter in similar habitat, many in California, but
also in southern portions of Arizona, Nevada, New Mexico, Texas, and in
northern Mexico. While California's Sacramento, San Joaquin, and
Imperial Valleys support the greatest documented concentrations of
wintering mountain plover, relatively little is known about wintering
numbers or distribution in other areas.
Breeding Habitat
Common elements of mountain plover breeding habitat include short
vegetation, bare ground, and flat topography. The mountain plover
historically nested in a region impacted by a variety of herbivores,
including prairie dogs, bison (Bison bison), and pronghorn antelope
(Antilocapra americana), because these heavily grazed or similarly
disturbed landscapes support reduced height and density of vegetation,
creating favorable breeding habitat for mountain plover. While the
mountain plover is categorized as a shorebird, it is seldom found near
margins of freshwater or marine estuaries. Dinsmore (2003, pp. 14-17)
described four types of breeding habitat: Short- and mixed-grass
prairie, prairie dog colonies, agricultural lands, and semi-desert.
[[Page 27759]]
On the plains, the mountain plover is generally considered an
associate of the shortgrass prairie, dominated by blue grama (Bouteloua
gracilis) and buffalo grass (Buchloe dactyloides) (Knopf and Miller
1994, p. 504). In the Pawnee National Grasslands (PNG) in northern Weld
County, Colorado, an area that formerly supported the greatest known
concentration of breeding mountain plover, breeding habitat was
described as restricted to flat, heavily grazed areas (Graul 1973, p.
69). Native prairie grasslands formerly presented a diverse ecosystem,
shaped by low precipitation, grazing, and fire. Today, prairie
landscapes often consist of grassland fragments where current cattle
grazing practices tend to create relatively uniform grass coverage and
height, which is not beneficial to mountain plover (Knopf 2008, pp. 55-
57). Typical range management practices such as rotational grazing,
limited grazing, and improving soil moisture are designed to promote
taller grasses that limit mountain plover use. Within these landscapes,
areas of cattle concentration (loafing areas and near water),
disturbance caused by prairie dogs, and plowed or fallow (unseeded for
one or more seasons) agricultural fields create conditions favorable
for mountain plover nesting (Knopf and Wunder 2006). Mountain plover
are also attracted to burned areas in their breeding grounds, and
burning may be valuable as a habitat management tool (Knopf 2008, pp.
25-26, 57-58, 61; Andres and Stone 2009, p. 34).
Prairie dog colonies create important habitat for mountain plover,
and are especially important to maintaining mountain plover populations
in the northern portions of their range (Dinsmore et al. 2003, pp.
1024-1025; Dinsmore et al. 2005, p. 1552; Augustine et al. 2008,
unpaginated; Childers and Dinsmore 2008, p. 705; Tipton et al. 2009,
pp. 496-497; Dreitz 2009, pp. 875-877). Active prairie dog colonies
provide exposed soils around burrows and, because prairie dogs keep
surrounding vegetation clipped, an area of low-growing, perennial
vegetation that is suitable as mountain plover breeding and brood-
rearing habitat. In addition, prairie dogs give alarm calls in response
to the approach of predators and may alert mountain plover to predator
presence. The density of mountain plover was found to be much greater
on black-tailed prairie dog (C. ludovicianus) colonies than on other
habitats in Montana (Childers and Dinsmore 2008, pp. 705-706). In
north-central Montana, the size of the adult mountain plover population
closely tracked annual changes in the area occupied by black-tailed
prairie dogs (Dinsmore et al. 2003, p. 1024). Both prairie dog and
mountain plover numbers declined sharply in the mid-1990s in response
to an outbreak of sylvatic plague, which caused deaths of prairie dogs
and resultant loss of favored mountain plover habitat. Mountain plover
later increased in concert with subsequent increases in prairie dogs
(Dinsmore et al. 2005, pp. 1550-1552).
In the Colorado shortgrass prairie ecosystem, mountain plover
densities observed on black-tailed prairie dog colonies were higher
than those on dryland agriculture and much higher than those on
grasslands without prairie dogs (Dreitz et al. 2006, p. 702; Tipton et
al. 2009, p. 496). Mountain plover were significantly more abundant on
black-tailed prairie dog colonies than on other rangeland within a
bison pasture in northeastern New Mexico (Groguen 2010, pers. comm.).
Prairie dog colonies occupied by mountain plover were, on average,
larger in size than colonies with no mountain plover. In Utah, mountain
plover nested in proximity to white-tailed prairie dog (C. leucurus)
colonies (Manning and White 2001, p. 226). In northeastern Mexico,
breeding mountain plover were associated with Mexican prairie dog (C.
mexicanus) colonies (Gonzales-Rojas et al. 2006, p. 82).
Mountain plover have been found to regularly use fallow or plowed
agricultural fields for nesting (Shackford et al. 1999, entire; Dreitz
and Knopf 2007, pp. 684-685; Bly et al. 2008, p. 127; McConnell et al.
2009, pp. 30-33). Where mountain plover have an opportunity to choose
between agriculture and prairie, they may use both equally (Knopf and
Rupert 1999, p. 84). Shackford et al. (1999, entire) found mountain
plover nesting on cultivated fields in Colorado, Oklahoma, Kansas, and
Wyoming. Fifty percent of all nests they encountered during their
research were on fallow or bare fields. While many nests were destroyed
by farm machinery, they concluded that mountain plover were using
cultivated fields successfully for nesting, especially in southern
portions of the species' range (Shackford et al. 1999, p. 117).
Recent studies addressed the mountain plover's nesting ecology, and
attempted to identify the extent of breeding distribution and
population size in Nebraska (Bly et al. 2008). They encountered 272
nests on agricultural fields of cultivated wheat and millet (Bly et al.
2008, p.123). Studies in Oklahoma encountered mountain plover on bare
agricultural fields (90 percent of observations), with few (5 percent
of observations) associated with prairie dog towns (McConnell et al.
2009, pp. 31-32).
It remains unknown whether Texas or Mexico crop fields support
mountain plover breeding (Andres and Stone 2009, p. 24). Holliday
(2010) reported that breeding season sightings of mountain plover from
the Texas Panhandle tended to be in cultivated fields as in adjacent
Oklahoma, although previously reported nesting in West Texas was in
grazed, short-grass habitat.
Knopf and Wunder (2006) described mountain plover as breeding
``more predictably'' at semi-desert locations west of the shortgrass
prairie in Colorado, Wyoming, and Montana. Beauvais and Smith (2003,
entire) developed a model of mountain plover breeding habitat in shrub-
steppe habitat of western Wyoming. They related favored patches of
mountain plover breeding habitat to poor soils, low precipitation, and
wind scour, features they predicted would persist over time, especially
on public lands. In such habitats, mountain plover are less dependent
on prairie dog colonies to create breeding habitat. A Wyoming study
located 55 mountain plover nests in grassland or desert scrub habitat
in six counties (Plumb et al. 2005a, p. 225). All nest sites were
grazed by ungulates with prairie dogs present at only 36 percent of
nest sites, mostly in grassland (Plumb et al. 2005a, pp. 226-227). In
Montana, Childers and Dinsmore (2008, p. 107) noted that sparsely
vegetated, hardpan clay flats provided nesting habitat.
In summary, mountain plover require short vegetation with some bare
ground on their breeding sites. In grasslands, this usually requires
disturbance, such as that provided by prairie dogs, cattle grazing,
fire, or farming. In semi-desert environments, breeding habitat may
persist without these forms of disturbance.
Migration and Wintering Habitat
Southbound migration of mountain plover is prolonged, with post-
breeding flocks numbering in the hundreds forming in late June with
some remaining on breeding areas until September or October (Bly et al.
2008, p. 123; Andres and Stone 2009, p. 10). Mountain plover migrate
southward across the southern Great Plains in late summer and early
fall to Texas, New Mexico, and Mexico, with many then traveling west to
California (Knopf and Wunder 2006). During spring migration, mountain
plover move from their
[[Page 27760]]
wintering sites in early March and proceed quickly to breeding sites in
eastern Colorado by mid-March and in Montana by mid-April (Knopf and
Wunder 2006). Mountain plover are generally thought to use habitats
similar to those on the breeding and wintering grounds during
migration. During migration, they have also been reported using
alkaline or mud soils, and sod farms (Knopf and Wunder 2006). Few
studies have been conducted on stopover habitat, and little is known
about stopover ecology or food resources exploited (Andres and Stone
2009, pp. 14, 21, 37).
In winter, mountain plover use habitats similar to those on their
breeding grounds. Mountain plover are found wintering in California
mostly on fallow and cultivated agricultural fields, but also on
grasslands and grazed pastures (Hunting et al. 2001, p. 39; Knopf and
Wunder 2006).
Throughout the Central Valley of California, the field types used
by mountain plover vary seasonally, from uncultivated lands in October
and November, shifting toward cultivated lands over the winter (Hunting
and Edson 2008, pp. 183-184). Mountain plover wintering in the San
Joaquin Valley of California used tilled fields, grazed pastures,
alkali flats, and burned fields, but they preferred native valley sink
scrub (low vegetation dominated by alkali-tolerant shrubs) and
nonnative grazed or burned grasslands over any of the more common
cultivated land types (Knopf and Rupert 1995, pp. 747-749). Winter
habitat availability in California's Carrizo Plain seems linked to a
combination of livestock grazing and precipitation, with heavy grazing
and dry conditions creating conditions most favorable to the mountain
plover. Giant kangaroo rat (Dipodomys ingens) precincts (colonies) are
also used, especially when wet years produce tall vegetation elsewhere
(Sharum 2010, pers. comm.).
Mountain plover exclusively used cultivated sites in the Imperial
Valley of California (Wunder and Knopf 2003, pp. 74-75). While
cultivated lands are abundant throughout the Imperial Valley, not all
provide suitable feeding habitat. Mountain plover were found to favor
irrigated farmland, including burned bermudagrass (Cynodan dactylon);
harvested, grazed, or sprouting alfalfa (Medicago spp.) fields; and
newly cultivated fields (Wunder and Knopf 2003, pp. 75-76; AMEC Earth
and Environment 2003, p. 12). Fallow fields were used mostly for
roosting, and melon and vegetable fields were rarely or never used
(Wunder and Knopf 2003, pp. 75-76). Insect availability, furrow depth,
size of dirt clods, and the vegetation on contiguous land parcels were
all believed to influence the suitability of agricultural fields to
mountain plover.
In California, annual climatic variability, especially abundant
rainfall, influences field conditions and can reduce mountain plover
use of traditionally occupied wintering sites. For example, mountain
plover became virtually absent from cultivated fields in the Imperial
Valley during the rainy winter of 2004-2005 (Knopf and Wunder 2006).
Movement patterns of wintering mountain plover in California are shown
to be highly variable, with birds on several occasions moving more than
34 miles (mi) (55 kilometers (km)) in a week (Knopf and Wunder 2006).
In Arizona, mountain plover winter on sod farms and grazed
pastures, and are observed using the same sites yearly. Their use of
farm fields and other potential habitats is generally unknown, and
these areas are rarely surveyed (Robertson 2010, p. 1). A few mountain
plover have wintered in recent years on mowed grasses at Gila Bend Air
Force Auxiliary Field (Mendelsohn 2010).
In Texas, winter reports of mountain plover were correlated with
barren fields and grazed pastures (Holliday 2010). In Williamson and
Bell Counties, Texas, mountain plover winter only on large, flat,
plowed fields, especially those with some corn or sorghum stubble
(Fennel 2002, p. 29). In the Texas coastal bend area (Nueces and San
Patricio Counties), wintering plover are largely limited to plowed
fields rather than grasslands or fallow fields, with mountain plover
often following tractors while feeding (Cobb 2009, pers. comm.).
Wintering mountain plover in Texas have also been reported using burned
fields (Knopf and Wunder 2006), sod farms (Cobb 2011, pers. comm.),
coastal prairies, and alkaline flats (Andres and Stone 2009, p. 12).
In Mexico, mountain plover are found wintering in grassland areas
with high densities of prairie dogs (both black-tailed and Mexican) and
on heavily grazed pastures (Andres and Stone 2009, p. 12; Macias-Duarte
and Panjabi 2010, pp. 5, 7). Consistent with other areas, open habitat
with low grass cover and sparse or no shrub cover are elements common
to areas used by mountain plover in Mexico. However, significant
mountain plover use of crop fields in Mexico has not been reported
(Macias-Duarte and Punjabi 2010, p. 7).
Wunder (2007) studied geographic population structure in mountain
plover through color-banding and stable isotope concentrations in
feathers. He concluded that there is widespread mixing of mountain
plover populations in winter and that birds may use alternate wintering
sites in different years (Wunder 2007, p. 118). While mountain plover
appear annually at some favored wintering sites, site fidelity by
individual birds appears low. Mountain plover can move long distances
and use various sites even within a given winter.
Survival, Lifespan, and Site Fidelity
A long-term study on mountain plover breeding grounds in Phillips
County, Montana, provides much of what is known regarding population
dynamics of the species. The annual survival rate of adult mountain
plover of both sexes in Phillips County ranged from 0.74 to 0.96 yearly
(Dinsmore 2008, p. 50). The annual survival rate for juvenile mountain
plover (survival to 1 year of age) was 0.06 at hatching, but for those
chicks that reached fledging age was 0.62 (Dinsmore 2008, p. 51).
Survival estimates did not account for permanent emigration (birds
surviving but returning in subsequent years to sites outside of the
study area), so the actual annual survival may have been higher.
Previous estimates of survival rates and of estimated mean lifespan
of 1.92 years (Dinsmore et al. 2003, pp. 1020-1021) supported our
December 5, 2002, conclusion that the mountain plover had a shorter
lifespan than other plovers (Charadriidae) (67 FR 72397) and that this
might impact its opportunity to reproduce. These conclusions
underestimated adult mountain plover survival. The longer study of the
same population over years with varying weather and habitat conditions
modified the earlier conclusions regarding the mountain plover's
longevity. Mountain plover of 5 to 7 years of age were frequently
encountered, and a longevity record over 10 years was established
(Dinsmore 2008, p. 52). Based on this additional research, survival
rates for mountain plover appear comparable to those reported for other
plovers, and the mountain plover is now considered a relatively long-
lived species (Dinsmore et al. 2010, unpaginated). We no longer believe
that the mountain plover's lifespan is a liability that could
contribute to the negative impact of natural or manmade events
affecting the species.
Mountain plover have a high nest survival rate compared to other
ground-nesting species (Dinsmore et al. 2010), but nest success in
mountain plover has varied greatly from study to study. Successful
hatching (of at least one egg) ranged from 26 percent (Knopf and
[[Page 27761]]
Rupert 1996, pp. 29-30) to 65 percent (Graul 1975, p. 18). Dinsmore et
al. (2002, pp. 3485-3486) found differences in nest success between
nests incubated by males (49 percent) and females (33 percent). Dreitz
and Knopf (2007, p. 684) found nest success of 37 percent with no
appreciable difference between nests on agricultural fields and on
native rangeland.
There have been relatively few studies of chick survival (hatching
to fledging) and results vary greatly. Dreitz (2009, p. 6) estimated
that 30-day survival of chicks of mountain plover from prairie dog
colony nesting habitat was 75 percent, and that 30-day survival on
other grasslands and on agricultural fields was less than 25 percent.
Following similar methodology, research on crop fields in Nebraska
found 95 percent survival of chicks accompanying 31 adult mountain
plover that were radio-tracked for the 36 days after eggs hatched
(Blakesley and Jorgensen 2010). Radio contact was lost with other
adults (due to birds leaving the area or transmitter failure), but even
if assuming all chicks associated with these adults perished, chick
survival was at least 58 percent (Blakesley and Jorgensen 2010). Dreitz
et al. (2010) studied post-hatching chick survival (hatching to
fledging) via radio-tracking in Colorado and Montana. The study
targeted factors affecting survival, including landscape
characteristics, with an objective of informing conservation and
management efforts. Field studies in 2010 were hampered by unusually
cold and wet weather. Of 93 chicks radio-tracked over three habitat
types in Colorado, only 9 were confirmed to survive to 30 days (Dreitz
et al. 2010, p. 3). Thirty-eight confirmed mortalities included 13 from
avian predators, 8 from mammalian predators, and 17 from unknown
predation, weather, and undetermined factors. Contact with other chicks
was lost, and their fates were unknown. Results did not reflect higher
chick survival on prairie dog towns than on other grasslands or
agricultural fields. In Montana, only 1 of 39 chicks monitored on
black-tailed prairie dog colonies was confirmed to survive to 30 days.
Nineteen mortalities were documented, with 13 from heavy rains (Dreitz
et al. 2010, p. 4). Sources of mortality differed among habitats in
Colorado, with avian predation higher at black-tailed prairie dog towns
(Dreitz et al. 2010, p. 6). However, results of the study are
considered preliminary, and future work is planned.
Few studies have estimated seasonal adult survival rates. Dreitz
(2010, unpaginated) found 89 percent survival of adults with broods for
the 30 days after hatching. A study of overwintering mountain plover in
California showed nearly 95 percent survival of wintering birds from
November 1 to March 15 (Knopf and Rupert 1995, p. 746). Since survival
of adults during stationary periods is believed to be relatively high,
and there is no estimate for adult survival during spring and fall
migration, there is potential that losses of adults during migration
may be significant and efforts to increase adult survival might be
focused on migration periods (Dinsmore et al. 2003, p. 1023; Andres and
Stone 2009, p. 1; Dinsmore et al. 2010). However, there is no
scientific information available to indicate that high mortality during
migration is occurring.
A life stage-specific model based on data from three breeding
areas, two in Colorado and one in Montana, found that mean adult
survival was the parameter that most influenced modeled population
growth (Dinsmore et al. 2010). The importance of adult survival was
characterized as typical of long-lived bird species, for which repeated
reproductive attempts throughout life are less important to population
growth, as evidenced by low chick survival, than adult survival
(Dinsmore et al. 2010). Nest survival was comparable to, or higher
than, other ground-nesting shorebirds and was less important to
population growth than survival of chicks, juveniles, and adults. Large
variation in estimates of chick survival led to the conclusion that to
improve population viability on breeding areas, management to increase
chick survival should be a priority. The authors believed such
management should be emphasized over past efforts to decrease nest
losses and increase hatching success (Dinsmore et al. 2010). However,
the authors conceded that management to improve chick survival is more
difficult than improving hatching success and might require large-scale
habitat improvement.
Mountain plover were thought to have high site fidelity to nesting
locations, returning to same area where they hatched each year (Graul
1973, p. 71). Skrade and Dinsmore (2010, p. 672) quantified mountain
plover dispersal on breeding sites in Montana and reported juvenile
(natal) dispersal (hatching year to return at age 1) averaged 8.1 mi
(13.0 km) for males and 6.3 mi (10.2 km) for females. Only 4 of 38
banded chicks returning as adults arrived back at the same black-tailed
prairie dog colony where they were banded. Knopf and Wunder (2006)
noted a chick that had dispersed over 30 mi (50 km) in Colorado.
The previous year's nesting success influences adult dispersal;
unsuccessful adults disperse farther than successfully breeding adults
(Skrade and Dinsmore 2010, p. 671). While adults rarely move far from
the area where they nested the previous year, evidence of potential for
year-to-year dispersal in adults is exemplified by an adult mountain
plover banded on a breeding area in Colorado in 2009, that was found
nesting approximately 25 mi (40 km) away in Nebraska in 2010 (Bly
2010b, pers. comm.).
Results from genetic studies suggest that gene flow among breeding
areas is sufficient to offset genetic effects of small populations and
reported adult fidelity to breeding areas (Oyler-McCance et al. 2008,
pp. 496-497).
Population Size and Trends
Mountain plover are difficult to detect because they are
cryptically colored and in general are widely distributed at low
densities (Knopf and Wunder 2006). Based on historical observations of
mountain plover and extensive habitat changes, there is general
agreement that the mountain plover is currently greatly reduced in
numbers and range compared to their numbers and range prior to European
settlement (Graul and Webster 1976, p. 265; Knopf and Wunder 2006). The
mountain plover's historical breeding range is believed to have
differed from that currently occupied primarily in its eastern extent,
which may have encompassed the western thirds of North Dakota, South
Dakota, and Nebraska, and more of western Kansas and the Texas
Panhandle than is currently occupied (Graul and Webster 1976, p. 265,
Knopf and Wunder 2008).
Population estimates for the species, both historical and recent,
appear imprecise. Graul and Webster (1976, p. 266) estimated that
mountain plover populations in Montana, Wyoming, eastern Colorado, and
New Mexico then totaled 214,200 to 319,220 birds, with 20,820 in the
population stronghold of Weld County, Colorado. However, Knopf and
Wunder (2008) cited Graul (pers. comm.) as saying that the estimates
may have been off (i.e., high) by an order of magnitude (a factor of
10).
Knopf (1996, p. 12) estimated the total population of mountain
plover to be about 8,000 to 10,000, based on a 1994 wintering survey in
California and on assumptions regarding proportion of the wintering
population observed (i.e., that only half of birds wintering in
California had been counted and that 1,000 to 3,000 birds wintered in
Texas and other areas). We cited this estimate in our
[[Page 27762]]
December 5, 2002, proposed rule (67 FR 72396). In our September 9,
2003, withdrawal of our proposed listing (68 FR 53083), we again cited
the Knopf estimate above and, using similar assumptions and newer
California winter survey data (1998-2002), provided a rangewide
estimate of 5,000 to 11,000 mountain plover. More recent studies, which
estimated populations present on specific portions of the breeding
range, have resulted in a higher rangewide estimate of the mountain
plover breeding population. After investigating Wyoming populations,
Plumb et al. (2005b, p. 15) estimated a minimum of 3,393 mountain
plover in Wyoming (up from previous estimates of 500 to 1,500) and
estimated a rangewide total of 11,000 to 14,000 mountain plover. Based
on newer information, including an upward revision of estimated
mountain plover numbers on the eastern Colorado plains (a conservative
estimate of 8,577 birds), Tipton et al. (2009, p. 497) provided a
rangewide estimate of 15,000 to 20,000 mountain plover. Andres and
Stone (2009, p. 8) reviewed available data and provided a coarse,
minimum rangewide estimate of 18,000 breeding mountain plover. Knopf
and Dreitz (in press) concluded that the continental breeding
population is ``certainly larger'' than the 17,500 birds estimated in
Montana, Wyoming, and Colorado, citing small populations in contiguous
States, a potentially significant population in New Mexico, and an
unknown population in Mexico. Based on our review of recent data,
including those from Nebraska (Van der Berg et al. 2010) and New Mexico
(see Breeding Range below), we estimate that the current rangewide
mountain plover breeding population exceeds 20,000 birds. This was
supported by Knopf (2009, pers. comm.). We have no information to
indicate that this estimate reflects an actual increase in rangewide
mountain plover numbers over previous, lower estimates. Instead, it
likely reflects the limitations of those earlier rangewide estimates
(based on mountain plover wintering in California that largely
discounted birds wintering elsewhere) and more accurate recent
estimates of breeding populations.
Accurate trend information for mountain plover numbers is generally
lacking. Interpreting trends from the two long standing surveys, the
Breeding Bird Survey (BBS) and the National Audubon Society's Christmas
Bird Count (CBC), suffer from a variety of problems, including the
inherent difficulties associated with using a survey of only a small
portion of a total population to infer rangewide trends (Knopf and
Wunder 2004, p. 1).
The BBS is a large-scale survey of North American birds that began
in 1966, and is conducted during the breeding season by observers
driving along roads over established routes. Knopf (1996, p. 12) cited
BBS data from 1966 through 1993 as indicative of a steep decline in
mountain plover numbers across their breeding range (3.7 percent per
year, a decline of approximately two-thirds over the period). However,
Knopf and Wunder (2004, p. 1) suggested that the timing of surveys
(which occur mostly in June when mountain plover are less conspicuous)
and the low densities at which mountain plover occur prevent reliable
trend estimates.
Based on recent BBS data analysis (Sauer 2010a), the mountain
plover has declined rangewide at an estimated rate of 2.6 percent per
year for the period from 1966 to 2009 (95 percent confidence interval
(CI) -6.7 to +0.6). However, for the period from 1999 through 2009, the
estimated rate of decline decreased to 1.1 percent per year (95 percent
CI -5.8, +9.6) (Figure 2). While neither estimate varies statistically
from a stable population (at a 95 percent CI), the probability that the
estimated long-term trend (1966 through 2009) is less than or equal to
zero is 95 percent. The probability that the estimated short-term trend
(1999 through 2009) is less than or equal to zero is 68 percent. The
estimated long-term decline is consistent with the generally accepted
conclusion that the mountain plover's rangewide population is currently
smaller than it was in the 1960s. The more recent (1999 through 2009)
estimated decline and associated CI lead us to conclude that most or
all of the long-term decrease took place before 1999, that any recent
declines are modest, and that the mountain plover population may be
near stable.
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Sauer (2011, pers. comm.) concluded that limited regional data from
the BBS (i.e., the low numbers of routes reporting the species and low
numbers of mountain plover observed) resulted in imprecise trend
estimates within individual States and for the time periods of
interest. He also concluded that BBS data only provide an imprecise
summary of mountain plover population dynamics, and the limited sample
size likely reflects the limitations of the roadside sampling frame in
sampling mountain plover breeding populations.
We conclude that, while the BBS is the only long-term trend
information available for the mountain plover on its breeding range, it
is an imprecise indicator of mountain plover population trends. Given
the wide confidence interval and the conclusion by Sauer (2011, pers.
comm.) above, the data provide limited support for any recent (1999
through 2009) trend in mountain plover numbers. Even so, we acknowledge
that this is the best available information on trends for this species
and BBS survey results suggest a recent (1999 through 2009) moderated
rate of decline (Figure 2). We provide long-term and recent BBS trend
estimates for three States where the sample size allowed for analysis
(see Conservation Status and Local Populations below), but with the
same reservations regarding precision.
The CBC is an annual count performed around the end of December in
which volunteers observe birds in 15-mi (24-km) radius count circles.
While CBCs can be used to infer species population trends, spatial
coverage is limited (Knopf and Wunder 2004, p. 1) and established count
circles commonly coincide with populated areas where volunteers are
available. The CBC data estimated an annual decrease of 2.8 percent in
mountain plover observed from 1966 through 2007, but reliability was
described as low (Butcher and Niven 2007, Appendix 1).
The vast majority of mountain plover reported in CBCs come from
California and, within California, from the South Salton Sea count.
Pandolfino (2009, unpaginated) submitted his analysis of CBC data for
California and recognized the data's limitations, but concluded that
the data reflected long-term and recent declines in mountain plover
numbers wintering in California. The CBC data on mountain plover
numbers is highly variable from year to year. The Salton Sea South CBC,
the only CBC in the Imperial Valley, is limited in scope and does not
include portions of the valley where most mountain plover have been
seen (Wunder and Knopf 2003, p. 76). Inherent limitations in data
collection methods (volunteers surveying small areas relative to total
winter range) and lack of sufficient detections of mountain plover in
California count circles (Hunting et al. 2001, p. 40) render trend
analysis uncertain. CBC data from other States and Mexico is even less
representative
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of wintering populations and provides no insight into possible trends
for the mountain plover.
We conclude, based on observations across the mountain plover's
range and BBS trend data, that a historical decline of the mountain
plover has occurred since the 1960s. However, we agree with the
conclusion of Andres and Stone (2009, p. 3) that precise and accurate
information on recent trends in mountain plover numbers is lacking. The
recent (1999 through 2009) decline estimate from BBS data is modest
(1.1 percent per year) and any difference from a stable population
estimate (slope of 0.0) is statistically insignificant. However, we
acknowledge that the BBS data is the best available information on
trends for the mountain plover and that BBS results suggest a recent
(1999 through 2009) moderated rate of decline (Figure 2). The CBC
wintering data are highly variable and come mostly from California, but
also suggest a long-term decline. No comprehensive trend data across
the mountain plover's wintering range are available. The discussion
below provides information on populations and trends within States,
Canada, and Mexico, where available.
Conservation Status and Local Populations
The mountain plover is listed as endangered in Canada, as a
sensitive species in Alberta, and as a threatened species in Mexico
(Andres and Stone 2009, p. 13; Gober 2010). The mountain plover is
identified by the Service as a Bird of Conservation Concern (Service
2008), is considered ``highly imperiled'' in the U.S. Shorebird
Conservation Plan (2004, p. 2), a category assigned to species listed
as threatened or endangered nationally, and all species with
significant population declines and either low populations or some
other high risk factor. It is also identified as ``G3-vulnerable'' by
NatureServe (2010). The species is listed as a sensitive species by the
U.S. Forest Service (USFS) (2010) and by the Bureau of Land Management
(BLM) (2000a, 2006, 2010a). It is identified as a species of global
conservation concern in the American Bird Conservancy and National
Audubon Watchlist, and it is listed as ``near threatened'' by the
International Union for the Conservation of Nature (IUCN) (BirdLife
International 2010). The designations discussed above may, in part,
reflect population estimates at the time those designations were
established. The IUCN previously (from 2004 to 2007) listed the species
as ``vulnerable,'' a higher level of concern than ``near threatened,''
but changed its rating as higher rangewide population estimates
emerged. The U.S. Shorebird Conservation Plan provided a rangewide
estimate of 9,000 mountain plover until 2006, when the estimate was
revised upward to 12,500 (Morrison et al. 2006, p. 69).
All States within the range of the mountain plover have included
the species in their Comprehensive Wildlife Conservation Strategy or
Wildlife Action Plans or both (State Plans) (Arizona Game and Fish
Department 2006; University of California 2005; Colorado Division of
Wildlife 2006; Wasson et al. 2005; Montana Fish, Wildlife and Parks
2005; Schneider et al. 2005; New Mexico Department of Game and Fish
2006; Oklahoma Department of Wildlife Conservation 2005; Texas Parks
and Wildlife 2005; Wyoming Game and Fish Department 2005) as either
``Species of concern'' or ``Species of greatest conservation need.''
Each State categorizes species under these designations based on
available information about the status, distribution, and trend of the
species in their State. They are not regulatory classifications, but
rather are intended to guide resource managers in making proactive
decisions regarding species conservation and data collection
priorities. The State Plans are not intended to be specific action
plans for any species. These designations do not result in any
protection for the species. However, the mountain plover is identified
as threatened in the State of Nebraska, the only State where the
species is listed as endangered or threatened.
Breeding Range
Colorado
In Eastern Colorado, the shortgrass prairie ecosystem provides
flat, dry breeding habitat for the mountain plover. The species
occupies grasslands within prairie dog colonies, grasslands without
prairie dog colonies, and dry land agricultural fields (Dreitz et al.
2005, pp. 129-130; Tipton et al. 2009, p. 496).
Knopf and Miller (1994, p. 504) noted the PNG, Weld County,
Colorado, as a breeding stronghold for the species, but in the mid-
1990s the population fell dramatically. The PNG now supports relatively
few breeding mountain plover. In 2009, Knopf provided an overview of
mountain plover studies on the PNG from 1986 through 2007. He suggested
that mountain plover numbers on the PNG had been in decline since the
late 1930s and early 1940s, and that the dramatic decline in the mid-
1990s was the abrupt endpoint of a process of deteriorating habitat,
exacerbated by other factors such as wet spring weather, increased
predation, and the relocation of breeding mountain plover to better
habitats elsewhere (Knopf 2008, p. 61).
Despite the virtual loss of the PNG population, over half of all
mountain plover are thought to breed in Colorado (Andres and Stone
2009, p. 15). A recent study reported a conservative estimate of 8,577
breeding mountain plover in eastern Colorado (95 percent CI 7,511 to
35,130) (Tipton et al. 2009, p. 497). A separate, higher elevation
population in South Park, Park County, Colorado, was estimated at 2,310
adults (Wunder et al. 2003, p. 661). Surveys through 2006 suggested a
stable population in South Park, with any variation largely
attributable to wet years and dry years affecting breeding conditions
(Wunder 2010a). Small numbers of mountain plover also occur in
Colorado's San Luis Valley (Hicks-Anderson and VerCauteren 2006,
entire). Andres and Stone (2009, p. 8) provided population estimates
for the United States, Canadian provinces, and Mexican States based on
their review of all available information. Their estimate of 11,000
mountain plover breeding in Colorado appears appropriate given
information available.
The BBS data from Colorado, 1966 through 2009 (-0.9 percent decline
annually, 95 percent CI (-7.0 to 3.5)) and 1999 through 2009 (0.3
percent increase annually, 95 percent CI (-5.5 to 14.7)) (Sauer 2010a),
suggest little long-term or recent change in breeding numbers in
Colorado. Based on these data, we conclude that the current breeding
population in Colorado, which likely supports half or more of all
breeding mountain plover, is relatively stable.
Wyoming
Wyoming has the highest estimated number of breeding mountain
plover outside of Colorado. The mountain plover is locally common and
has been detected in every county of Wyoming (Smith and Keinath 2004,
p. 3). A projected 20.5 million ac (8.3 million ha) of mountain plover
habitat exists in Wyoming, with 59 percent occurring on public lands
(Wyoming Natural Diversity Database (WYNDD) 2010; Emmerich 2010).
Nesting of mountain plover in Wyoming occurs in both grassland,
mostly in the eastern part of the State, and desert-shrub (Plumb et al.
2005b, p. 20). Mountain plover densities were comparable across habitat
types with overall density only slightly higher in grassland than in
desert-shrub (Plumb et
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al. 2005b, p. 20). Mountain plover appear to have less association with
prairie dog habitat in Wyoming than elsewhere (Plumb et al. 2005a, p.
226). Little of the mountain plover breeding range in Wyoming
(approximately 12 percent) is on cropland Knopf and Rupert 1999, p.
85).
Plumb et al. (2005b, pp. 19-20) estimated a minimum population of
3,393 mountain plover in Wyoming in 2002 and 2003. Andres and Stone
(2009, p. 8) provide an estimate of 3,400 mountain plover breeding in
Wyoming. This number is based on Plumb et al.'s estimate and, like that
estimate, it reflects the minimum number likely present. Given that
Plumb et al. (2005b, pp. 19-20) provided a conservative estimate, the
actual breeding population is likely larger; however, we have no basis
to provide a more accurate estimate.
The BBS data from Wyoming (Sauer 2010a), 1966 through 2009 (-1.2
percent decline annually, 95 percent CI (-5.7 to 3.3)) and 1999 through
2009 (-2.3 percent decline annually, 95 percent CI -13.9 to 4.5)),
suggest that both long-term and recent declines in breeding mountain
plover numbers in Wyoming may have occurred.
Montana
Primary breeding habitat for mountain plover in Montana is in the
north-central portion of the State where mountain plover are highly
dependent on black-tailed prairie dog colonies for habitat. Montana
Fish, Wildlife and Parks modeled suitable mountain plover habitat in
the State. Mapping indicated that the greatest area of highly suitable
habitat occurs in Phillips, Blain, Valley, and Fergus Counties with
patchy distribution though the central and southeast portions of the
State. The total area of suitable habitat estimated was 18.5 million ac
(7.5 million ha) (McDonald 2010).
Childers and Dinsmore (2008, p. 706) reported an estimate of 1,028
mountain plover in Phillips and Valley Counties in 2004 (95 percent CI
(903 to 1,153)). In 2010, standardized census areas in southwest,
central, and northeast Montana produced fewer sightings than previous
surveys (1992-2000, 2004); however, McDonald (2010) stated that results
were negatively influenced by above average rainfall, increased
vegetation height, and limited private land access; therefore, results
cannot be relied upon. Other than apparent confirmation of a previously
documented decline in the southwest census area (FaunaWest Wildlife
Consultants 2004, pp. 4-5), no trends could be inferred from the 2010
survey.
Andres and Stone (2009, p. 8) used the above estimate by Childers
and Dinsmore (2008, p. 706) and previous estimates of about 600
mountain plover elsewhere in Montana and provided a Statewide estimate
of approximately 1,600 mountain plover. BBS observations of mountain
plover on routes in Montana were insufficient to provide estimates of
population trend.
New Mexico
Most breeding season reports of mountain plover in New Mexico have
come from the northeast and western counties. Sager (1996, pp. 8-9)
found 152 presumed breeding adults at 35 sites in 11 counties in
northern New Mexico. Marguilies et al. (2004, p. 3) estimated 200
mountain plover in Union County alone throughout the summer and located
46 nests. In a limited effort, they also found 22 mountain plover and
six nests on public lands in Taos and Colfax Counties.
At BLM's North Unit, Taos County, point counts in 2005 through 2007
estimated 176 mountain plover on 8,400 ac (3,400 ha) of the 50,000-ac
(20,000-ha) unit considered to be favorable mountain plover breeding
habitat, based on past observation of mountain plover (Hawks Aloft
2007, pp. 9-11). If the entire unit was occupied at the same density,
an estimated 1,000 mountain plover might have been present on the North
Unit. Manderson (2010, pers. comm.) inspected habitat away from survey
routes in 2010, and suggested that, based on habitat quality, 500 or
more mountain plover could be present on the entire unit. Mountain
plover numbers seen on the same survey routes in 2010 were comparable
to those in earlier (2005 through 2007) surveys (Hawks Aloft 2010, p.
13), suggesting this population may be stable.
Goguen (2010, pers. comm.) estimated a minimum of 40 to 50 breeding
mountain plover on the Vermejo Ranch, Colfax and Taos Counties.
Mountain plover were also recently reported present in El Malpais
National Conservation Area, Cibola County (Hawks Aloft 2008, entire).
We found no Statewide breeding surveys or estimates of Statewide
breeding populations for mountain plover in New Mexico, other than
Andres and Stone's (2009, p. 8) conservative estimate of 500. Given the
above data from Union County, the BLM's North Unit in Taos County, the
Vermejo Ranch in Colfax and Taos Counties, and likely mountain plover
occurrence in several other counties, we believe that at least 1,000
and potentially significantly more mountain plover breed in New Mexico.
BBS data from New Mexico (Sauer 2010a), 1966 through 2009 (-5.0
percent decline annually, 95 percent CI (-8.6 to -1.2)) and 1999
through 2009 (-4.8 decline annually, 95 percent CI (-12.1 to 2.7)),
demonstrate a long-term decline and also suggest a short-term decline
in breeding mountain plover numbers in New Mexico. New Mexico is the
only State for which the long-term BBS trend statistically differs from
zero.
Nebraska
In our December 5, 2002, proposal to list the mountain plover we
estimated 200 mountain plover in Nebraska (67 FR 72399). Recent studies
attempted to identify the extent of breeding distribution and
population size in Nebraska (Bly et al. 2008, entire). Most nests were
found on agricultural fields in Kimball County, in extreme southwestern
Nebraska, but mountain plover were also found in nearby Cheyenne and
Blain Counties. The minimum breeding population was estimated to be 80
adults in 2007, based on nests found, and the total estimate of
breeding birds ranged upward to 360 (Bly et al. 2008, p. 127). Van der
Burg et al. (2010, pp. 50-53) reported on monitoring in the same three
counties (Kimball, Cheyenne, and Blain) in southwestern Nebraska and
estimated that mountain plover breeding numbers of 1,650, 1,617, and
1,558 over 3 years of the study (2005, 2006, and 2007, respectively).
The authors attributed past low estimates in Nebraska to: (1) Low
detection probabilities; (2) clumped spatial distribution of mountain
plover, which their estimation methodology corrected for; and (3)
``chronic undersampling.'' Given the above estimates from Van der Burg
et al. (2010, pp. 50-53), an estimate by Andres and Stone (2009, p. 8)
of 500 breeding mountain plover in Nebraska appears low.
Nebraska is the only State that has regulatory mechanisms in place
to conserve the mountain plover and its habitat, which likely protect
relatively few individuals. The Nebraska Game and Parks Commission
lists the mountain plover as a ``threatened'' species. Listing of
endangered and threatened species identifies those animals and plants
whose continued existence in Nebraska is in jeopardy. Efforts can then
be made to restore the species or to prevent extirpation or extinction.
Once a species is listed, a State law, titled the Nebraska Nongame and
Endangered Species Conservation Act, automatically prohibits take,
exportation, and possession, and imposes severe penalties on violators
(Nebraska Game and Parks Commission
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2011). Proposed projects that would be authorized, funded, or carried
out by Nebraska State agencies are reviewed as part of a mandatory
consultation process designed to prevent a State action from
jeopardizing the existence of an endangered or threatened species.
Recovery plans for endangered or threatened species are developed;
these recovery plans identify, describe, and schedule the actions
necessary to restore populations of these animals and plants to a more
secure status. Given that most mountain plover in Nebraska occur on
private agricultural lands, there are not many State projects that are
reviewed under the law. It is generally implemented only 4 or 5 times
per year, primarily on transportation, transmission, and energy
development projects (Lackey 2011, pers. comm.). While this law may
provide protection for some individual mountain plover in Nebraska, we
believe that it would only have minimal positive effects on the entire
population in Nebraska, or on the rangewide population.
Oklahoma
Recent studies to determine the breeding distribution and
population size in Oklahoma detected mountain plover in Cimarron and
Texas Counties in the Oklahoma panhandle, mostly on fallow or barren
agricultural fields (McConnell et al. 2009, pp. 30-33). Randomized
point counts were used to derive a Statewide population estimate of 68
to 91 birds (McConnell et al. 2009, pp. 32-33). Andres and Stone (2009,
p. 8) estimated 200 mountain plover breeding in Oklahoma. Given results
of McConnell et al. (2009, pp. 32-33), we believe that Andres and
Stone's (2009, p. 8) estimate may be slightly high. The range of the
mountain plover in Oklahoma was described as stable over the past 100
years, with the suggestion that populations may have changed little
(Hatcher 2010).
Kansas
The Kansas Department of Wildlife and Parks (2005) stated that
mountain plover breed only on dry upland in the shortgrass prairie of
western Kansas. While conversion to agriculture has left little native
breeding habitat, Cable and Seltman (2010, pp. 50-51) reported mountain
plover are an uncommon but regular breeding species in western Kansas
and that they also use idle cropland. Morton County may also serve as a
staging area for migration in late summer (Cable and Seltman 2010, p.
51). Andres and Stone (2009, p. 8) estimated 200 breeding mountain
plover in Kansas. No comprehensive surveys of breeding mountain plover
in Kansas have been attempted; however, given their apparent use of
both prairie and cropland, and a substantial population in nearby
Colorado, the estimate may be appropriate.
Texas
The mountain plover likely breeds in Texas, but there are no
confirmed reports of breeding since 1993 (Andres and Stone 2009, p.
16). Holliday (2010) described breeding season sight reports of
mountain plover from the Texas Panhandle near known Oklahoma breeding
sites. Holliday (2004) also mapped potential breeding habitat, much of
it on private land that has not been surveyed. Andres and Stone (2010)
did not provide an estimate of breeding mountain plover in Texas. We
believe that at least minimal numbers of mountain plover breed in
Texas.
Arizona
The only known mountain plover nesting in Arizona is in Apache
County in east-central portion of the State, with at maximum perhaps a
dozen breeding birds (Gardner 2010, pers. comm.). Breeding has occurred
on grasslands where cattle were concentrated and at Gunnison prairie
dog (C. gunnisoni) colonies (Corman 2005, pp. 591-591; Gardner 2010).
However, hundreds of square miles of potential breeding habitat in
northern and western Arizona have never been surveyed, and there are
reports of potential breeding mountain plover on Tribal lands in Navajo
County (Corman 2005, pp. 591-591; Gardner 2010, pers. comm.). Andres
and Stone (2009, p. 8) estimated 100 breeding mountain plover in
Arizona. This estimate acknowledges potential for a more substantial
breeding population than limited observations have documented.
Utah
The mountain plover has been a historically rare breeder in shrub-
steppe habitat in the Uinta Basin of northeastern Utah. Manning and
White (2001, p. 225) described a small breeding population that
averaged about 15 adults yearly. Mountain plover breeding in the area
subsequently declined, and no birds have been found during surveys of
the area since 2003 (Maxfield 2010, pers. comm.). Andres and Stone
(2009, p. 8) estimated fewer than 50 breeding mountain plover in Utah.
Based on no recent records of breeding mountain plover, this estimate
may be optimistic.
North Dakota and South Dakota
The mountain plover once bred in these States, with higher numbers
present in South Dakota, but there are no recent breeding records in
either North Dakota or South Dakota (North Dakota Game and Fish
Department 2010; South Dakota Game, Fish and Parks 2010).
Canada
A review of breeding records for Canada (Knapton et al. 2006, p.
33) concluded that the mountain plover is a peripheral species in
Canada with no evidence that it was ever a common or regular breeder.
The first breeding record was documented in 1979 and the most recent in
2007 (Knapton et al. 2006, pp. 32-33; Holroyd 2010, pers. comm.). Most
sightings and breeding records come from extreme southeastern Alberta,
with at least one incidence of confirmed breeding in Saskatchewan.
Holroyd (2010, pers. comm.) provided updated records of sightings
through 2009, mostly from Alberta. Andres and Stone (2009, p. 8)
estimated fewer than 100 mountain plover breeding in Canada. We are not
aware of any attempts to systematically survey all potential breeding
areas in the Canadian range. However, given the low number and limited
distribution of reported recent sightings (Holroyd 2010, pers. comm.),
we believe that actual breeding numbers are fewer than 100.
Mexico
Breeding records of mountain plover in Mexico have been documented
in southeastern Coahuila and Nuevo Leon, following a history of
breeding season observations in Mexican prairie dog colonies (Desmond
and Chavez-Ramirez 2002 entire; Gonzalez-Rojas 2006, pp. 81-84).
Nesting is suspected in San Luis Potosi, 130 mi (200 km) south of the
above records (Luevano et al. 20