Endangered and Threatened Wildlife and Plants; 12-Month Finding on a Petition to List Astragalus anserinus, 46521-46542 [E9-21754]
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the magnitude of risks in a project, and
to help the project sponsor predict and
establish a project budget and schedule.
The most important objective of risk
assessment and management protocols
is to help the project sponsor predict the
budget and schedule and to ensure that
the sponsor can complete the project
within the budget and schedule
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Project risks track the project
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• Requirements Risk. The first step in
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and
• Construction Risks. The final step is
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Once risks are identified, FTA and
project sponsors must determine the
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The preferred methods for managing
risk are avoidance, reduction, and
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not reduce risk, less preferred risk
management techniques include
increasing contingency, reducing project
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FTA works with each project sponsor to
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each project.
Project sponsors document this riskinformed management process in the
project management plan. Including
these strategies can help ensure that the
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strategies to avoid future delays.
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and technical capacity and capability,
and the project complexity or status.
C. Questions
1. Should FTA assign PMOCs to
oversee projects other than Major
Capital Projects? Please provide the
rationale for your recommendations
including how oversight of these
projects should alternatively be
provided if PMOCs are not utilized.
2. At what stage in the development
process should FTA assign PMOCs to
New Starts projects? Explain the basis
for your recommendation.
3. Other than a detailed review of a
grantee’s financial plan, what other
methods might FTA utilize to ensure a
grantee has the financial capacity to
construct and operate a major capital
project?
4. Please comment on FTA’s Risk
Management approach. If you do not
agree with FTA’s approach, please
recommend an alternative and provide
a basis for your recommendation.
Following the close of the comment
period on this ANRPM, FTA will
summarize and respond to the
comments and issue a Notice of
Proposed Rulemaking that posits
explicit text for a rewrite of the
regulation at 49 CFR Part 633. We
expect to publish such a Notice of
Proposed Rulemaking in 2009.
Issued this 4th day of September, 2009.
Peter M. Rogoff,
Administrator, Federal Transit
Administration.
[FR Doc. E9–21849 Filed 9–9–09; 8:45 am]
BILLING CODE P
DEPARTMENT OF THE INTERIOR
Fish and Wildlife Service
50 CFR Part 17
[Docket No. FWS–R1–ES–2009–0006]
[MO 922105 0082–B2]
Endangered and Threatened Wildlife
and Plants; 12-Month Finding on a
Petition to List Astragalus anserinus
(Goose Creek milkvetch) as
Threatened or Endangered
AGENCY: Fish and Wildlife Service,
Interior.
ACTION: Notice of a 12–month petition
finding.
SUMMARY: We, the U.S. Fish and
Wildlife Service (Service), announce our
12–month finding on a petition to list
Astragalus anserinus (Goose Creek
milkvetch) as a threatened or
endangered species under the
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46521
Endangered Species Act of 1973, as
amended (Act). After a thorough review
of all available scientific and
commercial information, we find that
listing A. anserinus under the Act is
warranted. However, listing is currently
precluded by higher priority actions to
amend the Lists of Endangered and
Threatened Wildlife and Plants. We
have assigned a listing priority number
(LPN) of 5 to this species, because the
threats affecting it have a high
magnitude, but are non-imminent. Upon
publication of this 12–month petition
finding, A. anserinus will be added to
our candidate species list. We will
develop a proposed rule to list A.
anserinus as our priorities allow. Any
determinations on critical habitat will
be made during development of the
proposed rule.
DATES: The finding announced in this
document was made on September 10,
2009.
ADDRESSES: This finding is available on
the Internet at https://
www.regulations.gov at Docket Number
FWS–R1–ES–2009–0006. Supporting
documentation we used to prepare this
finding is available for public
inspection, by appointment during
normal business hours at the U.S. Fish
and Wildlife Service, Utah Field Office,
2369 West Orton Circle Suite 50, West
Valley City, Utah 84119. Please submit
any new information, materials,
comments, or questions concerning this
finding to the above address or via
electronic mail (e-mail) at https://
www.fw1srbocomments@fws.gov.
FOR FURTHER INFORMATION CONTACT:
Larry Crist, Field Supervisor, U.S. Fish
and Wildlife Service, Utah Field Office
(see ADDRESSES)); by telephone at 801–
975–3330; or by facsimile at 801–975–
3331. If you use a telecommunications
device for the deaf (TDD), call the
Federal Information Relay Service
(FIRS) at 800–877–8339.
SUPPLEMENTARY INFORMATION:
Background
Section 4(b)(3)(B) of the Act (16
U.S.C. 1531 et seq.) requires that, for
any petition containing substantial
scientific and commercial information
that listing may be warranted, we make
a finding within 12 months of the date
of receipt of the petition on whether the
petitioned action is: (a) Not warranted,
(b) warranted, or (c) warranted, but
immediate proposal of a regulation
implementing the petitioned action is
precluded by other pending proposals to
determine whether species are
threatened or endangered, and
expeditious progress is being made to
add or remove qualified species from
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the Lists of Endangered and Threatened
Wildlife and Plants. Section 4(b)(3)(C) of
the Act requires that we treat a petition
for which the requested action is found
to be warranted but precluded as though
resubmitted on the date of such finding;
that is, requiring a subsequent finding to
be made within 12 months. We must
publish these 12–month findings in the
Federal Register.
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Previous Federal Actions
On February 3, 2004, we received a
petition dated January 30, 2004, from
Red Willow Research, Inc., and 25 other
concerned parties (the Prairie Falcon
Audubon Society Chapter Board,
Western Watersheds Project, Utah
Environmental Congress, Sawtooth
Group of the Sierra Club, and 21 private
citizens) requesting that we list
Astragalus anserinus as threatened or
endangered, emergency list the species,
and designate critical habitat
concurrently with the listing (Red
Willow Research Inc, in litt. 2004). We
acknowledged the receipt of the petition
in a letter to the petitioners in a letter
dated February 19, 2004. In that letter,
we advised the petitioners that our
initial review of the petition determined
that emergency listing was not
warranted, and that if conditions change
we would reevaluate the need for
emergency listing. We informed the
petitioner that in light of resource
constraints, we anticipated making our
initial finding in Fiscal Year 2005 as to
whether the petition contained
substantial information indicating that
the action may be warranted.
On August 16, 2007, we published a
notice of 90–day finding (72 FR 46023)
that the petition presented substantial
scientific or commercial information
indicating that listing A. anserinus may
be warranted, and that we were
initiating a status review of the species.
For more information, refer to the 90–
day finding that was published in the
Federal Register on August 16, 2007 (72
FR 46023). We received information
from the Bureau of Land Management,
Idaho Department of Fish and Game,
Red Willow Research Inc. (the
petitioner), and the Cassia County Weed
Control office in response to the 90–day
finding. All information received has
been fully considered in this finding.
In accordance with the President’s
memorandum of April 29, 1994,
Government-to-Government Relations
with Native American Tribal
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Governments (59 FR 22951), Executive
Order 13175, and the Department of the
Interior’s manual at 512 DM 2, we
readily acknowledge our responsibility
to communicate meaningfully with
recognized Federal Tribes on a
government-to-government basis. In
accordance with Secretarial Order 3206
of June 5, 1997 (American Indian Tribal
Rights, Federal-Tribal Trust
Responsibilities, and the Endangered
Species Act), we readily acknowledge
our responsibilities to work directly
with the Tribes in developing programs
for healthy ecosystems, to acknowledge
that Tribal lands are not subject to the
same controls as Federal public lands,
to remain sensitive to Indian culture,
and to make information available to
Tribes. In fulfilling our trust
responsibilities for government-togovernment consultation with Tribes,
we met with the Shoshone Paiute Tribes
regarding the process taken to conduct
a 12–month status review of Astragalus
anserinus. As an outcome of our
government-to-government
consultation, we recognize the strong
cultural significance of A. anserinus to
the Shoshone Paiute Tribes and
acknowledge that in this 12–month
finding. This notice constitutes the 12–
month finding on the January 30, 2004,
petition to list A. anserinus as
threatened or endangered.
Species Information
Astragalus anserinus was first
collected in 1982 by Duane Atwood
from a location in Box Elder County,
Utah, and subsequently described in
1984 (Atwood et al. 1984, p. 263). The
species is known only from tuffaceous
(ashy) soils found near Goose Creek on
the Idaho, Nevada, and Utah border, an
area approximately 20 miles (mi)(32.5
kilometers (km)) long and 4 mi (6.4 km)
wide. A. anserinus is a low-growing,
matted, perennial forb (flowering herb)
in the pea or legume family (Fabaceae),
with grey hairy leaves, pink-purple
flowers, and brownish-red curved seed
pods (Mancuso and Moseley 1991, p. 4).
This species is distinguished from A.
calycosus (Torrey’s milkvetch), A.
purshii (woollypod milkvetch), and A.
newberryi (Newberry’s milkvetch), the
three other mat-forming Astragalus
species found in the Goose Creek
drainage, primarily by its smaller
leaflets and flowers, as well as the color
and shape of the seed pods (Baird and
Tuhy 1991, p. 1; Mancuso and Moseley
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1991, pp. 4–5). In our August 16, 2007,
90–day finding (72 FR 46023), we used
the common name for the species,
‘‘Goose Creek milk-vetch.’’ Here we use
‘‘Astragalus anserinus’’ for accuracy,
and ‘‘Goose Creek milkvetch’’ (unhyphenated) to make the taxonomy
more consistent with today’s botanical
nomenclature.
Biology, Distribution, and Abundance
Astragalus anserinus typically flowers
from late May to early June. The species
is assumed to be insect-pollinated, but
the specific pollinators are unknown
(Baird and Tuhy 1991, p. 3). Fruit set
begins in early June with fruits
remaining on the plants for several
months. Mechanisms of seed dispersal
are also unknown, but may include
wind dispersion of seed pods and insect
or bird agents (Baird and Tuhy 1991, p.
3). Because A. anserinus often grows on
slopes and because the seed pods are
found close to the ground below the
vegetative portions of the plant, water or
gravity dispersal may also be a dispersal
mechanism. In 2004 and 2005, clusters
of seedlings were occasionally observed
on abandoned ant hills, which could
suggest some ant dispersal. Little
scientific research specific to A.
anserinus has been conducted beyond a
basic species description and various
survey efforts.
Limited information is available
regarding Astragalus anserinus
longevity. In September 2004, the U.S.
Bureau of Land Management (BLM)
Field Office in Burley, Idaho (BLMIdaho), permanently marked 10
seedlings in a wash at the base of a
tuffaceous outcrop (soils comprised of
volcanic ash and particulates) at one site
(Site 1), 8 seedlings and 7 adults at the
base of a slope at a second site (Site 2),
and 12 seedlings and 10 adults at a third
site (Site 3) (A. Feldhausen, Burley
BLM, in litt. 2007a, pp. 8–9). The results
of this effort are summarized in Table 1
below. In a separate monitoring effort,
BLM-Idaho conducted annual counting
of A. anserinus individuals at two sites
(Big Site 1 and Big Site 7) from 2004 to
2007. These results are depicted in
Table 2 below. In combination, these
two studies demonstrate large
fluctuations in the number of
individuals between years, with Table 2
reflecting almost a doubling or halving
in magnitude between the numbers of
individuals observed in successive
years.
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TABLE 1. SHORT-TERM TRACKING OF Astragalus anserinus INDIVIDUALS (2004–2006) (A. FELDHAUSEN, IN LITT. 2007A,
PP. 8–9).
Site 1
Site 2
Site 3
Year
Seedlings
Seedlings
Adults
Seedlings
Adults
2004
10 seedlings
8 seedlings
7 adults
12 seedlings
10 adults
2005
4 dead, 2 small
seedlings (15
leaves each), 4
small adult plants
with pods
6 dead, 1 small
seedling (12
leaves), 1 young
adult
1 dead, 6 alive
1 stake missing, 5
dead, 6 small
adults (3 with
pods)
1 dead, 9 with desiccated leaves and
numerous pods
2006
All 6 remaining plants
swept away by
water in a wash
Of the 7 remaining
adult plants, 2
dead and 5 alive
Of the 6 remaining
stakes: 1 stake
missing, 4 dead, 1
adult
7 dead, 3 stakes
missing
TABLE 2. MONITORING OF Astragalus
anserinus AT TWO SITES IN IDAHO
(A. FELDHAUSEN, IN LITT. 2007A,
PP. 8–9; IDAHO CONSERVATION
DATA CENTER (IDCDC) 2007A,
ELEMENT OCCURRENCE (EO) 003).
Big Site 1
Big Site 7
2004
123 total (2
dead, 73
seedlings,
48 adults)
138 total (42
seedlings,
96 adults)
2005
136 total (8
dead, 13
seedlings,
115
adults)
67 total (3
dead, 6
seedlings,
58 adults)
2006
88 total
135 total
2007
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Year
73 total
69 total
These wide-ranging fluctuations in
the number of Astragalus anserinus
individuals observed suggests that the
species is either short-lived or that adult
plants may remain dormant during
some growing seasons. If the species is
short-lived, corresponding
augmentation of seedlings to replace
lost individuals would be expected;
however, this has not been observed.
During spring census efforts, seedlings
(defined as young developing plants
having 3 or fewer leaves) made up 1,433
of the 30,281 individuals that were
counted in 2005 (4.7 percent), and 167
of the 4,087 individuals counted in 2008
(4.1 percent) (Service 2008a, p. 1). The
definition of seedlings used for
purposes of Table 2 is different than that
used in the 2004, 2005, and 2008 census
efforts; with seedlings in Table 2 being
defined by young developing plants
with cotyledons (the first leaves to
emerge from the ground) present.
Seedlings made up 59.3 percent of the
total individuals at Big Site 1 in 2004,
and 9.6 percent of the total individuals
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in 2005. Seedlings also made up 30.4
percent of the total individuals at Big
Site 2 in 2004, and 8.9 percent of the
total individuals in 2005 (J. Tharp,
Burley BLM, in litt., 2008a, p. 1).
Although we have no direct information
on A. anserinus seedling germination, it
would likely be more or less abundant
depending on the time of year sampled.
We expect spring would be the most
likely time to observe A. anserinus
seedlings, like many other plants, and
the seedlings could be more numerous
in years when climatic conditions are
more amenable to their germination and
establishment. One such climatic factor
could be annual precipitation; the
amount and timing of this precipitation
over the course of a year could influence
seed germination and seedling
recruitment.
During field surveys, several smaller
Astragalus anserinus plants were
partially excavated and observed to be
attached to large woody roots. Parts of
some individual plants frequently
appeared to be dead, with only a small
green portion remaining. This suggests
that vegetative growth may vary during
successive years, and that plant size
may not necessarily correspond to the
age of the individual. This also suggests
that some A. anserinus individuals may
remain dormant for an entire growing
season. In at least one other species of
Astragalus (A. ampullarioides), adult
plants can exhibit dormancy (an
inactive state) during a growing season,
and the perennial rootstock allows the
plant to survive dry years (Van Buren
and Harper 2003b in Service 2006a, p.
8). However, monitoring studies to
determine whether A. anserinus also
has this ability have not been
conducted.
Table 2 also demonstrates that
fluctuations in the number of Astragalus
anserinus individuals can vary across
sites during a given year. For example,
the number of individuals counted at
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Big Site 1 decreased from 136 to 88
between 2005 and 2006, whereas the
number of individuals counted at Big
Site 7 increased from 67 to 135 during
the same time period. However,
between 2006 and 2007, the number of
individuals counted at Big Site 1
decreased from 88 to 73 and the number
of individuals counted at Big Site 7
decreased 135 to 69. Since these sites
are approximately 0.5 mi (0.8 km) apart
on similar aspects, this suggests that
local weather patterns may not be a
predominant factor influencing plant
abundance and annual survival.
Although we acknowledge there are
some uncertainties with regard to
longevity, plant dormancy, and the
effect of climatic factors on A.
anserinus, the observed population
trend has been a decrease in the number
of observed individuals.
Astragalus anserinus is endemic to
the Goose Creek drainage in Cassia
County, Idaho; Elko County, Nevada;
and Box Elder County, Utah. The Goose
Creek drainage occurs within the Great
Basin ecosystem; this drainage receives
an annual rainfall average of less than
12 inches (30 centimeters). Element
Occurrences (EOs) are areas where a
species was or is recorded to be present.
The known EOs of A. anserinus occur
at elevations ranging between 4,900 to
5,885 feet (ft) (1,494 to 1,790 meters (m))
(Idaho Conservation Data Center
(IDCDC) 2007b, p. 2; Smith 2007, Table
1). Most A. anserinus EOs are within an
approximate 20-mi (32-km) long by 4-mi
(6.4-km) wide area, oriented in a
southwest to northeasterly direction
along Goose Creek. However one A.
anserinus EO has been documented
outside of the Goose Creek watershed
approximately 2 mi (3.2 km) south of
any other EOs. The geographic range of
the species has not been extended from
that presented in the 90–day finding (72
FR 46023; August 16, 2007). Based on
new information from surveys
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conducted in Nevada in 2006, during
which several new EOs were
discovered, gaps in the range have been
filled with the 6 new EOs extending
toward the 1 EO outside of the Goose
Creek drainage.
Astragalus anserinus occurs in a
variety of habitats, but is typically
associated with dry tuffaceous soils
from the Salt Lake Formation that have
a silty to sandy texture (Mancuso and
Moseley 1991, p. 12). In Utah, soil series
where A. anserinus has been located
include Bluehill fine sandy loam,
Codquin gravelly sandy loam,
Cottonthomas fine sandy loam, and
Tomsherry fine sandy loam (Hardy
2005, p. 4). The species has been
observed growing on steep or flat sites,
with soil textures ranging from silty to
sandy to somewhat gravelly. These
habitats can vary from stable areas with
little erosion to washes or steep slopes
where erosion is common. It appears
that the species tolerates, and may
proliferate with, some level of
disturbance, based on its occurrence on
steep slopes where downhill movement
of soil is common, within eroded
washes, and along road margins and
edges of cattle trails. However,
individuals have not been observed
where vehicle or livestock travel is
frequent or where water flows through
washes on a regular basis.
Astragalus anserinus is generally not
found on north-facing slopes, but is
found on most other slope aspects
within sparsely vegetated areas in
sagebrush and juniper habitats. The
estimated total plant cover (of all
species) at sites where A. anserinus
occurs is between 10 and 35 percent
(Hardy 2005, p. 4; Smith 2007, p. 2).
The dominant native species within the
general surrounding plant community
include Artemisia tridentata ssp.
wyomingensis (Wyoming big sagebrush),
Juniperus osteosperma (Utah juniper),
Chrysothamnus viscidiflorus (green or
yellow rabbitbrush), Poa secunda
(Sandberg’s bluegrass), and
Hesperostipa comata (needle and thread
grass). A. anserinus is frequently
associated with a suite of native species
that reside on the tuffaceous sand (Baird
and Tuhy 1991, pp. 2–3) including:
Achnatherum hymenoides (Indian
ricegrass), Chaenactis douglasii
(Douglas’ dustymaiden), Cryptantha
humilis (roundspike cryptantha),
Eriogonum microthecum (slender
buckwheat), Eriogonum ovalifolium
(cushion buckwheat), Ipomopsis
congesta (= Gilia congesta; ballhead
gilia), Mentzelia albicaulis (whitestem
blazingstar), and Phacelia hastata
(silverleaf phacelia). Several nonnative
species also co-occur with A. anserinus
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(see Nonnative Introduced Species
under Summary of Factors Affecting the
Species Rangewide: Factor A, below).
Another Goose Creek drainage endemic,
Penstemon idahoensis (Idaho
penstemon), is found near A. anserinus,
but these species are seldom found
immediately adjacent to one another.
Other sensitive species in the area
include Arabis falcatoria (= Boechera
falcatoria; falcate rockcress), and
Potentilla cottamii (Cottam’s cinquefoil)
(Franklin 2005, pp. 9–10, 159–160).
The Heritage/Conservation Data
Center programs in Idaho, Nevada, and
Utah rank Astragalus anserinus as a G2
species, indicating the species is
‘‘imperiled throughout its range because
of rarity or other factors that make it
vulnerable to extinction,’’ and S1
(critically imperiled) in the three states
(IDCDC 2007b, p. 2). Heritage/
Conservation Data rankings do not offer
any sort of protection, but are often used
to guide other agencies and entities in
designating sensitive species. The BLM
has assigned different status
designations to the species in the three
states where it occurs. In Idaho, A.
anserinus is designated as a type 2
species, which reflects a rangewide or
globally imperiled species with a high
endangerment status. In Utah, the
species is designated as a sensitive plant
species (Fortner 2003 in Franklin 2005,
p. 17), and in Nevada the species is
designated as a special status species
(Morefield 2001, p. 1). BLM policy
provides that species which are
designated as a ‘‘sensitive species’’ shall
be protected as candidate species for
listing under the Act (BLM 2001, p.
06C1).
Astragalus anserinus is currently
known from 19 EO records (5 in Idaho,
10 in Nevada, and 4 in Utah) (IDCDC
2007b, p.4; Smith 2007, p. 1; Utah
Conservation Data Center (UCDC) in litt.
2007, map; Service 2008b, 17 pp.). The
number of currently known EOs (19)
differs from the 24 EOs identified in the
90–day finding published on August 16,
2007 (72 FR 46023). Recently published
NatureServe guidelines for designating
EOs in Idaho and Utah (IDCDC 2007b,
p. 1; R. Fitts, Utah Conservation Data
Center, in litt. 2008, p. 1) state that sites
(occupied points, lines, or polygons)
that occur within 0.6 mi (1 km) of each
other are within the same EO.
Accordingly, several occupied sites that
were designated as individual EOs in
our August 16, 2007, 90–day finding
were combined. In addition, six new
EOs were discovered in Nevada as a
result of survey efforts in 2006. We
developed a naming convention to help
us manage and compare EO data for
recently consolidated sites before and
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after implementation of the NatureServe
guidelines. For example, the designation
U001–4–17 identifies Utah EO 001,
which was previously identified as Utah
EO 004. The suffix 17 reflects a site
number that has been assigned
according to the sequence the site was
counted in 2004 or 2005. We use our
naming convention as described, as well
as EO number in various places
throughout this finding, depending on
the context of the particular site being
referenced.
The majority of Astragalus anserinus
sites in Idaho, Utah, and Nevada occur
on Federal lands managed by the BLM
(Service 2008, 17 pp.). In 2004 and
2005, we conducted a multiagency
census and survey effort for A.
anserinus with the BLM, USFS, and
natural resource agencies from the
States of Idaho, Nevada, and Utah. Our
objective was to count (census) known
sites, survey additional areas, and
document any new populations. In
2004, we examined 33 sites in 5 EOs in
Idaho (3,467 individuals were counted);
6 sites in 3 EOs in Nevada (2,252
individuals were counted); and 11 sites
in 2 EOs in Utah (7,558 individuals
were counted) (Service 2008, 17 pp.). In
2005, we examined 5 sites at 1 EO in
Nevada (3,074 individuals were
counted), and 64 sites in 1 EO in Utah
(27,207 individuals were counted)
(Service 2008, 17 pp). During the 2004
and 2005 census efforts, 40,858
individual plants of the estimated
60,000 individual plants range-wide (68
percent) were counted at 119 sites in 12
EOs.
Estimating the total Astragalus
anserinus population size is
complicated because of the variability in
the species annual abundance, and the
different census and survey methods
that have been employed. For example,
plant abundance at one site in Idaho
over a 4–year period varied
significantly: 138 plants were counted
in 2004; 67 plants in 2005; 135 plants
in 2006; and 69 plants in 2007 (Service
2008, 17 pp.). Census efforts in 2008 at
3 sites that were not affected by a
significant wildfire in 2007
demonstrated a general decrease from
plant counts when compared to the
2004 or 2005 data; 1 site increased by
5.4 percent (652 to 687), 1 site decreased
by 76.3 percent (1,458 to 346), and 1 site
decreased by 79.0 percent (3,081 to 647)
(Service 2008c, Table 2). Using the best
available data for each A. anserinus site,
we estimate that there were
approximately 60,000 individuals
distributed across the three states prior
to the 2007 wildfires (Service 2008, 17
pp.). However, we recognize the
inherent variability associated with
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estimating population size, because of
large fluctuations observed between
successive monitoring years and the
differing census and survey methods
that have been employed. Generally, the
2004 and 2005 census counts yielded
higher numbers than had been
estimated by previous surveys (Service
2008, pp. 1–6), however, monitoring
efforts have not occurred regularly
enough or over a long enough period to
allow us to statistically analyze
population trends.
Based on pre-2007 (pre-wildfire)
individual plant count data,
approximately 10 percent of all known
Astragalus anserinus individuals occur
in Idaho (5,500 plants), 25 percent occur
in Nevada (15,500 plants), and 65
percent occur in Utah (39,000 plants)
(Service 2008c, Table 1). State-specific
information on the population status of
A. anserinus is described below.
Idaho
Prior to 2004, seven EOs (which are
now combined into four EOs under the
NatureServe guidelines) were monitored
by the IDCDC, who reported the number
of Astragalus anserinus individuals at
most sites as estimations. The first A.
anserinus EO was documented in 1985
(1 year after the species was described
(Atwood et al. 1984, p. 263)), but
systematic or comprehensive surveys
were not conducted in Idaho until 1991
(Mancuso and Moseley 1991, p. iii). In
1991, the A. anserinus population in
Idaho was estimated at over 914
individuals (Mancuso and Moseley
1991, pp. 2, 13–14).
During the 2004 census effort, the four
known Astragalus anserinus EOs in
Idaho were revisited and three new sites
were located (two sites were within an
existing EO and one new site was
considered to be a new EO). In total,
5,052 A. anserinus individuals were
counted, with 2,460 of these individuals
observed within the original 4 Idaho
EOs (Service 2006b, Table 1). Based on
pre-2007 EO revisions, census data from
2004 indicated: (a) stable plant numbers
at four EOs; (b) an increase in plant
numbers at one EO (compared to pre2004 survey numbers); and (c) an
unknown change at two EOs
(participants were unable to conduct a
complete census because part of the EOs
are on private property) (Service 2006b,
Table 1). However, because of the
different survey methodologies
employed before 2004, it is difficult to
conclusively compare survey and
census results or estimate long-term
population trends for A. anserinus in
Idaho (Service 2006b, Table 1).
In 2007, the IDCDC standardized its
methodology for designating Astragalus
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anserinus EOs to conform to the above
referenced NatureServe guidelines.
Under the new methodology, the four
existing EOs and the three new sites
found in 2004 were combined into five
EOs (EOs 1, 6 and 7 were deleted and
added to EO 3; EO 9 was added as a new
EO (IDCDC 2007b, p. 4)). The IDCDC
methodology also ranks the health of the
EOs based on a weighted formula made
up of three elements: EO size (33
percent); EO condition (based on the
abundance of native plants, introduced
plants, and anthropogenic disturbance)
(33 percent); and EO landscape context
(based on the degree of habitat
fragmentation) (33 percent). Rankings
are categorized from A through D, with
‘‘A’’ ranked EOs generally representing
higher numbers of individuals and
higher quality habitat, and ‘‘D’’ ranked
EOs generally representing lower
numbers of individuals and lower
quality (or degraded) habitat. Under this
ranking system, the IDCDC assigned an
‘‘A’’ ranking to one EO, ‘‘B’’ rankings to
two EOs, and ‘‘C’’ rankings to two EOs
(IDCDC 2007b, p. 4).
Monitoring efforts and results in
Idaho that have been used to inform this
status assessment for Astragalus
anserinus include: (a) the collection of
plant community data and
establishment of photo-points in 2000
and 2001 at 3 sites (Mancuso 2001a, pp.
8–9; Mancuso 2001b, p. 2); (b) census
efforts at all Idaho EOs on public land
in 2004 (Service 2008b, 17 pp.); (c)
conducting annual census efforts at 2
sites in Idaho since 2004, as
summarized in Table 2 above (A.
Feldhausen, in litt. 2007a, pp. 8–9;
IDCDC 2007a, EO 003); (d) the
permanent marking and monitoring of
A. anserinus individuals at 3 sites from
2004 to 2006 as summarized in Table 1
(A. Feldhausen, in litt. 2007a, pp. 8–9);
and (e), establishing A. anserinus –
Penstemon idahoensis – Euphorbia
esula (leafy spurge) control study plots
at 11 sites in 2007 by BLM-Idaho (A.
Feldhausen in. litt. 2007a, p. 3).
Nevada
Astragalus anserinus surveys in
Nevada were first conducted in 1991
and 1992, resulting in the
documentation of 4 EOs, with an
estimated plant abundance of 827
individuals (Morefield 2001, p. 1).
Subsequent census efforts in 2004 and
2005 failed to locate any new sites until
2006, when 6 new EOs with
approximately 11,000 individuals were
discovered. The 6 new EOs represent
18.3 percent of the estimated range-wide
population total of 60,000 individuals
(Service 2008b, 17 pp.). There are
presently ten known EOs in Nevada, as
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documented by the Nevada Natural
Heritage Program (NNHP) (Smith 2007,
p. 1). Site visits to 4 EOs were
conducted during the 2004 and 2005
census efforts, and 4,930 A. anserinus
individuals were counted. However,
because of the different survey
methodologies employed prior to 2004,
it is difficult to conclusively compare
survey and census results or estimate
long-term population trends for the
species in Nevada (Service 2006b, Table
1). In 2008, we counted individuals at
two sites during our post-2007 wildfire
assessment study, including EO 001
(which partially burned), and site 1 of
EO 004 (which did not burn). We
observed that the number of individuals
in EO 001 decreased by 68 percent,
while the number of individuals in EO
004 increased by 5.4 percent (Service
2008c, Table 2) (see the discussion
under Wildfire below for further details
on the 2008 study).
Monitoring efforts and results in
Nevada that have been used to inform
this status assessment include census
efforts conducted in 2004 and 2005 at
four EOs (Service 2008b, 17 pp.), and
post-wildfire census efforts in 2008 at
two EOs (one that partially burned, and
one that did not burn) (Service 2008c,
Table 2, Map 2).
Utah
There were 9 known Astragalus
anserinus EOs in Utah with an
estimated 7,617 individuals, based on
the results of initial surveys conducted
in 1990 and 1991 (Baird and Tuhy 1991,
p. 2; Morefield 2001, p. 1). Eight of these
EOs were documented by the UCDC,
and one EO was documented in the
Nevada Natural Heritage Program
database, although it was not reflected
in the UCDC database (Mancuso and
Moseley 1991, p.2). There were
additional Utah surveys in 1993 (Hardy
2005, p. 4), however we do not know
whether they were resurveys of known
sites and do not believe the results are
included in the UCDC database. The
BLM Salt Lake City, Utah field office
(BLM-Utah) staff indicates that they are
aware of data from at least one
additional site that has not been
submitted to the UCDC (Hardy 2005, p.
4). In addition, surveys were conducted
in Utah by BLM in 2000, 2001, and 2004
to evaluate the environmental effects of
a waterline and livestock water tank
construction project to the species
(Hardy 2005, p. 5); no sensitive plants
were discovered along the proposed
water line.
Site visits conducted to what was
then 6 known EOs, and 1 new site
during 2004 and 2005 census efforts
recorded a total of 33,476 Astragalus
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anserinus individuals, although only
partial plant counts were conducted at
3 of the 6 known EOs. Two other
documented EOs that had the greatest
numbers of individuals weren’t counted
during the 2004 and 2005 census efforts
because of limitations on access and
time constraints (Service 2006b, Table
1). The 2004 and 2005 census data
indicated higher A. anserinus count
numbers than the previous estimates at
five of the known EOs. However,
because of the different survey
methodologies that were used before
2004, we are unable to conclusively
compare survey and census results or
estimate long-term population trends for
the species in Utah (Service 2006b,
Table 1).
In early 2007, the UCDC reconfigured
Astragalus anserinus EOs in Utah to
conform to the general EO standards
guidebook, IDCDC methodology, and
NatureServe guidelines, resulting in the
combining of the nine previously
documented EOs into four EOs (R. Fitts,
in litt. 2008). Based on 2005 census
estimates, the largest Utah EO (EO 001)
supported over 37,000 plants, making
up over 60 percent the known
individuals range-wide (Service 2008b,
17 pp.).
In 2008, re-census efforts were
conducted as part of a post-wildfire
assessment at ten sites in Utah where
we had information on the number of
individuals from 2004 or 2005 surveys.
We surveyed two sites that did not burn,
four sites that were partially burned,
and four sites that were completely
burned. At the 2 sites that did not burn,
the individual numbers of plants
decreased by 76.3 percent and 79
percent. At the 4 sites that partially
burned, the individual numbers of
plants decreased by 34.9 percent, 89.7
percent, 91.1 percent, and 92.6 percent.
The individual plant counts at the 4
sites that completely burned decreased
by 94.9 percent, 98.1 percent, 98.2
percent, and 100 percent (Service 2008c,
Table 2) (see the Wildfire discussion
under factor A, below, for further
information on the 2008 post-wildfire
assessment efforts).
Monitoring efforts and results in Utah
that have been used to inform this status
assessment include: (a) census efforts
conducted in 2004 and 2005 at portions
of 2 EOs (Service 2008b, 17 pp.); (b)
installation of 4 small chicken-wire
exclosure cages over 5 individual plants
in 2004 to monitor effects of a waterline
construction project (all individuals
were still present in 2007) (Hardy 2008,
pp. 1–2); (c) documentation of 2
individual plants within a 300-foot long
belt transect in 2006 (scheduled to be
resurveyed in 2010 (Hardy 2008, p. 2));
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(d) establishing a study plot in 2007
near a waterline constructed in 2004
that includes 231 A. anserinus
individuals, which may be fenced in the
future (Hardy 2008, p. 1); and (e)
conducting field inspectionsat 10 sites
during the 2008 post-wildfire re-census
effort (Service 2008c, Table 2, Map 2).
Summary of Factors Affecting the
Species Rangewide
Section 4 of the Act (16 U.S.C. 1533)
and implementing regulations at 50 CFR
424, set forth procedures for adding
species to the Federal Lists of
Endangered and Threatened Wildlife
and Plants. Under section (4) of the Act,
we may determine a species to be
endangered or threatened based on any
of the following five factors: (A) The
present or threatened destruction,
modification, or curtailment of habitat
or range; (B) overutilization for
commercial, recreation, scientific, or
educational purposes; (C) disease or
predation; (D) the inadequacy of
existing regulatory mechanisms; or (E)
other natural or manmade factors
affecting its continued existence. In
making this finding on a petition to list
Astragalus anserinus, information
regarding the status of, and threats to, A.
anserinus in relation to the five factors
provided in section 4(a)(1) of the Act is
discussed below.
Factor A. The Present or Threatened
Destruction, Modification, or
Curtailment of Its Habitat or Range
Wildfire
Organisms adapt to disturbances such
as historical wildfire regimes (fire
frequency, intensity, and seasonality)
with which they have evolved (Landres
et al. 1999, p. 1180), and different rare
species respond differently to wildfire
(Hessl and Spackman 1995, pp. 1–90).
In general, fire regimes within forest and
steppe habitats in the western United
States have been highly disrupted from
historical patterns (Whisenant 1990, pp.
4–10; D’Antonio and Vitousek 1992, pp.
63–87; Weddell 2001, pp. 1–24). In
some instances, fire suppression has
allowed grasslands to be invaded by
trees (Burkhardt and Tisdale 1976, pp.
472–484; Lesica and Martin 2003, p.
516), and in many grassland and shrub
habitats, fire frequencies have increased
due to the expansion and invasion of
annual nonnative grasses (Whisenant
1990, pp. 4–10; D’Antonio and Vitousek
1992, pp. 63–87; Hilty et al. 2004, pp.
89–96). These invasive annual
nonnative grasses become established in
unvegetated areas that would normally
separate native vegetation, dramatically
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increasing the ability of wildfire to
spread.
Our understanding of the historical
wildfire regime in the Goose Creek
drainage, and specifically within
Astragalus anserinus habitat, is limited.
In general, the average wildfire return
interval within the sagebrush-steppe
ecosystem as a whole has been reduced
from between 60 and 110 years, to often
less than 5 years (Whisenant 1990, p. 4;
Wright and Bailey 1982, p. 158; Billings
1990, pp. 307–308; USGS 1999, pp. 1–
9; West and Young 2000, p. 262). Recent
wildfires often tend to be larger and
burn more uniformly across the
landscape, leaving fewer unburned
areas, which can affect the post-fire
recovery of native sagebrush-steppe
vegetation (Whisenant 1990, p. 4; Knick
and Rotenberry 1997, pp. 287, 297;
Brooks et al. 2004, pp. 682–683). The
result of this altered wildfire regime has
been the conversion of vast areas of
sagebrush-steppe ecosystem into
nonnative annual grasslands (USGS
1999, pp. 1–9). The proportion of
annuals in the sagebrush-steppe
ecosystem increases dramatically at
higher fire frequencies, while all other
vegetative life forms decrease.
Sagebrush can reestablish from seed
following fire, however the seeds are
short-lived and if a second fire occurs
before the new plants produce seed (4
to 6 years), the species may face local
extirpation. This would be less of a
problem if the fires occurred over
relatively small areas, because seed from
adjacent unburned areas would be
naturally transported back into burned
areas. As fires become larger, the
opportunity for seed migration into
burned areas is dramatically decreased
(Whisenant 1990, p. 8–9). Based on our
observations, Astragalus anserinus
seedling germination does not appear to
be stimulated by wildfire. Accordingly,
fewer individuals and fewer seeds
would be available for recruitment if
wildfire were to return before the
species is able to recover from earlier
wildfire impacts to the population. As a
result, there would be a corresponding
decline in the overall number of
individuals.
Wildfire was not documented within
Astragalus anserinus habitat prior to
2000 (A. Feldhausen, in litt. 2007, p. 3;
R. Hardy, Salt Lake City BLM, in litt.
2008, p. 1), although undoubtedly they
occasionally occurred in the past.
Astragalus anserinus habitat is normally
sparsely vegetated (e.g., typically 10 to
30 percent total vegetative cover), which
likely makes it less vulnerable to
wildfire because of the lack of fuels to
sustain fire over large areas. We are
aware of a wildfire that occurred in A.
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anserinus habitat in Idaho in 2000, and
another wildfire that occurred in
Nevada and Utah in 2007. The 2000
Idaho wildfire affected two EOs (EO 007
and EO 009), however at the time, EO
009 had not been documented and A.
anserinus was not affected by the 2000
wildfire at EO 007 (A. Feldhausen, in
litt. 2007a, p. 11). Accordingly, before
2008, we had no pre-wildfire data with
which to assess the impact of wildfires
on A. anserinus. Our knowledge of the
effects from wildfire was limited to
observations at EO 009 from 2004.
Based on the best available information,
EO 009 is made up of 3 separate
occupied sites that contain 10, 36, and
749 individuals based on 2004 surveys/
census efforts. The EO 009 site with 749
individuals is within a sparsely
vegetated slope with mature junipers
and shrubs, and may not have burned
during the 2000 wildfire.
Based on pre-fire data, a single
wildlfire in 2007 in Nevada and Utah
completely burned 3 EOs and portions
of 5 other EOs containing approximately
53 percent of all known Astragalus
anserinus individuals (31,500 of 60,000
individuals). The 2007 wildfire also
burned 25 percent of the known
occupied habitat (100 acres (ac) (41
hectares (ha)) out of an estimated 400 ac
(164 ha)) (Service 2008c, Table 1).
In Nevada, 3 EOs were completely
within the burned area footprint (1,512
total individuals), and three other EOs
were partially burned, but had an
estimated loss of approximately 72
percent of the individuals within those
3 EOs (5,394 of 7,508 individuals). In
Utah, portions of two EOs were burned
in the wildfire (EOs 001 and 009). The
wildfire in EO 001, which contained
more than 60 percent of the known
individuals (37,000 of 60,000
individuals), was estimated to have
burned approximately 40 percent of the
known individuals (24,000), and
approximately 18 percent of the total
occupied acreage (71 ac (29 ha)) (Service
2008b, 17 pp.). Please note that since six
of the 10 currently known EOs in
Nevada were not discovered until 2006
(EOs 005 through 010), and only
population estimates and point data
have been collected, the total number of
individuals and the acreage affected by
the 2007 wildfire are only estimates.
Estimating the number of individuals
and acres with greater precision is
difficult because of the various methods
that have been employed by prior
survey and census efforts.
Based on initial field visits and
reports following the 2007 wildfire
(Howard 2007, pp. 1–2), we initially
understood that the wildfire burned
intensely and almost continuously
across the landscape. However, our
2008 field inspection determined that
the wildfire burned as a mosaic rather
than continuously, and did not affect
some small patches of Astragalus
anserinus occupied habitat. We
observed that 21.3 percent, 81.1 percent,
and 94.6 percent of the total acreage was
burned at 3 A. anserinus sites, however
estimates were not made for 2 other
sites within the burned area perimeter
that were only partially burned (Service
2008c, Table 2). Our inspection also
documented the bunchgrasses
Hesperostipa comata (needle and
thread), Poa secunda (Sandberg’s
bluegrass), Pascopyron smithii (western
wheatgrass), Agropyron cristatum
(crested wheatgrass), and Achnatherum
hymenoides (Indian ricegrass), as well
as the shrub Chrysothamnus
viscidiflorus (green or yellow
rabbitbrush) re-sprouting from roots that
survived the 2007 wildfire. These
species generally made up
approximately 20 percent of the total
vegetative cover at the burned sites, and
it was estimated that 75 to 90 percent of
the bunchgrasses had survived the
wildfire (M. Mancuso, Mancuso
Botanical Services, in litt. 2008, p. 1).
In June, 2008, we conducted postwildfire re-census efforts to specifically
evaluate the effects of the 2007 wildfire
and determine the response of
Astragalus anserinus to this event. We
counted individual plants at 12 sites
where we had count data from either
2004 or 2005, including Nevada EO 001,
Nevada EO 004, and 10 sites within
Utah EO 001 (which represents the
largest EO). Three of the sites that were
surveyed were not burned, 5 of the sites
were partially burned (including Utah
EO 001–4–17 which supported 7,486
individuals prior to the fire based on
2005 data), and 4 of the sites were
completely burned. Using pre-2007
information, we estimate that we
resurveyed habitat containing
approximately half of the estimated
31,500 individuals burned in the 2007
wildfire (Service 2008c, Tables 1 and 2).
Generally, individual plant counts in
almost all burned and unburned areas
were less than those recorded in 2004
and 2005.
Table 3 provides pre- and post-fire
survey data from the 12 sites. For the 3
unburned sites, the number of
individuals increased by 5.4 percent at
the first site (652 in 2004 to 687 in
2008), decreased by 76.3 percent at the
second site (1,458 in 2004 to 346 in
2008), and decreased by 79.0 percent at
the third site (3,081 in 2005 to 647 in
2008) (Service 2008c, Table 2). For the
4 sites that completely burned, the
number of individuals decreased by
94.9 percent at the first site (3,695 in
2005 to 188 in 2008); 98.1 percent at the
second site (314 in 2005 to 6 in 2008);
98.2 percent at the third site (1,115 in
2005 to 20 in 2008), and 100 percent at
the fourth site (224 in 2005 to 0 in 2008)
(Service 2008c, Table 2).
TABLE 3. CENSUS RESULTS FROM THE 2008 POST-WILDFIRE SURVEYS.
EO Number and
Site Number
Burned or
Unburned
2004/2005
Number of
Individuals
2004 or 2005
2008 Number of
Individuals
2004 or 2005
Percent Area
Burned
Individuals
Percent Change
Unburned
2004
652
687
+5.4
U001–7–3
Part-Burned
2004
1,742
1,134
-34.9
21.3
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N004–1
Part-Burned
2004
541
173
-68.0
unknown
U001–6–1
Unburned
2004
1,458
346
-76.3
0
U001–4–35
Unburned
2005
3,081
647
-79.0
0
U001–4–17
Part-Burned
2005
7,486
772
-89.7
94.6
U001–4–33
Part-Burned
2005
349
31
-91.1
unknown
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TABLE 3. CENSUS RESULTS FROM THE 2008 POST-WILDFIRE SURVEYS.—Continued
EO Number and
Site Number
Burned or
Unburned
2004/2005
Number of
Individuals
2004 or 2005
2008 Number of
Individuals
Individuals
Percent Change
2004 or 2005
Percent Area
Burned
Part-Burned
2005
175
13
-92.6
81.1
U001–NV–1
Burned
2005
3,695
188
-94.9
100
U001–4–12
Burned
2005
314
6
-98.1
100
U001–NV–2
Burned
2005
1,115
20
-98.2
100
U001–4–34
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U001–4–30
Burned
2005
224
0
-100.0
100
During our field surveys at the 5 sites
that were partially burned, we observed
a 34.9 percent to 92.6 percent decrease
between the number of Astragalus
anserinus individuals counted in 2004
or 2005 and the number counted in
2008. The sites that had the most
burned area generally reflected larger
decreases in the number of individual
plants (Table 3) (Service 2008c, Table
2). Extant A. anserinus individuals were
also more frequently associated with
unburned areas in the partially burned
sites. For example, approximately 94.6
percent of the occupied area within site
U001–4–17 was burned during the 2007
wildfire (this site represented the site
with the most individuals counted prior
to the 2007 wildfire (7,486)). We
observed that 562 of the 772 individuals
counted in U001–4–17 in 2008 (68.1
percent) occurred in the 5.4 percent of
the site that did not burn. Prior to the
2007 wildfire, A. anserinus densities
were generally higher within the more
sparsely vegetated areas of occupied
sites. It is likely that the number of
individuals detected within the burned
and unburned areas was influenced by
their pre-wildfire distribution,
particularly since sparsely vegetated
areas were less likely to burn. Because
the density of individuals at any
particular site was not measured at a
fine enough resolution in the 2004,
2005, or 2007 surveys, it is difficult to
conclusively compare pre-2007 wildfire
densities to post wildfire densities.
We also compared the acreage
occupied by Astragalus anserinus
between that recorded during the 2004
and 2005 census efforts and what we
observed in June 2008. The occupied
acreage decreased at each of the 12 sites,
which included both burned and
unburned areas, with a range of 37.9 to
100 percent (Service 2008c, Table 2).
The occupied acreage at the 3 sites that
did not burn decreased 62.1 percent,
60.5 percent, and 77.4 percent (average
= 66.6 percent); the reason for the
decrease is unknown. The occupied
acreage at the 5 partially burned sites
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decreased 37.9 percent, 59.9 percent,
97.3 percent, 86.8 percent, and 99.4
percent (average = 73.3 percent). The
occupied acreage at the 4 sites that
completely burned decreased 90.2
percent, 77.0 percent, 96.0 percent, and
100 percent (average = 90.8 percent)
(Service 2008c, Table 2). Since explicit
data collection protocols were not
established to differentiate between map
points at which an individual was
recorded and map polygons which
indicate an area within which one or
more individuals were recorded, we
considered plants to be within the same
polygon if they were within 33 to 66 ft
(10 to 20 m) of one another. For this
reason, determining fire effects by
comparing the burned, unburned, and
partially burned acreage is not as
accurate as comparing the numbers of
individuals that were actually counted.
Despite the significant declines in the
number of individuals and occupied
acreage detected in the 2008 surveys,
some Astragalus anserinus individuals
did survive the effects of the fire. Plants
can survive wildfires in several ways.
Adult plants can survive, plants may resprout from the base, or plants can reestablish from seed (Brown and Smith
2000, p. 33). Field surveys conducted in
November 2007 (after the 2007 wildfire),
documented that most of the aboveground vegetation had been removed at
several A. anserinus sites. During the
subsequent 2008 field surveys, we
observed that some adult plants that
survived inside burned areas were
attached to large woody roots that likely
survived the wildfire. This suggests that
the A. anserinus individuals that
survived the 2007 wildfire likely resprouted after the wildfire. If A.
anserinus is able to remain dormant
during a growing season, the low plant
numbers we observed in 2008 in
unburned sites may indicate that some
plants were dormant at that time,
although we do not have any
information regarding this capability.
We also compared the number of
Astragalus anserinus seedlings counted
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in 2008 between burned areas and areas
that did not burn. We observed that
seedlings made up 11.4 percent of A.
anserinus plants (76 of 665) in burned
areas, 11.5 percent (23 of 200) in
partially burned areas, and 2.1 percent
(68 of 3,222) in unburned areas (Service
2008a, Table 1). Seedlings can become
re-established from surviving plants,
seed dispersal from off-site plants,
wildfire stimulated seed banks, or
plants that re-sprout after a wildfire
(USFS 2000, p. 33). The increased
number of seedlings within burned and
partially burned areas may demonstrate
that seed germination was stimulated by
the 2007 wildfire. However, even if this
is true, this response did not offset the
observed individual plant losses
resulting from the 2007 wildfire. We are
unaware of any available information on
A. anserinus seed bank longevity, and
do not fully understand the effect
wildfire may have on this species. Seed
bank studies for other Astragalus
species indicate that the group generally
possesses hard impermeable seed coats
with a strong physical germination
barrier. As a result, the seeds are
generally long-lived in the soil and only
a small percentage of seeds germinate
each year (summarized in Morris et al.
2002, p. 30). However, we do not know
if the seed germination strategy for other
Astragalus species is comparable to that
employed by A. anserinus.
We observed an average 50 percent
decline in the number of Astragalus
anserinus plants counted at the 3 sites
that were not burned in the 2007
wildfire, compared to pre-fire site data
for those areas. For sites that were
completely burned by the 2007 wildfire,
average plant numbers declined 97.8
percent from the number of individuals
counted in 2004 or 2005. In some plant
species, seed dormancy is broken by
wildfire (e.g., Pinus contorta, lodgepole
pine), and after a wildfire numerous
seedlings sprout because this seed
dormancy has been broken. However,
we did not see a significant number of
new seedlings within burned areas.
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Because of the low numbers of observed
individuals and the lack of a source for
a large flush of seedlings, it is likely that
A. anserinus recovery will depend on
the successful re-colonization of burned
areas. Because of the generally low
number of seedlings counted, where
data are available, we suspect that this
re-colonization may take several years
and be dependent upon suitable
environmental conditions.
We believe that wildfire frequency
will increase within Astragalus
anserinus habitat. Wildfire return
intervals in the sagebrush-steppe
ecosystem, which includes the Goose
Creek drainage, have been significantly
reduced from between 60 and 110 years
to often less than 5 years. The fact that
the 2007 wildfire was the second
wildfire recorded within a 7–year
period in the Goose Creek drainage,
with no previously recorded wildfires in
this area, appears to present supporting
evidence for increased fire frequency.
Wildfire kills Astragalus anserinus, and
seedling germination does not appear to
be stimulated by wildfire. Accordingly,
increased fire frequency will result in
fewer A. anserinus individuals, and less
seed availability for recruitment. The
ongoing and cumulative effects of
wildfire on A. anserinus include a
substantial reduction in the amount of
available habitat, and range-wide
population-level effects caused by the
loss of approximately 98 percent of the
individual plants in the burned areas
(which were roughly 53 percent of the
pre-2007 wildfire total known
individuals). Future wildfires in the
area will likely result in similar
detrimental effects on the remaining
population.
It is likely that Astragalus anserinus
recovery will depend on the successful
re-colonization of burned areas, which
will probably occur slowly over time.
However, because wildfire frequency
has increased in this area, recovery may
be constrained by additional wildfires
in the relatively near future. Therefore,
we find the magnitude of this threat to
be high.
Wildfire Management
Wildfire management can include
prescribed burning, and activities
associated with fighting wildfires such
as the construction of fire lines and
staging areas, retardant application, and
post-wildfire restoration efforts such as
disking and seeding. In 2008, disking
and seeding associated with soil
stabilization activities occurred over
portions of 11 Astragalus anserinus sites
in Utah in response to the 2007 wildfire
(Service 2008c, Tables 2–4, Map 4;
Service, in litt. 2008, photos 1–3). It is
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likely that numerous individual plants
were lost to site re-seeding efforts and
road construction activities. We also
observed in some cases that A.
anserinus root systems had been
exposed, and believe that it is likely that
individual plants were turned over and
buried during the disking operations.
These actions likely killed individual
plants, thereby compounding the
ongoing detrimental effects of the
wildfire itself on the A. anserinus
population.
impacts to the overall A. anserinus
population. In addition, since advance
A. anserinus surveys were not
conducted because of an immediate
need to respond to the wildfire, we do
not know if the other activities
adversely affected the species. Some fire
fighting activities could present a future
threat to A. anserinus, depending on
their specific location and scale;
however, we are unable to assess the
magnitude of those potential threats at
this time.
Firefighting Activities
Firefighting activities such as
prescribed burning, road and fire line
construction and retardant application
can destroy habitat and kill or injure
individual Astragalus anserinus plants.
Such activities occurred during the
response to the wildfire in 2007.
Advance A. anserinus surveys were not
conducted because of the immediate
need to respond to the 2007 wildfire (M.
Gates, Salt Lake City BLM, in litt.
2008a). During a brief field inspection of
the area affected by firefighting
activities prior to our 2008 post-fire
surveys, we observed that at least one
new road had been constructed along a
ridge, and that several fire lines had
been excavated by hand adjacent to A.
anserinus habitat. We also observed that
a wide fire line had been constructed
between 2 known EOs. During our 2008
post-wildfire surveys over 18 A.
anserinus occupied sites, we observed
that fire retardant had been applied at
1 site over an area approximately 10 ft
(3 m) in radius (U001–4–35). We also
observed that a new access road had
been constructed through site U001–7–
3, and evidence of tire tracks in
occupied areas at site U001–4–33.
One study of the effects of fire
retardant chemical (Phos-Chek G75-F)
and fire suppressant foam (Silv-Ex)
application, alone and in combination
with fire, on Great Basin shrub steppe
vegetation found that growth,
resprouting, flowering, and incidence of
galling insects on Chrysothamnus
viscidiflorus (yellow rabbitbrush) and
Artemisia tridenta (Big sagebrush) were
not affected by any chemical treatment.
In general, the study found that species
richness declined, especially after PhosCheck application, but by the end of the
growing season, species richness did not
differ between treated and control plots
(Larson et al. 1999, p. 115). We are
unaware of the specific retardant used
in the 2007 fire response, or whether A.
anserinus would be similarly
unaffected. However, based on the
limited extent of the area that was
treated with retardant, we do not
anticipate any significant long-term
Post Wildfire Emergency Stabilization
and Restoration
Post-wildfire restoration activities can
also destroy habitat, kill or harm
individuals, and introduce nonnative
species, which may outcompete
Astragalus anserinus for resources. The
following is a discussion of restoration
activities that occurred after the 2008
fires.
2007 Wildfire Emergency
Stabilization and Restoration in Nevada:
Following the 2007 wildfire season, the
BLM Elko Nevada Field Office (BLMNevada) developed a soil stabilization
plan for implementation in 2008 that
included reseeding several areas
affected by the fire. A native grass
restoration seeding effort was planned
near EO 005, but was not conducted
(Howard 2007, p 3). Post-fire aerial
seeding of Artemisia tridentata var.
wyomingensis (Wyoming sagebrush),
which is native to Goose Creek, was
undertaken within drainages at or near
the site instead of the native grass
restoration seeding effort (K. Fuell, Elko
BLM, in litt. 2008, p. 1). This action may
be beneficial to Astragalus anserinus,
however we are unaware of the specific
treatment locations, whether the efforts
were successful, or whether they
affected A. anserinus in EO 005.
2007 Wildfire Emergency
Stabilization and Restoration in Utah:
Restoration seeding activities in Utah
were conducted in late May and early
June, 2008, as part of an Emergency
Stabilization Plan (ESP) that was
developed by BLM to treat areas affected
by the 2007 wildfire. A fencing project
and juniper removal chaining efforts
(using a chain connected between two
tractors) were included as elements of
this plan. Under the ESP, disk seeding
with a mix of native and nonnative
species (see ‘‘Nonnative Invasive
Species—seeded’’ below) was
conducted within Astragalus anserinus
habitat in an area west of Grouse Creek
Road to stabilize the soils, prevent
erosion, and minimize competition by
Bromus tectorum (cheatgrass) in the
burned area. Areas to be avoided were
identified in advance with flagging to
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prevent impacts to A. anserinus from
planned juniper removal chaining
operations and seeding efforts (M. Gates,
in litt. 2008b, p. 1). However, not all A.
anserinus sites were avoided.
The rangeland drills employed in the
Utah seeding effort were fitted with
metal cutting discs measuring at least
1.0 ft (0.30 m) to 1.5 ft (0.46 m) in
diameter, that were spaced on
approximate 8 inch (20 centimeter)
centers. The tractors used in the
restoration activities would generally
pull two rangeland drills at once,
breaking the soil horizon to a depth of
approximately 5 inches (13 centimeters)
and a width of roughly 20 ft (6.1 m)
(Service, in litt. 2008, p. 4, 5). Although
living Astragalus anserinus individuals
were observed between disk furrows
during our site inspections (Service, in
litt. 2008, p. 11–14), we did not observe
any individual plants within the disk
furrows themselves. Our assumption is
that any A. anserinus individuals that
may have been previously established in
these areas were turned over and buried
by the furrowing activities.
The above drilling and seeding
activities were conducted one week
before our 2008 re-census surveys. Since
the work had been recently
accomplished, we were able to observe
evidence of several live Astragalus
anserinus individuals whose woody
roots had been exposed during the
drilling effort. It is unlikely that these
individuals with exposed roots will
survive the physical and physiological
stress of that exposure (Service, in litt.
2008, p. 12, 14). At two sites, the
drilling and seeding efforts affected
clusters of live A. anserinus individuals
that had not been exposed to wildfire
(Service 2008c, Maps 4, 9). During our
2008 surveys, we were unable to
quantify the direct effects of seeding
efforts to A. anserinus for several
reasons: 1) the wildfire reduced plant
numbers such that there were very few
plants left with which to analyze effects,
2) it was difficult to separate the effects
from drilling and seeding from those
associated with the wildfire, and 3)
many of the 2004 and 2005 census
polygons did not completely align with
the areas that were drilled and seeded,
which made comparisons difficult.
Because there were no post-wildfire
project-specific surveys conducted in
advance, it is possible that the remedial
drilling and seeding efforts in Utah
affected previously unknown and
unsurveyed A. anserinus sites.
Although the ESP included plans to
remove dead juniper trees from several
burned areas near Astragalus anserinus
habitat by using a chain connected
between two tractors, we did not
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observe any evidence that this activity
had been conducted during our June
2008 field inspection.
Summary: During our 2008 postwildfire re-census in Utah, we
documented 11 occupied sites within
Utah EO 001 (the largest known
Astragalus anserinus EO) that were
impacted by wildfire management
actions (Service 2008c, Table 3). The 11
affected sites contained an estimated
11,000 individual plants (representing
18 percent of the estimated pre-fire
rangewide population and 34.5 percent
of the pre-fire population numbers
within burned areas). On average, 47.1
percent of the total occupied area of a
site was seeded (Service 2008c, Tables
1, 4), with a range of 13.6 percent to 100
percent of the occupied acreage at each
of the 11 sites affected by disking and
seeding activities (Service 2008c, Table
4). The 11 sites comprised roughly 13
percent (54 of 405 ac (22 of 164 ha)) of
the total area rangewide, with roughly
25 ac (10 ha) or 6 percent of the total
area rangewide being impacted by
disking and seeding activities (Service
2008c, Table 4). It is likely that some A.
anserinus individuals that were
established in these areas were killed
either because of mechanical damage or
burial during the disking operations.
However, we did see live plants
between the furrows that appeared
intact and are likely to survive. Because
4 of the 11 sites were not surveyed in
2004 and 2005 (U001–6–2, U001–6–3,
U001–6–4, and U001–6–New), we do
not have reliable baseline acreage
estimates for these areas. The seeding
efforts conducted under the ESP
affected more than 50 percent of the
occupied acreage at site U001–4–17, the
site with the highest number of
individuals counted in 2005 (7,486
plants). In addition, 117 of the 772
individuals (15.2 percent) counted at
this site in 2008 were within areas
impacted by the seeding activities
(Service 2008c, Tables 3, 4).
We were unable to quantify the direct
effects of remedial seeding activities to
Astragalus anserinus because there were
so few plants left after the 2007 wildfire,
and it was difficult to differentiate the
drilling and seeding effects from the fire
effects. However, it is likely that
numerous individual plants were lost
because of the post-wildfire stabilization
efforts. The effects of wildfire control
activities and seeding efforts were
detrimental to several affected A.
anserinus sites and may continue to be
detrimental because of the overall
reduced recruitment capacity. This
could be exacerbated if future wildfires
result in similar or more aggressive postfire remedial seeding activities in areas
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occupied by A. anserinus, which could
negatively impact the population by
further reducing the number of
individuals. However, the magnitude of
that potential impact could vary widely,
depending on the specific location and
scale of activity and the specific A.
anserinus EO affected. Therefore, we are
unable to assess the magnitude of those
potential threats at this time.
Nonnative Introduced Species—
Unseeded
Invasive nonnative plants (weeds)
invade and alter diverse native
communities, often resulting in
nonnative plant monocultures that
support little wildlife. Many experts
believe that following habitat
destruction, invasive nonnative plants
are the next greatest threat to
biodiversity (Randall 1996, p. 370).
Invasive nonnative plants alter different
ecosystem attributes including
geomorphology, fire regime, hydrology,
microclimate, nutrient cycling, and
productivity (Dukes and Mooney 2004,
p. 4). Invasive nonnative plants can also
detrimentally affect native plants
through competitive exclusion,
alteration of pollinator behaviors, niche
displacement, hybridization, and
changes in insect predation. Examples
are widespread among taxa and
locations or ecosystems (D’Antonio and
Vitousek 1992, pp. 74–75; Olson 1999,
pp. 6–18; Mooney and Cleland 2001, pp.
5446–5451).
Nonnative plants that were not
intentionally seeded and are known to
occur at Astragalus anserinus sites
include Alyssum desertorum (desert
madwort), Bromus tectorum
(cheatgrass), Descurainia sophia
(flixweed), Euphorbia esula (leafy
spurge), and Halogeton glomeratus
(halogeton). In 2008, we also located
one Hyoscyamus niger (black henbane)
individual within one A. anserinus site.
In previous years, this species had only
been observed as a few plants along
Goose Creek road. With regard to the
above nonnative species, the two of
most concern to A. anserinus are B.
tectorum because of possible effect in
altering the wildfire regime (see Wildfire
above), and E. esula because of its
invasive capabilities (DiTomaso 2000, p.
255).
Prior to the 2007 wildfire, Bromus
tectorum was observed throughout the
range of Astragalus anserinus, but was
generally encountered at low density.
Bromus tectorum is documented at all 5
EOs in Idaho, and 3 of the 4 EOs in
Utah. Although habitat information is
available for only 4 of the 10 EOs in
Nevada, B. tectorum is documented at 3.
One Utah EO has not been visited since
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1990, and nonnative species presence
has not been reported (Service 2008b,
17pp.). Bromus tectorum was generally
found at less than 5 percent cover when
it occurred with A. anserinus, based on
estimates from the 2004 and 2005
census efforts. At A. anserinus sites
with either a southern slope exposure or
where livestock trampling was observed
to be more prevalent, the B. tectorum
percent cover was generally higher (e.g.,
between 10 to 20 percent, although as
high as 70 to 80 percent in a few cases)
(Service 2008b, 17 pp.). We do not yet
know how the 2007 wildfire may have
affected B. tectorum abundance, but are
aware that the species often proliferates
as a result of wildfire (D’Antonio and
Vitousek 1992, pp. 74–75). The net
effect of B. tectorum invasion is a
‘‘positive feedback from the initial
colonization in the interstices of shrubs,
followed by fire, to dominance by B.
tectorum and more frequent fire’’
(D’Antonio and Vitousek 1992, pp. 74–
75). However, field observations during
the 2008 re-census effort suggest that B.
tectorum infestations were generally
similar to what they were before the
2007 fire within and outside of areas
burned, although these observations
were not well quantified. This may
imply that B. tectorum may not be a
threat to A. anserinus at this time.
However, wildfire frequency is tightly
linked with annual grass abundance. If
wildfire frequency increases, it is
expected that B. tectorum will also
increase in abundance.
Euphorbia esula (leafy spurge) is a
perennial forb with a deep and
extensive spreading root system, which
can be up to 20 ft (6 m) long. E. esula
also spreads by seeds that are
explosively dispersed as much as 15 ft
(4.5 m). This species has been
designated as a noxious weed by the
state of Idaho, meaning it has the
potential to cause injury to public
health, crops, livestock, land or other
property (Idaho Statute 22–2402). It
reduces species diversity (Selleck et al.
1962, p.21; Butler and Cogan 2004, p.
308), forms almost homogeneous plant
communities (Belcher and Wilson 1989,
p. 174), poses a threat to other rare plant
species such as Platanthera praeclara,
(western prairie fringed orchid) (Kirby
et al. 2003, p. 466), and is known from
42 of the 44 counties in Idaho (Invaders
Database System 2008). It generally
forms monocultures with very little
native vegetation in the areas where it
is found in the Goose Creek drainage.
Euphorbia esula has not been
documented at Astragalus anserinus
sites in Nevada; however, it has been
documented at 4 of 5 A. anserinus EOs
in Idaho and within the largest EO in
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Utah (Service 2008b, 17 pp.). In general,
most E. esula sites are small in size,
dispersed throughout A. anserinus EOs,
and impact only small portions of some
sites. In Utah EO 001, E. esula occurs in
1 of the 54 known occupied sites, and
from 10 to 200 ft (3 to 61 m) away at
6 other sites (Service 2008b, 17 pp.). In
Idaho EO 003, it is present in 13 of the
26 A. anserinus sites, although we have
not established that all of these
exposures directly overlie A. anserinus
sites. It has also been documented as
occurring in the area at seven other sites
in Idaho (Service 2008b, 17 pp.). Based
on field observations in 2004 and 2005,
we estimate that E. esula co-occurs with
A. anserinus at less than 2 percent of the
total range-wide occupied area. In 2008,
we observed two leafy spurge sites that
had been disked and seeded during the
post fire restoration effort in Utah
(Service 2008c, Maps 7, 9; Service, in
litt. 2008, pp. 15–16). This action may
result in a substantial increase in E.
esula, since one study examining the
effects of tilling on E. esula found a
three-fold increase in the number of
stems per square meter after tilling was
conducted (Selleck et al. 1962, p. 14).
Euphorbia esula control efforts within
the Goose Creek drainage have been
underway for several years; from 1999
through 2007, control efforts were
conducted at over 500 sites in Idaho.
Approximately 40 percent of the E.
esula sites documented between 1999
and 2006 at Idaho EO 003 were no
longer present in 2007 as a result of
these efforts (A. Feldhausen, in litt.
2007, pp. 5–6). However, despite a
rather intense control program in Utah,
the species presence is increasing
(Hardy 2005, p. 2). In 2007, increasingly
aggressive control and monitoring
efforts targeting E. esula were expanded
and implemented at several Astragalus
anserinus and Penstemon idahoensis
sites in Utah and Idaho. BLM-Idaho
established 11 small study plots to
determine the effectiveness of E. esula
treatments and to monitor any effects to
A. anserinus and P. idahoensis (A.
Feldhausen, in litt. 2007a, p. 3). Control
efforts have expanded in the Goose
Creek drainage in Idaho and Utah, but
E. esula is still found in or near at least
20 A. anserinus sites in 5 EOs in Idaho
and Utah (Service 2006b, p.4; A.
Feldhausen, in litt. 2007a, p. 3; Service
2008b, 17pp.). In the Nevada portion of
the Goose Creek drainage, BLM-Nevada
has not conducted any invasive species
management activities and none are
planned (Howard 2007, p. 3).
The potential for Euphorbia esula and
Bromus tectorum to become established
throughout the entire Goose Creek
drainage poses a threat to Astragalus
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anserinus. However, infestations of both
species are currently limited and do not
impact all occupied sites. In Idaho,
control efforts appear to have been
effective in eliminating E. esula at some
sites and in controlling its spread. We
recognize that this threat could become
greater in the future, if wildfire
frequency increases such that it
promotes the spread of B. tectorum into
A. anserinus EOs, since B. tectorum is
highly invasive, highly flammable, dies
and dries out in the spring, and spreads
fire rapidly (D’Antonio and Vitousek
1992, p. 74). The magnitude of the
potential threat presented by B.
tectorum or E. esula competition would
vary depending on the location and
scale of the infestations, the specific A.
anserinus EO(s) affected, and the
effectiveness of any control treatments.
As a result, we are unable to assess the
likelihood or magnitude of future
threats at this time.
Nonnative Introduced Species—Seeded
Agropyron cristatum (crested
wheatgrass) was planted in the Goose
Creek drainage before 1970 (Hardy 2005,
p. 2; A. Feldhausen, in litt. 2007, p. 10;
Howard 2007, p. 3). It was planted
extensively near Astragalus anserinus
sites during range seeding operations in
the 1950s and 1960s, and also during
wildfire restoration activities conducted
within the Goose Creek drainage in
2007. Although A. cristatum is by far
the most common intentionally seeded
nonnative species, other nonnative
species have also been introduced,
including Agropyron fragile (Vavilov
Siberian wheatgrass), Elymus junceus
(Russian wildrye), Elymus lanceolatus
ssp. lanceolatus (Critana thickspike
wheatgrass), Linum perenne (Apar
blueflax), Medicago sativa (Ladak
alfalfa), and Thinopyrum ponticum (=
Agropyron elongatum, tall wheatgrass)
(M. Gates, in litt. 2008e, p. 1; R. Hardy,
in litt. 2008, p. 1).
Agropyron cristatum is often used for
rangeland seedings because seed is
widely available, it establishes easily,
provides suitable forage for livestock,
provides some erosion control, and
controls competition from other
invasive nonnative plants (Walker and
Shaw 2001, p.56). A. cristatum is
extremely competitive and can outcompete other vegetation in several
ways (Pellant and Lysne 2005, pp. 82–
83). A. cristatum seedlings are better
than some native species at acquiring
moisture at low temperatures (Lesica
and DeLuca 1998, p. 1; Pyke and Archer
1991, p. 4; Bunting et al. 2003, p. 82),
and A. cristatum plantings are very
stable and may inhibit or retard the
development of a native plant
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community (Marlette and Anderson
1986, p. 173). Range surveys conducted
in 1966 in southern Idaho documented
that A. cristatum had persisted in some
areas for 30 to 50 years and was
spreading into adjacent habitats (Hull
and Klomp 1966, p. 7; 1967, p. 227).
Increasing plant diversity within A.
cristatum sites is challenging, and
requires the implementation of
measures to reduce its ability to
compete before native species can be
introduced (Pellant and Lysne 2005, pp.
84–87).
Prior to 2008, Agropyron cristatum
had been documented at 2 of 5
Astragalus anserinus EOs in Idaho, and
1 of the 4 EOs in Nevada where we had
habitat information. A.gropyron
cristatum has the largest extent of area
in A. anserinus habitat in Utah, where
it was found extensively in the largest
Utah EO (EO 001) (Service 2008b, 17
pp.). Although not quantified, some of
the new EOs found in 2006 in Nevada
were observed to be occupied by A.
cristatum (Howard 2007, p. 3; Smith
2007, p.2). However, where both species
co-occur they are typically separated,
with A. cristatum growing on flatter
areas and A. anserinus on slopes
(Service 2006b, p. 5). Maps obtained
from BLM-Utah indicate that A.
cristatum had been seeded directly over
numerous A. anserinus EOs, although,
based on our field observations during
the 2004 and 2005 census efforts, we
were unable to confirm whether this
actually occurred. A. cristatum was
seldom observed where A. anserinus
occurred, which indicates that the steep
slopes may have been too difficult to
plant and were avoided (Service 2006b,
p. 5). We observed that A. anserinus
density appeared to be higher on flat
areas below tuffaceous outcrops where
A. cristatum was not seeded (Service
2008b, 17 pp.) than on flat areas where
A. cristatum was seeded. Two sites
surveyed in 2005 (U001–NV–1 and
U001–NV–2) were unusual in that we
observed a high density of A. anserinus
individuals in flat areas, as opposed to
sloping areas where they are typically
observed; these areas had not been
seeded with A. cristatum.
Areas disturbed in 2004 during
construction of a livestock watering
pipeline that impacted one Astragalus
anserinus site in Utah (see Livestock Use
below) were reseeded with several
nonnative species, including Agropyron
fragile, Elymus junceus, Elymus
lanceolatus ssp. lanceolatus, Medicago
sativa, and Thinopyrum ponticum (M.
Gates, in litt. 2008e, p. 1). We are
unaware of the effect this activity may
have had on A. anserinus since we have
not inspected the pipeline subsequent to
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its construction. The monitoring
associated with this project was limited
to tracking effects of reseeding on five
A. anserinus individuals in livestock
exclusion cages.
Some areas in Utah that burned
during the 2007 wildfire were reseeded
in 2008 with Achillea millefolium
(western yarrow)—a native forb;
Pascopyrum smithii—a native grass;
canby bluegrass (Poa secunda Canbar)—
a native grass; Agropyron cristatum—a
nonnative grass; Elymus junceus—a
nonnative grass; Linum perenne—a
nonnative forb; and Medicago sativa—a
nonnative forb (M. Gates, in litt. 2008b,
p. 1). Although the intention of these
restoration efforts was to avoid known
occupied A. anserinus habitat (M. Gates,
in litt. 2008b, p. 1), we observed during
our 2008 survey that 11 sites within
Utah EO 001 (the largest EO) had been
drilled and seeded (Service 2008c, Table
3) (see the ‘‘2007 Wildfire Emergency
Stabilization and Rehabilitation in
Utah’’ section above for more details).
We do not fully understand the effects
of the seeding efforts on occupied
Astragalus anserinus areas. The
available literature has documented that
Agropyron cristatum, which is
frequently used to stabilize soils
disturbed by fire, is able to out-compete
slower-developing native species
because of its drought tolerance, fibrous
root system, and good seedling vigor
(USDA 2006, p. 1). The seedings of A.
cristatum that were conducted prior to
2008 were generally separated from A.
anserinus areas, and did not appear to
be spreading significantly from the areas
where the species was planted. Because
of this separation, populations of A.
cristatum established due to the pre2008 seeding activities were not
considered to be a threat to A.
anserinus.
The 2008 seeding activities took place
directly over areas that supported
approximately 10 percent of the prewildfire Astragalus anserinus
individuals, although we are unable to
conclusively determine the ongoing or
cumulative effect of this activity on A.
anserinus because of the short time that
has elapsed. In addition, we are not
aware of any specific studies on the
competitive relationship between A.
cristatum and any other Astragalus
species, although A. cristatum is known
to be an effective competitor with other
aggressive introduced plants during the
establishment period (USDA 2006, p. 1).
Summary: The 2008 Agropyron
cristatum seeding activities occurred
directly over areas that supported 18
percent of the pre-2007 wildfire
Astragalus anserinus rangewide
population numbers. We observed A.
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anserinus density to be higher in areas
where A. cristatum was not seeded
(Service 2008b, 17 pp.). We believe A.
cristatum may be outcompeting A.
anserinus in flat areas where A.
cristatum was seeded directly over A.
anserinus during the 1950s and 1960s.
The available literature has documented
that A. cristatum is highly competitive
with other species (USDA 2006, p. 1).
We believe that the reduced population
level effects that resulted from the 2007
wildfire are being exacerbated by the
ongoing competitive effects of nonnative
seeded plants that were introduced for
rangeland improvement and fire
response activities. After fully
considering each of the above factors,
we find the threat presented by
nonnative invasive species to A.
anserinus to be moderate in magnitude,
because of the likelihood of more
frequent wildfire in the area combined
with the cumulative population-level
effects on recruitment and recovery
from past seeding activities.
Livestock Use (Trampling, Water
Developments, and Habitat
Degradation)
Threats related to livestock use
include the physical effects of trampling
of plants, and the effects from range
improvement projects and livestock
water developments that degrade habitat
and concentrate animals. We are
unaware of any research that has
evaluated the effects of livestock use on
Astragalus anserinus specifically;
however, the effects of livestock on
other plant species is well documented
(Milchunas and Lauenroth, 1993, pp.
327–366; Jones 2000, pp. 155–164). To
our knowledge, the effects of livestock
use on A. anserinus pollinators have not
been investigated. However, one study
of another Great Basin Astragalus
species hypothesized that sheep use and
grazing affected the pollinators for that
species through the destruction of
potential nest sites, destruction of
existing nests and contents, direct
trampling of adult bees, and removal of
food resources (Sugden 1985, p. 309).
Livestock use has occurred within the
Goose Creek drainage for more than 150
years, although it was likely much
greater during the late 1800s (Hardy
2005, p. 1). The Goose Creek drainage
was a stopping area for pioneers
traveling the California National Trail
because of the availability of water,
which increased livestock presence in
the area (Howard 2007, p. 3). However,
without pre-livestock baseline
population information on Astragalus
anserinus, it is difficult to assess the
effects of this activity to the species over
time.
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The presence of livestock trails and
evidence of trampling has been
documented at every Astragalus
anserinus EO (Howard 2007, p. 3; A.
Feldhausen, in litt. 2007a, p. 4; Service
2008b, 17 pp.). In addition, all A.
anserinus sites on public land are
within active livestock grazing
allotments. None of these sites have
been fenced or otherwise excluded from
livestock use, other than some
allotments that were recently closed in
Nevada as a result of the 2007 wildfire
(Bluff Creek, Grouse Creek, and Little
Goose Creek) (B. Fuell, Elko BLM, in
litt. 2008, p. 1). One livestock exclusion
fence that is proposed for construction
east of the 2007 wildfire perimeter in
Utah has not yet been installed;
however, BLM has indicated that they
believe that A. anserinus would be
largely undisturbed by this activity (M.
Gates, in litt. 2008c, p. 1; 2008d, p. 1).
This fence, if installed, would protect A.
anserinus sites from livestock use
within areas burned by the 2007
wildfire.
The intensity of livestock use varies
throughout the Goose Creek drainage,
depending on the terrain, location, and
proximity to water sources. For
example, flat areas (especially those
planted with Agropyron cristatum)
generally receive more livestock use
than the steep tuffaceous outcrops
where A. anserinus normally occurs.
Based on field observations from the
2004 and 2005 census efforts, we
estimate that less than 5 percent of any
particular A. anserinus site is being
used as livestock trails, with the
exception of one site located
approximately 328 ft (100 m) from a
water development. The fact that A.
anserinus individuals have not been
observed within well-used trails
suggests that plants are lost to
trampling. However, the species is
sometimes observed to be abundant
along trail margins. The relatively
sparse vegetation within most occupied
sites and the species’ apparent ability to
tolerate some level of disturbance has
likely helped it persist.
Water tanks, placement of salt licks,
and fence construction may alter
livestock grazing patterns and influence
the effects of trampling at some
Astragalus anserinus sites by
concentrating animals. In general, the
few fences that occur within A.
anserinus habitat occur on private
lands. Although salt licks can increase
livestock use in an area, we are only
aware of one salt lick, which was placed
approximately 330 ft (100 m) from EO
(N004) in Nevada. We are also aware of
two fences within the Goose Creek
drainage in Utah. One was installed
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adjacent to Pole Creek to protect the
creek from livestock (Service 2005a, p.
3), although its effects, if any, to A.
anserinus are unknown. A new fence is
proposed for construction east of the
2007 wildfire perimeter to protect
burned areas from livestock entry but is
not expected to affect A. anserinus (M.
Gates, in litt. 2008c, p. 1; 2008d, p. 1).
We are aware of five livestock water
tanks located within 1 mi (1.6 km) of
Astragalus anserinus sites. The
availability of watering locations can
influence livestock grazing patterns by
concentrating animals in certain areas,
affecting native vegetation. During our
2004 plant census, we observed that an
area extending approximately 150 ft (45
m) around the tanks had been
completely denuded of vegetation from
livestock use. A water pipeline
constructed in Utah in 1987 delivers
water to two livestock tanks sited within
A. anserinus habitat (Hardy 2005, p. 3).
One of the tanks is located within 330
ft (100 m) of an occupied A. anserinus
site. Thirteen A. anserinus plants were
observed immediately outside the
denuded area around this tank, although
we are unaware as to whether the
species was present prior to
construction because this was a recently
discovered site at an existing EO
(Service 2006b, p. 2). A site within this
same EO but approximately 450 ft (140
m) away from the closest water tank was
partially protected from livestock access
because of its location on a steep bluff.
More than 850 A. anserinus individuals
were recorded within this partially
protected EO.
Another livestock watering tank was
constructed in 2004 on an extensive flat
area within Utah EO 003. Although the
nearest Astragalus anserinus
individuals are located approximately
1,600 ft (485 m) from the tank itself
(Service 2006b, p. 3), the pipeline
serving this and another water tank
went through the upper portion of EO
003. Although no A. anserinus plants
were observed in the construction area
during BLM’s 2000 and 2002 site
surveys, plants were subsequently
discovered during a 2004 preconstruction survey. However, no A.
anserinus individuals were lost during
project implementation (Service 2005a,
p. 3). The areas that were disturbed by
construction were seeded with
nonnative forage species (see Nonnative
Invasive Species seeded section), and
monitoring efforts are underway to
detect any changes to A. anserinus. As
part of the pipeline monitoring efforts,
four livestock exclosure cages
measuring approximately 3 ft by 3 ft (0.9
m by 0.9 m) were established.
Vegetation is being monitored to detect
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changes to A. anserinus within and
outside of the cages (Hardy 2005, p. 7;
Service 2005a, p. 3). In addition, BLM
proposes to construct a livestock
exclosure around 1 ac (0.4 ha) of
occupied habitat at this location and
conduct a census of A. anserinus within
and adjacent to the exclosure (Hardy
2005, p. 7).
Another water tank has been in place
for over 15 years between two
Astragalus anserinus EOs on BLM land
in Idaho (EOs 004 and 009), but is
located is at least 3,000 ft (900 m) away
from any known A. anserinus
individuals (Service 2005b, p. 3). An
above-ground pipeline and opening
valve was constructed within EO 004,
but plans are being developed to
relocate the pipeline beneath an existing
unimproved road. This pipeline also
distributes water to several water tanks
on the Sawtooth National Forest, but
those tanks are not within any known A.
anserinus locations. The pipeline
relocation project has not been
accomplished to date (J. Tharp, in litt.
2008b, p. 1), and an environmental
assessment will be completed prior to
implementation to identify and develop
appropriate measures to avoid or
minimize any adverse effects of this
activity to A. anserinus (Service 2005b,
p.3). An additional water tank (the
Delano Well site), is located
approximately 1,200 ft (370 m) from
Nevada EO 002, where 10 individual
plants were counted in 2006 (Howard
2007, p. 2). However, since we don’t
have any pre-construction survey
information, we don’t know whether the
construction of the Delano Well site
affected A. anserinus. We are unaware
of any future plans by BLM to develop
water tanks within A. anserinus habitat.
In addition to direct consumption (see
discussion of herbivory under Factor D
below) and trampling impacts, habitat
degradation and alterations to the
ecosystem associated with livestock use
may also be a concern (Milchunas and
Lauenroth, 1993, pp. 327–366; Jones
2000, pp. 155–164). Jones (2000)
analyzed 54 studies and 16 variables to
assess grazing on North American arid
ecosystems across elevations, from
forest ecosystems to grasslands, and
across different grazing systems. The
author found that 11 of the 16 variables
that were evaluated revealed significant
detrimental effects from cattle grazing
(Jones 2000, p. 159). Some of the
adverse effects from livestock that have
been documented in studies include
changes in the timing and availability of
pollinator food plants (Kearns and
Inouye 1997, pp. 298–299); changes to
insect communities (Kearns and Inouye
1997, pp. 298–299; Debano 2006, pp.
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2553–2554); changes in water
infiltration due to soil compaction
(Jones 2000, Table 1); disturbance to soil
microbiotic crusts (Belnap et al. 1999, p.
167; Jones 2000, Table 1); subsequent
weed invasions (Parker et al. 2006, pp.
1459–1461); and soil erosion from hoof
action (Jones 2000, Table 1). Portions of
at least 1 EO in Idaho, 2 EOs in Nevada,
and the largest EO in Utah (EEO 001)
show evidence of soil microbiotic crusts
that have been trampled by livestock
(Service 2008b, 17 pp). In addition, at
least 1 EO in Idaho, 1 EO in Nevada,
and the largest EO in Utah (EO 001)
exhibit deeply incised washes (Service
2008b, 17 pp.). Given that all EOs on
public lands are within active grazing
allotments, the possibility of such
effects occurring to Astragalus
anserinus is high.
Summary: Livestock use has been
documented at every Astragalus
anserinus EO, and all sites on public
land are within active grazing
allotments. Livestock can trample
plants, however, many of the A.
anserinus sites are on sloping hillsides
that livestock generally avoid. Since A.
anserinus individuals have not been
observed within well-used trails, any
individuals that may have been present
within the trail footprint prior to
livestock use were likely lost to
trampling. The fact that the species is
sometimes abundant along trail margins
suggests it is able to persist at some
lower level of disturbance. Based on
these factors, even though grazing is
ongoing, the magnitude of livestockrelated threats (including fence
construction and water tank
construction) is considered low to
moderate. The magnitude of this threat
could increase in the future if livestock
management activities or new water
developments are implemented in a
manner that concentrates animals
around A. anserinus EOs.
Development (Road Construction and
Maintenance, Utilities, Garbage Dumps,
Private Properties)
In general, the Goose Creek drainage
in Idaho, Utah, and Nevada where
Astragalus anserinus is found is
sparsely populated, and the effects of
development are relatively minor.
Across the range of the species, we
estimate there are fewer than ten
human-inhabited areas (each with fewer
than five buildings). Mancuso and
Moseley (1991, p. 22), indicate that
some A. anserinus habitat was likely
destroyed during the construction of
secondary access roads that cross much
of the Goose Creek drainage. We have
documented roads affecting small
portions of 3 of 5 EOs in Idaho, 1 of the
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4 EOs in Nevada (for which we have
habitat information), and 2 of 4 EOs in
Utah, including the largest EO (EO 001)
(Service 2008b, 17 pp.). In addition,
new roads and fire lines associated with
the 2007 wildfire impacted some sites in
Utah (see Wildfire Management and
Firefighting Activities above). Most of
the land adjacent to Goose Creek is
privately owned, and has been largely
converted to livestock pasture. The
status of A. anserinus on private land is
largely unknown, because most of the
known sites have not been visited since
the early 1990s. Because of the
remoteness of the Goose Creek drainage,
development impacts on A. anserinus
have been few and localized to date.
Most A. anserinus EOs are made up of
several sites within 0.6 mi (1 km) of
each other, so population-level effects
often associated with habitat
fragmentation are not anticipated. In
this regard, we do not anticipate any
significant continuing or cumulative
effects to A. anserinus from the existing
roads or development. Since we are also
unaware of any future development
plans in the area, we consider the
magnitude of this threat to be low.
Recreation (Off-Highway Vehicle Use)
Recent census and survey efforts have
not documented any impacts to
Astragalus anserinus because of
recreational use (Service 2008b, 17 pp.).
Accordingly, we consider this potential
threat to be low in magnitude and non
imminent.
Mining
One expired mineral exploration
permit did overlap with a portion of EO
002 in Nevada (Howard 2007, p. 3), and
another mineral development firm has
expressed interest in exploring areas
south of the Goose Creek drainage near
an existing Astragalus anserinus EO in
Nevada (M. Hemker, Idaho Fish and
Wildlife Office, in litt. 2006). However,
we are unaware of any other mining
efforts that could potentially affect A.
anserinus or its habitat. Based on the
limited mining interest that has been
identified in the Goose Creek vicinity to
date, we consider this threat to be low
in magnitude and non-imminent.
Summary of Factor A
The 2007 wildfire severely
constrained the range and numbers of
the population, significantly reducing
the number of Astragalus anserinus
plants available for recruitment. This
threat is exacerbated by the increased
fire return interval in the sagebrushsteppe ecosystem, which increases the
possibility that another wildfire will
occur before the species can recover
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from the loss of individuals associated
with the 2007 wildfire. Accordingly, we
find the negative rangewide,
population-level effects both from the
2007 wildfire and potential future
wildfires to be high in magnitude.
However, this threat is not considered to
be imminent since we cannot predict
when the next fire may occur.
The threat presented from
competition by seeded and unseeded
nonnative plant species will likely add
to the negative wildfire effects on the
Astragalus anserinus population,
further reducing its ability to recover.
Accordingly, we have determined that
this threat is also moderate in
magnitude. The mechanical damage to
A. anserinus individuals from
construction activities and the disking
and seeding efforts related to wildfire
management activities were also
detrimental to several affected A.
anserinus populations. These effects
may continue to impact the species’
overall recruitment capacity; however,
we find them to be moderate to low in
magnitude and non-imminent because
of their localized impact and the
uncertain timing of future activities of
this nature.
Livestock-related threats could
increase in magnitude if new water
developments or management activities
are implemented that significantly
concentrate animals around Astragalus
anserinus EOs, but we are unaware of
any plans in this regard. Accordingly,
we have determined that livestock use
presents a threat that is low to moderate
in magnitude, but non-imminent. The
threats presented by development,
recreation, and mining use in the Goose
Creek drainage and A. anserinus EOs are
considered low in magnitude and nonimminent because of the limited use of
the area for these types of activities.
Factor B. Overutilization for
Commercial, Recreational, Scientific, or
Educational Purposes
We are not aware of any threats
involving the overutilization or
collection of Astragalus anserinus for
any commercial, recreational, scientific,
or educational purposes at this time.
Factor C. Disease or Predation
During the 2004 and 2005 census
efforts, few Astragalus anserinus plants
exhibited signs of herbivory. Those that
did were observed to be eaten near the
ground (e.g., at a height of 1 inch (2
centimeters)), which indicates that
rabbits may have been responsible (G.
Glenne, Idaho Fish and Wildlife Office,
in litt. 2006). We are unaware of any
herbivory attributable to livestock,
native ungulates, or birds, although in
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2004, numerous green caterpillars and
webs were found on plants at one site
in Idaho (Service 2008b, 17 pp.). In
addition, several plants were observed
withering, particularly after the heavy
rains in May of 2005 (IDCDC 2007a,
p.3), which was attributed to either a
fungus or caterpillar damage.
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Summary of Factor C
With very little herbivory by wildlife
or livestock observed or documented,
predation does not appear to pose a
significant threat to Astragalus
anserinus. We have no reason to suspect
this poses a significant threat to the
species. Accordingly, we find the threat
to the species resulting from herbivory
to be low in magnitude and nonimminent. There is no evidence that
disease, such as fungal damage, poses a
significant threat to the species.
Factor D. Inadequacy of Existing
Regulatory Mechanisms
There are no State regulations in
Idaho, Utah, or Nevada that protect
Astragalus anserinus. All A. anserinus
sites on public land are within active
livestock grazing allotments. The status
of A. anserinus on private land is largely
unknown, because most of the known
sites have not been visited since the
early 1990s. The BLM has promulgated
regulations, policies, and guidelines to
protect sensitive species on Federal
lands, control wildfire and rehabilitate
burned areas, and implement rangeland
assessments, standards, and guidelines
to assess rangeland health. In Idaho, A.
anserinus occurs within four livestock
grazing allotments, although we do not
know the extent to which the standards
or assessments are being met (A.
Feldhausen, in litt. 2007, p.4). Trespass
cattle were removed from one of these
allotments in 2007 as an administrative
matter not related to a resource concern
(A. Feldhausen, in litt. 2007b, p. 1); we
have no information regarding whether
these cattle may have impacted A.
anserinus. In Nevada, A. anserinus
occurs within three livestock grazing
allotments, although none of the
livestock management plans for these
allotments have identified A. anserinus
as a species of concern (Howard 2007,
p. 3). Generally, all allotments require
biannual pasture rotations (Howard
2007, pp. 3–4), but do not specifically
address A. anserinus management. We
do not have any information regarding
the implementation of rangeland
standards or assessments within these
allotments, whether the allotments have
been surveyed for A. anserinus, or
whether these rotations benefit A.
anserinus. In Utah, A. anserinus sites
occur within one allotment (Hardy
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2005, p. 1); the Utah Goose Creek Ranch
was established as a private grazing unit
in 1928 and the Goose Creek Allotment
fence was constructed in 1953.
Livestock use on most key forage
species within this allotment is
generally ‘‘light to moderate’’ but has
been ‘‘heavy to severe’’ in some areas in
some years (especially during drought
years) (Hardy 2005, p. 2). A rangeland
standards assessment was conducted in
the Utah Goose Creek drainage in May
of 1999, and determined the western
portion of Goose Creek to be
‘‘functional,’’ and the central portion to
be ‘‘stable’’ with the hydrological
aspects ‘‘functional’’. However, the
central portion’s biotic integrity was
determined to be ‘‘at risk’’ because of a
lack of vegetative diversity (Hardy 2005,
p. 3). This area was primarily occupied
by Artemisia tridentata ssp.
wyomingensis and Agropyron cristatum,
but lacked forbs and other grasses.
Consequently, the western portion of
the Basin was rated as being in the lateseral stage, but the middle part was
rated as being in the mid-seral stage.
BLM guidelines within Utah require
that areas not be grazed for two growing
seasons after a fire treatment (M. Gates,
in litt. 2008d, p. 1), although we
frequently observed livestock within the
area burned in the 2007 fire during our
2008 surveys in Utah. We have been
advised that BLM-Nevada has closed all
burned areas to livestock use until
further notice (B. Fuell, in litt. 2008, p.
1).
As discussed under Factor A, two
livestock water tank and pipeline
projects in Utah and Idaho were
surveyed by the BLM for Astragalus
anserinus prior to construction. Survey
and monitoring efforts specific to A.
anserinus are discussed above; however
range-wide trend monitoring has not
been conducted. The species special
designation status by the BLM requires
that they follow specific management
guidelines; however, we have no
information regarding whether or how
the guidelines are being implemented.
Summary of Factor D
We do not have information on how
BLM standards and guidelines are being
met within livestock allotments that
contain Astragalus anserinus, nor do we
have any information that allotment
management plans address A.
anserinus. We consider the threat
presented by inadequate regulatory
mechanisms to be moderate to low in
magnitude, but non-imminent, because
the native vegetation at A. anserinus
sites appears to be relatively intact and
it appears the standards and guidelines
are probably protective of the species.
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Factor E. Other Natural or Manmade
Factors Affecting Its Continued
Existence
We have no information concerning
pollinators, genetic diversity, or
germination that is specific to
Astragalus anserinus. As such, we are
unable to determine whether these or
any other presently unknown natural or
manmade factors could potentially
affect the ability of this species to
survive into the foreseeable future. With
regard to climate change, Bromus
tectorum and other C3 grasses (C3 refers
to one of three alternative
photosynthetic pathways) are likely to
thrive as atmospheric carbon dioxide
increases, likely influencing wildfire
frequency (Mayeux et al. 1994, p. 98).
Further, as the climate changes, the
abundance and distribution of native
flora and fauna will also likely change.
While the extent to which climate
change may affect A. anserinus habitat
is not fully understood, those effects
could result in physiological stress or
the loss or alteration of habitat. In
addition, an increased occurrence of
extreme events, such as fire and
drought, could also impact the
remaining populations. Endemic species
with limited ranges and adapted to
localized conditions would be expected
to be more severely impacted by climate
change (Midgley et al. 2002, p. 448) than
those considered habitat generalists.
Because the specific effects of probable
climate change are unknown at this
time, we are not able to predict the
foreseeable magnitude of this potential
threat with confidence.
Since most EOs are comprised of
many sites that are within 0.6 mi (1 km)
of each other, genetic exchange should
still be possible given appropriate
pollination vectors, although the scale at
which it occurs may be reduced because
of a reduced number of individuals. One
exception may be Nevada EO–005,
which was small and isolated to begin
with and burned in 2007. Our 2008 field
inspection observed only two plants, so
the genetic bottleneck effects typically
relevant to small population sizes may
be evident in this EO. However, the
surrounding area has not been
thoroughly searched for additional
plants.
Summary of Factor E
We are unaware of any other natural
or manmade factors affecting the
species’ continued existence that
present a current threat to Astragalus
anserinus. We are unable to predict the
magnitude of the threat presented by
probable climate change to A. anserinus
at this time. We also consider the
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potential genetic bottleneck effects to A.
anserinus to be low in magnitude, since
it may only apply to one EO, which has
not been thoroughly surveyed for the
presence of other individuals.
General Threats Summary
Ongoing threats to remaining
Astragalus anserinus individuals
include future habitat degradation and
modifications to the sagebrush-steppe
ecosystem in which it occurs because of
an altered wildfire regime (i.e., fires are
increasing in frequency, size, and
duration); diminished recruitment
capacity resulting from the 2007
wildfire that eliminated 53 percent of
the known individuals (31,500 of
60,000) and burned 25 percent of the
known occupied habitat (100 ac (41 ha)
of 400 ac (164 ha)); loss of additional
individuals and diminished recruitment
capacity from future wildfires; and
ongoing effects of habitat competition
from both seeded and unseeded
nonnative plant species. Other factors
that may threaten A. anserinus to a
lesser extent include livestock use,
recreation, mining, development, and
the inadequacy of regulatory
mechanisms. Climate change effects to
Goose Creek drainage habitats are
possible, but we are unable to predict
the specific impacts of this change to A.
anserinus at this time.
The continuing effect of the 2007
wildfire to the species’ recruitment
capabilities, and the potential for
similar effects to remaining populations
from future fires present the greatest
threats to Astragalus anserinus at this
time. The fact that our post-fire surveys
documented a 50 percent decline in the
number of known A. anserinus
individuals in areas that did not burn
versus a 98 percent decline in the
number of known individuals in areas
that did burn suggests strongly that fire
may kill A. anserinus. We did not
observe any evidence that A. anserinus
seed dormancy is broken by wildfire
during our field inspections, which
occurs in some other plant species.
Based on the best available information,
the species’ capacity to replace the
number of individuals lost to the 2007
wildfire will likely depend on
recruitment, which we believe occurs
slowly based on the average number of
seedlings that were observed during our
post-wildfire surveys. Given what we
believe to be an increasing fire
frequency, it is possible that recruitment
will not restore these populations before
the next fire event. In addition to the
threats related to increased fire
frequency, wildfires now tend to be
larger and burn more uniformly across
the landscape, leaving fewer unburned
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areas, which affects the post-fire
recovery capacity of native sagebrushsteppe vegetation (Whisenant 1990, p. 4;
Knick and Rotenberry 1997, pp. 287,
297; Brooks et al. 2004, pp. 682–683).
These cascading effects increase the
likelihood that the species will become
endangered within the foreseeable
future throughout all or a significant
portion of its range.
The establishment of Euphorbia esula
and Bromus tectorum throughout the
Goose Creek drainage also represents a
potential but not imminent invasive
competition threat to Astragalus
anserinus. E. esula represents a
potential threat primarily because of its
invasive capabilities and its ability to
displace native plants. B. tectorum
represents an additional threat because
of its ability to alter and shorten the
wildfire return regime. However,
infestations for both species are
currently localized, limited in size, and
do not impact all A. anserinus occupied
sites. Further, E. esula control efforts
have increased in recent years, and B.
tectorum invasion appears to be
primarily confined to southern portions
of the Goose Creek drainage.
Nevertheless, if wildfire frequency is
increasing as suggested by the
occurrence of two wildfire events in the
last 7 years, the threat presented by B.
tectorum expansion would likely
increase in magnitude.
Astragalus anserinus normally occurs
in sparsely-vegetated sites, where it is
able to tolerate the physiological
stresses of living in tuffaceous soils that
are apparently not conducive to
supporting other plant species. The
2008 wildfire response included seeding
Agropyron cristatum directly over areas
that supported approximately 18
percent of the pre-wildfire A. anserinus
individuals. A. cristatum is known to be
an effective competitor with other
aggressive introduced plants (USDA
2006, p. 1), and we presume that it may
be an even more effective competitor
with less aggressive plants. If A.
cristatum plants which are seeded
during fire restoration activities are able
to outcompete A. anserinus, it may
displace the species over time. This
threat could increase in magnitude if
seeding activities are conducted to
respond to future wildfires in A.
anserinus habitat.
Finding
As discussed in the Summary of
Factors section, we determined that any
future threat resulting from the effects of
wildfire would be high in magnitude,
based on the continuing populationlevel effects resulting from the 2007
wildfire on recruitment. That threat
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would be exacerbated by fire fighting
response and restoration activities,
including drilling, disking, and seeding
efforts in burned areas, which could
introduce competitive species as
discussed in Factor A.
The wildfire return interval in the
Goose Creek watershed may now be on
the average of every decade (versus
every 60 to 110 years), based on the two
recent occurrences. However, we
acknowledge the uncertainty associated
with establishing trends based on the
limited data available, particularly since
we have no historical records of wildfire
frequency in the Goose Creek
watershed. Preliminary data suggest that
within the 4 sites that were completely
burned by the 2007 wildfire, Astragalus
anserinus numbers declined 98 percent
from the 2004 and 2005 counts (Service
2008c, Table 2). The primary threats to
the species center on the ongoing and
cumulative effects of the 2007 wildfire
and future wildfires to recruitment
capacity, compounded by competition
from nonnative species. Based on our
analysis of the best available
information, we have no reason to
believe that population trends will
improve, nor that the effects of the
primary threats acting on the species
will be ameliorated in the foreseeable
future.
Climate change projection models are
not reasonably accurate for the localized
range of Astragalus anserinus, and
therefore we cannot reasonably predict
that climate change will pose a threat in
the future. Accordingly, because the
specific effects of climate change are
unknown, we are unable to project with
any certainty whether climate change
may lead to such on the ground effects
as changing wildfire regimes or
increasing size and number of invasive
plant populations, which might impact
A. anserinus.
As required by the Act, we considered
the five potential threat factors to assess
whether Astragalus anserinus is
threatened or endangered throughout all
or a significant portion of its range.
When considering the listing status of
the species, the first step in the analysis
is to determine whether the species is in
danger of extinction throughout all of its
range. If this is the case, then we list the
species in its entirety. For instance, if
the threats to a species are directly
acting on only a portion of its range, but
they are at such a large scale that they
place the entire species in danger of
extinction, we would list the entire
species. If, however, we determine a
species is not endangered throughout its
range, we would then evaluate whether
the species is threatened throughout all
or a significant portion of its range.
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Threats affecting Astragalus anserinus
and its habitat are at a magnitude that
threatens the species throughout all of
its range. We acknowledge there are
uncertainties regarding (1) the postwildfire recovery abilities of the species
over the long-term; (2) the return
interval of future wildfires; (3) the
effects of post-fire restoration seeding
activities in occupied areas; and (4) the
extent of invasive nonnative plant
competition that will occur as a result
of wildfire and post-fire restoration
activities. Based on the best available
information, the threats of greatest
concern to A. anserinus include the
continuing effects to its recruitment
capacity due to: (1) the loss of 98
percent of the known individuals in
areas burned in the 2007 wildfire,
versus the loss of 50 percent of the
known individuals in areas that did not
burn; (2) the potential inability of the
species to recover those losses through
recruitment of new individuals before
the next wildfire occurs; and (3)
competition from nonnative plants.
Decreased genetic exchange may present
a threat to Nevada EO–005, which was
a small and isolated site to begin with
and burned in 2007. However, the
genetic bottleneck effects of small
population size would not be a factor at
this time for the other EOs, since they
are composed of several sites within 0.6
mi (1 km) of each other. Accordingly,
genetic exchange between them should
remain possible provided sufficient
pollination vectors are available.
In summary, we have carefully
assessed the best available scientific and
commercial information available
regarding the past, present, and future
threats faced by Astragalus anserinus in
developing this 12- month finding. We
have reviewed the petition, information
in our files, information supplied to us
by State and Federal agencies, peerreviewed literature, and other
unpublished documents. We evaluated
both the extent of the occupied area that
was burned and the decline in the total
number of individual plants that
resulted from the 2007 wildfire. We also
evaluated the 2008 fire rehabilitation
activities, and the effects of competition
from nonnative plants and other
potential threats. Given the possibility
that wildfire frequency may be
increasing, the species may not have an
opportunity to recover before the next
wildfire event. Accordingly, we find
that listing A. anserinus as threatened or
endangered is warranted. However, as
explained in more detail below, an
immediate proposal of a regulation
implementing this action is precluded
by higher priority listing actions, and
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progress is being made to add or remove
qualified species from the Lists of
Endangered and Threatened Wildlife
and Plants.
We have reviewed the available
information to determine if the existing
and foreseeable threats render the
species at risk of extinction now such
that emergency listing is warranted. We
have determined that an emergency
listing is not warranted for this species
at this time because there are extant
populations in Idaho, Nevada, and Utah,
and we do not believe there are any
potential threats of such great
immediacy, severity, and/or scope that
would threaten all of the known
populations with the imminent risk of
extinction. However, if at any time we
determine that emergency listing of
Astragalus anserinus is warranted, we
will initiate an emergency listing.
The Service adopted guidelines on
September 21, 1983 (48 FR 43098) to
establish a rational system for allocating
available appropriations to the highest
priority species when adding species to
the Lists of Endangered or Threatened
Wildlife and Plants or reclassifying
threatened species to endangered status.
The system places greatest importance
on the immediacy and magnitude of
threats, but also factors in the level of
taxonomic distinctiveness by assigning
priority in descending order to
monotypic genera, full species, and
subspecies (or equivalently, distinct
population segments of vertebrates). The
lower the listing priority number, the
higher the listing priority (that is, a
species with an LPN of 1 would have
the highest listing priority).
As a result of our analysis of the best
available scientific and commercial
information, we have assigned
Astragalus anserinus a Listing Priority
Number of 5, based on our finding that
the threats to the species are high in
magnitude but not imminent.
Approximately 98 percent of the
individual plants that had been
previously documented in the areas
burned by the 2007 wildfire were killed,
based on the lack of adult plants as well
as seedlings in the burned areas. In
addition, it is possible that the fire
return interval is increasing in the
Goose Creek drainage. We believe the
rangewide threat from future wildfires
will exacerbate the ongoing effects to
the population’s recruitment capacity
resulting from the 2007 wildfire and is
high in magnitude. However, this and
other threats to the species are not
imminent. While we conclude that
listing Astragalus anserinus is
warranted, an immediate proposal to list
this species is precluded by other higher
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priority listing, which we address
below.
Preclusion and Expeditious Progress
Preclusion is a function of the listing
priority of a species in relation to the
resources that are available and
competing demands for those resources.
Thus, in any given fiscal year (FY),
multiple factors dictate whether it will
be possible to undertake work on a
proposed listing regulation or whether
promulgation of such a proposal is
warranted but precluded by higherpriority listing actions.
The resources available for listing
actions are determined through the
annual Congressional appropriations
process. The appropriation for the
Listing Program is available to support
work involving the following listing
actions: proposed and final listing rules;
90–day and 12–month findings on
petitions to add species to the Lists of
Endangered and Threatened Wildlife
and Plants (Lists) or to change the status
of a species from threatened to
endangered; annual determinations on
prior ‘‘warranted but precluded’’
petition findings as required under
section 4(b)(3)(C)(i) of the Act; proposed
and final rules designating critical
habitat; and litigation-related,
administrative, and program
management functions (including
preparing and allocating budgets,
responding to Congressional and public
inquiries, and conducting public
outreach regarding listing and critical
habitat). The work involved in
preparing various listing documents can
be extensive and may include, but is not
limited to: gathering and assessing the
best scientific and commercial data
available and conducting analyses used
as the basis for our decisions; writing
and publishing documents; and
obtaining, reviewing, and evaluating
public comments and peer review
comments on proposed rules and
incorporating relevant information into
final rules. The number of listing
actions that we can undertake in a given
year also is influenced by the
complexity of those listing actions; that
is, more complex actions generally are
more costly. For example, during the
past several years, the cost (excluding
publication costs) for preparing a 12–
month finding, without a proposed rule,
has ranged from approximately $11,000
for one species with a restricted range
and involving a relatively
uncomplicated analysis to $305,000 for
another species that is wide-ranging and
involving a complex analysis.
We cannot spend more than is
appropriated for the Listing Program
without violating the Anti-Deficiency
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Act (see 31 U.S.C. 1341(a)(1)(A)). In
addition, in FY 1998 and for each fiscal
year since then, Congress has placed a
statutory cap on funds which may be
expended for the Listing Program, equal
to the amount expressly appropriated
for that purpose in that fiscal year. This
cap was designed to prevent funds
appropriated for other functions under
the Act (for example, recovery funds for
removing species from the Lists), or for
other Service programs, from being used
for Listing Program actions (see House
Report 105-163, 105th Congress, 1st
Session, July 1, 1997).
Recognizing that designation of
critical habitat for species already listed
would consume most of the overall
Listing Program appropriation, Congress
also put a critical habitat subcap in
place in FY 2002 and has retained it
each subsequent year to ensure that
some funds are available for other work
in the Listing Program: ‘‘The critical
habitat designation subcap will ensure
that some funding is available to
address other listing activities’’ (House
Report No. 107 - 103, 107th Congress, 1st
Session, June 19, 2001). In FY 2002 and
each year until FY 2006, the Service has
had to use virtually the entire critical
habitat subcap to address courtmandated designations of critical
habitat, and consequently none of the
critical habitat subcap funds have been
available for other listing activities. In
FY 2007, we were able to use some of
the critical habitat subcap funds to fund
proposed listing determinations for
high-priority candidate species. In FY
2008, while we were unable to use any
of the critical habitat subcap funds to
fund proposed listing determinations,
we did use some of this money to fund
the critical habitat portion of some
proposed listing determinations, so that
the proposed listing determination and
proposed critical habitat designation
could be combined into one rule,
thereby being more efficient in our
work. In FY 2009, we anticipate being
able to do the same.
Thus, through the listing cap, the
critical habitat subcap, and the amount
of funds needed to address courtmandated critical habitat designations,
Congress and the courts have in effect
determined the amount of money
available for other listing activities.
Therefore, the funds in the listing cap,
other than those needed to address
court-mandated critical habitat for
already listed species, set the limits on
our determinations of preclusion and
expeditious progress.
Congress also recognized that the
availability of resources was the key
element in deciding whether, when
making a 12–month petition finding, we
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would prepare and issue a listing
proposal or instead make a ‘‘warranted
but precluded’’ finding for a given
species. The Conference Report
accompanying Public Law 97-304,
which established the current statutory
deadlines and the warranted-butprecluded finding, states (in a
discussion on 90–day petition findings
that by its own terms also covers 12–
month findings) that the deadlines were
‘‘not intended to allow the Secretary to
delay commencing the rulemaking
process for any reason other than that
the existence of pending or imminent
proposals to list species subject to a
greater degree of threat would make
allocation of resources to such a petition
[that is, for a lower-ranking species]
unwise.’’
In FY 2009, expeditious progress is
that amount of work that can be
achieved with $8,808,000, which is the
amount of money that Congress
appropriated for the Listing Program
(that is, the portion of the Listing
Program funding not related to critical
habitat designations for species that are
already listed). Our process is to make
our determinations of preclusion on a
nationwide basis to ensure that the
species most in need of listing will be
addressed first and also because we
allocate our listing budget on a
nationwide basis. The $8,808,000 is
being used to fund work in the
following categories: compliance with
court orders and court-approved
settlement agreements requiring that
petition findings or listing
determinations be completed by a
specific date; section 4 (of the Act)
listing actions with absolute statutory
deadlines; essential litigation-related,
administrative, and listing program
management functions; and highpriority listing actions for some of our
candidate species. The allocations for
each specific listing action are identified
in the Service’s FY 2009 Allocation
Table (part of our administrative
record).
In FY 2007, we had more than 120
species with an LPN of 2, based on our
September 21, 1983, guidance for
assigning an LPN for each candidate
species (48 FR 43098). Using this
guidance, we assign each candidate an
LPN of 1 to 12, depending on the
magnitude of threats (high vs. moderate
to low), immediacy of threats (imminent
or nonimminent), and taxonomic status
of the species (in order of priority:
monotypic genus (a species that is the
sole member of a genus); species; or part
of a species (subspecies, distinct
population segment, or significant
portion of the range)). The lower the
listing priority number, the higher the
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listing priority (that is, a species with an
LPN of 1 would have the highest listing
priority). Because of the large number of
high-priority species, we further ranked
the candidate species with an LPN of 2
by using the following extinction-risk
type criteria: International Union for the
Conservation of Nature and Natural
Resources (IUCN) Red list status/rank,
Heritage rank (provided by
NatureServe), Heritage threat rank
(provided by NatureServe), and species
currently with fewer than 50
individuals, or 4 or fewer populations.
Those species with the highest IUCN
rank (critically endangered), the highest
Heritage rank (G1), the highest Heritage
threat rank (substantial, imminent
threats), and currently with fewer than
50 individuals, or fewer than 4
populations, comprised a list of
approximately 40 candidate species
(‘‘Top 40’’). These 40 candidate species
have had the highest priority to receive
funding to work on a proposed listing
determination. As we work on proposed
and final listing rules for these 40
candidates, we are applying the ranking
criteria to the next group of candidates
with LPN of 2 and 3 to determine the
next set of highest priority candidate
species.
To be more efficient in our listing
process, as we work on proposed rules
for these species in the next several
years, we are preparing multi-species
proposals when appropriate, and these
may include species with lower priority
if they overlap geographically or have
the same threats as a species with an
LPN of 2. In addition, available staff
resources are also a factor in
determining high-priority species
provided with funding. Finally,
proposed rules for reclassification of
threatened species to endangered are
lower priority, since as listed species,
they are already afforded the protection
of the Act and implementing
regulations.
As discussed above, we assigned
Astragalus anserinus an LPN of 5, based
on our finding that the threats to the
species are high in magnitude but not
imminent. Pursuant to the 1983
Guidelines, a ‘‘species’’ facing imminent
high-magnitude threats is assigned an
LPN of 1, 2, or 3 depending on its
taxonomic status. Therefore, work on a
proposed listing determination for A.
anserinus is precluded by work on
higher priority candidate species (i.e.,
species with LPN of 1 through 4); listing
actions with absolute statutory, courtordered, or court-approved deadlines;
and final listing determinations for
those species that were proposed for
listing with funds from FY 2008. This
work includes all the actions listed in
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the tables below under expeditious
progress.
As explained above, a determination
that listing is warranted but precluded
must also demonstrate that expeditious
progress is being made to add or remove
qualified species to and from the Lists
of Endangered and Threatened Wildlife
and Plants. (Although we do not discuss
it in detail here, we are also making
expeditious progress in removing
species from the list under the Recovery
program, which is funded by a separate
line item in the budget of the
Endangered Species Program. As
explained above in our description of
the statutory cap on Listing Program
funds, the Recovery Program funds and
actions supported by them cannot be
considered in determining expeditious
progress made in the Listing Program.)
As with our ‘‘precluded’’ finding,
46539
expeditious progress in adding qualified
species to the Lists is a function of the
resources available and the competing
demands for those funds. Given that
limitation, we find that we are making
progress in FY 2009 in the Listing
Program. This progress included
preparing and publishing the following
determinations:
FY 2009 COMPLETED LISTING ACTIONS
Title
Actions
10/15/2008
90-Day Finding on a Petition To List the Least
Chub
Notice of 90–day Petition Finding, Substantial
73 FR 61007 61015
10/21/2008
Listing 48 Species on Kauai as Endangered and
DesignatingCritical Habitat
Proposed Listing, Endangered; Proposed
Critical Habitat
73 FR 62591 62742
10/24/2008
90-Day Finding on a Petition to List the Sacramento Valley Tiger Beetle as Endangered
Notice of 90–day Petition Finding, Not
substantial
73 FR 63421 63424
10/28/2008
90-Day Finding on a Petition To List the Dusky
Tree Vole (Arborimus longicaudus silvicola) as
Threatened or Endangered
Notice of 90–day Petition Finding, Substantial
73 FR 63919 63926
11/25/2008
12-Month Finding on a Petition To List the Northern Mexican Gartersnake (Thamnophis eques
megalops) as Threatened or Endangered With
Critical Habitat; Proposed Rule
Notice 12 month petition finding, Warranted but precluded
73 FR 71787 71826
12/02/2008
90-Day Finding on a Petition To List the Blacktailed Prairie Dog as Threatened or Endangered
Notice 90–day Petition Finding, Substantial
73 FR 73211 73219
12/05/2008
90-Day Finding on a Petition To List the Sacramento Mountains Checkerspot Butterfly
(Euphydryas anicia cloudcrofti) as Endangered
with Critical Habitat
Notice 90–day Petition Finding, Substantial
73 FR 74123 74129
12/18/2008
90-Day Finding on a Petition to Change the Listing Status of the Canada Lynx
Notice 90–day Petition Finding, Substantial
73 FR 76990 76994
1/06/2009
Partial 90-Day Finding on a Petition To List 475
Species in the Southwestern United States as
Threatened or Endangered With Critical Habitat
Notice 90–day Petition Finding, Not substantial
74 FR 419 427
2/05/2009
Partial 90-Day Finding on a Petition To List 206
Species in the in the Midwest and Western
United States as Threatened or Endangered
With Critical Habitat
Notice 90–day Petition Finding, Not substantial
74 FR 6122 6128
2/10/2009
90-Day Finding on a Petition To List the Wyoming
Pocket Gopher as Threatened or Endangered
With Critical Habitat
Notice 90–day Petition Finding, Substantial
74 FR 6558 6563
3/17/2009
Listing Phyllostegia hispida (No Common Name)
as Endangered Throughout Its Range
Final Listing Endangered
74 FR 11319 11327
3/25/2009
12-Month Finding on a Petition to List the YellowBilled Loon as Threatened or Endangered
Notice 12 month petition finding, Warranted but precluded
74 FR 12931 12968
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12-Month Finding on a Petition to List the San
Francisco Bay-Delta Population of the Longfin
Smelt (Spirinchus thaleichthys) as Endangered
Notice 12 month petition finding, Not warranted
74 FR 16169 16175
4/22/2009
90-Day Finding on a Petition To List the
Tehachapi Slender Salamander (Batrachoseps
stebbinsi) as Threatened or Endangered
Notice 90–day Petition Finding, Substantial
74 FR 18336 18341
5/07/2009
90-Day Finding on a Petition To List the American
Pika as Threatened or Endangered with Critical
Habitat
Notice 90–day Petition Finding, Substantial
74 FR 21301 21310
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FY 2009 COMPLETED LISTING ACTIONS—Continued
Title
Actions
5/19/2009
12-Month Finding on a Petition to List the Coaster
Brook Trout as Endangered
Notice 12–month petition finding, Not warranted
74 FR 23376 23388
6/09/2009
90-Day Finding on a Petition To List Oenothera
acutissima (Narrowleaf Evening-primrose) as
Threatened or Endangered
Notice 90–day Petition Finding, Not substantial
74 FR 27266 27271
6/29 /2009
Proposed Endangered Status for the Georgia
Pigtoe Mussel, Interrupted Rocksnail, and
Rough Hornsnail with Critical Habitat
Proposed Listing, Endangered; Proposed
Critical Habitat
74 FR 31113 31151
7/01/2009
90-Day Finding on a Petition to List the Northern
Leopard Frog (Lithobates [=Rana] pipiens) in
the Western United States as Threatened
Notice 90–day Petition Finding, Substantial
74 FR 31389 31401
7/07/2009
12-Month Finding on a Petition To List a Distinct
Population Segment of the Roundtail Chub (Gila
robusta) in the Lower Colorado River Basin
Notice 12–month petition finding, Warranted but precluded
74 FR 32351 32387
7/08/2009
90-Day Finding on a Petition to List the Coqui
Llanero (Eleutherodactylus juanariveroi) as Endangered
Notice 90–day Petition Finding, Substantial
74 FR 32510 32513
7/08/2009
90-Day Finding on a Petition to List the Susan’s
purse-making caddisfly (Ochrotrichia susanae)
as Threatened or Endangered
Notice 90–day Petition Finding, Substantial
74 FR 32514 32521
7/08/2009
Proposed Endangered Status for Flying Earwig
Hawaiian Damselfly (Megalagrion nesiotes) and
Pacific Hawaiian Damselfly (M. pacificum)
Throughout Their Ranges
Proposed Listing, Endangered
74 FR 32490 32510
7/09/2009
Listing Casey’s June Beetle (Dinacoma caseyi) as
Endangered and Designation of Critical Habitat
Proposed Listing, Endangered; Proposed
Critical Habitat
74 FR 32857 32875
7/22/2009
90-Day Finding on a Petition To List the WhiteSided Jackrabbit (Lepus callotis) as Threatened
or Endangered
Notice 90–day Petition Finding, Substantial
74 FR 36152 36158
8/06/2009
Initiation of Status Review for Mountain Whitefish
(Prosopium williamsoni) in the Big Lost River,
Idaho
Notice of Status Review
74 FR 39268 39269
8/11/2009
90-Day Finding on a Petition To List the Jemez
Mountains
Salamander
(Plethodon
neomexicanus) as Threatened or Endangered
With Critical Habitat
Notice 90–day Petition Finding, Substantial
74 FR 40132 40138
8/19/2009
erowe on DSK5CLS3C1PROD with PROPOSALS-1
Publication Date
12-Month Finding on a Petition To List the Ashy
Storm-Petrel as Threatened or Endangered
Notice 12 month petition finding, Not warranted
74 FR 41832 41860
Our expeditious progress also
included work on listing actions, which
we funded in FY 2009, but have not yet
been completed to date. These actions
are listed below. Actions in the top
section of the table are being conducted
under a deadline set by a court. Actions
in the middle section of the table are
being conducted to meet statutory
timelines, that is, timelines required
under the Act. Actions in the bottom
section of the table are high priority
listing actions. These actions include
work primarily on species with an LPN
of 2, and selection of these species is
partially based on available staff
resources, and when appropriate,
VerDate Nov<24>2008
13:54 Sep 09, 2009
Jkt 217001
include species with a lower priority if
they overlap geographically or have the
same threats as the species with the
high priority. Including these species
together in the same proposed rule
results in considerable savings in time
and funding as compared to preparing
separate proposed rules for each of them
in the future.
ACTIONS FUNDED IN FY 2009 BUT NOT
PO 00000
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Species
Action
Actions Subject to Court Order/
Settlement Agreement
Frm 00029
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FR Pages
ACTIONS FUNDED IN FY 2009 BUT NOT
YET COMPLETED—Continued
Species
Action
Slickspot
peppergrass
Final listing determination
Coastal cutthroat
trout
Final listing determination
Mono basin sagegrouse
12–month petition
finding
Sacramento Mtns.
checkerspot butterfly
12–month petition
finding
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ACTIONS FUNDED IN FY 2009 BUT NOT
YET COMPLETED—Continued
Species
ACTIONS FUNDED IN FY 2009 BUT NOT
YET COMPLETED—Continued
Action
Species
ACTIONS FUNDED IN FY 2009 BUT NOT
YET COMPLETED—Continued
Action
Species
Action
SW Bald eagle population
12–month petition
finding
White-Sided Jackrabbit
12–month petition
finding
Wrights marsh thistle
90–day petition finding
Black-tailed prairie
dog
12–month petition
finding
Jemez Mountains
Salamander
12–month petition
finding
White-bark pine
90–day petition finding
Lynx (include New
Mexico in listing)
12–month petition
finding
12–month petition
finding
Puerto Rico harlequin
90–day petition finding
White-tailed prairie
dog
12–month petition
finding
Desert tortoise –
Sonoran population
12–month petition
finding
90–day petition finding
Fisher – Northern
Rocky Mtns. population
90–day petition finding
American pika
4 subspecies of
Pseudocopaeodes
enunus
Southeastern pop
snowy plover &
wintering pop. of
piping plover
90–day petition finding
42 snail species
(Nevada & Utah)
90–day petition finding
HI yellow-faced bees
90–day petition finding
Berry Cave salamander1
90–day petition finding
206 species (partially completed)
90–day petition finding
Ozark chinquapin1
90–day petition finding
475 Southwestern
species (partially
completed)
90–day petition finding
90–day petition finding
Hermes copper butterfly
90–day petition finding
Thorne’s hairstreak
butterfly
90–day petition finding
Actions with Statutory Deadlines
48 Kauai species
Final listing determination
Black-footed albatross
12–month petition
finding
Smooth-billed ani
Mount Charleston
blue butterfly
12–month petition
finding
Bay Springs salamander1
90–day petition finding
Goose Creek milkvetch
12–month petition
finding
Mojave ground
squirrel1
90–day petition finding
Mojave fringe-toed
lizard1
12–month petition
finding
Gopher tortoise –
eastern population
90–day petition finding
Pygmy rabbit
(rangewide)1
12–month petition
finding
Mojave ground
squirrel
90–day petition finding
Kokanee – Lake
Sammamish population1
12–month petition
finding
Pacific walrus
Delta smelt
(uplisting)
12–month petition
finding
Cactus ferruginous
pygmy owl1
12–month petition
finding
Tucson shovelnosed snake1
12–month petition
finding
Northern leopard
frog
12–month petition
finding
Tehachapi slender
salamander
High Priority Listing Actions3
Proposed listing
Proposed listing
90–day petition finding
17 Maui-Nui candidate species (14
plants, 3 tree
snails) (12 with
LPN = 2, 3 with
LPN = 3, 3 with
LPN = 8)
32 species of snails
and slugs
90–day petition finding
Sand dune lizard
(LPN = 2)
Proposed listing
Calopogon
oklahomensis
90–day petition finding
Proposed listing
Striped newt
90–day petition finding
2 Arizona
springsnails
(Pyrgulopsis
bernadina (LPN =
2), Pyrgulopsis
trivialis (LPN = 2))
American dipper –
Black Hills population
90–day petition finding
12–month petition
finding
Sprague’s pipit
90–day petition finding
12–month petition
finding
Southern hickorynut
90–day petition finding
2 New Mexico
springsnails
(Pyrgulopsis
chupaderae (LPN
= 2), Pyrgulopsis
thermalis (LPN =
11))
Proposed listing
Coqui Llanero
erowe on DSK5CLS3C1PROD with PROPOSALS-1
19 Oahu candidate
species (16 plants,
3 damselflies) (15
with LPN = 2, 3
with LPN = 3, 1
with LPN =9)
Susan’s purse-making caddisfly
12–month petition
finding
90–day petition finding
2 mussels (rayed
bean (LPN = 2),
snuffbox No LPN)
Proposed listing
5 Southwest mussel
species
Chihuahua scarfpea
90–day petition finding
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ACTIONS FUNDED IN FY 2009 BUT NOT processes or achieve economies of scale,
such as by batching related actions
YET COMPLETED—Continued
Species
together. Given our limited budget for
implementing section 4 of the Act, these
actions described above collectively
constitute expeditious progress.
Astragalus anserinus will be added to
the list of candidate species upon
publication of this 12–month finding.
We will continue to monitor the status
of this species as new information
becomes available. This review will
determine if a change in status is
warranted, including the need to make
prompt use of emergency listing
procedures.
We intend that any proposed listing
action for Astragalus anserinus will be
as accurate as possible. Therefore, we
will continue to accept additional
information and comments from all
concerned governmental agencies, the
scientific community, industry, or any
other interested party concerning this
finding.
Action
2 mussels
(sheepnose (LPN
= 2),
spectaclecase
(LPN = 4),)
Proposed listing
Ozark hellbender2
(LPN = 3)
Proposed listing
Altamaha
spinymussel (LPN
= 2)
Proposed listing
5 southeast fish
(rush darter (LPN
= 2), chucky
madtom (LPN =
2), yellowcheek
darter (LPN = 2),
Cumberland darter
(LPN = 5), laurel
dace (LPN = 5))
Proposed listing
8 southeast mussels
(southern
kidneyshell (LPN
= 2), round
ebonyshell (LPN =
2), Alabama
pearlshell (LPN =
2), southern
sandshell (LPN =
5), fuzzy pigtoe
(LPN = 5), Choctaw bean (LPN =
5), narrow pigtoe
(LPN = 11), and
tapered pigtoe
(LPN = 11))
Proposed listing
3 Colorado plants
(Pagosa skyrocket
(Ipomopsis
polyantha) (LPN =
2), Parchute
beardtongue
(Penstemon
debilis) (LPN = 2),
Debeque phacelia
(Phacelia
submutica) (LPN =
8))
Proposed listing
References Cited
A complete list of all references cited
is available on the Internet at https://
www.regulations.govand on request
from the Idaho Fish and Wildlife Office
(see ADDRESSES).
Author
The primary authors of this document
are the staff members of the Idaho Fish
and Wildlife Office
Authority
The authority for this action is the
Endangered Species Act of 1973, as
amended (16 U.S.C. 1531 et seq.).
Dated: August 26, 2009
Daniel M. Ashe
Acting Director, U.S. Fish and Wildlife Service
[FR Doc. E9–21754 Filed 9–9–09; 8:45 am]
BILLING CODE 4310–55–S
DEPARTMENT OF THE INTERIOR
Fish and Wildlife Service
erowe on DSK5CLS3C1PROD with PROPOSALS-1
1 Funds
for listing actions for these species
were provided in previous FYs.
2 We funded a proposed rule for this subspecies with an LPN of 3 ahead of other species with LPN of 2, because the threats to the
species were so imminent and of a high magnitude that we considered emergency listing if
we were unable to fund work on a proposed
listing rule in FY 2008.
3 Funds for these high priority listing actions
were provided in FY 2008 and 2009
We have endeavored to make our
listing actions as efficient and timely as
possible, given the requirements of the
relevant law and regulations, and
constraints relating to workload and
personnel. We are continually
considering ways to streamline
VerDate Nov<24>2008
13:54 Sep 09, 2009
Jkt 217001
50 CFR Part 17
[Docket No. FWS-R2-ES-2009-0060]
[92210-1111-0000-B2]
Endangered and Threatened Wildlife
and Plants; 90-Day Finding on a
Petition to List Cirsium wrightii
(Wright’s marsh thistle) as Threatened
or Endangered with Critical Habitat
AGENCY:
Fish and Wildlife Service,
Interior.
ACTION: Notice of 90–day petition
finding and initiation of a status review.
PO 00000
Frm 00031
Fmt 4702
Sfmt 4702
SUMMARY: We, the U.S. Fish and
Wildlife Service (Service), announce a
90–day finding on a petition to list
Cirsium wrightii (Wright’s marsh thistle)
as threatened or endangered under the
Endangered Species Act of 1973, as
amended, and designate critical habitat.
Following a review of the petition, we
find the petition provides substantial
scientific or commercial information
indicating that listing this species may
be warranted. Therefore, with the
publication of this notice, we are
initiating a status review of the species
to determine if the petitioned action is
warranted. To ensure that the status
review is comprehensive, we request
scientific and commercial data
regarding Cirsium wrightii. At the
conclusion of this review, we will issue
a 12–month finding to determine if the
petitioned action is warranted. We will
make a determination on critical habitat
if and when we initiate a listing action
for this species.
DATES: We made the finding announced
in this document on September 10,
2009. To allow us adequate time to
conduct this review, we request that we
receive information on or before
November 9, 2009.
ADDRESSES: You may submit
information by one of the following
methods:
• Federal eRulemaking Portal: https://
www.regulations.gov. Search for docket
FWS-R2-ES-2009-0060 and then follow
the instructions for submitting
comments.
• U.S. mail or hand-delivery: Public
Comments Processing, Attn: FWS-R2ES-2009-0060; Division of Policy and
Directives Management; U.S. Fish and
Wildlife Service; 4401 N. Fairfax Drive,
Suite 222; Arlington, VA 22203.
We will post all information received
on https://www.regulations.gov. This
generally means that we will post any
personal information you provide us
(see the Information Solicited section
below for more details).
FOR FURTHER INFORMATION CONTACT:
Wally ‘‘J’’ Murphy, Field Supervisor,
New Mexico Ecological Services Office,
2105 Osuna NE, Albuquerque, NM
87113; by telephone (505-346-2525) or
by facsimile (505-346-2542). Persons
who use a telecommunications device
for the deaf (TTD) may call the Federal
Information Relay Service (FIRS) at 800877-8339.
SUPPLEMENTARY INFORMATION:
Request for Information
When we make a finding that a
petition presents substantial
information indicating that listing a
species may be warranted, we are
E:\FR\FM\10SEP1.SGM
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Agencies
[Federal Register Volume 74, Number 174 (Thursday, September 10, 2009)]
[Proposed Rules]
[Pages 46521-46542]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E9-21754]
=======================================================================
-----------------------------------------------------------------------
DEPARTMENT OF THE INTERIOR
Fish and Wildlife Service
50 CFR Part 17
[Docket No. FWS-R1-ES-2009-0006]
[MO 922105 0082-B2]
Endangered and Threatened Wildlife and Plants; 12-Month Finding
on a Petition to List Astragalus anserinus (Goose Creek milkvetch) as
Threatened or Endangered
AGENCY: Fish and Wildlife Service, Interior.
ACTION: Notice of a 12-month petition finding.
-----------------------------------------------------------------------
SUMMARY: We, the U.S. Fish and Wildlife Service (Service), announce our
12-month finding on a petition to list Astragalus anserinus (Goose
Creek milkvetch) as a threatened or endangered species under the
Endangered Species Act of 1973, as amended (Act). After a thorough
review of all available scientific and commercial information, we find
that listing A. anserinus under the Act is warranted. However, listing
is currently precluded by higher priority actions to amend the Lists of
Endangered and Threatened Wildlife and Plants. We have assigned a
listing priority number (LPN) of 5 to this species, because the threats
affecting it have a high magnitude, but are non-imminent. Upon
publication of this 12-month petition finding, A. anserinus will be
added to our candidate species list. We will develop a proposed rule to
list A. anserinus as our priorities allow. Any determinations on
critical habitat will be made during development of the proposed rule.
DATES: The finding announced in this document was made on September 10,
2009.
ADDRESSES: This finding is available on the Internet at https://www.regulations.gov at Docket Number FWS-R1-ES-2009-0006. Supporting
documentation we used to prepare this finding is available for public
inspection, by appointment during normal business hours at the U.S.
Fish and Wildlife Service, Utah Field Office, 2369 West Orton Circle
Suite 50, West Valley City, Utah 84119. Please submit any new
information, materials, comments, or questions concerning this finding
to the above address or via electronic mail (e-mail) at http://www.fw1srbocomments@fws.gov.
FOR FURTHER INFORMATION CONTACT: Larry Crist, Field Supervisor, U.S.
Fish and Wildlife Service, Utah Field Office (see ADDRESSES)); by
telephone at 801-975-3330; or by facsimile at 801-975-3331. If you use
a telecommunications device for the deaf (TDD), call the Federal
Information Relay Service (FIRS) at 800-877-8339.
SUPPLEMENTARY INFORMATION:
Background
Section 4(b)(3)(B) of the Act (16 U.S.C. 1531 et seq.) requires
that, for any petition containing substantial scientific and commercial
information that listing may be warranted, we make a finding within 12
months of the date of receipt of the petition on whether the petitioned
action is: (a) Not warranted, (b) warranted, or (c) warranted, but
immediate proposal of a regulation implementing the petitioned action
is precluded by other pending proposals to determine whether species
are threatened or endangered, and expeditious progress is being made to
add or remove qualified species from
[[Page 46522]]
the Lists of Endangered and Threatened Wildlife and Plants. Section
4(b)(3)(C) of the Act requires that we treat a petition for which the
requested action is found to be warranted but precluded as though
resubmitted on the date of such finding; that is, requiring a
subsequent finding to be made within 12 months. We must publish these
12-month findings in the Federal Register.
Previous Federal Actions
On February 3, 2004, we received a petition dated January 30, 2004,
from Red Willow Research, Inc., and 25 other concerned parties (the
Prairie Falcon Audubon Society Chapter Board, Western Watersheds
Project, Utah Environmental Congress, Sawtooth Group of the Sierra
Club, and 21 private citizens) requesting that we list Astragalus
anserinus as threatened or endangered, emergency list the species, and
designate critical habitat concurrently with the listing (Red Willow
Research Inc, in litt. 2004). We acknowledged the receipt of the
petition in a letter to the petitioners in a letter dated February 19,
2004. In that letter, we advised the petitioners that our initial
review of the petition determined that emergency listing was not
warranted, and that if conditions change we would reevaluate the need
for emergency listing. We informed the petitioner that in light of
resource constraints, we anticipated making our initial finding in
Fiscal Year 2005 as to whether the petition contained substantial
information indicating that the action may be warranted.
On August 16, 2007, we published a notice of 90-day finding (72 FR
46023) that the petition presented substantial scientific or commercial
information indicating that listing A. anserinus may be warranted, and
that we were initiating a status review of the species. For more
information, refer to the 90-day finding that was published in the
Federal Register on August 16, 2007 (72 FR 46023). We received
information from the Bureau of Land Management, Idaho Department of
Fish and Game, Red Willow Research Inc. (the petitioner), and the
Cassia County Weed Control office in response to the 90-day finding.
All information received has been fully considered in this finding.
In accordance with the President's memorandum of April 29, 1994,
Government-to-Government Relations with Native American Tribal
Governments (59 FR 22951), Executive Order 13175, and the Department of
the Interior's manual at 512 DM 2, we readily acknowledge our
responsibility to communicate meaningfully with recognized Federal
Tribes on a government-to-government basis. In accordance with
Secretarial Order 3206 of June 5, 1997 (American Indian Tribal Rights,
Federal-Tribal Trust Responsibilities, and the Endangered Species Act),
we readily acknowledge our responsibilities to work directly with the
Tribes in developing programs for healthy ecosystems, to acknowledge
that Tribal lands are not subject to the same controls as Federal
public lands, to remain sensitive to Indian culture, and to make
information available to Tribes. In fulfilling our trust
responsibilities for government-to-government consultation with Tribes,
we met with the Shoshone Paiute Tribes regarding the process taken to
conduct a 12-month status review of Astragalus anserinus. As an outcome
of our government-to-government consultation, we recognize the strong
cultural significance of A. anserinus to the Shoshone Paiute Tribes and
acknowledge that in this 12-month finding. This notice constitutes the
12-month finding on the January 30, 2004, petition to list A. anserinus
as threatened or endangered.
Species Information
Astragalus anserinus was first collected in 1982 by Duane Atwood
from a location in Box Elder County, Utah, and subsequently described
in 1984 (Atwood et al. 1984, p. 263). The species is known only from
tuffaceous (ashy) soils found near Goose Creek on the Idaho, Nevada,
and Utah border, an area approximately 20 miles (mi)(32.5 kilometers
(km)) long and 4 mi (6.4 km) wide. A. anserinus is a low-growing,
matted, perennial forb (flowering herb) in the pea or legume family
(Fabaceae), with grey hairy leaves, pink-purple flowers, and brownish-
red curved seed pods (Mancuso and Moseley 1991, p. 4). This species is
distinguished from A. calycosus (Torrey's milkvetch), A. purshii
(woollypod milkvetch), and A. newberryi (Newberry's milkvetch), the
three other mat-forming Astragalus species found in the Goose Creek
drainage, primarily by its smaller leaflets and flowers, as well as the
color and shape of the seed pods (Baird and Tuhy 1991, p. 1; Mancuso
and Moseley 1991, pp. 4-5). In our August 16, 2007, 90-day finding (72
FR 46023), we used the common name for the species, ``Goose Creek milk-
vetch.'' Here we use ``Astragalus anserinus'' for accuracy, and ``Goose
Creek milkvetch'' (un-hyphenated) to make the taxonomy more consistent
with today's botanical nomenclature.
Biology, Distribution, and Abundance
Astragalus anserinus typically flowers from late May to early June.
The species is assumed to be insect-pollinated, but the specific
pollinators are unknown (Baird and Tuhy 1991, p. 3). Fruit set begins
in early June with fruits remaining on the plants for several months.
Mechanisms of seed dispersal are also unknown, but may include wind
dispersion of seed pods and insect or bird agents (Baird and Tuhy 1991,
p. 3). Because A. anserinus often grows on slopes and because the seed
pods are found close to the ground below the vegetative portions of the
plant, water or gravity dispersal may also be a dispersal mechanism. In
2004 and 2005, clusters of seedlings were occasionally observed on
abandoned ant hills, which could suggest some ant dispersal. Little
scientific research specific to A. anserinus has been conducted beyond
a basic species description and various survey efforts.
Limited information is available regarding Astragalus anserinus
longevity. In September 2004, the U.S. Bureau of Land Management (BLM)
Field Office in Burley, Idaho (BLM-Idaho), permanently marked 10
seedlings in a wash at the base of a tuffaceous outcrop (soils
comprised of volcanic ash and particulates) at one site (Site 1), 8
seedlings and 7 adults at the base of a slope at a second site (Site
2), and 12 seedlings and 10 adults at a third site (Site 3) (A.
Feldhausen, Burley BLM, in litt. 2007a, pp. 8-9). The results of this
effort are summarized in Table 1 below. In a separate monitoring
effort, BLM-Idaho conducted annual counting of A. anserinus individuals
at two sites (Big Site 1 and Big Site 7) from 2004 to 2007. These
results are depicted in Table 2 below. In combination, these two
studies demonstrate large fluctuations in the number of individuals
between years, with Table 2 reflecting almost a doubling or halving in
magnitude between the numbers of individuals observed in successive
years.
[[Page 46523]]
Table 1. Short-term tracking of Astragalus anserinus individuals (2004-2006) (A. Feldhausen, in litt. 2007a, pp. 8-9).
--------------------------------------------------------------------------------------------------------------------------------------------------------
Site 1 Site 2 Site 3
Year --------------------------------------------------------------------------------------------------------------------
Seedlings Seedlings Adults Seedlings Adults
--------------------------------------------------------------------------------------------------------------------------------------------------------
2004 10 seedlings 8 seedlings 7 adults 12 seedlings 10 adults
--------------------------------------------------------------------------------------------------------------------------------------------------------
2005 4 dead, 2 small 6 dead, 1 small 1 dead, 6 alive 1 stake missing, 5 1 dead, 9 with
seedlings (15 leaves seedling (12 leaves), dead, 6 small adults desiccated leaves
each), 4 small adult 1 young adult (3 with pods) and numerous pods
plants with pods
--------------------------------------------------------------------------------------------------------------------------------------------------------
2006 All 6 remaining plants Of the 7 remaining Of the 6 remaining 7 dead, 3 stakes
swept away by water adult plants, 2 dead stakes: 1 stake missing
in a wash and 5 alive missing, 4 dead, 1
adult
--------------------------------------------------------------------------------------------------------------------------------------------------------
Table 2. Monitoring of Astragalus anserinus at two sites in Idaho (A.
Feldhausen, in litt. 2007a, pp. 8-9; Idaho Conservation Data Center
(IDCDC) 2007a, Element Occurrence (EO) 003).
------------------------------------------------------------------------
Year Big Site 1 Big Site 7
------------------------------------------------------------------------
2004 123 total (2 dead, 138 total (42
73 seedlings, 48 seedlings, 96
adults) adults)
------------------------------------------------------------------------
2005 136 total (8 dead, 67 total (3 dead,
13 seedlings, 115 6 seedlings, 58
adults) adults)
------------------------------------------------------------------------
2006 88 total 135 total
------------------------------------------------------------------------
2007 73 total 69 total
------------------------------------------------------------------------
These wide-ranging fluctuations in the number of Astragalus
anserinus individuals observed suggests that the species is either
short-lived or that adult plants may remain dormant during some growing
seasons. If the species is short-lived, corresponding augmentation of
seedlings to replace lost individuals would be expected; however, this
has not been observed. During spring census efforts, seedlings (defined
as young developing plants having 3 or fewer leaves) made up 1,433 of
the 30,281 individuals that were counted in 2005 (4.7 percent), and 167
of the 4,087 individuals counted in 2008 (4.1 percent) (Service 2008a,
p. 1). The definition of seedlings used for purposes of Table 2 is
different than that used in the 2004, 2005, and 2008 census efforts;
with seedlings in Table 2 being defined by young developing plants with
cotyledons (the first leaves to emerge from the ground) present.
Seedlings made up 59.3 percent of the total individuals at Big Site 1
in 2004, and 9.6 percent of the total individuals in 2005. Seedlings
also made up 30.4 percent of the total individuals at Big Site 2 in
2004, and 8.9 percent of the total individuals in 2005 (J. Tharp,
Burley BLM, in litt., 2008a, p. 1). Although we have no direct
information on A. anserinus seedling germination, it would likely be
more or less abundant depending on the time of year sampled. We expect
spring would be the most likely time to observe A. anserinus seedlings,
like many other plants, and the seedlings could be more numerous in
years when climatic conditions are more amenable to their germination
and establishment. One such climatic factor could be annual
precipitation; the amount and timing of this precipitation over the
course of a year could influence seed germination and seedling
recruitment.
During field surveys, several smaller Astragalus anserinus plants
were partially excavated and observed to be attached to large woody
roots. Parts of some individual plants frequently appeared to be dead,
with only a small green portion remaining. This suggests that
vegetative growth may vary during successive years, and that plant size
may not necessarily correspond to the age of the individual. This also
suggests that some A. anserinus individuals may remain dormant for an
entire growing season. In at least one other species of Astragalus (A.
ampullarioides), adult plants can exhibit dormancy (an inactive state)
during a growing season, and the perennial rootstock allows the plant
to survive dry years (Van Buren and Harper 2003b in Service 2006a, p.
8). However, monitoring studies to determine whether A. anserinus also
has this ability have not been conducted.
Table 2 also demonstrates that fluctuations in the number of
Astragalus anserinus individuals can vary across sites during a given
year. For example, the number of individuals counted at Big Site 1
decreased from 136 to 88 between 2005 and 2006, whereas the number of
individuals counted at Big Site 7 increased from 67 to 135 during the
same time period. However, between 2006 and 2007, the number of
individuals counted at Big Site 1 decreased from 88 to 73 and the
number of individuals counted at Big Site 7 decreased 135 to 69. Since
these sites are approximately 0.5 mi (0.8 km) apart on similar aspects,
this suggests that local weather patterns may not be a predominant
factor influencing plant abundance and annual survival.
Although we acknowledge there are some uncertainties with regard to
longevity, plant dormancy, and the effect of climatic factors on A.
anserinus, the observed population trend has been a decrease in the
number of observed individuals.
Astragalus anserinus is endemic to the Goose Creek drainage in
Cassia County, Idaho; Elko County, Nevada; and Box Elder County, Utah.
The Goose Creek drainage occurs within the Great Basin ecosystem; this
drainage receives an annual rainfall average of less than 12 inches (30
centimeters). Element Occurrences (EOs) are areas where a species was
or is recorded to be present. The known EOs of A. anserinus occur at
elevations ranging between 4,900 to 5,885 feet (ft) (1,494 to 1,790
meters (m)) (Idaho Conservation Data Center (IDCDC) 2007b, p. 2; Smith
2007, Table 1). Most A. anserinus EOs are within an approximate 20-mi
(32-km) long by 4-mi (6.4-km) wide area, oriented in a southwest to
northeasterly direction along Goose Creek. However one A. anserinus EO
has been documented outside of the Goose Creek watershed approximately
2 mi (3.2 km) south of any other EOs. The geographic range of the
species has not been extended from that presented in the 90-day finding
(72 FR 46023; August 16, 2007). Based on new information from surveys
[[Page 46524]]
conducted in Nevada in 2006, during which several new EOs were
discovered, gaps in the range have been filled with the 6 new EOs
extending toward the 1 EO outside of the Goose Creek drainage.
Astragalus anserinus occurs in a variety of habitats, but is
typically associated with dry tuffaceous soils from the Salt Lake
Formation that have a silty to sandy texture (Mancuso and Moseley 1991,
p. 12). In Utah, soil series where A. anserinus has been located
include Bluehill fine sandy loam, Codquin gravelly sandy loam,
Cottonthomas fine sandy loam, and Tomsherry fine sandy loam (Hardy
2005, p. 4). The species has been observed growing on steep or flat
sites, with soil textures ranging from silty to sandy to somewhat
gravelly. These habitats can vary from stable areas with little erosion
to washes or steep slopes where erosion is common. It appears that the
species tolerates, and may proliferate with, some level of disturbance,
based on its occurrence on steep slopes where downhill movement of soil
is common, within eroded washes, and along road margins and edges of
cattle trails. However, individuals have not been observed where
vehicle or livestock travel is frequent or where water flows through
washes on a regular basis.
Astragalus anserinus is generally not found on north-facing slopes,
but is found on most other slope aspects within sparsely vegetated
areas in sagebrush and juniper habitats. The estimated total plant
cover (of all species) at sites where A. anserinus occurs is between 10
and 35 percent (Hardy 2005, p. 4; Smith 2007, p. 2). The dominant
native species within the general surrounding plant community include
Artemisia tridentata ssp. wyomingensis (Wyoming big sagebrush),
Juniperus osteosperma (Utah juniper), Chrysothamnus viscidiflorus
(green or yellow rabbitbrush), Poa secunda (Sandberg's bluegrass), and
Hesperostipa comata (needle and thread grass). A. anserinus is
frequently associated with a suite of native species that reside on the
tuffaceous sand (Baird and Tuhy 1991, pp. 2-3) including: Achnatherum
hymenoides (Indian ricegrass), Chaenactis douglasii (Douglas'
dustymaiden), Cryptantha humilis (roundspike cryptantha), Eriogonum
microthecum (slender buckwheat), Eriogonum ovalifolium (cushion
buckwheat), Ipomopsis congesta (= Gilia congesta; ballhead gilia),
Mentzelia albicaulis (whitestem blazingstar), and Phacelia hastata
(silverleaf phacelia). Several nonnative species also co-occur with A.
anserinus (see Nonnative Introduced Species under Summary of Factors
Affecting the Species Rangewide: Factor A, below). Another Goose Creek
drainage endemic, Penstemon idahoensis (Idaho penstemon), is found near
A. anserinus, but these species are seldom found immediately adjacent
to one another. Other sensitive species in the area include Arabis
falcatoria (= Boechera falcatoria; falcate rockcress), and Potentilla
cottamii (Cottam's cinquefoil) (Franklin 2005, pp. 9-10, 159-160).
The Heritage/Conservation Data Center programs in Idaho, Nevada,
and Utah rank Astragalus anserinus as a G2 species, indicating the
species is ``imperiled throughout its range because of rarity or other
factors that make it vulnerable to extinction,'' and S1 (critically
imperiled) in the three states (IDCDC 2007b, p. 2). Heritage/
Conservation Data rankings do not offer any sort of protection, but are
often used to guide other agencies and entities in designating
sensitive species. The BLM has assigned different status designations
to the species in the three states where it occurs. In Idaho, A.
anserinus is designated as a type 2 species, which reflects a rangewide
or globally imperiled species with a high endangerment status. In Utah,
the species is designated as a sensitive plant species (Fortner 2003 in
Franklin 2005, p. 17), and in Nevada the species is designated as a
special status species (Morefield 2001, p. 1). BLM policy provides that
species which are designated as a ``sensitive species'' shall be
protected as candidate species for listing under the Act (BLM 2001, p.
06C1).
Astragalus anserinus is currently known from 19 EO records (5 in
Idaho, 10 in Nevada, and 4 in Utah) (IDCDC 2007b, p.4; Smith 2007, p.
1; Utah Conservation Data Center (UCDC) in litt. 2007, map; Service
2008b, 17 pp.). The number of currently known EOs (19) differs from the
24 EOs identified in the 90-day finding published on August 16, 2007
(72 FR 46023). Recently published NatureServe guidelines for
designating EOs in Idaho and Utah (IDCDC 2007b, p. 1; R. Fitts, Utah
Conservation Data Center, in litt. 2008, p. 1) state that sites
(occupied points, lines, or polygons) that occur within 0.6 mi (1 km)
of each other are within the same EO. Accordingly, several occupied
sites that were designated as individual EOs in our August 16, 2007,
90-day finding were combined. In addition, six new EOs were discovered
in Nevada as a result of survey efforts in 2006. We developed a naming
convention to help us manage and compare EO data for recently
consolidated sites before and after implementation of the NatureServe
guidelines. For example, the designation U001-4-17 identifies Utah EO
001, which was previously identified as Utah EO 004. The suffix 17
reflects a site number that has been assigned according to the sequence
the site was counted in 2004 or 2005. We use our naming convention as
described, as well as EO number in various places throughout this
finding, depending on the context of the particular site being
referenced.
The majority of Astragalus anserinus sites in Idaho, Utah, and
Nevada occur on Federal lands managed by the BLM (Service 2008, 17
pp.). In 2004 and 2005, we conducted a multiagency census and survey
effort for A. anserinus with the BLM, USFS, and natural resource
agencies from the States of Idaho, Nevada, and Utah. Our objective was
to count (census) known sites, survey additional areas, and document
any new populations. In 2004, we examined 33 sites in 5 EOs in Idaho
(3,467 individuals were counted); 6 sites in 3 EOs in Nevada (2,252
individuals were counted); and 11 sites in 2 EOs in Utah (7,558
individuals were counted) (Service 2008, 17 pp.). In 2005, we examined
5 sites at 1 EO in Nevada (3,074 individuals were counted), and 64
sites in 1 EO in Utah (27,207 individuals were counted) (Service 2008,
17 pp). During the 2004 and 2005 census efforts, 40,858 individual
plants of the estimated 60,000 individual plants range-wide (68
percent) were counted at 119 sites in 12 EOs.
Estimating the total Astragalus anserinus population size is
complicated because of the variability in the species annual abundance,
and the different census and survey methods that have been employed.
For example, plant abundance at one site in Idaho over a 4-year period
varied significantly: 138 plants were counted in 2004; 67 plants in
2005; 135 plants in 2006; and 69 plants in 2007 (Service 2008, 17 pp.).
Census efforts in 2008 at 3 sites that were not affected by a
significant wildfire in 2007 demonstrated a general decrease from plant
counts when compared to the 2004 or 2005 data; 1 site increased by 5.4
percent (652 to 687), 1 site decreased by 76.3 percent (1,458 to 346),
and 1 site decreased by 79.0 percent (3,081 to 647) (Service 2008c,
Table 2). Using the best available data for each A. anserinus site, we
estimate that there were approximately 60,000 individuals distributed
across the three states prior to the 2007 wildfires (Service 2008, 17
pp.). However, we recognize the inherent variability associated with
[[Page 46525]]
estimating population size, because of large fluctuations observed
between successive monitoring years and the differing census and survey
methods that have been employed. Generally, the 2004 and 2005 census
counts yielded higher numbers than had been estimated by previous
surveys (Service 2008, pp. 1-6), however, monitoring efforts have not
occurred regularly enough or over a long enough period to allow us to
statistically analyze population trends.
Based on pre-2007 (pre-wildfire) individual plant count data,
approximately 10 percent of all known Astragalus anserinus individuals
occur in Idaho (5,500 plants), 25 percent occur in Nevada (15,500
plants), and 65 percent occur in Utah (39,000 plants) (Service 2008c,
Table 1). State-specific information on the population status of A.
anserinus is described below.
Idaho
Prior to 2004, seven EOs (which are now combined into four EOs
under the NatureServe guidelines) were monitored by the IDCDC, who
reported the number of Astragalus anserinus individuals at most sites
as estimations. The first A. anserinus EO was documented in 1985 (1
year after the species was described (Atwood et al. 1984, p. 263)), but
systematic or comprehensive surveys were not conducted in Idaho until
1991 (Mancuso and Moseley 1991, p. iii). In 1991, the A. anserinus
population in Idaho was estimated at over 914 individuals (Mancuso and
Moseley 1991, pp. 2, 13-14).
During the 2004 census effort, the four known Astragalus anserinus
EOs in Idaho were revisited and three new sites were located (two sites
were within an existing EO and one new site was considered to be a new
EO). In total, 5,052 A. anserinus individuals were counted, with 2,460
of these individuals observed within the original 4 Idaho EOs (Service
2006b, Table 1). Based on pre-2007 EO revisions, census data from 2004
indicated: (a) stable plant numbers at four EOs; (b) an increase in
plant numbers at one EO (compared to pre-2004 survey numbers); and (c)
an unknown change at two EOs (participants were unable to conduct a
complete census because part of the EOs are on private property)
(Service 2006b, Table 1). However, because of the different survey
methodologies employed before 2004, it is difficult to conclusively
compare survey and census results or estimate long-term population
trends for A. anserinus in Idaho (Service 2006b, Table 1).
In 2007, the IDCDC standardized its methodology for designating
Astragalus anserinus EOs to conform to the above referenced NatureServe
guidelines. Under the new methodology, the four existing EOs and the
three new sites found in 2004 were combined into five EOs (EOs 1, 6 and
7 were deleted and added to EO 3; EO 9 was added as a new EO (IDCDC
2007b, p. 4)). The IDCDC methodology also ranks the health of the EOs
based on a weighted formula made up of three elements: EO size (33
percent); EO condition (based on the abundance of native plants,
introduced plants, and anthropogenic disturbance) (33 percent); and EO
landscape context (based on the degree of habitat fragmentation) (33
percent). Rankings are categorized from A through D, with ``A'' ranked
EOs generally representing higher numbers of individuals and higher
quality habitat, and ``D'' ranked EOs generally representing lower
numbers of individuals and lower quality (or degraded) habitat. Under
this ranking system, the IDCDC assigned an ``A'' ranking to one EO,
``B'' rankings to two EOs, and ``C'' rankings to two EOs (IDCDC 2007b,
p. 4).
Monitoring efforts and results in Idaho that have been used to
inform this status assessment for Astragalus anserinus include: (a) the
collection of plant community data and establishment of photo-points in
2000 and 2001 at 3 sites (Mancuso 2001a, pp. 8-9; Mancuso 2001b, p. 2);
(b) census efforts at all Idaho EOs on public land in 2004 (Service
2008b, 17 pp.); (c) conducting annual census efforts at 2 sites in
Idaho since 2004, as summarized in Table 2 above (A. Feldhausen, in
litt. 2007a, pp. 8-9; IDCDC 2007a, EO 003); (d) the permanent marking
and monitoring of A. anserinus individuals at 3 sites from 2004 to 2006
as summarized in Table 1 (A. Feldhausen, in litt. 2007a, pp. 8-9); and
(e), establishing A. anserinus - Penstemon idahoensis - Euphorbia esula
(leafy spurge) control study plots at 11 sites in 2007 by BLM-Idaho (A.
Feldhausen in. litt. 2007a, p. 3).
Nevada
Astragalus anserinus surveys in Nevada were first conducted in 1991
and 1992, resulting in the documentation of 4 EOs, with an estimated
plant abundance of 827 individuals (Morefield 2001, p. 1). Subsequent
census efforts in 2004 and 2005 failed to locate any new sites until
2006, when 6 new EOs with approximately 11,000 individuals were
discovered. The 6 new EOs represent 18.3 percent of the estimated
range-wide population total of 60,000 individuals (Service 2008b, 17
pp.). There are presently ten known EOs in Nevada, as documented by the
Nevada Natural Heritage Program (NNHP) (Smith 2007, p. 1). Site visits
to 4 EOs were conducted during the 2004 and 2005 census efforts, and
4,930 A. anserinus individuals were counted. However, because of the
different survey methodologies employed prior to 2004, it is difficult
to conclusively compare survey and census results or estimate long-term
population trends for the species in Nevada (Service 2006b, Table 1).
In 2008, we counted individuals at two sites during our post-2007
wildfire assessment study, including EO 001 (which partially burned),
and site 1 of EO 004 (which did not burn). We observed that the number
of individuals in EO 001 decreased by 68 percent, while the number of
individuals in EO 004 increased by 5.4 percent (Service 2008c, Table 2)
(see the discussion under Wildfire below for further details on the
2008 study).
Monitoring efforts and results in Nevada that have been used to
inform this status assessment include census efforts conducted in 2004
and 2005 at four EOs (Service 2008b, 17 pp.), and post-wildfire census
efforts in 2008 at two EOs (one that partially burned, and one that did
not burn) (Service 2008c, Table 2, Map 2).
Utah
There were 9 known Astragalus anserinus EOs in Utah with an
estimated 7,617 individuals, based on the results of initial surveys
conducted in 1990 and 1991 (Baird and Tuhy 1991, p. 2; Morefield 2001,
p. 1). Eight of these EOs were documented by the UCDC, and one EO was
documented in the Nevada Natural Heritage Program database, although it
was not reflected in the UCDC database (Mancuso and Moseley 1991, p.2).
There were additional Utah surveys in 1993 (Hardy 2005, p. 4), however
we do not know whether they were resurveys of known sites and do not
believe the results are included in the UCDC database. The BLM Salt
Lake City, Utah field office (BLM-Utah) staff indicates that they are
aware of data from at least one additional site that has not been
submitted to the UCDC (Hardy 2005, p. 4). In addition, surveys were
conducted in Utah by BLM in 2000, 2001, and 2004 to evaluate the
environmental effects of a waterline and livestock water tank
construction project to the species (Hardy 2005, p. 5); no sensitive
plants were discovered along the proposed water line.
Site visits conducted to what was then 6 known EOs, and 1 new site
during 2004 and 2005 census efforts recorded a total of 33,476
Astragalus
[[Page 46526]]
anserinus individuals, although only partial plant counts were
conducted at 3 of the 6 known EOs. Two other documented EOs that had
the greatest numbers of individuals weren't counted during the 2004 and
2005 census efforts because of limitations on access and time
constraints (Service 2006b, Table 1). The 2004 and 2005 census data
indicated higher A. anserinus count numbers than the previous estimates
at five of the known EOs. However, because of the different survey
methodologies that were used before 2004, we are unable to conclusively
compare survey and census results or estimate long-term population
trends for the species in Utah (Service 2006b, Table 1).
In early 2007, the UCDC reconfigured Astragalus anserinus EOs in
Utah to conform to the general EO standards guidebook, IDCDC
methodology, and NatureServe guidelines, resulting in the combining of
the nine previously documented EOs into four EOs (R. Fitts, in litt.
2008). Based on 2005 census estimates, the largest Utah EO (EO 001)
supported over 37,000 plants, making up over 60 percent the known
individuals range-wide (Service 2008b, 17 pp.).
In 2008, re-census efforts were conducted as part of a post-
wildfire assessment at ten sites in Utah where we had information on
the number of individuals from 2004 or 2005 surveys. We surveyed two
sites that did not burn, four sites that were partially burned, and
four sites that were completely burned. At the 2 sites that did not
burn, the individual numbers of plants decreased by 76.3 percent and 79
percent. At the 4 sites that partially burned, the individual numbers
of plants decreased by 34.9 percent, 89.7 percent, 91.1 percent, and
92.6 percent. The individual plant counts at the 4 sites that
completely burned decreased by 94.9 percent, 98.1 percent, 98.2
percent, and 100 percent (Service 2008c, Table 2) (see the Wildfire
discussion under factor A, below, for further information on the 2008
post-wildfire assessment efforts).
Monitoring efforts and results in Utah that have been used to
inform this status assessment include: (a) census efforts conducted in
2004 and 2005 at portions of 2 EOs (Service 2008b, 17 pp.); (b)
installation of 4 small chicken-wire exclosure cages over 5 individual
plants in 2004 to monitor effects of a waterline construction project
(all individuals were still present in 2007) (Hardy 2008, pp. 1-2); (c)
documentation of 2 individual plants within a 300-foot long belt
transect in 2006 (scheduled to be resurveyed in 2010 (Hardy 2008, p.
2)); (d) establishing a study plot in 2007 near a waterline constructed
in 2004 that includes 231 A. anserinus individuals, which may be fenced
in the future (Hardy 2008, p. 1); and (e) conducting field
inspectionsat 10 sites during the 2008 post-wildfire re-census effort
(Service 2008c, Table 2, Map 2).
Summary of Factors Affecting the Species Rangewide
Section 4 of the Act (16 U.S.C. 1533) and implementing regulations
at 50 CFR 424, set forth procedures for adding species to the Federal
Lists of Endangered and Threatened Wildlife and Plants. Under section
(4) of the Act, we may determine a species to be endangered or
threatened based on any of the following five factors: (A) The present
or threatened destruction, modification, or curtailment of habitat or
range; (B) overutilization for commercial, recreation, scientific, or
educational purposes; (C) disease or predation; (D) the inadequacy of
existing regulatory mechanisms; or (E) other natural or manmade factors
affecting its continued existence. In making this finding on a petition
to list Astragalus anserinus, information regarding the status of, and
threats to, A. anserinus in relation to the five factors provided in
section 4(a)(1) of the Act is discussed below.
Factor A. The Present or Threatened Destruction, Modification, or
Curtailment of Its Habitat or Range
Wildfire
Organisms adapt to disturbances such as historical wildfire regimes
(fire frequency, intensity, and seasonality) with which they have
evolved (Landres et al. 1999, p. 1180), and different rare species
respond differently to wildfire (Hessl and Spackman 1995, pp. 1-90). In
general, fire regimes within forest and steppe habitats in the western
United States have been highly disrupted from historical patterns
(Whisenant 1990, pp. 4-10; D'Antonio and Vitousek 1992, pp. 63-87;
Weddell 2001, pp. 1-24). In some instances, fire suppression has
allowed grasslands to be invaded by trees (Burkhardt and Tisdale 1976,
pp. 472-484; Lesica and Martin 2003, p. 516), and in many grassland and
shrub habitats, fire frequencies have increased due to the expansion
and invasion of annual nonnative grasses (Whisenant 1990, pp. 4-10;
D'Antonio and Vitousek 1992, pp. 63-87; Hilty et al. 2004, pp. 89-96).
These invasive annual nonnative grasses become established in
unvegetated areas that would normally separate native vegetation,
dramatically increasing the ability of wildfire to spread.
Our understanding of the historical wildfire regime in the Goose
Creek drainage, and specifically within Astragalus anserinus habitat,
is limited. In general, the average wildfire return interval within the
sagebrush-steppe ecosystem as a whole has been reduced from between 60
and 110 years, to often less than 5 years (Whisenant 1990, p. 4; Wright
and Bailey 1982, p. 158; Billings 1990, pp. 307-308; USGS 1999, pp. 1-
9; West and Young 2000, p. 262). Recent wildfires often tend to be
larger and burn more uniformly across the landscape, leaving fewer
unburned areas, which can affect the post-fire recovery of native
sagebrush-steppe vegetation (Whisenant 1990, p. 4; Knick and Rotenberry
1997, pp. 287, 297; Brooks et al. 2004, pp. 682-683). The result of
this altered wildfire regime has been the conversion of vast areas of
sagebrush-steppe ecosystem into nonnative annual grasslands (USGS 1999,
pp. 1-9). The proportion of annuals in the sagebrush-steppe ecosystem
increases dramatically at higher fire frequencies, while all other
vegetative life forms decrease. Sagebrush can reestablish from seed
following fire, however the seeds are short-lived and if a second fire
occurs before the new plants produce seed (4 to 6 years), the species
may face local extirpation. This would be less of a problem if the
fires occurred over relatively small areas, because seed from adjacent
unburned areas would be naturally transported back into burned areas.
As fires become larger, the opportunity for seed migration into burned
areas is dramatically decreased (Whisenant 1990, p. 8-9). Based on our
observations, Astragalus anserinus seedling germination does not appear
to be stimulated by wildfire. Accordingly, fewer individuals and fewer
seeds would be available for recruitment if wildfire were to return
before the species is able to recover from earlier wildfire impacts to
the population. As a result, there would be a corresponding decline in
the overall number of individuals.
Wildfire was not documented within Astragalus anserinus habitat
prior to 2000 (A. Feldhausen, in litt. 2007, p. 3; R. Hardy, Salt Lake
City BLM, in litt. 2008, p. 1), although undoubtedly they occasionally
occurred in the past. Astragalus anserinus habitat is normally sparsely
vegetated (e.g., typically 10 to 30 percent total vegetative cover),
which likely makes it less vulnerable to wildfire because of the lack
of fuels to sustain fire over large areas. We are aware of a wildfire
that occurred in A.
[[Page 46527]]
anserinus habitat in Idaho in 2000, and another wildfire that occurred
in Nevada and Utah in 2007. The 2000 Idaho wildfire affected two EOs
(EO 007 and EO 009), however at the time, EO 009 had not been
documented and A. anserinus was not affected by the 2000 wildfire at EO
007 (A. Feldhausen, in litt. 2007a, p. 11). Accordingly, before 2008,
we had no pre-wildfire data with which to assess the impact of
wildfires on A. anserinus. Our knowledge of the effects from wildfire
was limited to observations at EO 009 from 2004. Based on the best
available information, EO 009 is made up of 3 separate occupied sites
that contain 10, 36, and 749 individuals based on 2004 surveys/census
efforts. The EO 009 site with 749 individuals is within a sparsely
vegetated slope with mature junipers and shrubs, and may not have
burned during the 2000 wildfire.
Based on pre-fire data, a single wildlfire in 2007 in Nevada and
Utah completely burned 3 EOs and portions of 5 other EOs containing
approximately 53 percent of all known Astragalus anserinus individuals
(31,500 of 60,000 individuals). The 2007 wildfire also burned 25
percent of the known occupied habitat (100 acres (ac) (41 hectares
(ha)) out of an estimated 400 ac (164 ha)) (Service 2008c, Table 1).
In Nevada, 3 EOs were completely within the burned area footprint
(1,512 total individuals), and three other EOs were partially burned,
but had an estimated loss of approximately 72 percent of the
individuals within those 3 EOs (5,394 of 7,508 individuals). In Utah,
portions of two EOs were burned in the wildfire (EOs 001 and 009). The
wildfire in EO 001, which contained more than 60 percent of the known
individuals (37,000 of 60,000 individuals), was estimated to have
burned approximately 40 percent of the known individuals (24,000), and
approximately 18 percent of the total occupied acreage (71 ac (29 ha))
(Service 2008b, 17 pp.). Please note that since six of the 10 currently
known EOs in Nevada were not discovered until 2006 (EOs 005 through
010), and only population estimates and point data have been collected,
the total number of individuals and the acreage affected by the 2007
wildfire are only estimates. Estimating the number of individuals and
acres with greater precision is difficult because of the various
methods that have been employed by prior survey and census efforts.
Based on initial field visits and reports following the 2007
wildfire (Howard 2007, pp. 1-2), we initially understood that the
wildfire burned intensely and almost continuously across the landscape.
However, our 2008 field inspection determined that the wildfire burned
as a mosaic rather than continuously, and did not affect some small
patches of Astragalus anserinus occupied habitat. We observed that 21.3
percent, 81.1 percent, and 94.6 percent of the total acreage was burned
at 3 A. anserinus sites, however estimates were not made for 2 other
sites within the burned area perimeter that were only partially burned
(Service 2008c, Table 2). Our inspection also documented the
bunchgrasses Hesperostipa comata (needle and thread), Poa secunda
(Sandberg's bluegrass), Pascopyron smithii (western wheatgrass),
Agropyron cristatum (crested wheatgrass), and Achnatherum hymenoides
(Indian ricegrass), as well as the shrub Chrysothamnus viscidiflorus
(green or yellow rabbitbrush) re-sprouting from roots that survived the
2007 wildfire. These species generally made up approximately 20 percent
of the total vegetative cover at the burned sites, and it was estimated
that 75 to 90 percent of the bunchgrasses had survived the wildfire (M.
Mancuso, Mancuso Botanical Services, in litt. 2008, p. 1).
In June, 2008, we conducted post-wildfire re-census efforts to
specifically evaluate the effects of the 2007 wildfire and determine
the response of Astragalus anserinus to this event. We counted
individual plants at 12 sites where we had count data from either 2004
or 2005, including Nevada EO 001, Nevada EO 004, and 10 sites within
Utah EO 001 (which represents the largest EO). Three of the sites that
were surveyed were not burned, 5 of the sites were partially burned
(including Utah EO 001-4-17 which supported 7,486 individuals prior to
the fire based on 2005 data), and 4 of the sites were completely
burned. Using pre-2007 information, we estimate that we resurveyed
habitat containing approximately half of the estimated 31,500
individuals burned in the 2007 wildfire (Service 2008c, Tables 1 and
2). Generally, individual plant counts in almost all burned and
unburned areas were less than those recorded in 2004 and 2005.
Table 3 provides pre- and post-fire survey data from the 12 sites.
For the 3 unburned sites, the number of individuals increased by 5.4
percent at the first site (652 in 2004 to 687 in 2008), decreased by
76.3 percent at the second site (1,458 in 2004 to 346 in 2008), and
decreased by 79.0 percent at the third site (3,081 in 2005 to 647 in
2008) (Service 2008c, Table 2). For the 4 sites that completely burned,
the number of individuals decreased by 94.9 percent at the first site
(3,695 in 2005 to 188 in 2008); 98.1 percent at the second site (314 in
2005 to 6 in 2008); 98.2 percent at the third site (1,115 in 2005 to 20
in 2008), and 100 percent at the fourth site (224 in 2005 to 0 in 2008)
(Service 2008c, Table 2).
Table 3. Census results from the 2008 post-wildfire surveys.
--------------------------------------------------------------------------------------------------------------------------------------------------------
2004 or 2005
EO Number and Site Number Burned or Unburned 2004 or 2005 2004/2005 Number 2008 Number of Individuals Percent Area
of Individuals Individuals Percent Change Burned
--------------------------------------------------------------------------------------------------------------------------------------------------------
N004-1 Unburned 2004 652 687 +5.4 ..................
--------------------------------------------------------------------------------------------------------------------------------------------------------
U001-7-3 Part-Burned 2004 1,742 1,134 -34.9 21.3
--------------------------------------------------------------------------------------------------------------------------------------------------------
N001-1 Part-Burned 2004 541 173 -68.0 unknown
--------------------------------------------------------------------------------------------------------------------------------------------------------
U001-6-1 Unburned 2004 1,458 346 -76.3 0
--------------------------------------------------------------------------------------------------------------------------------------------------------
U001-4-35 Unburned 2005 3,081 647 -79.0 0
--------------------------------------------------------------------------------------------------------------------------------------------------------
U001-4-17 Part-Burned 2005 7,486 772 -89.7 94.6
--------------------------------------------------------------------------------------------------------------------------------------------------------
U001-4-33 Part-Burned 2005 349 31 -91.1 unknown
--------------------------------------------------------------------------------------------------------------------------------------------------------
[[Page 46528]]
U001-4-30 Part-Burned 2005 175 13 -92.6 81.1
--------------------------------------------------------------------------------------------------------------------------------------------------------
U001-NV-1 Burned 2005 3,695 188 -94.9 100
--------------------------------------------------------------------------------------------------------------------------------------------------------
U001-4-12 Burned 2005 314 6 -98.1 100
--------------------------------------------------------------------------------------------------------------------------------------------------------
U001-NV-2 Burned 2005 1,115 20 -98.2 100
--------------------------------------------------------------------------------------------------------------------------------------------------------
U001-4-34 Burned 2005 224 0 -100.0 100
--------------------------------------------------------------------------------------------------------------------------------------------------------
During our field surveys at the 5 sites that were partially burned,
we observed a 34.9 percent to 92.6 percent decrease between the number
of Astragalus anserinus individuals counted in 2004 or 2005 and the
number counted in 2008. The sites that had the most burned area
generally reflected larger decreases in the number of individual plants
(Table 3) (Service 2008c, Table 2). Extant A. anserinus individuals
were also more frequently associated with unburned areas in the
partially burned sites. For example, approximately 94.6 percent of the
occupied area within site U001-4-17 was burned during the 2007 wildfire
(this site represented the site with the most individuals counted prior
to the 2007 wildfire (7,486)). We observed that 562 of the 772
individuals counted in U001-4-17 in 2008 (68.1 percent) occurred in the
5.4 percent of the site that did not burn. Prior to the 2007 wildfire,
A. anserinus densities were generally higher within the more sparsely
vegetated areas of occupied sites. It is likely that the number of
individuals detected within the burned and unburned areas was
influenced by their pre-wildfire distribution, particularly since
sparsely vegetated areas were less likely to burn. Because the density
of individuals at any particular site was not measured at a fine enough
resolution in the 2004, 2005, or 2007 surveys, it is difficult to
conclusively compare pre-2007 wildfire densities to post wildfire
densities.
We also compared the acreage occupied by Astragalus anserinus
between that recorded during the 2004 and 2005 census efforts and what
we observed in June 2008. The occupied acreage decreased at each of the
12 sites, which included both burned and unburned areas, with a range
of 37.9 to 100 percent (Service 2008c, Table 2). The occupied acreage
at the 3 sites that did not burn decreased 62.1 percent, 60.5 percent,
and 77.4 percent (average = 66.6 percent); the reason for the decrease
is unknown. The occupied acreage at the 5 partially burned sites
decreased 37.9 percent, 59.9 percent, 97.3 percent, 86.8 percent, and
99.4 percent (average = 73.3 percent). The occupied acreage at the 4
sites that completely burned decreased 90.2 percent, 77.0 percent, 96.0
percent, and 100 percent (average = 90.8 percent) (Service 2008c, Table
2). Since explicit data collection protocols were not established to
differentiate between map points at which an individual was recorded
and map polygons which indicate an area within which one or more
individuals were recorded, we considered plants to be within the same
polygon if they were within 33 to 66 ft (10 to 20 m) of one another.
For this reason, determining fire effects by comparing the burned,
unburned, and partially burned acreage is not as accurate as comparing
the numbers of individuals that were actually counted.
Despite the significant declines in the number of individuals and
occupied acreage detected in the 2008 surveys, some Astragalus
anserinus individuals did survive the effects of the fire. Plants can
survive wildfires in several ways. Adult plants can survive, plants may
re-sprout from the base, or plants can re-establish from seed (Brown
and Smith 2000, p. 33). Field surveys conducted in November 2007 (after
the 2007 wildfire), documented that most of the above-ground vegetation
had been removed at several A. anserinus sites. During the subsequent
2008 field surveys, we observed that some adult plants that survived
inside burned areas were attached to large woody roots that likely
survived the wildfire. This suggests that the A. anserinus individuals
that survived the 2007 wildfire likely re-sprouted after the wildfire.
If A. anserinus is able to remain dormant during a growing season, the
low plant numbers we observed in 2008 in unburned sites may indicate
that some plants were dormant at that time, although we do not have any
information regarding this capability.
We also compared the number of Astragalus anserinus seedlings
counted in 2008 between burned areas and areas that did not burn. We
observed that seedlings made up 11.4 percent of A. anserinus plants (76
of 665) in burned areas, 11.5 percent (23 of 200) in partially burned
areas, and 2.1 percent (68 of 3,222) in unburned areas (Service 2008a,
Table 1). Seedlings can become re-established from surviving plants,
seed dispersal from off-site plants, wildfire stimulated seed banks, or
plants that re-sprout after a wildfire (USFS 2000, p. 33). The
increased number of seedlings within burned and partially burned areas
may demonstrate that seed germination was stimulated by the 2007
wildfire. However, even if this is true, this response did not offset
the observed individual plant losses resulting from the 2007 wildfire.
We are unaware of any available information on A. anserinus seed bank
longevity, and do not fully understand the effect wildfire may have on
this species. Seed bank studies for other Astragalus species indicate
that the group generally possesses hard impermeable seed coats with a
strong physical germination barrier. As a result, the seeds are
generally long-lived in the soil and only a small percentage of seeds
germinate each year (summarized in Morris et al. 2002, p. 30). However,
we do not know if the seed germination strategy for other Astragalus
species is comparable to that employed by A. anserinus.
We observed an average 50 percent decline in the number of
Astragalus anserinus plants counted at the 3 sites that were not burned
in the 2007 wildfire, compared to pre-fire site data for those areas.
For sites that were completely burned by the 2007 wildfire, average
plant numbers declined 97.8 percent from the number of individuals
counted in 2004 or 2005. In some plant species, seed dormancy is broken
by wildfire (e.g., Pinus contorta, lodgepole pine), and after a
wildfire numerous seedlings sprout because this seed dormancy has been
broken. However, we did not see a significant number of new seedlings
within burned areas.
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Because of the low numbers of observed individuals and the lack of a
source for a large flush of seedlings, it is likely that A. anserinus
recovery will depend on the successful re-colonization of burned areas.
Because of the generally low number of seedlings counted, where data
are available, we suspect that this re-colonization may take several
years and be dependent upon suitable environmental conditions.
We believe that wildfire frequency will increase within Astragalus
anserinus habitat. Wildfire return intervals in the sagebrush-steppe
ecosystem, which includes the Goose Creek drainage, have been
significantly reduced from between 60 and 110 years to often less than
5 years. The fact that the 2007 wildfire was the second wildfire
recorded within a 7-year period in the Goose Creek drainage, with no
previously recorded wildfires in this area, appears to present
supporting evidence for increased fire frequency. Wildfire kills
Astragalus anserinus, and seedling germination does not appear to be
stimulated by wildfire. Accordingly, increased fire frequency will
result in fewer A. anserinus individuals, and less seed availability
for recruitment. The ongoing and cumulative effects of wildfire on A.
anserinus include a substantial reduction in the amount of available
habitat, and range-wide population-level effects caused by the loss of
approximately 98 percent of the individual plants in the burned areas
(which were roughly 53 percent of the pre-2007 wildfire total known
individuals). Future wildfires in the area will likely result in
similar detrimental effects on the remaining population.
It is likely that Astragalus anserinus recovery will depend on the
successful re-colonization of burned areas, which will probably occur
slowly over time. However, because wildfire frequency has increased in
this area, recovery may be constrained by additional wildfires in the
relatively near future. Therefore, we find the magnitude of this threat
to be high.
Wildfire Management
Wildfire management can include prescribed burning, and activities
associated with fighting wildfires such as the construction of fire
lines and staging areas, retardant application, and post-wildfire
restoration efforts such as disking and seeding. In 2008, disking and
seeding associated with soil stabilization activities occurred over
portions of 11 Astragalus anserinus sites in Utah in response to the
2007 wildfire (Service 2008c, Tables 2-4, Map 4; Service, in litt.
2008, photos 1-3). It is likely that numerous individual plants were
lost to site re-seeding efforts and road construction activities. We
also observed in some cases that A. anserinus root systems had been
exposed, and believe that it is likely that individual plants were
turned over and buried during the disking operations. These actions
likely killed individual plants, thereby compounding the ongoing
detrimental effects of the wildfire itself on the A. anserinus
population.
Firefighting Activities
Firefighting activities such as prescribed burning, road and fire
line construction and retardant application can destroy habitat and
kill or injure individual Astragalus anserinus plants. Such activities
occurred during the response to the wildfire in 2007. Advance A.
anserinus surveys were not conducted because of the immediate need to
respond to the 2007 wildfire (M. Gates, Salt Lake City BLM, in litt.
2008a). During a brief field inspection of the area affected by
firefighting activities prior to our 2008 post-fire surveys, we
observed that at least one new road had been constructed along a ridge,
and that several fire lines had been excavated by hand adjacent to A.
anserinus habitat. We also observed that a wide fire line had been
constructed between 2 known EOs. During our 2008 post-wildfire surveys
over 18 A. anserinus occupied sites, we observed that fire retardant
had been applied at 1 site over an area approximately 10 ft (3 m) in
radius (U001-4-35). We also observed that a new access road had been
constructed through site U001-7-3, and evidence of tire tracks in
occupied areas at site U001-4-33.
One study of the effects of fire retardant chemical (Phos-Chek G75-
F) and fire suppressant foam (Silv-Ex) application, alone and in
combination with fire, on Great Basin shrub steppe vegetation found
that growth, resprouting, flowering, and incidence of galling insects
on Chrysothamnus viscidiflorus (yellow rabbitbrush) and Artemisia
tridenta (Big sagebrush) were not affected by any chemical treatment.
In general, the study found that species richness declined, especially
after Phos-Check application, but by the end of the growing season,
species richness did not differ between treated and control plots
(Larson et al. 1999, p. 115). We are unaware of the specific retardant
used in the 2007 fire response, or whether A. anserinus would be
similarly unaffected. However, based on the limited extent of the area
that was treated with retardant, we do not anticipate any significant
long-term impacts to the overall A. anserinus population. In addition,
since advance A. anserinus surveys were not conducted because of an
immediate need to respond to the wildfire, we do not know if the other
activities adversely affected the species. Some fire fighting
activities could present a future threat to A. anserinus, depending on
their specific location and scale; however, we are unable to assess the
magnitude of those potential threats at this time.
Post Wildfire Emergency Stabilization and Restoration
Post-wildfire restoration activities can also destroy habitat, kill
or harm individuals, and introduce nonnative species, which may
outcompete Astragalus anserinus for resources. The following is a
discussion of restoration activities that occurred after the 2008
fires.
2007 Wildfire Emergency Stabilization and Restoration in Nevada:
Following the 2007 wildfire season, the BLM Elko Nevada Field Office
(BLM-Nevada) developed a soil stabilization plan for implementation in
2008 that included reseeding several areas affected by the fire. A
native grass restoration seeding effort was planned near EO 005, but
was not conducted (Howard 2007, p 3). Post-fire aerial seeding of
Artemisia tridentata var. wyomingensis (Wyoming sagebrush), which is
native to Goose Creek, was undertaken within drainages at or near the
site instead of the native grass restoration seeding effort (K. Fuell,
Elko BLM, in litt. 2008, p. 1). This action may be beneficial to
Astragalus anserinus, however we are unaware of the specific treatment
locations, whether the efforts were successful, or whether they
affected A. anserinus in EO 005.
2007 Wildfire Emergency Stabilization and Restoration in Utah:
Restoration seeding activities in Utah were conducted in late May and
early June, 2008, as part of an Emergency Stabilization Plan (ESP) that
was developed by BLM to treat areas affected by the 2007 wildfire. A
fencing project and juniper removal chaining efforts (using a chain
connected between two tractors) were included as elements of this plan.
Under the ESP, disk seeding with a mix of native and nonnative species
(see ``Nonnative Invasive Species--seeded'' below) was conducted within
Astragalus anserinus habitat in an area west of Grouse Creek Road to
stabilize the soils, prevent erosion, and minimize competition by
Bromus tectorum (cheatgrass) in the burned area. Areas to be avoided
were identified in advance with flagging to
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prevent impacts to A. anserinus from planned juniper removal chaining
operations and seeding efforts (M. Gates, in litt. 2008b, p. 1).
However, not all A. anserinus sites were avoided.
The rangeland drills employed in the Utah