Endangered and Threatened Wildlife and Plants; Review of Native Species That Are Candidates for Listing as Endangered or Threatened; Annual Notice of Findings on Resubmitted Petitions; Annual Description of Progress on Listing Actions, 69222-69294 [2010-27686]
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DEPARTMENT OF THE INTERIOR
Fish and Wildlife Service
50 CFR Part 17
[Docket No. FWS–R9–ES–2010–0065; MO–
9221050083–B2]
Endangered and Threatened Wildlife
and Plants; Review of Native Species
That Are Candidates for Listing as
Endangered or Threatened; Annual
Notice of Findings on Resubmitted
Petitions; Annual Description of
Progress on Listing Actions
Fish and Wildlife Service,
Interior.
ACTION: Notice of review.
AGENCY:
In this Candidate Notice of
Review (CNOR), we, the U.S. Fish and
Wildlife Service (Service), present an
updated list of plant and animal species
native to the United States that we
regard as candidates for or have
proposed for addition to the Lists of
Endangered and Threatened Wildlife
and Plants under the Endangered
Species Act of 1973, as amended.
Identification of candidate species can
assist environmental planning efforts by
providing advance notice of potential
listings, allowing landowners and
resource managers to alleviate threats
and thereby possibly remove the need to
list species as endangered or threatened.
Even if we subsequently list a candidate
species, the early notice provided here
could result in more options for species
management and recovery by prompting
candidate conservation measures to
alleviate threats to the species.
The CNOR summarizes the status and
threats that we evaluated in order to
determine that species qualify as
candidates and to assign a listing
priority number (LPN) to each species or
to determine that species should be
removed from candidate status.
Additional material that we relied on is
available in the Species Assessment and
Listing Priority Assignment Forms
(species assessment forms, previously
called candidate forms) for each
candidate species.
Overall, this CNOR recognizes five
new candidates, changes the LPN for
four candidates, and removes one
species from candidate status.
Combined with other decisions for
individual species that were published
separately from this CNOR in the past
year, the current number of species that
are candidates for listing is 251.
This document also includes our
findings on resubmitted petitions and
describes our progress in revising the
Lists of Endangered and Threatened
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SUMMARY:
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Wildlife and Plants during the period
October 1, 2009, through September 30,
2010.
We request additional status
information that may be available for
the 251 candidate species identified in
this CNOR.
DATES: We will accept information on
any of the species in this Candidate
Notice of Review at any time.
ADDRESSES: This notice is available on
the Internet at https://
www.regulations.gov and https://
www.fws.gov/endangered/what-we-do/
cnor.html. Species assessment forms
with information and references on a
particular candidate species’ range,
status, habitat needs, and listing priority
assignment are available for review at
the appropriate Regional Office listed
below in SUPPLEMENTARY INFORMATION or
at the Branch of Candidate
Conservation, Arlington, VA (see
address below), or on our Web site
(https://ecos.fws.gov/tess_public/pub/
SpeciesReport.do?
listingType=C&mapstatus=1). Please
submit any new information, materials,
comments, or questions of a general
nature on this notice to the Arlington,
VA, address listed below. Please submit
any new information, materials,
comments, or questions pertaining to a
particular species to the address of the
Endangered Species Coordinator in the
appropriate Regional Office listed in
SUPPLEMENTARY INFORMATION.
FOR FURTHER INFORMATION CONTACT: The
Endangered Species Coordinator(s) in
the appropriate Regional Office(s), or
Chief, Branch of Candidate
Conservation, U.S. Fish and Wildlife
Service, 4401 N. Fairfax Drive, Room
420, Arlington, VA 22203 (telephone
703–358–2171; facsimile 703–358–
1735). Persons who use a
telecommunications device for the deaf
(TDD) may call the Federal Information
Relay Service (FIRS) at 800–877–8339.
SUPPLEMENTARY INFORMATION: We
request additional status information
that may be available for any of the
candidate species identified in this
CNOR. We will consider this
information to monitor changes in the
status or LPN of candidate species and
to manage candidates as we prepare
listing documents and future revisions
to the notice of review. We also request
information on additional species to
consider including as candidates as we
prepare future updates of this notice.
You may submit your information
concerning this notice in general or for
any of the species included in this
notice by one of the methods listed in
the ADDRESSES section.
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Species-specific information and
materials we receive will be available
for public inspection by appointment,
during normal business hours, at the
appropriate Regional Office listed below
under Request for Information in
SUPPLEMENTARY INFORMATION. General
information we receive will be available
at the Branch of Candidate
Conservation, Arlington, VA (see
address above).
Candidate Notice of Review
Background
The Endangered Species Act of 1973,
as amended (16 U.S.C. 1531 et seq.)
(Act), requires that we identify species
of wildlife and plants that are
endangered or threatened, based on the
best available scientific and commercial
information. As defined in section 3 of
the Act, an endangered species is any
species which is in danger of extinction
throughout all or a significant portion of
its range, and a threatened species is
any species which is likely to become
an endangered species within the
foreseeable future throughout all or a
significant portion of its range. Through
the Federal rulemaking process, we add
species that meet these definitions to
the List of Endangered and Threatened
Wildlife at 50 CFR 17.11 or the List of
Endangered and Threatened Plants at 50
CFR 17.12. As part of this program, we
maintain a list of species that we regard
as candidates for listing. A candidate
species is one for which we have on file
sufficient information on biological
vulnerability and threats to support a
proposal to list as endangered or
threatened, but for which preparation
and publication of a proposal is
precluded by higher priority listing
actions. We may identify a species as a
candidate for listing after we have
conducted an evaluation of its status on
our own initiative, or after we have
made a positive finding on a petition to
list a species, in particular we have
found that listing is warranted but
precluded by other higher priority
listing action (see the Petition Findings
section, below).
We maintain this list of candidates for
a variety of reasons: To notify the public
that these species are facing threats to
their survival; to provide advance
knowledge of potential listings that
could affect decisions of environmental
planners and developers; to provide
information that may stimulate and
guide conservation efforts that will
remove or reduce threats to these
species and possibly make listing
unnecessary; to request input from
interested parties to help us identify
those candidate species that may not
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require protection under the Act or
additional species that may require the
Act’s protections; and to request
necessary information for setting
priorities for preparing listing proposals.
We strongly encourage collaborative
conservation efforts for candidate
species, and offer technical and
financial assistance to facilitate such
efforts. For additional information
regarding such assistance, please
contact the appropriate Regional Office
listed under Request for Information or
visit our Web site, https://www.fws.gov/
endangered/what-we-do/cca.html.
Previous Notices of Review
We have been publishing candidate
notices of review (CNOR) since 1975.
The most recent CNOR (prior to this
CNOR) was published on November 9,
2009 (74 FR 57804). CNORs published
since 1994 are available on our Web
site, https://www.fws.gov/endangered/
what-we-do/cnor.html. For copies of
CNORs published prior to 1994, please
contact the Branch of Candidate
Conservation (see ADDRESSES section
above).
On September 21, 1983, we published
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, immediacy of
threats, and taxonomic status; the lower
the LPN, the higher the listing priority
(that is, a species with an LPN of 1
would have the highest listing priority).
Section 4(h)(3) of the Act (15 U.S.C.
1533(h)(3)) requires the Secretary to
establish guidelines for such a priorityranking guidance system. As explained
below, in using this system we first
categorize based on the magnitude of
the threat(s), then by the immediacy of
the threat(s), and finally by taxonomic
status.
Under this priority-ranking system,
magnitude of threat can be either ‘‘high’’
or ‘‘moderate to low.’’ This criterion
helps ensure that the species facing the
greatest threats to their continued
existence receive the highest listing
priority. It is important to recognize that
all candidate species face threats to their
continued existence, so the magnitude
of threats is in relative terms. For all
candidate species, the threats are of
sufficiently high magnitude to put them
in danger of extinction, or make them
likely to become in danger of extinction
in the foreseeable future. But for species
with higher magnitude threats, the
threats have a greater likelihood of
bringing about extinction or are
expected to bring about extinction on a
shorter time scale (once the threats are
imminent) than for species with lower
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magnitude threats. Since we do not
routinely quantify how likely or how
soon extinction would be expected to
occur absent listing, we must evaluate
factors that contribute to the likelihood
and time scale for extinction. We
therefore consider information such as:
The number of populations and/or
extent of range of the species affected by
the threat(s); the biological significance
of the affected population(s), taking into
consideration the life-history
characteristics of the species and its
current abundance and distribution;
whether the threats affect the species in
only a portion of its range, and if so the
likelihood of persistence of the species
in the unaffected portions; the severity
of the effects and the rapidity with
which they have caused or are likely to
cause mortality to individuals and
accompanying declines in population
levels; whether the effects are likely to
be permanent; and the extent to which
any ongoing conservation efforts reduce
the severity of the threat.
As used in our priority-ranking
system, immediacy of threat is
categorized as either ‘‘imminent’’ or
‘‘nonimminent’’ and is not a measure of
how quickly the species is likely to
become extinct if the threats are not
addressed; rather, immediacy is based
on when the threats will begin. If a
threat is currently occurring or likely to
occur in the very near future, we
classify the threat as imminent.
Determining the immediacy of threats
helps ensure that species facing actual,
identifiable threats are given priority for
listing proposals over those for which
threats are only potential or species that
are intrinsically vulnerable to certain
types of threats but are not known to be
presently facing such threats.
Our priority ranking system has three
categories for taxonomic status: Species
that are the sole members of a genus;
full species (in genera that have more
than one species); and subspecies and
distinct population segments of
vertebrate species (DPS). We also apply
this last category to species that are
threatened or endangered in only
significant portions of their ranges
rather than their entire ranges.
The result of the ranking system is
that we assign each candidate a listing
priority number of 1 to 12. For example,
if the threat(s) is of high magnitude,
with immediacy classified as imminent,
the listable entity is assigned an LPN of
1, 2, or 3 based on its taxonomic status
(i.e., a species that is the only member
of its genus would be assigned to the
LPN 1 category, a full species to LPN 2,
and a subspecies, DPS, or a species that
is threatened or endangered in only a
significant portion of its range would be
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assigned to LPN 3). In summary, the
LPN ranking system provides a basis for
making decisions about the relative
priority for preparing a proposed rule to
list a given species. No matter which
LPN we assign to a species, each species
included in this notice as a candidate is
one for which we have sufficient
information to prepare a proposed rule
to list it because it is in danger of
extinction or likely to become
endangered within the foreseeable
future throughout all or a significant
portion of its range.
For more information on the process
and standards used in assigning LPNs,
a copy of the 1983 guidance is available
on our Web site at: https://www.fws.gov/
endangered/esa-library/pdf/48fr4309843105.pdf. For more information on the
LPN assigned to a particular species, the
species assessment for each candidate
contains the LPN chart and a rationale
for the determination of the magnitude
and immediacy of threat(s) and
assignment of the LPN; that information
is summarized in this CNOR.
This revised notice supersedes all
previous animal, plant, and combined
candidate notices of review.
Summary of This CNOR
Since publication of the previous
CNOR on November 9, 2009 (74 FR
57804), we reviewed the available
information on candidate species to
ensure that a proposed listing is
justified for each species, and
reevaluated the relative LPN assigned to
each species. We also evaluated the
need to emergency-list any of these
species, particularly species with high
priorities (i.e., species with LPNs of 1,
2, or 3). This review and reevaluation
ensures that we focus conservation
efforts on those species at greatest risk
first.
In addition to reviewing candidate
species since publication of the last
CNOR, we have worked on numerous
findings in response to petitions to list
species, and on proposed and final
determinations for rules to list species
under the Act. Some of these findings
and determinations have been
completed and published in the Federal
Register, while work on others is still
under way (see Preclusion and
Expeditious Progress, below, for details).
Based on our review of the best
available scientific and commercial
information, with this CNOR we
identify five new candidate species (see
New Candidates, below), change the
LPN for four candidates (see Listing
Priority Changes in Candidates, below)
and determine that a listing proposal is
not warranted for one species and thus
remove it from candidate status (see
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Candidate Removals, below). Combined
with the other decisions published
separately from this CNOR for
individual species that previously were
candidates, a total of 251 species
(including 110 plant and 141 animal
species) are now candidates awaiting
preparation of rules proposing their
listing. These 251 species, along with
the 18 species currently proposed for
listing (includes 1 species proposed for
listing due to similarity in appearance),
are included in Table 1.
Table 2 lists the changes from the
previous CNOR, and includes 55 species
identified in the previous CNOR as
either proposed for listing or classified
as candidates that are no longer in those
categories. This includes 54 species for
which we published a final rule to list,
plus the 1 species that we have
determined does not meet the definition
of endangered or threatened and
therefore does not warrant listing. We
have removed this species from
candidate status in this CNOR.
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New Candidates
Below we present a brief summary of
one new fish, one new snail, one new
crustacean, and two new plant
candidates, which we are recognizing in
this CNOR. Complete information,
including references, can be found in
the species assessment forms. You may
obtain a copy of these forms from the
Regional Office having the lead for the
species, or from our Web site (https://
ecos.fws.gov/tess_public/pub/
SpeciesReport.do?listingType=C
&mapstatus=1). For these species, we
find that we have on file sufficient
information on biological vulnerability
and threats to support a proposal to list
as endangered or threatened, but that
preparation and publication of a
proposal is precluded by higher priority
listing actions (i.e., it met our definition
of a candidate species). We also note
below that nine other species—
Sprague’s pipit, greater sage-grouse,
Bi-State DPS of greater sage-grouse,
Gunnison sage-grouse, least chub, upper
Missouri River DPS of Arctic grayling,
Tucson shovel-nosed snake, Jemez
Mountains salamander, and Agave
eggersiana—were identified as
candidates earlier this year as a result of
separate petition findings published in
the Federal Register.
Birds
Sprague’s pipit (Anthus spragueii)—
We previously announced candidate
status for this species, and described the
reasons and data on which the finding
was based, in a separate warranted-butprecluded 12-month petition finding
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published on September 14, 2010 (75 FR
56028).
Greater sage-grouse (Centrocercus
urophasianus)—We previously
announced candidate status for this
species, and described the reasons and
data on which the finding was based, in
a separate warranted-but-precluded
12-month petition finding published on
March 23, 2010 (75 FR 13910).
Greater sage-grouse, Bi-State DPS
(Centrocercus urophasianus)—We
previously announced candidate status
for this species, and described the
reasons and data on which the finding
was based, in a separate warranted-butprecluded 12-month petition finding
published on March 23, 2010 (75 FR
13910).
Gunnison sage-grouse (Centrocercus
minimus)—We previously announced
candidate status for this species, and
described the reasons and data on
which the finding was based, in a
separate warranted-but-precluded
12-month petition finding published on
September 28, 2010 (75 FR 59803).
Reptiles
Tucson Shovel-Nosed Snake
(Chionactis occipitalis klauberi)—We
previously announced candidate status
for this species, and described the
reasons and data on which the finding
was based, in a separate warranted-butprecluded 12-month petition finding
published on March 31, 2010 (75 FR
16050).
Amphibians
Jemez Mountains salamander
(Plethodon neomexicanus)—We
previously announced candidate status
for this species, and described the
reasons and data on which the finding
was based, in a separate warranted-butprecluded 12-month petition finding
published on September 9, 2010 (75 FR
54822).
Fish
Least chub (Iotichthys
phlegethontis)—We previously
announced candidate status for this
species, and described the reasons and
data on which the finding was based, in
a separate warranted-but-precluded
12-month petition finding published on
June 22, 2010 (75 FR 35398).
Kentucky arrow darter (Etheostoma
sagitta spilotum)—The following
summary is based on information in our
files. The Kentucky arrow darter is a
rather large (total length of 4.6 inches
(116 millimeters)), brightly colored
darter that is restricted to the upper
Kentucky River basin in eastern
Kentucky. The species’ preferred habitat
consists of pools or transitional areas
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between riffles and pools (runs and
glides) in moderate to high gradient
streams with bedrock, boulder, and
cobble substrates. In most recent
surveys, the Kentucky arrow darter has
been observed in streams ranging in size
from first to third order, with most
individuals occurring in second order
streams in watersheds encompassing 7.7
square miles (20 square kilometers) or
less. Kentucky arrow darters feed on a
variety of aquatic invertebrates, but
adults feed predominantly on larval
mayflies (order Ephemeroptera),
specifically the families Heptageniidae
and Baetidae. Rangewide surveys from
2007 to 2009 revealed that the Kentucky
arrow darter has disappeared from
portions of its range. During these
surveys, the species was observed at
only 33 of 68 historical streams and 45
of 100 historical sites.
The subspecies’ habitat and range
have been severely degraded and
limited by water pollution from surface
coal mining and gas-exploration
activities; removal of riparian
vegetation; stream channelization;
increased siltation associated with poor
mining, logging, and agricultural
practices; and deforestation of
watersheds. The threats are high in
magnitude because they are widespread
across the subspecies’ range. In
addition, the magnitude (severity or
intensity) of these threats, especially
impacts from mining and gasexploration activities, is high because
these activities have the potential to
alter stream water quality permanently
throughout the range by contributing
sediment, dissolved metals, and other
solids to streams supporting Kentucky
arrow darters, resulting in direct
mortality or reduced reproductive
capacity. The threats are imminent
because the effects are manifested
immediately and will continue for the
foreseeable future. Consequently, we
assigned an LPN of 3 to this subspecies.
Arctic grayling, Missouri River DPS
(Thymallus arcticus)—We previously
announced candidate status for this
species, and described the reasons and
data on which the finding was based, in
a separate warranted-but-precluded
12-month petition finding published on
September 8, 2010 (75 FR 54707).
Snails
Rosemont talussnail (Sonorella
rosemontensis)—the following summary
is based on information in our files. The
petition we received on June 24, 2010,
provided no new information beyond
what we had already included in our
assessment of this species. The
Rosemont talussnail, a land snail in the
family Helminthoglyptidae, is known
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from three talus slopes in the Santa Rita
Mountains, Pima County, Arizona. The
primary threat to Rosemont talussnail is
hard rock mining. The entire range of
the species is located on patented
mining claims and can reasonably be
expected to be subjected to mining
activities in the foreseeable future. Hard
rock mining typically involves the
blasting of hillsides and the crushing of
ore-laden rock. Such activities would
kill talussnails and render their habitats
unsuitable for occupation. Since mining
may occur across the entire range of the
species within the foreseeable future,
potentially resulting in rangewide
habitat destruction and population
losses, the threats are of a high
magnitude. However, mining on
patented mining claims, although a
reasonably anticipated action, is neither
currently ongoing nor imminent.
Although the Rosemont Copper Mine is
scheduled to commence as soon as
2011, there exists uncertainty regarding
its scope, and therefore its potential
effect on habitat of the Rosemont
talussnail. Accordingly, we find that
overall threats to the Rosemont
talussnail are nonimminent and we
assign an LPN of 5 to this species.
Crustaceans
Kenk’s amphipod (Stygobromus
kenki)—Amphipods of the genus
Stygobromus, occur in groundwater and
groundwater-related habitats. In the case
of Kenk’s amphipod, these include
seeps, small springs, and possibly wells.
Kenk’s amphipod is a small, eyeless,
unpigmented crustacean adapted for
survival in subterranean habitats. It can
be found in dead leaves or fine sediment
submerged in the waters of its spring/
seep outflows. The species is currently
known only from five spring or seep
sites in Washington, DC, and
Montgomery County, Maryland. Four of
these sites are within the Rock Creek
drainage, and the fifth is within the
Northwest Branch drainage.
Within the limited area encompassing
the current range of this species, the
vast majority of potential expanses of
habitat large enough to support this
species have been significantly
impacted or completely destroyed by
urban and suburban development.
Kenk’s amphipod is now vulnerable
because of its limited geographic
distribution and infringement of urban
development on its habitat. Degradation
of water quality and modifications of
hydrology are among the principal
threats to this species’ spring or seep
habitats. Specific threats include toxic
spills, non-point source pollution,
sanitary sewer leaks, excessive
stormwater flows, and additional land
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disturbance. In addition, climate change
has the potential to adversely affect the
species, particularly if it results in a
significant change in the amount of
precipitation in the Washington, DC,
area.
Although all five known sites of
occurrence face threats to the hydrology
and water quality of their springs, these
threats are chronic in nature and appear
to be increasing only gradually and are
not currently resulting in major
mortality events or impairment of
reproduction. Thus, the threats are
moderate in magnitude. Several threats
are imminent because they are ongoing
and expected to continue. Therefore, we
assigned this species LPN of 8.
Flowering Plants
Agave eggersiana (no common
name)—We previously announced
candidate status for this species, and
described the reasons and data on
which the finding was based, in a
separate warranted-but-precluded
12-month petition finding published on
September 22, 2010 (75 FR 57720).
Astragalus cusickii var. packardiae
(Packard’s milkvetch)—The following
summary is based on information
contained in our files. This plant is a
narrow endemic located in northeastern
Payette County, Idaho. Its entire known
range is only approximately 10 square
miles (26 square kilometers). The lightcolored, sparsely vegetated sedimentary
outcrops to which this species is
restricted are found scattered
throughout the landscape, but are
limited in extent. The size of occupied
outcrops ranges from less than 0.04
hectares (0.1 acre) to approximately 1.2
hectares (3 acres). The entire population
of A. cusickii var. packardiae is
currently estimated at 5,000 plants
located within 26 occurrences (17 on
Bureau of Land Management, 4 on State,
and 5 on private land).
The primary threats to Astragalus
cusickii var. packardiae include
wildfire, nonnative invasive plant
species, and more recently, off-road
vehicle (ORV) use. Vegetation within
the range of A. cusickii var. packardiae
was originally sagebrush-steppe habitat;
however, due to habitat impacts from a
century of wildfires, livestock use, and
invasive nonnative plant species, much
of the area has been converted to annual
grassland dominated by two nonnative
grass species, Bromus tectorum
(cheatgrass) and Taeniatherum caputmedusae (medusahead). Invasive
nonnative plants affect A. cusickii var.
packardiae directly through
competition and indirectly by providing
continuous fine fuels that contribute to
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the increased frequency and extent of
wildfires.
ORV use, which is currently
considered the most immediate threat to
Astragalus cusickii var. packardiae and
its habitat, was not identified as a threat
during the original 1999 surveys for this
species, but monitoring conducted in
2008 and 2009 indicate it has since
become a widespread activity, occurring
throughout the limited range of A.
cusickii var. packardiae. ORVs are
traveling directly through outcrops
occupied by A. cusickii var. packardiae,
as well as along the rims, spur ridges,
and slope bases that form the margins of
the occupied outcrops, with tracks
ranging from single passage treads to
major hill climbing runways. Based on
monitoring data, this use appears to be
increasing in scope and has resulted in
the crushing of A. cusickii var.
packardiae plants, as well as
accelerated erosion of the fine, loose
substrate occupied by this species.
Based on this information, the
magnitude of the primary threats to
Astragalus cusickii var. packardiae and
its habitat is high because ORV use,
wildfires, and nonnative invasive
species affect the species throughout its
range, appear to be increasing in extent,
and result in severe and direct impacts
to individuals and population levels.,
Because these threats are ongoing
throughout A. cusickii var. packardiae’s
limited range, these threats are
imminent. Thus, we assign an LPN of 3
to this plant variety.
Mimulus fremontii var.
vandenbergensis (Vandenberg
monkeyflower)—Mimulus fremontii var.
vandenbergensis is a small, short-lived
annual herb in the Phrymaceae family
(no common family name). It ranges
from 0.5 to 10 inches (1 to 20
centimeters) tall and produces flowers
that are bright yellow with reddish
brown markings near the mouth. The
seeds are small and numerous, and seed
is likely dispersed by the wind as the
seed pods open. As with other annual
species that are sensitive to annual
levels of rainfall, germination of
resident seed banks may be low or
nonexistent in unfavorable years, with
little or no aboveground expression of
the species visible.
Mimulus fremontii var.
vandenbergensis occurs only in western
Santa Barbara County, California, at
lower elevations and closer to the coast,
in sandy openings of coastal scrub,
chaparral, and woodlands on an old
dune sheet known as Burton Mesa.
Seven populations occur across the
mesa over a distance of approximately
6 miles, generally in alignment with the
prevailing winds. Two populations
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occur on Vandenberg Air Force Base,
two occur on State Park lands at La
Purisima State Historic Park, two occur
primarily on Department of Fish and
Game lands on Burton Mesa Ecological
Reserve, and one occurs primarily on
private lands.
The threats currently facing Mimulus
fremontii var. vandenbergensis include
alteration and destruction of habitat
from development and associated
secondary impacts, including increased
fragmentation, alteration of hydrology,
competition with nonnative species,
and alteration of fire regimes. The taxon
is also threatened with stochastic
extinction due to small population size:
Of the 7 populations, 3 have supported
fewer than 100 individuals based on at
least 2 years of observations. We
consider competition with nonnative
plant species to be the largest and most
immediate threat: Veldt grass, pampas
grass, bromes, Sahara mustard, star
thistle, Italian thistle, and bull thistle
are present at various sites where
Mimulus fremontii var. vandenbergensis
occurs. Habitat for one population on
private land was graded in 2007 in
preparation for construction of a
housing development. Construction has
been stalled, and in the meantime, veldt
grass has become established in the
graded lot and has increased the rate at
which this species is spreading in
adjacent habitat for Mimulus fremontii
var. vandenbergensis, including the
Burton Mesa Ecological Reserve. Veldt
grass is also present and rapidly
spreading at population sites on
Vandenberg Air Force Base and La
Purisima State Historic Park.
The threats are of a high magnitude
because all three of the largest
populations are at risk of being lost from
the invasion of nonnative species. The
third largest population is also
threatened by secondary impacts from a
planned development and firefighting
activities. Losses of some or all of the
three largest populations will increase
the risk of extinction of the taxon as a
whole because the remaining
populations are smaller and more
vulnerable to stochastic extirpation,
which compounds the other threats
these small populations face. The
threats are ongoing and, therefore,
imminent. Consequently, we have
assigned a LPN of 3 to this plant variety.
Listing Priority Changes in Candidates
We reviewed the LPN for all
candidate species and are changing the
numbers for the following species
discussed below. Some of the changes
reflect actual changes in either the
magnitude or immediacy of the threats.
For some species, the LPN change
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reflects efforts to ensure national
consistency as well as closer adherence
to the 1983 guidelines in assigning these
numbers, rather than an actual change
in the nature of the threats.
Snails
Page springsnail (Pyrgulopsis
morrisoni)—The following summary is
based on information contained in our
files. The Page springsnail is known to
exist only within a complex of springs
located within an approximately 0.93mi (1.5-km) stretch along the west side
of Oak Creek around the community of
Page Springs, and within springs
located along Spring Creek, tributary to
Oak Creek, Yavapai County, Arizona.
The primary threat to the Page
springsnail is modification of habitat by
domestic, agricultural, ranching, fish
hatchery, and recreational activities.
Many of the springs where the species
occurs have been subjected to some
level of such modification. Based on
recent survey data, it appears that the
Page springsnail is abundant within
natural habitats and persists in modified
habitats, albeit at reduced densities.
Arizona Game and Fish Department
(AGFD) management plans for the
Bubbling Ponds and Page Springs fish
hatcheries include commitments to
replace lost habitat and to monitor
remaining populations of invertebrates
such as the Page springsnail. The AGFD
and the Service recently entered into a
Candidate Conservation Agreement with
Assurances that calls for evaluating the
restoration and creation of natural
springhead integrity, including springs
on AGFD properties. In fact, several
conservation measures have already
been implemented. Also, the National
Park Service recently acquired Shea
Springs, a site that the Page springsnail
occupied historically, and has expressed
an interest in restoring natural
springhead integrity to that site.
Accordingly, implementation of the
CCAA reduces the magnitude of threats
to a moderate level and greatly reduces
the chances of extirpation or extinction.
The immediacy of the threat of
groundwater withdrawal is uncertain,
due to conflicting information regarding
imminence. However, overall, the
threats are imminent, because
modification of the species’ habitat by
threats other than groundwater
withdrawal is currently occurring.
Therefore, we are changing the LPN for
the Page springsnail from a 2 to an 8.
Flowering Plants
Hibiscus dasycalyx (Neches River
rose-mallow)—The following summary
is based on information contained in
our files. This species, found in eastern
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Texas, appears to be restricted to those
portions of wetlands that are exposed to
open sun and normally hold standing
water early in the growing season, with
water levels dropping during late
summer and fall. This habitat has been
affected by drainage or filling of
floodplain depressions and oxbows,
stream channelization, road
construction, timber harvesting,
agricultural activities (primarily
mowing and grazing), and herbicide use.
Threats that continue to affect the
species include wetland alteration,
herbicide use, grazing, mowing during
the species’ growing and flowering
period, and genetic swamping by other
Hibiscus species.
A 1995 status survey of 10 counties
resulted in confirmation of the species
at only three sites, but in three separate
counties and three different watersheds,
suggesting a relatively wide historical
range. These three populations were all
within highway rights-of-way and
vulnerable to herbicides and adjacent
agricultural activities. As of 2005, only
20 plants remained at one of these sites.
Additional surveys for Hibiscus
dasycalyx discovered new populations.
About 300 plants were found on land
owned by Temple-Inland Corporation in
east Trinity County. Smaller plant
numbers have been seen at this site and
in 2005 no plants were observed. This
site may be too dry to support this
species, possibly due to changes in the
wetland’s hydrology. Another site
discovered on land previously owned
by Champion International Corporation
(near White Rock Creek in west Trinity
County) once supported 300–400 plants.
This site was modified in 2007. In west
Houston County, a population of 300 to
400 plants discovered on private land
has been purchased by the Natural Area
Preservation Association in order to
protect this land in perpetuity. In east
Houston County, a population
discovered in Compartment 55 in Davy
Crockett National Forest numbered over
1,000 in 2006. In 2000, nearly 800
plants were introduced into
Compartments 16 and 20 of Davy
Crockett National Forest as part of a
reintroduction effort. One population
retained high numbers (350 in 2006),
but was subjected to high water
conditions in 2007 and may have been
adversely affected. The second site was
affected by a change in hydrology and
had declined to 50 plants in 2006. In
2004, 200 plants were placed in a
wetland in Compartment 11 of Davy
Crockett National Forest, but only 10
plants were seen in 2006. High water
from heavy spring and summer rains
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prevented further assessment of these
rose-mallow sites.
The threats to the species continue to
be of a high magnitude because all of
the populations are severely affected by
some combination of the threats, and
the effectiveness of the re-introduction
and preservation efforts has not been
established. After evaluating the current
conditions of the species’ habitat, we
now find that threats are imminent
overall. Threats are currently occurring
and ongoing for nearly all of the
populations (herbicides and adjacent
agricultural activities for the 3
populations identified in 1995, and
hydrology alteration and other
modifications for the 2 populations in
east Trinity County and the 3
populations reintroduced in Davy
Crockett National Forest). Thus, in light
of this information and to ensure
consistency in the application of our
listing priority process we have changed
the LPN from a 5 to a 2 for the Neches
River rose-mallow to reflect imminent
threats of high magnitude.
Linum arenicola (Sand flax)—The
following summary is based on
information contained in our files. Sand
flax is found in pine rockland and marl
prairie habitats, which require periodic
wildfires in order to maintain an open,
shrub-free subcanopy and reduce leaflitter levels. Based upon available data,
there are 11 extant occurrences of sand
flax; 11 others have been extirpated or
destroyed. For the most part, only small
and isolated occurrences remain in low
lying areas in a restricted range of
southern Florida and the Florida Keys.
In general, viability is uncertain for 9 of
11 occurrences.
Sand flax is threatened by habitat loss
and degradation due to development;
climatic changes and sea-level rise,
which ultimately are likely to
substantially reduce the extent of
available habitat; fire suppression and
difficulty in applying prescribed fire;
road maintenance activities; exotic
species; illegal dumping; natural
disturbances, such as hurricanes,
tropical storms, and storm surges; and
the small and fragmented nature of the
current population. Reduced pollinator
activity and suppression of pollinator
populations from pesticides used in
mosquito control and decreased seed
production due to increased seed
predation in a fragmented wildland
urban interface may also affect sand
flax; however, not enough information
is known on this species’ reproductive
biology or life history to assess these
potential threats. Some of the threats to
the species—including fire suppression,
difficulty in applying prescribed fire,
road maintenance activities, exotic
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species, and illegal dumping—threaten
nearly all remaining populations.
However, some efforts are under way to
use prescribed fire to control exotics on
conservation lands where this species
occurs.
There are some circumstances that
may mitigate the impacts of the threats
upon the species. For example, a survey
conducted in 2009 showed
approximately 74,000 plants on a nonconservation, public site in Miami-Dade
County; this is far more plants than was
previously known. Although a portion
of the plants will be affected by
development, approximately 60,000 are
anticipated to be protected and managed
through a Conservation Easement.
Consequently, the majority of the largest
occurrence in Miami-Dade County is
expected to be conserved and managed.
In addition, much of the pine rockland
on Big Pine Key, the location of the
largest occurrence in the Keys, is
protected from development.
Nevertheless, due to the small and
fragmented nature of the current
population, stochastic events, disease,
or genetic bottlenecks may strongly
affect this species in the Keys. One
example is Hurricane Wilma, which
inundated most of the species’ habitat
on Big Pine Key in 2005, and plants
were not found 8–9 weeks post-storm;
the density of sand flax declined to zero
in all management units at The Nature
Conservancy’s preserve in 2006. In a
2007 post-hurricane assessment, sand
flax was found in northern plots, but not
in any of the southern plots on Big Pine
Key. More current data are not available.
Overall, the magnitude of threats is
high, because the threats affect all 11
known occurrences of the species, and
can result in a precipitous decline to the
population levels, particularly when
combined with the potential impacts
from hurricanes or other natural
disasters. Because development is not
immediate for the majority of the largest
population in Miami-Dade County and
another population in the Keys is also
largely protected from development
since much of it is within public and
private conservation lands, the threat of
habitat loss is now nonimminent. In
addition, sea level rise is a long-term
threat since we do not have evidence
that it is currently affecting any
population of sand flax. Therefore,
based upon new information (new
survey date showing a much larger
population of plants), and reduced
immediacy of threats, we changed the
LPN of this species from a 2 to a 5.
Penstemon scariosus var. albifluvis
(White River beardtongue)—The
following summary is based on
information contained in our files and
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the petition we received on October 27,
1983. This species is restricted to
calcareous soils derived from oil shale
barrens of the Green River Formation in
the Uinta Basin of northeastern Utah
and adjacent Colorado. There are 14
occurrences known in Utah and 1 in
Colorado. Most of the occupied habitat
of the White River beardtongue is
within developed and expanding oil
and gas fields. The location of the
species’ habitat exposes it to destruction
from road, pipeline, and well site
construction in connection with oil and
gas development. Recreational off-road
vehicle use, heavy grazing by livestock,
and wildlife and livestock trampling are
additional threats. A future threat (and
potentially the greatest threat) to the
species is oil shale development.
In the 2009 CNOR, we found the
threats were nonimminent and high
magnitude. However, traditional oil and
gas energy development in the area has
expanded into habitat for this species,
and therefore the threat is now
imminent. In addition, BLM has
adopted a Special Status Species policy
and has included in its current Resource
Management Plan commitments to
protect this species. These protections
lessen the extent of traditional oil and
gas development impacts to this species,
so that the threat is now of moderate
magnitude. The threat from off-road
vehicles is also moderate because BLM
limited all vehicles to designated routes,
thus avoiding beardtongue habitat.
Based on current information, we are
changing the LPN from a 6 to a 9 for this
plant variety.
Candidate Removals
As summarized below, we have
evaluated the threats to the following
species and considered factors that,
individually and in combination,
currently or potentially could pose a
risk to this species and its habitat. After
a review of the best available scientific
and commercial data, we conclude that
listing this species under the
Endangered Species Act is not
warranted because the species is not
likely to become an endangered species
within the foreseeable future throughout
all or a significant portion of its’ range.
Therefore, we find that proposing a rule
to list it is not warranted, and we no
longer consider it to be a candidate
species for listing. We will continue to
monitor the status of this species and to
accept additional information and
comments concerning this finding. We
will reconsider our determination in the
event that new information indicates
that the threats to the species is of a
considerably greater magnitude or
imminence than identified through
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assessments of information contained in
our files, as summarized here.
Mammals
Palm Springs round-tailed ground
squirrel (Xerospermophilus tereticaudus
chlorus)—The following summary is
based on information contained in our
files. No new information was provided
in the petition we received on May 11,
2004. The Palm Springs round-tailed
ground squirrel was believed to be
limited in range to the Coachella Valley
region of Riverside County, California.
The primary habitat in the Coachella
Valley for round-tailed ground squirrel
is the dunes and mesquite hummocks
associated with Prosopis glandulosa var.
torreyana (honey mesquite) and to a
lesser extent those dunes and
hummocks associated with Larrea
tridentata (creosote), or other
vegetation. The primary threat to
X. t. chlorus in the Coachella Valley was
from habitat loss due to urban
development and drops in the
groundwater table, which eliminated
much of the honey mesquite in the
Coachella Valley and fragmented habitat
occupied by this subspecies. The
Coachella Valley Association of
Governments (CVAG) developed a
Multiple Species Habitat Conservation
Plan (MSHCP) that was reviewed and
approved by the Service in 2008.
Habitat conservation and monitoring
actions that have been implemented
since 2008 specifically for X. t. chlorus
have significantly eliminated the threat
of urban development to the taxon. To
date, conservation for X. t. chlorus
includes protection of 244 acres of
mesquite hummocks as a result of the
MSHCP, in addition to 104 acres of
mesquite hummocks on conservation
lands in existence prior to permitting
the MSHCP. Protection of additional
habitat (desert shrub communities and
other sandy areas with appropriate
vegetation known to harbor the
subspecies at lower densities) is also
anticipated in other portions of the plan
area. Although we do not rely upon
future implementation of the additional
habitat protections anticipated in the
MSHCP, we do expect conservation
actions specific to X. t. chlorus to
continue as a result of the commitment
by CVAG and the MSHCP.
More significant than the ongoing
conservation measures is the fact that
recent results of both morphological and
genetic studies indicate its range is
substantially larger than previously
believed. Analysis of experimental
samples show X. t. chlorus is found in
Hinkley Valley and Death Valley,
expanding the range at minimum 150
miles northward. Because X. t. chlorus
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is more widespread in its range than
was previously understood, and based
on our review of the best available
information, we no longer conclude that
threats across this newly expanded
range put the taxon in danger of
extinction. Moreover, this subspecies is
not endangered or threatened in a
significant portion of the range because
the conservation actions and current
protections provided in Death Valley
make it so it is not endangered or
threatened in any portion of the range.
In summary, the existing conservation
provided by MSHCP in the Coachella
Valley, along with the data showing the
subspecies has an expanded range over
which the threats are nonsignificant to
the taxon as a whole, we find listing of
the Palm Springs round-tailed ground
squirrel (X. t. chlorus) throughout all or
a significant portion of its range is no
longer warranted. The subspecies no
longer meets our definition of a
candidate, and we have removed it from
candidate status.
Petition Findings
The Act provides two mechanisms for
considering species for listing. One
method allows the Secretary, on his
own initiative, to identify species for
listing under the standards of section
4(a)(1). We implement this through the
candidate program, discussed above.
The second method for listing a species
provides a mechanism for the public to
petition us to add a species to the Lists.
The CNOR serves several purposes as
part of the petition process: (1) In some
instances (in particular, for petitions to
list species that the Service has already
identified as candidates on its own
initiative), it serves as the petition
finding; (2) it serves as a ‘‘resubmitted’’
petition finding that the Act requires the
Service to make each year; and (3) it
documents the Service’s compliance
with the statutory requirement to
monitor the status of species for which
listing is warranted-but-precluded to
ascertain if they need emergency listing.
First, the CNOR serves as a petition
finding in some instances. Under
section 4(b)(3)(A), when we receive a
listing petition, we must determine
within 90 days, to the maximum extent
practicable, whether the petition
presents substantial information
indicating that listing may be warranted
(a ‘‘90-day finding’’). If we make a
positive 90-day finding, we must
promptly commence a status review of
the species under section 4(b)(3)(A); we
must then make and publish one of
three possible findings within
12 months of the receipt of the petition
(a ‘‘12-month finding’’):
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1. The petitioned action is not
warranted;
2. The petitioned action is warranted
(in which case we are required to
promptly publish a proposed regulation
to implement the petitioned action;
once we publish a proposed rule for a
species, section 4(b)(5) and 4(b)(6)
govern further procedures regardless of
whether we issued the proposal in
response to a petition); or
3. The petitioned action is warranted
but (a) the immediate proposal of a
regulation and final promulgation of a
regulation implementing the petitioned
action is precluded by pending
proposals to determine whether any
species is endangered or threatened, and
(b) expeditious progress is being made
to add qualified species to the lists of
endangered or threatened species.
(We refer to this third option as a
‘‘warranted-but-precluded finding.’’)
We define ‘‘candidate species’’ to
mean those species for which the
Service has on file sufficient
information on biological vulnerability
and threat(s) to support issuance of a
proposed rule to list, but for which
issuance of the proposed rule is
precluded (61 FR 64481; December 6,
1996). This standard for making a
species a candidate through our own
initiative is identical to the standard for
making a warranted-but-precluded
12-month petition finding on a petition
to list, and we add all petitioned species
for which we have made a warrantedbut-precluded 12-month finding to the
candidate list.
Therefore all candidate species
identified through our own initiative
already have received the equivalent of
substantial 90-day and warranted-butprecluded 12-month findings.
Nevertheless, we review the status of
the newly petitioned candidate species
and through this CNOR publish specific
section 4(b)(3) findings (i.e., substantial
90-day and warranted-but-precluded
12-month findings) in response to the
petitions to list these candidate species.
We publish these findings as part of the
first CNOR following receipt of the
petition. Since publication of the CNOR
in 2009, we received petitions to list
three candidate species, the Florida
bonneted bat, headwater chub, and
Rosemont talussnail (we received this
petition after we initiated our
assessment of this species for candidate
status). We are making substantial
90-day findings and warranted-butprecluded 12-month findings for these
species as part of this notice. We have
identified the candidate species for
which we received petitions by the code
‘‘C*’’ in the category column on the left
side of Table 1.
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Second, the CNOR serves as a
‘‘resubmitted’’ petition finding. Section
4(b)(3)(C)(i) of the Act requires that
when we make a warranted-butprecluded finding on a petition, we are
to treat such a petition as one that is
resubmitted on the date of such a
finding. Thus, we must make a 12month petition finding in compliance
with section 4(b)(3)(B) of the Act at least
once a year, until we publish a proposal
to list the species or make a final notwarranted finding. We make these
annual findings for petitioned candidate
species through the CNOR.
Third, through undertaking the
analysis requires to complete the CNOR,
the Service determines if any candidate
species needs emergency listing. Section
4(b)(3)(C)(iii) of the Act requires us to
‘‘implement a system to monitor
effectively the status of all species’’ for
which we have made a warranted-butprecluded 12-month finding, and to
‘‘make prompt use of the [emergency
listing] authority [under section 4(b)(7)]
to prevent a significant risk to the well
being of any such species.’’ The CNOR
plays a crucial role in the monitoring
system that we have implemented for all
candidate species by providing notice
that we are actively seeking information
regarding the status of those species. We
review all new information on
candidate species as it becomes
available, prepare an annual species
assessment form that reflects monitoring
results and other new information, and
identify any species for which
emergency listing may be appropriate. If
we determine that emergency listing is
appropriate for any candidate we will
make prompt use of the emergency
listing authority under section 4(b)(7).
We have been reviewing and will
continue to review, at least annually,
the status of every candidate, whether or
not we have received a petition to list
it. Thus, the CNOR and accompanying
species assessment forms constitute the
Service’s annual finding on the status of
petitioned species pursuant to section
4(b)(3)(C)(i).
A number of court decisions have
elaborated on the nature and specificity
of information that must be considered
in making and describing the findings in
the CNOR. The previous CNOR, which
was published on November 9, 2009
(74 FR 57804), describes these court
decisions in further detail. As with
previous CNORs, we continue to
incorporate information of the nature
and specificity required by the courts.
For example, we include a description
of the reasons why the listing of every
petitioned candidate species is both
warranted and precluded at this time.
We make our determinations of
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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 (see below).
Regional priorities can also be discerned
from Table 1, which includes the lead
region and the LPN for each species.
Our preclusion determinations are
further based upon our budget for listing
activities for unlisted species only, and
we explain the priority system and why
the work we have accomplished does
preclude action on listing candidate
species.
Pursuant to section 4(b)(3)(C)(ii) and
the Administrative Procedure Act (5
U.S.C. 551 et seq.), any party with
standing may challenge the merits of
any not-warranted or warranted-butprecluded petition finding incorporated
in this CNOR. The analysis included
herein, together with the administrative
record for the decision at issue
(particularly the supporting species
assessment form), will provide an
adequate basis for a court to review the
petition finding.
Nothing in this document or any of
our policies should be construed as in
any way modifying the Act’s
requirement that we make a resubmitted
12-month petition finding for each
petitioned candidate within 1 year of
the date of publication of this CNOR. If
we fail to make any such finding on a
timely basis, whether through
publication of a new CNOR or some
other form of notice, any party with
standing may seek judicial review.
In this CNOR, we continue to address
the concerns of the courts by including
specific information in our discussion
on preclusion (see below). In preparing
this CNOR, we reviewed the current
status of, and threats to, the 166
candidates and 5 listed species for
which we have received a petition and
for which we have found listing or
reclassification from threatened to
endangered to be warranted but
precluded. We also reviewed the current
status of, and threats to, the Canada lynx
in New Mexico for which we received
a petition to add that State to the listed
range. We find that the immediate
issuance of a proposed rule and timely
promulgation of a final rule for each of
these species has been, for the preceding
months, and continues to be, precluded
by higher priority listing actions.
Additional information that is the basis
for this finding is found in the species
assessments and our administrative
record for each species.
Our review included updating the
status of, and threats to, petitioned
candidate or listed species for which we
published findings, pursuant to section
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4(b)(3)(B), in the previous CNOR. We
have incorporated new information we
gathered since the prior finding and, as
a result of this review, we are making
continued warranted-but-precluded
12-month findings on the petitions for
these species.
The immediate publication of
proposed rules to list these species was
precluded by our work on higher
priority listing actions, listed below,
during the period from October 1, 2009,
through September 30, 2010. We will
continue to monitor the status of all
candidate species, including petitioned
species, as new information becomes
available to determine if a change in
status is warranted, including the need
to emergency-list a species under
section 4(b)(7) of the Act.
In addition to identifying petitioned
candidate species in Table 1 below, we
also present brief summaries of why
each of these candidates warrants
listing. More complete information,
including references, is found in the
species assessment forms. You may
obtain a copy of these forms from the
Regional Office having the lead for the
species, or from the Fish and Wildlife
Service’s Internet Web site: https://
ecos.fws.gov/tess_public/pub/Species
Report.do?listingType=C&mapstatus=1.
As described above, under section 4 of
the Act we may identify and propose
species for listing based on the factors
identified in section 4(a)(1), and section
4 also provides a mechanism for the
public to petition us to add a species to
the lists of threatened species or
endangered species under the Act.
Below we describe the actions that
continue to preclude the immediate
proposal and final promulgation of a
regulation implementing each of the
petitioned actions for which we have
made a warranted-but-precluded
finding, and we describe the
expeditious progress we are making to
add qualified species to, and remove
species from, the lists of endangered or
threatened species.
Preclusion and Expeditious Progress
Preclusion is a function of the listing
priority of a species in relation to the
resources that are available and the cost
and relative priority of 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 listing
proposal regulation or whether
promulgation of such a proposal is
precluded by higher priority listing
actions.
The resources available for listing
actions are determined through the
annual Congressional appropriations
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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 ‘‘resubmitted’’
petition findings on prior warrantedbut-precluded petition findings as
required under section 4(b)(3)(C)(i) of
the Act; critical habitat petition
findings; proposed and final rules
designating critical habitat; and
litigation-related, administrative, and
program-management functions
(including preparing and allocating
budgets, responding to Congressional
and public inquiries, and conducting
public outreach regarding listing and
critical habitat). The work involved in
preparing various listing documents can
be extensive, and may include, but is
not limited to: Gathering and assessing
the best scientific and commercial data
available and conducting analyses used
as the basis for our decisions; writing
and publishing documents; and
obtaining, reviewing, and evaluating
public comments and peer-review
comments on proposed rules and
incorporating relevant information into
final rules. The number of listing
actions that we can undertake in a given
year also is influenced by the
complexity of those listing actions; that
is, more complex actions generally are
more costly. The median cost for
preparing and publishing a 90-day
finding is $39,276; for a 12-month
finding, $100,690; for a proposed rule
with critical habitat, $345,000; and for
a final listing rule with critical habitat,
the median cost is $305,000.
We cannot spend more than is
appropriated for the Listing Program
without violating the Anti-Deficiency
Act (see 31 U.S.C. 1341(a)(1)(A)). In
addition, in FY 1998 and for each fiscal
year since then, Congress has placed a
statutory cap on funds which may be
expended for the Listing Program, equal
to the amount expressly appropriated
for that purpose in that fiscal year. This
cap was designed to prevent funds
appropriated for other functions under
the Act (for example, recovery funds for
removing species from the Lists), or for
other Service programs, from being used
for Listing Program actions (see House
Report 105–163, 105th Congress, 1st
Session, July 1, 1997).
Since FY 2002, the Service’s budget
has included a critical habitat subcap to
ensure that some funds are available for
other work in the Listing Program (‘‘The
critical habitat designation subcap will
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ensure that some funding is available to
address other listing activities’’ (H.R. 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 court-mandated
designations of critical habitat, and
consequently none of the critical habitat
subcap funds have been available for
other listing activities. In FY 2007, we
were able to use some of the critical
habitat subcap funds to fund proposed
listing determinations for high-priority
candidate species. In FY 2009, while we
were unable to use any of the critical
habitat subcap funds to fund proposed
listing determinations, we did use some
of this money to fund the critical habitat
portion of some proposed listing
determinations so that the proposed
listing determination and proposed
critical habitat designation could be
combined into one rule, thereby being
more efficient in our work. In FY 2010,
we are using some of the critical habitat
subcap funds to fund listing actions
with statutory deadlines.
We 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. Through the
listing cap, the critical habitat subcap,
and the amount of funds needed to
address court-mandated critical habitat
designations, Congress and the courts
have in effect determined the amount of
money available for other listing
activities nationwide. Therefore, the
funds in the listing cap, other than those
needed to address court-mandated
critical habitat for already listed species,
represent the resources we must take
into consideration when we make our
determinations of preclusion and
expeditious progress.
Congress identified the availability of
resources as the only basis for deferring
the initiation of a rulemaking that is
warranted. The Conference Report
accompanying Public Law 97–304,
which established the current statutory
deadlines and the warranted-butprecluded finding, states that the
amendments 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.’’
Although that statement appeared to
refer specifically to the ‘‘to the
maximum extent practicable’’ limitation
on the 90-day deadline for making a
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‘‘substantial information’’ finding, that
finding is made at the point when the
Service is deciding whether or not to
commence a status review that will
determine the degree of threats facing
the species, and therefore the analysis
underlying the statement is more
relevant to the use of the warranted-butprecluded finding, which is made when
the Service has already determined the
degree of threats facing the species and
is deciding whether or not to commence
a rulemaking.
In FY 2010, $10,471,000 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). Therefore, a proposed
listing is precluded if pending proposals
with higher priority will require
expenditure of at least $10,471,000, and
expeditious progress is the amount of
work that can be achieved with
$10,471,000. Since court orders
requiring critical habitat work will not
require use of all of the funds within the
critical habitat subcap, we are using
$1,114,417 of our critical habitat subcap
funds in order to work on as many of
our required petition findings and
listing determinations as possible. This
brings the total amount of funds we
have for listing action in FY 2010 to
$11,585,417.
The $11,585,417 is being used to fund
work in the following categories:
Compliance with court orders and
court-approved settlement agreements
requiring that petition findings or listing
determinations be completed by a
specific date; section 4 (of the Act)
listing actions with absolute statutory
deadlines; essential litigation-related,
administrative, and listing programmanagement functions; and highpriority listing actions for some of our
candidate species. In 2009, the
responsibility for listing foreign species
under the Act was transferred from the
Division of Scientific Authority,
International Affairs Program, to the
Endangered Species Program. Therefore,
starting in FY 2010, a portion of our
funding is being used to work on the
actions described above as they apply to
listing actions for foreign species. This
has the potential to further reduce
funding available for domestic listing
actions. Although there are currently no
foreign species issues included in our
high-priority listing actions at this time,
many actions have statutory or courtapproved settlement deadlines, thus
increasing their priority. The budget
allocations for each specific listing
action are identified in the Service’s FY
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2010 Allocation Table (part of our
administrative record).
Based on our September 21, 1983,
guidance for assigning an LPN for each
candidate species (48 FR 43098), we
have a significant number of species
with an LPN of 2. Under this guidance,
we assign each candidate an LPN of 1
to 12, depending on the magnitude of
threats (high or moderate to low),
immediacy of threats (imminent or
nonimminent), and taxonomic status of
the species (in order of priority:
Monotypic genus (a species that is the
sole member of a genus), species, or part
of a species (subspecies, distinct
population segment, or significant
portion of the range)). The lower the
listing priority number, the higher the
listing priority (that is, a species with an
LPN of 1 would have the highest listing
priority).
Because of the large number of highpriority species, we have further ranked
the candidate species with an LPN of 2
by using the following extinction-risk
type criteria: International Union for the
Conservation of Nature and Natural
Resources (IUCN) Red list status/rank,
Heritage rank (provided by
NatureServe), Heritage threat rank
(provided by NatureServe), and species
currently with fewer than 50
individuals, or 4 or fewer populations.
Those species with the highest IUCN
rank (critically endangered), the highest
Heritage rank (G1), the highest Heritage
threat rank (substantial, imminent
threats), and currently with fewer than
50 individuals, or fewer than 4
populations, originally comprised a
group of approximately 40 candidate
species (‘‘Top 40’’). These 40 candidate
species have had the highest priority to
receive funding to work on a proposed
listing determination. As we work
through proposed and final listing rules
for those 40 candidates, we apply the
ranking criteria to the next group of
candidates with LPNs of 2 and 3 to
determine the next set of highest
priority candidate species. 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. However, for efficiency
reasons, we may choose to work on a
proposed rule to reclassify a species to
endangered if we can combine this with
work that is subject to a courtdetermined deadline.
With our workload so much bigger
than the amount of funds we have to
accomplish it, it is important that we be
as efficient as possible in our listing
process. Therefore, as we work on
proposed rules for the highest priority
species in the next several years, we are
preparing multi-species proposals when
appropriate, and these may include
species with lower priority if they
overlap geographically or have the same
threats as a species with an LPN of 2.
In addition, we take into consideration
the availability of staff resources when
we determine which high-priority
69231
species will receive funding to
minimize the amount of time and
resources required to complete each
listing action.
Based on these prioritization factors,
we continue to find that proposals to list
the petitioned candidate species
included in Table 1 are all warranted
but precluded.
As explained above, a determination
that listing is warranted but precluded
must also demonstrate that expeditious
progress is being made to add and
remove qualified species to and from
the Lists of Endangered and Threatened
Wildlife and Plants. As with our
‘‘precluded’’ finding, the evaluation of
whether progress in adding qualified
species to the Lists has been expeditious
is a function of the resources available
for listing and the competing demands
for those funds. Given the limited
resources available for listing, we find
that we made expeditious progress in
FY 2010 in the Listing Program.
(Although we do not discuss it in detail
here, we are making expeditious
progress in removing species from the
list under the Recovery program in light
of the resource available for delisting,
which is funded by a separate line item
in the budget of the Endangered Species
Program. During FY 2010, we have
completed two proposed delisting rules
and two final delisting rules.) Progress
in adding qualified species to the list
included preparing and publishing the
following determinations:
FY 2010 COMPLETED LISTING ACTIONS
Publication date
Title
Actions
10/08/2009 ...................
Listing Lepidium papilliferum (Slickspot Peppergrass)
as a Threatened Species Throughout Its Range.
90-day Finding on a Petition To List the American
Dipper in the Black Hills of South Dakota as Threatened or Endangered.
Status Review of Arctic Grayling (Thymallus arcticus)
in the Upper Missouri River System.
Listing the British Columbia Distinct Population Segment of the Queen Charlotte Goshawk Under the
Endangered Species Act: Proposed rule.
Listing the Salmon-Crested Cockatoo as Threatened
Throughout Its Range with Special Rule.
Status
Review
of
Gunnison
sage-grouse
(Centrocercus minimus).
12-Month Finding on a Petition to List the Black-tailed
Prairie Dog as Threatened or Endangered.
90-Day Finding on a Petition to List Sprague’s Pipit as
Threatened or Endangered.
90-Day Finding on Petitions To List Nine Species of
Mussels From Texas as Threatened or Endangered
With Critical Habitat.
Partial 90-Day Finding on a Petition to List 475 Species in the Southwestern United States as Threatened or Endangered With Critical Habitat Critical
Habitat.
Final Listing Threatened ..................
74 FR 52013–52064.
Notice of 90-day Petition Finding,
Not substantial.
74 FR 55177–55180.
Notice of Intent to Conduct Status
Review for Listing Decision.
Proposed Listing Threatened ..........
74 FR 55524–55525.
74 FR 56757–56770.
Proposed Listing Threatened ..........
74 FR 56770–56791.
Notice of Intent to Conduct Status
Review for Listing Decision.
Notice of 12-month petition finding,
Not warranted.
Notice of 90-day Petition Finding,
Substantial.
Notice of 90-day Petition Finding,
Substantial.
74 FR 61100–61102.
Notice of 90-day Petition Finding,
Not substantial and Substantial.
74 FR 66865–66905.
10/27/2009 ...................
10/28/2009 ...................
11/03/2009 ...................
11/03/2009 ...................
11/23/2009 ...................
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74 FR 63343–63366.
74 FR 63337–63343.
74 FR 66260–66271.
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FY 2010 COMPLETED LISTING ACTIONS—Continued
Publication date
Title
Actions
12/17/2009 ...................
12-month Finding on a Petition To Change the Final
Listing of the Distinct Population Segment of the
Canada Lynx To Include New Mexico.
Listing Foreign Bird Species in Peru and Bolivia as
Endangered Throughout Their Range.
Listing Six Foreign Birds as Endangered Throughout
Their Range.
Withdrawal of Proposed Rule to List Cook’s Petrel .....
Final Rule to List the Galapagos Petrel and Heinroth’s
Shearwater as Threatened Throughout Their
Ranges.
Initiation of Status Review for Agave eggersiana and
Solanum conocarpum.
12-month Finding on a Petition to List the American
Pika as Threatened or Endangered.
12-Month Finding on a Petition To List the Sonoran
Desert Population of the Bald Eagle as a Threatened or Endangered Distinct Population Segment.
Withdrawal of Proposed Rule To List the Southwestern Washington/Columbia River Distinct Population Segment of Coastal Cutthroat Trout
(Oncorhynchus clarki clarki) as Threatened.
90-Day Finding on a Petition to List the Berry Cave
salamander as Endangered.
90-Day Finding on a Petition to List the Southern
Hickorynut Mussel (Obovaria jacksoniana) as Endangered or Threatened.
90-Day Finding on a Petition to List the Striped Newt
as Threatened.
12-Month Findings for Petitions to List the Greater
Sage-Grouse (Centrocercus urophasianus) as
Threatened or Endangered.
12-Month Finding on a Petition to List the Tucson
Shovel-Nosed
Snake
(Chionactis
occipitalis
klauberi) as Threatened or Endangered with Critical
Habitat.
90-Day Finding on a Petition To List Thorne’s
Hairstreak Butterfly as threatened or Endangered.
12-month Finding on a Petition To List the Mountain
Whitefish in the Big Lost River, Idaho, as Endangered or Threatened.
90-Day Finding on a Petition to List a Stonefly
(Isoperla jewetti) and a Mayfly (Fallceon eatoni) as
Threatened or Endangered with Critical Habitat.
12-Month Finding on a Petition to Reclassify the Delta
Smelt From Threatened to Endangered Throughout
Its Range.
Determination of Endangered Status for 48 Species
on Kauai and Designation of Critical Habitat.
Initiation of Status Review of the North American Wolverine in the Contiguous United States.
12-Month Finding on a Petition to List the Wyoming
Pocket Gopher as Endangered or Threatened with
Critical Habitat.
90-Day Finding on a Petition to List a Distinct Population Segment of the Fisher in Its United States
Northern Rocky Mountain Range as Endangered or
Threatened with Critical Habitat.
Initiation of Status Review for Sacramento splittail
(Pogonichthys macrolepidotus).
90-Day Finding on a Petition to List the Harlequin Butterfly as Endangered.
12-Month Finding on a Petition to List Susan’s Pursemaking Caddisfly (Ochrotrichia susanae) as Threatened or Endangered.
90-day Finding on a Petition to List the Mohave
Ground Squirrel as Endangered with Critical Habitat.
90-Day Finding on a Petition to List Hermes Copper
Butterfly as Threatened or Endangered.
90-Day Finding on a Petition To List Castanea pumila
var. ozarkensis.
Notice of 12-month petition finding,
Warranted but precluded.
74 FR 66937–66950.
Proposed Listing Endangered .........
75 FR 605–649.
Proposed Listing Endangered .........
75 FR 286–310.
Proposed rule, withdrawal ...............
Final Listing Threatened ..................
75 FR 310–316.
75 FR 235–250.
Notice of Intent to Conduct Status
Review for Listing Decision.
Notice of 12-month petition finding,
Not warranted.
Notice of 12-month petition finding,
Not warranted.
75 FR 3190–3191.
Withdrawal of Proposed Rule to List
75 FR 8621–8644.
Notice of 90-day Petition Finding,
Substantial.
Notice of 90-day Petition Finding,
Not substantial.
75 FR 13068–13071.
Notice of 90-day Petition Finding,
Substantial.
Notice of 12-month petition finding,
Warranted but precluded.
75 FR 13720–13726.
Notice of 12-month petition finding,
Warranted but precluded.
75 FR 16050–16065.
Notice of 90-day Petition Finding,
Substantial.
Notice of 12-month petition finding,
Not warranted.
75 FR 17062–17070.
Notice of 90-day Petition Finding,
Not substantial.
75 FR 17363–17367.
Notice of 12-month petition finding,
Warranted but precluded.
75 FR 17667–17680.
Final Listing Endangered .................
75 FR 18959–19165.
Notice of Initiation of Status Review
for Listing Decision.
Notice of 12-month petition finding,
Not warranted.
75 FR 19591–19592.
Notice of 90-day Petition Finding,
Substantial.
75 FR 19925–19935.
Notice of Initiation of Status Review
for Listing Decision.
Notice of 90-day Petition Finding,
Substantial.
Notice of 12-month petition finding,
Not warranted.
75 FR 20547–20548.
Notice of 90-day Petition Finding,
Substantial.
Notice of 90-day Petition Finding,
Substantial.
Notice of 90-day Petition Finding,
Substantial.
75 FR 22063–22070.
1/05/2010 .....................
1/05/2010 .....................
1/05/2010 .....................
1/05/2010 .....................
1/20/2010 .....................
2/09/2010 .....................
2/25/2010 .....................
2/25/2010 .....................
3/18/2010 .....................
3/23/2010 .....................
3/23/2010 .....................
3/23/2010 .....................
3/31/2010 .....................
4/5/2010 .......................
4/6/2010 .......................
4/6/2010 .......................
4/7/2010 .......................
4/13/2010 .....................
4/15/2010 .....................
4/15/2010 .....................
4/16/2010 .....................
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5/4/2010 .......................
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75 FR 6437–6471.
75 FR 8601–8621.
75 FR 13717–13720.
75 FR 13910–14014.
75 FR 17352–17363.
75 FR 19592–19607.
75 FR 21568–21571.
75 FR 22012–22025.
75 FR 23654–23663.
75 FR 30313–30318.
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FY 2010 COMPLETED LISTING ACTIONS—Continued
Publication date
Title
Actions
6/1/2010 .......................
12-month Finding on a Petition to List the White-tailed
Prairie Dog as Endangered or Threatened.
90-Day Finding on a Petition To List van Rossem’s
Gull-billed Tern as Endangered or Threatened.
90-Day Finding on Five Petitions to List Seven Species of Hawaiian Yellow-faced Bees as Endangered.
12-Month Finding on a Petition to List the Least Chub
as Threatened or Endangered.
90-Day Finding on a Petition to List the Honduran
Emerald Hummingbird as Endangered.
Listing Ipomopsis polyantha (Pagosa Skyrocket) as
Endangered Throughout Its Range, and Listing
Penstemon debilis (Parachute Beardtongue) and
Phacelia submutica (DeBeque Phacelia) as Threatened Throughout Their Range.
Listing the Flying Earwig Hawaiian Damselfly and Pacific Hawaiian Damselfly As Endangered Throughout Their Ranges.
Listing the Cumberland Darter, Rush Darter,
Yellowcheek Darter, Chucky Madtom, and Laurel
Dace as Endangered Throughout Their Ranges.
Listing the Mountain Plover as Threatened ..................
Notice of 12-month petition finding,
Not warranted.
Notice of 90-day Petition Finding,
Substantial.
Notice of 90-day Petition Finding,
Substantial.
Notice of 12-month petition finding,
Warranted but precluded.
Notice of 90-day Petition Finding,
Substantial.
Proposed Listing Endangered .........
Proposed Listing Threatened
75 FR 30338–30363.
Final Listing Endangered .................
75 FR 35990–36012.
Proposed Listing Endangered .........
75 FR 36035–36057.
Reinstatement of Proposed Listing
Threatened.
Notice of 90-day Petition Finding,
Substantial.
75 FR 37353–37358.
Notice of 12-month petition finding,
Not warranted.
Notice of 90-day Petition Finding,
Substantial.
75 FR 42040–42054.
Final Listing Endangered .................
75 FR 43844–43853.
Final Listing Endangered .................
75 FR 43853–43864.
Final Listing Threatened ..................
75 FR 45497–45527.
Notice of 90-day Petition Finding,
Substantial.
75 FR 46894–46898.
Notice of 90-day Petition Finding,
Substantial.
Final Listing Endangered .................
75 FR 48294–48298.
6/9/2010 .......................
6/16/2010 .....................
6/22/2010 .....................
6/23/2010 .....................
6/23/2010 .....................
6/24/2010 .....................
6/24/2010 .....................
6/29/2010 .....................
7/20/2010 .....................
7/20/2010 .....................
7/20/2010 .....................
7/27/2010 .....................
7/27/2010 .....................
8/3/2010 .......................
8/4/2010 .......................
8/10/2010 .....................
8/17/2010 .....................
8/17/2010 .....................
8/24/2010 .....................
9/1/2010 .......................
9/8/2010 .......................
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90-Day Finding on a Petition to List Pinus albicaulis
(Whitebark Pine) as Endangered or Threatened
with Critical Habitat.
12-Month Finding on a Petition to List the Amargosa
Toad as Threatened or Endangered.
90-Day Finding on a Petition to List the Giant Palouse
Earthworm (Driloleirus americanus) as Threatened
or Endangered.
Determination on Listing the Black-Breasted Puffleg
as Endangered Throughout its Range; Final Rule.
Final Rule to List the Medium Tree-Finch
(Camarhynchus pauper) as Endangered Throughout Its Range.
Determination of Threatened Status for Five Penguin
Species.
90-Day Finding on a Petition To List the Mexican
Gray Wolf as an Endangered Subspecies With Critical Habitat.
90-Day Finding on a Petition to List Arctostaphylos
franciscana as Endangered with Critical Habitat.
Listing Three Foreign Bird Species from Latin America
and the Caribbean as Endangered Throughout
Their Range.
90-Day Finding on a Petition to List Brian Head
Mountainsnail as Endangered or Threatened with
Critical Habitat.
90-Day Finding on a Petition to List the Oklahoma
Grass Pink Orchid as Endangered or Threatened.
12-Month Finding on a Petition to List the White-Sided
Jackrabbit as Threatened or Endangered.
Proposed Rule To List the Ozark Hellbender Salamander as Endangered.
Revised 12-Month Finding to List the Upper Missouri
River Distinct Population Segment of Arctic Grayling
as Endangered or Threatened.
12-Month Finding on a Petition to List the Jemez
Mountains Salamander (Plethodon neomexicanus)
as Endangered or Threatened with Critical Habitat.
12-Month Finding on a Petition to List Sprague’s Pipit
as Endangered or Threatened Throughout Its
Range.
12-Month Finding on a Petition to List Agave
eggersiana (no common name) as Endangered.
Determination of Endangered Status for the African
Penguin.
Determination for the Gunnison Sage-grouse as a
Threatened or Endangered Species.
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FR pages
75 FR 32728–32734.
75 FR 34077–34088.
75 FR 35398–35424.
75 FR 35746–35751.
75 FR 35721–35746.
75 FR 42033–42040.
75 FR 42059–42066.
75 FR 50813–50842.
Notice of 90-day Petition Finding,
Not substantial.
75 FR 50739–50742.
Notice of 90-day Petition Finding,
Substantial.
Notice of 12-month petition finding,
Not warranted.
Proposed Listing Endangered .........
75 FR 51969–51974.
75 FR 53615–53629.
75 FR 54561–54579.
Notice of 12-month petition finding,
Warranted but precluded.
75 FR 54707–54753.
Notice of 12-month petition finding,
Warranted but precluded.
75 FR 54822–54845.
Notice of 12-month petition finding,
Warranted but precluded.
75 FR 56028–56050.
Notice of 12-month petition finding,
Warranted but precluded.
Final Listing Endangered .................
75 FR 57720–57734.
Notice of 12-month petition finding,
Warranted but precluded.
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75 FR 59645–59656.
75 FR 59803–59863.
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FY 2010 COMPLETED LISTING ACTIONS—Continued
Publication date
Title
Actions
9/30/2010 .....................
12-Month Finding on a Petition to List the Pygmy
Rabbit as Endangered or Threatened.
Notice of 12-month petition finding,
Not warranted.
Our expeditious progress also
included work on listing actions that we
funded in FY 2010 but have not yet
been completed to date. These actions
are listed below. Actions in the top
section of the table are being conducted
under a deadline set by a court. Actions
in the middle section of the table are
being conducted to meet statutory
timelines, that is, timelines required
under the Act. Actions in the bottom
section of the table are high-priority
listing actions. These actions include
work primarily on species with an LPN
of 2, and, as discussed above, selection
of these species is partially based on
available staff resources, and when
appropriate, include species with a
FR pages
75 FR 60515–60561.
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, compared to preparing separate
proposed rules for each of them in the
future.
ACTIONS FUNDED IN FY 2010 BUT NOT YET COMPLETED
jlentini on DSKJ8SOYB1PROD with PROPOSALS3
Species
Action
Actions Subject to Court Order/Settlement Agreement
6 Birds from Eurasia .....................................................................................................................
Flat-tailed horned lizard ................................................................................................................
Mountain plover 3 ..........................................................................................................................
6 Birds from Peru .........................................................................................................................
Sacramento splittail ......................................................................................................................
Pacific walrus ................................................................................................................................
Wolverine ......................................................................................................................................
Solanum conocarpum ...................................................................................................................
Desert tortoise—Sonoran population ...........................................................................................
Thorne’s Hairstreak butterfly 3 ......................................................................................................
Hermes copper butterfly 3 .............................................................................................................
Actions with Statutory Deadlines
Casey’s june beetle ......................................................................................................................
Georgia pigtoe, interrupted rocksnail, and rough hornsnail .........................................................
7 Bird species from Brazil ............................................................................................................
Southern rockhopper penguin—Campbell Plateau population ....................................................
5 Bird species from Colombia and Ecuador ................................................................................
Queen Charlotte goshawk ............................................................................................................
5 species southeast fish (Cumberland darter, rush darter, yellowcheek darter, chucky
madtom, and laurel dace).
Salmon crested cockatoo .............................................................................................................
CA golden trout ............................................................................................................................
Black-footed albatross ..................................................................................................................
Mount Charleston blue butterfly ...................................................................................................
Mojave fringe-toed lizard 1 ............................................................................................................
Kokanee—Lake Sammamish population 1 ...................................................................................
Cactus ferruginous pygmy-owl 1 ...................................................................................................
Northern leopard frog ...................................................................................................................
Tehachapi slender salamander ....................................................................................................
Coqui Llanero ...............................................................................................................................
Dusky tree vole .............................................................................................................................
3 MT invertebrates (mist forestfly (Lednia tumana), Oreohelix sp. 3, Oreohelix sp. 31) from
206 species petition.
5 UT plants (Astragalus hamiltonii, Eriogonum soredium, Lepidium ostleri, Penstemon
flowersii, Trifolium friscanum) from 206 species petition.
2 CO plants (Astragalus microcymbus, Astragalus schmolliae) from 206 species petition ........
5 WY plants (Abronia ammophila, Agrostis rossiae, Astragalus proimanthus, Boechere
(Arabis) pusilla, Penstemon gibbensii) from 206 species petition.
Leatherside chub (from 206 species petition) ..............................................................................
Frigid ambersnail (from 206 species petition) ..............................................................................
Gopher tortoise—eastern population ...........................................................................................
Wrights marsh thistle ....................................................................................................................
67 of 475 southwest species ........................................................................................................
Grand Canyon scorpion (from 475 species petition) ...................................................................
Anacroneuria wipukupa (a stonefly from 475 species petition) ...................................................
Rattlesnake-master borer moth (from 475 species petition) ........................................................
3 Texas moths (Ursia furtiva, Sphingicampa blanchardi, Agapema galbina) (from 475 species
petition).
2 Texas shiners (Cyprinella sp., Cyprinella lepida) (from 475 species petition) .........................
3 South Arizona plants (Erigeron piscaticus, Astragalus hypoxylus, Amoreuxia gonzalezii)
(from 475 species petition).
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Final listing determination.
Final listing determination.
Final listing determination.
Proposed listing determination.
12-month petition finding.
12-month petition finding.
12-month petition finding.
12-month petition finding.
12-month petition finding.
12-month petition finding.
12-month petition finding.
Final
Final
Final
Final
Final
Final
Final
listing
listing
listing
listing
listing
listing
listing
determination.
determination.
determination.
determination.
determination.
determination.
determination.
Proposed listing determination.
12-month petition finding.
12-month petition finding.
12-month petition finding.
12-month petition finding.
12-month petition finding.
12-month petition finding.
12-month petition finding.
12-month petition finding.
12-month petition finding.
12-month petition finding.
12-month petition finding.
12-month petition finding.
12-month petition finding.
12-month petition finding.
12-month
12-month
12-month
12-month
12-month
12-month
12-month
12-month
12-month
petition
petition
petition
petition
petition
petition
petition
petition
petition
finding.
finding.
finding.
finding.
finding.
finding.
finding.
finding.
finding.
12-month petition finding.
12-month petition finding.
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69235
ACTIONS FUNDED IN FY 2010 BUT NOT YET COMPLETED—Continued
Species
Action
5 Central Texas mussel species (3 from 475 species petition) ...................................................
14 parrots (foreign species) .........................................................................................................
Berry Cave salamander 1 .............................................................................................................
Striped Newt 1 ...............................................................................................................................
Fisher—Northern Rocky Mountain Range 1 .................................................................................
Mohave Ground Squirrel 1 ............................................................................................................
Puerto Rico Harlequin Butterfly ....................................................................................................
Western gull-billed tern .................................................................................................................
Ozark chinquapin (Castanea pumila var. ozarkensis) .................................................................
HI yellow-faced bees ....................................................................................................................
Giant Palouse earthworm .............................................................................................................
Whitebark pine ..............................................................................................................................
OK grass pink (Calopogon oklahomensis) 1 ................................................................................
Southeastern pop snowy plover & wintering pop. of piping plover 1 ...........................................
Eagle Lake trout 1 .........................................................................................................................
Smooth-billed ani 1 ........................................................................................................................
Bay Springs salamander 1 ............................................................................................................
32 species of snails and slugs 1 ...................................................................................................
42 snail species (Nevada & Utah) ...............................................................................................
Red knot roselaari subspecies .....................................................................................................
Peary caribou ...............................................................................................................................
Plains bison ..................................................................................................................................
Spring Mountains checkerspot butterfly .......................................................................................
Spring pygmy sunfish ...................................................................................................................
Bay skipper ...................................................................................................................................
Unsilvered fritillary ........................................................................................................................
Texas kangaroo rat ......................................................................................................................
Spot-tailed earless lizard ..............................................................................................................
Eastern small-footed bat ..............................................................................................................
Northern long-eared bat ...............................................................................................................
Prairie chub ..................................................................................................................................
10 species of Great Basin butterfly ..............................................................................................
6 sand dune (scarab) beetles ......................................................................................................
Golden-winged warbler .................................................................................................................
Sand-verbena moth ......................................................................................................................
404 Southeast species .................................................................................................................
High-Priority Listing Actions 3
19 Oahu candidate species 2 (16 plants, 3 damselflies) (15 with LPN = 2, 3 with LPN = 3, 1
with LPN =9).
19 Maui-Nui candidate species 2 (16 plants, 3 tree snails) (14 with LPN = 2, 2 with LPN = 3,
3 with LPN = 8).
Dune sagebrush lizard (formerly Sand dune lizard) 3 (LPN = 2) .................................................
2 Arizona springsnails 2 (Pyrgulopsis bernadina (LPN = 2), Pyrgulopsis trivialis (LPN = 2)) ......
New Mexico springsnail 2 (Pyrgulopsis chupaderae (LPN = 2)) ..................................................
2 mussels 2 (rayed bean (LPN = 2), snuffbox No LPN) ...............................................................
2 mussels 2 (sheepnose (LPN = 2), spectaclecase (LPN = 4)).
Altamaha spinymussel 2 (LPN = 2) ..............................................................................................
8 southeast mussels (southern kidneyshell (LPN = 2), round ebonyshell (LPN = 2), Alabama
pearlshell (LPN = 2), southern sandshell (LPN = 5), fuzzy pigtoe (LPN = 5), Choctaw bean
(LPN = 5), narrow pigtoe (LPN = 5), and tapered pigtoe (LPN = 11)).
12-month petition finding.
12-month petition finding.
12-month petition finding.
12-month petition finding.
12-month petition finding.
12-month petition finding.
12-month petition finding.
12-month petition finding.
12-month petition finding.
12-month petition finding.
12-month petition finding.
12-month petition finding.
12-month petition finding.
90-day petition finding.
90-day petition finding.
90-day petition finding.
90-day petition finding.
90-day petition finding.
90-day petition finding.
90-day petition finding.
90-day petition finding.
90-day petition finding.
90-day petition finding.
90-day petition finding.
90-day petition finding.
90-day petition finding.
90-day petition finding.
90-day petition finding.
90-day petition finding.
90-day petition finding.
90-day petition finding.
90-day petition finding.
90-day petition finding.
90-day petition finding.
90-day petition finding.
90-day petition finding.
Proposed listing.
Proposed listing.
Proposed
Proposed
Proposed
Proposed
Proposed
Proposed
Proposed
listing.
listing.
listing.
listing.
listing.
listing.
listing.
1 Funds
for listing actions for these species were provided in previous FYs.
funds for these high-priority listing actions were provided in FY 2008 or 2009, due to the complexity of these actions and competing
priorities, these actions are still being developed.
3 Partially funded with FY 2010 funds; also will be funded with FY 2011 funds.
jlentini on DSKJ8SOYB1PROD with PROPOSALS3
2 Although
We also funded work on resubmitted
petitions findings for 162 candidate
species (species petitioned prior to the
last CNOR). We did not include new
information in our resubmitted petition
finding for the Columbia Basin
population of the greater sage-grouse in
this notice, as the significance of the
Columbia Basin DPS to the greater sagegrouse will require further review and
we will update our finding at a later
date (see 75 FR 13909; March 23, 2010).
We also did not include new
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information in our resubmitted petition
findings for the 43 candidate species for
which we are preparing proposed listing
determinations; see summaries below
regarding publication of these
determinations (these species will
remain on the candidate list until a
proposed listing rule is published). We
also funded a revised 12-month petition
finding for the candidate species that we
are removing from candidate status,
which is being published as part of this
CNOR (see Candidate Removals).
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Because the majority of these species
were already candidate species prior to
our receipt of a petition to list them, we
had already assessed their status using
funds from our Candidate Conservation
Program. We also continue to monitor
the status of these species through our
Candidate Conservation Program. The
cost of updating the species assessment
forms and publishing the joint
publication of the CNOR and
resubmitted petition findings is shared
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jlentini on DSKJ8SOYB1PROD with PROPOSALS3
between the Listing Program and the
Candidate Conservation Program.
During FY 2010, we also funded work
on resubmitted petition findings for
uplisting six listed species, for which
petitions were previously received.
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
processes or achieve economies of scale,
such as by batching related actions
together. Given our limited budget for
implementing section 4 of the Act, the
actions described above collectively
constitute expeditious progress.
Although we have not been able to
resolve the listing status of many of the
candidates, several programs in the
Service contribute to the conservation of
these species. In particular, the
Candidate Conservation program, which
is separately budgeted, focuses on
providing technical expertise for
developing conservation strategies and
agreements to guide voluntary on-theground conservation work for candidate
and other at-risk species. The main goal
of this program is to address the threats
facing candidate species. Through this
program, we work with our partners
(other Federal agencies, State agencies,
Tribes, local governments, private
landowners, and private conservation
organizations) to address the threats to
candidate species and other species atrisk. We are currently working with our
partners to implement voluntary
conservation agreements for more than
140 species covering 5 million acres of
habitat. In some instances, the sustained
implementation of strategically
designed conservation efforts
culminates in making listing
unnecessary for species that are
candidates for listing or for which
listing has been proposed.
Findings for Petitioned Candidate
Species
Below are updated summaries for
petitioned candidates for which we
published findings, pursuant to section
4(b)(3)(B). We are making continued
warranted-but-precluded 12-month
findings on the petitions for these
species (for our revised 12-month
petition findings for species we are
removing from candidate status, see
summaries above under ‘‘Candidate
Removals’’).
Mammals
Florida bonneted bat (Eumops
floridanus)—The following summary is
based on information in our files. No
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new information was presented in the
petition received on January 29, 2010.
Endemic to south Florida, this species
has been found at 12 locations, 5 on
private land and 7 on public land. The
entire population may number less than
a few hundred individuals. Results from
a rangewide acoustical survey found a
small number of locations where calls
were recorded, and low numbers of calls
were recorded at each location. Few
active roost sites are known; all are
artificial (i.e., bat houses). Prolonged
cold temperatures in January and
February 2010 affected one active roost;
it is not clear what effect the prolonged
cold had on the species. Efforts are
under way to confirm presence at all
previously documented sites.
Occurrences are threatened by loss
and conversion of habitat to other uses
and habitat alteration (e.g., removal of
old trees with cavities, removal of
manmade structures with suitable
roosting sites); this threat is expected to
continue and increase. Although
occurrences on conservation lands are
inherently more protected than those on
private lands, habitat alteration during
management practices may affect
natural roosting sites even on
conservation lands if Florida bonneted
bats are present but undetected.
Therefore, occupied and potential
habitat on forested or wooded lands,
both private and public, continues to be
at risk. The species is vulnerable to a
wide array of natural and human
factors: Low population size, restricted
range, low fecundity, large distances
between occupied locations, and small
number of occupied locations. Such
factors may make recolonization
unlikely if any site is extirpated and
may make the species vulnerable to
extinction due to genetic drift,
inbreeding depression, extreme weather
events, and random or chance changes
to the environment. Where the species
occurs in or near human dwellings or
structures, it is at risk to persecution,
removal, and disturbance. Disturbance
from humans, either intentional or
inadvertent, can occur at any of the
occurrences of this bat on either private
or conservation lands. Disturbance of
maternity roosts is of particular concern
due to this species’ low fecundity and
small population. Pesticide applications
may be affecting its foraging base,
especially in coastal areas.
Due to its overall vulnerability,
intense hurricanes are a significant
threat; this threat is expected to
continue or increase in the future.
Intense storms can cause mortality
during the storm, exposure to predation
immediately following the storm, loss of
roost sites, impacts on foraging areas
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and insect abundance, and disruption of
the maternal period. Prolonged periods
of cold temperatures may have severe
impacts on the population and increase
risks from other threats by weakening
individuals, extirpating colonies, or
further reducing colony sizes. Although
disease is a significant threat for other
bat species, it is not known to be a
threat for the Florida bonneted bat at
this time. The protection currently
afforded the Florida bonneted bat is
limited, provides little protection to the
species’ occupied habitat, and includes
no provisions to protect suitable but
unoccupied habitat within the vicinity
of known colony sites. Overall, we find
the magnitude of threats is high due to
the severity of the threats on this
species. We find that most of the threats
are currently occurring and,
consequently, overall, threats are
imminent. Therefore, we assigned an
LPN of 2 to this species.
Pacific Sheath-tailed Bat, American
Samoa DPS (Emballonura semicaudata
semicaudata)—The following summary
is based on information contained in
our files. No new information was
provided in the petition we received on
May 11, 2004. This small bat is a
member of the Emballonuridae, an Old
World bat family that has an extensive
distribution, primarily in the tropics.
The Pacific sheath-tailed bat was once
common and widespread in Polynesia
and Micronesia and it is the only
insectivorous bat recorded from a large
part of this area. The species as a whole
(E. semicaudata) occurred on several of
the Caroline Islands (Palau, Chuuk, and
Pohnpei), Samoa (Independent and
American), the Mariana Islands (Guam
and the CNMI), Tonga, Fiji, and
Vanuatu. While populations appear to
be healthy in some locations, mainly in
the Caroline Islands, they have declined
substantially in other areas, including
Independent and American Samoa, the
Mariana Islands, Fiji, and possibly
Tonga. Scientists recognize four
subspecies: E. s. rotensis, endemic to the
Mariana Islands (Guam and the
Commonwealth of the Northern Mariana
Islands (CNMI)); E. s. sulcata, occurring
in Chuuk and Pohnpei; E. s. palauensis,
found in Palau; and E. s. semicaudata,
occurring in American and Independent
Samoa, Tonga, Fiji, and Vanuatu. The
candidate assessment form addresses
the distinct population segment (DPS) of
E. s. semicaudata that occurs in
American Samoa.
E. s. semicaudata historically
occurred in American and Independent
Samoa, Tonga, Fiji, and Vanuatu. It is
extant in Fiji and Tonga, but may be
extirpated from Vanuatu and
Independent Samoa. There is some
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concern that it is also extirpated from
American Samoa, the location of this
DPS, where surveys are currently
ongoing to ascertain its status. The
factors that led to the decline of this
subspecies and the DPS are poorly
understood; however, current threats to
this subspecies and the DPS include
habitat loss, predation by introduced
species, and its small population size
and distribution, which make the taxon
extremely vulnerable to extinction due
to typhoons and similar natural
catastrophes. Thus, the threats are high
in magnitude. The Pacific sheath-tailed
bat may also by susceptible to
disturbance to roosting caves. The LPN
for E. s. semicaudata is 3 because the
magnitude of the threats is high, the
threats are ongoing, and therefore,
imminent, and the taxon is a distinct
population segment of a subspecies.
Pacific Sheath-tailed Bat
(Emballonura semicaudata rotensis),
Guam and the Commonwealth of the
Northern Mariana Islands—The
following summary is based on
information contained in our files. No
new information was provided in the
petition we received on May 11, 2004.
This small bat is a member of the
Emballonuridae, an Old World bat
family that has an extensive
distribution, primarily in the tropics.
The Pacific sheath-tailed bat was once
common and widespread in Polynesia
and Micronesia and it is the only
insectivorous bat recorded from a large
part of this area. E. s. rotensis is
historically known from the Mariana
Islands and formerly occurred on Guam
and in the CNMI on Rota, Aguiguan,
Tinian (known from prehistoric records
only), Saipan, and possibly Anatahan
and Maug. Currently, E. s. rotensis
appears to be extirpated from all but one
island in the Mariana archipelago. The
single remaining population of this
subspecies occurs on Aguiguan, CNMI.
Threats to this subspecies have not
changed over the past year. The primary
threats to the subspecies are ongoing
habitat loss and degradation as a result
of feral goat (Capra hircus) activity on
the island of Aguiguan and the taxon’s
small population size and limited
distribution. Predation by nonnative
species and human disturbance are also
potential threats to the subspecies. The
subspecies is believed near the point
where stochastic events, such as
typhoons, are increasingly likely to
affect its continued survival. The
disappearance of the remaining
population on Aguiguan would result in
the extinction of the subspecies. Thus,
the threats are high in magnitude. The
LPN for E. s. rotensis remains at 3
because the magnitude of the threats is
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17:02 Nov 09, 2010
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high, the threats are ongoing, and
therefore, imminent, and the taxon is a
subspecies.
New England cottontail (Sylvilagus
transitionalis)—The following summary
is based on information contained in
our files and information received in
response to our notice published on
June 30, 2004, when we announced our
90-day petition finding and initiation of
a status review (69 FR 39395). We
received the petition on August 30,
2000. The New England cottontail (NEC)
is a medium-to-large sized cottontail
rabbit that may reach 1,000 grams in
weight, and is one of two species within
the genus Sylvilagus occurring in New
England. New England cottontails are
considered habitat specialists, in so far
as they are dependent upon earlysuccessional habitats typically
described as thickets. The species is the
only endemic cottontail in New
England. Historically, the NEC occurred
in seven States and ranged from
southeastern New York (east of the
Hudson River) north through the
Champlain Valley, southern Vermont,
the southern half of New Hampshire,
southern Maine, and south throughout
Massachusetts, Connecticut and Rhode
Island. The current range of the NEC has
declined substantially and occurrences
have become increasingly separated.
The species’ distribution is fragmented
into five apparently isolated
metapopulations. The area occupied by
the cottontail has contracted from
approximately 90,000 sq km to 12,180
sq km. Recent surveys indicate that the
longterm decline in NEC continues. For
example, surveys for the species in early
2008 documented the presence of NEC
in 7 of the 23 New Hampshire locations
that were known to be occupied in 2002
and 2003. Similarly, surveys in Maine
found the species present in 12 of 57
sites identified in an extensive survey
that spanned the years 2000 to 2004.
Unlike the New Hampshire study,
several new sites were documented in
Maine during 2008. Some have
suggested that the decline in NEC
occurrences in 2008 may be attributed
to persistent snow cover throughout
northern New England during the
winter of 2007–2008. Similar surveys
were conducted during the winter of
2009 in Maine, New Hampshire, Rhode
Island, and New York. The results are
pending further analysis. It is estimated
that less than one-third of the occupied
sites occur on lands in conservation
status and fewer than 10 percent are
being managed for early-successional
forest species.
The primary threat to the New
England cottontail is loss of habitat
through succession and alteration.
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69237
Isolation of occupied patches by areas of
unsuitable habitat and high predation
rates are resulting in local extirpation of
New England cottontails from small
patches. The range of the New England
cottontail has contracted by 75 percent
or more since 1960 and current land
uses in the region indicate that the rate
of change, about 2 percent range loss per
year, will continue. Additional threats
include competition for food and habitat
with introduced eastern cottontails and
large numbers of native white-tailed
deer; inadequate regulatory mechanisms
to protect habitat; and mortality from
predation. The magnitude of the threats
continues to be high, because they occur
rangewide, and have a severe negative
effect on the survival of the species.
They are imminent because they are
ongoing. Thus, we retained an LPN of 2
for this species. Conservation measures
that address the threats to the species
are being developed.
Fisher, West Coast DPS (Martes
pennanti)—The following summary is
based on information contained in our
files and in the Service’s initial
warranted-but-precluded finding
published in the Federal Register on
April 8, 2004 (68 FR 18770). The fisher
is a carnivore in the family Mustelidae
and is the largest member of the genus
Martes. Historically, the West Coast
population of the fisher extended south
from British Columbia into western
Washington and Oregon, and in the
North Coast Ranges, Klamath-Siskiyou
Mountains, and Sierra Nevada in
California. Because of a lack of
detections with standardized survey
efforts over much of the fisher’s
historical range, the fisher is believed to
be extirpated or reduced to scattered
individuals from the lower mainland of
British Columbia through Washington
and northern Oregon and in the central
and northern Sierra Nevada in
California. Native extant populations of
fisher are isolated to the North Coast of
California, the Klamath-Siskiyou
Mountains of northern California and
southern Oregon, and the southern
Sierra Nevada in California.
Descendents of a fisher reintroduction
effort also occur in the southern
Cascades in Oregon. The Washington
Department of Fish and Wildlife in
conjunction with the Olympic National
Park has completed the third year of a
reintroduction effort as the State’s first
step in implementing their recover goals
for fisher. The California Department of
Fish and Game and other collaborators
began the first year of their translocation
efforts into the northern Sierra Nevada
during the winter of 2009–2010.
Estimates of fisher numbers in native
populations of the West Coast DPS vary
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widely. A rigorous monitoring program
is lacking for the northern California
southern Oregon and southern Oregon
Cascades populations, making estimates
of fisher numbers for these two
populations difficult. The fisher
monitoring program in the southern
Sierra Nevada population has provided
preliminary estimates indicating no
decline in the index of abundance
within the monitored portion of the
population. There is a high degree of
genetic relatedness within some
populations. The two populations of
native fisher in the northern California
southern Oregon and southern Sierra
Nevada are separated by four times the
species’ maximum dispersal distance.
The extant fisher populations are either
small (southern Sierra Nevada and
southern Oregon Cascades) and are
isolated from one another or both.
Major threats that fragment or remove
key elements of fisher habitat include
various forest vegetation management
practices such as timber harvest and
fuels-reduction treatments. Other
potential major threats in portions of the
range include: Large stand-replacing
wildfires, changes in forest composition
and structure related to climate change
effects, forest and fuels management,
and urban and rural development.
Threats to fishers that lead to direct
mortality and injury include: Collisions
with vehicles; predation; and viral
borne diseases such as rabies,
parvovirus, and canine distemper.
Existing regulatory mechanisms on
Federal, State, and private lands do not
provide sufficient protection for the key
elements of fisher habitat, or the
certainty that conservation efforts will
be effective or implemented. The
magnitude of threats is high as they
occur across the range of the DPS
resulting in a negative impact on fisher
distribution and abundance. However,
the threats are nonimminent as the
greatest long-term risks to the fisher in
its west coast range are the subsequent
ramifications of the isolation of small
populations and their interactions with
the listed threats. The three remaining
areas containing fisher populations
appear to be stable or not rapidly
declining based on recent survey and
monitoring efforts. Therefore, we
assigned an LPN of 6 to this DPS.
New Mexico meadow jumping mouse
(Zapus hudsonius luteus)—The
following summary is based on
information contained in our files and
the petition we received October 15,
2008. The New Mexico meadow
jumping mouse (jumping mouse) is
endemic to New Mexico, Arizona, and
a small area of southern Colorado. The
jumping mouse nests in dry soils but
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uses moist, streamside, dense riparian/
wetland vegetation. Recent genetic
studies confirm that the New Mexico
meadow jumping mouse is a distinct
subspecies from other Zapus hudsonius
subspecies, confirming the currently
accepted subspecies designation.
The threats that have been identified
are excessive grazing pressure, water
use and management, highway
reconstruction, development, recreation,
and beaver removal.
Since the early to mid-1990s over 100
historical localities have been surveyed.
Currently only 24 are extant, 11 in New
Mexico (including one that is
contiguous with the Colorado locality)
and 13 in Arizona. Moreover, the highly
fragmented nature of its distribution is
also a major contributor to the
vulnerability of this species and
increases the likelihood of very small,
isolated populations being extirpated.
The insufficient number of secure
populations, and the destruction,
modification, or curtailment of its
habitat, continue to pose the most
immediate threats to this species.
Because the threats affect the jumping
mouse in all but two of the extant
localities, the threats are of a high
magnitude. These threats are currently
occurring and, therefore, are imminent.
Thus, we continue to assign an LPN of
3 to this subspecies.
Mazama pocket gopher (Thomomys
mazama ssp. couchi, douglasii,
glacialis, louiei, melanops, pugetensis,
tacomensis, tumuli, yelmensis)—The
following summary is based on
information contained in our files. No
new information was provided in the
petition received December 11, 2002.
Seven of the nine subspecies of pocket
gopher are associated with glacial
outwash prairies in western Washington
(T. m. melanops is found on alpine
meadows in Olympic National Park, and
T. m. oregonus is found in extreme
southwest Washington). Of these seven
subspecies, five are likely still extant
(couchi, glacialis, pugetensis, tumuli,
and yelmensis). Few of these glacial
outwash prairies remain in Washington
today. Historically, such prairies were
patchily distributed, but the area they
occupied totaled approximately 170,000
acres (Stinson 2005). Now, residential
and commercial development and ingrowth of woody and/or nonnative
vegetation have further reduced their
numbers. In addition, development in or
adjacent to these prairies has likely
increased predation on Mazama pocket
gophers by dogs and cats.
The magnitude of threat is high due
to populations with patchy and isolated
distributions in habitats highly desirable
for development and subject to a wide
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variety of human activities that
permanently alter the habitat. The threat
of invasive plant species to the quality
of a highly specific habitat requirement
is high and constant. There are few
known populations of each subspecies.
A limited dispersal capability, and the
loss and degradation of additional
patches of appropriate habitat will
further isolate populations and increase
their vulnerability to extinction. Loss of
any of the subspecies will reduce the
genetic diversity and the likelihood of
continued existence of the T. mazama
subspecies complex in Washington.
The threats are imminent. Two of the
subspecies (Cathlamet and Tacoma) are
likely extinct. The status of T. m.
douglasii is unknown, but its location in
a matrix of towns means it’s threatened
by encroaching development. Two
gravel pits are operating on part of the
remaining Roy Prairie pocket gopher
habitat, and another one occurs in the
area of the Tenino pocket gopher. The
largest populations of two other
subspecies (Shelton and Olympia) are
located on airports with planned
development. Yelm pocket gophers are
also threatened by proposed
development. Due to its low genetic
diversity, isolation, and potential for
natural habitat alterations in the future,
T. m. melanops (Olympic pocket
gopher) is susceptible to stochastic
events and small population effects
such as genetic drift and founder effects.
Thus, we assign an LPN of 3 to these
subspecies.
Gunnison’s prairie dog (Cynomys
gunnisoni)—This species occurs in
Arizona, Colorado, New Mexico, and
Utah. However, only the significant
portion of the range in the montane
portions of central and south central
Colorado and north central New Mexico
is included on our list of candidates.
Within this portion of the range, plague
has significantly reduced the number
and size of populations, resulting in
considerable effects to the species.
Populations within montane habitat
have distinct disadvantages in resisting
the effects of plague due to a high
abundance of fleas that spread plague,
small populations that cannot recover in
numbers from plague epizootics, and
isolated populations that limit the
ability to recolonize. Poisoning and
shooting continue to be threats to the
Gunnison’s prairie dog within the
montane portion of its range and
contribute to the decline of the species
when combined with the effects of
disease. Agriculture, urbanization,
roads, and oil and gas development each
currently affect a small percentage of
Gunnison’s prairie dog habitat. Plague is
significantly affecting the remaining
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small, isolated populations. Plague
epizootics can extirpate populations
there within a short timeframe (3 to 10
years). We have assigned an LPN of 3 to
this species due to imminent threats of
a high magnitude in a significant
portion of its range.
Southern Idaho ground squirrel
(Spermophilus brunneus endemicus)—
The following summary is based on
information contained in our files. No
new information was provided in the
petition we received on May 11, 2004.
The southern Idaho ground squirrel is
endemic to four counties in southwest
Idaho; its total known range is
approximately 425,630 hectares
(1,051,752 acres). Threats to southern
Idaho ground squirrels include: Habitat
degradation and fragmentation; direct
killing from shooting, trapping, or
poisoning; predation; competition with
Columbian ground squirrels; and
inadequacy of existing regulatory
mechanisms. Habitat degradation and
fragmentation appear to be the primary
threats to the species. Nonnative
annuals now dominate much of this
species’ range, have changed the species
composition of vegetation used as forage
for the southern Idaho ground squirrel,
and have altered the fire regime by
accelerating the frequency of wildfire.
Habitat deterioration, destruction, and
fragmentation contribute to the current
patchy distribution of southern Idaho
ground squirrels. Based on recent
genetic work, southern Idaho ground
squirrels are subject to more genetic
drift and inbreeding than expected.
Two Candidate Conservation
Agreements with Assurances (CCAAs)
have been completed for this species in
recent years. Both CCAAs include
conservation measures that provide
additional protection to southern Idaho
ground squirrels from recreational
shooting and other direct killing on
enrolled lands, and also allow the State
of Idaho, the Service, and BLM to
investigate ways of restoring currently
degraded habitat. At this time, the
acreage enrolled through these two
CCAAs is 38,756 ha (95,767 ac), or
9 percent of the known range
approximately. While the ongoing
conservation efforts have helped to
reduce the magnitude of threats to
moderate, habitat degradation remains
the primary threat to the species
throughout most of its range. This threat
is imminent due to the ongoing and
increasing prevalence and dominance of
nonnative vegetation, and the current
patchy distribution of the species. Thus,
we assign an LPN of 9 to this
subspecies.
Washington ground squirrel
(Spermophilus washingtoni)—The
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following summary is based on
information contained in our files and
in the petition we received on March 2,
2000. The Washington ground squirrel
is endemic to the Deschutes–Columbia
Plateau sagebrush-steppe and grassland
communities in eastern Oregon and
south-central Washington. Although
widely abundant historically, recent
surveys suggest that its current range
has contracted toward the center of its
historical range. Approximately twothirds of the Washington ground
squirrel’s total historical range has been
converted to agricultural and residential
uses. The most contiguous, leastdisturbed expanse of suitable habitat
within the species’ range occurs on a
site owned by Boeing, Inc. and on the
Naval Weapons Systems Training
Facility near Boardman, Oregon. In
Washington, the largest expanse of
known suitable habitat occurs on State
and Federal lands.
Agricultural, residential, and
windpower development, among other
forms of development, continue to
eliminate Washington ground squirrel
habitat in portions of its range.
Throughout much of its range,
Washington ground squirrels are
threatened by the establishment and
spread of invasive plant species,
particularly cheatgrass, which alter
available cover and food quantity and
quality, and increase fire intervals.
Additional threats include habitat
fragmentation, recreational shooting,
genetic isolation and drift, and
predation. Potential threats include
disease, drought, and possible
competition with related species in
disturbed habitat at the periphery of
their range. In Oregon, some threats are
being addressed as a result of the State
listing of this species, and by
implementation of the Threemile
Canyon Farms Multi-Species Candidate
Conservation Agreement with
Assurances (CCAA). In Washington,
there are currently no formal agreements
with private landowners or with State or
Federal agencies to protect the
Washington ground squirrel.
Additionally, no State or Federal
management plans have been developed
that specifically address the needs of the
species or its habitat. Since current and
potential threats are widespread and, in
some cases, severe, we conclude the
magnitude of threats remains high. The
Washington ground squirrel has both
imminent and nonimminent threats. At
a range-wide scale, we conclude the
threats are nonimminent based largely
on the following: The CCAA addressed
the imminent loss of a large portion of
habitat to agriculture, there are no other
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large-scale efforts to convert suitable
habitat to agriculture, and windpower
project impacts can be minimized
through compliance with the Oregon
State Endangered Species Act (OESA)
and/or the Columbia Basin Ecoregion
wind energy siting and permitting
guidelines. We also consider the
potential development of shooting
ranges on the Naval Weapons Systems
Training Facility as nonimminent
because the proposed action is still
being developed, making us unable to
assess its timing and impact, which
could be minimized through
compliance with the OESA. We,
therefore, have retained an LPN of 5 for
this species.
Birds
Spotless crake, American Samoa DPS
(Porzana tabuensis)—The following
summary is based on information
contained in our files. No new
information was provided in the
petition we received on May 11, 2004.
Porzana tabuensis is a small, dark,
cryptic rail found in wetlands and rank
scrub or forest in the Philippines,
Australia, Fiji, Tonga, Society Islands,
Marquesas, Independent Samoa, and
American Samoa (Ofu, Tau). The genus
Porzana is widespread in the Pacific,
where it is represented by numerous
island-endemic and flightless species
(many of which are extinct as a result
of anthropogenic disturbances) as well
as several more cosmopolitan species,
including P. tabuensis. No subspecies of
P. tabuensis are recognized.
The American Samoa population is
the only population of spotless crakes
under U.S. jurisdiction. The available
information indicates that distinct
populations of the spotless crake, a
species not noted for long-distance
dispersal, are definable. The population
of spotless crakes in American Samoa is
discrete in relation to the remainder of
the species as a whole, which is
distributed in widely separated
locations. Although the spotless crake
(and other rails) have dispersed widely
in the Pacific, island rails have tended
to reduce or lose their power of flight
over evolutionary time and so become
isolated (and vulnerable to terrestrial
predators such as rats). The population
of this species in American Samoa is
therefore distinct based on geographic
and distributional isolation from
spotless crake populations on other
islands in the oceanic Pacific, the
Philippines, and Australia. The
American Samoa population of the
spotless crake links the Central and
Eastern Pacific portions of the species’
range. The loss of this population would
result in an increase of roughly 500
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miles (805 kilometers) in the distance
between the central and eastern
Polynesian portions of the spotless
crake’s range, and could result in the
isolation of the Marquesas and Society
Islands populations by further limiting
the potential for even rare genetic
exchange. Based on the discreteness and
significance of the American Samoa
population of the spotless crake, we
consider this population to be a distinct
vertebrate population segment.
Threats to this population have not
changed over the past year. The
population in American Samoa is
threatened by small population size,
limited distribution, predation by
nonnative mammals, continued
development of wetland habitat, and
natural catastrophes such as hurricanes.
The co-occurrence of a known predator
of ground-nesting birds, the Norway rat
(Rattus norvegicus), along with the
extremely restricted observed
distribution and low numbers, indicate
that the magnitude of the threats to the
American Samoa DPS of the spotless
crake continues to be high, because the
threats significantly affect the species
survival. The threats are ongoing, and
therefore imminent. Based on this
assessment of existing information
about the imminence and high
magnitude of these threats, we assigned
the spotless crake an LPN of 3.
Yellow-billed cuckoo, western U.S.
DPS (Coccyzus americanus)—The
following summary is based on
information contained in our files and
the petition we received on February 9,
1998. See also our 12-month petition
finding published on July 25, 2001 (66
FR 38611). The yellow-billed cuckoo is
a medium-sized bird of about 12 inches
(30 centimeters) in length with a
slender, long-tailed profile and a fairly
stout and slightly down-curved bill.
Plumage is grayish-brown above and
white below, with rufous primary flight
feathers with the tail feathers boldly
patterned with black and white below.
Western cuckoos breed in large blocks
of riparian habitats (particularly
woodlands with cottonwoods (Populus
fremontii) and willows (Salix sp.).
Dense understory foliage appears to be
an important factor in nest-site
selection, while cottonwood trees are an
important foraging habitat in areas
where the species has been studied in
California. We consider the yellowbilled cuckoos that occur in the western
United States as a distinct population
segment (DPS). The area for this DPS is
west of the crest of the Rocky
Mountains.
The threats currently facing the
yellow-billed cuckoo include habitat
loss, over-grazing, and pesticide
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application. Principal causes of riparian
habitat losses are conversion to
agricultural and other uses, dams and
river-flow management, stream
channelization and stabilization, and
livestock grazing. Available breeding
habitats for cuckoos have also been
substantially reduced in area and
quality by groundwater pumping and
the replacement of native riparian
habitats by invasive nonnative plants,
particularly tamarisk. Overuse by
livestock has been a major factor in the
degradation and modification of
riparian habitats in the western United
States. The effects include changes in
plant community structure and species
composition and in relative abundance
of species and plant density. These
changes are often linked to more
widespread changes in watershed
hydrology. Livestock grazing in riparian
habitats typically results in reduction of
plant species diversity and density,
especially of palatable broadleaf plants
like willows and cottonwood saplings,
and is one of the most common causes
of riparian degradation. In addition to
destruction and degradation of riparian
habitats, pesticides may affect cuckoo
populations. In areas where riparian
habitat borders agricultural lands— e.g.,
in California’s Central Valley—
pesticide use may indirectly affect
cuckoos by reducing prey numbers, or
by poisoning nestlings if sprayed
directly in areas where the birds are
nesting. A group comprised of Federal,
State, and nongovernmental agencies
organized by the Service (Region 8,
Sacramento Fish and Wildlife Office) is
in the process of completing a
rangewide conservation assessment and
strategy for the Western yellow-billed
cuckoo. The assessment is in early
stages of development, with work
beginning on a conservation strategy
expected in 2011. The LPN for the
yellow-billed cuckoo remains a 3, with
imminent threats of high magnitude.
Friendly ground-dove, American
Samoa DPS (Gallicolumba stairi)—The
following summary is based on
information contained in our files. No
new information was provided in the
petition we received on May 11, 2004.
The genus Gallicolumba is distributed
throughout the Pacific and Southeast
Asia. The genus is represented in the
oceanic Pacific by six species: Three are
endemic to Micronesian islands or
archipelagos, two are endemic to island
groups in French Polynesia, and G.
stairi is endemic to Samoa, Tonga, and
Fiji. Some authors recognize two
subspecies of the friendly ground-dove,
one, slightly smaller, in the Samoan
archipelago (G. s. stairi), and one in
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Tonga and Fiji (G. s. vitiensis), but
because morphological differences
between the two are minimal, we are
not recognizing separate subspecies at
this time.
In American Samoa, the friendly
ground-dove has been found on the
islands of Ofu and Olosega (Manua
Group). Threats to this subspecies have
not changed over the past year.
Predation by nonnative species and
natural catastrophes such as hurricanes
are the primary threats to the
subspecies. Of these, predation by
nonnative species is thought to be
occurring now and likely has been
occurring for several decades. This
predation may be an important
impediment to increasing the
population. Predation by introduced
species has played a significant role in
reducing, limiting, and extirpating
populations of island birds, especially
ground-nesters like the friendly grounddove, in the Pacific and other locations
worldwide. Nonnative predators known
or thought to occur in the range of the
friendly ground-dove in American
Samoa are feral cats (Felis catus),
Polynesian rats (Rattus exulans), black
rats (R. rattus), and Norway rats (R.
norvegicus).
In January 2004 and February of 2005,
hurricanes virtually destroyed the
habitat of G. stairi in the area on Olosega
Island that the species had been most
frequently recorded. Although this
species has coexisted with severe storms
for millennia, this example illustrates
the potential for natural disturbance to
exacerbate the effect of anthropogenic
disturbance on small populations.
Consistent monitoring using a variety of
methods over the last 5 years yielded
few observations and no change in the
relative abundance of this taxon in
American Samoa. The total population
size is poorly known, but is unlikely to
number more than a few hundred pairs.
The distribution of the friendly grounddove is limited to steep, forested slopes
with an open understory and a substrate
of fine scree or exposed earth; this
habitat is not common in American
Samoa. The threats are ongoing and,
therefore, imminent and the magnitude
is moderate because the relative
abundance has remained the same for
several years. Thus, we assign this
subspecies an LPN of 9.
Streaked horned lark (Eremophila
alpestris strigata)—The following
summary is based on information
contained in our files. No new
information was provided in the
petition we received on December 11,
2002. The streaked horned lark occurs
in Washington and Oregon, and is
thought to be extirpated in British
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Columbia, Canada. The streaked horned
lark nests on bare ground in sparsely
vegetated sites in short-grass dominated
habitats, such as native prairies, coastal
dunes, fallow and active agricultural
fields, seasonal wetlands, moderately- to
heavily-grazed pastures, seasonal
mudflats, airports, and dredgedeposition sites in and along the tidal
reach of the Columbia River. In
Washington, surveys show that there are
approximately 330 remaining breeding
birds. In Oregon, the breeding
population is estimated to be over 500
birds.
The streaked horned lark’s breeding
habitat continues to be threatened by
loss and degradation due to conversion
of native grasslands to other uses (such
as agriculture, homes, recreational areas,
and industry), encroachment of woody
vegetation, invasion of nonnative plant
species (e.g., Scot’s broom, sod-forming
grasses, and beachgrasses), and
dredging-related activities. Native
prairies have been nearly eliminated
throughout the range of the species. It is
estimated that less than 1 to 3 percent
of the native grassland and savanna
remains. And those that remain have
been invaded by nonnative sod-forming
grasses. Coastal nesting areas have
suffered the same fate. A recent
purchase of prairie lands in Washington
has secured habitat that would have
been developed. Its status as suitable
lark nesting habitat is unknown.
Wintering habitats are seemingly few,
and are susceptible to unpredictable
conversion to unsuitable over-wintering
habitat, plant succession, and invasion
by nonnative plants. Where larks
inhabit manmade habitats similar in
structure to native prairies (such as
airports, military reservations,
agricultural fields, and dredge-formed
islands), or where they occur adjacent to
human habitation, they are subjected to
a variety of unintentional human
disturbances. These include mowing,
recreational and military activities,
plowing, flooding, and dredge-material
deposition during the nesting season, as
well as intentional disturbances such as
at the Joint Base Lewis–McChord Field
where falcons and a dog are used to
haze birds in order to avoid aircraft
collisions, and the biennial (but
opposite year) RODEO and Air Expo
events that occur on or adjacent to lark
nesting habitat. In some areas,
landowners have taken steps to improve
streaked horned lark nesting habitat.
The magnitude of threat is high due
to small populations with low genetic
diversity, rapidly declining populations,
and patchy and isolated habitats in
areas desirable for development, many
of which remain unsecured. The threat
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of invasive plant species is high and
constant, aside from a few restoration
sites. The numbers of individuals are
low and the numbers of populations are
few. In addition, estimates of lambda
using data from all Washington sites
suggest a rapidly declining population.
Over-wintering birds are concentrated
in larger flocks and subject to
unpredictable wintering habitat loss
(especially in Oregon), potentially
affecting a large portion of the
population at one time. In Washington,
known populations occur on airports,
military bases, coastal beaches, and
Columbia River islands, where
management, training activities,
recreation, and dredge-material
deposition continue to negatively
impact streaked horned lark breeding
and wintering (although current work
being conducted by TNC may ultimately
lessen this last threat). In Oregon,
breeding and wintering sites occur on
Columbia River islands, in cultivated
grass fields, grazed pastures, fallow
fields, roadside shoulders, Christmas
tree farms, seasonal wetlands, restored
wet prairie, and wetland mudflats. Such
areas continue to be subject to negative
impacts such as dredge material
deposition, development, plowing,
mowing, pesticide and herbicide
applications, trampling, vehicle traffic,
and recreation.
The threats are imminent, as a result
of continued loss of suitable lark
habitat, high nest-predation rates, low
adult survival, and low fecundity. Low
adult survival and fecundity rates in the
Puget lowlands are of particular
concern. Loss of habitat is being caused
by development on and adjacent to
several of its nesting areas, including
continued expansions of the Fort Lewis
Gray Army Airfield West Ramp and the
Olympia Airport. Wintering populations
are at risk in Oregon due to the manner
in which larks gather in large flocks that
are vulnerable to stochastic events, and
also due to the fact that their wintering
habitat occurs on privately owned
agricultural lands that are subject to
unpredictable conversion. Other
ongoing threats include those occurring
on the Joint Base Lewis-McChord Field
(hazing birds off the airfields, RODEO,
and Air Expo). Based on imminent
threats of a high magnitude, we
continue to assign an LPN of 3 to this
subspecies.
Red knot (Calidris canutus rufa)—The
following summary is based on
information contained in our files and
information provided by petitioners.
Four petitions to emergency list the red
knot have been received: One on August
9, 2004, two others on August 5, 2005,
and the most recent on February 27,
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2008. The rufa subspecies is one of six
recognized subspecies of red knot, and
one of three subspecies occurring in
North America. This subspecies makes
one of the longest-distance migrations
known in the animal kingdom, as it
travels between breeding areas in the
central Canadian Arctic and wintering
areas that are primarily in southern
South America along the coast of Chile
and Argentina. They migrate along the
Atlantic coast of the United States,
where they may be found from Maine to
Florida.
The Delaware Bay area (in Delaware
and New Jersey) is the largest known
spring migration stopover area, with far
fewer migrants congregating elsewhere
along the Atlantic coast. The
concentration in the Delaware Bay area
occurs from the middle of May to early
June, corresponding to the spawning
season of horseshoe crabs. The knots
feed on horseshoe crab eggs, rebuilding
energy reserves needed to complete
migrations to the Arctic and arrive on
the breeding grounds in good condition.
In the past, horseshoe crab eggs at
Delaware Bay were so numerous that a
knot could dependably eat enough in
two to three weeks to double its weight.
Surveys at wintering areas and at
Delaware Bay during spring migration
indicate a substantial decline in the red
knot in recent years. At the Delaware
Bay area, peak counts between 1982 and
1998 were as high as 95,360 individuals.
Counts may vary considerably between
years. Some of the fluctuations can be
attributed to predator-prey cycles in the
breeding grounds, and counts show that
knots rebound from such reductions.
Peak counts of red knots observed
during aerial surveys flown in Delaware
Bay from 2004 to 2008 were consistently
below 16,000 birds, with an alltime low
of only 12,375 red knots found in 2007.
In recent years, the highest
concentrations of red knots at the
Delaware Bay stopover have been
within Mispillion Harbor, Delaware, an
area that has likely been undercounted
during past aerial surveys. Beginning in
2009, a new survey methodology was
implemented for the Delaware Bay
stopover area to include ground counts
that more accurately reflect
concentrations of red knots using
Mispillion Harbor and to include aerial
surveys of red knots using Atlantic
coastal marshes near Stone Harbor, New
Jersey. The highest count using the new
methodology showed 27,187 red knots
in Delaware and 900 in New Jersey, for
a total count of 28,087 birds. Poor
weather conditions in 2009 prevented
aerial surveys during the period when
red knots were thought to be at a peak,
so no comparison with the past aerial
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survey peak count method was possible.
While the number of red knots using
Delaware Bay likely increased in 2009,
much of the increase is attributed to
improved survey methods and an
expanded area of coverage.
Counts in recent years in South
America also are substantially lower
than in the past. In the mid-1980s, an
estimated 67,500 red knots were
observed from Tierra del Fuego, Chile
and along the coast of Argentina to
northern Patagonia. Since 2003, the
largest concentrations of red knots have
occurred at the principal wintering
areas in Bahia Lomas and other portions
of Tierra del Fuego and southern
Patagonia, with few birds found further
north along the coast of Argentina. More
than 50,000 red knots were counted in
the principal winter areas in 1985 and
2000. Since 2005, fewer than 18,000
have been counted within the same
area, with only 16,260 red knots
observed in 2010.
The primary threat to the red knot has
been attributed to destruction and
modification of its habitat, particularly
the reduction in key food resources
resulting from reductions in horseshoe
crabs, which are harvested primarily for
use as bait and secondarily to support
a biomedical industry. Commercial
harvest increased substantially in the
1990s. Research shows that since 1998,
a high proportion of red knots leaving
the Delaware Bay failed to achieve
threshold departure masses needed to
fly to breeding grounds and survive an
initial few days of snow cover, and this
corresponded to reduced annual
survival rates and reduced reproductive
success. Since 1999, to protect the
Atlantic coast population of the
horseshoe crab and to increase
availability of horseshoe crab eggs in
Delaware Bay for hemispheric migratory
shorebird populations, a series of timing
restrictions and substantially lower
harvest quotas have been adopted by the
Atlantic States Marine Fisheries
Commission, as well as by the States of
New Jersey, Delaware, and Maryland. In
March 2008, New Jersey passed
legislation imposing a moratorium on
horseshoe crab harvest or landing
within the State until such time as the
red knot has fully recovered.
The reductions in commercial
horseshoe crab harvest by Atlantic
coastal States since 1999 are substantial.
From 2004 to 2009, annual landings of
horseshoe crabs have been reduced by
over 70 percent from the reference
period landings of the mid- to late1990s. For Delaware and New Jersey,
the decline in horseshoe crab landings
for bait has decreased from 726,660
reported in 1999 to a preliminary
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number of 102,659 crabs landed in
Delaware in 2009 and no crabs
harvested in New Jersey. No horseshoe
crabs have been landed for bait in New
Jersey since 2007 as a result of the Stateimposed harvest moratorium. In the
Delaware Bay area, continued
recruitment of small horseshoe crabs
has been observed, with a substantial
increase in numbers of the smallest
sizes of immature males and females in
2009 over previous years. The
continued increase in immature males
and females would be expected in a
recovering population and suggests
recent harvest restrictions may be
having the desired effect, but it may be
several more years until this increase is
realized in spawning age adults, as
horseshoe crabs need 8 to10 years to
reach sexual maturity.
Other identified threat factors include
habitat destruction due to beach erosion
and various shoreline protection and
stabilization projects that are affecting
areas used by migrating knots for
foraging, the inadequacy of existing
regulatory mechanisms, human
disturbance, and competition with other
species for limited food resources. Also,
the concentration of red knots in the
Delaware Bay areas and at a relatively
small number of wintering areas makes
the species vulnerable to potential largescale events such as oil spills or severe
weather. Overall, we conclude that the
threats, in particular the modification of
habitat through harvesting of horseshoe
crabs, are severe enough to put the
viability of the knot at substantial risk
and is therefore of a high magnitude.
The threats are currently occurring, and
therefore imminent because of
continuing suppressed horseshoe-crabegg forage conditions for red knot
within the Delaware Bay stopover.
Based on imminent threats of a high
magnitude, we retain an LPN of 3 for
this subspecies.
Yellow-billed loon (Gavia adamsii)—
The following summary is based on
information contained in our files and
the petition we received on April 5,
2004. The yellow-billed loon is a
migratory bird. Solitary pairs breed on
lakes in the arctic tundra of the United
States, Russia, and Canada from June to
September. During the remainder of the
year, the species winters in more
southern coastal waters of the Pacific
Ocean and the Norway and North Seas.
During most of the year, individual
yellow-billed loons are so widely
dispersed that high adult mortality from
any single factor is unlikely. However,
during migration, yellow-billed loons
are more concentrated and are subject to
subsistence harvest that at current levels
appears to be unsustainable, based on
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the best available information; the
population could decline substantially
if such harvest continues. Future
subsistence harvests in Alaska, by
themselves, constitute a threat to the
species rangewide. This subsistence
harvest is occurring despite the species
being closed to hunting under the
Migratory Bird Treaty Act. In addition,
up to several hundred yellow-billed
loons may be taken annually on Russian
breeding grounds, and small numbers of
yellow-billed loons are reported in
harvests in other areas in Alaska outside
of the subsistence harvest area and in
Canada.
Other risk factors evaluated, including
oil and gas development (i.e.,
disturbance, changes in freshwater
chemistry and pollutant loads, and
changes in freshwater hydrology);
pollution; overfishing; climate change;
vessel traffic; commercial- and
subsistence-fishery bycatch; and
contaminants other than those
associated with oil and gas, were not
found to be threats to the species.
Although these other risk factors may
not rise to the level of a threat
individually, when taken collectively
with the effects of subsistence hunting
in other areas, they may reduce the
rangewide population even further. One
or more of the threats discussed above
is occurring throughout the range of the
yellow-billed loon, either in its breeding
or wintering grounds, or during
migration; therefore, the threats are
imminent. The magnitude of the
primary threat to the species,
subsistence harvest, is moderate.
Although subsistence harvest is
ongoing, the numbers taken have varied
substantially between years. In addition,
we have concerns about the precision of
the numbers reported. Thus, we
assigned the yellow-billed loon an LPN
of 8.
Kittlitz’s murrelet (Brachyramphus
brevirostris)—The following summary is
based on information contained in our
files and the petition we received on
May 9, 2001. Kittlitz’s murrelet is a
small diving seabird whose entire North
American population, and a majority of
the world’s population, inhabits
Alaskan coastal waters discontinuously
from Point Lay south to northern
portions of Southeast Alaska. Most
Kittlitz’s murrelets are associated with
tidewater glaciers, but some occur in
areas not currently influenced by
glaciers. Genetic analyses suggest very
low rates of immigration and emigration
between Kittlitz’s murrelets in the
western Aleutian Islands, where there
are no extant glaciers, and birds
occupying mainland fjords, where there
are glaciers today. For 2010, we estimate
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the world-wide abundance of Kittlitz’s
murrelets to be between 30,900 and
56,800 individuals. In some regions of
Alaska, Kittlitz’s murrelets have
declined at a rate of up to 20 percent
between two decadal periods (1988–
1999 and 2004–2007).
Threats to Kittlitz’s murrelets include
large-scale processes such as global
climate change and marine regime
shifts. These large-scale processes may
influence Kittlitz’s murrelet survival
and reproduction. Glacial retreat is a
global phenomenon that affects many of
the glaciers with which Kittlitz’s
murrelets are associated. This glacial
retreat may be changing forage fish
availability, and may contribute to loss
of nesting habitat and increased
predation on Kittlitz’s murrelets. Other
threats include oil spills, bycatch in
commercial gillnet fisheries, and
disturbance by tour boats. Catastrophic
events such as oil spills could have a
significant negative effect on the
population of this already diminished
species. Kittlitz’s murrelets are believed
to have been negatively affected by the
Exxon Valdez oil spill in Prince William
Sound in 1989. Mortality as bycatch in
commercial fishing may be a significant
factor in their population decline. Tour
boat visitation to glacial fjords is a
growing industry, and this activity may
increasingly disrupt Kittlitz’s murrelet
feeding behavior; tour boats may also
provide artificial perch sites for avian
predators.
Based on the observed population
trajectory and the severity of ongoing
threats (rapid glacial retreat, acute and
chronic oil spills, commercial gillnet
fishing, and human disturbance from
tour boats), the threats to this species
are high in magnitude and imminent.
Therefore, we assigned an LPN of 2 to
this species.
Xantus’s murrelet (Synthliboramphus
hypoleucus)—The following summary is
based on information contained in our
files and the petition we received on
April 16, 2002. The Xantus’s murrelet is
a small seabird in the family Alcidae
that occurs along the west coast of North
America in the United States, Mexico,
and Canada. The species has a limited
breeding distribution, only nesting on
the Channel Islands in southern
California and on islands off the west
coast of Baja California, Mexico.
Although data on population trends are
scarce, the population is suspected to
have declined greatly over the last
century, mainly due to introduced
predators such as rats (Rattus sp.) and
feral cats (Felis catus) to nesting islands,
with possible extirpations on three
islands in Mexico. A dramatic decline
(up to 70 percent) from 1977 to 1991
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was detected at the largest nesting
colony in southern California, possibly
due to high levels of predation on eggs
by the endemic deer mouse (Peromyscus
maniculatus elusus). Identified threats
include introduced predators at nesting
colonies, oil spills and oil pollution,
reduced prey availability, human
disturbance, and artificial light
pollution.
Although substantial declines in the
Xantus’s murrelet population likely
occurred over the last century, some of
the largest threats are being addressed,
and, to some degree, ameliorated.
Declines and possible extirpations at
several nesting colonies were thought to
have been caused by nonnative
predators, which have been removed
from many of the islands where they
once occurred. Most notably, since
1994, Island Conservation and Ecology
Group has systematically removed rats,
cats, and dogs from every murrelet
nesting colony in Mexico, with the
exception of cats and dogs on
Guadalupe Island. In 2002, rats were
eradicated from Anacapa Island in
southern California, which has resulted
in improvements in reproductive
success at that island. In southern
California, efforts to restore nesting
habitat on Santa Barbara Island through
the Montrose Settlements Restoration
Project may benefit the Xantus’s
murrelet population at that island.
Artificial lighting from squid fishing
and other vessels, or lights on islands,
remains a potential threat to the species.
Bright lights make Xantus’s murrelets
more susceptible to predation, and they
can also become disoriented and
exhausted from continual attraction to
bright lights. Chicks can become
disoriented and separated from their
parents at sea, which could result in
death of the dependent chicks. Highwattage lights on commercial market
squid (Loligo opalescens) fishing vessels
used at night to attract squid to the
surface of the water in the Channel
Islands was the suspected cause of
unusually high predation on Xantus’s
murrelets by western gulls (Larus
occidentalis) and barn owls (Tyto alba)
at Santa Barbara Island in 1999. To
address this threat, in 2000, the
California Fish and Game Commission
required light shields and a limit of
30,000 watts per boat; it is unknown if
this is sufficient to reduce impacts.
Since 1999, no significant squid fishing
has occurred near any of the colonies in
the Channel Islands; however, this
remains a potential future threat.
A proposal to build three liquid
natural gas facilities near the Channel
Islands could affect the nesting colonies
due to bright lights at night from the
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facility and visiting tanker vessels, noise
from the facilities or from helicopters
visiting the facilities, and the threat of
oil spills associated with visiting tanker
vessels. However, these facilities are
early in the complex and long-term
planning processes, and it is possible
that none of these facilities will be built.
In addition, none of them are directly
adjacent to nesting colonies, where their
impacts would be expected to be more
significant. The remaining threats to the
species are of a high magnitude but
nonimminent. Therefore, we retained an
LPN of 5 for this species.
Lesser prairie-chicken (Tympanuchus
pallidicinctus)—The following
summary is based on information
contained in our files and the petition
received on October 5, 1995. Additional
information can be found in the
12-month finding published on June 7,
1998 (63 FR 31400). Biologists estimate
that the occupied range has declined by
92 percent since the 1800s. The most
serious threats to the lesser prairiechicken are loss of habitat from
conversion of native rangelands to
introduced forages and cultivated crops;
conversion of suitable restored habitat
in the Conservation Reserve Program to
cropland; cumulative habitat
degradation caused by severe grazing;
and energy development, including
transmission, and wind, oil, and gas
development. Additional threats are
woody plant invasion of open prairies
due to fire suppression, herbicide use
(including resumption of herbicide use
in shinnery oak habitat), and habitat
fragmentation caused by structural and
transportation developments. Many of
these threats may exacerbate the normal
effects of periodic drought on lesser
prairie-chicken populations. In many
cases, the remaining suitable habitat has
become fragmented by the spatial
arrangement of these individual threats.
Habitat fragmentation can be a threat to
the species through several
mechanisms: Remaining habitat patches
may become smaller than necessary to
meet the requirements of individuals
and populations, necessary habitat
heterogeneity may be lost to areas of
homogeneous habitat structure, and the
probability of recolonization decreases
as the distance between suitable habitat
patches expands. We have determined
that the overall magnitude of threats to
the lesser prairie-chicken throughout its
range is high, and that the threats are
ongoing, and thus imminent.
Consequently, we have retained an LPN
of 2 for this species.
Greater sage-grouse (Centrocercus
urophasianus), Columbia Basin DPS—
The following summary is based on
information in our files and a petition,
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dated May 14, 1999, requesting the
listing of the Washington population of
the western sage-grouse (C. u. phaios).
On May 7, 2001, we concluded that
listing the Columbia Basin DPS of the
western sage-grouse was warranted, but
precluded by higher-priority listing
actions (66 FR 22984); this population
was historically found in northern
Oregon and central Washington.
Following our May 7, 2001, finding, the
Service received additional petitions
requesting listing actions for various
other greater sage-grouse populations,
including one for the nominal western
subspecies, dated January 24, 2002, and
three for the entire species, dated June
18, 2002, and March 19 and December
22, 2003. The Service subsequently
found that the petition for the western
subspecies did not present substantial
information (68 FR 6500), and that
listing the greater sage-grouse
throughout its historical range was not
warranted (70 FR 2244). These latter
findings were remanded to the Service
for further consideration. In response,
we initiated a new range-wide status
review for the entire species (73 FR
10218). On March 5, 2010, we found
that listing of the greater sage-grouse
was warranted but precluded by higher
priority listing actions (75 FR 13909;
March 23, 2010), and it was added to
the list of candidates. We also found
that the western subspecies of the
greater sage-grouse, the taxonomic
entity we relied on in our DPS analysis
for the Columbia Basin population, was
no longer considered a valid subspecies.
In light of our conclusions regarding the
invalidity of the western sage-grouse
subspecies, the significance of the
Columbia Basin DPS to the greater sagegrouse will require further review. As
priorities allow the Service intends to
complete an analysis to determine if this
population continues to warrant
recognition as a DPS in accordance with
our Policy Regarding the Recognition of
Distinct Population (61 FR 4722;
February 7, 1996). Until that time, the
Columbia Basin DPS will remain a
candidate for listing as a separate
population of greater sage-grouse. Even
if this population does not meet our
DPS policy, the greater sage-grouse
population in the Columbia Basin will
remain a candidate for listing as part of
the greater sage-grouse entity.
Band-rumped storm-petrel, Hawaii
DPS (Oceanodroma castro)—The
following summary is based on
information contained in our files and
the petition we received on May 8,
1989. No new information was provided
in the second petition received on May
11, 2004. The band-rumped storm-petrel
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is a small seabird that is found in
several areas of the subtropical Pacific
and Atlantic Oceans. In the Pacific,
there are three widely separated
breeding populations—one in Japan,
one in Hawaii, and one in the
Galapagos. Populations in Japan and the
Galapagos are comparatively large and
number in the thousands, while the
Hawaiian birds represent a small,
remnant population of possibly only a
few hundred pairs. Band-rumped stormpetrels are most commonly found in
close proximity to breeding islands. The
three populations in the Pacific are
separated by long distances across the
ocean where birds are not found.
Extensive at-sea surveys of the Pacific
have revealed a broad gap in
distribution of the band-rumped stormpetrel to the east and west of the
Hawaiian Islands, indicating that the
distribution of birds in the central
Pacific around Hawaii is disjunct from
other nesting areas. The available
information indicates that distinct
populations of band-rumped stormpetrels are definable and that the
Hawaiian population is distinct based
on geographic and distributional
isolation from other band-rumped
storm-petrel populations in Japan, the
Galapagos, and the Atlantic Ocean. A
population also can be considered
discrete if it is delimited by
international boundaries that have
differences in management control of
the species. The Hawaiian population of
the band-rumped storm-petrel is the
only population within U.S. borders or
under U.S. jurisdiction. Loss of the
Hawaiian population would cause a
significant gap in the distribution of the
band-rumped storm-petrel in the
Pacific, and could result in the complete
isolation of the Galapagos and Japan
populations without even occasional
genetic exchanges. Therefore, the
population is both discrete and
significant, and constitutes a DPS.
The band-rumped storm-petrel
probably was common on all of the
main Hawaiian Islands when
Polynesians arrived about 1,500 years
ago, based on storm-petrel bones found
in middens on the island of Hawaii and
in excavation sites on Oahu and
Molokai. Nesting colonies of this
species in the Hawaiian Islands
currently are restricted to remote cliffs
on Kauai and Lehua Island and highelevation lava fields on Hawaii.
Vocalizations of the species were heard
in Haleakala Crater on Maui as recently
as 2006; however, no nesting sites have
been located on the island to date. The
significant reduction in numbers and
range of the band-rumped storm-petrel
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is due primarily to predation by
nonnative predators introduced by
humans, including the domestic cat
(Felis catus), small Indian mongoose
(Herpestes auropunctatus), common
barn owl (Tyto alba), black rat (R.
rattus), Polynesian rat (R. exulans), and
Norway rat (R. norvegicus), which occur
throughout the main Hawaiian Islands,
with the exception of the mongoose,
which is not established on Kauai.
Attraction of fledglings to artificial
lights, which disrupts their night-time
navigation, resulting in collisions with
building and other objects, and
collisions with artificial structures such
as communication towers and utility
lines are also threats. Erosion of nest
sites caused by the actions of nonnative
ungulates is a potential threat in some
locations. Efforts are under way in some
areas to reduce light pollution and
mitigate the threat of collisions, but
there are no large-scale efforts to control
nonnative predators in the Hawaiian
Islands. The threats are imminent
because they are ongoing, and they are
of a high magnitude because they can
severely affect the survival of this DPS
leading to a relatively high likelihood of
extinction. Therefore, we assign this
distinct population segment an LPN of
3.
Elfin-woods warbler (Dendroica
angelae)—The following summary is
based on information contained in our
files. No new information was provided
in the petition we received on May 11,
2004. Dendroica angelae, or elfin-woods
warbler, is a small entirely black and
white warbler, distinguished by its
white eyebrow stripe, white patches on
ear covers and neck, incomplete eye
ring, and black crown. The elfin-woods
warbler was at first thought to occur
only in the high elevation dwarf or elfin
forests, but has since been found at
lower elevations including shade coffee
plantations and secondary forests. This
species builds a compact cup nest,
usually close to the trunk and well
hidden among the epiphytes of a small
tree, and its breeding season extends
from March to June. It forages in the
middle part of trees, gleaning insects
from leaves in the outer portion of the
tree crown. The elfin-woods warbler has
been documented from four locations in
Puerto Rico: Luquillo Mountains (El
Yunque National Forest), Sierra de
Cayey, and the Commonwealth forests
of Maricao and Toro Negro. However, it
has not been recorded again in Toro
Negro and Cayey, following the passing
of Hurricane Hugo in 1989. In 2003 and
2004, surveys were conducted for the
elfin-woods warbler in the Carite
Commonwealth Forest, Toro Negro
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Forest, Guilarte Forest, Bosque del
Pueblo, Maricao Forest and the El
Yunque National Forest, but only
detected the species in the latter two. In
the Maricao Commonwealth Forest, 778
elfin woods warblers were recorded,
and in the El Yunque National Forest,
196 elfin-woods warblers were
recorded.
The elfin-woods warbler is currently
threatened by habitat modification.
Destruction of elfin forest and
Podocarpus forest by the installation of
infrastructure (e.g., telecommunication
towers, recreational facilities) threatens
the long-term survival of this species.
Loss of this type of habitat has been
curtailed but potential for loss still
exists due to Commonwealth agencies
other than DNER. Furthermore,
restoration of this habitat would take
decades to complete. Present regulatory
processes, both Commonwealth and
Federal, promote the protection of these
areas. Conversion of elfin-woods
warbler habitat of better quality (e.g.,
mature secondary forests, young
secondary forests, and shaded-coffee
plantations) along the periphery of the
Maricao Commonwealth Forest to
marginal habitat (e.g., pastures, dry
slope forests, residential rural forests,
gallery forests, and un-shaded coffee
plantations) may result in ineffective
corridors for dispersal and expansion of
elfin-woods warbler populations. While
there is an effort to restore sun-coffee
plantations to shade-coffee habitat,
other habitats adjacent to the Maricao
Forest may still be affected by
residential development.
The listing priority number was
originally assessed as a 5 (high
magnitude, non-imminent threats). This
was changed during the 2009 CNOR.
Our analysis of the five listing factors
revealed that only factors A and D
applied to the species. Although habitat
modification is occurring, it is limited,
as the species is found mostly on
protected lands managed by the
Commonwealth and Federal agencies.
We found no indication that the two
populations of elfin-woods warbler are
declining in numbers. We also found
that it can thrive in disturbed and
plantation habitats, and rebounds and
recovers well, in a relatively short time,
from the damaging effects of hurricanes
to the forest structure. Therefore, the
magnitude of threats is moderate to low.
These threats are not imminent, because
most of the range of the elfin-woods
warbler is within protected lands. As a
result, we assigned an LPN of 11 to this
species.
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Reptiles
Northern Mexican Gartersnake
(Thamnophis eques megalops)—The
following summary is based on
information contained in our files. The
northern Mexican gartersnake generally
occurs in three types of habitat:
(1) Ponds and cienegas; (2) lowland
river riparian forests and woodlands;
and (3) upland stream gallery forests.
Within the United States, the
distribution of the northern Mexican
gartersnake has been reduced by close to
90 percent and it occurs in fragmented
populations within the middle/upper
Verde River drainage, middle/lower
Tonto Creek, and the upper Santa Cruz
River, as well as in a small number of
isolated wetland habitats in
southeastern Arizona; its status in New
Mexico is uncertain. Within Mexico, the
northern Mexican gartersnake is
distributed along the Sierra Madre
Occidental and the Mexican Plateau in
the Mexican states of Sonora,
Chihuahua, Durango, Coahila,
Zacatecas, Guanajuato, Nayarit, Hidalgo,
´
Jalisco, San Luis Potosı, Aguascalientes,
´
´
Tlaxacala, Puebla, Mexico, Michoacan,
´
Oaxaca, Veracruz, and Queretaro. The
primary threat to the northern Mexican
gartersnake is competition and
predation from nonnative species such
as sportfish, bullfrogs, and crayfish.
Degradation and elimination of its
habitat and native prey base are also
significant threats, most notably in areas
where nonnative species co-occur.
Threats, particularly competition and
predation by nonnative species, are high
in magnitude since they result in direct
mortality or reduced reproductive
capacity and may be irreversible in
complex habitat resulting in a relatively
high likelihood of extinction. The
threats are ongoing and, therefore,
imminent. Thus, we retained an LPN of
3 for this subspecies.
Sand dune lizard (Sceloporus
arenicolus)—We continue to find that
listing this species is warranted but
precluded as of the date of publication
of this notice. However, we are working
on a proposed listing rule that we
expect to publish prior to making the
next annual resubmitted 12-month
petition finding.
Eastern massasauga rattlesnake
(Sistrurus catenatus catenatus)—The
following summary is based on
information contained in our files. No
new information was provided in the
petition received on May 11, 2004. The
eastern massasauga is one of three
recognized subspecies of massasauga. It
is a small, thick-bodied rattlesnake that
occupies shallow wetlands and adjacent
upland habitat in portions of Illinois,
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Indiana, Iowa, Michigan, Minnesota,
Missouri, New York, Ohio,
Pennsylvania, Wisconsin, and Ontario.
Although the current range of S. c.
catenatus resembles the subspecies’
historical range, the geographic
distribution has been restricted by the
loss of the subspecies from much of the
area within the boundaries of that range.
Approximately 40 percent of the
counties that were historically occupied
by S. c. catenatus no longer support the
subspecies. S. c. catenatus is currently
listed as endangered in every State and
province in which it occurs, except for
Michigan where it is designated as a
species of special concern. Each State
and Canadian province across the range
of S. c. catenatus has lost more than 30
percent, and for the majority more than
50 percent, of their historical
populations. Furthermore, less than 35
percent of the remaining populations
are considered secure. Approximately
59 percent of the remaining S. c.
catenatus populations occur wholly or
in part on public land, and Statewide
and/or site-specific Candidate
Conservation Agreements with
Assurances (CCAAs) are currently being
developed for many of these areas in
Iowa, Illinois, Michigan, and Wisconsin.
In 2004, a Candidate Conservation
Agreement (CCA) with the Lake County
Forest Preserve District in Illinois was
completed. In 2005, a CCA with the
Forest Preserve District of Cook County
in Illinois was completed. In 2006, a
CCAA with the Ohio Department of
Natural Resources Division of Natural
Areas and Preserves was completed for
Rome State Nature Preserve in
Ashtabula County. The magnitude of
threats is moderate at this time.
However, populations soon to be under
CCAs and CCAAs have a low to
moderate likelihood of persisting and
remaining viable. Other populations are
likely to suffer additional losses in
abundance and genetic diversity and
some will likely be extirpated unless
threats are removed in the near future.
Declines have continued or may be
accelerating in several states. Thus, we
are monitoring the status of this species
to determine if a change in listing
priority is warranted. Furthermore, we
are working with several experts and
partners in the development of an
extinction risk model for the subspecies,
and the results of this work may
indicate that a change in listing priority
number is appropriate. Threats of
habitat modification, habitat succession,
incompatible land management
practices, illegal collection for the pet
trade, and human persecution are
ongoing and imminent threats to many
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remaining populations, particularly
those inhabiting private lands. We
conclude that emergency listing is not
warranted and have kept the LPN at 9
for this subspecies.
Black pine snake (Pituophis
melanoleucus lodingi)—The following
summary is based on information
contained in our files. No new
information was provided in the
petition we received on May 11, 2004.
There are historical records for the black
pine snake from one parish in
Louisiana, 14 counties in Mississippi,
and 3 counties in Alabama west of the
Mobile River Delta. Black pine snake
surveys and trapping indicate that this
species has been extirpated from
Louisiana and from four counties in
Mississippi. Moreover, the distribution
of remaining populations has become
highly restricted due to the destruction
and fragmentation of the remaining
longleaf pine habitat within the range of
the subspecies. Most of the known
Mississippi populations are
concentrated on the DeSoto National
Forest. Populations occurring on
properties managed by State and other
governmental agencies as gopher
tortoise mitigation banks or wildlife
sanctuaries represent the best
opportunities for long-term survival of
the subspecies in Alabama. Other
factors affecting the black pine snake
include vehicular mortality and low
reproductive rates, which magnify the
threats from destruction and
fragmentation of longleaf pine habitat
and increase the likelihood of local
extinctions. Due to the imminent threats
of high magnitude caused by the past
destruction of most of the longleaf pine
habitat of the black pine snake, and the
continuing persistent degradation of
what remains, we assigned an LPN of 3
to this subspecies.
Louisiana pine snake (Pituophis
ruthveni)—The following summary is
based on information contained in our
files and the petition we received on
July 19, 2000. The Louisiana pine snake
historically occurred in the firemaintained longleaf pine ecosystem
within west-central Louisiana and
extreme east-central Texas. Most of the
historical longleaf pine habitat of the
Louisiana pine snake has been
destroyed or degraded due to logging,
fire suppression, roadways, shortrotation silviculture, and grazing. In the
absence of recurrent fire, suitable
habitat conditions for the Louisiana
pine snake and its primary prey, the
Baird’s pocket gopher (Geomys
breviceps), are lost due to vegetative
succession. The loss and fragmentation
of the longleaf pine ecosystem has
resulted in extant Louisiana pine snake
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populations that are isolated and small.
Trapping and occurrence data indicate
the Louisiana pine snake is currently
restricted to seven disjunct populations;
five of the populations occur on federal
lands and two occur mainly on private
industrial timberlands. Currently
occupied habitat in Louisiana and Texas
is estimated to be approximately
163,000 acres, with 53 percent occurring
on public lands and 47 percent in
private ownership.
All remnant Louisiana pine snake
populations have been affected by
habitat loss and all require active habitat
management. A Candidate Conservation
Agreement (CCA) was completed in
2003 to maintain and enhance occupied
and potential habitat on public lands,
and to protect known Louisiana pine
snake populations. On Federal lands,
signatories of the Louisiana pine snake
CCA currently conduct habitat
management (i.e., prescribed burning
and thinning) that is beneficial to the
Louisiana pine snake. This proactive
habitat management has likely slowed
or reversed the rate of Louisiana pine
snake habitat degradation on many
portions of federal lands. The largest
extant Louisiana pine snake population
exists on private industrial timberlands.
Although two conservation areas are
managed to benefit Louisiana pine
snakes on this property, the majority of
the intervening occupied habitat is
threatened by land management
activities (habitat conversion to shortrotation pine plantations) that decrease
habitat quality.
Three of the remnant Louisiana pine
snake populations may be vulnerable to
decreased demographic viability or
other factors associated with low
population sizes and demographic
isolation. Although these remnant
Louisiana pine snake populations are
intrinsically vulnerable and thus
threatened by these factors, it is not
known if they are presently actually
facing these threats. Because all extant
populations are currently isolated and
fragmented by habitat loss in the matrix
between populations, there is little
potential for dispersal among remnant
populations or for the natural recolonization of vacant habitat patches.
Thus, the loss of any remnant
population is likely to be permanent.
Other factors affecting the Louisiana
pine snake throughout its range include
low fecundity, which magnifies other
threats and increases the likelihood of
local extirpations, and vehicular
mortality, which may significantly affect
Louisiana pine snake populations.
While the extent of Louisiana pine
snake habitat loss has been great in the
past and much of the remaining habitat
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has been degraded, habitat loss does not
represent an imminent threat, primarily
because the rate of habitat loss appears
to be declining on public lands.
However, all populations require active
habitat management, and the lack of
adequate habitat remains a threat for
several populations. The potential
threats to a large percentage of extant
Louisiana pine snake populations,
coupled with the likely permanence of
these effects and the species’ low
fecundity and low population sizes
(based on capture rates and occurrence
data), lead us to conclude that the
threats have significant effect on the
survival of the species and therefore
remain high in magnitude. Thus, based
on nonimminent, high-magnitude
threats, we assign a listing priority
number of 5 to this species.
Sonoyta mud turtle (Kinosternon
sonoriense longifemorale)—The
following summary is based on
information contained in our files. No
new information was provided in the
petition we received on May 11, 2004.
The Sonoyta mud turtle occurs in a
spring and pond at Quitobaquito
Springs on Organ Pipe Cactus National
Monument in Arizona, and in the Rio
Sonoyta and Quitovac Spring of Sonora,
Mexico. Loss and degradation of stream
habitat from water diversion and
groundwater pumping, along with its
very limited distribution, is the primary
threat to the Sonoyta mud turtle.
Sonoyta mud turtles are highly aquatic
and depend on permanent water for
survival. The area of southwest Arizona
and northern Sonora where the Sonoyta
mud turtle occurs is one of the driest
regions of the southwest. Continuing
drought, irrigated agriculture, and
development in the region, is expected
to cause surface water in the Rio
Sonoyta to dwindle further and
therefore have a significant impact on
the survival of this subspecies, which
may also be vulnerable to aerial
spraying of pesticides on nearby
agricultural fields. We retained an LPN
of 3 for this subspecies because threats
are of a high magnitude and continue to
date, and therefore are imminent.
Amphibians
Columbia spotted frog, Great Basin
DPS (Rana luteiventris)—The following
summary is based on information
contained in our files and the petition
we received on May 1, 1989. Currently,
Columbia spotted frogs appear to be
widely distributed throughout
southwestern Idaho, southeastern
Oregon, northeastern and central
Nevada, but local populations within
this general area appear to be small and
isolated from each other. Recent work
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by researchers in Idaho and Nevada
have documented the loss of historically
known sites, reduced numbers of
individuals within local populations,
and declines in the reproduction of
those individuals. Small, highly
fragmented populations, characteristic
of the majority of existing populations
of Columbia spotted frogs in the Great
Basin, are highly susceptible to
extinction processes.
Poor management of Columbia
spotted frog habitat—including water
development, improper grazing, mining
activities, and nonnative species—has
and continues to contribute to the
degradation and fragmentation of
habitat. Emerging fungal diseases such
as chytridiomycosis and the spread of
parasites may be contributing factors to
Columbia spotted frog population
declines throughout portions of its
range. Effects of climate change, such as
drought, and stochastic events such as
fire often have detrimental effects to
small isolated populations and can often
exacerbate existing threats. A 10-year
Conservation Agreement and Strategy
was signed in September 2003 for both
the Northeast and the Toiyabe
subpopulations in Nevada. The goals of
the conservation agreements are to
reduce threats to Columbia spotted frogs
and their habitat to the extent necessary
to prevent populations from becoming
extirpated throughout all or a portion of
their historical range and to maintain,
enhance, and restore a sufficient
number of populations of Columbia
spotted frogs and their habitat to ensure
their continued existence throughout
their historical range. Additionally, a
Candidate Conservation Agreement with
Assurances was completed in 2006 for
the Owyhee subpopulation at Sam
Noble Springs, Idaho. Several habitat
enhancement projects have been
conducted throughout their range which
have benefitted these populations.
Based on imminent threats of moderate
magnitude, we assigned a listing
priority number of 9 to this DPS of the
Columbia spotted frog.
Mountain yellow-legged frog, Sierra
Nevada DPS (Rana muscosa)—The
following summary is based on
information contained in our files and
the petition received on February 8,
2000. Also see our 12-month petition
finding published on January 16, 2003
(68 FR 2283) and our amended
12-month petition finding published on
June 25, 2007 (72 FR 34657). The
mountain yellow-legged frog inhabits
the high-elevation lakes, ponds, and
streams in the Sierra Nevada Mountains
of California, from near 4,500 feet (ft)
(1,370 meters (m)) to 12,000 ft (3,650 m).
The distribution of the mountain
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yellow-legged frog is from Butte and
Plumas Counties in the north to Tulare
and Inyo Counties in the south. A
separate population in southern
California is already listed as
endangered (67 FR 44382). Based on
mitochondrial DNA, morphological, and
acoustic studies, Vredenburg et al.
recently recognized two distinct species
of mountain yellow-legged frog in the
Sierra Nevada, R. muscosa and R.
sierrae. This taxonomic distinction has
been recently adopted by the American
Society of Ichthyologists and
Herpetologists, the Herpetologists’
League, and the Society for the Study of
Amphibians and Reptiles. The
Vredenburg study determined that two
species exist, as described by Camp, but
have different geographical ranges than
first described. Camp described R.
muscosa as only occurring in southern
California. A recent study determined
that R. muscosa also occurs in the
southern portion of the Sierra Nevada,
and R. sierrae occurs both in the
southern and northern portions of the
Sierra Nevada, with no range overlap.
At this time, we have not adopted this
taxonomic distinction of two species
and continue to recognize mountain
yellow-legged frogs in the Sierra Nevada
Mountains of California as R. muscosa
and as the candidate entity.
Predation by introduced trout is the
best-documented cause of the decline of
the Sierra Nevada mountain yellowlegged frog, because it has been
repeatedly observed that fishes and
mountain yellow-legged frogs rarely coexist. Mountain yellow-legged frogs and
trout (native and nonnative) do co-occur
at some sites, but these co-occurrences
probably are mountain yellow-legged
frog populations with negative
population growth rates in the absence
of immigration. To help reverse the
decline of the mountain yellow-legged
frog, the Sequoia and Kings Canyon
National Parks have been removing
introduced trout since 2001. Over
18,000 introduced trout have been
removed from 11 lakes since the project
started in 2001. The lakes are
completely-to-mostly fish-free and
substantial mountain yellow-legged frog
population increases have resulted. The
California Department of Fish and Game
has also removed or is in the process of
removing nonnative trout from a total of
between 10 and 20 water bodies in the
Inyo, Humboldt-Toiyabe, Sierra, and El
Dorado National Forests. In the El
Dorado National Forest golden trout
were removed from Leland Lakes, and
attempts have been made to remove
trout from two sites near Gertrude Lake,
three lakes in the Pyramid Creek
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watershed, and a tributary of Cole
Creek; no data showing increase in
mountain yellow-legged frogs at these
sites is available.
In California, chytridiomycosis, more
commonly known as chytrid fungus
(Batrachochytrium dendrobatidis) or
Bd, has been detected in many
amphibian species, including the
mountain yellow-legged frog within the
Sierra Nevada. Recent research has
shown that this pathogenic fungus has
become widely distributed throughout
the Sierra Nevada, and that infected
mountain yellow-legged frogs often die
soon after metamorphosis. Several
infected and uninfected populations
were monitored in Sequoia and Kings
Canyon National Parks over multiple
years, documenting dramatic declines
and extirpations in infected but not in
uninfected populations. In the summer
of 2005, 39 of 43 populations assayed in
Yosemite National Park were positive
for chytrid fungus.
The current distribution of the Sierra
Nevada mountain yellow-legged frog is
restricted primarily to public lands at
high elevations, including streams,
lakes, ponds, and meadow wetlands
located on national forests, including
wilderness and non-wilderness on the
forests, and national parks. In several
areas where detailed studies of the
effects of chytrid fungus on the
mountain yellow-legged frog are ongoing, substantial declines have been
observed over the past several years. For
example, in 2007 surveys in Yosemite
National Park, mountain yellow-legged
frogs were not detectable at 37 percent
of 285 sites where they had been
observed in 2000–2002; in 2005 in
Sequoia and Kings Canyon National
Parks, mountain yellow-legged frogs
were not detected at 54 percent of sites
where they had been recorded 3 to 8
years earlier. A compounding effect of
disease-caused extinctions of mountain
yellow-legged frogs is that
recolonization may never occur, because
streams connecting extirpated sites to
extant populations now contain
introduced fishes, which act as barriers
to frog movement within
metapopulations. The most recent
assessment of the species status in the
Sierra Nevada indicates that mountainyellow legged frogs occur at less than 8
percent of the sites from which they
were historically observed. A group of
prominent scientists further suggest a 10
percent decline per year in the number
of remaining Rana mucosa populations
is likely. Based on threats that are
imminent (because they are ongoing)
and high-magnitude (because they
significantly affect the survival of the
DPS throughout its range), we continue
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to assign the population of mountain
yellow-legged frog in the Sierra Nevada
an LPN of 3.
Oregon spotted frog (Rana pretiosa)—
The following summary is based on
information contained in our files and
the petition we received on May 4,
1989. Historically, the Oregon spotted
frog ranged from British Columbia to the
Pit River drainage in northeastern
California. Based on surveys of
historical sites, the Oregon spotted frog
is now absent from at least 76 percent
of its former range. The majority of the
remaining Oregon spotted frog
populations are small and isolated.
The threats to the species’ habitat
include development, livestock grazing,
introduction of nonnative plant species,
vegetation succession, changes in
hydrology due to construction of dams
and alterations to seasonal flooding,
lack of management of exotic vegetation,
predators, and poor water quality.
Additional threats to the species are
predation by nonnative fish and
introduced bullfrogs; competition with
bullfrogs and nonnative fish for habitat;
and diseases, such as oomycete water
mold Saprolegnia and chytrid fungus
infections. The magnitude of threat is
high for this species because this wide
range of threats to both individuals and
their habitats could seriously reduce or
eliminate any of these isolated
populations and further reduce the
species’ range and potential survival.
Habitat restoration and management
actions have not prevented population
declines. The threats are imminent
because each population is faced with
multiple ongoing and potential threats
as identified above. Therefore, we retain
an LPN of 2 for the Oregon spotted frog.
Relict leopard frog (Lithobates
onca)—The following summary is based
on information contained in our files
and the petition we received on May 9,
2002. Natural relict leopard frog
populations are currently only known to
occur in two general areas in Nevada:
Near the Overton Arm area of Lake
Mead and Black Canyon below Lake
Mead. These two areas comprise a small
fraction of the historical distribution of
the species, which included: springs,
streams, and wetlands found within the
Virgin River drainage downstream from
the vicinity of Hurricane, Utah; along
the Muddy River, Nevada; and along the
Colorado River from its confluence with
the Virgin River downstream to Black
Canyon below Lake Mead, Nevada and
Arizona.
Suggested factors contributing to the
decline of the species include alteration
of aquatic habitat due to agriculture and
water development, including
regulation of the Colorado River, and
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the introduction of exotic predators and
competitors. In 2005, the National Park
Service, in cooperation with the Service
and various other Federal, State, and
local partners, developed a conservation
agreement and strategy intended to
improve the status of the species
through prescribed management actions
and protection. Conservation actions
identified for implementation in the
agreement and strategy include captive
rearing of tadpoles for translocation and
refugium populations, habitat and
natural history studies, habitat
enhancement, population and habitat
monitoring, and translocation. New sites
within the historical range of the species
have been successfully established with
captive-reared frogs. Conservation is
proceeding under the agreement and
strategy; however, additional time is
needed to determine whether or not the
agreement and strategy will be effective
in eliminating or reducing the threats to
the point that the relict leopard frog can
be removed from candidate status.
However, because of these conservation
efforts, the magnitude of existing threats
is low to moderate. These threats remain
nonimminent since there are no
pending projects or actions that would
adversely affect frog populations or
threaten surface water associated with
known sites occupied by the frog.
Therefore, we assigned an LPN of 11 to
this species.
Austin blind salamander (Eurycea
waterlooensis)—The following summary
is based on information contained in
our files. No new information was
provided in the petition received on
May 11, 2004. The Austin blind
salamander is known to occur in and
around three of the four spring sites that
comprise the Barton Springs complex in
the City of Austin, Travis County,
Texas. Primary threats to this species
are degradation of water quality due to
expanding urbanization. The Austin
blind salamander depends on a constant
supply of clean water in the Edwards
Aquifer discharging from Barton Springs
for its survival. Urbanization
dramatically alters the normal
hydrologic regime and water quality of
an area. Increased impervious cover
caused by development increases the
quantity and velocity of runoff that
leads to erosion and greater pollution
transport. Pollutants and contaminants
that enter the Edwards Aquifer are
discharged in salamander habitat at
Barton Springs and could have serious
morphological and physiological effects
to the salamander.
The Texas Commission on
Environmental Quality adopted the
Edwards Rules in 1995 and 1997, which
require a number of water quality
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protection measures for new
development occurring in the recharge
and contributing zones of the Edwards
Aquifer. However, Chapter 245 of the
Texas Local Government Code permits
‘‘grandfathering’’ of State regulations.
Grandfathering allows developments to
be exempted from any new local or
State requirements for water quality
controls and impervious cover limits if
the developments were planned prior to
the implementation of such regulations.
As a result of the grandfathering law,
very few developments have followed
the Edwards Rules. New developments
are still obligated to comply with
regulations that were applicable at the
time when project applications for
development were first filed. In
addition, it is significant that even if
they were followed with every new
development, the Edwards Rules do not
span the entire watershed for Barton
Springs. Consequently, development
occurring outside these jurisdictions can
have negative consequences on water
quality and thus have an impact on the
species.
Water-quality impacts threaten the
continued existence of the Austin blind
salamander by altering physical aquatic
habitats and the food sources of the
salamander. We consider the threats to
be imminent because urbanization is
ongoing and continues to expand over
the Barton Springs Segment of the
Edwards Aquifer and water quality
continues to degrade. While the City of
Austin and many other partners are
actively working on conservation of the
Barton Springs salamander, and the
Austin blind salamander benefits from
all of the ongoing conservation actions
that are being conducted for the Barton
Springs salamander, these efforts have
not yet been successful in improving
water quality. In addition, the existence
of the species continues to be threatened
by hazardous chemical spills within the
Barton Springs Segment of the Edwards
Aquifer, which could result in direct
mortality. Because the Austin blind
salamander is known from only three
clustered spring sites and must rely on
clear, clean spring discharges from the
Edwards Aquifer for its survival,
degraded water quality poses a severe
threat to the entire population, and is
therefore a high-magnitude threat. Thus,
we maintained the LPN of 2 for this
species.
Georgetown salamander (Eurycea
naufragia)—The following summary is
based on information contained in our
files. No new information was provided
in the petition received on May 11,
2004. The Georgetown salamander is
known from spring outlets along five
tributaries to the San Gabriel River and
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one cave in the City of Georgetown,
Williamson County, Texas. The
Georgetown salamander has a very
limited distribution and depends on a
constant supply of clean water from the
Northern Segment of the Edwards
Aquifer for its survival.
Primary threats to this species are
degradation of water quality due to
expanding urbanization. Increased
impervious cover by development
increases the quantity and velocity of
runoff that leads to erosion and greater
pollution transport. Pollutants and
contaminants that enter the Edwards
Aquifer are discharged from spring
outlets in salamander habitat and have
serious morphological and physiological
effects to individuals of the species.
The Texas Commission on
Environmental Quality adopted the
Edwards Rules in 1995 and 1997, which
require a number of water quality
protection measures for new
development occurring in the recharge
and contributing zones of the Edwards
Aquifer. New developments are still
obligated to comply with regulations
that were applicable at the time when
project applications were first filed.
However, Chapter 245 of the Texas
Local Government Code permits
‘‘grandfathering’’ of state regulations.
Grandfathering allows developments to
be exempted from any new local or state
requirements for water quality controls
and impervious cover limits if the
developments were planned prior to the
implementation of such regulations. As
a result of the grandfathering law, very
few developments have followed the
Edwards Rules. In addition, it is
significant that even if they were
followed with every new development,
the Edwards Rules do not span the
entire watershed for the Edwards
Aquifer. The TCEQ has developed
voluntary water-quality protection
measures for development in the
Edwards Aquifer region of Texas;
however, it is unknown if these
measures will be implemented
throughout a large portion of the
watershed or if they will be effective in
maintaining or improving water quality.
Development occurring outside the
TCEQ’s jurisdiction can have negative
consequences on water quality and thus
affect the species. Water-quality impacts
threaten the continued existence of the
Georgetown salamander by altering
physical aquatic habitats and the food
sources of the salamander. The threats
are imminent because urbanization is
ongoing and continues to expand over
the Northern Segment of the Edwards
Aquifer. However, Williamson County
and the Williamson County
Conservation Foundation are actively
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working to protect habitat and acquire
land within the contributing watershed
for the Georgetown salamander. Also,
they are conducting monitoring and
data collecting activities in an effort that
is expected to lead to the development
of a conservation strategy for this
species. These conservation actions
reduce the magnitude of the threat to
the Georgetown salamander to a
moderate level by reducing the amount
of development occurring in the portion
of the watershed that affects the species.
Thus, we maintained the LPN of 8 for
this species.
Jollyville Plateau salamander (Eurycea
tonkawae)—The following summary is
based on information gathered during a
status review of this species (72 FR
71039, December 13, 2007). The
Jollyville Plateau salamander occurs in
the Jollyville Plateau and Brushy Creek
areas of the Edwards Plateau in Travis
and WilliamsonCounties, Texas. This
species has a limited distribution and
depends on a constant supply of clean
water from the Northern Segment of the
Edwards Aquifer for its survival. The
primary threat to this species is
degradation of water quality due to
expanding urbanization. Increased
impervious cover by development
increases the quantity and velocity of
runoff that leads to erosion and greater
pollution transport. Pollutants and
contaminants that enter the Edwards
Aquifer are discharged from spring
outlets in salamander habitat and have
serious morphological and physiological
effects on individual of the species.
The Texas Commission on
Environmental Quality adopted the
Edwards Rules in 1995 and 1997, which
require a number of water quality
protection measures for new
development occurring in the recharge
and contributing zones of the Edwards
Aquifer. However, Chapter 245 of the
Texas Local Government Code permits
‘‘grandfathering’’ of state regulations.
Grandfathering allows developments to
be exempted from any new local or state
requirements for water quality controls
and impervious cover limits if the
developments were planned prior to the
implementation of such regulations. As
a result of the grandfathering law, very
few developments have followed the
Edwards Rules. New developments are
still obligated to comply with
regulations that were applicable at the
time when project applications for
development were first filed. In
addition, it is significant that even if
they were followed with every new
development, the Edwards Rules do not
span the entire watershed for the
Edwards Aquifer. The TCEQ has
developed voluntary water quality
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protection measures for development in
the Edwards Aquifer region of Texas;
however, it is unknown if these
measures will be implemented
throughout a large portion of the
watershed or if they will be effective in
maintaining or improving water quality.
Water-quality impacts threaten the
continued existence of the Jollyville
Plateau salamander by altering physical
aquatic habitats and the food sources of
the salamander, producing negative
population responses. Such responses
have been documented at both the
individual level (mortalities and
deformities) and the population level
(significant declines in abundance over
the last 10 years and extirpation at one
site). We find the overall negative
response by the salamander to be at a
moderate level because deformities and
deaths of salamanders have been limited
in scope to a few localities and only one
location may have experienced an
extirpation. Otherwise, the current
range of the salamander changed little
from the known historical range. Thus,
we maintained the LPN of 8 for this
species.
Salado salamander (Eurycea
chisholmensis)—The following
summary is based on information
contained in our files. No new
information was provided in the
petition we received on May 11, 2004.
The Salado salamander is historically
known from two spring sites, Big
Boiling Springs and Robertson Springs,
near Salado, Bell County, Texas. We
have received only one anecdotal report
of a salamander sighting in Big Boiling
Springs in 2008; prior to that, the
salamander had not been sighted there
since 1991. Texas Parks and Wildlife
Department has been conducting regular
surveys at Robertson Springs since June
2009 and has rediscovered the Salado
salamander at this site.
Primary threats to this species are
habitat modification and degradation of
water quality due to expanding
urbanization. The Salado salamander
depends on a constant supply of clean
water from the Northern Segment of the
Edwards Aquifer for its survival.
Pollutants and contaminants that enter
the Edwards Aquifer discharge in
salamander habitat and have
morphological and physiological effects
on the salamander. We do not know
how likely spills are to occur within the
contributing watersheds of the springs
that support this species. However,
several groundwater incidents have
occurred within Salado salamander
habitat in recent years. The salamander
is reasonably expected to be vulnerable
to catastrophic hazardous materials
spills, groundwater contamination from
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the Northern Segment of the Edwards
Aquifer, and impacts to its surface
habitat. In addition, Big Boiling Springs
is located near Interstate Highway 35
and in the center of the Village of
Salado. Traffic and urbanization is
likely to increase the threat of
contamination of spills, higher levels of
impervious cover, and subsequent
impacts to groundwater. These threats
significantly affect the survival of this
species, and groundwater contamination
and impacts to surface habitat are
ongoing. Moreover, we do not have
information that the magnitude or
imminence of the threats to the species
has changed since our previous
assessment when we concluded there
are ongoing, and therefore, imminent
threats of a high magnitude. Therefore,
we maintained the LPN of 2 for this
species.
Yosemite toad (Bufo canorus)—The
following summary is based on
information contained in our files and
the petition we received on April 3,
2000. See also our 12-month petition
finding published on December 10, 2002
(67 FR 75834). Yosemite toads are
moderately sized toads, with females
having black spots edged with white or
cream that are set against a grey, tan, or
brown background. Males have a nearly
uniform coloration of yellow-green to
olive drab to greenish brown. Yosemite
toads are most likely to be found in
areas with thick meadow vegetation or
patches of low willows near or in water,
and use rodent burrows for
overwintering and temporary refuge
during the summer. Breeding habitat
includes the edges of wet meadows,
slow-flowing streams, shallow ponds,
and shallow areas of lakes. The
historical range of Yosemite toads in the
Sierra Nevada occurs from the Blue
Lakes region north of Ebbetts Pass
(Alpine County) to south of Kaiser Pass
in the Evolution Lake/Darwin Canyon
area (Fresno County). The historical
elevational range of Yosemite toads is
1,460 to 3,630 m (4,790 to 11,910 ft).
The threats currently facing the
Yosemite toad include cattle grazing,
timber harvesting, recreation, disease,
and climate change. Inappropriate
grazing has been shown to cause loss in
vegetative cover and destroys peat
layers in meadows, which lowers the
groundwater table and summer flows.
This may increase the stranding and
mortality of tadpoles, or make these
areas completely unsuitable for
Yosemite toads. Grazing can also
degrade or destroy moist upland areas
used as non-breeding habitat by
Yosemite toads and collapse rodent
burrows used by Yosemite toads as
cover and hibernation sites. Timber
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harvesting and associated road
development can severely alter the
terrestrial environment and result in the
reduction and occasional extirpation of
amphibian populations in the Sierra
Nevada. They also create habitat gaps
that may act as dispersal barriers and
contribute to the fragmentation of
Yosemite toad habitat and populations.
Trails (foot, horse, bicycle, or offhighway motor vehicle) compact soil in
riparian habitat, which increases
erosion, displaces vegetation, and can
lower the water table. Trampling or the
collapsing of rodent burrows by
recreationists, pets, and vehicles could
lead to direct mortality of all life stages
of the Yosemite toad and disrupt their
behavior. Various diseases have been
confirmed in Yosemite toads. Mass dieoffs of amphibians have been attributed
to: chytrid fungal infections of
metamorphs and adults; Saprolegnia
fungal infections of eggs; iridovirus
infection of larvae, metamorphs, or
adults; and bacterial infections.
Yosemite toads probably are exposed to
a variety of pesticides and other
chemicals throughout their range.
Environmental contaminants could
negatively affect the species by causing
direct mortality; suppressing the
immune system; disrupting breeding
behavior, fertilization, growth or
development of young; and disrupting
the ability to avoid predation.
There is no indication that any of
these threats are ongoing or planned and
the threats are therefore nonimminent.
In addition, since there are a number of
substantial populations and these
threats tend to have localized effects,
the threats are moderate to low in
magnitude. In addition, almost all of the
species’ range occurs on Federal land,
which protects the species from private
development and facilitates
management of the species by Federal
agencies. We therefore retained an LPN
of 11 for the Yosemite toad.
Black Warrior waterdog (Necturus
alabamensis)—The following summary
is based on information contained in
our files. No new information was
provided in the petition we received on
May 11, 2004. The Black Warrior
waterdog is a salamander that inhabits
streams above the Fall Line within the
Black Warrior River Basin in Alabama.
There is very little specific locality
information available on the historical
distribution of the Black Warrior
waterdog since little attention was given
to this species between its description
in 1937 and the 1980s. At that time,
there were a total of only 11 known
historical records from 4 Alabama
counties. Two of these sites have now
been inundated by impoundments.
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Extensive survey work was conducted
in the 1990s to look for additional
populations. As a result of that work,
the species was documented at 14 sites
in 5 counties.
Water-quality degradation is the
biggest threat to the continued existence
of the Black Warrior waterdog. Most
streams that have been surveyed for the
waterdog showed evidence of pollution
and many appeared biologically
depauperate. Sources of point and
nonpoint pollution in the Black Warrior
River Basin have been numerous and
widespread. Pollution is generated from
inadequately treated effluent from
industrial plants, sanitary landfills,
sewage treatment plants, poultry
operations, and cattle feedlots. Surface
mining represents another threat to the
biological integrity of waterdog habitat.
Runoff from old, abandoned coal mines
generates pollution through
acidification, increased mineralization,
and sediment loading. The North River,
Locust Fork, and Mulberry Fork, all
streams that this species inhabits, are on
the Environmental Protection Agency’s
list of impaired waters. An additional
threat to the Black Warrior waterdog is
the creation of large impoundments that
have flooded thousands of square
hectares of its habitat. These
impoundments are likely marginal or
unsuitable habitat for the salamander.
Suitable habitat for the Black Warrior
waterdog is limited and available data
indicate extant populations are small
and their viability is questionable. This
situation is pervasive and problematic;
water quality issues are persistent and
regulatory mechanisms are not
ameliorating these threats, though we
have no indication of population
declines, at present. We hope additional
surveys may clarify the status of
populations in face of existing threats.
Therefore, the overall magnitude of the
threat is moderate. Water quality
degradation in the Black Warrior basin
is ongoing; therefore, the threats are
imminent. We assigned an LPN of 8 to
this species.
Fishes
Headwater chub (Gila nigra)—The
following summary is based on
information contained in our files, the
12-month finding published in the
Federal Register on May 3, 2006 (71 FR
26007), and in the petition received
November 9, 2009. The headwater chub
is a moderate-sized cyprinid fish. The
range of the headwater chub has been
reduced by approximately 60 percent.
Seventeen streams (125 miles (200
kilometers) of stream) are thought to be
occupied out of 27 streams (312 miles
(500 kilometers) of stream) formerly
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occupied in the Gila River Basin in
Arizona and New Mexico. All remaining
populations are fragmented and isolated
and threatened by a combination of
factors.
Headwater chub are threatened by
introduced nonnative fish that prey on
them and compete with them for food.
Habitat destruction and modification
have occurred and continue to occur as
a result of dewatering, impoundment,
channelization, and channel changes
caused by alteration of riparian
vegetation and watershed degradation
from mining, grazing, roads, water
pollution, urban and suburban
development, groundwater pumping,
and other human actions. Existing
regulatory mechanisms do not appear to
be adequate for addressing the impact of
nonnative fish and also have not
removed or eliminated the threats that
continue to be posed through habitat
destruction or modification. The
fragmented nature and rarity of existing
populations makes them vulnerable to
other natural or manmade factors, such
as drought and wildfire. Climate change
is predicted to worsen these threats
though increased aridity of the region,
thus reducing stream flows and
warming aquatic habitats, which makes
them more suitable to nonnative
species.
The Arizona Game and Fish
Department has finalized the Arizona
Statewide Conservation Agreement for
Roundtail Chub (G. robusta), Headwater
Chub, Flannelmouth Sucker
(Catostomus latipinnis), Little Colorado
River Sucker (Catostomus spp.),
Bluehead Sucker (C. discobolus), and
Zuni Bluehead Sucker (C. discobolus
yarrowi). The New Mexico Department
of Game and Fish recently listed the
headwater chub as endangered and
created a recovery plan for the species:
Colorado River Basin Chubs (Roundtail
Chub, Gila Chub (G. intermedia), and
Headwater Chub) Recovery Plan, which
was approved by the New Mexico State
Game Commission on November 16,
2006. Both the Arizona Agreement and
the New Mexico Recovery Plan
recommend preservation and
enhancement of extant populations and
restoration of historical headwater-chub
populations. The recovery and
conservation actions prescribed by
Arizona and New Mexico plans, which
we predict will reduce and remove
threats to this species, will require
further discussions and authorizations
before they can be implemented,
although some actions have been
completed and several are planned for
the immediate future. Although threats
are ongoing, existing information
indicates long-term persistence and
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stability of existing populations.
Currently 10 of the 17 extant stream
populations are considered stable based
on abundance and evidence of
recruitment. Based on our assessment,
threats (nonnative species, habitat loss
from land uses) remain imminent and
are of a moderate magnitude. Thus, we
have retained an LPN of 8 for this
species.
Roundtail Chub (Gila robusta) Lower
Colorado River Distinct Population
Segment—The following summary is
based on information contained in our
files and the 12-month finding
published in the Federal Register on
July 7, 2009 (74 FR 32352). The
roundtail chub is a moderate to large
cyprinid fish. The range of the roundtail
chub has been reduced by
approximately 68 to 82 percent. Thirtythree streams are currently occupied,
representing approximately 18 to 32
percent of the species’ former range, or
800 km (500 miles) to 1350 km (840 mi)
of 3050 km (1895 mi) of formerly
occupied streams in the Gila River Basin
in Arizona and New Mexico. Most of the
remaining populations are fragmented
and isolated, and all are threatened by
a combination of factors.
Roundtail chub are threatened by
introduced nonnative fish that prey on
them and compete with them for food.
Habitat destruction and modification
have occurred and continue to occur as
a result of dewatering, impoundment,
channelization, and channel changes
caused by alteration of riparian
vegetation and watershed degradation
from mining, grazing, roads, water
pollution, urban and suburban
development, groundwater pumping,
and other human actions. Existing
regulatory mechanisms do not appear to
be adequate for addressing the impact of
nonnative fish and also have not
removed or eliminated the threats that
continue to be posed through habitat
destruction or modification. The
fragmented nature and rarity of existing
populations makes them vulnerable to
other natural or manmade factors, such
as drought and wildfire. Climate change
is predicted to worsen these threats
though increased aridity of the region,
thus reducing stream flows and
warming aquatic habitats, which makes
them more suitable to nonnative
species.
The Arizona Game and Fish
Department has finalized the Arizona
Statewide Conservation Agreement for
Roundtail Chub, Headwater Chub (G.
nigra), Flannelmouth Sucker
(Catostomus latipinnis), Little Colorado
River Sucker (Catostomus spp.),
Bluehead Sucker (C. discobolus), and
Zuni Bluehead Sucker (C. discobolus
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yarrowi). The New Mexico Department
of Game and Fish lists the roundtail
chub as endangered and has created a
recovery plan for the species: Colorado
River Basin Chubs (Roundtail Chub,
Gila Chub (G. intermedia), and
Headwater Chub) Recovery Plan, which
was approved by the New Mexico State
Game Commission on November 16,
2006. Both the Arizona Agreement and
the New Mexico Recovery Plan
recommend preservation and
enhancement of extant populations and
restoration of historical roundtail-chub
populations. The recovery and
conservation actions prescribed by
Arizona and New Mexico plans, which
we predict will reduce and remove
threats to this species, will require
further discussions and authorizations
before they can be implemented,
although some actions have been
completed and several are planned for
the immediate future. Although threats
are ongoing, existing information
indicates long-term persistence and
stability of existing populations.
Currently 9 of the 33 extant stream
populations are considered stable based
on abundance and evidence of
recruitment. Based on our assessment,
threats (nonnative species, habitat loss
from land uses) remain imminent and
are of a moderate magnitude. Thus, we
have retained an LPN of 9 for this
distinct population segment.
Arkansas darter (Etheostoma
cragini)—The following summary is
based on information contained in our
files. No new information was provided
in the petition we received on May 11,
2004. This fish species occurs in
Arkansas, Colorado, Kansas, Missouri,
and Oklahoma. The species is found
most often in sand- or pebble-bottomed
pools of small, spring-fed streams and
marshes, with cool water and broadleaved aquatic vegetation. Its current
distribution is indicative of a species
that once was widely dispersed
throughout its range, but has been
relegated to isolated areas surrounded
by unsuitable habitat that prevents
dispersal. Factors influencing the
current distribution include: Surface
and groundwater irrigation resulting in
decreased flows or stream dewatering;
the dewatering of long reaches of
riverine habitat necessary for species
movement when surface flows do occur;
conversion of prairie to cropland which
influences groundwater recharge and
spring flows; water quality degradation
from a variety of sources; and the
construction of dams which act as
barriers preventing emigration upstream
and downstream through the reservoir
pool. The magnitude of threats facing
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this species is moderate to low, given
the number of different locations where
the species occurs and the fact that no
single threat or combination of threats
affects more than a portion of the
widespread population occurrences.
Overall, the threats are nonimminent
since groundwater pumping is declining
and development, spills, and runoff are
not currently affecting the species
rangewide. Thus, we are retaining an
LPN of 11 for the Arkansas darter.
Pearl darter (Percina aurora)—The
following summary is based on
information contained in our files. Little
is known about the specific habitat
requirements or natural history of the
Pearl darter, a small fish in the Percidae
family. Pearl darters have been collected
from a variety of river/stream attributes,
mainly over gravel bottom substrate.
This species is historically known only
from localized sites within the
Pascagoula and Pearl River drainages in
two states. Currently, the Pearl darter is
considered extirpated from the Pearl
River drainage and rare in the
Pascagoula River drainage. Since 1983,
the range of the Pearl darter has
decreased by 55 percent.
The Pearl darter is vulnerable to nonpoint-source pollution caused by
urbanization and other land use
activities; gravel mining and resultant
changes in river geomorphology,
especially head cutting; and the
possibility of water quantity decline
from the proposed Department of
Energy Strategic Petroleum Reserve
project and a proposed dam on the
Bouie River. Additional threats are
posed by the apparent lack of adequate
State and Federal water quality
regulations due to the continuing
degradation of water quality within the
species’ habitat. The Pearl darter’s
localized distribution and apparent low
population numbers may indicate a
species with lower genetic diversity
which would also make this species
more vulnerable to catastrophic events.
Threats affecting the Pearl darter are
localized in nature, affecting portions of
the population within the drainage,
thus, we assigned a threat magnitude of
moderate to low for this species. In
addition, the threats are imminent since
the identified threats are currently
impacting this species in some portions
of its range. Therefore, we have assigned
a listing priority number of 8 for this
species.
Grotto sculpin (Cottus sp., sp. nov.)—
The following summary is based on
information contained in our files. No
new information was provided in the
petition we received on May 11, 2004.
The Grotto sculpin, a small fish, is
restricted to two karst areas (limestone
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regions characterized by sink holes,
abrupt ridges, caves, and underground
streams), the Central Perryville Karst
and Mystery-Rimstone Karst in Perry
County, southeast Missouri. Grotto
sculpins have been documented in only
five cave systems (Burr et al. 2001, p.
284). The current overall range of the
grotto sculpin has been estimated to
encompass approximately 260 square
kilometers (100 square miles).
The small population size and
endemism of the grotto sculpin make it
vulnerable to extinction due to genetic
drift, inbreeding depression, and
random or chance changes to the
environment (Smith 1974, p. 350). The
species’ karst habitat is located downgradient of the city of Perryville,
Missouri, which poses a potential threat
if contaminants from this urban area
enter cave streams occupied by grotto
sculpins. Various agricultural
chemicals, such as ammonia, nitrite/
nitrate, acetochlor, dieldrin, and
atrazine have been detected at levels
high enough to be detrimental to aquatic
life within the Perryville Karst area.
Many of the sinkholes in Perry County
contain anthropogenic refuse, ranging
from household cleansers and sewage to
used pesticide and herbicide containers.
As a result, potential water
contamination from various sources of
point and non-point pollution poses a
significant threat to the grotto sculpin.
Of the five cave systems documented to
have grotto sculpins, populations in two
cave systems have had fish kills in
recent times. Predatory fish such as
common carp, fat-head minnow, yellow
bullhead, green sunfish, bluegill, and
channel catfish occur in all of the caves
occupied by grotto sculpin. These
potential predators may escape surface
farm ponds that unexpectedly drain
through sinkholes into the underground
cave systems and enter Grotto sculpin
habitat. No regulatory mechanisms are
in place that would provide protection
to the grotto sculpin. Current threats to
the habitat of the grotto sculpin may
exacerbate potential problems
associated with its low population
numbers and increase the likelihood of
extinction. Due to the high magnitude of
ongoing, and thus imminent, threats we
assigned this species an LPN of 2.
Sharpnose shiner (Notropis
oxyrhynchus)—The following summary
is based on information contained in
our files. No new information was
provided in the petition we received on
May 11, 2004. The sharpnose shiner is
a small, slender minnow, endemic to
the Brazos River Basin in Texas.
Historically, the sharpnose shiner
existed throughout the Brazos River and
several of its major tributaries. It has
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also been found in the Wichita River
(within the Red River Basin), where it
may have once naturally occurred but
has since been extirpated. Current
information indicates that the
population upstream of Possum
Kingdom Reservoir is apparently stable,
while the population downstream of the
reservoir may be extirpated,
representing a reduction of
approximately 69 percent of its
historical range.
The most significant threat to the
existence of the sharpnose shiner is
potential reservoir development within
its current range. The current water plan
for Texas provides several reservoir
options that could be implemented
within the Brazos River drainage.
Additional threats include irrigation
and water diversion, sedimentation,
desalination, industrial and municipal
discharges, agricultural activities, instream sand and gravel mining, and the
spread of invasive saltcedar. The current
limited distribution of the sharpnose
shiner within the Upper Brazos River
Basin makes it vulnerable to
catastrophic events such as the
introduction of competitive species or
prolonged drought. State law does not
provide protection for the sharpnose
shiner. The magnitude of threat is
considered high since reservoir
development within the species’ current
range may render remaining habitat
unsuitable. The threats are
nonimminent because the most
significant threat—major reservoir
projects—is not likely to occur in the
near future, and there is potential for
implementing other water-supply
options that could preclude reservoir
development. For these reasons, we
assigned an LPN of 5 to this species.
Smalleye shiner (Notropis buccula)—
The following summary is based on
information contained in our files. No
new information was provided in the
petition we received on May 11, 2004.
The smalleye shiner is a small, pallid
minnow endemic to the Brazos River
Basin in Texas. The population of
smalleye shiners within the Upper
Brazos River drainage (upstream of
Possum Kingdom Reservoir) is
apparently stable. However, the shiner
may be extirpated downstream from the
reservoir, representing a reduction of
approximately 54 percent of its
historical range.
The most significant threat to the
existence of the smalleye shiner is
potential reservoir development within
its current range. The current water plan
for Texas provides several reservoir
options that could be implemented
within the Brazos River drainage.
Additional threats include irrigation
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and water diversion, sedimentation,
desalination, industrial and municipal
discharges, agricultural activities, instream sand and gravel mining, and the
spread of invasive saltcedar. The current
limited distribution of the smalleye
shiner within the Upper Brazos River
drainage makes it vulnerable to
catastrophic events such as the
introduction of competitive species or
prolonged drought. State law does not
provide protection for the smalleye
shiner. The magnitude of threat is high
since the major threat of reservoir
development within the species’ current
range may render its remaining habitat
unsuitable. The threats are
nonimminent because major reservoir
projects are not likely to occur in the
near future and there is potential for
implementing other water-supply
options that could preclude reservoir
development. For these reasons, we
assigned a LPN of 5 to this species.
Zuni bluehead sucker (Catostomus
discobolus yarrowi)—The following
summary is based on information
contained in our files. No new
information was provided in the
petition we received on May 11, 2004.
The Zuni bluehead sucker is a colorful
fish less than 8 inches long. The range
of the Zuni bluehead sucker has been
reduced by over 95 percent. The Zuni
bluehead sucker currently occupies 3
river miles (4.8 kilometers) in three
headwater streams of the Rio Nutria in
New Mexico, and potentially occurs in
27.5 miles in (44 kilometers) the
Kinlichee drainage of Arizona.
However, the number of occupied miles
in Arizona is unknown and the genetic
composition of these fish is still under
investigation.
Zuni bluehead sucker range reduction
and fragmentation is caused by
discontinuous surface-water flow,
introduced species, and habitat
degradation from fine sediment
deposition. Zuni bluehead sucker
persist in very small creeks that are
subject to very low flows and drying
during periods of drought. Because of
climate change (warmer air
temperatures), stream flow is predicted
to decrease in the Southwest, even if
precipitation were to increase
moderately. Warmer winter and spring
temperatures cause an increased
fraction of precipitation to fall as rain,
resulting in a reduced snow pack, an
earlier snow melt, and a longer dry
season leading to decreased stream flow
in the summer and a longer fire season.
These changes would have a negative
effect on Zuni bluehead sucker. Another
major impact to populations of Zuni
bluehead sucker was the application of
fish toxicants through at least two dozen
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treatments in the Nutria and Pescado
rivers between 1960 and 1975. Large
numbers of Zuni bluehead suckers were
killed during these treatments. The Zuni
bluehead sucker is most likely
extirpated from Rio Pescado as none
have been collected from that river since
1993.
The New Mexico Department of Game
and Fish developed a recovery plan for
Zuni bluehead sucker which was
approved by the New Mexico State
Game Commission on December 15,
2004. The recovery plan recommends
preservation and enhancement of extant
populations and restoration of historical
Zuni bluehead sucker populations. We
predict that the recovery actions
prescribed by the recovery plan will
reduce and remove threats to this
subspecies, but they will require further
discussions and authorizations before
they can be implemented and threats are
reduced. Because of the ongoing threats
of high magnitude, including loss of
habitat (historical and current from
beaver activity), degradation of
remaining habitat (nonnative species
and land development), drought, fire,
and climate change, we maintained an
LPN of 3 for this subspecies.
Rio Grande cutthroat trout
(Oncorhynchus clarki virginalis)—The
following summary is based on
information contained in our files and
our status review published on May 14,
2008 (73 FR 27900). Rio Grande
cutthroat trout is one of 14 subspecies
of cutthroat trout found in the western
United States. Populations of this
subspecies are in New Mexico and
Colorado in drainages of the Rio Grande,
Pecos, and Canadian Rivers. Although
once widely distributed in connected
stream networks, Rio Grande cutthroat
trout populations now occupy about 10
percent of historical habitat, and the
populations are fragmented and isolated
from one another. The majority of
populations occur in high elevation
streams.
Major threats include the loss of
suitable habitat that has occurred and is
likely to continue occurring due to
water diversions, dams, stream drying,
habitat quality degradation, and changes
in hydrology, introduction of nonnative
trout and ensuing competition,
predation, and hybridization, and
whirling disease. In addition, average
air temperatures in the southwest have
increased about 1 °C (2.5 °F) in the past
30 years, and they are projected to
increase by another 1.2 to 2.8 °C (3 to
7 °F) by 2050. Because trout require cold
water, and water temperatures depend
in large part on air temperature, there is
concern that the habitat of Rio Grande
cutthroat trout will further decrease in
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response to warmer water temperatures
caused by climate change. Wildfire and
drought (stream drying) are additional
threats to Rio Grande cutthroat trout
populations that are likely to increase in
magnitude in response to climate
change. Research is occurring to assess
the effects of climate change on this
subspecies, and agencies are working to
restore historically occupied streams.
The threats are of moderate magnitude
because there is good distribution and a
comparatively large number of
populations across the landscape, some
populations have few threats present,
and in other areas management actions
are being taken to help control the threat
of nonnative trout. Overall, the threats
are ongoing and, therefore, imminent.
Based on imminent threats of moderate
magnitude, we assigned an LPN of 9 to
this subspecies.
Clams
Texas hornshell (Popenaias popei)—
The following summary is based on
information contained in our files and
information provided by the New
Mexico Department of Game and Fish
and Texas Parks and Wildlife
Department. No new information was
provided in the petition received on
May 11, 2004. The Texas hornshell is a
freshwater mussel found in the Black
River in New Mexico, and the Rio
Grande and the Devils River in Texas.
Until March 2008, the only known
extant populations were in New
Mexico’s Black River and one locality in
the Rio Grande near Laredo, Texas. In
March 2008, two new localities were
confirmed in Texas—one in the Devils
River and one in the mainstem Rio
Grande in the Rio Grande Wild and
Scenic River segment downstream of
Big Bend National Park.
The primary threats to this species are
habitat alterations such as stream bank
channelization, impoundments, and
diversions for agriculture and flood
control; contamination of water by oil
and gas activity; alterations in the
natural riverine hydrology; and
increased sedimentation and flood
pulses from prolonged overgrazing and
loss of native vegetation. Although
riverine habitats throughout the species’
known occupied range are under
constant threat from these ongoing or
potential activities, numerous
conservation actions that will benefit
the species are under way in New
Mexico, including the completion of a
State recovery plan for the species and
the drafting of a Candidate Conservation
Agreement with Assurances, and are
beginning in Texas on the Big Bend
reach of the Rio Grande. Due to these
ongoing conservation efforts, the
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magnitude of the threats is moderate.
However, the threats to the species are
ongoing, and remain imminent. Thus,
we maintained the LPN of 8 for this
species.
Fluted kidneyshell (Ptychobranchus
subtentum)—The following summary is
based on information contained in our
files. No new information was provided
in the petition we received on May 11,
2004. The fluted kidneyshell is a
freshwater mussel (Unionidae) endemic
to the Cumberland and Tennessee River
systems (Cumberlandian Region) in
Alabama, Kentucky, Tennessee, and
Virginia. It requires shoal habitats in
free-flowing rivers to survive and
successfully recruit new individuals
into its populations.
This species has been extirpated from
numerous regional streams and is no
longer found in the State of Alabama.
Habitat destruction and alteration (e.g.,
impoundments, sedimentation, and
pollutants) are the chief factors that
contributed to its decline. The fluted
kidneyshell was historically known
from at least 37 streams but is currently
restricted to no more than 12 isolated
populations. Current status information
for most of the 12 populations deemed
to be extant is available from recent
periodic sampling efforts (sometimes
annually) and other field studies,
particularly in the upper Tennessee
River system. Some populations in the
Cumberland River system have had
recent surveys as well (e.g., Wolf, Little
Rivers; Little South Fork; Horse Lick,
Buck Creeks). Populations in Buck
Creek, Little South Fork, Horse Lick
Creek, Powell River, and North Fork
Holston River have clearly declined
over the past two decades. Based on
recent information, the overall
population of the fluted kidneyshell is
declining rangewide. At this time, the
species remains in large numbers and is
viable in just the Clinch River/Copper
Creek, although smaller, viable
populations remain (e.g., Wolf, Little,
North Fork Holston Rivers; Rock Creek).
Most other populations are of
questionable or limited viability, with
some on the verge of extirpation (e.g.,
Powell River; Little South Fork; Horse
Lick, Buck, Indian Creeks). We hope
that newly reintroduced populations in
the Little Tennessee, Nolichucky, and
Duck Rivers will begin to reverse the
downward population trend of this
species. The threats are high in
magnitude, since the majority of
populations of this species are severely
affected by numerous threats
(impoundments, sedimentation, small
population size, isolation of
populations, gravel mining, municipal
pollutants, agricultural runoff, nutrient
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enrichment, and coal processing
pollution) which result in mortality or
reduced reproductive output. Since the
threats are ongoing, they are imminent.
We assigned an LPN of 2 to this mussel
species.
Neosho mucket (Lampsilis
rafinesqueana)—The following
summary is based on information
contained in our files. No new
information was provided in the
petition we received on May 11, 2004.
The Neosho mucket is a freshwater
mussel native to Arkansas, Kansas,
Missouri, and Oklahoma. The species
has been extirpated from approximately
62 percent (835 river miles (1,334 river
kilometers)) of its range. Most of this
decline has occurred in Kansas and
Oklahoma. The Neosho mucket survives
in four river drainages; however, only
one of these, the Spring River, currently
supports a relatively large population.
Significant portions of the historic
range have been inundated by the
construction of at least 11 dams.
Channel instability downstream of these
dams has further reduced suitable
habitat and mussel distribution. Range
restriction and population declines have
occurred due to habitat degradation
attributed to urbanization,
impoundments, mining, sedimentation,
and agricultural pollutants. Rapid
development and urbanization in the
Illinois River watershed will likely
continue to increase channel instability,
sedimentation, and eutrophication. The
recent rapid decline of the entire mussel
community in the Arkansas portion of
the Illinois River, including Neosho
mucket, is alarming, and it is possible
the species will be extirpated from
approximately 30 river miles (48 river
kilometers) in the very near future. The
Illinois River once represented one of
the two viable populations, but
continued viability of this stream
population is doubtful and extirpation
is imminent. The remaining extant
populations are vulnerable to random
catastrophic events (e.g., flood scour,
drought, toxic spills), land use changes
within the limited range, and genetic
isolation and the deleterious effects of
inbreeding. These threats have led to the
species being intrinsically vulnerable to
extirpation. Although state regulations
limit harvest of this species, there is
little protection for habitat. The threats
are high in magnitude as they occur
throughout the range of this species, and
the majority of these threats are ongoing
and imminent. Thus, we assigned a
listing priority number of 2 to this
species.
Alabama pearlshell (Margaritifera
marrianae)—We continue to find that
listing this species is warranted but
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precluded as of the date of publication
of this notice. However, we are working
on a proposed listing rule that we
expect to publish prior to making the
next annual resubmitted 12-month
petition finding.
Slabside pearlymussel (Lexingtonia
dolabelloides)—The following summary
is based on information contained in
our files. No new information was
provided in the petition we received on
May 11, 2004. The slabside
pearlymussel is a freshwater mussel
(Unionidae) endemic to the Cumberland
and Tennessee River systems
(Cumberlandian Region) in Alabama,
Kentucky, Tennessee, and Virginia. It
requires shoal habitats in free-flowing
rivers to survive and successfully recruit
new individuals into its populations.
Habitat destruction and alteration
(e.g., impoundments, sedimentation,
and pollutants) are the chief factors
contributing to the decline of this
species, which has been extirpated from
numerous regional streams and is no
longer found in Kentucky. The slabside
pearlymussel was historically known
from at least 32 streams, but is currently
restricted to no more than 10 isolated
stream segments. Current status
information for most of the 10
populations deemed to be extant is
available from recent periodic sampling
efforts (sometimes annually) and other
field studies. Comprehensive surveys
have taken place in the Middle and
North Forks Holston River, Paint Rock
River, and Duck River in the past
several years. Based on recent
information, the overall population of
the slabside pearlymussel is declining
rangewide. Of the five streams in which
the species remains in good numbers
(e.g., Clinch, North and Middle Forks
Holston, Paint Rock, Duck Rivers), the
Middle and upper North Fork Holston
Rivers have undergone drastic recent
declines, while the Clinch population
has been in a longer-term decline. Most
of the remaining five populations (e.g.,
Powell River, Big Moccasin Creek,
Hiwassee River, Elk River, Bear Creek)
have doubtful viability, and several if
not all of them may be on the verge of
extirpation.
The threats remain high in magnitude,
since all populations of this species are
severely affected in numerous ways
(impoundments, sedimentation, small
population size, isolation of
populations, gravel mining, municipal
pollutants, agricultural runoff, nutrient
enrichment, and coal processing
pollution) which result in mortality or
reduced reproductive output leading to
a relatively high likelihood of
extinction. We assigned an LPN of 2 to
this mussel species.
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Snails
Phantom Cave snail (Cochliopa
texana) and Phantom springsnail
(Tryonia cheatumi)—The following
summary is based on information
contained in our files. No new
information was provided in the
petition we received on May 11, 2004.
Phantom Cave snail and Phantom
springsnail are small aquatic snails that
occur in three spring outflows in the
Toyah Basin in Reeves and Jeff Davis
Counties, Texas.
The primary threat to both species is
the loss of surface flows due to
declining groundwater levels from
drought, pumping for agricultural
production, and potentially climate
change. Much of the land immediately
surrounding their spring habitat is
owned and managed by The Nature
Conservancy, Bureau of Reclamation,
and Texas Parks and Wildlife
Department. However, the water needed
to maintain their habitat has declined
due to a reduction in spring flows,
possibly as a result of private
groundwater pumping in areas beyond
that controlled by these landowners. As
an example, Phantom Lake Spring, one
of the sites of occurrence, has already
ceased flowing and aquatic habitat is
artificially supported only by a pumping
system. The magnitude of the threats is
high because spring flow loss would
result in complete habitat destruction
and permanent elimination of all
populations of the species. The
immediacy of the threats is imminent,
as evidenced by the drastic decline in
spring flow at Phantom Lake Spring that
is currently happening and may
extirpate these populations in the near
future. Declining spring flows in San
Solomon Spring are also becoming
evident and will affect that spring site
as well within the foreseeable future.
Thus, we maintained the LPN of 2 for
both species.
Sisi snail (Ostodes strigatus)—The
following summary is based on
information contained in our files. No
new information was provided in the
petition we received on May 11, 2004.
The sisi snail is a ground-dwelling
species in the Potaridae family, and is
endemic to American Samoa. The
species is now known from a single
population on the island of Tutuila,
American Samoa.
This species is currently threatened
by habitat loss and modification and by
predation from nonnative predatory
snails. The decline of the sisi in
American Samoa has resulted, in part,
from loss of habitat to forestry and
agriculture and loss of forest structure to
hurricanes and alien weeds that
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establish after these storms. All live sisi
snails have been found in the leaf litter
beneath remaining intact forest canopy.
No snails were found in areas bordering
agricultural plots or in forest areas that
were severely damaged by three
hurricanes (1987, 1990, and 1991).
Under natural historical conditions, loss
of forest canopy to storms did not pose
a great threat to the long-term survival
of these snails; enough intact forest with
healthy populations of snails would
support dispersal back into newly
regrown canopy forest. However, the
presence of alien weeds such as mile-aminute vine (Mikania micrantha) may
reduce the likelihood that native forest
will re-establish in areas damaged by
the hurricanes. This loss of habitat to
storms is greatly exacerbated by
expanding agriculture. Agricultural
plots on Tutuila have spread from low
elevation up to middle and some high
elevations, greatly reducing the forest
area and thus reducing the resilience of
native forests and its populations of
native snails. These reductions also
increase the likelihood that future
storms will lead to the extinction of
populations or species that rely on the
remaining canopy forest. In an effort to
eradicate the giant African snail
(Achatina fulica), the alien rosy
carnivore snail (Euglandia rosea) was
introduced in 1980. The rosy carnivore
snail has spread throughout the main
island of Tutuila. Numerous studies
show that the rosy carnivore snail feeds
on endemic island snails including the
sisi, and is a major agent in their
declines and extirpations. At present,
the major threat to long-term survival of
the native snail fauna in American
Samoa is predation by nonnative
predatory snails. These threats are
ongoing and are therefore imminent.
Since the threats occur throughout the
entire range of the species, have a severe
effect on the survival of the snails,
leading to a relatively high likelihood of
extinction, they are of a high magnitude.
Therefore we assigned this species an
LPN of 2.
Diamond Y Spring snail
(Pseudotryonia adamantina) and
Gonzales springsnail (Tryonia
circumstriata)—The following summary
is based on information contained in
our files. No new information was
provided in the petition we received on
May 11, 2004. Diamond Y Spring snail
and Gonzales springsnail are small
aquatic snails endemic to Diamond Y
Spring in Pecos County, Texas. The land
surrounding the spring and its outflow
channels are owned and managed by
The Nature Conservancy.
These snails are primarily threatened
with habitat loss due to springflow
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declines from drought, pumping of
groundwater, and potentially of climate
change. Additional threats include
water contamination from accidental
releases of petroleum products, as their
habitat is in an active oil and gas field.
Also, a nonnative aquatic snail
(Melanoides sp.) was introduced into
the native snails’ habitat and may
compete with endemic snails for space
and resources. The magnitude of threats
is high because limited distribution of
these narrow endemics makes any
impact from increasing threats (e.g., loss
of springflow, contaminants, and
nonnative species) likely to result in the
extinction of the species. These species
occur in one location in an arid region
currently plagued by drought and
ongoing aquifer withdrawals, making
the eventual loss of spring flow an
imminent threat of total habitat loss.
Thus, we maintained the LPN of 2 for
both species.
Fragile tree snail (Samoana fragilis)—
The following summary is based on
information contained in our files. No
new information was provided in the
petition we received on May 11, 2004.
A tree-dwelling species, the fragile tree
snail is a member of the Partulidae
family of snails, and is endemic to the
islands of Guam and Rota (Mariana
Islands). Requiring cool and shaded
native forest habitat, the species is now
known from one population on Guam
and from one population on Rota.
This species is currently threatened
by habitat loss and modification and by
predation from nonnative predatory
snails and flatworms. Large numbers of
Philippine deer (Cervus mariannus)
(Guam and Rota), pigs (Sus scrofra)
(Guam), water buffalo (Bubalus bubalis)
(Guam), and cattle (Bos taurus) (Rota)
directly alter the understory plant
community and overall forest
microclimate, making it unsuitable for
snails. Predation by the alien rosy
carnivore snail (Euglandina rosea) and
the Manokwar flatworm (Platydemus
manokwari) is a serious threat to the
survival of the fragile tree snail. Field
observations have established that the
rosy carnivore snail and the Manokwar
flatworm will readily feed on native
Pacific island tree snails, including the
Partulidae, such as those of the Mariana
Islands. The rosy carnivore snail has
caused the extirpation of many
populations and species of native snails
throughout the Pacific islands. The
Manokwar flatworm has also
contributed to the decline of native tree
snails, in part due to its ability to ascend
into trees and bushes that support
native snails. Areas with populations of
the flatworm usually lack partulid tree
snails or have declining numbers of
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snails. Because all of the threats occur
rangewide, have a significant effect on
the survival of this snail species, leading
to a relatively high likelihood of
extinction, they are high in magnitude.
The threats are also ongoing and thus
are imminent. Therefore, we assigned
this species an LPN of 2.
Guam tree snail (Partula radiolata)—
The following summary is based on
information contained in our files. No
new information was provided in the
petition we received on May 11, 2004.
A tree-dwelling species, the Guam tree
snail is a member of the Partulidae
family of snails and is endemic to the
island of Guam. Requiring cool and
shaded native forest habitat, the species
is now known from 22 populations on
Guam.
This species is primarily threatened
by predation from nonnative predatory
snails and flatworms. In addition, the
species is also threatened by habitat loss
and degradation. Predation by the alien
rosy carnivore snail (Euglandina rosea)
and the alien Manokwar flatworm
(Platydemus manokwari) is a serious
threat to the survival of the Guam tree
snail (see summary for the fragile tree
snail, above). On Guam, open
agricultural fields and other areas prone
to erosion were seeded with
tangantangan (Leucaena leucocephala)
by the U.S. Military. Tangantangan
grows as a single species stand with no
substantial understory. The
microclimatic condition is dry with
little accumulation of leaf litter humus
and is particularly unsuitable as Guam
tree snail habitat. In addition, native
forest cannot reestablish and grow
where this alien weed has become
established. Because all of the threats
occur rangewide, have a significant
effect on the survival of this snail
species, leading to a relatively high
likelihood of extinction, they are high in
magnitude. The threats are also ongoing
and thus are imminent. Therefore, we
assigned this species an LPN of 2.
Humped tree snail (Partula gibba)—
The following summary is based on
information contained in our files. No
new information was provided in the
petition we received on May 11, 2004.
A tree-dwelling species, the humped
tree snail is a member of the Partulidae
family of snails, and was originally
known from the island of Guam and the
Commonwealth of the Northern Mariana
Islands (islands of Rota, Aguiguan,
Tinian, Saipan, Anatahan, Sarigan,
Alamagan, and Pagan). Most recent
surveys revealed a total of 13
populations on the islands of Guam,
Rota, Aguiguan, Sarigan, Saipan,
Alamagan, and Pagan. Although still the
most widely distributed tree snail
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endemic in the Mariana Islands,
remaining population sizes are often
small.
This species is currently threatened
by habitat loss and modification and by
predation from nonnative predatory
snails and flat worms. Throughout the
Mariana Islands, feral ungulates (pigs
(Sus scrofa), Philippine deer (Cervus
mariannus), cattle (Bos taurus), water
buffalo (Bubalus bubalis), and goats
(Capra hircus)) have caused severe
damage to native forest vegetation by
browsing directly on plants, causing
erosion, and retarding forest growth and
regeneration. This in turn reduces the
quantity and quality of forested habitat
for the humped tree snail. Currently,
populations of feral ungulates are found
on the islands of Guam (deer, pigs, and
water buffalo), Rota (deer and cattle),
Aguiguan (goats), Saipan (deer, pigs,
and cattle), Alamagan (goats, pigs, and
cattle), and Pagan (cattle, goats, and
pigs). Goats were eradicated from
Sarigan in 1998 and the humped tree
snail has increased in abundance on
that island, likely in response to the
removal of all the goats. However, the
population of humped tree snails on
Anatahan is likely extirpated due to the
massive volcanic explosions of the
island beginning in 2003 and still
continuing, and the resulting loss of up
to 95 percent of the vegetation on the
island. Predation by the alien rosy
carnivore snail (Euglandina rosea) and
the alien Manokwar flatworm
(Platydemus manokwari) is a serious
threat to the survival of the humped tree
snail (see summary for the fragile tree
snail, above). The magnitude of threats
is high because these alien predators
cause significant population declines to
the humped tree snail rangewide. These
threats are ongoing and thus are
imminent. Therefore, we assigned this
species an LPN of 2.
Lanai tree snail (Partulina
semicarinata)—We continue to find that
listing this species is warranted but
precluded as of the date of publication
of this notice. However, we are working
on a proposed listing rule that we
expect to publish prior to making the
next annual resubmitted petition
12-month finding.
Lanai tree snail (Partulina
variabilis)—We continue to find that
listing this species is warranted but
precluded as of the date of publication
of this notice. However, we are working
on a proposed listing rule that we
expect to publish prior to making the
next annual resubmitted petition
12-month finding.
Langford’s tree snail (Partula
langfordi)—The following summary is
based on information contained in our
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files. No new information was provided
in the petition we received on May 11,
2004. A tree-dwelling species,
Langford’s tree snail is a member of the
Partulidae family of snails, and is
known from one population on the
island of Aguiguan.
This species is currently threatened
by habitat loss and modification and by
predation from nonnative predatory
snails. In the 1930s, the island of
Aguiguan was mostly cleared of native
forest to support sugar cane and
pineapple production. The abandoned
fields and airstrip are now overgrown
with alien weeds. The remaining native
forest understory has greatly suffered
from large and uncontrolled populations
of alien goats and the invasion of weeds.
Goats (Capra hircus) have caused severe
damage to native forest vegetation by
browsing directly on plants, causing
erosion, and retarding forest growth and
regeneration. This in turn reduces the
quantity and quality of forested habitat
for Langford’s tree snail. Predation by
the alien rosy carnivore snail
(Euglandina rosea) and by the
Manokwar flatworm (Platydemus
manokwari) (see summary for the fragile
tree snail, above) is also a serious threat
to the survival of Langford’s tree snail.
All of the threats are occurring
rangewide and no efforts to control or
eradicate the nonnative predatory snail
species or to reduce habitat loss are
being undertaken. The magnitude of
threats is high because they result in
direct mortality or significant
population declines to Langford’s tree
snail rangewide. A survey of Aguiguan
in November 2006 failed to find any live
Langford’s tree snails. These threats are
also ongoing and thus are imminent.
Therefore, we assigned this species an
LPN of 2.
Newcomb’s tree snail (Newcombia
cumingi)—We continue to find that
listing this species is warranted but
precluded as of the date of publication
of this notice. However, we are working
on a proposed listing rule that we
expect to publish prior to making the
next annual resubmitted petition 12month finding.
Tutuila tree snail (Eua zebrina)—The
following summary is based on
information contained in our files. No
new information was provided in the
petition we received on May 11, 2004.
A tree-dwelling species, the Tutuila tree
snail is a member of the Partulidae
family of snails, and is endemic to
American Samoa. The species is known
from 32 populations on the islands of
Tutuila, Nuusetoga, and Ofu.
This species is currently threatened
by habitat loss and modification and by
predation from nonnative predatory
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snails and rats. All live Tutuila tree
snails were found on understory
vegetation beneath remaining intact
forest canopy. No snails were found in
areas bordering agricultural plots or in
forest areas that were severely damaged
by three hurricanes (1987, 1990, and
1991). (See summary for the sisi snail,
above, regarding impacts of alien weeds
and of the rosy carnivore snail.) Rats
(Rattus spp) have also been shown to
devastate snail populations, and ratchewed snail shells have been found at
sites where the Tutuila snail occurs. At
present, the major threat to the longterm survival of the native snail fauna
in American Samoa is predation by
nonnative predatory snails and rats. The
magnitude of threats is high because
they result in direct mortality or
significant population declines to the
Tutuila tree snail rangewide. The threats
are also ongoing and thus are imminent.
Therefore, we assigned this species an
LPN of 2.
Chupadera springsnail (Pyrgulopsis
chupaderae)—We continue to find that
listing this species is warranted but
precluded as of the date of publication
of this notice. However, we are working
on a proposed listing rule that we
expect to publish prior to making the
next annual resubmitted petition
12-month finding.
Elongate mud meadows springsnail
(Pyrgulopsis notidicola)—The following
summary is based on information
contained in our files. No new
information was provided in the
petition received on May 11, 2004.
Pyrgulopsis notidicola is endemic to
Soldier Meadow, which is located at the
northern extreme of the western arm of
the Black Rock Desert in the transition
zone between the Basin and Range
Physiographic Province and the
Columbia Plateau Province, Humboldt
County, Nevada. The type locality, and
the only known location of the species,
occurs in four separate stretches of
thermal (between 45° and 32° Celsius,
113° and 90° Fahrenheit) aquatic
habitat. The first stretch is the largest at
approximately 600 m (1,968 ft) long and
2 m (6.7 ft) wide. The other stretches
where P. notidicola occurs are less than
6 m (19.7 ft) long and 0.5 m (1.6 ft)
wide. Pyrgulopsis notidicola occurs
only in shallow, flowing water on gravel
substrate. The species does not occur in
deep water (i.e., impoundments) where
water velocity is low, gravel substrate is
absent, and sediment levels are high.
The species and its habitat are
threatened by recreational use in the
areas where it occurs as well as the
ongoing impacts of past water
diversions and livestock grazing and
current off-highway vehicle travel.
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Conservation measures implemented by
the Bureau of Land Management
include the installation of fencing to
exclude livestock, wild horses, burros
and other large mammals; closing of
access roads to spring, riparian, and
wetland areas and the limiting of
vehicles to designated routes; the
establishment of a designated
campground away from the habitats of
sensitive species; the installation of
educational signage; and, increased staff
presence, including law enforcement
and a volunteer site steward during the
6-month period of peak visitor use.
These conservation measures have
reduced the magnitude of threat to the
species to moderate to low; all
remaining threats are nonimminent and
involve long-term changes to the habitat
for the species resulting from past
impacts. Until a monitoring program is
in place that allows us to assess the
long-term trend of the species, we have
assigned an LPN of 11.
Gila springsnail (Pyrgulopsis gilae)—
The following summary is based on
information contained in our files and
the petition we received on November
20, 1985. Also see our 12-month
petition finding published in the
Federal Register on October 4, 1988 (53
FR 38969). The Gila springsnail is an
aquatic species known from 13
populations in New Mexico. Surveys
conducted in 2008 and 2009 located 14
additional populations bringing the total
known to 27. Given the new population
information, as well as new information
on threats, we are currently assessing
the status of this species.
The long-term persistence of the Gila
springsnail is contingent upon
protection of the riparian corridor and
maintenance of flow to ensure
continuous, oxygenated flowing water
within the species’ required thermal
range. Occupied Gila springsnail
localities on Federal lands surveyed in
2008 and 2009 are subject to light levels
of recreational use only at the thermal
springs, and overall, recreational
activities do not appear to be affecting
springsnail populations. The level of
recreational impacts at thermal springs
on private lands is unknown. Sites
visited in 2008 were excluded from
grazing. Although elk use at some of the
springs was evident, the level of impact
was low. Of greatest concern are the
very small size of the isolated occupied
habitats and the potential effects of
climate change. Although the effect
climate change will have on the springs
of the Southwest is unpredictable, mean
annual temperature in New Mexico has
increased by 0.6 degrees per decade
since 1970. Higher temperatures lead to
higher evaporation rates, increased
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evapotranspiration, and decreased soil
moisture which may reduce the amount
of groundwater recharge. Widespread,
long-term drought could affect spring
flow quantity and quality, negatively
affecting the springsnail populations.
Based on these nonimminent threats
that are currently of a low magnitude,
we retained a listing priority number of
11 for this species.
Gonzales springsnail (Tryonia
circumstriata)—See summary above
under Diamond Y Spring snail
(Pseudotryonia adamantina).
Huachuca springsnail (Pyrgulopsis
thompsoni)—The following is based on
information contained in our files. No
new information was provided in the
petition we received on May 11, 2004.
The Huachuca springsnail inhabits
approximately 16 springs and cienegas
at elevations of 4,500 to 7,200 feet in
southeastern Arizona (14 sites) and
adjacent portions of Sonora, Mexico (2
sites). The springsnail is typically found
in the shallower areas of springs or
cienegas, often in rocky seeps at the
spring source. Ongoing threats include
habitat modification and destruction
through catastrophic wildfire; drought;
streamflow alteration; and, potentially,
grazing, recreation, military activities,
and timber harvest. Overall, the threats
are moderate in magnitude because
threats are not occurring throughout the
range of the species uniformly and not
all populations would likely be affected
simultaneously by any of the known
threats. In addition, multiple
landowners (U.S. Forest Service, Fort
Huachuca, and The Nature
Conservancy) are including
consideration for the springsnail or
other co-occurring listed species in their
activities (reducing fuel loads, avoiding
occupied sites during military
operations). The threats are ongoing
and, thus, imminent. Therefore, we have
assigned an LPN of 8 to this species.
New Mexico springsnail (Pyrgulopsis
thermalis)—The following summary is
based on information contained in our
files and the petition received on
November 20, 1985. Also see our 12month petition finding published on
October 4, 1988 (53 FR 38969). In
addition, we have received new
information on populations and threats
to the species, which we are currently
assessing. The New Mexico springsnail
is an aquatic species known from twelve
separate populations associated with a
series of spring-brook systems along the
Gila River in the Gila National Forest in
Grant County, New Mexico.
The long-term persistence of the New
Mexico springsnail is contingent upon
protection of the riparian corridor
immediately adjacent to springhead and
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springrun habitats. Although the New
Mexico springsnail populations may be
stable, the sites inhabited by the species
are subject to levels of recreational use
and livestock grazing that can negatively
affect this species. If these uses remain
at the current or lower levels, they will
not pose an imminent threat to the
species. Of greater concern is drought,
which could affect spring discharge and
increases the potential for fire. Although
the effect global climate change may
have on streams and forests of the
Southwest is unpredictable, mean
annual temperature in New Mexico has
increased by 0.6 degrees per decade
since 1970. Higher temperatures lead to
higher evaporation rates which may
reduce the amount of runoff and
groundwater recharge. Increased
temperatures may also increase the
extent of area influenced by drought and
fire. Large fires have occurred in the
Gila National Forest and subsequent
floods and ash flows have severely
affected aquatic life in streams. If the
drought continues or worsens, the
imminence of threats from decreased
discharge and fire will increase. Based
on these nonimminent threats of a low
magnitude, we retain an LPN of 11 for
this springsnail.
Page springsnail (Pyrgulopsis
morrisoni)—See above in ‘‘Listing
Priority Changes in Candidates.’’ The
above summary is based on information
contained in our files.
Phantom springsnail (Tyronia
cheatumi)—See summary above under
Phantom Cave snail (Cochliopa texana).
Three Forks springsnail (Pyrgulopsis
trivialis)—We continue to find that
listing this species is warranted but
precluded as of the date of publication
of this notice. However, we are working
on a proposed listing rule that we
expect to publish prior to making the
next annual resubmitted petition 12month finding.
Insects
Wekiu bug (Nysius wekiuicola)—The
following summary is based on
information contained in our files. No
new information was provided in the
petition we received on May 11, 2004.
The wekiu bug belongs to the true bug
family, Lygaeidae, and is endemic to the
island of Hawaii. This species only
occurs on the summit of Mauna Kea and
feeds upon other insect species which
are blown to the summit of this large
volcano. The wekiu bug is primarily
threatened by the loss of its habitat from
astronomy development. In 2004 and
early 2005, surveys found multiple new
locations of the wekiu bug on cinder
cones on the Mauna Kea summit.
Several of these cinder cones within the
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Mauna Kea Science Reserve, as well as
two cinder cones located in the State Ice
Age Natural Area Reserve, are not
currently undergoing development nor
are they the site of any planned
development. Thus, the threats,
although ongoing, do not occur across
the entire range of the wekiu bug.
Because there are occupied locations
that are not subject to the primary threat
of astronomy development, the overall
magnitude of the threat is moderate. The
immediacy of the threats is imminent
because there are still significant parts
of the wekiu bug’s range where
development is occurring. Therefore, we
assigned this species an LPN of 8.
Mariana eight spot butterfly
(Hypolimnas octucula mariannensis)—
The following summary is based on
information contained in our files. No
new information was provided in the
petition we received on May 11, 2004.
The Mariana eight spot butterfly is a
nymphalid butterfly species that feeds
upon two host plants, Procris
pedunculata and Elatostema calcareum.
Endemic to the islands of Guam and
Saipan, the species is now known from
ten populations on Guam. This species
is currently threatened by predation and
parasitism. The Mariana eight spot
butterfly has extremely high mortality of
eggs and larvae due to predation by
alien ants and wasps. Because the threat
of parasitism and predation by
nonnative insects occurs rangewide and
can cause significant population
declines to this species, they are high in
magnitude. The threats are imminent
because they are ongoing. Therefore, we
assigned an LPN of 3 for this subspecies.
Mariana wandering butterfly (Vagrans
egestina)—The following summary is
based on information contained in our
files. No new information was provided
in the petition we received on May 11,
2004. The Mariana wandering butterfly
is a nymphalid butterfly species which
feeds upon a single host plant species,
Maytenus thompsonii. Originally known
from and endemic to the islands of
Guam and Rota, the species is now
known from one population on Rota.
This species is currently threatened by
alien predation and parasitism. The
Mariana wandering butterfly is likely
predated by alien ants and parasitized
by native and nonnative parasitoids.
Because the threats of parasitism and
predation by nonnative insects occur
rangewide and can cause significant
population declines to this species,
leading to a relatively high likelihood of
extinction, they are high in magnitude.
These threats are imminent because
they are ongoing. Therefore, we
assigned an LPN of 2 for this species.
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Miami blue butterfly (Cyclargus
thomasi bethunebakeri)—The following
summary is based on information
contained in our files and in the petition
we received on June 15, 2000.
Historically, the Miami blue was most
common on the south Florida mainland
and the Florida Keys, with a range
extending north to Hillsborough and
Volusia Counties. It is presently located
at two sites in the Keys. In 1999, a
metapopulation was discovered at Bahia
Honda State Park (BHSP) on Bahia
Honda Key, and in 2006 a second
metapopulation was discovered on the
outer islands of Key West National
Wildlife Refuge (KWNWR). The BHSP
metapopulation appears restricted to a
couple hundred individuals at most; the
KWNWR metapopulation was believed
to be several hundred in 2006–2007, but
appears to be lower in abundance now.
Capacity to expand at either site or
successfully emigrate from either site
appears to be very low due to the
sedentary nature of the butterfly and
isolation of habitats. Reintroduction
efforts have not been successful. The
Miami blue is predominantly a coastal
species, occurring in disturbed and
early successional habitats such as the
edges of tropical hardwood hammock,
coastal berm forest, coastal prairie, and
along trails and other open sunny areas,
and historically in pine rockland. These
habitats provide hostplants for larvae
and nectar sources for adults in close
proximity, as the species requires.
Major threats to the butterfly include
few occurrences, limited population
size and range, hurricanes, mosquito
control activities, and herbivory of
hostplants by iguanas. Damage to host
plants from iguanas at BHSP is an
ongoing and significant threat; although
active steps are being taken by the State
and partners to reduce this threat, this
metapopulation is now at risk. Climatic
changes and sea level rise are long-term
threats that will reduce the extent of
habitat. Accidental harm or habitat
destruction and illegal collection may
also pose threats to the survival due to
small population sizes. Loss of genetic
diversity within the small and isolated
populations may be occurring. The
survival of the Miami blue depends on
protecting the species’ currently
occupied habitat from further
degradation and fragmentation;
restoring potentially suitable habitat
within its historical range; avoiding or
removing threats from fire suppression,
iguanas, mosquito control, accidental
harm from humans; increasing the
current population in size; and
establishing populations at other
locations. Exotic predatory ants and
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parasitoids may also be potential
threats, given the species’ small
population size and few occurrences.
Most threats are high in magnitude,
because they constitute a significant risk
to the subspecies, leading to a relatively
high likelihood of extinction; most
threats are imminent. As a result, we
retained an LPN of 3 for this subspecies.
Sequatchie caddisfly (Glyphopsyche
sequatchie)—The following summary is
based on information in our files. No
new information was provided in the
petition we received on May 11, 2004.
The Sequatchie caddisfly is known from
two spring runs that emerge from caves
in Marion County, Tennessee—Owen
Spring Branch (the type locality) and
Martin Spring run in the Battle Creek
system. In 1998, biologists estimated
population sizes at 500 to 5,000
individuals for Owen Spring Branch
and 2 to 10 times higher at Martin
Spring, due to the greater amount of
apparently suitable habitat. In spite of
greater amounts of suitable habitat at the
Martin Spring run, Sequatchie
caddisflies are more difficult to find at
this site, and in 2001 (the most recent
survey) the Sequatchie caddisfly was
‘‘abundant’’ at the Owen Spring Branch
location, while only two individuals
were observed at the Martin Spring.
Threats to the Sequatchie caddisfly
include siltation, point and nonpoint
discharges from municipal and
industrial activities, and introduction of
toxicants during episodic events. These
threats, coupled with the extremely
limited distribution of the species, its
apparent small population size, the
limited amount of occupied habitat,
ease of accessibility, and the annual life
cycle of the species, are all factors that
leave the Sequatchie caddisfly
vulnerable to extirpation. Therefore, the
magnitude of the threat is high. These
threats are gradual and not necessarily
imminent. Based on high-magnitude,
nonimminent threats, we assigned this
species a listing priority number of 5.
Clifton Cave beetle
(Pseudanophthalmus caecus)—The
following summary is based upon
information contained in our files. No
new information was provided in the
petition we received on May 11, 2004.
Clifton Cave beetle is a small, eyeless,
reddish-brown predatory insect that
feeds upon small cave invertebrates. It
is cave dependent, and is not found
outside the cave environment. Clifton
Cave beetle is only known from two
privately owned Kentucky caves. Soon
after the species was first collected in
1963 in one cave, the cave entrance was
enclosed due to road construction. We
do not know whether the species still
occurs at the original location or if it has
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been extirpated from the site by the
closure of the cave entrance. Other
caves in the vicinity of this cave were
surveyed for the species during 1995 to
1996 and only one additional site was
found to support the Clifton Cave beetle.
The limestone caves in which the
Clifton Cave beetle is found provide a
unique and fragile environment that
supports a variety of species that have
evolved to survive and reproduce under
the demanding conditions found in cave
ecosystems. The limited distribution of
the species makes it vulnerable to
isolated events that would only have a
minimal effect on the more wideranging insects. Events such as toxic
chemical spills, discharges of large
amounts of polluted water or indirect
impacts from off-site construction
activities, closure of entrances,
alteration of entrances, or the creation of
new entrances could have serious
adverse impacts on this species.
Therefore, the magnitude of threat is
high for this species. The threats are
nonimminent because there are no
known projects planned that would
affect the species in the near future. We
therefore have assigned a listing priority
number of 5 to this species.
Icebox Cave beetle
(Pseudanophthalmus frigidus)—The
following summary is based upon
information contained in our files. No
new information was provided in the
petition we received on May 11, 2004.
Icebox Cave beetle is a small, eyeless,
reddish-brown predatory insect that
feeds upon small cave invertebrates. It
is not found outside the cave
environment, and is only known from
one privately owned Kentucky cave.
The limestone cave in which this
species is found provides a unique and
fragile environment that supports a
variety of species that have evolved to
survive and reproduce under the
demanding conditions found in cave
ecosystems. The species has not been
observed since it was originally
collected, but species experts believe
that it may still exist in the cave in low
numbers. The limited distribution of the
species makes it vulnerable to isolated
events that would only have a minimal
effect on the more wide-ranging insects.
Events such as toxic chemical spills or
discharges of large amounts of polluted
water, or indirect impacts from off-site
construction activities, closure of
entrances, alteration of entrances, or the
creation of new entrances, could have
serious adverse impacts on this species.
Therefore, the magnitude of threat is
high for this species because it is
limited in distribution and the threats
would result in a high level of mortality
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or reduced reproductive capacity. The
threats are nonimminent because there
are no known projects planned that
would affect the species in the near
future. We therefore have assigned an
LPN of 5 to this species.
Inquirer Cave beetle
(Pseudanophthalmus inquisitor)—The
following summary is based upon
information contained in our files. No
new information was provided in the
petition we received on May 11, 2004.
The Inquirer Cave beetle is a fairly
small, eyeless, reddish-brown predatory
insect that feeds upon small cave
invertebrates. It is not found outside the
cave environment, and is only known
from one privately owned Tennessee
cave. The limestone cave in which this
species is found provides a unique and
fragile environment that supports a
variety of species that have evolved to
survive and reproduce under the
demanding conditions found in cave
ecosystems. The species was last
observed in 2006. The limited
distribution of the species makes it
vulnerable to isolated events that would
only have a minimal effect on the more
wide-ranging insects. The area around
the only known site for the species is in
a rapidly expanding urban area. The
entrance to the cave is protected by the
landowner through a cooperative
management agreement with the
Service, The Nature Conservancy and
Tennessee Wildlife Resources Agency;
however, a sinkhole that drains into the
cave system is located away from the
protected entrance and is near a
highway. Events such as toxic chemical
spills, discharges of large amounts of
polluted water, or indirect impacts from
off-site construction activities, could
severely affect the species and the cave
habitat. The magnitude of threat is high
for this species because it is limited in
distribution and the threats would have
severe impacts on its continued
existence. The threats are nonimminent
because there are no known projects
planned that would affect the species in
the near future and it receives some
protection under a cooperative
management agreement. We therefore
have assigned a listing priority number
of 5 to this species.
Louisville Cave beetle
(Pseudanophthalmus troglodytes)—The
following summary is based upon
information contained in our files. No
new information was provided in the
petition we received on May 11, 2004.
The Louisville Cave beetle is a small,
eyeless, reddish-brown predatory insect
that feeds upon cave invertebrates. It is
not found outside the cave environment,
and is only known from two privately
owned Kentucky caves. The limestone
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caves in which this species is found
provide a unique and fragile
environment that supports a variety of
species that have evolved to survive and
reproduce under the demanding
conditions found in cave ecosystems.
The limited distribution of the species
makes it vulnerable to isolated events
that would only have a minimal effect
on the more wide-ranging insects.
Events such as toxic chemical spills,
discharges of large amounts of polluted
water or indirect impacts from off-site
construction activities, closure of
entrances, alteration of entrances, or the
creation of new entrances could have
serious adverse impacts on this species.
The magnitude of threat is high for this
species, because it is limited in
distribution and the threats would have
severe negative impacts on the species.
The threats are nonimminent because
there are no known projects planned
that would affect the species in the near
future. We therefore have assigned an
LPN of 5 to this species.
Tatum Cave beetle
(Pseudanophthalmus parvus)—The
following summary is based upon
information contained in our files. No
new information was provided in the
petition we received on May 11, 2004.
Tatum Cave beetle is a small, eyeless,
reddish-brown predatory insect that
feeds upon cave invertebrates. It is not
found outside the cave environment,
and is only known from one privately
owned Kentucky cave. The limestone
cave in which this species is found
provides a unique and fragile
environment that supports a variety of
species that have evolved to survive and
reproduce under the demanding
conditions found in cave ecosystems.
The species has not been observed since
1965, but species experts believe that it
still exists in low numbers. The limited
distribution of the species makes it
vulnerable to isolated events that would
only have a minimal effect on the more
wide-ranging insects. Events such as
toxic chemical spills or discharges of
large amounts of polluted water, or
indirect impacts from off-site
construction activities, closure of
entrances, alteration of entrances, or the
creation of new entrances could have
serious adverse impacts on this species.
The magnitude of threat is high for this
species, because its limited numbers
mean that any threats could severely
affect its continued existence. The
threats are nonimminent because there
are no known projects planned that
would affect the species in the near
future. We therefore have assigned an
LPN of 5 to this species.
Taylor’s (Whulge, Edith’s)
checkerspot butterfly (Euphydryas
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editha taylori)—The following summary
is based on information contained in
our files and in the petition received on
December 11, 2002. Historically, the
Taylor’s checkerspot butterfly was
known from 70 locations: 23 in British
Columbia, 34 in Washington, and 13 in
Oregon. Based on the results of surveys
during the 2009 flight period, butterflies
were detected at just 9 populations. No
reports were received for the Canada
sites. The total number of Taylor’s
checkerspot butterflies was considerably
reduced in current surveys with
approximately 2,500 individuals
observed rangewide. The latest decline
observed was from the Joint Base Lewis
McChord population where fewer than
200 butterflies were counted in 2008;
only 77 adult butterflies were detected
during 2009 surveys. Currently, just
seven populations had adult butterflies
flying in Washington, two in the
Willamette Valley of Oregon, and one
on Denman Island, British Columbia,
Canada. A new population (metapopulation) was observed on the
Olympic National Forest. During 2009,
six additional locations have been found
on suitable habitat on Olympic National
Forest land; at one location 69
butterflies were detected and the
remainder had up to 40 butterflies with
several of the sites having fewer than
5 adult butterflies.
Threats include degradation and
destruction of native grasslands due to
agriculture; residential and commercial
development; encroachment by
nonnative plants; succession from
grasslands to native shrubs and trees;
and fire. The threat of military training
has greatly increased during this last
assessment period and the site where
Taylor’s checkerspot were known to
thrive on Fort Lewis was severely
affected by Armored Vehicle training.
The result of that training on the
population at the site will not be
determined until after this year’s
monitoring has been completed.
The grassland ecosystem on which
this subspecies depends requires annual
management to maintain suitable
grassland habitat for the species.
Bacillus thuringiensis var. kurstake
(Btk) was routinely applied for Asian
gypsy moth control in Pierce County,
Washington for many years. This
pesticide is documented to have
deleterious effects on non-target
lepidopteron species, including all
moths and butterflies. Because of the
timing and close proximity of the Btk
application to native prairies where
Taylors’ checkerspot adults, or their
larvae, were historically known to
occur, it is likely that the spraying
contributed to the extirpation of the
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subspecies at three locations in Pierce
County, Washington.
Threats also include the loss of
prairies to development or the
conversion of native grasslands to
agriculture; the threat of vehicle and
foot traffic that crushes larvae and larval
host plants on roads where host plants
have become established, thus acting as
a mortality sink (this has occurred at
several of the north Olympic Peninsula
sites). Other important threats include
changes to the structure and
composition of prairie habitat brought
on by the invasion of shrubs and trees
(Scot’s broom and Douglas-fir) or
nonnative pasture grasses that quickly
invade onto prairies when processes
like fire, or its surrogate mowing, are not
implemented.
These changes to prairie habitat
threaten Taylor’s checkerspot by
degrading prairie habitat and making it
unsuitable for the butterfly. The threats
that lead to habitat degradation and loss
are ubiquitous, occurring rangewide,
and severely affect the survival of the
subspecies, leading to a relatively high
likelihood of extinction. Therefore, the
threats are high in magnitude. The
threats are imminent because they are
ongoing and occur simultaneously at all
of the known locations for the
subspecies. Based on the high
magnitude and the imminent nature of
threats, we retain an LPN of 3 for the
Taylor’s checkerspot butterfly.
Blackline Hawaiian damselfly
(Megalagrion nigrohamatum
nigrolineatum)—We continue to find
that listing this species is warranted but
precluded as of the date of publication
of this notice. However, we are working
on a proposed listing rule that we
expect to publish prior to making the
next annual resubmitted 12-month
petition finding.
Crimson Hawaiian damselfly
(Megalagrion leptodemas)—We
continue to find that listing this species
is warranted but precluded as of the
date of publication of this notice.
However, we are working on a proposed
listing rule that we expect to publish
prior to making the next annual
resubmitted 12-month petition finding.
Oceanic Hawaiian damselfly
(Megalagrion oceanicum)—We continue
to find that listing this species is
warranted but precluded as of the date
of publication of this notice. However,
we are working on a proposed listing
rule that we expect to publish prior to
making the next annual resubmitted
12-month petition finding.
Orangeblack Hawaiian damselfly
(Megalagrion xanthomelas)—The
following summary is based on
information contained in our files. No
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new information was provided in the
petition we received on May 11, 2004.
The Orangeblack Hawaiian damselfly is
a stream-dwelling species endemic to
the Hawaiian Islands of Kauai, Oahu,
Molokai, Maui, Lanai, and Hawaii. The
species no longer is found on Kauai, and
is now restricted to 16 populations on
the islands of Oahu, Maui, Molokai,
Lanai, and Hawaii. This species is
threatened by predation from alien
aquatic species such as fish and
predacious insects, and habitat loss
through dewatering of streams and
invasion by nonnative plants. Nonnative
fish and insects prey on the naiads of
the damselfly, and loss of water reduces
the amount of suitable naiad habitat
available. Invasive plants (e.g.,
California grass (Brachiaria mutica))
also contribute to loss of habitat by
forming dense, monotypic stands that
completely eliminate any open water.
Nonnative fish and plants are found in
all the streams the Orangeblack
damselfly occur in, except the Oahu
location, where there are no nonnative
fish. We assigned this species an LPN of
8 because, although the threats are
ongoing and therefore imminent, they
affect the survival of the species in
varying degrees throughout the range of
the species and are of moderate
magnitude.
Picture-wing fly (Drosophila
digressa)—The following summary is
based on information contained in our
files. No new information was provided
in the petition we received on May 11,
2004, but new information was
provided by one Drosophila expert in
2006. This picture-wing fly, a member
of the family Drosophilidae, feeds only
upon species of Charpentiera, and is
endemic to the Hawaiian Island of
Hawaii. Never abundant in number of
individuals observed, D. digressa was
originally known from 5 population
sites and may now be limited to as few
as 1 or 2 sites. Due to the small
population size of the species and its
small known habitat area, Drosophila
researchers believe this species and its
habitat are particularly vulnerable to a
myriad of threats. Feral ungulates (pigs,
goats, and cattle) degrade and destroy D.
digressa host plants and habitat by
directly trampling plants, facilitating
erosion, and spreading nonnative plant
seeds. Nonnative plants degrade host
plant habitat and compete for light,
space, and nutrients. Direct predation of
D. digressa by nonnative social insects,
particularly yellow jacket wasps, is also
a serious threat. Additionally, this
species faces competition at the larval
stage from nonnative tipulid flies,
which feed within the same portion of
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the decomposing host plant area
normally occupied by the D. digressa
larvae during their development with a
resulting reduction in available host
plant material. Because the threats to
the native forest habitat of D. digressa,
and to individuals of this species, occur
throughout its range and are expected to
continue or increase unless efforts at
control or eradication are undertaken,
they are high in magnitude. In addition,
because of the limited distribution and
small population of the species, any of
the threats would significantly impair
survival of the species. The threats are
also imminent, because they are
ongoing. No known conservation
measures have been taken to date to
specifically address these threats, and
we have therefore assigned this species
an LPN of 2.
Stephan’s riffle beetle (Heterelmis
stephani)—The following summary is
based on information contained in our
files. No new information was provided
in the petition received on May 11,
2004. The Stephan’s riffle beetle is an
endemic riffle beetle found in limited
spring environments within the Santa
Rita Mountains, Pima County, Arizona.
The beetle is known from Sylvester
Spring in Madera Canyon, within the
Coronado National Forest. Threats to
that spring are largely from habitat
modification, from recreational
activities in the springs, and potential
changes in water quality and quantity
due to catastrophic natural events and
climate change. The threats are of low
to moderate magnitude based on our
current knowledge of the permanence of
threats and the likelihood that the
species will persist in areas that are
unaffected by the threats. Although the
threats from climate change are
expected to occur over many years, the
threats from recreational use are
ongoing. Therefore, the threats are
imminent. Thus, we retained an LPN of
8 for the Stephan’s riffle beetle.
Dakota skipper (Hesperia dacotae)—
The following summary is based on
information contained in our files,
including information from the petition
received on May 12, 2003. The Dakota
skipper is a small- to mid-sized butterfly
that inhabits high-quality tallgrass and
mixed-grass prairie in Minnesota, North
Dakota, South Dakota, and the provinces
of Manitoba and Saskatchewan in
Canada. The species is presumed to be
extirpated from Iowa and Illinois and
from many sites within occupied States.
The Dakota skipper is threatened by
degradation of its native prairie habitat
by overgrazing, invasive species, gravel
mining, and herbicide applications;
inbreeding, population isolation, and
prescribed fire threaten some
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populations. Prairie succeeds to
shrubland or forest without periodic
fire, grazing, or mowing; thus, the
species is also threatened at sites where
such disturbances are not applied. The
Service and other Federal agencies,
State agencies, the Sisseton-Wahpeton
Sioux Tribe, and some private
organizations (e.g., The Nature
Conservancy) protect and manage some
Dakota skipper sites. Proper
management is always necessary to
ensure its persistence, even at protected
sites. The species may be secure at a few
sites where public and private
landowners manage native prairie in
ways that conserve Dakota skipper, but
approximately half of the inhabited sites
are privately owned with little or no
protection. A few private sites are
protected from conversion by
easements, but these do not prevent
adverse effects from overgrazing.
Overall, the threats are moderate in
magnitude because they are not
occurring rangewide and have a
moderate effect on the viability of the
species. They are, however, ongoing and
therefore imminent, particularly on
private lands. Thus, we assigned an LPN
of 8 to this species.
Mardon skipper (Polites mardon)—
The following summary is based on
information contained in our files and
the petition we received on December
24, 2002. The Mardon skipper is a
northwestern butterfly with a disjunct
range. Currently this species is known
from four widely separated regions:
South Puget Sound region, southern
Washington Cascades, Siskiyou
Mountains of southern Oregon, and
coastal northwestern California/
southern Oregon. The number of
documented locations for the species
has increased from fewer than 10 in
1997 to more than 130 rangewide in
2010. New site locations have been
documented in each year that targeted
surveys have been conducted since
1999. In the past 9 years, significant
local populations have been located in
the Washington Cascades and in
Southern Oregon, with a few local sites
supporting populations of hundreds of
Mardon skippers.
The Mardon skipper spends its entire
life cycle in one location, often on the
same grassland patch. The dispersal
ability of Mardon skipper is restricted.
The greatest threats currently posed to
Mardon skippers are stochastic events
such as a catastrophic wildfire or
unseasonable weather events. Other
threats to the Mardon skipper include
direct impacts to individuals and local
populations by livestock grazing,
pesticide drift, and off-road-vehicle use.
Habitat destruction or modification
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through conifer encroachment, invasive
nonnative plants, roadside maintenance,
and grassland/meadow management
activities such as prescribed burning
and mowing are also threats. However,
these threats have been substantially
reduced due to protections provided by
State and Federal special status species
programs. The magnitude of the threats
is moderate because current regulatory
mechanisms associated with State and
Federal special status species programs
afford a relatively high level of
protection from additional habitat loss
or destruction across most of the
species’ range. Threats are imminent
because all sites within the species’
range currently have one or more
identified threats that are resulting in
direct impacts to individuals within the
populations, or a gradual loss or
degradation of the species’ habitats.
Mardon skippers face a variety of threats
that may occur at any time at any of the
locations. Low numbers of individuals
have been found at most of the known
locations. Only a few locations are
known to harbor greater than 100
individuals, and specific locations
could easily be lost by changes in
vegetation composition or from the
threat of wildfire. The great distances
between the known locations for the
species would not allow for dispersal of
the species between populations; thus,
loss of any population could lead to
extirpation of the species at any of these
locations. However, the discovery of
new populations and the wide
geographic range for the Mardon skipper
provides a buffer against threats that
could destroy all existing habitat
simultaneously or jeopardize the
continued existence of the species.
Thus, based on imminent threats of
moderate magnitude, we retain an LPN
of 8 to this species.
Coral Pink Sand Dunes tiger beetle
(Cicindela limbata albissima)—The
following summary is based on
information contained in our files,
including information from the petition
we received on April 21, 1994. This
species of beetle occurs only at the Coral
Pink Sand Dunes. This area is
approximately 7 miles west of Kanab,
Kane County, in south-central Utah. It is
restricted to approximately 234 hectares
(577 acres) of protected habitat within
the dune field, situated at an elevation
of about 1,820 meters (6,000 feet).
Continuing drought is negatively
affecting tiger beetle populations.
Drought conditions have suppressed the
beetle’s reproductive capabilities. The
continued survival of the beetle
depends on the preservation of its
habitat and favorable rainfall amounts.
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In addition, the beetle’s habitat is being
adversely affected by ongoing,
recreational off-road-vehicle use that is
limiting expansion of the species. The
two agencies that manage the dune
field, the Utah Department of Parks and
Recreation and the BLM, have restricted
recreational off-road vehicle use in some
areas, which reduces impacts. However,
continued drought may prevent the
population from increasing in size. The
beetle’s population also is vulnerable to
over-collecting by professional and
hobby tiger beetle collectors. We
retained an LPN of 2 due to the high
magnitude and imminence of drought
conditions.
Highlands tiger beetle (Cicindela
highlandensis)—The following
summary is based on information
contained in our files. No new
information was provided in the
petition we received on May 11, 2004.
The Highlands tiger beetle is narrowly
distributed and restricted to areas of
bare sand within scrub and sandhill on
ancient sand dunes of the Lake Wales
Ridge in Polk and Highlands Counties,
Florida. Adult tiger beetles have been
most recently found at 40 sites at the
core of the Lake Wales Ridge. In 2004–
2005 surveys, a total of 1,574 adults
were found at 40 sites, compared with
643 adults at 31 sites in 1996, 928 adults
at 31 sites in 1995, and 742 adults at 21
sites in 1993. Of the 40 sites in the
2004–2005 surveys with one or more
adults, results ranged from 3 sites with
large populations of over 100 adults, to
13 sites with fewer than 10 adults.
Results from a limited removal study at
four sites and similar studies suggest
that the actual population size at some
survey sites can be as much as two
times as high as indicated by the visual
index counts. If assumptions are correct
and unsurveyed habitat is included,
then the total number of adults at all
survey sites might be 3,000 to 4,000.
Habitat loss and fragmentation and
lack of fire and disturbances to create
open habitat conditions are serious
threats; remaining patches of suitable
habitat are disjunct and isolated.
Populations occupy relatively small
patches of habitat and are small and
isolated; individuals have difficulty
dispersing between suitable habitats.
These factors pose serious threats to the
species. Although significant progress in
implementing prescribed fire has
occurred over the last ten years through
collaborative partnerships and the Lake
Wales Ridge Prescribed Fire Team, a
backlog of long-unburned habitat within
conservation areas remains.
Overcollection and pesticide use are
additional concerns. Because this
species is narrowly distributed with
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specific habitat requirements and small
populations, any of the threats could
have a significant impact on the survival
of the species, leading to a relatively
high likelihood of extinction. Therefore,
the magnitude of threats is high.
Although the majority of its historical
range has been lost, degraded, and
fragmented, numerous sites are
protected and land managers are
implementing prescribed fire at some
sites; these actions are expected to
restore habitat and help reduce threats
and have already helped stabilize and
improve the populations. Overall, the
threats are nonimminent. Therefore, we
assigned the Highlands tiger beetle an
LPN of 5.
Arachnids
Warton’s cave meshweaver (Cicurina
wartoni)—The following summary is
based on information contained in our
files. No new information was provided
in the petition received on May 11,
2004. Warton’s Cave meshweaver is an
eyeless, cave-dwelling, unpigmented,
0.23-inch-long invertebrate known only
from female specimens. This
meshweaver is known to occur in only
one cave (Pickle Pit) in Travis County,
Texas. Primary threats to the species
and its habitat are predation and
competition from fire ants, surface and
subsurface effects from runoff from an
adjacent subdivision, unauthorized
entry into the area surrounding the cave,
modification of vegetation near the cave
from human use, and trash dumping
that may include toxic materials near
the feature. The magnitude of threats is
high because the single location for this
species makes it highly vulnerable to
extinction. The threats are imminent
because fire ants are known to occur in
the vicinity of the cave, and impacts to
the cave from runoff and human
activities are an imminent threat. Thus,
we retain an LPN of 2 for this species.
Crustaceans
Anchialine pool shrimp (Metabetaeus
lohena)—The following summary is
based on information contained in our
files. No new information was provided
in the petition we received on May 11,
2004. Metabetaeus lohena is an
anchialine pool-inhabiting species of
shrimp belonging to the family
Alpheidae. This species is endemic to
the Hawaiian Islands and is currently
known from populations on the islands
of Oahu, Maui, and Hawaii. The
primary threats to this species are
predation by fish (which do not
naturally occur in the pools inhabited
by this species) and habitat loss from
degradation (primarily from illegal trash
dumping). The pools where this species
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occurs on the islands of Maui and
Hawaii are located within State Natural
Area Reserves (NAR) and in a National
Park. Both the State NARs and the
National Park prohibit the collection of
the species and the disturbance of the
pools. However, enforcement of
collection and disturbance prohibitions
is difficult, and the negative effects from
the introduction of fish are extensive
and happen quickly. On Oahu, one pool
is located in a National Wildlife Refuge
and is protected from collection and
disturbance to the pool, however, on
State-owned land where the species
occurs, there is no protection from
collection or disturbance of the pools.
Therefore, threats to this species could
have a significant adverse effect on the
survival of the species, leading to a
relatively high likelihood of extinction,
and are of a high magnitude. However,
the primary threats of predation from
fish and loss of habitat due to
degradation are nonimminent overall,
because on the islands of Maui and
Hawaii no fish were observed in any of
the pools where this species occurs and
there has been no documented trash
dumping in these pools. Only one site
on Oahu had a trash dumping instance,
and in that case the trash was cleaned
up immediately and the species
subsequently observed. No additional
dumping events are known to have
occurred. Therefore, we assigned this
species an LPN of 5.
Anchialine pool shrimp
(Palaemonella burnsi)—The following
summary is based on information
contained in our files. No new
information was provided in the
petition we received on May 11, 2004.
Palaemonella burnsi is an anchialine
pool-inhabiting species of shrimp
belonging to the family Palaemonidae.
This species is endemic to the Hawaiian
Islands and is currently known from 3
pools on the island of Maui and 22
pools on the island of Hawaii. The
primary threats to this species are
predation by fish (which do not
naturally occur in the pools inhabited
by this species) and habitat loss due to
degradation (primarily from illegal trash
dumping). The pools where this species
occurs on Maui are located within a
State Natural Area Reserve (NAR).
Hawaii’s State statutes prohibit the
collection of the species and the
disturbance of the pools in State NARs.
On the island of Hawaii, the species
occurs within a State NAR and a
National Park, and collection and
disturbance are also prohibited.
However, enforcement of these
prohibitions is difficult, and the
negative effects from the introduction of
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fish are extensive and happen quickly.
Therefore, threats to this species could
have a significant adverse effect on the
survival of the species, leading to a
relatively high likelihood of extinction,
and are of a high magnitude. However,
the threats are nonimminent, because
surveys in 2004 and 2007 did not find
fish in the pools where these shrimp
occur on Maui or the island of Hawaii.
Also, there was no evidence of recent
habitat degradation at those pools. We
assigned this species an LPN of 5.
Anchialine pool shrimp (Procaris
hawaiana)—The following summary is
based on information contained in our
files. No new information was provided
in the petition we received on May 11,
2004. Procaris hawaiana is an
anchialine pool-inhabiting species of
shrimp belonging to the family
Procarididae. This species is endemic to
the Hawaiian Islands, and is currently
known from two pools on the island of
Maui and thirteen pools on the island of
Hawaii. The primary threats to this
species are predation from fish (which
do not naturally occur in the pools
inhabited by this species) and habitat
loss due to degradation (primarily from
illegal trash dumping). The pools where
this species occurs on Maui are located
within a State Natural Area Reserve
(NAR). Hawaii’s State statutes prohibit
the collection of the species and the
disturbance of the pools in State NARs.
Twelve of the pools on the island of
Hawaii are also located within a State
NAR. However, enforcement of these
prohibitions is difficult and the negative
effects from the introduction of fish are
extensive and happen quickly. In
addition, there are no prohibitions for
either removal of the species or
disturbance to the pool for the one pool
located outside a NAR on the island of
Hawaii. Therefore, threats to this
species could have a significant adverse
effect on the survival of the species,
leading to a relatively high likelihood of
extinction, and thus remain at a high
magnitude. However, the threats to the
species are nonimminent because,
during 2004 and 2007 surveys, no fish
were observed in the pools where these
shrimp occur on Maui, and no fish were
observed in the one pool on the island
of Hawaii during a site visit in 2005. In
addition, there were no signs of trash
dumping or fill in any of the pools
where the species occurs. Therefore, we
assigned this species an LPN of 5.
Anchialine pool shrimp (Vetericaris
chaceorum)—The following summary is
based on information contained in our
files. No new information was provided
in the petition we received on May 11,
2004. Vetericaris chaceorum is an
anchialine pool-inhabiting species of
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shrimp belonging to the family
Procarididae; it is the only species in its
genus. This species is endemic to the
Hawaiian Islands, and is only known
from one population in a single pool on
the island of Hawaii. The primary
threats to this species are predation
from nonnative fish and habitat
degradation (primarily by
contamination from illegal trash
dumping). This species would be highly
vulnerable to predation by any
intentionally or accidentally introduced
fish, or contamination from illegal
dumping into its single known location.
This pool lies within lands
administered by the State of Hawaii
Department of Hawaiian Home Lands.
The threats to V. chaceorum from
habitat degradation and destruction, as
well as from predation by nonnative fish
are of high magnitude, because this
species occurs in only one pool; thus,
the threats could significantly impair
the survival of the species, leading to a
relatively high likelihood of extinction.
All individuals of this species may be
severely affected by a single dumping of
trash or release of nonnative fish in the
species’ only known pool. However, the
threats are nonimminent, as fish have
not been introduced into the pool (nor
is there any reason to believe that
introduction is imminent) and a site
visit in early 2005 showed there were no
signs of dumping or fill. Therefore we
assigned this species an LPN of 4
because the threats are of high
magnitude but nonimminent, and the
species is in a monotypic genus.
Flowering Plants
Abronia alpina (Ramshaw Meadows
sand-verbena)—The following summary
is based on information contained in
our files. No new information was
provided in the petition we received on
May 11, 2004. Abronia alpina is known
from one main population center in
Ramshaw Meadow and a smaller
population in adjacent Templeton
Meadow on the Kern Plateau of the
Sierra Nevada, Inyo National Forest, in
Tulare County, California. The total
estimated area occupied is
approximately 6 hectares (15 acres). The
population fluctuates from year to year
without any clear trends. Population
estimates from 1985–1994 range from a
low of 69,652 plants in 1986 to 132,215
plants in 1987. Surveys conducted since
1994 indicate that no significant
changes have occurred in population
size or location, although, the 2003
survey showed population numbers to
be at the low end of the range. The
population was last monitored in 2009,
and results from those studies are still
being analyzed.
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The factors currently threatening
Abronia alpina include natural and
human habitat alteration, hydrologic
changes to the water table, and
recreational use within meadow
habitats. Lodgepole pine encroachment
has altered the meadow, and trees are
becoming established within A. alpina
habitat. Lodgepole pine encroachment
may alter soil characteristics by
increasing organic matter levels,
decreasing porosity, and moderating
diurnal temperature fluctuations thus
reducing the competitive ability of A.
alpina to persist in an environment
more hospitable to other plant species.
The Ramshaw Meadow ecosystem is
subject to potential alteration by
lowering of the water table due to
downcutting of the South Fork of the
Kern River (SFKR). The SFKR flows
through Ramshaw Meadow, at times
coming within 15 m (50 ft) of A. alpina
habitat, particularly in the vicinity of
five subpopulations. The habitat
occupied by A. alpina directly borders
the meadow system supported by the
SFKR. Drying out of the meadow system
could potentially affect A. alpina
pollinators and/or seed dispersal agents.
Established hiker, packstock, and
cattle trails pass through A. alpina
subpopulations. Two main hiker trails
pass through Ramshaw Meadow, but
were rerouted out of A. alpina
subpopulations where feasible, in 1988
and 1997. Remnants of cattle trails that
pass through subpopulations in several
places receive occasional incidental use
by horses and sometimes hikers. Cattle
use, however, currently is not a threat
due to the 2001 implementation of a 10year moratorium on the Templeton
allotment which prohibits cattle from all
A. alpina locations. The Service is
funding studies to determine
appropriate conservation measures and
working with the U.S. Forest Service on
developing a conservation strategy for
the species. The threats are of a low
magnitude and nonimminent because of
the conservation actions already
implemented. The LPN for A. alpina
remains an 11, with nonimminent
threats of moderate to low magnitude.
Arabis georgiana (Georgia
rockcress)—The following summary is
based on information in our files. No
new information was provided in the
petition we received on May 11, 2004.
The Georgia rockcress grows in a variety
of dry situations, including shallow soil
accumulations on rocky bluffs, ecotones
of gently sloping rock outcrops, and in
sandy loam along eroding river banks. It
is occasionally found in adjacent mesic
woods, but it will not persist in heavily
shaded conditions. Currently, 17
populations are known from the Gulf
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Coastal Plain, Piedmont, and Ridge and
Valley physiographic provinces of
Alabama and Georgia. Populations of
this species typically have a limited
number of individuals over a small area.
Habitat degradation, more than
outright habitat destruction, is the most
serious threat to the continued existence
of this species. Disturbance, associated
with timber harvesting, road building,
and grazing has created favorable
conditions for the invasion of exotic
weeds, especially Japanese honeysuckle
(Lonicera japonica), in this species’
habitat. A large number of the
populations are currently or potentially
threatened by the presence of exotics.
The heritage programs in Alabama and
Georgia have initiated plans for exotic
control at several populations. The
magnitude of threats to this species is
moderate to low due to the number of
populations (17) across multiple
counties in two states and due to the
fact that several sites are protected.
However, since a number of the
populations are currently being affected
by nonnative plants, the threat is
imminent. Thus, we assigned an LPN of
8 to this species.
Argythamnia blodgettii (Blodgett’s
silverbush)—The following summary is
based on information in our files. No
new information was provided in the
petition we received on May 11, 2004.
Blodgett’s silverbush occurs in Florida
and is found in open, sunny areas in
pine rockland, edges of rockland
hammock, edges of coastal berm, and
sometimes in disturbed areas at the
edges of natural areas. Plants can be
found growing from crevices on
limestone, or on sand. The pinerockland habitat where the species
occurs in Miami-Dade County and the
Florida Keys requires periodic fires to
maintain habitat with a minimum
amount of hardwoods. There are
approximately 22 extant occurrences, 12
in Monroe County and 10 in MiamiDade County; many occurrences are on
conservation lands. However, 4 to 5
sites are recently thought to be
extirpated. The estimated population
size of Blodgett’s silverbush in the
Florida Keys, excluding Big Pine Key, is
roughly 11,000; the estimated
population in Miami-Dade County is
375 to 13,650 plants.
Blodgett’s silverbush is threatened by
habitat loss, which is exacerbated by
habitat degradation due to fire
suppression, the difficulty of applying
prescribed fire to pine rocklands, and
threats from exotic plants. Remaining
habitats are fragmented. Threats such as
road maintenance and enhancement,
infrastructure, and illegal dumping
threaten some occurrences. Blodgett’s
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silverbush is vulnerable to natural
disturbances, such as hurricanes,
tropical storms, and storm surges.
Climatic change, particularly sea-level
rise, is a long-term threat that is
expected to continue to affect pine
rocklands and ultimately substantially
reduce the extent of available habitat,
especially in the Keys. Overall, the
magnitude of threats is moderate
because not all of the occurrences are
affected by the threats. In addition, land
managers are aware of the threats from
exotic plants and lack of fire, and are,
to some extent, working to reduce these
threats where possible. While a number
of threats are occurring in some areas,
the threat from development is
nonimminent since most occurrences
are on public land, and sea level rise is
not currently affecting this species.
Overall, the threats are nonimminent.
Thus, we assigned an LPN of 11 to this
species.
Artemisia campestris var.
wormskioldii (Northern wormwood)—
The following summary is based on
information contained in our files. No
new information was provided in the
petition we received on May 11, 2004.
Historically known from eight sites,
northern wormwood is currently known
from two populations in Klickitat and
Grant Counties, Washington. This plant
is restricted to exposed basalt, cobblysandy terraces, and sand habitat along
the shore and on islands in the
Columbia River. The two populations
are separated by 200 miles (322
kilometers) of the Columbia River and
three large hydroelectric dams. The
Klickitat County population is
declining; the status is unclear for the
Grant County population; however, both
are vulnerable to environmental
variability. Surveys have not detected
any additional plants.
Threats to northern wormwood
include direct loss of habitat through
regulation of water levels in the
Columbia River and placement of riprap
along the river bank; human trampling
of plants from recreation; competition
with nonnative invasive species; burial
by wind- and water-borne sediments;
small population sizes; susceptibility to
genetic drift and inbreeding; and the
potential for hybridization with two
other species of Artemisia. Ongoing
conservation actions have reduced
trampling, but have not eliminated or
reduced the other threats at the Grant
County site. Active conservation
measures are not currently in place at
the Klickitat County site. The magnitude
of threat is high for this subspecies
because, although the two remaining
populations are widely separated and
distributed, one or both populations
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could be eliminated by a single
disturbance. The threats are imminent
because recreational use is ongoing,
invasive nonnative species occur at both
sites, erosion of the substrate is ongoing
at the Klickitat County site, and high
water flows are random, naturally
occurring events that may occur
unpredictably in any year. Therefore,
we have retained an LPN of 3 for this
subspecies.
Astragalus anserinus (Goose Creek
milkvetch)—The following summary is
based on information in our files and in
the petition received on February 3,
2004. The majority (over 80 percent) of
Astragalus anserinus sites in Idaho,
Utah, and Nevada occur on Federal
lands managed by the BLM. The rest of
the sites occur as small populations on
private and State lands in Utah and on
private land in Idaho and Nevada. A.
anserinus occurs in a variety of habitats,
but is typically associated with dry
tuffaceous soils from the Salt Lake
Formation. The species grows on steep
or flat sites, with soil textures ranging
from silty to sandy to somewhat
gravelly. The species tolerates some
level of disturbance, based on its
occurrence on steep slopes where
downhill movement of soil is common.
Threats to remaining A. anserinus
individuals include future habitat
degradation and modifications to the
ecosystem in which it occurs because of
an altered wildfire regime.
Approximately 98 percent of the
individual plants that were previously
documented in the areas burned by a
2007 wildfire were killed. Other factors
that may threaten A. anserinus to a
lesser extent include livestock use 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. Threats are high
in magnitude since these threats have
the potential to destroy whole
populations. The threats are
nonimminent since they may occur in
the foreseeable future but not in the near
future. Thus, we have assigned A.
anserinus an LPN of 5.
Astragalus tortipes (Sleeping Ute
milkvetch)—The following summary is
based on information contained in our
files. No new information was provided
in the petition we received on May 11,
2004. Sleeping Ute milkvetch is a
perennial plant that grows only on the
Smokey Hills layer of the Mancos Shale
Formation on the Ute Mountain Ute
Indian Reservation in Montezuma
County, Colorado. In 2000, 3,744 plants
were recorded at 24 locations covering
500 acres within an overall range of
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64,000 acres. Available information
from 2000 indicates that the species
remains stable. Previous and ongoing
threats from borrow pit excavation, offhighway vehicles, irrigation canal
construction, and a prairie dog colony
have had minor impacts that reduced
the range and number of plants by small
amounts. Off-highway-vehicle use of the
habitat has reportedly been controlled
by fencing. Oil and gas development is
active in the general area, but the
Service has received no information to
indicate whether there is development
within plant habitat. The Tribe reported
that the status of the species remains
unchanged, the population is healthy,
and that a management plan for the
species is currently in draft form.
Despite these positive indications, we
have no documentation concerning the
current status of the plants, condition of
habitat, and terms of the species
management plan being drafted by the
Tribe. Thus, at this time, we cannot
accurately assess whether populations
are being adequately protected from
previously existing threats. The threats
are moderate in magnitude, since they
have had minor impacts. Based on
information we have, the population
appears to be stable. Until the
management plan is completed and
made available, there are no regulatory
mechanisms in place to protect the
species. Overall, we conclude threats
are nonimminent. Therefore, we
assigned an LPN of 11 to this species.
Bidens amplectens (Kookoolau)—We
continue to find that listing this species
is warranted but precluded as of the
date of publication of this notice.
However, we are working on a proposed
listing rule that we expect to publish
prior to making the next annual
resubmitted 12-month petition finding.
Bidens campylotheca ssp. pentamera
(Kookoolau)—We continue to find that
listing this species is warranted but
precluded as of the date of publication
of this notice. However, we are working
on a proposed listing rule that we
expect to publish prior to making the
next annual resubmitted 12-month
petition finding.
Bidens campylotheca ssp. waihoiensis
(Kookoolau)—We continue to find that
listing this species is warranted but
precluded as of the date of publication
of this notice. However, we are working
on a proposed listing rule that we
expect to publish prior to making the
next annual resubmitted 12-month
petition finding.
Bidens conjuncta (Kookoolau)—We
continue to find that listing this species
is warranted but precluded as of the
date of publication of this notice.
However, we are working on a proposed
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listing rule that we expect to publish
prior to making the next annual
resubmitted 12-month petition finding.
Bidens micrantha ssp. ctenophylla
(Kookoolau)—The following summary is
based on information contained in our
files. No new information was provided
in the petition we received on May 11,
2004. Bidens micrantha ssp.
ctenophylla is a perennial herb found in
open mixed shrubland to dry
Metrosideros (ohia) forest, and in
recently deposited a‘a lava, on the
island of Hawaii, Hawaii. This
subspecies is known from 4 populations
totaling approximately 360 individuals.
Bidens micrantha ssp. ctenophylla is
threatened by competition with
nonnative plants, and is potentially
threatened by habitat loss due to urban
development and fire. One wild
population of 5 individuals is protected
by an exclosure, and three outplanted
populations are protected by exclosures.
The remaining natural populations are
not protected or managed and are
subject to development. The threats are
high in magnitude because the largest
population of this subspecies is highly
threatened by urban development and
all populations are threatened by fire
and nonnative plants, leading to a
relatively high likelihood of extinction.
Bidens micrantha ssp. ctenophylla is
represented in ex situ collections.
Threats to this subspecies from
competition with nonnative plants are
imminent. Urban development and fire
are potential threats and are nonimminent. Therefore, we retained an
LPN of 3 for this subspecies.
Brickellia mosieri (Florida brickellbush)—The following summary is based
on information contained in our files.
No new information was provided in
the petition we received on May 11,
2004. This species is restricted to pine
rocklands of Miami-Dade County,
Florida. This habitat requires periodic
prescribed fires to maintain the low
understory and prevent encroachment
by native tropical hardwoods and exotic
plants, such as Brazilian pepper. Only
one large occurrence is known to exist;
15 other occurrences contain less than
100 individuals. Eleven occurrences are
on conservation lands, while the rest of
the extant populations are on private
land and are currently vulnerable to
habitat loss and degradation.
Climatic changes and sea-level rise
are long-term threats that will reduce
the extent of habitat. This species is
threatened by habitat loss, which is
exacerbated by habitat degradation due
to fire suppression, the difficulty of
applying prescribed fire to pine
rocklands, and threats from exotic
plants. Remaining habitats are
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fragmented. The species is vulnerable to
natural disturbances, such as
hurricanes, tropical storms, and storm
surges. Due to its restricted range and
the small sizes of most isolated
occurrences, this species is vulnerable
to environmental (catastrophic
hurricanes), demographic (potential
episodes of poor reproduction), and
genetic (potential inbreeding
depression) threats. Ongoing
conservation efforts include projects
aimed at facilitating restoration and
management of public and private lands
in Miami-Dade County and projects to
reintroduce and establish new
populations at suitable sites within the
species’ historical range. The Service is
also pursuing additional habitat
restoration projects, which could help
further improve the status of the
species. Because of these efforts, the
overall magnitude of threats is
moderate. The threats are ongoing and
thus imminent. We assigned this species
an LPN of 8.
Calamagrostis expansa (Maui
reedgrass)—The following summary is
based on information contained in our
files. No new information was provided
in the petition we received on May 11,
2004. Calamagrostis expansa is a
perennial grass found in wet forest and
bogs, and in bog margins, on the islands
of Maui and Hawaii, Hawaii. This
species is known from 13 populations
totaling fewer than 750 individuals.
Calamagrostis expansa is threatened by
habitat degradation and loss by feral
pigs, and by competition with nonnative
plants. Predation by feral pigs is a
potential threat to this species. All of
the known populations of C. expansa on
Maui occur in managed areas. Pig
exclusion fences have been constructed
and control of nonnative plants is
ongoing within the exclosures. On the
island of Hawaii, fencing is planned for
the population in the Upper Waiakea
Forest Reserve. This species is
represented in an ex situ collection.
Threats to this species from feral pigs
and nonnative plants are ongoing, or
imminent, and of high magnitude
because they significantly affect the
species throughout its range, leading to
a relatively high likelihood of
extinction. Predation is a nonimminent
threat. Therefore, we retained an LPN of
2 for this species.
Calamagrostis hillebrandii
(Hillebrand’s reedgrass)—We continue
to find that listing this species is
warranted but precluded as of the date
of publication of this notice. However,
we are working on a proposed listing
rule that we expect to publish prior to
making the next annual resubmitted
12-month petition finding.
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Calochortus persistens (Siskiyou
mariposa lily)—The following summary
is based on information contained in
our files and the petition we received on
September 10, 2001. The Siskiyou
mariposa lily is a narrow endemic that
is restricted to three disjunct ridge tops
in the Klamath-Siskiyou Range on the
California-Oregon border. The
southernmost occurrence of this species
is composed of nine separate sites on
approximately 10 hectares (ha) (24.7
acres (ac)) of Klamath National Forest
and privately owned lands that stretch
for 6 kilometers (km) (3.7 miles (mi))
along the Gunsight-Humbug Ridge,
Siskiyou County, California. In 2007, a
new occurrence was confirmed in the
locality of Cottonwood Peak and Little
Cottonwood Peak, Siskiyou County,
where several populations are
distributed over 164 ha (405 ac) on three
individual mountain peaks in the
Klamath National Forest and on private
lands. The northernmost occurrence
consists of not more than five Siskiyou
mariposa lily plants that were
discovered in 1998, on Bald Mountain,
west of Ashland, Jackson County,
Oregon.
Major threats include competition and
shading by native and nonnative species
fostered by suppression of wild fire;
increased fuel loading and subsequent
risk of wild fire; fragmentation by roads,
fire breaks, tree plantations, and radiotower facilities; maintenance and
construction around radio towers and
telephone relay stations located on
Gunsight Peak and Mahogany Point; and
soil disturbance, direct damage, and
exotic weed and grass species
introduction as a result of heavy
recreational use and construction of fire
breaks. Dyer’s woad (Isatis tinctoria), an
invasive, nonnative plant that may
prevent germination of Siskiyou
mariposa lily seedlings, is now found
throughout the southernmost California
occurrence, affecting 75 percent of the
known lily habitat on Gunsight-Humbug
Ridge. Forest Service staff and the
Klamath-Siskiyou Wildlands Center cite
competition with dyer’s woad as a
significant and chronic threat to the
survival of Siskiyou mariposa lily.
The combination of restricted range,
extremely low numbers (five plants) in
one of three disjunct populations, poor
competitive ability, short seed dispersal
distance, slow growth rates, low seed
production, apparently poor survival
rates in some years, herbivory, habitat
disturbance, and competition from
exotic plants threaten the continued
existence of this species. These threats
are of high magnitude because of their
potential to severely reduce the overall
survival of the species. Because the
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threats of competition from exotic
plants are being addressed, they are not
anticipated to overwhelm a large
portion of the species’ range in the
immediate future, and the threats from
low seed production and survival are
longer-term threats, overall the threats
are nonimminent. Therefore, we
assigned a listing priority number of 5
to this species.
Canavalia pubescens (Awikiwiki)—
The following summary is based on
information contained in our files. No
new information was provided in the
petition we received on May 11, 2004.
Canavalia pubescens is a perennial
climber found in open lava fields and
lowland dryland forest in Hawaii on the
island of Maui, last observed on the
island of Lanai in 1998, and was last
observed on the island of Niihau in
1949. This species is known from 5
populations totaling 360 to 500
individuals. Canavalia pubescens is
threatened by development (Maui),
goats (Maui) and axis deer (Maui and
Lanai) that degrade and destroy habitat,
and by nonnative plants that
outcompete and displace native plants
(both islands). Fire is a possible threat
at the Keokea population on Maui.
Ungulate exclosure fences protect 6
individuals of C. pubescens at Papaka
Kai and 20 to 30 individuals at AhihiKinau NAR, and weed control is
ongoing at these locations on Maui. This
species is represented in ex situ
collections. Threats to this species from
feral goats, axis deer, and nonnative
plants are ongoing, or imminent, and of
high magnitude because they severely
affect the species throughout its range,
leading to a relatively high likelihood of
extinction. Fire is a nonimminent threat.
Therefore, we retained an LPN of 2 for
this species.
Castilleja christii (Christ’s
paintbrush)—The following summary is
based on information contained in our
files and the petition we received on
January 2, 2001. Castilleja christii is
found in one population covering
approximately 85 ha (220 ac) on the
summit of Mount Harrison in Cassia
County, Idaho. This endemic species is
considered a hemiparasite (dependent
on the health of their surrounding
native plant community), and it grows
in association with subalpine-meadow
and sagebrush habitats. The population
may be large (greater than 10,000
individual plants); however, the species
is considered to be subject to large
variations in annual abundance and an
accurate current population estimate is
not available. Monitoring indicates that
reproductive stems per plant and plant
density declined between 1995 and
2007. Fluctuations have occurred since
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2007, with slight increases in
reproductive output and density in 2008
and decreases in 2009.
The primary threat to the species is
the nonnative invasive plant smooth
brome (Bromus inermis). Despite
cooperative Forest Service and Service
efforts to control smooth brome in 2007,
2008, and 2009, it still persists in C.
christii habitats. Other threats to C.
christii from recreational use and
livestock trespass appear to be mostly
seasonal and affect only a small portion
of the population, and may not occur
every year. The magnitude of the threats
to this species is moderate at this time
because, although the smooth brome
control efforts have not eliminated the
invasive plant, the Service and Forest
Service are continuing their efforts in
order to conserve this species. The
threat from smooth brome is imminent
because the threat still persists at a level
that affects the native plant
communities that provide habitat for C.
christii. Thus, we assign an LPN of 8 to
this species.
Chamaecrista lineata var. keyensis
(Big Pine partridge pea)—The following
summary is based on information
contained in our files. No new
information was provided in the
petition we received on May 11, 2004.
This pea is endemic to the lower Florida
Keys, and restricted to pine rocklands,
hardwood hammock edges, and
roadsides and firebreaks within these
ecosystems. Historically, it was known
from Big Pine, Cudjoe, No Name,
Ramrod, and Little Pine Keys (Monroe
County, Florida). In 2005, a small
population was detected on lower
Sugarloaf Key, but this population was
apparently extirpated later in 2005, due
to the effects of Hurricane Wilma. It
presently occurs on Big Pine Key, with
a very small population on Cudjoe Key.
It is fairly well distributed in Big Pine
Key pine rocklands, which encompass
approximately 580 hectares (1,433
acres), approximately 360 hectares (890
acres) of which are within the Service’s
National Key Deer Refuge (NKDR). Over
80 percent of the population probably
exists on NKDR, with the remainder
distributed among State, County, and
private properties. Hurricane Wilma
(October 2005) resulted in a storm surge
that covered most of Big Pine Key with
sea water. The surge reduced the
population by as much as 95 percent in
some areas.
Pine rockland communities are
maintained by relatively frequent fires.
In the absence of fire, shrubs and trees
encroach on pine rockland and this
subspecies is eventually shaded out.
NKDR has a prescribed fire program,
although with many constraints on
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implementation. Habitat loss due to
development was historically the
greatest threat to the pea. Much of the
remaining habitat is now protected on
public lands. Absence of fire now
appears to be the greatest of the
deterministic threats. Given the recent
increase in hurricane activity, storm
surges are the greatest of the stochastic
threats. The small range and patchy
distribution of the subspecies increase
risk from stochastic events. Climatic
changes and sea level rise are serious
long-term threats. Models indicate that
even under the best of circumstances, a
significant proportion of upland habitat
will be lost on Big Pine Key by 2100.
Additional threats include restricted
range, invasive exotic plants, roadside
dumping, loss of pollinators, seed
predators, and development.
We maintain the previous assessment
that hurricane storm surges, lack of fire,
and limited distribution results in a
moderate magnitude of threat because a
large part of the range is on conservation
lands wherein threats are being
controlled, although fire management is
at much slower rate than is required.
The immediacy of hurricane threats is
difficult to characterize, but imminence
is considered high given that hurricanes
(and storm surges) of various
magnitudes are frequent and recurrent
events in the area. Sea-level rise remains
uncontrolled, but overall, is
nonimminent. Overall, the threats from
limited distribution and inadequate fire
management are imminent since they
are ongoing. In addition, the most
consequential threats (hurricanes, storm
surges) are frequent, recurrent, and
imminent. Therefore, we retained an
LPN of 9 for Big Pine partridge pea.
Chamaesyce deltoidea ssp. pinetorum
(Pineland sandmat)—The following
summary is based on information
contained in our files. No new
information was provided in the
petition we received on May 11, 2004.
The pineland sandmat in only known
from Miami-Dade County, Florida. The
largest occurrence, estimated at more
than 10,000 plants, is located on Long
Pine Key within Everglades National
Park. All other occurrences are smaller
and are in isolated pine rockland
fragments in heavily urbanized MiamiDade County.
Occurrences on private (nonconservation) lands and on one Countyowned parcel are at risk from
development and habitat degradation
and fragmentation. Conditions related to
climate change, particularly sea-level
rise, will be a factor over the long term.
All occurrences of the species are
threatened by habitat loss and
degradation due to fire suppression, the
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difficulty of applying prescribed fire,
and exotic plants. These threats are
severe within small and unmanaged
fragments in urban areas. However, the
threats of fire suppression and exotics
are reduced on lands managed by the
National Park Service. Hydrologic
changes are considered to be another
threat. Hydrology has been altered
within Long Pine Key due to artificial
drainage, which lowered ground water,
and by the construction of roads, which
either impounded or diverted water.
Regional water management intended to
restore the Everglades could negatively
affect the pinelands of Long Pine Key in
the future. At this time, we do not know
whether the proposed restoration and
associated hydrological modifications
will have a positive or negative effect on
pineland sandmat. This narrow endemic
may be vulnerable to catastrophic
events and natural disturbances, such as
hurricanes. Overall, the magnitude of
threats to this species is moderate; by
applying regular prescribed fire, the
National Park Service has kept Long
Pine Key’s pineland vegetation intact
and relatively free of exotic plants, and
partnerships are in place to help address
the continuing threat of exotics on other
pine rockland fragments. Overall, the
threats are non-imminent since fire
management at the largest occurrence is
regularly conducted and sea-level rise
and hurricanes are longer-term threats.
Therefore, we assigned an LPN of 12 to
this subspecies.
Chamaesyce deltoidea ssp. serpyllum
(Wedge spurge)—The following
summary is based on information
contained in our files. No new
information was provided in the
petition we received on May 11, 2004.
Systematic surveys of publicly owned
pine rockland throughout this plant’s
range were conducted during 2005–
2006 and 2007–2008 to determine
population size and distribution. Wedge
spurge is a small prostrate herb. It was
historically, and remains, restricted to
pine rocklands on Big Pine Key in
Monroe County, Florida. Pine rocklands
encompass approximately 580 hectares
(1,433 acres) on Big Pine Key,
approximately 360 hectares (890 acres)
of which are within the Service’s
National Key Deer Refuge (NKDR). Most
of the species’ range falls within the
NKDR, with the remainder on State,
County, and private properties. It is not
widely dispersed within the limited
range. Occurrences are sparser in the
southern portion of Big Pine Key, which
contains smaller areas of NKDR lands
than does the northern portion. Wedge
spurge inhabits sites with low woody
cover (e.g., low palm and hardwood
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densities) and usually, exposed rock or
gravel.
Pine rockland communities are
maintained by relatively frequent fires.
In the absence of fire, shrubs and trees
encroach on pine rockland and the
subspecies is eventually shaded out.
NKDR has a prescribed fire program,
although with many constraints on
implementation. Habitat loss due to
development was historically the
greatest threat to the wedge spurge.
Much of the remaining habitat is now
protected on public lands. Absence of
fire now appears to be the greatest of the
deterministic threats. Given the recent
increase in hurricane activity, storm
surges are the greatest of the stochastic
threats. The small range and patchy
distribution of the subspecies increases
risk from stochastic events. Climatic
changes and sea-level rise are serious
long-term threats. Models indicate that
even under the best of circumstances, a
significant proportion of upland habitat
will be lost on Big Pine Key by 2100.
Additional threats include restricted
range, invasive exotic plants, roadside
dumping, loss of pollinators, seed
predators, and development.
We maintain the previous assessment
that low fire return intervals plus
hurricane-related storm surges, in
combination with a limited, fragmented
distribution and threats from sea level
rise, result in a moderate magnitude of
threat, in part, because a large part of
the range is on conservation lands,
where some threats can be substantially
controlled. The immediacy of hurricane
threats is difficult to categorize, but in
this case threats are imminent given that
hurricanes (and storm surges) of various
magnitudes are frequent and recurrent
events in the area. Sea level rise remains
uncontrolled, but over much of the
range is nonimminent compared to
other prominent threats. Threats
resulting from limited fire occurrences
are imminent. Since major threats are
ongoing, overall, the threats are
imminent. Therefore, we retained an
LPN of 9 for this subspecies.
Chorizanthe parryi var. fernandina
(San Fernando Valley spineflower)—
The following summary is based on
information contained in our files and
the petition we received on December
14, 1999. Chorizanthe parryi var.
fernandina is a low-growing herbaceous
annual plant in the buckwheat family.
Germination occurs following the onset
of late-fall and winter rains and
typically represents different cohorts
from the seed bank. Flowering occurs in
the spring, generally between April and
June. The plant currently is known from
two disjunct localities: The first is in the
southeastern portion of Ventura County
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on a site within the Upper Las Virgenes
Canyon Open Space Preserve, formerly
known as Ahmanson Ranch, and the
second is in an area of southwestern Los
Angeles County known as Newhall
Ranch. Investigations of historical
locations and seemingly suitable habitat
within the range of the species have not
revealed any other occurrences.
The threats currently facing
Chorizanthe parryi var. fernandina
include threatened destruction,
modification, or curtailment of its
habitat or range, and other natural or
manmade factors. The threats to
Chorizanthe parryi var. fernandina from
habitat destruction or modification are
slightly less than they were 6 years ago.
One of the two populations (Upper Las
Virgenes Canyon Open Space Preserve)
is in permanent, public ownership and
is being managed by an agency that is
working to conserve the plant; however,
the use of adjacent habitat for filming
movies was brought to our attention last
year; while we are monitoring the
situation, we have not yet completed
our evaluation of the potential impacts
to Chorizanthe parryi var. fernandina.
We will be working with the
landowners to manage the site for the
benefit of Chorizanthe parryi var.
fernandina. The other population
(Newhall Ranch) is under the threat of
development; however, a Candidate
Conservation Agreement (CCA) is being
developed with the landowner, and it is
possible that the remaining plants can
also be conserved. Until such an
agreement is finalized, the threat of
development and the potential damage
to the Newhall Ranch population still
exists, as shown by the destruction of
some plants during installation of an
agave farm. Furthermore, cattle grazing
on Newhall Ranch may be current
threat. Cattle grazing may harm
Chorizanthe parryi var. fernandina by
trampling and soil compaction. Grazing
activity could also alter the nutrient
content of the soils Chorizanthe parryi
var. fernandina habitat through fecal
inputs, which in turn may favor the
growth of other plant species that would
otherwise not grow so readily on the
mineral-based soils. Over time, changes
in species composition may render the
sites less favorable for the persistence of
Chorizanthe parryi var. fernandina.
Chorizanthe parryi var. fernandina may
be threatened by invasive nonnative
plants, including grasses, which could
potentially displace it from available
habitat; compete for light, water, and
nutrients; and reduce survival and
establishment.
Chorizanthe parryi var. fernandina is
particularly vulnerable to extinction due
to its concentration in two isolated
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areas. The existence of only two areas of
occurrence, and a relatively small range,
makes the variety highly susceptible to
extinction or extirpation from a
significant portion of its range due to
random events such as fire, drought,
erosion, or other occurrences. We
retained a listing priority number of 6
for Chorizanthe parryi var. fernandina
due to high magnitude of nonimminent
threats.
Chromolaena frustrata (Cape Sable
thoroughwort)—The following summary
is based on information contained in
our files. No new information was
provided in the petition we received on
May 11, 2004. This species is found
most commonly in open sun to partial
shade at the edges of rockland tropical
hammock and in coastal rock barrens.
There are nine extant occurrences
located on five islands in the Florida
Keys and one small area in Everglades
National Park (ENP). In the Keys, the
plant has been extirpated from half of
the islands where it occurred. Prior to
Hurricane Wilma in 2005, the
population was estimated at roughly
5,000 individuals, with all but 500
occurring on one privately owned
island. An estimated 1,500 plants occur
on the mainland within ENP.
This species is threatened by habitat
loss and modification, even on public
lands, and habitat loss and degradation
due to threats from exotic plants at
almost all sites. The species is
vulnerable to natural disturbances, such
as hurricanes, tropical storms, and
storm surges. While these factors may
also work to maintain coastal rock
barren habitat in the long term,
Hurricane Wilma affected occurrences
and habitat, at least in the short term.
Occurrences probably initially declined
due to inundation of its coastal barren
and rockland hammock habitats; longterm effects on this species are
unknown. Cape Sable thoroughwort
appears to be vulnerable to cold
temperatures. It is not known to what
extent cold temperatures in January
2010 may have affected the species at
most locations, or what, if any, longterm effect this may have on the
population. Sea level rise is considered
a major threat over the long term.
Potential effects from other changes in
freshwater deliveries and the
construction of the Buttonwood Canal
are unknown. Problems associated with
small population size and isolation are
likely major factors, as occurrences may
not be large enough to be viable; this
narrowly endemic plant has uncertain
viability at most locations. Thus, these
factors constitute a high magnitude of
threat. The threats of small population
size, isolation, and uncertain viability
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are imminent because they are ongoing.
As a result, we assigned an LPN of 2 to
this species.
Consolea corallicola (Florida
semaphore cactus)—The following
summary is based on information in our
files. No new information was provided
in the petition we received on May 11,
2004. The Florida semaphore cactus is
endemic to the Florida Keys, and was
discovered on Big Pine Key in 1919, but
that population was extirpated as a
result of road building and poaching.
This cactus grows close to salt water on
bare rock with a minimum of humus
soil cover in or along the edges of
hammocks near sea level. The species is
known to occur naturally only in two
areas, Swan Key within Biscayne
National Park and Little Torch Key.
Outplantings have been attempted in
several locations in the upper and lower
Keys; however, success has been low.
Few plants remain in the population at
The Nature Conservancy’s Torchwood
Hammock Preserve on Little Torch Key.
During monitoring work conducted in
2005, a total of 655 plants were
documented at the Swan Key
population. In 2008 and 2009 the
population was estimated by Biscayne
National Park staff to consist of
approximately 600 individuals. Asexual
reproduction is the main life history
strategy of this species. Recent genetic
studies have shown no variation within
populations and very limited variation
between populations. Findings support
the conclusion that the Swan Key
(upper Keys) and Little Torch Key
(lower Keys) populations and an
individual plant from Big Pine Key
(single plant in ex situ collection; lower
Keys) are clonally derived. Studies
examining the reproductive biology of
the species indicate that all extant wild
and cultivated plants are male.
The causes for the population decline
of this species include destruction or
modification of habitat, predation from
nonnative Cactoblastis cactorum moths
and disease, poaching and vandalism,
sea level rise, and hurricanes. Sea level
rise is considered a serious threat to the
species and its habitat; all extant
populations are located in low-lying
areas. All remaining populations are
under threat of predation from the
exotic moth and are susceptible to rootrot disease. Competition from invasive
exotic plants is a threat at Swan Key;
however, efforts by Biscayne National
Park are underway to address this
threat. This species is inherently
vulnerable to stochastic losses,
especially at its smaller populations. A
lack of variation and limited sexual
reproduction makes the remaining small
population even more susceptible to
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natural or manmade factors. Overall, the
magnitude of threats is high. The
numerous threats are ongoing and
therefore, are imminent. Thus, we
assigned this species an LPN of 2.
Cordia rupicola (no common name)—
The following summary is based on
information contained in our files. No
new information was provided in the
petition we received on May 11, 2004.
Cordia rupicola, a small shrub, has been
described from southwestern Puerto
Rico, Vieques Island, and Anegada
Island (British Virgin Islands). All sites
lay within the subtropical dry forest life
zone overlying a limestone substrate.
Cordia rupicola has a restricted
distribution. Currently, approximately
226 individuals are known from 3
˜
locations in Puerto Rico: Penuelas and
´
Guanica Commonwealth Forests and
Vieques National Wildlife Refuge. The
species is reported as common in
Anegada.
This species is threatened by
maintenance of trails and power line
´
right-of-ways in the Guanica
Commonwealth Forest, residential
˜
development in Penuelas, and
residential and commercial
development in Anegada Island. This
species is also vulnerable to natural
(e.g., hurricanes) or manmade (e.g.,
human-induced fires) threats.
Approximately 68 percent of the
currently known reproductive adults are
´
located in the Guanica Commonwealth
Forest where, due to the difficulty in
identifying this species, it is threatened
by management and maintenance
activities; another 32 percent of the
currently known reproductive adults in
Puerto Rico are located on privately
owned property currently threatened by
habitat destruction or modification. For
these reasons, we conclude that the
magnitude of the current threats is high.
The threats this species faces are ones
that are likely to increase in the future
if conservation measures are not
implemented and long-term impacts are
not averted. For these reasons, we
conclude threats to the species as a
whole are nonimminent, and therefore
have assigned an LPN of 5.
Cyanea asplenifolia (Haha)—We
continue to find that listing this species
is warranted but precluded as of the
date of publication of this notice.
However, we are working on a proposed
listing rule that we expect to publish
prior to making the next annual
resubmitted 12-month petition finding.
Cyanea calycina (Haha)—We
continue to find that listing this species
is warranted but precluded as of the
date of publication of this notice.
However, we are working on a proposed
listing rule that we expect to publish
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prior to making the next annual
resubmitted petition 12-month finding.
Cyanea kunthiana (Haha)—We
continue to find that listing this species
is warranted but precluded as of the
date of publication of this notice.
However, we are working on a proposed
listing rule that we expect to publish
prior to making the next annual
resubmitted 12-month petition finding.
Cyanea lanceolata (Haha)—We
continue to find that listing this species
is warranted but precluded as of the
date of publication of this notice.
However, we are working on a proposed
listing rule that we expect to publish
prior to making the next annual
resubmitted 12-month petition finding.
Cyanea obtusa (Haha)—We continue
to find that listing this species is
warranted but precluded as of the date
of publication of this notice. However,
we are working on a proposed listing
rule that we expect to publish prior to
making the next annual resubmitted 12month petition finding.
Cyanea tritomantha (’Aku)—The
following summary is based on
information contained in our files. No
new information was provided in the
petition we received on May 11, 2004.
Cyanea tritomantha is a palm-like tree
found in Metrosideros-Cibotium (ohiahapuu) montane wet forest on the island
of Hawaii, Hawaii. This species is
known from 16 populations totaling
fewer than 300 individuals. Cyanea
tritomantha is threatened by feral pigs
and cattle that degrade and destroy
habitat, and nonnative plants that
outcompete and displace it. Potential
threats to this species include predation
by feral pigs, cattle, rats, and slugs, and
human trampling of plants located near
trails. Feral pigs and cattle have been
fenced out of three outplanted
populations of C. tritomantha, and
nonnative plants have been reduced in
the fenced areas; however, there are no
efforts to control the ongoing and
imminent threats to the remaining
populations. The threats continue to be
of a high magnitude to C. tritomantha
because they significantly affect the
species resulting in direct mortality or
reduced reproductive capacity, leading
to a relatively high likelihood of
extinction. They are ongoing and
therefore imminent for more than 75
percent of the population where no
control measures have been
implemented. Because the threats
continue to be of a high magnitude and
are imminent for the unmanaged
populations, we retained an LPN of 2 for
this species.
Cyrtandra filipes (Haiwale)—We
continue to find that listing this species
is warranted but precluded as of the
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date of publication of this notice.
However, we are working on a proposed
listing rule that we expect to publish
prior to making the next annual
resubmitted 12-month petition finding.
Cyrtandra kaulantha (Haiwale)—We
continue to find that listing this species
is warranted but precluded as of the
date of publication of this notice.
However, we are working on a proposed
listing rule that we expect to publish
prior to making the next annual
resubmitted 12-month petition finding.
Cyrtandra oxybapha (Haiwale)—We
continue to find that listing this species
is warranted but precluded as of the
date of publication of this notice.
However, we are working on a proposed
listing rule that we expect to publish
prior to making the next annual
resubmitted 12-month petition finding.
Cyrtandra sessilis (Haiwale)—We
continue to find that listing this species
is warranted but precluded as of the
date of publication of this notice.
However, we are working on a proposed
listing rule that we expect to publish
prior to making the next annual
resubmitted 12-month petition finding.
Dalea carthagenensis ssp. floridana
(Florida prairie-clover)—The following
summary is based on information
contained in our files. No new
information was provided in the
petition we received on May 11, 2004.
Dalea carthagenensis var. floridana
occurs in Big Cypress National Preserve
(BCNP) in Monroe and Collier Counties
and at six locations within Miami-Dade
County, Florida, albeit mostly in limited
numbers. There are a total of nine extant
occurrences, seven of which are on
conservation lands.
Existing occurrences are extremely
small and may not be viable, especially
some of the occurrences in Miami-Dade
County. Remaining habitats are
fragmented. Climatic changes and sealevel rise are long-term threats that are
expected to reduce the extent of habitat.
This plant is threatened by habitat loss
and degradation due to fire suppression,
the difficulty of applying prescribed fire
to pine rocklands, and threats from
exotic plants. Damage to plants by offroad vehicles is a serious threat within
the BCNP; damage attributed to illegal
mountain biking at the R. Hardy
Matheson Preserve has been reduced.
One location within BCNP is threatened
by changes in mowing practices; this
threat is low in magnitude. This species
is being parasitized by the introduced
insect lobate lac scale (Paratachardina
pseudolobata) at some localities (e.g., R.
Hardy Matheson Preserve), but we do
not know the extent of this threat. This
plant is vulnerable to natural
disturbances, such as hurricanes,
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tropical storms, and storm surges. Due
to its restricted range and the small sizes
of most isolated occurrences, this
species is vulnerable to environmental
(catastrophic hurricanes), demographic
(potential episodes of poor
reproduction), and genetic (potential
inbreeding depression) threats. The
magnitude of threats is high because of
the limited number of occurrences and
the small number of individual plants at
each occurrence. The threats are
imminent; even though many sites are
on conservation lands, these plants still
face significant ongoing threats.
Therefore, we have assigned an LPN of
3 to this subspecies.
Dichanthelium hirstii (Hirsts’ panic
grass)—The following summary is based
on information contained in our files.
No new information was provided in
the petition we received on May 11,
2004. Dichanthelium hirstii is a
perennial grass that produces erect leafy
flowering stems from May to October.
Dichanthelium hirstii occurs in coastal
plain intermittent ponds, usually in wet
savanna or pine barren habitats and is
found at only two sites in New Jersey,
one site in Delaware, and one site in
North Carolina. While all four extant D.
hirstii populations are located on public
land or privately owned conservation
lands, natural threats to the species from
encroaching vegetation and fluctuations
in climatic conditions remain of
concern and may be exacerbated by
anthropomorphic factors occurring
adjacent to the species’ wetland habitat.
Given the low numbers of plants found
at each site, even minor changes in the
species’ habitat could result in local
extirpation. Loss of any known sites
could result in a serious contraction of
the species’ range. However, the most
immediate and severe of the threats to
this species (i.e., ditching of the
Labounsky Pond site, and encroachment
of aggressive vegetative competitors)
have been curtailed or are being actively
managed by The Nature Conservancy at
one New Jersey site and by the Delaware
Division of Fish and Wildlife and
Delaware Natural Heritage Program at
the Assawoman Pond, Delaware site.
Based on nonimminent threats of a high
magnitude, we retain an LPN of 5 for
this species.
Digitaria pauciflora (Florida pineland
crabgrass)—The following summary is
based on information contained in our
files. No new information was provided
in the petition we received on May 11,
2004. Pine rocklands in Miami-Dade
County have largely been destroyed by
residential, commercial, and urban
development and agriculture. With most
remaining habitat having been
negatively altered, this species has been
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extirpated from much of its historical
range, including extirpation from all
areas outside of National Parks. Two
large occurrences remain within
Everglades National Park and Big
Cypress National Preserve; plants on
Federal lands are protected from the
threat of habitat loss due to
development. However, any unknown
plants, indefinite occurrences, and
suitable habitat remaining on private or
non-conservation land are threatened by
development. Continued development
of suitable habitat diminishes the
potential for reintroduction into its
historical range. Extant occurrences are
in low-lying areas and will be affected
by climate change and rising sea level.
Fire suppression, the difficulty of
applying prescribed fire to pine
rocklands, and threats from exotic
plants are ongoing threats. Since the
only known remaining occurrences are
on lands managed by the National Park
Service, the threats of fire suppression
and exotics are somewhat reduced. The
presence of the exotic Old World
climbing fern is of particular concern
due to its ability to spread rapidly. In
Big Cypress National Preserve, plants
are threatened by off-road-vehicle use.
Changes to hydrology are a potential
threat. Hydrology has been altered
within Long Pine Key due to artificial
drainage, which lowered ground water,
and construction of roads, which either
impounded or diverted water. Regional
water management intended to restore
the Everglades has the potential to affect
the pinelands of Long Pine Key, where
a large population occurs. At this time,
it is not known whether Everglades
restoration will have a positive or
negative effect. This narrow endemic
may be vulnerable to catastrophic
events and natural disturbances, such as
hurricanes. Overall, the magnitude of
threats is high. Only two known
occurrences remain and the likelihood
of establishing a sizable population on
other lands is diminished due to
continuing habitat loss. Impacts from
climate change and sea level rise are
currently low, but expected to be severe
in the future. The majority of threats are
nonimminent as they are long-term in
nature (water management, hurricanes,
and sea-level rise). Therefore, we
assigned an LPN of 5 for this species.
Echinomastus erectocentrus var.
acunensis (Acuna cactus)—The
following summary is based on
information contained in our files and
the petition we received on October 30,
2002. The Acuna cactus is known from
six sites on well-drained gravel ridges
and knolls on granite soils in Sonoran
Desert scrub association at 1,300 to
2,000 feet in elevation. Habitat
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destruction has been a threat in the past
and is a potential future threat to this
species. New roads and illegal activities
have not yet directly affected the cactus
populations at Organ Pipe Cactus
National Monument, but areas in close
proximity to these known populations
have been altered. Cactus populations
located in the Florence area have not
been monitored and these populations
may be in danger of habitat loss due to
recent urban growth in the area. Urban
development near Ajo, Arizona, as well
as that near Sonoyta, Mexico, is a
significant threat to the Acuna cactus.
Populations of the Acuna cactus within
the Organ Pipe Cactus National
Monument have shown a 50-percent
mortality rate in recent years. The
reason(s) for the mortality are not
known, but continuing drought
conditions are thought to play a role.
The Arizona Plant Law and the
Convention on International Trade in
Endangered Species of Wild Fauna and
Flora provide some protection for the
Acuna cactus. However, illegal
collection is a primary threat to this
cactus variety and has been documented
on the Organ Pipe Cactus National
Monument in the past. The threats
continue to be of a high magnitude
because drought, as the main threat,
severely affects the long-term viability
of this variety. The threats are
imminent, mainly due to the continued
decline of the species, most likely from
effects from the ongoing drought.
Conditions in 2006 to 2008 worsened,
and the drought is prevalent throughout
the range of this variety. Therefore, we
assigned an LPN of 3 to this cactus
variety.
Erigeron lemmonii (Lemmon
fleabane)—The following summary is
based on information contained in our
files and the petition we received in July
1975. The species is known from one
site in a canyon in the Fort Huachuca
Military Reservation (Fort Huachuca) of
southeastern Arizona. In the 1990s,
surveys found approximately 450
plants. A survey in 2006 found
approximately 950 plants; occupied
habitat encompasses about 1 square
kilometer. The threats to this species are
from catastrophic wildfire in the canyon
and on-going drought conditions. We do
not know if this species has any
adaptations to fire. Due to its location
on cliffs, we suspect that fires that may
have occurred at more regular intervals
and burned at low intensities may have
had little to no effect on this species.
Lack of fire and the accumulated fuel
load that lead to high fire intensity and
associated heat may now damage or kill
plants on adjacent cliffs, especially near
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the ground. Plants that are much higher
on the cliff face would probably not be
affected. The magnitude of threats is
moderate rather than high because it is
likely that not all of the population
would be adversely affected by a
wildfire or drought. The threats are still
imminent because the likelihood of a
fire is high. The LPN for Lemmon
fleabane remains an 8 due to moderate,
imminent threats.
Eriogonum codium (Umtanum Desert
buckwheat)—The following summary is
based on information contained in our
files. No new information was provided
in the petition we received on May 11,
2004. This species is a long-lived, slowgrowing, woody perennial plant that
forms low dense mats. The species
occupies a single location on the
Hanford National Monument in
Washington State. It is found only on an
exposed basalt ridge; we do not know if
this association is related to the
chemical or physical characteristics of
the bedrock or other factors. Individual
plants may exceed 100 years of age,
based on counts of annual growth rings.
A count in 1997 reported 5,228
individuals; by 2005 the figure had
dropped to 4,418, declining 15 percent
over 8 years. In the summer of 2011,
another full population census will
likely be undertaken, providing a useful
measure of change over the last 14
years.
A population viability analysis in
2006 based on 9 years of demographic
data estimated that that there is a 72
percent chance of a decline of 50
percent within the next 100 years.
Another analysis is expected in 2010,
based on 12 years of demographic
monitoring.
The major threats to the species are
wildfire, firefighting activities,
trampling, and invasive weeds.
However, the relationship between the
decline in population numbers and the
known threats is not understood at this
time. With the possible exception of
wildfire, the observed decline in
population numbers and recruitment
since 1997 is not directly attributable to
the currently known threats. Because
the population is small, limited to a
single site, and sensitive to fire and
disturbance, the species remains
vulnerable to the identified threats. The
magnitude of threats is high because,
given the limited range of the species,
any of the threats could adversely affect
its continued existence. The threats are
ongoing and, therefore, imminent.
Because the species continues to remain
vulnerable to these threats, we retained
an LPN of 2 for this species.
Eriogonum corymbosum var. nilesii
(Las Vegas buckwheat)—The following
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summary is based on information
contained in our files and the petition
we received on April 23, 2008.
Eriogonum corymbosum var. nilesii is a
woody perennial shrub up to 4 feet high
with a mounding shape. The flowers of
this plant are numerous, small, and
yellow with small bract-like leaves at
the base of each flower. Eriogonum
corymbosum var. nilesii is very
conspicuous when flowering in late
September and early October. It is
restricted to gypsum soil outcroppings
in Clark County, Nevada. In 2004,
morphometrics (the study of variation
and change in the form (size and shape)
of organisms) were used to classify this
plant as the unique variety nilesii, and
its unique taxonomy was verified using
molecular genetic analyses in 2007.
Eriogonum corymbosum var. nilesii
was added to the candidate list in
December 2007 due to continued loss of
habitat from development of over 95
percent of its core historical range and
potential habitat. In addition, offhighway vehicle activity and other
public-land uses (casual public use,
mining, and illegal dumping) directly
threaten over 95 percent of the
remaining habitat. It was petitioned for
listing in April 2008 and a warrantedbut-precluded determination was made
in December 2008. To date, regulatory
mechanisms to protect E. corymbosum
var. nilesii are inadequate. Its
designation as a Bureau of Land
Management (BLM) special status
species has not provided adequate
protection on lands managed by BLM.
Eriogonum corymbosum var. nilesii is
not protected by the State of Nevada or
any other regulatory mechanisms on
other Federal lands. We have
determined that candidate status is
warranted for this variety as a result of
threats to the remaining habitat and
inadequate regulatory mechanisms.
Conservation measures are being
developed that could reduce the risks to
occupied habitat, but these measures are
not sufficiently complete as to remove
these threats. The magnitude of threats
is high since the more significant threats
(urban development and surface
mining) would result in direct mortality
of the plants in over half of the known
habitat. While both development and
mining are very likely to occur in the
future, they are not expected to happen
in the immediate future, and thus, the
threats are nonimminent. Accordingly,
we assigned E. corymbosum var. nilesii
an LPN of 6.
Eriogonum kelloggii (Red Mountain
buckwheat)—The following summary is
based on information contained in our
files and information provided by the
California Department of Fish and
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Game. No new information was
provided in the petition we received on
May 11, 2004. Red Mountain buckwheat
is a perennial herb endemic to
serpentine habitat of lower montane
forests found between 1,900 and 4,100
feet. Its distribution is limited to the Red
Mountain and Little Red Mountain areas
of Mendocino County, California, where
it occupies in excess of 81 acres, and
900 square feet, respectively. Occupied
habitat at Red Mountain is scattered
over 4 square miles. Total population
size has not been determined, but a
preliminary estimate suggests the
population may be in excess of 63,000
plants, occupying more than 44 discrete
habitat polygons. Intensive monitoring
of permanent plots on three study sites
in Red Mountain suggests considerable
annual variation in plant density and
reproduction, but no discernable
population trend was evident in two of
three study sites. One study site showed
a 65-percent decline in plant density
over 11 years.
The primary threat to this species is
the potential for surface mining for
chromium and nickel. Virtually the
entire distribution of Red Mountain
buckwheat is either owned by mining
interests, or is covered by existing
mining claims, none of which are
currently active. Surface mining would
destroy habitat suitability for this
species. The species is also believed
threatened by tree and shrub
encroachment into its habitat, due to the
absence of fire. Some 42 percent of its
known distribution occurred within the
boundary of the Red Mountain Fire of
June, 2008. However, the extent and
manner in which Eriogonum kelloggii
and its habitat were affected by that fire
is not yet known. The single population
located at Little Red Mountain appears
to have been affected, and perhaps
eliminated by fire-control efforts. The
known species distribution by
ownership is described as follows:
Federal (Bureau of Land Management),
83 percent; private, 17 percent; State of
California, less than 1 percent. Given
the magnitude (high) and immediacy
(nonimminent) of the threat to the
small, scattered populations, and its
taxonomy (species), we assigned a
listing priority number of 5 to this
species.
Festuca hawaiiensis (no common
name)—The following summary is
based on information contained in our
files. No new information was provided
in the petition we received on May 11,
2004. This species is a cespitose
(growing in dense, low tufts) annual
found in dry forest on the island of
Hawaii, Hawaii. Festuca hawaiiensis is
known from 4 populations totaling
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approximately 1,000 individuals in and
around the Pohakuloa Training Area.
Historically, this species was also found
on Hualalai and Puu Huluhulu, but it no
longer occurs at these sites.
Festuca hawaiiensis is threatened by
pigs, goats, mouflon, and sheep that
degrade and destroy habitat; fire;
military training activities; and
nonnative plants that outcompete and
displace it. Feral pigs, goats, mouflon,
and sheep have been fenced out of a
portion of the populations of F.
hawaiiensis, and nonnative plants have
been reduced in the fenced area, but the
majority of the populations are still
affected by threats from ungulates. The
threats are imminent because they are
not controlled and are ongoing in the
remaining, unfenced populations.
Firebreaks have been established at two
populations, but fire is an imminent
threat to the remaining populations that
have no firebreaks. The threats are of a
high magnitude because they could
adversely affect the majority of F.
hawaiiensis populations resulting in
direct mortality or reduced reproductive
capacity, leading to a relatively high
likelihood of extinction. Therefore, we
retained an LPN of 2 for this species.
Festuca ligulata (Guadalupe fescue)—
The following summary is based on
information obtained from the original
species petition, received in 1975, and
from our files, on-line herbarium
databases, and scientific publications.
Six small populations of Guadalupe
fescue, a member of the Poaceae (grass
family), have been documented in
mountains of the Chihuahuan desert in
Texas and in Coahuila, Mexico. Only
two extant populations have been
confirmed in the last 5 years, in the
Chisos Mountains, Big Bend National
Park, Texas, and in the privately owned
´
Area de Proteccion de Flora y Fauna
(Protected Area for Flora and Fauna—
APFF) Maderas del Carmen in northern
Coahuila. Despite intensive searches, a
population known from Guadalupe
Mountains National Park in Texas has
not been found since 1952 and is
presumed extirpated. In 2009, Mexican
botanists confirmed Guadalupe fescue at
one site in APFF Maderas del Carmen,
but could not find the species at the
´
original site, known as Sierra El Jardın,
which was first reported in 1973. Two
additional Mexican populations, near
Fraile in southern Coahuila, and the
Sierra de la Madera in central Coahuila,
have not been monitored since 1941 and
1977, respectively. A great amount of
potentially suitable habitat in Coahuila
has never been surveyed. The potential
threats to Guadalupe fescue include
changes in the wildfire cycle and
vegetation structure, trampling from
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humans and pack animals, grazing, trail
runoff, fungal infection of seeds, small
sizes and isolation of populations, and
limited genetic diversity. The Service
and the National Park Service
established a Candidate Conservation
Agreement in 2008 to provide
additional protection for the Chisos
Mountains population, and to promote
cooperative conservation efforts with
U.S. and Mexican partners. The threats
to Guadalupe fescue are of moderate
magnitude, and are not imminent, due
to the provisions of the Candidate
Conservation Agreement and other
conservation efforts, as well as the
likelihood that other populations exist
in mountains of Coahuila that have not
been surveyed. Thus, we maintained the
LPN of 11 for this species.
Gardenia remyi (Nanu)—The
following summary is based on
information contained in our files. No
new information was provided in the
petition we received on May 11, 2004.
Gardenia remyi is a tree found in mesic
to wet forest on the islands of Kauai,
Molokai, Maui, and Hawaii, Hawaii.
Gardenia remyi is known from 19
populations totaling between 85 and 87
individuals.
This species is threatened by pigs,
goats, and deer that degrade and destroy
habitat and possibly prey upon the
species, and by nonnative plants that
outcompete and displace it. Gardenia
remyi is also threatened by landslides
on the island of Hawaii. This species is
represented in ex situ collections. Feral
pigs have been fenced out of the west
Maui populations of G. remyi, and
nonnative plants have been reduced in
those areas. However, these threats are
not controlled and are ongoing in the
remaining, unfenced populations, and
are, therefore, imminent. In addition,
the threat from goats and deer is
ongoing and imminent throughout the
range of the species, because no goat or
deer control measures have been
undertaken for any of the populations of
G. remyi. All of the threats are of a high
magnitude because habitat destruction,
predation, and landslides could
significantly affect the entire species,
resulting in direct mortality or reduced
reproductive capacity, leading to a
relatively high likelihood of extinction.
Therefore, we retained an LPN of 2 for
this species.
Geranium hanaense (Nohoanu)—We
continue to find that listing this species
is warranted but precluded as of the
date of publication of this notice.
However, we are working on a proposed
listing rule that we expect to publish
prior to making the next annual
resubmitted 12-month petition finding.
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Geranium hillebrandii (Nohoanu)—
We continue to find that listing this
species is warranted but precluded as of
the date of publication of this notice.
However, we are working on a proposed
listing rule that we expect to publish
prior to making the next annual
resubmitted 12-month petition finding.
Gonocalyx concolor (no common
name)—The following summary is
based on information contained in our
files. No new information was provided
in the petition we received on May 11,
2004. Gonocalyx concolor is a small
evergreen epiphytic or terrestrial shrub.
Currently, G. concolor is known from
two populations in Puerto Rico: One at
Cerro La Santa and the other at Charco
Azul, both in the Carite Commonwealth
Forest. The forest is located in the Sierra
de Cayey and extends through the
municipalities of Guayama, Cayey,
Caguas, San Lorenzo, and Patillas in
southeastern Puerto Rico. The
population previously reported in the
Caribbean National Forest is apparently
no longer extant. In 1996, approximately
172 plants were reported at Cerro La
Santa. However, in 2006 only 25
individuals were reported at Cerro La
Santa and 4 individuals located at
Charco Azul.
The species is currently threatened by
habitat disturbance related to the
maintenance of existing
telecommunication facilities at Cerro La
Santa, limited distribution (2 sites) and
low population numbers (less than 30
individuals total), and hurricanes.
Although the species is located in the
Carite Commonwealth Forest, a public
forest managed by DNER, applicable
laws and regulations are not effectively
enforced and Service personnel has
documented damages to the population
located adjacent to existing
communication towers at the forest.
Because of extremely low population
numbers and the vulnerability to
current threats (maintenance activities
and hurricanes), the magnitude of
current threats on the species is high.
Overall, threats are nonimminent since
G. concolor is only known from the
Carite Commonwealth Forest,
administered and managed by the DNER
for conservation and recreation.
Therefore, we have assigned a listing
priority number of 5 for the Gonocalyx
concolor.
Hazardia orcuttii (Orcutt’s
hazardia)—The following summary is
based on information contained in our
files and the petition we received on
March 8, 2001. Hazardia orcuttii is an
evergreen shrubby species in the
Asteraceae (sunflower family). The erect
shrubs are 50–100 centimeters (20–40
inches) high. The only known extant
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native occurrence of this species in the
U.S. is in the Manchester Conservation
Area in northwestern San Diego County,
California. This site is managed by
Center for Natural Lands Management
(CNLM). Using material derived from
the native population, the CNLM
facilitated the establishment of test
populations at five additional sites in
northwest San Diego County, California,
including a second site in the
Manchester Conservation Area, Kelly
Ranch Habitat Conservation Area,
Rancho La Costa Habitat Conservation
Area, San Elijo Lagoon, and San Diego
Botanical Garden. Hazardia orcuttii also
occurs at a few coastal sites in Mexico,
where it has no conservation
protections. The total number of plants
at the only native site in the United
States is approximately 668 native adult
plants and 50 seedlings. The five
additional test populations collectively
support approximately 500 adult plants
and 350 seedlings.
The population in Mexico is
estimated to be 1300 plants. The
occurrences in Mexico are threatened by
coastal development from Tijuana to
Ensenada. The native population in the
U.S. is within an area that receives
public use; however, management at
this site has minimized impacts from
trampling, dumping, and other
unintentionally destructive impacts.
This species has a very low
reproductive output, although the
causes are as-yet unknown. Competition
from invasive nonnative plants may
pose a threat to the reproductive
potential of this species. In one study,
95 percent of the flowers examined were
damaged by insects or fungal agents or
aborted prematurely, and insects or
fungal agents damaged 50 percent of the
seeds produced. All of the populations
in the U.S. are small and two of the test
populations are declining. Small
populations are considered subject to
random events and reductions in fitness
due to low genetic variability. Threats
associated with small population size
are further exacerbated by the limited
range and low reproductive output of
this species. However, if low seed
production is because of ecosystem
disruptions, such as loss of effective
pollinators, there could be additional
threats that need to be addressed.
Overall, the threats to Hazardia orcuttii
are of a high magnitude because they
have the potential to significantly
reduce the reproductive potential of this
species. The threats are nonimminent
overall because the most significant
threats (invasive, nonnative plants and
low reproductive output) are
nonimminent and long-term in nature.
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This species faces high-magnitude
nonimminent threats; therefore, we
assigned this species a listing priority of
5.
Hedyotis fluviatilis (Kamapuaa)—The
following summary is based on
information contained in our files. No
new information was provided in the
petition we received on May 11, 2004.
Hedyotis fluviatilis is a scandent shrub
found in mixed shrubland to wet
lowland forest on the islands of Oahu
and Kauai, Hawaii. This species is
known from 11 populations totaling
between 400 and 900 individuals.
Hedyotis fluviatilis is threatened by pigs
and goats that degrade and destroy
habitat, and by nonnative plants that
outcompete and displace it. Landslides
are a potential threat to populations on
Kauai. Predation by pigs and goats is a
likely threat. This species is represented
in an ex situ collection; however, there
are no other conservation actions
implemented for this species. We
retained an LPN of 2 because the
severity of the threats to the species is
high and the threats are ongoing and,
therefore, imminent.
Helianthus verticillatus (Whorled
sunflower)—The following summary is
based on information contained in our
files. No new information was provided
in the petition we received on May 11,
2004. The whorled sunflower is found
in moist, prairie-like openings in
woodlands and along adjacent creeks.
Despite extensive surveys throughout its
range, only five populations are known
for this species. There are two
populations documented for Cherokee
County, Alabama; one population in
Floyd County, Georgia; and one
population each in Madison and
McNairy Counties, Tennessee. This
species appears to have restricted
ecological requirements and is
dependent upon the maintenance of
prairie-like openings for its survival.
Active management of habitat is needed
to keep competition and shading under
control. Much of its habitat has been
degraded or destroyed for agricultural,
silvicultural, and residential purposes.
Populations near roadsides or
powerlines are threatened by herbicide
usage in association with right-of-way
maintenance. The majority of the
Georgia population is protected due to
its location within a conservation
easement; however, only 15 to 20 plants
are estimated to occur at this site. The
remaining four sites are not formally
protected, but efforts have been taken to
abate threats associated with highway
right-of-way maintenance at one
Alabama population; and, despite past
concerns about threats from timber
removal degrading H. verticillatus
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habitat, the other Alabama population
has responded favorably to canopy
removal that took place circa 2001.
Therefore, threats are of moderate
magnitude, though imminent because
they are ongoing. Thus, we assigned this
species an LPN of 8.
Hibiscus dasycalyx (Neches River
rose-mallow)—See above in ‘‘Listing
Priority Changes in Candidates.’’ The
above summary is based on information
contained in our files.
Ivesia webberi (Webber ivesia)—The
following summary is based on
information contained in our files. No
new information was provided in the
petition we received on May 11, 2004.
Ivesia webberi is a low, spreading,
perennial herb that occurs very
infrequently in Lassen, Plumas, and
Sierra Counties in California, and in
Douglas and Washoe Counties, Nevada.
The species is restricted to sites with
sparse vegetation and shallow, rocky
soils composed of volcanic ash or
derived from andesitic rock (a gray, finegrained volcanic rock). Occupied sites
generally occur on mid-elevation flats,
benches, or terraces on mountain slopes
above large valleys along the transition
zone between the eastern edge of the
northern Sierra Nevada and the
northwestern edge of the Great Basin.
Currently, the global population is
estimated at approximately 5 million
individuals at 16 known sites. The
Nevada sites support nearly 98 percent
of the total number of individuals (4.9
million) on about 27 acres (11 hectares)
of occupied habitat. The California sites
are larger in area, totaling about 157
acres (63 hectares), but support fewer
individuals (approximately 120,000).
The primary threats to I. webberi
include urban development, authorized
and unauthorized roads, off-roadvehicle activities and other dispersed
recreation, livestock grazing and
trampling, fire and fire suppression
activities including fuels reduction and
prescribed fires, and displacement by
noxious weeds. Despite the high
numbers of individuals, observations in
2002 and 2004 confirmed that direct
and indirect impacts to the species and
its habitat, specifically from urban
development and off-highway-vehicle
activity remain high and are likely to
increase. However, the U.S. Forest
Service has developed a conservation
strategy that commits to management,
monitoring, and research to protect this
species on National Forest lands where
most populations are found, and the
State of Nevada has listed the species as
critically endangered, which provides a
mechanism to track future impacts on
private lands. In addition, both the U.S.
Forest Service and State of Nevada have
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agreed to coordinate closely with the
Fish and Wildlife Service on all
activities that may affect this species. In
light of these conservation
commitments, we have determined that
the threats to I. webberi are
nonimminent and are maintaining the
LPN of 5.
Joinvillea ascendens ssp. ascendens
(Ohe)—The following summary is based
on information contained in our files.
No new information was provided in
the petition we received on May 11,
2004. Joinvillea ascendens ssp.
ascendens is an erect herb found in wet
to mesic Metrosideros polymorphaAcacia koa (ohia-koa) lowland and
montane forest on the islands of Kauai,
Oahu, Molokai, Maui, and Hawaii,
Hawaii. This subspecies is known from
43 widely scattered populations totaling
fewer than 200 individuals. Plants are
typically found as only one or two
individuals, with miles between
populations. This subspecies is
threatened by destruction or
modification of habitat by pigs, goats,
and deer, and by nonnative plants that
outcompete and displace native plants.
Predation by pigs, goats, deer, and rats
is a likely threat to this species.
Landslides are a potential threat to
populations on Kauai and Molokai.
Seedlings have rarely been observed in
the wild. Seeds germinate in cultivation,
but most die soon thereafter. It is
uncertain if this rarity of reproduction is
typical of this subspecies, or if it is
related to habitat disturbance. Feral pigs
have been fenced out of a few of the
populations of this subspecies, and
nonnative plants have been reduced in
those populations that are fenced.
However, these threats are not
controlled and are ongoing in the
remaining, unfenced populations. This
species is represented in ex situ
collections. The threats are of high
magnitude because habitat degradation,
nonnative plants, and predation result
in mortality or severely affect the
reproductive capacity of the majority of
populations of this species, leading to a
relatively high probability of extinction.
The threats are ongoing, and thus are
imminent. Therefore, we retained an
LPN of 3 for this subspecies.
Korthalsella degeneri (Hulumoa)—We
continue to find that listing this species
is warranted but precluded as of the
date of publication of this notice.
However, we are working on a proposed
listing rule that we expect to publish
prior to making the next annual
resubmitted 12-month petition finding.
Leavenworthia crassa (Gladecress)—
The following information is based on
information contained in our files. No
new information was provided in the
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petition we received on May 11, 2004.
This species of gladecress is a
component of glade flora, occurring in
association with limestone
outcroppings. Leavenworthia crassa is
endemic to a 13-mile radius area in
north central Alabama in Lawrence and
Morgan Counties, where only six
populations of this species are
documented. Glade habitats today have
been reduced to remnants fragmented
by agriculture and development.
Populations of this species are now
located in glade-like areas exhibiting
various degrees of disturbance including
pastureland, roadside rights-of-way, and
cultivated or plowed fields. The most
vigorous populations of this species are
located in areas which receive full, or
near full, sunlight with limited
herbaceous competition. The magnitude
of threat is high for this species, because
with the limited number of populations,
the threats could result in direct
mortality or reduced reproductive
capacity of the species, leading to a
relatively high likelihood of extinction.
This species appears to be able to adjust
to periodic disturbances and the
potential impacts to populations from
competition, exotics, and herbicide use
are nonimminent. Thus, we assigned an
LPN of 5 to this species.
Leavenworthia texana (Texas golden
gladecress)—The following summary is
based on information contained in our
files. No new information was provided
in the petition we received on May 11,
2004. Leavenworthia texana occurs only
on the Weches outcrops of east Texas in
San Augustine and Sabine counties. The
Weches geologic formation consists of a
layer of calcareous sediment, lying
above a layer of glauconite clay
deposited up to 50 million years ago.
Erosion of this complex has produced
topography of steep, flat-topped hills
and escarpments, as well as the unique
ecology of Weches glades: Islands of
thin, loamy, seepy, alkaline soils that
support open-sun, herbaceous, and
highly diverse and specialized plant
communities.
Leavenworthia texana was
historically recorded at eight sites, all in
a narrow region along north San
Augustine and Sabine Counties. All
sites are on private land. Three sites
have been lost to glauconite mining and
two sites are currently closed to visitors.
The Sabine County site supported 1,000
plants within 9 square meters (97 square
feet) in 2007. The Tiger Creek site in
San Augustine County (less than 0.1
hectare (.2 acre) in size) was found to
have about 200 plants in 2007. The
Kardell site (less than 9 square meters
(97 square feet)) has supported 400–500
plants in past years, but none in 2005.
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An introduced population in
Nacogdoches County numbered about
1,000 within an area of about 18 square
meters (194 square feet) in 2007.
Historical habitat has been affected by
highway construction, residential
development, conversion to pasture and
cropland, widespread use of herbicide,
overgrazing, and glauconite mining.
However, the primary threat to existing
Leavenworthia texana populations is
the invasion of nonnative and weedy
shrubs and vines (primarily Macartney
rose (Rosa bracteata) and Japanese
honeysuckle (Lonicera japonica). All
known sites are undergoing severe
degradation by the incursion of
nonnative shrubs and vines, which
restrict both growth and reproduction of
the gladecress. Brushclearing carried out
in 1995 resulted in the reappearance of
L. texana after a 10-year absence at one
site. However, nonnative shrubs have
again invaded this area. More effective
control measures, such as burning and
selective herbicide use, need to be
tested and monitored. The small
number of known sites also makes L.
texana vulnerable to extreme natural
disturbance events. A severe drought in
1999 and 2000 had a pronounced
adverse effect on L. texana
reproduction. Since the threat from
nonnative plants severely affects all
known sites, the magnitude is high. The
threats are imminent since they are
ongoing. Therefore, we retain an LPN of
2 for L. texana.
Lesquerella globosa (Desvaux) Watson
(Short’s bladderpod)—The following
summary is based on information
contained in our files. No new
information was provided in the
petition we received on May 11, 2004.
Short’s bladderpod is a perennial
member of the mustard family that
occurs in Indiana (1 location), Kentucky
(6 locations), and Tennessee (22
locations). It grows on steep, rocky,
wooded slopes; on talus areas; along
cliff tops and bases; and on cliff ledges.
It is usually associated with south to
west facing calcareous outcrops adjacent
to rivers or streams. Road construction
and road maintenance have played a
significant role in the decline of L.
globosa. Specific activities that have
affected the species in the past and may
continue to threaten it include bank
stabilization, herbicide use, mowing
during the growing season, grading of
road shoulders, and road widening or
repaving. Sediment deposition during
road maintenance or from other
activities also potentially threatens the
species. Because the natural processes
that maintained habitat suitability and
competition from invasive nonnative
vegetation have been interrupted at
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many locations, active habitat
management is necessary at those sites.
While threats associated with roadside
maintenance activities and habitat
alterations by invasive plant
encroachment are imminent because
they are ongoing, this threat is of
moderate magnitude as they are not
affecting all locations of this species at
this time. Therefore, we assigned an
LPN of 8 to this species.
Linum arenicola (Sand flax)—See
above in ‘‘Listing Priority Changes in
Candidates.’’ That summary is based on
information contained in our files.
Linum carteri var. carteri (Carter’s
small-flowered flax)—The following
summary is based on information
contained in our files. No new
information was provided in the
petition we received on May 11, 2004.
This plant occupies open and disturbed
sites in pinelands of Miami-Dade
County, Florida. Currently, there are
nine known occurrences. Occurrences
with fewer than 100 individuals are
located on 3 county-owned preserves. A
site with more than 100 plants is owned
by the U.S. government, but the site is
not managed for conservation.
Climatic changes and sea level rise are
long-term threats that will likely reduce
the extent of habitat. The nine existing
occurrences are small and vulnerable to
habitat loss, which is exacerbated by
habitat degradation due to fire
suppression, the difficulty of applying
prescribed fire to pine rocklands, and
threats from exotic plants. Remaining
habitats are fragmented. Non-compatible
management practices are also a threat
at most protected sites; several sites are
mowed during the flowering and
fruiting season. In the absence of fire,
periodic mowing can, in some cases,
help maintain open, shrub-free
understory and provide benefits to this
plant. However, mowing can also
eliminate reproduction entirely in very
young plants, delay reproductive
maturation, and kill adult plants. With
flexibility in timing and proper
management, threats from mowing
practices can be reduced or negated.
Carter’s small-flowered flax is
vulnerable to natural disturbances, such
as hurricanes, tropical storms, and
storm surges. This species exists in such
small numbers at so few sites, that it
may be difficult to develop and
maintain viable occurrences on the
available conservation lands. Although
no population viability analysis has
been conducted for this plant,
indications are that existing occurrences
are at best marginal, and it is possible
that none are truly viable. As a result,
the magnitude of threats is high. The
threats are ongoing, and thus are
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imminent. Therefore, we assigned an
LPN of 3 to this plant variety.
Melicope christophersenii (Alani)—
We continue to find that listing this
species is warranted but precluded as of
the date of publication of this notice.
However, we are working on a proposed
listing rule that we expect to publish
prior to making the next annual
resubmitted 12-month petition finding.
Melicope hiiakae (Alani)—We
continue to find that listing this species
is warranted but precluded as of the
date of publication of this notice.
However, we are working on a proposed
listing rule that we expect to publish
prior to making the next annual
resubmitted 12-month petition finding.
Melicope makahae (Alani)—We
continue to find that listing this species
is warranted-but-precluded as of the
date of publication of this notice.
However, we are working on a proposed
listing rule that we expect to publish
prior to making the next annual
resubmitted 12-month petition finding.
Myrsine fosbergii (Kolea)—The
following summary is based on
information contained in our files. No
new information was provided in the
petition we received on May 11, 2004.
Myrsine fosbergii is a branched shrub or
small tree found in lowland mesic and
wet forest, on watercourses or stream
banks, on the islands of Kauai and
Oahu, Hawaii. This species is currently
known from 14 populations totaling a
little more than 100 individuals.
Myrsine fosbergii is threatened by feral
pigs and goats that degrade and destroy
habitat and may prey upon the plant,
and by nonnative plants that compete
for light and nutrients. This species is
represented in an ex situ collection.
Although there are plans to fence and
remove ungulates from the Helemano
area of Oahu, which may benefit this
species, no conservation measures have
been taken to date to alleviate these
threats for this species. Feral pigs and
goats are found throughout the known
range of M. fosbergii, as are nonnative
plants. The threats from feral pigs, goats,
and nonnative plants are of a high
magnitude because they pose a severe
threat throughout the limited range of
this species, and they are ongoing and
therefore imminent. We retained an LPN
of 2 for this species.
Myrsine vaccinioides (Kolea)—We
continue to find that listing this species
is warranted-but-precluded as of the
date of publication of this notice.
However, we are working on a proposed
listing rule that we expect to publish
prior to making the next annual
resubmitted 12-month petition finding.
Narthecium americanum (Bog
asphodel)—The following summary is
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based on information contained in our
files. No new information was provided
in the petition we received on May 11,
2004. Bog asphodel is a perennial herb
that is found in savanna areas, usually
with water moving through the
substrate, as well as in sandy bogs along
streams and rivers. The historical range
of bog asphodel included New York,
New Jersey, Delaware, North Carolina,
and South Carolina, although the
taxonomic identity of the historic North
Carolina specimens is now in question.
Extant populations of bog asphodel are
now only found within the Pine Barrens
region of New Jersey.
Curtailment of its historical range is a
primary threat to bog asphodel,
representing a loss of habitat and
genetic diversity and leaving the species
vulnerable to localized threats, natural
disasters, and climate change. The Pine
Barrens savannas that support bog
asphodel provide a scarce, specialized
habitat that has declined from several
thousand acres around 1900 to only a
thousand acres in recent decades. This
species has been lost from at least 3
States, and now occurs on less than 80
acres of land confined to an area only
about 30 miles in diameter. Of the 14
New Jersey watersheds that historically
supported bog asphodel, the species is
extirpated from six watersheds and
persists in four additional watersheds
only as a single occurrence. The 4
remaining watersheds are unevenly
distributed among the 3 river systems
supporting the species, with nearly 88
percent of bog asphodel (by area)
concentrated in the greater Mullica
River drainage.
Other significant threats include
unauthorized use of off-road vehicles,
future increases in water extraction for
human use, natural succession possibly
accelerated by fire suppression, and
potentially climate change. Lesser
threats include indirect effects of
upland development, impacts from
recreational activities, collection,
herbivory, and beaver activity. Because
the range of bog asphodel is currently
limited to New Jersey’s Pinelands Area
and Coastal Zone, regulatory protections
are generally adequate. More than 75
percent of bog asphodel occurs on
protected lands, although enforcement
of illegal activity can be lacking.
Outright habitat destruction from
wetland filling, draining, flooding, and
conversion to commercial cranberry
bogs likely contributed to the
curtailment of this species’ range, but
these historical threats to bog asphodel
are generally no longer occurring.
Current threats to bog asphodel are
low to moderate in magnitude. Several
threats are imminent because they are
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ongoing and expected to continue.
Overall, based on these imminent,
moderate threats, we retain a listing
priority number of 8 for this species.
Nothocestrum latifolium (’Aiea)—The
following summary is based on
information contained in our files. No
new information was provided in the
petition we received on May 11, 2004.
Nothocestrum latifolium is a small tree
found in dry to mesic forest on the
islands of Kauai, Oahu, Maui, Molokai,
and Lanai, Hawaii. Nothocestrum
latifolium is known from 17 steadily
declining populations totaling fewer
than 1,200 individuals.
This species is threatened by feral
pigs, goats, and axis deer that degrade
and destroy habitat and may prey upon
it; by nonnative plants that compete for
light and nutrients; and by the loss of
pollinators that negatively affect the
reproductive viability of the species.
This species is represented in an ex situ
collection. Ungulates have been fenced
out of four areas where N. latifolium
currently occurs, and nonnative plants
have been reduced in some populations
that are fenced. However, these ongoing
conservation efforts for this species
benefit only a few of the known
populations. The threats are not
controlled and are ongoing in the
remaining unfenced populations. In
addition, little regeneration is observed
in this species. The threats are of a high
magnitude, since they are severe enough
to affect the continued existence of the
species, leading to a relatively high
likelihood of extinction. The threats are
imminent, since they are ongoing.
Therefore, we retained an LPN of 2 for
this species.
Ochrosia haleakalae (Holei)—The
following summary is based on
information contained in our files. No
new information was provided in the
petition we received on May 11, 2004.
Ochrosia haleakalae is a tree found in
dry to mesic forest, often on lava, on the
islands of Hawaii and Maui, Hawaii.
This species is currently known from 8
populations totaling between 64 and 76
individuals.
Ochrosia haleakalae is threatened by
fire; by feral pigs, goats, and cattle that
degrade and destroy habitat and may
directly prey upon it; and by nonnative
plants that compete for light and
nutrients. This species is represented in
ex situ collections. Feral pigs, goats, and
cattle have been fenced out of one wild
and one outplanted population on
private lands on the island of Maui and
one outplanted population in Hawaii
Volcanoes National Park on the island
of Hawaii. Nonnative plants have been
reduced in the fenced areas. The threat
from fire is of a high magnitude and
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imminent because no control measures
have been undertaken to address this
threat that could adversely affect O.
haleakalae as a whole. The threats from
feral pigs, goats, and cattle are ongoing
to the unfenced populations of O.
haleakalae. The threat from nonnative
plants is ongoing and imminent and of
a high magnitude to the wild
populations on both islands as this
threat adversely affects the survival and
reproductive capacity of the majority of
the species, leading to a relatively high
likelihood of extinction. Therefore, we
retained an LPN of 2 for this species.
Pediocactus peeblesianus
var.fickeiseniae (Fickeisen plains
cactus)—The following summary is
based on information contained in our
files. No new information was provided
in the petition we received on May 11,
2004. Pediocactus peeblesianus var.
fickeiseniae is a small cactus known
from the Gray Mountain vicinity to the
Arizona strip in Coconino, Navajo, and
Mohave Counties, Arizona. The cactus
grows on exposed layers of Kaibab
limestone on canyon margins and welldrained hills in Navajoan desert or
grassland. In 1999, the Arizona Game
and Fish Department noted 23
occurrences for the species, including
historical ones. The species is located
on Bureau of Land Management (BLM),
U.S. Forest Service, tribal, and possibly
State lands. Recent reports from the
BLM and Navajo Nation describe
populations of the species as being in
decline. The main human-induced
threats to this cactus are activities
associated with road maintenance, offroad vehicles, and trampling associated
with livestock grazing. Monitoring data
has detected mortality associated with
livestock grazing. Illegal collection of
this species has been noted in the past,
but we do not know if it is a continuing
threat. The populations that have been
monitored have been affected, in part,
by the continuing drought. There has
been very low recruitment, and rabbits
and rodents have consumed adult plants
because there is reduced forage
available during these dry conditions.
Given that there are only a few known
populations, that the range of this taxon
is limited, and that the majority of the
known populations on BLM lands and
the Navajo Nation are experiencing
declines, we conclude that the threats
are of a high magnitude. The threats are
ongoing and, therefore, are imminent.
Thus, we have retained an LPN of 3 for
this plant variety.
Penstemon scariosus var. albifluvis
(White River beardtongue)—See above
in ‘‘Listing Priority Changes in
Candidates.’’ That summary is based on
information contained in our files.
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Peperomia subpetiolata (‘Ala ‘ala wai
nui)—We continue to find that listing
this species is warranted but precluded
as of the date of publication of this
notice. However, we are working on a
proposed listing rule that we expect to
publish prior to making the next annual
resubmitted 12-month petition finding.
Phyllostegia bracteata (no common
name)—We continue to find that listing
this species is warranted but precluded
as of the date of publication of this
notice. However, we are working on a
proposed listing rule that we expect to
publish prior to making the next annual
resubmitted 12-month petition finding.
Phyllostegia floribunda (no common
name)—The following summary is
based on information contained in our
files. No new information was provided
in the petition we received on May 11,
2004. This species is an erect subshrub
found in mesic to wet forest on the
island of Hawaii, Hawaii. This species
is known from 7 populations totaling
fewer than 25 individuals. Phyllostegia
floribunda is threatened by feral pigs
that degrade and destroy habitat, and by
nonnative plants that compete for light
and nutrients. This species is
represented in ex situ collections. The
National Park Service, The Nature
Conservancy, and the State have fenced
and outplanted more than 170
individuals at Olaa Forest Reserve, Kona
Hema, and Waiakea Forest Reserve
(more than 50, 20 individuals, and 100
individuals, respectively). Nonnative
plants have been reduced in these
fenced areas. However, no conservation
efforts have been implemented for the
unfenced populations. Overall, the
threats are moderate because
conservation efforts for over half of the
populations reduce the severity of the
threats. The threats are ongoing in the
unfenced portions and must be
constantly managed in the fenced
portions. Therefore, the threats are
imminent. We retained an LPN of 8
because the threats are of moderate
magnitude and are imminent for the
majority of the populations.
Physaria douglasii ssp. tuplashensis
(White Bluffs bladder-pod)—The
following summary is based on
information contained in our files. No
new information was provided in the
petition we received on May 11, 2004.
White Bluffs bladder-pod is a lowgrowing, herbaceous, short-lived,
perennial plant in the Brassicaceae
(mustard) family. Historically and
currently, White Bluffs bladder-pod is
only known from a single population
that occurs along the White Bluffs of the
Columbia River in Franklin County,
Washington. The entire range of the
species is a narrow band, approximately
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33 feet (10 meters) wide by 10.6 miles
(17 kilometers) long, at the upper edge
of the bluffs. The species occurs only on
cemented, highly alkaline, calcium
carbonate paleosol (a ‘‘caliche’’ soil) and
is believed to be a ‘‘calciphile.’’
Approximately 35 percent of the
known range of the species has been
moderately to severely affected by
landslides, an apparently permanent
destruction of the habitat. The entire
population of the species is down-slope
of irrigated agricultural land, the source
of the water seepage causing the mass
failures and landslides, but the southern
portion of the population is the closest
to the agricultural land and the most
affected by landslides. Other significant
threats include use of the habitat by
recreational off-road vehicles which
destroys plants, and the presence of
invasive nonnative plants that compete
with P. douglasii tuplashensis for
resources (light, water, nutrients).
Additionally, the increasing presence of
invasive nonnative plants may alter fire
regimes and potentially increase the
threat of fire to the P. douglasii
tuplashensis population. The threats to
the population from landslides and the
recreational off-road-vehicle use are
currently occurring and will continue to
occur in the future. In addition,
invasion by nonnative plants is
currently occurring, and with the 2007
fire that occurred in the area of the
existing population, invasive plants will
likely spread or increase throughout the
burned area of the population. We have
therefore determined that these threats
are imminent. Although approximately
35 percent of the population is severely
affected by landslides in the southern
portion of the range, the likelihood of
the persistence of the population in the
unaffected northern portion appears to
be fairly high. Currently, we know of no
plans to expand or significantly modify
the existing agriculture activities in
areas adjacent to the population. In
addition, deliberate modification of the
species’ immediate habitat is unlikely
due to its location and ownership (85
percent federal). Intermittent use of offroad vehicles does occur on the
Monument, although it is prohibited.
These activities are mainly confined to
the upper portion of the White Bluffs
where few P. douglasii tuplashensis
plants occur, so there is low to moderate
threat to the species from these
activities. Invasive plants are present in
the vicinity, but have not yet been
determined to be a significant problem.
As a result of the 2007 fire, there is a
higher probability that invasion of these
nonnatives will occur. While P.
douglasii tuplashensis is inherently
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vulnerable because it is a narrow
endemic, the magnitude of the ongoing
threats to the population is moderate;
therefore we retain an LPN of 9 for this
species.
Platanthera integrilabia (Correll) Leur
(White fringeless orchid)—The
following summary is based on
information contained in our files. No
new information was provided in the
petition we received on May 11, 2004.
Platanthera integrilabia is a perennial
herb that grows in partially, but not
fully, shaded, wet, boggy areas at the
head of streams and on seepage slopes
in Alabama, Georgia, Kentucky,
Mississippi, South Carolina and
Tennessee. Historically, there were at
least 90 populations of P. integrilabia. It
is presumed extirpated from North
Carolina and Virginia. Currently there
are about 50 extant sites supporting the
species.
Several populations have been
destroyed due to road, residential, and
commercial construction, and to
projects that altered soil and site
hydrology such that suitability for the
species was reduced. Several of the
known populations are in or adjacent to
powerline rights-of-way. Mechanical
clearing of these areas may benefit the
species by maintaining adequate light
levels; however, the indiscriminant use
of herbicides in these areas could pose
a significant threat to the species. Allterrain vehicles have damaged several
sites and pose a threat at most sites.
Most of the known sites for the species
occur in areas that are managed
specifically for timber production.
Timber management is not necessarily
incompatible with the protection and
management of the species, but care
must be taken during timber
management to ensure the hydrology of
bogs supporting the species is not
altered. Natural succession can result in
decreased light levels. Because of the
species dependence upon moderate-tohigh light levels, some type of active
management to prevent complete
canopy closure is required at most
locations. Collecting for commercial and
other purposes is a potential threat.
Herbivory (primarily deer) threatens the
species at several sites. Due to the
alteration of habitat and changes in
natural conditions, protection and
recovery of this species is dependent
upon active management rather than
just preservation of habitat. Invasive,
nonnative plants such as Japanese
honeysuckle and kudzu also threaten
several sites. The threats are
widespread; however, the impact of
those threats on the species survival is
moderate in magnitude. Several of the
sites are protected to some degree from
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the threats by being within State parks,
national forests, wildlife management
areas, or other protected land. The
threats however are imminent since
they are ongoing, and we have therefore
assigned an LPN of 8 to this species.
Platydesma cornuta var. cornuta (no
common name)—We continue to find
that listing this species is warranted but
precluded as of the date of publication
of this notice. However, we are working
on a proposed listing rule that we
expect to publish prior to making the
next annual resubmitted 12-month
petition finding.
Platydesma cornuta var. decurrens
(no common name)—We continue to
find that listing this species is
warranted but precluded as of the date
of publication of this notice. However,
we are working on a proposed listing
rule that we expect to publish prior to
making the next annual resubmitted
12-month petition finding.
Platydesma remyi (no common
name)—The following summary is
based on information contained in our
files. No new information was provided
in the petition we received on May 11,
2004. Platydesma remyi is a shrub or
shrubby tree found in wet forests on old
volcanic slopes on the island of Hawaii,
Hawaii. This species is known from 2
populations totaling fewer than 50
individuals. Platydesma remyi is
threatened by feral pigs and cattle that
degrade and destroy habitat, nonnative
plants that compete for light and
nutrients, reduced reproductive vigor,
and stochastic extinction due to
naturally occurring events. This species
is represented in an ex situ collection,
and by one individual included in a rare
plant exclosure in the Laupahoehoe
Natural Area Reserve. The threats are
ongoing and therefore imminent, and of
a high magnitude because of their
severity; the threats cause direct
mortality or significantly reduce the
reproductive capacity of the species
throughout its limited range, leading to
a relatively high likelihood of
extinction. Therefore, we retained an
LPN of 2 for this species.
Pleomele forbesii (Hala pepe)—We
continue to find that listing this species
is warranted-but-precluded as of the
date of publication of this notice.
However, we are working on a proposed
listing rule that we expect to publish
prior to making the next annual
resubmitted 12-month petition finding.
Potentilla basaltica (Soldier Meadow
cinquefoil or basalt cinquefoil)—The
following summary is based on
information contained in our files; the
petition we received on May 11, 2004,
provided no additional information on
the species. Potentilla basaltica is a low
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growing, rhizomatous, herbaceous
perennial that is associated with alkali
meadows, seeps, and occasionally
marsh habitats bordering perennial
thermal springs, outflows, and meadow
depressions. In Nevada, the species is
known only from Soldier Meadow in
Humboldt County. In northeastern
California, a single population occurs in
Lassen County. At Soldier Meadow,
there are 11 discrete known occurrences
within an area of about 24 acres (9.6
hectares) that support about 130,000
individuals. The California population
occurs on private and public land and
supports fewer than 1,000 plants. The
public land has been designated as an
Area of Critical Environmental Concern
by the Bureau of Land Management.
The species and its habitat are
threatened by recreational use in the
areas where it occurs as well as the
ongoing impacts of past water
diversions, livestock grazing, and offroad-vehicle travel. Conservation
measures implemented recently by the
Bureau of Land Management in Nevada
include the installation of fencing to
exclude livestock, wild horses, burros,
and other large mammals; the closure of
access roads to spring, riparian, and
wetland areas and the limiting of
vehicles to designated routes; the
establishment of a designated
campground away from the habitats of
sensitive species; the installation of
educational signage; and, an increased
staff presence, including law
enforcement, a volunteer site steward
during the 6-month period of peak
visitor use, and noxious weed control.
In California, public land management
actions include not allowing livestock
salting in the vicinity of springs, a
proposed long-term monitoring plot,
limitations on camping near springs,
withdrawal from salable mineral
leasing, recommendations to
withdrawal the land from mineral entry,
and noxious weed control treatments.
These conservation measures have
reduced the magnitude of threat to the
species to moderate; all remaining
threats are nonimminent and involve
long-term changes to the habitat for the
species resulting from past impacts.
Until a monitoring program is in place
that allows us to assess the long-term
trend of the species, we have assigned
an LPN of 11.
Pseudognaphalium (Gnaphalium
sandwicensium var. molokaiense
(Enaena)—The following summary is
based on information contained in our
files. No new information was provided
in the petition we received on May 11,
2004. Pseudognaphalium
sandwicensium var. molokaiense is a
perennial herb found in strand
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vegetation in dry consolidated dunes on
the islands of Molokai and Maui,
Hawaii. This variety is known from 5
populations totaling approximately 200
to 20,000 individuals (depending upon
rainfall) in the Moomomi area on the
island of Molokai, and from 2
populations of a few individuals at
Waiehu dunes and at Puu Kahulianapa
on west Maui. Pseudognaphalium
sandwicensium var. molokaiense is
threatened by feral goats and axis deer
that degrade and destroy habitat and
possibly prey upon it, and by nonnative
plants that compete for light and
nutrients. Potential threats also include
collection for lei-making, and off-road
vehicles that directly damage plants and
degrade habitat. Weed control protects
one population on Molokai; however,
no conservation efforts have been
initiated to date for the other
populations on Molokai or for the
individuals on Maui. This species is
represented in an ex situ collection. The
ongoing threats from feral goats, axis
deer, nonnative plants, collection, and
off-road vehicles are of a high
magnitude because no control measures
have been undertaken for the Maui
population or for the Molokai
populations, and the threats result in
direct mortality or significantly reduce
reproductive capacity for the majority of
the populations, leading to a relatively
high likelihood of extinction. Therefore,
we retained an LPN of 3 for this plant
variety.
Psychotria hexandra ssp. oahuensis
var. oahuensis (Kopiko)—We continue
to find that listing this species is
warranted-but-precluded as of the date
of publication of this notice. However,
we are working on a proposed listing
rule that we expect to publish prior to
making the next annual resubmitted
12-month petition finding.
Pteralyxia macrocarpa (Kaulu)—We
continue to find that listing this species
is warranted-but-precluded as of the
date of publication of this notice.
However, we are working on a proposed
listing rule that we expect to publish
prior to making the next annual
resubmitted 12-month petition finding.
Ranunculus hawaiensis (Makou)—
The following summary is based on
information contained in our files. No
new information was provided in the
petition we received on May 11, 2004.
Ranunculus hawaiensis is an erect or
ascending perennial herb found in
mesic to wet forest dominated by
Metrosideros polymorpha (ohia) and
Acacia koa (koa) with scree substrate
(loose stones or rocky debris on a slope)
on the islands of Maui and Hawaii,
Hawaii. This species is currently known
from 20 individuals in 5 populations on
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the island of Hawaii. One population on
Maui (Kukui planeze) was not relocated
on a survey conducted in 2006. In
addition, one wild population at
Waikamoi (also on Maui) has not been
observed since 1995. Ranunculus
hawaiensis is threatened by direct
predation by slugs, feral pigs, goats,
cattle, mouflon, and sheep; by pigs,
goats, cattle, mouflon, and sheep that
degrade and destroy habitat; and by
nonnative plants that compete for light
and nutrients. Three populations have
been outplanted into protected
exclosures; however, feral ungulates and
nonnative plants are not controlled in
the remaining, unfenced populations. In
addition, the threat from introduced
slugs is of a high magnitude because
slugs occur throughout the limited range
of this species and no effective measures
have been undertaken to control them or
prevent them from causing significant
adverse impacts to this species. Overall,
the threats from pigs, goats, cattle,
mouflon, sheep, slugs, and nonnative
plants are of a high magnitude, and
ongoing (imminent) for R. hawaiensis.
We retained an LPN of 2 for this species.
Ranunculus mauiensis (Makou)—The
following summary is based on
information contained in our files. No
new information was provided in the
petition we received on May 11, 2004.
Ranunculus mauiensis is an erect to
weakly ascending perennial herb found
in open sites in mesic to wet forest and
along streams on the islands of Maui,
Kauai, and Molokai, Hawaii. This
species is currently known from 14
populations totaling 198 individuals.
Ranunculus mauiensis is threatened by
feral pigs, goats, mule deer, axis deer,
and slugs that consume it; by habitat
degradation and destruction by feral
pigs, goats, and deer; and by nonnative
plants that compete for light and
nutrients. This species is represented in
ex situ collections. Feral pigs have been
fenced out of one Maui population of R.
mauiensis, and nonnative plants have
been reduced in the fenced area. One
individual occurs in the Kamakou
Preserve on Molokai, managed by The
Nature Conservancy. However, ongoing
conservation efforts benefit only two
populations. The threats are of high
magnitude and imminent because they
are ongoing in the Kauai and the
majority of the Maui populations.
Therefore, we retained an LPN of 2 for
this species.
Rorippa subumbellata (Tahoe yellow
cress)—The following summary is based
on information contained in our files
and the petition we received on
December 27, 2000. Rorippa
subumbellata is a small perennial herb
known only from the shores of Lake
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Tahoe in California and Nevada. Data
collected over the last 25 years generally
indicate that species occurrence
fluctuates yearly as a function of both
lake level and the amount of exposed
habitat. Records kept since 1900 show a
preponderance of years with high lake
levels that would isolate and reduce R.
subumbellata occurrences at higher
beach elevations. From the standpoint
of the species, less favorable peak years
have occurred almost twice as often as
more favorable low-level years. Annual
surveys are conducted to determine
population numbers, site occupancy,
and general disturbance regime. During
the 2003 and 2004 annual survey
period, the lake level was approximately
6,224 feet (ft) (1,898 meters (m)); 2004
was the fourth consecutive year of low
water. Rorippa subumbellata was
present at 45 of the 72 sites surveyed (65
percent occupied), up from 15 sites (19
percent occupied) in 2000 when the
lake level was high at 6,228 ft (1,898 m).
Approximately 25,200 stems were
counted or estimated in 2003, whereas
during the 2000 annual survey, the
estimated number of stems was 4,590.
Lake levels began to rise again in 2005
and less habitat was available. Lake
levels began to drop again in 2006
though 2008 leading to an increase in
both occupied sites and estimated stem
counts. During very low lake levels in
2009, an estimated 27,522 stems were
observed at 47 sites, equal to the highest
number of occupied sites previously
recorded.
Many Rorippa subumbellata sites are
intensively used for commercial and
public purposes and are subject to
various activities such as erosion
control, marina developments, pier
construction, and recreation. The U.S.
Forest Service, California Tahoe
Conservancy, and California Department
of Parks and Recreation have
management programs for R.
subumbellata that include monitoring,
fenced enclosures, and transplanting
efforts when funds and staff are
available. Public agencies (including the
Service), private landowners, and
environmental groups collaborated to
develop a conservation strategy coupled
with a Memorandum of UnderstandingConservation Agreement. The
conservation strategy, completed in
2003, contains goals and objectives for
recovery and survival, a research and
monitoring agenda, and serves as the
foundation for an adaptive management
program. Because of the continued
commitments to conservation
demonstrated by regulatory and land
management agencies participating in
the conservation strategy, we have
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determined the threats to R.
subumbellata from various land uses
have been reduced to a moderate
magnitude. In high-lake-level years such
as 2005, however, recreational use is
concentrated within R. subumbellata
habitat, and we consider this threat in
particular to be ongoing and imminent.
Therefore, we are maintaining an LPN of
8 for this species.
Schiedea pubescens (Maolioli)—The
following summary is based on
information contained in our files. No
new information was provided in the
petition we received on May 11, 2004.
Schiedea pubescens is a reclining or
weakly climbing vine found in diverse
mesic to wet forest on the islands of
Maui, Molokai, and Hawaii, Hawaii. It
is presumed extirpated from Lanai.
Currently, this species is known from 8
populations totaling between 30 and 32
individuals on Maui, from 4
populations totaling between 21 and 22
individuals on Molokai, and from 1
population of 4 to 6 individuals on the
island of Hawaii. Schiedea pubescens is
threatened by feral pigs and goats that
consume it and degrade and destroy
habitat, and by nonnative plants that
compete for light and nutrients. Feral
ungulates have been fenced out of the
population of S. pubescens on the
island of Hawaii. Feral goats have been
fenced out of a few of the west Maui
populations of S. pubescens. Nonnative
plants have been reduced in the
populations that are fenced on Maui.
However, the threats are not controlled
and are ongoing in the remaining
unfenced populations on Maui and the
four populations on Molokai. Fire is a
potential threat to the Hawaii Island
population. In light of the extremely low
number of individuals of this species,
the threats from goats and nonnative
plants are of a high magnitude because
they result in mortality and reduced
reproductive capacity for the majority of
the populations, leading to a relatively
high likelihood of extinction. The
threats are imminent because they are
ongoing with respect to most of the
populations. Therefore, we retained an
LPN of 2 for this species.
Schiedea salicaria (no common
name)—We continue to find that listing
this species is warranted but precluded
as of the date of publication of this
notice. However, we are working on a
proposed listing rule that we expect to
publish prior to making the next annual
resubmitted 12-month petition finding.
Sedum eastwoodiae (Red Mountain
stonecrop)—The following summary is
based on information contained in our
files and information provided by the
California Department of Fish and
Game. The petition we received on May
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11, 2004 provided no new information
on the species. Red Mountain stonecrop
is a perennial succulent which occupies
relatively barren, rocky openings and
cliffs in lower montane coniferous
forests, between 1,900 and 4,000 feet
elevation. Its distribution is limited to
Red Mountain, Mendocino County,
California, where it occupies in excess
of 54 acres scattered over 4 square
miles. Total population size has not
been determined, but a preliminary
estimate suggests the population may be
in excess of 29,000 plants, occupying
more than 27 discrete habitat polygons.
Intensive monitoring suggests
considerable annual variation in plant
seedling success and inflorescence
production.
The primary threat to the species is
the potential for surface mining for
chromium and nickel. The entire
distribution Red Mountain stonecrop is
either owned by mining interests, or is
covered by mining claims, none of
which are currently active. Surface
mining would destroy habitat suitability
for this species. The species is also
believed threatened by tree and shrub
encroachment into its habitat, in
absence of fire. Some 25 percent of its
known distribution occurred within the
boundary of the Red Mountain Fire of
June 2008. However, the extent and
manner in which Red Mountain
stonecrop and its habitat were affected
by that fire is not yet known. The
species distribution by ownership is
described as follows: Federal (Bureau of
Land Management), 95 percent; private,
5 percent. Given the magnitude (high)
and immediacy (non-imminent) of the
threat to the small, scattered
populations, and its taxonomy (species),
we assigned a listing priority number of
5 to this species.
Sicyos macrophyllus (‘Anunu)—The
following summary is based on
information contained in our files. No
new information was provided in the
petition we received on May 11, 2004.
Sicyos macrophyllus is a perennial vine
found in wet Metrosideros polymorpha
(ohia) forest and subalpine Sophora
chrysophylla-Myoporum sandwicense
(mamane-naio) forest. This species is
known from 10 populations totaling
between 24 and 26 individuals in the
Kohala and Mauna Kea areas, and in
Hawaii Volcanoes National Park (Puna
area) on the island of Hawaii, Hawaii. It
appears that a naturally occurring
population at Kipuka Ki in Hawaii
Volcanoes National Park is reproducing
by seeds, but seeds have not been
successfully germinated under nursery
conditions.
This species is threatened by feral
pigs, cattle, and mouflon sheep that
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degrade and destroy habitat, and by
nonnative plants that compete for light
and nutrients. This species is
represented in ex situ collections. Feral
pigs have been fenced out of some of the
areas where S. macrophyllus currently
occurs, but the fences do not exclude
sheep. Nonnative plants have been
reduced in the populations that are
fenced. However, the threats are not
controlled and are ongoing in the
remaining, unfenced populations, and
are, therefore, imminent. Similarly the
threat from mouflon sheep is ongoing
and imminent in all populations,
because the current fences do not
exclude sheep. In addition, all of the
threats are of a high magnitude because
habitat degradation and competition
from nonnative plants present a risk to
the species, resulting in direct mortality
or significantly reducing the
reproductive capacity, leading to a
relatively high likelihood of extinction.
Therefore, we retained an LPN of 2 for
this species.
Solanum nelsonii (popolo)—The
following summary is based on
information contained in our files. No
new information was provided in the
petition we received on May 11, 2004.
Solanum nelsonii is a sprawling or
trailing shrub found in coral rubble or
sand in coastal sites. This species is
known from populations on Molokai
(approximately 300 plants), the island of
Hawaii (5 plants), and the northwestern
Hawaiian Islands (NWHI), Hawaii. The
current populations in the NWHI are
found on Midway (approximately 260
plants), Laysan (approximately 490
plants), Pearl and Hermes (unknown
number of individuals), and Nihoa
(8,000 to 15,000 adult plants). On
Molokai, S. nelsonii is moderately
threatened by ungulates that degrade
and destroy habitat, and may eat S.
nelsonii. On Molokai and the NWHI,
this species is threatened by nonnative
plants that outcompete and displace it.
Solanum nelsonii is threatened by
predation by a nonnative grasshopper in
the NWHI. This species is represented
in ex situ collections. Ungulate
exclusion fences, routine fence
monitoring and maintenance, and weed
control protect the population of S.
nelsonii on Molokai. Limited weed
control is conducted in the NWHI.
These threats are of moderate magnitude
because of the relatively large number of
plants, and the fact that this species is
found on more than one island. The
threats are imminent for the majority of
the populations because they are
ongoing and are not being controlled.
We therefore retained an LPN of 8 for
this species.
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Sphaeralcea gierischii (Gierisch
mallow)—The following information is
based on information contained in our
files, including site visits by species
experts. There are nine known
populations of this species on a
combined total of approximately 59.5 ac
(24.12 ha) in Arizona and Utah. Seven
populations are found on approximately
55 ac (22.3 ha) managed by the Bureau
of Land Management in Arizona. One
population occurs on approximately 2
ac (0.81 ha) on land managed by the
Arizona State Land Department. One
population occurs on approximately 2.5
ac (1.01 ha) in Utah. The primary threat
to the species in Arizona is ongoing
gypsum mining and associated
activities. The primary threat to the
species in Utah is potential impacts
from off-road vehicle use. The threats
are high in magnitude, since survival of
the species is threatened throughout its
entire range in Arizona by gypsum
mining, with the two largest
populations in active mining operations.
Loss of those two populations would
significantly reduce the total number of
individuals throughout the range,
threatening the long-term viability of
this species. The threats are imminent,
since they are ongoing in Arizona.
Therefore, we assigned an LPN of 2 to
this species.
Stenogyne cranwelliae (no common
name)—The following summary is
based on information contained in our
files. No new information was provided
in the petition we received on May 11,
2004. Stenogyne cranwelliae is a
creeping vine found in wet forest
dominated by Metrosideros polymorpha
(ohia) on the island of Hawaii, Hawaii.
Stenogyne cranwelliae is known from 10
populations totaling fewer than 110
individuals. This species is threatened
by feral pigs that degrade and destroy
habitat, and by nonnative plants that
compete for light and nutrients. In
addition, S. cranwelliae is potentially
threatened by feral pigs and rats that
may directly prey upon it, and by
randomly occurring natural events such
as hurricanes and landslides. This
species is represented in an ex situ
collection. All of the threats are ongoing
rangewide, and no efforts for control or
eradication are being undertaken for
feral pigs, nonnative plants, or rats.
These threats significantly affect the
entire species particularly in light of its
small population size. We retained an
LPN of 2 because these imminent
threats are of a high magnitude.
Symphyotrichum georgianum
(Georgia aster)—The following summary
is based on information contained in
our files. No new information was
provided in the petition we received on
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May 11, 2004. Georgia aster is a relict
species of post oak savanna/prairie
communities that existed in the
southeast prior to widespread fire
suppression and extirpation of large
native grazing animals. Georgia aster
currently occurs in the States of
Alabama, Georgia, North Carolina and
South Carolina. The species is
presumed extant in 8 counties in
Alabama, 22 counties in Georgia, 9
counties in North Carolina, and 15
counties in South Carolina. The species
appears to have been eliminated from
Florida.
Most remaining populations survive
adjacent to roads, utility rights-of-way
and other openings where current land
management mimics natural
disturbance regimes. Most populations
are small (10–100 stems), and since the
species’ main mode of reproduction is
vegetative, each isolated population
may represent only a few genotypes.
Many populations are currently
threatened by one or more of the
following factors: Woody succession
due to fire suppression, development,
highway expansion or improvement,
and herbicide application. However, the
species is still relatively widely
distributed, and recent information
indicates the species is more abundant
than when we initially identified it as
a candidate for listing. Taking into
account its distribution and abundance,
the magnitude of threats is moderate.
Thus we assigned an LPN of 8 for this
species.
Zanthoxylum oahuense (Ae)—We
continue to find that listing this species
is warranted-but-precluded as of the
date of publication of this notice.
However, we are working on a proposed
listing rule that we expect to publish
prior to making the next annual
resubmitted 12-month petition finding.
Ferns and Allies
Christella boydiae (no common
name)—The following summary is
based on information contained in our
files. No new information was provided
in the petition we received on May 11,
2004. This species is a small- to
medium-sized fern found in mesic to
wet forest along stream banks on the
islands of Oahu and Maui, Hawaii.
Historically, this species was also found
on the island of Hawaii, but it has been
extirpated there. Currently, this species
is known from 7 populations totaling
approximately 300 individuals. This
species is threatened by feral pigs that
degrade and destroy habitat and may eat
this plant, and by nonnative plants that
compete for light and nutrients. Feral
pigs have been fenced out of the largest
population on Maui, and nonnative
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plants have been reduced in the fenced
area. No conservation efforts are under
way to alleviate threats to the other two
populations on Maui, or for the two
populations on Oahu. This species is
represented in an ex situ collection. The
magnitude of the threats acting upon the
currently extant populations is
moderate because the largest population
is protected from pigs, and nonnative
plants have been reduced in this area.
The threats are ongoing and therefore
imminent. Therefore, we retained an
LPN of 8 for this species.
Doryopteris takeuchii (no common
name)—We continue to find that listing
this species is warranted but precluded
as of the date of publication of this
notice. However, we are working on a
proposed listing rule that we expect to
publish prior to making the next annual
resubmitted 12-month petition finding.
Huperzia stemmermanniae
(Waewaeiole)—The following summary
is based on information contained in
our files. No new information was
provided in the petition we received on
May 11, 2004. This species is an
epiphytic pendant clubmoss found in
mesic-to-wet Metrosideros polymorphaAcacia koa (ohia-koa) forests on the
islands of Maui and Hawaii, Hawaii.
Only 3 populations are known, on Maui
and Hawaii, totaling approximately 30
individuals. The Maui population has
not been relocated since 1995. Huperzia
stemmermanniae is threatened by feral
pigs, goats, cattle, and axis deer that
degrade and destroy habitat, and by
nonnative plants that compete for light,
space, and nutrients. Huperzia
stemmermanniae is also threatened by
randomly occurring natural events due
to its small population size. One
individual at Waikamoi Preserve may
benefit from fencing for axis deer and
pigs. This species is represented in ex
situ collections. The threats from pigs,
goats, cattle, axis deer, and nonnative
plants are of a high magnitude because
they are sufficiently severe to adversely
affect the species throughout its limited
range, resulting in direct mortality or
significantly reducing reproductive
capacity, leading to a relatively high
likelihood of extinction. The threats are
imminent because they are ongoing.
Therefore, we retained an LPN of 2 for
this species.
Microlepia strigosa var. mauiensis
(Palapalai)—The following summary is
based on information contained in our
files. No new information was provided
in the petition we received on May 11,
2004. Microlepia strigosa var. mauiensis
is a terrestrial fern found in mesic-towet forests. It is currently found in
Hawaii on the islands of Maui, Oahu,
and Hawaii, from at least 9 populations
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totaling at least 50 individuals. There is
a possibility that the range of this plant
variety could be larger and include the
other main Hawaiian Islands.
Microlepia strigosa var. mauiensis is
threatened by feral pigs that degrade
and destroy habitat, and by nonnative
plants that compete for light and
nutrients. Pigs have been fenced out of
some areas on east and west Maui, and
on Hawaii, where M. strigosa var.
mauiensis currently occurs, and
nonnative plants have been reduced in
the fenced areas. However, the threats
are not controlled and are ongoing in
the remaining unfenced populations on
Maui, Oahu, and Hawaii. Therefore, the
threats from feral pigs and nonnative
plants are imminent. The threats are of
a high magnitude because they are
sufficiently severe to adversely affect
the species throughout its range,
resulting in direct mortality or
significantly reducing reproductive
capacity, leading to a relatively high
likelihood of extinction. We therefore
retained an LPN of 3 for M. strigosa var.
mauiensis.
Petitions To Reclassify Species Already
Listed or Add to the Listed Range
We previously made warranted-butprecluded findings on seven petitions
seeking to reclassify threatened species
to endangered status, and one petition
seeking to add New Mexico to the listed
range of the Canada lynx. The taxa
involved in the reclassification petitions
are three populations of the grizzly bear
(Ursus arctos horribilis), delta smelt
(Hypomesus transpacificus), the
spikedace (Meda fulgida), the loach
minnow (Tiaroga cobitis), and
Sclerocactus brevispinus (Pariette
cactus). Because these species are
already listed under the Act, they are
not candidates for listing and are not
included in Table 1. However, this
notice and associated species
assessment forms also constitute the
resubmitted petition findings for these
species. For the three grizzly bear
populations, we have not updated the
information in our assessments through
this notice as explained below.
Although we are completing an ongoing
review of the status of the grizzly bear
in the lower 48 States outside of the
Greater Yellowstone Areas (see below),
we continue to find that reclassification
to endangered for each of the three
populations (described below) is
warranted but precluded by work
identified above (see ‘‘Petition Findings
for Candidate Species’’). We also have
not updated the information in our
assessments for the spikedace and loach
minnow through this notice as
explained below. For delta smelt, we
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have not updated the information
included in the 12-month finding
(published April 7, 2010), which serves
as our assessment; we are currently
conducting a 5-year review, which will
provide updated information when we
complete it later this year. For
Sclerocactus brevispinus and Canada
lynx in New Mexico, our updated
assessments are provided below. We
find that reclassification to endangered
status for the delta smelt, spikedace,
loach minnow, and Sclerocactus
brevispinus and adding New Mexico to
the listed range of the Canada lynx are
all currently warranted but precluded
by work identified above (see ‘‘Petition
Findings for Candidate Species’’). One
of the primary reasons that the work
identified above is considered higher
priority is that the grizzly bear
populations, delta smelt, spikedace,
loach minnow, and Sclerocactus
brevispinus are currently listed as
threatened, and therefore already
receive certain protections under the
Act. We promulgated regulations
extending take prohibitions for
endangered species under section 9 to
threatened species (50 CFR 17.31).
Prohibited actions under section 9
include, but are not limited to, take (i.e.,
to harass, harm, pursue, hunt, shoot,
wound, kill, trap, capture, or collect, or
attempt to engage in such activity). For
plants, prohibited actions under section
9 include removing or reducing to
possession any listed plant from an area
under Federal jurisdiction (50 CFR
17.61). Other protections include those
under section 7(a)(2) of the Act whereby
Federal agencies must insure that any
action they authorize, fund, or carry out
is not likely to jeopardize the continued
existence of any endangered or
threatened species.
Grizzly bear (Ursus arctos horribilis)
North Cascades ecosystem, CabinetYaak, and Selkirk populations (Region
6)—We have not updated the
information in our uplisting findings
with regard to the grizzly bear (Ursus
arctos horribilis) populations in the
North Cascade, the Cabinet-Yaak, or the
Selkirk Ecosystems in this notice.
Between 1991 and 1999, we issued
warranted-but-precluded findings to
reclassify grizzly bears as endangered in
the North Cascades (56 FR 33892, July
24, 1991; 63 FR 30453, June 4, 1998),
the Cabinet-Yaak (58 FR 8250, February
12, 1993; 64 FR 26725, May 17, 1999),
and the Selkirk Ecosystems (64 FR
26725, May 17, 1999).
On April 18, 2007, We initiated a
5-year review to evaluate the current
status of grizzly bears in the lower 48
States (72 FR 19549–19551). This status
review will fully evaluate the biological
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conservation status of each population
according to the 5 factors in Section 4
of the Act. Although there is sufficient
evidence to support multiple DPSs
within the lower 48 State listing, we do
not intend to complete a DPS analysis
of each of these populations
individually within the 5-year review.
Instead, any DPS analyses would be
completed prior to or concurrent with
any rulemakings. We expect this 5-year
review to be completed in late 2010.
Delta smelt (Hypomesus
transpacificus) (Region 8) (see 75 FR
17667; April 7, 2010, for additional
information on why reclassification to
endangered is warranted but
precluded)—In March 2004, we
completed a 5-year review for delta
smelt in which we determined a change
in status from threatened to endangered
was not recommended. While none of
the threats, other than apparent
abundance, show significant differences
from 2004, we now have strong
evidence, not available at the time of
our 5-year review, that at least some of
those factors are endangering the
species. The primary evidence is the
continuing downward trend in delta
smelt abundance indices since a
significant decline that occurred in
2002. The most recent fall midwater
trawl abundance index is the lowest
ever recorded—less than one-tenth the
level it was in 2003. In addition, a 2005
population viability analysis calculated
a 50-percent likelihood that the species
could reach effective extinction (8,000
individuals) within 20 years.
There are many primary threats to the
species including: Direct entrainments
by State and Federal water export
facilities; summer and fall increases in
salinity and water clarity, and effects
from introduced species. Additional
threats are predation by striped and
largemouth bass and inland silversides,
entrainment into power plants,
contaminants, and small population
size. Existing regulatory mechanisms
have not proven adequate to halt the
decline of delta smelt since the time of
listing as a threatened species.
As a result of our analysis of the best
available scientific and commercial
information, we have assigned uplisting
the delta smelt an LPN of 2, based on
high magnitude and immediacy of
threats. The magnitude of the threats is
high, because they occur rangewide and
result in mortality or significantly
reduce the reproductive capacity of the
species, leading to a relatively high
likelihood of extinction. They are
imminent because these threats are
ongoing and, in some cases (e.g.,
nonnative species), considered
irreversible.
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Spikedace (Meda fulgida) (Region 2)—
We continue to find that uplisting this
species to endangered is warranted but
precluded as of the date of publication
of this notice. However, we are working
on a proposed uplisting rule, in
combination with a proposed
designation of critical habitat, that we
expect to publish prior to making the
next annual resubmitted 12-month
petition finding.
Loach minnow (Tiaroga cobitis)
(Region 2)—We continue to find that
uplisting this species to endangered is
warranted but precluded as of the date
of publication of this notice. However,
we are working on a proposed uplisting
rule, in combination with a proposed
designation of critical habitat, that we
expect to publish prior to making the
next annual resubmitted 12-month
petition finding.
Sclerocactus brevispinus (Pariette
cactus) (Region 6) (see 72 FR 53211,
September 18, 2007, and the species
assessment form (see ADDRESSES) for
additional information on why
reclassification to endangered is
warranted but precluded)—The Pariette
cactus is restricted to clay badlands of
the Wagon Hound member of the Uinta
Formation in the Uinta Basin of
northeastern Utah. The species is
restricted to one population with an
overall range of approximately 10 miles
by 5 miles in extent. The species’ entire
population is within a developed and
expanding oil and gas field. The
location of the species’ habitat exposes
it to destruction from road, pipeline,
and well-site construction in connection
with oil and gas development. The
species may be collected as a specimen
plant for horticultural use. Recreational
off-road vehicle use and livestock
trampling are additional potential
threats. The species is currently
federally listed as threatened by its
previous inclusion within the species
Sclerocactus glaucus. Based on current
information, we are assigning the
Pariette cactus the LPN of 6 for uplisting
to endangered. The threats are of a high
magnitude since any one of the threats
has the potential to severely affect this
species because it is a narrow endemic
species with a highly limited range and
distribution, but the threats are not
currently ongoing.
Canada lynx (Lynx canadensis) within
the State of New Mexico—In our finding
of December 17, 2009 (74 FR 66937), we
determined that lynx in New Mexico
were warranted for listing due to their
presence in the state as a result of the
Colorado reintroduction effort and we
assigned an LPN of 12 to amending the
listing of lynx to include New Mexico
in the listing. We reconfirm that
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assigning an LPN of 12 is appropriate
based on nonimminent threats of a low
magnitude to the lynx DPS. Humancaused mortality does not occur at a
level such that it creates a significant
threat to lynx in the contiguous United
States. The magnitude of threats to the
lynx DPS, inclusive of those lynx in
New Mexico, is low. The threats occur
infrequently and are nonimminent. We
do not consider lynx in New Mexico to
be essential to the survival or recovery
of the DPS. Furthermore, the amount of
suitable habitat for lynx in New Mexico
is considered negligible relative to the
amount of habitat within the listed
range. Potential impacts to the habitat
have not been documented to threaten
lynx, either in New Mexico or outside
of it. The areas outside the currently
listed area are not essential to the
conservation of the species. The
majority of lynx habitats within the
contiguous United States are already
protected by the Act. Because lynx in
the lower 48 are listed as a DPS, the
appropriate LPN for this level of
magnitude and immediacy of threats is
12.
Current Notice of Review
We gather data on plants and animals
native to the United States that appear
to merit consideration for addition to
the Lists of Endangered and Threatened
Wildlife and Plants. This notice
identifies those species that we
currently regard as candidates for
addition to the Lists. These candidates
include species and subspecies of fish,
wildlife, or plants and DPSs of
vertebrate animals. This compilation
relies on information from status
surveys conducted for candidate
assessment and on information from
State Natural Heritage Programs, other
State and Federal agencies,
knowledgeable scientists, public and
private natural resource interests, and
comments received in response to
previous notices of review.
Tables 1 and 2 list animals arranged
alphabetically by common names under
the major group headings, and list
plants alphabetically by names of
genera, species, and relevant subspecies
and varieties. Animals are grouped by
class or order. Plants are subdivided
into two groups: (1) Flowering plants
and (2) ferns and their allies. Useful
synonyms and subgeneric scientific
names appear in parentheses with the
synonyms preceded by an ‘‘equals’’ sign.
Several species that have not yet been
formally described in the scientific
literature are included; such species are
identified by a generic or specific name
(in italics), followed by ‘‘sp.’’ or ‘‘ssp.’’
We incorporate standardized common
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names in these notices as they become
available. We sort plants by scientific
name due to the inconsistencies in
common names, the inclusion of
vernacular and composite subspecific
names, and the fact that many plants
still lack a standardized common name.
Table 1 lists all candidate species,
plus species currently proposed for
listing under the Act. We emphasize
that in this notice we are not proposing
to list any of the candidate species;
rather, we will develop and publish
proposed listing rules for these species
in the future. We encourage State
agencies, other Federal agencies, and
other parties to give consideration to
these species in environmental
planning.
In Table 1, the ‘‘category’’ column on
the left side of the table identifies the
status of each species according to the
following codes:
PE—Species proposed for listing as
endangered. Proposed species are those
species for which we have published a
proposed rule to list as endangered or
threatened in the Federal Register. This
category does not include species for
which we have withdrawn or finalized
the proposed rule.
PT—Species proposed for listing as
threatened.
PSAT—Species proposed for listing as
threatened due to similarity of
appearance.
C—Candidates: Species for which we
have on file sufficient information on
biological vulnerability and threats to
support proposals to list them as
endangered or threatened. Issuance of
proposed rules for these species is
precluded at present by other higher
priority listing actions. This category
includes species for which we made a
12-month warranted-but-precluded
finding on a petition to list. We made
new findings on all petitions for which
we previously made ‘‘warranted-butprecluded’’ findings. We identify the
species for which we made a continued
warranted-but-precluded finding on a
resubmitted petition by the code ‘‘C*’’ in
the category column (see ‘‘Findings for
Petitioned Candidate Species’’ section
for additional information).
The ‘‘Priority’’ column indicates the
LPN for each candidate species, which
we use to determine the most
appropriate use of our available
resources. The lowest numbers have the
highest priority. We assign LPNs based
on the immediacy and magnitude of
threats as well as on taxonomic status.
We published a complete description of
our listing priority system in the
Federal Register (48 FR 43098,
September 21, 1983).
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The third column, ‘‘Lead Region,’’
identifies the Regional Office to which
you should direct information,
comments, or questions (see addresses
under Request for Information at the
end of the SUPPLEMENTARY INFORMATION
section).
Following the scientific name (fourth
column) and the family designation
(fifth column) is the common name
(sixth column). The seventh column
provides the known historical range for
the species or vertebrate population (for
vertebrate populations, this is the
historical range for the entire species or
subspecies and not just the historical
range for the distinct population
segment), indicated by postal code
abbreviations for States and U.S.
territories. Many species no longer
occur in all of the areas listed.
Species in Table 2 of this notice are
those we included either as proposed
species or as candidates in the previous
CNOR (published November 9, 2009)
that are no longer proposed species or
candidates for listing. Since November
9, 2009, we listed 54 species and
removed 1 species from candidate status
for the reason indicated by the code.
The first column indicates the present
status of each species, using the
following codes (not all of these codes
may have been used in this CNOR):
E—Species we listed as endangered.
T—Species we listed as threatened.
Rc—Species we removed from the
candidate list because currently
available information does not support
a proposed listing.
Rp—Species we removed from the
candidate list because we have
withdrawn the proposed listing.
The second column indicates why we
no longer regard the species as a
candidate or proposed species using the
following codes (not all of these codes
may have been used in this CNOR):
A—Species that are more abundant or
widespread than previously believed
and species that are not subject to the
degree of threats sufficient to warrant
continuing candidate status, or issuing a
proposed or final listing.
F—Species whose range no longer
includes a U.S. territory.
I—Species for which we have
insufficient information on biological
vulnerability and threats to support
issuance of a proposed rule to list.
L—Species we added to the Lists of
Endangered and Threatened Wildlife
and Plants.
M—Species we mistakenly included
as candidates or proposed species in the
last notice of review.
N—Species that are not listable
entities based on the Act’s definition of
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‘‘species’’ and current taxonomic
understanding.
U—Species that are not subject to the
degree of threats sufficient to warrant
issuance of a proposed listing or
continuance of candidate status due, in
part or totally, to conservation efforts
that remove or reduce the threats to the
species.
X—Species we believe to be extinct.
The columns describing lead region,
scientific name, family, common name,
and historical range include information
as previously described for Table 1.
Request for Information
We request you submit any further
information on the species named in
this notice as soon as possible or
whenever it becomes available. We are
particularly interested in any
information:
(1) Indicating that we should add a
species to the list of candidate species;
(2) Indicating that we should remove
a species from candidate status;
(3) Recommending areas that we
should designate as critical habitat for a
species, or indicating that designation of
critical habitat would not be prudent for
a species;
(4) Documenting threats to any of the
included species;
(5) Describing the immediacy or
magnitude of threats facing candidate
species;
(6) Pointing out taxonomic or
nomenclature changes for any of the
species;
(7) Suggesting appropriate common
names; and
(8) Noting any mistakes, such as
errors in the indicated historical ranges.
Submit information, materials, or
comments regarding a particular species
to the Regional Director of the Region
identified as having the lead
responsibility for that species. The
regional addresses follow:
Region 1. Hawaii, Idaho, Oregon,
Washington, American Samoa, Guam,
and Commonwealth of the Northern
Mariana Islands. Regional Director (TE),
U.S. Fish and Wildlife Service, Eastside
Federal Complex, 911 NE. 11th Avenue,
Portland, OR 97232–4181 (503/231–
6158).
Region 2. Arizona, New Mexico,
Oklahoma, and Texas. Regional Director
(TE), U.S. Fish and Wildlife Service, 500
Gold Avenue, SW., Room 4012,
Albuquerque, NM 87102 (505/248–
6920).
Region 3. Illinois, Indiana, Iowa,
Michigan, Minnesota, Missouri, Ohio,
and Wisconsin. Regional Director (TE),
U.S. Fish and Wildlife Service, Bishop
Henry Whipple Federal Building, One
Federal Drive, Fort Snelling, MN 55111–
4056 (612/713–5334).
Region 4. Alabama, Arkansas, Florida,
Georgia, Kentucky, Louisiana,
Mississippi, North Carolina, South
Carolina, Tennessee, Puerto Rico, and
the U.S. Virgin Islands. Regional
Director (TE), U.S. Fish and Wildlife
Service, 1875 Century Boulevard, Suite
200, Atlanta, GA 30345 (404/679–4156).
Region 5. Connecticut, Delaware,
District of Columbia, Maine, Maryland,
Massachusetts, New Hampshire, New
Jersey, New York, Pennsylvania, Rhode
Island, Vermont, Virginia, and West
Virginia. Regional Director (TE), U.S.
Fish and Wildlife Service, 300 Westgate
Center Drive, Hadley, MA 01035–9589
(413/253–8615).
Region 6. Colorado, Kansas, Montana,
Nebraska, North Dakota, South Dakota,
Utah, and Wyoming. Regional Director
(TE), U.S. Fish and Wildlife Service,
P.O. Box 25486, Denver Federal Center,
Denver, CO 80225–0486 (303/236–
7400).
Region 7. Alaska. Regional Director
(TE), U.S. Fish and Wildlife Service,
1011 East Tudor Road, Anchorage, AK
99503–6199 (907/786–3505).
Region 8. California and Nevada.
Regional Director (TE), U.S. Fish and
Wildlife Service, 2800 Cottage Way,
Suite W2606, Sacramento, CA 95825
(916/414–6464).
We will provide information received
in response to the previous CNOR to the
Region having lead responsibility for
each candidate species mentioned in the
submission. We will likewise consider
all information provided in response to
this CNOR in deciding whether to
propose species for listing and when to
undertake necessary listing actions
(including whether emergency listing
pursuant to section 4(b)(7) of the Act is
appropriate). Information and comments
we receive will become part of the
administrative record for the species,
which we maintain at the appropriate
Regional Office.
Before including your address, phone
number, e-mail address, or other
personal identifying information in your
submission, be advised that your entire
submission—including your personal
identifying information—may be made
publicly available at any time. Although
you can ask us in your submission to
withhold from public review your
personal indentifying information, we
cannot guarantee that we will be able to
do so.
Authority: This notice is published under
the authority of the Endangered Species Act
(16 U.S.C. 1531 et seq.).
Dated: October 22, 2010.
Rowan W. Gould,
Acting Director, Fish and Wildlife Service.
TABLE 1—CANDIDATE NOTICE OF REVIEW (ANIMALS AND PLANTS)
[Note: See end of SUPPLEMENTARY INFORMATION for an explanation of symbols used in this table.]
Status
Category
Lead
region
Priority
2
3
R4
R1
C* ......................
jlentini on DSKJ8SOYB1PROD with PROPOSALS3
MAMMALS:
C* ......................
C* ......................
3
R1
C* ......................
2
R5
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Scientific name
Family
Common name
Eumops floridanus .....
Emballonura
semicaudata
rotensis.
Emballonura
semicaudata
semicaudata.
Sylvilagus
transitionalis.
Molossidae .................
Emballonuridae ..........
Bat, Florida bonneted
Bat, Pacific sheathtailed (Mariana Islands subspecies).
Bat, Pacific sheathtailed (American
Samoa DPS).
Cottontail, New England.
PO 00000
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Fmt 4701
Emballonuridae ..........
Leporidae ...................
Sfmt 4702
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10NOP3
Historical range
U.S.A. (FL).
U.S.A. (GU, CNMI).
U.S.A. (AS), Fiji, Independent Samoa,
Tonga, Vanuatu.
U.S.A. (CT, MA, ME,
NH, NY, RI, VT).
Federal Register / Vol. 75, No. 217 / Wednesday, November 10, 2010 / Proposed Rules
69285
TABLE 1—CANDIDATE NOTICE OF REVIEW (ANIMALS AND PLANTS)—Continued
[Note: See end of SUPPLEMENTARY INFORMATION for an explanation of symbols used in this table.]
Status
Category
Lead
region
Priority
Scientific name
Family
Common name
Historical range
6
R8
Martes pennanti .........
Mustelidae ..................
Fisher (west coast
DPS).
C* ......................
3
R2
3
R1
C .......................
3
R1
C* ......................
3
R1
C* ......................
3
R1
C* ......................
3
R1
C* ......................
3
R1
C* ......................
3
R1
C* ......................
3
R1
Geomyidae .................
Mouse, New Mexico
meadow jumping.
Pocket gopher,
Shelton.
Pocket gopher, Brush
Prairie.
Pocket gopher, Roy
Prairie.
Pocket gopher,
Cathlamet.
Pocket gopher, Olympic.
Pocket gopher, Olympia.
Pocket gopher, Tacoma.
Pocket gopher, Tenino
U.S.A. (WA).
C* ......................
3
R1
Geomyidae .................
Pocket gopher, Yelm
U.S.A. (WA).
C* ......................
3
R6
Zapus hudsonius
luteus.
Thomomys mazama
couchi.
Thomomys mazama
douglasii.
Thomomys mazama
glacialis.
Thomomys mazama
louiei.
Thomomys mazama
melanops.
Thomomys mazama
pugetensis.
Thomomys mazama
tacomensis.
Thomomys mazama
tumuli.
Thomomys mazama
yelmensis.
Cynomys gunnisoni ...
Zapodidae ..................
C* ......................
Sciuridae ....................
9
R1
Sciuridae ....................
C* ......................
5
R1
Spermophilus
brunneus
endemicus.
Spermophilus
washingtoni.
Prairie dog, Gunnison’s (central and
south-central Colorado, north-central
New Mexico SPR).
Squirrel, Southern
Idaho ground.
U.S.A. (CO, NM).
C* ......................
Sciuridae ....................
Squirrel, Washington
ground.
U.S.A. (WA, OR).
BIRDS:
C* ......................
3
R1
Porzana tabuensis .....
Rallidae ......................
Crake, spotless
(American Samoa
DPS).
C* ......................
3
R8
Coccyzus americanus
Cuculidae ...................
C* ......................
9
R1
Gallicolumba stairi .....
Columbidae ................
C* ......................
3
R1
3
R5
Eremophila alpestris
strigata.
Calidris canutus rufa ..
Alaudidae ...................
C* ......................
Scolopacidae .............
C* ......................
jlentini on DSKJ8SOYB1PROD with PROPOSALS3
C* ......................
8
R7
Gavia adamsii ............
Gaviidae .....................
C* ......................
2
R7
Alcidae .......................
C* ......................
5
R8
Brachyramphus
brevirostris.
Synthliboramphus
hypoleucus.
U.S.A. (AS), Australia,
Fiji, Independent
Samoa, Marquesas,
Philippines, Society
Islands, Tonga.
Cuckoo, yellow-billed
U.S.A. (Lower 48
(Western U.S. DPS).
States), Canada,
Mexico, Central and
South America.
Ground-dove, friendly
U.S.A. (AS), Inde(American Samoa
pendent Samoa.
DPS).
Horned lark, streaked
U.S.A. (OR, WA),
Canada (BC).
Knot, red .................... U.S.A. (Atlantic coast),
Canada, South
America.
Loon, yellow-billed ..... U.S.A. (AK), Canada,
Norway, Russia,
coastal waters of
southern Pacific and
North Sea.
Murrelet, Kittlitz’s ....... U.S.A. (AK), Russia.
Alcidae .......................
Murrelet, Xantus’s ......
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Geomyidae .................
Geomyidae .................
Geomyidae .................
Geomyidae .................
Geomyidae .................
Geomyidae .................
Geomyidae .................
Sfmt 4702
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10NOP3
U.S.A. (CA, CT, IA,
ID, IL, IN, KY, MA,
MD, ME, MI, MN,
MT, ND, NH, NJ,
NY, OH, OR, PA,
RI, TN, UT, VA, VT,
WA, WI, WV, WY),
Canada.
U.S.A. (AZ, CO, NM).
U.S.A. (WA).
U.S.A. (WA).
U.S.A. (WA).
U.S.A. (WA).
U.S.A. (WA).
U.S.A. (WA).
U.S.A. (WA).
U.S.A. (ID).
U.S.A. (CA), Mexico.
69286
Federal Register / Vol. 75, No. 217 / Wednesday, November 10, 2010 / Proposed Rules
TABLE 1—CANDIDATE NOTICE OF REVIEW (ANIMALS AND PLANTS)—Continued
[Note: See end of SUPPLEMENTARY INFORMATION for an explanation of symbols used in this table.]
Status
Category
Lead
region
Priority
Scientific name
Family
Common name
Historical range
2
R6
Anthus spragueii ........
Motacillidae ................
Pipit, Sprauge’s ..........
PT .....................
—
R6
Charadrius montanus
Charadriidae ..............
Plover, mountain ........
C* ......................
2
R2
Prairie-chicken, lesser
8
R6
Tympanuchus
pallidicinctus.
Centrocercus
urophasianus.
Phasianidae ...............
C* ......................
Phasianidae ...............
Sage-grouse, greater
C* ......................
3
R8
Centrocercus
urophasianus.
Phasianidae ...............
Sage-grouse, greater
(Bi-State DPS).
C* ......................
6
R1
Centrocercus
urophasianus.
Phasianidae ...............
Sage-grouse, greater
(Columbia Basin
DPS).
C* ......................
2
R6
Centrocercus minimus
Phasianidae ...............
C* ......................
3
R1
Oceanodroma castro
Hydrobatidae ..............
Sage-grouse, Gunnison.
Storm-petrel, bandrumped (Hawaii
DPS).
C* ......................
REPTILES:
C* ......................
11
R4
Dendroica angelae .....
Emberizidae ...............
Warbler, elfin-woods ..
U.S.A. (AL, AR, AZ,
CA, GA, LA, MA,
MI, MN, MS, MT,
ND, OH, OK, SC,
SD, TX), Canada,
Mexico.
U.S.A. (AZ, CA, CO,
KS, MT, ND, NE,
NM, NN, OK, SD,
TX, UT, WY), Canada (AB, SK), Mexico.
U.S.A. (CO, KA, NM,
OK, TX).
U.S.A. (AZ, CA, CO,
ID, MT, ND, NE,
NV, OR, SD, UT,
WA, WY), Canada
(AB, BC, SK).
U.S.A. (AZ, CA, CO,
ID, MT, ND, NE,
NV, OR, SD, UT,
WA, WY), Canada
(AB, BC, SK).
U.S.A. (AZ, CA, CO,
ID, MT, ND, NE,
NV, OR, SD, UT,
WA, WY), Canada
(AB, BC, SK).
U.S.A. (AZ, CO, NM,
UT).
U.S.A. (HI), Atlantic
Ocean, Ecuador
(Galapagos Islands), Japan.
U.S.A. (PR).
3
R2
2
9
R2
R3
Thamnophis eques
megalops.
Sceloporus arenicolus
Sistrurus catenatus
catenatus.
Colubridae ..................
C* ......................
C* ......................
C* ......................
3
R4
Colubridae ..................
U.S.A. (AZ, NM, NV),
Mexico.
U.S.A. (TX, NM).
U.S.A. (IA, IL, IN, MI,
MO, MN, NY, OH,
PA, WI), Canada.
U.S.A. (AL, LA, MS).
5
3
R4
R2
Colubridae ..................
Colubridae ..................
3
R2
Snake, Louisiana pine
Snake, Tucson shovel-nosed.
Turtle, Sonoyta mud ..
U.S.A. (LA, TX).
U.S.A. (AZ).
C* ......................
Pituophis
melanoleucus
lodingi.
Pituophis ruthveni ......
Chionactis occipitalis
klauberi.
Kinosternon
sonoriense
longifemorale.
Gartersnake, northern
Mexican.
Lizard, sand dune ......
Massasauga
(=rattlesnake), eastern.
Snake, black pine ......
C* ......................
C* ......................
AMPHIBIANS:
C* ......................
9
R8
Rana luteiventris ........
Ranidae ......................
C* ......................
jlentini on DSKJ8SOYB1PROD with PROPOSALS3
C* ......................
3
R8
Rana muscosa ...........
Ranidae ......................
U.S.A. (AK, ID, MT,
NV, OR, UT, WA,
WY), Canada (BC).
U.S.A. (CA, NV).
C* ......................
2
R1
Rana pretiosa ............
Ranidae ......................
Frog, Columbia spotted (Great Basin
DPS).
Frog, mountain yellow-legged (Sierra
Nevada DPS).
Frog, Oregon spotted
C* ......................
PE .....................
11
3
R8
R3
Ranidae ......................
Crytobranchidae .........
Frog, relict leopard .....
Hellbender, Ozark ......
C* ......................
2
R2
Lithobates onca .........
Cryptobranchus
alleganiensis
bishopi.
Eurycea waterlooensis
Plethodontidae ...........
Salamander, Austin
blind.
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Iguanidae ...................
Viperidae ....................
Kinosternidae .............
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10NOP3
U.S.A. (AZ), Mexico.
U.S.A. (CA, OR, WA),
Canada (BC).
U.S.A. (AZ, NV, UT).
U.S.A. (AR, MO).
U.S.A. (TX).
Federal Register / Vol. 75, No. 217 / Wednesday, November 10, 2010 / Proposed Rules
69287
TABLE 1—CANDIDATE NOTICE OF REVIEW (ANIMALS AND PLANTS)—Continued
[Note: See end of SUPPLEMENTARY INFORMATION for an explanation of symbols used in this table.]
Status
Category
Lead
region
Priority
Scientific name
Family
Common name
Salamander, Georgetown.
Salamander, Jemez
Mountains.
Salamander, Jollyville
Plateau.
Salamander, Salado ..
C* ......................
8
R2
Eurycea naufragia ......
Plethodontidae ...........
C* ......................
2
R2
Plethodontidae ...........
C* ......................
8
R2
Plethodon
neomexicanus.
Eurycea tonkawae .....
C* ......................
2
R2
C* ......................
C .......................
11
3
C* ......................
Plethodontidae ...........
R8
R2
Eurycea
chisholmensis.
Bufo canorus ..............
Hyla wrightorum .........
Plethodontidae ...........
Bufonidae ...................
Hylidae .......................
8
R4
Necturus alabamensis
Proteidae ....................
FISHES:
C* ......................
C* ......................
8
7
R2
R6
C* ......................
9
R2
Gila nigra ...................
Iotichthys
phlegethontis.
Gila robusta ...............
PE .....................
C* ......................
5
11
R4
R6
Phoxinus saylori .........
Etheostoma cragini ....
PE .....................
C .......................
5
2
R4
R5
C .......................
3
R4
C* ......................
PE .....................
8
2
R4
R4
PE .....................
C* ......................
2
3
R4
R6
PE .....................
C .......................
C* ......................
C* ......................
C* ......................
C* ......................
2
5
2
5
5
3
R4
R4
R3
R2
R2
R2
PSAT ................
N/A
R1
C* ......................
9
CLAMS:
C .......................
PE .....................
Historical range
U.S.A. (TX).
U.S.A. (NM).
U.S.A. (TX).
U.S.A. (TX).
Toad, Yosemite ..........
Treefrog, Arizona
(Huachuca/Canelo
DPS).
Waterdog, black warrior (=Sipsey Fork).
U.S.A. (CA).
U.S.A. (AZ), Mexico
(Sonora).
Cyprinidae ..................
Cyprinidae ..................
Chub, headwater .......
Chub, least .................
U.S.A. (AZ, NM).
U.S.A. (UT).
Cyprinidae ..................
U.S.A. (AZ, CO, NM,
UT, WY).
Cyprinidae ..................
Percidae .....................
Chub, roundtail
(Lower Colorado
River Basin DPS).
Dace, laurel ................
Darter, Arkansas ........
Etheostoma susanae
Crystallaria cincotta ...
Percidae .....................
Percidae .....................
Darter, Cumberland ...
Darter, diamond .........
Etheostoma sagitta
spilotum.
Percina aurora ...........
Etheostoma
phytophilum.
Etheostoma moorei ....
Thymallus arcticus .....
Percidae .....................
Darter, Kentucky
arrow.
Darter, Pearl ..............
Darter, rush ................
Percidae .....................
Percidae .....................
U.S.A. (TN).
U.S.A. (AR, CO, KS,
MO, OK).
U.S.A. (KY, TN).
U.S.A. (KY, OH, TN,
WV).
U.S.A. (KY).
U.S.A. (LA, MS).
U.S.A. (AL).
Ictaluridae ..................
Catostomidae .............
Cottidae ......................
Cyprinidae ..................
Cyprinidae ..................
Catostomidae .............
Salmonidae ................
Trout, Dolly Varden ....
R2
Oncorhynchus clarki
virginalis.
Salmonidae ................
Trout, Rio Grande cutthroat.
5
2
R4
R3
Villosa choctawensis ..
Villosa fabalis .............
Unionidae ...................
Unionidae ...................
Bean, Choctaw ..........
Bean, rayed ...............
C .......................
C* ......................
2
8
R4
R2
Fusconaia rotulata .....
Popenaias popei ........
Unionidae ...................
Unionidae ...................
Ebonyshell, round ......
Hornshell, Texas ........
C* ......................
jlentini on DSKJ8SOYB1PROD with PROPOSALS3
Noturus crypticus .......
Moxostoma sp ...........
Cottus sp ....................
Notropis oxyrhynchus
Notropis buccula ........
Catostomus
discobolus yarrowi.
Salvelinus malma .......
Darter, yellowcheek ... U.S.A. (AR).
Grayling, Arctic (upper U.S.A. (AK, MI, MT,
Missouri River DPS).
WY), Canada,
northern Asia,
northern Europe.
Madtom, chucky ......... U.S.A. (TN).
Redhorse, sicklefin .... U.S.A. (GA, NC, TN).
Sculpin, grotto ............ U.S.A. (MO).
Shiner, sharpnose ...... U.S.A. (TX).
Shiner, smalleye ........ U.S.A. (TX).
Sucker, Zuni bluehead U.S.A. (AZ, NM).
2
R4
Unionidae ...................
Kidneyshell, fluted ......
C .......................
C* ......................
2
2
R4
R4
Unionidae ...................
Unionidae ...................
Kidneyshell, southern
Mucket, Neosho .........
C .......................
2
R3
Ptychobranchus
subtentum.
Ptychobranchus jonesi
Lampsilis
rafinesqueana.
Plethobasus cyphyus
Unionidae ...................
Mussel, sheepnose ....
C* ......................
2
R4
Margaritifera
marrianae.
Margaritiferidae ..........
Pearlshell, Alabama ...
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Percidae .....................
Salmonidae ................
U.S.A. (AL).
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10NOP3
U.S.A. (AK, WA),
Canada, East Asia.
U.S.A. (CO, NM).
U.S.A. (AL, FL).
U.S.A. (IL, IN, KY, MI,
NY, OH, TN, PA,
VA, WV), Canada
(ON).
U.S.A. (AL, FL).
U.S.A. (NM, TX), Mexico.
U.S.A. (AL, KY, TN,
VA).
U.S.A. (AL, FL).
U.S.A. (AR, KS, MO,
OK).
U.S.A. (AL, IA, IL, IN,
KY, MN, MO, MS,
OH, PA, TN, VA,
WI, WV).
U.S.A. (AL).
69288
Federal Register / Vol. 75, No. 217 / Wednesday, November 10, 2010 / Proposed Rules
TABLE 1—CANDIDATE NOTICE OF REVIEW (ANIMALS AND PLANTS)—Continued
[Note: See end of SUPPLEMENTARY INFORMATION for an explanation of symbols used in this table.]
Status
Category
Lead
region
Priority
Scientific name
Family
Common name
Lexingtonia
dolabelloides.
Pleurobema
strodeanum.
Fusconaia escambia ..
Fusconaia
(=Quincuncina)
burkei.
Quadrula cylindrica
cylindrica.
Unionidae ...................
Unionidae ...................
Pearlymussel,
slabside.
Pigtoe, fuzzy ..............
U.S.A. (AL, KY, TN,
VA).
U.S.A. (AL, FL).
Unionidae ...................
Unionidae ...................
Pigtoe, narrow ............
Pigtoe, tapered ..........
U.S.A. (AL, FL).
U.S.A. (AL, FL).
Unionidae ...................
Rabbitsfoot .................
Unionidae ...................
Sandshell, southern ...
U.S.A. (AL, AR, GA,
IN, IL, KS, KY, LA,
MS, MO, OK, OH,
PA, TN, WV).
U.S.A. (AL, FL).
Unionidae ...................
Snuffbox .....................
C* ......................
2
R4
C .......................
5
R4
C .......................
C .......................
5
11
R4
R4
C .......................
9
R4
C .......................
5
R4
PE .....................
–
R3
C .......................
4
R3
Cumberlandia
monodonta.
Margaritiferidae ..........
Spectaclecase ............
PE .....................
2
R4
Elliptio spinosa ...........
Unionidae ...................
Spinymussel, Altamaha.
SNAILS:
C .......................
C* ......................
C* ......................
8
2
2
R4
R1
R2
Pleuroceridae .............
Potaridae ....................
Hydrobiidae ................
......................
......................
......................
......................
......................
......................
......................
......................
......................
......................
2
2
2
2
2
2
2
2
2
2
R1
R1
R1
R1
R1
R1
R2
R1
R1
R2
C* ......................
11
R8
Elimia melanoides ......
Ostodes strigatus .......
Pseudotryonia
adamantina.
Samoana fragilis ........
Partula radiolata .........
Partula gibba ..............
Partulina semicarinata
Partulina variabilis ......
Partula langfordi .........
Cochliopa texana .......
Newcombia cumingi ...
Eua zebrina ................
Pyrgulopsis
chupaderae.
Pyrgulopsis notidicola
C* ......................
C* ......................
11
2
R2
R2
Mudalia, black ............
Sisi snail .....................
Snail, Diamond Y
Spring.
Snail, fragile tree ........
Snail, Guam tree ........
Snail, Humped tree ....
Snail, Lanai tree .........
Snail, Lanai tree .........
Snail, Langford’s tree
Snail, Phantom cave ..
Snail, Newcomb’s tree
Snail, Tutuila tree .......
Springsnail,
Chupadera.
Springsnail, elongate
mud meadows.
Springsnail, Gila .........
Springsnail, Gonzales
C* ......................
C* ......................
8
11
C* ......................
C* ......................
C*
C*
C*
C*
C*
C*
C*
C*
C*
C*
Hamiota (=Lampsilis)
australis.
Epioblasma triquetra ..
Partulidae ...................
Partulidae ...................
Partulidae ...................
Achatinellidae .............
Achatinellidae .............
Partulidae ...................
Hydrobiidae ................
Achatinellidae .............
Partulidae ...................
Hydrobiidae ................
Hydrobiidae ................
8
2
R2
R2
Pyrgulopsis morrisoni
Tryonia cheatumi .......
Hydrobiidae ................
Hydrobiidae ................
C .......................
2
R2
2
R2
Pyrgulopsis
bernardina.
Pyrgulopsis trivialis ....
Hydrobiidae ................
C* ......................
C* ......................
5
R2
Sonorella
rosemontensis.
Helminthoglyptidae ....
INSECTS:
C* ......................
C .......................
jlentini on DSKJ8SOYB1PROD with PROPOSALS3
Hydrobiidae ................
Hydrobiidae ................
R2
R2
Pyrgulopsis gilae ........
Tryonia circumstriata
(=stocktonensis).
Pyrgulopsis thompsoni
Pyrgulopsis thermalis
8
3
R1
R4
Nysius wekiuicola ......
Strymon acis bartrami
Lygaeidae ..................
Lycaenidae .................
C .......................
3
R4
Nymphalidae ..............
C* ......................
3
R1
C* ......................
2
R1
Anaea troglodyta
floridalis.
Hypolimnas octucula
mariannensis.
Vagrans egistina ........
C* ......................
3
R4
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Jkt 223001
Cyclargus thomasi
bethunebakeri.
PO 00000
Frm 00068
Fmt 4701
Hydrobiidae ................
Hydrobiidae ................
Hydrobiidae ................
Nymphalidae ..............
Nymphalidae ..............
Lycaenidae .................
Sfmt 4702
Historical range
U.S.A. (IN, MI, NY,
OH, PA, WV), Canada (ON).
U.S.A. (AL, AR, IA,
IN, IL, KS, KY, MO,
MN, NE, OH, TN,
VA, WI, WV).
U.S.A. (GA).
U.S.A. (AL).
U.S.A. (AS).
U.S.A. (TX).
U.S.A.
U.S.A.
U.S.A.
U.S.A.
U.S.A.
U.S.A.
U.S.A.
U.S.A.
U.S.A.
U.S.A.
(GU, MP).
(GU).
(GU, MP).
(HI).
(HI).
(MP).
(TX).
(Hl).
(AS).
(NM).
U.S.A. (NV).
U.S.A. (NM).
U.S.A. (TX).
Springsnail, Huachuca
Springsnail, New Mexico.
Springsnail, Page .......
Springsnail (=Tryonia),
Phantom.
Springsnail, San
Bernardino.
Springsnail, Three
Forks.
Talussnail, Rosemont
U.S.A. (AZ), Mexico.
U.S.A. (NM).
Bug, Wekiu ................
Butterfly, Bartram’s
hairstreak.
Butterfly, Florida
leafwing.
Butterfly, Mariana
eight-spot.
Butterfly, Mariana
wandering.
Butterfly, Miami blue ..
U.S.A. (HI).
U.S.A. (FL).
E:\FR\FM\10NOP3.SGM
10NOP3
U.S.A. (AZ).
U.S.A. (TX).
U.S.A. (AZ), Mexico
(Sonora).
U.S.A. (AZ).
U.S.A. (AZ).
U.S.A. (FL).
U.S.A. (GU, MP).
U.S.A. (GU, MP).
U.S.A. (FL), Bahamas.
Federal Register / Vol. 75, No. 217 / Wednesday, November 10, 2010 / Proposed Rules
69289
TABLE 1—CANDIDATE NOTICE OF REVIEW (ANIMALS AND PLANTS)—Continued
[Note: See end of SUPPLEMENTARY INFORMATION for an explanation of symbols used in this table.]
Status
Category
Lead
region
Priority
Scientific name
Family
Common name
Historical range
Glyphopsyche
sequatchie.
Pseudanophthalmus
insularis.
Pseudanophthalmus
caecus.
Pseudanophthalmus
colemanensis.
Pseudanophthalmus
fowlerae.
Pseudanophthalmus
frigidus.
Pseudanophthalmus
tiresias.
Limnephilidae .............
Caddisfly, Sequatchie
U.S.A. (TN).
Carabidae ..................
U.S.A. (TN).
Carabidae ..................
Cave beetle, Baker
Station (= insular).
Cave beetle, Clifton ...
U.S.A. (KY).
Carabidae ..................
Cave beetle, Coleman
U.S.A. (TN).
Carabidae ..................
Cave beetle, Fowler’s
U.S.A. (TN).
Carabidae ..................
Cave beetle, icebox ...
U.S.A. (KY).
Carabidae ..................
U.S.A. (TN).
Pseudanophthalmus
inquisitor.
Pseudanophthalmus
troglodytes.
Pseudanophthalmus
paulus.
Pseudanophthalmus
parvus.
Euphydryas editha
taylori.
Megalagrion
nigrohamatum
nigrolineatum.
Megalagrion
leptodemas.
Megalagrion
oceanicum.
Megalagrion
xanthomelas.
Carabidae ..................
Cave beetle, Indian
Grave Point (=
Soothsayer).
Cave beetle, inquirer
U.S.A. (TN).
Carabidae ..................
Cave beetle, Louisville
U.S.A. (KY).
Carabidae ..................
Cave beetle, Noblett’s
U.S.A. (TN).
Carabidae ..................
Cave beetle, Tatum ...
U.S.A. (KY).
Nymphalidae ..............
Checkerspot butterfly,
Taylor’s (= Whulge).
Damselfly, blackline
Hawaiian.
U.S.A. (OR, WA),
Canada (BC).
U.S.A. (HI).
Damselfly, crimson
Hawaiian.
Damselfly, oceanic
Hawaiian.
Damselfly,
orangeblack Hawaiian.
June beetle, Casey’s
Naucorid bug
(=Furnace Creek),
Nevares Spring.
fly, Hawaiian Picturewing.
Riffle beetle,
Stephan’s.
Skipper, Dakota .........
U.S.A. (HI).
5
R4
C .......................
5
R4
C* ......................
5
R4
C .......................
11
R4
C .......................
5
R4
C* ......................
5
R4
C .......................
5
R4
C* ......................
5
R4
C* ......................
5
R4
C .......................
5
R4
C* ......................
5
R4
C* ......................
3
R1
C* ......................
9
R1
C* ......................
2
R1
C* ......................
2
R1
C* ......................
8
R1
PE .....................
C .......................
2
5
R8
R8
Dinacoma caseyi .......
Ambrysus funebris .....
Scarabidae .................
Naucoridae .................
C* ......................
2
R1
Drosophila digressa ...
Drosophilidae .............
C* ......................
8
R2
Heterelmis stephani ...
Elmidae ......................
C* ......................
8
R3
Hesperia dacotae .......
Hesperiidae ................
C* ......................
C* ......................
8
2
R1
R6
Polites mardon ...........
Cicindela albissima ....
Hesperiidae ................
Cicindelidae ...............
C* ......................
5
R4
Cicindela
highlandensis.
Cicindelidae ...............
ARACHNIDS:
C* ......................
2
R2
Cicurina wartoni .........
Dictynidae ..................
Meshweaver, Warton’s cave.
U.S.A. (TX).
CRUSTACEANS:
C .......................
2
R2
Amphipod, diminutive
U.S.A. (TX).
8
5
R5
R1
Gammarus
hyalleloides.
Stygobromus kenki ....
Metabetaeus lohena ..
Gammaridae ..............
C .......................
C* ......................
jlentini on DSKJ8SOYB1PROD with PROPOSALS3
C* ......................
Crangonyctidae ..........
Alpheidae ...................
U.S.A. (DC, MD).
U.S.A. (HI).
C* ......................
5
R1
Palaemonella burnsi ..
Palaemonidae ............
C* ......................
5
R1
Procaris hawaiana .....
Procarididae ...............
C* ......................
4
R1
Vetericaris chaceorum
Procaridae ..................
Amphipod, Kenk’s ......
Shrimp, anchialine
pool.
Shrimp, anchialine
pool.
Shrimp, anchialine
pool.
Shrimp, anchialine
pool.
FLOWERING
PLANTS:
C* ......................
11
R8
Abronia alpina ............
Nyctaginaceae ...........
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17:02 Nov 09, 2010
Jkt 223001
PO 00000
Frm 00069
Fmt 4701
Coenagrionidae ..........
Coenagrionidae ..........
Coenagrionidae ..........
Coenagrionidae ..........
Sfmt 4702
Skipper, Mardon ........
Tiger beetle, Coral
Pink Sand Dunes.
Tiger beetle, highlands.
U.S.A. (HI).
U.S.A. (HI).
U.S.A. (CA).
U.S.A. (CA).
U.S.A. (HI).
U.S.A. (AZ).
U.S.A. (MN, IA, SD,
ND, IL), Canada.
U.S.A. (CA, OR, WA).
U.S.A. (UT).
U.S.A. (FL).
U.S.A. (HI).
U.S.A. (HI).
U.S.A. (HI).
Sand-verbena,
U.S.A. (CA).
Ramshaw Meadows.
E:\FR\FM\10NOP3.SGM
10NOP3
69290
Federal Register / Vol. 75, No. 217 / Wednesday, November 10, 2010 / Proposed Rules
TABLE 1—CANDIDATE NOTICE OF REVIEW (ANIMALS AND PLANTS)—Continued
[Note: See end of SUPPLEMENTARY INFORMATION for an explanation of symbols used in this table.]
Status
Category
Scientific name
Family
Common name
Agave eggersiana ......
Arabis georgiana ........
Argythamnia blodgettii
Artemisia campestris
var. wormskioldii.
Astragalus anserinus
Agavaceae .................
Brassicaceae .............
Euphorbiaceae ...........
Asteraceae .................
No common name .....
Rockcress, Georgia ...
Silverbush, Blodgett’s
Wormwood, northern
U.S.A.
U.S.A.
U.S.A.
U.S.A.
Fabaceae ...................
U.S.A. (ID, NV, UT).
Astragalus cusickii
var. packardiae.
Astragalus tortipes .....
Fabaceae ...................
Milkvetch, Goose
Creek.
Milkvetch, Packard’s ..
......................
......................
......................
......................
8
8
11
3
R4
R4
R4
R1
C* ......................
5
R1
C .......................
3
R1
C* ......................
11
R6
C* ......................
C* ......................
2
3
R1
R1
C* ......................
3
R1
C* ......................
C* ......................
8
3
R1
R1
C* ......................
C* ......................
8
2
R4
R1
C* ......................
2
R1
C* ......................
5
R8
C* ......................
C* ......................
C* ......................
2
8
9
R1
R1
R4
C* ......................
12
R4
C* ......................
9
R4
C* ......................
6
R8
C* ......................
2
R4
Bidens amplectens ....
Bidens campylotheca
pentamera.
Bidens campylotheca
waihoiensis.
Bidens conjuncta .......
Bidens micrantha
ctenophylla.
Brickellia mosieri ........
Calamagrostis
expansa.
Calamagrostis
hillebrandii.
Calochortus
persistens.
Canavalia pubescens
Castilleja christii .........
Chamaecrista lineata
var. keyensis.
Chamaesyce
deltoidea pinetorum.
Chamaesyce
deltoidea serpyllum.
Chorizanthe parryi
var. fernandina.
Chromolaena frustrata
C* ......................
2
R4
Consolea corallicola ...
Cactaceae ..................
C*
C*
C*
C*
C*
C*
C*
C*
C*
C*
C*
C*
......................
......................
......................
......................
......................
......................
......................
......................
......................
......................
......................
......................
5
2
2
2
2
2
2
2
2
2
2
3
R4
R1
R1
R1
R1
R1
R1
R1
R1
R1
R1
R4
C* ......................
5
R5
Cordia rupicola ...........
Cyanea asplenifolia ...
Cyanea calycina ........
Cyanea kunthiana ......
Cyanea lanceolata .....
Cyanea obtusa ...........
Cyanea tritomantha ...
Cyrtandra filipes .........
Cyrtandra kaulantha ..
Cyrtandra oxybapha ..
Cyrtandra sessilis ......
Dalea carthagenensis
var. floridana.
Dichanthelium hirstii ...
C* ......................
5
R4
C* ......................
jlentini on DSKJ8SOYB1PROD with PROPOSALS3
C*
C*
C*
C*
Lead
region
Priority
3
R2
C* ......................
C* ......................
8
2
R2
R1
C* ......................
6
R8
C .......................
5
R8
VerDate Mar<15>2010
17:02 Nov 09, 2010
Jkt 223001
Fabaceae ...................
Historical range
(VI).
(AL, GA).
(FL).
(OR, WA).
U.S.A. (ID).
Asteraceae .................
Asteraceae .................
Milkvetch, Sleeping
Ute.
Ko‘oko‘olau ................
Ko‘oko‘olau ................
U.S.A. (HI).
U.S.A. (HI).
Asteraceae .................
Ko‘oko‘olau ................
U.S.A. (HI).
Asteraceae .................
Asteraceae .................
Ko‘oko‘olau ................
Ko‘oko‘olau ................
U.S.A. (HI).
U.S.A. (HI).
Asteraceae .................
Poaceae .....................
Brickell-bush, Florida
Reedgrass, Maui ........
U.S.A. (FL).
U.S.A. (HI).
Poaceae .....................
Reedgrass,
Hillebrand’s.
Mariposa lily, Siskiyou
U.S.A. (HI).
Liliaceae .....................
U.S.A. (CA, OR).
U.S.A. (HI).
U.S.A. (ID).
U.S.A. (FL).
Euphorbiaceae ...........
‘Awikiwiki ....................
Paintbrush, Christ’s ....
Pea, Big Pine partridge.
Sandmat, pineland .....
Euphorbiaceae ...........
Spurge, wedge ...........
U.S.A. (FL).
Polygonaceae ............
U.S.A. (CA).
Boraginaceae .............
Campanulaceae .........
Campanulaceae .........
Campanulaceae .........
Campanulaceae .........
Campanulaceae .........
Campanulaceae .........
Gesneriaceae .............
Gesneriaceae .............
Gesneriaceae .............
Gesneriaceae .............
Fabaceae ...................
Spineflower, San Fernando Valley.
Thoroughwort, Cape
Sable.
Cactus, Florida semaphore.
No common name .....
Haha ..........................
Haha ..........................
Haha ..........................
Haha ..........................
Haha ..........................
‘Aku ............................
Ha‘iwale .....................
Ha‘iwale .....................
Ha‘iwale .....................
Ha‘iwale .....................
Prairie-clover, Florida
Poaceae .....................
Panic grass, Hirsts’ ....
Digitaria pauciflora .....
Poaceae .....................
Echinomastus
erectocentrus var.
acunensis.
Erigeron lemmonii ......
Eriogonum codium .....
Cactaceae ..................
Crabgrass, Florida
pineland.
Cactus, Acuna ...........
Eriogonum
corymbosum var.
nilesii.
Eriogonum
diatomaceum.
PO 00000
Frm 00070
Fmt 4701
Fabaceae ...................
Scrophulariaceae .......
Fabaceae ...................
U.S.A. (CO).
Asteraceae .................
Asteraceae .................
Polygonaceae ............
Polygonaceae ............
Polygonaceae ............
Sfmt 4702
U.S.A. (FL).
U.S.A. (FL).
U.S.A. (FL).
U.S.A.
U.S.A.
U.S.A.
U.S.A.
U.S.A.
U.S.A.
U.S.A.
U.S.A.
U.S.A.
U.S.A.
U.S.A.
U.S.A.
(PR), Anegada.
(HI).
(HI).
(HI).
(HI).
(HI).
(HI).
(HI).
(HI).
(HI).
(HI).
(FL).
U.S.A. (DE, GA, NC,
NJ).
U.S.A. (FL).
U.S.A. (AZ), Mexico.
Fleabane, Lemmon ....
Buckwheat, Umtanum
Desert.
Buckwheat, Las
Vegas.
U.S.A. (AZ).
U.S.A. (WA).
Buckwheat, Churchill
Narrows.
U.S.A. (NV).
E:\FR\FM\10NOP3.SGM
10NOP3
U.S.A. (NV).
69291
Federal Register / Vol. 75, No. 217 / Wednesday, November 10, 2010 / Proposed Rules
TABLE 1—CANDIDATE NOTICE OF REVIEW (ANIMALS AND PLANTS)—Continued
[Note: See end of SUPPLEMENTARY INFORMATION for an explanation of symbols used in this table.]
Status
Category
Lead
region
Priority
Scientific name
Family
Common name
Historical range
C* ......................
5
R8
Eriogonum kelloggii ...
Polygonaceae ............
C* ......................
C* ......................
C* ......................
C* ......................
C* ......................
C* ......................
C .......................
2
11
2
8
8
5
2
R1
R2
R1
R1
R1
R4
R4
Festuca hawaiiensis ..
Festuca ligulata ..........
Gardenia remyi ..........
Geranium hanaense ..
Geranium hillebrandii
Gonocalyx concolor ...
Harrisia aboriginum ....
Poaceae .....................
Poaceae .....................
Rubiaceae ..................
Geraniaceae ..............
Geraniaceae ..............
Ericaceae ...................
Cactaceae ..................
......................
......................
......................
......................
5
2
8
2
R8
R1
R4
R2
Hazardia orcuttii .........
Hedyotis fluviatilis ......
Helianthus verticillatus
Hibiscus dasycalyx ....
Asteraceae .................
Rubiaceae ..................
Asteraceae .................
Malvaceae ..................
PE .....................
C* ......................
C* ......................
2
5
3
R6
R8
R1
Polemoniaceae ..........
Rosaceae ...................
Joinvilleaceae ............
C* ......................
C* ......................
C .......................
2
5
3
R1
R4
R4
Viscaceae ..................
Brassicaceae .............
Brassicaceae .............
Hulumoa .....................
Gladecress, unnamed
Gladecress, Kentucky
U.S.A. (HI).
U.S.A. (AL).
U.S.A. (KY).
C* ......................
2
R2
Ipomopsis polyantha ..
Ivesia webberi ............
Joinvillea ascendens
ascendens.
Korthalsella degeneri
Leavenworthia crassa
Leavenworthia exigua
var. laciniata.
Leavenworthia texana
Buckwheat, Red
Mountain.
No common name .....
Fescue, Guadalupe ...
Nanu ..........................
Nohoanu ....................
Nohoanu ....................
No common name .....
Pricklyapple, aboriginal (shellmound
applecactus).
Orcutt’s hazardia ........
Kampua‘a ...................
Sunflower, whorled ....
Rose-mallow, Neches
River.
Skyrocket, Pagosa .....
Ivesia, Webber ...........
‘Ohe ...........................
Brassicaceae .............
U.S.A. (TX).
C* ......................
C* ......................
C* ......................
8
5
3
R4
R4
R4
Brassicaceae .............
Linaceae ....................
Linaceae ....................
C* ......................
2
R1
C* ......................
C* ......................
C .......................
2
2
3
R1
R1
R8
C* ......................
C* ......................
C* ......................
2
2
8
R1
R1
R5
C* ......................
2
R1
C* ......................
C* ......................
2
3
R1
R2
PT .....................
2
R6
Lesquerella globosa ...
Linum arenicola .........
Linum carteri var.
carteri.
Melicope
christophersenii.
Melicope hiiakae ........
Melicope makahae .....
Mimulus fremontii var.
vandenbergensis.
Myrsine fosbergii ........
Myrsine vaccinioides ..
Narthecium
americanum.
Nothocestrum
latifolium.
Ochrosia haleakalae ..
Pediocactus
peeblesianus var.
fickeiseniae.
Penstemon debilis .....
Gladecress, Texas
golden.
Bladderpod, Short’s ...
Flax, sand ..................
Flax, Carter’s smallflowered.
Alani ...........................
C* ......................
9
R6
Scrophulariaceae .......
C* ......................
2
R1
C .......................
PT .....................
C* ......................
C* ......................
C* ......................
5
8
2
8
9
R8
R6
R1
R1
R1
C* ......................
8
R4
Penstemon scariosus
var. albifluvis.
Peperomia
subpetiolata.
Phacelia stellaris ........
Phacelia submutica ....
Phyllostegia bracteata
Phyllostegia floribunda
Physaria douglasii
tuplashensis.
Platanthera
integrilabia.
C* ......................
3
R1
C* ......................
3
R1
C* ......................
C .......................
C* ......................
2
2
2
R1
R1
R1
jlentini on DSKJ8SOYB1PROD with PROPOSALS3
C*
C*
C*
C*
VerDate Mar<15>2010
17:02 Nov 09, 2010
Jkt 223001
Platydesma cornuta
var. cornuta.
Platydesma cornuta
var. decurrens.
Platydesma remyi ......
Pleomele fernaldii ......
Pleomele forbesii .......
PO 00000
Frm 00071
Fmt 4701
Rutaceae ....................
Rutaceae ....................
Rutaceae ....................
Phrymaceae ...............
U.S.A. (CA).
U.S.A.
U.S.A.
U.S.A.
U.S.A.
U.S.A.
U.S.A.
U.S.A.
(HI).
(TX), Mexico.
(HI).
(HI).
(HI).
(PR).
(FL).
U.S.A.
U.S.A.
U.S.A.
U.S.A.
(CA), Mexico.
(HI).
(AL, GA, TN).
(TX).
U.S.A. (CO).
U.S.A. (CA, NV).
U.S.A. (HI).
U.S.A. (IN, KY, TN).
U.S.A. (FL).
U.S.A. (FL).
U.S.A. (HI).
Myrsinaceae ...............
Myrsinaceae ...............
Liliaceae .....................
Alani ...........................
Alani ...........................
Monkeyflower, Vandenberg.
Kolea ..........................
Kolea ..........................
Asphodel, bog ............
Solanaceae ................
‘Aiea ...........................
Apocynaceae .............
Cactaceae ..................
Holei ...........................
Cactus, Fickeisen
plains.
U.S.A. (HI).
U.S.A. (AZ).
Scrophulariaceae .......
Beardtongue, Parachute.
Beardtongue, White
River.
‘Ala ‘ala wai nui ..........
U.S.A. (CO).
Piperaceae .................
Hydrophyllaceae ........
Hydrophyllaceae ........
Lamiaceae .................
Lamiaceae .................
Brassicaceae .............
Orchidaceae ...............
Phacelia, Brand’s .......
Phacelia, DeBeque ....
No common name .....
No common name .....
Bladderpod, White
Bluffs.
Orchid, white
fringeless.
U.S.A. (HI).
U.S.A. (HI).
U.S.A. (CA).
U.S.A. (HI).
U.S.A. (HI).
U.S.A. (DE, NC, NJ,
NY, SC).
U.S.A. (HI).
U.S.A. (CO, UT).
U.S.A. (HI).
U.S.A.
U.S.A.
U.S.A.
U.S.A.
U.S.A.
(CA), Mexico.
(CO).
(HI).
(HI).
(WA).
Rutaceae ....................
No common name .....
U.S.A. (AL, GA, KY,
MS, NC, SC, TN,
VA).
U.S.A. (HI).
Rutaceae ....................
No common name .....
U.S.A. (HI).
Rutaceae ....................
Agavaceae .................
Agavaceae .................
No common name .....
Hala pepe ..................
Hala pepe ..................
U.S.A. (HI).
U.S.A. (HI).
U.S.A. (HI).
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TABLE 1—CANDIDATE NOTICE OF REVIEW (ANIMALS AND PLANTS)—Continued
[Note: See end of SUPPLEMENTARY INFORMATION for an explanation of symbols used in this table.]
Status
Category
Lead
region
Priority
Scientific name
Family
Common name
Historical range
U.S.A. (HI).
C* ......................
11
R8
Potentilla basaltica .....
Rosaceae ...................
C* ......................
3
R1
Asteraceae .................
C* ......................
3
R1
Rubiaceae ..................
Kopiko ........................
U.S.A. (HI).
C* ......................
C* ......................
2
2
R1
R1
Apocynaceae .............
Ranunculaceae ..........
Kaulu ..........................
Makou ........................
U.S.A. (HI).
U.S.A. (HI).
C*
C*
C*
C*
C*
......................
......................
......................
......................
......................
2
8
2
2
5
R1
R8
R1
R1
R8
Pseudognaphalium
(=Gnaphalium)
sandwicensium var.
molokaiense.
Psychotria hexandra
ssp. oahuensis var.
oahuensis.
Pteralyxia macrocarpa
Ranunculus
hawaiensis.
Ranunculus mauiensis
Rorippa subumbellata
Schiedea pubescens
Schiedea salicaria ......
Sedum eastwoodiae ..
Cinquefoil, Soldier
Meadow.
‘Ena‘ena .....................
Ranunculaceae ..........
Brassicaceae .............
Caryophyllaceae ........
Caryophyllaceae ........
Crassulaceae .............
U.S.A.
U.S.A.
U.S.A.
U.S.A.
U.S.A.
C* ......................
C .......................
2
12
R1
R4
Makou ........................
Cress, Tahoe yellow ..
Ma‘oli‘oli .....................
No common name .....
Stonecrop, Red Mountain.
‘Anunu ........................
Bully, Everglades .......
C* ......................
C .......................
8
8
R1
R4
C* ......................
C* ......................
C* ......................
2
2
8
R2
R1
R4
C* ......................
2
R1
FERNS AND
ALLIES:
C* ......................
8
R1
C* ......................
C* ......................
2
2
R1
R1
C* ......................
3
R1
C .......................
3
R4
Sicyos macrophyllus ..
Sideroxylon reclinatum
austrofloridense.
Solanum nelsonii .......
Solidago plumosa ......
Cucurbitaceae ............
Sapotaceae ................
Solanaceae ................
Asteraceae .................
U.S.A. (NV).
(HI).
(CA, NV).
(HI).
(HI).
(CA).
U.S.A. (HI).
U.S.A. (FL).
Sphaeralcea gierischii
Stenogyne cranwelliae
Symphyotrichum
georgianum.
Zanthoxylum
oahuense.
Malvaceae ..................
Lamiaceae .................
Asteraceae .................
Popolo ........................
Goldenrod, Yadkin
River.
Mallow, Gierisch ........
No common name .....
Aster, Georgia ............
U.S.A. (HI).
U.S.A. (NC).
Rutaceae ....................
A‘e ..............................
U.S.A. (AZ, UT).
U.S.A. (HI).
U.S.A. (AL, FL, GA,
NC, SC).
U.S.A. (HI).
Christella boydiae (=
Cyclosorus boydiae
var. boydiae +
Cyclosorus boydiae
kipahuluensis).
Doryopteris takeuchii
Huperzia (=
Phlegmariurus)
stemmermanniae.
Microlepia strigosa
var. mauiensis (=
Microlepia
mauiensis).
Trichomanes
punctatum
floridanum.
Thelypteridaceae .......
No common name .....
U.S.A. (HI).
Pteridaceae ................
Lycopodiaceae ...........
No common name .....
Wawae‘iole .................
U.S.A. (HI).
U.S.A. (HI).
Dennstaedtiaceae ......
Palapalai ....................
U.S.A. (HI).
Hymenophyllaceae ....
Florida bristle fern ......
U.S.A. (FL).
TABLE 2—ANIMALS AND PLANTS FORMERLY CANDIDATES OR FORMERLY PROPOSED FOR LISTING
[Note: See end of SUPPLEMENTARY INFORMATION for an explanation of symbols used in this table.]
Status
Code
Expl.
Lead
region
Scientific name
Family
Common name
Historical range
jlentini on DSKJ8SOYB1PROD with PROPOSALS3
MAMMALS:
Rc .....................
A, U
R8
Xerospermophilus
tereticaudus chlorus.
Sciuridae ....................
Squirrel, Palm Springs
(= Coachella Valley)
round-tailed ground.
U.S.A. (CA).
BIRDS:
E .......................
L
R1
Loxops caeruleirostris
Fringillidae ..................
U.S.A. (HI).
L
R1
Oreomystis bairdi .......
Fringillidae ..................
Akekee
(honeycreeper).
Akikiki (Kauai creeper)
U.S.A. (HI).
L
R4
Pleurobema
hanleyianum.
Unionidae ...................
Pigtoe, Georgia ..........
U.S.A. (AL, GA, TN).
E .......................
CLAMS:
E .......................
SNAILS:
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TABLE 2—ANIMALS AND PLANTS FORMERLY CANDIDATES OR FORMERLY PROPOSED FOR LISTING—Continued
[Note: See end of SUPPLEMENTARY INFORMATION for an explanation of symbols used in this table.]
Status
Code
Expl.
Lead
region
Scientific name
Family
Common name
Historical range
L
L
R4
R4
Pleurocera foremani ...
Leptoxis foremani (=
downei).
Pleuroceridae .............
Pleuroceridae .............
Hornsnail, rough .........
Rocksnail, Interrupted
(= Georgia).
U.S.A. (AL).
U.S.A. (GA, AL).
INSECTS:
E .......................
L
R1
Megalagrion nesiotes
Coenagrionidae ..........
L
R1
Megalagrion pacificum
Coenagrionidae ..........
E .......................
L
R1
Drosophila attigua ......
Drosophilidae .............
Damselfly, flying
earwig Hawaiian.
Damselfly, Pacific Hawaiian.
Fly, Hawaiian picturewing.
U.S.A. (HI).
E .......................
FLOWERING
PLANTS:
E .......................
E .......................
E .......................
L
L
L
R1
R1
R1
Pa‘iniu .........................
‘Awikiwiki ....................
‘Akoko .........................
U.S.A. (HI).
U.S.A. (HI).
U.S.A. (HI).
L
R1
Euphorbiaceae ...........
‘Akoko .........................
U.S.A. (HI).
E .......................
L
R1
Euphorbiaceae ...........
‘Akoko .........................
U.S.A. (HI).
E .......................
L
R1
Amaranthaceae ..........
Papala ........................
U.S.A. (HI).
E
E
E
E
E
E
E
.......................
.......................
.......................
.......................
.......................
.......................
.......................
L
L
L
L
L
L
L
R1
R1
R1
R1
R1
R1
R1
Campanulaceae .........
Campanulaceae .........
Campanulaceae .........
Campanulaceae .........
Gesneriaceae .............
Gesneriaceae .............
Asteraceae .................
Haha ...........................
Haha ...........................
Haha ...........................
Haha ...........................
Ha‘iwale ......................
Ha‘iwale ......................
Na‘ena‘e .....................
U.S.A.
U.S.A.
U.S.A.
U.S.A.
U.S.A.
U.S.A.
U.S.A.
E .......................
E .......................
E .......................
L
L
L
R1
R1
R1
Asteraceae .................
Asteraceae .................
Asteraceae .................
Na‘ena‘e .....................
Na‘ena‘e .....................
Na‘ena‘e .....................
U.S.A. (HI).
U.S.A. (HI).
U.S.A. (HI).
E
E
E
E
E
E
T
E
.......................
.......................
.......................
.......................
.......................
.......................
.......................
.......................
L
L
L
L
L
L
L
L
R1
R1
R1
R1
R1
R1
R1
R1
Asteraceae .................
Geraniaceae ...............
Asteraceae .................
Asteraceae .................
Loganiaceae ...............
Loganiaceae ...............
Brassicaceae ..............
Myrsinaceae ...............
Na‘ena‘e .....................
Nohoanu .....................
No common name ......
No common name ......
Kamakahala ...............
Kamakahala ...............
Peppergrass, slickspot
Lehua makanoe .........
U.S.A.
U.S.A.
U.S.A.
U.S.A.
U.S.A.
U.S.A.
U.S.A.
U.S.A.
E .......................
E .......................
E .......................
L
L
L
R1
R1
R1
Myrsinaceae ...............
Myrsinaceae ...............
Myrsinaceae ...............
No common name ......
No common name ......
No common name ......
U.S.A. (HI).
U.S.A. (HI).
U.S.A. (HI).
E
E
E
E
E
E
E
E
.......................
.......................
.......................
.......................
.......................
.......................
.......................
.......................
L
L
L
L
L
L
L
L
R1
R1
R1
R1
R1
R1
R1
R1
Myrsinaceae ...............
Rutaceae ....................
Rutaceae ....................
Rutaceae ....................
Myrsinaceae ...............
Myrsinaceae ...............
Lamiaceae ..................
Pittosporaceae ...........
No common name ......
Alani ...........................
Alani ...........................
Alani ...........................
Kolea ..........................
Kolea ..........................
No common name ......
Ho‘awa .......................
U.S.A.
U.S.A.
U.S.A.
U.S.A.
U.S.A.
U.S.A.
U.S.A.
U.S.A.
(HI).
(HI).
(HI).
(HI).
(HI).
(HI).
(HI).
(HI).
E
E
E
E
E
E
E
.......................
.......................
.......................
.......................
.......................
.......................
.......................
L
L
L
L
L
L
L
R1
R1
R1
R1
R1
R1
R1
Rutaceae ....................
Asteraceae .................
Rubiaceae ..................
Rubiaceae ..................
Caryophyllaceae .........
Lamiaceae ..................
Araliaceae ..................
Pilo kea lau li‘i ............
Lo‘ulu ..........................
Kopiko ........................
Kopiko ........................
No common name ......
No common name ......
No common name ......
U.S.A.
U.S.A.
U.S.A.
U.S.A.
U.S.A.
U.S.A.
U.S.A.
(HI).
(HI).
(HI).
(HI).
(HI).
(HI).
(HI).
E .......................
E .......................
E .......................
L
L
L
R1
R1
R1
Astelia waialealae ......
Canavalia napaliensis
Chamaesyce
eleanoriae.
Chamaesyce remyi
var. kauaiensis.
Chamaesyce remyi
var. remyi.
Charpentiera
densiflora.
Cyanea dolichopoda ..
Cyanea eleeleensis ....
Cyanea kolekoleensis
Cyanea kuhihewa .......
Cyrtandra oenobarba
Cyrtandra paliku .........
Dubautia imbricata
imbricata.
Dubautia kalalauensis
Dubautia kenwoodii ....
Dubautia plantaginea
magnifolia.
Dubautia waialealae ...
Geranium kauaiense ..
Keysseria erici ............
Keysseria helenae ......
Labordia helleri ...........
Labordia pumila ..........
Lepidium papilliferum
Lysimachia
daphnoides.
Lysimachia iniki ..........
Lysimachia pendens ..
Lysimachia
scopulensis.
Lysimachia venosa .....
Melicope degeneri ......
Melicope paniculata ...
Melicope puberula ......
Myrsine knudsenii ......
Myrsine mezii .............
Phyllostegia renovans
Pittosporum
napaliense.
Platydesma rostrata ...
Pritchardia hardyi .......
Psychotria grandiflora
Psychotria hobdyi .......
Schiedea attenuata ....
Stenogyne kealiae ......
Tetraplasandra
bisattenuata.
Tetraplasandra flynnii
Diellia mannii ..............
Doryopteris angelica ..
Liliaceae .....................
Fabaceae ...................
Euphorbiaceae ...........
E .......................
jlentini on DSKJ8SOYB1PROD with PROPOSALS3
E .......................
E .......................
Araliaceae ..................
Aspleniaceae ..............
Pteridaceae ................
No common name ......
No common name ......
No common name ......
U.S.A. (HI).
U.S.A. (HI).
U.S.A. (HI).
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U.S.A. (HI).
U.S.A. (HI).
(HI).
(HI).
(HI).
(HI).
(HI).
(HI).
(HI).
(HI).
(HI).
(HI).
(HI).
(HI).
(HI).
(ID).
(HI).
69294
Federal Register / Vol. 75, No. 217 / Wednesday, November 10, 2010 / Proposed Rules
TABLE 2—ANIMALS AND PLANTS FORMERLY CANDIDATES OR FORMERLY PROPOSED FOR LISTING—Continued
[Note: See end of SUPPLEMENTARY INFORMATION for an explanation of symbols used in this table.]
Status
Code
Expl.
E .......................
L
Lead
region
R1
Scientific name
Family
Common name
Dryopteris crinalis var.
podosorus.
Dryopteridaceae .........
Palapalai aumakua .....
[FR Doc. 2010–27686 Filed 11–9–10; 8:45 am]
jlentini on DSKJ8SOYB1PROD with PROPOSALS3
BILLING CODE P
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Historical range
U.S.A. (HI).
Agencies
[Federal Register Volume 75, Number 217 (Wednesday, November 10, 2010)]
[Proposed Rules]
[Pages 69222-69294]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2010-27686]
[[Page 69221]]
-----------------------------------------------------------------------
Part III
Department of the Interior
-----------------------------------------------------------------------
Fish and Wildlife Service
-----------------------------------------------------------------------
50 CFR Part 17
Endangered and Threatened Wildlife and Plants; Review of Native Species
That Are Candidates for Listing as Endangered or Threatened; Annual
Notice of Findings on Resubmitted Petitions; Annual Description of
Progress on Listing Actions; Proposed Rule
Federal Register / Vol. 75 , No. 217 / Wednesday, November 10, 2010 /
Proposed Rules
[[Page 69222]]
-----------------------------------------------------------------------
DEPARTMENT OF THE INTERIOR
Fish and Wildlife Service
50 CFR Part 17
[Docket No. FWS-R9-ES-2010-0065; MO-9221050083-B2]
Endangered and Threatened Wildlife and Plants; Review of Native
Species That Are Candidates for Listing as Endangered or Threatened;
Annual Notice of Findings on Resubmitted Petitions; Annual Description
of Progress on Listing Actions
AGENCY: Fish and Wildlife Service, Interior.
ACTION: Notice of review.
-----------------------------------------------------------------------
SUMMARY: In this Candidate Notice of Review (CNOR), we, the U.S. Fish
and Wildlife Service (Service), present an updated list of plant and
animal species native to the United States that we regard as candidates
for or have proposed for addition to the Lists of Endangered and
Threatened Wildlife and Plants under the Endangered Species Act of
1973, as amended. Identification of candidate species can assist
environmental planning efforts by providing advance notice of potential
listings, allowing landowners and resource managers to alleviate
threats and thereby possibly remove the need to list species as
endangered or threatened. Even if we subsequently list a candidate
species, the early notice provided here could result in more options
for species management and recovery by prompting candidate conservation
measures to alleviate threats to the species.
The CNOR summarizes the status and threats that we evaluated in
order to determine that species qualify as candidates and to assign a
listing priority number (LPN) to each species or to determine that
species should be removed from candidate status. Additional material
that we relied on is available in the Species Assessment and Listing
Priority Assignment Forms (species assessment forms, previously called
candidate forms) for each candidate species.
Overall, this CNOR recognizes five new candidates, changes the LPN
for four candidates, and removes one species from candidate status.
Combined with other decisions for individual species that were
published separately from this CNOR in the past year, the current
number of species that are candidates for listing is 251.
This document also includes our findings on resubmitted petitions
and describes our progress in revising the Lists of Endangered and
Threatened Wildlife and Plants during the period October 1, 2009,
through September 30, 2010.
We request additional status information that may be available for
the 251 candidate species identified in this CNOR.
DATES: We will accept information on any of the species in this
Candidate Notice of Review at any time.
ADDRESSES: This notice is available on the Internet at https://www.regulations.gov and https://www.fws.gov/endangered/what-we-do/cnor.html. Species assessment forms with information and references on
a particular candidate species' range, status, habitat needs, and
listing priority assignment are available for review at the appropriate
Regional Office listed below in SUPPLEMENTARY INFORMATION or at the
Branch of Candidate Conservation, Arlington, VA (see address below), or
on our Web site (https://ecos.fws.gov/tess_public/pub/SpeciesReport.do?listingType=C&mapstatus=1). Please submit any new
information, materials, comments, or questions of a general nature on
this notice to the Arlington, VA, address listed below. Please submit
any new information, materials, comments, or questions pertaining to a
particular species to the address of the Endangered Species Coordinator
in the appropriate Regional Office listed in SUPPLEMENTARY INFORMATION.
FOR FURTHER INFORMATION CONTACT: The Endangered Species Coordinator(s)
in the appropriate Regional Office(s), or Chief, Branch of Candidate
Conservation, U.S. Fish and Wildlife Service, 4401 N. Fairfax Drive,
Room 420, Arlington, VA 22203 (telephone 703-358-2171; facsimile 703-
358-1735). Persons who use a telecommunications device for the deaf
(TDD) may call the Federal Information Relay Service (FIRS) at 800-877-
8339.
SUPPLEMENTARY INFORMATION: We request additional status information
that may be available for any of the candidate species identified in
this CNOR. We will consider this information to monitor changes in the
status or LPN of candidate species and to manage candidates as we
prepare listing documents and future revisions to the notice of review.
We also request information on additional species to consider including
as candidates as we prepare future updates of this notice.
You may submit your information concerning this notice in general
or for any of the species included in this notice by one of the methods
listed in the ADDRESSES section.
Species-specific information and materials we receive will be
available for public inspection by appointment, during normal business
hours, at the appropriate Regional Office listed below under Request
for Information in SUPPLEMENTARY INFORMATION. General information we
receive will be available at the Branch of Candidate Conservation,
Arlington, VA (see address above).
Candidate Notice of Review
Background
The Endangered Species Act of 1973, as amended (16 U.S.C. 1531 et
seq.) (Act), requires that we identify species of wildlife and plants
that are endangered or threatened, based on the best available
scientific and commercial information. As defined in section 3 of the
Act, an endangered species is any species which is in danger of
extinction throughout all or a significant portion of its range, and a
threatened species is any species which is likely to become an
endangered species within the foreseeable future throughout all or a
significant portion of its range. Through the Federal rulemaking
process, we add species that meet these definitions to the List of
Endangered and Threatened Wildlife at 50 CFR 17.11 or the List of
Endangered and Threatened Plants at 50 CFR 17.12. As part of this
program, we maintain a list of species that we regard as candidates for
listing. A candidate species is one for which we have on file
sufficient information on biological vulnerability and threats to
support a proposal to list as endangered or threatened, but for which
preparation and publication of a proposal is precluded by higher
priority listing actions. We may identify a species as a candidate for
listing after we have conducted an evaluation of its status on our own
initiative, or after we have made a positive finding on a petition to
list a species, in particular we have found that listing is warranted
but precluded by other higher priority listing action (see the Petition
Findings section, below).
We maintain this list of candidates for a variety of reasons: To
notify the public that these species are facing threats to their
survival; to provide advance knowledge of potential listings that could
affect decisions of environmental planners and developers; to provide
information that may stimulate and guide conservation efforts that will
remove or reduce threats to these species and possibly make listing
unnecessary; to request input from interested parties to help us
identify those candidate species that may not
[[Page 69223]]
require protection under the Act or additional species that may require
the Act's protections; and to request necessary information for setting
priorities for preparing listing proposals. We strongly encourage
collaborative conservation efforts for candidate species, and offer
technical and financial assistance to facilitate such efforts. For
additional information regarding such assistance, please contact the
appropriate Regional Office listed under Request for Information or
visit our Web site, https://www.fws.gov/endangered/what-we-do/cca.html.
Previous Notices of Review
We have been publishing candidate notices of review (CNOR) since
1975. The most recent CNOR (prior to this CNOR) was published on
November 9, 2009 (74 FR 57804). CNORs published since 1994 are
available on our Web site, https://www.fws.gov/endangered/what-we-do/cnor.html. For copies of CNORs published prior to 1994, please contact
the Branch of Candidate Conservation (see ADDRESSES section above).
On September 21, 1983, we published 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, immediacy of threats, and taxonomic status; the lower the LPN,
the higher the listing priority (that is, a species with an LPN of 1
would have the highest listing priority). Section 4(h)(3) of the Act
(15 U.S.C. 1533(h)(3)) requires the Secretary to establish guidelines
for such a priority-ranking guidance system. As explained below, in
using this system we first categorize based on the magnitude of the
threat(s), then by the immediacy of the threat(s), and finally by
taxonomic status.
Under this priority-ranking system, magnitude of threat can be
either ``high'' or ``moderate to low.'' This criterion helps ensure
that the species facing the greatest threats to their continued
existence receive the highest listing priority. It is important to
recognize that all candidate species face threats to their continued
existence, so the magnitude of threats is in relative terms. For all
candidate species, the threats are of sufficiently high magnitude to
put them in danger of extinction, or make them likely to become in
danger of extinction in the foreseeable future. But for species with
higher magnitude threats, the threats have a greater likelihood of
bringing about extinction or are expected to bring about extinction on
a shorter time scale (once the threats are imminent) than for species
with lower magnitude threats. Since we do not routinely quantify how
likely or how soon extinction would be expected to occur absent
listing, we must evaluate factors that contribute to the likelihood and
time scale for extinction. We therefore consider information such as:
The number of populations and/or extent of range of the species
affected by the threat(s); the biological significance of the affected
population(s), taking into consideration the life-history
characteristics of the species and its current abundance and
distribution; whether the threats affect the species in only a portion
of its range, and if so the likelihood of persistence of the species in
the unaffected portions; the severity of the effects and the rapidity
with which they have caused or are likely to cause mortality to
individuals and accompanying declines in population levels; whether the
effects are likely to be permanent; and the extent to which any ongoing
conservation efforts reduce the severity of the threat.
As used in our priority-ranking system, immediacy of threat is
categorized as either ``imminent'' or ``nonimminent'' and is not a
measure of how quickly the species is likely to become extinct if the
threats are not addressed; rather, immediacy is based on when the
threats will begin. If a threat is currently occurring or likely to
occur in the very near future, we classify the threat as imminent.
Determining the immediacy of threats helps ensure that species facing
actual, identifiable threats are given priority for listing proposals
over those for which threats are only potential or species that are
intrinsically vulnerable to certain types of threats but are not known
to be presently facing such threats.
Our priority ranking system has three categories for taxonomic
status: Species that are the sole members of a genus; full species (in
genera that have more than one species); and subspecies and distinct
population segments of vertebrate species (DPS). We also apply this
last category to species that are threatened or endangered in only
significant portions of their ranges rather than their entire ranges.
The result of the ranking system is that we assign each candidate a
listing priority number of 1 to 12. For example, if the threat(s) is of
high magnitude, with immediacy classified as imminent, the listable
entity is assigned an LPN of 1, 2, or 3 based on its taxonomic status
(i.e., a species that is the only member of its genus would be assigned
to the LPN 1 category, a full species to LPN 2, and a subspecies, DPS,
or a species that is threatened or endangered in only a significant
portion of its range would be assigned to LPN 3). In summary, the LPN
ranking system provides a basis for making decisions about the relative
priority for preparing a proposed rule to list a given species. No
matter which LPN we assign to a species, each species included in this
notice as a candidate is one for which we have sufficient information
to prepare a proposed rule to list it because it is in danger of
extinction or likely to become endangered within the foreseeable future
throughout all or a significant portion of its range.
For more information on the process and standards used in assigning
LPNs, a copy of the 1983 guidance is available on our Web site at:
https://www.fws.gov/endangered/esa-library/pdf/48fr43098-43105.pdf. For
more information on the LPN assigned to a particular species, the
species assessment for each candidate contains the LPN chart and a
rationale for the determination of the magnitude and immediacy of
threat(s) and assignment of the LPN; that information is summarized in
this CNOR.
This revised notice supersedes all previous animal, plant, and
combined candidate notices of review.
Summary of This CNOR
Since publication of the previous CNOR on November 9, 2009 (74 FR
57804), we reviewed the available information on candidate species to
ensure that a proposed listing is justified for each species, and
reevaluated the relative LPN assigned to each species. We also
evaluated the need to emergency-list any of these species, particularly
species with high priorities (i.e., species with LPNs of 1, 2, or 3).
This review and reevaluation ensures that we focus conservation efforts
on those species at greatest risk first.
In addition to reviewing candidate species since publication of the
last CNOR, we have worked on numerous findings in response to petitions
to list species, and on proposed and final determinations for rules to
list species under the Act. Some of these findings and determinations
have been completed and published in the Federal Register, while work
on others is still under way (see Preclusion and Expeditious Progress,
below, for details).
Based on our review of the best available scientific and commercial
information, with this CNOR we identify five new candidate species (see
New Candidates, below), change the LPN for four candidates (see Listing
Priority Changes in Candidates, below) and determine that a listing
proposal is not warranted for one species and thus remove it from
candidate status (see
[[Page 69224]]
Candidate Removals, below). Combined with the other decisions published
separately from this CNOR for individual species that previously were
candidates, a total of 251 species (including 110 plant and 141 animal
species) are now candidates awaiting preparation of rules proposing
their listing. These 251 species, along with the 18 species currently
proposed for listing (includes 1 species proposed for listing due to
similarity in appearance), are included in Table 1.
Table 2 lists the changes from the previous CNOR, and includes 55
species identified in the previous CNOR as either proposed for listing
or classified as candidates that are no longer in those categories.
This includes 54 species for which we published a final rule to list,
plus the 1 species that we have determined does not meet the definition
of endangered or threatened and therefore does not warrant listing. We
have removed this species from candidate status in this CNOR.
New Candidates
Below we present a brief summary of one new fish, one new snail,
one new crustacean, and two new plant candidates, which we are
recognizing in this CNOR. Complete information, including references,
can be found in the species assessment forms. You may obtain a copy of
these forms from the Regional Office having the lead for the species,
or from our Web site (https://ecos.fws.gov/tess_public/pub/SpeciesReport.do?listingType=C&mapstatus=1). For these species, we find
that we have on file sufficient information on biological vulnerability
and threats to support a proposal to list as endangered or threatened,
but that preparation and publication of a proposal is precluded by
higher priority listing actions (i.e., it met our definition of a
candidate species). We also note below that nine other species--
Sprague's pipit, greater sage-grouse, Bi-State DPS of greater sage-
grouse, Gunnison sage-grouse, least chub, upper Missouri River DPS of
Arctic grayling, Tucson shovel-nosed snake, Jemez Mountains salamander,
and Agave eggersiana--were identified as candidates earlier this year
as a result of separate petition findings published in the Federal
Register.
Birds
Sprague's pipit (Anthus spragueii)--We previously announced
candidate status for this species, and described the reasons and data
on which the finding was based, in a separate warranted-but-precluded
12-month petition finding published on September 14, 2010 (75 FR
56028).
Greater sage-grouse (Centrocercus urophasianus)--We previously
announced candidate status for this species, and described the reasons
and data on which the finding was based, in a separate warranted-but-
precluded 12-month petition finding published on March 23, 2010 (75 FR
13910).
Greater sage-grouse, Bi-State DPS (Centrocercus urophasianus)--We
previously announced candidate status for this species, and described
the reasons and data on which the finding was based, in a separate
warranted-but-precluded 12-month petition finding published on March
23, 2010 (75 FR 13910).
Gunnison sage-grouse (Centrocercus minimus)--We previously
announced candidate status for this species, and described the reasons
and data on which the finding was based, in a separate warranted-but-
precluded 12-month petition finding published on September 28, 2010 (75
FR 59803).
Reptiles
Tucson Shovel-Nosed Snake (Chionactis occipitalis klauberi)--We
previously announced candidate status for this species, and described
the reasons and data on which the finding was based, in a separate
warranted-but-precluded 12-month petition finding published on March
31, 2010 (75 FR 16050).
Amphibians
Jemez Mountains salamander (Plethodon neomexicanus)--We previously
announced candidate status for this species, and described the reasons
and data on which the finding was based, in a separate warranted-but-
precluded 12-month petition finding published on September 9, 2010 (75
FR 54822).
Fish
Least chub (Iotichthys phlegethontis)--We previously announced
candidate status for this species, and described the reasons and data
on which the finding was based, in a separate warranted-but-precluded
12-month petition finding published on June 22, 2010 (75 FR 35398).
Kentucky arrow darter (Etheostoma sagitta spilotum)--The following
summary is based on information in our files. The Kentucky arrow darter
is a rather large (total length of 4.6 inches (116 millimeters)),
brightly colored darter that is restricted to the upper Kentucky River
basin in eastern Kentucky. The species' preferred habitat consists of
pools or transitional areas between riffles and pools (runs and glides)
in moderate to high gradient streams with bedrock, boulder, and cobble
substrates. In most recent surveys, the Kentucky arrow darter has been
observed in streams ranging in size from first to third order, with
most individuals occurring in second order streams in watersheds
encompassing 7.7 square miles (20 square kilometers) or less. Kentucky
arrow darters feed on a variety of aquatic invertebrates, but adults
feed predominantly on larval mayflies (order Ephemeroptera),
specifically the families Heptageniidae and Baetidae. Rangewide surveys
from 2007 to 2009 revealed that the Kentucky arrow darter has
disappeared from portions of its range. During these surveys, the
species was observed at only 33 of 68 historical streams and 45 of 100
historical sites.
The subspecies' habitat and range have been severely degraded and
limited by water pollution from surface coal mining and gas-exploration
activities; removal of riparian vegetation; stream channelization;
increased siltation associated with poor mining, logging, and
agricultural practices; and deforestation of watersheds. The threats
are high in magnitude because they are widespread across the
subspecies' range. In addition, the magnitude (severity or intensity)
of these threats, especially impacts from mining and gas-exploration
activities, is high because these activities have the potential to
alter stream water quality permanently throughout the range by
contributing sediment, dissolved metals, and other solids to streams
supporting Kentucky arrow darters, resulting in direct mortality or
reduced reproductive capacity. The threats are imminent because the
effects are manifested immediately and will continue for the
foreseeable future. Consequently, we assigned an LPN of 3 to this
subspecies.
Arctic grayling, Missouri River DPS (Thymallus arcticus)--We
previously announced candidate status for this species, and described
the reasons and data on which the finding was based, in a separate
warranted-but-precluded 12-month petition finding published on
September 8, 2010 (75 FR 54707).
Snails
Rosemont talussnail (Sonorella rosemontensis)--the following
summary is based on information in our files. The petition we received
on June 24, 2010, provided no new information beyond what we had
already included in our assessment of this species. The Rosemont
talussnail, a land snail in the family Helminthoglyptidae, is known
[[Page 69225]]
from three talus slopes in the Santa Rita Mountains, Pima County,
Arizona. The primary threat to Rosemont talussnail is hard rock mining.
The entire range of the species is located on patented mining claims
and can reasonably be expected to be subjected to mining activities in
the foreseeable future. Hard rock mining typically involves the
blasting of hillsides and the crushing of ore-laden rock. Such
activities would kill talussnails and render their habitats unsuitable
for occupation. Since mining may occur across the entire range of the
species within the foreseeable future, potentially resulting in
rangewide habitat destruction and population losses, the threats are of
a high magnitude. However, mining on patented mining claims, although a
reasonably anticipated action, is neither currently ongoing nor
imminent. Although the Rosemont Copper Mine is scheduled to commence as
soon as 2011, there exists uncertainty regarding its scope, and
therefore its potential effect on habitat of the Rosemont talussnail.
Accordingly, we find that overall threats to the Rosemont talussnail
are nonimminent and we assign an LPN of 5 to this species.
Crustaceans
Kenk's amphipod (Stygobromus kenki)--Amphipods of the genus
Stygobromus, occur in groundwater and groundwater-related habitats. In
the case of Kenk's amphipod, these include seeps, small springs, and
possibly wells. Kenk's amphipod is a small, eyeless, unpigmented
crustacean adapted for survival in subterranean habitats. It can be
found in dead leaves or fine sediment submerged in the waters of its
spring/seep outflows. The species is currently known only from five
spring or seep sites in Washington, DC, and Montgomery County,
Maryland. Four of these sites are within the Rock Creek drainage, and
the fifth is within the Northwest Branch drainage.
Within the limited area encompassing the current range of this
species, the vast majority of potential expanses of habitat large
enough to support this species have been significantly impacted or
completely destroyed by urban and suburban development. Kenk's amphipod
is now vulnerable because of its limited geographic distribution and
infringement of urban development on its habitat. Degradation of water
quality and modifications of hydrology are among the principal threats
to this species' spring or seep habitats. Specific threats include
toxic spills, non-point source pollution, sanitary sewer leaks,
excessive stormwater flows, and additional land disturbance. In
addition, climate change has the potential to adversely affect the
species, particularly if it results in a significant change in the
amount of precipitation in the Washington, DC, area.
Although all five known sites of occurrence face threats to the
hydrology and water quality of their springs, these threats are chronic
in nature and appear to be increasing only gradually and are not
currently resulting in major mortality events or impairment of
reproduction. Thus, the threats are moderate in magnitude. Several
threats are imminent because they are ongoing and expected to continue.
Therefore, we assigned this species LPN of 8.
Flowering Plants
Agave eggersiana (no common name)--We previously announced
candidate status for this species, and described the reasons and data
on which the finding was based, in a separate warranted-but-precluded
12-month petition finding published on September 22, 2010 (75 FR
57720).
Astragalus cusickii var. packardiae (Packard's milkvetch)--The
following summary is based on information contained in our files. This
plant is a narrow endemic located in northeastern Payette County,
Idaho. Its entire known range is only approximately 10 square miles (26
square kilometers). The light-colored, sparsely vegetated sedimentary
outcrops to which this species is restricted are found scattered
throughout the landscape, but are limited in extent. The size of
occupied outcrops ranges from less than 0.04 hectares (0.1 acre) to
approximately 1.2 hectares (3 acres). The entire population of A.
cusickii var. packardiae is currently estimated at 5,000 plants located
within 26 occurrences (17 on Bureau of Land Management, 4 on State, and
5 on private land).
The primary threats to Astragalus cusickii var. packardiae include
wildfire, nonnative invasive plant species, and more recently, off-road
vehicle (ORV) use. Vegetation within the range of A. cusickii var.
packardiae was originally sagebrush-steppe habitat; however, due to
habitat impacts from a century of wildfires, livestock use, and
invasive nonnative plant species, much of the area has been converted
to annual grassland dominated by two nonnative grass species, Bromus
tectorum (cheatgrass) and Taeniatherum caput-medusae (medusahead).
Invasive nonnative plants affect A. cusickii var. packardiae directly
through competition and indirectly by providing continuous fine fuels
that contribute to the increased frequency and extent of wildfires.
ORV use, which is currently considered the most immediate threat to
Astragalus cusickii var. packardiae and its habitat, was not identified
as a threat during the original 1999 surveys for this species, but
monitoring conducted in 2008 and 2009 indicate it has since become a
widespread activity, occurring throughout the limited range of A.
cusickii var. packardiae. ORVs are traveling directly through outcrops
occupied by A. cusickii var. packardiae, as well as along the rims,
spur ridges, and slope bases that form the margins of the occupied
outcrops, with tracks ranging from single passage treads to major hill
climbing runways. Based on monitoring data, this use appears to be
increasing in scope and has resulted in the crushing of A. cusickii
var. packardiae plants, as well as accelerated erosion of the fine,
loose substrate occupied by this species.
Based on this information, the magnitude of the primary threats to
Astragalus cusickii var. packardiae and its habitat is high because ORV
use, wildfires, and nonnative invasive species affect the species
throughout its range, appear to be increasing in extent, and result in
severe and direct impacts to individuals and population levels.,
Because these threats are ongoing throughout A. cusickii var.
packardiae's limited range, these threats are imminent. Thus, we assign
an LPN of 3 to this plant variety.
Mimulus fremontii var. vandenbergensis (Vandenberg monkeyflower)--
Mimulus fremontii var. vandenbergensis is a small, short-lived annual
herb in the Phrymaceae family (no common family name). It ranges from
0.5 to 10 inches (1 to 20 centimeters) tall and produces flowers that
are bright yellow with reddish brown markings near the mouth. The seeds
are small and numerous, and seed is likely dispersed by the wind as the
seed pods open. As with other annual species that are sensitive to
annual levels of rainfall, germination of resident seed banks may be
low or nonexistent in unfavorable years, with little or no aboveground
expression of the species visible.
Mimulus fremontii var. vandenbergensis occurs only in western Santa
Barbara County, California, at lower elevations and closer to the
coast, in sandy openings of coastal scrub, chaparral, and woodlands on
an old dune sheet known as Burton Mesa. Seven populations occur across
the mesa over a distance of approximately 6 miles, generally in
alignment with the prevailing winds. Two populations
[[Page 69226]]
occur on Vandenberg Air Force Base, two occur on State Park lands at La
Purisima State Historic Park, two occur primarily on Department of Fish
and Game lands on Burton Mesa Ecological Reserve, and one occurs
primarily on private lands.
The threats currently facing Mimulus fremontii var. vandenbergensis
include alteration and destruction of habitat from development and
associated secondary impacts, including increased fragmentation,
alteration of hydrology, competition with nonnative species, and
alteration of fire regimes. The taxon is also threatened with
stochastic extinction due to small population size: Of the 7
populations, 3 have supported fewer than 100 individuals based on at
least 2 years of observations. We consider competition with nonnative
plant species to be the largest and most immediate threat: Veldt grass,
pampas grass, bromes, Sahara mustard, star thistle, Italian thistle,
and bull thistle are present at various sites where Mimulus fremontii
var. vandenbergensis occurs. Habitat for one population on private land
was graded in 2007 in preparation for construction of a housing
development. Construction has been stalled, and in the meantime, veldt
grass has become established in the graded lot and has increased the
rate at which this species is spreading in adjacent habitat for Mimulus
fremontii var. vandenbergensis, including the Burton Mesa Ecological
Reserve. Veldt grass is also present and rapidly spreading at
population sites on Vandenberg Air Force Base and La Purisima State
Historic Park.
The threats are of a high magnitude because all three of the
largest populations are at risk of being lost from the invasion of
nonnative species. The third largest population is also threatened by
secondary impacts from a planned development and firefighting
activities. Losses of some or all of the three largest populations will
increase the risk of extinction of the taxon as a whole because the
remaining populations are smaller and more vulnerable to stochastic
extirpation, which compounds the other threats these small populations
face. The threats are ongoing and, therefore, imminent. Consequently,
we have assigned a LPN of 3 to this plant variety.
Listing Priority Changes in Candidates
We reviewed the LPN for all candidate species and are changing the
numbers for the following species discussed below. Some of the changes
reflect actual changes in either the magnitude or immediacy of the
threats. For some species, the LPN change reflects efforts to ensure
national consistency as well as closer adherence to the 1983 guidelines
in assigning these numbers, rather than an actual change in the nature
of the threats.
Snails
Page springsnail (Pyrgulopsis morrisoni)--The following summary is
based on information contained in our files. The Page springsnail is
known to exist only within a complex of springs located within an
approximately 0.93-mi (1.5-km) stretch along the west side of Oak Creek
around the community of Page Springs, and within springs located along
Spring Creek, tributary to Oak Creek, Yavapai County, Arizona.
The primary threat to the Page springsnail is modification of
habitat by domestic, agricultural, ranching, fish hatchery, and
recreational activities. Many of the springs where the species occurs
have been subjected to some level of such modification. Based on recent
survey data, it appears that the Page springsnail is abundant within
natural habitats and persists in modified habitats, albeit at reduced
densities. Arizona Game and Fish Department (AGFD) management plans for
the Bubbling Ponds and Page Springs fish hatcheries include commitments
to replace lost habitat and to monitor remaining populations of
invertebrates such as the Page springsnail. The AGFD and the Service
recently entered into a Candidate Conservation Agreement with
Assurances that calls for evaluating the restoration and creation of
natural springhead integrity, including springs on AGFD properties. In
fact, several conservation measures have already been implemented.
Also, the National Park Service recently acquired Shea Springs, a site
that the Page springsnail occupied historically, and has expressed an
interest in restoring natural springhead integrity to that site.
Accordingly, implementation of the CCAA reduces the magnitude of
threats to a moderate level and greatly reduces the chances of
extirpation or extinction. The immediacy of the threat of groundwater
withdrawal is uncertain, due to conflicting information regarding
imminence. However, overall, the threats are imminent, because
modification of the species' habitat by threats other than groundwater
withdrawal is currently occurring. Therefore, we are changing the LPN
for the Page springsnail from a 2 to an 8.
Flowering Plants
Hibiscus dasycalyx (Neches River rose-mallow)--The following
summary is based on information contained in our files. This species,
found in eastern Texas, appears to be restricted to those portions of
wetlands that are exposed to open sun and normally hold standing water
early in the growing season, with water levels dropping during late
summer and fall. This habitat has been affected by drainage or filling
of floodplain depressions and oxbows, stream channelization, road
construction, timber harvesting, agricultural activities (primarily
mowing and grazing), and herbicide use. Threats that continue to affect
the species include wetland alteration, herbicide use, grazing, mowing
during the species' growing and flowering period, and genetic swamping
by other Hibiscus species.
A 1995 status survey of 10 counties resulted in confirmation of the
species at only three sites, but in three separate counties and three
different watersheds, suggesting a relatively wide historical range.
These three populations were all within highway rights-of-way and
vulnerable to herbicides and adjacent agricultural activities. As of
2005, only 20 plants remained at one of these sites. Additional surveys
for Hibiscus dasycalyx discovered new populations. About 300 plants
were found on land owned by Temple-Inland Corporation in east Trinity
County. Smaller plant numbers have been seen at this site and in 2005
no plants were observed. This site may be too dry to support this
species, possibly due to changes in the wetland's hydrology. Another
site discovered on land previously owned by Champion International
Corporation (near White Rock Creek in west Trinity County) once
supported 300-400 plants. This site was modified in 2007. In west
Houston County, a population of 300 to 400 plants discovered on private
land has been purchased by the Natural Area Preservation Association in
order to protect this land in perpetuity. In east Houston County, a
population discovered in Compartment 55 in Davy Crockett National
Forest numbered over 1,000 in 2006. In 2000, nearly 800 plants were
introduced into Compartments 16 and 20 of Davy Crockett National Forest
as part of a reintroduction effort. One population retained high
numbers (350 in 2006), but was subjected to high water conditions in
2007 and may have been adversely affected. The second site was affected
by a change in hydrology and had declined to 50 plants in 2006. In
2004, 200 plants were placed in a wetland in Compartment 11 of Davy
Crockett National Forest, but only 10 plants were seen in 2006. High
water from heavy spring and summer rains
[[Page 69227]]
prevented further assessment of these rose-mallow sites.
The threats to the species continue to be of a high magnitude
because all of the populations are severely affected by some
combination of the threats, and the effectiveness of the re-
introduction and preservation efforts has not been established. After
evaluating the current conditions of the species' habitat, we now find
that threats are imminent overall. Threats are currently occurring and
ongoing for nearly all of the populations (herbicides and adjacent
agricultural activities for the 3 populations identified in 1995, and
hydrology alteration and other modifications for the 2 populations in
east Trinity County and the 3 populations reintroduced in Davy Crockett
National Forest). Thus, in light of this information and to ensure
consistency in the application of our listing priority process we have
changed the LPN from a 5 to a 2 for the Neches River rose-mallow to
reflect imminent threats of high magnitude.
Linum arenicola (Sand flax)--The following summary is based on
information contained in our files. Sand flax is found in pine rockland
and marl prairie habitats, which require periodic wildfires in order to
maintain an open, shrub-free subcanopy and reduce leaf-litter levels.
Based upon available data, there are 11 extant occurrences of sand
flax; 11 others have been extirpated or destroyed. For the most part,
only small and isolated occurrences remain in low lying areas in a
restricted range of southern Florida and the Florida Keys. In general,
viability is uncertain for 9 of 11 occurrences.
Sand flax is threatened by habitat loss and degradation due to
development; climatic changes and sea-level rise, which ultimately are
likely to substantially reduce the extent of available habitat; fire
suppression and difficulty in applying prescribed fire; road
maintenance activities; exotic species; illegal dumping; natural
disturbances, such as hurricanes, tropical storms, and storm surges;
and the small and fragmented nature of the current population. Reduced
pollinator activity and suppression of pollinator populations from
pesticides used in mosquito control and decreased seed production due
to increased seed predation in a fragmented wildland urban interface
may also affect sand flax; however, not enough information is known on
this species' reproductive biology or life history to assess these
potential threats. Some of the threats to the species--including fire
suppression, difficulty in applying prescribed fire, road maintenance
activities, exotic species, and illegal dumping--threaten nearly all
remaining populations. However, some efforts are under way to use
prescribed fire to control exotics on conservation lands where this
species occurs.
There are some circumstances that may mitigate the impacts of the
threats upon the species. For example, a survey conducted in 2009
showed approximately 74,000 plants on a non-conservation, public site
in Miami-Dade County; this is far more plants than was previously
known. Although a portion of the plants will be affected by
development, approximately 60,000 are anticipated to be protected and
managed through a Conservation Easement. Consequently, the majority of
the largest occurrence in Miami-Dade County is expected to be conserved
and managed. In addition, much of the pine rockland on Big Pine Key,
the location of the largest occurrence in the Keys, is protected from
development.
Nevertheless, due to the small and fragmented nature of the current
population, stochastic events, disease, or genetic bottlenecks may
strongly affect this species in the Keys. One example is Hurricane
Wilma, which inundated most of the species' habitat on Big Pine Key in
2005, and plants were not found 8-9 weeks post-storm; the density of
sand flax declined to zero in all management units at The Nature
Conservancy's preserve in 2006. In a 2007 post-hurricane assessment,
sand flax was found in northern plots, but not in any of the southern
plots on Big Pine Key. More current data are not available.
Overall, the magnitude of threats is high, because the threats
affect all 11 known occurrences of the species, and can result in a
precipitous decline to the population levels, particularly when
combined with the potential impacts from hurricanes or other natural
disasters. Because development is not immediate for the majority of the
largest population in Miami-Dade County and another population in the
Keys is also largely protected from development since much of it is
within public and private conservation lands, the threat of habitat
loss is now nonimminent. In addition, sea level rise is a long-term
threat since we do not have evidence that it is currently affecting any
population of sand flax. Therefore, based upon new information (new
survey date showing a much larger population of plants), and reduced
immediacy of threats, we changed the LPN of this species from a 2 to a
5.
Penstemon scariosus var. albifluvis (White River beardtongue)--The
following summary is based on information contained in our files and
the petition we received on October 27, 1983. This species is
restricted to calcareous soils derived from oil shale barrens of the
Green River Formation in the Uinta Basin of northeastern Utah and
adjacent Colorado. There are 14 occurrences known in Utah and 1 in
Colorado. Most of the occupied habitat of the White River beardtongue
is within developed and expanding oil and gas fields. The location of
the species' habitat exposes it to destruction from road, pipeline, and
well site construction in connection with oil and gas development.
Recreational off-road vehicle use, heavy grazing by livestock, and
wildlife and livestock trampling are additional threats. A future
threat (and potentially the greatest threat) to the species is oil
shale development.
In the 2009 CNOR, we found the threats were nonimminent and high
magnitude. However, traditional oil and gas energy development in the
area has expanded into habitat for this species, and therefore the
threat is now imminent. In addition, BLM has adopted a Special Status
Species policy and has included in its current Resource Management Plan
commitments to protect this species. These protections lessen the
extent of traditional oil and gas development impacts to this species,
so that the threat is now of moderate magnitude. The threat from off-
road vehicles is also moderate because BLM limited all vehicles to
designated routes, thus avoiding beardtongue habitat. Based on current
information, we are changing the LPN from a 6 to a 9 for this plant
variety.
Candidate Removals
As summarized below, we have evaluated the threats to the following
species and considered factors that, individually and in combination,
currently or potentially could pose a risk to this species and its
habitat. After a review of the best available scientific and commercial
data, we conclude that listing this species under the Endangered
Species Act is not warranted because the species is not likely to
become an endangered species within the foreseeable future throughout
all or a significant portion of its' range. Therefore, we find that
proposing a rule to list it is not warranted, and we no longer consider
it to be a candidate species for listing. We will continue to monitor
the status of this species and to accept additional information and
comments concerning this finding. We will reconsider our determination
in the event that new information indicates that the threats to the
species is of a considerably greater magnitude or imminence than
identified through
[[Page 69228]]
assessments of information contained in our files, as summarized here.
Mammals
Palm Springs round-tailed ground squirrel (Xerospermophilus
tereticaudus chlorus)--The following summary is based on information
contained in our files. No new information was provided in the petition
we received on May 11, 2004. The Palm Springs round-tailed ground
squirrel was believed to be limited in range to the Coachella Valley
region of Riverside County, California. The primary habitat in the
Coachella Valley for round-tailed ground squirrel is the dunes and
mesquite hummocks associated with Prosopis glandulosa var. torreyana
(honey mesquite) and to a lesser extent those dunes and hummocks
associated with Larrea tridentata (creosote), or other vegetation. The
primary threat to X. t. chlorus in the Coachella Valley was from
habitat loss due to urban development and drops in the groundwater
table, which eliminated much of the honey mesquite in the Coachella
Valley and fragmented habitat occupied by this subspecies. The
Coachella Valley Association of Governments (CVAG) developed a Multiple
Species Habitat Conservation Plan (MSHCP) that was reviewed and
approved by the Service in 2008. Habitat conservation and monitoring
actions that have been implemented since 2008 specifically for X. t.
chlorus have significantly eliminated the threat of urban development
to the taxon. To date, conservation for X. t. chlorus includes
protection of 244 acres of mesquite hummocks as a result of the MSHCP,
in addition to 104 acres of mesquite hummocks on conservation lands in
existence prior to permitting the MSHCP. Protection of additional
habitat (desert shrub communities and other sandy areas with
appropriate vegetation known to harbor the subspecies at lower
densities) is also anticipated in other portions of the plan area.
Although we do not rely upon future implementation of the additional
habitat protections anticipated in the MSHCP, we do expect conservation
actions specific to X. t. chlorus to continue as a result of the
commitment by CVAG and the MSHCP.
More significant than the ongoing conservation measures is the fact
that recent results of both morphological and genetic studies indicate
its range is substantially larger than previously believed. Analysis of
experimental samples show X. t. chlorus is found in Hinkley Valley and
Death Valley, expanding the range at minimum 150 miles northward.
Because X. t. chlorus is more widespread in its range than was
previously understood, and based on our review of the best available
information, we no longer conclude that threats across this newly
expanded range put the taxon in danger of extinction. Moreover, this
subspecies is not endangered or threatened in a significant portion of
the range because the conservation actions and current protections
provided in Death Valley make it so it is not endangered or threatened
in any portion of the range. In summary, the existing conservation
provided by MSHCP in the Coachella Valley, along with the data showing
the subspecies has an expanded range over which the threats are
nonsignificant to the taxon as a whole, we find listing of the Palm
Springs round-tailed ground squirrel (X. t. chlorus) throughout all or
a significant portion of its range is no longer warranted. The
subspecies no longer meets our definition of a candidate, and we have
removed it from candidate status.
Petition Findings
The Act provides two mechanisms for considering species for
listing. One method allows the Secretary, on his own initiative, to
identify species for listing under the standards of section 4(a)(1). We
implement this through the candidate program, discussed above. The
second method for listing a species provides a mechanism for the public
to petition us to add a species to the Lists. The CNOR serves several
purposes as part of the petition process: (1) In some instances (in
particular, for petitions to list species that the Service has already
identified as candidates on its own initiative), it serves as the
petition finding; (2) it serves as a ``resubmitted'' petition finding
that the Act requires the Service to make each year; and (3) it
documents the Service's compliance with the statutory requirement to
monitor the status of species for which listing is warranted-but-
precluded to ascertain if they need emergency listing.
First, the CNOR serves as a petition finding in some instances.
Under section 4(b)(3)(A), when we receive a listing petition, we must
determine within 90 days, to the maximum extent practicable, whether
the petition presents substantial information indicating that listing
may be warranted (a ``90-day finding''). If we make a positive 90-day
finding, we must promptly commence a status review of the species under
section 4(b)(3)(A); we must then make and publish one of three possible
findings within 12 months of the receipt of the petition (a ``12-month
finding''):
1. The petitioned action is not warranted;
2. The petitioned action is warranted (in which case we are
required to promptly publish a proposed regulation to implement the
petitioned action; once we publish a proposed rule for a species,
section 4(b)(5) and 4(b)(6) govern further procedures regardless of
whether we issued the proposal in response to a petition); or
3. The petitioned action is warranted but (a) the immediate
proposal of a regulation and final promulgation of a regulation
implementing the petitioned action is precluded by pending proposals to
determine whether any species is endangered or threatened, and (b)
expeditious progress is being made to add qualified species to the
lists of endangered or threatened species. (We refer to this third
option as a ``warranted-but-precluded finding.'')
We define ``candidate species'' to mean those species for which the
Service has on file sufficient information on biological vulnerability
and threat(s) to support issuance of a proposed rule to list, but for
which issuance of the proposed rule is precluded (61 FR 64481; December
6, 1996). This standard for making a species a candidate through our
own initiative is identical to the standard for making a warranted-but-
precluded 12-month petition finding on a petition to list, and we add
all petitioned species for which we have made a warranted-but-precluded
12-month finding to the candidate list.
Therefore all candidate species identified through our own
initiative already have received the equivalent of substantial 90-day
and warranted-but-precluded 12-month findings. Nevertheless, we review
the status of the newly petitioned candidate species and through this
CNOR publish specific section 4(b)(3) findings (i.e., substantial 90-
day and warranted-but-precluded 12-month findings) in response to the
petitions to list these candidate species. We publish these findings as
part of the first CNOR following receipt of the petition. Since
publication of the CNOR in 2009, we received petitions to list three
candidate species, the Florida bonneted bat, headwater chub, and
Rosemont talussnail (we received this petition after we initiated our
assessment of this species for candidate status). We are making
substantial 90-day findings and warranted-but-precluded 12-month
findings for these species as part of this notice. We have identified
the candidate species for which we received petitions by the code
``C*'' in the category column on the left side of Table 1.
[[Page 69229]]
Second, the CNOR serves as a ``resubmitted'' petition finding.
Section 4(b)(3)(C)(i) of the Act requires that when we make a
warranted-but-precluded finding on a petition, we are to treat such a
petition as one that is resubmitted on the date of such a finding.
Thus, we must make a 12-month petition finding in compliance with
section 4(b)(3)(B) of the Act at least once a year, until we publish a
proposal to list the species or make a final not-warranted finding. We
make these annual findings for petitioned candidate species through the
CNOR.
Third, through undertaking the analysis requires to complete the
CNOR, the Service determines if any candidate species needs emergency
listing. Section 4(b)(3)(C)(iii) of the Act requires us to ``implement
a system to monitor effectively the status of all species'' for which
we have made a warranted-but-precluded 12-month finding, and to ``make
prompt use of the [emergency listing] authority [under section 4(b)(7)]
to prevent a significant risk to the well being of any such species.''
The CNOR plays a crucial role in the monitoring system that we have
implemented for all candidate species by providing notice that we are
actively seeking information regarding the status of those species. We
review all new information on candidate species as it becomes
available, prepare an annual species assessment form that reflects
monitoring results and other new information, and identify any species
for which emergency listing may be appropriate. If we determine that
emergency listing is appropriate for any candidate we will make prompt
use of the emergency listing authority under section 4(b)(7). We have
been reviewing and will continue to review, at least annually, the
status of every candidate, whether or not we have received a petition
to list it. Thus, the CNOR and accompanying species assessment forms
constitute the Service's annual finding on the status of petitioned
species pursuant to section 4(b)(3)(C)(i).
A number of court decisions have elaborated on the nature and
specificity of information that must be considered in making and
describing the findings in the CNOR. The previous CNOR, which was
published on November 9, 2009 (74 FR 57804), describes these court
decisions in further detail. As with previous CNORs, we continue to
incorporate information of the nature and specificity required by the
courts. For example, we include a description of the reasons why the
listing of every petitioned candidate species is both warranted and
precluded at this time. We 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 (see below). Regional priorities can also be
discerned from Table 1, which includes the lead region and the LPN for
each species. Our preclusion determinations are further based upon our
budget for listing activities for unlisted species only, and we explain
the priority system and why the work we have accomplished does preclude
action on listing candidate species.
Pursuant to section 4(b)(3)(C)(ii) and the Administrative Procedure
Act (5 U.S.C. 551 et seq.), any party with standing may challenge the
merits of any not-warranted or warranted-but-precluded petition finding
incorporated in this CNOR. The analysis included herein, together with
the administrative record for the decision at issue (particularly the
supporting species assessment form), will provide an adequate basis for
a court to review the petition finding.
Nothing in this document or any of our policies should be construed
as in any way modifying the Act's requirement that we make a
resubmitted 12-month petition finding for each petitioned candidate
within 1 year of the date of publication of this CNOR. If we fail to
make any such finding on a timely basis, whether through publication of
a new CNOR or some other form of notice, any party with standing may
seek judicial review.
In this CNOR, we continue to address the concerns of the courts by
including specific information in our discussion on preclusion (see
below). In preparing this CNOR, we reviewed the current status of, and
threats to, the 166 candidates and 5 listed species for which we have
received a petition and for which we have found listing or
reclassification from threatened to endangered to be warranted but
precluded. We also reviewed the current status of, and threats to, the
Canada lynx in New Mexico for which we received a petition to add that
State to the listed range. We find that the immediate issuance of a
proposed rule and timely promulgation of a final rule for each of these
species has been, for the preceding months, and continues to be,
precluded by higher priority listing actions. Additional information
that is the basis for this finding is found in the species assessments
and our administrative record for each species.
Our review included updating the status of, and threats to,
petitioned candidate or listed species for which we published findings,
pursuant to section 4(b)(3)(B), in the previous CNOR. We have
incorporated new information we gathered since the prior finding and,
as a result of this review, we are making continued warranted-but-
precluded 12-month findings on the petitions for these species.
The immediate publication of proposed rules to list these species
was precluded by our work on higher priority listing actions, listed
below, during the period from October 1, 2009, through September 30,
2010. We will continue to monitor the status of all candidate species,
including petitioned species, as new information becomes available to
determine if a change in status is warranted, including the need to
emergency-list a species under section 4(b)(7) of the Act.
In addition to identifying petitioned candidate species in Table 1
below, we also present brief summaries of why each of these candidates
warrants listing. More complete information, including references, is
found in the species assessment forms. You may obtain a copy of these
forms from the Regional Office having the lead for the species, or from
the Fish and Wildlife Service's Internet Web site: https://ecos.fws.gov/tess_public/pub/SpeciesReport.do?listingType=C&mapstatus=1. As
described above, under section 4 of the Act we may identify and propose
species for listing based on the factors identified in section 4(a)(1),
and section 4 also provides a mechanism for the public to petition us
to add a species to the lists of threatened species or endangered
species under the Act. Below we describe the actions that continue to
preclude the immediate proposal and final promulgation of a regulation
implementing each of the petitioned actions for which we have made a
warranted-but-precluded finding, and we describe the expeditious
progress we are making to add qualified species to, and remove species
from, the lists of endangered or threatened species.
Preclusion and Expeditious Progress
Preclusion is a function of the listing priority of a species in
relation to the resources that are available and the cost and relative
priority of 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 listing proposal regulation or whether
promulgation of such a proposal is precluded by higher priority listing
actions.
The resources available for listing actions are determined through
the annual Congressional appropriations
[[Page 69230]]
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 ``resubmitted'' petition findings on prior
warranted-but-precluded petition findings as required under section
4(b)(3)(C)(i) of the Act; critical habitat petition findings; proposed
and final rules designating critical habitat; and litigation-related,
administrative, and program-management functions (including preparing
and allocating budgets, responding to Congressional and public
inquiries, and conducting public outreach regarding listing and
critical habitat). The work involved in preparing various listing
documents can be extensive, and may include, but is not limited to:
Gathering and assessing the best scientific and commercial data
available and conducting analyses used as the basis for our decisions;
writing and publishing documents; and obtaining, reviewing, and
evaluating public comments and peer-review comments on proposed rules
and incorporating relevant information into final rules. The number of
listing actions that we can undertake in a given year also is
influenced by the complexity of those listing actions; that is, more
complex actions generally are more costly. The median cost for
preparing and publishing a 90-day finding is $39,276; for a 12-month
finding, $100,690; for a proposed rule with critical habitat, $345,000;
and for a final listing rule with critical habitat, the median cost is
$305,000.
We cannot spend more than is appropriated for the Listing Program
without violating the Anti-Deficiency Act (see 31 U.S.C.
1341(a)(1)(A)). In addition, in FY 1998 and for each fiscal year since
then, Congress has placed a statutory cap on funds which may be
expended for the Listing Program, equal to the amount expressly
appropriated for that purpose in that fiscal year. This cap was
designed to prevent funds appropriated for other functions under the
Act (for example, recovery funds for removing species from the Lists),
or for other Service programs, from being used for Listing Program
actions (see House Report 105-163, 105th Congress, 1st Session, July 1,
1997).
Since FY 2002, the Service's budget has included a critical habitat
subcap to ensure that some funds are available for other work in the
Listing Program (``The critical habitat designation subcap will ensure
that some funding is available to address other listing activities''
(H.R. 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 court-mandated
designations of critical habitat, and consequently none of the critical
habitat subcap funds have been available for other listing activities.
In FY 2007, we were able to use some of the critical habitat subcap
funds to fund proposed listing determinations for high-priority
candidate species. In FY 2009, while we were unable to use any of the
critical habitat subcap funds to fund proposed listing determinations,
we did use some of this money to fund the critical habitat portion of
some proposed listing determinations so that the proposed listing
determination and proposed critical habitat designation could be
combined into one rule, thereby being more efficient in our w