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, 57804-57878 [E9-26841]
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DEPARTMENT OF THE INTERIOR
Fish and Wildlife Service
50 CFR Part 17
[Docket No. FWS-R9-ES-2009-0075; MO9221050083–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
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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 remove species 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
eight candidates, and removes four
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 249.
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
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October 1, 2008, through September 30,
2009.
We request additional status
information that may be available for
the 249 candidate species identified in
this CNOR.
DATES: We will accept information on
this Candidate Notice of Review at any
time.
ADDRESSES: This notice is available on
the Internet at https://
www.regulations.gov, and https://
endangered.fws.gov/candidates/
index.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 Internet
website (https://endangered.fws.gov/
candidates/). 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 in preparing listing
documents and future revisions to the
notice of review, as it will help us in
monitoring changes in the status of
candidate species and in management
for conserving them. 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
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for public inspection by appointment,
during normal business hours, at the
appropriate Regional Office listed below
in 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. A species may be indentified by
us as a candidate for listing based on an
evaluation of its status that we
conducted on our own initiative, or as
a result of making a finding on a
petition to list a species 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
require protection under the Act or
additional species that may require the
Act’s protections; and to request
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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 in
SUPPLEMENTARY INFORMATION or visit our
Internet website, https://
endangered.fws.gov/candidates/
index.html.
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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 December 10,
2008 (73 FR 75176). CNORs published
since 1994 are available on our Internet
website, https://www.fws.gov/
endangered/candidates/. 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).
Guidelines for such a priority-ranking
guidance system is required under
section 4(h)(3) of the Act (15 U.S.C.
1533(h)(3)). 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. When
evaluating the magnitude of the threat(s)
facing the species, we 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;
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and whether the effects are likely to be
permanent.
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. 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 guidance is available on
our website at: https://www.fws.gov/
endangered/policy/. 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
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imminence 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 CNOR on
December 10, 2008 (73 FR 75176), 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 eight candidates (see Listing
Priority Changes in Candidates, below)
and determine that listing proposals are
not warranted for four species and thus
remove them from candidate status (see
Candidate Removals, below). Combined
with the other decisions published
separately from this CNOR for
individual species that previously were
candidates, a total of 249 species
(including 110 plant and 139 animal
species) are now candidates awaiting
preparation of rules proposing their
listing. These 249 species, along with
the 56 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 five
species identified in the previous CNOR
as either proposed for listing or
classified as candidates that are no
longer in those categories. This includes
one species for which we published a
final rule to list, plus the four species
that we have determined do not warrant
preparation of a rule to propose listing
and therefore have been removed from
candidate status in this CNOR.
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New Candidates
Below we present a brief summary of
one new mammal, one new fish, one
new mussel, 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 Internet website
(https://endangered.fws.gov/candidates/
index.html). 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 three other species, yellowbilled loon, roundtail chub (Lower
Colorado River Basin population), and
Astragalus anserinus (Goose Creek
milkvetch) were identified as candidates
earlier this year as a result of a separate
petition findings published in the
Federal Register.
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Mammals
Florida bonneted bat (Eumops
floridanus) – The following summary is
based on information in our files.
Endemic to south Florida, this species is
known to occur at 12 locations, 5 on
private land and 7 on public land. The
entire population may number less than
a few hundred individuals. Recent
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).
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 because the
locations of any such sites are unknown.
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, distance between
occupied locations, and small number
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of occupied locations. Such factors may
make recolonization unlikely if any site
is extirpated and 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
and insect abundance, and disruption of
the maternal period. 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.
Birds
Yellow-billed loon (Gavia adamsii) –
We previously announced candidate
status for this species in a separate
warranted-but-precluded 12–month
petition finding published on March 25,
2009 (74 FR 12931). Also, see summary
below under ‘‘Petition Findings.’’
Fishes
Roundtail chub (Lower Colorado
River Basin DPS) (Gila robusta) – We
previously announced candidate status
for this species in a separate warrantedbut-precluded 12–month petition
finding published on July 7, 2009 (74 FR
32351).
Diamond darter (Crystallaria cincotta)
– The following summary is based on
information contained in our files. The
diamond darter is a member of the
Perch family (Percidae) that is generally
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translucent with silvery white on the
ventral side of the body and head and
has four wide olive-brown saddles on
the back and upper side. The fish
generally grows to between 73 to 77.3
millimeters (2.9 – 3.0 inches) in
standard length. The species is a benthic
invertivore (feeds on invertebrates) that
inhabits moderate to large warm-water
streams with moderate current and
clean sand and gravel substrates.
Historical records indicate that the
diamond darter was distributed
throughout the Ohio River Basin and
that the range included the Muskingum
River, Ohio; the Ohio River, Ohio; the
Green River, Kentucky; and the
Cumberland River Drainage, Kentucky
and Tennessee. The species is currently
only known to exist within a 36kilometer (km) (22.4-mile (mi)) section
of the lower Elk River in Kanawha and
Clay Counties, West Virginia, and is
considered extirpated from the
remainder of the Ohio River Basin.
Survey results and independent
publications indicate that the diamond
darter is very rare and that the
remaining population within the Elk
River is likely very small. Despite
repeated and targeted survey efforts
within the species’ known range and
preferred habitat in the Elk River, only
18 individuals have been collected in
the last 29 years.
The primary threats to the diamond
darter are related to the present or
threatened destruction, modification, or
curtailment of its habitat or range. The
Elk River Watershed is threatened with
ongoing water-quality degradation and
habitat loss from activities such as coal
mining, oil and gas development,
siltation from these and other sources,
and inadequate sewage and wastewater
treatment. The impoundment of rivers
in the Ohio River Basin, such as the
Kanawha, Ohio, and Cumberland, has
eliminated much of the species’ habitat
and isolated the existing population
from other watersheds that the species
historically occupied. Invasive species
have the potential to affect the Elk River
and diamond darter habitat. The small
size and restricted range of the
remaining diamond darter population
make it particularly susceptible to the
effects of genetic inbreeding, as well as
potential extirpation from spills and
other catastrophic events. The species is
vulnerable to overutilization for
scientific purposes; however, the
significance of this threat has been
reduced and can be further minimized
through the administration of existing
scientific collecting permit procedures.
Existing Federal and State regulatory
mechanisms do not currently provide
protections for the species or its habitat.
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The threats to the diamond darter are
high in magnitude, in that the entire
current range of the species is
potentially affected, and the effects of
the threats severely affect the
reproductive capacity and can result in
total mortality. The threats to the
species are imminent and ongoing.
Activities that pose a threat to the
species already exist within the
watershed and are expected to continue.
Based on imminent threats of a high
magnitude, we assigned an LPN of 2 to
this species.
Clams
Rabbitsfoot (Quadrula cylindrica
cylindrical) – The following summary is
based on information in our files. The
rabbitsfoot is a freshwater mussel native
to Alabama, Arkansas, Georgia, Illinois,
Indiana, Kansas, Kentucky, Louisiana,
Mississippi, Missouri, Ohio, Oklahoma,
Pennsylvania, Tennessee, and West
Virginia. The species has disappeared
from 5 of 6 rivers in the Lower Great
Lakes sub-basin, 47 of 64 rivers in the
Ohio River system, 10 of 12 rivers in the
Cumberland River basin, 14 of 19 rivers
in the Tennessee River system, 2 of 5
rivers in the Lower Mississippi River
sub-basin, 3 of 12 rivers in the White
River system, 4 of 8 rivers in the
Arkansas River system, and 4 of 11
rivers in the Red River system,
representing approximately a 65-percent
decline of its range. Total range
reduction (river miles) and overall
population loss for the rabbitsfoot may
approach, if not exceed, 90 percent. Of
the 49 extant populations, 10
populations are considered to be viable
in the longterm.
Population declines continue in most
of the species’ range, and numerous
threats, including water-quality
degradation, loss of stable substrates,
sedimentation, channelization, gravel
mining, dredging, and impoundments,
are affecting the few remaining
sustainable extant populations. The
small size of most of the remaining
rabbitsfoot populations exacerbates the
threats and adverse effects of chance
events to rabbitsfoot.
Threats to the continued existence of
rabbitsfoot include exotic species,
especially zebra mussels; delivery and
deposition of fine sediments; small
population sizes; isolation of
populations; livestock grazing;
wastewater effluents; mine runoff;
unstable and coldwater flows
downstream of dams; gravel mining;
and channel dredging. In addition, the
rabbitsfoot, like many other fresh-water
mussels, requires a fish host to transport
it larvae, and the fish host of rabbitsfoot
is unknown for the eastern portion of its
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range; thus, artificial propagation of the
rabbitsfoot to reestablish the species in
restored habitats and to maintain nonreproducing populations is not possible,
nor is focused conservation of its fish
host. Although there are ongoing
attempts to alleviate some of these
threats at some locations, there appear
to be no populations without significant
threats and many threats are without
obvious or readily available solutions.
The threats described above have led to
the species being intrinsically
vulnerable to extirpation.
Due to the number of extant
populations and relatively broad
distribution, the threats to rabbitsfoot
are of moderate magnitude. Although
some of the threats are nonimminent,
most are ongoing and, therefore, overall,
the threats are imminent. Thus, we
assigned an LPN of 9 to this subspecies.
Flowering Plants
Astragalus anserinus (Goose Creek
milkvetch) – We previously announced
candidate status for this species in a
separate warranted-but-precluded 12–
month petition finding published on
September 10, 2009 (74 FR 46521).
Leavenworthia exigua var. laciniata
(Kentucky gladecress) – The following
summary is based on information in our
files. Kentucky gladecress is a winter
annual that is adapted to environments
with shallow soils interspersed with
flat-bedded limestones. The natural
habitat for Kentucky gladecress is cedar
glades, but the variety is also known
from overgrazed pastures, eroded
shallow-soil areas with exposed
bedrock, and areas where the soil has
been scraped off the underlying
bedrock. The variety does not appear to
compete well with other vegetation and
is shade intolerant. Currently, there are
approximately 55 occurrences in
Jefferson and Bullitt Counties,
Kentucky, but at least 39 of these
occurrences are of poor quality with low
numbers of plants and degraded
conditions.
Populations of this variety are now
located primarily in modified habitats
such as pastureland, roadside rights of
way, and cultivated or plowed fields.
These populations are threatened by
further habitat destruction (conversion
from rural to residential land use),
herbicide use, overgrazing, and
competition. Some populations
continue to occupy natural glade
habitats, but these habitats are remnant
in nature and continue to be affected by
agricultural and residential conversion.
The variety’s primary threat, habitat
destruction due to residential and
commercial development, is widespread
and has the potential to affect the entire
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range of the variety. The effects of the
threat are also permanent. Therefore,
these threats are high in magnitude.
These threats are imminent because the
conversion from rural to residential land
use is ongoing. Consequently, we
assigned an LPN of 3 to this plant
variety.
Ferns and Allies
Trichomanes punctatum ssp.
floridanum (Florida bristle fern) – The
following summary is based on
information in our files. The Florida
bristle fern has been reduced to four, or
possibly five, small, isolated
occurrences: Three occur in MiamiDade County and two in Sumter County.
In Miami-Dade County, it has been
found exclusively in solution holes in
oolitic limestone and rocky outcrops in
rockland hammocks. In Sumter County,
plants occur in a mesic/hydric
hammock on shaded limestone
boulders.
Most sites where Florida bristle fern
once occurred in Miami-Dade County
have been lost; few rockland hammocks
remains outside of Everglades National
Park. Impacts from regional water
drainage in Miami-Dade County are
severe, and currently occurring.
Regional drainage in remaining habitat
has probably been a stressor that has
contributed to extirpations and
population declines. Resulting drops in
ambient humidity in the habitat may
limit reproduction and health of
populations over the longterm. Such
changes in humidity may cause
extirpations or make plants more
vulnerable to other stressors (e.g.,
periodic long-term droughts,
hurricanes). Climatic changes and sealevel rise are future, long term threats
that are expected to affect habitat and
ultimately reduce the extent of available
habitat in Miami-Dade County.
Agricultural conversion and
development are currently occurring in
Sumter County, placing any
undocumented occurrences and suitable
habitat at risk. Since a full survey of
suitable habitats for the Florida bristle
fern has never been conducted in
Sumter County, we cannot determine
the full extent of losses of this species
due to habitat destruction and
modification. All known extant
occurrences are located on conservation
lands; however, there is potential,
especially in Sumter County, for the
species to occur on private lands.
Together, the extant occurrences contain
fewer than 1,000 plants. Many plants
are probably clones, so there may be
limited genetic diversity within sites.
Because there are few occurrences,
populations contain few plants, and
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genetic variability is low, the species is
inherently at risk due to stochastic
events. Droughts, tropical storms, and
hurricanes are threats; Hurricane
Andrew may have played a role in the
extirpation of the species from two sites.
Since there are few occurrences
remaining, the species is threatened
with extinction during these events.
Invasive exotic plants are also a threat,
but may be reduced due to active
programs by Miami-Dade County and
the State. The extent to which fungus is
a threat to wild populations is
unknown. Overall, the magnitude of
threats is high, and most threats are
occurring and are, therefore, imminent.
Consequently, we assigned this
subspecies an LPN of 3.
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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 imminence 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.
Birds
Elfin-woods warbler (Dendroica
angelae) – The 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 highelevation dwarf or elfin forests of Puerto
Rico, 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, Sierra
de Cayey, and the Commonwealth
forests of Maricao and Toro Negro.
However, it has not been recorded again
in Toro Negro and Cayey since 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
Forest, Guilarte Forest, Bosque del
Pueblo, Maricao Forest and the El
Yunque National Forest (Luquillo
Mountains), but the species was
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detected only in the latter two. In the
Maricao Commonwealth Forest, 778
elfin-woods warblers were recorded,
and in the El Yunque National Forest,
196 were recorded.
The elfin-woods warbler is threatened
by habitat modification. Destruction of
elfin forest and Podocarpus forest by the
installation of infrastructure
(telecommunication towers and
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
Department of Natural and
Environmental Resources potentially
installing these structures. Furthermore,
restoration of this habitat would take a
few 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 shadecoffee plantations) along the periphery
of the Maricao Commonwealth Forest to
marginal habitat (e.g., pastures, dry
slope forests, residential rural forests,
gallery forests, and sun-coffee
plantations) may result in ineffective
corridors for dispersal and expansion of
the elfin-woods warbler. Although 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. We previously
assessed the LPN as a 5 (high
magnitude, nonimminent threats). 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 the species 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, we have determined that the
magnitude of threats is moderate to low
because the severity of the threats on the
species is not as great as we previously
believed and most of the range of the
elfin-woods warbler is within protected
lands. The threats are not currently
occurring in most of the warbler’s
habitat; therefore, the threats are
nonimminent. As a result, we have
changed the LPN from a 5 to an 11 for
this species.
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Fish
Pearl darter (Percina aurora) – Little
is known about the specific habitat
requirements or natural history of the
Pearl darter. Pearl darters have been
collected from rivers and streams with
a variety of attributes, but are mainly
found 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 reductions casused
by 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 and would also make this
species more vulnerable to catastrophic
events. Reevaluation of the threats
affecting the pearl darter has indicated
that a change in the Listing Priority
Number is warranted. Threats affecting
the pearl darter are localized in nature,
affecting portions of the population
within the drainage. Thus, a threat
magnitude of moderate to low is a more
appropriate category in this situation. In
addition, since the identified threats are
currently affecting this species in these
portions of its range, the threats are
imminent. Therefore, we have changed
the LPN from a 5 to an 8 to reflect this
reevaluation.
Clams
Neosho mucket (Lampsilis
rafinesqueana) – 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) of its range, primarily 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 historical
range have been inundated by the
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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 to
this river. The rapid collapse of the
entire mussel community, including
Neosho mucket, since 2005 in the
Arkansas portion of the Illinois River
threatens to extirpate the species from
approximately 30 river miles 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 because of their severity on
this species, and they occur throughout
the range. The majority of the threats are
ongoing and thus imminent. Thus, we
changed the LPN from a 5 to a 2 for this
species.
Insects
Miami blue butterfly (Cyclargus
thomasi bethunebakeri) – The Miami
blue is endemic to south Florida.
Historically, it occurred throughout the
Florida Keys, 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
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early successional habitats such as the
edges of tropical hardwood hammock,
coastal berm forest, and along trails and
other open sunny areas, and historically
in pine rocklands. These habitats
provide host plants 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
hostplants from iguanas at BHSP is a
new, ongoing, significant threat;
although active steps are being taken by
the State, 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,
mosquito control, and accidental harm
from humans; increasing the current
population in size; and establishing
populations at other locations. The
threats are high in magnitude and
constitute a significant risk to the
subspecies. Given that the new threat
from iguanas and other threats
(hurricanes, few occurrences, and small
population size) are ongoing, the threats
are imminent. Therefore, we changed
the LPN from a 6 to a 3.
Flowering plants
Helianthus verticillatus (whorled
sunflower) – 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
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57809
usage in association with right-of-way
maintenance. The majority of the
Georgia population is protected due to
its location within a conservation
easement area; 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
habitat, the other Alabama population
has responded favorably to canopy
removal that took place circa 2001.
Because of this, the threats are of
moderate magnitude. The threats are
currently occurring, and therefore
imminent. To help ensure consistency
in the application of our listing priority
process, we changed the LPN from a 5
to an 8 for this species.
Lesquerella globosa (Short’s
bladderpod) – 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; talus areas, along cliff
tops and bases; and on cliff ledges. It is
usually associated with south-to-westfacing 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
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
many locations, active habitat
management is necessary at those sites.
The threats from roadside maintenance
and habitat alterations by invasive plant
encroachment are moderate in
magnitude, as they are not affecting all
locations of this species. However, the
threats are currently occurring, and
therefore imminent. To help ensure
consistency in the application of our
listing priority process, we changed the
LPN from a 5 to an 8 for this species.
Physaria douglasii ssp. tuplashensis
(White Bluffs bladderpod) – In previous
Candidate Notices of Review, we
referred to P. douglasii ssp. tuplashensis
as P. tuplashensis. We have now
dropped that name because the paper
that recommended its use was never
published. As a result, we are following
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the treatment of a 2002 published
scientific paper that recognized the
White Bluffs bladderpod as Physaria
douglassii ssp. tuplashensis.
White Bluffs bladderpod is a lowgrowing, herbaceous, short-lived
perennial plant in the Brassicaceae
(mustard) family. Historically and
currently, White Bluffs bladderpod (P.
douglasii ssp. tuplashensis) has been
known from only 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
33 feet (10 meters) wide by 10.6 miles
(17 km) 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. However, the
southern portion 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
destroy plants, and the presence of
invasive nonnative plants that compete
with P. douglassii ssp. 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 ssp.
tuplashensis population. As a result of
a fire in 2007, there is a higher
probability that invasion of these
nonnatives will occur. We reanalyzed
the magnitude and imminence of the
threats, which resulted in a change in
the LPN for P. douglasii ssp.
tuplashensis. 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 and 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 relatively
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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 85 percent having Federal
ownership. Even though off-road
vehicle use is prohibited on the
monument, intermittent, ongoing use
does occur. However, these activities,
although they are ongoing, are mainly
confined to the upper portion of the
White Bluffs where few P. 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
described as a significant problem.
While P. douglasii ssp. tuplashensis is
inherently vulnerable because it is a
narrow endemic, the magnitude of the
threats to the population is moderate.
The threats are currently occurring, and
therefore imminent. To help ensure
consistency in the application of our
listing priority process and to recognize
the correct taxonomic name, we
changed the LPN from a 5 to a 9 for this
subspecies.
Platanthera integrilabia (White
fringeless orchid) – Platanthera
integrilabia is a perennial herb that
grows in partially but not fully shaded,
wet, boggy areas at the heads of streams
and on seepage slopes in Alabama,
Georgia, Kentucky, and Tennessee.
Historically, there were at least 90
populations of P. integrilabia. Currently
there are approximately 50 extant sites
supporting the species.
Several populations have been
extirpated due to road, residential, and
commercial construction and 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 that the
hydrology of the bogs that support the
species is not altered. Natural
succession can result in decreased light
levels. Because of the species’
dependence upon moderate to high light
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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 by
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
threaten several sites. Upon review of
current listing guidance and threats
affecting the species, we have revised
the LPN to reflect the fact that threats
are currently operating at most sites and
are therefore imminent. While 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 the threats by being
within State parks, national forests,
wildlife management areas, or other
protected land. As a result, we changed
the LPN from a 5 to an 8 for this species.
Candidate Removals
As summarized below, we have
evaluated the threats to the following
four species and considered factors that,
individually and in combination,
currently or potentially could pose a
risk to these species and their habitat.
After a review of the best available
scientific and commercial data, we
conclude that listing these four species
under the Endangered Species Act is not
warranted because the species are not
likely to become endangered species
within the foreseeable future throughout
all or a significant portion of their range.
Therefore, for each of these species 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
these species, and to accept additional
information and comments concerning
this finding. We will reconsider our
determination for each species in the
event that new information indicates
that the threats to the species are of a
considerably greater magnitude or
imminence than identified through
assessments of information contained in
our files, as summarized here.
Snails
Fat-whorled pondsnail (Stagnicola
bonnevillenis) – The fat-whorled
pondsnail, also known as the Bonneville
pondsnail, was thought to occur in only
four spring pools north of the Great Salt
Lake in Box Elder County, Utah.
Additional surveys found Lymnaeid
snails including S. bonnevillensis-like
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shells in springs throughout the playa.
New information shows that shell
characteristics vary greatly with
environmental conditions. Because the
fat-whorled pondsnail was classified
based only on the shell appearance, the
taxonomy is questionable. Because of
uncertainties surrounding the validity of
S. bonnevillensis as a species, we
evaluated all Stagnicola sp. inhabiting
the spring pools previously thought to
be occupied by S. bonnevillensis. The
primary threat to these pools has been
chemical contamination of the
groundwater. Significant actions have
been taken to remediate this threat,
including implementing corrective
actions to track and remediate
groundwater contamination,
implementation of a site management
plan, and development of a groundwater
model and risk assessment. The plan
has been implemented, and
conservation measures are currently
being monitored for effectiveness. These
efforts have been under way for a
sufficient period to effectively eliminate
the threat from contamination. We know
of no other threats to the springs in the
range of S. bonnevillensis. Based on
findings and analysis in our updated
assessment, we conclude that this
species in not likely to become an
endangered species within the
foreseeable future throughout all or a
significant portion of its range, and
listing this species under the
Endangered Species Act is therefore not
warranted. The species no longer meets
our definition of a candidate, and we
have removed it from candidate status.
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Crustaceans
Troglobitic groundwater shrimp
(Typhlatya monae) – Typhlatya monae
is a small subterranean small shrimp
known from Puerto Rico, Barbuda, and
the Dominican Republic. It is classified
as a troglobite, or obligatory cave
organism, of which its most
extraordinary feature is the reduction or
loss of vision and pigmentation. T.
monae feeds on organic waste material
and debris, such as bat guano. Little is
known concerning the status of T.
monae in either Barbuda or Dominican
Republic and we are not aware of any
threats to this species in those locations.
This species was discovered on Mona
Island, in Puerto Rico but was later
found on the Puerto Rico mainland in
´
three caves within the Guanica
Commonwealth Forest in the
´
municipalities of Guanica, Yauco, and
Guayanilla. Although the species was
not found on Mona Island during
surveys conducted in 1974 and 1995,
the species may still be found in the reef
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deposit aquifers in Mona Island that
have not yet been surveyed.
In 1995, the total population was
estimated to be close to 2,000
individuals; over 95 percent of these
were observed in one cave. Although no
systematic censuses have been
conducted since 1995, the Service has
recently documented the presence of the
species in all three mainland caves and
obtained information from Puerto Rico
Commonwealth Forest personnel
regarding two additional caves in which
the species may occur.
In past reviews, we determined that
the species was threatened by habitat
disturbance, human-induced fires,
hurricanes and floods. However, the
´
Guanica Commonwealth Forest and
Mona Island Natural Reserve are
managed for conservation by the Puerto
Rico Department of Natural and
Environmental Resources (DNER). Caves
´
in the Guanica Forest are closed to
public visitors; therefore, habitat
modification and disturbance, and
human-induced fires are not
anticipated. Caves on Mona Island are
seldom visited, and adverse effects to
these areas have not been documented.
The species is located in pools inside
caves, and underground waters; thus,
we do not anticipate impacts from
hurricanes. Typhlatya monae was first
described in Mona Island from el Pozo
Del Portuguez and from a deep well
close to the airport. At the present time,
the use of this well is limited to DNER
staff; therefore, additional extraction of
underground waters is not expected.
Currently, the DNER utilizes water
cisterns and commercial potable water
as alternate water sources. The species
is protected by Regulation #6766
(‘‘Reglamento para Regir las Especies
¨
Vulnerables y en Peligro de Extincion
en el Estado Libre Asociado de Puerto
Rico’’), adopted in 2004 by the
Commonwealth of Puerto Rico. Under
Regulation #6766, T. monae is listed as
Critically Endangered (CR). Regulation
#6766 prohibits collecting, killing, or
harming listed species. We conclude
that this species in not likely to become
an endangered species within the
foreseeable future throughout all or a
significant portion of its range, and
listing this species under the
Endangered Species Act is not
warranted. The species no longer meets
our definition of a candidate, and we
have removed it from candidate status.
Flowering Plants
Calliandra locoensis (no common
name) – Calliandra locoensis is a spiny,
leguminous shrub currently known from
´
five localities within the Susua
Commonwealth Forest in the
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57811
municipalities of Yauco and Sabana
Grande, in southwestern Puerto Rico.
This species is endemic to Puerto Rico,
and was discovered in 1991 during a
´
study of the flora of the Susua
Commonwealth Forest; it was described
´
by Garcia and Kolterman in 1992.
Calliandra locoensis is found on
shallow, serpentine soils with low
nutrients, high drainage, and low
fertility. In 2007, local botanists
reported 3 populations with
approximately 1,600 adult plants and
numerous seedlings in 5 localities
indicating that the number of adult
individuals has doubled and the
number of localities has increased since
surveys conducted in 1998.
In previous reviews, we determined
that the species was threatened by
forest-management practices (accidental
trampling, brush clearing, trail
maintenance), forest fires (natural or
manmade), catastrophic natural events
(hurricanes, floods, mudslides), and
restricted distribution. We now find that
this species is not currently threatened
by forest management practices. The
species is currently considered as a
critical element under the Puerto Rico
Department of Natural and
Environmental Resources Natural
Heritage Program; consequently
activities conducted in the forest are
generally scrutinized and measures to
minimize or avoid impacts to species
are recommended and implemented.
´
The Susua Commonwealth Forest is also
protected by Law #133 and has been
designated as a Critical Wildlife Area.
We also previously indicated that this
species was vulnerable to hurricanes
and human-induced fires. Plants
endemic to the Caribbean are naturally
adapted to the impact of hurricanes (the
species usually lose their leaves for a
certain period of time, but recover them
later). Although hurricanes are common
occurrences in Puerto Rico, damage to
this species by hurricanes has not been
reported in any of the currently known
populations in the last decade. Surveys
have indicated that despite hurricanes
occurring in the areas where C.
locoensis exists, the number of adult
individuals has doubled, the number of
localities has increased, evidence
suggests that the species is successfully
reproducing. Thus, we have determined
that hurricanes are not a threat. The
currently known populations are not
located near the roads of the forest,
which are more vulnerable to fires and
DNER implements a fire prevention
plan within the forest, particularly
during the dry season; therefore, fire is
not a threat to the species. We conclude
that this species in not likely to become
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an endangered species within the
foreseeable future throughout all or a
significant portion of its range, and
listing this species under the
Endangered Species Act is not
warranted. The species no longer meets
our definition of a candidate, and we
have removed it from candidate status.
Calyptranthes estremerae (no
common name) – Calyptranthes
estremerae is a small tree from the
subtropical moist forest of northwestern
Puerto Rico, in the municipalities of
Camuy, Utuado, and Arecibo.
Calyptranthes estremerae was only
known from several individuals found
near the recreation area adjacent to the
´
Rio Camuy Cave Park. At present time,
about 100 individuals of C. estremerae
are estimated for the Camuy Cave Park
´
area, Rio Abajo Commonwealth Forest
(managed by the Puerto Rico
Department of Natural and
Environmental Resources (DNER)), and
a privately owned farm in Sabana
Hoyos, Arecibo.
We have found that this species is no
longer threatened by the expansion of
recreation facilities within Cavernas de
´
Camuy Park and Rio Abajo
Commonwealth Forest, as there are no
plans to expand such facilities. In
´
addition, the Rio Abajo Commonwealth
Forest has a management plan in place
that emphasizes protection and
conservation of species classified under
DNER as critical, threatened, or
endangered and their habitat; C.
estremerae is classified as a critical
element by DNER. Furthermore, actions
that may affect such classified species
are generally scrutinized, and measures
to minimize or avoid impacts to these
species are recommended and
´
implemented. The Rio Abajo
Commonwealth Forest is also protected
by designation as a Critical Wildlife
Area. In previous assessments, we
indicated that the small number of
individuals of C. estremerae in the two
populations, along with the species’
limited distribution made this species
vulnerable to potential catastrophic
natural (hurricanes) and manmade
(fires) events. However, damage by
hurricanes has not been reported in any
of the currently known populations. In
addition, because the species exists in
the subtropical moist forest life zone,
the threat of human-induced fires is
low; further, the DNER implements an
islandwide fire prevention plan in
public forests. Therefore, fires are
currently not a threat to this species. We
conclude that this species in not likely
to become an endangered species within
the foreseeable future throughout all or
a significant portion of its range, and
listing this species under the
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Endangered Species Act is not
warranted. The species 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.
Under section 4(b)(3)(A), when we
receive such a petition, we must
determine within 90 days, to the
maximum extent practicable, whether
the petition presents substantial
information 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
regulation implementing the petitioned
action is precluded by pending
proposals, and (b) expeditious progress
is being made to add qualified species
to the lists of endangered or threatened
species. (We refer to this as a
‘‘warranted-but-precluded finding.’’)
Section 4(b)(3)(C) 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 are required to
publish new 12–month findings on
these ‘‘resubmitted’’ petitions on an
annual basis.
On December 5, 1996, we made a final
decision to redefine ‘‘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,
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1996). Therefore, the standard for
making a species a candidate through
our own initiative is identical to the
standard for making a warranted-butprecluded 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.
This publication provides notice of
substantial 90–day findings and the
warranted-but-precluded 12–month
findings pursuant to section 4(b)(3) for
candidate species listed on Table 1 that
we identified on our own initiative, and
that subsequently have been the subject
of a petition to list. Even though all
candidate species identified through our
own initiative already have received the
equivalent of substantial 90–day and
warranted-but-precluded 12–month
findings, 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.
Pursuant to section 4(b)(3)(C)(i) of the
Act, once a petition is filed regarding a
candidate species, 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 notwarranted finding. We make these
annual findings for petitioned candidate
species through the CNOR.
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, whether it was identified
through our own initiative or through
the petition process, we will make
prompt use of the emergency listing
authority under section 4(b)(7). We have
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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).
On June 20, 2001, the United States
Court of Appeals for the Ninth Circuit
held that the 1999 CNOR (64 FR 57534;
October 25, 1999) did not demonstrate
that we fulfilled the second component
of the warranted-but-precluded 12–
month petition findings for the Gila
chub and Chiracahua leopard frog
(Center for Biological Diversity v.
Norton, 254 F.3d 833 (9th Cir. 2001)).
The court found that the one-line
designation in the table of candidates in
the 1999 CNOR, with no further
explanation, did not satisfy section
4(b)(3)(B)(iii)’s requirement that the
Service publish a finding ‘‘together with
a description and evaluation of the
reasons and data on which the finding
is based.’’ The court suggested that this
one-line statement of candidate status
also precluded meaningful judicial
review.
On June 21, 2004, the United States
District Court for Oregon agreed that we
can use the CNOR as a vehicle for
making petition findings and that our
reasoning for why listing is precluded
does not need to be based on an
assessment at a regional level (as
opposed to a national level) (Center for
Biological Diversity v. Norton Civ. No.
03-1111-AA (D. Or.)). However, this
court found that our discussion on why
listing the candidate species were
precluded by other actions lacked
specificity; in the list of species that
were the subject of listing actions that
precluded us from proposing to list
candidate species, we did not state the
specific action at issue for each species
in the list and we did not indicate
which actions were court-ordered.
On June 22, 2004, in a similar case,
the United States District Court for the
Eastern District of California also
concluded that our determination of
preclusion may appropriately be based
on a national analysis (Center for
Biological Diversity v. Norton No. CV S03-1758 GEB/DAD (E.D. Cal.)). This
court also found that the Act’s
imperative that listing decisions be
based solely on science applies only to
the determination about whether listing
is warranted, not the question of when
listing is precluded.
On March 24, 2005, the United States
District Court for the District of
Columbia held that we may not consider
critical habitat activities in justifying
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our inability to list candidate species,
requiring that we justify both our
preclusion findings and our
demonstration of expeditious progress
by reference to listing proceedings for
unlisted species (California Native Plant
Society v. Norton, Civ. No. 03-1540 (JR)
(D.D.C.)). The court further found that
we must adequately itemize priority
listings, explain why certain species are
of high priority, and explain why
actions on these high-priority species
preclude listing species of lower
priority. The court approved our
reliance on national rather than regional
priorities and workload in establishing
preclusion and approved our basic
explanation that listing candidate
species may be precluded by statutorily
mandated deadlines, court-ordered
actions, higher priority listing activities,
and a limited budget.
In this CNOR we continue to
incorporate information that addresses
the courts’ concerns. 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, 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
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57813
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 162
candidates and 6 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 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.
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. 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, 2008, through
September 30, 2009. 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
these particular candidates warrant
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 website: https://
endangered.fws.gov/. 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
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of species determined to be 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 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
competing demands for those resources.
Thus, in any given fiscal year (FY),
multiple factors dictate whether it will
be possible to undertake work on a
proposed listing regulation or whether
promulgation of such a proposal is
warranted but precluded by higher
priority listing actions.
The resources available for listing
actions are determined through the
annual Congressional appropriations
process. The appropriation for the
Listing Program is available to support
work involving the following listing
actions: proposed and final listing rules;
90–day and 12–month findings on
petitions to add species to the Lists of
Endangered and Threatened Wildlife
and Plants (Lists) or to change the status
of a species from threatened to
endangered; annual determinations on
prior warranted-but-precluded petition
findings as required under section
4(b)(3)(C)(i) of the Act; 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. For example, during the
past several years, the cost (excluding
publication costs) for preparing a 12–
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month finding, without a proposed rule,
has ranged from approximately $11,000
for one species with a restricted range
that requires a relatively uncomplicated
analysis to $305,000 for another species
that is wide-ranging and requires a
complex analysis.
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).
Recognizing that designation of
critical habitat for species already listed
would consume most of the overall
Listing Program appropriation, Congress
also put a critical habitat subcap in
place in FY 2002, and has retained it
each subsequent year to ensure that
some funds are available for other work
in the Listing Program: ‘‘The critical
habitat designation subcap will ensure
that some funding is available to
address other listing activities’’ (House
Report No. 107 - 103, 107th Congress, 1st
Session, June 19, 2001). In FY 2002 and
each year until FY 2006, the Service has
had to use virtually the entire critical
habitat subcap to address courtmandated designations of critical
habitat, and consequently none of the
critical habitat subcap funds have been
available for other listing activities. In
FY 2007, we were able to use some of
the critical habitat subcap funds to fund
proposed listing determinations for
high-priority candidate species;
however, in subsequent FYs we were
unable to do this because all of the
critical habitat subcap funds were
needed to address our workload for
designating critical habitat.
Thus, through the listing cap, the
critical habitat subcap, and the amount
of funds needed to address courtmandated critical habitat designations,
Congress and the courts have in effect
determined the amount of money
available for other listing activities.
Therefore, the funds in the listing cap,
other than those needed to address
court-mandated critical habitat for
already listed species, represent the
resources we must take into
consideration when we make our
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determinations of preclusion and
expeditious progress.
Congress also recognized that the
availability of resources was the key
element in deciding, when making a 12–
month petition finding, whether we
would prepare and issue a listing
proposal or instead make a warrantedbut-precluded finding for a given
species. The Conference Report
accompanying Pub. L. 97-304, which
established the current statutory
deadlines and the warranted-butprecluded finding, states (in a
discussion on 90–day petition findings
that by its own terms also covers 12–
month findings) that the deadlines were
‘‘not intended to allow the Secretary to
delay commencing the rulemaking
process for any reason other than that
the existence of pending or imminent
proposals to list species subject to a
greater degree of threat would make
allocation of resources to such a petition
[that is, for a lower-ranking species]
unwise.’’
In FY 2009, expeditious progress is
that amount of work that can be
achieved with $8,808,000, which is the
amount of money that Congress
appropriated for the Listing Program
(that is, the portion of the Listing
Program funding not related to critical
habitat designations for species that are
already listed). Our process is to make
our determinations of preclusion on a
nationwide basis to ensure that the
species most in need of listing will be
addressed first and also because we
allocate our listing budget on a
nationwide basis. The $8,808,000 was
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 litigationrelated, administrative, and listing
program-management functions; and
high-priority listing actions for some of
our candidate species. The allocations
for each specific listing action are
identified in the Service’s FY 2009
Allocation Table (part of our
administrative record).
In FY 2007, we had more than 120
species with an LPN of 2, based on our
September 21, 1983, guidance for
assigning an LPN for each candidate
species (48 FR 43098). Using this
guidance, we assign each candidate an
LPN of 1 to 12, depending on the
magnitude of threats (high vs. moderate
to low), immediacy of threats (imminent
or nonimminent), and taxonomic status
of the species (in order of priority:
monotypic genus (a species that is the
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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
high-priority species, we further ranked
the candidate species with an LPN of 2
by using the following extinction-risk
type criteria: International Union for the
Conservation of Nature and Natural
Resources (IUCN) Red list status/rank,
Heritage rank (provided by
NatureServe), Heritage threat rank
(provided by NatureServe), and species
currently with fewer than 50
individuals, or 4 or fewer populations.
Those species with the highest IUCN
rank (critically endangered), the highest
Heritage rank (G1), the highest Heritage
threat rank (substantial, imminent
threats), and currently with fewer than
50 individuals, or fewer than 4
populations, comprised a 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 on proposed
and final listing rules for these 40
candidates, we are applying the ranking
criteria to the next group of candidates
with LPN of 2 and 3 to determine the
next set of highest priority candidate
species.
To be more efficient in our listing
process, as we work on proposed rules
for these species in the next several
years, we are preparing multi-species
proposals when appropriate, and these
may include species with lower priority
if they overlap geographically or have
the same threats as a species with an
LPN of 2. In addition, available staff
resources are also a factor in
determining which high-priority species
will receive funding. Finally, proposed
rules for reclassification of threatened
species to endangered are lower
priority, since as listed species, they are
already afforded the protection of the
Act and implementing regulations.
Thus, we continue to find that
proposals to list the petitioned
candidate species included in Table 1
are all warranted but precluded.
57815
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. (Although we do
not discuss it in detail here, we are also
making expeditious progress in
removing species from the list under the
Recovery program, which is funded by
a separate line item in the budget of the
Endangered Species Program. As
explained above in our description of
the statutory cap on Listing Program
funds, the Recovery Program funds and
actions supported by them cannot be
considered in determining expeditious
progress made in the Listing Program.)
As with our ‘‘precluded’’ finding,
expeditious progress in adding qualified
species to the Lists is a function of the
resources available and the competing
demands for those funds. Given that
limitation, we find that we made
expeditious progress in FY 2009 in the
Listing Program. This progress included
preparing and publishing the following
determinations:
FY 2009 COMPLETED LISTING ACTIONS
Publication Date
Title
Actions
FR Pages
90-Day Finding on a Petition To List the Least Chub
Notice of 90–day Petition
Finding, Substantial
73 FR 61007 61015
10/21/2008
Listing 48 Species on Kauai as Endangered and Designating
Critical Habitat
Proposed Listing,
Endangered; Proposed
Critical Habitat
73 FR 62591 62742
10/24/2008
90-Day Finding on a Petition to List the Sacramento Valley
Tiger Beetle as Endangered
Notice of 90–day Petition
Finding, Not
substantial
73 FR 63421 63424
10/28/2008
90-Day Finding on a Petition To List the Dusky Tree Vole
(Arborimus longicaudus silvicola) as Threatened or
Endangered
Notice of 90–day Petition
Finding, Substantial
73 FR 63919 63926
11/25/2008
12-Month Finding on a Petition To List the Northern Mexican
Gartersnake (Thamnophis eques megalops) as Threatened
or Endangered With Critical Habitat; Proposed Rule
Notice of 12 month
petition finding,
Warranted but precluded
73 FR 71787 71826
12/02/2008
90-Day Finding on a Petition To List the Black-tailed Prairie
Dog as Threatened or Endangered
Notice of 90–day Petition
Finding, Substantial
73 FR 73211 73219
12/05/2008
90-Day Finding on a Petition To List the Sacramento
Mountains
Checkerspot
Butterfly
(Euphydryas
cloudcrofti) as Endangered with Critical Habitat
Notice of 90–day Petition
Finding, Substantial
73 FR 74123 74129
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90-Day Finding on a Petition to Change the Listing Status of
the Canada Lynx
Notice of 90–day Petition
Finding, Substantial
73 FR 76990 76994
1/06/2009
Partial 90-Day Finding on a Petition To List 475 Species in the
Southwestern United States as Threatened or Endangered
With Critical Habitat
Notice of 90–day Petition
Finding, Not
substantial
74 FR 419 427
2/05/2009
Partial 90-Day Finding on a Petition To List 206 Species in the
in the Midwest and Western United States as Threatened or
Endangered With Critical Habitat
Notice of 90–day Petition
Finding, Not
substantial
74 FR 6122 6128
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FY 2009 COMPLETED LISTING ACTIONS—Continued
Publication Date
Title
Actions
FR Pages
90-Day Finding on a Petition To List the Wyoming Pocket
Gopher as Threatened or Endangered With Critical Habitat
Notice of 90–day Petition
Finding, Substantial
74 FR 6558 6563
3/17/2009
Listing Phyllostegiahispida (No Common Name) as
Endangered Throughout Its Range
Final Listing Endangered
74 FR 11319 11327
3/25/2009
12-Month Finding on a Petition to List the Yellow-Billed Loon
as Threatened or Endangered
Notice of 12 month
petition finding,
Warranted but precluded
74 FR 12931 12968
4/09/2009
12-Month Finding on a Petition to List the San Francisco BayDelta Population of the Longfin Smelt (Spirinchus
thaleichthys) as Endangered
Notice of 12 month
petition finding, Not
warranted
74 FR 16169 16175
4/22/2009
90-Day Finding on a Petition To List the Tehachapi Slender
Salamander (Batrachoseps stebbinsi) as Threatened or
Endangered
Notice of 90–day Petition
Finding, Substantial
74 FR 18336 18341
5/07/2009
90-Day Finding on a Petition To List the American Pika as
Threatened or Endangered with Critical Habitat
Notice of 90–day Petition
Finding, Substantial
74 FR 21301 21310
5/19/2009
12-Month Finding on a Petition to List the Coaster Brook Trout
as Endangered
Notice 12–month petition
finding, Not warranted
74 FR 23376 23388
6/09/2009
90-Day Finding on a Petition To List Oenothera acutissima
(Narrowleaf Evening-primrose) as Threatened or
Endangered
Notice of 90–day Petition
Finding, Not
substantial
74 FR 27266 27271
6/29/2009
Proposed Endangered Status for the Georgia Pigtoe Mussel,
Interrupted Rocksnail, and Rough Hornsnail with Critical
Habitat
Proposed Listing,
Endangered; Proposed
Critical Habitat
74 FR 31113 31151
7/01/2009
90-Day Finding on a Petition to List the Northern Leopard Frog
(Lithobates [=Rana] pipiens) in the Western United States as
Threatened
Notice of 90–day Petition
Finding, Substantial
74 FR 31389 31401
7/07/2009
12-Month Finding on a Petition To List a Distinct Population
Segment of the Roundtail Chub (Gila robusta) in the Lower
Colorado River Basin
Notice of 12–month
petition finding,
Warranted but precluded
74 FR 32351 32387
7/08/2009
90-Day Finding on a Petition to List the Coqui Llanero
(Eleutherodactylus juanariveroi) as Endangered
Notice of 90–day Petition
Finding, Substantial
74 FR 32510 32513
7/08/2009
90-Day Finding on a Petition to List the Susan’s purse-making
caddisfly (Ochrotrichia susanae) as Threatened or
Endangered
Notice of 90–day Petition
Finding, Substantial
74 FR 32514 32521
7/08/2009
Proposed Endangered Status for Flying Earwig Hawaiian
Damselfly (Megalagrion nesiotes) and Pacific Hawaiian
Damselfly (M. pacificum) Throughout Their Ranges
Proposed Listing,
Endangered
74 FR 32490 32510
7/09/2009
Listing Casey’s June Beetle (Dinacoma caseyi) as Endangered
and Designation of Critical Habitat
Proposed Listing,
Endangered; Proposed
Critical Habitat
74 FR 32857 32875
7/22/2009
90-Day Finding on a Petition To List the White-Sided
Jackrabbit (Lepus callotis) as Threatened or Endangered
Notice of 90–day Petition
Finding, Substantial
74 FR 36152 36158
8/06/2009
Initiation of Status Review for Mountain Whitefish (Prosopium
williamsoni) in the Big Lost River, Idaho
Notice of Status Review
74 FR 39268 39269
8/11/2009
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2/10/2009
90-Day Finding on a Petition To List the Jemez Mountains
Salamander (Plethodon neomexicanus) as Threatened or
Endangered With Critical Habitat
Notice of 90–day Petition
Finding, Substantial
74 FR 40132 40138
8/18/2009
Partial 90-Day Finding on a Petition To List 206 Species in the
Midwest and Western United States as Threatened or
Endangered with Critical Habitat
Notice of 90–day Petition
Finding, Not
substantial (9 species);
Notice 90–day Petition
Finding, Substantial
(29 species)
74 FR 41649 41662
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FY 2009 COMPLETED LISTING ACTIONS—Continued
Publication Date
Title
Actions
FR Pages
8/19/2009
12-Month Finding on a Petition To List the Ashy Storm-Petrel
as Threatened or Endangered
Notice of 12 month
petition finding,
Not warranted
74 FR 41832 41860
8/28/2009
90-Day Finding on a Petition To List the Sonoran Population of
Desert Tortoise (Gopherus agasizzii) as a Distinct
Population Segment (DPS) With Critical Habitat
Notice of 90–day Petition
Finding, Substantial
74 FR 44335 44344
9/02/2009
12-Month Finding on a Petition To List the Sacramento
Mountains Checkerspot Butterfly as Endangered with Critical
Habitat
Notice of 12 month
petition finding, Not
warranted
74 FR 45396 45411
9/09/2009
90-Day Finding on a Petition to List the Eastern Population of
the Gopher Tortoise (Gopherus polyphemus) as Threatened
Notice of 90–day Petition
Finding, Substantial
74 FR 46401 46406
9/10/2009
12-Month Finding on a Petition to List Astragalus anserinus
(Goose Creek milkvetch) as Threatened or Endangered
Notice of 12 month
petition finding, Warranted but precluded
74 FR 46521 46542
9/10/2009
90-Day Finding on a Petition to List Cirsium wrightii (Wright’s
marsh thistle) as Threatened or Endangered with Critical
Habitat
Notice of 90–day Petition
Finding, Substantial
74 FR 46542 46547
9/10/2009
90-Day Finding on a Petition to List the Pacific Walrus as
Threatened or Endangered
Notice of 90–day Petition
Finding, Substantial
74 FR 46551 46557
9/10/2009
Endangered and Threatened Wildlife and Plants; 90-Day
Finding on a Petition to List the Amargosa Toad (Bufo nelsoni)
as Threatened or Endangered
Notice of 90–day Petition
Finding, Substantial
74 FR 46548 46551
Our expeditious progress also
included work on listing actions that we
funded in FY 2009 but have not yet
been completed to date. These actions
are listed below. Actions in the top
section of the table are being conducted
under a deadline set by a court. Actions
in the middle section of the table are
being conducted to meet statutory
timelines, that is, timelines required
under the Act. Actions in the bottom
section of the table are high-priority
listing actions. These actions include
work primarily on species with an LPN
of 2, and selection of these species is
partially based on available staff
resources, and when appropriate,
include species with a lower priority if
they overlap geographically or have the
same threats as the species with the
high priority. Including these species
together in the same proposed rule
results in considerable savings in time
and funding as compared to preparing
separate proposed rules for each of them
in the future.
ACTIONS FUNDED IN FY 2009 BUT NOT COMPLETED IN FY 2009
SPECIES
ACTION
ACTIONS SUBJECT TO COURT ORDER/SETTLEMENT AGREEMENT
Final listing determination
Coastal cutthroat trout
Final listing determination
Mono basin sage-grouse
12–month petition finding
Greater sage-grouse
12–month petition finding
SW bald eagle population
12–month petition finding
Black-tailed prairie dog
12–month petition finding
Lynx (include New Mexico in listing)
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Slickspot peppergrass
12–month petition finding
White-tailed prairie dog
12–month petition finding
American pika
12–month petition finding
Hermes copper butterfly
90–day petition finding
Thorne’s hairstreak butterfly
90–day petition finding
ACTIONS WITH STATUTORY DEADLINES
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ACTIONS FUNDED IN FY 2009 BUT NOT COMPLETED IN FY 2009—Continued
SPECIES
ACTION
48 Kauai species
Final listing determination
Black-footed albatross
12–month petition finding
Mount Charleston blue butterfly
12–month petition finding
Mojave fringe-toed lizard1
12–month petition finding
Pygmy rabbit (rangewide)1
12–month petition finding
Kokanee – Lake Sammamish population1
12–month petition finding
Delta smelt (uplisting)
12–month petition finding
Cactus ferruginous pygmy-owl1
12–month petition finding
Tucson shovel-nosed snake1
12–month petition finding
Northern leopard frog
12–month petition finding
Tehachapi slender salamander
12–month petition finding
Coqui Llanero
12–month petition finding
Susan’s purse-making caddisfly
12–month petition finding
White-sided jackrabbit
12–month petition finding
Jemez Mountains salamander
12–month petition finding
29 of 206 species
12–month petition finding
Desert tortoise – Sonoran population
12–month petition finding
Gopher tortoise – eastern population
12–month petition finding
Wrights marsh thistle
12–month petition finding
Southeastern pop snowy plover & wintering pop. of piping plover
90–day petition finding
Berry Cave
salamander1
90–day petition finding
Ozark chinquapin1
90–day petition finding
Smooth-billed ani
90–day petition finding
Bay Springs
salamander1
90–day petition finding
90–day petition finding
32 species of snails and slugs
90–day petition finding
Calopogon oklahomensis
90–day petition finding
Striped newt
90–day petition finding
American dipper – Black Hills population
90–day petition finding
Sprague’s pipit
90–day petition finding
Southern hickorynut
90–day petition finding
5 Southwest mussel species
90–day petition finding
Chihuahua scarfpea
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Mojave ground squirrel1
90–day petition finding
White-bark pine
90–day petition finding
Puerto Rico harlequin
90–day petition finding
Fisher – Northern Rocky Mtns. population
90–day petition finding
42 snail species (Nevada & Utah)
90–day petition finding
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ACTIONS FUNDED IN FY 2009 BUT NOT COMPLETED IN FY 2009—Continued
SPECIES
ACTION
HI yellow-faced bees
90–day petition finding
475 Southwestern species (partially completed)
90–day petition finding
HIGH PRIORITY LISTING ACTIONS 3
19 Oahu candidate species (16 plants, 3 damselflies) (15 with LPN = 2, 3 with LPN = 3, 1 with LPN = 9)
Proposed listing
17 Maui-Nui candidate species (14 plants, 3 tree snails) (12 with LPN = 2, 2 with LPN = 3, 3 with LPN = 8)
Proposed listing
Sand dune lizard (LPN = 2)
Proposed listing
2 Arizona springsnails (Pyrgulopsis bernadina (LPN = 2), Pyrgulopsis trivialis (LPN = 2))
Proposed listing
2 New Mexico springsnails (Pyrgulopsis chupaderae (LPN = 2), Pyrgulopsis thermalis (LPN = 11))
Proposed listing
2 mussels (rayed bean (LPN = 2), snuffbox No LPN)
Proposed listing
2 mussels (sheepnose (LPN = 2), spectaclecase (LPN = 4),)
Proposed listing
Ozark
hellbender2
(LPN = 3)
Proposed listing
Altamaha spinymussel (LPN = 2)
Proposed listing
5 southeast fish (rush darter (LPN = 2), chucky madtom (LPN = 2), yellowcheek darter (LPN = 2), Cumberland
darter (LPN = 5), laurel dace (LPN = 5))
Proposed listing
8 southeast mussels (southern kidneyshell (LPN = 2), round ebonyshell (LPN = 2), Alabama pearlshell (LPN =
2), southern sandshell (LPN = 5), fuzzy pigtoe (LPN = 5), Choctaw bean (LPN = 5), narrow pigtoe (LPN = 5),
and tapered pigtoe (LPN = 11))
Proposed listing
3 Colorado plants (Pagosa skyrocket (Ipomopsis polyantha) (LPN = 2), Parachute beardtongue (Penstemon
debilis) (LPN = 2), Debeque phacelia (Phacelia submutica) (LPN = 8))
Proposed listing
1
Funds for listing actions for these species were provided in previous FYs.
We funded a proposed rule for this subspecies with an LPN of 3 ahead of other species with LPN of 2, because the threats to the species
were so imminent and of a high magnitude that we considered emergency listing if we were unable to fund work on a proposed listing rule in FY
2008.
3 Funds for these high-priority listing actions were provided in FY 2008 and 2009
3 Funds for these high-priority listing actions were provided in FY 2008 and 2009
jlentini on DSKJ8SOYB1PROD with PROPOSALS3
2
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 we are considering new
information and will update our finding
at a later date (see 73 FR 23170, April
29, 2008). We also did not include new
information in our resubmitted petition
findings for the 48 candidate species for
which we are preparing proposed listing
determinations; see summaries below
regarding publication of these
determinations. We also funded revised
12–month petition findings for four
candidate species that we are removing
from candidate status, which are being
published as part of this CNOR (see
Candidate Removals). 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
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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 between the Listing
Program and the Candidate
Conservation Program.
During FY 2009, 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
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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
proposed or candidates for listing.
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Findings for Petitioned Candidate
Species
Below are updated summaries for
petitioned candidate 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’’).
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Mammals
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. This
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
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
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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
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
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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
long term 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. We estimate
that less than one third of the occupied
sites occur on conservation lands 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.
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
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uses in the region indicate that the rate
of change, about two 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
result in mortality or significantly
reduce the reproductive capacity 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 range in
California. Native populations of fisher
currently occur in the North Coast
Ranges of California, the KlamathSiskiyou Mountains of northern
California and southern Oregon, and in
isolated populations occurring in the
southern Sierra Nevada in California.
Descendents of a fisher reintroduction
effort also occur in the southern Cascade
Range in Oregon. In January of 2008, the
Washington Department of Fish and
Wildlife began to implement their fisher
recovery goals for the state through a
reintroduction effort in the Olympic
National Park. Estimates of fisher
numbers in native populations of the
West Coast DPS vary widely. A rigorous
monitoring program is lacking for the
northern California/southern Oregon
population making estimates of fisher
numbers for this relatively large
population difficult. The monitoring
program of the southern Sierra Nevada
population has provided preliminary
estimates. No estimates are available for
the introduced population in the
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southern Cascade Range in Oregon.
There is also a high degree of genetic
relatedness within some populations,
and populations of native fisher in
California are separated by four times
the species’ maximum dispersal
distance. The above-listed factors all
indicate that the likely extant fisher
populations are small and isolated from
one another.
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: uncharacteristically
severe wildfire, changes in forest
composition and structure related to the
effects of climate change, urban and
rural development, recreation
development, and highways. Major
threats to fisher that lead to direct
mortality and injury to fisher include:
Collisions with vehicles; predation; and
viral borne diseases such as rabies,
parvovirus, canine distemper, and
Anaplasma phagocytophilum. Existing
regulatory mechanisms on Federal,
State, and private lands affect key
elements of fisher habitat but do not
provide sufficient certainty that
conservation efforts will be effective or
will be 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, and since they significantly
affect this species’ reproductive
capacity. 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
which will affect the species over the
long-term. 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 population.
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
uses moist, streamside, dense riparian/
wetland vegetation. Recent genetic
studies confirm that the jumping mouse
is a distinct subspecies from other Z.
hudsonius subspecies, confirming the
currently accepted subspecies
designation.
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The threats that have been identified
are excessive grazing pressure, water
use and management, highway
reconstruction, development, recreation,
and beaver removal. Surveys conducted
in 2005 and 2006 documented a drastic
decline in the number of occupied
localities and suitable habitat across the
range of the species in New Mexico and
Arizona. Of the original 103 known
historical localities, 95 have been
surveyed since the early to mid-1990s.
Of the historical localities surveyed,
currently only 16 are extant, 9 in New
Mexico (including 1 that is contiguous
with the Colorado locality) and 7 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, and the populations in these
localities are small, 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, an ecosystem of
conservation concern (T. m. melanops is
found on alpine meadows in Olympic
National Park, and T. m. douglasii is
found in prairies 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.
Now, residential and commercial
development and ingrowth of woody
and/or nonnative vegetation have
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
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distributions in habitats highly desirable
for development and subject to a wide
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 Thomomys
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 habitat is
threatened by encroaching
development. Two gravel pits are
operating on part of the remaining Roy
Prairie pocket gopher habitat. 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, it is threatened or
endangered only in the significant
portion of the range in the montane
portions of central and south central
Colorado and north central New
Mexico, and we anticipate that if and
when it is listed, only that significant
portion of its range will be specified as
threatened or endangered. Within this
portion of the range, plague has
significantly reduced the number and
size of populations. Populations within
montane habitat have distinct
disadvantages in resisting the effects of
plague due to a higher abundance of
fleas that spread plague, smaller
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,
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roads, and oil and gas development each
currently affect a small percentage of
Gunnison’s prairie dog habitat. Plague is
significantly affecting the remaining
small, isolated populations, and 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.
Palm Springs round-tailed ground
squirrel (Spermophilus 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 is one of four
recognized subspecies of round-tailed
ground squirrels. This squirrel was
believed to be limited in range to the
Coachella Valley region of Riverside
County, California; however, results of
both a morphological study and a
genetic study indicate that its range may
be substantially larger. Upon receipt of
a finalized report detailing the methods
and results of the genetic study, the
Service will make a determination as to
whether listing of S. t. chlorus is still
warranted. Primary habitat for the Palm
Springs round-tailed ground squirrel is
the dunes and 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. Rapid growth of desert
cities such as Palm Springs and Palm
Desert in the Coachella Valley has
raised concerns about the conservation
of the Palm Springs round-tailed ground
squirrel. Urban development and drops
in the groundwater table have
eliminated approximately 90 percent of
the honey mesquite in the Coachella
Valley. Furthermore, urban
development has fragmented habitat
occupied by this squirrel thereby
isolating populations. The high rate of
urban development and associated
lowering of the groundwater table that
was likely historically responsible for
the high losses of honey mesquite sand
dune/hummocks habitat continues
today. We continue to assign the Palm
Springs ground squirrel subspecies an
LPN of 3 because the threats are ongoing
and are of a high magnitude as they
affect a large portion of its range and
significantly affect this subspecies’
survival.
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.
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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 approximately 38,756
hectares (95,767 acres), or 9 percent of
the known range. 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
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
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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 the
privately owned Threemile Canyon
Farms 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 wind
power development, among other forms
of development, continue to eliminate
Washington ground squirrel habitat in
portions of the species’ range.
Throughout much of their range,
Washington ground squirrels are
threatened by the establishment and
spread of invasive plant species,
particularly cheatgrass, which alter
available cover, food quantity and
quality, and increases 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 rangewide 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
large-scale efforts to convert suitable
habitat to agriculture, and wind power
project impacts can be minimized
through compliance with the Oregon
State Endangered Species Act (OESA) or
the Columbia Basin Ecoregion wind
energy siting and permitting guidelines.
The potential development of shooting
ranges on the Naval Weapons Systems
Training Facility is nonimminent
because the proposed action is still
being developed, making us unable to
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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
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
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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
(Coccyzus americanus) is a mediumsized 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
yellow-billed cuckoos that occur in the
western United States as a distinct
population segment (DPS). The area for
this DPS is generally west of the crest
of the Rocky Mountains.
The threats to the yellow-billed
cuckoo include habitat loss,
overgrazing, and pesticide 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 salt-cedar (Tamarisk
sp.). Overuse by livestock has been a
major factor in the degradation and
modification of riparian habitats in the
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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 is in the process of completing
a range wide conservation assessment
and strategy for the Western yellowbilled cuckoo. The assessment is in
early stages of development with work
beginning on a conservation strategy
sometime in 2010. We retained an LPN
of 3 for this population of yellow-billed
cuckoo; the threats are ongoing and
therefore imminent, and they are of a
high magnitude, because ongoing
habitat degradation significantly affects
the survival and reproductive capacity
of the DPS rangewide.
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
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
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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, 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 an area on Olosega
Island where 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
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 from British
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 agricultural fields,
seasonal wetlands, moderately to
heavily grazed pastures, seasonal
mudflats, airports, and dredge
deposition 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
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population is estimated to more than
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, and invasion of nonnative
plant species (e.g., Scot’s broom, sodforming grasses, and beachgrasses).
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 areas 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 overwintering
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 such as mowing,
recreational and military activities,
plowing, flooding, and dredge material
deposition during the nesting season, as
well as intentional disturbances such as
at the McChord Air Forece Base (AFB)
where falcons and dogs are used to haze
birds in order to avoid aircraft
collisions. In some areas, however,
landowners have taken steps to improve
habitat for streaked horned lark nesting.
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
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. Overwintering 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
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impact streaked horned lark breeding
and wintering (although current work
being conducted by The Nature
Conservancy may 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.
Threats are imminent, as a result of
continued loss of suitable lark habitat,
high nest-predation rates, and low adult
survival. Loss of habitat is a result of
plans for development on and adjacent
to several of its nesting areas, including
planned and/or 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 the use of
falcons and dogs to haze breeding birds
at McChord AFB, the annual Air Force
military training Rodeo event on
McChord AFB which included
firebombing on top of lark nesting
habitat, and the Air Expo on McChord
AFB. These two events usually occur in
alternate years. 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,
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.
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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 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.
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. Recently, peak counts at the
Delaware Bay area have been lower than
in the past and do not show a rebound.
The peaks were 13,315 in 2004; 15,345
in 2005; 13,455 in 2006; 12,375 in 2007;
and 15,395 in 2008. Counts in recent
years at the principal wintering areas in
South America also are substantially
lower than in the past.
The primary factor threatening the red
knot is 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. Since 1999,
a series of timing restrictions and
substantially lower harvest quotas have
been adopted by the Atlantic States
Marine Fisheries Commission (ASMFC),
as well as by the States of New Jersey
and Delaware. In May 2006, the ASMFC
adopted restrictions effective from
October 1, 2006, through September 30,
2008, including a prohibition on harvest
and landing of horseshoe crabs in New
Jersey and Delaware from January 1
through June 7; harvest of males only
from June 8 through December 31; and
harvest limited to no more than 100,000
horseshoe crabs per State per year. The
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ASMFC also adopted other restrictions
applicable to Maryland and Virginia. In
September 2008, the ASMFC Horseshoe
Crab Management Board approved an
addendum extending harvest
restrictions through October 31, 2009.
New Jersey established regulations in
2006 which superseded ASMFC
restrictions; resulting in a moratorium
on all horseshoe crab harvest in New
Jersey from May 15, 2006, through June
7, 2008. In March 2008, New Jersey
passed legislation imposing an openended moratorium on horseshoe crab
harvest or landing within the State until
such time as the red knot has fully
recovered. In February 2007, Delaware
imposed a 2–year moratorium, effective
January 1, 2007, on harvest of horseshoe
crabs within Delaware lands or waters.
In June 2007, following litigation by two
businesses involved in the harvesting
and sale of horseshoe crabs, Delaware’s
moratorium was overturned.
Consequently Delaware developed
regulations allowing for a male-only
horseshoe crab harvest, consistent with
restrictions adopted by ASMFC. In April
2009, the Maryland Department of
Natural Resources implemented a 2:1
male to female horseshoe crab harvest
ratio within Maryland waters.
The reductions in commercial harvest
since 1999 are substantial: In 1999 in
Delaware and New Jersey, 726,660
horseshoe crab landings for bait were
reported, compared to 173,177 in 2004
and a preliminary 2007 report of 76,663
crabs landed for bait in Delaware and no
horseshoe crabs landed in New Jersey as
a result of the State-imposed harvest
moratorium. However, scientists do not
know whether horseshoe crab
populations will rebuild or how long a
lag time there may be in increased
availability of eggs, as the species needs
8-10 years to reach sexual maturity, and
other key information for estimating
population response is lacking. Surveys
in Delaware Bay of horseshoe crab
spawning activity following
implementation of additional harvest
restrictions show that female horseshoe
crab spawning activity in Delaware Bay
has been stable for the overall period of
1999 through 2007 and male horseshoe
crab spawning increased during that
period. Spawning was likely suppressed
in 2008 by low water temperatures
resulting from a coastal storm.
Preliminary information for 2009
indicates that a high proportion of red
knots at the Delaware Bay stopover
attained threshold weight gains and
birds left the Delaware Bay stopover in
good condition. This weight gain
indicates that red knots found sufficient
horseshoe crab eggs or alternate forage
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resources during the 2009 stopover.
However, it remains to be seen if this
will be a long-term trend.
The numbers of red knots at key
wintering areas in South America
remained relatively steady from 2005
through 2007, inspiring some optimism
that the declining trend may have
ceased or slowed. In 2008, counts of red
knots within principal wintering areas
showed an all-time low of only 14,800
red knots, but then increased to 17,780
in 2009, similar to numbers found
during 2005-2007. Presence of an
increased number of juveniles and an
overall increase in red knots in
principal wintering areas likely
indicates a good breeding season in the
Arctic in summer 2008. However, the
long-term trend of counts of red knots
within the principal wintering areas in
Chile and Argentina shows a decline of
nearly 75 percent from 1985 to 2009.
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 species.
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 with solitary pairs
breeding 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
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concentrated and are subject to
subsistence harvest that at current levels
appears to be unsustainable, based on
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 harvet 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. 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 most of the
world’s population, inhabits Alaskan
coastal waters discontinuously from
Point Lay south to northern portions of
Southeast Alaska. Kittlitz’s murrelets
are associated with tidewater glaciers.
The current population estimate for
Kittlitz’s murrelets in Alaska is
approximately 19,578 birds. Kittlitz’s
murrelets in Alaska have declined at a
rate of up to 18 percent per year from
1989 to 2000 and new survey
information supports and strengthens
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the negative population trend estimates
that have been previously reported.
Threats to Kittlitz’s murrelets include
large-scale processes such as global
climate change and marine climate
regime shift. These large-scale processes
may influence Kittlitz’s murrelet
survival and reproduction. Glacial
retreat, a global phenomenon that affects
many of the glaciers where Kittlitz’s
murrelets are found, is associated with
changing forage fish availability and
may result in increased predation. Other
ongoing threats include oil spills,
bycatch in commercial gillnet fisheries,
and disturbance by tour boats. Kittlitz’s
murrelets are believed to have been
seriously affected by the Exxon Valdez
oil spill in Prince William Sound in
1989. Catastrophic events such as oil
spills could have a significant negative
effect on the population of this already
diminished species. Susceptibility to
mortality as bycatch in commercial
fishing could be a significant factor in
their population decline; Kittlitz’s
murrelets are caught in gillnets in
numbers disproportionate to their
density. 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 Alcid family that
occurs along the west coast of North
America in the United States and
Mexico. The species has a limited
breeding distribution, nesting only 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
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
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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, there are also plans to
remove rats from San Miguel Island, and
to restore nesting habitat on Santa
Barbara Island through the Montrose
Settlements Restoration Project, which
may benefit the Xantus’s murrelet
population at those islands.
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 lighting 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 and barn
owls 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.
While squid fishing has not occurred at
a particularly noticeable level near any
of the colonies in the Channel Islands
since 1999, this remains a potential
future threat.
A proposal to build three liquid
natural gas facilities near the Channel
Islands could cause impacts to the
nesting colonies. Although, none of
these facilities would be directly
adjacent to nesting colonies where their
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impacts would be expected to be more
significant, these facilities would
include bright lights at night and lights
from visiting tanker vessels, noise from
the facilities and from helicopters
visiting the facilities, and potential oil
spills associated with visiting tanker
vessels. However, these facilities are
early in complex and long-term
planning processes, and it is possible
that none of these facilities will be built.
In summary, the remaining threats to
the species are of high magnitude since
they have the potential to result in
mortality for a large portion of the
species’ range. However, the threats are
nonimminent since they are not
currently occurring at most of the
murrelet nesting sites. 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 cultivation,
conversion of suitable restored habitat
in the Conservation Reserve Program to
cropland, cumulative habitat
degradation caused by severe grazing,
and energy development, including
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 prairiechicken 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.
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Consequently, we have assigned an LPN
of 2 to this species.
Greater sage-grouse (Centrocercus
urophasianus), Columbia Basin DPS –
For the reasons discussed below, we
have not included new information in
our finding with regard to the Columbia
Basin DPS of the greater sage-grouse in
this notice. On May 14, 1999, we
received a petition 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 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 sagegrouse 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).
Legal actions are still pending for these
latter findings, which have been
remanded to the Service for further
consideration. In response, we initiated
a new rangewide status review for the
entire species (73 FR 10218). We will
update our candidate assessment and
publish a new finding for the Columbia
Basin DPS in the Federal Register
following completion of the new range
wide status review for the greater sagegrouse.
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
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
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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 constitues 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
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
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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
significantly affect the survival of this
DPS. Therefore, we assign this distinct
population segment an LPN of 3.
Elfin-woods warbler (Dendroica
angelae) – See above in ‘‘Listing Priority
Changes in Candidates.’’ The above
summary is based on information
contained in our files. No new
information was provided in the
petition we received on May 11, 2004.
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.
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. 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
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listing this species is warranted-butprecluded 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.
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,
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 or threatened 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 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 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, and 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
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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
remaining populations, particularly
those inhabiting private lands. We
retained an LPN of 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
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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
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 the private property, the
majority of the neighboring occupied
habitat is threatened by land
management activities (habitat
conversion to short-rotation 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
affected by these threats. Because all
extant populations are currently isolated
and fragmented by habitat loss in the
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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
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. Based on
nonimminent, high-magnitude threats,
we assigned a LPN 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. Due to
continuing drought, irrigated
agriculture, and development in the
region, surface water in the Rio Sonoyta
can be expected 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
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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, and northeastern and central
Nevada but local populations within
this general area appear to be small and
isolated from each other. Recent work
by researchers in Idaho and Nevada has
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, have and continue to
contribute to the degradation and
fragmentation of habitat. Emerging
fungal diseases such as
chytridiomycosis and the spread of
parasites are 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/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. While some
threats to the species and its habitat
(habitat modification and fragmentation,
nonnative species, inadequate
regulatory mechanisms, and climate
change) occur rangewide but at various
intensities, other threats (disease and
mining) affect only local populations;
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overall, the magnitude of the threats is
moderate. Based on ongoing, and
therefore, imminent threats of moderate
magnitude, we assigned a LPN 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 (Rana
mucosa) 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 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, and
morphological, and acoustic studies,
scientists recently recognized two
distinct species of mountain yellowlegged 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 recent
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. It is the
population of R. muscosa found in the
southern portion of the Sierra Nevada
that is a candidate for listing. R. sierrae
is not a candidate.
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 nonnative
fishes and mountain yellow-legged frogs
rarely co-exist. Mountain yellow-legged
frogs and trout (native and nonnative)
do co-occur at some sites, but these cooccurrences 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 yellowlegged frog, the Sequoia and Kings
Canyon National Parks have been
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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
watershed, and a tributary of Cole
Creek; no data showing increase in
mountain yellow-legged frogs at these
sites were available.
In California, chytridiomycosis, more
commonly known as chytrid fungus
(Batrachochytrium dendrobatidis), has
been detected in many amphibian
species, including the mountain yellowlegged frog within the Sierra Nevada.
Recent research has shown that this
pathogenic fungus is widely distributed
throughout the Sierra Nevada, and that
infected mountain yellow-legged frogs
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, of 43 populations assayed in
Yosemite National Park, 39 were
positive for chytrid fungus.
The current distribution of the Sierra
Nevada mountain yellow-legged frog is
restricted primarily to publicly managed
lands at high elevations, including
streams, lakes, ponds, and meadow
wetlands located on national forests,
including wilderness and
nonwilderness 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 on-going, 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
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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 predict a
10-percent decline per year in the
number of remaining Rana mucosa
populations. Based on threats that are
imminent (because they are ongoing)
and high-magnitude (because they affect
the survival of the DPS rangewide), we
continue 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
retained an LPN of 2 for the Oregon
spotted frog.
Relict leopard frog (Rana 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
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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 within the Virgin
River drainage downstream from the
vicinity of Hurricane, Utah; along the
Muddy River in Nevada; and along the
Colorado River from its confluence with
the Virgin River downstream to Black
Canyon below Lake Mead in 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
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 that is 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.
Conservation is proceeding under the
agreement; however, additional time is
needed to determine whether or not the
agreement 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 moderate to low. 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.
Ozark hellbender (Cryptobranchus
alleganiensis bishopi) – 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.
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,
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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
from the Edwards Aquifer that
discharges 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 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
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 these
ordinances. 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,
these ordinances 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. The threats are imminent
because urbanization is ongoing and
continues to expand over the Barton
Springs Segment of the Edwards Aquifer
and water quality continues to degrade.
Although 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
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species continues to be threatened by
occasional 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 threat to the entire population,
and is therefore a high-magnitude
threat. Thus, we retain an 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
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 the species. The Texas
Commission on Environmental Quality
(TCEQ) 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 these
ordinances. New developments are still
obligated to comply with regulations
that were applicable at the time when
project applications were first filed. In
addition, it is significant that even if
they were followed with every new
development, these ordinances 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.
Therefore, we do not rely on the
protection measures in our assessment
of threats.
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
working to protect habitat and acquire
land within the contributing watershed
for the Georgetown salamander. 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 assigned an 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 Williamson Counties, 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.
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 on 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
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‘‘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 these
ordinances. 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,
these ordinances 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.
Water quality impacts currently
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 retain an 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 Salado
salamander had not been sighted there
since 1991. Robertson Springs is on
private land and access to the site has
not been granted. The last survey at
Robertson Springs was in the early
1990s.
Primary threats to this species are
habitat modification and degradation of
water quality due to expanding
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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 vulnerable to catastrophic hazardous
materials spills, groundwater
contamination from 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 retained an
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). The Yosemite toad is a
moderately sized toad 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. The
Yosemite toad is 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 the Yosemite toad 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
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elevational range of the Yosemite toad is
1,460 to 3,630 m (4,790 to 11,910 ft).
The threats to 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 destroying 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 the
Yosemite toad and collapse rodent
burrows used by Yosemite toads as
cover and hibernation sites. Timber
harvesting and associated road
development could severely alter the
terrestrial environment and result in the
reduction and occasional extirpation of
amphibian populations in the Sierra
Nevada. Some of these threats result in
gaps in habitat which may act as
dispersal barriers and contribute to the
fragmentation of Yosemite toad habitat
and populations. Trails (foot, horse,
bicycle, or off-highway 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 the Yosemite
toad. Mass die-offs 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. The Yosemite toad is likely
exposed to a variety of pesticides and
other chemicals throughout its 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
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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.
Extensive survey work was conducted
in the 1990s to look for additional
populations. Currently, the species is
known from 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 (acres) of its habitat. These
impoundments are likely marginal or
unsuitable habitat for the salamander.
While the water-quality threat is
pervasive and problematic, the overall
magnitude of the threat is moderate,
reflected by the fact that there has not
been a steep rate of decline in the
population of this species. 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
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information contained in our files and
the 12–month finding published in the
Federal Register on May 3, 2006 (71 FR
26007). The headwater chub is a
moderate-sized cyprinid fish. The range
of the headwater chub has been reduced
by approximately 60 percent. Sixteen
streams (125 miles (200 kilometers) of
stream) are thought to be occupied out
of 19 streams (312 miles (500
kilometers) of stream) formerly
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
introductions of nonnative fish that prey
on them and compete with them for
food. These nonnative fish are difficult
to eliminate and, therefore, pose an
ongoing threat. 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 regions,
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
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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 believe 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, new information indicates
long-term persistence and stability of
existing populations. Currently 10 of the
16 extant 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 retained an LPN of
8 for this species.
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.
The Arkansas darter is a small fish in
the perch family native to portions of
the Arkansas River basin. The species’
range includes sites in extreme
northwestern Arkansas, southwestern
Missouri, and northeastern Oklahoma,
within the Neosho River watershed. It
also occurs in a number of watersheds
and isolated streams in eastern
Colorado, south-central and
southwestern Kansas, and the Cimarron
watershed in northwest Oklahoma. The
species is most often found in small
spring-fed streams with sand substrate
and aquatic vegetation. It appears stable
at most sites where spring flows persist.
It has declined in areas where spring
flows have decreased or been
eliminated. We estimate that currently
there are approximately 148 locality
occurrences of the Arkansas darter
distributed across the 5 States and that
a minimum of 12 populations or
population groups (metapopulations)
now exist. Threats to the species
include stream dewatering resulting
from groundwater pumping in the
western portion of the species’ range,
and potential development pressures in
portions of its eastern range. Spills and
runoff from confined animal feeding
operations also potentially affect the
species rangewide. The magnitude of
threats facing 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
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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.
Cumberland darter (Etheostoma
susanae) – We continue to find that
listing this species is warranted-butprecluded 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.
Pearl darter (Percina aurora) – See
above in ‘‘Listing Priority Changes in
Candidates.’’ The above summary is
based on information contained in our
files.
Rush darter (Etheostoma
phytophilum) – We continue to find that
listing this species is warranted-butprecluded 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.
Yellowcheek darter (Etheostoma
moorei) – We continue to find that
listing this species is warranted-butprecluded 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.
Chucky madtom (Noturus crypticus) –
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.
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
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
5 caves (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
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environment. The species’ karst habitat
is located down-gradient 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, chloride, and
potassium have been detected at levels
high enough to be detrimental to aquatic
life within the Perryville Karst area.
More than half 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 5 cave systems documented to
have grotto sculpins, populations in one
cave system were likely eliminated,
presumably as the result of point-source
pollution. When the cave was searched
in the spring of 2000, a mass mortality
of grotto sculpin was noted, and
subsequent visits to the cave have failed
to document a single live grotto sculpin.
Thus, the species appears to have
suffered a 20 percent decrease in the
number of populations from the single
event. 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. Thus, the magnitude of
threats is high. The threats are ongoing
and, therefore, are imminent. Thus, 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 within
the watershed. It has 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 within the
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upstream of Possum Kingdom Reservoir
is apparently stable, while the
population downstream of the reservoir
may only exist in remnant populations
in areas of suitable habitat, or may be
completely 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 high
since the major threat of reservoir
development within the species’ current
range may render its remaining habitat
unsuitable. The threats are
nonimminent because the most
significant threat - 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 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. Additional threats
include irrigation and water diversion,
sedimentation, desalination, industrial
and municipal discharges, agricultural
activities, in-stream sand and gravel
mining and the spread of invasive
saltcedar. The current limited
distribution of the smalleye shiner
within the Upper Brazos River Basin
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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 90 percent. The Zuni
bluehead sucker currently occupies 9
river miles (15 kilometers) in 3
headwater stream of the Rio Nutria in
New Mexico, and potentially occurs in
27 miles in (43 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
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
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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
believe 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 its historical habitat and the
populations are fragmented and isolated
from one another. The majority of
populations occur in high elevation
streams.
Major threats include: 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 additiona, 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
coldwater 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 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
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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 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 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 underway 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. In addition,
previously unknown locations where
the species persists were found in Texas
in 2008. Due to these ongoing
conservation efforts and the discovery of
new locations, the magnitude of the
threats is moderate. However, the
threats to the species are ongoing, and
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remain imminent. Thus, we maintained
a 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 endemic to the
Cumberland and Tennessee River
systems 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 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). Newly reintroduced
populations in the Little Tennessee,
Nolichucky, and Duck Rivers may 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
enrichment, and coal processing
pollution) that result in mortality or
reduced reproductive output. Since the
threats are ongoing, they are imminent.
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We assigned an LPN of 2 to this mussel
species.
Neosho mucket (Lampsilis
rafinesqueana) – See above in ‘‘Listing
Priority Changes in Candidates.’’ The
above summary is based on information
contained in our files. No new
information was provided in the
petition we received on May 11, 2004.
Alabama pearlshell (Margaritifera
marrianae) – We continue to find that
listing this species is warranted-butprecluded 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.
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
endemic to the Cumberland and
Tennessee River systems 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
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severely affected by numerous threats
(impoundments, sedimentation, small
population size, isolation of
populations, gravel mining, municipal
pollutants, agricultural runoff, nutrient
enrichment, and coal processing
pollution) that 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.
Altamaha spinymussel (Elliptio
spinosa) – We continue to find that
listing this species is warranted-butprecluded 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.
Snails
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
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
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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 and have a
significant effect on the survival of the
snails, 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
spring, its outflow channels, and the
land surrounding them are owned and
managed by The Nature Conservancy.
These snails are primarily threatened
with habitat loss due to springflow
declines from drought, pumping of
groundwater, and potentially 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 recently
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 maintain 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.
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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
snails. Because all of the threats occur
rangewide and have a significant effect
on the survival of this snail species,
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
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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 and have a significant
effect on the survival of this snail
species, 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
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
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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-butprecluded 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
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.
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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.
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.
Newcomb’s tree snail (Newcombia
cumingi) – We continue to find that
listing this species is warranted-butprecluded 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
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next annual resubmitted petition 12–
month 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
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-butprecluded 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 a stretch of thermal (between
45o and 32o Celsius, 113o and 90o
Fahrenheit) aquatic habitat that is
approximately 600 m (1,968 ft) long and
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2 m (6.7 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.
Conservation measures implemented
recently 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 this species 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 located three
additional populations bringing the total
known to 16.
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 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
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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
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 (Forest Service, Fort
Huachuca, The Nature Conservancy) are
including consideration for the
springsnail or other co-occurring listed
species in their activities (e.g., 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) – We continue to find that
listing this species is warranted-butprecluded 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.
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Page springsnail (Pyrgulopsis
morrisoni) – 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 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. Arizona
Game and Fish Department 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. A draft Candidate
Conservation Agreement with
Assurances was published and available
for public review and comment on
January 28, 2008. This Agreement
should be finalized during 2009, at
which time we will reassess the LPN to
ensure the magnitude and immediacy of
threats are still appropriately described.
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. The magnitude of threats is
high because limited distribution of this
narrow endemic makes any detrimental
effects from threats likely to result in
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 retained an LPN of 2 for
the Page springsnail.
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-butprecluded 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.
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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
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
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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 on by alien ants and
parasitized by native and nonnative
parasitoids. 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.
These threats are imminent because
they are ongoing. Therefore, we
assigned an LPN of 2 for this species.
Miami blue butterfly (Cyclargus
thomasi bethunebakeri) – See above in
‘‘Priority Changes in Candidates.’’ The
above summary is based on information
contained in our files and in the petition
we received on June 15, 2000.
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 5000
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
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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
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
to1996 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
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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 mortality 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
adversely 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
negative 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
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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
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
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
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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 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
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 2008 flight period, butterflies
were detected in just 8 populations. The
total number of Taylor’s checkerspot
butterflies was considerably reduced in
current surveys with approximately
2,300 individuals observed rangewide.
The latest decline observed was from
the Fort Lewis population where fewer
than 200 butterflies were counted.
Currently, just five populations had
butterflies in flight in Washington, two
in the Willamette Valley of Oregon, and
one on Denman Island, British
Columbia, Canada. A new population
was observed on the Olympic National
Forest.
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 the past
year and the site where Taylor’s
checkerspot were known to thrive on
Fort Lewis was severely affected by
Armored Vehicle training. The outcome
of the training’s effect will not be
determined until after this year’s
monitoring has been completed.
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.
The grassland ecosystem on which
this subspecies depends requires annual
management to maintain suitable
grassland habitat for the species.
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 prairies when
processes like fire, or its surrogate
mowing, do not take place. Threats also
include the loss of prairies to
development or the conversion of native
grasslands to agriculture. Vehicle and
foot traffic that crushes larvae and larval
host plants on roads where host plants
have become established are also
threats; these areas act as a mortality
sink at several of the north Olympic
Peninsula sites.
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 affect the survival of the subspecies.
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 continue to assign
the Taylor’s checkerspot butterfly a
listing priority number of 3.
Blackline Hawaiian damselfly
(Megalagrion nigrohamatum
nigrolineatum) – We continue to find
that listing this species is warrantedbut-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.
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 petition 12–month 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
petition 12–month finding.
Orangeblack Hawaiian damselfly
(Megalagrion xanthomelas) – The
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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 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
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stage from nonnative tipulid flies,
which feed within the same portion of
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;
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inbreeding, population isolation, and
prescribed fire threatens some
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 a 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
2009. 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.
Threats to the Mardon skipper include
direct impacts to individuals and local
populations by off-road vehicle use,
livestock grazing, and pesticide drift.
Habitat destruction or modification
through conifer encroachment, invasive
nonnative plants, roadside maintenance,
and grassland/meadow management
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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 assigned 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. The
Coral Pink Sand Dunes tiger beetle
occurs only at the Coral Pink Sand
Dunes, 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. In addition, the beetle’s
habitat is being adversely affected by
ongoing, recreational off-road vehicle
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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 Bureau of
Land Management, 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 have
retained an LPN of 2 for this species
primarily 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
found at 40 sites from near Haines City
south to Josephine Creek. 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 suggest that the actual
population size at the various survey
sites is likely to be as much as two times
as high as indicated by the visual index
counts.
Lack of fire to create open sand,
habitat loss and fragmentation, and
small and isolated populations pose
serious threats to this species. Overcollection and pesticide use are
additional concerns. Because this
species is narrowly distributed with
specific habitat requirements and small
populations, any of the threats could
have a significant impact on the survival
of the species. 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.
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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 a 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
occurs on the islands of Maui and
Hawaii are located within State Natural
Area Reserves (NAR). Hawaii’s State
statutes prohibit the collection of the
species and the disturbance of the pools
in State NARs. However, enforcement of
collection and disturbance prohibitions
is difficult, and the negative effects from
the introduction of fish are extensive
and happen quickly. In addition, the
pools where this species occurs on the
island of Oahu do not receive protection
from collection of the species or
disturbance of the pools. Therefore,
threats to this species could have a
significant adverse effect on the survival
of the species, and are of a high
magnitude. However, the primary
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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
three populations on the island of Maui
and one population 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 National Park, and
collection and disturbance are also
prohibited. However, enforcement of
these prohibitions is difficult, and the
negative effects from the introduction of
fish are extensive and happen quickly.
Therefore, threats to this species could
have a significant adverse effect on the
survival of the species, 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 populations on the
island of Maui and one population on
the island of Hawaii. The primary
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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. 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 conservation
efforts underway to alleviate the
potential for any of these threats in the
one pool on the island of Hawaii.
Therefore, threats to this species could
have a significant adverse effect on the
survival of the species, 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
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. All
individuals of this species may be
adversely affected by a single dumping
of trash or release of nonnative fish in
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its 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 a small
perennial herb, 2.5 to 15.2 centimeters
(1 to 6 inches) across forming compact
mats with lavender-pink, trumpetshaped, and generally fragment flowers.
Abronia alpina is known from one main
population center in Ramshaw Meadow
on the Kern Plateau of the Sierra
Nevada, California and from one
subpopulation found in adjacent
Templeton Meadow. 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 surveyed in 2007.
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 and at times
comes 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
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SFKR. Drying out of the meadow system
could potentially affect A. alpina
pollinators and 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
ten-year moratorium on the Templeton
allotment that 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. We continue to assign an
LPN of 11 for A. alpina based on
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,
approximately 20 populations are
known from the Gulf 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, rather 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 (20)
across multiple counties in two states
and due to the fact that several sites are
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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 disturbed areas at the edges
of natural areas. Plants can be found
growing from crevices on limestone, or
on sand. The pine rockland 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 27 extant
occurrences, 12 in Monroe County and
15 in Miami-Dade County; many
occurrences are on conservation lands.
However, 4–5 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
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 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 this threat where
possible. While some of the 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
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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 Miller Island 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
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 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
64,000 acres. Available information
from 2000 indicates that the species
remains stable. Previous and ongoing
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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
this year 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 and, 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 petition 12–month finding.
Bidens campylotheca ssp. pentamera
(Kookoolau) – We continue to find that
listing this species is warranted-butprecluded 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.
Bidens campylotheca ssp. waihoiensis
(Kookoolau) – We continue to find that
listing this species is warranted-butprecluded 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.
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
listing rule that we expect to publish
prior to making the next annual
resubmitted petition 12–month finding.
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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. This subspecies is an
erect, perennial herb found in open
mixed shrubland to dry Metrosideros
(ohia) forest on the island of Hawaii,
Hawaii. This subspecies is endemic to
the island of Hawaii, where wild
populations are restricted to an area of
less than 10 square miles (26 square
kilometers). Bidens micrantha ssp.
ctenophylla is known from four wild
and four outplanted populations
totaling approximately 130 to 140
individuals, the majority of which occur
in only two (wild) populations. This
subspecies is threatened by fire and
nonnative plants, and two populations
are threatened by residential and
commercial development. The threats to
B. micrantha ssp. ctenophylla from fire
and nonnative plants are of a high
magnitude and imminent because they
are occurring rangewide, they threaten
the continued existence of the species,
and no efforts for their control have
been undertaken. 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 population is known to exist;
15 other occurrences contain less than
100 individuals. Eleven occurrences are
on conservation lands. 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
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
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management of privately owned pine
rockland habitats in Miami-Dade
County and projects to restore suitable
habitat and reintroduce and establish
new populations of the plants in pine
rocklands. 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. This species is a robust, shortrhizomatous perennial found in wet
forest, open bogs, and bog margins on
the islands of Maui and Hawaii, Hawaii.
Historically rare, C. expansa was
restricted to wet forest and bogs on
Maui. Its historical status is unknown
on Hawaii. Currently, this species is
known from 11 populations totaling
approximately 230 individuals on Maui,
and was recently discovered in nine
populations totaling approximately 350
individuals on the island of Hawaii.
Calamagrostis expansa is threatened by
pigs that degrade and destroy habitat
and by nonnative plants that
outcompete and displace it. Feral pigs
have been fenced out of most of the west
Maui populations, 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 and at
all of the populations on the island of
Hawaii. Therefore, overall the threats
from feral pigs and nonnative plants are
of a high magnitude and imminent for
C. expansa, and we retained an LPN of
2 for this species.
Calamagrostis hillebrandii
(Hillebrand’s 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 hillebrandii is a slender,
short-rhizomatous perennial found in
Metrosideros-Machaerina (ohia-uki)
montane wet bog or MetrosiderosRhynchospora-Oreobolus (ohiakuolohia-oreobolus) mixed bog on Maui,
Hawaii. This species is known from two
populations of fewer than 2,000
individuals, restricted to the bogs of
west Maui. There is an unconfirmed
report of C. hillebrandii from central
Molokai. This species is currently
threatened by pigs that degrade and
destroy habitat and nonnative plants
that outcompete and displace it. A
portion of one population is protected
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by an ungulate exclosure fence while
the second population may indirectly
benefit from conservation actions for
ungulate control and control of
nonnative plants conducted in a nearby
preserve. The threats are imminent
because they are ongoing in one of the
two known populations. The threats are
high in magnitude because they result
in direct mortality or significantly
negatively affect the reproductive
capacity of this species. Therefore, we
retained an LPN of 2 for this species.
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 four
individual mountain peaks in the
Klamath National Forest and on private
lands. The northern-most 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 southern-most 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.
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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, and
competition from exotic plants threaten
the continued existence of this species.
These threats are of high magnitude
because of their potential to negatively
affect the overall survival of the species.
Because the 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.
Awikiwiki is a perennial climber found
in open lava fields and lowland dryland
forest on Maui and Lanai, and is
possibly on the island of Niihau,
Hawaii. This species is known from five
populations totaling a little over 200
individuals. This species 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. An ungulate
exclosure fence protects six individuals
of C. pubescens, and weed control is
ongoing at this location on Maui. This
species is represented in two 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
significantly affect the species
throughout its range. 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
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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.
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 2005,
2006, and 2007, it still persists and has
increased in some 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,
although they too are imminent. 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
protect this potentially large population
of plants. 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
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encroach on pine rockland and this
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 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 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
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. 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. 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 lands and on
one county-owned 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
difficulty of applying prescribed fire,
and exotic plants. These threats are
severe within small and unmanaged
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fragments in urban areas. However, the
threats of fire suppression and exotics
are reduced on lands managed by the
National Park Service. Another threat is
hydrology changes. 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 could
negatively affect the pinelands of Long
Pine Key. 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, since
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
the extent to which proposed restoration
will negatively affect this subspecies are
unclear. Overall, the threats are
nonimminent since fire management at
the largest occurrence is regularly
conducted, and sea-level rise and
hurricanes are longer-term threats.
Therefore, we assigned a 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
densities) and usually, exposed rock or
gravel.
Pine rockland communities are
maintained by relatively frequent fires.
In the absence of fire, shrubs and trees
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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 hurricanerelated storm surges, in combination
with a limited, fragmented distribution
and threats from sea-level rise, results in
a moderate magnitude of threat, in part,
because a large part of the range is on
conservation lands wherein some
threats can be substantially controlled.
The immediacy of hurricane threats is
difficult to categorize. 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. Chorizanthe parryi var. fernandina
grows up to 30 centimeters in height
and 5 to 40 centimeters across. The
plant currently is known from two
disjunct localities: the first is in the
southeastern portion of Ventura County
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
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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 San
Fernando Valley spineflower 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 several 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 is a recently identified threat to
the species, and the potential impacts to
Chorizanthe parryi var. fernandina have
not yet been fully evaluated. 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 evidenced by
the destruction of some plants during
installation of an agave farm.
Furthermore, cattle grazing on Newhall
Ranch may be a current threat. Cattle
grazing may harm Chorizanthe parryi
var. fernandina by trampling plants and
compacting soil. Grazing activity could
also alter the nutrient content of the
soils 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.
The threats to this plant are high in
magnitude since Chorizanthe parryi var.
fernandina is particularly vulnerable to
extinction due to its concentration in
two isolated 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,
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drought, or erosion. The primary threat
from habitat destruction by
development is nonimminent due to the
ongoing development of a CCA. We
retained a listing priority number of 6
for Chorizanthe parryi var. fernandina
due to a 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 at five
islands in the Florida Keys; two
occurrences are within Everglades
National Park (ENP). 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. More recently,
an estimate of 1,500 plants was given for
areas 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 appeared to have had
severe impacts, at least in the shortterm. Occurrences probably declined
due to inundation of its coastal barren
and rockland hammock habitats in the
short-term; long-term effects on this
species are unknown. Sea-level rise is
considered a major threat over the longterm. 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, especially
following Hurricane Wilma. Thus, these
factors constitute a high magnitude of
threat. The threats of small population
size, isolation, and uncertain viability
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,
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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 the population was
estimated by Biscayne National Park
staff to consist of at least 600 plants. The
cactus does not propagate sexually, and
asexual reproduction is the main lifehistory 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), Little Torch Key, and
Big Pine Key (outplanting; lower Keys)
populations are clonally derived and
genetically distinct from each other.
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
crown rot disease. Because of low
population numbers, lack of variation
between and within populations, and
reproductive problems, the threats are of
high magnitude. 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
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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.
Additionally, the species is reported as
common on Anegada Island.
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 may be
threatened by management and
maintenance activities; another 32
percent of the currently known
reproductive adults are located on
privately owned property where habitat
destruction or modification may affect
this species. Since threats may
significantly affect the majority of the
reproducing population, the magnitude
of the threats is high. The population of
C. rupicola on Anegada Island is
currently in good condition and the
threats this species faces there are ones
that will arise in the future, if
conservation measures are not
implemented and long-term impacts are
not averted. For these reasons, the
threats to the species as a whole are
nonimminent. Therefore we have
assigned a LPN of 5 to this species.
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 petition 12–month 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
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 petition 12–month finding.
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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 petition 12–month 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
petition 12–month finding.
Cyanea tritomantha (1Aku) – 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. This species is known from
16 populations with a total of
approximately 300 to 400 individuals.
Cyanea tritomantha is threatened by
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 that
may directly prey upon and defoliate
individuals, and human trampling of
individuals 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
other 13 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. They are ongoing
and therefore imminent for more than
seventy-five 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) – 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.
Haiwale is a shrub found in lowland to
montane wet forest on Maui and
Molokai, Hawaii. Historically rare, C.
filipes was found in southeastern
Molokai and west Maui. Currently, this
species is known from 10 populations,
3 on Molokai and 7 on west Maui,
totaling approximately 2,000
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individuals. There is some question as
to the true identity of the Maui
populations, which do not fit the
description of the species precisely. If,
upon further taxonomic study, the Maui
populations are determined not to be
this species, then it is even rarer, with
only the Molokai populations of a few
individuals remaining. Cyrtandra filipes
is threatened by pigs, goats, and deer
that degrade and destroy habitat and
may prey upon it, by nonnative plants
that outcompete and displace it, and
potentially by predation by rats and
slugs. Landslides are a likely threat to
two populations. Feral pigs have been
fenced out of one population of C.
filipes on Maui, and strategic fencing for
axis deer is under construction on west
Maui, but deer are able to jump over
most pig exclusion fences, so they are
still considered a threat. Nonnative
plants are being reduced in the
population that is fenced but all
populations are potentially threatened
by rats and slugs. The threats from pigs
and nonnative plants are of a high
magnitude because of their severity and
the fact that they occur in eight of the
10 known populations. In addition,
these threats are imminent because they
are ongoing. Therefore, we retained an
LPN of 2 for this species.
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 petition 12–month 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 petition 12–month 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 petition 12–month 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,
Florida. It is also known from small
populations in Miami-Dade County.
There are a total of nine extant
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occurrences, most of which are on
conservation land.
Existing occurrences are extremely
small and may not be viable, especially
those in Miami-Dade County.
Remaining habitats are fragmented.
Climatic changes and sea-level 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 off-road
vehicles is a serious threat within the
BCNP; the threat from 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 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,
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, and threats
are imminent because of the limited
number of occurrences and the small
number of individual plants at each
occurrence. In addition, 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. D. hirstii is a perennial grass that
produces erect leafy flowering stems
from May to October. D. 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
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known sites could result in a serious
protraction of the species’ range.
However, the most immediate and
severe of the threats to this species (i.e.,
ditching of the Laboundsky 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
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. Although
privately owned pine rocklands and
prairies are at risk to development, the
plants on Federal lands are protected
from this threat. However, extant
occurrences are in low-lying areas and
will be affected by climate change and
rising sea level.
This species is threatened by habitat
loss and degradation due to fire
suppression, the difficulty of applying
prescribed fire to pine rocklands, and
exotic plants. Since the only remaining
populations 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 have been threatened
by off-road vehicle use. Another threat
is hydrology changes. 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.
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Overall, the magnitude of threats is high
because only two occurrences remain,
and various threats exist. Impacts from
climate change and sea-level rise are
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 1300 to 2000
feet elevation.
Habitat 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. The
threats are imminent, mainly due to the
continued decline of the species, most
likely from effects from the on-going
drought. Conditions in 2006 to 2008
worsened, and the drought is prevalent
throughout the range of this variety. For
this reason, drought as the main threat
is on-going and is a significant threat to
the long-term viability 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
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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
the ground. Plants that are much higher
on the cliff face would probably not be
affected. We consider the magnitude of
threats to be moderate rather than high
because we believe 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 eight 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 2009,
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
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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 be
vulnerable to these threats, we retained
an LPN of 2 for this species.
Eriogonum corymbosum var. nilesii
(Las Vegas buckwheat) – The following
summary is based on information
contained in our files and the petition
we received on April 23, 2008. The Las
Vegas buckwheat 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. The Las Vegas buckwheat is very
conspicuous when flowering in late
September and early October. It is
restricted to gypsum soil outcroppings
in Clark and Lincoln Counties, Nevada.
Only recently has the taxonomy been
verified using molecular genetic
analyses.
Loss of habitat from development is a
significant threat with over 95 percent
of the historical range and potential
habitat of the subspecies lost to
development. In 2005, the Las Vegas
buckwheat was known from 9 locations
on approximately 1,150 acres. However,
since that time, approximately 290 acres
were or soon will be developed, and the
current distribution of the plant
occupies about 890 acres. In addition,
off-highway vehicle activity and other
public land uses (casual public use,
mining, and illegal dumping) directly
and indirectly threaten over half of the
remaining habitat. To date, regulatory
mechanisms to protect the Las Vegas
buckwheat are inadequate. Its
designation as a Bureau of Land
Management (BLM) special status
species and limited resource and law
enforcement personnel have not
provided adequate protection on lands
managed by the BLM. The Las Vegas
buckwheat is not protected by the State
of Nevada or any other regulatory
mechanisms on other federal lands.
Conservation measures are being
developed that could reduce the risks to
occupied habitat, but we believe it
would be premature to consider these
measures sufficiently complete as to
remove these threats. The magnitude of
threats is high since the more significant
threats (development and surface
mining) would result in direct mortality
of the plants in over half of its known
habitat. While both development and
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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 the Las Vegas buckwheat
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
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, in
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 impacted, and perhaps
eliminated by fire control efforts. The
primary threat of surface mining is high
in magnitude because it could extirpate
the species in the majority of its range.
That threat is nonimminent because
none of the mining claims are active.
Because of the high-magnitude,
nonimminent threat to the small,
scattered populations, we assigned a
listing priority number of 5 to this
species.
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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. Festuca hawaiiensis is known
from four populations totaling
approximately 1,000 individuals in and
around the Pohakuloa Training Area
(PTA). Historically, this species was
also found on Hualalai and Puu
Huluhulu on Hawaii and possibly
Ulupalakua on Maui, 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 areas but the majority of this
population is still affected by threats
from fire and will require long-term
monitoring and management. The
threats are imminent because they are
not controlled and are ongoing in the
remaining, unfenced populations.
Firebreaks have been established at two
other populations but again fire is an
imminent threat to the other two
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. 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.
Five 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 five years, in the
Chisos Mountains, Big Bend National
Park, Texas, and in the privately owned
Maderas del Carmen protected natural
area in Coahuila. Despite intensive
searches, a population known from
Guadalupe Mountains National Park,
Texas has not been found since 1952
and is presumed extirpated. 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
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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
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. We have assigned a LPN
of 11 to 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.
Nanu is a tree found in mesic to wet
forest on the islands of Kauai, Molokai,
Maui, and Hawaii, Hawaii. Gardenia
remyi is known from 20 populations
totaling between 77 and 104
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. It 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
signifcantly affect the entire species
resulting in direct mortality or reduced
reproductive capacity. 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
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prior to making the next annual
resubmitted petition 12–month finding.
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 petition 12–month 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
endemic to Puerto Rico. Currently, G.
concolor is known from two
populations: one at Cerro La Santa and
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 four individuals
located at Charco Azul.
The species is threatened by habitat
disturbance related to the maintenance
of existing telecommunication facilities
at Cerro La Santa, limited distribution
(two sites), low population numbers
(less then 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 always effectively enforced and
Service personnel have documented
some damage to the population located
adjacent to existing communication
towers at the forest. Because of
extremely low population numbers and
the vulnerability to threats
(maintenance activities and hurricanes),
the magnitude of current threats on the
species is high. Overall, threats are
nonimminent since G. concolor is
located in the Carite Commonwealth
Forest, administered and managed by
the DNER for conservation and
recreation, and actions that may affect
such species are generally scrutinized
and measures to minimize or avoid
impacts to these species are
recommended and implemented.
Therefore, we have assigned a listing
priority number of 5 to this species.
Hazardia orcuttii (Orcutt’s hazardia) –
The following summary is based on
information contained in our files and
the petition we received on March 8,
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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 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.
Hazardia orcuttii also occurs at a few
coastal sites in Mexico, where it has no
conservation protections. The
occurrences in Mexico are threatened by
coastal development from Tijuana to
Ensenada. There are approximately 668
native adult plants and 50 seedlings
remaining in the U.S., and the
population in Mexico is estimated to be
1300 plants. Because the extant
population in the U.S. is within an area
that receives a great deal of public use,
trampling, dumping, and other
unintentionally destructive impacts are
affecting these Hazardia orcuttii plants.
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. 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 although trampling and
other recreational impacts are ongoing,
the most significant threats (invasive
nonnative plants and low reproductive
output) are nonimminent and long-term
in nature. This species faces highmagnitude nonimminent threats so we
have 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.
Kamapuaa is a scandent shrub found in
mixed shrubland to wet lowland forest
on Oahu and Kauai, Hawaii. This
species is known from 12 populations
totaling 1,000 to 1,400 individuals.
Hedyotis fluviatilis is threatened by pigs
and goats that degrade and destroy
habitat, and by nonnative plants that
outcompete and displace it. Landslides
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are a potential threat to populations on
Kauai. This species is represented in ex
situ collections; 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) – See above in ‘‘Listing
Priority Changes in Candidates.’’ The
above summary is based on information
contained in our files. No new
information was provided in the
petition we received on May 11, 2004.
Hibiscus dasycalyx (Neches River
rose-mallow) – The following summary
is based on information contained in
our files. No new information was
provided in the petition received on
May 11, 2004. 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. A Candidate
Conservation Agreement was developed
for this site, but smaller plant numbers
have been seen in recent years, 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 and will be reassessed
in the near future. 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
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protect this land in perpetuity. In east
Houston County, a population
discovered in Compartment 55 in Davy
Crockett National Forest numbered over
1000 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
prevented further assessment of these
rose-mallow sites.
The threats to the species continue to
be of a high magnitude because they can
severely affect the survival and
reproductive capacity of the species.
Overall the threats are nonimminent
since they are not currently affecting or
likely to affect the majority of the
populations of this species in the
immediate future. Thus, we have
retained an LPN of 5 for the Neches
River rose-mallow.
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. 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 4.8 million
individuals at 14 known sites. The
Nevada sites support nearly 98 percent
of the total number of individuals (4.7
million) on about 30 acres (12 hectares)
of occupied habitat. The California sites
are larger in area, totaling about 156
acres (63 hectares), but support fewer
individuals (approximately 115,000).
The primary threats to I. webberi
include urban development, authorized
and unauthorized roads, off-road
vehicle activities and other dispersed
recreation, livestock grazing and
trampling, fire and fire suppression
activities including fuels reduction and
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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 committed to develop a
conservation strategy and monitoring
program to protect this species on
National Forest lands where most
population 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
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 Webber ivesia are
nonimminent and retained an LPN of 5
for this species.
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. Ohe is an erect herb found in wet
to mesic Metrosideros polymorphaAcacia koa (ohia-koa) forest on the
islands of Kauai, Oahu, Molokai, Maui,
and Hawaii, Hawaii. Ohe is known from
38 widely scattered populations totaling
approximately 180 individuals
throughout its range. Plants are typically
found as only one or two individuals,
with miles between populations. This
subspecies is threatened by destruction
or modification of habitat due to 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
a few populations that are fenced.
However, these threats are not
controlled and are ongoing in the many
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 mortaility or adversely affect the
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reproductive capacity of the majority of
populations of this species. 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 petition 12–month finding.
Leavenworthia crassa (Gladecress) –
The following information is based on
information contained in our files. No
new information was provided in the
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, Alabama, 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. 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.
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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 1000
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.
An introduced population in
Nacogdoches County numbered about
1000 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) – See above in
‘‘Listing Priority Changes in
Candidates.’’ The above summary is
based on information contained in our
files. No new information was provided
in the petition we received on May 11,
2004.
Linum arenicola (Sand 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.
Sand flax is found in pine rockland and
marl prairie habitats which require
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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 are
extirpated or destroyed. Only small and
isolated occurrences remain in lowlying areas in a restricted range of
southern Florida and the Florida Keys.
Habitat loss and degradation due to
development is a major threat; most of
the remaining occurrences are on
private land or non-conservation public
land. However, much of the pine
rockland on Big Pine Key, the location
of the largest occurrence, is protected
from development. Climatic changes
and sea-level rise are long-term threats
that are expected to affect the species
and ultimately reduce the extent of
available habitat. Nearly all remaining
populations are threatened by fire
suppression, difficulty in applying
prescribed fire, road maintenance
activities, exotic species, or illegal
dumping. However, some efforts are
underway to use prescribed fire to
control exotics on conservation lands
where this species occurs. Sand flax is
vulnerable to natural disturbances, such
as hurricanes, tropical storms, and
storm surges. Hurricane Wilma
inundated most of its 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. Due to the small and fragmented
nature of the current population,
stochastic events, disease, or genetic
bottlenecks may strongly affect this
species. 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.
Overall, the magnitude of threats is
high; most threats are ongoing and thus
are imminent. Therefore, we assigned an
LPN of 2 to this species.
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 9
known occurrences. Occurrences with
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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 9 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. The species 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
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 petition 12–month 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 petition 12–month 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 petition 12–month 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 cloud swept ridges
and lowland mesic and wet forest on
Kauai and Oahu, Hawaii. This species is
currently known from 11 populations
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totaling approximately 58 individuals
on Kauai and from 8 populations
totaling between 73 and 83 individuals
in the Koolau Mountains of Oahu.
Myrsine fosbergii is threatened by feral
pigs and goats that degrade and destroy
habitat and may prey upon the plant,
and 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 petition 12–month finding.
Narthecium americanum (Bog
asphodel) – 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. Bog asphodel is a perennial herb
that is found in savannah 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, but it is now only
found within the Pine Barrens region of
New Jersey.
As an obligate wetland species, N.
americanum is threatened by loss of
habitat due to filling or draining of
wetlands, changes in hydrology, and
indirect impacts from development in
adjacent uplands. The Pine Barrens
savannahs 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. Within its
savannah habitats, bog asphodel appears
limited to a relatively narrow range of
hydrologic and topographic conditions
that make this species particularly
sensitive to hydrologic changes, such as
those resulting from filling or draining
of wetlands, flooding as a result of
reservoir construction, water extractions
or diversions, and conversion of natural
wetlands to commercial cranberry bogs.
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Most bog asphodel occurs in New
Jersey’s regulated Pinelands Area, in
which development of wetlands or
uplands is prohibited unless designed to
avoid irreversible adverse impacts upon
the survival of any local populations of
federally or State-listed plant or animal
species. However, exemptions are
granted for cranberry production and
other agricultural uses, and illegal
wetland filling has occurred. Outside
the Pinelands Area, wetlands and
wetland buffers are State-regulated, but
many activities in uplands are not.
Cumulative effects of upland
development impact wetlands through
sedimentation, non-point source
pollution, changes in pH, and lowered
water tables.
Of the known extant populations of
bog asphodel, at least 55 occur on Stateowned lands, 4 occur on federally
owned lands, and at least 13 occur on
private lands. Bog asphodel occurrences
on public lands receive the highest
levels of protection, but lack of
enforcement regarding off-road vehicles
is a problem on both public and private
lands. Over-collection, as well as
trampling, erosion, and siltation caused
by recreational activities, may also affect
some populations. Natural threats to bog
asphodel at some sites include beaverinduced flooding, succession of
savannahs to Atlantic white cedar
swamps, and suppression of natural
wildfires. The threats are moderate in
magnitude since many occurrences
receive some level of protection from
some threats. The threats are imminent
because conversion to cranberry bogs,
natural succession, wildfire
suppression, recreational impacts, and
erosion are all ongoing. Overall, based
on these imminent, moderate threats,
we retain a listing priority number of 8
for this species.
Nothocestrum latifolium (1Aiea) – 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.
Aiea is a small tree found in dry to
mesic forest and diverse mesic forests
on Kauai, Oahu, Maui, Molokai, and
Lanai, Hawaii. Nothocestrum latifolium
is known from 20 steadily declining
populations totaling fewer than 1,100
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 some areas where N.
latifolium currently occurs, and
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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. 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.
Holei is a tree found often on lava and
in dry to mesic forest on the islands of
Hawaii and Maui, Hawaii. This species
is currently known from 11 populations
totaling fewer than 130 individuals.
Ochrosia haleakalae is threatened by
fire; feral pigs, goats, and cattle that
degrade and destroy habitat and may
directly prey upon it; and 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
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, and
adversely affects the survival and
reproductive capacity of the majority of
the species. 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.
The Fickeisen plains cactus 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 well-drained hills
in Navajoan desert or grassland. In 1999,
the Arizona Game and Fish Department
noted 23 occurrences for the species,
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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 humaninduced threats to this cactus are
activities associated with road
maintenance, off-road 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
since 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 debilis (Parachute
beardtongue) – We continue to find that
listing this species is warranted-butprecluded 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.
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. The White River beardtongue 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 can
expose 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. The
threats are of high magnitude because
they involve habitat destruction that
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could adversely affect the majority of
the occurrences of this plant variety.
The threats are nonimmient because
threats associated with oil and gas and
oil shale development will probably not
be increasing substantially within the
near future. Oil shale development
remains uncertain within the species’
habitat, and is not expected to be a
significant factor in the near term.
Therefore, based on current information,
we retained an LPN of 6.
Peperomia subpetiolata (1Ala 1ala 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 petition 12–month finding.
Phacelia submutica (DeBeque
phacelia) – We continue to find that
listing this species is warranted-butprecluded 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.
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 petition 12–month 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 10 locations totaling
fewer than 270 wild and outplanted
individuals on State, private, and
Federal lands. Phyllostegia floribunda is
threatened by feral pigs that degrade
and destroy habitat, and nonnative
plants that compete for light and
nutrients. The National Park Service,
The Nature Conservancy, and the State
have outplanted more than 170
individuals at Olaa Forest Reserve, Kona
Hema, and Waiakea Forest Reserve
(more than 50, 20 individuals, and 100
individuals, respectively). Fences
protect approximately five populations
on private, State, and National Park
lands. Nonnative plants have been
reduced in these fenced areas. However,
no conservation efforts have been
implemented for the unfenced
populations. This species is represented
in ex situ collections. Overall, the
threats are moderate because
conservation efforts for over half of the
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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) – See above
in ‘‘Listing Priority Changes in
Candidates.’’ The above 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 (Correll) Leur
(White fringeless orchid) – See above in
‘‘Listing Priority Changes in
Candidates.’’ The above summary is
based on information contained in our
files. No new information was provided
in the petition we received on May 11,
2004.
Platydesma cornuta var. cornuta (no
common name) – We continue to find
that listing this species is warrantedbut-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.
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
petition 12–month 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 two
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
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throughout its limited range. 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 petition 12–month 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
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 as well as
the impacts of past water diversions,
livestock grazing, and off-road 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 and a volunteer site
steward during the 6–month period of
peak visitor use. In California, public
land management actions include
prohibiting livestock salting in the
vicinity of springs, a proposed long-term
monitoring plot, limitations on camping
near springs, withdrawal from salable
mineral leasing, and recommendations
to withdrawal the land from mineral
entry. 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.
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Until a monitoring program is in place
that allows us to assess the long-term
trend of the species, we have assigned
a 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
vegetation in dry consolidated dunes on
Molokai and Maui, Hawaii. This variety
is known from five populations totaling
approximately 10,000 to 20,000
individuals (depending upon rainfall) in
the Moomomi area on the island of
Molokai, and from two 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 and offroad 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 by an ex situ collection. The
ongoing threats from axis deer, cattle,
nonnative plants, collection, and offroad vehicles are of a high magnitude
because no control measures have been
undertaken for the Maui population and
the threats result in direct mortality or
significantly reduce reproductive
capacity for the majority of the
populations. 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
petition 12–month 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 petition 12–month 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.
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Ranunculus hawaiensis is an erect or
ascending perennial herb found in
mesic to wet forest dominated by
Metrosideros polymorpha and Acacia
koa with scree substrate (loose stones or
rocky debris on a slope) on Maui and
the island of Hawaii, Hawaii.
Populations formerly within Haleakala
National Park have been extirpated.
This species is currently known from
fewer than 15 individuals in four
populations: three wild populations
occur on Hawaii totaling 11 individuals,
and a Maui population (Kukui planeze)
which was not relocated on a survey
conducted in 2006. In addition, one
wild population at Waikamoi (on Maui)
was last observed in 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 13
locations totaling fewer than 170
individuals. Ranunculus mauiensis is
threatened by feral pigs, goats, mule
deer and 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 the Maui
populations of R. mauiensis, and
nonnative plants have been reduced in
the fenced areas. One individual occurs
in the Kamakou Preserve on Molokai,
managed by The Nature Conservancy.
However, ongoing conservation efforts
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benefit only the Maui and Molokai
individuals, and absent conservation
efforts for the Kauai individuals, the
threats continue to be of a high
magnitude on Kauai. Therefore, since
half of the individuals are found on
Kauai, threats to the species overall are
also of a high magnitude because these
threats significantly reduce the
reproductive capacity and thus, the
survival of this species. In addition, the
threats are 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
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. 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 ft (1,898 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.
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. Lake levels are expected to
continue to drop in 2009.
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
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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 Understanding/
Conservation 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
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 have maintained 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 Maui, Molokai,
and Hawaii. Currently, this species is
known from six populations totaling
between 29 and 71 individuals on Maui,
from four populations totaling 25
individuals on Molokai, and from one
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 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 three 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
mortaility and reduced reproductive
capacity for the majority of the
populations. 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.
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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 petition 12–month 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
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 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 the 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. Given the high magnitude
and nonimminent threats to the small,
scattered populations of this plant
species, we assigned an LPN of 5 to Red
Mountain stonecrop.
Sicyos macrophyllus (1Anunu) – 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 on the island of
Hawaii, Hawaii. This species is known
from 11 populations totaling fewer than
50 individuals in the Kohala and Mauna
Kea areas and in Hawaii Volcanoes
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National Park (Puna area) on the island
of 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 degrade and destroy
habitat, and 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
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.
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 in Molokai
(approximately 300 plants), the island of
Hawaii (5 plants), and the northwestern
Hawaiian Islands (NWHI): The current
populations in the NWHI are found on:
Midway (approximately 260 plants),
Laysan (approximately 490 plants),
Pearl and Hermes (unknown number of
individuals), 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
northwestern Hawaiian Islands this
species is threatened by nonnative
plants that outcompete and displace it,
and by predation by a nonnative
grasshopper. 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
northwestern Hawaiian Islands. These
threats are of moderate magnitude
because of the relatively large number of
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plants, and 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.
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
on the island of Hawaii, Hawaii.
Stenogyne cranwelliae is known from 11
populations totaling fewer than 100
individuals. This species is threatened
by feral pigs that degrade and destroy
habitat, and nonnative plants that
compete for light and nutrients. In
addition, this species is potentially
threatened by 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 the 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 May 11, 2004.
Georgia aster currently occurs in the
states of Alabama, Georgia, North
Carolina and South Carolina. The
species is presumed extant in three
counties in Alabama, ten counties in
Georgia, nine counties in North
Carolina, and eleven counties in South
Carolina. The species appears to have
been eliminated from Florida.
Georgia aster is a relict species of post
oak savannah/prairie communities that
existed in the southeast prior to
widespread fire suppression and
extirpation of large native grazing
animals. 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
threatened by one or more of the
following factors: woody succession due
to fire suppression, development,
highway expansion/improvement, and
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herbicide application. The threats
described above are currently occurring
and are therefore, imminent. These
threats are expected to operate
throughout the range of the species;
however data on the frequency, timing,
and consequences of these threats are
lacking. Based upon data on other rare
plant species, some of which are
federally listed, occurring in similar
habitats and possessing similar life
histories, we do not currently expect
that these threats are likely to be
irreversible (e.g., to result in the
extirpation of populations) in the near
future. Therefore, the magnitude of
threats is moderate to low. Thus we
assigned an LPN of 8 to 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 petition 12–month 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
streambanks on 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 five
populations totaling 316 individuals.
This species is threatened by feral pigs
that degrade and destroy habitat and
may eat this plant, nonnative plants that
compete for light and nutrients, and
stream diversion. Feral pigs have been
fenced out of the largest population on
Maui, and nonnative 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
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publish prior to making the next annual
resubmitted petition 12–month 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 four populations are known,
totaling 19 to 29 individuals on Hawaii
and Maui. Huperzia stemmermanniae is
threatened by feral pigs, goats, cattle,
and deer that degrade and destroy
habitat, and by nonnative plants that
compete for light, space, and nutrients.
It is also threatened by randomly
occurring natural events due to its small
population size. One individual at
Waikamoi Preserve may benefit from
fencing for deer and pigs. This species
is represented in ex situ collections. The
threats from pigs, goats, cattle, 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. 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. Palapalai is a terrestrial fern found
in mesic to wet forests. It is currently
found on the islands of Maui, Hawaii,
and Oahu, from at least 10 populations
totaling at least 46 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 nonnative
plants that compete for light and
nutrients. Pigs have been fenced out of
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, Hawaii, and Oahu. 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
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capacity. We therefore retained an LPN
of 3 for M. strigosa var. mauiensis.
Petitions To Reclassify Species Already
Listed
We previously made warranted-butprecluded findings on six petitions
seeking to reclassify threatened species
to endangered status. The taxa involved
are three populations of the grizzly bear
(Ursus arctos horribilis), 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
indentified above (see ‘‘Petition
Findings for Candidate Species’’). For
the spikedace, loach minnow, and
Sclerocactus brevispinus, our updated
assessments are provided below. We
find that reclassification to endangered
status for the spikedace, loach minnow,
and Sclerocactus brevispinus is
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, spikedace, loach minnow,
and Sclerocactus brevispinus are
currently listed as threatened, and
therefore already receive certain
protections under the Act. The Service
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
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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–
33894, July 24, 1991; 63 FR 30453–
30454, June 4, 1998), the Cabinet-Yaak
(58 FR 8250–8251, February 12, 1993;
64 FR 26725-26733, May 17, 1999), and
the Selkirk Ecosystems (64 FR 26725–
26733, May 17, 1999). However, none of
these findings included a formal
analysis under our 1996 Policy
Regarding the Recognition of Distinct
Vertebrate Population Segments (DPS)
under the Endangered Species Act (61
FR 4722-4725, February 7, 1996). Under
this policy a formal analysis of
discreteness and significance is
necessary to determine if the petitioned
entity is a ‘‘listable entity’’ and,
therefore, if the petitioned action
remains warranted-but-precluded.
While our 1999 revised 12-month
finding included a preliminary DPS
analysis, it appears to have incorrectly
analyzed significance to the listed entity
(i.e., grizzly bears in the lower 48 States)
instead of significance to the taxon
(Ursus arctos horribilis) as required by
our DPS policy (64 FR 26725–26733,
May 17, 1999; 61 FR 4722-4725,
February 7, 1996; National Association
of Home Builders v. Norton, 340 F. 3d
835, 852 (9th Cir. 2003)). Additionally,
emerging biological information now
suggests increasing levels of
connectivity among some of these
populations casting doubt on their
discreteness.
Also relevant is the March 16, 2007,
Department of the Interior Office of the
Solicitor memorandum (available at:
https://www.doi.gov/solicitor/
M37013.pdf) regarding the meaning of
‘‘significant portion of [a species]
range.’’ This memorandum states that
‘‘whenever the Secretary concludes
because of the statutory five-factor
analysis that a species is ‘in danger of
extinction throughout... a significant
portion of its range,’ it is to be listed and
the protections of the ESA applied to
the species in that portion of its range.’’
The memorandum goes on to say ‘‘the
Secretary has broad discretion in
defining what portion of a range is
‘significant.’ ’’ To date, the Service has
not determined whether the North
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Cascade, the Cabinet-Yaak, or the
Selkirk Ecosystems constitute a
significant portion of the grizzly bear’s
range.
On April 18, 2007, the Service
initiated a 5-year review to evaluate the
current status of grizzly bears in the
lower 48 States outside of the Greater
Yellowstone Area (72 FR 19549-19551).
This status review will fully evaluate
the status of each population and
determine if any of the populations
warrant endangered status. We expect
this 5-year review to be completed in
late 2009.
Spikedace (Meda fulgida) (Region 2)
(see 59 FR 35303, July 11, 1994, and the
species assessment form (see
ADDRESSES) for additional information
on why reclassification to endangered is
warranted-but-precluded) – The
spikedace, a small fish species in a
monotypic genus, is found in moderateto-large perennial waters, where it
inhabits shallow shear zones, sheet
flow, and eddies with sand, gravel, and
rubble substrates, and moderate-to-swift
currents and swift pools over sand or
gravel substrates. This species is now
common only in Aravaipa Creek and
portions of the upper Gila River in New
Mexico. Smaller, less stable populations
occur in some areas of the upper Gila,
and possibly the Verde River. Spikedace
have been translocated into Hot Springs
and Redfield Canyon (San Pedro River
tributaries), Fossil Creek (Verde River
tributary), Bonita Creek (Gila River
tributary), and the San Francisco River
(in New Mexico). Should these
populations become self-sustaining,
they will ultimately contribute to
species recovery.
The threats to this species are
primarily from nonnative aquatic
species and water withdrawals,
including groundwater pumping. Other
threats include improper livestock
grazing, road construction, and
recreation. Spikedace occur in only 5 to
10 percent of their historical range, and
threats occur over the majority of their
range, to varying degrees. Threats are
exacerbated by ongoing drought. In
addition, different threats can interact
with each other to further cause decline.
For example, drought and water
withdrawals may decrease the amount
of habitat available to all species within
a given stream, forcing natives and
nonnatives into closer proximity to one
another. Effects from nonnative species
introductions are permanent, unless
streams are actively renovated and/or
barriers installed to preclude further
recolonization by nonnatives. Grazing
pressures have eased as Federal
agencies remove cattle from streams
directly, but upland conditions continue
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to affect watersheds in general.
Groundwater withdrawals or exchanges
that affect streamflow are not reversible.
For these reasons, the magnitude of the
threat to this species is high. In
addition, most of the threats to this
species are already ongoing, in
particular grazing, water withdrawals,
nonnative stocking programs,
recreational use, and drought. Because
threats have gone on for many years in
the past, are associated with irreversible
commitments (i.e., water exchanges), or
are not easily reversed (i.e., nonnative
stocking and impacts from grazing), the
threats to the species are imminent.
Therefore, we assigned this species an
LPN of 1 for uplisting to endangered.
Loach minnow (Tiaroga cobitis)
(Region 2) (see 59 FR 35303, July 11,
1994, and the species assessment form
(see ADDRESSES) for additional
information on why reclassification to
endangered is warranted-but-precluded)
– This small fish, the only species
within the genus, is found in small-tolarge perennial streams and uses
shallow, turbulent riffles with primarily
cobble substrate and swift currents. This
species is now common only in
Aravaipa Creek and the Blue River in
Arizona, and in limited portions of the
San Francisco, upper Gila, and Tularosa
rivers in New Mexico. Smaller, less
stable populations occur in some areas
of the upper Gila, such as the Middle
Fork and in small areas of several
tributary streams to Aravaipa Creek and
the Blue and Tularosa rivers, such as
Pace, Frieborn, and Negrito creeks.
Small populations are also present in
Eagle Creek and the Black River. Loach
minnow have been translocated into Hot
Springs and Redfield Canyon (San
Pedro River tributaries), Fossil Creek
(Verde River tributary), and Bonita
Creek (Gila River tributary). Should
these populations become selfsustaining, they will ultimately
contribute to species’ recovery.
The threats to this species are
primarily from nonnative aquatic
species and water withdrawals,
including groundwater pumping. Other
threats include improper livestock
grazing, road construction, and
recreation. Loach minnow occur in only
10 to 15 percent of their historical range,
and threats occur over the majority of
their range, to varying degrees. Threats
are exacerbated by ongoing drought. In
addition, different threats can interact
with each other to further cause decline.
For example, drought and water
withdrawals may decrease the amount
of habitat available to all species within
a given stream, bringing natives and
nonnatives into closer contact. Effects
from nonnative species introductions
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are permanent, unless streams are
actively renovated and/or barriers
installed to preclude further
recolonization by nonnatives. Grazing
pressures have eased as Federal
agencies remove cattle from streams
directly, but upland conditions continue
to affect watersheds in general.
Groundwater withdrawals or exchanges
that affect streamflow are not reversible.
For these reasons, the magnitude of the
threats to this species is high. In
addition, most of the threats to this
species are already ongoing, in
particular grazing, water withdrawals,
nonnative stocking programs,
recreational use, and drought. Because
threats have gone on for many years in
the past, are associated with irreversible
commitments (i.e., water exchanges), or
are not easily reversed (i.e., nonnative
stocking and impacts from grazing), the
threats to this species are imminent.
Therefore, we assigned this species an
LPN of 1 for uplisting to endangered.
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 bad-lands 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 is collected as a specimen plant
for horticultural use. Recreational offroad vehicle use and livestock trampling
are additional threats. The species is
currently federally listed as threatened
by its previous inclusion within the
species Sclerocactus glaucus. The
ongoing 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. Thus, we assigned this
species an LPN of 2 for uplisting to
endangered.
Current Notice of Review
We gather data on plants and animals
native to the U.S. 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.
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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
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
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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).
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 December 10, 2008)
that are no longer proposed species or
candidates for listing. Since December
10, 2008, we listed one species and
removed four species from candidate
status for the reasons indicated by the
codes. 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.
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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
‘‘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
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57865
(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 N.E. 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 (505/2486920).
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 551114056 (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
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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 29, 2009
Christine E. Eustis
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
Lead region
Category
Scientific name
Family
Common name
Historical range
Priority
MAMMALS
2
R4
Eumops floridanus
Molossidae
Bat, Florida bonneted
U.S.A. (FL)
C*
3
R1
Emballonura semicaudata
rotensis
Emballonuridae
Bat, Pacific sheath-tailed
(Mariana Islands
subspecies)
U.S.A. (GU,
CNMI)
C*
3
R1
Emballonura semicaudata
semicaudata
Emballonuridae
Bat, Pacific sheath-tailed
(American Samoa DPS)
U.S.A. (AS), Fiji,
Independent
Samoa, Tonga,
Vanuatu
C*
2
R5
Sylvilagus transitionalis
Leporidae
Cottontail, New England
U.S.A. (CT, MA,
ME, NH, NY,
RI, VT)
C*
6
R8
Martes pennanti
Mustelidae
Fisher (west coast DPS)
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
C*
3
R2
Zapus hudsonius luteus
Zapodidae
Mouse, New Mexico
meadow jumping
U.S.A. (AZ, CO,
NM)
C*
3
R1
Thomomys mazama
couchi
Geomyidae
Pocket gopher, Shelton
U.S.A. (WA)
C
3
R1
Thomomys mazama
douglasii
Geomyidae
Pocket gopher,
Brush Prairie
U.S.A. (WA)
C*
3
R1
Thomomys mazama
glacialis
Geomyidae
Pocket gopher, Roy Prairie
U.S.A. (WA)
C*
3
R1
Thomomys mazama louiei
Geomyidae
Pocket gopher, Cathlamet
U.S.A. (WA)
C*
3
R1
Thomomys mazama
melanops
Geomyidae
Pocket gopher, Olympic
U.S.A. (WA)
C*
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C
3
R1
Thomomys mazama
pugetensis
Geomyidae
Pocket gopher, Olympia
U.S.A. (WA)
C*
3
R1
Thomomys mazama
tacomensis
Geomyidae
Pocket gopher, Tacoma
U.S.A. (WA)
C*
3
R1
Thomomys mazama tumuli
Geomyidae
Pocket gopher, Tenino
U.S.A. (WA)
C*
3
R1
Thomomys mazama
yelmensis
Geomyidae
Pocket gopher, Yelm
U.S.A. (WA)
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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
Lead region
Scientific name
Family
Common name
Historical range
Category
Priority
C*
3
R6
Cynomys gunnisoni
Sciuridae
Prairie dog, Gunnison’s
(central and
south-central Colorado,
north-central New
Mexico SPR)
U.S.A. (CO, NM)
C*
3
R8
Spermophilus tereticaudus
chlorus
Sciuridae
Squirrel, Palm Springs (=
Coachella Valley) roundtailed ground
U.S.A. (CA)
C*
9
R1
Spermophilus brunneus
endemicus
Sciuridae
Squirrel, Southern Idaho
ground
U.S.A. (ID)
C*
5
R1
Spermophilus washingtoni
Sciuridae
Squirrel, Washington
ground
U.S.A. (WA, OR)
BIRDS
–
R1
Loxops caeruleirostris
Fringillidae
Akekee (honeycreeper)
U.S.A. (HI)
PE
2
R1
Oreomystis bairdi
Fringillidae
Akikiki (Kauai creeper)
U.S.A. (HI)
C*
3
R1
Porzana tabuensis
Rallidae
Crake, spotless (American
Samoa DPS)
U.S.A. (AS), Australia, Fiji, Independent
Samoa, Marquesas, Philippines, Society
Islands, Tonga
C*
3
R8
Coccyzus americanus
Cuculidae
Cuckoo, yellow-billed
(Western U.S. DPS)
U.S.A. (Lower 48
States), Canada, Mexico,
Central and
South America
C*
9
R1
Gallicolumba stairi
Columbidae
Ground-dove, friendly
(American Samoa DPS)
U.S.A. (AS), Independent Samoa
C*
3
R1
Eremophila alpestris
strigata
Alaudidae
Horned lark, streaked
U.S.A. (OR, WA),
Canada (BC)
C*
3
R5
Calidris canutus rufa
Scolopacidae
Knot, red
U.S.A. (Atlantic
coast), Canada,
South America
C*
8
R7
Gavia adamsii
Gaviidae
Loon, yellow-billed
U.S.A. (AK), Canada, Norway,
Russia, coastal
waters of
southern Pacific and North
Sea
C*
2
R7
Brachyramphus
brevirostris
Alcidae
Murrelet, Kittlitz’s
U.S.A. (AK), Russia.
C*
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PE
5
R8
Synthliboramphus
hypoleucus
Alcidae
Murrelet, Xantus’s
U.S.A. (CA), Mexico
C*
2
R2
Tympanuchus
pallidicinctus
Phasianidae
Prairie-chicken, lesser
U.S.A. (CO, KA,
NM, OK, TX)
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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
Lead region
Scientific name
Family
Common name
Historical range
Category
Priority
C*
6
R1
Centrocercus
urophasianus
Phasianidae
Sage-grouse, greater
(Columbia Basin DPS)
U.S.A. (AZ, CA,
CO, ID, MT,
ND, NE, NV,
OR, SD, UT,
WA, WY), Canada (AB, BC,
SK)
C*
3
R1
Oceanodroma castro
Hydrobatidae
Storm-petrel, band-rumped
(Hawaii DPS)
U.S.A. (HI), Atlantic Ocean, Ecuador (Galapagos Islands),
Japan
C*
11
R4
Dendroica angelae
Emberizidae
Warbler, elfin-woods
U.S.A. (PR)
REPTILES
C*
3
R2
Thamnophis eques
megalops
Colubridae
Gartersnake, northern
Mexican
U.S.A. (AZ, NM,
NV), Mexico
C*
2
R2
Sceloporus arenicolus
Iguanidae
Lizard, sand dune
U.S.A. (TX, NM)
C*
9
R3
Sistrurus catenatus
catenatus
Viperidae
Massasauga
(=rattlesnake), eastern
U.S.A. (IA, IL, IN,
MI, MO, MN,
NY, OH, PA,
WI), Canada
C*
3
R4
Pituophis melanoleucus
lodingi
Colubridae
Snake, black pine
U.S.A. (AL, LA,
MS)
C*
5
R4
Pituophis ruthveni
Colubridae
Snake, Louisiana pine
U.S.A. (LA, TX)
C*
3
R2
Kinosternon sonoriense
longifemorale
Kinosternidae
Turtle, Sonoyta mud
U.S.A. (AZ), Mexico
AMPHIBIANS
9
R8
Rana luteiventris
Ranidae
Frog, Columbia spotted
(Great Basin DPS)
U.S.A. (AK, ID,
MT, NV, OR,
UT, WA, WY),
Canada (BC)
C*
3
R8
Rana muscosa
Ranidae
Frog, mountain yellowlegged (Sierra Nevada
DPS)
U.S.A (CA, NV)
C*
2
R1
Rana pretiosa
Ranidae
Frog, Oregon spotted
U.S.A. (CA, OR,
WA), Canada
(BC)
C*
11
R8
Rana onca
Ranidae
Frog, relict leopard
U.S.A. (AZ, NV,
UT)
C*
3
R3
Cryptobranchus
alleganiensis bishopi
Crytobranchidae
Hellbender, Ozark
U.S.A. (AR, MO)
C*
jlentini on DSKJ8SOYB1PROD with PROPOSALS3
C*
2
R2
Eurycea waterlooensis
Plethodontidae
Salamander, Austin blind
U.S.A. (TX)
C*
8
R2
Eurycea naufragia
Plethodontidae
Salamander, Georgetown
U.S.A. (TX)
C*
8
R2
Eurycea tonkawae
Plethodontidae
Salamander, Jollyville
Plateau
U.S.A. (TX)
C*
2
R2
Eurycea chisholmensis
Plethodontidae
Salamander, Salado
U.S.A. (TX)
C*
11
R8
Bufo canorus
Bufonidae
Toad, Yosemite
U.S.A. (CA)
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Note: See end of SUPPLEMENTARY INFORMATION for an explanation of symbols used in this table.
Status
Lead region
Scientific name
3
R2
8
R4
Necturus alabamensis
Historical range
Treefrog, Arizona
(Huachuca/Canelo DPS)
U.S.A. (AZ), Mexico (Sonora)
Proteidae
Hyla wrightorum
C*
Family
Waterdog, black warrior
(=Sipsey Fork)
U.S.A. (AL)
Priority
C
Common name
Hylidae
Category
FISHES
C*
8
R2
Gila nigra
Cyprinidae
Chub, headwater
U.S.A. (AZ, NM)
C*
9
R2
Gila robusta
Cyprinidae
Chub, roundtail (Lower
Colorado River Basin
DPS)
U.S.A. (AZ, CO,
NM, UT, WY)
C
5
R4
Phoxinus saylori
Cyprinidae
Dace, laurel
U.S.A. (TN)
C*
11
R6
Etheostoma cragini
Percidae
Darter, Arkansas
U.S.A. (AR, CO,
KS, MO, OK)
C*
5
R4
Etheostoma susanae
Percidae
Darter, Cumberland
U.S.A. (KY, TN)
C
2
R5
Crystallaria cincotta
Percidae
Darter, diamond
U.S.A. (KY, OH,
TN, WV)
C*
8
R4
Percina aurora
Percidae
Darter, Pearl
U.S.A. (LA, MS)
C*
2
R4
Etheostoma phytophilum
Percidae
Darter, rush
U.S.A. (AL)
C*
2
R4
Etheostoma moorei
Percidae
Darter, yellowcheek
U.S.A (AR)
C*
2
R4
Noturus crypticus
Ictaluridae
Madtom, chucky
U.S.A. (TN)
C
5
R4
Moxostoma sp.
Catostomidae
Redhorse, sicklefin
U.S.A. (GA, NC,
TN)
C*
2
R3
Cottus sp.
Cottidae
Sculpin, grotto
U.S.A. (MO)
C*
5
R2
Notropis oxyrhynchus
Cyprinidae
Shiner, sharpnose
U.S.A. (TX)
C*
5
R2
Notropis buccula
Cyprinidae
Shiner, smalleye
U.S.A. (TX)
C*
3
R2
Catostomus discobolus
yarrowi
Catostomidae
Sucker, Zuni bluehead
U.S.A. (AZ, NM)
PSAT
N/A
R1
Salvelinus malma
Salmonidae
Trout, Dolly Varden
U.S.A. (AK, WA),
Canada, East
Asia
C*
9
R2
Oncorhynchus clarki
virginalis
Salmonidae
Trout, Rio Grande
cutthroat
U.S.A. (CO, NM)
CLAMS
5
R4
Villosa choctawensis
Unionidae
Bean, Choctaw
U.S.A. (AL, FL)
C
jlentini on DSKJ8SOYB1PROD with PROPOSALS3
C
2
R3
Villosa fabalis
Unionidae
Bean, rayed
U.S.A. (IL, IN,
KY, MI, NY,
OH, TN, PA,
VA, WV), Canada (ON)
C
2
R4
Fusconaia rotulata
Unionidae
Ebonyshell, round
U.S.A. (AL, FL)
C*
8
R2
Popenaias popei
Unionidae
Hornshell, Texas
U.S.A. (NM, TX),
Mexico
C*
2
R4
Ptychobranchus subtentum
Unionidae
Kidneyshell, fluted
U.S.A. (AL, KY,
TN, VA)
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Note: See end of SUPPLEMENTARY INFORMATION for an explanation of symbols used in this table.
Status
Lead region
Scientific name
Family
Common name
Historical range
Category
Priority
C
2
R4
Ptychobranchus jonesi
Unionidae
Kidneyshell, southern
U.S.A. (AL, FL)
C*
2
R4
Lampsilis rafinesqueana
Unionidae
Mucket, Neosho
U.S.A. (AR, KS,
MO, OK)
C
2
R3
Plethobasus cyphyus
Unionidae
Mussel, sheepnose
U.S.A. (AL, IA, IL,
IN, KY, MN,
MO, MS, OH,
PA, TN, VA,
WI, WV)
C*
2
R4
Margaritifera marrianae
Margaritiferidae
Pearlshell, Alabama
U.S.A. (AL)
C*
2
R4
Lexingtonia dolabelloides
Unionidae
Pearlymussel, slabside
U.S.A. (AL, KY,
TN, VA)
C
5
R4
Pleurobema strodeanum
Unionidae
Pigtoe, fuzzy
U.S.A. (AL, FL)
PE
2
R4
Pleurobema hanleyianum
Unionidae
Pigtoe, Georgia
U.S.A. (AL, GA,
TN)
C
5
R4
Fusconaia escambia
Unionidae
Pigtoe, narrow
U.S.A. (AL, FL)
C
11
R4
Fusconaia (=Quincuncina)
burkei
Unionidae
Pigtoe, tapered
U.S.A. (AL, FL)
C
9
R4
Quadrula cylindrica
cylindrica
Unionidae
Rabbitsfoot
U.S.A. (AL, AR,
GA, IN, IL, KS,
KY, LA, MS,
MO, OK, OH,
PA, TN, WV)
C
5
R4
Hamiota (=Lampsilis)
australis
Unionidae
Sandshell, southern
U.S.A. (AL, FL)
C
4
R3
Cumberlandia monodonta
Margaritiferidae
Spectaclecase
U.S.A. (AL, AR,
IA, IN, IL, KS,
KY, MO, MN,
NE, OH, TN,
VA, WI, WV)
C*
2
R4
Elliptio spinosa
Unionidae
Spinymussel, Altamaha
U.S.A. (GA)
SNAILS
2
R4
Pleurocera foremani
Pleuroceridae
Hornsnail, rough
U.S.A. (AL)
C
8
R4
Elimia melanoides
Pleuroceridae
Mudalia, black
U.S.A. (AL)
PE
2
R4
Leptoxis foremani (=
downei)
Pleuroceridae
Rocksnail, Interrupted (=
Georgia)
U.S.A. (GA, AL)
C*
2
R1
Ostodes strigatus
Potaridae
Sisi snail
U.S.A. (AS)
C*
2
R2
Pseudotryonia adamantina
Hydrobiidae
Snail, Diamond Y Spring
U.S.A. (TX)
C*
2
R1
Samoana fragilis
Partulidae
Snail, fragile tree
U.S.A. (GU, MP)
C*
jlentini on DSKJ8SOYB1PROD with PROPOSALS3
PE
2
R1
Partula radiolata
Partulidae
Snail, Guam tree
U.S.A. (GU)
C*
2
R1
Partula gibba
Partulidae
Snail, Humped tree
U.S.A. (GU, MP)
C*
2
R1
Partulina semicarinata
Achatinellidae
Snail, Lanai tree
U.S.A. (HI)
C*
2
R1
Partulina variabilis
Achatinellidae
Snail, Lanai tree
U.S.A. (HI)
C*
2
R1
Partula langfordi
Partulidae
Snail, Langford’s tree
U.S.A. (MP)
C*
2
R2
Cochliopa texana
Hydrobiidae
Snail, Phantom cave
U.S.A. (TX)
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Note: See end of SUPPLEMENTARY INFORMATION for an explanation of symbols used in this table.
Status
Lead region
Scientific name
Family
Common name
Historical range
Category
Priority
C*
2
R1
Newcombia cumingi
Achatinellidae
Snail, Newcomb’s tree
U.S.A. (Hl)
C*
2
R1
Eua zebrina
Partulidae
Snail, Tutuila tree
U.S.A. (AS)
C*
2
R2
Pyrgulopsis chupaderae
Hydrobiidae
Springsnail, Chupadera
U.S.A. (NM)
C*
11
R8
Pyrgulopsis notidicola
Hydrobiidae
Springsnail, elongate mud
meadows
U.S.A. (NV)
C*
11
R2
Pyrgulopsis gilae
Hydrobiidae
Springsnail, Gila
U.S.A. (NM)
C*
2
R2
Tryonia circumstriata
(=stocktonensis)
Hydrobiidae
Springsnail, Gonzales
U.S.A. (TX)
C*
8
R2
Pyrgulopsis thompsoni
Hydrobiidae
Springsnail, Huachuca
U.S.A. (AZ), Mexico
C*
11
R2
Pyrgulopsis thermalis
Hydrobiidae
Springsnail, New Mexico
U.S.A. (NM)
C*
2
R2
Pyrgulopsis morrisoni
Hydrobiidae
Springsnail, Page
U.S.A. (AZ)
C*
2
R2
Tryonia cheatumi
Hydrobiidae
Springsnail (=Tryonia),
Phantom
U.S.A. (TX)
C
2
R2
Pyrgulopsis bernardina
Hydrobiidae
Springsnail, San
Bernardino
U.S.A. (AZ), Mexico (Sonora)
C*
2
R2
Pyrgulopsis trivialis
Hydrobiidae
Springsnail, Three Forks
U.S.A. (AZ)
INSECTS
8
R1
Nysius wekiuicola
Lygaeidae
Bug, Wekiu
U.S.A. (HI)
C
3
R4
Strymon acis bartrami
Lycaenidae
Butterfly, Bartram’s
hairstreak
U.S.A. (FL)
C
3
R4
Anaea troglodyta floridalis
Nymphalidae
Butterfly, Florida leafwing
U.S.A. (FL)
C*
3
R1
Hypolimnas octucula
mariannensis
Nymphalidae
Butterfly, Mariana eightspot
U.S.A. (GU, MP)
C*
2
R1
Vagrans egistina
Nymphalidae
Butterfly, Mariana
wandering
U.S.A. (GU, MP)
C*
3
R4
Cyclargus thomasi
bethunebakeri
Lycaenidae
Butterfly, Miami blue
U.S.A. (FL), Bahamas
C*
5
R4
Glyphopsyche sequatchie
Limnephilidae
Caddisfly, Sequatchie
U.S.A. (TN)
C
5
R4
Pseudanophthalmus
insularis
Carabidae
Cave beetle, Baker Station
(= insular)
U.S.A. (TN)
C*
5
R4
Pseudanophthalmus
caecus
Carabidae
Cave beetle, Clifton
U.S.A. (KY)
C
11
R4
Pseudanophthalmus
colemanensis
Carabidae
Cave beetle, Coleman
U.S.A. (TN)
C
jlentini on DSKJ8SOYB1PROD with PROPOSALS3
C*
5
R4
Pseudanophthalmus
fowlerae
Carabidae
Cave beetle, Fowler’s
U.S.A. (TN)
C*
5
R4
Pseudanophthalmus
frigidus
Carabidae
Cave beetle, icebox
U.S.A. (KY)
C
5
R4
Pseudanophthalmus
tiresias
Carabidae
Cave beetle, Indian Grave
Point (= Soothsayer)
U.S.A. (TN)
C*
5
R4
Pseudanophthalmus
inquisitor
Carabidae
Cave beetle, inquirer
U.S.A. (TN)
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Note: See end of SUPPLEMENTARY INFORMATION for an explanation of symbols used in this table.
Status
Lead region
Scientific name
Family
Common name
Historical range
Category
Priority
C*
5
R4
Pseudanophthalmus
troglodytes
Carabidae
Cave beetle, Louisville
U.S.A. (KY)
C
5
R4
Pseudanophthalmus
paulus
Carabidae
Cave beetle, Noblett’s
U.S.A. (TN).
C*
5
R4
Pseudanophthalmus
parvus
Carabidae
Cave beetle, Tatum
U.S.A. (KY)
C*
3
R1
Euphydryas editha taylori
Nymphalidae
Checkerspot butterfly,
Taylor’s (= Whulge)
U.S. A. (OR,
WA), Canada
(BC)
C*
9
R1
Megalagrion
nigrohamatum
nigrolineatum
Coenagrionidae
Damselfly, blackline Hawaiian
U.S.A. (HI)
C*
2
R1
Megalagrion leptodemas
Coenagrionidae
Damselfly, crimson Hawaiian
U.S.A. (HI)
PE
2
R1
Megalagrion nesiotes
Coenagrionidae
Damselfly, flying earwig
Hawaiian
U.S.A. (HI)
C*
2
R1
Megalagrion oceanicum
Coenagrionidae
Damselfly, oceanic Hawaiian
U.S.A. (HI)
C*
8
R1
Megalagrion xanthomelas
Coenagrionidae
Damselfly, orangeblack
Hawaiian
U.S.A. (HI)
PE
2
R1
Megalagrion pacificum
Coenagrionidae
Damselfly, Pacific
Hawaiian
U.S.A. (HI)
PE
2
R8
Dinacoma caseyi
Scarabidae
June beetle, Casey’s
U.S.A. (CA)
C
5
R8
Ambrysus funebris
Naucoridae
Naucorid bug (=Furnace
Creek), Nevares Spring
U.S.A. (CA)
PE
2
R1
Drosophila attigua
Drosophilidae
fly, Hawaiian picture-wing
U.S.A. (HI)
C*
2
R1
Drosophila digressa
Drosophilidae
fly, Hawaiian Picture-wing
U.S.A. (HI)
C*
8
R2
Heterelmis stephani
Elmidae
Riffle beetle, Stephan’s
U.S.A. (AZ)
C*
8
R3
Hesperia dacotae
Hesperiidae
Skipper, Dakota
U.S.A. (MN, IA,
SD, ND, IL),
Canada
C*
8
R1
Polites mardon
Hesperiidae
Skipper, Mardon
U.S.A. (CA, OR,
WA)
C*
2
R6
Cicindela albissima
Cicindelidae
Tiger beetle, Coral Pink
Sand Dunes
U.S.A. (UT)
C*
5
R4
Cicindela highlandensis
Cicindelidae
Tiger beetle, highlands
U.S.A. (FL)
Meshweaver, Warton’s
cave
U.S.A. (TX)
ARACHNIDS
jlentini on DSKJ8SOYB1PROD with PROPOSALS3
C*
2
R2
Cicurina wartoni
Dictynidae
CRUSTACEANS
C
2
R2
Gammarus hyalleloides
Gammaridae
Amphipod, diminutive
U.S.A. (TX)
C*
5
R1
Metabetaeus lohena
Alpheidae
Shrimp, anchialine pool
U.S.A. (HI)
C*
5
R1
Palaemonella burnsi
Palaemonidae
Shrimp, anchialine pool
U.S.A. (HI)
C*
5
R1
Procaris hawaiana
Procarididae
Shrimp, anchialine pool
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
Lead region
Category
C*
4
Scientific name
Family
Common name
Historical range
Priority
R1
Vetericaris chaceorum
Procaridae
Shrimp, anchialine pool
U.S.A. (HI)
FLOWERING PLANTS
11
R8
Abronia alpina
Nyctaginaceae
Sand-verbena, Ramshaw
Meadows
U.S.A. (CA)
C*
8
R4
Arabis georgiana
Brassicaceae
Rockcress, Georgia
U.S.A. (AL, GA)
C*
11
R4
Argythamnia blodgettii
Euphorbiaceae
Silverbush, Blodgett’s
U.S.A. (FL)
C*
3
R1
Artemisia campestris var.
wormskioldii
Asteraceae
Wormwood, northern
U.S.A. (OR, WA)
PE
2
R1
Astelia waialealae
Liliaceae
Pa1iniu
U.S.A. (HI)
C*
5
R1
Astragalus anserinus
Fabaceae
Milkvetch, Goose Creek
U.S.A. (ID, NV,
UT)
C*
11
R6
Astragalus tortipes
Fabaceae
Milkvetch, Sleeping Ute
U.S.A. (CO)
C*
2
R1
Bidens amplectens
Asteraceae
Ko1oko1olau
U.S.A. (HI)
C*
3
R1
Bidens campylotheca
pentamera
Asteraceae
Ko1oko1olau
U.S.A. (HI)
C*
3
R1
Bidens campylotheca
waihoiensis
Asteraceae
Ko1oko1olau
U.S.A. (HI)
C*
8
R1
Bidens conjuncta
Asteraceae
Ko1oko1olau
U.S.A. (HI)
C*
3
R1
Bidens micrantha
ctenophylla
Asteraceae
Ko1oko1olau
U.S.A. (HI)
C*
8
R4
Brickellia mosieri
Asteraceae
Brickell-bush, Florida
U.S.A. (FL)
C*
2
R1
Calamagrostis expansa
Poaceae
Reedgrass, Maui
U.S.A. (HI)
C*
2
R1
Calamagrostis hillebrandii
Poaceae
Reedgrass, Hillebrand’s
U.S.A. (HI)
C*
5
R8
Calochortus persistens
Liliaceae
Mariposa lily, Siskiyou
U.S.A. (CA, OR)
PE
2
R1
Canavalia napaliensis
Fabaceae
1Awikiwiki
U.S.A. (HI)
C*
2
R1
Canavalia pubescens
Fabaceae
1Awikiwiki
U.S.A. (HI)
C*
8
R1
Castilleja christii
Scrophulariaceae
Paintbrush, Christ’s
U.S.A. (ID)
C*
9
R4
Chamaecrista lineata var.
keyensis
Fabaceae
Pea, Big Pine partridge
U.S.A. (FL)
C*
12
R4
Chamaesyce deltoidea
pinetorum
Euphorbiaceae
Sandmat, pineland
U.S.A. (FL)
C*
9
R4
Chamaesyce deltoidea
serpyllum
Euphorbiaceae
Spurge, wedge
U.S.A. (FL)
PE
2
R1
Chamaesyce eleanoriae
Euphorbiaceae
1Akoko
U.S.A. (HI)
PE
jlentini on DSKJ8SOYB1PROD with PROPOSALS3
C*
3
R1
Chamaesyce remyi var.
kauaiensis
Euphorbiaceae
1Akoko
U.S.A. (HI)
PE
3
R1
Chamaesyce remyi var.
remyi
Euphorbiaceae
1Akoko
U.S.A. (HI)
PE
2
R1
Charpentiera densiflora
Amaranthaceae
Papala
U.S.A. (HI)
C*
6
R8
Chorizanthe parryi var.
fernandina
Polygonaceae
Spineflower, San Fernando Valley
U.S.A. (CA)
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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
Lead region
Scientific name
Family
Common name
Historical range
Priority
C*
2
R4
Chromolaena frustrata
Asteraceae
Thoroughwort, Cape Sable
U.S.A. (FL)
C*
2
R4
Consolea corallicola
Cactaceae
Cactus, Florida semaphore
U.S.A. (FL)
C*
5
R4
Cordia rupicola
Boraginaceae
No common name
U.S.A. (PR),
Anegada
C*
2
R1
Cyanea asplenifolia
Campanulaceae
Haha
U.S.A. (HI)
C*
2
R1
Cyanea calycina
Campanulaceae
Haha
U.S.A. (HI)
PE
–
R1
Cyanea dolichopoda
Campanulaceae
Haha
U.S.A. (HI)
PE
2
R1
Cyanea eleeleensis
Campanulaceae
Haha
U.S.A. (HI)
PE
–
R1
Cyanea kolekoleensis
Campanulaceae
Haha
U.S.A. (HI)
PE
2
R1
Cyanea kuhihewa
Campanulaceae
Haha
U.S.A. (HI)
C*
2
R1
Cyanea kunthiana
Campanulaceae
Haha
U.S.A. (HI)
C*
2
R1
Cyanea lanceolata
Campanulaceae
Haha
U.S.A. (HI)
C*
2
R1
Cyanea obtusa
Campanulaceae
Haha
U.S.A. (HI)
C*
2
R1
Cyanea tritomantha
Campanulaceae
1Aku
U.S.A. (HI)
C*
2
R1
Cyrtandra filipes
Gesneriaceae
Ha1iwale
U.S.A. (HI)
C*
2
R1
Cyrtandra kaulantha
Gesneriaceae
Ha1iwale
U.S.A. (HI)
PE
2
R1
Cyrtandra oenobarba
Gesneriaceae
Ha1iwale
U.S.A. (HI)
C*
2
R1
Cyrtandra oxybapha
Gesneriaceae
Ha1iwale
U.S.A. (HI)
PE
–
R1
Cyrtandra paliku
Gesneriaceae
Ha1iwale
U.S.A. (HI)
C*
2
R1
Cyrtandra sessilis
Gesneriaceae
Ha1iwale
U.S.A. (HI)
C*
3
R4
Dalea carthagenensis var.
floridana
Fabaceae
Prairie-clover, Florida
U.S.A. (FL)
C*
5
R5
Dichanthelium hirstii
Poaceae
Panic grass, Hirsts’
U.S.A. (DE, GA,
NC, NJ)
C*
5
R4
Digitaria pauciflora
Poaceae
Crabgrass, Florida
pineland
U.S.A. (FL)
PE
3
R1
Dubautia imbricata
imbricata
Asteraceae
Na1ena1e
U.S.A. (HI)
PE
–
R1
Dubautia kalalauensis
Asteraceae
Na1ena1e
U.S.A. (HI)
PE
–
R1
Dubautia kenwoodii
Asteraceae
Na1ena1e
U.S.A. (HI)
PE
3
R1
Dubautia plantaginea
magnifolia
Asteraceae
Na1ena1e
U.S.A. (HI)
PE
jlentini on DSKJ8SOYB1PROD with PROPOSALS3
Category
2
R1
Dubautia waialealae
Asteraceae
Na1ena1e
U.S.A. (HI)
C*
3
R2
Echinomastus
erectocentrus var.
acunensis
Cactaceae
Cactus, Acuna
U.S.A. (AZ), Mexico
C*
8
R2
Erigeron lemmonii
Asteraceae
Fleabane, Lemmon
U.S.A. (AZ)
C*
2
R1
Eriogonum codium
Polygonaceae
Buckwheat, Umtanum
Desert
U.S.A. (WA)
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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
Lead region
Scientific name
Family
Common name
Historical range
Priority
C*
6
R8
Eriogonum corymbosum
var. nilesii
Polygonaceae
Buckwheat, Las Vegas
U.S.A. (NV)
C
5
R8
Eriogonum diatomaceum
Polygonaceae
Buckwheat, Churchill
Narrows
U.S.A (NV)
C*
5
R8
Eriogonum kelloggii
Polygonaceae
Buckwheat, Red Mountain
U.S.A. (CA)
C*
2
R1
Festuca hawaiiensis
Poaceae
No common name
U.S.A. (HI)
C*
11
R2
Festuca ligulata
Poaceae
Fescue, Guadalupe
U.S.A. (TX), Mexico
C*
2
R1
Gardenia remyi
Rubiaceae
Nanu
U.S.A. (HI)
C*
8
R1
Geranium hanaense
Geraniaceae
Nohoanu
U.S.A. (HI)
C*
8
R1
Geranium hillebrandii
Geraniaceae
Nohoanu
U.S.A. (HI)
PE
5
R1
Geranium kauaiense
Geraniaceae
Nohoanu
U.S.A. (HI)
C*
5
R4
Gonocalyx concolor
Ericaceae
No common name
U.S.A. (PR)
C
2
R4
Harrisia aboriginum
Cactaceae
Pricklyapple, aboriginal
(shellmound
applecactus)
U.S.A. (FL)
C*
5
R8
Hazardia orcuttii
Asteraceae
Orcutt’s hazardia
U.S.A. (CA), Mexico
C*
2
R1
Hedyotis fluviatilis
Rubiaceae
Kampua1a
U.S.A. (HI)
C*
8
R4
Helianthus verticillatus
Asteraceae
Sunflower, whorled
U.S.A. (AL, GA,
TN)
C*
5
R2
Hibiscus dasycalyx
Malvaceae
Rose-mallow, Neches
River
U.S.A. (TX)
C
2
R6
Ipomopsis polyantha
Polemoniaceae
Skyrocket, Pagosa
U.S.A. (CO)
C*
5
R8
Ivesia webberi
Rosaceae
Ivesia, Webber
U.S.A. (CA, NV)
C*
3
R1
Joinvillea ascendens
ascendens
Joinvilleaceae
1Ohe
U.S.A. (HI)
PE
2
R1
Keysseria erici
Asteraceae
No common name
U.S.A. (HI)
PE
8
R1
Keysseria helenae
Asteraceae
No common name
U.S.A. (HI)
C*
2
R1
Korthalsella degeneri
Viscaceae
Hulumoa
U.S.A. (HI)
PE
2
R1
Labordia helleri
Loganiaceae
Kamakahala
U.S.A. (HI)
PE
2
R1
Labordia pumila
Loganiaceae
Kamakahala
U.S.A. (HI)
C*
5
R4
Leavenworthia crassa
Brassicaceae
Gladecress, unnamed
U.S.A. (AL)
C
jlentini on DSKJ8SOYB1PROD with PROPOSALS3
Category
3
R4
Leavenworthia exigua var.
laciniata
Brassicaceae
Gladecress, Kentucky
U.S.A. (KY)
C*
2
R2
Leavenworthia texana
Brassicaceae
Gladecress, Texas golden
U.S.A. (TX)
PE
–
R1
Lepidium papilliferum
Brassicaceae
Peppergrass, slickspot
U.S.A. (ID)
C*
8
R4
Lesquerella globosa
Brassicaceae
Bladderpod, Short’s
U.S.A. (IN, KY,
TN)
C*
2
R4
Linum arenicola
Linaceae
Flax, sand
U.S.A. (FL)
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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
Lead region
Scientific name
Family
Common name
Historical range
Priority
C*
3
R4
Linum carteri var. carteri
Linaceae
Flax, Carter’s smallflowered
U.S.A. (FL)
PE
8
R1
Lysimachia daphnoides
Myrsinaceae
Lehua makanoe
U.S.A. (HI)
PE
–
R1
Lysimachia iniki
Myrsinaceae
No common name
U.S.A. (HI)
PE
–
R1
Lysimachia pendens
Myrsinaceae
No common name
U.S.A. (HI)
PE
–
R1
Lysimachia scopulensis
Myrsinaceae
No common name
U.S.A. (HI)
PE
–
R1
Lysimachia venosa
Myrsinaceae
No common name
U.S.A. (HI)
C*
2
R1
Melicope christophersenii
Rutaceae
Alani
U.S.A. (HI)
PE
2
R1
Melicope degeneri
Rutaceae
Alani
U.S.A. (HI)
C*
2
R1
Melicope hiiakae
Rutaceae
Alani
U.S.A. (HI)
C*
2
R1
Melicope makahae
Rutaceae
Alani
U.S.A. (HI)
PE
2
R1
Melicope paniculata
Rutaceae
Alani
U.S.A. (HI)
PE
2
R1
Melicope puberula
Rutaceae
Alani
U.S.A. (HI)
C*
2
R1
Myrsine fosbergii
Myrsinaceae
Kolea
U.S.A. (HI)
PE
–
R1
Myrsine knudsenii
Myrsinaceae
Kolea
U.S.A. (HI)
PE
2
R1
Myrsine mezii
Myrsinaceae
Kolea
U.S.A. (HI)
C*
2
R1
Myrsine vaccinioides
Myrsinaceae
Kolea
U.S.A. (HI)
C*
8
R5
Narthecium americanum
Liliaceae
Asphodel, bog
U.S.A. (DE, NC,
NJ, NY, SC)
C*
2
R1
Nothocestrum latifolium
Solanaceae
1Aiea
U.S.A. (HI)
C*
2
R1
Ochrosia haleakalae
Apocynaceae
Holei
U.S.A. (HI)
C*
3
R2
Pediocactus peeblesianus
var. fickeiseniae
Cactaceae
Cactus, Fickeisen plains
U.S.A. (AZ)
C*
2
R6
Penstemon debilis
Scrophulariaceae
Beardtongue, Parachute
U.S.A. (CO)
C*
6
R6
Penstemon scariosus var.
albifluvis
Scrophulariaceae
Beardtongue, White River
U.S.A. (CO, UT)
C*
2
R1
Peperomia subpetiolata
Piperaceae
1Ala 1ala wai nui
U.S.A. (HI)
C
5
R8
Phacelia stellaris
Hydrophyllaceae
Phacelia, Brand’s
U.S.A. (CA), Mexico
C*
8
R6
Phacelia submutica
Hydrophyllaceae
Phacelia, DeBeque
U.S.A. (CO)
C*
2
R1
Phyllostegia bracteata
Lamiaceae
No common name
U.S.A. (HI)
C*
8
R1
Phyllostegia floribunda
Lamiaceae
No common name
U.S.A. (HI)
PE
jlentini on DSKJ8SOYB1PROD with PROPOSALS3
Category
–
R1
Phyllostegia renovans
Lamiaceae
No common name
U.S.A. (HI)
C*
9
R1
Physaria douglasii
tuplashensis
Brassicaceae
Bladderpod, White Bluffs
U.S.A. (WA)
PE
2
R1
Pittosporum napaliense
Pittosporaceae
Ho1awa
U.S.A. (HI)
C*
8
R4
Platanthera integrilabia
Orchidaceae
Orchid, white fringeless
U.S.A. (AL, GA,
KY, MS, NC,
SC, TN, VA)
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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
Lead region
Scientific name
Family
Common name
Historical range
Priority
C*
3
R1
Platydesma cornuta var.
cornuta
Rutaceae
No common name
U.S.A. (HI)
C*
3
R1
Platydesma cornuta var.
decurrens
Rutaceae
No common name
U.S.A. (HI)
C*
2
R1
Platydesma remyi
Rutaceae
No common name
U.S.A. (HI)
PE
2
R1
Platydesma rostrata
Rutaceae
Pilo kea lau li1i
U.S.A. (HI)
C
2
R1
Pleomele fernaldii
Agavaceae
Hala pepe
U.S.A. (HI)
C*
2
R1
Pleomele forbesii
Agavaceae
Hala pepe
U.S.A. (HI)
C*
11
R8
Potentilla basaltica
Rosaceae
Cinquefoil, Soldier
Meadow
U.S.A. (NV)
PE
2
R1
Pritchardia hardyi
Asteraceae
Lo1ulu
U.S.A. (HI)
C*
3
R1
Pseudognaphalium
(=Gnaphalium)
sandwicensium var.
molokaiense
Asteraceae
1Ena1ena
U.S.A. (HI)
PE
2
R1
Psychotria grandiflora
Rubiaceae
Kopiko
U.S.A. (HI)
C*
3
R1
Psychotria hexandra ssp.
oahuensis var.
oahuensis
Rubiaceae
Kopiko
U.S.A. (HI)
PE
2
R1
Psychotria hobdyi
Rubiaceae
Kopiko
U.S.A. (HI)
C*
2
R1
Pteralyxia macrocarpa
Apocynaceae
Kaulu
U.S.A. (HI)
C*
2
R1
Ranunculus hawaiensis
Ranunculaceae
Makou
U.S.A. (HI)
C*
2
R1
Ranunculus mauiensis
Ranunculaceae
Makou
U.S.A. (HI)
C*
8
R8
Rorippa subumbellata
Brassicaceae
Cress, Tahoe yellow
U.S.A. (CA, NV)
PE
2
R1
Schiedea attenuata
Caryophyllaceae
No common name
U.S.A. (HI)
C*
2
R1
Schiedea pubescens
Caryophyllaceae
Ma1oli1oli
U.S.A. (HI)
C*
2
R1
Schiedea salicaria
Caryophyllaceae
No common name
U.S.A. (HI)
C*
5
R8
Sedum eastwoodiae
Crassulaceae
Stonecrop, Red Mountain
U.S.A. (CA)
C*
2
R1
Sicyos macrophyllus
Cucurbitaceae
1Anunu
U.S.A. (HI)
C
12
R4
Sideroxylon reclinatum
austrofloridense
Sapotaceae
Bully, Everglades
U.S.A. (FL)
C*
8
R1
Solanum nelsonii
Solanaceae
Popolo
U.S.A. (HI)
C
8
R4
Solidago plumosa
Asteraceae
Goldenrod, Yadkin River
U.S.A. (NC)
C
2
R2
Sphaeralcea gierischii
Malvaceae
Mallow, Gierisch
U.S.A. (AZ, UT)
C*
jlentini on DSKJ8SOYB1PROD with PROPOSALS3
Category
2
R1
Stenogyne cranwelliae
Lamiaceae
No common name
U.S.A. (HI)
PE
2
R1
Stenogyne kealiae
Lamiaceae
No common name
U.S.A. (HI)
C*
8
R4
Symphyotrichum
georgianum
Asteraceae
Aster, Georgia
U.S.A. (AL, FL,
GA, NC, SC)
PE
–
R1
Tetraplasandra
bisattenuata
Araliaceae
No common name
U.S.A. (HI)
PE
–
R1
Tetraplasandra flynnii
Araliaceae
No common name
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
Lead region
Category
C*
2
Scientific name
Family
Common name
Historical range
Priority
R1
Zanthoxylum oahuense
Rutaceae
A1e
U.S.A. (HI)
FERNS AND ALLIES
C*
8
R1
Christella boydiae (=
Cyclosorus boydiae var.
boydiae + Cyclosorus
boydiae kipahuluensis)
Thelypteridaceae
No common name
U.S.A. (HI)
PE
–
R1
Diellia mannii
Aspleniaceae
No common name
U.S.A. (HI)
PE
–
R1
Doryopteris angelica
Pteridaceae
No common name
U.S.A. (HI)
C*
2
R1
Doryopteris takeuchii
Pteridaceae
No common name
U.S.A. (HI)
PE
–
R1
Dryopteris crinalis var.
podosorus
Dryopteridaceae
Palapalai aumakua
U.S.A. (HI)
C*
2
R1
Huperzia (=
Phlegmariurus)
stemmermanniae
Lycopodiaceae
Wawae1iole
U.S.A. (HI)
C*
3
R1
Microlepia strigosa var.
mauiensis (= Microlepia
mauiensis)
Dennstaedtiaceae
Palapalai
U.S.A. (HI)
C
3
R4
Trichomanes punctatum
floridanum
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
Lead
region
Historical range
Scientific
name
Family
Common name
Code
Expl.
SNAILS
Rc
A
R6
Stagnicola bonnevillensis
Lymnaeidae
Pondsnail, fat-whorled
(=Bonneville)
U.S.A. (UT)
Shrimp, troglobitic
groundwater
U.S.A. (PR),
Barbuda, Dominican Republic
CRUSTACEANS
Rc
A
R4
Typhlatya monae
Atyidae
FLOWERING PLANTS
Rc
A
R4
Calliandra locoensis
Mimosaceae
No common name
U.S.A. (PR)
Rc
A
R4
Calyptranthes estremerae
Myrtaceae
No common name
U.S.A. (PR)
E
L
R1
Phyllostegia hispida
Lamiaceae
No Common Name
U.S.A. (HI)
jlentini on DSKJ8SOYB1PROD with PROPOSALS3
[FR Doc. E9–26841 Filed 11–6–09; 8:45 am]
BILLING CODE 4310–55–S
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Agencies
[Federal Register Volume 74, Number 215 (Monday, November 9, 2009)]
[Proposed Rules]
[Pages 57804-57878]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E9-26841]
[[Page 57803]]
-----------------------------------------------------------------------
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. 74, No. 215 / Monday, November 9, 2009 /
Proposed Rules
[[Page 57804]]
-----------------------------------------------------------------------
DEPARTMENT OF THE INTERIOR
Fish and Wildlife Service
50 CFR Part 17
[Docket No. FWS-R9-ES-2009-0075; 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 remove species
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 eight candidates, and removes four 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 249.
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, 2008,
through September 30, 2009.
We request additional status information that may be available for
the 249 candidate species identified in this CNOR.
DATES: We will accept information on this Candidate Notice of Review at
any time.
ADDRESSES: This notice is available on the Internet at https://www.regulations.gov, and https://endangered.fws.gov/candidates/. 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 Internet website (https://endangered.fws.gov/candidates/). 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 in preparing listing
documents and future revisions to the notice of review, as it will help
us in monitoring changes in the status of candidate species and in
management for conserving them. 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 in 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. A species may be indentified by us as a
candidate for listing based on an evaluation of its status that we
conducted on our own initiative, or as a result of making a finding on
a petition to list a species 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 require protection under
the Act or additional species that may require the Act's protections;
and to request
[[Page 57805]]
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 in
SUPPLEMENTARY INFORMATION or visit our Internet website, https://endangered.fws.gov/candidates/.
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
December 10, 2008 (73 FR 75176). CNORs published since 1994 are
available on our Internet website, https://www.fws.gov/endangered/candidates/. 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). Guidelines for such a
priority-ranking guidance system is required under section 4(h)(3) of
the Act (15 U.S.C. 1533(h)(3)). 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. When
evaluating the magnitude of the threat(s) facing the species, we
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; and whether the effects are
likely to be permanent.
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. 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 guidance is available on our website at: https://www.fws.gov/endangered/policy/. 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 imminence 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 CNOR on December 10, 2008 (73 FR 75176),
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 eight candidates (see
Listing Priority Changes in Candidates, below) and determine that
listing proposals are not warranted for four species and thus remove
them from candidate status (see Candidate Removals, below). Combined
with the other decisions published separately from this CNOR for
individual species that previously were candidates, a total of 249
species (including 110 plant and 139 animal species) are now candidates
awaiting preparation of rules proposing their listing. These 249
species, along with the 56 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 five
species identified in the previous CNOR as either proposed for listing
or classified as candidates that are no longer in those categories.
This includes one species for which we published a final rule to list,
plus the four species that we have determined do not warrant
preparation of a rule to propose listing and therefore have been
removed from candidate status in this CNOR.
[[Page 57806]]
New Candidates
Below we present a brief summary of one new mammal, one new fish,
one new mussel, 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
Internet website (https://endangered.fws.gov/candidates/). 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 three
other species, yellow-billed loon, roundtail chub (Lower Colorado River
Basin population), and Astragalus anserinus (Goose Creek milkvetch)
were identified as candidates earlier this year as a result of a
separate petition findings published in the Federal Register.
Mammals
Florida bonneted bat (Eumops floridanus) - The following summary is
based on information in our files. Endemic to south Florida, this
species is known to occur at 12 locations, 5 on private land and 7 on
public land. The entire population may number less than a few hundred
individuals. Recent 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).
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 because the
locations of any such sites are unknown. 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, distance between occupied locations, and small number of
occupied locations. Such factors may make recolonization unlikely if
any site is extirpated and 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 and insect abundance, and disruption
of the maternal period. 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.
Birds
Yellow-billed loon (Gavia adamsii) - We previously announced
candidate status for this species in a separate warranted-but-precluded
12-month petition finding published on March 25, 2009 (74 FR 12931).
Also, see summary below under ``Petition Findings.''
Fishes
Roundtail chub (Lower Colorado River Basin DPS) (Gila robusta) - We
previously announced candidate status for this species in a separate
warranted- but-precluded 12-month petition finding published on July 7,
2009 (74 FR 32351).
Diamond darter (Crystallaria cincotta) - The following summary is
based on information contained in our files. The diamond darter is a
member of the Perch family (Percidae) that is generally translucent
with silvery white on the ventral side of the body and head and has
four wide olive-brown saddles on the back and upper side. The fish
generally grows to between 73 to 77.3 millimeters (2.9 - 3.0 inches) in
standard length. The species is a benthic invertivore (feeds on
invertebrates) that inhabits moderate to large warm-water streams with
moderate current and clean sand and gravel substrates.
Historical records indicate that the diamond darter was distributed
throughout the Ohio River Basin and that the range included the
Muskingum River, Ohio; the Ohio River, Ohio; the Green River, Kentucky;
and the Cumberland River Drainage, Kentucky and Tennessee. The species
is currently only known to exist within a 36-kilometer (km) (22.4-mile
(mi)) section of the lower Elk River in Kanawha and Clay Counties, West
Virginia, and is considered extirpated from the remainder of the Ohio
River Basin. Survey results and independent publications indicate that
the diamond darter is very rare and that the remaining population
within the Elk River is likely very small. Despite repeated and
targeted survey efforts within the species' known range and preferred
habitat in the Elk River, only 18 individuals have been collected in
the last 29 years.
The primary threats to the diamond darter are related to the
present or threatened destruction, modification, or curtailment of its
habitat or range. The Elk River Watershed is threatened with ongoing
water-quality degradation and habitat loss from activities such as coal
mining, oil and gas development, siltation from these and other
sources, and inadequate sewage and wastewater treatment. The
impoundment of rivers in the Ohio River Basin, such as the Kanawha,
Ohio, and Cumberland, has eliminated much of the species' habitat and
isolated the existing population from other watersheds that the species
historically occupied. Invasive species have the potential to affect
the Elk River and diamond darter habitat. The small size and restricted
range of the remaining diamond darter population make it particularly
susceptible to the effects of genetic inbreeding, as well as potential
extirpation from spills and other catastrophic events. The species is
vulnerable to overutilization for scientific purposes; however, the
significance of this threat has been reduced and can be further
minimized through the administration of existing scientific collecting
permit procedures. Existing Federal and State regulatory mechanisms do
not currently provide protections for the species or its habitat.
[[Page 57807]]
The threats to the diamond darter are high in magnitude, in that
the entire current range of the species is potentially affected, and
the effects of the threats severely affect the reproductive capacity
and can result in total mortality. The threats to the species are
imminent and ongoing. Activities that pose a threat to the species
already exist within the watershed and are expected to continue. Based
on imminent threats of a high magnitude, we assigned an LPN of 2 to
this species.
Clams
Rabbitsfoot (Quadrula cylindrica cylindrical) - The following
summary is based on information in our files. The rabbitsfoot is a
freshwater mussel native to Alabama, Arkansas, Georgia, Illinois,
Indiana, Kansas, Kentucky, Louisiana, Mississippi, Missouri, Ohio,
Oklahoma, Pennsylvania, Tennessee, and West Virginia. The species has
disappeared from 5 of 6 rivers in the Lower Great Lakes sub-basin, 47
of 64 rivers in the Ohio River system, 10 of 12 rivers in the
Cumberland River basin, 14 of 19 rivers in the Tennessee River system,
2 of 5 rivers in the Lower Mississippi River sub-basin, 3 of 12 rivers
in the White River system, 4 of 8 rivers in the Arkansas River system,
and 4 of 11 rivers in the Red River system, representing approximately
a 65-percent decline of its range. Total range reduction (river miles)
and overall population loss for the rabbitsfoot may approach, if not
exceed, 90 percent. Of the 49 extant populations, 10 populations are
considered to be viable in the longterm.
Population declines continue in most of the species' range, and
numerous threats, including water-quality degradation, loss of stable
substrates, sedimentation, channelization, gravel mining, dredging, and
impoundments, are affecting the few remaining sustainable extant
populations. The small size of most of the remaining rabbitsfoot
populations exacerbates the threats and adverse effects of chance
events to rabbitsfoot.
Threats to the continued existence of rabbitsfoot include exotic
species, especially zebra mussels; delivery and deposition of fine
sediments; small population sizes; isolation of populations; livestock
grazing; wastewater effluents; mine runoff; unstable and coldwater
flows downstream of dams; gravel mining; and channel dredging. In
addition, the rabbitsfoot, like many other fresh-water mussels,
requires a fish host to transport it larvae, and the fish host of
rabbitsfoot is unknown for the eastern portion of its range; thus,
artificial propagation of the rabbitsfoot to reestablish the species in
restored habitats and to maintain non-reproducing populations is not
possible, nor is focused conservation of its fish host. Although there
are ongoing attempts to alleviate some of these threats at some
locations, there appear to be no populations without significant
threats and many threats are without obvious or readily available
solutions. The threats described above have led to the species being
intrinsically vulnerable to extirpation.
Due to the number of extant populations and relatively broad
distribution, the threats to rabbitsfoot are of moderate magnitude.
Although some of the threats are nonimminent, most are ongoing and,
therefore, overall, the threats are imminent. Thus, we assigned an LPN
of 9 to this subspecies.
Flowering Plants
Astragalus anserinus (Goose Creek milkvetch) - We previously
announced candidate status for this species in a separate warranted-
but-precluded 12-month petition finding published on September 10, 2009
(74 FR 46521).
Leavenworthia exigua var. laciniata (Kentucky gladecress) - The
following summary is based on information in our files. Kentucky
gladecress is a winter annual that is adapted to environments with
shallow soils interspersed with flat-bedded limestones. The natural
habitat for Kentucky gladecress is cedar glades, but the variety is
also known from overgrazed pastures, eroded shallow-soil areas with
exposed bedrock, and areas where the soil has been scraped off the
underlying bedrock. The variety does not appear to compete well with
other vegetation and is shade intolerant. Currently, there are
approximately 55 occurrences in Jefferson and Bullitt Counties,
Kentucky, but at least 39 of these occurrences are of poor quality with
low numbers of plants and degraded conditions.
Populations of this variety are now located primarily in modified
habitats such as pastureland, roadside rights of way, and cultivated or
plowed fields. These populations are threatened by further habitat
destruction (conversion from rural to residential land use), herbicide
use, overgrazing, and competition. Some populations continue to occupy
natural glade habitats, but these habitats are remnant in nature and
continue to be affected by agricultural and residential conversion. The
variety's primary threat, habitat destruction due to residential and
commercial development, is widespread and has the potential to affect
the entire range of the variety. The effects of the threat are also
permanent. Therefore, these threats are high in magnitude. These
threats are imminent because the conversion from rural to residential
land use is ongoing. Consequently, we assigned an LPN of 3 to this
plant variety.
Ferns and Allies
Trichomanes punctatum ssp. floridanum (Florida bristle fern) - The
following summary is based on information in our files. The Florida
bristle fern has been reduced to four, or possibly five, small,
isolated occurrences: Three occur in Miami-Dade County and two in
Sumter County. In Miami-Dade County, it has been found exclusively in
solution holes in oolitic limestone and rocky outcrops in rockland
hammocks. In Sumter County, plants occur in a mesic/hydric hammock on
shaded limestone boulders.
Most sites where Florida bristle fern once occurred in Miami-Dade
County have been lost; few rockland hammocks remains outside of
Everglades National Park. Impacts from regional water drainage in
Miami-Dade County are severe, and currently occurring. Regional
drainage in remaining habitat has probably been a stressor that has
contributed to extirpations and population declines. Resulting drops in
ambient humidity in the habitat may limit reproduction and health of
populations over the longterm. Such changes in humidity may cause
extirpations or make plants more vulnerable to other stressors (e.g.,
periodic long-term droughts, hurricanes). Climatic changes and sea-
level rise are future, long term threats that are expected to affect
habitat and ultimately reduce the extent of available habitat in Miami-
Dade County. Agricultural conversion and development are currently
occurring in Sumter County, placing any undocumented occurrences and
suitable habitat at risk. Since a full survey of suitable habitats for
the Florida bristle fern has never been conducted in Sumter County, we
cannot determine the full extent of losses of this species due to
habitat destruction and modification. All known extant occurrences are
located on conservation lands; however, there is potential, especially
in Sumter County, for the species to occur on private lands. Together,
the extant occurrences contain fewer than 1,000 plants. Many plants are
probably clones, so there may be limited genetic diversity within
sites. Because there are few occurrences, populations contain few
plants, and
[[Page 57808]]
genetic variability is low, the species is inherently at risk due to
stochastic events. Droughts, tropical storms, and hurricanes are
threats; Hurricane Andrew may have played a role in the extirpation of
the species from two sites. Since there are few occurrences remaining,
the species is threatened with extinction during these events. Invasive
exotic plants are also a threat, but may be reduced due to active
programs by Miami-Dade County and the State. The extent to which fungus
is a threat to wild populations is unknown. Overall, the magnitude of
threats is high, and most threats are occurring and are, therefore,
imminent. Consequently, we assigned this subspecies an LPN of 3.
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 imminence 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.
Birds
Elfin-woods warbler (Dendroica angelae) - The 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 of Puerto Rico,
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,
Sierra de Cayey, and the Commonwealth forests of Maricao and Toro
Negro. However, it has not been recorded again in Toro Negro and Cayey
since 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 Forest, Guilarte Forest, Bosque del Pueblo, Maricao
Forest and the El Yunque National Forest (Luquillo Mountains), but the
species was detected only in the latter two. In the Maricao
Commonwealth Forest, 778 elfin-woods warblers were recorded, and in the
El Yunque National Forest, 196 were recorded.
The elfin-woods warbler is threatened by habitat modification.
Destruction of elfin forest and Podocarpus forest by the installation
of infrastructure (telecommunication towers and 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 Department of Natural
and Environmental Resources potentially installing these structures.
Furthermore, restoration of this habitat would take a few 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 shade-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 sun-coffee plantations) may result in ineffective
corridors for dispersal and expansion of the elfin-woods warbler.
Although 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. We previously assessed the LPN
as a 5 (high magnitude, nonimminent threats). 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 the species 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, we
have determined that the magnitude of threats is moderate to low
because the severity of the threats on the species is not as great as
we previously believed and most of the range of the elfin-woods warbler
is within protected lands. The threats are not currently occurring in
most of the warbler's habitat; therefore, the threats are nonimminent.
As a result, we have changed the LPN from a 5 to an 11 for this
species.
Fish
Pearl darter (Percina aurora) - Little is known about the specific
habitat requirements or natural history of the Pearl darter. Pearl
darters have been collected from rivers and streams with a variety of
attributes, but are mainly found 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 non-point 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 reductions casused by 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 and would
also make this species more vulnerable to catastrophic events.
Reevaluation of the threats affecting the pearl darter has indicated
that a change in the Listing Priority Number is warranted. Threats
affecting the pearl darter are localized in nature, affecting portions
of the population within the drainage. Thus, a threat magnitude of
moderate to low is a more appropriate category in this situation. In
addition, since the identified threats are currently affecting this
species in these portions of its range, the threats are imminent.
Therefore, we have changed the LPN from a 5 to an 8 to reflect this
reevaluation.
Clams
Neosho mucket (Lampsilis rafinesqueana) - 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) of its range, primarily 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 historical range have been inundated by
the
[[Page 57809]]
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 to
this river. The rapid collapse of the entire mussel community,
including Neosho mucket, since 2005 in the Arkansas portion of the
Illinois River threatens to extirpate the species from approximately 30
river miles 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 because of their severity on this
species, and they occur throughout the range. The majority of the
threats are ongoing and thus imminent. Thus, we changed the LPN from a
5 to a 2 for this species.
Insects
Miami blue butterfly (Cyclargus thomasi bethunebakeri) - The Miami
blue is endemic to south Florida. Historically, it occurred throughout
the Florida Keys, 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, and along trails and other open sunny areas, and
historically in pine rocklands. These habitats provide host plants 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 hostplants from iguanas
at BHSP is a new, ongoing, significant threat; although active steps
are being taken by the State, 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, mosquito control, and accidental harm from humans;
increasing the current population in size; and establishing populations
at other locations. The threats are high in magnitude and constitute a
significant risk to the subspecies. Given that the new threat from
iguanas and other threats (hurricanes, few occurrences, and small
population size) are ongoing, the threats are imminent. Therefore, we
changed the LPN from a 6 to a 3.
Flowering plants
Helianthus verticillatus (whorled sunflower) - 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 area; 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 habitat, the other Alabama
population has responded favorably to canopy removal that took place
circa 2001. Because of this, the threats are of moderate magnitude. The
threats are currently occurring, and therefore imminent. To help ensure
consistency in the application of our listing priority process, we
changed the LPN from a 5 to an 8 for this species.
Lesquerella globosa (Short's bladderpod) - 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; 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 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 many locations, active habitat management is
necessary at those sites. The threats from roadside maintenance and
habitat alterations by invasive plant encroachment are moderate in
magnitude, as they are not affecting all locations of this species.
However, the threats are currently occurring, and therefore imminent.
To help ensure consistency in the application of our listing priority
process, we changed the LPN from a 5 to an 8 for this species.
Physaria douglasii ssp. tuplashensis (White Bluffs bladderpod) - In
previous Candidate Notices of Review, we referred to P. douglasii ssp.
tuplashensis as P. tuplashensis. We have now dropped that name because
the paper that recommended its use was never published. As a result, we
are following
[[Page 57810]]
the treatment of a 2002 published scientific paper that recognized the
White Bluffs bladderpod as Physaria douglassii ssp. tuplashensis.
White Bluffs bladderpod is a low-growing, herbaceous, short-lived
perennial plant in the Brassicaceae (mustard) family. Historically and
currently, White Bluffs bladderpod (P. douglasii ssp. tuplashensis) has
been known from only 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 33 feet (10
meters) wide by 10.6 miles (17 km) 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. However, the southern
portion 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 destroy plants, and the presence
of invasive nonnative plants that compete with P. douglassii ssp.
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 ssp.
tuplashensis population. As a result of a fire in 2007, there is a
higher probability that invasion of these nonnatives will occur. We
reanalyzed the magnitude and imminence of the threats, which resulted
in a change in the LPN for P. douglasii ssp. tuplashensis. 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 and 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 relatively 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 85 percent having Federal ownership.
Even though off-road vehicle use is prohibited on the monument,
intermittent, ongoing use does occur. However, these activities,
although they are ongoing, are mainly confined to the upper portion of
the White Bluffs where few P. 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 described as
a significant problem. While P. douglasii ssp. tuplashensis is
inherently vulnerable because it is a narrow endemic, the magnitude of
the threats to the population is moderate. The threats are currently
occurring, and therefore imminent. To help ensure consistency in the
application of our listing priority process and to recognize the
correct taxonomic name, we changed the LPN from a 5 to a 9 for this
subspecies.
Platanthera integrilabia (White fringeless orchid) - Platanthera
integrilabia is a perennial herb that grows in partially but not fully
shaded, wet, boggy areas at the heads of streams and on seepage slopes
in Alabama, Georgia, Kentucky, and Tennessee. Historically, there were
at least 90 populations of P. integrilabia. Currently there are
approximately 50 extant sites supporting the species.
Several populations have been extirpated due to road, residential,
and commercial construction and 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. All-terrain 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 that the hydrology of the bogs that support the
species is not altered. Natural succession can result in decreased
light levels. Because of the species' dependence upon moderate to high
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 by 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 threaten several sites. Upon review of current
listing guidance and threats affecting the species, we have revised the
LPN to reflect the fact that threats are currently operating at most
sites and are therefore imminent. While 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 the threats by being within State parks, national forests,
wildlife management areas, or other protected land. As a result, we
changed the LPN from a 5 to an 8 for this species.
Candidate Removals
As summarized below, we have evaluated the threats to the following
four species and considered factors that, individually and in
combination, currently or potentially could pose a risk to these
species and their habitat. After a review of the best available
scientific and commercial data, we conclude that listing these four
species under the Endangered Species Act is not warranted because the
species are not likely to become endangered species within the
foreseeable future throughout all or a significant portion of their
range. Therefore, for each of these species 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 these species, and to accept additional information and comments
concerning this finding. We will reconsider our determination for each
species in the event that new information indicates that the threats to
the species are of a considerably greater magnitude or imminence than
identified through assessments of information contained in our files,
as summarized here.
Snails
Fat-whorled pondsnail (Stagnicola bonnevillenis) - The fat-whorled
pondsnail, also known as the Bonneville pondsnail, was thought to occur
in only four spring pools north of the Great Salt Lake in Box Elder
County, Utah. Additional surveys found Lymnaeid snails including S.
bonnevillensis-like
[[Page 57811]]
shells in springs throughout the playa. New information shows that
shell characteristics vary greatly with environmental conditions.
Because the fat-whorled pondsnail was classified based only on the
shell appearance, the taxonomy is questionable. Because of
uncertainties surrounding the validity of S. bonnevillensis as a
species, we evaluated all Stagnicola sp. inhabiting the spring pools
previously thought to be occupied by S. bonnevillensis. The primary
threat to these pools has been chemical contamination of the
groundwater. Significant actions have been taken to remediate this
threat, including implementing corrective actions to track and
remediate groundwater contamination, implementation of a site
management plan, and development of a groundwater model and risk
assessment. The plan has been implemented, and conservation measures
are currently being monitored for effectiveness. These efforts have
been under way for a sufficient period to effectively eliminate the
threat from contamination. We know of no other threats to the springs
in the range of S. bonnevillensis. Based on findings and analysis in
our updated assessment, we conclude that this species in not likely to
become an endangered species within the foreseeable future throughout
all or a significant portion of its range, and listing this species
under the Endangered Species Act is therefore not warranted. The
species no longer meets our definition of a candidate, and we have
removed it from candidate status.
Crustaceans
Troglobitic groundwater shrimp (Typhlatya monae) - Typhlatya monae
is a small subterranean small shrimp known from Puerto Rico, Barbuda,
and the Dominican Republic. It is classified as a troglobite, or
obligatory cave organism, of which its most extraordinary feature is
the reduction or loss of vision and pigmentation. T. monae feeds on
organic waste material and debris, such as bat guano. Little is known
concerning the status of T. monae in either Barbuda or Dominican
Republic and we are not aware of any threats to this species in those
locations. This species was discovered on Mona Island, in Puerto Rico
but was later found on the Puerto Rico mainland in three caves within
the Gu[aacute]nica Commonwealth Forest in the municipalities of
Gu[aacute]nica, Yauco, and Guayanilla. Although the species was not
found on Mona Island during surveys conducted in 1974 and 1995, the
species may still be found in the reef deposit aquifers in Mona Island
that have not yet been surveyed.
In 1995, the total population was estimated to be close to 2,000
individuals; over 95 percent of these were observed in one cave.
Although no systematic censuses have been conducted since 1995, the
Service has recently documented the presence of the species in all
three mainland caves and obtained information from Puerto Rico
Commonwealth Forest personnel regarding two additional caves in which
the species may occur.
In past reviews, we determined that the species was threatened by
habitat disturbance, human-induced fires, hurricanes and floods.
However, the Gu[aacute]nica Commonwealth Forest and Mona Island Natural
Reserve are managed for conservation by the Puerto Rico Department of
Natural and Environmental Resources (DNER). Caves in the Gu[aacute]nica
Forest are closed to public visitors; therefore, habitat modification
and disturbance, and human-induced fires are not anticipated. Caves on
Mona Island are seldom visited, and adverse effects to these areas have
not been documented. The species is located in pools inside caves, and
underground waters; thus, we do not anticipate impacts from hurricanes.
Typhlatya monae was first described in Mona Island from el Pozo Del
Portuguez and from a deep well close to the airport. At the present
time, the use of this well is limited to DNER staff; therefore,
additional extraction of underground waters is not expected. Currently,
the DNER utilizes water cisterns and commercial potable water as
alternate water sources. The species is protected by Regulation
6766 (``Reglamento para Regir las Especies Vulnerables y en
Peligro de Extinci[ouml]n en el Estado Libre Asociado de Puerto
Rico''), adopted in 2004 by the Commonwealth of Puerto Rico. Under
Regulation 6766, T. monae is listed as Critically Endangered
(CR). Regulation 6766 prohibits collecting, killing, or
harming listed species. We conclude that this species in not likely to
become an endangered species within the foreseeable future throughout
all or a significant portion of its range, and listing this species
under the Endangered Species Act is not warranted. The species no
longer meets our definition of a candidate, and we have removed it from
candidate status.
Flowering Plants
Calliandra locoensis (no common name) - Calliandra locoensis is a
spiny, leguminous shrub currently known from five localities within the
Susu[aacute] Commonwealth Forest in the municipalities of Yauco and
Sabana Grande, in southwestern Puerto Rico. This species is endemic to
Puerto Rico, and was discovered in 1991 during a study of the flora of
the Susu[aacute] Commonwealth Forest; it was described by Garci[aacute]
and Kolterman in 1992. Calliandra locoensis is found on shallow,
serpentine soils with low nutrients, high drainage, and low fertility.
In 2007, local botanists reported 3 populations with approximately
1,600 adult plants and numerous seedlings in 5 localities indicating
that the number of adult individuals has doubled and the number of
localities has increased since surveys conducted in 1998.
In previous reviews, we determined that the species was threatened
by forest-management practices (accidental trampling, brush clearing,
trail maintenance), forest fires (natural or manmade), catastrophic
natural events (hurricanes, floods, mudslides), and restricted
distribution. We now find that this species is not currently threatened
by forest management practices. The species is currently considered as
a critical element under the Puerto Rico Department of Natural and
Environmental Resources Natural Heritage Program; consequently
activities conducted in the forest are generally scrutinized and
measures to minimize or avoid impacts to species are recommended and
implemented. The Susu[aacute] Commonwealth Forest is also protected by
Law 133 and has been designated as a Critical Wildlife Area.
We also previously indicated that this species was vulnerable to
hurricanes and human-induced fires. Plants endemic to the Caribbean are
naturally adapted to the impact of hurricanes (the species usually lose
their leaves for a certain period of time, but recover them later).
Although hurricanes are common occurrences in Puerto Rico, damage to
this species by hurricanes has not been reported in any of the
currently known populations in the last decade. Surveys have indicated
that despite hurricanes occurring in the areas where C. locoensis
exists, the number of adult individuals has doubled, the number of
localities has increased, evidence suggests that the species is
successfully reproducing. Thus, we have determined that hurricanes are
not a threat. The currently known populations are not located near the
roads of the forest, which are more vulnerable to fires and DNER
implements a fire prevention plan within the forest, particularly
during the dry season; therefore, fire is not a threat to the species.
We conclude that this species in not likely to become
[[Page 57812]]
an endangered species within the foreseeable future throughout all or a
significant portion of its range, and listing this species under the
Endangered Species Act is not warranted. The species no longer meets
our definition of a candidate, and we have removed it from candidate
status.
Calyptranthes estremerae (no common name) - Calyptranthes
estremerae is a small tree from the subtropical moist forest of
northwestern Puerto Rico, in the municipalities of Camuy, Utuado, and
Arecibo. Calyptranthes estremerae was only known from several
individuals found near the recreation area adjacent to the Rio Camuy
Cave Park. At present time, about 100 individuals of C. estremerae are
estimated for the Camuy Cave Park area, Rio Abajo Commonwealth Forest
(managed by the Puerto Rico Department of Natural and Environmental
Resources (DNER)), and a privately owned farm in Sabana Hoyos, Arecibo.
We have found that this species is no longer threatened by the
expansion of recreation facilities within Cavernas de Camuy Park and
Rio Abajo Commonwealth Forest, as there are no plans to expand such
facilities. In addition, the Rio Abajo Commonwealth Forest has a
management plan in place that emphasizes protection and conservation of
species classified under DNER as critical, threatened, or endangered
and their habitat; C. estremerae is classified as a critical element by
DNER. Furthermore, actions that may affect such classified species are
generally scrutinized, and measures to minimize or avoid impacts to
these species are recommended and implemented. The Rio Abajo
Commonwealth Forest is also protected by designation as a Critical
Wildlife Area. In previous assessments, we indicated that the small
number of individuals of C. estremerae in the two populations, along
with the species' limited distribution made this species vulnerable to
potential catastrophic natural (hurricanes) and manmade (fires) events.
However, damage by hurricanes has not been reported in any of the
currently known populations. In addition, because the species exists in
the subtropical moist forest life zone, the threat of human-induced
fires is low; further, the DNER implements an islandwide fire
prevention plan in public forests. Therefore, fires are currently not a
threat to this species. We conclude that this species in not likely to
become an endangered species within the foreseeable future throughout
all or a significant portion of its range, and listing this species
under the Endangered Species Act is not warranted. The species 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. Under section 4(b)(3)(A),
when we receive such a petition, we must determine within 90 days, to
the maximum extent practicable, whether the petition presents
substantial information 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