Endangered and Threatened Wildlife and Plants; Review of Native Species That Are Candidates or Proposed for Listing as Endangered or Threatened; Annual Notice of Findings on Resubmitted Petitions; Annual Description of Progress on Listing Actions, 24870-24934 [05-9283]
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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 or Proposed for
Listing as Endangered or Threatened;
Annual Notice of Findings on
Resubmitted Petitions; Annual
Description of Progress on Listing
Actions
Fish and Wildlife Service,
Interior.
ACTION: Notice of review.
AGENCY:
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 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 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 to each species.
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.
We request additional status
information that may be available for
the 286 candidate species. 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 that
we should include as candidates as we
prepare future updates of this list.
This document also includes our
findings on resubmitted petitions and
describes our progress in revising the
Lists of Endangered and Threatened
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Wildlife and Plants during the period
May 5, 2004, through May 2, 2005.
DATES: We will accept comments on the
Candidate Notice of Review at any time.
ADDRESSES: Submit your comments
regarding a particular species to the
Regional Director of the Region
identified in SUPPLEMENTARY
INFORMATION as having the lead
responsibility for that species. You may
submit comments of a more general
nature to the Chief, Division of
Conservation and Classification, U.S.
Fish and Wildlife Service, 4401 N.
Fairfax Drive, Room 420, Arlington, VA
22203 (703/358–2171). Written
comments and materials received in
response to this notice will be available
for public inspection by appointment at
the Division of Conservation and
Classification (for comments of a general
nature only) or at the appropriate
Regional Office listed in SUPPLEMENTARY
INFORMATION.
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 Division of Conservation and
Classification, Arlington, Virginia (see
address above), or on our Internet Web
site (https://endangered.fws.gov/
candidates/).
FOR FURTHER INFORMATION CONTACT: The
Endangered Species Coordinator(s) in
the appropriate Regional Office(s) or
Chris Nolin, Chief, Division of
Conservation and Classification (703–
358–2171).
SUPPLEMENTARY INFORMATION:
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. Through the Federal
rulemaking process, we add these
species 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
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actions. We maintain this list 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
conservation efforts that will remove or
reduce threats to these species; to solicit
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
solicit necessary information for setting
priorities for preparing listing proposals.
Table 1 includes 286 species that we
regard as candidates for addition to the
Lists of Endangered and Threatened
Wildlife and Plants (Lists), as well as 21
species for which we have published
proposed rules to list as threatened or
endangered species. Most of these
proposed species were previously
identified in the 2003 CNOR (69 FR
24876, May 4, 2004). We encourage
consideration of these species in
conservation planning, as well as other
environmental planning, such as in
environmental impact analysis done
under the National Environmental
Policy Act of 1969 (implemented at 40
CFR parts 1500–1508) and in local and
statewide land use planning. Table 2
contains eight species we identified as
candidates or as proposed species in the
May 4, 2004, CNOR that we now no
longer consider candidates. This
includes two species that we listed as
threatened since May 4, 2004, one
species that we withdrew the proposed
rule, one species that we removed from
candidacy through a notice published
on August 18, 2004 (69 FR 51217), and
four species that we are removing from
candidacy through this notice. The
Region having lead responsibility for the
particular species maintains updated
records of information on candidate
species.
Previous Notices of Review
The Act directed the Secretary of the
Smithsonian Institution to prepare a
report on endangered and threatened
plant species, which was published as
House Document No. 94–51. We
published a notice in the Federal
Register on July 1, 1975 (40 FR 27823),
in which we announced that we would
review more than 3,000 native plant
species named in the Smithsonian’s
report and other species added by the
1975 notice for possible addition to the
List of Endangered and Threatened
Plants. A new comprehensive notice of
review for native plants, which took
into account the earlier Smithsonian
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report and other accumulated
information, superseded the 1975 notice
on December 15, 1980 (45 FR 82479).
On November 28, 1983 (48 FR 53640),
a supplemental plant notice of review
announced changes in the status of
various species. We published complete
updates of the plant notice on
September 27, 1985 (50 FR 39526);
February 21, 1990 (55 FR 6184);
September 30, 1993 (58 FR 51144); and,
as part of combined animal and plant
notices, on February 28, 1996 (61 FR
7596); September 19, 1997 (62 FR
49398); October 25, 1999 (64 FR 57534);
October 30, 2001 (66 FR 54808); June
13, 2002 (67 FR 40657); and May 4,
2004 (69 FR 24876). Additionally, on
January 8, 2001 (66 FR 1295), we
published our resubmitted petition
finding for one plant species having an
outstanding ‘‘warranted-but-precluded
finding’’ on a petition to list.
We published earlier comprehensive
reviews for vertebrate animals in the
Federal Register on December 30, 1982
(47 FR 58454), and on September 18,
1985 (50 FR 37958). We published an
initial comprehensive review for
invertebrate animals on May 22, 1984
(49 FR 21664). We published a
combined animal notice of review on
January 6, 1989 (54 FR 554), and with
minor corrections on August 10, 1989
(54 FR 32833). We again published
comprehensive animal notices on
November 21, 1991 (56 FR 58804);
November 15, 1994 (59 FR 58982); and,
as part of combined animal and plant
notices, on February 28, 1996 (61 FR
7596); September 19, 1997 (62 FR
49398); October 25, 1999 (64 FR 57534);
October 30, 2001 (66 FR 54808); June
13, 2002 (67 FR 40657); and May 4,
2004 (69 FR 24876). Additionally, on
January 8, 2001 (66 FR 1295), we
published our resubmitted petition
findings for 25 animal species having
outstanding ‘‘warranted-but-precluded’’
petition findings as well as notice of one
candidate removal.
This revised notice supersedes all
previous animal, plant, and combined
notices of review.
Summary
Since publication of the 2003 CNOR
on May 4, 2004 (69 FR 24876), we
reviewed the available information on
candidate species to ensure that a
proposed listing is justified for each
species and reevaluated the relative
listing priority assignment of each
species. A candidate species is assigned
a listing priority number (LPN) of 1–12
depending on the magnitude of threats,
the imminence of threats, and by its
taxonomic status in accordance with our
priority guidance as published on
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September 21, 1983 (48 FR 43098). We
also evaluated the need to emergencylist any of these species, particularly
species with high priorities (i.e., species
with listing priority numbers of 1, 2, or
3). This review and reevaluation ensures
that we focus conservation efforts on
those species at greatest risk. As of May
2, 2005, 18 animals are proposed for
endangered status; 2 animals are
proposed for threatened status (not
including proposed reclassifications of
endangered species); 1 animal is
proposed for threatened-due-tosimilarity-of-appearance status; and 145
plant and 141 animal candidates are
awaiting preparation of proposed rules
(see Table 1). Table 2 includes eight
species we previously classified as
either proposed for listing or candidates
that we no longer classify in those
categories.
Summary of New Candidates
Below we present brief summaries of
five new candidates, including one
species of fish, one insect, one
crustacean, and two plants. 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 Web site (https://
endangered.fws.gov/candidates/
index.html).
Fish
Sicklefin redhorse (Moxostoma sp.)—
The sicklefin redhorse is a mediumsized redhorse fish, reaching up to about
18 inches, with an elongate, somewhat
compressed body and a highly falcate
(sickle-shaped) dorsal fin and are found
in North Carolina, Tennessee and
Georgia. Detailed morphological and
genetic studies have concluded that the
sicklefin redhorse is a distinct species.
The species is currently known to
occupy cool to warm, moderate gradient
creeks and rivers, and, during parts of
its early life stages, large reservoirs. In
streams, it is most often observed in
riffles, runs, and well-flowing pools. It
feeds and spawns in gravel, cobble, and
boulder substrates with no, or very
little, silt overlay.
Like many other redhorse species, the
sicklefin redhorse is known mainly from
flowing streams; however, also like
many other redhorse species, the
sicklefin redhorse appears to have
adapted to spending at least part of its
life in the near-shore areas of
impounded streams where prespawning age sicklefins have been
collected, mainly near the mouth of
streams that feed the reservoirs. Current
observations indicate that adults of the
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species are year-round residents of
rivers and large creeks and that young,
juveniles, and subadults occupy
primarily the lower reaches of creeks
and rivers and near-shore portions of
certain reservoirs. It is likely that after
emerging from the stream substrata,
many of the larvae and postlarvae are
carried downstream to the mouths of
streams or into reservoirs. Newly mature
fish (≥5 years of age) appear to migrate
from the reservoirs to spawn and then
remain in the streams with the other
adults.
Based on an analysis of preserved
specimens, the species is relatively long
lived, with both sexes living at least to
17 years of age; however, based on the
size of fish seen in the streams, some
individuals probably live for over 20
years. Spawning typically occurs over
cobble, with usually only a small
portion of sand and gravel, in moderate
to fast runs in open areas and pockets
formed by boulders and outcrops. The
spawning period for the sicklefin runs
from late April through mid-May.
Past and recent collection records of
the sicklefin redhorse, together with
what is known about the habitat
utilization of the species, indicate that
the sicklefin redhorse once inhabited
the majority, if not all, of the rivers and
large creeks in the Blue Ridge portion of
the Hiwassee and Little Tennessee River
systems in North Carolina, Tennessee,
and Georgia. Current estimates are that
the species has apparently been
eliminated from roughly 60 percent of
its former range. This is a conservative
estimate that: (1) Includes several miles
of the Hiwassee and Fontana Reservoirs
within the present range of the species
(although portions of these reservoirs
appear to provide survivable habitat for
juvenile sicklefins, they do not provide
foraging or spawning habitat for adults
of the species); and (2) does not include
some of the higher reaches of some of
the creeks where the sicklefin redhorse
currently occurs in their lowermost
reaches. Additionally, the Cheoah River,
Cullasaja River, Cartoogechaye Creek,
Oconaluftee River, and several other
large tributaries in the Hiwassee and
Little Tennessee River systems may also
have once been inhabited by the
sicklefin redhorse.
Impacts associated with the
construction and operation of dams for
hydropower generation on the streams
inhabited by the species is the primary
cause of the extirpation of the sicklefin
redhorse throughout the majority of its
former range. These impoundments
created by the dams eliminate spawning
and foraging habitat of the adult
sicklefin redhorse by changing the
conditions from flowing to still water.
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Water depth increases, flow decreases,
and silt accumulates on the bottom.
Impoundments not only destroy riverine
habitat within the impounded portion of
the stream, but they alter the quality and
stability of the downstream reaches by
adversely affecting water flow regimes,
velocities, temperature, chemistry, and
nutrient cycles. Dams that operate by
releasing cold water from near the
bottom of the reservoirs lower the water
temperature downstream, changing
downstream reaches from warm-or coolwater streams to cold-water streams and
affecting their suitability for many of the
native species historically inhabiting
these stream reaches. The effects of
impoundments result in changes in fish
and macroinvertebrate communities
(macroinvertebrates are the main prey
items of the sicklefin), species requiring
clean gravel and sand substrates are lost.
In addition, dams result in the
fragmentation and isolation of
populations of remaining populations of
the sicklefin redhorse, acting as effective
barriers to the natural upstream and
downstream expansion or recruitment
of the species. Natural upstream and
downstream population expansion and
repopulation of the majority of the
species’ former range are restricted
because of the barriers posed by the
existing dams and impacts to the
tailwaters associated with the current
operation of the dams. As a result, the
Hiwassee River system and Little
Tennessee River system populations are
isolated from each other. This isolation
decreases their ability to respond to
nature- and human-induced changes in
their environment and increases their
vulnerability to extirpation. Wastewater
discharges, together with impacts to
water and habitat quality associated
with a variety of other land disturbance
activities carried out without adequate
measures to control storm water and
erosion, also played a significant role in
the decline of the species.
Many of the same factors believed to
have contributed to the extirpation of
the species from much of its former
range potentially threaten these
remaining populations. All of the
surviving occurrences of the sicklefin
redhorse are restricted to relatively short
reaches of the streams they occupy,
primarily due to existing dams. Their
limited distributions make them
extremely vulnerable to the effects from
single catastrophic events (such as toxic
chemical spills, major sedimentation
events, channel modification, etc.) and/
or the cumulative effects of lesser
impacts to their habitat and numbers.
Although the majority of the streams
still occupied by the species occur in
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areas that are presently primarily rural,
many of the communities within the
watersheds of these streams are
experiencing increasing development
pressure, both commercial and
residential, and are developing plans for
upgrading and improving their
infrastructure (e.g., roads, water
supplies, sewer/wastewater treatment
systems, etc.) to provide for increased
densities of development.
Because of the entire current range of
the sickelefin redhorse is affected by the
threats described above, the magnitude
of the threat to the species is high.
Although the threats faced by the
sicklefin redhorse are significant, it is
not anticipated that the species will be
subject to these threats in the immediate
future. Therefore, we assigned a listing
priority of 5 to this species.
Insects
Miami blue butterfly (Cyclargus
thomasi bethunebakeri)—The Miami
blue is a coastal butterfly that occurs at
the edges of tropical hardwood
hammocks (forests) and occasionally in
tropical pinelands and along trails,
utilizing open sunny areas in southern
Florida. The geographic range of this
butterfly once extended from the Florida
Keys north along the coasts to about St.
Petersburg and Daytona, Florida.
Although little specific historic
information exists on the abundance
and distribution patterns of the Miami
blue, it is clear that the occurrence of
this butterfly throughout its historic
range has been significantly reduced,
with only small remnants remaining.
Despite extensive surveys of known
suitable habitat and/or historical
records, the species is now found only
in a single metapopulation, located at
Bahia Honda Key State Park (Park), with
a few immature individuals on West
Summerland Key. This metapopulation
is comprised of thirteen distinct
colonies in the Park.
In November 2002, the Service
worked with researchers and the State
to establish a captive propagation
program for the Miami blue due to the
low estimated population at its only
known location. As of December 2004,
the captive colony had numerous
generations, with hundreds of
individuals in captivity. Efforts have
been undertaken to reintroduce captivebred Miami blues to Federal lands (i.e.,
Everglades National Park and Biscayne
National Park) within the butterfly’s
historic range. However, subsequent
monitoring has indicated an
inconsistent or sporadic presence of
only a small number of individuals of
varying life stages at release sites.
Monitoring results do not indicate that
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the Miami blue has become established
at any of the release sites.
Extensive losses of the species’ habitat
and fragmentation of remaining patches,
along with mosquito control activities,
are the likely cause of the species’
decline. Although many areas on public
lands may offer suitable nectar and
other host plants, the extremely limited
dispersal ability of the species likely
prevents these areas from becoming
occupied and used. The Miami blue
butterfly is threatened by the combined
influences of habitat destruction and
modification, mosquito control
activities, and loss of genetic diversity
associated with isolated populations.
The possibility for catastrophic events
(e.g., hurricanes) also poses a threat to
the survival of this butterfly. In addition
to these threats, habitat loss and
fragmentation, fire suppression,
displacement of native host plants by
invasive exotic species, detrimental
land management practices, accidental
harm from humans, and inadequate
regulatory protection pose threats to the
species throughout the species historic
range. Predation, accidental harm or
habitat destruction, and illegal
collection may also pose a threat to the
Miami blue due to the small population
size at the known locations. Due to
nonimminent threats of high magnitude
as described above, we assigned a listing
priority number of 6 to this subspecies.
Crustaceans
Diminutive amphipod (Gammarus
hyalleloides)—The diminutive
amphipod is a small amphipod that is
ranked as ‘‘critically endangered
throughout its range’’ (G1) by
NatureServe and ‘‘critically endangered
throughout its range’’ (S1) by the State
of Texas. Based on surveys and genetic
analysis, this species only occurs in four
spring outflows in the Toyah Basin,
Balmorhea area of Reeves and Jeff Davis
Counties, Texas; these springs are all
within about 8 miles (13 km) of each
other within the San Solomon Spring
System. In addition to being an
important habitat for rare aquatic fauna,
this spring system is also an important
source of irrigation water for the farming
communities in the Toyah Basin. The
primary threat to the species is the loss
of surface flows due to declining
groundwater levels from drought and
pumping for agricultural production.
`
The natural cienega habitats (marshland
communities associated with perennial
springs and headwater streams) of the
Balmorhea area have been mostly
altered over time to accommodate
agricultural irrigation. Most significant
was the draining of wetland areas and
the modification of spring outlets for
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development of human use of the water
resources. Although the land
surrounding the amphibod’s current
habitat is owned and managed by The
Nature Conservancy, Bureau of
Reclamation, and Texas Parks and
Wildlife Department, the water needed
to maintain its habitat has declined due
to a reduction in spring flows, possibly
as result of private groundwater
pumping in areas beyond that are
controlled by these landowners.
Pumping of the regional aquifer system
for agricultural production of crops has
resulted in the drying of other springs
in this region, including Comanche
Springs, which was once a large surface
spring in Fort Stockton, Texas. Another
example is Phantom Lake Spring, one of
the sites of occurrence for the
amphipod, which ceased flowing in
2000; aquatic habitat is now supported
only by a pumping system. Another
threat to amphipod habitat is the
potential degradation of water quality
from point and nonpoint pollutant
sources. This pollution can occur either
directly into surface water or indirectly
through contamination of groundwater
that discharges into spring run habitats
used by the amphipod. The primary
threat for contamination comes from
herbicide and pesticide use in nearby
agricultural areas.
Although the physical condition of
the areas where this species is found has
changed dramatically over time from
human actions, at least a portion of the
native biota remain. However, three of
the four known current occurrences of
the species are in degraded habitats (the
exception is East Sandia Spring)
because the natural conditions of the
springs have been substantially
modified for human use. Any additional
modifications to the spring flow habitats
will further threaten the species.
Therefore, with imminent threats of
high magnitude, we assign this species
a listing priority number of 2.
Flowering Plants
Ipomopsis polyantha (Pagosa
skyrocket)—Pagosa skyrocket is an
extremely narrow endemic with a global
distribution limited to a 13-mile range
on outcrops of Pagosa-Winifred soils
derived from mancos shale in Archuleta
County, Colorado. The total population
size is estimated to be between 2,246
and 10,626 plants. It is ranked as
‘‘critically endangered throughout its
range’’ (G1) by NatureServe and
‘‘critically endangered in the state’’ (S1)
by the Colorado Natural Heritage
Program. Populations are on federal
highway rights of way and private
lands. Much of the occupied habitat on
private lands has been subdivided and
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is being rapidly developed. There are no
plans being implemented for the
management, protection, or
conservation of the species. The
Colorado Rare Plant Technical
Committee, including botanists from the
Colorado Natural Heritage Program, has
identified I. polyantha as the species
most in need of protection and recovery
efforts in 2005 in Colorado. We assign
this species a listing priority number 2
based on imminent habitat destruction
throughout its narrow range.
Solidago plumosa (Yadkin River
goldenrod)—A member of the
Asteraceae family, Solidago plumosa is
endemic to the Yadkin River in North
Carolina and was originally described
from the Narrows Canyon and Falls area
of this river in 1894. Currently, plants
are know to exist in only two locations,
located approximately 2 kilometers
apart along the shoreline of the Yadkin
River in North Carolina. This species is
ranked as ‘‘critically endangered
throughout its range’’ (G1) by
NatureServe and ‘‘critically endangered
in the state’’ (S1) by the North Carolina
Natural Heritage Program. The historical
and current impacts resulting from the
construction and operation of reservoirs
appear to be similar at each of these two
surviving occurrences of the species, as
does the threat posed by invasive,
nonnative vegetation. The species
appears to persist in areas subjected to
periodic water scouring of a velocity
sufficient to prevent the establishment
of other species without eliminating
previously established Solidago
plumosa plants (the age of which is
unknown). At the same time, although
dependent upon some level of flood
scouring, the species does not appear to
be tolerant of prolonged inundation as
it does not occur in frequently flooded
habitats. Therefore, the availability of
suitable habitat and the fate of all
known populations of this species are
primarily determined by the manner in
which the Narrows and Falls Reservoirs
are operated. To the extent that
operation of hydroelectric facilities
could be modified in the future to
enhance conditions for Solidago
plumose, the effects of reservoir
construction and operation are not
believed to be permanent or irreversible.
Thus, the magnitude of these threats
may be substantially reduced. In light of
all of these considerations, the
magnitude of threats to the species is
estimated to be ‘‘moderate to low.’’
One of the primary threats that
affected the species (construction of
Narrows and Falls Reservoirs and the
resulting inundation of suitable habitat)
has already occurred. However,
operation of these reservoirs continues
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to influence the habitat occupied by the
species, and may be facilitating (via a
reduction in the frequency and
magnitude of scouring events) the
establishment and spread of mimosa
(Albizia julibrissin) (an invasive,
nonnative shrub). Because mimosa is
already shading established Solidago
plumosa plants, it may potentially be
competing for seed germination and
seedling establishment sites. The threats
posed by lack of scouring and the
subsequent establishment and spread of
mimosa are ongoing and, therefore,
considered to be imminent. The threat
posed by the nonnative hybrid bush
honeysuckle (Lonicera x bella) is more
remote, as the species has not yet
established in habitats occupied by
Solidago plumosa. We conclude that the
threats affecting the species are of a
moderate to low magnitude, but are
imminent, leading to a listing priority
number of 8.
Summary of Listing Priority Changes in
Candidates
We reviewed the listing priority
number for all candidate species and are
changing the numbers for the following
species. Some of the changes reflect
actual changes in either the magnitude
or imminence of the threats, and in two
cases, reflect a change in the taxonomy
of the species. For some species, our
changes in the listing priority number
reflect efforts to ensure national
consistency as well as closer adherence
to the 1983 guidelines in assigning these
numbers, rather than a change in the
nature of the threats.
Mammals
Mazama pocket gopher (Thomomys
mazama ssp. couchi, glacialis, louiei,
melanops, pugetensis, tacomensis,
tumuli, and yelmensis)—Candidate
status applies to each of these eight
subspecies of Thomomys mazama, all of
which are associated with glacial
outwash prairies in western
Washington. We do not include other T.
mazama subspecies that occur in
Oregon and California (commonly
referred to as ‘‘western pocket gophers’’)
as candidate species. Except as
otherwise noted, the following
description applies to each of the
subspecies. Most populations are small,
isolated, and patchily distributed. There
are no historical data and scant
quantitative data on current
populations. Several populations are
now extirpated. Two, and possibly
three, of the subspecies may be extinct
(T. m. louiei, T. m. tacomensis, and T.
m. tumuli).
Threats include destruction and
alteration of prairie habitat due to
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development, altered fire regimes, and
encroachment of native and nonnative
plants; conflicts with military activities
and airport development and
maintenance activities; house cat
predation; consideration as agricultural
pests; and vulnerability to naturally
occurring, random events. The
magnitude of threats is high due to
patchy and isolated population
distributions in habitats highly desirable
for development and subject to a wide
variety of human activities that
permanently alter the habitat. There are
high and constant invasions of plant
species altering the quality of remaining
habitat. Loss of any of the subspecies
will reduce the genetic diversity and
likelihood of the continued existence of
the species in Washington. Threats are
imminent because many of those listed
above are ongoing. It is likely that the
extirpation of some populations and the
extinction of two, and possibly three,
subspecies are the result of one or more
of these threats affecting each of these
populations and subspecies. One
subspecies is threatened by gravel pits,
and two subspecies are located on
airports with planned development.
Because of the increased imminence of
threats, we changed the listing priority
number for each of the eight subspecies
of the Mazama pocket gopher from a 6
to a 3.
Palm Springs (Coachella Valley)
round-tailed ground squirrel
(Spermophilus tereticaudus chlorus)—
The Palm Springs round-tailed ground
squirrel is one of four recognized
subspecies of round-tailed ground
squirrels. The range for the Palm
Springs round-tailed ground squirrel
corresponds to the Coachella Valley
region in Riverside County, California.
Primary habitat for the Palm Springs
round-tailed ground squirrel in the
Coachella Valley is the mesquite sand
dune/hummock community. The
species also is found in smaller numbers
in creosote communities on sand dunes
and hummocks. Approximately 90
percent of the mesquite hummock
communities in the Coachella Valley are
estimated to have been lost since 1939,
a reduction from 3,363 hectares (8,309
acres) to 352 hectares (870 acres). Future
development threatens more mesquite
communities occupied by the Palm
Springs round-tailed ground squirrel.
The largest unprotected mesquite
community in Indio Hills was recently
developed, effectively eliminating a
large ground squirrel population. The
rapid growth of urban development in
the Coachella Valley is threatening
existing ground squirrel populations
with habitat fragmentation.
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A recent taxonomic study that
examined the morphology of this
subspecies as well as those of adjacent
populations of another subspecies (S. t.
tereticaudus) revealed that the original
classification of this subspecies may be
in question. Pelage (hair) color was
found to be different among the two
subspecies. In addition, this study also
discovered that putative S. t.
tereticaudus populations in Death
Valley, the western central region of the
Mojave Desert, and Borrego Valley were
more similar in pelage color to S. t.
chlorus in the Coachella Valley than
other S. t. tereticaudus populations from
the Colorado River region of eastern
Imperial and Riverside Counties. We are
awaiting peer review of this report
before we take action to reconsider
whether this subspecies is valid. In the
meantime, we are seeking funding to
pursue a genetic study that will
determine this species’ taxonomy based
on DNA. Based on our evaluation that
the threats pose an imminent risk of a
high magnitude, we changed the listing
priority number for this subspecies from
a 6 to a 3.
Washington ground squirrel
(Spermophilus washingtoni)—This
species is one of the smallest members
of the subgenus Spermophilus, and is
found within the shrub-steppe habitat of
the Columbia Basin ecosystem of
Washington and Oregon. The soil types
used by the squirrels are distributed
sporadically within the species’ range,
and have been seriously fragmented by
human development in the Columbia
Basin, particularly by conversion to
agricultural use. Where agriculture
occurs, little evidence of ground squirrel
use has been documented, and reports
indicate that ongoing agricultural
conversion eliminates Washington
ground squirrel habitat. The most
contiguous, least-disturbed expanse of
suitable Washington ground squirrel
habitat, and likely the densest
distribution of colonies within the range
of the species, occurs on the Boeing site
and Boardman Bombing Range in
Oregon, and on Federal and Stateowned land in Washington. However, in
Washington, recent declines in some
colonies have been precipitous and the
reasons for them are unknown. In 2001,
for instance, entire colonies of ground
squirrels were no longer occupied on
the Columbia National Wildlife Refuge
and Seep Lakes Management Area near
Othello, Washington, despite the State
protected status of the species in the
area. Current and potential threats to the
continuing survival of the species
include the following: habitat loss from
the conversion of potential and known
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habitat to agricultural use, predation,
recreational shooting, disease, potential
effects of pesticides, and potential
effects of drought on forage quality and
quantity. However, while the magnitude
of threats remains high for the
Washington ground squirrel, the
immediacy of threats has declined in
the past year. The majority of existing
colonies (in Oregon and throughout the
species’ current range) are located on
the Boardman Bombing Range and the
Boeing tract, which contain the largest
contiguous suitable Washington ground
squirrel habitat. Although Boardman
Bombing Range activities are not
certain, they are not expected to change
significantly in the foreseeable future.
In 2003, the largest threat to colonies
in Oregon was the imminent conversion
of the Boeing tract for agriculture. This
would have resulted in the permanent
loss of habitat for one of the largest
contiguous blocks of Washington
ground squirrels. However, in 2004, a
25-year Multi-Species Candidate
Conservation Agreement with
Assurances (CCAA) was signed by
Threemile Canyon Farms, The Nature
Conservancy, Portland General Electric,
Oregon Department of Fish and
Wildlife, and the Service. The parties
will implement habitat management,
operational modifications, and
conservation measures for four nonlisted species, including the Washington
ground squirrel, on approximately
93,000 ac (37,636 ha) enrolled in the
CCAA. Under this agreement, Threemile
Canyon Farms placed 22,600 ac (9,146
ha) of the Boeing tract into a permanent
Oregon Department of Fish and Wildlife
Conservation Easement (Boardman
Conservation Area). Also, Portland
General Electric identified 888 ac (356
ha) for management as part of the
Conservation Area for the duration of
the CCAA. The Boardman Conservation
Area will be managed by TNC with the
goal to maintain and improve where
feasible the integrity of existing native
communities and associated species
covered by the CCAA, including the
Washington ground squirrel. All but two
known sites and the majority of suitable
habitat on the Boeing tract are located
on the Boardman Conservation Area and
therefore are protected from irreversible
habitat modification. Based on our
current evaluation of threats, we
changed the listing priority number
from 2 to 5 for this species as the threats
are no longer imminent.
Birds
Spotless crake (Porzana tabuensis),
American Samoa Distinct Population
Segment (DPS)—The genus Porzana is
widespread in the Pacific, where it is
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represented by numerous islandendemic and flightless species (many of
which are extinct as a result of
anthropogenic disturbances) as well as
several common and cosmopolitan
species such as the common crake. The
spotless crake is found in the
Philippines, Australia, Fiji, Tonga,
Society Islands, Marquesas,
Independent Samoa, and American
Samoa. No subspecies are currently
recognized.
The status of populations in other
areas is not well known, but the species
is thought to be in decline throughout
the oceanic Pacific, with at least one
known extirpation (from the island of
Futuna). In American Samoa, the
population of the spotless crake is
restricted to the summit of Tau Island.
The only known population in
American Samoa co-occurs with
Norway rats (Rattus norvegicus), which
are known to prey on birds and their
eggs and young. The spotless crake is
particularly vulnerable because it is
small, nests on the ground, and on Tau
summit has no wetland refuge from
predators. Finally, this single
population, which existing survey data
suggest is a small population, is at risk
from stochastic occurrences such as
typhoons and inbreeding depression.
These threats affect the entire known
population of this species in American
Samoa, and are potentially lethal to
individuals. The magnitude of threats
facing the species is thus high, and
these threats are more imminent than
previously inferred because additional
surveys indicate that this species occurs
only as a single, small population in
American Samoa.
Although this species may use a wide
variety of habitats, wetland habitats may
be necessary for self-sustaining
populations of the crake to persist in the
presence of predators. Wetland habitats
are limited in American Samoa, and
enforcement of their conservation under
local and Federal law is not consistent.
The listing priority number for the
spotless crake is changed from 6 to 3
because surveys on Tau over the past
several years have failed to yield
evidence of this species in locations
other than the summit, no observations
of this species have been made during
extensive, ongoing surveys of birds
elsewhere in American Samoa, and the
threat from rat predation is ongoing.
Friendly ground-dove (Gallicolumba
stairi stairi)—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
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French Polynesia, and G. stairi is
endemic to Samoa, Tonga, and Fiji. All
six species have some level of
threatened status on the International
Union for Conservation of Nature and
Natural Resources (IUCN) Red List.
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
morphological differences between the
two are minimal. In American Samoa,
the friendly ground-dove has been
found on the islands of Ofu and Olosega
(Manua Group).
Of the primary threats to the
subspecies (predation by nonnative
species, poaching and habitat loss), only
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 increases in the
population. Predation by introduced
species has played a significant role in
reducing and limiting 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). Consistent monitoring
using a variety of methods over the last
5 years yielded few observations 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 ground-dove is limited to steep,
rocky slopes; areas that are not common
in American Samoa. Threats to this
subspecies have not changed over the
past year, but to better reflect the fact
that threats due to small population size
and nonnative predators are imminent,
we revised the listing priority number
from a 6 to a 3.
Kauai creeper (Oreomystis bairdi)—
The Kauai creeper, or akikiki, is a small
Hawaiian honeycreeper found only on
the island of Kauai, Hawaii, with no
described subspecies. The species is
known to be presently facing the
primary threats of disease (avian
malaria) and habitat degradation and
loss. These threats have persisted over
several decades, and are affecting a large
proportion of the population.
The mosquito vector of avian malaria
has been found throughout the range of
elevations over which the creeper
occurs, and malaria transmission occurs
at least periodically over the species’
entire range. The area of forest where
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malaria is endemic is likely to increase
with global climate change.
Efforts are underway to reduce habitat
loss through control of invasive
nonnative plants in some areas, but
there is no weed control in most of the
range of the Kauai creeper, and habitat
loss is already occurring. Also, there are
currently no efforts to control habitat
damage by feral ungulates within the
range of the Kauai creeper.
A large scale survey in 2000 showed
that in the last 30 years the estimated
population declined nearly 80 percent
(from 6,832 ± 966 to 1,472 ± 680 birds),
the range decreased approximately 60
percent (from 21,750 to 8,896 acres
(8,800 to 3,600 hectares)), and the
species has disappeared from much of
the periphery of its range. The listing
priority number for the Kauai creeper is
changed from a 5 to a 2 because the
threats facing the species are of a high
magnitude and are imminent.
Yellow-billed cuckoo, Western
Continental U.S. DPS (Coccyzus
americanus)—While the cuckoo is still
relatively common east of the crest of
the Rocky Mountains, biologists
estimate that more than 90 percent of
the bird’s riparian (streamside) habitat
in the West has been lost or degraded.
These modifications, and the resulting
decline in the distribution and
abundance of yellow-billed cuckoos
throughout the western states, are
believed to be due to conversion to
agriculture; grazing; competition from
nonnative plants, such as tamarisk; river
management, including altered flow and
sediment regime; and flood control
practices, such as channelization and
bank protection. Riparian habitat is
continuing to be destroyed through land
use conversion and grazing. Threats to
the yellow-billed cuckoo have not
changed over the past year, but to better
reflect the fact that threats are
imminent, we revised the listing priority
number from a 6 to a 3 for this DPS.
Many-colored fruit-dove (Ptilinopus
perousii perousii)—Two subspecies of
the many-colored fruit-dove exist. One,
P. p. perousii, is found in American
Samoa, within the four main islands of
Tutuila, Olosega, Ofu, and Tau, and
Independent Samoa. Another
subspecies, P. p. mariae, is found in Fiji
and Tonga.
The primary threats to P. p. perousii,
loss of the native banyan trees on which
it depends, poaching, and predation by
nonnative mammals, are thought to
occur at levels insufficient to have a
detrimental effect on the species’
population in American Samoa. This is
demonstrated by the fact that 5 years of
extensive and intensive monitoring
indicate an increase in the detected
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relative abundance of many-colored
fruit-doves in American Samoa. This
trend may have been interrupted by
Typhoon Heta in January of 2004, when
damage to their primary food plants, the
two species of native banyan trees, may
have altered the doves’ foraging to make
them more vulnerable to the
opportunistic poaching that typically
takes place after typhoons (Craig et al.
1994).
At present, no disturbance other than
typhoons is known to affect the
abundance, distribution, or productivity
of native banyans in American Samoa.
Loss of native rainforest harboring these
banyans and, presumably, the nesting
habitat for the many-colored fruit-dove
is not currently considered to be taking
place at a rate that poses a severe or
imminent risk to the many-colored fruitdove, and poaching of this species is
thought to be an extremely rare
occurrence.
Predation by introduced species has
played a significant role in limiting and
extirpating populations of island birds
in the Pacific and other locations
worldwide (Atkinson 1977, 1985; Moors
and Atkinson 1984). Nonnative
predators known to occur in the range
of the many-colored fruit-dove in
American Samoa that could be a
significant threat to this arboreal-nesting
bird are black rats (R. rattus), Norway
rats (R. norvegicus), and feral cats (Felis
catus). However the continued existence
of this species and the recently
documented increase in its abundance,
suggest that predation, while a potential
threat, is not of a high-magnitude. The
total population size of the manycolored fruit-dove is unknown, but may
number up to a few hundred pairs.
In Independent Samoa, the manycolored fruit-dove may be more
abundant than it is in American Samoa,
but this difference likely reflects
difference in island size—the main
islands of Independent Samoa are both
an order of magnitude larger than the
islands of American Samoa—and the
greater abundance in Independent
Samoa of the two native figs, Ficus
prolixa and F. obliqua, that are the
preferred food of this fruit-dove.
However, ongoing deforestation
(potentially exacerbated by severe
storms) and hunting are considered to
threaten the many-colored fruit-dove in
Independent Samoa, and this
subspecies’ status there is described as
‘‘Conservation Concern.’’ We changed
the listing priority number for the manycolored fruit-dove from 6 to 12 because
the overall magnitude of threats is
moderate to low and these threats are
not imminent.
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Xantus’s murrelet (Synthliboramphus
hypoleucus)—Xantus’s murrelet is a
small seabird of the Alcid family that
occurs along the western coast of North
America in the United States and
Mexico. Xantus’s murrelet populations
in the United States and Mexico appear
to have declined due to a wide variety
of threats, with substantial declines
evident at the largest known breeding
population and extirpations on three of
the Mexican islands. Data from the
largest breeding population on Santa
Barbara Island in the United States
indicated a dramatic decline (as much
as 70 percent from 1977 to the mid1990s); data from other islands are
scarce.
Although the decline in Xantus’s
murrelet populations appears to have
been substantial, some of the largest
threats are being addressed, and, to
some degree, ameliorated in the United
States. For example, although predation
is a large contributor to the current low
population numbers of the Xantus’s
murrelet, it does not pose as imminent
a threat as it once did. Cats and rats
have been removed from many of the
islands where they once occurred.
Anacapa Island implemented a rat
eradication program in 2001 that seems
to have been successful in removing that
nonnative predator of the Xantus’s
murrelet. Rats were eradicated in 1994
from San Roque Island. Although the
nonnative herbivores have been absent
from Santa Barbara Island since the late
1950s, their presence facilitated the
introduction of non-native grasses,
which continue to exist and spread on
that island. The conversion of native
habitat to nonnative grassland that has
occurred on Santa Barbara Island poses
a threat to the population of Xantus’s
murrelet due to the fact that the island
is only one square mile in size and
holds the majority of the nesting
population in California. Introduction of
nonnative grasses has modified the
habitat. Such habitat modification is
thought to have increased the endemic
deer mouse (Peromyscus maniculatus
elusus) population, a native predator of
Xantus’s murrelet eggs.
The Service has been working with
the State of California, National Park
Service, and National Marine Fisheries
Service to address the threats of light
pollution and human disturbance. Many
nocturnal birds are attracted to the
lights of commercial fishing vessels and
Xantus’s murrelets and other seabirds
become exhausted from continual
attraction and fluttering near lights or
collide with lighted vessels, the impact
resulting in injury or death. Chicks have
been documented to separate from their
parents due to vessel lights, often
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resulting in death as chicks are
dependent on parents for survival.
Additionally, squid boats operate in
shallow waters close to Xantus’s
murrelet breeding colonies in the
California Channel Islands. Increased
predation on Xantus’s murrelets by
Western gulls (Larus occidentalis) and
barn owls (Tyto alba) as a result of
lighting, particularly from squid boats,
near breeding colonies has been
documented. To address the threat from
light pollution, the California
Department of Fish and Game
implemented regulations to require
shielding and limit wattage of lights
used by boats conducting nighttime
fishing activities. Although these
regulations do not remove the negative
effects of this activity, they likely have
resulted in a reduction of the impacts.
Although not likely responsible for the
species’ current low numbers, oil
pollution may pose a potential threat to
the survival of the Xantus’s murrelet
population.
Despite actions to address some of the
threats to this species, a recent proposal
by ChevronTexaco Corporation to build
a liquid natural gas (LNG) facility 600
meters offshore Islas Los Coronados in
Baja California, Mexico, poses a threat
to the survival of the Xantus’s murrelet.
The Los Coronados islands support the
largest known breeding population of
Xantus’s murrelets in the world. The
construction and operation of the
proposed LNG facility at Islas Los
Coronados would increase levels of
disturbance to Xantus’s murrelets.
Sources of disturbance include: (1)
Bright lights at night from the facility
and visiting tanker vessels; (2) noise
from the facility; (3) noise from
helicopters visiting the facility; (4)
ingress and egress of tanker vessels; and
(5) other vessels transporting personnel
and supplies. These factors would have
a serious impact on the islands’
population of Xantus’s murrelets, and,
taken together, the cumulative
disturbance caused by this proposed
facility would have substantial negative
consequences for the colony.
Additionally, there are potential
impacts to the Xantus’s murrelet prey
base due to increased seawater
chlorination resulting from this facility.
The ocean waters around Islas Los
Coronados are highly productive and
very important foraging areas for
breeding, migrant, and wintering
seabirds such as the Xantus’s murrelet.
The loss of large numbers of prey could
be detrimental to seabirds that depend
on Islas Los Coronados for foraging at
various times of year. Degraded water
quality around Islas Los Coronados may
also result from this project, such as
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from the seawater chlorination process.
A gas spill from the facility or pipeline
could have substantial negative effects
on the Xantus’s murrelet. Due to the
now imminent threats from the
proposed LNG facility, we changed the
listing priority number for this species
from a 5 to a 2.
Amphibians
Black Warrior waterdog (Necturus
alabamensis)—The Black Warrior
waterdog 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, however, as
limited attention was given to this
species between its description in 1937
and the 1980’s. There are a total of 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 1990’s 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. An additional
threat to the Black Warrior waterdog is
the creation of large impoundments that
have flooded thousands of acres of its
habitat. These impoundments are likely
marginal or unsuitable habitat for the
salamander. Threats to the Black
Warrior waterdog have not changed over
the past year, but to better reflect the
fact that threats from the pervasive
water quality degradation in the Black
Warrior Basin are imminent, we
changed the listing priority number
from a 5 to a 2 for this species.
Ozark hellbender (Cryptobranchus
alleganiensis bishopi)—Since the
species was elevated to candidate status
in 2001 (66 FR 54808), the known
threats have increased. In particular,
recreational pressures on Ozark
hellbender rivers have increased
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substantially on an annual basis. The
Missouri Department of Conservation
reports that gigging popularity and
pressure has increased, which presents
a significant threat to hellbenders
during the breeding season as they tend
to move greater distances and
congregate in small groups where they
are an easy target for giggers. Canoe,
kayak, and motor/jet boat traffic has
increased in recent years on the Jacks
Fork, Current, Eleven Point, and North
Fork Rivers. The popularity of these
float streams has grown to the point that
the National Park Service is considering
alternatives to reducing the number of
boats that can be launched daily by
concessionaires, but no change has been
adopted and even if one is, floating will
still occur. Horse trail rides are
extremely popular along both the Jacks
Fork and Current National Scenic
Rivers. In 2003, the Missouri
Department of Natural Resources added
a 7-mile stretch of the Jacks Fork River
to the 303(d) list of impaired waters for
organic wastes (fecal coliform)
immediately downstream from a
commercial horse trail ride outfitter.
To date, nothing has been done to
reduce or ameliorate ongoing threats to
Ozark hellbenders. The Ozarks region
continues to experience rapid
urbanization, expansion of industrial
agricultural practices such as
concentrated animal feeding operations
(chickens, turkeys, hogs, cattle), and
logging. No laws are in place that
preclude livestock from grazing in
riparian corridors and resting in or
along streams and rivers. Missouri is the
second largest beef cattle producing
state in the nation, with the majority of
animal units produced in the Ozarks.
Both Arkansas and Missouri are the
leading States in poultry production.
The fact that the majority of the Ozarks
region in Missouri and Arkansas is
comprised of karst topography (caves,
springs, sinkholes, and losing streams)
further complicates the containment
and transport of potential contaminants.
In short, the abundance of treatment
facilities and lack of adequate treatment
facilities or practices for both human
and livestock waste poses a significant
and ever increasing threat to aquatic
ecosystems. The decrease in Ozark
hellbender range and population size
and the shift in age structure are likely
caused by a variety of historic and
ongoing activities. The primary cause of
these trends is habitat destruction and
modification through impoundment,
channelization, siltation, and water
quality degradation from a variety of
sources, including industrialization,
agricultural runoff, mine waste, and
timber harvest. Overutilization of
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hellbenders for commerce and scientific
purposes is also likely contributing to
their decline. The regulations in place
that could prevent these impacts,
including the Clean Water Act and State
laws, have been inadequate in
preventing Ozark hellbender declines to
this point. Finally, most of the
remaining Ozark hellbender populations
are small and isolated, making them
vulnerable to individual catastrophic
events and reducing the likelihood of
recolonization after localized
extinctions. Due to substantial increases
in recreational pressures on Ozark
hellbender rivers on an annual basis, we
changed the listing priority number for
this subspecies from a 6 to a 3.
Clams
Georgia pigtoe (Pleurobema
hanleyanum)—The Georgia pigtoe was
historically found in shallow runs and
riffles in large creeks and rivers of the
Coosa River drainage system in
Alabama, Georgia, and Tennessee. The
species is currently known to exist in
localized portions of the upper
Conasauga River in Murray and
Whitfield Counties, Georgia, and in a
short reach of the Coosa River below
Terrapin Creek, Cherokee County,
Alabama. The Georgia pigtoe is very
rare, with only a few observations of
living animals over the past 15 years.
Impoundment and pollution are
implicated in the decline and
disappearance of the species. We
changed the listing priority of the
Georgia pigtoe from a 5 to a 2 due to
rarity and continued lack of success into
locating living animals.
Snails
Bonneville pondsnail (Stagnicola
bonnevillensis)—The Bonneville
pondsnail occupies four spring pools
north of the Great Salt Lake in Box Elder
County, Utah (Horse Spring B, Horse
Spring B South, Pipe Spring, and
Shotgun Spring). While the total
number of individuals is unknown, the
total occupied habitat is less than one
hectare. Two previous threats to this
species now appear to have been
resolved. Leaks from petroleum
pipelines in the area have occurred in
2000 and 2002; however, Chevron
Pipeline (which has responsibility for
operation and maintenance of the
pipelines) has addressed potential
threats from pipeline leaks with internal
integrity inspections and alerts prior to
leakage. Consequently, potential
pipeline leaks are not a current threat.
Intensive, unregulated grazing can
degrade the habitat of aquatic species,
including Stagnicola bonnevillensis, but
the springs where this species occurs
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have been fenced to restrict livestock
use and this is not a current threat.
Current threats to this species include
perchlorate and trichloroethelene (TCE)
contamination from ATK Thiokol, Inc.
(Thiokol). Until recently, Thiokol
disposed of waste products such as
perchlorate and TCE in an area 6.5 km
(4 mi) upstream from the pondsnail’s
habitat, within the same hydrologic
ground water gradient as the occupied
snail habitat. Contaminated soils have
been removed and the area capped to
prevent further contamination.
Groundwater sampling indicates that
the 10 µg/l isoline of the TCE plume is
0.5 km (0.3 mi) north of Shotgun and
Pipe Springs. The 100 µg/l isoline of the
TCE plume is 2.4 km (1.5 mi) northwest
of Shotgun Spring. The 1000 µg/l isoline
of the TCE plume is 3.5 km (2.2 miles)
northwest of Shotgun Spring. Levels of
percholate measured in June 2004 range
from 6.6 µg/liter in Fish Spring to 287
µg/liter in Pipe Spring. The acute
toxicity of TCE and perchlorate to
Stagnicola bonnevillensis is under
investigation, but both substances are
potentially lethal to most wildlife
species. The current levels of TCE and
perchlorate in the occupied springs and
the approaching groundwater plume are
of concern for the future of this species
and its habitat. Thiokol is taking
corrective action to identify and
remediate groundwater contamination
through a Corrective Action Plan (an
updated groundwater model and risk
assessments are to be completed in May
2005 under this plan). Bioassay studies
are being initiated to determine the
effect of these contaminants on the snail
and its habitat.
Although the range of this species is
highly restricted and the only known
habitat is currently threatened by
chemical contamination of the ground
water, we consider the following actions
that are addressing these threats to be
significant enough to have reduced the
magnitude of threats from high to
moderate: discontinued disposal of
wastes in an unlined impoundment,
removal of contaminated soil,
installation of a cap to prevent
infiltration of water into soils beneath
impoundment, monitoring of
downgradient groundwater for
contamination, implementation of a
Corrective Action Plan to characterize
and remediate groundwater
contamination, implementation of a site
management plan, and development of
a groundwater model and risk
assessment. Thus, we changed the
listing priority from a 2 to an 8.
Additionally, the Utah Division of
Wildlife Resources is currently drafting
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a Conservation Agreement and Strategy
for this species.
Interrupted (Georgia) rocksnail
(Leptoxis foremani (downei))—
Interrupted rocksnails historically
occurred in shoals, riffles, and reefs of
small to large rivers in the Coosa River
Basin of Alabama and Georgia. Today,
only a single surviving natural
population is known from a short reach
of the Coosawattee River, Georgia.
During a 1999 census, 10–45 interrupted
rocksnail snails per square meter were
found in this reach. In 2004, a 6 manhour search was required to find 20
individuals. Water quality is suspected
as the cause of decline. A captive colony
of approximately 200 snails was
established at the Tennessee Aquarium
Research Institute (TNARI) in 2000 for
study and propagation. During the
winter of 2003, the Alabama Department
of Conservation and Natural Resources
released about 3000 juvenile interrupted
rocksnails from the TNARI colony into
the Coosa River above Wetumpka,
Elmore County, Alabama. The status of
this reintroduction is currently
unknown. We changed the listing
priority number for the interrupted
rocksnail from a 5 to a 2 due to the
recent precipitous decline of the only
known naturally surviving population
in the Oostanaula River.
Newcomb’s tree snail (Newcombia
cumingi)—A tree-dwelling species,
Newcomb’s tree snail belongs to the
snail family, Achatinellidae. The
species is endemic to the island of
Maui, where it is currently known from
a single remaining population. This
species is currently threatened by
habitat loss and modification and by
predation from nonnative predatorial
snails. Because the threats are of a high
magnitude and are now considered
imminent because they are ongoing, we
changed the listing priority number
from a 5 to a 2.
Crustaceans
Anchialine pool shrimp (Vetericaris
chaceorum)—Vetericaris chaceorum 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 one population on the
island of Hawaii. The primary threats to
this species are habitat loss and
predation from nonnative fish species.
We changed the listing priority number
for this species from a 2 to a 1 as this
species is in a monotypic genus. The
threats remain imminent and of a high
magnitude.
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Flowering Plants
Bidens amplectens (Kookooalu)—This
species is an erect perennial or
facultatively annual herb found in
mixed lowland dry shrubland/grassland
on Oahu, Hawaii. This species is known
from one population of 500 to 1,000
individuals in the Waianae Mountains.
Threats to the species include nonnative
plants that increase the fuel load and
fire threat, and compete for habitat. We
have changed the listing priority
number for this species from 5 to 2
because the threats are ongoing, and
therefore, imminent.
Bidens campylotheca ssp. pentamera
(Kookooalu)—This species is an erect,
perennial herb found in CheirodendronMetrosideros polymorpha montane wet
forest on Maui, Hawaii. This subspecies
is known from 11 populations with a
total of approximately 500 individuals,
and is restricted to the island of Maui.
Threats to the species include ungulates
that eat this plant and degrade and
destroy habitat, and by nonnative plants
that compete for habitat. We have
changed the listing priority number for
this species from 6 to 3 because the
threats are ongoing, and therefore,
imminent.
Bidens micrantha ssp. ctenophylla
(Kookooalu)—This species is an erect,
perennial herb found in open mixed
shrubland to dry Metrosideros forest on
the island of Hawaii, Hawaii. This
species is endemic to the island of
Hawaii, where it is restricted to an area
of less than 10 square miles (26 square
kilometers). This species is known from
four populations totaling approximately
3,000 individuals, the majority of which
occur in only two populations. Threats
to the species include land development
and nonnative plants such as
Pennisetum setaceum and Leucana
leucocephala, which degrade habitat,
possibly contributing to fire. We have
changed the listing priority number for
this species from 6 to 3 because the
threats are ongoing, and therefore,
imminent.
Brickellia mosieri (Florida brickellbush)—This white-flowered, narrowleaved herb in the aster family occurs in
central and southern Miami-Dade
County, Florida, from Southwest 120th
Street to Florida City. It is found
exclusively in pine rocklands, where it
tends to occur in areas within open
shrub canopy and exposed limestone
with minimal organic litter.
Approximately 99 percent of the former
habitat has been converted to urban
areas or farmland. Seventeen
occurrences currently are confirmed in
remnant blocks of habitat; thirteen are
owned or managed by Miami-Dade
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County and the others are privately
owned. Of the known occurrences most
contain a low density of plants; only
two occurrences are believed to contain
more than 1,000 individuals and the
total population is estimated to be no
more than 10,000 individuals, but more
likely to be 5,000 to 7,000 individuals.
There is little likelihood of finding
significantly more populations. Fire
suppression is one of the greatest threats
to this species. Fire is required to
maintain the pine rockland community
but with fire suppression, hardwoods
eventually increase and shade out
understory species such as Brickellia
mosieri. The other most significant
threat is exotic plants. Throughout its
range the species also is threatened by
invasive exotic plants, and even if
effective control methods are found for
existing invasive exotic plants,
additional invasive exotic plants are
expected to emerge since areas near the
managed pine rockland contain exotic
species and can act as a seed source of
exotics allowing them to continue to
invade the pine rockland. However, 13
of the 17 sites are on conservation lands
where control of invasive exotic species
is being implemented, as well as
controlled burns. Overall, the
magnitude of threats to the Florida
brickell-bush is moderate. The threats
are also ongoing and therefore,
imminent. Thus, we have revised the
listing priority number from a 5 to an 8.
Calamagrostis expansa (no common
name)—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, Calamagrostis expansa
was restricted to wet forest and bogs on
Maui. Currently, this species is known
from 100 populations of 1 or 2
individuals each on Maui, and was
recently discovered in 5 populations
totaling approximately 300 individuals
on the island of Hawaii. The species is
currently threatened by pigs that
degrade and destroy habitat and
nonnative plants that outcompete and
displace them. We have changed the
listing priority number for this species
from 5 to 2 since the threats are ongoing,
and therefore, imminent.
Calamagrostis hillebrandii (no
common name)—This species is a
slender, short-rhizomatous perennial
found in Metrosideros-Machaerina
montane wet bog or ohia-kuolohiaOreobolus (Metrosideros-RhynchosporaOreobolus) mixed bog on Maui, Hawaii.
This species is known from two
populations of about 500 individuals,
restricted to the bogs of West Maui,
although it was formerly found on the
island of Molokai as well. This species
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is currently threatened by pigs that
degrade and destroy habitat and
nonnative plants that outcompete and
displace them. We have changed the
listing priority number for this species
from 5 to 2 since the threats are ongoing,
and therefore, imminent.
Calochortus persistens (Siskiyou
mariposa lily)—The Siskiyou mariposa
lily is a narrow endemic that is
restricted to two disjunct ridge tops in
the Klamath-Siskiyou Range on the
California-Oregon border. In California,
this species is currently found at 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 GunsightHumbug Ridge. In 1998, five Siskiyou
mariposa lily plants were discovered 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 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 California
population, affecting 90 percent of the
known lily habitat. Forest Service staff
and the Klamath-Siskiyou Wildlands
Center cite competition with dyer’s
woad as a significant and chronic threat
to the survival of Siskiyou mariposa lily.
The combination of restricted range,
extremely low numbers (five plants) in
one of two disjunct populations, poor
competitive ability, short seed dispersal
distance, slow growth rates, low seed
production, apparently poor survival
rates in some years, and competition
from exotic plants threaten the
continued existence of this species.
However, as a result of information
gained during the 2003 field season, the
listing priority number has been
changed from 2 to 5. Our previous rating
was based on the reported results of
unpublished demographic research that
showed an absence of reproduction,
leading the Service to rate the
immediacy of threats as imminent.
However, during last season’s extensive
survey, Klamath National Forest staff
observed juvenile plants across the
California range of C. persistens. For
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this reason, we have revised the
immediacy of threats to nonimminent.
Because none of the threats to C.
persistens are anticipated to cause
extinction in the immediate future and
because the nonimminent threats are of
a high magnitude, we assigned a listing
priority number of 5 to this species.
Canavalia napaliensis (Awikiwiki)—
This species is a perennial climber
found in open dry sites and coastal
strand, diverse lowland dryland/mesic
forest to mixed mesophytic forest on
Kauai, Hawaii. Canavalia napaliensis is
known from three populations totaling
several hundred individuals in a small
section of the Na Pali coast. This species
is currently threatened by goats that eat
this plant and degrade and destroy
habitat, and by nonnative plants that
outcompete and displace them. We have
changed the listing priority number for
this species from 5 to 2 since the threats
are ongoing, and therefore, imminent.
Chamaesyce deltoidea ssp. pinetorum
(Pineland sandmat)—This small,
upright, round-leaved herb belonging to
the spurge family is known only from
the southern portion of the Miami Rock
Ridge in Southern Miami-Dade County,
Florida. This species occurs in tropical
pine woods on limestone rock (rock
pinelands). It is shade intolerant and
requires periodic prescribed fires to
reduce competition from woody
vegetation. The total number of plants
has been estimated to be fewer than
10,000. Plants occur on conservation
lands at Everglades National Park and
seven relatively small pinelands owned
by Miami-Dade County, one private
preserve, and a governmental nonconservation site. Additionally, fewer
than 1,000 plants are estimated to occur
at less than 10 privately owned
unprotected sites. The most serious
threats are lack of fire in small urban or
near-urban preserves and invasive pest
plants. Despite effective exotic pest
plant management in Everglades
National Park and on Miami-Dade
County lands, the pest plant threats
remain, and new problems, such as Old
World climbing fern, are emerging.
While there are inherent difficulties in
maintaining small pinelands and the
exotic pest plant threats are serious,
overall, the threats are moderate in
magnitude; the largest population
occurs on Everglades National Park
where invasive species are being
actively controlled and fire is being
used to maintain habitat for this species.
The threats are imminent since they are
ongoing. Therefore, we are revising the
listing priority number for the pineland
sandmat from 6 to 9.
Chamaesyce eleanoriae (Akoko)—
This species is a small shrub found on
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steep slopes and cliffs, in MetrosiderosDiospyros lowland mesic forest and
Eragrostis variabilis coastal dry cliffs on
Kauai, Hawaii. This species is known
from 10 populations totaling less than
500 individuals. Described in 1996, it is
found only in and around Kalalau
Valley rim, along the Na Pali Coast on
the island of Kauai. Although it was
only discovered in 1992, a decline in
numbers has already been observed. The
species is threatened by goats and rats
that eat this plant and degrade and
destroy habitat, and by nonnative plants
that outcompete and displace it. We
have changed the listing priority
number for this species from 5 to 2 since
the threats are ongoing, and therefore,
imminent.
Chamaesyce remyi var. kauaiensis
(Akoko)—This species is a shrub found
in wind-swept shrubland and adjacent
forest patches dominated by
Metrosideros and Syzygium on Kauai,
Hawaii. Chamaesyce remyi var.
kauaiensis is known from four or five
populations totaling 300 to 400
individuals. This variety is found only
in the Wahiawa and Blue Hole areas on
the island of Kauai. This species is
threatened by goats and pigs that eat
this plant and degrade and destroy
habitat, by the two-spotted leafhopper
that damages leaves and may spread
plant viruses, and by nonnative plants
that outcompete and displace it. We
have changed the listing priority
number for this species from 6 to 3 since
the threats are ongoing, and therefore,
imminent.
Chamaesyce remyi var. remyi
(Akoko)—This species is a perennial
shrub found in wet Metrosideros
polymorpha-Dicranopteris linearis
montane mesic forest on Kauai, Hawaii.
Chamaesyce remyi var. remyi is known
from at least 10 populations totaling 500
to 1,000 individuals. Hybrids of C.
remyi and C. sparsiflora have been
found near the margins of Wahiawa Bog,
Kauai. This species is threatened by
goats and pigs that eat this plant and
degrade and destroy habitat, by the twospotted leafhopper that causes leaf
damage and may spread viruses, and by
nonnative plants that outcompete and
displace it. We have changed the listing
priority number for this plant variety
from 6 to 3 since the threats are ongoing,
and therefore, imminent.
Charpentiera densiflora (Papala)—
This species is a tree found in Diosporus
sandwicensis-dominated lowland mesic
forest, extending into diverse mesic
forest on Kauai, Hawaii. Charpentiera
densiflora is known from 10
populations totaling approximately 200
individuals, restricted to an area of less
than 10 square miles (26 square
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kilometers) in the Na Pali coast area on
the island of Kauai. The threat to the
species is feral goats that degrade and
destroy habitat. We have changed the
listing priority number for this species
from 5 to 2 since the threats are ongoing,
and therefore, imminent.
Chromolaena frustrata (Cape Sable
thoroughwort)—This blue-flowered herb
of the aster family presently occurs in
Monroe County, Florida, at scattered
locations in the Florida Keys and
Everglades National Park near the
Flamingo Visitors Center. Within the
past 30 years, it was also observed
slightly farther east in Everglades
National Park in Miami-Dade County. In
the Florida Keys (Monroe County), Cape
Sable thoroughwort occupies rock
barrens and edges of tropical hardwood
hammocks. Populations of Cape Sable
thoroughwort on public conservation
lands are small. Everglades National
Park has fewer than 150 plants (remote
areas have not yet been surveyed); Boca
Grande Key, Lignumvitae Key, Long
Key, Upper Matecumbe Key have
approximately 25, 81, 200, and 18
plants respectively. The species is also
present at two privately owned sites
(Long Key and Big Munson Island) in
the Keys. Approximately 162 plants are
on private land at Long Key. The only
large population of Cape Sable
thoroughwort (consisting of thousands
of plants) is on a privately owned island
near Big Pine Key. The abundance of
Cape Sable thoroughwort here is
probably due to Hurricane Georges in
1998, which opened the island’s tree
canopy. While the 1998 hurricane
benefited one population, a more severe
storm could have very different effects.
The listing priority has been increased
to reflect the high and imminent risk of
extinction due to small population size,
combined with the risk of loss of
populations from exotic pest plants
(especially Brazilian pepper) through
changes in community structure and
competition, hurricanes, and other
disturbances (e.g. from trail
construction). Therefore, we changed
the listing priority number for the Cape
Sable thoroughwort from a 5 to a 2.
Cyanea calycina (Haha)—This species
is an unbranched shrub found in
Metrosideros-Dicranopteris montane
wet forest and wet gulches and
streambanks on Oahu, Hawaii. This
species is known from about 20
populations with a combined total of
200 or more individuals. Threats to the
species include pigs and goats that
degrade and destroy habitat, rats and
slugs that directly prey upon it, and
nonnative plants that outcompete and
displace it. We have changed the listing
priority number for this species from 5
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to 2 since the threats are ongoing, and
therefore, imminent.
Cyanea kunthiana (Haha)—This
species is a shrub found in closed
Metrosideros polymorpha montane wet
forest on Maui, Hawaii. The historic
range of Cyanea kunthiana was wet
forest on the island of Maui. While there
are no historic records of numbers of
populations or individuals, qualitative
accounts indicate that the species was
not uncommon. Currently, this species
is declining throughout its range and is
known from approximately 20
populations with a combined total of
several hundred individuals. Threats to
the species include pigs, rats, and slugs
that eat this plant and degrade and
destroy habitat, and nonnative plants
that outcompete and displace it. We
have changed the listing priority
number for this species from 5 to 2 since
the threats are ongoing, and therefore,
imminent.
Cyanea lanceolata (Haha)—This
species is a shrub found in Acacia koaMetrosideros polymorpha lowland
mesic forest on Oahu, Hawaii. This
species is known from 20 populations
with a combined total of less than 300
individuals. Threats to the species
include pigs, rats, and slugs that prey
upon, degrade and destroy habitat, and
nonnative plants that outcompete and
displace it. We have changed the listing
priority number for this species from 5
to 2 since the threats are ongoing, and
therefore, imminent.
Cyanea tritomantha (Aku)—This
species is a palm-like tree found in
closed Metrosideros-Cibotium montane
wet forest on the island of Hawaii,
Hawaii. This species is known from four
to five populations with a total of 100
to 500 individuals in Olaa and Kau on
the island of Hawaii. Threats to the
species include pigs, rats, and slugs that
eat this plant and degrade and destroy
habitat, and nonnative plants that
outcompete and displace it. We have
changed the listing priority number for
this species from 5 to 2 since the threats
are ongoing, and therefore, imminent.
Cyrtandra kaulantha (Haiwale)—This
species is a shrub found in moist
wooded gulches in dense shade on
Oahu, Hawaii. This species is known
from seven populations with a total of
37 individuals along the Waiahole Ditch
Trail on the island of Oahu. Threats to
the species include pigs and slugs that
eat this plant and degrade and destroy
habitat. We have changed the listing
priority number for this species from 5
to 2 since the threats are ongoing, and
therefore, imminent.
Cyrtandra oenobarba (Haiwale)—This
species is a low, decumbent, fleshy,
subshrub found in Metrosideros
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polymorpha-Dicranopteris linearis
lowland wet forest on Kauai, Hawaii.
The historic range of this species was
throughout the island of Kauai. While
there are no historic records of numbers
of populations or individuals,
qualitative accounts indicate that the
species was relatively widespread and
abundant. Recent surveys show that the
species is now limited to 10 or more
populations with a combined total of
200 to 500 individuals in only three
small areas on the island of Kauai.
Threats to the species include pigs that
eat this plant and degrade and destroy
habitat, and nonnative plants that
outcompete and displace it. We have
changed the listing priority number for
this species from 5 to 2 since the threats
are ongoing, and therefore, imminent.
Dalea carthagenensis var. floridana
(Florida prairie clover)—This shrubby
pea is restricted to south Florida, where
it is found in edges of rockland
hammock and pine rockland, coastal
upland, and marl prairie. Fire is likely
very important for this species since
Florida prairie clover probably does not
tolerate shading by hardwoods in the
absence of periodic fires. Two colonies
occur in the Big Cypress National
Preserve (Collier and Monroe Counties),
two colonies occur at the Deering Estate
at Cutler (managed by Miami-Dade
County), and one colony exists at the R.
Hardy Matheson Preserve (Miami-Dade
County). Although this species
potentially might be rediscovered at still
existing Miami area sites where it was
once collected (such as Crandon Park on
Key Biscayne, the Castellow Hammock
Environmental Education Center, and
the edge of Everglades National Park),
species experts believe this is unlikely.
The estimated total population of
Florida prairie clover is 200 to 300
plants. Even if all the plants were in a
single locality, they probably would not
constitute a viable population. The State
has designated the species as
endangered, but this listing provides
little or no habitat protection beyond
disclosure of impacts. Threats to this
plant developed over the course of the
twentieth century as most of its
geographic range in Miami-Dade County
became urbanized, leaving only small
remnants of pine rocklands. Fire
suppression and invasive exotic plants
are the greatest threats to this species. In
the absence of fire, hardwoods
eventually shade out understory species
like Dalea carthagenesis var. floridana.
Conducting prescribed fires in urban
areas where the small sites exist is
difficult but there has been some
success at the Charles Deering Estate
and R. Hardy Matheson Preserve. Exotic
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(i.e., nonnative) plants are widespread
and difficult to control. There have been
some efforts to remove the exotic plants
at the smaller sites, but the methods
used are not feasible at the large Big
Cypress National Preserve. The small
remaining populations of the species
also are extremely vulnerable to the
effects of hurricanes. Overall, our
review of the status of this species
shows that the magnitude of threats is
moderate and threats are ongoing, and
therefore, imminent. Therefore, we have
changed the listing priority number for
this plant variety from a 6 to a 9.
Dubautia imbricata ssp. imbricata
(Naenae)—This species is a shrub found
in wet forest and bogs on Kauai, Hawaii.
This subspecies is known from three
populations totaling 1,000 or more
individuals in the Wahiawa Mountains.
Threats to the species include pigs that
degrade and destroy habitat and
nonnative plants that outcompete and
displace it. We have changed the listing
priority number for this subspecies from
6 to 3 since the threats are ongoing, and
therefore, imminent.
Dubautia waialealae (Naenae)—This
species is a shrub found in bogs and
diverse mesic to wet forest on the Kauai,
Hawaii. This species is known from one
population totaling fewer than 800
individuals near the summit of
Waialeale and one individual at the
opposite end of the Alakai Plateau.
Threats to the species include pigs that
degrade and destroy habitat, and
nonnative plants that outcompete and
displace it. We have changed the listing
priority number for this species from 5
to 2 since the threats are ongoing, and
therefore, imminent.
Festuca hawaiiensis (no common
name)—This species is a cespitose
(grows in dense clumps) annual found
in dry forest on the islands of Hawaii
and Maui, Hawaii. This species is
known from more than 20 populations
totaling approximately 1,000
individuals in and around the
Pohakuloa Training Area on the island
of Hawaii. Historically, this species was
also found on Hualali and Puu
Huluhulu on Hawaii and possibly
Ulupalakua on Maui, but it no longer
occurs at these sites. The species is
threatened by pigs, goats, and sheep that
eat this plant and degrade, and destroy
habitat, by nonnative plants that
outcompete and displace it, and by fire
from military training. We have changed
the listing priority number for this
species from 5 to 2 since the threats are
ongoing, and therefore, imminent.
Gardenia remyi (Nanu)—This species
is a tree found in mesic to wet forest on
the islands of Kauai, Molokai, Maui, and
Hawaii, Hawaii. Gardenia remyi is
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known from several populations totaling
a few hundred individuals throughout
its range. The species is threatened by
pigs and goats that eat this plant and
degrade and destroy habitat, and by
nonnative plants that outcompete and
displace it. We have changed the listing
priority number for this species from 5
to 2 since the threats are ongoing, and
therefore, imminent.
Geranium hanaense (Nohoanu)—This
species is a decumbent (growing along
the ground) shrub found in bogs on
Maui, Hawaii. First described in 1988,
Geranium hanaense was known from
only two adjacent montane bogs on the
northeast outer rift of Haleakala, East
Maui. At that time the species was
represented by 500 to 700 individuals.
By 1996, the species population had
significantly declined according to State
biologists. Threats to the species include
pigs that degrade and destroy habitat,
and nonnative plants that outcompete
and displace it. We have changed the
listing priority number for this species
from 5 to 2 since the threats are ongoing,
and therefore, imminent.
Hazardia orcuttii (Orcutt’s
Hazardia)—Hazardia orcuttii is a
shrubby species in the Asteraceae
(sunflower family). Although once
described as fairly common in open
habitats along coastal plains from
Colonet to Tijuana in Baja California,
Mexico, only one occurrence has been
confirmed in Mexico since 1975. There
is only one known extant native
occurrence of this species in the United
States; it is in the Manchester
Conservation Area (MCA), managed by
the Center for Natural Lands
Management in the City of Encinitas.
Apparent threats to the species include
direct impacts from unauthorized access
and use of the MCA. Impacts include
pedestrian trespass, creation, and use of
bicycle trails, and use of the area for
unauthorized fire suppression methods
training. Introduced invasive exotic
plants may also pose a significant threat
to the species. Monitoring has not
recorded seedling recruitment at the
site. This species has a narrow
geographical range in the United States,
but the site is managed. Because this
species is State-listed and occurs in a
managed, protected area, the threats are
now nonimminent, but remain high in
magnitude. Therefore, we changed the
listing priority number for this species
from a 2 to a 5.
Hedyotis fluviatilis (Kamapuaa)—This
species is a scandent shrub found in
mesic to wet forest on Oahu and Kauai,
Hawaii. This species is known from six
populations totaling 500 to 1,000
individuals throughout its range. This
species is threatened by pigs that
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degrade and destroy habitat, and by
nonnative plants that outcompete and
displace it. We have changed the listing
priority number for this species from 5
to 2 since the threats are ongoing, and
therefore, imminent.
Indigofera mucronata var. keyensis
(Florida indigo)—This small, perennial
pea is found at edges of tropical
rockland hammock (forest), coastal
berm, and rock barren communities in
the upper Florida Keys (Monroe County,
Florida). Florida Keys indigo is
currently known only from Crawl Key
(private), Key Largo (John Pennekamp
Coral Reef State Park), Long Key State
Park, Long Point Key (private),
Plantation Key (private), and Windley
Key Fossil Coral Reef State Geological
Park. A population has been seen at
Snake Creek Hammocks, Florida Keys
Wildlife and Environmental Area,
managed by the Florida Fish and
Wildlife Conservation Commission.
This species appears to have been
extirpated from the Lower and Upper
Matecumbe Keys. Perhaps no more than
1,000 individuals exist. The coastal rock
barrens at two sites are being invaded by
native and exotic hardwoods, and the
exotic Brazilian pepper (Schinus
terebinthifolius) is a special concern as
the pepper is very competitive. For
example, on Long Point Key,
encroaching Brazilian pepper threatens
to close over the opening where a small
population of Florida indigo occurs. It is
unlikely this population will survive
another decade under current
conditions. The overall status of this
plant appears to be stable on public
conservation lands in the Keys due to
land acquisition by the State,
monitoring by the Florida Park Service,
and effective control of exotic pest
plants in some areas. Because the
threats to this plant are moderate and
are ongoing, and therefore, imminent,
we have changed the listing priority
number from 6 to 9.
Keysseria erici (no common name)—
This species is a short, rhizomatous
perennial herb found in montane bogs
on Kauai, Hawaii. Keysseria erici is
known from several populations in bogs
within the Alakai swamp region of
Kauai, totaling approximately 1,000
individuals. While the species has
always been restricted to the bogs of the
Alakai, it may have occurred in more
bogs in the area in the past. Threats to
the species include pigs that degrade
and destroy habitat, and nonnative
plants that outcompete and displace it.
We have changed the listing priority
number for this species from 5 to 2 since
the threats are ongoing, and therefore,
imminent.
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Keysseria helenae (no common
name)—This species is a rhizomatous
perennial herb found in montane bogs
on Kauai, Hawaii. Keysseria helenae is
known from three or four populations in
bogs within the Alakai swamp region of
Kauai, totaling approximately 300
individuals. While the species has
always been restricted to the bogs of the
Alakai, it may have occurred in more
bogs in the area in the past. Threats to
the species include pigs that degrade
and destroy habitat, and nonnative
plants that outcompete and displace it.
We have changed the listing priority
number for this species from 5 to 2 since
the threats are ongoing, and therefore,
imminent.
Korthalsella degeneri (Hulumoa)—
This species is a parasitic subshrub
found on two species of native trees,
Sapindus oahuensis and Nestigis
sandwicensis, only in diverse mesic
forests on Oahu, Hawaii. Recent surveys
indicate that the species is known only
from one population of 1,000
individuals in Makua Valley. Threats to
the species include goats that eat this
plant and degrade and destroy habitat,
by nonnative plants that outcompete
and displace it, and by fire. We have
changed the listing priority number for
this species from 5 to 2 since the threats
are ongoing, and therefore, imminent.
Labordia helleri (Kamakahala)—This
species is a shrub found in diverse
mesic forest and mesic valleys on Kauai,
Hawaii. This species is known from
eight or more populations totaling 500
individuals from Makaha to Honopu.
This species is threatened by goats and
deer that eat this plant and degrade and
destroy habitat, and by nonnative plants
that outcompete and displace it. We
have changed the listing priority
number for this species from 5 to 2 since
the threats are ongoing, and therefore,
imminent.
Labordia pumila (Kamakahala)—This
species is a sparingly branched shrub
found in hummocks in bogs and in bog
margins on Kauai, Hawaii. This species
is known from three populations
totaling 500 to 700 individuals in the
Alakai and Waialeale areas. This species
is threatened by pigs that eat this plant
and degrade and destroy habitat, and by
nonnative plants that outcompete and
displace it. We have changed the listing
priority number for this species from 5
to 2 since the threats are ongoing, and
therefore, imminent.
Lysimachia daphnoides (Lehua
makanoe)—This species is a small shrub
found in bogs on Kauai, Hawaii. This
species is known from nine populations
totaling 180 to 300 individuals in the
Alakai area. Threats to the species
include pigs and hikers that degrade
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and destroy habitat, and nonnative
plants that outcompete and displace it.
We have changed the listing priority
number for this species from 5 to 2 since
the threats are ongoing, and therefore,
imminent.
Melicope christophersenii (Alani)—
This species is a long-lived perennial
shrub or tree found in wet forest on
Oahu, Hawaii. Melicope
christophersenii was historically known
from the southern Waianae Mountains
on the island of Oahu. Currently, this
species is known from several
populations totaling less than 300
individuals. This species is threatened
by feral pigs and goats that eat this plant
and degrade habitat, competition from
nonnative plants, and predation by the
black twig borer. We have changed the
listing priority number for this species
from 5 to 2 since the threats are ongoing,
and therefore, imminent.
Melicope puberula (Alani)—This
species is a shrub or small tree found in
mesic and wet forest on Kauai, Hawaii.
This species is known from 1,000
individuals in the Kalalau area to
Wainiha Pali on the island of Kauai.
Threats to the species include feral pigs
and goats, nonnative plants, the black
twig borer, and naturally occurring
events. We have changed the listing
priority number for this species from 5
to 2 since the threats are ongoing, and
therefore, imminent.
Myrsine fosbergii (Kolea)—This
species is a branched shrub or small tree
found in cloudswept ridges and wet
forest on Kauai and Oahu, Hawaii. This
species is known from at least five
populations totaling 150 to 175
individuals from Kauai and the
southeastern end of Castle Trail on
Oahu. This species is threatened by feral
pigs and nonnative plants. We have
changed the listing priority number for
this species from 5 to 2 since the threats
are ongoing, and therefore, imminent.
Myrsine vaccinioides (Kolea)—This
species is a small branched shrub found
in shrubby bogs on Maui, Hawaii. This
species is found scattered throughout
the bogs of west Maui, totaling
approximately 500 individuals, but
regeneration is not occurring. This
species is found in the Puu Kukui area
of West Maui. Threats to the species
include feral pigs and nonnative plants.
We have changed the listing priority
number for this species from 5 to 2 since
the threats are ongoing, and therefore,
imminent.
Nothocestrum latifolium (Aiea)—This
species 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 approximately a dozen
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populations totaling less than 300
individuals. While the species has not
been extirpated from any island, its
range on each island has decreased
dramatically. Threats to the species
include feral pigs, goats and cattle,
nonnative plants, and the loss of
pollinators. We have changed the listing
priority number for this species from 5
to 2 since the threats are ongoing, and
therefore, imminent.
Penstemon debilis (Parachute
beardtoungue)—Penstemon debilis is
endemic to oil shale outcrops on the
Roan Plateau escarpment in Garfield
County, Colorado. The total estimated
number of plants is 450 to 750
individuals. Approximately 90 percent
of the plants are on private land owned
by Occidental Petroleum; the remaining
10 percent are on Bureau of Land
Management land that is proposed to be
open to leasing under a new Resource
Management Plan in 2005. Pressure to
develop energy reserves in this area is
intense. Threats also include habitat
destruction caused by road and
communication tower maintenance and
recreational use. A listing priority
number change from 5 to 2 is based on
a dramatic increase in the intensity of
energy exploration along the Roan
Plateau escarpment, making the threats
to the species imminent.
Phacelia submutica (DeBeque
phacelia)—Phacelia submutica is an
ephemeral annual flowering plant and is
endemic to clay soils derived from the
Atwell Gulch and Shire members of the
Wasatch Formation in Mesa and
Garfield Counties, Colorado. There are
about 40 populations; all are smaller
than 5 acres. The numbers of plants vary
from none to thousands each year,
depending on precipitation. The habitat
coincides with high quality oil and gas
reserves of the Piceance Basin, mostly
on Federal lands. The primary threats to
this species are gas field development
and associated construction and
transportation activities, as well as
increased access to all-terrain vehicles.
Substantial surface disturbance alters
the unique soil structure and destroys
seed banks that are crucial to the
survival of this species. We changed the
listing priority number from an 11 to an
8 primarily in response to a dramatic
increase in the intensity of energy
exploration and development on the
habitat, which make the low to
moderate threats imminent.
Phyllostegia floribunda (no common
name)—This species is an erect
subshrub found in mesic to wet forest
on the island of Hawaii, Hawaii. This
species is known from 4 populations
with a combined total of between 100 to
500 individuals in Laupahoehoe Natural
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Area Reserve and Hawaii Volcanoes
National Park. Threats to the species
include feral pigs, and nonnative plants.
We have changed the listing priority
number for this species from 5 to 2 since
the threats are ongoing, and therefore,
imminent.
Pittosporum napaliense (Hoawa)—
This species is a small tree found in
Pandanus forest and mesic valleys on
Kauai, Hawaii. This species is known
from about six populations, with a
combined total of several hundred
individuals on the eastern portion of the
Na Pali coast. Threats to the species
include feral pigs and nonnative plants.
We have changed the listing priority
number for this species from 5 to 2 since
the threats are ongoing, and therefore,
imminent.
Platydesma cornuta var. cornuta (no
common name)—This species is an
erect palmoid shrub found in mesic
forest on Oahu, Hawaii. This variety is
known from three to four populations,
with a combined total of approximately
100 individuals in the Koolau
Mountains on the island of Oahu.
Limited monitoring has shown that this
population is declining. Threats to the
species include feral pigs and nonnative
plants. We have changed the listing
priority number for this species from 5
to 2 since the threats are ongoing, and
therefore, imminent.
Platydesma cornuta var. decurrens
(no common name)—This species is an
erect palmoid shrub found in mesic
forest on Oahu, Hawaii. This variety is
known from a few populations, with a
combined total of a few hundred
individuals in the Waianae Mountains.
Threats to the species include feral pigs,
goats, and nonnative plants. We have
changed the listing priority number for
this variety from 6 to 3 since the threats
are ongoing, and therefore, imminent.
Platydesma rostrata (Pilo kea lau
lii)—This species is erect palmoid shrub
found in diverse mesic forest and
valleys on Kauai, Hawaii. This species
is known from about 20 populations
with a combined total of several
hundred individuals in Kokee and Kuia.
This species is threatened by feral goats
and nonnative plants. We have changed
the listing priority number for this
species from 5 to 2 since the threats are
ongoing, and therefore, imminent.
Pleomele fernaldii (Hala pepe)—This
species is a tree found in dry forest
habitat on Lanai, Hawaii, which has
become dramatically reduced due to
agriculture and habitat degradation.
Three populations of this species are
currently found on the island of Lanai
in the few remnant dry forests on the
leeward side of the island, with a
combined total of 200 individuals.
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Threats to the species include axis deer
and nonnative plants. We have changed
the listing priority number for this
species from 5 to 2 since the threats are
ongoing, and therefore, imminent.
Pleomele forbesii (Hala pepe)—This
species is a tree found in diverse mesic
and dry forests on Oahu, Hawaii.
Although previously thought to be more
common, this species is currently
known from 16 populations that have a
combined total of 500 individuals. This
species is threatened by feral pigs and
goats, nonnative plants, fire, and rats.
We have changed the listing priority
number for this species from 5 to 2 since
the threats are ongoing, and therefore,
imminent.
Pritchardia hardyi (Loulu)—This
species is a medium-sized palm tree
found in open wet forest on Kauai,
Hawaii. This species is known from
three populations with a combined total
of 300 individuals in the Power Line
Road area. This species is threatened by
feral pigs, rats, vandalism/collection,
and nonnative plants. We have changed
the listing priority number for this
species from 5 to 2 since the threats are
ongoing, and therefore, imminent.
Pseudognaphalium (=Gnaphalium)
sandwicensium var. molokaiense
(Enaena)—This species is a perennial
herb found in strand vegetation in dry
consolidated dunes on Molokai, Hawaii.
This variety is known from two
populations, one totaling a few hundred
individuals in the Moomomi area and
one population of 25 individuals on
west Maui at Puu Kahulianapa. Threats
to the species include predation by feral
deer, competition with nonnative
plants, collection by lei makers, and
destruction by off road vehicles. We
have changed the listing priority
number for this variety from 6 to 3 since
the threats are ongoing, and therefore,
imminent.
Pteralyxia macrocarpa (Kaulu)—This
species is a tree found in valleys and
slopes in diverse mesic forest on Oahu,
Hawaii. This species is known from 20
populations with a combined total of
less than 500 individuals. Threats to the
species include feral pigs, rats, the twospotted leafhopper, and nonnative
plants. We have changed the listing
priority number for this species from 5
to 2 since the threats are ongoing, and
therefore, imminent.
Ranunculus hawaiensis (Makou)—
This species is an erect or ascending
perennial herb found in mesic to wet
forest, dominated by Metrosideros
polymorpha (ohia) and Acacia koa (koa)
with scree substrate on Maui and the
island of Hawaii, Hawaii. Its range on
these two islands has declined.
Populations formerly within Haleakala
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National Park have been extirpated. It is
known from fewer than 300 individuals
in five populations. However, the
majority of these individuals are
seedlings, less than 1 inch (2.5
centimeters) tall. Species experts expect
the rate of survival to be very low due
to trampling by feral pigs, goats, cattle,
and sheep. Other threats to the species
include competition from nonnative
plants, and damage from slugs. We have
changed the listing priority number for
this species from 5 to 2 since the threats
are ongoing, and therefore, imminent.
Sicyos macrophyllus (Anunu)—This
species is a perennial vine found in wet
Metrosideros polymorpha (ohia) forest
and subalpine Sophora chrysophyllaMyoporum sandwicense (mamane/naio)
forest on the island of Hawaii, Hawaii.
This species is known from several
populations with a combined total of a
few hundred individuals in the Kohala
and Mauna Kea areas. This species is
threatened by feral pigs, sheep and
nonnative plants. We have changed the
listing priority number for this species
from 5 to 2 since the threats are ongoing,
and therefore, imminent.
Solanum nelsonii (Popolo)—This
species is a sprawling or trailing shrub
found in coral rubble or sand in coastal
sites on the islands of Hawaii, Molokai,
Maui, Niihau, Nihoa, Pearl, and Hermes,
Hawaii. This species is known from ten
populations with a combined total of
fewer than 300 individuals and is
declining rapidly on all islands,
including the Remote Islands National
Wildlife Refuge. In the past, this species
was also found on the islands of Oahu,
Kauai, Midway, and Laysan, but is
believed to be extirpated from these
locations, due primarily to coastal
development and competition with
nonnative plant species. This species is
threatened by nonnative plants,
development, off road vehicles, and
trampling. We have changed the listing
priority number for this species from 5
to 2 since the threats are ongoing, and
therefore, imminent.
Ferns and Allies
Christella boydiae (no common
name)—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; however, the species has been
extirpated from that location. This
species is known from three populations
with a combined total of 362 to 412
individuals. The three populations are
found in Kipahulu Valley and Waihoi
Valley of Maui and the Koolau
Mountains of Oahu. Current
populations survive only at the extreme
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upper elevations of streambanks. This
species is threatened by feral ungulates,
nonnative plants, stream diversion, and
erosion. We have changed the listing
priority number for this species from 5
to 2 since the threats are ongoing, and
therefore, imminent.
Microlepia strigosa var. mauiensis
(Palapalai)—This fern is found in mesic
to wet forests. The species was
historically found on the islands of
Maui and Hawaii, Hawaii, but is
currently found only on the island of
Maui, where it is known from three
populations with a combined total of
100 to 200 individuals. This species is
threatened by feral pigs that eat this
plant and degrade and/or destroy
habitat, by nonnative plants that
compete for light and nutrients, and
reduce this species’ vigor; and by
stochastic extinction due to naturally
occurring events. We have changed the
listing priority number for this species
from 2 to 3 because this entity is now
recognized as a variety of another
species. The threats to this variety
remain imminent and of a high
magnitude.
Keysseria helenae. Also, see above in
‘‘Summary of Listing Priority Changes in
Candidates.’’
Ferns and Allies
Christella boydiae (D.C.Eaton)
Holttum—This species has no common
name and is in the family
Thelypteridaceae. Christella boydiae
was originally described as Aspidium
boydiae by D.C. Eaton in 1897, and in
previous CNORs we showed A. boydiae
as a candidate. The currently recognized
Latin name, Christella boydiae, was
published by R.E. Holttum in 1966. This
name is accepted by a recent treatment
of the fern flora of Hawaii (Palmer
2003). Thus, with this current CNOR
and accompanying species assessment
form, we are recognizing the candidate
entity as Christella boydiae. Also, see
above in ‘‘Summary of Listing Priority
Changes in Candidates.’’
Huperzia stemmermanniae (A.C.
Medeiros & W.H. Wagner) Kartesz—This
species has no common name but is a
type of hanging firmoss in the
Lycopodiaceae (Club-moss family).
Huperzia stemmermanniae was
originally described as Phlegmariurus
Other Taxonomic Changes in
stemmermanniae by A.C. Medeiros and
Candidates
W.H. Wagner (Medeiros et al. 1996)
based on specimens collected on
Flowering Plants
Haleakala, Maui, Hawaii, by Medeiros
Keysseria erici (C.N. Forbes) Cabrera— and Chimera in 1995. The currently
This species has no common name and
recognized Latin name, Huperzia
is in the Asteraceae (Sunflower family).
stemmermanniae, was published in
Keysseria erici was originally described
1999 (Kartez 1999). This name is
as Lagenophora erici by C.N. Forbes in
accepted by a recent treatment of the
1918. The currently recognized Latin
fern flora of Hawaii (Palmer 2003).
name, Keysseria erici, was published by Thus, with this current CNOR and
Cabrera in 1967. This name is accepted
accompanying species assessment form,
in the 2003 supplement to the Manual
we are recognizing the candidate entity
of the Flowering Plants of Hawaii
as Huperzia stemmermanniae (rather
(Wagner and Herbst 2003). Thus, with
than the name we previously used,
this current CNOR and accompanying
Phlegmariurus stemmermanniae).
species assessment form, we recognize
Huperzia stemmermanniae is found in
the candidate entity as Keysseria erici
mesic Metrosideros polymorpha (ohia)/
(rather than the name we previously
Acacia koa (koa) forests on the islands
used, Lagenophora erici). Also, see
of Maui and Hawaii, Hawaii. This
above in ‘‘Summary of Listing Priority
species was historically known only
Changes in Candidates.’’
from east Maui. Additional populations
Keysseria helenae (C.N. Forbes &
are found in Laupahoehoe on the island
Lydgate) Cabrera—This species has no
of Hawaii. Only four populations are
common name and is in the Asteraceae
known, totaling less than 20 individuals
(Sunflower family). Keysseria helenae
on Hawaii and Maui. This species is
was originally described as
threatened by feral pigs, goats, and
Lagenophora helenae by C.N. Forbes
cattle, which eat this plant and degrade
and J. Lydgate in 1918, and in previous
and/or destroy habitat; fire that also
CNORs we showed L. helenae as a
destroys habitat and plants; and,
candidate. The currently recognized
nonnative plants that outcompete it for
Latin name, Keysseria helenae, was
light and nutrients. Because the threats
published by Cabrera. This name is
are of a high magnitude and are
accepted in the 2003 supplement to the
imminent, we are continuing to assign
Manual of the Flowering Plants of
this species a listing priority number of
Hawaii (Wagner and Herbst 2003). Thus, 2.
Microlepia strigosa var. mauiensis
with this current CNOR and
accompanying species assessment form, (palapalai) is in the family
Dennstaedtiaceae. Microlepia strigosa
we recognize the candidate entity as
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var. mauiensis was originally described
as Microlepia mauiensis by W.H.
Wagner and in previous CNORs we
showed M. mauiensis as a candidate.
The currently recognized Latin name,
Microlepia strigosa var. mauiensis, was
published by D. Palmer in 2002. This
name is accepted in his recent treatment
of the fern flora of Hawaii Palmer
(2003). Also, see above in ‘‘Summary of
Listing Priority Changes in Candidates.’’
Candidate Removals
Clams
Alabama clubshell (Pleurobema
troshelianum) and painted clubshell
(Pleurobema chattanoogaense)—Based
on recent genetic and morphological
studies by Williams et al. and Campbell
(see the species assessment forms for
references and details), these two taxa
are no longer considered valid, and do
not meet the Act’s definition of a
species. Therefore, we are removing
both species from candidate status.
Insects
Holsinger’s Cave beetle
(Pseudamophthalmus holsingeri)—
Holsinger’s cave beetle is a cavedependent predatory ground beetle
found in a single cave, Young-Fugate
Cave, located in Lee County, Virginia.
Through conservation efforts, two
previous major threats have been
eliminated: (1) A highway widening
project proposed to be constructed near
the cave has been modified to avoid
impacts to the cave, and, (2) a leaking
underground fuel tank from a gas station
located over the cave has been removed.
Additionally, the cave entrance is
located on private land where the
landowners strictly prohibit entry into
the cave. Although water entering
Young-Fugate cave is somewhat affected
by sources of non-point source
pollution, results of monitoring the cave
beetle population have shown no
evidence that current surrounding land
use has negatively impacted the cave
beetle. Thus, threats to this species have
been eliminated and the species no
longer meets the definition of a
candidate species.
Crustaceans
Camp Shelby burrowing crayfish
(Fallicambarus gordoni)—The Camp
Shelby burrowing crayfish (CSBC) is
found in pitcher plant wetlands of
southern Mississippi. CSBC has a small,
naturally limited range in a localized
portion of the Leaf River watershed in
central Perry County, Mississippi,
within the Desoto National Forest. All of
this area is currently under lease to the
Mississippi Army National Guard’s
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Camp Shelby for troop and tank training
grounds. A Candidate Conservation
Agreement (CCA) was developed and is
being implemented by the Mississippi
Army National Guard, U.S. Forest
Service, Mississippi Department of
Wildlife, Fisheries and Parks, and the
Service. This CCA addresses all threats
known to the species (silviculture, troop
and tank maneuvers, and ATV use) and
implements an aggressive habitat
management and monitoring program.
This signed CCA has removed threats to
the CSBC and its habitat to the point
that the species no longer meets the
criteria for candidate status. We are
removing this species from the
candidate list primarily as a result of the
conservation efforts outlined in the
CCA.
Petition Findings for Candidate Species
The Act provides two mechanisms for
considering species for listing. One
method allows the Secretary, on her
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 that (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 but
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precluded finding on a petition, we are
to treat such a petition as one that is
resubmitted on the date of such a
finding. Thus, we 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,
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 12month finding to the candidate list.
This publication also 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
finding, we reviewed the status of the
newly petitioned candidate species and
through this CNOR are publishing
specific section 4(b)(3) findings (i.e.,
substantial 90-day and warranted-butprecluded 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 12month petition finding in compliance
with section 4(b)(3)(B) of the Act at least
once a year, until we publish a proposal
to list the species or make a final notwarranted finding. We make this annual
finding 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
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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 annually a
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
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 also 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 12month 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
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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 S–
03–1758 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
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.
We have drafted this CNOR to address
the concerns of these courts. 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 listing priority number 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 candidate species.
Pursuant to section 4(b)(3)(C)(ii) and
the Administrative Procedure Act (5
U.S.C. 206), any party with standing
may challenge the merits of any notwarranted or warranted-but-precluded
petition finding incorporated in this
CNOR. The analysis included herein,
together with the administrative record
for the decision at issue (particularly the
supporting species assessment form),
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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 one year of
the date of publication of this CNOR. If
we fail to make any such finding on a
timely basis, whether through
publication of a new CNOR or some
other form of notice, any party with
standing may seek judicial review.
In this CNOR, we are addressing the
concerns of the courts by adding more
specific information into our discussion
on preclusion (see below). In preparing
this CNOR, we reviewed the current
status of and threats to the 262
candidates and 5 listed species for
which we have received a petition and
for which we have found listing or
reclassification from threatened to
endangered to be warranted-butprecluded. 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. This is the first
12-month petition finding for those
candidate species that were petitioned
since the last CNOR (225 species), as
well as for one new candidate species,
the Miami blue butterfly, that was
petitioned prior to this CNOR but for
which we have not already published a
separate warranted-but-precluded 12month finding (we have previously
published a separate substantial 90-day
petition finding for this 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 (for the
Columbian Basin DPS of the greater
sage-grouse, see below). 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 12month 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. As
discussed above, 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
April 19, 2004, through May 2, 2005.
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We will continue to monitor the status
of all candidate species, including
petitioned species, as new information
becomes available. This review will
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 Web site: 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
of species determined to be threatened
species or endangered species pursuant
to the Act. Below we describe the
actions that continue to preclude the
immediate proposal of a regulation and
final promulgation of a regulation
implementing the petitioned action, 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 a species’
listing priority in relation to the
resources that are available and
competing demands for those resources.
(As described above in the Summary,
the listing priority of a species is
represented by the listing priority
number we assign to it.) 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 appropriations process, and we
cannot spend more than is appropriated
for the Listing Program without
violating the Anti-Deficiency Act. The
number of listing actions that we can
undertake in a given year also is
influenced by the complexity of those
listing actions, i.e., more complex
actions generally are more costly. For
example, for FY 2002 to FY 2004, the
costs (excluding publication costs) for
conducting a 12-month finding, without
a proposed rule, ranged from
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approximately $9,600 for one species
with a restricted range and involving a
relatively uncomplicated analysis, to
$305,000 for another species that was
wide-ranging and involved a complex
analysis.
In FY 1998 and for each fiscal year
since then, Congress placed a statutory
cap on funds which may be expended
for listing and critical habitat actions
(i.e., 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 ESA functions, or for other
Service programs, from being used for
listing or critical habitat actions (see
House Report 105–163, 105th Congress,
1st Session).
Beginning in FY 2002, Congress also
put in place the critical habitat
‘‘subcap,’’ which put an upper limit on
the Listing Program funds that could be
spent on work related to critical habitat
designations for already listed species.
Recognizing that designation of critical
habitat for species already listed would
consume most of the overall Listing
Program appropriation, Congress put the
subcap in place to ensure that some
funds would be available to make other
listing determinations: ‘‘The critical
habitat designation subcap will ensure
that some funding is available to
address other listing activities’’ (H.R.
Rep. No. 103, 107th Cong., 1st Sess.
2001 at 30, 2001 WL 695998). Because
the Service has had to use virtually the
entire critical habitat subcap to address
court-mandated designations of critical
habitat, Congress in effect determined,
through the listing cap and the critical
habitat subcap, the amount available for
other listing activities. It is this amount
(i.e., the funds in the listing cap other
than those covered by the critical
habitat subcap) that is used in the
determination here of preclusion and
expeditious progress.
Congress also has recognized that the
availability of resources was the key
element in deciding whether we would
issue a listing proposal or make a
‘‘warranted but precluded’’ finding for a
given species. The Conference Report
accompanying Public Law 97–304,
which established the current statutory
deadlines and the warranted-butprecluded finding, states (in a
discussion on 90-day petition findings
that by its own terms also covers 12month 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
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[i.e. for a lower-ranking species]
unwise.’’ Therefore, in fiscal year 2004,
the outer parameter within which
‘‘expeditious progress’’ must be
measured is that amount of progress that
could be achieved by spending $3.38
million, which was the amount
available in the Listing Program
appropriation not within the critical
habitat subcap (i.e., all funds within the
critical habitat subcap were used to
comply with court orders or courtapproved settlement agreements, and
thus were not available for other listing
activities).
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. However, through
court orders and court-approved
settlements, federal district courts have
mandated that we must complete
certain listing activities with respect to
specified species and have established
the schedules by which we must
complete those activities. The species
involved in these court-mandated listing
activities are not always those that we
have identified as being most in need of
listing. A large majority of the
appropriation available for new listings
of species (of the $3.38 million) was
consumed by such court-mandated
listing activities in FY 2004, and by
ordering or sanctioning these actions the
courts essentially determined that these
were the highest priority actions to be
undertaken with available funding.
Accordingly, in FY 2004, FWS had little
discretion to determine what listing
activities to undertake and what species
to address. Copies of all of the court
orders and settlement agreements
referred to below are available from the
Service and are part of the
administrative record for these
resubmitted petition findings.
On November 10, 2003, the President
signed the 2004 Interior and Related
Agencies Appropriations Act (Pub. L.
108–108), which, as a result of the
subcap, in effect included $3,386,000
for listing activities not related to
critical habitat designations for species
that already are listed. This
appropriation was fully allocated to
fund the following categories of actions
in the Listing Program: emergency
listings; essential litigation-related,
administrative and program
management functions; compliance
with court orders and court-approved
settlement agreements requiring that
petition findings or listing
determinations be completed by a
specific date; section 4 listing actions
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with absolute statutory deadlines; and
high-priority listing actions. Based on
the available funds and their allocation
for these purposes, no FY 2004 funds
were available for listing actions for any
of the candidate species included in
Table 1 of this notice, except for some
funds that were used for work on the
Southwest Alaska population of the
northern sea otter, boreal toad, and salt
creek tiger beetle. Specific details
regarding the individual actions taken
using the FY 2004 funding, which
precluded our ability to undertake
listing proposals for any of the
candidate species, except these three
species noted above, are provided
below.
We note here that the category of
‘‘high-priority listing actions’’
mentioned above refers to actions for
which no timeline has been established
by a court order or settlement
agreement, and that also are not subject
to an absolute statutory deadline. Our
ability to work on such listing actions is
quite limited. In recent years, our
allocation of Listing Program funds has
included a limited amount of funding
($100,000) to each Regional office to
ensure that the office maintains minimal
core capacity for listing actions (e.g.,
evaluating the status of species to help
ensure that emergency listing action can
be taken if necessary, participating in
work to meet the statutory requirement
to annually review and make findings
on resubmitted petitions). In a Region
that faces a relatively limited workload
in the Listing Program with regard to
deadlines resulting from court orders or
settlement agreements, and a relatively
limited workload related to meeting
statutory deadlines, some of this
‘‘capability’’ funding may be available to
address high priority listing actions.
However, in most Regions the limited
amount of capability funding for
Regional offices included in an
allocation is used for work associated
with supporting listing actions related
to court orders or settlement
agreements, and for meeting statutory
deadlines (i.e., there are no funds
available for high priority listing
actions).
The overall Listing Program situation
in FY 2005 is similar to that in FY 2004.
For FY 2005, Congress appropriated
$4,043,000 to the listing program that
cannot be spent on critical habitat for
already listed species (Pub.L. 108–447,
signed on December 8, 2004). We have
recently prepared the allocation of this
appropriation. The $4,043,000 is fully
allocated to fund the following listing
actions: any emergency listings;
essential litigation-related,
administrative, and program
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management functions; compliance
with court orders or court-approved
settlement agreements requiring petition
findings or listing determinations; and
high-priority listing actions. While
being similar to FY 2004, the Listing
Program situation for FY 2005 is
different in that we estimate that we
have approximately $1.7 million from
the critical habitat subcap that is not
needed, at this time, to fund critical
habitat designations that are the subject
of court order or court-approved
settlement agreements. We are currently
working on allocating this money to our
Regions for work on statutorily-required
petition findings and potential work on
proposed listing determinations for
some high-priority candidate species.
During the current fiscal year, we will
issue proposed listing rules for the
highest priority candidate species only
if doing so does not jeopardize our
ability to comply with court orders,
court-approved settlement agreements,
or unqualified statutory deadlines.
Consequently, as of the date of the
publication of this CNOR, we anticipate
that we will have only limited FY 2005
funds available to work on proposals to
list any of the candidate species
included in Table 1 (with the exception
of the Salt Creek tiger beetle which is
work that was done per a courtapproved settlement agreement and the
Gunnison sage-grouse, which is a high
priority listing action, as explained
below), and consequently we continue
to find that proposals to list these
species are warranted but precluded.
We note also that all of the actions that
demonstrate our expeditious progress
on listing that we have completed to
date or will complete in FY 2005 (see
below) contribute to the preclusion of
work on listing proposals for these
candidate species.
In addition to being precluded by lack
of available funds, work on proposed
rules for candidates with lower priority
(i.e., those that have listing priority
numbers of 4–12) is also precluded by
the need to issue proposed rules for
higher priority species facing highmagnitude, imminent threats (i.e.,
listing priority numbers of 1–3). Table 1
shows the listing priority number for
each candidate species. Finally, 12month ‘‘warranted but precluded’’
petition findings for reclassification of
threatened species to endangered are
lower priority, since the listing of the
species already affords the protection of
the Act and implementing regulations.
As explained above, part of the basis
for making a warranted-but-precluded
finding is that expeditious progress is
being made to add qualified species to
the Lists. Our progress in FY 2004
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includes work in the following
categories: (1) Evaluation of the
potential need for emergency listing of
1 species; (2) preparation and
publication of final listing
determinations involving 10 species; (3)
preparation and publication of a
proposed listing action for 1 species; (4)
preparation of proposed or final listing
actions (not yet completed so not yet
published) for 6 species; (5) and petition
findings for 55 species (11 completed
findings; 40 resubmitted; 4 findings not
yet completed). Specific information
regarding each of these categories for FY
2004 is provided below.
(1) Emergency listings—We worked
on a proposed rule to list the Miami
blue butterfly. The Miami blue butterfly
is restricted to one isolated population
on Bahia Honda Key in Florida and is
threatened by the combined influences
of catastrophic environmental events,
habitat destruction or modification,
mosquito control activities, potential
illegal collection, potential loss of
genetic heterogeneity, and potential
predation. Work on assessing the status
of the species and preparing a listing
rule originally was approved for funding
and was initiated in FY 2004 because at
the time, the Region considered that it
was an emergency. We later decided not
to exercise our discretion under section
4(b)(7) to emergency list the species
(based in part on the existence of a
captive-bred population). However,
because a review of the species had
been conducted and the emergency rule
already was drafted, and because it was
a high priority species, continued work
on the proposed listing was approved.
Recently, however, we decided that the
limited funds that were available to
work on a proposed rule for this species
should instead be used to work on
higher priority candidate species (i.e.,
species with a LPN of 2). Therefore,
rather than completing and issuing a
proposed rule to list this species, we are
including it in the CNOR as a new
candidate.
(2) Final listing determinations—We
prepared and published in the Federal
Register final listing determinations for
ten species, all of which had deadlines
mandated by court orders or courtapproved settlement agreements, in
addition to the absolute statutory
deadline imposed by section 4(b)(6).
These included final regulations listing
eight species and final decisions to
withdraw the proposed listing rules for
two species. The eight species we listed
were: Rota bridled white-eye (69 FR
3022; January 22, 2004; LPN = 2), Santa
Catalina Island fox, Santa Rosa Island
fox, San Miguel Island fox, and Santa
Cruz Island fox (69 FR 10335 for all four
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fox subspecies; March 5, 2004; LPN = 3);
two plant species (Nesogenes rotensis
and Osmoxylon mariannense) from the
Commonwealth of the Northern Mariana
Islands (69 FR 18499; April 8, 2004;
LPN = 1 and 2, respectively); and the
California tiger salamander (69 FR
47211; August 4, 2004; LPN = 3). (We
note that the work on the salamander
included funding for the designation of
critical habitat for the central California
distinct population segment (DPS). The
critical habitat subcap pertains to
critical habitat designations for species
already listed; we may use listing funds
for critical habitat designation work
conducted in conjunction with a listing
action, as was the case with this DPS.
This work was necessary to comply
with the Act’s deadline for designating
critical habitat: concurrent with listing
or within one year thereafter if
concurrent designation is not
determinable). The two species for
which we withdrew proposed listing
rules were: the slickspot peppergrass (69
FR 3094; January 22, 2004; previously
LPN = 2); and Tabernaemontana
rotensis (a plant species with LPN = 2);
the decision to not list this species was
included as part of the Federal Register
publication of the final rules listing the
two plant species from the
Commonwealth of the Northern Mariana
Islands, mentioned above (69 FR 18499).
(3) We prepared and published a
proposed regulation to list the
southwest Alaska distinct population
segment of the northern sea otter, which
has an LPN = 3 (69 FR 6600; February
11, 2004)). This DPS occurs in nearshore
locations from Attu Island in the west
to Kamishak Bay in the east, including
waters along the Aleutian Islands, the
Alaska Peninsula, and the Kodiak
archipelago. Although its range has not
been curtailed, this population has
declined by 56–68 percent since the
mid-1980’s and the decline shows no
evidence of abating (see proposed rule
for additional information). This
proposal was not the result of a deadline
established by a court order or a courtapproved settlement agreement. Rather,
this was the highest priority listing
action for the Alaska Region. (Initially
we determined that the Aleutian Islands
DPS of the northern sea otter was a
candidate with LPN = 3 (66 FR 54807),
and subsequently determined that the
DPS encompasses southwest Alaska.)
The Alaska Region generally has not
faced the relatively heavy Listing
Program workload experienced by
several other Regions, and consequently
was able to use their limited Regional
office capability funding in FY 2004 to
support the completion of this proposed
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listing regulation. We could not have
utilized this capability funding to
complete listing actions in other
Regions without eliminating the ability
of this Region to monitor the status of
candidate species and address any
emergency situations that might arise.
(4) We funded work on proposed or
final listing actions for 6 species for
which work was not completed in FY
2004. This included work on final
listing actions for the Sacramento
Mountains checkerspot butterfly, the
Mariana fruit bat (LPN = 3), and the
southwest Alaska DPS of the northern
sea otter (LPN = 3). It also included
work on proposed listing actions for the
boreal toad (LPN = 3), Salt Creek tiger
beetle (LPN = 3), and Miami blue
butterfly. The work on all these species,
except on the northern sea otter (see (3)
above) and Miami blue butterfly (see (1)
above), was in response to a court order
or a court-approved settlement
agreement, and all of the final listing
determinations are subject to absolute
statutory deadlines under section
4(b)(6).
(5) We funded work on 55 petition
findings. This involved 90-day findings,
initial 12-month findings, and findings
on resubmitted petitions. As explained
below, in some instances, the work has
been based on meeting deadlines
established by court order or by
settlement agreements. In other
instances, the work has been done in
order to meet statutory deadlines. All
12-month findings are subject to an
unqualified statutory deadline. With
regard to 90-day findings, the decision
in Biodiversity Legal Foundation v.
Badgley, 309 F. 3d 1166 (9th Cir. 2002),
held that the Act requires that 90-day
petition findings (i.e., the initial finding
as to whether a petition contains
substantial information, which the Act
directs us to make within 90 days of
receipt of a petition, if practicable) must
be made no later than 12 months after
receipt of the petition, regardless of
whether it is practicable to do so. Thus,
all 90-day findings are arguably subject
to an absolute statutory deadline. As a
result of this ruling, which changed our
interpretation of section 4(b)(3) of the
Act, we have been working to issue
petition findings on most of the
outstanding petitions for those species
that we have not previously determined
to warrant candidate status.
Some petition findings are
‘‘complete’’ actions. This includes 12month petition findings in which we
determine that listing was not warranted
and 90-day petition findings in which
we determine that the petition did not
present substantial information. In these
cases, our listing work is complete.
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24889
In FY 2004, we funded work on and
published 11 petition findings for the
following species: wolverine (notsubstantial 90-day finding) (68 FR
60112; October 21, 2003); eastern
subspecies of the greater sage-grouse
(not-substantial 90-day finding) (69 FR
933; January 7, 2004); Midvalley fairy
shrimp (not-warranted 12-month
finding) (69 FR 3592; January 26, 2004);
Cymopterus deserticola (desert
cymopterus—substantial 90-day
finding) (69 FR 6240; February 10,
2004); fisher (West coast DPS)
(warranted-but-precluded 12-month
finding) (69 FR 18769; April 8, 2004);
Florida black bear (partial remand of
not-warranted 12-month finding) (69 FR
2100; January 14, 2004); greater sagegrouse (substantial 90-day finding) (69
FR 21484; April 21, 2004); Colorado
river cutthroat trout (not-substantial 90day finding) (69 FR 21151; April 20,
2004); New England cottontail
(substantial 90-day finding) (69 FR
39395; June 30, 2004), black-tailed
prairie dog (not-warranted 12-month
resubmitted petition finding) (69 FR
51217; August 18, 2004); and, western
gray squirrel (not substantial 90-day
finding) (69 FR 58115). All 12-month
findings have absolute statutory
deadlines. Because of Badgley, all 90day findings arguably also have absolute
statutory deadlines. In addition, the
work on all these species, with the
following exceptions, was in response to
court orders or court-approved
settlement agreements. The New
England cottontail was the highest
priority listing action for the Northeast
Region. The Northeast Region generally
has not faced the relatively heavy
Listing Program workload experienced
by several other Regions, and
consequently was able to use their
limited Regional office capability
funding in FY 2004 to support the
completion of this petition finding. We
could not have utilized this capability
funding to complete listing actions in
other Regions without eliminating the
ability of this Region to monitor the
status of candidate species and address
any emergency situations that might
arise. Work on the greater sage-grouse
was a high priority action since we were
already working on sage-grouse issues
related to the court-ordered petition
finding for the eastern sage-grouse. In
our 90-day finding for the eastern sagegrouse, we committed to respond to the
listing petitions for the greater sagegrouse within 90 days, and to make a
12-month finding within 12 months, if
required. Having made this public
commitment, and given the history of
litigation involving various populations
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of sage-grouse, we accorded the same
priority to these petition findings as we
would to a court-ordered petition
finding. Work on the black-tailed prairie
dog was a high priority listing action;
we had previously funded much of the
work on this species in 2000 when we
made the initial 12-month warrantedbut-precluded petition finding and in
2001–2003 when we made resubmitted
petition findings that listing was still
warranted but precluded. The
Mountain-Prairie Region was able to use
some of their capability funds from FY
2004 to make the not-warranted petition
finding for the black-tailed prairie dog.
The allocated funds also supported
work on petition findings that were not
completed in FY 2004, which involved
work on findings for the following 4
species: white-tailed prairie dog (90-day
finding), greater sage-grouse (12-month
finding), Bromus arizonicus (Arizona
brome ‘‘90-day finding), and Nassella
cernua (nodding needlegrass—90-day
finding). Work on the white-tailed
prairie dog was in response to a court
order, while the work on the sage-grouse
was a high priority listing action with a
statutory deadline (see above). Work on
the statutorily-required petition findings
for Arizona brome and nodding
needlegrass was done using a small
amount of capability funds that was left
at the end of the fiscal year; this was a
high priority for the Pacific Region.
In addition, we completed
resubmitted petition findings required
by statute for 40 petitioned species that
are candidates. We published these
findings on May 4, 2004, as part of the
previous Candidate Notice of Review
(CNOR) (69 FR 24876). Since we had
identified many of these species as
candidates prior to receiving a petition
to list them, we had already assessed
their status using funds from our
Candidate Conservation Program (a
separate budget item within the
Endangered Species Program).
Our anticipated progress in FY 2005
includes work in the following
categories: (1) Preparation and
publication of final listing actions for 9
species; (2) initial work toward
preparation and publication of proposed
listing actions for 4 species; (3) and
work on petition findings for 17 species
that are not candidate species, initial
petition findings for 225 candidate
species that were petitioned since the
last CNOR, and resubmitted petition
findings for 37 candidate species that
were petitioned prior to the last CNOR.
Specific information regarding each of
these categories for FY 2005 is provided
below. We note also that Regions will
continue to monitor the status of
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candidates and prepare emergency
listing packages as needed.
(1) We are funding work on the final
listing determinations for the following
species: Mariana fruit bat (final listing
rule was published on January 6, 2005
(70 FR 1190)), southwest Alaska DPS of
the northern sea otter, Gila chub, Salt
Creek tiger beetle, Sacramento
Mountains checkerspot butterfly
(withdrawal of the proposed rule was
published on December 21, 2004 (69 FR
76428)), and four Southwestern
invertebrates (Koster’s tryonia snail,
Pecos assiminea snail, Roswell
springsnail, and Noel’s amphipod). All
of these final listing determinations are
responding to court orders or courtapproved settlement agreements, with
the exception of the work on the final
listing determination for the southwest
Alaska DPS of the northern sea otter (see
above for explanation on why this work
was funded). Now that the sea otter is
proposed for listing, a final listing
determination is subject to an absolute
statutory deadline.
(2) We are funding proposed listing
determinations for the boreal toad and
the Salt Creek tiger beetle, and a
remanded final listing determination for
the cactus ferruginous pygmy owl,
pursuant to court-approved settlement
agreements and a court order. The
proposed listing rule for the Salt Creek
tiger beetle was published on February
1, 2005 (70 FR 5101). The work on a
proposed listing determination for the
boreal toad has not been completed and,
thus, we are making a resubmitted
petition finding for this species within
this CNOR. Additionally, we are
funding a proposed listing
determination for the Gunnison sagegrouse, which is a high priority listing
action (LPN = 2) and the subject of
litigation.
(3) We also are funding work on
petition findings for the following
species: white-tailed prairie dog (notsubstantial 90-day finding published on
November 9, 2004 (69 FR 64889)),
Queen Charlotte goshawk (remanded
not-warranted 12-month finding),
pygmy rabbit (rangewide 90-day and 12month findings), greater sage-grouse
(entire range) (12-month not-warranted
finding published January 12, 2005 (70
FR 2273)), California spotted owl (90day finding), Yellowstone cutthroat
trout (12-month finding), Cicurina
cueva (cave spider—90-day and 12month findings) (substantial 90-day
finding published on February 1, 2005
(70 FR 5123)), four species of Pacific
lamprey (not-substantial 90-day findings
published on December 27, 2004 (69 FR
77152 and 69 FR 77158)), three species
of springsnail (substantial 90-day
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finding published on April 20, 2005 (70
FR 20512)) (Cymopterus deserticola
(desert cymopterus—12-month finding),
Dalea tentaculoides (Gentry’s
indigobush ‘‘90-day and 12-month
findings) (substantial 90-day finding
published on February 2, 2005 (70 FR
5401)), Ptilagrostis porteri (porter
feathergrass) (not-substantial 90-day
finding published on February 4, 2005
(70 FR 5959)). The work on all of the
above species is pursuant to court
orders or court-approved settlement
agreements, except for work on the
greater sage-grouse (see 5) above under
FY 2004 work) and the California
spotted owl, which is being done in
relation to ligtigation. We also funded
work on initial petitions findings for
225 candidate species (species
petitioned after the last CNOR) and
resubmitted petition findings for 37
petitioned candidate species (species
petitioned prior to the last CNOR). As
explained above, these initial and
resubmitted petition findings are
required by statute and findings for 261
of them are being published as part of
this CNOR (the resubmitted petition
finding for the Columbia Basin DPS of
the greater sage-grouse will be
completed later, as we have new
information that needs to be evaluated).
We are also funding work on the next
annual review of those resubmitted
petition findings which will be
published as part of the next CNOR.
Because the majority of these species
were already candidate species prior to
our receipt of a petition to list them, we
had already assessed their status using
funds from our Candidate Conservation
Program. We also continue to monitor
the status of these species through our
Candidate Conservation Program. The
cost of updating the species assessment
forms and publishing the joint
publication of the CNOR and
resubmitted petition findings is shared
between the Listing Program and the
Candidate Conservation Program.
As with our ‘‘precluded’’ finding,
‘‘expeditious progress’’ is a function of
the resources that are available and the
competing demands for those funds. As
discussed above, the funds in the
Listing Program that would be otherwise
available for adding other qualified
species to the Lists in FY 2004 and FY
2005 have been spent or must be spent
on complying with court orders and
court-approved settlement agreements
to make petition findings, court orders
and court-approved settlement
agreements to make final listing
determinations for other species,
meeting statutory deadlines for petition
findings or listing determinations, a few
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high-priority Service-initiated listing
determinations, essential litigation
support, and administrative and
management tasks.
Because virtually all of the money to
add qualified species to the list is
consumed in complying with court
orders or court-approved settlement
agreements requiring petition findings
or listing determinations, and essential
litigation-related, administrative, and
program management functions related
to these findings and determinations,
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, these
actions described above collectively
constitute expeditious progress.
Findings for Petitioned Candidate
Species
Mammals
Pacific Sheath-tailed Bat
(Emballonura semicaudata
semicaudata)—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 Pacific sheath-tailed
bat was once common and widespread
in Polynesia and Micronesia and is the
only insectivorous bat recorded from a
large part of this area. Historically, the
Pacific Sheath-tailed bat occurred in
American and Independent Samoa,
Guam, Commonwealth of the Northern
Mariana Islands (CNMI), Caroline
Islands, Tonga, Fiji, and Vanuatu. Four
subspecies are recognized: E. s. rotensis,
endemic to the Mariana Islands; E. s.
sulcata, occurring in Chuuk and
Pohnpei; E. s. palauensis, found in
Palau; and E. s. semicaudata, occurring
in American and Independent Samoa,
Tonga, Fiji, and Vanuatu.
The primary threats to the species as
a whole include the loss of roosting
caves (through various means), the loss
of foraging habitat due to deforestation,
disturbance by feral ungulates, natural
disasters, and possibly pesticide use in
the Mariana Islands. Disturbances to
caves and burning of forests have
contributed to the decline of bats in Fiji.
These threats are occurring already,
have been occurring for several decades,
and are affecting a large proportion of
the population.
This subspecies on American Samoa
declined from around 11,000 bats in
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1982 to only 200 in 1998. Since that
time, few bats have been observed;
however, the reasons for the decline of
the subspecies are unclear. Two caves at
Anapeapea Cove were reported as
roosting sites for most of the bats
estimated in 1976 and 1977. Both caves
were severely damaged during several
typhoons between 1987 and 1992, and
no bats were reported in either cave
during 1993 surveys. Only small
numbers of bats have been observed in
other caves during past surveys, but
there is no information on how many
other caves exist or how many bats they
could support. Predation by rats (Rattus
sp.) and other introduced species may
also be significant. Surveys of roost
caves and sweeps in various locations in
American Samoa over the past year
indicate the Pacific sheath-tailed bat
may be there, however, no bats were
detected in 80 percent of the caves on
Tutuila. The listing priority number for
the Pacific sheath-tailed bat remains at
3, because the magnitude of the threats
facing the species is high, the threats are
imminent, and the taxon in question is
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 received on May 11, 2004. See
the information provided above (for the
Pacific sheath-tailed bat, semicaudata
subspecies) regarding the former range,
other subspecies, and threat the species
as a whole.
This subspecies formerly occurred on
Guam, and in the CNMI on Rota,
Aguiguan, Tinian, Saipan, and possibly
Anatahan and Maug. The Pacific sheathtailed bat is believed to be extirpated
from all islands in the Mariana Islands,
except Aguiguan. Predation by the
introduced brown treesnake (Boiga
irregularis) may have played a
significant role in the extirpation of the
species on Guam, and predation by rats
(Rattus sp.) and monitor lizards
(Varanus indicus) may also have been
significant factors in extirpations on
Guam and other islands. The 2003
surveys on Aguiguan, the only island
that still has a population of Pacific
sheath-tailed bats in the Marianas,
indicate the population is about 400–
500 animals. The Listing Priority
Number for the Pacific sheath-tailed bat
remains at 3, because the magnitude of
the threats facing the species is high, the
threats are imminent, and the taxon in
question is a subspecies.
Fisher, West Coast DPS (Martes
pennanti)—The following summary is
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24891
based on information in our files and in
the Service’s initial ‘‘warranted-butprecluded’’ 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. The fisher is
believed to be extirpated or reduced to
scattered individuals from the lower
mainland of British Columbia through
Washington, and in the central and
northern Sierra Nevada range in
California. Natural populations of the
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.
They also occur in the southern Cascade
Range in Oregon as descendants through
a reintroduction effort. There is a lack
of precise empirical data on West Coast
DPS fisher numbers. However, the lack
of detections over much of its historic
range, the high degree of genetic
relatedness within some populations,
and the fact that populations of native
fisher in California are separated by four
times the species’ maximum dispersal
distance, indicate that the likely extant
fisher populations are small and
apparently 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; standreplacing fire; Sudden Oak Death
Phytophthora; urban and rural
development; recreation development;
and roads. Major threats to fisher that
lead to direct mortality and injury
include collisions with vehicles,
incidental trapping of fisher during
trapping for other species, predation
and viral diseases such as rabies and
canine and feline distemper. Existing
regulatory mechanisms on Federal,
State, and private lands affect key
elements of fisher habitat, yet they
provide insufficient certainty that
conservation efforts will be
implemented or that they will be
effective in reducing the level of threats
to the West Coast DPS of the fisher.
However, the threats are nonimminent
as the remaining areas containing fisher
populations appear to be stable or not
rapidly declining. The greatest threats to
these remaining fisher populations are
issues related to small isolated
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populations and the potential for further
loss and fragmentation of habitat over
time. The listing priority number for
this DPS remains a 6 (threats are of a
high magnitude but are nonimminent).
Mazama pocket gopher (Thomomys
mazama (ssp. couchi, glacialis, louiei,
melanops, pugetensis, tacomensis,
tumuli, yelmensis)—See above in
‘‘Summary of Listing Priority Changes in
Candidates.’’ The above summary is
based on information contained in our
files and the petition received on
January 7, 2003.
Palm Springs round-tailed ground
squirrel (Spermophilus tereticaudus
chlorus)—See above in ‘‘Summary of
Listing Priority Changes in Candidates.’’
The above summary is based on
information in our files. No new
information was provided in the
petition received on May 11, 2004.
Southern Idaho ground squirrel
(Spermophilus brunneus endemicus)—
See resubmitted petition finding
published in the Federal Register on
December 27, 2004 (69 FR 77167).
Washington ground squirrel
(Spermophilus washingtoni)—See above
in ‘‘Summary of Listing Priority Changes
in Candidates.’’ The above summary is
based on information contained in our
files and the petition received on March
2, 2000.
Birds
Spotless crake, American Samoa DPS
(Porzana tabuensis)—See above in
‘‘Summary of Listing Priority Changes in
Candidates.’’ The above summary is
based on information contained in our
files. No new information was provided
in the petition received on May 11,
2004.
Kauai creeper (Oreomystis bairdi)—
See above in ‘‘Summary of Listing
Priority Changes in Candidates.’’ The
above summary is based on information
contained in our files. No new
information was provided in the
petition received on May 11, 2004.
Yellow-billed cuckoo, western U.S.
DPS (Coccyzus americanus)—See above
in ‘‘Summary of Listing Priority Changes
in Candidates.’’ The above summary is
based on information contained in our
files and the petition received on
February 9, 1998. See also our 12-month
petition finding published on July 25,
2001 (66 FR 38611).
Many-colored fruit-dove (Ptilinopus
perousii perousii)—See above in
‘‘Summary of Listing Priority Changes in
Candidates.’’ The above summary is
based on information contained in our
files. No new information was provided
in the petition received on May 11,
2004.
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Friendly ground-dove (Gallicolumba
stairi stairi)—See above in ‘‘Summary of
Listing Priority Changes in Candidates.’’
The above summary is based on
information contained in our files. No
new information was provided in the
petition received on May 11, 2004.
Streaked horned lark (Eremophila
alpestris strigata)—The following
summary is based on information
contained in our files and the petition
received on January 7, 2003. The
streaked horned lark is one of 21
subspecies of North American horned
larks. According to recent genetic
analyses, this subspecies is unique,
isolated, and has little genetic diversity,
indicating it has been evolving
independently for some time.
Historically, the breeding range
extended from southern British
Columbia, south through the Puget
lowlands and along the Washington
coast, and through the Willamette
Valley of Oregon. Currently, the
subspecies is extirpated in British
Columbia. Only 11 breeding sites are
known in Washington, and the breeding
population in Oregon is estimated to
include less than 300 birds. Threats
include loss and degradation of habitat
due to conversion of native grassland to
other uses, encroachment of woody
vegetation due to fire suppression,
invasion of habitat by nonnative plants
and animals, human disturbance, nest
predation, deposition of dredge spoil,
and conflict with airport development
and maintenance activities. The
magnitude of threats is high because few
individuals are found in a small number
of populations having patchy, isolated
distributions in habitats highly desirable
for development and threatened by
invasive plant species. Populations
occur in suitable habitat on airports and
military bases, where management and
training activities can affect breeding.
Specific threats are not known to be
imminent, and some conservation
measures have been initiated by land
managers. The LPN for this subspecies
remains a 6.
Kittlitz’s murrelet (Brachyramphus
brevirostris)—The following summary is
based on information contained in our
files and the petition 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. Most recent
population estimates (9,500–26,700
birds) indicate that it has the smallest
population of any seabird considered a
regular breeder in Alaska. This species
appears to have undergone significant
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population declines in four of its core
population centers—Prince William
Sound, Malaspina Forelands, Glacier
Bay, and Kenai Fjords. As populations
become smaller, they become
increasingly vulnerable to events that
may result in local extirpation. Causes
for the declines in populations are not
well known, but we believe that glacial
retreat and oceanic regime shifts are the
most likely causes. Kittlitz’s murrelets
seem to prefer areas near stable or
advancing tidewater glacier faces as
these areas have higher primary
productivity compared to siltier, less
saline fjords with receding glaciers, but
the ecological mechanisms linking
Kittlitz’s murrelets to their preferred
habitats remains a topic for further
research. Other causes of decline may
include: habitat loss or degradation,
increased adult and juvenile mortality,
and low recruitment. Existing regulatory
mechanisms appear inadequate to stop
or reverse population declines or to
reduce the threats to this species. Due
to the nonimminent threats of high
magnitude, we are retaining a listing
priority number of 5 for this species.
Xantus’s murrelet (Synthliboramphus
hypoleucus)—See above in ‘‘Summary
of Listing Priority Changes in
Candidates.’’ The above summary is
based on information contained in our
files and the petition received on April
16, 2002.
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 12month 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,
cumulative habitat degradation caused
by severe grazing, woody plant invasion
of open prairies, fire suppression,
herbicides, 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 properties affected by these
individual threats. We view current and
continued habitat fragmentation to be a
serious ongoing threat that facilitates the
extinction process through several
mechanisms: remaining habitat patches
may become smaller than necessary to
meet the yearlong requirements of
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individuals and populations, necessary
habitat heterogeneity may be lost to
large areas of monoculture vegetation
and/or homogenous habitat structure,
areas between habitat patches may
harbor high levels of predators or brood
parasites, and the probability of
recolonization decreases as the distance
between suitable habitat patches
expands.
The Service is currently working to
quantify the ongoing level of habitat
fragmentation throughout the species
range. Although Federal lands comprise
only five percent of currently occupied
habitat, these tracts are located in areas
essential to population recovery and
dispersal. As a result, the Service views
habitat management considerations on
Federal lands within current and
historic range as very important. Due to
their potential magnitude to affect the
species, current planning efforts for
grazing and wind, oil, and gas
development on public lands is of
particular relevance to the future listing
status of the species.
Based on all currently available
information, we find that ongoing
threats to the lesser prairie-chicken, as
outlined in the 12-month finding,
remain unchanged and lesser prairiechickens continue to warrant Federal
listing as threatened. We have
determined that the overall magnitude
of threats to the lesser prairie-chicken
throughout its range are moderate, and
that the threats are ongoing; thus, they
are considered imminent. Consequently,
a listing priority number of 8 remains
appropriate for the species. Greater sagegrouse, Columbia Basin DPS
(Centrocercus urophasianus)—We have
not updated our finding with regard to
the Columbian Basin DPS of the greater
sage-grouse in this notice. In the
previous CNOR, we found that a listing
proposal for this DPS was still
warranted but precluded by higher
priorities, and we assigned the DPS a
listing priority number of 6. Since that
time, new information has become
available through the status review of
the greater sage-grouse (range-wide). We
will use the best scientific and
commercial information available
(including, but not limited to
information that became available
during the rangewide status review) to
reevaluate whether the Columbia Basin
population still qualifies as a DPS under
our DPS policy, and if it does, whether
the DPS still warrants a listing proposal.
Once that evaluation is completed we
will publish an updated finding for this
DPS in the Federal Register either in the
next CNOR or in a separate notice.
Gunnison sage-grouse (Centrocercus
minimus)—The following summary is
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based on information contained in our
files and the petition received on
January 25, 2000. For greater detail, also
see 65 FR 82310 (December 28, 2000).
The range of the Gunnison sage-grouse
has been reduced to less than 25 percent
of it historical range, distributed across
8 populations. Size of the range and
quality of its habitat have been reduced
by direct habitat loss, habitat
fragmentation, and habitat degradation
from building development, road and
utility corridors, fences, energy
development, conversion of native
habitat to hay or other crop fields,
alteration or destruction of wetland and
riparian areas, inappropriate livestock
management, and creation of large
reservoirs. Numerous conservation
actions have occurred and funding and
plans for additional conservation
actions are in place or ongoing. Despite
these actions, sage-grouse numbers
declined significantly in 2003 (likely
due to the 2002 drought) and remained
at a low level in 2004. Given ongoing
and potential individual and cumulative
threats, we are leaving the listing
priority at a 2 at this time.
Band-rumped storm-petrel, Hawaii
DPS (Oceanodroma castro)—The
following summary is based on
information contained in our files and
the petition 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, widespread seabird found in
the subtropics of the 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.
The species is currently known to nest
only on Kauai but is suspected to nest
on Hawaii. Although small populations
do occur on Maui and Hawaii, we have
been unable to determine if they are
viable; certainly they are not large and
they represent a fraction of prehistoric
distribution. The current primary
threats to the species, predation by
nonnative species and mortality
associated with disorientation by lights,
have been occurring for several decades,
and are affecting a large proportion of
the population.
Predation by introduced species has
played a significant role in reducing
storm-petrel numbers and exterminating
colonies in the Pacific and other
locations worldwide. Several alien
predators are found throughout the
main Hawaiian Islands, including
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Polynesian rats (Rattus exulans), black
rats (R. rattus), Norway rats (R.
norvegicus), feral and domestic cats
(Felis catus), small Indian mongooses
(Herpestes auropunctatus), and barn
owls (Tyto alba). Band-rumped stormpetrels nest only in remote, steep, rocky
areas, probably because these areas are
less accessible to predators. Artificial
lighting of roadways, resorts, ballparks,
residences and other developments
attracts and confuses night-flying,
storm-petrel fledglings, resulting in
‘‘fall-out’’ and collisions with buildings
and other objects. ‘‘Fall-out’’ is a term
used to describe when fledglings are
attracted to lights, become disoriented
and fall to the ground where they are
often killed by cars or predators. Over
a 12-year period from 1978 to 1990,
Harrison et. al. reported that 15 bandrumped storm-petrels, 13 of which were
young, were recovered on Kauai as a
result of fall-out. The impact from
artificial lighting is expected to increase
as human population grows and
development continues on Kauai and
other Hawaiian Islands. The total
population size is poorly known, but is
unlikely to number more than a few
hundred pairs. The listing priority
number for the band-rumped stormpetrel remains at 3, because the
magnitude of the threats facing the
species is high, the threats are
imminent, and the taxon in question is
a distinct population segment.
Elfin woods warbler (Dendroica
angelae)—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 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.
Habitat destruction from expansion of
public facilities, sun coffee plantations,
timber management, disruption of
breeding activities, potential predators,
and catastrophic natural events threaten
this species. These threats are not
imminent because most of the range of
this species is within protected lands.
The listing priority number remains a 5
for this species.
Reptiles
Sand dune lizard (Sceloporus
arenicolus)—see resubmitted petition
finding published in the Federal
Register on December 27, 2004 (69 FR
77167).
Eastern massasauga (Sistrurus
catenatus catenatus)—The following
summary is based on information
contained in our files. No new
information was provided in the
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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
considered imperiled in every state and
province it occupies. Each state and
Canadian province across the range of S.
c. catenatus has lost more than 30
percent, and for the majority more than
50 percent of their historical
populations. Furthermore, less than 35
percent of the remaining populations
are considered secure.
Approximately 59 percent of the
remaining S. c. catenatus populations
occur wholly or in part on public land,
and State-wide and/or site-specific
Candidate Conservation Agreements
with Assurances (CCAAs) are currently
being developed for many of these areas
in Iowa, Illinois, Michigan, Missouri,
Ohio, and Wisconsin. Populations soon
to be under CCAs and CCAAs are
expected to have a high likelihood of
persisting and remaining viable. Other
populations are likely to suffer
additional losses in abundance and
genetic diversity and some will likely be
extirpated unless threats are removed in
the near future. Therefore, the
magnitude of threats from habitat
modification, habitat succession,
incompatible land management
practices, illegal collection for the pet
trade, and human persecution is
moderate overall with most imminent
threats occurring to remaining
populations on private lands. Due in
large part to the numerous CCAAs
currently being developed and
implemented, we do not believe
emergency listing is warranted and have
kept the listing priority number at 9 for
this eastern massasauga 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 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
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Mobile River Delta. Black pine snake
surveys and trapping indicate that this
species has been extirpated from
Louisiana and from two 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 species. Most of the known
Mississippi populations are
concentrated in the DeSoto National
Forest. Populations in Alabama occupy
private, nonindustrial timberland where
they have an uncertain future due to
habitat loss and degradation. Other
factors affecting the black pine snake
include vehicular mortality and low
reproductive rates which magnify other
threats and increase the likelihood of
local extinctions. Due to nonimminent
threats of high magnitude caused by the
past destruction of most of the longleaf
pine habitat of the black pine snake, and
persistent degradation of what remains,
we are retaining a listing priority
number of 6 for this subspecies.
Louisiana pine snake (Pituophis
ruthveni)—The following summary is
based on information contained in our
files and the petition received on July
19, 2000. The Louisiana pine snake
historically occurred in fire-maintained
longleaf pine ecosystems of west-central
Louisiana and extreme east-central
Texas. Louisiana pine snakes are closely
associated with Baird’s pocket gophers
(Geomys breviceps) and make extensive
use of their burrow systems for foraging,
nocturnal and diurnal retreats, escape
from predators and fire, and for
hibernation sites. Within some of the
best remaining habitat in their historic
range, Louisiana pine snakes have not
been documented in over a decade.
Results of Louisiana pine snake trapping
and radiotelemetry surveys suggest that
extensive population declines and local
extirpations have occurred during the
last 50 to 80 years.
Most of the historical longleaf pine
habitat of the Louisiana pine snake has
been destroyed, and the habitat quality
of that which remains has been
degraded due to logging, fire
suppression, roadways, short-rotation
silviculture, and grazing. Louisiana pine
snake habitat loss is continuing, albeit at
a slower rate than in the past. The best
remaining Louisiana pine snake habitat
occurs on lands where periodic burning
has continued. Other factors affecting
Louisiana pine snakes include low
fecundity (reproductive output), which
magnifies other threats and increases
the likelihood of local extinctions, and
vehicular mortality, which may
significantly effect Louisiana pine snake
population and community structure.
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The Candidate Conservation
Agreement for the Louisiana pine snake,
a comprehensive and voluntary
partnership encompassing all Federal
lands where pine snake occurrences are
known, was recently completed in order
to protect known Louisiana pine snake
populations and maintain the ecosystem
upon which it depends. Several private
landowners with known Louisiana pine
snake populations are interested in
joining that partnership or developing a
similar one. Nevertheless, while the
magnitude of Louisiana pine snake
habitat loss is great and the remaining
habitat is degraded, continued habitat
loss does not represent an imminent
threat, because the rate of habitat loss
appears to be declining, and pro-active
partnerships to address key
management concerns and research
needs are growing. Due to nonimminent
threats of a high magnitude, we
continue to assign a listing priority
number of 5 to this species.
Cagle’s map turtle (Graptemys
caglei)—The following summary is
based on information contained in our
files and the petition received on April
26, 1991. Cagle’s map turtle occurs in
scattered population sites within seven
counties in Texas along the Guadalupe,
San Marcos, and Blanco Rivers. Loss
and degradation of riverine habitat from
large and/or small impoundments (dams
or reservoirs) is the primary threat to the
Cagle’s map turtle. One effect of
impoundment is the loss of riffle and
riffle/pool transition areas used by
males for foraging. Depending on its
size, a dam itself may be a partial or
complete barrier to Cagle’s map turtle
movement and could fragment
populations. Construction of smaller
impoundments and human activities on
rivers occupied by the Cagle’s map
turtle have likely eliminated or reduced
foraging and basking habitats in the
past. Although the water plan in
development by the State of Texas is
considering reservoirs that have the
potential to alter or destroy habitat for
this species, firm plans for new
reservoir construction have not been
made. Cagle’s map turtle is also
vulnerable to overcollecting and target
shooting. Based on the high magnitude
of nonimminent threats, we retain a
listing priority of 5 for this species.
Sonoyta mud turtle (Kinosternon
sonoriense longifemorale Iverson)—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
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
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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 turtle occurs is one of
the driest regions of the southwest. Due
to continuing irrigated agriculture and
development in the region, surface
water in the Rio Sonoyta can be
expected to dwindle further. This
species may also be vulnerable to aerial
spraying of pesticides on nearby
agricultural fields. Due to imminent
threats of a high magnitude, we are
keeping the listing priority number of 3
for this subspecies.
Amphibians
Columbia spotted frog, Great Basin
DPS (Rana luteiventris)—The following
summary is based on information
contained in our files and the petition
received on May 1, 1989. Currently,
Columbia spotted frogs appear to be
widely distributed throughout
southwestern Idaho, eastern Oregon,
northeastern and central Nevada, and
southeastern Washington, 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.
Habitat degradation and fragmentation
is probably a combined result of past
and current influences of heavy
livestock grazing, spring alterations,
agricultural development, urbanization,
beaver control, and mining activities.
Fragmentation of habitat may be one of
the most significant barriers to
Columbia spotted frog recovery and
population persistence. Loss of
vegetation and/or lowering of the water
table as a result of the above mentioned
activities can significantly threaten frogs
moving from one area to another.
Likewise, fragmentation and loss of
habitat can prevent frogs from
colonizing suitable sites elsewhere.
Two conservation agreements and
strategies were signed by Federal, State,
County, and university representatives
on September 30, 2003, for the central
and northeast Nevada subpopulations.
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 significant portion of
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their historic 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 historic range within those areas.
Although these agreements may reduce
threats in the future, we retained a
listing priority number of 3 for this DPS
of the Columbia spotted frog because the
threats are imminent and of a high
magnitude.
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). The mountain yellowlegged frog is restricted to two disjunct
areas in California and a portion of
Nevada. One area is in the Sierra
Nevada and the other area is in southern
California (Los Angeles, San
Bernardino, Riverside, and San Diego
Counties). The 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 in national forests and
national parks. Rangewide, it is
estimated that the number of mountain
yellow-legged frog populations has
undergone a 50 to 80 percent reduction.
Direct predation by nonnative fishes
has resulted in rangewide population
declines and local extirpations.
Furthermore, the result of these
extirpations is that the remaining
populations are fragmented and
isolated, making them vulnerable to
further declines and local extirpations
caused by other factors such as disease.
In a recent study, from 1996 to 2003,
introduced trout were removed from 5
lakes in a remote area of the Sierra
Nevada, with 16 nearby lakes used as
controls. The experiment concluded
that introduced trout are effective
predators on mountain yellow-legged
frog tadpoles, and suggested ‘‘(i) that the
introduction of trout is the most likely
mechanism responsible for the decline
of this mountain frog and (ii) that these
negative effects can be reversed.’’ To
help reverse the decline of the mountain
yellow-legged frog, the Sequoia and
Kings Canyon National Parks have been
removing introduced trout since 2001,
and efforts are continuing through the
2004 season. It is likely that disease,
specifically chytrid fungus, has also
caused the recently observed declines in
the species. Although the life history
and modes of transmission of chytrid
fungus are not well understood, it
appears that this pathogen is
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widespread throughout the range of the
mountain yellow-legged frog within the
Sierra Nevada, it is persistent in
ecosystems, and it is resilient to
environmental conditions such as
drought and freezing.
We conclude that all remaining
mountain yellow-legged frog
populations within the Sierra Nevada
are at risk of declines and extirpation
primarily as a result of predation by
introduced trout and infection by
pathogens. We conclude that the overall
magnitude and immediacy of threats to
the Sierra Nevada distinct population
segment of the mountain yellow-legged
frog is high. Therefore, we retain a
listing priority of 3 for this DPS.
Oregon spotted frog (Rana pretiosa)—
The following summary is based on
information contained in our files and
the petition 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 threats to the species’ habitat
include development, livestock grazing,
introduction of nonnative plant species,
changes in hydrology due to
construction of dams and alterations to
seasonal flooding, and poor water
quality. Additional threats to the species
are predation by nonnative fish and
introduced bullfrogs. The high
magnitude of threat is due to small
populations with patchy and isolated
distributions and the wide range of
threats to both individuals and their
habitats. Habitat restoration and
management actions have not prevented
a decline in the reproductive rates in
some populations. Each population is
faced with multiple actual and potential
threats that could seriously reduce or
eliminate any of these isolated
populations and further reduce the
range of the species. Based on these
threats, we retain a listing priority 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 received on May 9, 2002.
Relict leopard frogs are currently known
to occur naturally in two general areas
of Nevada—near the Overton Arm area
of Lake Mead and Black Canyon below
Lake Mead. In addition to these natural
sites, three translocation sites have been
established, two in Nevada and one in
Arizona. We estimate that the current
distribution is less than 20 percent of
the historical distribution. As habitat
generalists, relict leopard frogs likely
occupied a variety of habitats including
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springs, streams, and wetlands
characterized by clean, clear water, in
both deep and shallow water, and
cover/forage such as submerged,
emergent, and perimeter vegetation.
The causes for the population
declines of this species are not entirely
clear, but suggested factors include
alteration of aquatic habitat due to
agriculture and water development, and
the introduction of exotic predators and
competitors. The magnitude of threats to
the relict leopard frog are high based on
its limited numbers and distribution,
the presence of nonnative predators,
potential alteration of remaining habitat
including groundwater pumping, and
diversion of surface water. We do not
consider threats to be imminent at this
time. Although the numbers are low and
distribution is limited, efforts are
underway to improve habitat and
increase numbers through captive
rearing and translocation. There are no
proposed projects that may result in
further habitat degradation. In addition,
a conservation agreement and strategy is
being developed which is intended to
improve the status of the species
through prescribed management actions
and protection. The effectiveness of the
plan in achieving adequate conservation
for the relict leopard frog will remain
unknown until the plan is completed
and implementation is initiated.
Therefore, we retain a listing priority of
5 for the relict leopard frog.
Ozark hellbender (Cryptobranchus
alleganiensis bishopi)—See above in
‘‘Summary of Listing Priority Changes in
Candidates.’’ The above summary is
based on information contained in our
files. No new information was provided
in the petition received on May 11,
2004.
Austin blind salamander (Eurycea
waterlooensis)—The following summary
is based on information in our files. No
new information was provided in the
petition received on May 11, 2004. The
Austin blind salamander is known to
occur in and around three of the four
spring sites that comprise the Barton
Springs complex in the City of Austin,
Travis County, Texas.
Primary threats to this species are
degradation of water quality and
quantity due to expanding urbanization.
The Austin blind salamander depends
upon a constant discharge of clean
water from the Edwards Aquifer for its
survival. Urbanization can dramatically
alter the normal hydrologic regime and
water quality of an area. An increase in
impervious cover (i.e. impervious to
normal drainage) as a result of
development increases the quantity and
velocity of runoff that leads to erosion
and greater pollution transport.
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Pollutants and contaminants that enter
the Edwards Aquifer are discharged in
salamander habitat at Barton Springs
and may have serious morphological
and physiological effects to the
salamander. As the human population
increases in central Texas, the demand
on groundwater sources increases.
Increased pumping of the Edwards
Aquifer can result in reduced
springflows that may also detrimentally
impact the salamander. Based on the
high magnitude of the imminent threats
imposed on this species, we are
retaining a listing priority number of 2
for this species.
Georgetown salamander (Eurycea
naufragia)—The following summary is
based on information 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 upon a
constant discharge of clean water from
the Edwards Aquifer for its survival.
Primary threats to this species are the
same as for the Austin blind salamander
above. With imminent threats of high
magnitude, we retain a listing priority of
2 for this species.
Salado salamander (Eurycea
chisolmensis)—The following summary
is based on information in our files. No
new information was provided in the
petition 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.
Salamanders have not been located at
Robertson Springs since 1991. Primary
threats to this species are habitat
modification and degradation of water
quality and quantity due to expanding
urbanization. Many of the spring outlets
in the City of Salado have been
modified by dam construction. Because
Big Boiling Springs is located near
Interstate 35 and in the center of the
city, increasing traffic and urbanization
bring increased threats of contamination
spills, higher levels of impervious cover,
and subsequent impacts to groundwater.
The Salado salamander depends upon a
constant discharge of clean water from
the Edwards Aquifer for its survival.
Pollutants and contaminants that enter
the Edwards Aquifer can be discharged
in salamander habitat, and may cause
serious morphological and physiological
effects to the salamander. As the human
population increases in central Texas,
greater demand on groundwater sources
occurs. Increased pumping of the
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Edwards Aquifer can result in reduced
springflows that may also detrimentally
impact the salamander. With imminent
threats of high magnitude, we are
retaining a listing priority number of 2
for this salamander species.
Boreal toad, Southern Rocky
Mountains DPS (Bufo boreas boreas)—
The following summary is based on
information contained in our files and
the petition received on September 30,
1993. See also our 12-month petition
finding published on March 23, 1995
(60 FR 15281). The boreal toad (Bufo
boreas) can be found throughout most of
the mountainous regions of the western
United States and was considered
common throughout the southern Rocky
Mountains (southeastern Wyoming to
northern New Mexico). The abundance
of the species in the southern Rocky
Mountains has declined significantly in
the past few decades. While there are 32
populations, only one population in
Colorado is considered viable. In the
southern Rocky Mountains, the disease
chytridiomycosis, resulting from the
chytrid fungus Batrachochytrium
dendrobatidis, is the primary threat to
the boreal toad. This fungus is only
known to infect amphibians and is the
primary suspect in the decline of
numerous amphibian species around
the world. It is unknown why this
fungus has become a problem over the
past few decades, or how it moves from
one population to another. We continue
to give the toad a listing priority of 3,
because chytrid fungus infection is an
ongoing threat of high magnitude and is
likely to extirpate additional infected
boreal toad populations.
Yosemite toad (Bufo canorus)—The
following summary is based on
information contained in our files and
the petition received on April 3, 2000.
See also our 12-month petition finding
published on December 10, 2002 (67 FR
75834). The historical range of Yosemite
toads in the Sierra Nevada occurs from
the Blue Lakes region north of Ebbetts
Pass to 5 kilometers (km) (3.1 miles
(mi)) south of Kaiser Pass in the
Evolution Lake/Darwin Canyon area.
Alteration and loss of habitat due to
grazing, timber management, water
diversion, recreation, and vegetative/fire
management are threats. The decline of
some populations of the Yosemite toad
has been attributed to the effects of
poorly managed livestock grazing. The
levels of timber harvest and road
construction have declined substantially
since implementation of the California
Spotted Owl Sierran Province Interim
Guidelines in 1993, and some existing
roads have been, or are scheduled for,
decommissioning. Therefore, the risks
posed by new roads and timber harvests
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have declined, but those already
existing still pose risks to the species
and its habitat through erosion,
vehicular mortality, and contaminant
introduction. Due to their water depth,
reservoirs represent both a loss of
habitat and a barrier to dispersal. In
addition, the evidence of an adverse
physiological effect of pesticides on
Sierra Nevada amphibians in the field
indicates that contaminants may be a
risk to the Yosemite toad and may have
contributed to the species’ decline.
These factors have probably contributed
to the decline of Yosemite toads and
currently pose a risk to the species. We
determined the magnitude of threats to
be moderate, rather than high, because
almost all of the species’ range occurs
on Federal land, which facilitates
management of the species by Federal
agencies. We determined the threats to
the Yosemite toad to be nonimminent.
Therefore, we retain a listing priority
number of 11 for the Yosemite toad.
Black Warrior waterdog (Necturus
alabamensis)—See above in ‘‘Summary
of Listing Priority Changes in
Candidates.’’ The above summary is
based on information contained in our
files. No new information was provided
in the petition received on May 11,
2004.
Fishes
Arkansas darter (Etheostoma
cragini)—The following summary is
based on information from our files. No
new information was provided in the
petition received on May 11, 2004. The
Arkansas darter is a fish with
widespread distribution throughout the
Arkansas River basin in Arkansas,
Kansas, Colorado, Missouri, and
Oklahoma. Threats to this species
include water quantity depletion such
as withdrawal of groundwater within
the Arkansas River basin in Kansas,
water quality degradation resulting from
increased urbanization and agricultural
activities, and genetic isolation. The
most recent survey data indicate the
Arkansas darter still persists at
numerous locations which are widely
distributed, providing some measure of
protection against extirpation resulting
from a single randomly occurring event.
Data also indicate groundwater
withdrawal in a significant portion of
the species’ range has declined in the
last decade. The overall impacts facing
this species have been reduced to the
point where they represent a low to
moderate magnitude threat. Because of
these factors, we retain a listing priority
of 11 for this species.
Cumberland Johnny darter
(Etheostoma nigrum susanae)—The
following summary is based on
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information from our files. No new
information was provided in the
petition received on May 11, 2004. The
Cumberland Johnny darter is a small
(approximately 3 inches) member of the
family Percidae. The Cumberland
Johnny darter is endemic to the upper
Cumberland River system, above
Cumberland Falls, in Kentucky, and
Tennessee. According to recent surveys,
it appears that the subspecies is
restricted to 16 small streams in Whitley
and McCreary Counties, Kentucky, and
2 streams in Scott and Campbell
Counties, Tennessee. Based on these
surveys, formerly reported populations
in Little Wolf Creek, Whitely County,
Kentucky, Gum Fork, Scott County,
Tennessee, and the mainstem of the
Cumberland River appear to have been
extirpated.
The Cumberland Johnny darter
inhabits shallow water in low velocity
shoals or riffles and backwater areas of
moderate to low gradient stream reaches
with stable sand or sandy-gravel
substrates. Existing populations of
Cumberland Johnny darter are small in
size and range and are geographically
isolated from one another. This patchy
distribution makes them more
susceptible to extirpation from single
events of large impact. It also reduces
their ability to recover from smaller
impacts to their habitat or population
size. This level of isolation makes
natural repopulation of any extirpated
population impossible without human
intervention. Population isolation also
inhibits the natural interchange of
genetic material between populations;
some of the Cumberland Johnny darter
populations are likely below the
effective population size required to
maintain long-term genetic and
population viability.
Siltation, primarily from coal mining
activities but also from forestry and
agricultural activities, road
construction, and urban development,
appears to be the major factor
contributing to the decline of the
Cumberland Johnny darter. Federal and
State water quality laws have reduced
water quality threats to some degree, but
non-point pollution threats and
modification of instream habitat and
hydrology are cumulative and gradual.
Consequently, we continue to assign the
Cumberland Johnny darter a listing
priority number of 6, reflecting a threat
magnitude and immediacy of high and
nonimminent, respectively.
Pearl darter (Percina aurora)—The
following summary is based on
information from our files. No new
information was provided in the
petition received on May 11, 2004. Little
is known about the specific habitat
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requirements of the pearl darter. Pearl
darters have been collected from gravel
riffles and rock outcrops; deep runs over
gravel and sand pools below shallow
riffles; swift, shallow water over firm
gravel and cobble in mid-river channels;
swift water near brush piles and scour
holes. The pearl darter is historically
known only from localized sites within
the Pearl and Pascagoula River
drainages in Mississippi and Louisiana.
The pearl darter is very rare in the
Pascagoula River system and is extinct
in the Pearl River system. Since 1983,
pearl darters have only been found in
scattered sites within the Pascagoula
drainage, including the Pascagoula,
Chickasawhay, Chunky, Leaf, and Bouie
Rivers and Okatoma and Black Creeks,
resulting in a 66 percent decrease of
range. The pearl darter is vulnerable to
nonpoint source pollution, changes in
river and stream geomorphology, and
other human-induced threats to its
environment. The magnitudes of threats
to the pearl darter are high based on its
limited numbers and distribution.
However, we do not consider threats to
be imminent at this time. Although the
numbers are low and distribution is
disjunct, efforts are underway to
improve habitat by reducing
sedimentation and increase numbers of
pearl darters through husbandry. There
are no known proposed projects that
may result in further habitat degradation
at this time. Therefore, we retain a
listing priority number of 5 for the pearl
darter.
Rush darter (Etheostoma
phytophilum)—The following summary
is based on information from our files.
No new information was provided in
the petition received on May 11, 2004.
The life history of the rush darter is
poorly known. Rush darters have been
collected in vegetation from very
shallow, clear, cool and flowing water.
Rush darters appear to prefer relatively
low-gradient small streams, not
necessarily spring influenced.
Historically, rush darters have been
found in three distinct watersheds in
Alabama: Clear Creek drainage in
Winston County; Turkey Creek drainage
in Jefferson County; and Little Cove and
Bristow Creek in Etowah County.
Cumulatively, the rush darter is only
known from localized collection sites
within approximately 14 km (9 miles) of
streams in the mentioned counties.
The rush darter is currently known to
have one of the most restricted
distributions of any vertebrate in
Alabama and all are located above the
Fall Line in the Tombigbee-Black
Warrior drainage. There are only two
known extant rush darter populations:
the Clear Creek drainage in Winston
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County and the Beaver Creek and Penny
Springs areas in the Turkey Creek
drainage in Jefferson County. The rush
darter is vulnerable to non-point source
pollution, urbanization, and changes in
stream geomorphology due to its
localized distribution in parts of two
unconnected stream drainages and its
apparent low population sizes.
Sedimentation has been identified as
the greatest threat to the rush darter.
Industrialization is extensive
throughout the rush darter’s habitat,
particularly near the type locality for the
rush darter in Jefferson County.
Although efforts are underway to
improve habitat by reducing
sedimentation and increase numbers of
rush darters through husbandry, the
magnitude of threats to the rush darter
are high based on its limited numbers
and distribution. We do not consider the
threats to be imminent at this time,
however, as we know of no proposed
projects that may result in further
habitat degradation. Therefore, we
retain a listing priority number of 5 for
the rush darter.
Yellowcheek darter (Etheostoma
moorei)—The following summary is
based on information from our files. No
new information was provided in the
petition received on May 11, 2004. The
Yellowcheek darter is endemic to only
four headwater tributaries of the Little
Red River, Arkansas. It is vulnerable to
alterations in physical habitat
characteristics such as the
impoundment of Greers Ferry Reservoir,
channel maintenance in the Archey
Fork tributary, increased sedimentation
from eroding stream banks and poor
riparian management (e.g. livestock
grazing in and along tributaries resulting
in higher sediment loads), and illegal
gravel mining. Factors affecting the
remaining populations include loss of
suitable breeding habitat, habitat and
water quality degradation, population
isolation, and severe population
declines.
The Middle Fork tributary was listed
as an impaired waterbody by the
Arkansas Department of Environmental
Quality in 2004 due to excessive
bacteria and low dissolved oxygen.
Recent studies have documented
significant declines in the numbers
(60,000 in 1981 compared to 10,300 in
2000) of this fish in the remaining
populations and further range
restriction within the tributaries (130.4
to 65.0 stream km). As a result,
yellowcheek darter numbers have
declined by 83 percent in both the
Middle Fork and South Fork, and by 60
percent in the Archey Fork during the
past 20 years. No yellowcheek darters
were found in the Devils Fork during a
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2000 status survey; the species has
apparently been extirpated in that reach.
A comparison of inhabited stream
reaches in a 1981 survey versus the
2000 survey reveals that the largest
decline occurred in the South Fork,
where reaches formerly inhabited by the
yellowcheek darter declined by 70
percent. The second largest decline
occurred in the Archey Fork, where
there was a 60 percent reduction in
inhabited stream reach. The Middle
Fork showed the least decline in
inhabited stream reach, at 22 percent.
Due to imminent threats of a high
magnitude, we retain a listing priority
number of 2 for this species.
Fluvial arctic grayling, upper
Missouri River DPS (Thymallus
arcticus)—The following summary is
based on information contained in our
files and the petition received on
October 2, 1992. See also our 12-month
petition finding published on July 25,
1994 (59 FR 37738). The distinct
vertebrate population segment (DPS) of
fluvial Arctic grayling (Thymallus
arcticus) of the upper Missouri River
once ranged throughout the streams and
rivers of the upper Missouri River
drainage above Great Falls. Currently,
the only confirmed fluvial population is
restricted to the upper Big Hole River in
Montana, an area estimated to be less
than 5 percent of the population
segment’s historical range. Attempts
since 1997 to re-establish additional
populations in historic waters have not
yet produced any self-sustaining
populations.
The primary threats facing the fluvial
Arctic grayling are hydrologic
alterations and stream dewatering from
irrigation withdrawals, thermal stress,
degradation and loss of riparian habitat,
entrainment in irrigation ditches, lack of
fish passage, and encroachment by
nonnative trout species. Since 1999,
persistent drought in southwestern
Montana has exacerbated the effects of
these primary threats, and
corresponding survey data do not
suggest a secure fluvial Arctic
population in the Big Hole River.
Consequently, we elevated the listing
priority for fluvial Arctic grayling from
a 9 to a 3 in the 2003 CNOR.
In May 2004, stream flows in the
upper Big Hole River reached critically
low levels because of early snowmelt
runoff and irrigation withdrawals. On
May 18, 2004, the Center for
Biodiversity (CBD) sent a letter to us
requesting we emergency list the
grayling based on the ‘‘critical
situation’’ caused by low streamflows.
Federal agencies, State agencies, and
private landowners addressed the low
streamflows with a collaborative effort
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to improve flows by withdrawing land
from irrigation and installing off-stream
livestock watering facilities. Timely
precipitation, supplemented by the
above voluntary conservation actions,
helped maintain discharge above
minimum ‘‘survival’’ levels for fluvial
Arctic grayling in the upper Big Hole
River through the remainder of 2004, so
the ‘‘critical situation’’ cited in CBD’s
emergency listing request did not
persist. Fluvial Arctic grayling persist at
low abundance in the Big Hole River
and a number of associated tributary
streams, and recent spawning success
observed in 2003–04 is consistent with
a functional, albeit depressed,
population. Thus, emergency listing is
not warranted at this time (see also the
2003 CNOR published on May 4, 2004,
for our determination that emergency
listing was not warranted at that time);
however, a listing priority of 3
continues to be warranted because the
threats facing the DPS remain high in
magnitude and imminent. We are
closely monitoring the status of this DPS
and ongoing efforts to secure the Big
Hole River population and expand its
range into historic waters in the upper
Missouri River basin.
Chucky madtom (Noturus sp. cf. N.
elegans)—The following summary is
based on information from our files. No
new information was provided in the
petition received on May 11, 2004. The
chucky madtom is a rare, undescribed
catfish known from only 14 specimens
collected from two Tennessee streams.
A lone individual was collected in 1940
from Dunn Creek (a Little Pigeon River
tributary) in Sevier County, and 13
specimens have been encountered since
1991 in Little Chucky Creek (a
Nolichucky River tributary) in Greene
County. Only 3 specimens have been
encountered since 1994 from two riffle
areas in a short reach of Little Chucky
Creek. All Little Chucky Creek
specimens have been collected from
stream runs with slow to moderate
current over pea gravel, cobble, or slabrock substrates.
The majority of the Little Chucky
Creek watershed is privately owned and
managed for beef cattle production,
tobacco cultivation, and row crops,
especially corn and soybeans. The Dunn
Creek watershed shares these same
agricultural practices. Nonpoint source
sediment and agrochemical inputs from
local agricultural and other sources may
adversely affect the chucky madtom by
altering the physical characteristics of
its habitat, thus potentially impeding its
ability to feed, seek shelter from
predators, and successfully reproduce.
The Service believes that potential
demographic effects of inbreeding,
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restricted distribution, and low number
of individuals pose imminent threats to
the chucky madtom in its only known
extant and historic locations. We are
retaining a listing priority number of 2
for the chucky madtom.
Grotto sculpin (Cottus sp., sp. nov.)—
The following summary is based on
information from our files. No new
information was provided in the
petition received on May 11, 2004. The
Grotto sculpin is a small fish within the
banded sculpin taxonomic complex that
exhibits cave-adapted features,
including nearly nonfunctional eyes,
reduced skin pigmentation, and smaller
optic nerves. The species inhabits pools
and riffles within cave systems in two
karst (cave) areas in Perry County,
Missouri. Only a few thousand
individuals are thought to exist. The
species is threatened by water quality
contamination as a result of point and
nonpoint pollution sources. A large dieoff of all Grotto sculpins in one of the
five known occupied cave systems
known to have the species was likely a
result of pollution. The species is also
threatened by predatory fish that likely
prey upon Grotto sculpin and are
known from all locations occupied by
the species. These predators, normally
excluded from cave environments,
escape surface farm ponds that
unexpectedly drain through sinkholes
into the underground cave systems and
enter grotto sculpin habitat. Currently
no State or Federal regulations provide
protection for the Grotto sculpin. Due to
imminent threats of a high magnitude,
a listing priority number of 2 remains
appropriate for this species.
Sharpnose shiner (Notropis
oxyrhynchus)—The following summary
is based on information from our files.
No new information was provided in
the petition 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.
Current information indicates that the
population within the Upper Brazos
River drainage (upstream of Possum
Kingdom Reservoir) is apparently stable,
while the population within the Middle
and Lower Brazos River Basins may
only exist in remnant areas of suitable
habitat, or may be completely
extirpated, representing a reduction of
approximately 64 percent of its
historical range.
The most significant threat to the
existence of the sharpnose shiner is the
modification of its habitat by reservoir
construction, irrigation and water
diversion, sedimentation, industrial and
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municipal discharges, and agricultural
activities. The current limited
distribution of the sharpnose shiner
within the Upper Brazos River Basin
makes it vulnerable to events such as
the introduction of competitive species
or prolonged drought. Other possible
threats include toxins released by
blooms of golden algae, and sand and
gravel operations in the Lower Brazos
River. The effects of these last two
possible threats may be insignificant,
but further information is necessary
before ruling them out as threats to this
species. State law does not provide
protection for the sharpnose shiner.
Because the threats are nonimminent
but of a high magnitude, a listing
priority number of 5 remains
appropriate for this species.
Smalleye shiner (Notropis buccula)—
The following summary is based on
information from our files. No new
information was provided in the
petition 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
has not been collected since 1976
downstream from the reservoir, and in
all likelihood the species is completely
extirpated from this area, representing a
reduction of approximately 64 percent
of its historical range. The most
significant threat to the existence of the
smalleye shiner is the modification of
its habitat by reservoir construction,
irrigation and water diversion,
sedimentation, industrial and municipal
discharges, and agricultural activities.
Because these threats continue to be
nonimminent and of a high magnitude,
we retain a listing priority number of 5
for 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 received on May 11, 2004. The
range of the Zuni bluehead sucker has
been reduced by over 90 percent. The
Zuni bluehead sucker currently
occupies 9 river miles in 4 areas of New
Mexico, and approximately 6 miles in
one stream of Arizona. Zuni bluehead
sucker range reduction and
fragmentation is caused by
discontinuous surface water flow,
separation of inhabited reaches by
reservoirs, and habitat degradation from
fine sediment deposition. The principal
uses of surface and ground water within
the Zuni River watershed are human
consumption, livestock, and irrigation.
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Diverting water for agricultural use is
the primary purpose of at least five
impoundments, and several other
reservoirs act as flood-control
structures. Degradation of the upper
watershed has led to increased
sedimentation, and many of the
reservoirs are now only shallow,
eutrophic ponds or wetlands with little
or no storage capacity. The
impoundments have also changed the
downstream channel morphology and
substrate composition of streams.
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.
For several years, the New Mexico
Department of Game and Fish (NMDGF)
has been the lead agency to develop a
conservation plan for Zuni bluehead
sucker. A study funded through section
6 of the ESA was initiated in 2000, and
will continue through 2005. The grant
includes funding for development and
implementation of a Zuni Bluehead
Sucker Conservation Plan and the
acquisition of additional information on
distribution, life history, and species
associations. A draft conservation plan
was completed in 2004, but the plan is
not yet final. At this time, the potential
cooperators for the conservation effort
are the Silva Family, Zuni Pueblo, U.S.
Forest Service, The Nature Conservancy,
NMDGF, and U.S. Fish and Wildlife
Service. Because of the loss of habitat,
degradation of remaining habitat, and
ongoing threats (i.e., drought and fire),
we continue to assign this subspecies a
listing priority number of 3.
Clams
Texas hornshell (Popenaias popei)—
The following summary is based on
information from our files. No new
information was provided in the
petition received on May 11, 2004.
Historically, Texas hornshell, a
freshwater mussel, occurred in the
lower Pecos River of New Mexico,
downstream throughout the Lower Rio
Grande (Brownsville, Texas) and major
tributaries in Texas, southward to the
´
´
Reo Panuco drainage of San Luis Potosı,
Mexico. Texas hornshell has declined
notably throughout its historic range
and can only be confirmed as extant in
the Black River of New Mexico and,
possibly, the Big Bend reach of the Rio
Grande in Texas. The primary threats
are ongoing habitat alterations such as
stream bank channelization,
impoundments, and diversions for
agriculture and flood control;
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contamination of water from the oil and
gas industry; alterations in the natural
riverine hydrology; and increased
sedimentation from prolonged
overgrazing and loss of native
vegetation. Thus, a listing priority
number of 2 remains appropriate for the
Texas hornshell.
Fluted kidneyshell (Ptychobranchus
subtentum)—The following summary is
based on information from our files. No
new information was provided in the
petition received on May 11, 2004. The
fluted kidneyshell is a freshwater
mussel (Unionidae) endemic to the
Cumberland and Tennessee River
systems (Cumberlandian Region) in
Alabama, Kentucky, Tennessee, and
Virginia. It requires shoal habitats in
free-flowing rivers to survive and
successfully recruit new individuals
into its populations. Habitat destruction
and alteration (e.g., impoundments,
sedimentation, and pollutants) are the
chief factors contributing to its decline.
This species has been extirpated from
numerous regional streams and is no
longer found in the State of Alabama.
The fluted kidneyshell was historically
known from at least 37 streams but is
currently restricted to no more than 14
isolated stream segments, of which only
1 (upper Clinch River) appears to be
stable and viable. Although the threats
faced by this species are significant, we
do not anticipate that they will
eliminate the species in the immediate
future (next 1–3 years). Because the
threats are high in magnitude and
nonimminent at this time, we retain a
listing priority number of 5 for this
mussel.
Neosho mucket (Lampsilis
rafinesqueana)—The following
summary is based on information from
our files. No new information was
provided in the petition received on
May 11, 2004. The Neosho mucket is a
freshwater mussel native to Arkansas,
Kansas, Missouri, and Oklahoma. The
species has been extirpated from
approximately 70 percent of its range,
and very low or no recruitment is
occurring in all of the extant
populations. Most of this extirpation has
occurred in Kansas and Oklahoma. The
Neosho mucket survives in four river
drainages; however, only two of these,
the Spring and Illinois Rivers, currently
support relatively large numbers of
individuals and thus might be selfsustaining populations. Range
restriction and population declines have
occurred in the past due to habitat
degradation attributed to
impoundments, mining, sedimentation,
and agricultural pollutants. These
threats have led to the species being
intrinsically vulnerable to extirpation.
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Although State regulations limit harvest
of this species, there is little protection
for habitat. However, populations are
stable in the Illinois River despite rapid
urbanization and development within
the watershed. Due to nonimminent
threats of a high magnitude, we retain
a listing priority number of 5 for this
species.
Alabama pearlshell (Margaritifera
marrianae)—The following summary is
based on information from our files. No
new information was provided in the
petition received on May 11, 2004. The
Alabama pearlshell inhabits shallow
riffles and pool margins of small creeks
and streams of southwest Alabama.
Only three populations of Alabama
pearlshell have been confirmed to
survive during the past 15 years. The
species has not been found at one of
these sites since 1998; observations of
increased sedimentation at this location
suggest nonpoint source pollution may
be implicated in the disappearance of
Alabama pearlshell from this stream.
The other two populations appear to be
stable and recruiting. We continue to
assign the Alabama pearlshell a listing
priority number of 2, due to the
vulnerability of small stream habitat to
nonpoint source pollution, and the
decline or loss of one of three known
populations.
Slabside pearlymussel (Lexingtonia
dolabelloidesy)—The following
summary is based on information from
our files. No new information was
provided in the petition received on
May 11, 2004. The slabside
pearlymussel is a freshwater mussel
(Unionidae) endemic to the Cumberland
and Tennessee River systems
(Cumberlandian Region) in Alabama,
Kentucky, Tennessee, and Virginia. It
requires shoal habitats in free-flowing
rivers to survive and successfully recruit
new individuals into its populations.
Habitat destruction and alteration (e.g.,
impoundments, sedimentation, and
pollutants) are the chief factors
contributing to its decline. This species
has been extirpated from numerous
regional streams and is no longer found
in the State of Kentucky. The slabside
pearlymussel was historically known
from at least 32 streams but is currently
restricted to no more than 9 isolated
stream segments. Only 3 populations
appear to be significant and viable
(Middle Fork Holston River, Paint Rock
River system, and Duck River within the
Tennessee River system). Although the
threats faced by this species are
significant, we do not anticipate that
they will eliminate the species in the
immediate future (next 1–3 years). We
continue to assign a listing priority
number of 5 to this mussel due to
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nonimminent threats of a high
magnitude.
Georgia pigtoe (Pleurobema
hanleyanum)—See above in ‘‘Summary
of Listing Priority Changes in
Candidates.’’ The above summary is
based on information contained in our
files. No new information was provided
in the petition received on May 11,
2004.
Altamaha spinymussel (Elliptio
spinosa)—The following summary is
based on information from our files. No
new information was provided in the
petition received on May 11, 2004. The
Altamaha spinymussel is a freshwater
mussel endemic to the Altamaha River
drainage of southeastern Georgia. The
historical range of the Altamaha
spinymussel was restricted to the
Coastal Plain portion of the Altamaha
River and the lower portions of its three
major tributaries, the Ohoopee,
Ocmulgee, and Oconee Rivers. The
Altamaha River is formed by the
confluence of the Ocmulgee and Oconee
rivers and lies entirely within the State
of Georgia.
Comprehensive surveys revealed that
only 14 live spinymussels have been
found and only from an isolated portion
of their range, limited to a half mile
reach of the Altamaha River. The
species appears to be extirpated from
the Ohoopee, Ocmulgee, and Oconee
Rivers, and its numbers are greatly
reduced in the Altamaha River.
Altamaha spinymussels face severe
habitat degradation from a number of
sources. Among these are threats from
sedimentation, contaminants (from
municipal wastewater treatment plants,
agricultural sources, kaolin mining and
pulp mills), and the operations of the
Edwin I. Hatch Nuclear Power Plant
within the rivers that the Altamaha
spinymussel inhabits. Water withdrawal
and drought have intensified the
impacts from contaminants, the
resulting low-flow rates provide lower
volumes of water to dilute potential
contaminants and, therefore, effectively
increase the concentrations of
contaminants in streams. In 1990, the
total amount of surface water
withdrawn from the Altamaha River
basin was 1315.88 MGD, and
development pressures continue to
grow, which will lead to increased
water withdrawals. Prolonged drought
has resulted in other negative effects to
the Altamaha spinymussel. For
instance, the drought has opened the
stream beds to all-terrain and fourwheel drive vehicle access, so mussels
that might have survived the drought
are now in danger of being crushed by
heavy vehicular traffic in the river bed
itself. These threats to the Altamaha
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spinymussel are further compounded by
its limited distribution and the low
populations sizes identified in recent
survey efforts. However, the immediacy
of these threats is not imminent. The
Altamaha River Cooperative for
Stewardship and Research has been
formed with the main objective of
identifying critical research and
conservation needs in the lower
Altamaha Basin with a particular
emphasis on relationships between
forestry practices and native biological
diversity. The Cooperative is comprised
of representatives from Plum Creek,
International Paper, The Nature
Conservancy, and the Georgia Dept. of
Natural Resources. Other stakeholders
including other industrial forestry
companies, Georgia Power, paper mills
and university researchers have also
participated in the Cooperative, but are
not formal members. As part of the
agreement the Altamaha River Scenic
Easement was established with industry
representatives to the Cooperative
contributing funds to support research
and conservation activities in the lower
Altamaha Basin. The Altamaha River
Scenic Easement is a 91.4 m (300-ft)
wide buffer strip along 45 km (28 mi) of
the Altamaha River proper comprised of
several non-contiguous parcels, most of
which occur on one but not both sides
of the river. The easement protects over
480 hectares (1200 acres) of river
shoreline and floodplain from
development, surface mining, and
logging activities. Based on
consideration of all of these conditions,
we continue to assign a listing priority
of 5 to this mussel based on
nonimminent threats of a high
magnitude.
Snails
Ogden mountainsnail (Oreohelix
peripherica wasatchensis)—The
following summary is based on
information from our files. No new
information was provided in the
petition received on May 11, 2004. The
Ogden mountain snail is known from a
single population near the mouth of
Ogden Canyon, Weber County, Utah.
The total occupied habitat is an area
approximating 100 meters (328 ft wide
by 1 kilometer (0.5 miles) long. The last
population estimates were taken in
1999, when snail numbers ranged from
approximately 9,520 in fall to 18,724 in
the spring. Based on measurement of
snail size, there appears to be little
recruitment to the population. Threats
to the colony have not substantially
changed or increased over the past year.
The habitat receives heavy recreational
use and utility roads and ORV trails are
significant barriers to dispersal and
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interconnection among subpopulations.
Based on moderate, nonimmenent
threats, we retain a listing priority
number of 9 for this subspecies.
Bonneville pondsnail (Stagnicola
bonnevillensis)—See above in
‘‘Summary of Listing Priority Changes in
Candidates.’’ The above summary is
based on information contained in our
files. No new information was provided
in the petition received on May 11,
2004.
Interrupted rocksnail (Leptoxis
foremani (= downei)—See above in
‘‘Summary of Listing Priority Changes in
Candidates.’’ The above summary is
based on information contained in our
files. No new information was provided
in the petition received on May 11,
2004.
Sisi snail (Ostodes strigatus)—The
following summary is based on
information contained in our files. No
new information was provided in the
petition received on May 11, 2004.
Belonging to the snail family, Potaridae,
the sisi snail is a ground-dwelling
species and endemic to American
Samoa. The species is now known only
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 snails.
Because the threats continue to be of a
high magnitude and are imminent, we
retain a listing priority number of 2 for
this species.
Diamond Y Spring snail
(Pseudotryonia adamantina) and
Gonzales springsnail (Tryonia
circumstriata)—The following summary
is based on information from our files.
No new information was provided in
the petition received on May 11, 2004.
The Diamond Y Spring snail and
Gonzales springsnail are small aquatic
snails endemic to Diamond Y Spring in
Pecos County, Texas. The spring and its
outflow channel are owned and
managed by The Nature Conservancy.
These snails are primarily threatened
with habitat loss due to springflow
declines from drought and from
pumping of groundwater. Additional
threats include the possibility of 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.
With imminent threats of high
magnitude, we retain a listing priority
number of 2 for this species.
Fragile tree snail (Samoana fragilis)—
The following summary is based on
information contained in our files. No
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new information was provided in the
petition received on May 11, 2004. A
tree-dwelling species, the fragile tree
snail belongs to the snail family,
Partulidae, and is endemic to the
islands of Guam and Rota (Mariana
Islands). Requiring cool and shaded
native forest habitat, the species is now
known only from a single population on
Rota. This species is currently
threatened by habitat loss and
modification and by predation from
nonnative snails. Because the threats are
of a high magnitude and are considered
imminent, we retain a listing priority
number of 2 for this species.
Gonzales springsnail (Tryonia
circumstriata)—See paragraph above
under Diamond Y Spring snail
(Pseudotryonia adamantina).
Guam tree snail (Partula radiolata)—
The following summary is based on
information contained in our files. No
new information was provided in the
petition received on May 11, 2004. A
tree-dwelling species, the Guam tree
snail belongs to the snail family,
Partulidae, and is endemic to the island
of Guam. Requiring cool and shaded
native forest habitat, the species is now
known only from eleven populations on
Guam. This species is currently
threatened by habitat loss and
modification and by predation from
nonnative snails. Because the threats
continue to be of a high magnitude and
are imminent, we retain a listing
priority number of 2 for this species.
Humped tree snail (Partula gibba)—
The following summary is based on
information contained in our files. No
new information was provided in the
petition received on May 11, 2004. A
tree-dwelling species, the humped tree
snail belongs to the snail family,
Partulidae, and was originally known
from the island of Guam and the
Commonwealth of the Northern Mariana
Islands (islands of Rota, Aguijan,
Tinian, Saipan, Anatahan, Sarigan,
Alamagan, and Pagan). Most recent
surveys revealed a total of 28
populations on the islands of Guam,
Rota, Aguijan, Tinian, Anatahan,
Sarigan, Alamagan, and Pagan.
Although still the most widelydistributed tree snail endemic in the
Mariana Islands, most of the remaining
populations are small. This species is
currently threatened by habitat loss and
modification and by predation from
nonnative snails. Because the threats are
of a high magnitude and are considered
imminent, we retain a listing priority
number of 2 for this species.
Lanai tree snail (Partulina
semicarinata)—The following summary
is based on information contained in
our files. No new information was
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provided in the petition received on
May 11, 2004. A tree-dwelling species,
Partulina semicarinata belongs to the
snail family, Achatinellidae. Endemic to
the island of Lanai, the species is
currently known from 12 populations.
This species is currently threatened by
habitat loss and modification and by
predation from nonnative snails.
Because the threats are of a high
magnitude and are imminent, we retain
a listing priority number of 2 for this
species.
Lanai tree snail (Partulina
variabilis)—The following summary is
based on information contained in our
files. No new information was provided
in the petition received on May 11,
2004. A tree-dwelling species, Partulina
variabilis belongs to the snail family,
Achatinellidae. Endemic to the island of
Lanai, the species is currently known
from 16 populations. This species is
currently threatened by habitat loss and
modification and by predation from
nonnative snails. Because the threats are
of a high magnitude and are imminent,
we retain a listing priority number of 2
for this species.
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 received on May 11,
2004. A tree-dwelling species,
Langford’s tree snail belongs to the snail
family, Partulidae, and is known from
one population on the island of Aguijan.
This species is currently threatened by
habitat loss and modification and by
predation from nonnative snails.
Because the threats are of a high
magnitude and are considered
imminent, we retain a listing priority
number of 2 for this species.
Phantom Cave snail (Cochliopa
texana) and Phantom springsnail
(Tryonia cheatumi)—The following
summary is based on information from
our files. No new information was
provided in the petition received on
May 11, 2004. The Phantom Cave snail
and Phantom springsnail are small
aquatic snails that occur in only 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 and
pumping for agricultural production.
Although the land surrounding their
habitat is owned and managed by The
Nature Conservancy, Bureau of
Reclamation, and Texas Parks and
Wildlife Department, the water needed
to maintain the habitat of both species
has declined due to a reduction in the
spring flows, possibly as a result of
private groundwater pumping in areas
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beyond that controlled by these
landowners. As an example, Phantom
Lake Spring is undergoing drying and
declining spring flows in San Solomon
Spring are also becoming evident (both
of these springs are sites of occurrence
for these springsnails). Since these
threats continue to be imminent and of
a high magnitude, we retain a priority
listing number of 2 for these species.
Tutuila tree snail (Eua zebrina)—The
following summary is based on
information contained in our files. No
new information was provided in the
petition received on May 11, 2004. A
tree-dwelling species, the Tutuila tree
snail belongs to the snail family,
Partulidae, and is endemic to American
Samoa. The species is now known only
from two populations on the island of
Tutuila. This species is currently
threatened by habitat loss and
modification and by predation from
nonnative snails. Because the threats are
of a high magnitude and are considered
imminent, we retain a listing priority
number of 2 for this species.
Chupadera springsnail (Pyrgulopsis
chupaderae)—The following summary
is based on information contained in
our files and the petition received on
November 20, 1985. See also our 12month petition finding published on
October 4, 1988 (53 FR 38969). This
aquatic species is endemic to Willow
Spring on the Willow Spring Ranch
(formerly Cienega Ranch) at the south
end of the Chupadera Mountains in
Socorro County, New Mexico. The
Chupadera springsnail has been
documented from two hillside
groundwater discharges that flow
through grazed areas among rhyolitic
gravels containing sand, mud, and
hydrophytic plants. Regional and local
groundwater depletion, springrun
dewatering, and riparian habitat
degradation represent the principal
threats. The survival and recovery of the
Chupadera springsnail is contingent
upon protection of the riparian corridor
immediately adjacent to Willow Spring
and the availability of perennial,
oxygenated flowing water within the
species’ thermal range. Due to several
factors including the extremely
localized distribution of the snail, its
occurrence only on private property, the
lack of regulatory protection of its
habitat, and the inability of land
managers to participate in its
management, the magnitude of the
threats to this species is high. There is
an imminent threat to this species
because either human-caused
disturbance (grazing of cattle, water
withdrawal, and fire) or natural
disturbance (drought or fire) could
eliminate this species in the near future.
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Therefore, due to the continuing
magnitude and imminence of threats to
this species, we retain a listing priority
number of 2 for this species.
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
45° Celsius (C) (113° Fahrenheit (F)) and
32° C (90° F)) aquatic habitat that is
approximately 300 m (984 ft) long and
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 present or
threatened destruction, modification, or
curtailment of its habitat or range by
recreational bathers in the thermal
waters is the greatest threat to the
species. The small size of their habitat
and their limited range makes them
highly susceptible to any factors that
negatively impact their habitat.
Regulatory mechanisms are beginning to
be put in place, but few actions have
been implemented to date. Based on
imminent threats of high magnitude, we
retain a listing priority number of 2 for
this species.
Gila springsnail (Pyrgulopsis gilae)—
The following summary is based on
information contained in our files and
the petition received on November 20,
1985. Also see our 12-month petition
finding published on October 4, 1988
(53 FR 38969). The Gila springsnail is
an aquatic species known from 13
populations in New Mexico. The longterm persistence of the Gila springsnail
is contingent upon protection of the
riparian corridor immediately adjacent
to springhead and springrun habitats
(habitat at the springhead and along the
watercourse running from the
springhead), thereby ensuring the
maintenance of perennial, oxygenated
flowing water within the species’
required thermal range. Sites on both
private and Federal lands are subject to
levels of recreational use and livestock
grazing that negatively affect this
species, thus placing the longterm
survival of the Gila springsnail at risk.
Natural events such as drought, forest
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fire, sedimentation, and flooding;
wetland habitat degradation by
recreational bathing in thermal springs;
and poor watershed management
practices represent the primary threats
to the Gila springsnail. Fire suppression
activities and fire retardant chemicals
have potentially deleterious effects on
this species. Because several of the
springs occur on Forest Service land,
management options for the protection
of the snail should be possible.
However, randomly occurring events,
especially fire and drought, could have
a major impact on the species. Moderate
use by recreationalists and livestock is
ongoing. If these uses remain at current
or lower levels, they will not pose an
imminent threat to the species. Of
greater concern is the current drought
that could impact spring discharge and
which increases the potential for fire.
Significant fires have occurred in the
Gila National Forest, and subsequent
floods and ash flows have severely
impacted aquatic life in streams. If the
drought continues or worsens, the
imminence of threat (decreased
discharge, fire) will increase. Based on
these nonimminent threats that are
currently of a low magnitude, we retain
a listing priority number of 11 for this
species.
Huachuca springsnail (Pyrgulopsis
thompsoni)—The following summary is
based on information from our files. No
new information was provided in the
petition received on May 11, 2004. The
Huachuca springsnail inhabits 13
springs and cienegas at elevations of
4,500 to 7,200 feet in southeastern
Arizona (11 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. Potential threats include habitat
modification, wildfire, cattle grazing,
and groundwater pumping. Recent
communication with personnel from
Fort Huachuca indicates they are in the
process of evaluating the status of
species on Department of Defense lands
and developing conservation strategies;
this may result in a reduction or
elimination of threats in the future.
Currently, however, due to the high
magnitude and nonimminent threats,
we continue to assign a listing priority
number of 5 for this species.
New Mexico springsnail (Pyrgulopsis
thermalis)—The following summary is
based on information contained in our
files and the petition received on
November 20, 1985. Also see our 12month petition finding published on
October 4, 1988 (53 FR 38969). The New
Mexico springsnail is an aquatic species
known from only two separate
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populations associated with a series of
spring-brook systems along the Gila
River in the Gila National Forest in
Grant County, New Mexico. The
longterm persistence of the New Mexico
springsnail is contingent upon
protection of the riparian corridor
immediately adjacent to springhead and
springrun habitats, thereby ensuring the
maintenance of perennial, oxygenated
flowing water within the species’
required thermal range.
While the New Mexico springsnail
populations may be stable, the sites
inhabited by the species are subject to
levels of recreational use and livestock
grazing that negatively affect this
species. Wetland habitat degradation by
recreational use and overgrazing in or
near the thermal springs and/or
inadequate watershed management
practices represent the primary threats
to the New Mexico springsnail.
Moderate use by recreationalists and
livestock is ongoing. If these uses
remain at the current or lower levels,
they will not pose an imminent threat
to the species. Of greater concern is the
current drought, which could impact
spring discharge and increases the
potential for fire. Significant fires have
occurred in the Gila National Forest and
subsequent floods and ash flows have
severely impacted aquatic life in
streams. If the drought continues or
worsens, the imminence of threat
(decreased discharge, fire) will increase.
Based on these nonimminent threats of
a low magnitude, we retain a listing
priority number of 11 for this
springsnail.
Page springsnail (Pyrgulopsis
morrisoni)—The following summary is
based on information from 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 1.5-kilometer
(0.93-mile) stretch along the west side of
Oak Creek around the community of
Page Springs, Yavapai County, Arizona.
Many of the springs where the
springsnail occurs have been subjected
to some level of modification for
domestic, agricultural, ranching, fish
hatchery, and recreational activities.
Arizona Game and Fish Department
(AGFD) management plans for the
Bubbling Ponds and Page Springs fish
hatcheries include commitments to
replace lost habitat and to monitor
remaining populations of invertebrates
such as the Page springsnail. Based on
recent survey data, it appears that the
Page springsnail is abundant within its
habitats and is more widely distributed
than previously known. Monitoring by
AGFD and Service biologists no longer
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entails snail removal, which appears to
have had a temporary positive impact
on population numbers. The threat of
ground water withdrawal is not
considered imminent because recent
studies indicate that the groundwater
system of the Verde Valley has not yet
been affected by development, and base
flow in the Verde River Valley has
remained virtually unchanged since
1915. Because these threats are
nonimminent but continue to be of a
high magnitude, we retain a listing
priority number of 5 for this species.
Three Forks springsnail (Pyrgulopsis
trivialis)—The following summary is
based on information from our files. No
new information was provided in the
petition received on May 11, 2004. The
Three Forks springsnail is an endemic
species with distribution limited to the
Three Forks Springs and Boneyard
Springs spring complexes in the North
Fork East Fork Black River Watershed of
east-central Arizona. The springsnail is
known from free-flowing spring heads,
concrete boxed spring heads, spring
runs, and spring seepage at these sites.
The primary threats include habitat
modification from recreational
activities, damage from elk wallowing,
and predation from nonnative crayfish.
The Arizona Game and Fish Department
currently maintains an active
monitoring program for the Three Forks
springsnail in cooperation with the Fish
and Wildlife Service and Forest Service.
This program includes population
monitoring, habitat sampling, and
removal of nonnative predatory
crayfish. However, in the absence of a
management strategy to effectively
address the threat from both elk and
crayfish in a longterm fashion, we
believe the immediacy of threats to be
imminent. Therefore, we retain a listing
priority number of 2 for the Three Forks
springsnail.
Newcomb’s tree snail (Newcombia
cumingi)—See above in ‘‘Summary of
Listing Priority Changes in Candidates.’’
The above summary is based on
information contained in our files. No
new information was provided in the
petition received on May 11, 2004.
Insects
Warm Springs Zaitzevian riffle beetle
(*COM044*Zaitzevia thermae)—The
following summary is based on
information from our files. No new
information was provided in the
petition received on May 11, 2004. The
Warm Springs Zaitzevian riffle beetle is
a small, flightless beetle. It is globally
endemic to a single, small warm spring
along a creek in southwestern Montana.
A concrete box has been constructed to
protect the spring from contaminants
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that may enter the adjacent creek. As a
result, the beetle habitat is protected
from contamination or trampling,
although the possibility for breaching of
the cement box exists if extreme events
were to occur. The most recent survey
indicates the beetle is abundant both
within the cement box and in seeps
outside the box. Because of its naturally
limited distribution, the species is
vulnerable to randomly occurring
natural and human-caused events.
However, because of the protection of
the habitat, the magnitude of threats is
low and threats are nonimminent,
resulting in our retention of a listing
priority number of 11 for this species.
Wekiu bug (Nysius wekiuicola)—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
Wekiu bug belongs to the true bug
family, Lygaeidae, and is endemic to the
island of Hawaii. Originally and
currently known from one widespread
population on the summit of Mauna
Kea, the species feeds upon other insect
species that are blown to the summit of
this large volcano. This species is
currently threatened by competition
with and predation by nonnative
arthropods, impacts from recreational
and astronomy activities on the summit,
and loss of habitat from astronomy
development. Because the threats are of
a high magnitude and are considered
imminent, we retain a listing priority
number of 2 for this species.
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 received on May 11, 2004. The
Mariana eight spot butterfly is a
nymphalid butterfly species which
feeds upon two host plants, Procris
pedunculata and Elatostema calcareum.
Endemic to the island of Guam and the
Mariana Islands, the species is now
known from ten populations on Guam.
This species is currently threatened by
predation and parasitism from
nonnative species and impacts to its
host plants by browsing ungulates.
Because the threats are of a high
magnitude and are considered
imminent, we retain a listing priority
number 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 received on May 11,
2004. The Mariana wandering butterfly
is a nymphalid butterfly species which
feeds upon a single host plant species,
Maytenus thompsonii. Originally known
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from and endemic to the islands of
Guam and Rota (of the Mariana Islands),
the species is now known only from one
population on Rota. This species is
currently threatened by predation and
parasitism from nonnative species, and
impacts to its host plants by browsing
ungulates. Because the threats continue
to be of a high magnitude and are
considered imminent, we retain a listing
priority number of 2 for this species.
Miami blue butterfly (Cyclargus
thomasi bethunebakeri)—See above in
‘‘Summary of New Candidates.’’ The
above summary is based on information
contained in our files and in the petition
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 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. The Owen Spring Branch
population occurs within Sequatchie
Cave Park, which is a Class II NaturalScientific State Natural Area, thus
providing statutory protection from
collection for the population in Owen
Spring Branch. Estimated population
sizes are 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. Threats to the species include
siltation; agricultural, municipal, and
industrial chemical runoff (both direct
and from subsurface flows); vandalism,
and pollution from trash thrown into
the springs. This species is vulnerable to
extinction due to its restricted
distribution and small population sizes.
These threats are gradual and/or not
necessarily imminent but are of a high
magnitude; therefore, we retain a listing
priority number of 5 for this species.
Inquirer cave beetle
(Pseudanophthalmus inquistor Barr),
Beaver cave beetle (Pseudanophthalmus
major Krekeler), Tatum Cave beetle
(Pseudanophthalmus parvus Krekeler),
and Louisville cave beetle
(Pseudanophthalmus troglodytes
Krekeler)—The following summary is
based on information contained in our
files. No new information was provided
in the petition received on May 11,
2004. Cave beetles in the genus
Pseudanophthalmus are fairly small,
eyeless, reddish-brown insects. The
limestone caves in which these cave
beetles are found provide a unique and
fragile environment that supports a
variety of species that have evolved to
survive and reproduce under the
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demanding conditions found in cave
ecosystems.
The inquirer cave beetle was
described in 1980, from specimens
collected in Sheals’s Cave, Clay County,
Tennessee. The species is not known
from any other caves. During a 1997
survey of the cave, three inquirer cave
beetles were observed. The Beaver Cave
beetle was described in 1973, from 3
specimens collected from Beaver Cave,
Harrison County, Kentucky. No
additional caves that could provide
habitat for the Beaver Cave beetle were
found during a 1996 survey of Beaver
Cave and the surrounding area. One
specimen of the species was observed in
Beaver Cave during the 1996 survey.
The Tatum Cave beetle was described in
1973 from material collected from
Tatum Cave, Marion County, Kentucky.
No individuals were observed during
surveys in 1980 and in 1996. The
species has not been observed in Tatum
Cave since 1965. There are no other
known caves in the vicinity of Tatum
Cave that could support the species. The
Louisville cave beetle was described in
1973 from specimens collected from
Oxmoor Cave, Jefferson County,
Kentucky. During 1994, surveys of other
caves that could potentially support the
species were conducted and the species
was found in only one additional cave
(Eleven Jones Cave).
All of these cave beetles are currently
known from only one or two caves.
Their limited distributions make them
vulnerable to isolated events that would
only have a minimal effect on the more
wide-ranging members of the genus.
Events such as toxic chemical spills,
discharges of large amounts of polluted
water, closure of entrances, alteration of
entrances, or the creation of new
entrances can have serious adverse
impacts on these cave beetles and could
result in their extinction. No formal
protection is currently provided to these
species. The threats faced by these
species are significant; however, it is not
anticipated that they will be subject to
these threats in the immediate future
(next 1–2 years). Therefore, we retain a
listing priority of 5 for these cave
beetles.
Clifton Cave beetle
(Pseudanophthalmus caecus Krekeler),
Lesser Adams Cave beetle
(Pseudanophthalmus cataryctos
Krekeler), Greater Adams Cave beetle
(Pseudanophthalmus pholeter
Krekeler), and Icebox Cave beetle
(Pseudanophthalmus frigidus Barr)—
The following summary is based on
information contained in our files. No
new information was provided in the
petition received on May 11, 2004. Cave
beetles in the genus
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Pseudanophthalmus are fairly small,
eyeless, reddish-brown insects. The
limestone caves in which these cave
beetles are 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 Clifton Cave beetle was described
in 1973 by Krekeler based upon material
collected in 1963. The cave supporting
this species is near Versailles, Woodford
County, Kentucky. Soon after the
species was first collected, the entrance
to the cave was enclosed due to road
construction. Other caves in the vicinity
of Clifton Cave were surveyed for the
species in 1995–1996. Most contained
other species of Pseudanophthalmus,
but only one additional site was found
for the Clifton Cave beetle. Four
specimens were found in a very small,
30 foot (9 meters) long cave about 1 mile
(1.61 kilometers) from Clifton Cave. It
can not be determined at this time if the
species still occurs in Clifton Cave or if
the species has been extirpated from its
type locality by the closure of the cave
entrance.
The Lesser Adams Cave beetle was
described in 1973 based upon material
collected from Adams Cave, Madison
County, Kentucky. This cave also
supports the Greater Adams Cave beetle,
which also was described in 1973.
During a 1995 visit to the cave, one of
the original collectors observed one
specimen of the Lesser Adams Cave
beetle, but the Greater Adams Cave
beetle was not observed. In 2002, one
lesser Adams Cave beetle and two
greater Adams Cave beetles were found
during a biological survey conducted by
the Service and the Kentucky State
Nature Preserves Commission. There are
no other caves in the vicinity of Adams
Cave, and this species has not been
found at any other locations. A gate to
control access to the cave was
constructed in 2002. On March 1, 2005,
a Candidate Conservation Agreement
was signed which will provide for longterm protection for Adams Cave and the
species that depend upon it.
Icebox Cave beetle was described in
1981 based upon two specimens
collected from Icebox Cave, Bell County,
Kentucky. Despite searches of caves in
the vicinity of this cave and several later
visits to Icebox Cave, no additional
specimens of Icebox Cave beetle have
been found.
All of these cave beetles are currently
known from only one or two caves.
Their limited distributions make them
vulnerable to isolated events that would
only have a minimal effect on the more
wide-ranging members of the genus.
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Events such as toxic chemical spills,
discharges of large amounts of polluted
water, closure of entrances, alteration of
entrances, or the creation of new
entrances can have serious adverse
impacts on these cave beetles and could
result in their extinction. No formal
protection is currently provided to these
species. The threats faced by these
species are significant; however, it is not
anticipated that they will be subject to
these threats in the immediate future
(next 1–2 years). We retain a listing
priority number of 5 for these species.
Surprising cave beetle
(Pseudanophthalmus inexpectatus
Barr)—The following summary is based
on information contained in our files.
No new information was provided in
the petition received on May 11, 2004.
Cave beetles in the genus
Pseudanophthalmus are fairly small,
eyeless, reddish-brown insects. The
limestone caves in which these cave
beetles are 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 surprising cave beetle
was described from specimens collected
in the historic section of Mammoth Cave
and White Cave, Mammoth Cave
National Park (MCNP), Edmonston
County, Kentucky. Subsequent to these
original discoveries, the species was
also found in MCNP’s Great Onyx Cave.
Recently, an additional population has
been discovered in a cave some distance
from the previously known sites. Its
limited distribution makes this species
vulnerable to isolated events that would
only have a minimal effect on the more
wide-ranging members of the genus.
Events such as toxic chemical spills,
discharges of large amounts of polluted
water, closure of entrances, alteration of
entrances, or the creation of new
entrances can have serious adverse
impacts on this species and could result
in its extinction. The magnitude of the
threat to the surprising cave beetle is
reduced because of its location on
Federal land and the formal
commitment through a Candidate
Conservation Agreement between
MCNP and the Service to protect the
species. Therefore we retain a listing
priority number of 11 for this species.
Taylor’s (Whulge, Edith’s)
checkerspot butterfly (Euphydryas
editha taylori)—The following summary
is based on information from our files
and in the petition received on
December 11, 2002. Historically,
Taylor’s checkerspot butterflies were
known from 70 locations: 23 in British
Columbia, 34 in Washington, and 13 in
Oregon. By spring 2004, only 14
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populations, with a total of about 2,000
individuals, were known: 12 in
Washington and 2 in the Willamette
Valley of Oregon. The species may be
extirpated in British Columbia. Threats
include degradation and destruction of
native grasslands through conversion to
agriculture; residential development
and commercial development;
encroachment by nonnative plants;
succession from grasslands to native
shrubs and trees; and fire. The
application of Bacillus thuringiensis var.
kurstaki for Asian gypsy moth control
likely contributed to extirpations of the
subspecies at three locations in Pierce
County, Washington. The magnitude of
threats is high because of the extremely
small size of remaining populations and
reduction in distribution from the
historical range. Sizes and locations of
the populations shift from year to year.
The ecosystem on which this subspecies
depends requires annual management to
maintain grassland habitat. Threats are
imminent because any of the numerous
threats could occur at any time. We
retain a listing priority number of 3 for
Taylor’s checkerspot.
Blackline Hawaiian damselfly
(Megalagrion nigrohamatum
nigrolineatum)—The following
summary is based on information
contained in our files. No new
information was provided in the
petition received on May 11, 2004.
Megalagrion nigrohamatum
nigrolineatum is a stream-dwelling
damselfly species endemic to the island
of Oahu, Hawaii. Once known from
throughout Oahu, the species is now
restricted to 11 populations within the
windward Koolau Mountains. This
species is threatened by predation from
nonnative aquatic species such as fish
and predacious insects and habitat loss
through dewatering of streams. Because
the threats are of a moderate magnitude
and are considered imminent, we retain
a listing priority number of 9 for this
subspecies.
Crimson Hawaiian damselfly
(Megalagrion leptodemas)—The
following summary is based on
information contained in our files. No
new information was provided in the
petition received on May 11, 2004.
Megalagrion leptodemas is a streamdwelling damselfly species endemic to
the island of Oahu, Hawaii. Once
known from throughout Oahu, the
species is now restricted to four
populations. This species is threatened
by predation from nonnative aquatic
species such as fish and predacious
insects, and habitat loss through
dewatering of streams. Because the
threats continue to be of a high
magnitude and are considered
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imminent, we retain a listing priority
number of 2 for this species.
Flying earwig Hawaiian damselfly
(Megalagrion nesiotes)—The following
summary is based on information
contained in our files. No new
information was provided in the
petition received on May 11, 2004.
Megalagrion nesiotes is a terrestrial or
semi-terrestrial damselfly species
endemic to the islands of Hawaii and
Maui, Hawaii. Despite extensive surveys
to locate extant populations, the species
is now known to be restricted to a single
population in windward east Maui. This
species is threatened by predation from
ants and other nonnative arthropods,
and habitat loss due to disturbance by
feral ungulates. Because the threats
continue to be of a high magnitude and
are considered imminent, we retain a
listing priority number of 2 for this
species.
Oceanic Hawaiian damselfly
(Megalagrion oceanicum)—The
following summary is based on
information contained in our files. No
new information was provided in the
petition received on May 11, 2004.
Megalagrion oceanicum is a streamdwelling damselfly species endemic to
the island of Oahu, Hawaii. Once
known from throughout Oahu, the
species is now restricted to seven
populations within the windward
Koolau Mountains. This species is
threatened by predation from nonnative
aquatic species such as fish and
predacious insects, and habitat loss
through dewatering of streams. Because
the threats continue to be of a high
magnitude and are considered
imminent, we retain a listing priority
number of 2 for this species.
Orangeblack Hawaiian damselfly
(Megalagrion xanthomelas)—The
following summary is based on
information contained in our files. No
new information was provided in the
petition received on May 11, 2004.
Megalagrion xanthomelas is a streamdwelling damselfly species endemic to
the Hawaiian Islands of Kauai, Oahu,
Molokai, Maui, Lanai, and Hawaii. The
species is now restricted to 16
populations on the islands of Oahu,
Molokai, Lanai, and Hawaii. This
species is threatened by predation from
nonnative aquatic species such as fish
and predacious insects and habitat loss
through dewatering of streams. Because
the threats continue to be of a moderate
magnitude and are considered
imminent, we retain a listing priority
number of 8 for this species.
Pacific Hawaiian damselfly
(Megalagrion pacificum)—The
following summary is based on
information contained in our files. No
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new information was provided in the
petition received on May 11, 2004.
Megalagrion pacificum is a slow-moving
stream-, pool-, and pond-dwelling
damselfly species endemic to the
Hawaiian Islands of Kauai, Oahu,
Molokai, Maui, Lanai, and Hawaii. The
species is now restricted to seven
populations on the islands of Maui and
Molokai. This species is threatened by
predation from nonnative aquatic
species such as fish and predacious
insects, and habitat loss through
dewatering of streams. Because the
threats continue to be of a high
magnitude and are considered
imminent, we retain a listing priority
number of 2 for this species.
Poolanui gall fly (Phaeogramma
sp.)—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 poolanui gall fly belongs to the fly
family, Tephritidae, and forms galls on
its host plant, Bidens cosmoides, upon
which it also breeds and feeds. The fly
is endemic to the Hawaiian Island of
Kauai, where it is currently known from
seven populations. This species is
threatened throughout its limited range
by the loss and modification of its host
plant’s habitat through the uncontrolled
growth of nonnative plants.
Additionally, the species is highly
threatened by parasitism by nonnative
wasp species. However, threats to the
Poolanui gall fly from nonnative weeds
and parasitoids are considered
nonimminent because they are not
ongoing. Because the threats continue to
be of a high magnitude and are
considered nonimminent, we retain a
listing priority number of 5 for this
species.
Picture wing fly (Drosophila
attigua)—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 picture wing fly belongs to
the fly family, Drosophilidae, and feeds
and breeds upon a single host plant,
Cheirodendron sp. The fly is endemic to
the Hawaiian Island of Kauai, where it
is currently known from two
populations. This species is currently
threatened by loss and modification of
its host plant’s habitat by browsing
ungulates and through the uncontrolled
growth of nonnative plants.
Additionally, the species is threatened
by predation and parasitism by
nonnative insect species. Because the
threats continue to be of a high
magnitude and are considered
imminent, we retain a listing priority
number of 2 for this species.
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Picture wing fly (Drosophila
digressa)—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 picture wing fly belongs to
the fly family, Drosophilidae, and feeds
and breeds upon a single host plant,
Charpentiera sp. The fly is endemic to
the island of Hawaii, where it is
currently known from three
populations. This species is currently
threatened by loss and modification of
its host plant’s habitat by browsing
ungulates and through the uncontrolled
growth of nonnative plants.
Additionally, the species is threatened
by predation and parasitism by
nonnative insect species. Because the
threats continue to be of a high
magnitude and are considered
imminent, we retain a listing priority
number of 2 for this species.
Stephan’s riffle beetle (Heterelmis
stephani)—The following summary is
based on information from 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 Bog Spring and
Sylvester Spring in Madera Canyon,
within the Coronado National Forest.
These springs are typical isolated, midelevation, permanently saturated,
spring-fed aquatic climax communities
´
commonly referred to as cienegas.
Threats are largely from habitat
modification. However, because the
Forest Service has no current plans to
modify remaining habitat, the threats
are not imminent. Due to the continued
high magnitude of nonimminent threats,
we retain a listing priority number of 5
for 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 States with
extant locations. The species is
threatened by conversion of its native
prairie habitat for agricultural purposes,
overgrazing, invasive species, gravel
mining, and inbreeding. In addition,
prairie is converted to shrubland or
forest without periodic fire, grazing, or
mowing; thus, the species is also
threatened at sites where such
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disturbance is not allowed. Although
the species is listed as threatened by the
State of Minnesota, this designation
lacks the habitat protections needed for
long-term conservation. The species is
also listed as endangered by the
province of Manitoba. The U.S. Fish and
Wildlife Service, other agencies, and
private organizations (e.g., The Nature
Conservancy) protect and manage some
Dakota skipper sites; although proper
management is always necessary to
ensure its persistence, it is generally
secure at these sites. The species is also
secure at some sites where private
landowners manage native prairie in
ways that conserve the Dakota skipper.
Therefore, the threats to the species
continue to be relatively moderate and
generally nonimminent, although some
sites are imminently threatened.
Therefore, we retain a listing priority
number of 11 for this species.
Mardon skipper (Polites mardon)—
The following summary is based on
information contained in our files and
the petition 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 locations:
south Puget Sound region, southern
Washington Cascades, Siskiyou
Mountains of southern Oregon, and
coastal California. The Mardon skipper
spends its entire life cycle in one
location, and its dispersal ability is
probably limited. Threats include
habitat loss and degradation due to
development, overgrazing, use of
herbicides and pesticides,
encroachment of nonnative and native
vegetation, succession from grassland to
forest, fire suppression; direct loss of
individuals due to fire; recreational
activities; insect collecting; and random,
naturally occurring events. Limited
dispersal ability limits the likelihood of
recolonization once a population is lost.
The magnitude of threats is high
because of the small population sizes
and disjunct distributions that limit
dispersal. Loss of any of the populations
could threaten the continued existence
of the species. Threats are nonimminent
because the number of documented
locations for the species has increased
from less than 10 in 1998 to greater than
50 rangewide in 2004. However, only 10
locations have more than 50
individuals. We retain a listing priority
number of 5 for the Mardon skipper.
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
received on April 21, 1994. The Coral
Pink Sand Dunes tiger beetle is known
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to occur only at Coral Pink Sand Dunes,
about 7 miles west of Kanab, Kane
County, in south-central Utah. It is
restricted mostly to a small part of the
approximately 13-kilometer (8-mile)
long dune field, situated at an elevation
of about 1,820 m (6,000 ft). The beetle’s
habitat is being adversely affected by
ongoing recreational off-road vehicle
(ORV) use. The ORV activity is
destroying and degrading the beetle’s
habitat, especially the interdunal swales
used by the larval population. Having
the greatest abundance of suitable prey
species, the interdunal swales are the
most biologically productive areas in
this ecosystem. The continued survival
of the beetle depends on the
preservation of its habitat at its only
breeding site and probably requires the
establishment or reestablishment of
additional reproductive subpopulations
in other suitable habitat sites. The
beetle’s population is also vulnerable to
overcollecting by professional and
hobby tiger beetle collectors, although
quantification of this threat is difficult
without continuous monitoring of the
beetle’s population. The recreational
ORV use threat is currently managed by
active measures taken by both the Utah
Department of Parks and Recreation and
the BLM, which reduces the threat from
high to moderate. The subspecies
population is still at low levels and has
only recently improved. Based on
continued imminent threats of a low to
moderate magnitude, we retain a listing
priority number of 9 for this subspecies.
Highlands tiger beetle (Cicindela
highlandensis)—The following
summary is based on information in our
files. No new information was provided
in the petition received on May 11,
2004. This is a small, relatively plain
tiger beetle. It is narrowly distributed
and is restricted to areas of bare sand
within upland oak scrub and longleaf
pine vegetation on the ancient sand
dunes of the Lake Wales Ridge in Polk
and Highlands Counties, Florida. The
Highlands tiger beetle has been found at
40 sites from near Haines City south to
Josephine Creek. It is found near (and
possibly in) the Snell Creek unit of Lake
Wales Ridge National Wildlife Refuge
(LWRNWR), in the Allen David
Broussard Catfish Creek Preserve
(Florida State Parks), The Nature
Conservancy’s Tiger Creek Preserve, the
Lake Wales Ridge State Forest’s Walkin-Water tract Lake Weohyakapka and
the west side of Lake Arbuckle (Lake
Wales Ridge State Forest), Carter Creek
(Lake Wales Ridge Wildlife and
Environmental Area, Florida Fish and
Wildlife Conservation Commission), the
Flamingo Villas tract of LWRNWR, to
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the vicinity of Josephine Creek (tracts
managed by the Southwest Florida
Water Management District and the
Lake Wales Ridge Wildlife and
Environmental Area). A large portion of
the good Highlands tiger beetle sites are
protected and managers are
implementing prescribed fire programs
that should restore tiger beetle habitat in
some areas. Lack of fire to create open
sand is a serious threat to this species.
Because this is a very narrowly
distributed species with exacting habitat
requirements and small populations, the
magnitude of threats continues to be
high. Therefore, we retain a listing
priority number of 5 for the Highlands
tiger beetle.
Arachnids
Warton’s cave meshweaver (Cicurina
wartoni)—The following summary is
based on information from our files. No
new information was provided in the
petition received on May 11, 2004.
Warton’s cave meshweaver occurs in
one cave in northeastern Travis County,
Texas. Competition and predation from
imported red fire ants, runoff from roads
and homesites, and unauthorized
human activities are the primary threats
to this karst invertebrate. These
activities are imminent because they are
known to occur or are highly likely
around the only cave known to be
occupied by the species. Because of the
single location, threats to the species
from fire ants, pollution from nearby
activities, and unauthorized activities
near the feature, we consider the threat
magnitude to be high. Because these
threats continue to be imminent and are
of a high magnitude, we retain a listing
priority number of 2 for this species.
Crustaceans
Anchialine pool shrimp (Antecaridina
lauensis)—The following summary is
based on information contained in our
files. No new information was provided
in the petition received on May 11,
2004. Antecaridina lauensis is an
anchialine pool-inhabiting species of
shrimp belonging to the family, Atyidae.
This species has a disjunct, Indo-Pacific
distribution and is indigenous to the
Hawaiian Islands. In Hawaii, the species
is currently known from two
populations on the island of Maui and
two populations on the island of
Hawaii. The primary threats to this
species are habitat loss and predation
from nonnative fish species. These
threats are ongoing. Because the threats
continue to be of a high magnitude and
are imminent, we retain a listing
priority number of 2 for this species.
Anchialine pool shrimp (Calliasmata
pholidota)—The following summary is
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based on information contained in our
files. No new information was provided
in the petition received on May 11,
2004. Calliasmata pholidota is an
anchialine pool-inhabiting species of
shrimp belonging to the family,
Alpheidae. This species has a disjunct,
Indo-Pacific distribution and is
indigenous to the Hawaiian Islands. In
Hawaii, the species is currently known
from six populations on the island of
Maui and one population on the island
of Hawaii. The primary threats to this
species are habitat loss and predation
from nonnative fish species; these
threats are ongoing. Because the threats
continue to be of a high magnitude and
are imminent, we retain a listing
priority number of 2 for this species.
Anchialine pool shrimp (Metabetaeus
lohena)—The following summary is
based on information contained in our
files. No new information was provided
in the petition 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 Maui and Hawaii. The primary
threats to this species are habitat loss
and predation from nonnative fish
species; these threats are ongoing.
Because the threats continue to be of a
high magnitude and are imminent, we
retain a listing priority number of 2 for
this species.
Anchialine pool shrimp
(Palaemonella burnsi)—The following
summary is based on information
contained in our files. No new
information was provided in the
petition 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 habitat loss and predation
from nonnative fish species; these
threats are ongoing. Because the threats
continue to be of a high magnitude and
are imminent, we retain a listing
priority number of 2 for this species.
Anchialine pool shrimp (Procaris
hawaiana)—The following summary is
based on information contained in our
files. No new information was provided
in the petition 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
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island of Maui and one population on
the island of Hawaii. The primary
threats to this species are habitat loss
and predation from nonnative fish
species; these threats are ongoing.
Because the threats continue to be of a
high magnitude and are imminent, we
retain a listing priority number of 2 for
this species.
Anchialine pool shrimp (Vetericaris
chaceorum)—See above in ‘‘Summary of
Listing Priority Changes in Candidates.’’
The above summary is based on
information contained in our files. No
new information was provided in the
petition received on May 11, 2004.
Troglobitic groundwater shrimp
(Typhlatya monae)—The following
summary is based on information from
our files. No new information was
provided in the petition received on
May 11, 2004. Typhlatya monae is a
subterranean small shrimp known from
Puerto Rico, Barbuda, and Dominican
Republic. Although in Puerto Rico it
was previously found at Mona Island,
currently the species is known from
´
only three caves within the Guanica
Commonwealth Forest in the
´
municipalities of Guanica, Yauco, and
Guayanilla. The species may still be
found in the reef deposit aquifers in
Mona Island that have not yet been
surveyed. Little is known concerning
the status of Typhlatya monae in either
Barbuda or Dominican Republic.
Changes in groundwater quality,
collection, predation, development
projects, and its limited distribution and
population numbers threaten this
species. These threats are not imminent.
Although the known populations are
found within protected lands, the
threats are of a high magnitude due to
the limited distribution of the species.
We retain a listing priority number of 5
for this species.
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 received on
May 11, 2004. Abronia alpina is a small,
generally glandular, deeply-rooted
perennial herb, 2.5 to 15.2 centimeters
(1 to 6 inches) across forming compact
mats found on gravel meadow margins
between lodgepole pine forest and
sagebrush scrub communities at an
elevation between 2,621 to 2,652 meters
(m) (8,600 to 8,700 feet (ft)). 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.
Population estimates from 1985 through
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1994 ranged 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.
Threats include encroachment of
lodgepole pine into the meadow habitat,
changes in hydrology of the meadow,
and trampling of habitat due to
recreational activities. Disease is not
known to be a factor for the species at
this time; however, gopher activity may
result in significant destruction of
Abronia alpina through collection or
burrowing activities. Significant
trampling of Abronia alpina
subpopulations by cattle has occurred in
the past; however, in 2001, the U.S.
Forest Service (USFS) made the
decision to discontinue grazing on the
Templeton allotment, which includes
Ramshaw Meadow, for a period of 10
years. In January 2004, the USFS
determined, as a result of the Sierra
Nevada Forest Plan Amendment and the
final supplemental environmental
impact statement (FSEIS), that livestock
grazing posed a threat to this species.
However, the FSEIS notes that future
decisions to allow livestock grazing will
consider effects to this species and this
may require updating the 2001 draft
Conservation Agreement which the
USFS has been using as their
management strategy.
Due to the extremely limited
geographic range of the species,
biological factors such as disease, pest
outbreak, and random chance events
associated with the highly variable
climate can pose a serious threat to the
species. Abronia alpina apparently is
slow to recover from disturbance
because of reproductive and dispersal
limitations, short life span, and high
annual fluctuation in population
numbers. Nonadaptive forces such as
inbreeding depression may also threaten
the species when combined with the
fragmented distribution of the species.
We conclude that the magnitude of
threats to Abronia alpina continue to be
moderate, rather than high, because 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 also conclude these threats
continue to be nonimminent, since the
threats are not expected to change in the
foreseeable future. Therefore, we retain
a listing priority of 11 for this species.
Aliciella (Gilia) cespitosa
(Wonderland alice-flower)—The
following summary is based on
information from our files. No new
information was provided in the
petition received on May 11, 2004. The
Wonderland alice-flower or Rabbit
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Valley gilia is a plant within the
Polemoniaceae or Phlox family found in
Wayne County, Utah. The species is
primarily associated with sand-filled
pockets and crevices of Navajo
sandstone on detrital slopes produced
by mechanical weathering or erosion of
rock in pinyon-juniper/mountain
mahogany communities between 5,200
and 9,000 feet in elevation. Surveys
from 2000 to 2003 resulted in estimated
numbers of 27,000 individual plants.
Current threats include recreational
trails; off-road vehicle use; collection by
rock garden enthusiasts; livestock
trampling; and low natural recruitment.
Though localized threats exist, the
magnitude of threats is low to moderate
with none of them considered
imminent, as the majority of sites are
not easily accessible. Based on these
factors, we retain a listing priority of 11
for this species.
Arabis georgiana (Georgia
rockcress)—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 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 a total of 18
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, more than outright
habitat destruction, is the most serious
threat to this species’ continued
existence. 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. Eight populations are currently
or potentially threatened by the
presence of exotics. The Natural
Heritage programs in Alabama and
Georgia have initiated plans for exotic
control at several populations;
nonnative plant removal has taken place
at several sites. The magnitudes of
threats to this species continue to be
moderate to low due to the number of
populations (18) across multiple
counties in 2 states. The primary threat
to the species of invading exotics is
nonimminent. Thus, we retain a listing
priority number of 11 for this species.
Argythamnia blodgettii (Blodgett’s
silverbush)—The following summary is
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based on information in our files. No
new information was provided in the
petition received on May 11, 2004. This
member of the spurge family is
currently known from tropical
pinelands on limestone rock (pine
rocklands) at 18 sites in Miami-Dade
and Monroe Counties in Florida. Its
range extends from Coral Gables (near
central Miami) and southern MiamiDade County westward to southwestern
Long Pine Key, a pineland within
Everglades National Park. It is also
present in the lower Florida Keys from
Windley Key southwest to Big Pine Key.
Blodgett’s silverbush is protected at
Biscayne and Everglades National Parks,
the Florida Keys Wildlife and
Environmental Area, six Miami-Dade
County conservation areas, Lignumvitae
Key Botanical State Park, Long Key
State Park, National Key Deer Refuge,
Pine Ridge Sanctuary (private), and
Windley Key Fossil Reef Geological
State Park. It is also present at Florida
Power and Light’s Everglades Mitigation
Bank. The species could be present at
John Pennekamp Coral Reef State Park.
The largest population, up to 10,000
plants, is at Larry and Penny Thompson
Park and adjoining publicly owned
properties at Richmond Field.
Given the species’ narrow range and
the small number of individuals that
exist where it occurs, Blodgett’s
silverbush is vulnerable to natural
disturbance events such as hurricanes
and tropical storms. Other threats
include fire suppression and invasive
exotic pest plants. However, intensive
management and biological control
efforts are aimed at eradicating Old
World climbing fern (Lygodium
microphyllum) and improving the
overall quality of management on
conservation lands. Therefore, based on
continuing nonimminent threats of a
moderate magnitude, we retain a listing
priority number of 11 for Blodgett’s
silverbush.
Artemisia campestris ssp. borealis
var. wormskioldii (Northern
wormwood)—The following summary is
based on information from our files. No
new information was provided in the
petition received on May 11, 2004.
Historically known from eight sites,
northern wormwood is currently known
from only two populations in Klickitat
and Grant Counties, Washington. This
plant is restricted to exposed basalt,
cobbly-sandy terraces, and sand habitat
along the shore and on islands in the
Columbia River. The two sites are
separated by 200 miles (322 kilometers)
of the Columbia River and three large
hydroelectric dams. The Klickitat
County population is apparently
declining; the Grant County population
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24909
is stable or declining. Surveys of
apparently suitable habitat along 55
miles of the Hanford Reach (the wild
flowing reach of the Columbia River)
have not detected any additional plants.
Threats to Northern wormwood include
habitat loss due to dam, railroad, and
highway construction; recreational use;
manipulation of waterflows by
hydroelectric dams resulting in flooding
and alteration of historic waterflows;
nonnative plants; vulnerability to
ecological and genetic factors and
naturally occurring, random events; and
hybridization with two other species of
Artemisia. The magnitude of threats
continues to be high because the only
two remaining populations are widely
separated and occur in a dynamic
habitat affected by frequently changing
water levels. Threats continue to be
imminent due to small population sizes
and the potential for the elimination of
one or both populations by a single
disturbance. We retain a listing priority
number of 3 for this subspecies.
Astelia waialealae (Painiu)—The
following summary is based on
information contained in our files. No
new information was provided in the
petition received on May 11, 2004.
Painiu is a perennial herb found in
Metrosideros polymorpha dominated
mixed montane bog on Kauai, Hawaii.
Astelia waialealae is known from 3
populations in three bogs within the
Alakai swamp region of Kauai, totaling
35 clumps which may only represent 10
to 15 genetically distinct individuals.
Thirty clumps are found in one bog.
While the species has always been
restricted to the bogs of the Alakai, it
may have occurred in more bogs in the
past and in greater numbers. The largest
individual, less than 12 inches (30
centimeters) in diameter, is not
reproducing, and no regeneration has
been observed from 1995 to the present.
This species is threatened by pigs that
prey upon and trample plants and
seedlings, degrade and/or destroy
habitat, and spread the nonnative plants
Juncus planifolius and Andropogon
virginicus, which compete with Astelia
waialealae. Because the threats continue
to be of a high magnitude and are
considered imminent, we retain a listing
priority number of 2 for this species.
Astragalus equisolensis (Horseshoe
milkvetch)—The following summary is
based on information from our files. No
new information was provided in the
petition received on May 11, 2004. The
Horseshoe milkvetch, Astragalus
equisolensis, is a plant within the
Fabaceae or Leguminosae (Pea family)
only found in Uintah County, Utah.
Horseshoe milkvetch is associated with
the mixed desert and salt desert shrub
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communities that are generally
dominated by sagebrush (Artemisia sp.),
shadscale (Atriplex confertiolia) and
horsebrush (Tetradymia nuttallii).
Horseshoe milkvetch is found on the
Duchesne River Formation at elevations
between 4,800 and 5,200 feet. Based on
surveys in 1992, the population was
estimated at approximately 10,000
individuals. Threats continue to be
habitat degradation and fragmentation
associated with oil and gas exploration;
road development; off-road vehicle use;
and species instability due to low
numbers. Currently the threats are low
to moderate as only a few wells have
been drilled in Horseshoe milkvetch
habitat; however, these threats continue
to be imminent as oil and gas
development is foreseeable in the near
future. Because of these factors, we
retain a listing priority of 8 for this
species.
Astragalus tortipes (Sleeping Ute
milkvetch)—The following summary is
based on information from our files. No
new information was provided in the
petition received on May 11, 2004.
Astragalus tortipes 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, a total of 3,744 plants
were recorded at 24 locations covering
500 acres on a specific substrate within
an overall range of 64,000 acres.
Available information from 2000
indicates that the species remains
stable. Previous and ongoing threats
from borrow pit excavation, off-highway
vehicles, an expanding junkyard,
irrigation canal construction, and a
prairie dog colony have had minor
impacts that reduced the range and
number of plants by small amounts. Oil
and gas development may occur in the
future within the species’ range, but is
not likely within the substrate that
supports occupied habitat. Therefore,
we retain a listing priority number of 8
for A. tortipes.
Bidens amplectens (Kookooalu)—See
above in ‘‘Summary of Listing Priority
Changes in Candidates.’’ The above
summary is based on information
contained in our files. No new
information was provided in the
petition received on May 11, 2004.
Bidens campylotheca ssp. pentamera
(Kookooalu)—See above in ‘‘Summary
of Listing Priority Changes in
Candidates.’’ The above summary is
based on information contained in our
files. No new information was provided
in the petition received on May 11,
2004.
Bidens campylotheca ssp. waihoiensis
(Kookooalu)—The following summary is
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based on information contained in our
files. No new information was provided
in the petition received on May 11,
2004. Kookooalu is an erect, perennial
found in wet Acacia-Metrosideros forest
on Maui, Hawaii. This subspecies is
known from one population of 200
individuals, restricted to the island of
Maui. This subspecies is highly
threatened by ongoing cattle grazing that
degrades and destroys habitat. Because
the threats continue to be of a high
magnitude and are considered
imminent, we retain a listing priority
number of 3 for this subspecies.
Bidens conjuncta (Kookooalu)—The
following summary is based on
information contained in our files. No
new information was provided in the
petition received on May 11, 2004.
Kookooalu is an erect perennial herb
found in Metrosideros-Dicronopteris
lowland to montane wet forest and
shrubland on Maui, Hawaii. Six
populations are known, and the number
of individual plants totals
approximately 2,200 scattered
throughout upper elevation drainages of
west Maui. Although the overall range
of the species has not changed, the
number of remaining individuals has
declined over the last decade or so. This
species is moderately threatened by pigs
and rats that degrade and destroy
habitat, and that eat vegetative parts and
fruit of B. conjuncta, and by nonnative
plants that outcompete and displace it.
Because the threats continue to be of a
moderate magnitude and are considered
imminent, we retain a listing priority
number of 8 for this species.
Bidens micrantha ssp. ctenophylla
(Kookooalu)—See above in ‘‘Summary
of Listing Priority Changes in
Candidates.’’ The above summary is
based on information contained in our
files. No new information was provided
in the petition received on May 11,
2004.
Brickellia mosieri (Florida brickellbush)—See above in ‘‘Summary of
Listing Priority Changes in Candidates.’’
The above summary is based on
information contained in our files. No
new information was provided in the
petition received on May 11, 2004.
Calamagrostis expansa (no common
name)—See above in ‘‘Summary of
Listing Priority Changes in Candidates.’’
The above summary is based on
information contained in our files. No
new information was provided in the
petition received on May 11, 2004.
Calamagrostis hillebrandii (no
common name)—See above in
‘‘Summary of Listing Priority Changes in
Candidates.’’ The above summary is
based on information contained in our
files. No new information was provided
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in the petition received on May 11,
2004.
Calliandra locoensis (no common
name)—The following summary is
based on information from our files. No
new information was provided in the
petition received on May 11, 2004.
Calliandra locoensis is currently known
from only two localities in the
municipalities of Yauco and Sabana
Grande, in southwestern Puerto Rico.
The restricted distribution, urban
development, management practices,
small number of individuals in the two
populations, and catastrophic natural
events are high threats to this species.
These threats are not imminent because
both localities fall within protected
lands, but they continue to be of a high
magnitude since they affect both of this
plant’s known populations. Therefore,
we retain a listing priority of 5 for this
species.
Calochortus persistens (Siskiyou
mariposa lily)—See above in ‘‘Summary
of Listing Priority Changes in
Candidates.’’ The above summary is
based on information contained in our
files and the petition received on
September 10, 2001.
Calyptranthes estremerae (no
common name)—The following
summary is based on information from
our files. No new information was
provided in the petition received on
May 11, 2004. Calyptranthes estremerae
is a small tree from the subtropical
moist forest of northwestern Puerto
Rico, in the municipalities of Camuy,
Utuado, and Arecibo. The small number
of individuals in the two populations,
the species’ limited distribution,
catastrophic natural events, and the
potential destruction of specimens due
to expansion of recreational facilities
threaten the species. These threats,
while continuing to be a high
magnitude, are not imminent, because
the largest known population is found
within protected lands. We retain a
listing priority of 5 for this species.
Canavalia napaliensis (Awikiwiki)—
See above in ‘‘Summary of Listing
Priority Changes in Candidates.’’ The
above summary is based on information
contained in our files. No new
information was provided in the
petition received on May 11, 2004.
Canavalia pubescens (Awikiwiki)—
The following summary is based on
information contained in our files. No
new information was provided in the
petition received on May 11, 2004.
Awikiwiki is a perennial climber found
in lowland dryland forest on Maui,
Lanai, Kauai, and is possibly on the
island of Niihau, Hawaii. This species is
known from 10 populations totaling less
than 200 individuals. This species is
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highly threatened by development; goats
that eat this plant and degrade and
destroy habitat, and by nonnative plants
that outcompete and displace them.
Because the threats continue to be of a
high magnitude and are considered
imminent, we retain a listing priority
number of 2 for this species.
Castilleja aquariensis (Aquarius
paintbrush)—The following summary is
based on information from our files. No
new information was provided in the
petition received on May 11, 2004. The
Aquarius paintbrush is a plant, within
the Scrophulariaceae or Figwort family,
found only on the Aquarius plateau of
south central Utah. Habitat
characteristics are meadow openings
and open spruce-fir stands at 9,800 to
11,300 feet in elevation. Trends for this
species appear to be cyclic with
individual plants ranging from 15,000 to
45,000 depending on the year. A
correlation may exist between
precipitation and plant numbers.
Threats to the Aquarius paintbrush are
wildlife and domestic livestock grazing
that adversely affects this species by
trampling and consumption of plants;
concentration of livestock associated
with water sources; grasshopper, cricket
or aphid infestations; road construction
for access to recreational and timber
harvesting areas; unauthorized off-road
vehicle activity; drought conditions; and
reduction of genetic diversity due to low
population numbers and fragmentation.
Monitoring data suggests that in good
years, Aquarius paintbrush are able to
regenerate and survive under domestic
livestock grazing, but the species
appears to be more affected by grazing
during drought conditions. The overall
impacts to this species continue to be of
a moderate to low magnitude of threat.
Because livestock and wildlife
associated with Aquarius paintbrush are
present, grazing threats continue to be
imminent. Because of these factors, we
retain a listing priority number of 8 for
this species.
Castilleja christii (Christ’s
paintbrush)—The following summary is
based on information contained in our
files and the petition received on
January 2, 2001. Christ’s paintbrush is
endemic to subalpine meadow and
sagebrush habitats in the upper
elevations of the Albion Mountains,
Cassia County, Idaho. The single
population of this species, which covers
only 81 ha (200 ac), is restricted to the
summit of Mount Harrison. The
population appears to be stable,
although the species is threatened by a
variety of activities. Most threats
involve seasonal impacts, including
unauthorized ORV use that results in
erosion of the plant’s habitat and
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mortality of individual plants; livestock
grazing that adversely affects Christ’s
paintbrush by trampling and
consumption of plants, which results in
reduced reproductive success; trampling
by hikers and road maintenance
activities. Also, road maintenance
activities threaten the species through
the introduction of exotic plants. For
example, in 1997 smooth brome
(Bromus inermis) was planted along a
road after a paving project. By 2004, the
smooth brome had expanded from the
roadside several hundred feet into the
Christ’s paintbrush population and may
pose a significant threat to the species.
The Forest Service has constructed
fencing that will largely reduce the
threat of seasonal livestock trespass
impacts for most of the Mt. Harrison
summit area. The Forest Service has and
continues to build rock barriers along
roads within Christ’s paintbrush habitat
to further discourage off-road vehicle
use. Most recently, the Forest Service
designated a large portion of the
population as a Botanical Special
Interest Area and, in conjunction with
our Field Office, installed conservation
signs that provide information about the
species. Due to these efforts, the threats
continue to be nonimminent and are of
a low to moderate magnitude. Therefore,
we retain a listing priority number of 11
for this species.
Chamaecrista lineata var. keyensis
(Big Pine partridge pea)—The following
summary is based on information in our
files. No new information was provided
in the petition received on May 11,
2004. This pea is endemic to the lower
Florida Keys. Historically, it was known
from Big Pine, No Name, Ramrod, and
Cudjoe Keys (Monroe County, Florida).
It is now believed to be restricted to Big
Pine Key. Roughly 90 percent of its
current range is within the National Key
Deer Refuge. The Big Pine partridge pea
is well distributed on Big Pine Key, with
a population estimate of roughly 10,000
individuals. It is restricted to pine
rockland communities and hardwood
hammock edges. Pine rocklands
encompass approximately 582 hectares
(1,438 acres) on Big Pine Key. Pine
rockland communities are maintained
by relatively frequent fires. In the
absence of fire, woody encroachment
ensues and shades out the pea. Lack of
fire poses the greatest threat to the pea.
The Refuge has an active prescribed fire
program, though with many constraints.
Sea level rise constitutes another threat
somewhat less imminent, although of
greater magnitude. Based on
nonimminent threats that continue to be
of high magnitude, we retain a listing
priority number of 6 for the Big Pine
partridge pea.
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Chamaesyce deltoidea pinetorum
(Pineland sandmat)—See above in
‘‘Summary of Listing Priority Changes in
Candidates.’’ The above summary is
based on information contained in our
files. No new information was provided
in the petition received on May 11,
2004.
Chamaesyce deltoidea ssp. serpyllum
(Wedge spurge)—The following
summary is based on information in our
files. No new information was provided
in the petition received on May 11,
2004. Wedge spurge is a small herb, flat
to the ground, forming patches of
rounded or wedge-shaped leaves among
the limestone rocks. It has always been
restricted to Big Pine Key in Monroe
County, Florida. Roughly 90 percent of
the range falls within the National Key
Deer Refuge. It is not widely or evenly
distributed, occurring within 22 percent
of 145 sample plots in pine rockland.
The total population is on the order of
1,001 to 10,000 plants. It is restricted to
pinelands on limestone rock (pine
rockland), at sites with extensive
exposed rock at the surface, low total
understory cover and low hardwood
density. Pine rocklands encompass
approximately 582 hectares (1,438
acres) on Big Pine Key. These
communities are maintained by
relatively frequent fires; without fire,
tropical shrubs and trees encroach and
the spurge is eventually shaded out. Fire
restrictions pose the greatest measurable
threat. The National Key Deer Refuge
has an active prescribed fire program,
though with many constraints. Sea level
rise during the twentieth century was
shown to have affected upland
vegetation in the lower Keys. This
threat, though less imminent, is
ultimately of greater magnitude.
Hurricanes pose additional threats.
Therefore, we assign the wedge spurge
a listing priority number of 6 due to
continuing nonimminent threats of a
high magnitude.
Chamaesyce eleanoriae (Akoko)—See
above in ‘‘Summary of Listing Priority
Changes in Candidates.’’ The above
summary is based on information
contained in our files. No new
information was provided in the
petition received on May 11, 2004.
Chamaesyce remyi var. kauaiensis
(Akoko)—See above in ‘‘Summary of
Listing Priority Changes in Candidates.’’
The above summary is based on
information contained in our files. No
new information was provided in the
petition received on May 11, 2004.
Chamaesyce remyi var. remyi
(Akoko)—See above in ‘‘Summary of
Listing Priority Changes in Candidates.’’
The above summary is based on
information contained in our files. No
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new information was provided in the
petition received on May 11, 2004.
Charpentiera densiflora (Papala)—See
above in ‘‘Summary of Listing Priority
Changes in Candidates.’’ The above
summary is based on information
contained in our files. No new
information was provided in the
petition received on May 11, 2004.
Chorizanthe parryi var. fernandina
(San Fernando Valley spineflower)—
The following summary is based on
information contained in our files and
the petition received on December 14,
1999. San Fernando Valley spineflower
is currently known from only two
populations. The plants are threatened
by habitat loss due to residential
development, competition from
nonnative plants (e.g., several nonnative
grasses), random events such as erosion
and fire, and the potential loss of the
native pollinator community due to
competition with and predation by the
nonnative Argentine ants (Linepithema
humilis).
The site in Los Angeles County, the
Newhall Ranch, is proposed for
residential development that has the
potential to cause the loss of most, if not
all, of the remaining plants at that site.
Representatives of Newhall Ranch
informed us that they intended to
pursue a Candidate Conservation
Agreement (CCA) for the plant, and, in
2004, presented us with a preliminary
plan that would avoid removing
approximately 74 percent of the area the
plant is believed to occupy. However,
the level of detail available was not
sufficient for us to conclude that the
preserved populations would be
appropriately buffered from adjacent
land uses, or that sufficient native
vegetation would remain in proximity to
the preserved areas to support a
pollinator community. We received a
draft CCA in early February 2005 but
have not yet thoroughly reviewed it.
The site in Ventura County, the
former Ahmanson Ranch, is now under
the auspices of the Santa Monica
Mountains Conservancy, a joint powers
authority operated by the State to
conserve lands within the
Conservancy’s sphere of influence. As a
result, the direct threats to the species
from the former Ahmanson Ranch
development plan have been
eliminated, and we are working with the
new landowners to manage the site for
the benefit of Chorizanthe parryi var.
fernandina. Since the threats continue
to be of a high magnitude but are
nonimminent, we retain a listing
priority number of a 6 for this plant
variety.
Chromolaena frustrata (Cape Sable
thoroughwort)—See above in ‘‘Summary
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of Listing Priority Changes in
Candidates.’’ The above summary is
based on information contained in our
files. No new information was provided
in the petition received on May 11,
2004.
Consolea corallicola (Florida
semaphore cactus)—The following
summary is based on information in our
files. No new information was provided
in the petition received on May 11,
2004. This species is endemic to the
Florida Keys and is known to naturally
occur only at Little Torch Key and Swan
Key. It was discovered on Big Pine Key
in 1919 but has since been extirpated
there as a result of road building and
poaching. The Florida semaphore 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. About seven mature plants exist
in the population at The Nature
Conservancy’s Torchwood Hammock
Preserve on Little Torch Key. Two
sexual morphs (males and weak
hermaphrodites) comprise the extant
population on Little Torch Key. The
female sex morph is absent from the
population and sexual reproduction at
this site without human intervention is
not possible. Regeneration in this
population is restricted to clonal
propagation. At least 629 plants were
discovered on Swan Key, Biscayne
National Park in November of 2001. The
reproductive biology of the population
found on Swan Key is yet to be
determined. Outplanting has resulted in
the reestablishment of a population in
Dagny Johnson Key Largo Hammock
Botanical State Park in North Key Largo.
The causes for the population decline of
this species include destruction or
modification of habitat, predation from
nonnative Cactoblastis cactorum moths,
unauthorized collection, and the
occurrence of hurricanes and other
significant natural disturbance events.
Based on imminent threats that
continue to be of a high magnitude, we
retain a listing priority number of 2 for
the Florida semaphore cactus.
Cordia rupicola (no common name)—
The following summary is based on
information from our files. No new
information was provided in the
petition received on May 11, 2004.
Cordia rupicola is a small shrub that is
˜
found in the municipalities of Penuelas
´
and Guanica in southern Puerto Rico, as
well as the island of Anegada in the
British Virgin Islands. The current
status of the Anegada population is not
known. The restricted distribution,
urban expansion, and significant natural
disturbance events are threats to the
Puerto Rico population. Because the
threats to this species continue to be
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imminent and of a high magnitude, due
to only a small fraction of the species’
known population occurring within
protected lands, we retain a listing
priority of 2.
Cyanea asplenifolia (Haha)—The
following summary is based on
information contained in our files. No
new information was provided in the
petition received on May 11, 2004.
Cyanea asplenifolia is a shrub found in
Acacia-Metrosideros forest on Maui,
Hawaii. Cyanea asplenifolia was
thought to be extinct following
collections in 1920 on west Maui until
it was rediscovered in 1995 on east
Maui. Two additional populations of
approximately 30 individuals total have
been rediscovered on west Maui, but the
largest population is found in Kipahulu
Valley on east Maui. Until 1991, when
flowering occurred, the Kipahulu
population was thought to be Cyanea
grimesiana ssp. grimesiana. Flowers
and fruits led to a valid identification of
this population as Cyanea asplenifolia.
In 1991, 350 individuals were counted.
During a return visit in 1995, the
population was estimated to be only
approximately 200 individuals, showing
a decline in the population for reasons
not determined. Currently, this
population has declined to a few
individuals. An additional 25
individuals have been found in
Makawao and Koolau forest reserves on
east Maui. This species is threatened by
pigs and goats that eat this plant and
degrade and destroy its habitat, by rats
and slugs that directly prey upon and
defoliate the species, and by nonnative
plants that outcompete and displace it.
Because the threats continue to be of a
high magnitude and are imminent, we
retain a listing priority number of 2 for
this species.
Cyanea calycina (Haha)—See above in
‘‘Summary of Listing Priority Changes in
Candidates.’’ The above summary is
based on information contained in our
files. No new information was provided
in the petition received on May 11,
2004.
Cyanea eleeleensis (Haha)—The
following summary is based on
information contained in our files. No
new information was provided in the
petition received on May 11, 2004.
Cyanea eleeleensis is a shrub found in
wet forest on Kauai, Hawaii. This
species was discovered in 1977, known
from one population totaling less than
ten individuals in Wainiha Valley on
Kauai. This species is highly threatened
by pigs that degrade and destroy habitat,
by rats and slugs that eat this plant, and
by nonnative plants that outcompete
and displace it. Because the threats
continue to be of a high magnitude and
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are considered imminent, we retain a
listing priority number of 2 for this
species.
Cyanea kuhihewa (Haha)—The
following summary is based on
information contained in our files. No
new information was provided in the
petition received on May 11, 2004.
Cyanea kuhihewa is a shrub found in
Metrosideros polymorpha-Dicranopteris
linearis lowland wet forest on Kauai,
Hawaii. This recently discovered
species is known from one population
totaling 6 individuals in Limahuli
Valley on Kauai. This species was
originally included in the proposed
rulemaking for Kauai II plant species
submitted to the Regional Office but was
removed from the proposed rule
published in 60 FR 49359 on October 2,
1995, because the species had not yet
been described and published at that
time. In 2003, the last known individual
in the wild died, but prior to that time,
seeds were collected for genetic storage,
and the species is still found in
cultivation. This species is highly
threatened by pigs that degrade and
destroy habitat, by rats and slugs that
eat this plant, and by nonnative plants
that outcompete and displace it.
Because the threats continue to be of a
high magnitude and are considered
imminent, we retain a listing priority
number of 2 for this species.
Cyanea kunthiana (Haha)—See above
in ‘‘Summary of Listing Priority Changes
in Candidates.’’ The above summary is
based on information contained in our
files. No new information was provided
in the petition received on May 11,
2004.
Cyanea lanceolata (Haha)—See above
in ‘‘Summary of Listing Priority Changes
in Candidates.’’ The above summary is
based on information contained in our
files. No new information was provided
in the petition received on May 11,
2004.
Cyanea obtusa (Haha)—The following
summary is based on information
contained in our files. No new
information was provided in the
petition received on May 11, 2004.
Cyanea obtusa is a shrub found in
Metrosideros polymorpha mixed mesic
forest on Maui, Hawaii. Cyanea obtusa
was thought to be extinct following the
initial collections from 1841 to 1919 on
east and west Maui until it was
rediscovered in 1981 on east Maui. The
one known population was extirpated
by 1989. In 1996, the species was
rediscovered on east Maui, in a
population of only four individuals. In
1999, additional plants were found,
increasing the known populations to six
and the known number of individuals to
approximately 30. This species is highly
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threatened by goats, pigs, cattle, rats,
and slugs that eat this plant and degrade
and destroy habitat, and by nonnative
plants that outcompete and displace it.
Because the threats continue to be of a
high magnitude and are considered
imminent, we retain a listing priority
number of 2 for this species.
Cyanea tritomantha (Aku)—See above
in ‘‘Summary of Listing Priority Changes
in Candidates.’’ The above summary is
based on information contained in our
files. No new information was provided
in the petition received on May 11,
2004.
Cyrtandra filipes (Haiwale)—The
following summary is based on
information contained in our files. No
new information was provided in the
petition received on May 11, 2004.
Haiwale is a shrub found in lowland
wet and mesic forest on Maui and
Molokai, Hawaii. Historically rare,
Cyrtandra filipes was typically found in
southeastern Molokai and west Maui.
Currently, this species is known from
three populations, one on Molokai and
two on Maui, totaling approximately
2,200 individuals. There is some
question as to the taxonomic 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 population of a
few individuals remaining. This species
is highly threatened by pigs and rats
that degrade and destroy habitat, by
deer that eat this plant, and by
nonnative plants that outcompete and
displace it. Because the threats continue
to be of a high magnitude and are
considered imminent, we retain a listing
priority number of 2 for this species.
Cyrtandra kaulantha (Haiwale)—See
above in ‘‘Summary of Listing Priority
Changes in Candidates.’’ The above
summary is based on information
contained in our files. No new
information was provided in the
petition received on May 11, 2004.
Cyrtandra oenobarba (Haiwale)—See
above in ‘‘Summary of Listing Priority
Changes in Candidates.’’ The above
summary is based on information
contained in our files. No new
information was provided in the
petition received on May 11, 2004.
Cyrtandra oxybapha (Haiwale)—The
following summary is based on
information contained in our files. No
new information was provided in the
petition received on May 11, 2004.
Cyrtandra oxybapha is a shrub found in
Metrosideros polymorphaCheirodendron trigynum montane wet
forest to mesic Acacia-Metrosideros
forest on Maui, Hawaii. Historically
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rare, Cyrtandra oxybapha was typically
found in wet forest on the island of
Maui. Currently, this species is known
only from one population totaling 250 to
300 individuals in the Kahikinui area of
east Maui. This species is highly
threatened by pigs that degrade and
destroy habitat, and by nonnative plants
that outcompete and displace it.
Because the threats continue to be of a
high magnitude and are considered
imminent, we retain a listing priority
number of 2 for this species.
Cyrtandra sessilis (Haiwale)—The
following summary is based on
information contained in our files. No
new information was provided in the
petition received on May 11, 2004.
Cyrtandra sessilis is a shrub found in
wet gulch bottoms and slopes of mesic
valleys and wet forests on Oahu,
Hawaii. This species is known from two
populations totaling approximately 50
individuals in the Waikane area of the
Koolau Mountains. This species is
highly threatened by pigs that degrade
and or destroy habitat and by nonnative
plants that outcompete and displace it.
Because the threats continue to be of a
high magnitude and are considered
imminent, we retain a listing priority
number of 2 for this species.
Dalea carthagenensis floridana
(Florida prairie-clover)—See above in
‘‘Summary of Listing Priority Changes in
Candidates.’’ The above summary is
based on information contained in our
files. No new information was provided
in the petition received on May 11,
2004.
Dichanthelium hirstii (Hirsts’ panic
grass)—The following summary is based
on information from our files. No new
information was provided in the
petition received on May 11, 2004.
Dichanthelium hirstii, a perennial grass,
produces erect leafy flowering stems
from May to October. Dichanthelium
hirstii occurs in coastal plain
intermittent ponds, usually in wet
savanna or pine barren habitats and is
found at only one site in New Jersey,
one site in Delaware, and two sites in
North Carolina. While all four extant
Dichanthelium hirstii populations are
located on public land or privately
owned conservation lands, natural
threats to the species from encroaching
vegetation and fluctuations in climatic
conditions remain of concern and may
be exacerbated by anthropomorphic
factors occurring adjacent to the species’
wetland habitat. Given the low numbers
of plants found at each site, even minor
changes in the species’ habitat could
result in local extirpation. Loss of any
known sites could result in a serious
protraction of the species range.
However, the most immediate and
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severe of the threats to this species (i.e.,
ditching of the Labounsky Pond site,
and encroachment of aggressive
vegetative competitors) have been
curtailed or are being actively managed
by The Nature Conservancy at the New
Jersey site, the Delaware Division of
Fish and Wildlife, and Delaware Natural
Heritage Program at the Assawoman
Pond site, and the Marine Corps at the
Camp Lejeune site in North Carolina.
Based on continued threats of a high
magnitude but low imminence, we
retain a listing priority number of 5 for
this species.
Digitaria pauciflora (Florida pineland
crabgrass)—The following summary is
based on information in our files. No
new information was provided in the
petition received on May 11, 2004. This
perennial grass grows up to 3 feet tall.
It is almost entirely restricted to Long
Pine Key, an island of pineland and
marl prairies surrounded by wetlands in
Everglades National Park, Miami-Dade
County, Florida. It was observed once in
a ‘‘transverse glade’’ at a site now
managed by Miami-Dade County at the
Richmond pine rocklands. Florida
pineland crabgrass occurs most
commonly at the margin between pine
rockland and marl prairie, overlapping
somewhat into both of these ecosystems.
These habitats, particularly marl prairie,
flood for one to several months during
the wet season. Pine rocklands and their
associated prairies are fire-maintained,
with a natural fire frequency of 3 to 7
years for pine rocklands and perhaps
slightly more frequent for marl prairies.
In the absence of fire, tropical
hardwoods quickly encroach. This grass
may once have occurred in pinelands of
what is now the Miami urban area,
based on a specimen collected in 1903.
Essentially no suitable habitat appears
to remain outside of Everglades National
Park. Threats to Florida pineland
crabgrass from invasive exotic plants
have been managed by the National Park
Service, but the threat of Old World
climbing fern and other new exotic
plants within the decade are likely to be
realized. Based on nonimminent threats
that continue to be of a high magnitude,
we retain a listing priority number of 5
for the Florida pineland crabgrass.
Dubautia imbricata ssp. imbricata
(Naenae)—See above in ‘‘Summary of
Listing Priority Changes in Candidates.’’
The above summary is based on
information contained in our files. No
new information was provided in the
petition received on May 11, 2004.
Dubautia plantaginea ssp. magnifolia
(Naenae)—The following summary is
based on information contained in our
files. No new information was provided
in the petition received on May 11,
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2004. Dubautia plantaginea ssp.
magnifolia is a shrub found in bogs and
wet forest on Kauai, Hawaii. This
recently rediscovered species is known
from two populations totaling 100
individuals near the summit of
Waialeale on the island of Kauai. This
species is highly threatened by pigs that
degrade and destroy habitat and by
nonnative plants that outcompete and
displace it. Because the threats continue
to be of a high magnitude and are
ongoing (i.e., imminent), we retain a
listing priority number of 3 for this
subspecies.
Dubautia waialealae (Naenae)—See
above in ‘‘Summary of Listing Priority
Changes in Candidates.’’ The above
summary is based on information
contained in our files. No new
information was provided in the
petition received on May 11, 2004.
Echinomastus erectocentrus var.
acunensis (Acuna cactus)—The
following summary is based on
information contained in our files and
the petition 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 1300–2000
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 (OPCNM), 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 OPCNM 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 OPCNM in the past. While the
threats continue to be of a high
magnitude, they are currently
nonimminent. Thus, we retain a listing
priority number of 6 for this cactus
variety.
Erigeron basalticus (Basalt daisy)—
The following summary is based on
information from our files. No new
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information was provided in the
petition received on May 11, 2004. This
is a small, herbaceous, perennial plant
in the Asteraceae (sunflower) family.
The species is endemic to Yakima and
Kittitas Counties, Washington, and
occurs on canyon walls along the
Yakima River and Selah Creek, a
tributary of the Yakima River. The
species occupies approximately 165 ac
(67 ha) within its known distribution of
approximately 20 mi2 (52 km2). Basalt
daisy only grows in small crevices on
basalt cliffs. The total population of
roughly 7,000 plants is distributed
among 8 potentially interbreeding
subpopulations. The overall size of the
population, both in numbers of plants
and total area occupied, has remained
relatively stable since at least 1988.
However, the numbers of individuals in
the four smallest subpopulations have
decreased substantially, and two
subpopulations currently support fewer
than 20 plants each. The causes of these
declines, or whether they represent a
recent or longterm trend in the
subpopulations, are unknown. The
extremely limited range and specific
habitat requirements of basalt daisy
make it vulnerable to localized impacts,
including threats from adjacent
herbicide and pesticide spraying from
agricultural activities and highway/
railroad maintenance. In addition,
quarrying in the vicinity of several
subpopulations may destroy individual
plants or negatively impact the species’
habitat. While some threats to the
species have been identified, it is likely
not susceptible to other potential
impacts (e.g., conversion, grazing),
primarily due to the inaccessibility of
the near-vertical basalt cliffs it occupies.
Based on the available information, we
consider the magnitude of threat to
basalt daisy to be moderate-to-low, and
the identified threats continue to be
nonimminent. Therefore, we retain a
listing priority of 11 for this species.
Erigeron lemmonii (Lemmon
fleabane)—The following summary is
based on information contained in our
files and the petition received in July
1975. The species is known from one
site on the Fort Huachuca Military
Reservation of southeastern Arizona.
Approximately 70 individual plants are
at this site. The single largest threat to
the species is from significant wildfire
in the canyon where the plant occurs.
An intense wildfire in the narrow
canyon would almost certainly
desiccate plants on the cliff face,
possibly directly killing individuals or
stressing plants, and, thereby leading to
lower reproductive output. Fort
Huachuca is willing to develop a
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conservation agreement for this species.
Measures have been taken to reduce the
threat of wildfire and also the threats
from recreational rappelling, which is
not allowed on the cliff faces occupied
by the plant. Due to these nonimminent
threats of a high magnitude, we retain
a listing priority number of 5 for this
species.
Eriogonum codium (Umtanum Desert
buckwheat)—The following summary is
based on information from our files. No
new information was provided in the
petition received on May 11, 2004. This
is a long-lived woody perennial plant in
the Polygonaceae (buckwheat) family
that forms low mats. Individual plants
may exceed 100 years of age. The only
known population of the species occurs
exclusively on exposed basalt from the
Lolo Flow of the Wanapum Basalt
Formation in Benton County,
Washington. The population has a
discontinuous distribution along a
narrow, 1.0 mi (1.6 km) long mountain
ridge top. It is unknown if the historical
distribution of Umtanum desert
buckwheat was different from the
species’ current distribution. There are
a number of ongoing threats to
Umtanum desert buckwheat. The
species is not well adapted to fire, and
negative impacts to the species from
past fires have been significant. In
addition, Umtanum desert buckwheat
plants are easily damaged by trampling
or crushing by off-road vehicles. Digging
activities and soil disturbance as a result
of prospecting and collecting of
petrified rock may also threaten
Umtanum desert buckwheat as a result
of. Finally, the species appears to have
a very low reproductive rate. The factors
responsible for the lower-than-expected
number of seedlings in the population
are unknown. Possible factors include
low seed production, low seed or pollen
viability, low seedling vigor and
survival, impacts to plant pollinators or
dispersal mechanisms, and insect
predation of seeds. The only known
population of Umtanum desert
buckwheat is small and limited to a
single site. Based on the available
information, we continue to consider
the magnitude of threat to Umtanum
desert buckwheat to be high, and the
identified threats to be imminent. We
retain a listing priority of 2 for
Umtanum desert buckwheat.
Eriogonum kelloggii (Red Mountain
buckwheat)—The following summary is
based on information contained in our
files. No new information was provided
in the petition received on May 11,
2004. Red Mountain buckwheat is a
perennial herb that is endemic to
serpentine habitat of lower montane
forests found between 1,900 and 4,100
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feet. Its distribution is limited to the Red
Mountain and Little Red Mountain areas
of Mendocino County, California, where
it occupies 50 acres and 900 square feet,
respectively. Occupied habitat at Red
Mountain is scattered over 4 square
miles. Total population size is estimated
at between 20,000 and 30,000 plants,
which occur in 44 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 the species is the
potential for mining; the species
distribution overlaps a number of
mining claims, none of which are
currently active. Surface mining, which
would destroy all habitat suitability in
affected areas, would be used to extract
chromium and nickel. The species
distribution by ownership is described
as follows: Federal (Bureau of Land
Management), 69 percent; State of
California, 1 percent; and private, 30
percent. Given the continued high
magnitude but nonimminent threats to
the small, scattered populations, we
retain a listing priority number of 5 for
this species.
Festuca hawaiiensis (no common
name)—See above in ‘‘Summary of
Listing Priority Changes in Candidates.’’
The above summary is based on
information contained in our files. No
new information was provided in the
petition received on May 11, 2004.
Festuca ligulata (Guadalupe fescue)—
The following summary is based on
information from our files and in the
petition received in 1975. Guadalupe
fescue occurs in Big Bend National Park,
Texas, along a trail near Boot Springs.
One of the two Mexican populations
previously known was verified to
persist in 2004. The single known U.S.
population is bisected by a trail and
subject to occasional trampling by
horses and hikers. New trails are
planned that may affect this species, but
plans have not been finalized. The effect
of fire on the species is uncertain. The
magnitude of these threats to Guadalupe
fescue continue to be moderate to low
and nonimminent because Big Bend
National Park is committed to species
management through a conservation
agreement to reduce threats which is yet
to be fully implemented. Based on these
threats imposed on the species, we
retain a listing priority number of 11.
Gardenia remyi (Nanu)—See above in
‘‘Summary of Listing Priority Changes in
Candidates.’’ The above summary is
based on information contained in our
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files. No new information was provided
in the petition received on May 11,
2004.
Geranium hanaense (Nohoanu)—See
above in ‘‘Summary of Listing Priority
Changes in Candidates.’’ The above
summary is based on information
contained in our files. No new
information was provided in the
petition received on May 11, 2004.
Geranium hillebrandii (Nohoanu)—
The following summary is based on
information contained in our files. No
new information was provided in the
petition received on May 11, 2004.
Geranium hillebrandii is a decumbent
subshrub found in bogs on Maui,
Hawaii. Previously known from two
populations totaling approximately 500
individuals, it is currently known from
over 2,000 individuals, the result of
more thorough surveys. This species is
moderately threatened by pigs that
degrade and destroy habitat, and by
nonnative plants that outcompete and
displace it. Because the threats continue
to be of a moderate magnitude and are
considered imminent, we retain a listing
priority number of 8 for this species.
Geranium kauaiense (Nohoanu)—The
following summary is based on
information contained in our files. No
new information was provided in the
petition received on May 11, 2004.
Geranium kauaiense is a decumbent
subshrub found in bogs and bog margins
on Kauai, Hawaii. This species is known
from three populations totaling 100 to
200 individuals in the Alakai Swamp
area. This species is highly threatened
by pigs that eat this plant and degrade
and destroy habitat, and by nonnative
plants that outcompete and displace it.
Because the threats continue to be of a
high magnitude and are considered
imminent, we retain a listing priority
number of 2 for this species.
Gonocalyx concolor (no common
name)—The following summary is
based on information from our files. No
new information was provided in the
petition received on May 11, 2004.
Gonocalyx concolor is a small evergreen
epiphytic shrub found within the dwarf
or elfin forest type in the Carite
Commonwealth Forest in the
municipalities of Guayama, Cayey,
Caguas, San Lorenzo, and Patillas of
southeastern Puerto Rico. The
population previously reported from the
Luquillo Mountains is apparently no
longer extant. The construction of roads
and telecommunication towers, certain
forest management practices, lower
number of specific pollinators,
significant natural disturbance events,
and its limited distribution and
population numbers threaten this
species. Although the magnitude of
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these threats continues to be high, they
are not imminent because the known
populations are found within protected
lands, and initial efforts at propagation
have been successful. Therefore, we
retain a listing priority of 5 for this
species.
Hazardia orcuttii (Orcutt’s
hazardia)—See above in ‘‘Summary of
Listing Priority Changes in Candidates.’’
The above summary is based on
information contained in our files and
the petition received on March 8, 2001.
Hedyotis fluviatilis (Kamapuaa)—See
above in ‘‘Summary of Listing Priority
Changes in Candidates.’’ The above
summary is based on information
contained in our files. No new
information was provided in the
petition received on May 11, 2004.
Helianthus verticillatus (Whorled
sunflower)—The following information
is based on information contained in
our files. No new information was
provided in the petition received on
May 11, 2004. The whorled sunflower is
found in moist, prairie-like openings in
woodlands and along adjacent creeks.
Despite extensive surveys throughout its
range, only six sites are known for this
species. There are two sites documented
for Cherokee County, Alabama; three in
Floyd County, Georgia; and a single site
in Madison County, 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.
The largest population is in Georgia and
is under a conservation easement of 600
acres to The Nature Conservancy. We
continue to assign a listing priority
number of 11 to this species as the
magnitude of threats is considered
‘‘moderate’’ since the largest site is
under permanent protection and the
threats are considered ‘‘nonimminent’’
since the whorled sunflower appears to
withstand some disturbance and there
are no known immediate threats to the
sites.
Hibiscus dasycalyx (Neches River
rose-mallow)—The following summary
is based on information from our files.
No new information was provided in
the petition received on May 11, 2004.
The Neches River rose-mallow is a
perennial woody herb growing 3–7 feet
tall with one or more stems per clump
and white flowers 3–6 inches wide,
consisting of five 2–4-inch-long white
petals with deep red or purple at the
base. The Neches River rose-mallow
appears to be restricted to wetlands, or
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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
species appears to have community
dominance within that narrow band
between high and low water levels in
wetlands exposed to open sun.
However, historical 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 potentially
affect the species’ habitat include
wetland alteration, herbicide use,
grazing, and mowing during the species’
growing and flowering period.
A 1995 status survey of 10 counties
resulted in confirmation or discovery of
the species in only three sites, but in
three separate counties and three
different watersheds, suggesting a
relatively wide historical range. These
three populations are within highway
rights-of-way (ROW) (Ponta site in
Cherokee County; Lovelady in Houston
County; and Highway 94 in Trinity
County) and are monitored by the Texas
Parks and Wildlife Department and are
somewhat protected by a management
agreement with the Texas Department of
Transportation. Because these sites are
still vulnerable to adjacent agricultural
activities such as herbicide spraying,
they support relatively low population
numbers: Ponta (Highway 204) has
ranged from 1 to 5 plants; Lovelady
(Highway 230), 3–14 plants; and
Highway 94, 15–49 plants. Continued
surveys for H. dasycalyx have resulted
in identifying several new populations.
About 300 plants were found on land
owned by the Temple-Inland
Corporation in east Trinity County. A
Candidate Conservation Agreement now
covers this site, but smaller numbers
have been seen in recent years, possibly
due to changes in the wetland’s
hydrology. Another site was discovered
on land owned by the Champion
International Corporation (near White
Rock Creek in west Trinity County). A
Candidate Conservation Agreement was
also established for this site, which
generally supported 300–400 plants.
However, the status of this population is
currently unknown due to a recent
change in ownership.
In west Houston County, a population
of 300–400 plants discovered on private
land has been purchased by the Natural
Area Preservation Association, a land
trust organization, in order to protect
this land in perpetuity. In east Houston
County, a population was recently
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discovered in Compartment 55 in Davy
Crockett National Forest (DCNF) at the
south end of Forest Road 503. This
population is large, but has not yet been
fully tallied. DCNF represents the only
public land within the range of the rosemallow. In 2000, nearly 800 plants were
introduced into Compartments 16 and
20 of the forest as part of a
reintroduction effort. One population
has retained high numbers, but the
second has been impacted by a change
in hydrology. A small dam may be
installed to restore original wetland
conditions. Three more sites in DCNF
have been identified as potential sites
for reintroduction efforts.
Some populations of this species are
at risk of genetic swamping by other
Hibiscus species. Hybridization has
occurred at both the Ponta and Highway
94 sites. Stephen F. Austin State
University (SFASU) is carrying out a
genetic analysis of H. dasycalyx and
similar species to better define
morphological characteristics. SFASU is
also carrying out a habitat study of H.
dasycalyx and developing plants for
reintroduction purposes. Because the
threats continue to be of a high
magnitude and are nonimminent, we
retain a listing priority number of 5 for
the Neches River rose-mallow.
Indigofera mucronata keyensis
(Florida indigo)—See above in
‘‘Summary of Listing Priority Changes in
Candidates.’’ The above summary is
based on information contained in our
files. No new information was provided
in the petition received on May 11,
2004.
Ivesia webberi (Webber ivesia)—The
following summary is based on
information contained in our files. No
new information was provided in the
petition 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
Desert. Currently, the global population
is estimated at approximately 4.8
million individuals at 15 known sites.
The Nevada sites support nearly 98
percent of the total number of
individuals (4.7 million) on about 30
acres of occupied habitat. The California
sites are larger in area, totaling about
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156 acres, but support fewer individuals
(approximately 115,000).
The primary threats to Webber ivesia
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
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, and the State of
Nevada has recently listed the species as
critically endangered, which provides a
mechanism to track future impacts on
private lands. In addition, both the
Forest Service and State of Nevada have
agreed to coordinate closely on all
activities that may affect this species.
For these reasons, we have determined
that the threats to Webber ivesia
continue to be of a high magnitude and
nonimminent and are maintaining the
listing priority number of 5.
Joinvillea ascendens ssp. ascendens
(Ohe)—The following summary is based
on information contained in our files.
No new information was provided in
the petition received on May 11, 2004.
Ohe is an erect herb found in wet
Metrosideros polymorpha forest on the
islands of Kauai, Oahu, Molokai, Maui,
and Hawaii, Hawaii. Joinvillea
ascendens ssp. ascendens is known
from 50 to 100 populations totaling 100
to 200 individuals throughout its range.
Plants are typically found as only one or
two individuals, with miles between
populations. This subspecies is the only
representative of this monotypic species
in Hawaii. This subspecies is highly
threatened by pigs that degrade and
destroy habitat, by an unknown fungus,
and by nonnative plants that
outcompete and displace it. Because the
threats continue to be of a high
magnitude and are considered
imminent, we retain a listing priority
number of 3 for this subspecies.
Keysseria erici (no common name)—
See above in ‘‘Summary of Listing
Priority Changes in Candidates and
Other Taxonomic Changes in
Candidates.’’ The above summary is
based on information contained in our
files. No new information was provided
in the petition received on May 11,
2004.
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Keysseria helenae (no common
name)—See above in ‘‘Summary of
Listing Priority Changes in Candidates
and Other Taxonomic Changes in
Candidates.’’ The above summary is
based on information contained in our
files. No new information was provided
in the petition received on May 11,
2004.
Korthalsella degeneri (Hulumoa)—See
above in ‘‘Summary of Listing Priority
Changes in Candidates.’’ The above
summary is based on information
contained in our files. No new
information was provided in the
petition received on May 11, 2004.
Labordia helleri (Kamakahala)—See
above in ‘‘Summary of Listing Priority
Changes in Candidates.’’ The above
summary is based on information
contained in our files. No new
information was provided in the
petition received on May 11, 2004.
Labordia pumila (Kamakahala)—See
above in ‘‘Summary of Listing Priority
Changes in Candidates.’’ The above
summary is based on information
contained in our files. No new
information was provided in the
petition received on May 11, 2004.
Leavenworthia crassa (Gladecress)—
The following information is based on
information contained in our files. No
new information was provided in the
petition 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 continues to be high for this
species particularly with the limited
number of populations, and the
immediacy of threat is nonimminent
since there are no known projects
planned that would destroy any sites
and the species is able to withstand
some disturbance. Thus, we retain a
listing priority number of 5 for this
species.
Leavenworthia texana (Texas golden
gladecress)—The following summary is
based on information from our files. No
new information was provided in the
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petition received on May 11, 2004. The
Texas golden gladecress is a small
annual member of the mustard family,
with deep, yellow petals only 7–10 mm
long; flowering is February through
March. The gladecress occurs only on
the Weches outcrops of east Texas in
San Augustine County and, historically,
Sabine County. 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 fossilrich complex has produced a rugged
topography of steep, flat-topped hills
and escarpments along Highway 21
through north San Augustine County
and west Sabine County. It has also
created 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.
More than 100 species representing at
least 39 plant families, including the
federally endangered white bladderpod
(Lesquerella pallida), have been
documented on Weches glades. The
gladecress was historically recorded at
eight sites, all in a narrow line along
north San Augustine County and west
Sabine County, following the Weches
formation. All sites are on private land.
Habitat of the species at two of these
locations has since been eliminated due
to glauconite mining. Two more sites
are currently closed to visitors and the
status of the gladecress at these sites is
unknown. However, a large, currently
closed glauconite mine was created just
adjacent to these sites 6 years ago, and
may have altered the area’s hydrology.
One historic site in Sabine County (east
of San Augustine County) was
rediscovered in 1998 and found to
support over 300 plants. However, this
site has since been modified by the
landowner and may no longer support
gladecresses. Only two known
populations remain in San Augustine
County. The Chapel Hill site is less than
0.1 ha (less than 1⁄4 ac) in size and
supports population numbers of 67–200.
The Kardell site is less than 9 m2 (less
than 100 ft2 ) in size and supports 96–
490 plants. An introduced population in
Nacogdoches County has numbered
about 270–300 within an area of about
18 m2 (200 ft2 ). A ninth site may have
been discovered in 1995 but has not
been confirmed in recent years.
Historic gladecress 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 current
threat to existing gladecress populations
is the invasion of nonnative and weedy
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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. Special funding allowed
brushclearing to be carried out in 1995
at several white bladderpod sites (where
gladecress is also located). The project
resulted in large increases in
bladderpod numbers, and also resulted
in the reappearance of gladecress after a
10-year absence at one historic site, and
a possible discovery at a second site.
However, nonnative shrubs have again
invaded these areas. 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 the gladecress vulnerable to
extreme natural disturbance events. A
severe drought in 1999 and 2000 had a
pronounced adverse effect on gladecress
reproduction. Prelisting efforts for the
gladecress include: The collection of
seeds and placement in three State
horticultural labs for possible
reintroduction efforts, a Cooperative
Agreement (now complete) with The
Nature Conservancy of Texas, and
development of a ‘‘Conservation Area
Plan for the San Augustine Glades,’’
which identifies the size and
configuration of conservation units that
will restore and maintain long-term
viability of Weches communities. The
next step is to secure adequate funding
to initiate protection measures.
Landowners of the Chapel Hill and
Kardell sites are aware of the gladecress
and are maintaining current land-use
conditions. Efforts to find additional
sites, and management of known sites,
should be the focus for this species. Due
to the continuing overall high
magnitude and immediacy of the
threats, we retain a listing priority
number of 2 for the Texas golden
gladecress.
Lesquerella globosa (Desvaux) Watson
(Short’s bladderpod)—The following
summary is based on information
contained in our files. No new
information was provided in the
petition received on May 11, 2004.
Short’s bladderpod occurs in Indiana,
Kentucky, and Tennessee. The species
is closely associated with outcrops of
calcareous rock and is found on steep,
rocky, wooded slopes and talus areas,
and along cliff tops and bases and cliff
ledges. Historically, there were at least
57 sites supporting Short’s bladderpod.
Of these 57 sites, only 33 are currently
extant. All remaining populations are
small and vulnerable to extirpation.
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Populations vary in size from 2 to about
1,500 individuals; most contain fewer
than 50 plants. Road construction and
road maintenance have played a
significant role in the decline of the
species. These activities continue to
pose threats to the continued existence
of most populations. Impoundments
and artificial water level manipulation
threatened and, in some cases, have
destroyed sites supporting the species.
Many of the Short’s bladderpod
locations are adjacent to rivers and
streams, and impoundment and water
level manipulation still threaten the
species. Invasive nonnative vegetation is
a significant threat at most sites. Most of
the sites (91 percent) for this species are
under private ownership or within the
rights-of-way of State and county roads.
Of the other sites, two of the Tennessee
sites are on lands managed by the U.S.
Army Corps of Engineers, Nashville
District. One Tennessee site is on Stateowned lands. The Indiana site is on
land owned and managed by The Nature
Conservancy. The threats faced by these
species continue to be significant (i.e.,
high in magnitude); however, it is not
anticipated that they will be subject to
these threats in the immediate future
(next 1–2 years). Therefore, we retain a
listing priority of 5 for this species.
Lesquerella tuplashensis (White
Bluffs bladder-pod)—The following
summary is based on information from
our files. No new information was
provided in the petition received on
May 11, 2004. This is a low-growing,
herbaceous, short-lived, perennial plant
in the Brassicaceae (mustard) family.
Specimens of White Bluffs bladder-pod
were first collected in 1883, although
they were not taxonomically identified
at the time. The same population was
rediscovered in 1994 and formally
described as a distinct species in 1996.
Historically and currently, White Bluffs
bladder-pod has only been known from
this single population that occurs along
the White Bluffs of the Columbia River
in Franklin County, Washington. The
species has a discontinuous distribution
along a narrow band, approximately 33
feet (10 meters) wide by 10.6 miles (17
kilometers) long, at the upper edge of
the bluffs. The species occurs on
cemented, highly alkaline, calcium
carbonate, paleosol (a ‘‘caliche’’ soil).
Eighty-five percent of the population is
on Federal land within the Hanford
Reach National Monument/Saddle
Mountain National Wildlife Refuge,
which is jointly managed by the Service
and U.S. Department of Energy. The
balance of the species’ distribution is on
adjacent private land. White Bluffs
bladder-pod is vulnerable to localized
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impacts because of its extremely limited
distribution and specific habitat
requirements. Water seepage from
adjacent, up-slope agricultural irrigation
causes mass failures and landslides
throughout the length of the White
Bluffs. Approximately 35 percent of the
species’ known range has been
moderately to severely impacted by
landslides. All mass-failures occurring
along the White Bluffs, with one
exception, are found in association with
water seepage. Water, particularly water
from irrigated agriculture adjacent to the
bluffs, is the primary factor triggering
the mass-failures. The entire population
of Lesquerella tuplashensis is downslope of irrigated agricultural land, and
is at risk of landslides induced by waterseepage. The threat is greater in the
southern portion of the species
distribution where irrigated agriculture
is closest, and in several locations
directly adjacent to, the bluffs. Other
threats to White Bluffs bladder-pod
include direct damage of plants by offroad vehicles and recreational activities
(e.g., hiking, bicycling, wildflower
collecting). Based on the available
information, the magnitude of threats to
White Bluffs bladder-pod continue to be
high while these identified threats are
nonimminent. Thus, we retain a listing
priority of 5 for this species.
Linum arenicola (Sand flax)—The
following summary is based on
information in our files. No new
information was provided in the
petition received on May 11, 2004. This
wiry, yellow-flowered perennial herb
with linear leaves is found in tropical
pinelands on limestone rock (pine
rockland), marl prairie, and disturbed
areas on limestone. These habitats are
maintained by periodic fires that control
shrubs and remove leaf litter. Sand flax
is currently known from four sites in
Miami-Dade County, Florida: Camp
Owaissa Bauer (owned by Miami-Dade
County), a private preserve, the Luis
Martinez U.S. Army Reserve Station
Richmond Pine Rocklands (managed by
Miami-Dade County), and Homestead
Bayfront Park (on a limestone canal
levee). In Monroe County (the Florida
Keys), it is present on Big Pine Key
(National Key Deer Refuge; the
Terrestris Preserve, operated by The
Nature Conservancy; and on private
land). It is also present in the Sugarloaf
Hammocks of Florida Keys Wildlife and
Environmental Area on Sugarloaf Key,
operated by the Florida Fish and
Wildlife Conservation Commission. The
total population is about 10,000 plants,
with 1,000 to 3,000 occurring in
completely artificial environments. The
only population exceeding 1,000 plants
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is believed to be the one on Big Pine
Key. The small sizes of the existing
populations and ongoing threats from
exotic pest plants continue to create a
serious risk of extinction for this
species. Therefore, we retain a listing
priority number of 2 for the sand flax.
Linum carteri var. carteri (Carter’s
small-flowered flax)—The following
summary is based on information in our
files. No new information was provided
in the petition received on May 11,
2004. Carter’s small-flowered flax is
found only on the Miami Rock Ridge in
Miami-Dade County, Florida. It is an
erect, annual, or short-lived perennial
herb, often with several stems roughly 1
foot tall. Fewer than 1,000 individuals
were estimated to exist as of 1999.
About that time, a population
disappeared from the Deering Estate at
Cutler, a county-managed conservation
tract. Carter’s small-flowered flax is
currently known from three occurrences
on conservation lands and perhaps six
other locations. It is protected at three
conservation areas owned by MiamiDade County: Camp Owaissa Bauer, R.
Hardy Matheson Preserve, and Rockdale
Pineland. It is present at the U.S.
Department of Agriculture’s Subtropical
Horticulture Research Station (Chapman
Field). It was reported from Homestead
Air Reserve Base, but we do not have
recent confirmation that it is still
present there. It is also present at three
privately owned locations. Residential
and commercial development and
agriculture have substantially reduced
the habitat for this plant, which now
exists in such small numbers that it is
highly vulnerable. Based on imminent
threats that continue to be of a high
magnitude, we retain a listing priority
number of 3 for Carter’s small-flowered
flax.
Lysimachia daphnoides (Lehua
makanoe)—See above in ‘‘Summary of
Listing Priority Changes in Candidates.’’
The above summary is based on
information contained in our files. No
new information was provided in the
petition received on May 11, 2004.
Melicope christophersenii (Alani)—
See above in ‘‘Summary of Listing
Priority Changes in Candidates.’’ The
above summary is based on information
contained in our files. No new
information was provided in the
petition received on May 11, 2004.
Melicope degeneri (Alani)—The
following summary is based on
information contained in our files. No
new information was provided in the
petition received on May 11, 2004.
Melicope degeneri is a small, long-lived
perennial shrub found in mesic to wet
forest on Kauai, Hawaii. Melicope
degeneri was thought to be extinct,
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having only been collected from the
type location along Kokee Stream on the
island of Kauai. Ten individuals of this
species were rediscovered in Hanakoa
Valley in 1993, at a site 4 mi (6 km) from
the type location, one individual in
Koaie Canyon, and one individual at
Pohakuao. Since then, three additional
plants were found in Hanakoa Valley,
bringing the total number of individuals
to 15. This species is threatened by feral
goats, nonnative plants, the black twig
borer, reduced reproductive vigor, and
extinction due to naturally occurring
random events. Because the threats
continue to be of a high magnitude and
are imminent, we retain a listing
priority number of 2 for this species.
Melicope hiiakae (Alani)—The
following summary is based on
information contained in our files. No
new information was provided in the
petition received on May 11, 2004.
Melicope hiiakae is a small tree found
in mesic to wet forest and shrubland on
Oahu, Hawaii. Currently, M. hiiakae is
known from four or five populations of
about 20 individuals in the Koolau
Mountains. This species is threatened
by feral pigs that eat this plant and
degrade and or destroy its habitat,
nonnative plants that outcompete it, and
the black twig borer that potentially
preys upon it. Because the threats
continue to be of a high magnitude and
are imminent, we retain a listing
priority number of 2 for this species.
Melicope makahae (Alani)—The
following summary is based on
information contained in our files. No
new information was provided in the
petition received on May 11, 2004.
Melicope makahae is a shrub or shrubby
tree found in mesic forest on Oahu,
Hawaii. Melicope makahae was
historically found throughout the
central Waianae Mountains. Currently
M. makahae is known from three
populations on three discrete ridges,
totaling approximately 200 individuals.
This species is threatened by goats that
eat this plant and degrade and/or
destroy habitat, nonnative plants that
outcompete it, and the black twig borer
that potentially preys upon it. Because
the threats continue to be of a high
magnitude and are imminent, we retain
a listing priority number of 2.
Melicope paniculata (Alani)—The
following summary is based on
information contained in our files. No
new information was provided in the
petition received on May 11, 2004.
Melicope paniculata is a small tree
found in wet forest dominated by
Metrosideros polymorpha on Kauai,
Hawaii. Historically known from four
scattered populations within central
Kauai, M. paniculata is currently known
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from four populations totaling 110
individuals. This species is threatened
by feral pigs that eat this plant and
degrade and/or destroy habitat,
nonnative plants that outcompete it, and
the black twig borer that potentially
preys upon it. Because the threats
continue to be of a high magnitude and
are imminent, we retain a listing
priority number of 2 for this species.
Melicope puberula (Alani)—See above
in ‘‘Summary of Listing Priority Changes
in Candidates.’’ The above summary is
based on information contained in our
files. No new information was provided
in the petition received on May 11,
2004.
Myrsine fosbergii (Kolea)—See above
in ‘‘Summary of Listing Priority Changes
in Candidates.’’ The above summary is
based on information contained in our
files. No new information was provided
in the petition received on May 11,
2004.
Myrsine mezii (Kolea)—The following
summary is based on information
contained in our files. No new
information was provided in the
petition received on May 11, 2004.
Myrsine mezii is a small many-branched
tree found in mesic forest on Kauai,
Hawaii. This recently rediscovered
species is known from two populations
of only five individuals in Koaie
Canyon. This species is threatened by
feral pigs that eat this plant and degrade
and/or destroy habitat, reduced
reproductive vigor, and by extinction
due to naturally occurring events (e.g.
hurricanes and landslides). Because the
threats continue to be of a high
magnitude and are imminent, we retain
a listing priority number of 2 for this
species.
Myrsine vaccinioides (Kolea)—See
above in ‘‘Summary of Listing Priority
Changes in Candidates.’’ The above
summary is based on information
contained in our files. No new
information was provided in the
petition received on May 11, 2004.
Narthecium americanum (Bog
asphodel)—The following summary is
based on information from our files. No
new information was provided in the
petition 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 historic range of bog
asphodel included New York, New
Jersey, Delaware, North Carolina, and
South Carolina, but is now only found
within the Pine Barrens region of New
Jersey.
As an obligate wetland species, N.
americanum is threatened by changes in
hydrology, loss of habitat due to filling
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or draining of wetlands, flooding as a
result of reservoir construction, and
conversion of natural wetlands to
commercial cranberry bogs. This species
occurs in the Pine Barrens region, and
the Pinelands Commission issues the
State-assumed Clean Water Act Section
404 permits. The Pinelands Commission
grants wetland exemptions to cranberry
production and other agricultural uses.
Illegal wetland filling is occurring. For
example, a cranberry expansion was
illegally completed without a State
permit. In addition, activities not
needing State or federal permits are
occurring in uplands that are indirectly
affecting the wetlands. Natural
succession of vegetation in wetlands
supporting bog asphodel from emergent
(herbaceous) to forested wetlands may
also be contributing to the species’
decline. Suppression of natural
wildfires that would retard succession
or create open wetland savannahs may
be a factor in the decline of the species.
Other factors adversely affecting N.
americanum include trampling, erosion,
and siltation caused by recreationists on
foot or using off-road vehicles.
Approximately 70 percent of known
extant populations occur on Stateowned lands. We are working with the
New Jersey Department of
Environmental Protection to abate
known moderate threats at these sites
from recreational use and erosion.
Approximately 30 percent of the known
extant sites are on privately owned
lands, many of which are threatened by
habitat degradation from on-site or
adjacent residential or commercial
development. Overall, based on these
imminent, moderate threats, we retain a
listing priority number of 8 for this
species.
Nothocestrum latifolium (Aiea)—See
above in ‘‘Summary of Listing Priority
Changes in Candidates.’’ The above
summary is based on information
contained in our files. No new
information was provided in the
petition received on May 11, 2004.
Ochrosia haleakalae (Holei)—The
following summary is based on
information contained in our files. No
new information was provided in the
petition received on May 11, 2004.
Holei is a tree found often on lava in
dry-to-mesic forest on the islands of
Hawaii and Maui, Hawaii. This species
is currently known from three
populations totaling 150 to 250
individuals on east Maui and the island
of Hawaii. This species is threatened by
feral pigs, goats, and cattle that eat this
plant and degrade and/or destroy
habitat, nonnative plants that
outcompete it, and fire. Because the
threats continue to be of a high
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magnitude and are imminent, we retain
a listing priority number of 2 for this
species.
Paronychia congesta (Bushy whitlowwort)—The following summary is based
on information from our files. No new
information was provided in the
petition received on May 11, 2004.
Bushy whitlow-wort is endemic to Jim
Hogg County, Texas. The species is
known from only two population sites,
which occur within 2 miles of each
other, and within the drainage of two
tributaries of the Arroyo Grande. The
bushy whitlow-wort was historically
known only from the type locality
where 2,000 individual plants were
documented. In 1987, a second small
population of 100 individuals was
found 2 miles north-northeast of the
type locality. The limited available data
suggest that the current range and
distribution of the species has not
changed from the historical information
described above. The two known
populations occur on small areas that
cover approximately 5 and 15 acres;
whether populations have expanded or
contracted is unknown.
Threats include destruction,
modification, and fragmentation of
habitat, as well as eradication of
individual plants. Destruction of habitat
due to the conversion of rangeland to
residential development is considered
not imminent, nor of high magnitude
since this part of southern Texas is not
undergoing rapid residential or
industrial development. The alteration
of whitlow-wort habitat by brush
clearing and replanting to nonnative
forage grasses may be declining, as this
type of land conversion has fallen out of
favor across many parts of the Rio
Grande Plains as wildlife-related
income has gained importance in the
regional economy. Currently, the bushy
whitlow-wort is primarily threatened by
the displacement or destruction of
individual plants by construction
activities associated with highways,
pipeline installation, oil and gas
exploration, and well-pad construction.
Right-of-way maintenance activities
may also have negative effects on the
species, and both bushy whitlow-wort
populations are dissected by rights-ofway. At this time, we do not know the
status of oil and gas exploration and
production activities in this area, nor do
we have information on right-of-way
maintenance. With regard to highway
construction and maintenance, the
closest highway is a Farm/Ranch road
that has not been expanded or rebuilt
recently.
The lack of imminent threats to this
plant from habitat conversion is born
out by observations that land use has
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not changed in this area in the past 10
years. No imminent threats have been
identified for this species. All habitats
are located on private land, which
continues to be used for ranching. We
do not have any information to indicate
that a high level of disturbance has
occurred as a result of these activities;
however, access to the property has
been discouraged. Thus, based on
nonimminent threats that continue to be
of a moderate-to-low magnitude, we
retain a listing priority number for this
species is 11.
Pediocactus peeblesianus var.
fickeiseniae (Fickeisen plains cactus)—
The following summary is based on
information from our files. No new
information was provided in the
petition 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 and
Mohave Counties, Arizona. The cactus
grows on exposed layers of Kaibab
limestone on canyon margins and welldrained hills in Navajoan desert or
grasslands. In 1998, the Arizona Game
and Fish Department noted 23 element
occurrences for the species, including
historical ones. Specific population
sizes are unavailable, because
demographic monitoring does not
include individual plant counts and the
species tends to shrink into the ground
during times of drought, making
accurate counts difficult. The major
potential human-induced threats to this
cactus are damage by off-road vehicles
and trampling associated with livestock
grazing. While this cactus is protected
from collection by the Arizona Native
Plant Law, illegal collection is also a
threat for species in the genus
Pediocactus. Because of the continuing
high magnitude of nonimminent threats,
we retain a listing priority number of 6.
Penstemon debilis (Parachute
beardtongue)—See above in ‘‘Summary
of Listing Priority Changes in
Candidates.’’ The above summary is
based on information contained in our
files. No new information was provided
in the petition received on May 11,
2004.
Penstemon grahamii (Graham
beardtongue)—The following summary
is based on information contained in
our files and the petition received on
October 8, 2002. Penstemon grahamii 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. The species population is
estimated at about 7,000 individuals
with 36 known occurrences. Most of the
occupied habitat of P. grahamii is
within developed and expanding oil
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and gas fields with several wells and
access roads within the species’
occupied habitat. The location of P.
grahamii habitat exposes it to possibility
of habitat destruction from off-road
vehicle use, as well as road, pipeline,
and well-site construction in connection
with oil and gas development.
Collection of plants and seeds is a
significant threat due to the actions of
rock-garden enthusiasts to obtain this
very attractive plant. The species is
heavily grazed by wildlife (rodents,
rabbits, and possibly deer) and by
livestock (primarily sheep). Livestock
trampling is affecting some populations.
The threats associated with oil and gas
development within the habitat of P.
grahamii are imminent in light of the
increased seismic survey and petroleum
leasing. Therefore, we retain a listing
priority number of 2 for this species
because the threats continue to be of
high magnitude, and are imminent.
Penstemon scariosus var. albifluvis
(White River beardtongue)—The
following summary is based on
information contained in our files and
the petition 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 three known
populations. Most of the occupied
habitat of the White River beardtongue
is within developed and expanding oil
and gas fields. The location of the
species’ habitat exposes it to destruction
from ORV use, and road, pipeline, and
well-site construction in connection
with oil and gas development. With
such a small population and limited
occupied habitat, any substantial
destruction, modification, or
curtailment of the habitat could have a
highly negative impact on the species.
Additionally, the species is heavily
grazed by wildlife and livestock and is
vulnerable to livestock trampling. Based
on current information, we are retaining
the listing priority number of 6.
Peperomia subpetiolata (Ala ala wai
nui)—The following summary is based
on information contained in our files.
No new information was provided in
the petition received on May 11, 2004.
Ala ala wai nui is a short-lived
perennial herb found in mesic forest on
Maui, Hawaii. This species is known
from a few scattered and declining
populations on windward east Maui,
totaling 100 individuals. Further study
of the population indicates that the 100
individuals may actually represent
clones of only 6 genetically distinct
individuals. This species is threatened
by feral pigs that eat this plant and
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degrade and/or destroy habitat, and by
nonnative plants. Because the threats
continue to be of a high magnitude and
are imminent, we retain a listing
priority number of 2 for this species.
Phacelia submutica (DeBeque
phacelia)—See above in ‘‘Summary of
Listing Priority Changes in Candidates.’’
The above summary is based on
information contained in our files. No
new information was provided in the
petition received on May 11, 2004.
Phyllostegia bracteata (no common
name)—The following summary is
based on information contained in our
files. No new information was provided
in the petition received on May 11,
2004. Phyllostegia bracteata is a
scandent (climbing) perennial herb.
Apparently rare and endemic to the
island of Maui, P. bracteata is known
from three populations totaling no more
than 100 individuals in wet forest
habitat of east Maui. This species is
threatened by feral pigs that eat this
plant and degrade and/or destroy
habitat, nonnative plants that compete
for light and nutrients, and reduced
reproductive vigor and extinction from
naturally occurring events due to small
population sizes. Because the threats
continue to be of a high magnitude and
are imminent, we retain a listing
priority number of 2 for this species.
Phyllostegia floribunda (no common
name)—See above in ‘‘Summary of
Listing Priority Changes in Candidates.’’
The above summary is based on
information contained in our files. No
new information was provided in the
petition received on May 11, 2004.
Phyllostegia hispida (no common
name)—The following summary is
based on information contained in our
files. No new information was provided
in the petition received on May 11,
2004. Phyllostegia hispida is a loosely
spreading many-branched vine found in
wet forest on Molokai, Hawaii. The
historic range of this species was eastern
Molokai. Currently, P. hispida is known
from only two plants, one in The Nature
Conservancy’s Kamakou Preserve and
one in Puu Alii Natural Area Reserve.
This species is threatened by feral pigs
that eat this plant and degrade and/or
destroy habitat, erosion, reduced
reproductive vigor, and extinction due
to naturally occurring events. Because
the threats continue to be of a high
magnitude and are imminent, we retain
a listing priority number of 2 for this
species.
Pittosporum napaliense (Hoawa)—See
above in ‘‘Summary of Listing Priority
Changes in Candidates.’’ The above
summary is based on information
contained in our files. No new
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information was provided in the
petition received on May 11, 2004.
Platanthera integrilabia (Correll) Leur
(White fringeless orchid)—The
following summary is based on
information contained in our files. No
new information was provided in the
petition received on May 11, 2004.
White fringeless orchid occurs in
Alabama, Georgia, Kentucky, South
Carolina, and Tennessee. Historically, it
also occurred in Georgia, Mississippi,
North Carolina, and Virginia. It grows in
wet, boggy areas at the head of streams
and on seepage slopes. It is often
associated with Sphagnum in partially,
but not fully, shaded areas. Historically,
there were at least 90 populations of
white fringeless orchid. Currently there
are only 53 extant sites supporting the
species. Threats to the species include
habitat modification activities such as
road construction, all-terrain vehicles,
residential and commercial
construction, and soil and site
hydrology altering projects that reduce
site suitability for the species. Timber
management is not necessarily
incompatible with the protection and
management of white fringeless orchid.
However, care must be taken during
timber management to ensure that the
hydrology of the bogs that support the
species is not altered, that any heavy
equipment used is kept out of the
species’ habitat, and that the vegetation
is managed in a manner that maintains
suitable light and moisture conditions.
Collecting for commercial and other
purposes, herbivory, and disease all
threatened this species. Invasive
nonnative plants threaten several sites.
The threats faced by this species are
significant; however, it is not
anticipated that it be subject to these
threats in the immediate future (next 1–
2 years). Therefore we retain a listing
priority of 5 for this species.
Platydesma cornuta var. cornuta (no
common name)—See above in
‘‘Summary of Listing Priority Changes in
Candidates.’’ The above summary is
based on information contained in our
files. No new information was provided
in the petition received on May 11,
2004.
Platydesma cornuta var. decurrens
(no common name)—See above in
‘‘Summary of Listing Priority Changes in
Candidates.’’ The above summary is
based on information contained in our
files. No new information was provided
in the petition received on May 11,
2004.
Platydesma remyi (no common
name)—The following summary is
based on information contained in our
files. No new information was provided
in the petition received on May 11,
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2004. Platydesma remyi is a shrub or
shrubby tree found scattered in wet, low
statured forest on the island of Hawaii,
Hawaii. This species is known from two
populations (one each in the Kohala
Mountains and Hamakua) totaling less
than 100 individuals. This species is
threatened by feral pigs and cattle,
nonnative plants, and reduced
reproductive vigor and extinction from
naturally occurring events due to small
population sizes. Because the threats
continue to be of a high magnitude and
are imminent, we retain a listing
priority number of 2 for this species.
Platydesma rostrata (Pilo kea lau
lii)—See above in ‘‘Summary of Listing
Priority Changes in Candidates.’’ The
above summary is based on information
contained in our files. No new
information was provided in the
petition received on May 11, 2004.
Pleomele forbesii (Hala pepe)—See
above in ‘‘Summary of Listing Priority
Changes in Candidates.’’ The above
summary is based on information
contained in our files. No new
information was provided in the
petition received on May 11, 2004.
Potentilla basaltica (Soldier Meadow
cinquefoil or basalt cinquefoil)—The
following summary is based on
information contained in our files. No
new information was provided in the
petition received on May 11, 2004.
Soldier Meadow cinquefoil is a lowgrowing, rhizomatous, herbaceous
perennial that is associated with alkali
meadows, seeps, and occasionally
marsh habitats bordering perennial
thermal springs, outflows, and meadow
depressions. In Humboldt County,
Nevada, the species is known only from
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. In
northeastern California, the species is
known from Ash Valley near Ash Creek
in Lassen County. In Nevada, Soldier
Meadow cinquefoil has been
documented from 10 discrete
occurrences within an area of about 70
acres that supports about 130,000
individuals. On private lands, the
population occupies less than an acre
and supports fewer than 1,000 plants.
The species and its habitat are
threatened by increasing recreational
use in the areas where the species
occurs, livestock grazing, and activities
associated with the use of authorized
and unauthorized roads. Despite the
relatively high number of individuals
observed and the apparently stable
population trend, concern over
increasing and intense recreational use
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has prompted the Service to maintain
the magnitude of threats to the species
as high. However, the threats to Soldier
Meadow cinquefoil from various land
uses are currently considered
nonimminent because of the
commitments to conservation made by
the BLM through implementation of a
regional resource management plan.
Based on this information, we are
maintaining a listing priority number of
5.
Pritchardia hardyi (Loulu)—See above
in ‘‘Summary of Listing Priority Changes
in Candidates.’’ The above summary is
based on information contained in our
files. No new information was provided
in the petition received on May 11,
2004.
Pseudognaphalium (Gnaphalium)
sandwicensium var. molokaiense
(Enaena)—See above in ‘‘Summary of
Listing Priority Changes in Candidates.’’
The above summary is based on
information contained in our files. No
new information was provided in the
petition received on May 11, 2004.
Psychotria grandiflora (Kopiko)—The
following summary is based on
information contained in our files. No
new information was provided in the
petition received on May 11, 2004.
Psychotria grandiflora is a small tree or
shrub found in mesic to sometimes wet
forest on Kauai, Hawaii. This species is
found only in the Kokee area on the
island of Kauai. The historic range of
this species was throughout Kauai’s
mesic and wet forests. While there are
no historic records of numbers of
populations or individuals, qualitative
accounts indicate that the species was
relatively widespread and abundant.
Mesic and wet forest habitats have been
significantly degraded by human
activities and natural events. Recent
surveys show that the species is now
limited to four populations, totaling 18
individuals. This species is highly
threatened by feral pigs and goats that
eat this plant and degrade and/or
destroy habitat, and nonnative plants
that compete for light and nutrients.
Because the threats continue to be of a
high magnitude and are imminent, we
retain a listing priority number of 2 for
this species.
Psychotria hexandra var. oahuensis
(Kopiko)—The following summary is
based on information contained in our
files. No new information was provided
in the petition received on May 11,
2004. Psychotria hexandra var.
oahuensis is a tree or shrub found in
mesic and wet forests on Oahu, Hawaii.
This subspecies is known from three
populations of eight individuals of the
variety oahuensis. The other varieties of
this subspecies, hoskana and rockii, are
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extinct. The historic range of this
subspecies was throughout the mesic
and wet forests on the island of Oahu.
While there are no historic records of
numbers of populations or individuals,
mesic and wet forests were once
abundant on Oahu and it is assumed
that the subspecies was relatively
widespread. This species is now
restricted to the Koolau Mountains. This
species is threatened by feral pigs that
eat it and degrade and/or destroy
habitat, and by nonnative plants that
compete for light and nutrients. Because
the threats continue to be of a high
magnitude and are imminent, we retain
a listing priority number of 3 for this
plant variety.
Psychotria hobdyi (Kopiko)—The
following summary is based on
information contained in our files. No
new information was provided in the
petition received on May 11, 2004.
Psychotria hobdyi is a tree found in
mesic forest habitat on Kauai, Hawaii.
This species is known from three
populations totaling approximately 85
individuals. This species is threatened
by feral goats that eat this plant and
degrade and/or destroy habitat,
nonnative plants that compete for light
and nutrients, reduced reproductive
vigor, and stochastic extinction due to
naturally occurring events. Because the
threats continue to be of a high
magnitude and are imminent, we retain
a listing priority number of 2 for this
species.
Pteralyxia macrocarpa (Kaulu)—See
above in ‘‘Summary of Listing Priority
Changes in Candidates.’’ The above
summary is based on information
contained in our files. No new
information was provided in the
petition received on May 11, 2004.
Ranunculus hawaiensis (Makou)—See
above in ‘‘Summary of Listing Priority
Changes in Candidates.’’ The above
summary is based on information
contained in our files. No new
information was provided in the
petition received on May 11, 2004.
Ranunculus mauiensis (Makou)—The
following summary is based on
information contained in our files. No
new information was provided in the
petition 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 Maui and Kauai,
Hawaii. Ranunculus mauiensis was
historically known from the islands of
Hawaii, Maui, Molokai, Oahu, and
Kauai. It is currently known from less
than 30 individuals on Maui and 30
individuals on Kauai. This species is
threatened by feral pigs and slugs that
eat this plant and degrade and/or
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destroy habitat, and by nonnative plants
that compete for light and nutrients.
Because the threats continue to be of a
high magnitude and are ongoing and
therefore imminent, we retain a listing
priority number of 2.
Rorippa subumbellata (Tahoe yellow
cress)—see resubmitted petition finding
published in the Federal Register on
December 27, 2004 (69 FR 77167).
Schiedea attenuata (no common
name)—The following summary is
based on information contained in our
files. No new information was provided
in the petition received on May 11,
2004. Schiedea attenuata is an erect,
sparingly branched shrub found on
cliffs in diverse mesic forest habitat on
Kauai, Hawaii. This recently discovered
species is known from one population
of less than 20 individuals on the cliffs
of Kalalau Valley. This species is
threatened by feral goats that eat this
plant and degrade and/or destroy
habitat, and by nonnative plants that
compete for light and nutrients. Because
the threats continue to be of a high
magnitude and are imminent, we retain
a listing priority number of 2 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 received on May 11, 2004.
Maolioli is a reclining or weakly
climbing vine found in diverse mesic-towet forest on Maui and Molokai,
Hawaii. Schiedea pubescens was
historically found scattered in mesic-towet forest habitat on the islands of
Molokai, Lanai, and Maui. Currently,
this species, which is declining, is
known from 6 populations totaling
approximately 100 individuals on Maui
and Molokai. This species is threatened
by feral goats that eat this plant and
degrade and/or destroy habitat, and by
nonnative plants that compete for light
and nutrients. Because the threats
continue to be of a high magnitude and
are imminent, we retain a listing
priority number of 2 for this species.
Schiedea salicaria (no common
name)—The following summary is
based on information contained in our
files. No new information was provided
in the petition received on May 11,
2004. Schiedea salicaria is an erect
subshrub or shrub found on ridges and
steep slopes in dry shrubland on Maui,
Hawaii. While there are no historic
records of numbers of populations or
individuals, qualitative accounts
indicate that this species was not
uncommon on west Maui. Currently,
this species is declining throughout its
range, and it is known from several
populations totaling 100 to 300
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individuals, typically of 25 individuals
per population. This species is
threatened by cattle that eat this plant
and degrade and/or destroy habitat, fire,
and nonnative plants that compete for
light and nutrients. Because the threats
continue to be of a high magnitude and
are imminent, we retain a listing
priority number of 2 for this species.
Sedum eastwoodiae (Red Mountain
stonecrop)—The following summary is
based on information contained in our
files. No new information was provided
in the petition received on May 11,
2004. Red Mountain stonecrop is a
perennial succulent which occupies
relatively barren, rocky openings and
cliffs in lower montane coniferous
forests which occur between 1,900 and
4,000 feet. Its distribution is limited to
Red Mountain, Mendocino County,
California, where it occupies 30 ac
scattered over 4 mi2. Total population
size is estimated as 5,300 to 23,000
plants, which occur in 27 polygons.
Intensive monitoring suggests
considerable annual variation in plant
seedling success and inflorescence
production; stonecrop density varied
from year to year. The primary threat to
the species is the potential for mining;
the species distribution overlaps a
number of mining claims, none of
which are currently active. Surface
mining, which would destroy all habitat
suitability in affected areas, would be
used to extract chromium and nickel.
The species distribution by ownership
is described as follows: Federal (Bureau
of Land Management), 95 percent; and
private, 5 percent. Given the magnitude
(high) and immediacy (nonimminent) of
the threat to the small, scattered
populations, and its taxonomy (species),
we retain a listing priority number of 5
for this species.
Sicyos macrophyllus (Anunu)—See
above in ‘‘Summary of Listing Priority
Changes in Candidates.’’ The above
summary is based on information
contained in our files. No new
information was provided in the
petition received on May 11, 2004.
Sidalcea hickmanii ssp. parishii
(Parish’s checkerbloom)—The following
summary is based on information
contained in our files and the petition
received in 1975. Parish’s checkerbloom
is known from San Bernardino, Santa
Barbara, and San Luis Obispo counties
in southern California. Two populations
occur in San Bernardino County. No
more than a dozen plants have been
found in one of these populations in the
last decade. Populations of this plant
have been reduced by habitat loss from
road construction, expansion of
recreational and communication
facilities; trampling from recreational
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activities; and grazing impacts from
cattle and wildlife. Fire suppression and
alteration of natural fire regimes are also
a potential threat to this plant. The first
location is within a 2-hour drive of 14
million people and is popular with
recreationalists. Recreational use and
development in San Bernardino
National Forest and adjacent private
inholdings continues in a manner that is
likely to preclude the opportunity to
preserve existing plants and conduct
prescribed burns to promote the
persistence of this species. The second
population of 4 individuals was recently
discovered on the north slope of the San
Bernardino Mountains the year
following a fire. This location is a
notably drier location than any of the
others found to date and expands the
model of what constitutes suitable
habitat for the species. The populations
in Santa Barbara and San Luis Obispo
Counties are more remote from
developed recreational areas. In these
locations, opportunities still exist to
conduct prescribed burns in a manner
that would promote the persistence of
this species. Because this portion of the
species’ range is exposed to less severe
threats, we conclude that the magnitude
of threat to the species as a whole is
moderate to low. Although we believe
the threat to this species is higher in the
southernmost portion of its range, the
discovery of another population there
and the potential broadening of what
might be considered suitable habitat has
slightly reduced the overall threat of
extinction of the species. Additionally,
we have new information indicating the
threat situation of Sidalcea hickmanii
ssp. parishii has improved in previous
years. However, we have not yet
completed our analysis of the current
plant information, and consequently
have not made a determination as to
whether candidate status is still
warranted in light of this new
information. We expect to complete the
analysis of the data within the next 12
months. Until we complete this
analysis, we are retaining a listing
priority number of 9 for this subspecies.
Solanum nelsonii (Popolo)—See
above in ‘‘Summary of Listing Priority
Changes in Candidates.’’ The above
summary is based on information
contained in our files. No new
information was provided in the
petition received on May 11, 2004.
Stenogyne cranwelliae (no common
name)—The following summary is
based on information contained in our
files. No new information was provided
in the petition received on May 11,
2004. Stenogyne cranwelliae is a
creeping vine found in wet forest
dominated by Metrosideros polymorpha
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on the island of Hawaii, Hawaii.
Stenogyne cranwelliae is known from 6
populations of 100 individuals.
Historically found in the Kohala
Mountains, this species was thought to
be extinct until rediscovered during
surveys of the Kohala Mountains in
1995. This species is threatened by feral
pigs and rats that eat this plant and
degrade and/or destroy habitat, and
nonnative plants that complete for light
and nutrients. Because the threats
continue to be of a high magnitude and
are imminent, we retain a listing
priority number of 2 for this species.
Stenogyne kealiae (no common
name)—The following summary is
based on information contained in our
files. No new information was provided
in the petition received on May 11,
2004. Stenogyne kealiae is a trailing or
scandent vine found in wet forest
habitat on Kauai, Hawaii. This species
is known from 5 populations totaling
100–200 individuals in the
northwestern section of the island of
Kauai. This species is threatened by
feral pigs, goats and deer that eat this
plant and degrade and/or destroy
habitat, and by nonnative plants that
complete for light and nutrients.
Because the threats continue to be of a
high magnitude and are imminent, we
retain a listing priority number of 2 for
this species.
Symphyotrichum georgianum
(Georgia aster)—The following summary
is based on information from our files.
No new information was provided in
the petition received on May 11, 2004.
Georgia aster is a relict species of post
oak savanna/prairie communities that
existed in the southeast prior to
widespread fire suppression and
extirpation of large native grazing
animals. Most populations are small,
and since the species’ main mode of
reproduction is vegetative, each isolated
population probably represents just a
few genotypes. Many populations are
threatened by woody succession due to
fire suppression, development, highway
expansion/improvement, and herbicide
application. Historically, 97 populations
of Georgia aster were known to exist; 34
of these have apparently been
destroyed. The species appears to have
been eliminated from Florida, one of the
five States in which it originally
occurred. It remains in 31 counties in 4
States (North Carolina, South Carolina,
Alabama, and Georgia). In most cases
the exact cause of extirpation was not
documented, but herbicides, highway
construction, fire suppression, and
residential and industrial development
have all altered the historic landscape in
which Georgia aster once flourished.
Most remaining populations of this
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species survive adjacent to roads,
railroads, utility rights-of-way and other
openings where land management
mimics natural disturbance regimes.
However, at these sites the species is
inherently vulnerable to accidental
destruction from herbicide application,
road shoulder grading, and other
maintenance activities. Many
populations are threatened also by
development (several are within
planned residential subdivisions),
highway expansion/improvement, and
woody succession due to fire
suppression. Two of the remaining
populations are located adjacent to
active quarries, which could eliminate
the plants as the quarries expand. One
population has been lost to competition
with kudzu (Pueraria lobata), a
nonnative plant. The threats faced by
this species are significant; however,
they continue to be nonimminent,
leading to us to retain a listing priority
number of 5 for this species.
Zanthoxylum oahuense (Ae)—The
following summary is based on
information contained in our files. No
new information was provided in the
petition received on May 11, 2004. Ae
is small tree found in mesic-to-wet
forest habitat on Oahu, Hawaii. The
historic range of Zanthoxylum oahuense
was throughout mesic or, rarely, wet
forest in the Koolau Mountains on the
island of Oahu. While there are no
historic records of numbers of
populations or individuals, qualitative
accounts indicate that the species was
not uncommon. Currently this species is
known from several populations totaling
approximately 500 individuals on Oahu.
This species is threatened by feral pigs
that eat this plant and degrade and/or
destroy habitat, the nonnative two
spotted leaf hopper that eats this plant
species, and nonnative plants that
compete for light and nutrients. Because
the threats continue to be of a high
magnitude and are imminent, we retain
a listing priority number of 2 for this
species.
Ferns and Allies
Botrychium lineare (Slender
moonwort)—The following summary is
based on information contained in our
files and the petition received on July
28, 1999. See also the 12-month petition
finding published on June 6, 2002 (67
FR 39035). The slender moonwort is
currently known from a total of 12
widely disjunct populations in 6 states:
3 in Colorado (El Paso and Lake
Counties), 1 in Idaho (Custer County), 2
in Oregon (Wallowa County), 3 in
Montana (Glacier County), 2 in Nevada
(Clark County) and 1 in Washington
(Ferry County). Historic populations,
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previously known from Idaho
(Boundary County), Montana (Lake
County), California (Fresno County),
Colorado (Boulder County), and Canada
(Quebec and New Brunswick), have not
been seen for several years and may be
extirpated. The total number of
individuals observed at the 12 extant
population sites varies, with
observations ranging from 2 to 162
individuals. Identifiable threats to
various populations of this species
include road maintenance activities,
herbicide application, recreation, timber
harvest, trampling, and development.
The slender moonwort may also be
affected by grazing from livestock or
wildlife, but specific effects of grazing
on the species are unknown. However,
if grazing by livestock or wildlife
species occurs prior to the maturation
and release of spores, the capacity for
sexual reproduction of affected plants
may be compromised.
The slender moonwort is considered
a sensitive species in Regions 2, 5, and
6 of the U.S. Forest Service, where
National Forest system lands include
extant and historical slender moonwort
sites found in Colorado, Oregon,
Washington, and California. Regional
sensitive species lists fall under Forest
Service policies that address land use
planning and management with regard
to sensitive species. Forest Service
Regions 1 and 4, which include extant
and historical sites found in Montana
and Idaho, do not have slender
moonwort on their regional sensitive
species lists and it is, therefore, not
given any special consideration by the
Forest Service in those regions.
Although the slender moonwort is
considered to be rare and imperiled by
the State Natural Heritage Programs in
Colorado, Montana, Oregon, and
Washington, the State Natural Heritage
Program rankings are not legal
designations and do not confer State
regulatory protection to this species.
Because the overall magnitude of threats
to the slender moonwort throughout its
range continues to moderate and the
overall immediacy of these threats is
nonimminent, we retain a listing
priority number of 11.
Christella boydiae (no common
name)—See above in ‘‘Summary of
Listing Priority Changes in Candidates.’’
The above summary is based on
information contained in our files. No
new information was provided in the
petition received on May 11, 2004.
Doryopteris takeuchii (no common
name)—The following summary is
based on information contained in our
files. No new information was provided
in the petition received on May 11,
2004. Doryopteris takeuchii is a small
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fern found in dry shrubland and
grassland on Oahu, Hawaii. This newly
described species is found only on the
island of Oahu on the slopes of
Diamond Head Crater in one population
totaling hundreds of individuals. It is
suspected that this species evolved
relatively recently and never had a wide
historic distribution on Oahu, but the
magnitude of the threats facing the
species has increased dramatically. This
species is threatened by nonnative
plants, fire, trampling, and erosion,
which degrade and/or destroy habitat.
Because the threats continue to be of a
high magnitude and are imminent, we
retain a listing priority number of 2 for
this species.
Huperzia stemmermanniae (no
common name)—See above in ‘‘Other
Taxonomic Changes in Candidates.’’
The above summary is based on
information contained in our files. No
new information was provided in the
petition received on May 11, 2004.
Microlepia strigosa var. mauiensis (no
common name)—See above in
‘‘Summary of Listing Priority Changes in
Candidates and Other Taxonomic
Changes in Candidates.’’ The above
summary is based on information
contained in our files. No new
information was provided in the
petition received on May 11, 2004.
Petitions To Reclassify Species Already
Listed
We previously made warranted-butprecluded findings on five petitions
seeking to reclassify threatened species
to endangered status. Because these
species are already listed, they are not
technically 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. We find that reclassification to
endangered status for the species listed
below is currently warranted but
precluded by work identified above (see
‘‘Petition Findings for Candidate
Species’’ above). In addition, these
species are currently listed as
threatened under the Act, and therefore
they 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.,
harass, harm, pursue, hunt, shoot,
wound, kill, trap, capture, or collect, or
attempt to engage in such activity).
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
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is not likely to jeopardize the continued
existence of any endangered or
threatened species.
(1) North Cascades ecosystem
population of the grizzly bear (Ursus
arctos horribilis) (Region 6) (also see 63
FR 30453, June 4, 1998, and the species
assessment form (see ADDRESSES) for
additional information on why
reclassification to endangered is
warranted-but-precluded)—Current
grizzly bear distribution has been
reduced to 5 areas in the western United
States, including the North Cascades in
north central Washington. Populations
are estimated to be fewer than 20
animals within the 9,500-square-mile
(sq-mi) (25,000-square-kilometer (sqkm)) North Cascades recovery zone.
Threats to the species in this recovery
zone include incomplete habitat
protection measures (motorized access
management) and small population size
and population fragmentation that
produce genetic isolation. We assigned
a listing priority number of 3 for this
population because of very low
population numbers as evidenced by
continuing lack of credible sightings
and little success identifying animals
through hair snagging and genetic
analysis. Information indicating
isolation of the population in British
Columbia and the United States limits
the chance of natural recovery given the
small population size. Population
augmentation may be the only way to
recover this population.
(2) Cabinet-Yaak population of the
grizzly bear (Region 6) (see also 64 FR
26725, May 17, 1999, and the species
assessment form (see ADDRESSES) for
additional information on why
reclassification to endangered is
warranted-but-precluded)—Current
grizzly bear distribution has been
reduced to 5 areas in the western United
States, including the Cabinet-Yaak in
northern Idaho and northwest Montana.
Populations are estimated to be 30–40
animals within the 2,600-sq-mi (6,700sq-km) Cabinet-Yaak recovery zone.
Threats to the species in this recovery
zone include incomplete habitat
protection measures in the form of
motorized access management,
overutilization by human-caused
mortality, and small population size and
population fragmentation that produce
genetic isolation. We assign a listing
priority number of 3 to this population
due to continuing high levels of humancaused mortality, new threats to habitat
in the form of large scale mine
development proposals in the Cabinet
Mountains, and the high potential for
further fragmentation of populations
within the recovery zone.
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(3) Selkirk grizzly population of the
grizzly bear (Region 6) (see also 64 FR
26725, May 17, 1999, and the species
assessment form (see ADDRESSES) for
additional information on why
reclassification is warranted-butprecluded)—Current grizzly bear
distribution has been reduced to 5 areas
in the western United States, including
the Selkirk Mountains in northern
Idaho, northeast Washington, and
Southeast British Columbia. Populations
are estimated to be 40–50 animals
within the 2,200 mi2 (5,700 km2) Selkirk
Mountains recovery zone. Threats to the
species in this recovery zone include
incomplete habitat protection measures
in the form of motorized access
management, overutilization in the form
of human-caused mortality, and small
population size and population
fragmentation that produce genetic
isolation. We assign a listing priority
number of 3 to this population because
of continuing high levels of humancaused mortality in British Columbia
and new genetic information indicating
the population is isolated and has
declined in genetic diversity relative to
both adjacent populations.
(4) 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 riffles with sand,
gravel, and rubble substrates, and
moderate-to-swift currents and swift
pools over sand or gravel substrates.
Specific habitat for this species consists
of shear zones where rapid flow borders
slower flow; areas of sheet flow at the
upper ends of mid-channel sand/gravel
bars; and eddies at downstream riffle
edges. Recurrent flooding and a natural
hydrograph are very important in
maintaining the habitat of spikedace
and in helping maintain a competitive
edge over invading nonnative aquatic
species.
The spikedace was once common
throughout much of the Gila River
basin, but it is now restricted to
approximately 466 km (289 mi) of
stream in portions of the upper Gila
River (Grant, Catron, and Hidalgo
Counties, NM); middle Gila River (Pinal
County, AZ); lower San Pedro River
(Pinal County, AZ); Aravaipa Creek
(Graham and Pinal Counties, AZ); Eagle
Creek (Graham and Greenlee Counties,
AZ); and the Verde River (Yavaipai
County, AZ). Its present range is only
about 10 to 15 percent of the historic
range, and the status of the species
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within occupied areas ranges from
common to very rare. The species is
now common only in Aravaipa Creek in
Arizona and some parts of the upper
Gila River in New Mexico. The
reduction in the historical distribution
of spikedace is largely attributable to the
continued modification of its habitat
and continued interactions with
nonnative species. These threats occur
over the majority of their range, to
varying degrees. Each of the individual
spikedace complexes may face unique
threats as well. For example, the San
Pedro River area is experiencing
groundwater depletion which is
affecting surface flows within the river
channel, whereas Tonto Creek faces
continued grazing pressure, recreational
use, and dewatering due to diversions.
Proposals have been made for water
exchanges affecting the Verde River in
order to provide water for growing
urban areas. Currently, threats are
exacerbated by the ongoing drought.
While some areas are subjected to fewer
disturbances or pressures, there are no
known habitat areas that are completely
free of disturbance. 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 somewhat as Federal agencies
remove cattle from streams directly, but
upland conditions continue to degrade
watersheds in general. Groundwater
withdrawals or exchanges that affect
streamflow are not reversible. Because
these high magnitude 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 are imminent. Therefore, we
assign this species a listing priority of 1
for uplisting to endangered.
(5) 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-butprecluded)—This small fish, the only
species within the genus, is found in
small-to-large perennial streams and
uses shallow, turbulent riffles with
primarily cobble substrate and swift
currents. The loach minnow uses the
spaces between, and in the lee of, larger
substrate for resting and spawning. It is
rare or absent from habitats where fine
sediments fill the interstitial spaces.
Recurrent flooding and a natural
hydrograph are very important in
maintaining the habitat of loach
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minnow and in helping the species
maintain a competitive edge over
invading nonnative aquatic species.
The loach minnow was once locally
common throughout much of the Gila
River basin, including the mainstem
Gila River upstream of Phoenix, and the
Verde, Salt, San Pedro, and San
Francisco subbasins. The present range
is only 15 to 20 percent of its historic
range, and the status of the species
within occupied areas ranges from
common to rare. The species is now
common only in Aravaipa Creek and the
Blue River in Arizona, and limited
portions of the San Francisco, upper
Gila, and Tularosa rivers in New
Mexico. The reduction in the historical
distribution of loach minnow is largely
attributable to the continued
modification of its habitat and
continued interactions with nonnative
species. These threats occur over the
majority of the range, to varying degrees.
Each of the individual loach minnow
complexes may face unique threats as
well. For example, the San Pedro River
area is experiencing groundwater
depletion which is affecting surface
flows within the river channel, whereas
Tonto Creek faces continued grazing
pressure, recreational use, and
dewatering due to diversions. Proposals
have been made for water exchanges
affecting the Verde River in order to
provide water for growing urban areas.
Currently, threats are exacerbated by the
ongoing drought. While some areas are
subjected to fewer disturbances or
pressures, there are no known habitat
areas that are completely free of
disturbance. 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 somewhat
as Federal agencies remove cattle from
streams directly, but upland conditions
continue to degrade watersheds in
general. Groundwater withdrawals or
exchanges that affect streamflow are not
reversible. Most of these highmagnitude threats to the loach minnow
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 are imminent. Therefore, we
assign this species a listing priority
number of 1 for uplisting to endangered.
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Current Notice of Review
We gather data on plants and animals
native to the United States that appear
to merit consideration for addition to
the Lists of Endangered and Threatened
Wildlife and Plants. This notice
identifies those species that we
currently regard as candidates for
addition to the Lists. These candidates
include species and subspecies of fish,
wildlife, or plants and DPSs of
vertebrate animals. This compilation
relies on information from status
surveys conducted for candidate
assessment and on information from
State Natural Heritage Programs, other
State and Federal agencies,
knowledgeable scientists, public and
private natural resource interests, and
comments received in response to
previous notices of review.
Tables 1 and 2 list animals arranged
alphabetically by common names under
the major group headings and list plants
alphabetically by names of genera,
species, and relevant subspecies and
varieties. Animals are grouped by class
or order. Plants are subdivided into two
groups: (1) Flowering plants and (2)
ferns and their allies. Useful synonyms
and subgeneric scientific names appear
in parentheses with the synonyms
preceded by an ‘‘equals’’ sign. Several
species that have not yet been formally
described in the scientific literature are
included; such species are identified by
a generic or specific name (in italics),
followed by ‘‘sp.’’ or ‘‘ssp.’’ We
incorporate standardized common
names in these notices as they become
available. We sorted 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 and
all species proposed for listing under
the Act. We emphasize that we are not
proposing these candidate species for
listing by this notice, but we anticipate
developing and publishing 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
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which we have withdrawn or finalized
the proposed rule.
PT—Species proposed for listing as
threatened.
PSAT—Species proposed for listing as
threatened due to similarity of
appearance.
C—Candidates: Species for which we
have on file sufficient information on
biological vulnerability and threats to
support proposals to list them as
endangered or threatened. Issuance of
proposed rules for these species is
precluded at present by other higherpriority 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
on Resubmitted Petitions’’ section for
additional information). We identify the
species for which we are not making a
‘‘warranted-but-precluded’’ finding on a
resubmitted petition by the code ‘‘C+’’
in the category column. We have not
updated our finding with regard to these
species since we have received
important new information that we are
currently analyzing.
The ‘‘Priority’’ column indicates the
listing priority number (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 comments or
questions (see ADDRESSES 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
species we included either as proposed
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species or as candidates in the previous
CNOR (published May 4, 2004). Since
May 4, 2004, we added two of these
species to the Lists of Endangered and
Threatened Wildlife and Plants,
withdrew one species from proposed
status, and removed five species from
candidate status for the reasons
indicated by the codes. The first column
indicates the present status of the
species, using the following codes (not
all of these codes may have been used
in this CNOR):
E—Species we listed as endangered.
T—Species we listed as threatened.
Rc—Species we removed from the
candidate list because currently
available information does not support
a proposed listing.
Rp—Species we removed from the
candidate list because we have
withdrawn the proposed listing.
The second column indicates why we
no longer regard the species as a
candidate or proposed species using the
following codes (not all of these codes
may have been used in this CNOR):
A—Species that are more abundant or
widespread than previously believed
and species that are not subject to the
degree of threats sufficient to warrant
continuing candidate status, or issuing a
proposed or final listing. The reduction
in threats could be due, in part or
entirely, to actions taken under a
conservation agreement.
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.
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;
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24927
(3) Recommending areas that we
should designate as critical habitat for a
species, or indicating that designation of
critical habitat would not be prudent for
a species;
(4) Documenting threats to any of the
included species;
(5) Describing the immediacy or
magnitude of threats facing candidate
species;
(6) Pointing out taxonomic or
nomenclature changes for any of the
species;
(7) Suggesting appropriate common
names; and
(8) Noting any mistakes, such as
errors in the indicated historical ranges.
Submit your 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. California, Hawaii, Idaho,
Nevada, 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, Oregon
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, New Mexico 87102 (505/
248–6920).
Region 3. Illinois, Indiana, Iowa,
Michigan, Minnesota, Missouri, Ohio,
and Wisconsin. Regional Director (TE),
U.S. Fish and Wildlife Service, Bishop
Henry Whipple Federal Building, One
Federal Drive, Fort Snelling, Minnesota
55111–4056 (612/713–5334).
Region 4. Alabama, Arkansas, Florida,
Georgia, Kentucky, Louisiana,
Mississippi, North Carolina, South
Carolina, Tennessee, Puerto Rico, and
the U.S. Virgin Islands. Regional
Director (TE), U.S. Fish and Wildlife
Service, 1875 Century Boulevard, Suite
200, Atlanta, Georgia 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, Massachusetts
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, Colorado 80225–0486 (303/
236–7400).
E:\FR\FM\11MYP2.SGM
11MYP2
24928
Federal Register / Vol. 70, No. 90 / Wednesday, May 11, 2005 / Proposed Rules
Region 7. Alaska. Regional Director
(TE), U.S. Fish and Wildlife Service,
1011 East Tudor Road, Anchorage,
Alaska 99503–6199 (907/786–3505).
We provided comments received in
response to the previous CNOR to the
Region having lead responsibility for
each candidate species mentioned in the
comment. We will likewise consider all
information provided in response to this
CNOR in deciding whether to propose
species for listing and when to
undertake necessary listing actions
(including whether emergency listing
pursuant to section 4(b)(7) of the Act is
appropriate). Comments we receive will
become part of the administrative record
for the species, which we maintain at
the appropriate Regional Office.
Our practice is to make comments,
including names and home addresses of
respondents, available for public
inspection. Individual respondents may
request that we withhold their home
address from the public record, which
we will honor to the extent allowable by
law. In some circumstances, we can also
withhold from the public record a
respondent’s identity, as allowable by
law. If you wish for us to withhold your
name and/or address, you must state
this request prominently at the
beginning of your comments. However,
we will not consider anonymous
comments. We will make all
submissions from organizations or
businesses, and from individuals
identifying themselves as
representatives or officials of
organizations or businesses, available
for public inspection in their entirety.
Authority
This document is published under the
authority of the Endangered Species Act
(16 U.S.C. 1531 et seq.).
Dated: May 2, 2005.
Matt Hogan,
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
Commom name
Historic range
Priority
Mammals
C* .................
3 ...............
R1
Emballonuridae ...................
Bat, Pacific sheath-tailed ....
U.S.A. (GU, CNMI).
R1
Emballonura semicaudata
rotensis.
Emballonura semicaudata
semicaudata.
C* .................
3 ...............
Emballonuridae ...................
Bat, Pacific sheath-tailed ....
6 ...............
R1
Martes pennanti ..................
Mustelidae ...........................
Fisher (west coast DPS) .....
PT ................
3 ...............
R7
Enhydra lutris kenyoni .........
Mustelidae ...........................
Otter, Northern Sea (southwest Alaska DPS).
C* .................
3 ...............
R1
Thomomys mazama couchi
Geomyidae ..........................
C* .................
3 ...............
R1
Geomyidae ..........................
C* .................
3 ...............
R1
Thomomys mazama
glacialis.
Thomomys mazama louiei ..
C* .................
3 ...............
R1
Geomyidae ..........................
C* .................
3 ...............
R1
C* .................
3 ...............
R1
C* .................
3 ...............
R1
Thomomys mazama
melanops.
Thomomys mazama
pugetensis.
Thomomys mazama
tacomensis.
Thomomys mazama tumuli
C* .................
3 ...............
R1
Geomyidae ..........................
C* .................
3 ...............
R1
Thomomys mazama
yelmensis.
Spermophilus tereticaudus
chlorus.
C* .................
9 ...............
R1
Sciuridae .............................
C* .................
5 ...............
R1
Spermophilus brunneus
endemicus.
Spermophilus washingtoni ..
Pocket gopher, Mazama
(Shelton).
Pocket gopher, Mazama
(Roy Prairie).
Pocket gopher, Mazama
(Cathlamet).
Pocket gopher, Mazama
(Olympic).
Pocket gopher, Mazama
(Olympia).
Pocket gopher, Mazama
(Tacoma).
Pocket gopher, Mazama
(Tenino).
Pocket gopher, Mazama
(Yelm).
Squirrel, Palm Springs
(=Coachella Valley)
round-tailed ground.
Squirrel, Southern Idaho
ground.
Squirrel, Washington ground
U.S.A. (AS), Fiji, Independent Samoa, Tonga,
Vanuatu.
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.
Species range: Pacific Rim
coastal waters, from
Northern Japan to Baja,
Mexico.
U.S.A. (WA).
C* .................
Geomyidae ..........................
Geomyidae ..........................
Geomyidae ..........................
Geomyidae ..........................
Sciuridae .............................
Sciuridae .............................
U.S.A. (WA).
U.S.A. (WA).
U.S.A. (WA).
U.S.A. (WA).
U.S.A. (WA).
U.S.A. (WA).
U.S.A. (WA).
U.S.A. (CA).
U.S.A. (ID).
U.S.A. (WA, OR).
Birds
C* .................
3 ...............
R1
Porzana tabuensis ..............
Rallidae ...............................
Crake, spotless (American
Samoa DPS).
C* .................
C* .................
2 ...............
3 ...............
R1
R1
Oreomystis bairdi ................
Coccyzus americanus .........
Fringillidae ...........................
Cuculidae ............................
Creeper, Kauai ....................
Cuckoo, yellow-billed (Western U.S. DPS).
C* .................
12 .............
R1
Ptilinopus perousii perousii
Columbidae .........................
Fruit-dove, many-colored ....
C* .................
6 ...............
R1
Gallicolumba stairi stairi ......
Columbidae .........................
Ground-dove, friendly .........
C* .................
6 ...............
R1
Eremophila alpestris strigata
Alaudidae ............................
Horned lark, streaked ..........
C* .................
5 ...............
R7
Brachyramphus brevirostris
Alcidae ................................
Murrelet, Kittlitz’s .................
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11MYP2
U.S.A. (AS), Australia, Fiji,
Independent Samoa, Marquesas, Philippines, Society Islands, Tonga.
U.S.A. (HI).
U.S.A. (Lower 48 States),
Canada, Mexico, Central
and South America.
U.S.A. (AS), Independent
Samoa.
U.S.A. (AS), Independent
Samoa.
U.S.A. (OR, WA), Canada
(BC).
U.S.A. (AK), Russia.
24929
Federal Register / Vol. 70, No. 90 / Wednesday, May 11, 2005 / Proposed Rules
TABLE 1.—CANDIDATE NOTICE OF REVIEW (ANIMALS AND PLANTS)—Continued
[Note: See end of SUPPLEMENTARY INFORMATION for an explanation of symbols used in this table.]
Status
Lead region
Scientific name
Family
Commom name
Alcidae ................................
Murrelet, Xantus’s ...............
U.S.A. (CA), Mexico.
R2
Synthliboramphus
hypoleucus.
Tympanuchus pallidicinctus
Phasianidae ........................
Prairie-chicken, lesser .........
6 ...............
R1
Centrocercus urophasianus
Phasianidae ........................
Sage-grouse, greater (Columbia Basin DPS).
C* .................
2 ...............
R6
Centrocercus minimus ........
Phasianidae ........................
Sage-grouse, Gunnison ......
C* .................
3 ...............
R1
Oceanodroma castro ...........
Hydrobatidae .......................
Storm-petrel, band-rumped
(Hawaii DPS).
C * ................
5 ...............
R4
Dendroica angelae ..............
Emberizidae ........................
Warbler, elfin woods ...........
U.S.A. (CO, KA, NM, OK,
TX).
U.S.A. (AZ, CA, CO, ID,
MT, ND, NE, NV, OR,
SD, UT, WA, WY), Canada (AB, BC, SK).
U.S.A (AZ, CO, KS, OK,
NM, UT).
U.S.A. (HI), Atlantic Ocean,
Ecuador (Galapagos Islands), Japan.
U.S.A. (PR).
Category
C* .................
2 ...............
R1
C* .................
8 ...............
C+ ................
Historic range
Priority
REPTILES
C * ................
C * ................
2 ...............
9 ...............
R2
R3
Sceloporus arenicolus .........
Sistrurus catenatus
catenatus.
Iguanidae ............................
Viperidae .............................
Lizard, sand dune ...............
Massasauga (= rattlesnake),
eastern.
C * ................
6 ...............
R4
Colubridae ...........................
Snake, black pine ................
C * ................
C * ................
C * ................
5 ...............
5 ...............
3 ...............
R4
R2
R2
Pituophis melanoleucus
lodingi.
Pituophis ruthveni ...............
Graptemys caglei ................
Kinosternon sonoriense
longifemorale.
U.S.A. (TX, NM).
U.S.A. (IA, IL, IN, MI, MO,
MN, NY, OH, PA, WI),
Canada.
U.S.A. (AL, LA, MS).
Colubridae ...........................
Emydidae ............................
Kinosternidae ......................
Snake, Louisiana pine ........
Turtle, Cagle’s map .............
Turtle, Sonoyta mud ...........
U.S.A. (LA, TX).
U.S.A. (TX).
U.S.A. (AZ), Mexico.
U.S.A. (AK, ID, MT, NV,
OR, UT, WA, WY), Canada (BC).
U.S.A (CA, NV).
Amphibians
C * ................
3 ...............
R1
Rana luteiventris .................
Ranidae ...............................
Frog, Columbia spotted
(Great Basin DPS).
C * ................
3 ...............
R1
Rana muscosa ....................
Ranidae ...............................
C * ................
2 ...............
R1
Rana pretiosa ......................
Ranidae ...............................
Frog, mountain yellowlegged (Sierra Nevada
DPS).
Frog, Oregon spotted ..........
C * ................
C * ................
5 ...............
3 ...............
R1
R3
Ranidae ...............................
Crytobranchidae ..................
Frog, relict leopart ...............
Hellbender, Ozark ...............
C*
C*
C*
C*
2
2
2
3
...............
...............
...............
...............
R2
R2
R2
R6
Rana onca ...........................
Cryptobranchus
alleganiensis bishopi.
Eurycea waterlooensis ........
Eurycea naufragia ...............
Eurycea chisholmensis .......
Bufo boreas boreas ............
Plethodontidae ....................
Plethodontidae ....................
Plethodontidae ....................
Bufonidae ............................
Salamander, Austin blind ....
Salamander, Georgetown ...
Salamander, Salado ...........
Toad, boreal (Southern
Rocky Mountains DPS).
11 .............
2 ...............
R1
R4
Bufo canorus .......................
Necturus alabamensis .........
Bufonidae ............................
Proteidae .............................
Toad, Yosemite ...................
Waterdog, black warrior (=
Sipsey Fork).
................
................
................
................
C * ................
C * ................
U.S.A. (CA, OR, WA), Canada (BC).
U.S.A. (AZ, NV, UT).
U.S.A. (AR, MO).
U.S.A. (TX).
U.S.A. (TX).
U.S.A. (TX).
U.S.A. (AK, CA, CO, ID,
MT, NM, OR, UT, WA,
WY), Canada (BC).
U.S.A. (CA).
U.S.A. (AL).
Fishes
PE ................
PE ................
C * ................
3 ...............
2 ...............
11 .............
R1
R2
R6
Gila bicolor vaccaceps ........
Gila intermedia ....................
Etheostoma cragini .............
Cyprinidae ...........................
Cyprinidae ...........................
Percidae ..............................
Chub, Cowhead Lake tui ....
Chub, Gila ...........................
Darter, Arkansas .................
C * ................
6 ...............
R4
Percidae ..............................
Darter, Cumberland johnny
C*
C*
C*
C*
................
................
................
................
5
5
2
3
...............
...............
...............
...............
R4
R4
R4
R6
Etheostoma nigrum
susanae.
Percina aurora .....................
Etheostoma phytophilum ....
Etheostoma moorei .............
Thymallus arcticus ..............
Percidae ..............................
Percidae ..............................
Percidae ..............................
Salmonidae .........................
C * ................
C ..................
C * ................
C * ................
C * ................
C * ................
2
5
2
5
5
3
...............
...............
...............
...............
...............
...............
R4
R4
R3
R2
R2
R2
Ictaluridae ............................
Catostomidae ......................
Cottidae ...............................
Cyprinidae ...........................
Cyprinidae ...........................
Catostomidae ......................
Darter, Pearl ........................
Darter, rush .........................
Darter, yellowcheek .............
Grayling, Fluvial arctic
(upper Missouri River
DPS).
Madtom, chucky ..................
Redhorse, sicklefin ..............
Sculpin, grotto .....................
Shiner, sharpnose ...............
Shiner, smalleye .................
Sucker, Zuni bluehead ........
PSAT ...........
N/A ...........
R1
Salmonidae .........................
Trout, Dolly Varden .............
U.S.A. (AK, WA), Canada,
East Asia.
Bean, Choctaw ....................
U.S.A. (AL, FL).
Noturus sp. ..........................
Moxostoma sp. ....................
Cottus sp. ............................
Notropis oxyrhynchus ..........
Notropis buccula .................
Catostomus discobolus
yarrowi.
Salvelinus malma ................
U.S.A. (CA).
U.S.A. (AZ, NM), Mexico.
U.S.A. (AR, CO, KS, MO,
OK).
U.S.A. (KY, TN).
U.S.A. (LA, MS).
U.S.A. (AL).
U.S.A (AR).
U.S.A. (MT, WY).
U.S.A.
U.S.A.
U.S.A.
U.S.A.
U.S.A.
U.S.A.
(TN).
(GA, NC, TN).
(MO).
(TX).
(TX).
(AZ, NM).
Clams
C ..................
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R4
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Unionidae ............................
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11MYP2
24930
Federal Register / Vol. 70, No. 90 / Wednesday, May 11, 2005 / Proposed Rules
TABLE 1.—CANDIDATE NOTICE OF REVIEW (ANIMALS AND PLANTS)—Continued
[Note: See end of SUPPLEMENTARY INFORMATION for an explanation of symbols used in this table.]
Status
Lead region
Scientific name
Family
Commom name
R3
Villosa fabalis ......................
Unionidae ............................
Bean, rayed .........................
2 ...............
R4
Unionidae ............................
Ebonyshell, round ...............
C* .................
C* .................
C ..................
C* .................
C ..................
2
5
2
5
2
...............
...............
...............
...............
...............
R2
R4
R4
R4
R3
Fusconaia (= Obovaria)
rotulata.
Popenaias popei .................
Ptychobranchus subtentum
Ptychobranchus jonesi ........
Lampsilis rafinesqueana .....
Plethobasus cyphyus ..........
Unionidae
Unionidae
Unionidae
Unionidae
Unionidae
............................
............................
............................
............................
............................
Hornshell, Texas .................
Kidneyshell, fluted ...............
Kidneyshell, southern ..........
Mucket, Neosho ..................
Mussel, sheepnose .............
C* .................
C* .................
C ..................
C* .................
C ..................
C ..................
C ..................
C ..................
2 ...............
5 ...............
5 ...............
2 ...............
5 ...............
11 .............
5 ...............
4 ...............
R4
R4
R4
R4
R4
R4
R4
R3
Margaritifera marrianae .......
Lexingtonia dolabelloides ....
Pleurobema strodeanum .....
Pleurobema hanleyanum ....
Fusconaia escambia ...........
Quincuncina burkei .............
Lampsilis australis ...............
Cumberlandia monodonta ...
Margaritiferidae ...................
Unionidae ............................
Unionidae ............................
Unionidae ............................
Unionidae ............................
Unionidae ............................
Unionidae ............................
Margaritiferidae ...................
Pearlshell, Alabama ............
Pearlymussel, slabside .......
Pigtoe, fuzzy .......................
Pigtoe, Georgia ...................
Pigtoe, narrow .....................
Pigtoe, tapered ....................
Sandshell, southern ............
Spectaclecase .....................
C* .................
5 ...............
R4
Elliptio spinosa ....................
Unionidae ............................
Spinymussel, Altamaha .......
U.S.A. (NM, TX), Mexico.
U.S.A. (AL, KY, TN, VA).
U.S.A. (AL, FL).
U.S.A. (AR, KS, MO, OK).
U.S.A. (AL, IA, IL, IN, KY,
MN, MO, MS, OH, PA,
TN, VA, WI, WV).
U.S.A. (AL)
U.S.A. (AL, KY, TN, VA)
U.S.A. (AL, FL).
U.S.A. (AL, GA, TN)
U.S.A. (AL, FL).
U.S.A. (AL, FL).
U.S.A. (AL, FL).
U.S.A. (AL, AR, IA, IN, IL,
KS, KY, MO, MN, NE,
OH, TN, VA, WI, WV).
U.S.A. (GA).
Category
C ..................
2 ...............
C ..................
Historic range
Priority
U.S.A. (IL, IN, KY, MI, NY,
OH, TN, PA, VA, WV),
Canada (ON).
U.S.A. (AL, FL).
Snails
C* .................
9 ...............
R6
Oreohelicidae ......................
Mountainsnail, Ogden .........
U.S.A. (UT)
R6
R4
Oreohelix peripherica
wasatchensis.
Stagnicola bonnevillensis ....
Leptoxis foremani(= downei)
C* .................
C* .................
8 ...............
2 ...............
Lymnaeidae .........................
Pleuroceridae ......................
U.S.A. (UT).
U.S.A. (GA, AL).
...............
...............
...............
...............
...............
...............
...............
...............
...............
...............
...............
...............
...............
...............
R1
R2
R1
R1
R1
R2
R1
R1
R1
R2
R2
R1
R2
R1
Ostodes strigatus ................
Pseudotryonia adamantina
Samoana fragilis .................
Partula radiolata ..................
Partula gibba .......................
Tryonia kosteri .....................
Partulina semicarinata .........
Partulina variabilis ...............
Partula langfordi ..................
Assiminea pecos .................
Cochliopa texana ................
Eua zebrina .........................
Pyrgulopsis chupaderae .....
Pyrgulopsis notidicola .........
Potaridae .............................
Hydrobiidae .........................
Partulidae ............................
Partulidae ............................
Partulidae ............................
Hydrobiidae .........................
Achatinellidae ......................
Achatinellidae ......................
Partulidae ............................
Assimineidae .......................
Hydrobiidae .........................
Partulidae ............................
Hydrobiidae .........................
Hydrobiidae .........................
C* .................
C* .................
11 .............
2 ...............
R2
R2
Hydrobiidae .........................
Hydrobiidae .........................
C*
C*
C*
C*
.................
.................
.................
.................
5 ...............
11 .............
5 ...............
2 ...............
R2
R2
R2
R2
Pyrgulopsis gilae .................
Tryonia circumstriata (=
stocktonensis).
Pyrgulopsis thompsoni ........
Pyrgulopsis thermalis ..........
Pyrgulopsis morrisoni ..........
Tryonia cheatumi .................
Pondsnail, Bonneville ..........
Rocksnail, Interrupted (=
Georgia).
Sisi snail ..............................
Snail, Diamond Y Spring .....
Snail, fragile tree .................
Snail, Guam tree .................
Snail, Humped tree .............
Snail, Koster’s tryonia .........
Snail, Lanai tree ..................
Snail, Lanai tree ..................
Snail, Langford’s tree ..........
Snail, Pecos assiminea .......
Snail, Phantom cave ...........
Snail, Tutuila tree ................
Springsnail, Chupadera .......
Springsnail, elongate mud
meadows.
Springsnail, Gila ..................
Springsnail, Gonzales .........
C* .................
C* .................
C* .................
C* .................
C* .................
PE ................
C* .................
C* .................
C* .................
PE ................
C* .................
C* .................
C* .................
C* .................
2
2
2
2
2
2
2
2
2
2
2
2
2
2
PE ................
C* .................
C* .................
2 ...............
2 ...............
2 ...............
R2
R2
R1
Pyrgulopsis roswellensis .....
Pyrgulopsis trivialis ..............
Newcombia cumingi ............
lHydrobiidae ........................
Hydrobiidae .........................
Achatinellidae ......................
Hydrobiidae
Hydrobiidae
Hydrobiidae
Hydrobiidae
.........................
.........................
.........................
.........................
U.S.A.
U.S.A.
U.S.A.
U.S.A.
U.S.A.
U.S.A.
U.S.A.
U.S.A.
U.S.A.
U.S.A.
U.S.A.
U.S.A.
U.S.A.
U.S.A.
(AS).
(TX).
(GU, MP).
(GU).
(GU, MP)
(NM).
(HI).
(HI).
(MP).
(NM, TX), Mexico
(TX).
(AS).
(NM).
(NV).
U.S.A. (NM).
U.S.A. (TX).
Springsnail, Huachuca ........
Springsnail, New Mexico .....
Springsnail, Page ................
Springsnail (= Tryonia),
Phantom.
Springsnail, Roswell ............
Springsnail, Three Forks .....
Tree snail, Newcomb’s ........
U.S.A.
U.S.A.
U.S.A.
U.S.A.
(AZ), Mexico
(NM).
(AZ).
(TX).
Beetle, Warm Springs
Zaitzevian riffle.
Bug, Wekiu ..........................
Butterfly, Mariana eight-spot
U.S.A. (MT).
U.S.A. (NM).
U.S.A. (AZ).
U.S.A. (Hl).
Insects
C* .................
11 .............
R6
Zaitzevia thermae ................
Elmidae ...............................
C* .................
C* .................
2 ...............
3 ...............
R1
R1
Lygaeidae ............................
Nymphalidae .......................
C* .................
2 ...............
R1
Nysius wekiuicola ................
Hypolimnas octucula
mariannensis.
Vagrans egestina ................
C * ................
6 ...............
R4
C * ................
C ..................
5 ...............
5 ...............
R4
R4
C * ................
C * ................
C ..................
5 ...............
5 ...............
11 .............
R4
R4
R4
C ..................
5 ...............
R4
VerDate jul<14>2003
17:16 May 10, 2005
Cyclargus thomasi
bethunebakeri.
Glyphopsyche sequatchie ...
Pseudanophthalmus
insularis.
Pseudanophthalmus major
Pseudanophthalmus caecus
Pseudanophthalmus
colemanensis.
Pseudanophthalmus
fowlerae.
Jkt 205001
PO 00000
Frm 00062
Nymphalidae .......................
Lycaenidae ..........................
Limnephilidae ......................
Carabidae ............................
Butterfly, Mariana wandering.
Butterfly, Miami blue ...........
U.S.A. (HI).
U.S.A. (GU, MP).
U.S.A. (GU, MP).
U.S.A. (FL), Bahamas.
Carabidae ............................
Carabidae ............................
Carabidae ............................
Caddisfly, Sequatchie .........
Cave beetle, Baker Station
(= insular).
Cave beetle, beaver ............
Cave beetle, Clifton .............
Cave beetle, Coleman ........
U.S.A. (KY).
U.S.A. (KY).
U.S.A. (TN).
Carabidae ............................
Cave beetle, Fowler’s .........
U.S.A. (TN).
Fmt 4701
Sfmt 4702
E:\FR\FM\11MYP2.SGM
11MYP2
U.S.A. (TN).
U.S.A. (TN).
24931
Federal Register / Vol. 70, No. 90 / Wednesday, May 11, 2005 / Proposed Rules
TABLE 1.—CANDIDATE NOTICE OF REVIEW (ANIMALS AND PLANTS)—Continued
[Note: See end of SUPPLEMENTARY INFORMATION for an explanation of symbols used in this table.]
Status
Lead region
Category
C * ................
5 ...............
R4
C * ................
C ..................
5 ...............
5 ...............
R4
R4
C * ................
5 ...............
R4
C * ................
5 ...............
R4
C * ................
5 ...............
R4
C ..................
C * ................
5 ...............
11 .............
R4
R4
C * ................
C * ................
5 ...............
3 ...............
R4
R1
C * ................
9 ...............
R1
C * ................
2 ...............
C * ................
Scientific name
Family
Commom name
Historic range
Pseudanophthalmus
pholeter.
Pseudanophthalmus frigidus
Pseudanophthalmus tiresias
Carabidae ............................
Cave beetle, greater Adams
U.S.A. (KY).
Carabidae ............................
Carabidae ............................
U.S.A. (KY).
U.S.A. (TN).
Pseudanophthalmus inquisitor.
Pseudanophthalmus
cataryctos.
Pseudanophthalmus troglodytes.
Pseudanophthalmus paulus
Pseudanophthalmus
inexpectatus.
Pseudanophthalmus parvus
Euphydryas editha taylori ....
Carabidae ............................
Cave beetle, icebox ............
Cave beetle, Indian Grave
Point (= Soothsayer).
Cave beetle, inquirer ...........
Carabidae ............................
Cave beetle, lesser Adams
U.S.A. (KY).
Carabidae ............................
Cave beetle, Louisville ........
U.S.A. (KY).
Carabidae ............................
Carabidae ............................
Cave beetle, Noblett’s .........
Cave beetle, surprising .......
U.S.A. (TN).
U.S.A. (KY).
Carabidae ............................
Nymphalidae .......................
Cave beetle, Tatum .............
Checkerspot, Taylor’s (=
Whulge).
Damselfly, blackline Hawaiian.
Damselfly, crimson Hawaiian.
Damselfly, flying earwig Hawaiian.
Damselfly, oceanic Hawaiian.
Damselfly, orangeblack Hawaiian.
Damselfly, Pacific Hawaiian
Gall fly, Po’olanui ................
Naucorid bug (= Furnace
Creek), Nevares Spring.
Fly, Picture wing [unnamed]
Fly, Picture wing [unnamed]
Fly, Picture wing [unnamed]
Fly, Picture wing [unnamed]
Fly, Picture wing [unnamed]
Fly, Picture wing [unnamed]
Fly, Picture wing [unnamed]
Fly, Picture wing [unnamed]
Fly, Picture wing [unnamed]
Fly, Picture wing [unnamed]
Fly, Picture wing [unnamed]
Fly, Picture wing [unnamed]
Fly, Picture wing [unnamed]
fly, Picture wing [unnamed]
Riffle beetle, Stephan’s .......
Skipper, Dakota ..................
U.S.A. (KY).
U.S.A. (OR, WA), Canada
(BC).
U.S.A. (HI).
Priority
R1
Megalagrion nigrohamatum
nigrolineatum.
Megalagrion leptodemas .....
Coenagrionidae ...................
Coenagrionidae ...................
2 ...............
R1
Megalagrion nesiotes ..........
Coenagrionidae ...................
C * ................
2 ...............
R1
Megalagrion oceanicum ......
Coenagrionidae ...................
C * ................
8 ...............
R1
Megalagrion xanthomelas ...
Coenagrionidae ...................
C * ................
C * ................
C ..................
2 ...............
5 ...............
5 ...............
R1
R1
R1
Megalagrion pacificum ........
Phaeogramma sp. ...............
Ambrysus funebris ..............
Coenagrionidae ...................
Tephritidae ..........................
Naucoridae ..........................
PE ................
C * ................
PE ................
C * ................
PE ................
PE ................
PE ................
PE ................
PE ................
PE ................
PE ................
PE ................
PE ................
PE ................
C* .................
C* .................
2 ...............
2 ...............
2 ...............
2 ...............
2 ...............
2 ...............
2 ...............
2 ...............
2 ...............
2 ...............
2 ...............
2 ...............
2 ...............
2 ...............
5 ...............
11 .............
R1
R1
R1
R1
R1
R1
R1
R1
R1
R1
R1
R1
R1
R1
R2
R3
Drosophila aglaia ................
Drosophila attigua ...............
Drosophila differens ............
Drosophila digressa ............
Drosophila hemipeza ..........
Drosophila heteroneura .......
Drosophila montgomeryi .....
Drosophila mulli ..................
Drosophila musaphila ..........
Drosophila neoclavisetae ....
Drosophila obatai ................
Drosophila ochrobasis ........
Drosophila substenoptera ...
Drosophila tarphytrichia ......
Heterelmis stephani ............
Hesperia dacotae ................
Drosophilidae ......................
Drosophilidae ......................
Drosophilidae ......................
Drosophilidae ......................
Drosophilidae ......................
Drosophilidae ......................
Drosophilidae ......................
Drosophilidae ......................
Drosophilidae ......................
Drosophilidae ......................
Drosophilidae ......................
Drosophilidae ......................
Drosophilidae ......................
Drosophilidae ......................
Elmidae ...............................
Hesperiidae .........................
C* .................
C* .................
5 ...............
9 ...............
R1
R6
Polites mardon ....................
Cicindela limbata albissima
Hesperiidae .........................
Cicindelidae .........................
C* .................
PE ................
5 ...............
3 ...............
R4
R6
Cicindela highlandensis ......
Cicindela nevadica
lincolniana.
Cicindelidae .........................
Cicindelidae .........................
Skipper, Mardon ..................
Tiger beetle, Coral Pink
Sand Dunes.
Tiger beetle, highlands ........
Tiger beetle, Salt Creek ......
U.S.A. (TN).
U.S.A. (HI).
U.S.A. (HI).
U.S.A. (HI).
U.S.A. (HI).
U.S.A. (HI).
U.S.A. (HI).
U.S.A. (CA).
U.S.A. (HI).
U.S.A. (HI).
U.S.A. (HI).
U.S.A. (HI).
U.S.A. (HI).
U.S.A. (HI).
U.S.A. (HI).
U.S.A. (HI).
U.S.A. (HI).
U.S.A. (HI).
U.S.A. (HI).
U.S.A. (HI).
U.S.A. (HI).
U.S.A. (HI).
U.S.A. (AZ).
U.S.A. (MN, IA, SD, ND, IL),
Canada.
U.S.A. (CA, OR, WA).
U.S.A. (UT).
U.S.A. (FL).
U.S.A. (NE).
Arachnids
C* .................
2 ...............
R2
Cicurina wartoni ..................
Dictynidae ...........................
Meshweaver, Warton’s cave
U.S.A. (TX).
U.S.A. (TX).
U.S.A. (NM).
U.S.A. (HI), Mozambique,
Saudi Arabia, Japan.
U.S.A. (HI), Funafuti Atoll,
Saudi Arabia, Sinai Peninsula, Tuvalu.
U.S.A. (HI).
U.S.A. (HI).
U.S.A. (HI).
U.S.A. (HI).
U.S.A. (PR), Barbuda, Dominican Republic.
CRUSTACEANS
C ..................
PE ................
C* .................
2 ...............
N/A ...........
2 ...............
R2
R2
R1
Gammarus hyalleloides .......
Gammarus desperatus .......
Antecaridina lauensis ..........
Gammaridae ........................
Gammaridae ........................
Atyidae ................................
Amphipod, diminutive ..........
Amphipod, Noel’s ................
Shrimp, anchialine pool .......
C* .................
2 ...............
R1
Calliasmata pholidota ..........
Alpheidae ............................
Shrimp, anchialine pool .......
C*
C*
C*
C*
C*
2
2
2
1
5
R1
R1
R1
R1
R4
Metabetaeus lohena ...........
Palaemonella burnsi ...........
Procaris hawaiana ..............
Vetericaris chaceorum ........
Typhlatya monae ................
Alpheidae ............................
Palaemonidae .....................
Procarididae ........................
Procaridae ...........................
Atyidae ................................
Shrimp, anchialine pool .......
Shrimp, anchialine pool .......
Shrimp, anchialine pool .......
Shrimp, anchialine pool .......
Shrimp, troglobitic groundwater.
.................
.................
.................
.................
.................
...............
...............
...............
...............
...............
Flowering Plants
C* .................
VerDate jul<14>2003
11 .............
R1
17:16 May 10, 2005
Abronia alpina .....................
Jkt 205001
PO 00000
Frm 00063
Nyctaginaceae ....................
Fmt 4701
Sfmt 4702
Sand-verbena, Ramshaw
Meadows.
E:\FR\FM\11MYP2.SGM
11MYP2
U.S.A. (CA).
24932
Federal Register / Vol. 70, No. 90 / Wednesday, May 11, 2005 / Proposed Rules
TABLE 1.—CANDIDATE NOTICE OF REVIEW (ANIMALS AND PLANTS)—Continued
[Note: See end of SUPPLEMENTARY INFORMATION for an explanation of symbols used in this table.]
Status
Lead region
Category
Scientific name
Family
Commom name
Polemoniaceae ...................
Brassicaceae .......................
Euphorbiaceae ....................
Asteraceae ..........................
Alice-flower, wonderland .....
Rockcress, Georgia .............
Silverbush, Blodgett’s ..........
Wormwood, northern ...........
U.S.A.
U.S.A.
U.S.A.
U.S.A.
(UT).
(AL, GA).
(FL).
(OR, WA).
Liliaceae ..............................
Fabaceae ............................
Fabaceae ............................
Asteraceae ..........................
Asteraceae ..........................
Pa‘iniu .................................
Milk-vetch, horseshoe .........
Milk-vetch, Sleeping Ute .....
Ko‘oko‘olau ..........................
Ko‘oko‘olau ..........................
U.S.A.
U.S.A.
U.S.A.
U.S.A.
U.S.A.
(HI).
(UT).
(CO).
(HI).
(HI).
Asteraceae ..........................
Ko‘oko‘olau ..........................
U.S.A. (HI).
Asteraceae ..........................
Asteraceae ..........................
Ko‘oko‘olau ..........................
Ko‘oko‘olau ..........................
U.S.A. (HI).
U.S.A. (HI).
Asteraceae ..........................
Poaceae ..............................
Poaceae ..............................
Mimosaceae ........................
Liliaceae ..............................
Myrtaceae ...........................
Fabaceae ............................
Fabaceae ............................
Scrophulariaceae ................
Scrophulariaceae ................
Fabaceae ............................
Brickell-bush, Florida ...........
No common name ...............
No common name ...............
No common name ...............
Mariposa lily, Siskiyou .........
No common name ..............
‘Awikiwiki .............................
‘Awikiwiki .............................
Paintbrush, Aquarius ...........
Paintbrush, Christ’s .............
Pea, Big Pine partridge .......
U.S.A.
U.S.A.
U.S.A.
U.S.A.
U.S.A.
U.S.A.
U.S.A.
U.S.A.
U.S.A.
U.S.A.
U.S.A.
Euphorbiaceae ....................
Sandmat, pineland ..............
U.S.A. (FL).
Euphorbiaceae ....................
Spurge, wedge ....................
U.S.A. (FL).
Euphorbiaceae ....................
Euphorbiaceae ....................
`
Akoko ..................................
`
Akoko ..................................
U.S.A. (HI).
U.S.A. (HI).
Euphorbiaceae ....................
`
Akoko ..................................
U.S.A. (HI).
Amaranthaceae ...................
Polygonaceae .....................
U.S.A. (HI).
U.S.A. (CA).
Asteraceae ..........................
Cactaceae ...........................
Boraginaceae ......................
Campanulaceae ..................
Campanulaceae ..................
Campanulaceae ..................
Campanulaceae ..................
Campanulaceae ..................
Campanulaceae ..................
Campanulaceae ..................
Campanulaceae ..................
Gesneriaceae ......................
Gesneriaceae ......................
Gesneriaceae ......................
Gesneriaceae ......................
Gesneriaceae ......................
Fabaceae ............................
Papala .................................
Spineflower, San Fernando
Valley.
Thoroughwort, Cape Sable
Cactus, Florida semaphore
No common name ...............
Haha ....................................
Haha ....................................
Haha ....................................
Haha ....................................
Haha ....................................
Haha ....................................
Haha ....................................
Aku ......................................
`
Haıwale ...............................
`
Haıwale ...............................
`
Haıwale ...............................
`
Haıwale ...............................
`
Haıwale ...............................
Prairie-clover, Florida ..........
U.S.A.
U.S.A.
U.S.A.
U.S.A.
U.S.A.
U.S.A.
U.S.A.
U.S.A.
U.S.A.
U.S.A.
U.S.A.
U.S.A.
U.S.A.
U.S.A.
U.S.A.
U.S.A.
U.S.A.
(FL).
(FL).
(PR), Anegada.
(HI).
(HI).
(HI).
(HI).
(HI).
(HI).
(HI).
(HI).
(HI).
(HI).
(HI).
(HI).
(HI).
(FL).
Poaceae ..............................
Poaceae ..............................
Asteraceae ..........................
Asteraceae ..........................
Panic grass, Hirsts’ .............
Crabgrass, Florida pineland
` `
Naenae ................................
` `
Naenae ................................
U.S.A.
U.S.A.
U.S.A.
U.S.A.
(DE, GA, NC, NJ).
(FL).
(HI).
(HI).
Asteraceae ..........................
Cactaceae ...........................
` `
Naenae ................................
Cactus, Acuna .....................
U.S.A. (HI).
U.S.A. (AZ), Mexico.
Asteraceae ..........................
Asteraceae ..........................
Polygonaceae .....................
Daisy, basalt .......................
Fleabane, Lemmon .............
Buckwheat, Umtanum
Desert.
Buckwheat, Churchill Narrows.
Buckwheat, Red Mountain ..
No common name ...............
Guadalupe fescue ...............
Nanu ....................................
Nohoanu ..............................
Nohoanu ..............................
Nohoanu ..............................
U.S.A. (WA).
U.S.A. (AZ).
U.S.A. (WA).
C*
C*
C*
C*
.................
.................
.................
.................
11 .............
11 .............
11 .............
3 ...............
R6
R4
R4
R1
C*
C*
C*
C*
C*
.................
.................
.................
.................
.................
2
8
8
2
3
...............
...............
...............
...............
...............
R1
R6
R6
R1
R1
C* .................
3 ...............
R1
C* .................
C* .................
8 ...............
3 ...............
R1
R1
C*
C*
C*
C*
C*
C*
C*
C*
C*
C*
C*
.................
.................
.................
.................
.................
.................
.................
.................
.................
.................
.................
8 ...............
2 ...............
2 ...............
5 ...............
5 ...............
5 ...............
2 ...............
2 ...............
8 ...............
11 .............
6 ...............
R4
R1
R1
R4
R1
R4
R1
R1
R6
R1
R4
C* .................
9 ...............
R4
C* .................
6 ...............
R4
C* .................
C* .................
2 ...............
3 ...............
R1
R1
C* .................
3 ...............
R1
C* .................
C* .................
2 ...............
6 ...............
R1
R1
C*
C*
C*
C*
C*
C*
C*
C*
C*
C*
C*
C*
C*
C*
C*
C*
C*
.................
.................
.................
.................
.................
.................
.................
.................
.................
.................
.................
.................
.................
.................
.................
.................
.................
2
2
2
2
2
2
2
2
2
2
2
2
2
2
2
2
9
...............
...............
...............
...............
...............
...............
...............
...............
...............
...............
...............
...............
...............
...............
...............
...............
...............
R4
R4
R4
R1
R1
R1
R1
R1
R1
R1
R1
R1
R1
R1
R1
R1
R4
C*
C*
C*
C*
.................
.................
.................
.................
5
5
3
3
...............
...............
...............
...............
R5
R4
R1
R1
C* .................
C* .................
2 ...............
6 ...............
R1
R2
C* .................
C* .................
C* .................
11 .............
5 ...............
2 ...............
R1
R2
R1
Aliciella cespitosa ................
Arabis georgiana .................
Argythamnia blodgettii .........
Artemisia campestris ssp.
borealis var. wormskioldii.
Astelia waialealae ...............
Astragalus equisolensis ......
Astragalus tortipes ..............
Bidens amplectens ..............
Bidens campylotheca
pentamera.
Bidens campylotheca
waihoiensis.
Bidens conjuncta .................
Bidens micrantha
ctenophylla.
Brickellia mosieri .................
Calamagrostis expansa .......
Calamagrostis hillebrandii ...
Calliandra locoensis ............
Calochortus persistens .......
Calyptranthes estremerae ...
Canavalia napaliensis .........
Canavalia pubescens ..........
Castilleja aquariensis ..........
Castilleja christii ..................
Chamaecrista lineata var.
keyensis.
Chamaesyce deltoidea
pinetorum.
Chamaesyce deltoidea
serpyllum.
Chamaesyce eleanoriae .....
Chamaesyce remyi var.
kauaiensis.
Chamaesyce remyi var.
remyi.
Charpentiera densiflora .......
Chorizanthe parryi var.
fernandina.
Chromolaena frustrata ........
Consolea corallicola ............
Cordia rupicola ....................
Cyanea asplenifolia .............
Cyanea calycina ..................
Cyanea eleeleensis .............
Cyanea kuhihewa ...............
Cyanea kunthiana ...............
Cyanea lanceolata ..............
Cyanea obtusa ....................
Cyanea tritomantha .............
Cyrtandra filipes ..................
Cyrtandra kaulantha ............
Cyrtandra oenobarba ..........
Cyrtandra oxybapha ............
Cyrtandra sessilis ................
Dalea carthagenensis
floridana.
Dichanthelium hirstii ............
Digitaria pauciflora ..............
Dubautia imbricata imbricata
Dubautia plantaginea
magnifolia.
Dubautia waialealae ............
Echinomastus erectocentrus
var. acunensis.
Erigeron basalticus ..............
Erigeron lemmonii ...............
Eriogonum codium ..............
C ..................
2 ...............
R1
Eriogonum diatomaceum ....
Polygonaceae .....................
C*
C*
C*
C*
C*
C*
C*
5 ...............
2 ...............
11 .............
2 ...............
2 ...............
8 ...............
2 ...............
R1
R1
R2
R1
R1
R1
R1
Eriogonum kelloggii .............
Festuca hawaiiensis ............
Festuca ligulata ...................
Gardenia remyi ...................
Geranium hanaense ...........
Geranium hillebrandii ..........
Geranium kauaiense ...........
Polygonaceae .....................
Poaceae ..............................
Poaceae ..............................
Rubiaceae ...........................
Geraniaceae ........................
Geraniaceae ........................
Geraniaceae ........................
.................
.................
.................
.................
.................
.................
.................
VerDate jul<14>2003
Historic range
Priority
17:16 May 10, 2005
Jkt 205001
PO 00000
Frm 00064
Fmt 4701
Sfmt 4702
E:\FR\FM\11MYP2.SGM
11MYP2
(FL).
(HI).
(HI).
(PR).
(CA, OR).
(PR).
(HI).
(HI).
(UT).
(ID).
(FL).
U.S.A (NV).
U.S.A.
U.S.A.
U.S.A.
U.S.A.
U.S.A.
U.S.A.
U.S.A.
(CA).
(HI).
(TX), Mexico.
(HI).
(HI).
(HI).
(HI).
24933
Federal Register / Vol. 70, No. 90 / Wednesday, May 11, 2005 / Proposed Rules
TABLE 1.—CANDIDATE NOTICE OF REVIEW (ANIMALS AND PLANTS)—Continued
[Note: See end of SUPPLEMENTARY INFORMATION for an explanation of symbols used in this table.]
Status
Lead region
Category
C*
C*
C*
C*
C*
C*
.................
.................
.................
.................
.................
.................
5 ...............
5 ...............
2 ...............
11 .............
5 ...............
9 ...............
R4
R1
R1
R4
R2
R4
C ..................
C* .................
C* .................
2 ...............
5 ...............
3 ...............
R6
R1
R1
C* .................
2 ...............
R1
C* .................
2 ...............
R1
C*
C*
C*
C*
C*
C*
C*
C*
C*
C*
C*
C*
C*
C*
C*
C*
C*
C*
C*
C*
.................
.................
.................
.................
.................
.................
.................
.................
.................
.................
.................
.................
.................
.................
.................
.................
.................
.................
.................
.................
2
2
2
5
2
5
5
2
3
2
2
2
2
2
2
2
2
2
2
8
...............
...............
...............
...............
...............
...............
...............
...............
...............
...............
...............
...............
...............
...............
...............
...............
...............
...............
...............
...............
R1
R1
R1
R4
R2
R4
R1
R4
R4
R1
R1
R1
R1
R1
R1
R1
R1
R1
R1
R5
C*
C*
C*
C*
.................
.................
.................
.................
2 ...............
2 ...............
11 .............
6 ...............
R1
R1
R2
R2
C* .................
C* .................
C* .................
2 ...............
2 ...............
6 ...............
R6
R6
R6
C* .................
C ..................
C* .................
C* .................
C* .................
C* .................
C* .................
C* .................
2
2
8
2
2
2
2
5
...............
...............
...............
...............
...............
...............
...............
...............
R1
R1
R6
R1
R1
R1
R1
R4
C* .................
3 ...............
R1
C* .................
3 ...............
R1
C* .................
C* .................
C ..................
C* .................
C* .................
C* .................
C* .................
2
2
2
2
5
2
3
...............
...............
...............
...............
...............
...............
...............
R1
R1
R1
R1
R1
R1
R1
C* .................
C * ................
2 ...............
3 ...............
R1
R1
C*
C*
C*
C*
C*
C*
C*
C*
2
2
2
2
8
2
2
2
R1
R1
R1
R1
R1
R1
R1
R1
................
................
................
................
................
................
................
................
VerDate jul<14>2003
Scientific name
Family
Commom name
Historic range
Gonocalyx concolor ............
Hazardia orcuttii ..................
Hedyotis fluviatilis ................
Helianthus verticillatus ........
Hibiscus dasycalyx ..............
Indigofera mucronata
keyensis.
Ipomopsis polyantha ...........
Ivesia webberi .....................
Joinvillea ascendens
ascendens.
Keysseria (= Lagenifera)
erici.
Keysseria (= Lagenifera)
helenae.
Korthalsella degeneri ..........
Labordia helleri ...................
Labordia pumila ..................
Leavenworthia crassa .........
Leavenworthia texana .........
Lesquerella globosa ............
Lesquerella tuplashensis ....
Linum arenicola ...................
Linum carteri var. carteri .....
Lysimachia daphnoides .......
Melicope christophersenii ....
Melicope degeneri ...............
Melicope hiiakae .................
Melicope makahae ..............
Melicope paniculata ............
Melicope puberula ...............
Myrsine fosbergii .................
Myrsine mezii ......................
Myrsine vaccinioides ...........
Narthecium americanum .....
Ericaceae ............................
Asteraceae ..........................
Rubiaceae ...........................
Asteraceae ..........................
Malvaceae ...........................
Fabaceae ............................
No common name ...............
Orcutt’s hazardia .................
´
Kampuaa .............................
Sunflower, whorle ................
Rose-mallow, Neches River
Indigo, Florida .....................
U.S.A.
U.S.A.
U.S.A.
U.S.A.
U.S.A.
U.S.A.
Polemoniaceae ...................
Rosaceae ............................
Joinvilleaceae ......................
Skyrocket, Pagosa ..............
Ivesia, Webber ....................
‘Ohe .....................................
U.S.A. (CO).
U.S.A. (CA, NV).
U.S.A. (HI).
Asteraceae ..........................
No common name ..............
U.S.A. (HI).
Asteraceae ..........................
No common name ...............
U.S.A. (HI).
Viscaceae ............................
Loganiaceae ........................
Loganiaceae ........................
Brassicaceae .......................
Brassicaceae .......................
Brassicaceae .......................
Brassicaceae .......................
Linaceae ..............................
Linaceae ..............................
Primulaceae ........................
Rutaceae .............................
Rutaceae .............................
Rutaceae .............................
Rutaceae .............................
Rutaceae .............................
Rutaceae .............................
Myrsinaceae ........................
Myrsinaceae ........................
Myrsinaceae ........................
Liliaceae ..............................
Hulumoa ..............................
Kamakahala ........................
Kamakahala ........................
Gladecress, unnamed .........
Gladecress, Texas golden ..
Bladderpod, Short’s ............
Bladderpod, White Bluffs ....
Flax, sand ...........................
Flax, Carter’s small-flowered
Lehua makanoe ..................
Alani ....................................
Alani ....................................
Alani ....................................
Alani ....................................
Alani ....................................
Alani ....................................
Kolea ...................................
Kolea ...................................
Kolea ...................................
Asphodel, bog .....................
Solanaceae .........................
Apocynaceae ......................
Caryophyllaceae .................
Cactaceae ...........................
‘Aiea ....................................
Holei ....................................
Whitlow-wort, bushy ............
Cactus, Fickeisen plains .....
U.S.A. (HI).
U.S.A. (HI).
U.S.A. (HI).
U.S.A. (AL).
U.S.A. (TX).
U.S.A. (IN, KY, TN).
U.S.A. (WA).
U.S.A. (FL).
U.S.A. (FL).
U.S.A. (HI).
U.S.A. (HI).
U.S.A. (HI).
U.S.A. (HI).
U.S.A. (HI).
U.S.A. (HI).
U.S.A. (HI).
U.S.A. (HI).
U.S.A. (HI).
U.S.A. (HI).
U.S.A. (DE, NC, NJ, NY,
SC).
U.S.A. (HI).
U.S.A. (HI).
U.S.A. (TX).
U.S.A. (AZ).
Scrophulariaceae ................
Scrophulariaceae ................
Scrophulariaceae ................
Beardtongue, Parachute .....
Beardtongue, Graham ........
Beardtongue, White River ...
U.S.A. (CO).
U.S.A. (CO, UT).
U.S.A. (CO, UT).
Piperaceae ..........................
Hydrophyllaceae .................
Hydrophyllaceae .................
Lamiaceae ...........................
Lamiaceae ...........................
Lamiaceae ...........................
Pittosporaceae ....................
Orchidaceae ........................
‘Ala ‘ala wai nui ...................
Brand’s phacelia .................
Phacelia, DeBeque .............
No common name ..............
No common name ...............
No common name ...............
Ho‘awa ................................
Orchid, white fringeless .......
Rutaceae .............................
No common name ...............
U.S.A. (HI).
U.S.A. (CA), Mexico.
U.S.A. (CO).
U.S.A. (HI).
U.S.A. (HI).
U.S.A. (HI).
U.S.A. (HI).
U.S.A. (AL, GA, KY, MS,
NC, SC, TN, VA).
U.S.A. (HI).
Rutaceae .............................
No common name ...............
U.S.A. (HI).
Rutaceae .............................
Rutaceae .............................
Agavaceae ..........................
Agavaceae ..........................
Rosaceae ............................
Asteraceae ..........................
Asteraceae ..........................
No common name ..............
Pilo kea lau li‘i .....................
Hala pepe ............................
Hala pepe ............................
Cinquefoil, Soldier Meadow
Lo‘ulu ...................................
‘Ena‘ena ..............................
U.S.A.
U.S.A.
U.S.A.
U.S.A.
U.S.A.
U.S.A.
U.S.A.
Rubiaceae ...........................
Rubiaceae ...........................
Kopiko .................................
Kopiko .................................
U.S.A. (HI).
U.S.A. (HI).
Rubiaceae ...........................
Apocynaceae ......................
Ranunculaceae ...................
Ranunculaceae ...................
Brassicaceae .......................
Caryophyllaceae .................
Caryophyllaceae .................
Caryophyllaceae .................
Kopiko .................................
Kaulu ...................................
Makou .................................
Makou .................................
Cress, Tahoe yellow ...........
No common name ..............
Ma‘oli‘oli ...............................
No common name ..............
U.S.A.
U.S.A.
U.S.A.
U.S.A.
U.S.A.
U.S.A.
U.S.A.
U.S.A.
Priority
...............
...............
...............
...............
...............
...............
...............
...............
17:16 May 10, 2005
Nothocestrum latifolium .......
Ochrosia haleakalae ...........
Paronychia congesta ...........
Pediocactus peeblesianus
fickeiseniae.
Penstemon debilis ...............
Penstemon grahamii ...........
Penstemon scariosus var.
albifluvis.
Peperomia subpetiolata ......
Phacelia stellaris .................
Phacelia submutica .............
Phyllostegia bracteata .........
Phyllostegia floribunda ........
Phyllostegia hispida ............
Pittosporum napaliense .......
Platanthera integrilabia .......
Platydesma cornuta var.
cornuta.
Platydesma cornuta var.
decurrens.
Platydesma remyi ................
Platydesma rostrata ............
Pleomele fernaldii ...............
Pleomele forbesii .................
Potentilla basaltica ..............
Pritchardia hardyi ................
Pseudognaphalium
(=Gnaphalium)
sandwicensium var.
molokaiense.
Psychotria grandiflora .........
Psychotria hexandra var.
oahuensis.
Psychotria hobdyi ................
Pteralyxia macrocarpa ........
Ranunculus hawaiensis ......
Ranunculus mauiensis ........
Rorippa subumbellata .........
Schiedea attenuata .............
Schiedea pubescens ...........
Schiedea salicaria ...............
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(PR).
(CA), Mexico
(HI).
(AL, GA, TN).
(TX).
(FL).
(HI).
(HI).
(HI).
(HI).
(NV).
(HI).
(HI).
(HI).
(HI).
(HI).
(HI).
(CA, NV).
(HI).
(HI).
(HI).
24934
Federal Register / Vol. 70, No. 90 / Wednesday, May 11, 2005 / Proposed Rules
TABLE 1.—CANDIDATE NOTICE OF REVIEW (ANIMALS AND PLANTS)—Continued
[Note: See end of SUPPLEMENTARY INFORMATION for an explanation of symbols used in this table.]
Status
Lead region
Category
Scientific name
Family
Commom name
Historic range
Crassulaceae ......................
Cucurbitaceae .....................
Malvaceae ...........................
Sapotaceae .........................
Stonecrop, Red Mountain ...
‘Anunu .................................
Checkerbloom, Parish’s ......
Bully, Everglades ................
U.S.A.
U.S.A.
U.S.A.
U.S.A.
Solanaceae .........................
Asteraceae ..........................
Lamiaceae ...........................
Lamiaceae ...........................
Asteraceae ..........................
Popolo .................................
Goldenrod, Yadkin River .....
No common name ...............
No common name ..............
Aster, Georgia .....................
Rutaceae .............................
A‘e .......................................
U.S.A. (HI).
U.S.A. (NC)
U.S.A. (HI).
U.S.A. (HI).
U.S.A. (AL, FL, GA, NC,
SC).
U.S.A. (HI).
Priority
C * ................
C * ................
C * ................
C ..................
5
2
9
9
...............
...............
...............
...............
R1
R1
R1
R4
C * ................
C ..................
C * ................
C * ................
C * ................
2
8
2
2
5
...............
...............
...............
...............
...............
R1
R4
R1
R1
R4
C * ................
2 ...............
R1
Sedum eastwoodiae ...........
Sicyos macrophyllus ...........
Sidalcea hickmanii parishii ..
Sideroxylon reclinatum ssp.
austrofloridense.
Solanum nelsonii .................
Solidago plumosa ...............
Stenogyne cranwelliae ........
Stenogyne kealiae ..............
Symphyotrichum
georgianum.
Zanthoxylum oahuense .......
(CA).
(HI).
(CA).
(FL).
C * ................
11 .............
R1
Botrychium lineare ..............
Ophioglossaceae ................
Moonwort, slender ..............
C * ................
2 ...............
R1
Thelypteridaceae .................
No common name ...............
C * ................
C * ................
2 ...............
2 ...............
R1
R1
Pteridaceae .........................
Lycopodiaceae ....................
No common name ...............
Wawae‘iole ..........................
U.S.A. (HI).
U.S.A. (HI).
C * ................
3 ...............
R1
Christella boydiae (=
Cyclosorus boydiae var.
boydiae + Cyclosorus
boydiae kipahuluensis).
Doryopteris takeuchii ...........
Huperzia (= Phlegmariurus)
stemmermanniae.
Microlepia strigosa var.
mauiensis (= Microlepia
mauiensis).
U.S.A. (CA, CO, ID, MT,
OR, WA), Canada (AB,
BC, NB, QC).
U.S.A. (HI).
Dennstaedtiaceae ...............
Palapali ...............................
U.S.A. (HI).
Ferns and Allies
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
Code
Scientific name
Family
Commom name
Historic range
Expl.
Mammals
T ...................
L ...............
R1
Pteropus mariannus
mariannus.
Pteropodidae .......................
Rc ................
A ..............
6
Cynomys ludovicianus ........
Sciuridae .............................
Bat, Mariana fruit (= Mariana flying fox) (Aguijan,
etc.).
Prairie dog, black-tailed ......
Western Pacific Ocean,
U.S.A. (GU, MP).
U.S.A. (AZ, CO, KS, MT,
NE, NM, ND, OK, SD,
TX, WY), Canada, Mexico.
Amphibians
T ...................
L ...............
R1
Ambystoma californiense ....
Ambystomatidae .................
Salamander, California tiger
U.S.A. (CA).
Clubshell, Alabama .............
Clubshell, painted ...............
U.S.A. (AL, GA, TN).
U.S.A. (AL, GA, TN).
Butterfly, Sacramento
Mountains checkerspot.
Cave Beetle, Holsinger’s .....
U.S.A. (NM).
Clams
Rc ................
Rc ................
N ..............
N ..............
R4
R4
Pleurobema troschelianum
Pleurobema
chattanoogaense.
Unionidae ............................
Unionidae ............................
Insects
Rp ................
A ..............
R2
Nymphalidae .......................
R5
Euphydryas anicia
cloudcrofti.
Pseudanophthalmus
holsingeri.
Rc ................
A ..............
Rc ................
A ..............
R4
Fallicambarus gordoni .........
Cambaridae .........................
Carabidae ............................
U.S.A. (VA).
Crustaceans
Crayfish, Camp Shelby burrowing.
[FR Doc. 05–9283 Filed 5–5–05; 1:01 pm]
BILLING CODE 4310–55–P
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17:24 May 10, 2005
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U.S.A. (MS).
Agencies
[Federal Register Volume 70, Number 90 (Wednesday, May 11, 2005)]
[Proposed Rules]
[Pages 24870-24934]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 05-9283]
[[Page 24869]]
-----------------------------------------------------------------------
Part II
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 or Proposed 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. 70, No. 90 / Wednesday, May 11, 2005 /
Proposed Rules
[[Page 24870]]
-----------------------------------------------------------------------
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 or Proposed 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
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 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 to each species. 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.
We request additional status information that may be available for
the 286 candidate species. 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 that we should include as
candidates as we prepare future updates of this list.
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 May 5, 2004, through
May 2, 2005.
DATES: We will accept comments on the Candidate Notice of Review at any
time.
ADDRESSES: Submit your comments regarding a particular species to the
Regional Director of the Region identified in SUPPLEMENTARY INFORMATION
as having the lead responsibility for that species. You may submit
comments of a more general nature to the Chief, Division of
Conservation and Classification, U.S. Fish and Wildlife Service, 4401
N. Fairfax Drive, Room 420, Arlington, VA 22203 (703/358-2171). Written
comments and materials received in response to this notice will be
available for public inspection by appointment at the Division of
Conservation and Classification (for comments of a general nature only)
or at the appropriate Regional Office listed in SUPPLEMENTARY
INFORMATION.
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
Division of Conservation and Classification, Arlington, Virginia (see
address above), or on our Internet Web site (https://endangered.fws.gov/
candidates/).
FOR FURTHER INFORMATION CONTACT: The Endangered Species Coordinator(s)
in the appropriate Regional Office(s) or Chris Nolin, Chief, Division
of Conservation and Classification (703-358-2171).
SUPPLEMENTARY INFORMATION:
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. Through the Federal rulemaking
process, we add these species to the List of Endangered and Threatened
Wildlife at 50 CFR 17.11 or the List of Endangered and Threatened
Plants at 50 CFR 17.12. As part of this program, we maintain a list of
species that we regard as candidates for listing. A candidate species
is one for which we have on file sufficient information on biological
vulnerability and threats to support a proposal to list as endangered
or threatened, but for which preparation and publication of a proposal
is precluded by higher-priority listing actions. We maintain this list
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
conservation efforts that will remove or reduce threats to these
species; to solicit 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
solicit necessary information for setting priorities for preparing
listing proposals.
Table 1 includes 286 species that we regard as candidates for
addition to the Lists of Endangered and Threatened Wildlife and Plants
(Lists), as well as 21 species for which we have published proposed
rules to list as threatened or endangered species. Most of these
proposed species were previously identified in the 2003 CNOR (69 FR
24876, May 4, 2004). We encourage consideration of these species in
conservation planning, as well as other environmental planning, such as
in environmental impact analysis done under the National Environmental
Policy Act of 1969 (implemented at 40 CFR parts 1500-1508) and in local
and statewide land use planning. Table 2 contains eight species we
identified as candidates or as proposed species in the May 4, 2004,
CNOR that we now no longer consider candidates. This includes two
species that we listed as threatened since May 4, 2004, one species
that we withdrew the proposed rule, one species that we removed from
candidacy through a notice published on August 18, 2004 (69 FR 51217),
and four species that we are removing from candidacy through this
notice. The Region having lead responsibility for the particular
species maintains updated records of information on candidate species.
Previous Notices of Review
The Act directed the Secretary of the Smithsonian Institution to
prepare a report on endangered and threatened plant species, which was
published as House Document No. 94-51. We published a notice in the
Federal Register on July 1, 1975 (40 FR 27823), in which we announced
that we would review more than 3,000 native plant species named in the
Smithsonian's report and other species added by the 1975 notice for
possible addition to the List of Endangered and Threatened Plants. A
new comprehensive notice of review for native plants, which took into
account the earlier Smithsonian
[[Page 24871]]
report and other accumulated information, superseded the 1975 notice on
December 15, 1980 (45 FR 82479). On November 28, 1983 (48 FR 53640), a
supplemental plant notice of review announced changes in the status of
various species. We published complete updates of the plant notice on
September 27, 1985 (50 FR 39526); February 21, 1990 (55 FR 6184);
September 30, 1993 (58 FR 51144); and, as part of combined animal and
plant notices, on February 28, 1996 (61 FR 7596); September 19, 1997
(62 FR 49398); October 25, 1999 (64 FR 57534); October 30, 2001 (66 FR
54808); June 13, 2002 (67 FR 40657); and May 4, 2004 (69 FR 24876).
Additionally, on January 8, 2001 (66 FR 1295), we published our
resubmitted petition finding for one plant species having an
outstanding ``warranted-but-precluded finding'' on a petition to list.
We published earlier comprehensive reviews for vertebrate animals
in the Federal Register on December 30, 1982 (47 FR 58454), and on
September 18, 1985 (50 FR 37958). We published an initial comprehensive
review for invertebrate animals on May 22, 1984 (49 FR 21664). We
published a combined animal notice of review on January 6, 1989 (54 FR
554), and with minor corrections on August 10, 1989 (54 FR 32833). We
again published comprehensive animal notices on November 21, 1991 (56
FR 58804); November 15, 1994 (59 FR 58982); and, as part of combined
animal and plant notices, on February 28, 1996 (61 FR 7596); September
19, 1997 (62 FR 49398); October 25, 1999 (64 FR 57534); October 30,
2001 (66 FR 54808); June 13, 2002 (67 FR 40657); and May 4, 2004 (69 FR
24876). Additionally, on January 8, 2001 (66 FR 1295), we published our
resubmitted petition findings for 25 animal species having outstanding
``warranted-but-precluded'' petition findings as well as notice of one
candidate removal.
This revised notice supersedes all previous animal, plant, and
combined notices of review.
Summary
Since publication of the 2003 CNOR on May 4, 2004 (69 FR 24876), we
reviewed the available information on candidate species to ensure that
a proposed listing is justified for each species and reevaluated the
relative listing priority assignment of each species. A candidate
species is assigned a listing priority number (LPN) of 1-12 depending
on the magnitude of threats, the imminence of threats, and by its
taxonomic status in accordance with our priority guidance as published
on September 21, 1983 (48 FR 43098). We also evaluated the need to
emergency-list any of these species, particularly species with high
priorities (i.e., species with listing priority numbers of 1, 2, or 3).
This review and reevaluation ensures that we focus conservation efforts
on those species at greatest risk. As of May 2, 2005, 18 animals are
proposed for endangered status; 2 animals are proposed for threatened
status (not including proposed reclassifications of endangered
species); 1 animal is proposed for threatened-due-to-similarity-of-
appearance status; and 145 plant and 141 animal candidates are awaiting
preparation of proposed rules (see Table 1). Table 2 includes eight
species we previously classified as either proposed for listing or
candidates that we no longer classify in those categories.
Summary of New Candidates
Below we present brief summaries of five new candidates, including
one species of fish, one insect, one crustacean, and two plants.
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
Web site (https://endangered.fws.gov/candidates/).
Fish
Sicklefin redhorse (Moxostoma sp.)--The sicklefin redhorse is a
medium-sized redhorse fish, reaching up to about 18 inches, with an
elongate, somewhat compressed body and a highly falcate (sickle-shaped)
dorsal fin and are found in North Carolina, Tennessee and Georgia.
Detailed morphological and genetic studies have concluded that the
sicklefin redhorse is a distinct species. The species is currently
known to occupy cool to warm, moderate gradient creeks and rivers, and,
during parts of its early life stages, large reservoirs. In streams, it
is most often observed in riffles, runs, and well-flowing pools. It
feeds and spawns in gravel, cobble, and boulder substrates with no, or
very little, silt overlay.
Like many other redhorse species, the sicklefin redhorse is known
mainly from flowing streams; however, also like many other redhorse
species, the sicklefin redhorse appears to have adapted to spending at
least part of its life in the near-shore areas of impounded streams
where pre-spawning age sicklefins have been collected, mainly near the
mouth of streams that feed the reservoirs. Current observations
indicate that adults of the species are year-round residents of rivers
and large creeks and that young, juveniles, and subadults occupy
primarily the lower reaches of creeks and rivers and near-shore
portions of certain reservoirs. It is likely that after emerging from
the stream substrata, many of the larvae and postlarvae are carried
downstream to the mouths of streams or into reservoirs. Newly mature
fish (>=5 years of age) appear to migrate from the reservoirs to spawn
and then remain in the streams with the other adults.
Based on an analysis of preserved specimens, the species is
relatively long lived, with both sexes living at least to 17 years of
age; however, based on the size of fish seen in the streams, some
individuals probably live for over 20 years. Spawning typically occurs
over cobble, with usually only a small portion of sand and gravel, in
moderate to fast runs in open areas and pockets formed by boulders and
outcrops. The spawning period for the sicklefin runs from late April
through mid-May.
Past and recent collection records of the sicklefin redhorse,
together with what is known about the habitat utilization of the
species, indicate that the sicklefin redhorse once inhabited the
majority, if not all, of the rivers and large creeks in the Blue Ridge
portion of the Hiwassee and Little Tennessee River systems in North
Carolina, Tennessee, and Georgia. Current estimates are that the
species has apparently been eliminated from roughly 60 percent of its
former range. This is a conservative estimate that: (1) Includes
several miles of the Hiwassee and Fontana Reservoirs within the present
range of the species (although portions of these reservoirs appear to
provide survivable habitat for juvenile sicklefins, they do not provide
foraging or spawning habitat for adults of the species); and (2) does
not include some of the higher reaches of some of the creeks where the
sicklefin redhorse currently occurs in their lowermost reaches.
Additionally, the Cheoah River, Cullasaja River, Cartoogechaye Creek,
Oconaluftee River, and several other large tributaries in the Hiwassee
and Little Tennessee River systems may also have once been inhabited by
the sicklefin redhorse.
Impacts associated with the construction and operation of dams for
hydropower generation on the streams inhabited by the species is the
primary cause of the extirpation of the sicklefin redhorse throughout
the majority of its former range. These impoundments created by the
dams eliminate spawning and foraging habitat of the adult sicklefin
redhorse by changing the conditions from flowing to still water.
[[Page 24872]]
Water depth increases, flow decreases, and silt accumulates on the
bottom. Impoundments not only destroy riverine habitat within the
impounded portion of the stream, but they alter the quality and
stability of the downstream reaches by adversely affecting water flow
regimes, velocities, temperature, chemistry, and nutrient cycles. Dams
that operate by releasing cold water from near the bottom of the
reservoirs lower the water temperature downstream, changing downstream
reaches from warm-or cool-water streams to cold-water streams and
affecting their suitability for many of the native species historically
inhabiting these stream reaches. The effects of impoundments result in
changes in fish and macroinvertebrate communities (macroinvertebrates
are the main prey items of the sicklefin), species requiring clean
gravel and sand substrates are lost. In addition, dams result in the
fragmentation and isolation of populations of remaining populations of
the sicklefin redhorse, acting as effective barriers to the natural
upstream and downstream expansion or recruitment of the species.
Natural upstream and downstream population expansion and repopulation
of the majority of the species' former range are restricted because of
the barriers posed by the existing dams and impacts to the tailwaters
associated with the current operation of the dams. As a result, the
Hiwassee River system and Little Tennessee River system populations are
isolated from each other. This isolation decreases their ability to
respond to nature- and human-induced changes in their environment and
increases their vulnerability to extirpation. Wastewater discharges,
together with impacts to water and habitat quality associated with a
variety of other land disturbance activities carried out without
adequate measures to control storm water and erosion, also played a
significant role in the decline of the species.
Many of the same factors believed to have contributed to the
extirpation of the species from much of its former range potentially
threaten these remaining populations. All of the surviving occurrences
of the sicklefin redhorse are restricted to relatively short reaches of
the streams they occupy, primarily due to existing dams. Their limited
distributions make them extremely vulnerable to the effects from single
catastrophic events (such as toxic chemical spills, major sedimentation
events, channel modification, etc.) and/or the cumulative effects of
lesser impacts to their habitat and numbers. Although the majority of
the streams still occupied by the species occur in areas that are
presently primarily rural, many of the communities within the
watersheds of these streams are experiencing increasing development
pressure, both commercial and residential, and are developing plans for
upgrading and improving their infrastructure (e.g., roads, water
supplies, sewer/wastewater treatment systems, etc.) to provide for
increased densities of development.
Because of the entire current range of the sickelefin redhorse is
affected by the threats described above, the magnitude of the threat to
the species is high. Although the threats faced by the sicklefin
redhorse are significant, it is not anticipated that the species will
be subject to these threats in the immediate future. Therefore, we
assigned a listing priority of 5 to this species.
Insects
Miami blue butterfly (Cyclargus thomasi bethunebakeri)--The Miami
blue is a coastal butterfly that occurs at the edges of tropical
hardwood hammocks (forests) and occasionally in tropical pinelands and
along trails, utilizing open sunny areas in southern Florida. The
geographic range of this butterfly once extended from the Florida Keys
north along the coasts to about St. Petersburg and Daytona, Florida.
Although little specific historic information exists on the abundance
and distribution patterns of the Miami blue, it is clear that the
occurrence of this butterfly throughout its historic range has been
significantly reduced, with only small remnants remaining. Despite
extensive surveys of known suitable habitat and/or historical records,
the species is now found only in a single metapopulation, located at
Bahia Honda Key State Park (Park), with a few immature individuals on
West Summerland Key. This metapopulation is comprised of thirteen
distinct colonies in the Park.
In November 2002, the Service worked with researchers and the State
to establish a captive propagation program for the Miami blue due to
the low estimated population at its only known location. As of December
2004, the captive colony had numerous generations, with hundreds of
individuals in captivity. Efforts have been undertaken to reintroduce
captive-bred Miami blues to Federal lands (i.e., Everglades National
Park and Biscayne National Park) within the butterfly's historic range.
However, subsequent monitoring has indicated an inconsistent or
sporadic presence of only a small number of individuals of varying life
stages at release sites. Monitoring results do not indicate that the
Miami blue has become established at any of the release sites.
Extensive losses of the species' habitat and fragmentation of
remaining patches, along with mosquito control activities, are the
likely cause of the species' decline. Although many areas on public
lands may offer suitable nectar and other host plants, the extremely
limited dispersal ability of the species likely prevents these areas
from becoming occupied and used. The Miami blue butterfly is threatened
by the combined influences of habitat destruction and modification,
mosquito control activities, and loss of genetic diversity associated
with isolated populations. The possibility for catastrophic events
(e.g., hurricanes) also poses a threat to the survival of this
butterfly. In addition to these threats, habitat loss and
fragmentation, fire suppression, displacement of native host plants by
invasive exotic species, detrimental land management practices,
accidental harm from humans, and inadequate regulatory protection pose
threats to the species throughout the species historic range.
Predation, accidental harm or habitat destruction, and illegal
collection may also pose a threat to the Miami blue due to the small
population size at the known locations. Due to nonimminent threats of
high magnitude as described above, we assigned a listing priority
number of 6 to this subspecies.
Crustaceans
Diminutive amphipod (Gammarus hyalleloides)--The diminutive
amphipod is a small amphipod that is ranked as ``critically endangered
throughout its range'' (G1) by NatureServe and ``critically endangered
throughout its range'' (S1) by the State of Texas. Based on surveys and
genetic analysis, this species only occurs in four spring outflows in
the Toyah Basin, Balmorhea area of Reeves and Jeff Davis Counties,
Texas; these springs are all within about 8 miles (13 km) of each other
within the San Solomon Spring System. In addition to being an important
habitat for rare aquatic fauna, this spring system is also an important
source of irrigation water for the farming communities in the Toyah
Basin. The primary threat to the species is the loss of surface flows
due to declining groundwater levels from drought and pumping for
agricultural production. The natural ci[egrave]nega habitats (marshland
communities associated with perennial springs and headwater streams) of
the Balmorhea area have been mostly altered over time to accommodate
agricultural irrigation. Most significant was the draining of wetland
areas and the modification of spring outlets for
[[Page 24873]]
development of human use of the water resources. Although the land
surrounding the amphibod's current habitat is owned and managed by The
Nature Conservancy, Bureau of Reclamation, and Texas Parks and Wildlife
Department, the water needed to maintain its habitat has declined due
to a reduction in spring flows, possibly as result of private
groundwater pumping in areas beyond that are controlled by these
landowners. Pumping of the regional aquifer system for agricultural
production of crops has resulted in the drying of other springs in this
region, including Comanche Springs, which was once a large surface
spring in Fort Stockton, Texas. Another example is Phantom Lake Spring,
one of the sites of occurrence for the amphipod, which ceased flowing
in 2000; aquatic habitat is now supported only by a pumping system.
Another threat to amphipod habitat is the potential degradation of
water quality from point and nonpoint pollutant sources. This pollution
can occur either directly into surface water or indirectly through
contamination of groundwater that discharges into spring run habitats
used by the amphipod. The primary threat for contamination comes from
herbicide and pesticide use in nearby agricultural areas.
Although the physical condition of the areas where this species is
found has changed dramatically over time from human actions, at least a
portion of the native biota remain. However, three of the four known
current occurrences of the species are in degraded habitats (the
exception is East Sandia Spring) because the natural conditions of the
springs have been substantially modified for human use. Any additional
modifications to the spring flow habitats will further threaten the
species. Therefore, with imminent threats of high magnitude, we assign
this species a listing priority number of 2.
Flowering Plants
Ipomopsis polyantha (Pagosa skyrocket)--Pagosa skyrocket is an
extremely narrow endemic with a global distribution limited to a 13-
mile range on outcrops of Pagosa-Winifred soils derived from mancos
shale in Archuleta County, Colorado. The total population size is
estimated to be between 2,246 and 10,626 plants. It is ranked as
``critically endangered throughout its range'' (G1) by NatureServe and
``critically endangered in the state'' (S1) by the Colorado Natural
Heritage Program. Populations are on federal highway rights of way and
private lands. Much of the occupied habitat on private lands has been
subdivided and is being rapidly developed. There are no plans being
implemented for the management, protection, or conservation of the
species. The Colorado Rare Plant Technical Committee, including
botanists from the Colorado Natural Heritage Program, has identified I.
polyantha as the species most in need of protection and recovery
efforts in 2005 in Colorado. We assign this species a listing priority
number 2 based on imminent habitat destruction throughout its narrow
range.
Solidago plumosa (Yadkin River goldenrod)--A member of the
Asteraceae family, Solidago plumosa is endemic to the Yadkin River in
North Carolina and was originally described from the Narrows Canyon and
Falls area of this river in 1894. Currently, plants are know to exist
in only two locations, located approximately 2 kilometers apart along
the shoreline of the Yadkin River in North Carolina. This species is
ranked as ``critically endangered throughout its range'' (G1) by
NatureServe and ``critically endangered in the state'' (S1) by the
North Carolina Natural Heritage Program. The historical and current
impacts resulting from the construction and operation of reservoirs
appear to be similar at each of these two surviving occurrences of the
species, as does the threat posed by invasive, nonnative vegetation.
The species appears to persist in areas subjected to periodic water
scouring of a velocity sufficient to prevent the establishment of other
species without eliminating previously established Solidago plumosa
plants (the age of which is unknown). At the same time, although
dependent upon some level of flood scouring, the species does not
appear to be tolerant of prolonged inundation as it does not occur in
frequently flooded habitats. Therefore, the availability of suitable
habitat and the fate of all known populations of this species are
primarily determined by the manner in which the Narrows and Falls
Reservoirs are operated. To the extent that operation of hydroelectric
facilities could be modified in the future to enhance conditions for
Solidago plumose, the effects of reservoir construction and operation
are not believed to be permanent or irreversible. Thus, the magnitude
of these threats may be substantially reduced. In light of all of these
considerations, the magnitude of threats to the species is estimated to
be ``moderate to low.''
One of the primary threats that affected the species (construction
of Narrows and Falls Reservoirs and the resulting inundation of
suitable habitat) has already occurred. However, operation of these
reservoirs continues to influence the habitat occupied by the species,
and may be facilitating (via a reduction in the frequency and magnitude
of scouring events) the establishment and spread of mimosa (Albizia
julibrissin) (an invasive, nonnative shrub). Because mimosa is already
shading established Solidago plumosa plants, it may potentially be
competing for seed germination and seedling establishment sites. The
threats posed by lack of scouring and the subsequent establishment and
spread of mimosa are ongoing and, therefore, considered to be imminent.
The threat posed by the nonnative hybrid bush honeysuckle (Lonicera x
bella) is more remote, as the species has not yet established in
habitats occupied by Solidago plumosa. We conclude that the threats
affecting the species are of a moderate to low magnitude, but are
imminent, leading to a listing priority number of 8.
Summary of Listing Priority Changes in Candidates
We reviewed the listing priority number for all candidate species
and are changing the numbers for the following species. Some of the
changes reflect actual changes in either the magnitude or imminence of
the threats, and in two cases, reflect a change in the taxonomy of the
species. For some species, our changes in the listing priority number
reflect efforts to ensure national consistency as well as closer
adherence to the 1983 guidelines in assigning these numbers, rather
than a change in the nature of the threats.
Mammals
Mazama pocket gopher (Thomomys mazama ssp. couchi, glacialis,
louiei, melanops, pugetensis, tacomensis, tumuli, and yelmensis)--
Candidate status applies to each of these eight subspecies of Thomomys
mazama, all of which are associated with glacial outwash prairies in
western Washington. We do not include other T. mazama subspecies that
occur in Oregon and California (commonly referred to as ``western
pocket gophers'') as candidate species. Except as otherwise noted, the
following description applies to each of the subspecies. Most
populations are small, isolated, and patchily distributed. There are no
historical data and scant quantitative data on current populations.
Several populations are now extirpated. Two, and possibly three, of the
subspecies may be extinct (T. m. louiei, T. m. tacomensis, and T. m.
tumuli).
Threats include destruction and alteration of prairie habitat due
to
[[Page 24874]]
development, altered fire regimes, and encroachment of native and
nonnative plants; conflicts with military activities and airport
development and maintenance activities; house cat predation;
consideration as agricultural pests; and vulnerability to naturally
occurring, random events. The magnitude of threats is high due to
patchy and isolated population distributions in habitats highly
desirable for development and subject to a wide variety of human
activities that permanently alter the habitat. There are high and
constant invasions of plant species altering the quality of remaining
habitat. Loss of any of the subspecies will reduce the genetic
diversity and likelihood of the continued existence of the species in
Washington. Threats are imminent because many of those listed above are
ongoing. It is likely that the extirpation of some populations and the
extinction of two, and possibly three, subspecies are the result of one
or more of these threats affecting each of these populations and
subspecies. One subspecies is threatened by gravel pits, and two
subspecies are located on airports with planned development. Because of
the increased imminence of threats, we changed the listing priority
number for each of the eight subspecies of the Mazama pocket gopher
from a 6 to a 3.
Palm Springs (Coachella Valley) round-tailed ground squirrel
(Spermophilus tereticaudus chlorus)--The Palm Springs round-tailed
ground squirrel is one of four recognized subspecies of round-tailed
ground squirrels. The range for the Palm Springs round-tailed ground
squirrel corresponds to the Coachella Valley region in Riverside
County, California. Primary habitat for the Palm Springs round-tailed
ground squirrel in the Coachella Valley is the mesquite sand dune/
hummock community. The species also is found in smaller numbers in
creosote communities on sand dunes and hummocks. Approximately 90
percent of the mesquite hummock communities in the Coachella Valley are
estimated to have been lost since 1939, a reduction from 3,363 hectares
(8,309 acres) to 352 hectares (870 acres). Future development threatens
more mesquite communities occupied by the Palm Springs round-tailed
ground squirrel. The largest unprotected mesquite community in Indio
Hills was recently developed, effectively eliminating a large ground
squirrel population. The rapid growth of urban development in the
Coachella Valley is threatening existing ground squirrel populations
with habitat fragmentation.
A recent taxonomic study that examined the morphology of this
subspecies as well as those of adjacent populations of another
subspecies (S. t. tereticaudus) revealed that the original
classification of this subspecies may be in question. Pelage (hair)
color was found to be different among the two subspecies. In addition,
this study also discovered that putative S. t. tereticaudus populations
in Death Valley, the western central region of the Mojave Desert, and
Borrego Valley were more similar in pelage color to S. t. chlorus in
the Coachella Valley than other S. t. tereticaudus populations from the
Colorado River region of eastern Imperial and Riverside Counties. We
are awaiting peer review of this report before we take action to
reconsider whether this subspecies is valid. In the meantime, we are
seeking funding to pursue a genetic study that will determine this
species' taxonomy based on DNA. Based on our evaluation that the
threats pose an imminent risk of a high magnitude, we changed the
listing priority number for this subspecies from a 6 to a 3.
Washington ground squirrel (Spermophilus washingtoni)--This species
is one of the smallest members of the subgenus Spermophilus, and is
found within the shrub-steppe habitat of the Columbia Basin ecosystem
of Washington and Oregon. The soil types used by the squirrels are
distributed sporadically within the species' range, and have been
seriously fragmented by human development in the Columbia Basin,
particularly by conversion to agricultural use. Where agriculture
occurs, little evidence of ground squirrel use has been documented, and
reports indicate that ongoing agricultural conversion eliminates
Washington ground squirrel habitat. The most contiguous, least-
disturbed expanse of suitable Washington ground squirrel habitat, and
likely the densest distribution of colonies within the range of the
species, occurs on the Boeing site and Boardman Bombing Range in
Oregon, and on Federal and State-owned land in Washington. However, in
Washington, recent declines in some colonies have been precipitous and
the reasons for them are unknown. In 2001, for instance, entire
colonies of ground squirrels were no longer occupied on the Columbia
National Wildlife Refuge and Seep Lakes Management Area near Othello,
Washington, despite the State protected status of the species in the
area. Current and potential threats to the continuing survival of the
species include the following: habitat loss from the conversion of
potential and known habitat to agricultural use, predation,
recreational shooting, disease, potential effects of pesticides, and
potential effects of drought on forage quality and quantity. However,
while the magnitude of threats remains high for the Washington ground
squirrel, the immediacy of threats has declined in the past year. The
majority of existing colonies (in Oregon and throughout the species'
current range) are located on the Boardman Bombing Range and the Boeing
tract, which contain the largest contiguous suitable Washington ground
squirrel habitat. Although Boardman Bombing Range activities are not
certain, they are not expected to change significantly in the
foreseeable future.
In 2003, the largest threat to colonies in Oregon was the imminent
conversion of the Boeing tract for agriculture. This would have
resulted in the permanent loss of habitat for one of the largest
contiguous blocks of Washington ground squirrels. However, in 2004, a
25-year Multi-Species Candidate Conservation Agreement with Assurances
(CCAA) was signed by Threemile Canyon Farms, The Nature Conservancy,
Portland General Electric, Oregon Department of Fish and Wildlife, and
the Service. The parties will implement habitat management, operational
modifications, and conservation measures for four non-listed species,
including the Washington ground squirrel, on approximately 93,000 ac
(37,636 ha) enrolled in the CCAA. Under this agreement, Threemile
Canyon Farms placed 22,600 ac (9,146 ha) of the Boeing tract into a
permanent Oregon Department of Fish and Wildlife Conservation Easement
(Boardman Conservation Area). Also, Portland General Electric
identified 888 ac (356 ha) for management as part of the Conservation
Area for the duration of the CCAA. The Boardman Conservation Area will
be managed by TNC with the goal to maintain and improve where feasible
the integrity of existing native communities and associated species
covered by the CCAA, including the Washington ground squirrel. All but
two known sites and the majority of suitable habitat on the Boeing
tract are located on the Boardman Conservation Area and therefore are
protected from irreversible habitat modification. Based on our current
evaluation of threats, we changed the listing priority number from 2 to
5 for this species as the threats are no longer imminent.
Birds
Spotless crake (Porzana tabuensis), American Samoa Distinct
Population Segment (DPS)--The genus Porzana is widespread in the
Pacific, where it is
[[Page 24875]]
represented by numerous island-endemic and flightless species (many of
which are extinct as a result of anthropogenic disturbances) as well as
several common and cosmopolitan species such as the common crake. The
spotless crake is found in the Philippines, Australia, Fiji, Tonga,
Society Islands, Marquesas, Independent Samoa, and American Samoa. No
subspecies are currently recognized.
The status of populations in other areas is not well known, but the
species is thought to be in decline throughout the oceanic Pacific,
with at least one known extirpation (from the island of Futuna). In
American Samoa, the population of the spotless crake is restricted to
the summit of Tau Island.
The only known population in American Samoa co-occurs with Norway
rats (Rattus norvegicus), which are known to prey on birds and their
eggs and young. The spotless crake is particularly vulnerable because
it is small, nests on the ground, and on Tau summit has no wetland
refuge from predators. Finally, this single population, which existing
survey data suggest is a small population, is at risk from stochastic
occurrences such as typhoons and inbreeding depression. These threats
affect the entire known population of this species in American Samoa,
and are potentially lethal to individuals. The magnitude of threats
facing the species is thus high, and these threats are more imminent
than previously inferred because additional surveys indicate that this
species occurs only as a single, small population in American Samoa.
Although this species may use a wide variety of habitats, wetland
habitats may be necessary for self-sustaining populations of the crake
to persist in the presence of predators. Wetland habitats are limited
in American Samoa, and enforcement of their conservation under local
and Federal law is not consistent. The listing priority number for the
spotless crake is changed from 6 to 3 because surveys on Tau over the
past several years have failed to yield evidence of this species in
locations other than the summit, no observations of this species have
been made during extensive, ongoing surveys of birds elsewhere in
American Samoa, and the threat from rat predation is ongoing.
Friendly ground-dove (Gallicolumba stairi stairi)--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. All six species have some level of threatened status
on the International Union for Conservation of Nature and Natural
Resources (IUCN) Red List. 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
morphological differences between the two are minimal. In American
Samoa, the friendly ground-dove has been found on the islands of Ofu
and Olosega (Manua Group).
Of the primary threats to the subspecies (predation by nonnative
species, poaching and habitat loss), only 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
increases in the population. Predation by introduced species has played
a significant role in reducing and limiting 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). Consistent monitoring using a variety of
methods over the last 5 years yielded few observations 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 ground-dove is limited to steep, rocky slopes; areas that
are not common in American Samoa. Threats to this subspecies have not
changed over the past year, but to better reflect the fact that threats
due to small population size and nonnative predators are imminent, we
revised the listing priority number from a 6 to a 3.
Kauai creeper (Oreomystis bairdi)--The Kauai creeper, or akikiki,
is a small Hawaiian honeycreeper found only on the island of Kauai,
Hawaii, with no described subspecies. The species is known to be
presently facing the primary threats of disease (avian malaria) and
habitat degradation and loss. These threats have persisted over several
decades, and are affecting a large proportion of the population.
The mosquito vector of avian malaria has been found throughout the
range of elevations over which the creeper occurs, and malaria
transmission occurs at least periodically over the species' entire
range. The area of forest where malaria is endemic is likely to
increase with global climate change.
Efforts are underway to reduce habitat loss through control of
invasive nonnative plants in some areas, but there is no weed control
in most of the range of the Kauai creeper, and habitat loss is already
occurring. Also, there are currently no efforts to control habitat
damage by feral ungulates within the range of the Kauai creeper.
A large scale survey in 2000 showed that in the last 30 years the
estimated population declined nearly 80 percent (from 6,832 966 to 1,472 680 birds), the range decreased
approximately 60 percent (from 21,750 to 8,896 acres (8,800 to 3,600
hectares)), and the species has disappeared from much of the periphery
of its range. The listing priority number for the Kauai creeper is
changed from a 5 to a 2 because the threats facing the species are of a
high magnitude and are imminent.
Yellow-billed cuckoo, Western Continental U.S. DPS (Coccyzus
americanus)--While the cuckoo is still relatively common east of the
crest of the Rocky Mountains, biologists estimate that more than 90
percent of the bird's riparian (streamside) habitat in the West has
been lost or degraded. These modifications, and the resulting decline
in the distribution and abundance of yellow-billed cuckoos throughout
the western states, are believed to be due to conversion to
agriculture; grazing; competition from nonnative plants, such as
tamarisk; river management, including altered flow and sediment regime;
and flood control practices, such as channelization and bank
protection. Riparian habitat is continuing to be destroyed through land
use conversion and grazing. Threats to the yellow-billed cuckoo have
not changed over the past year, but to better reflect the fact that
threats are imminent, we revised the listing priority number from a 6
to a 3 for this DPS.
Many-colored fruit-dove (Ptilinopus perousii perousii)--Two
subspecies of the many-colored fruit-dove exist. One, P. p. perousii,
is found in American Samoa, within the four main islands of Tutuila,
Olosega, Ofu, and Tau, and Independent Samoa. Another subspecies, P. p.
mariae, is found in Fiji and Tonga.
The primary threats to P. p. perousii, loss of the native banyan
trees on which it depends, poaching, and predation by nonnative
mammals, are thought to occur at levels insufficient to have a
detrimental effect on the species' population in American Samoa. This
is demonstrated by the fact that 5 years of extensive and intensive
monitoring indicate an increase in the detected
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relative abundance of many-colored fruit-doves in American Samoa. This
trend may have been interrupted by Typhoon Heta in January of 2004,
when damage to their primary food plants, the two species of native
banyan trees, may have altered the doves' foraging to make them more
vulnerable to the opportunistic poaching that typically takes place
after typhoons (Craig et al. 1994).
At present, no disturbance other than typhoons is known to affect
the abundance, distribution, or productivity of native banyans in
American Samoa. Loss of native rainforest harboring these banyans and,
presumably, the nesting habitat for the many-colored fruit-dove is not
currently considered to be taking place at a rate that poses a severe
or imminent risk to the many-colored fruit-dove, and poaching of this
species is thought to be an extremely rare occurrence.
Predation by introduced species has played a significant role in
limiting and extirpating populations of island birds in the Pacific and
other locations worldwide (Atkinson 1977, 1985; Moors and Atkinson
1984). Nonnative predators known to occur in the range of the many-
colored fruit-dove in American Samoa that could be a significant threat
to this arboreal-nesting bird are black rats (R. rattus), Norway rats
(R. norvegicus), and feral cats (Felis catus). However the continued
existence of this species and the recently documented increase in its
abundance, suggest that predation, while a potential threat, is not of
a high-magnitude. The total population size of the many-colored fruit-
dove is unknown, but may number up to a few hundred pairs.
In Independent Samoa, the many-colored fruit-dove may be more
abundant than it is in American Samoa, but this difference likely
reflects difference in island size--the main islands of Independent
Samoa are both an order of magnitude larger than the islands of
American Samoa--and the greater abundance in Independent Samoa of the
two native figs, Ficus prolixa and F. obliqua, that are the preferred
food of this fruit-dove. However, ongoing deforestation (potentially
exacerbated by severe storms) and hunting are considered to threaten
the many-colored fruit-dove in Independent Samoa, and this subspecies'
status there is described as ``Conservation Concern.'' We changed the
listing priority number for the many-colored fruit-dove from 6 to 12
because the overall magnitude of threats is moderate to low and these
threats are not imminent.
Xantus's murrelet (Synthliboramphus hypoleucus)--Xantus's murrelet
is a small seabird of the Alcid family that occurs along the western
coast of North America in the United States and Mexico. Xantus's
murrelet populations in the United States and Mexico appear to have
declined due to a wide variety of threats, with substantial declines
evident at the largest known breeding population and extirpations on
three of the Mexican islands. Data from the largest breeding population
on Santa Barbara Island in the United States indicated a dramatic
decline (as much as 70 percent from 1977 to the mid-1990s); data from
other islands are scarce.
Although the decline in Xantus's murrelet populations appears to
have been substantial, some of the largest threats are being addressed,
and, to some degree, ameliorated in the United States. For example,
although predation is a large contributor to the current low population
numbers of the Xantus's murrelet, it does not pose as imminent a threat
as it once did. Cats and rats have been removed from many of the
islands where they once occurred. Anacapa Island implemented a rat
eradication program in 2001 that seems to have been successful in
removing that nonnative predator of the Xantus's murrelet. Rats were
eradicated in 1994 from San Roque Island. Although the nonnative
herbivores have been absent from Santa Barbara Island since the late
1950s, their presence facilitated the introduction of non-native
grasses, which continue to exist and spread on that island. The
conversion of native habitat to nonnative grassland that has occurred
on Santa Barbara Island poses a threat to the population of Xantus's
murrelet due to the fact that the island is only one square mile in
size and holds the majority of the nesting population in California.
Introduction of nonnative grasses has modified the habitat. Such
habitat modification is thought to have increased the endemic deer
mouse (Peromyscus maniculatus elusus) population, a native predator of
Xantus's murrelet eggs.
The Service has been working with the State of California, National
Park Service, and National Marine Fisheries Service to address the
threats of light pollution and human disturbance. Many nocturnal birds
are attracted to the lights of commercial fishing vessels and Xantus's
murrelets and other seabirds become exhausted from continual attraction
and fluttering near lights or collide with lighted vessels, the impact
resulting in injury or death. Chicks have been documented to separate
from their parents due to vessel lights, often resulting in death as
chicks are dependent on parents for survival. Additionally, squid boats
operate in shallow waters close to Xantus's murrelet breeding colonies
in the California Channel Islands. Increased predation on Xantus's
murrelets by Western gulls (Larus occidentalis) and barn owls (Tyto
alba) as a result of lighting, particularly from squid boats, near
breeding colonies has been documented. To address the threat from light
pollution, the California Department of Fish and Game implemented
regulations to require shielding and limit wattage of lights used by
boats conducting nighttime fishing activities. Although these
regulations do not remove the negative effects of this activity, they
likely have resulted in a reduction of the impacts. Although not likely
responsible for the species' current low numbers, oil pollution may
pose a potential threat to the survival of the Xantus's murrelet
population.
Despite actions to address some of the threats to this species, a
recent proposal by ChevronTexaco Corporation to build a liquid natural
gas (LNG) facility 600 meters offshore Islas Los Coronados in Baja
California, Mexico, poses a threat to the survival of the Xantus's
murrelet. The Los Coronados islands support the largest known breeding
population of Xantus's murrelets in the world. The construction and
operation of the proposed LNG facility at Islas Los Coronados would
increase levels of disturbance to Xantus's murrelets. Sources of
disturbance include: (1) Bright lights at night from the facility and
visiting tanker vessels; (2) noise from the facility; (3) noise from
helicopters visiting the facility; (4) ingress and egress of tanker
vessels; and (5) other vessels transporting personnel and supplies.
These factors would have a serious impact on the islands' population of
Xantus's murrelets, and, taken together, the cumulative disturbance
caused by this proposed facility would have substantial negative
consequences for the colony.
Additionally, there are potential impacts to the Xantus's murrelet
prey base due to increased seawater chlorination resulting from this
facility. The ocean waters around Islas Los Coronados are highly
productive and very important foraging areas for breeding, migrant, and
wintering seabirds such as the Xantus's murrelet. The loss of large
numbers of prey could be detrimental to seabirds that depend on Islas
Los Coronados for foraging at various times of year. Degraded water
quality around Islas Los Coronados may also result from this project,
such as
[[Page 24877]]
from the seawater chlorination process. A gas spill from the facility
or pipeline could have substantial negative effects on the Xantus's
murrelet. Due to the now imminent threats from the proposed LNG
facility, we changed the listing priority number for this species from
a 5 to a 2.
Amphibians
Black Warrior waterdog (Necturus alabamensis)--The Black Warrior
waterdog 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, however, as limited attention was given to this
species between its description in 1937 and the 1980's. There are a
total of 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 1990's 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. An
additional threat to the Black Warrior waterdog is the creation of
large impoundments that have flooded thousands of acres of its habitat.
These impoundments are likely marginal or unsuitable habitat for the
salamander. Threats to the Black Warrior waterdog have not changed over
the past year, but to better reflect the fact that threats from the
pervasive water quality degradation in the Black Warrior Basin are
imminent, we changed the listing priority number from a 5 to a 2 for
this species.
Ozark hellbender (Cryptobranchus alleganiensis bishopi)--Since the
species was elevated to candidate status in 2001 (66 FR 54808), the
known threats have increased. In particular, recreational pressures on
Ozark hellbender rivers have increased substantially on an annual
basis. The Missouri Department of Conservation reports that gigging
popularity and pressure has increased, which presents a significant
threat to hellbenders during the breeding season as they tend to move
greater distances and congregate in small groups where they are an easy
target for giggers. Canoe, kayak, and motor/jet boat traffic has
increased in recent years on the Jacks Fork, Current, Eleven Point, and
North Fork Rivers. The popularity of these float streams has grown to
the point that the National Park Service is considering alternatives to
reducing the number of boats that can be launched daily by
concessionaires, but no change has been adopted and even if one is,
floating will still occur. Horse trail rides are extremely popular
along both the Jacks Fork and Current National Scenic Rivers. In 2003,
the Missouri Department of Natural Resources added a 7-mile stretch of
the Jacks Fork River to the 303(d) list of impaired waters for organic
wastes (fecal coliform) immediately downstream from a commercial horse
trail ride outfitter.
To date, nothing has been done to reduce or ameliorate ongoing
threats to Ozark hellbenders. The Ozarks region continues to experience
rapid urbanization, expansion of industrial agricultural practices such
as concentrated animal feeding operations (chickens, turkeys, hogs,
cattle), and logging. No laws are in place that preclude livestock from
grazing in riparian corridors and resting in or along streams and
rivers. Missouri is the second largest beef cattle producing state in
the nation, with the majority of animal units produced in the Ozarks.
Both Arkansas and Missouri are the leading States in poultry
production. The fact that the majority of the Ozarks region in Missouri
and Arkansas is comprised of karst topography (caves, springs,
sinkholes, and losing streams) further complicates the containment and
transport of potential contaminants.
In short, the abundance of treatment facilities and lack of
adequate treatment facilities or practices for both human and livestock
waste poses a significant and ever increasing threat to aquatic
ecosystems. The decrease in Ozark hellbender range and population size
and the shift in age structure are likely caused by a variety of
historic and ongoing activities. The primary cause of these trends is
habitat destruction and modification through impoundment,
channelization, siltation, and water quality degradation from a variety
of sources, including industrialization, agricultural runoff, mine
waste, and timber harvest. Overutilization of hellbenders for commerce
and scientific purposes is also likely contributing to their decline.
The regulations in place that could prevent these impacts, including
the Clean Water Act and State laws, have been inadequate in preventing
Ozark hellbender declines to this point. Finally, most of the remaining
Ozark hellbender populations are small and isolated, making them
vulnerable to individual catastrophic events and reducing the
likelihood of recolonization after localized extinctions. Due to
substantial increases in recreational pressures on Ozark hellbender
rivers on an annual basis, we changed the listing priority number for
this subspecies from a 6 to a 3.
Clams
Georgia pigtoe (Pleurobema hanleyanum)--The Georgia pigtoe was
historically found in shallow runs and riffles in large creeks and
rivers of the Coosa River drainage system in Alabama, Georgia, and
Tennessee. The species is currently known to exist in localized
portions of the upper Conasauga River in Murray and Whitfield Counties,
Georgia, and in a short reach of the Coosa River below Terrapin Creek,
Cherokee County, Alabama. The Georgia pigtoe is very rare, with only a
few observations of living animals over the past 15 years. Impoundment
and pollution are implicated in the decline and disappearance of the
species. We changed the listing priority of the Georgia pigtoe from a 5
to a 2 due to rarity and continued lack of success into locating living
animals.
Snails
Bonneville pondsnail (Stagnicola bonnevillensis)--The Bonneville
pondsnail occupies four spring pools north of the Great Salt Lake in
Box Elder County, Utah (Horse Spring B, Horse Spring B South, Pipe
Spring, and Shotgun Spring). While the total number of individuals is
unknown, the total occupied habitat is less than one hectare. Two
previous threats to this species now appear to have been resolved.
Leaks from petroleum pipelines in the area have occurred in 2000 and
2002; however, Chevron Pipeline (which has responsibility for operation
and maintenance of the pipelines) has addressed potential threats from
pipeline leaks with internal integrity inspections and alerts prior to
leakage. Consequently, potential pipeline leaks are not a current
threat. Intensive, unregulated grazing can degrade the habitat of
aquatic species, including Stagnicola bonnevillensis, but the springs
where this species occurs
[[Page 24878]]
have been fenced to restrict livestock use and this is not a current
threat.
Current threats to this species include perchlorate and
trichloroethelene (TCE) contamination from ATK Thiokol, Inc. (Thiokol).
Until recently, Thiokol disposed of waste products such as perchlorate
and TCE in an area 6.5 km (4 mi) upstream from the pondsnail's habitat,
within the same hydrologic ground water gradient as the occupied snail
habitat. Contaminated soils have been removed and the area capped to
prevent further contamination. Groundwater sampling indicates that the
10 [mu]g/l isoline of the TCE plume is 0.5 km (0.3 mi) north of Shotgun
and Pipe Springs. The 100 [mu]g/l isoline of the TCE plume is 2.4 km
(1.5 mi) northwest of Shotgun Spring. The 1000 [mu]g/l isoline of the
TCE plume is 3.5 km (2.2 miles) northwest of Shotgun Spring. Levels of
percholate measured in June 2004 range from 6.6 [mu]g/liter in Fish
Spring to 287 [mu]g/liter in Pipe Spring. The acute toxicity of TCE and
perchlorate to Stagnicola bonnevillensis is under investigation, but
both substances are potentially lethal to most wildlife species. The
current levels of TCE and perchlorate in the occupied springs and the
approaching groundwater plume are of concern for the future of this
species and its habitat. Thiokol is taking corrective action to
identify and remediate groundwater contamination through a Corrective
Action Plan (an updated groundwater model and risk assessments are to
be completed in May 2005 under this plan). Bioassay studies are being
initiated to determine the effect of these contaminants on the snail
and its habitat.
Although the range of this species is highly restricted and the
only known habitat is currently threatened by chemical contamination of
the ground water, we consider the following actions that are addressing
these threats to be significant enough to have reduced the magnitude of
threats from high to moderate: discontinued disposal of wastes in an
unlined impoundment, removal of contaminated soil, installation of a
cap to prevent infiltration of water into soils beneath impoundment,
monitoring of downgradient groundwater for contamination,
implementation of a Corrective Action Plan to characterize and
remediate groundwater contamination, implementation of a site
management plan, and development of a groundwater model and risk
assessment. Thus, we changed the listing priority from a 2 to an 8.
Additionally, the Utah Division of Wildlife Resources is currently
drafting a Conservation Agreement and Strategy for this species.
Interrupted (Georgia) rocksnail (Leptoxis foremani (downei))--
Interrupted rocksnails historically occurred in shoals, riffles, and
reefs of small to large rivers in the Coosa River Basin of Alabama and
Georgia. Today, only a single surviving natural population is known
from a short reach of the Coosawattee River, Georgia. During a 1999
census, 10-45 interrupted rocksnail snails per square meter were found
in this reach. In 2004, a 6 man-hour search was required to find 20
individuals. Water quality is suspected as the cause of decline. A
captive colony of approximately 200 snails was established at the
Tennessee Aquarium Research Institute (TNARI) in 2000 for study and
propagation. During the winter of 2003, the Alabama Department of
Conservation and Natural Resources released about 3000 juvenile
interrupted rocksnails from the TNARI colony into the Coosa River above
Wetumpka, Elmore County, Alabama. The status of this reintroduction is
currently unknown. We changed the listing priority number for the
interrupted rocksnail from a 5