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, 53756-53835 [06-7375]
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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.
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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 landowners and
resource managers to alleviate threats
and thereby possibly remove the need to
list species as endangered or threatened.
Even if we subsequently list a candidate
species, the early notice provided here
could result in more options for species
management and recovery by prompting
candidate conservation measures to
alleviate threats to the species.
The CNOR summarizes the status and
threats that we evaluated in order to
determine that species qualify as
candidates and to assign a listing
priority number to each species, or to
remove species from candidate status.
Additional material that we relied on is
available in the Species Assessment and
Listing Priority Assignment Forms
(species assessment forms, previously
called candidate forms) for each
candidate species.
Overall, this CNOR recognizes 7 new
candidates, changes the listing priority
number for 24 candidates, and removes
10 species from candidate status.
Combined with other decisions for
individual species that were published
separately from this CNOR, the new
number of species that are candidates
for listing is 279.
We request additional status
information that may be available for
the 279 candidate species identified in
this CNOR. We will consider this
information in preparing listing
documents and future revisions to the
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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 consider including as
candidates as we prepare future updates
of this notice.
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 2, 2005, through August 23, 2006.
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. As defined in section 3 of
the Act, an endangered species is any
species which is in danger of extinction
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throughout all or a significant portion of
its range, and a threatened species is
any species which is likely to become
an endangered species within the
foreseeable future throughout all or a
significant portion of its range. Through
the Federal rulemaking process, we add
species that meet these definitions to
the List of Endangered and Threatened
Wildlife at 50 CFR 17.11 or the List of
Endangered and Threatened Plants at 50
CFR 17.12. As part of this program, we
maintain a list of species that we regard
as candidates for listing. A candidate
species is one for which we have on file
sufficient information on biological
vulnerability and threats to support a
proposal to list as endangered or
threatened, but for which preparation
and publication of a proposal is
precluded by higher-priority listing
actions.
We maintain this list of candidates for
a variety of reasons: To notify the public
that these species are facing threats to
their survival; to provide advance
knowledge of potential listings that
could affect decisions of environmental
planners and developers; to provide
information that may stimulate and
guide conservation efforts that will
remove or reduce threats to these
species and possibly make listing
unnecessary; to 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.
We strongly encourage collaborative
conservation efforts for candidate
species and offer technical and financial
assistance to facilitate such efforts. For
additional information regarding such
assistance, please contact the
appropriate Regional Office listed in
SUPPLEMENTARY INFORMATION or visit our
Internet Web site, https://
endangered.fws.gov/candidates/
index.html.
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 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, referring to them as species
considered to be candidate endangered
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or threatened species. We published a
new comprehensive notice of review for
native plants on December 15, 1980 (45
FR 82479), which took into account the
earlier Smithsonian report and other
accumulated information. On November
28, 1983 (48 FR 53640), our
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); May 4, 2004 (69
FR 24876); and May 11, 2005 (70 FR
24870). 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 (i.e. vertebrate and
invertebrate) animal notice of review on
January 6, 1989 (54 FR 554), with minor
corrections on August 10, 1989 (54 FR
32833). We again published
comprehensive animal notices on
November 21, 1991 (56 FR 58804) and
November 15, 1994 (59 FR 58982).
Beginning in 1996 we published
combined animal and plant notices,
including those published 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);
May 4, 2004 (69 FR 24876); and May 11,
2005 (70 FR 24870). 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.
On September 21, 1983, we published
guidance for assigning a listing priority
number (LPN) for each candidate
species (48 FR 43098). We continue to
use this guidance to assign each
candidate a LPN of 1 to 12, depending
on the magnitude of threats, imminence
of threats, and taxonomic status. Such a
priority ranking guidance system is
required under section 4(h)(3) of the Act
(15 U.S.C. 1533(h)(3)).
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This revised notice supersedes all
previous animal, plant, and combined
notices of review.
Summary of This CNOR
Since publication of the 2004 CNOR
on May 11, 2005 (70 FR 24870), 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 number assigned to each
species. We also evaluated the need to
emergency-list any of these species,
particularly species with high priorities
(i.e. species with listing priority
numbers of 1, 2, or 3). This review and
reevaluation ensures that we focus
conservation efforts on those species at
greatest risk. In addition to reviewing
candidate species, the Service has
worked on numerous findings in
response to petitions to list species and
has prepared proposed and final
determinations for rules to list species
under the Act; some of these findings
and determinations have been
completed and published in the Federal
Register while work on others is still
underway (see Preclusion and
Expeditious Progress, below, for
details). Since publication of the CNOR
last year the Service has completed and
published final rules listing 2 species as
endangered and 17 species as
threatened; reviewed the status of and
published findings that listing proposals
are not warranted for 4 species; and
published proposed rules for listing for
3 species for which final determinations
are pending.
Based on our review of the best
available scientific and commercial
information, this CNOR identifies 7 new
candidate species (see New Candidates,
below), changes the listing priority
number for 24 candidates (see Listing
Priority Changes in Candidates, below)
and determined that listing proposals
are not warranted for an additional 10
species and thus have removed them
from candidate status (see Candidate
Removals, below). Combined with the
other decisions published separately
from this CNOR for individual species
that previously were candidates, a total
of 279 species, including 140 plant and
139 animal species, are now candidates
awaiting preparation of rules proposing
their listing. These 279 species, along
with the 3 species currently proposed
for listing, are included in Table 1.
Table 2 includes 33 species identified
in the previous CNOR as either
proposed for listing or classified as
candidates that are no longer in those
categories. This includes the 19 species
we listed as threatened or endangered
since the previous CNOR and the 4
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species for which we published separate
findings that listing is not warranted,
plus the 10 species that we have
determined do not warrant preparation
of a rule to propose listing and therefore
have removed from candidate status in
this CNOR.
New Candidates
Below we present brief summaries of
seven new candidates that we are
recognizing in this CNOR, including one
species of mammal, one bird, two snails,
two insects, and one plant. 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). For each of these seven
species, we find that we have on file
sufficient information on biological
vulnerability and threats to support a
proposal to list as endangered or
threatened, but that preparation and
publication of a proposal is precluded
by higher-priority listing actions (i.e.
these meet our definition of a candidate
species). Two of these seven species
were petitioned for listing, and for those
two species this constitutes our finding,
as required pursuant to section
4(b)(3)(B)(iii) of the Act, 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, and that expeditious progress is
being made to add qualified species to
the lists of threatened and endangered
species and to remove from such lists
species for which the protections of the
Act are no longer necessary. (Additional
information is provided in the sections
entitled Petition Findings and
Preclusion and Expeditious Progress,
below). We also note below that one
other species, a fish, was identified as
a candidate earlier this year in a
separate finding published in the
Federal Register.
Mammals
New England cottontail (Sylvilagus
transitionalis)—The following summary
is based on information from our files
and information collected during the
public comment period on our 90-day
petition finding. On August 30, 2000,
we received a petition to list this
species. We published our 90-day
finding on June 30, 2004 (69 FR 39395).
The New England cottontail (NEC) is
a medium- to large-sized cottontail
rabbit that may reach 1,000 grams in
weight, and is one of two species within
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the genus Sylvilagus occurring in New
England. New England cottontails are
considered habitat specialists, in so far
as they are dependent upon earlysuccessional habitats typically
described as thickets. The species is the
only endemic cottontail in New
England.
Historically, the NEC ranged from
southeastern New York (east of the
Hudson River) north through the
Champlain Valley, southern Vermont,
the southern half of New Hampshire,
southern Maine, and south throughout
Massachusetts, Connecticut, and Rhode
Island. The species is now considered to
be extirpated from Vermont, the current
range elsewhere has declined
substantially, and occurrences have
become increasingly separated. The
species’ current distribution is
fragmented into five apparently isolated
metapopulations in about 14 percent of
the species’ historical range. The range
has contracted from approximately
90,000 sq km to 12,180 sq km, and
much of the suitable habitat within the
current range is in small patches that are
not occupied by the NEC. A multi-state,
regional inventory conducted in 2001–
2004 found New England cottontails
were absent from 93% of approximately
2,300 habitat patches within the recent
historical range (1990 to present) that
were searched for the presence of the
species. Many of the occupied sites
were quite small (3 acres or less) and are
considered by some researchers to be
population ‘‘sinks.’’ It is estimated that
less than one-third of the occupied sites
occur on lands in conservation status,
and fewer than 10 percent of these sites
in conservation status are being
managed for early successional forest
species such as the NEC.
The primary threat to the New
England cottontail is ongoing
destruction and modification of its
remaining habitat through natural
succession processes and through
alteration related to human
development and other activities.
Isolation of occupied patches of habitat
by areas of unsuitable habitat, as well as
predation, appears to be resulting in
local extirpation of New England
cottontails from small patches. Based on
current land uses in the region, the loss
of about 2 percent of its current range
per year is expected to continue.
Additional threats include competition
for food and habitat with introduced
eastern cottontails and large numbers of
native white-tailed deer, and inadequate
regulatory mechanisms in effect to
protect the habitat. Based on threats of
high magnitude that are imminent, we
assigned this species a listing priority
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number of 2. (See also the section
entitled Petition Findings, below)
Birds
Red knot (Calidris canutus rufa)—The
following summary is based on
information from our files and
information provided by petitioners. We
received one petition on August 9, 2004,
and two others were each received on
August 5, 2005.
The rufa subspecies is one of six
recognized subspecies of red knot and
one of three subspecies occurring in
North America (hereafter all mention of
red knot refers strictly to the rufa
subspecies). This subspecies makes one
of the longest distance migrations
known in the animal kingdom as it
travels between breeding areas in the
central Canadian Arctic and wintering
areas that are primarily in southern
South America along the coast of Chile
and Argentina. They migrate along the
Atlantic coast of the United States
(U.S.), where they may be found from
Maine to Florida. The Delaware Bay
area (in Delaware and New Jersey) is the
largest known spring migration stopover
area, with far fewer migrants
congregating elsewhere along the
Atlantic coast. The concentration in the
Delaware Bay area occurs from the
middle of May to early June,
corresponding to the spawning season
of horseshoe crabs. The knots feed on
horseshoe crab eggs, rebuilding energy
reserves needed to complete migration
to the Arctic and arrive on the breeding
grounds in good condition.
Surveys at wintering areas and at
Delaware Bay during spring migration
indicate a substantial decline in recent
years. At the Delaware Bay area, peak
counts between 1982 and 1998 were as
high as 95,360 knots. Although counts
may vary considerably between years,
some of the population fluctuations can
be attributed to predator-prey cycles in
the breeding grounds, and counts show
that knots rebound from such
reductions. In the past, horseshoe crab
eggs were so numerous that a knot could
eat enough in two to three weeks to
double its weight. Research shows that
from 1997 to 2002 an increasing
proportion of red knots leaving the
Delaware Bay failed to achieve
threshold departure masses needed to
fly to breeding grounds and survive an
initial few days of snow cover, and this
corresponded to reduced annual
survival rates. Recently, peak counts at
the Delaware Bay area have been lower
than in the past and do not show a
rebound. The peaks were 13,315 in
2004, 15,345 in 2005, and 13,455 in
2006. Counts in recent years at the
principal wintering areas in South
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America also are substantially lower
than in the past and do not show a
rebound.
The primary factor threatening the red
knot is destruction and modification of
its habitat, particularly the reduction in
key food resources resulting from
reductions in horseshoe crabs, which
are harvested primarily for use as bait
and secondarily to support a biomedical
industry. Commercial harvest increased
substantially in the 1990’s. Since 1999,
a series of timing restrictions and
substantially lower harvest quotas have
been adopted by the Atlantic States
Marine Fisheries Commission (ASMFC),
as well as New Jersey and Delaware. In
May 2006, the ASMFC adopted
restrictions effective from October 1,
2006 to September 30, 2008, including
a prohibition on harvest and landing of
horseshoe crabs in New Jersey and
Delaware from January 1 through June 7,
harvest of males only from June 8
through December 31, and harvest
limited to no more than 100,000
horseshoe crabs per state per year. The
ASMFC also adopted other restrictions
applicable to Maryland and Virginia.
New Jersey has established restrictions
which supersede those of the ASMFC;
as a result there is a moratorium on all
horseshoe crab harvest in New Jersey
from May 15, 2006 through June 7,
2008, after which the restrictions
adopted by ASMFC apply.
The reductions in commercial harvest
since 1999 are substantial: 726,660
horseshoe crab landings for bait were
reported in 1999 in Delaware and New
Jersey, compared to 173,777 in 2004.
However, we do not know whether
horseshoe crab populations will rebuild
or how long a lag time there may be in
increased availability of eggs, as they
need 8–10 years to reach sexual
maturity and other key information for
estimating population response is
lacking. A survey in Delaware Bay
showed spawning activity was stable or
slightly declining from 1999 to 2004. In
2004, availability of horseshoe crab eggs
on principal shorebird foraging beaches
increased over recent years. The peak
number of migrant red knots observed at
Delaware Bay increased slightly in 2005
compared to 2004, and in 2006 the peak
count was similar to that in 2004. Also,
body weights of red knots at the time of
departure from Delaware Bay improved
in 2005 over previous years. Counts of
red knots at key wintering areas in
South America, although much reduced
from the past, were similar in 2006 to
the counts in 2005. Thus in recent years
the number of knots has been much
lower than in the past and the trend in
the abundance is not improving despite
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a four-fold reduction in horseshoe crab
landings since the late 1990’s.
Other identified threat factors include
habitat destruction due to beach erosion
and various shoreline protection and
stabilization projects that are impacting
areas used by migrating knots for
foraging, the inadequacy of existing
regulatory mechanisms, human
disturbance, and competition with other
species for limited food resources. Also,
the concentration of red knots in the
Delaware Bay area and at a relatively
small number of wintering areas make
the species vulnerable to potential largescale events in those areas such as large
oil spills or severe weather.
Overall, we conclude that the threats,
in particular the modification of habitat
through harvesting of horseshoe crabs to
such an extent that it puts the viability
of the knot at substantial risk, are of a
high magnitude, but are nonimminent
because of reductions and restrictions
on harvesting horseshoe crabs.
Accordingly, we assigned a listing
priority number of 6 to this subspecies.
(See also the section entitled Petition
Findings, below)
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Fish
Headwater chub (Gila nigra)—We
previously announced candidate status
for this species in a separate warrantedbut-precluded 12-month petition
finding, published on May 3, 2006 (71
FR 26007).
Snails
Black mudalia (Elimia melanoides)—
The following summary is based on
information in our files. The historical
and current range of the black mudalia,
an aquatic snail, is in Alabama. The
historical range included much of the
upper half of the Black Warrior River
drainage, including the main stem Black
Warrior above Tuscaloosa, as well as the
Sipsey Fork and Locust Fork. The black
mudalia is currently known from five
localized shoals in an approximately 30mile reach of the upper Locust Fork of
the Black Warrior River, and from two
shoals in a 1-mile reach of the
Blackburn Fork of the Little Warrior
River, a tributary of the Locust Fork.
The black mudalia requires flowing
water, and the construction of two major
dams on the main stem Black Warrior
River above the Fall Line (Oliver Lock
and Dam, 1940; Holt Dam, 1966) and
another dam on the lower Sipsey Fork
(Bankhead Dam, 1975), impounded
much of the species’ historical habitat.
Dams eliminate or reduce currents
within impounded areas, allowing
sediments to accumulate on inundated
channel habitats. Impounded waters
also experience changes in water
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chemistry that can affect survival or
reproduction of black mudalia.
The primary threats to the black
mudalia in the areas it currently
occupies involve habitat destruction
and modification, particularly in
relation to poor water quality and
habitat deterioration. Point-source
discharges and surface runoff cause
nutrification, decreased dissolved
oxygen concentration, increased acidity
and conductivity, and other changes in
water chemistry which are likely to
seriously affect aquatic snails. Pollution
from surface runoff can originate from a
wide array of land use activities, and
may include sediments, fertilizers,
herbicides, pesticides, animal wastes,
septic tank and gray water leakage, and
oils and greases. Land uses in the
vicinity of black mudalia populations
include pasture, row crops, timber
production, and chicken farms. Because
the threats to black mudalia are of a
high magnitude and are imminent, we
assigned a listing priority of 2 to this
species.
Rough hornsnail (Pleurocera
foremani)—The following summary is
based on information in our files. The
rough hornsnail is an aquatic snail
endemic to the Coosa River system in
Alabama. It currently is known to occur
at two locations: The lower Yellowleaf
Creek in Shelby County, and the lower
Coosa River below Wetumpka Shoals in
Elmore County. Searches of historical
habitats in the Coosa River and its
tributaries have failed to locate the
species at other localities. The two
surviving populations are extremely
small and localized. The historical
habitats of the rough hornsnail have
been extensively modified by six large
dams constructed for hydropower
production. Dams eliminate or reduce
currents within impounded areas,
allowing sediments to accumulate on
inundated channel habitats. Impounded
waters also experience changes in water
chemistry that can affect survival or
reproduction of pleurocerid snails.
Currently, the primary threat to the
rough hornsnail is habitat destruction
and modification related to poor water
quality and habitat deterioration that
result from point source discharges and/
or surface runoff. These actions cause
nutrification, decreased dissolved
oxygen concentration, increased acidity
and conductivity, and other changes in
water chemistry that can seriously affect
aquatic snails. Both populations of the
rough hornsnail are in areas currently
experiencing high human population
growth and development. Because the
threats are ongoing and are of a high
magnitude, we assigned the rough
hornsnail a listing priority of 2.
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Insects
Florida leafwing butterfly (Anaea
troglodyta floridalis)—The Florida
leafwing is endemic to south Florida
and the Keys; it occurs only within pine
rocklands that retain its sole hostplant,
pineland croton (Croton linearis). Once
locally common within the formerly
widespread pine rockland habitat that
occurred within Miami-Dade and
Monroe Counties and less common and
sporadic within Collier, Martin, Palm
Beach, and Broward Counties, the
leafwing now has small and isolated
populations at only two locations: On
Big Pine Key in the lower Florida Keys,
and Long Pine Key on the Florida
mainland. On Big Pine Key, the
butterfly and its habitat occur on
National Key Deer Refuge (NKDR) and
also on other scattered private and
public lands within the vicinity of
NKDR. On the Florida mainland, the
population on Long Pine Key is within
Everglades National Park (ENP). Pine
rockland fragments on the mainland
near or adjacent to ENP may still retain
the potential to support some small,
localized, and sporadic populations of
the butterfly, but no Florida leafwings
have been documented as occurring in
such areas outside ENP for the last
several years.
Land developments of various types
have greatly reduced pinelands in
Florida. Within the Keys, pinelands
containing the pineland croton
hostplant now occur only on Big Pine
Key, with an estimated 80 hectares (ha)
(198 acres) within NKDR and small,
scattered relict sites elsewhere. On the
mainland, an estimated 1,068 ha (2,638
acres) of appropriate hostplant-bearing
habitat occur within ENP on Long Pine
Key; outside that area, in Miami-Dade
County, scattered fragments of pine
rockland containing pineland croton
occur in fragments that collectively total
approximately 370 (ha) (916 acres),
roughly half of which are in private
ownership. Collectively, the Big Pine
Key, Long Pine Key, and relict pine
rocklands adjacent to ENP presently
support an estimated total of 100–800
adult Florida leafwing butterflies at any
given time.
The Florida leafwing is vulnerable to
impacts that probably did not pose
significant risks to its continued
existence in the past, when suitable
habitat and the species were much more
abundant and widespread. Habitat
destruction and modification is a
continuing problem on public and
private lands. This includes habitat loss
due to unnatural or altered fire regimes.
Natural fires are important in
maintaining the herbaceous layer of
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pine rocklands, of which the butterfly’s
sole hostplant, pineland croton, is a
part. Without these fires, succession
from pinelands to hardwood hammocks
is rapid, with loss of suitable habitat for
the Florida leafwing. Due to the
proximity of remaining pine rockland
habitat to urban areas in southern
Florida and the Keys, most natural fires
have been and are suppressed, often
replaced by inconsistent regimes of
managed or prescribed fires that do not
necessarily result in habitat conditions
suitable for the Florida leafwing.
Prescribed burning occurs on portions
of ENP on Long Pine Key, and ENP is
working on incorporating
considerations for life histories of select
butterfly species into their management.
At NKDR, private homes and light
commercial uses are embedded within
or in close proximity to the firesustained pineland habitat. Thus
management of pine rocklands is
particularly difficult due to the mixed
pattern of land ownership and
development. Fire suppression to
protect residential areas results in the
invasion and replacement of native pine
rockland habitat by hardwood
hammocks, thereby causing continued
loss of habitat for the leafwing. Survey
data collected from mid-2003 through
July 2006 indicate a substantial decline
in leafwing numbers on NKDR, even
within an area where prescribed
burning occurs. Outside of NKDR and
ENP, much of the remaining suitable
habitat for the Florida leafwing on
private land is subject to destruction or
modification due to the effects of fire
suppression or due to the nature of
prescribed fire activities, and continued
economic development that results in
conversion of pine rocklands to other
uses.
The continued existence of the
Florida leafwing also is threatened due
to other natural and human-related
factors. Pesticides used in mosquito
control practices are a major threat on
Big Pine Key, where nearly all occupied
and suitable habitat for the Florida
leafwing is exposed to mosquito control
chemicals. Studies have shown that the
pesticides used for mosquito control at
field application rates are extremely
toxic to non-target butterflies, skippers,
and moths. Essentially all of the pine
rocklands within NKDR except one area,
Watson’s Hammock, are sprayed and
residential areas and roadsides across
Big Pine Key are treated. Also, chemical
drift of pesticides has been found 750
meters (2,460 feet) within the borders of
the no-spray zone on Watson’s
Hammock. Mosquito control poses
much less of a risk to the leafwings in
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ENP, as mosquito control on Long Pine
Key is limited to residential areas and
campgrounds. Additional natural and
human-related factors include the risk
of direct mortality and habitat loss due
to extreme weather events (e.g.
hurricanes, tropical storms), and risk of
reduced genetic diversity; both of these
risks are heightened due to the
reduction of the Florida leafwing to
small, isolated populations.
The established interest in specimens
of the leafwing and information requests
regarding its location from collectors,
researchers, and others suggests that
collection may be occurring and has the
potential to occur at any time. However,
we do not have sufficient information to
conclude that overutilization for
commercial, recreational, scientific, or
educational purposes is a factor that
threatens the Florida leafwing. The
principal threats to the Florida leafwing
at this time are the destruction,
modification, or curtailment of its
habitat or range, and other natural or
manmade factors affecting its continued
existence. Based threats of high
magnitude that are imminent, we
assigned a listing priority number of 3
to the Florida eafwing butterfly.
Bartram’s hairstreak butterfly
(Strymon acis bartrami)—The following
summary is based on information in our
files. The Bartram’s hairstreak is a
subspecies endemic to south Florida
and the Keys. Like the Florida leafwing
butterfly (described above) it occurs
only within pine rocklands that retain
its sole hostplant, pineland croton
(Croton linearis). Once locally common
within the formerly widespread pine
rockland habitat that occurred within
Miami-Dade and Monroe Counties, and
less common and sporadic within
Collier, Palm Beach, and Broward
Counties, the Bartram’s hairstreak is
now largely restricted to two locations:
Big Pine Key in the Florida Keys, and
Long Pine Key on the Florida mainland.
On Big Pine Key, the butterfly and its
habitat occur on National Key Deer
Refuge and also on other scattered
private and public lands in the vicinity
of NKDR. On Long Pine Key the species
is within Everglades National Park. Pine
rockland fragments near or adjacent to
ENP also appear to retain some small,
localized, and sporadic populations of
the butterfly. The same factors
identified as threats to the Florida
leafwing butterfly (summarized above)
also threaten Bartram’s hairstreak. Based
on threats of high magnitude that are
imminent, we assigned a listing priority
number of 3 to Bartram’s hairstreak
butterfly.
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Flowering Plants
Harrisia aboriginum (Aboriginal
pricklyapple)—The following summary
is based on information in our files.
This cylindrical-stemmed cactus
currently occurs in coastal strand
vegetation and tropical coastal
hammocks on coastal islands of
Sarasota, Charlotte, and Lee Counties,
Florida, from Longboat Key south to
Buck Key in the J.N. ‘‘Ding’’ Darling
National Wildlife Refuge. Populations
are likely to be on shell mounds or sites
with shelly substrates; plants may be
quite close to the mangrove zone, but
not in it. This plant always had a
restricted distribution and is now
vulnerable to extinction because only 10
populations are remaining. Each
population occurs just above sea level
along the coast, and is threatened by the
rise in sea level that has occurred during
the past century and is continuing. Each
population is also threatened by
nonnative plant invasions and, in at
least one case, predation by introduced
iguanas. Some populations are on
private lands, and these are all
vulnerable to habitat destruction and/or
improper management. Additionally,
the proximity to the coast, combined
with the very small number of plants in
each population, makes the species
vulnerable to hurricanes which have the
potential to overwash islands and
extirpate populations. For these reasons,
the magnitude of threats is high.
Overall, threats are nonimminent
because public land managers have been
and are continuing to address exotic
invasive plant issues. Therefore, we
assigned this species a listing priority
number of 5.
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 one
case, reflects 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.
Birds
Friendly ground-dove, American
Samoa DPS (Gallicolumba stairi stairi)—
The following summary is based on
information contained in our files. The
genus Gallicolumba is distributed
throughout the Pacific and Southeast
Asia. The genus is represented in the
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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). Threats to this subspecies have
not changed over the past year. Of the
primary threats to the subspecies
(predation by nonnative species,
poaching, and habitat loss), predation
by nonnative species is thought to be
occurring now, and predation likely has
been occurring for several decades. This
predation may be an important
impediment to increasing the
population. Predation by introduced
species has played a significant role in
reducing, limiting, and extirpating
populations of island birds, especially
ground-nesters, in the Pacific and other
locations worldwide. Nonnative
predators known or thought to occur in
the range of the friendly ground-dove in
American Samoa are feral cats (Felis
catus), Polynesian rats (Rattus exulans),
black rats (R. rattus), and Norway rats
(R. norvegicus).
In February of 2005, a hurricane
destroyed the habitat of G. stairi in an
area on Olosega Island where the
species had been most frequently
recorded. Although this species has
coexisted with severe storms for
millennia, this example illustrates the
potential for natural disturbance to
exacerbate the effect of anthropogenic
disturbance on small populations.
Consistent monitoring using a variety of
methods over the last 5 years yielded
few observations of this taxon in
American Samoa. The total population
size is poorly known, but is unlikely to
number more than a few hundred pairs.
The distribution of the friendly grounddove is limited to forested slopes with
an open understory and a substrate of
fine scree or exposed earth; this habitat
is not common in American Samoa. We
revised the listing priority number from
a 3 to a 6 to better reflect the fact that
the threats posed to the friendly grounddove (its small population size and
nonnative predators) are nonimminent
but still may occur throughout its range.
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Streaked horned lark (Eremophila
alpestris strigata)—The following
information is based on information
contained in our files. No new
information was provided in the
petition received December 11, 2002.
The streaked horned lark occurs in
British Columbia (Canada), Washington
State, and Oregon. The streaked horned
lark nests on the ground in sparsely
vegetated sites in short-grass dominated
habitats, such as native prairies, coastal
dunes, fallow agricultural fields, lightly
to moderately grazed pastures, seasonal
mudflats, airports, and dredged-material
formed islands in the Columbia River. It
is essentially extirpated from Canada. In
Washington State, surveys show that
there are approximately 380 remaining
breeding birds (Pearson and Altman
2005). In Oregon, the breeding
population is estimated to be
approximately 400 birds.
The streaked horned lark’s breeding
habitat is threatened by loss and
degradation due to conversion of native
grasslands to other uses (such as
agriculture, homes, recreational areas,
and industry), encroachment of woody
vegetation, and invasion of nonnative
plant species (e.g., Scot’s broom and
sod-forming grasses). Native prairies
have been nearly eliminated throughout
the range of the species. It is estimated
that less than 1 to 3 percent of the native
grassland and savanna remains. Those
that remain have been invaded by
nonnative sod-forming grasses. Coastal
nesting areas have suffered the same
fate. Wintering habitats are seemingly
few, and susceptible to unpredictable
conversion to unsuitable overwintering
habitat. Where larks inhabit nonnative
habitats similar in structure to native
prairies (such as airports, military
reservations, agricultural fields, and
dredge formed islands), they are
subjected to a variety of unintentional
human disturbances such as mowing,
recreational and military activities,
plowing, flooding, and dredge spoil
dumping during the nesting season, as
well as intentional disturbances such as
at the McChord AFB where falcons and
dogs are used to haze the birds in order
to avoid aircraft collisions. In some
areas, landowners have taken steps to
improve streaked horned lark nesting
habitat.
The magnitude of threat is high due
to small populations with low genetic
diversity and patchy and isolated
habitats in areas desirable for
development. The threat of invasive
plant species is high and constant. The
numbers of individuals are low and the
numbers of populations are few.
Overwintering birds are concentrated in
larger flocks and subject to
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unpredictable wintering habitat loss,
potentially affecting a large portion of
the population at one time. In
Washington, known populations occur
on airports and two military bases
where management and training
activities can negatively affect streaked
horned lark breeding. In British
Columbia, the one potentially remaining
site with breeding birds occurs at an
airport. The immediacy of threat is
imminent, due to the continued loss of
suitable lark habitat, risks to the
wintering populations, plans for
development on and adjacent to two of
its nesting areas, use of falcons and dogs
to haze breeding birds at McChord AFB,
planned expansions of the McChord
AFB west ramp and Olympia airport,
the planned addition of 130 more
helicopters at the Gray Army Airfield,
and annual Air Force military training
and fire bombing on top of lark nesting
habitat. Because of the increased
imminence of threats, we changed the
listing priority number for the streaked
horned lark from 6 to 3.
Reptiles
Black pine snake (Pituophis
melanoleucus lodingi)— There are
historical records for the black pine
snake from one parish in Louisiana, 14
counties in Mississippi, and 3 counties
in Alabama west of the Mobile River
Delta. Black pine snake surveys and
trapping indicate that this species has
been extirpated from Louisiana and
from 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 on the
DeSoto National Forest. Populations
occurring on properties managed by city
and State agencies as gopher tortoise
mitigation banks or wildlife
management areas represent the best
opportunities for long-term survival of
the species in Alabama. 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 the imminent
threat of high magnitude caused by the
past destruction of most of the longleaf
pine habitat of the black pine snake, and
the continuing persistent degradation of
what remains, we assigned a listing
priority number of 3 to this subspecies.
Although there is no actual change in
threats over the past year, habitat loss
represents an ongoing or imminent
threat to the black pine snake.
Therefore, to help ensure consistency in
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the application of our listing priority
process, we changed the listing priority
number from a 6 to a 3 to reflect that
the threats are imminent.
Louisiana pine snake (Pituophis
ruthveni)—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 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 affect Louisiana pine snake
population and community structure.
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. The pro-active partnerships
to address key management concerns
and research needs are growing and
these conservation efforts have reduced
the magnitude of the threats from high
to moderate. However, the primary
threat from habitat loss continues and
is, therefore, imminent. Thus, based on
threats of moderate to low magnitude
that are imminent, we have changed the
listing priority number from a 5 to an 8.
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Amphibians
Relict leopard frog (Rana onca)—This
leopard frog was considered extinct
since the 1950s, until it was
rediscovered in two relatively small
areas in southern Nevada and a spring
in extreme northwestern Arizona. We
estimate that the current distribution of
the species is 10 to 20 percent of its
historical distribution. Habitat
conversion to agriculture, water
diversions, habitat fragmentation such
as construction of Hoover Dam and
creation of Lake Mead and Lake Mojave,
and introduction and establishment of
nonnative predators and competitors are
believed to be the primary causes of
historical population declines and
reduction in the range and distribution
of the frog. Currently, the primary
threats are low numbers of individuals
and populations, nonnative predators
and competitors, and the potential for
water diversion or ground water
pumping. A conservation agreement and
strategy completed in 2005 will serve as
the management plan for the species. As
prescribed in the agreement and
strategy, annual work plans will be
developed and implemented to monitor
threats and the status of the species as
well as accomplish conservation actions
for the species. The magnitude of
existing threats is moderate, which we
lowered from the previous
determination of high magnitude in
2005. This change in magnitude is
largely based on successful captiverearing and translocation efforts. These
threats remain nonimminent since there
are no known projects or actions that
would adversely affect frog populations
or threaten surface water associated
with known sites occupied by the frog.
Thus, we changed the listing priority
number from a 5 to an 11 for this
species.
Fishes
Cumberland darter (Etheostoma
susanae)—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 fish species is an
approximately 3-inch member of the
family Percidae that is endemic to the
upper Cumberland River system (above
Cumberland Falls) in Kentucky and
Tennessee. Currently, the species is
restricted to 16 headwater streams in
Kentucky and 2 streams in Tennessee.
Within these streams, the Cumberland
darter inhabits low-velocity, shallow
riffles and backwater areas of moderateto low-gradient stream reaches with
stable sand or sandy-gravel substrates.
The primary threat to the species is
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siltation of instream habitats caused by
coal mining activities, silvicultural
practices, road construction, and urban
development. Because the species is
limited to only 18 known populations,
the magnitude of threat for the species
is high; these populations are isolated
from one another by poor-quality
habitat, impoundments, or natural
barriers. The immediacy of threat is
nonimminent because (1) Federal and
State water quality laws have reduced
water quality and habitat threats to
some degree, (2) non-point pollution
threats and modification of reach
geomorphology and hydrology are
cumulative and gradual, and (3)
approximately 40 percent of watersheds
supporting the species are provided
habitat and water quality protection
through Federal ownership (Daniel
Boone National Forest). Consequently,
we assigned a listing priority number of
5 to this species. This represents a
change in the previous listing priority
number, from 6 to 5, due to a change in
taxonomic status for the species, not
because of a change in threat magnitude
or imminence. The Cumberland Johnny
darter, E. nigrum susanae, was elevated
to specific status (E. susanae,
Cumberland darter) based on new
molecular evidence showing that this
subspecies has distinct mitochondrial
DNA haplotypes not found in the
Johnny darter, E. nigrum nigrum.
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.
This species is endemic to upland
portions of the Black Warrior River
system in Alabama where it occurs in
shallow headwater streams. This species
is uncommon and sporadic within its
range, as it favors shallow, flowing
water in spring runs and springassociated streams with emergent
vegetation. Only three disjunct
populations are known: One in the Clear
Creek system in Winston County, one in
spring-fed tributaries of Turkey Creek in
Jefferson County; and one population in
Little Cove Creek (Cove Springs) in
Etowah County.
The Jefferson County population
(Turkey Creek), which is located in a
large metropolitan area, is threatened by
urbanization and commercialization of
its habitat. Siltation from bridge, road,
and sewer line construction has been
recently documented within the Turkey
Creek watershed by academic
researchers and Service biologists. The
major threat to the Winston County
population of rush darters is erosion in
Mill Creek, Doe Branch, and Wildcat
Branch, and the cumulative increase of
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sediments caused from gravel roads and
roadside ditches. Within the past year,
biologists have observed increased
erosion along roads adjacent to Doe and
Wildcat Branches which resulted in
increased siltation within those streams.
Increased urbanization, road
maintenance and silviculture practices
contribute to increased sedimentation in
the watershed. The major threat to the
Cove Springs population is
contamination of the water with
chlorine. Efforts are underway to
improve habitat and water quality;
however, at this time all populations are
being negatively affected by declining
water quality. The magnitude of threat
is high due to the limited number of
populations. We changed the listing
priority from a 5 to a 2 based on the
imminent threat; the threat is imminent
because water quality is currently
declining for all populations.
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Clams
Altamaha spinymussel (Elliptio
spinosa)—The following summary is
based on information in our files. The
Altamaha spinymussel is a freshwater
mussel endemic to the Altamaha River
drainage of southeastern Georgia. The
historical range 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
species is associated with stable, coarse
to fine sandy sediments of sandbars and
sloughs and appears to be restricted to
swiftly flowing water. The species
appears to be extirpated from the
Ohoopee and Oconee Rivers, and its
numbers are greatly reduced in the
Ocmulgee and Altamaha Rivers.
Altamaha spinymussels face severe
habitat degradation from a number of
sources. Primary among these are
threats from sedimentation and
contaminants within the rivers that the
Altamaha spinymussel inhabits. A new
threat of deadhead logging has recently
emerged. These threats to the Altamaha
spinymussel are further compounded by
its limited distribution and the low
population size identified in recent
survey efforts. Efforts to identify the
host fish and expand our understanding
of the spinymussels’ life cycle have not
produced results, attempts to investigate
potential impacts caused by heavy
metals have not received funding, a
survey conducted in 2004 in the
Ocmulgee found no spinymussels, and
deadhead logging presents an added
threat. Consequently, we now consider
the threats to be imminent and have
changed the listing priority number
from a 5 to a 2 for this species.
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Insects
Wekiu bug (Nysius wekiuicola)—The
wekiu bug belongs to the true bug
family, Lygaeidae, and is endemic to the
island of Hawaii. This species only
occurs on the summit of Mauna Kea and
feeds upon other insect species which
are blown to the summit of this large
volcano. The wekiu bug is primarily
threatened by the loss of its habitat from
astronomy development. In 2004 and
early 2005, surveys were conducted that
found multiple new locations of the
wekiu bug on Mauna Kea summit.
Several of these cinder cones within the
Mauna Kea Science Reserve, as well as
two other cinder cones located in the
State Ice Age Natural Area Reserve, are
not currently undergoing development
nor is development planned. With the
discovery of these new locations, the
threats, though ongoing, do not occur
across the entire range of the wekiu bug.
The immediacy of the threats is
imminent in some part of the weiku
bug’s range because ongoing
development is occurring in the Keck
Observatory Outrigger telescope project
area. This development will establish
six new interferometry telescopes
around the existing Keck facility. A
mitigation plan is in place that will
require a 3:1 replacement of damaged
habitat. However, the effectiveness of
this mitigation is untested and
unknown. Although the threats are
ongoing in some areas of wekiu bug
habitat, the recent discoveries of new
locations of the wekiu bug in areas that
are not subject to the primary threat of
astronomy development reduces the
magnitude of the threat from high to
moderate. Therefore, we are changing
the listing priority number for this
species from a 2 to an 8.
Crustaceans
Anchialine pool shrimp (Vetericaris
chaceorum)—Vetericaris chaceorum is
an anchialine pool-inhabiting species of
shrimp belonging to the family,
Procarididae; it is the only species in its
genus. This species is endemic to the
Hawaiian Islands and is only known
from one population in a single pool on
the island of Hawaii. There are two
primary threats to this species. First,
fish do not naturally occur in the pool
inhabited by the species, and it would
be highly vulnerable to predation by any
intentionally or accidentally introduced
fish. Anchialine pools have been used to
discard or hold bait-fish and/or
aquarium fish. Second, the species is
vulnerable to habitat loss due to
degradation by dumping or fill, or
recreational activities. This activity has
occurred in the past but this pool now
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lies within lands administered by the
State of Hawaii Department of Hawaiian
Home Lands. There are no conservation
efforts underway to eliminate the
potential for any of these threats. The
magnitude of threats remains high
because of the devastating effect that
realization of these threats could have
on the species because of its restriction
to a single pool. However, we changed
the listing priority number for this
species from a 1 to a 4 because the
threats are nonimminent: Fish have not
been introduced into the pool (nor is
there any reason to believe that
introduction is imminent) and a site
visit in early 2005 showed there were no
signs of dumping or fill.
Anchialine pool shrimp (Metabetaeus
lohena)—Metabetaeus lohena is an
anchialine pool inhabiting species of
shrimp belonging to the family
Alpheidae. This species is endemic to
the Hawaiian Islands and is currently
known from populations on the islands
of Oahu, Maui, and Hawaii. The
primary threats to this species are
predation by fish (which do not
naturally occur in the pools inhabited
by this species) and habitat loss from
degradation. The pools where this
species occurs on Maui and Hawaii are
located within State Natural Area
Reserves (NAR). Hawaii’s State statutes
prohibit the collection of the species
and the disturbance of the pools in State
NARs. However, enforcement of these
prohibitions is difficult and the negative
effects from the introduction of fish are
extensive and happen quickly.
Therefore, threats to this species are of
a high magnitude. However, we now
consider the threat of predation from
fish to be nonimminent because no fish
were observed during the surveys
conducted in the NARs for this shrimp
in 2004 and no recent habitat
degradation has occurred. In addition,
no nonnative fish were observed during
several site visits to the Oahu location
in 2005. Therefore, we changed the
listing priority number of this species
from a 2 to a 5.
Anchialine pool shrimp
(Palaemonella burnsi)—Palaemonella
burnsi is an anchialine pool inhabiting
species of shrimp belonging to the
family, Palaemonidae. This species is
endemic to the Hawaiian Islands and is
currently known from three populations
on the island of Maui and one
population on the island of Hawaii. The
primary threats to this species are
predation by fish (which do not
naturally occur in the pools inhabited
by this species) and habitat loss due to
degradation. The pools where this
species occurs on Maui are located
within a State Natural Area Reserve
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(NAR). Hawaii’s State statutes prohibit
the collection of the species and the
disturbance of the pools in State NARs.
On the island of Hawaii, the species
occurs within a National Park and
collection and disturbance are also
prohibited. However, enforcement of
these prohibitions is difficult, and the
negative effects from the introduction of
fish are extensive and happen quickly.
Therefore, threats to this species are of
high magnitude. However, we no longer
consider the threats to be imminent,
because during a 2004 survey no fish
were observed in the pools where these
shrimp occur on Maui or the island of
Hawaii and there was no evidence of
recent habitat degradation. Therefore,
the threats of predation from fish and
habitat degradation are nonimminent,
and consequently we changed the
listing priority number of this species
from a 2 to a 5.
Anchialine pool shrimp (Procaris
hawaiana)—Procaris hawaiana is an
anchialine pool inhabiting species of
shrimp belonging to the family,
Procarididae. This species is endemic to
the Hawaiian Islands and is currently
known from two populations on the
island of Maui and one population on
the island of Hawaii. The primary
threats to this species are predation
from fish (which do not naturally occur
in the pools inhabited by this species)
and habitat loss due to degradation. The
pools where this species occurs on Maui
are located within a State Natural Area
Reserve (NAR). Hawaii’s State statutes
prohibit the collection of the species
and the disturbance of the pools in State
NARs. However, enforcement of these
prohibitions is difficult and the negative
effects from the introduction of fish are
extensive and happen quickly. There are
no conservation efforts underway to
alleviate the potential for any of these
threats in the one pool on the island of
Hawaii. Therefore, threats to this
species remain at high magnitude.
However, we no longer consider the
threats to be imminent because, during
a 2004 survey, no fish were observed in
the pools where these shrimp occur on
Maui or the island of Hawaii. In
addition, there were no signs of
dumping or fill on a site visit to the
location on the island of Hawaii in early
2005. Therefore, we changed the listing
priority number of this species from a 2
to a 5.
Flowering plants
Abronia alpina (Ramshaw Meadows
sand-verbena)—Abronia alpina is a
small perennial herb, 2.5 to 15.2
centimeters (1 to 6 inches) across
forming compact mats with lavenderpink, trumpet-shaped, and generally
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fragment flowers. Abronia alpina is
known from one main population center
in Ramshaw Meadow on the Kern
Plateau of the Sierra Nevada, California
and from one subpopulation found in
adjacent Templeton Meadow. The total
estimated area occupied is
approximately 6 hectares (15 acres).
Population estimates from 1985–1994
range from a low of 69,652 plants in
1986 to 132,215 plants in 1987. Surveys
conducted since 1994 indicate that no
significant changes have occurred in
population size or location, although,
the 2003 survey showed population
numbers to be at the low end of the
range. The population fluctuates from
year to year without any clear trends.
The major threats facing A. alpina
include habitat disturbance and
trampling from incidental livestock
trailing, pack animals, and hikers;
campsite development; and erosion
associated with such disturbances. An
additional threat is encroachment of
lodgepole pine into areas occupied by
the species. Lodgepole pine
encroachment has altered the meadow
and becoming established within A.
alpina habitat. Lodgepole pine
encroachment may alter soil
characteristics by increasing organic
matter levels, decreasing porosity, and
moderating diurnal temperature
fluctuations thus reducing the
competitive ability of A. alpina to
persist in an environment more
hospitable to other plant species. The
Ramshaw Meadow ecosystem is subject
to alteration by lowering of the water
table due to downcutting of the South
Fork of the Kern River (SFKR). The
SFKR flows through Ramshaw Meadow,
at times coming within 15 meters (50
feet) of A. alpina habitat, particularly in
the vicinity of five subpopulations. The
habitat occupied by A. alpina directly
borders the meadow system supported
by the SFKR. Drying out of the meadow
system could affect A. alpina pollinators
and/or seed dispersal agents.
Established hiker, packstock, and cattle
trails pass through A. alpina
subpopulations. Two main hiker trails
pass through Ramshaw Meadow, but
were rerouted out of A. alpina
subpopulations where feasible, in 1988
and 1997. Remnants of cattle trails that
pass through subpopulations in several
places receive occasional incidental use
by horses and sometimes hikers. In
2001, the U.S. Forest Service
discontinued grazing on the Templeton
allotment, which includes Ramshaw
Meadow, for a period of 10 years.
Consequently, livestock grazing does
not currently occur in the two meadow
areas where the species is found.
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However, the Forest Service could
change their decision when the 10-year
period ends and livestock grazing
within A. alpina habitat may resume. To
ensure consistency in our interpretation
of the imminence of threats, we revised
the listing priority for A. alpina from an
11 to an 8 to reflect the fact that most
of these moderate threats are imminent.
Arabis georgiana (Georgia
rockcress)—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 nonnative weeds,
especially Japanese honeysuckle
(Lonicera japonica), in this species’
habitat. Eight populations are currently
or potentially threatened by the
presence of nonnative plants. The
heritage programs in Alabama and
Georgia have initiated plans for exotic
control at several populations. The
magnitude of threats to this species is
moderate to low due to the number of
populations (18) across multiple
counties in two states and the insidious
nature of the threats. However, since a
number of the populations are currently
being impacted by nonnative plants, we
now consider the threats to be
imminent. Thus, we changed the listing
priority number from an 11 to an 8 for
this species.
Astralagus toritpes (Sleeping Ute
milkvetch)—The following information
is based on information contained in
our files. Sleeping Ute milkvetch is a
perennial plant that grows only on the
Smokey Hills layer of the Mancos Shale
Formation on the Ute Mountain Ute
Indian Reservation in Montezuma
County, Colorado. In 2000, 3,744 plants
were recorded at 24 locations covering
500 acres within an overall range of
64,000 acres. Available information
from 2000 indicates that the species
remains stable. Threats from borrow pit
excavation, off-highway vehicles,
irrigation canal construction, and a
prairie dog colony have had minor
impacts that reduced the range and
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number of plants by small amounts in
the past and are potential future threats.
Off-highway vehicle use of the habitat is
reportedly increasing but we do not
have direct evidence of this. Oil and gas
development is active in the general
area, but we have received no
information from the tribe to indicate
whether there is development within
the habitat for the plants on their land.
Because the threats are nonimminent,
we changed the listing priority number
for Sleeping Ute milkvetch from 8 to 11.
Bidens campylotheca ssp. waihoiensis
(Kookoolau)—The following
information is based on information
contained in our files. Kookoolau is an
erect, perennial found in wet AcaciaMetrosideros (koa-ohia) forest on Maui,
Hawaii. Bidens campylotheca ssp.
waihoiensis is known from one
population of 200 individuals. It is
threatened by cattle, which eat this
plant, and degrade and destroy habitat.
The area in which all individuals of this
subspecies are currently found is fenced
and cattle have been removed. The
threats remain of high magnitude, but
predation, and habitat degradation and
destruction by feral cattle are no longer
imminent because they are not currently
occurring. Therefore, we have changed
the listing priority number for this
species from 3 to 6.
Castilleja christii (Christ’s
paintbrush)—The following information
is based on information contained in
our files. This species of paintbrush is
found in one population on the summit
of Mount Harrison in Cassia County,
Idaho. This endemic species is
considered a hemiparasite and it grows
in association with subalpine meadow
and sagebrush habitats. The population
found on 85 ha (220 ac) may be large in
number (greater than 10,000 individual
plants), but, current population
estimates are not available. Monitoring
indicates that reproductive stems per
plant and plant density have decreased
significantly since 1995. Although these
trends were upward between 2004 and
2005, it is not known if that trend will
continue. The habitat on Mount
Harrison is bisected by several roads,
has been until recently utilized by
unauthorized livestock, and is subject to
a high degree of recreational use.
However, these threats occur seasonally
during the growing season, in latespring and summer periods, and they
are currently being controlled by the
U.S. Forest Service with fencing, rock
barriers, and interpretative signs. The
largest threat to the species is from
nonnative invasive plants, the majority
of which are smooth brome (Bromus
inermis). The smooth brome infestation
was treated in 2003, 2004, and 2005 by
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the U.S. Forest Service. The success of
treating smooth brome that was present
in 13.6 percent of the range of C. christii
in 2005 will not be known immediately,
although there is a commitment in a
recently signed Conservation Agreement
by the U.S. Forest Service and U.S. Fish
and Wildlife Service to continue these
efforts until they are successful or for
the next 10 years. The magnitude of the
threats with these conservation
measures appears low at this time.
However, the smooth brome continues
to threaten the habitat for C. christii
despite control efforts. Plant monitoring
transects still contained significant
densities of smooth brome following the
eradication efforts in 2005. This threat
from smooth brome is imminent
because this threat still persists in levels
that affect the native plant community
that provides habitat for C. christii.
Thus, we changed the listing priority
number from an 11 to an 8 for this
species since the threats are imminent.
Chamaesyce deltoidea pinetorum
(Pineland sandmat)—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
largest population of the pineland
sandmat, estimated at approximately
10,000 plants, is located on Long Pine
Key within Everglades National Park.
All other populations of the pineland
sandmat are smaller and occur on
isolated pine rockland fragments in
heavily urbanized Miami-Dade County.
Those populations on private lands are
at risk from development and habitat
degradation. Populations on most public
and private lands in urban Miami-Dade
County are inherently vulnerable to
invasion by exotic plants, fire
suppression or inadequate prescribed
fire, and limited management. Overall,
the magnitude of threats to this species
is moderate since by applying regular
prescribed fire, the National Park
Service has kept Long Pine Key’s
pineland vegetation intact and relatively
free of exotic pest plants. In addition,
after a thorough review of the status and
threats to the pineland sandmat, we
determined that the threats are nonimminent. Therefore, we changed the
listing priority number from a 9 to a 12
for this subspecies.
Erigeron lemmonii (Lemmon
fleabane)—The following summary is
based on information contained in our
files and the petition received in July of
1975. The species is known from one
site in a canyon in the Fort Huachuca
Military Reservation of southeastern
Arizona. As of 1991, approximately 400
plants were known from this site. No
formal surveys have been done since
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that time, but the population seemed
stable throughout the 1990s. The threats
to this species are from catastrophic
wildfire in the canyon and on-going
drought conditions. We do not know if
this species has any adaptations to fire.
Due to its location on cliffs, we suspect
that fires that may have occurred at
more regular intervals and burned at
low intensities may have had little to no
effect on this species. It is due only to
lack of fire and the accumulated fuel
load that the fire intensity and
associated heat may be high enough to
damage or kill plants on adjacent cliffs,
especially near the ground. On the other
hand, the plants that are much higher
on the cliff face would probably not be
affected. Ft. Huachuca has indicated a
willingness to develop a conservation
agreement for this species. We now
consider the magnitude of threats to be
moderate rather than high because we
believe that not all of the population
would be adversely affected by a
wildfire or drought. The threats are still
imminent because the likelihood of a
fire is high. Therefore, we changed the
listing priority number from a 5 to an 8
due to moderate, imminent threats.
Geranium hanaense (Nohoanu)—This
species is a decumbent shrub found in
bogs on Maui, Hawaii. This species is
known from one population with 300 to
500 individuals. Geranium hanaense is
threatened by pigs that degrade and
destroy habitat, and by nonnative plants
that outcompete and displace it.
However, feral pigs have been fenced
out of and removed from both bogs in
which this species currently occurs, and
a control program has reduced
nonnative plants in all fenced areas.
This changes the immediacy of the
threats form imminent to nonimminent.
Therefore, we have changed the listing
priority number for this species from 2
to 5.
Geranium kauaiense (Nohoanu)—
Nohoanu 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. Geranium kauaiense is threatened
by pigs that directly prey upon it,
degrade and destroy habitat, and by
nonnative plants that outcompete and
displace it. Feral pigs have been fenced
out of the three bogs where G. kauaiense
currently occurs, and nonnative plants
have been greatly reduced in all three
fenced bogs, and are not found in the
immediate vicinity of any G. kauaiense
individuals. Because these threats are of
high magnitude but no longer are
imminent, we have changed the listing
priority number from 2 to 5.
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Pediocactus peeblesianus var.
fickeiseniae (Fickeisen plains cactus) ‘‘
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 well-drained hills in Navajoan
desert or grassland. In 1999, the Arizona
Game and Fish Department noted 23
occurrences for the species, including
historical ones. The species is located
on BLM, Forest Service, tribal, and
possibly State lands. Recent reports
from the BLM and Navajo Nation
describe populations of the species as
being in decline. The main humaninduced threats to this cactus are offroad vehicles and trampling associated
with livestock grazing. Monitoring data
has detected mortality associated with
livestock grazing. Illegal collection of
this species has been noted in the past,
but we do not know if it is a continuing
threat. The populations that have been
monitored have been affected, in part,
by the continuing drought. There has
been very low recruitment and rabbits
and rodents have consumed adult plants
since there is reduced forage available
during these dry conditions. In our prior
assessments, we concluded that threats
were not imminent. However, using a
consistent interpretation of imminence
related to whether threats are on-going,
we are correcting our ranking to reflect
that the threats are imminent. As a
result, we changed the LPN for this
plant variety from a 6 to a 3.
Potentilla basaltica (Soldier Meadow
cinquefoil or basalt cinquefoil)—Soldier
Meadow cinquefoil is a low growing,
rhizomatous, herbaceous perennial that
is associated with alkali meadows,
seeps, and occasionally marsh habitats
bordering perennial thermal springs,
outflows, and meadow depressions. In
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. The California population
occupies less than an acre on private
lands and supports fewer than 1,000
plants.
The species and its habitat are
threatened by increasing recreational
use in the areas where it occurs as well
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as historic livestock grazing and
activities associated with the use of
authorized and unauthorized roads.
Conservation measures implemented
recently by the Bureau of Land
Management include the installation of
fencing to exclude livestock wild
horses, burros and other large mammals;
closing of access roads to spring,
riparian, and wetland areas and the
limiting of vehicles to designated routes;
the establishment of a designated
campground away from the habitats of
sensitive species; the installation of
educational signage and, an increased
staff presence, including law
enforcement and a volunteer site
steward during the six-month period of
peak visitor use. These conservation
measures have reduced the magnitude
of threat to the species from high to
moderate; all remaining threats are
nonimminent and involve long-term
changes to the habitat for the species
resulting from past impacts. In
consideration of these conservation
measures, we lowered the listing
priority number from 5 to 11.
Other Taxonomic Changes in
Candidates
Flowering Plants
Physaria 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 species is in the Cruciferae
(Mustard family). Historically and
currently, White Bluffs bladder-pod has
only been known from a single
population that occurs along the White
Bluffs of the Columbia River in Franklin
County, Washington. Physaria
tuplashensis was originally described as
Lesquerella tuplashensis in 1996, which
is the name we have used for it in prior
CNORs. In 2002, there was a suggestion
that the Lesquerella and Physaria genera
should be united as Physaria, and that
L. tuplashensis should be reduced to P.
douglasii subspecies tuplashensis. A
recent study (2005) recommended
accepting the new genus name of
Physaria and, supported by
metamorphic work, proposed retaining
full species status for the taxon, and a
new nomenclature: Physaria
tuplashensis. We recognize this new
nomenclature in this notice. There are
no changes in the magnitude or
imminence of threats to the taxon, so we
continue to assign a listing priority
number of 5 to this species.
Candidate Removals
As summarized below, we have
evaluated the threats to the following 10
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species and considered factors that,
individually and in combination,
presently or potentially could pose a
risk to these species and their habitat.
After a review of the best available
scientific and commercial data, we
conclude that listing these 10 species
under the Endangered Species Act is not
warranted because the species are not
likely to become endangered species
within the foreseeable future throughout
all or a significant portion of their range.
Therefore, we find that proposing a rule
to list these species is not warranted,
and we no longer consider them to be
candidate species for listing. We will
continue to monitor the status of these
species, and to accept additional
information and comments concerning
this finding. We will reconsider this
determination in the event that new
information indicates that the threats to
these species are of a considerably
greater magnitude or imminence than
identified through assessments of
information in our files, as summarized
here. The summary below also notes
four other species for which we
published separate findings removing
them from candidate status since the
most recent CNOR.
Birds
Many-colored fruit-dove (Ptilinopus
perousii perousii)—The following
summary is based on information
contained in our files. P. p. perousii, is
found in American Samoa on the four
main islands of Tutuila, Olosega, Ofu,
and Tau, and in Independent Samoa. It
is primarily associated with mature
rainforest habitat. The many-colored
fruit-dove is highly mobile and may
travel large distances, presumably in
search of fruiting banyans (Ficus prolixa
and F. obliqua). The American Samoa
population of P. p. perousii is the only
population of this subspecies under U.S.
jurisdiction. The primary threats we
recognized in the past are its small
population size, stochastic natural
disturbances such as hurricanes, the
accidental introduction of new
pathogens or parasites, and possibly
predation by introduced mammalian
predators. We previously assigned a
listing priority number of 12 to this
taxon, reflecting threats that we
determined were of low magnitude and
not imminent. Five years of monitoring
documented an increase in the relative
abundance of the subspecies prior to
Hurricane Heta in January of 2004 and
Hurricane Olaf in February 2005. The
upward trend has been stalled by these
severe storms, but continued monitoring
should indicate whether (as we expect)
effects of the 2004 and 2005 hurricanes
have caused a temporary, but natural,
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interruption in the trend of increase, or
whether hurricane effects have reversed
this trend. Avian malaria, once thought
to possibly pose a threat to this
subspecies, likely is not pathogenic in
Samoa. The stable distribution of the
subspecies and recent documented
increase in relative abundance in
American Samoa suggest that the threats
summarized above currently are not
having a detrimental effect on the
subspecies’ overall population, and it is
unlikely to become endangered within
the foreseeable future. Therefore, listing
is not warranted.
Gunnison sage-grouse (Centrocercus
minimus)—See separate revised 12month petition finding published in the
Federal Register on April 18, 2006 (71
FR 19953).
Reptiles
Cagle’s map turtle (Graptemys
caglei)—The following information is
based on information contained in our
files, including information from the
petition received April 26, 1991. Cagle’s
map turtle occurs in scattered sites in
seven counties in Texas on the
Guadalupe, San Marcos, and Blanco
Rivers. We previously identified loss
and degradation of riverine habitat from
large and small impoundments (dams or
reservoirs) as 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. In the past, construction of
smaller impoundments and human
activities on the rivers known to be
occupied by the Cagle’s map turtle have
likely eliminated or reduced foraging
and basking habitats. Currently, there
are no firm plans for reservoirs in the
Guadalupe-San Antonio River System.
Cagle’s map turtle is also vulnerable to
overcollecting and target shooting but
actions taken by Texas Parks and
Wildlife Department (TPWD) have
increased protection of the species
against collecting and shooting. Cagle’s
map turtle was listed as threatened by
TPWD, effective November 16, 2000,
and TPWD regulations prohibit the
taking, possession, transportation, or
sale of any of the animal species
designated by state law as endangered
or threatened without the issuance of a
permit. Estimates of population
numbers of the species in the
Guadalupe and San Marcos Rivers in
1991 and 2001 indicates an overall
population increase, although estimated
populations at some sites declined.
Because of stable population size,
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increased protection, and no foreseeable
threats from reservoir construction, we
find that listing Cagle’s map turtle is not
warranted.
Amphibians
Boreal toad (Southern Rocky
Mountains DPS) (Bufo boreas boreas)—
see separate revised 12-month petition
finding published in the Federal
Register on September 29, 2005 (70 FR
56880).
Insects
Lesser Adams Cave beetle
(Pseudanophthalmus cataryctos
Krekeler) and Greater Adams Cave
beetle (P. pholeter Krekeler)—see
Federal Register notice published on
December 8, 2005 (70 FR 72973).
Po’olanui gall fly (Phaeogramma
sp.)—Because there is no published
name or description for this fly, this
taxa is not considered valid and does
not meet the Act’s definition of a
species and is not eligible for listing.
Therefore, we find that listing is not
warranted.
Crustaceans
Anchialine pool shrimp (Antecaridina
lauensis)—This species has a disjunct,
Indo-Pacific distribution. It has been
reported from the Fiji Islands,
Mozambique Channel (Madagascar), the
Red Sea-Dahlak, Ryukyu and Daito
Islands (Japan), the Solomon Islands
and the Hawaiian Islands. In Hawaii, A.
lauensis is known from two pool groups
on Maui (Ahihi-Kinau State Natural
Area Reserve) and two pools on the
southern end of the island of Hawaii
(Lua o Palahemo, and one on private
land). Like other anchialine pool shrimp
species, it is believed that this species
inhabits an extensive network of waterfilled interstitial spaces (cracks and
crevices) leading to and from the actual
pool, and this trait has precluded
researchers from obtaining population
size estimates during surveys for the
species. In Lua o Palahemo on the
island of Hawaii, A. lauensis co-occurs
with two other candidate species of
anchialine pool shrimp, Procaris
hawaiana and Vetericaris chaceorum,
and with Calliasmata pholidota (see
below).
Although we have information on the
threats to the population in Hawaii,
population numbers and threats to the
species where it occurs elsewhere in the
world are unknown. We find that listing
is not warranted because there is
insufficient information on the species’
status throughout its range to determine
whether it warrants protection under
the Act. We are unable to consider
listing the Hawaii population as a
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distinct population segment since this
animal is not a vertebrate.
Anchialine pool shrimp (Calliasmata
pholidota) ‘‘ This species has a disjunct,
Indo-Pacific distribution. It has been
reported from the Red Sea-Sinai
Peninsula, Funafuti Atoll (Ellice
Islands), and the Hawaiian Islands of
Maui and Hawaii. On the island of
Hawaii, C. pholidota occurs in one pool
at Ka Lae (South Point) at Lua o
Palahemo and in one pool group in the
Manuka Natural Area Reserve (NAR).
On Maui, C. pholidota is found in four
pool groups in the Ahihi-Kinau NAR. At
Lua o Palahemo, C. pholidota co-occurs
with two other candidate species of
anchialine pool shrimp, Procaris
hawaiana and Vetericaris chaceorum,
and with Antecaridina lauensis (see
above). Like other anchialine pool
shrimp species, it is believed that this
species inhabits an extensive network of
water-filled interstitial spaces (cracks
and crevices) leading to and from the
actual pool, and this trait has precluded
researchers from obtaining more
accurate population size estimates
during surveys for the species.
Worldwide species status information,
including population numbers and
threats to the species outside the U.S. is
unknown. We find that listing is not
warranted because there is insufficient
information on the species status
throughout its range to determine
whether this species warrants protection
under the Act. We are unable to
consider listing the Hawaii population
as a distinct population segment since
this animal is not a vertebrate.
Flowering Plants
Aliciella cespitosa (= Gilia caespitosa)
(wonderland alice-flower or Rabbit
Valley gilia)—The wonderland aliceflower (also known as Rabbit Valley
gilia) is a plant within the Phlox family
found in Wayne County, Utah. The
species is primarily associated with
sand-filled pockets and crevices of
Navajo Sandstone on slopes having
mechanical weathering or erosion of
rock in pinyon-juniper/mountain
mahogany vegetation communities
between 5,200 and 9,000 feet in
elevation.
This species occurs in more sites and
is much more abundant than was
initially thought. In 1996 we knew of 6
population areas with an estimated total
of 5,000 plants. However, increased
surveys from 2000 to 2003 identified 50
known sites at the 6 population areas,
with an estimated 25,350 individual
plants. For the past several years our
assessments of this species concluded
that threats were moderate to low and
were nonimminent, and we assigned it
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a listing priority number of 11. We
identified potential collection of plants
and seeds as a significant threat.
However, we have no evidence that
collection is occurring, or if it is
occurring that it is impacting the overall
status of the species. We also have no
information to suggest that collection in
the future is likely to put populations at
risk at any of the sites currently known
to be occupied. Other threats we
identified included impacts associated
with recreational trails, off-road vehicle
use, livestock trampling, and low
natural recruitment. Although some of
these threats are ongoing, they are
localized, and appear to have little
impact. The majority of sites are not
easily accessible, and the factors that
currently or potential could impact
individuals have not been shown to
affect the species rangewide, nor do we
expect that to become the case. In
addition, a Conservation Agreement and
Strategy, signed in 1996 and currently
being updated, promotes continued
cooperation among the agencies and
helps to direct a variety of conservation
actions, including: Inventory remaining
suitable habitats; identify research
needs and conduct studies; refine
monitoring protocols; continue
monitoring; implement land
management policies and regulations for
protection of Navajo endemic plant
species; and continue to pursue public
awareness opportunities. Based on our
updated assessment, we find that listing
this species is not warranted.
Astragalus equisolensis (horseshoe
milkvetch)—Horseshoe milkvetch is a
plant in the pea family and is found on
the Duchesne River Formation in Uintah
county, Utah and Mesa county,
Colorado. It is associated with mixed
desert and salt desert shrub vegetation
communities that are generally
dominated by sagebrush, shadscale and
horsebrush. Surveys in 1992 estimated
the population at 10,000 in Utah and
there is no recent information indicating
it has declined; the Colorado population
is a recent discovery. The only potential
threat of substance is from future energy
development, but that does not threaten
the species through most of its range.
Based on available information,
including the recent discovery of the
species in Colorado and an apparent
low level of potential threat, we do not
have sufficient information to justify a
determination that the species should be
proposed for listing. Therefore, we find
that listing this species is not warranted.
Castilleja aquariensis (Aquarius
paintbrush)—The Aquarius paintbrush
is a plant in the figwort family found
only on the Aquarius plateau of south
central Utah. Habitat characteristics are
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meadow openings and open spruce-fir
stands. A recent survey conducted in
2004 and 2005 counted 74,100
individuals, a much higher number than
earlier estimates. Factors affecting the
species include off-road vehicle use;
wildlife and livestock grazing; predation
by pocket gophers, aphids, crickets and
grasshoppers; and low precipitation.
However, we do not have any evidence
that these factors are a significant threat
to population levels. Therefore, we find
that listing the species is not warranted.
Paronychia congesta (Bushy whitlowwort)—Bushy whitlow-wort is endemic
to Jim Hogg County, Texas, known from
only two populations that occur within
the drainage of two tributaries of the
Arroyo Grande. Historically, this species
was documented only from the type
locality with 2,000 individual plants
counted. A second small population of
100 individuals was found two miles
north-northeast of the type locality in
1987. The two known populations occur
on small areas that cover approximately
5 and 15 acres. Little quantitative data
have been collected for this species,
therefore we do not know whether
populations have expanded or
contracted. The sparse information that
is available suggests the current range
and distribution of the species has not
changed from the historical description.
The types of factors believed to
potentially adversely affect this species
include destruction, modification, and
fragmentation of the habitat, as well as
eradication of individual plants.
However, conversion of rangeland to
residential development is not
considered a significant threat since this
part of southern Texas is not undergoing
rapid residential or industrial
development. The extent of alteration of
the whitlow-wort’s habitat via
conversion of native brush to nonnative
forage grasses is unknown since all of its
habitat is privately owned and not
accessible. Other potential threats
include displacement or destruction of
individual plants by construction
activities associated with highways,
pipeline installation, oil and gas
exploration, well-pad construction and
right-of-way maintenance. However, we
do not have any information on the
likely implementation of these potential
activities and no ongoing imminent
threats have been identified for this
species. We have determined that listing
is not warranted because insufficient
information exists on biological
vulnerability and threats to support a
proposal to list this species.
Sidalcea hickmanii parishii (Parish’s
checkerbloom)—Parish’s checkerbloom
is an herbaceous perennial plant in the
mallow family (Malvaceae), with
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multiple stems emerging annually from
a woody root crown. It most commonly
appears following fires, apparently
having evolved to rapidly take
advantage of unvegetated openings in
forest or chaparral. Most historic
collections, and all currently known
populations, are known from open areas
along roads, trails, firebreaks, small
landslides, or in recently burned areas.
All known populations are on USDA
Forest Service lands. Parish’s
checkerbloom has been collected from
San Bernardino, Santa Barbara, and San
Luis Obispo Counties, California. Its
distribution in San Bernardino County
appears to be particularly restricted,
although the vagueness of historical
location information and the plant’s
emergence primarily following fire
make it difficult to accurately assess its
distribution. The discovery of a new,
albeit small, population found on the
desert-facing slopes of the San
Bernardino Mountains in 2000 suggests
that habitat not previously considered
suitable may in fact be so.
Threats identified for this taxon fall
into two groups—those that negatively
affect individual or small groups of
plants (the ‘‘expressed’’ portions of what
may be larger populations in
seedbanks), and those that have the
potential to substantially alter a large
area of surrounding habitat or damage
any unexpressed seedbanks that may
occur in surrounding soils. Activities in
the former group include livestock
grazing on individual plants along roads
and grading of existing roads. Those in
the later group include altered fire
regimes (e.g. aggressive fire suppression,
prescribed burning in winter or spring),
post-fire livestock grazing, development
or expansion of roads and facilities (e.g.
recreational, military communication
facilities, or development of private
inholdings), and invasion by nonnative
species. The southern portion of this
taxon’s range, in San Bernardino
County, is most vulnerable to these
activities due to its more restricted
distribution there, its closer proximity
to human population centers, and the
area’s greater recreational use.
Review of recent information
indicates the number of populations
located is greater and the known range
of the taxon is larger than we previously
understood. Also, our conclusion
regarding the magnitude and the
immediacy of the threats has shifted
with the additional information we have
about the species. We considered the
magnitude of threats to individuals, as
well as habitat with unexpressed
seedbank, was greater when we only
knew of 3 small extant locations for the
species as compared to now, when we
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are aware of 5 extant locations,
including 1 with a large population. We
also considered the immediacy of the
threats to be greater when we only knew
of 3 small extant locations for the
species. For some human-caused
activities, such as road grading and
construction of fire breaks, we have had
the opportunity to observe that these
activities most likely caused the
expression of a portion of the seedbank,
in a sense providing some of the same
habitat conditions that are provided by
wildfire (removal of litter, scarification
of seed). This suggests that at least
certain human activities can be altered
(such as in timing of grading) so that
they will not negatively impact the
species. Although there is great
uncertainty regarding how and to what
extent future wildfires may release the
seedbank of this species, we do not
believe that the threat from lack of fires
or any human-caused activities are
imminent (as compared to a known
threat from a planned activity with a
definite timeline, such as a housing
development) or substantial. Therefore,
we find that listing is not warranted.
Petition Findings
The Act provides two mechanisms for
considering species for listing. One
method allows the Secretary, on his
own initiative, to identify species for
listing under the standards of section
4(a)(1). We implement this through the
candidate program, discussed above.
The second method for listing a species
provides a mechanism for the public to
petition us to add a species to the Lists.
Under section 4(b)(3)(A), when we
receive such a petition, we must
determine within 90 days, to the
maximum extent practicable, whether
the petition presents substantial
information that listing may be
warranted (a ‘‘90-day finding’’). If we
make a positive 90-day finding, we must
promptly commence a status review of
the species under section 4(b)(3)(A); we
must then make and publish one of
three possible findings within 12
months of the receipt of the petition (a
‘‘12-month finding’’):
1. The petitioned action is not
warranted;
2. The petitioned action is warranted
(in which case we are required to
promptly publish a proposed regulation
to implement the petitioned action;
once we publish a proposed rule for a
species, section 4(b)(5) and 4(b)(6)
govern further procedures regardless of
whether we issued the proposal in
response to a petition); or
3. The petitioned action is warranted
but that (a) the immediate proposal of a
regulation and final promulgation of
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regulation implementing the petitioned
action is precluded by pending
proposals, and (b) expeditious progress
is being made to add qualified species
to the lists of endangered or threatened
species. (We refer to this as a
‘‘warranted-but-precluded finding.’’)
Section 4(b)(3)(C) of the Act requires
that when we make a warranted-butprecluded finding on a petition, we are
to treat such a petition as one that is
resubmitted on the date of such a
finding. Thus, we are required to
publish new 12-month findings on these
‘‘resubmitted’’ petitions on an annual
basis.
On December 5, 1996, we made a final
decision to redefine ‘‘candidate species’’
to mean those species for which the
Service has on file sufficient
information on biological vulnerability
and threat(s) to support issuance of a
proposed rule to list, but for which
issuance of the proposed rule is
precluded (61 FR 64481, December 6,
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
findings, 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
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53769
species’’ for which we have made a
warranted-but-precluded 12-month
finding, and to ‘‘make prompt use of the
[emergency listing] authority [under
section 4(b)(7)] to prevent a significant
risk to the well being of any such
species.’’ The CNOR plays a crucial role
in the monitoring system that we have
implemented for all candidate species
by providing notice that we are actively
seeking information regarding the status
of those species. We review all new
information on candidate species as it
becomes available, prepare an annual
species assessment form that reflects
monitoring results and other new
information, and identify any species
for which emergency listing may be
appropriate. If we determine that
emergency listing is appropriate for any
candidate, whether it was identified
through our own initiative or through
the petition process, we will make
prompt use of the emergency listing
authority under section 4(b)(7). We have
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
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specificity; in the list of species that
were the subject of listing actions that
precluded us from proposing to list
candidate species, we did not state the
specific action at issue for each species
in the list and we did not indicate
which actions were court-ordered.
On June 22, 2004, in a similar case,
the United States District Court for the
Eastern District of California also
concluded that our determination of
preclusion may appropriately be based
on a national analysis (Center for
Biological Diversity v. Norton No. CV 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 drafted the previous CNOR to
address the concerns of these courts and
continue to incorporate those changes
that addressed the courts’ concerns in
this CNOR. 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
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have accomplished does preclude action
on listing candidate species.
Pursuant to section 4(b)(3)(C)(ii) and
the Administrative Procedure Act (5
U.S.C. 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),
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 245
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 two species, the New
England cottontail and the red knot, that
were petitioned prior to this CNOR but
for which we have not already
published a separate warranted-butprecluded 12-month finding. We
previously published a separate
substantial 90-day petition finding for
the New England cottontail (69 FR
39395).
Our review included updating the
status of and threats to petitioned
candidate or listed species for which we
published findings, pursuant to section
4(b)(3)(B), in the previous CNOR. We
have incorporated new information we
gathered since the prior finding and, as
a result of this review, we are making
continued warranted-but-precluded 12month findings on the petitions for
these species.
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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
May 2, 2005, through August 23, 2006.
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 under 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 the listing
priority of a species 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
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violating the Anti-Deficiency Act (31
U.S.C. 1341 (a)(1)(A)). 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 2005,
the costs (excluding publication costs)
for conducting a 12-month finding,
without a proposed rule, ranged from
approximately $11,000 for one species
with a restricted range and involving a
relatively uncomplicated analysis, to
$305,000 for another species that 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, July 1, 1997).
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 and the Courts have in
effect determined, through the listing
cap, the critical habitat subcap, and the
amount of funds needed to address
court-mandated critical habitat
designations, the amount available for
other listing activities. It is this amount
(i.e., the funds in the listing cap other
than those needed to address courtmandated critical habitat for already
listed species) that is used in the
determination here of preclusion and
expeditious progress.
Congress also 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
[i.e., for a lower-ranking species]
unwise.’’ Therefore, in fiscal year 2005,
the outer parameter within which
‘‘expeditious progress’’ must be
measured is that amount of progress that
could be achieved by spending $5.6
million, which included $4.6 million
available in the Listing Program
appropriation not within the critical
habitat subcap plus approximately $1.0
million from the critical habitat subcap
that was not needed to comply with
court orders or court-approved
settlement agreements for critical
habitat designations. The rest of the
critical habitat subcap funds were used
to comply with court orders or courtapproved settlement agreements for
designating critical habitat for
previously listed species, 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
53771
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 (i.e. $5.6 million) was
consumed by such court-mandated
listing activities in FY 2005, and by
ordering or sanctioning these actions the
courts essentially determined that these
were the highest priority actions to be
undertaken with available funding.
Copies 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 December 8, 2004, the President
signed the 2005 Interior and Related
Agencies Appropriations Act (Pub. L.
108–447), which, as a result of the
subcap and subsequent rescissions, in
effect included $4,643,000 for listing
activities not related to critical habitat
designations for species that already are
listed. However, as discussed above, a
relatively small portion of the critical
habitat subcap was used for listing
actions resulting in a total of $5,604,178
being expended for listing actions. This
appropriation was fully allocated to
fund the following categories of actions
in the Listing Program: Essential
litigation-related, and administrativeand program-management functions;
compliance with court orders and courtapproved settlement agreements
requiring that petition findings or listing
determinations be completed by a
specific date; section 4 listing actions
with absolute statutory deadlines; and a
few high-priority listing actions. While
more funds were available in FY 2005
than in previous years to work on listing
actions that were not the subject of
court-orders or court-approved
settlement agreements, based on the
available funds and their allocation for
these purposes, only limited FY 2005
funds were available for work on
proposed listing determinations for the
following candidate species included in
Table 1 of this notice: Arctic grayling,
Georgia pigtoe, interrupted rocksnail,
Astelia waialealae, Cyrtandra
kaulantha, and Phyllostegia hispida.
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FY 2005 LISTING ALLOCATION
Allocated
FY05 Appropriation (including space reprogramming) ............................................................................................
Space reprogramming (program’s portion of rent for building space) ....................................................................
Regional & Washington Offices (staff salaries & benefits) .....................................................................................
Printing .....................................................................................................................................................................
90-day findings ........................................................................................................................................................
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Sfmt 4702
E:\FR\FM\12SEP2.SGM
12SEP2
$5,604,178
254,749
1,344,660
612,405
613,224
Available
balance
$5,604,178
5,349,429
4,004,769
3,392,364
2,779,140
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FY 2005 LISTING ALLOCATION—Continued
Allocated
12-month findings ....................................................................................................................................................
Proposed Listing/CH ................................................................................................................................................
Final Listing/CH .......................................................................................................................................................
Attorney Fees/Litigation Expenses ..........................................................................................................................
Specific details regarding the
individual actions taken using the FY
2005 funding, which precluded our
ability to undertake listing proposals for
any of the candidate species, except the
species noted above, are provided below
(information on the cost of individual
actions is part of our administrative
record).
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. Until FY 2006, 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 (at least one staff person)
for listing actions (e.g., evaluating the
status of species to help ensure that a
emergency listing action can be taken if
necessary, and 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. This work includes providing
training and oversight of field personnel
and reviewing their work and making
recommendations to the Regional
Director on listing actions. Where this is
the case, there are no funds available for
high-priority listing actions.
The overall Listing Program situation
in FY 2006 is similar to that in FY 2005.
For FY 2006, Congress appropriated
$5,131,000 (after rescissions) to the
listing program for activities other than
critical habitat designations for already
1,342,159
579,370
550,116
307,400
Available
balance
1,436,981
857,611
307,495
95
listed species (Pub. L. 109–54, signed on
August 2, 2005). We have fully allocated
the $5,131,000 to fund the following
listing actions: Any emergency listings;
essential litigation-related,
administrative, and program
management functions; compliance
with court orders or court-approved
settlement agreements requiring petition
findings or listing determinations;
statutorily-required petition findings;
other high-priority listing actions; and
work on proposed listing
determinations for some high-priority
candidate species. In addition, by the
end of FY 2005 we had realized some
savings, largely in printing costs, as
compared to our estimated costs.
Therefore, we were able to reallocate
these remaining FY 2005 funds to help
cover some of the printing costs
associated with listing actions in FY
2006. As a result, The FY 2006 funds
needed for printing costs were reduced
and we are able to fund more work than
otherwise would have been possible
with only our FY 2006 listing budget.
FY 2006 LISTING ALLOCATION
Allocated
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FY06 Appropriation (including space reprogramming) ............................................................................................
Space reprogramming (program’s portion of rent for building space) ....................................................................
Regional & Washington Offices (staff salaries and benefits) ..................................................................................
Printing .....................................................................................................................................................................
90-day findings ........................................................................................................................................................
12-month findings ....................................................................................................................................................
Proposed Listing/CH ................................................................................................................................................
Final Listing/CH .......................................................................................................................................................
Attorney Fees/Litigation Expenses ..........................................................................................................................
For FY 2006 we have eliminated
capability funding, and instead have
allocated to the regions an amount
necessary to support a regional office
staff capable of supervising the
workload of packages in the region.
With respect to funds appropriated for
designation of critical habitat, the
majority of these funds in the critical
habitat subcap will be spent complying
with designating critical habitat under
court-order or court-approved
settlement agreements. We allocated a
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16:24 Sep 11, 2006
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small portion of the money not needed
to fund these critical habitat
designations for work on statutorilyrequired petition findings. While we
have more funds in FY 2006 (than in FY
2005) available for listing actions that
are not court-ordered or the subject of
court-approved settlement agreements,
we must use the majority of these funds
to work on or complete statutorilyrequired petition findings. During the
current fiscal year, we will issue
proposed listing rules for the highest
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Fmt 4701
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$5,130,594
261,817
1,610,150
33,000
508,796
1,350,653
813,460
452,718
100,000
Available \
balance
$5,130,594
4,868,777
3,258,627
3,225,627
2,716,831
1,366,178
552,718
100,000
0
priority candidate species only if doing
so does not jeopardize our ability to
comply with court orders, courtapproved settlement agreements, or
unqualified statutory deadlines. Thus,
as of the date of the publication of this
CNOR, we anticipate that we will have
only limited FY 2006 funds available to
work on proposals to list any of the
candidate species included in Table 1.
Consequently we continue to find that
proposals to list all of the petitioned
candidate species included in Table 1
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are warranted but precluded, except the
Arctic grayling, Georgia pigtoe,
interrupted rocksnail, Astelia
waialealae, Cyrtandra kaulantha, and
Phyllostegia hispida (which are being
funded this year). 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 2006 (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,
proposed rules 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 and remove qualified
species to the Lists. Our progress in FY
2005 includes work in the following
categories: (1) Preparation and
publication of final listing
determinations involving 6 species; (2)
preparation of final listing
determinations (not completed in FY
2005) for 13 species; (3) preparation of
proposed listing actions (not yet
completed so not yet published) for 8
species; and (4) listing petition findings
for 303 species (includes 10 completed,
33 not completed, and 260 resubmitted
findings). Specific information
regarding each of these categories for FY
2005 is provided below, followed by a
description of our anticipated FY 2006
progress.
FY 2005 (1) Final listing
determinations—We prepared and
published in the Federal Register final
listing determinations for six species, all
of which had absolute statutory
deadlines imposed by section 4(b)(6).
These included final regulations listing
the following species:
• Southwest Alaska distinct
population segment of the northern sea
otter (70 FR 46365; August 9, 2005;
LPN=3) (This final listing was not the
result of a deadline established by a
court order or a court-approved
settlement agreement. Rather, this was
the highest priority listing action for the
Alaska Region. The Alaska Region
generally has not faced the relatively
heavy Listing Program workload
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experienced by several other Regions,
and consequently was able to use their
limited Regional office capability
funding in FY 2005 to support the
completion of this 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).
• Koster’s springsnail, Roswell
springsnail, Noel’s amphipod, and
Pecos assiminea (70 FR 46303; August
9, 2005, LPN=2) (The work on the final
listing package that included these four
species was in response to a courtapproved settlement agreement as well
as having an absolute statutory
deadline).
• Salt Creek tiger beetle (70 FR 58335;
October 6, 2005; LPN=3) (The work on
this species was in response to a courtorder).
We note that the work on these
species, except the northern sea otter
and Salt Creek tiger beetle, included
funding for the designation of critical
habitat. 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 these four species. 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.
(2) We funded work on final listing
determinations for the Gila chub and 12
species of picture wing flies from
Hawaii for which work was not
completed in FY 2005. The work on
these species was also in response to
court-approved settlement agreements.
(3) We funded work on proposed
listing determinations for the following
species for which work was not
completed in FY 2005: Cowhead Lake
tui chub (reproposal), fluvial Arctic
grayling (distinct population segment of
the Upper Missouri River) (LPN=3) (the
work on this species was also in
response to a court-approved settlement
agreement), Georgia pigtoe (LPN=2),
interrupted rocksnail (LPN=2), Astelia
waialealae (LPN=2), Cyrtandra
kaulantha (LPN=2), Penstemon
grahamii (Graham’s beardtongue)
(LPN=2) (the work on this species was
also in response to a court-approved
settlement agreement), and Phyllostegia
hispida (LPN=2).
(4) We funded work on 300 petition
findings. This involved 90-day findings,
initial 12-month findings, and findings
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53773
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 was contrary
to our previous 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.
In FY 2005, we funded work on and
published petition findings for the
following 10 species: Pygmy rabbit (notsubstantial 90-day finding) (70 FR
29253; May 20, 2005), California spotted
owl (substantial 90-day finding) (70 FR
35607; June 21, 2005), boreal toad (notwarranted 12-month finding) (70 FR
56880; September 29, 2005), headwater
chub and Lower Colorado River Basin
population of the roundtail chub
(substantial 90-day finding) (70 FR
39981; July 12, 2005), American eel
(substantial 90-day finding) (70 FR
38849; July 6, 2005), 3 springsnails
(Jackson Lake, Harney Lake, and
Columbia) (substantial 90-day finding)
(70 FR 20515; April 20, 2005), and
Dalea tentaculoides (Gentry indigo
bush) (not-warranted 12-month finding)
(70 FR 56426; September 27, 2005). All
12-month findings have absolute
statutory deadlines. Because of Badgley,
all 90-day findings arguably also have
absolute statutory deadlines. In
addition, the work on all these species,
with the following exception, was in
response to court orders or courtapproved settlement agreements. The
American eel was the highest priority
listing action for the Northeast Region.
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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 2005 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.
The allocated funds also supported
work on petition findings that were not
completed in FY 2005 for the following
34 species (we worked on these petition
findings pursuant to a court order, a
court-approved settlement agreement, or
to meet statutory deadlines; those
marked with a ‘‘+’’ we worked on
pursuant to a court order/courtapproved settlement agreement, the
others (unmarked) we worked on to
meet statutory deadlines): Yellowstone
population of buffalo (90-day finding),
New England cottontail (warranted but
precluded 12-month finding—published
as part of this CNOR), Douglas County
subspecies of northern pocket gopher+
(90-day finding), Anacapa deer mouse
(90-day finding), American dipper+ (90day finding), long-tailed duck+ (90-day
finding), red knot (90-day finding),
yellow-billed loon+ (90-day finding),
southeastern snowy plover and
wintering population of piping plover
(90-day finding), cerulean warbler (12month finding), Mexican garter snake+
(90-day finding), northern water snake
(90-day finding), Berry Cave salamander
(90-day finding), American eel (12month finding), kokanee (90-day
finding), longnose sucker (90-day
finding), California golden trout (12month finding), Yellowstone cutthroat
trout+ (12-month finding) (we published
the opening of a comment period for a
12-month finding for this species on
September 1, 2005; 70 FR 52059), Black
Hills (Cooper’s Rocky) mountainsnail+
(90-day finding), Uinta mountainsnail+
(90-day finding), Cicurina cueva+ (12month finding) (we published two
notices to reopen the comment period
(on May 23, 2005, and August 16, 2005)
(70 FR 29471 and 70 FR 48093) in order
to provide the public an opportunity to
consider and comment on new
information we received after
publishing the 90-day finding for this
species), 4 subspecies of
Pseudocopacodes enus (12-month
finding), Andrew’s dune scarab beetle
(90-day finding), 3 invertebrates
(Stygobromus kenki, Stygobromus
phreaticus, and Acanthocyclops
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columbiensis—90-day finding),
Castanea ozarkensis (Ozark chinquapin)
(90-day finding), Gilia (=Alicellia)
tenuis (Mussentuchit gilia)+ (90-day
finding), Sidalcea hendersonii
(Henderson’s checkermallow) (90-day
finding), Usnea longissima (90-day
finding).
In addition, we completed some
initial and some resubmitted petition
findings required by statute for a total of
260 petitioned species that are
candidates. We published these findings
on May 11, 2005, as part of the previous
Candidate Notice of Review (CNOR) (70
FR 24870). Since we had identified the
majority 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 2006
includes work in the following
categories: (1) Work toward preparation
and publication of final listing actions
for 15 species; (2) work toward
preparation and publication of proposed
listing actions for 6 species; and (3)
work on petition findings for 72 species
that are not candidate species (we made
or are making these petition findings
pursuant to a court order, a courtapproved settlement agreement, or to
meet statutory deadlines), initial
petition findings for 2 species that are
also included in this notice as candidate
species, resubmitted petition findings
for 245 candidate and 5 listed species
that were petitioned prior to the last
CNOR, and revised 12-month petition
findings for 10 candidate species that
are we removing from candidate status
through this notice. Specific
information regarding each of these
categories for FY 2006 is provided
below. We note also that Regions will
continue to monitor the status of
candidates and prepare emergency
listing packages as needed.
FY 2006 (1) We funded work on the
final listing determinations for the
following species: Queen Charlotte
goshawk (remand of our previous listing
determination), Gila chub (70 FR 66663;
November 2, 2005, LPN=2), 12 species
of picture-wing flies from Hawaii (71 FR
26835; May 9, 2006) (prior to publishing
the final rule, we published a notice to
reopen the comment period on the
proposed listing rule; 70 FR 57851;
October 4, 2005), and Penstemon
grahamii (Graham’s beardtongue) (work
not yet completed). These final listing
determinations were in response to
court orders or court-approved
settlement agreements. Additionally,
since the Gila chub, 12 species of
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Fmt 4701
Sfmt 4702
picture-wing flies, and Graham’s
beardtongue were proposed for listing, a
final listing determination is subject to
an absolute statutory deadline.
(2) We funded listing determinations
for flat-tailed horned lizard (remand of
our withdrawal of a proposed rule to
list) (we published a withdrawal of the
proposed rule on June 28, 2006; 71 FR
36745)(we also had published notices to
reopen the comment period on our
reinstated proposed rule on March 2
and again on April 21, 2006; 71 FR
10631 and 71 FR 20637), fluvial Arctic
grayling (distinct population segment of
the Upper Missouri River) (LPN=3) (the
work on this species was also in
response to a court-approved settlement
agreement), Cowhead Lake tui chub
(reproposal), and Penstemon grahamii
(Graham’s beardtongue) (71 FR 3157;
January 19, 2006). We also funded work
on proposed listing proposals for the
following 5 high-priority candidate
species for which work was not
completed in FY 2006 prior to the
publication of this CNOR: Rough
hornsnail (LPN=2), black mudalia
(LPN=2), Georgia pigtoe (LPN=2),
interrupted rocksnail (LPN=2), Astelia
waialealae (LPN=2), Cyrtandra
kaulantha (LPN=2), and Phyllostegia
hispida (LPN=2).
(3) We funded work on and published
petition findings for the following
species (listing actions for species
marked with a ‘‘+’’ are per court order/
court-approved settlement agreement in
addition to having a statutory deadline):
Gunnison’s prairie dog+ (not-substantial
90-day finding) (71 FR 6241; February 7,
2006); Douglas County subspecies of the
northern pocket gopher+ (notsubstantial 90-day finding (71 FR 7715;
February 14, 2006); polar bear
(substantial 90-day finding) (71 FR
6745; January 9, 2006); Black Hills,
South Dakota, population of the
American dipper+ (not-substantial 90day finding) (71 FR 4341; January 26,
2006); Florida scrub-jay+ (notsubstantial 90-day petition findings on 2
petitions to reclassify as endangered)
(71 FR 4092; January 25, 2006);
Gunnison sage-grouse+ (not-warranted
12-month finding) (71 FR 19953; April
18, 2006); California spotted owl+ (not
warranted 12-month finding) (71 FR
298896; May 24, 2006) (we also
published a notice to reopen the
comment period on the 90-day petition
on October 14, 2005; 70 FR 60051);
northern Mexican gartersnake+
(substantial 90-day finding) (71 FR 315;
January 4, 2006); Siskiyou Mountains
and Scotts Bar salamanders+ (notsubstantial 90-day finding) (71 FR
23886; April 25, 2006); Distinct
Population Segment of the roundtail
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chub in the Lower Colorado River Basin
and the Headwater chub+ (notwarranted and warranted 12-month
findings) (71 FR 26007; May 3, 2006),
Yellowstone cutthroat trout+ (notwarranted 12-month finding) (71 FR
8818; February 21, 2006); Black Hills
(Cooper’s Rocky) mountainsnail+ (notsubstantial 90-day finding) (71 FR 9988;
February 28, 2006), Uinta
mountainsnail+ (not-substantial 90-day
finding) (70 FR 69303; November 15,
2005); Greater Adams cave beetle and
Lesser Adams cave beetle (notwarranted 12-month finding) (70 FR
72973; December 8, 2005); Casey’s June
beetle (substantial 90-day finding) (71
FR 44960; August 8, 2006); Andrews’
Dune scarab beetle (not-substantial 90day finding) (71 FR 26444 May 5, 2006);
island marble butterfly+ (substantial 90day finding) (71 FR 7497; February 13,
2006); Hermes copper butterfly (notsubstantial 90-day finding) (71 FR
44966; August 8, 2006); Sand Mountain
blue butterfly (substantial 90-day
finding) (FR 71 44988; August 8, 2006);
Thorne’s hairstreak butterfly (notsubstantial 90-day finding) (71 FR
44980; August 8, 2006); Cicurina cueva+
(not-warranted 12-month finding) (70
FR 75071; December 19, 2005); 16 insect
species from Algondones Dunes (notsubstantial 90-day finding) (71 FR
47765; August 18, 2006); Agave
eggersiana and Solanum conocarpum+
(not-warranted 12-month finding) (71
FR 11367; March 7, 2006); Gilia
(=Aliciella) tenuis+ (Mussentuchit gilia)
(not-substantial 90-day finding) (71 FR
4337; January 26, 2006); and Sidalcea
hendersonii (Henderson’s
checkermallow—not-substantial 90-day
finding) (71 FR 8252; February 16,
2006). We funded work on statutorilyrequired petition findings for the
following species (not yet completed so
not yet published): Polar bear (12-month
finding) (we reopened the comment
period on the status review for the 12month petition finding on May 17, 2006;
71 FR 28653) , Utah prairie dog (90-day
finding on reclassification to
endangered), black-footed albatross (90day finding), tricolored blackbird (90day finding), long-tailed duck+ (90-day
finding), southwestern population of
bald eagle (90-day finding), Columbian
sharp-tailed grouse (90-day finding),
yellow-billed loon+ (90-day finding),
Mono Basin population of greater sagegrouse (90-day finding), southeastern
snowy plover and wintering population
of piping plover (12-month finding),
cerulean warbler (12-month finding),
northern Mexican garter snake+ (12month finding), northern water snake
(12-month finding), Tucson shovel-
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Jkt 208001
nosed snake (90-day finding), Florida
population of gopher tortoise (90-day
finding), Berry Cave salamander (12month finding), Jollyville plateau
salamander (90-day finding), American
eel (12-month finding), San Felipe
gambusia (90-day finding), longnose
sucker (12-month finding), 3
springsnails (Jackson Lake, Harney
Lake, and Columbia) (12-month
finding), 3 invertebrates (Stygobromus
kenki, Stygobromus phreaticus, and
Acanthocyclops columbiensis) (12month finding), island marble butterfly+
(12-month finding), Mt. Charleston blue
butterfly (90-day finding), Astragalus
anserinus (Goose Creek milkvetch) (90day finding), Astragalus debequaeus
(DeBeque milkvetch) (90-day finding),
Castanea ozarkensis (Ozark chinquapin)
(90-day finding), Sclerocactus
brevispinus (Pariette cactus) (90-day
finding). We funded work on statutorilyrequired initial 12-month petition
findings for the New England cottontail
(substantial 90-day finding was
published on June 30, 2004) and red
knot (we also made the statutorilyrequired 90-day finding through this
CNOR), which are being published as
part of this CNOR (warranted but
precluded findings). We also funded
work on resubmitted petitions findings
for 245 candidate species and 5 listed
species (species petitioned prior to the
last CNOR). Note, we have not updated
our resubmitted petition findings for the
Columbia Basin population of the
greater sage-grouse or for the Missouri
River population of fluvial Arctic
grayling in this notice as we are
considering new information and will
update our findings at a later date. As
explained above, these resubmitted
petition findings are required by statute
and findings for these 245 candidates
and 5 listed species are being published
as part of this CNOR. We also funded
revised 12-month petition findings for
10 candidate species that we are
removing from candidate status, which
are being published as part of this
CNOR (see Summary of Candidate
Removals). 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
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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 2005 and FY
2006 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
high-priority Service-initiated listing
determinations, essential litigation
support, and administrative and
management tasks. We note that we are
not discussing specific actions we have
taken on progress towards removing
species from the lists of threatened or
endangered species in this notice since
that work is conducted with
appropriations to our Recovery program,
a separately-budgeted component of the
Endangered Species Program. However,
we do note that in FY 2005 we delisted
one species (Helianthus eggertii
(Eggert’s sunflower); 70 FR 48482;
August 18, 2005) and, to date in
FY2006, we have delisted two species
(the Arizona Distinct Population
Segment of the Cactus Ferruginous
Pygmy-owl; 71 FR 19452; April 14,
2006; and, Agave arizonica (Arizona
agave); 71 FR 35195; June 19, 2006).
The majority of the money to add
qualified species to the list is consumed
in complying with court orders or courtapproved settlement agreements
requiring petition findings or listing
determinations, and essential litigationrelated, administrative, and program
management functions related to these
findings and determinations (including
preparing and allocating budgets,
responding to Congressional and public
inquiries, public outreach, gathering
and assessing the scientific information
used as the basis for our listing
decisions, writing the document, and
reviewing those listing
recommendations made by our Field
and Regional Office staff). Therefore, 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,
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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.
Although we have not been able to
resolve the listing status of many of the
candidates, several programs in the
Service contribute to the conservation of
these species. In particular, we have a
separate budgeted program, the
Candidate Conservation program, which
focuses on providing technical expertise
for developing conservation strategies
and agreements to guide voluntary onthe-ground conservation work for
candidate and other at-risk species. The
main goal of this program is to address
the threats facing candidate species. If
sufficiently successful, this eliminates
the need to list them, allowing us to
remove them from the candidate list.
Through this program, we work with
our partners (other Federal agencies,
State agencies, Tribes, private
landowners, and private conservation
organizations) to address the threats to
candidate species and other species atrisk. We are actively engaged in the
conservation of these species and have
over 115 voluntary conservation
agreements that are being implemented
for 190 species covering 4.8 million
acres of habitat. For example, we are
currently implementing a Candidate
Conservation Agreement for the
Louisiana pine snake, a candidate
species. This agreement between the
Fish and Wildlife Service, U.S. Forest
Service, U.S. Department of Defense,
Texas Parks and Wildlife Department,
and Louisiana Department of Wildlife
and Fisheries was completed in 2003
and is designed to identify and establish
management for the Louisiana pine
snake on Federal lands in Texas and
Louisiana. The agreement provides a
means for all the partnering agencies to
work cooperatively on projects that
avoid and minimize impacts to the
snake. We also have provided funds
from the Endangered Species Private
Landowner Incentive Program and
Private Stewardship Grants to a private
landowner for habitat restoration and
prescribed burning at Louisiana pine
snake sites on their property. Several
other Service programs (e.g. Fisheries,
Partners for Fish and Wildlife, Refuge
Wildlife and Habitat Management, and
Federal Assistance) contribute to
candidate conservation.
Through sustained implementation of
strategically designed conservation
efforts, we are actively working to
conserve many candidate species. In
some instances, this culminates in
making listing unnecessary. In the past
two years, for example, we have
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obviated the need to list six species
through conservation efforts, including
four candidate species: The Greater and
Lesser Adams Cave beetles, Camp
Shelby burrowing crayfish, and
Holsinger’s cave beetle.
Findings for Petitioned Candidate
Species
For our revised 12-month petition
findings for species we are removing
from candidate status, see summaries
above under ‘‘Summary of Candidate
Removals.’’
Mammals
Pacific Sheath-tailed Bat, American
Samoa DPS (Emballonura semicaudata
semicaudata)—The following summary
is based on information contained in
our files. This small bat is a member of
the Emballonuridae, an Old World bat
family that has an extensive
distribution, primarily in the tropics.
The Pacific sheath-tailed bat was once
common and widespread in Polynesia
and Micronesia and it is the only
insectivorous bat recorded from a large
part of this area. The species as a whole
(E. semicaudata) occurred on several of
the Caroline Islands (Palau, Chuuk, and
Pohnpei), Samoa (Independent and
American), the Mariana Islands (Guam
and the CNMI), Tonga, Fiji, and
Vanuatu. While populations appear to
be healthy in some locations, mainly in
the Caroline Islands, they have declined
drastically in other areas, including
Independent and American Samoa, the
Mariana Islands, Fiji, and possibly
Tonga. Scientists recognize four
subspecies: E. s. rotensis, endemic to the
Mariana Islands (Guam and the
Commonwealth of the Northern Mariana
Islands (CNMI)); E. s. sulcata, occurring
in Chuuk and Pohnpei; E. s. palauensis,
found in Palau; and E. s. semicaudata,
occurring in American and Independent
Samoa, Tonga, Fiji, and Vanuatu. This
candidate assessment form addresses
the distinct population segment of E. s.
semicaudata that occurs in American
Samoa. E. s. semicaudata historically
occurred in American and Independent
Samoa, Tonga, Fiji, and Vanuatu. It is
extant in Fiji and Tonga, but may be
extirpated from Vanuatu and
Independent Samoa.
Current threats to this subspecies
include habitat loss, predation by
introduced species, small population
size, and disturbance to roosting caves.
The greatest threats at this time are
likely habitat loss and degradation, the
small numbers of bats detected in the
past two decades, and tropical storms.
Habitat loss and degradation and
predation by nonnative species are
believed to have been occurring for
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several decades. The Listing Priority
Number for E. s. semicaudata remains at
3 because the magnitude of the threats
is high, the threats are imminent, and
the taxon in question is a population of
a subspecies.
Pacific Sheath-tailed Bat
(Emballonura semicaudata rotensis),
Guam and the Commonwealth of the
Northern Mariana Islands—The
following summary is based on
information contained in our files. No
new information was provided in the
petition received on May 11, 2004. This
small bat is a member of the
Emballonuridae, an Old World bat
family that has an extensive
distribution, primarily in the tropics.
The Pacific sheath-tailed bat was once
common and widespread in Polynesia
and Micronesia and it is the only
insectivorous bat recorded from a large
part of this area. The species as a whole
(E. semicaudata) occurred on several of
the Caroline Islands (Palau, Chuuk, and
Pohnpei), Samoa (Independent and
American), the Mariana Islands (Guam
and the CNMI), Tonga, Fiji, and
Vanuatu. While populations appear to
be healthy in some locations, mainly in
the Caroline Islands, they have declined
drastically in other areas, including
Independent and American Samoa, the
Mariana Islands, Fiji, and possibly
Tonga. Scientists recognize four
subspecies: E. s. rotensis, endemic to the
Mariana Islands (Guam and the
Commonwealth of the Northern Mariana
Islands (CNMI)); E. s. sulcata, occurring
in Chuuk and Pohnpei; E. s. palauensis,
found in Palau; and E. s. semicaudata,
occurring in American and Independent
Samoa, Tonga, Fiji, and Vanuatu. This
candidate assessment form addresses
the Mariana Islands subspecies. E. s.
rotensis is historically known from the
Mariana Islands and formerly occurred
on Guam and in the CNMI on Rota,
Aguiguan, Tinian (known from
prehistoric records only), Saipan, and
possibly Anatahan and Maug. Currently,
E. s. rotensis appears to be extirpated
from all but one island in the Mariana
archipelago. The single remaining
population of this subspecies occurs on
Aguiguan, CNMI.
Threats to this subspecies have not
changed over the past year. The primary
threats to the subspecies include
predation by nonnative species, habitat
loss and degradation, small population
size, occurrence on one small island,
and disturbance to roosting caves.
Habitat loss and degradation (through
various means, but mainly by feral
ungulates at present) and predation by
nonnative species are believed to be
occurring now, and likely have been
occurring for several decades on
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Aguiguan and are, therefore, affecting
the entire remaining population of E. s.
rotensis. The subspecies may be near
the point where stochastic events, such
as typhoons, are increasingly likely to
affect its continued survival. The
disappearance of the remaining
population on Aguiguan would result in
the extinction of the subspecies. In
addition, scientists believe that a more
complete genetic examination of the
subspecies may result in its elevation to
a distinct species. The Listing Priority
Number for E. s. rotensis remains at 3
because the magnitude of the threats is
high, the threats are imminent, and the
taxon is question is a subspecies.
Cottontail, New England (Sylvilagus
transitionalis)—See above in ‘‘Summary
of New Candidates.’’ The above
summary is based on information in our
file and in the petition dated August 30,
2000.
Fisher, West Coast DPS (Martes
pennanti)—The following summary is
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. Native populations of fisher
currently occur in the North Coast
Ranges of California, the KlamathSiskiyou Mountains of northern
California and southern Oregon, and in
isolated populations occurring in the
southern Sierra Nevada in California.
Descendents of a fisher reintroduction
effort also occur in the southern Cascade
range in Oregon. There is a lack of
precise empirical data on West Coast
DPS fisher numbers. However, there is
a lack of detections over much of the
fisher’s historic range, even with
standardized survey and monitoring
efforts in California, Oregon and
Washington. There is also a high degree
of genetic relatedness within some
populations, and populations of native
fisher in California are separated by four
times the species’ maximum dispersal
distance. The above listed factors all
indicate that the likely extant fisher
populations are small and isolated from
one another.
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Major threats that fragment or remove
key elements of fisher habitat include
various forest vegetation management
practices such as timber harvest and
fuels reduction treatments. Other
potential major threats include: Standreplacing fire, Sudden Oak Death
Phytophthora, urban and rural
development, recreation development,
and highways. Major threats to fisher
that lead to direct mortality and injury
to fisher include; collisions with
vehicles, predation, and viral borne
diseases such as rabies, parvovirus,
canine distemper and Anaplasma
phagocytophilum. Existing regulatory
mechanisms on Federal, State and
private lands affect key elements of
fisher habitat and do not provide
sufficient certainty that conservation
efforts will be effective or will be
implemented. The magnitude of threats
is high as they occur across the range of
the DPS resulting in a negative impact
on fisher distribution and abundance.
However, the threats are non-imminent
as the greatest long-term risks to the
fisher in its west coast range are the
subsequent ramifications of the isolation
small populations, and the three
remaining areas containing fisher
populations appear to be stable or not
rapidly declining based on recent
survey and monitoring efforts. We
assigned this DPS a listing priority
number of 6 due to nonimminent threats
of a high magnitude.
Mazama pocket gopher (Thomomys
mazama (ssp. couchi, glacialis, louiei,
melanops, pugetensis, tacomensis,
tumuli, yelmensis)—The following
summary is based on information
contained in our files. No new
information was provided in the
petition received December 11, 2002.
These eight subspecies of pocket gopher
are associated with glacial outwash
prairies in western Washington. Of
these eight subspecies, six are likely still
extant (couchi, glacialis, melanops,
pugetensis, tumuli, and yelmensis). Few
of these glacial outwash prairies remain
in Washington today. Historically, such
prairies were only patchily distributed.
Now, residential and commercial
development, fire regime alteration, and
ingrowth of woody vegetation have
further reduced their numbers. In
addition, development in or adjacent to
these prairies has likely increased
predation on Mazama pocket gophers by
dogs and cats.
The magnitude of threat is high for
these subspecies due to their patchy and
isolated distribution, location in
habitats desirable for residential and
commercial development, threat of
invasive plants, and limited dispersal
capability of the species. Where human
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development occurs in proximity to
Mazama pocket gophers, predation by
domestic pets is an additional threat to
the species. The immediacy of threat is
imminent. Two of the subspecies (T. m.
louiei and T. m. tacomensis) are likely
extinct. Gravel pits threaten persistence
of one of the remaining subspecies (Roy
Prairie), and the populations of two
other subspecies (T. m. couchi and T. m.
yelmensis) are located on airports with
planned development. Yelm pocket
gophers (T. m. yelmensis) are also
threatened by other proposed
development on Fort Lewis. Thus we
assign a listing priority number of 3 to
these subspecies.
Palm Springs round-tailed ground
squirrel (Spermophilus tereticaudus
chlorus)—The following summary is
based on information in our files. No
new information was provided in the
petition received on May 11, 2004. The
range for the Palm Springs round-tailed
ground squirrel is generally described as
the Coachella Valley region that roughly
spans between San Gorgonio Pass and
the Salton Sea. A recent study
demonstrated that the primary habitat
for the Palm Springs round-tailed
ground squirrel in the Coachella Valley
is the mesquite sand dune/hummock
community. They are also found in
other low flat sandy areas or sand dunes
containing various types of desert shrub
communities, including creosote and
Atriplex ssp. Squirrels are also
occasionally found in fine sand
accumulated along banks, roads, and
among shrubs; as well as areas with
more coarse, hard-packed sand and
gravel.
Rapid growth of desert cities such as
Palm Springs and Palm Desert has
raised concerns about the conservation
of a squirrel restricted to the Coachella
Valley. Urban development and drops
in the groundwater table have
eliminated all but approximately 10
percent of Prosopis glandulosa var.
torreyana (mesquite) in the Valley; the
plant with which this squirrel is
strongly associated with. The mesquite
sand dune/hummock community is also
threatened by the decreasing water table
in the Coachella Valley. Mesquite is
phreatophytic, meaning that its roots are
adapted to grow deep into the water
table. Increasing water consumption
associated with growing urbanization is
lowering the water table below the level
at which mesquite roots can reach. No
formal protection is currently available
to this species in the majority of its
range. The California Environmental
Quality Act affords some indirect
protection to S. tereticaudus chlorus by
addressing impacts to other protected
species, most notably, the federally
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threatened Coachella Valley fringe-toed
lizard (Uma inornata). In 1993, the
Coachella Valley Association of
Governments initiated the Coachella
Valley Multiple Species Habitat
Conservation Plan (MSHCP) for the
Coachella Valley to address rare species
including S. tereticaudus chlorus.
However, this planning effort remains in
preparation and has not yet been
approved or implemented. Further, the
Coachella Valley MSHCP is proposing
to protect only 136 ha (336 acres) of
mesquite hummocks, which is only 35
percent of the remaining mesquite
hummocks left within the planning area
of the Coachella Valley MSHCP.
Mesquite hummocks near faults in the
Upper valley are not directly addressed
by the Coachella Valley Water District
Water Management Plan, and are
threatened by the planned and proposed
groundwater pumping for the rapidly
growing cities of Desert Hot Springs,
Cathedral City, and Indio.
We assigned the Palm Springs ground
squirrel subspecies a listing priority of
3 because the threats are ongoing and
are of a high magnitude. This roundtailed ground squirrel has lost
approximately 90 percent of its
preferred habitat, mesquite sand dune/
hummocks and suitable habitat in the
Coachella Valley has a high rate of
development.
Southern Idaho ground squirrel
(Spermophilus brunneus endemicus)—
The following summary is based on
information in our files. The southern
Idaho ground squirrel is endemic to four
counties in southwest Idaho; its total
known range is approximately 209,628
hectares (518,000 acres). Threats to
southern Idaho ground squirrels include
habitat deterioration and fragmentation,
direct killing from shooting, trapping or
poisoning, predation, competition with
Columbian ground squirrels, and
inadequacy of existing regulatory
mechanisms. Habitat deterioration and
fragmentation appear to be the primary
threats to the species. Nonnative
annuals now dominate much of this
species’ range, have changed the species
composition of vegetation, and have
altered the fire regime in a perpetuating
cycle throughout much of the range.
Habitat deterioration, destruction, and
fragmentation are thought to have
resulted in the current patchy
distribution of southern Idaho ground
squirrels. Based on recent genetic work,
southern Idaho ground squirrels are
subject to more genetic drift and
inbreeding than expected. Cost-effective
methods of habitat restoration are
currently unknown for southern Idaho
ground squirrels. Two Candidate
Conservation Agreements with
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Assurances (CCAAs) have been
completed for this species, both of
which allow agency access for
population and habitat surveys and
habitat enhancement/restoration work.
The magnitude of threat is low to
moderate for this species due to the two
CCAAs that have been completed, and
ongoing survey and habitat
enhancement/restoration efforts
conducted by other agencies. The
immediacy of the threat is imminent for
this species due to the prevalence and
dominance of nonnative vegetation and
the current patchy distribution of the
species. Thus, we assign a listing
priority number of 9 to this species.
Washington ground squirrel
(Spermophilus washingtoni)—The
following summary is based on
information contained in our files and
the petition received on March 2, 2000.
The Washington ground squirrel is one
of the smallest members of the subgenus
Spermophilus and is found within the
shrub-steppe habitat of the Columbia
Basin ecosystem of Oregon and
Washington. The soil types used by the
squirrels are distributed sporadically
within the species’ range, and have been
significantly fragmented by human
development in the Columbia Basin.
Approximately two-thirds of the
Washington ground squirrel’s total
historic range has been converted to
agriculture. When agriculture occurs,
little evidence of ground squirrel use
has been documented, and reports
indicate that agriculture (along with
other development) continues to
eliminate Washington ground squirrel
habitat in portions of its range.
Most remaining habitat is threatened
by the occurrence and spread of
nonnative species, particularly
cheatgrass. Nonnative plants threaten
squirrels by out-competing native
plants, thereby altering available cover,
food quantity and quality, and altering
fire intervals. The ultimate effects of
cheatgrass invasion on this species are
not fully understood. While Washington
ground squirrels eat cheatgrass, it is not
likely a viable long-term dietary option
since cheatgrass populations are
unstable during drought and contain
large amounts of indigestible silica
which may make it a poor nutrition
source. Fire recurrence intervals
typically switch from 20–100 years in
sagebrush-grassland ecosystems to 3–5
years in cheatgrass-dominant sites.
Increased fire occurrence reduces native
bunchgrass and shrub cover (by
competition or preventing the reestablishment of shrub cover) and
allows exotic species to further outcompete native species.
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The most contiguous, least-disturbed
expanse of suitable Washington ground
squirrel habitat within the species’
range occurs on the Boeing site and
Naval Weapons Training Facility near
Boardman, Oregon. In Washington, the
largest expanse of known suitable
habitat occurs on State and Federal
land. In Washington, recent declines in
some colonies have been precipitous for
unknown (possibly weather-related)
reasons. For example, in 2001 entire
colonies of ground squirrels were no
longer occupied on the Columbia
National Wildlife Refuge and Seep
Lakes Management Area near Othello,
Washington, despite protection for
species in this area. Recent surveys have
located additional sites in Washington
and Oregon. However, detections are
primarily located in the three disjunct
metapopulations, indicating
fragmentation and increased
vulnerability to natural and man-made
factors is still a widespread threat.
In Oregon, some threats are addressed
by the State listing of this species, and
by the recently signed Threemile
Canyon Farms Multi-Species Candidate
Conservation Agreement with
Assurances (Agreement). Participants in
the 25-year agreement include
Threemile Canyon Farms, The Nature
Conservancy, Portland General Electric
(PGE), the Oregon Department of Fish
and Wildlife (ODFW), and the Service.
Parties will implement habitat
management, operational modifications,
and conservation measures for four nonlisted species, including the Washington
ground squirrel. Under this agreement,
22,600 ac (9,145 ha) of the Boeing tract
was placed in a permanent ODFW
conservation easement (Boardman
Conservation Area) and 888 ac (356 ha)
of PGE property will be managed as part
of the BCA for the duration of the
Agreement.
Current threats to the long-term
persistence of this species include the
following: Historic and current habitat
loss from the conversion of habitat to
agriculture and other development,
habitat fragmentation, limited dispersal
corridors, recreational shooting, genetic
isolation and drift, spread of nonnative
species, and predation. Potential threats
include disease, drought, and possible
competition with related ground
squirrel species in disturbed habitat at
the periphery of their range. While there
are a variety of conservation actions and
research activities, they do not address
all of the threats throughout the species’
range. Due to the widespread current
and potential threats to the species we
conclude the magnitude of threats
remains high. Because the Agreement
addressed the imminent loss of a large
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portion of habitat to agriculture, and
because there are no other known, largescale efforts to convert suitable habitat
to agriculture, overall the threats are
nonimminent. We, therefore, kept the
listing priority number at 5.
Birds
Spotless crake, American Samoa DPS
(Porzana tabuensis)—The following
summary is based on information
contained in our files. No new
information was provided in the
petition received on May 11, 2004. P.
tabuensis is a small, dark, cryptic rail
found in wetlands and rank scrub or
forest in the Philippines, Australia, Fiji,
Tonga, Society Islands, Marquesas,
Independent Samoa, and American
Samoa (Ofu, Tau). The genus Porzana is
widespread in the Pacific, where it is
represented by numerous islandendemic and flightless species (many of
which are extinct as a result of
anthropogenic disturbances) as well as
several more cosmopolitan species,
including P. tabuensis. No subspecies of
P. tabuensis are recognized. The
American Samoa population is the only
population of spotless crakes under U.S.
jurisdiction. The available information
indicates that distinct populations of the
spotless crake, a species not noted for
long-distance dispersal, are definable.
The population of spotless crakes in
American Samoa is discrete in relation
to the remainder of the species as a
whole, which is distributed in widely
separated locations. Although the
spotless crake (and other rails) have
dispersed widely in the Pacific, island
rails have tended to reduce or lose their
power of flight over evolutionary time
and so become isolated (and vulnerable
to terrestrial predators such as rats). The
population of this species in American
Samoa is therefore distinct based on
geographic and distributional isolation
from spotless crake populations on
other islands in the oceanic Pacific, the
Philippines, and Australia. The
American Samoa population of the
spotless crake links the Central and
Eastern Pacific portions of the species’
range. The loss of this population could
cause an increase of roughly 500 miles
in the disjunction between the central
and eastern Polynesian portions of the
spotless crake’s range, and could result
in the isolation of the Marquesas and
Society Islands populations by further
limiting the potential for even rare
genetic exchange. Based on the
discreteness and significance of the
American Samoa population of the
spotless crake, we consider this
population to be a distinct vertebrate
population segment which warrants
review for listing under the Act.
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Threats to this species have not
changed over the past year. The
population in American Samoa is
threatened by small population size,
limited distribution, predation by
nonnative mammals, continued
development of wetland habitat, and
natural catastrophes such as hurricanes.
The co-occurrence of a known predator
of ground-nesting birds, the Norway rat,
and the only known population of the
spotless crake under U.S. jurisdiction,
along with the extremely restricted
observed distribution and low numbers,
indicate that the American Samoa
distinct population segment of this
species continues to merit status as a
candidate for listing. Based on our
assessment of existing information
about the imminence and high
magnitude of these threats, we assigned
the spotless crake a listing priority
number of 3.
Kauai creeper (Oreomystis bairdi)—
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
Kauai creeper is a small, insectivorous
forest bird that is found only on the
Hawaiian island of Kauai. It occurs in
mesic and wet montane forests at higher
elevations on the Alakai Plateau.
Surveys in 2000 showed that in the last
30 years the range of the Kauai creeper
has decreased from 88 to 36 square
kilometers (21,750 to 8,896 acres), that
the species has disappeared from much
of the periphery of its range, and that
the estimated population has declined
from 6,832 ± 966 to 1,472 ± 680 birds.
The creeper is primarily threatened by
diseases carried by nonnative
mosquitoes that occur over most or all
of its range. Experimental evidence has
shown that the malarial parasite does
not develop in birds below 13° Celsius
(C) (55° Fahrenheit (F)), and field
studies have found that maximum
malaria transmission occurs where
mean ambient summer temperature is
17 °C (63 °F). There are no forested areas
on Kauai where mean ambient
temperature is below 13 °C (55 °F),
meaning all areas are subject to malaria
at least periodically. Mosquitoes have
been found recently near the highest
elevations on Kauai. The disappearance
of the Kauai creeper from lowland
habitats indicates the species has not
evolved resistance to these diseases, and
it is very unlikely that such evolution
could occur rapidly enough to keep
pace with expansion of mosquito
populations. The creeper’s habitat is
being adversely affected by invasive
nonnative plants and by the browsing
and rooting of feral ungulates.
Nonnative plants displace native plant
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species required by the creeper, and
ungulates destroy the forest understory
and spread the seeds of nonnative
plants. Efforts are underway to control
nonnative plants in some areas, but over
most of the species range there is no
effective control of nonnative plants or
feral ungulates. Based on the imminent
threats of a high magnitude, we assigned
this species a listing priority number of
2.
Yellow-billed cuckoo, western U.S.
DPS (Coccyzus americanus)—The
following 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). The yellow-billed cuckoo is
a medium-sized bird of about 12 inches
(30 centimeters) in length with a
slender, long-tailed profile and a fairly
stout and slightly down-curved bill.
Plumage is grayish-brown above and
white below, with rufous primary flight
feathers with the tail feathers boldly
patterned with black and white below.
Western cuckoos breed in large blocks
of riparian habitats (particularly
woodlands with cottonwoods (Populus
fremontii) and willows (Salix sp.).
Dense understory foliage appears to be
an important factor in nest site
selection, while cottonwood trees are an
important foraging habitat in areas
where the species has been studied in
California. We consider the yellowbilled cuckoos that occur in the western
U.S. a distinct population segment
(DPS). The area for this DPS is west of
the crest of the Rocky Mountains.
The threats currently facing the
yellow-billed cuckoo include habitat
loss, cattle grazing, and pesticide
application. Principal causes of riparian
habitat losses are conversion to
agricultural and other uses, dams and
river flow management, stream
channelization and stabilization, and
livestock grazing. Available breeding
habitats for cuckoos have also been
substantially reduced in area and
quality by groundwater pumping and
the replacement of native riparian
habitats by invasive nonnative plants,
particularly tamarisk. Overuse by
livestock has been a major factor in the
degradation and modification of
riparian habitats in the western U.S. The
effects include changes in plant
community structure and species
composition and in relative abundance
of species and plant density. These
changes are often linked to more
widespread changes in watershed
hydrology. Livestock grazing in riparian
habitats typically results in reduction of
plant species diversity and density,
especially of palatable broadleaf plants
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like willows and cottonwood saplings,
and is one of the most common causes
of riparian degradation. In addition to
destruction and degradation of riparian
habitats, pesticides may affect cuckoo
populations. In areas where riparian
habitat borders agricultural lands, e.g.,
in California’s central valley, pesticide
use may indirectly affect cuckoos by
reducing prey numbers, or by poisoning
nestlings if sprayed directly in areas
where the birds are nesting. We retain
a listing priority number of 3 for the
yellow-billed cuckoo due to imminent
threats of a high magnitude.
Friendly ground-dove, American
Samoa DPS (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)—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.
Red knot (Calidris canutus rufa)—See
above in ‘‘Summary of New
Candidates.’’ The above summary is
based on information in our files and in
the petitions dated August 6, 2004, July
28, 2005, and August 2, 2005.
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
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
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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 retained a listing priority
number of 5 for this species.
Xantus’s murrelet (Synthliboramphus
hypoleucus)—The following summary is
based on information contained in our
files and the petition received on April
16, 2002. The Xantus’s murrelet is a
small seabird in the Alcid family that
occurs along the west coast of North
America in the U.S. and Mexico. The
species has a very limited breeding
distribution, only nesting on the
Channel Islands in southern California
and on islands off the west coast of Baja
California, Mexico. Nesting populations
in the U.S. and Mexico appear to have
declined due to a wide variety of
threats, with substantial declines
evident at some of the largest nesting
colonies and extirpations on three of the
seven Mexican islands. Some identified
threats include the possibility of oil
spills, reductions in prey availability,
introduced nonnative predators at
several nesting colonies, chronic human
disturbance, and artificial light
pollution. A dramatic decline (up to 70
percent) from 1977 to 1991 was detected
at the largest nesting colony in southern
California, possibly due to high levels of
predation on eggs by the endemic deer
mouse (Peromyscus maniculatus
elusus). Data on population trends from
other islands are scarce, particularly on
the Mexican nesting islands. Although
substantial declines in the Xantus’s
murrelet population appear to have
occurred over the last century, some of
the largest threats are being addressed,
and, to some degree, ameliorated in the
U.S.. Declines and extirpations of
Xantus’s murrelets at several nesting
colonies were thought to have been
caused by nonnative predators such as
rats (Rattus sp.) and feral cats (Felis
catus), which have been removed from
many of the islands where they once
occurred. Most notably, in 2002, rats
were eradicated from Anacapa Island in
southern California, which has resulted
in immediate improvements in
reproductive success at that island.
The Service has been working with
the State of California, National Park
Service, and National Oceanographic
and Atmospheric Administration
(NOAA Fisheries) to address the threats
of light pollution and human
disturbance. Many nocturnal seabirds
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are attracted to bright lights on
commercial fishing vessels. Xantus’s
murrelets and other seabirds become
exhausted by their continual attraction
and fluttering near lights or collide with
lighted vessels, the impact resulting in
injury or death. Chicks have been
known to become separated from their
parents due to vessel lights, and this
would have resulted in death of the
chicks because they are dependent on
their parents for survival. High-wattage
lights on commercial market squid
(Loligo opalescens) fishing vessels are
used at night to attract squid to the
surface of the water. These boats have
been reported operating in shallow
waters near Xantus’s murrelet nesting
colonies in the California Channel
Islands, with several vessels often
fishing simultaneously in the same area.
Unusually high predation on Xantus’s
murrelets by Western Gulls and Barn
Owls was reported at Santa Barbara
Island in 1999, and was attributed to
bright lights from the squid fishing that
occurred directly offshore for much of
the breeding season. To address this
threat, the California Fish and Game
Commission requires light shields and a
limit of 30,000 watts per boat, made
effective on May 31, 2000. The resulting
effects are still unknown.
The recent proposal to build a liquid
natural gas (LNG) facility 600 meters
(1,969 feet) off Islas Los Coronados in
Baja California, Mexico, is another
threat to the species. This island
contains one of the largest nesting
populations of Xantus’s murrelets in the
world. The construction and operation
of the proposed LNG facility at Islas Los
Coronados could increase human
disturbance to Xantus’s murrelets.
Potential 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. Due to the imminent
threats of high magnitude, we assigned
this species a listing priority number of
2.
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,
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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 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 individuals
and populations, necessary habitat
heterogeneity may be lost to large areas
of monoculture vegetation and/or
homogeneous 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 range of
the species. 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 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 is moderate, and
that the threats are ongoing and thus,
imminent. Consequently, a listing
priority number of 8 remains
appropriate for the species.
Greater sage-grouse, 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 May 4, 2004, notice, we found that
a listing proposal for this DPS was still
warranted but precluded by higher
priorities, and maintained its listing
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priority number of 6. The following
summary is based on information in our
files and a petition, dated May 14, 1999,
requesting the listing of the Washington
population of western sage grouse (C. u.
phaios). Currently, the American
Ornithologists’ Union recognizes two
subspecies of greater sage-grouse.
Compared to the eastern subspecies (C.
u. urophasianus), the western
subspecies has reduced white markings
and darker grayish-brown feathering,
resulting in a more dusky overall
appearance. Pursuant to Service policy
(61 FR 4722), on May 7, 2001, we
concluded that listing the Columbia
Basin DPS of western sage grouse,
which was historically found in
northern Oregon and central
Washington, was warranted, but
precluded by higher priority listing
actions (66 FR 22984). The Service
subsequently received two petitions
requesting the listing of the entire
ranges of the nominal western and
eastern subspecies of greater sagegrouse, dated January 24 and July 3,
2002, respectively. However, based on
communications with recognized
experts, disagreement as to the validity
of these subspecies designations exists.
When informed taxonomic opinion is
not unanimous, the Service must
evaluate the available information with
regard to our section 4 listing
responsibilities under the Endangered
Species Act (USFWS 1992). We
subsequently concluded that the
subspecies designations for greater sagegrouse are inappropriate given current
taxonomic standards (68 FR 6500 and
69 FR 933). In response to recent
judicial direction (Institute for Wildlife
Protection v. Norton (9th Cir. 2005,
Unpublished opinion)), we are in the
process of revisiting our current
interpretation of the taxonomic status of
the greater sage-grouse subspecies. We
will publish an updated finding
addressing the Columbia Basin DPS in
the Federal Register, either in the next
CNOR or in a separate notice, following
our judicially-directed reassessment of
the species’ taxonomy.
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 seabird that is found in several
areas of the subtropical Pacific and
Atlantic Oceans. In the Pacific, there are
three widely separated breeding
populations—one in Japan, one in
Hawaii, and one in the Galapagos.
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Populations in Japan and the Galapagos
are comparatively large and number in
the thousands, while the Hawaiian birds
represent a small, remnant population
of possibly only a few hundred pairs.
Band-rumped storm-petrels are most
commonly found in close proximity to
breeding islands. The three populations
in the Pacific are separated by long
distances across the ocean where birds
are not found. Extensive at-sea surveys
of the Pacific have revealed a broad gap
in distribution of the band-rumped
storm-petrel to the east and west of the
Hawaiian Islands, indicating the
distribution of birds in the central
Pacific around Hawaii is disjunct from
other nesting areas. The available
information indicates that distinct
populations of band-rumped stormpetrels are definable and that the
Hawaiian population is distinct based
on geographic and distributional
isolation from other band-rumped
storm-petrel populations in Japan, the
Galapagos, and the Atlantic Ocean. A
population also can be considered
discrete if it is delimited by
international boundaries across which
exist differences in management control
of the species. The Hawaiian population
of the band-rumped storm-petrel is the
only population within U.S. borders or
under U.S. jurisdiction. Loss of the
Hawaiian population would cause a
significant gap in the distribution of the
band-rumped storm-petrel in the
Pacific, and could result in the complete
isolation of the Galapagos and Japan
populations without even occasional
genetic exchanges.
The band-rumped storm-petrel
probably was common on all of the
main Hawaiian Islands when
Polynesians arrived about 1,500 years
ago, based on storm-petrel bones found
in middens on the island of Hawaii and
in excavation sites on Oahu and
Molokai. Nesting colonies of this
species in the Hawaiian Islands
currently are restricted to remote cliffs
on Kauai and Lehua Islet and highelevation lava fields on Hawaii.
Vocalizations of the species were heard
in Haleakala Crater on Maui in 1992, but
have not been detected there recently.
The significant reduction in numbers
and range of the band-rumped stormpetrel from prehistoric population levels
is due primarily to predation by humans
and nonnative predators introduced by
humans, including the domestic cat
(Felis catus), small Indian mongoose
(Herpestes auropunctatus), common
barn owl (Tyto alba), black rat (R.
rattus), Polynesian rat (Rattus exulans),
and Norway rat (R. norvegicus), which
occur throughout the main Hawaiian
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Islands, with the exception of the
mongoose, which is not established on
Kauai but may have an incipient
population there. Attraction of
fledglings to artificial lights and
collisions with artificial structures such
as communication towers and utility
lines are also a threat. Erosion of nest
sites caused by the actions of nonnative
ungulates and feral rabbits is a threat in
some locations. Efforts are underway in
some areas to reduce light pollution and
mitigate the threat of collisions, but
there are no large-scale efforts to control
nonnative predators in the Hawaiian
Islands. Based on the imminent threats
of a high magnitude, we assign this
distinct population segment a listing
priority number of 3.
Elfin woods warbler (Dendroica
angelae)—The following summary is
based on information contained in our
files. No new information was provided
in the petition received on May 11,
2004. The elfin woods warbler is a
small, entirely black and white warbler,
endemic to Puerto Rico. This species
was at first thought to occur only in the
high-elevation dwarf or elfin forests, but
it has since been found at lower
elevations, including shade coffee
plantations and secondary forests.
Dendroica angelae builds a compact cup
nest, usually close to the trunk and well
hidden among the epiphytes of a small
tree, and its breeding season extends
from March to June. This species forages
in the middle part of trees, gleaning
insects from leaves in the outer portion
of the tree crown. Dendroica angelae
has been documented from four
locations: Luquillo Mountains, Sierra de
Cayey, and the Commonwealth forests
of Maricao and Toro Negro. However, it
has not been recorded again in Toro
Negro and Cayey, following Hurricane
Hugo in 1989. Although there is no
estimate of total population of D
angelae, the latest estimate of 138 pairs
for the Luquillo Mountains suggests that
the total population may be less than
300 pairs.
Habitat destruction from expansion of
public facilities within the forests,
potential construction of additional
telecommunication towers and their
maintenance, disruption of breeding
activities from pedestrians and high
human use areas, switching from shade
to sun coffee plantations, timber
management practices, potential
predators, and catastrophic natural
events such as hurricanes and forest
fires threaten this species. Although
these threats are not imminent, because
most of the range of D. angelae is within
protected lands and there are no known
projects or management activities
planned that would result in mortality
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of this species, the magnitude of threat
to D. angelae is high, due to its
restricted distribution and low
population numbers. Therefore, we
assign a listing priority number of 5 to
this species.
Reptiles
Sand dune lizard (Sceloporus
arenicolus)—The following summary is
based on information contained in our
files and in the petition received June 6,
2002. The sand dune lizard is endemic
to a small area in southeastern New
Mexico (Chaves, Eddy, Lea, and
Roosevelt Counties) and adjacent west
Texas (Andrews, Crane, Ward, and
Winkler Counties). Within this area, the
known occupied and potentially
occupied habitat is only 1,697 square
kilometers (655 square miles) in New
Mexico and an area of unknown size in
west Texas. The sand dune lizard’s
distribution is localized and fragmented
(i.e., known populations are separated
by vast areas of unoccupied habitat),
and the species is restricted to sand
dune blowouts associated with active
sand dunes and shinnery oak (Quercus
harvardii) and scattered sandsage
(Artemisia filifolia) vegetation. Sand
dune lizards are not found at sites
lacking shinnery-oak dune habitat.
Extensive surveys within New
Mexico, conducted in conjunction with
a 5-year study, documented sand dune
lizards at only half of the sites surveyed.
Since February 2003, a Stakeholder
Group has met to create a conservation
strategy for the conservation of
shinnery-oak habitat that offers a range
of specific actions for the recovery of the
lesser prairie-chicken and sand dune
lizard and takes into account other uses
of the land. The group has broad
representation from the oil and gas and
livestock industries, conservation/
environmental interests, local
governments, sportsmen/recreation,
State and Federal agencies (New Mexico
State Land Office, New Mexico
Department of Agriculture, Natural
Resources Conservation Service, Fish
and Wildlife Service, and Bureau of
Land Management), and independent
technical advisors. The group
completed its Conservation Strategy that
outlines broad policies and plans for
land management and a set of voluntary
conservation efforts by stakeholders.
It is clear that shinnery-oak removal
(e.g., by treating with the herbicide
Tebuthiuron for livestock range
improvements) results in dramatic
reductions and extirpation of sand dune
lizards. Scientists repeatedly confirmed
the extirpation of sand dune lizards
from areas with herbicide treatment to
remove shinnery oak. In 1999, biologists
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estimated that about 25 percent of the
total sand-dune-lizard habitat in New
Mexico had been eliminated in the
previous 10 years. The population of
sand dune lizards has also been affected
by oil and gas field development. An
estimated 50-percent decline in sand
dune lizard populations can be expected
in areas with approximately 25 to 30 oil
and/or gas wells per section. The
distribution of sand dune lizards is
localized and fragmented, and this
species is a habitat specialist. Therefore,
impacts to its habitat will most likely
greatly decrease populations. If current
herbicide application continues and oil
and gas development progresses as
expected, the magnitude of threat to
sand dune lizards will increase.
Continued pressure to develop oil and
gas resources in areas with sand dune
lizards poses an imminent threat to the
species. Therefore, we continue to
assign this species a listing priority
number of 2.
Eastern massasauga (Sistrurus
catenatus catenatus)—The following
summary is based on information
contained in our files. No new
information was provided in the
petition received on May 11, 2004. The
eastern massasauga is one of three
recognized subspecies of massasauga. It
is a small, thick-bodied rattlesnake that
occupies shallow wetlands and adjacent
upland habitat in portions of Illinois,
Indiana, Iowa, Michigan, Minnesota,
Missouri, New York, Ohio,
Pennsylvania, Wisconsin, and Ontario.
Although the current range of S. c.
catenatus resembles the subspecies’
historical range, the geographic
distribution has been restricted by the
loss of the subspecies from much of the
area within the boundaries of that range.
Approximately 40 percent of the
counties that were historically occupied
by S. c. catenatus no longer support the
subspecies. S. c. catenatus is currently
considered imperiled in every State and
province in which 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 have a high
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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
the eastern massasauga subspecies.
Black pine snake (Pituophis
melanoleucus lodingi)—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.
Louisiana pine snake (Pituophis
ruthveni)—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 July 19, 2000.
Sonoyta mud turtle (Kinosternon
sonoriense longifemorale)—The
following summary is based on
information contained in our files. No
new information was provided in the
petition received on May 11, 2004. The
Sonoyta mud turtle occurs in a spring
and pond at Quitobaquito Springs on
Organ Pipe Cactus National Monument
in Arizona, and in the Rio Sonoyta and
Quitovac Spring of Sonora, Mexico.
Loss and degradation of stream habitat
from water diversion and groundwater
pumping, along with its very limited
distribution, is the primary threat to the
Sonoyta mud turtle. Sonoyta mud
turtles are highly aquatic and depend on
permanent water for survival. The area
of southwest Arizona and northern
Sonora where the Sonoyta mud turtle
occurs is one of the driest regions of the
southwest. Due to continuing 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
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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,
and northeastern and central Nevada,
but local populations within this entire
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 are 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 portion of 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. Despite the signing of
these two conservation agreements and
implementation of many actions in one
of them, population levels have not
increased significantly over levels that
were present at the time the agreements
were signed. There are several reasons
for this, including the fact that the
agreements do not cover entire range of
the species (Oregon and Idaho are not
included); the agreements mainly focus
on data collection and research to assess
current threats and distribution and
abundance, and important factors
affecting the populations are outside the
scope of the agreement/conservation
actions. Factors outside the agreements
are threats such as disease, winter kill,
and unexpected habitat degradation due
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to impacts of unauthorized livestock use
at a core population site of the species.
Also, implementation of one of the
agreements has been severely
constrained due to funding limitations
faced by the implementing agency.
Based on imminent threats of high
magnitude, we are continuing to assign
a listing priority number of 3 to this DPS
of the Columbia spotted frog.
Mountain yellow-legged frog, Sierra
Nevada DPS (Rana muscosa)—The
following summary is based on
information contained in our files and
the petition received on February 8,
2000. Also see our 12-month petition
finding published on January 16, 2003
(68 FR 2283). The mountain yellowlegged frog inhabits the high elevation
lakes, ponds, and streams in the Sierra
Nevada Mountains of California, from
near 4,500 feet (1,370 meters) to 12,000
feet (3,650 meters). The distribution of
the mountain yellow-legged frog is from
Butte and Plumas counties in the north
to Tulare and Inyo counties in the
south. A separate population in
southern California is already listed as
endangered (67 FR 44382).
Predation by introduced trout is the
best-documented cause of the decline of
the Sierra Nevada mountain yellowlegged frog, because it has been
repeatedly observed that nonnative
fishes and mountain yellow-legged frogs
rarely co-exist. Mountain yellow-legged
frogs and trout (native and nonnative)
do co-occur at some sites, but these cooccurrences probably are mountain
yellow-legged frog populations with
negative population growth rates in the
absence of immigration. To help reverse
the decline of the mountain yellowlegged frog, the Sequoia and Kings
Canyon National Parks have been
removing introduced trout since 2001.
Over 18,000 introduced trout have been
removed from 11 lakes since the project
started in 2001. The lakes are
completely-to-mostly fish-free and
substantial mountain yellow-legged frog
population increases have resulted. The
California Department of Fish and Game
(CDFG) has also removed or is in the
process of removing nonnative trout
from a total of between 10 and 20 water
bodies in the Inyo, Humboldt-Toiyabe,
Sierra, and El Dorado National Forests.
In the El Dorado National Forest, golden
trout were removed from Leland Lakes,
and attempts have been made to remove
trout from two sites near Gertrude Lake
and a tributary of Cole Creek; no data
showing increase in mountain yellowlegged frogs at these sites were
available.
In California, chytridiomycosis, more
commonly known as chytrid fungus, has
been detected in many amphibian
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species, including the mountain yellowlegged frog within the Sierra Nevada.
Recent research has shown that this
pathogenic fungus is widely distributed
throughout the Sierra Nevada, and that
infected mountain yellow-legged frogs
die soon after metamorphosis. Several
infected and uninfected populations
were monitored in Sequoia and Kings
Canyon National Parks over multiple
years, documenting dramatic declines
and extirpations in infected but not in
uninfected populations. In the summer
of 2005, 39 of 43 populations assayed in
Yosemite National Park were positive
for chytrid fungus.
The current distribution of the Sierra
Nevada mountain yellow-legged frog is
restricted primarily to publicly managed
lands at high elevations, including
streams, lakes, ponds, and meadow
wetlands located on national forests,
including wilderness and nonwilderness on the forests, and national
parks. In several areas where detailed
studies of the effects of chytrid fungus
on the mountain yellow-legged frog are
ongoing, substantial declines have been
observed over the past several years. For
example, in 2005 surveys in Yosemite
National Park mountain yellow-legged
frogs were not detectable at 37 percent
of 113 sites where they had been
observed in 2000 to 2002; in 2005 in
Sequoia and Kings Canyon National
Parks, mountain yellow-legged frogs
were not detected at 47 percent of sites
where they had been recorded 3 to 8
years earlier. A compounding effect of
disease-caused extinctions of mountain
yellow-legged frogs is that
recolonization may never occur, because
streams connecting extirpated sites to
extant populations now contain
introduced fishes, which act as barriers
to frog movement within
metapopulations. The listing priority for
the mountain yellow-legged frog in the
Sierra Nevada is highest for a
population and is a 3.
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 majority of the
remaining Oregon spotted frog
populations are small and isolated.
The threats to the species’ habitat
include development, livestock grazing,
introduction of nonnative plant species,
changes in hydrology due to
construction of dams and alterations to
seasonal flooding, and poor water
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quality. Additional threats to the species
are predation by nonnative fish and
introduced bullfrogs; competition with
bullfrogs for habitat; and diseases, such
as oomycete water mold Saprolegnia
and chytrid fungus infections. The
magnitude of threat is high for this
species because the small populations
with patchy and isolated distributions
are subject to a wide range of threats to
both individuals and their habitats that
could seriously reduce or eliminate any
of these isolated populations and further
reduce the range of the species. Habitat
restoration and management actions
have not prevented a decline in the
reproductive rates in some populations.
The threats are imminent because each
population is faced with multiple
ongoing and potential threats.
Therefore, we retained a listing priority
number of 2 for the Oregon spotted frog.
Relict leopard frog (Rana onca)—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 May 9, 2002.
Ozark hellbender (Cryptobranchus
alleganiensis bishopi)—The following
summary is based on information
contained in our files. No new
information was provided in the
petition received on May 11, 2004.
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 have increased, and present 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. In
2003, the Missouri Department of
Natural Resources added a 7-mile
stretch of the Jacks Fork River to the list
of impaired waters for organic wastes
(fecal coliform).
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
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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 waste being
generated 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 causes
of these trends are habitat destruction
and modification. Among these are
impoundment, channelization, and
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 the existence of
ongoing, high magnitude threats,
particularly the substantial increases in
recreational pressures on Ozark
hellbender rivers on an annual basis, we
assigned a listing priority number of 3
to the subspecies.
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
on a constant supply of clean water in
the Edwards Aquifer discharging from
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Barton Springs for its survival.
Urbanization dramatically alters the
normal hydrologic regime and water
quality of an area. Increased impervious
cover caused by development increases
the quantity and velocity of runoff that
leads to erosion and greater pollution
transport. Pollutants and contaminants
that enter the Edwards Acquifer are
discharged in salamander habitat at
Barton Springs and have 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
Edwards Aquifer can result in reduced
springflows that may also detrimentally
impact the salamander. The Texas
Commission on Environmental Quality
adopted the Edwards Rules in 1995 and
1997, which require a number of water
quality protection measures for new
development occurring in the recharge
and contributing zones of the Edwards
Aquifer. However, Chapter 245 of the
Texas Local Government Code permits
‘‘grandfathering’’ of state regulations.
Grandfathering allows developments to
be exempted from any new local or state
requirements for water quality controls
and impervious cover limits if the
developments were planned prior to the
implementation of such regulations. As
a result of the grandfathering law, very
few developments have followed these
ordinances. New developments are still
obligated to comply with regulations
that were applicable at the time when
project applications for development
were first filed. In addition, it is
significant that even if they were
followed with every new development,
these ordinances do not span the entire
watershed for Barton Springs.
Consequently, development occurring
outside these jurisdictions can have
negative consequences on water quality
and thus impact the species. Despite
having the Edwards Rules in place and
the existence of other local ordinances,
10 years of trend data continues to show
that water quality at Barton Springs is
declining. Because of the limited
distribution of this species, the
magnitude of the threats facing it is
high. We also consider the threats to be
imminent because urbanization is
ongoing and continues to expand over
the Barton Springs Segment of the
Edwards Aquifer and water quality
continues to degrade. Thus, we retained
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
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petition received on May 11, 2004. The
Georgetown salamander is know from
spring outlets along five tributaries to
the San Gabriel River and one cave in
the City of Georgetown, Williamson
County, Texas. The Georgetown
salamander has a very limited
distribution and depends on a constant
supply of clean water from the Northern
Segment of the Edwards Aquifer for its
survival.
Primary threats to this species are
degradation of water quality and
quantity due to expanding urbanization.
Increased impervious cover by
development increases the quantity and
velocity of runoff that leads to erosion
and greater pollution transport.
Pollutants and contaminants that enter
the Edwards Aquifer are discharged
from spring outlets in salamander
habitat and have serious morphological
and physiological effects to the species.
As the human population increases in
central Texas, greater demand on
groundwater sources occurs. Increased
pumping of the Edwards Aquifer results
in reduced springflows that may also
detrimentally impact the salamander.
The information regarding the
Edwards Rules described above in
relation to the Austin blind salamander
also applies to the Georgetown
salamander and is incorporated here by
reference. Because of the limited
distribution of the Georgetown
salamander, the magnitude of the
threats facing it is high. The threats are
also imminent because urbanization is
ongoing and continues to expand over
the Northern Segment of the Edwards
Aquifer. Thus, we retained a listing
priority number 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 increase threats of
contamination from spills, higher levels
of impervious cover, and subsequent
impacts to groundwater. Several
groundwater contamination incidents
have occurred within Salado
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salamander habitat. The Salado
salamander depends on a constant
supply of clean water from the Northern
Segment of the Edwards Aquifer for its
survival. Pollutants and contaminants
that enter the Edwards Aquifer
discharge in salamander habitat and
have 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 Edwards Aquifer can
result in reduced springflows that may
also detrimentally impact the
salamander.
Controls of nonpoint source pollution
in the watershed are implemented
through the Edwards Rules (water
quality protection measures for the
recharge and contributing zones of the
Edwards Aquifer) adopted by the Texas
Commission on Environmental Quality
(TCEQ) in 1995 and 1997. Although
implementation of the Edwards Rules in
other areas of the Northern Segment of
the Edwards Aquifer may have the
potential to affect conditions at spring
sites occupied by the Salado
salamander, the jurisdiction of TCEQ
does not extend into Bell County. For
this reason, compliance with the
Edwards Rules is not required in this
part of the Edwards Aquifer. There are
no other local or regional water
protection measures that have been put
in place for areas that feed the springs
known to be occupied by the Salado
salamander. Because of the limited
distribution of this species, the
magnitude of the threats facing it is
high. We also consider the threats to be
imminent because urbanization is
ongoing and contamination events are
occurring near spring sites known to
support Salado salamanders. Thus, we
retained a listing priority number of 2
for this species.
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). Yosemite toads are moderately
sized toads with females having black
spots edged with white or cream that are
set against a grey, tan or brown
background. Males have a nearly
uniform coloration of yellow-green to
olive drab to greenish brown. Yosemite
toads are most likely to be found in
areas with thick meadow vegetation or
patches of low willows near or in water,
and use rodent burrows for
overwintering and temporary refuge
during the summer. Breeding habitat
includes the edges of wet meadows,
slow flowing streams, shallow ponds
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and shallow areas of lakes. The historic
range of Yosemite toads in the Sierra
Nevada occurs from the Blue Lakes
region north of Ebbetts Pass (Alpine
County) to south of Kaiser Pass in the
Evolution Lake/Darwin Canyon area
(Fresno County). The historic
elevational range of Yosemite toads is
1,460 to 3,630 meters (4,790 to 11,910
feet).
The threats facing the Yosemite toad
include cattle grazing, timber
harvesting, recreation, disease, and
climate change. Inappropriate grazing
has shown to cause loss in vegetative
cover and destroying peat layers in
meadows, which lowers the
groundwater table and summer flows.
This may increase the stranding and
mortality of tadpoles, or make these
areas completely unsuitable for
Yosemite toads. Grazing can also
degrade or destroy moist upland areas
used as non-breeding habitat by
Yosemite toads and collapse rodent
burrows used by Yosemite toads as
cover and hibernation sites. Timber
harvesting and associated road
development could severely alter the
terrestrial environment and result in the
reduction and occasional extirpation of
amphibian populations in the Sierra
Nevada. These habitat gaps may act as
dispersal barriers and contribute to the
fragmentation of Yosemite toad habitat
and populations. Trails (foot, horse,
bicycle, or off-highway motor vehicle)
compact soil in riparian habitat, which
increases erosion, displaces vegetation,
and can lower the water table.
Trampling or the collapsing of rodent
burrows by recreationists, pets, and
vehicles could lead to direct mortality of
all life stages of the Yosemite toad and
disrupt their behavior. Various diseases
have been confirmed in Yosemite toads.
Mass die-offs of amphibians have been
attributed to: Chytrid fungal infections
of metamorphs and adults; Saprolegnia
fungal infections of eggs; iridovirus
infection of larvae, metamorphs, or
adults; and bacterial infections.
Yosemite toads probably are exposed to
a variety of pesticides and other
chemicals throughout their range.
Environmental contaminants could
negatively affect the species by causing
direct mortality; suppressing the
immune system; disrupting breeding
behavior, fertilization, growth or
development of young; and disrupting
the ability to avoid predation. We
retained a listing priority number of 11
for the Yosemite toad since the threats
are of moderate to low magnitude and
the threats are nonimminent at this
time.
Black Warrior waterdog (Necturus
alabamensis)—The following summary
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is based on information contained in
our files. No new information was
provided in the petition received on
May 11, 2004. 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 since little
attention was given to this species
between its description in 1937 and the
1980’s. There are a total of only 11
known historical records from 4
Alabama counties. Two of these sites
have now been inundated by
impoundments. Extensive survey work
was conducted in the 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. The North River,
Locust Fork, and Mulberry Fork, all
streams that this species inhabits are all
on the Environmental Protection
Agency’s list of impaired waters. An
additional threat to the Black Warrior
waterdog is the creation of large
impoundments that have flooded
thousands of square hectares (acres) of
its habitat. These impoundments are
likely marginal or unsuitable habitat for
the salamander. Due to the continuing,
imminent, high magnitude of the
pervasive water quality degradation in
the Black Warrior Basin, we assigned a
listing priority number of 2 to this
species.
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 small fish in the
perch family native to portions of the
Arkansas River basin. The species’ range
includes sites in extreme northwestern
Arkansas, southwestern Missouri, and
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northeastern Oklahoma. It also occurs in
a number of watersheds and isolated
streams in eastern Colorado, southcentral and southwestern Kansas, and in
the Cimarron watershed in northwest
Oklahoma. The species is most often
found in small spring-fed streams with
sand substrate and aquatic vegetation. It
appears stable at most sites where
spring flows persist. It has declined in
areas where spring flows have decreased
or been eliminated. We estimate that
currently there are approximately 145
locality occurrences of the Arkansas
darter distributed across the 5 States.
However, status information from much
of the Arkansas darter’s range is dated,
and new surveys are needed; some
survey work is being conducted in 2006.
Major threats to the species include
stream dewatering resulting from
groundwater pumping in the western
portion of the species’ range, and
development pressures in portions of its
eastern range. Spills and runoff from
confined animal feeding operations also
threaten the species locally throughout
its range. We have retained a listing
priority number of 11 for this species
based on nonimminent threats of a
moderate magnitude.
Cumberland darter (Etheostoma
susanae)—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.
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
requirements or natural history of the
Pearl darter. Pearl darters have been
collected from rivers and streams with
a variety of attributes, but are mainly
found over a gravel bottom substrate.
This species is historically known only
from localized sites within the
Pascagoula and Pearl River drainages in
Louisiana and Mississippi. Currently,
the Pearl darter is considered extirpated
from the Pearl River drainage and rare
in the Pascagoula River drainage. Since
1983, the range of the Pearl darter has
decreased by 55 percent. Pearl darters
are vulnerable to the cumulative
impacts of a variety of non-point
pollution types, such as sedimentation
and chemical, and also to more
localized and concentrated pollution
events. The steady yet gradual change in
river and tributary geomorphology and
hydrology over time is believed to
impact this species. Efforts are
underway to improve habitat by
reducing these threats and to increase
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and augment the numbers of Pearl
darters through husbandry efforts. The
magnitude of threat to this species is
high due to the species limited and
disjunct populations and threat due to
high vulnerability to sedimentation.
However, this threat is nonimminent
since no known projects are planned
directly affecting the species and the
decline of water quality is slow and
gradual. Therefore, we assigned this
species a listing priority number of 5.
Rush darter (Etheostoma
phytophilum)—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.
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 four
headwater tributaries of the Little Red
River. Factors affecting the remaining
populations include loss of suitable
breeding habitat, habitat and water
quality degradation, population
isolation, and severe population
declines exacerbated by stochastic
drought conditions. It is vulnerable to
alterations in physical habitat
characteristics such as the
impoundment of Greers Ferry Reservoir,
channel maintenance in the Archey
Fork, increased sedimentation from
eroding stream banks and poor riparian
management, and illegal gravel mining.
A 2004–2005 threats assessment by
Service personnel documented
occurrences of eroding stream banks,
poor riparian management, and illegal
gravel mining, and found 52 sites of
these activities on the Middle Fork, 28
sites on the South Fork, 8 sites on
Archey Fork, and 1 site in the Turkey/
Beech/Devils Fork system that are
potential contributors to the decline of
the species. The Middle Fork 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; 10,300 in 2000) of this
fish in the remaining populations and
continuing range restriction within the
tributaries (130.4 to 65.0 stream km).
According to a 2000 status survey,
yellowcheek darter numbers had
declined over a 20-year period by 83
percent in both the Middle Fork and
South Fork, and 60 percent in the
Archey Fork. No yellowcheek darters
were found in the Turkey Fork between
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1999 and 2005; the species has
apparently been extirpated in that reach.
Due to imminent threats of a high
magnitude that are not currently
targeted by conservation actions, we
assigned this species a listing priority
number of 2.
Fluvial arctic grayling, upper
Missouri River DPS (Thymallus
arcticus)—We have not updated our
finding with regard to fluvial arctic
grayling DPS in this notice. We received
a petition to list this species on October
2, 1992, and published our 12-month
finding on July 25, 1994 (59 FR 37738).
In the 2004 CNOR (70 FR 24870), we
found that a listing proposal for this
species was still warranted but
precluded by higher priorities, with a
listing priority number of 3. We are in
the process of considering new
information and conducting additional
evaluations regarding the fluvial arctic
grayling. Upon completion, we intend to
publish a listing determination for this
DPS species in the Federal Register.
Chucky madtom (Noturus
crypticus)—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 catfish known
from only 15 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 14
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.
Threats to the chucky madtom
include both extrinsic and intrinsic
factors. Extrinsic factors include
potential degradation of water quality
and breeding and sheltering habitat due
primarily to agricultural landuse
practices and secondarily to urban and
rural development in the watersheds of
Little Chucky and Dunn creeks. The
Service believes that intrinsic factors
including the potential demographic
effects of inbreeding, limited species
distribution, presumed low number of
individuals, and presumed low
fecundity and short life span
characteristic of closely related madtom
species pose imminent threats of a high
magnitude to the chucky madtom in its
only known extant and historic
locations. Therefore, we assigned the
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chucky madtom a listing priority
number of 2.
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 restricted to two karst
areas (limestone regions characterized
by sink holes, abrupt ridges, caves, and
underground streams), the Central
Perryville Karst and Mystery-Rimstone
Karst in Perry County, southeast
Missouri. Grotto sculpins have been
documented in only 5 caves. The
current overall range of the grotto
sculpin has been estimated to
encompass approximately 260 square
kilometers (100 square miles).
The small population size and
endemism of the grotto sculpin make it
vulnerable to extinction due to genetic
drift, inbreeding depression, and
random or chance changes to the
environment. The species’ karst habitat
is located down-gradient of the city of
Perryville, Missouri, which poses a
potential threat if contaminants from
this urban area enter cave streams
occupied by grotto sculpins. Various
agricultural chemicals, such as
ammonia, nitrite/nitrate, chloride, and
potassium have been detected at levels
high enough to be detrimental to aquatic
life within the Perryville Karst area.
More than half of the sinkholes in Perry
County contain anthropogenic refuse,
ranging from household cleansers and
sewage to used pesticide and herbicide
containers. As a result, potential water
contamination from various sources of
point and non-point pollution poses a
significant threat to the grotto sculpin.
Of the 5 cave systems documented to
have grotto sculpins, populations in one
cave system were likely eliminated,
presumably as the result of point-source
pollution. When the cave was searched
in the spring of 2000, a mass mortality
of grotto sculpin was noted, and
subsequent visits to the cave have failed
to document a single live grotto sculpin.
Thus, the species appears to have
suffered a 20-percent decrease in the
number of populations from the single
event. Predatory fish such as common
carp, fat-head minnow, yellow bullhead,
green sunfish, bluegill, and channel
catfish occur in all of the caves
occupied by grotto sculpin. These
potential predators may escape surface
farm ponds that unexpectedly drain
through sinkholes into the underground
cave systems and enter grotto sculpin
habitat. No regulatory mechanisms are
in place that would provide protection
to the grotto sculpin. Current threats to
the habitat of the grotto sculpin may
exacerbate potential problems
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associated with its low population
numbers and increase the likelihood of
extinction. Due to the high magnitude of
ongoing threats we assigned this species
a listing priority number of 2.
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. It has
also been found in the Wichita River
(within the Red River Basin), where it
may have once naturally occurred but
has since been extirpated. Current
information indicates that the
population within the 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 68 percent of its
historical range.
The most significant threat to the
existence of the sharpnose shiner is
potential reservoir development within
its current range. Additional threats
include irrigation and water diversion,
sedimentation, industrial and municipal
discharges, agricultural activities, instream sand and gravel mining, and the
spread of invasive saltcedar. The current
limited distribution of the sharpnose
shiner within the Upper Brazos River
Basin makes it vulnerable to
catastrophic events such as the
introduction of competitive species or
prolonged drought. The magnitude of
threat is high since the major threat of
reservoir development within the
current range of the species may render
its remaining habitat unsuitable. The
immediacy of threat is nonimminent
due to major reservoir projects not likely
occurring in the near future and the
potential implementation of other water
supply options that could preclude
reservoir development. For these
reasons, we assigned a listing priority
number of 5 to 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
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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 54 percent
of its historical range.
The most significant threat to the
existence of the smalleye shiner is
potential reservoir development within
its current range. Additional threats
include irrigation and water diversion,
sedimentation, industrial and municipal
discharges, agricultural activities, instream sand and gravel mining, and the
spread of invasive saltcedar. The current
limited distribution of the smalleye
shiner within the Upper Brazos River
Basin makes it vulnerable to
catastrophic events such as the
introduction of competitive species or
prolonged drought. The magnitude of
threat is high since the major threat of
reservoir development within the
current range of the species may render
its remaining habitat unsuitable. The
immediacy of threat is nonimminent
due to major reservoir projects not likely
occurring in the near future and the
potential implementation of other water
supply options that could preclude
reservoir development. For these
reasons, we assigned a listing priority
number of 5 to this species.
Zuni bluehead sucker (Catostomus
discobolus yarrowi)—The following
summary is based on information
contained in our files. No new
information was provided in the
petition 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, raising livestock, and
irrigation. Diverting water for
agricultural use is the primary purpose
of at least five impoundments, and
several other reservoirs act as floodcontrol structures. Degradation of the
upper watershed has led to increased
sedimentation, and many of the
reservoirs are now only shallow,
eutrophic (low oxygen) 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
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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 has been
the lead agency to develop a
conservation plan for Zuni bluehead
sucker. A study funded through section
6 of the Act was initiated in 2000, and
continued through 2005. The grant
included 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. The Zuni Bluehead Sucker
Recovery Plan was approved by the
New Mexico State Game Commission
during a State Game Commission on
December 15, 2004. The Recovery Plan
recommends preservation and
enhancement of extant populations and
restoration of historical Zuni bluehead
sucker populations. The recovery
actions prescribed by the State Recovery
Plan that we believe will reduce and
remove threats to this subspecies, will
require further discussions and
authorizations before they can be
implemented. Still, because of the
ongoing threats of high magnitude,
including loss of habitat, degradation of
remaining habitat, and others (i.e.,
drought and fire), we maintained the
current listing priority number of 3 for
this subspecies.
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. The
Texas hornshell is a freshwater mussel
found in the Black River of New Mexico
and one confirmed locality in the
mainstem Rio Grande of Texas and
Mexico. The primary threats are habitat
alterations such as stream bank
channelization, impoundments, and
diversions for agriculture and flood
control; contamination of water by the
oil and gas industry; alterations in the
natural riverine hydrology; and
increased sedimentation from prolonged
overgrazing and loss of native
vegetation. Riverine habitats in both the
Black River and the Rio Grande are
under constant threats from these
adverse changes. The magnitude of
threats is high because of the existence
of only one confirmed location in New
Mexico and Texas each, which makes
this species highly vulnerable to
extinction. The threats are imminent
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because past alterations to riverine
habitats have already occurred that
resulted in the much reduced
distribution of this species and demands
for water from the Rio Grande continue
to increase and make future habitat
degradation likely. Thus, we maintained
the listing priority number of 2 for this
species.
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. The threats are high
in magnitude since all populations of
this species are potentially threatened
by impoundments, sedimentation, small
population size, isolation of
populations, gravel mining, municipal
pollutants, agricultural run-off, nutrient
enrichment, and coal processing
pollution. However, the threats are
nonimminent at this time, and therefore,
we retained 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 62 percent (835 river
miles) of its range, most of which 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 populations.
Significant portions of the historic
range have been inundated by the
construction of at least 11 dams.
Channel instability downstream of these
dams has further reduced suitable
habitat and mussel distribution. Range
restriction and population declines have
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occurred due to habitat degradation
attributed to impoundments, mining,
sedimentation, and agricultural
pollutants. Rapid development and
urbanization in the Illinois River
watershed will likely continue to
increase sedimentation and
eutrophication to this river but
populations are currently stable in this
river. The remaining extant populations
are vulnerable to random catastrophic
events (e.g., flood scour, drought, toxic
spills), land use changes within the
limited range, and genetic isolation and
the deleterious effects of inbreeding.
These threats have led to the species
being intrinsically vulnerable to
extirpation. Although State regulations
limit harvest of this species, there is
little protection for habitat. The threats
are high in magnitude, as they occur
throughout the range of this species.
While some of the threats are ongoing
and thus, imminent, others are
nonimminent, but on the balance are
nonimminent. Thus, we assigned a
listing priority number of 5 to 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. One of
these has declined significantly over the
past few years, apparently due to
increased sedimentation at this location
and possibly other forms of non-point
source (NPS) pollution. The other two
populations appear to be small, but
relatively stable and recruiting. We
assigned the Alabama pearlshell a
listing priority of 2 due to the
vulnerability of small stream habitat to
continuing NPS pollution and the
decline of one of three known
populations.
Slabside pearlymussel (Lexingtonia
dolabelloides)—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.
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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 10 isolated stream segments.
Current status information for most of
the nine populations deemed to be
extant is available from recent periodic
sampling efforts (sometimes annually)
and other field studies. Comprehensive
surveys have taken place in the Middle
and North Forks Holston River, Paint
Rock River, and Duck River in the past
several years. Based on recent
information, the overall population of
the slabside pearlymussel is declining
rangewide and the species remains in
good numbers and is clearly viable in
just four streams. Two of the four largest
populations have undergone recent
declines (i.e., Middle and upper North
Fork Holston Rivers) and most of the
other populations are of doubtful
viability for the long term. Since the
nine remaining populations of the
slabside pearlymussel face potential
threats from impoundments,
sedimentation, small population size,
isolation of populations, gravel mining,
municipal pollutants, agricultural runoff, nutrient enrichment, and coal
processing pollution, the threats are
high in magnitude but are
nonimminent. Thus, we continue to
assign a listing priority number of 5 to
this mussel.
Georgia pigtoe (Pleurobema
hanleyanum)—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 pigtoe was
historically found in shallow runs and
riffles in large creeks and rivers of the
Coosa River drainage of Alabama,
Georgia, and Tennessee. The species is
currently known from localized portions
of the upper Conasauga River in Murray
and Whitfield Counties, Georgia. In
2005, the Coosa River in Cherokee
County, Alabama, was removed as
‘‘Current Range,’’ due to a lack of
documentation that the species
continues to exist at that locality. 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;
pollution remains an ongoing threat. We
assigned the Georgia pigtoe a listing
priority of 2 due to its restricted range
and continued lack of success in
locating living animals.
Altamaha spinymussel (Elliptio
spinosa)—See above in ‘‘Summary of
Listing Priority Changes in Candidates.’’
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The above summary is based on
information contained in our files. No
new information was provided in the
petition received on May 11, 2004.
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
restricted range of this snail, the
proximity to an expanding residential
area, and impacts from relatively heavy
recreational use, makes it vulnerable to
extirpation from stochastic or humancaused events. Threats to the colony
have not substantially changed or
increased over the past year. Recent
molecular phylogenic studies are
expected to clarify the level of
uniqueness of this taxon. With the
threats continuing at a moderate to low
and imminent level, we retained a
listing priority number of 9 for this
subspecies.
Bonneville pondsnail (Stagnicola
bonnevillensis)—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
fat-whorled pondsnail, also known as
the Bonneville pondsnail, occupies four
spring pools north of the Great Salt Lake
in Box Elder County, Utah. While the
number of individuals is unknown, the
total known occupied habitat is less
than one hectare. As a result of the
implementation of a Conservation
Agreement and Strategy, surveys are
being conducted to determine if other
populations are present. Previous and
ongoing threats include chemical
contamination of the groundwater.
Significant actions are underway to
remediate this threat, including
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. These
efforts have not been underway for a
sufficient period to reduce the threat
from contamination, so we retained a
listing priority number of 8 for this
species, reflecting imminent threats of a
moderate magnitude.
Interrupted rocksnail (Leptoxis
foremani (= downei)—The following
summary is based on information
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contained in our files. No new
information was provided in the
petition received on May 11, 2004.
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 to 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. We believe water
quality was the cause of this 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 (ADCNR) released about 3000
juvenile interrupted rocksnails from the
TNARI colony into the Coosa River
above Wetumpka, Elmore County,
Alabama. In 2004 and 2005
approximately 1200 and 3000 juvenile
snails, respectively, from the TNARI
culture were released at the lower Coosa
River site by ADCNR. A small number
of the 2003 hatchery-cultured
interrupted rocksnails were observed in
the vicinity of the release site in 2005.
The magnitude of threat is high for this
species since it is only known from one
naturally occurring site. Despite the
ongoing conservation efforts, threats
remain imminent, as water quality
degradation of the stream is currently
occurring and evident, in that the
natural population has undergone a
precipitous decline. Thus, we assigned
a listing priority of 2 to the interrupted
rocksnail.
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. The
sisi snail is a ground-dwelling species in
the Potaridae family and is endemic to
American Samoa. The species is now
known from a single population on the
island of Tutuila, American Samoa.
This species is currently threatened
by habitat loss and modification and by
predation from nonnative predatory
snails. The decline of the sisi in
American Samoa have resulted, in part,
from loss of habitat to forestry and
agriculture and loss of forest structure to
hurricanes and alien weeds that
establish after these storms. All live sisi
snails have been found in the leaf litter
beneath remaining intact forest canopy.
No snails were found in areas bordering
agricultural plots or in forest areas that
were severely damaged by three
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hurricanes (1987, 1990, and 1991).
Under natural historic conditions, loss
of forest canopy to storms did not pose
a great threat to the long-term survival
of these snails; enough intact forest with
healthy populations of snails would
support dispersal back into newly
regrown canopy forest. However, the
presence of alien weeds such as mile-aminute vine (Mikania micrantha) and
weedy tree species such as Funtumia
elastica may reduce the likelihood that
native forest will re-establish in areas
damaged by the hurricanes. This loss of
habitat to storms is greatly exacerbated
by an expanding agriculture.
Agricultural plots have spread from low
elevation up to middle and some high
elevations on all the islands, greatly
reducing the forest area and thus
reducing the resilience of native forests
and its populations of native snails.
These reductions also increase the
likelihood that future storms will lead to
the extinction of populations or species
that rely on the remaining canopy forest.
In an effort to eradicate the giant African
snail, Euglandia rosea and another alien
predatory snail, Gonaxis kibweziensis,
were introduced in 1980 and 1977,
respectively. Euglandia rosea have
spread throughout the main island of
Tutuila and by 1984 was considered to
be well-established on Tutuila. Gonaxis
kibweziensis is also present on Tutuila
though it seems to be in decline.
Numerous studies show that E. rosea
feeds on endemic island snails
including the sisi, and is a major agent
in their declines and extirpations. At
present, the major threat to long-term
survival of the native snail fauna in
American Samoa is predation by
nonnative predatory snails. There are no
conservation efforts being implemented
to alleviate these threats and all these
threats are ongoing and are therefore
imminent. Since the threats occur
throughout the entire range of the
species, they are of a high magnitude.
Therefore we assigned this species an
LPN of 2.
Diamond Y Spring snail
(Pseudotryonia adamantina) and
Gonzales springsnail (Tryonia
circumstriata)—The following summary
is based on information from our files.
No new information was provided in
the petition received on May 11, 2004.
Diamond Y Spring snail and Gonzales
springsnail are small aquatic snails
endemic to Diamond Y Spring in Pecos
County, Texas. The spring 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
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pumping of groundwater. Additional
threats include water contamination
from accidental releases of petroleum
products, as their habitat is in an active
oil and gas field. Also, a nonnative
aquatic snail (Melanoides sp.) was
recently introduced into the native
snails’ habitat and may compete with
endemic snails for space and resources.
The magnitude of threats is high
because limited distribution of these
narrow endemics makes any impact
from increasing threats (e.g., loss of
springflow, contaminants, nonnative
species) likely to result in the extinction
of the species. These species occur in
one location in an arid region currently
plagued by drought and ongoing aquifer
withdrawals, making the eventual loss
of spring flow an imminent threat of
total habitat loss. Thus, we maintain the
listing priority number of 2 for both
species.
Fragile tree snail (Samoana fragilis)—
The following summary is based on
information contained in our files. No
new information was provided in the
petition received on May 11, 2004. A
tree-dwelling species, the fragile tree
snail is a member of the Partulidae
family of snails and is endemic to the
islands of Guam and Rota (Mariana
Islands). Requiring cool and shaded
native forest habitat, the species is now
known only from a single population on
Rota. This species is currently
threatened by habitat loss and
modification and by predation from
nonnative predatory snails. On Rota,
large numbers of pigs, goats and deer,
along with extensive logging, further
contribute to the expansion of savanna
grasslands and directly alter the
understory plant community and overall
forest microclimate. Savanna grassland
habitat is unsuitable for tree snails.
Predation by the alien rosy carnivore
snail (Euglandina rosea) is a serious
threat to the survival of the fragile tree
snail. Field observations have
established that the rosy carnivore snail
will readily feed on native Pacific island
tree snails, including the Partulidae,
such as those of the Mariana Islands.
The rosy carnivore snail has caused the
extirpation of many populations and
species of native snails throughout the
Pacific islands. All of the threats occur
rangewide and no efforts to control or
eradicate the nonnative predatory snail
species or to reduce habitat loss are
being undertaken. The magnitude of
threats is high because limited
distribution of this narrow endemic
makes any impact from increasing
threats (e.g., nonnative species) likely to
result in the extinction of the species.
The threats are also ongoing and thus
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are imminent. Therefore, we assigned
this species a listing priority number of
2.
Guam tree snail (Partula radiolata)—
The following summary is based on
information contained in our files. No
new information was provided in the
petition received on May 11, 2004. A
tree-dwelling species, the Guam tree
snail is a member of the Partulidae
family of snails and is endemic to the
island of Guam. Requiring cool and
shaded native forest habitat, the species
is now known from only 11 populations
on Guam. This species is currently
threatened by habitat loss and
modification and by predation from
nonnative predatory snails. On Guam,
open agricultural fields and other areas
prone to erosion were seeded with
tangantangan (Leucaena leucocephala)
by the U.S. Military. Tangantangan
grows as a single species stand with no
substantial understory. The
microclimatic condition is dry, with
little accumulation of leaf litter humus
and is particularly unsuitable as Guam
tree snail habitat. In addition, native
forest cannot reestablish and grow
where this alien weed has become
established. Large numbers of pigs,
goats, and deer, along with extensive
logging, further contribute to the
expansion of savanna grasslands and
directly alter the understory plant
community and overall forest
microclimate. Savanna grassland habitat
is unsuitable for tree snails. Predation
by the alien rosy carnivore snail
(Euglandina rosea) is a serious threat to
the survival of the Guam tree snail.
Field observations have established that
the rosy carnivore snail will readily feed
on native Pacific island tree snails,
including the Partulidae, such as those
of the Mariana Islands. The rosy
carnivore snail has caused the
extirpation of many populations and
species of native snails throughout the
Pacific islands. All of the threats occur
range wide and no efforts to control or
eradicate the nonnative predatory snail
species or to reduce habitat loss are
being undertaken. The magnitude of
threats is high because limited
distribution of this narrow endemic
makes any impact from increasing
threats (e.g., nonnative species) likely to
result in the extinction of the species.
The threats are also ongoing and thus
are imminent. Therefore, we assigned
this species a listing priority number of
2.
Humped tree snail (Partula gibba)—
The following summary is based on
information contained in our files. No
new information was provided in the
petition received on May 11, 2004. A
tree-dwelling species, the humped tree
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snail is a member of the Partulidae
family of snails, and was originally
known from the island of Guam and the
Commonwealth of the Northern Mariana
Islands (islands of Rota, 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 widely
distributed tree snail endemic in the
Mariana Islands, remaining population
sizes are often small.
This species is currently threatened
by habitat loss and modification and by
predation from nonnative predatorial
snails. In recent times, remaining
populations of the snail have been
threatened by ongoing development. For
example, a road was cut within the
coastal area containing the remaining
three Guam populations of the snail,
and it is believed that the decline in
these populations may be due to the
indirect effects of this road. Throughout
the Mariana Islands, feral ungulates
(pigs (Sus scrofa), Philippine deer
(Cervus mariannus), cattle (Bos taurus),
water buffalo (Bubalus bubalis), and
goats (Capra hircus)) have caused severe
damage to native forest vegetation by
browsing directly on plants, causing
erosion, and retarding forest growth and
regeneration. This in turn reduces the
quantity and quality of forested habitat
for the humped tree snail. Currently,
populations of feral ungulates are found
on the islands of Guam (deer, pigs, and
water buffalo), Rota (deer and cattle),
Aguiguan (goats), Tinian (cattle), Saipan
(deer, pigs, and cattle), Anatahan (pigs
and goats), Alamagan (goats, pigs, and
cattle), and Pagan (cattle, goats, and
pigs). Goats were eradicated from
Sarigan in 1998 and the humped tree
snail has increased in abundance on
that island, likely in response to the
removal of all the goats. However, the
population of humped tree snails on
Anatahan is likely extirpated due to the
massive volcanic explosions of the
island beginning in 2003 and still
continuing, and the resulting loss of up
to 95 percent of the vegetation on the
island. Predation by the alien rosy
carnivore snail (Euglandina rosea) is
also a serious threat to the survival of
the Humped tree snail. Field
observations have established that the
rosy carnivore snail will readily feed on
native Pacific island tree snails,
including the Partulidae such as those
of the Mariana Islands. The rosy
carnivore snail has caused the
extirpation of many populations and
species of native snails throughout the
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Pacific islands. All of the threats occur
range-wide and no efforts to control or
eradicate the nonnative predatory snail
species or to reduce habitat loss are
being undertaken. The magnitude of
threats is high because limited
distribution of this species makes any
impact from increasing threats (e.g.,
nonnative species) likely to result in the
extinction of the species. The threats are
also ongoing and thus are imminent.
Therefore, we assigned this species a
listing priority number of 2.
Lanai tree snail (Partulina
semicarinata)—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,
P. semicarinata is a member of the
Achatinellidae family of snails.
Endemic to the island of Lanai, the
species is currently known from 3
populations totaling 29 individuals.
This species is highly threatened
throughout its limited range by habitat
loss and modification and by predation
from rats. No efforts are being
undertaken to remove rats in areas that
P. semicarinata occur. The threat from
this predator is expected to continue or
increase unless the rats are actively
controlled or eradicated. Habitat loss
also continues due to the trampling and
browsing of native vegetation required
by P. semicarinata by nonnative
ungulates. Although the snails are in an
area to be fenced, until the fence is
constructed and the ungulates have
been removed, the habitat will continue
to be degraded. The small number of
individuals and the small number of
populations make this species very
susceptible to the negative effects of
stochastic events such as hurricanes and
storms. There is a population in
captivity that is protected from the
effects of unexpected droughts, though
the effects of severe storms may still
affect this population as evidenced by
the loss of snails when a severe flood
interrupted the power supply to the
University and temperatures increased
within the environmental chambers
containing the snails. In addition, these
snails are likely subjected to the same
concerns of reproductive vigor and loss
of genetic variability. The magnitude of
threats is high because limited
distribution of this narrow endemic
makes any impact from increasing
threats (e.g., nonnative species) likely to
result in the extinction of the species.
The threats are also ongoing and thus
are imminent. Therefore, we assigned
this species a listing priority number of
2.
Lanai tree snail (Partulina
variabilis)—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. A tree-dwelling species, P.
variabilis is a member of the
Achatinellidae family of snails.
Endemic to the island of Lanai, the
species is currently known from 12
populations totaling 90 individuals.
This species is highly threatened
throughout its limited range by habitat
loss and modification and by predation
from rats. No efforts are being
undertaken to remove rats in areas that
P. variabilis occur. The threat from this
predator is expected to continue or
increase unless the rats are actively
controlled or eradicated. Habitat loss
also continues due to the trampling and
browsing of native vegetation required
by P. variabilis by nonnative ungulates.
Although the snails are in an area to be
fenced, until the fence is constructed
and the ungulates have been removed,
the habitat will continue to be degraded.
The small number of individuals and
the small number of populations make
this species very susceptible to the
negative effects of stochastic events
such as hurricanes and storms. There is
a population in captivity that is
protected from the effects of unexpected
droughts, though the effects of severe
storms may still affect this population as
evidenced by the loss of snails when a
severe flood interrupted the power
supply to the University and
temperatures increased within the
environmental chambers containing the
snails. In addition, these snails are
likely subjected to the same concerns of
reproductive vigor and loss of genetic
variability as the wild population. The
magnitude of threats is high because
limited distribution of this narrow
endemic makes any impact from
increasing threats (e.g., nonnative
species) likely to result in the extinction
of the species. The threats are also
ongoing and thus are imminent.
Therefore, we assigned this species a
listing priority number of 2.
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 is a member of the
Partulidae family of snails and is known
from one population on the island of
Aguiguan. This species is currently
threatened by habitat loss and
modification and by predation from
nonnative predatorial snails. In the
1930s, the island of Aguiguan was
mostly cleared of native forest to
support sugar cane and pineapple
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production. The abandoned fields and
airstrip are now overgrown with alien
weeds. The remaining native forest
understory has greatly suffered from
large and uncontrolled populations of
alien goats and the invasion of weeds.
Goats (Capra hircus) have caused severe
damage to native forest vegetation by
browsing directly on plants, causing
erosion, and retarding forest growth and
regeneration. This in turn reduces the
quantity and quality of forested habitat
for Langford’s tree snail. Predation by
the alien rosy carnivore snail
(Euglandina rosea) is also a serious
threat to the survival of Langford’s tree
snail. Field observations have
established that the rosy carnivore snail
will readily feed on native Pacific island
tree snails, including the Partulidae
such as those of the Mariana Islands.
The rosy carnivore snail has caused the
extirpation of many populations and
species of native snails throughout the
Pacific islands. All of the threats occur
rangewide and no efforts to control or
eradicate the nonnative predatory snail
species or to reduce habitat loss are
being undertaken. The magnitude of
threats is high because limited
distribution of this narrow endemic
makes any impact from increasing
threats (e.g., nonnative species) likely to
result in the extinction of the species.
The threats are also ongoing and thus
are imminent. Therefore, we assigned
this species a listing priority number of
2.
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. Phantom Cave snail and
Phantom springsnail are small aquatic
snails that occur in three spring
outflows in the Toyah Basin in Reeves
and Jeff Davis Counties, Texas. The
primary threat to both species is the loss
of surface flows due to declining
groundwater levels from drought and
pumping for agricultural production.
Although much of the land immediately
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 their habitat has
declined due to a reduction in spring
flows, possibly as a result of private
groundwater pumping in areas beyond
that controlled by these landowners. As
an example, Phantom Lake Spring, one
of the sites of occurrence, has already
ceased flowing and aquatic habitat is
supported only by a pumping system.
The magnitude of the threats is high
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because spring flow loss would result in
complete habitat destruction and
permanent elimination of all
populations of the species. The
immediacy of the threats is imminent,
as evidenced by the drastic decline in
spring flow at Phantom Lake Spring that
is happening now and will likely
extirpate this population in the near
future. Declining spring flows in San
Solomon Spring are also becoming
evident and will affect that spring site
as well within the foreseeable future.
Thus, we maintained the listing priority
number of 2 for both 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 is a member of the Partulidae
family of snails 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 predatory
snails. All live Tutuila tree snails were
found on understory vegetation beneath
remaining intact forest canopy. No
snails were found in areas bordering
agricultural plots or in forest areas that
were severely damaged by three
hurricanes (1987, 1990, and 1991).
Under natural historical conditions, loss
of forest canopy to storms did not pose
a great threat to the long-term survival
of these snails; enough intact forest with
healthy populations of snails would
support dispersal back into newly
regrown canopy forest. However, the
presence of alien weeds such as mile-aminute vine (Mikania micrantha) and
weedy tree species such as Funtumia
elastica, may reduce the likelihood that
native forest will re-establish in areas
damaged by the hurricanes. This loss of
habitat to storms is greatly exacerbated
by an expanding agricultural footprint.
Agricultural plots have spread from low
elevation up to middle and some high
elevations on all the islands, greatly
reducing the forest area and thus
reducing the resilience of native forests
and its populations of native snails.
These reductions also increase the
likelihood that future storms will lead to
the extinction of populations or species
that rely on the remaining canopy forest.
In an effort to eradicate the giant African
snail, Euglandina rosea and another
alien predatory snail, Gonaxis
kibweziensis, were introduced in 1980
and 1977, respectively. Euglandia rosea
have spread throughout the main island
of Tutuila and by 1984, was considered
to be well established on Tutuila.
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Gonaxis kibweziensis is also present on
Tutuila though it seems to be in decline.
Numerous studies show that E. rosea
feeds on endemic island snails,
including the Tutuila tree snail, and is
a major agent in their declines and
extirpations. At present, the major threat
to the long-term survival of the native
snail fauna in American Samoa is
predation by nonnative predatory snails.
There are currently no conservation
efforts being implemented to alleviate
the threats to this species. The
magnitude of threats is high because
limited distribution of this narrow
endemic makes any impact from
increasing threats (e.g., nonnative
species) likely to result in the extinction
of the species. The threats are also
ongoing and thus are imminent.
Therefore, we assigned this species a
listing priority number of 2.
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 the threats are ongoing (e.g.,
grazing of cattle, water withdrawal, and
fire). Therefore, due to the continuing
high magnitude and imminence of
threats to this species, we retained a
listing priority number of 2 for this
species.
Elongate mud meadows springsnail
(Pyrgulopsis notidicola)—The following
summary is based on information
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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 affect 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
retained 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
(i.e., 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 long-term
survival of the Gila springsnail at risk.
Natural events such as drought, forest
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
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activities and fire retardant chemicals
have potentially deleterious effects on
this species. Because several of the
springs occur on U.S. 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 affect
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 affected aquatic life
in streams. If the drought continues or
worsens, the imminence of threats from
decreased discharge or fire will
increase. Based on these nonimminent
threats that are currently of a low
magnitude, we retained a listing priority
number of 11 for this species.
Gonzales springsnail (Tryonia
circumstriata)—See paragraph above
under Diamond Y Spring snail
(Pseudotryonia adamantina).
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 this
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
nonimminent threats of a high
magnitude, we retained 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
populations associated with a series of
spring-brook systems along the Gila
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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 (i.e., 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. 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 can 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 affect
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 affected aquatic life in streams.
If the drought continues or worsens, the
imminence of threats from decreased
discharge and fire will increase. Based
on these nonimminent threats of a low
magnitude, we retained 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
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 Arizona Game
and Fish Department and Service
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biologists no longer entails snail
removal, which appears to have had a
temporary positive impact on
population numbers. The threat of
groundwater withdrawal is not
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.
However, the magnitude of threats is
high because limited distribution of this
narrow endemic makes any impact from
the threat (e.g., groundwater
withdrawal) likely to result in the
extinction of the species. Therefore, we
retained 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 U.S.
Fish and Wildlife Service and U.S.
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 the long-term, the
threats are ongoing and therefore,
imminent. The magnitude of threats is
high because limited distribution of this
narrow endemic makes any impact from
the threats likely to result in the
extinction of the species. Therefore, we
retained a listing priority number of 2
for the Three Forks springsnail.
Newcomb’s tree snail (Newcombia
cumingi)—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,
Newcomb’s tree snail is a member of the
snail family, Achatinellidae. The
species is endemic to the island of
Maui, where it is currently known from
a single remaining population. The
greatest threats to the Newcomb’s tree
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snail are the loss of the only known
remaining population due to stochastic
events and predation from rats and
Euglandina rosea. There are no efforts
being made to reduce the threat from the
carnivorous snail and only minimal rat
control in the area occupied by this
snail. Our attempts to raise this species
in a captive propagation facility have
been unsuccessful. We have assigned a
listing priority number of 2 for this
species because threats are occurring in
the only known remaining population
making it of high magnitude and
because the threats are ongoing which
make them imminent.
Insects
Warm Springs Zaitzevian riffle beetle
(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 riffle
beetle is an aquatic flightless beetle
endemic to a single warm spring in
southwestern Montana whose surface
area is approximately 35 square meters.
Because of its naturally limited range,
this riffle beetle is at risk of randomly
occurring natural- and human-caused
events. The warm spring is under the
jurisdiction of the Service, which built
a structure that provides a considerable
level of physical protection for the
warm spring. Because of the physical
and jurisdictional protection, we
determined that the magnitude of
threats is low and the threats are
nonimminent. Based on this, we
assigned this species a listing priority
number of 11.
Wekiu bug (Nysius wekiuicola)—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.
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 that feeds
upon two host plants, Procris
pedunculata and Elatostema calcareum.
Endemic to the islands of Guam and
Saipan, the species is now known from
ten populations on Guam. This species
is currently threatened by alien
predation and parasitism and impacts to
its host plants by browsing ungulates.
The Mariana eight spot butterfly has
extremely high mortality of eggs and
larvae due to predation by alien ants
and wasps. Nonnative deer degrade the
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habitat by browsing, trampling, and
uprooting the butterfly’s host plants.
The threats of habitat loss by nonnative
deer, and parasitism and predation by
nonnative insects occur range-wide. The
magnitude of threats is high because
limited distribution of this narrow
endemic makes any impact from these
threats likely to result in the extinction
of the species. Direct threats to the
Mariana eight spot butterfly from alien
predators and parasites and indirect
threats from impacts to its host plants
by browsing ungulates are all imminent
because they have been occurring for
many years and are ongoing. Therefore,
we assigned 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
from and endemic to the islands of
Guam and Rota, the species is now
known only from one population on
Rota. This species is currently
threatened by alien predation and
parasitism and impacts to its host plants
by browsing ungulates. The Mariana
wandering butterfly has extremely high
mortality of eggs and larvae due to
predation by alien ants and wasps.
Nonnative deer degrade the habitat by
browsing, trampling, and uprooting the
butterfly’s host plants. The threats of
habitat loss by nonnative deer, and
parasitism and predation by nonnative
insects occur range-wide. The
magnitude of threats is high because
limited distribution of this narrow
endemic makes any impact from these
threats likely to result in the extinction
of the species. Direct threats to the
Mariana wandering butterfly from alien
predators and parasites and indirect
threats from impacts to its host plants
by browsing ungulates are all imminent
because they have been occurring for
many years and are ongoing. Therefore,
we assigned a listing priority number of
2 for this species.
Miami blue butterfly (Cyclargus
thomasi bethunebakeri)—The following
summary is based on information
contained in our files and in the petition
received on June 15, 2000. The Miami
blue appears to be endemic to south
Florida. Historically, it occurred
throughout the Florida Keys, north to
Hillsborough and Volusia Counties.
None were documented between 1996
and 1999. In 1999, an extant population
was discovered at Bahia Honda State
Park on Bahia Honda Key. It is now
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restricted to that park, other than several
larvae that were documented on West
Summerland Key, on unprotected land
approximately 2.2 miles west of the
Bahia Honda site, in November 2003.
This butterfly occupies about 1.28 acres
on Bahia Honda. The Miami blue is
predominantly a coastal species,
occurring in disturbed and early
successional habitats such as the edges
of tropical hardwood hammock, coastal
berm forest, and along trails and other
open sunny areas, and historically in
pine rocklands. These habitats provide
larval host plants and adult nectar
sources that are required to occur in
close juxtaposition, due to the very
restricted range of movement exhibited
by the butterfly. The magnitude of threat
is high for this species, due to threats
associated with limited population size
and range, mosquito control activities,
and hurricanes. The threats are
nonimminent since the current range is
within a state park wherein threats from
mosquito control actions are
substantially controlled, and because
threats associated with small population
size and stochastic events (like
hurricanes) are long-term, not
immediate threats. Therefore, the Miami
blue is assigned a listing priority
number of 6.
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 retained a
listing priority number of 5 for this
species.
Beaver Cave beetle
(Pseudanophthalmus major)—The
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following summary is based upon
information in our files. No new
information was provided in the
petition received on May 11, 2004.
Beaver Cave beetle is a small, eyeless,
reddish-brown predatory insect that
feeds upon small cave invertebrates. It
is cave dependent and is not found
outside the cave environment. The
Beaver Cave beetle is only known from
one privately owned Kentucky cave.
The limestone cave in which this
species is found provide a unique and
fragile environment that supports a
variety of species that have evolved to
survive and reproduce under the
demanding conditions found in cave
ecosystems. The species was observed
in 2005 during a survey of the cave. The
limited distribution of the species
makes it vulnerable to isolated events
that would only have a minimal effect
on more wide-ranging insects. Events
such as toxic chemical spills, discharges
of large amounts of polluted water or
indirect impacts from off-site
construction activities, closure of
entrances, alteration of entrances, or the
creation of new entrances could have
serious adverse impacts on this species.
The likelihood of one of the events
eventually occurring combined with the
narrow range of the species makes the
magnitude of threats high. The
immediacy of threat is nonimminent
because there are no known projects
planned that would affect the species in
the next 1 to 2 years; we therefore have
assigned a listing priority number of 5
to this species.
Clifton cave beetle
(Pseudanophthalmus caecus)—The
following summary is based upon
information in our files. No new
information was provided in the
petition received on May 11, 2004.
Clifton cave beetle is a small, eyeless,
reddish-brown predatory insect that
feeds upon small cave invertebrates. It
is cave dependent and is not found
outside the cave environment. Clifton
cave beetle is only known from two
privately owned Kentucky caves. Soon
after the species was first collected in
1963 the entrance to the cave was sealed
due to road construction. Other caves in
the vicinity of this cave were surveyed
for the species during a 1995 to 1996.
Only one additional site was found to
support the Clifton Cave beetle. It can
not be determined at this time if the
species still occurs at the original
location or if the species has been
extirpated from the site by the closure
of the cave entrance. The limestone
caves in which this species are found
provide a unique and fragile
environment that supports a variety of
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species that have evolved to survive and
reproduce under the demanding
conditions found in cave ecosystems.
The limited distribution of the species
makes it vulnerable to isolated events
that would only have a minimal effect
on the more wide-ranging insects.
Events such as toxic chemical spills,
discharges of large amounts of polluted
water or indirect impacts from off-site
construction activities, closure of
entrances, alteration of entrances, or the
creation of new entrances could have
serious adverse impacts on this species.
The likelihood of one of the events
eventually occurring combined with the
narrow range of the species makes the
magnitude of threats high. The
immediacy of threat is nonimminent
because there are no known projects
planned that would affect the species in
the next 1 to 2 years; we therefore
assigned a listing priority number of 5
to this species.
Icebox cave beetle
(Pseudanophthalmus frigidus)—The
following summary is based upon
information in our files. No new
information was provided in the
petition received on May 11, 2004.
Icebox cave beetle is a small, eyeless,
reddish-brown predatory insect that
feeds upon small cave invertebrates. It
is cave dependent and is not found
outside the cave environment. Icebox
cave beetle is only known from one
privately owned Kentucky cave. The
limestone cave in which this species is
found provides a unique and fragile
environment that supports a variety of
species that have evolved to survive and
reproduce under the demanding
conditions found in cave ecosystems.
The species has not been observed since
it was originally collected from the only
site known to support the species, but
species experts believe that it may still
exist there in low numbers. The limited
distribution of the species makes it
vulnerable to isolated events that would
only have a minimal effect on the more
wide-ranging insects. Events such as
toxic chemical spills, discharges of large
amounts of polluted water or indirect
impacts from off-site construction
activities, closure of entrances,
alteration of entrances, or the creation of
new entrances could have serious
adverse impacts on this species. The
likelihood of one of the events
eventually occurring combined with the
narrow range of the species makes the
magnitude of threats high. The
immediacy of threat is nonimminent
because there are no known projects
planned that would affect the species in
the next 1 to 2 years; we therefore have
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assigned a listing priority number of 5
to this species.
Inquirer cave beetle
(Pseudanophthalmus inquisitor)—The
following summary is based upon
information in our files. No new
information was provided in the
petition received on May 11, 2004. The
inquirer cave beetle is a fairly small,
eyeless, reddish-brown predatory insect
that feeds upon small cave
invertebrates. It is cave dependent and
is not found outside the cave
environment. The inquirer cave beetle is
only known from one privately owned
Tennessee cave. The limestone cave in
which this species is found provides a
unique and fragile environment that
supports a variety of species that have
evolved to survive and reproduce under
the demanding conditions found in cave
ecosystems. The species was last
observed in 1997. The limited
distribution of the species makes it
vulnerable to isolated events that would
only have a minimal effect on the more
wide-ranging insects. The area around
the only know site for the species is in
a rapidly expanding urban area and
indirect impacts, such as chemical or
other pollution, could significantly
affect both the cave and the species the
cave supports. The entrance to the cave
is protected by the landowner through
a cooperative management agreement
with the Service, The Nature
Conservancy, and Tennessee Wildlife
Resources Agency; however, a sinkhole
that drains into the cave system is
located away from the protected
entrance and is near a highway. Events
such as toxic chemical spills, discharges
of large amounts of polluted water or
indirect impacts from off-site
construction activities could adversely
affect the species. The likelihood of one
of the events eventually occurring
combined with the narrow range of the
species makes the magnitude of threats
high. The immediacy of threat is
nonimminent because there are no
known projects planned that would
affect the species in the next 1 to 2 years
and it receives some protection under a
cooperative management agreement; we
therefore have assigned a listing priority
number of 5 to this species.
Louisville cave beetle
(Pseudanophthalmus troglodytes)—The
following summary is based upon
information in our files. No new
information was provided in the
petition received on May 11, 2004. The
Louisville cave beetle is a small, eyeless,
reddish-brown predatory insect that
feeds upon cave invertebrates. It is cave
dependent and is not found outside the
cave environment. Louisville cave
beetle is only known from two privately
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owned Kentucky caves. The limestone
caves in which this species 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 limited distribution of the species
makes it vulnerable to isolated events
that would only have a minimal effect
on the more wide-ranging insects.
Events such as toxic chemical spills,
discharges of large amounts of polluted
water or indirect impacts from off-site
construction activities, closure of
entrances, alteration of entrances, or the
creation of new entrances could have
serious adverse impacts on this species.
The likelihood of one of the events
eventually occurring combined with the
narrow range of the species makes the
magnitude of threats high. The
immediacy of threat is nonimminent
because there are no known projects
planned that would affect the species in
the next 1 to 2 years; we therefore have
assigned a listing priority number of 5
to this 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 was
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 and
imminence of the threat to the
surprising cave beetle is reduced
because of its location on Federal land
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and the implementation of a Candidate
Conservation Agreement between
MCNP and the Service to protect the
species. Therefore we have assigned a
listing priority of 11 to this species.
Tatum Cave beetle
(Pseudanophthalmus parvus)—The
following summary is based upon
information in our files. No new
information was provided in the
petition received on May 11, 2004.
Tatum Cave beetle is a small, eyeless,
reddish-brown predatory insect that
feeds upon cave invertebrates. It is cave
dependent and is not found outside the
cave environment. Tatum Cave beetle is
only known from one privately owned
Kentucky cave. The limestone cave in
which this species is found provides a
unique and fragile environment that
supports a variety of species that have
evolved to survive and reproduce under
the demanding conditions found in cave
ecosystems. The species has not been
observed since 1965 but species experts
believe that it still exists in low
numbers. The limited distribution of the
species makes it vulnerable to isolated
events that would only have a minimal
effect on the more wide-ranging insects.
Events such as toxic chemical spills,
discharges of large amounts of polluted
water or indirect impacts from off-site
construction activities, closure of
entrances, alteration of entrances, or the
creation of new entrances could have
serious adverse impacts on this species.
The likelihood of one of the events
eventually occurring combined with the
narrow range of the species makes the
magnitude of threats high. The
immediacy of threat is nonimminent
because there are no known projects
planned that would affect the species in
the next 1 to 2 years; we therefore have
assigned a listing priority number of 5
to 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, the
Taylor’s checkerspot butterfly was
known from 70 locations: 23 in British
Columbia, 34 in Washington, and 13 in
Oregon. Following surveys during the
2005 flight period, only 15 populations
were confirmed, with a total of about
2,500 to 3,000 individuals observed.
Twelve populations are known from
Washington, two in the Willamette
Valley of Oregon and the new location
found in British Columbia, Canada. The
species was thought to have been
extirpated in Canada until this new
population was discovered at a new
location on Denman Island, British
Columbia.
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Threats include degradation and
destruction of native grasslands by
conversion to agriculture, residential
development, commercial purposes,
encroachment by nonnative plants, and
natural 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. Magnitude of
threats is high because of the extremely
small size of remaining populations and
reduction in distribution from the
historical range and because the threats
may occur at all or a major portion of
the known butterfly locations. The size
and location of the populations shift
from year to year. Threats are imminent
because they are currently occurring.
The ecosystem on which this subspecies
depends requires annual management to
maintain its grassland habitat. We
assigned the Taylor’s checkerspot
butterfly a listing priority number of 3.
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. The
blackline Hawaiian damselfly 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 alien
aquatic species such as fish and
predacious insects and habitat loss
through dewatering of streams and
invasive nonnative plants. Nonnative
fish and insects prey on the naiads of
the damselfly and loss of water reduces
the amount of suitable naiad habitat
available. Invasive plants also
contribute to loss of habitat by either
over shading streams or by forming
dense, monotypic stands that
completely eliminate any open water
(e.g. California grass (Brachiaria
mutica)). These threats are occurring in
varying degrees range-wide for the
blackline Hawaiian damselfly. Although
there are no efforts being done to control
or eradicate nonnative fish or insects or
to stop the loss of habitat, the 11 streams
are widely dispersed on both sides of
the mountain range and are highly
unlikely to experience complete loss of
populations at the same time. Therefore
the magnitude of the threats is
moderate. Threats to the blackline
Hawaiian damselfly from loss of habitat
and introduced nonnative fish and
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insects are ongoing and therefore are
imminent. Therefore, we assigned this
subspecies a listing priority number of
9.
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 alien aquatic species
such as fish and predacious insects and
habitat loss through dewatering of
streams and invasive plant species.
Nonnative fish and insects prey on the
naiads of the damselfly and loss of
water reduces the amount of suitable
naiad habitat available. Invasive plants
also contribute to loss of habitat by
either over shading streams or by
forming dense, monotypic stands that
completely eliminate any open water
(e.g. California grass (Brachiaria
mutica)). There are no conservation
measures being taken to alleviate these
threats for this species. Nonnative fish
and plants are found in all the streams
the crimson Hawaiian damselfly occurs
in making these threats ongoing and
imminent. These threats are of high
magnitude because of their severity and
because they are occurring throughout
its limited range. We have assigned this
species a listing priority number of 2
because the threats are of a high
magnitude and are imminent.
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 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
that likely feed on both naiads and
emerging adults, and habitat loss due to
disturbance by feral ungulates. While
foraging, pigs root and trample the forest
floor, encouraging the establishment of
nonnative plants in the newly disturbed
soil. In moist depressions, pigs
completely remove all vegetation by
wallowing, leaving nothing but mud
and water. The complete removal of
vegetation as well as the establishment
of nonnative plants destroy the leaf
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litter habitat that is likely used by the
Flying earwig Hawaiian damselfly
naiads. These threats are ongoing in the
only known population of this species
and no conservation efforts are being
done to alleviate these serious threats
for this species. We assigned this
species a listing priority number of 2
because the threats are of a high
magnitude and are imminent.
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 alien
aquatic species such as fish and
predacious insects and habitat loss
through dewatering of streams and
invasion by nonnative plants. Nonnative
fish and insects prey on the naiads of
the damselfly and loss of water reduces
the amount of suitable naiad habitat
available. Invasive plants also
contribute to loss of habitat by either
over shading streams or by forming
dense, monotypic stands that
completely eliminate any open water
(e.g. California grass (Brachiaria
mutica)). There are no conservation
measures being taken to alleviate these
threats for this species. Nonnative fish
and plants are found in all the streams
the oceanic Hawaiian damselfly occurs
in making these threats ongoing and
imminent. These threats are of high
magnitude because of their severity and
because they are occurring throughout
its limited range. Therefore, we have
assigned this species a listing priority
number of 2.
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
alien aquatic species such as fish and
predacious insects and habitat loss
through dewatering of streams and
invasion by nonnative plants. Nonnative
fish and insects prey on the naiads of
the damselfly and loss of water reduces
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the amount of suitable naiad habitat
available. Invasive plants also
contribute to loss of habitat by either
overshading streams or by forming
dense, monotypic stands that
completely eliminate any open water
(e.g. California grass (Brachiaria
mutica)). Nonnative fish and plants are
found in all the streams the orangeblack
damselfly occur in, except the Oahu
location, where there are no nonnative
fish, making these threats ongoing and
imminent. Although no conservation
efforts are being implemented for this
species in particular on Molokai, Lanai,
and the island of Hawaii, the Oahu
location is located at Tripler Army
Medical Center. The Army has
consistently considered the damselfly’s
needs in all work done near or in the
stream and maintains a supplemental
water flow into the stream to maintain
habitat after disrupting the original
flow. We assigned this species a listing
priority number of 8 because though the
threats are imminent, they are of
moderate magnitude given the more
widely dispersed population and the
conservation efforts at Tripler.
Pacific Hawaiian damselfly
(Megalagrion pacificum)—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 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 alien aquatic species,
such as fish and predacious insects, and
habitat loss through dewatering of
streams and invasion by nonnative
plants. Nonnative fish and insects prey
on the naiads of the damselfly and loss
of water reduces the amount of suitable
naiad habitat available. Invasive plants
also contribute to loss of habitat by
either overshading streams or by
forming dense, monotypic stands that
completely eliminate any open water
(e.g. California grass (Brachiaria
mutica)). There are no conservation
measures being taken to alleviate these
threats for this species. Nonnative fish
and plants are found in all the streams
the Pacific Hawaiian damselfly occurs
in making these threats ongoing and
imminent. These threats are of high
magnitude because of their severity and
because they are occurring throughout
its limited range. Therefore, we have
assigned this species a listing priority
number of 2.
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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, a member
of the fly family Drosophilidae, 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. While
foraging, pigs root and trample the forest
floor, encouraging the establishment of
nonnative plants in the newly disturbed
soil. Pigs also disseminate nonnative
plant seeds through their feces and on
their bodies, accelerating the spread of
nonnative plants through native forest.
These nonnative plants often displace
native plants including the host plant
this species depends on. Feral goats also
consume native vegetation including
this species’ host plant, trample roots
and seedlings, accelerate erosion, and
promote the invasion of nonnative
plants. Additionally, nonnative insect
species prey on and parasitize both the
larvae and adult phases of the picture
wing fly. All these threats are ongoing
which make them imminent and are
severe throughout the species range
which makes the threats of high
magnitude. Therefore, we assigned this
species a listing priority number of 2.
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, a member
of the fly family Drosophilidae, 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. While
foraging, pigs root and trample the forest
floor, encouraging the establishment of
nonnative plants in the newly disturbed
soil. Pigs also disseminate nonnative
plant seeds through their feces and on
their bodies, accelerating the spread of
nonnative plants through native forest.
These nonnative plants often displace
native plants including the host plant
this species depends on. Feral goats also
consume native vegetation including
this species host plant, trample roots
and seedlings, accelerate erosion, and
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promote the invasion of nonnative
plants. Additionally, nonnative insect
species prey on and parasitize both the
larvae and adult phases of the picture
wing fly. All these threats are ongoing
which make them imminent and are
sever throughout the range of this
species which makes the threats of high
magnitude. Therefore, we assigned this
species a listing priority number of 2.
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 ci,negas.
Threats are largely from habitat
modification; we consider them to be of
high magnitude due to the limited range
of the species. 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 retained 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 occupied States.
The species is threatened by
conversion of its native prairie habitat
for agricultural purposes, overgrazing,
invasive species, gravel mining,
inbreeding, population isolation, and, in
some cases, prescribed fire. In addition,
prairie succeeds to shrubland or forest
without periodic fire, grazing, or
mowing; thus, the species is also
threatened at sites where such
disturbances are not applied. 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 Service,
other agencies, and private
organizations (e.g., The Nature
Conservancy) protect and manage some
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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 Dakota skipper. The
threats are such that the species
warrants listing; the threats are
moderate in magnitude and, although
some sites are imminently threatened,
overall the threats are nonimminent.
Therefore, we assigned a listing priority
number of 11 to the 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 rare
northwestern butterfly with a
remarkably 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, and fire suppression; and direct
loss of individuals due to fire,
recreational activities, insect collecting,
and random, naturally occurring events.
Limited dispersal ability restricts the
likelihood of recolonization once a
population is lost. The magnitude of
threats is high because of the small
population sizes and disjunct
distribution of the species that limits its
ability to disperse; just 10 of the known
locations for Mardon Skipper have more
than 50 individuals. Loss of any of the
populations could threaten the
continued existence of the species
within each of its known separate
locales. However, the number of
documented locations for the species
has increased from less than 10 in 1998
to as many as 65 rangewide in 2005 and
it would be unlikely to have threats that
would affect all known locales
simultaneously. Overall, we consider
the threats to be nonimminent because
the threats are not currently occurring at
all known population sites. We have
assigned a listing priority number of 5
to 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 occurs
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only at the Coral Pink Sand Dunes,
approximately seven miles west of
Kanab, Kane County, in south-central
Utah. It is restricted to a small part of
the 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
use that is destroying and degrading the
beetle’s habitat, especially the
interdunal swales used by the larvae.
The continued survival of the beetle
depends on the preservation of its
habitat. The two agencies that manage
the dunes field, the Utah Department of
Parks and Recreation and the Bureau of
Land Management, have restricted
recreational off-road vehicle use in some
areas, which reduces impacts. The
beetle’s population is also vulnerable to
over collecting by professional and
hobby tiger-beetle collectors.
Quantification of this threat is difficult
without continuous population
monitoring. Climatic factors, most
recently drought conditions, have
reduced the population, but it has
shown some recent improvement. Based
on imminent threats of a low to
moderate magnitude, we retained a
listing priority of 9.
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. The Highlands tiger beetle is
narrowly distributed and 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. This tiger beetle has
been found at 40 sites from near Haines
City south to Josephine Creek. In the
most recent survey, biologists found a
total of 1,574 adults at 40 sites
compared with 643 adults at 31 sites in
1996, 928 adults at 31 sites in 1995, and
742 adults at 21 sites in 1993. Of the 40
sites in the 2004–2005 surveys with one
or more adults: Three sites were found
to have large populations of over 100
adults [Catfish Creek Preserve (493),
Snell Creek South (193), and Flaming
Arrow Scout Camp (175)]; three sites
had populations of 50–99 adults; eight
sites had 20–49 adults, 13 sites had 10–
19 adults, and 13 sites had < 10 adults.
Results from a limited removal study at
four sites suggest that the actual
population size at the various survey
sites is likely to be as much as two times
as high as indicated by the visual index
counts. Lack of fire to create open sand,
pesticide use, small population sizes at
some sites, and over-collecting pose
serious threats to this species. Because
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this species is narrowly distributed with
specific habitat requirements and small
populations, the magnitude of threats is
high. Although the majority of its
historic range has been lost, degraded,
and fragmented, numerous sites are now
protected, and land managers are
implementing prescribed fire, which
should restore habitat and help reduce
threats. Overall, the threats are
nonimminent. Therefore, the Highlands
tiger beetle is assigned a listing priority
number of 5.
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, or
has been received since the last
Candidate Notice of Review published
on May 11, 2005. Warton’s Cave
meshweaver is an eyeless, cavedwelling, unpigmented, 0.25 inch long
invertebrate known only from female
specimens. This meshweaver is known
to occur in only one cave (Pickle Pit) in
Travis County, Texas. Primary threats to
the species and its habitat are predation
and competition from fire ants and
surface and subsurface effects from
runoff from an adjacent subdivision.
The magnitude of threats is high
because the single location for this
species makes it highly vulnerable to
extinction. The threats are imminent
because fire ants are known to occur in
the vicinity of the cave, and impacts to
the cave from runoff and human
activities are an imminent threat. Thus,
we assign a listing priority number of 2
to this species.
Crustaceans
Anchialine pool shrimp (Metabetaeus
lohena)—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.
Anchialine pool shrimp
(Palaemonella burnsi)—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.
Anchialine pool shrimp (Procaris
hawaiana)—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.
Anchialine pool shrimp (Vetericaris
chaceorum)—See above in ‘‘Summary of
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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. It is classified as a troglobite,
or obligatory cave organism, of which its
most extraordinary feature is the
reduction or loss of vision and
pigmentation. They feed on organic
waste material and debris, such as bat
guano. Little is known concerning the
status of T. monae in either Barbuda or
Dominican Republic. Although in
Puerto Rico this species was previously
found at Mona Island, currently T.
monae is known from only three caves
within the Gurca Commonwealth Forest
in the municipalities of Gurca, Yauco,
and Guayanilla. However, the species
may still be found in the reef deposit
aquifers in Mona Island that have not
yet been surveyed. In 1995, the
population in Puerto Rico was estimated
to be close to 2,000 individuals; over
95% of these were observed in only one
cave. Changes in groundwater quality,
collection of rare animals, predation,
limited distribution of the species,
limited availability of appropriate
habitat (i.e., underground aquifers
within cave formations), potential
reduction of food sources (e.g., mortality
or reduction in bat populations), and
low population numbers, threaten
populations of T. monae. These threats
are not imminent because the known
range of T. monae is within protected
lands and there are no known projects
or management activities planned
within the Gurca Commonwealth Forest
or Mona Island that would result in
mortality of this species. The magnitude
of threat to T. monae is high due to its
restricted distribution, low population
numbers, and aggregation of most
individuals at only one location.
Therefore, we assign a listing priority
number of 5 to this species.
Flowering Plants
Abronia alpina (Ramshaw Meadows
sand-verbena)—See above in ‘‘Summary
of Listing Priority Changes in
Candidates.’’ No new information was
provided in the petition received on
May 11, 2004.
Arabis georgiana (Georgia
rockcress)—See above in ‘‘Summary of
Listing Priority Changes in Candidates.’’
The above summary is based on
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information contained in our files. No
new information was provided in the
petition received on May 11, 2004.
Argythamnia blodgettii (Blodgett’s
silverbush)—The following summary is
based on information in our files. No
new information was provided in the
petition received on May 11, 2004.
Blodgett’s silverbush has been found in
open, sunny areas in pine rockland,
edges of rockland hammock, edges of
coastal berm, and sometimes disturbed
areas at the edges of natural areas.
Plants can be found growing from
crevices on limestone, or on sand. The
pine rockland habitat where it occurs in
Miami-Dade County and the Florida
Keys requires periodic fires to maintain
habitat with a minimum amount of
hardwoods. Approximately 10,000
plants may exist at 18 sites, with most
of the plants on the large pinelands of
Long Pine Key in Everglades National
Park and Big Pine Key (in part on
National Key Deer Refuge), as well as
other smaller pinelands on conservation
lands. If this plant’s distribution were
limited to the mainland, we would
consider the magnitude of threat to be
high due to exotic pest plant problems
in the Miami-Dade urban and
agricultural area, and the likely arrival
of a serious new pest, Old World
climbing fern. Because the Keys are
drier and perhaps less fertile, managing
vegetation is slightly easier. Fire return
intervals are longer and Old World
Climbing fern may prove to be less of a
threat. As a result, we consider the
magnitude of threats to be moderate to
low. We are maintaining the immediacy
of threat as nonimminent to reflect the
intensive management and biological
control efforts already aimed at Old
World climbing fern, as well as the
quality of management on conservation
lands. Thus, we assigned a listing
priority number of 11 to this species.
Artemisia campestris 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 declining; it is
unclear whether the Grant County
population is stable or declining, but it
is vulnerable to environmental
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variability. Surveys of apparently
suitable habitat along the Hanford Reach
have not detected any additional plants.
Threats to northern wormwood
include direct loss of suitable habitat
through regulation of water levels in the
Columbia River and placement of riprap
along the river bank; trampling of plants
as a result of recreational use;
competition with nonnative invasive
species; a small population size that
makes both sites susceptible to genetic
drift and inbreeding; and the potential
for hybridization with two other species
of Artemisia. Ongoing conservation
actions have reduced trampling, but
have not eliminated or reduced the
other threats at the Grant County site.
The magnitude of threat is high for this
variety because the only two remaining
populations are widely separated and
distributed such that one or both
populations could be eliminated by a
single disturbance. The threats are
imminent because recreational use is
ongoing, invasive nonnative species
occur at both sites, erosion of the
substrate is ongoing at the Klickitat
County site, and high water flows are
random, naturally occurring events that
may occur unpredictably in any year.
Therefore, we retained a listing priority
number of 3 for this plant variety.
`
Astelia waialealae (Paainiu)—The
following summary is based on
information contained in our files. No
new information was provided in the
petition received on May 11, 2004.
`
Paianiu is a perennial herb found in
Metrosideros polymorpha (ohia)
dominated mixed montane bog on
Kauai, Hawaii. Astelia waialealae is
known from three populations in three
bogs within the Alakai swamp region of
Kauai. The total numbers have declined
from 35 clumps, representing 10 to 15
genetically distinct individuals, in 2004
to 21 clumps in 2005, representing 7
genetically distinct individuals. No
regeneration has been observed from
1995 to the present. The major threats
to this species currently are the lack of
regeneration and the low numbers of
individuals. The species is also
threatened by pigs that eat and trample
this plant and its seedlings, degrade
and/or destroy habitat, and spread the
nonnative plant species Juncus
planifolius and Andropogon virginicus
that compete with A. waialealae. Pigs
have been fenced out of the three bogs
where A. waialealae currently occurs
and nonnative plant control is
underway; however, this species is not
recovering and continues to decline,
even though the known threats of feral
pigs and nonnative plants have been
controlled over the past nine years. The
threats continue to be of a high
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magnitude because of small population
size and range make it extremely
vulnerable, and efforts to address the
threats have not halted the decline. In
addition, the threats are imminent
because they are ongoing as evidenced
by the continuing decline of the species.
Therefore, we retained a listing priority
number of 2 for this species.
Astragalus tortipes (Sleeping Ute
milkvetch)—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 amplectens (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. This
species is an erect perennial or
facultatively annual herb found in
mixed lowland dry shrubland/grassland
on Oahu, Hawaii. Known from one
population of 500 to 1,000 individuals
in the Waianae Mountains, the threats to
this species are nonnative plants that
increase the fuel load and fire threat,
and compete for habitat. The magnitude
of threats continues to be high because
no conservation measures have been
taken to address them and because of
the potential for the elimination of the
only known population by a single
stochastic or naturally occurring event.
Threats continue to be imminent
because they are ongoing. We retained
a listing priority number of 2 for this
species.
Bidens campylotheca ssp. pentamera
(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. This subspecies is an
erect, perennial herb found in
Cheirodendron-Metrosideros
polymorpha (olapa-ohia) montane wet
forest on Maui, Hawaii. This subspecies
is known from 11 populations with a
total of approximately 500 individuals.
Bidens campylotheca ssp. pentamera is
threatened by feral pigs that degrade
and destroy habitat, and by nonnative
plants that compete for habitat. Feral
pigs have been fenced out of three of the
11 populations of B. campylotheca ssp.
pentamera and nonnative plants have
been greatly reduced in the three fenced
areas. This subspecies is represented in
an ex-situ collection and reintroduction
or augmentation efforts have been
attempted this year. However, these ongoing conservation efforts benefit only
three of the 11 known populations and
therefore threats continue to be of a high
magnitude to this subspecies. In
addition, threats to B. campylotheca
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ssp. pentamera are imminent because
they are ongoing in eight of the 11
populations. Therefore, we retained a
listing priority number of 3 for this
subspecies.
Bidens campylotheca ssp. waihoiensis
(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 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.
Bidens conjuncta is an erect, perennial
herb found in MetrosiderosDicranopteris (ohia-uluhe) lowland to
montane wet forest and shrubland on
Maui, Hawaii. Seven populations are
known, and the number of individuals
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 individuals has declined over
the last decade or so. This species is
threatened by pigs that degrade and
destroy habitat, and eat vegetative parts
and fruit of B. conjuncta, and by
nonnative plants that outcompete and
displace it. Feral pigs have been fenced
out of about half of the populations of
B. conjuncta, and nonnative plants have
been greatly reduced in the fenced
areas. The threats from feral pigs and
nonnative plants are, therefore, of a
moderate magnitude to this species
because they impact only about half of
its populations. In addition, these
threats are imminent because they are
ongoing in half of the populations.
Therefore, we retained a listing priority
number of 8 for this species.
Bidens micrantha ssp. ctenophylla
(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. This subspecies is an
erect, perennial herb found in open
mixed shrubland to dry Metrosideros
(ohia) forest on the island of Hawaii,
Hawaii. This subspecies is endemic to
the island of Hawaii, where it is
restricted to an area of less than 10
square miles (26 square kilometers).
Bidens micrantha ssp. ctenophylla is
known from four populations totaling
approximately 3,000 individuals, the
majority of which occur in only two
populations. This subspecies is
threatened by fire and nonnative plants,
such as Pennisetum setaceum (fountain
grass) and Leucaena leucocephala (koa
haole), and two populations are
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threatened by residential and
commercial development. The threats to
B. micrantha ssp. ctenophylla from fire
and nonnative plants are of a high
magnitude and imminent because they
are occurring range-wide and no efforts
for their control have been undertaken.
In addition, two populations are also
threatened by development. Therefore,
we retained a listing priority number of
3 for this subspecies.
Brickellia mosieri (Florida brickellbush)—The following summary is based
on information contained in our files.
No new information was provided in
the petition received on May 11, 2004.
This species is restricted to pine
rocklands of Miami-Dade County,
Florida. This habitat requires periodic
prescribed fires to maintain the low
understory and prevent encroachment
by native tropical hardwoods and some
exotic pest plants, such as Brazilian
pepper. Only one large population (up
to 10,000 individuals) is known to exist,
plus 16 other populations that do not
each exceed 100 individuals. There is
little likelihood of finding additional
populations because less than one
percent of the original pineland habitat
still exists and this habitat has been
mapped and surveyed for rare plants
over the past two years. Throughout its
range, this species is threatened by
exotic pest plants and conversion of
pinelands to other uses. New exotic pest
plants are expected to invade pine
rocklands, even as effective control
methods are found for existing pests.
However, 15 of the 17 sites are on
conservation lands where control of
invasive species is being implemented
and controlled burns are being
conducted. In the limited area of
protected conservation lands it is
difficult to conduct prescribed fires in
urban areas. Nonnative plant species
also pose a threat and are difficult to
control. Thus, the overall magnitude of
threat is moderate. The threats are
ongoing and thus imminent. We
assigned this species a listing priority
number of 8.
Calamagrostis expansa (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. This species is a robust, shortrhizomatous perennial found in wet
forest, open bogs, and bog margins on
the islands of Maui and Hawaii, Hawaii.
Historically rare, C. expansa was
restricted to wet forest and bogs on
Maui. It is unknown what the historical
status was on Hawaii. Currently, this
species is known from 100 populations
totaling approximately 400 individuals
on Maui, and was recently discovered in
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five populations totaling approximately
300 individuals on the island of Hawaii.
Calamagrostis expansa is threatened by
pigs that degrade and destroy habitat
and by nonnative plants that
outcompete and displace it. Feral pigs
have been fenced out of most of the west
Maui populations where C. expansa
currently occurs and nonnative plants
have been reduced in the fenced areas.
However, the threats are not controlled
and are ongoing in the remaining
unfenced populations on Maui and in
all of the populations on the island of
Hawaii. Therefore, the threats from feral
pigs and nonnative plants are of a high
magnitude and imminent for C.
expansa, and we retained a listing
priority number of 2 for this species.
Calamagrostis hillebrandii (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.
Calamagrostis hillebrandii is a slender,
short-rhizomatous perennial found in
Metrosideros-Machaerina montane wet
bog or Metrosideros-RhynchosporaOreobolus mixed bog on Maui, Hawaii.
This species is known from two
populations of about 2,000 individuals,
restricted to the bogs of west Maui,
although it was formerly found on the
island of Molokai as well. This species
is currently threatened by pigs that
degrade and destroy habitat and
nonnative plants that outcompete and
displace it. An ungulate exclosure fence
has been constructed and another one is
under construction to protect both
populations of this species, and
nonnative plants are being reduced in
the fenced area. We retained a listing
priority number of 2 for this species
because the threats are ongoing in one
of the two known populations and so
are imminent and of a high magnitude.
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 a spiny,
leguminous shrub currently known from
´
only two localities within the Susua
Commonwealth Forest in the
municipalities of Yauco and Sabana
Grande, in southwestern Puerto Rico.
Twenty-five native species of Calliandra
have been reported for the Antilles;
three are native to Puerto Rico,
including C. locoensis. This species is
endemic to Puerto Rico, and was
discovered in 1991 during a study of the
´
flora of the Susua Commonwealth
Forest. It was described by Garca and
Kolterman in 1992.
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Calliandra locoensis is found at two
locations along one creek in semievergreen to deciduous forests on
shallow, serpentine soils with low
nutrients, high drainage, and low
fertility. Much of the vegetation in the
forest was cut for wood, cultivation,
livestock grazing, and charcoal
production, prior to its designation as a
public forest. Calliandra locoensis
exhibits low degree of self-compatibility
in pollination tests. Seeds have short
viability period, do not appear to have
a biotic dispersal agent (dispersed by
dehiscence), and require mesic
conditions for germination, which may
be factors in the species’ limited
distribution. The small number of
individuals, restricted distribution (two
localities), forest management practices
(accidental trampling, brush clearing,
trail maintenance), forest fires (natural
or manmade), and catastrophic natural
events (hurricanes, floods, mudslides),
threaten this species. We assign a listing
priority number of 5 to this species
because the magnitude of threat to C.
locoensis is high, due to its restricted
distribution, apparent low dispersal
capability, and population number (only
two small populations relatively close to
one another). The threats are
nonimminent given that the populations
are found within protected lands and
there are no known projects or
management activities planned that
would destroy the known populations
of C. locoensis.
Calochortus persistens (Siskiyou
mariposa lily)—The following summary
is based on information contained in
our files and the petition received on
September 10, 2001. 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
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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.
Because of the restricted range and low
numbers, the magnitude of threats is
high. While some of the threats are
ongoing, others are not and overall, the
threats are nonimminent. We assigned a
listing priority number of 5 to this
species.
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. Calyptranthes
estremerae was only known from
several individuals found near the
recreation area adjacent to the Camuy
Caves, but specimens were later found
´
within the Rıo Abajo Commonwealth
´
Forest. Within the Rıo Abajo Forest area,
C. estremerae was known to be located
´
within the protected area of the Rıo
Abajo Commonwealth Forest and at a
site that was impacted by the
construction of state road PR–10. In
1999, four small specimens of C.
estremerae were affected by the road
construction, and an additional
specimen was transplanted to the Puerto
Rico Department of Natural and
Environmental Resources nursery in the
´
Rıo Abajo Forest. Additional specimens
of C. estremerae, later found during
plant surveys that were part of the
mitigation for the construction of PR–
10, were successfully transplanted
within the forest boundaries, to prevent
their destruction during construction of
the road. A minimum of 100 specimens
of C. estremerae are estimated for the
´
Rıo Abajo Commonwealth Forest. The
magnitude of threat to C. estremerae is
high, due to the small number of
individuals in the two populations, the
species’ limited distribution, the species
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vulnerability to catastrophic natural
events, and the potential destruction of
specimens from expansion of
recreational facilities. However, these
threats are not imminent because the
largest known population of C.
estremerae is found within protected
lands, there are no known projects
planned that would destroy the sites,
and the species can be transplanted
successfully. Therefore, we assign a
listing priority number of 5 to this
species.
Canavalia napaliensis (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. 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
threatened by goats that degrade and
destroy habitat, and by nonnative plants
that outcompete and displace it. There
are no conservation measures underway
to alleviate these ongoing, or imminent,
threats to C. napaliensis. These threats
are of a high magnitude because they are
occurring throughout its limited range.
Therefore, we retained a listing priority
number of 2 for this species because the
threats continue to be of a high
magnitude and are imminent in all three
populations.
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 at least 10 populations
totaling less than 200 individuals. This
species is threatened by development
(Maui), goats that degrade and destroy
habitat (Kauai and Maui), and by
nonnative plants that outcompete and
displace native plants (all islands). Feral
goats have been fenced out of three of
the ten populations where C. pubescens
currently occurs and nonnative plants
have been reduced in two of the
populations that are fenced. This
species is represented in an ex situ
collection. Because the threats are
ongoing in more than half of the known
populations they are of a high
magnitude and imminent. Therefore, we
retained a listing priority number of 2
for this species.
Castilleja christii (Christ’s
paintbrush)—See above in ‘‘Summary of
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Listing Priority Changes in Candidates.’’
The above summary is based on
information contained in our files and
the petition received on January 2, 2001.
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).
In recent decades, its known
distribution was restricted to Big Pine
Key, until a population was found on
Lower Sugarloaf Key in 2005. Roughly
90 percent of its current range is within
the Service’s 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) of Big Pine Key. Pine
rockland communities are maintained
by relatively frequent fires. The most
vigorous populations of this species are
located in areas that have burned within
a decade. In the absence of fire, woody
encroachment ensues, and the pea is
shaded out. Lack of fire poses the
greatest threat to the pea. The Refuge
has an active prescribed fire program,
though with many constraints. We do
not have new information on
populations, and relevant recent
research is pending publication. We are
maintaining the previous assessment
that a very narrow distribution,
combined with sea level rise as well as
fire management and exotic pest plant
threats, makes for an overall high
magnitude of threat. We maintain that
the immediacy of threats is
nonimminent, because a significant
portion of the range is in conservation
lands wherein threats are substantially
controlled. Sea level rise remains
uncontrolled, but is nonimminent
regarding most of the habitat area or
population on an annual basis.
Accordingly, we assigned the Big Pine
partridge pea a listing priority number
of 6.
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
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in the petition received on May 11,
2004. Wedge spurge is a small prostrate
herb, forming patches among 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 and 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 short-term
threat, although sea level rise is
ultimately a threat of equal or greater
magnitude. The National Key Deer
Refuge has an active prescribed fire
program, though with many constraints.
We do not have new information on
populations, although an abundance
and distribution survey is under way.
We maintain the previous assessment
that a very narrow distribution
composed of small sub-populations
results in a high magnitude of threat.
Specific threats include fire
suppression, invasive exotic plants, sea
level rise, and stochastic threats related
to small population size, including
hurricanes. The immediacy of threats is
nonimminent because a significant
portion of the range is on conservation
lands wherein threats are substantially
controlled. Sea level rise remains
uncontrolled, but is nonimminent
regarding most of the habitat area or
population on an annual basis.
Therefore, we retained a listing priority
number of 6 for wedge spurge.
Chamaesyce eleanoriae (Akoko)—The
following summary is based on
information contained in our files. No
new information was provided in the
petition received on May 11, 2004. This
species is a small shrub found in steep
slopes and cliffs, in MetrosiderosDiospyros lowland mesic forest, and
Eragrostis variabilis coastal dry cliffs on
Kauai, Hawaii. This species has
declined from 10 populations totaling
500 individuals in 1996 to three
populations totaling less than 50
individuals, found only in and around
Kalalau Valley rim, along the Na Pali
Coast on the island of Kauai.
Chamaesyce eleanoriae is threatened by
goats that eat it, degrade and destroy
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habitat, by nonnative plants that
outcompete and displace it, and by
stochastic extinction due to naturally
occurring events. Chamaesyce
eleanoriae is also potentially threatened
by rats that eat it. All of the threats
occur range-wide and no efforts to
control goats, rats, and nonnative plants
have been undertaken. The threats are of
a high magnitude because of their
severity and because they occur rangewide. The threats are ongoing and
therefore imminent. We retained a
listing priority number of 2 for this
species.
Chamaesyce remyi var. kauaiensis
(Akoko)—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 variety is a shrub found in
wind-swept shrubland and adjacent
forest patches dominated by
Metrosideros (ohia) and Syzygium on
Kauai, Hawaii. Chamaesyce remyi var.
kauaiensis is known from 5 populations
totaling 800 to 1,000 individuals. This
variety is found only in the Blue Hole,
Lumahai Valley, Wainiha, and Iliiliula
areas on the island of Kauai. Threats to
C. remyi var. kauaiensis include goats
and pigs that degrade and destroy
habitat, the two-spotted leafhopper that
damages leaves and may spread plant
viruses, and nonnative plants that
outcompete and displace it. There are
no conservation measures being taken to
alleviate these threats to C. remyi var.
kauaiensis. The threats are of a high
magnitude because of their severity and
because goats and pigs, the two-spotted
leafhopper, and nonnative plants are
found throughout the shrubland and
forest areas C. remyi var. kauaiensis
occurs in. The threats are ongoing and
therefore imminent. We retained a
listing priority number of 3 for this
variety.
Chamaesyce remyi var. remyi
(Akoko)—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 variety is a perennial shrub
found in wet Metrosideros polymorphaDicranopteris 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
variety is threatened by goats and pigs
that degrade and destroy habitat and
potentially eat this plant, by the twospotted leafhopper that causes leaf
damage and may spread viruses, and by
nonnative plants that outcompete and
displace it. Feral pigs and goats have
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been fenced out of two of the ten
populations of C. remyi var. remyi, and
nonnative plants have been reduced in
the two fenced areas. Although two of
the ten populations of this variety have
been fenced and are undergoing weed
control, there are no efforts to control
the ongoing threats to the other eight
populations. The threats are of a high
magnitude because of their severity and
are imminent because they are ongoing
in eight of the ten known populations.
We retained a listing priority number of
3 for this variety.
Charpentiera densiflora (Papala)—
The following summary is based on
information contained in our files. No
new information was provided in the
petition received on May 11, 2004. This
species is a tree found in Diospyros
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
kilometers) in the Na Pali coast area on
the island of Kauai. This species is
threatened by goats that degrade and
destroy habitat, flooding, and nonnative
plants. Feral goats have been fenced out
of one of the 10 populations where C.
densiflora currently occurs, and
nonnative plants are being controlled in
the fenced area. This species is
represented in an ex situ collection. The
threat from flooding is of high
magnitude and imminent because no
flood control measures have been
undertaken for any of the populations.
The threats from goats and nonnative
plants occur in nine of the ten known
populations and are, therefore,
imminent. The threats are also of a high
magnitude because of their severity in
the nine populations. Therefore, we
retained a listing priority number of 2
for this species.
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. Chorizanthe parryi var.
fernandina is a low growing herbaceous
annual plant in the buckwheat family.
Germination occurs following the onset
of late-fall and winter rains and
typically represents different cohorts
from the seed bank. Flowering occurs in
the spring, generally between April and
June. Chorizanthe parryi var. fernandina
grows up to 30 centimeters in height
and 5 to 40 centimeters across.
The plant currently is known from
two disjunct localities: The first is in the
southeastern portion of Ventura County
on a site formerly known as Ahmanson
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Ranch, and the second is in an area of
southwestern Los Angeles County
known as Newhall Ranch. Investigations
of historical locations and seemingly
suitable habitat within the range of the
species have not revealed any other
occurrences.
The threats currently facing San
Fernando Valley spineflower include
threatened destruction, modification, or
curtailment of its habitat or range, and
other natural or manmade factors. The
threats to C. parryi var. fernandina from
habitat destruction or modification are
less than they were two years ago. One
of the two populations (Ahmanson
Ranch) is in permanent, public
ownership and is being managed by an
agency that is working to conserve the
plant. The other population (Newhall
Ranch) is under threat of development;
however, a Candidate Conservation
Agreement with Assurances (CCAA) is
being developed with the landowner,
and it is possible that the remaining
plants can also be conserved. Until such
an agreement is finalized, the threat of
development and the potential damage
to the Newhall Ranch population still
exists.
Chorizanthe parryi var. fernandina is
particularly vulnerable to extinction due
to its concentration in two isolated
areas. The existence of only two areas of
occurrence, and a relatively small range,
makes the variety highly susceptible to
extinction or extirpation from a
significant portion of its range due to
random events such as fire, drought,
erosion, or other events. We retained a
listing priority number of 6 for C. parryi
var. fernandina due to high magnitude
of nonimminent threats.
Chromolaena frustrata (Cape Sable
thoroughwort)—The following summary
is based on information contained in
our files. No new information was
provided in the petition received on
May 11, 2004. Chromolaena frustrata is
found most commonly in open sun to
partial shade at the edges of rockland
tropical hammock and in coastal rock
barrens along the northern edges of
Florida Bay in Everglades National Park,
Monroe County, Florida. It is known
from coastal berms along the northern
edges of Florida Bay in Everglades
National Park. It has not been observed
in artificially disturbed areas, but is
abundant in a tropical hammock that
lost some of its tree canopy in a
hurricane. Coastal rock barrens are
composed of exposed Key Largo
Limestone with a diverse assemblage of
salt tolerant herbs. Due to extensive
development, remaining areas of natural
vegetation are limited. Land acquisition
by the State has benefited this species,
as has private land management.
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However, only one large population of
this species is known and its history
suggests that it will decline as the forest
canopy recovers. With so few
populations in existence (seven), it is
not likely that the species will persist.
These factors, combined with the threat
from invasive exotic pest plants,
constitute a high magnitude of threat.
We anticipate that land managers will
address exotic pest plant threats as
funding is available. The conservation
situation on the privately-owned site
with the largest known population is
encouraging. Local extirpations of this
species, due to exotics or other reasons,
can possibly be reversed by
reintroductions. However, we consider
the threats to this narrowly endemic
plant with no really large populations to
be imminent because exotic pest plants
are currently present. As a result, we
assigned a listing priority number of 2
to this species.
Consolea corallicola (Florida
semaphore cactus)—The following
summary is based on information in our
files. No new information was provided
in the petition received on May 11,
2004. The Florida semaphore cactus is
endemic to the Florida Keys and was
discovered on Big Pine Key in 1919 but
has since been extirpated there as a
result of road building and poaching.
This cactus grows close to salt water on
bare rock with a minimum of humussoil cover in or along the edges of
hammocks near sea level. The species is
known to naturally occur only in two
areas, Little Torch Key and Biscayne
National Park. Outplanting has resulted
in the reestablishment of a population
in Dagny Johnson Key Largo Hammock
Botanical State Park in North Key Largo
as well as in some of the lower keys.
Outplanting success has been low and
more research is needed to determine
the requirements of this cacti. Only 5 of
the original 14 mature plants (as well as
new recruits from fallen pads) remain 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 is not possible without human
intervention. Regeneration in this
population is restricted to clonal
propagation. At least 629 plants were
discovered on a key in Biscayne
National Park in November of 2001. A
recent study found no genetic diversity
within the two wild populations. The
results were consistent with previous
reproductive biology studies that
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suggested that the cactus does not
propagate sexually and that asexual
reproduction is the main life-history
strategy of this species. The causes for
the population decline of this species
include destruction or modification of
habitat, predation from Cactoblastis
cactorum moths, poaching, and
hurricanes and other natural disasters.
According to scientists, intervention
will be required if the species is to
survive the next 10 years. Because of
low population numbers, reproductive
problems, and numerous ongoing
threats, we assigned this species a
listing priority number of 2.
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,
Vieques Island, and Anegada in the
British Virgin Islands. The status of the
Anegada population is not known.
Cordia rupicola is known only from dry
forest communities on limestone
substrates at low elevation. The
currently known largest concentration
of C. rupicola in Puerto Rico is found on
˜
privately-owned lands in Penuelas
where extensive land clearing for
residential lots continues to take place.
We assigned a listing priority number of
2 to C. rupicola because the magnitude
of threat to this species is high due to
its restricted distribution, low
population number (not more than 25
known specimens), urban expansion,
maintenance of electrical facilities, and
catastrophic natural events that threaten
the Puerto Rico population, and the
threats to C. rupicola are imminent,
since only a small fraction of the
species’ known population falls within
protected lands, and the largest
concentration is found in privatelyowned land subjected to urban
expansion.
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. Currently, this species is known
from 4 populations totaling less than
200 individuals. Cyanea asplenifolia is
threatened by pigs and goats that
degrade and destroy habitat and by
nonnative plants, such as Australian
tree fern, that outcompete and displace
it. Potential threats to this species
include rats and slugs that may directly
prey upon and defoliate individuals. Pig
and goat exclusion fences protect two of
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the four known populations of this
species and nonnative plants have been
reduced in the fenced areas. This
species is represented in an ex-situ
collection. The threats continue to be of
a high magnitude and imminent because
no conservation efforts are being taken
to address them and they are ongoing in
two of the four known populations.
Therefore, we retained a listing priority
number of 2 for this species because the
threats are of a high magnitude and are
imminent since they are ongoing.
Cyanea calycina (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. This
species is an unbranched shrub found in
Metrosideros-Dicranopteris montane
wet forest and wet gulches and
streambanks on Oahu, Hawaii. Cyanea
calycina is known from about 20
populations with a combined total of
200 or more individuals. This species is
threatened by pigs and goats that
degrade and destroy habitat, and by
nonnative plants that outcompete and
displace it. Potential threats to this
species include rats and slugs that may
directly prey upon and defoliate
individuals. There are no conservation
measures underway to alleviate these
ongoing, or imminent, threats to C.
calycina. These threats are of a high
magnitude because they are occurring
throughout its limited range. Therefore,
we retained a listing priority number of
2 for this species because the threats
continue to be of a high magnitude and
are imminent in all populations.
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, and
only ever known from one population
totaling less than ten individuals in
Wainiha Valley on Kauai. In 2005, we
received information that there are no
extant wild individuals and there is no
material in genetic storage. This species
was likely highly threatened by pigs that
degrade and destroy habitat, by rats and
slugs that may have consumed it, and by
nonnative plants that likely
outcompeted and displaced it. We are
considering removing this species from
candidate status since it appears to be
extinct. However, we are seeking any
new information that indicates this
species is still extant and will reevaluate the status of this species in the
coming year.
Cyanea kuhihewa (Haha)—The
following summary is based on
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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 (ohia-uluhe) lowland wet forest
on Kauai, Hawaii. This species was only
ever known from one population
totaling six individuals in Limahuli
Valley on Kauai. 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. Currently, C.
kuhihewa is represented only in an exsitu collection. This species is
threatened by pigs that degrade and
destroy habitat, by rats and slugs that
that may directly prey upon and
defoliate it, and by nonnative plants that
outcompete and displace it. The only
known location for this species has been
protected by fences and nonnative
plants have been reduced in the fenced
area. Currently, no individuals have
been reintroduced into this site. In
addition, no control measures have been
implemented in this site to address the
threats from rats and slugs. Because of
these factors, we retained a listing
priority number of 2 for this species.
Cyanea kunthiana (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 kunthiana is a shrub found in
closed Metrosideros polymorpha
montane wet forest on Maui, Hawaii.
The historic range of C. kunthiana was
wet forest on the island of Maui.
Currently, C. kunthiana is declining
throughout its range and is known from
approximately 20 populations with a
combined total of several hundred
individuals. This species is threatened
by pigs that directly prey upon the
plants and degrade and destroy habitat,
and by nonnative plants that
outcompete and displace it. Potential
threats to this species include rats and
slugs that may directly prey upon and
defoliate individuals. Feral pigs have
been fenced out of three of the 20
populations of C. kunthiana and
removal of feral pigs from fenced areas
is on-going. Control of nonnative plants
in the three fenced areas is underway.
Although three of the 20 populations of
C. kunthiana have been fenced and are
undergoing weed control, there are no
efforts to control the ongoing and
imminent threats to the other 17
populations. Therefore, the threats
continue to be of a high magnitude to
C. kunthiana. Because the threats
continue to be of a high magnitude and
are imminent for 17 of the 20
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populations, we retained a listing
priority number of 2 for this species.
Cyanea lanceolata (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 lanceolata is a shrub found in
Acacia koa-Metrosideros polymorpha
(koa-ohia) lowland mesic forest on
Oahu, Hawaii. This species is known
from 20 populations totaling less than
300 individuals. Cyanea lanceolata is
threatened by pigs, that eat plants and
degrade and destroy habitat, and by
nonnative plants that outcompete and
displace it. Potential threats to this
species include rats and slugs that may
directly prey upon and defoliate
individuals. There are no conservation
measures underway to alleviate these
ongoing, or imminent, threats to C.
lanceolata. These threats are of a high
magnitude because they are occurring
throughout its limited range and are
imminent in all populations. Therefore,
we retained a listing priority number of
2 for this species.
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 (ohia) mixed
mesic forest on Maui, Hawaii. This
species is known from six populations
with a combined total of approximately
30 individuals. Cyanea obtusa is
threatened by feral goats, pigs, and
cattle that degrade and destroy habitat,
and by nonnative plants that
outcompete and displace it. Potential
threats include rats and slugs that may
directly prey upon and defoliate
individuals of C. obtusa. Feral ungulates
have been fenced out of one of the six
populations of this species, and another
fence is under construction to protect a
second population. Nonnative plant
control is underway in the fenced
population and will be initiated in the
second fenced population once the
fence is completed. Although one of the
six populations of C. obtusa has been
fenced and is undergoing weed control,
and fencing of a second population is
underway, there are no efforts to control
the ongoing and imminent threats to the
other four populations. Therefore, the
threats continue to be of a high
magnitude for C. obtusa. Because the
threats continue to be of a high
magnitude and are imminent for four of
the six known populations, we retained
a listing priority number of 2 for this
species.
Cyanea tritomantha (Aku)—The
following summary is based on
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information contained in our files. No
new information was provided in the
petition received on May 11, 2004.
Cyanea tritomantha 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.
Cyanea tritomantha is threatened by
pigs that degrade and destroy habitat,
and nonnative plants that outcompete
and displace it. Potential threats to this
species include rats and slugs that may
directly prey upon and defoliate
individuals, and human trampling of
individuals located near trails. Feral
pigs have been fenced out of two
populations of C. tritomantha and
nonnative plants have been reduced in
the fenced areas. Although two
populations of C. tritomantha have been
fenced and weeds are being controlled
in these fenced areas, there are no
efforts to control the ongoing and
imminent threats to the other
populations. Therefore, the threats
continue to be of a high magnitude to
C. tritomantha. Because the threats
continue to be of a high magnitude and
are imminent for the unmanaged
populations, we retained a listing
priority number of 2 for this species.
Cyrtandra filipes (Haiwale)—The
following summary is based on
information contained in our files. No
new information was provided in the
petition received on May 11, 2004.
Haiwale is a shrub found in lowland
wet and mesic forest on Maui and
Molokai, Hawaii. Historically rare, C.
filipes was 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 true identity of the Maui
populations, which do not fit the
description of the species precisely. If,
upon further taxonomic study, the Maui
populations are determined not to be
this species, then it is even rarer, with
only the Molokai population of a few
individuals remaining. Cyrtandra filipes
is threatened by pigs and deer that
degrade and destroy habitat, by
nonnative plants that outcompete and
displace it and potentially by rats that
directly prey on it. Feral pigs have been
fenced out of one of the three
populations of C. filipes but deer are
able to jump over most pig exclusion
fences so they are still considered a
threat. Nonnative plants are being
reduced in the population that is fenced
but all populations are potentially
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threatened by rats. The threat from deer
is of a high magnitude and imminent
because no deer control measures have
been undertaken for any of the
populations. The threats from pigs and
nonnative plants occur in two of the
three known populations and are,
therefore, of a high magnitude because
of their severity. In addition, these
threats are imminent because they are
ongoing. Therefore, we retained a listing
priority number of 2 for this species.
Cyrtandra kaulantha (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 kaulantha 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
23 individuals along the Waiahole Ditch
Trail. Cyrtandra kaulantha is threatened
by pigs that degrade and destroy habitat,
by nonnative plants that outcompete
and displace it, genetic bottlenecks,
random demographic fluctuations, and
stochastic environmental events such as
tree falls and hurricanes. Direct
predation by slugs is a potential threat.
None of the populations are protected
by fences. Nonnative plants have been
reduced in only one of the seven known
populations. There are no other
conservation measures being taken to
alleviate these ongoing and imminent
threats to C. kaulantha. These threats
are of a high magnitude because of their
severity and they are occurring
throughout its limited range. Therefore,
we retained a listing priority number of
2 for this species because the threats
continue to be of a high magnitude and
are imminent in all populations.
Cyrtandra oenobarba (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 oenobarba is a low,
decumbent, fleshy, subshrub found in
Metrosideros polymorpha-Dicranopteris
linearis (ohia-uluhe) lowland wet forest
on Kauai, Hawaii. The historic range of
this species was throughout the island
of Kauai. Recent surveys show that the
species is now limited to 10 or more
populations totaling 200 to 500
individuals in only three small areas on
the island of Kauai. Cyrtandra
oenobarba is threatened by pigs that
degrade and destroy habitat, and by and
nonnative plants that outcompete and
displace it. There are no conservation
measures being taken to alleviate these
threats to C. oenobarba. Pigs and
nonnative plants are found throughout
the lowland wet forest habitat of this
species, and, therefore, are ongoing and
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imminent. In addition, the threats are of
a high magnitude because of their
severity and because they occur
throughout the limited range of this
species. Because the threats are of a high
magnitude and are imminent in all
known populations, we retained a
listing priority number of 2 for this
species.
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 (ohia-olapa)
montane wet forest to mesic AcaciaMetrosideros (koa-ohia) forest on Maui,
Hawaii. Currently, this species is known
only from one population totaling 250 to
300 individuals in the Kahikinui area of
east Maui and one additional
population of 25 individuals on west
Maui. This species is threatened by pigs
that degrade and destroy habitat, and by
nonnative plants that outcompete and
displace it. Feral pigs have been fenced
out of the smaller of the two
populations of C. oxybapha, and
nonnative plants have been reduced in
the fenced population. However, the
threats are not controlled and are
ongoing in the remaining, larger
unfenced population. Therefore, the
threats from pigs and nonnative plants
are of a high magnitude and imminent
for C. oxybapha and we retained 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. Cyrtrandra sessilis is
threatened by pigs that degrade and or
destroy habitat, and by nonnative plants
that outcompete and displace it. No onthe-ground conservation efforts have
been initiated but this species is
represented in an ex-situ collection. Pigs
and nonnative plants are found
throughout the mesic and wet forest
habitat in which C. sessilis occurs
making these threats ongoing and
imminent. These threats are of high
magnitude because of their severity and
because they are occurring throughout
its limited range. We retained a listing
priority number of 2 for this species.
Dalea carthagenensis floridana
(Florida prairie-clover)—The following
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summary is based on information
contained in our files. No new
information was provided in the
petition received on May 11, 2004. This
plant has recently been found in Big
Cypress National Preserve in Monroe
and Collier Counties, Florida. It is also
known from five small populations in
Miami-Dade County, two on small tracts
of conservation lands. The populations
in Miami-Dade County are vulnerable to
invasion by exotic pest plants and to
lack of prescribed fire. The populations
in Big Cypress National Preserve do not
appear to be large, and thus may be
vulnerable to random events, as well as
exotic pest plant invasions, with Old
World climbing fern being the chief
threat. The threats from invasive species
are being controlled to some extent.
Prescribed burns are being conducted
on Miami-Dade conservation lands and
biological control agents are being
developed for Old World climbing fern,
so the overall magnitude of threats is
moderate. Threats to the three of the five
Florida prairie-clover populations in
Miami-Dade County are imminent.
Threats from lack of fire and invasive
species are ongoing, and conducting
prescribed fires in urban areas is
difficult, as is controlling exotic pest
plants. The urban conservation lands
where this plant occurs require regular
maintenance. Threats from exotic pest
plants to the two populations in Big
Cypress National Preserve may be
nonimminent because Old World
climbing fern has not yet arrived.
Overall, we consider threats to be
imminent, so assigned a listing priority
number of 9 to this subspecies.
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 two sites in New Jersey,
one site in Delaware, and two sites in
North Carolina. While all five extant D.
hirstii populations are located on public
land or privately owned conservation
lands, natural threats to the species from
encroaching vegetation and fluctuations
in climatic conditions remain of
concern and may be exacerbated by
anthropomorphic factors occurring
adjacent to the species’ wetland habitat.
Given the low numbers of plants found
at each site, even minor changes in the
species’ habitat could result in local
extirpation. Loss of any known sites
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could result in a serious contraction of
the species range. However, the most
immediate and severe of the threats to
this species (i.e., ditching of the
Labounsky Pond site, and encroachment
of aggressive vegetative competitors)
have been curtailed or are being actively
managed by The Nature Conservancy at
the one 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 retained 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
grass occurs at the edges of marl prairies
within pine rocklands of the Long Pine
Key area of Everglades National Park, an
area of about 8,000 hectares (31 square
miles). Because this plant has a narrow
distribution and habitat requirements
and only occurs within the Long Pine
Key area, threats from exotic pest plants
or other habitat management problems
are significant. The National Park
Service has controlled exotic pest plants
and maintains an appropriate fire
regime, but threats remain, particularly
from Old World climbing fern, which is
rapidly spreading into southern Florida
and cannot easily be controlled.
Therefore the magnitude of threats is
high. Because the Old World climbing
fern and perhaps other new exotic pest
plants are not in the immediate vicinity
of D. pauciflora but are expected to
arrive within the next decade, the
threats are nonimminent and the listing
priority number is 5.
Dubautia imbricata ssp. imbricata
(Naenae)—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 subspecies is a shrub found
in wet forest and bogs on Kauai, Hawaii.
Dubautia imbricata ssp. imbricata is
known from three populations totaling
1,000 or more individuals in the
Wahiawa Mountains. This subspecies is
threatened by pigs that degrade and
destroy habitat, and by nonnative plants
that outcompete and displace it.
Nonnative plants have been reduced in
a portion of the species’ range. No other
conservation measures for D. imbricata
ssp. imbricata have been undertaken.
Pigs are found throughout the wet forest
and bog habitat of this subspecies.
Therefore, the threat from pigs is
ongoing and imminent. In addition, the
threat from feral pigs is of a high
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magnitude because the severity of this
threat and because pigs occur
throughout the limited range of this
subspecies. Nonnative plants also
remain a high magnitude threat to D.
imbricata ssp. imbricata because of the
severity of the threat and because they
occur throughout its limited range.
Competition by nonnative plants is an
ongoing and imminent threat to most of
the individuals of D. imbricata ssp.
imbricata, although weed control has
been undertaken in a portion of its
range. We retained a listing priority
number of 3 for this subspecies.
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,
2004. Dubautia plantaginea ssp.
magnifolia is a shrub found in bogs and
wet forest on Kauai, Hawaii. This
subspecies is known from two
populations totaling 100 individuals
near the summit of Waialeale on the
island of Kauai. Dubautia plantaginea
ssp. magnifolia is threatened by pigs
that degrade and destroy habitat,
nonnative plants that outcompete and
displace it, and by stochastic extinction
due to naturally occurring events. Feral
pigs have been fenced out of one of the
two populations of D. plantaginea ssp.
magnifolia, and nonnative plants have
been reduced in the fenced population.
Because of the severity of the threats
and because they are ongoing in one of
the two known populations they are of
a high magnitude and imminent. We
retained a listing priority number of 3
for this subspecies.
Dubautia waialealae (Naenae)—The
following summary is based on
information contained in our files. No
new information was provided in the
petition received on May 11, 2004.
Dubautia waialealae is a shrub found in
bogs and diverse mesic to wet forest on
Kauai, Hawaii. This species is known
from one population totaling less than
800 individuals near the summit of
Waialeale and one individual at the
opposite end of the Alakai Plateau.
Dubautia waialealae is threatened by
pigs that prey on it and degrade and
destroy habitat, by nonnative plants that
outcompete and displace it, and by
stochastic extinction due to naturally
occurring events. Pigs have been fenced
out of the bog where the one individual
of D. waialealae currently occurs. In
addition, fences protect half of the larger
population, and nonnative plants are
being controlled around these
individuals. However, the threats are
not controlled and are ongoing in half
of the larger population. The threats
from pigs and nonnative plants are of a
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high magnitude and imminent for D.
waialealae, thus, we retained a listing
priority number of 2 for this species.
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, but areas in close
proximity to these known populations
have been altered. Cactus populations
located in the Florence area have not
been monitored and these populations
may be in danger of habitat loss due to
recent urban growth in the area. Urban
development near Ajo, Arizona, as well
as that near Sonoyta, Mexico, is a
significant threat to the Acuna cactus.
Populations of the Acuna cactus within
the Organ Pipe Cactus National
Monument have shown a 50 percent
mortality rate in recent years. The
reason(s) for the mortality are not
known, but continuing drought
conditions are thought to play a role.
The Arizona Plant Law and the
Convention on International Trade in
Endangered Species of Wild Fauna and
Flora provide some protection for the
Acuna cactus. However, illegal
collection is a primary threat to this
cactus variety and has been documented
on the Organ Pipe Cactus National
Monument in the past. While the threats
continue to be of a high magnitude, they
are currently nonimminent. Thus, we
retained a listing priority number of 6
for this cactus variety.
Erigeron lemmonii (Lemmon
fleabane)—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 in July 1975.
Erigeron basalticus (Basalt daisy)—
Erigeron basalticus is a perennial,
herbaceous plant with a taproot and one
to several sprawling stems 10 to 15
centimeters (cm) (4 to 6 inches (in))
long. Erigeron basalticus grows in
crevices in basalt cliffs on canyon walls,
at elevations from 380 to 460 meters
(1,250 to 1,500 feet), along the Yakima
River Canyon and Selah Creek, a
tributary of the Yakima River. It is found
in microsites that are largely devoid of
other vegetation and undergoing
primary succession. As of the most
recent survey in 2000, an estimated over
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12,000 E. basalticus plants exist, with
the population distributed among the
same eight, potentially interbreeding
subpopulations that occupy about 67
hectares (ha) (165 acres (ac)) within the
known distribution of approximately 52
km2 (20 mi2). The overall population
size, both in number of individuals and
total area occupied, remained relatively
stable between 1988 and 1998.
However, the numbers of individuals in
the four smallest subpopulations
decreased substantially between those
survey periods. The cause of the decline
is unknown, yet the threats facing this
species include habitat modification,
overutilization from recreational use in
the areas, and randomly occurring
environmental affects. Surveys
undertaken in 2000 by Washington
Department of Natural Resources staff
report the numbers for all eight subpopulations returning to similar levels
as those reported in 1988. Monitoring by
the University of Washington in 2006
will provide data on the species current
status which will be available for our
next CNOR. Based on nonimminent
threats of moderate magnitude, we
assigned a listing priority number of 11
to 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 buy may include low seed
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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, the magnitude of
threat to Umtanum desert buckwheat is
high and the identified threats are
imminent. Thus, we retained 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 endemic to serpentine
habitat of lower montane forests found
between 1,900 and 4,100 feet. Its
distribution is limited to the Red
Mountain and Little Red Mountain areas
of Mendocino County, California, where
it occupies 50 acres and 900 square feet,
respectively. Occupied habitat at Red
Mountain is scattered over 4 square
miles. The 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 this species is
the potential for surface mining for
chromium and nickel. Virtually the
entire distribution of Red Mountain
buckwheat is either owned by mining
interests, or is covered by existing
mining claims, none of which are
currently active. Surface mining would
destroy habitat suitability for this
species. The species is also believed
threatened by tree and shrub
encroachment into its habitat, in
absence of fire. Given the magnitude
(high) and immediacy (nonimminent) of
the threat to the small, scattered
populations, and its taxonomy (species),
we assigned a listing priority number of
5 to this species.
Festuca hawaiiensis (no common
name)—The following summary is
based on information contained in our
files. No new information was provided
in the petition received on May 11,
2004. This species is a cespitose
(growing in dense, low tufts) annual
found in dry forest on the islands of
Hawaii and Maui, Hawaii. Festuca
hawaiiensis is known from more than
20 populations totaling approximately
1,000 individuals in and around the
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Pohakuloa Training Area on the island
of Hawaii. Historically, this species was
also found on Hualalai and Puu
Huluhulu on Hawaii and possibly
Ulupalakua on Maui, but it no longer
occurs at these sites. Festuca
hawaiiensis is threatened by pigs, goats,
and sheep that degrade and destroy
habitat, by nonnative plants that
outcompete and displace it, and by fire.
Feral pigs, goats, and sheep have been
fenced out of a portion of the
populations of F. hawaiiensis, and
nonnative plants have been reduced in
the fenced areas. However, these threats
are not controlled and are ongoing in
the remaining, unfenced populations. In
addition, the threat from fire is of a high
magnitude and imminent because of the
severity of this threat, it occurs
throughout the range of the species, and
no fire control measures have been
undertaken for any of the populations of
F. hawaiiensis. Since the threats are of
a high magnitude and are imminent for
F. hawaiiensis, we retained a listing
priority number of 2 for this species.
Festuca ligulata (Guadalupe fescue)—
The following summary is based on
information from our files and in the
petition received in 1975. Guadalupe
fescue is a member of the Poaceae (Grass
family). This species is currently only
known from higher elevations in the
Chisos Mountains area in the Big Bend
Area of Texas and adjacent Coahuila,
Mexico. The population in Big Bend
National Park is bisected by a trail and
subject to occasional trampling by
horses and hikers. The magnitude of
threats for Guadalupe fescue is
moderate to low because of population
monitoring, fire management, and trail
operation by the National Park Service.
Threats to the overall population are
nonimminent because of monitoring
and other conservation actions that
address threats to the species. Thus, we
assign a listing priority number of 11 to
this species.
Gardenia remyi (Nanu)—The
following summary is based on
information contained in our files. No
new information was provided in the
petition received on May 11, 2004.
Nanu is a tree found in mesic to wet
forest on islands of Kauai, Molokai,
Maui, and Hawaii, Hawaii. Gardenia
remyi is known from several
populations totaling a few hundred
individuals throughout its range. This
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. This
species is represented in an ex situ
collection. Feral pigs have been fenced
out of the west Maui populations of G.
remyi, and nonnative plants have been
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reduced in those areas. However, these
threats are not controlled and are
ongoing in the remaining, unfenced
populations, and are, therefore, of a high
magnitude and imminent. In addition,
the threat from goats is of a high
magnitude, and ongoing and imminent,
because no goat control measures have
been undertaken for any of the
populations of G. remyi. Therefore, we
retained a listing priority number of 2
for this species.
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, as a
result of more thorough surveys, from
over 2,000 individuals. Geranium
hillebrandii is moderately threatened by
pigs that degrade and destroy habitat,
and by nonnative plants that
outcompete and displace it. Feral pigs
have been fenced out of some of the
populations of G. hillebrandii, and
nonnative plants have been reduced in
those areas. The threats from feral pigs
and nonnative plants are, therefore, of a
moderate magnitude to this species
because they affect only about half of its
populations. In addition, these threats
are imminent because they are ongoing
in half of the populations. Therefore, we
retained a listing priority number of 8
for this species.
Geranium kauaiense (Nohoanu)—See
above in ‘‘Summary of Listing Priority
Changes in Candidates.’’ No new
information was provided in the
petition received on May 11, 2004.
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 near Cerro La Santa
in the Carite Commonwealth Forest on
the border of the municipalities of
Cayey and San Lorenzo of southeastern
Puerto Rico. The population previously
reported from the Caribbean national
Forest in Luquillo is apparently no
longer extant. Approximately 172 plants
have been located at the Carite site.
Gonocalyx concolor appears to be
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predominantly outcrossed, and
pollinated by hummingbirds. Successful
propagation at the University of Turabo,
Turabo, Puerto Rico has been achieved.
We assign a listing priority number of 5
to G. concolor, because the magnitude of
threat is high, due to its limited
distribution and population numbers,
prior habitat destruction from
construction of roads and
telecommunication towers, certain
forest management practices,
availability of specific pollinators, and
potential for catastrophic natural events;
the threats to G. concolor are
nonimminent, because the known
population is found within protected
lands, initial efforts at propagation have
been successful, and there are no known
projects or management activities
planned that would destroy the known
population.
Hazardia orcuttii (Orcutt’s
hazardia)—The following summary is
based on information contained in our
files and the petition received on March
8, 2001. Hazarida orcuttii is an
evergreen shrubby species in the
Asteraceae (sunflower family). The
resinous shrubs are 50–100 centimeters
(20–40 inches (in)) high and the
relatively few branches are erect. This
species flowers between August and
October. The only known extant native
occurrence of this species in the U.S. is
in coastal San Diego County, California
at the Manchester Conservation Area,
previously known as the Manchester
Mitigation Bank, now managed by The
Center for Natural Lands Management
(CNLM). The area is about 50 hectares
(ha) (123 acres (ac)) and includes Diegan
coastal sage scrub, southern maritime
chaparral, and willow scrub. Within the
conservation area, the natural
population of H. orcuttii occupies only
2 ha (5 ac). The Manchester
Conservation Area also supports
populations of federally listed California
gnatcatcher (Polioptila californica
californica), Arctostaphylos glandulosa
ssp. crassifolia (Del Mar manzanita),
and Acanthomintha ilicifolia (San Diego
thornmint). The general substrate for the
H. orcuttii is sandstone.
The majority of the native occurrence
has experienced more or less
continuous impacts from people in the
adjacent housing area who use the open
space as a recreation area. Impacts can
include pedestrian trampling and
creation of bicycle trails near H. orcuttii
plants. There are several other existing
and potential threats to this species in
the U.S. Introduced invasive exotic
plants may pose a threat to the
reproductive potential of this species.
Translocations can pose a threat by
removal of plants from viable habitat.
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Removed plants would no longer be a
portion of the extant in-situ population,
thereby affecting the plants genetic and
demographic potential. The loss of
about 147 of the 200 plants translocated
to the Manchester site from an adjacent
native unprotected site represents a loss
of about 29 percent of the known native
plants in the area. This likely represents
a depletion of the genetic diversity of
the species. This species is likely
threatened by low numbers, possibly
low seed set, and seed viability. We are
aware of no reports of seedlings at the
native occurrence. This could be of
considerable consequence and represent
lack of pollinator services and/or
limitations on genetic diversity of an
already small population. We retained a
listing priority number of 5 for H.
orcuttii due to overall nonimminent
threats of high magnitude.
Hedyotis fluviatilis (Kamapuaa)—The
following summary is based on
information contained in our files. No
new information was provided in the
petition received on May 11, 2004.
Kamapuaa 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.
Hedyotis fluviatilis is threatened by pigs
that degrade and destroy habitat, and by
nonnative plants that outcompete and
displace it. All of the threats occur
range-wide and no efforts for their
control or eradication are being
undertaken. We retained a listing
priority number of 2 because the
severity of the threats is high and are
ongoing so are imminent.
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 majority of the Georgia populations
are protected as they are located within
a conservation easement area donated to
The Nature Conservancy by Temple-
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Inland Corporation. We assigned a
listing priority number of 11 to this
species as the magnitude of threats is
moderate since the largest site is under
permanent protection and the threats
are 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.
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 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 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, Ponta site in
Cherokee County; Lovelady in Houston
County; and Highway 94 in Trinity
County, are within highway rights-ofway and are somewhat protected by a
management agreement between Texas
Parks and Wildlife Department and
Texas Department of Transportation.
Because these sites are still vulnerable
to herbicides and adjacent agricultural
activities, they support relatively low
population numbers: Ponta (Highway
204) has ranged from 5 to 0 plants this
year; Lovelady (Highway 230), 3–14
plants; and Highway 94, 15–49 plants.
Continued surveys for H. dasycalyx
have resulted in new populations.
About 300 plants were found on land
owned by the Temple-Inland
Corporation in east Trinity County. A
Candidate Conservation Agreement now
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covers this site, but smaller numbers
have been seen in recent years, possibly
due to changes in the wetland’s
hydrology. Another site discovered on
land previously owned by Champion
International Corporation (near White
Rock Creek in west Trinity County) once
supported 300–400 plants. However, the
status of this population is currently
unknown due to a recent change in
ownership.
In west Houston County, a population
of 300 to 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
discovered in Compartment 55 in Davy
Crockett National Forest at the south
end of Forest Road 503. This population
is large (at least 400), but has not yet
been fully surveyed. Davy Crockett
National Forest represents the only
public land within the range of H.
dasycalyx. 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 (about 200),
but the second has been affected by a
change in hydrology. In 2004, another
200 plants were placed in a third
location, in Compartment 11 of Davy
Crockett National Forest. This site will
be monitored for success in 2006. Two
more sites in Davy Crockett National
Forest have been identified as potential
sites for reintroduction efforts and will
be investigated.
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 has completed a genetic
analysis of H. dasycalyx, confirming it
as a separate species. Stephen F. Austin
State University is continuing a habitat
study of H. dasycalyx and is developing
a high number of plants for
reintroduction purposes. The threats to
the species continue to be of a high
magnitude because of their severity, but
overall are nonimminent. Thus, we
retained a listing priority number of 5
for the Neches River rose-mallow.
Indigofera mucronata keyensis
(Florida indigo)—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
is a rare plant, inherently vulnerable to
extinction because of its limited
numbers. Of the eight populations that
exist, the largest known population is
on private land and comprises up to
1,000 individuals. Seven much smaller
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populations are on conservation lands
in the Florida Keys, Monroe County.
The species’ habitat of coastal rock
barrens, coastal berms, and edges of
tropical hammocks is being invaded by
exotic pest plants. On public
conservation lands, invasive exotic
species are being controlled in some
areas and populations of this species,
although small, have appeared stable in
recent years. Populations on both
private and public lands are subject to
hurricanes, with their subsequent storm
surges. Overall, the threats to this plant
are moderate in magnitude. Because
exotic pest plants, particularly Brazilian
pepper and latherleaf are a chronic
problem, with Brazilian pepper
occupying coastal areas that are not
regularly managed and latherleaf
possibly still increasing, and because
existing populations of this plant are
small, especially on conservation lands,
this species is highly vulnerable to
lapses in habitat management.
Therefore, threats are imminent and the
listing priority number is 9.
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
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
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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 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 are
nonimminent and maintained a LPN of
5.
Joinvillea ascendens ssp. ascendens
(Ohe)—The following summary is based
on information contained in our files.
No new information was provided in
the petition 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
threatened by pigs that degrade and
destroy habitat, by an unknown fungus,
and by nonnative plants that
outcompete and displace native plants.
Feral pigs have been fenced out of some
of the populations of J. ascendens ssp.
ascendens, and nonnative plants have
been reduced in a few populations that
are fenced. However, these threats are
not controlled and are ongoing in the
remaining, unfenced populations. In
addition, an unknown fungus attacks
the seedlings of this subspecies, limiting
regeneration. Most known plants do not
appear healthy. There is no effectively
known control method for this fungus
and no efforts to alleviate its effects are
being implemented for any of the
populations of J. ascendens ssp.
ascendens. The threats to this species
are of high magnitude and are on-going,
and thus are imminent. Therefore, we
retained a listing priority number of 3
for this subspecies.
Keysseria erici (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. 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
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individuals. This species is threatened
by pigs that degrade and destroy habitat,
and by nonnative plants that
outcompete and displace it. Feral pigs
have been fenced out of three of the
bogs where K. erici currently occurs and
nonnative plants have been greatly
reduced in all three fenced bogs.
However, these on-going conservation
efforts benefit only a few of the
populations of K. erici. The majority of
the populations of K. erici are in
unfenced areas and have no protection
from the impacts of pigs and nonnative
plants. Even the three fenced
populations are not secure, due to
funding limitations to support fence
maintenance and weeding that is
needed to prevent incursions of pigs
and nonnative plants. Thus the threats
to this species occur throughout its
range and are particularly significant in
the unfenced areas where a majority of
the populations are located, and are
expected to continue or increase
without control or eradication. Because
the threats are of high magnitude and
ongoing, and therefore imminent, we
retained a listing priority number of 2
for this species.
Keysseria helenae (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. 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. This species is threatened
by pigs that degrade and destroy habitat,
and by nonnative plants that
outcompete and displace it. Feral pigs
have been fenced out of three of the four
bogs where K. helenae currently occurs,
and nonnative plants have been greatly
reduced in all three fenced bogs.
However, without continued monitoring
and maintenance of the fences, pigs
from surrounding areas can easily
access fenced areas. Funding limitations
restrict the extent of such monitoring
and maintenance, and as a result the
fenced populations continue to face
threats. In addition, the threats from
feral pigs and nonnative plants are
ongoing in the unfenced bog. In light of
the low number of individuals of this
species, the threats are of high
magnitude. The threats also are ongoing,
and therefore imminent. For these
reasons, we have retained a listing
number of 2 for this species.
Korthalsella degeneri (Hulumoa)—
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.
Hulumoa is a parasitic subshrub found
on two species of native trees, Sapindus
oahuensis and Nestegis 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. Korthalsella degeneri is
threatened by goats that eat this plant
and degrade and destroy habitat, fire,
and nonnative plants that outcompete
and displace native plants. Goats have
been partially fenced out of the area in
Makua Valley where K. degeneri
currently occurs but some goats are still
present. Fires resulting from military
activities have been minimized but not
completely eliminated. Threats continue
to be of a high magnitude and imminent
because they are ongoing and because of
the potential for the elimination of the
only known population by a single fire
event. Therefore, we retained a listing
priority number of 2 for this species.
Labordia helleri (Kamakahala)—The
following summary is based on
information contained in our files. No
new information was provided in the
petition received on May 11, 2004.
Labordia helleri 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. Labordia helleri is threatened
by goats and deer that eat it and degrade
and destroy habitat, and by nonnative
plants that outcompete and displace it.
No efforts have been taken to control the
threats to L. helleri from goats, deer, and
nonnative plants. The threats are of a
high magnitude and imminent, and
therefore, we retained a listing priority
number of 2 for this species.
Labordia pumila (Kamakahala)—The
following summary is based on
information contained in our files. No
new information was provided in the
petition received on May 11, 2004.
Labordia pumila 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. Labordia
pumila is threatened by pigs that eat it
and degrade and destroy habitat,
nonnative plants that outcompete and
displace it, and by stochastic extinction
due to naturally occurring events such
as hurricanes. Feral pigs have been
fenced out of two of the three bogs
where L. pumila occurs. Nonnative
plants have been greatly reduced in the
two fenced bogs, and are not found in
the immediate vicinity of any L. pumila
individuals in the fenced areas.
Reproduction has not been observed
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over nine years of monitoring, even
within the fenced areas. Also, with only
three known populations, reduced
reproductive vigor and threats from
hurricanes and other stochastic events,
the threats to this species are of a high
magnitude, and are ongoing and
therefore imminent. Consequently, we
retained a listing priority number of 2
for this species.
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 is high for this species, 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 assigned a
listing priority number of 5 to this
species.
Leavenworthia texana (Texas golden
gladecress)—The following summary is
based on information from our files. No
new information was provided in the
petition received on May 11, 2004.
Texas golden gladecress is a small
annual member of the mustard family,
with deep, yellow petals only 7–10
millimeters long; flowering is February
through March. The gladecress occurs
only on the Weches outcrops of east
Texas in San Augustine and Sabine
counties. The Weches geologic
formation consists of a layer of
calcareous sediment that sits above a
layer of glauconite clay. These layers
were deposited up to 50 million years
ago and erosion of the fossil-rich
complex has produced a rugged
topography of steep, flat-topped hills
and escarpments along Highway 21
through north San Augustine and
Sabine Counties. It has also created the
unique ecology of Weches glades:
Islands of thin, loamy, seepy, alkaline
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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. One of
those species is the Texas golden
gladecress which was historically
recorded at eight sites, all in a narrow
line along north San Augustine and
Sabine counties, 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 glauconite
mine was created adjacent to these sites
6 years ago, and may have altered the
area’s hydrology. One historic site in
Sabine County was rediscovered in 1998
and found to support over 300 plants.
Only two known populations remain in
San Augustine County. The Tiger Creek
(Chapel Hill) site is less than 0.1
hectares (less than 0.25 acres) in size
and supports population numbers of
40–100. The Kardell site is less than 9
square meters (100 square feet) in size
and supports 96–490 plants. An
introduced population in Nacogdoches
County has numbered about 300 within
an area of about 18 square meters (200
square feet).
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 threat to
existing gladecress populations is the
invasion of nonnative and weedy shrubs
and vines (primarily Macartney rose
(Rosa bracteata) and Japanese
honeysuckle (Lonicera japonica). All
known sites are undergoing severe
degradation by the incursion of
nonnative shrubs and vines, which
restrict both growth and reproduction of
the gladecress. Special funding allowed
brush clearing to be carried out in 1995
at several white bladderpod sites (where
gladecress is also located). The project
resulted in large increases in white
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
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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 final and in effect)
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 longterm
viability of Weches communities. The
next step is to secure adequate funding
to initiate protection measures.
Landowners of the Tiger Creek 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 retained 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.
Lesquerella globosa is a perennial
member of the mustard family that
occurs in Indiana (1 location), Kentucky
(6 locations), and Tennessee (18
locations). It grows on steep, rocky,
wooded slopes, talus areas, along cliff
tops and bases, and on cliff ledges. It is
usually associated with south to west
facing calcareous outcrops adjacent to
rivers or streams. Road construction and
road maintenance have played a
significant role in the decline of L.
globosa. Specific activities that have
impacted the species in the past and
continue to threaten it include bank
stabilization, herbicide use, mowing
during the growing season, grading of
road shoulders, and road widening or
repaving. Sediment deposition during
road maintenance or from other
activities also potentially threatens the
species. Interruption of natural
processes that maintained habitat
suitability and competition from
invasive nonnative vegetation
necessitates active habitat management
at many locations. Because the threats
would be fatal for populations of this
species, the magnitude of threats is
high. However, based upon the number
of populations and the anticipation that
most of these threats will not be realized
in the several years, the threats are
nonimminent and, therefore, we
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assigned a listing priority number of 5
to 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
herb inhabits seven pine rockland sites
on limestone in Miami-Dade County
and two in the lower Florida Keys (at
National Key Deer Refuge and a Nature
Conservancy preserve on Big Pine Key).
During the twentieth century, most of
this plant’s geographic range was
converted to farmland or was urbanized.
As a result, remaining populations have
suffered from fragmentation and small
population size; only small populations
of this plant remain. Those on relatively
small tracts of conservation land in
urban Miami-Dade County are
vulnerable to invasion by exotic pest
plants and lack of prescribed fire and
such threats could severely affect those
populations. A further problem in
Miami-Dade is that one population is
located in an artificial environment,
which makes its management difficult.
Therefore, the magnitude of threats is
high. The two sites in the Keys seem
less vulnerable to rapid invasions by
exotic pest plants and may require less
frequent prescribed fire because
vegetation grows more slowly there.
Therefore, the threats to the 4 very small
populations are of slightly lesser
magnitude, but they are present. Threats
to four of the seven sand flax
populations in Miami-Dade County are
imminent because they are ongoing. For
the remaining populations, the threats
are less imminent. Overall, the threats
are imminent, and we assigned a listing
priority number of 2 to this species.
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. This plant occupies open, sunny
sites in pinelands of Miami-Dade
County, Florida. Populations with
probably fewer than 100 total
individuals are located on three Countyowned preserves. A population with
more than 100 plants is on a nonconservation site owned by the U.S.
government. The existing populations
are small and vulnerable to exotic pest
plant invasions, hot wildfires, and in
some cases, to development. This
species exists in such small numbers at
so few sites, that it may be difficult to
develop viable populations on the
available conservation lands. Although
no population viability analysis has
been conducted for this plant,
indications are that existing populations
are at best marginal, and none are truly
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viable. As a result, the magnitude of
threats is high. Because no viable
populations of this plant exist, the
imminence of threats is imminent, so
we assigned a listing priority number of
3 to this plant variety.
Lysimachia daphnoides (Lehua
makanoe)—The following summary is
based on information contained in our
files. No new information was provided
in the petition received on May 11,
2004. This species is known from nine
populations totaling 180 to 300
individuals in the Alakai area.
Lysimachia daphnoides is threatened by
feral pigs that degrade and destroy
habitat, by hikers that may trample
individuals, and by nonnative plants
that outcompete and displace it. In
addition, regeneration is not occurring
due to an unknown invertebrate that
eats most, if not all, of the seeds in the
fruit and for which no control is
currently known. Feral pigs have been
fenced out of three of the nine
populations of L. daphnoides and
nonnative plants have been reduced in
the three populations that are fenced.
However, these on-going conservation
efforts benefit only three of the nine
known populations. In addition, no
viable seeds have been observed in
recent years due to damage to fruits
from a boring insect. This insect has not
yet been identified, In monitoring of
populations of L. daphnoides in the
three fenced bogs over the last four
years, no recruitment has been
observed. The threats continue to be of
a high magnitude to the species as a
whole and they are on-going, and
therefore imminent. Therefore, we
retained a listing priority number of 2
for this species.
Melicope christophersenii (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 christophersenii is a long-lived
perennial shrub or tree found in wet
forest in the Waianae Mountains on
Oahu, Hawaii. Currently, this species is
known from several populations totaling
less than 300 individuals. Melicope
christophersenii is threatened by feral
pigs and goats that degrade and destroy
habitat, and nonnative plants that
compete for light and nutrients. The
black twig borer may pose a threat to M.
christophersenii because it is known to
infest other species of Melicope on Oahu
and it occurs throughout the Waianae
Mountains. The threats to M.
christophersenii from feral pigs, goats,
nonnative plants, and the black twig
borer are imminent and of a high
magnitude because of their severity,
they occur range-wide, they are ongoing,
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and no efforts for their control have
been undertaken. Therefore, we retained
a listing priority number of 2 for this
species.
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. Currently this
species is known from three populations
with a total of 15 individuals. Melicope
degeneri is threatened by feral goats that
directly prey upon it and degrade and
destroy habitat, nonnative plants that
compete for light and nutrients, reduced
reproductive vigor, and stochastic
extinction due to naturally occurring
events. The black twig borer may pose
a threat to M. degeneri because it is
known to infest other species of
Melicope and it occurs on the island of
Kauai. No known conservation
measures have been taken to date to
address these threats. These threats are
of a high magnitude because of their
severity and are occurring throughout
the limited range of this species.The
threats are imminent because they are
ongoing in all three populations.
Therefore, we retained a listing priority
number of 2 for M. degeneri.
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 directly prey upon it
and degrade and destroy habitat,
nonnative plants that compete for light
and nutrients, and stochastic extinction
due to naturally occurring events. The
black twig borer may pose a threat to M.
hiiakae because it is known to infest
other species of Melicope on Oahu and
it occurs throughout the Koolau
Mountains. The threats are high in
magnitude and imminent because of
their severity, they all occurring rangewide, and no efforts for their control or
eradication are being undertaken. We
retained 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 in the
Waianae Mountains on Oahu, Hawaii.
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Currently M. makahae is known from
three populations on three discrete
ridges, totaling approximately 200
individuals. This species is threatened
by goats that degrade and destroy
habitat, and nonnative plants that
compete for light and nutrients. The
black twig borer may pose a threat to M.
makahae because it is known to infest
other species of Melicope on Oahu and
it occurs throughout the Waianae
Mountains. The threats to M. makahae
from goats, nonnative plants, and the
black twig borer are of a high magnitude
because of their severity, they are
occurring range-wide, and no efforts for
their control have been undertaken. The
threats are imminent since they are
ongoing. Therefore, we retained a listing
priority number of 2 for this species.
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 (ohia) on
Kauai, Hawaii. Melicope paniculata is
currently known from four populations
totaling 110 individuals. This species is
threatened by feral pigs that directly
prey upon it, degrade and/or destroy
habitat, and nonnative plants that
compete for light and nutrients. The
black twig borer may pose a threat to M.
paniculata because it is known to infest
other species of Melicope and it occurs
on Kauai. All of the threats are
occurring range-wide and no efforts for
their control or eradication are being
undertaken. We retained a listing
priority number of 2 due to imminent
threats of a high magnitude.
Melicope puberula (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 puberula 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. Melicope puberula is threatened
by feral pigs and goats that degrade and/
or destroy habitat, nonnative plants that
compete for light and nutrients, and
stochastic extinction due to naturally
occurring events such as hurricanes.
The black twig borer may pose a threat
to M. puberula because it is known to
infest other species of Melicope and it
occurs on Kauai. These threats are of a
high magnitude because of their severity
and they are occurring throughout its
limited range. The threats are imminent
because they are ongoing. Therefore, we
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retained a listing priority number of 2
for this species.
Myrsine fosbergii (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 fosbergii is a branched shrub or
small tree found in cloud swept 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. Myrsine fosbergii is threatened by
feral pigs that directly prey upon it and
degrade and destroy habitat, and
nonnative plants that compete for light
and nutrients. There are no conservation
measures being taken to alleviate these
threats for this species. Feral pigs are
found throughout the known range of M.
fosbergii making this threat ongoing and
imminent. The threats from feral pigs
and nonnative plants are of high
magnitude because of their severity and
they are occurring throughout its
limited range. The threats are on-going
and therefore are imminent. We retained
a listing priority number of 2 for this
species.
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 species is known from two
populations of only five individuals in
Koaie Canyon. Myrsine mezii is
threatened by feral pigs that degrade
and destroy habitat, reduced
reproductive vigor, and stochastic
extinction due to naturally occurring
events. No known conservation
measures have been taken to date for
these threats. The threats are of a high
magnitude and imminent because of
their severity, they are occurring
throughout the limited range of M.
mezii, and are ongoing. Thus, we
retained a listing priority number of 2
for this species.
Myrsine vaccinioides (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 vaccinioides 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. Myrsine vaccinioides is
threatened by feral pigs that degrade
and destroy habitat, and nonnative
plants that compete for light and
nutrients. Pig exclusion fences protect
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some individuals of this species, and
nonnative plants have been reduced
around some individuals that are
fenced. However, these on-going
conservation efforts benefit only a small
number of the known individuals.
Further, nonnative plants will probably
never be completely eradicated because
new propagules are constantly being
dispersed into the fenced areas from
surrounding, unmanaged lands. The
species as a whole is impacted by
threats of high magnitude that are
ongoing, and thus imminent. Therefore,
we retained a listing priority number of
2 for this species.
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
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.
In some instances, illegal wetland filling
is occurring. For example, a cranberry
producer recently expanded its
operation 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 that support 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
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known threats at these sites from
recreational use and erosion, thus the
severity of these threats has been
reduced on State-owned land.
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 retained
a listing priority number of 8 for this
species.
Nothocestrum latifolium (Aiea)—The
following summary is based on
information contained in our files. No
new information was provided in the
petition received on May 11, 2004. Aiea
is a small tree found in dry to mesic
forest and diverse mesic forests on
Kauai, Oahu, Maui, Molokai, and Lanai,
Hawaii. Nothocestrum latifolium is
known from approximately a dozen
populations totaling less than 300
individuals. This species is threatened
by feral pigs, goats and cattle that may
eat it and degrade and destroy habitat,
nonnative plants that compete for light
and nutrients, and the loss of pollinators
that negatively affect the reproductive
viability of the species. Ungulates have
been fenced out of some areas where N.
latifolium currently occurs, and
nonnative plants have been reduced in
some populations that are fenced.
However, these on-going conservation
efforts for this species benefit only a few
of the known populations. The threats
are not controlled and are ongoing in
the remaining unfenced populations. In
addition, little regeneration is observed
in this species. Therefore, the threats are
of a high magnitude and imminent and
we retained a listing priority number of
2 for this species.
Ochrosia haleakalae (Holei)—The
following summary is based on
information contained in our files. No
new information was provided in the
petition 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 500 individuals on east Maui
and the island of Hawaii. Ochrosia
haleakalae is threatened by feral pigs
and goats that may directly prey upon
it and degrade and destroy habitat,
nonnative plants that compete for light
and nutrients, and fire. Feral pigs and
goats have been fenced out of the Maui
population of O. haleakalae, and fences
protect the reintroduction site in Hawaii
Volcanoes National Park on the island
of Hawaii. Nonnative plants have been
reduced in the fenced area on Maui. No
known conservation measures have
been taken to date for the other
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populations on the island of Hawaii.
The threat from fire is of a high
magnitude and imminent because no
control measures have been undertaken
to address this threat to all of the
populations. The threats from feral pigs
and goats are of a high magnitude and
ongoing to the unfenced populations of
O. haleakalae. The threat from
nonnative plants is ongoing and
imminent, and of a high magnitude to
the wild populations on the island of
Hawaii. Therefore, we retained a listing
priority number of 2 for this species.
Pediocactus peeblesianus var.
fickeiseniae (Fickeisen plains cactus)—
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 debilis (Parachute
beardtongue)—The following summary
is based on information contained in
our files. No new information was
provided in the petition received on
May 11, 2004. Parachute beardtongue is
an extremely rare plant endemic to oil
shale outcrops on the Roan Plateau
escarpment in Garfield County,
Colorado. The estimated number of
plants is 1130 to 1730. Approximately
53 to 69 percent of the plants are on
private land owned by an oil and gas
company. Most of the remaining 31 to
47 percent occur in one population on
Bureau of Land Management land that
will soon be open to leasing under a
new Resource Management Plan.
Pressure to develop energy reserves in
this area is intense. Threats include
habitat destruction caused by heavy
equipment as it traverses access roads
through plant populations. These
threats are high magnitude because of
the high number of populations affected
by these threats and the severity of the
impact. Therefore, we retained a listing
priority number of 2 for this species
based on the high magnitude of the
threats and the increase in the intensity
of energy exploration and development
in the last three years along the Roan
Plateau escarpment.
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 14 occurrences
known in Utah and one in Colorado.
Most of the occupied habitat of the
White River beardtongue is within
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developed and expanding oil and gas
fields. The location of the species’
habitat exposes it to destruction from
road, pipeline, and well-site
construction in connection with oil and
gas development. Recreational off-road
vehicle use, heavy grazing by livestock
and wildlife and livestock trampling are
additional threats. Current information
indicates that threats are nonimminent
since that are not ongoing at this time
but of a high magnitude because of their
potential to affect the majority of the
populations. Therefore, we retained a
listing priority number of 6 for this
plant variety.
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, 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. Peperomia subpetiolata is
threatened by feral pigs that may eat this
plant and degrade and destroy habitat,
and by nonnative plants that compete
for light and nutrients. All of the threats
occur range-wide and no efforts for their
control or eradication are being
undertaken. We retained a listing
priority number of 2 because the threats
are of a high magnitude and are ongoing
so are imminent.
Phacelia submutica (DeBeque
phacelia)—The following summary is
based on information contained in our
files. No new information was provided
in the petition received on May 11,
2004. DeBeque phacelia is an annual
flowering plant endemic to clay soils
derived from the Atwell Gulch and
Shire members of the Wasatch
Formation in Mesa and Garfield
Counties, Colorado. There are
approximately 40 populations, all less
than five acres. The number of plants
varies 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 are gas field development and
associated construction and
transportation activities, as well as
increased access for all-terrain vehicles.
Substantial surface disturbance alters
the unique soil structure that supports
this plant, and also destroys seed banks
that are critical to the survival of this
species. The threats are of a high
magnitude because they have the
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potential to affect the majority of the
populations and because the
populations cover such small areas of
land. The threats are nonimminent since
they are not expected to affect this
species in the next few years. Based on
nonimminent threats of a high
magnitude, we retained a listing priority
number of 8 for this species.
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 perennial herb. Currently this
species is known from three populations
totaling no more than 100 individuals in
wet forest habitat of east Maui.
Phyllostegia bracteata is threatened by
feral pigs that may directly prey upon it
and degrade and destroy habitat, and
nonnative plants that compete for light
and nutrients. The threats to P.
bracteata from pigs and nonnative
plants are of a high magnitude and
imminent because of their severity, they
are occurring range-wide, are ongoing,
and no efforts for their control have
been undertaken. Therefore, we retained
a listing priority number of 2 for this
species.
Phyllostegia floribunda (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. This species is an erect subshrub
found in mesic to wet forest on the
island of Hawaii, Hawaii. This species
is known from 13 locations totaling
fewer than 100 individuals on State,
private, and Federal lands (Hawaii
Volcanoes National Park). Only one
individual is reported at each of
approximately half of the locations.
Phyllostegia floribunda is threatened by
feral pigs that degrade and destroy
habitat, and nonnative plants that
compete for light and nutrients. Fences
protect approximately five populations
on private and Park Service lands.
Nonnative plants have been reduced in
these fenced areas. However, no
conservation efforts have been
implemented for the unfenced
populations. For the species as a whole,
the threats are ongoing and imminent,
and of a high magnitude. Consequently,
we retained a listing priority number of
2 for this species.
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. This species is a loosely spreading
many-branched vine found in wet forest
on Molokai, Hawaii. The historic range
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of this species was eastern Molokai.
Currently, P. hispida is known from
only one plant in the State of Hawaii’s
Puu Alii Natural Area Reserve. This
species is threatened by the lack of
regeneration, feral pigs that eat this
plant and degrade and/or destroy
habitat, erosion, reduced reproductive
vigor and stochastic extinction due to
naturally occurring events. No efforts for
the control of feral pigs have been
undertaken in the habitat occupied by
this species. Phyllostegia hispida is
represented in an ex-situ collection
(micropropagation) and it is unknown
whether the material will transfer to the
nursery for normal propagation methods
needed for reintroduction. The threats
are of a high magnitude and imminent
because of their severity, and they are
currently occurring throughout the
limited range of P. hispida. Thus, we
retained a listing priority number of 2
for this species.
Physaria tuplashensis, (White Bluffs
bladder-pod)—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.
Pittosporum napaliense (Hoawa)—
The following summary is based on
information contained in our files. No
new information was provided in the
petition received on May 11, 2004.
Hoawa species is a small tree found in
Pandanus forest and mesic valleys on
Kauai, Hawaii. This species is known
from about six populations totaling
several hundred individuals on the
eastern portion of the Na Pali coast.
Pittosporum napaliense is threatened by
feral pigs that degrade and destroy
habitat, and nonnative plants that
compete for light and nutrients. The
threats to P. napaliense from pigs and
nonnative plants are of a high
magnitude and imminent because of
their severity, they currently occur
range-wide, and no efforts for their
control have been undertaken.
Therefore, we retained a listing priority
number of 2 for this species.
Platanthera integrilabia (Correll) Leur
(White fringeless orchid) ‘‘ The
following summary is based on
information contained in our files. No
new information was provided in the
petition received on May 11, 2004.
Platanthera integrilabia is a perennial
herb that grows in partially, but not
fully, shaded, wet, boggy areas at the
head of streams and on seepage slopes
in Alabama, Georgia, Kentucky and
Tennessee. Historically, there were at
least 90 populations of P. integrilabia.
Currently there are only 53 extant
sites supporting the species. Several
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populations have been lost to road,
residential and commercial
construction, and to projects that altered
soil and site hydrology, and reduced site
suitability for the species. Several of the
known populations are in or adjacent to
powerline rights-of-way. Mechanical
clearing of these areas may benefit the
species by maintaining adequate light
levels; however, the use of herbicides
could pose a significant threat to the
species. All-terrain vehicles have
damaged several sites and pose a threat
to most sites. Most of the known sites
for the species occur in areas that are
managed specifically for timber
production. Timber management is not
necessarily incompatible with the
protection and management of the
species. However, care must be taken
during timber management to ensure
that the hydrology of the bogs that
support the species is not altered.
Natural succession can result in
decreased light levels. Because of the
species dependence upon moderate to
high light levels, some type of active
management to prevent complete
canopy closure is required at most
locations. Collecting for commercial and
other purposes is a threat. Herbivory
(primarily deer) threatens the species at
several sites. Protection and recovery of
this species is dependent upon active
management rather than just
preservation of its habitat. Invasive,
nonnative plants such as Japanese
honeysuckle and kudzu threaten several
sites. Given the current threats to this
species, the magnitude of threat is high.
Based upon the number of populations
and the anticipation that most of these
threats will not be realized in the next
several years, the threats are
nonimminent and, therefore, we have
assigned a listing priority number of 5
to this species.
Platydesma cornuta var. cornuta (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. This
variety 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. The
threats to P. cornuta var. cornuta
include feral pigs that directly prey
upon it and degrade and destroy habitat,
and nonnative plants that compete for
light and nutrients. All of the threats
occur range-wide and no efforts for their
control or eradication are being
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undertaken. We retained a listing
priority number of 3 for this variety
because of the high magnitude of threats
and because they are ongoing, so are
imminent.
Platydesma cornuta var. decurrens
(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. This
variety is an erect palmoid shrub found
in mesic forest on Oahu, Hawaii. This
variety is known from a few populations
totaling a few hundred individuals in
the Waianae Mountains. Platydesma
cornuta var. decurrens is threatened by
feral pigs and goats that directly prey
upon it and degrade and destroy habitat,
and nonnative plants that compete for
light and nutrients. All of the threats
occur range-wide and no efforts for their
control or eradication are being
undertaken. We retained a listing
priority number of 3 for this variety
because the threats are high in
magnitude and are ongoing, so are
imminent.
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,
2004. Platydesma remyi is a shrub or
shrubby tree found scattered in wet, low
stature 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. Platydesma remyi
is threatened by feral pigs and cattle that
degrade and destroy habitat, nonnative
plants that compete for light and
nutrients, reduced reproductive vigor,
and stochastic extinction due to
naturally occurring events. There are no
conservation efforts being implemented
to alleviate the threats to P. remyi. These
threats are ongoing and therefore,
imminent, and of a high magnitude
because of their severity and because
they are occurring throughout its
limited range. Therefore, we retained a
listing priority number of 2 for this
species.
Platydesma rostrata (Pilo kea lau
lii)—The following summary is based
on information contained in our files.
No new information was provided in
the petition received on May 11, 2004.
Pilo kea lau lii is an erect palmoid shrub
found in diverse mesic forest and
valleys on Kauai, Hawaii. This species
is known from about 20 populations
totaling several hundred individuals in
Kokee and Kuia. Platydesma rostrata is
threatened by feral goats that degrade
and destroy habitat, and nonnative
plants that compete for light and
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nutrients. Feral goats have been fenced
out of 1 of the 20 populations of P.
rostrata, and nonnative plants have
been reduced in the population that is
fenced. However, these on-going
conservation efforts benefit only 1 of the
20 known populations and, therefore,
continue to be of a high magnitude to
this species. In addition, threats to P.
rostrata are imminent because they are
ongoing in 19 of the 20 populations.
Therefore, we retained a listing priority
number of 2 for this species.
Pleomele forbesii (Hala pepe)—The
following summary is based on
information contained in our files. No
new information was provided in the
petition received on May 11, 2004.
Pleomele forbesii is a tree found in
diverse mesic and dry forests on Oahu,
Hawaii. This species is currently known
from 16 populations totaling 500
individuals. Pleomele forbesii is
threatened by predation by rats, habitat
degradation and destruction by feral
pigs and goats, fire, and nonnative
plants that compete for light and
nutrients. There are no conservation
efforts being implemented to alleviate
these threats to P. forbesii. The threats
are of a high magnitude because of their
severity and they are occurring
throughout the range of this plant in all
16 populations. The threats are ongoing
and therefore, imminent. Thus, we
retained a listing priority number of 2
for this species.
Potentilla basaltica (Soldier Meadow
cinquefoil or basalt cinquefoil)—See
above in ‘‘Summary of Listing Priority
Changes in Candidates.’’ No new
information was provided in the
petition received on May 11, 2004.
Pritchardia hardyi (Loulu)—The
following summary is based on
information contained in our files. No
new information was provided in the
petition received on May 11, 2004.
Pritchardia hardyi 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. Pritchardia hardyi is
threatened by feral pigs that degrade
and destroy habitat, and nonnative
plants that compete for light and
nutrients. Other potential threats
include direct predation of fruit by rats,
and human collection and vandalism.
No conservation efforts have been
initiated to date to alleviate these threats
to P. hardyi. The threats are of a high
magnitude because of their severity and
they are occurring throughout the range
of this plant in all three populations.
The threats are ongoing and therefore,
imminent. Thus, we retained a listing
priority number of 2 for this species.
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Pseudognaphalium (Gnaphalium)
sandwicensium var. molokaiense
(Enaena)—The following summary is
based on information contained in our
files. No new information was provided
in the petition received on May 11,
2004. Pseudognaphalium
sandwicensium var. molokaiense is a
perennial herb found in strand
vegetation in dry consolidated dunes on
Molokai, Hawaii. This variety is known
from two populations totaling a few
hundred individuals in the Moomomi
area and 25 individuals at Puu
Kahulianapa on west Maui.
Pseudognaphalium sandwicensium var.
molokaiense is threatened by axis deer
(Maui and Molokai) and feral cattle
(Molokai) that degrade and destroy
habitat, and nonnative plants that
compete for light and nutrients.
Potential threats include collection for
lei and off-road vehicles that directly
damage plants and degrade habitat.
While ungulate exclusion fences protect
one population of P. sandwicensium
var. molokaiense on Molokai and
nonnative plant control has been
implemented in this population, no
conservation efforts have been initiated
to date for the other individuals on
Molokai and Maui. The threats from
axis deer, goats, nonnative plants,
collection, and off-road vehicles are of
a high magnitude, ongoing and
imminent, because no control measures
have been undertaken for four of the
five Molokai populations or for the two
Maui populations. Therefore, we
retained a listing priority number of 3
for this variety.
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. Recent surveys
determined that the species is now
limited to four populations with a total
of 18 individuals. Psychotria grandiflora
is threatened by feral pigs and goats that
directly prey upon it and degrade and
destroy habitat, nonnative plants that
compete for light and nutrients, reduced
reproductive vigor, and stochastic
extinction due to naturally occurring
events. The threats to P. grandiflora are
of a high magnitude because of their
severity, they are occurring throughout
the plant’s limited range in all four
populations, and there are no
conservation efforts being implemented
to alleviate the threats. The threats are
also ongoing and therefore, imminent.
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Therefore, we retained a listing priority
number of 2 for this species.
Psychotria hexandra ssp. oahuensis
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 ssp. oahuensis var.
oahuensis is a tree or shrub found in
mesic and wet forests on Oahu, Hawaii.
This variety is known from three
populations of less than 20 individuals.
The other varieties of this subspecies,
hosakana and rockii, are extinct.
Psychotria hexandra ssp. oahuensis var.
oahuensis is threatened by feral pigs
and rats that consume this plant and
degrade and destroy habitat, rats that
consume its fruit, and nonnative plants
that compete for light and nutrients. All
of the threats occur range-wide, and no
efforts for their control or eradication
are being undertaken. We retained a
listing priority number of 3 because the
threats are of a high magnitude and are
ongoing, so are imminent.
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. Psychotria hobdyi is
threatened by feral goats that degrade
and destroy habitat, nonnative plants
that compete for light and nutrients, and
reduced reproductive vigor and
stochastic extinction due to naturally
occurring events. There are no
conservation measures being taken to
alleviate these threats to this species.
The threats to P. hobdyi from goats and
nonnative plants are of a high
magnitude because of their severity and
they are occurring range-wide. The
threats are imminent because they are
ongoing. Therefore, we retained a listing
priority number of 2 for this species.
Pteralyxia macrocarpa (Kaulu)—The
following summary is based on
information contained in our files. No
new information was provided in the
petition received on May 11, 2004.
Kaulu is a tree found in valleys and
slopes in diverse mesic forest on Oahu,
Hawaii. This species is known from 20
populations totaling less than 500
individuals. Pteralyxia macrocarpa is
threatened by feral pigs, rats, and the
two-spotted leafhopper that consume
this plant; by feral pigs that degrade and
destroy habitat; and, nonnative plants
that compete for light and nutrients.
These threats are of a high magnitude
because of their severity, they are
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occurring throughout its limited range,
and no efforts for their control or
eradication have been implemented.
The threats are also imminent because
they are ongoing. We retained a listing
priority number of 2 for this species.
Ranunculus hawaiensis (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 hawaiiensis is an erect or
ascending perennial herb found in
mesic to wet forest dominated by
Metrosideros polymorpha and Acacia
koa with scree substrate on Maui and
the island of Hawaii, Hawaii.
Populations formerly within Haleakala
National Park have been extirpated.
This species is known from less than
300 individuals in five populations.
However, the majority of these
individuals are seedlings, less than 1
inch (2.5 centimeters) tall, and the rate
of survival is expected to be very low.
Ranunculus hawaiiensis is threatened
by direct predation by slugs, by feral
pigs, goats, cattle, and sheep that
consume this plant and degrade and
destroy habitat, and by nonnative plants
that compete for light and nutrients.
Feral ungulates have been fenced out of
some of the populations of R.
hawaiiensis, and nonnative plants have
been reduced in some of the fenced
areas. However, feral ungulates and
nonnative plants are not controlled in
the remaining, unfenced populations. In
addition, the threat from slugs is of a
high magnitude because slugs occur
throughout the limited range of this
species and no effective measures have
been undertaken for their control.
Therefore, the threats from pigs, goats,
cattle, sheep, slugs, and nonnative
plants are of a high magnitude and
ongoing and imminent for R.
hawaiiensis. We retained a listing
priority number of 2 for this species.
Ranunculus mauiensis (Makou)—The
following summary is based on
information contained in our files. No
new information was provided in the
petition 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. This species is currently known
from less than 30 individuals on Maui
and 30 individuals on Kauai.
Ranunculus mauiensis is threatened by
feral pigs and slugs that consume it, by
habitat degradation and destruction by
feral pigs, and by nonnative plants that
compete for light and nutrients. Feral
pigs have been fenced out of the Maui
populations of R. mauiensis, and
nonnative plants have been reduced in
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the fenced areas. However, these ongoing conservation efforts benefit only
the Maui individuals and, therefore, the
threats continue to be of a high
magnitude to this species on Kauai.
Threats to the species overall are also of
a high magnitude since half of the
individuals are found on Kauai and this
represents a significant portion of the
range of R. mauiensis. In addition,
threats to R. mauiensis are imminent
because they are ongoing in the Kauai
populations. Therefore, we retained a
listing priority number of 2 for this
species.
Rorippa subumbellata (Tahoe yellow
cress)—The following summary is based
on information contained in our files
and the petition received on December
27, 2000. Tahoe yellow cress is a small
perennial herb known only from the
shores of Lake Tahoe in California and
Nevada. Data collected over the last 25
years suggest a relationship between
lake level and site occupancy by Tahoe
yellow cress. The data generally
indicate that species occurrence
fluctuates yearly as a function of both
lake level and the amount of exposed
habitat. Records kept since 1900
indicate preponderance of years with
high lake levels that would isolate and
reduce Tahoe yellow cress occurrences
at higher beach elevations. From the
standpoint of the species, less favorable
peak years have occurred almost twice
as often as more favorable low-level
years. In addition, there has been
widespread and intensive use of the
shorezone since European settlement.
Today, shorezone conditions are
influenced by heavy recreational use,
boating, construction of piers and boat
launches, and dam operations that
control lake elevation. Annual surveys
are conducted to determine population
numbers, site occupancy, and general
disturbance regime. During the 2003
and 2004 annual survey period, the lake
level was approximately 6,224 feet
(1,898 meters). 2003 was the third
consecutive year of low water. The
survey located Tahoe yellow cress at 45
of the 72 sites surveyed (65 percent
occupied), up from 15 sites (19 percent
occupied) in 2000 when the lake level
was high at 6,228 feet. Approximately
25,200 stems were counted or estimated
in 2003, whereas during the 2000
annual survey, the estimated number of
stems was 4,590. A methodology change
in 2004 resulted in fewer numbers; the
new methodology proved unworkable
and was abandoned in 2005. Lake levels
were higher in 2005, and less habitat
was available; a summary of survey
results is not yet available, but total
numbers of sites and individuals are
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expected to be lower than in the period
2001–2003.
Many Tahoe yellow cress sites are
intensively used for commercial and
public purposes, and are subject to
various activities such as erosion
control, marina developments, pier
construction, and recreation. The U.S.
Forest Service, California Tahoe
Conservancy, and California Department
of Parks and Recreation protect Tahoe
yellow cress with management
programs that include monitoring,
fenced enclosures, and transplanting
efforts when funds and staff are
available. Public agencies (including the
Service), private landowners, and
environmental groups collaborated to
develop a conservation strategy coupled
with a Memorandum of Understanding/
Conservation Agreement. The
conservation strategy, which was
completed in 2003 and contains goals
and objectives for recovery and survival,
a research and monitoring agenda, and
will serve as the foundation for an
adaptive management program. Because
of the continued commitments to
conservation demonstrated by
regulatory and land management
agencies participating in the
conservation strategy, we have
determined the threats to Tahoe yellow
cress from various land uses have been
reduced to a moderate magnitude. In
high lake level years such as 2005,
however, recreational use is
concentrated within Tahoe yellow cress
habitat, and we consider this threat in
particular to be ongoing and imminent.
Therefore, we are maintaining an LPN of
8 for this species.
Schiedea 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 species is known
from one population of less than 20
individuals on the cliffs of Kalalau
Valley. Schiedea attenuata is threatened
by feral goats that directly prey upon it
and degrade and destroy habitat, and
nonnative plants that compete for light
and nutrients. These threats are of a
high magnitude because they are
occurring throughout its limited range.
Threats continue to be imminent
because they are ongoing and because of
the potential for the elimination of the
only known population by a single
stochastic or naturally occurring event.
Therefore, we retained a listing priority
number of 2 for this species.
Schiedea pubescens (Maolioli)—The
following summary is based on
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information contained in our files. No
new information was provided in the
petition received on May 11, 2004.
Schiedea pubescens is a reclining or
weakly climbing vine found in diverse
mesic to wet forest on Maui and
Molokai, Hawaii. Currently, this species
is known from six populations totaling
approximately 100 individuals on Maui
and Molokai. Schiedea pubescens is
threatened by feral goats that consume
it and degrade and destroy habitat, and
by nonnative plants that compete for
light and nutrients. Feral ungulates have
been fenced out of the population of S.
pubescens on Hawaii and feral goats
have been fenced out of a few of the
west Maui populations of S. pubescens.
Nonnative plants have been reduced in
the populations that are fenced on Maui.
However, the threats are not controlled
and are ongoing in the remaining
unfenced populations on Maui and the
three populations on Molokai. In light of
the extremely low number of
individuals of this species, the threats
from goats and nonnative plants are of
a high magnitude and imminent for S.
pubescens and we retained 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. Currently, this species is
declining throughout its range, and is
known from several populations totaling
100 to 300 individuals, typically of 25
individuals per population. This species
is threatened by cattle that may directly
prey upon it and degrade and destroy
habitat, fire, and nonnative plants that
compete for light and nutrients. This
species is represented in an ex-situ
collection. All of the threats occur
range-wide, and no efforts for their
control or eradication are being
undertaken. We retained a listing
priority number of 2 because the threats
are of a high magnitude because of their
severity and are ongoing, so are
imminent.
Sedum eastwoodiae (Red Mountain
stonecrop)—The following summary is
based on information contained in our
files and information provided by the
California Department of Fish and
Game. 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, between 1,900 and 4,000 feet
elevation. Its distribution is limited to
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Red Mountain, Mendocino County,
California, where it occupies 30 acres
scattered over 4 square miles. Total
population size is estimated at between
5,300 and 23,000 plants, contained
within 27 habitat polygons. Intensive
monitoring suggests considerable
annual variation in plant seedling
success and inflorescence production;
stonecrop density varied from year-toyear.
The primary threat to the species is
the potential for surface mining for
chromium and nickel. The entire
distribution Red Mountain stonecrop is
either owned by mining interests, or is
covered by mining claims, none of
which are currently active. Surface
mining would destroy habitat suitability
for this species. The species is also
believed to be threatened by tree and
shrub encroachment into its habitat, in
absence of fire. Given the magnitude
(high) and immediacy (nonimminent) of
the threat to the small, scattered
populations, and its taxonomy (species),
we assigned a listing priority number of
5 to this species.
Sicyos macrophyllus (Anunu)—The
following summary is based on
information contained in our files. No
new information was provided in the
petition received on May 11, 2004.
Sicyos macrophyllus is a perennial vine
found in wet Metrosideros polymorpha
(ohia) forest and subalpine Sophora
chrysophylla-Myoporum sandwicense
(mamane-naio) 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 and in
Hawaii Volcanoes National Park (Puna
area) on the island of Hawaii. It appears
that a naturally occurring population at
Kipuka Ki in Hawaii Volcanoes National
Park is reproducing on its own by seeds,
but seeds have not been successfully
germinated under nursery conditions.
This species is threatened by feral pigs
and sheep that degrade and destroy
habitat, and nonnative plants that
compete for light and nutrients. Feral
pigs have been fenced out of some of the
areas where S. macrophyllus currently
occurs, but the fences do not exclude
sheep. Nonnative plants have been
reduced in the populations that are
fenced. However, the threats are not
controlled and are ongoing in the
remaining, unfenced populations, and
are, therefore, of a high magnitude and
are imminent. In addition, the threat
from sheep is of a high magnitude, and
ongoing and imminent, in all
populations because the current fences
do not exclude sheep. Therefore, we
retained a listing priority number of 2
for this species.
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Solanum nelsonii (Popolo)—The
following summary is based on
information contained in our files. No
new information was provided in the
petition received on May 11, 2004.
Solanum nelsonii is a sprawling or
trailing shrub found in coral rubble or
sand in coastal sites on the islands of
Hawaii, Molokai, Maui, Niihau, Nihoa,
and Pearl and Hermes, Hawaii. This
species is known from ten populations
totaling fewer than 300 individuals, and
is declining rapidly on all islands. On
Maui and the island of Hawaii, S.
nelsonii is threatened by development,
off-road vehicles, and trampling that
degrades and/or destroys habitat, and
nonnative plants that compete for light
and nutrients. On Molokai, the major
threats to S. nelsonii are wild cattle and
axis deer that adversely modify habitat,
and nonnative plants. On Nihoa, and
Pearl and Hermes Atoll this species is
threatened by nonnative plants. Threats
to this species on Niihau are unknown.
There are no conservation measures
being taken to alleviate the threats to S.
nelsonii on Maui and the island of
Hawaii. On Molokai, conservation
measures for this species include
ungulate exclusion fences and weed
control. On the island of Nihoa, and
Pearl and Hermes Atoll, there is no
public or recreational use allowed as
these islands are within the Hawaiian
Islands National Wildlife Refuge
(Refuge). Limited nonnative plant
control is conducted in the refuge.
Solanum nelsonii is represented in exsitu collections and in seed storage.
Currently, conservation measures have
been implemented to the benefit of the
individuals on Molokai and within the
Refuge. However, there are no efforts to
control the ongoing threats to this
species on the islands of Hawaii and
Maui. Therefore, the threats continue to
be of a high magnitude to S. nelsonii,
and we retained a listing priority
number of 2 for this species because the
threats are of a high magnitude and are
imminent.
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
on the island of Hawaii, Hawaii.
Stenogyne cranwelliae is known from
six populations with a total of 100
individuals. This species is threatened
by feral pigs that degrade and destroy
habitat, and nonnative plants that
compete for light and nutrients. In
addition, this species is potentially
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threatened by rats that may directly prey
upon it. All of the threats occur rangewide and no efforts for their control or
eradication are being undertaken. We
retained a listing priority number of 2
because the threats are of a high
magnitude and are ongoing, so are
imminent.
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 five populations totaling
100 to 200 individuals in the
northwestern section of the island of
Kauai. Stenogyne kealiae is threatened
by feral pigs and goats, and deer that
degrade and destroy habitat and may
directly prey upon it, and by nonnative
plants that compete for light and
nutrients. The threats to S. kealiae from
pigs, goats, deer, and nonnative plants
are of a high magnitude because of their
severity, they are occurring range-wide,
and no efforts for their control have
been undertaken. The threats are also
imminent because they are ongoing.
Therefore, we retained 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.
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 one of the five states in which it
originally occurred. 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.
Georgia aster has apparently been
eliminated from 4 counties in Alabama,
1 county in Florida, 11 counties in
Georgia, 1 county in North Carolina, and
5 counties in South Carolina; it remains
in 31 counties in 4 states (NC, SC, AL,
& GA). Most remaining populations of
this species survive adjacent to roads,
railroads, utility rights-of-way and other
openings where land management
occasionally mimics natural disturbance
regimes, but where they are vulnerable
to accidental destruction from herbicide
application, road shoulder grading, and
other maintenance activities. Many
populations are now threatened also by
development (several are within
planned residential subdivisions),
highway expansion/improvement, and
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by woody succession due to fire
suppression. The severity of threats
faced by this species is high and the
threats are operating throughout its
range. We are not aware of ongoing
efforts to abate these threats or
otherwise protect existing populations.
Therefore, the magnitude of threats is
assessed to be high, but because the
species appears to tolerate some level of
disturbance, we regard the threats as
nonimminent and thus, we retained a
listing priority 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.
Zanthoxylum oahuense is small tree
found in mesic to wet forest habitat on
Oahu, Hawaii. Currently this species is
known from several populations totaling
approximately 500 individuals on Oahu.
Zanthoxylum oahuense is threatened by
feral pigs that directly prey upon it and
degrade and destroy habitat, nonnative
plants that compete for light and
nutrients, and the black twig borer. All
of the threats occur range-wide and no
efforts for their control or eradication
are being undertaken. We retained a
listing priority number of 2 for this
species because the threats are
rangewide and, therefore, of a high
magnitude and are ongoing, so are
imminent.
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). Fourteen populations are
currently known to exist: One in Alaska
(Wrangell County), two in Colorado (El
Paso County), four in Montana (Glacier
County), three in Oregon (Wallowa
County), one in Washington (Ferry
County), one in Wyoming (Crook
County), one in Alberta, Canada, and
one in the Yukon Territory, Canada.
Collectively, these 14 sites occur over a
large area of western North America.
Three additional populations, two in
Nevada and one in Idaho, were
discovered in surveys conducted in
2001; however, genetic analysis
indicated that the plants contain B.
lineare alleles but they are not pure B.
lineare individuals. No extant
populations are known east of the Rocky
Mountains. Most sites occupied by B.
lineare are generally small, with most
less than 465 square meters (5,000
square feet) in area. Botrychium lineare
populations range in size from 2 to 162
plants, with 6 populations supporting
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more than 15 individuals. The total
number of individuals observed at the
14 extant population sites varies, with
observations ranging from 2 to 100
individuals. Eleven of the 12 B. lineare
populations in the U.S. occur on Federal
or Tribal land.
Most B. lineare sites are impacted by
disturbances including grazing by native
and nonnative animals, trampling from
hikers, avalanches, and impacts from
vehicles. The effects of these various
disturbances and their relative level of
impact in maintaining or eliminating
habitat have not been investigated for
the species. Six of the Botrychium
lineare sites, one in Alaska, four in
Montana, and one in Wyoming, are
located adjacent to disturbed roadsides
or all-terrain vehicle trails and may be
affected by roadside traffic or by road
maintenance activities, such as
herbicide spraying or mowing. The
largest known site of B. lineare located
along a roadside was sprayed in 2000,
although impacts on the population are
unknown. Toadflax, an aggressive,
difficult-to-control, nonnative plant,
was introduced from the Pikes Peak
roadway into two B. lineare sites in
Colorado. Other nonnative plants are
associated with B. lineare sites
throughout the species’ range and
should be regarded as potential threats
to the species. Grazing by livestock or
wildlife is a potential threat if it occurs
prior to the maturation and release of
spores thus compromising the capacity
for sexual reproduction of affected
plants. Regulatory mechanisms may be
inadequate to protect this species in
Forest Service Regions 1 and 4, which
include sites found in Montana, Nevada,
Utah, and Idaho, because in those
Regions B. lineare is not included on
their regional sensitive species lists.
Botrychium lineare is not on Canada’s
list of threatened or vulnerable species,
so there is no special protection for this
species in Canada.
The generally small size of most
existing B. lineare populations (less
than 465 square meters (5,000 square
feet)) makes this species not only
difficult to locate, but also vulnerable to
extirpation due to random naturally
occurring events. A single random
environmental event could extirpate a
portion or all of the individuals at a
given site. Conversely, the disjunct
nature of existing population sites over
a wide geographic range covering at
least six western states and two
Canadian provinces indicates a high
likelihood that additional, undetected B.
lineare population sites exist. This is
especially true of the more northern
latitudes where the species was until
last year, not previously located.
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Because the plant is distributed over
a wide range and because the species is
more difficult to locate than most other
plant species, we expect that more
populations will continue to be
discovered in the future. Because the
species is adapted to some level of
disturbance and seems to persist in
disturbed environments, the threats are
not high in magnitude. In addition,
since most populations (10 of 14) occur
on Federal lands and are afforded some
level of protection, threats are currently
nonimminent. For these reasons, we
assigned a listing priority number of 11
to this species.
Christella boydiae (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. 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 island. Currently,
this species is known from three
populations with a combined total of
362 to 422 individuals. The three
populations are found in Kipahulu
Valley and Waihoi Valley on Maui, and
the Koolau Mountains of Oahu. Current
populations survive only at the extreme
upper elevations of streambanks.
This species is threatened by feral
pigs and goats that degrade and/or
destroy habitat and that may eat this
plant, nonnative plants that compete for
light and nutrients, man-made stream
diversion, and erosion. Feral pigs and
goats have been fenced out of one of the
three populations of C. boydiae and
nonnative plants have been reduced in
the fenced area. Although one of the
three populations of this species has
been fenced and weeds are being
controlled in the fenced area, no
conservation efforts are underway to
alleviate these threats to the other two
populations. In addition, no
conservation measures have been taken
to address the threats from stream
diversions and erosion throughout the
range of C. boydiae. The threats to C.
boydiae are imminent and of a high
magnitude because they are ongoing in
two of only three known populations.
Therefore, we retained a listing priority
number of 2 for this species.
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
fern found in dry shrubland and
grassland on Oahu, Hawaii. This newly
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described species is found only on the
island of Oahu on the slopes of
Diamond Head Crater in one population
totaling hundreds of individuals. This
species is threatened by fire that
degrades and/or destroys habitat, and
nonnative plants that compete for light
and nutrients. Potential threats to D.
takeuchii include human trampling and
erosion of its steep hillside habitat. The
magnitude of threats continues to be
high because no conservation measures
have been taken to address them.
Threats continue to be imminent
because they are ongoing and because of
the potential for the elimination of the
only known population by a single
stochastic or naturally occurring event.
We retained a listing priority number of
2 for this species.
Huperzia stemmermanniae (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.
Waewaeiole is found in mesic
Metrosideros polymorpha-Acacia koa
(ohia-koa) forests on the islands of Maui
and Hawaii, Hawaii. Only four
populations are known, totaling less
than 20 individuals on Hawaii and
Maui. Huperzia stemmermanniae is
threatened by feral pigs, goats, and
cattle that degrade and/or destroy
habitat, fire, and nonnative plants that
compete for light, space, and nutrients.
The threats to H. stemmermanniae from
pigs, goats, cattle, fire, and nonnative
plants are of a high magnitude and
imminent because of their severity, they
are occurring range-wide, no efforts for
their control have been undertaken, and
they are ongoing. Therefore, we retained
a listing priority number of 2 for this
species.
Microlepia strigosa var. mauiensis
(Palapalai)—The following summary is
based on information contained in our
files. No new information was provided
in the petition received on May 11,
2004. Palapalai is a fern found in mesic
to wet forests. It is currently found only
on the island of Maui, where it is known
from three populations totaling 100 to
200 individuals. Microlepia strigosa var.
mauiensis is threatened by feral pigs
that degrade and destroy habitat,
nonnative plants that compete for light
and nutrients, reduced reproductive
vigor, and stochastic extinction due to
naturally occurring events. Feral pigs
have been fenced out of at least one area
on Maui where M. strigosa var.
mauiensis currently occurs, and
nonnative plants have been reduced in
the fenced area. However, the threats are
not controlled and are ongoing in the
remaining unfenced populations on
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Maui and all three of the populations on
the island of Hawaii. Therefore, the
threats from feral pigs and nonnative
plants are of a high magnitude and
imminent and we retained a listing
priority number of 3 for M. strigosa var.
mauiensis.
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 five species
(which are listed below) is currently
warranted but precluded by work
identified above (see ‘‘Petition Findings
for Candidate Species’’ above). One of
the primary reasons that the work
identified above is higher priority is that
these species are currently listed as
threatened under the Act, and therefore
they already receive certain protections
under the Act. The Service promulgated
regulations extending take prohibitions
for endangered species under section 9
to threatened species (50 CFR 17.31).
Prohibited actions under section 9
include, but are not limited to, take (i.e.,
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
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 U.S.,
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 (sq-km)) 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
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number of 3 for uplisting to 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 U.S. 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 U.S.,
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 assigned a listing
priority number of 3 for uplisting to this
population due to continuing high
levels of human-caused mortality, new
threats to habitat in the form of largescale mine development proposals in
the Cabinet Mountains, and the high
potential for further fragmentation of
populations within the recovery zone.
(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 U.S., 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 square mile (5,700 square
kilometer) 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 humancaused mortality, and small population
size and population fragmentation that
produce genetic isolation. We assigned
a listing priority number of 3 for
uplisting to this population because of
continuing high levels of human-caused
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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 kilometers (289
miles) of stream in portions of the upper
Gila River (Grant, Catron, and Hidalgo
Counties, New Mexico); middle Gila
River (Pinal County, Arizona); lower
San Pedro River (Pinal County,
Arizona); Aravaipa Creek (Graham and
Pinal Counties, Arizona); Eagle Creek
(Graham and Greenlee Counties,
Arizona); and the Verde River (Yavaipai
County, Arizona). Its present range is
only about 10 to 15 percent of the
historic range, and the status of the
species 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
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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. Federal agencies have
reduced grazing pressures by removing
cattle from the mainstem of most rivers;
however, grazing in the uplands
continues to affect watershed condition.
Groundwater withdrawals or exchanges
that affect streamflow are not reversible.
The threats are high in magnitude
because effects from nonnative species
introductions are permanent, unless
streams are actively renovated and/or
barriers installed to preclude further
recolonization by nonnatives and
groundwater withdrawals or exchanges
that affect streamflow are not reversible.
Because these high magnitude threats
have gone on for many years in the past,
and are ongoing, the threats are
imminent. Therefore, we assigned this
species a listing priority of 1 for
uplisting to endangered. Note on
December 20, 2005, we published a
proposed critical habitat rule (70 FR
75545) for this species.
(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
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
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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.
Federal agencies have reduced grazing
pressures by removing cattle from the
mainstem of most rivers; however,
grazing in the uplands continues to
affect watershed condition.
Groundwater withdrawals or exchanges
that affect streamflow are not reversible.
Most of these high-magnitude 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 (e.g., water
exchanges), or are not easily reversed
(e.g., nonnative stocking and impacts
from grazing), the threats are high in
magnitude and imminent. Therefore, we
assigned this species a listing priority
number of 1 for uplisting to endangered.
Note on December 20, 2005, we
published a proposed critical habitat
rule (70 FR 75545) for this species.
Current Notice of Review
We gather data on plants and animals
native to the U.S. that appear to merit
consideration for addition to the Lists of
Endangered and Threatened Wildlife
and Plants. This notice identifies those
species that we currently regard as
candidates for addition to the Lists.
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
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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
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
PO 00000
Frm 00071
Fmt 4701
Sfmt 4702
53825
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).
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
species or as candidates in the previous
CNOR (published May 11, 2005) that are
no longer proposed species or
candidates for listing. Since May 11,
2005, we added 19 of these species to
the Lists of Endangered and Threatened
Wildlife and Plants and removed 14
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
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Federal Register / Vol. 71, No. 176 / Tuesday, September 12, 2006 / Proposed Rules
following codes (not all of these codes
may have been used in this CNOR):
A—Species that are more abundant or
widespread than previously believed
and species that are not subject to the
degree of threats sufficient to warrant
continuing candidate status, or issuing a
proposed or final listing.
F—Species whose range no longer
includes a U.S. territory.
I—Species for which we have
insufficient information on biological
vulnerability and threats to support
issuance of a proposed rule to list.
L—Species we added to the Lists of
Endangered and Threatened Wildlife
and Plants.
M—Species we mistakenly included
as candidates or proposed species in the
last notice of review.
N—Species that are not listable
entities based on the Act’s definition of
‘‘species’’ and current taxonomic
understanding.
U—Species not subject to the degree
of threats sufficient to warrant issuance
of a proposed listing or continuance of
candidate status due, in part or totally,
to conservation efforts that remove or
reduce the threats to the species.
X—Species we believe to be extinct.
The columns describing lead region,
scientific name, family, common name,
and historical range include information
as previously described for Table 1.
sroberts on PROD1PC70 with PROPOSALS
Request for Information
We request you submit any further
information on the species named in
this notice as soon as possible or
whenever it becomes available. We are
particularly interested in any
information:
(1) Indicating that we should add a
species to the list of candidate species;
(2) indicating that we should remove
a species from candidate status;
(3) recommending areas that we
should designate as critical habitat for a
species, or indicating that designation of
critical habitat would not be prudent for
a species;
(4) documenting threats to any of the
included species;
(5) describing the immediacy or
magnitude of threats facing candidate
species;
(6) pointing out taxonomic or
nomenclature changes for any of the
species;
VerDate Aug<31>2005
16:24 Sep 11, 2006
Jkt 208001
(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. Hawaii, Idaho, Oregon,
Washington, American Samoa, Guam,
and Commonwealth of the Northern
Mariana Islands. Regional Director
(TE), U.S. Fish and Wildlife Service,
Eastside Federal Complex, 911 NE.
11th Avenue, Portland, Oregon
97232–4181 (503/231–6158).
California/Nevada Operations Office
(CNO). California and Nevada.
Regional Director (TE), U.S. Fish and
Wildlife Service, 2800 Cottage Way,
Suite W2606, Sacramento, California
95825.
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
PO 00000
Frm 00072
Fmt 4701
Sfmt 4702
Director (TE), U.S. Fish and Wildlife
Service, P.O. Box 25486, Denver
Federal Center, Denver, Colorado
80225–0486 (303/236–7400).
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 review
during regular business hours.
Individual respondents may request that
we withhold their home addresses from
the rulemaking record, which we will
honor to the extent allowable by law.
There also may be circumstances in
which we would withhold from the
record a respondent’s identity, as
allowable by law. If you wish us to
withhold your name and/or address,
you must state this prominently at the
beginning of your comment, but you
should be aware that the Service may be
required to disclose your name and
address pursuant to the Freedom of
Information Act. 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 notice is published under
the authority of the Endangered Species Act
(16 U.S.C. 1531 et seq.).
Dated: August 23, 2006.
Marshall Jones,
Director, Fish and Wildlife Service.
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53827
TABLE 1.—CANDIDATE NOTICE OF REVIEW (ANIMALS AND PLANTS)
[Note: See end of SUPPLEMENTARY INFORMATION for an explanation of symbols used in this table.]
Status
Category
Lead
region
Priority
Scientific name
Family
Common name
Historic range
MAMMALS
C* .............
3
R1 ............
Emballonura semicaudata
rotensis.
Emballonuridae ...
C* .............
3
R1 ............
Emballonura semicaudata
semicaudata.
Emballonuridae ...
C* .............
2
R5 ............
Sylvilagus transitionalis ....
Leporidae ............
C* .............
6
CNO .........
Martes pennanti ...............
Mustelidae ...........
C* .............
3
R1 ............
Geomyidae ..........
C* .............
3
R1 ............
C* .............
3
R1 ............
Thomomys mazama
couchi.
Thomomys mazama
glacialis.
Thomomys mazama louiei
C* .............
3
R1 ............
Geomyidae ..........
C* .............
3
R1 ............
C* .............
3
R1 ............
C* .............
3
R1 ............
C* .............
3
R1 ............
C* .............
3
CNO .........
Thomomys mazama
melanops.
Thomomys mazama
pugetensis.
Thomomys mazama
tacomensis.
Thomomys mazama
tumuli.
Thomomys mazama
yelmensis.
Spermophilus tereticaudus
chlorus.
C* .............
9
R1 ............
Sciuridae .............
C* .............
5
R1 ............
Spermophilus brunneus
endemicus.
Spermophilus washingtoni
Geomyidae ..........
Geomyidae ..........
Geomyidae ..........
Geomyidae ..........
Geomyidae ..........
Geomyidae ..........
Sciuridae .............
Sciuridae .............
Bat, Pacific sheath-tailed
U.S.A. (GU, CNMI).
(Mariana Islands subspecies).
Bat, Pacific sheath-tailed
U.S.A. (AS), Fiji, Inde(American Samoa DPS).
pendent Samoa, Tonga,
Vanuatu.
Cottontail, New England .. U.S.A. (CT, MA, ME, NH,
NY, RI, VT).
Fisher (west coast DPS) .. U.S.A. (CA, CT, IA, ID, IL,
IN, KY, MA, MD, ME,
MI, MN, MT, ND, NH,
NJ, NY, OH, OR, PA,
RI, TN, UT, VA, VT,
WA, WI, WV, WY),
Canada.
Pocket gopher, Mazama
U.S.A. (WA).
(Shelton).
Pocket gopher, Mazama
U.S.A. (WA).
(Roy Prairie).
Pocket gopher, Mazama
U.S.A. (WA).
(Cathlamet).
Pocket gopher, Mazama
U.S.A. (WA).
(Olympic).
Pocket gopher, Mazama
U.S.A. (WA).
(Olympia).
Pocket gopher, Mazama
U.S.A. (WA).
(Tacoma).
Pocket gopher, Mazama
U.S.A. (WA).
(Tenino).
Pocket gopher, Mazama
U.S.A. (WA).
(Yelm).
Squirrel, Palm Springs (=
U.S.A. (CA).
Coachella Valley)
round-tailed ground.
Squirrel, Southern Idaho
U.S.A. (ID).
ground.
Squirrel, Washington
U.S.A. (WA, OR).
ground.
BIRDS
3
R1 ............
Porzana tabuensis ...........
Rallidae ...............
C* .............
C* .............
2
3
R1 ............
CNO .........
Oreomystis bairdi .............
Coccyzus americanus ......
Fringillidae ...........
Cuculidae ............
C* .............
6
R1 ............
Gallicolumba stairi ............
Columbidae .........
C* .............
3
R1 ............
6
R5 ............
Eremophila alpestris
strigata.
Calidris canutus rufa ........
Alaudidae ............
C* .............
C* .............
sroberts on PROD1PC70 with PROPOSALS
C* .............
5
R7 ............
C* .............
2
CNO .........
C* .............
8
R2 ............
C* .............
6
R1 ............
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17:59 Sep 11, 2006
Brachyramphus
brevirostris.
Synthliboramphus
hypoleucus.
Tympanuchus
pallidicinctus.
Centrocercus
urophasianus.
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Alcidae .................
U.S.A. (AS), Australia, Fiji,
Independent Samoa,
Marquesas, Philippines,
Society Islands, Tonga.
Creeper, Kauai ................. U.S.A. (HI).
Cuckoo, yellow-billed
U.S.A. (Lower 48 States),
(Western U.S. DPS).
Canada, Mexico, Central and South America.
Ground-dove, friendly
U.S.A. (AS), Independent
(American Samoa DPS).
Samoa.
Horned lark, streaked ...... U.S.A. (OR, WA), Canada
(BC).
Knot, red .......................... U.S.A. (Atlantic coast),
Canada, South America.
Murrelet, Kittlitz’s .............. U.S.A. (AK), Russia.
Alcidae .................
Murrelet, Xantus’s ............
U.S.A. (CA), Mexico.
Phasianidae .........
Prairie-chicken, lesser ......
Phasianidae .........
Sage-grouse, greater (Columbia Basin DPS).
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).
Scolopacidae .......
Fmt 4701
Sfmt 4702
Crake, spotless (American
Samoa DPS).
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TABLE 1.—CANDIDATE NOTICE OF REVIEW (ANIMALS AND PLANTS)—Continued
[Note: See end of SUPPLEMENTARY INFORMATION for an explanation of symbols used in this table.]
Status
Category
Lead
region
Priority
Scientific name
Family
Common name
C* .............
3
R1 ............
Oceanodroma castro .......
Hydrobatidae .......
Storm-petrel, bandrumped (Hawaii DPS).
C* .............
5
R4 ............
Dendroica angelae ...........
Emberizidae ........
Warbler, elfin woods ........
Historic range
U.S.A. (HI), Atlantic
Ocean, Ecuador (Galapagos Islands), Japan.
U.S.A. (PR).
REPTILES
C* .............
C* .............
2
9
R2 ............
R3 ............
Sceloporus arenicolus ......
Sistrurus catenatus
catenatus.
Iguanidae .............
Viperidae .............
Lizard, sand dune ............
Massasauga
(=rattlesnake), eastern.
C* .............
3
R4 ............
Colubridae ...........
Snake, black pine ............
C* .............
C* .............
8
3
R4 ............
R2 ............
Pituophis melanoleucus
lodingi.
Pituophis ruthveni ............
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 ...........
Kinosternidae ......
Snake, Louisiana pine .....
Turtle, Sonoyta mud ........
U.S.A. (LA, 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
CNO .........
Rana luteiventris ..............
Ranidae ...............
Frog, Columbia spotted
(Great Basin DPS).
C* .............
3
CNO .........
Rana muscosa .................
Ranidae ...............
C* .............
2
R1 ............
Rana pretiosa ...................
Ranidae ...............
Frog, mountain yellowlegged (Sierra Nevada
DPS).
Frog, Oregon spotted .......
C* .............
C* .............
11
3
CNO .........
R3 ............
Ranidae ...............
Crytobranchidae ..
Frog, relict leopard ...........
Hellbender, Ozark ............
C*
C*
C*
C*
C*
2
2
2
11
2
R2 ............
R2 ............
R2 ............
CNO .........
R4 ............
Rana onca ........................
Cryptobranchus
alleganiensis bishopi.
Eurycea waterlooensis .....
Eurycea naufragia ............
Eurycea chisholmensis ....
Bufo canorus ....................
Necturus alabamensis .....
Plethodontidae ....
Plethodontidae ....
Plethodontidae ....
Bufonidae ............
Proteidae .............
Salamander, Austin blind
Salamander, Georgetown
Salamander, Salado ........
Toad, Yosemite ................
Waterdog, black warrior
(=Sipsey Fork).
U.S.A.
U.S.A.
U.S.A.
U.S.A.
U.S.A.
U.S.A. (CA).
U.S.A. (AZ, NM).
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. (CA, OR, WA),
Canada (BC).
U.S.A. (AZ, NV, UT).
U.S.A. (AR, MO).
(TX).
(TX).
(TX).
(CA).
(AL).
FISHES
PE ............
C* .............
C* .............
C*
C*
C*
C*
C*
3
2
11
CNO .........
R2 ............
R6 ............
Gila bicolor vaccaceps .....
Gila nigra ..........................
Etheostoma cragini ..........
Cyprinidae ...........
Cyprinidae ...........
Percidae ..............
Chub, Cowhead Lake tui
Chub, headwater ..............
Darter, Arkansas ..............
.............
.............
.............
.............
.............
5
5
2
2
3
R4
R4
R4
R4
R6
............
............
............
............
............
Etheostoma susanae .......
Percina aurora .................
Etheostoma phytophilum
Etheostoma moorei ..........
Thymallus arcticus ...........
Percidae ..............
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 ......
PSAT ........
N/A
Noturus crypticus .............
Moxostoma sp. .................
Cottus sp. .........................
Notropis oxyrhynchus ......
Notropis buccula ..............
Catostomus discobolus
yarrowi.
Salvelinus malma .............
Darter, Cumberland .........
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 .....
Salmonidae .........
Trout, Dolly Varden ..........
U.S.A. (AK, WA), Canada,
East Asia.
R1 ............
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).
sroberts on PROD1PC70 with PROPOSALS
CLAMS
C* .............
C ...............
5
2
R4 ............
R3 ............
Villosa choctawensis ........
Villosa fabalis ...................
Unionidae ............
Unionidae ............
Bean, Choctaw .................
Bean, rayed ......................
C ...............
2
R4 ............
Unionidae ............
Ebonyshell, round ............
C* .............
2
R2 ............
Fusconaia (=Obovaria)
rotulata.
Popenaias popei ..............
U.S.A. (AL, FL).
U.S.A. (IL, IN, KY, MI, NY,
OH, TN, PA, VA, WV),
Canada (ON).
U.S.A. (AL, FL).
Unionidae ............
Hornshell, Texas ..............
U.S.A. (NM, TX), Mexico.
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TABLE 1.—CANDIDATE NOTICE OF REVIEW (ANIMALS AND PLANTS)—Continued
[Note: See end of SUPPLEMENTARY INFORMATION for an explanation of symbols used in this table.]
Status
Category
Lead
region
Priority
Scientific name
Family
Common name
Historic range
Ptychobranchus
subtentum.
Ptychobranchus jonesi .....
Lampsilis rafinesqueana ..
Plethobasus cyphyus .......
Unionidae ............
Kidneyshell, fluted ............
U.S.A. (AL, KY, TN, VA).
Unionidae ............
Unionidae ............
Unionidae ............
Kidneyshell, southern .......
Mucket, Neosho ...............
Mussel, sheepnose ..........
Margaritiferidae ...
Unionidae ............
Unionidae ............
Unionidae ............
Unionidae ............
Unionidae ............
Unionidae ............
Pearlshell, Alabama .........
Pearlymussel, slabside ....
Pigtoe, fuzzy ....................
Pigtoe, Georgia ................
Pigtoe, narrow ..................
Pigtoe, tapered .................
Sandshell, southern .........
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).
Margaritiferidae ...
Spectaclecase ..................
Unionidae ............
Spinymussel, Altamaha ...
U.S.A. (AL, AR, IA, IN, IL,
KS, KY, MO, MN, NE,
OH, TN, VA, WI, WV).
U.S.A. (GA).
Pleuroceridae ......
Pleuroceridae ......
Oreohelicidae ......
Hornsnail, rough ...............
Mudalia, black ..................
Mountainsnail, Ogden ......
U.S.A. (AL).
U.S.A. (AL).
U.S.A. (UT).
Lymnaeidae .........
Pleuroceridae ......
Pondsnail, Bonneville .......
Rocksnail, Interrupted
(=Georgia).
Sisi snail ...........................
Snail, Diamond Y Spring
U.S.A. (UT).
U.S.A. (GA, AL).
Snail, fragile tree ..............
Snail, Guam tree ..............
Snail, Humped tree ..........
Snail, Lanai tree ...............
Snail, Lanai tree ...............
Snail, Langford’s tree .......
Snail, Phantom cave ........
Snail, Tutuila tree .............
Springsnail, Chupadera ...
Springsnail, elongate mud
meadows.
Springsnail, Gila ...............
Springsnail, Gonzales ......
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.
Springsnail, Huachuca .....
Springsnail, New Mexico
Springsnail, Page .............
Springsnail (=Tryonia),
Phantom.
Springsnail, Three Forks ..
Tree snail, Newcomb’s ....
U.S.A.
U.S.A.
U.S.A.
U.S.A.
Beetle, Warm Springs
Zaitzevian riffle.
Bug, Wekiu .......................
Butterfly, Florida leafwing
Butterfly, Mariana eightspot.
Butterfly, Mariana wandering.
Butterfly, Miami blue ........
U.S.A. (MT).
Caddisfly, Sequatchie ......
Cave beetle, Baker Station (=insular).
U.S.A. (TN).
U.S.A. (TN).
C* .............
5
R4 ............
C ...............
C* .............
C ...............
2
5
2
R4 ............
R4 ............
R3 ............
C* .............
C* .............
C ...............
C* .............
C ...............
C ...............
C ...............
2
5
5
2
5
11
5
C ...............
4
R3 ............
Margaritifera marrianae ....
Lexingtonia dolabelloides
Pleurobema strodeanum ..
Pleurobema hanleyanum
Fusconaia escambia ........
Quincuncina burkei ..........
Hamiota (=Lampsilis)
australis.
Cumberlandia monodonta
C* .............
2
R4 ............
Elliptio spinosa .................
R4
R4
R4
R4
R4
R4
R4
............
............
............
............
............
............
............
SNAILS
C ...............
C ...............
C* .............
2
2
9
R4 ............
R4 ............
R6 ............
C* .............
C* .............
8
2
R6 ............
R4 ............
C* .............
C* .............
2
2
R1 ............
R2 ............
C*
C*
C*
C*
C*
C*
C*
C*
C*
C*
.............
.............
.............
.............
.............
.............
.............
.............
.............
.............
2
2
2
2
2
2
2
2
2
2
R1 ............
R1 ............
R1 ............
R1 ............
R1 ............
R1 ............
R2 ............
R1 ............
R2 ............
CNO .........
C* .............
C* .............
11
2
R2 ............
R2 ............
C*
C*
C*
C*
.............
.............
.............
.............
5
11
5
2
R2
R2
R2
R2
C* .............
C* .............
2
2
Pleurocera foremani .........
Elimia melanoides ............
Oreohelix peripherica
wasatchensis.
Stagnicola bonnevillensis
Leptoxis foremani
(=downei).
Ostodes strigatus .............
Pseudotryonia
adamantina.
Samoana fragilis ..............
Partula radiolata ...............
Partula gibba ....................
Partulina semicarinata .....
Partulina variabilis ............
Partula langfordi ...............
Cochliopa texana .............
Eua zebrina ......................
Pyrgulopsis chupaderae ..
Pyrgulopsis notidicola ......
Potaridae .............
Hydrobiidae .........
Partulidae ............
Partulidae ............
Partulidae ............
Achatinellidae ......
Achatinellidae ......
Partulidae ............
Hydrobiidae .........
Partulidae ............
Hydrobiidae .........
Hydrobiidae .........
............
............
............
............
Pyrgulopsis gilae ..............
Tryonia circumstriata
(=stocktonensis).
Pyrgulopsis thompsoni .....
Pyrgulopsis thermalis .......
Pyrgulopsis morrisoni .......
Tryonia cheatumi .............
Hydrobiidae .........
Hydrobiidae .........
Hydrobiidae
Hydrobiidae
Hydrobiidae
Hydrobiidae
R2 ............
R1 ............
Pyrgulopsis trivialis ..........
Newcombia cumingi .........
Hydrobiidae .........
Achatinellidae ......
.........
.........
.........
.........
U.S.A. (AS).
U.S.A. (TX).
(GU, MP).
(GU).
(GU, MP).
(HI).
(HI).
(MP).
(TX).
(AS).
(NM).
(NV).
U.S.A. (NM).
U.S.A. (TX).
(AZ), Mexico.
(NM).
(AZ).
(TX).
U.S.A. (AZ).
U.S.A. (HI)
INSECTS
11
R6 ............
Zaitzevia thermae ............
Elmidae ...............
C* .............
C ...............
C* .............
sroberts on PROD1PC70 with PROPOSALS
C* .............
8
3
3
R1 ............
R4 ............
R1 ............
Lygaeidae ............
Nymphalidae .......
Nymphalidae .......
C* .............
2
R1 ............
Nysius wekiuicola .............
Anaea troglodyta floridalis
Hypolimnas octucula
mariannensis.
Vagrans egestina .............
C* .............
6
R4 ............
Lycaenidae ..........
C* .............
C ...............
5
5
R4 ............
R4 ............
Cyclargus thomasi
bethunebakeri.
Glyphopsyche sequatchie
Pseudanophthalmus
insularis.
VerDate Aug<31>2005
16:24 Sep 11, 2006
Jkt 208001
PO 00000
Frm 00075
Nymphalidae .......
Limnephilidae ......
Carabidae ............
Fmt 4701
Sfmt 4702
E:\FR\FM\12SEP2.SGM
12SEP2
U.S.A. (HI).
U.S.A. (FL).
U.S.A. (GU, MP).
U.S.A. (GU, MP).
U.S.A. (FL), Bahamas.
53830
Federal Register / Vol. 71, No. 176 / Tuesday, September 12, 2006 / Proposed Rules
TABLE 1.—CANDIDATE NOTICE OF REVIEW (ANIMALS AND PLANTS)—Continued
[Note: See end of SUPPLEMENTARY INFORMATION for an explanation of symbols used in this table.]
Status
Category
Lead
region
Priority
Scientific name
Family
Common name
Pseudanophthalmus
major.
Pseudanophthalmus
caecus.
Pseudanophthalmus
colemanensis.
Pseudanophthalmus
fowlerae.
Pseudanophthalmus
frigidus.
Pseudanophthalmus
tiresias.
Pseudanophthalmus inquisitor.
Pseudanophthalmus troglodytes.
Pseudanophthalmus paulus.
Pseudanophthalmus
inexpectatus.
Pseudanophthalmus
parvus.
Euphydryas editha taylori
Carabidae ............
Cave beetle, beaver .........
U.S.A. (KY).
Carabidae ............
Cave beetle, Clifton .........
U.S.A. (KY).
Carabidae ............
Cave beetle, Coleman .....
U.S.A. (TN).
Carabidae ............
Cave beetle, Fowler’s ......
U.S.A. (TN).
Carabidae ............
Cave beetle, icebox .........
U.S.A. (KY).
Carabidae ............
U.S.A. (TN).
Carabidae ............
Cave beetle, Indian Grave
Point (=Soothsayer).
Cave beetle, inquirer ........
Carabidae ............
Cave beetle, Louisville .....
U.S.A. (KY).
Carabidae ............
Cave beetle, Noblett’s ......
U.S.A. (TN).
Carabidae ............
Cave beetle, surprising ....
U.S.A. (KY).
Carabidae ............
Cave beetle, Tatum .........
U.S.A. (KY).
Nymphalidae .......
Coenagrionidae ...
Checkerspot, Taylor’s
(=Whulge).
Damselfly, blackline Hawaiian.
U.S.A. (OR, WA), Canada
(BC).
U.S.A. (HI).
Damselfly, crimson Hawaiian.
Damselfly, flying earwig
Hawaiian.
Damselfly, oceanic Hawaiian.
Damselfly, orangeblack
Hawaiian.
Damselfly, Pacific Hawaiian.
Hairstreak, Bartram’s .......
Naucorid bug (=Furnace
Creek), Nevares Spring.
fly, Picture-wing ................
fly, Picture-wing
[unnamed].
Riffle beetle, Stephan’s ....
Skipper, Dakota ...............
U.S.A. (HI).
C* .............
5
R4 ............
C* .............
5
R4 ............
C ...............
11
R4 ............
C ...............
5
R4 ............
C* .............
5
R4 ............
C ...............
5
R4 ............
C* .............
5
R4 ............
C* .............
5
R4 ............
C ...............
5
R4 ............
C* .............
11
R4 ............
C* .............
5
R4 ............
C* .............
3
R1 ............
C* .............
9
R1 ............
C* .............
2
R1 ............
Megalagrion
nigrohamatum nigrolineatum.
Megalagrion leptodemas ..
C* .............
2
R1 ............
Megalagrion nesiotes .......
Coenagrionidae ...
C* .............
2
R1 ............
Megalagrion oceanicum ...
Coenagrionidae ...
C* .............
8
R1 ............
Megalagrion xanthomelas
Coenagrionidae ...
C* .............
2
R1 ............
Megalagrion pacificum .....
Coenagrionidae ...
C ...............
C ...............
3
5
R4 ............
CNO .........
Strymon acis bartrami ......
Ambrysus funebris ...........
Lycaenidae ..........
Naucoridae ..........
C* .............
C* .............
2
2
R1 ............
R1 ............
Drosophila attigua ............
Drosophila digressa .........
Drosophilidae ......
Drosophilidae ......
C* .............
C* .............
5
11
R2 ............
R3 ............
Heterelmis stephani .........
Hesperia dacotae .............
Elmidae ...............
Hesperiidae .........
C* .............
C* .............
5
9
R1 ............
R6 ............
Hesperiidae .........
Cicindelidae .........
C* .............
5
R4 ............
Polites mardon .................
Cicindela limbata
albissima.
Cicindela highlandensis ...
Coenagrionidae ...
Cicindelidae .........
Skipper, Mardon ...............
Tiger beetle, Coral Pink
Sand Dunes.
Tiger beetle, highlands ....
Historic range
U.S.A. (TN).
U.S.A. (HI).
U.S.A. (HI).
U.S.A. (HI).
U.S.A. (HI).
U.S.A. (FL).
U.S.A. (CA).
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).
ARACHNIDS
C* .............
2
R2 ............
Cicurina wartoni ...............
Dictynidae ............
Meshweaver, Warton’s
cave.
U.S.A. (TX).
Amphipod, diminutive .......
Shrimp, anchialine pool ...
Shrimp, anchialine pool ...
Shrimp, anchialine pool ...
Shrimp, anchialine pool ...
Shrimp, troglobitic groundwater.
U.S.A. (TX).
U.S.A. (HI).
U.S.A. (HI).
U.S.A. (HI).
U.S.A. (HI).
U.S.A. (PR), Barbuda, Dominican Republic.
sroberts on PROD1PC70 with PROPOSALS
CRUSTACEANS
C ...............
C* .............
C* .............
C* .............
C* .............
C* .............
VerDate Aug<31>2005
2
5
5
5
4
5
R2
R1
R1
R1
R1
R4
............
............
............
............
............
............
16:24 Sep 11, 2006
Gammarus hyalleloides ...
Metabetaeus lohena ........
Palaemonella burnsi ........
Procaris hawaiana ...........
Vetericaris chaceorum .....
Typhlatya monae .............
Jkt 208001
PO 00000
Frm 00076
Gammaridae ........
Alpheidae ............
Palaemonidae .....
Procarididae ........
Procaridae ...........
Atyidae ................
Fmt 4701
Sfmt 4702
E:\FR\FM\12SEP2.SGM
12SEP2
Federal Register / Vol. 71, No. 176 / Tuesday, September 12, 2006 / Proposed Rules
53831
TABLE 1.—CANDIDATE NOTICE OF REVIEW (ANIMALS AND PLANTS)—Continued
[Note: See end of SUPPLEMENTARY INFORMATION for an explanation of symbols used in this table.]
Status
Category
Lead
region
Priority
Scientific name
Family
Common name
Historic range
FLOWERING PLANTS
8
CNO .........
Abronia alpina ..................
Nyctaginaceae .....
C* .............
C* .............
C* .............
8
11
3
R4 ............
R4 ............
R1 ............
C*
C*
C*
C*
.............
.............
.............
.............
2
11
2
3
R1
R6
R1
R1
C* .............
6
R1 ............
C* .............
C* .............
8
3
R1 ............
R1 ............
C*
C*
C*
C*
C*
C*
C*
C*
C*
C*
.............
.............
.............
.............
.............
.............
.............
.............
.............
.............
8
2
2
5
5
5
2
2
8
6
R4 ............
R1 ............
R1 ............
R4 ............
CNO .........
R4 ............
R1 ............
R1 ............
R1 ............
R4 ............
C* .............
12
R4 ............
C* .............
6
R4 ............
C* .............
C* .............
2
3
R1 ............
R1 ............
C* .............
3
R1 ............
C* .............
C* .............
2
6
R1 ............
CNO .........
C* .............
2
R4 ............
Arabis georgiana ..............
Argythamnia blodgettii .....
Artemisia campestris var.
wormskioldii.
Astelia waialealae ............
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 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 .....
C* .............
2
R4 ............
Consolea corallicola .........
Cactaceae ...........
C*
C*
C*
C*
C*
C*
C*
C*
C*
C*
C*
C*
C*
C*
C*
sroberts on PROD1PC70 with PROPOSALS
C* .............
.............
.............
.............
.............
.............
.............
.............
.............
.............
.............
.............
.............
.............
.............
.............
2
2
2
2
2
2
2
2
2
2
2
2
2
2
9
R4
R1
R1
R1
R1
R1
R1
R1
R1
R1
R1
R1
R1
R1
R4
Boraginaceae ......
Campanulaceae ..
Campanulaceae ..
Campanulaceae ..
Campanulaceae ..
Campanulaceae ..
Campanulaceae ..
Campanulaceae ..
Campanulaceae ..
Gesneriaceae ......
Gesneriaceae ......
Gesneriaceae ......
Gesneriaceae ......
Gesneriaceae ......
Fabaceae ............
C* .............
C* .............
5
5
R5 ............
R4 ............
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 ...........
C* .............
3
R1 ............
C* .............
3
R1 ............
C* .............
2
R1 ............
Dubautia imbricata
imbricata.
Dubautia plantaginea
magnifolia.
Dubautia waialealae .........
VerDate Aug<31>2005
............
............
............
............
............
............
............
............
............
............
............
............
............
............
............
............
............
............
............
16:24 Sep 11, 2006
Jkt 208001
PO 00000
Frm 00077
Brassicaceae .......
Euphorbiaceae ....
Asteraceae ..........
Sand-verbena, Ramshaw
Meadows.
Rockcress, Georgia .........
Silverbush, Blodgett’s ......
Wormwood, northern .......
U.S.A. (AL, GA).
U.S.A. (FL).
U.S.A. (OR, WA).
Liliaceae ..............
Fabaceae ............
Asteraceae ..........
Asteraceae ..........
Pa1iniu ...............................
Milk-vetch, Sleeping Ute ..
Ko1oko1olau .......................
Ko1oko1olau .......................
U.S.A.
U.S.A.
U.S.A.
U.S.A.
Asteraceae ..........
Ko1oko1olau .......................
U.S.A. (HI).
Asteraceae ..........
Asteraceae ..........
Ko1oko1olau .......................
Ko1oko1olau .......................
U.S.A. (HI).
U.S.A. (HI).
Asteraceae ..........
Poaceae ..............
Poaceae ..............
Mimosaceae ........
Liliaceae ..............
Myrtaceae ............
Fabaceae ............
Fabaceae ............
Scrophulariaceae
Fabaceae ............
Brickell-bush, Florida .......
No common name ...........
No common name ...........
No common name ...........
Mariposa lily, Siskiyou .....
No common name ...........
1Awikiwiki ..........................
1Awikiwiki ..........................
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.
Euphorbiaceae ....
Sandmat, pineland ...........
U.S.A. (FL).
Euphorbiaceae ....
Spurge, wedge .................
U.S.A. (FL).
Euphorbiaceae ....
Euphorbiaceae ....
1Akoko ...............................
1Akoko ..............................
U.S.A. (HI).
U.S.A. (HI).
Euphorbiaceae ....
1Akoko ..............................
U.S.A. (HI).
Amaranthaceae ...
Polygonaceae ......
Papala ..............................
Spineflower, San Fernando Valley.
Thoroughwort, Cape
Sable.
Cactus, Florida semaphore.
No common name ...........
Haha .................................
Haha .................................
Haha .................................
Haha .................................
Haha .................................
Haha .................................
Haha .................................
Aku ...................................
Ha1iwale ............................
Ha1iwale ............................
Ha1iwale ............................
Ha1iwale ............................
Ha1iwale ............................
Prairie-clover, Florida .......
U.S.A. (HI).
U.S.A. (CA).
Asteraceae ..........
Poaceae ..............
Poaceae ..............
U.S.A. (CA).
(HI).
(CO).
(HI).
(HI).
(FL).
(HI).
(HI).
(PR).
(CA, OR).
(PR).
(HI).
(HI).
(ID).
(FL).
U.S.A. (FL).
U.S.A. (FL).
U.S.A.
U.S.A.
U.S.A.
U.S.A.
U.S.A.
U.S.A.
U.S.A.
U.S.A.
U.S.A.
U.S.A.
U.S.A.
U.S.A.
U.S.A.
U.S.A.
U.S.A.
(PR), Anegada.
(HI).
(HI).
(HI).
(HI).
(HI).
(HI).
(HI).
(HI).
(HI).
(HI).
(HI).
(HI).
(HI).
(FL).
U.S.A. (DE, GA, NC, NJ).
U.S.A. (FL).
Asteraceae ..........
Panic grass, Hirsts’ ..........
Crabgrass, Florida pineland.
Na1ena1e ...........................
Asteraceae ..........
Na1ena1e ...........................
U.S.A. (HI).
Asteraceae ..........
Na1ena1e ...........................
U.S.A. (HI).
Fmt 4701
Sfmt 4702
E:\FR\FM\12SEP2.SGM
12SEP2
U.S.A. (HI).
53832
Federal Register / Vol. 71, No. 176 / Tuesday, September 12, 2006 / Proposed Rules
TABLE 1.—CANDIDATE NOTICE OF REVIEW (ANIMALS AND PLANTS)—Continued
[Note: See end of SUPPLEMENTARY INFORMATION for an explanation of symbols used in this table.]
Status
Category
Lead
region
Priority
Scientific name
Family
Common name
Cactaceae ...........
Cactus, Acuna ..................
U.S.A. (AZ), Mexico.
Asteraceae ..........
Asteraceae ..........
Polygonaceae ......
U.S.A. (AZ).
U.S.A. (WA).
U.S.A. (WA).
Historic range
6
R2 ............
C* .............
C* .............
C* .............
8
11
2
R2 ............
R1 ............
R1 ............
Echinomastus
erectocentrus var.
acunensis.
Erigeron lemmonii ............
Erigeron basalticus ..........
Eriogonum codium ...........
C ...............
2
CNO .........
Eriogonum diatomaceum
Polygonaceae ......
C* .............
C* .............
C* .............
C* .............
C* .............
C* .............
C* .............
C* .............
C ...............
5
2
11
2
5
8
5
5
5
CNO .........
R1 ............
R2 ............
R1 ............
R1 ............
R1 ............
R1 ............
R4 ............
R4 ............
Eriogonum kelloggii ..........
Festuca hawaiiensis .........
Festuca ligulata ................
Gardenia remyi ................
Geranium hanaense ........
Geranium hillebrandii .......
Geranium kauaiense ........
Gonocalyx concolor .........
Harrisia aboriginum ..........
Polygonaceae ......
Poaceae ..............
Poaceae ..............
Rubiaceae ...........
Geraniaceae ........
Geraniaceae ........
Geraniaceae ........
Ericaceae ............
Cactaceae ...........
C*
C*
C*
C*
.............
.............
.............
.............
5
2
11
5
CNO .........
R1 ............
R4 ............
R2 ............
Hazardia orcuttii ...............
Hedyotis fluviatilis ............
Helianthus verticillatus .....
Hibiscus dasycalyx ...........
Asteraceae ..........
Rubiaceae ...........
Asteraceae ..........
Malvaceae ...........
C* .............
9
R4 ............
Fabaceae ............
2
5
3
R6 ............
CNO .........
R1 ............
Polemoniaceae ....
Rosaceae ............
Joinvilleaceae ......
Skyrocket, Pagosa ...........
Ivesia, Webber .................
1Ohe ..................................
U.S.A. (CO).
U.S.A. (CA, NV).
U.S.A. (HI).
C* .............
2
R1 ............
Asteraceae ..........
No common name ...........
U.S.A. (HI).
C* .............
2
R1 ............
Asteraceae ..........
No common name ...........
U.S.A. (HI).
C*
C*
C*
C*
C*
C*
C*
C*
.............
.............
.............
.............
.............
.............
.............
.............
2
2
2
5
2
5
2
3
R1
R1
R1
R4
R2
R4
R4
R4
............
............
............
............
............
............
............
............
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 .........
Linum arenicola ................
Linum carteri var. carteri ..
Fleabane, Lemmon ..........
Daisy, basalt ....................
Buckwheat, Umtanum
Desert.
Buckwheat, Churchill Narrows.
Buckwheat, Red Mountain
No common name ...........
Guadalupe fescue ............
Nanu .................................
Nohoanu ...........................
Nohoanu ...........................
Nohoanu ...........................
No common name ...........
Pricklyapple, aboriginal
(shell mound
applecactus).
Orcutt’s hazardia ..............
Kampua1a .........................
Sunflower, whorled ..........
Rose-mallow, Neches
River.
Indigo, Florida ..................
C ...............
C* .............
C* .............
Viscaceae ............
Loganiaceae ........
Loganiaceae ........
Brassicaceae .......
Brassicaceae .......
Brassicaceae .......
Linaceae ..............
Linaceae ..............
.............
.............
.............
.............
.............
.............
.............
.............
.............
.............
.............
2
2
2
2
2
2
2
2
2
2
8
R1
R1
R1
R1
R1
R1
R1
R1
R1
R1
R5
............
............
............
............
............
............
............
............
............
............
............
Lysimachia daphnoides ...
Melicope christophersenii
Melicope degeneri ............
Melicope hiiakae ..............
Melicope makahae ...........
Melicope paniculata .........
Melicope puberula ............
Myrsine fosbergii ..............
Myrsine mezii ...................
Myrsine vaccinioides ........
Narthecium americanum ..
Primulaceae ........
Rutaceae .............
Rutaceae .............
Rutaceae .............
Rutaceae .............
Rutaceae .............
Rutaceae .............
Myrsinaceae ........
Myrsinaceae ........
Myrsinaceae ........
Liliaceae ..............
Hulumoa ...........................
Kamakahala .....................
Kamakahala .....................
Gladecress, unnamed ......
Gladecress, Texas golden
Bladderpod, Short’s .........
Flax, sand ........................
Flax, Carter’s small-flowered.
Lehua makanoe ...............
Alani .................................
Alani .................................
Alani .................................
Alani .................................
Alani .................................
Alani .................................
Kolea ................................
Kolea ................................
Kolea ................................
Asphodel, bog ..................
U.S.A.
U.S.A.
U.S.A.
U.S.A.
U.S.A.
U.S.A.
U.S.A.
U.S.A.
C*
C*
C*
C*
C*
C*
C*
C*
C*
C*
C*
C* .............
C* .............
C* .............
sroberts on PROD1PC70 with PROPOSALS
C* .............
2
2
3
R1 ............
R1 ............
R2 ............
Solanaceae .........
Apocynaceae .......
Cactaceae ...........
1Aiea .................................
Holei .................................
Cactus, Fickeisen plains ..
C* .............
PT ............
C* .............
2
2
6
R6 ............
R6 ............
R6 ............
Scrophulariaceae
Scrophulariaceae
Scrophulariaceae
Beardtongue, Parachute ..
Beardtongue, Graham .....
Beardtongue, White River
U.S.A. (CO).
U.S.A. (CO, UT).
U.S.A. (CO, UT).
C* .............
C ...............
C* .............
C* .............
C* .............
2
2
8
2
2
R1 ............
CNO .........
R6 ............
R1 ............
R1 ............
Nothocestrum latifolium ...
Ochrosia haleakalae ........
Pediocactus peeblesianus
fickeiseniae.
Penstemon debilis ............
Penstemon grahamii ........
Penstemon scariosus var.
albifluvis.
Peperomia subpetiolata ...
Phacelia stellaris ..............
Phacelia submutica ..........
Phyllostegia bracteata ......
Phyllostegia floribunda .....
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. (AZ).
Piperaceae ..........
Hydrophyllaceae ..
Hydrophyllaceae ..
Lamiaceae ...........
Lamiaceae ...........
1Ala 1ala wai nui ................
Brand’s phacelia ..............
Phacelia, DeBeque ..........
No common name ...........
No common name ...........
U.S.A.
U.S.A.
U.S.A.
U.S.A.
U.S.A.
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12SEP2
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.
U.S.A.
U.S.A.
(CA).
(HI).
(TX), Mexico.
(HI).
(HI).
(HI).
(HI).
(PR).
(FL)
U.S.A.
U.S.A.
U.S.A.
U.S.A.
(CA), Mexico.
(HI).
(AL, GA, TN).
(TX).
U.S.A. (FL).
(HI).
(HI).
(HI).
(AL).
(TX).
(IN, KY, TN).
(FL).
(FL).
(HI).
(CA), Mexico.
(CO).
(HI).
(HI).
Federal Register / Vol. 71, No. 176 / Tuesday, September 12, 2006 / Proposed Rules
53833
TABLE 1.—CANDIDATE NOTICE OF REVIEW (ANIMALS AND PLANTS)—Continued
[Note: See end of SUPPLEMENTARY INFORMATION for an explanation of symbols used in this table.]
Status
Category
Lead
region
Priority
Scientific name
Family
Common name
Phyllostegia hispida .........
Physaria (=Lesquerella)
tuplashensis.
Pittosporum napaliense ...
Platanthera integrilabia ....
Lamiaceae ...........
Brassicaceae .......
No common name ...........
Bladderpod, White Bluffs
U.S.A. (HI).
U.S.A. (WA).
Pittosporaceae ....
Orchidaceae ........
Ho1awa .............................
Orchid, white fringeless ...
Platydesma cornuta var.
cornuta.
Platydesma cornuta var.
decurrens.
Platydesma remyi ............
Platydesma rostrata .........
Pleomele fernaldii ............
Pleomele forbesii .............
Potentilla basaltica ...........
Rutaceae .............
No common name ...........
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 ............
U.S.A.
U.S.A.
U.S.A.
U.S.A.
U.S.A.
Pritchardia hardyi .............
Pseudognaphalium
(=Gnaphalium)
sandwicensium var.
molokaiense.
Psychotria grandiflora ......
Psychotria hexandra ssp.
oahuensis var.
oahuensis.
Psychotria hobdyi .............
Pteralyxia macrocarpa .....
Ranunculus hawaiensis ...
Ranunculus mauiensis .....
Rorippa subumbellata ......
Schiedea attenuata ..........
Schiedea pubescens ........
Schiedea salicaria ............
Sedum eastwoodiae ........
Sicyos macrophyllus ........
Sideroxylon reclinatum
ssp. austrofloridense.
Solanum nelsonii ..............
Solidago plumosa ............
Stenogyne cranwelliae .....
Stenogyne kealiae ...........
Symphyotrichum
georgianum.
Zanthoxylum oahuense ....
Asteraceae ..........
Asteraceae ..........
No common name ...........
Pilo kea lau li1i ..................
Hala pepe .........................
Hala pepe .........................
Cinquefoil, Soldier Meadow.
Lo1ulu ................................
1Ena1ena ...........................
Rubiaceae ...........
Rubiaceae ...........
Kopiko ..............................
Kopiko ..............................
U.S.A. (HI).
U.S.A. (HI).
Rubiaceae ...........
Apocynaceae .......
Ranunculaceae ...
Ranunculaceae ...
Brassicaceae .......
Caryophyllaceae ..
Caryophyllaceae ..
Caryophyllaceae ..
Crassulaceae ......
Cucurbitaceae .....
Sapotaceae .........
Kopiko ..............................
Kaulu ................................
Makou ..............................
Makou ..............................
Cress, Tahoe yellow ........
No common name ...........
Ma1oli1oli ............................
No common name ...........
Stonecrop, Red Mountain
1Anunu ..............................
Bully, Everglades .............
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.
Solanaceae .........
Asteraceae ..........
Lamiaceae ...........
Lamiaceae ...........
Asteraceae ..........
Popolo ..............................
Goldenrod, Yadkin River ..
No common name ...........
No common name ...........
Aster, Georgia ..................
Rutaceae .............
A1e ....................................
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).
C* .............
C* .............
2
5
R1 ............
R1 ............
C* .............
C* .............
2
5
R1 ............
R4 ............
C* .............
3
R1 ............
C* .............
3
R1 ............
C* .............
C* .............
C ...............
C* .............
C* .............
2
2
2
2
11
R1 ............
R1 ............
R1 ............
R1 ............
CNO .........
C* .............
C* .............
2
3
R1 ............
R1 ............
C* .............
C* .............
2
3
R1 ............
R1 ............
C* .............
C* .............
C* .............
C* .............
C* .............
C* .............
C* .............
C* .............
C* .............
C* .............
C ...............
2
2
2
2
8
2
2
2
5
2
9
R1 ............
R1 ............
R1 ............
R1 ............
CNO .........
R1 ............
R1 ............
R1 ............
CNO .........
R1 ............
R4 ............
C* .............
C ...............
C* .............
C* .............
C* .............
2
8
2
2
5
R1
R4
R1
R1
R4
C* .............
2
R1 ............
............
............
............
............
............
Historic range
(HI).
(HI).
(HI).
(HI).
(NV).
U.S.A. (HI).
U.S.A. (HI).
(HI).
(HI).
(HI).
(HI).
(CA, NV).
(HI).
(HI).
(HI).
(CA).
(HI).
(FL).
FERNS AND ALLIES
11
R1 ............
Botrychium lineare ...........
Ophioglossaceae
Moonwort, slender ...........
C* .............
2
R1 ............
Thelypteridaceae
No common name ...........
2
2
R1 ............
R1 ............
Pteridaceae .........
Lycopodiaceae ....
No common name ...........
Wawae1iole .......................
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).
C* .............
C* .............
sroberts on PROD1PC70 with PROPOSALS
C* .............
Dennstaedtiaceae
Palapali ............................
U.S.A. (HI).
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53834
Federal Register / Vol. 71, No. 176 / Tuesday, September 12, 2006 / Proposed Rules
TABLE 2.—ANIMALS AND PLANTS FORMERLY CANDIDATES OR FORMERLY PROPOSED FOR LISTING
[Note: See end of SUPPLEMENTARY INFORMATION for an explanation of symbols used in this table.]
Status
Code
Expl.
Lead
region
Scientific name
Family
Common name
Historical range
MAMMALS
T ...............
L ...............
R7 ............
Enhydra lutris kenyoni .......
Mustelidae ...
Otter, Northern Sea (southwest Alaska DPS).
U.S.A. (AK, WA).
BIRDS
Rc .............
A ..............
R6 ............
Centrocercus minimus .......
Phasianidae
Sage-grouse, Gunnison .....
Rc .............
A ..............
R1 ............
Ptilinopus perousii perousii
Columbidae ..
Fruit-dove, many-colored ...
U.S.A. (AZ, CO, KS, OK,
NM, UT).
U.S.A. (AS), Independent
Samoa.
Turtle, Cagle’s map ...........
U.S.A. (TX).
Toad, boreal (Southern
Rocky Mountains DPS).
U.S.A. (AK, CA, CO, ID,
MT, NM, OR, UT, WA,
WY), Canada (BC).
Chub, Gila ..........................
U.S.A. (AZ, NM), Mexico.
Snail, Koster’s tryonia ........
Snail, Pecos assiminea .....
Springsnail, Roswell ..........
U.S.A. (NM).
U.S.A. (NM, TX), Mexico.
U.S.A. (NM).
U.S.A. (KY).
U.S.A. (HI).
U.S.A. (HI). wing
[unnamed]
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. (NE).
REPTILES
Rc .............
A ..............
R2 ............
Graptemys caglei ...............
Emydidae .....
AMPHIBIANS
Rc .............
N ..............
R6 ............
Bufo boreas boreas ...........
Bufonidae .....
FISHES
E ...............
L ..............
R2 ............
Gila intermedia ...................
Cyprinidae ....
SNAILS
E ...............
E ...............
E ...............
L ..............
L ..............
L ..............
R2 ............
R2 ............
R2 ............
Tryonia kosteri ...................
Assiminea pecos ................
Pyrgulopsis roswellensis ....
Hydrobiidae ..
Assimineidae
Hydrobiidae ..
INSECTS
Rc .............
U ..............
R4 ............
Rc .............
U ..............
R4 ............
Rc .............
E ...............
I ...............
L ..............
R1 ............
R1 ............
E
E
E
E
T
E
E
E
E
E
E
E
L
L
L
L
L
L
L
L
L
L
L
L
R1
R1
R1
R1
R1
R1
R1
R1
R1
R1
R1
R6
...............
...............
...............
...............
...............
...............
...............
...............
...............
...............
...............
...............
..............
..............
..............
..............
...............
..............
..............
..............
..............
..............
..............
..............
............
............
............
............
............
............
............
............
............
............
............
............
Pseudanophthalmus
pholete.
Pseudanophthalmus
cataryctos.
Phaeogramma sp. .............
Drosophila aglaia ...............
Carabidae ....
Carabidae ....
Cave beetle, greater
Adams.
Cave beetle, lesser Adams
Tephritidae ...
Drosophilidae
Gall fly, Po‘olanui ...............
fly, Picture ..........................
Drosophila differens ...........
Drosophila hemipeza .........
Drosophila heteroneura .....
Drosophila montgomeryi ....
Drosophila mulli .................
Drosophila musaphila ........
Drosophila neoclavisetae ...
Drosophila obatai ...............
Drosophila ochrobasis .......
Drosophila substenoptera ..
Drosophila tarphytrichia .....
Cicindela nevadica
lincolniana.
Drosophilidae
Drosophilidae
Drosophilidae
Drosophilidae
Drosophilidae
Drosophilidae
Drosophilidae
Drosophilidae
Drosophilidae
Drosophilidae
Drosophilidae
Cicindelidae
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]
Tiger beetle, Salt Creek .....
U.S.A. (KY).
CRUSTACEANS
L ..............
I ...............
R2 ............
R1 ............
Gammarus desperatus ......
Antecaridina lauensis .........
Gammaridae
Atyidae .........
Amphipod, Noel’s ...............
Shrimp, anchialine pool .....
Rc .............
sroberts on PROD1PC70 with PROPOSALS
E ...............
Rc .............
I ...............
R1 ............
Calliasmata pholidota ........
Alpheidae .....
Shrimp, anchialine pool .....
U.S.A. (NM).
U.S.A. (HI), Mozambique,
Saudi Arabia, Japan.
U.S.A. (HI), Funafuti Atoll,
Saudi Arabia, Sinai Peninsula, Tuvalu.
Alice-flower, wonderland ....
U.S.A. (UT).
Milk-vetch, horseshoe ........
U.S.A. (UT).
FLOWERING PLANTS
Rc .............
A ..............
R6 ............
Aliciella cespitosa ..............
Rc .............
A ..............
R6 ............
Astragalus equisolensis .....
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Polemoniaceae.
Fabaceae .....
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Federal Register / Vol. 71, No. 176 / Tuesday, September 12, 2006 / Proposed Rules
53835
TABLE 2.—ANIMALS AND PLANTS FORMERLY CANDIDATES OR FORMERLY PROPOSED FOR LISTING—Continued
[Note: See end of SUPPLEMENTARY INFORMATION for an explanation of symbols used in this table.]
Status
Family
Common name
Expl.
Lead
region
Scientific name
Code
Rc .............
A ..............
R6 ............
Castilleja aquariensis .........
Paintbrush, Aquarius .........
U.S.A. (UT).
Rc .............
I ...............
R2 ............
Paronychia congesta .........
Whitlow-wort, bushy ...........
U.S.A. (TX).
Rc .............
A ..............
CNO .........
Sidalcea hickmanii parishii
Scrophulariaceae.
Caryophyllaceae.
Malvaceae ...
Checkerbloom, Parish’s .....
U.S.A. (CA).
[FR Doc. 06–7375 Filed 9–11–06; 8:45 am]
sroberts on PROD1PC70 with PROPOSALS
BILLING CODE 4310–55–P
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Historical range
Agencies
[Federal Register Volume 71, Number 176 (Tuesday, September 12, 2006)]
[Proposed Rules]
[Pages 53756-53835]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 06-7375]
[[Page 53755]]
-----------------------------------------------------------------------
Part II
Department of the Interior
-----------------------------------------------------------------------
Fish and Wildlife Service
-----------------------------------------------------------------------
50 CFR Part 17
Endangered and Threatened Wildlife and Plants--Proposed Critical
Habitat Designations; Proposed Rule
Federal Register / Vol. 71, No. 176 / Tuesday, September 12, 2006 /
Proposed Rules
[[Page 53756]]
-----------------------------------------------------------------------
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.
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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 landowners and resource managers to alleviate threats and
thereby possibly remove the need to list species as endangered or
threatened. Even if we subsequently list a candidate species, the early
notice provided here could result in more options for species
management and recovery by prompting candidate conservation measures to
alleviate threats to the species.
The CNOR summarizes the status and threats that we evaluated in
order to determine that species qualify as candidates and to assign a
listing priority number to each species, or to remove species from
candidate status. Additional material that we relied on is available in
the Species Assessment and Listing Priority Assignment Forms (species
assessment forms, previously called candidate forms) for each candidate
species.
Overall, this CNOR recognizes 7 new candidates, changes the listing
priority number for 24 candidates, and removes 10 species from
candidate status. Combined with other decisions for individual species
that were published separately from this CNOR, the new number of
species that are candidates for listing is 279.
We request additional status information that may be available for
the 279 candidate species identified in this CNOR. We will consider
this information in preparing listing documents and future revisions to
the notice of review, as it will help us in monitoring changes in the
status of candidate species and in management for conserving them. We
also request information on additional species that we should consider
including as candidates as we prepare future updates of this notice.
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 2, 2005, through
August 23, 2006.
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. As defined in section 3 of the
Act, an endangered species is any species which is in danger of
extinction throughout all or a significant portion of its range, and a
threatened species is any species which is likely to become an
endangered species within the foreseeable future throughout all or a
significant portion of its range. Through the Federal rulemaking
process, we add species that meet these definitions to the List of
Endangered and Threatened Wildlife at 50 CFR 17.11 or the List of
Endangered and Threatened Plants at 50 CFR 17.12. As part of this
program, we maintain a list of species that we regard as candidates for
listing. A candidate species is one for which we have on file
sufficient information on biological vulnerability and threats to
support a proposal to list as endangered or threatened, but for which
preparation and publication of a proposal is precluded by higher-
priority listing actions.
We maintain this list of candidates for a variety of reasons: To
notify the public that these species are facing threats to their
survival; to provide advance knowledge of potential listings that could
affect decisions of environmental planners and developers; to provide
information that may stimulate and guide conservation efforts that will
remove or reduce threats to these species and possibly make listing
unnecessary; to 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. We strongly encourage collaborative
conservation efforts for candidate species and offer technical and
financial assistance to facilitate such efforts. For additional
information regarding such assistance, please contact the appropriate
Regional Office listed in SUPPLEMENTARY INFORMATION or visit our
Internet Web site, https://endangered.fws.gov/candidates/.
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
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,
referring to them as species considered to be candidate endangered
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or threatened species. We published a new comprehensive notice of
review for native plants on December 15, 1980 (45 FR 82479), which took
into account the earlier Smithsonian report and other accumulated
information. On November 28, 1983 (48 FR 53640), our 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); May 4, 2004 (69 FR 24876); and May 11, 2005 (70
FR 24870). 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 (i.e. vertebrate and invertebrate) animal notice
of review on January 6, 1989 (54 FR 554), with minor corrections on
August 10, 1989 (54 FR 32833). We again published comprehensive animal
notices on November 21, 1991 (56 FR 58804) and November 15, 1994 (59 FR
58982). Beginning in 1996 we published combined animal and plant
notices, including those published 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); May 4,
2004 (69 FR 24876); and May 11, 2005 (70 FR 24870). 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.
On September 21, 1983, we published guidance for assigning a
listing priority number (LPN) for each candidate species (48 FR 43098).
We continue to use this guidance to assign each candidate a LPN of 1 to
12, depending on the magnitude of threats, imminence of threats, and
taxonomic status. Such a priority ranking guidance system is required
under section 4(h)(3) of the Act (15 U.S.C. 1533(h)(3)).
This revised notice supersedes all previous animal, plant, and
combined notices of review.
Summary of This CNOR
Since publication of the 2004 CNOR on May 11, 2005 (70 FR 24870),
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 number assigned to each species. We also
evaluated the need to emergency-list any of these species, particularly
species with high priorities (i.e. species with listing priority
numbers of 1, 2, or 3). This review and reevaluation ensures that we
focus conservation efforts on those species at greatest risk. In
addition to reviewing candidate species, the Service has worked on
numerous findings in response to petitions to list species and has
prepared proposed and final determinations for rules to list species
under the Act; some of these findings and determinations have been
completed and published in the Federal Register while work on others is
still underway (see Preclusion and Expeditious Progress, below, for
details). Since publication of the CNOR last year the Service has
completed and published final rules listing 2 species as endangered and
17 species as threatened; reviewed the status of and published findings
that listing proposals are not warranted for 4 species; and published
proposed rules for listing for 3 species for which final determinations
are pending.
Based on our review of the best available scientific and commercial
information, this CNOR identifies 7 new candidate species (see New
Candidates, below), changes the listing priority number for 24
candidates (see Listing Priority Changes in Candidates, below) and
determined that listing proposals are not warranted for an additional
10 species and thus have removed them from candidate status (see
Candidate Removals, below). Combined with the other decisions published
separately from this CNOR for individual species that previously were
candidates, a total of 279 species, including 140 plant and 139 animal
species, are now candidates awaiting preparation of rules proposing
their listing. These 279 species, along with the 3 species currently
proposed for listing, are included in Table 1.
Table 2 includes 33 species identified in the previous CNOR as
either proposed for listing or classified as candidates that are no
longer in those categories. This includes the 19 species we listed as
threatened or endangered since the previous CNOR and the 4 species for
which we published separate findings that listing is not warranted,
plus the 10 species that we have determined do not warrant preparation
of a rule to propose listing and therefore have removed from candidate
status in this CNOR.
New Candidates
Below we present brief summaries of seven new candidates that we
are recognizing in this CNOR, including one species of mammal, one
bird, two snails, two insects, and one plant. 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/). For each of these seven
species, we find that we have on file sufficient information on
biological vulnerability and threats to support a proposal to list as
endangered or threatened, but that preparation and publication of a
proposal is precluded by higher-priority listing actions (i.e. these
meet our definition of a candidate species). Two of these seven species
were petitioned for listing, and for those two species this constitutes
our finding, as required pursuant to section 4(b)(3)(B)(iii) of the
Act, 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, and that expeditious progress is being made to add
qualified species to the lists of threatened and endangered species and
to remove from such lists species for which the protections of the Act
are no longer necessary. (Additional information is provided in the
sections entitled Petition Findings and Preclusion and Expeditious
Progress, below). We also note below that one other species, a fish,
was identified as a candidate earlier this year in a separate finding
published in the Federal Register.
Mammals
New England cottontail (Sylvilagus transitionalis)--The following
summary is based on information from our files and information
collected during the public comment period on our 90-day petition
finding. On August 30, 2000, we received a petition to list this
species. We published our 90-day finding on June 30, 2004 (69 FR
39395).
The New England cottontail (NEC) is a medium- to large-sized
cottontail rabbit that may reach 1,000 grams in weight, and is one of
two species within
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the genus Sylvilagus occurring in New England. New England cottontails
are considered habitat specialists, in so far as they are dependent
upon early-successional habitats typically described as thickets. The
species is the only endemic cottontail in New England.
Historically, the NEC ranged from southeastern New York (east of
the Hudson River) north through the Champlain Valley, southern Vermont,
the southern half of New Hampshire, southern Maine, and south
throughout Massachusetts, Connecticut, and Rhode Island. The species is
now considered to be extirpated from Vermont, the current range
elsewhere has declined substantially, and occurrences have become
increasingly separated. The species' current distribution is fragmented
into five apparently isolated metapopulations in about 14 percent of
the species' historical range. The range has contracted from
approximately 90,000 sq km to 12,180 sq km, and much of the suitable
habitat within the current range is in small patches that are not
occupied by the NEC. A multi-state, regional inventory conducted in
2001-2004 found New England cottontails were absent from 93% of
approximately 2,300 habitat patches within the recent historical range
(1990 to present) that were searched for the presence of the species.
Many of the occupied sites were quite small (3 acres or less) and are
considered by some researchers to be population ``sinks.'' It is
estimated that less than one-third of the occupied sites occur on lands
in conservation status, and fewer than 10 percent of these sites in
conservation status are being managed for early successional forest
species such as the NEC.
The primary threat to the New England cottontail is ongoing
destruction and modification of its remaining habitat through natural
succession processes and through alteration related to human
development and other activities. Isolation of occupied patches of
habitat by areas of unsuitable habitat, as well as predation, appears
to be resulting in local extirpation of New England cottontails from
small patches. Based on current land uses in the region, the loss of
about 2 percent of its current range per year is expected to continue.
Additional threats include competition for food and habitat with
introduced eastern cottontails and large numbers of native white-tailed
deer, and inadequate regulatory mechanisms in effect to protect the
habitat. Based on threats of high magnitude that are imminent, we
assigned this species a listing priority number of 2. (See also the
section entitled Petition Findings, below)
Birds
Red knot (Calidris canutus rufa)--The following summary is based on
information from our files and information provided by petitioners. We
received one petition on August 9, 2004, and two others were each
received on August 5, 2005.
The rufa subspecies is one of six recognized subspecies of red knot
and one of three subspecies occurring in North America (hereafter all
mention of red knot refers strictly to the rufa subspecies). This
subspecies makes one of the longest distance migrations known in the
animal kingdom as it travels between breeding areas in the central
Canadian Arctic and wintering areas that are primarily in southern
South America along the coast of Chile and Argentina. They migrate
along the Atlantic coast of the United States (U.S.), where they may be
found from Maine to Florida. The Delaware Bay area (in Delaware and New
Jersey) is the largest known spring migration stopover area, with far
fewer migrants congregating elsewhere along the Atlantic coast. The
concentration in the Delaware Bay area occurs from the middle of May to
early June, corresponding to the spawning season of horseshoe crabs.
The knots feed on horseshoe crab eggs, rebuilding energy reserves
needed to complete migration to the Arctic and arrive on the breeding
grounds in good condition.
Surveys at wintering areas and at Delaware Bay during spring
migration indicate a substantial decline in recent years. At the
Delaware Bay area, peak counts between 1982 and 1998 were as high as
95,360 knots. Although counts may vary considerably between years, some
of the population fluctuations can be attributed to predator-prey
cycles in the breeding grounds, and counts show that knots rebound from
such reductions. In the past, horseshoe crab eggs were so numerous that
a knot could eat enough in two to three weeks to double its weight.
Research shows that from 1997 to 2002 an increasing proportion of red
knots leaving the Delaware Bay failed to achieve threshold departure
masses needed to fly to breeding grounds and survive an initial few
days of snow cover, and this corresponded to reduced annual survival
rates. Recently, peak counts at the Delaware Bay area have been lower
than in the past and do not show a rebound. The peaks were 13,315 in
2004, 15,345 in 2005, and 13,455 in 2006. Counts in recent years at the
principal wintering areas in South America also are substantially lower
than in the past and do not show a rebound.
The primary factor threatening the red knot is destruction and
modification of its habitat, particularly the reduction in key food
resources resulting from reductions in horseshoe crabs, which are
harvested primarily for use as bait and secondarily to support a
biomedical industry. Commercial harvest increased substantially in the
1990's. Since 1999, a series of timing restrictions and substantially
lower harvest quotas have been adopted by the Atlantic States Marine
Fisheries Commission (ASMFC), as well as New Jersey and Delaware. In
May 2006, the ASMFC adopted restrictions effective from October 1, 2006
to September 30, 2008, including a prohibition on harvest and landing
of horseshoe crabs in New Jersey and Delaware from January 1 through
June 7, harvest of males only from June 8 through December 31, and
harvest limited to no more than 100,000 horseshoe crabs per state per
year. The ASMFC also adopted other restrictions applicable to Maryland
and Virginia. New Jersey has established restrictions which supersede
those of the ASMFC; as a result there is a moratorium on all horseshoe
crab harvest in New Jersey from May 15, 2006 through June 7, 2008,
after which the restrictions adopted by ASMFC apply.
The reductions in commercial harvest since 1999 are substantial:
726,660 horseshoe crab landings for bait were reported in 1999 in
Delaware and New Jersey, compared to 173,777 in 2004. However, we do
not know whether horseshoe crab populations will rebuild or how long a
lag time there may be in increased availability of eggs, as they need
8-10 years to reach sexual maturity and other key information for
estimating population response is lacking. A survey in Delaware Bay
showed spawning activity was stable or slightly declining from 1999 to
2004. In 2004, availability of horseshoe crab eggs on principal
shorebird foraging beaches increased over recent years. The peak number
of migrant red knots observed at Delaware Bay increased slightly in
2005 compared to 2004, and in 2006 the peak count was similar to that
in 2004. Also, body weights of red knots at the time of departure from
Delaware Bay improved in 2005 over previous years. Counts of red knots
at key wintering areas in South America, although much reduced from the
past, were similar in 2006 to the counts in 2005. Thus in recent years
the number of knots has been much lower than in the past and the trend
in the abundance is not improving despite
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a four-fold reduction in horseshoe crab landings since the late 1990's.
Other identified threat factors include habitat destruction due to
beach erosion and various shoreline protection and stabilization
projects that are impacting areas used by migrating knots for foraging,
the inadequacy of existing regulatory mechanisms, human disturbance,
and competition with other species for limited food resources. Also,
the concentration of red knots in the Delaware Bay area and at a
relatively small number of wintering areas make the species vulnerable
to potential large-scale events in those areas such as large oil spills
or severe weather.
Overall, we conclude that the threats, in particular the
modification of habitat through harvesting of horseshoe crabs to such
an extent that it puts the viability of the knot at substantial risk,
are of a high magnitude, but are nonimminent because of reductions and
restrictions on harvesting horseshoe crabs. Accordingly, we assigned a
listing priority number of 6 to this subspecies. (See also the section
entitled Petition Findings, below)
Fish
Headwater chub (Gila nigra)--We previously announced candidate
status for this species in a separate warranted-but-precluded 12-month
petition finding, published on May 3, 2006 (71 FR 26007).
Snails
Black mudalia (Elimia melanoides)--The following summary is based
on information in our files. The historical and current range of the
black mudalia, an aquatic snail, is in Alabama. The historical range
included much of the upper half of the Black Warrior River drainage,
including the main stem Black Warrior above Tuscaloosa, as well as the
Sipsey Fork and Locust Fork. The black mudalia is currently known from
five localized shoals in an approximately 30-mile reach of the upper
Locust Fork of the Black Warrior River, and from two shoals in a 1-mile
reach of the Blackburn Fork of the Little Warrior River, a tributary of
the Locust Fork. The black mudalia requires flowing water, and the
construction of two major dams on the main stem Black Warrior River
above the Fall Line (Oliver Lock and Dam, 1940; Holt Dam, 1966) and
another dam on the lower Sipsey Fork (Bankhead Dam, 1975), impounded
much of the species' historical habitat. Dams eliminate or reduce
currents within impounded areas, allowing sediments to accumulate on
inundated channel habitats. Impounded waters also experience changes in
water chemistry that can affect survival or reproduction of black
mudalia.
The primary threats to the black mudalia in the areas it currently
occupies involve habitat destruction and modification, particularly in
relation to poor water quality and habitat deterioration. Point-source
discharges and surface runoff cause nutrification, decreased dissolved
oxygen concentration, increased acidity and conductivity, and other
changes in water chemistry which are likely to seriously affect aquatic
snails. Pollution from surface runoff can originate from a wide array
of land use activities, and may include sediments, fertilizers,
herbicides, pesticides, animal wastes, septic tank and gray water
leakage, and oils and greases. Land uses in the vicinity of black
mudalia populations include pasture, row crops, timber production, and
chicken farms. Because the threats to black mudalia are of a high
magnitude and are imminent, we assigned a listing priority of 2 to this
species.
Rough hornsnail (Pleurocera foremani)--The following summary is
based on information in our files. The rough hornsnail is an aquatic
snail endemic to the Coosa River system in Alabama. It currently is
known to occur at two locations: The lower Yellowleaf Creek in Shelby
County, and the lower Coosa River below Wetumpka Shoals in Elmore
County. Searches of historical habitats in the Coosa River and its
tributaries have failed to locate the species at other localities. The
two surviving populations are extremely small and localized. The
historical habitats of the rough hornsnail have been extensively
modified by six large dams constructed for hydropower production. Dams
eliminate or reduce currents within impounded areas, allowing sediments
to accumulate on inundated channel habitats. Impounded waters also
experience changes in water chemistry that can affect survival or
reproduction of pleurocerid snails. Currently, the primary threat to
the rough hornsnail is habitat destruction and modification related to
poor water quality and habitat deterioration that result from point
source discharges and/or surface runoff. These actions cause
nutrification, decreased dissolved oxygen concentration, increased
acidity and conductivity, and other changes in water chemistry that can
seriously affect aquatic snails. Both populations of the rough
hornsnail are in areas currently experiencing high human population
growth and development. Because the threats are ongoing and are of a
high magnitude, we assigned the rough hornsnail a listing priority of
2.
Insects
Florida leafwing butterfly (Anaea troglodyta floridalis)--The
Florida leafwing is endemic to south Florida and the Keys; it occurs
only within pine rocklands that retain its sole hostplant, pineland
croton (Croton linearis). Once locally common within the formerly
widespread pine rockland habitat that occurred within Miami-Dade and
Monroe Counties and less common and sporadic within Collier, Martin,
Palm Beach, and Broward Counties, the leafwing now has small and
isolated populations at only two locations: On Big Pine Key in the
lower Florida Keys, and Long Pine Key on the Florida mainland. On Big
Pine Key, the butterfly and its habitat occur on National Key Deer
Refuge (NKDR) and also on other scattered private and public lands
within the vicinity of NKDR. On the Florida mainland, the population on
Long Pine Key is within Everglades National Park (ENP). Pine rockland
fragments on the mainland near or adjacent to ENP may still retain the
potential to support some small, localized, and sporadic populations of
the butterfly, but no Florida leafwings have been documented as
occurring in such areas outside ENP for the last several years.
Land developments of various types have greatly reduced pinelands
in Florida. Within the Keys, pinelands containing the pineland croton
hostplant now occur only on Big Pine Key, with an estimated 80 hectares
(ha) (198 acres) within NKDR and small, scattered relict sites
elsewhere. On the mainland, an estimated 1,068 ha (2,638 acres) of
appropriate hostplant-bearing habitat occur within ENP on Long Pine
Key; outside that area, in Miami-Dade County, scattered fragments of
pine rockland containing pineland croton occur in fragments that
collectively total approximately 370 (ha) (916 acres), roughly half of
which are in private ownership. Collectively, the Big Pine Key, Long
Pine Key, and relict pine rocklands adjacent to ENP presently support
an estimated total of 100-800 adult Florida leafwing butterflies at any
given time.
The Florida leafwing is vulnerable to impacts that probably did not
pose significant risks to its continued existence in the past, when
suitable habitat and the species were much more abundant and
widespread. Habitat destruction and modification is a continuing
problem on public and private lands. This includes habitat loss due to
unnatural or altered fire regimes. Natural fires are important in
maintaining the herbaceous layer of
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pine rocklands, of which the butterfly's sole hostplant, pineland
croton, is a part. Without these fires, succession from pinelands to
hardwood hammocks is rapid, with loss of suitable habitat for the
Florida leafwing. Due to the proximity of remaining pine rockland
habitat to urban areas in southern Florida and the Keys, most natural
fires have been and are suppressed, often replaced by inconsistent
regimes of managed or prescribed fires that do not necessarily result
in habitat conditions suitable for the Florida leafwing. Prescribed
burning occurs on portions of ENP on Long Pine Key, and ENP is working
on incorporating considerations for life histories of select butterfly
species into their management. At NKDR, private homes and light
commercial uses are embedded within or in close proximity to the fire-
sustained pineland habitat. Thus management of pine rocklands is
particularly difficult due to the mixed pattern of land ownership and
development. Fire suppression to protect residential areas results in
the invasion and replacement of native pine rockland habitat by
hardwood hammocks, thereby causing continued loss of habitat for the
leafwing. Survey data collected from mid-2003 through July 2006
indicate a substantial decline in leafwing numbers on NKDR, even within
an area where prescribed burning occurs. Outside of NKDR and ENP, much
of the remaining suitable habitat for the Florida leafwing on private
land is subject to destruction or modification due to the effects of
fire suppression or due to the nature of prescribed fire activities,
and continued economic development that results in conversion of pine
rocklands to other uses.
The continued existence of the Florida leafwing also is threatened
due to other natural and human-related factors. Pesticides used in
mosquito control practices are a major threat on Big Pine Key, where
nearly all occupied and suitable habitat for the Florida leafwing is
exposed to mosquito control chemicals. Studies have shown that the
pesticides used for mosquito control at field application rates are
extremely toxic to non-target butterflies, skippers, and moths.
Essentially all of the pine rocklands within NKDR except one area,
Watson's Hammock, are sprayed and residential areas and roadsides
across Big Pine Key are treated. Also, chemical drift of pesticides has
been found 750 meters (2,460 feet) within the borders of the no-spray
zone on Watson's Hammock. Mosquito control poses much less of a risk to
the leafwings in ENP, as mosquito control on Long Pine Key is limited
to residential areas and campgrounds. Additional natural and human-
related factors include the risk of direct mortality and habitat loss
due to extreme weather events (e.g. hurricanes, tropical storms), and
risk of reduced genetic diversity; both of these risks are heightened
due to the reduction of the Florida leafwing to small, isolated
populations.
The established interest in specimens of the leafwing and
information requests regarding its location from collectors,
researchers, and others suggests that collection may be occurring and
has the potential to occur at any time. However, we do not have
sufficient information to conclude that overutilization for commercial,
recreational, scientific, or educational purposes is a factor that
threatens the Florida leafwing. The principal threats to the Florida
leafwing at this time are the destruction, modification, or curtailment
of its habitat or range, and other natural or manmade factors affecting
its continued existence. Based threats of high magnitude that are
imminent, we assigned a listing priority number of 3 to the Florida
eafwing butterfly.
Bartram's hairstreak butterfly (Strymon acis bartrami)--The
following summary is based on information in our files. The Bartram's
hairstreak is a subspecies endemic to south Florida and the Keys. Like
the Florida leafwing butterfly (described above) it occurs only within
pine rocklands that retain its sole hostplant, pineland croton (Croton
linearis). Once locally common within the formerly widespread pine
rockland habitat that occurred within Miami-Dade and Monroe Counties,
and less common and sporadic within Collier, Palm Beach, and Broward
Counties, the Bartram's hairstreak is now largely restricted to two
locations: Big Pine Key in the Florida Keys, and Long Pine Key on the
Florida mainland. On Big Pine Key, the butterfly and its habitat occur
on National Key Deer Refuge and also on other scattered private and
public lands in the vicinity of NKDR. On Long Pine Key the species is
within Everglades National Park. Pine rockland fragments near or
adjacent to ENP also appear to retain some small, localized, and
sporadic populations of the butterfly. The same factors identified as
threats to the Florida leafwing butterfly (summarized above) also
threaten Bartram's hairstreak. Based on threats of high magnitude that
are imminent, we assigned a listing priority number of 3 to Bartram's
hairstreak butterfly.
Flowering Plants
Harrisia aboriginum (Aboriginal pricklyapple)--The following
summary is based on information in our files. This cylindrical-stemmed
cactus currently occurs in coastal strand vegetation and tropical
coastal hammocks on coastal islands of Sarasota, Charlotte, and Lee
Counties, Florida, from Longboat Key south to Buck Key in the J.N.
``Ding'' Darling National Wildlife Refuge. Populations are likely to be
on shell mounds or sites with shelly substrates; plants may be quite
close to the mangrove zone, but not in it. This plant always had a
restricted distribution and is now vulnerable to extinction because
only 10 populations are remaining. Each population occurs just above
sea level along the coast, and is threatened by the rise in sea level
that has occurred during the past century and is continuing. Each
population is also threatened by nonnative plant invasions and, in at
least one case, predation by introduced iguanas. Some populations are
on private lands, and these are all vulnerable to habitat destruction
and/or improper management. Additionally, the proximity to the coast,
combined with the very small number of plants in each population, makes
the species vulnerable to hurricanes which have the potential to
overwash islands and extirpate populations. For these reasons, the
magnitude of threats is high. Overall, threats are nonimminent because
public land managers have been and are continuing to address exotic
invasive plant issues. Therefore, we assigned this species a listing
priority number of 5.
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 one case, reflects 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.
Birds
Friendly ground-dove, American Samoa DPS (Gallicolumba stairi
stairi)--The following summary is based on information contained in our
files. The genus Gallicolumba is distributed throughout the Pacific and
Southeast Asia. The genus is represented in the
[[Page 53761]]
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). Threats to this subspecies
have not changed over the past year. Of the primary threats to the
subspecies (predation by nonnative species, poaching, and habitat
loss), predation by nonnative species is thought to be occurring now,
and predation likely has been occurring for several decades. This
predation may be an important impediment to increasing the population.
Predation by introduced species has played a significant role in
reducing, limiting, and extirpating populations of island birds,
especially ground-nesters, in the Pacific and other locations
worldwide. Nonnative predators known or thought to occur in the range
of the friendly ground-dove in American Samoa are feral cats (Felis
catus), Polynesian rats (Rattus exulans), black rats (R. rattus), and
Norway rats (R. norvegicus).
In February of 2005, a hurricane destroyed the habitat of G. stairi
in an area on Olosega Island where the species had been most frequently
recorded. Although this species has coexisted with severe storms for
millennia, this example illustrates the potential for natural
disturbance to exacerbate the effect of anthropogenic disturbance on
small populations. Consistent monitoring using a variety of methods
over the last 5 years yielded few observations 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 forested slopes with an open
understory and a substrate of fine scree or exposed earth; this habitat
is not common in American Samoa. We revised the listing priority number
from a 3 to a 6 to better reflect the fact that the threats posed to
the friendly ground-dove (its small population size and nonnative
predators) are nonimminent but still may occur throughout its range.
Streaked horned lark (Eremophila alpestris strigata)--The following
information is based on information contained in our files. No new
information was provided in the petition received December 11, 2002.
The streaked horned lark occurs in British Columbia (Canada),
Washington State, and Oregon. The streaked horned lark nests on the
ground in sparsely vegetated sites in short-grass dominated habitats,
such as native prairies, coastal dunes, fallow agricultural fields,
lightly to moderately grazed pastures, seasonal mudflats, airports, and
dredged-material formed islands in the Columbia River. It is
essentially extirpated from Canada. In Washington State, surveys show
that there are approximately 380 remaining breeding birds (Pearson and
Altman 2005). In Oregon, the breeding population is estimated to be
approximately 400 birds.
The streaked horned lark's breeding habitat is threatened by loss
and degradation due to conversion of native grasslands to other uses
(such as agriculture, homes, recreational areas, and industry),
encroachment of woody vegetation, and invasion of nonnative plant
species (e.g., Scot's broom and sod-forming grasses). Native prairies
have been nearly eliminated throughout the range of the species. It is
estimated that less than 1 to 3 percent of the native grassland and
savanna remains. Those that remain have been invaded by nonnative sod-
forming grasses. Coastal nesting areas have suffered the same fate.
Wintering habitats are seemingly few, and susceptible to unpredictable
conversion to unsuitable overwintering habitat. Where larks inhabit
nonnative habitats similar in structure to native prairies (such as
airports, military reservations, agricultural fields, and dredge formed
islands), they are subjected to a variety of unintentional human
disturbances such as mowing, recreational and military activities,
plowing, flooding, and dredge spoil dumping during the nesting season,
as well as intentional disturbances such as at the McChord AFB where
falcons and dogs are used to haze the birds in order to avoid aircraft
collisions. In some areas, landowners have taken steps to improve
streaked horned lark nesting habitat.
The magnitude of threat is high due to small populations with low
genetic diversity and patchy and isolated habitats in areas desirable
for development. The threat of invasive plant species is high and
constant. The numbers of individuals are low and the numbers of
populations are few. Overwintering birds are concentrated in larger
flocks and subject to unpredictable wintering habitat loss, potentially
affecting a large portion of the population at one time. In Washington,
known populations occur on airports and two military bases where
management and training activities can negatively affect streaked
horned lark breeding. In British Columbia, the one potentially
remaining site with breeding birds occurs at an airport. The immediacy
of threat is imminent, due to the continued loss of suitable lark
habitat, risks to the wintering populations, plans for development on
and adjacent to two of its nesting areas, use of falcons and dogs to
haze breeding birds at McChord AFB, planned expansions of the McChord
AFB west ramp and Olympia airport, the planned addition of 130 more
helicopters at the Gray Army Airfield, and annual Air Force military
training and fire bombing on top of lark nesting habitat. Because of
the increased imminence of threats, we changed the listing priority
number for the streaked horned lark from 6 to 3.
Reptiles
Black pine snake (Pituophis melanoleucus lodingi)-- There are
historical records for the black pine snake from one parish in
Louisiana, 14 counties in Mississippi, and 3 counties in Alabama west
of the Mobile River Delta. Black pine snake surveys and trapping
indicate that this species has been extirpated from Louisiana and from
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 on the DeSoto National Forest. Populations occurring on
properties managed by city and State agencies as gopher tortoise
mitigation banks or wildlife management areas represent the best
opportunities for long-term survival of the species in Alabama. 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 the imminent threat of high
magnitude caused by the past destruction of most of the longleaf pine
habitat of the black pine snake, and the continuing persistent
degradation of what remains, we assigned a listing priority number of 3
to this subspecies. Although there is no actual change in threats over
the past year, habitat loss represents an ongoing or imminent threat to
the black pine snake. Therefore, to help ensure consistency in
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the application of our listing priority process, we changed the listing
priority number from a 6 to a 3 to reflect that the threats are
imminent.
Louisiana pine snake (Pituophis ruthveni)--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
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 affect Louisiana pine
snake population and community structure.
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. The pro-active partnerships to
address key management concerns and research needs are growing and
these conservation efforts have reduced the magnitude of the threats
from high to moderate. However, the primary threat from habitat loss
continues and is, therefore, imminent. Thus, based on threats of
moderate to low magnitude that are imminent, we have changed the
listing priority number from a 5 to an 8.
Amphibians
Relict leopard frog (Rana onca)--This leopard frog was considered
extinct since the 1950s, until it was rediscovered in two relatively
small areas in southern Nevada and a spring in extreme northwestern
Arizona. We estimate that the current distribution of the species is 10
to 20 percent of its historical distribution. Habitat conversion to
agriculture, water diversions, habitat fragmentation such as
construction of Hoover Dam and creation of Lake Mead and Lake Mojave,
and introduction and establishment of nonnative predators and
competitors are believed to be the primary causes of historical
population declines and reduction in the range and distribution of the
frog. Currently, the primary threats are low numbers of individuals and
populations, nonnative predators and competitors, and the potential for
water diversion or ground water pumping. A conservation agreement and
strategy completed in 2005 will serve as the management plan for the
species. As prescribed in the agreement and strategy, annual work plans
will be developed and implemented to monitor threats and the status of
the species as well as accomplish conservation actions for the species.
The magnitude of existing threats is moderate, which we lowered from
the previous determination of high magnitude in 2005. This change in
magnitude is largely based on successful captive-rearing and
translocation efforts. These threats remain nonimminent since there are
no known projects or actions that would adversely affect frog
populations or threaten surface water associated with known sites
occupied by the frog. Thus, we changed the listing priority number from
a 5 to an 11 for this species.
Fishes
Cumberland darter (Etheostoma susanae)--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 fish species is
an approximately 3-inch member of the family Percidae that is endemic
to the upper Cumberland River system (above Cumberland Falls) in
Kentucky and Tennessee. Currently, the species is restricted to 16
headwater streams in Kentucky and 2 streams in Tennessee. Within these
streams, the Cumberland darter inhabits low-velocity, shallow riffles
and backwater areas of moderate-to low-gradient stream reaches with
stable sand or sandy-gravel substrates. The primary threat to the
species is siltation of instream habitats caused by coal mining
activities, silvicultural practices, road construction, and urban
development. Because the species is limited to only 18 known
populations, the magnitude of threat for the species is high; these
populations are isolated from one another by poor-quality habitat,
impoundments, or natural barriers. The immediacy of threat is
nonimminent because (1) Federal and State water quality laws have
reduced water quality and habitat threats to some degree, (2) non-point
pollution threats and modification of reach geomorphology and hydrology
are cumulative and gradual, and (3) approximately 40 percent of
watersheds supporting the species are provided habitat and water
quality protection through Federal ownership (Daniel Boone National
Forest). Consequently, we assigned a listing priority number of 5 to
this species. This represents a change in the previous listing priority
number, from 6 to 5, due to a change in taxonomic status for the
species, not because of a change in threat magnitude or imminence. The
Cumberland Johnny darter, E. nigrum susanae, was elevated to specific
status (E. susanae, Cumberland darter) based on new molecular evidence
showing that this subspecies has distinct mitochondrial DNA haplotypes
not found in the Johnny darter, E. nigrum nigrum.
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. This species is endemic to
upland portions of the Black Warrior River system in Alabama where it
occurs in shallow headwater streams. This species is uncommon and
sporadic within its range, as it favors shallow, flowing water in
spring runs and spring-associated streams with emergent vegetation.
Only three disjunct populations are known: One in the Clear Creek
system in Winston County, one in spring-fed tributaries of Turkey Creek
in Jefferson County; and one population in Little Cove Creek (Cove
Springs) in Etowah County.
The Jefferson County population (Turkey Creek), which is located in
a large metropolitan area, is threatened by urbanization and
commercialization of its habitat. Siltation from bridge, road, and
sewer line construction has been recently documented within the Turkey
Creek watershed by academic researchers and Service biologists. The
major threat to the Winston County population of rush darters is
erosion in Mill Creek, Doe Branch, and Wildcat Branch, and the
cumulative increase of
[[Page 53763]]
sediments caused from gravel roads and roadside ditches. Within the
past year, biologists have observed increased erosion along roads
adjacent to Doe and Wildcat Branches which resulted in increased
siltation within those streams. Increased urbanization, road
maintenance and silviculture practices contribute to increased
sedimentation in the watershed. The major threat to the Cove Springs
population is contamination of the water with chlorine. Efforts are
underway to improve habitat and water quality; however, at this time
all populations are being negatively affected by declining water
quality. The magnitude of threat is high due to the limited number of
populations. We changed the listing priority from a 5 to a 2 based on
the imminent threat; the threat is imminent because water quality is
currently declining for all populations.
Clams
Altamaha spinymussel (Elliptio spinosa)--The following summary is
based on information in our files. The Altamaha spinymussel is a
freshwater mussel endemic to the Altamaha River drainage of
southeastern Georgia. The historical range 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 species is associated with stable, coarse to fine sandy sediments
of sandbars and sloughs and appears to be restricted to swiftly flowing
water. The species appears to be extirpated from the Ohoopee and Oconee
Rivers, and its numbers are greatly reduced in the Ocmulgee and
Altamaha Rivers. Altamaha spinymussels face severe habitat degradation
from a number of sources. Primary among these are threats from
sedimentation and contaminants within the rivers that the Altamaha
spinymussel inhabits. A new threat of deadhead logging has recently
emerged. These threats to the Altamaha spinymussel are further
compounded by its limited distribution and the low population size
identified in recent survey efforts. Efforts to identify the host fish
and expand our understanding of the spinymussels' life cycle have not
produced results, attempts to investigate potential impacts caused by
heavy metals have not received funding, a survey conducted in 2004 in
the Ocmulgee found no spinymussels, and deadhead logging presents an
added threat. Consequently, we now consider the threats to be imminent
and have changed the listing priority number from a 5 to a 2 for this
species.
Insects
Wekiu bug (Nysius wekiuicola)--The wekiu bug belongs to the true
bug family, Lygaeidae, and is endemic to the island of Hawaii. This
species only occurs on the summit of Mauna Kea and feeds upon other
insect species which are blown to the summit of this large volcano. The
wekiu bug is primarily threatened by the loss of its habitat from
astronomy development. In 2004 and early 2005, surveys were conducted
that found multiple new locations of the wekiu bug on Mauna Kea summit.
Several of these cinder cones within the Mauna Kea Science Reserve, as
well as two other cinder cones located in the State Ice Age Natural
Area Reserve, are not currently undergoing development nor is
development planned. With the discovery of these new locations, the
threats, though ongoing, do not occur across the entire range of the
wekiu bug. The immediacy of the threats is imminent in some part of the
weiku bug's range because ongoing development is occurring in the Keck
Observatory Outrigger telescope project area. This development will
establish six new interferometry telescopes around the existing Keck
facility. A mitigation plan is in place that will require a 3:1
replacement of damaged habitat. However, the effectiveness of this
mitigation is untested and unknown. Although the threats are ongoing in
some areas of wekiu bug habitat, the recent discoveries of new
locations of the wekiu bug in areas that are not subject to the primary
threat of astronomy development reduces the magnitude of the threat
from high to moderate. Therefore, we are changing the listing priority
number for this species from a 2 to an 8.
Crustaceans
Anchialine pool shrimp (Vetericaris chaceorum)--Vetericaris
chaceorum is an anchialine pool-inhabiting species of shrimp belonging
to the family, Procarididae; it is the only species in its genus. This
species is endemic to the Hawaiian Islands and is only known from one
population in a single pool on the island of Hawaii. There are two
primary threats to this species. First, fish do not naturally occur in
the pool inhabited by the species, and it would be highly vulnerable to
predation by any intentionally or accidentally introduced fish.
Anchialine pools have been used to discard or hold bait-fish and/or
aquarium fish. Second, the species is vulnerable to habitat loss due to
degradation by dumping or fill, or recreational activities. This
activity has occurred in the past but this pool now lies within lands
administered by the State of Hawaii Department of Hawaiian Home Lands.
There are no conservation efforts underway to eliminate the potential
for any of these threats. The magnitude of threats remains high because
of the devastating effect that realization of these threats could have
on the species because of its restriction to a single pool. However, we
changed the listing priority number for this species from a 1 to a 4
because the threats are nonimminent: Fish have not been introduced into
the pool (nor is there any reason to believe that introduction is
imminent) and a site visit in early 2005 showed there were no signs of
dumping or fill.
Anchialine pool shrimp (Metabetaeus lohena)--Metabetaeus lohena is
an anchialine pool inhabiting species of shrimp belonging to the family
Alpheidae. This species is endemic to the Hawaiian Islands and is
currently known from populations on the islands of Oahu, Maui, and
Hawaii. The primary threats to this species are predation by fish
(which do not naturally occur in the pools inhabited by this species)
and habitat loss from degradation. The pools where this species occurs
on Maui and Hawaii are located within State Natural Area Reserves
(NAR). Hawaii's State statutes prohibit the collection of the species
and the disturbance of the pools in State NARs. However, enforcement of
these prohibitions is difficult and the negative effects from the
introduction of fish are extensive and happen quickly. Therefore,
threats to this species are of a high magnitude. However, we now
consider the threat of predation from fish to be nonimminent because no
fish were observed during the surveys conducted in the NARs for this
shrimp in 2004 and no recent habitat degradation has occurred. In
addition, no nonnative fish were observed during several site visits to
the Oahu location in 2005. Therefore, we changed the listing priority
number of this species from a 2 to a 5.
Anchialine pool shrimp (Palaemonella burnsi)--Palaemonella burnsi
is an anchialine pool inhabiting species of shrimp belonging to the
family, Palaemonidae. This species is endemic to the Hawaiian Islands
and is currently known from three populations on the island of Maui and
one population on the island of Hawaii. The primary threats to this
species are predation by fish (which do not naturally occur in the
pools inhabited by this species) and habitat loss due to degradation.
The pools where this species occurs on Maui are located within a State
Natural Area Reserve
[[Page 53764]]
(NAR). Hawaii's State statutes prohibit the collection of the species
and the disturbance of the pools in State NARs. On the island of
Hawaii, the species occurs within a National Park and collection and
disturbance are also prohibited. However, enforcement of these
prohibitions is difficult, and the negative effects from the
introduction of fish are extensive and happen quickly. Therefore,
threats to this species are of high magnitude. However, we no longer
consider the threats to be imminent, because during a 2004 survey no
fish were observed in the pools where these shrimp occur on Maui or the
island of Hawaii and there was no evidence of recent habitat
degradation. Therefore, the threats of predation from fish and habitat
degradation are nonimminent, and consequently we changed the listing
priority number of this species from a 2 to a 5.
Anchialine pool shrimp (Procaris hawaiana)--Procaris hawaiana is an
anchialine pool inhabiting species of shrimp belonging to the family,
Procarididae. This species is endemic to the Hawaiian Islands and is
currently known from two populations on the island of Maui and one
population on the island of Hawaii. The primary threats to this species
are predation from fish (which do not naturally occur in the pools
inhabited by this species) and habitat loss due to degradation. The
pools where this species occurs on Maui are located within a State
Natural Area Reserve (NAR). Hawaii's State statutes prohibit the
collection of the species and the disturbance of the pools in State
NARs. However, enforcement of these prohibitions is difficult and the
negative effects from the introduction of fish are extensive and happen
quickly. There are no conservation efforts underway to alleviate the
potential for any of these threats in the one pool on the island of
Hawaii. Therefore, threats to this species remain at high magnitude.
However, we no longer consider the threats to be imminent because,
during a 2004 survey, no fish were observed in the pools where these
shrimp occur on Maui or the island of Hawaii. In addition, there were
no signs of dumping or fill on a site visit to the location on the
island of Hawaii in early 2005. Therefore, we changed the listing
priority number of this species from a 2 to a 5.
Flowering plants
Abronia alpina (Ramshaw Meadows sand-verbena)--Abronia alpina is a
small perennial herb, 2.5 to 15.2 centimeters (1 to 6 inches) across
forming compact mats with lavender-pink, trumpet-shaped, and generally
fragment flowers. Abronia alpina is known from one main population
center in Ramshaw Meadow on the Kern Plateau of the Sierra Nevada,
California and from one subpopulation found in adjacent Templeton
Meadow. The total estimated area occupied is approximately 6 hectares
(15 acres). Population estimates from 1985-1994 range from a low of
69,652 plants in 1986 to 132,215 plants in 1987. Surveys conducted
since 1994 indicate that no significant changes have occurred in
population size or location, although, the 2003 survey showed
population numbers to be at the low end of the range. The population
fluctuates from year to year without any clear trends.
The major threats facing A. alpina include habitat disturbance and
trampling from incidental livestock trailing, pack animals, and hikers;
campsite development; and erosion associated with such disturbances. An
additional threat is encroachment of lodgepole pine into areas occupied
by the species. Lodgepole pine encroachment has altered the meadow and
becoming established within A. alpina habitat. Lodgepole pine
encroachment may alter soil characteristics by increasing organic
matter levels, decreasing porosity, and moderating diurnal temperature
fluctuations thus reducing the competitive ability of A. alpina to
persist in an environment more hospitable to other plant species. The
Ramshaw Meadow ecosystem is subject to alteration by lowering of the
water table due to downcutting of the South Fork of the Kern River
(SFKR). The SFKR flows through Ramshaw Meadow, at times coming within
15 meters (50 feet) of A. alpina habitat, particularly in the vicinity
of five subpopulations. The habitat occupied by A. alpina directly
borders the meadow sy