Endangered and Threatened Wildlife and Plants; 12-Month Finding on a Petition To Delist the Idaho Springsnail; 12-Month Finding on a Petition To List the Jackson Lake Springsnail, Harney Lake Springsnail, and Columbia Springsnail; and Proposed Rule To Remove the Idaho Springsnail From the List of Threatened and Endangered Wildlife, 56938-56948 [E6-15915]
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in the northeastern United States
(Halonen 2000, p. 15).
The information presented in the
petition suggests that Usnea longissima
populations are facing increased
pressure in California from several
factors, including habitat loss and
commercial timber harvesting. In the
Coast Range of the Pacific Northwest, U.
longissima seems more limited in
occurrences by its inability to easily
disperse than by the possible lack of
suitable habitat (Keon 2001, p. 92–94).
U. longissima disperses mostly from
small pieces fragmenting from the main
plant and being carried off in the wind,
by an animal, or by simply falling onto
another plant (Pojar and Makinnon
1994, p. 503). This lichen has a short
dispersal distance, usually less than 5
meters (16 feet) (McCune and Geiser
1997, pp. 301, 307, and 353). Therefore,
U. longissima recolonization of second
growth forests may be more dependent
upon proximity to existing U.
longissima populations than on other
habitat characteristics, such as tree age
(Keon and Muir 2002, pp. 233–242).
Review of the Petition
The petition states that Usnea
longissima has been extirpated from
much of its former range in western
Europe primarily due to intensive evenaged logging and acid rain, and that it
is being extirpated in California through
habitat disturbance. The petition
contends that U. longissima is highly
dependent on large, mature trees for
habitat and that logging of old-growth
forest is leading to its extirpation. Our
review of the information present in the
petition suggests that air quality has also
contributed to the extirpation of the
Usnea longissima in some parts of
Europe. The petition requests that the
California populations of U. longissima
be listed under the Act as endangered or
threatened.
However, the petition contains no
information about whether western
Europe or California is a significant
portion of the species’ range. Therefore,
the petition does not provide substantial
information that areas in western
Europe or California constitute a
significant portion of the species’ global
range. The petition also does not request
that we list the species across its range.
To list the species in California alone,
as requested by the petitioner, we would
have to determine that the occurrences
in California constitute a Distinct
Population Segment. The Act restricts
the use of Distinct Population Segments
to vertebrate animal species (16 U.S.C.
1532(16); 61 FR 4722; February 7, 1996).
U. longissima is not a vertebrate animal,
and thus we have no authority to list a
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distinct population segment of this
species. Therefore, the California
populations of U. longissima are not
considered to be a listable entity
pursuant to the Act and as a result are
ineligible for listing.
Regarding the petitioner’s contention
that U. longissima is dependent on large
mature trees, we note that studies
addressing Usnea longissima
distributions in coastal Oregon forests
(Keon 2001, pp. 92–94; Keon and Muir
2002, pp. 233–242) and reviews of U.
longissima occurrences on Pacific
Lumber Company (PALCO) lands in
northern coastal California (Leppig
2003, pp. 1–3) suggest that U.
longissima occurrences may be more
dependent on the species’ ability to
disperse than on the age of the host
trees. Leppig’s review (2003, p. 2) of U.
longissima on PALCO lands determined
that it occurs on all tree species present
in the stands and is relatively abundant
in younger, 20- to 30-year-old forest
stands. Keon and Muir (2002, pp. 233–
242) found that U. longissima
transplants in young stands grew
hardier than transplants in an old
growth setting. Additionally, our
reviews of PALCO timber harvest plans
suggest that U. longissima is relatively
abundant in watersheds that have been
previously harvested (Leppig 2003, p.
2), suggesting that U. longissima
populations are resilient. In summary,
although Pojar and Makinnon (1994, p.
503) found that the healthiest
populations of U. longissima are in oldgrowth forests, this slow-growing lichen
is not restricted to such an age class. In
addition, contrary to the implications in
the petition, where the species has been
studied in the Pacific Northwest, it
occurs with relative abundance in
younger 20- to 30-year-old forest stands
(Leppig 2003, pp. 1–3) and in
watersheds that have undergone forest
harvests (Leppig 2003, p. 2).
Finding
We reviewed the petition to list Usnea
longissima in California and the
literature cited in the petition, and we
evaluated that information in relation to
other pertinent literature and
information available to us. After this
review and evaluation, we find that
there is not substantial scientific or
commercial information to demonstrate
that the California populations of U.
longissima are a listable entity, and as
a result, we have determined that the
petitioned action is not warranted.
Although we will not be commencing a
status review in response to this
petition, we encourage interested parties
to continue to gather data that will assist
with the conservation of the species.
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References Cited
A complete list of all references cited
herein is available upon request from
the Arcata Fish and Wildlife Office (see
ADDRESSES).
Author
The primary authors of this notice are
the staff of the Arcata Fish and Wildlife
Office (see ADDRESSES).
Authority: The authority for this action is
the Endangered Species Act of 1973, as
amended (16 U.S.C. 1531 et seq.).
Dated: September 20, 2006.
Marshall P. Jones, Jr.,
Acting Director, Fish and Wildlife Service.
[FR Doc. E6–15876 Filed 9–27–06; 8:45 am]
BILLING CODE 4310–55–P
DEPARTMENT OF THE INTERIOR
Fish and Wildlife Service
50 CFR Part 17
RIN 1018–AU66
Endangered and Threatened Wildlife
and Plants; 12-Month Finding on a
Petition To Delist the Idaho
Springsnail; 12-Month Finding on a
Petition To List the Jackson Lake
Springsnail, Harney Lake Springsnail,
and Columbia Springsnail; and
Proposed Rule To Remove the Idaho
Springsnail From the List of
Threatened and Endangered Wildlife
Fish and Wildlife Service,
Interior.
ACTION: Notice of two 12-month petition
findings and a proposed rule to delist
the Idaho springsnail (Pyrgulopsis
idahoensis).
AGENCY:
SUMMARY: We, the U.S. Fish and
Wildlife Service (USFWS, Service, or
we), under the Endangered Species Act
of 1973, as amended (Act), announce
combined 12-month findings on a
petition to delist the endangered Idaho
springsnail (Pyrgulopsis idahoensis) and
a petition to list the Jackson Lake
springsnail (P. robusta), Harney Lake
springsnail (P. hendersoni), and
Columbia springsnail (P. species A
(unnamed)). Evidence collected
subsequent to the December 14, 1992,
listing (USFWS 1992, pp. 59244–59527
(57 FR 59244)) of the Idaho springsnail
indicates it no longer constitutes a
distinct species. It is now described as
the Jackson Lake springsnail (P.
robusta), a single taxon, composed of
four previously distinct springsnail
species (Idaho, Jackson Lake, Harney
Lake, and Columbia springsnails), and
therefore we are proposing to remove
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the Idaho springsnail from the Federal
List of Endangered and Threatened
Wildlife. We evaluated the best
available scientific and commercial
information regarding the status of, and
threats to, the newly described P.
robusta, and determined that the threats
to the species do not warrant its listing
at this time. Additionally, based on our
status review of P. robusta, we also find
that listing the Jackson Lake springsnail,
Harney Lake springsnail, and Columbia
springsnail as separate species is not
warranted.
The 12-month findings on the
delisting and listing petitions
announced in this notice were made on
September 28, 2006. We request that
new information be submitted to us
concerning the status of, or threats to,
Pyrgulopsis robusta, whenever it
becomes available.
We will accept comments from all
interested parties regarding the proposal
to delist the Idaho springsnail until
November 27, 2006. We must receive
requests for public hearings on or before
November 13, 2006.
ADDRESSES: Comments may be
submitted on the proposed rule to delist
the Idaho springsnail by any of the
following methods. Please include RIN
1018–AU66 in any subject line.
• E-mail:
fws1srbocomments@fws.gov.
• Fax: (208) 378–5262.
• Hand carry, Postal Delivery, or
Courier: Snake River Fish and Wildlife
Office, U.S. Fish and Wildlife Service,
1387 S. Vinnell Way, Room 368, Boise,
ID 83709.
• Federal Rulemaking Portal: https://
www.regulations.gov. Follow the
instructions for submitting comments.
Please see the Public Comments
Solicited section below for file format
and other information about electronic
filing.
DATES:
The
Snake River Fish and Wildlife Office by
mail at the above address; by telephone
at 208/378–5243; by facsimile at 208/
378–5262; or by electronic mail at:
fw1srbocomment@fws.gov.
FOR FURTHER INFORMATION CONTACT:
SUPPLEMENTARY INFORMATION:
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Public Comments Solicited
We intend that any final action
resulting from this proposal will be as
accurate and effective as possible.
Therefore, comments or suggestions
from the public, other concerned
governmental agencies, Native
American Tribes, the scientific
community, industry, or any other
interested party concerning this
proposed rule are hereby solicited.
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Please note that comments merely
stating support or opposition to the
actions under consideration without
providing supporting information,
although noted, will not be considered
in making a determination, because
section 4(b)(1)(A) of the Act directs that
determinations as to whether any
species is a threatened or endangered
species shall be made ‘‘solely on the
basis of the best scientific and
commercial data available.’’
You may submit materials concerning
this proposal by any one of several
methods (see ADDRESSES section). Please
submit Internet comments to
fws1srbocomments@fws.gov in ASCII
file format and avoid the use of special
characters or any form of encryption.
Please also include ‘‘RIN 1018–AU66’’
in your e-mail subject header and your
name and return address in the body of
your message. If you do not receive a
confirmation from the system that we
have received your Internet message,
contact us directly (see ADDRESSES).
Please note that the Internet address
fws1srbocomments@fws.gov will be
unavailable at the termination of the
public comment period.
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
rulemaking 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.
Comments and other information
received, as well as supporting
information used to write this rule, will
be available for public inspection, by
appointment, during normal business
hours at the above address. In making a
final decision on this proposal, we will
take into consideration any additional
information we receive. Such
communications may lead to a final
regulation that differs from this
proposal.
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Background
Section 4(b)(3)(B) of the Endangered
Species Act of 1973, as amended (Act)
(16 U.S.C. 1531 et seq.) requires that, for
any petition to revise the List of
Threatened and Endangered Species
that contains substantial scientific and
commercial information that suggests a
change in status may be warranted, we
make a finding within 12 months of the
date of the receipt of the petition on
whether the petitioned action is: (a) Not
warranted; (b) warranted; or (c)
warranted, but the immediate proposal
of a regulation implementing the
petitioned action is precluded by other
pending proposals to determine whether
a species is threatened or endangered,
and expeditious progress is being made
to add or remove qualified species from
the List of Threatened and Endangered
Species. Such 12-month findings are to
be promptly published in the Federal
Register. In addition, section 4(b)(3)(C)
of the Act requires that a petition for
which the requested action is found to
be warranted but precluded shall be
treated as though resubmitted on the
date of such finding (i.e., requiring a
subsequent finding to be made within
12 months).
Previous Federal Action
We published the final rule listing the
Idaho springsnail as endangered on
December 14, 1992 (57 FR 59244). In
that rule, we described range reduction,
continued adverse habitat modification,
deteriorating water quality from
multiple sources, and the appearance of
the invasive New Zealand mudsnail
(Potamopyrgus antipodarum) as the
major threats to the species. We have
not designated critical habitat for the
Idaho springsnail.
On June 28, 2004, we received a
petition from the Idaho Office of Species
Conservation and the Idaho Power
Company (IPC) requesting that the Idaho
springsnail be delisted based on a recent
taxonomic revision of the species. The
petitioners also provided new Idaho
springsnail scientific information, and
contrasted this new information with
information used in the 1992 Idaho
springsnail listing decision (57 FR
59244). The petitioners stated that most,
if not all, threats to Idaho springsnail
identified in the 1992 listing rule have
been eliminated, are being actively
addressed by State and private entities,
or are not relevant, based on new
scientific information.
On August 5, 2004, we received a
petition from Dr. Peter Bowler, the
Biodiversity Conservation Alliance, the
Center for Biological Diversity, the
Center for Native Ecosystems, the
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Western Watersheds Project, and the
Xerces Society, requesting that the
Jackson Lake springsnail, Harney Lake
springsnail, and Columbia springsnail
be listed as either threatened or
endangered species, and as either
individual species or combined as the
new species, Pyrgulopsis robusta. This
listing petition cited habitat loss and
degradation from development
impacting springs, domestic livestock
grazing, and groundwater withdrawal,
among other factors, as threats to the
continued existence of these three
springsnail species. The listing petition
also discussed the recent springsnail
taxonomic revision and acknowledged
that the Jackson Lake springsnail,
Harney Lake springsnail, Columbia
springsnail, and Idaho springsnail may
be one species (P. robusta), but
contended that, whether considered
individually or as one species, all four
springsnails warranted the protection of
the Act.
On April 20, 2005, we published
combined 90-day petition findings
(USFWS 2005, pp. 20512–20514 (70 FR
20512)), stating that both petitions
provided substantial information
suggesting that delisting of the Idaho
springsnail, or listing of Jackson Lake
springsnail, Harney Lake springsnail,
and Columbia springsnail, may be
warranted.
Species Information
The Idaho springsnail (Pyrgulopsis
idahoensis; Hydrobiidae) was first
described by Pilsbry (1933, pp. 11–12)
and placed in the genus Amnicola. Greg
and Taylor (1965, pp. 103–110)
established the new genus Fontelicella
and then placed P. idahoensis in the
subgenus Natricola, created in 1965
(Greg and Taylor 1965, pp. 108–109).
Natricola contained the Idaho
springsnail, the Harney Lake springsnail
(P. hendersoni), and the Jackson Lake
springsnail (P. robusta). After several
taxonomic revisions, the subgenus
Natricola was placed in synonymy with
the genus Pyrgulopsis by Hershler and
Thompson (1987, p. 29). Pyrgulopsis is
the largest genus of freshwater mollusks
in North America, comprised of over
120 described species (Liu and Hershler
2005, p. 284). The greatest diversity of
the genus occurs in the Great Basin of
the western United States (Hershler and
Sada 2000, p. 367; Hershler and Sada
2002, p. 255).
In 2004, Hershler and Liu (2004, pp.
78–79) revised the taxonomic status of
four springsnails Pyrgulopsis
idahoensis, P. hendersoni, P. robusta,
and the Columbia springsnail (P. species
A (unnamed)), by placing all four
springsnails into the oldest available
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taxon of the four revised species, P.
robusta (Jackson Lake springsnail,
Walker 1908, p. 97). All four species
were considered members of the
subgenus Natricola. Members of the
subgenus Natricola are very similar in
size and shape, being distinguished
primarily by the morphology of the
shell. The authors reviewed
morphological characters,
mitochondrial DNA sequences, and
nuclear DNA sequences to establish the
need for taxonomic status change.
Several morphological metrics,
including the position of the callus
(thickened portion) on the operculum
(serves as a cover for the opening in the
shell); the shape of the central cusp of
the central teeth; the number of cusps
on central teeth; notching of inner
marginal teeth; number of cusps on
outer marginal teeth; the male penile
features; and female genitals, did not
differ significantly among the four
springsnail species (Hershler and Liu
2004, pp. 70–75). Five shell parameters
were significantly heterogeneous in a
comparison of the four springsnail
species. In only one case did a single
springsnail species differ significantly
from the other three; the Idaho
springsnail differed significantly from
the other three springsnail species for
the ratio of shell height to height of
body whorl (Hershler and Liu 2004, p.
71).
To construct species topologies,
Hershler and Liu (2004, pp. 67–69)
sequenced selected genes of four
springsnail species, Pyrgulopsis robusta,
P. idahoensis, P. hendersoni, and P.
species A (unnamed), as well as
congeners P. imperialis, P. intermedia,
P. kolobensis, and P. species B
(unnamed). The mitochondrial DNA
data revealed little difference in the
partial CO1 gene among the four
springsnail species. Differences ranged
from 0.0 to 0.8 percent (0 to 5 base
pairs) among the four springsnail
species and 2.6 to 6.9 percent (16 to 43
base pairs) with congeners. Nuclear
DNA data revealed differences in the
ITS–1 sequences within the four
springsnail species that were
substantially smaller (0.0 to 0.6 percent)
than differences among other congeners
(5.9 to 20.4 percent) (see Figure 8 in
Hershler and Liu 2004, pp. 73–75).
These two lines of evidence show that
DNA sequence differences among the
four springsnail species are very small
compared to differences with other
recognized taxa within the genus
Pyrgulopsis.
Hershler and Liu (2004, p. 77)
concluded ‘‘three independent data sets
(morphology, mitochondrial, and
nuclear DNA sequences) congruently
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suggest that these four Natricola snails
do not merit recognition as distinct
species according to various currently
applied concepts of this taxonomic
rank.’’ The methods employed by
Hershler and Liu (2004, pp. 67–70) are
considered contemporary in the field of
genetics and are consistent with those
used by numerous authors
reconstructing phylogenies based on
molecular evidence in general
(Raahauge and Kristensen 2000, pp. 87–
89; Jones et al. 2001, pp. 281; Attwood
et al. 2003, pp. 265–266), and with
western hydrobiid snails in particular
(Hershler et al. 2003, pp. 358–359; Liu
et al. 2003, pp. 2772–2775; Hurt 2004,
pp. 1174–1177; Liu and Hershler 2005,
p. 285). Further, it is the position of the
American Malacological Society that the
Hershler and Liu (2004) revised
taxonomy sets the standard for
understanding this group of springsnails
(Leal 2004). Hershler and Liu (2004, pp.
66–81) represents the best available
scientific and commercial data on the
taxonomic status of the four petitioned
springsnails, and we therefore will refer
to the four former springsnail species as
Pyrgulopsis robusta for the rest of this
document.
Biology
Pyrgulopsis robusta shells are large
for the genus, usually ovate (oval) to
narrow-conic (cone shaped), rarely
subglobose (not quite rounded), with
whorls weakly to moderately convex
(curving outward). The shell is clearwhite and the periostracum (outer layer
of the shell matrix) is tan. The aperture
is ovate and weakly angled above. The
inner lip is complete in larger
specimens. The penial lobe and filament
are about equal in length. The dorsal
proximal lobule is well developed,
usually overlapping the base of the
filament and often borne on a weak
proximal swelling. The terminal gland
is elongate and transverse. The dorsal
distal lobule is well developed and is
usually bearing one or a series of small
glands. The ventral lobule is well
developed and bears a large gland
(Hershler and Liu 2004, p. 79).
Information available to describe the
life history of Pyrgulopsis robusta varies
widely. The species is hypothesized to
primarily feed on periphyton (i.e.,
diatoms and algae), which covers the
surface of most benthic (submerged
bottom) substrates. Although little
specific information exists regarding
reproductive strategies of P. robusta,
members of the genus Pyrgulopsis are
generally dioecious (i.e., male and
female individuals) (Dillon 2000, pp.
102–103; Lysne 2003, p. 80).
Pyrgulopsis robusta is hypothesized to
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reproduce once in an annual life cycle,
and laboratory studies estimate average
survival to be 382 days (Lysne 2003, p.
82). However, field data show that not
all P. robusta die within a year (Finni
2003a, pp. 3–5), a life history pattern
suggested by Dillon (2000, p. 162) to be
exhibited by many populations,
allowing extended survivorship and
multiple reproductive events.
Additional P. robusta life history
information regarding reproduction and
growth rates can be found in the
following references: Finni 2003a, pp.
3–5; Lysne 2003, pp. 24, 36, 38, 79–81;
Riley et al. 2003, p. 33; Dillon 2000, p.
103; and, Hershler 1994, pp. 1–119.
Habitat
Species in the genus Pyrgulopsis
require permanent fresh waters (Taylor
1985, pp. 265, 276; Hershler 1998, p. 1;
Hershler and Sada 2002, p. 255).
Pyrgulopsis robusta utilizes a wide
range of flow conditions and habitats.
For example, P. robusta has been found
in the mainstem Snake River, Idaho, in
various habitats; in C.J. Strike and Swan
Falls Reservoirs, Idaho (Clark 2005); and
in two springs that flow through
Yellowstone National Park and John D.
Rockefeller National Parkway in
Wyoming: Marmot Spring, a relatively
stable groundwater-fed spring, and
Polecat Creek, a geothermal spring
(Riley 2005a, pp. 1, 8; Hall et al. 2003,
p. 408). In southeastern Oregon, P.
robusta primarily occurs in cold springs
and spring pools of variable size (Frest
and Johannes 1995, p. 196), but is also
found in the South Fork Malheur River
(Hershler and Liu 2004, p. 67). Although
P. robusta evolved in prehistoric Lake
Idaho (Taylor 1982, p. 2; Taylor 1985,
pp. 288, 309), the species presently
occurs more frequently and abundantly
in river habitat than in lake or reservoir
habitat (Clark 2005).
Pyrgulopsis robusta is found on a
wide range of substrates in the Snake
and Columbia Rivers, from silt and
pebbles to cobbles and boulders, but in
the Snake River the species achieves
highest density on gravel to cobble
substrates (Stephenson et al. 2004, A3
pp. 1–4, A4 pp. 1–4). In Southeastern
Oregon, the species is generally found
on coarse sand to cobble substrates but
may also be associated with the
submerged aquatic plant genus Rorippa
(Frest and Johannes 1995, p. 196).
Field and laboratory information
indicate Pyrgulopsis robusta has a wide
temperature tolerance (Stephenson and
Bean 2003, pp. A1, A2; Stephenson et
al. 2004, A3 pp. 1–4, A4 pp. 1–4; Lysne
2003, p. 27). Pyrgulopsis robusta has
been documented to survive and grow at
temperatures that exceeded the State of
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Idaho’s water temperature criteria for
cold-water life of 66 degrees Fahrenheit
(F) (19 degrees Celsius (C)) mean daily
and 72 degrees F (22 degrees C)
maximum daily water temperatures
(Lysne 2003, pp. 27–29). Pyrgulopsis
robusta have been routinely collected in
the Snake River at water temperatures
greater than 68 degrees F (20 degrees C)
(Stephenson and Bean 2003, pp. A1, A2;
Stephenson et al. 2004, A3 pp. 1–4, A4
pp. 1–4). In Wyoming, high numbers of
P. robusta have been collected in
Polecat Creek, a geothermal spring creek
with temperatures ranging from
approximately 57.2 degrees F (14
degrees C) in winter to 75.2 degrees F
(24 degrees C) in summer (Hall et al.
2003, p. 408). Other variables that
potentially influence P. robusta habitat
selection and use have not been well
documented.
Range and Distribution
Pyrgulopsis robusta is now comprised
of four geographically isolated
populations that include the
northwestern Wyoming population, the
Snake River population in Idaho, the
Columbia River population in Oregon
and Washington, and the Oregon closedbasin population (Hershler 1994, p. 91;
Hershler 1998, p. 99; Riley et al. 2003,
p. 6; Frest 2005a; Riley 2005b). In
Wyoming, P. robusta is currently known
from only two locations in Yellowstone
National Park and John D. Rockefeller
National Parkway. There have been past
collections at other sites, and P. robusta
may be found at additional locations in
the future. Recent surveys have failed to
locate the species in Jackson Lake (Riley
2005b), the type locality of P. robusta as
described by Walker in 1908.
In southeastern Oregon, Pyrgulopsis
robusta occurs in few locations (six or
fewer) in the Oregon Interior Basin, in
isolated cold springs and spring pools
(Frest and Johannes 1995, p. 196), and
in the South Fork Malheur River, a
tributary to the Snake River (Hershler
and Liu 2004, p. 67), in Harney and
Lake Counties. Pyrgulopsis robusta was
historically found along the shores of
Malheur and Harney Lakes (Frest and
Johannes 1995, p. 196) and was
associated with open water habitats (as
opposed to wetland habitats with
emergent vegetation) 8,000 to 10,000
years ago (Wriston 2003, p. 28).
Pyrgulopsis robusta is not known to
currently exist in Harney or Malheur
Lakes, and it is uncertain when P.
robusta last existed there (Frest and
Johannes 1995, p. 196). Many isolated
springs and other aquatic habitats of
Utah, Nevada, and Idaho in the Great
Basin, including parts of southeastern
Oregon, have been surveyed specifically
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for springsnails, but no additional P.
robusta have been located (Hershler
1998, p. 3; Hershler and Sada 2002, p.
259).
In the Snake River, Pyrgulopsis
robusta is known to occur at numerous
locations along a stretch of 214 river
miles (344 kilometer (km)) between
river mile (rm) 340 (river kilometer mile
(rkm) 547) and rm 554 (rkm 892). There
have been at least 174 collections from
this reach of river and the extent of P.
robusta is believed to be well defined
and relatively abundant. The
distribution of P. robusta in the
Columbia River is less well known than
in the Snake River, particularly in the
Hanford Reach below Priest Rapids
Dam. In the Columbia River, P. robusta
is known from 17 locations, beginning
at approximately rm 20 (rkm 32) and
continuing for nearly 400 miles (649
km) upstream to just below Priest
Rapids Dam (Frest 2005a). Although
there have been several hundred
invertebrate samples collected in the
Columbia River over the past several
years, P. robusta has been found only in
a few of these samples (Frest 2005a).
Status Review Process
On April 20, 2005, we initiated
combined 12-month status reviews (70
FR 20512) of the petitioned springsnails,
as well as a 5-year review of the Idaho
springsnail under section 4(c)(2)(A) of
the Act, and solicited additional
information from the public on the
biology, ecology, distribution and status,
threats affecting the petitioned
springsnail species, and any ongoing or
planned conservation measures.
During the 60-day public comment
period, we contacted numerous Federal
and State resource agencies, interested
Tribal governments, and County
governments. On June 7, 2005, we
attended an information exchange
meeting with the State of Idaho Office
of Species Conservation, Idaho
Department of Fish and Game (IDFG),
Idaho Department of Environmental
Quality (IDEQ), U.S. Bureau of
Reclamation (BOR), U.S. Bureau of Land
Management (BLM), and others. After
this information exchange meeting, our
staff assimilated and analyzed all the
new information submitted during the
60-day public comment period, along
with the existing information already
obtained from published scientific
literature, unpublished technical
documents, and written and personal
communications. As part of our routine
Status Review process, we took this
synthesized information and created a
document titled: Draft Best Available
Biological Information for Four
Petitioned Springsnail Species from
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Idaho, Oregon, Washington, and
Wyoming (Draft BAI). The Draft BAI
represented our comprehensive, best
available scientific and commercial
information on the petitioned
springsnails.
On August 3, 2005, through a widely
distributed outreach effort that included
a news release, Dear Interested Party
letter, posting on the Service’s Web site,
and a request for peer review, we
opened an additional 30-day public and
peer review comment period on the
Draft BAI. After the public and peer
review, Service staff incorporated the
additional information and technical
corrections received, and wrote Version
2.0 Best Available Biological
Information for Four Petitioned
Springsnail Species from Idaho, Oregon,
Washington, and Wyoming (BAI). The
revised BAI constituted the peerreviewed state of knowledge with regard
to the taxonomy, biology, ecology,
distribution, and status of the four
petitioned springsnail species, now
combined as Pyrgulopsis robusta, and
was used throughout the remainder of
the Status Review process as the
primary source of best available
scientific and commercial data.
The Service utilized a structured
decision making model to assess the
available data. Based on an early
assessment of the degree of uncertainty
surrounding the population trends and
conservation status of Pyrgulopsis
robusta, the Service used two panels to
inform our recommended course. The
first panel (Expert Panel) was made up
of six scientists from outside the Service
with expertise in relevant fields,
including snail biology and ecology,
community ecology, population
ecology, stream ecology, aquatic
ecotoxicology, and regional water
quality. This Expert Panel met on
October 18–19, 2005, to discuss the
strengths and weaknesses of the various
data, hypotheses, and opinions relative
to the current status of P. robusta. The
Expert Panel only addressed the
scientific aspects of risk and threats, and
estimated the probable extinction risk to
P. robusta. A second ‘‘Managers Panel’’
of five Service managers and senior
biologists met on October 20–21, 2005,
to consider the Expert Panel’s input and
all other information necessary to
conduct an extinction risk assessment of
P. robusta. Information generated from
these two Panels was used in the
Service’s status review to assess threats
to, and evaluate the listing status of, P.
robusta. Further details about the
structured decision making process
used by the two panels are documented
in our administrative record for this
proposed rule.
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Inspection of the petition to delist the
Idaho springsnail, the petition to list the
Jackson Lake, Harney Lake, and
Columbia springsnails, and the
supporting information, administrative
finding, and other relevant materials
may be made in person, by
appointment, at the address listed above
(see ADDRESSES).
Summary of Factors Affecting the
Species
Section 4 of the Act and regulations
(50 CFR Part 424) promulgated to
implement the listing provisions of the
Act set forth the procedures for listing,
reclassifying, and delisting species. A
species may be listed as threatened or
endangered if one or more of the five
factors described in section 4(a)(1) of the
Act threaten the continued existence of
the species. A species may be delisted,
according to 50 CFR 424.11(d), if the
best scientific and commercial data
available substantiate that the species is
neither endangered nor threatened
because of: (1) Extinction; (2) recovery;
or (3) error in the original data, or the
data analysis, used for classification of
the species. For species that are being
considered for delisting, the analysis of
threats must include an evaluation of
threats that existed at the time of listing
and those that currently exist or that
could, with a reasonable degree of
likelihood, potentially affect the species
in the foreseeable future after its
delisting and the consequent removal of
the Act’s protections.
A. The Present or Threatened
Destruction, Modification, or
Curtailment of Its Habitat or Range
The 1992 final listing rule (57 FR
59244) described activities such as
proposed large hydroelectric dam
developments, peak-loading operations
of existing hydroelectric water projects,
small hydroelectric developments,
water pollution, and water diversions
whose cumulative effects threatened the
habitat and fragmented populations of
the Idaho springsnail (Pyrgulopsis
idahoensis). After reviewing the best
available scientific and commercial
information regarding present or
threatened destruction, modification, or
curtailment of the habitat or range of P.
robusta, we determined that the
principal habitat-related threats are not
proceeding at a rate that will threaten
the continued existence of the species
within the foreseeable future.
Dams and Reservoirs
Our 1992 listing of the Idaho
springsnail was based on information
that indicated that the species was
found only in permanent flowing waters
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of the mainstem Snake River, and that
its historic range had been reduced
nearly 80 percent, in large part by dam
and reservoir development and
operations.
Populations of Pyrgulopsis robusta
have been collected from various
habitats, including springs, river
reaches, and both lake and reservoir
locations (Bickell 1977, p. 33; Hershler
1998, p. 99; Richards and Lester 2002,
pp. 6–7; Stephenson et al. 2004, pp. 11,
21). In the Snake River in Idaho, where
P. robusta occurs over a range of 214
river miles (344 km), the greatest
number of live collections and the
highest percentages of P. robusta
occurrence are generally found in
flowing waters influenced by reservoirs
(Clark 2005). While extensive surveys
conducted in downstream reaches (i.e.,
below Hells Canyon) of the Snake River
(Shinn et al. 2001, pp. 80–82; Finni
2003b, p. 1; Richards et al. 2005, pp. 4–
5) and Columbia River basins (Frest and
Johannes 1995, p. 203) have not
documented the presence of
springsnails, springsnails have been
known to persist in habitats associated
with reservoirs (i.e., C.J. Strike and
Swan Falls). At the upstream end of
their range in C.J. Strike Reservoir,
abundant numbers of springsnails are
located at the mouth of a small tributary
(i.e., main-pool) and on the gravel
shores of the Bruneau River Arm, where
comparatively cool and flowing waters
(i.e., relative to the Snake River) of the
Bruneau River run into C.J. Strike
Reservoir (Stephenson et al. 2004, p.
21). In Swan Falls Reservoir, P. robusta
are found in the headwaters (i.e., the
nebulous upstream end of a reservoir
and downstream end of free-flowing
river) of the reservoir, but only one snail
has been collected (at rm 460; rkm 740)
in the main pool from the dam to 7
miles (11.2 km) upstream of the dam
(Clark 2005).
At the downstream end of Pyrgulopsis
robusta’s range in Idaho, the species’
known distribution ends immediately
above the Hells Canyon Complex at the
headwaters of Brownlee Reservoir
(approximately rm 340 (rkm 547)). The
Hells Canyon Complex includes three
large reservoirs (Brownlee, Oxbow, and
Hells Canyon) that are deep (two have
very steep sides) and whose waters
fluctuate on both a daily and annual
basis (Esch 2005). Surveys by the IPC in
and below the Hells Canyon Complex
have not yielded P. robusta (Finni
2003b, pp. 9, 19; Meyers and Foster
2003, pp. 17–18; Richards et al. 2005,
pp. 71–78, 103–149). The particular
habitat conditions of these reservoirs
may not be able to support P. robusta
and may also prevent successful
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downstream migration to suitable
habitat below the Hells Canyon
Complex (Shinn et al., 2001, p. 20;
Meyers and Foster 2003, pp. 18–20).
In Oregon and Washington,
Pyrgulopsis robusta has been
documented in the lower Columbia
River below Dalles and John Day Dams
and in their pools (Frest 2005a). These
collections were in areas where the flow
is greater and the river is shallower than
in the reservoir (Frest 2005a). In
southeastern Oregon, P. robusta was
found in the south fork of the Malheur
River (Hershler and Liu 2004, p. 79;
Frest 2005a). These collections were
reported to have been taken 60 miles
upstream of Warm Springs Dam in an
area of spring up-welling from the
hyporheic zone (area below the
streambed where water passes through
spaces between the rock and cobble)
(Frest 2005a, b).
Our current status review indicates
that Pyrgulopsis robusta is not restricted
to permanent free-flowing water; the
species also occurs in slower moving
reservoir reaches and also in areas with
and without spring inflow or upwelling
occurrences. Our previous concern, as
stated in the 1992 listing rule, regarding
the historic range of the species in the
Snake River having been reduced nearly
80 percent by dams and reservoirs, does
not apply to P. robusta. New
information collected on the Idaho
springsnail population’s life history,
distribution, and status has been
incorporated into this status review,
together with information about the
three other P. robusta populations
(Jackson Lake, Harney Lake, and
Columbia River). Much of this
information has been collected during
aquatic and mollusk surveys conducted
by the IPC in the Snake River and Frest
(2005 a, b) for the Columbia River and
southeast Oregon populations. The IPC
has been collecting information on
Idaho springsnail populations
throughout the Snake River since 1995.
Based on the results of these surveys
and laboratory studies, we now have a
much better understanding of the basic
life history as well as current
distribution and status of P. robusta in
the Snake River. These surveys have
documented that P. robusta is more
widely distributed in the Snake River
than originally described in the 1992
listing rule. IPC biologists have
surveyed over 400 river miles (644 km)
in the Snake River and have
documented the species at over 174
known locations over 214 river miles
(344 km), between rm 340 (rkm 547) and
rm 554 (rkm 892) (Clark 2005), a nearly
500 percent increase, or 179 river miles
(292 km), of its known range. In
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summary, P. robusta has been
determined to be more widely
distributed and to occur on a much
wider diversity of substrate types and
sizes, and in a greater variety of aquatic
habitats than was known at the time of
the Idaho springsnail’s listing in 1992.
The species occurs throughout long
reaches of the Snake River and
Columbia Rivers in areas that are
influenced by dams and reservoirs.
The 1992 listing rule discussed ‘‘peakloading, the practice of artificially
raising and lowering river levels to meet
short-term electrical needs by local runof-the-river hydroelectric projects,’’ as a
threat that ‘‘may adversely affect three
known populations of the Idaho
springsnail’’ (57 FR 59252). Certain
hydroelectric power generating
operational scenarios (e.g., water
storage, diversion, and peak-loading)
have been documented to have adverse
impacts on aquatic communities
(Armitage 1984, pp. 141–143; Brusven
1984, p. 167; Vaughn and Taylor 1999,
pp. 915–916; Watters 2000, p. 1). C.J.
Strike Dam is the primary peak-loading
hydroelectric facility in the Snake River,
yet Pyrgulopsis robusta persists in the
peak-loading-affected area (Clark 2005).
For example, the largest monitored
colony of P. robusta exists in the Snake
River approximately 3 river miles (4.8
km) downstream of C.J. Strike Dam
(Stephenson et al. 2004, p. 14). The
Expert Panel and Service’s Manager
Panel both acknowledged that because
colonies of P. robusta are widespread
and known to occur over a 214-mile
(344-km) stretch of the Snake River that
is subject to long-term, recurring peakloading and fluctuating flows, these
colonies are resilient and will likely
continue to persist into the foreseeable
future.
The effects of dams and reservoirs
have been suggested as barriers to
dispersal for Pyrgulopsis robusta.
Species that have limited distributions
and/or smaller, isolated populations
may have a higher risk of local
extirpations due to various threats and
demographic stochasticity (variability)
(Meffe et al. 1997, pp. 284–299; Vaughn
and Taylor 1999, p. 916; Fagan et al.
2002, p. 3250). Both the Expert Panelists
and Service’s Manager Panelists
acknowledged this risk for springsnails,
but did not expect these populations to
become extirpated due to possible
barriers to dispersal in the foreseeable
future.
Groundwater Pumping
Groundwater pumping is only a
concern for Pyrgulopsis robusta
populations in southeast Oregon.
Groundwater pumping for domestic use,
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agriculture, and industry may deplete
flows from groundwater-fed spring
systems by altering, modifying, or
curtailing habitats dependent on those
groundwater sources (Sada and Vinyard
2002, pp. 277–278).
The Oregon Water Resources
Department (OWRD) regulates water
development (OWRD 2005a), but very
little information is available for the
Malheur Basin or the Abert Lake Basin,
where the Harney Lake population of
Pyrgulopsis robusta is found. While
spring development and/or destruction
have been implicated in native species
declines in southeastern Oregon (Frest
and Johannes 1995, p. 196), we are not
aware of spring alterations,
modifications, or conservation efforts
that are affecting P. robusta in
southeastern Oregon. Although at least
one location previously containing P.
robusta in southeastern Oregon no
longer has springsnails (Hershler 1994,
p. 41; Frest and Johannes 1995, p. 196),
groundwater pumping can not be
explicitly linked to the springsnail’s
absence. In two OWRD observation
wells in the Malheur Basin,
groundwater levels seem to have been
relatively stable since 1960 (OWRD
2005b). We acknowledge that diversion
of springwater flows and groundwater
pumping can represent barriers to
dispersal and potentially isolate
populations of P. robusta. However,
these effects are limited to populations
only in southeast Oregon, and not
elsewhere in the species’ range.
Water Quality—Temperature, Nutrients,
and Chemical Stressors
The 1992 listing rule (57 FR 59244)
stated, ‘‘The quality of water in these
habitats has a direct effect on the
species survival. The species requires
cold, well-oxygenated unpolluted water
for survival. Any factor that leads to a
deterioration in water quality would
likely extirpate these taxa.’’
Numerous reaches of the Snake and
Columbia Rivers are classified as waterquality-impaired due to the presence of
one or more pollutants (e.g., total
phosphorous, sediments, total
coliforms) in excess of State or Federal
guidelines. Nutrient-enriched waters
primarily enter the Snake and Columbia
Rivers via springs, tributaries, fish farm
effluents, municipal waste treatment
facilities, and irrigation returns (U.S.
Environmental Protection Agency
(USEPA) 2002, pp. 4–20 to 4–22;
USFWS 2004, p. 1; U.S. Geological
Survey (USGS) 2005, p. 5). Irrigation
water returned to rivers is generally
warmer, contains pesticides or pesticide
byproducts, has been enriched with
nutrients from agriculture (e.g., nitrogen
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and phosphorous), and frequently
contains elevated sediment loads.
Pollutants in fish farm effluent include
nutrients derived from metabolic wastes
of the fish and unconsumed fish food,
disinfectants, bacteria, and residual
quantities of drugs used to control
disease outbreaks. Recent research
found elevated levels of fine sediments
and nitrogen as well as elevated levels
of trace elements, including zinc,
copper, cadmium, lead, and chromium,
immediately downstream of aquaculture
discharges (Falter and Hinson 2003, p.
53). Additionally, concentrations of
lead, cadmium, and arsenic were
detected in snails collected during a
research study in the Snake River
(Richards 2002). Researchers at the
USGS (1998, p. 15) detected
concentrations of some pesticides in
fish tissues, streams, irrigation canals,
and irrigation returns in the Snake River
Basin in concentrations exceeding the
aquatic-life criteria established by the
USEPA. While some effects of
pollutants, including metals and organic
compounds in stream organisms, are
documented in the literature (Naimo
1995, pp. 351–352; Clements 1999, pp.
1076–1078; Courtney and Clements
2002, pp. 1770–1773), the potential
impact of these contaminants on
Pyrgulopsis robusta has not been
studied and is unknown. However, P.
robusta has been documented to occur
downstream in these stretches of the
Snake River where municipal,
aquaculture, and agricultural discharges
occur.
In the upper Snake River Basin in
Wyoming, very low levels of ammonia,
nitrite and nitrate, phosphorus, trace
metals, and pesticides have been
detected in water quality assessments
(USGS 2004, p. 39). Polecat Creek,
which contains Pyrgulopsis robusta
(Riley et al. 2003, p. 6), was included in
Wyoming’s section 303(d) of the Clean
Water Act list of impaired waterbodies
due to fecal coliform contamination
(WDEQ 2004, pp. 1–91). However, water
quality in the upper Snake River Basin
in Wyoming is generally described as
good (USGS 2004, p. 38).
Changes in a river’s flow and depth as
a result of dams lead to changes in
sediment deposition dynamics and
thermal characteristics (Poff et al. 1997,
p. 773; Platts 1992, p. 2). Watertransported sediments that would be
flushed downstream and deposited in
pools, eddies, and other still water
environments under normal river flows
now settle in slow moving reservoir
waters (Poff et al. 1997, p. 773; Simons
1979, pp. 96, 100–104). Additionally,
drops in water velocity in reservoirs
may result in elevated surface water
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temperatures and reductions in
dissolved oxygen (USGS 2005, p. 11).
Pyrgulopsis robusta has adapted to, and
survives in, a relatively wide range of
temperatures within the Snake River
(Lysne 2003, p. 27). The IPC has
collected P. robusta in water
temperatures ranging from near freezing
to 80 degrees F (27 degrees C) (Clark
2005). While high temperatures may be
of concern for some aquatic snail
species, we are not aware that water
temperature limits growth,
reproduction, or survival of P. robusta
in any portion of its range. Pyrgulopsis
robusta is widespread and abundant,
occurring in a variety of water quality,
flow, and temperature ranges. Expert
and Manager Panels noted that water
quality has not significantly modified or
curtailed the habitat or range of P.
robusta to an extent that threatens the
continued existence of the species.
Grazing
Grazing by cattle has been suggested
to be a threat to Pyrgulopsis robusta
habitat in southeastern Oregon (Frest
and Johannes 1995, p. 196), but not in
other areas. However, little information
exists regarding the impact of livestock
grazing on the P. robusta in
southeastern Oregon. Since the mid
1980s, cattle have been excluded from
riparian areas, springs, and spring
creeks in both the Harney and Malheur
Lakes region (Burnside 2004). The
Expert and Manager panels agreed that
grazing does not appear to constitute a
threat to the continued existence of the
species since it is limited only to
portions of the southeastern Oregon
populations.
Summary of Factor A
In summary, Pyrgulopsis robusta is
distributed over a wide geographic area
and a wide range of aquatic habitats in
Idaho, Oregon, Washington, and
Wyoming. Based on new information,
previous concerns about the species
being restricted to permanent free
flowing water and a reduction in range
limiting its distribution or threatening
its existence are no longer valid. For
example, since the 1992 listing, P.
robusta in the Snake River has been
collected at 174 locations over 214 river
miles (342 km). We are not aware that
water temperature limits growth,
reproduction, or survival of P. robusta
in any portion of its range. Dam-induced
changes to large river habitats in the
Snake River or Columbia River may
create conditions that likely represent
barriers to P. robusta migration;
however, the species persists
throughout long reaches of these two
river systems in areas influenced by
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dams and hydroelectric operations.
Barriers to dispersal (i.e., isolated and
fragmented populations) were
considered a threat factor by the Expert
Panel for the southeastern Oregon
populations, but were considered
relatively insignificant in both the
Snake and Columbia Rivers. The fact
that P. robusta is often locally abundant,
resilient, and adaptable to a range of
extrinsic factors, contributes to the
determination that P. robusta is not in
danger of extinction within the
foreseeable future. Thus, based on the
best scientific and commercial data, we
conclude that the present or threatened
destruction, modification, or
curtailment of P. robusta’s habitat or
range is not a factor that threatens or
endangers the species throughout all or
a significant portion of its range.
B. Overutilization for Commercial,
Recreational, Scientific, or Educational
Purposes
Overutilization of Pyrgulopsis robusta
for commercial, recreational, or
scientific purposes was not considered
to be an applicable threat at the time of
the 1992 listing (57 FR 59242), and is
still not considered by the Expert Panel
and Service’s Manager Panel to be a
threat to P. robusta throughout all or a
significant portion of its range.
C. Disease or Predation
We have no information on the actual
effects of disease or parasites on
Pyrgulopsis robusta.
At the time of the 1992 listing, fish
predation was not considered to be a
major threat (57 FR 59242). There is
currently no information regarding the
threat of predation on the continued
existence of Pyrgulopsis robusta.
Predation on snails, in general, is
documented and is a natural occurrence
(Merrick et al. 1992, p. 231; McCarthy
and Fisher 2000, p. 387), but
information on the effects of predation
on P. robusta is limited. In the only
known account of predation by fish on
P. robusta, Beetle (1957, p. 17) reported
shells were found in the digestive tract
of a Roseyside sucker (Catostomus
fecundus) near Jackson Lake Dam,
Wyoming. A recent study of predation
ecology with Pyrgulopsis species failed
to observe predation by native crayfish
(Pacifasticus spp.) (Lysne and Koetsier
2001, p. 6).
The Expert Panel did not identify
disease or predation as a significant
threat, but information is lacking to
draw any definitive conclusions about
risks to Pyrgulopsis robusta due to
predation. Based on the best scientific
and commercial data available, we
conclude that disease and predation are
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D. The Inadequacy of Existing
Regulatory Mechanisms
In the 1992 Idaho springsnail listing
rule (57 FR 59244), nutrient loading and
pollution in the middle Snake River
were identified as areas of concern. We
stated that it was unlikely that the
downward trend in water quality would
be reversed any time soon, because it
would take several years before any
recommendations to improve water
quality, as outlined in comprehensive
resource management plans for the
Snake River, were fully implemented
through local, State, and Federal
programs and efforts. However, since
the 1992 listing rule, some water quality
improvements have been realized in
localized reaches of the Snake River,
primarily with regard to sediment and
phosphorus reduction (Buhidar 2005).
These improvements are more fully
discussed in the Water Quality
Management section below.
Based on our status review, we
describe various regulatory mechanisms
implemented by State and Federal
resource agencies to protect Pyrgulopsis
robusta and its habitat. Federal agency
regulations are generally consistent
across States, but State regulations may
differ considerably with regard to
similar natural resource issues.
Analogous State natural resource
agencies exist in Idaho, Oregon,
Washington, and Wyoming.
Wildlife Conservation Statutes and
Plans
Washington has the comprehensive
statutory authority and mandate to
‘‘preserve and protect’’ all wildlife,
including invertebrates such as
Pyrgulopsis robusta, within its borders
(Revised Code of Washington
77.04.012). The Idaho Department of
Fish and Game (IDFG) developed a
Comprehensive Wildlife Conservation
Strategy (Idaho Strategy) that lists P.
robusta as a ‘‘species of greatest
conservation need’’ (IDFG 2005, p. 413).
For example, Pyrgulopsis robusta
conservation will be considered when
IDFG engages other States, Federal
agencies, and other conservation
partners on proposed activities affecting
Snake River habitats (e.g., boat ramp
construction). The Idaho Natural
Heritage Program lists Idaho springsnail
as a species of concern, the Oregon
Natural Heritage Program lists Columbia
and Harney Lake springsnails as species
of concern (ODFW 2005, p. 354), and in
Wyoming, the Jackson Lake springsnail
is also listed as a species of concern
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(WGFD 2005, p. 15). These State
wildlife conservation strategies and
plans are useful to land managers
because they provide the best available
information for species of greatest
conservation need and allow these
managers to make informed decisions
about land use changes.
Water Quality Management
There are various State-managed
water quality programs within the range
of Pyrgulopsis robusta in Idaho,
Washington, Wyoming, and Oregon.
These programs are tiered off of the
Clean Water Act (CWA), which requires
States to establish water quality
standards that provide for the protection
and propagation of fish, shellfish, and
wildlife, and recreation in and on the
water (‘‘fishable/swimmable’’). In
addition, as part of the CWA, States
must also include an antidegradation
policy that protects waterbody uses, and
high-quality waters. In Idaho,
Washington, Wyoming, and Oregon,
point source discharges are regulated
through the National Pollutant
Discharge Elimination System (NPDES)
program. These NPDES permits are
written to meet all applicable water
quality standards established for a
waterbody to protect human health and
aquatic life.
Idaho has established water quality
standards (e.g., water temperature and
dissolved oxygen) for the protections of
cold-water biota (e.g., invertebrate
species) in many reaches of the Snake
River. Although conditions within the
river periodically exceed these limits
during the summer months (USGS 2005,
pp. 7–12), Pyrgulopsis robusta has been
collected in water temperatures ranging
from near freezing to 80 degrees F (27
degrees C) (Clark 2005). While high
temperatures may be of concern for
some aquatic snail species, water
temperature does not seem to limit
growth, reproduction, or survival of P.
robusta in any portion of its range.
Waters that do not meet standards due
to point- and non-point source pollution
are listed on USEPA’s 303(d) list of
impaired water bodies. States must
submit to USEPA a 303(d) list (water
quality-limited waters) and a 305(b)
report (status of the State’s waters) every
two years. Water quality improvements
with regard to point and non-point
sources have been realized in localized
reaches of the Snake River where P.
robusta occurs (Buhidar 2005),
primarily with regard to sediment and
phosphorus criteria. The IDEQ, under
authority of the State Nutrient
Management Act, is coordinating efforts
to identify and quantify contributing
sources of pollutants (including nutrient
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and sediment loading) to the Snake
River basin via the Total Maximum
Daily Load (TMDL) approach. TMDLs
are developed, adopted, and
implemented within State Agricultural
Water Quality Program, CWA section
401 Certification, BLM Resource
Management Plans, the State Water
Plan, and local ordinances.
In Oregon, point- and non-point
source pollution is managed by
Oregon’s Department of Environmental
Quality (ODEQ). TMDLs for several
stream reaches are in development for
the Malheur River Basin where
Pyrgulopsis robusta exists. TMDLs
establish mechanisms to address point
and non-point sources to bring these
reaches into compliance with water
quality standards.
In Washington, the State’s Department
of Ecology (WECY) has a mandate to
manage point and non-point sources of
pollution entering Washington’s waters
(WECY 2005). Non-point sources of
pollution are regulated by numerous
State of Washington statutes (WECY
2005), and managed primarily through
Washington’s Water Quality
Management Plan to Control Non-point
Source Pollution (Plan), published in
2000. Pyrgulopsis robusta is found in
the Columbia River, and the Plan may
indirectly benefit the springsnails that
occur there.
In Wyoming, Pyrgulopsis robusta
exists within waters that occur in
National Parks and are designated as
Class 1 or ‘‘outstanding waters’’ by the
Wyoming Department of Environmental
Quality. Maintaining this designation is
one of the National Park Service’s
highest priorities (USGS 2004, p. 2). We
are not aware of any proposals to
modify these designations or of
activities that would impair these water
bodies.
Federal Land Management
Many large scale Federal management
plans (e.g., U.S. Forest Service Land and
Resource Management Plans, U.S.
Bureau of Land Management (BLM)
Resource Management Plans, National
Wildlife Refuge Comprehensive
Conservation Plans, and Interior
Columbia Basin Ecosystem Management
Plan) promote conservation of aquatic
and terrestrial habitats, including those
on which Pyrgulopsis robusta depends.
Much of the Federal lands adjacent to
the Snake River in Wyoming, Idaho,
Oregon, and Washington are managed
by the BLM. Resource Management
Plans (RMPs) that guide BLM resource
management include provisions to
protect water quality and riparian
habitats. The Service and the BLM in
Idaho have finalized a Conservation
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Agreement (USBLM 2006, pp. 1–11) that
commits the BLM to carry out specific
actions to assess status and distribution
of P. robusta in areas affected by
management actions and also to modify
those actions to avoid and minimize
impacts to the species in the Snake
River. In addition, BLM has completed
Endangered Species Act section 7
consultations for some actions that may
affect P. idahoensis, now known as P.
robusta. The BLM’s Boise and Twin
Falls Districts have completed a joint
section 7 consultation for ongoing
livestock grazing activities in allotments
adjacent to P. robusta habitats in the
Snake River. Under that consultation,
the BLM and grazing permitees have
implemented actions to reduce the
amount of shoreline grazing and
grazing-related sediment, thereby
reducing the risk of take of P. robusta
resulting from livestock management.
Water Rights and Operations
In Idaho, there have been
improvements in Snake River water
management since the time of listing the
Idaho springsnail in 1992 (57 FR 59244).
Portions of the Snake River are
temporarily protected from further
allocation of consumptive use water
rights (Barker et al. 2005) by order of the
Director of the Idaho Department of
Water Resources, although this does not
preclude future water diversion or
consumption projects within the range
of Pyrgulopsis robusta in the Snake
River of Idaho. For the other geographic
areas where P. robusta occurs, we are
not aware of any State-sponsored
programs restricting allocation of
consumptive use water rights.
The U.S. Bureau of Reclamation
(BOR) operates numerous water projects
in the Snake River basin and is involved
in a variety of fish and wildlife
conservation efforts through a number
of different programs in Oregon,
Washington, and Idaho (USBOR 2005).
The BOR has conducted numerous
surveys for sensitive mollusks for
several years (USBOR 2002, p. 2; 2003,
p. 2; 2004, p. 2). Pyrgulopsis robusta has
not been found in the upper reaches of
the Snake River. The BOR has
developed 10-year Resource
Management Plans designed to create a
balance of resource development,
recreation, and protection of natural and
cultural resources for the lands and
waters they manage. These plans outline
resource management policies and
actions that will be implemented to
protect natural resources (e.g., sensitive
mollusk species) over each plan’s 10year life (USBOR 2005).
The U.S. Army Corps of Engineers
(USACE) operates several hydroelectric
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projects on the Columbia River within
the known range of Pyrgulopsis robusta,
including John Day, Dalles, and
Bonneville Dams. Since passage of the
National Environmental Policy Act of
1969, environmental protection has
been an important mission for the
Northwestern Division of the Corps
(USACE 2005). Since legislation passed
in 1990 establishing environmental
protection as one of the primary
missions of water resource projects, the
Corps has taken steps to ensure that
projects meet Federal, State, and local
environmental requirements (USACE
2005).
A Settlement Agreement between the
IPC and Service concerning the
relicensing of IPC’s mid-Snake and C.J.
Strike hydroelectric projects (IPC and
USFWS 2004) requires IPC to
implement studies to assess effects on
two listed Snake River aquatic snails,
including Pyrgulopsis robusta, from
operation of hydroelectric dams. The
1992 listing rule stated that proposals
for numerous small hydroelectric
projects to be developed on remaining
free-flowing portions of the middle
Snake River within the species’ range,
threatened the Idaho springsnail.
However, those proposals have
subsequently been withdrawn or were
not approved by the Federal Energy
Regulatory Commission (FERC) (Barker
et al. 2005), reducing the likelihood of
new FERC licensed hydroelectric
projects impacting P. robusta.
Summary of Factor D
A wide variety of regulatory
mechanisms managed by State and
Federal resource agencies are in place to
manage and protect Pyrgulopsis robusta
and the habitats upon which it depends.
Federal land management plans address
conservation of P. robusta habitats, and
Federal and State agencies are managing
water projects to minimize impacts on
P. robusta and protect the water quality
where the species occurs. Water
withdrawals for the allocation of
consumptive water use in the Snake
River basin have been halted through a
temporary moratorium by the State of
Idaho. Additionally, IPC hydroelectric
projects on the Snake River in Idaho
have begun to address P. robusta
management needs via specific
commitments in recent Settlement
Agreements. Given that P. robusta
occurs as multiple populations
distributed over a wide geographic area,
and a wide range and variety of habitat
types, the variety of State and Federal
regulatory mechanisms that directly and
indirectly provide conservation benefits
for P. robusta are generally considered
adequate.
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E. Other Natural or Manmade Factors
Affecting Its Continued Existence
Numerous non-native and invasive
species have become established
throughout the range of Pyrgulopsis
robusta, and others threaten to become
established; however, their impacts on
native species and ecosystems have not
been well studied or understood. (Frest
and Johannes 2000, p. 1; Anderson
2004, pp. 15–18; Sytsma et al. 2004, pp.
33–34).
In the 1992 listing rule (57 FR 59244)
for the Idaho springsnail, we stated that
the New Zealand mudsnail
(Potamopyrgus antipodarum) was a
potential threat to the Idaho springsnail.
The New Zealand mudsnail was
discovered in North America in 1987 in
the Snake River, and has spread rapidly
(Bowler 1991, p. 175; Richards and
Lester 2003, p. 1; Richards et al. 2004,
p. 114). The New Zealand mudsnail
appears to flourish in warm waterbodies
in Wyoming and Montana on substrates
of silt to cobbles (Hall et al. 2003, p.
407; Cada 2004, p. 29), but is also
reported to reach high densities within
the much cooler waters of the Snake
River (Clark et al. 2005, p. 17). The wide
physical and physiological tolerances of
the New Zealand mudsnail allow it to
thrive in various habitats (Richards et al.
2001, pp. 375, 378; Hall et al. 2003, p.
408). The ability of the New Zealand
mudsnail to occupy numerous habitat
types, including those typically
occupied by native snails (Richards et
al. 2001, pp. 375, 378; Richards 2004,
pp. 137–139), does not always provide
a competitive advantage for the New
Zealand mudsnail in interactions with
native species (Cowie 2004).
In the Greater Yellowstone Ecosystem,
researchers found evidence that New
Zealand mudsnails limit the
colonization of, and may influence the
large-scale distribution of, other
macroinvertebrates (Kerans et al. 2005,
p. 135). Research in Wyoming has
demonstrated that New Zealand
mudsnails have reduced densities of
Pyrgulopsis robusta in Polecat Creek in
Yellowstone National Park, but P.
robusta and New Zealand mudsnails
continue to co-exist (Riley et al. 2003,
pp. 16–18; Gustafson 2005, pp. 7–8).
The threat the New Zealand mudsnail
poses to P. robusta remains uncertain.
However, the New Zealand mudsnail
does not appear to currently endanger or
threaten P. robusta throughout all or a
significant portion of its range.
The Expert Panel and Service’s
Manager Panel identified the threat of
non-native species, including the New
Zealand mudsnail, to Pyrgulopsis
robusta’s survival as low. Both panels
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identified the lack of information about
non-native species interactions with P.
robusta as an area of uncertainty.
However, direct cause and effect
information that non-native species are
endangering or threatening P. robusta
populations does not exist.
Thus, based on the best scientific and
commercial data available, we have
concluded that other natural and
manmade factors do not endanger or
threaten Pyrgulopsis robusta throughout
all or a significant portion of its range.
Summary of Threats Section
Evidence collected since the Idaho
springsnail was listed in 1992 as
endangered (57 FR 59244) indicates
Pyrgulopsis idahoensis no longer
constitutes a distinct species. The
revised species, Pyrgulopsis robusta, is
a combined taxon composed of four
previously regarded as taxonomically
distinct springsnails—the Idaho,
Jackson Lake, Harney Lake, and
Columbia River springsnails.
Pyrgulopsis robusta populations in
the Columbia and Snake Rivers have
relatively high abundance and occur as
multiple populations distributed over a
wide geographic area. The Columbia
River population of P. robusta is
currently known from 17 locations
starting from river mile 20 (rkm 32) and
continuing for nearly 400 river miles
(644 rkm) upstream to just below Priest
Rapids Dam. In the Snake River, P.
robusta is more widely distributed than
originally cited in the 1992 listing rule
and has been documented at over 174
known locations, over 214 river miles
(344 km). The species occurs in a range
of habitat types, and is resilient to
changes in flow and water quality.
Extant populations occur in various
habitats, including springs, and river
reaches characterized by a wide range of
flow conditions, and both occur in lake
and reservoir locations. Pyrgulopsis
robusta has adapted to, and survives in,
a relatively wide range of temperatures.
Fluctuating water temperatures likely
do not limit growth, reproduction, or
survival of P. robusta in any portion of
its range. Adequate existing regulatory
mechanisms contributing to P. robusta
conservation include water quality
regulations and FERC hydropower
Settlement Agreements. At this time P.
robusta exists in multiple populations
in the States of Oregon, Washington,
Idaho, and Wyoming and is expected to
persist into the future. We evaluated the
best available scientific and commercial
data regarding status of and threats to
the newly described P. robusta, and
determined that the species is not in
danger of extinction, nor is it likely to
become endangered in the foreseeable
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future throughout all or a significant
portion of its range, and therefore does
not meet the definition of threatened or
endangered.
Finding
We have carefully assessed the best
scientific and commercial information
available regarding the past, present,
and future threats faced by this species.
We reviewed the petitions, available
published and unpublished scientific
and commercial information, and
information submitted to us during the
public comment period following our
90-day petition findings. This finding
reflects and incorporates information we
received during the public comment
period and responds to significant
issues (i.e., incorporates appropriate
information raised in comments
regarding P. robusta taxonomy, life
history, distribution, status, and
threats). We also consulted with
recognized springsnail experts and
Federal and State resource agencies.
Based on this review, we find that (1)
Based on a change in taxonomic status,
the Idaho springsnail is no longer
considered a listable entity, and
therefore its delisting is warranted; (2)
based on a change in taxonomic status,
the Jackson Lake, Harney Lake, and
Columbia springsnails are no longer
considered listable entities, and
therefore their listing is not warranted;
and (3) listing of the combined taxon, P.
robusta, is not warranted because P.
robusta is distributed over a wide
geographic area and range of aquatic
habitats, is often locally abundant, and
appears to be resilient and adaptable to
a range of factors affecting it, including
varying water temperatures, flow
conditions, and water chemistry, and is
therefore not threatened with
endangerment throughout all or a
significant portion of its range.
In making this determination, we
have followed the procedures set forth
in section 4(a)(1) of the Act and
regulations implementing the listing
provisions of the Act (50 CFR part 424).
While the finding reflects the analyses
conducted to fulfill our responsibilities
under sections 4(b)(3)(A) (status review)
and 4(c)(2) (5-year review) of the Act,
we request that you submit any new
information, whenever it becomes
available, for this species concerning
status and threats. We intend that any
action for the P. robusta be as accurate
as possible. Therefore, we will continue
to accept additional information and
comments from all concerned
governmental agencies, the scientific
community, Native American Tribes,
industry, or any other interested party
concerning this finding.
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Delisting Proposal
Section 4(a)(1) of the Act and
regulations (50 CFR part 424) issued to
implement the listing provisions of the
Act set forth the procedures for adding
species to, or removing them from,
Federal lists. The regulations at 50 CFR
424.11(d) state that a species may be
delisted if: (1) The species is extinct or
has been extirpated from its previous
range; (2) the species has recovered and
is no longer endangered or threatened;
or (3) investigations show that the best
scientific or commercial data available
when the species was listed, or the
interpretation of such data, were in
error. Since the time of the Idaho
springsnail listing, additional study has
shown that Pyrgulopsis idahoensis is
not a distinct species, but is now part
of a combined taxon (Pyrgulopsis
robusta) composed of springsnails
occurring in the States of Wyoming,
Oregon, Idaho, and Washington. Our
evaluation of P. robusta status and
threats indicates it does not qualify for
protection under the Act. After a review
of the best available scientific and
commercial data, we are proposing to
remove Pyrgulopsis idahoensis from the
List of Endangered and Threatened
Wildlife in 50 CFR 17.11.
Effects of the Proposed Rule
This action proposes to remove
Pyrgulopsis idahoensis from the List of
Endangered and Threatened Wildlife. If
this proposed rule is finalized, the
prohibitions and conservation measures
provided by the Act would no longer
apply to P. robusta, with which P.
idahoensis has been combined.
Interstate commerce, import, and export
of this species would not be prohibited
under the Act. In addition, Federal
agencies would no longer be required to
consult under section 7 of the Act on
actions which may affect this species.
There is no designated critical habitat
for this species, and therefore the
proposed rule has no effect on critical
habitat.
Public Hearing
The Act provides for one or more
public hearings on this proposal, if
requested. Requests must be filed by the
date specified in the DATES section.
Such requests must be made in writing
and addressed to the Field Supervisor,
Snake River Fish and Wildlife Office,
1387 S. Vinnell Way, Room 368, Boise,
ID 83709.
Peer Review
In accordance with our peer review
policy published in the Federal Register
on July 1, 1994 (59 FR 34270), we will
seek expert opinions of at least three
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appropriate and independent specialists
regarding this proposed rule. The
purpose of such review is to ensure that
our delisting proposal is based on
scientifically sound data, assumptions,
and analyses. We will send copies of
this proposed rule to these peer
reviewers immediately following
publication in the Federal Register. We
will consider all peer review comments
received during preparation of a final
rulemaking. Accordingly, the final
decision may differ from this proposed
rule.
Clarity of the Rule
Executive Order 12866 requires each
agency to write regulations and notices
that are easy to understand. We invite
your comments on how to make this
proposed rule easier to understand,
including answers to questions such as
the following: (1) Are the requirements
in the proposed rule clearly stated? (2)
Does the proposed rule contain
technical jargon that interferes with the
clarity? (3) Does the format of the
proposed rule (grouping and order of
the sections, use of headings,
paragraphing, and so forth) aid or
reduce its clarity? (4) Is the description
of the notice in the SUPPLEMENTARY
INFORMATION section of the preamble
helpful in understanding the proposed
rule? (5) What else could we do to make
this proposed rule easier to understand?
Send a copy of any comments on how
we could make this proposed rule easier
to understand to: Office of Regulatory
Affairs, Department of the Interior,
Room 7229, 1849 C Street, NW.,
Washington, DC 20240. You may e-mail
your comments to this address:
Exsec@ios.doi.gov.
cprice-sewell on PROD1PC66 with PROPOSALS
Paperwork Reduction Act of 1995 (44
U.S.C. 3501 et seq.)
Office of Management and Budget
(OMB) regulations at 5 CFR 1320
implement provisions of the Paperwork
Reduction Act (44 U.S.C. 3501 et seq.),
which requires that interested members
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of the public and affected agencies have
an opportunity to comment on agency
information collection and
recordkeeping activities (5 CFR
1320.8(d)). The OMB regulations at 5
CFR 1320.3(c) define a ‘‘collection of
information’’ as the obtaining of
information by or for an agency by
means of identical questions posed to,
or identical reporting, recordkeeping, or
disclosure requirements imposed on, 10
or more persons. Furthermore, 5 CFR
1320.3(c)(4) specifies that ‘‘10 or more
persons’’ refers to the persons to whom
a collection of information is addressed
by the agency within any 12-month
period. This proposal does not contain
any new collections of information that
require OMB approval under the
Paperwork Reduction Act.
National Environmental Policy Act
The Service has determined that
Environmental Assessments and
Environmental Impact Statements, as
defined under the authority of the
National Environmental Policy Act of
1969, need not be prepared in
connection with actions adopted under
section 4(a) of the Act. We published a
notice outlining our reasons for this
determination in the Federal Register
on October 25, 1983 (48 FR 49244). This
assertion was upheld in the courts of the
Ninth Circuit (Douglas County v.
Babbitt, 48 F.3d 1495 (9th Cir. Ore.
1995), cert. denied 116 S. Ct. 698 (1996).
Government-to-Government
Relationship With Tribes
In accordance with the President’s
memorandum of April 29, 1994,
‘‘Government-to-Government Relations
With Native American Tribal
Governments’’ (59 FR 22951), Executive
Order 13175, and the Department of the
Interior’s manual at 512 DM 2, we
readily acknowledge our responsibility
to communicate meaningfully with
recognized Federal Tribes on a
government-to-government basis.
Therefore, we will solicit information
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from Native American Tribes during the
comment period to determine potential
effects on them or their resources that
may result from the delisting of the
Idaho springsnail, and we will fully
consider their comments on the
proposed rule submitted during the
public comment period.
References
A complete list of all references cited
is available on request from the Snake
River Fish and Wildlife Office (see
ADDRESSES).
Author
The authors of this document are staff
of the U.S. Fish and Wildlife Service,
Snake River Fish and Wildlife Office,
Boise, Idaho.
List of Subjects in 50 CFR Part 17
Endangered and threatened species,
Exports, Imports, Reporting and
recordkeeping requirements,
Transportation.
Proposed Regulation Promulgation
Accordingly, we hereby propose to
amend part 17, subchapter B of chapter
I, title 50 of the Code of Federal
Regulations, as set forth below:
PART 17—[AMENDED]
1. The authority citation for part 17
continues to read as follows:
Authority: 16 U.S.C. 1361–1407; 16 U.S.C.
1531–1544; U.S.C. 4201–4245; Pub. L. 99–
625, 100 Stat. 3500; unless otherwise noted.
§ 17.11
[Amended]
2. Amend § 17.11(h) by removing the
entry ‘‘Springsnail, Idaho (Fontelicella
idahoensis)’’ under SNAILS from the
List of Endangered and Threatened
Wildlife.
Dated: September 20, 2006.
Marshall Jones,
Acting Director, Fish and Wildlife Service.
[FR Doc. E6–15915 Filed 9–27–06; 8:45 am]
BILLING CODE 4310–55–P
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[Federal Register Volume 71, Number 188 (Thursday, September 28, 2006)]
[Proposed Rules]
[Pages 56938-56948]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E6-15915]
-----------------------------------------------------------------------
DEPARTMENT OF THE INTERIOR
Fish and Wildlife Service
50 CFR Part 17
RIN 1018-AU66
Endangered and Threatened Wildlife and Plants; 12-Month Finding
on a Petition To Delist the Idaho Springsnail; 12-Month Finding on a
Petition To List the Jackson Lake Springsnail, Harney Lake Springsnail,
and Columbia Springsnail; and Proposed Rule To Remove the Idaho
Springsnail From the List of Threatened and Endangered Wildlife
AGENCY: Fish and Wildlife Service, Interior.
ACTION: Notice of two 12-month petition findings and a proposed rule to
delist the Idaho springsnail (Pyrgulopsis idahoensis).
-----------------------------------------------------------------------
SUMMARY: We, the U.S. Fish and Wildlife Service (USFWS, Service, or
we), under the Endangered Species Act of 1973, as amended (Act),
announce combined 12-month findings on a petition to delist the
endangered Idaho springsnail (Pyrgulopsis idahoensis) and a petition to
list the Jackson Lake springsnail (P. robusta), Harney Lake springsnail
(P. hendersoni), and Columbia springsnail (P. species A (unnamed)).
Evidence collected subsequent to the December 14, 1992, listing (USFWS
1992, pp. 59244-59527 (57 FR 59244)) of the Idaho springsnail indicates
it no longer constitutes a distinct species. It is now described as the
Jackson Lake springsnail (P. robusta), a single taxon, composed of four
previously distinct springsnail species (Idaho, Jackson Lake, Harney
Lake, and Columbia springsnails), and therefore we are proposing to
remove
[[Page 56939]]
the Idaho springsnail from the Federal List of Endangered and
Threatened Wildlife. We evaluated the best available scientific and
commercial information regarding the status of, and threats to, the
newly described P. robusta, and determined that the threats to the
species do not warrant its listing at this time. Additionally, based on
our status review of P. robusta, we also find that listing the Jackson
Lake springsnail, Harney Lake springsnail, and Columbia springsnail as
separate species is not warranted.
DATES: The 12-month findings on the delisting and listing petitions
announced in this notice were made on September 28, 2006. We request
that new information be submitted to us concerning the status of, or
threats to, Pyrgulopsis robusta, whenever it becomes available.
We will accept comments from all interested parties regarding the
proposal to delist the Idaho springsnail until November 27, 2006. We
must receive requests for public hearings on or before November 13,
2006.
ADDRESSES: Comments may be submitted on the proposed rule to delist the
Idaho springsnail by any of the following methods. Please include RIN
1018-AU66 in any subject line.
E-mail: fws1srbocomments@fws.gov.
Fax: (208) 378-5262.
Hand carry, Postal Delivery, or Courier: Snake River Fish
and Wildlife Office, U.S. Fish and Wildlife Service, 1387 S. Vinnell
Way, Room 368, Boise, ID 83709.
Federal Rulemaking Portal: https://www.regulations.gov.
Follow the instructions for submitting comments.
Please see the Public Comments Solicited section below for file
format and other information about electronic filing.
FOR FURTHER INFORMATION CONTACT: The Snake River Fish and Wildlife
Office by mail at the above address; by telephone at 208/378-5243; by
facsimile at 208/378-5262; or by electronic mail at:
fw1srbocomment@fws.gov.
SUPPLEMENTARY INFORMATION:
Public Comments Solicited
We intend that any final action resulting from this proposal will
be as accurate and effective as possible. Therefore, comments or
suggestions from the public, other concerned governmental agencies,
Native American Tribes, the scientific community, industry, or any
other interested party concerning this proposed rule are hereby
solicited. Please note that comments merely stating support or
opposition to the actions under consideration without providing
supporting information, although noted, will not be considered in
making a determination, because section 4(b)(1)(A) of the Act directs
that determinations as to whether any species is a threatened or
endangered species shall be made ``solely on the basis of the best
scientific and commercial data available.''
You may submit materials concerning this proposal by any one of
several methods (see ADDRESSES section). Please submit Internet
comments to fws1srbocomments@fws.gov in ASCII file format and avoid the
use of special characters or any form of encryption. Please also
include ``RIN 1018-AU66'' in your e-mail subject header and your name
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termination of the public comment period.
Our practice is to make comments, including names and home
addresses of respondents, available for public review during regular
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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 rulemaking 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.
Comments and other information received, as well as supporting
information used to write this rule, will be available for public
inspection, by appointment, during normal business hours at the above
address. In making a final decision on this proposal, we will take into
consideration any additional information we receive. Such
communications may lead to a final regulation that differs from this
proposal.
Background
Section 4(b)(3)(B) of the Endangered Species Act of 1973, as
amended (Act) (16 U.S.C. 1531 et seq.) requires that, for any petition
to revise the List of Threatened and Endangered Species that contains
substantial scientific and commercial information that suggests a
change in status may be warranted, we make a finding within 12 months
of the date of the receipt of the petition on whether the petitioned
action is: (a) Not warranted; (b) warranted; or (c) warranted, but the
immediate proposal of a regulation implementing the petitioned action
is precluded by other pending proposals to determine whether a species
is threatened or endangered, and expeditious progress is being made to
add or remove qualified species from the List of Threatened and
Endangered Species. Such 12-month findings are to be promptly published
in the Federal Register. In addition, section 4(b)(3)(C) of the Act
requires that a petition for which the requested action is found to be
warranted but precluded shall be treated as though resubmitted on the
date of such finding (i.e., requiring a subsequent finding to be made
within 12 months).
Previous Federal Action
We published the final rule listing the Idaho springsnail as
endangered on December 14, 1992 (57 FR 59244). In that rule, we
described range reduction, continued adverse habitat modification,
deteriorating water quality from multiple sources, and the appearance
of the invasive New Zealand mudsnail (Potamopyrgus antipodarum) as the
major threats to the species. We have not designated critical habitat
for the Idaho springsnail.
On June 28, 2004, we received a petition from the Idaho Office of
Species Conservation and the Idaho Power Company (IPC) requesting that
the Idaho springsnail be delisted based on a recent taxonomic revision
of the species. The petitioners also provided new Idaho springsnail
scientific information, and contrasted this new information with
information used in the 1992 Idaho springsnail listing decision (57 FR
59244). The petitioners stated that most, if not all, threats to Idaho
springsnail identified in the 1992 listing rule have been eliminated,
are being actively addressed by State and private entities, or are not
relevant, based on new scientific information.
On August 5, 2004, we received a petition from Dr. Peter Bowler,
the Biodiversity Conservation Alliance, the Center for Biological
Diversity, the Center for Native Ecosystems, the
[[Page 56940]]
Western Watersheds Project, and the Xerces Society, requesting that the
Jackson Lake springsnail, Harney Lake springsnail, and Columbia
springsnail be listed as either threatened or endangered species, and
as either individual species or combined as the new species,
Pyrgulopsis robusta. This listing petition cited habitat loss and
degradation from development impacting springs, domestic livestock
grazing, and groundwater withdrawal, among other factors, as threats to
the continued existence of these three springsnail species. The listing
petition also discussed the recent springsnail taxonomic revision and
acknowledged that the Jackson Lake springsnail, Harney Lake
springsnail, Columbia springsnail, and Idaho springsnail may be one
species (P. robusta), but contended that, whether considered
individually or as one species, all four springsnails warranted the
protection of the Act.
On April 20, 2005, we published combined 90-day petition findings
(USFWS 2005, pp. 20512-20514 (70 FR 20512)), stating that both
petitions provided substantial information suggesting that delisting of
the Idaho springsnail, or listing of Jackson Lake springsnail, Harney
Lake springsnail, and Columbia springsnail, may be warranted.
Species Information
The Idaho springsnail (Pyrgulopsis idahoensis; Hydrobiidae) was
first described by Pilsbry (1933, pp. 11-12) and placed in the genus
Amnicola. Greg and Taylor (1965, pp. 103-110) established the new genus
Fontelicella and then placed P. idahoensis in the subgenus Natricola,
created in 1965 (Greg and Taylor 1965, pp. 108-109). Natricola
contained the Idaho springsnail, the Harney Lake springsnail (P.
hendersoni), and the Jackson Lake springsnail (P. robusta). After
several taxonomic revisions, the subgenus Natricola was placed in
synonymy with the genus Pyrgulopsis by Hershler and Thompson (1987, p.
29). Pyrgulopsis is the largest genus of freshwater mollusks in North
America, comprised of over 120 described species (Liu and Hershler
2005, p. 284). The greatest diversity of the genus occurs in the Great
Basin of the western United States (Hershler and Sada 2000, p. 367;
Hershler and Sada 2002, p. 255).
In 2004, Hershler and Liu (2004, pp. 78-79) revised the taxonomic
status of four springsnails Pyrgulopsis idahoensis, P. hendersoni, P.
robusta, and the Columbia springsnail (P. species A (unnamed)), by
placing all four springsnails into the oldest available taxon of the
four revised species, P. robusta (Jackson Lake springsnail, Walker
1908, p. 97). All four species were considered members of the subgenus
Natricola. Members of the subgenus Natricola are very similar in size
and shape, being distinguished primarily by the morphology of the
shell. The authors reviewed morphological characters, mitochondrial DNA
sequences, and nuclear DNA sequences to establish the need for
taxonomic status change.
Several morphological metrics, including the position of the callus
(thickened portion) on the operculum (serves as a cover for the opening
in the shell); the shape of the central cusp of the central teeth; the
number of cusps on central teeth; notching of inner marginal teeth;
number of cusps on outer marginal teeth; the male penile features; and
female genitals, did not differ significantly among the four
springsnail species (Hershler and Liu 2004, pp. 70-75). Five shell
parameters were significantly heterogeneous in a comparison of the four
springsnail species. In only one case did a single springsnail species
differ significantly from the other three; the Idaho springsnail
differed significantly from the other three springsnail species for the
ratio of shell height to height of body whorl (Hershler and Liu 2004,
p. 71).
To construct species topologies, Hershler and Liu (2004, pp. 67-69)
sequenced selected genes of four springsnail species, Pyrgulopsis
robusta, P. idahoensis, P. hendersoni, and P. species A (unnamed), as
well as congeners P. imperialis, P. intermedia, P. kolobensis, and P.
species B (unnamed). The mitochondrial DNA data revealed little
difference in the partial CO1 gene among the four springsnail species.
Differences ranged from 0.0 to 0.8 percent (0 to 5 base pairs) among
the four springsnail species and 2.6 to 6.9 percent (16 to 43 base
pairs) with congeners. Nuclear DNA data revealed differences in the
ITS-1 sequences within the four springsnail species that were
substantially smaller (0.0 to 0.6 percent) than differences among other
congeners (5.9 to 20.4 percent) (see Figure 8 in Hershler and Liu 2004,
pp. 73-75). These two lines of evidence show that DNA sequence
differences among the four springsnail species are very small compared
to differences with other recognized taxa within the genus Pyrgulopsis.
Hershler and Liu (2004, p. 77) concluded ``three independent data
sets (morphology, mitochondrial, and nuclear DNA sequences) congruently
suggest that these four Natricola snails do not merit recognition as
distinct species according to various currently applied concepts of
this taxonomic rank.'' The methods employed by Hershler and Liu (2004,
pp. 67-70) are considered contemporary in the field of genetics and are
consistent with those used by numerous authors reconstructing
phylogenies based on molecular evidence in general (Raahauge and
Kristensen 2000, pp. 87-89; Jones et al. 2001, pp. 281; Attwood et al.
2003, pp. 265-266), and with western hydrobiid snails in particular
(Hershler et al. 2003, pp. 358-359; Liu et al. 2003, pp. 2772-2775;
Hurt 2004, pp. 1174-1177; Liu and Hershler 2005, p. 285). Further, it
is the position of the American Malacological Society that the Hershler
and Liu (2004) revised taxonomy sets the standard for understanding
this group of springsnails (Leal 2004). Hershler and Liu (2004, pp. 66-
81) represents the best available scientific and commercial data on the
taxonomic status of the four petitioned springsnails, and we therefore
will refer to the four former springsnail species as Pyrgulopsis
robusta for the rest of this document.
Biology
Pyrgulopsis robusta shells are large for the genus, usually ovate
(oval) to narrow-conic (cone shaped), rarely subglobose (not quite
rounded), with whorls weakly to moderately convex (curving outward).
The shell is clear-white and the periostracum (outer layer of the shell
matrix) is tan. The aperture is ovate and weakly angled above. The
inner lip is complete in larger specimens. The penial lobe and filament
are about equal in length. The dorsal proximal lobule is well
developed, usually overlapping the base of the filament and often borne
on a weak proximal swelling. The terminal gland is elongate and
transverse. The dorsal distal lobule is well developed and is usually
bearing one or a series of small glands. The ventral lobule is well
developed and bears a large gland (Hershler and Liu 2004, p. 79).
Information available to describe the life history of Pyrgulopsis
robusta varies widely. The species is hypothesized to primarily feed on
periphyton (i.e., diatoms and algae), which covers the surface of most
benthic (submerged bottom) substrates. Although little specific
information exists regarding reproductive strategies of P. robusta,
members of the genus Pyrgulopsis are generally dioecious (i.e., male
and female individuals) (Dillon 2000, pp. 102-103; Lysne 2003, p. 80).
Pyrgulopsis robusta is hypothesized to
[[Page 56941]]
reproduce once in an annual life cycle, and laboratory studies estimate
average survival to be 382 days (Lysne 2003, p. 82). However, field
data show that not all P. robusta die within a year (Finni 2003a, pp.
3-5), a life history pattern suggested by Dillon (2000, p. 162) to be
exhibited by many populations, allowing extended survivorship and
multiple reproductive events. Additional P. robusta life history
information regarding reproduction and growth rates can be found in the
following references: Finni 2003a, pp. 3-5; Lysne 2003, pp. 24, 36, 38,
79-81; Riley et al. 2003, p. 33; Dillon 2000, p. 103; and, Hershler
1994, pp. 1-119.
Habitat
Species in the genus Pyrgulopsis require permanent fresh waters
(Taylor 1985, pp. 265, 276; Hershler 1998, p. 1; Hershler and Sada
2002, p. 255). Pyrgulopsis robusta utilizes a wide range of flow
conditions and habitats. For example, P. robusta has been found in the
mainstem Snake River, Idaho, in various habitats; in C.J. Strike and
Swan Falls Reservoirs, Idaho (Clark 2005); and in two springs that flow
through Yellowstone National Park and John D. Rockefeller National
Parkway in Wyoming: Marmot Spring, a relatively stable groundwater-fed
spring, and Polecat Creek, a geothermal spring (Riley 2005a, pp. 1, 8;
Hall et al. 2003, p. 408). In southeastern Oregon, P. robusta primarily
occurs in cold springs and spring pools of variable size (Frest and
Johannes 1995, p. 196), but is also found in the South Fork Malheur
River (Hershler and Liu 2004, p. 67). Although P. robusta evolved in
prehistoric Lake Idaho (Taylor 1982, p. 2; Taylor 1985, pp. 288, 309),
the species presently occurs more frequently and abundantly in river
habitat than in lake or reservoir habitat (Clark 2005).
Pyrgulopsis robusta is found on a wide range of substrates in the
Snake and Columbia Rivers, from silt and pebbles to cobbles and
boulders, but in the Snake River the species achieves highest density
on gravel to cobble substrates (Stephenson et al. 2004, A3 pp. 1-4, A4
pp. 1-4). In Southeastern Oregon, the species is generally found on
coarse sand to cobble substrates but may also be associated with the
submerged aquatic plant genus Rorippa (Frest and Johannes 1995, p.
196).
Field and laboratory information indicate Pyrgulopsis robusta has a
wide temperature tolerance (Stephenson and Bean 2003, pp. A1, A2;
Stephenson et al. 2004, A3 pp. 1-4, A4 pp. 1-4; Lysne 2003, p. 27).
Pyrgulopsis robusta has been documented to survive and grow at
temperatures that exceeded the State of Idaho's water temperature
criteria for cold-water life of 66 degrees Fahrenheit (F) (19 degrees
Celsius (C)) mean daily and 72 degrees F (22 degrees C) maximum daily
water temperatures (Lysne 2003, pp. 27-29). Pyrgulopsis robusta have
been routinely collected in the Snake River at water temperatures
greater than 68 degrees F (20 degrees C) (Stephenson and Bean 2003, pp.
A1, A2; Stephenson et al. 2004, A3 pp. 1-4, A4 pp. 1-4). In Wyoming,
high numbers of P. robusta have been collected in Polecat Creek, a
geothermal spring creek with temperatures ranging from approximately
57.2 degrees F (14 degrees C) in winter to 75.2 degrees F (24 degrees
C) in summer (Hall et al. 2003, p. 408). Other variables that
potentially influence P. robusta habitat selection and use have not
been well documented.
Range and Distribution
Pyrgulopsis robusta is now comprised of four geographically
isolated populations that include the northwestern Wyoming population,
the Snake River population in Idaho, the Columbia River population in
Oregon and Washington, and the Oregon closed-basin population (Hershler
1994, p. 91; Hershler 1998, p. 99; Riley et al. 2003, p. 6; Frest
2005a; Riley 2005b). In Wyoming, P. robusta is currently known from
only two locations in Yellowstone National Park and John D. Rockefeller
National Parkway. There have been past collections at other sites, and
P. robusta may be found at additional locations in the future. Recent
surveys have failed to locate the species in Jackson Lake (Riley
2005b), the type locality of P. robusta as described by Walker in 1908.
In southeastern Oregon, Pyrgulopsis robusta occurs in few locations
(six or fewer) in the Oregon Interior Basin, in isolated cold springs
and spring pools (Frest and Johannes 1995, p. 196), and in the South
Fork Malheur River, a tributary to the Snake River (Hershler and Liu
2004, p. 67), in Harney and Lake Counties. Pyrgulopsis robusta was
historically found along the shores of Malheur and Harney Lakes (Frest
and Johannes 1995, p. 196) and was associated with open water habitats
(as opposed to wetland habitats with emergent vegetation) 8,000 to
10,000 years ago (Wriston 2003, p. 28). Pyrgulopsis robusta is not
known to currently exist in Harney or Malheur Lakes, and it is
uncertain when P. robusta last existed there (Frest and Johannes 1995,
p. 196). Many isolated springs and other aquatic habitats of Utah,
Nevada, and Idaho in the Great Basin, including parts of southeastern
Oregon, have been surveyed specifically for springsnails, but no
additional P. robusta have been located (Hershler 1998, p. 3; Hershler
and Sada 2002, p. 259).
In the Snake River, Pyrgulopsis robusta is known to occur at
numerous locations along a stretch of 214 river miles (344 kilometer
(km)) between river mile (rm) 340 (river kilometer mile (rkm) 547) and
rm 554 (rkm 892). There have been at least 174 collections from this
reach of river and the extent of P. robusta is believed to be well
defined and relatively abundant. The distribution of P. robusta in the
Columbia River is less well known than in the Snake River, particularly
in the Hanford Reach below Priest Rapids Dam. In the Columbia River, P.
robusta is known from 17 locations, beginning at approximately rm 20
(rkm 32) and continuing for nearly 400 miles (649 km) upstream to just
below Priest Rapids Dam (Frest 2005a). Although there have been several
hundred invertebrate samples collected in the Columbia River over the
past several years, P. robusta has been found only in a few of these
samples (Frest 2005a).
Status Review Process
On April 20, 2005, we initiated combined 12-month status reviews
(70 FR 20512) of the petitioned springsnails, as well as a 5-year
review of the Idaho springsnail under section 4(c)(2)(A) of the Act,
and solicited additional information from the public on the biology,
ecology, distribution and status, threats affecting the petitioned
springsnail species, and any ongoing or planned conservation measures.
During the 60-day public comment period, we contacted numerous
Federal and State resource agencies, interested Tribal governments, and
County governments. On June 7, 2005, we attended an information
exchange meeting with the State of Idaho Office of Species
Conservation, Idaho Department of Fish and Game (IDFG), Idaho
Department of Environmental Quality (IDEQ), U.S. Bureau of Reclamation
(BOR), U.S. Bureau of Land Management (BLM), and others. After this
information exchange meeting, our staff assimilated and analyzed all
the new information submitted during the 60-day public comment period,
along with the existing information already obtained from published
scientific literature, unpublished technical documents, and written and
personal communications. As part of our routine Status Review process,
we took this synthesized information and created a document titled:
Draft Best Available Biological Information for Four Petitioned
Springsnail Species from
[[Page 56942]]
Idaho, Oregon, Washington, and Wyoming (Draft BAI). The Draft BAI
represented our comprehensive, best available scientific and commercial
information on the petitioned springsnails.
On August 3, 2005, through a widely distributed outreach effort
that included a news release, Dear Interested Party letter, posting on
the Service's Web site, and a request for peer review, we opened an
additional 30-day public and peer review comment period on the Draft
BAI. After the public and peer review, Service staff incorporated the
additional information and technical corrections received, and wrote
Version 2.0 Best Available Biological Information for Four Petitioned
Springsnail Species from Idaho, Oregon, Washington, and Wyoming (BAI).
The revised BAI constituted the peer-reviewed state of knowledge with
regard to the taxonomy, biology, ecology, distribution, and status of
the four petitioned springsnail species, now combined as Pyrgulopsis
robusta, and was used throughout the remainder of the Status Review
process as the primary source of best available scientific and
commercial data.
The Service utilized a structured decision making model to assess
the available data. Based on an early assessment of the degree of
uncertainty surrounding the population trends and conservation status
of Pyrgulopsis robusta, the Service used two panels to inform our
recommended course. The first panel (Expert Panel) was made up of six
scientists from outside the Service with expertise in relevant fields,
including snail biology and ecology, community ecology, population
ecology, stream ecology, aquatic ecotoxicology, and regional water
quality. This Expert Panel met on October 18-19, 2005, to discuss the
strengths and weaknesses of the various data, hypotheses, and opinions
relative to the current status of P. robusta. The Expert Panel only
addressed the scientific aspects of risk and threats, and estimated the
probable extinction risk to P. robusta. A second ``Managers Panel'' of
five Service managers and senior biologists met on October 20-21, 2005,
to consider the Expert Panel's input and all other information
necessary to conduct an extinction risk assessment of P. robusta.
Information generated from these two Panels was used in the Service's
status review to assess threats to, and evaluate the listing status of,
P. robusta. Further details about the structured decision making
process used by the two panels are documented in our administrative
record for this proposed rule.
Inspection of the petition to delist the Idaho springsnail, the
petition to list the Jackson Lake, Harney Lake, and Columbia
springsnails, and the supporting information, administrative finding,
and other relevant materials may be made in person, by appointment, at
the address listed above (see ADDRESSES).
Summary of Factors Affecting the Species
Section 4 of the Act and regulations (50 CFR Part 424) promulgated
to implement the listing provisions of the Act set forth the procedures
for listing, reclassifying, and delisting species. A species may be
listed as threatened or endangered if one or more of the five factors
described in section 4(a)(1) of the Act threaten the continued
existence of the species. A species may be delisted, according to 50
CFR 424.11(d), if the best scientific and commercial data available
substantiate that the species is neither endangered nor threatened
because of: (1) Extinction; (2) recovery; or (3) error in the original
data, or the data analysis, used for classification of the species. For
species that are being considered for delisting, the analysis of
threats must include an evaluation of threats that existed at the time
of listing and those that currently exist or that could, with a
reasonable degree of likelihood, potentially affect the species in the
foreseeable future after its delisting and the consequent removal of
the Act's protections.
A. The Present or Threatened Destruction, Modification, or Curtailment
of Its Habitat or Range
The 1992 final listing rule (57 FR 59244) described activities such
as proposed large hydroelectric dam developments, peak-loading
operations of existing hydroelectric water projects, small
hydroelectric developments, water pollution, and water diversions whose
cumulative effects threatened the habitat and fragmented populations of
the Idaho springsnail (Pyrgulopsis idahoensis). After reviewing the
best available scientific and commercial information regarding present
or threatened destruction, modification, or curtailment of the habitat
or range of P. robusta, we determined that the principal habitat-
related threats are not proceeding at a rate that will threaten the
continued existence of the species within the foreseeable future.
Dams and Reservoirs
Our 1992 listing of the Idaho springsnail was based on information
that indicated that the species was found only in permanent flowing
waters of the mainstem Snake River, and that its historic range had
been reduced nearly 80 percent, in large part by dam and reservoir
development and operations.
Populations of Pyrgulopsis robusta have been collected from various
habitats, including springs, river reaches, and both lake and reservoir
locations (Bickell 1977, p. 33; Hershler 1998, p. 99; Richards and
Lester 2002, pp. 6-7; Stephenson et al. 2004, pp. 11, 21). In the Snake
River in Idaho, where P. robusta occurs over a range of 214 river miles
(344 km), the greatest number of live collections and the highest
percentages of P. robusta occurrence are generally found in flowing
waters influenced by reservoirs (Clark 2005). While extensive surveys
conducted in downstream reaches (i.e., below Hells Canyon) of the Snake
River (Shinn et al. 2001, pp. 80-82; Finni 2003b, p. 1; Richards et al.
2005, pp. 4-5) and Columbia River basins (Frest and Johannes 1995, p.
203) have not documented the presence of springsnails, springsnails
have been known to persist in habitats associated with reservoirs
(i.e., C.J. Strike and Swan Falls). At the upstream end of their range
in C.J. Strike Reservoir, abundant numbers of springsnails are located
at the mouth of a small tributary (i.e., main-pool) and on the gravel
shores of the Bruneau River Arm, where comparatively cool and flowing
waters (i.e., relative to the Snake River) of the Bruneau River run
into C.J. Strike Reservoir (Stephenson et al. 2004, p. 21). In Swan
Falls Reservoir, P. robusta are found in the headwaters (i.e., the
nebulous upstream end of a reservoir and downstream end of free-flowing
river) of the reservoir, but only one snail has been collected (at rm
460; rkm 740) in the main pool from the dam to 7 miles (11.2 km)
upstream of the dam (Clark 2005).
At the downstream end of Pyrgulopsis robusta's range in Idaho, the
species' known distribution ends immediately above the Hells Canyon
Complex at the headwaters of Brownlee Reservoir (approximately rm 340
(rkm 547)). The Hells Canyon Complex includes three large reservoirs
(Brownlee, Oxbow, and Hells Canyon) that are deep (two have very steep
sides) and whose waters fluctuate on both a daily and annual basis
(Esch 2005). Surveys by the IPC in and below the Hells Canyon Complex
have not yielded P. robusta (Finni 2003b, pp. 9, 19; Meyers and Foster
2003, pp. 17-18; Richards et al. 2005, pp. 71-78, 103-149). The
particular habitat conditions of these reservoirs may not be able to
support P. robusta and may also prevent successful
[[Page 56943]]
downstream migration to suitable habitat below the Hells Canyon Complex
(Shinn et al., 2001, p. 20; Meyers and Foster 2003, pp. 18-20).
In Oregon and Washington, Pyrgulopsis robusta has been documented
in the lower Columbia River below Dalles and John Day Dams and in their
pools (Frest 2005a). These collections were in areas where the flow is
greater and the river is shallower than in the reservoir (Frest 2005a).
In southeastern Oregon, P. robusta was found in the south fork of the
Malheur River (Hershler and Liu 2004, p. 79; Frest 2005a). These
collections were reported to have been taken 60 miles upstream of Warm
Springs Dam in an area of spring up-welling from the hyporheic zone
(area below the streambed where water passes through spaces between the
rock and cobble) (Frest 2005a, b).
Our current status review indicates that Pyrgulopsis robusta is not
restricted to permanent free-flowing water; the species also occurs in
slower moving reservoir reaches and also in areas with and without
spring inflow or upwelling occurrences. Our previous concern, as stated
in the 1992 listing rule, regarding the historic range of the species
in the Snake River having been reduced nearly 80 percent by dams and
reservoirs, does not apply to P. robusta. New information collected on
the Idaho springsnail population's life history, distribution, and
status has been incorporated into this status review, together with
information about the three other P. robusta populations (Jackson Lake,
Harney Lake, and Columbia River). Much of this information has been
collected during aquatic and mollusk surveys conducted by the IPC in
the Snake River and Frest (2005 a, b) for the Columbia River and
southeast Oregon populations. The IPC has been collecting information
on Idaho springsnail populations throughout the Snake River since 1995.
Based on the results of these surveys and laboratory studies, we now
have a much better understanding of the basic life history as well as
current distribution and status of P. robusta in the Snake River. These
surveys have documented that P. robusta is more widely distributed in
the Snake River than originally described in the 1992 listing rule. IPC
biologists have surveyed over 400 river miles (644 km) in the Snake
River and have documented the species at over 174 known locations over
214 river miles (344 km), between rm 340 (rkm 547) and rm 554 (rkm 892)
(Clark 2005), a nearly 500 percent increase, or 179 river miles (292
km), of its known range. In summary, P. robusta has been determined to
be more widely distributed and to occur on a much wider diversity of
substrate types and sizes, and in a greater variety of aquatic habitats
than was known at the time of the Idaho springsnail's listing in 1992.
The species occurs throughout long reaches of the Snake River and
Columbia Rivers in areas that are influenced by dams and reservoirs.
The 1992 listing rule discussed ``peak-loading, the practice of
artificially raising and lowering river levels to meet short-term
electrical needs by local run-of-the-river hydroelectric projects,'' as
a threat that ``may adversely affect three known populations of the
Idaho springsnail'' (57 FR 59252). Certain hydroelectric power
generating operational scenarios (e.g., water storage, diversion, and
peak-loading) have been documented to have adverse impacts on aquatic
communities (Armitage 1984, pp. 141-143; Brusven 1984, p. 167; Vaughn
and Taylor 1999, pp. 915-916; Watters 2000, p. 1). C.J. Strike Dam is
the primary peak-loading hydroelectric facility in the Snake River, yet
Pyrgulopsis robusta persists in the peak-loading-affected area (Clark
2005). For example, the largest monitored colony of P. robusta exists
in the Snake River approximately 3 river miles (4.8 km) downstream of
C.J. Strike Dam (Stephenson et al. 2004, p. 14). The Expert Panel and
Service's Manager Panel both acknowledged that because colonies of P.
robusta are widespread and known to occur over a 214-mile (344-km)
stretch of the Snake River that is subject to long-term, recurring
peak-loading and fluctuating flows, these colonies are resilient and
will likely continue to persist into the foreseeable future.
The effects of dams and reservoirs have been suggested as barriers
to dispersal for Pyrgulopsis robusta. Species that have limited
distributions and/or smaller, isolated populations may have a higher
risk of local extirpations due to various threats and demographic
stochasticity (variability) (Meffe et al. 1997, pp. 284-299; Vaughn and
Taylor 1999, p. 916; Fagan et al. 2002, p. 3250). Both the Expert
Panelists and Service's Manager Panelists acknowledged this risk for
springsnails, but did not expect these populations to become extirpated
due to possible barriers to dispersal in the foreseeable future.
Groundwater Pumping
Groundwater pumping is only a concern for Pyrgulopsis robusta
populations in southeast Oregon. Groundwater pumping for domestic use,
agriculture, and industry may deplete flows from groundwater-fed spring
systems by altering, modifying, or curtailing habitats dependent on
those groundwater sources (Sada and Vinyard 2002, pp. 277-278).
The Oregon Water Resources Department (OWRD) regulates water
development (OWRD 2005a), but very little information is available for
the Malheur Basin or the Abert Lake Basin, where the Harney Lake
population of Pyrgulopsis robusta is found. While spring development
and/or destruction have been implicated in native species declines in
southeastern Oregon (Frest and Johannes 1995, p. 196), we are not aware
of spring alterations, modifications, or conservation efforts that are
affecting P. robusta in southeastern Oregon. Although at least one
location previously containing P. robusta in southeastern Oregon no
longer has springsnails (Hershler 1994, p. 41; Frest and Johannes 1995,
p. 196), groundwater pumping can not be explicitly linked to the
springsnail's absence. In two OWRD observation wells in the Malheur
Basin, groundwater levels seem to have been relatively stable since
1960 (OWRD 2005b). We acknowledge that diversion of springwater flows
and groundwater pumping can represent barriers to dispersal and
potentially isolate populations of P. robusta. However, these effects
are limited to populations only in southeast Oregon, and not elsewhere
in the species' range.
Water Quality--Temperature, Nutrients, and Chemical Stressors
The 1992 listing rule (57 FR 59244) stated, ``The quality of water
in these habitats has a direct effect on the species survival. The
species requires cold, well-oxygenated unpolluted water for survival.
Any factor that leads to a deterioration in water quality would likely
extirpate these taxa.''
Numerous reaches of the Snake and Columbia Rivers are classified as
water-quality-impaired due to the presence of one or more pollutants
(e.g., total phosphorous, sediments, total coliforms) in excess of
State or Federal guidelines. Nutrient-enriched waters primarily enter
the Snake and Columbia Rivers via springs, tributaries, fish farm
effluents, municipal waste treatment facilities, and irrigation returns
(U.S. Environmental Protection Agency (USEPA) 2002, pp. 4-20 to 4-22;
USFWS 2004, p. 1; U.S. Geological Survey (USGS) 2005, p. 5). Irrigation
water returned to rivers is generally warmer, contains pesticides or
pesticide byproducts, has been enriched with nutrients from agriculture
(e.g., nitrogen
[[Page 56944]]
and phosphorous), and frequently contains elevated sediment loads.
Pollutants in fish farm effluent include nutrients derived from
metabolic wastes of the fish and unconsumed fish food, disinfectants,
bacteria, and residual quantities of drugs used to control disease
outbreaks. Recent research found elevated levels of fine sediments and
nitrogen as well as elevated levels of trace elements, including zinc,
copper, cadmium, lead, and chromium, immediately downstream of
aquaculture discharges (Falter and Hinson 2003, p. 53). Additionally,
concentrations of lead, cadmium, and arsenic were detected in snails
collected during a research study in the Snake River (Richards 2002).
Researchers at the USGS (1998, p. 15) detected concentrations of some
pesticides in fish tissues, streams, irrigation canals, and irrigation
returns in the Snake River Basin in concentrations exceeding the
aquatic-life criteria established by the USEPA. While some effects of
pollutants, including metals and organic compounds in stream organisms,
are documented in the literature (Naimo 1995, pp. 351-352; Clements
1999, pp. 1076-1078; Courtney and Clements 2002, pp. 1770-1773), the
potential impact of these contaminants on Pyrgulopsis robusta has not
been studied and is unknown. However, P. robusta has been documented to
occur downstream in these stretches of the Snake River where municipal,
aquaculture, and agricultural discharges occur.
In the upper Snake River Basin in Wyoming, very low levels of
ammonia, nitrite and nitrate, phosphorus, trace metals, and pesticides
have been detected in water quality assessments (USGS 2004, p. 39).
Polecat Creek, which contains Pyrgulopsis robusta (Riley et al. 2003,
p. 6), was included in Wyoming's section 303(d) of the Clean Water Act
list of impaired waterbodies due to fecal coliform contamination (WDEQ
2004, pp. 1-91). However, water quality in the upper Snake River Basin
in Wyoming is generally described as good (USGS 2004, p. 38).
Changes in a river's flow and depth as a result of dams lead to
changes in sediment deposition dynamics and thermal characteristics
(Poff et al. 1997, p. 773; Platts 1992, p. 2). Water-transported
sediments that would be flushed downstream and deposited in pools,
eddies, and other still water environments under normal river flows now
settle in slow moving reservoir waters (Poff et al. 1997, p. 773;
Simons 1979, pp. 96, 100-104). Additionally, drops in water velocity in
reservoirs may result in elevated surface water temperatures and
reductions in dissolved oxygen (USGS 2005, p. 11). Pyrgulopsis robusta
has adapted to, and survives in, a relatively wide range of
temperatures within the Snake River (Lysne 2003, p. 27). The IPC has
collected P. robusta in water temperatures ranging from near freezing
to 80 degrees F (27 degrees C) (Clark 2005). While high temperatures
may be of concern for some aquatic snail species, we are not aware that
water temperature limits growth, reproduction, or survival of P.
robusta in any portion of its range. Pyrgulopsis robusta is widespread
and abundant, occurring in a variety of water quality, flow, and
temperature ranges. Expert and Manager Panels noted that water quality
has not significantly modified or curtailed the habitat or range of P.
robusta to an extent that threatens the continued existence of the
species.
Grazing
Grazing by cattle has been suggested to be a threat to Pyrgulopsis
robusta habitat in southeastern Oregon (Frest and Johannes 1995, p.
196), but not in other areas. However, little information exists
regarding the impact of livestock grazing on the P. robusta in
southeastern Oregon. Since the mid 1980s, cattle have been excluded
from riparian areas, springs, and spring creeks in both the Harney and
Malheur Lakes region (Burnside 2004). The Expert and Manager panels
agreed that grazing does not appear to constitute a threat to the
continued existence of the species since it is limited only to portions
of the southeastern Oregon populations.
Summary of Factor A
In summary, Pyrgulopsis robusta is distributed over a wide
geographic area and a wide range of aquatic habitats in Idaho, Oregon,
Washington, and Wyoming. Based on new information, previous concerns
about the species being restricted to permanent free flowing water and
a reduction in range limiting its distribution or threatening its
existence are no longer valid. For example, since the 1992 listing, P.
robusta in the Snake River has been collected at 174 locations over 214
river miles (342 km). We are not aware that water temperature limits
growth, reproduction, or survival of P. robusta in any portion of its
range. Dam-induced changes to large river habitats in the Snake River
or Columbia River may create conditions that likely represent barriers
to P. robusta migration; however, the species persists throughout long
reaches of these two river systems in areas influenced by dams and
hydroelectric operations. Barriers to dispersal (i.e., isolated and
fragmented populations) were considered a threat factor by the Expert
Panel for the southeastern Oregon populations, but were considered
relatively insignificant in both the Snake and Columbia Rivers. The
fact that P. robusta is often locally abundant, resilient, and
adaptable to a range of extrinsic factors, contributes to the
determination that P. robusta is not in danger of extinction within the
foreseeable future. Thus, based on the best scientific and commercial
data, we conclude that the present or threatened destruction,
modification, or curtailment of P. robusta's habitat or range is not a
factor that threatens or endangers the species throughout all or a
significant portion of its range.
B. Overutilization for Commercial, Recreational, Scientific, or
Educational Purposes
Overutilization of Pyrgulopsis robusta for commercial,
recreational, or scientific purposes was not considered to be an
applicable threat at the time of the 1992 listing (57 FR 59242), and is
still not considered by the Expert Panel and Service's Manager Panel to
be a threat to P. robusta throughout all or a significant portion of
its range.
C. Disease or Predation
We have no information on the actual effects of disease or
parasites on Pyrgulopsis robusta.
At the time of the 1992 listing, fish predation was not considered
to be a major threat (57 FR 59242). There is currently no information
regarding the threat of predation on the continued existence of
Pyrgulopsis robusta. Predation on snails, in general, is documented and
is a natural occurrence (Merrick et al. 1992, p. 231; McCarthy and
Fisher 2000, p. 387), but information on the effects of predation on P.
robusta is limited. In the only known account of predation by fish on
P. robusta, Beetle (1957, p. 17) reported shells were found in the
digestive tract of a Roseyside sucker (Catostomus fecundus) near
Jackson Lake Dam, Wyoming. A recent study of predation ecology with
Pyrgulopsis species failed to observe predation by native crayfish
(Pacifasticus spp.) (Lysne and Koetsier 2001, p. 6).
The Expert Panel did not identify disease or predation as a
significant threat, but information is lacking to draw any definitive
conclusions about risks to Pyrgulopsis robusta due to predation. Based
on the best scientific and commercial data available, we conclude that
disease and predation are
[[Page 56945]]
not factors that endanger or threaten P. robusta throughout all or a
significant portion of its range.
D. The Inadequacy of Existing Regulatory Mechanisms
In the 1992 Idaho springsnail listing rule (57 FR 59244), nutrient
loading and pollution in the middle Snake River were identified as
areas of concern. We stated that it was unlikely that the downward
trend in water quality would be reversed any time soon, because it
would take several years before any recommendations to improve water
quality, as outlined in comprehensive resource management plans for the
Snake River, were fully implemented through local, State, and Federal
programs and efforts. However, since the 1992 listing rule, some water
quality improvements have been realized in localized reaches of the
Snake River, primarily with regard to sediment and phosphorus reduction
(Buhidar 2005). These improvements are more fully discussed in the
Water Quality Management section below.
Based on our status review, we describe various regulatory
mechanisms implemented by State and Federal resource agencies to
protect Pyrgulopsis robusta and its habitat. Federal agency regulations
are generally consistent across States, but State regulations may
differ considerably with regard to similar natural resource issues.
Analogous State natural resource agencies exist in Idaho, Oregon,
Washington, and Wyoming.
Wildlife Conservation Statutes and Plans
Washington has the comprehensive statutory authority and mandate to
``preserve and protect'' all wildlife, including invertebrates such as
Pyrgulopsis robusta, within its borders (Revised Code of Washington
77.04.012). The Idaho Department of Fish and Game (IDFG) developed a
Comprehensive Wildlife Conservation Strategy (Idaho Strategy) that
lists P. robusta as a ``species of greatest conservation need'' (IDFG
2005, p. 413). For example, Pyrgulopsis robusta conservation will be
considered when IDFG engages other States, Federal agencies, and other
conservation partners on proposed activities affecting Snake River
habitats (e.g., boat ramp construction). The Idaho Natural Heritage
Program lists Idaho springsnail as a species of concern, the Oregon
Natural Heritage Program lists Columbia and Harney Lake springsnails as
species of concern (ODFW 2005, p. 354), and in Wyoming, the Jackson
Lake springsnail is also listed as a species of concern (WGFD 2005, p.
15). These State wildlife conservation strategies and plans are useful
to land managers because they provide the best available information
for species of greatest conservation need and allow these managers to
make informed decisions about land use changes.
Water Quality Management
There are various State-managed water quality programs within the
range of Pyrgulopsis robusta in Idaho, Washington, Wyoming, and Oregon.
These programs are tiered off of the Clean Water Act (CWA), which
requires States to establish water quality standards that provide for
the protection and propagation of fish, shellfish, and wildlife, and
recreation in and on the water (``fishable/swimmable''). In addition,
as part of the CWA, States must also include an antidegradation policy
that protects waterbody uses, and high-quality waters. In Idaho,
Washington, Wyoming, and Oregon, point source discharges are regulated
through the National Pollutant Discharge Elimination System (NPDES)
program. These NPDES permits are written to meet all applicable water
quality standards established for a waterbody to protect human health
and aquatic life.
Idaho has established water quality standards (e.g., water
temperature and dissolved oxygen) for the protections of cold-water
biota (e.g., invertebrate species) in many reaches of the Snake River.
Although conditions within the river periodically exceed these limits
during the summer months (USGS 2005, pp. 7-12), Pyrgulopsis robusta has
been collected in water temperatures ranging from near freezing to 80
degrees F (27 degrees C) (Clark 2005). While high temperatures may be
of concern for some aquatic snail species, water temperature does not
seem to limit growth, reproduction, or survival of P. robusta in any
portion of its range.
Waters that do not meet standards due to point- and non-point
source pollution are listed on USEPA's 303(d) list of impaired water
bodies. States must submit to USEPA a 303(d) list (water quality-
limited waters) and a 305(b) report (status of the State's waters)
every two years. Water quality improvements with regard to point and
non-point sources have been realized in localized reaches of the Snake
River where P. robusta occurs (Buhidar 2005), primarily with regard to
sediment and phosphorus criteria. The IDEQ, under authority of the
State Nutrient Management Act, is coordinating efforts to identify and
quantify contributing sources of pollutants (including nutrient and
sediment loading) to the Snake River basin via the Total Maximum Daily
Load (TMDL) approach. TMDLs are developed, adopted, and implemented
within State Agricultural Water Quality Program, CWA section 401
Certification, BLM Resource Management Plans, the State Water Plan, and
local ordinances.
In Oregon, point- and non-point source pollution is managed by
Oregon's Department of Environmental Quality (ODEQ). TMDLs for several
stream reaches are in development for the Malheur River Basin where
Pyrgulopsis robusta exists. TMDLs establish mechanisms to address point
and non-point sources to bring these reaches into compliance with water
quality standards.
In Washington, the State's Department of Ecology (WECY) has a
mandate to manage point and non-point sources of pollution entering
Washington's waters (WECY 2005). Non-point sources of pollution are
regulated by numerous State of Washington statutes (WECY 2005), and
managed primarily through Washington's Water Quality Management Plan to
Control Non-point Source Pollution (Plan), published in 2000.
Pyrgulopsis robusta is found in the Columbia River, and the Plan may
indirectly benefit the springsnails that occur there.
In Wyoming, Pyrgulopsis robusta exists within waters that occur in
National Parks and are designated as Class 1 or ``outstanding waters''
by the Wyoming Department of Environmental Quality. Maintaining this
designation is one of the National Park Service's highest priorities
(USGS 2004, p. 2). We are not aware of any proposals to modify these
designations or of activities that would impair these water bodies.
Federal Land Management
Many large scale Federal management plans (e.g., U.S. Forest
Service Land and Resource Management Plans, U.S. Bureau of Land
Management (BLM) Resource Management Plans, National Wildlife Refuge
Comprehensive Conservation Plans, and Interior Columbia Basin Ecosystem
Management Plan) promote conservation of aquatic and terrestrial
habitats, including those on which Pyrgulopsis robusta depends.
Much of the Federal lands adjacent to the Snake River in Wyoming,
Idaho, Oregon, and Washington are managed by the BLM. Resource
Management Plans (RMPs) that guide BLM resource management include
provisions to protect water quality and riparian habitats. The Service
and the BLM in Idaho have finalized a Conservation
[[Page 56946]]
Agreement (USBLM 2006, pp. 1-11) that commits the BLM to carry out
specific actions to assess status and distribution of P. robusta in
areas affected by management actions and also to modify those actions
to avoid and minimize impacts to the species in the Snake River. In
addition, BLM has completed Endangered Species Act section 7
consultations for some actions that may affect P. idahoensis, now known
as P. robusta. The BLM's Boise and Twin Falls Districts have completed
a joint section 7 consultation for ongoing livestock grazing activities
in allotments adjacent to P. robusta habitats in the Snake River. Under
that consultation, the BLM and grazing permitees have implemented
actions to reduce the amount of shoreline grazing and grazing-related
sediment, thereby reducing the risk of take of P. robusta resulting
from livestock management.
Water Rights and Operations
In Idaho, there have been improvements in Snake River water
management since the time of listing the Idaho springsnail in 1992 (57
FR 59244). Portions of the Snake River are temporarily protected from
further allocation of consumptive use water rights (Barker et al. 2005)
by order of the Director of the Idaho Department of Water Resources,
although this does not preclude future water diversion or consumption
projects within the range of Pyrgulopsis robusta in the Snake River of
Idaho. For the other geographic areas where P. robusta occurs, we are
not aware of any State-sponsored programs restricting allocation of
consumptive use water rights.
The U.S. Bureau of Reclamation (BOR) operates numerous water
projects in the Snake River basin and is involved in a variety of fish
and wildlife conservation efforts through a number of different
programs in Oregon, Washington, and Idaho (USBOR 2005). The BOR has
conducted numerous surveys for sensitive mollusks for several years
(USBOR 2002, p. 2; 2003, p. 2; 2004, p. 2). Pyrgulopsis robusta has not
been found in the upper reaches of the Snake River. The BOR has
developed 10-year Resource Management Plans designed to create a
balance of resource development, recreation, and protection of natural
and cultural resources for the lands and waters they manage. These
plans outline resource management policies and actions that will be
implemented to protect natural resources (e.g., sensitive mollusk
species) over each plan's 10-year life (USBOR 2005).
The U.S. Army Corps of Engineers (USACE) operates several
hydroelectric projects on the Columbia River within the known range of
Pyrgulopsis robusta, including John Day, Dalles, and Bonneville Dams.
Since passage of the National Environmental Policy Act of 1969,
environmental protection has been an important mission for the
Northwestern Division of the Corps (USACE 2005). Since legislation
passed in 1990 establishing environmental protection as one of the
primary missions of water resource projects, the Corps has taken steps
to ensure that projects meet Federal, State, and local environmental
requirements (USACE 2005).
A Settlement Agreement between the IPC and Service concerning the
relicensing of IPC's mid-Snake and C.J. Strike hydroelectric projects
(IPC and USFWS 2004) requires IPC to implement studies to assess
effects on two listed Snake River aquatic snails, including Pyrgulopsis
robusta, from operation of hydroelectric dams. The 1992 listing rule
stated that proposals for numerous small hydroelectric projects to be
developed on remaining free-flowing portions of the middle Snake River
within the species' range, threatened the Idaho springsnail. However,
those proposals have subsequently been withdrawn or were not approved
by the Federal Energy Regulatory Commission (FERC) (Barker et al.
2005), reducing the likelihood of new FERC licensed hydroelectric
projects impacting P. robusta.
Summary of Factor D
A wide variety of regulatory mechanisms managed by State and
Federal resource agencies are in place to manage and protect
Pyrgulopsis robusta and the habitats upon which it depends. Federal
land management plans address conservation of P. robusta habitats, and
Federal and State agencies are managing water projects to minimize
impacts on P. robusta and protect the water quality where the species
occurs. Water withdrawals for the allocation of consumptive water use
in the Snake River basin have been halted through a temporary
moratorium by the State of Idaho. Additionally, IPC hydroelectric
projects on the Snake River in Idaho have begun to address P. robusta
management needs via specific commitments in recent Settlement
Agreements. Given that P. robusta occurs as multiple populations
distributed over a wide geographic area, and a wide range and variety
of habitat types, the variety of State and Federal regulatory
mechanisms that directly and indirectly provide conservation benefits
for P. robusta are generally considered adequate.
E. Other Natural or Manmade Factors Affecting Its Continued Existence
Numerous non-native and invasive species have become established
throughout the range of Pyrgulopsis robusta, and others threaten to
become established; however, their impacts on native species and
ecosystems have not been well studied or understood. (Frest and
Johannes 2000, p. 1; Anderson 2004, pp. 15-18; Sytsma et al. 2004, pp.
33-34).
In the 1992 listing rule (57 FR 59244) for the Idaho springsnail,
we stated that the New Zealand mudsnail (Potamopyrgus antipodarum) was
a potential threat to the Idaho springsnail. The New Zealand mudsnail
was discovered in North America in 1987 in the Snake River, and has
spread rapidly (Bowler 1991, p. 175; Richards and Lester 2003, p. 1;
Richards et al. 2004, p. 114). The New Zealand mudsnail appears to
flourish in warm waterbodies in Wyoming and Montana on substrates of
silt to cobbles (Hall et al. 2003, p. 407; Cada 2004, p. 29), but is
also reported to reach high densities within the much cooler waters of
the Snake River (Clark et al. 2005, p. 17). The wide physical and
physiological tolerances of the New Zealand mudsnail allow it to thrive
in various habitats (Richards et al. 2001, pp. 375, 378; Hall et al.
2003, p. 408). The ability of the New Zealand mudsnail to occupy
numerous habitat types, including those typically occupied by native
snails (Richards et al. 2001, pp. 375, 378; Richards 2004, pp. 137-
139), does not always provide a competitive advantage for the New
Zealand mudsnail in interactions with native species (Cowie 2004).
In the Greater Yellowstone Ecosystem, researchers found evidence
that New Zealand mudsnails limit the colonization of, and may influence
the large-scale distribution of, other macroinvertebrates (Kerans et
al. 2005, p. 135). Research in Wyoming has demonstrated that New
Zealand mudsnails have reduced densities of Pyrgulopsis robusta in
Polecat Creek in Yellowstone National Park, but P. robusta and New
Zealand mudsnails continue to co-exist (Riley et al. 2003, pp. 16-18;
Gustafson 2005, pp. 7-8). The threat the New Zealand mudsnail poses to
P. robusta remains uncertain. However, the New Zealand mudsnail does
not appear to currently endanger or threaten P. robusta throughout all
or a significant portion of its range.
The Expert Panel and Service's Manager Panel identified the threat
of non-native species, including the New Zealand mudsnail, to
Pyrgulopsis robusta's survival as low. Both panels
[[Page 56947]]
identified the lack of information about non-native species
interactions with P. robusta as an area of uncertainty. However, direct
cause and effect information that non-native species are endangering or
threatening P. robusta populations does not exist.
Thus, based on the best scientific and commercial data available,
we have concluded that other natural and manmade factors do not
endanger or threaten Pyrgulopsis robusta throughout all or a
significant portion of its range.
Summary of Threats Section
Evidence collected since the Idaho springsnail was listed in 1992
as endangered (57 FR 59244) indicates Pyrgulopsis idahoensis no longer
constitutes a distinct species. The revised species, Pyrgulopsis
robusta, is a combined taxon composed of four previously regarded as
taxonomically distinct springsnails--the Idaho, Jackson Lake, Harney
Lake, and Columbia River springsnails.
Pyrgulopsis robusta populations in the Columbia and Snake Rivers
have relatively high abundance and occur as multiple populations
distributed over a wide geographic area. The Columbia River population
of P. robusta is currently known from 17 locations starting from river
mile 20 (rkm 32) and continuing for nearly 400 river miles (644 rkm)
upstream to just below Priest Rapids Dam. In the Snake River, P.
robusta is more widely distributed than originally cited in the 1992
listing rule and has been documented at over 174 known locations, over
214 river miles (344 km). The species occurs in a range of habitat
types, and is resilient to changes in flow and water quality. Extant
populations occur in various habitats, including springs, and river
reaches characterized by a wide range of flow conditions, and both
occur in lake and reservoir locations. Pyrgulopsis robusta has adapted
to, and survives in, a relatively wide range of temperatures.
Fluctuating water temperatures likely do not limit growth,
reproduction, or survival of P. robusta in any portion of its range.
Adequate existing regulatory mechanisms contributing to P. robusta
conservation include water quality regulations and FERC hydropower
Settlement Agreements. At this time P. robusta exists in multiple
populations in the States of Oregon, Washington, Idaho, and Wyoming and
is expected to persist into the future. We evaluated the best available
scientific and commercial data regarding status of and threats to the
newly described P. robusta, and determined that the species is not in
danger of extinction, nor is it likely to become endangered in the
foreseeable future throughout all or a significant portion of its
range, and therefore does not meet the definition of threatened or
endangered.
Finding
We have carefully assessed the best scientific and commercial
information available regarding the past, present, and future threats
faced by this species. We reviewed the petitions, available published
and unpublished scientific and commercial information, and information
submitted to us during the public comment period following our 90-day
petition findings. This finding reflects and incorporates information
we received during the public comment period and responds to
significant issues (i.e., incorporates appropriate information raised
in comments regarding P. robusta taxonomy, life history, distribution,
status, and threats). We also consulted with recognized springsnail
experts and Federal and St