Endangered and Threatened Wildlife and Plants; Listing Roswell springsnail, Koster's springsnail, Noel's amphipod, and Pecos assiminea as Endangered With Critical Habitat, 46304-46333 [05-15486]
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SUPPLEMENTARY INFORMATION:
DEPARTMENT OF THE INTERIOR
Fish and Wildlife Service
50 CFR Part 17
RIN 1018–AI15
Endangered and Threatened Wildlife
and Plants; Listing Roswell
springsnail, Koster’s springsnail,
Noel’s amphipod, and Pecos
assiminea as Endangered With Critical
Habitat
Fish and Wildlife Service,
Interior.
ACTION: Final rule.
AGENCY:
SUMMARY: We, the U.S. Fish and
Wildlife Service (Service), list the
Roswell springsnail (Pyrgulopsis
roswellensis), Koster’s springsnail
(Juturnia kosteri), and Noel’s amphipod
(Gammarus desperatus) as endangered
and the Pecos assiminea (Assiminea
pecos) as endangered with critical
habitat under the Endangered Species
Act of 1973, as amended (Act). These
four invertebrates occur at sinkholes,
springs, and associated spring runs and
wetland habitats. They are found at one
site in Chaves County, New Mexico, and
Pecos assiminea is also found at one site
in Pecos County, Texas, and one site in
Reeves County, Texas.
These three snails and one amphipod
have an exceedingly limited
distribution, low mobility, and
fragmented habitat. They are imperiled
by introduced species, surface and
groundwater contamination, oil and gas
extraction activities within the
supporting aquifer and watershed, local
and regional groundwater depletion,
severe drought, and direct loss of their
habitat (e.g., through burning or
removing marsh vegetation, or flooding
of habitat). This final rule will
implement the Federal protection and
recovery provisions of the Act for these
invertebrate species. We are also
designating critical habitat for the Pecos
assiminea in Texas.
DATES: This final rule is effective
September 8, 2005.
ADDRESSES: Supporting documentation
for this rulemaking is available for
public inspection, by appointment,
during normal business hours at the
U.S. Fish and Wildlife Service, New
Mexico Ecological Services Field Office,
2105 Osuna Road NE., Albuquerque,
New Mexico 87113.
FOR FURTHER INFORMATION CONTACT:
Susan MacMullin, Field Supervisor,
New Mexico Ecological Services Field
Office (telephone, 505–761–4706;
facsimile, 505–346–2542).
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Background
It is our intent to discuss only those
topics directly relevant to this final
listing determination. For more
information on the four invertebrates,
refer to the February 12, 2002, proposed
rule (67 FR 6459). However, some of
this information is discussed in our
analyses below, such as the summary of
factors affecting the species.
Springsnails
The Permian Basin of the
southwestern United States contains
one of the largest carbonate (limestone)
deposits in the world (New Mexico
Department of Game and Fish (NMDGF)
1998). Within the Permian Basin of the
Southwestern United States lies the
Roswell Basin. Located in southeastern
New Mexico, this Basin has a surface
area of around 31,080 square kilometers
(km) (12,000 square miles [mi]) and
generally begins north of Roswell, New
Mexico, and runs to the southeast of
Carlsbad, New Mexico. The Roswell
Basin contains a deep artesian aquifer
and a shallow surficial aquifer. The
action of water on soluble rocks (e.g.,
limestone and dolomite) has formed
abundant ‘‘karst’’ features such as
sinkholes, caverns, springs, and
underground streams (White et al.
1995). These hydrogeological formations
create unique settings harboring diverse
assemblages of flora and fauna. The
isolated limestone and gypsum springs,
seeps, and wetlands located in and
around Roswell, New Mexico, and
Pecos and Reeves Counties, Texas,
provide the last known habitats in the
world for several endemic species of
fish, plants, mollusks, and crustaceans.
These species include the Roswell
springsnail and Koster’s springsnail of
the freshwater snail family Hydrobiidae,
Pecos assiminea of the snail family
Assimineidae, and Noel’s amphipod
(Gammaridae). These species are
distributed in isolated, geographically
separate populations, and likely evolved
from parent species that once enjoyed a
wide distribution during wetter, cooler
climates of the Pleistocene. Such
divergence has been well-documented
for aquatic and terrestrial
macroinvertebrate groups within arid
ecosystems of western North America
(e.g., Taylor 1987; Metcalf and Smartt
1997; Bowman 1981; Cole 1985).
North American snails of the family
Hydrobiidae inhabit a great diversity of
aquatic systems from surface to cave
habitats, small springs to large rivers,
and high energy riffles to slack water
pools (Wu et al. 1997). Snails of the
family Assimineidae are typically found
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in coastal brackish waters or along
tropical and temperate seacoasts
worldwide (Taylor 1987). Inland species
of the genus Assiminea are known from
around the world, and in North America
they occur in California (Death Valley
National Monument), Utah, New
Mexico, Texas (Pecos and Reeves
´
Counties), and Mexico (Bolson de
´
Cuatro Cıenegas).
The Roswell springsnail and Koster’s
springsnail are aquatic species. These
snails have lifespans of 9 to 15 months
and reproduce several times during the
spring through fall breeding season
(Taylor 1987; Pennak 1989; Brown
1991). Snails of the family Hydrobiidae
are sexually dimorphic (there are
characteristic differences between males
and females), with females being
characteristically larger and longer-lived
than males. As with other snails in the
family, the Roswell springsnail and
Koster’s springsnail are completely
aquatic but can survive in seepage areas,
as long as flows are perennial and
within the species’ physiological
tolerance limit. These two snails occupy
spring heads and runs with variable
water temperatures (10 to 20 ° Celsius
[C] (50 to 68 ° Fahrenheit [F])) and slowto-moderate water velocities over
compact substrate ranging from deep
organic silts to gypsum sands and gravel
and compact substrate (NMDGF 1998).
Conversely, the Pecos assiminea seldom
occurs immersed in water, but prefers a
humid microhabitat created by wet mud
or beneath vegetation mats, typically
within a few centimeters (cm) (inches
(in)) of running water.
Gastropods (snails) are a class of
mollusks with a body divided into a foot
and visceral mass and a head that
usually bears eyes and tentacles. Like
most gastropods, the Roswell
springsnail, Koster’s springsnail, and
Pecos assiminea feed on algae, bacteria,
and decaying organic material (NMDGF
1988). They will also incidentally ingest
small invertebrates while grazing on
algae and detritus (dead or partially
decayed plant materials or animals).
These snails are fairly small; Koster’s
springsnail is the largest of the three
snails, and is about 4 to 4.5 millimeters
(mm) (0.16 to 0.18 in) long with a pale
tan shell that is narrowly conical with
up to 41⁄4 to 53⁄4 whorls or twists. The
Roswell springsnail is 3 to 3.5 mm (0.12
to 0.14 in) long with a narrowly conical
tan shell with up to 5 whorls. Pecos
assiminea is the smallest of the three,
with a shell length of 1.55 to 1.87 mm
(0.06 to 0.07 in) and a thin, nearly
transparent chestnut-brown shell that is
regularly conical with up to 41⁄2 strongly
incised (shouldered) whorls and a broad
oval opening. Although their shells are
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similar, the Roswell springsnail is
distinguished from Koster’s springsnail
by a dark, amber operculum (a lid
which closes the shell opening when
the animal is retracted) with white
spiral streaks, while that of Koster’s
springsnail is nearly colorless. The
genus Assiminea can be determined
from other snail genera by an almost
complete lack of tentacles, leaving the
eyes within the tips of short eye stalks
(Taylor 1987).
Taylor (1987) first described the
Roswell springsnail from a ‘‘seepage’’
along the west side of an impoundment
in Area 7 at Bitter Lake National
Wildlife Refuge (BLNWR, Refuge),
Chaves County, New Mexico. Since
then, Mehlhop (1992, 1993) has
documented the species on the BLNWR
and in March 1995 also found it in a
spring on private land (i.e., North
Spring) east of Roswell (NMDGF 1998).
In 2004, the Roswell springsnail was
determined to have been extirpated
from this private land through habitat
alteration (NMDGF 2005b). Monitoring
efforts at BLNWR (1995 to 1998) led to
the discovery of Roswell springsnail
populations in Bitter Creek, the Sago
Springs Complex, and a drainage canal
along the west shoreline of Area 6. The
Roswell springsnail is currently known
only from BLNWR with the core
population in the Sago Springs Complex
and Bitter Creek. The Sago Springs
complex is approximately 0.3 km long
(1,000 linear feet), half of which is
subterranean with flow in the upper
reaches restricted to sinkholes. Bitter
Creek is six times longer than the Sago
Springs Complex and has a total length
of 1.8 km (1.1 miles). Monthly
monitoring and ecological studies of the
Roswell springsnail initiated at BLNWR
in June 1995 are ongoing (NMDGF
2005b, 2005c).
Roswell springsnail formerly occurred
in several other springs in the Roswell
area, but these habitats have dried up
apparently due to groundwater pumping
and no longer contain the species (Cole
1981; Taylor 1983, 1987). As noted, the
Roswell springsnail historically
occurred on private land at North
Spring, but could not be found during
surveys in 2004 (NMDGF 2005b).
Pleistocene fossils of the Roswell
springsnail are known from Berrendo
Creek and the Pecos River in Chaves
County (Taylor 1987). No populations
are currently known from these areas.
Taylor (1987) first reported Koster’s
springsnail from Sago Spring at
BLNWR. Another population was
documented in 1995 at North Spring on
private land east of Roswell and a
second population was found at
BLNWR on the west side of Area 3
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during extensive surveys conducted
between 1998 and 2001 (Warrick 2005).
The species formerly occurred in several
other springs in the Roswell area, but
these habitats have since dried up due
to groundwater pumping and no longer
contain the species (Cole 1981; Taylor
1983, 1987; NMDGF 2005b). Pleistocene
fossils of Koster’s springsnail are known
from North Spring River and South
Spring Creek in Chaves County (Taylor
1987). Monthly monitoring and
ecological studies of Koster’s springsnail
initiated at BLNWR in 1995 indicate the
species is most abundant in the deep
organic substrates of Bitter Creek
(NMDGF 1998, 2005b). It also occurs at
the Sago Springs Complex, but in lower
numbers. The species has not been
found in recent times along the western
boundary of Area 3 in BLNWR (NMDGF
2005b). Koster’s springsnail has recently
been extirpated at North Spring east of
Roswell (NMDGF 2005b).
Pecos assiminea is presently known
from two sites at BLNWR, Chaves
County, New Mexico, from a large
population at Diamond Y Spring and its
associated drainage (Diamond Y Springs
Complex), Pecos County, Texas, and at
East Sandia Spring, Reeves County,
Texas. It was thought that Pecos
assiminea occurred sporadically
´
throughout the Bolson de Cuatro
´
Cınegas, Coahuila, Mexico (Taylor
1987); however, recent investigations
indicate that the population in Mexico
might be a different species (Hershler
2005). Investigations are currently
underway to determine whether the
animals found in the vicinity of
Coahuila, Mexico, are Pecos assiminea
(Hershler 2005).
Monitoring and ecological studies of
Pecos assiminea initiated at BLNWR in
1995 showed the snail to be typically
absent from substrate samples.
Populations of Pecos assiminea occur
sporadically along Bitter Creek, and a
dense population was confirmed on
moist vegetation and on muddy surfaces
within 1 cm (0.39 in) of water in 1999
in an emergent marsh plant community
around the perimeter of a sinkhole
within the Sago Springs Complex
(NMDGF 1999).
Noel’s amphipod
Noel’s amphipod, in the family
Gammaridae, is a small freshwater
crustacean. Inland amphipods are
sometimes referred to as freshwater
shrimp. Noel’s amphipod is browngreen in color with elongate, kidneyshaped eyes, and flanked with red
bands along the thoracic and abdominal
segments, often with a red dorsal stripe.
Males are slightly larger than females,
and individuals range from 8.5 to 14.8
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mm (0.33 to 0.58 in) long (Cole 1981,
1985).
Gammarids commonly inhabit
shallow, cool, well-oxygenated waters of
streams, ponds, ditches, sloughs, and
springs (Holsinger 1976; Pennak 1989).
Because they are light-sensitive, these
bottom-dwelling amphipods are active
mostly at night and feed on algae,
submergent vegetation, and decaying
organic matter (Holsinger 1976; Pennak
1989). Young amphipods depend on
microbial foods, such as algae and
bacteria, associated with aquatic plants
(Covich and Thorp 1991). Most
amphipods complete their life cycle in
one year and breed from February to
October, depending on water
temperature (Pennak 1978). Amphipods
form breeding pairs that remain
attached for 1 to 7 days at or near the
substrate while continuing to feed and
swim (Bousfield 1989). They can
produce from 15 to 50 offspring,
forming a ‘‘brood.’’ Most amphipods
produce one brood but some species
produce a series of broods during the
breeding season (Pennak 1978).
Noel’s amphipod is one of three
species of endemic amphipods of the
Pecos River Basin occurring from
Roswell, New Mexico, south to Fort
Stockton, Texas, known collectively as
the Gammarus-pecos complex (Cole
1985). Noel’s amphipod is currently
known from the following sites at
BLNWR: Sago Springs Complex, Bitter
Creek, along the western boundary of
Area 6, Area 7 spring-ditch, and Hunter
Marsh. It is also found in a spring just
outside the BLNWR boundary on
private property owned by the City of
Roswell (G. Warrick 2005). Noel’s
amphipod was first described by Cole
(1981) from a 1967 collection of
amphipods taken from North Spring,
east of Roswell. Based on morphological
similarities, specimens collected from
Lander Springbrook near Roswell were
also identified as Noel’s amphipod (Cole
1981). The amphipod was extirpated
from Lander Springbrook between 1951
and 1960, and the North Spring
population was lost between 1978 and
1988. The extirpations were attributed
to regional groundwater depletions and
habitat alterations (spring
channelization) respectively (Cole 1981,
1985).
Previous Federal Actions
On November 22, 1985, we received
a petition from Mr. Harold F. Olson,
Director of the NMDGF, to add 11
species of New Mexican mollusks to the
Federal list of endangered and
threatened wildlife. Roswell springsnail
(Pyrgulopsis roswellensis, formerly
Fontelicella roswellensis (Hershler
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1994)), Koster’s springsnail (Juturnia
kosteri, formerly Durangonella kosteri
and Tryonia kosteri (Hershler et al.
2002)), and Pecos assiminea were
among the 11 species. We determined
that the petition presented substantial
information that the requested action
may be warranted and published a
positive 90-day petition finding in the
Federal Register on August 20, 1986 (51
FR 29671). A subsequent 12-month
finding published in the Federal
Register on July 1, 1987 (52 FR 24485),
concluded that the petitioned action
was warranted but precluded by other
higher priority listing actions.
On August 29, 2001, the Service
announced a settlement agreement in
response to litigation by the Center for
Biological Diversity, the Southern
Appalachian Biodiversity Project, and
the California Native Plant Society.
Terms of the agreement required that we
submit to the Federal Register, on or by
February 6, 2002, a 12-month finding
and accompanying proposed listing rule
and proposed critical habitat
designation for the four invertebrates
addressed in this final rule. This
agreement was entered by the court on
October 2, 2001 (Center for Biological
Diversity, et al. v. Norton, Civ. No. 01–
2063 (JR) (D.D.C.)). A proposed rule to
list the four invertebrates as endangered
with critical habitat was published in
the Federal Register on February 12,
2002 (67 FR 6459). On May 31, 2002, we
reopened the public comment period for
90 days (67 FR 6459). In addition, we
published newspaper notices inviting
public comment and announcing the
public hearing in the following
newspapers in New Mexico: the
Carlsbad Current-Argus, the Artesia
Daily Press, the Roswell Daily Record,
and the Albuquerque Journal. On June
18, 2002, we held a public hearing in
Carlsbad, New Mexico, to solicit
comments on the proposed rule.
On May 4, 2005, we announced the
availability of the draft economic
analysis and draft environmental
assessment for the proposal to designate
critical habitat for the four invertebrates
(70 FR 23083). Section 4(b)(2) of the Act
requires that we consider economic
impacts, impacts to national security,
and other relevant impacts prior to
making a final decision on what areas to
designate as critical habitat. We
solicited data and comments from the
public on these draft documents, as well
as on all aspects of our proposal, so that
we could consider these in this final
determination.
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Summary of Comments and
Recommendations
In the notices announcing the public
comment periods, we requested that all
interested parties submit comments on
the proposed listings and critical habitat
designation, as well as on the associated
draft economic analysis and draft
environmental assessment, and we also
requested information pertaining to any
actions that affect the four invertebrates;
their current status, ecology,
distribution, and threats; and
management or conservation efforts in
place. We requested this information in
order to make a final listing
determination based on the best
scientific and commercial data currently
available. We also solicited four
independent experts who are familiar
with these species to peer review the
proposed listing and critical habitat
designation. Two of the peer reviewers
submitted substantial comments, but
did not support or oppose the proposal.
During the public comment periods, we
also received 967 written comments
(952 written comments were identical,
in the form of automatically generated
emails), and 7 speakers gave verbal
comments at the public hearing. Of
those oral comments, one supported the
proposal, two were opposed to the
proposal, and four provided additional
information. Of the written comments,
956 supported the proposal, 8 were
opposed, and 3 were neutral but
provided information. All substantive
information provided during the public
comment periods, written and verbal,
either has been incorporated directly
into this final determination or is
addressed below. Similar comments are
grouped together by issue.
Issue 1: Biological Concerns
(1) Comment: It is unlikely that
Melanoides tuberculata, a fully aquatic
animal, competes with Pecos assiminea,
a semi-terrestrial species. On the other
hand, the presence of introduced
Melanoides tuberculata could pose a
serious threat to aquatic species such as
Koster’s springsnail, Roswell
springsnail, or Noel’s amphipod.
Our Response: The commenter is
correct. It is unlikely that Melanoides
would be a competitor with Pecos
assiminea and it is very likely that it
may be a serious threat to Koster’s
springsnail, Roswell springsnail, and
Noel’s amphipod. We have a more
complete discussion of the threat of
introduced species under the section,
‘‘Summary of Factors Affecting the
Species’’ below.
(2) Comment: The NMDGF concluded
in 1999 that all four invertebrate species
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are stable on the BLNWR. There is no
evidence that these species are at risk.
Our Response: All four invertebrates
are classified as Endangered by the
NMDGF under the Wildlife
Conservation Act of 1974 (i.e., State
Endangered Species Act) (19 NMAC
33.6.8). As such, the NMDGF supports
the listing and critical habitat
designation for these species. They
report that recent (1992 to present)
population and habitat monitoring on
BLNWR has documented the
persistence of these species; however,
they still face significant threats (Lang
2002, NMDGF 2005a). Our current
understanding of the threats to the four
invertebrates and their habitat are fully
described under the ‘‘Summary of
Factors Affecting the Species’’ section
below.
(3) Comment: Oil and gas
development activities in the vicinity of
BLNWR pose no threat to the four
invertebrates because the New Mexico
Oil Conservation Division regulations
for installation of oil and gas wells
provide protections to limit impacts.
Our Response: The New Mexico
Interstate Stream Commission (NMISC)
and NMDGF submitted information that
is consistent with the proposed rule,
which indicated oil and gas, residential,
or industrial development on the private
lands immediately west of BLNWR may
constitute a threat to spring water
quality (Balleau et al. 1999; McCord et
al. 2005; NMDGF 2005a) (see ‘‘Summary
of Factors Affecting the Species’’ section
below). The NMDGF also presented an
overview of oil and gas production and
potential risk to the four invertebrates
(NMDGF 2005a). They note that,
although there are no known cases of
groundwater contamination by leaking
oil or gas wells in the source-water
capture zone for the Middle Area of
BLNWR (discussed further under
‘‘Water Quality’’ section below),
groundwater contamination from
petroleum products has been
documented north of Roswell (NMDGF
2005a).
There is a history of oil and gas
industry operations on and adjacent to
BLNWR, which have resulted in the
spillage of oil and brine onto the
BLNWR. For example, annual reports
from 1994 to 1998 document four oil
and gas related accidents on and
immediately adjacent to BLNWR
(NMDGF 2002; NMISC 2002). In May
1993, a private corporation began
drilling a well on adjacent Bureau of
Land Management (BLM) lands when
they hit a water flow with a high
chloride content (6,000 parts per
million). The salt water was eventually
contained, but serves as an example of
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potential issues from oil and gas
development (Service 2002).
Additionally, in 1996, about 70 to 80
barrels of oil spilled within a berm on
an adjacent oil well located on BLM
lands (Service 2002). In 1997, an
additional 11 barrels of crude oil leaked
into the BLNWR boundary (Service
2002). In 1998, BLNWR personnel
documented probable violations of New
Mexico Oil Conservation Division
regulations (e.g., a substandard pit for
drilling cuttings, fire hazards, lack of
spillage notification) (Service 2002;
NMISC 2002). In 2000, there was an
additional oil spill on adjacent BLM
lands (NMISC 2002).
Development of another 91 natural
gas and oil wells has been anticipated
on lands managed by the BLM within
the source-water capture zone (NMDGF
2005a). Contamination of groundwater
from underground leaks has the
potential to occur in the future, but
existing drilling and casing regulations
by the State of New Mexico’s Oil
Conservation Division and requirements
of the BLM for oil and gas drilling and
operation in cave and karst areas (BLM
1997) are likely to substantially reduce
this probability. The NMDGF indicates
that a more likely pathway for
petroleum-product contamination of
groundwater is from leaking storage and
transport facilities from the well site
downstream to processing facilities
(NMDGF 2005a). These may include
leaking pipelines, overflowing storage
tanks, leaking valves, and other sources.
These data indicate that oil and gas
production and distribution continue to
threaten the four invertebrates.
(4) Comment: Contamination threats
to the four invertebrates are not limited
to oil and gas development, but also
include fire effects. Immediate and
short-term adverse effects have been
demonstrated from the March 2000
Sandhill Fire (NMISC 2002).
Our Response: NMDGF recently
reviewed the effects of fire on the
invertebrates (NMDGF 2005a). We agree
with their assessment and summarize
much of the information below. We
recognize that populations of these four
invertebrates have the potential to be
eliminated or habitat may be rendered
unsuitable if fire results in complete
combustion of vegetation and litter, high
soil temperatures, significant amounts
of ash flow, large changes in water
chemistry (e.g., dissolved oxygen), or
extensive vegetation removal resulting
in soil and litter drying. As such, we
have also revised the ‘‘Summary of
Factors Affecting the Species’’ section
below to include a more detailed
analysis on the threat of wildfire.
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(5) Comment: Much of the literature is
overly general in nature and is not siteor species-specific. Including such
citations leaves readers to conclude that
a particular author made a statement or
presented data that specifically applies
to the threats you believe exist for these
invertebrates.
Our Response: In determining and
evaluating threats to the four
invertebrates, we used the best scientific
and commercial data available. This
included articles published in peerreviewed journals, data collected by
NMDGF, and comments received on the
proposed rule, draft economic analysis,
and environmental assessment. You are
correct that some of our citations are not
specific to these species or the
geographic area. Nevertheless, the
citations offer evidence that certain
threats are real for the species because
similar examples have been
documented elsewhere.
(6) Comment: The allegation that fire
caused significant decreases in
invertebrate populations implies that
quantitative sampling was conducted.
The Service and NMDGF rarely conduct
quantitative sampling, and the case may
be overstated in your proposal.
Our Response: Extensive quantitative
pre- and post-fire monitoring was
conducted by the NMDGF (NMDGF
2005c). Immediately following the
Sandhill fire, Lang (2001) documented a
decrease in species richness of localized
populations of aquatic
macroinvertebrates. For example, in
1996 densities of Noel’s amphipod at
Dragonfly Spring were estimated at
11,625 per square meter (m2). Out of 74
post-fire monitoring collections
conducted from March 2000 to August
2004, only four Noel’s amphipod were
found (NMDGF 2005c).
(7) Comment: Does non-native
vegetation such as saltcedar (Tamarix
sp.) threaten the invertebrates? Will
New Mexico’s ability to eradicate or
manage saltcedar be restricted if these
species are listed?
Our Response: Saltcedar management
or eradication activities would be
subject to section 7 consultation
requirements if a proposed project has
the potential to affect the four
invertebrate species or designated
critical habitat. However, the
environmental assessment found that
some activities may be considered to be
of benefit to the four invertebrate
species (Service 2005). Examples of
such beneficial actions could include
removal and control of non-native
vegetation, restoration of wetlands, and
removal of non-native species.
Non-native saltcedar is present on
BLNWR and The Nature Conservancy
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46307
(TNC) lands at the Diamond Y Spring
and East Sandia Springs preserves
(Service 2005). This non-native species
is currently being controlled where
possible by BLNWR and TNC staff.
Control and removal of non-native
vegetation was identified as a factor
responsible for extirpation of localized
populations of Pecos assiminea in
Mexico and New Mexico (Taylor 1987).
However, it is possible that removal and
control of saltcedar will improve habitat
and hydrologic conditions at springs
and seeps (Service 2005). See also
‘‘Factor C’’ under the ‘‘Summary of
Factors Affecting the Species’’ section
below.
(8) Comment: Have laboratory toxicity
tests been conducted to determine the
four invertebrates’ sensitivity to low
oxygen, sediments, or contaminants?
Our Response: To our knowledge,
laboratory tests have not been
conducted specifically on these species
to determine their sensitivity to low
oxygen, sediments, or contaminants.
(9) Comment: Equating the
springsnails with Higgin’s eye mussel is
inappropriate. Clearly, clams and
mussels are very different creatures than
springsnails.
Our Response: The commenter is
correct that mussels that live in the
substrate and filter water to obtain
nutrition are very different from
springsnails that crawl on the substrate
and scrape periphyton (various forms of
algae and diatoms) off the substrate.
Unfortunately, very little research has
been done specifically on the effects of
contaminants on springsnails and
mussels are one of the most closely
related groups available for comparison.
However, this reference has been
removed from this final rule.
(10) Comment: The relevance of South
Spring River is not apparent in your
discussion of Noel’s amphipod. The
South Spring River has been dry for
many years.
Our Response: The discussion of
Noel’s amphipod and the dry South
Spring River was included to document
that this previously known population
has likely been extirpated.
(11) Comment: Are crayfish known
predators of springsnails?
Our Response: Crayfish are known to
consume aquatic macrophytes and algae
that springsnails rely on for grazing and
egg laying (Service 2004b). In addition,
crayfish have been cited as a threat and
are known to directly prey upon aquatic
invertebrates such as springsnails (e.g.,
Three Forks springsnail (Pyrgulopsis
trivialis)) (Arizona Game and Fish
Department 2003; Service 2004b).
Nevertheless, we have not observed any
crayfish within habitat occupied by
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these four invertebrates, with the
exception of Diamond Y Springs
Complex where an undescribed native
crayfish occurs. See also ‘‘Factor C’’
under the ‘‘Summary of Factors
Affecting the Species’’ section below.
(12) Comment: Effects to these species
from prolonged drought, nutrient
enrichment, and sedimentation are all
unsubstantiated.
Our Response: There is no doubt that
prolonged drought leading to spring
diminishment or drying would have a
negative impact on the invertebrates.
Little research has been done
specifically on springsnails to document
their response to elevated nutrients,
contaminants, or sedimentation.
However, based on biological principles
and effects observed in other related
invertebrates, we can draw reasonable
conclusions about what we would
expect to happen to these species.
(13) Comment: Have surveys for these
species been conducted at Bottomless
Lakes State Park?
Our Response: Surveys were
conducted on Bottomless Lakes State
Park during the 1990s by the NMDGF
and during the 1980s by D.W. Taylor.
Perennial sinks west-northwest of Lea
Lake and its outflow to the south, which
eventually flows to the BLM Overflow
Wetlands, were also surveyed for these
invertebrates (Lang 2005). Although
potentially suitable habitat for the four
invertebrates is available at Bottomless
Lakes State Park, these surveys failed to
document their occurrence (New
Mexico Energy Minerals and Natural
Resources Department 2000; NMDGF
2005b).
(14) Comment: A new population of
Noel’s amphipod has been recently
discovered on BLNWR.
Our Response: The commenter is
correct. Noel’s amphipod currently
persists on BLNWR at the Sago Spring
wetland complex (including Sinkhole
No. 31), Bitter Creek, and along the
western boundary of Area 6, in the west
ditch along Area 7, and along the
northwest fenceline of Hunter Marsh
(NMDGF 2005c). A new population was
discovered in 2004 in a spring belonging
to the City of Roswell that borders
BLNWR. This population is included in
the listing portion of this final rule, but
is not within the designation of critical
habitat. The critical habitat designation
does not include these private lands
because section 4(b)(4) of the Act and
the Administrative Procedure Act (5
U.S.C. 551 et seq.) requires that areas
designated as critical habitat must first
be proposed as such. Thus, we cannot
make additions in this final rule to
include areas that were not included in
the proposed rule. Designation of such
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areas would require a new or revised
proposal and subsequent final rule.
Should critical habitat be considered in
the future for the Noel’s amphipod, we
will consider this area in any such
determination.
(15) Comment: The ongoing drought
appears to be more of a threat to these
species than groundwater pumping.
Our Response: We agree. Please refer
to the ‘‘Summary of Factors Affecting
the Species’’ for further discussion of
this issue.
(16) Comment: The proposed rule
lacks documentation of groundwater or
surface contamination threats to the four
invertebrates.
Our Response: Based upon public
comments and information received, we
have updated our analysis to include
our current understanding of the threats
from groundwater or surface
contamination to the four invertebrates.
Please see the ‘‘Summary of Factors
Affecting the Species’’ section.
(17) Comment: The Pleistocene Era
was mentioned several times in the
proposed rule. Does the Service intend
to recover these species to levels that
were present during this historic era?
Our Response: No, section 4 of the
Act and its implementing regulations
(50 CFR part 424) set forth the
procedures for adding species to the List
of Endangered and Threatened Wildlife
and Plants. A species may be
determined to be endangered or
threatened due to one or more of the
five factors described in section 4(a)(1)
of the Act. As detailed below in our
analysis, we examine the listing factors
and their application to the four
invertebrates. The discussion of these
species in relation to the Pleistocene Era
was presented as evidence of an
apparent historical decline in the
numbers, range, and distribution. We
did not intend to suggest that the four
invertebrates need to be restored to
Pleistocene Era levels to be considered
recovered.
(18) Comment: Is there a plan to
control introduced or exotic snails or
other species that may prey upon or
compete with the four invertebrates?
Our Response: BLNWR is managed for
wildlife conservation, which includes
restoration and maintenance of
biological integrity, diversity, and
environmental health. Major land
management activities on BLNWR
include water level management in
impoundments to provide habitat for
waterfowl, shorebirds, and other groups
of species, habitat restoration,
prescribed burning, control of saltcedar,
and management of noxious weeds
(Service 2005a). Management or
removal of exotic species that compete
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with these invertebrates will be
evaluated in the development of a
recovery plan, but this management is
currently conducted as appropriate. For
example, removal of non-native fishes
from Diamond Y Springs Complex using
antimycin, netting, and trapping was
conducted in the past for conservation
of Leon Springs pupfish (Service 2005a).
For further information and analysis
concerning exotic species, please refer
to the ‘‘Factor C’’ under the ‘‘Summary
of Factors Affecting the Species’’
section.
Issue 2: Procedural and Legal
Compliance
(19) Comment: In the proposed rule
for the four invertebrate species,
restrictions are proposed on
groundwater pumping within the Pecos
Basin, which would have serious effects
on the water supply and use of water by
the citizens of New Mexico.
Our Response: We disagree, the
proposed rule did not propose
restrictions on groundwater pumping.
Consistent with our Interagency
Cooperative Policy for Endangered
Species Act Section 9 Prohibitions,
published in the Federal Register on
July 1, 1994 (59 FR 34272), we
identified in the proposed rule those
activities that we believe would or
would not constitute a violation of the
prohibitions identified in section 9 of
the Act. The final Federal listing of
these four invertebrates under the Act
requires that Federal agencies consult
with the Service on activities involving
Federal funding, a Federal permit,
Federal authorization,or other Federal
actions. Consultation (under section 7 of
the Act) is required when activities have
the potential to affect the four
invertebrates or designated critical
habitat. The consultation will analyze
and determine to what degree the
species are impacted by the proposed
action. Section 7 of the Act prohibits
actions funded, authorized, or carried
out by Federal agencies from
jeopardizing the continued existence of
a listed species or destroying or
adversely modifying the listed species’
critical habitat. This final Federal listing
does not restrict groundwater pumping
or any other actions.
The environmental assessment found
that spring flows within the proposed
critical habitat on BLNWR are already
protected by existing water rights
afforded by the New Mexico Office of
the State Engineer’s administration of
the Roswell Basin. In 1967, water rights
were adjudicated in the Roswell Basin,
wells were metered, and pumping rates
administered by the Office of the State
Engineer (OSE). Currently, any
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proposed change in use of water
(underground or surface depletion) in
the Roswell Basin will undergo analysis
by OSE to determine if there would be
impairment to existing water rights
(McCord et al. 2005). The OSE will not
allow such change if it impairs the
Federal water right in any respect
(NMISC 2005). Thus the spring flows on
BLNWR should be protected from any
changes in groundwater pumping near
the refuge in the future.
In Texas, Pecos assiminea currently
has no State or other regulatory
protection. Some protection for the
habitat of this species is provided with
the ownership of the springs by TNC
(Karges 2003). Groundwater pumping
that could affect spring flows is subject
to limited regulation in Texas. State
agencies do not control groundwater
pumping, and Texas courts have held
that, with few exceptions, landowners
have the right to take all the water that
can be captured under their land (rule
of capture), regardless of impacts to
neighbors or natural resources. As noted
in the economic analysis, within Texas
further hydrological studies are
necessary to determine the impact of
groundwater pumping on surface and
groundwater levels at Units 3 and 4. The
TNC has stated that additional research
on the delineation of watersheds is
crucial to the sustainable, long-term
conservation of the springs. If
hydrological studies determine a link
between the various aquifers, we would
work with private landowners on a
volunteer basis to minimize impacts to
the Pecos assiminea from groundwater
withdrawals.
(20) Comment: The groundwater
depletion analysis fails to rely upon the
best available science, does not utilize
an accurate and reliable model, and
mischaracterizes effects of groundwater
pumping.
Our Response: Based upon new
information we received during the
comment periods, we revised our
analysis from the proposed rule to
reflect our current understanding
regarding the threat of groundwater
depletion on the four invertebrates and
their habitat in New Mexico. Please
refer to the ‘‘Summary of Factors
Affecting Species’’ section.
(21) Comment: The status of these
species will not improve if they are
listed.
Our Response: Federal listing in and
of itself does not improve the status of
the species. Listing these species
authorizes the development of a
recovery plan. The recovery plan will
likely identify both State and Federal
efforts for conservation of these species
and establish a framework for agencies
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and stakeholders to coordinate activities
and cooperate with each other in
conservation efforts. The plan will set
recovery priorities and describe sitespecific management actions necessary
to achieve conservation and survival of
the four invertebrates. See also response
to comment 22 below for related
information about the five factors
described in section 4(a)(1) of the Act.
Also note the discussion on section 7
consultation requirements in our
response to comment 19 above.
(22) Comment: Why does the Service
want to list these four invertebrates
when they are already within protected
areas?
Our Response: We have analyzed the
threats to these species based upon the
five factors described in section 4(a)(1)
of the Act. Although these species occur
on areas that are currently managed for
conservation purposes, we have
determined based on our analysis of the
threats discussed below in the section
‘‘Summary of Factors Affecting the
Species,’’ that these four invertebrate
species are in danger of extinction
throughout all or a significant portion of
their respective ranges. Our analysis
determined that these species are
threatened by activities such as oil and
gas production and development,
groundwater pumping, and introduction
of non-native species that are beyond
the boundaries and/or the management
protected areas where the species are
found. Thus, the four invertebrates meet
the definition of endangered species.
(23) Comment: If these species are
listed, is there a possible effect to the
U.S. Bureau of Reclamation with respect
to delivery of irrigation water?
Our Response: Federal listing will
require the Bureau of Reclamation
(Reclamation) to consult with us on
activities that have the potential to
adversely affect the four invertebrates or
designated critical habitat. None of
Reclamation’s current projects will be
affected by the listing of the
invertebrates and we are not aware of
any future projects that may be affected
by the listing. Delivery of irrigation
water occurs via the Pecos River and we
do not anticipate that listing these
species will affect that activity.
(24) Comment: Will the listing of
these species impede the ability of the
State of New Mexico to meet Pecos
Compact River obligations?
Our Response: No, the NMISC has
been actively acquiring and leasing
water rights to meet the State’s delivery
obligations to Texas as specified in the
Pecos River Compact and pursuant to an
Amended Decree entered by the U.S.
Supreme Court. For example, between
1991 and 1999, $27.8 million was spent
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on the Pecos River water rights
acquisition program. We do not
anticipate that the listing of these
species or the designation of critical
habitat will alter the ability of the
NMISC to meet Pecos River Compact
delivery obligations. The amount of
water being pumped from the Roswell
Basin should not change; however, the
use of water will change. For example,
instead of being applied to fields, the
water may be delivered to the Pecos
River directly to meet Compact delivery
obligations.
(25) Comment: Will oil and gas
exploration be further restricted in areas
designated as critical habitat?
Our Response: No, the Service does
not anticipate that the designation of
critical habitat will restrict oil and gas
exploration. Section 7 consultation,
when required, would analyze any
impacts to the species and their
designated critical habitat. The
environmental assessment found that oil
and gas projects with Federal
involvement in the BLNWR and the
surrounding area are already subject to
stipulations for protecting groundwater
(Service 2005). The Oil Conservation
Division of the New Mexico Energy,
Minerals, and Natural Resources
Department regulates oil and gas well
drilling and casing in part to prevent
contamination of groundwater (19
NMAC 15.3).
BLNWR is excluded from the
designation of critical habitat for the
four invertebrate species, and critical
habitat would not result in additional
section 7 consultations on federally
supported oil and gas projects. Oil and
gas well development in the vicinity of
Diamond Y Springs Complex and East
Sandia Spring occurs on private lands
with no Federal involvement. Therefore,
section 7 consultations on the effects to
designated critical habitat would likely
not occur for these projects. For this
reason, we do not believe there would
be any additional restrictions to oil and
gas exploration activities.
Issue 3: National Environmental Policy
Act (NEPA) Compliance and Economic
Analysis
(26) Comment: What has regulation or
policy of Federal actions cost State and
County governments before listing and
critical habitat designation?
Our Response: Since the proposed
listing of the four invertebrates species,
there have been specific conservation
actions implemented that have taken
into account the protection of the
species. An estimated $366,000 to
$494,000 in costs have been incurred by
Federal and State agencies for the four
invertebrates (Service 2005b). These
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costs are related to developing the New
Mexico State recovery plan and have
included monitoring the four
invertebrates’ habitat, consultant fees,
staff time devoted to developing the
plan, administrative costs related to past
conferences under section 7 of the Act,
and associated monitoring of
invertebrate habitat. We did not find
that County governments have incurred
any costs related to the conservation of
these species.
(27) Comment: Does the Service have
an estimate of the costs required to
recover the four invertebrates?
Our Response: The costs of actions to
recover the four invertebrates will be
estimated during the development of a
recovery plan.
(28) Comment: The economic analysis
should consider benefits of the critical
habitat designation.
Our Response: In the context of a
critical habitat designation, the primary
purpose of the rulemaking (i.e., the
direct benefit) is to designate areas that
have the features on which the species
depend and that are in need of special
management.
The designation of critical habitat
may result in two distinct categories of
benefits to society: (1) Use benefits; and
(2) non-use benefits. Use benefits are
simply the social benefits that accrue
from the physical use of a resource.
Visiting critical habitat to see
endangered species in their natural
habitat would be a primary example.
Non-use benefits, in contrast, represent
welfare gains from ‘‘just knowing’’ that
a particular listed species’’ natural
habitat is being specially managed for
the survival and recovery of that
species. Both use and non-use benefits
may occur unaccompanied by any
market transactions.
A primary reason for conducting an
economic analysis is to provide
information regarding the economic
impacts associated with a proposed
critical habitat designation. Section
4(b)(2) of the Act requires the Secretary
to designate critical habitat based on the
best scientific data available after taking
into consideration the economic impact,
impact to national security, and any
other relevant impact, of specifying any
particular area as critical habitat.
Economic impacts can be both positive
and negative and by definition, are
observable through market transactions.
Where data are available, the
economic analysis attempts to recognize
and measure the net economic impact of
the proposed designation. For example,
if the fencing of a species’ habitat to
restrict motor vehicles results in an
increase in the number of individuals
visiting the site for wildlife viewing,
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then the analysis would recognize the
potential for a positive economic impact
and attempt to quantify the effect (e.g.,
impacts that would be associated with
an increase in tourism spending by
wildlife viewers). In this particular
instance, however, the economic
analysis did not identify estimates or
measures of positive economic impacts
that could offset some of the negative
economic impacts analyzed earlier in
this analysis.
While the Act requires the Service to
specifically consider the economic
impact of a designation, it does not
require the Service to explicitly
consider any broader social benefits (or
costs) that may be associated with the
designation. In fact, the Service believes
that this is by Congressional design,
because the Act explicitly states that it
is the Federal government’s policy to
conserve all threatened and endangered
species and the ecosystems upon which
they depend. While section 4(b)(2) of
the Act gives the Secretary discretion to
exclude certain areas from the final
designation, she is authorized to do so
only if an exclusion does not result in
the extinction of the species. Thus, the
Service believes that explicit
consideration of broader social values
for the species and its habitat, beyond
economic impacts, is not necessary as
Congress has already clarified the
importance our society places on
conserving all threatened and
endangered species and their natural
habitats upon which they depend. In
terms of carrying out its responsibilities
under section 4(b)(2) then, the Service
need only consider whether the
economic impacts (both positive and
negative) are significant enough to merit
exclusion of any particular area without
causing the species to go extinct.
(29) Comment: The economic analysis
overstates costs by including past costs
that occurred before the species was
listed, costs that would result from the
listing alone, and costs that derive from
conservation efforts for other listed
species. Similarly, the economic
analysis includes costs of consultation
with the Environmental Protection
Agency (EPA) regarding Concentrated
Animal Feeding Operations (CAFOs),
which should be primarily associated
with other listed species, and the listing
of the four invertebrates, and not critical
habitat designation.
Our Response: This analysis identifies
those economic activities believed to
most likely threaten the four
invertebrates and their habitat and,
where possible, quantifies the economic
impact to avoid, mitigate, or compensate
for such threats within the boundaries
of the critical habitat determination. The
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economic analysis considers past
impacts associated with species
conservation efforts that have been
incurred since the proposed listing and
critical habitat determination in 2002.
The impact of these efforts is considered
relevant to understanding the potential
impact of the listing and critical habitat
determination. Further, due to the
difficulty in making a distinction
between listing and critical habitat
effects within critical habitat
boundaries, this analysis considers all
future conservation-related impacts to
be coextensive with the designation.
The consideration of co-extensive
costs was mandated by the 10th Circuit
Court of Appeals ruling in the New
Mexico Cattle Growers Association case
(248 F.3d at 1285), which directed us to
consider all impacts, ‘‘regardless of
whether those impacts are attributable
co-extensively to other causes.’’ As
explained in the economic analysis, due
to possible overlapping regulatory
schemes and other reasons, there are
also some elements of the analysis
which may overstate some costs.
Conversely, the 9th Circuit has
recently ruled (‘‘Gifford Pinchot,’’ 378
F.3d at 1071) that the Service’s
regulations defining ‘‘adverse
modification’’ of critical habitat are
invalid because they define adverse
modification as affecting both survival
and recovery of a species. The Court
directed us to consider that adverse
modification should be focused on
impacts to recovery. While we have not
yet proposed a new definition for public
review and comment, changing the
adverse modification definition to
respond to the Court’s direction may
result in additional costs associated
with critical habitat definitions
(depending upon the outcome of the
rulemaking).
As described in section 1.2 of the
economic analysis, coextensive effects
may also include impacts associated
with overlapping protective measures of
other Federal, State, and local laws that
aid habitat conservation in the areas
proposed for designation, including
protections for other listed species.
These measures may be in part
precipitated by the consideration of the
presence of the species and impending
critical habitat determination. Because
the quantified habitat conservation
efforts, regardless of their primary
impetus, afford protection to the four
invertebrates, they likely contribute to
the efficacy of the critical habitat
determination efforts. The impacts of
these actions are therefore considered
relevant for understanding the full effect
of the proposed critical habitat
determination. Enforcement actions
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taken in response to violations of the
Act, however, are not included.
(30) Comment: The economic analysis
inappropriately includes costs of delays
in proposed drilling operations
associated with industry appeals on
applications for drilling permits. The oil
and gas industry, however, is appealing
environmental protections associated
with their permits and burdening
themselves. This should not be included
as a cost of the critical habitat
designation.
Our Response: Industry appeals
regarding drilling applications are a
result of the implementation of
environmental regulations, including
the Act, that recommend additional
species and habitat conservation efforts
be undertaken with the drilling activity.
The economic impacts of these delays
are therefore considered relevant in
understanding the impact of
conservation efforts for the four
invertebrates.
(31) Comment: It is unclear from the
economic analysis what additional
protections from oil and gas activities
may be provided by the Service for the
four invertebrates as the economic
analysis includes costs associated with
the listing and with protections for other
species, but no additional costs
associated specifically with the critical
habitat designation.
Our Response: This analysis identifies
the types of modifications to economic
activities that may be undertaken to
avoid, mitigate, or compensate for
threats to the species and habitat. The
draft economic analysis acknowledges
the difficulty in distinguishing between
listing and critical habitat effects and
therefore considers all future
conservation-related impacts to be
coextensive with the critical habitat
designation. Further, the relative level
to which multiple considerations,
including that of other species,
contribute to the undertaking of a
conservation effort is unclear. The
impacts quantified in the analysis are
assumed to be in some part precipitated
by the critical habitat designation for the
four invertebrates. Absent information
on the specific increment by which
critical habitat designation contributes
to the undertaking of these efforts, the
total impact of the effort is quantified,
and not a fraction solely due to critical
habitat designation.
(32) Comment: The draft economic
analysis relies on information provided
by impacted industries to quantify the
costs to those industries. These costs are
inflated. For example, environmentally
protective project modifications such as
closed-loop systems can result in cost
savings to the oil and gas industry. The
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draft economic analysis, however, only
includes the costs to the industry of
modifying projects to incorporate
conservation measures for the species.
Our Response: As the commenter
notes, the potential for cost savings
associated with implementing
environmentally protective
technologies, such as closed-loop
systems, is acknowledged in the draft
economic analysis on page 4–7.
However, the level of benefit these
modifications may generate is unclear.
Additionally, application of closed-loop
systems is not ubiquitous. As the
industry indicates, it is not always the
most beneficial operations alternative.
The draft economic analysis therefore
includes the full cost of this
modification to oil and gas operations as
a high-end estimate of the impact of
conservation efforts.
(33) Comment: The NMDGF’s 2004
Biennial Review of threatened and
endangered species in the State
indicated that off-refuge land use
practices within areas of the Roswell
Artesian Basin (RAB), such as regional
groundwater pumping for agriculture,
municipal water supplies, and the oil
and gas industries, threaten the
invertebrate species. In contrast, a
recent report prepared by the New
Mexico Office of the State Engineer
(OSE) provides the most recent
information regarding the hydrology of
the RAB. The report concludes that
‘‘* * * an extended, extreme drought,
and not groundwater depletion through
human activity, would potentially
threaten the future supply of water for
the proposed critical habitat located
within the BLNWR.’’
Our Response: Paragraph 77 and
section 4.2.2 of the draft economic
analysis state that no hydrologic models
currently exist to determine the impact
of groundwater pumping of the RAB on
the springs at the BLNWR. The revised
economic analysis acknowledges recent
information resulting from the OSE
report. As the draft economic analysis
does not quantify impacts of critical
habitat designation to groundwater
pumping; however, the quantitative
results of this analysis are unchanged as
a result of this comment.
Summary of Changes From the
Proposed Rule
Based upon our review of the public
comments, the economic analysis,
environmental assessment, issues
addressed at the public hearing, and any
new relevant information that may have
become available since the publication
of the proposal, we reevaluated our
proposed listing and critical habitat
designation and made changes as
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appropriate. Other than minor
clarifications and incorporation of
additional information on the species’
biology, this final rule differs from the
proposal by:
(1) The exclusion of critical habitat on
BLNWR because special management
considerations are currently provided to
the four invertebrates through current
BLNWR management; and
(2) Changes to the primary constituent
elements of critical habitat for the Pecos
assiminea.
Summary of Factors Affecting the
Species
Section 4 of the Act and
implementing regulations (50 CFR 424)
set forth the procedures for adding
species to the Federal lists. A species
may be determined to be threatened or
endangered due to one or more of the
five factors described in section 4(a)(1)
of the Act. These factors and their
application to the Roswell springsnail,
Koster’s springsnail, Pecos assiminea,
and Noel’s amphipod are as follows.
A. The present or threatened
destruction, modification, or
curtailment of its habitat or range.
Several biological traits of a
population have been identified as
putting a species at risk of extinction
(McKinney 1997; O’Grady 2004). Some
of these characteristics include having a
localized range, limited mobility, and
fragmented habitat (McKinney 1997;
O’Grady 2004). The four invertebrates
have all of these characteristics. Having
a small, localized range means that any
perturbation, either natural (e.g.,
drought) or anthropogenic (e.g., water
contamination) can eliminate many or
all of the existing populations. Having a
high number of individuals at a site
provides no protection against
extinction. Noel (1954) noted that the
amphipod in Lander Spring was the
most abundant animal present. It was
extirpated from that site when the
spring dried up (Cole 1985). The range
reduction trend in these snail species
(e.g., by extirpation of once widely
distributed but localized populations) is
supported by the Pleistocene fossil
record in conjunction with re-inventory
of known site occurrences in which no
individuals were detected (Noel 1954;
Taylor 1987; Mehlhop 1992, 1993;
NMDGF 1999). Fossil records indicate
that at least one or more of these snail
species were historically found at
Berrendo Creek, North Spring, and
South Spring Rivers, and along the
Pecos River (NMDGF 1999). This
evidence suggests an apparent historical
decline in the numbers, range, and
distribution of these species.
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Limited mobility restricts the ability
of the invertebrates to find and disperse
to other suitable habitats or to move out
of habitat that becomes unsuitable.
Consequently, their range remains
restricted and they are unable to avoid
contaminants or other unfavorable
changes to their habitat. Fragmented
(unconnected) habitat restricts gene
flow among populations and limits the
ability of the invertebrates to recolonize
habitats that have been disturbed but
then recover. For example, three springs
once contributed to Berrendo Creek in
the Roswell Basin. If the population of
springsnails in one of the springs was
eliminated because of a toxic spill, after
the habitat had recovered, the spring
could have been colonized naturally by
dispersal of animals from the other
springs. In the currently fragmented
habitats, dispersal is highly unlikely
and if a population is extirpated the
habitat probably will not be recolonized,
further restricting the range.
In addition to the characteristics
listed above that may put species at
greater risk of extinction, habitat loss,
introduced species, and habitat
degradation can also lead to extinction
(Meffe et al. 1994; Frankham et al.
2002). Each of these topics is discussed
in detail. Curtailment of range and
habitat of the four invertebrates has
occurred primarily through the loss of
suitable spring habitat. These species
were most likely much more widely
distributed throughout the Pecos River
Basin during the wetter climatic period
of the Pleistocene. As the climate
became warmer and drier, the
invertebrates were restricted to the
remaining free-flowing springs. Fossil
records indicate that two of the snail
species were found at Berrendo Creek
and along the Pecos River (Taylor 1987).
In addition, in the late 1800s, flow at
North Spring, South Spring, and
Berrendo Creek was 85 cubic feet per
second (cfs) (2.4 cubic meters per
second [cms], 60 cfs (1.7 cms), and 66
(1.9 cms) cfs, respectively (Fiedler and
Nye 1933). These systems each provided
abundant habitat for the invertebrates.
Lander Spring, a tributary spring of
South Spring, harbored Noel’s
amphipod (Noel 1954). The historic
connection of these spring systems to
the Pecos River most likely facilitated
dispersal of the invertebrates throughout
the basin downstream of this area.
In the 1880s, irrigated agriculture in
the Roswell and Artesia Basins was
limited to a few small farms (Fielder
and Nye 1933). By the end of 1905, 485
artesian wells had been drilled and by
1927, 1,424 wells were pumping water
(Fiedler and Nye 1933). One well,
drilled for the Oasis Cotton Company, is
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estimated to have produced 9,000
gallons/minute (20 cfs) (Fiedler and Nye
1933, Jones and Balleau 1996). As a
result of extensive groundwater
pumping, the artesian head in the basin
declined (Fiedler and Nye 1933). The
amount of decline depended on location
within the basin and ranged from 32 to
204 feet (9.7 to 62.2 meters) from
original levels by 1927, and led to a
decrease in area within the basin that
had artesian flow (Fiedler and Nye
1933). Groundwater depletion
continued until the mid-1970s, when it
reached its maximum (McCord et al.
2005).
By 1926, South Spring was dry (Jones
and Balleau 1996). Berrendo Spring still
produced 8.3 cfs, about 12 percent of
the original 1880s flow (Jones and
Balleau 1996). Today, Berrendo Well
produces less than 1 cfs (McCord et al.
2005). Lander Spring went dry in the
late 1950s or early 1960s (Cole 1981),
extirpating the population of Noel’s
amphipod, which in the early 1950s had
been described by Noel (1954) as the
most abundant animal in the spring.
Discharge at North Spring is unknown.
Jones and Balleau (1996) list its flow as
0 in 1926, but Cole (1981) described 3
small separate brooks that entered a
pond on a private golf course in 1967.
Surveys in 1995 at the site indicated
that Roswell springsnail and Koster’s
springsnail were still present at the
location (Noel’s amphipod once
occupied the site). Surveys in 2004
found none of the species, most likely
due to habitat modification from pond
enlargement (NMDGF 2005a). Surface
flow at BLNWR was also diminished by
artesian pumping. Springs adjacent to
Salt Creek no longer flow, and surface
flow from the Middle Area of BLNWR
(sum of flow in upper Bitter Creek and
Middle Area springs) was 15 cfs (0.4
cms) in 1937 and 5 cfs (0.14 cms) in
1995 (Jones and Balleau 1996). Aerial
photos which show a larger, meandering
channel for Bitter Creek are also
evidence that discharge from Bitter
Creek was once greater.
Groundwater pumping in the Roswell
Basin led to the drying of several
springs, many of which are known to
have harbored one or more of the four
invertebrates. It is not possible to
determine the extent of the loss of
invertebrate populations because many
springs went dry long before these
species were described or surveys could
be conducted. Members of the family
Hydrobiidae (including Pyrgulopsis) are
susceptible to extirpation or extinction
because they often occur in isolated
desert springs (Hershler 1989; Hershler
and Pratt 1990; Hershler 1994; Lydeard
et al. 2004). At least three species in this
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genus have gone extinct (Hershler 1994).
In addition, loss can not be measured
simply by the number of artesian
springs that are now not flowing. Many
of these springs were large enough to
form rivers that flowed for several miles
and creeks such as Bitter Creek, while
still flowing, are reduced in length.
Most likely there was suitable habitat
available for the invertebrates
throughout the length of the streams.
Groundwater pumping in the Roswell
Basin increased through the 1950s,
when approximately 450,000 acre feet/
year were extracted (McCord et al.
2005). Rates remained fairly stable
through 1966 (McCord et al. 2005). In
1967, water rights were adjudicated in
the Roswell Basin, wells were metered,
and pumping rates administered by the
Office of the State Engineer (OSE).
Currently, any proposed change in use
of water (underground or surface
depletion) in the Roswell Basin will
undergo analysis by OSE to determine if
there would be impairment to existing
water rights (McCord et al. 2005). The
OSE will not allow such change if it
impairs the Federal water right in any
respect (NMISC 2005). Thus the spring
flows on BLNWR should be protected
from any changes in groundwater
pumping near the Refuge in the future.
There was a drought in the 1950s that
most likely affected the recharge of the
groundwater in the Roswell Basin. In
spite of controls on pumping initiated in
1968 and increased precipitation near
Roswell in the 1960s and 1970s, artesian
groundwater levels continued to decline
until 1975 (McCord et al. 2005). Thus,
it appears that there was a lag between
the time of the drought and recovery in
the artesian groundwater. Since 1999,
New Mexico has been in a drought
(Piechota et al. 2004). The current
drought may also affect groundwater
recharge but there may be a lag before
the effect of the current drought is seen.
However, through the drought of the
1950s, when pumping was at a
maximum, several of the springs on
BLNWR continued to flow (McCord et
al. 2005). Groundwater pumping is
currently about 100,000 acre feet/year
less than it was during the drought of
the 1950s and artesian groundwater
levels have recovered to the levels they
were at in 1950s (McCord et al. 2005).
Consequently, we expect that there is
some added margin of protection for the
springs through this current drought.
However, the length or severity of the
current drought cycle is not known and
the Southwest may be entering a period
of prolonged drought (MaCabe et al.
2004). Droughts of the twentieth century
were eclipsed in severity by droughts in
the last 2000 years, with some
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characterized by longer duration
(multidecadal) and greater spatial extent
(Woodhouse and Overpeck 1998;
Piechota et al. 2004). Certainly, without
groundwater pumping or with pumping
at reduced volume there would be a
greater margin of safety for the springs.
But the evidence suggests that the
springs at BLNWR will flow in spite of
relatively intense drought (i.e.,
comparable to the drought of the 1950s)
(McCord et al. 2005). It is unknown how
the springs in Texas would respond to
extended drought and the current level
of groundwater pumping.
Drought could affect the springs
through decreased flow. The springs do
not have to dry out completely to have
an adverse effect on populations.
Droughts impact both surface and
groundwater resources and can lead to
diminished water quality and disturbed
riparian habitats (Woodhouse and
Overpeck 1998; MacRae et al. 2001).
Decreased flow could lead to a decrease
in habitat availability, increased water
temperatures, lower dissolved oxygen
levels, and an increase in salinity
(MacRae et al. 2001). Any of these
factors, alone or in combination, could
lead either to the reduction or
extirpation of a population.
The primary threat to Pecos assiminea
in Texas is the potential failure of spring
flow due to excessive groundwater
pumping and/or drought, which would
result in total habitat loss for the
species. Diamond Y Spring is the last
major spring still flowing in Pecos
County, Texas (Service 2005c). Pumping
of the regional aquifer system for
agricultural production of crops has
resulted in the drying of most other
springs in this region (Brune 1981).
Other springs that have already failed
include Comanche Springs, which was
once a large spring in Fort Stockton,
Texas, about 12.9 km (8 mi) from
Diamond Y. Comanche Springs flowed
at more than 142 cfs (4.0 cms) (Brune
1981) and undoubtedly provided habitat
for rare species of fishes and
invertebrates, including springsnails.
The spring ceased flowing by 1962
(Brune 1981) except for brief periods
(Small and Ozuna 1993). Leon Springs,
located upstream of Diamond Y in the
Leon Creek watershed, was measured at
18 cfs (0.5 cms) in the 1930s and was
also known to contain rare fish, but
ceased flowing in the 1950s following
significant irrigation pumping (Brune
1981). There have been no continuous
records of spring flow discharge at
Diamond Y Spring by which to
determine any trends in spring flow.
Studies by Veni (1991) and Boghici
(1997) indicate that the spring flow at
Diamond Y Spring may come from the
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Rustler aquifers located west of the
spring outlets. One significant factor
that influences flows at the spring is the
large groundwater withdrawals for
agricultural irrigation of farms to the
southwest in the Belding-Fort Stockton
areas. Although TNC of Texas owns and
manages the property surrounding the
Diamond Y Springs Complex, it has no
control over groundwater use that
affects spring flow.
East and West Sandia Springs are at
the base of the Davis Mountains just east
of Balmorhea, Texas, and are part of the
San Solomon-Balmorhea Spring
Complex, the largest remaining desert
spring system in Texas where the Pecos
assiminea is found. The springs are
included in a 97-hectare (ha) (240-acre
(ac)) preserve owned and managed by
TNC (Karges 2003). East Sandia Spring
discharges at an elevation of 977 meters
(3,224 feet) from alluvial sand and
gravel (Schuster 1997). Brune (1981)
noted that flows from Sandia Springs
were declining. East Sandia may be very
susceptible to over pumping in the area
of the local aquifer that supports the
spring. Measured discharges in 1995
and 1996 ranged from 0.45 to 4.07 cfs
(0.013 to 0.11 cms) (Schuster 1997). The
small outflow channel from East Sandia
Spring has not been significantly
modified and water flows into an
irrigation system approximately 100 to
200 meters (328 to 656 feet) after
surfacing. West Sandia Spring also
occurs on the TNC preserve, but it
ceased flowing in the past 10 years
(Schuster 1997).
Phantom Lake Spring , another spring
near the Sandia Springs, has
experienced a longterm, consistent
decline in flow. Discharge data have
been recorded from the spring six to
eight times per year since the 1940s by
the U.S. Geological Survey (Schuster
1997). The record shows a steady
decline of flows, from greater than 10
cfs (0.28 cms) in the 1940s to 0 cfs in
2000. The exact causes for the decline
in flow from Phantom Lake Spring are
unknown. Some of the obvious reasons
are groundwater pumping of the
supporting aquifer and decreased
recharge of the aquifer from drought
(Sharp et al. 1999; Sharp et al. 2003).
The Texas Water Development Board
(2005) concluded that because of the
uncertainties of the regional flow
system, it is difficult to assess why
spring flow in Phantom Lake Spring has
declined. Ashworth et al. (1997) noted
the improper placement of new wells
could have a detrimental effect on the
springs. The Texas Water Development
Board (2005) agreed with this
conclusion. Because of the regional
scale of the base flow, slow travel time,
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46313
and the age of the waters issuing from
the spring system, it is anticipated that
any substantial pumping in the regional
flow system will cause a decline in the
spring flow in the San Solomon Springs
system (including Phantom Lake, San
Solomon, Giffin, and East Sandia
springs) (Texas Water Development
Board 2005).
Introduced Species
One threat not thoroughly explored in
our proposed listing is that of
introduced species. Introduced species
are one of the primary threats
contributing to species’ extinction
(Pimentel et al. 2000; Frankham et al.
2002) and are one of the most serious
threats to native aquatic species
(Williams et al. 1989; Lodge et al. 2000),
especially in the Southwest (Miller et al.
1989; Minckley and Douglas 1991). It is
estimated that approximately 50,000
non-native species have been
introduced into the United States
(Pimentel et al. 2000). While some of
these introductions have been
beneficial, many have caused dramatic
declines in populations of native plants
and animals (Pimentel et al. 2000).
Because the distribution of the four
invertebrates is so limited, and their
habitat so restricted, introduction of a
non-native species into their habitat
could be devastating. Several non-native
species have been very successful in
invading spring ecosystems in the
Southwest. For that reason, we discuss
several invasive terrestrial and aquatic
animal species that are present in the
invertebrates’ habitat or are not yet
present but have caused problems in
other similar habitats in the Southwest
and would pose a threat to the four
invertebrates if they were introduced.
Several invasive terrestrial plant
species that may affect the invertebrates
are present at BLNWR: saltcedar
(Tamarix ramossisima), common reed
(Phragmites australis), and Russian
thistle (tumbleweeds) (Salsola spp.). In
addition, one non-native, terrestrial
snail species (Rumina decollata) will be
discussed. These plants present unique
challenges and threats to the habitat the
four invertebrates occupy. Eradication
of saltcedar is an ongoing management
effort at BLNWR and on TNC property
at Diamond Y Spring and East Sandia
Springs preserves (Service 2005). The
species is removed mechanically by
hand (young sprouts), with heavy
equipment for large trees, by cutting and
burning, or by spraying with herbicides.
Control and removal of non-native
vegetation has previously been
identified as a factor responsible for
extirpation of localized populations of
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Pecos assiminea in Mexico and New
Mexico (Taylor 1987).
Saltcedar is seen as a threat to the
spring habitats primarily through the
amount of water it consumes and from
the chemical composition of the leaves
it drops on the ground and into the
springs. Invertebrates in small spring
ecosystems depend on food from two
sources: that which grows in or on the
substrate (aquatic plants, algae, and
periphyton) and that which falls or is
blown into the system (primarily
leaves). Leaves from non-native plants
that fall into the water are often less
suitable food sources for invertebrates
because of either their resins or their
physical structure (Bailey et al. 2001).
Saltcedar leaves add salt to the soil
through its leaf litter (the leaves contain
salt glands) (DiTomosoa 1998). Because
saltcedar grows along the edge of water
courses, it is possible that this could
affect the soil chemistry of areas
inhabited by Pecos assiminea. However,
no research has been conducted
specifically on the effect of saltcedar on
Pecos assiminea.
The concentration of common reed at
BLNWR has been increasing over the
last few years and was seen to increase
significantly in Bitter Creek after the
Sandhill fire in 2000 (NMDGF 2005b,
2005c). It is unknown if the common
reed present at BLNWR is of native
origin or if it is introduced. Common
reed grows in dense patches and
reproduces primarily through an
underwater rhizome (an elongated,
horizontal stem). Dense stands of the
plant choke the channel, slowing water
velocity and creating more pool-like
habitat. Pool-like habitat is less suitable
for the Roswell and Koster’s
springsnails, which prefer flowing
water. In addition, the dense stands of
the plant can completely shade the
water, inhibiting algal growth, one of
the food items for the springsnails.
Russian thistle (tumbleweed) is
another introduced plant species that
can create problems within the spring
ecosystem. Russian thistle is not a
riparian species like saltcedar and
common reed; however, it often ends up
in the springs because wind blows the
tumbleweeds into the spring channels.
Noel (1954) noted that she had to pull
Russian thistle out of Lander Spring so
that she could take samples. In 2005,
BLNWR conducted an emergency IntraService section 7 consultation for the
removal of tumbleweeds from the Area
6 spring ditch. Wind had blown the
tumbleweeds into the channel to a
depth of 0.9 to 1.2 meters (3–4 feet),
completely shading the water and overloading the small channel with organic
material. While some amount of organic
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material from outside the spring
ecosystem is necessary and desirable, it
is not desirable to overload the system
with so much organic material that it
cannot be processed. In such situations,
dissolved oxygen can drop to
dangerously low levels as the material
decomposes. Primary productivity
(growth of algae and native aquatic
plants like watercress) would be greatly
reduced or prevented because of
shading. Control of introduced
terrestrial plant species is an on-going
management activity at BLNWR that
will have to be conducted carefully to
have the least impact on the four
invertebrates and their habitat.
Water Quality
These four species depend upon
water for their survival. Therefore, water
contamination is one of the most serious
threats to these species. In order to
assess the potential for water quality
contamination, a study was completed
in September 1999 to determine the
sources of water for the springs at
BLNWR. This study (Balleau et al. 1999)
reported that the source of water that
will reach the BLNWR springs over time
periods ranging from 10 to 500 years
includes a broad area beginning west of
Roswell near Eightmile Draw, extending
to the northeast to Salt Creek, and
southeast to the BLNWR. Since this area
delineates the groundwater source area
of surface water on the BLNWR, it
likewise represents pathways for
contaminants to enter the species’
habitat. This broad area sits within a
portion of the Roswell Basin and
contains a mosaic of Federal, State, and
private lands with multiple land uses,
including expanding urban
development.
Contamination of groundwater
sources from industry and commercial
operations in and around Roswell is
well documented. For example,
perchloroethylene (PCE) was discovered
in the McGaffey and Main groundwater
plume in Roswell in 1994
(Environmental Protection Agency
(EPA) 2001a, 2001b). It is suspected that
a dry cleaning facility that operated
from 1956 to 1963 is the source of the
PCE. The New Mexico Environment
Department subsequently detected PCE
in 13 of 16 groundwater wells in a 1995
investigation (EPA 2001a, 2001b).
Trichloroethylene was detected in
alluvial and artesian aquifers on the
south side of Roswell, at the former site
of the Walker Air Force Base, beginning
in 1991 (U.S. Army Corps of Engineers,
https://www.spa.usace.army.mil/ec/
walker-rab/projectinfo.html). Although
there is no indication that either of these
contaminants will enter springs
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occupied by the four invertebrates, these
examples demonstrate that groundwater
contamination can easily occur and
have long-lasting effects.
Sediments and fish from Hunter
Marsh, located on BLNWR, which
received municipal wastewater from the
City of Roswell, have elevated
concentrations of polychlorinated
biphenyl (PCB), polycyclic aromatic
hydrocarbons (PAHs), selenium, copper,
lead, zinc, and mercury (MacRae et al.
2001; Lusk 2005). Fish collected from
Hunter Marsh and Hunter Oxbow
contained PCB concentrations as high as
5 parts per million (ppm) (MacRae et al.
2001; Lusk 2005). A diet that contains
more than 0.1 ppm total PCBs can have
adverse effects on wildlife (MacRae et
al. 2001). PAHs were found at
concentrations as high as 7 ppm in
sediment and fish, which exceeds
criteria known to cause adverse effects
to aquatic organisms (MacRae et al.
2001). Values of PCBs in sediment
collected from Hunter Marsh are at
levels associated with approximately 30
percent mortality to invertebrates
(amphipods) (MacDonald et al. 2000;
Ingersoll et al. 2000; Lusk 2005).
Urban development on the west side
of BLNWR poses a risk to ground and
surface water quality from sewage
contamination (i.e., septic discharge).
The largest source of groundwater
contamination in New Mexico is from
household septic tanks and leach fields
(NM Water Quality Control Commission
2002). Common pollutants associated
with septic tank contamination include
total dissolved solids, iron, manganese,
sulfides, nitrate, organic chemicals, and
microbiological contaminants such as
bacteria viruses and parasites (NM
Water Quality Control Commission
2002). Septic leachate is known to have
contaminated groundwater resources in
New Mexico (McQuillan et al. 1989);
however, specific events have not been
documented near BLNWR. Sinkholes
west of BLNWR have been used for
unregulated domestic refuse dumping.
Refuse in the sinkholes has included
domestic contaminants such as
pesticides, herbicides, and waste oil
(Lang 2002). The extent of groundwater
contaminants generated from residences
and illegal dumps near the BLNWR is
unknown.
Wastewater from concentrated animal
areas (e.g., dairies, feed lots, chicken
farms), septic tanks, and agricultural
uses is a known contributor of nitrates
to surface and underground water
sources (Boyer and Pasquarell 1995).
Nitrate levels in the underground
aquifer near Roswell are known to be
high. A significant source of the nitrates
comes from surrounding dairy farms
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(Sarah McGrath, New Mexico State
Ground Water Bureau, pers. comm.
2001). The effects of nitrates on aquatic
species are not entirely known because
several outcomes may result from highlevel nitrate contamination in aquatic
systems. One outcome includes
increased growth of algae resulting from
increased nutrients in the aquatic
system. Too much algae in an aquatic
environment could result in periods of
low dissolved oxygen and in extreme
cases this could be lethal to the snails
and the amphipod. At least two dairy
farms are currently required to do
remediation for their contribution of
nitrates to water pollution, both surface
and underground (Sarah McGrath, New
Mexico State Ground Water Bureau,
pers. comm. 2001).
Oil and Gas Operations
Oil drilling occurs throughout the
Roswell Basin. This activity and
associated actions can threaten the
water quality of the aquifer on which
these species depend. For example, oil
and other contaminants from drilling
activities throughout the basin could
enter the aquifer supplying the springs
inhabited by all four species when the
limestone layers are pierced by drilling
activities.
There are 196 natural gas and oil
wells in the 12-township area
encompassing the source-water capture
zone for the Middle Area of BLNWR
that are potential sources of
contamination (New Mexico Petroleum
Research Center 2002). Of these, 17 oil
and gas leases are currently within the
habitat protection zone, which
encompasses 12,585 ac (5,093 ha) of
Federal mineral estate within the water
resource area for BLNWR (Service
2005a). A total of 20 natural gas wells
currently exist on these leases. BLM has
estimated a maximum potential
development of 66 additional wells
within the habitat protection zone,
according to well spacing requirements
established by the New Mexico Oil
Conservation Division. 48 (Service
2005a). There were 200 (59 on State, 33
on Private, and 108 on Federal lands)
‘‘intentions to drill’’ (pursuit of required
permits has been initiated by an
applicant) filed for oil or natural gas on
Federal lands in Chavez County, from
2002 through the last update in June
2004 (Go-Tech 2005).
There are numerous examples in
which oil and gas operations have
employed regulatory standards within
the karst lands of the Permian Basin in
New Mexico and other states, but these
measures failed to protect groundwater
resources and aquifer drawdown
(NMISC 2002). To remediate (clean) the
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aquifer would be extremely difficult
should it become contaminated by oil,
chemicals, or organics such as nitrates.
In most cases contamination of an
underground aquifer by agricultural,
industrial, or domestic sources is treated
at the source. When a contamination
site is discovered, techniques are used
to address the source of the
contamination. Rarely do remediation
efforts pump water from the aquifer and
treat it before sending it back. This is
largely because these techniques are
very costly and difficult to apply (Sarah
McGrath, New Mexico State Ground
Water Bureau, pers. comm. 2001).
Because these invertebrate species are
sensitive to contaminants, efforts to
clean up pollution source sites after the
aquifer has been contaminated may not
be sufficient to protect these species and
the aquatic habitat on which they
depend.
Operations associated with oil and gas
drilling such as exploration, storage,
transfer, and refining are also potential
threats to these species (Jercinovic 1982,
1984; Longmire 1983; Quarles 1983;
Boyer 1986; Green and Trett 1989;
Service 1997). Such extractive processes
and industry operations are known to
contaminate ground and surface waters
(Jercinovic 1982, 1984; Longmire 1983;
Quarles 1983; Boyer 1986; Richard
1988a, 1988b; Rail 1989; Richard and
Boehm 1989a, 1989b; Jones and Balleau
1996). Moreover, large volumes of water
(about 12 billion gallons (39,000 acre
feet) in 1985) are produced concurrently
with oil and gas extraction, especially in
southeastern New Mexico (Boyer 1986).
For example, in southeastern New
Mexico, the average water-to-oil ratio
produced in 1985 was 4.5 to 1 (Boyer
1986). This water may be injected into
the ground in some areas to recover
more oil, but can also be disposed of in
permitted surface pits (Boyer 1986).
This groundwater depletion and ground
and surface water contamination can
adversely impact aquatic mollusks
(Eisler 1987, Green and Trett 1989) and
threaten Roswell springsnail, Koster’s
springsnail, Pecos assiminea, and Noel’s
amphipod populations at BLNWR
(Service 1997).
Oil and gas activities also threaten the
Pecos assiminea because of the potential
groundwater or surface water
contamination from pollutants (Veni
1991). The Diamond Y Springs Complex
is within an active oil and gas extraction
field. At this time there are still many
active wells and pipelines located
within a hundred meters of surface
waters. In addition, a natural gas
refinery is located within 0.8 km (0.5
mi) upstream of Diamond Y Spring.
There are also old brine pits associated
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with previous drilling within feet of
surface waters. Oil and gas pipelines
cross the spring outflow channels and
marshes where the species occurs,
creating a constant potential for
contamination from pollutants from
leaks or spills. These activities pose a
threat to the habitat of the Pecos
assiminea by creating the potential for
pollutants to enter underground aquifers
that contribute to spring flow or by
point sources from spills and leaks of
petroleum products on the surface.
As an example of this threat, in 1992
approximately 10,600 barrels of crude
oil were released from a 6-in (15.2 cm)
pipeline that traverses Leon Creek above
its confluence with Diamond Y Draw.
The oil was from a ruptured pipeline at
a point several hundred feet away from
the Leon Creek channel. The site itself
is about 1 mile (1.6 km) overland from
Diamond Y Spring. The distance that
surface runoff of oil residues must travel
is about 2 miles (3.2) down Leon Creek
to reach Diamond Y Draw. The pipeline
was operated at the time of the spill by
the Texas-New Mexico Pipeline
Company, but ownership has since been
transferred to several other companies.
Texas Railroad Commission has been
responsible for overseeing cleanup of
the spill site. Remediation of the site
initially involved aboveground land
farming of contaminated soil and rock
strata to allow microbial degradation. In
recent years, remediation efforts have
focused on vacuuming oil residues from
the surface of groundwater exposed by
trenches dug at the spill site. To date,
no impacts on the rare fauna of
Diamond Y Springs Complex have been
observed, but no specific monitoring of
the effects of the spill was undertaken
(Service 2005b).
B. Overutilization for commercial,
recreational, scientific, or educational
purposes. Roswell springsnail, Koster’s
springsnail, Pecos assiminea, and Noel’s
amphipod may occasionally be
collected as specimens for scientific
study, but these uses probably have a
negligible effect on total population
numbers. These species are currently
not known to be of commercial value,
and overutilization has not been
documented. However, as their rarity
becomes known, they may become more
attractive to collectors. Although
scientific collecting is not presently
identified as a threat, unregulated
collecting by private and institutional
collectors could pose a threat to these
locally restricted populations. We are
aware of overcollection being a potential
threat with other snails (e.g., armored
snail (Pyrgulopsis (Marstonia) pachyta)
(65 FR 10033, February 25, 2000);
Bruneau hot springsnail (P.
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bruneauensis) (58 FR 5938, January 25,
1993); and Socorro springsnail (P.
neomexicana) and Alamosa springsnail
(Tryonia alamosae) (56 FR 49646,
September 30, 1991)), due to their rarity,
restricted distribution, and generally
well known locations. Due to the small
number of localities for the snails and
the amphipod, these species are
vulnerable to unrestricted collection,
vandalism, or other disturbance. There
is no documentation of collection as a
significant threat to any of the species.
Therefore, we believe that collection of
the animals is a minor but present
threat.
C. Disease or predation. Springsnails
and amphipods are a food source for
other aquatic animals. Juvenile
springsnails appear vulnerable to a
variety of predators. Damselflies
(Zygoptera) and dragonflies (Anisoptera)
were observed feeding upon snails in
the wild (Mladenka 1992). Damselflies
and dragonflies are native to and
abundant at BLNWR and most likely
prey upon both the springsnails and
Noel’s amphipod.
Springsnails are vulnerable to
predation by fish (Kennedy 1977;
Winemiller and Anderson 1997).
Mladenka (1992) observed guppies
feeding on springsnails in the
laboratory. The non-native fish present
at BLNWR (carp and mosquitofish) most
likely also prey upon the springsnails
and Noel’s amphipod when they occur
in the same habitats. The extent to
which predation from non-native fish
affects population size of the three
aquatic invertebrates is not known.
Predation pressure on Pecos assiminea
is also unknown. However, if the land
snail Rumina becomes established at
BLNWR, the potential exists for it to
predate on Pecos assiminea.
Infestation by trematodes (a flatworm
or fluke, phylum Platyhelminthes) was
noted by Taylor (1987) in populations of
Koster’s springsnail at Sago Spring,
BLNWR. Digenetic trematodes
(trematodes in the order Digenera) are
parasitic and have the most complicated
life histories in the animal kingdom
involving two to four intermediate
(vertebrate and/or invertebrate) hosts
(Hickman et al. 1974). The first larval
stage of the trematode nearly always
uses a mollusk (snail or bivalve) as the
first intermediate host (Hickman et al.
1974). Larval trematode parasites reduce
or completely inhibit snail reproduction
through castration (Minchella et al.
1985). The effect of the trematodes on
the springsnail population is not
known.
The terrestrial land snail (Rumina
decollate) was introduced to the United
States in the early 1800s in South
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Carolina and spread westward (Selander
and Kaufman 1973). It was reported in
Arizona in 1952 and California in 1966
but was well-established by the time it
was discovered (Selander and Kaufman
1973). It is common in Texas (Selander
and Kaufman 1973) and has been
reported from the Roswell area in New
Mexico (Lang 2005b). It inhabits gardens
and agricultural areas but has also
invaded riparian and other native
habitats (Selander and Kaufman 1973).
It is used in California as a biological
control agent against the brown garden
snail (Helix aspera) (Cowie 2001). It will
consume native snails (Cowie 2001) as
well as vegetation (Dundee 1984). For
these reasons, Rumnia is a potential
threat to Pecos assiminea.
Non-native aquatic species such as
crayfish, fish, and aquatic snails are also
a potential threat to the four
invertebrates. There is only one species
of crayfish native to New Mexico, but its
distribution does not overlap with that
of the four invertebrates (Hobbs 1991).
Crayfish are typically opportunistic
generalists (they will eat anything and
everything) (Hobbs 1991). Predation on
invertebrates is well-documented
(Hobbs 1991; Lodge et al. 1994;
Charlebois and Lamberti 1996; Strayer
1999). However, because they also feed
on organic debris and vegetation and
reduce algal biomass (Charlebois and
Lamberti 1996), they could potentially
compete with Roswell springsnail,
Koster’s springsnail, and Noel’s
amphipod for food resources. Currently
non-native crayfish are not present at
BLNWR or the sites in Texas. Diamond
Y Springs Complex does have an
undescribed native crayfish which we
do not believe to be a concern for Pecos
assiminea. However, crayfish have
created major problems in aquatic
systems in Arizona, and there is no
physiological reason why some species
of crayfish could not survive in the
habitats that now support the four
invertebrates. Eradication of crayfish
once they are established is extremely
difficult (Hyatt 2004). Diamond Y
Springs Complex has an undescribed
native crayfish which we do not believe
to be a concern for Pecos assiminea.
Non-native fish have had a major
impact on native aquatic fauna in the
Southwest (Minckley and Douglas 1991;
Desert Fishes Team 2003). Communities
of animals evolved together and
developed adaptations to deal with
competition and predation from other
members of the community (Meffe et al.
1994). When a non-native species is
introduced into this community the
native members often do not have
defenses against predation or they may
be less successful competitors. As a
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result, the non-native species can have
a major impact on native populations
(Minckley and Douglas 1991; Meffe et
al. 1994). One species of non-native
fish, common carp (Cyprinus carpio), is
known to co-occur with the three
aquatic invertebrates at BLNWR. Native
to Asia, common carp was introduced
into the United States in 1831, has
become widely distributed (Sublette et
al. 1990), and is present at BLNWR in
habitats occupied by the invertebrates.
Through spawning and feeding behavior
it uproots vegetation and increases
turbidity (Sublette et al. 1990). It is an
omnivore feeding on aquatic
invertebrates, fish eggs, algae, plants,
and organic matter (Sublette et al. 1990).
Because of its non-discriminatory diet
and habitat disturbance, it could have
an impact on the three aquatic
invertebrate species.
Mosquitofish (Gambusia affinis) is
also present in some of the spring
systems at BLNWR, but it is not known
if it is native to the area or not. The
species is native to portions of New
Mexico but it has also been widely
introduced to control mosquitoes
(Sublette et al. 1990). However, it has
negatively affected or extirpated many
species of fish and invertebrates (e.g.,
through predation) (Meffe et al. 1994). It
is not known if mosquitofish are
affecting the three species of aquatic
invertebrates.
Non-native mollusks have affected the
distribution and abundance of native
mollusks in the United States. Of
particular concern for three of the
invertebrates (Noel’s amphipod, Roswell
springsnail, and Koster’s springsnail)
are Melanoides tuberculata (red-rim
melania) and Potamopyrgus
antipodarum (New Zealand mudsnail).
Both of these snails are excellent
colonizers that reach tremendous
population sizes and have been found in
isolated springs in the West. Melanoides
has caused the decline and local
extirpation of native snail species, and
it is considered a threat to endemic
aquatic snails that occupy springs and
streams in the Bonneville Basin of Utah
(Rader et al. 2003). It is easily
transported on gear or aquatic plants,
and because it reproduces asexually
(individuals can develop from
unfertilized eggs), a single individual is
capable of founding a new population.
It has become established in isolated
desert spring ecosystems such as Ash
Meadows, Nevada, and Cuatro Cinegas,
Mexico, and within the last 10 years,
Melanoides has become established in
Diamond Y Springs Complex (Echelle
2001; McDermott 2000). It has become
the most abundant snail in the upper
watercourse of the Diamond Y Springs
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Complex (Echelle 2001). In many
locations, this exotic snail is so
numerous that it essentially is the
substrate in the small stream channel.
The effect Melanoides is having on
native snails is not known; however,
because it is aquatic it probably has less
effect on Pecos assiminea than on the
other endemic aquatic snails present in
the spring.
Potampyrgus is also a potential threat
to the endemic aquatic snails at BLNWR
and the spring systems in Texas. It was
discovered in the Snake River, Idaho, in
the mid-1980s and has quickly spread to
every Western state except New Mexico
(Montana State University https://
www.esg.montana.edu/aim/mollusca/
nzms/status.html, accessed on June 16,
2005). Like Melanoides, Potamopyrgus
has an operculum (a lid to close off the
shell opening), can withstand periods of
drying up to 8 days (thereby facilitating
transport) and can reproduce either
sexually or asexually. Thus, new
populations can be established with
transport of a single individual. In
addition, Potampyrgus is tiny (3 mm in
height [0.12 in]), is easily overlooked on
gear or shoes, and can be transported
unknowingly by people visiting various
recreational sites. Considering its
current rate of expansion, and the
availability of suitable habitat, it is
highly likely that Potampyrgus will
soon be discovered in New Mexico.
Potampyrgus tolerates a wide range of
habitats, including brackish water.
Densities are usually highest in systems
with high primary productivity,
constant temperatures, and constant
flow (typical of spring systems). It has
reached densities exceeding 500,000 m2
(Richards et al. 2001) to the detriment
of native invertebrates. Not only can it
dominate the invertebrate assemblage
(97 percent of invertebrate biomass), it
can also eat nearly all of the algae and
diatoms growing on the substrate,
altering ecosystem function at the base
of the food web (food is no longer
available for native animals) (Hall et al.
2003). If Potampyrgus is introduced into
the spring systems harboring the
proposed invertebrates, control would
most likely be impossible because the
snails are so small and because any
chemical treatment would also affect the
native species. The impact could be
devastating.
D. The inadequacy of existing
regulatory mechanisms. One primary
cause of decline of the Roswell
springsnail, Koster’s springsnail, Pecos
assiminea, and Noel’s amphipod is the
loss, degradation, and fragmentation of
habitat due to human activities. Federal
and State laws have been insufficient to
prevent past and ongoing losses of the
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limited habitat of the four invertebrates,
and are unlikely to prevent further
declines of the species.
Federal
Clean Water Act. Pursuant to section
404 of the Clean Water Act (CWA) (33
U.S.C. 1344), the U.S. Army Corps of
Engineers (Corps) regulates the
discharge of dredged or fill material into
all Waters of the United States,
including wetlands. In general, the term
‘‘’wetland’’’ refers to areas meeting the
Corps criteria of having hydric soils,
hydrology (either a defined minimum
duration of continuous inundation or
saturation of soil during the growing
season), and a plant community that is
predominantly hydrophytic vegetation
(plants specifically adapted for growing
in a wetland environment). The spring
complexes occupied by these four
invertebrates qualify as wetlands.
Any discharge of dredged or fill
material into waters of the United
States, including wetlands, requires a
permit from the Corps. These include
individual permits which would be
issued following a review of an
individual application, and general
permits that authorize a category or
categories of activities in a specific
geographical location or nationwide (33
CFR parts 320–330). General and special
permit conditions may vary among
individual Corps Districts and the
various general permits. However, the
use of any individual or general permit
requires compliance with the Act.
While the CWA provides a means for
the Corps to regulate the discharge of
dredged or fill material into waters and
wetlands of the United States, it does
not provide complete protection. Many
applicants are required to provide
compensation for wetlands losses (i.e.,
no net loss) and many smaller impact
projects remain largely unmitigated
unless specifically required by other
environmental laws such as the Act.
Moreover, we are not aware of any
Corps permits that have been issued for
the spring complexes where these
species occur or historically occurred,
indicating that there is little protection
provided to these species through the
CWA.
Recent court cases limit the Corps’
ability to utilize the CWA to regulate the
discharge of fill or dredged material into
the aquatic environment within the
current range of the Roswell springsnail,
Koster’s springsnail, Pecos assiminea,
and Noel’s amphipod (Solid Waste
Agency of Northern Cook County v. U.S.
Army Corps of Engineers, 531 U.S. 159
(2001) (SWANCC)). There may be
instances where seasonal wetlands used
by California tiger salamander lack
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sufficient connection to waters of the
United States for the Corps to assert
jurisdiction under the authority of the
Clean Water Act. For example, the
Corps frequently cites the SWANCC
decision as their reason for not taking
jurisdiction over waterbodies that do
not meet the definition of waters of the
United States. For these reasons, we
conclude that regulation of wetlands
filling by the Corps under Section 404
of the CWA is inadequate to protect the
Roswell springsnail, Koster’s
springsnail, Pecos assiminea, and Noel’s
amphipod from further decline.
Revisions to the Roswell Approved
Resource Management Plan made by
BLM in 1997 prompted a formal section
7 consultation with the Service
regarding the endangered Pecos
gambusia (Gambusia nobilis), which
resides on BLNWR. The BLM
designated an area for protection of
habitat for Pecos gambusia from
potential groundwater contamination by
oil and gas well drilling operations
(BLM 2002). This area, referred to as the
Habitat Protection Zone (HPZ), includes
a portion of the source-water capture
area for the springs in the northern part
of the Middle Tract of BLNWR, where
Pecos gambusia co-occurs with the four
invertebrate species. The HPZ includes
12,585 ac (5,093 ha) of the Federal
mineral estate and 9,945 ac (4,025 ha) of
the Federal surface estate that are within
the water source area for the BLNWR.
The HPZ was established in October of
2002 and special requirements for oil
and gas well development managed to
protect the ground and surface water
resources (BLM 2002). For example,
stipulations for oil and gas wells in the
HPZ include storage of drilling muds in
steel tanks and use of cement to seal the
entire length of the well casing. These
requirements reduce the probability of
contamination from oil and gas
development but do not reduce the
likelihood of groundwater
contamination attributable to oil and gas
storage or transportation activities (e.g.
leaking pipelines, storage tanks, or other
equipment failures). Therefore, the HPZ
does not eliminate the threat of oil and
gas activities on these species, nor does
it address the other threats identified
under Factor A (e.g., drought, septic
tank leaching, etc).
State
Existing New Mexico State regulatory
mechanisms are inadequate to protect
the Roswell springsnail, Koster’s
springsnail, Pecos assiminea, and Noel’s
amphipod. All four species are listed as
New Mexico State endangered species,
Group 1, which are those species
‘‘whose prospects of survival or
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recruitment within the State are in
jeopardy.’’ This designation provides
the protection of the New Mexico
Wildlife Conservation Act, but only
prohibits direct take of these species,
except under issuance of a scientific
collecting permit. New Mexico State
statutes do not address habitat
protection, indirect effects, or other
threats to these species. New Mexico
State status as an endangered species
only conveys protection from collection
or intentional harm. However, there is
no formal consultation process to
address the habitat requirements of the
species or how a proposed action may
affect the needs of the species. Because
most of the threats to these species are
from effects to habitat, protecting
individuals will not ensure their longterm protection.
NMDGF recognizes the importance of
Roswell springsnail, Koster’s
springsnail, Pecos assiminea, and Noel’s
amphipod conservation at the local
population level and has the authority
to consider and recommend actions to
mitigate potential adverse effects to
these species during its review of
development proposals. As noted,
NMDGF’s primary regulatory venue is
under the New Mexico Wildlife
Conservation Act. There are no statutory
requirements under NMDGF’s
jurisdiction that serve as an effective
regulatory mechanism for reducing or
eliminating the threats (see Factors A
and C above) that may adversely affect
Roswell springsnail, Koster’s
springsnail, Pecos assiminea and their
habitat.
Still, New Mexico State statutes
require the NMDGF to develop a
recovery plan that will restore and
maintain species’ habitat. A recovery
and conservation plan for the four
invertebrates was finalized by the State
of New Mexico in January 2005
(NMDGF 2005b). The plan provides
details about the natural history of the
invertebrates, a historical perspective of
habitat and population trends, and
habitat assessment. The goal of the plan
is to ensure that the invertebrates occur
in sufficient numbers within
populations and in a sufficient number
of discrete and independent
populations, that downlisting and
eventual delisting under the Wildlife
Conservation Act is warranted (NMDGF
2005b). The plan outlines three
parameters to meet the goal: (1)
Maintenance or expansion of the
existing distribution and abundance of
the invertebrates at BLNWR; (2)
repatriation of the invertebrates to
restored suitable habitat at two or more
sites within their known historic range;
and (3) establishment and stocking of an
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artificial and secure refugium to protect
against catastrophic loss in the wild
(NMDGF 2005b). As noted above, the
State’s recovery plan does not ensure
any long-term protection for these
species because there are no mandatory
elements to ensure proposed projects do
not adversely affect these species or
their habitat.
The Oil Conservation Division of the
New Mexico Energy, Minerals, and
Natural Resources Department regulates
oil and gas well drilling and casing in
part to prevent contamination of
groundwater (19 NMAC 15.3). Although
there are no known instances of
groundwater contamination by leaking
oil or gas wells in the source-water
capture zone for the Middle Unit of
BLNWR, there is a well documented
history of oil and gas industry
operations on and adjacent to BLNWR,
which have resulted in the spillage of
oil and brine onto the BLNWR (Service
1994b, 1996, 1997a, 1998b). Therefore,
we find that these regulations provide
some protection to the four
invertebrates, but do not eliminate the
threat of oil spills through accidents or
equipment malfunctions.
The environmental assessment found
that spring flows within the proposed
critical habitat on BLNWR are already
protected by existing water rights
afforded by the New Mexico Office of
the State Engineer’s administration of
the Roswell Basin. In 1967, water rights
were adjudicated in the Roswell Basin,
wells were metered, and pumping rates
administered by the Office of the State
Engineer (OSE). Currently, any
proposed change in use of water
(underground or surface depletion) in
the Roswell Basin will undergo analysis
by OSE to determine if there would be
impairment to existing water rights
(McCord et al. 2005). The OSE will not
allow such change if it impairs the
Federal water right in any respect
(NMISC 2005). Thus the spring flows on
BLNWR should be protected from any
changes in groundwater pumping near
the refuge in the future. This provides
a regulatory benefit to the four
invertebrates.
However, we believe that there was a
lag between the time of the drought and
recovery in the artesian groundwater in
this area. Because New Mexico has been
in a drought since 1999, there may be
a lag time before the effect of the current
drought is observed. We believe that the
springs on BLNWR will flow in spite of
relatively intense drought (McCord et al.
2005). However, it is not known how
the springs in Texas would respond to
extended drought and the current level
of groundwater pumping. Moreover, the
habitat occupied by the four
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invertebrates does not have to dry out
completely to have an effect on
populations. Lower spring flows may
cause a decrease in habitat availability,
increased water temperatures, lower
dissolved oxygen levels, and an increase
in salinity (MacRae et al. 2001). Any of
these factors, alone or in combination,
could lead either to the reduction or
extirpation of a population.
Additionally, the primary threat to
Pecos assiminea in Texas is the
potential failure of spring flow due to
excessive groundwater pumping and/or
drought, which would result in total
habitat loss for the species.
In Texas, Pecos assiminea currently
has no State or other regulatory
protection. Some protection for the
habitat of this species is provided with
the ownership of the springs by TNC
(Karges 2003). However, this land
ownership provides no protection from
one of the main threats to this species—
the loss of necessary groundwater levels
to ensure adequate spring flows.
Groundwater pumping that could affect
spring flows is subject to limited
regulation in Texas. State agencies do
not control groundwater pumping, and
Texas courts have held that, with few
exceptions, landowners have the right to
take all the water that can be captured
under their land (rule of capture),
regardless of impacts to neighbors or
natural resources. Individual
groundwater conservation districts have
varying amounts of authority and
capacity to limit pumping. Diamond Y
Spring is within the jurisdiction of the
Middle Pecos Groundwater
Conservation District, but generally
groundwater districts will not limit
groundwater use to allow for
conservation of surface water flows
(Booth and Richard-Crow 2004; Caroom
and Maxwell 2004). Thus, we find no
existing regulatory mechanisms in place
to protect the Pecos assiminea.
Members of the four invertebrate
species that co-exist in springs with the
federally endangered Pecos gambusia
(Gambusia nobilis) at BLNWR and
Diamond Y Spring and the federally
endangered Leon Springs pupfish at
Diamond Y Spring may receive
incidental habitat protection from the
Act. However, possible habitat
protection provided by the federally
listed Pecos gambusia and the Leon
Springs pupfish offers only partial
protection for the Roswell springsnail,
Koster’s springsnail, Pecos assiminea,
and Noel’s amphipod because the
federally listed fish are not found in all
the springs the snails or amphipod
inhabit. For example, Pecos assiminea
does not normally occur directly within
submerged habitats. It is most
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commonly found in moist soil or
vegetation along the periphery of
standing water. As a result, this habitat
may not be afforded protection under
current management actions or
consultations which address
conservation for listed fish species in
the same area.
Federal water-rights for the BLNWR
were secured in 1996 (Service 2005b).
This acquisition should ensure
minimum surface water discharge of
Bitter Creek. However, if this water is
contaminated, the Federal water right
alone does not provide adequate
protection for these species.
E. Other natural or manmade factors
affecting its continued existence.
BLNWR was established in 1937 as
wintering and breeding grounds for
migratory birds. At the time the four
invertebrates were unknown to science.
Consequently, management was
directed primarily at creating dikes so
that ponds could be created and their
water levels controlled for the benefit of
waterfowl. Some of the ponds created
would seasonally flood springs that
flowed into these ponds naturally.
Because the Roswell springsnail and
Noel’s amphipod, in particular, prefer
flowing over pooled water, this had a
negative impact on the habitat available
to them. In 2003, a dike rehabilitation
project was begun on BLNWR. Two
dikes running the length of Areas 6 and
7 were constructed. This isolated the
spring systems from the main body of
the impoundments, allowing the areas
to be flooded in the winter without
inundating the springs occupied by the
invertebrates. In addition, potential
habitat for the invertebrates was created
in a new ditch designed to carry water
to Area 7. Current management of
BLNWR recognizes and includes the
invertebrates in its maintenance and
operations, and is no longer a threat to
the invertebrates.
Fire
BLNWR is characterized by sinkhole/
karst terrain. This terrain poses safety
threats to fire crews and suppression
equipment. As a result, fire suppression
efforts are largely restricted to
established roads. This severely limits
management ability to quickly suppress
fires that threaten fragile aquatic
habitats on the BLNWR. On March 5,
2000, the Sandhill fire burned 405 ha
(1,000 ac) of the western portion of the
BLNWR, including portions of Bitter
Creek. The fire burned through
Dragonfly Spring, eliminated vegetation
shading the spring, and generated a
substantial amount of ash in the spring
system (Lang 2000, NMDGF 2005b,
2005c). Subsequently, dense algal mats
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formed, water temperature fluctuations
and maximum temperatures increased,
while dissolved oxygen levels decreased
(Lang 2002). The pre-fire dominant
vegetation of submerged aquatic plants
and mixed native grasses within the
burned area has also been replaced by
the invasive common reed (NMDGF
2005b, 2005c). Following the fire, a
dramatic reduction in Noel’s amphipod
was observed, and Koster’s springsnail
occurs at lower densities than were
observed prior to the fire (Lang 2002,
NMDGF 2005c).
Currently, dense stands of common
reed are found throughout most reaches
of Bitter Creek, including in habitat
occupied by the four invertebrates
(NMDGF 2005c) (see also ‘‘Factor C’’
section above). Prior to the Sandhill
Fire, common reed occurred only
sporadically along Bitter Creek (NMDGF
2005c). These dense stands of common
reed have increased the fuel load and
threat of wildfire on BLNWR. Standing
dead canes of common reed and
associated litter often constitute twice as
much biomass as living shoots (Uchytil
1992). This abundant dead fuel carries
fire well, allowing stands to burn even
when the current year’s shoots are green
(Uchytil 1992). Because of the increase
in common reed on BLNWR within
habitat occupied by the four
invertebrates, we now find that wildfire
is a threat to the four invertebrates.
Removal of vegetative cover by
burning in habitats occupied by Pecos
assiminea may be an important factor in
decline or loss of populations (Taylor
1987). Alternatively, Pecos assiminea
has been found to persist in areas
following fires (Lang 2000). Pecos
assiminea was also discovered at
Dragonfly Spring following burning of
habitat there during the Sandhill Fire
(NMDGF 2005a). Season of burning,
intensity of the fire, and frequency of
fire are likely important determinants of
effects on population persistence and
abundance of Pecos assiminea (NMDGF
1998). Pecos assiminea is potentially
more vulnerable to fires than the
springsnails because they reside at or
near the surface of the water. However,
it is thought that Pecos assiminea may
survive fire or other vegetation
reduction if sufficient litter and ground
cover remain to sustain appropriate soil
moisture and humidity at a microhabitat
scale (NMDGF 2005a; Service 2004).
Controlled burns have been
implemented on BLNWR to burn grass,
sedge, cattail, and non-native vegetation
(e.g., Russian thistle) in an attempt to
reduce the risk of large uncontrolled
wildfires or to remove excessive
amounts of Russian thistle from a spring
run (Service 2004). We have found that
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controlled burns with appropriate
conservation measures do not adversely
affect the Koster’s springsnail, Pecos
assiminea, or Roswell springsnail
(Service 2004). On the other hand,
prescribed burns to remove Russian
thistle may have indirectly affected
Noel’s amphipod through the release of
common reeds, which can reduce water
flow and result in decreased dissolved
oxygen levels (Service 2005c). Surveys
conducted immediately post-fire
indicate that Noel’s amphipod is still
found throughout the burned area, with
little to no direct effects (Service 2005c).
Still, the Service is continuing to
monitor post-fire effects from these
activities to determine if Noel’s
amphipod has been adversely affected.
Fire, particularly during the winter
months, will allow ash, sediment, salts,
and nutrients to more readily enter the
aquatic habitat via precipitation and
wind. Ash consists of carbon, soots, and
other organic compounds that, upon
entering the water column, provide a
food source for bacteria and algae. With
the addition of associated nutrients, and
water temperature increases from the
loss of streamside vegetation,
populations of bacteria and algae will
expand, causing oxygen depletions. As
a result, some invertebrates may perish
in these situations, where they cannot
escape the oxygen deficit. Additionally,
denuded areas will allow erosion and
sedimentation of the streamside habitat.
Sedimentation could have the direct
effect on the Roswell springsnail, which
is typically found on rocks.
Finding
We have carefully assessed the best
scientific and commercial information
available regarding the past, present,
and future threats faced by these species
in determining that these species are in
danger of extinction throughout all or a
significant portion of their respective
ranges. The habitat and range of Roswell
springsnail, Koster’s springsnail, Pecos
assiminea, and Noel’s amphipod are
threatened with destruction,
modification, and curtailment. Existing
regulatory mechanisms do not provide
adequate protection for these species,
and other natural and manmade factors
affect their continued existence.
Because each of these four species has
a very limited range, their populations
are disjunct and isolated from each
other, and potential habitat areas are
isolated and separated by large areas of
unsuitable habitat, these invertebrates
are particularly vulnerable to localized
extinction should their habitat be
degraded or destroyed. Because their
mobility is limited, populations will
have little opportunity to leave
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degraded habitat areas in search of
suitable habitat. As a result, one
contamination event, or a short period
of drawdown in the aquatic habitat
where they are found could result in the
loss of an entire population, of which
there are few. Because of the limited
distribution of these endemic species,
any impact from increasing threats (e.g.,
loss of springflow, contaminants,
nonnative species) is likely to result in
their extinction because the magnitude
of threat is high. These species occur in
an arid region plagued by drought and
ongoing aquifer withdrawals (e.g., in
Texas), making the loss of springflows
an imminent threat in the foreseeable
future. We also found that their habitat
faces a constant threat from water
quality contamination. Therefore, we
have determined that the Roswell
springsnail, Koster’s springsnail, Pecos
assiminea, and Noel’s amphipod meet
the definition of an endangered species
pursuant to section 3 of the Act. A
threatened species designation as
defined in section 3 of the Act would
not accurately reflect the population
status, restricted distribution,
vulnerability, and imminent threats. As
such, we are listing these four
invertebrate species as endangered
under the Act.
Critical Habitat
Designation of Critical Habitat Provides
Little Additional Protection to Species
In 30 years of implementing the Act,
the Service has found that the
designation of statutory critical habitat
provides little additional protection to
most listed species, while consuming
significant amounts of conservation
resources. The Service’s present system
for designating critical habitat is driven
by litigation rather than biology, limits
our ability to fully evaluate the science
involved, consumes enormous agency
resources, and imposes huge social and
economic costs. The Service believes
that additional agency discretion would
allow our focus to return to those
actions that provide the greatest benefit
to the species most in need of
protection.
Role of Critical Habitat in Actual
Practice of Administering and
Implementing the Act
While attention to and protection of
habitat is paramount to successful
conservation actions, we have
consistently found that, in most
circumstances, the designation of
critical habitat is of little additional
value for most listed species, yet it
consumes large amounts of conservation
resources. Sidle (1987) stated, ‘‘Because
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the Act can protect species with and
without critical habitat designation,
critical habitat designation may be
redundant to the other consultation
requirements of section 7.’’
Currently, only 445 species, or 36
percent, of the 1,244 listed species in
the United States under the jurisdiction
of the Service have designated critical
habitat. We address the habitat needs of
all 1,244 listed species through
conservation mechanisms such as
listing, section 7 consultations, the
Section 4 recovery planning process, the
section 9 protective prohibitions of
unauthorized take, section 6 funding to
the States, and the section 10 incidental
take permit process. The Service
believes that it is these measures that
may make the difference between
extinction and survival for many
species.
We note, however, that a recent 9th
Circuit judicial opinion, Gifford Pinchot
Task Force v. United States Fish and
Wildlife Service, has invalidated the
Service’s regulation defining destruction
or adverse modification of critical
habitat. We are currently reviewing the
decision to determine what effect it may
have on the outcome of consultations
pursuant to section 7 of the Act.
Procedural and Resource Difficulties in
Designating Critical Habitat
We have been inundated with
lawsuits regarding critical habitat
designation, and we face a growing
number of lawsuits challenging critical
habitat determinations once they are
made. These lawsuits have subjected the
Service to an ever-increasing series of
court orders and court-approved
settlement agreements, compliance with
which now consumes nearly the entire
listing program budget. This leaves the
Service with little ability to prioritize its
activities to direct scarce listing
resources to the listing program actions
with the most biologically urgent
species conservation needs.
The consequence of the critical
habitat litigation activity is that limited
listing funds are used to defend active
lawsuits and to comply with the
growing number of adverse court orders.
As a result, the Service’s own proposals
to undertake conservation actions based
on biological priorities are significantly
delayed.
The accelerated schedules of court
ordered designations have left the
Service with almost no ability to
provide for meaningful additional
public participation beyond those
minimally required by the
Administrative Procedure Act (APA),
the Act, and the Service’s implementing
regulations, or to take additional time
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for review of comments and information
to ensure the rule has addressed all the
pertinent issues before making decisions
on listing and critical habitat proposals,
due to the risks associated with
noncompliance with judicially imposed
deadlines. This in turn fosters a second
round of litigation in which those who
will suffer adverse impacts from these
decisions challenge them. The cycle of
litigation appears endless, is very
expensive, and in the final analysis
provides little additional protection to
listed species.
The costs resulting from the
designation include legal costs, the cost
of preparation and publication of the
designation, the analysis of the
economic effects and the cost of
requesting and responding to public
comment, and in some cases the costs
of compliance with the NEPA; all are
part of the cost of critical habitat
designation. These costs result in
minimal benefits to the species that are
not already afforded by the protections
of the Act enumerated earlier, and they
directly reduce the funds available for
direct and tangible conservation actions.
Section 3(5)(A) of the Act defines
critical habitat as the specific areas
within the geographical area occupied
by the species on which are found those
physical and biological features (I)
essential to the conservation of the
species and (II) which may require
special management considerations or
protection and that the designation of
critical habitat for a given species is
prudent and determinable.
‘‘Conservation’’ means the use of all
methods and procedures that are
necessary to bring an endangered or a
threatened species to the point at which
listing under the Act is no longer
necessary. Because we proposed critical
habitat for the four invertebrates, we
already determined that critical habitat
pursuant to the Act and implementing
regulations was both prudent and
determinable (67 FR 6459).
Section 3(5)(c) of the Act states that
not all areas that can be occupied by a
species should be designated as critical
habitat unless the Secretary determines
that all such areas are essential to the
conservation of the species. Our
regulations (50 CFR 424.12(e)) also state
that ‘‘The Secretary shall designate as
critical habitat areas outside the
geographical area presently occupied by
the species only when a designation
limited to its present range would be
inadequate to ensure the conservation of
the species.’’
Areas within the geographical area
occupied by the species that do not
contain the features essential for the
conservation of the species are not, by
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definition, critical habitat. Similarly,
within the geographical area occupied
by the species, if the features essential
for the conservation of the species will
not require special management
considerations or protection, the area is
not, by definition, critical habitat. To
determine whether the essential features
within an area may require special
management, we first determine if the
essential features located there generally
require special management to address
applicable threats. If those features do
not require special management, or if
they do in general but not for the
particular area in question because of
the existence of an adequate
management plan or for some other
reason, then the essential features
within the area do not require special
management.
Further, section 4(b)(2) of the Act
states that critical habitat shall be
designated, and revised, on the basis of
the best available scientific data after
taking into consideration the economic
impact, impact on national security, and
any other relevant impact of specifying
a particular area as critical habitat. An
area may be excluded from critical
habitat if it is determined that the
benefits of exclusion outweigh the
benefits of specifying a particular area
as critical habitat, unless the failure to
designate such area as critical habitat
will result in the extinction of the
species.
The designation of critical habitat
does not affect land ownership or
establish a refuge, wilderness, reserve,
preserve, or other conservation area. It
does not allow government or public
access to private lands. Under section 7
of the Act, Federal agencies must
consult with the Service on activities
they undertake, fund, or permit that
may affect critical habitat and lead to its
destruction or adverse modification.
However, the Act prohibits
unauthorized take of listed species and
requires consultation for activities that
may affect them, including habitat
alterations, regardless of whether
critical habitat has been designated.
When a Federal nexus exists, we work
with the appropriate Federal agency,
and in some cases the applicant to the
consultation, to ensure that the project
can be completed without jeopardizing
the species or adversely modifying
critical habitat. We intend to continue
working with our Federal partners to
provide technical assistance,
coordination, and, in some instances,
section 7 consultation. We do not
anticipate that the listing of these
species or the designation of critical
habitat for the Pecos assiminea will
preclude projects such as riparian
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restoration, fire prevention/
management, or oil and gas
development activities.
Similarly, actions on private lands
that have the potential to result in take
of any of the four invertebrate species
would be subject to section 10 of the
Act, which requires development of a
Habitat Conservation Plan as part of an
application to the Service for an
incidental take permit. These incidental
take permits are issued pursuant to
section 10(a)(1)(B) of the Act. Critical
habitat has possible effects on activities
conducted by non-Federal entities only
if they are conducting activities on
Federal lands or that involves Federal
funding, a Federal permit, or other
Federal action (e.g., grazing permits).
Regulations at 50 CFR 424.02(j) define
special management considerations or
protection to mean any methods or
procedures useful in protecting the
physical and biological features of the
environment for the conservation of
listed species. When we designate
critical habitat, we may not have the
information necessary to identify all
areas that are essential for the
conservation of the species.
Nevertheless, we are required to
designate those areas we consider to be
essential, using the best information
available to us. Accordingly, we do not
designate critical habitat in areas
outside the geographical area occupied
by the species unless the best available
scientific and commercial data
demonstrate that unoccupied areas are
essential for the conservation needs of
the species.
The Service’s Policy on Information
Standards Under the Act, published in
the Federal Register on July 1, 1994 (59
FR 34271), and Section 515 of the
Treasury and General Government
Appropriations Act for Fiscal Year 2001
(Pub. L. 106–554; H.R. 5658) and the
associated Information Quality
Guidelines issued by the Service,
provide criteria, establish procedures,
and provide guidance to ensure that
decisions we make represent the best
scientific and commercial data
available. They require our biologists, to
the extent consistent with the Act and
with the use of the best scientific and
commercial data available, to use
primary and original sources of
information as the basis for
recommendations to designate critical
habitat. When determining which areas
are critical habitat, information may be
obtained from the listing package,
recovery plans, articles in peer-reviewed
journals, conservation plans developed
by States and counties or other entities
that develop HCPs, scientific status
surveys and studies, and biological
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assessments. In the absence of
published data, unpublished materials
and expert opinion or personal
knowledge are used.
Areas that support populations, but
are outside the critical habitat
designation, are still important to the
species. Because of that they will
continue to be subject to conservation
actions implemented under section
7(a)(1) of the Act and to the regulatory
protections afforded by the section
7(a)(2) jeopardy standard, as determined
on the basis of the best available
information at the time of the action.
Federally funded or permitted projects
affecting listed species outside their
designated critical habitat areas may
still result in jeopardy findings in some
cases. Similarly, critical habitat
designations made on the basis of the
best available information at the time of
designation will not control the
direction and substance of future
recovery plans, habitat conservation
plans, or other species conservation
planning efforts if new information
available to these planning efforts calls
for different approaches.
In our critical habitat designation we
use the provisions outlined in section
3(5)(A) of the Act to evaluate those
specific areas defined by the features
essential to the conservation of the
species that may require special
management considerations or
protections. On the basis of our
evaluation, we have determined that
BLNWR does not require special
management considerations or
protections, and have excluded this area
from the designation of critical habitat
for these four invertebrates pursuant to
section 3(5)(A) of the Act as discussed
below (see ‘‘Exclusions Under Section
3(5)(A) of the Act’’ section below).
Because the Roswell springsnail,
Koster’s springsnail, and Noel’s
amphipod are only found within or
adjacent to the BLNWR, we are not
designating critical habitat for these
three species. The critical habitat
discussion below only concerns habitat
for the Pecos assiminea.
Primary Constituent Elements
In accordance with section 3(5)(A)(i)
of the Act and regulations at 50 CFR
424.12, in determining which areas to
propose as critical habitat, we consider
those physical and biological features
(primary constituent elements) that are
essential to the conservation of the
species and that may require special
management considerations or
protection. These features include but
are not limited to: space for individual
and population growth and for normal
behavior; food, water, air, light,
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minerals or other nutritional or
physiological requirements; cover or
shelter; sites for germination or seed
dispersal; and habitats that are protected
from disturbance or are representative of
the historical, geographical, and
ecological distributions of a species.
This critical habitat designation does
not include lands on BLNWR, New
Mexico (see Exclusions Under Section
3(5)(A)’’ and ‘‘Summary of Changes to
Proposed Rule’’ sections). We
determined the primary constituent
elements for the Pecos assiminea (the
only species which occurs off of
BLNWR) from data and studies on its
general habitat and life history
requirements including, but not limited
to: Taylor 1987; and NMDGF 1996,
1998, 1999, 2005b, and 2005c. A
description of the essential environment
as it relates to the specific primary
constituent elements required of the
Pecos assiminea is described below.
Space for Individual and Population
Growth and Normal Behavior
The Pecos assiminea requires
saturated, moist soil at stream or spring
run margins. Spring complexes that
contain flowing water create saturated
soils that provide the specific habitat
needed for population growth,
sheltering, and normal behavior of the
species. This snail typically occurs near
the soil surface or beneath leaf litter or
vegetation in these areas (NMDGF
2005b). Consequently, wetland plant
species are required to provide the leaf
litter, shade, and appropriate
microhabitat. Plant species such as
American three-square (Scirpus
americanus), spike rush (Eleocharis
spp), inland saltgrass (Distichlis spicata)
and rushes (Juncus spp.) provide the
appropriate cover and shelter required
Pecos assiminea (NMDGF 2005b).
Water
The Pecos assiminea is found in wet
mud or beneath mats of vegetation,
usually within a few centimeters
(inches) of flowing water. The moist soil
environment provides foraging and
sheltering habitat, as well as habitat
structure necessary for reproduction and
successful recruitment of offspring.
These areas provide the algae, bacteria,
and decaying organic matter on which
this species depends as a food resource.
The Pecos assiminea is rarely found
immersed in water or in standing water.
Therefore, impoundment of
springbrooks or streams is seen as
detrimental to the survival of the
species. It also does not appear to
persist in areas with fluctuating water
levels or in wetlands that freeze (Lang
2000). However, water is essential to the
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conservation of the Pecos assiminea
because the species cannot withstand
permanent drying (loss of surface flow)
of springs or spring complexes. When
water quality conditions degrade (e.g.,
water temperatures are too high, and
dissolved oxygen concentrations are too
low), Pecos assiminea will likely be
injured or die.
Reproduction and Rearing of Offspring
Little is known about the reproductive
requirements for the Pecos assiminea.
The native wetland plant community
was included in this designation
because the Pecos assiminea is found
within the moist environment directly
adjacent to the aquatic habitat.
Substrates found in these margin areas
provide for temperatures within the
environmental tolerance for this species,
and the habitat for reproduction that the
Pecos assiminea requires.
Food
The Pecos assiminea has a file-like
radula (a ribbon of teeth) situated
behind the mouth that is used to graze
or scrape food from the foraging surface.
Saturated soils and wetland vegetation
adjacent to spring complexes contribute
to the necessary components to support
the algae, detritus, and bacteria on
which this species forages.
The discussion above describes the
physical and biological features
essential to the Pecos assiminea and
presents our rationale as to why the
features identified below were selected.
The primary constituent elements
described below include the essential
features of spring complexes that
develop, maintain, and regenerate the
habitat components required for the
Pecos assiminea to forage, reproduce,
and shelter. The specific biological and
physical features, otherwise referred to
as the primary constituent elements,
essential to the conservation of the
Pecos assiminea are:
(1) Permanent, flowing, unpolluted,
fresh to moderately saline water;
(2) Moist or saturated soil at stream or
spring run margins with native
vegetation growing in or adapted to
aquatic or very wet environment, such
as salt grass or sedges; and
(3) Stable water levels with natural
diurnal and seasonal variation.
Criteria for Defining Critical Habitat
Restoring an endangered or
threatened species to the point where it
is recovered is a primary goal of our
Endangered Species Program. To help
guide the recovery effort, we are
required to prepare and implement
recovery plans for all of the listed
species native to the United States
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unless such plan will not promote the
conservation of the species and the
species is therefore exempt from having
a plan developed for it. Recovery plans
describe actions considered necessary
for conservation of the species, establish
criteria for downlisting or delisting
them, and estimate time and cost for
implementing the recovery measures
needed. A final recovery plan formalizes
the recovery strategy for a species, but
is not a regulatory document (i.e.,
recovery plans are advisory documents
because there are no specific
protections, prohibitions, or
requirements afforded to a species based
solely on a recovery plan). Critical
habitat contributes to the overall
recovery strategy for listed species, but
does not by itself achieve recovery plan
goals.
We do not currently have a recovery
plan for Pecos assiminea. Nevertheless,
we have reviewed the recovery plan
developed by the State of New Mexico
(NMDGF 2005b). In designating critical
habitat for the Pecos assiminea, we also
reviewed information within our files
and recommendations contained in
State wildlife resource reports (Balleau
et al. 1999; NMDGF 2005a, 2005b, 1999,
1998, Boghici 1997; Jones and Balleau
1996; and Cole 1985). We also reviewed
the available literature pertaining to
habitat requirements, historic localities,
and current localities for this species.
We are not aware of any reliable
information that is currently available to
us that was not considered in this
designation process. This final
determination constitutes our best
assessment of areas needed for the
conservation of the species. Much
remains to be learned about this species;
should credible new information
become available which contradicts this
designation, we will reevaluate our
analysis and, if appropriate, propose to
modify this critical habitat designation,
depending on available funding and
staffing. We must make this
determination on the basis of the
information available at this time, and
we may not delay our decision until
more information about the species and
its habitat are available (Southwest
Center for Biological Diversity v.
Babbitt, 215 F.3d 58 (D.C. Cir. 2000)).
The designated critical habitat
constitutes our best assessment of the
specific areas that contain the primary
constituent elements for Pecos
assiminea and that may require special
management or protection. The
designated areas are within the
geographical area occupied by Pecos
assiminea populations and currently
have one or more constituent elements
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(see description of primary constituent
elements, above).
Critical Habitat Designation
We designate two units as critical
habitat for the Pecos assiminea (see the
‘‘Regulation Promulgation’’ section of
this final rule for exact boundary
descriptions). These critical habitat
units include primary constituent
elements that provide for the
physiological, behavioral, and
ecological requirements essential for the
conservation of Pecos assiminea. The
designation includes one complex at
Diamond Y Spring and a segment of the
drainage and East Sandia Spring.
Critical habitat units are designated in
portions of Pecos and Reeves Counties,
Texas. Detailed digital files of each unit
can be obtained by contacting the New
Mexico Ecological Services Field Office
(see ADDRESSES section).
A general description of land
ownership in both areas follows:
1. Diamond Y Springs Complex, Pecos
County, Texas. This area comprises a
major population of Pecos assiminea.
The designation includes the Diamond
Y Spring and approximately 6.8 km (4.2
mi) of its outflow, ending at
approximately 0.8 km (0.5 mi)
downstream of the State Highway 18
bridge crossing. Also included is
approximately 0.8 km (0.5 mi) of Leon
Creek upstream of the confluence with
Diamond Y Draw. All surrounding
riparian vegetation and mesic soil
environments within the spring,
outflow, and portion of Leon Creek are
also designated as these areas are
considered habitat for the Pecos
assiminea. This designation is
approximately 153.8 ha (380 ac) of
aquatic and neighboring mesic habitat.
This complex occurs entirely on private
lands. Private land in the immediate
vicinity of the Diamond Y Springs
Complex is managed as a nature
preserve by TNC.
2. East Sandia Spring, Reeves County,
Texas. This spring contains a
population of Pecos assiminea. The
designation includes the springhead
itself, surrounding seeps, and all
submergent vegetation and moist soil
habitat found at the margins of these
areas. These areas are considered habitat
for the Pecos assiminea. This
designation is approximately 6.7 ha
(16.5 ac) of aquatic and neighboring
upland habitat. The site is private land
managed as a nature preserve by TNC.
Exclusions Under Section 3(5)(A) of the
Act
As we undertake the process of
designating critical habitat for a species,
we first evaluate lands defined by those
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physical and biological features
essential to the conservation of the
species for inclusion in the designation
pursuant to section 3(5)(A) of the Act.
We then evaluate lands defined by those
features to assess whether they may
require special management
considerations or protection. As
discussed in the five factor analysis
above, the Pecos assiminea is imperiled
by a multitude of threats such as oil and
gas operations, introduced species,
groundwater contamination and
depletion, drought, risk of wildfire, and
inadequate regulatory mechanisms.
Below we first provide some general
background information on the BLNWR
and the Comprehensive Conservation
Plan (CCP), followed by an analysis
pursuant to section 3(5)(A) of the Act of
the current management provisions on
BLNWR, and an analysis of why we
believe special management is not
required. Pursuant to section 3(5)(A)(i)
of the Act, we consider the areas that we
are excluding on the BLNWR to be
within the geographical range occupied
by the four invertebrate species. As
noted in the environmental assessment,
one of the areas on the BLNWR, the
impoundment complex, contains an
area that could allow for future
expansion of existing populations.
While this area is not known to be
currently occupied, we consider it to be
within the geographical range occupied
by the four invertebrate species because
it is in close proximity to known
occupied areas (i.e., ranging from
approximately 164 to 656 feet (50 to 200
m)), and it would be an area where
section 7 consultations would occur
because of the potential presence of the
four invertebrate species and known
proximity to occupied areas.
The BLNWR was established on
October 8, 1937, by Executive Order
7724 ‘‘as a refuge and breeding ground
for migratory birds and other wildlife.’’
The Refuge Recreation Act (16 U.S.C.
460–1) identifies the refuge as being
‘‘suitable for incidental fish and
wildlife-oriented recreational
development, the protection of natural
resources, and the conservation of
endangered species or threatened
species.’’ The Wilderness Act of 1964
(Pub. L. 88–577) directs the Service to
‘‘maintain wilderness as a naturally
functioning ecosystem’’ on portions of
the Refuge. While the BLNWR was
originally established to save wetlands
vital to the perpetuation of migratory
birds, the isolated gypsum springs,
seeps, and associated wetlands
protected by the Refuge have been
recognized as providing the last known
habitats in the world for several unique
species. Management emphasis of the
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BLNWR is placed on the protection and
enhancement of habitat for endangered
species and Federal candidate species,
maintenance and improvement of
wintering crane and waterfowl habitat,
and monitoring and maintenance of
natural ecosystem values.
The BLNWR sits at a juncture
between the Roswell Artesian
Groundwater Basin and the Pecos River.
These two systems and their
interactions account for the diversity of
water resources on the Refuge,
including sinkholes, springs, wetlands,
oxbow lakes, and riverine habitats. The
BLNWR has a federally reserved water
right that essentially protects
groundwater levels of the Roswell Basin
in the Refuge vicinity. The Refuge has
undergone adjudication of its federally
reserved water rights by the State of
New Mexico (order signed May 1997).
The BLNWR is currently in negotiations
with the New Mexico Interstate Stream
Commission, a State agency responsible
for administering New Mexico’s water
resources, to quantify these reserved
rights (Service 2005).
The National Wildlife Refuge System
Improvement Act of 1997 establishes a
conservation mission for refuges, gives
policy direction to the Secretary of the
Interior and refuge managers, and
contains other provisions such as the
requirement to integrate scientific
principals into the management of the
Refuges. According to Section 7(e)(1)(E)
of the Refuge Improvement Act, all
lands of the Refuge System are to be
managed in accordance with an
approved CCP that will guide
management decisions and set forth
strategies for achieving refuge purposes.
In general, the purpose of the CCP is to
provide long-range guidance for the
management of National Wildlife
Refuges. The Refuge Improvement Act
requires all refuges to have a CCP and
provides the following legislative
mandates to guide the development of
the CCP: (1) Wildlife has first priority in
the management of refuges; (2) wildlifedependent recreation including hunting,
fishing, wildlife observation, wildlife
photography, environmental education
and environmental interpretation are
the priority public uses of the refuge
system, and shall be allowed when
compatible with the refuge purpose; and
(3) other uses have lower priority in the
refuge system and are only allowed if
not in conflict with any of the priority
uses and determined appropriate and
compatible with the refuge purpose.
The CCP must also be revised if the
Secretary determines that conditions
that affect the refuge or planning unit
have changed significantly. In other
words, a CCP must be followed once it
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is approved, and regularly updated in
response to environmental changes or
new scientific information.
The BLNWR has a Final CCP that was
approved in September 1998. The CCP
serves as a management tool to be used
by the Refuge staff and its partners in
the preservation and restoration of the
ecosystem’s natural resources. The plan
is intended to guide management
decisions over the next 5 to 10 years and
sets forth strategies for achieving Refuge
goals and objectives within that
timeframe. Key goals of the CCP related
to these four invertebrates include the
following: (1) To restore, enhance and
protect the natural diversity on the
BLNWR including threatened and
endangered species by (a) appropriate
management of habitat and wildlife
resources on refuge lands and (b) by
strengthening existing and establishing
new cooperative efforts with public and
private stakeholders and partners, and
(2) To restore and maintain selected
portions of a hydrological system that
more closely mimics the natural
processes along the reach of the Pecos
River adjacent to the BLNWR by: (a)
restoration of the river channel, as well
as restoration of threatened, endangered,
and special concern species; and (b)
control of exotic species and manage
trust responsibilities for maintenance of
plant and animal communities and to
satisfy traditional recreational demands.
Specific objectives related to these goals
include: (1) The restoration of
populations of aquatic species
designated as endangered, threatened,
or of special concern to a sustainable
level (aquatic species in these categories
include the four invertebrates), and (2)
the monitoring of wildlife populations,
including endemic snails.
As explained in detail above, we
believe that BLNWR lands are already
managed for the conservation of wildlife
and special management considerations
or protections are not required.
Therefore, these lands do not meet the
definition of critical habitat, and we are
not designating critical habitat for the
four invertebrate species within
BLNWR.
Critical habitat receives protection
from destruction or adverse
modification through required
consultation under section 7 of the Act.
The section 7 consultation process is
triggered when a Federal agency
determines that its proposed Federal
action (i.e., an action that it funds,
carries out, or authorizes) may affect a
listed species or its critical habitat.
Thus, the principal benefit of any
designated critical habitat is that
Federal activities that may affect critical
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habitat require consultation under
section 7 of the Act.
Once consultation under section 7 of
the Act is triggered, the process may
conclude informally when the Service
concurs in writing that the proposed
Federal action is not likely to adversely
affect the listed species or its critical
habitat. However, if the Service
determines through informal
consultation that adverse impacts are
likely to occur, then formal consultation
is initiated. Formal consultation
concludes with a biological opinion
issued by the Service on whether the
proposed Federal action is likely to
jeopardize the continued existence of a
listed species or result in destruction or
adverse modification of critical habitat,
with separate analyses being made
under both the jeopardy and the adverse
modification standards. For critical
habitat, a biological opinion that
concludes in a determination of no
destruction or adverse modification may
contain discretionary conservation
recommendations to minimize adverse
effects to primary constituent elements,
but it would not contain any mandatory
reasonable and prudent measures or
terms and conditions. Mandatory
reasonable and prudent alternatives to
the proposed Federal action would only
be issued when the biological opinion
results in a jeopardy or adverse
modification conclusion.
The designation of critical habitat
does not imply that lands outside of
critical habitat do not play an important
role in the conservation of these four
invertebrate species. Federal activities
that may affect those unprotected areas
(such as groundwater pumping, oil and
gas activities, and livestock grazing, etc.)
outside of critical habitat are still
subject to review under section 7 of the
Act if they may affect these species. The
prohibitions of section 9 of the Act (e.g.,
harm, harass, capture) also continue to
apply both inside and outside of
designated critical habitat.
Effect of Critical Habitat Designation
Section 7 Consultation
Section 7(a)(2) of the Act requires
Federal agencies, including us, to insure
that their actions are not likely to
jeopardize the continued existence of a
listed species or result in the
destruction or adverse modification of
designated critical habitat. This
requirement is met through section 7
consultation under the Act. Our
regulations define ‘‘jeopardize the
continued existence of’’ as to engage in
an action that reasonably would be
expected, directly or indirectly, to
reduce appreciably the likelihood of
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both the survival and recovery of a
listed species in the wild by reducing
the reproduction, numbers, or
distribution of that species (50 CFR
402.02). ‘‘Destruction or adverse
modification of designated critical
habitat’’ for this species would include
habitat alterations that appreciably
diminish the value of critical habitat by
significantly affecting any of those
physical or biological features that were
the basis for determining the habitat to
be critical. We are currently reviewing
the regulatory definition of adverse
modification in relation to the
conservation of the species.
If we issue a biological opinion
concluding that a project is likely to
result in the destruction or adverse
modification of critical habitat, we also
provide ‘‘reasonable and prudent
alternatives’’ to the project, if any are
identifiable. Reasonable and prudent
alternatives are defined at 50 CFR
402.02 as alternative actions identified
during consultation that can be
implemented in a manner consistent
with the intended purpose of the action,
that are consistent with the scope of the
Federal agency’s legal authority and
jurisdiction, that are economically and
technologically feasible, and that the
Service’s Regional Director believes
would avoid the likelihood of
jeopardizing the continued existence of
listed species or resulting in the
destruction or adverse modification of
critical habitat. Reasonable and prudent
alternatives can vary from slight project
modifications to extensive redesign or
relocation of the project. Costs
associated with implementing a
reasonable and prudent alternative are
similarly variable.
Activities on Federal lands that may
affect the four invertebrates or their
habitat will require consultation
pursuant to section 7 of the Act.
Activities on State or private lands
requiring a permit from a Federal
agency, such as a permit from the U.S.
Army Corps of Engineers, or some other
Federal action, including funding, will
continue to be subject to the section 7
consultation process. Federal actions
not affecting listed species or critical
habitat, and actions on non-Federal
lands that are not federally funded,
authorized, or permitted, do not require
section 7 consultations.
Section 4(b)(8) of the Act requires us
to evaluate briefly and describe, in any
proposed or final regulation that
designates critical habitat, those
activities involving a Federal action that
may adversely modify such habitat or
that may be affected by such
designation. Activities that may destroy
or adversely modify critical habitat
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include those that alter the primary
constituent elements to an extent that
the value of critical habitat for both the
survival and recovery of the Pecos
assiminea is appreciably reduced. We
note that such activities may also
jeopardize the continued existence of
the species. Activities that, when
carried out, funded, or authorized by a
Federal agency that may affect the Pecos
assiminea and may require consultation
under section 7 of the Act to determine
if they adversely modify critical habitat
include, but are not limited to:
(1) Any activity that would
significantly alter the source-water
capture zone, subterranean flows, or
water level of the supporting aquifers
(groundwater pumping), including any
activity that would significantly alter
the water chemistry, water quality, or
physical parameters (e.g., temperature,
pH, contaminants), or wastewater or
point-source discharge permits in the
wetland habitats and systems that could
appreciably diminish the primary
constituent elements where this species
occurs;
(2) Any activity that would introduce,
spread, or augment non-native aquatic
predators or competitors, or non-native
species that negatively alter Pecos
assiminea habitat or primary constituent
elements: this would include the
introduction of non-native species
through contaminated sampling gear,
bait-bucket introductions of non-native
fishes, or the release of aquarium
species (fish, aquatic snails, and aquatic
plants) from uninformed members of the
public; or
(3) Any activity that would
detrimentally alter the habitat for Pecos
assiminea. This would include water
diversion, drainage alteration projects,
road construction, construction of
public and private facilities, or ponding
of spring runs.
Specific examples of Federal activities
include, but are not limited to, EPA
authorization of discharges under the
National Pollutant Discharge
Elimination System and registration of
pesticides; Federal Highway
Administration approval or funding of
road or highway infrastructure and
maintenance; BLM issuance of oil and
gas leases or permits; U.S. Army Corps
of Engineers authorization of discharges
of dredged or fill material into waters of
the United States under section 404 of
the Clean Water Act; USDA-Natural
Resources Conservation Service
technical assistance and other programs;
USDA-Rural Utilities Service
infrastructure or development; Federal
Energy Regulatory Commission
permitting activities; and the
Department of Housing and Urban
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Development’s Small Cities Community
Development Block Grant and home
loan programs.
Available Conservation Measures
Conservation measures provided to
species listed as endangered or
threatened under the Act include
recognition, recovery actions,
requirements for Federal protection, and
prohibitions against certain practices.
Recognition through listing encourages
and results in conservation actions by
Federal, State, and private agencies,
groups, and individuals. The Act
provides for possible land acquisition
and cooperation with the States and
authorizes recovery plans for all listed
species. The protection required of
Federal agencies and the prohibitions
against certain activities involving listed
animals are discussed in the ‘‘Effect of
Critical Habitat Designation’’ section
above.
Section 7(a) of the Act, as amended,
requires Federal agencies to evaluate
their actions with respect to any species
that is proposed to be listed or is listed
as endangered or threatened, and with
respect to its critical habitat, if any is
being designated. Regulations
implementing this interagency
cooperation provision of the Act are
codified at 50 CFR part 402. Federal
agencies are required to confer with us
informally on any action that is likely to
jeopardize the continued existence of a
proposed species, or result in
destruction or adverse modification of
proposed critical habitat. If a species is
listed subsequently, section 7(a)(2)
requires Federal agencies to ensure that
activities they authorize, fund, or carry
out are not likely to jeopardize the
continued existence of such a species or
to destroy or adversely modify its
critical habitat. If a Federal agency
action may affect a listed species or its
critical habitat, the responsible Federal
agency must enter into formal
consultation with us. Federal agency
actions that may affect the four
invertebrates throughout their range and
may require consultation with us
include, but are not limited to, oil and
gas development, irrigated agricultural
and livestock activities, residential and
commercial development, non-native
vegetation control, fire suppression,
controlled burns, water control
structures, and habitat enhancement
projects.
Listing the four invertebrates provides
for the development and
implementation of a rangewide recovery
plan. This plan will bring together
Federal, State, and local agency efforts
for the conservation of these species. A
recovery plan will establish a
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framework for agencies to coordinate
their recovery efforts. The plan will set
recovery priorities and estimate the
costs of the tasks necessary to
accomplish the priorities. It also will
describe the site-specific actions
necessary to achieve conservation and
survival of the species.
Listing also will require us to review
any actions that may affect the four
invertebrates for lands and activities
under Federal jurisdiction, State plans
developed pursuant to section 6 of the
Act, scientific investigations of efforts to
enhance the propagation or survival of
the animal pursuant to section
10(a)(1)(A) of the Act, and habitat
conservation plans prepared for nonFederal lands and activities pursuant to
section 10(a)(1)(B) of the Act.
Federal agencies with management
responsibility for the four invertebrates
include the Service, in relation to the
issuance of section 10(a)(1)(A) and (B)
permits for scientific research, habitat
conservation plans, BLNWR
management and maintenance, and
other programs.
The Act and implementing
regulations found at 50 CFR 17.21 set
forth a series of general prohibitions and
exceptions that apply to all endangered
wildlife. These prohibitions, in part,
make it illegal for any person subject to
the jurisdiction of the United States to
take (includes harass, harm, pursue,
hunt, shoot, wound, kill, trap, or collect,
or to attempt any of these), import or
export, ship in interstate commerce in
the course of commercial activity, or sell
or offer for sale in interstate or foreign
commerce any listed species. It also is
illegal to possess, sell, deliver, carry,
transport, or ship any such wildlife that
has been taken illegally. Certain
exceptions apply to agents of the U.S.
Fish and Wildlife Service and State
conservation agencies.
Permits may be issued to carry out
otherwise prohibited activities
involving endangered wildlife species
under certain circumstances.
Regulations governing permits are at 50
CFR 17.22 and 17.23. Such permits are
available for scientific purposes, to
enhance the propagation or survival of
the species, or for incidental take in the
course of otherwise lawful activities.
Pursuant to the Interagency
Cooperative Policy for Endangered
Species Act Section 9 Prohibitions,
published in the Federal Register on
July 1, 1994 (59 FR 34272), we identify
to the maximum extent practicable
those activities that would or would not
constitute a violation of section 9 of the
Act. The intent of this policy is to
increase public awareness as to the
effects of this listing on future and
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ongoing activities within the species’
range. We believe, based on the best
available information that the following
actions will not result in a violation of
the provisions of section 9 of the Act,
provided these actions are carried out in
accordance with existing regulations
and permit requirements:
(1) Possession, delivery, or movement,
including interstate transport that does
not involve commercial activity, of
specimens of these species that were
legally acquired prior to the publication
in the Federal Register of the Federal
List of Endangered and Threatened
Wildlife and Plants;
(2) Oil and gas exploration and
drilling in areas where surface or
groundwater is not connected to
habitats occupied by the Roswell
springsnail, Koster’s springsnail, Pecos
assiminea, and Noel’s amphipod; and
(3) Any actions that may affect the
Roswell springsnail, Koster’s
springsnail, Noel’s amphipod, and
Pecos assiminea that are authorized,
funded, or carried out by a Federal
agency (e.g., prescribed burns,
pesticide/herbicide application,
pipeline construction crossing suitable
habitat, oil and gas development or
extraction activities), when the action is
conducted in accordance with the
consultation requirements for listed
species pursuant to section 7 of the Act.
Potential activities involving these
species that we believe will likely be
considered a violation of section 9
include, but are not limited to, the
following:
(1) Unauthorized possession,
collecting, trapping, capturing, killing,
harassing, sale, delivery, or movement,
including interstate, and foreign
commerce, or harming, or attempting
any of these actions, of the Roswell
springsnail, Koster’s springsnail, Noel’s
amphipod, and Pecos assiminea.
Research activities where these species
are trapped or captured will require a
permit under section 10(a)(1)(A) of the
Act;
(2) The use of chemical insecticides or
herbicides that results in killing or
injuring these species;
(3) Intentional release of exotic
species (including, but not limited to,
mosquitofish, crayfish, or non-native
snails) into habitat currently occupied
by the Roswell springsnail, Koster’s
springsnail, Noel’s amphipod, and
Pecos assiminea;
(4) Within the 12,585 ac (5,093 ha) of
the Federal mineral estate and 9,945 ac
(4,025 ha) habitat protection zone in
New Mexico (e.g., BLM 2002, Balleau et
al. 1999), subsurface drilling or similar
activities that contaminate or cause
significant degradation of surface
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drainage water or aquifer water quality
that supports the habitat occupied by
these species;
(5) Septic tank placement and use
where the groundwater is connected to
sinkhole or other aquatic habitats
occupied by these species;
(6) Unauthorized discharges or
dumping of toxic chemicals, silt, or
other pollutants into, or other illegal
alteration of the areas supporting
Roswell springsnail, Koster’s
springsnail, Noel’s amphipod, and
Pecos assiminea that results in death or
injury of the species or that results in
degradation of their occupied habitat to
an extent that individuals are killed or
injured or essential behaviors such as
breeding, feeding, and sheltering are
impaired; and
(7) Destruction or alteration of the
Roswell springsnail, Koster’s
springsnail, Noel’s amphipod, and
Pecos assiminea occupied habitat
through discharge of fill materials into
occupied sites; draining, ditching,
tilling, channelization, drilling,
pumping, or other activities that
interrupt surface or ground water flow
into or out of the spring complexes, and
occupied habitats of these species that
results in killing or injuring these
species by significantly impairing
essential life-sustaining requirements
such as breeding, feeding, and shelter.
If you have questions regarding
whether specific activities will likely
violate the provisions of section 9 of the
Act, contact the New Mexico Ecological
Services Field Office (see ADDRESSES
section). For Pecos assiminea in Texas,
contact the Austin Ecological Services
Field Office, 10711 Burnet Road, Suite
200, Austin, Texas 78758 (512/490–
0057). Requests for copies of the
regulations on listed wildlife and
inquiries about prohibitions and permits
may be addressed to the U.S. Fish and
Wildlife Service, Division of
Endangered Species, P.O. Box 1306,
Albuquerque, New Mexico 87103
(telephone 505/248–6920; facsimile
505/248–6788).
Economic Analysis
Section 4(b)(2) of the Act requires us
to designate critical habitat on the basis
of the best scientific and commercial
data available and to consider the
economic impact, impact to national
security, and other relevant impacts of
designating a particular area as critical
habitat. We based this designation on
the best available scientific information.
We utilized the economic analysis, and
took into consideration comments and
information submitted during the public
hearing and comment periods to make
this final listing and critical habitat
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determination. We may exclude areas
from critical habitat upon a
determination that the benefits of such
exclusions outweigh the benefits of
specifying such areas as critical habitat.
We cannot exclude such areas from
critical habitat when such exclusion
will result in the extinction of the
species.
A draft analysis of the economic
effects of the proposed critical habitat
designation was prepared and made
available for public review (70 FR
23083; May 4, 2005). The economic
analysis considers the economic
impacts of conservation measures taken
prior to and subsequent to the final
listing and designation of critical habitat
for the four invertebrates. Predesignation impacts are typically
defined as all management efforts that
have occurred since the time of listing.
The four invertebrates have not been
listed, but were proposed for listing in
February 2002 (67 FR 6459). Total postdesignation costs associated with
proposed critical habitat Units 3 and 4
for the Pecos assiminea on TNC lands in
Texas are estimated to be $707,000 over
the next 20 years (Service 2005a).
Estimated costs include creating a
conservation plan to formally assess
conservation elements and future
management actions within proposed
critical habitat Units 3 and 4.
Additionally, future costs to oil and gas
activities within proposed Unit 3 are
anticipated to be related to continued
partnership projects between TNC and
regional oil and gas companies.
Based upon these estimates, we
conclude in the final analysis, which
reviewed and incorporated public
comments, that no significant economic
impacts (i.e., will not have annual effect
on the economy of $100 million or more
or affect the economy in a material way
discussed further in the ‘‘Required
Determinations’’ section below) are
expected from the designation of critical
habitat for Pecos assiminea. A copy of
the economic analysis is included in our
supporting record and may be obtained
by contacting the New Mexico
Ecological Services Field Office (see
ADDRESSES section) or from our Web site
https://ifw2es.fws.gov/.
Required Determinations
Regulatory Planning and Review
In accordance with Executive Order
12866, this document is a significant
rule because it may raise novel legal and
policy issues. However, based on our
final economic analysis, it is not
anticipated that the designation of
critical habitat for the four invertebrate
species will result in an annual effect on
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the economy of $100 million or more or
affect the economy in a material way.
Due to the timeline for publication in
the Federal Register, the Office of
Management and Budget (OMB) has not
formally reviewed the final rule or
accompanying economic analysis.
Further, Executive Order 12866
directs Federal Agencies promulgating
regulations to evaluate regulatory
alternatives (Office of Management and
Budget, Circular A–4, September 17,
2003). Pursuant to Circular A–4, once it
has been determined that the Federal
regulatory action is appropriate, then
the agency will need to consider
alternative regulatory approaches. Since
the determination of critical habitat is a
statutory requirement pursuant to the
Endangered Species Act of 1973, as
amended (Act) (16 U.S.C. 1531 et seq.),
we must then evaluate alternative
regulatory approaches, where feasible,
when promulgating a designation of
critical habitat.
In developing our designations of
critical habitat, we consider economic
impacts, impacts to national security,
and other relevant impacts pursuant to
section 4(b)(2) of the Act. Based on the
discretion allowable under this
provision, we may exclude any
particular area from the designation of
critical habitat providing that the
benefits of such exclusion outweighs the
benefits of specifying the area as critical
habitat and that such exclusion would
not result in the extinction of the
species. As such, we believe that the
evaluation of the inclusion or exclusion
of particular areas, or combination
thereof, in a designation constitutes our
regulatory alternative analysis.
Regulatory Flexibility Act (5 U.S.C. 601
et seq.)
Under the Regulatory Flexibility Act,
5 U.S.C. 601 et seq., as amended by the
Small Business Regulatory Enforcement
Act, (SBREFA) 5 U.S.C. 802 (2),
whenever an agency is required to
publish a notice of rulemaking for any
proposed or final rule, it must prepare
and make available for public comment
a regulatory flexibility analysis that
describes the effect of the rule on small
entities (i.e., small businesses, small
organizations, and small government
jurisdictions). However, no regulatory
flexibility analysis is required if the
head of an agency certifies the rule will
not have a significant economic impact
on a substantial number of small
entities. Our economic analysis of the
proposed designation provides the
factual basis for our determination.
According to the Small Business
Administration (SBA), small entities
include small organizations, such as
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independent nonprofit organizations
and small governmental jurisdictions,
including school boards and city and
town governments that serve fewer than
50,000 residents, as well as small
businesses (13 CFR 121.201). Small
businesses include manufacturing and
mining concerns with fewer than 500
employees, wholesale trade entities
with fewer than 100 employees, retail
and service businesses with less than $5
million in annual sales, general and
heavy construction businesses with less
than $27.5 million in annual business,
special trade contractors doing less than
$11.5 million in annual business, and
agricultural businesses with annual
sales less than $750,000. To determine
if potential economic impacts to these
small entities are significant, we
considered the types of activities that
might trigger regulatory impacts under
this designation as well as types of
project modifications that may result. In
general, the term significant economic
impact is meant to apply to a typical
small business firm’s business
operations.
Activities anticipated to occur within
the next 20 years within or adjacent to
critical habitat for the Pecos assiminea
that potentially effect small businesses
include: oil and gas production,
irrigated agricultural production, and
livestock operations.
With regard to livestock operations
the economic analysis finds that
confined animal feeding facilities do not
occur in Pecos or Reeves Counties,
Texas, within 60 miles of the critical
habitat designation. As such, the
analysis does not anticipate impacts to
small entities within the livestock
industry in these counties.
Agricultural production dependent on
groundwater irrigation occurs within
Pecos and Reeves Counties, Texas. The
analysis assumes that all farms
operating within the regions are small
entities. Within Texas, further
hydrological studies are necessary to
determine the impact of groundwater
pumping on surface and groundwater
levels to designated critical habitat. As
a result, groundwater withdrawal
activities for agricultural production are
unlikely to change as a result of the
presence of the Pecos assiminea. Thus,
no impacts to small entities within the
irrigated agricultural industry are
expected.
Oil and gas drilling occurs on private
lands outside of critical habitat Unit 3
(Diamond Y Springs Complex) in Texas.
The economic analysis finds that while
oil and gas activities may present water
quality issues, they are not considered
a threat to groundwater levels in the
region. The analysis does not forecast
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modifications to oil and gas production
in Texas and therefore no impacts to
small businesses are quantified. This is
due to the fact that Unit 3 is owned and
managed by TNC. TNC manages this
area as a preserve for long term habitat
conservation and protection of the
functional integrity of surface water
systems to benefit rare aquatic species
and communities within the preserves.
TNC does not own the mineral rights at
Unit 3. However, the companies that
own or lease these rights have generally
worked voluntarily with TNC to protect
these lands. The economic analysis
finds that future costs to oil and gas
activities within Unit 3 are anticipated
to be related to continued partnership
projects between TNC and regional oil
and gas companies. There may also be
a potential for costs associated with an
incidental take permit and Habitat
Conservation Plan under section 10 of
the Act. However, the economic
analysis finds that the potential for that
occurrence is unknown.
There has been one section 7
consultation on an oil and gas project
with Federal involvement in the vicinity
of habitats occupied by the four
invertebrates. This was an informal
consultation in 2004 regarding proposed
abandonment of 58 miles of pipeline in
Winkler, Ward, Reeves, and Pecos
counties, Texas (Service 2004b). The
proposed project involved permitting by
the Federal Energy Regulatory
Commission. It was determined that the
proposed action would not have any
affect on any of the four invertebrate
species or any co-occurring, listed,
aquatic taxa such as Leon Springs
pupfish. There were no conservation
recommendations made by the Service
regarding protection of aquatic habitats
in this consultation. Based upon this
and other information presented in the
draft economic analysis and draft
environmental assessment, we do not
anticipate economic costs to small
businesses in this industry. Therefore,
we have considered whether this rule
would result in a significant economic
effect on a substantial number of small
entities. We have concluded that this
final designation of critical habitat for
the Pecos assiminea would not affect a
substantial number of small entities.
Therefore, we are certifying that the
designation of critical habitat for the
Pecos assiminea will not have a
significant economic impact on a
substantial number of small entities,
and a final regulatory flexibility analysis
is not required.
Executive Order 13211
On May 18, 2001, the President issued
Executive Order (E.O.) 13211 on
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regulations that significantly affect
energy supply, distribution, and use.
E.O. 13211 requires agencies to prepare
Statements of Energy Effects when
undertaking certain actions. This final
rule is considered a significant
regulatory action under E.O. 12866 due
to it potentially raising novel legal and
policy issues, but the economic analysis
finds that the oil and gas industry is not
likely to experience ‘‘a significant
adverse effect’’ as a result of
conservation efforts for the four
invertebrates. Appendix A of the draft
economic analysis provides a detailed
discussion and analysis of this
determination. Specifically, two criteria
were determined to be relevant to this
analysis: (1) Reductions in natural gas
production in excess of 25 million mcf
per year, and (2) increases in the cost of
energy production in excess of one
percent. Impacts to ongoing oil and gas
production in Pecos County, Texas, are
not forecast as it is unclear whether
these activities will require conservation
efforts for the Pecos assiminea. As
described in Section 4.2.1 of the
economic analysis and above, while oil
and gas activities in this region may
affect groundwater quality, they are not
anticipated to affect groundwater levels.
Unfunded Mandates Reform Act (2
U.S.C. 1501 et seq.)
In accordance with the Unfunded
Mandates Reform Act (2 U.S.C. 1501),
the Service makes the following
findings:
(a) This rule will not produce a
Federal mandate. In general, a Federal
mandate is a provision in legislation,
statute or regulation that would impose
an enforceable duty upon State, local, or
Tribal governments, or the private sector
and includes both ‘‘Federal
intergovernmental mandates’’ and
‘‘Federal private sector mandates.’’
These terms are defined in 2 U.S.C.
658(5)–(7). ‘‘Federal intergovernmental
mandate’’ includes a regulation that
‘‘would impose an enforceable duty
upon State, local, or Tribal
governments’’ with two exceptions. It
excludes ‘‘a condition of Federal
assistance.’’ It also excludes ‘‘a duty
arising from participation in a voluntary
Federal program,’’ unless the regulation
‘‘relates to a then-existing Federal
program under which $500,000,000 or
more is provided annually to State,
local, and Tribal governments under
entitlement authority,’’ if the provision
would ‘‘increase the stringency of
conditions of assistance’’ or ‘‘place caps
upon, or otherwise decrease, the Federal
Government’s responsibility to provide
funding’’ and the State, local, or Tribal
governments ‘‘lack authority’’ to adjust
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accordingly. (At the time of enactment,
these entitlement programs were:
Medicaid; AFDC work programs; Child
Nutrition; Food Stamps; Social Services
Block Grants; Vocational Rehabilitation
State Grants; Foster Care, Adoption
Assistance, and Independent Living;
Family Support Welfare Services; and
Child Support Enforcement.) ‘‘Federal
private sector mandate’’ includes a
regulation that ‘‘would impose an
enforceable duty upon the private
sector, except (i) a condition of Federal
assistance; or (ii) a duty arising from
participation in a voluntary Federal
program.’’
The designation of critical habitat
does not impose a legally binding duty
on non-Federal government entities or
private parties. Under the Act, the only
regulatory effect is that Federal agencies
must ensure that their actions do not
destroy or adversely modify critical
habitat under section 7. While nonFederal entities who receive Federal
funding, assistance, permits or
otherwise require approval or
authorization from a Federal agency for
an action may be indirectly impacted by
the designation of critical habitat, the
legally binding duty to avoid
destruction or adverse modification of
critical habitat rests squarely on the
Federal agency. Furthermore, to the
extent that non-Federal entities are
indirectly impacted because they
receive Federal assistance or participate
in a voluntary Federal aid program, the
Unfunded Mandates Reform Act would
not apply; nor would critical habitat
shift the costs of the large entitlement
programs listed above on to State
governments.
(b) We do not believe that this rule
will significantly or uniquely affect
small governments. This determination
is based on information from the
economic analysis conducted for this
designation of critical habitat for the
Pecos assiminea and the fact that critical
habitat is only being designated on TNC
lands. As such, a Small Government
Agency Plan is not required.
Takings
In accordance with Executive Order
12630 (‘‘Government Actions and
Interference with Constitutionally
Protected Private Property Rights’’), we
have analyzed the potential takings
implications of proposing critical
habitat for the Pecos assiminea in a
takings implications assessment. The
takings implications assessment
concludes that the designation of
critical habitat for the Pecos assiminea
does not pose significant takings
implications.
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Federalism
In accordance with Executive Order
13132, this rule does not have
significant Federalism effects. A
Federalism assessment is not required.
In keeping with Department of the
Interior policy, the Service requested
information from, and coordinated
development of this critical habitat
designation with, appropriate State
resource agencies in New Mexico and
Texas. The impact of the designation on
State and local governments and their
activities was fully considered in the
economic analysis. As discussed above,
the designation of critical habitat for the
Pecos assiminea would have little
incremental impact on State and local
governments and their activities. In fact,
the designation of critical habitat may
have some benefit to the State and local
resource agencies in that the areas
essential to the conservation of this
species are more clearly defined, and
the primary constituent elements of the
habitat necessary to the conservation of
this species are specifically identified.
Civil Justice Reform
In accordance with Executive Order
12988, the Office of the Solicitor has
determined that the rule does not
unduly burden the judicial system and
that it meets the requirements of
sections 3(a) and 3(b)(2) of the Order.
We are designating critical habitat in
accordance with the provisions of the
Act, as amended. This rule uses
standard property descriptions and
identifies the primary constituent
elements within the designated areas to
assist the public in understanding the
habitat needs that are essential for the
conservation of the Pecos assiminea.
Paperwork Reduction Act of 1995 (44
U.S.C. 3501 et seq.)
This rule does not contain new or
revised information collection for which
Office of Management and Budget
approval is required under the
Paperwork Reduction Act. An agency
may not conduct or sponsor, and a
person is not required to respond to, a
collection of information unless it
displays a currently valid OMB control
number.
National Environmental Policy Act
It is our position that, outside the
Tenth Circuit, we do not need to
prepare environmental analyses as
defined by the NEPA in connection with
designating critical habitat under 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
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Secretarial Order 3206: American
Indian Tribal Rights, Federal-Tribal
Trust Responsibilities, and the
Endangered Species Act
The purpose of Secretarial Order 3206
(Secretarial Order) is to ‘‘clarif(y) the
responsibilities of the component
agencies, bureaus, and offices of the
Department of the Interior and the
Department of Commerce, when actions
taken under authority of the Act and
associated implementing regulations
affect, or may affect, Indian lands, tribal
trust resources, or the exercise of
American Indian tribal rights.’’ If there
is potential that a tribal activity could
cause either direct or incidental take of
a species proposed for listing under the
Act, then meaningful government-togovernment consultation will occur to
try to harmonize the Federal trust
responsibility to tribes and tribal
sovereignty with our statutory
responsibilities under the Act. The
Secretarial Order also requires us to
consult with tribes if the designation of
an area as critical habitat might impact
tribal trust resources, tribally owned fee
lands, or the exercise of tribal rights.
However, no known tribal activities
could cause either direct or incidental
take of the four species in this final rule,
and no tribal lands or tribal trust
resources are anticipated to be affected
by the designation of critical habitat.
List of Subjects in 50 CFR Part 17
References Cited
[(Douglas County v. Babbitt, 48 F.3d
1495 (9th Cir. Ore. 1995), cert. denied
116 S. Ct. 698 (1996).] However, when
the range of the species includes States
within the Tenth Circuit, such as that of
the four invertebrates, pursuant to the
Tenth Circuit ruling in Catron County
Board of Commissioners v. U.S. Fish
and Wildlife Service, 75 F.3d 1429 (10th
Cir. 1996), we undertake a NEPA
analysis for critical habitat designation.
We completed an environmental
assessment and finding of no significant
impact on the designation of critical
habitat for the Pecos assiminea.
I
I
A complete list of all references cited
in this rulemaking is available upon
request from the New Mexico Ecological
Services Field Office (see ADDRESSES
section).
Author
The primary authors of this rule are
the New Mexico Ecological Services
Field Office staff (see ADDRESSES
section) (telephone 505/346–2525).
Species
Vertebrate
population
where endangered
or threatened
Historic Range
Common name
Scientific name
*
SNAILS
*
*
*
Endangered and threatened species,
Exports, Imports, Reporting and
recordkeeping requirements,
Transportation.
Regulation Promulgation
Accordingly, we amend part 17,
subchapter B of chapter I, title 50 of the
Code of Federal Regulations, as set forth
below:
I
PART 17—[AMENDED]
1. The authority citation for part 17
continues to read as follows:
I
Authority: 16 U.S.C. 1361–1407; 16 U.S.C.
1531–1544; 16 U.S.C. 4201–4245; Pub. L. 99–
625, 100 Stat. 3500; unless otherwise noted.
2. Amend § 17.11(h) as follows:
a. Add Pecos assiminea, Koster’s
springsnail, and Roswell springsnail in
alphabetical order under ‘‘SNAILS;’’ and
I b. Add Noel’s amphipod in
alphabetical order under
‘‘CRUSTACEANS,’’ to the List of
Endangered and Threatened Wildlife to
read as follows:
§ 17.11 Endangered and threatened
wildlife.
*
*
*
(h) * * *
When
listed
Status
*
*
Pecos assiminea ........
*
Assiminea pecos ........
*
*
U.S.A. (NM, TX) .........
NA
*
Springsnail, Koster’s ...
Springsnail, Roswell ...
*
Juturnia kosteria .........
Pyrgulopsis
roswellensis.
*
*
U.S.A. (NM) ................
U.S.A. (NM) ................
NA
NA
*
Gammarus desperatus
*
*
U.S.A. (NM) ................
NA
*
*
Critical
habitat
*
*
Special
rules
*
E
*
17.95(f)
NA
E
E
*
NA
NA
NA
NA
E
*
NA
NA
*
*
*
CRUSTACEANS
*
Amphipod, Noel’s .......
*
*
*
*
*
*
3. Amend § 17.95 (f) by adding critical
1. Within the areas designated below
habitat for Pecos assiminea in the same
as critical habitat, the primary
order as this species occurs in § 17.11(h). constituent elements for Pecos
assiminea include:
§ 17.95 Critical habitat—fish and wildlife.
(i) Permanent, flowing, unpolluted,
*
*
*
*
*
fresh to moderately saline water;
(f) Clams and snails.
(ii) Moist or saturated soil at stream or
*
*
*
*
*
spring run margins with native
vegetation growing in or adapted to
Pecos assiminea (Assiminea pecos)
I
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*
*
*
aquatic or very wet environment, such
as salt grass or sedges; and
(iii) Stable water levels with natural
diurnal and seasonal variation.
2. Critical habitat is depicted for the
Pecos assiminea in Pecos County, Texas,
at the Diamond Y Springs Complex. The
designation includes the Diamond Y
Spring, which is located at UTM 13–
698261 E, 3431372 N, and 6.8 km (4.2
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mi) of its outflow, ending at UTM 13–
701832 E, 3436112 N, about 0.8 km (0.5
mi) downstream of the State Highway
18 bridge crossing. Also included is 0.8
km (0.5 mi) of Leon Creek upstream of
the confluence with Diamond Y Draw.
All surrounding riparian vegetation and
mesic soil environments within the
spring outflow and portion of Leon
Creek are also designated as these areas
are considered habitat for the Pecos
assiminea. Critical habitat is also
depicted for the Pecos assiminea in
Reeves County, Texas, at the East
Sandia Spring complex. East Sandia
Spring is located at UTM 13–621366 E,
342929 N. Critical habitat includes the
springhead itself, surrounding seeps,
and all submergent vegetation and moist
soil habitat found at the margins of
these areas. These areas are considered
habitat for the Pecos assiminea.
(i) Pecos County, Texas, including the
Diamond Y Springs Complex, located at
longitude –102.923461 and latitude
30.999271, and approximately 6.8 km
(4.2 mi) of the spring outflow ending at
about 0.8 km (0.5 mi) downstream of the
State Highway 18 bridge crossing
(approximately longitude –102.885137
and latitude 31.041405). Also included
is approximately 0.8 km (0.5 mi) of Leon
Creek upstream of the confluence with
Diamond Y Draw. All surrounding
riparian vegetation and mesic soil
environments within the spring,
outflow, and portion of Leon Creek are
also proposed for designation as these
areas are considered habitat for the
Pecos assiminea. Legal description
(geographic projection, North American
Datum 83): Longitude (decimal degrees),
Latitude (decimal degrees):
¥102.905319869746634,
31.022089444891570;
¥102.887036917654868,
31.043947412173729;
¥102.884194716234887,
31.042760908977833;
¥102.885135806784476,
31.040116604685526;
¥102.886447071974004,
31.038190792077721;
¥102.886620885824385,
31.037813677269160;
¥102.890251036381329,
31.035783323856453;
¥102.892481680821120,
31.034679908957198;
¥102.893548121939546,
31.033842414359302;
¥102.893785401930572,
31.033086360646934;
¥102.893745950415067,
31.032373282069056;
¥102.894097678233564,
31.031429114358268;
¥102.895544792411911,
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31.030835296062797;
¥102.896058768051944,
31.030036256911551;
¥102.898010410716566,
31.029070675153459;
¥102.898781252646117,
31.029130733495535;
¥102.899944293890798,
31.028912200684612;
¥102.900716178554276,
31.028924768711160;
¥102.901441262661692,
31.028556604651808;
¥102.901948928625941,
31.028042412007075;
¥102.901688880906221,
31.027325744767865;
¥102.901714918210303,
31.026138774702297;
¥102.901732622700223,
31.025331634924694;
¥102.901817954640350,
31.023955646131167;
¥102.902125889274174,
31.022488286611136;
¥102.902640803335373,
31.021641737279424;
¥102.903610272253857,
31.020185129479138;
¥102.903508335417825,
31.019803505987209;
¥102.904231258688768,
31.019530280313123;
¥102.905008267695379,
31.019305424852949;
¥102.905627160458280,
31.018745526192433;
¥102.905862223627835,
31.018084401107885;
¥102.907438011441329,
31.016637604571564;
¥102.908402165790250,
31.015418349965021;
¥102.909312205831228,
31.014150714293240;
¥102.909665778900688,
31.013111534294385;
¥102.910342839052220,
31.012410065631975;
¥102.911174902560035,
31.012186062876218;
¥102.912113070098556,
31.012153756020012;
¥102.912844195573911,
31.011500644598044;
¥102.913370338091369,
31.010131773029197;
¥102.914161736135028,
31.009242148253836;
¥102.915610463748450,
31.008553125409257;
¥102.917106029547554,
31.008244810453860;
¥102.918875138268959,
31.008035883431738;
¥102.919664405186026,
31.007241180720893;
¥102.920460878479304,
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31.006114116159939;
¥102.920933820519480,
31.004649359449264;
¥102.921603523207537,
31.004280181687651;
¥102.921961044126064,
31.003051041389284;
¥102.922105288280434,
31.001485991578242;
¥102.923062919493049,
31.000551488397821;
¥102.924338893382782,
31.000192054013731;
¥102.925434072210962,
31.000542142822137;
¥102.925748330937964,
31.001307135185360;
¥102.925543882342382,
31.003108703491051;
¥102.924514657475115,
31.004802011677008;
¥102.923332386691257,
31.005922892971402;
¥102.922655466250575,
31.006624436236699;
¥102.921313967399342,
31.007457756682811;
¥102.921298502243019,
31.008169949149053;
¥102.921890429628803,
31.008844431891216;
¥102.922088249987723,
31.009892533060658;
¥102.920305700167233,
31.010718735844538;
¥102.918990962464960,
31.010317563552466;
¥102.917661775715189,
31.010581089582509;
¥102.915939472406691,
31.011170723093645;
¥102.915640066348502,
31.012258293740160;
¥102.915233503111892,
31.013201643466406;
¥102.914004171668253,
31.013941704157816;
¥102.912955733451284,
31.013972240169043;
¥102.912389969275623,
31.014628028040637;
¥102.912099833183859,
31.015288275173923;
¥102.912212159226485,
31.015195101507882;
¥102.910513768505638,
31.017209923999967;
¥102.908484529126227,
31.019219357013320;
¥102.906961764318297,
31.020762017382609;
¥102.906510334381181,
31.021229648922475;
¥102.906323124324715,
31.022224022537589;
¥102.905476410341578,
31.023112694758801;
¥102.904572468616138,
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31.036422464608236;
¥102.892135869908444,
31.037856459486278;
¥102.890355694384951,
31.038539777638526;
¥102.889015567482971,
31.039277771567470;
¥102.888427464446750,
31.040930483816535;
¥102.887036917654868,
31.043947412173729.
(ii) Reeves County, Texas, at the East
Sandia Spring complex. East Sandia
Spring is located at longitude
–103.728918, latitude 30.991012. The
designation includes the springhead
itself, surrounding seeps, and all
submergent vegetation and moist soil
habitat found at the margins of these
areas. These areas are considered habitat
31.024095422710321;
¥102.904098125726293,
31.025607579972412;
¥102.904512146691772,
31.026849198511329;
¥102.904475741511831,
31.028510959127807;
¥102.903447935740203,
31.030109108839046;
¥102.901831302956197,
31.030890242225727;
¥102.900225068829968,
31.031196566903024;
¥102.897834397853146,
31.032060033587637;
¥102.896823149655987,
31.032898465556570;
¥102.895449713462554,
31.035155846795476;
¥102.894484140543042,
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46331
for the Pecos assiminea. Legal
description (geographic projection,
North American Datum 83): Longitude
(decimal degrees), Latitude (decimal
degrees): –103.729296238487009,
30.990656960487129;
–103.731179077171333,
30.989695620405591;
–103.730160658036496,
30.991850361242875;
–103.727182653076312,
30.992477028891606;
–103.729159475230986,
30.988608062418542;
–103.731179077171333,
30.989695620405591.
3. A map of the Diamond Y Springs
Complex and East Sandia Spring
Complex follows:
BILLING CODE 4310–55–P
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Federal Register / Vol. 70, No. 152 / Tuesday, August 9, 2005 / Rules and Regulations
Dated: August 1, 2005.
Craig Manson,
Assistant Secretary for Fish and Wildlife and
Parks.
[FR Doc. 05–15486 Filed 8–8–05; 8:45 am]
BILLING CODE 4310–55–C
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Agencies
[Federal Register Volume 70, Number 152 (Tuesday, August 9, 2005)]
[Rules and Regulations]
[Pages 46304-46333]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 05-15486]
[[Page 46303]]
-----------------------------------------------------------------------
Part III
Department of the Interior
-----------------------------------------------------------------------
Fish and Wildlife Service
-----------------------------------------------------------------------
50 CFR Part 17
Endangered and Threatened Wildlife and Plants; Listing Roswell
springsnail, Koster's springsnail, Noel's amphipod, and Pecos assiminea
as Endangered With Critical Habitat; Final Rule
Federal Register / Vol. 70, No. 152 / Tuesday, August 9, 2005 / Rules
and Regulations
[[Page 46304]]
-----------------------------------------------------------------------
DEPARTMENT OF THE INTERIOR
Fish and Wildlife Service
50 CFR Part 17
RIN 1018-AI15
Endangered and Threatened Wildlife and Plants; Listing Roswell
springsnail, Koster's springsnail, Noel's amphipod, and Pecos assiminea
as Endangered With Critical Habitat
AGENCY: Fish and Wildlife Service, Interior.
ACTION: Final rule.
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SUMMARY: We, the U.S. Fish and Wildlife Service (Service), list the
Roswell springsnail (Pyrgulopsis roswellensis), Koster's springsnail
(Juturnia kosteri), and Noel's amphipod (Gammarus desperatus) as
endangered and the Pecos assiminea (Assiminea pecos) as endangered with
critical habitat under the Endangered Species Act of 1973, as amended
(Act). These four invertebrates occur at sinkholes, springs, and
associated spring runs and wetland habitats. They are found at one site
in Chaves County, New Mexico, and Pecos assiminea is also found at one
site in Pecos County, Texas, and one site in Reeves County, Texas.
These three snails and one amphipod have an exceedingly limited
distribution, low mobility, and fragmented habitat. They are imperiled
by introduced species, surface and groundwater contamination, oil and
gas extraction activities within the supporting aquifer and watershed,
local and regional groundwater depletion, severe drought, and direct
loss of their habitat (e.g., through burning or removing marsh
vegetation, or flooding of habitat). This final rule will implement the
Federal protection and recovery provisions of the Act for these
invertebrate species. We are also designating critical habitat for the
Pecos assiminea in Texas.
DATES: This final rule is effective September 8, 2005.
ADDRESSES: Supporting documentation for this rulemaking is available
for public inspection, by appointment, during normal business hours at
the U.S. Fish and Wildlife Service, New Mexico Ecological Services
Field Office, 2105 Osuna Road NE., Albuquerque, New Mexico 87113.
FOR FURTHER INFORMATION CONTACT: Susan MacMullin, Field Supervisor, New
Mexico Ecological Services Field Office (telephone, 505-761-4706;
facsimile, 505-346-2542).
SUPPLEMENTARY INFORMATION:
Background
It is our intent to discuss only those topics directly relevant to
this final listing determination. For more information on the four
invertebrates, refer to the February 12, 2002, proposed rule (67 FR
6459). However, some of this information is discussed in our analyses
below, such as the summary of factors affecting the species.
Springsnails
The Permian Basin of the southwestern United States contains one of
the largest carbonate (limestone) deposits in the world (New Mexico
Department of Game and Fish (NMDGF) 1998). Within the Permian Basin of
the Southwestern United States lies the Roswell Basin. Located in
southeastern New Mexico, this Basin has a surface area of around 31,080
square kilometers (km) (12,000 square miles [mi]) and generally begins
north of Roswell, New Mexico, and runs to the southeast of Carlsbad,
New Mexico. The Roswell Basin contains a deep artesian aquifer and a
shallow surficial aquifer. The action of water on soluble rocks (e.g.,
limestone and dolomite) has formed abundant ``karst'' features such as
sinkholes, caverns, springs, and underground streams (White et al.
1995). These hydrogeological formations create unique settings
harboring diverse assemblages of flora and fauna. The isolated
limestone and gypsum springs, seeps, and wetlands located in and around
Roswell, New Mexico, and Pecos and Reeves Counties, Texas, provide the
last known habitats in the world for several endemic species of fish,
plants, mollusks, and crustaceans. These species include the Roswell
springsnail and Koster's springsnail of the freshwater snail family
Hydrobiidae, Pecos assiminea of the snail family Assimineidae, and
Noel's amphipod (Gammaridae). These species are distributed in
isolated, geographically separate populations, and likely evolved from
parent species that once enjoyed a wide distribution during wetter,
cooler climates of the Pleistocene. Such divergence has been well-
documented for aquatic and terrestrial macroinvertebrate groups within
arid ecosystems of western North America (e.g., Taylor 1987; Metcalf
and Smartt 1997; Bowman 1981; Cole 1985).
North American snails of the family Hydrobiidae inhabit a great
diversity of aquatic systems from surface to cave habitats, small
springs to large rivers, and high energy riffles to slack water pools
(Wu et al. 1997). Snails of the family Assimineidae are typically found
in coastal brackish waters or along tropical and temperate seacoasts
worldwide (Taylor 1987). Inland species of the genus Assiminea are
known from around the world, and in North America they occur in
California (Death Valley National Monument), Utah, New Mexico, Texas
(Pecos and Reeves Counties), and Mexico (Bols[oacute]n de Cuatro
C[iacute]enegas).
The Roswell springsnail and Koster's springsnail are aquatic
species. These snails have lifespans of 9 to 15 months and reproduce
several times during the spring through fall breeding season (Taylor
1987; Pennak 1989; Brown 1991). Snails of the family Hydrobiidae are
sexually dimorphic (there are characteristic differences between males
and females), with females being characteristically larger and longer-
lived than males. As with other snails in the family, the Roswell
springsnail and Koster's springsnail are completely aquatic but can
survive in seepage areas, as long as flows are perennial and within the
species' physiological tolerance limit. These two snails occupy spring
heads and runs with variable water temperatures (10 to 20 [deg] Celsius
[C] (50 to 68 [deg] Fahrenheit [F])) and slow-to-moderate water
velocities over compact substrate ranging from deep organic silts to
gypsum sands and gravel and compact substrate (NMDGF 1998). Conversely,
the Pecos assiminea seldom occurs immersed in water, but prefers a
humid microhabitat created by wet mud or beneath vegetation mats,
typically within a few centimeters (cm) (inches (in)) of running water.
Gastropods (snails) are a class of mollusks with a body divided
into a foot and visceral mass and a head that usually bears eyes and
tentacles. Like most gastropods, the Roswell springsnail, Koster's
springsnail, and Pecos assiminea feed on algae, bacteria, and decaying
organic material (NMDGF 1988). They will also incidentally ingest small
invertebrates while grazing on algae and detritus (dead or partially
decayed plant materials or animals).
These snails are fairly small; Koster's springsnail is the largest
of the three snails, and is about 4 to 4.5 millimeters (mm) (0.16 to
0.18 in) long with a pale tan shell that is narrowly conical with up to
4\1/4\ to 5\3/4\ whorls or twists. The Roswell springsnail is 3 to 3.5
mm (0.12 to 0.14 in) long with a narrowly conical tan shell with up to
5 whorls. Pecos assiminea is the smallest of the three, with a shell
length of 1.55 to 1.87 mm (0.06 to 0.07 in) and a thin, nearly
transparent chestnut-brown shell that is regularly conical with up to
4\1/2\ strongly incised (shouldered) whorls and a broad oval opening.
Although their shells are
[[Page 46305]]
similar, the Roswell springsnail is distinguished from Koster's
springsnail by a dark, amber operculum (a lid which closes the shell
opening when the animal is retracted) with white spiral streaks, while
that of Koster's springsnail is nearly colorless. The genus Assiminea
can be determined from other snail genera by an almost complete lack of
tentacles, leaving the eyes within the tips of short eye stalks (Taylor
1987).
Taylor (1987) first described the Roswell springsnail from a
``seepage'' along the west side of an impoundment in Area 7 at Bitter
Lake National Wildlife Refuge (BLNWR, Refuge), Chaves County, New
Mexico. Since then, Mehlhop (1992, 1993) has documented the species on
the BLNWR and in March 1995 also found it in a spring on private land
(i.e., North Spring) east of Roswell (NMDGF 1998). In 2004, the Roswell
springsnail was determined to have been extirpated from this private
land through habitat alteration (NMDGF 2005b). Monitoring efforts at
BLNWR (1995 to 1998) led to the discovery of Roswell springsnail
populations in Bitter Creek, the Sago Springs Complex, and a drainage
canal along the west shoreline of Area 6. The Roswell springsnail is
currently known only from BLNWR with the core population in the Sago
Springs Complex and Bitter Creek. The Sago Springs complex is
approximately 0.3 km long (1,000 linear feet), half of which is
subterranean with flow in the upper reaches restricted to sinkholes.
Bitter Creek is six times longer than the Sago Springs Complex and has
a total length of 1.8 km (1.1 miles). Monthly monitoring and ecological
studies of the Roswell springsnail initiated at BLNWR in June 1995 are
ongoing (NMDGF 2005b, 2005c).
Roswell springsnail formerly occurred in several other springs in
the Roswell area, but these habitats have dried up apparently due to
groundwater pumping and no longer contain the species (Cole 1981;
Taylor 1983, 1987). As noted, the Roswell springsnail historically
occurred on private land at North Spring, but could not be found during
surveys in 2004 (NMDGF 2005b). Pleistocene fossils of the Roswell
springsnail are known from Berrendo Creek and the Pecos River in Chaves
County (Taylor 1987). No populations are currently known from these
areas.
Taylor (1987) first reported Koster's springsnail from Sago Spring
at BLNWR. Another population was documented in 1995 at North Spring on
private land east of Roswell and a second population was found at BLNWR
on the west side of Area 3 during extensive surveys conducted between
1998 and 2001 (Warrick 2005). The species formerly occurred in several
other springs in the Roswell area, but these habitats have since dried
up due to groundwater pumping and no longer contain the species (Cole
1981; Taylor 1983, 1987; NMDGF 2005b). Pleistocene fossils of Koster's
springsnail are known from North Spring River and South Spring Creek in
Chaves County (Taylor 1987). Monthly monitoring and ecological studies
of Koster's springsnail initiated at BLNWR in 1995 indicate the species
is most abundant in the deep organic substrates of Bitter Creek (NMDGF
1998, 2005b). It also occurs at the Sago Springs Complex, but in lower
numbers. The species has not been found in recent times along the
western boundary of Area 3 in BLNWR (NMDGF 2005b). Koster's springsnail
has recently been extirpated at North Spring east of Roswell (NMDGF
2005b).
Pecos assiminea is presently known from two sites at BLNWR, Chaves
County, New Mexico, from a large population at Diamond Y Spring and its
associated drainage (Diamond Y Springs Complex), Pecos County, Texas,
and at East Sandia Spring, Reeves County, Texas. It was thought that
Pecos assiminea occurred sporadically throughout the Bolson de Cuatro
Cinegas, Coahuila, Mexico (Taylor 1987); however, recent investigations
indicate that the population in Mexico might be a different species
(Hershler 2005). Investigations are currently underway to determine
whether the animals found in the vicinity of Coahuila, Mexico, are
Pecos assiminea (Hershler 2005).
Monitoring and ecological studies of Pecos assiminea initiated at
BLNWR in 1995 showed the snail to be typically absent from substrate
samples. Populations of Pecos assiminea occur sporadically along Bitter
Creek, and a dense population was confirmed on moist vegetation and on
muddy surfaces within 1 cm (0.39 in) of water in 1999 in an emergent
marsh plant community around the perimeter of a sinkhole within the
Sago Springs Complex (NMDGF 1999).
Noel's amphipod
Noel's amphipod, in the family Gammaridae, is a small freshwater
crustacean. Inland amphipods are sometimes referred to as freshwater
shrimp. Noel's amphipod is brown-green in color with elongate, kidney-
shaped eyes, and flanked with red bands along the thoracic and
abdominal segments, often with a red dorsal stripe. Males are slightly
larger than females, and individuals range from 8.5 to 14.8 mm (0.33 to
0.58 in) long (Cole 1981, 1985).
Gammarids commonly inhabit shallow, cool, well-oxygenated waters of
streams, ponds, ditches, sloughs, and springs (Holsinger 1976; Pennak
1989). Because they are light-sensitive, these bottom-dwelling
amphipods are active mostly at night and feed on algae, submergent
vegetation, and decaying organic matter (Holsinger 1976; Pennak 1989).
Young amphipods depend on microbial foods, such as algae and bacteria,
associated with aquatic plants (Covich and Thorp 1991). Most amphipods
complete their life cycle in one year and breed from February to
October, depending on water temperature (Pennak 1978). Amphipods form
breeding pairs that remain attached for 1 to 7 days at or near the
substrate while continuing to feed and swim (Bousfield 1989). They can
produce from 15 to 50 offspring, forming a ``brood.'' Most amphipods
produce one brood but some species produce a series of broods during
the breeding season (Pennak 1978).
Noel's amphipod is one of three species of endemic amphipods of the
Pecos River Basin occurring from Roswell, New Mexico, south to Fort
Stockton, Texas, known collectively as the Gammarus-pecos complex (Cole
1985). Noel's amphipod is currently known from the following sites at
BLNWR: Sago Springs Complex, Bitter Creek, along the western boundary
of Area 6, Area 7 spring-ditch, and Hunter Marsh. It is also found in a
spring just outside the BLNWR boundary on private property owned by the
City of Roswell (G. Warrick 2005). Noel's amphipod was first described
by Cole (1981) from a 1967 collection of amphipods taken from North
Spring, east of Roswell. Based on morphological similarities, specimens
collected from Lander Springbrook near Roswell were also identified as
Noel's amphipod (Cole 1981). The amphipod was extirpated from Lander
Springbrook between 1951 and 1960, and the North Spring population was
lost between 1978 and 1988. The extirpations were attributed to
regional groundwater depletions and habitat alterations (spring
channelization) respectively (Cole 1981, 1985).
Previous Federal Actions
On November 22, 1985, we received a petition from Mr. Harold F.
Olson, Director of the NMDGF, to add 11 species of New Mexican mollusks
to the Federal list of endangered and threatened wildlife. Roswell
springsnail (Pyrgulopsis roswellensis, formerly Fontelicella
roswellensis (Hershler
[[Page 46306]]
1994)), Koster's springsnail (Juturnia kosteri, formerly Durangonella
kosteri and Tryonia kosteri (Hershler et al. 2002)), and Pecos
assiminea were among the 11 species. We determined that the petition
presented substantial information that the requested action may be
warranted and published a positive 90-day petition finding in the
Federal Register on August 20, 1986 (51 FR 29671). A subsequent 12-
month finding published in the Federal Register on July 1, 1987 (52 FR
24485), concluded that the petitioned action was warranted but
precluded by other higher priority listing actions.
On August 29, 2001, the Service announced a settlement agreement in
response to litigation by the Center for Biological Diversity, the
Southern Appalachian Biodiversity Project, and the California Native
Plant Society. Terms of the agreement required that we submit to the
Federal Register, on or by February 6, 2002, a 12-month finding and
accompanying proposed listing rule and proposed critical habitat
designation for the four invertebrates addressed in this final rule.
This agreement was entered by the court on October 2, 2001 (Center for
Biological Diversity, et al. v. Norton, Civ. No. 01-2063 (JR)
(D.D.C.)). A proposed rule to list the four invertebrates as endangered
with critical habitat was published in the Federal Register on February
12, 2002 (67 FR 6459). On May 31, 2002, we reopened the public comment
period for 90 days (67 FR 6459). In addition, we published newspaper
notices inviting public comment and announcing the public hearing in
the following newspapers in New Mexico: the Carlsbad Current-Argus, the
Artesia Daily Press, the Roswell Daily Record, and the Albuquerque
Journal. On June 18, 2002, we held a public hearing in Carlsbad, New
Mexico, to solicit comments on the proposed rule.
On May 4, 2005, we announced the availability of the draft economic
analysis and draft environmental assessment for the proposal to
designate critical habitat for the four invertebrates (70 FR 23083).
Section 4(b)(2) of the Act requires that we consider economic impacts,
impacts to national security, and other relevant impacts prior to
making a final decision on what areas to designate as critical habitat.
We solicited data and comments from the public on these draft
documents, as well as on all aspects of our proposal, so that we could
consider these in this final determination.
Summary of Comments and Recommendations
In the notices announcing the public comment periods, we requested
that all interested parties submit comments on the proposed listings
and critical habitat designation, as well as on the associated draft
economic analysis and draft environmental assessment, and we also
requested information pertaining to any actions that affect the four
invertebrates; their current status, ecology, distribution, and
threats; and management or conservation efforts in place. We requested
this information in order to make a final listing determination based
on the best scientific and commercial data currently available. We also
solicited four independent experts who are familiar with these species
to peer review the proposed listing and critical habitat designation.
Two of the peer reviewers submitted substantial comments, but did not
support or oppose the proposal. During the public comment periods, we
also received 967 written comments (952 written comments were
identical, in the form of automatically generated emails), and 7
speakers gave verbal comments at the public hearing. Of those oral
comments, one supported the proposal, two were opposed to the proposal,
and four provided additional information. Of the written comments, 956
supported the proposal, 8 were opposed, and 3 were neutral but provided
information. All substantive information provided during the public
comment periods, written and verbal, either has been incorporated
directly into this final determination or is addressed below. Similar
comments are grouped together by issue.
Issue 1: Biological Concerns
(1) Comment: It is unlikely that Melanoides tuberculata, a fully
aquatic animal, competes with Pecos assiminea, a semi-terrestrial
species. On the other hand, the presence of introduced Melanoides
tuberculata could pose a serious threat to aquatic species such as
Koster's springsnail, Roswell springsnail, or Noel's amphipod.
Our Response: The commenter is correct. It is unlikely that
Melanoides would be a competitor with Pecos assiminea and it is very
likely that it may be a serious threat to Koster's springsnail, Roswell
springsnail, and Noel's amphipod. We have a more complete discussion of
the threat of introduced species under the section, ``Summary of
Factors Affecting the Species'' below.
(2) Comment: The NMDGF concluded in 1999 that all four invertebrate
species are stable on the BLNWR. There is no evidence that these
species are at risk.
Our Response: All four invertebrates are classified as Endangered
by the NMDGF under the Wildlife Conservation Act of 1974 (i.e., State
Endangered Species Act) (19 NMAC 33.6.8). As such, the NMDGF supports
the listing and critical habitat designation for these species. They
report that recent (1992 to present) population and habitat monitoring
on BLNWR has documented the persistence of these species; however, they
still face significant threats (Lang 2002, NMDGF 2005a). Our current
understanding of the threats to the four invertebrates and their
habitat are fully described under the ``Summary of Factors Affecting
the Species'' section below.
(3) Comment: Oil and gas development activities in the vicinity of
BLNWR pose no threat to the four invertebrates because the New Mexico
Oil Conservation Division regulations for installation of oil and gas
wells provide protections to limit impacts.
Our Response: The New Mexico Interstate Stream Commission (NMISC)
and NMDGF submitted information that is consistent with the proposed
rule, which indicated oil and gas, residential, or industrial
development on the private lands immediately west of BLNWR may
constitute a threat to spring water quality (Balleau et al. 1999;
McCord et al. 2005; NMDGF 2005a) (see ``Summary of Factors Affecting
the Species'' section below). The NMDGF also presented an overview of
oil and gas production and potential risk to the four invertebrates
(NMDGF 2005a). They note that, although there are no known cases of
groundwater contamination by leaking oil or gas wells in the source-
water capture zone for the Middle Area of BLNWR (discussed further
under ``Water Quality'' section below), groundwater contamination from
petroleum products has been documented north of Roswell (NMDGF 2005a).
There is a history of oil and gas industry operations on and
adjacent to BLNWR, which have resulted in the spillage of oil and brine
onto the BLNWR. For example, annual reports from 1994 to 1998 document
four oil and gas related accidents on and immediately adjacent to BLNWR
(NMDGF 2002; NMISC 2002). In May 1993, a private corporation began
drilling a well on adjacent Bureau of Land Management (BLM) lands when
they hit a water flow with a high chloride content (6,000 parts per
million). The salt water was eventually contained, but serves as an
example of
[[Page 46307]]
potential issues from oil and gas development (Service 2002).
Additionally, in 1996, about 70 to 80 barrels of oil spilled within a
berm on an adjacent oil well located on BLM lands (Service 2002). In
1997, an additional 11 barrels of crude oil leaked into the BLNWR
boundary (Service 2002). In 1998, BLNWR personnel documented probable
violations of New Mexico Oil Conservation Division regulations (e.g., a
substandard pit for drilling cuttings, fire hazards, lack of spillage
notification) (Service 2002; NMISC 2002). In 2000, there was an
additional oil spill on adjacent BLM lands (NMISC 2002).
Development of another 91 natural gas and oil wells has been
anticipated on lands managed by the BLM within the source-water capture
zone (NMDGF 2005a). Contamination of groundwater from underground leaks
has the potential to occur in the future, but existing drilling and
casing regulations by the State of New Mexico's Oil Conservation
Division and requirements of the BLM for oil and gas drilling and
operation in cave and karst areas (BLM 1997) are likely to
substantially reduce this probability. The NMDGF indicates that a more
likely pathway for petroleum-product contamination of groundwater is
from leaking storage and transport facilities from the well site
downstream to processing facilities (NMDGF 2005a). These may include
leaking pipelines, overflowing storage tanks, leaking valves, and other
sources. These data indicate that oil and gas production and
distribution continue to threaten the four invertebrates.
(4) Comment: Contamination threats to the four invertebrates are
not limited to oil and gas development, but also include fire effects.
Immediate and short-term adverse effects have been demonstrated from
the March 2000 Sandhill Fire (NMISC 2002).
Our Response: NMDGF recently reviewed the effects of fire on the
invertebrates (NMDGF 2005a). We agree with their assessment and
summarize much of the information below. We recognize that populations
of these four invertebrates have the potential to be eliminated or
habitat may be rendered unsuitable if fire results in complete
combustion of vegetation and litter, high soil temperatures,
significant amounts of ash flow, large changes in water chemistry
(e.g., dissolved oxygen), or extensive vegetation removal resulting in
soil and litter drying. As such, we have also revised the ``Summary of
Factors Affecting the Species'' section below to include a more
detailed analysis on the threat of wildfire.
(5) Comment: Much of the literature is overly general in nature and
is not site-or species-specific. Including such citations leaves
readers to conclude that a particular author made a statement or
presented data that specifically applies to the threats you believe
exist for these invertebrates.
Our Response: In determining and evaluating threats to the four
invertebrates, we used the best scientific and commercial data
available. This included articles published in peer-reviewed journals,
data collected by NMDGF, and comments received on the proposed rule,
draft economic analysis, and environmental assessment. You are correct
that some of our citations are not specific to these species or the
geographic area. Nevertheless, the citations offer evidence that
certain threats are real for the species because similar examples have
been documented elsewhere.
(6) Comment: The allegation that fire caused significant decreases
in invertebrate populations implies that quantitative sampling was
conducted. The Service and NMDGF rarely conduct quantitative sampling,
and the case may be overstated in your proposal.
Our Response: Extensive quantitative pre- and post-fire monitoring
was conducted by the NMDGF (NMDGF 2005c). Immediately following the
Sandhill fire, Lang (2001) documented a decrease in species richness of
localized populations of aquatic macroinvertebrates. For example, in
1996 densities of Noel's amphipod at Dragonfly Spring were estimated at
11,625 per square meter (m\2\). Out of 74 post-fire monitoring
collections conducted from March 2000 to August 2004, only four Noel's
amphipod were found (NMDGF 2005c).
(7) Comment: Does non-native vegetation such as saltcedar (Tamarix
sp.) threaten the invertebrates? Will New Mexico's ability to eradicate
or manage saltcedar be restricted if these species are listed?
Our Response: Saltcedar management or eradication activities would
be subject to section 7 consultation requirements if a proposed project
has the potential to affect the four invertebrate species or designated
critical habitat. However, the environmental assessment found that some
activities may be considered to be of benefit to the four invertebrate
species (Service 2005). Examples of such beneficial actions could
include removal and control of non-native vegetation, restoration of
wetlands, and removal of non-native species.
Non-native saltcedar is present on BLNWR and The Nature Conservancy
(TNC) lands at the Diamond Y Spring and East Sandia Springs preserves
(Service 2005). This non-native species is currently being controlled
where possible by BLNWR and TNC staff. Control and removal of non-
native vegetation was identified as a factor responsible for
extirpation of localized populations of Pecos assiminea in Mexico and
New Mexico (Taylor 1987). However, it is possible that removal and
control of saltcedar will improve habitat and hydrologic conditions at
springs and seeps (Service 2005). See also ``Factor C'' under the
``Summary of Factors Affecting the Species'' section below.
(8) Comment: Have laboratory toxicity tests been conducted to
determine the four invertebrates' sensitivity to low oxygen, sediments,
or contaminants?
Our Response: To our knowledge, laboratory tests have not been
conducted specifically on these species to determine their sensitivity
to low oxygen, sediments, or contaminants.
(9) Comment: Equating the springsnails with Higgin's eye mussel is
inappropriate. Clearly, clams and mussels are very different creatures
than springsnails.
Our Response: The commenter is correct that mussels that live in
the substrate and filter water to obtain nutrition are very different
from springsnails that crawl on the substrate and scrape periphyton
(various forms of algae and diatoms) off the substrate. Unfortunately,
very little research has been done specifically on the effects of
contaminants on springsnails and mussels are one of the most closely
related groups available for comparison. However, this reference has
been removed from this final rule.
(10) Comment: The relevance of South Spring River is not apparent
in your discussion of Noel's amphipod. The South Spring River has been
dry for many years.
Our Response: The discussion of Noel's amphipod and the dry South
Spring River was included to document that this previously known
population has likely been extirpated.
(11) Comment: Are crayfish known predators of springsnails?
Our Response: Crayfish are known to consume aquatic macrophytes and
algae that springsnails rely on for grazing and egg laying (Service
2004b). In addition, crayfish have been cited as a threat and are known
to directly prey upon aquatic invertebrates such as springsnails (e.g.,
Three Forks springsnail (Pyrgulopsis trivialis)) (Arizona Game and Fish
Department 2003; Service 2004b). Nevertheless, we have not observed any
crayfish within habitat occupied by
[[Page 46308]]
these four invertebrates, with the exception of Diamond Y Springs
Complex where an undescribed native crayfish occurs. See also ``Factor
C'' under the ``Summary of Factors Affecting the Species'' section
below.
(12) Comment: Effects to these species from prolonged drought,
nutrient enrichment, and sedimentation are all unsubstantiated.
Our Response: There is no doubt that prolonged drought leading to
spring diminishment or drying would have a negative impact on the
invertebrates. Little research has been done specifically on
springsnails to document their response to elevated nutrients,
contaminants, or sedimentation. However, based on biological principles
and effects observed in other related invertebrates, we can draw
reasonable conclusions about what we would expect to happen to these
species.
(13) Comment: Have surveys for these species been conducted at
Bottomless Lakes State Park?
Our Response: Surveys were conducted on Bottomless Lakes State Park
during the 1990s by the NMDGF and during the 1980s by D.W. Taylor.
Perennial sinks west-northwest of Lea Lake and its outflow to the
south, which eventually flows to the BLM Overflow Wetlands, were also
surveyed for these invertebrates (Lang 2005). Although potentially
suitable habitat for the four invertebrates is available at Bottomless
Lakes State Park, these surveys failed to document their occurrence
(New Mexico Energy Minerals and Natural Resources Department 2000;
NMDGF 2005b).
(14) Comment: A new population of Noel's amphipod has been recently
discovered on BLNWR.
Our Response: The commenter is correct. Noel's amphipod currently
persists on BLNWR at the Sago Spring wetland complex (including
Sinkhole No. 31), Bitter Creek, and along the western boundary of Area
6, in the west ditch along Area 7, and along the northwest fenceline of
Hunter Marsh (NMDGF 2005c). A new population was discovered in 2004 in
a spring belonging to the City of Roswell that borders BLNWR. This
population is included in the listing portion of this final rule, but
is not within the designation of critical habitat. The critical habitat
designation does not include these private lands because section
4(b)(4) of the Act and the Administrative Procedure Act (5 U.S.C. 551
et seq.) requires that areas designated as critical habitat must first
be proposed as such. Thus, we cannot make additions in this final rule
to include areas that were not included in the proposed rule.
Designation of such areas would require a new or revised proposal and
subsequent final rule. Should critical habitat be considered in the
future for the Noel's amphipod, we will consider this area in any such
determination.
(15) Comment: The ongoing drought appears to be more of a threat to
these species than groundwater pumping.
Our Response: We agree. Please refer to the ``Summary of Factors
Affecting the Species'' for further discussion of this issue.
(16) Comment: The proposed rule lacks documentation of groundwater
or surface contamination threats to the four invertebrates.
Our Response: Based upon public comments and information received,
we have updated our analysis to include our current understanding of
the threats from groundwater or surface contamination to the four
invertebrates. Please see the ``Summary of Factors Affecting the
Species'' section.
(17) Comment: The Pleistocene Era was mentioned several times in
the proposed rule. Does the Service intend to recover these species to
levels that were present during this historic era?
Our Response: No, section 4 of the Act and its implementing
regulations (50 CFR part 424) set forth the procedures for adding
species to the List of Endangered and Threatened Wildlife and Plants. A
species may be determined to be endangered or threatened due to one or
more of the five factors described in section 4(a)(1) of the Act. As
detailed below in our analysis, we examine the listing factors and
their application to the four invertebrates. The discussion of these
species in relation to the Pleistocene Era was presented as evidence of
an apparent historical decline in the numbers, range, and distribution.
We did not intend to suggest that the four invertebrates need to be
restored to Pleistocene Era levels to be considered recovered.
(18) Comment: Is there a plan to control introduced or exotic
snails or other species that may prey upon or compete with the four
invertebrates?
Our Response: BLNWR is managed for wildlife conservation, which
includes restoration and maintenance of biological integrity,
diversity, and environmental health. Major land management activities
on BLNWR include water level management in impoundments to provide
habitat for waterfowl, shorebirds, and other groups of species, habitat
restoration, prescribed burning, control of saltcedar, and management
of noxious weeds (Service 2005a). Management or removal of exotic
species that compete with these invertebrates will be evaluated in the
development of a recovery plan, but this management is currently
conducted as appropriate. For example, removal of non-native fishes
from Diamond Y Springs Complex using antimycin, netting, and trapping
was conducted in the past for conservation of Leon Springs pupfish
(Service 2005a). For further information and analysis concerning exotic
species, please refer to the ``Factor C'' under the ``Summary of
Factors Affecting the Species'' section.
Issue 2: Procedural and Legal Compliance
(19) Comment: In the proposed rule for the four invertebrate
species, restrictions are proposed on groundwater pumping within the
Pecos Basin, which would have serious effects on the water supply and
use of water by the citizens of New Mexico.
Our Response: We disagree, the proposed rule did not propose
restrictions on groundwater pumping. Consistent with our Interagency
Cooperative Policy for Endangered Species Act Section 9 Prohibitions,
published in the Federal Register on July 1, 1994 (59 FR 34272), we
identified in the proposed rule those activities that we believe would
or would not constitute a violation of the prohibitions identified in
section 9 of the Act. The final Federal listing of these four
invertebrates under the Act requires that Federal agencies consult with
the Service on activities involving Federal funding, a Federal permit,
Federal authorization,or other Federal actions. Consultation (under
section 7 of the Act) is required when activities have the potential to
affect the four invertebrates or designated critical habitat. The
consultation will analyze and determine to what degree the species are
impacted by the proposed action. Section 7 of the Act prohibits actions
funded, authorized, or carried out by Federal agencies from
jeopardizing the continued existence of a listed species or destroying
or adversely modifying the listed species' critical habitat. This final
Federal listing does not restrict groundwater pumping or any other
actions.
The environmental assessment found that spring flows within the
proposed critical habitat on BLNWR are already protected by existing
water rights afforded by the New Mexico Office of the State Engineer's
administration of the Roswell Basin. In 1967, water rights were
adjudicated in the Roswell Basin, wells were metered, and pumping rates
administered by the Office of the State Engineer (OSE). Currently, any
[[Page 46309]]
proposed change in use of water (underground or surface depletion) in
the Roswell Basin will undergo analysis by OSE to determine if there
would be impairment to existing water rights (McCord et al. 2005). The
OSE will not allow such change if it impairs the Federal water right in
any respect (NMISC 2005). Thus the spring flows on BLNWR should be
protected from any changes in groundwater pumping near the refuge in
the future.
In Texas, Pecos assiminea currently has no State or other
regulatory protection. Some protection for the habitat of this species
is provided with the ownership of the springs by TNC (Karges 2003).
Groundwater pumping that could affect spring flows is subject to
limited regulation in Texas. State agencies do not control groundwater
pumping, and Texas courts have held that, with few exceptions,
landowners have the right to take all the water that can be captured
under their land (rule of capture), regardless of impacts to neighbors
or natural resources. As noted in the economic analysis, within Texas
further hydrological studies are necessary to determine the impact of
groundwater pumping on surface and groundwater levels at Units 3 and 4.
The TNC has stated that additional research on the delineation of
watersheds is crucial to the sustainable, long-term conservation of the
springs. If hydrological studies determine a link between the various
aquifers, we would work with private landowners on a volunteer basis to
minimize impacts to the Pecos assiminea from groundwater withdrawals.
(20) Comment: The groundwater depletion analysis fails to rely upon
the best available science, does not utilize an accurate and reliable
model, and mischaracterizes effects of groundwater pumping.
Our Response: Based upon new information we received during the
comment periods, we revised our analysis from the proposed rule to
reflect our current understanding regarding the threat of groundwater
depletion on the four invertebrates and their habitat in New Mexico.
Please refer to the ``Summary of Factors Affecting Species'' section.
(21) Comment: The status of these species will not improve if they
are listed.
Our Response: Federal listing in and of itself does not improve the
status of the species. Listing these species authorizes the development
of a recovery plan. The recovery plan will likely identify both State
and Federal efforts for conservation of these species and establish a
framework for agencies and stakeholders to coordinate activities and
cooperate with each other in conservation efforts. The plan will set
recovery priorities and describe site-specific management actions
necessary to achieve conservation and survival of the four
invertebrates. See also response to comment 22 below for related
information about the five factors described in section 4(a)(1) of the
Act. Also note the discussion on section 7 consultation requirements in
our response to comment 19 above.
(22) Comment: Why does the Service want to list these four
invertebrates when they are already within protected areas?
Our Response: We have analyzed the threats to these species based
upon the five factors described in section 4(a)(1) of the Act. Although
these species occur on areas that are currently managed for
conservation purposes, we have determined based on our analysis of the
threats discussed below in the section ``Summary of Factors Affecting
the Species,'' that these four invertebrate species are in danger of
extinction throughout all or a significant portion of their respective
ranges. Our analysis determined that these species are threatened by
activities such as oil and gas production and development, groundwater
pumping, and introduction of non-native species that are beyond the
boundaries and/or the management protected areas where the species are
found. Thus, the four invertebrates meet the definition of endangered
species.
(23) Comment: If these species are listed, is there a possible
effect to the U.S. Bureau of Reclamation with respect to delivery of
irrigation water?
Our Response: Federal listing will require the Bureau of
Reclamation (Reclamation) to consult with us on activities that have
the potential to adversely affect the four invertebrates or designated
critical habitat. None of Reclamation's current projects will be
affected by the listing of the invertebrates and we are not aware of
any future projects that may be affected by the listing. Delivery of
irrigation water occurs via the Pecos River and we do not anticipate
that listing these species will affect that activity.
(24) Comment: Will the listing of these species impede the ability
of the State of New Mexico to meet Pecos Compact River obligations?
Our Response: No, the NMISC has been actively acquiring and leasing
water rights to meet the State's delivery obligations to Texas as
specified in the Pecos River Compact and pursuant to an Amended Decree
entered by the U.S. Supreme Court. For example, between 1991 and 1999,
$27.8 million was spent on the Pecos River water rights acquisition
program. We do not anticipate that the listing of these species or the
designation of critical habitat will alter the ability of the NMISC to
meet Pecos River Compact delivery obligations. The amount of water
being pumped from the Roswell Basin should not change; however, the use
of water will change. For example, instead of being applied to fields,
the water may be delivered to the Pecos River directly to meet Compact
delivery obligations.
(25) Comment: Will oil and gas exploration be further restricted in
areas designated as critical habitat?
Our Response: No, the Service does not anticipate that the
designation of critical habitat will restrict oil and gas exploration.
Section 7 consultation, when required, would analyze any impacts to the
species and their designated critical habitat. The environmental
assessment found that oil and gas projects with Federal involvement in
the BLNWR and the surrounding area are already subject to stipulations
for protecting groundwater (Service 2005). The Oil Conservation
Division of the New Mexico Energy, Minerals, and Natural Resources
Department regulates oil and gas well drilling and casing in part to
prevent contamination of groundwater (19 NMAC 15.3).
BLNWR is excluded from the designation of critical habitat for the
four invertebrate species, and critical habitat would not result in
additional section 7 consultations on federally supported oil and gas
projects. Oil and gas well development in the vicinity of Diamond Y
Springs Complex and East Sandia Spring occurs on private lands with no
Federal involvement. Therefore, section 7 consultations on the effects
to designated critical habitat would likely not occur for these
projects. For this reason, we do not believe there would be any
additional restrictions to oil and gas exploration activities.
Issue 3: National Environmental Policy Act (NEPA) Compliance and
Economic Analysis
(26) Comment: What has regulation or policy of Federal actions cost
State and County governments before listing and critical habitat
designation?
Our Response: Since the proposed listing of the four invertebrates
species, there have been specific conservation actions implemented that
have taken into account the protection of the species. An estimated
$366,000 to $494,000 in costs have been incurred by Federal and State
agencies for the four invertebrates (Service 2005b). These
[[Page 46310]]
costs are related to developing the New Mexico State recovery plan and
have included monitoring the four invertebrates' habitat, consultant
fees, staff time devoted to developing the plan, administrative costs
related to past conferences under section 7 of the Act, and associated
monitoring of invertebrate habitat. We did not find that County
governments have incurred any costs related to the conservation of
these species.
(27) Comment: Does the Service have an estimate of the costs
required to recover the four invertebrates?
Our Response: The costs of actions to recover the four
invertebrates will be estimated during the development of a recovery
plan.
(28) Comment: The economic analysis should consider benefits of the
critical habitat designation.
Our Response: In the context of a critical habitat designation, the
primary purpose of the rulemaking (i.e., the direct benefit) is to
designate areas that have the features on which the species depend and
that are in need of special management.
The designation of critical habitat may result in two distinct
categories of benefits to society: (1) Use benefits; and (2) non-use
benefits. Use benefits are simply the social benefits that accrue from
the physical use of a resource. Visiting critical habitat to see
endangered species in their natural habitat would be a primary example.
Non-use benefits, in contrast, represent welfare gains from ``just
knowing'' that a particular listed species'' natural habitat is being
specially managed for the survival and recovery of that species. Both
use and non-use benefits may occur unaccompanied by any market
transactions.
A primary reason for conducting an economic analysis is to provide
information regarding the economic impacts associated with a proposed
critical habitat designation. Section 4(b)(2) of the Act requires the
Secretary to designate critical habitat based on the best scientific
data available after taking into consideration the economic impact,
impact to national security, and any other relevant impact, of
specifying any particular area as critical habitat. Economic impacts
can be both positive and negative and by definition, are observable
through market transactions.
Where data are available, the economic analysis attempts to
recognize and measure the net economic impact of the proposed
designation. For example, if the fencing of a species' habitat to
restrict motor vehicles results in an increase in the number of
individuals visiting the site for wildlife viewing, then the analysis
would recognize the potential for a positive economic impact and
attempt to quantify the effect (e.g., impacts that would be associated
with an increase in tourism spending by wildlife viewers). In this
particular instance, however, the economic analysis did not identify
estimates or measures of positive economic impacts that could offset
some of the negative economic impacts analyzed earlier in this
analysis.
While the Act requires the Service to specifically consider the
economic impact of a designation, it does not require the Service to
explicitly consider any broader social benefits (or costs) that may be
associated with the designation. In fact, the Service believes that
this is by Congressional design, because the Act explicitly states that
it is the Federal government's policy to conserve all threatened and
endangered species and the ecosystems upon which they depend. While
section 4(b)(2) of the Act gives the Secretary discretion to exclude
certain areas from the final designation, she is authorized to do so
only if an exclusion does not result in the extinction of the species.
Thus, the Service believes that explicit consideration of broader
social values for the species and its habitat, beyond economic impacts,
is not necessary as Congress has already clarified the importance our
society places on conserving all threatened and endangered species and
their natural habitats upon which they depend. In terms of carrying out
its responsibilities under section 4(b)(2) then, the Service need only
consider whether the economic impacts (both positive and negative) are
significant enough to merit exclusion of any particular area without
causing the species to go extinct.
(29) Comment: The economic analysis overstates costs by including
past costs that occurred before the species was listed, costs that
would result from the listing alone, and costs that derive from
conservation efforts for other listed species. Similarly, the economic
analysis includes costs of consultation with the Environmental
Protection Agency (EPA) regarding Concentrated Animal Feeding
Operations (CAFOs), which should be primarily associated with other
listed species, and the listing of the four invertebrates, and not
critical habitat designation.
Our Response: This analysis identifies those economic activities
believed to most likely threaten the four invertebrates and their
habitat and, where possible, quantifies the economic impact to avoid,
mitigate, or compensate for such threats within the boundaries of the
critical habitat determination. The economic analysis considers past
impacts associated with species conservation efforts that have been
incurred since the proposed listing and critical habitat determination
in 2002. The impact of these efforts is considered relevant to
understanding the potential impact of the listing and critical habitat
determination. Further, due to the difficulty in making a distinction
between listing and critical habitat effects within critical habitat
boundaries, this analysis considers all future conservation-related
impacts to be coextensive with the designation.
The consideration of co-extensive costs was mandated by the 10th
Circuit Court of Appeals ruling in the New Mexico Cattle Growers
Association case (248 F.3d at 1285), which directed us to consider all
impacts, ``regardless of whether those impacts are attributable co-
extensively to other causes.'' As explained in the economic analysis,
due to possible overlapping regulatory schemes and other reasons, there
are also some elements of the analysis which may overstate some costs.
Conversely, the 9th Circuit has recently ruled (``Gifford
Pinchot,'' 378 F.3d at 1071) that the Service's regulations defining
``adverse modification'' of critical habitat are invalid because they
define adverse modification as affecting both survival and recovery of
a species. The Court directed us to consider that adverse modification
should be focused on impacts to recovery. While we have not yet
proposed a new definition for public review and comment, changing the
adverse modification definition to respond to the Court's direction may
result in additional costs associated with critical habitat definitions
(depending upon the outcome of the rulemaking).
As described in section 1.2 of the economic analysis, coextensive
effects may also include impacts associated with overlapping protective
measures of other Federal, State, and local laws that aid habitat
conservation in the areas proposed for designation, including
protections for other listed species. These measures may be in part
precipitated by the consideration of the presence of the species and
impending critical habitat determination. Because the quantified
habitat conservation efforts, regardless of their primary impetus,
afford protection to the four invertebrates, they likely contribute to
the efficacy of the critical habitat determination efforts. The impacts
of these actions are therefore considered relevant for understanding
the full effect of the proposed critical habitat determination.
Enforcement actions
[[Page 46311]]
taken in response to violations of the Act, however, are not included.
(30) Comment: The economic analysis inappropriately includes costs
of delays in proposed drilling operations associated with industry
appeals on applications for drilling permits. The oil and gas industry,
however, is appealing environmental protections associated with their
permits and burdening themselves. This should not be included as a cost
of the critical habitat designation.
Our Response: Industry appeals regarding drilling applications are
a result of the implementation of environmental regulations, including
the Act, that recommend additional species and habitat conservation
efforts be undertaken with the drilling activity. The economic impacts
of these delays are therefore considered relevant in understanding the
impact of conservation efforts for the four invertebrates.
(31) Comment: It is unclear from the economic analysis what
additional protections from oil and gas activities may be provided by
the Service for the four invertebrates as the economic analysis
includes costs associated with the listing and with protections for
other species, but no additional costs associated specifically with the
critical habitat designation.
Our Response: This analysis identifies the types of modifications
to economic activities that may be undertaken to avoid, mitigate, or
compensate for threats to the species and habitat. The draft economic
analysis acknowledges the difficulty in distinguishing between listing
and critical habitat effects and therefore considers all future
conservation-related impacts to be coextensive with the critical
habitat designation. Further, the relative level to which multiple
considerations, including that of other species, contribute to the
undertaking of a conservation effort is unclear. The impacts quantified
in the analysis are assumed to be in some part precipitated by the
critical habitat designation for the four invertebrates. Absent
information on the specific increment by which critical habitat
designation contributes to the undertaking of these efforts, the total
impact of the effort is quantified, and not a fraction solely due to
critical habitat designation.
(32) Comment: The draft economic analysis relies on information
provided by impacted industries to quantify the costs to those
industries. These costs are inflated. For example, environmentally
protective project modifications such as closed-loop systems can result
in cost savings to the oil and gas industry. The draft economic
analysis, however, only includes the costs to the industry of modifying
projects to incorporate conservation measures for the species.
Our Response: As the commenter notes, the potential for cost
savings associated with implementing environmentally protective
technologies, such as closed-loop systems, is acknowledged in the draft
economic analysis on page 4-7. However, the level of benefit these
modifications may generate is unclear. Additionally, application of
closed-loop systems is not ubiquitous. As the industry indicates, it is
not always the most beneficial operations alternative. The draft
economic analysis therefore includes the full cost of this modification
to oil and gas operations as a high-end estimate of the impact of
conservation efforts.
(33) Comment: The NMDGF's 2004 Biennial Review of threatened and
endangered species in the State indicated that off-refuge land use
practices within areas of the Roswell Artesian Basin (RAB), such as
regional groundwater pumping for agriculture, municipal water supplies,
and the oil and gas industries, threaten the invertebrate species. In
contrast, a recent report prepared by the New Mexico Office of the
State Engineer (OSE) provides the most recent information regarding the
hydrology of the RAB. The report concludes that ``* * * an extended,
extreme drought, and not groundwater depletion through human activity,
would potentially threaten the future supply of water for the proposed
critical habitat located within the BLNWR.''
Our Response: Paragraph 77 and section 4.2.2 of the draft economic
analysis state that no hydrologic models currently exist to determine
the impact of groundwater pumping of the RAB on the springs at the
BLNWR. The revised economic analysis acknowledges recent information
resulting from the OSE report. As the draft economic analysis does not
quantify impacts of critical habitat designation to groundwater
pumping; however, the quantitative results of this analysis are
unchanged as a result of this comment.
Summary of Changes From the Proposed Rule
Based upon our review of the public comments, the economic
analysis, environmental assessment, issues addressed at the public
hearing, and any new relevant information that may have become
available since the publication of the proposal, we reevaluated our
proposed listing and critical habitat designation and made changes as
appropriate. Other than minor clarifications and incorporation of
additional information on the species' biology, this final rule differs
from the proposal by:
(1) The exclusion of critical habitat on BLNWR because special
management considerations are currently provided to the four
invertebrates through current BLNWR management; and
(2) Changes to the primary constituent elements of critical habitat
for the Pecos assiminea.
Summary of Factors Affecting the Species
Section 4 of the Act and implementing regulations (50 CFR 424) set
forth the procedures for adding species to the Federal lists. A species
may be determined to be threatened or endangered due to one or more of
the five factors described in section 4(a)(1) of the Act. These factors
and their application to the Roswell springsnail, Koster's springsnail,
Pecos assiminea, and Noel's amphipod are as follows.
A. The present or threatened destruction, modification, or
curtailment of its habitat or range.
Several biological traits of a population have been identified as
putting a species at risk of extinction (McKinney 1997; O'Grady 2004).
Some of these characteristics include having a localized range, limited
mobility, and fragmented habitat (McKinney 1997; O'Grady 2004). The
four invertebrates have all of these characteristics. Having a small,
localized range means that any perturbation, either natural (e.g.,
drought) or anthropogenic (e.g., water contamination) can eliminate
many or all of the existing populations. Having a high number of
individuals at a site provides no protection against extinction. Noel
(1954) noted that the amphipod in Lander Spring was the most abundant
animal present. It was extirpated from that site when the spring dried
up (Cole 1985). The range reduction trend in these snail species (e.g.,
by extirpation of once widely distributed but localized populations) is
supported by the Pleistocene fossil record in conjunction with re-
inventory of known site occurrences in which no individuals were
detected (Noel 1954; Taylor 1987; Mehlhop 1992, 1993; NMDGF 1999).
Fossil records indicate that at least one or more of these snail
species were historically found at Berrendo Creek, North Spring, and
South Spring Rivers, and along the Pecos River (NMDGF 1999). This
evidence suggests an apparent historical decline in the numbers, range,
and distribution of these species.
[[Page 46312]]
Limited mobility restricts the ability of the invertebrates to find
and disperse to other suitable habitats or to move out of habitat that
becomes unsuitable. Consequently, their range remains restricted and
they are unable to avoid contaminants or other unfavorable changes to
their habitat. Fragmented (unconnected) habitat restricts gene flow
among populations and limits the ability of the invertebrates to
recolonize habitats that have been disturbed but then recover. For
example, three springs once contributed to Berrendo Creek in the
Roswell Basin. If the population of springsnails in one of the springs
was eliminated because of a toxic spill, after the habitat had
recovered, the spring could have been colonized naturally by dispersal
of animals from the other springs. In the currently fragmented
habitats, dispersal is highly unlikely and if a population is
extirpated the habitat probably will not be recolonized, further
restricting the range.
In addition to the characteristics listed above that may put
species at greater risk of extinction, habitat loss, introduced
species, and habitat degradation can also lead to extinction (Meffe et
al. 1994; Frankham et al. 2002). Each of these topics is discussed in
detail. Curtailment of range and habitat of the four invertebrates has
occurred primarily through the loss of suitable spring habitat. These
species were most likely much more widely distributed throughout the
Pecos River Basin during the wetter climatic period of the Pleistocene.
As the climate became warmer and drier, the invertebrates were
restricted to the remaining free-flowing springs. Fossil records
indicate that two of the snail species were found at Berrendo Creek and
along the Pecos River (Taylor 1987).
In addition, in the late 1800s, flow at North Spring, South Spring,
and Berrendo Creek was 85 cubic feet per second (cfs) (2.4 cubic meters
per second [cms], 60 cfs (1.7 cms), and 66 (1.9 cms) cfs, respectively
(Fiedler and Nye 1933). These systems each provided abundant habitat
for the invertebrates. Lander Spring, a tributary spring of South
Spring, harbored Noel's amphipod (Noel 1954). The historic connection
of these spring systems to the Pecos River most likely facilitated
dispersal of the invertebrates throughout the basin downstream of this
area.
In the 1880s, irrigated agriculture in the Roswell and Artesia
Basins was limited to a few small farms (Fielder and Nye 1933). By the
end of 1905, 485 artesian wells had been drilled and by 1927, 1,424
wells were pumping water (Fiedler and Nye 1933). One well, drilled for
the Oasis Cotton Company, is estimated to have produced 9,000 gallons/
minute (20 cfs) (Fiedler and Nye 1933, Jones and Balleau 1996). As a
result of extensive groundwater pumping, the artesian head in the basin
declined (Fiedler and Nye 1933). The amount of decline depended on
location within the basin and ranged from 32 to 204 feet (9.7 to 62.2
meters) from original levels by 1927, and led to a decrease in area
within the basin that had artesian flow (Fiedler and Nye 1933).
Groundwater depletion continued until the mid-1970s, when it reached
its maximum (McCord et al. 2005).
By 1926, South Spring was dry (Jones and Balleau 1996). Berrendo
Spring still produced 8.3 cfs, about 12 percent of the original 1880s
flow (Jones and Balleau 1996). Today, Berrendo Well produces less than
1 cfs (McCord et al. 2005). Lander Spring went dry in the late 1950s or
early 1960s (Cole 1981), extirpating the population of Noel's amphipod,
which in the early 1950s had been described by Noel (1954) as the most
abundant animal in the spring. Discharge at North Spring is unknown.
Jones and Balleau (1996) list its flow as 0 in 1926, but Cole (1981)
described 3 small separate brooks that entered a pond on a private golf
course in 1967. Surveys in 1995 at the site indicated that Roswell
springsnail and Koster's springsnail were still present at the location
(Noel's amphipod once occupied the site). Surveys in 2004 found none of
the species, most likely due to habitat modification from pond
enlargement (NMDGF 2005a). Surface flow at BLNWR was also diminished by
artesian pumping. Springs adjacent to Salt Creek no longer flow, and
surface flow from the Middle Area of BLNWR (sum of flow in upper Bitter
Creek and Middle Area springs) was 15 cfs (0.4 cms)