Endangered and Threatened Wildlife and Plants; 12-Month Finding on a Petition To List Texas Fatmucket, Golden Orb, Smooth Pimpleback, Texas Pimpleback, and Texas Fawnsfoot as Threatened or Endangered, 62166-62212 [2011-25471]
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Federal Register / Vol. 76, No. 194 / Thursday, October 6, 2011 / Proposed Rules
Gary
Mowad, Texas State Administrator, U.S.
Fish and Wildlife Service
Fish and Wildlife Service (see
ADDRESSES); by telephone at 512–927–
50 CFR Part 17
3557; or by facsimile at 512–927–3592.
If you use a telecommunications device
[FWS–R2–ES–2011–0079; MO 92210–0–0008 for the deaf (TDD), please call the
B2]
Federal Information Relay Service
(FIRS) at 800–877–8339.
Endangered and Threatened Wildlife
SUPPLEMENTARY INFORMATION:
and Plants; 12-Month Finding on a
Petition To List Texas Fatmucket,
Background
Golden Orb, Smooth Pimpleback,
Section 4(b)(3)(B) of the Act (16
Texas Pimpleback, and Texas
U.S.C. 1531 et seq.) requires that, for
Fawnsfoot as Threatened or
any petition to revise the Federal Lists
Endangered
of Endangered and Threatened Wildlife
and Plants that contains substantial
AGENCY: Fish and Wildlife Service,
scientific or commercial information
Interior.
that listing the species may be
ACTION: Notice of 12-month petition
warranted, we make a finding within 12
finding.
months of the date of receipt of the
petition. In this finding, we will
SUMMARY: We, the U.S. Fish and
determine that the petitioned action is:
Wildlife Service (Service), announce a
(1) Not warranted, (2) warranted, or (3)
12-month finding on a petition to list
warranted, but the immediate proposal
five mussel species in Texas as
of a regulation implementing the
threatened or endangered and to
petitioned action is precluded by other
designate critical habitat under the
pending proposals to determine whether
Endangered Species Act of 1973, as
species are threatened or endangered,
amended (Act). The five species are
and expeditious progress is being made
Texas fatmucket (Lampsilis bracteata),
to add or remove qualified species from
golden orb (Quadrula aurea), smooth
the Federal Lists of Endangered and
pimpleback (Q. houstonensis), Texas
Threatened Wildlife and Plants. Section
pimpleback (Q. petrina), and Texas
4(b)(3)(C) of the Act requires that we
fawnsfoot (Truncilla macrodon). After
treat a petition for which the requested
review of all available scientific and
action is found to be warranted but
commercial information, we find that
precluded as though resubmitted on the
listing these five mussel species is
date of such finding, that is, requiring a
warranted. Currently, however, listing
subsequent finding to be made within
of these species is precluded by higher
12 months. We must publish these 12priority actions to amend the Federal
month findings in the Federal Register.
Lists of Endangered and Threatened
Wildlife and Plants. Upon publication
Previous Federal Actions
of this 12-month petition finding, we
This 12-month petition finding covers
will add these five species to our
five species of mussels that are grouped
candidate species list. We will develop
together because of their overlapping or
a proposed rule to list these species as
proximate ranges within the river basins
our priorities allow. We will make any
of central Texas. The petitions for listing
determination on critical habitat during
these five species were parts of two
development of the proposed listing
multi-species petitions, dated June 18,
rule. In any interim period, we will
2007, and October 9, 2008. The other
address the status of the candidate taxa
species from those petitions, including
through our annual Candidate Notice of
other Texas mussels, will be considered
Review.
in separate petition findings.
DATES: The finding announced in this
On June 25, 2007, we received a
document was made on October 6, 2011. formal petition dated June 18, 2007,
from Forest Guardians (now WildEarth
ADDRESSES: This finding is available on
Guardians), requesting that we: (1)
the Internet at https://
Consider all full species in our
www.regulations.gov at Docket Number
Southwest Region ranked as G1 or G1G2
FWS–R2–ES–2011–0079. Supporting
by the organization NatureServe, except
documentation we used in preparing
those that are currently listed, proposed
this finding is available for public
for listing, or candidates for listing; and
inspection, by appointment, during
(2) List each species as either threatened
normal business hours at the U.S. Fish
or endangered with critical habitat. The
and Wildlife Service, 1505 Ferguson
petitioned group of species included
Lane, Austin, TX 78754. Please submit
four Texas mussels, two of which are
any new information, materials,
comments, or questions concerning this included in this finding: the Texas
fatmucket and golden orb. Two
finding to the above address.
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DEPARTMENT OF THE INTERIOR
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additional mussels from eastern Texas,
the Texas heelsplitter (Potamilus
amphichaenus) and Salina mucket (P.
metnecktayi), were also included in this
petition. The petition incorporated all
analyses, references, and documentation
provided by NatureServe in its online
database at https://www.natureserve.org/
into the petition. Included in
NatureServe was supporting
information regarding the species’
taxonomy and ecology, historical and
current distribution, present status, and
actual and potential causes of decline.
We sent a letter dated July 11, 2007, to
Forest Guardians acknowledging receipt
of the petition and stating that the
petition was under review by staff in
our Southwest Regional Office.
On October 15, 2008, we received a
petition dated October 9, 2008, from
WildEarth Guardians, requesting that
the Service list as threatened or
endangered and designate critical
habitat for six species of freshwater
mussels, including the smooth
pimpleback, Texas pimpleback, and
Texas fawnsfoot. Two additional
mussels from the Rio Grande basin, the
false spike (Quincuncina mitchelli) and
Mexican fawnsfoot (Truncilla congata),
were also included in this petition. In
addition to other information, the
petition incorporated all analyses,
references, and documentation provided
by NatureServe in its online database at
https://www.natureserve.org/. In a
November 26, 2008, letter to the
petitioner, we acknowledged receipt of
the second petition and stated that the
petition for the six mussel species was
under review by staff in our Southwest
(Region 2) and Southeast (Region 4)
Regional Offices. The southern
hickorynut (Obovaria jacksoniana) was
also included in this 2008 petition, and
on March 23, 2010 (75 FR 13717), we
found that the petition did not present
substantial information supporting that
that species may be endanagered or
threatened.
On December 15, 2009, we published
our 90-day finding that the petitions
presented substantial scientific
information indicating that listing nine
Texas mussels may be warranted (74 FR
66260). As a result of the finding, we
initiated a status review for all nine
species. This notice constitutes the 12month finding on the June 18, 2007,
petition to list the Texas fatmucket and
golden orb and the October 9, 2008,
petition to list the smooth pimpleback,
Texas pimpleback, and Texas fawnsfoot
as threatened or endangered. Our
petition findings for the remaining
Texas mussel species will be published
at a later time.
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with a discussion of the priority and
progress of our listing actions.
Review of Status Based on Five Factors
Section 4 of the Act (16 U.S.C. 1533)
and implementing regulations (50 CFR
part 424) set forth procedures for adding
species to, removing species from, or
reclassifying species on the Federal
Lists of Endangered and Threatened
Wildlife and Plants. Under section
4(a)(1) of the Act, a species may be
determined to be endangered or
threatened based on any of the
following five factors:
(A) The present or threatened
destruction, modification, or
curtailment of its habitat or range;
(B) Overutilization for commercial,
recreational, scientific, or educational
purposes;
(C) Disease or predation;
(D) The inadequacy of existing
regulatory mechanisms; or
(E) Other natural or manmade factors
affecting its continued existence.
In making these findings, we discuss
below information pertaining to each
species in relation to the five factors
provided in section 4(a)(1) of the Act. In
considering what factors might
constitute threats to a species, we must
look beyond the exposure of the species
to a particular factor to evaluate whether
the species may respond to the factor in
a way that causes actual impacts to the
species. If there is exposure to a factor
and the species responds negatively, the
factor may be a threat, and during the
status review, we attempt to determine
how significant a threat it is. The threat
is significant if it drives or contributes
to the risk of extinction of the species
such that the species warrants listing as
endangered or threatened as those terms
are defined by the Act. However, the
identification of factors that could
impact a species negatively may not be
sufficient to compel a finding that the
species warrants listing. The
information must include evidence
sufficient to suggest that the potential
threat has the capacity (i.e., it should be
of sufficient magnitude and extent) to
affect the species’ status such that it
meets the definition of endangered or
threatened under the Act.
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Summary of Procedures for Determining
the Listing Status of Species
General Mussel Biology
All five species are freshwater
mussels in the family Unionidae and
occur only in Texas, in portions of the
Colorado, Guadalupe, Nueces-Frio, and
Brazos River systems (Howells et al.
1996, p. 1). Adult freshwater mussels
are suspension feeders, drawing in food
and oxygen through their incurrent
siphon (tube that draws water into the
shell). They may also feed on organic
particles in sediment using the large,
muscular foot (an organ used to anchor
the mussel in the substrate or for
locomotion) (Raikow and Hamilton
2001, p. 520). Adults feed on algae,
bacteria, detritus (dead organic
material), microscopic animals, and
dissolved organic matter (Fuller 1974,
pp. 221–222; Silverman et al. 1997, p.
1862; Nichols and Garling 2000, pp.
874–876; Christian et al. 2004, p. 109).
For their first several months, as they
inhabit interstitial spaces (small spaces
between sediment particles) within the
substrate, juvenile mussels feed using
cilia (fine hairs) on the foot to capture
suspended as well as depositional
material, such as algae and detritus
(Yeager et al. 1994, pp. 253–259).
Mussels tend to grow relatively rapidly
for the first few years, and then slow
appreciably at sexual maturity, when
energy presumably is being diverted
from growth to reproductive activities
(Baird 2000, pp. 66–67).
As a group, mussels are extremely
long lived, living from two to several
decades (Rogers et al. 2001, p. 592), and
possibly up to 200 years in extreme
instances (Bauer 1992, p. 427). Most
mussel species, including the five in
this finding, have distinct forms of
males and females. During
reproduction, males release clouds of
sperm into the water column, which
females draw in through their siphons.
Fertilization takes place internally, and
the resulting eggs develop into
specialized larvae (called glochidia)
within the female gills. The females
release matured glochidia individually,
in small groups, or embedded in larger
mucus structures called conglutinates.
The glochidia of freshwater mussels
are obligate parasites (cannot live
independently of their hosts) on the
gills or fins of fishes (Vaughn and
Taylor 1999, p. 913). Glochidia die if
they fail to find a host fish, attach to a
fish that has developed immunity from
prior infestations, or attach to the wrong
location on a host fish (Neves 1991, p.
254; Bogan 1993, p. 299). Glochidia
encyst (enclose in a cyst-like structure)
on the host’s tissue and develop into
Evaluation of the Status of Each of the
Five Mussel Species
In this finding, we first provide a
description of general mussel biology.
Then, for each of the five species, we
describe the species, its life history, and
habitat; evaluate listing factors for that
species; and present our finding that the
petitioned action is warranted or not for
that species. We follow these
descriptions, evaluations, and findings
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juvenile mussels weeks or months after
attachment (Arey 1932, pp. 214–215).
Mussels experience their primary
opportunity for dispersal and movement
within the stream as glochidia attached
to a host fish (Smith 1985, p. 105). Upon
release from the host, newly
transformed juveniles drop to the
substrate on the bottom of the stream.
Those juveniles that drop in unsuitable
substrates die because their immobility
prevents them from relocating to more
favorable habitat. Juvenile freshwater
mussels burrow into interstitial
substrates and grow to a larger size that
is less susceptible to predation and
displacement from high flow events
(Yeager et al. 1994, p. 220). Throughout
the rest of their life cycle, mussels
generally remain within the same small
area where they released from the host
fish.
Species Information for Texas
Fatmucket
Species Description
The Texas fatmucket is a large,
elongated mussel that reaches a
maximum length of 100 millimeters
(mm) (3.94 inches (in)) (Howells 2010c,
p. 2). The shell is oval to elliptical or
somewhat rhomboidal and tan to
greenish-yellow with numerous
irregular, wavy, and broad and narrow
dark brown rays, with broad rays
widening noticeably as they approach
the ventral (underside) margin. The
nacre (inside of the shell) is white with
occasional yellow or salmon coloration
and iridescent posteriorly (Howells
2010c, p. 2). Females have mantle flaps
(extensions of the tissue that covers the
visceral mass) that often resemble
minnows, including eye spots, lateral
line, and fins (Howells 2010c, p. 2).
Taxonomy
The Texas fatmucket was first
described in 1855 by Gould as Unio
bracteatus and later moved to the genus
Lampsilis by Simpson (1900, p. 543).
Some forms found in headwater streams
were historically split into a different
species, L. elongatus, but they have
since been determined to be
ecophenotypes (individuals whose
shape is determined by their
environment) of L. bracteata (Howells
2010c, p. 5). The Texas fatmucket is
recognized by the Committee on
Scientific and Vernacular Names of
Mollusks of the Council of Systematic
Malacologists, American Malacological
Union (Turgeon et al. 1998, p. 34), and
we recognize it as a valid species.
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Biology and Life History
Although there is no specific
information on age and size of maturity
of the Texas fatmucket, it is likely
similar to a related species, the
Louisiana fatmucket (L. hydiana), which
reaches sexual maturity around 36 mm
(1.4 in) (Howells 2000b, pp. 35–48;
Howells 2010c, p. 3). Texas fatmucket
females have been found gravid (with
glochidia in the gill pouch) from July
through October, although brooding
may continue throughout much of the
year (Howells 2010c, p. 3). Texas
fatmucket females display a mantle lure
to attract host fish, releasing glochidia
when the lure is bitten or struck by the
fish. Bluegill (Lepomis macrochirus)
and green sunfish (L. cyanellus) have
been successful hosts in laboratory
studies (Howells 1997b, p. 257). Hosts
such as these sunfishes are common,
widely distributed species in Texas that
occur in an array of habitat types (Hubbs
et al. 2008, p. 45) and would not
generally be expected to be a limiting
factor in Texas fatmucket reproduction
and distribution (Howells 2010c, p. 3).
Habitat
The Texas fatmucket occurs in
moderately sized rivers in mud, sand, or
gravel, or mixtures of these substrates
(Howells 2010c, p. 4) and sometimes in
narrow crevices between bedrock slabs
(Howells 1995, p. 21). Live individuals
have been found in relatively shallow
water, rarely more than 1.5 meters (m)
(4.9 feet (ft)) deep, and usually less.
Remaining populations typically occur
at sites where one or both banks are
relatively low, allowing floodwaters to
spread out over land and thereby
reducing damage from scouring
(Howells 2010c, p. 4). The species does
not occur in ponds, lakes, or reservoirs,
suggesting that it is intolerant of deep,
low-velocity water created by artificial
impoundments.
Distribution and Abundance
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Historical Distribution
The Texas fatmucket historically had
populations in at least 18 rivers in the
upper Colorado, Guadalupe, and San
Antonio River systems in the Texas Hill
Country and east-central Edwards
Plateau region of central Texas. In the
Colorado River, it ranged from Travis
County upstream approximately 320
kilometers (km) (200 miles (mi)) to
Runnels County in the Colorado River.
It was also found in many tributaries,
including the Pedernales, Llano, San
Saba, and Concho Rivers, and Jim Ned,
Elm, and Onion Creeks (Howells et al.
1996, p. 61).
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In the Guadalupe-San Antonio River
basin, the Texas fatmucket occupied
approximately 240 km (150 mi) of the
Guadalupe River, from Gonzales County
upstream to Kerr County, including the
North Guadalupe River, Johnson Creek,
and the Blanco River. In the San
Antonio River, it ranged from its
confluence with the Medina River in
Bexar County upstream to the City of
San Antonio, as well as in the Medina
River and Cibolo Creek (Howells et al.
1996, p. 61; Howells 2010c, p. 6).
Strecker (1931, pp. 66–68) reported
Texas fatmucket from a lake in Victoria
County in the lower Guadalupe River
drainage (Howells 2010c, p. 6), but this
is probably a misidentified Louisiana
fatmucket, which occurs in lakes or
impoundments. A Salado Creek record
from Bell County (Strecker 1931, pp.
62–63) is also probably a misidentified
Louisiana fatmucket, since the Texas
fatmucket is not known to occur in the
Brazos River basin or its western
tributaries (Howells et al. 1996, p. 61;
Howells 2010c, p. 6).
Current Distribution
Based on historical and current data,
the Texas fatmucket has declined
significantly rangewide and is now
known from only nine streams in the
Colorado and Guadalupe River systems
in very limited numbers. All existing
populations are represented by only one
or two individuals and are likely not
stable or recruiting (juvenile mussels
joining the adult population). In the
streams where the species is extant
(surviving), populations are highly
fragmented and restricted to short
reaches with few exceptions. The Texas
fatmucket has been considered a species
of special concern by some
malacologists for several decades
(Athearn 1970, p. 28).
Colorado River System
The Texas fatmucket was historically
known to occur throughout the
Colorado River and numerous
tributaries (Randklev et al. 2010c, p. 4).
However, in the mainstem Colorado
River, the Texas fatmucket has not been
found, live or dead, in several decades
despite numerous surveys (Howells
1994, p. 4; 1995, pp. 20–21, 25, 29;
1996, pp. 20, 23; 1997a, pp. 27, 31, 34–
35; 1998, p. 10; 1999, p. 18; 2000a, pp.
25–27; 2002a, pp. 6–7; 2004, pp. 7, 10–
11; 2005, p. 6; Johnson 2009, p. 1;
Burlakova and Karatayev 2010a, p. 12),
and thus is considered extirpated
(eliminated from) from the Colorado
River mainstem. Within this system, the
species is only known from sparse
populations in Colorado River
tributaries, including the South Concho
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River, Spring Creek, Llano River
(including Threadgill Creek), Pedernales
River (including Live Oak Creek), Onion
Creek, Jim Ned Creek, Elm Creek, and
the San Saba River.
Evidence of persisting Texas
fatmucket populations has been found
in Spring Creek, a tributary to the
Middle Concho River, which flows into
the Concho River, a large tributary of the
Colorado River. Historically, Spring
Creek harbored Texas fatmucket in Irion
and Tom Green Counties (Randklev et
al. 2010c, p. 1). In 1993, discovery of
shell material prompted additional
surveys, and in 1997, one live
individual was found in Irion County
(Howells 1998, p. 13). Farther
downstream, in Tom Green County, two
live individuals were recorded in 1997,
upstream of Twin Buttes Reservoir
(Howells 1998, pp. 13–14), but no
evidence of this population was found
in 2008 (Burlakova and Karatayev
2010a, p. 12). Spring Creek was reported
to have dried in 1999 and 2000, which
may have eliminated the population
there (Howells et al. 2003, p. 5).
In the Llano River, there are three
areas that are currently known to
contain Texas fatmucket populations.
The species occurred throughout the
length of the river historically (Ohio
State University Museum (OSUM)
2011a, p. 1). A single shell was collected
in Llano County in 1992 (Howells 1994,
p. 6), and eight live individuals were
found in 2011 (Burlakova and Karatayev
2011, p. 1). Individuals were small in
size, indicating a potentially
reproducing population. The species
also persists in Mason County, where
two shell fragments of recently dead
Texas fatmucket were found in 1995
(Howells 1996, p. 22), and two live
individuals were collected at the same
site in 2009 (Burlakova and Karatayev
2010a, pp. 12–13). The species also
appears to persist in Kimble County,
where one live Texas fatmucket was
recorded in 2009 (Burlakova and
Karatayev 2010a, pp. 12–13).
In 2004, four live Texas fatmucket
were recorded from Threadgill Creek, a
tributary to the Llano River in Gillespie
and Mason Counties (Howells 2005, pp.
6–7). This population is on private land,
which limits survey access, but Howells
(2009, p. 5) indicates it likely persists
due to favorable land management.
Live Oak Creek, a tributary to the
Pedernales River in Gillespie County,
also contains a sparse Texas fatmucket
population. In 2002, 11 shells were
discovered, and in 2003, one live
individual was recorded, confirming the
species persisted in low numbers
(Howells 2003, p. 10; Howells 2004, pp.
8–9). Since that time, surveys have been
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conducted in Live Oak Creek on a fairly
regular basis. The stream was visited in
two different occasions in 2004, with
only shell material found (Howells
2005, pp. 7–8), and again in 2005, when
two live individuals were recorded
(Burlakova and Karatayev 2010a, p. 12).
The stream was surveyed in 2007 and
2008, but no evidence of the species was
found (Howells 2009, p. 5). This
population is presumed to be small but
persisting.
Original records of speckled
pocketbook (Lampsilis streckeri) from
Onion Creek in Travis County in 1931
are now believed to have been
misidentified; instead they represent
records of Texas fatmucket (Howells
2010c, p. 6; Randklev et al. 2010c, p. 4).
The stream was surveyed in 1993, and
no live freshwater mussels were found
(Howells 1995, p. 28). However, in
2010, several live Texas fatmucket were
found during a survey near Highway 71
(Groce 2011, pers. comm.), indicating
the species persists there.
Elm Creek, a tributary to the Colorado
River, has been known to harbor a Texas
fatmucket population since 1993, when
10 live individuals were recorded
(Howells 1995, p. 21). Since that time,
the population has declined, with two
individuals found in 1995 (Howells
1996, pp. 19–20), and no live
individuals found in 2001 or 2005
(Howells 2002a, p. 5; 2006, p. 63). In
2008, additional sites downstream of the
known population were surveyed and
one live individual was recorded after
15 person-hours of searching (Burlakova
and Karatayev 2010a, p. 12), indicating
that the species continues to persist in
Elm Creek, although in very low
numbers.
Texas fatmucket also persist in the
San Saba River, where the species has
been known to occur historically
(Randklev et al. 2010c, p. 2; OSUM
2011a, p. 1). The river was surveyed in
1997, and three live individuals were
found (Howells 1998, p. 16). In 2000
and 2004, no Texas fatmucket were
found in this stretch of river (Howells
2001, p. 29; Howells 2005, pp. 8–9). One
live individual was found in 2005
(Howells 2006, p. 64), and, in 2008, only
one shell of a recently dead individual
was found (Burlakova and Karatayev
2010a, p. 12). In 2005, the number of
mussels of all species collected was
about 40 percent of the 1997 numbers
(Howells 2006, p. 64), indicating an
overall decline in the freshwater mussel
fauna. Aquatic macrophyte (aquatic
plants larger than algae) abundance has
increased in this river, confounding
survey efforts and degrading mussel
habitat (Howells 2006, p, 64).
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Texas fatmucket have not been found
alive in the Pedernales River since 1978
(Howells 1999, p. 16). In 1992, a
thorough search of the habitat yielded
no live Texas fatmuckets, with only very
old dead shell material collected in the
banks above the normal high water line
(Howells 1994, p. 4). Because the
species was documented from Blanco
County by museum records (OSUM
2011a, p. 1), additional sections of the
river were also surveyed in 1992, with
no evidence of Texas fatmucket found,
although in 1993, very old Texas
fatmucket shell fragments were
discovered in Pedernales Falls State
Park (Howells 1995, p. 28). Mussel
habitat in this area is poor, and it is
unlikely the species persists there.
Subsequent searches of the river in 1998
yielded only dead shell material
(Howells 1999, p. 16).
The Texas fatmucket is considered
extirpated from the South Concho River
and Jim Ned Creek. In the South Concho
River, old Texas fatmucket shell
fragments were found in gravel bars in
Tom Green County in 1997, but there
has been no additional evidence of the
species (Howells 1998, p. 12).
Additionally, three live individuals
were recorded from Jim Ned Creek in
Brown County in 1979 (Randklev et al.
2010c, p. 3), but the species has not
been found in this stream since then
(Howells 1997a, pp. 29–30).
Guadalupe River System
While the Texas fatmucket was never
widely distributed in the Guadalupe
River system, the only remaining
populations are in the mainstem
Guadalupe River and possibly the North
Fork Guadalupe River. It is presumed
extirpated from the entire San Antonio
River system, as well as the Blanco
River and Johnson Creek.
In the mainstem Guadalupe River,
Texas fatmucket historically occurred in
Kerr County (OSUM 2011a, p. 1). In
1992 and 1995, surveys yielded no
evidence of the species (Howells 1994,
pp. 7–8; Howells 1996, p. 25), although
shell fragments collected in 1993 in
Guadalupe County may have been Texas
fatmucket but were too weathered for an
accurate determination (Howells 1995,
p. 31). In 1996, two live individuals
were recorded in Kerr County directly
below a dam (Howells 1997a, p. 36), and
in 1997, three shells were found at the
same site following a flood (Howells
1998, p. 18). No Texas fatmucket or
other freshwater mussels have been
found at that site since, and it is
unlikely that Texas fatmucket persist
there (Howells 2006, p. 71). However,
20 recently dead individuals were
discovered approximately 1 km (0.6 mi)
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downstream in Louise Hayes Park
during a drawdown (Howells 1999, pp.
18–19), and 6 live individuals were
found at the same location in 2005
(Howells 2006, pp. 71–72). Surveys in
2007 and 2008 yielded no live or
recently dead individuals (Burlakova
and Karatayev 2010a, p. 12). It is likely
that the species persists in the vicinity.
There has been no other evidence of
Texas fatmucket in the mainstem
Guadalupe River in recent years.
In 1999, two recently dead Texas
fatmucket were found in North Fork
Guadalupe River (Howells 2000a, p. 27).
This river was surveyed again in 2000
and 2003 at several sites, and no Texas
fatmucket were found (Howells 2001, p.
31; Howells 2004, pp. 13–14).
Johnson Creek was a historical
location for Texas fatmucket, but no live
freshwater mussels of any species have
been found in this stream for decades
(Howells 1996, p. 25; Howells 1998, p.
18; Howells 2002a, p. 8). Additionally,
the Blanco River has been surveyed
extensively since 1992, and no evidence
of Texas fatmucket has been collected,
nor is suitable habitat present (Howells
1994, p. 9; Howells 1995, pp. 32–33;
Howells 1996, p. 28; Johnson 2011, p.
1). The last collection of Texas
fatmucket from the Blanco River
occurred in the 1970s or 1980s (Howells
2005, p. 10).
Texas fatmucket have also been
extirpated from the entire San Antonio
River system. The mainstem San
Antonio River was surveyed in 1993
and 1996, and no live or dead Texas
fatmucket were found (Howells 1995, p.
35; 1997a, pp. 41–42). It was known
from the Medina River, a tributary to the
San Antonio River, historically
(Randklev et al. 2010c, p. 3), but no
mussels of any species have been found
in this river in recent years (May 2011,
pers. comm.). Additionally, although
Texas fatmucket were collected from
Cibolo Creek historically (OSUM 2011a,
p. 1) and shell material, likely from
Texas fatmucket, was found in 1993
(Howells 1995, p. 36), no live freshwater
mussels have been found in Cibolo
Creek since (Howells 1997a, pp. 40–41).
Summary
Based on historical and current data,
the Texas fatmucket has declined
significantly rangewide and has been
extirpated from most of the Guadalupe
River system and hundreds of miles of
the Colorado River, as well as from
numerous tributaries. Extant
populations are represented by only a
few individuals, and they are highly
disjunct and restricted to short reaches.
Two of the populations considered
extant in recent years may now be
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extirpated, and the remaining seven
populations are extremely small and
likely not stable. No evidence of recent
recruitment has been found in any of
the populations, with the possible
exception of the Llano River.
Species Information for Golden Orb
Species Description
The golden orb is small, usually less
than 82 mm (3.2 in), with an oval to
nearly round, smooth, and unsculptured
shell, except for concentric growth rings
(Howells 2002b, p. 6). External shell
coloration varies from yellow-brown,
gold, or orangish-brown to dark brown
or black, and some individuals may
show faint greenish rays. Internally, the
nacre is white to bluish-white (Howells
2002b, p. 6).
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Taxonomy
The golden orb was originally
described as Unio aureas by Lea in 1859
and later moved to the genus Quadrula
in 1900 (Simpson 1900, p. 783). Graf
and Cummings (2007, p. 18) have
proposed moving it to the genus
Amphinaias, but other freshwater
mussel taxonomists recommend waiting
for additional work to be completed on
members of Quadrula before splitting
the genus (Bogan 2011, pers. comm.).
Because the golden orb can exhibit an
elongated shell structure in headwater
riffles, old records of Unio bolli in the
Colorado River (Dall 1882, p. 956) are
very likely elongated forms of golden
orb (Howells 2010a, p. 5). The golden
orb is recognized by the Committee on
Scientific and Vernacular Names of
Mollusks of the Council of Systematic
Malacologists, American Malacological
Union (Turgeon et al. 1998, p 36), and
we recognize it as a valid species.
Biology and Life History
There is no specific information on
age, size of maturity, or host fish use for
golden orb. Other species in the genus
Quadrula successfully parasitize catfish,
and it is likely golden orb do as well
(Howells 2010a, p. 3). Gravid females
have been found from May through
August (Howells 2000b, p. 38). Mussels
in the genus Quadrula are short-term
brooders, which are species that hold
fertilized eggs and glochidia for a short
period, usually 3 to 6 weeks, before
releasing glochidia (Gorden and Layzer
1989, p. 6; Garner et al. 1999, p. 277).
Habitat
The golden orb has been found almost
exclusively in flowing waters in
moderately sized rivers (Howells 2010a,
p. 3). It has been found in only one
reservoir in the lower Nueces River
(Lake Corpus Christi), where wave
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action may simulate flowing water
conditions (Howells 2010a, p. 3). This
species is found in substrates of firm
mud, sand, and gravel, and it does not
appear to tolerate more unstable
substrates such as loose sand or silt
(Howells 2002b, p. 6).
Distribution and Abundance
Historical Distribution
The golden orb is endemic (native) to
nearly the entire lengths of the
Guadalupe, San Antonio, and NuecesFrio River basins in central Texas
(Howells 2010a, p. 5), including the
Guadalupe, Medina, San Antonio, Frio,
and Nueces Rivers and Cibolo Creek. It
was originally reported from four sites
in the Brazos River system (Strecker
1931, p. 63), but these are almost
certainly misidentified smooth
pimpleback (Howells 2002b, p. 5) based
on numerous mussel surveys
throughout the Brazos River system
since the 1970s that failed to find any
golden orb. The species has not been
found in studies of archaeological
specimens from the Brazos River
(Howells 2010a, p. 5), further indicating
golden orb did not historically occur in
the Brazos River system.
The golden orb has also been reported
from the upper Colorado River drainage
(Howells et al. 1996, pp. 108–109;
Randklev et al. 2010c, p. 4), but these
appear to have been misidentified Texas
pimpleback (Howells 2010a, p. 5). Since
no other golden orb have been reported
from the Colorado River system, we do
not believe it occurred in that basin.
Current Distribution
Based on historical and current data,
the golden orb has declined
significantly rangewide and is now
known from only four streams in
disjunct locations. Despite mussel
surveys across the historical range, since
1995 golden orb has only been found in
Lake Corpus Christi and the Guadalupe,
lower San Marcos, and lower San
Antonio Rivers. The species has been
extirpated from the entire Nueces-Frio
River basin, except at the extreme
downstream end of the Nueces River,
where a population persists in Lake
Corpus Christi. Aside from the upper
Guadalupe River, all existing
populations occur in the lower portion
of occupied basins in a small
geographical area; only about 130 km
(80 mi) separate the farthest two
populations. Only four populations
appear to be relatively stable and
recruiting, while the remaining five
populations are represented by only a
few individuals.
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Guadalupe River System
In the Guadalupe River system, the
golden orb historically ranged
throughout the length of the Guadalupe,
San Antonio, and San Marcos Rivers.
Currently in this basin, the species only
persists in the uppermost Guadalupe
River and lower San Marcos, San
Antonio, and Guadalupe Rivers. The
lower portion of this basin (within
approximately 120 km (75 mi) of the
Gulf of Mexico) harbors all four of the
large, presumably reproducing
populations of golden orb.
Historically known from the
mainstem Guadalupe River (Howells
2002a, p. 8), the golden orb was not seen
in the upper Guadalupe River in Kerr
County again, despite repeated surveys
(Howells 1994, pp. 7–8; 1996, p. 30;
1997a, p. 36), until 1997, when three
shells were discovered (Howells 1998,
p. 18). No live freshwater mussels of any
species have been found in this area,
just downstream of a dam, since 1997
(Howells 1999, p. 18; Howells 2006, p.
71), and it is unlikely golden orb
persists there. However, upstream of
this area, above the dam and
impounded reach, a single recently dead
individual was found in 1998 during an
extended drawdown of the river to
construct a footbridge in a local park
(Howells 1999, pp. 18–19). In 2005, two
live individuals were also found at this
site (Howells 2006, pp. 71–72), showing
that the species had survived the
drawdown and persists at the site.
Golden orb also occurs farther
downstream in the mainstem Guadalupe
River, near Lake Gonzales in Gonzales
County. Upstream of the reservoir,
subfossil shells (very old shells that are
brittle, crumbling, and with extensive
erosion) were found in 1993 (Howells
1995, p. 31), but the species has not
been found there since. However, below
the reservoir, one recently dead
individual was collected in 1995
(Howells 1996, pp. 26–27), and in 1996,
25 live golden orb were recorded at two
sites in this area (Howells 1997a, pp.
37–38). Later, in 2006, three live golden
orb were also found in this area
(Howells 2006, pp. 85–86). A small
population apparently continues to
persist below Lake Gonzales.
A large golden orb population occurs
farther downstream in the mainstem
Guadalupe River, below Lake Wood,
also in Gonzales County. Although none
were found during a survey in 1995
(Howells 1996, p. 27), 36 live golden orb
were found at two sites below Lake
Wood in 1996 (Howells 1997a, pp. 38–
40). Density estimates were calculated
based on the quantitative information
collected from these surveys, but they
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were not considered statistically valid
(Howells 1997a, p. 40) and so are not
reported here. Only one live golden orb
was found at this site in 2002 (Howells
2003, p. 11), but a relatively large
population continues to persist; a total
of around 100 live golden orb were
found at three sites within 2 km (1.2 mi)
of the Lake Wood Dam in 2006 (Howells
1996, pp. 87–91). Also, in 2008, 33
golden orb were recorded alive
downstream of Lake Wood (Burlakova
and Karatayev 2010a, p. 14). This
portion of the Guadalupe River supports
a relatively large population of golden
orb, and it also contains one of the most
abundant freshwater mussel
communities in Texas (Burlakova and
Karatayev 2010a, p. 14).
In 2009, a large population of golden
orb was discovered farther downstream
in the mainstem Guadalupe River in
Victoria County, when over 100
individuals were found (Johnson 2009,
p. 1). Multiple size classes were
observed, including juveniles,
indicating this population is
reproducing and recruiting new
individuals into the population. A large
number of shells was collected
upstream of this site in 1994 (Burlakova
and Karatayev 2010c, p.1), but no
golden orb were seen alive until 2009.
The San Marcos River, a tributary to
the Guadalupe River, also supports a
large golden orb population near its
confluence with the tailwaters (outflow)
of Lake Wood Dam. Although much of
the San Marcos River has been
extensively surveyed, with very few
freshwater mussels present of any
species (Howells 1995, pp. 33–34;
1997a, p. 40; 2004, pp. 15–16, 18; 2005,
p. 10), one old golden orb shell was
found near the town of Staples (Howells
1998, p. 19), and a single live individual
was found near the town of Luling
(Howells 1999, p. 28). Downstream from
these locations, a large population
persists in the vicinity of Palmetto State
Park in Gonzales County. In 1995, a
recently dead individual was discovered
downstream of the park, indicating the
recent presence of the species (Howells
1996, p. 28), and, based on surveys from
2000–2006, a relatively large population
was confirmed to be in the area
(Howells 2001, pp. 32–33; 2006, pp. 72–
73; 2006, p. 91; Burlakova and
Karatayev 2010a, pp. 14–15).
Historically, golden orb were
numerous in the San Antonio River in
Karnes County (OSUM 2011b, p. 1), but
only a single subfossil shell was found
at each of two sites in Karnes County in
1996 (Howells 1997a, pp. 41–42). No
live animals have been found there
since, although abundant shell material
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remains present (Karatayev and
Burlakova 2008, p. 40).
The lower portion of the San Antonio
River supports the largest known golden
orb population. In 2007, 37 live golden
orb were recorded near Goliad in Goliad
County, both within and downstream of
Goliad State Park (Howells 2009, p. 11).
The following year, 285 live golden orb
were found within the park and
downstream surrounded by private
lands (Burlakova and Karatayev 2010a,
p. 15). This site represents the largest
known population of golden orb.
In 2009, a single live golden orb was
discovered in the lower San Antonio
River south-southwest of Victoria in
Victoria County (Johnson 2009, p. 1);
this site has not been surveyed since.
We presume golden orb may persist in
this stretch of river.
The golden orb appears to have been
extirpated from the Medina River. The
species historically occurred in Medina
and Bexar Counties (Randklev et al.
2010b, p. 4; OSUM 2011b, p. 1), but no
live or dead mussels of any species have
been found in this river in recent years
(May 2011, pers. comm.).
Cibolo Creek, a tributary to the San
Antonio River, was extensively
surveyed in the 1990s, with only old
golden orb shells collected in Wilson
County (Howells 1995, pp. 35–37;
1997a, pp. 40–41). In 2006 and 2007,
Burlakova and Karatayev (2010b, p. 1)
surveyed this same general area and
found only shell material. It is unlikely
golden orb remain in Cibolo Creek.
Nueces-Frio River System
Information is limited on the
occurrence of golden orb in the Nueces
River. Other than a population that
occurs in a reservoir on the lower
Nueces River (Lake Corpus Christi), the
species appears to be extirpated from
the remainder of the basin.
Historically, the golden orb occurred
in the Nueces River in Live Oak County
(OSUM 2011b, p. 1). It was last seen
alive in the Nueces River in 1993, when
unreported numbers were found in the
same area (Burlakova and Karatayev
2010c, p. 1). A shell was collected in the
same general area in 1995 (Burlakova
and Karatayev 2010c, p. 1), but
additional surveys in 1996 and 1997
found no evidence of the species
(Howells 1997a, pp. 43–44; 1998, p. 20).
We presume the species no longer
occurs in the upper portions of the
Nueces River.
An anomalous (odd) population of
golden orb has persisted in Lake Corpus
Christi Reservoir in the lower Nueces
River. While the species does not
typically inhabit lentic (ponded) water,
wave action is presumed to simulate
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flowing water conditions and has
supported a golden orb population since
at least the 1970s (OSUM 2011b, p. 1).
A few live individuals of golden orb
have been found within the reservoir
consistently since 1994 (Howells 1995,
p. 39; 1996, pp. 30–31; Burlakova and
Karatayev 2010c, p. 1). Numbers of
golden orb collected increased in 1996,
when 86 live golden orb were found at
three different locations within the
reservoir (Howells 1996, pp. 30–31).
However, a drawdown of the lake in
1996 resulted in large numbers of
golden orb stranded and killed (Howells
2010a, p. 9), and in 1998 no live
individuals were found (Howells 1999,
p. 19). Again in 2005, no live
individuals were found during surveys,
but in 2006, a total of nine were
collected at three different sites within
the reservoir (Howells 2006, pp. 73–76,
91–93). A small golden orb population
likely persists in the reservoir.
Very little information is available on
the distribution of golden orb in the Frio
River. Shells were last seen in
McMullen County in 1994 (Burlakova
and Karatayev 2010c, p. 1), but no
evidence of the species has been found
in this river since (Howells 1995, pp.
37–38; 1996, p. 29; 2002a, pp. 9–10;
2004, pp. 19–20).
Summary
Based on historical and current data,
the golden orb has declined rangewide
and is now known from only nine
populations in four rivers and has been
eliminated from nearly the entire
Nueces-Frio River system. Four of these
populations appear to be stable and
reproducing; the remaining five
populations are small and isolated and
show no evidence of recruitment. Only
the populations in the middle
Guadalupe River and lower San Marcos
River are likely connected; the
remaining extant populations are highly
fragmented and restricted to short
reaches.
Species Information for Smooth
Pimpleback
Species Description
The smooth pimpleback is a nearly
round, thick-shelled freshwater mussel
that generally reaches at least 60 mm
(2.6 in) in length (Howells 2010b, p. 4).
It is moderately thick, solid, and
inflated. Externally, the smooth
pimpleback, like its name suggests, is
relatively smooth with minute
sculpturing; it may or may not have a
few small pustules (raised bumps)
(Howells 2010b, p. 2). The external
coloration of the shell ranges from tan
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to light brown, dark brown, and black
with no rays (Howells 2010b, p. 4).
Taxonomy
The smooth pimpleback was
originally described by Lea in 1859 as
Unio houstonensis. It was later placed
in the genus Margaron and ultimately
moved to Quadrula by Simpson (1900,
p. 782). Graf and Cummings (2007, p.
18) have proposed moving it to the
genus Amphinaias, but other freshwater
mussel taxonomists recommend waiting
for additional work to be completed on
members of Quadrula before splitting
the genus (Bogan 2011, pers. comm.).
The smooth pimpleback is recognized
by the Committee on Scientific and
Vernacular Names of Mollusks of the
Council of Systematic Malacologists,
American Malacological Union
(Turgeon et al. 1998, p 37), and we
recognize it as a valid species.
Biology and Life History
There is no specific information on
age, size of maturity, or host fish use for
smooth pimpleback. Numerous
individuals were examined for gravidity
between June and November, with no
evidence of eggs or glochidia (Howells
2000b, p. 38). Other species in the genus
Quadrula successfully parasitize catfish,
and it is likely smooth pimpleback does
as well (Howells 2010b, p. 2);
additionally, mussels in the genus
Quadrula are typically short-term
brooders (Gorden and Layzer 1989, p. 6;
Garner et al. 1999, p. 277), and we
expect the same of the smooth
pimpleback.
Habitat
The smooth pimpleback has been
found in mud, sand, and fine gravel in
medium-to-large rivers and some
reservoirs (Howells 2010b, p. 3). Unlike
most other Quadrula species in central
Texas, smooth pimpleback do occur in
some reservoirs (Howells 2002b, p. 8;
2010b, p. 3).
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Distribution and Abundance
Historical Distribution
The smooth pimpleback is native to
the central and lower Brazos and
Colorado Rivers and their tributaries in
central Texas (Howells 2010b, p. 4). The
smooth pimpleback has also been
reported from the Trinity River and
other drainages in Texas, as well as from
areas outside of Texas, including
southern Arkansas and the Verdigris
River in Kansas. These reports are likely
misidentifications of other pimpleback
species that can sometimes closely
resemble smooth pimpleback (Howells
2010b, pp. 4–5). The smooth
pimpleback was historically uncommon
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where it occurred; from the 1960s
through the 1990s, experts failed to find
large populations persisting throughout
its range (Howells 2009, p. 12).
In the Colorado River, historical
reports indicate that the smooth
pimpleback occurred from San Saba
County downstream to Wharton County,
as well as in the Llano River and Onion
and Skull Creeks. Within the Brazos
River basin, the species historically
occurred throughout the length of the
mainstem of the Brazos River (Howells
2009, p. 12), as well as in the Clear Fork
Brazos, Leon, Navasota, Little Brazos,
San Gabriel, Lampasas, and Little Rivers
and Yegua Creek (Howells 2010b, pp. 4–
6; Randklev et al. 2010b, p. 20).
Current Distribution
The smooth pimpleback has been
nearly extirpated from the Colorado
River basin, and a few small
populations persist in the Brazos River
basin. Recent surveys suggest a greater
abundance and distribution of the
smooth pimpleback in the central
Brazos River drainage than was
indicated by collections from the past
40 years, with five populations
represented by more than a few
individuals.
Colorado River System
The smooth pimpleback historically
occurred throughout the mainstem
Colorado River as well as several
tributaries, but it is currently restricted
to one mainstem reservoir, two sites on
the mainstem Colorado River, and the
San Saba River. Populations in all of the
other historically occupied tributaries
and two reservoirs appear to have been
extirpated.
In the mainstem Colorado River,
smooth pimpleback were historically
known from much of the length of the
river (Howells 1996, p. 21; 1997a, pp.
34–35; Randklev et al. 2010c, p. 4;
OSUM 2011c, p. 1). Numerous surveys
in many locations on the Colorado River
occurred between 1993 and 2009, and
no evidence of smooth pimpleback was
found (Howells 1995, p. 29; 1996, p. 23;
1997a, pp. 27, 31; 2002a, p. 6; 2004, p.
7, 11; 2005, p. 6; Burlakova and
Karatayev 2010a, pp. 15–16), except for
in Colorado County in 1999, when three
live smooth pimpleback were found
(Howells 2000a, p. 27). During two
surveys in 2009, live smooth
pimpleback were found in the same
general area as in 1999 (Burlakova and
Karatayev 2010a, p. 16; Johnson 2009, p.
1). Farther downstream, in Wharton
County, live smooth pimpleback were
found at two sites in 2009 (Burlakova
and Karatayev 2010a, p. 16), despite
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having been surveyed in 1995 and none
found (Howells 1996, p. 23).
Inks Lake is a small mainstem
reservoir on the Colorado River in
Burnet County. Several live smooth
pimpleback were found in 1992
(Howells 1994, p. 4); however, since
that time only shell material has been
found during four separate surveys
between 1996 and 2005 (Howells 1997a,
pp. 32–33; 1999, p. 16; 2005, p. 8; 2006,
p. 67). Frequent drawdowns in this lake
appear to have affected all species of
freshwater mussels, as there has been a
sharp decline in the overall mussel
community (Howells 1999, p. 16).
One live smooth pimpleback was
found in Lake Lyndon B. Johnson, a
large mainstem reservoir on the
Colorado River, in 2001, but no live
individuals have been found since
(Howells 2002a, pp. 6–7; 2006, pp. 68–
69). Farther downstream, in Lake
Marble Falls, 13 live smooth
pimpleback were found in 1995 during
a drawdown of lake levels (Howells
1996, p. 22), but subsequent surveys in
1996 failed to find any additional living
animals (Howells 1997a, p. 33). The
small recent survey effort is not
sufficient to conclude that the smooth
pimpleback no longer occur in these
lakes, and small populations may still
persist there.
Smooth pimpleback were recently
found in the San Saba River in San Saba
County, when 29 individuals were
found at two locations (Burlakova and
Karatayev 2011, p. 5). Various size and
age classes were represented, indicating
a reproducing, recruiting population
(Burlakova and Karatayev 2011, p. 5).
Even more recently, 206 smooth
pimpleback, including adults and
juveniles, were recorded in this same
area in riffle and pool habitat (Randklev
2011b, p. 1).
No smooth pimpleback populations
remain in any of the Colorado River
tributaries in which the species was
historically known to occur, including
the full length of the Llano River
(Howells 1996, pp. 21–22; 1998, p. 17;
2000a, p. 25; 2005, p. 8; Randklev et al.
2010c, p. 4; OSUM 2011c, p. 1). A single
subfossil shell, likely a smooth
pimpleback, was found in the Llano
River in Kimble County in 1995
(Howells 1996, pp. 21–22), but no other
evidence of the species has been found
in the Llano River in recent years.
Additionally, although Onion and Skull
Creeks were historically occupied by
smooth pimpleback (Randklev et al.
2010c, p. 4), the species has not been
found recently in either stream (Howells
1995, pp. 28–29).
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Brazos River System
The smooth pimpleback historically
occurred in the Brazos River system
from Palo Pinto County downstream to
Austin and Waller Counties, as well as
in numerous tributaries. The species has
been extirpated from the upstream half
of the mainstem Brazos River and from
at least three tributaries. Substantial
populations persist in the Leon River,
Navasota River, and Yegua Creek, and
small populations remain in the lower
Brazos and Little Brazos Rivers.
In the mainstem Brazos River, surveys
in Palo Pinto, Somervell, and Bosque
Counties between 1996 and 2000
indicate that the smooth pimpleback has
been extirpated from the upstream
portion of the river (Howells 1997a, pp.
16, 18–19; 1999, pp. 11–12; 2001, p. 19).
Despite surveys in 1996 and 1998 in
which no individuals were found
(Howells 1997a, p. 21; 1999, p. 12), a
single live smooth pimpleback was
found in McLennan County in the
middle Brazos River in 2005 (Howells
2010b, p. 5), and two live individuals
were recorded in Falls County in 2006
(Karatayev and Burlakova 2008, pp. 6–
10).
Although not extirpated from the
middle Brazos River, the smooth
pimpleback occurs only in low
numbers. In Milam and Robertson
Counties, no smooth pimpleback were
found in 1998 (Howells 1999, p. 13), but
eight live individuals were found in
2006 (Burlakova and Karatayev 2010b,
p. 1). More recently, in 2008, 13 live
smooth pimpleback were found at the
same site (Randklev et al. 2009, p. 18).
Additionally, downstream in Burleson
and Brazos Counties, which were
historically occupied by the smooth
pimpleback (OSUM 2011c, p. 1), a small
population persists. In 1995, one live
and one recently dead individual were
collected within Brazos County
(Howells 1996, pp. 17–18). Although
none were found here in 1999 (Howells
2000a, pp. 21–22), in 2006 a single live
smooth pimpleback was collected at this
site (Karatayev and Burlakova 2008, pp.
6–10). Additionally, further downstream
in Grimes and Waller Counties, a single
live individual was found in 2006
(Burlakova and Karatayev 2010b, p. 1)
and again in 2008 (Randklev et al. 2009,
p. 18). Smooth pimpleback are more
numerous in the lower mainstem Brazos
River, in Austin and Waller Counties,
where 38 live individuals were found in
2006 (Karatayev and Burlakova 2008,
pp. 6–10).
Tributaries to the Brazos River also
contain smooth pimpleback
populations. The Leon River, in the
Little River drainage of the Brazos,
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historically contained smooth
pimpleback throughout its length in
Hamilton, Coryell, and Bell Counties
(Howells 1994, p. 19, 1997a, p. 20;
Randklev et al. 2010c, p. 4; OSUM
2011c, p. 1). Currently, a smooth
pimpleback population persists in
Hamilton County, where numerous live
individuals were found in 2006 and
2011 (Howells 2006, pp. 82–83;
Randklev 2011a, p. 1), as well as several
locations in Coryell County, where
numerous individuals were also
recently found (Randklev 2011a, p. 1).
Only subfossil smooth pimpleback
shells have been found in the Lampasas
River in Bell County in 1996 (Howells
1997a, pp. 20, 23). Subsequent surveys
of the river in both Bell and Lampasas
Counties yielded no evidence of smooth
pimpleback (Howells 1999, p.14; 2001,
p. 20), and the species has likely been
extirpated from the Lampasas River.
The Little River in Milam County is
also a historical location for the smooth
pimpleback (Randklev et al. 2010c, p.
4). Old shells were found at this site in
1996 (Howells 1997a, p. 22), and a
single live individual was found here in
2006 (Karatayev and Burlakova 2008, p.
6). Farther downstream, at the
confluence with the Brazos River, none
have been found (Howells 1996, p. 17).
A single old smooth pimpleback shell
has been found in the San Gabriel River
in Milam County (Howells 1997a, p. 23),
and it is likely the species has been
extirpated from this Brazos River
tributary as well.
In the Little Brazos River, the smooth
pimpleback appears to persist in low
numbers. Although none were found in
Robertson County in 1993 and there had
appeared to be a die off of numerous
freshwater mussel species (Howells
1995, p. 18), one live smooth
pimpleback was found during a 2006
survey (Karatayev and Burlakova 2008,
p. 6). Farther downstream in Brazos
County, recently dead individuals were
discovered in 2001 (Howells 2002a, pp.
4–5). The species occurred in this area
historically (Randklev et al. 2010c, p. 4),
and reports of mussels in the Little
Brazos River from the 1950s described
the freshwater mussel community as
numerous, including smooth
pimpleback (Gentner and Hopkins 1966,
pp. 458–459), but no live individuals
have been collected in this area in
recent years (Howells 1996, p. 18; 1999,
p. 14).
The smooth pimpleback has been
extirpated from the Clear Fork Brazos
River. Although this species was
originally documented from this river in
Shackelford County in 1893 (Randklev
et al. 2010c, p. 4), none have been found
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in this stream since (Howells 1999, p.
19).
In the Navasota River, smooth
pimpleback historically occurred in
Leon, Brazos, Grimes, and Washington
Counties (Randklev et al. 2010c, p. 4;
OSUM 2011c, p. 1). Currently, the
species persists in each of those
counties, with a large population
occurring in the lower river. In Leon
County three recently dead smooth
pimpleback shells were found in 2000
(Howells 2001, p. 23), indicating that a
few individuals may persist in the area.
However, one of the largest known
populations occurs farther downstream
near the confluence of the Navasota and
Brazos Rivers. Nine live individuals
were found in this area in 2006
(Karatayev and Burlakova 2008, pp. 6–
10), and in 2008 a total of 117 live
smooth pimpleback were recorded at 3
different locations within Washington
and Grimes Counties (Randklev et al.
2009, pp. 6, 18). A large population
continues to persist in the Navasota
River, with a total of 314 smooth
pimpleback recorded at two sites in
2011 (Randklev 2011a, p. 1).
In Yegua Creek, no smooth
pimpleback were found during several
surveys between 1996 and 2003
(Howells 1997a, pp. 24–26; 2001, p. 22;
2004, p. 6), although subfossil shells
were found in Washington County in
1996. However, in 2006, a live
individual was discovered (Karatayev
and Burlakova 2008, pp. 6–10), which
prompted further surveys in 2008.
Numerous smooth pimpleback were
found during subsequent surveys at four
different locations within Washington
and Burleson Counties (Randklev et al.
2009, pp. 16–18; Randklev 2011a, p. 1),
indicating the presence of a potentially
large population in this stream.
Summary
Based on historical and current data,
the smooth pimpleback has declined
rangewide and is now known from only
nine locations. The species has been
eliminated from nearly the entire
Colorado River and all but one of its
tributaries, as well as from the upper
Brazos River and several tributaries. The
San Saba River, lower Brazos River,
Navasota River, Leon River, and Yegua
Creek populations appear to be stable
and reproducing, but the remaining
populations are small, isolated, and
represented by only a few individuals.
Species Information for Texas
Pimpleback
Species Description
The Texas pimpleback is a large
pimpleback species with a moderately
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inflated shell that generally reaches 60–
90 mm (2.4–3.5 in) (Howells 2002b, pp.
3–4). With the exception of growth
lines, the shell of the Texas pimpleback
is generally smooth and moderately
thick (Howells 2002b, p. 4). Externally,
coloration ranges from yellowish-tan to
dark brown with some individuals
mottled or with dark green rays.
Internally, the nacre is white and
iridescent posteriorly (Howells 2002b,
p. 4).
Taxonomy
The Texas pimpleback was originally
described as Unio petrinus by Gould in
1855. It was placed in the genus
Margaron by Lea in 1870 and ultimately
moved to Quadrula by Simpson in 1900
(Simpson 1900, p. 783). Graf and
Cummings (2007, p. 18) have proposed
moving it to the genus Amphinaias, but
other freshwater mussel taxonomists
recommend waiting for additional work
to be completed on members of
Quadrula before splitting the genus
(Bogan 2011, pers. comm.). The Texas
pimpleback is recognized by the
Committee on Scientific and Vernacular
Names of Mollusks of the Council of
Systematic Malacologists, American
Malacological Union (Turgeon et al.
1998, p. 37), and we recognize it as a
valid species.
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Biology and Life History
There is very little specific
information on age, size of maturity, or
host fish use for Texas pimpleback.
Gravid females have been found from
June through August, and the smallest
documented gravid female was 45 mm
(1.8 in) long (Howells 2000b, p. 38).
Glochidia are hookless and elliptical in
shape (Howells et al. 1996, p. 120). To
date, no host fish have been confirmed
for the Texas pimpleback; however,
glochidia have been reported attached to
and encysted on flathead catfish
(Pylodictis olivaris), yellow bullhead
(Ameiurus natalis), and bluegill in
laboratory settings, although none
transformed to the juvenile stage
(Howells 2010e, p. 3). This is consistent
with other species in the genus
Quadrula, which also parasitize catfish
species.
Habitat
The Texas pimpleback typically
occurs in moderately sized rivers,
usually in mud, sand, gravel, and
cobble, and occasionally in gravel-filled
cracks in bedrock slab bottoms (Horne
and McIntosh 1979, p. 122; Howells
2002b, p. 4). The species has not been
found in water depths over 2 m (6.6 ft).
Texas pimpleback have not been found
in reservoirs, which indicates that this
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species is intolerant of deep, lowvelocity waters created by artificial
impoundments (Howells 2002b, p. 4). In
fact, Texas pimpleback appear to
tolerate faster water more than many
other mussel species (Horne and
McIntosh 1979, p. 123).
Distribution and Abundance
Historical Distribution
The Texas pimpleback is endemic to
the Colorado and Guadalupe-San
Antonio River basins of central Texas
(Howells 2002b, p. 3). In the Colorado
River basin, Texas pimpleback occurred
throughout nearly the entire mainstem,
as well as numerous tributaries,
including the Concho, North Concho,
San Saba, Llano, and Pedernales Rivers,
and Elm and Onion Creeks (Howells
2010e, p. 5; Randklev et al. 2010c, p. 4;
OSUM 2011d, p. 1). Within the
Guadalupe-San Antonio River basin, it
occurred throughout most of the length
of the Guadalupe River, as well as in the
San Antonio, San Marcos, Blanco, and
Medina Rivers (Horne and McIntosh
1979, p. 122; Howells 2010e, p. 5;
OSUM 2011d, p. 1).
Current Distribution
The Texas pimpleback has declined
significantly rangewide, and only four
streams—the San Saba River, Concho
River, Guadalupe River, and San Marcos
River—are known to harbor persisting
Texas pimpleback populations. These
populations are disjunct, small, and
isolated. The species has been
extirpated from the remainder of its
historical range.
Colorado River System
In the Colorado River system, Texas
pimpleback once occurred throughout
the mainstem and in many major
tributaries. Currently, the species has
been extirpated from the Pedernales,
North Concho, and Llano Rivers, as well
as Onion Creek. It has also likely been
extirpated from the mainstem Colorado
River and Elm Creek. The Concho River
contains the most abundant population
of Texas pimpleback and one of only
two populations of the species likely to
be remaining in the Colorado River
system, but most individuals are old
and there has been very little evidence
of recruitment.
In the mainstem Colorado River,
Texas pimpleback historically occurred
from Runnels County downstream to
Colorado County (Howells 2010e, p. 5;
Randklev et al. 2010c, pp. 3–4; OSUM
2011d, p. 1). However, surveys in
numerous locations along the river
yielded no evidence of the species
anywhere except in Runnels and San
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Saba Counties (Howells 1995, pp. 20,
29; 1997a, pp. 27, 31, 35; 2000a, p. 27;
2002a, p. 7). In Runnels County, Texas
pimpleback shells were found in 1993
(Howells 1995, p. 20), but several
subsequent surveys between 1996 and
2008 detected no further evidence of the
species (Howells 1997a, p. 27; 1998, p.
10; 2002a, p. 7; 2004, p. 7; Burlakova
and Karatayev 2010a, p. 10). In San Saba
County, a single shell was collected in
1989 (Howells 2002b, p. 6), and three
recently dead individuals were found in
1999 (Howells 2000a, pp. 25–26). An
additional shell was collected in 2001
(Howells 2002a, p. 6). No live
individuals have been collected from
this reach of the Colorado River.
In Runnels County, Elm Creek once
supported a Texas pimpleback
population. Small numbers of Texas
pimpleback were found in 1993 and
1995 (Howells 1995, p. 21; 1996, p. 20),
but none were found in 1997, 2001, or
2003 (Howells 1998, p. 11; 2002a, p. 5;
2004, p. 7). In 2005 and 2008, only dead
individuals were collected (Howells
2006, pp. 63–64; Burlakova and
Karatayev 2010a, p. 10). No live
individuals have been found in over a
decade despite repeated sampling
efforts, and it is likely the Texas
pimpleback has been extirpated from
this stream.
The Concho River in Concho County
supports the largest Texas pimpleback
population. Thirteen and 28 individuals
were collected in 1993 and 1994,
respectively (Howells 1995, pp. 24–25;
2006, p. 61). However, low water and
high temperatures in 1997 killed large
numbers of many freshwater mussel
species in the area up and downstream
of Paint Rock, and 63 recently dead
Texas pimpleback were found (Howells
1998, pp. 14–15). A severe drought in
1999 resulted in this area of the Concho
River being reduced to a series of small
pools. Few live Texas pimpleback were
collected during this drought, in
addition to many recently dead
individuals (Howells 2000a, p. 23). No
evidence of the species was found in
2004 (Howells 2005, p. 9), but eight live
individuals were found in 2005
(Howells 2006, p. 60), evidence that the
species had survived the extreme
dewatering of the river. In 2008, 61 live
Texas pimpleback were collected in this
same area, and the population was
estimated to contain approximately
4,000 individuals (Burlakova and
Karatayev 2010a, p. 10; 2010b, p. 1).
However, the average length of
individuals collected at this site was
over 90 mm (3.5 in), indicating that
reproduction is limited in this
population. Further, although no mussel
surveys occurred in 2009 and 2010, the
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river was reported to be extremely low
during this time (Howells 2010e, p. 6);
the result of this additional dewatering
on the population is unknown.
The San Saba River historically
contained Texas pimpleback (Randklev
et al. 2010c, p. 2), but no live
individuals had been collected in over
a decade until recently when shells
were collected in 1992 and 1995
(Howells 1994, p. 7; 1996, p. 21), and
five live individuals were collected in
1997 (Howells 1998, p. 16). However,
subsequent surveys were conducted in
2000, 2004, and 2005, with only shell
material being found in 2000 (Howells
2001, pp. 28–29), and no evidence of
Texas pimpleback was found in 2004
and 2005 (Howells 2005, pp. 8–9; 2006,
pp. 64–65). A single shell was collected
in 2008 (Burlakova and Karatayev
2010b, p. 1). However, in 2011, 39 live
individuals were found at two sites in
San Saba County (Burlakova and
Karatayev 2011, p. 3). The individuals
found were of various sizes and ages,
indicating a reproducing population
(Burlakova and Karatayev 2011, p. 4).
Further surveys at this site confirm a
large population in the area, with 140
individuals, including many juveniles,
found here (Randklev 2011b, p. 1).
The Texas pimpleback also
historically occurred in the North
Concho, Pedernales, and Llano Rivers,
as well as Onion Creek (Howells 2010e,
p.5; Randklev et al. 2010c, p. 4; OSUM
2011d, p. 1); all are tributaries within
the Colorado River system. In the North
Concho River, all freshwater mussels are
presumed extirpated from historically
occupied areas (Howells 1995, pp. 22–
23). The Pedernales River historically
harbored a Texas pimpleback
population (OSUM 2011d, p. 1), but
only old shells have been collected in
this river in recent years (Howells 1994,
p. 5). Since 1993, no evidence of Texas
pimpleback has been found (Howells
1995, pp. 27–28; 1999, p. 16), and the
species is presumed to be extirpated.
Additionally, repeated surveys in the
Llano River in Kimble and Mason
Counties consistently failed to collect
live Texas pimpleback, with shells
found only in Llano County in 1997
(Howells 1996, pp. 21–22; 1998, p. 17;
2005, p. 8). The Texas pimpleback is
likely extirpated from all of these
streams.
Guadalupe River System
In the Guadalupe River system, the
Texas pimpleback has been extirpated
from nearly the entire reach of the
mainstem Guadalupe, San Antonio, and
Blanco Rivers. Very small populations
remain only in the lower Guadalupe and
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San Marcos Rivers, represented by one
or two individuals in each.
In the mainstem Guadalupe River, the
Texas pimpleback was historically
known throughout the length of the
river, from as long ago as 1905
(Randklev et al. 2010c, p. 1; OSUM
2011d, p. 1). Numerous surveys between
1992 and 2005 have not yielded any
evidence of the species anywhere but in
Victoria County (Howells 1994, pp. 7–
9; 1995, pp. 30–32; 1996, pp. 25–27;
1997a, pp. 37–40; 1999, pp. 18–19;
2002a, p. 8; 2003, pp. 15, 17; 2006, pp.
71–72; Johnson 2009, p. 1), where two
live individuals were collected in 2009.
A small population may remain in the
lower Guadalupe River.
In the San Marcos River near the
confluence with the Blanco River in
Hays County, repeated surveys between
1992 and 2000 yielded no evidence of
Texas pimpleback (Howells 1994, pp. 9–
10; 1995, pp. 33–34; 1996, p. 27; 1997a,
p. 40; 2000a, p. 28; 2001, pp. 32–33).
However, in 2003 two shells were
collected (Howells 2004, p. 16), and in
2004, a single live individual was found
(Howells 2005, p. 10). The Texas
pimpleback likely persists in this river
in very low numbers.
The Texas pimpleback appears to be
extirpated from the San Antonio River,
with only shell fragments found near
the City of San Antonio in Bexar County
in 1993 (Howells 1995, p. 35). No
evidence of the species was found
downstream in Karnes County in 1996
(Howells 1997a, pp. 41–42).
The Texas pimpleback was once
described as abundant in the Blanco
River just upstream of its confluence
with the San Marcos River in Hays
County (Horne and Mcintosh 1979, p.
126), but repeated surveys of this area
between 1992 and 1995 yielded no
recent evidence of the species (Howells
1994, p. 9; 1995, pp. 32–33; 1996, p. 27),
with only a subfossil shell collected in
1993 (Howells 1995, p. 33). No shell
material or live individuals were found
in additional surveys in 2011 (Johnson
2011, p. 1).
Summary
The Texas pimpleback has been
eliminated from long reaches of former
habitat in hundreds of miles of the
Colorado and Guadalupe River systems.
Only two populations appear large
enough to be stable, but evidence of
recruitment in the Concho River
population is limited. The San Saba
River population may be the only
remaining recruiting population of
Texas pimpleback. Two additional
populations are represented by one or
two individuals; all populations are
highly disjunct.
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Species Information for Texas
Fawnsfoot
Species Description
The Texas fawnsfoot is a small,
relatively thin-shelled freshwater
mussel that can reach 60 mm (2.4 in) in
length but is usually much smaller
(Howells 2010d, p. 2). The shell is long
and oval, generally free of external
sculpturing, with external coloration
that varies from yellowish- or orangishtan, brown, reddish-brown, to smokygreen with a pattern of broken rays or
irregular blotches (Howells 2010d, p. 2).
The nacre is bluish-white or white and
iridescent posteriorly (Howells 2010d,
p. 2).
Taxonomy
The Texas fawnsfoot was first
described as Unio macrodon by Lea in
1859 and was subsequently placed in
the genus Margaron by Lea in 1870 and
then moved to Plagiola by Simpson
(1900, p. 605). Ultimately the species
was placed in the genus Truncilla by
Strecker (1931, pp. 63, 65). The Texas
fawnsfoot is recognized by the
Committee on Scientific and Vernacular
Names of Mollusks of the Council of
Systematic Malacologists, American
Malacological Union (Turgeon et al.
1998, p. 37), and we recognize it as a
valid species.
Biology and Life History
There is no specific information on
age, size of maturity, or host fish use for
Texas fawnsfoot. However, other species
in the genus Truncilla parasitize
freshwater drum (Aplodinotus
grunniens) (OSUM 2011f, p. 1), and it is
likely the Texas fawnsfoot does as well.
Freshwater drum are ubiquitous
throughout the range of Texas fawnsfoot
(Hubbs et al. 2008, p. 53).
Habitat
Since Texas fawnsfoot were not found
alive for many years, very little
information is available about its habitat
preferences. In the past only Texas
fawnsfoot shells and recently dead
individuals were occasionally found
along rivers following drought-related
dewatering or bank deposition after high
floods. These shells and recently dead
individuals indicated that the Texas
fawnsfoot occurs in flowing water, as it
was never found in ponds, lakes, or
reservoirs, suggesting that it is intolerant
of deep, low-velocity waters created by
artificial impoundments (Howells
2010d, p. 3). The recently discovered
live population in the Brazos River
indicates that the species occurs in
rivers with soft, sandy sediment with
moderate water flow (Randklev and
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Lundeen 2010, p. 1; Randklev et al.
2010a, p. 298; Johnson 2011, p. 1).
Distribution and Abundance
Historical Distribution
The Texas fawnsfoot is endemic to the
Brazos and Colorado Rivers of central
Texas (Howells et al. 1996, p. 143;
Randklev et al. 2010a, p. 297). From the
1960s to the 1990s, malacologists
working in central Texas found few
individuals and few new population
locations (Howells 2010d, p. 6).
Historical records suggest the Texas
fawnsfoot inhabited much of the
Colorado River, from Wharton County
upstream as far as the North Fork
Concho River in Sterling County, as
well as throughout the Concho, San
Saba, and Llano Rivers and Onion Creek
within the Colorado River basin
(Howells 2010d, p. 4; Randklev et al.
2010b, p. 24). In the Brazos River, the
species occurred from Fort Bend County
upstream to the lower reaches of the
Clear Fork Brazos River in Shackelford
County, as well as in the Leon River,
Little River, San Gabriel River, Deer
Creek, and Yegua Creek (Howells 2010d,
pp. 4–5; Randklev et al. 2010b, p. 24).
Species reports from the Trinity River
and other east Texas locations are of
misidentified fawnsfoot (Truncilla
donaciformis) (Howells 2010d, p. 4).
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Current Distribution
Relatively few Texas fawnsfoot have
been documented since this species was
first described in 1859, and very few
live individuals have been found in
recent decades (Randklev et al. 2010a,
p. 297). All of these animals were flood
deposited on gravel bars and near death
just prior to collection (Randklev et al.
2010a, p. 297), preventing information
from being gathered about population
size, preferred habitat, and other
parameters. A live population of Texas
fawnsfoot was not discovered until 2008
in the Brazos River near its confluence
with the Navasota River (Randklev et al.
2010a, p. 297). A second live population
was found in 2009 in the Colorado River
(Johnson 2009, p. 1). These two
locations contain the only confirmed
populations of the species to date.
Evidence of other remnant populations
has also been found in the Clear Fork
Brazos River, San Saba River, and Deer
Creek.
Colorado River System
The Texas fawnsfoot has been
eliminated from almost all of the
Colorado River system. Live individuals
were found in the lower mainstem
Colorado River in 2009, and the only
other evidence of current occurrence of
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Texas fawnsfoot in the Colorado River
basin is in the San Saba River, where a
population persists.
In the mainstem Colorado River, the
Texas fawnsfoot historically occurred
from Wharton County upstream into the
headwaters (Randklev et al. 2010c, p. 4;
OSUM 2011e, p. 1). Surveys throughout
the upper Colorado River between 1993
and 2009 yielded no evidence of Texas
fawnsfoot (Howells 1994, pp. 20–21, 29;
1996, pp. 20–21, 23; 1997a, pp. 27, 31,
34–35; 1998, p. 10; 2000a, p. 27; 2002a,
p. 6; 2004, p. 7; Burlakova and
Karatayev 2010a, p. 16), except for one
recently dead individual found in 1999
in San Saba County when the entire
river was dewatered and all mussels
were eliminated from the area (Howells
2000a, pp. 25–26; 2009, p. 17). The lack
of evidence of the species since that
time indicates that the population may
have been lost. In the lower Colorado
River in Colorado County, several old
shells of Texas fawnsfoot were found at
several sites in 1996 (Howells 1997a, p.
35), and, subsequently in 2009, two live
individuals were discovered (Johnson
2011, p. 1). The population was later
estimated to be approximately 2,800
individuals, with individuals ranging in
size from 21 to 38 mm (0.8–1.5 in)
(Burlakova and Karatayev 2010a, p. 17),
indicating that reproduction and
recruitment is occurring.
Texas fawnsfoot were not known to
occur in the San Saba River until a
single live individual was collected in
2011 (Burlakova and Karatayev 2011, p.
6). Additional surveys yielded 16 Texas
fawnsfoot of various ages collected at
the site (Randklev 2011b, p. 1),
indicating a persistent, recruiting
population.
Texas fawnsfoot is presumed
extirpated from the remainder of the
Colorado River basin. Although
historical records exist in the North
Concho, Concho, and Llano Rivers and
in Onion Creek (Randklev et al. 2010c,
p. 4), numerous surveys of these streams
indicate the extirpation of the species
(Howells 1994, pp. 5–6; 1995, pp. 22–
25, 28–29; 1996, pp. 21–22; 1998, pp.
14–17; 1999, pp. 15–16; 2000a, pp. 23,
25; 2001, p. 27; 2005, p. 9; Burlakova
and Karatayev 2011, p. 6).
Brazos River System
In the Brazos River system, the Texas
fawnsfoot persists in the mainstem
Brazos River, Clear Fork Brazos River,
Navasota River, and possibly in Deer
Creek. The species has been extirpated
from the Leon River, Little River, San
Gabriel River, and Yegua Creek.
In the mainstem Brazos River, the
Texas fawnsfoot historically occurred
throughout the length of the river, from
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Palo Pinto County downstream to Fort
Bend County (Randklev et al. 2010c, pp.
2–4; Burlakova and Karatayev 2010b, p.
1; OSUM 2011e, p. 1). While the species
appears to have retained its range
through the length of the Brazos River,
occurrences are represented by very few
live or recently dead individuals. In the
upper Brazos River in Palo Pinto and
Parker Counties, two live individuals
were found at each of two sites in 1996,
as well as numerous shells (Howells
1997a, pp. 16, 17). A survey in 2000
yielded no evidence of Texas fawnsfoot
in this area (Howells 2001, p. 19).
Nearby, in Somervell County, four
recently dead individuals were found in
the mainstem Brazos River in 1996
(Howells 1997a, pp. 18–19. In 2007,
only one old shell was found in the
same area (Burlakova and Karatayev
2010b, p. 1).
Surveys in Milam and Falls Counties
have not yielded any evidence of Texas
fawnsfoot, indicating the species has
been extirpated from this section of the
Brazos River (Howells 1995, p. 17; 1999,
pp. 12–13).
In the middle Brazos River, Texas
fawnsfoot persists in low numbers in
the vicinity of Brazos County. One live
individual was found in 1994 (Howells
1996, pp. 17–18), representing the first
live collection of the species anywhere
since the 1970s. In 1999, numerous
recently dead Texas fawnsfoot of mixed
sizes and ages were found at several
sites in Burleson and Brazos Counties
(Howells 2000a, pp. 21–22), indicating a
recruiting population existed in the
area. The species has been documented
here in repeated surveys in 2000, 2003,
and 2006 (Howells 2001, p. 22;
Karatayev and Burlakova 2008, p. 7;
Howells 2009, p. 17), indicating that the
species continues to persist in the area.
The first account of a living
population of Texas fawnsfoot (animals
living in situ rather than deposited on
or near the banks by floods) occurred in
2008 in the lower Brazos River near its
confluence with the Navasota River
(Randklev et al. 2010a, p. 297). Ten live
individuals were collected, and all were
small, indicating successful
reproduction and recent recruitment.
An additional Texas fawnsfoot was
found in this area in 2011 (Randklev
2011a, p. 1).
The farthest downstream collection of
Texas fawnsfoot in the Brazos River in
recent years was in Austin and Waller
Counties, when one live individual was
found in 2006 (Karatayev and Burlakova
2008, p. 39). It is likely the species
occurs sporadically through the section
of the Brazos River between Brazos and
Austin Counties.
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Texas fawnsfoot was first discovered
in the Navasota River in 2011, when
three individuals were found in
Washington and Grimes Counties
(Randklev 2011a, p. 1). Previous surveys
had not yielded evidence of the species
in this river (Howells 2001, p. 23).
In Deer Creek, a tributary to the
Brazos River in Falls County, a recently
dead Texas fawnsfoot was collected in
2006 (Burlakova and Karatayev 2010b,
p.1), despite previous surveys that
yielded no evidence of the species
(Howells 1999, p. 12).
Additionally, a Texas fawnsfoot
population persists in the Clear Fork
Brazos River. Recently dead Texas
fawnsfoot have been collected in several
locations along the length of the river,
in Shackelford, Stephens, and Young
Counties (Randklev et al. 2010c, p. 4;
Randklev 2011, pers. comm.). Several
other tributaries to the Brazos River that
historically contained Texas fawnsfoot
appear to no longer support the species
after numerous surveys reveal no living
or dead individuals, including the Leon
River (Howells 1994, pp. 18–20; 1997a,
pp. 19–20), the Little River (Howells
1997a, pp. 22–23), the San Gabriel River
(Howells 1997a, p. 23), and Yegua Creek
(Howells 1997a, pp. 24, 25–26; 1999, p.
14; 2001, p. 22; 2004, p. 6).
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Summary
The Texas fawnsfoot has declined
rangewide and is now known from only
five populations. The species has been
extirpated from nearly all of the
Colorado River basin and from much of
the Brazos River basin. Of the
populations that remain, only the
Colorado, San Saba, and Brazos River
populations are likely to be stable and
recruiting; the remaining populations
are disjunct and restricted to short
stream reaches.
Five-Factor Evaluation and Findings
Texas fatmucket, golden orb, smooth
pimpleback, Texas pimpleback, and
Texas fawnsfoot all occur in central
Texas across four major river basins
(Brazos, Colorado, Guadalupe, and
Nueces-Frio River basins). These species
depend on similar physical and
biological features and on the successful
functioning of riverine ecosystems to
survive. Many of the species face the
same or very similar threats. For each
species, we identified and evaluated all
the factors that may be threatening the
species. However, to avoid redundancy
of information when the analysis of the
threats is the same between species, we
referenced the reader to the initial
description of the common threats. For
example, the degradation of habitat and
habitat loss due to dams and
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regime, scouring and erosion of stream
channels, reduced dissolved oxygen
levels and water temperatures, and
changes in resident fish assemblages
(Williams et al. 1992, p. 7; Layzer et al.
1993, p. 69; Neves et al. 1997, pp. 63–
64; Pringle et al. 2000, pp. 810–815;
Watters 2000, pp. 265–266). Numerous
Five-Factor Evaluation for Texas
dams have been constructed throughout
Fatmucket
the Colorado, Guadalupe, Brazos, and
Information pertaining to the Texas
Nueces-Frio River systems within the
fatmucket in relation to the five factors
range of all five mussels addressed in
provided in section 4(a)(1) of the Act is
this finding (Stanley et al. 1990, p. 61).
discussed below.
Population losses due to the effects of
Factor A. The Present or Threatened
dams and impoundments have likely
Destruction, Modification, or
contributed more to the loss of diversity
Curtailment of Its Habitat or Range.
and abundance of freshwater mussels
The decline of mussels in Texas and
across Texas, including the Texas
across the United States is primarily the fatmucket, than any other factor. Stream
result of habitat loss and degradation
habitat throughout nearly all of the
(Neves 1991, pp. 252, 265; Howells et al. range of Texas fatmucket has been
1996, pp. 21–22). Chief among the
affected by numerous impoundments,
causes of mussel decline in Texas are
leaving generally short, isolated patches
the effects of impoundments,
of remnant habitat between dams.
sedimentation, dewatering, sand and
Impoundments have resulted in
gravel mining, and chemical
profound changes to the nature of the
contaminants (Neck 1982a, pp. 33–35;
rivers, primarily replacing free-flowing
Howells et al. 1996, pp. 21–22;
river systems with a series of large
Winemiller et al. pp. 17–18). These
reservoirs.
threats are discussed below.
There are no natural lakes within the
range of the Texas fatmucket, nor has it
Impoundments
ever been found in reservoirs. Surveys
A major factor in the decline of
of the reservoirs on the Guadalupe and
freshwater mussels across the United
Colorado Rivers have been ongoing
States has been the large-scale
since at least 1992, and no evidence of
impoundment of rivers (Vaughn and
live or dead Texas fatmucket has been
Taylor 1999, p. 913). Dams are the
found in any reservoir (Howells 1994,
source of numerous threats to
pp. 1–20; 1995, pp. 1–50; 1996, pp. 1–
freshwater mussels: They block
45; 1997a, pp. 1–58; 1998, pp. 1–30;
upstream and downstream movement of 1999, pp. 1–34; 2000a, pp. 1–56; 2001,
species by blocking host fish movement; pp. 1–50; 2002a, pp. 1–28; 2003, pp. 1–
they eliminate or reduce river flow
42; 2004, pp. 1–48; 2005, pp. 1–23;
within impounded areas, thereby
2006, pp. 1–106; Karatayev and
trapping silts and causing sediment
Burlakova 2008, pp. 1–47; Burlakova
deposition; and dams change
and Karatayev 2010a, pp. 1–30; 2011,
downstream water flow timing and
pp. 1–8), further indicating this species
temperature, decrease habitat
is not tolerant of impoundments.
heterogeneity, and affect normal flood
Impoundments occur throughout the
patterns (Layzer et al. 1993, pp. 68–69;
range of the Texas fatmucket. The
Neves et al. 1997, pp. 63–64; Watters
majority of the Nueces-Frio, Guadalupe,
2000, pp. 261–264; Watters 1996, p. 80). San Antonio, Colorado, and Brazos
Within reservoirs (the impounded
Rivers, as well as many tributaries, are
waters behind dams), the decline of
now impounded. There are 31 major
freshwater mussels has been attributed
reservoirs within the Colorado River
to sedimentation, decreased dissolved
basin, with another reservoir
oxygen, and alteration of resident fish
(Goldthwaite Reservoir) being
populations (Neves et al. 1997, pp. 63–
considered on the Colorado River in
64; Pringle et al. 2000, pp. 810–815;
Mills and San Saba Counties; this
Watters 2000, pp. 261–264). Dams
reservoir was the number one
recommendation in the water plan for
significantly alter downstream water
the region (Texas Water Development
quality and stream habitats (Allan and
Board (TWDB) 2011, p. 4–85). There are
Flecker 1993, p. 36; Collier et al. 1996,
29 reservoirs throughout the Guadalupe
pp. 1, 7) resulting in negative effects to
River basin and 34 reservoirs
tailwater (the area downstream of a
throughout the San Antonio River basin,
dam) mussel populations (Layzer et al.
each with a storage capacity of 3000
1993, p. 69; Neves et al. 1997, p. 63;
acre-feet or more, and many smaller
Watters 2000, pp. 265–266). Below
reservoirs (Exelon 2010, p. 2.3–4). The
dams, mussel declines are associated
majority of the large dams were
with changes and fluctuation in flow
impoundments is a common threat to all
five species, so a full description of the
threat was provided for the Texas
fatmucket, and for the remaining species
the initial description was referenced
with species-specific information
provided, as available.
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constructed for power generation, flood
control, and water supply, primarily by
the Lower Colorado River and
Guadalupe-Blanco River Authorities,
beginning in the early twentieth century
(Guadalupe-Blanco River Authority
2011, p. 1; Lower Colorado River
Authority (LCRA) 2011a, p. 1). These,
and numerous smaller dams, occur
throughout the Colorado and Guadalupe
River basins and have resulted in
ongoing destruction and modification of
Texas fatmucket habitat and the
curtailment of its range.
Dams threaten freshwater mussels in
several ways. First, they can prevent the
movement of freshwater mussel host
fish. The overall distribution of mussels
is a function of the dispersal of their
hosts (Watters 1996, p. 83). For
example, Watters (1996, p. 80) found
that the distributions of the fragile
papershell (Leptodea fragilis) and pink
heelsplitter (Potamilus alatus) in five
midwestern rivers were determined by
the presence of low-head dams. These
dams were non-navigable (without
locks), lacked fish ladders, and varied in
height from 1 to 17.7 m (3 ft to 58 ft),
and the host fish could not disperse
through them. Although the distribution
of mussels may depend on many
ecological factors, the evidence
presented in Watters (1996, pp. 79–85)
illustrates that dams as small as 1 m (3
ft) high can limit the distribution of
mussels. There are many dams that
occur throughout the range of the Texas
fatmucket that lack fish ladders and may
be a barrier to the movement of fish
hosts and, therefore, the distribution of
mussels. Because the Texas fatmucket
populations are all separated by dams of
various sizes that are not passable by
fish, the mussel is unable to disperse
from its current occupied range through
host fish migration.
Dams also alter aquatic habitat within
the resulting impoundments. It is well
documented that many mussel species
that are adapted to flowing water stream
environments do poorly in the altered
aquatic conditions found within
impoundments (Williams et al. 1992, p.
7; Vaughn and Taylor 1999, p. 913).
Once a dam is constructed, the original
river channel upstream remains intact
but under much deeper water with
much lower velocities. As water
velocity decreases, water loses its ability
to carry sediment; sediment falls to the
substrate, eventually smothering
mussels that cannot adapt to soft
substrates (Watters 2000, p. 263). Over
time, the original mussel species
composition of the stream channel may
be eliminated or changed in favor of silttolerant species (Watters 2000, p. 264).
The mussel community may be altered
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from one with many different species to
a community dominated by one to
several very common species (Neck
1982b, p. 174). Texas fatmucket does
not occur in reservoirs, indicating it is
not tolerant of lentic conditions, and it
is now extirpated from impounded areas
where it occurred prior to inundation.
The inundation of stream habitat by
impoundments is a likely cause of the
reduction in the distribution of the
Texas fatmucket. The presence of the
impoundments has caused the
permanent loss of Texas fatmucket
habitat throughout its range.
The loss of seven freshwater mussel
species native to Texas, including Texas
fatmucket and golden orb, due to
impoundment construction was
documented on the Medina River (Neck
1989, p. 323). The Medina River was
impounded in 1913 by construction of
Medina Dam, and now only three
different species of mussels, all of
which are tolerant of lentic habitats,
occur in the impounded area. The
bottom of Medina Lake now consists of
moderate and steep limestone slopes
and excessive silt deposits, whereas
before it was most likely made up of a
combination of silt, sand, and gravel
substrates. Most mussels native to the
Medina River were unable to adapt to
the change in flowing water and
substrate conditions (Neck 1989, p.
323), including the Texas fatmucket,
which is no longer found in the river.
Mussels downstream of
impoundments are often affected
through changes in fish host
availability, water quality (particularly
lower water temperatures), habitat
structure, and stream channel scouring
(Vaughn and Taylor 1999, p. 916). The
release of cold water from the
hypolimnion (deeper and colder layer of
water in reservoirs) can decrease the
occurrence of fish species adapted to
warm water and increase the occurrence
of fish species adapted to colder water
(Edwards 1978, pp. 73–75). This
changes the species composition of
suitable host fish and may prevent
mussels from completing an essential
part of their reproductive cycle. This
has been demonstrated by the
extirpation of mussel species from
several rivers on the eastern seaboard of
the United States, which has been
linked to the disappearance of
appropriate host fish; the reintroduction
of the host fish to rivers has enabled
mussel species to recolonize areas (Kat
and Davis 1984, p. 174). In addition,
because mussel reproduction is
temperature dependent (Watters and
O’Dee 1999, pp. 455–456), it is likely
that individual mussels living in cold
waters downstream of dam releases may
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reproduce less frequently, if at all
(Layzer et al. 1993, p. 69). Low water
temperatures can also significantly
delay or prevent metamorphosis
(Watters and O’Dee 1999, pp. 454–455)
and glochidial release, which is often
triggered by water temperature (Watters
and O’Dee 2000, p. 136).
Similar changes in water temperatures
downstream of dams may be responsible
for the loss of some Texas fatmucket
populations. For example, Canyon
Reservoir on the Guadalupe River in
Comal County is a deep impoundment
built in 1964 that has hypolimnetic
water releases. Temperature monitoring
stations throughout the Guadalupe River
basin show that maximum temperatures
above Canyon Reservoir averaged 29.6
degrees Celsius (°C) (85.3 degrees
Fahrenheit (°F)); the maximum stream
temperatures below the reservoir
averaged only 19.7 °C (67.5 °F)
(Edwards 1978, p. 72). After
impoundment, dissolved oxygen and
water temperature dropped, with an
accompanying drop in mussel numbers
and species diversity (Young et al. 1976,
p. 216). According to historical museum
records analyzed by Randklev et al.
(2010b, pp. 1–32), the Texas fatmucket
once occurred in this area of the
Guadalupe River prior to the
construction of Canyon Reservoir. The
Guadalupe River and Canyon Lake in
Comal and Kendall Counties were
surveyed in 2009, and no live or
recently dead Texas fatmucket were
found (Burlakova and Karatayev 2010a,
pp. 12–13). We reasonably conclude
that the loss of the Texas fatmucket from
this area was caused by the changes to
the aquatic habitat of the Guadalupe
River from the effects of Canyon
Reservoir. Many of the dams throughout
the range of Texas fatmucket have
hypolimnetic water releases, including
Canyon Reservoir on the Guadalupe
River (Magnelia 2001, p. 1), and Inks
Lake, Lake LBJ (Schnoor and Fruh 1979,
p. 506), and Lake Travis (Texas Natural
Resource Conservation Commission
2001, p. 4) on the Colorado River,
among others. We anticipate that
changes in water temperatures from
water released by these and other
reservoirs also alter mussel habitats in
streams, causing the elimination of
mussel populations downstream.
In addition to the temperature of
water released from dams, highly
fluctuating, turbulent tailwaters devoid
of sediment will scour the riverbed
downstream of dams, rendering the area
without mussel habitat (Layzer et al.
1993, p. 69). Depending on the use of
the dam, water levels may fluctuate on
a regular interval (for hydroelectric
purposes) or at random (for flood
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control) (Watters 2000, p. 265). On the
Colorado River, Inks Lake, Lake Marble
Falls, Lake Buchanan, Lake Austin, Lake
Travis, and Lady Bird Lake are each
used for one or both of these purposes.
Mortality of another rare mussel species
in Texas, the Texas heelsplitter
(Potamilus amphichaenus) was
attributed to scheduled dewatering of
the Neches River below B.A. Steinhagen
Reservoir in east Texas (Neck and
Howells 1994, p. 15).
Fluctuating water levels below dams
also result in dramatic changes in water
velocity. Downstream of Lake
Livingston on the Trinity River in east
Texas, for example, high-volume water
discharges and abrupt stoppages of flow
resulted in a river bed composed of
large rocks and shifting sand (Neck and
Howells 1994, p. 14); these kinds of
habitat changes would be inhospitable
to Texas fatmucket below the dams
within its range. In some rivers this
unstable zone may be extensive. For
example, on the Brazos River
downstream of Possum Kingdom
Reservoir in Texas exhibited unstable
substrate for 150 km (240 mi) below the
dam (Yeager 1993, p. 68).
In one study of the downstream
effects of dams, Vaughn and Taylor
(1999, p. 915) found a strong, gradual,
linear increase in mussel species
richness and abundance at sites on the
Little River in Oklahoma downstream
from Pine Creek Reservoir. Their
research revealed that mussel species
richness and total abundance did not
begin to rebound until 20 km (12 mi)
downstream of the impoundment and
did not peak until 53 km (33 mi)
downstream. They noted the most
obvious difference since reservoir
construction has been the alteration of
the flow and temperature regimes,
which gradually return to preimpoundment levels with downstream
distance from the dam. These alterations
appear to have produced an extinction
gradient of mussels that is most severe
near the dam (Vaughn and Taylor 1999,
p. 915). We expect similar effects on the
Texas fatmucket and other Texas
mussels downstream of dams.
In one area on the Guadalupe River in
Kerr County, a Texas fatmucket
population once existed directly below
a small dam (Howells 1997a, p. 36),
indicating the effects of the dam
construction and closure were not
immediately lethal. However, the
population has been presumed
extirpated since 1998 (Howells 2006, p.
71), and it is likely that fluctuating
downstream flows from the dam
contributed to the loss of this
population.
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Dam construction also fragments the
range of Texas fatmucket, leaving
remaining habitats and populations
isolated by the structures as well as by
extensive areas of deep uninhabitable,
impounded waters. These isolated
populations are unable to naturally
recolonize suitable habitat that may be
impacted by temporary but devastating
events, such as severe drought, floods,
or pollution. Dams impound river
habitats throughout almost the entire
range of the species, and these
impoundments have left short and
isolated patches of remnant habitat,
typically between impounded reaches.
In summary, the widespread
construction of dams has affected the
Texas fatmucket throughout its range by
significantly altering stream habitat both
upstream and downstream of the dams
by changing fish assemblages, water
depths and velocities, water
temperature, dissolved oxygen,
substrate, and stream channels. The
effects of dams are ongoing and
continue to negatively impact the Texas
fatmucket rangewide. Because of this
loss of habitat and its effects on the
populations, we find that the effects of
impoundments are a threat to the Texas
fatmucket.
Sedimentation
Siltation and general sediment runoff
is a pervasive problem in streams and
has been implicated in the decline of
stream mussel populations (Ellis 1936,
pp. 39–40; Vannote and Minshall 1982,
p. 4105; Dennis 1984, p. ii; Brim Box
and Mossa 1999, p. 99; Fraley and
Ahlstedt 2000, pp. 193–194). Specific
biological effects on mussels from
excessive sediment include reduced
feeding and respiratory efficiency from
clogged gills (Ellis 1936, p. 40),
disrupted metabolic processes, reduced
growth rates, increased substrate
instability, limited burrowing activity
(Marking and Bills 1979, pp. 208–209;
Vannote and Minshall 1982, p. 4106),
physical smothering, and disrupted host
fish attractant mechanisms (Hartfield
and Hartfield 1996, p. 373). The primary
effects of excess sediment on mussels
are sublethal, with detrimental effects
not immediately apparent (Brim Box
and Mossa 1999, p. 101).
The physical effects of sediment on
mussel habitats are multifold and
include changes in suspended material
load; changes in streambed sediment
composition from increased sediment
production and runoff in the watershed;
changes in the form, position, and
stability of stream channels; changes in
water depth or the width-to-depth ratio,
which affects light penetration and flow
regime; actively aggrading (filling) or
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degrading (scouring) channels; and
changes in channel position that may
leave mussels stranded (Brim Box and
Mossa 1999, pp. 109–112).
Increased sedimentation and siltation
may explain, in part, why Texas
fatmucket appear to be experiencing
recruitment failure in some streams.
Interstitial spaces (small openings
between rocks and gravels) in the
substrate provide essential habitat for
juvenile mussels. When clogged with
sand or silt, interstitial flow rates and
spaces may become reduced (Brim Box
and Mossa 1999, p. 100), thus reducing
juvenile habitat availability. Juvenile
freshwater mussels, including Texas
fatmucket juveniles, burrow into
interstitial substrates, making it
particularly susceptible to degradation
of this habitat.
Even in 1959, both the Colorado and
Guadalupe Rivers were noted as having
high sedimentation rates from
agricultural activities (Soil Conservation
Service 1959, pp. 56, 59).
Approximately 40 percent of U.S. river
miles do not meet Clean Water Act
standards due to excessive sediment
loads (Environmental Protection Agency
(EPA) 2000, p. 1), with agricultural
activities being the primary source of
sediment in streams (Waters 1995, p.
170). In general, sedimentation,
resulting from unrestricted access by
livestock, has been shown to be a
significant threat to many streams and
their mussel populations (Fraley and
Ahlstedt 2000, p. 193). A primary land
use throughout the range of the Texas
fatmucket is grazing by cattle, sheep,
and goats (Hersh 2007, p. 11). Soil
compaction, which reduces vegetative
growth, from intensive grazing may
reduce infiltration rates and increase
runoff and erosion, and trampling of
riparian vegetation increases the
probability of erosion (Armour et al.
1994, p.10; Brim Box and Mossa 1999,
p. 103).
Another cause of increased sediments
in streams is widespread brush removal,
such as that of the native plant,
Juniperus ashei (Ashe juniper),
throughout central Texas. Juniperus
ashei removal can cause a marked
increase in sediment runoff into streams
(Greer 2005, p. 76). The Texas State Soil
and Water Conservation Board has a
funding program specifically for
Juniperus ashei removal in Blanco,
Gillespie, Kerr, Kendall, and Travis
Counties (Gillespie County Soil and
Water Conservation District 2011, p. 1),
which includes the watersheds of three
known Texas fatmucket populations in
Live Oak Creek, Threadgill Creek, and
the upper Guadalupe River. In one
example, Howells (2010f, p. 6) noted
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increased sediment deposition after
widespread Juniperus ashei removal
upstream of the Texas fatmucket
population in Live Oak Creek.
Sedimentation may become an
increasing threat to the Texas fatmucket
in the Colorado and Guadalupe River
basins as the Austin and San Antonio
metro areas continue to expand.
Activities associated with urbanization,
such as road construction and increased
impervious surfaces (surfaces that do
not allow infiltration of rain water), can
be detrimental to stream habitats (Couch
and Hamilton 2002, p. 1). Runoff from
increased impervious surfaces increases
sediment loads in streams and
destabilizes stream channels (Pappas et
al. 2008, p. 151). Impervious surfaces
also result in channel instability by
accelerating stormwater runoff, which
increases bank erosion and bed
scouring, thereby further increasing
downstream sedimentation (Brim Box
and Mossa 1999, p. 103). While erosion
and sedimentation associated with road
construction may be temporary, the
existence of road crossings is shown to
have ongoing impacts to mussel habitat.
For example, in the Guadalupe River,
road crossings were found to cause a
long-term increase in sedimentation
both upstream and downstream, as
channel constriction reduced flow
upstream, causing sediment deposition,
and runoff from the road increased
sedimentation downstream (KeenZebert and Curran 2009, p. 301). Urban
development activities may also affect
streams and their mussel fauna where
adequate streamside buffers are not
maintained and erosion from adjacent
land is allowed to enter streams
(Brainwood et al. 2006, p. 511).
Large projects that reduce vegetative
cover within the watersheds supporting
Texas fatmucket populations can also
increase sedimentation flowing into
streams. For example, the Lower
Colorado River Authority Transmission
Services Corporation (LCRA TSC) is
proposing to construct two new 345kilovolt (kV) electric transmission line
facilities between Tom Green (in the
Colorado River basin near San Angelo)
and Kendall Counties (in the Guadalupe
River basin north of San Antonio) to
provide electrical power to
accommodate increased human
populations (Clary 2010, p. 1). All of the
proposed project routes occur within
the range of the Texas fatmucket. Two
proposed segments would cross through
Live Oak Creek, one through the San
Saba River, and one through the upper
Guadalupe River; all of these streams
contain populations of the Texas
fatmucket. The proposed project could
negatively affect Texas fatmucket
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habitat if construction or maintenance
of the transmission line requires
removal of vegetation within the
riparian zone and that removal results
in an increase in sediment runoff into
Live Oak Creek and the Guadalupe and
San Saba Rivers (Clary 2010, pp. 7, 9,
15). Similar infrastructure development
activities to accommodate Texas
population growth are expected to be
undertaken across the species’ range
and will likely lead to additional
sources of sediment in the streams
inhabited by the Texas fatmucket.
Streams occupied by Texas fatmucket
are subject to increasing levels of
sedimentation from agricultural
activities, instream sand and gravel
mining, vegetation removal, and
urbanization. All of these activities are
ongoing throughout the range of the
Texas fatmucket and are unlikely to
decrease, resulting in significant threats
to the Texas fatmucket.
Dewatering
River dewatering can occur in several
ways: Anthropogenic activities such as
surface water diversions and
groundwater pumping, and natural
events, such as drought. Surface water
diversions and groundwater pumping
can lower water tables, reducing river
flows and reservoir levels. When water
levels in streams and reservoirs are
lowered dramatically, it can result in
mussels being stranded and dying in
previously wetted areas. This is a
particular concern within and below
reservoirs where water levels are
managed for purposes that result in
water levels in the reservoir or
downstream to rise or fall in very short
periods of time, such as when
hydropower facilities release water
during peak energy demand periods.
Rivers can also be dewatered to expedite
construction activities, which happened
in the upper Guadalupe River in Kerr
County in 1998 for bridge construction;
numerous Texas fatmuckets were
exposed and desiccated (dried out and
died) (Howells 1999, pp. 18–19).
Drought can also severely affect Texas
fatmucket populations. For example,
near-record dry conditions in 2008,
followed by a pattern of below-normal
rainfall during the winter and spring of
2009, led to one of the worst droughts
in recorded history for most of central
Texas, including the range of the Texas
fatmucket (Nielsen-Gammon and
McRoberts 2009, p. 2). This drought’s
severity was exacerbated by abnormally
high air temperatures, a likely effect of
climate change, which has increased
average air temperatures in Texas by at
least 1 °C (1.8 °F) (Nielsen-Gammon and
McRoberts 2009, p. 22). The reservoirs
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within the Colorado River basin were
extremely low during this time due to
the drought (Clean Water Action 2011,
p. 1), as were river levels. Minimal to no
flow was recorded at numerous sites
within the basin (U.S. Geological Survey
(USGS) 2011a, p. 1). Four of the five
current sites of the Texas fatmucket may
have had very low flows during the
2009 drought, including populations in
the San Saba, Llano, Pedernales, and
Guadalupe Rivers (Howells 2010c, pp.
9–10). As low flows persist, mussels
face oxygen deprivation, increased
water temperature, and, ultimately,
stranding (Golladay et al. 2004, p. 501).
Only the Llano River has been surveyed
since 2009, and the species persists in
that river (Burlakova and Karatayev
2011, p. 1). Central Texas is currently
experiencing another extreme drought,
with rainfall between October 2010 and
July 2011 being the lowest on record
during those months (LCRA 2011c, p.
1), and the effects of this drought are
being observed but are not yet fully
known. As of the date of publication of
this finding, the Llano River has nearly
stopped flowing (Mashhood 2011, p. 1);
this has undoubtedly affected Texas
fatmucket populations in this river.
We do not know the extent of the
impacts of stream dewatering on the
Texas fatmucket; however, because this
species’ populations are so small and
isolated, the loss of numerous
individuals at a site can have dramatic
consequences to the population.
Hydropower facilities, construction,
surface water diversions, groundwater
pumping, and drought are occurring
throughout the range of the Texas
fatmucket; therefore, the effects of
dewatering are ongoing and unlikely to
decrease in the future, resulting in
significant threats to the Texas
fatmucket.
Sand and Gravel Mining
Sand and gravel mining (removing
bed materials from streams) has been
implicated in the destruction of mussel
populations across the United States
(Hartfield 1993, pp. 136–138). Sand and
gravel mining causes stream instability
by increasing erosion and turbidity (a
measure of water clarity) and causing
subsequent sediment deposition
downstream (Meador and Layher 1998,
pp. 8–9). These changes to the stream
can result in large-scale changes to
aquatic fauna, by altering habitat and
affecting spawning of fish, mussels, and
other aquatic species (Kanehl and Lyons
1992, pp. 4–11).
Sedimentation and increased
turbidity can accrue from instream
mining activities. In the Brazos River, a
gravel dredging operation was
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documented as depositing sediment as
far as 1.6 km (1 mi) downstream
(Forshage and Carter 1973, p. 697).
Accelerated streambank erosion and
downcutting of streambeds are common
effects of instream sand and gravel
mining, as is the mobilization of fine
sediments during sand and gravel
extraction (Roell 1999, p. 7).
Mining activities may threaten some
local Texas fatmucket populations.
Currently, one mining operation is
permitted near the population in Onion
Creek (TPWD 2008c, p. 1), and another
in the Llano River watershed in Kimble
County (TPWD 2008a, p. 1). The permits
allow for repeated removal of sand and
gravel at various instream locations.
Two additional mining operations occur
in historical habitat for the species—the
mainstem Colorado River (U.S. Army
Corps of Engineers (USACE) 2010, p. 2)
and Johnson Creek (TPWD 2007a, p. 1).
In areas where repeated mining
occurs, an upstream progression of
channel degradation and erosion (called
headcutting) can occur (Meador and
Layher 1998, p. 8). Headcutting may
move miles upstream in a zipper-like
fashion as the upper boundary of the
modified area collapses. Headcutting
can be found within the majority of
rivers and streams in Texas, including
within the Texas fatmucket’s current
and historical range (Kennon et al. 1967,
p. 22). Headcuts induced by sand and
gravel mining can cause dramatic
changes in streambank and channel
shape that may affect instream flow,
water chemistry and temperature, bank
stability, and siltation (Meador and
Layher 1998, p. 8), all of which are
harmful to freshwater mussels. Mussels
are particularly vulnerable to channel
degradation and sedimentation
processes associated with headcutting
due to their immobility (Pringle 1997,
p. 429).
In addition to headcutting, mines that
are located near stream channels are
subject to the gravel pit being captured
by the stream during flood events or due
to gradual channel migration (Simmang
and Curran 2006, p. 1). For example,
two gravel mines along the Colorado
River downstream of Austin were
inundated; one by stream channel
migration in 1984, one by stream
capture in 1991 (Simmang and Curran
2006, p. 1). Once captured by the
mainstem river, gravel mines contribute
large amounts of suspended sediment to
the river, causing additional turbidity
and sedimentation and further
degrading mussel habitat.
Two Texas fatmucket populations in
the mainstem Colorado River and
Johnson Creek may be currently affected
by sand and gravel mining. These
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activities occur over a long period of
time, destabilizing habitat and altering
substrates and banks both upstream and
downstream. Altered habitat will cause
a decrease in the likelihood of
recolonization by mussels after the
activity has been completed. Therefore,
the effects of sand and gravel mining are
an ongoing threat to the Texas
fatmucket.
Chemical Contaminants
Chemical contaminants are
ubiquitous throughout the environment
and are a major reason for the decline
of freshwater mussel species nationwide
(Richter et. al. 1997, p. 1081; Strayer et
al. 2004, p. 436; Wang et al. 2007a, p.
2029). Chemicals enter the environment
through both point and nonpoint
discharges, including spills, industrial
sources, municipal effluents, and
agriculture runoff. These sources
contribute organic compounds, heavy
metals, pesticides, herbicides, and a
wide variety of newly emerging
contaminants to the aquatic
environment. As a result, water quality
can be degraded to the extent that
mussel populations are adversely
affected.
Chemical and oil spills can be
especially devastating to mussels
because they may result in exposure of
a relatively immobile species to elevated
concentrations that far exceed toxic
levels. Acute and chronic exposure to
oil spills in freshwater systems is largely
understudied; therefore, little
information is available on effects of oil
spills on freshwater ecosystems (Harrel
1985, p. 223; Bhattacharyya et al. 2002,
p. 205). Oil is retained much longer in
marshes and other low-energy
environments, such as slow-moving
streams and rivers, than on wave-swept
coasts (Bhattacharyya et al. 2002, p.
205). Oils have been found in sediments
at low energy sites as much as 5 years
after the occurrence of spills, and they
may be released into the water column
long after the initial spill. Oil may have
various chronic effects on water-column
and benthic (bottom-dwelling) species.
These effects include sensory
disruption, behavioral and
developmental abnormalities, and
reduced fertility (Bhattacharyya et al.
2002, p. 205). Oil spilled on the water
surface may also limit oxygen exchange,
coat the gills of aquatic organisms, and
cause pathological lesions on
respiratory surfaces, thereby affecting
respiration in aquatic organisms. Effects
of oil on freshwater mussels may result
from oil settling on the sediment
surfaces and accumulating in the
sediment. This can prevent invertebrate
colonization (Bhattacharyya et al. 2002,
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p. 205). Complete recovery of benthic
communities may be a matter of years,
with communities in the meantime
consisting solely of pollutant-tolerant
organisms (Bhattacharyya et al. 2002, p.
205). Oil spills can occur from on-site
accidents (tank, pipeline spills) or from
tanker truck accidents within
watersheds occupied by Texas
fatmucket. For example, 450 gallons of
oil were spilled into Lake Bastrop, a
reservoir on a tributary to the Colorado
River, in February 2011 (Cihock 2011,
p. 1).
Exposure of mussels to persistent low
concentrations of contaminants likely to
be found in aquatic environments can
also adversely affect mussels and their
populations. Such concentrations may
not be immediately lethal, but over time
can result in mortality, reduced
filtration efficiency, reduced growth,
decreased reproduction, changes in
enzyme activity, and behavioral changes
to all mussel life stages (Naimo 1995,
pp. 351–352; Baun et al. 2008, p. 392).
Frequently, procedures that evaluate the
‘‘safe’’ concentration of an
environmental contaminant (for
example, national water quality criteria)
do not have data for freshwater mussel
species or do not consider data that are
available for freshwater mussels (March
et al. 2007, pp. 2066–2067, 2073).
One chemical that is particularly toxic
to early life stages of mussels is
ammonia. Sources of ammonia include
agricultural activities (animal feedlots
and nitrogenous fertilizers), municipal
wastewater treatment plants, and
industrial waste (Augspurger et al. 2007,
p. 2026), as well as precipitation and
natural processes (decomposition of
organic nitrogen) (Goudreau et al. 1993,
p. 212; Hickey and Martin 1999, p. 44;
Augspurger et al. 2003, p. 2569; Newton
2003, p. 2543). Therefore, ammonia is
considered a limiting factor for survival
and recovery of some mussel species
due to its ubiquity in aquatic
environments, high level of toxicity, and
because the highest concentrations
typically occur in mussel microhabitats
(Augspurger et al. 2003, p. 2574). In
addition, studies have shown that
ammonia concentrations increase with
increasing temperature and low-flow
conditions (Cherry et al. 2005, p. 378;
Cooper et al. 2005, p. 381), which may
be exacerbated during low-flow events
in streams. Within the range of Texas
fatmucket, high ammonia levels are
common, either chronically, such as in
Elm Creek, which is listed as impaired
due to high ammonia concentrations
(Texas Commission on Environmental
Quality (TCEQ) 2010a, p. 294), or due to
spills. A wastewater leak in August
2010 spilled approximately 380,000
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liters (L) (100,000 gallons (gal)) of
sewage into Elm Creek (Bramlette and
Cosel 2010, p. 1); ammonia is present in
high concentrations in sewage, among
other pollutants. Additionally, a sewage
spill in 2008 in Onion Creek discharged
nearly 380,000 L (100,000 gal), and
another sewage spill occurred in April
2011 in Quinlan Creek, a tributary to the
Guadalupe River near the Kerr County
population (MacCormack 2011, p. 1).
High ammonia levels from chronic
sources as well as from spills may be
affecting Texas fatmucket populations.
In addition to ammonia, agricultural
sources of chemical contaminants
include two broad categories that have
the potential to adversely affect mussel
species: Nutrients and pesticides. High
amounts of nutrients, such as nitrogen
and phosphorus, in streams can
stimulate excessive plant growth (algae
and periphyton, among others), which
in turn can reduce dissolved oxygen
levels when dead plant material
decomposes. Nutrient over-enrichment
in streams is primarily a result of runoff
of fertlizer and animal manure from
livestock farms, feedlots, and heavily
fertilized row crops (Peterjohn and
Correll 1984, p. 1471). Over-enriched
conditions are exacerbated by low-flow
stream conditions, such as those
experienced during typical summer
season flows. Bauer (1988, p. 244) found
that excessive nitrogen concentrations
can be detrimental to the adult
freshwater pearl mussel (Margaritifera
margaritifera), as was evident by the
positive linear relationship between
mortality and nitrate concentrations.
Also, a study of mussel life span and
size (Bauer 1992, p. 425) showed a
negative correlation between growth
rate and high nutrient concentrations,
and longevity was reduced as the
concentration of nitrates increased.
Juvenile mussels in interstitial habitats
are particularly affected by depleted
dissolved oxygen levels resulting from
nutrient over-enrichment (Sparks and
Strayer 1998, p. 133). The Texas
fatmucket occurs within the Concho
River watershed, which has been
documented as having particularly high
nitrates for nearly 20 years, likely due
to intensive agriculture in the area
(Texas Clean Rivers Program 2008, p. 2),
which may be affecting the Texas
fatmucket population.
Mussels are also affected by metals
(Keller and Zam 1991, p. 543) such as
cadmium, chromium, copper, mercury,
and zinc, which can negatively affect
biological processes such as growth,
filtration efficiency, enzyme activity,
valve closure, and behavior (Keller and
Zam 1991, p. 543; Naimo 1995, pp. 351–
355; Jacobson et al. 1997, p. 2390;
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Valenti et al. 2005, p. 1244). Metals
occur in industrial and wastewater
effluents and are often a result of
atmospheric deposition from industrial
processes and incinerators. Studies have
shown that copper can have toxic effects
on glochidia and juvenile freshwater
mussels (Wang et al. 2007a, pp. 2036–
2047; Wang et al. 2007b, pp. 2048–
2056). In the range of Texas fatmucket,
high copper concentrations have been
recorded in fish in the lower Guadalupe
River and San Antonio River (Lee and
Schultz 1994, p. 8). While these high
levels of copper in fish are not directly
informative of the level of copper within
the habitat of the Texas fatmucket, these
observations demonstrate that copper
levels are likely high in the lower
Guadalupe and San Antonio Rivers.
Because we know that copper
contamination in water can lead to
death of mussels, we conclude that the
copper may be adversely affecting Texas
fatmucket.
Mercury is another heavy metal that
has the potential to negatively affect
mussel populations, and it is widely
distributed in the environment. Mercury
has been detected throughout aquatic
environments as a product of municipal
and industrial waste and atmospheric
deposition from coal burning plants.
Rainbow mussel (Villosa iris) glochidia
have been demonstrated to be more
sensitive to mercury than juvenile
mussels, with the median lethal
concentration value of 14 parts per
billion (ppb) for glochidia, compared to
114 ppb for the juvenile life stages
(Valenti 2005, p. 1242). The chronic
toxicity tests conducted determined that
juveniles exposed to mercury greater
than or equal to 8 ppb exhibited
reduced growth. Acute mercury toxicity
was determined to be the cause of
extirpation of a diverse mussel
community for a 112 km (70 mi) portion
of the North Fork Holston River in
Virginia (Brown et al. 2005, pp. 1455–
1457). Mercury has been documented
throughout the Guadalupe and San
Antonio Rivers, with particularly high
concentrations in fish in the upper
reaches of both rivers (Lee and Schultz
1994, p. 8). As with copper, we do not
have information on the concentration
of mercury that Texas fatmucket is being
exposed to in these streams, but the
higher than expected levels in fish
indicate high mercury levels in the area,
which may be adversely affecting Texas
fatmucket.
Pesticides are another source of
contaminants in streams. Elevated
concentrations of pesticides frequently
occur in streams due to pesticide runoff,
overspray application to row crops, and
lack of adequate riparian buffers. The
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timing of agricultural pesticide
applications in the spring often
coincides with the reproductive and
early life stages of mussels, which may
increase the vulnerability of mussels to
pesticides (Bringolf et al. 2007a, p.
2094). Little is known regarding the
effect of currently used pesticides to
freshwater mussels even though some
pesticides, such as glyphosate (active
ingredient in Roundup®), are used
globally. Recent studies tested the
toxicity of glyphosate, its formulations,
and a surfactant (MON 0810) used in
several glyphosate formulations, to early
life stages of the fatmucket (Lampsilis
siliquoidea) (Bringolf et al. 2007a, p.
2094), a freshwater mussel closely
related to the Texas fatmucket. Studies
conducted with fatmucket juveniles and
glochidia determined that the surfactant
was the most toxic of the compounds
tested and that fatmucket glochidia were
the most sensitive organisms tested to
date (Bringolf et al. 2007a, p. 2094).
Roundup®, technical grade glyphosate
isopropylamine salt, and
isopropylamine were also acutely toxic
to juveniles and glochidia (Bringolf et
al. 2007a, p. 2097). These commonly
applied pesticides may be adversely
affecting Texas fatmucket populations.
The effects of other widely used
pesticides, including atrazine,
chlorpyrifos, and permethrin, on
glochidia and juvenile life stages have
also recently been studied (Bringolf et
al. 2007b, p. 2101). Environmentally
relevant concentrations (concentrations
that may be found in streams) of
permethrin and chlorpyrifos were found
to be toxic to glochidia and juvenile
fatmucket (Bringolf et al. 2007b, pp.
2104–2106). Commonly applied
pesticides are a threat to mussels as a
result of their widespread use. All of
these pesticides are commonly used on
agricultural lands throughout the range
of the Texas fatmucket, which may be
adversely affecting the species.
A potential, but undocumented, threat
to freshwater mussels, including Texas
fatmucket, are compounds referred to as
‘‘emerging contaminants’’ that are being
detected in aquatic ecosystems at an
increasing rate. These include
pharmaceuticals, hormones, and other
organic contaminants that have been
detected downstream from urban areas
and livestock production (Kolpin et al.
2002, p. 1202) and have been shown to
affect fish behavior (TCEQ 2010b, p. 3).
In samples of the Trinity River, for
example, compounds such as
antidepressants, antihistamines, blood
pressure lowering medication, antiseizure medication, and antimicrobial
compounds were all detected during a
2006 study (TCEQ 2010b, pp. 27–28). A
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large potential source of these emerging
contaminants is wastewater being
discharged through both permitted
(National Pollutant Discharge
Elimination System (NPDES)) and nonpermitted sites within the Colorado and
Guadalupe River systems. Although
streams within the range of Texas
fatmucket have not been tested for these
emerging contaminants, permitted
discharge sites are ubiquitous in
watersheds with Texas fatmucket
populations, providing many
opportunities for contaminants to
impact the species.
A study in the Blanco River found
that mussels may be adversely affected
by sewage effluent (Horne and McIntosh
1979, p. 132). Ammonia levels below
the outfall were three times higher than
the levels above the outfall and were
higher than recently determined toxicity
values of ammonia for mussels
(Augsperger et al. 2003, p. 2572). The
river was nutrient-enriched for miles
downstream, and mussels were less
abundant below the outfall than above
(Horne and McIntosh 1979, pp. 124–
125, 132). Texas fatmucket have not
been found alive in the Blanco River
since 1978.
Texas Commission on Environmental
Quality (TCEQ) data for 2010 indicated
that 26 of the 98 assessed water bodies
within the Texas fatmucket’s historical
and current range did not meet surface
water quality standards and were
classified as impaired water bodies
under the Clean Water Act (Texas Clean
Rivers Program 2010a, p. 5; 2010b, p.
13), including Elm Creek, due to high
ammonia. These water bodies were
impaired with dissolved solids, nitrates,
bacteria, low dissolved oxygen,
aluminum, sulfates, selenium, chloride,
and low pH associated with agricultural,
urban, municipal, and industrial runoff.
Of these, nitrates and low dissolved
oxygen pose the greatest threat to Texas
fatmucket, as discussed above. Chemical
contaminants, such as oil, ammonia,
copper, mercury, nutrients, pesticides,
and other compounds, are currently a
threat to the Texas fatmucket. The
species is vulnerable to acute
contamination from spills, which have
been documented in four of the seven
remaining populations, as well as
chronic contaminant exposure, which is
occurring rangewide.
Summary of Factor A
The reduction in numbers and range
of the Texas fatmucket is primarily the
result of the long-lasting effects of
habitat alterations such as the effects of
impoundments, sedimentation,
dewatering, sand and gravel mining,
and chemical contaminants.
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Impoundments occur throughout the
range of the species and have farreaching effects both up- and
downstream. Both the Colorado and
Guadalupe River systems have
experienced a large amount of
sedimentation from agriculture, mining,
urban development, and widespread
Juniperus ashei removal. Sand and
gravel mining affects Texas fatmucket
habitat by increasing sedimentation and
channel instability downstream and
causing headcutting upstream. Finally,
chemical contaminants have been
documented throughout the range of the
species and are significant concern to
Texas fatmucket. Based upon our review
of the best commercial and scientific
data available, we conclude that the
present or threatened destruction,
modification, or curtailment of its
habitat or range is an immediate threat
of high magnitude to the Texas
fatmucket.
Factor B. Overutilization for
Commercial, Recreational, Scientific, or
Educational Purposes.
The Texas fatmucket is not a
commercially valuable species and has
never been harvested in Texas as a
commercial mussel species (Howells
2010c, p. 11), although in the Llano
River shells were found that were
apparently collected by anglers for use
as bait (Howells 1996, p. 22; 2010c, p.
11). Additionally, the Elm Creek
population is suspected to have
declined in part due to the publication
of detailed location information, which
may have inspired collectors to visit the
site (Howells 2009, pp. 5–6). Scientific
collecting is not likely to be a significant
threat to the status of the species,
although disturbing gravid females can
result in glochidial loss and subsequent
reproductive failure. Additionally,
handling has been shown to reduce
shell growth in other mussel species,
including several other species of
Lampsilis (Haag and Commens-Carson
2008, pp. 505–506). Repeated handling
by researchers may adversely affect
Texas fatmucket individuals, but these
activities are occurring rarely and are
not likely to be a threat to populations.
Handling for scientific purposes
contributes to the long-term
conservation of the species.
We do not have any evidence of risks
to the Texas fatmucket from
overutilization for commercial,
recreational, scientific, or educational
purposes, and we have no reason to
believe this factor will become a threat
to the species in the future. Based upon
the best scientific and commercial
information available, we conclude that
overutilization for commercial,
recreational, scientific, or educational
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purposes does not pose a significant
threat to the Texas fatmucket.
Factor C. Disease and Predation.
Disease
Little is known about disease in
freshwater mussels. However, disease is
believed to be a contributing factor in
documented mussel die-offs in other
parts of the United States (Neves 1987,
pp. 11–12). Diseases have not been
documented or observed during any
studies of Texas fatmucket.
Predation
Raccoons have preyed on individual
Texas fatmuckets stranded by low
waters or deposited in shallow water or
on bars following flooding or low water
periods (Howells 2010c, p. 12).
Predation of Texas fatmucket by
raccoons may be occurring occasionally
but there is no indication it is a
significant threat to the status of the
species.
Some species of fish feed on mussels,
such as common carp (Cyprinus carpio),
freshwater drum, and redear sunfish
(Lepomis microlophus), all of which are
common throughout the range of Texas
fatmucket (Hubbs et al. 2008, pp. 19, 45,
53). Common species of flatworms are
voracious predators of newly
metamorphosed juvenile mussels of
many species (Zimmerman et al. 2003,
p. 30), including other species in the
genus Lampsilis (Delp 2002, pp. 12–13).
Predation is a normal aspect of the
population dynamics of a healthy
mussel population; however, predation
may amplify declines in small
populations.
Summary of Factor C
Disease in freshwater mussels is
poorly known, and we do not have any
information indicating it is a threat to
the Texas fatmucket. Additionally,
while predation is likely occurring
within Texas fatmucket populations, it
is a natural ecological interaction and
we have no information indicating the
extent of such predation is large enough
to be a threat to populations of Texas
fatmucket. Based upon the best
scientific and commercial information
available, we conclude that disease or
predation is not a threat to the Texas
fatmucket.
Factor D. The Inadequacy of Existing
Regulatory Mechanisms.
The Act requires us to examine the
adequacy of existing regulatory
mechanisms with respect to threats that
may place the Texas fatmucket in
danger of extinction or increase its
likelihood of becoming so in the future.
Existing regulatory mechanisms that
could affect threats to the Texas
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fatmucket include State and Federal
laws such as the Texas Threatened and
Endangered Species regulations, Texas
freshwater mussel sanctuaries, State and
Federal sand and gravel mining
regulations, and regulation of point and
non-point source pollution.
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Texas Threatened and Endangered
Species Regulations
On January 8, 2010, the Texas Parks
and Wildlife Commission placed 15
species of freshwater mussels, including
the Texas fatmucket, on the State
threatened list (Texas Register 2010, pp.
6–10). Section 68.002 of the Texas Parks
and Wildlife (TPW) Code and Section
65.171 of the Texas Administrative
Code (TAC) prohibit the direct take of
a threatened species, except under
issuance of a scientific collecting
permit. ‘‘Take’’ is defined in Section
1.101(5) of the TPW Code as collect,
hook, hunt, net, shoot, or snare, by any
means or device, and includes an
attempt to take or to pursue in order to
take. While this law protects individuals
from take, it is difficult to enforce and
does not provide any protection for
Texas fatmucket habitat. Moreover, our
assessment finds that the species is not
threatened by take (see Factor B above).
There are no State provisions under the
Texas Threatened and Endangered
Species Regulations for reducing or
eliminating the threats (see Factor A
above) that may adversely affect Texas
fatmucket or its habitat. In addition,
these State regulations do not call for
development of a recovery plan that will
restore and protect existing habitat for
the species. For these reasons, we find
that existing Texas regulatory
mechanisms for State-listed threatened
species are currently inadequate to
protect Texas fatmucket and its habitat
or to prevent further decline of the
species.
Freshwater Mussel Sanctuaries
The TPWD has designated specific
areas of streams and reservoirs as noharvest mussel sanctuaries (31 TAC,
part 2, chapter 57, subpart B, Rule
57.157). The locations of the designated
mussel sanctuaries were selected
because they support populations of
rare and endemic mussel species or are
important for maintaining, repopulating,
or allowing recovery of mussels in
watersheds where they have been
depleted. As a result of the designation
of mussel sanctuaries, four of the Texas
fatmucket populations are protected
from harvesting disturbance of other
species (Howells 2010f, p. 12).
Unfortunately, mussel sanctuaries only
restrict the harvest of mussels and do
not address other activities that may
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affect mussels or their habitats.
Therefore, these designations provide
no regulatory mechanisms to protect
Texas fatmucket from habitat alteration.
State Sand and Gravel Mining
Regulations
TPWD has been responsible for
regulating the ‘‘disturbance of taking’’
streambed materials since 1911 (Meador
and Layher 1998, p. 11) and has issued
several permits for ongoing activities
within the Texas fatmucket range (for
more information on the effects of sand
and gravel mining on Texas fatmucket,
please refer to ‘‘Sand and Gravel
Mining’’ under Factor A in Five-Factor
Evaluation for Texas Fatmucket). In
addition to authorized activities, there
are ongoing unauthorized sand and
gravel mining activities within the range
of Texas fatmucket. For example, the
LCRA, which monitors water quality
permit applications submitted through
other agencies (LCRA 2011b, p. 1),
found unpermitted sand removal from
the Llano River in Llano County during
a site visit in 2010 (Lehman 2010, p. 1).
This site is located upstream from a
known population of the Texas
fatmucket and other rare mussels
(Howells 1994, p. 6), and the sand
removal may have increased turbidity
and sedimentation downstream within
Texas fatmucket habitat. Sand and
gravel mining may be one of the least
regulated of all mining activities
(Meador and Layher 1998, p. 10).
Clean Water Act
The U.S. Army Corps of Engineers
(USACE) retains oversight authority and
requires a permit for gravel and sand
mining activities that deposit fill into
streams under section 404 of the Clean
Water Act (33 U.S.C. 1251 et seq.).
Additionally, a permit is required under
section 10 of the Rivers and Harbors Act
(33 U.S.C. 401 et seq.) for navigable
waterways. However, many mining
operations do not fall under these two
categories. For example, nationwide
permits are issued by the USACE for
types of projects that are presumed to
have minimal environmental impacts.
However, projects permitted by
nationwide permits, such as small
mining operations, may have
cumulative effects on aquatic species
like the Texas fatmucket through
increased sedimentation and channel
instability.
Point source discharges of potential
contaminants within the range of the
Texas fatmucket have been reduced
since the inception of the Clean Water
Act, but this reduction may not provide
adequate protection for filter-feeding
organisms that can be affected by
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extremely low levels of contaminants
(see ‘‘Chemical Contaminants’’ under
Factor A in the Five-Factor Evaluation
for Texas Fatmucket section). The EPA’s
established water quality criteria may
not be protective of mussels. Current
water quality standards applied by EPA
were established to be protective of
aquatic life; however, freshwater
mussels were not used to develop these
standards (EPA 2005, p. 5), and current
research reveals mussels to be more
sensitive to many aquatic pollutants
than the tested organisms (Augsperger et
al. 2007, p. 2025). For example,
Augspurger et al. (2003, p. 2572) and
Sharpe (2005, p. 28) suggested that the
criteria for ammonia may not be
sufficient to prevent impacts to mussels
under current and future climate
conditions. In addition, chronic copper
concentrations lethal to juvenile
freshwater mussels have been shown to
be less than the EPA’s 1996 chronic
water quality criterion for copper (Wang
et al. 2007b, pp. 2052–2055), and, as
stated above (see ‘‘Chemical
Contaminants’’ under Factor A in FiveFactor Evaluation for Texas Fatmucket),
high copper concentrations have been
documented in the lower Guadalupe
and San Antonio Rivers (Lee and
Schultz 1994, p. 8). Based on this
information, the existing EPA water
quality criteria may not be sufficient to
prevent negative effects to the Texas
fatmucket.
Nonpoint source pollution such as
sedimentation and chemical
contaminantation is considered a
significant threat to Texas fatmucket
habitat; however, the Clean Water Act
does not adequately protect Texas
fatmucket habitat from nonpoint source
pollution, because most activities that
cause nonpoint source pollution are not
regulated under the Clean Water Act.
Summary of Factor D
Despite some State and Federal laws
protecting the species and water quality,
the Texas fatmucket continues to
decline due to the effects of habitat
destruction, poor water quality,
contaminants, and other factors. The
regulatory measures described above are
not sufficient to significantly reduce or
remove the threats to the Texas
fatmucket. Based upon our review of the
best commercial and scientific data
available, we conclude that the lack of
existing regulatory mechanisms is an
immediate threat of moderate
magnitude to the Texas fatmucket.
Factor E. Other Natural or Manmade
Factors Affecting Its Continued
Existence.
Other natural and manmade factors
that threaten the Texas fatmucket
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include climate change, population
fragmentation and isolation, and
nonnative species.
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Climate Change
It is widely accepted that changes in
climate are occurring worldwide
(International Panel on Climate Change
(IPCC) 2007, p. 30). Understanding the
effects of climate change on the Texas
fatmucket is important because the
disjunct nature of the remaining Texas
fatmucket populations, coupled with
the limited ability of mussels to migrate,
makes it unlikely that the Texas
fatmucket can adjust its range in
response to changes in climate (Strayer
2008, p. 30). For example, changes in
temperature and precipitation can
increase the likelihood of flooding or
increase drought duration and intensity,
resulting in direct effects to freshwater
mussels like the Texas fatmucket (Hastie
et al. 2003, pp. 40–43; Golloday et al.
2004, p. 503). Because the range of the
Texas fatmucket has been reduced to
isolated locations with low population
numbers in small rivers and streams, the
Texas fatmucket is vulnerable to
climatic changes that could decrease the
availability of water or produce more
frequent scouring flood events. Indirect
effects of climate change may include
declines in host fish populations,
habitat reduction, and changes in
human activity in response to climate
change (Hastie et al. 2003, pp. 43–44).
For the next two decades, a warming
of about 0.2 °C (0.4 °F) per decade is
projected across the United States (IPCC
2007, p. 12), and hot extremes, heat
waves, and heavy precipitation and
flooding are expected to increase in
frequency (IPCC 2007, p. 18). As with
many areas of North America, central
Texas is projected to experience an
overall warming trend in the range of
2.5 to 3.3 °C (4.5 to 6 °F) over the next
50 to 200 years (Mace and Wade 2008,
p. 656). Even under lower greenhouse
gas emission scenarios, recent
projections forecast a 2.8 °C (5 °F)
increase in temperature and a 10
percent decline in precipitation in
central Texas by 2080–2099 (Karl et al.
2009, pp. 123–124). Based on our
current understanding of climate
change, air temperatures are expected to
rise and precipitation patterns are
expected to change in areas occupied by
the Texas fatmucket. Karl et al. (2009, p.
12) also suggests that climate change
impacts on water resources in the
southern Great Plains (including central
Texas) are expected as rising
temperatures and decreasing
precipitation exacerbate an area already
plagued by low rainfall, high
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temperatures, and unsustainable water
use practices.
One preliminary study forecasting the
possible hydrological impacts of climate
change on the annual runoff and its
seasonality in the upper Colorado River
watershed was conducted by CH2M
HILL (2008). In this initial evaluation,
four modeling scenarios (chosen to
represent a range of possible future
climatic conditions) were each run
under a 2050 and 2080 time scenario,
producing annual surface water runoff
estimates at multiple sites with stream
gages in the Colorado River basin. For
the 2050 scenarios, the results from all
four climate change scenarios predicted
significant decreases in annual runoff
totals compared to historic averages
(CH2M HILL 2008, pp. 7–30—7–32). For
the 2080 scenarios, one model predicted
increases in annual runoff; the other
three 2080 scenarios predicted
decreases in annual runoff (CH2M HILL
2008, pp. 7–30—7–33). The modeling
efforts from this study focus on annual
averages and cannot necessarily account
for the seasonal variations in flooding
events or long periods of drought.
However, the study demonstrates the
potential effects of climate change on
surface water availability, which is
forecasted to result in an overall decline
in stream flows in the region where the
Texas fatmucket occurs.
In summary, climate change could
affect the Texas fatmucket through the
combined effects of global and regional
climate change, along with the
increased probability of long-term
drought. Climate change exacerbates
threats such as habitat degradation from
prolonged periods of drought, increased
water temperature, and the increased
allocation of water for municipal,
agricultural, and industrial use. As
such, climate change, in and of itself,
may affect the Texas fatmucket, but the
magnitude and imminence (when the
effects occur) of the effects remain
uncertain. Based upon our review of the
best commercial and scientific data
available, we conclude that the effects of
climate change in the future will likely
exacerbate the current and ongoing
threats of habitat loss and degradation
caused by other factors, as discussed
above.
Population Fragmentation and Isolation
All of the remaining populations of
the Texas fatmucket are small and
geographically isolated and thus are
susceptible to genetic drift (change of
gene frequencies in a population over
time), inbreeding depression, and
random or chance changes to the
environment, such as toxic chemical
spills (Watters and Dunn 1995, pp. 257–
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258) or dewatering. Inbreeding
depression can result in death,
decreased fertility, smaller body size,
loss of vigor, reduced fitness, and
various chromosomal abnormalities
(Smith 1974, pp. 350). Despite any
evolutionary adaptations for rarity,
habitat loss and degradation increase a
species’ vulnerability to extinction
(Noss and Cooperrider 1994, pp. 58–62).
Numerous authors (including Noss and
Cooperrider 1994, pp. 58–62; Thomas
1994, p. 373) have indicated that the
probability of extinction increases with
decreasing habitat availability. Although
changes in the environment may cause
populations to fluctuate naturally, small
and low-density populations are more
likely to fluctuate below a minimum
viable population (the minimum or
threshold number of individuals needed
in a population to persist in a viable
state for a given interval) (Gilpin and
Soule 1986, pp. 25–33; Shaffer 1981, p.
131; Shaffer and Samson 1985, pp. 148–
150).
The Texas fatmucket was widespread
throughout much of the Colorado and
Guadalupe River systems when few
natural barriers existed to prevent
migration (via host species) among
suitable habitats. Construction of dams,
however, likely destroyed many Texas
fatmucket populations through drastic
habitat changes and isolated the
remnant populations from each other.
For fertilization, Texas fatmucket
females need an upstream male to
release sperm; populations with few
individuals reduce the likelihood that
females will be exposed to sperm while
siphoning. Therefore, recruitment
failure is a potential problem for many
small populations rangewide, a
potential condition exacerbated by its
reduced range and increasingly isolated
populations. If downward population
trends continue, further significant
declines in total Texas fatmucket
population size and consequent
reduction in long-term survivability
may soon become apparent.
The small, isolated nature of the
Texas fatmucket’s remaining
populations also increases the species’
vulnerability to stochastic (random)
natural events. When species are limited
to small, isolated habitats, as the Texas
fatmucket is, they are more likely to
become extinct due to a local event that
negatively effects the population
(McKinney 1997, p. 497; Minckley and
Unmack 2000, pp. 52–53; Shepard 1993,
pp. 354–357). While the populations’
small, isolated nature does not represent
an independent threat to the species, it
does substantially increase the risk of
extirpation from the effects of all other
threats, including those addressed in
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this analysis, and those that could occur
in the future from unknown sources.
Based upon our review of the best
commercial and scientific data
available, we conclude that
fragmentation and isolation of small
remaining populations of the Texas
fatmucket exacerbate ongoing threats to
the species throughout all of its range
and are expected to continue.
Nonnative Species
Various nonnative species of aquatic
organisms are firmly established within
the range of the Texas fatmucket and
pose a threat to the species. Golden
algae (Prymnesium parvum) is a
microscopic algae considered to be one
of the most harmful algal species to fish
and other gill-breathing organisms
(Lutz-Carrillo et al. 2010, p. 24). Golden
algae was first discovered in Texas in
1985 and is presumed to have been
introduced from western Europe (LutzCarrillo et al. 2010, p. 30). Since its
introduction, golden algae has been
found in Texas rivers and lakes,
including two lakes in central Texas
(Baylor University 2009, p. 1). Under
certain environmental conditions, this
algae can produce toxins that can cause
massive fish and mussel kills (Barkoh
and Fries 2010, p. 1; Lutz-Carrillo et al.
2010, p. 24). Evidence shows that
golden algae probably caused fish kills
in Texas as early as the 1960s, but the
first documented fish kill due to golden
algae in inland waters of Texas occurred
in 1985 on the Pecos River in the Rio
Grande basin (TPWD 2002, p. 1). The
range of golden algae has increased to
include portions of the Brazos and
Colorado River basins, among others,
and it has been responsible for killing
more than 8 million fish in the Brazos
River since 1981 and more than 2
million fish in the Colorado River since
1989 (TPWD 2010a, p. 1). Although
actual mussel kills in Texas due to
golden algae have not been recorded in
the past, the toxin can kill mussels.
Therefore, the elimination of host fish
and the poisonous nature of the toxin to
mussels make future golden algae
blooms a threat to the Texas fatmucket.
An additional nonnative species, the
zebra mussel (Dreissena polymorpha),
poses a potential threat to the Texas
fatmucket. This invasive species has
been responsible for the extirpation of
freshwater mussels in other regions of
the United States, including the Higgin’s
eye (Lampsilis higginsii) in Wisconsin
and Iowa (Service 2006, pp. 9–10).
Zebra mussels attach in large numbers
to the shells of live native mussels and
are implicated in the loss of entire
native mussel beds (Ricciardi et al.
1998, p. 615). This fouling impedes
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locomotion (both laterally and
vertically), interferes with normal valve
movements, deforms valve margins, and
essentially suffocates and starves the
native mussels by depleting the
surrounding water of oxygen and food
(Strayer 1999, pp. 77–80). Heavy
infestations of zebra mussels on native
mussels may overly stress the animals
by reducing their energy reserves. Zebra
mussels may also filter the sperm and
possibly glochidia of native mussels
from the water column, thus reducing
reproductive potential. Habitat for
native mussels may also be degraded by
large deposits of zebra mussel
pseudofeces (undigested waste material
passed out of the incurrent siphon)
(Vaughan 1997, p. 11).
Zebra mussels are not currently found
within the range of the Texas fatmucket.
However, a live adult zebra mussel was
first documented in Lake Texoma on the
Red River (on the north Texas border
with Oklahoma) in 2009 (TPWD 2009a,
p. 1). Since that time, additional zebra
mussels have been reported from Lake
Texoma, where they are now believed to
be well established (TPWD 2009c, p. 1).
Zebra mussels are likely to spread to
many other Texas reservoirs through
accidental human transport (Schneider
et al. 1998, p. 789). Although zebra
mussels tend to proliferate in reservoirs
or large pools, released zebra mussel
larvae, called veligers, float downstream
and attach to any hard surface available,
rendering downstream Texas fatmucket
populations extremely vulnerable to
attachment and fouling. Because zebra
mussels are so easily introduced to new
locations, the potential for zebra
mussels to continue to expand in Texas
and invade the range of the Texas
fatmucket is high. If this occurs, the
Texas fatmucket is vulnerable to zebra
mussel attachment and subsequent
deprivation of oxygen, food, and
mobility.
A molluscivore (mollusk eater), the
black carp (Mylopharyngodon piceus) is
a potential threat to the Texas
fatmucket. The species has been
commonly used by aquaculturists to
control snails or for research in fish
production in several States, including
Texas (72 FR 59019, October 18, 2007).
Black carp can reach more than 1.3 m
(4 ft) in length and 150 pounds (68
kilograms (kg)) (Nico and Williams
1996, p. 6). Foraging rates for a 4-yearold fish average 3 to 4 pounds (1.4 to1.8
kg) a day, indicating that a single
individual could consume 10 tons
(9,072 kg) of native mollusks over its
lifetime (Mississippi Interstate
Cooperative Resource Association
(MICRA) 2005, p. 1). Black carp can
escape from aquaculture facilities. For
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example, in 1994 30 black carp escaped
from an aquaculture facility in Missouri
during a flood. Other escapes into the
wild by non-sterile carp are likely to
occur. Because of the high risk to
freshwater mussels and other native
mollusks, the Service recently listed
black carp as an injurious species under
the Lacey Act (72 FR 59019, October 18,
2007), which prevents importations and
interstate transfer of this harmful
species, but does not prevent its release
into the wild once it is in the State. If
the black carp were to escape within the
range of the Texas fatmucket, it would
likely negatively affect native mussels,
including the Texas fatmucket.
Based upon our review of the best
commercial and scientific data
available, we conclude that golden algae
is an ongoing threat to the Texas
fatmucket, and other nonnative species,
such as zebra mussels and black carp,
are a potential future threat to the Texas
fatmucket that is likely to increase as
these exotic species expand their
occupancy within the range of the Texas
fatmucket.
Summary of Factor E
The effects of climate change, while
difficult to quantify at this time, are
likely to exacerbate the current and
ongoing threat of habitat loss caused by
other factors, and the small sizes and
fragmented nature of the remaining
populations render them more
vulnerable to extirpation. In addition,
nonnative species, such as golden algae,
currently threaten the Texas fatmucket,
and the potential introduction of zebra
mussels and black carp are potential
future threats. Based upon our review of
the best commercial and scientific data
available, we conclude that other
natural or manmade factors are
immediate threats of moderate
magnitude to the Texas fatmucket.
Finding for Texas Fatmucket
As required by the Act, we considered
the five factors in assessing whether
Texas fatmucket is threatened or
endangered throughout all of its range.
We examined the best scientific and
commercial information available
regarding the past, present, and future
threats faced by the Texas fatmucket.
We reviewed the petition, information
available in our files, and other
available published and unpublished
information, and we consulted with
recognized Texas fatmucket experts and
other Federal and State agencies.
This status review identified threats
to the Texas fatmucket attributable to
Factors A, D, and E. The primary threat
to the species is from habitat destruction
and modification (Factor A) from
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impoundments, which scour riverbeds,
thereby removing mussel habitat,
decrease water quality, modify stream
flows, and prevent fish host migration
and distribution of freshwater mussels,
as well as sedimentation, dewatering,
sand and gravel mining, and chemical
contaminants. Additionally, most of
these threats may be exacerbated by the
current and projected effects of climate
change (discussed in Factor E). Threats
to the Texas fatmucket and its habitat
are not being adequately addressed
through existing regulatory mechanisms
(Factor D). Because of the limited
distribution of this endemic species and
its lack of mobility, these threats are
likely to result in the extinction of the
Texas fatmucket in the foreseeable
future.
On the basis of the best scientific and
commercial information available, we
find that the petitioned action to list the
Texas fatmucket under the Act is
warranted. We will make a
determination on the status of the
species as threatened or endangered
when we complete a proposed listing
determination. When we complete a
proposed listing determination, we will
examine whether the species may be
endangered or threatened throughout all
of its range or whether the species may
be endangered or threatened in a
significant portion of its range.
However, as explained in more detail
below, an immediate proposal of a
regulation implementing this action is
precluded by higher priority listing
actions, and progress is being made to
add or remove other qualified species
from the Lists of Endangered and
Threatened Wildlife and Plants.
We reviewed the available
information to determine if the existing
and foreseeable threats render the Texas
fatmucket at risk of extinction now such
that issuing an emergency regulation
temporarily listing the species under
section 4(b)(7) of the Act is warranted.
We determined that issuing an
emergency regulation temporarily
listing the species is not warranted for
the Texas fatmucket at this time,
because we have not identified a threat
or activity that poses a significant risk,
such that losses to the species during
the normal listing process would
endanger the continued existence of the
entire species. However, if at any time
we determine that issuing an emergency
regulation temporarily listing Texas
fatmucket is warranted, we will initiate
this action at that time.
Listing Priority Number for Texas
Fatmucket
The Service adopted guidelines on
September 21, 1983 (48 FR 43098), to
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establish a rational system for utilizing
available resources for the highest
priority species when adding species to
the Lists of Endangered and Threatened
Wildlife and Plants or reclassifying
species listed as threatened to
endangered status. These guidelines,
titled ‘‘Endangered and Threatened
Species Listing and Recovery Priority
Guidelines,’’ address the immediacy
and magnitude of threats, and the level
of taxonomic distinctiveness by
assigning priority in descending order to
monotypic genera (genus with one
species), full species, and subspecies (or
equivalently, distinct population
segments of vertebrates).
As a result of our analysis of the best
available scientific and commercial
information, we have assigned the Texas
fatmucket a Listing Priority Number
(LPN) of 2, based on our finding that the
species faces threats that are of high
magnitude and are imminent. These
threats include habitat loss and
degradation from impoundments,
sedimentation, sand and gravel mining,
and chemical contaminants; other
natural or manmade factors such as
climate change, small, isolated
populations, and nonnative species; and
the fact that the threats to the species
are not being adequately addressed by
existing regulatory mechanisms. Our
rationale for assigning the Texas
fatmucket an LPN of 2 is outlined
below.
Under the Service’s guidelines, the
magnitude of threat is the first criterion
we look at when establishing a listing
priority. The guidance indicates that
species with the highest magnitude of
threat are those species facing the
greatest threats to their continued
existence. These species receive the
highest listing priority. We consider the
threats that the Texas fatmucket faces to
be high in magnitude. Habitat loss and
degradation from impoundments,
sedimentation, sand and gravel mining,
and chemical contaminants are
widespread throughout the range of the
Texas fatmucket and profoundly affect
its survival and recruitment. Remaining
populations are small, isolated, and
highly vulnerable to stochastic events.
Under our LPN guidelines, the second
criterion we consider in assigning a
listing priority is the immediacy of
threats. This criterion is intended to
ensure that the species facing actual,
identifiable threats are given priority
over those for which threats are only
potential or that are intrinsically
vulnerable but are not known to be
presently facing such threats. We
consider the threats to the Texas
fatmucket as described under Factors A,
D, and E in the Five-Factor Evaluation
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for Texas Fatmucket section to be
imminent because these threats have
affected the species in the past, are
ongoing, and will continue in the
foreseeable future. Habitat loss and
destruction have already occurred and
will continue as the human population
continues to grow in central Texas.
Texas fatmucket populations may
already be below the minimum viable
population requirement, which would
cause a reduction in the number of
populations and an increase in the
species’ vulnerability to extinction.
These threats are exacerbated by climate
change, which will increase the
frequency and magnitude of droughts.
Therefore, we consider these threats to
be imminent.
The third criterion in our Listing
Priority Number guidance is intended to
devote resources to those species
representing highly distinctive or
isolated gene pools as reflected by
taxonomy. The Texas fatmucket is a
valid taxon at the species level and,
therefore, receives a higher priority than
subspecies, but a lower priority than
species in a monotypic genus.
Therefore, we assigned Texas fatmucket
an LPN of 2.
We will continue to monitor the
threats to the Texas fatmucket and the
species’ status on an annual basis, and
should the magnitude or imminence of
the threats change, we will revisit our
assessment of the LPN.
While we conclude that listing the
Texas fatmucket is warranted, an
immediate proposal to list this species
is precluded by other higher priority
listings, which we address in the
Preclusion and Expeditious Progress
section below. Because we have
assigned the Texas fatmucket an LPN of
2, work on a proposed listing
determination for the species is
precluded by work on higher priority
listing actions with absolute statutory,
court-ordered, or court-approved
deadlines and final listing
determinations for those species that
were proposed for listing with funds
from Fiscal Year (FY) 2011. This work
includes all the actions listed in the
tables below under Preclusion and
Expeditious Progress.
Five-Factor Evaluation for Golden Orb
Information pertaining to the golden
orb in relation to the five factors
provided in section 4(a)(1) of the Act is
discussed below.
Factor A. The Present or Threatened
Destruction, Modification, or
Curtailment of Its Habitat or Range.
As discussed above, the decline of
mussels in Texas and across the United
States is primarily the result of habitat
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loss and degradation. Chief among the
causes of decline of the golden orb in
Texas are the effects of impoundments,
dewatering, sedimentation, sand and
gravel mining, chemical contaminants,
and off-road vehicle use. These threats
are discussed below.
Impoundments
For general information on the effects
of impoundments on freshwater
mussels, please refer to
‘‘Impoundments’’ under Factor A in
Five-Factor Evaluation for Texas
Fatmucket. Golden orb occur in one
impoundment, Lake Corpus Christi,
indicating that inundation may not be as
detrimental to this species as it is to
other, more flow-dependent mussel
species. However, dams continue to
fragment golden orb populations. There
are 29 reservoirs, each with a storage
capacity of 3,000 acre-feet or more,
within the Guadalupe River basin and
34 within the San Antonio River basin,
in addition to many other smaller
reservoirs in these basins (Exelon 2010,
p. 2.3–4). Three large reservoirs exist
within the Nueces River basin.
Historical records showed that the
golden orb once occurred in the
Guadalupe River in Comal County
before the Canyon Reservoir was
constructed in 1964 (Randklev et al.
2010c, p. 4). No live or recently dead
golden orb have been found in this
reach since the reservoir was completed
(Burlakova and Karatayev 2010a, pp.
14–15), and we presume the species is
extirpated from this reach because of the
effects of the reservoir. Surveys of the
reservoirs in the Guadalupe River
system have been ongoing since at least
1992, and no evidence of live or dead
golden orb has been found in any of the
reservoirs (Howells 1994, pp. 1–20;
1995, pp. 1–50; 1996, pp. 1–45; 1997a,
pp. 1–58; 1998, pp. 1–30; 1999, pp. 1–
34; 2000a, pp. 1–56; 2001, pp. 1–50;
2002a, pp. 1–28; 2003, pp. 1–42; 2004,
pp. 1–48; 2005, pp. 1–23; 2006, pp. 1–
106; Karatayev and Burlakova 2008, pp.
1–47; Burlakova and Karatayev 2010a,
pp. 1–30; 2011, pp. 1–8).
For species such as golden orb that
may be able to survive the initial
inundation of reservoirs, conditions
within the reservoir are likely to become
uninhabitable. The deep water in
reservoirs is very cold and often devoid
of oxygen and necessary nutrients
(Watters 2000, p. 264). Cold water (less
than 11 °C (52 °F)) has been shown to
stunt mussel growth (Hanson et al.
1988, p. 352). Because mussel
reproduction is temperature dependent
(Watters and O’Dee 1999, p. 455), it is
likely that individuals living in the
constantly cold hypolimnion in these
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channels may never reproduce, or
reproduce less frequently (Watters 2000,
p. 264). Any golden orb that survived
the initial inundation may have been
unable to reproduce, eventually
eliminating the species from large areas
of the reservoir. The same would be true
for mussels living in cold-water
discharges downstream of large
impoundments (Watters 2000, p. 264).
Dam construction also fragments the
range of golden orb, leaving remaining
habitats and populations isolated by the
structures, as well as by extensive areas
of deep, uninhabitable, impounded
waters. These isolated populations are
unable to naturally recolonize suitable
habitat that may be impacted by
temporary but devastating events, such
as severe drought, chemical spills, or
unauthorized discharges. Dams
impound river habitats throughout
almost the entire range of the species.
These impoundments have left short
and isolated patches of remnant habitat,
typically in between impounded
reaches, such as the golden orb
population on the Guadalupe River
within about one mile (1.6 km)
downstream of Lake Wood. This
population is subject to dramatic flow
fluctuations from the hydroelectric
facility associated with the dam
(Howells 2010a, p. 4), which can leave
individuals stranded when water levels
are quickly lowered or wash individuals
downstream when flow is increased.
The widespread construction of dams
throughout the range of golden orb has
significantly altered stream habitat both
upstream and downstream of the dams
by changing fish assemblages,
temperature, dissolved oxygen, and
substrate. The effects of dams on the
golden orb are expected to be ongoing
decades after construction and are
presumed to be continuing today.
Because of this loss of habitat and its
widespread effects on the populations,
we conclude that the effects of dams are
a threat to the golden orb.
Sedimentation
For general information on the effects
of sedimentation on freshwater mussels
like the golden orb, please refer to
‘‘Sedimentation’’ under Factor A in
Five-Factor Evaluation for Texas
Fatmucket.
As with other freshwater mussel
species, the golden orb is affected by
excessive sedimentation in streams.
Even in 1959, the Guadalupe River was
noted as having high sedimentation
rates from agricultural activities (Soil
Conservation Service 1959, p. 59).
Turbidity has also been recorded as high
in the Guadalupe River near Victoria
(Exelon 2010, p. 2.3–186), indicating a
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large amount of suspended sediment
where a small golden orb population
was recently found. Sedimentation can
occur from agricultural activities, sand
and gravel mining, urban runoff, and
construction activities, among other
sources.
One example of a proposed project
that could lead to localized increases in
sedimentation within the range of the
golden orb is the LCRA TSC. This
project proposes to construct two new,
345-kV electric transmission line
facilities between Tom Green (in the
Colorado River basin near San Angelo)
and Kendall Counties (in the Guadalupe
River basin north of San Antonio) to
provide electrical power to
accommodate increased human
populations (Clary 2010, p. 1). One of
the proposed transmission lines would
cross the upper Guadalupe River in Kerr
County, which contains a small
population of golden orb. The proposed
project could negatively affect golden
orb habitat by clearing land within the
riparian zone and may increase
sediment runoff into the Guadalupe
River (Clary 2010, p. 7). Similar
activities to accommodate Texas
population growth are expected to be
undertaken across the species’ range
and will likely lead to additional
sources of sediment in the streams
inhabited by the golden orb.
Streams occupied by golden orb are
subject to increasing levels of
sedimentation from agriculture,
urbanization, and sand and gravel
mining. Agriculture is a common land
use in the Guadalupe and San Antonio
River basins. Sedimentation may
become an increasing threat to the
golden orb in the Guadalupe River basin
as the San Antonio metro area continues
to expand. Activities associated with
urbanization, such as road construction,
increased impervious surfaces, and road
construction can be detrimental to
stream habitats (Couch and Hamilton
2002, p. 1), and the City of San Antonio,
the second largest city in Texas,
continues to grow (City of San Antonio
2010, p. 5). Sedimentation from
agriculture, urbanization, and sand and
gravel mining is widespread in the
range of the golden orb will continue to
threaten the species.
Dewatering
River dewatering can occur in several
ways: anthropogenic activities such as
surface water diversions and
groundwater pumping, and natural
events, such as drought, which can
result in mussels stranded in previously
wetted areas. This is a particular
concern within and below reservoirs,
whose water levels are managed for
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various purposes that can cause water
levels in the reservoir or downstream to
rise or fall in very short periods of time,
such as when hydropower facilities
release water during peak energy
demand periods. For example, Lake
Corpus Christi reservoir has
experienced several drawdowns of lake
levels to reduce salinity levels in the
reservoir, such as in 1996 and 2006.
Golden orb have been stranded above
the water line during both drawdowns,
killing the exposed mussels (Howells
2006, pp. 75–76). Rivers can also be
dewatered to facilitate construction
activities, such as in the upper
Guadalupe River in Kerr County, which
was dewatered in 1998 for bridge
construction, which exposed and killed
golden orb (Howells 1999, pp. 18–19).
Drought can also severely impact
golden orb populations. Central Texas,
including the Guadalupe River basin,
experienced a major drought in the late
1970s (Lewis and Oliveria 1979, p. 243).
Near record dry conditions in 2008
followed by a pattern of below-normal
rainfall during the winter and spring of
2009 led to one of the worst droughts in
recorded history for most of central
Texas, including the range of the golden
orb (Nielsen-Gammon and McRoberts
2009, p. 2). This drought’s severity was
exacerbated by abnormally high air
temperatures, a likely effect of climate
change, which has already increased
average air temperatures in Texas by at
least 1 °C (1.8 °F) (Nielsen-Gammon and
McRoberts 2009, p. 22). The Guadalupe
River in Kerr County experienced
minimal to no flow during periods of
the 2009 drought (USGS 2011b, p. 2),
which may have negatively affected this
golden orb population. Central Texas is
currently experiencing another extreme
drought, with rainfall between October
2010 and July 2011 being the lowest on
record during those months (LCRA
2011c, p. 1); the effects of this drought
are being observed but are not yet fully
known.
We do not know the extent of the
impacts of stream dewatering on the
golden orb; however, because several
populations are small and isolated, the
loss of numerous individuals at a site
can have dramatic consequences to the
population. Hydropower facilities,
construction, and drought are occurring
throughout the range of the golden orb;
therefore, the effects of dewatering are
ongoing and unlikely to decrease,
resulting in significant threats to the
golden orb.
Sand and Gravel Mining
For general information on the effects
of sand and gravel mining on freshwater
mussels, please refer to ‘‘Sand and
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Gravel Mining’’ under Factor A in FiveFactor Evaluation for Texas Fatmucket.
In 1995, the reach of the Guadalupe
River near Victoria, which contains a
golden orb population, was described as
having numerous current and
abandoned sand and gravel mining
areas (USACE 1995, p. 7). Currently,
TPWD has permitted one sand mining
activity within the existing range of
golden orb, in the Guadalupe River
basin in Comal County (TPWD 2009b, p.
1); golden orb populations occur
upstream and downstream of this area
in the Guadalupe River. The permit
allows for the repeated removal of sand
and gravel at various locations within
the stream.
Headcuts from sand and gravel
mining operations have been
documented in the San Antonio River
basin in Karnes County from as early as
1967, with downstream channels having
steep, eroded banks (Kennon et al. 1967,
p. 22). The golden orb has not been
documented from this area since 1996,
and only an old, eroded shell was
collected at that time (Howells 1997a,
pp. 41–42).
The golden orb populations in the
Guadalupe River may be currently
threatened by sand and gravel mining.
These activities occur over a long period
of time, destabilizing habitat both
upstream and downstream, which
decreases the likelihood of
recolonization after the activity has been
completed. Therefore, the effects of sand
and gravel mining are an ongoing threat
to the golden orb.
Chemical Contaminants
For general information on the effects
of chemical contaminants on freshwater
mussels, please refer to ‘‘Chemical
Contaminants’’ under Factor A in FiveFactor Evaluation for Texas Fatmucket.
As with other freshwater mussel
species, the golden orb is also
threatened by chemical contaminants.
TCEQ water quality standards for 2010
indicated the majority of the assessed
water bodies within the golden orb’s
historical and current range did not
meet surface water quality standards
and were classified as impaired water
bodies (Nueces River Authority 2010,
pp. 1–37; Texas Clean Rivers Program
2010b, p. 13). These water bodies were
impaired with dissolved solids, nitrates,
bacteria, low dissolved oxygen, sulfates,
phosphates, chloride, chlorophyll-a, and
low pH associated with agricultural,
urban, municipal, and industrial runoff.
Of these, nitrates and low dissolved
oxygen pose the greatest threat to the
golden orb. Additionally, several
streams within the range of the golden
orb have been listed as impaired due to
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high ammonia concentrations, including
Elm Creek in the Guadalupe River basin
(TCEQ 2010a, p. 294). High copper
concentrations have been recorded in
the lower Guadalupe and San Antonio
Rivers (Lee and Schultz 1994, p. 8), and
mercury has been documented
throughout the Guadalupe and San
Antonio Rivers, with particularly high
concentrations found in fish tissues
from the upper reaches of both rivers
(Lee and Schultz 1994, p. 8). Row crop
agriculture and wastewater discharges
are prominant within the range of the
golden orb. These activities result in
chronic contamination from agricultural
pesticides and emerging contaminants
of rivers inhabited by the species and
are a threat to golden orb.
Numerous spills of potential
contaminant materials have occurred
within the range of the golden orb.
These can occur from on site accidents
(tank, pipeline spills) or from tanker
truck accidents within watersheds
occupied by golden orb. For example,
100,000 gallons of sewage spilled into
the San Antonio River near the City of
San Antonio when a pipeline collapsed
in October 2010 (San Antonio Water
System 2010, p. 1). The largest known
golden orb population occurs
downstream of this location. Raw
sewage contains very high ammonia
levels, which is toxic to freshwater
mussels, as well as other pollutants.
Additionally, 300 gallons of diesel fuel
spilled into the San Antonio River near
the same location in May 2011 (Serna
2011, p. 1). Another sewage spill
occurred in April 2011 in Quinlan
Creek, a tributary to the Guadalupe
River near the Kerr County population
of golden orb (MacCormack 2011, p. 1).
The actual effects on the golden orb of
spills such as these recent examples are
unknown, but there are likely to be
negative consequences.
Because of the risk of spills as well as
chronic contamination, chemical
contaminants, such as oil, ammonia,
copper, mercury, nutrients, pesticides,
and other compounds are currently a
threat to the golden orb. The species is
vulnerable to acute contamination from
spills as well as chronic contaminant
exposure, which is occurring rangewide.
Summary of Factor A
The reduction in numbers and range
of the golden orb is primarily the result
of the long-lasting effects of habitat
alterations such as the effects of
impoundments, sedimentation,
dewatering, sand and gravel mining,
and chemical contaminants.
Impoundments occur throughout the
range of the species and have farreaching effects both up- and
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downstream. Both the Colorado and
Guadalupe River systems experience a
large amount of sedimentation from
agriculture, instream mining, and urban
development. Sand and gravel mining
affects golden orb habitat by causing
headcutting upstream, increasing
sedimentation concentrations in the
water downstream, and causing channel
instability downstream. Chemical
contaminants have been documented
throughout the range of the species and
may represent a significant threat to the
golden orb. However, the large
populations in the middle and lower
Guadalupe River, lower San Antonio
River, and San Marcos River indicate
that some golden orb populations are
not currently as vulnerable to habitat
loss as others. Based upon our review of
the best commercial and scientific data
available, we conclude that the present
or threatened destruction, modification,
or curtailment of its habitat or range is
an immediate threat of moderate
magnitude to golden orb populations
rangewide.
Factor B. Overutilization for
Commercial, Recreational, Scientific, or
Educational Purposes.
The golden orb is not a commercially
valuable species and has never been
harvested in Texas as a commercial
mussel species (Howells 2010a, p. 12).
Some scientific collecting occurs but is
not likely to be a significant threat to the
species because it occurs only rarely.
However, handing mussels can disturb
gravid females and result in glochidial
loss and subsequent reproductive failure
(Waller et. al 1995, p. 205).
Additionally, handling has also been
shown to reduce shell growth across
mussel species, including several
species of Lampsilis (Haag and
Commens-Carson 2008, pp. 505–506).
Repeated handling by researchers may
adversely affect golden orb individuals,
but these activities are occurring rarely
and are not likely to threaten
populations. Handling for scientific
purposes contributes to the long-term
conservation of the species.
We do not have any evidence of risks
to the golden orb from overutilization
for commercial, recreational, scientific,
or educational purposes, and we have
no reason to believe this factor will
become a threat to the species in the
future. Based upon the best scientific
and commercial information available,
we conclude that overutilization of the
golden orb for commercial, recreational,
scientific, or educational purposes does
not pose a significant threat to the
species rangewide.
Factor C. Disease and Predation.
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Disease
Little is known about disease in
freshwater mussels. However, disease is
believed to be a contributing factor in
documented mussel die-offs in other
parts of the United States (Neves 1987,
pp. 11–12). Diseases have not been
documented or observed during any
studies of golden orb.
Predation
Raccoons will prey on freshwater
mussels stranded by low waters or
deposited in shallow water or on bars
following flooding or low water periods
(Howells 2010c, p. 12). Predation of
golden orb by raccoons may be
occurring occasionally but there is no
indication it is a significant threat to the
status of the species.
Some species of fish feed on mussels,
such as common carp, freshwater drum,
and redear sunfish, all of which are
common throughout the range of golden
orb (Hubbs et al. 2008, pp. 19, 45, 53).
Common species of flatworms are
voracious predators of newly
metamorphosed juvenile mussels of
many species (Zimmerman et al. 2003,
p. 30). Predation is a normal factor
influencing population dynamics of a
healthy mussel population; however,
predation may amplify declines in small
populations primarily caused by other
factors.
Summary of Factor C
Disease in freshwater mussels is
poorly known, and we do not have any
information indicating it is a threat to
the golden orb. Additionally, predation
is a natural ecological interaction and
we have no information indicating the
extent of any predation is a threat to
populations of golden orb. Based upon
the best scientific and commercial
information available, we conclude that
disease or predation is not a threat to
the golden orb.
Factor D. The Inadequacy of Existing
Regulatory Mechanisms.
Existing regulatory mechanisms that
could have an effect on threats to the
golden orb include State and Federal
laws such as Texas Threatened and
Endangered Species regulations and
freshwater mussel sanctuaries, State and
Federal sand and gravel mining
regulations, and regulation of point and
non-point source pollution. For more
information on the effects of these
regulations on the threats to freshwater
mussels in central Texas, please refer to
Factor D under Five-Factor Evaluation
for Texas Fatmucket.
Summary of Factor D
Despite State and Federal laws
protecting the species and water quality,
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the golden orb continues to decline due
to the effects of habitat destruction, poor
water quality, contaminants, and other
factors. The regulatory measures
described above have been insufficient
to significantly reduce or remove the
threats to the golden orb. Based upon
our review of the best commercial and
scientific data available, we conclude
that the lack of existing regulatory
mechanisms is an immediate threat of
moderate magnitude to the golden orb.
Factor E. Other Natural or Manmade
Factors Affecting Its Continued
Existence.
Natural and manmade factors that
threaten the golden orb include climate
change, population fragmentation and
isolation, and nonnative species.
Climate Change
For more general information on the
effects of climate change on freshwater
mussels in central Texas, please refer to
‘‘Climate Change’’ under Factor E in
Five-Factor Evaluation for Texas
Fatmucket. Because the range of the
golden orb has been reduced to isolated
locations, many with low population
numbers in small rivers and streams, the
golden orb is vulnerable to climatic
changes that could decrease the
availability of water.
The disjunct nature of the remaining
golden orb populations, coupled with
the limited ability of mussels to migrate,
makes it unlikely that golden orb can
adjust their range in response to changes
in climate (Strayer 2008, p. 30). Climate
change could affect the golden orb
through the combined effects of global
and regional climate change, along with
the increased probability of long-term
drought. Climate change exacerbates
threats such as habitat degradation from
prolonged periods of drought, increased
water temperature, and the increased
allocation of water for municipal,
agricultural, and industrial uses.
Climate change may be a significant
stressor that exacerbates existing threats
by increasing the likelihood of
prolonged drought. As such, climate
change, in and of itself, may affect the
golden orb, but the magnitude and
imminence of the effects remain
uncertain. Based upon our review of the
best commercial and scientific data
available, we conclude that the effects of
climate change in the future will likely
exacerbate the current and ongoing
threats of habitat loss and degradation
caused by other factors, as discussed
above.
Population Fragmentation and Isolation
For general information on the effects
of population fragmentation and
isolation on freshwater mussels in
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central Texas, please refer to
‘‘Population Fragmentation and
Isolation’’ under Factor E in Five-Factor
Evaluation for Texas Fatmucket. As
with many freshwater mussels, several
of the remaining populations of the
golden orb are small and geographically
isolated and thus are more susceptible
to genetic drift, inbreeding depression,
and random or chance changes to the
environment, such as toxic chemical
spills (Watters and Dunn 1995, pp. 257–
258) or dewatering. Historically, the
golden orb was widespread throughout
much of the Guadalupe River system
and in portions of the Nueces-Frio River
system when few natural barriers
existed to prevent migration (via host
species) among suitable habitats. The
extensive impoundment of the Nueces,
Guadalupe, and San Antonio River
basins by the construction of dams has
fragmented the few remaining golden
orb populations throughout these river
systems.
Small golden orb populations,
including those in Lake Corpus Christi
Reservoir, the upper Guadalupe River in
Kerr County, and the San Antonio River
in Victoria County, may now be below
the minimum population size required
to maintain population viability into the
future, since they are less likely to be
able to recover through recruitment
from events that reduce but do not
extirpate populations. Additionally,
these small populations are more
vulnerable to extirpation from stochastic
events, as the lack of connectivity
among populations does not permit
nearby populations to recolonize areas
affected by intense droughts, toxic
spills, or other isolated events that
result in significant mussel dieoffs.
While the small, isolated populations do
not represent an independent threat to
the species, the situation does
substantially increase the risk of
extirpation from the effects of all other
threats, including those addressed in
this analysis, and those that could occur
in the future from unknown sources.
Based upon our review of the best
commercial and scientific data
available, we conclude that
fragmentation and isolation of small
remaining populations of the golden orb
are occurring and are ongoing threats to
the species throughout all of its range.
Nonnative Species
For general information on the effects
of nonnative species on freshwater
mussels of central Texas, please refer to
‘‘Nonnative Species’’ under Factor E in
Five-Factor Evaluation for Texas
Fatmucket. Various nonnative aquatic
species pose a threat to the golden orb,
including golden algae, zebra mussels,
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and black carp. Zebra mussels and black
carp are not currently found within the
range of golden orb, but they are likely
to be introduced within its range in the
future.
Based upon our review of the best
commercial and scientific data
available, we conclude that golden algae
is an ongoing threat to the golden orb,
and other nonnative species, such as
zebra mussels and black carp, are a
potential threat to the golden orb that is
likely to increase as these exotic species
expand their occupancy to include the
range of the golden orb.
Summary of Factor E
The effects of climate change, while
difficult to quantify at this time, are
likely to exacerbate the current and
ongoing threat of habitat loss caused by
other factors, and the small sizes and
fragmented nature of the remaining
populations render them more
vulnerable to extirpation. In addition,
nonnative species, such as golden algae,
currently threaten the golden orb, and
the potential introduction of zebra
mussels and black carp are potential
future threats. Based upon our review of
the best commercial and scientific data
available, we conclude that other
natural or manmade factors are
immediate threats of moderate
magnitude to the golden orb.
Finding for Golden Orb
As required by the Act, we considered
the five factors in assessing whether the
golden orb is threatened or endangered
throughout all of its range. We
examined the best scientific and
commercial information available
regarding the past, present, and future
threats faced by the golden orb. We
reviewed the petition, information
available in our files, and other
available published and unpublished
information, and we consulted with
recognized golden orb experts and other
Federal and State agencies.
This status review identifies threats to
the golden orb attributable to Factors A,
D, and E. The primary threat to the
species is from habitat destruction and
modification (Factor A) from
impoundments, which scour riverbeds,
thereby removing mussel habitat,
decrease water quality, modify stream
flows, and restrict fish host migration
and distribution of freshwater mussels.
Additional threats under Factor A
include sedimentation, dewatering,
sand and gravel mining, and chemical
contaminants. Also, most of these
threats may be exacerbated by the
current and projected effects of climate
change, population fragmentation and
isolation, and the anticipated threat of
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nonnative species (discussed under
Factor E). Threats to the golden orb are
not being adequately addressed through
existing regulatory mechanisms (Factor
D). Because of the limited distribution
of this endemic species and its lack of
mobility, these threats are likely to lead
to the extinction of the golden orb in the
foreseeable future.
On the basis of the best scientific and
commercial information available, we
find that the petitioned action to list the
golden orb under the Act is warranted.
We will make a determination on the
status of the species as threatened or
endangered when we complete a
proposed listing determination. When
we complete a proposed listing
determination, we will examine
whether the species may be endangered
or threatened throughout all of its range
or whether the species may be
endangered or threatened in a
significant portion of its range.
However, as explained in more detail
below, an immediate proposal of a
regulation implementing this action is
precluded by higher priority listing
actions, and progress is being made to
add or remove qualified species from
the Lists of Endangered and Threatened
Wildlife and Plants.
We reviewed the available
information to determine if the existing
and foreseeable threats render the
golden orb at risk of extinction now
such that issuing an emergency
regulation temporarily listing the
species under section 4(b)(7) of the Act
is warranted. We determined that
issuing an emergency regulation
temporarily listing the species is not
warranted for the golden orb at this
time, because we have not identified a
threat or activity that poses a significant
risk, such that losses to the species
during the normal listing process would
endanger the continued existence of the
entire species. However, if at any time
we determine that issuing an emergency
regulation temporarily listing the golden
orb is warranted, we will initiate this
action at that time.
Listing Priority Number for Golden Orb
The Service adopted guidelines on
September 21, 1983 (48 FR 43098), to
establish a rational system for utilizing
available resources for the highest
priority species when adding species to
the Lists of Endangered and Threatened
Wildlife and Plants or reclassifying
species listed as threatened to
endangered status. These guidelines,
titled ‘‘Endangered and Threatened
Species Listing and Recovery Priority
Guidelines’’ address the immediacy and
magnitude of threats, and the level of
taxonomic distinctiveness by assigning
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priority in descending order to
monotypic genera (genus with one
species), full species, and subspecies (or
equivalently, distinct population
segments of vertebrates).
As a result of our analysis of the best
available scientific and commercial
information, we have assigned the
golden orb a Listing Priority Number
(LPN) of 8, based on our finding that the
species faces threats that are of
moderate magnitude and are imminent.
These threats include habitat loss and
degradation from impoundments,
sedimentation, sand and gravel mining,
and chemical contaminants; other
natural or manmade factors such as
climate change, small, isolated
populations, and nonnative species; and
the fact that the threats to the species
are not being adequately addressed by
existing regulatory mechanisms. Our
rationale for assigning the golden orb an
LPN of 8 is outlined below.
Under the Service’s guidelines, the
magnitude of threat is the first criterion
we look at when establishing a listing
priority. The guidance indicates that
species with the highest magnitude of
threat are those species facing the
greatest threats to their continued
existence. These species receive the
highest listing priority. We consider the
threats that the golden orb faces to be
moderate in magnitude. Habitat loss and
degradation from impoundments,
sedimentation, sand and gravel mining,
and chemical contaminants are
widespread throughout the range of the
golden orb, but several large
populations remain, including one that
was recently discovered, suggesting that
the threats are not high in magnitude.
Under our LPN guidelines, the second
criterion we consider in assigning a
listing priority is the immediacy of
threats. This criterion is intended to
ensure that the species facing actual,
identifiable threats are given priority
over those for which threats are only
potential or that are intrinsically
vulnerable but are not known to be
presently facing such threats. We
consider the threats to the golden orb as
described in Factors A, D, and E under
the Five-Factor Evaluation for Golden
Orb to be imminent because these
threats are ongoing and will continue in
the foreseeable future. Habitat loss and
destruction has already occurred and
will continue as the human population
continues to grow in central Texas.
Several golden orb populations may
already be below the minimum viable
population requirement, which would
cause a reduction in the number of
populations and an increase in the
species’ vulnerability to extinction.
These threats are exacerbated by climate
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change, which will increase the
frequency and magnitude of droughts.
Therefore, we consider these threats to
be imminent.
The third criterion in our Listing
Priority Number guidance is intended to
devote resources to those species
representing highly distinctive or
isolated gene pools as reflected by
taxonomy. The golden orb is a valid
taxon at the species level and, therefore,
receives a higher priority than
subspecies, but a lower priority than
species in a monotypic genus.
Therefore, we assigned golden orb an
LPN of 8.
We will continue to monitor the
threats to the golden orb and the
species’ status on an annual basis, and
should the magnitude or imminence of
the threats change, we will revisit our
assessment of the LPN.
While we conclude that listing the
golden orb is warranted, an immediate
proposal to list this species is precluded
by other higher priority listings, which
we address in the Preclusion and
Expeditious Progress section below.
Because we have assigned the golden
orb an LPN of 8, work on a proposed
listing determination for the species is
precluded by work on higher priority
listing actions with absolute statutory,
court-ordered, or court-approved
deadlines and final listing
determinations for those species that
were proposed for listing with funds
from Fiscal Year (FY) 2011. This work
includes all the actions listed in the
tables below under Preclusion and
Expeditious Progress.
Five-Factor Evaluation for Smooth
Pimpleback
Information pertaining to the smooth
pimpleback in relation to the five factors
provided in section 4(a)(1) of the Act is
discussed below.
Factor A. The Present or Threatened
Destruction, Modification, or
Curtailment of Its Habitat or Range.
As discussed above, the decline of
mussels in Texas and across the United
States is primarily the result of habitat
loss and degradation. Chief among the
causes of decline of the smooth
pimpleback in Texas are the effects of
impoundments, sedimentation,
dewatering, sand and gravel mining,
and chemical contaminants.
Impoundments
For general information on the effects
of impoundments on freshwater
mussels, please refer to
‘‘Impoundments’’ under Factor A in
Five-Factor Evaluation for Texas
Fatmucket. As with golden orb, smooth
pimpleback are able to tolerate some
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impoundment conditions. Smooth
pimpleback have been known to occur
in three mainstem reservoirs on the
Colorado River, although all but one
population is likely extirpated (Howells
1997a, pp. 32–33; 1999, p. 16; 2005, p.
8; 2006, p. 67). Dams continue to
fragment smooth pimpleback
populations, and the downstream effects
of dams are detrimental to smooth
pimpleback habitat. There are 74 major
reservoirs and numerous smaller
impoundments within the historical and
current range of the smooth pimpleback.
Thirty-one of the 74 major reservoirs are
located within the Colorado River basin
and the remaining 43 reservoirs are
located within the Brazos River basin.
There are also eleven new reservoirs
that have been recommended for
development as feasible alternatives to
meet future water needs within the
Brazos River basin (Brazos G Regional
Water Planning Group 2010, p. 4B.12–
1). In addition, six new off-channel
reservoirs are also being considered for
future development (Brazos G Regional
Water Planning Group 2010, p. 4B.13–
2). At least one of the proposed reservoir
sites on the Little River in Milam
County is in the vicinity of where a
single live smooth pimpleback was
found in 2006 (Karatayev and Burlakova
2008, p. 6).
Dam construction fragments the range
of smooth pimpleback, leaving
remaining habitats and populations
isolated by the structures as well as by
extensive areas of deep, uninhabitable,
impounded waters. These isolated
populations are unable to naturally
recolonize suitable habitat that may be
impacted by temporary but devastating
events, such as severe drought, chemical
spills, or unauthorized discharges. Dams
impound river habitats throughout
almost the entire range of the species.
These impoundments have left short
and isolated patches of remnant habitat,
typically in between impounded
reaches. Habitat downstream of dams
may be impaired for many miles; in the
Brazos River downstream of Possum
Kingdom Reservoir, substrate was
unstable for 150 km (240 mi) below the
dam (Yeager 1993, p. 68).
For species such as smooth
pimpleback that may be able to survive
the initial inundation of reservoirs,
conditions within the reservoir are
likely to become uninhabitable. The
deep water in reservoirs is very cold and
often devoid of oxygen and necessary
nutrients (Watters 2000, p. 264). Cold
water (less than 11 °C (52 °F)) has been
shown to stunt mussel growth (Hanson
et al. 1988, p. 352). Because mussel
reproduction is temperature dependent
(Watters and O’Dee 1999, p. 455), it is
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likely that individuals living in the
constantly cold hypolimnion in these
channels may never reproduce, or
reproduce less frequently (Watters 2000,
p. 264). Any smooth pimpleback that
survived the initial inundation may
have been unable to reproduce,
eventually eliminating the species from
large areas of the reservoir. The same
would be true for mussels living in coldwater discharges downstream of large
impoundments (Watters 2000, p. 264).
The widespread construction of dams
throughout the range of smooth
pimpleback has significantly altered
stream habitat both upstream and
downstream of the dams by changing
fish assemblages, temperature, dissolved
oxygen, and substrate. The effects of
dams are ongoing, decades after
construction. In addition, the
construction of new reservoirs is also
being considered within the species’
range that could result in additional
habitat loss. Because of this loss of
habitat and its effects on the
populations, we conclude that the
effects of impoundments are a threat to
the smooth pimpleback.
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Sedimentation
For general information on the effects
of sedimentation on freshwater mussels,
please refer to ‘‘Sedimentation’’ under
Factor A in Five-Factor Evaluation for
Texas Fatmucket.
As with other freshwater mussel
species, the smooth pimpleback is also
threatened by sedimentation. The
dominant land use in the Colorado
River basin is grazing (Hersh 2007, p.
11). Soil compaction from intensive
grazing may reduce infiltration rates and
increase runoff, and trampling of
riparian vegetation increases the
probability of erosion (Armour et al.
1994, p. 10; Brim Box and Mossa 1999,
p. 103). Additionally, much of the
Brazos River basin is grazed or farmed
for row crops, which often contributes
large amounts of sediment to the basin
(Brazos River Authority 2007, p. 4).
Reservoir construction in the upper
portion of the basin has been attributed
with the erosion and subsequent
sedimentation of the lower river (USGS
2001, p. 30), as sediment-poor tailwaters
scour the riverbanks below the dam and
deposit sediment farther downstream. In
2004, sedimentation was high enough in
the Brazos River below Possum
Kingdom Reservoir to cause residents to
raise concerns to the Brazos River
Authority (Brazos River Authority 2006,
p. 2), and elevated suspended sediment
levels have been reported throughout
the basin (Brazos River Authority 2006,
p. 8).
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Sedimentation may become an
increasing threat to the smooth
pimpleback in the Colorado and Brazos
River basins as the Austin metropolitan
area continues to expand. Activities
associated with urbanization, such as
road construction, increased impervious
surfaces, and road construction can be
detrimental to stream habitats (Couch
and Hamilton 2002, p. 1). The City of
Austin, population approximately
800,000 people (Austin City Connection
2011, p. 1) lies within the Colorado
River basin, and 3.9 million people live
within the Brazos River basin (Brazos
River Authority 2007, p. 1). Both of
these basins have undergone substantial
urbanization providing sources of
increased sediment runoff into habitats
of the smooth pimpleback.
The range of the smooth pimpleback
receives sediment from increasing levels
of sedimentation from agriculture,
urbanization, and sand and gravel
mining; sedimentation is likely to
continue to threaten the smooth
pimpleback.
Dewatering
River dewatering can occur in several
ways: Anthropogenic activities such as
surface water diversions and
groundwater pumping, and natural
events, such as drought, which can
result in mussels stranded in previously
wetted areas. This is a particular
concern for smooth pimpleback within
and below reservoirs, where water
levels are managed for various purposes
that can cause water levels in the
reservoir or downstream to rise or fall in
very short periods of time, such as when
hydropower facilities release water
during peak energy demand periods.
The three impoundments on the
Colorado River with records of smooth
pimpleback all experience periodic
water level drawdowns, which may
have contributed to the species’
apparent extirpation from Inks Lake and
Lake Marble Falls. In fact, smooth
pimpleback have been found stranded
(which leads to death) after drawdowns
in both of these reservoirs (Howells
1996, p. 22; 1999, p. 16).
Drought can also severely impact
smooth pimpleback populations. For
example, the Little Brazos River, which
once contained a diverse and numerous
freshwater mussel community that
included smooth pimpleback (Gentner
and Hopkins 1966, p. 458), experienced
a severe drought from about 1950 to
1956 that reduced the river to a series
of small, stagnant pools. The results of
this habitat degradation from the low
water nearly eliminated the mussel
community and killed many smooth
pimpleback (Gentner and Hopkins 1966,
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p. 458). Later, central Texas, including
the Colorado and Brazos River basins,
experienced a major drought in the late
1970s (Lewis and Oliveria 1979, p. 243).
Near record dry conditions in 2008
followed by a pattern of below-normal
rainfall during the winter and spring of
2009 led to one of the worst droughts in
recorded history for most of central
Texas, including the range of the
smooth pimpleback (Nielsen-Gammon
and McRoberts 2009, p. 2). This
drought’s severity was exacerbated by
abnormally high air temperatures, a
likely effect of climate change, which
has already increased average air
temperatures in Texas by at least 1 °C
(1.8 °F) (Nielsen-Gammon and
McRoberts 2009, p. 22). Instream flows
throughout the Brazos River basin
during this drought were significantly
reduced (USGS 2011c, p. 1) and smooth
pimpleback populations in areas with
reduced water levels, such as in the
middle Brazos River, may have been
negatively affected. Central Texas is
currently experiencing another extreme
drought, with rainfall between October
2010 and July 2011 being the lowest on
record during those months (LCRA
2011c, p. 1); the effects of this drought
are being observed but are not yet fully
known. Droughts result in a decrease in
water depth and flow velocity in
streams inhabited by smooth
pimpleback, which reduces the
availability of food and dissolved
oxygen and reduces survivability. As
droughts persist, mussels face hypoxia,
elevated water temperature and,
ultimately, death due to stranding
(Golladay et al. 2004, p. 501).
Sand and Gravel Mining
For general information on the effects
of sand and gravel mining on freshwater
mussels, please refer to ‘‘Sand and
Gravel Mining’’ under Factor A in FiveFactor Evaluation for Texas Fatmucket.
The Brazos River has a long history of
sand mining, particularly in the lower
river, and channel morphology changes
have been attributed to destabilization
due to instream sand mining in the area
(USGS 2001, p. 27). The removal of sand
from within the river creates sediment
traps during periods of high flow, which
causes scouring and erosion
downstream (USGS 2001, p. 27). One
gravel dredging operation in the Brazos
River was documented depositing
sediment as far as 1.6 km (1 mile)
downstream (Forshage and Carter 1973,
p. 697). Accelerated stream bank erosion
and downcutting of streambeds are
common effects of instream sand and
gravel mining, as is the mobilization of
fine sediments during sand and gravel
extraction (Roell 1999, p. 7).
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Within the range of the smooth
pimpleback, TPWD has issued permits
for four current sand mining activities
within the Brazos River (Austin,
Bosque, and Fort Bend Counties)
(TPWD 2004, p. 1; 2007b, p. 1, 2008b,
p. 1; 2010b, p. 1). The permits allow for
the repeated removal of sand and gravel
at various locations within the Brazos
River. The lower Brazos River, where
these mining activities occur, contains
one of the more numerous populations
of smooth pimpleback.
The smooth pimpleback population in
the lower Brazos River may be currently
affected by sand and gravel mining.
These activities occur over a long period
of time, destabilizing mussel habitat
both upstream and downstream, which
decreases the likelihood of
recolonization after the activity has been
completed. Therefore, the effects of sand
and gravel mining are an ongoing threat
to the smooth pimpleback and are
expected to continue to occur
throughout the range of the species.
Chemical Contaminants
For general information on the effects
of chemical contaminants on freshwater
mussels, please refer to ‘‘Chemical
Contaminants’’ under Factor A in FiveFactor Evaluation for Texas Fatmucket.
As with other freshwater mussels, the
smooth pimpleback is also threatened
by chemical contaminants. TCEQ data
for 2010 indicated that 26 of the 98
assessed water bodies within Colorado
River basin and 81 of approximately 124
assessed water bodies within Brazos
River basin did not meet surface water
quality standards and were classified as
impaired water bodies (Texas Clean
Rivers Program 2010a, p. 5; TCEQ
2010c, pp. 1–106). These water bodies
were impaired with dissolved solids,
nitrites, nitrates, bacteria, low dissolved
oxygen, aluminum, sulfates, selenium,
chloride, orthophosphorus, phosphorus,
Chlorophyll a, and low pH associated
with agricultural, urban, municipal, and
industrial runoff. Of these, nitrites and
low dissolved oxygen are known to be
harmful to freshwater mussels.
Agricultural pesticides and emerging
contaminants are likely also present in
streams inhabited by smooth
pimpleback. There are 53 wastewater
treatment plants permitted to discharge
more than one million gallons per day
into the Brazos River basin (Valenti and
Brooks 2008, p. 12); the outfalls of these
treatment plants have not been tested to
determine if they contain contaminants
of note.
Examples of the exposure of smooth
pimpleback to chemical contaminants
include an event in 1993 when an
unknown substance was dumped into a
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segment of the Little Brazos River
upstream from a smooth pimpleback
population. This site once supported an
abundant and diverse number of mussel
species, including the smooth
pimpleback, but when it was revisited
in 1993, a massive die-off of freshwater
mussels had occurred (Howells 2010b,
p. 11). In another instance in 2010,
crude oil overflowed from a failed
storage tank into Keechi Creek in Leon
County, a tributary to the Navasota
River (National Response Center 2010,
p. 2). This location is near a small
population of smooth pimpleback and
upstream of one of the largest known
populations of the species.
Numerous other spills have occurred
within the range of the smooth
pimpleback. These occurred from onsite accidents (storage tank or pipeline
spills) or from tanker truck accidents
within watersheds occupied by smooth
pimpleback. For example, oil has
spilled into the Brazos River a number
of times. As much as 320,000 L (84,000
gal) of crude oil was spilled in the
Brazos River in Knox County in 1991
(Associated Press 1991, p. 1). In June
2010, flooding of holding ponds
adjacent to oil drilling operations leaked
oil into Thompson Creek and
subsequently into the Brazos River
(Lewis 2010, p. 1). Also, in July 2010,
oil pipelines burst and released
approximately 165 barrels of crude oil
into the upper Double Mountain Fork of
the Brazos River in Garza County (Joiner
2010, p. 1). Although no analyses were
conducted of the specific effects of these
spills on smooth pimpleback, we expect
that if the mussels are exposed to even
moderate levels of toxic chemical
contaminants, such as crude oil, adverse
effects (both direct mortality and
indirect effects to food source
availabity) are likely to occur.
Releases of chemical contaminants,
such as oil, ammonia, copper, mercury,
nutrients, pesticides, and other
compounds into the habitat of the
smooth pimpleback are an ongoing
threat to the smooth pimpleback. The
species is vulnerable to acute
contamination from spills, as well as
chronic contaminant exposure, which
has occurred and is expected to
continue to occur throughout the range
of the smooth pimpleback.
Summary of Factor A
The reduction in numbers and range
of the smooth pimpleback is primarily
the result of the long-lasting effects of
habitat alterations such as the effects of
impoundments, sedimentation,
dewatering, sand and gravel mining,
and chemical contaminants.
Impoundments occur throughout the
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range of the species and have farreaching effects to riverine habitat both
upstream and downstream of the dams.
Both the Colorado and Brazos River
systems have experienced a large
amount of sedimentation from
agriculture, instream mining, and urban
development. Sand and gravel mining
affects smooth pimpleback habitat by
increasing sedimentation and channel
instability downstream and by causing
headcutting upstream. Chemical
contaminants exceeding the standards
developed to support aquatic life have
been documented throughout the range
of the species and may represent a
significant threat to the smooth
pimpleback. However, the large
populations in the San Saba River,
lower Brazos River, Navasota River,
Leon River, and Yegua Creek indicate
that some smooth pimpleback
populations are not currently as
vulnerable to habitat loss as others.
Therefore, based upon our review of the
best commercial and scientific data
available, we conclude that the present
or threatened destruction, modification,
or curtailment of its habitat or range is
an immediate threat of moderate
magnitude to the smooth pimpleback.
Factor B. Overutilization for
Commercial, Recreational, Scientific, or
Educational Purposes.
The smooth pimpleback is not a
commercially valuable species and has
never been harvested in Texas as a
commercial mussel species (Howells
2010b, p.12). Some scientific collecting
occurs but is not likely to be a
significant threat to the species because
it occurs only rarely. However, handling
mussels can disturb gravid females and
result in glochidial loss and subsequent
reproductive failure. Additionally,
handling has also been shown to reduce
shell growth across mussel species,
including several species of Lampsilis
(Haag and Commens-Carson 2008, pp.
505–506). Repeated handling by
researchers may adversely affect smooth
pimpleback individuals, but these
activities are occurring rarely and are
not likely to be a threat to populations.
Handling for scientific purposes
contributes to the long-term
conservation of the species.
We do not have any evidence of risks
to the smooth pimpleback from
overutilization for commercial,
recreational, scientific, or educational
purposes, and we have no reason to
believe this factor will become a threat
to the species in the future. Based upon
the best scientific and commercial
information available, we conclude that
overutilization for commercial,
recreational, scientific, or educational
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Factor D under Five-Factor Evaluation
for Texas Fatmucket.
purposes does not pose a threat to the
smooth pimpleback rangewide.
Factor C. Disease and Predation.
Summary of Factor D
Disease
Little is known about disease in
freshwater mussels. However, disease is
believed to be a contributing factor in
documented mussel die-offs in other
parts of the United States (Neves 1987,
pp. 11–12). Diseases have not been
documented or observed during any
studies of smooth pimpleback.
Predation
Raccoons will prey on freshwater
mussels stranded by low waters or
deposited in shallow water or on bars
following flooding or low water periods
(Howells 2010c, p. 12). Predation of
smooth pimpleback by raccoons may be
occurring occasionally, but there is no
indication it is a significant threat to the
status of the species.
Some species of fish feed on mussels,
such as common carp, freshwater drum,
and redear sunfish, all of which are
common throughout the range of
smooth pimpleback (Hubbs et al. 2008,
pp. 19, 45, 53). Common species of
flatworms are voracious predators of
newly metamorphosed juvenile mussels
of many species (Zimmerman et al.
2003, p. 30). Predation is a normal factor
influencing the population dynamics of
a healthy mussel population; however,
predation may amplify declines in small
populations primarily caused by other
factors.
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Summary of Factor C
Disease in freshwater mussels is
poorly known, and we do not have any
information indicating it is a threat to
the smooth pimpleback. Additionally,
predation is a natural ecological
interaction and we have no information
indicating the extent of any predation is
a threat to populations of smooth
pimpleback. Based upon the best
scientific and commercial information
available, we conclude that disease or
predation is not a threat to the smooth
pimpleback.
Factor D. The Inadequacy of Existing
Regulatory Mechanisms.
Existing regulatory mechanisms that
could have an effect on threats to the
smooth pimpleback include State and
Federal laws such as Texas Threatened
and Endangered Species regulations and
freshwater mussel sanctuaries, State and
Federal sand and gravel mining
regulations, and regulation of point and
non-point source pollution. For more
information on the effects of State and
Federal laws on the threats to freshwater
mussels in central Texas, please refer to
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Despite State and Federal laws
protecting the species and water quality,
the smooth pimpleback continues to
decline due to the effects of habitat
destruction, poor water quality,
contaminants, and other factors. The
regulatory measures described under
Factor D in the Five-Factor Evaluation
for Texas Fatmucket have been
insufficient to significantly reduce or
remove the threats to the smooth
pimpleback. Based upon our review of
the best commercial and scientific data
available, we conclude that the lack of
existing regulatory mechanisms is an
immediate and ongoing threat of
moderate magnitude to the smooth
pimpleback.
Factor E. Other Natural or Manmade
Factors Affecting Its Continued
Existence.
Natural and manmade factors that
threaten the smooth pimpleback include
climate change, population
fragmentation and isolation, and
nonnative species.
Climate Change
For general information on the effects
of climate change on freshwater mussels
of central Texas, please refer to ‘‘Climate
Change’’ under Factor E in Five-Factor
Evaluation for Texas Fatmucket.
Because the range of the smooth
pimpleback has been reduced to
isolated locations, many with low
population numbers, in small rivers and
streams, the smooth pimpleback is
vulnerable to climatic changes that
could decrease the availability of water.
The disjunct nature of the remaining
smooth pimpleback populations,
coupled with the limited ability of
mussels to migrate, makes it unlikely
that smooth pimpleback can adjust their
range in response to changes in climate
(Strayer 2008, p. 30). Climate change
exacerbates threats to the smooth
pimpleback, such as habitat degradation
from prolonged periods of drought;
increased water temperature; and the
increased allocation of water for
municipal, agricultural, and industrial
uses The magnitude and imminence of
these effects, however, remain
uncertain. Based upon our review of the
best commercial and scientific data
available, we conclude that the effects of
climate change in the future will likely
exacerbate the current and ongoing
threats of habitat loss and degradation
caused by other factors, as discussed in
Factor A.
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Population Fragmentation and Isolation
For general information on the effects
of population fragmentation and
isolation on freshwater mussels of
central Texas, please refer to
‘‘Population Fragmentation and
Isolation’’ under Factor E in Five-Factor
Evaluation for Texas Fatmucket. As
with many freshwater mussels, several
of the remaining populations of the
smooth pimpleback are small and
geographically isolated and thus are
susceptible to genetic drift, inbreeding
depression, and random or chance
changes to the environment, such as
toxic chemical spills (Watters and Dunn
1995, pp. 257–258), or dewatering.
Historically, the smooth pimpleback
was widespread throughout much of the
Colorado and Brazos River systems
when few natural barriers existed to
prevent migration (via host species)
among suitable habitats. The extensive
impoundment of the Brazos and
Colorado River basins has fragmented
smooth pimpleback populations
throughout these river systems.
Small smooth pimpleback
populations, including those in Lake
LBJ Reservoir and the middle Brazos,
Little, and Little Brazos Rivers, may be
below the minimum population size
required to maintain population
viability into the future, therefore
making these populations more
vulnerable to extirpation since they are
less likely to be able to recover through
recruitment from events that reduce but
do not extirpate populations.
Additionally, these small populations
are more vulnerable to extirpation from
stochastic events, as the lack of
connectivity among populations does
not permit nearby populations to
recolonize areas affected by intense
droughts, toxic spills, or other isolated
events that result in significant mussel
die-offs. While the small, isolated
populations do not represent an
independent threat to the species, the
situation does substantially increase the
risk of extirpation from the effects of all
other threats, including those addressed
in this analysis, and those that could
occur in the future from unknown
sources.
Based upon our review of the best
commercial and scientific data
available, we conclude that
fragmentation and isolation of small
remaining populations of the smooth
pimpleback are occurring and are
ongoing threats to the species
throughout all of its range. Further,
stochastic events may play a magnified
role in extirpation of small, isolated
populations.
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Nonnative Species
For general information on the effects
of nonnative species on freshwater
mussels of central Texas, please refer to
‘‘Nonnative Species’’ in Factor E under
Five-Factor Evaluation for Texas
Fatmucket. As with other freshwater
mussels, the smooth pimpleback is
threatened by nonnative species.
Various nonnative aquatic species pose
a threat to the smooth pimpleback,
including golden algae, zebra mussels,
and black carp. Of these, golden algae
has been responsible for killing more
than eight million fish in the Brazos
River since 1981 and more than two
million fish in the Colorado River since
1989 (TPWD 2010a, p. 1). Although
mussel kills due to golden algae have
not been recorded, we expect golden
algae to negatively affect mussel
populations through loss of host fish
and direct toxicity. Zebra mussels and
black carp do not currently occur within
the range of the smooth pimpleback,
although both are found in Texas and
could be introduced to the Brazos and
Colorado Rivers in the forseeable future.
Based on population responses of other
mussel species that overlap with zebra
mussels and black carp in similar river
conditions, we conclude that the
introduction of zebra mussels or black
carp into the range of smooth
pimpleback would be devastating to the
species.
Based upon our review of the best
commercial and scientific data
available, we conclude that golden algae
is an ongoing threat to the smooth
pimpleback, and other nonnative
species, such as zebra mussels and black
carp, are a potential threat to the smooth
pimpleback that is likely to increase as
these exotic species expand their
occupancy to include the range of the
smooth pimpleback.
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Summary of Factor E
The effects of climate change, while
difficult to quantify at this time, are
likely to exacerbate the current and
ongoing threat of habitat loss caused by
other factors, and the small sizes and
fragmented nature of the remaining
populations render them more
vulnerable to extirpation. In addition,
nonnative species, such as golden algae,
currently threaten the Texas fatmucket,
and the potential introduction of zebra
mussels and black carp are potential
future threats. Based upon our review of
the best commercial and scientific data
available, we conclude that other
natural or manmade factors are
immediate and ongoing threats of
moderate magnitude to the smooth
pimpleback.
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Finding for Smooth Pimpleback
As required by the Act, we considered
the five factors in assessing whether the
smooth pimpleback is threatened or
endangered throughout all of its range.
We examined the best scientific and
commercial information available
regarding the past, present, and future
threats faced by the smooth pimpleback.
We reviewed the petition, information
available in our files, and other
available published and unpublished
information, and we consulted with
recognized smooth pimpleback experts
and other Federal and State agencies.
This status review identifies threats to
the smooth pimpleback attributable to
Factors A, D, and E. The primary threat
to the species is from habitat destruction
and modification (Factor A) from
impoundments, which scour riverbeds,
thereby removing mussel habitat,
decreases water quality, modifies stream
flows, and restricts fish host migration
and distribution of freshwater mussels.
Additional threats under Factor A
include sedimentation, dewatering,
sand and gravel mining, and chemical
contaminants. Also, most of these
threats may be exacerbated by the
current and projected effects of climate
change (discussed under Factor E).
Threats to the smooth pimpleback are
not being adequately addressed through
existing regulatory mechanisms (Factor
D). Because of the limited distribution
of this endemic species and its lack of
mobility, these threats are likely to lead
to the extinction of the smooth
pimpleback in the foreseeable future.
On the basis of the best scientific and
commercial information available, we
find that the petitioned action to list the
smooth pimpleback under the Act is
warranted. We will make a
determination on the status of the
species as threatened or endangered
when we complete a proposed listing
determination. When we complete a
proposed listing determination, we will
examine whether the species may be
endangered or threatened throughout all
of its range; or whether the species may
be endangered or threatened in a
significant portion of its range.
However, as explained in more detail
below, an immediate proposal of a
regulation implementing this action is
precluded by higher priority listing
actions, and progress is being made to
add or remove qualified species from
the Lists of Endangered and Threatened
Wildlife and Plants.
We reviewed the available
information to determine if the existing
and foreseeable threats render the
smooth pimpleback at risk of extinction
now such that issuing an emergency
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regulation temporarily listing the
species under section 4(b)(7) of the Act
is warranted. We determined that
issuing an emergency regulation
temporarily listing the species is not
warranted for the smooth pimpleback at
this time, because we have not
identified a threat or activity that poses
a significant risk, such that losses to the
species during the normal listing
process would endanger the continued
existence of the entire species. However,
if at any time we determine that issuing
an emergency regulation temporarily
listing the smooth pimpleback is
warranted, we will initiate this action at
that time.
Listing Priority Number for Smooth
Pimpleback
The Service adopted guidelines on
September 21, 1983 (48 FR 43098), to
establish a rational system for utilizing
available resources for the highest
priority species when adding species to
the Lists of Endangered and Threatened
Wildlife and Plants or reclassifying
species listed as threatened to
endangered status. These guidelines,
titled ‘‘Endangered and Threatened
Species Listing and Recovery Priority
Guidelines’’ address the immediacy and
magnitude of threats, and the level of
taxonomic distinctiveness by assigning
priority in descending order to
monotypic genera (genus with one
species), full species, and subspecies (or
equivalently, distinct population
segments of vertebrates).
As a result of our analysis of the best
available scientific and commercial
information, we have assigned the
smooth pimpleback an LPN of 8, based
on our finding that the species faces
threats that are of moderate magnitude
and are imminent. These threats include
habitat loss and degradation from
impoundments, sedimentation, sand
and gravel mining, and chemical
contaminants; other natural or
manmade factors such as climate
change, small, isolated populations, and
nonnative species; and the fact that the
threats to the species are not being
adequately addressed by existing
regulatory mechanisms. Our rationale
for assigning the smooth pimpleback an
LPN of 8 is outlined below.
We consider the threats that the
smooth pimpleback faces to be moderate
in magnitude. Habitat loss and
degradation from impoundments,
sedimentation, sand and gravel mining,
and chemical contaminants are
widespread throughout the range of the
smooth pimpleback, but several large
populations remain, including one that
was recently discovered, indicating the
threats are not high in magnitude.
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Under our LPN guidelines, the second
criterion we consider in assigning a
listing priority is the immediacy of
threats. We consider the threats to the
smooth pimpleback as described under
‘‘Factor A. The Present or Threatened
Destruction, Modification, or
Curtailment of Its Habitat or Range,’’
‘‘Factor D. The Inadequacy of Existing
Regulatory Mechanisms,’’ and ‘‘Factor
E. Other Natural Or Manmade Factors
Affecting Its Continued Existence’’
under the Five-Factor Evaluation for
Smooth Pimpleback to be imminent
because these threats are ongoing and
will continue in the foreseeable future.
Habitat loss and destruction has already
occurred and will continue as the
human population continues to grow in
central Texas. Several smooth
pimpleback populations may already be
below the minimum viable population
requirement, which would cause a
reduction in the number of populations
and an increase in the species’
vulnerability to extinction. These
threats are exacerbated by climate
change, which will increase the
frequency and magnitude of droughts.
Therefore, we consider these threats to
be imminent.
Thirdly, the smooth pimpleback is a
valid taxon at the species level and,
therefore, receives a higher priority than
subspecies, but a lower priority than
species in a monotypic genus.
Therefore, we assigned smooth
pimpleback an LPN of 8. We will
continue to monitor the threats to the
smooth pimpleback and the species’
status on an annual basis, and should
the magnitude or imminence of the
threats change, we will revisit our
assessment of the LPN.
While we conclude that listing the
smooth pimpleback is warranted, an
immediate proposal to list this species
is precluded by other higher priority
listings, which we address in the
Preclusion and Expeditious Progress
section below. Because we have
assigned the smooth pimpleback an LPN
of 8, work on a proposed listing
determination for the species is
precluded by work on higher priority
listing actions with absolute statutory,
court-ordered, or court-approved
deadlines and final listing
determinations for those species that
were proposed for listing with funds
from Fiscal Year (FY) 2011. This work
includes all the actions listed in the
tables below under Preclusion and
Expeditious Progress.
Five-Factor Evaluation for Texas
Pimpleback
Information pertaining to the Texas
pimpleback in relation to the five factors
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provided in section 4(a)(1) of the Act is
discussed below.
Factor A. The Present or Threatened
Destruction, Modification, or
Curtailment of Its Habitat or Range.
As discussed above, the decline of
mussels in Texas and across the United
States is primarily the result of habitat
loss and degradation. Chief among the
causes of decline of the Texas
pimpleback are the effects of
impoundments, sedimentation,
dewatering, sand and gravel mining,
and chemical contaminants. These
threats are discussed below.
Impoundments
For general information on the effects
of impoundments on freshwater
mussels, please refer to
‘‘Impoundments’’ in Factor A under
Five-Factor Evaluation for Texas
Fatmucket.
As with other freshwater mussel
species, the Texas pimpleback is also
threatened by impoundments. There are
37 major reservoirs and numerous
smaller impoundments within the
historical and current range of the Texas
pimpleback. There are 31 major
reservoirs within the Colorado River
basin, with another reservoir
(Goldthwaite Reservoir) proposed for
the Colorado River in San Saba County
near a Texas pimpleback population;
this reservoir was the number one
recommendation in the water plan for
the region (TWDB 2011, pp. 4–85).
There are 29 reservoirs within the
Guadalupe River basin and 34 within
the San Antonio River basin, each with
a storage capacity of 3,000 acre-feet or
more, and many other smaller reservoirs
(Exelon 2010, p. 2.3–4). The majority of
the large dams were constructed for
power generation, flood control, and
water supply by the Lower Colorado
River and Guadalupe-Blanco River
Authorities beginning as early as 1935
(Guadalupe-Blanco River Authority
2011, p. 1; LCRA 2011a, p. 1). These and
numerous smaller dams occur
throughout the Colorado and Guadalupe
River basins, fragmenting habitat and
populations of Texas pimpleback.
There are no natural lakes within the
range of the Texas pimpleback, nor has
it ever been found in reservoirs.
Historically, the Texas pimpleback
could be found in areas of the
Guadalupe River in Comal County
(Randklev et al. 2010c, p. 4), but it has
not been found in the area since the
construction of Canyon Reservoir
(Burlakova and Karatayev 2009, p. 6).
We presume the species is extirpated
from this reach because of the effects of
the reservoir. Surveys of other reservoirs
on the Guadalupe and Colorado Rivers
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have been ongoing since at least 1992,
and no evidence of live or dead Texas
pimpleback has been found in any
reservoir (Howells 1994, pp. 1–20; 1995,
pp. 1–50; 1996, pp. 1–45; 1997a, pp. 1–
58; 1998, pp. 1–30; 1999, pp. 1–34;
2000a, pp. 1–56; 2001, pp. 1–50; 2002a,
pp. 1–28; 2003, pp. 1–42; 2004, pp. 1–
48; 2005, pp. 1–23; 2006, pp. 1–106;
Karatayev and Burlakova 2008, pp. 1–
47; Burlakova and Karatayev 2010a, pp.
1–30; 2011, pp. 1–8), further indicating
that this species is not tolerant of
impoundments.
Texas pimpleback populations
downstream of dams are affected as
well. Cold water (less than 11 °C (52 °F))
has been shown to stunt mussel growth
(Hanson et al. 1988, p. 352) and reduce
or inhibit reproduction, because mussel
reproduction is temperature dependent
(Watters and O’Dee 1999, pp. 455).
Texas pimpleback living in cold-water
discharges downstream of large
impoundments are unlikely to
reproduce (Watters 2000, p. 264).
Dam construction also fragments the
range of Texas pimpleback, leaving
remaining habitats and populations
isolated by the structures as well as by
extensive areas of deep, uninhabitable,
impounded waters. These isolated
populations are unable to naturally
recolonize suitable habitat that may be
impacted by temporary but devastating
events, such as severe drought, chemical
spills, or unauthorized discharges. Dams
impound river habitats throughout
almost the entire range of the species.
These impoundments have left short
and isolated patches of suitable habitat,
typically in between impounded
reaches.
The widespread construction of dams
throughout the range of Texas
pimpleback has significantly altered
stream habitat both upstream and
downstream of the dams by changing
fish assemblages, temperature, dissolved
oxygen, and substrate. The effects of
dams are ongoing decades after
construction. Because of this loss of
habitat and its effects on the
populations, we conclude that the
effects of dams are a threat to the Texas
pimpleback.
Sedimentation
For general information on the effects
of sedimentation on freshwater mussels,
please refer to ‘‘Sedimentation’’ in
Factor A under Five-Factor Evaluation
for Texas Fatmucket.
As with other freshwater mussel
species, the Texas pimpleback is
affected by sedimentation. The
dominant land use in the Colorado
River basin is grazing (Hersh 2007, p.
11); soil compaction from intensive
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grazing may reduce infiltration rates and
increase runoff, and trampling of
riparian vegetation increases the
probability of erosion (Armour et al.
1994, p. 10; Brim Box and Mossa 1999,
p. 103). Even in 1959, the Guadalupe
River was noted as having high
sedimentation rates from agricultural
activities (Soil Conservation Service
1959, p. 59). Turbidity has also been
recorded as high in the Guadalupe River
near Victoria (Exelon 2010, p. 2.3–186),
indicating a large amount of suspended
sediment where a small Texas
pimpleback population was recently
found.
Streams occupied by Texas
pimpleback are subject to increasing
levels of sedimentation from agriculture,
urbanization, and sand and gravel
mining. Agriculture is a common land
use in the Guadalupe and San Antonio
River basins, and the city of San
Antonio, the second largest city in
Texas, continues to grow (City of San
Antonio 2010, p. 5). Sedimentation from
agriculture, urbanization, and sand and
gravel mining will continue to threaten
the Texas pimpleback in the foreseeable
future.
Dewatering
River dewatering can occur in several
ways: Anthropogenic activities such as
surface water diversions and
groundwater pumping, and natural
events, such as drought, which can
result in mussels stranded in previously
wetted areas. This is a particular
concern below reservoirs, whose water
levels are managed for various purposes
that can cause water levels in the
reservoir or downstream to rise or fall in
very short periods of time, such as when
hydropower facilities release water
during peak energy demand periods.
Drought can also severely impact
Texas pimpleback populations. Central
Texas, including the Colorado and
Guadalupe River basins, experienced a
major drought in the late 1970s (Lewis
and Oliveria 1979, p. 243). Near record
dry conditions in 2008 followed by a
pattern of below-normal rainfall during
the winter and spring of 2009 led to one
of the worst droughts in recorded
history for most of central Texas,
including the range of the Texas
pimpleback (Nielsen-Gammon and
McRoberts 2009, p. 2). This drought’s
severity was exacerbated by abnormally
high air temperatures, a likely effect of
climate change, which has already
increased average air temperatures in
Texas by at least 1 °C (1.8 °F) (NielsenGammon and McRoberts 2009, p. 22).
Instream flows throughout the Colorado
River basin during this drought were
significantly reduced (USGS 2011c, p. 1)
and Texas pimpleback populations in
areas with reduced water levels may
have been negatively affected. Central
Texas is currently experiencing another
extreme drought, with rainfall between
October 2010 and July 2011 being the
lowest on record during those months
(LCRA 2011c, p. 1); the effects of this
drought are being observed but are not
yet fully known. Droughts result in a
decrease in water depth and flow
velocity, which reduces food and
oxygen delivery. As droughts persist,
mussels face hypoxia, elevated water
temperature and, ultimately, stranding
(Golladay et al. 2004, p. 501).
We do not know the extent of the
impacts of stream dewatering on the
Texas pimpleback; however, because
several populations are small and
isolated, the loss of numerous
individuals at a site can have dramatic
consequences to the population.
Hydropower facilities, diversions
associated with construction, and
drought are occurring throughout the
range of the Texas pimpleback;
therefore, the effects of dewatering are
ongoing and unlikely to decrease,
resulting in significant threats to the
Texas pimpleback.
Sand and Gravel Mining
For general information on the effects
of sand and gravel mining on freshwater
mussels, please refer to ‘‘Sand and
Gravel Mining’’ in Factor A under FiveFactor Evaluation for Texas Fatmucket.
In 1995, the reach of the Guadalupe
River near Victoria, which contains a
Texas pimpleback population, was
described as having numerous current
and abandoned sand and gravel mining
areas (USACE 1995, p. 7). Currently,
TPWD has permitted one sand mining
activity within the current range of
Texas pimpleback, in the Guadalupe
River basin in Comal County (TPWD
2009b, p. 1); a small Texas pimpleback
population occurs downstream of this
area in the Guadalupe River. The permit
allows for the repeated removal of sand
and gravel at various locations within
the stream.
Headcuts from sand and gravel
mining operations have been
documented in the San Antonio River
basin in Karnes County from as early as
1967, with downstream channels having
steep, eroded banks (Kennon et al. 1967,
p. 22). There has been no evidence of
Texas pimpleback in Karnes County in
recent years (Howells 1997a, pp. 41–42),
and the effects of sand mining may have
been a factor in the species’ extirpation.
The Texas pimpleback population in
the Guadalupe River may be currently
threatened by sand and gravel mining.
These activities occur over a long period
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of time, destabilizing habitat both
upstream and downstream, which
decreases the likelihood of
recolonization after the activity has been
completed. Therefore, the effects of sand
and gravel mining are an ongoing threat
to the Texas pimpleback.
Chemical Contaminants
For general information on the effects
of chemical contaminants on freshwater
mussels, please refer to ‘‘Chemical
Contaminants’’ in Factor A under FiveFactor Evaluation for Texas Fatmucket.
As with other freshwater mussels, the
Texas pimpleback is affected by
chemical contaminants. TCEQ data for
2010 indicated that 26 of the 98
assessed water bodies within the
historical and current range of the Texas
pimpleback did not meet surface water
quality standards and were classified as
impaired water bodies under the Clean
Water Act (Texas Clean Rivers Program
2010a, p. 5). These water bodies were
impaired with dissolved solids, nitrates,
bacteria, low dissolved oxygen,
aluminum, sulfates, selenium, chloride,
and low pH associated with agricultural,
urban, municipal, and industrial runoff.
Additionally, the Concho River near
Paint Rock has been repeatedly
documented as having high nitrates
(Texas Clean Rivers Program 2008, p. 2);
a significant Texas pimpleback
population occurs just upstream of this
site. Nitrates and low dissolved oxygen
pose the greatest threat to Texas
pimpleback.
Within the range of Texas
pimpleback, several streams have been
listed as impaired due to high ammonia
concentrations, including Elm Creek in
the Guadalupe River basin (TCEQ
2010a, p. 294). Additionally, high
copper concentrations have been
recorded in the lower Guadalupe and
San Antonio Rivers (Lee and Schultz
1994, p. 8), and mercury has been
documented throughout the Guadalupe
and San Antonio Rivers, with
particularly high concentrations in fish
in the upper reaches of both rivers (Lee
and Schultz 1994, p. 8). Agricultural
pesticides and emerging contaminants
are likely also present in streams
inhabited by Texas pimpleback.
Chemical contaminants, such as
ammonia, copper, mercury, nutrients,
pesticides, and other compounds are
currently a threat to the Texas
pimpleback. The species is vulnerable
to acute contamination from spills as
well as chronic contaminant exposure,
which is occurring rangewide.
Summary of Factor A
The reduction in numbers and range
of the Texas pimpleback is primarily the
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result of the long-lasting effects of
habitat alterations such as the effects of
impoundments, sedimentation, sand
and gravel mining, and chemical
contaminants. Impoundments occur
throughout the range of the species and
have far-reaching effects both up and
downstream. Both the Colorado and
Guadalupe River systems have
experienced a large amount of
sedimentation from agriculture,
instream mining, and urban
development. Sand and gravel mining
affects Texas pimpleback habitat by
increasing sedimentation and channel
instability downstream and causing
headcutting upstream. Chemical
contaminants have been documented
throughout the range of the species and
may represent a significant threat to the
Texas pimpleback. Based upon our
review of the best commercial and
scientific data available, we conclude
that the present or threatened
destruction, modification, or
curtailment of its habitat or range is an
immediate threat of high magnitude to
the Texas pimpleback.
Factor B. Overutilization for
Commercial, Recreational, Scientific, or
Educational Purposes.
The Texas pimpleback was
historically harvested occasionally but
never experienced high levels of
collecting pressure (Howells 2010e,
p.10). Although levels were light
enough that commercial harvest was
likely not a threat to populations, all
commercial collecting became illegal
when Texas pimpleback was listed as
threatened by TPWD; therefore,
commercial harvest is not a current
threat to Texas pimpleback. Some
scientific collecting occurs but is not
likely to be a significant threat to the
species because it occurs only rarely.
However, handling mussels can disturb
gravid females and result in glochidial
loss and subsequent reproductive
failure. Additionally, handling has been
shown to reduce shell growth across
mussel species, including several
species of Lampsilis (Haag and
Commens-Carson 2008, pp. 505–506).
Repeated handling by researchers may
adversely affect Texas pimpleback
individuals, but these activities are
occurring rarely and are not likely to be
a threat to populations. Handling for
scientific purposes contributes to the
long-term conservation of the species.
We do not have any evidence of risks
to the Texas pimpleback from
overutilization for commercial,
recreational, scientific, or educational
purposes, and we have no reason to
believe this factor will become a threat
to the species in the future. Based upon
the best scientific and commercial
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information available, we conclude that
overutilization for commercial,
recreational, scientific, or educational
purposes does not pose a significant
threat to the Texas pimpleback
rangewide.
Factor C. Disease and Predation.
information on the effects of State and
Federal laws on the threats to freshwater
mussels in central Texas, please refer to
Factor D under Five-Factor Evaluation
for Texas
Disease
Little is known about disease in
freshwater mussels. However, disease is
believed to be a contributing factor in
documented mussel die-offs in other
parts of the United States (Neves 1987,
pp. 11–12). Diseases have not been
documented or observed during any
studies of Texas pimpleback.
Summary of Factor D
Predation
Raccoons will prey on freshwater
mussels stranded by low waters or
deposited in shallow water or on bars
following flooding or low water periods
(Howells 2010c, p. 12). Predation of
Texas pimpleback by raccoons may be
occurring occasionally but there is no
indication it is a significant threat to the
status of the species.
Some species of fish feed on mussels,
such as common carp, freshwater drum,
and redear sunfish, all of which are
common throughout the range of Texas
pimpleback (Hubbs et al. 2008, pp. 19,
45, 53). Common species of flatworms
are voracious predators of newly
metamorphosed juvenile mussels of
many species (Zimmerman et al. 2003,
p. 30). Predation is a normal factor
influencing the population dynamics of
a healthy mussel population; however,
predation may amplify declines in small
populations primarily caused by other
factors.
Summary of Factor C
Disease in freshwater mussels is
poorly known, and we do not have any
information indicating it is a threat to
the Texas pimpleback. Additionally,
predation is a natural ecological
interaction and we have no information
indicating the extent of any predation is
a threat to populations of Texas
pimpleback. Based upon the best
scientific and commercial information
available, we conclude that disease or
predation is not a threat to the Texas
pimpleback.
Factor D. The Inadequacy of Existing
Regulatory Mechanisms.
Existing regulatory mechanisms that
could have an effect on threats to the
Texas pimpleback include State and
Federal laws such as Texas Threatened
and Endangered Species regulations and
freshwater mussel sanctuaries, State and
Federal sand and gravel mining
regulations, and regulation of point and
non-point source pollution. For more
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Fatmucket
Despite State and Federal laws
protecting the species and water quality,
the Texas pimpleback continues to
decline due to the effects of habitat
destruction, poor water quality,
contaminants, and other factors. The
regulatory measures described above
have been insufficient to significantly
reduce or remove the threats to the
Texas pimpleback. Based upon our
review of the best commercial and
scientific data available, we conclude
that the lack of existing regulatory
mechanisms is an immediate threat of
moderate magnitude to the Texas
pimpleback.
Factor E. Other Natural or Manmade
Factors Affecting Its Continued
Existence.
Natural and manmade factors that
threaten the Texas pimpleback include
climate change, population
fragmentation and isolation, and
nonnative species.
Climate Change
For general information on the effects
of climate change on freshwater mussels
of central Texas, please refer to‘‘Climate
Change’’ in Factor E under Five-Factor
Evaluation for Texas Fatmucket.
Because the range of the Texas
pimpleback has been reduced to
isolated locations with low population
numbers in small rivers and streams, the
Texas pimpleback is vulnerable to
climatic changes that could decrease the
availability of water.
The disjunct nature of the remaining
Texas pimpleback populations, coupled
with the limited ability of mussels to
migrate, makes it unlikely that Texas
pimpleback can adjust their range in
response to changes in climate (Strayer
2008, p. 30). Climate change could affect
the Texas pimpleback through the
combined effects of global and regional
climate change, along with the
increased probability of long-term
drought. Climate change exacerbates
threats such as habitat degradation from
prolonged periods of drought, increased
water temperature, and the increased
allocation of water for municipal,
agricultural, and industrial use. Climate
change may be a significant stressor that
exacerbates existing threats by
increasing the likelihood of prolonged
drought. As such, climate change, in
and of itself, may affect the Texas
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pimpleback, but the magnitude and
imminence of the effects remain
uncertain. Based upon our review of the
best commercial and scientific data
available, we conclude that the effects of
climate change in the future will likely
exacerbate the current and ongoing
threats of habitat loss and degradation
caused by other factors, as discussed
above.
Population Fragmentation and Isolation
For more information on the effects of
population fragmentation and isolation
on freshwater mussels of central Texas,
please refer to ‘‘Population
Fragmentation and Isolation’’ in Factor
E under Five-Factor Evaluation for
Texas Fatmucket. As with many
freshwater mussels, most of the
remaining populations of the Texas
pimpleback are small and
geographically isolated and thus are
susceptible to genetic drift, inbreeding
depression, and random or chance
changes to the environment, such as
toxic chemical spills (Watters and Dunn
1995, pp. 257–258) or dewatering.
Historically, the Texas pimpleback was
once widespread throughout much of
the Colorado and Guadalupe River
systems when few natural barriers
existed to prevent migration (via host
species) among suitable habitats. The
extensive impoundment of the Colorado
and Guadalupe River basins has
fragmented Texas pimpleback
populations throughout these river
systems.
Small Texas pimpleback populations,
including those in the lower Guadalupe
River, mainstem Colorado River, and
San Marcos River, may be below the
minimum population size required to
maintain population viability into the
future. These populations are more
vulnerable to extirpation since they are
less likely to be able to recover through
recruitment from events that reduce but
do not extirpate populations.
Additionally, these small populations
are more vulnerable to extirpation from
stochastic events, as the lack of
connectivity among populations does
not permit nearby populations to
recolonize areas affected by intense
droughts, toxic spills, or other isolated
events that result in significant mussel
die-offs. While the small, isolated
populations do not represent an
independent threat to the species, the
situation does substantially increase the
risk of extirpation from the effects of all
other threats, including those addressed
in this analysis, and those that could
occur in the future from unknown
sources.
Based upon our review of the best
commercial and scientific data
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available, we conclude that
fragmentation and isolation of small
remaining populations of the Texas
pimpleback are occurring and are
ongoing threats to the species
throughout all of its range. Further,
stochastic events may play a magnified
role in extirpation of small, isolated
populations.
Nonnative Species
For general information on the effects
of nonnative species on freshwater
mussels of central Texas, please refer to
‘‘Nonnative Species’’ in Factor E under
Five-Factor Evaluation for Texas
Fatmucket. As with other freshwater
mussels, the Texas pimpleback is
threatened by nonnative species.
Various nonnative aquatic species pose
a threat to the Texas pimpleback,
including golden algae, zebra mussels,
and black carp. Of these, golden algae
has been responsible for killing more
than two million fish in the Colorado
River since 1989 (TPWD 2010a, p. 1).
Although mussel kills due to golden
algae have not been recorded, we expect
golden algae to negatively affect mussel
populations through loss of host fish
and direct toxicity. Zebra mussels and
black carp do not currently occur within
the range of the Texas pimpleback,
although both are found in Texas and
could be introduced to the Colorado and
Guadalupe Rivers in the forseeable
future. Their introduction into the range
of Texas pimpleback would be
devastating.
Based upon our review of the best
commercial and scientific data
available, we conclude that golden algae
is an ongoing threat to the Texas
pimpleback and other nonnative
species, such as zebra mussels and black
carp, are a potential threat to the Texas
pimpleback that is likely to increase as
these exotic species expand their
occupancy within the range of the Texas
pimpleback.
Summary of Factor E
The effects of climate change, while
difficult to quantify at this time, are
likely to exacerbate the current and
ongoing threat of habitat loss caused by
other factors, and the small sizes and
fragmented nature of the remaining
populations render them more
vulnerable to extirpation. In addition,
nonnative species, such as golden algae,
currently threaten the Texas fatmucket,
and the potential introduction of zebra
mussels and black carp are potential
future threats. Based upon our review of
the best commercial and scientific data
available, we conclude that other
natural or manmade factors are
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immediate threats of moderate
magnitude to the Texas pimpleback.
Finding for Texas Pimpleback
As required by the Act, we considered
the five factors in assessing whether the
Texas pimpleback is threatened or
endangered throughout all of its range.
We examined the best scientific and
commercial information available
regarding the past, present, and future
threats faced by the Texas pimpleback.
We reviewed the petition, information
available in our files, and other
available published and unpublished
information, and we consulted with
recognized Texas pimpleback experts
and other Federal and State agencies.
This status review identifies threats to
the Texas pimpleback attributable to
Factors A, D, and E. The primary threat
to the species is from habitat destruction
and modification (Factor A) from
impoundments, which scour riverbeds,
thereby removing mussel habitat,
decrease water quality, modify stream
flows, and restrict fish host migration
and distribution of freshwater mussels.
Additional threats under Factor A
include sedimentation, dewatering,
sand and gravel mining, and chemical
contaminants. Also, most of these
threats may be exacerbated by the
current and projected effects of climate
change (discussed under Factor E).
Threats to the Texas pimpleback are not
being adequately addressed through
existing regulatory mechanisms (Factor
D). Because of the limited distribution
of this endemic species and its lack of
mobility, these threats are likely to lead
to the extinction of the Texas
pimpleback in the foreseeable future.
On the basis of the best scientific and
commercial information available, we
find that the petitioned action to list the
Texas pimpleback under the Act is
warranted. We will make a
determination on the status of the
species as threatened or endangered
when we complete a proposed listing
determination. When we complete a
proposed listing determination, we will
examine whether the species may be
endangered or threatened throughout all
of its range or whether the species may
be endangered or threatened in a
significant portion of its range.
However, as explained in more detail
below, an immediate proposal of a
regulation implementing this action is
precluded by higher priority listing
actions, and progress is being made to
add or remove qualified species from
the Lists of Endangered and Threatened
Wildlife and Plants.
We reviewed the available
information to determine if the existing
and foreseeable threats render the Texas
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pimpleback at risk of extinction now
such that issuing an emergency
regulation temporarily listing the
species under section 4(b)(7) of the Act
is warranted. We determined that
issuing an emergency regulation
temporarily listing the species is not
warranted for the Texas pimpleback at
this time, because we have not
identified a threat or activity that poses
a significant risk, such that losses to the
species during the normal listing
process would endanger the continued
existence of the entire species. However,
if at any time we determine that issuing
an emergency regulation temporarily
listing the Texas pimpleback is
warranted, we will initiate this action at
that time.
Listing Priority Number for Texas
Pimpleback
The Service adopted guidelines on
September 21, 1983 (48 FR 43098), to
establish a rational system for utilizing
available resources for the highest
priority species when adding species to
the Lists of Endangered and Threatened
Wildlife and Plants or reclassifying
species listed as threatened to
endangered status. These guidelines,
titled ‘‘Endangered and Threatened
Species Listing and Recovery Priority
Guidelines’’ address the immediacy and
magnitude of threats, and the level of
taxonomic distinctiveness by assigning
priority in descending order to
monotypic genera (genus with one
species), full species, and subspecies (or
equivalently, distinct population
segments of vertebrates).
As a result of our analysis of the best
available scientific and commercial
information, we have assigned the Texas
pimpleback an LPN of 2, based on our
finding that the species faces threats
that are of high magnitude and are
imminent. These threats include habitat
loss and degradation from
impoundments, sedimentation, sand
and gravel mining, and chemical
contaminants; other natural or
manmade factors such as climate
change, small, isolated populations, and
nonnative species; and the fact that the
threats to the species are not being
adequately addressed by existing
regulatory mechanisms. Our rationale
for assigning the Texas pimpleback an
LPN of 2 is outlined below.
We consider the threats that the Texas
pimpleback faces to be high in
magnitude. Habitat loss and degradation
from impoundments, sedimentation,
sand and gravel mining, and chemical
contaminants are widespread
throughout the range of the Texas
pimpleback and profoundly affect its
habitat, and remaining populations are
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small, isolated, and highly vulnerable to
stochastic events.
Under our LPN guidelines, the second
criterion we consider in assigning a
listing priority is the immediacy of
threats. We consider the threats to the
Texas pimpleback as described under
Factors A, D, and E in the Five-Factor
Evaluation for Texas Pimpleback
section to be imminent because these
threats are ongoing and will continue in
the foreseeable future. Habitat loss and
destruction has already occurred and
will continue as the human population
continues to grow in central Texas. The
Texas pimpleback populations may
already be below the minimum viable
population requirement, which would
cause a reduction in the number of
populations and an increase in the
species’ vulnerability to extinction.
These threats are exacerbated by climate
change, which will increase the
frequency and magnitude of droughts.
Therefore, we consider these threats to
be imminent.
Thirdly, the Texas pimpleback is a
valid taxon at the species level and,
therefore, receives a higher priority than
subspecies, but a lower priority than
species in a monotypic genus.
Therefore, we assigned Texas
pimpleback an LPN of 2. We will
continue to monitor the threats to the
Texas pimpleback and the species’
status on an annual basis, and should
the magnitude or imminence of the
threats change, we will revisit our
assessment of the LPN.
While we conclude that listing the
Texas pimpleback is warranted, an
immediate proposal to list this species
is precluded by other higher priority
listings, which we address in the
Preclusion and Expeditious Progress
section below. Because we have
assigned the Texas pimpleback an LPN
of 2, work on a proposed listing
determination for the species is
precluded by work on higher priority
listing actions with absolute statutory,
court-ordered, or court-approved
deadlines and final listing
determinations for those species that
were proposed for listing with funds
from Fiscal Year (FY) 2010. This work
includes all the actions listed in the
tables below under Preclusion and
Expeditious Progress.
Five-Factor Evaluation for Texas
Fawnsfoot
Information pertaining to the Texas
fawnsfoot in relation to the five factors
provided in section 4(a)(1) of the Act is
discussed below.
Factor A. The Present or Threatened
Destruction, Modification, or
Curtailment of Its Habitat or Range.
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As discussed above, the decline of
mussels in Texas and across the United
States is primarily the result of habitat
loss and degradation. Chief among the
causes of decline of the Texas fawnsfoot
in Texas are the effects of
impoundments, sedimentation,
dewatering, sand and gravel mining,
and chemical contaminants. These
threats are discussed below.
Impoundments
For general information on the effects
of impoundments on freshwater
mussels, please refer to
‘‘Impoundments’’ in Factor A under
Five-Factor Evaluation for Texas
Fatmucket. Impoundments and
numerous smaller dams occur
throughout the Colorado and Guadalupe
River basins, fragmenting habitat and
populations of Texas fawnsfoot. There
are 74 major reservoirs and numerous
smaller impoundments within the
historical and current range of the
smooth pimpleback. Thirty-one of the
74 major reservoirs are located within
the Colorado River basin and the
remaining 43 reservoirs are located
within the Brazos River basin. There are
also eleven new reservoirs that have
been recommended for development as
feasible alternatives to meet future water
needs within the Brazos River basin
(Brazos G Regional Water Planning
Group 2010, p. 4B.12–1). In addition,
six new off-channel reservoirs are also
being considered for future
development (Brazos G Regional Water
Planning Group 2010, p. 4B.13–2).
There are no natural lakes within the
range of the Texas fawnsfoot, nor has it
ever been found in reservoirs. Surveys
of the reservoirs on the Brazos and
Colorado Rivers have been ongoing
since at least 1992, and no evidence of
live or dead Texas pimpleback has been
found in any reservoir (Howells 1994,
pp. 1–20; 1995, pp. 1–50; 1996, pp. 1–
45; 1997a, pp. 1–58; 1998, pp. 1–30;
1999, pp. 1–34; 2000a, pp. 1–56; 2001,
pp. 1–50; 2002a, pp. 1–28; 2003, pp. 1–
42; 2004, pp. 1–48; 2005, pp. 1–23;
2006, pp. 1–106; Karatayev and
Burlakova 2008, pp. 1–47; Burlakova
and Karatayev 2010a, pp. 1–30; 2011,
pp. 1–8), further indicating that this
species is not tolerant of
impoundments.
Texas fawnsfoot populations
downstream of dams are affected as
well. Cold water (less than 11 °C (52 °F))
has been shown to stunt mussel growth
(Hanson et al. 1988, p. 352) and reduce
or inhibit reproduction, because mussel
reproduction is temperature dependent
(Watters and O’Dee 1999, pp. 455).
Texas fawnsfoot living in cold-water
discharges downstream of large
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impoundments are unlikely to
reproduce (Watters 2000, p. 264).
Dam construction also fragments the
range of Texas fawnsfoot, leaving
remaining habitats and populations
isolated by the structures as well as by
extensive areas of deep, uninhabitable,
impounded waters. These isolated
populations are unable to naturally
recolonize suitable habitat that may be
impacted by temporary but devastating
events, such as severe drought, chemical
spills, or unauthorized discharges. Dams
impound river habitats throughout
almost the entire range of the species.
These impoundments have left short
and isolated patches of remnant habitat,
typically in between impounded
reaches. Habitat downstream of dams
may be impaired for many miles; in the
Brazos River downstream of Possum
Kingdom Reservoir, substrate was
unstable for 150 km (240 mi) below the
dam (Yeager 1993, p. 68).
The widespread construction of dams
throughout the range of Texas fawnsfoot
has significantly altered stream habitat
both upstream and downstream of the
dams by changing fish assemblages,
temperature, dissolved oxygen, and
substrate. The effects of dams are
ongoing decades after construction.
Because of this loss of habitat and its
effects on the populations, we conclude
that the effects of dams are a threat to
the Texas fawnsfoot.
Sedimentation
For general information on the effects
of sedimentation on freshwater mussels,
please refer to ‘‘Sedimentation’’ in
Factor A under Five-Factor Evaluation
for Texas Fatmucket.
As with other freshwater mussel
species, the Texas fawnsfoot is also
threatened by sedimentation. The
dominant land use in the Colorado
River basin is grazing (Hersh 2007, p.
11); soil compaction from intensive
grazing may reduce infiltration rates and
increase runoff, and trampling of
riparian vegetation increases the
probability of erosion (Armour et al.
1994, p. 10; Brim Box and Mossa 1999,
p. 103). Additionally, much of the
Brazos River basin is grazed or farmed
for row crops, which can contribute
large amounts of sediment to the basin
(Brazos River Authority 2007, p. 4).
Reservoir construction in the upper
portion of the basin has been attributed
with the erosion and subsequent
sedimentation of the lower river (USGS
2001, p. 30), as sediment-poor tailwaters
scour the riverbanks below the dam and
deposit sediment farther downstream. In
2004, sedimentation was high enough in
the Brazos River below Possum
Kingdom Reservoir to cause residents to
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raise concerns to the Brazos River
Authority (Brazos River Authority 2006,
p. 2). Elevated suspended sediment
levels have been reported throughout
the basin (Brazos River Authority 2006,
p. 8).
The LCRA TSC is proposing to
construct two new 345-kV electric
transmission line facilities between Tom
Green (in the Colorado River basin near
San Angelo) and Kendall Counties (in
the Guadalupe River basin north of San
Antonio) to provide electrical power to
accommodate increased demand (Clary
2010, p. 1). One of the proposed project
lines would cross the San Saba River,
which contains one of the more
numerous Texas fawnsfoot populations.
The proposed project could negatively
affect Texas fawnsfoot habitat by
clearing land within the riparian zone
and may increase sediment runoff into
the San Saba River (Clary 2010, p. 9).
Similar activities to accommodate Texas
population growth and demands are
expected to be undertaken across the
species’ range and will likely lead to
additional sources of sediment in the
streams inhabited by the Texas
fawnsfoot.
The City of Austin lies within the
Colorado River basin, and 3.9 million
people live within the Brazos River
basin (Brazos River Authority 2007, p.
1). The range of the Texas fawnsfoot
receives sediment from agriculture,
urbanization, and sand and gravel
mining. Sedimentation will continue to
threaten the Texas fawnsfoot in the
foreseeable future.
Dewatering
River dewatering can occur in several
ways: anthropogenic activities such as
surface water diversions and
groundwater pumping, and natural
events, such as drought, which can
result in mussels stranded in previously
wetted areas. This is a particular
concern below reservoirs, whose water
levels are managed for various purposes
that can cause water levels in the
reservoir or downstream to rise or fall in
very short periods of time, such as when
hydropower facilities release water
during peak energy demand periods.
Drought can also severely impact
Texas fawnsfoot populations. Central
Texas, including the Colorado and
Brazos River basins, experienced a
major drought in the late 1970s (Lewis
and Oliveria 1979, p. 243). Near record
dry conditions in 2008 followed by a
pattern of below-normal rainfall during
the winter and spring of 2009 led to one
of the worst droughts in recorded
history for most of central Texas,
including the range of the Texas
fawnsfoot (Nielsen-Gammon and
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McRoberts 2009, p. 2). This drought’s
severity was exacerbated by abnormally
high air temperatures, a likely effect of
climate change, which has already
increased average air temperatures in
Texas by at least 1 °C (1.8 °F) (NielsenGammon and McRoberts 2009, p. 22).
Instream flows throughout the Colorado
River basin during this drought were
significantly reduced (USGS 2011c, p.
1), and Texas fawnsfoot populations in
areas with reduced water levels may
have been negatively affected. Central
Texas is currently experiencing another
extreme drought, with rainfall between
October 2010 and July 2011 being the
lowest on record during those months
(LCRA 2011c, p. 1); the effects of this
drought are being observed but are not
yet fully known. Droughts result in a
decrease in water depth and flow
velocity, which reduces food and
oxygen delivery. As droughts persist,
mussels face hypoxia, elevated water
temperature and, ultimately, stranding
(Golladay et al. 2004, p. 501).
We do not know the extent of the
impacts of stream dewatering on the
Texas fawnsfoot; however, because
several populations are small and
isolated, the loss of numerous
individuals at a site can have dramatic
consequences to the population.
Hydropower facilities, construction, and
drought are occurring throughout the
range of the Texas fawnsfoot; therefore,
the effects of dewatering are ongoing
and unlikely to decrease, resulting in
significant threats to the Texas
fawnsfoot.
Sand and Gravel Mining
For general information on the effects
of sand and gravel mining on freshwater
mussels, please refer to ‘‘Sand and
Gravel Mining’’ in Factor A under FiveFactor Evaluation for Texas Fatmucket.
The Brazos River has a long history of
sand mining, particularly in the lower
river, and channel morphology changes
have been attributed to destabilization
due to instream sand mining in the area
(USGS 2001, p. 27). The removal of sand
from within the river creates sediment
traps during periods of high flow, which
causes scouring and erosion
downstream (USGS 2001, p. 27). A
gravel dredging operation in the Brazos
River has been documented as
depositing sediment as far as 1.6 km (1
mile) downstream (Forshage and Carter
1973, p. 697). Accelerated stream bank
erosion and downcutting of streambeds
are common effects of instream sand
and gravel mining, as is the
mobilization of fine sediments during
sand and gravel extraction (Roell 1999,
p. 7).
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Within the current range of Texas
fawnsfoot, TPWD has issued permits for
four sand mining activities in the Brazos
River basin (Austin, Bosque, and Fort
Bend Counties) (TPWD 2004, p. 1;
2007b, p. 1; 2008b, p. 1; 2010b, p. 1). All
of the permits allow for the repeated
removal of sand and gravel at various
locations within a stream. The lower
Brazos River, near where these mining
activities are occurring, contains a small
Texas fawnsfoot population.
The Texas fawnsfoot population in
the lower Brazos River is likely
threatened by sand and gravel mining.
These activities occur over a long period
of time, destabilizing habitat both
upstream and downstream, which
decreases the likelihood of
recolonization after the activity has been
completed. Therefore, the effects of sand
and gravel mining are an ongoing threat
to the Texas fawnsfoot.
Chemical Contaminants
For general information on the effects
of chemical contaminants on freshwater
mussels, please refer to ‘‘Chemical
Contaminants’’ under Factor A under
Five-Factor Evaluation for Texas
Fatmucket.
As with other freshwater mussels, the
Texas fawnsfoot is also affected by
chemical contaminants. TCEQ data for
2010 indicated that 26 of the 98
assessed water bodies within Colorado
River basin and 81 of approximately 124
assessed water bodies within Brazos
River basin did not meet surface water
quality standards and were classified as
303(d) impaired Water Bodies (Texas
Clean Rivers Program 2010a, p. 5; TCEQ
2010c, pp. 1–106). These water bodies
were impaired with dissolved solids,
nitrites, nitrates, bacteria, low dissolved
oxygen, aluminum, sulfates, selenium,
chloride, orthophosphorus, phosphorus,
Chlorophyll a, and low pH associated
with agricultural, urban, municipal, and
industrial runoff. Of these, nitrates and
low dissolved oxygen pose a threat to
Texas fawnsfoot, as discussed above.
In 2010, crude oil overflowed into
Keechi Creek in Leon County, a
tributary to Navasota River (National
Response Center 2010, p. 2). This
location is upstream of one of the few
remaining Texas fawnsfoot populations.
Numerous other spills have occurred
within the range of the Texas fawnsfoot.
These can occur from on site accidents
(tank, pipeline spills) or from tanker
truck accidents within watersheds
occupied by Texas fawnsfoot. For
example, oil has spilled into the Brazos
River a number of times. As much as
320,000 L (84,000 gal) of crude oil was
spilled in the Brazos River in 1991
(Associated Press 1991, p. 1). In June
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2010, flooding of holding ponds
adjacent to oil drilling operations leaked
oil into Thompson Creek and
subsequently into the Brazos River.
Also, in July 2010, oil pipelines burst
and released approximately 165 barrels
of crude oil into the upper Brazos River
(Joiner 2010, p. 1).
Agricultural pesticides and emerging
contaminants are likely also present in
streams inhabited by Texas fawnsfoot.
There are 53 wastewater treatment
plants permitted to discharge into the
Brazos River basin (Valenti and Brooks
2008, p. 12); the outfalls from these
treatment plants have not been tested to
determine if they contain contaminants
of note.
Chemical contaminants, such as oil,
ammonia, copper, mercury, nutrients,
pesticides, and other compounds are
currently a threat to the Texas
fawnsfoot. The species is vulnerable to
acute contamination from spills as well
as chronic contaminant exposure, which
is occurring rangewide.
Summary of Factor A
The reduction in numbers and range
of the Texas fawnsfoot is primarily the
result of the long-lasting effects of
habitat alterations such as the effects of
impoundments, sedimentation, sand
and gravel mining, and chemical
contaminants. Impoundments occur
throughout the range of the species and
have far-reaching effects both up- and
downstream. Both the Colorado and
Brazos River systems have experienced
a large amount of sedimentation from
agriculture, sand and gravel mining, and
urban development. Sand and gravel
mining affects Texas fawnsfoot habitat
by increasing sedimentation and
channel instability downstream and
causing headcutting upstream. Chemical
contaminants have been documented
throughout the range of the species and
may represent a significant threat to the
Texas fawnsfoot. Based upon our review
of the best commercial and scientific
data available, we conclude that the
present or threatened destruction,
modification, or curtailment of its
habitat or range is an immediate and
ongoing threat of high magnitude to the
Texas fawnsfoot.
Factor B. Overutilization for
Commercial, Recreational, Scientific, or
Educational Purposes.
The Texas fawnsfoot is not a
commercially valuable species and has
never been harvested in Texas as a
commercial mussel species (Howells
2010d, pp. 9–10). Some scientific
collecting occurs but is not likely to be
a significant threat to the species
because it occurs only rarely. However,
handling mussels can disturb gravid
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females and result in glochidial loss and
subsequent reproductive failure.
Additionally, handling has been shown
to reduce shell growth across mussel
species, including several species of
Lampsilis (Haag and Commens-Carson
2008, pp. 505–506). Repeated handling
by researchers may adversely affect
Texas fawnsfoot individuals, but these
activities are occurring rarely and are
not likely to be a threat to populations.
Handling for scientific purposes
contributes to the long-term
conservation of the species.
We do not have any evidence of risks
to the Texas fawnsfoot from
overutilization for commercial,
recreational, scientific, or educational
purposes, and we have no reason to
believe this factor will become a threat
to the species in the future. Based upon
the best scientific and commercial
information available, we conclude that
overutilization for commercial,
recreational, scientific, or educational
purposes does not pose a significant
threat to the Texas fawnsfoot rangewide.
Factor C. Disease and Predation.
Disease
Little is known about disease in
freshwater mussels. However, disease is
believed to be a contributing factor in
documented mussel die-offs in other
parts of the United States (Neves 1987,
pp. 11–12). Diseases have not been
documented or observed during any
studies of Texas fawnsfoot.
Predation
Raccoons will prey on freshwater
mussels stranded by low waters or
deposited in shallow water or on bars
following flooding or low water periods
(Howells 2010c, p. 12). Predation of
Texas fawnsfoot by raccoons may be
occurring occasionally but there is no
indication it is a significant threat to the
status of the species.
Some species of fish feed on mussels,
such as common carp, freshwater drum,
and redear sunfish, all of which are
common throughout the range of Texas
fawnsfoot (Hubbs et al. 2008, pp. 19, 45,
53). Common species of flatworms are
voracious predators of newly
metamorphosed juvenile mussels of
many species (Zimmerman et al. 2003,
p. 30). Predation is a normal factor
influencing the population dynamics of
a healthy mussel population; however,
predation may amplify declines in small
populations primarily caused by other
factors.
Summary of Factor C
Disease in freshwater mussels is
poorly known, and we do not have any
information indicating it is a threat to
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the Texas fawnsfoot. Additionally,
predation is a natural ecological
interaction and we have no information
indicating the extent of any predation is
a threat to populations of Texas
fawnsfoot. Based upon the best
scientific and commercial information
available, we conclude that disease or
predation is not a threat to the Texas
fawnsfoot.
Factor D. The Inadequacy of Existing
Regulatory Mechanisms.
Existing regulatory mechanisms that
could have an effect on threats to the
Texas fawnsfoot include State and
Federal laws such as Texas Threatened
and Endangered Species regulations and
freshwater mussel sanctuaries, State and
Federal sand and gravel mining
regulations, and regulation of point and
non-point source pollution. For more
information on the effects of State and
Federal laws on the threats to freshwater
mussels in central Texas, please refer to
Factor D under Five-Factor Evaluation
for Texas Fatmucket.
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Summary of Factor D
Despite State and Federal laws
protecting the species and water quality,
the Texas fawnsfoot continues to
decline due to the effects of habitat
destruction, poor water quality,
contaminants, and other factors. The
regulatory measures described in Factor
D under Five-Factor Evaluation for
Texas Fatmucket have been insufficient
to significantly reduce or remove the
threats to the Texas fawnsfoot. Based
upon our review of the best commercial
and scientific data available, we
conclude that the lack of existing
regulatory mechanisms is an immediate
threat of moderate magnitude to the
Texas fawnsfoot.
Factor E. Other Natural or Manmade
Factors Affecting Its Continued
Existence.
Natural and manmade factors that
threaten the Texas fawnsfoot include
climate change, population
fragmentation and isolation, and
nonnative species.
Climate Change
For general information on the effects
of climate change on freshwater mussels
in central Texas, please refer to
‘‘Climate Change’’ in Factor E under
Five-Factor Evaluation for Texas
Fatmucket. Because the range of the
Texas fawnsfoot has been reduced to
isolated locations, many with low
population numbers, in small rivers and
streams, the Texas fawnsfoot is
vulnerable to climatic changes that
could decrease the availability of water.
The disjunct nature of the remaining
Texas fawnsfoot populations, coupled
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with the limited ability of mussels to
migrate, makes it unlikely that Texas
fawnsfoot can adjust their range in
response to changes in climate (Strayer
2008, p. 30). Climate change could affect
the Texas fawnsfoot through the
combined effects of global and regional
climate change, along with the
increased probability of long-term
drought. Climate change exacerbates
threats such as habitat degradation from
prolonged periods of drought, increased
water temperature, and the increased
allocation of water for municipal,
agricultural, and industrial use. Climate
change may be a significant stressor that
exacerbates existing threats by
increasing the likelihood of prolonged
drought. As such, climate change, in
and of itself, may affect the Texas
fawnsfoot, but the magnitude and
imminence of the effects remain
uncertain. Based upon our review of the
best commercial and scientific data
available, we conclude that the effects of
climate change in the future will likely
exacerbate the current and ongoing
threats of habitat loss and degradation
caused by other factors, as discussed
above.
Population Fragmentation and Isolation
For general information on the effects
of population fragmentation and
isolation on freshwater mussels in
central Texas, please refer to
‘‘Population Fragmentation and
Isolation’’ in Factor E under Five-Factor
Evaluation for Texas Fatmucket. As
with many freshwater mussels, most of
the remaining populations of the Texas
fawnsfoot are small and geographically
isolated and thus are susceptible to
genetic drift, inbreeding depression, and
random or chance changes to the
environment, such as toxic chemical
spills (Watters and Dunn 1995, pp. 257–
258) or dewatering. Historically, the
Texas fawnsfoot was once widespread
throughout much of the Colorado and
Brazos River systems when few natural
barriers existed to prevent migration
(via host species) among suitable
habitats. The extensive impoundment of
the Colorado and Brazos River basins
has fragmented Texas fawnsfoot
populations throughout these river
systems.
Small Texas fawnsfoot populations,
including those in the Brazos River,
Clear Fork Brazos River, Navasota River,
and Deer Creek, may be below the
minimum population size required to
maintain population viability into the
future. These populations are more
vulnerable to extirpation since they are
less likely to be able to recover through
recruitment from events that reduce but
do not extirpate populations.
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Additionally, these small populations
are more vulnerable to extirpation from
stochastic events, as the lack of
connectivity among populations does
not permit nearby populations to
recolonize areas affected by intense
droughts, toxic spills, or other isolated
events that result in significant mussel
dieoffs. While the small, isolated
populations do not represent an
independent threat to the species, the
situation does substantially increase the
risk of extirpation from the effects of all
other threats, including those addressed
in this analysis, and those that could
occur in the future from unknown
sources.
Based upon our review of the best
commercial and scientific data
available, we conclude that
fragmentation and isolation of small
remaining populations of the Texas
fawnsfoot are occurring and are ongoing
threats to the species throughout all of
its range; these threats will continue.
Further, stochastic events may play a
magnified role in extirpation of small,
isolated populations.
Nonnative Species
For general information on the effects
of nonnative species on freshwater
mussels in central Texas, please refer to
‘‘Nonnative Species’’ in Factor E under
Five-Factor Evaluation for Texas
Fatmucket. As with other freshwater
mussels, the Texas fawnsfoot is
threatened by nonnative species.
Various nonnative aquatic species pose
a threat to the Texas fawnsfoot,
including golden algae, zebra mussels,
and black carp. Of these, golden algae
has been responsible for killing more
than two million fish in the Colorado
River since 1989 (TPWD 2010a, p. 1).
Although mussel kills due to golden
algae have not been recorded, we expect
golden algae to negatively affect mussel
populations through loss of host fish
and direct toxicity. Zebra mussels and
black carp do not currently occur within
the range of the Texas fawnsfoot,
although both are found in Texas and
could be introduced to the Brazos and
Colorado Rivers in the future. Based on
population responses of other mussel
species that overlap with zebra mussels
and black carp in similar river
conditions, we conclude that the
introduction of zebra mussels or black
carp into the range of smooth
pimpleback would be devastating to the
species.
Based upon our review of the best
commercial and scientific data
available, we conclude that golden algae
is an ongoing threat to the Texas
fawnsfoot, and other nonnative species,
such as zebra mussels and black carp,
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are a potential threat to the Texas
fawnsfoot that is likely to increase as
these exotic species expand their
occupancy within the range of the Texas
fawnsfoot.
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Summary of Factor E
The effects of climate change, while
difficult to quantify at this time, are
likely to exacerbate the current and
ongoing threat of habitat loss caused by
other factors, and the small sizes and
fragmented nature of the remaining
populations render them more
vulnerable to extirpation. In addition,
nonnative species, such as golden algae,
currently threaten the Texas fatmucket,
and the potential introduction of zebra
mussels and black carp are potential
future threats. Based upon our review of
the best commercial and scientific data
available, we conclude that other
natural or manmade factors are
immediate threats of moderate
magnitude to the Texas fawnsfoot.
Finding for Texas Fawnsfoot
As required by the Act, we considered
the five factors in assessing whether the
Texas fawnsfoot is threatened or
endangered throughout all of its range.
We examined the best scientific and
commercial information available
regarding the past, present, and future
threats faced by the Texas fawnsfoot.
We reviewed the petition, information
available in our files, and other
available published and unpublished
information, and we consulted with
recognized Texas fawnsfoot experts and
other Federal and State agencies.
This status review identifies threats to
the Texas fawnsfoot attributable to
Factors A, D, and E. The primary threat
to the species is from habitat destruction
and modification (Factor A) from
impoundments, which scour riverbeds,
thereby removing mussel habitat,
decrease water quality, modify stream
flows, and restrict fish host migration
and distribution of freshwater mussels.
Additional threats under Factor A
include sedimentation, dewatering,
sand and gravel mining, and chemical
contaminants. Also, most of these
threats may be exacerbated by the
current and projected effects of climate
change (discussed under Factor E).
Threats to the Texas fawnsfoot are not
being adequately addressed through
existing regulatory mechanisms (Factor
D). Because of the limited distribution
of this endemic species and its lack of
mobility, these threats are likely to lead
to the extinction of the Texas fawnsfoot
in the foreseeable future.
On the basis of the best scientific and
commercial information available, we
find that the petitioned action to list the
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Texas fawnsfoot under the Act is
warranted. We will make a
determination on the status of the
species as threatened or endangered
when we complete a proposed listing
determination. When we complete a
proposed listing determination, we will
examine whether the species may be
endangered or threatened throughout all
of its range or whether the species may
be endangered or threatened in a
significant portion of its range.
However, as explained in more detail
below, an immediate proposal of a
regulation implementing this action is
precluded by higher priority listing
actions, and progress is being made to
add or remove qualified species from
the Lists of Endangered and Threatened
Wildlife and Plants.
We reviewed the available
information to determine if the existing
and foreseeable threats render the Texas
fawnsfoot at risk of extinction now such
that issuing an emergency regulation
temporarily listing the species under
section 4(b)(7) of the Act is warranted.
We determined that issuing an
emergency regulation temporarily
listing the species is not warranted for
the Texas fawnsfoot at this time,
because we have not identified a threat
or activity that poses a significant risk,
such that losses to the species during
the normal listing process would
endanger the continued existence of the
entire species. However, if at any time
we determine that issuing an emergency
regulation temporarily listing the Texas
fawnsfoot is warranted, we will initiate
this action at that time.
Listing Priority Number for Texas
Fawnsfoot
The Service adopted guidelines on
September 21, 1983 (48 FR 43098), to
establish a rational system for utilizing
available resources for the highest
priority species when adding species to
the Lists of Endangered and Threatened
Wildlife and Plants or reclassifying
species listed as threatened to
endangered status. These guidelines,
titled ‘‘Endangered and Threatened
Species Listing and Recovery Priority
Guidelines’’ address the immediacy and
magnitude of threats, and the level of
taxonomic distinctiveness by assigning
priority in descending order to
monotypic genera (genus with one
species), full species, and subspecies (or
equivalently, distinct population
segments of vertebrates).
As a result of our analysis of the best
available scientific and commercial
information, we have assigned the Texas
fawnsfoot an LPN of 2, based on our
finding that the species faces threats
that are of high magnitude and are
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imminent. These threats include habitat
loss and degradation from
impoundments, sedimentation, sand
and gravel mining, and chemical
contaminants; other natural or
manmade factors such as climate
change, small, isolated populations, and
nonnative species; and the fact that the
threats to the species are not being
adequately addressed by existing
regulatory mechanisms. Our rationale
for assigning the Texas fawnsfoot an
LPN of 2 is outlined below.
We consider the threats that the Texas
fawnsfoot faces to be high in magnitude.
Habitat loss and degradation from
impoundments, sedimentation, sand
and gravel mining, and chemical
contaminants are widespread
throughout the range of the Texas
fawnsfoot and profoundly affect its
habitat. Remaining populations are
small, isolated, and highly vulnerable to
stochastic events.
Under our LPN guidelines, the second
criterion we consider in assigning a
listing priority is the immediacy of
threats. We consider the threats to the
Texas fawnsfoot as described under
Factors A, D, and E in the Five-Factor
Evaluation for Texas Fawnsfoot section
to be imminent because these threats are
ongoing and will continue in the
foreseeable future. Habitat loss and
destruction has already occurred and
will continue as the human population
continues to grow in central Texas. The
Texas fawnsfoot populations may
already be below the minimum viable
population requirement, which would
cause a reduction in the number of
populations and an increase in the
species’ vulnerability to extinction.
These threats are exacerbated by climate
change, which will increase the
frequency and magnitude of droughts.
Therefore, we consider these threats to
be imminent.
Thirdly, the Texas fawnsfoot is a valid
taxon at the species level and, therefore,
receives a higher priority than
subspecies, but a lower priority than
species in a monotypic genus.
Therefore, we assigned Texas fawnsfoot
an LPN of 2. We will continue to
monitor the threats to the Texas
fawnsfoot and the species’ status on an
annual basis, and should the magnitude
or imminence of the threats change, we
will revisit our assessment of the LPN.
While we conclude that listing the
Texas fawnsfoot is warranted, an
immediate proposal to list this species
is precluded by other higher priority
listings, which we address in the
Preclusion and Expeditious Progress
section below. Because we have
assigned the Texas fawnsfoot an LPN of
2, work on a proposed listing
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determination for the species is
precluded by work on higher priority
listing actions with absolute statutory,
court-ordered, or court-approved
deadlines and final listing
determinations for those species that
were proposed for listing with funds
from Fiscal Year (FY) 2011. This work
includes all the actions listed in the
tables below under Preclusion and
Expeditious Progress.
Preclusion and Expeditious Progress
Preclusion is a function of the listing
priority of a species in relation to the
resources that are available and the cost
and relative priority of competing
demands for those resources. Thus, in
any given fiscal year (FY), multiple
factors dictate whether it will be
possible to undertake work on a listing
proposal regulation or whether
promulgation of such a proposal is
precluded by higher priority listing
actions.
The resources available for listing
actions are determined through the
annual Congressional appropriations
process. The appropriation for the
Listing Program is available to support
work involving the following listing
actions: Proposed and final listing rules;
90-day and 12-month findings on
petitions to add species to the Lists of
Endangered and Threatened Wildlife
and Plants (Lists) or to change the status
of a species from threatened to
endangered; annual ‘‘resubmitted’’
petition findings on prior warrantedbut-precluded petition findings as
required under section 4(b)(3)(C)(i) of
the Act; critical habitat petition
findings; proposed and final rules
designating critical habitat; and
litigation-related, administrative, and
program-management functions
(including preparing and allocating
budgets, responding to Congressional
and public inquiries, and conducting
public outreach regarding listing and
critical habitat). The work involved in
preparing various listing documents can
be extensive and may include, but is not
limited to: Gathering and assessing the
best scientific and commercial data
available and conducting analyses used
as the basis for our decisions; writing
and publishing documents; and
obtaining, reviewing, and evaluating
public comments and peer review
comments on proposed rules and
incorporating relevant information into
final rules. The number of listing
actions that we can undertake in a given
year also is influenced by the
complexity of those listing actions; that
is, more complex actions generally are
more costly. The median cost for
preparing and publishing a 90-day
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finding is $39,276; for a 12-month
finding, $100,690; for a proposed rule
with critical habitat, $345,000; and for
a final listing rule with critical habitat,
$305,000.
We cannot spend more than is
appropriated for the Listing Program
without violating the Anti-Deficiency
Act (see 31 U.S.C. 1341(a)(1)(A)). In
addition, in FY 1998 and for each fiscal
year since then, Congress has placed a
statutory cap on funds that may be
expended for the Listing Program, equal
to the amount expressly appropriated
for that purpose in that fiscal year. This
cap was designed to prevent funds
appropriated for other functions under
the Act (for example, recovery funds for
removing species from the Lists), or for
other Service programs, from being used
for Listing Program actions (see House
Report 105–163, 105th Congress, 1st
Session, July 1, 1997).
Since FY 2002, the Service’s budget
has included a critical habitat subcap to
ensure that some funds are available for
other work in the Listing Program (‘‘The
critical habitat designation subcap will
ensure that some funding is available to
address other listing activities’’ (House
Report No. 107–103, 107th Congress, 1st
Session, June 19, 2001)). In FY 2002 and
each year until FY 2006, the Service has
had to use virtually the entire critical
habitat subcap to address courtmandated designations of critical
habitat, and consequently none of the
critical habitat subcap funds have been
available for other listing activities. In
some FYs since 2006, we have been able
to use some of the critical habitat
subcap funds to fund proposed listing
determinations for high-priority
candidate species. In other FYs, while
we were unable to use any of the critical
habitat subcap funds to fund proposed
listing determinations, we did use some
of this money to fund the critical habitat
portion of some proposed listing
determinations so that the proposed
listing determination and proposed
critical habitat designation could be
combined into one rule, thereby being
more efficient in our work. At this time,
for FY 2011, we plan to use some of the
critical habitat subcap funds to fund
proposed listing determinations.
We make our determinations of
preclusion on a nationwide basis to
ensure that the species most in need of
listing will be addressed first and also
because we allocate our listing budget
on a nationwide basis. Through the
listing cap, the critical habitat subcap,
and the amount of funds needed to
address court-mandated critical habitat
designations, Congress and the courts
have in effect determined the amount of
money available for other listing
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activities nationwide. Therefore, the
funds in the listing cap, other than those
needed to address court-mandated
critical habitat for already listed species,
set the limits on our determinations of
preclusion and expeditious progress.
Congress identified the availability of
resources as the only basis for deferring
the initiation of a rulemaking that is
warranted. The Conference Report
accompanying Public Law 97–304
(Endangered Species Act Amendments
of 1982), which established the current
statutory deadlines and the warrantedbut-precluded finding, states that the
amendments were ‘‘not intended to
allow the Secretary to delay
commencing the rulemaking process for
any reason other than that the existence
of pending or imminent proposals to list
species subject to a greater degree of
threat would make allocation of
resources to such a petition [that is, for
a lower-ranking species] unwise.’’
Although that statement appeared to
refer specifically to the ‘‘to the
maximum extent practicable’’ limitation
on the 90-day deadline for making a
‘‘substantial information’’ finding, that
finding is made at the point when the
Service is deciding whether or not to
commence a status review that will
determine the degree of threats facing
the species, and therefore the analysis
underlying the statement is more
relevant to the use of the warranted-butprecluded finding, which is made when
the Service has already determined the
degree of threats facing the species and
is deciding whether or not to commence
a rulemaking.
In FY 2011, on April 15, 2011,
Congress passed the Full-Year
Continuing Appropriations Act (Pub. L.
112–10), which provides funding
through September 30, 2011. The
Service has $20,902,000 for the listing
program. Of that, $9,472,000 is being
used for determinations of critical
habitat for already listed species. Also
$500,000 is appropriated for foreign
species listings under the Act. The
Service thus has $10,930,000 available
to fund work in the following categories:
Compliance with court orders and
court-approved settlement agreements
requiring that petition findings or listing
determinations be completed by a
specific date; section 4 (of the Act)
listing actions with absolute statutory
deadlines; essential litigation-related,
administrative, and listing programmanagement functions; and highpriority listing actions for some of our
candidate species. In FY 2010, the
Service received many new petitions
and a single petition to list 404 species.
The receipt of petitions for a large
number of species is consuming the
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Service’s listing funding that is not
dedicated to meeting court-ordered
commitments. Absent some ability to
balance effort among listing duties
under existing funding levels, the
Service is only able to initiate a few new
listing determinations for candidate
species in FY 2011.
In 2009, the responsibility for listing
foreign species under the Act was
transferred from the Division of
Scientific Authority, International
Affairs Program, to the Endangered
Species Program. Therefore, starting in
FY 2010, we used a portion of our
funding to work on the actions
described above for listing actions
related to foreign species. In FY 2011,
we anticipate using $1,500,000 for work
on listing actions for foreign species,
which reduces funding available for
domestic listing actions; however,
currently only $500,000 has been
allocated for this function. Although
there are no foreign species issues
included in our high-priority listing
actions at this time, many actions have
statutory or court-approved settlement
deadlines, thus increasing their priority.
The budget allocations for each specific
listing action are identified in the
Service’s FY 2011 Allocation Table (part
of our record).
For the above reasons, funding
proposed listing determinations for the
Texas fatmucket, golden orb, smooth
pimpleback, Texas pimpleback, and
Texas fawnsfoot is precluded by courtordered and court-approved settlement
agreements, listing actions with absolute
statutory deadlines, and work on
proposed listing determinations for
those candidate species with a higher
listing priority (i.e., candidate species
with LPNs of 1).
Based on our September 21, 1983,
guidelines for assigning an LPN for each
candidate species (48 FR 43098), we
have a significant number of species
with a LPN of 2. Using these guidelines,
we assign each candidate an LPN of 1
to 12, depending on the magnitude of
threats (high or moderate to low),
immediacy of threats (imminent or
nonimminent), and taxonomic status of
the species (in order of priority:
monotypic genus (a species that is the
sole member of a genus); species; or part
of a species (subspecies, or distinct
population segment)). The lower the
listing priority number, the higher the
listing priority (that is, a species with an
LPN of 1 would have the highest listing
priority).
Because of the large number of highpriority species, we have further ranked
the candidate species with an LPN of 2
by using the following extinction-risk
type criteria: International Union for the
Conservation of Nature and Natural
Resources (IUCN) Red list status/rank,
Heritage rank (provided by
NatureServe), Heritage threat rank
(provided by NatureServe), and species
currently with fewer than 50
individuals, or 4 or fewer populations.
Those species with the highest IUCN
rank (critically endangered), the highest
Heritage rank (G1), the highest Heritage
threat rank (substantial, imminent
threats), and currently with fewer than
50 individuals, or fewer than 4
populations, originally comprised a
group of approximately 40 candidate
species (‘‘Top 40’’). These 40 candidate
species have had the highest priority to
receive funding to work on a proposed
listing determination. As we work on
proposed and final listing rules for those
40 candidates, we apply the ranking
criteria to the next group of candidates
with an LPN of 2 and 3 to determine the
next set of highest priority candidate
species. Finally, proposed rules for
reclassification of threatened species to
endangered species are lower priority,
because as listed species, they are
already afforded the protections of the
Act and implementing regulations.
However, for efficiency reasons, we may
choose to work on a proposed rule to
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reclassify a species to endangered if we
can combine this with work that is
subject to a court-determined deadline.
With our workload so much bigger
than the amount of funds we have to
accomplish it, it is important that we be
as efficient as possible in our listing
process. Therefore, as we work on
proposed rules for the highest priority
species in the next several years, we are
preparing multi-species proposals when
appropriate, and these may include
species with lower priority if they
overlap geographically or have the same
threats as a species with an LPN of 2.
In addition, we take into consideration
the availability of staff resources when
we determine which high-priority
species will receive funding to
minimize the amount of time and
resources required to complete each
listing action.
As explained above, a determination
that listing is warranted but precluded
must also demonstrate that expeditious
progress is being made to add and
remove qualified species to and from
the Lists of Endangered and Threatened
Wildlife and Plants. As with our
‘‘precluded’’ finding, the evaluation of
whether progress in adding qualified
species to the Lists has been expeditious
is a function of the resources available
for listing and the competing demands
for those funds. (Although we do not
discuss it in detail here, we are also
making expeditious progress in
removing species from the list under the
Recovery program in light of the
resource available for delisting, which is
funded by a separate line item in the
budget of the Endangered Species
Program. So far during FY 2011, we
have completed delisting rules for three
species.) Given the limited resources
available for listing, we find that we are
making expeditious progress in FY 2011
in the Listing Program. This progress
included preparing and publishing the
following determinations:
FY 2011 COMPLETED LISTING ACTIONS
Publication date
Title
Actions
FR Pages
10/6/2010 ..........
Endangered Status for the Altamaha Spinymussel
and Designation of Critical Habitat.
12-Month Finding on a Petition to list the Sacramento
Splittail as Endangered or Threatened.
Endangered Status and Designation of Critical Habitat
for Spikedace and Loach Minnow.
90-Day Finding on a Petition to List the Bay Springs
Salamander as Endangered.
Determination of Endangered Status for the Georgia
Pigtoe Mussel, Interrupted Rocksnail, and Rough
Hornsnail and Designation of Critical Habitat.
Listing the Rayed Bean and Snuffbox as Endangered
Proposed Listing Endangered ........................
75 FR 61664–61690
Notice of 12-month petition finding, Not warranted.
Proposed Listing Endangered (uplisting) .......
75 FR 62070–62095
mstockstill on DSK4VPTVN1PROD with PROPOSALS2
10/7/2010 ..........
10/28/2010 ........
11/2/2010 ..........
11/2/2010 ..........
11/2/2010 ..........
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75 FR 66481–66552
Notice of 90-day Petition Finding, Not substantial.
Final Listing Endangered ...............................
75 FR 67511–67550
Proposed Listing Endangered ........................
75 FR 67551–67583
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75 FR 67341–67343
62208
Federal Register / Vol. 76, No. 194 / Thursday, October 6, 2011 / Proposed Rules
FY 2011 COMPLETED LISTING ACTIONS—Continued
Publication date
Title
Actions
FR Pages
11/4/2010 ..........
12-Month Finding on a Petition to List Cirsium wrightii
(Wright’s Marsh Thistle) as Endangered or Threatened.
Endangered Status for Dunes Sagebrush Lizard ........
12-Month Finding on a Petition to List the North
American Wolverine as Endangered or Threatened.
12-Month Finding on a Petition to List the Sonoran
Population of the Desert Tortoise as Endangered or
Threatened.
12-Month Finding on a Petition to List Astragalus
microcymbus and Astragalus schmolliae as Endangered or Threatened.
Listing Seven Brazilian Bird Species as Endangered
Throughout Their Range.
90-Day Finding on a Petition to List the Red Knot
subspecies Calidris canutus roselaari as Endangered.
Endangered Status for the Sheepnose and
Spectaclecase Mussels.
12-Month Finding on a Petition to List the Pacific Walrus as Endangered or Threatened.
90-Day Finding on a Petition to List the Sand Verbena Moth as Endangered or Threatened.
Determination of Threatened Status for the New Zealand-Australia Distinct Population Segment of the
Southern Rockhopper Penguin.
12-Month Finding on a Petition to List Solanum
conocarpum (marron bacora) as Endangered.
12-Month Finding on a Petition to List Thorne’s
Hairstreak Butterfly as Endangered.
12-Month Finding on a Petition to List Astragalus
hamiltonii,
Penstemon
flowersii,
Eriogonum
soredium, Lepidium ostleri, and Trifolium friscanum
as Endangered or Threatened.
90-Day Finding on a Petition to List the Wild Plains
Bison or Each of Four Distinct Population Segments as Threatened.
90-Day Finding on a Petition to List the Unsilvered
Fritillary Butterfly as Threatened or Endangered.
12-Month Finding on a Petition to List the Mt.
Charleston Blue Butterfly as Endangered or Threatened.
90-Day Finding on a Petition to List the Texas Kangaroo Rat as Endangered or Threatened.
Initiation of Status Review for Longfin Smelt ...............
Withdrawal of Proposed Rule to List the Flat-tailed
Horned Lizard as Threatened.
Proposed Threatened Status for the Chiricahua Leopard Frog and Proposed Designation of Critical Habitat.
12-Month Finding on a Petition to List the Berry Cave
Salamander as Endangered.
90-Day Finding on a Petition to List the Spring Pygmy
Sunfish as Endangered.
12-Month Finding on a Petition to List the Bearmouth
Mountainsnail, Byrne Resort Mountainsnail, and
Meltwater Lednian Stonefly as Endangered or
Threatened.
90-Day Finding on a Petition to List the Peary Caribou and Dolphin and Union population of the Barren-ground Caribou as Endangered or Threatened.
Proposed Endangered Status for the Three Forks
Springsnail and San Bernardino Springsnail, and
Proposed Designation of Critical Habitat.
90-Day Finding on a Petition to List Spring Mountains
Acastus Checkerspot Butterfly as Endangered.
90-Day Finding on a Petition to List the Prairie Chub
as Threatened or Endangered.
12-Month Finding on a Petition to List Hermes Copper
Butterfly as Endangered or Threatened.
90-Day Finding on a Petition to List the Arapahoe
Snowfly as Endangered or Threatened.
Notice of 12-month petition finding, Warranted but precluded.
75 FR 67925–67944
Proposed Listing Endangered ........................
Notice of 12-month petition finding, Warranted but precluded.
Notice of 12-month petition finding, Warranted but precluded.
75 FR 77801–77817
75 FR 78029–78061
Notice of 12-month petition finding, Warranted but precluded.
75 FR 78513–78556
Final Listing Endangered ...............................
75 FR 81793–81815
Notice of 90-day Petition Finding, Not substantial.
76 FR 304–311
Proposed Listing Endangered ........................
76 FR 3392–3420
Notice of 12-month petition finding, Warranted but precluded.
Notice of 90-day Petition Finding, Substantial
76 FR 7634–7679
76 FR 9309–9318
Final Listing Threatened ................................
76 FR 9681–9692
Notice of 12-month petition finding, Warranted but precluded.
Notice of 12-month petition finding, Not warranted.
Notice of 12-month petition finding, Warranted but precluded & Not Warranted.
76 FR 9722–9733
Notice of 90-day Petition Finding, Not substantial.
76 FR 10299–10310
Notice of 90-day Petition Finding, Not substantial.
Notice of 12-month petition finding, Warranted but precluded.
76 FR 10310–10319
Notice of 90-day Petition Finding, Substantial
76 FR 12683–12690
Notice of Status Review .................................
Proposed rule withdrawal ...............................
76 FR 13121–13122
76 FR 14210–14268
Proposed Listing Threatened; Proposed Designation of Critical Habitat.
76 FR 14126–14207
Notice of 12-month petition finding, Warranted but precluded.
Notice of 90-day Petition Finding, Substantial
76 FR 15919–15932
12/14/2010 ........
12/14/2010 ........
12/14/2010 ........
12/15/2010 ........
12/28/2010 ........
1/4/2011 ............
1/19/2011 ..........
2/10/2011 ..........
2/17/2011 ..........
2/22/2011 ..........
2/22/2011 ..........
2/23/2011 ..........
2/23/2011 ..........
2/24/2011 ..........
2/24/2011 ..........
3/8/2011 ............
3/8/2011 ............
3/10/2011 ..........
3/15/2011 ..........
3/15/2011 ..........
3/22/2011 ..........
4/1/2011 ............
4/5/2011 ............
mstockstill on DSK4VPTVN1PROD with PROPOSALS2
4/5/2011 ............
4/12/2011 ..........
4/13/2011 ..........
4/14/2011 ..........
4/14/2011 ..........
4/26/2011 ..........
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75 FR 78093–78146
76 FR 9991–10003
76 FR 10166–10203
76 FR 12667–12683
76 FR 18138–18143
Notice of 12-month petition finding, Not Warranted and Warranted but precluded.
76 FR 18684–18701
Notice of 90-day Petition Finding, Substantial
76 FR 18701–18706
Proposed Listing Endangered;
Designation of Critical Habitat.
Proposed
76 FR 20464–20488
Notice of 90-day Petition Finding, Substantial
76 FR 20613–20622
Notice of 90-day Petition Finding, Substantial
76 FR 20911–20918
Notice of 12-month petition finding, Warranted but precluded.
Notice of 90-day Petition Finding, Substantial
76 FR 20918–20939
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76 FR 23256–23265
Federal Register / Vol. 76, No. 194 / Thursday, October 6, 2011 / Proposed Rules
62209
FY 2011 COMPLETED LISTING ACTIONS—Continued
Publication date
Title
Actions
FR Pages
4/26/2011 ..........
90-Day Finding on a Petition to List the Smooth-Billed
Ani as Threatened or Endangered.
Withdrawal of the Proposed Rule to List the Mountain
Plover as Threatened.
90-Day Finding on a Petition to List the Spot-tailed
Earless Lizard as Endangered or Threatened.
Listing the Salmon-Crested Cockatoo as Threatened
Throughout its Range with Special Rule.
12-Month Finding on a Petition to List Puerto Rican
Harlequin Butterfly as Endangered.
90-Day Finding on a Petition to Reclassify the
Straight-Horned Markhor (Capra falconeri jerdoni)
of Torghar Hills as Threatened.
90-Day Finding on a Petition to List the Goldenwinged Warbler as Endangered or Threatened.
12-Month Finding on a Petition to List the Striped
Newt as Threatened.
12-Month Finding on a Petition to List Abronia
ammophila,
Agrostis
rossiae,
Astragalus
proimanthus, Boechera (Arabis) pusilla, and
Penstemon gibbensii as Threatened or Endangered.
90-Day Finding on a Petition to List the Utah Population of the Gila Monster as an Endangered or a
Threatened Distinct Population Segment.
Revised 90-Day Finding on a Petition to Reclassify
the Utah Prairie Dog From Threatened to Endangered.
12-Month Finding on a Petition to List Castanea
pumila var. ozarkensis as Threatened or Endangered.
90-Day Finding on a Petition to List the Eastern
Small-Footed Bat and the Northern Long-Eared Bat
as Threatened or Endangered.
12-Month Finding on a Petition to List a Distinct Population Segment of the Fisher in Its United States
Northern Rocky Mountain Range as Endangered or
Threatened with Critical Habitat.
90-Day Finding on a Petition to List the Bay Skipper
as Threatened or Endangered.
12-Month Finding on a Petition to List Pinus albicaulis
as Endangered or Threatened with Critical Habitat.
Petition to List Grand Canyon Cave Pseudoscorpion ..
Notice of 90-day Petition Finding, Not substantial.
Proposed Rule, Withdrawal ...........................
76 FR 23265–23271
76 FR 27756–27799
Notice of 90-day Petition Finding, Substantial
76 FR 30082–30087
Final Listing Threatened ................................
76 FR 30758–30780
Notice of 12-month petition finding, Warranted but precluded.
Notice of 90-day Petition Finding, Substantial
76 FR 31282–31294
76 FR 31903–31906
Notice of 90-day Petition Finding, Substantial
76 FR 31920–31926
Notice of 12-month petition finding, Warranted but precluded.
Notice of 12-month petition finding, Not Warranted and Warranted but precluded.
76 FR 32911–32929
76 FR 33924–33965
Notice of 90-day Petition Finding, Not substantial.
76 FR 36049–36053
Notice of 90-day Petition Finding, Not substantial.
76 FR 36053–36068
Notice of 12-month petition finding, Not warranted.
76 FR 37706–37716
Notice of 90-day Petition Finding, Substantial
76 FR 38095–38106
Notice of 12-month petition finding, Not warranted.
76 FR 38504–38532
Notice of 90-day Petition Finding, Substantial
76 FR 40868–40871
Notice of 12-month petition finding, Warranted but precluded.
Notice of 12-month petition finding, Not warranted.
Notice of 12-month petition finding, Not warranted.
76 FR 42631–42654
Notice of 12-month petition finding, Not warranted.
Final Listing Endangered, Threatened ...........
76 FR 44566–44569
5/12/2011 ..........
5/25/2011 ..........
5/26/2011 ..........
5/31/2011 ..........
6/2/2011 ............
6/2/2011 ............
6/7/2011 ............
6/9/2011 ............
6/21/2011 ..........
6/21/2011 ..........
6/28/2011 ..........
6/29/2011 ..........
6/30/2011 ..........
7/12/2011 ..........
7/19/2011 ..........
7/19/2011 ..........
7/26/2011 ..........
7/26/2011 ..........
7/27/2011 ..........
7/27/2011 ..........
8/2/2011 ............
8/2/2011 ............
mstockstill on DSK4VPTVN1PROD with PROPOSALS2
8/2/2011 ............
8/2/2011 ............
8/4/2011 ............
8/9/2011 ............
8/9/2011 ............
VerDate Mar<15>2010
12-Month Finding on a Petition to List the Giant
Palouse Earthworm (Drilolerius americanus) as
Threatened or Endangered.
12-Month Finding on a Petition to List the Frigid
Ambersnail as Endangered.
Determination of Endangered Status for Ipomopsis
polyantha (Pagosa Skyrocket) and Threatened Status for Penstemon debilis (Parachute Beardtongue)
and Phacelia submutica (DeBeque Phacelia).
12-Month Finding on a Petition to List the Gopher
Tortoise as Threatened in the Eastern Portion of its
Range.
Proposed Endangered Status for the Chupadera
Springsnail (Pyrgulopsis chupaderae) and Proposed
Designation of Critical Habitat.
90-Day Finding on a Petition to List the Straight
Snowfly and Idaho Snowfly as Endangered.
12-Month Finding on a Petition to List the Redrock
Stonefly as Endangered or Threatened.
Listing 23 Species on Oahu as Endangered and Designating Critical Habitat for 124 Species.
90-Day Finding on a Petition to List Six Sand Dune
Beetles as Endangered or Threatened.
Endangered Status for the Cumberland Darter, Rush
Darter, Yellowcheek Darter, Chucky Madtom, and
Laurel Dace.
12-Month Finding on a Petition to List the Nueces
River and Plateau Shiners as Threatened or Endangered.
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76 FR 42654–42658
76 FR 44547–44564
76 FR 45054–45075
Notice of 12-month petition finding, Warranted but precluded.
76 FR 45130–45162
Proposed Listing Endangered ........................
76 FR 46218–46234
Notice of 90-day Petition Finding, Not substantial.
Notice of 12-month petition finding, Not warranted.
Proposed Listing Endangered ........................
76 FR 46238–46251
Notice of 90-day Petition Finding, Not substantial and substantial.
Final Listing Endangered ...............................
Notice of 12-month petition finding, Not warranted.
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76 FR 46251–46266
76 FR 46362–46594
76 FR 47123–47133
76 FR 48722–48741
76 FR 48777–48788
62210
Federal Register / Vol. 76, No. 194 / Thursday, October 6, 2011 / Proposed Rules
FY 2011 COMPLETED LISTING ACTIONS—Continued
Publication date
Title
Actions
FR Pages
8/9/2011 ............
Four Foreign Parrot Species [crimson shining parrot,
white cockatoo, Philippine cockatoo, yellow-crested
cockatoo].
Proposed Listing of the Miami Blue Butterfly as Endangered, and Proposed Listing of the Cassius
Blue, Ceraunus Blue, and Nickerbean Blue Butterflies as Threatened Due to Similarity of Appearance
to the Miami Blue Butterfly.
90-Day Finding on a Petition to List the Saltmarsh
Topminnow as Threatened or Endangered Under
the Endangered Species Act.
Proposed Listing of the Miami Blue Butterfly as Endangered, and Proposed Listing of the Cassius
Blue, Ceraunus Blue, and Nickerbean Blue Butterflies as Threatened Due to Similarity of Appearance
to the Miami Blue Butterfly.
Emergency Listing of the Miami Blue Butterfly as Endangered, and Emergency Listing of the Cassius
Blue, Ceraunus Blue, and Nickerbean Blue Butterflies as Threatened Due to Similarity of Appearance
to the Miami Blue Butterfly.
Listing Six Foreign Birds as Endangered Throughout
Their Range.
90-Day Finding on a Petition to List the Leona’s Little
Blue Butterfly as Endangered or Threatened.
90-Day Finding on a Petition to List All Chimpanzees
(Pan troglodytes) as Endangered.
12-Month Finding on Five Petitions to List Seven Species of Hawaiian Yellow-faced Bees as Endangered.
12-Month Petition Finding and Proposed Listing of
Arctostaphylos franciscana as Endangered.
90-Day Finding on a Petition to List the Snowy Plover
and Reclassify the Wintering Population of Piping
Plover.
90-Day Finding on a Petition to List the Franklin’s
Bumble Bee as Endangered.
90-Day Finding on a Petition to List 42 Great Basin
and Mojave Desert Springsnails as Threatened or
Endangered with Critical Habitat.
Proposed Listing Endangered and Threatened; Notice of 12-month petition finding,
Not warranted.
Proposed Listing Endangered Similarity of
Appearance.
76 FR 49202–49236
Notice of 90-day Petition Finding, Substantial
76 FR 49412–49417
Proposed Listing Endangered and Similarity
of Appearance.
76 FR 49408–49412
Emergency Listing Endangered and Similarity of Appearance.
76 FR 49542–49567
Final Listing Endangered ...............................
76 FR 50052–50080
Notice of 90-day Petition Finding, Substantial
76 FR 50971–50979
Notice of 90-day Petition Finding, Substantial
76 FR 54423–54425
Notice of 12-month petition finding, Warranted but precluded.
Notice of 12-month petition finding, Warranted; Proposed Listing Endangered.
Notice of 90-day Petition Finding, Not substantial.
76 FR 55170–55203
Notice of 90-day Petition Finding, Substantial
76 FR
Notice of 90-day Petition Finding, Substantial
and Not substantial.
76 FR
8/10/2011 ..........
8/10/2011 ..........
8/10/2011 ..........
8/10/2011 ..........
8/11/2011 ..........
8/17/2011 ..........
9/01/2011 ..........
9/6/2011 ............
9/8/2011 ............
9/8/2011 ............
9/13/2011 ..........
9/13/2011 ..........
Our expeditious progress also
includes work on listing actions that we
funded in FY 2010 and FY 2011 but
have not yet been completed to date.
These actions are listed below. Actions
in the top section of the table are being
conducted under a deadline set by a
court. Actions in the middle section of
the table are being conducted to meet
statutory timelines, that is, timelines
required under the Act. Actions in the
bottom section of the table are highpriority listing actions. These actions
include work primarily on species with
an LPN of 2, and, as discussed above,
selection of these species is partially
based on available staff resources, and
when appropriate, include species with
76 FR 49408–49412
76 FR 55623–55638
76 FR 55638–55641
a lower priority if they overlap
geographically or have the same threats
as the species with the high priority.
Including these species together in the
same proposed rule results in
considerable savings in time and
funding, when compared to preparing
separate proposed rules for each of them
in the future.
ACTIONS FUNDED IN FY 2010 AND FY 2011 BUT NOT YET COMPLETED
Species
Action
mstockstill on DSK4VPTVN1PROD with PROPOSALS2
Actions Subject to Court Order/Settlement Agreement
4 parrot species (military macaw, yellow-billed parrot, red-crowned parrot, scarlet macaw) 5 ........
4 parrot species (blue-headed macaw, great green macaw, grey-cheeked parakeet, hyacinth
macaw) 5.
Longfin smelt .....................................................................................................................................
12-month petition finding.
12-month petition finding.
12-month petition finding.
Actions with Statutory Deadlines
Casey’s june beetle ...........................................................................................................................
5 Bird species from Colombia and Ecuador .....................................................................................
Queen Charlotte goshawk ................................................................................................................
Ozark hellbender 4 .............................................................................................................................
Altamaha spinymussel 3 ....................................................................................................................
6 Birds from Peru & Bolivia ..............................................................................................................
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Final
Final
Final
Final
Final
Final
E:\FR\FM\06OCP2.SGM
listing
listing
listing
listing
listing
listing
determination.
determination.
determination.
determination.
determination.
determination.
06OCP2
Federal Register / Vol. 76, No. 194 / Thursday, October 6, 2011 / Proposed Rules
62211
ACTIONS FUNDED IN FY 2010 AND FY 2011 BUT NOT YET COMPLETED—Continued
Species
Action
Loggerhead sea turtle (assist National Marine Fisheries Service) 5 .................................................
2 mussels (rayed bean (LPN = 2), snuffbox No LPN) 5 ...................................................................
CA golden trout 4 ...............................................................................................................................
Black-footed albatross .......................................................................................................................
Mojave fringe-toed lizard 1 .................................................................................................................
Kokanee—Lake Sammamish population 1 ........................................................................................
Cactus ferruginous pygmy-owl 1 ........................................................................................................
Northern leopard frog ........................................................................................................................
Tehachapi slender salamander .........................................................................................................
Coqui Llanero ....................................................................................................................................
Dusky tree vole. ................................................................................................................................
Leatherside chub (from 206 species petition) ..................................................................................
Platte River caddisfly (from 206 species petition) 5 ..........................................................................
3 Texas moths (Ursia furtiva, Sphingicampa blanchardi, Agapema galbina) (from 475 species
petition).
3 South Arizona plants (Erigeron piscaticus, Astragalus hypoxylus, Amoreuxia gonzalezii) (from
475 species petition).
14 parrots (foreign species) ..............................................................................................................
Mohave Ground Squirrel 1 .................................................................................................................
Western gull-billed tern .....................................................................................................................
OK grass pink (Calopogon oklahomensis) 1 .....................................................................................
Ashy storm-petrel 5 ............................................................................................................................
Honduran emerald ............................................................................................................................
Eagle Lake trout 1 ..............................................................................................................................
32 Pacific Northwest mollusks species (snails and slugs) 1 .............................................................
Spring Mountains checkerspot butterfly ............................................................................................
10 species of Great Basin butterfly ..................................................................................................
404 Southeast species ......................................................................................................................
American eel 4 ...................................................................................................................................
Aztec gilia 5 ........................................................................................................................................
White-tailed ptarmigan 5 ....................................................................................................................
San Bernardino flying squirrel 5 .........................................................................................................
Bicknell’s thrush 5 ..............................................................................................................................
Sonoran talussnail 5 ...........................................................................................................................
2 AZ Sky Island plants (Graptopetalum bartrami & Pectis imberbis) 5 .............................................
I’iwi 5 ..................................................................................................................................................
Humboldt marten ...............................................................................................................................
Desert massasauga ..........................................................................................................................
Western glacier stonefly (Zapada glacier) ........................................................................................
Thermophilic ostracod (Potamocypris hunteri) .................................................................................
Sierra Nevada red fox 5 .....................................................................................................................
Boreal toad (eastern or southern Rocky Mtn population) 5 ..............................................................
Alexander Archipelago wolf 5 ............................................................................................................
Final listing determination.
Final listing determination.
12-month petition finding.
12-month petition finding.
12-month petition finding.
12-month petition finding.
12-month petition finding.
12-month petition finding.
12-month petition finding.
12-month petition finding/Proposed listing.
12-month petition finding.
12-month petition finding.
12-month petition finding.
12-month petition finding.
12-month petition finding.
12-month petition finding.
12-month petition finding.
12-month petition finding.
12-month petition finding.
12-month petition finding.
12-month petition finding.
90-day petition finding.
90-day petition finding.
90-day petition finding.
90-day petition finding.
90-day petition finding.
90-day petition finding.
90-day petition finding.
90-day petition finding.
90-day petition finding.
90-day petition finding.
90-day petition finding.
90-day petition finding.
90-day petition finding.
90-day petition finding.
90-day petition finding.
90-day petition finding.
90-day petition finding.
90-day petition finding.
90-day petition finding.
90-day petition finding.
mstockstill on DSK4VPTVN1PROD with PROPOSALS2
High-Priority Listing Actions
20 Maui-Nui candidate species 2 (17 plants, 3 tree snails) (14 with LPN = 2, 2 with LPN = 3, 3
with LPN = 8).
8 Gulf Coast mussels (southern kidneyshell (LPN = 2), round ebonyshell (LPN = 2), Alabama
pearlshell (LPN = 2), southern sandshell (LPN = 5), fuzzy pigtoe (LPN = 5), Choctaw bean
(LPN = 5), narrow pigtoe (LPN = 5), and tapered pigtoe (LPN = 11)) 4.
Umtanum buckwheat (LPN = 2) and white bluffs bladderpod (LPN = 9) 4 ......................................
Grotto sculpin (LPN = 2) 4 .................................................................................................................
2 Arkansas mussels (Neosho mucket (LPN = 2) & Rabbitsfoot (LPN = 9)) 4 ..................................
Diamond darter (LPN = 2) 4 ..............................................................................................................
Gunnison sage-grouse (LPN = 2) 4 ...................................................................................................
Coral Pink Sand Dunes Tiger Beetle (LPN = 2) 5 ............................................................................
Lesser prairie chicken (LPN = 2) ......................................................................................................
4 Texas salamanders (Austin blind salamander (LPN = 2), Salado salamander (LPN = 2),
Georgetown salamander (LPN = 8), Jollyville Plateau (LPN = 8)) 3.
5 SW aquatics (Gonzales Spring Snail (LPN = 2), Diamond Y springsnail (LPN = 2), Phantom
springsnail (LPN = 2), Phantom Cave snail (LPN = 2), Diminutive amphipod (LPN = 2)) 3.
2 Texas plants (Texas golden gladecress (Leavenworthia texana) (LPN = 2), Neches River rosemallow (Hibiscus dasycalyx) (LPN = 2)) 3.
4 AZ plants (Acuna cactus (Echinomastus erectocentrus var. acunensis) (LPN = 3), Fickeisen
plains cactus (Pediocactus peeblesianus fickeiseniae) (LPN = 3), Lemmon fleabane (Erigeron
lemmonii) (LPN = 8), Gierisch mallow (Sphaeralcea gierischii) (LPN = 2)) 5.
FL bonneted bat (LPN = 2) 3 .............................................................................................................
3 Southern FL plants (Florida semaphore cactus (Consolea corallicola) (LPN = 2), shellmound
applecactus (Harrisia (=Cereus) aboriginum (=gracilis)) (LPN = 2), Cape Sable thoroughwort
(Chromolaena frustrata) (LPN = 2)) 5.
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Proposed listing.
Proposed listing.
Proposed
Proposed
Proposed
Proposed
Proposed
Proposed
Proposed
Proposed
listing.
listing.
listing.
listing.
listing.
listing.
listing.
listing.
Proposed listing.
Proposed listing.
Proposed listing.
Proposed listing.
Proposed listing.
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62212
Federal Register / Vol. 76, No. 194 / Thursday, October 6, 2011 / Proposed Rules
ACTIONS FUNDED IN FY 2010 AND FY 2011 BUT NOT YET COMPLETED—Continued
Species
Action
21 Big Island (HI) species 5 (includes 8 candidate species—6 plants & 2 animals; 4 with LPN =
2, 1 with LPN = 3, 1 with LPN = 4, 2 with LPN = 8).
12 Puget Sound prairie species (9 subspecies of pocket gopher (Thomomys mazama ssp.)
(LPN = 3), streaked horned lark (LPN = 3), Taylor’s checkerspot (LPN = 3), Mardon skipper
(LPN = 8)) 3.
2 TN River mussels (fluted kidneyshell (LPN = 2), slabside pearlymussel (LPN = 2)) 5 .................
Jemez Mountain salamander (LPN = 2) 5 .........................................................................................
Proposed listing.
Proposed listing.
Proposed listing.
Proposed listing.
1 Funds
for listing actions for these species were provided in previous FYs.
funds for these high-priority listing actions were provided in FY 2008 or 2009, due to the complexity of these actions and competing
priorities, these actions are still being developed.
3 Partially funded with FY 2010 funds and FY 2011 funds.
4 Funded with FY 2010 funds.
5 Funded with FY 2011 funds.
2 Although
mstockstill on DSK4VPTVN1PROD with PROPOSALS2
We have endeavored to make our
listing actions as efficient and timely as
possible, given the requirements of the
relevant law and regulations, and
constraints relating to workload and
personnel. We are continually
considering ways to streamline
processes or achieve economies of scale,
such as by batching related actions
together. Given our limited budget for
implementing section 4 of the Act, these
actions described above collectively
constitute expeditious progress.
Texas fatmucket, golden orb, smooth
pimpleback, Texas pimpleback, and
Texas fawnsfoot will be added to the list
of candidate species upon publication of
this 12-month finding. We will continue
to evaluate these species as new
information becomes available.
VerDate Mar<15>2010
16:27 Oct 05, 2011
Jkt 226001
Continuing review will determine if a
change in status is warranted, including
the need to make prompt use of
emergency listing procedures.
We intend that any proposed listing
determination for Texas fatmucket,
golden orb, smooth pimpleback, Texas
pimpleback, and Texas fawnsfoot will
be as accurate as possible. Therefore, we
will continue to accept additional
information and comments from all
concerned governmental agencies, the
scientific community, industry, or any
other interested party concerning this
finding.
References Cited
A complete list of references cited is
available on the Internet at https://
www.regulations.gov and upon request
PO 00000
Frm 00048
Fmt 4701
Sfmt 9990
from the Clear Lake Ecological Services
Field Office (see ADDRESSES).
Authors
The primary authors of this notice are
the staff members from the Southwest
Region of the U.S. Fish and Wildlife
Service.
Authority
The authority for this section is
section 4 of the Endangered Species Act
of 1973, as amended (16 U.S.C. 1531 et
seq.).
Dated: September 26, 2011.
Rowan W. Gould,
Acting Director, Fish and Wildlife Service.
[FR Doc. 2011–25471 Filed 10–5–11; 8:45 am]
BILLING CODE 4310–55–P
E:\FR\FM\06OCP2.SGM
06OCP2
Agencies
[Federal Register Volume 76, Number 194 (Thursday, October 6, 2011)]
[Proposed Rules]
[Pages 62166-62212]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2011-25471]
[[Page 62165]]
Vol. 76
Thursday,
No. 194
October 6, 2011
Part II
Department of the Interior
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Fish and Wildlife Service
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50 CFR Part 17
Endangered and Threatened Wildlife and Plants; 12-Month Finding on a
Petition To List Texas Fatmucket, Golden Orb, Smooth Pimpleback, Texas
Pimpleback, and Texas Fawnsfoot as Threatened or Endangered; Proposed
Rule
Federal Register / Vol. 76 , No. 194 / Thursday, October 6, 2011 /
Proposed Rules
[[Page 62166]]
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DEPARTMENT OF THE INTERIOR
Fish and Wildlife Service
50 CFR Part 17
[FWS-R2-ES-2011-0079; MO 92210-0-0008 B2]
Endangered and Threatened Wildlife and Plants; 12-Month Finding
on a Petition To List Texas Fatmucket, Golden Orb, Smooth Pimpleback,
Texas Pimpleback, and Texas Fawnsfoot as Threatened or Endangered
AGENCY: Fish and Wildlife Service, Interior.
ACTION: Notice of 12-month petition finding.
-----------------------------------------------------------------------
SUMMARY: We, the U.S. Fish and Wildlife Service (Service), announce a
12-month finding on a petition to list five mussel species in Texas as
threatened or endangered and to designate critical habitat under the
Endangered Species Act of 1973, as amended (Act). The five species are
Texas fatmucket (Lampsilis bracteata), golden orb (Quadrula aurea),
smooth pimpleback (Q. houstonensis), Texas pimpleback (Q. petrina), and
Texas fawnsfoot (Truncilla macrodon). After review of all available
scientific and commercial information, we find that listing these five
mussel species is warranted. Currently, however, listing of these
species is precluded by higher priority actions to amend the Federal
Lists of Endangered and Threatened Wildlife and Plants. Upon
publication of this 12-month petition finding, we will add these five
species to our candidate species list. We will develop a proposed rule
to list these species as our priorities allow. We will make any
determination on critical habitat during development of the proposed
listing rule. In any interim period, we will address the status of the
candidate taxa through our annual Candidate Notice of Review.
DATES: The finding announced in this document was made on October 6,
2011.
ADDRESSES: This finding is available on the Internet at https://www.regulations.gov at Docket Number FWS-R2-ES-2011-0079. Supporting
documentation we used in preparing this finding is available for public
inspection, by appointment, during normal business hours at the U.S.
Fish and Wildlife Service, 1505 Ferguson Lane, Austin, TX 78754. Please
submit any new information, materials, comments, or questions
concerning this finding to the above address.
FOR FURTHER INFORMATION CONTACT: Gary Mowad, Texas State Administrator,
U.S. Fish and Wildlife Service (see ADDRESSES); by telephone at 512-
927-3557; or by facsimile at 512-927-3592. If you use a
telecommunications device for the deaf (TDD), please call the Federal
Information Relay Service (FIRS) at 800-877-8339.
SUPPLEMENTARY INFORMATION:
Background
Section 4(b)(3)(B) of the Act (16 U.S.C. 1531 et seq.) requires
that, for any petition to revise the Federal Lists of Endangered and
Threatened Wildlife and Plants that contains substantial scientific or
commercial information that listing the species may be warranted, we
make a finding within 12 months of the date of receipt of the petition.
In this finding, we will determine that the petitioned action is: (1)
Not warranted, (2) warranted, or (3) warranted, but the immediate
proposal of a regulation implementing the petitioned action is
precluded by other pending proposals to determine whether species are
threatened or endangered, and expeditious progress is being made to add
or remove qualified species from the Federal Lists of Endangered and
Threatened Wildlife and Plants. Section 4(b)(3)(C) of the Act requires
that we treat a petition for which the requested action is found to be
warranted but precluded as though resubmitted on the date of such
finding, that is, requiring a subsequent finding to be made within 12
months. We must publish these 12-month findings in the Federal
Register.
Previous Federal Actions
This 12-month petition finding covers five species of mussels that
are grouped together because of their overlapping or proximate ranges
within the river basins of central Texas. The petitions for listing
these five species were parts of two multi-species petitions, dated
June 18, 2007, and October 9, 2008. The other species from those
petitions, including other Texas mussels, will be considered in
separate petition findings.
On June 25, 2007, we received a formal petition dated June 18,
2007, from Forest Guardians (now WildEarth Guardians), requesting that
we: (1) Consider all full species in our Southwest Region ranked as G1
or G1G2 by the organization NatureServe, except those that are
currently listed, proposed for listing, or candidates for listing; and
(2) List each species as either threatened or endangered with critical
habitat. The petitioned group of species included four Texas mussels,
two of which are included in this finding: the Texas fatmucket and
golden orb. Two additional mussels from eastern Texas, the Texas
heelsplitter (Potamilus amphichaenus) and Salina mucket (P.
metnecktayi), were also included in this petition. The petition
incorporated all analyses, references, and documentation provided by
NatureServe in its online database at https://www.natureserve.org/ into
the petition. Included in NatureServe was supporting information
regarding the species' taxonomy and ecology, historical and current
distribution, present status, and actual and potential causes of
decline. We sent a letter dated July 11, 2007, to Forest Guardians
acknowledging receipt of the petition and stating that the petition was
under review by staff in our Southwest Regional Office.
On October 15, 2008, we received a petition dated October 9, 2008,
from WildEarth Guardians, requesting that the Service list as
threatened or endangered and designate critical habitat for six species
of freshwater mussels, including the smooth pimpleback, Texas
pimpleback, and Texas fawnsfoot. Two additional mussels from the Rio
Grande basin, the false spike (Quincuncina mitchelli) and Mexican
fawnsfoot (Truncilla congata), were also included in this petition. In
addition to other information, the petition incorporated all analyses,
references, and documentation provided by NatureServe in its online
database at https://www.natureserve.org/. In a November 26, 2008, letter
to the petitioner, we acknowledged receipt of the second petition and
stated that the petition for the six mussel species was under review by
staff in our Southwest (Region 2) and Southeast (Region 4) Regional
Offices. The southern hickorynut (Obovaria jacksoniana) was also
included in this 2008 petition, and on March 23, 2010 (75 FR 13717), we
found that the petition did not present substantial information
supporting that that species may be endanagered or threatened.
On December 15, 2009, we published our 90-day finding that the
petitions presented substantial scientific information indicating that
listing nine Texas mussels may be warranted (74 FR 66260). As a result
of the finding, we initiated a status review for all nine species. This
notice constitutes the 12-month finding on the June 18, 2007, petition
to list the Texas fatmucket and golden orb and the October 9, 2008,
petition to list the smooth pimpleback, Texas pimpleback, and Texas
fawnsfoot as threatened or endangered. Our petition findings for the
remaining Texas mussel species will be published at a later time.
[[Page 62167]]
Summary of Procedures for Determining the Listing Status of Species
Review of Status Based on Five Factors
Section 4 of the Act (16 U.S.C. 1533) and implementing regulations
(50 CFR part 424) set forth procedures for adding species to, removing
species from, or reclassifying species on the Federal Lists of
Endangered and Threatened Wildlife and Plants. Under section 4(a)(1) of
the Act, a species may be determined to be endangered or threatened
based on any of the following five factors:
(A) The present or threatened destruction, modification, or
curtailment of its habitat or range;
(B) Overutilization for commercial, recreational, scientific, or
educational purposes;
(C) Disease or predation;
(D) The inadequacy of existing regulatory mechanisms; or
(E) Other natural or manmade factors affecting its continued
existence.
In making these findings, we discuss below information pertaining
to each species in relation to the five factors provided in section
4(a)(1) of the Act. In considering what factors might constitute
threats to a species, we must look beyond the exposure of the species
to a particular factor to evaluate whether the species may respond to
the factor in a way that causes actual impacts to the species. If there
is exposure to a factor and the species responds negatively, the factor
may be a threat, and during the status review, we attempt to determine
how significant a threat it is. The threat is significant if it drives
or contributes to the risk of extinction of the species such that the
species warrants listing as endangered or threatened as those terms are
defined by the Act. However, the identification of factors that could
impact a species negatively may not be sufficient to compel a finding
that the species warrants listing. The information must include
evidence sufficient to suggest that the potential threat has the
capacity (i.e., it should be of sufficient magnitude and extent) to
affect the species' status such that it meets the definition of
endangered or threatened under the Act.
Evaluation of the Status of Each of the Five Mussel Species
In this finding, we first provide a description of general mussel
biology. Then, for each of the five species, we describe the species,
its life history, and habitat; evaluate listing factors for that
species; and present our finding that the petitioned action is
warranted or not for that species. We follow these descriptions,
evaluations, and findings with a discussion of the priority and
progress of our listing actions.
General Mussel Biology
All five species are freshwater mussels in the family Unionidae and
occur only in Texas, in portions of the Colorado, Guadalupe, Nueces-
Frio, and Brazos River systems (Howells et al. 1996, p. 1). Adult
freshwater mussels are suspension feeders, drawing in food and oxygen
through their incurrent siphon (tube that draws water into the shell).
They may also feed on organic particles in sediment using the large,
muscular foot (an organ used to anchor the mussel in the substrate or
for locomotion) (Raikow and Hamilton 2001, p. 520). Adults feed on
algae, bacteria, detritus (dead organic material), microscopic animals,
and dissolved organic matter (Fuller 1974, pp. 221-222; Silverman et
al. 1997, p. 1862; Nichols and Garling 2000, pp. 874-876; Christian et
al. 2004, p. 109). For their first several months, as they inhabit
interstitial spaces (small spaces between sediment particles) within
the substrate, juvenile mussels feed using cilia (fine hairs) on the
foot to capture suspended as well as depositional material, such as
algae and detritus (Yeager et al. 1994, pp. 253-259). Mussels tend to
grow relatively rapidly for the first few years, and then slow
appreciably at sexual maturity, when energy presumably is being
diverted from growth to reproductive activities (Baird 2000, pp. 66-
67).
As a group, mussels are extremely long lived, living from two to
several decades (Rogers et al. 2001, p. 592), and possibly up to 200
years in extreme instances (Bauer 1992, p. 427). Most mussel species,
including the five in this finding, have distinct forms of males and
females. During reproduction, males release clouds of sperm into the
water column, which females draw in through their siphons.
Fertilization takes place internally, and the resulting eggs develop
into specialized larvae (called glochidia) within the female gills. The
females release matured glochidia individually, in small groups, or
embedded in larger mucus structures called conglutinates.
The glochidia of freshwater mussels are obligate parasites (cannot
live independently of their hosts) on the gills or fins of fishes
(Vaughn and Taylor 1999, p. 913). Glochidia die if they fail to find a
host fish, attach to a fish that has developed immunity from prior
infestations, or attach to the wrong location on a host fish (Neves
1991, p. 254; Bogan 1993, p. 299). Glochidia encyst (enclose in a cyst-
like structure) on the host's tissue and develop into juvenile mussels
weeks or months after attachment (Arey 1932, pp. 214-215). Mussels
experience their primary opportunity for dispersal and movement within
the stream as glochidia attached to a host fish (Smith 1985, p. 105).
Upon release from the host, newly transformed juveniles drop to the
substrate on the bottom of the stream. Those juveniles that drop in
unsuitable substrates die because their immobility prevents them from
relocating to more favorable habitat. Juvenile freshwater mussels
burrow into interstitial substrates and grow to a larger size that is
less susceptible to predation and displacement from high flow events
(Yeager et al. 1994, p. 220). Throughout the rest of their life cycle,
mussels generally remain within the same small area where they released
from the host fish.
Species Information for Texas Fatmucket
Species Description
The Texas fatmucket is a large, elongated mussel that reaches a
maximum length of 100 millimeters (mm) (3.94 inches (in)) (Howells
2010c, p. 2). The shell is oval to elliptical or somewhat rhomboidal
and tan to greenish-yellow with numerous irregular, wavy, and broad and
narrow dark brown rays, with broad rays widening noticeably as they
approach the ventral (underside) margin. The nacre (inside of the
shell) is white with occasional yellow or salmon coloration and
iridescent posteriorly (Howells 2010c, p. 2). Females have mantle flaps
(extensions of the tissue that covers the visceral mass) that often
resemble minnows, including eye spots, lateral line, and fins (Howells
2010c, p. 2).
Taxonomy
The Texas fatmucket was first described in 1855 by Gould as Unio
bracteatus and later moved to the genus Lampsilis by Simpson (1900, p.
543). Some forms found in headwater streams were historically split
into a different species, L. elongatus, but they have since been
determined to be ecophenotypes (individuals whose shape is determined
by their environment) of L. bracteata (Howells 2010c, p. 5). The Texas
fatmucket is recognized by the Committee on Scientific and Vernacular
Names of Mollusks of the Council of Systematic Malacologists, American
Malacological Union (Turgeon et al. 1998, p. 34), and we recognize it
as a valid species.
[[Page 62168]]
Biology and Life History
Although there is no specific information on age and size of
maturity of the Texas fatmucket, it is likely similar to a related
species, the Louisiana fatmucket (L. hydiana), which reaches sexual
maturity around 36 mm (1.4 in) (Howells 2000b, pp. 35-48; Howells
2010c, p. 3). Texas fatmucket females have been found gravid (with
glochidia in the gill pouch) from July through October, although
brooding may continue throughout much of the year (Howells 2010c, p.
3). Texas fatmucket females display a mantle lure to attract host fish,
releasing glochidia when the lure is bitten or struck by the fish.
Bluegill (Lepomis macrochirus) and green sunfish (L. cyanellus) have
been successful hosts in laboratory studies (Howells 1997b, p. 257).
Hosts such as these sunfishes are common, widely distributed species in
Texas that occur in an array of habitat types (Hubbs et al. 2008, p.
45) and would not generally be expected to be a limiting factor in
Texas fatmucket reproduction and distribution (Howells 2010c, p. 3).
Habitat
The Texas fatmucket occurs in moderately sized rivers in mud, sand,
or gravel, or mixtures of these substrates (Howells 2010c, p. 4) and
sometimes in narrow crevices between bedrock slabs (Howells 1995, p.
21). Live individuals have been found in relatively shallow water,
rarely more than 1.5 meters (m) (4.9 feet (ft)) deep, and usually less.
Remaining populations typically occur at sites where one or both banks
are relatively low, allowing floodwaters to spread out over land and
thereby reducing damage from scouring (Howells 2010c, p. 4). The
species does not occur in ponds, lakes, or reservoirs, suggesting that
it is intolerant of deep, low-velocity water created by artificial
impoundments.
Distribution and Abundance
Historical Distribution
The Texas fatmucket historically had populations in at least 18
rivers in the upper Colorado, Guadalupe, and San Antonio River systems
in the Texas Hill Country and east-central Edwards Plateau region of
central Texas. In the Colorado River, it ranged from Travis County
upstream approximately 320 kilometers (km) (200 miles (mi)) to Runnels
County in the Colorado River. It was also found in many tributaries,
including the Pedernales, Llano, San Saba, and Concho Rivers, and Jim
Ned, Elm, and Onion Creeks (Howells et al. 1996, p. 61).
In the Guadalupe-San Antonio River basin, the Texas fatmucket
occupied approximately 240 km (150 mi) of the Guadalupe River, from
Gonzales County upstream to Kerr County, including the North Guadalupe
River, Johnson Creek, and the Blanco River. In the San Antonio River,
it ranged from its confluence with the Medina River in Bexar County
upstream to the City of San Antonio, as well as in the Medina River and
Cibolo Creek (Howells et al. 1996, p. 61; Howells 2010c, p. 6).
Strecker (1931, pp. 66-68) reported Texas fatmucket from a lake in
Victoria County in the lower Guadalupe River drainage (Howells 2010c,
p. 6), but this is probably a misidentified Louisiana fatmucket, which
occurs in lakes or impoundments. A Salado Creek record from Bell County
(Strecker 1931, pp. 62-63) is also probably a misidentified Louisiana
fatmucket, since the Texas fatmucket is not known to occur in the
Brazos River basin or its western tributaries (Howells et al. 1996, p.
61; Howells 2010c, p. 6).
Current Distribution
Based on historical and current data, the Texas fatmucket has
declined significantly rangewide and is now known from only nine
streams in the Colorado and Guadalupe River systems in very limited
numbers. All existing populations are represented by only one or two
individuals and are likely not stable or recruiting (juvenile mussels
joining the adult population). In the streams where the species is
extant (surviving), populations are highly fragmented and restricted to
short reaches with few exceptions. The Texas fatmucket has been
considered a species of special concern by some malacologists for
several decades (Athearn 1970, p. 28).
Colorado River System
The Texas fatmucket was historically known to occur throughout the
Colorado River and numerous tributaries (Randklev et al. 2010c, p. 4).
However, in the mainstem Colorado River, the Texas fatmucket has not
been found, live or dead, in several decades despite numerous surveys
(Howells 1994, p. 4; 1995, pp. 20-21, 25, 29; 1996, pp. 20, 23; 1997a,
pp. 27, 31, 34-35; 1998, p. 10; 1999, p. 18; 2000a, pp. 25-27; 2002a,
pp. 6-7; 2004, pp. 7, 10-11; 2005, p. 6; Johnson 2009, p. 1; Burlakova
and Karatayev 2010a, p. 12), and thus is considered extirpated
(eliminated from) from the Colorado River mainstem. Within this system,
the species is only known from sparse populations in Colorado River
tributaries, including the South Concho River, Spring Creek, Llano
River (including Threadgill Creek), Pedernales River (including Live
Oak Creek), Onion Creek, Jim Ned Creek, Elm Creek, and the San Saba
River.
Evidence of persisting Texas fatmucket populations has been found
in Spring Creek, a tributary to the Middle Concho River, which flows
into the Concho River, a large tributary of the Colorado River.
Historically, Spring Creek harbored Texas fatmucket in Irion and Tom
Green Counties (Randklev et al. 2010c, p. 1). In 1993, discovery of
shell material prompted additional surveys, and in 1997, one live
individual was found in Irion County (Howells 1998, p. 13). Farther
downstream, in Tom Green County, two live individuals were recorded in
1997, upstream of Twin Buttes Reservoir (Howells 1998, pp. 13-14), but
no evidence of this population was found in 2008 (Burlakova and
Karatayev 2010a, p. 12). Spring Creek was reported to have dried in
1999 and 2000, which may have eliminated the population there (Howells
et al. 2003, p. 5).
In the Llano River, there are three areas that are currently known
to contain Texas fatmucket populations. The species occurred throughout
the length of the river historically (Ohio State University Museum
(OSUM) 2011a, p. 1). A single shell was collected in Llano County in
1992 (Howells 1994, p. 6), and eight live individuals were found in
2011 (Burlakova and Karatayev 2011, p. 1). Individuals were small in
size, indicating a potentially reproducing population. The species also
persists in Mason County, where two shell fragments of recently dead
Texas fatmucket were found in 1995 (Howells 1996, p. 22), and two live
individuals were collected at the same site in 2009 (Burlakova and
Karatayev 2010a, pp. 12-13). The species also appears to persist in
Kimble County, where one live Texas fatmucket was recorded in 2009
(Burlakova and Karatayev 2010a, pp. 12-13).
In 2004, four live Texas fatmucket were recorded from Threadgill
Creek, a tributary to the Llano River in Gillespie and Mason Counties
(Howells 2005, pp. 6-7). This population is on private land, which
limits survey access, but Howells (2009, p. 5) indicates it likely
persists due to favorable land management.
Live Oak Creek, a tributary to the Pedernales River in Gillespie
County, also contains a sparse Texas fatmucket population. In 2002, 11
shells were discovered, and in 2003, one live individual was recorded,
confirming the species persisted in low numbers (Howells 2003, p. 10;
Howells 2004, pp. 8-9). Since that time, surveys have been
[[Page 62169]]
conducted in Live Oak Creek on a fairly regular basis. The stream was
visited in two different occasions in 2004, with only shell material
found (Howells 2005, pp. 7-8), and again in 2005, when two live
individuals were recorded (Burlakova and Karatayev 2010a, p. 12). The
stream was surveyed in 2007 and 2008, but no evidence of the species
was found (Howells 2009, p. 5). This population is presumed to be small
but persisting.
Original records of speckled pocketbook (Lampsilis streckeri) from
Onion Creek in Travis County in 1931 are now believed to have been
misidentified; instead they represent records of Texas fatmucket
(Howells 2010c, p. 6; Randklev et al. 2010c, p. 4). The stream was
surveyed in 1993, and no live freshwater mussels were found (Howells
1995, p. 28). However, in 2010, several live Texas fatmucket were found
during a survey near Highway 71 (Groce 2011, pers. comm.), indicating
the species persists there.
Elm Creek, a tributary to the Colorado River, has been known to
harbor a Texas fatmucket population since 1993, when 10 live
individuals were recorded (Howells 1995, p. 21). Since that time, the
population has declined, with two individuals found in 1995 (Howells
1996, pp. 19-20), and no live individuals found in 2001 or 2005
(Howells 2002a, p. 5; 2006, p. 63). In 2008, additional sites
downstream of the known population were surveyed and one live
individual was recorded after 15 person-hours of searching (Burlakova
and Karatayev 2010a, p. 12), indicating that the species continues to
persist in Elm Creek, although in very low numbers.
Texas fatmucket also persist in the San Saba River, where the
species has been known to occur historically (Randklev et al. 2010c, p.
2; OSUM 2011a, p. 1). The river was surveyed in 1997, and three live
individuals were found (Howells 1998, p. 16). In 2000 and 2004, no
Texas fatmucket were found in this stretch of river (Howells 2001, p.
29; Howells 2005, pp. 8-9). One live individual was found in 2005
(Howells 2006, p. 64), and, in 2008, only one shell of a recently dead
individual was found (Burlakova and Karatayev 2010a, p. 12). In 2005,
the number of mussels of all species collected was about 40 percent of
the 1997 numbers (Howells 2006, p. 64), indicating an overall decline
in the freshwater mussel fauna. Aquatic macrophyte (aquatic plants
larger than algae) abundance has increased in this river, confounding
survey efforts and degrading mussel habitat (Howells 2006, p, 64).
Texas fatmucket have not been found alive in the Pedernales River
since 1978 (Howells 1999, p. 16). In 1992, a thorough search of the
habitat yielded no live Texas fatmuckets, with only very old dead shell
material collected in the banks above the normal high water line
(Howells 1994, p. 4). Because the species was documented from Blanco
County by museum records (OSUM 2011a, p. 1), additional sections of the
river were also surveyed in 1992, with no evidence of Texas fatmucket
found, although in 1993, very old Texas fatmucket shell fragments were
discovered in Pedernales Falls State Park (Howells 1995, p. 28). Mussel
habitat in this area is poor, and it is unlikely the species persists
there. Subsequent searches of the river in 1998 yielded only dead shell
material (Howells 1999, p. 16).
The Texas fatmucket is considered extirpated from the South Concho
River and Jim Ned Creek. In the South Concho River, old Texas fatmucket
shell fragments were found in gravel bars in Tom Green County in 1997,
but there has been no additional evidence of the species (Howells 1998,
p. 12). Additionally, three live individuals were recorded from Jim Ned
Creek in Brown County in 1979 (Randklev et al. 2010c, p. 3), but the
species has not been found in this stream since then (Howells 1997a,
pp. 29-30).
Guadalupe River System
While the Texas fatmucket was never widely distributed in the
Guadalupe River system, the only remaining populations are in the
mainstem Guadalupe River and possibly the North Fork Guadalupe River.
It is presumed extirpated from the entire San Antonio River system, as
well as the Blanco River and Johnson Creek.
In the mainstem Guadalupe River, Texas fatmucket historically
occurred in Kerr County (OSUM 2011a, p. 1). In 1992 and 1995, surveys
yielded no evidence of the species (Howells 1994, pp. 7-8; Howells
1996, p. 25), although shell fragments collected in 1993 in Guadalupe
County may have been Texas fatmucket but were too weathered for an
accurate determination (Howells 1995, p. 31). In 1996, two live
individuals were recorded in Kerr County directly below a dam (Howells
1997a, p. 36), and in 1997, three shells were found at the same site
following a flood (Howells 1998, p. 18). No Texas fatmucket or other
freshwater mussels have been found at that site since, and it is
unlikely that Texas fatmucket persist there (Howells 2006, p. 71).
However, 20 recently dead individuals were discovered approximately 1
km (0.6 mi) downstream in Louise Hayes Park during a drawdown (Howells
1999, pp. 18-19), and 6 live individuals were found at the same
location in 2005 (Howells 2006, pp. 71-72). Surveys in 2007 and 2008
yielded no live or recently dead individuals (Burlakova and Karatayev
2010a, p. 12). It is likely that the species persists in the vicinity.
There has been no other evidence of Texas fatmucket in the mainstem
Guadalupe River in recent years.
In 1999, two recently dead Texas fatmucket were found in North Fork
Guadalupe River (Howells 2000a, p. 27). This river was surveyed again
in 2000 and 2003 at several sites, and no Texas fatmucket were found
(Howells 2001, p. 31; Howells 2004, pp. 13-14).
Johnson Creek was a historical location for Texas fatmucket, but no
live freshwater mussels of any species have been found in this stream
for decades (Howells 1996, p. 25; Howells 1998, p. 18; Howells 2002a,
p. 8). Additionally, the Blanco River has been surveyed extensively
since 1992, and no evidence of Texas fatmucket has been collected, nor
is suitable habitat present (Howells 1994, p. 9; Howells 1995, pp. 32-
33; Howells 1996, p. 28; Johnson 2011, p. 1). The last collection of
Texas fatmucket from the Blanco River occurred in the 1970s or 1980s
(Howells 2005, p. 10).
Texas fatmucket have also been extirpated from the entire San
Antonio River system. The mainstem San Antonio River was surveyed in
1993 and 1996, and no live or dead Texas fatmucket were found (Howells
1995, p. 35; 1997a, pp. 41-42). It was known from the Medina River, a
tributary to the San Antonio River, historically (Randklev et al.
2010c, p. 3), but no mussels of any species have been found in this
river in recent years (May 2011, pers. comm.). Additionally, although
Texas fatmucket were collected from Cibolo Creek historically (OSUM
2011a, p. 1) and shell material, likely from Texas fatmucket, was found
in 1993 (Howells 1995, p. 36), no live freshwater mussels have been
found in Cibolo Creek since (Howells 1997a, pp. 40-41).
Summary
Based on historical and current data, the Texas fatmucket has
declined significantly rangewide and has been extirpated from most of
the Guadalupe River system and hundreds of miles of the Colorado River,
as well as from numerous tributaries. Extant populations are
represented by only a few individuals, and they are highly disjunct and
restricted to short reaches. Two of the populations considered extant
in recent years may now be
[[Page 62170]]
extirpated, and the remaining seven populations are extremely small and
likely not stable. No evidence of recent recruitment has been found in
any of the populations, with the possible exception of the Llano River.
Species Information for Golden Orb
Species Description
The golden orb is small, usually less than 82 mm (3.2 in), with an
oval to nearly round, smooth, and unsculptured shell, except for
concentric growth rings (Howells 2002b, p. 6). External shell
coloration varies from yellow-brown, gold, or orangish-brown to dark
brown or black, and some individuals may show faint greenish rays.
Internally, the nacre is white to bluish-white (Howells 2002b, p. 6).
Taxonomy
The golden orb was originally described as Unio aureas by Lea in
1859 and later moved to the genus Quadrula in 1900 (Simpson 1900, p.
783). Graf and Cummings (2007, p. 18) have proposed moving it to the
genus Amphinaias, but other freshwater mussel taxonomists recommend
waiting for additional work to be completed on members of Quadrula
before splitting the genus (Bogan 2011, pers. comm.). Because the
golden orb can exhibit an elongated shell structure in headwater
riffles, old records of Unio bolli in the Colorado River (Dall 1882, p.
956) are very likely elongated forms of golden orb (Howells 2010a, p.
5). The golden orb is recognized by the Committee on Scientific and
Vernacular Names of Mollusks of the Council of Systematic
Malacologists, American Malacological Union (Turgeon et al. 1998, p
36), and we recognize it as a valid species.
Biology and Life History
There is no specific information on age, size of maturity, or host
fish use for golden orb. Other species in the genus Quadrula
successfully parasitize catfish, and it is likely golden orb do as well
(Howells 2010a, p. 3). Gravid females have been found from May through
August (Howells 2000b, p. 38). Mussels in the genus Quadrula are short-
term brooders, which are species that hold fertilized eggs and
glochidia for a short period, usually 3 to 6 weeks, before releasing
glochidia (Gorden and Layzer 1989, p. 6; Garner et al. 1999, p. 277).
Habitat
The golden orb has been found almost exclusively in flowing waters
in moderately sized rivers (Howells 2010a, p. 3). It has been found in
only one reservoir in the lower Nueces River (Lake Corpus Christi),
where wave action may simulate flowing water conditions (Howells 2010a,
p. 3). This species is found in substrates of firm mud, sand, and
gravel, and it does not appear to tolerate more unstable substrates
such as loose sand or silt (Howells 2002b, p. 6).
Distribution and Abundance
Historical Distribution
The golden orb is endemic (native) to nearly the entire lengths of
the Guadalupe, San Antonio, and Nueces-Frio River basins in central
Texas (Howells 2010a, p. 5), including the Guadalupe, Medina, San
Antonio, Frio, and Nueces Rivers and Cibolo Creek. It was originally
reported from four sites in the Brazos River system (Strecker 1931, p.
63), but these are almost certainly misidentified smooth pimpleback
(Howells 2002b, p. 5) based on numerous mussel surveys throughout the
Brazos River system since the 1970s that failed to find any golden orb.
The species has not been found in studies of archaeological specimens
from the Brazos River (Howells 2010a, p. 5), further indicating golden
orb did not historically occur in the Brazos River system.
The golden orb has also been reported from the upper Colorado River
drainage (Howells et al. 1996, pp. 108-109; Randklev et al. 2010c, p.
4), but these appear to have been misidentified Texas pimpleback
(Howells 2010a, p. 5). Since no other golden orb have been reported
from the Colorado River system, we do not believe it occurred in that
basin.
Current Distribution
Based on historical and current data, the golden orb has declined
significantly rangewide and is now known from only four streams in
disjunct locations. Despite mussel surveys across the historical range,
since 1995 golden orb has only been found in Lake Corpus Christi and
the Guadalupe, lower San Marcos, and lower San Antonio Rivers. The
species has been extirpated from the entire Nueces-Frio River basin,
except at the extreme downstream end of the Nueces River, where a
population persists in Lake Corpus Christi. Aside from the upper
Guadalupe River, all existing populations occur in the lower portion of
occupied basins in a small geographical area; only about 130 km (80 mi)
separate the farthest two populations. Only four populations appear to
be relatively stable and recruiting, while the remaining five
populations are represented by only a few individuals.
Guadalupe River System
In the Guadalupe River system, the golden orb historically ranged
throughout the length of the Guadalupe, San Antonio, and San Marcos
Rivers. Currently in this basin, the species only persists in the
uppermost Guadalupe River and lower San Marcos, San Antonio, and
Guadalupe Rivers. The lower portion of this basin (within approximately
120 km (75 mi) of the Gulf of Mexico) harbors all four of the large,
presumably reproducing populations of golden orb.
Historically known from the mainstem Guadalupe River (Howells
2002a, p. 8), the golden orb was not seen in the upper Guadalupe River
in Kerr County again, despite repeated surveys (Howells 1994, pp. 7-8;
1996, p. 30; 1997a, p. 36), until 1997, when three shells were
discovered (Howells 1998, p. 18). No live freshwater mussels of any
species have been found in this area, just downstream of a dam, since
1997 (Howells 1999, p. 18; Howells 2006, p. 71), and it is unlikely
golden orb persists there. However, upstream of this area, above the
dam and impounded reach, a single recently dead individual was found in
1998 during an extended drawdown of the river to construct a footbridge
in a local park (Howells 1999, pp. 18-19). In 2005, two live
individuals were also found at this site (Howells 2006, pp. 71-72),
showing that the species had survived the drawdown and persists at the
site.
Golden orb also occurs farther downstream in the mainstem Guadalupe
River, near Lake Gonzales in Gonzales County. Upstream of the
reservoir, subfossil shells (very old shells that are brittle,
crumbling, and with extensive erosion) were found in 1993 (Howells
1995, p. 31), but the species has not been found there since. However,
below the reservoir, one recently dead individual was collected in 1995
(Howells 1996, pp. 26-27), and in 1996, 25 live golden orb were
recorded at two sites in this area (Howells 1997a, pp. 37-38). Later,
in 2006, three live golden orb were also found in this area (Howells
2006, pp. 85-86). A small population apparently continues to persist
below Lake Gonzales.
A large golden orb population occurs farther downstream in the
mainstem Guadalupe River, below Lake Wood, also in Gonzales County.
Although none were found during a survey in 1995 (Howells 1996, p. 27),
36 live golden orb were found at two sites below Lake Wood in 1996
(Howells 1997a, pp. 38-40). Density estimates were calculated based on
the quantitative information collected from these surveys, but they
[[Page 62171]]
were not considered statistically valid (Howells 1997a, p. 40) and so
are not reported here. Only one live golden orb was found at this site
in 2002 (Howells 2003, p. 11), but a relatively large population
continues to persist; a total of around 100 live golden orb were found
at three sites within 2 km (1.2 mi) of the Lake Wood Dam in 2006
(Howells 1996, pp. 87-91). Also, in 2008, 33 golden orb were recorded
alive downstream of Lake Wood (Burlakova and Karatayev 2010a, p. 14).
This portion of the Guadalupe River supports a relatively large
population of golden orb, and it also contains one of the most abundant
freshwater mussel communities in Texas (Burlakova and Karatayev 2010a,
p. 14).
In 2009, a large population of golden orb was discovered farther
downstream in the mainstem Guadalupe River in Victoria County, when
over 100 individuals were found (Johnson 2009, p. 1). Multiple size
classes were observed, including juveniles, indicating this population
is reproducing and recruiting new individuals into the population. A
large number of shells was collected upstream of this site in 1994
(Burlakova and Karatayev 2010c, p.1), but no golden orb were seen alive
until 2009.
The San Marcos River, a tributary to the Guadalupe River, also
supports a large golden orb population near its confluence with the
tailwaters (outflow) of Lake Wood Dam. Although much of the San Marcos
River has been extensively surveyed, with very few freshwater mussels
present of any species (Howells 1995, pp. 33-34; 1997a, p. 40; 2004,
pp. 15-16, 18; 2005, p. 10), one old golden orb shell was found near
the town of Staples (Howells 1998, p. 19), and a single live individual
was found near the town of Luling (Howells 1999, p. 28). Downstream
from these locations, a large population persists in the vicinity of
Palmetto State Park in Gonzales County. In 1995, a recently dead
individual was discovered downstream of the park, indicating the recent
presence of the species (Howells 1996, p. 28), and, based on surveys
from 2000-2006, a relatively large population was confirmed to be in
the area (Howells 2001, pp. 32-33; 2006, pp. 72-73; 2006, p. 91;
Burlakova and Karatayev 2010a, pp. 14-15).
Historically, golden orb were numerous in the San Antonio River in
Karnes County (OSUM 2011b, p. 1), but only a single subfossil shell was
found at each of two sites in Karnes County in 1996 (Howells 1997a, pp.
41-42). No live animals have been found there since, although abundant
shell material remains present (Karatayev and Burlakova 2008, p. 40).
The lower portion of the San Antonio River supports the largest
known golden orb population. In 2007, 37 live golden orb were recorded
near Goliad in Goliad County, both within and downstream of Goliad
State Park (Howells 2009, p. 11). The following year, 285 live golden
orb were found within the park and downstream surrounded by private
lands (Burlakova and Karatayev 2010a, p. 15). This site represents the
largest known population of golden orb.
In 2009, a single live golden orb was discovered in the lower San
Antonio River south-southwest of Victoria in Victoria County (Johnson
2009, p. 1); this site has not been surveyed since. We presume golden
orb may persist in this stretch of river.
The golden orb appears to have been extirpated from the Medina
River. The species historically occurred in Medina and Bexar Counties
(Randklev et al. 2010b, p. 4; OSUM 2011b, p. 1), but no live or dead
mussels of any species have been found in this river in recent years
(May 2011, pers. comm.).
Cibolo Creek, a tributary to the San Antonio River, was extensively
surveyed in the 1990s, with only old golden orb shells collected in
Wilson County (Howells 1995, pp. 35-37; 1997a, pp. 40-41). In 2006 and
2007, Burlakova and Karatayev (2010b, p. 1) surveyed this same general
area and found only shell material. It is unlikely golden orb remain in
Cibolo Creek.
Nueces-Frio River System
Information is limited on the occurrence of golden orb in the
Nueces River. Other than a population that occurs in a reservoir on the
lower Nueces River (Lake Corpus Christi), the species appears to be
extirpated from the remainder of the basin.
Historically, the golden orb occurred in the Nueces River in Live
Oak County (OSUM 2011b, p. 1). It was last seen alive in the Nueces
River in 1993, when unreported numbers were found in the same area
(Burlakova and Karatayev 2010c, p. 1). A shell was collected in the
same general area in 1995 (Burlakova and Karatayev 2010c, p. 1), but
additional surveys in 1996 and 1997 found no evidence of the species
(Howells 1997a, pp. 43-44; 1998, p. 20). We presume the species no
longer occurs in the upper portions of the Nueces River.
An anomalous (odd) population of golden orb has persisted in Lake
Corpus Christi Reservoir in the lower Nueces River. While the species
does not typically inhabit lentic (ponded) water, wave action is
presumed to simulate flowing water conditions and has supported a
golden orb population since at least the 1970s (OSUM 2011b, p. 1). A
few live individuals of golden orb have been found within the reservoir
consistently since 1994 (Howells 1995, p. 39; 1996, pp. 30-31;
Burlakova and Karatayev 2010c, p. 1). Numbers of golden orb collected
increased in 1996, when 86 live golden orb were found at three
different locations within the reservoir (Howells 1996, pp. 30-31).
However, a drawdown of the lake in 1996 resulted in large numbers of
golden orb stranded and killed (Howells 2010a, p. 9), and in 1998 no
live individuals were found (Howells 1999, p. 19). Again in 2005, no
live individuals were found during surveys, but in 2006, a total of
nine were collected at three different sites within the reservoir
(Howells 2006, pp. 73-76, 91-93). A small golden orb population likely
persists in the reservoir.
Very little information is available on the distribution of golden
orb in the Frio River. Shells were last seen in McMullen County in 1994
(Burlakova and Karatayev 2010c, p. 1), but no evidence of the species
has been found in this river since (Howells 1995, pp. 37-38; 1996, p.
29; 2002a, pp. 9-10; 2004, pp. 19-20).
Summary
Based on historical and current data, the golden orb has declined
rangewide and is now known from only nine populations in four rivers
and has been eliminated from nearly the entire Nueces-Frio River
system. Four of these populations appear to be stable and reproducing;
the remaining five populations are small and isolated and show no
evidence of recruitment. Only the populations in the middle Guadalupe
River and lower San Marcos River are likely connected; the remaining
extant populations are highly fragmented and restricted to short
reaches.
Species Information for Smooth Pimpleback
Species Description
The smooth pimpleback is a nearly round, thick-shelled freshwater
mussel that generally reaches at least 60 mm (2.6 in) in length
(Howells 2010b, p. 4). It is moderately thick, solid, and inflated.
Externally, the smooth pimpleback, like its name suggests, is
relatively smooth with minute sculpturing; it may or may not have a few
small pustules (raised bumps) (Howells 2010b, p. 2). The external
coloration of the shell ranges from tan
[[Page 62172]]
to light brown, dark brown, and black with no rays (Howells 2010b, p.
4).
Taxonomy
The smooth pimpleback was originally described by Lea in 1859 as
Unio houstonensis. It was later placed in the genus Margaron and
ultimately moved to Quadrula by Simpson (1900, p. 782). Graf and
Cummings (2007, p. 18) have proposed moving it to the genus Amphinaias,
but other freshwater mussel taxonomists recommend waiting for
additional work to be completed on members of Quadrula before splitting
the genus (Bogan 2011, pers. comm.). The smooth pimpleback is
recognized by the Committee on Scientific and Vernacular Names of
Mollusks of the Council of Systematic Malacologists, American
Malacological Union (Turgeon et al. 1998, p 37), and we recognize it as
a valid species.
Biology and Life History
There is no specific information on age, size of maturity, or host
fish use for smooth pimpleback. Numerous individuals were examined for
gravidity between June and November, with no evidence of eggs or
glochidia (Howells 2000b, p. 38). Other species in the genus Quadrula
successfully parasitize catfish, and it is likely smooth pimpleback
does as well (Howells 2010b, p. 2); additionally, mussels in the genus
Quadrula are typically short-term brooders (Gorden and Layzer 1989, p.
6; Garner et al. 1999, p. 277), and we expect the same of the smooth
pimpleback.
Habitat
The smooth pimpleback has been found in mud, sand, and fine gravel
in medium-to-large rivers and some reservoirs (Howells 2010b, p. 3).
Unlike most other Quadrula species in central Texas, smooth pimpleback
do occur in some reservoirs (Howells 2002b, p. 8; 2010b, p. 3).
Distribution and Abundance
Historical Distribution
The smooth pimpleback is native to the central and lower Brazos and
Colorado Rivers and their tributaries in central Texas (Howells 2010b,
p. 4). The smooth pimpleback has also been reported from the Trinity
River and other drainages in Texas, as well as from areas outside of
Texas, including southern Arkansas and the Verdigris River in Kansas.
These reports are likely misidentifications of other pimpleback species
that can sometimes closely resemble smooth pimpleback (Howells 2010b,
pp. 4-5). The smooth pimpleback was historically uncommon where it
occurred; from the 1960s through the 1990s, experts failed to find
large populations persisting throughout its range (Howells 2009, p.
12).
In the Colorado River, historical reports indicate that the smooth
pimpleback occurred from San Saba County downstream to Wharton County,
as well as in the Llano River and Onion and Skull Creeks. Within the
Brazos River basin, the species historically occurred throughout the
length of the mainstem of the Brazos River (Howells 2009, p. 12), as
well as in the Clear Fork Brazos, Leon, Navasota, Little Brazos, San
Gabriel, Lampasas, and Little Rivers and Yegua Creek (Howells 2010b,
pp. 4-6; Randklev et al. 2010b, p. 20).
Current Distribution
The smooth pimpleback has been nearly extirpated from the Colorado
River basin, and a few small populations persist in the Brazos River
basin. Recent surveys suggest a greater abundance and distribution of
the smooth pimpleback in the central Brazos River drainage than was
indicated by collections from the past 40 years, with five populations
represented by more than a few individuals.
Colorado River System
The smooth pimpleback historically occurred throughout the mainstem
Colorado River as well as several tributaries, but it is currently
restricted to one mainstem reservoir, two sites on the mainstem
Colorado River, and the San Saba River. Populations in all of the other
historically occupied tributaries and two reservoirs appear to have
been extirpated.
In the mainstem Colorado River, smooth pimpleback were historically
known from much of the length of the river (Howells 1996, p. 21; 1997a,
pp. 34-35; Randklev et al. 2010c, p. 4; OSUM 2011c, p. 1). Numerous
surveys in many locations on the Colorado River occurred between 1993
and 2009, and no evidence of smooth pimpleback was found (Howells 1995,
p. 29; 1996, p. 23; 1997a, pp. 27, 31; 2002a, p. 6; 2004, p. 7, 11;
2005, p. 6; Burlakova and Karatayev 2010a, pp. 15-16), except for in
Colorado County in 1999, when three live smooth pimpleback were found
(Howells 2000a, p. 27). During two surveys in 2009, live smooth
pimpleback were found in the same general area as in 1999 (Burlakova
and Karatayev 2010a, p. 16; Johnson 2009, p. 1). Farther downstream, in
Wharton County, live smooth pimpleback were found at two sites in 2009
(Burlakova and Karatayev 2010a, p. 16), despite having been surveyed in
1995 and none found (Howells 1996, p. 23).
Inks Lake is a small mainstem reservoir on the Colorado River in
Burnet County. Several live smooth pimpleback were found in 1992
(Howells 1994, p. 4); however, since that time only shell material has
been found during four separate surveys between 1996 and 2005 (Howells
1997a, pp. 32-33; 1999, p. 16; 2005, p. 8; 2006, p. 67). Frequent
drawdowns in this lake appear to have affected all species of
freshwater mussels, as there has been a sharp decline in the overall
mussel community (Howells 1999, p. 16).
One live smooth pimpleback was found in Lake Lyndon B. Johnson, a
large mainstem reservoir on the Colorado River, in 2001, but no live
individuals have been found since (Howells 2002a, pp. 6-7; 2006, pp.
68-69). Farther downstream, in Lake Marble Falls, 13 live smooth
pimpleback were found in 1995 during a drawdown of lake levels (Howells
1996, p. 22), but subsequent surveys in 1996 failed to find any
additional living animals (Howells 1997a, p. 33). The small recent
survey effort is not sufficient to conclude that the smooth pimpleback
no longer occur in these lakes, and small populations may still persist
there.
Smooth pimpleback were recently found in the San Saba River in San
Saba County, when 29 individuals were found at two locations (Burlakova
and Karatayev 2011, p. 5). Various size and age classes were
represented, indicating a reproducing, recruiting population (Burlakova
and Karatayev 2011, p. 5). Even more recently, 206 smooth pimpleback,
including adults and juveniles, were recorded in this same area in
riffle and pool habitat (Randklev 2011b, p. 1).
No smooth pimpleback populations remain in any of the Colorado
River tributaries in which the species was historically known to occur,
including the full length of the Llano River (Howells 1996, pp. 21-22;
1998, p. 17; 2000a, p. 25; 2005, p. 8; Randklev et al. 2010c, p. 4;
OSUM 2011c, p. 1). A single subfossil shell, likely a smooth
pimpleback, was found in the Llano River in Kimble County in 1995
(Howells 1996, pp. 21-22), but no other evidence of the species has
been found in the Llano River in recent years. Additionally, although
Onion and Skull Creeks were historically occupied by smooth pimpleback
(Randklev et al. 2010c, p. 4), the species has not been found recently
in either stream (Howells 1995, pp. 28-29).
[[Page 62173]]
Brazos River System
The smooth pimpleback historically occurred in the Brazos River
system from Palo Pinto County downstream to Austin and Waller Counties,
as well as in numerous tributaries. The species has been extirpated
from the upstream half of the mainstem Brazos River and from at least
three tributaries. Substantial populations persist in the Leon River,
Navasota River, and Yegua Creek, and small populations remain in the
lower Brazos and Little Brazos Rivers.
In the mainstem Brazos River, surveys in Palo Pinto, Somervell, and
Bosque Counties between 1996 and 2000 indicate that the smooth
pimpleback has been extirpated from the upstream portion of the river
(Howells 1997a, pp. 16, 18-19; 1999, pp. 11-12; 2001, p. 19). Despite
surveys in 1996 and 1998 in which no individuals were found (Howells
1997a, p. 21; 1999, p. 12), a single live smooth pimpleback was found
in McLennan County in the middle Brazos River in 2005 (Howells 2010b,
p. 5), and two live individuals were recorded in Falls County in 2006
(Karatayev and Burlakova 2008, pp. 6-10).
Although not extirpated from the middle Brazos River, the smooth
pimpleback occurs only in low numbers. In Milam and Robertson Counties,
no smooth pimpleback were found in 1998 (Howells 1999, p. 13), but
eight live individuals were found in 2006 (Burlakova and Karatayev
2010b, p. 1). More recently, in 2008, 13 live smooth pimpleback were
found at the same site (Randklev et al. 2009, p. 18). Additionally,
downstream in Burleson and Brazos Counties, which were historically
occupied by the smooth pimpleback (OSUM 2011c, p. 1), a small
population persists. In 1995, one live and one recently dead individual
were collected within Brazos County (Howells 1996, pp. 17-18). Although
none were found here in 1999 (Howells 2000a, pp. 21-22), in 2006 a
single live smooth pimpleback was collected at this site (Karatayev and
Burlakova 2008, pp. 6-10). Additionally, further downstream in Grimes
and Waller Counties, a single live individual was found in 2006
(Burlakova and Karatayev 2010b, p. 1) and again in 2008 (Randklev et
al. 2009, p. 18). Smooth pimpleback are more numerous in the lower
mainstem Brazos River, in Austin and Waller Counties, where 38 live
individuals were found in 2006 (Karatayev and Burlakova 2008, pp. 6-
10).
Tributaries to the Brazos River also contain smooth pimpleback
populations. The Leon River, in the Little River drainage of the
Brazos, historically contained smooth pimpleback throughout its length
in Hamilton, Coryell, and Bell Counties (Howells 1994, p. 19, 1997a, p.
20; Randklev et al. 2010c, p. 4; OSUM 2011c, p. 1). Currently, a smooth
pimpleback population persists in Hamilton County, where numerous live
individuals were found in 2006 and 2011 (Howells 2006, pp. 82-83;
Randklev 2011a, p. 1), as well as several locations in Coryell County,
where numerous individuals were also recently found (Randklev 2011a, p.
1).
Only subfossil smooth pimpleback shells have been found in the
Lampasas River in Bell County in 1996 (Howells 1997a, pp. 20, 23).
Subsequent surveys of the river in both Bell and Lampasas Counties
yielded no evidence of smooth pimpleback (Howells 1999, p.14; 2001, p.
20), and the species has likely been extirpated from the Lampasas
River.
The Little River in Milam County is also a historical location for
the smooth pimpleback (Randklev et al. 2010c, p. 4). Old shells were
found at this site in 1996 (Howells 1997a, p. 22), and a single live
individual was found here in 2006 (Karatayev and Burlakova 2008, p. 6).
Farther downstream, at the confluence with the Brazos River, none have
been found (Howells 1996, p. 17).
A single old smooth pimpleback shell has been found in the San
Gabriel River in Milam County (Howells 1997a, p. 23), and it is likely
the species has been extirpated from this Brazos River tributary as
well.
In the Little Brazos River, the smooth pimpleback appears to
persist in low numbers. Although none were found in Robertson County in
1993 and there had appeared to be a die off of numerous freshwater
mussel species (Howells 1995, p. 18), one live smooth pimpleback was
found during a 2006 survey (Karatayev and Burlakova 2008, p. 6).
Farther downstream in Brazos County, recently dead individuals were
discovered in 2001 (Howells 2002a, pp. 4-5). The species occurred in
this area historically (Randklev et al. 2010c, p. 4), and reports of
mussels in the Little Brazos River from the 1950s described the
freshwater mussel community as numerous, including smooth pimpleback
(Gentner and Hopkins 1966, pp. 458-459), but no live individuals have
been collected in this area in recent years (Howells 1996, p. 18; 1999,
p. 14).
The smooth pimpleback has been extirpated from the Clear Fork
Brazos River. Although this species was originally documented from this
river in Shackelford County in 1893 (Randklev et al. 2010c, p. 4), none
have been found in this stream since (Howells 1999, p. 19).
In the Navasota River, smooth pimpleback historically occurred in
Leon, Brazos, Grimes, and Washington Counties (Randklev et al. 2010c,
p. 4; OSUM 2011c, p. 1). Currently, the species persists in each of
those counties, with a large population occurring in the lower river.
In Leon County three recently dead smooth pimpleback shells were found
in 2000 (Howells 2001, p. 23), indicating that a few individuals may
persist in the area. However, one of the largest known populations
occurs farther downstream near the confluence of the Navasota and
Brazos Rivers. Nine live individuals were found in this area in 2006
(Karatayev and Burlakova 2008, pp. 6-10), and in 2008 a total of 117
live smooth pimpleback were recorded at 3 different locations within
Washington and Grimes Counties (Randklev et al. 2009, pp. 6, 18). A
large population continues to persist in the Navasota River, with a
total of 314 smooth pimpleback recorded at two sites in 2011 (Randklev
2011a, p. 1).
In Yegua Creek, no smooth pimpleback were found during several
surveys between 1996 and 2003 (Howells 1997a, pp. 24-26; 2001, p. 22;
2004, p. 6), although subfossil shells were found in Washington County
in 1996. However, in 2006, a live individual was discovered (Karatayev
and Burlakova 2008, pp. 6-10), which prompted further surveys in 2008.
Numerous smooth pimpleback were found during subsequent surveys at four
different locations within Washington and Burleson Counties (Randklev
et al. 2009, pp. 16-18; Randklev 2011a, p. 1), indicating the presence
of a potentially large population in this stream.
Summary
Based on historical and current data, the smooth pimpleback has
declined rangewide and is now known from only nine locations. The
species has been eliminated from nearly the entire Colorado River and
all but one of its tributaries, as well as from the upper Brazos River
and several tributaries. The San Saba River, lower Brazos River,
Navasota River, Leon River, and Yegua Creek populations appear to be
stable and reproducing, but the remaining populations are small,
isolated, and represented by only a few individuals.
Species Information for Texas Pimpleback
Species Description
The Texas pimpleback is a large pimpleback species with a
moderately
[[Page 62174]]
inflated shell that generally reaches 60-90 mm (2.4-3.5 in) (Howells
2002b, pp. 3-4). With the exception of growth lines, the shell of the
Texas pimpleback is generally smooth and moderately thick (Howells
2002b, p. 4). Externally, coloration ranges from yellowish-tan to dark
brown with some individuals mottled or with dark green rays.
Internally, the nacre is white and iridescent posteriorly (Howells
2002b, p. 4).
Taxonomy
The Texas pimpleback was originally described as Unio petrinus by
Gould in 1855. It was placed in the genus Margaron by Lea in 1870 and
ultimately moved to Quadrula by Simpson in 1900 (Simpson 1900, p. 783).
Graf and Cummings (2007, p. 18) have proposed moving it to the genus
Amphinaias, but other freshwater mussel taxonomists recommend waiting
for additional work to be completed on members of Quadrula before
splitting the genus (Bogan 2011, pers. comm.). The Texas pimpleback is
recognized by the Committee on Scientific and Vernacular Names of
Mollusks of the Council of Systematic Malacologists, American
Malacological Union (Turgeon et al. 1998, p. 37), and we recognize it
as a valid species.
Biology and Life History
There is very little specific information on age, size of maturity,
or host fish use for Texas pimpleback. Gravid females have been found
from June through August, and the smallest documented gravid female was
45 mm (1.8 in) long (Howells 2000b, p. 38). Glochidia are hookless and
elliptical in shape (Howells et al. 1996, p. 120). To date, no host
fish have been confirmed for the Texas pimpleback; however, glochidia
have been reported attached to and encysted on flathead catfish
(Pylodictis olivaris), yellow bullhead (Ameiurus natalis), and bluegill
in laboratory settings, although none transformed to the juvenile stage
(Howells 2010e, p. 3). This is consistent with other species in the
genus Quadrula, which also parasitize catfish species.
Habitat
The Texas pimpleback typically occurs in moderately sized rivers,
usually in mud, sand, gravel, and cobble, and occasionally in gravel-
filled cracks in bedrock slab bottoms (Horne and McIntosh 1979, p. 122;
Howells 2002b, p. 4). The species has not been found in water depths
over 2 m (6.6 ft). Texas pimpleback have not been found in reservoirs,
which indicates that this species is intolerant of deep, low-velocity
waters created by artificial impoundments (Howells 2002b, p. 4). In
fact, Texas pimpleback appear to tolerate faster water more than many
other mussel species (Horne and McIntosh 1979, p. 123).
Distribution and Abundance
Historical Distribution
The Texas pimpleback is endemic to the Colorado and Guadalupe-San
Antonio River basins of central Texas (Howells 2002b, p. 3). In the
Colorado River basin, Texas pimpleback occurred throughout nearly the
entire mainstem, as well as numerous tributaries, including the Concho,
North Concho, San Saba, Llano, and Pedernales Rivers, and Elm and Onion
Creeks (Howells 2010e, p. 5; Randklev et al. 2010c, p. 4; OSUM 2011d,
p. 1). Within the Guadalupe-San Antonio River basin, it occurred
throughout most of the length of the Guadalupe River, as well as in the
San Antonio, San Marcos, Blanco, and Medina Rivers (Horne and McIntosh
1979, p. 122; Howells 2010e, p. 5; OSUM 2011d, p. 1).
Current Distribution
The Texas pimpleback has declined significantly rangewide, and only
four streams--the San Saba River, Concho River, Guadalupe River, and
San Marcos River--are known to harbor persisting Texas pimpleback
populations. These populations are disjunct, small, and isolated. The
species has been extirpated from the remainder of its historical range.
Colorado River System
In the Colorado River system, Texas pimpleback once occurred
throughout the mainstem and in many major tributaries. Currently, the
species has been extirpated from the Pedernales, North Concho, and
Llano Rivers, as well as Onion Creek. It has also likely been
extirpated from the mainstem Colorado River and Elm Creek. The Concho
River contains the most abundant population of Texas pimpleback and one
of only two populations of the species likely to be remaining in the
Colorado River system, but most individuals are old and there has been
very little evidence of recruitment.
In the mainstem Colorado River, Texas pimpleback historically
occurred from Runnels County downstream to Colorado County (Howells
2010e, p. 5; Randklev et al. 2010c, pp. 3-4; OSUM 2011d, p. 1).
However, surveys in numerous locations along the river yielded no
evidence of the species anywhere except in Runnels and San Saba
Counties (Howells 1995, pp. 20, 29; 1997a, pp. 27, 31, 35; 2000a, p.
27; 2002a, p. 7). In Runnels County, Texas pimpleback shells were found
in 1993 (Howells 1995, p. 20), but several subsequent surveys between
1996 and 2008 detected no further evidence of the species (Howells
1997a, p. 27; 1998, p. 10; 2002a, p. 7; 2004, p. 7; Burlakova and
Karatayev 2010a, p. 10). In San Saba County, a single shell was
collected in 1989 (Howells 2002b, p. 6), and three recently dead
individuals were found in 1999 (Howells 2000a, pp. 25-26). An
additional shell was collected in 2001 (Howells 2002a, p. 6). No live
individuals have been collected from this reach of the Colorado River.
In Runnels County, Elm Creek once supported a Texas pimpleback
population. Small numbers of Texas pimpleback were found in 1993 and
1995 (Howells 1995, p. 21; 1996, p. 20), but none were found in 1997,
2001, or 2003 (Howells 1998, p. 11; 2002a, p. 5; 2004, p. 7). In 2005
and 2008, only dead individuals were col