Endangered and Threatened Wildlife and Plants; Endangered Status for the Cumberland Darter, Rush Darter, Yellowcheek Darter, Chucky Madtom, and Laurel Dace, 48722-48741 [2011-20018]
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Federal Register / Vol. 76, No. 153 / Tuesday, August 9, 2011 / Rules and Regulations
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92210–0–0008 B2]
RIN 1018–AV85
Endangered and Threatened Wildlife
and Plants; Endangered Status for the
Cumberland Darter, Rush Darter,
Yellowcheek Darter, Chucky Madtom,
and Laurel Dace
Fish and Wildlife Service,
Interior.
ACTION: Final rule.
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AGENCY:
We, the U.S. Fish and
Wildlife Service (Service), determine
endangered status for the Cumberland
darter (Etheostoma susanae), rush darter
(Etheostoma phytophilum), yellowcheek
darter (Etheostoma moorei), chucky
SUMMARY:
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*
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73 FR 25508
75 FR 31702
[Insert FR citation for this Final Rule].
madtom (Noturus crypticus), and laurel
dace (Chrosomus saylori) under the
Endangered Species Act of 1973, as
amended (Act). This final rule
implements the Federal protections
provided by the Act for these species
throughout their ranges, including
Cumberland darter in Kentucky and
Tennessee, rush darter in Alabama,
yellowcheek darter in Arkansas, and
chucky madtom and laurel dace in
Tennessee. We intend to propose
critical habitat in an upcoming
rulemaking, which is expected within
the next few months.
This rule becomes effective
September 8, 2011.
DATES:
This final rule is available
on the Internet at https://
www.regulations.gov at Docket No.
FWS–R4–ES–2010–0027. Comments
and materials received, as well as
supporting documentation used in the
preparation of this rule, will be
ADDRESSES:
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Federal Register / Vol. 76, No. 153 / Tuesday, August 9, 2011 / Rules and Regulations
available for public inspection, by
appointment, during normal business
hours at: U.S. Fish and Wildlife Service,
Tennessee Ecological Services Field
Office, 446 Neal Street, Cookeville, TN
38501; telephone 931–528–6481;
facsimile 931–528–7075.
FOR FURTHER INFORMATION CONTACT: For
information regarding the Cumberland
darter, contact Lee Andrews, Field
Supervisor, U.S. Fish and Wildlife
Service, Kentucky Ecological Services
Field Office, J.C. Watts Federal
Building, 330 W. Broadway Rm. 265,
Frankfort, KY 40601; telephone 502–
695–0468; facsimile 502–695–1024.
For information regarding the rush
darter, contact Stephen Ricks, Field
Supervisor, U.S. Fish and Wildlife
Service, Mississippi Ecological Services
Field Office, 6578 Dogwood View
Parkway, Suite A, Jackson, MS 39213;
telephone 601–965–4900; facsimile
601–965–4340 or Bill Pearson, Field
Supervisor, U.S. Fish and Wildlife
Service, Alabama Ecological Services
Field Office, 1208–B Main Street,
Daphne, AL 36526; telephone 251–441–
5181; fax 251–441–6222.
For information regarding the
yellowcheek darter, contact Jim Boggs,
Field Supervisor, U.S. Fish and Wildlife
Service, Arkansas Ecological Services
Field Office, 110 South Amity Road,
Suite 300, Conway, AR 72032;
telephone 501–513–4470; facsimile
501–513–4480.
For information regarding the chucky
madtom and laurel dace, contact Mary
Jennings, Field Supervisor, U.S. Fish
and Wildlife Service, Tennessee
Ecological Services Field Office, 446
Neal Street, Cookeville, TN 38501;
telephone 931–528–6481; facsimile
931–528–7075.
If you use a telecommunications
device for the deaf (TDD), call the
Federal Information Relay Service
(FIRS) at 800–877–8339.
SUPPLEMENTARY INFORMATION:
Background
This document consists of a final rule
to list the Cumberland darter
(Etheostoma susanae), rush darter
(Etheostoma phytophilum), yellowcheek
darter (Etheostoma moorei), chucky
madtom (Noturus crypticus), and laurel
dace (Chrosomus saylori) as endangered
under the Endangered Species Act of
1973, as amended (16 U.S.C. 1531 et
seq.) (Act). The Act requires that we
identify species of wildlife and plants
that are endangered or threatened, based
on the best available scientific and
commercial information. As defined in
section 3 of the Act, an endangered
species is any species which is in
danger of extinction throughout all or a
significant portion of its range, and a
48723
threatened species is any species which
is likely to become an endangered
species within the foreseeable future
throughout all or a significant portion of
its range.
Through the Federal rulemaking
process, we add species that meet these
definitions to the List of Endangered
and Threatened Wildlife at 50 CFR
17.11 or the List of Endangered and
Threatened Plants at 50 CFR 17.12. As
part of this program, we maintain a list
of species that we regard as candidates
for listing. We call this list the
Candidate Notice of Review (CNOR). A
candidate species is one for which we
have on file sufficient information on
biological vulnerability and threats to
support a proposal to list as endangered
or threatened, but for which preparation
and publication of a proposal is
precluded by higher priority listing
actions. We may identify a species as a
candidate for listing based on an
evaluation of its status that we
conducted on our own initiative, or as
a result of making a finding on a
petition to list a species that listing is
warranted but precluded by other higher
priority listing action. Table 1 includes
the citation information for the CNORs
mentioned in the following paragraphs,
which discuss the previous candidate
status of each of the five species being
listed as endangered in this rule.
TABLE 1—FEDERAL REGISTER CITATION INFORMATION FOR CERTAIN CANDIDATE NOTICES OF REVIEW ISSUED BY THE
U.S. FISH AND WILDLIFE SERVICE SINCE 1985
Federal Register
volume and page
number
Year
1985
1989
1991
1994
1996
1999
2001
2002
2004
2005
2006
2007
2008
2009
2010
.......................................................
.......................................................
.......................................................
.......................................................
.......................................................
.......................................................
.......................................................
.......................................................
.......................................................
.......................................................
.......................................................
.......................................................
.......................................................
.......................................................
.......................................................
50
54
56
59
61
64
66
67
69
70
71
72
73
74
75
Previous Federal Action
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Cumberland Darter
The Cumberland darter was first
identified as a candidate for listing in
the 1985 CNOR. It was assigned a
Category 2 status, which was given to
those species for which the Service
possessed information indicating that
proposing to list as endangered or
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FR
FR
FR
FR
FR
FR
FR
FR
FR
FR
FR
FR
FR
FR
FR
Date of publication
in the
Federal Register
37958 .........................................................................................................
554 .............................................................................................................
58804 .........................................................................................................
58982 .........................................................................................................
7596 ...........................................................................................................
57533 .........................................................................................................
54807 .........................................................................................................
40657 .........................................................................................................
24875 .........................................................................................................
24869 .........................................................................................................
53755 .........................................................................................................
69034 .........................................................................................................
75176 .........................................................................................................
57804 .........................................................................................................
69222 .........................................................................................................
threatened was possibly appropriate,
but for which conclusive data on
biological vulnerability and threat was
not currently available to support
proposed rules. The Cumberland darter
retained the Category 2 status in the
1989, 1991, and 1994 CNORs.
Assigning categories to candidate
species was discontinued in 1996, and
only species for which the Service had
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September 18, 1985.
January 6, 1989.
November 21, 1991.
November 15, 1994.
February 28, 1996.
October 25, 1999.
October 30, 2001.
June 13, 2002.
May 4, 2004.
May 11, 2005.
September 12, 2006.
December 6, 2007.
December 10, 2008.
November 9, 2009.
November 10, 2010.
sufficient information on biological
vulnerability and threats to support
issuance of a proposed rule were
regarded as candidate species.
Candidate species were also assigned
listing priority numbers based on
immediacy and the magnitude of threat,
as well as their taxonomic status. In the
1999, 2001, 2002, and 2004 CNORs, the
Cumberland darter was identified as a
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Federal Register / Vol. 76, No. 153 / Tuesday, August 9, 2011 / Rules and Regulations
listing priority 6 candidate species. We
published a petition finding for
Cumberland darter in the 2005 CNOR in
response to a petition received on May
11, 2004, stating the darter would retain
a listing priority of 6.
In the 2006 CNOR, we changed the
listing priority number for Cumberland
darter from 6 to 5, because it was
formally described as a distinct species.
Based on new molecular evidence, the
subspecies Etheostoma nigrum susanae
was elevated to specific status,
Etheostoma susanae. In the 2007, 2008,
2009, and 2010 CNORs, the Cumberland
darter retained a listing priority of 5. On
June 24, 2010 (75 FR 36035) we
published a proposed rule to list the
Cumberland darter as endangered.
Rush Darter
We first identified the rush darter as
a candidate for listing in the 2002
CNOR. The rush darter was assigned a
listing priority number of 5. In the 2004
CNOR, the rush darter retained a listing
priority number of 5. We published a
petition finding for rush darter in the
2005 CNOR in response to a petition
received on May 11, 2004, stating the
darter would retain a listing priority of
5.
In 2006, we changed the listing
priority number of the rush darter from
5 to 2 based on the imminent threat of
water quality deterioration (i.e.,
increased sedimentation due to
urbanization, road maintenance, and
silviculture practices). In the 2007,
2008, 2009, and 2010 CNORs, the rush
darter retained a listing priority of 2. We
proposed to list the rush darter as
endangered on June 24, 2010 (75 FR
36035).
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Yellowcheek Darter
We first identified the yellowcheek
darter as a candidate for listing in the
2001 CNOR with a listing priority of 2.
The yellowcheek darter retained a
listing priority number of 2 in the 2002
and 2004 CNORs. We published a
petition finding for yellowcheek darter
in the 2005 CNOR in response to a
petition received on May 11, 2004,
stating the darter would retain a listing
priority of 2.
In the 2006, 2007, 2008, 2009, and
2010 CNORs, the yellowcheek darter
retained a listing priority of 2. The
yellowcheek darter is covered by a 2007
programmatic Candidate Conservation
Agreement with Assurances (71 FR
53129) that covers the entire range of
the species. We proposed to list the
yellowcheek darter as endangered on
June 24, 2010 (75 FR 36035).
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Chucky Madtom
We first identified the chucky
madtom as a candidate for listing in the
1994 CNOR with a Category 2 status. In
the 2002 and 2004 CNORs, the chucky
madtom was identified as a listing
priority 2 candidate species. We
published a petition finding for chucky
madtom in the 2005 CNOR in response
to a petition received on May 11, 2004,
stating the madtom would retain a
listing priority of 2. In the 2006, 2007,
2008, 2009, and 2010 CNORs, the
chucky madtom retained a listing
priority of 2.
In 1994, the chucky madtom was first
added to the candidate list as Noturus
sp. Subsequently, and based on
morphological and molecular evidence,
the chucky madtom was formally
described as a distinct species, Noturus
crypticus (Burr et al. 2005). We
included this new information in the
2006 CNOR. We proposed to list the
chucky madtom as endangered on June
24, 2010 (75 FR 36035).
Laurel Dace
We first identified the laurel dace as
a new candidate for listing in the 2007
CNOR. New candidates are those taxa
for which we have sufficient
information on biological vulnerability
and threats to support preparation of a
listing proposal, but for which
development of a listing regulation is
precluded by other higher priority
listing activities.
In the 2007 CNOR, we assigned the
laurel dace a listing priority of 5. The
laurel dace retained a listing priority of
5 in the 2008, 2009, and 2010 CNORs.
We proposed to list the laurel dace as
endangered on June 24, 2010 (75 FR
36035).
Species Information
Cumberland Darter
The Cumberland darter (Etheostoma
(Boleosoma) susanae (Jordan and
Swain)) is a medium-sized member of
the fish tribe Etheostomatini (family
Percidae) that reaches over 5.5
centimeters (cm) (2 inches (in)) standard
length (SL) (length from tip of snout to
start of the caudal peduncle (slender
region extending from behind the anal
fin to the base of the caudal fin)) (Etnier
and Starnes 1993, p. 512). The species
has a straw-yellow background body
color with brown markings that form six
evenly spaced dorsal (back) saddles and
a series of X-, C-, or W-shaped markings
on its sides (Etnier and Starnes 1993, p.
510). During spawning season, the
overall body color of breeding males
darkens, and the side markings become
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obscure or appear as a series of blotches
(Etnier and Starnes 1993, p. 510).
The Cumberland darter was first
described as Boleosoma susanae by
Jordan and Swain (1883, pp. 249–250)
from tributaries of the Clear Fork of the
Cumberland River, Kentucky.
Subsequent studies by Kuhne (1939, p.
92) and Cole (1967, p. 29) formerly
recognized the taxon as a subspecies
(Etheostoma nigrum susanae) of E. n.
nigrum (Johnny darter). Starnes and
Starnes (1979, p. 427) clarified the
subspecific status of the Cumberland
darter, differentiating it from the Johnny
darter by several diagnostic
characteristics. Strange (1998, p. 101)
elevated E. n. susanae to full species
status based on analyses of
mitochondrial DNA for E. n. susanae
and E. n. nigrum.
The Cumberland darter inhabits pools
or shallow runs of low- to moderategradient sections of streams with stable
sand, silt, or sand-covered bedrock
substrates (O’Bara 1988, pp. 10–11;
O’Bara 1991, p. 10; Thomas 2007, p. 4).
Thomas (2007, p. 4) did not encounter
the species in high-gradient sections of
streams or areas dominated by cobble or
boulder substrates. Thomas (2007, p. 4)
reported that streams inhabited by
Cumberland darters were second to
fourth order, with widths ranging from
4 to 9 meters (m) (11 to 30 feet (ft)) and
depths ranging from 20 to 76 cm (8 to
30 in).
Little is known regarding the
reproductive habits of the Cumberland
darter. Thomas (2007, p. 4) reported the
collection of males in breeding
condition in April and May, with water
temperatures ranging from 15 to 18
degrees Celsius (°C) (59 to 64 degrees
Fahrenheit (°F)). Extensive searches by
Thomas (2007, p. 4) produced no
evidence of nests or eggs at these sites.
Species commonly associated with the
Cumberland darter during surveys by
Thomas (2007, pp. 4–5) were creek chub
(Semotilus atromaculatus), northern
hogsucker (Hypentelium nigricans),
stripetail darter (E. kennicotti), and
Cumberland arrow darter (E. sagitta
sagitta). Feeding habits are unknown
but are likely similar to that of the
closely related species, the Johnny
darter (E. nigrum). Johnny darters are
sight feeders, with prey items consisting
of midge larvae, mayfly nymphs,
caddisfly larvae, and microcrustaceans
(Etnier and Starnes 1993, p. 511).
Thomas (2007, p. 5) collected
individuals of the Federally threatened
blackside dace (Chrosomus
cumberlandensis), from three streams
that also supported Cumberland darters.
The Cumberland darter is endemic to
the upper Cumberland River system
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above Cumberland Falls in Kentucky
and Tennessee (O’Bara 1988, p. 1;
O’Bara 1991, p. 9; Etnier and Starnes
1993, p. 511). The earliest known
collections of the species were made by
Jordan and Swain (1883, pp. 249–250),
who recorded it as abundant in
tributaries of Clear Fork of the
Cumberland River, Kentucky. The
species was later reported from Gum
Fork, Scott County, Tennessee, by
Shoup and Peyton (1940, p. 11), and
seven additional tributaries of the
Cumberland River by Burr and Warren
(1986, p. 310). More exhaustive surveys
by O’Bara (1988, p. 6; 1991, pp. 9–10)
and Laudermilk and Cicerello (1998; pp.
83–233, 303–408) determined that the
Cumberland darter was restricted to
short reaches of 20 small streams (23
sites) in the upper Cumberland River
system in Whitley and McCreary
Counties, Kentucky, and Campbell and
Scott Counties, Tennessee. These
studies suggested the extirpation of the
species from Little Wolf Creek in
Whitley County, Kentucky, and Gum
Fork in Scott County, Tennessee.
Preliminary reports of disjunct
populations in the Poor Fork
Cumberland River and Martins Fork in
Letcher and Harlan Counties, Kentucky
(Starnes and Starnes 1979, p. 427;
O’Bara 1988, p. 6; O’Bara 1991, pp. 9–
10), were evaluated genetically and
determined to be the Johnny darter
(Strange 1998, p. 101).
Thomas (2007, p. 3) provided the
most recent information on status and
distribution of the species through
completion of a range-wide status
assessment in the upper Cumberland
River drainage in Kentucky. Between
June 2005 and April 2007, a total of 47
sites were sampled qualitatively in the
upper Cumberland River drainage. All
Kentucky sites with historic records
were surveyed (20 sites), as well as 27
others having potentially suitable
habitat. Surveys by Thomas (2007, p. 3)
produced a total of 51 specimens from
13 localities (12 streams). Only one of
the localities represented a new
occurrence record for the species.
In 2008, the Kentucky Department of
Fish and Wildlife Resources (KDFWR)
initiated a propagation and
reintroduction project for the
Cumberland darter in the upper
Cumberland River drainage (Thomas et
al. 2010, p. 107). Utilizing State Wildlife
Grant funds from the Service, KDFWR
worked cooperatively with Conservation
Fisheries, Inc. (CFI) of Knoxville,
Tennessee, to develop captive
propagation protocols for the species
and to produce juvenile Cumberland
darters that could be reintroduced
within the species’ historic range. Cogur
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Fork, a tributary to Indian Creek in
McCreary County, Kentucky, was
chosen by KDFWR as a suitable
reintroduction site. Cumberland darters
were released into Cogur Fork in August
2009 and September 2010. Surveys in
November 2010 resulted in recaptures of
individuals released in 2009 and 2010,
as well as captures of four individuals
without tags (possibly native
individuals) (Thomas pers. comm.
2010). Based on these results, it appears
that reintroduction efforts have been
effective, with Cumberland darters
persisting within Cogur Fork since 2009.
Furthermore, captures of untagged
individuals in 2009 and 2010 suggest
that Cogur Fork also supports a small,
native population of the species.
Currently, the Cumberland darter is
known from 15 localities in a total of 13
streams in Kentucky (McCreary and
Whitley Counties) and Tennessee
(Campbell and Scott Counties). All 15
extant occurrences of the Cumberland
darter are restricted to short stream
reaches, with the majority believed to be
restricted to less than 1.6 kilometers
(km) (1 mile (mi)) of stream (O’Bara
1991, pp. 9–10; Thomas 2007, p. 3).
These occurrences are thought to form
six population clusters (Bunches Creek,
Indian Creek, Marsh Creek, Jellico
Creek, Clear Fork, and Youngs Creek),
which are geographically separated from
one another by an average distance of
30.5 stream km (19 stream mi) (O’Bara
1988, p. 12; O’Bara 1991, p. 10; Thomas
2007, p. 3). Based on collection efforts
by O’Bara (1991, pp. 9–10), Laudermilk
and Cicerello (1998; pp. 83–233, 303–
408), and Thomas (2007, p. 3), the
species appears to be extirpated from 11
historical collection sites and a total of
9 streams: Cumberland River mainstem,
near the mouth of Bunches Creek and
Cumberland Falls (Whitley County);
Sanders Creek (Whitley County); Brier
Creek (Whitley County); Kilburn Fork of
Indian Creek (McCreary County); Bridge
Fork (McCreary County); Marsh Creek,
near mouth of Big Branch and Caddell
Branch (McCreary County); Cal Creek
(McCreary County); Little Wolf Creek
(Whitley County); and Gum Fork (Scott
County). No population estimates or
status trends are available for the
Cumberland darter; however, survey
results by Thomas (2007, p. 3) suggest
that the species is uncommon or occurs
in low densities across its range
(Thomas 2007, p. 3).
The Cumberland darter is ranked by
the Kentucky State Nature Preserves
Commission (KSNPC) (2009, p. 38) and
the Tennessee Department of
Environment and Conservation (TDEC)
(2009, p. 53) as a G1G2S1 species:
critically imperiled or imperiled
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48725
globally and critically imperiled in
Kentucky and Tennessee. The KDFWR
State Wildlife Action Plan identified the
Cumberland darter as a species of
Greatest Conservation Need (GCN) and
identified several top conservation
actions for it and other species in its
Aquatic Guild (Upland Headwater
Streams in Pools), including:
Acquisition or conservation easements
for critical habitat, development of
financial incentives to protect riparian
(land adjacent to stream channel)
corridors, development and
implementation of best management
practices, and restoration of degraded
habitats through various State and
Federal programs (KDFWR 2005, p.
2.2.2). The Cumberland darter is
designated as a Tier 1 GCN species in
the Tennessee Comprehensive Wildlife
Conservation Strategy (CWCS) (TWRA
2005, pp. 44, 49).
Rush Darter
The rush darter (Etheostoma
phytophilum) is a medium-sized darter
in the family Percidae, tribe
Etheostomatini, and subgenus
Fuscatelum. The species reaches an
average size of 5 cm (2 in) SL (Bart and
Taylor 1999, p. 28; Johnston and Kleiner
2001, p. 3). The rush darter was
described by Bart and Taylor in 1999
(pp. 27–33), and is closely related to the
goldstripe darter (E. parvipinne), a drabcolored species with a thin golden stripe
along the lateral line (canal along the
side of a fish with sensory capabilities)
that is surrounded by heavily mottled or
stippled sides (Shaw 1996, p. 85).
However, the distinct golden stripe
characteristic of goldstripe darters is not
well developed in rush darters (Bart and
Taylor 1999, p. 29). Also, the brown
pigment on the sides of the rush darter
is usually not as intense as in the
goldstripe darter. Other characteristics
of the rush darter are described in Bart
and Taylor (1999, p. 28).
Rush darters have been collected from
various habitats (Stiles and Mills 2008,
pp. 1–4; Bart 2002, p. 1; Johnston and
Kleiner 2001, pp. 3–4; Stiles and
Blanchard 2001, pp. 1–4; Bart and
Taylor 1999, p. 32), including root
masses of emergent vegetation along the
margins of spring-fed streams in very
shallow, clear, cool, and flowing water;
and from both small clumps and dense
stands of bur reed (Sparganium sp.),
coontail (Ceratophyllum sp.), watercress
(Nasturtium officinale), and rush
(Juncus sp.) in streams with substrates
of silt, sand, sand and silt, muck and
sand or some gravel with sand, and
bedrock. Rush darters appear to prefer
springs and spring-fed reaches of
relatively low-gradient small streams,
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which are generally influenced by
springs (Stiles and Mills 2008, pp. 1–4;
Fluker et al. 2007, p. 1; Bart 2002, p. 1;
Johnston and Kleiner 2001, pp. 3–4;
Stiles and Blanchard 2001, pp. 1–4; Bart
and Taylor 1999, p. 32). Rush darters
have also been collected in wetland
pools (Stiles and Mills 2008; pp. 2–3).
Water depth at collection sites ranged
from 3.0 cm to 0.5 m (0.1 ft to 1.6 ft),
with moderate water velocity in riffles
and no flow or low flow in pools. Rush
darters have not been found in higher
gradient streams with bedrock
substrates and sparse vegetation (Stiles
and Mills 2008, pp. 1–4; Bart 2002, p.
1; Johnston and Kleiner 2001, pp. 3–4;
Stiles and Blanchard 2001, pp. 1–4; Bart
and Taylor 1999, p. 32).
Stiles and Mills (2008, p. 2) found
gravid rush darter females in February
and fry (newly hatched larval fish) in
late April from a wetland pool in the
Mill Creek watershed (Winston County,
Alabama). These pools act as nursery
areas for the fry (Stiles and Mills 2008,
p. 5). While little is known specifically
about the life history of the rush darter,
this information is available for the
goldstripe darter, a related species in the
Etheostoma genus. Spawning of the
goldstripe darter in Alabama occurs
from mid-March through June (Mettee et
al. 1996, p. 655). Preferred food items
for the goldstripe darter include midge
larvae, mayfly nymphs, blackfly larvae,
beetles, and microcrustaceans (Mettee et
al. 1996, p. 655). The lifespan of the
goldstripe darter is estimated to be 2 to
3 years.
The rush darter currently has a
restricted distribution (Johnston and
Kleiner 2001, p. 1). All rush darter
populations are located above the Fall
Line (the inland boundary of the Coastal
Plain physiographic region) and in other
‘‘highland regions’’ where topography
and elevation changes are observed
presenting a barrier for fish movement
(Boshung and Mayden 2004, p. 18) in
the Black Warrior River drainage in
portions of the Appalachian Plateau and
Valley and Ridge physiographic
provinces of Alabama (Boshung and
Mayden 2004, pp. 16–17; Warren et al.
2000, pp. 9, 10, 24). The closely related
goldstripe darter in Alabama occurs
essentially below the Fall Line in all
major systems except the Coosa system
(Boshung and Mayden 2004, p. 550).
Reports of goldstripe darters from the
1960s and 1970s in Winston and
Jefferson Counties, Alabama (Caldwell
1965, pp. 13–14; Barclay 1971, p. 38;
Dycus and Howell 1974, pp. 21–24;
Mettee et al. 1989, pp. 13, 61, 64), which
are above the Fall Line, were made prior
to the description of the rush darter, but
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are now considered to be rush darters
(Kuhajda pers. comm. 2008).
Historically, rush darters have been
found in three distinct watersheds in
Alabama: Doe Branch, Wildcat Branch,
and Mill Creek of the Clear Creek
drainage in Winston County; an
unnamed spring run of Beaver Creek
and Penny Springs of the Turkey Creek
drainage in Jefferson County; and Cove
Spring (Little Cove Creek system) and
Bristow Creek of the Locust Fork
drainage in Etowah County. Fluker et al.
(2007, p. 10) suggests that the unique
topographic and geologic influences in
the three distinct population groups
likely produced different selective
pressures, genetic isolation, genetic
drift, and divergence during the species’
evolution.
Currently, the three rush darter
populations occur in the same
watersheds but in a more limited
distribution. One population is located
in Wildcat Branch and Mill Creek in the
Clear Creek drainage in Winston County
(Johnston and Kleiner 2001, p. 4; Stiles
and Mills 2008, pp. 1–3); the second is
located in an unnamed spring run to
Beaver Creek, portions of Beaver Creek,
and an unnamed tributary to Turkey
Creek in the Turkey Creek drainage in
Jefferson County (Stiles and Blanchard
2001, p. 2; Drennen pers. obsv. 2006–
2010; Kuhajda pers. comm. 2009); and
the third is in the Little Cove Creek
drainage (Bart and Taylor 1999, p. 28;
Bart 2002, p. 7; Kuhajda pers. comm.
2008–2009; Spadgenski pers. comm.
2008–2009).
Rush darter populations are separated
from each other geographically, and
individual rush darters are only
sporadically collected at a particular site
within their range. Where it occurs, the
rush darter is apparently an uncommon
species that is usually collected in low
numbers (compiled from Bart and
Taylor 1999, pp. 31–32; Johnston and
Kleiner 2001, pp. 2–4; Stiles and
Blanchard 2001, pp. 1–4; Johnston 2003,
pp. 1–3; Stiles and Mills 2008, pp. 1–
3; Rakes pers. comm. 2010; Drennen
pers. obsv. 2006–2010; Kuhajda pers.
comm. 2009); however, there are no
population estimates at this time.
Cumulatively, the rush darter is only
known from localized collection sites
within approximately 14.5 km (9 mi) of
streams in the Clear Creek; Little Cove
and Bristow Creek; and Turkey Creek
drainages in Winston, Etowah, and
Jefferson Counties, respectively.
Currently, about 3 km (2 mi) of stream,
or about 22 percent of the rush darter’s
known range, is not occupied.
Within the Clear Creek drainage, the
rush darter has been collected in
Wildcat Branch, Mill Creek, and Doe
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Creek, which represents about 13 km (9
mi) of stream or about 89 percent of the
species’ total cumulative range. Recent
surveys (Stiles and Mills 2008, pp. 1–4;
Johnston and Kleiner 2001, p. 3) have
failed to document the absence of the
rush darter in Doe Creek, indicating a
potential reduction of the species’
known range within the Clear Creek
drainage by about 3 km (2 mi) of stream
or 22 percent. However, rush darters
were collected in 2005, 2008, and 2009
in the Little Cove Creek drainage (Cove
Spring run), after a 30 year period of not
finding the species. This rediscovery of
the species confirms the continued
existence of the species in Etowah
County and Cove Spring. However, the
Little Cove Creek drainage constitutes
an increase of only 0.05 km (0.02 mi) of
occupied stream habitat or a 0.22
percent addition to the total range of the
species. No collections of the species
have occurred at Bristow Creek since
1997. Bristow Creek has since been
channelized (straightened and deepened
to increase water velocity). In the
Turkey Creek drainage, rush darters
have been collected sporadically within
Penny Springs and at the type locality
for the species (an unnamed spring run
in Jefferson County, Alabama) (Bart and
Taylor 1999, pp. 28, 33). However, the
rush darter is likely extirpated from
Penny and Tapawingo Springs due to
introductions of the watercress darter
(E. nuchale) (George et al. 2009, p. 532).
The species can still be found in
portions of an unnamed tributary of
Beaver Creek and an unnamed spring to
Beaver Creek (Kuhajda pers. comm.
2009). This area contains about 1.6 km
(1 mi) of occupied stream habitat or
approximately 11 percent of the rush
darter’s total range.
The rush darter is ranked by the
Alabama Department of Conservation
and Natural Resources (ADCNR)
(Wildlife and Freshwater Fisheries
Division, ADCNR 2005) as a P1G1S1
species signifying its rarity in Alabama
and its status as critically imperiled
globally. It is also considered a species
of GCN by the State (Bart 2004, p. 193).
The rush darter has a High Priority
Conservation Actions Needed and Key
Partnership Opportunities ranking of
‘‘CA 6,’’ the highest of any fish species
listed. The State Wildlife Action Plan
states that the species consists of
disjoint populations and information is
needed to determine genetic structuring
within the populations (Wildlife and
Freshwater Fisheries Division, ADCNR
2005). Conservation Actions for the
species may require population
augmentation or reintroduction of the
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species to suitable habitats to maintain
viability.
Yellowcheek Darter
The yellowcheek darter (Etheostoma
moorei) is a small and laterallycompressed fish that attains a maximum
SL of about 6.4 cm (2.5 in), and has a
moderately sharp snout, deep body, and
deep caudal peduncle (Raney and
Suttkus 1964, p. 130). The back and
sides are grayish brown, often with
darker brown saddles and lateral bars.
Breeding males are brightly colored
with a bright blue or brilliant turquoise
throat and breast and a light-green belly,
while breeding females possess orange
and red-orange spots but are not brightly
colored (Robison and Buchanan 1988,
pp. 427–429).
First collected in 1959 from the Devils
Fork Little Red River, Cleburne County,
Arkansas, this species was eventually
described by Raney and Suttkus in
1964, using 228 specimens from the
Middle, South, and Devils Forks of the
Little Red River (Devils Fork, Turkey
Fork, and Beech Fork represent one
stream with three different names and
are subsequently referred to in this rule
as ‘‘Devils Fork’’). Wood (1996, p. 305)
verified the taxonomic status of the
yellowcheek darter within the subgenus
Nothonotus. Complete taxonomy for the
species is family Percidae, subfamily
Percinae, tribe Etheostomatini, genus
Etheostoma, subgenus Nothonotus and
E. tippecanoe species group (Wood
1996, p. 307). The yellowcheek darter is
one of only two members of the
subgenus Nothonotus known to occur
west of the Mississippi River.
The yellowcheek darter inhabits highgradient headwater tributaries with
clear water; permanent flow; moderate
to strong riffles; and gravel, rubble, and
boulder substrates (Robison and
Buchanan 1988, p. 429). Yellowcheek
darter prey items include aquatic fly
larvae, stonefly larvae, mayfly nymphs,
and caddisfly larvae (McDaniel 1984, p.
56).
Male and female yellowcheek darters
reach sexual maturity at 1 year of age,
and maximum lifespan is around 5
years (McDaniel 1984, pp. 25, 76).
Spawning occurs from late May through
June in the swift to moderately swift
portions of riffles, often around or under
the largest substrate particles (McDaniel
1984, p. 82), although brooding females
have been found at the head of riffles in
smaller gravel substrate (Wine et al.
2000, p. 3). During nonspawning
months, there is a general movement to
portions of the riffle with smaller
substrate, such as gravel or cobble, and
less turbulence (Robison and Harp 1981,
p. 3). Weston and Johnson (2005, p. 24)
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observed that the yellowcheek darter
moved very little during a 1-year
migration study. It was noted that the
yellowcheek darter appears to be a
relatively nonmobile species, with 19 of
22 recaptured darters found within 9 m
(29.5 ft) of their original capture
position after periods of several months.
A number of life-history characteristics
including courtship patterns, specific
spawning behaviors, egg deposition
sites, number of eggs per nest, degree of
nest protection by males, and degree of
territoriality are unknown at this time;
however, researchers have suggested
that the yellowcheek darter deposits
eggs on the undersides of large rubble in
swift water (McDaniel 1984, p. 82).
Wine and Blumenshine (2002, p. 10)
noted that, during laboratory spawning,
female yellowcheek darters bury
themselves in fine gravel or sand
substrates (often behind large cobble or
boulders) with only their heads and
caudal fin exposed. A male yellowcheek
darter will then position upstream of the
buried female and fertilize her eggs as
she releases them in a vibrating motion.
Clutch size and nest defense behavior
were not observed.
The yellowcheek darter is endemic to
the Devils, Middle, South, and Archey
Forks of the Little Red River and
mainstem Little Red River in Cleburne,
Searcy, Stone, and Van Buren Counties,
Arkansas (Robison and Buchanan 1988,
p. 429). In 1962, the construction of a
dam on the Little Red River to create
Greers Ferry Reservoir impounded
much of the range of this species,
including the lower reaches of Devils
Fork, Middle Fork, South Fork, and
portions of the mainstem Little Red
River, thus extirpating the species from
these reaches. Yellowcheek darter was
also extirpated from the Little Red River
downstream of Greers Ferry Reservoir
due to cold tailwater releases. The lake
flooded optimal habitat for the species,
and caused the genetic isolation of
populations (McDaniel 1984, p. 1). The
yellowcheek darter was known to
historically occur in portions of these
streams that maintained permanent
year-round flows.
In the 1978–1981 study by Robison
and Harp (1981, pp. 15–16),
yellowcheek darter occurred in greatest
numbers in the Middle and South Forks
of the Little Red River, with populations
estimated at 36,000 and 13,500
individuals, respectively, while
populations in both Devils Fork and
Archey Fork were estimated at
approximately 10,000 individuals
(Robison and Harp 1981, pp. 5–11).
During this study, the four forks of the
Little Red River supported an estimated
yellowcheek darter population of 60,000
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individuals, and the species was
considered the most abundant riffle fish
present (Robison and Harp 1981, p. 14).
Extensive sampling of the first two
tributaries of the Little Red River below
Greers Ferry Dam (both named Big
Creek) failed to find any yellowcheek
darters, and no darters were found in
immediately adjacent watersheds
(Robison and Harp 1981, p. 5).
Two subsequent studies have failed to
observe yellowcheek darters in the
Turkey Fork reach of the Devils Fork
Little Red River (Wine et al. 2000, p. 9;
Wine and Blumenshine 2002, p. 11),
since four individuals were last
collected by Arkansas State University
(ASU) researchers in 1999 (Mitchell et
al. 2002, p. 129). They have been
observed downstream within that
system in the Beech Fork reach, where
flows are more permanent. The reach
downstream of Raccoon Creek is
influenced by inundation from Greers
Ferry Reservoir and no longer supports
yellowcheek darter. The U.S. Army
Corps of Engineers channelized
approximately 5.6 km (3.5 mi) of the
lower Archey and South Forks Little
Red River within the city limits of
Clinton, Arkansas, in 1985 for flood
control purposes. Yellowcheek darter
has not been collected within this reach
since channelization. The yellowcheek
darter inhabits most of its historical
range not currently affected by Greers
Ferry Lake, although in greatly reduced
numbers in the Middle, South, Archey,
and Devils Forks of the Little Red River.
While collecting specimens for the
1999 genetic study, ASU researchers
discovered that the yellowcheek darter
was no longer the most abundant riffle
fish and was more difficult to find
throughout its historical range (Wine et
al. 2000, p. 2). Because optimal habitat
had been destroyed by the creation of
Greers Ferry Lake, yellowcheek darters
were confined to upper stream reaches
with lower summer flow, smaller
substrate particle size, and reduced
gradient. A thorough status survey
conducted in 2000 found the
yellowcheek darter in three of four
historically occupied forks in greatly
reduced numbers (Wine et al. 2000, p.
9). Populations in the Middle Fork were
estimated at approximately 6,000
individuals, the South Fork at 2,300,
and the Archey Fork at 2,000.
Yellowcheek darter was not collected
from the Devils Fork. Fish community
composition was similar from 1978–
1981 and 2000 studies, but the
proportion of yellowcheek darter
declined from approximately 28 percent
to 6 percent of the overall composition.
Fish known to coexist with yellowcheek
darter include the rainbow darter (E.
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caeruleum) and greenside darter (E.
blennioides), which can use pool
habitats during periods of low flow, as
evidenced by the collection of these two
species from pools during
electroshocking activities.
Electroshocking has not revealed
yellowcheek darter in pools, suggesting
perhaps that they are unable to tolerate
pool conditions (deep, slow-moving
water usually devoid of cobble
substrate). An inability to use pools
during low flows would make them
much more vulnerable to seasonal
fluctuations in flows that reduce riffle
habitat. As a result, researchers have
suggested that yellowcheek darter
declines are more likely a species rather
than community phenomenon (Wine et
al. 2000, p. 11).
Weston and Johnson (2005, p. 22)
estimated yellowcheek darter
populations within the Middle Fork to
be between 15,000 and 40,000
individuals, and between 13,000 and
17,000 individuals in the South Fork.
Such increases since the 2000 status
survey would indicate remarkable
adaptability to changing environmental
conditions. However, it should be noted
that estimates were based upon mark/
recapture estimates using the Jolly-Seber
method, which requires high numbers
of recaptured specimens for accurate
estimations. Recaptures were extremely
low during that study; therefore,
population estimates were highly
variable and confidence in the resulting
estimates is low.
The yellowcheek darter is ranked by
the Arkansas Natural Heritage
Commission (ANHC) (2007, pp. 2–118)
as an S1G1 species: extremely rare in
Arkansas, and critically imperiled
globally. The Arkansas Game and Fish
Commission’s (AGFC) Wildlife Action
Plan describes the yellowcheek darter as
a critically imperiled species with
declining populations (AGFC 2005, pp.
452–454).
Chucky Madtom
The chucky madtom (Noturus
crypticus) is a small catfish (family
Ictaluridae), with the largest specimen
measuring 6.5 cm (2.6 in) SL (Burr et al.
2005, p. 795). Burr et al. (2005)
described the chucky madtom,
confirming previous analyses (Burr and
Eisenhour 1994), which indicated that
the chucky madtom is a unique species,
a member of the Rabida subgenus (i.e.,
the ‘‘mottled’’ or ‘‘saddled’’ madtoms),
and a member of the Noturus elegans
species complex (i.e., N. elegans, N.
albater, N. fasciatus, and N. trautmani)
outlined by Taylor (1969 in Grady and
LeGrande 1992). A robust madtom, the
chucky madtom body is wide at the
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pectoral fin origins, greater than 23
percent of the SL. The back contains
three dark, nearly black blotches ending
abruptly above the lateral midline of the
body, with a moderately contrasting,
oval, pale saddle in front of each blotch
(Burr et al. 2005, p. 795).
The chucky madtom is a rare catfish
known from only 15 specimens
collected from two Tennessee streams.
A lone individual was collected in 1940
from Dunn Creek (a Little Pigeon River
tributary) in Sevier County, and 14
specimens have been encountered since
1991 in Little Chucky Creek (a
Nolichucky River tributary) in Greene
County, Tennessee. Only 3 chucky
madtom individuals have been
encountered since 2000; 1 in 2000 (Lang
et al. 2001, p. 2) and 2 in 2004 (CFI
2008, unpublished data), despite
surveys that have been conducted in
both historical localities at least twice a
year since 2000 (Rakes and Shute 2004,
pp. 2–3; Weber and Layzer 2007, p. 4;
CFI 2008, unpublished data). In
addition, several streams in the
Nolichucky, Holston, and French Broad
River watersheds of the upper
Tennessee River basin, which are
similar in size and character to Little
Chucky Creek, have been surveyed with
no success (Burr and Eisenhour 1994,
pp. 1–2; Shute et al. 1997, p. 5; Lang et
al. 2001, pp. 2–3; Rakes and Shute 2004,
p. 1). Conservation Fisheries, Inc. did
not find chucky madtoms in 2007 after
attempting new sampling techniques
(e.g., PVC ‘‘jug’’ traps) (CFI 2008,
unpublished data).
Originally, museum specimens
collected from the Roaring River in
Tennessee (Cumberland River drainage)
and from Piney Creek, West Fork Flint
River, and the Paint Rock River system
in Alabama (Tennessee River drainage)
were first identified and catalogued as
Noturus elegans species complex and
thought to be chucky madtoms. The
Roaring River, Piney Creek, and West
Fork Flint River specimens are now
considered to be a member of the N.
elegans group, but have not been
assigned to a species. While the
specimens from the Paint Rock River
system share typical anal ray counts
with the chucky madtom, they lack the
distinctive cheek characteristics, differ
in pelvic ray counts, and are
intermediately shaped between the
chucky and saddled madtoms (N.
fasciatus) with respect to body width as
a proportion of SL (Burr et al. 2005, p.
796). Thus, the Little Chucky and Dunn
Creek forms are the only forms that are
recognized as chucky madtoms.
All of the specimens collected in
Little Chucky Creek have been found in
stream runs with slow to moderate
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current over pea gravel, cobble, or slabrock substrates (Burr and Eisenhour
1994, p. 2). Habitat of these types is
sparse in Little Chucky Creek, and the
stream affords little loose, rocky cover
suitable for madtoms (Shute et al. 1997,
p. 8). It is notable that intact riparian
buffers are present in the locations
where chucky madtoms have been
found (Shute et al. 1997, p. 9).
No studies to determine the life
history and behavior of this species
have been conducted. While nothing is
known specifically about chucky
madtom reproductive biology,
recruitment, growth and longevity, food
habits, or mobility, this information is
available for other similar members of
the Noturus group. The least madtom
(N. hildebrandi) may reach sexual
maturity at 1 or more years of age (i.e.,
during their second summer) (Mayden
and Walsh 1984, p. 351). Only the
largest females of Ozark madtom (N.
albater) were found to be sexually
mature, and males were found to be
sexually mature primarily within the
second age class (Mayden et al. 1980, p.
339), though, a single large male of the
first age class showed evidence of
sexual maturity (Mayden et al. 1980, p.
339). The breeding season of the least
and smoky madtoms (N. baileyi) is
primarily during June through July,
though development of breeding
condition is initiated as early as April
in least madtom and May in smoky
madtom (Mayden and Walsh 1984, p.
353; Dinkins and Shute 1996, p. 56).
Fecundity varied among the species for
which data were available; however, it
should be noted that fecundity in
madtoms is generally lower in
comparison to other North American
freshwater fishes (Breder and Rosen
1966 in Dinkins and Shute 1996, p. 58).
Dinkins and Shute (1996, p. 58)
commented that for smoky madtom the
combination of relatively large egg size
and high level of parental care given to
the fertilized eggs and larvae reduce
early mortality and, therefore, the need
to produce a large number of young.
Both smoky and elegant madtoms (N.
elegans) were found to nest under flat
rocks at or near the head of riffles
(Dinkins and Shute 1996, p. 56; Burr
and Dimmick 1981, p. 116). Shallow
pools were also used by the smoky
madtom, which was observed to select
rocks of larger dimension for nesting
than were used for shelter during other
times of year (Dinkins and Shute 1996,
p. 56). Single madtoms were found to
guard nests in smoky and elegant
madtoms, a behavior also exhibited by
Ozark and least madtoms (Dinkins and
Shute 1996, p. 56; Burr and Dimmick
1981, p. 116; Mayden et al. 1980, p. 337;
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Mayden and Walsh 1984, p. 357). Males
of these species were the nest guardians
and many were found to have empty
stomachs suggesting that they do not
feed during nest guarding, which can
last as long as 3 weeks.
Conservation Fisheries, Inc. had one
male chucky madtom in captivity from
2004 through 2008. However, based on
information from other members of this
genus for which longevity data are
available, least and smoky madtoms, it
is unlikely that chucky madtoms can
survive this long in the wild. The
shorter lived of these, least madtom,
reached a maximum age of 18 months,
though most individuals lived little
more than 12 months, dying soon after
reproducing (Mayden and Walsh 1984,
p. 351). Based on length-frequency
distributions, smoky madtoms exhibited
a lifespan of 2 years, with two cohorts
present in a given year (Dinkins and
Shute 1996, p. 53). Collection of two age
classes together provided evidence that
life expectancy exceeds 1 year in the
pygmy madtom (N. stanauli) (Etnier and
Jenkins 1980, p. 20). The Ozark madtom
lives as long as 3 years (Mayden et al.
1980, p. 337).
Chucky madtom prey items are
unknown; however, least madtom prey
items include midge larvae, caddisfly
larvae, stonefly larvae, and mayfly
nymphs (Mayden and Walsh 1984, p.
339). In smoky madtoms, mayfly
nymphs comprised 70.7 percent of
stomach contents analyzed; fly,
mosquitoe, midge, and gnat larvae 2.4
percent; caddisfly larvae 4.4 percent;
and stonefly larvae 1.0 percent (Dinkins
and Shute 1996, p. 61). Significant
daytime feeding was observed in smoky
madtoms.
Dinkins and Shute (1996, p. 50) found
smoky madtoms underneath slabrocks
in swift to moderate current during May
to early November. Habitat use shifted
to shallow pools over the course of a 1week period, coinciding with a drop in
water temperature to 7 or 8 °C (45 to 46
°F), and persisted from early November
to May. Eisenhour et al. (1996, p. 43)
collected saddled madtoms in gravel,
cobble, and slab-rock substrates in riffle
habitats with depths ranging from 0.1 to
0.3 m (0.3 to 1.0 ft). Based on their
limited number of observations,
Eisenhour et al. (1996, p. 43)
hypothesized that saddled madtoms
occupy riffles and runs in the daylight
hours and then move to pools at night
and during crepuscular hours (dawn
and dusk) to feed.
The current range of the chucky
madtom is believed to be restricted to an
approximately 3-km (1.8-mi) reach of
Little Chucky Creek in Greene County,
Tennessee. Because this species was
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also collected from Dunn Creek, a
stream that is in a different watershed
and physiographic province than Little
Chucky Creek, it is likely that the
historic range of the chucky madtom
encompassed a wider area in the Ridge
and Valley and the Blue Ridge
physiographic provinces in Tennessee
than is demonstrated by its current
distribution. A survey for the chucky
madtom in Dunn Creek in 1996 was not
successful at locating the species (Shute
et al. 1997, p. 8). The Dunn Creek
population may be extirpated (Shute et
al. 1997, p. 6; Burr et al. 2005, p. 797),
because adequate habitat and a diverse
fish community were present at the time
of the surveys, but no chucky madtoms
were found. There are no population
size estimates or status trends for the
chucky madtom due to low numbers
and only sporadic collections of
specimens.
The chucky madtom is ranked by the
TDEC (2009, p. 58) as an S1G1 species:
extremely rare in Tennessee, and
critically imperiled globally. The
chucky madtom is designated as a Tier
1 GCN species in the Tennessee CWCS
(TWRA 2005, pp. 44, 49).
Laurel Dace
The laurel dace (Chrosomus saylori),
family Cyprinidae and subfamily
Leuciscinae, has two continuous black
lateral stripes and black pigment
covering the breast and underside of the
head of nuptial (breeding) males
(Skelton 2001, p. 120). The maximum
SL observed is 5.1 cm (2 in) (Skelton
2001, p. 124). While the belly, breast,
and lower half of the head are typically
a whitish-silvery color, at any time of
the year laurel dace may develop red
coloration below the lateral stripe that
extends from the base of the pectoral
fins to the base of the caudal fin
(Skelton 2001, p. 121).
Nuptial males often acquire brilliant
coloration during the breeding season,
as the two lateral stripes, breast, and
underside of head turn intensely black
and the entire ventral (lower/
abdominal) portion of the body,
contiguous with the lower black stripe
and black breast, becomes an intense
scarlet color. All of the fins acquire a
yellow color, which is most intense in
the paired fins and less intense in the
dorsal, anal, and caudal fins. Females
also develop most of these colors,
though of lesser intensity (Skelton 2001,
p. 121). Broadly rounded pectoral fins of
males are easily discerned from the
broadly pointed fins of females at any
time during the year.
Laurel dace have been most often
collected from pools or slow runs from
undercut banks or beneath slab
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boulders, typically in first or second
order, clear, cool (maximum
temperature 26 °C or 78.8 °F) streams.
Substrates in streams where laurel dace
are found typically consist of a mixture
of cobble, rubble, and boulders, and the
streams tend to have a dense riparian
zone consisting largely of mountain
laurel (Skelton 2001, pp. 125–126).
Skelton (2001, p. 126) reported having
collected nuptial individuals from late
March until mid-June, though Call (pers.
obs. 2004) observed males in waning
nuptial color during surveys on July 22,
2004. Laurel dace may be a spawning
nest associate where syntopic (sharing
the same habitat) with nest-building
minnow species, as has been
documented in blackside dace (Starnes
and Starnes 1981, p. 366). Soddy Creek
is the only location in which Skelton
(2001, p. 126) has collected a nestbuilding minnow with laurel dace.
Skelton (2001, p. 126) reports finding as
many as three year classes in some
collections of laurel dace, though
young-of-year fish are uncommon in
collections. Observations of three year
classes indicate that laurel dace live as
long as 3 years.
Laurel dace preferred prey items
include fly larvae, stonefly larvae, and
caddisfly larvae (Skelton 2001, p. 126).
Skelton observed that the morphological
feeding traits of laurel dace, including
large mouth, short digestive tract,
reduced number of pharyngeal (located
within the throat) teeth, and primitively
shaped basioccipital bone (bone that
articulates the vertebra), all of which are
consistent with a diet consisting largely
of animal material.
Laurel dace are known historically
from seven streams on the Walden
Ridge portion of the Cumberland
Plateau, where drainages generally
meander eastward before dropping
abruptly down the plateau escarpment
and draining into the Tennessee River.
Specifically, these seven streams occur
in three independent systems: Soddy
Creek; three streams that are part of the
Sale Creek system (the Horn and Laurel
branch tributaries to Rock Creek, and
the Cupp Creek tributary to Roaring
Creek); and three streams that are part
of the Piney River system (Young’s,
Moccasin, and Bumbee creeks). Strange
and Skelton (2005, p. 8) assessed the
genetic structure within populations of
laurel dace and, based on distribution of
genetic diversity among populations,
they recognized two genetically distinct
management units; (1) The southern
populations in Sale and Soddy Creeks,
and (2) the northern population in the
Piney River system.
Skelton (2001, p. 126) considered
collections by the Tennessee Valley
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Authority (TVA) during a rotenone
survey of Laurel Branch in 1976 to
represent laurel dace that were
misidentified as southern redbelly dace
(Chrosomus erythrogaster), as was found
to be true for specimens collected by
TVA from Horn Branch in 1976, but no
specimens are available for
confirmation. In 1991, and in four other
surveys (two in 1995, one in 1996, and
one in 2004), laurel dace were not
collected in Laurel Branch, leading
Skelton to the conclusion that laurel
dace have been extirpated from this
stream (Skelton 1997, p. 13; Skelton
2001, p. 126; Skelton pers. comm. 2009).
Skelton (pers. comm. 2009) also noted
that the site was impacted by silt.
The current distribution of laurel dace
comprises six of the seven streams that
were historically occupied; the species
is considered extirpated from Laurel
Branch (see above). In these six streams,
they are known to occupy reaches of
approximately 0.3 to 8 km (0.2 to 5 mi)
in length. The laurel dace is known
from a single reach in Soddy Creek, and
surveys in 2004 produced only a single,
juvenile laurel dace (Strange and
Skelton 2005, pp. 5–6 and Appendices
1 and 2). In Horn Branch, laurel dace are
known from approximately 900 m
(2,953 ft), but have become increasingly
difficult to collect (Skelton 1997, pp.
13–14). Skelton (1997, p. 14) reports
that minnow traps have been the most
successful method for collecting live
laurel dace from Horn Branch, as it is
difficult to electroshock the fish due to
in-stream rock formations and fallen
trees. Only a single juvenile was caught
in 2004 (Strange and Skelton 2005, p. 6).
A total of 19 laurel dace were collected
from Cupp Creek during 1995 and 1996
using an electroshocker (Skelton 1996,
p. 14). However, Skelton found no
laurel dace in this stream in 2004,
despite attempts to collect throughout
an approximately 700-m (2,297-ft) reach
(Strange and Skelton 2005, p. 6).
Laurel dace were initially found in
Young’s, Moccasin, and Bumbee creeks
in the Piney River system in 1996
(Skelton 1997, pp. 14–15). Sampling in
2004 led to the discovery of additional
laurel dace localities in Young’s and
Moccasin creeks, but the locality where
laurel dace were found in Young’s Creek
in 1996 was inaccessible due to the
presence of a locked gate (Strange and
Skelton 2005, p. 6–7). The new
localities were in the headwaters of
these two streams. Persistence of laurel
dace at the Bumbee Creek locality was
confirmed in 2004 by surveying from a
nearby road using binoculars. Direct
surveys were not possible because the
land had been leased to a hunt club for
which contact information was not
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available, and, therefore, survey
permission could not be obtained
(Strange and Skelton 2005, p. 7).
Nuptial males are easily identified from
other species present in Bumbee Creek
due to their brilliant coloration during
the breeding season, as the two lateral
stripes, breast, and underside of head
turn intensely black and the entire
ventral (lower/abdominal) portion of the
body, contiguous with the lower black
stripe and black breast, becomes an
intense scarlet color. This brilliant
coloration is easily seen through
binoculars at short distances by trained
individuals.
No population estimates are available
for laurel dace. However, based on
trends observed in surveys and
collections since 1991, Strange and
Skelton (2005, p. 8) concluded that this
species is persisting in Young’s,
Moccasin, and Bumbee creeks in the
Piney River watershed, but is at risk of
extirpation from the southern part of
Walden Ridge in Soddy Creek, and in
the Horn Branch and Cupp Creek areas
that are tributaries to Sale Creek. As
noted above, the species is considered
to be extirpated from Laurel Branch,
which is part of the Sale Creek system.
The laurel dace is ranked by the TDEC
(2009, p. 60) as an S1G1 species:
extremely rare in Tennessee, and
critically imperiled globally. The laurel
dace is designated as a Tier 1 GCN
species in the Tennessee CWCS (TWRA
2005, pp. 44, 49).
Summary of Comments and
Recommendations
In the proposed rule published on
June 24, 2010, we requested that all
interested parties submit written
comments on the proposed rule to list
the Cumberland darter, rush darter,
yellowcheek darter, chucky madtom,
and laurel dace by August 23, 2010. We
also contacted appropriate Federal and
State agencies, scientific experts and
organizations, and other interested
parties and invited them to comment on
the proposal. Newspaper notices
inviting general public comment were
published in newspapers covering all
affected counties in Kentucky,
Tennessee, Alabama, and Arkansas. We
did not receive any requests for a public
hearing.
During the comment period for the
proposed rule, we received ten
comment letters in response to the
proposed rule: four from peer reviewers,
one from a State agency, and five from
organizations or individuals. All of the
ten commenters supported the proposed
rule to list these five fishes as
endangered. All substantive information
provided during the comment period
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has either been incorporated directly
into this final determination or is
addressed below.
Peer Review
In accordance with our peer review
policy published on July 1, 1994 (59 FR
34270), we solicited expert opinion
from 12 knowledgeable individuals with
scientific expertise that included
familiarity with the 5 species and their
habitats, biological needs, and threats.
We received responses from four of the
peer reviewers.
We reviewed all comments received
from the peer reviewers for substantive
issues and new information regarding
the listing of the five fishes. The peer
reviewers generally concurred with our
conclusions and provided additional
information on taxonomic classification,
life-history, and distribution; technical
clarifications; and suggestions to
improve the final rule. Peer reviewer
comments are addressed in the
‘‘Summary of Changes from Proposed
Rule’’ and incorporated into the final
rule as appropriate.
Public Comments
(1) Comment: Two commenters stated
that the laurel dace is threatened,
particularly in Horn Branch, a tributary
to the Rock Creek watershed, by timber
harvest, rock harvest (collection of
surface fieldstones), and coal mining of
the Sewanee Coal Seam in Bledsoe and
Rhea counties, Tennessee. These
commenters recommended critical
habitat designation in the Upper Rock
Creek watershed of Bledsoe County,
Tennessee, due to the threats that are
imminent and of high magnitude in
Horn Branch. The commenters are
particularly concerned that mining of
the Sewanee Coal Seem would result in
acid mine drainage.
Our Response: We concur with these
commenters that the laurel dace in Rock
Creek watershed is threatened by timber
harvest, rock harvest, and coal mining.
We have incorporated further analyses
regarding the threats of rock harvest and
coal mining under ‘‘Summary of Factors
Affecting the Species’’ for laurel dace.
Further analysis with regard to critical
habitat designation will be addressed in
the upcoming critical habitat rule.
(2) Comment: One commenter stated
that the Cumberland darter is
threatened, particularly in Dan Branch,
a tributary to the Lick Fork watershed,
by degradation of water quality from
mountaintop mining projects in
Campbell and Claiborne counties,
Tennessee. In addition to this general
concern, the commenter was aware of
selenium contamination within these
same watersheds and feared that the
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issuance of new permits would cause
further degradation to fish and wildlife
habitats in Campbell County.
Our Response: We concur with the
commenter that mountaintop mining,
and specifically selenium
contamination, has the potential to
degrade the water quality of
Cumberland darter streams in Campbell
and Claiborne counties, Tennessee.
Streams associated with mountaintop
mining and valley fills are characterized
by increased conductivity, total
dissolved solids, and concentrations of
sulfate, bicarbonate ions, and metals
such as manganese, iron, aluminum,
and selenium. Increased levels of
selenium have been shown to
bioaccumulate in organisms, leading to
deformities in larval fish and potentially
harming birds that prey on fishes. The
proposed rule provided a more detailed
analysis of these and other water quality
threats to the Cumberland darter under
‘‘Summary of Factors Affecting the
Species.’’
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Summary of Changes From Proposed
Rule
As a result of the comments received
during the public comment period (see
above) we made the following changes
to the final listing rule:
(1) We added taxonomic classification
information to the species’ background
sections.
(2) We added life-history information
to the Cumberland darter and chucky
madtom background sections.
(3) We updated the distributional
information for the rush darter in
Alabama.
(4) We changed the genus of laurel
dace from Phoxinus to Chrosomus to
reflect recent taxonomic changes
(Strange and Mayden 2009).
(5) We updated population estimate
and threats information for the
yellowcheek darter in Arkansas.
Summary of Factors Affecting the
Species
Section 4 of the Act and its
implementing regulations (50 CFR 424)
set forth the procedures for adding
species to the Federal Lists of
Endangered and Threatened Wildlife
and Plants. A species may be
determined to be an endangered or
threatened species due to one or more
of the five factors described in section
4(a)(1) of the Act: (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; and (E) other natural or
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manmade factors affecting its continued
existence. Listing actions may be
warranted based on any of the above
threat factors, singly or in combination.
Each of these factors is discussed below.
A. The Present or Threatened
Destruction, Modification, or
Curtailment of Its Habitat or Range
The primary threat to the Cumberland
darter, rush darter, yellowcheek darter,
chucky madtom, and laurel dace is
physical habitat destruction or
modification resulting from a variety of
human-induced impacts such as
siltation, disturbance of riparian
corridors, and changes in channel
morphology (Waters 1995, pp. 2–3;
Skelton 1997, pp. 17, 19; Thomas 2007,
p. 5). The most significant of these
impacts is siltation (excess sediments
suspended or deposited in a stream)
caused by excessive releases of
sediment from activities such as
resource extraction (e.g., coal mining,
silviculture, natural gas development),
agriculture, road construction, and
urban development (Waters 1995, pp. 2–
3; Kentucky Division of Water (KDOW)
2006, pp. 178–185; Skelton 1997, pp.
17, 19; Thomas 2007, p. 5).
Land use practices that affect
sediment and water discharges into a
stream can also increase the erosion or
sedimentation pattern of the stream,
which can lead to the destruction or
modification of in-stream habitat and
riparian vegetation, stream bank
collapse, and increased water turbidity
and temperature. Sediment has been
shown to abrade and suffocate bottomdwelling fish and other organisms by
clogging gills; reduce aquatic insect
diversity and abundance; impair fish
feeding behavior by altering prey base
and reducing visibility of prey; impair
reproduction due to burial of nests; and,
ultimately, negatively impact fish
growth, survival, and reproduction
(Waters 1995, pp. 5–7, 55–62; Knight
and Welch 2001, pp. 134–136). Wood
and Armitage (1997, pp. 211–212)
identified at least five impacts of
sedimentation on fish, including (1)
reduction of growth rate, disease
tolerance, and gill function; (2)
reduction of spawning habitat and egg,
larvae, and juvenile development; (3)
modification of migration patterns; (4)
reduction of food availability through
the blockage of primary production; and
(5) reduction of foraging efficiency. The
effects of these types of threats will
likely increase as development increases
in these watersheds.
Non-point source pollution from land
surface runoff can originate from
virtually any land use activity and may
be correlated with impervious surfaces
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48731
and storm water runoff. Pollutants may
include sediments, fertilizers,
herbicides, pesticides, animal wastes,
septic tank and gray water leakage,
pharmaceuticals, and petroleum
products. These pollutants tend to
increase concentrations of nutrients and
toxins in the water and alter the
chemistry of affected streams such that
the habitat and food sources for species
like the Cumberland darter, rush darter,
yellowcheek darter, chucky madtom,
and laurel dace are negatively impacted.
Construction and road maintenance
activities associated with urban
development typically involve earthmoving activities that increase sediment
loads into nearby streams. Other
siltation sources, including timber
harvesting, natural gas development
activities, clearing of riparian
vegetation, mining, and agricultural
practices, allow exposed earth to enter
streams during or after precipitation
events. These activities result in canopy
removal, elevated stream temperatures,
and increased siltation, thereby
degrading habitats used by fishes for
both feeding and reproduction
(Mattingly et al. 2005, p. 5).
Undisturbed riparian corridors are
important because they prevent elevated
stream temperatures due to solar
heating, serve as buffers against nonpoint source pollutants, provide
submerged root materials for cover and
feeding, and help to stabilize stream
banks (Mattingly et al. 2005, p. 5).
Cumberland Darter
The Cumberland darter’s preferred
habitat characteristics (i.e., low- to
moderate-gradient, low current velocity,
backwater nature) make it extremely
susceptible to the effects of siltation
(O’Bara 1991, p. 11). Sediment
(siltation) has been listed repeatedly by
KDOW as the most common stressor of
aquatic communities in the upper
Cumberland River basin (KDOW 1996,
pp. 50–53, 71–75; KDOW 2002, pp. 39–
40; KDOW 2006, pp. 178–185). The
primary source of sediment was
identified as resource extraction (e.g.,
coal mining, logging). The streams
within the Cumberland darter’s current
range that are identified as impaired
(due to siltation from mining, logging,
and agricultural activities) and have
been included on Kentucky’s 303(d) list
of impaired waters (KDOW 2007, pp.
155–166) include Jenneys Branch
(Indian Creek basin), an unnamed
tributary of Jenneys Branch (Indian
Creek basin), Ryans Creek (Jellico Creek
basin), Marsh Creek, and Wolf Creek
(Clear Fork basin).
Siltation can also occur in the
Cumberland darter’s known habitat as a
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result of construction activities for
human development. For example,
during the fall of 2007, an 8.4-km (5.2mi) reach of Barren Fork in McCreary
County, Kentucky, was subjected to a
severe sedimentation event (Floyd pers.
obs. 2008). This event occurred despite
the fact that approximately 95 percent of
the Barren Fork watershed is under
Federal ownership within the Daniel
Boone National Forest (DBNF).
Construction activities associated with
the development of a 40.5-hectare (100acre) park site caused excessive
sedimentation of two unnamed
headwater tributaries of Barren Fork.
Successive, large rainfall events in
September and October carried
sediment offsite and impacted
downstream areas of Barren Fork known
to support Cumberland darters and the
Federally threatened blackside dace.
Our initial site visit on September 7,
2007, confirmed that sediment had been
carried offsite, resulting in significant
habitat degradation in the Barren Fork
mainstem and ‘‘adverse effects’’ on the
blackside dace. Several smaller
sediment events have occurred despite
Federal and State attempts to resolve the
issue, and on July 31, 2008, another
large rainfall event resulted in excessive
sedimentation in two Barren Fork
watershed streams.
Another significant threat to the
Cumberland darter is water quality
degradation caused by a variety of nonpoint source pollutants. Coal mining
represents a major source of these
pollutants (O’Bara 1991, p. 11; Thomas
2007, p. 5), because it has the potential
to contribute high concentrations of
dissolved metals and other solids that
lower stream pH or lead to elevated
levels of stream conductivity (Pond
2004, pp. 6–7, 38–41; Mattingly et al.
2005, p. 59). These impacts have been
shown to negatively affect fish species,
including listed species, in the Clear
Fork system of the Cumberland basin
(Weaver 1997, pp. 29; Hartowicz pers.
comm. 2008). The direct effect of
elevated stream conductivity on fishes,
including the Cumberland darter, is
poorly understood, but some species,
such as blackside dace, have shown
declines in abundance over time as
conductivity increased in streams
affected by mining (Hartowicz pers.
comm. 2008). Studies indicate that
blackside dace are generally absent
when conductivity values exceed 240
microSiemens (μS) (Mattingly et al.
2005, p. 59; Black and Mattingly 2007,
p. 12).
Other non-point source pollutants
that affect the Cumberland darter
include domestic sewage (through
septic tank leakage or straight pipe
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discharges); agricultural pollutants such
as fertilizers, pesticides, herbicides, and
animal waste; and other chemicals
associated with oil and gas
development. Non-point source
pollutants can cause excess nutrification
(increased levels of nitrogen and
phosphorus), excessive algal growth,
instream oxygen deficiencies, increased
acidity and conductivity, and other
changes in water chemistry that can
seriously impact aquatic species (KDOW
1996, pp. 48–50; KDOW 2006, pp. 70–
73).
In summary, habitat loss and
modification represent significant
threats to the Cumberland darter. Severe
degradation from sedimentation,
physical habitat disturbance, and
contaminants threatens the habitat and
water quality on which the Cumberland
darter depends. Sedimentation from
coal mining, logging, agriculture, and
development sites within the upper
Cumberland basin negatively affect the
Cumberland darter by reducing growth
rates, disease tolerance, and gill
function; reducing spawning habitat,
reproductive success, and egg, larvae,
and juvenile development; modifying
migration patterns; reducing food
availability through reductions in prey;
and reducing foraging efficiency.
Contaminants associated with coal
mining (metals, other dissolved solids),
domestic sewage (bacteria, nutrients),
and agriculture (fertilizers, pesticides,
herbicides, and animal waste) cause
degradation of water quality and
habitats through increased acidity and
conductivity, instream oxygen
deficiencies, excess nutrification, and
excessive algal growths. Furthermore,
these threats faced by the Cumberland
darter from sources of sedimentation
and contaminants are imminent, the
result of ongoing projects that are
expected to continue indefinitely. As a
result of the imminence of these threats
combined with the vulnerability of the
remaining small populations to
extirpation from natural and manmade
threats, we have determined that the
present or threatened destruction,
modification, or curtailment of the
Cumberland darter habitat and range
represents a significant threat of high
magnitude. We have no information
indicating that the magnitude or
imminence of this threat is likely to be
appreciably reduced in the foreseeable
future.
Rush Darter
Sediment is the most abundant
pollutant in the Mobile River Basin
(Alabama Department of Environmental
Management 1996, pp. 14–15) and a
major threat to the rush darter. Within
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the Clear Creek drainage, Johnston and
Kleiner (2001, p. 4) reported that, during
August 2001, the dominant land use
adjacent to Doe Branch and Mill Creek
appeared to be forests, and that there
were no obvious threats to water
quality. However, Johnston and Kleiner
(2001, p. 4) reported that clearcutting in
the Wildcat Branch watershed may have
increased sedimentation into the stream.
Approximately 84 percent (i.e., 5 km or
3 mi) of Wildcat Branch is privately
owned, and recent land exchanges
within the Bankhead National Forest
have taken about 0.9 km (0.6 mi) of
stream west of Clear Creek out of U.S.
Forest Service (USFS) management and
protection. In 2001, Service and USFS
personnel noted heavy siltation at the
County Road 329 Bridge over Doe
Branch and at several other road
crossings in other tributary streams in
the immediate area during a modest
spring rain event. Sediment in area
streams is also the result of increased
erosion from the scouring of roadside
ditches, and erosion of the gravel
County Road 329 itself adjacent to Doe
and Wildcat branches (Drennen pers.
obs. 2005).
Blanco (2001, p. 68) identified
siltation from development projects as
the greatest threat to the fauna of Turkey
Creek. New subdivisions have been
developed throughout the watershed,
increasing the amount of impervious
surfaces in the recharge areas of springs.
The increase in impervious surfaces is
leading to increased stormwater runoff
and is reducing the amount of recharge
(water storage) available to the aquifers
that feed springs in the watershed.
These flow alterations reduce the
amount and complexity of rush darter
habitat by eroding stream banks,
destabilizing substrates and aquatic
vegetation, and decreasing overall water
quality.
There are four major soil types that
occur within the Turkey Creek
watershed, and all are considered highly
erodible due to the steep topography
(Spivey 1982, pp. 5, 7, 8, 14). Therefore,
any activity that removes native
vegetation on these soils can be
expected to lead to increased sediment
loads in Turkey Creek watershed
(USFWS 2001, p. 59370), including the
areas near Penny and Tapawingo
Springs. Industrialization is extensive
and expanding throughout the
watershed, particularly near the type
locality for the rush darter (Bart and
Taylor 1999, p. 33; Drennen pers. obs.
2007–2010).
Point source siltation has impacted
the Turkey Creek watershed, including
an abundance of sites affecting Beaver
Creek, a major tributary to Turkey
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Creek. These sites are impaired by
bridge, road, and sewer line
construction; industrialized areas; road
maintenance; and storm water
mismanagement (Drennen pers. obs.
1999, 2004–2010). Rapid urbanization
in this area renders this population
extremely vulnerable during the
breeding season when rush darters
concentrate in wetland pools and
shallow pools with aquatic vegetation in
headwater streams (Stiles and Mills
2008, p. 5; Fluker et al. 2007, p. 10).
Springs throughout the rush darter’s
range, especially in Pinson Valley, flush
and dilute sediments and excessive
nutrients from streams by providing a
constant flow of cool, clean water.
However, the ongoing destruction of
spring heads and wetlands throughout
the species’ range has significantly
reduced the species’ movement and
colonization. Little Cove Creek and
Bristow Creek spring heads have been
channelized, and the head of Cove
Spring has a pumping facility built on
it (Fluker et al. 2007, p. 1).
Channelization and groundwater
withdrawals from spring heads might do
more to impact water quality in these
systems than overall spring drainage
disturbances such as beaver dam
construction, and road maintenance
(Drennen per. obs. 2005). Alteration of
spring head habitats has reduced water
quality and increased sediment loads
into spring-fed tributary streams
throughout the range of the rush darter.
In summary, threats to rush darter
include stormwater runoff and siltation,
caused by an increase in urbanization
and impervious surfaces in the
watershed. Other threats include spring
head alteration, roadside maintenance,
and logging. These threats are ongoing
and thus considered imminent. The
magnitude of the threats is high due to
the small population sizes and high
levels of alterations and destruction of
the springs and streams. We have no
information indicating that the
magnitude or imminence of these
threats is likely to be appreciably
reduced in the foreseeable future.
Yellowcheek Darter
Robison and Harp (1981, p. 17),
McDaniel (1984, p. 92), and Robison
and Buchanan (1988, p. 429) have
attributed the decline in populations of
yellowcheek darters in the four forks of
the Little Red River and the mainstem
Little Red River to habitat alteration and
degradation. The suspected primary
cause of the species’ decline is the
impoundment of the Little Red River
and lower reaches of the Devils, Middle,
and South Forks, areas that in the past
provided optimal habitat for this
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species. The creation of Greers Ferry
Lake, in 1962, converted optimal
yellowcheek darter habitat (clear, cool,
perennial flow with large substrate
particle size (Robison and Buchanan
1988, p. 429)), to a deep, standing water
environment. This dramatic change in
habitat flooded spawning sites and
changed chemical and physical
characteristics in the streams that
provide habitat for the species.
Impoundments profoundly alter
channel characteristics, habitat
availability, and flow regime with
serious consequences for biota (Allan
and Flecker 1993, p. 36, Ward and
Stanford 1995, pp. 105–119). Some of
these include converting flowing to still
waters, increasing depths and
sedimentation, decreasing dissolved
oxygen, drastically altering resident fish
populations (Neves et al. 1997, p. 63),
disrupting fish migration, and
destroying spawning habitat (Ligon et
al. 1995, pp. 185–86). Channelization of
the lower 5.6 km (3.5 miles) of Archey
and South Forks in 1985 and
subsequent, and ongoing, channel
maintenance by the U.S. Army Corps of
Engineers (USACE) and City of Clinton,
Arkansas, degraded habitat in this reach
as well as segments upstream of the
project area. Based upon current
knowledge and a 2004–2005 threats
assessment (Davidson and Wine 2004,
pp. 6–13; Davidson 2005, pp. 1–4),
gravel mining, unrestricted cattle access
into streams, water withdrawal for
agricultural and recreational purposes
(i.e., golf courses), lack of adequate
riparian buffers, construction and
maintenance of county roads, and nonpoint source pollution arising from a
broad array of activities also appear to
be degrading suitable habitat for the
species. The threats assessment
documented occurrences of the
aforementioned activities and found 52
sites on the Middle Fork, 28 sites on the
South Fork, 8 sites on Archey Fork
(Davidson 2005, pp. 1–4), and 1 site in
the Turkey/Beech/Devils Fork system
that are adversely affected by these
activities and are likely contributors to
the decline of the species.
Ozark headwater streams typically
exhibit seasonal fluctuations in flows,
with flow rates highest in spring and
lowest in late summer and fall. The
upper reaches of these small streams are
most affected by seasonally fluctuating
water levels (Robison and Harp 1981, p.
17). As a result, they often lack
consistent and adequate flows, and by
late summer or fall are reduced to a
series of isolated pools (Wine pers.
comm. 2008). Expanding natural gas
development activities that began in the
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upper Little Red River watershed in
2006 require large quantities of water
(both surface water and groundwater)
and pose an imminent threat to the
continued existence of yellowcheek
darter as these activities rapidly expand
and increase in the watersheds of all
four forks (Davidson pers. comm. 2008).
Because the yellowcheek darter requires
permanent flows with moderate to
strong current (Robison and Buchanan
1988, p. 429), and because downstream
refugia have been lost to impoundments
and channelization, water withdraws
that exacerbate seasonal stream
reductions and reduce moving water
(lotic) habitat are a serious threat.
Additional threats to the yellowcheek
darter include habitat degradation from
land use activities in the watershed,
including agriculture and forestry.
Traditional farming practices, feedlot
operations, and associated poor land use
practices contribute many pollutants to
rivers. Neves et al. (1997, p. 65) suggest
that agriculture affects 72 percent of
impaired river reaches in the United
States. Nutrients, bacteria, pesticides,
and other organic compounds generally
are found in higher concentrations in
agricultural areas than forested areas.
Nutrient concentrations in streams may
result in increased algal growth in
streams, and a related alteration in fish
community composition (Petersen et al.
1999, p. 16). Major agricultural activities
within the Little Red River watershed
include poultry, dairy, swine, and beef
cattle operations.
The Arkansas Natural Resources
Conservation Service (NRCS) has
identified animal wastes, nutrients,
excessive erosion, loss of plant
diversity, and loss of species as water
quality concerns associated with
agricultural land use activities in the
upper Little Red River watershed (NRCS
1999). Large poultry and dairy
operations increase nutrient inputs to
streams when producers apply animal
waste to pastures to stimulate vegetation
growth for grazing and hay production.
Continuous grazing methods in the
watershed allow unrestricted animal
access to grazing areas, and on steeper
slopes this results in increased runoff
and erosion (NRCS 1999). Since
pastures often extend directly to the
edge of the stream, and lack a riparian
zone with native vegetation, runoff from
pastures carries pollutants directly into
streams. Eroding stream banks also
result in alterations to stream hydrology
and geomorphology, degrading habitat.
Livestock spend a disproportionate
amount of time in riparian areas during
hot summer months. Trampling and
grazing can change and reduce
vegetation and eliminate riparian areas
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by channel widening, channel
aggradation, or lowering of the water
table (Armour et al. 1991, pp. 7–11).
Additionally, earthen dams were
constructed across a riffle in the lower
South Fork to create a pool for annual
chuckwagon races for many years
leading up to 2003. The Service and
U.S. Army Corps of Engineers met with
the responsible landowner in 2004 and
suggested an alternative to dam
construction that would minimize
impacts to the yellowcheek darter.
These recommendations were followed
for several years; however, another
earthen dam was constructed in 2008
using material from the South Fork to
facilitate events associated with the
annual chuckwagon races. This dam,
like its predecessors, was unpermitted
and resulted in habitat degradation and
alteration for several miles upstream
and downstream of the site.
The chuckwagon race event draws
approximately 20,000 to 30,000 people
per year to the South Fork Little Red
River for a 1-week period around Labor
Day. Horses and wagons traverse the
river and its tributaries for miles leading
to increased habitat disturbance,
sedimentation, and trampling. The
chuckwagon races continue to grow
annually and pose a threat to the
continued existence of yellowcheek
darters in the South Fork Little Red
River.
Timber harvesting activities involving
clear-cutting entire steep hillsides were
observed during 1999–2000 in the
Devils Fork watershed (Wine pers.
comm. 2008). The failure to implement
voluntary State best management
practices (BMPs) for intermittent and
perennial streams during timber
harvests has resulted in water quality
degradation and habitat alteration in
stream reaches adjacent to harvesting
operations. When timber harvests
involve clear cutting to the water’s edge,
without leaving a riparian buffer, silt
and sediment enter streams lying at the
bottom of steep slopes. The lack of
streamside vegetation also promotes
bank erosion that alters stream courses
and introduces large quantities of
sediment into the channel (Allan 1995,
p. 321). Timber harvest operations that
use roads on steep slopes to transport
timber can carry silt and sediment from
the road into the stream at the bottom
of the slope. Logging impacts on
sediment production are considerable,
but often erosion of access and haul
roads produces more sediment than the
land harvested for timber (Brim Box and
Mossa 1999, p. 102). These activities
have occurred historically and continue
to occur in the upper Little Red River
watershed.
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Natural gas exploration and
development is a newly emerging threat
to yellowcheek darter populations.
Erosion and sedimentation issues
associated with natural gas development
activities, particularly pipelines (herein
defined as all flow lines, gathering lines,
and non-interstate pipelines), were first
documented by Service biologists
during 2007 in the South Fork Little Red
River watershed. In June 2008, the
Service began documenting significant
erosion and sedimentation issues
associated with natural gas pipeline
construction and maintenance as
natural gas development activities
expanded into the watershed. Service
biologists documented erosion and
sedimentation at almost every new
pipeline stream crossing in the South
Fork and Middle Fork Little Red River
watersheds, regardless of the diameter
of the pipe. Channel incision was
documented at numerous stream
crossings that are tributaries to the
South Fork Little Red River. The
incision increased erosion and
sedimentation, as well as altering the
hydrology and geomorphology
characteristics of the streams. Pipeline
rights-of-way were found to have one of
the following conditions: (1) No BMPs
(i.e., silt fences, grade breaks, nonerodible stream crossing materials)
installed to prevent erosion and
sedimentation; (2) ineffective erosion
minimization practices in place; (3)
effective erosion minimization practices
that had not been maintained and, thus,
had become ineffective; or (4) final
reclamation of the pipeline right-of-way
had not occurred for months and in
some cases greater than a year after
construction activities ceased, leading to
prolonged periods of erosion and
sedimentation. The magnitude of the
impacts to the South Fork and Middle
Fork Little Red River from 2007–2008
also was exacerbated due to aboveaverage rainfall, which led to more
frequent and larger pipeline erosion
events.
In summary, threats to the
yellowcheek darter from the present
destruction, modification, or
curtailment of its habitat or range
negatively impact the species. Threats
include such activities as
impoundment, sedimentation, poor
livestock grazing practices, improper
timber harvest practices, nutrient
enrichment, gravel mining,
channelization/channel instability, and
natural gas development. These threats
are considered imminent and of high
magnitude throughout the species’
entire range. We have no information
indicating that the magnitude or
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imminence of these threats is likely to
be appreciably reduced in the
foreseeable future, and in the case of
pipeline disturbance, we expect this
threat to become more problematic over
the next several years as natural gas
development continues to intensify.
Chucky Madtom
The current range of the chucky
madtom is believed to be restricted to an
approximately 1.8-mi (3-km) reach of
Little Chucky Creek in Greene County,
Tennessee. Land use data from the
Southeast GAP Analysis Program (SE–
GAP) show that land use within the
Little Chucky Creek watershed is
predominantly agricultural, with the
vast majority of agricultural land being
devoted to production of livestock and
their forage base (Jones et al. 2000).
Traditional farming practices, feedlot
operations, and associated land use
practices contribute many pollutants to
rivers. Neves et al. (1997, p. 65) suggest
that agriculture affects 72 percent of
impaired river reaches in the United
States. These practices erode stream
banks and result in alterations to stream
hydrology and geomorphology,
degrading habitat. Nutrients, bacteria,
pesticides, and other organic
compounds generally are found in
higher concentrations in agricultural
areas than forested areas. Nutrient
concentrations in streams may result in
increased algal growth in streams, and
a related alteration in fish community
composition (Petersen et al. 1999, p.
16).
The TVA Index of Biological Integrity
results indicate that Little Chucky Creek
is biologically impaired (Middle
Nolichucky Watershed Alliance 2006, p.
13). Given the predominantly
agricultural land use within the Little
Chucky Creek watershed, non-point
source sediment and agrochemical
discharges may pose a threat to the
chucky madtom by altering the physical
characteristics of its habitat, thus
potentially impeding its ability to feed,
seek shelter from predators, and
successfully reproduce. The Little
Chucky Creek watershed also contains a
portion of the City of Greeneville,
providing an additional source for input
of sediments and contaminants into the
creek and threatening the chucky
madtom. Wood and Armitage (1997, pp.
211–212) identify at least five impacts of
sedimentation on fish, including (1)
reduction of growth rate, disease
tolerance, and gill function; (2)
reduction of spawning habitat and egg,
larvae, and juvenile development; (3)
modification of migration patterns; (4)
reduction of food availability through
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the blockage of primary production; and
(5) reduction of foraging efficiency.
The chucky madtom is a bottomdwelling species. Bottom-dwelling fish
species are especially susceptible to
sedimentation and other pollutants that
degrade or eliminate habitat and food
sources (Berkman and Rabeni 1987, pp.
290–292; Richter et al. 1997, p. 1091;
Waters 1995, p. 72). Etnier and Jenkins
(1980, p. 20) suggested that madtoms,
which are heavily dependent on
chemoreception (detection of chemicals)
for survival, are susceptible to humaninduced disturbances, such as chemical
and sediment inputs, because the
olfactory (sense of smell) ‘‘noise’’ they
produce could interfere with a
madtom’s ability to obtain food and
otherwise monitor its environment.
In summary, threats to the chucky
madtom from the present destruction,
modification, or curtailment of its
habitat or range negatively impact the
species. Degradation from
sedimentation, physical habitat
disturbance, and contaminants threaten
the habitat and water quality on which
the chucky madtom depends.
Sedimentation from agricultural lands
could negatively affect the chucky
madtom by reducing growth rates,
disease tolerance, and gill function;
reducing spawning habitat, reproductive
success, and egg, larvae, and juvenile
development; reducing food availability
through reductions in prey; and
reducing foraging efficiency.
Contaminants associated with
agriculture (e.g., fertilizers, pesticides,
herbicides, and animal waste) can cause
degradation of water quality and
habitats through instream oxygen
deficiencies, excess nutrification, and
excessive algal growths. Furthermore,
these threats faced by the chucky
madtom from sources of sedimentation
and contaminants are imminent; the
result of ongoing agricultural practices
that are expected to continue
indefinitely. As a result of the
imminence of these threats combined
with the vulnerability of the remaining
small population to extirpation from
natural and manmade threats, we have
determined that the present or
threatened destruction, modification, or
curtailment of the chucky madtom
habitat and range represents a
significant threat of high magnitude. We
have no information indicating that the
magnitude or imminence of these
threats is likely to be appreciably
reduced in the foreseeable future.
Laurel Dace
Skelton (2001, p. 127) concluded that
the laurel dace is ‘‘presumably tolerant
of some siltation.’’ However, Strange
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and Skelton (2005, p. 7 and Appendix
2) observed levels of siltation they
considered problematic during later
surveys for the laurel dace and
concluded this posed a threat in several
localities throughout the range of the
species. Sediment has been shown to
abrade and or suffocate bottom-dwelling
fish and other organisms by clogging
gills; reducing aquatic insect diversity
and abundance; impairing fish feeding
behavior by altering prey base and
reducing visibility of prey; impairing
reproduction due to burial of nests; and,
ultimately, negatively impacting fish
growth, survival, and reproduction
(Waters 1995, pp. 5–7, 55–62; Knight
and Welch 2001, pp. 134–136).
However, we do not currently know
what levels of siltation laurel dace are
able to withstand before populations
begin to decline due to these siltationrelated stressors. The apparent stability
of the northern population of laurel
dace in the Piney River system suggests
that this species is at least moderately
tolerant of siltation-related stressors. We
do not know the extent to which other
factors might have driven the decline of
the southern populations in Sale and
Soddy Creeks.
Of the streams inhabited by the
southern populations recognized by
Strange and Skelton (2005, p. Appendix
2), the reaches from which laurel dace
have been collected in Soddy Creek and
Horn Branch approach 1 km (0.6 mi) in
length. In Cupp Creek, collections of
this species are restricted to less than
300 m (984 ft) of stream, in spite of
surveys well beyond the reach known to
be inhabited. In each of the streams
occupied by the southern populations,
Strange and Skelton (2005, Appendix 2)
identified siltation as a factor that could
alter the habitat and render it unsuitable
for laurel dace. The restricted
distribution of laurel dace in streams
inhabited by the southern populations
leaves them highly vulnerable to
potential deleterious effects of excessive
siltation or other localized disturbances.
A newly emerging threat to laurel
dace in Soddy Creek is the conversion
of silvicultural lands to row crop
agriculture. Two large pine plantations
within the Soddy Creek Watershed were
harvested and then converted to tomato
farms. An irrigation impoundment was
built on one Soddy Creek tributary and
another is under construction. As a
result of these activities, a large silt
source was introduced into the Soddy
Creek headwaters. In addition to
contributing sediment, crop fields often
allow runoff from irrigation water to
flow directly into the creek. This water
contains fungicides, herbicides, and
fertilizers (Thurman pers. comm. 2010).
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Strange and Skelton (2005, p. 7 and
Appendix 2) identified siltation as a
threat in all of the occupied Piney River
tributaries (Young’s, Moccasin, and
Bumbee Creeks). The Bumbee Creek
type locality for the laurel dace is
located within industrial forest that has
been subjected to extensive clear-cutting
and road construction in close
proximity to the stream. Strange and
Skelton (2005, p. 7) noted a heavy
sediment load at this locality and
commented that conditions in Bumbee
Creek in 2005 had deteriorated since the
site was visited by Skelton in 2002.
Strange and Skelton (2005, pp. 7 and 8
and Appendix 2) also commented on
excessive siltation in localities they
sampled on Young’s and Moccasin
Creeks, and observed localized removal
of riparian vegetation around residences
in the headwaters of each of these
streams. They considered the removal of
riparian vegetation problematic not only
for the potential for increased siltation,
but also for the potential thermal
alteration of these small headwater
streams. Skelton (2001, p. 125) reported
that laurel dace occupy cool streams
with a maximum recorded temperature
of 26 °C (78.8 °F). The removal of
riparian vegetation could potentially
increase temperatures above the laurel
dace’s maximum tolerable limit.
Water temperature may be a limiting
factor in the distribution of this species
(Skelton 1997, pp. 17, 19). Canopy cover
of laurel dace streams often consists of
eastern hemlock (Tsuga canadensis),
mixed hardwoods, pines (Pinus spp.),
and mountain laurel (Kalmia latifolia).
The hemlock woolly adelgid (Adelges
tsugae) is a nonnative insect that infests
hemlocks, causing damage or death to
trees. The woolly adelgid was recently
found in Hamilton County, Tennessee,
and could impact eastern hemlock in
floodplains and riparian buffers along
laurel dace streams in the future
(Simmons pers. comm. 2008). Riparian
buffers filter sediment and nutrients
from overland runoff, allow water to
soak into the ground, protect stream
banks, and provide shade for streams
(Waters 1995, p. 149–152). Because
eastern hemlock is primarily found in
riparian areas, the loss of this species
adjacent to laurel dace streams would be
detrimental to fish habitat.
Habitat destruction and modification
also stem from existing or proposed
infrastructure development in
association with silvicultural activities.
The presence of culverts at one or more
road crossings in most of the streams
inhabited by laurel dace may disrupt
upstream dispersal within those systems
(Chance pers. obs. 2008). Such dispersal
barriers could prevent re-establishment
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of laurel dace populations in reaches
where they suffer localized extinctions
due to natural or human-caused events.
In summary, the primary threat to
laurel dace throughout its range is
excessive siltation resulting from
agriculture and extensive silviculture
involving both inadequate riparian
buffers in harvest areas and the failure
to use BMPs during road construction.
Severe degradation from sedimentation,
physical habitat disturbance, and
contaminants threatens the habitat and
water quality on which the laurel dace
depends. Sedimentation negatively
affects species (such as the laurel dace)
by reducing growth rates, disease
tolerance, and gill function; reducing
spawning habitat, reproductive success,
and egg, larvae, and juvenile
development; reducing food availability
through reductions in prey; and
reducing foraging efficiency (Waters
1995, pp. 5–7; 55–62; Wood and
Armitage 1997, pp. 211–212; Knight and
Welch 2001, pp. 134–136). These threats
faced by the laurel dace from sources of
sedimentation and contaminants are
imminent, the result of ongoing
agricultural and silvicultural practices
that are expected to continue. Since the
identified threats substantially affect
survival, growth, reproduction, and
feeding, we have determined that the
present or threatened destruction,
modification, or curtailment of the
laurel dace habitat and range represents
a significant threat of high magnitude.
We have no information indicating that
the magnitude or imminence of these
threats is likely to be appreciably
reduced in the foreseeable future.
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B. Overutilization for Commercial,
Recreational, Scientific, or Educational
Purposes
The Cumberland darter, rush darter,
yellowcheek darter, chucky madtom,
and laurel dace are not commercially
utilized. Individuals have been taken for
scientific and private collections in the
past, but collecting is not considered a
factor in the decline of these species and
is not expected to be so in the future.
The available information does not
indicate that overutilization is likely to
become a threat to any of these five
fishes in the foreseeable future.
C. Disease or Predation
Disease is not considered to be a
factor in the decline of the Cumberland
darter, rush darter, yellowcheek darter,
chucky madtom, or laurel dace.
Although the Cumberland darter, rush
darter, yellowcheek darter, and laurel
dace are undoubtedly consumed by
predators, the available information
suggests that this predation is naturally
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occurring, or a normal aspect of the
population dynamics. As a result, we do
not believe that predation is considered
to currently pose a threat to these
species. Furthermore, the information
we do have does not indicate that
disease or predation is likely to become
a threat to any of these five fishes in the
foreseeable future.
D. The Inadequacy of Existing
Regulatory Mechanisms
Cumberland Darter
The Cumberland darter and its
habitats are afforded some protection
from water quality and habitat
degradation under the Clean Water Act
of 1977 (33 U.S.C. 1251 et seq.),
Kentucky’s Forest Conservation Act of
1998 (KRS 149.330–355), Kentucky’s
Agriculture Water Quality Act of 1994
(KRS 224.71–140), additional Kentucky
laws and regulations regarding natural
resources and environmental protection
(KRS 146.200–360; KRS 224; 401 KAR
5:026, 5:031), and Tennessee’s Water
Quality Control Act of 1977 (TWQCA;
T.C.A. 69–3–101). However, as
demonstrated under Factor A,
population declines and degradation of
habitat for this species are ongoing
despite the protection afforded by these
laws and corresponding regulations.
While these laws have resulted in some
improvements in water quality and
stream habitat for aquatic life, including
the Cumberland darter, they alone have
not been adequate to fully protect this
species; sedimentation and non-point
source pollutants continue to be a
significant problem.
States maintain water-use
classifications through issuance of
National Pollutant Discharge
Elimination System (NPDES) permits to
industries, municipalities, and others.
NPDES permits set maximum limits on
certain pollutants or pollutant
parameters. For water bodies on the
303(d) list, States are required under the
Clean Water Act to establish a total
maximum daily load (TMDL) for the
pollutants of concern that will bring
water quality into the applicable
standard. Three Cumberland darter
streams, Jenneys Branch, Marsh Creek,
and Wolf Creek, have been identified as
impaired by the KDOW and placed on
the State’s 303(d) list (KDOW 2008).
Causes of impairment were listed as
siltation/sedimentation from
agriculture, coal mining, land
development, and silviculture and
organic enrichment/eutrophication from
residential areas. TMDLs have not yet
been developed for these pollutants.
The Cumberland darter has been
designated as an endangered species by
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Tennessee (TWRA 2005, p. 240) and
Kentucky (KSNPC 2005, p. 11), but the
designation in Kentucky conveys no
legal protection. Under the Tennessee
Nongame and Endangered or
Threatened Wildlife Species
Conservation Act of 1974 (Tennessee
Code Annotated §§ 70–8–101–112), ‘‘[I]t
is unlawful for any person to take,
attempt to take, possess, transport,
export, process, sell or offer for sale or
ship nongame wildlife, or for any
common or contract carrier knowingly
to transport or receive for shipment
nongame wildlife.’’ Further, regulations
included in the Tennessee Wildlife
Resources Commission Proclamation
00–15 Endangered Or Threatened
Species state the following: ‘‘Except as
provided for in Tennessee Code
Annotated, Section 70–8–106 (d) and
(e), it shall be unlawful for any person
to take, harass, or destroy wildlife listed
as threatened or endangered or
otherwise to violate terms of Section
70–8–105 (c) or to destroy knowingly
the habitat of such species without due
consideration of alternatives for the
welfare of the species listed in (1) of this
proclamation, or (2) the United States
list of Endangered fauna.’’ Under these
regulations, potential collectors of this
species are required to have a State
collection permit, therefore protecting
against potential threats under Factor B.
However, in terms of project
management, and potential habitat
disturbance, this regulation only
provides for the consideration of
alternatives, and does not require the
level of project review afforded by the
Act.
In 7 of 12 streams where the
Cumberland darter still occurs, the
species receives incidental protection
under the Act due to the coexistence of
the Federally threatened blackside dace.
These streams are in watersheds that are
at least partially owned by the Federal
Government (i.e., DBNF). The five
remaining streams supporting
populations of the Cumberland darter
are not afforded this protection.
In summary, population declines and
degradation of habitat for the
Cumberland darter are ongoing despite
the protection afforded by State and
Federal laws and corresponding
regulations. Because of the vulnerability
of the small remaining populations of
the Cumberland darter and the
imminence of these threats, we find the
inadequacy of existing regulatory
mechanisms to be a significant threat of
high magnitude. Further, the
information available to us at this time
does not indicate that the magnitude or
imminence of this threat is likely to be
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appreciably reduced in the foreseeable
future.
Rush Darter
The rush darter and its habitats are
afforded some protection from water
quality and habitat degradation under
the Clean Water Act and the Alabama
Water Pollution Control Act, as
amended, 1975 (Code of Alabama,
§§ 22–22–1 to 22–22–14). However, as
demonstrated under Factor A,
population declines and degradation of
habitat for this species are ongoing
despite the protection afforded by these
laws. While these laws have resulted in
some improvement in water quality and
stream habitat for aquatic life, including
the rush darter, they alone have not
been adequate to fully protect this
species; stormwater mismanagement,
sedimentation, and non-point source
pollutants continue to be a significant
problem. In addition, these laws have
not adequately addressed water quantity
issues that are a problem throughout the
range of the species. Sediment is the
most abundant pollutant in the Mobile
River Basin and is among the greatest
threats to the rush darter.
The State of Alabama maintains
water-use classifications through
issuance of NPDES permits to
industries, municipalities, and others
that set maximum limits on certain
pollutants or pollutant parameters. For
water bodies on the 303(d) list, States
are required under the Clean Water Act
to establish a TMDL for the pollutants
of concern that will bring water quality
into the applicable standard. The State
of Alabama has not identified any
impaired water bodies in Jefferson,
Winston, and Etowah counties in the
immediate or upstream portion of the
rush darter range or in any watersheds
in Winston or Etowah counties.
However, sedimentation events are
usually related to stormwater runoff
episodes, and are usually not captured
by routine water quality sampling.
Although stormwater events are
temporary in nature, they are still
harmful to aquatic species. The size and
frequency of floods and stormwater
events increases with urbanization
(Konrad 2003, pp. 1–4). Stormwater
events in urban areas decrease the
storage capacity for water in urban
basins compared to rural basins; and
urbanization promotes more rapid
runoff, higher peak discharge rates, and
total volume of water (Konrad 2003, pp.
1–4). Not only does urbanization and
associated runoff change the physical
aspects of water resources, but also the
chemical and biological conditions of
waterways (AMEC Earth and
Environmental 2001, p. 1). Jefferson
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County, Alabama (2005, pp. 2, 39) has
noted that the expansion of impervious
surfaces in the Turkey Creek Drainage
Basin caused an increase in flood
heights and water velocity during
stormwater events. Due to these
observations, the Storm Water
Management Authority and Jefferson
County Department of Health (2010, pp.
4–9) are tracking and monitoring
construction and maintenance sites that
impact stormwater management within
the Turkey Creek and City of Pinson
area. As demonstrated under Factor A,
flow alterations associated with
stormwater runoff reduce the amount
and complexity of rush darter habitat by
eroding stream banks, destabilizing
substrates and aquatic vegetation, and
decreasing overall water quality.
In summary, population declines and
degradation of habitat for the rush darter
are ongoing despite the protection
afforded by State and Federal laws and
corresponding regulations. Despite these
laws, sedimentation, flow alterations,
and non-point source pollution
continue to adversely affect the species.
Because of the vulnerability of the small
remaining populations of the rush darter
and the imminence of these threats, we
find the inadequacy of existing
regulatory mechanisms to be a
significant threat of high magnitude.
Further, the information available to us
at this time does not indicate that the
magnitude or imminence of this threat
is likely to be appreciably reduced in
the foreseeable future.
Yellowcheek Darter
The Arkansas Department of
Environmental Quality (ADEQ) has
established water quality standards for
surface waters in Arkansas, including
specific standards for those streams
designated as ‘‘extraordinary resource
waters’’ (ERW) based on ‘‘a combination
of the chemical, physical, and biological
characteristics of a waterbody and its
watershed, which is characterized by
scenic beauty, aesthetics, scientific
values, broad scope recreation potential,
and intangible social values’’ (ADEQ
Regulation 2, November 25, 2007). As
described in ADEQ’s Regulation 2,
Section 2.203, ERW ‘‘shall be protected
by (1) water quality controls, (2)
maintenance of natural flow regime, (3)
protection of in stream habitat, and (4)
pursuit of land management protective
of the watershed.’’ This regulatory
mechanism has precluded most largescale commercial gravel mining in the
Little Red River watershed; however,
illegal gravel mining is still considered
a cause of habitat degradation and a
threat in this watershed. The Middle,
Archey, and Devils (and its major
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48737
tributaries) forks are designated as ERW.
The South Fork has not been designated
as an ERW. The applicable water quality
standards have not protected
yellowcheek darter habitat from
alterations and water quality
degradation from traditional land use
and expanding natural gas development
activities.
The Arkansas Forestry Commission is
the State agency responsible for
establishing BMPs for timber harvests in
Arkansas. BMPs for timber harvests in
Arkansas are only recommendations;
there is no requirement that timber
harvesters include BMPs in timber
operations. The BMPs are currently
under revision, but the Service does not
know what effect these revisions will
have on aquatic habitats within the
range of the species.
Natural gas production in the upper
Little Red River watershed presents a
unique problem for yellowcheek darter
conservation. In Arkansas, mineral
rights for properties supersede the
surface rights. Even where private
landowners agree to implement certain
BMPs or conservation measures on their
lands for yellowcheek darter
conservation, there is no guarantee that
these BMPs or conservation measures
will be implemented by natural gas
companies, their subsidiaries, or
contractors that lease and develop the
mineral rights for landowners. For this
reason, the intended benefits of
conservation measures agreed to by
landowners in agreements such as
Candidate Conservation Agreements
with Assurances may never be realized.
Additionally, natural gas projects often
do not contain a Federal nexus that
would allow the Service to comment on
proposed or ongoing projects.
The Arkansas Natural Resources
Commission regulates water withdrawal
in Arkansas streams. To date, they have
not precluded water withdrawal for
natural gas development activities in the
upper Little Red River watershed. The
USACE regulates instream activities
under the Clean Water Act. Their policy
to date has been to issue permits for
instream activities associated with
pipeline construction and maintenance
under Nationwide Permits rather than
Individual Permits that require more
public involvement. The ADEQ lacks
the resources necessary to enforce
existing regulations under the Clean
Water Act and the Arkansas Water and
Air Pollution Act for activities
associated with natural gas
development.
The yellowcheek darter receives
incidental protection under the Act due
to the coexistence of the Federally
endangered speckled pocketbook
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mussel (Lampsilis streckeri), which
occurs throughout the upper Little Red
River drainage. However, this protection
has been insufficient to mitigate the
threats to either species.
In summary, the threats of inadequacy
of existing regulatory mechanisms are
imminent and considered high in
magnitude. This is of particular concern
in regard to the vulnerability of the
species to threats from natural gas
development, which is already
impacting populations in the South and
Middle forks of the Little Red River and
is expected to intensify in the next
several years throughout the range of the
species. Further, the information
available to us at this time does not
indicate that the magnitude or
imminence of this threat is likely to be
appreciably reduced in the foreseeable
future.
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Chucky Madtom
The chucky madtom and its habitats
are afforded some protection from water
quality and habitat degradation under
the Clean Water Act and TDEC’s
Division of Water Pollution Control
under the TWQCA. However, as
demonstrated under Factor A,
population declines and degradation of
habitat for this species are ongoing
despite the protection afforded by these
laws. While these laws have resulted in
improved water quality and stream
habitat for aquatic life, including the
chucky madtom, they alone have not
been adequate to fully protect this
species; sedimentation and non-point
source pollutants continue to be a
significant problem. Sediment is the
most abundant pollutant in the Little
Chucky Creek watershed and is the
greatest threat to the chucky madtom.
Portions of the Nolichucky River and
its tributaries in Greene County,
Tennessee, are listed as impaired (303d)
by the State of Tennessee due to pasture
grazing, irrigated crop production,
unrestricted cattle access, land
development, municipal point source
discharges, septic tank failures, gravel
mining, agriculture, and channelization
(TDEC 2010, pp. 64–73). However, Little
Chucky Creek is not listed as ‘‘an
impaired water’’ by the State of
Tennessee (TDEC 2010, pp. 64–73). For
water bodies on the 303(d) (impaired)
list, States are required under the Clean
Water Act to establish a TMDL for the
pollutants of concern that will bring
water quality into the applicable
standard. The TDEC has developed
TMDLs for the Nolichucky River
watershed to address the problems of
fecal coliform loads, siltation, and
habitat alteration by agriculture.
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The chucky madtom receives
incidental protection under the Act due
to the coexistence of the Federally
endangered Cumberland bean (Villosa
trabalis), which is still thought to occur
in Little Chucky Creek, Greene County,
Tennessee (Ahlstedt pers. comm. 2008).
However, this protection has been
insufficient to mitigate the threats to
either species.
The chucky madtom was listed as
Endangered by the State of Tennessee in
September of 2000. Under the
Tennessee Nongame and Endangered or
Threatened Wildlife Species
Conservation Act of 1974 (Tennessee
Code Annotated §§ 70–8–101–112), ‘‘[I]t
is unlawful for any person to take,
attempt to take, possess, transport,
export, process, sell or offer for sale or
ship nongame wildlife, or for any
common or contract carrier knowingly
to transport or receive for shipment
nongame wildlife.’’ Further, regulations
included in the Tennessee Wildlife
Resources Commission Proclamation
00–15 Endangered Or Threatened
Species state the following: ‘‘Except as
provided for in Tennessee Code
Annotated, Section 70–8–106 (d) and
(e), it shall be unlawful for any person
to take, harass, or destroy wildlife listed
as threatened or endangered or
otherwise to violate terms of Section
70–8–105 (c) or to destroy knowingly
the habitat of such species without due
consideration of alternatives for the
welfare of the species listed in (1) of this
proclamation, or (2) the United States
list of Endangered fauna.’’ Under these
regulations, potential collectors of this
species are required to have a State
collection permit. However, in terms of
project management, this regulation
only provides for the consideration of
alternatives, and does not require the
level of project review afforded by the
Act.
In summary, population declines and
degradation of habitat for the chucky
madtom are ongoing despite the
protection afforded by State and Federal
laws and corresponding regulations.
Despite these laws, sedimentation and
non-point source pollution continue to
adversely affect the species. Because of
the vulnerability of the small remaining
populations of the chucky madtom and
the imminence of these threats, we find
the inadequacy of existing regulatory
mechanisms to be a significant threat of
high magnitude. Further, the
information available to us at this time
does not indicate that the magnitude or
imminence of this threat is likely to be
appreciably reduced in the foreseeable
future.
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Laurel Dace
The laurel dace and its habitats are
afforded some protection from water
quality and habitat degradation under
the Clean Water Act and by TDEC’s
Division of Water Pollution Control
under the TWQCA. However, as
demonstrated under Factor A,
population declines and degradation of
habitat for this species are ongoing
despite the protection afforded by these
laws. While these laws have resulted in
improved water quality and stream
habitat for aquatic life, including the
laurel dace, they alone have not been
adequate to fully protect this species;
sedimentation and non-point source
pollutants continue to be a significant
problem. Sediment is the most abundant
pollutant in the watershed and one of
the greatest threats to the laurel dace.
The State of Tennessee maintains
water-use classifications through
issuance of NPDES permits to
industries, municipalities, and others
that set maximum limits on certain
pollutants or pollutant parameters. For
water bodies on the 303(d) list, States
are required under the Clean Water Act
to establish a TMDL for the pollutants
of concern that will bring water quality
into the applicable standard. The TDEC
has not identified any impaired water
bodies in the Soddy Creek, the Sale
Creek system, or the Piney River system
(TDEC 2008).
The TWRA lists the laurel dace as
endangered. Under the Tennessee
Nongame and Endangered or
Threatened Wildlife Species
Conservation Act of 1974 (Tennessee
Code Annotated §§ 70–8–101–112), ‘‘[I]t
is unlawful for any person to take,
attempt to take, possess, transport,
export, process, sell or offer for sale or
ship nongame wildlife, or for any
common or contract carrier knowingly
to transport or receive for shipment
nongame wildlife.’’ Further, regulations
included in the Tennessee Wildlife
Resources Commission Proclamation
00–15 Endangered Or Threatened
Species state the following: ‘‘Except as
provided for in Tennessee Code
Annotated, Section 70–8–106 (d) and
(e), it shall be unlawful for any person
to take, harass, or destroy wildlife listed
as threatened or endangered or
otherwise to violate terms of Section
70–8–105 (c) or to destroy knowingly
the habitat of such species without due
consideration of alternatives for the
welfare of the species listed in (1) of this
proclamation, or (2) the United States
list of Endangered fauna.’’ Under these
regulations, potential collectors of this
species are required to have a State
collection permit. However, in terms of
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project management, this regulation
only provides for the consideration of
alternatives, and does not require the
level of project review afforded by the
Act.
In summary, population declines and
degradation of habitat for the laurel dace
are ongoing despite the protection
afforded by State and Federal water
quality laws. While these laws have
resulted in improved water quality and
stream habitat for aquatic life, including
the laurel dace, they alone have not
been adequate to fully protect this
species; sedimentation and non-point
source pollutants continue to be a
significant problem. Non-point source
pollution is not regulated by the Clean
Water Act. Due to the vulnerability of
the laurel dace to water quality and
habitat degradation, we find the
inadequacy of regulatory mechanisms
that address water quality to be an
imminent threat of high magnitude.
Further, the information available to us
at this time does not indicate that the
magnitude or imminence of this threat
is likely to be appreciably reduced in
the foreseeable future.
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E. Other Natural or Manmade Factors
Affecting Its Continued Existence
Restricted Range and Population Size
The Cumberland darter, rush darter,
yellowcheek darter, chucky madtom,
and laurel dace have limited geographic
ranges and small population sizes. Their
existing populations are extremely
localized, and geographically isolated
from one another, leaving them
vulnerable to localized extinctions from
intentional or accidental toxic chemical
spills, habitat modification, progressive
degradation from runoff (non-point
source pollutants), natural catastrophic
changes to their habitat (e.g., flood
scour, drought), other stochastic
disturbances, and to decreased fitness
from reduced genetic diversity.
Potential sources of unintentional spills
include accidents involving vehicles
transporting chemicals over road
crossings of streams inhabited by one of
these five fish, or the accidental or
intentional release of chemicals used in
agricultural or residential applications
into streams.
Species that are restricted in range
and population size are more likely to
suffer loss of genetic diversity due to
genetic drift, potentially increasing their
susceptibility to inbreeding depression,
decreasing their ability to adapt to
environmental changes, and reducing
the fitness of individuals (Soule 1980,
pp. 157–158; Hunter 2002, pp. 97–101;
Allendorf and Luikart 2007, pp. 117–
146). It is likely that some of the
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Cumberland darter, rush darter,
yellowcheek darter, chucky madtom,
and laurel dace populations are below
the effective population size required to
maintain long-term genetic and
population viability (Soule 1980, pp.
162–164; Hunter 2002, pp. 105–107).
The long-term viability of a species is
founded on the conservation of
numerous local populations throughout
its geographic range (Harris 1984, pp.
93–104). These separate populations are
essential for the species to recover and
adapt to environmental change (Noss
and Cooperrider 1994, pp. 264–297;
Harris 1984, pp. 93–104). The level of
isolation seen in these five species
makes natural repopulation following
localized extirpations virtually
impossible without human intervention.
Climate Change
Climate change has the potential to
increase the vulnerability of the
Cumberland darter, rush darter,
yellowcheek darter, chucky madtom,
and laurel dace to random catastrophic
events (e.g., McLaughlin et al. 2002;
Thomas et al. 2004). Climate change is
expected to result in increased
frequency and duration of droughts and
the strength of storms (e.g., Cook et al.
2004). During 2007, a severe drought
affected the upper Cumberland River
basin in Kentucky and Tennessee.
Streamflow values for the Cumberland
River at Williamsburg, Kentucky (USGS
Station Number 03404000), in
September and October of 2007 were
among the lowest recorded monthly
values (99th percentile for low-flow
periods) during the last 67 years
(Cinotto pers. comm. 2008). Climate
change could intensify or increase the
frequency of drought events, such as the
one that occurred in 2007. Thomas et al.
(2004, p. 112) report that the frequency,
duration, and intensity of droughts are
likely to increase in the Southeast as a
result of global climate change.
Fluker et al. (2007, p. 10) reported
that drought conditions, coupled with
rapid urbanization in watersheds that
contain rush darters, render the
populations vulnerable, especially
during the breeding season when they
concentrate in wetland pools and
shallow pools of headwater streams.
Drought conditions from 2006 to 2007
greatly reduced spawning habitat for
rush darter in Jefferson County
(Drennen pers. obs. 2007). Survey
numbers for the rush darter within the
spring-fed headwaters for the unnamed
tributary to Turkey Creek during 2007
were reduced due to a lack of water
(Kuhajda pers. comm. 2008). In Winston
County, Stiles and Mills (2008, pp. 5–
6) noted that Doe Branch almost
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48739
completely dried up during the summer
of 2007 (Stiles pers. comm. 2008).
The Little Red River watershed in
Arkansas experienced moderate drought
conditions during 1997–2000 (Southern
Regional Climate Center 2000), which
reduced flows in its tributaries and
affected yellowcheek darter
populations. During a status survey for
the species conducted in 2000, the stage
height of the Little Red River was 0.3 m
(1 ft) lower than what was reported
during a 1979–1980 status survey of the
darter (Wine et al. 2000, p. 7). Stream
flow is strongly correlated with
important physical and chemical
parameters that limit the distribution
and abundance of riverine species
(Power et al. 1995, p. 159; Resh et al.
1988, p. 437) and it regulates the
ecological integrity of flowing water
systems (Poff et al. 1997, p. 769). During
the 2000 status survey, the yellowcheek
darter was not found in the upper
reaches of any study streams or in the
Turkey/Beech Fork reach of Devils Fork,
a likely result of drought conditions.
This indicates a contraction of
yellowcheek darter range to stream
reaches lower in the watershed where
flows are maintained for a greater
portion of the year (Wine et al. 2000, p.
11). It is possible that the perceived
contraction in range occurs only during
low precipitation years in north-central
Arkansas. The threat of drought is
imminent and moderate to high,
respectively, in all four watersheds for
the yellowcheek darter. Exacerbation of
natural drought cycles as a result of
global climate change could have
detrimental effects on the species,
which could continue for the
foreseeable future.
Competition From Introduced Species
The Federally endangered watercress
darter (Etheostoma nuchale) was
translocated outside of its native range
by the Service into Tapawingo Springs
in 1988 in order to assist in the species’
recovery by expanding its range (Moss
1995, p. 5). The watercress darter is now
reproducing and is competing with the
rush darter in Tapawingo Springs
(USFWS 1993, p. 1; Drennen pers. obs.
2004; George et al. 2009, p. 532). In
2001, a population of watercress darters
was found in the Penny Springs site
(Stiles and Blanchard 2001, p. 3). The
introduced watercress darter appears to
be out-competing the rush darter at this
site (Fluker et al. 2008, p. 1; George et
al. 2009, p. 532), even though the rush
darter has always been considered rare
in the Tapawingo Spring area (Stiles
pers. comm. 2008). Further investigation
may be required to determine whether
interspecific competition is occurring
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Determination
between the watercress darter and the
rush darter at this site (Stiles pers.
comm. 2008). However, Fluker et al.
(2008, p. 1) and George et al. (2009, p.
532) consider the rush darter to be
extirpated after completing 2 years of
surveys (2008–2009) in Tapawingo
Spring.
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Reduced Fecundity
The low fecundity rates exhibited by
many madtom catfishes (Breder and
Rosen 1966 in Dinkins and Shute 1996,
p. 58) could limit the potential for
populations to rebound from
disturbance events. The short lifespan
exhibited by members of the N.
hildebrandi clade (a taxonomic group of
organisms classified together on the
basis of homologous features traced to a
common ancestor) of madtoms, if also
true of chucky madtoms, would further
limit the species’ viability by rendering
it vulnerable to severe demographic
shifts from disturbances that prevent
reproduction in even a single year, and
could be devastating to the population
if the disturbance persists for successive
years.
Summary
Because the Cumberland darter, rush
darter, yellowcheek darter, chucky
madtom, and laurel dace all have
limited geographic ranges and small
population sizes, they are subject to
several ongoing natural and manmade
threats. Since these threats are ongoing,
they are considered to be imminent. The
magnitude of these threats is high for
each of these species because they result
in a reduced ability to adapt to
environmental change. Further, the
information available to us at this time
does not indicate that the magnitude or
imminence of this threat is likely to be
appreciably reduced in the foreseeable
future.
Exacerbation of natural drought cycles
as a result of global climate change
could have detrimental effects on these
five species, which are expected to
continue or increase in the future. The
specific threat of global climate change
is considered to be nonimminent. The
Federally endangered watercress darter
(Etheostoma nuchale) introduced into
the range of the rush darter is now
potentially competing with the rush
darter. The low fecundity rates
exhibited by many madtom catfishes
could specifically affect the chucky
madtom and exacerbate the problem of
its recovering from disturbance events.
These threats are considered moderate/
low in magnitude because of the
uncertainty of their effects, but are
considered imminent as they are
ongoing.
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We have carefully assessed the best
scientific and commercial information
available regarding the past, present,
and future threats to the Cumberland
darter, rush darter, yellowcheek darter,
chucky madtom, and laurel dace.
Section 3(6) of the Act defines an
endangered species as ‘‘any species
which is in danger of extinction
throughout all or a significant portion of
its range.’’ We find that each of these
five species is presently in danger of
extinction throughout its entire range,
based on the immediacy and magnitude
of the threats described above. Based on
our analysis, we have no reason to
believe that the negative population
trends for any of the five species
addressed in this final rule will
improve, nor will the effects of current
threats acting on the species be
ameliorated in the foreseeable future.
Therefore, on the basis of the best
available scientific and commercial
information, we are listing the
Cumberland darter, rush darter,
yellowcheek darter, chucky madtom,
and laurel dace as endangered under the
Act.
Without the protection of the Act,
these five species are in danger of
extinction throughout all of their highly
localized ranges. Extinction could occur
within a few years, given the reduction
of habitats and ranges, small population
sizes, current habitat threats, and
natural or human-induced catastrophic
events. Furthermore, because of the
immediate and ongoing significant
threats to each species throughout their
entire respective ranges, as described
above in the five-factor analysis, we find
that it is unnecessary to analyze
whether there are any significant
portions of ranges for each species that
may warrant a different determination
of status.
Critical Habitat
In the June 24, 2010 proposed listing
rule (75 FR 36035) we determined that
designation of critical habitat was
prudent for all five species. However,
we found that critical habitat was not
determinable at the time, and set forth
the steps we would undertake to obtain
the information necessary to develop a
proposed designation of critical habitat.
We have completed these steps and
intend to publish a proposed
designation in the next few months for
all five species. We were unable to
include the critical habitat with the final
listing rule due to an internal publishing
issue requiring separate publication of
proposed and final rules in the Federal
Register.
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Available Conservation Measures
Conservation measures provided to
species listed as endangered or
threatened under the Act include
recognition, recovery actions,
requirements for Federal protection, and
prohibitions against certain practices.
Recognition through listing results in
public awareness and conservation
actions by Federal, State, and private
organizations; and individuals. The Act
encourages cooperation with the States
and requires that recovery actions be
carried out for all listed species. The
protection measures required of Federal
agencies and the prohibitions against
certain activities are discussed, in part,
below.
Section 7(a) of the Act requires
Federal agencies to evaluate their
actions with respect to any species that
is proposed or listed as endangered or
threatened and with respect to its
critical habitat, if any is designated.
Regulations implementing this
interagency cooperation provision of the
Act are codified at 50 CFR part 402.
Section 7(a)(4) of the act requires
Federal agencies to confer with the
Service on any action that is likely to
jeopardize the continued existence of a
species proposed for listing or result in
destruction or adverse modification of
proposed critical habitat. If a species is
listed subsequently, section 7(a)(2)
requires Federal agencies to ensure that
activities they authorize, fund, or carry
out are not likely to jeopardize the
continued existence of the species or to
destroy or adversely modify its critical
habitat. If a Federal action may affect a
listed species or its critical habitat, the
responsible Federal agency must enter
into formal consultation with the
Service.
Federal agency actions within the
species’ habitat that may require
conference or consultation or both as
described in the preceding paragraph
include, but are not limited to, the
carrying out or the issuance of permits
for reservoir construction, stream
alterations, discharges, wastewater
facility development, water withdrawal
projects, pesticide registration, mining,
and road and bridge construction.
The Act and its implementing
regulations set forth a series of general
prohibitions and exceptions that apply
to all endangered wildlife. The
prohibitions, codified at 50 CFR 17.21
for endangered wildlife, in part, make it
illegal for any person subject to the
jurisdiction of the United States to take
(includes harass, harm, pursue, hunt,
shoot, wound, kill, trap, capture, or
collect, or to attempt any of these),
import or export, ship in interstate
E:\FR\FM\09AUR1.SGM
09AUR1
48741
Federal Register / Vol. 76, No. 153 / Tuesday, August 9, 2011 / Rules and Regulations
commerce in the course of commercial
activity, or sell or offer for sale in
interstate or foreign commerce any
listed species. It also is illegal to
possess, sell, deliver, carry, transport, or
ship any wildlife that has been taken
illegally. Certain exceptions apply to
agents of the Service and State
conservation agencies.
We may issue permits to carry out
otherwise prohibited activities
involving endangered wildlife species
under certain circumstances.
Regulations governing permits are
codified at 50 CFR 17.22 for endangered
species, and at 17.32 for threatened
species. With regard to endangered
wildlife, a permit must be issued for the
following purposes: for scientific
purposes, to enhance the propagation or
survival of the species, and for
incidental take in connection with
otherwise lawful activities.
governments, individuals, businesses, or
organizations. An agency may not
conduct or sponsor, and a person is not
required to respond to, a collection of
information unless it displays a
currently valid OMB control number.
Required Determinations
A complete list of all references cited
in this rulemaking is available on the
Internet at https://www.regulations.gov
or upon request from the Field
Supervisor, Tennessee Ecological
Services Field Office (see FOR FURTHER
INFORMATION CONTACT).
Paperwork Reduction Act of 1995 (44
U.S.C. 3501 et seq.)
This rule does not contain any new
collections of information that require
approval by the Office of Management
and Budget (OMB) under the Paperwork
Reduction Act. This rule will not
impose recordkeeping or reporting
requirements on State or local
National Environmental Policy Act
(NEPA)
We have determined that
environmental assessments and
environmental impact statements, as
defined under the authority of the
National Environmental Policy Act of
1969 (42 U.S.C. 4321 et seq.), need not
be prepared in connection with
regulations pursuant to section 4(a) of
the Act. We published a notice outlining
our reasons for this determination in the
Federal Register on October 25, 1983
(48 FR 49244).
References Cited
The primary authors of this document
are the staff members of the Tennessee
Vertebrate population where endangered or threatened
Historic range
Common name
Scientific name
*
FISHES
*
List of Subjects in 50 CFR Part 17
Endangered and threatened species,
Exports, Imports, Reporting and
recordkeeping requirements,
Transportation.
Regulation Promulgation
Accordingly, we amend part 17,
subchapter B of chapter I, title 50 of the
Code of Federal Regulations, as follows:
PART 17—[AMENDED]
1. The authority citation for part 17
continues to read as follows:
■
Authority: 16 U.S.C. 1361–1407; 16 U.S.C.
1531–1544; 16 U.S.C. 4201–4245; Pub. L. 99–
625, 100 Stat. 3500; unless otherwise noted.
2. Amend § 17.11(h) by adding entries
for ‘‘Dace, laurel,’’ ‘‘Darter,
Cumberland,’’ ‘‘Darter, rush,’’ ‘‘Darter,
yellowcheek,’’ and ‘‘Madtom, chucky’’
to the List of Endangered and
Threatened Wildlife, in alphabetical
order, under FISHES, to read as follows:
■
Authors
Species
Ecological Services Field Office (see FOR
FURTHER INFORMATION CONTACT).
*
*
§ 17.11 Endangered and threatened
wildlife.
*
Status
*
*
(h) * * *
*
When listed
*
*
Critical habitat
*
*
*
Dace, laurel .............
*
Chrosomus saylori ..
*
U.S.A (TN) ..............
*
Entire ......................
*
E
*
791
NA
*
Darter, Cumberland
*
Etheostoma
susanae.
*
U.S.A. (KY, TN) ......
*
Entire ......................
*
E
*
791
NA
*
Darter, rush ..............
*
Etheostoma
phytophilum.
*
U.S.A. (AL) .............
*
Entire ......................
*
E
*
791
NA
*
Darter, yellowcheek
*
Etheostoma moorei
*
U.S.A. (AR) .............
*
Entire ......................
*
E
*
791
NA
*
Madtom, chucky ......
*
Noturus crypticus ....
*
U.S.A. (TN) .............
*
Entire ......................
*
E
*
791
NA
*
*
*
*
jlentini on DSK4TPTVN1PROD with RULES
Special
rules
*
*
*
*
*
*
Dated: July 27, 2011.
James J. Slack,
Acting Director, U.S. Fish and Wildlife
Service.
*
[FR Doc. 2011–20018] Filed 8–8–11; 8:45 am]
BILLING CODE 4310–55–P
VerDate Mar<15>2010
16:10 Aug 08, 2011
Jkt 223001
PO 00000
Frm 00029
Fmt 4700
Sfmt 9990
E:\FR\FM\09AUR1.SGM
09AUR1
*
NA
*
NA
*
NA
*
NA
*
NA
*
Agencies
[Federal Register Volume 76, Number 153 (Tuesday, August 9, 2011)]
[Rules and Regulations]
[Pages 48722-48741]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2011-20018]
=======================================================================
-----------------------------------------------------------------------
DEPARTMENT OF THE INTERIOR
Fish and Wildlife Service
50 CFR Part 17
[Docket No. FWS-R4-ES-2011-0027; MO 92210-0-0008 B2]
RIN 1018-AV85
Endangered and Threatened Wildlife and Plants; Endangered Status
for the Cumberland Darter, Rush Darter, Yellowcheek Darter, Chucky
Madtom, and Laurel Dace
AGENCY: Fish and Wildlife Service, Interior.
ACTION: Final rule.
-----------------------------------------------------------------------
SUMMARY: We, the U.S. Fish and Wildlife Service (Service), determine
endangered status for the Cumberland darter (Etheostoma susanae), rush
darter (Etheostoma phytophilum), yellowcheek darter (Etheostoma
moorei), chucky madtom (Noturus crypticus), and laurel dace (Chrosomus
saylori) under the Endangered Species Act of 1973, as amended (Act).
This final rule implements the Federal protections provided by the Act
for these species throughout their ranges, including Cumberland darter
in Kentucky and Tennessee, rush darter in Alabama, yellowcheek darter
in Arkansas, and chucky madtom and laurel dace in Tennessee. We intend
to propose critical habitat in an upcoming rulemaking, which is
expected within the next few months.
DATES: This rule becomes effective September 8, 2011.
ADDRESSES: This final rule is available on the Internet at https://www.regulations.gov at Docket No. FWS-R4-ES-2010-0027. Comments and
materials received, as well as supporting documentation used in the
preparation of this rule, will be
[[Page 48723]]
available for public inspection, by appointment, during normal business
hours at: U.S. Fish and Wildlife Service, Tennessee Ecological Services
Field Office, 446 Neal Street, Cookeville, TN 38501; telephone 931-528-
6481; facsimile 931-528-7075.
FOR FURTHER INFORMATION CONTACT: For information regarding the
Cumberland darter, contact Lee Andrews, Field Supervisor, U.S. Fish and
Wildlife Service, Kentucky Ecological Services Field Office, J.C. Watts
Federal Building, 330 W. Broadway Rm. 265, Frankfort, KY 40601;
telephone 502-695-0468; facsimile 502-695-1024.
For information regarding the rush darter, contact Stephen Ricks,
Field Supervisor, U.S. Fish and Wildlife Service, Mississippi
Ecological Services Field Office, 6578 Dogwood View Parkway, Suite A,
Jackson, MS 39213; telephone 601-965-4900; facsimile 601-965-4340 or
Bill Pearson, Field Supervisor, U.S. Fish and Wildlife Service, Alabama
Ecological Services Field Office, 1208-B Main Street, Daphne, AL 36526;
telephone 251-441-5181; fax 251-441-6222.
For information regarding the yellowcheek darter, contact Jim
Boggs, Field Supervisor, U.S. Fish and Wildlife Service, Arkansas
Ecological Services Field Office, 110 South Amity Road, Suite 300,
Conway, AR 72032; telephone 501-513-4470; facsimile 501-513-4480.
For information regarding the chucky madtom and laurel dace,
contact Mary Jennings, Field Supervisor, U.S. Fish and Wildlife
Service, Tennessee Ecological Services Field Office, 446 Neal Street,
Cookeville, TN 38501; telephone 931-528-6481; facsimile 931-528-7075.
If you use a telecommunications device for the deaf (TDD), call the
Federal Information Relay Service (FIRS) at 800-877-8339.
SUPPLEMENTARY INFORMATION:
Background
This document consists of a final rule to list the Cumberland
darter (Etheostoma susanae), rush darter (Etheostoma phytophilum),
yellowcheek darter (Etheostoma moorei), chucky madtom (Noturus
crypticus), and laurel dace (Chrosomus saylori) as endangered under the
Endangered Species Act of 1973, as amended (16 U.S.C. 1531 et seq.)
(Act). The Act requires that we identify species of wildlife and plants
that are endangered or threatened, based on the best available
scientific and commercial information. As defined in section 3 of the
Act, an endangered species is any species which is in danger of
extinction throughout all or a significant portion of its range, and a
threatened species is any species which is likely to become an
endangered species within the foreseeable future throughout all or a
significant portion of its range.
Through the Federal rulemaking process, we add species that meet
these definitions to the List of Endangered and Threatened Wildlife at
50 CFR 17.11 or the List of Endangered and Threatened Plants at 50 CFR
17.12. As part of this program, we maintain a list of species that we
regard as candidates for listing. We call this list the Candidate
Notice of Review (CNOR). A candidate species is one for which we have
on file sufficient information on biological vulnerability and threats
to support a proposal to list as endangered or threatened, but for
which preparation and publication of a proposal is precluded by higher
priority listing actions. We may identify a species as a candidate for
listing based on an evaluation of its status that we conducted on our
own initiative, or as a result of making a finding on a petition to
list a species that listing is warranted but precluded by other higher
priority listing action. Table 1 includes the citation information for
the CNORs mentioned in the following paragraphs, which discuss the
previous candidate status of each of the five species being listed as
endangered in this rule.
Table 1--Federal Register Citation Information for Certain Candidate Notices of Review Issued by the U.S. Fish
and Wildlife Service Since 1985
----------------------------------------------------------------------------------------------------------------
Federal Register volume and Date of publication in the Federal
Year page number Register
----------------------------------------------------------------------------------------------------------------
1985..................................... 50 FR 37958................. September 18, 1985.
1989..................................... 54 FR 554................... January 6, 1989.
1991..................................... 56 FR 58804................. November 21, 1991.
1994..................................... 59 FR 58982................. November 15, 1994.
1996..................................... 61 FR 7596.................. February 28, 1996.
1999..................................... 64 FR 57533................. October 25, 1999.
2001..................................... 66 FR 54807................. October 30, 2001.
2002..................................... 67 FR 40657................. June 13, 2002.
2004..................................... 69 FR 24875................. May 4, 2004.
2005..................................... 70 FR 24869................. May 11, 2005.
2006..................................... 71 FR 53755................. September 12, 2006.
2007..................................... 72 FR 69034................. December 6, 2007.
2008..................................... 73 FR 75176................. December 10, 2008.
2009..................................... 74 FR 57804................. November 9, 2009.
2010..................................... 75 FR 69222................. November 10, 2010.
----------------------------------------------------------------------------------------------------------------
Previous Federal Action
Cumberland Darter
The Cumberland darter was first identified as a candidate for
listing in the 1985 CNOR. It was assigned a Category 2 status, which
was given to those species for which the Service possessed information
indicating that proposing to list as endangered or threatened was
possibly appropriate, but for which conclusive data on biological
vulnerability and threat was not currently available to support
proposed rules. The Cumberland darter retained the Category 2 status in
the 1989, 1991, and 1994 CNORs.
Assigning categories to candidate species was discontinued in 1996,
and only species for which the Service had sufficient information on
biological vulnerability and threats to support issuance of a proposed
rule were regarded as candidate species. Candidate species were also
assigned listing priority numbers based on immediacy and the magnitude
of threat, as well as their taxonomic status. In the 1999, 2001, 2002,
and 2004 CNORs, the Cumberland darter was identified as a
[[Page 48724]]
listing priority 6 candidate species. We published a petition finding
for Cumberland darter in the 2005 CNOR in response to a petition
received on May 11, 2004, stating the darter would retain a listing
priority of 6.
In the 2006 CNOR, we changed the listing priority number for
Cumberland darter from 6 to 5, because it was formally described as a
distinct species. Based on new molecular evidence, the subspecies
Etheostoma nigrum susanae was elevated to specific status, Etheostoma
susanae. In the 2007, 2008, 2009, and 2010 CNORs, the Cumberland darter
retained a listing priority of 5. On June 24, 2010 (75 FR 36035) we
published a proposed rule to list the Cumberland darter as endangered.
Rush Darter
We first identified the rush darter as a candidate for listing in
the 2002 CNOR. The rush darter was assigned a listing priority number
of 5. In the 2004 CNOR, the rush darter retained a listing priority
number of 5. We published a petition finding for rush darter in the
2005 CNOR in response to a petition received on May 11, 2004, stating
the darter would retain a listing priority of 5.
In 2006, we changed the listing priority number of the rush darter
from 5 to 2 based on the imminent threat of water quality deterioration
(i.e., increased sedimentation due to urbanization, road maintenance,
and silviculture practices). In the 2007, 2008, 2009, and 2010 CNORs,
the rush darter retained a listing priority of 2. We proposed to list
the rush darter as endangered on June 24, 2010 (75 FR 36035).
Yellowcheek Darter
We first identified the yellowcheek darter as a candidate for
listing in the 2001 CNOR with a listing priority of 2. The yellowcheek
darter retained a listing priority number of 2 in the 2002 and 2004
CNORs. We published a petition finding for yellowcheek darter in the
2005 CNOR in response to a petition received on May 11, 2004, stating
the darter would retain a listing priority of 2.
In the 2006, 2007, 2008, 2009, and 2010 CNORs, the yellowcheek
darter retained a listing priority of 2. The yellowcheek darter is
covered by a 2007 programmatic Candidate Conservation Agreement with
Assurances (71 FR 53129) that covers the entire range of the species.
We proposed to list the yellowcheek darter as endangered on June 24,
2010 (75 FR 36035).
Chucky Madtom
We first identified the chucky madtom as a candidate for listing in
the 1994 CNOR with a Category 2 status. In the 2002 and 2004 CNORs, the
chucky madtom was identified as a listing priority 2 candidate species.
We published a petition finding for chucky madtom in the 2005 CNOR in
response to a petition received on May 11, 2004, stating the madtom
would retain a listing priority of 2. In the 2006, 2007, 2008, 2009,
and 2010 CNORs, the chucky madtom retained a listing priority of 2.
In 1994, the chucky madtom was first added to the candidate list as
Noturus sp. Subsequently, and based on morphological and molecular
evidence, the chucky madtom was formally described as a distinct
species, Noturus crypticus (Burr et al. 2005). We included this new
information in the 2006 CNOR. We proposed to list the chucky madtom as
endangered on June 24, 2010 (75 FR 36035).
Laurel Dace
We first identified the laurel dace as a new candidate for listing
in the 2007 CNOR. New candidates are those taxa for which we have
sufficient information on biological vulnerability and threats to
support preparation of a listing proposal, but for which development of
a listing regulation is precluded by other higher priority listing
activities.
In the 2007 CNOR, we assigned the laurel dace a listing priority of
5. The laurel dace retained a listing priority of 5 in the 2008, 2009,
and 2010 CNORs. We proposed to list the laurel dace as endangered on
June 24, 2010 (75 FR 36035).
Species Information
Cumberland Darter
The Cumberland darter (Etheostoma (Boleosoma) susanae (Jordan and
Swain)) is a medium-sized member of the fish tribe Etheostomatini
(family Percidae) that reaches over 5.5 centimeters (cm) (2 inches
(in)) standard length (SL) (length from tip of snout to start of the
caudal peduncle (slender region extending from behind the anal fin to
the base of the caudal fin)) (Etnier and Starnes 1993, p. 512). The
species has a straw-yellow background body color with brown markings
that form six evenly spaced dorsal (back) saddles and a series of X-,
C-, or W-shaped markings on its sides (Etnier and Starnes 1993, p.
510). During spawning season, the overall body color of breeding males
darkens, and the side markings become obscure or appear as a series of
blotches (Etnier and Starnes 1993, p. 510).
The Cumberland darter was first described as Boleosoma susanae by
Jordan and Swain (1883, pp. 249-250) from tributaries of the Clear Fork
of the Cumberland River, Kentucky. Subsequent studies by Kuhne (1939,
p. 92) and Cole (1967, p. 29) formerly recognized the taxon as a
subspecies (Etheostoma nigrum susanae) of E. n. nigrum (Johnny darter).
Starnes and Starnes (1979, p. 427) clarified the subspecific status of
the Cumberland darter, differentiating it from the Johnny darter by
several diagnostic characteristics. Strange (1998, p. 101) elevated E.
n. susanae to full species status based on analyses of mitochondrial
DNA for E. n. susanae and E. n. nigrum.
The Cumberland darter inhabits pools or shallow runs of low- to
moderate-gradient sections of streams with stable sand, silt, or sand-
covered bedrock substrates (O'Bara 1988, pp. 10-11; O'Bara 1991, p. 10;
Thomas 2007, p. 4). Thomas (2007, p. 4) did not encounter the species
in high-gradient sections of streams or areas dominated by cobble or
boulder substrates. Thomas (2007, p. 4) reported that streams inhabited
by Cumberland darters were second to fourth order, with widths ranging
from 4 to 9 meters (m) (11 to 30 feet (ft)) and depths ranging from 20
to 76 cm (8 to 30 in).
Little is known regarding the reproductive habits of the Cumberland
darter. Thomas (2007, p. 4) reported the collection of males in
breeding condition in April and May, with water temperatures ranging
from 15 to 18 degrees Celsius ([deg]C) (59 to 64 degrees Fahrenheit
([deg]F)). Extensive searches by Thomas (2007, p. 4) produced no
evidence of nests or eggs at these sites. Species commonly associated
with the Cumberland darter during surveys by Thomas (2007, pp. 4-5)
were creek chub (Semotilus atromaculatus), northern hogsucker
(Hypentelium nigricans), stripetail darter (E. kennicotti), and
Cumberland arrow darter (E. sagitta sagitta). Feeding habits are
unknown but are likely similar to that of the closely related species,
the Johnny darter (E. nigrum). Johnny darters are sight feeders, with
prey items consisting of midge larvae, mayfly nymphs, caddisfly larvae,
and microcrustaceans (Etnier and Starnes 1993, p. 511). Thomas (2007,
p. 5) collected individuals of the Federally threatened blackside dace
(Chrosomus cumberlandensis), from three streams that also supported
Cumberland darters.
The Cumberland darter is endemic to the upper Cumberland River
system
[[Page 48725]]
above Cumberland Falls in Kentucky and Tennessee (O'Bara 1988, p. 1;
O'Bara 1991, p. 9; Etnier and Starnes 1993, p. 511). The earliest known
collections of the species were made by Jordan and Swain (1883, pp.
249-250), who recorded it as abundant in tributaries of Clear Fork of
the Cumberland River, Kentucky. The species was later reported from Gum
Fork, Scott County, Tennessee, by Shoup and Peyton (1940, p. 11), and
seven additional tributaries of the Cumberland River by Burr and Warren
(1986, p. 310). More exhaustive surveys by O'Bara (1988, p. 6; 1991,
pp. 9-10) and Laudermilk and Cicerello (1998; pp. 83-233, 303-408)
determined that the Cumberland darter was restricted to short reaches
of 20 small streams (23 sites) in the upper Cumberland River system in
Whitley and McCreary Counties, Kentucky, and Campbell and Scott
Counties, Tennessee. These studies suggested the extirpation of the
species from Little Wolf Creek in Whitley County, Kentucky, and Gum
Fork in Scott County, Tennessee. Preliminary reports of disjunct
populations in the Poor Fork Cumberland River and Martins Fork in
Letcher and Harlan Counties, Kentucky (Starnes and Starnes 1979, p.
427; O'Bara 1988, p. 6; O'Bara 1991, pp. 9-10), were evaluated
genetically and determined to be the Johnny darter (Strange 1998, p.
101).
Thomas (2007, p. 3) provided the most recent information on status
and distribution of the species through completion of a range-wide
status assessment in the upper Cumberland River drainage in Kentucky.
Between June 2005 and April 2007, a total of 47 sites were sampled
qualitatively in the upper Cumberland River drainage. All Kentucky
sites with historic records were surveyed (20 sites), as well as 27
others having potentially suitable habitat. Surveys by Thomas (2007, p.
3) produced a total of 51 specimens from 13 localities (12 streams).
Only one of the localities represented a new occurrence record for the
species.
In 2008, the Kentucky Department of Fish and Wildlife Resources
(KDFWR) initiated a propagation and reintroduction project for the
Cumberland darter in the upper Cumberland River drainage (Thomas et al.
2010, p. 107). Utilizing State Wildlife Grant funds from the Service,
KDFWR worked cooperatively with Conservation Fisheries, Inc. (CFI) of
Knoxville, Tennessee, to develop captive propagation protocols for the
species and to produce juvenile Cumberland darters that could be
reintroduced within the species' historic range. Cogur Fork, a
tributary to Indian Creek in McCreary County, Kentucky, was chosen by
KDFWR as a suitable reintroduction site. Cumberland darters were
released into Cogur Fork in August 2009 and September 2010. Surveys in
November 2010 resulted in recaptures of individuals released in 2009
and 2010, as well as captures of four individuals without tags
(possibly native individuals) (Thomas pers. comm. 2010). Based on these
results, it appears that reintroduction efforts have been effective,
with Cumberland darters persisting within Cogur Fork since 2009.
Furthermore, captures of untagged individuals in 2009 and 2010 suggest
that Cogur Fork also supports a small, native population of the
species.
Currently, the Cumberland darter is known from 15 localities in a
total of 13 streams in Kentucky (McCreary and Whitley Counties) and
Tennessee (Campbell and Scott Counties). All 15 extant occurrences of
the Cumberland darter are restricted to short stream reaches, with the
majority believed to be restricted to less than 1.6 kilometers (km) (1
mile (mi)) of stream (O'Bara 1991, pp. 9-10; Thomas 2007, p. 3). These
occurrences are thought to form six population clusters (Bunches Creek,
Indian Creek, Marsh Creek, Jellico Creek, Clear Fork, and Youngs
Creek), which are geographically separated from one another by an
average distance of 30.5 stream km (19 stream mi) (O'Bara 1988, p. 12;
O'Bara 1991, p. 10; Thomas 2007, p. 3). Based on collection efforts by
O'Bara (1991, pp. 9-10), Laudermilk and Cicerello (1998; pp. 83-233,
303-408), and Thomas (2007, p. 3), the species appears to be extirpated
from 11 historical collection sites and a total of 9 streams:
Cumberland River mainstem, near the mouth of Bunches Creek and
Cumberland Falls (Whitley County); Sanders Creek (Whitley County);
Brier Creek (Whitley County); Kilburn Fork of Indian Creek (McCreary
County); Bridge Fork (McCreary County); Marsh Creek, near mouth of Big
Branch and Caddell Branch (McCreary County); Cal Creek (McCreary
County); Little Wolf Creek (Whitley County); and Gum Fork (Scott
County). No population estimates or status trends are available for the
Cumberland darter; however, survey results by Thomas (2007, p. 3)
suggest that the species is uncommon or occurs in low densities across
its range (Thomas 2007, p. 3).
The Cumberland darter is ranked by the Kentucky State Nature
Preserves Commission (KSNPC) (2009, p. 38) and the Tennessee Department
of Environment and Conservation (TDEC) (2009, p. 53) as a G1G2S1
species: critically imperiled or imperiled globally and critically
imperiled in Kentucky and Tennessee. The KDFWR State Wildlife Action
Plan identified the Cumberland darter as a species of Greatest
Conservation Need (GCN) and identified several top conservation actions
for it and other species in its Aquatic Guild (Upland Headwater Streams
in Pools), including: Acquisition or conservation easements for
critical habitat, development of financial incentives to protect
riparian (land adjacent to stream channel) corridors, development and
implementation of best management practices, and restoration of
degraded habitats through various State and Federal programs (KDFWR
2005, p. 2.2.2). The Cumberland darter is designated as a Tier 1 GCN
species in the Tennessee Comprehensive Wildlife Conservation Strategy
(CWCS) (TWRA 2005, pp. 44, 49).
Rush Darter
The rush darter (Etheostoma phytophilum) is a medium-sized darter
in the family Percidae, tribe Etheostomatini, and subgenus Fuscatelum.
The species reaches an average size of 5 cm (2 in) SL (Bart and Taylor
1999, p. 28; Johnston and Kleiner 2001, p. 3). The rush darter was
described by Bart and Taylor in 1999 (pp. 27-33), and is closely
related to the goldstripe darter (E. parvipinne), a drab-colored
species with a thin golden stripe along the lateral line (canal along
the side of a fish with sensory capabilities) that is surrounded by
heavily mottled or stippled sides (Shaw 1996, p. 85). However, the
distinct golden stripe characteristic of goldstripe darters is not well
developed in rush darters (Bart and Taylor 1999, p. 29). Also, the
brown pigment on the sides of the rush darter is usually not as intense
as in the goldstripe darter. Other characteristics of the rush darter
are described in Bart and Taylor (1999, p. 28).
Rush darters have been collected from various habitats (Stiles and
Mills 2008, pp. 1-4; Bart 2002, p. 1; Johnston and Kleiner 2001, pp. 3-
4; Stiles and Blanchard 2001, pp. 1-4; Bart and Taylor 1999, p. 32),
including root masses of emergent vegetation along the margins of
spring-fed streams in very shallow, clear, cool, and flowing water; and
from both small clumps and dense stands of bur reed (Sparganium sp.),
coontail (Ceratophyllum sp.), watercress (Nasturtium officinale), and
rush (Juncus sp.) in streams with substrates of silt, sand, sand and
silt, muck and sand or some gravel with sand, and bedrock. Rush darters
appear to prefer springs and spring-fed reaches of relatively low-
gradient small streams,
[[Page 48726]]
which are generally influenced by springs (Stiles and Mills 2008, pp.
1-4; Fluker et al. 2007, p. 1; Bart 2002, p. 1; Johnston and Kleiner
2001, pp. 3-4; Stiles and Blanchard 2001, pp. 1-4; Bart and Taylor
1999, p. 32). Rush darters have also been collected in wetland pools
(Stiles and Mills 2008; pp. 2-3). Water depth at collection sites
ranged from 3.0 cm to 0.5 m (0.1 ft to 1.6 ft), with moderate water
velocity in riffles and no flow or low flow in pools. Rush darters have
not been found in higher gradient streams with bedrock substrates and
sparse vegetation (Stiles and Mills 2008, pp. 1-4; Bart 2002, p. 1;
Johnston and Kleiner 2001, pp. 3-4; Stiles and Blanchard 2001, pp. 1-4;
Bart and Taylor 1999, p. 32).
Stiles and Mills (2008, p. 2) found gravid rush darter females in
February and fry (newly hatched larval fish) in late April from a
wetland pool in the Mill Creek watershed (Winston County, Alabama).
These pools act as nursery areas for the fry (Stiles and Mills 2008, p.
5). While little is known specifically about the life history of the
rush darter, this information is available for the goldstripe darter, a
related species in the Etheostoma genus. Spawning of the goldstripe
darter in Alabama occurs from mid-March through June (Mettee et al.
1996, p. 655). Preferred food items for the goldstripe darter include
midge larvae, mayfly nymphs, blackfly larvae, beetles, and
microcrustaceans (Mettee et al. 1996, p. 655). The lifespan of the
goldstripe darter is estimated to be 2 to 3 years.
The rush darter currently has a restricted distribution (Johnston
and Kleiner 2001, p. 1). All rush darter populations are located above
the Fall Line (the inland boundary of the Coastal Plain physiographic
region) and in other ``highland regions'' where topography and
elevation changes are observed presenting a barrier for fish movement
(Boshung and Mayden 2004, p. 18) in the Black Warrior River drainage in
portions of the Appalachian Plateau and Valley and Ridge physiographic
provinces of Alabama (Boshung and Mayden 2004, pp. 16-17; Warren et al.
2000, pp. 9, 10, 24). The closely related goldstripe darter in Alabama
occurs essentially below the Fall Line in all major systems except the
Coosa system (Boshung and Mayden 2004, p. 550). Reports of goldstripe
darters from the 1960s and 1970s in Winston and Jefferson Counties,
Alabama (Caldwell 1965, pp. 13-14; Barclay 1971, p. 38; Dycus and
Howell 1974, pp. 21-24; Mettee et al. 1989, pp. 13, 61, 64), which are
above the Fall Line, were made prior to the description of the rush
darter, but are now considered to be rush darters (Kuhajda pers. comm.
2008).
Historically, rush darters have been found in three distinct
watersheds in Alabama: Doe Branch, Wildcat Branch, and Mill Creek of
the Clear Creek drainage in Winston County; an unnamed spring run of
Beaver Creek and Penny Springs of the Turkey Creek drainage in
Jefferson County; and Cove Spring (Little Cove Creek system) and
Bristow Creek of the Locust Fork drainage in Etowah County. Fluker et
al. (2007, p. 10) suggests that the unique topographic and geologic
influences in the three distinct population groups likely produced
different selective pressures, genetic isolation, genetic drift, and
divergence during the species' evolution.
Currently, the three rush darter populations occur in the same
watersheds but in a more limited distribution. One population is
located in Wildcat Branch and Mill Creek in the Clear Creek drainage in
Winston County (Johnston and Kleiner 2001, p. 4; Stiles and Mills 2008,
pp. 1-3); the second is located in an unnamed spring run to Beaver
Creek, portions of Beaver Creek, and an unnamed tributary to Turkey
Creek in the Turkey Creek drainage in Jefferson County (Stiles and
Blanchard 2001, p. 2; Drennen pers. obsv. 2006-2010; Kuhajda pers.
comm. 2009); and the third is in the Little Cove Creek drainage (Bart
and Taylor 1999, p. 28; Bart 2002, p. 7; Kuhajda pers. comm. 2008-2009;
Spadgenski pers. comm. 2008-2009).
Rush darter populations are separated from each other
geographically, and individual rush darters are only sporadically
collected at a particular site within their range. Where it occurs, the
rush darter is apparently an uncommon species that is usually collected
in low numbers (compiled from Bart and Taylor 1999, pp. 31-32; Johnston
and Kleiner 2001, pp. 2-4; Stiles and Blanchard 2001, pp. 1-4; Johnston
2003, pp. 1-3; Stiles and Mills 2008, pp. 1-3; Rakes pers. comm. 2010;
Drennen pers. obsv. 2006-2010; Kuhajda pers. comm. 2009); however,
there are no population estimates at this time.
Cumulatively, the rush darter is only known from localized
collection sites within approximately 14.5 km (9 mi) of streams in the
Clear Creek; Little Cove and Bristow Creek; and Turkey Creek drainages
in Winston, Etowah, and Jefferson Counties, respectively. Currently,
about 3 km (2 mi) of stream, or about 22 percent of the rush darter's
known range, is not occupied.
Within the Clear Creek drainage, the rush darter has been collected
in Wildcat Branch, Mill Creek, and Doe Creek, which represents about 13
km (9 mi) of stream or about 89 percent of the species' total
cumulative range. Recent surveys (Stiles and Mills 2008, pp. 1-4;
Johnston and Kleiner 2001, p. 3) have failed to document the absence of
the rush darter in Doe Creek, indicating a potential reduction of the
species' known range within the Clear Creek drainage by about 3 km (2
mi) of stream or 22 percent. However, rush darters were collected in
2005, 2008, and 2009 in the Little Cove Creek drainage (Cove Spring
run), after a 30 year period of not finding the species. This
rediscovery of the species confirms the continued existence of the
species in Etowah County and Cove Spring. However, the Little Cove
Creek drainage constitutes an increase of only 0.05 km (0.02 mi) of
occupied stream habitat or a 0.22 percent addition to the total range
of the species. No collections of the species have occurred at Bristow
Creek since 1997. Bristow Creek has since been channelized
(straightened and deepened to increase water velocity). In the Turkey
Creek drainage, rush darters have been collected sporadically within
Penny Springs and at the type locality for the species (an unnamed
spring run in Jefferson County, Alabama) (Bart and Taylor 1999, pp. 28,
33). However, the rush darter is likely extirpated from Penny and
Tapawingo Springs due to introductions of the watercress darter (E.
nuchale) (George et al. 2009, p. 532). The species can still be found
in portions of an unnamed tributary of Beaver Creek and an unnamed
spring to Beaver Creek (Kuhajda pers. comm. 2009). This area contains
about 1.6 km (1 mi) of occupied stream habitat or approximately 11
percent of the rush darter's total range.
The rush darter is ranked by the Alabama Department of Conservation
and Natural Resources (ADCNR) (Wildlife and Freshwater Fisheries
Division, ADCNR 2005) as a P1G1S1 species signifying its rarity in
Alabama and its status as critically imperiled globally. It is also
considered a species of GCN by the State (Bart 2004, p. 193). The rush
darter has a High Priority Conservation Actions Needed and Key
Partnership Opportunities ranking of ``CA 6,'' the highest of any fish
species listed. The State Wildlife Action Plan states that the species
consists of disjoint populations and information is needed to determine
genetic structuring within the populations (Wildlife and Freshwater
Fisheries Division, ADCNR 2005). Conservation Actions for the species
may require population augmentation or reintroduction of the
[[Page 48727]]
species to suitable habitats to maintain viability.
Yellowcheek Darter
The yellowcheek darter (Etheostoma moorei) is a small and
laterally-compressed fish that attains a maximum SL of about 6.4 cm
(2.5 in), and has a moderately sharp snout, deep body, and deep caudal
peduncle (Raney and Suttkus 1964, p. 130). The back and sides are
grayish brown, often with darker brown saddles and lateral bars.
Breeding males are brightly colored with a bright blue or brilliant
turquoise throat and breast and a light-green belly, while breeding
females possess orange and red-orange spots but are not brightly
colored (Robison and Buchanan 1988, pp. 427-429).
First collected in 1959 from the Devils Fork Little Red River,
Cleburne County, Arkansas, this species was eventually described by
Raney and Suttkus in 1964, using 228 specimens from the Middle, South,
and Devils Forks of the Little Red River (Devils Fork, Turkey Fork, and
Beech Fork represent one stream with three different names and are
subsequently referred to in this rule as ``Devils Fork''). Wood (1996,
p. 305) verified the taxonomic status of the yellowcheek darter within
the subgenus Nothonotus. Complete taxonomy for the species is family
Percidae, subfamily Percinae, tribe Etheostomatini, genus Etheostoma,
subgenus Nothonotus and E. tippecanoe species group (Wood 1996, p.
307). The yellowcheek darter is one of only two members of the subgenus
Nothonotus known to occur west of the Mississippi River.
The yellowcheek darter inhabits high-gradient headwater tributaries
with clear water; permanent flow; moderate to strong riffles; and
gravel, rubble, and boulder substrates (Robison and Buchanan 1988, p.
429). Yellowcheek darter prey items include aquatic fly larvae,
stonefly larvae, mayfly nymphs, and caddisfly larvae (McDaniel 1984, p.
56).
Male and female yellowcheek darters reach sexual maturity at 1 year
of age, and maximum lifespan is around 5 years (McDaniel 1984, pp. 25,
76). Spawning occurs from late May through June in the swift to
moderately swift portions of riffles, often around or under the largest
substrate particles (McDaniel 1984, p. 82), although brooding females
have been found at the head of riffles in smaller gravel substrate
(Wine et al. 2000, p. 3). During nonspawning months, there is a general
movement to portions of the riffle with smaller substrate, such as
gravel or cobble, and less turbulence (Robison and Harp 1981, p. 3).
Weston and Johnson (2005, p. 24) observed that the yellowcheek darter
moved very little during a 1-year migration study. It was noted that
the yellowcheek darter appears to be a relatively nonmobile species,
with 19 of 22 recaptured darters found within 9 m (29.5 ft) of their
original capture position after periods of several months. A number of
life-history characteristics including courtship patterns, specific
spawning behaviors, egg deposition sites, number of eggs per nest,
degree of nest protection by males, and degree of territoriality are
unknown at this time; however, researchers have suggested that the
yellowcheek darter deposits eggs on the undersides of large rubble in
swift water (McDaniel 1984, p. 82). Wine and Blumenshine (2002, p. 10)
noted that, during laboratory spawning, female yellowcheek darters bury
themselves in fine gravel or sand substrates (often behind large cobble
or boulders) with only their heads and caudal fin exposed. A male
yellowcheek darter will then position upstream of the buried female and
fertilize her eggs as she releases them in a vibrating motion. Clutch
size and nest defense behavior were not observed.
The yellowcheek darter is endemic to the Devils, Middle, South, and
Archey Forks of the Little Red River and mainstem Little Red River in
Cleburne, Searcy, Stone, and Van Buren Counties, Arkansas (Robison and
Buchanan 1988, p. 429). In 1962, the construction of a dam on the
Little Red River to create Greers Ferry Reservoir impounded much of the
range of this species, including the lower reaches of Devils Fork,
Middle Fork, South Fork, and portions of the mainstem Little Red River,
thus extirpating the species from these reaches. Yellowcheek darter was
also extirpated from the Little Red River downstream of Greers Ferry
Reservoir due to cold tailwater releases. The lake flooded optimal
habitat for the species, and caused the genetic isolation of
populations (McDaniel 1984, p. 1). The yellowcheek darter was known to
historically occur in portions of these streams that maintained
permanent year-round flows.
In the 1978-1981 study by Robison and Harp (1981, pp. 15-16),
yellowcheek darter occurred in greatest numbers in the Middle and South
Forks of the Little Red River, with populations estimated at 36,000 and
13,500 individuals, respectively, while populations in both Devils Fork
and Archey Fork were estimated at approximately 10,000 individuals
(Robison and Harp 1981, pp. 5-11). During this study, the four forks of
the Little Red River supported an estimated yellowcheek darter
population of 60,000 individuals, and the species was considered the
most abundant riffle fish present (Robison and Harp 1981, p. 14).
Extensive sampling of the first two tributaries of the Little Red River
below Greers Ferry Dam (both named Big Creek) failed to find any
yellowcheek darters, and no darters were found in immediately adjacent
watersheds (Robison and Harp 1981, p. 5).
Two subsequent studies have failed to observe yellowcheek darters
in the Turkey Fork reach of the Devils Fork Little Red River (Wine et
al. 2000, p. 9; Wine and Blumenshine 2002, p. 11), since four
individuals were last collected by Arkansas State University (ASU)
researchers in 1999 (Mitchell et al. 2002, p. 129). They have been
observed downstream within that system in the Beech Fork reach, where
flows are more permanent. The reach downstream of Raccoon Creek is
influenced by inundation from Greers Ferry Reservoir and no longer
supports yellowcheek darter. The U.S. Army Corps of Engineers
channelized approximately 5.6 km (3.5 mi) of the lower Archey and South
Forks Little Red River within the city limits of Clinton, Arkansas, in
1985 for flood control purposes. Yellowcheek darter has not been
collected within this reach since channelization. The yellowcheek
darter inhabits most of its historical range not currently affected by
Greers Ferry Lake, although in greatly reduced numbers in the Middle,
South, Archey, and Devils Forks of the Little Red River.
While collecting specimens for the 1999 genetic study, ASU
researchers discovered that the yellowcheek darter was no longer the
most abundant riffle fish and was more difficult to find throughout its
historical range (Wine et al. 2000, p. 2). Because optimal habitat had
been destroyed by the creation of Greers Ferry Lake, yellowcheek
darters were confined to upper stream reaches with lower summer flow,
smaller substrate particle size, and reduced gradient. A thorough
status survey conducted in 2000 found the yellowcheek darter in three
of four historically occupied forks in greatly reduced numbers (Wine et
al. 2000, p. 9). Populations in the Middle Fork were estimated at
approximately 6,000 individuals, the South Fork at 2,300, and the
Archey Fork at 2,000. Yellowcheek darter was not collected from the
Devils Fork. Fish community composition was similar from 1978-1981 and
2000 studies, but the proportion of yellowcheek darter declined from
approximately 28 percent to 6 percent of the overall composition. Fish
known to coexist with yellowcheek darter include the rainbow darter (E.
[[Page 48728]]
caeruleum) and greenside darter (E. blennioides), which can use pool
habitats during periods of low flow, as evidenced by the collection of
these two species from pools during electroshocking activities.
Electroshocking has not revealed yellowcheek darter in pools,
suggesting perhaps that they are unable to tolerate pool conditions
(deep, slow-moving water usually devoid of cobble substrate). An
inability to use pools during low flows would make them much more
vulnerable to seasonal fluctuations in flows that reduce riffle
habitat. As a result, researchers have suggested that yellowcheek
darter declines are more likely a species rather than community
phenomenon (Wine et al. 2000, p. 11).
Weston and Johnson (2005, p. 22) estimated yellowcheek darter
populations within the Middle Fork to be between 15,000 and 40,000
individuals, and between 13,000 and 17,000 individuals in the South
Fork. Such increases since the 2000 status survey would indicate
remarkable adaptability to changing environmental conditions. However,
it should be noted that estimates were based upon mark/recapture
estimates using the Jolly-Seber method, which requires high numbers of
recaptured specimens for accurate estimations. Recaptures were
extremely low during that study; therefore, population estimates were
highly variable and confidence in the resulting estimates is low.
The yellowcheek darter is ranked by the Arkansas Natural Heritage
Commission (ANHC) (2007, pp. 2-118) as an S1G1 species: extremely rare
in Arkansas, and critically imperiled globally. The Arkansas Game and
Fish Commission's (AGFC) Wildlife Action Plan describes the yellowcheek
darter as a critically imperiled species with declining populations
(AGFC 2005, pp. 452-454).
Chucky Madtom
The chucky madtom (Noturus crypticus) is a small catfish (family
Ictaluridae), with the largest specimen measuring 6.5 cm (2.6 in) SL
(Burr et al. 2005, p. 795). Burr et al. (2005) described the chucky
madtom, confirming previous analyses (Burr and Eisenhour 1994), which
indicated that the chucky madtom is a unique species, a member of the
Rabida subgenus (i.e., the ``mottled'' or ``saddled'' madtoms), and a
member of the Noturus elegans species complex (i.e., N. elegans, N.
albater, N. fasciatus, and N. trautmani) outlined by Taylor (1969 in
Grady and LeGrande 1992). A robust madtom, the chucky madtom body is
wide at the pectoral fin origins, greater than 23 percent of the SL.
The back contains three dark, nearly black blotches ending abruptly
above the lateral midline of the body, with a moderately contrasting,
oval, pale saddle in front of each blotch (Burr et al. 2005, p. 795).
The chucky madtom is a rare catfish known from only 15 specimens
collected from two Tennessee streams. A lone individual was collected
in 1940 from Dunn Creek (a Little Pigeon River tributary) in Sevier
County, and 14 specimens have been encountered since 1991 in Little
Chucky Creek (a Nolichucky River tributary) in Greene County,
Tennessee. Only 3 chucky madtom individuals have been encountered since
2000; 1 in 2000 (Lang et al. 2001, p. 2) and 2 in 2004 (CFI 2008,
unpublished data), despite surveys that have been conducted in both
historical localities at least twice a year since 2000 (Rakes and Shute
2004, pp. 2-3; Weber and Layzer 2007, p. 4; CFI 2008, unpublished
data). In addition, several streams in the Nolichucky, Holston, and
French Broad River watersheds of the upper Tennessee River basin, which
are similar in size and character to Little Chucky Creek, have been
surveyed with no success (Burr and Eisenhour 1994, pp. 1-2; Shute et
al. 1997, p. 5; Lang et al. 2001, pp. 2-3; Rakes and Shute 2004, p. 1).
Conservation Fisheries, Inc. did not find chucky madtoms in 2007 after
attempting new sampling techniques (e.g., PVC ``jug'' traps) (CFI 2008,
unpublished data).
Originally, museum specimens collected from the Roaring River in
Tennessee (Cumberland River drainage) and from Piney Creek, West Fork
Flint River, and the Paint Rock River system in Alabama (Tennessee
River drainage) were first identified and catalogued as Noturus elegans
species complex and thought to be chucky madtoms. The Roaring River,
Piney Creek, and West Fork Flint River specimens are now considered to
be a member of the N. elegans group, but have not been assigned to a
species. While the specimens from the Paint Rock River system share
typical anal ray counts with the chucky madtom, they lack the
distinctive cheek characteristics, differ in pelvic ray counts, and are
intermediately shaped between the chucky and saddled madtoms (N.
fasciatus) with respect to body width as a proportion of SL (Burr et
al. 2005, p. 796). Thus, the Little Chucky and Dunn Creek forms are the
only forms that are recognized as chucky madtoms.
All of the specimens collected in Little Chucky Creek have been
found in stream runs with slow to moderate current over pea gravel,
cobble, or slab-rock substrates (Burr and Eisenhour 1994, p. 2).
Habitat of these types is sparse in Little Chucky Creek, and the stream
affords little loose, rocky cover suitable for madtoms (Shute et al.
1997, p. 8). It is notable that intact riparian buffers are present in
the locations where chucky madtoms have been found (Shute et al. 1997,
p. 9).
No studies to determine the life history and behavior of this
species have been conducted. While nothing is known specifically about
chucky madtom reproductive biology, recruitment, growth and longevity,
food habits, or mobility, this information is available for other
similar members of the Noturus group. The least madtom (N. hildebrandi)
may reach sexual maturity at 1 or more years of age (i.e., during their
second summer) (Mayden and Walsh 1984, p. 351). Only the largest
females of Ozark madtom (N. albater) were found to be sexually mature,
and males were found to be sexually mature primarily within the second
age class (Mayden et al. 1980, p. 339), though, a single large male of
the first age class showed evidence of sexual maturity (Mayden et al.
1980, p. 339). The breeding season of the least and smoky madtoms (N.
baileyi) is primarily during June through July, though development of
breeding condition is initiated as early as April in least madtom and
May in smoky madtom (Mayden and Walsh 1984, p. 353; Dinkins and Shute
1996, p. 56). Fecundity varied among the species for which data were
available; however, it should be noted that fecundity in madtoms is
generally lower in comparison to other North American freshwater fishes
(Breder and Rosen 1966 in Dinkins and Shute 1996, p. 58). Dinkins and
Shute (1996, p. 58) commented that for smoky madtom the combination of
relatively large egg size and high level of parental care given to the
fertilized eggs and larvae reduce early mortality and, therefore, the
need to produce a large number of young.
Both smoky and elegant madtoms (N. elegans) were found to nest
under flat rocks at or near the head of riffles (Dinkins and Shute
1996, p. 56; Burr and Dimmick 1981, p. 116). Shallow pools were also
used by the smoky madtom, which was observed to select rocks of larger
dimension for nesting than were used for shelter during other times of
year (Dinkins and Shute 1996, p. 56). Single madtoms were found to
guard nests in smoky and elegant madtoms, a behavior also exhibited by
Ozark and least madtoms (Dinkins and Shute 1996, p. 56; Burr and
Dimmick 1981, p. 116; Mayden et al. 1980, p. 337;
[[Page 48729]]
Mayden and Walsh 1984, p. 357). Males of these species were the nest
guardians and many were found to have empty stomachs suggesting that
they do not feed during nest guarding, which can last as long as 3
weeks.
Conservation Fisheries, Inc. had one male chucky madtom in
captivity from 2004 through 2008. However, based on information from
other members of this genus for which longevity data are available,
least and smoky madtoms, it is unlikely that chucky madtoms can survive
this long in the wild. The shorter lived of these, least madtom,
reached a maximum age of 18 months, though most individuals lived
little more than 12 months, dying soon after reproducing (Mayden and
Walsh 1984, p. 351). Based on length-frequency distributions, smoky
madtoms exhibited a lifespan of 2 years, with two cohorts present in a
given year (Dinkins and Shute 1996, p. 53). Collection of two age
classes together provided evidence that life expectancy exceeds 1 year
in the pygmy madtom (N. stanauli) (Etnier and Jenkins 1980, p. 20). The
Ozark madtom lives as long as 3 years (Mayden et al. 1980, p. 337).
Chucky madtom prey items are unknown; however, least madtom prey
items include midge larvae, caddisfly larvae, stonefly larvae, and
mayfly nymphs (Mayden and Walsh 1984, p. 339). In smoky madtoms, mayfly
nymphs comprised 70.7 percent of stomach contents analyzed; fly,
mosquitoe, midge, and gnat larvae 2.4 percent; caddisfly larvae 4.4
percent; and stonefly larvae 1.0 percent (Dinkins and Shute 1996, p.
61). Significant daytime feeding was observed in smoky madtoms.
Dinkins and Shute (1996, p. 50) found smoky madtoms underneath
slabrocks in swift to moderate current during May to early November.
Habitat use shifted to shallow pools over the course of a 1-week
period, coinciding with a drop in water temperature to 7 or 8 [deg]C
(45 to 46 [deg]F), and persisted from early November to May. Eisenhour
et al. (1996, p. 43) collected saddled madtoms in gravel, cobble, and
slab-rock substrates in riffle habitats with depths ranging from 0.1 to
0.3 m (0.3 to 1.0 ft). Based on their limited number of observations,
Eisenhour et al. (1996, p. 43) hypothesized that saddled madtoms occupy
riffles and runs in the daylight hours and then move to pools at night
and during crepuscular hours (dawn and dusk) to feed.
The current range of the chucky madtom is believed to be restricted
to an approximately 3-km (1.8-mi) reach of Little Chucky Creek in
Greene County, Tennessee. Because this species was also collected from
Dunn Creek, a stream that is in a different watershed and physiographic
province than Little Chucky Creek, it is likely that the historic range
of the chucky madtom encompassed a wider area in the Ridge and Valley
and the Blue Ridge physiographic provinces in Tennessee than is
demonstrated by its current distribution. A survey for the chucky
madtom in Dunn Creek in 1996 was not successful at locating the species
(Shute et al. 1997, p. 8). The Dunn Creek population may be extirpated
(Shute et al. 1997, p. 6; Burr et al. 2005, p. 797), because adequate
habitat and a diverse fish community were present at the time of the
surveys, but no chucky madtoms were found. There are no population size
estimates or status trends for the chucky madtom due to low numbers and
only sporadic collections of specimens.
The chucky madtom is ranked by the TDEC (2009, p. 58) as an S1G1
species: extremely rare in Tennessee, and critically imperiled
globally. The chucky madtom is designated as a Tier 1 GCN species in
the Tennessee CWCS (TWRA 2005, pp. 44, 49).
Laurel Dace
The laurel dace (Chrosomus saylori), family Cyprinidae and
subfamily Leuciscinae, has two continuous black lateral stripes and
black pigment covering the breast and underside of the head of nuptial
(breeding) males (Skelton 2001, p. 120). The maximum SL observed is 5.1
cm (2 in) (Skelton 2001, p. 124). While the belly, breast, and lower
half of the head are typically a whitish-silvery color, at any time of
the year laurel dace may develop red coloration below the lateral
stripe that extends from the base of the pectoral fins to the base of
the caudal fin (Skelton 2001, p. 121).
Nuptial males often acquire brilliant coloration during the
breeding season, as the two lateral stripes, breast, and underside of
head turn intensely black and the entire ventral (lower/abdominal)
portion of the body, contiguous with the lower black stripe and black
breast, becomes an intense scarlet color. All of the fins acquire a
yellow color, which is most intense in the paired fins and less intense
in the dorsal, anal, and caudal fins. Females also develop most of
these colors, though of lesser intensity (Skelton 2001, p. 121).
Broadly rounded pectoral fins of males are easily discerned from the
broadly pointed fins of females at any time during the year.
Laurel dace have been most often collected from pools or slow runs
from undercut banks or beneath slab boulders, typically in first or
second order, clear, cool (maximum temperature 26 [deg]C or 78.8
[deg]F) streams. Substrates in streams where laurel dace are found
typically consist of a mixture of cobble, rubble, and boulders, and the
streams tend to have a dense riparian zone consisting largely of
mountain laurel (Skelton 2001, pp. 125-126).
Skelton (2001, p. 126) reported having collected nuptial
individuals from late March until mid-June, though Call (pers. obs.
2004) observed males in waning nuptial color during surveys on July 22,
2004. Laurel dace may be a spawning nest associate where syntopic
(sharing the same habitat) with nest-building minnow species, as has
been documented in blackside dace (Starnes and Starnes 1981, p. 366).
Soddy Creek is the only location in which Skelton (2001, p. 126) has
collected a nest-building minnow with laurel dace. Skelton (2001, p.
126) reports finding as many as three year classes in some collections
of laurel dace, though young-of-year fish are uncommon in collections.
Observations of three year classes indicate that laurel dace live as
long as 3 years.
Laurel dace preferred prey items include fly larvae, stonefly
larvae, and caddisfly larvae (Skelton 2001, p. 126). Skelton observed
that the morphological feeding traits of laurel dace, including large
mouth, short digestive tract, reduced number of pharyngeal (located
within the throat) teeth, and primitively shaped basioccipital bone
(bone that articulates the vertebra), all of which are consistent with
a diet consisting largely of animal material.
Laurel dace are known historically from seven streams on the Walden
Ridge portion of the Cumberland Plateau, where drainages generally
meander eastward before dropping abruptly down the plateau escarpment
and draining into the Tennessee River. Specifically, these seven
streams occur in three independent systems: Soddy Creek; three streams
that are part of the Sale Creek system (the Horn and Laurel branch
tributaries to Rock Creek, and the Cupp Creek tributary to Roaring
Creek); and three streams that are part of the Piney River system
(Young's, Moccasin, and Bumbee creeks). Strange and Skelton (2005, p.
8) assessed the genetic structure within populations of laurel dace
and, based on distribution of genetic diversity among populations, they
recognized two genetically distinct management units; (1) The southern
populations in Sale and Soddy Creeks, and (2) the northern population
in the Piney River system.
Skelton (2001, p. 126) considered collections by the Tennessee
Valley
[[Page 48730]]
Authority (TVA) during a rotenone survey of Laurel Branch in 1976 to
represent laurel dace that were misidentified as southern redbelly dace
(Chrosomus erythrogaster), as was found to be true for specimens
collected by TVA from Horn Branch in 1976, but no specimens are
available for confirmation. In 1991, and in four other surveys (two in
1995, one in 1996, and one in 2004), laurel dace were not collected in
Laurel Branch, leading Skelton to the conclusion that laurel dace have
been extirpated from this stream (Skelton 1997, p. 13; Skelton 2001, p.
126; Skelton pers. comm. 2009). Skelton (pers. comm. 2009) also noted
that the site was impacted by silt.
The current distribution of laurel dace comprises six of the seven
streams that were historically occupied; the species is considered
extirpated from Laurel Branch (see above). In these six streams, they
are known to occupy reaches of approximately 0.3 to 8 km (0.2 to 5 mi)
in length. The laurel dace is known from a single reach in Soddy Creek,
and surveys in 2004 produced only a single, juvenile laurel dace
(Strange and Skelton 2005, pp. 5-6 and Appendices 1 and 2). In Horn
Branch, laurel dace are known from approximately 900 m (2,953 ft), but
have become increasingly difficult to collect (Skelton 1997, pp. 13-
14). Skelton (1997, p. 14) reports that minnow traps have been the most
successful method for collecting live laurel dace from Horn Branch, as
it is difficult to electroshock the fish due to in-stream rock
formations and fallen trees. Only a single juvenile was caught in 2004
(Strange and Skelton 2005, p. 6). A total of 19 laurel dace were
collected from Cupp Creek during 1995 and 1996 using an electroshocker
(Skelton 1996, p. 14). However, Skelton found no laurel dace in this
stream in 2004, despite attempts to collect throughout an approximately
700-m (2,297-ft) reach (Strange and Skelton 2005, p. 6).
Laurel dace were initially found in Young's, Moccasin, and Bumbee
creeks in the Piney River system in 1996 (Skelton 1997, pp. 14-15).
Sampling in 2004 led to the discovery of additional laurel dace
localities in Young's and Moccasin creeks, but the locality where
laurel dace were found in Young's Creek in 1996 was inaccessible due to
the presence of a locked gate (Strange and Skelton 2005, p. 6-7). The
new localities were in the headwaters of these two streams. Persistence
of laurel dace at the Bumbee Creek locality was confirmed in 2004 by
surveying from a nearby road using binoculars. Direct surveys were not
possible because the land had been leased to a hunt club for which
contact information was not available, and, therefore, survey
permission could not be obtained (Strange and Skelton 2005, p. 7).
Nuptial males are easily identified from other species present in
Bumbee Creek due to their brilliant coloration during the breeding
season, as the two lateral stripes, breast, and underside of head turn
intensely black and the entire ventral (lower/abdominal) portion of the
body, contiguous with the lower black stripe and black breast, becomes
an intense scarlet color. This brilliant coloration is easily seen
through binoculars at short distances by trained individuals.
No population estimates are available for laurel dace. However,
based on trends observed in surveys and collections since 1991, Strange
and Skelton (2005, p. 8) concluded that this species is persisting in
Young's, Moccasin, and Bumbee creeks in the Piney River watershed, but
is at risk of extirpation from the southern part of Walden Ridge in
Soddy Creek, and in the Horn Branch and Cupp Creek areas that are
tributaries to Sale Creek. As noted above, the species is considered to
be extirpated from Laurel Branch, which is part of the Sale Creek
system.
The laurel dace is ranked by the TDEC (2009, p. 60) as an S1G1
species: extremely rare in Tennessee, and critically imperiled
globally. The laurel dace is designated as a Tier 1 GCN species in the
Tennessee CWCS (TWRA 2005, pp. 44, 49).
Summary of Comments and Recommendations
In the proposed rule published on June 24, 2010, we requested that
all interested parties submit written comments on the proposed rule to
list the Cumberland darter, rush darter, yellowcheek darter, chucky
madtom, and laurel dace by August 23, 2010. We also contacted
appropriate Federal and State agencies, scientific experts and
organizations, and other interested parties and invited them to comment
on the proposal. Newspaper notices inviting general public comment were
published in newspapers covering all affected counties in Kentucky,
Tennessee, Alabama, and Arkansas. We did not receive any requests for a
public hearing.
During the comment period for the proposed rule, we received ten
comment letters in response to the proposed rule: four from peer
reviewers, one from a State agency, and five from organizations or
individuals. All of the ten commenters supported the proposed rule to
list these five fishes as endangered. All substantive information
provided during the comment period has either been incorporated
directly into this final determination or is addressed below.
Peer Review
In accordance with our peer review policy published on July 1, 1994
(59 FR 34270), we solicited expert opinion from 12 knowledgeable
individuals with scientific expertise that included familiarity with
the 5 species and their habitats, biological needs, and threats. We
received responses from four of the peer reviewers.
We reviewed all comments received from the peer reviewers for
substantive issues and new information regarding the listing of the
five fishes. The peer reviewers generally concurred with our
conclusions and provided additional information on taxonomic
classification, life-history, and distribution; technical
clarifications; and suggestions to improve the final rule. Peer
reviewer comments are addressed in the ``Summary of Changes from
Proposed Rule'' and incorporated into the final rule as appropriate.
Public Comments
(1) Comment: Two commenters stated that the laurel dace is
threatened, particularly in Horn Branch, a tributary to the Rock Creek
watershed, by timber harvest, rock harvest (collection of surface
fieldstones), and coal mining of the Sewanee Coal Seam in Bledsoe and
Rhea counties, Tennessee. These commenters recommended critical habitat
designation in the Upper Rock Creek watershed of Bledsoe County,
Tennessee, due to the threats that are imminent and of high magnitude
in Horn Branch. The commenters are particularly concerned that mining
of the Sewanee Coal Seem would result in acid mine drainage.
Our Response: We concur with these commenters that the laurel dace
in Rock Creek watershed is threatened by timber harvest, rock harvest,
and coal mining. We have incorporated further analyses regarding the
threats of rock harvest and coal mining under ``Summary of Factors
Affecting the Species'' for laurel dace. Further analysis with regard
to critical habitat designation will be addressed in the upcoming
critical habitat rule.
(2) Comment: One commenter stated that the Cumberland darter is
threatened, particularly in Dan Branch, a tributary to the Lick Fork
watershed, by degradation of water quality from mountaintop mining
projects in Campbell and Claiborne counties, Tennessee. In addition to
this general concern, the commenter was aware of selenium contamination
within these same watersheds and feared that the
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issuance of new permits would cause further degradation to fish and
wildlife habitats in Campbell County.
Our Response: We concur with the commenter that mountaintop mining,
and specifically selenium contamination, has the potential to degrade
the water quality of Cumberland darter streams in Campbell and
Claiborne counties, Tennessee. Streams associated with mountaintop
mining and valley fills are characterized by increased conductivity,
total dissolved solids, and concentrations of sulfate, bicarbonate
ions, and metals such as manganese, iron, aluminum, and selenium.
Increased levels of selenium have been shown to bioaccumulate in
organisms, leading to deformities in larval fish and potentially
harming birds that prey on fishes. The proposed rule provided a more
detailed analysis of these and other water quality threats to the
Cumberland darter under ``Summary of Factors Affecting the Species.''
Summary of Changes From Proposed Rule
As a result of the comments received during the public comment
period (see above) we made the following changes to the final listing
rule:
(1) We added taxonomic classification information to the species'
background sections.
(2) We added life-history information to the Cumberland darter and
chucky madtom background sections.
(3) We updated the distributional information for the rush darter
in Alabama.
(4) We changed the genus of laurel dace from Phoxinus to Chrosomus
to reflect recent taxonomic changes (Strange and Mayden 2009).
(5) We updated population estimate and threats information for the
yellowcheek darter in Arkansas.
Summary of Factors Affecting the Species
Section 4 of the Act and its implementing regulations (50 CFR 424)
set forth the procedures for adding species to the Federal Lists of
Endangered and Threatened Wildlife and Plants. A species may be
determined to be an endangered or threatened species due to one or more
of the five factors described in section 4(a)(1) of the Act: (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; and (E) other natural or
manmade factors affecting its continued existence. Listing actions may
be warranted based on any of the above threat factors, singly or in
combination. Each of these factors is discussed below.
A. The Present or Threatened Destruction, Modification, or Curtailment
of Its Habitat or Range
The primary threat to the Cumberland darter, rush darter,
yellowcheek darter, chucky madtom, and laurel dace is physical habitat
destruction or modification resulting from a variety of human-induced
impacts such as siltation, disturbance of riparian corridors, and
changes in channel morphology (Waters 1995, pp. 2-3; Skelton 1997, pp.
17, 19; Thomas 2007, p. 5). The most significant of these impacts is
siltation (excess sediments suspended or deposited in a stream) caused
by excessive releases of sediment from activities such as resource
extraction (e.g., coal mining, silviculture, natural gas development),
agriculture, road construction, and urban development (Waters 1995, pp.
2-3; Kentucky Division of Water (KDOW) 2006, pp. 178-185; Skelton 1997,
pp. 17, 19; Thomas 2007, p. 5).
Land use practices that affect sediment and water discharges into a
stream can also increase the erosion or sedimentat