Notropis
potteri
chub shiner
Type Locality
Waco Creek, near Waco,
McLennan Co., TX (Hubbs and Bonham 1951).
Etymology/Derivation of Scientific Name
Named after the first collector, naturalist Dr. George E. Potter of Baylor
University and Texas A&M University (Hubbs and Bonham 1951).
Synonymy
Common name was originally Potter’s minnow (Potter 1938:423).
Characters
Maximum size: 110 mm
(4.33 in) TL (Page and Burr 1991).
Life colors:
Moderately dusky above and silvery below, with little pigment below the
region of the lateral line. Melanophores scattered evenly on upper parts of
the head and body. Large melanophores dispersed about the lateral line
anteriorly. Dark lateral band moderately developed on the caudal peduncle,
ending just before the weak and diffuse basicaudal spot (Hubbs and Bonham
1951).
Pharyngeal teeth count:
2, 4-4, 2 or 1,4-4,1; pharyngeal teeth in lesser row stout (Hubbs and Bonham 1951;
Hubbs et al. 1991).
Counts: 34-37 lateral
line scales; dorsal fin soft rays 8 (7-8); anal fin soft rays 7 (6-8) (Hubbs and
Bonham 1951;
Hubbs et al. 1991).
Body shape:
Moderately large, slim; broad head (Robison and Buchanan 1988). .
Mouth position:
Terminal and oblique; lower lip thin without a fleshy lobe (Hubbs et al.
1991). Middle part of lower lip and the
posterior part of the upper lip are swollen (Hubbs and Bonham 1951).
Large mouth with a mean (±SD) relative gape size (gape / total
length) of 7.2% (±0.41) (J. Perkin et al., Texas State University,
unpublished data).
Morphology:
Eye small, contained about four times in body depth, measured over curve
(Hubbs et al. 1991). Body depth contained four and one-quarter times
in standard length; depth at occiput
equal to or less than width at occiput. Lateral line complete either straight or with a
broad arch; premaxillaries protractile; upper lip separated from skin of snout by a
deep groove continuous across the midline; distance from origin of anal fin to end of caudal peduncle
contained two and one-half or fewer times in
distance from tip of snout to origin of anal fin (Hubbs et al. 1991). Rigid
lateral projection of pectoral fins; adaptation for benthic habitats
(Suttkus and Clemmer 1968). Intestinal canal short, forming a simple S-shaped loop (Hubbs et al. 1991).
Distribution (Native and Introduced)
U.S. distribution:
Red, Muddy Boggy and Kiamichi rivers of Oklahoma (Hubbs and Bonham 1951,
Pigg 1977, Miller 1979; Taylor et al. 1996); Red River of Arkansas (Robinson
1974); Mississippi River and Atchafalaya
River in Louisiana (Douglas 1974; Schramm 2004; Suttkus and Clemmer 1968);
several drainages in Texas (Gilbert 1980).
Texas distribution:
Brazos River, Colorado River, San Jacinto River, Trinity Rivers, and
Galveston Bay, Texas (Hubbs and Bonham 1951, Jurgens 1954, Blair et al.
1957, Conner 1977). According to Hubbs et al. (1991), species ranges
throughout the Brazos and Red basins; population also known from the San
Jacinto Drainage near Conroe. Warren et al. (2000) listed the following
drainage units for distribution of N. potteri in the state: Red
River (from the mouth upstream to and including the Kiamichi River),
Galveston Bay (including minor coastal drainages west to mouth of Brazos
River), Brazos River, Colorado River.
Originally described as an
endemic to the Brazos River drainage; populations elsewhere were introduced
by bait bucket releases (Hubbs and Bonham 1951, Hall 1956). Others recognize
Brazos River as location of origin but claim that N. potteri
occurrence elsewhere is natural, disputing the bait bucket release
explanation (Miller 1953, Suttkus and Clemmer 1968, Conner 1977). Recent
work by Perkin et al. (unpublished data) suggests that N. potteri
should be considered native to drainages other than the Brazos River.
[Additional literature
noting collection of this species from Texas locations includes, but is not
limited to the following: Riggs and Bonn (1959); Stevenson et al.
(1974); Hubbs and Dean (1979); Winston (1995); Lienesch and Matthews (2000);
Lienesch et al. (2000); Gido et al. (2002); Ostrand and Wilde (2002);
Winemiller et al. (2004); Zeug et al. (2005).]
Abundance/Conservation status (Federal, State,
Non-governmental organizations)
Currently stable (Warren et
al. 2000), especially in the Red River downstream from Lake Texoma (Perkin
et al., unpublished data). Brazos River population is declining in the
upper (G. Wilde, Texas Tech University, personal communication) and lower
reaches (Runyan and Bonner 2007). Notropis potteri is susceptible to
extirpation by damming (Winston et al. 1991).
Habitat Associations
Macrohabitat: Large,
turbid rivers (Gilbert 1980); also found in smaller tributaries (Hubbs and
Bonham 1951).
Mesohabitat: Found in
flowing water with silt or sand substrate (Gilbert 1980; Perkin et al.
unpublished data). Tolerant of high salinities (Taylor et al. 1993; Higgins
and Wilde 2005); Echelle et al. (1972) reported collection of species at
salinities ranging from 4.2-19.7 ppt.
Biology
Spawning season: Males
with mature testes from March through September; one sexually developing
female found in May; one sexually mature female found in August (Perkin et
al., unpublished data)
Spawning location: No
information at this time.
Reproductive strategy:
Likely a broadcast spawning pelagophil.
Fecundity: Only sexually mature female
49 mm (1.93 in) TL captured from the Brazos River had 120 vitellogenic oocytes in
left ovary (estimated 240 overall) (Perkin et al., unpublished data).
Age at maturation:
Likely one year
Migration: No
information at this time.
Growth and population
structure: Age 0 up to 45 mm (1.77 in); age 1 up to 70 mm (Perkin
et al., unpublished data)
Longevity: Age 2 (Perkin
et al., unpublished data)
Food habits:
Invertivore and piscivore; gut contents of fish captured from Oklahoma and
Louisiana consisted of 63% benthic invertebrates (by volume), 13% fish, 16%
substrate particles (probably ingested accidentally), and 8% open water
invertebrates (mostly Cladocera; Felly 1984). Gut contents of fish captured
from the lower Brazos River consisted of aquatic insects (40%) and fish
(28%); Coleoptera and Tricoptera were most abundant aquatic insects; red
shiners (Cyprinella lutrensis) and western mosquitofish (Gambusia
affinis) were common fish prey (Perkin et al.,
unpublished data).
Phylogeny and morphologically similar fishes
Subgenus Alburnops. Similar
species include the smalleye shiner (Notropis buccula), and the Red River
shiner (N. bairdi), which differ from N. potteri in having black
specks concentrated in patch on side, eye directed more to side than
upwardly, shorter snout, pharyngeal teeth 0,4-4,0; and the river shiner (N. blennius) which has larger eye located more on side of head, duskier
back and side, more pointed snout (Page and Burr 1991). See Hubbs and Bonham
(1951) for further comparison with N. bairdi, and N. blennius.
N. potteri differs from the Sabine shiner (N. sabinae) in that
it is a much larger and coarser fish, with somewhat smaller and much less
inferior and less horizontal mouth, and in the dental formula 2,4-4,2
(versus 0,4-4,0 or 1,4-4,1); differs from the Arkansas River shiner (N.
girardi) in having 2,4-4,2 dental formula as opposed to 0,4-4,0 (Hubbs and Bonham 1951).
Host Records
No information
at this time.
Commercial or Environmental Importance
Species potentially
vulnerable to extinction in the event of major global warming (of 3-4°C),
and without population having avenue for northward dispersal (Matthews and
Zimmerman 1990).
References
Conner,
J.V. 1977. Zoogeography of freshwater fishes in western Gulf Slope drainages
between the Mississippi and The Rio Grande. Ph.D. Dissertation. Tulane
University, New Orleans, LA. 269 pp.
Douglas,
N.H. 1974. Freshwater Fishes of Louisiana. Claitor’s Publishing Division,
Baton Rouge, Louisiana. 443 pp.
Echelle,
A.A., A.F. Echelle, and L.G. Hill. 1972. Interspecific interactions and
limiting factors of abundance and distribution in the Red River pupfish,
Cyprinodon rubrofluviatilis. American Midland Naturalist 88(1):109-130.
Felley, J.D. 1984. Piscivorous habits of the chub shiner, Notropis
potteri (Cyprinidae). Southwestern Naturalist 29:495-496.
Gido, K.B., C.W. Hargrave, W.J. Matthews, G.D. Schnell, D.W. Pogue, and G.W.
Sewell. 2002. Structure of littoral-zone fish communities in relation to
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