Opsopoeodus emiliae
pugnose minnow
Type Locality
Horsehunter Creek, near
confluence Noxubee County, Macon, Noxubee Co., Mississippi (Hay 1881).
Etymology/Derivation of Scientific Name
Opsopoeodus, Greek,
“teeth for dainty feeding;” emiliae, named for Emily Hay (Pflieger
1997), wife of Dr. Oliver P. Hay. Hay (1881) stated that the name
Opsopoeodus “is given in allusion to the throughness with which the food
is prepared by the numerous serrated pharyngeal teeth.”
Synonymy
Species transferred from the
monotypic genus Opsopoeodus to Notropis by Gilbert and Bailey
(1972). This transfer was disputed by Campos and Hubbs (1973) on the basis
of chromosomal count, the authors considered the karyotype of the species
distinctive enough to warrant continued recognition of Opsopoeodus as
a genus.
Opsopoeodus emilae Hay
1881:507, 1883:72; Cook 1959:101; Medford and Simco 1971:122
Notropis emiliae
Pierson and Schultz 1984:3; Hubbard 1987:23; Knight and Cooper 1987:33;
Mettee et al. 1987:99, 1989:60.
Characters
Maximum size: 55 mm
(2.17 in) SL
(Edwards 1997).
Life colors:
Crosshatch pattern on back and upper half to all of side; two dark areas
(front and rear – clear area between) on dorsal fin, most prominent on large
male; dusky olive-yellow above; dark stripe along silver side of head and
body, sometimes ending in small black spot on caudal fin base; breeding male
has bright white lower half of anal and pelvic fins (Page and Burr 1991).
Males develop small white knobs on the first three dorsal rays (Page and
Johnston 1990).
Pharyngeal teeth count:
0,5-5,0 or
0,5-4,0 (Hubbs et al. 2008).
Counts: 16-18 (15-21)
predorsal diagonal scale rows; circumferential body scale rows are 26
(23-27), with 13 above and 11 below the lateral line; 38-39 (36-42) lateral
line scales; 7-9 gill rakers (total); 9 dorsal fin soft rays, 8 anal fin
soft rays, 14-15
(12-16) pectoral soft fin rays, and 8 pelvic soft fin rays (Ross 2001).
Body shape: Slender,
laterally compressed with short head; blunt snout (Ross 2001).
Mouth position:
Oblique (Ross 2001), almost vertical (Hubbs et al 1991).
Morphology: Lateral
line straight and usually completely pored, sometimes incomplete on the
caudal peduncle (Ross 2001). Mouth very small. 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); small crowded scales on front half of
nape (Page and Burr 1991). Males develop small white knobs on the first
three dorsal rays, which likely function as egg mimics that help to
stimulate the female to spawn (Page and Johnston 1990).
Distribution (Native and Introduced)
U.S. distribution:
Found throughout the Mississippi Valley (Hubbs et al 1991).
Texas distribution:
Primarily in streams of the Coastal Plain; a record of this species in the
Trinity River near the Dallas area (Hubbs et al 1991).
[Additional literature
noting collection of this species from Texas locations includes, but is not
limited to the following: Brazos River (Winemiller et al. 2004); (Hubbs
1957); Navasota River (Brazos Co.; Schmidt et al. 1998).]
Abundance/Conservation status (Federal, State,
Non-governmental oganizations)
Populations in the southern
United States are currently secure (Warren 2000).
Habitat Associations
Macrohabitat: Usually
in slow-moving rivers and streams (Hubbs et al 1991); Quiet, weedy backwater
areas of lakes, swamps, oxbows (Gilbert and Bailey 1972; Trautman 1981; Page
and Burr 1991). Moriarty and Winemiller (1997) collected individuals mainly
in backwater habitats in Village Creek, Texas.
Mesohabitat: More
common in clear than turbid waters; strongly associated with emergent and
submerged aquatic vegetation (Gilbert and Bailey 1972; Trautman 1981);
collected in clear water environments in the Colorado River between Austin,
Texas and Bastrop, Texas
(Edwards 1997).
Biology
Spawning season: In
Florida, late winter into late summer (McLane 1955). In Illinois, spawning
fish collected in May and June (Gilbert and Bailey 1972). In Texas, minnows
collected showing length-frequency distributions consistent with late
spring-early summer (May-June) spawning (Moriarty and Winemiller 1997).
Based on the presence of small specimens, less than 16 mm SL, from March
through July (housed in various research museums) Edwards (1997) suggests a
spawning season, in Texas, from late February through at least the summer.
Spawning location:
Known to be underneath flat rocks, in cavities (Page and Johnston 1990)
Reproductive strategy:
Nest spawner; speleophil (Simon 1999). Territorial in spawning sites; eggs
are laid singly or in strings on the underside of rock, then fertilized by male; males courts with lateral displays
and leading behavior by swimming back and forth from female to nesting site;
several females may contribute to one male's egg mass; females leaves site
and male remains to aerate and guard the eggs (Page and Johnston 1990)
Fecundity: A female
can lay from 30 to 120 eggs every six or seven days; fertilized,
water-hardened eggs 1.1-1.5 mm (0.04-0.59 in) in diameter; eggs incubated in
laboratory conditions hatch successfully in 142 hours at 21°C, and in 90 hours
at 27°C; newly hatched larvae 5-5.5 mm (0.20-0.22
in) long (Page and Johnston
1990).
Age at maturation:
Probably reached in first year (Boschung and Mayden 2004).
Migration: No
information at this time.
Longevity: Maximum
life span is likely two to three years (Becker 1983).
Food habits:
Detritivore; particulate feeder; scooper (Simon 1999). Midge larvae,
filamentous algae, small crustaceans, water mites, larval
fishes, and fish eggs (McClane 1955; Becker 1983). Based on mouth shape
feeding likely occurs in midwater or near surface; serrations on pharyngeal
teeth apparently adaptation to feeding habits, particularly the consumption
of microcrustaceans (Gilbert and Bailey 1972).
Growth:
Individuals reach approximately 35 mm (1.38 in) SL after their first year of growth
(Edwards 1997). Larval development described by Millard (1981):
protolarvae are 5.7-7.8 mm (0.22-0.31 in) TL, mesolarvae are 6.6-8.8 mm
(0.26-0.35 in) TL; all
principal caudal rays are complete in larvae greater than 8.64 mm (0.34 in) TL, and
full complement of median rays are present by 9.23 mm (0.36 in) TL; middorsal stripe
begins development by 12.0 mm (0.47 in) TL.
Phylogeny and morphologically similar fishes
Opsopoeodus emiliae
resembles the taillight shiner (N. maculatus), the two occurring in similar habitats, but
they are distinguished by the characteristic mouth, 9 dorsal rays, and
pharyngeal tooth count (usually 0,5-5,0) of O. emiliae; N.
maculatus has a prominent caudal spot which is lacking in O. emiliae
(Boschung and Mayden 2004).
Host Records
Trematoda :
Posthodiplostomum minimum (Hoffman 1967).
Commercial or Environmental
Importance
In Mississippi, where the
species is locally common, it is used as a bait minnow (Cook 1959).
References
Becker, G. C. 1983. Fishes of Wisconsin. Univ. of Wisconsin Press, Madison
1052 pp.
Boschung, H.T., Jr., and R.L. Mayden. 2004. Fishes of Alabama. Smithsonian
Books, Washington. 736 pp.
Campos, H.H., and C. Hubbs. 1973. Taxonomic implications of the karyotype of
Opsopoeodus emiliae. Copeia 1973(1):161-163.
Cook, F. A. 1959. Freshwater fishes in Mississippi. Mississippi Game and
Fish Commission, Jackson.
Edwards, R. J. 1997. Ecological profiles for selected stream-dwelling Texas
freshwater fishes. Report to the Texas Water Development Board. 89 pp.
Gilbert, C.R. 1980. Notropis emiliae (Hay), Pugnose minnow. p.262
in D.S. Lee, et al. Atlas of North American Freshwater Fishes. N.C.
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American cyprinid fish Notropis (Opsopoeodus) emiliae.
Occ. Pap. Mus. Zool. Univ. Univ. Mich. 664:1-35.
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U.S. Nat. Mus. 3:488-515.
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