Elassoma zonatum
banded pygmy sunfish
Type Locality
Little Red River, White Co.,
Arkansas, and Rio Brazos, Texas (Jordan 1877).
Etymology/Derivation of Scientific Name
Elassoma, Greek,
meaning “small”; zonatum, Latin, meaning “banded” (Pflieger 1975).
Synonymy
Elassoma zonatum
Jordan 1877:50; Hay 1881:500, 1883:74; Hildebrand and Towers 1928:135.
Ellasoma zonatum Cook 1959:172
Characters
Maximum size: 44.6 mm
TL (Walsh and Burr 1984).
Life colors: The back
and sides are brown with 9-12 dark brown or blue black on the sides just
above the pectoral fin. The undersides of the head and body have numerous
melanophores. The preorbital, post orbital, and suborbital bars are
generally well developed. The dorsal and anal fins have irregular bars, and
the pelvic and caudal fins are spotted. The pectoral fin is generally clear,
except for fine melanophores along the fin rays. Breeding males are very
dark and have numerous black spots on the head and iridescent blue patches
below the eye, on the opercle, and on the base of the pectoral fin. There
are gold flecks over the head and trunk (Ross 2001).
Counts: 4-5 dorsal
fin spines; 5 brachiostegals (Hubbs et al. 1991). Lateral series 31-36;
dorsal fin with 4-5 spines and 9-10 soft rays; anal fin with 3 spines and
6-5 soft rays; pectoral fin short and rounded, with 14-17 rays; pelvic fin
with 1 spine and five rays; principal caudal fin rays 13-16; gill rakers 6-8
and about as wide as long (Etnier and Starnes 1993).
Body shape: Small,
shallow-bodied, laterally compressed fish (Ross 2001); jaws with tiny
conical teeth (Etnier and Starnes 1993).
Mouth position:
Terminal (Goldstein and Simon 1999).
External morphology:
Lateral line absent; scales cycloid (Hubbs et al. 1991).
Distribution (Native and Introduced)
U.S. distribution:
Wide-ranging species occuring in lowland streams of the Atlantic and Gulf
costal plains (Hubbs et al. 1991).
Texas distribution:
Inhabits eastern Texas from the Red River southward to the Brazos River
Basin (Hubbs et al. 1991).
Abundance/Conservation status (Federal, State, NGO)
Not listed as threatened or
endangered by Texas Parks and Wildlife Department
(2006). Populations in the
southern United States are currently secure (Warren et al. 2000).
Habitat Associations
Macrohabitat:
Throughout range, E. zonatum frequents lentic waters such as cypress
swamps, lake margins, sloughs, sluggish streams, and lowland backwaters
(Barney and Anson 1920; Branson 1974; Coker 1917; Gunning and Lewis 1955;
Warren 1980).
Mesohabitat: Prefers
clear quiet water with thick growths of submerged vegetation (Böhlke and
Rhode 1980) and protective cover such as logs, stumps, cypress knees,
overhanging banks over soft substrates (Barney and Anson 1920; Branson 1974;
Coker 1917; Gunning and Lewis 1955; Warren 1980). Tolerant of low-salinity
water (Hoese and Moore 1977). In collections from Village Creek (tributary
of the Neches River),Hardin County, Texas, E. zonatum captured from
the channel edge during summer and from backwaters during fall; species
preferring shallow water with macrophytes and leaf litter; this habitat
almost disappearing from the channel area during high discharge, perhaps
explaining why the species was not collected during winter and spring
(Moriarty and Winemiller 1997). During November sampling in Allens Creek
(small tributary of Brazos River), in Austin County, Texas, E. zonatum
specimen was found in turbid water over very soft sand/silt substrate;
willows dominated stream bank cover; very little instream cover was noted
(Linam et al. 1994).
Biology
Spawning season:
Mid-March-early May (Barney and Anson 1920); March-June (Walsh and Burr
1984).
Spawning habitat:
Near submerged vegetation (Walsh and Burr 1984). Guarders; substratum
choosers; Phytophils having adhesive eggs that are attached to a
variety of plants (Mettee 1974; Simon 1999).
Reproductive strategy:
Males establish territories around submerged vegetation and will defend this
area from other males and nonreceptive females by lateral displays (Walsh
and Burr 1984). Males do not excavate a nest
(Barney and Anson 1920). Courtship involves erecting the fins, alternatively
erecting and lowering the pelvic fins, bobbing, and lateral fin undulations
(Walsh and Burr 1984). After attracting female, the male coaxes her toward
an area over vegetation, then nudges female near the vent area; eggs
expelled in short bursts and fertilized by male; females spawn repeatedly
until all mature ova are deposited, fewer eggs released with each successive
spawning (Barney and Anson 1920). After spawning the female is chased from
the area by the male; male then guards the developing embryos for up to 48
hours (Walsh and Burr 1984).
Fecundity: Eggs are
demersal, adhesive, and usually 0.5 mm diameter; a single female may contain
96-970 eggs; average size female (25 mm) lays about 300 eggs over several
days in lots of 60 to 40; incubation time about 7 days at water temperature
of 18.5 degrees C (Barney and Anson 1920).
Walsh and Burr (1984) reported 6-76 amber colored, demersal, adhesive eggs
laid per spawning act; eggs reticulated on the surface; number of
potentially mature ova in preserved females was 43-255; hatching occurred in
97-116 hrs. at water temperature of 21 ± 1 degree C.
Age at maturation:
10-12 months; age at first spawning 1 year (Walsh and Burr 1984).
Migration:
Longevity: Up to 3
years, but typically only about one year (Barney and Anson 1920; Walsh and
Burr 1984).
Food habits:
Invertivore, drift feeder, feeding in the water column; main food
microcrustacea supplemented with midge larvae, large crustacean (amphipods
and isopods), mayfly nymphs, and small snails and clams (Barney and Anson
1920; Walsh and Burr 1984; Goldstein and Simon 1999).
Feeding is cued visually with peak activity immediately following
sunrise and a secondary peak at midday (Walsh and Burr 1984).
Growth: Newly
hatched protolarvae ranged in length from 3.0-3.6 mm TL; major organogenesis
and yolk reabsorption were complete in 5-7 days post-hatching (Walsh and
Burr 1984). During the spring and summer, growth is rapid with fish reaching
half their first year’s growth in eight weeks. Fish average 22.9mm SL and
30.2mm SL at the end of year 1-2, respectively (Barney and Anson 1920).
Phylogeny and morphologically similar fishes
Pygmy sunfish are unlikely to
be confused with other fishes, although at first glance could be mistaken
for pirate perch. Their small size, absence of a lateral line, cycloid
scales and low number of dorsal spines (three to five versus six or more)
distinguish them from sunfishes and basses. They differ from pirate perch in
having an abdominal versus jugular vent position and in having cycloid
scales (Ross 2001).
Host Records
Rhipidocotyle
septapapillata, Camallanus oxycephalus, Hedrurus (Mayberry
et al. 2000). Gyrodactylus heterodactylus (Harris et al 2004).
Nematoda (Hoffman 1967).
Commercial or Environmental Importance
[Additional literature
noting collection of this species from Texas locations includes, but is not
limited to the following: Hubbs (1957); Big Sandy Creek (Evans and Noble
1979).]
References
Barney, R.L. and B.J. Anson. 1920. Life history and ecology of the pigmy
sunfish Elassoma zonatum. Ecology 1(4):241-256.
Böhlke, J.E. and Rhode F.C. 1980. Elassoma zonatum (Jordan), Banded
pygmy sunfish. pp. 586 in D.S. Lee et al. Atlas of North American
Freshwater Fishes. N.C. State Mus. Nat. Hist., Raleigh, i-r+854 pp.
Branson, B.A. 1974. Pygmy sunfish for community aquaria. Tropical Fish
Hobbyist 22(10):17-22.
Coker, A.F., Jr. 1917. The pygmy sunfishes. Aquatic Life 3(2):22-24.
Cook, F.A. 1959. Freshwater fishes in Mississippi. Mississippi Game and Fish
Commision, Jackson.
Etnier, D.A., and W.C. Starnes. 1993. The Fishes of Tennessee. University of
Tennessee Press, Knoxville. 681 pp.
Evans, J.W., and R.L. Noble. 1979. The longitudinal distribution of fishes
in an east Texas stream. American Midland Naturalist 101(2):333-343.
Goldstein, R.M., and T.P. Simon. 1999. Toward a united definition of guild
structure for feeding ecology of North American freshwater fishes. pp.
123-202 in T.P. Simon, editor. Assessing the sustainability and
biological integrity of water resources using fish communities. CRC Press,
Boca Raton, Florida.
Gunning, G.E., and W.M. Lewis. 1955. The fish population of a spring-fed
swamp in the Mississippi bottoms of southern Illinois. Ecology
36(4):552-558.
Harris, P.D., A.P.Shinn, J. Cable and T.A. Bakke. 2004. Nominal species of
the genus Gyrodactylus von Nordman 1832 (Monogenea: Gyrodactylidae),
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U.S. Nat. Mus. 3:488-515.
Hay, O.P. 1883. On a collection of fishes from the lower Mississippi Valley.
Bull. U.S. Fish Comm. 2:57-75.
Hildebrand, S.F. and I.L. Towers. 1928. Annotated list of fishes collected
in the vicinity of Greenwood Mississippi, with descriptions of three new
species. Bull. U.S. Bur. Fish. 43(2)105-136.
Hoese, D.H., and R.H. Moore. 1977. Fishes of the Gulf of Mexico (Texas,
Louisiana, and Adjacent Waters). Texas A&M University Press. xv + 327 pp.
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of California Press. Berkeley and Los Angeles, CA 1-486.
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freshwater fishes of Texas, with key to identification of species. Texas
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Jordan, D.S. 1877. Contributions to North American ichthyology, based
primarily on the collections of the United States National Museum. No. 2A.
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Centrarchidae, Aphredoderidae, Dorysomatidae, and Cyprinidae,
with revisions of genera and descriptions of new or little known species.
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Linam, G.W., J.C. Henson, and M.A. Webb. 1994. A fisheries inventory and
assessment of Allens Creek and the Brazos River, Austin County, Texas. River
Studies Report No. 12. Resource Protection Division. Texas Parks and
Wildlife Department, Austin. 14 pp.
Mayberry, L. F., A.G. Canaris, J.R. Bristol, and S.L. Gardner. 2000.
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Texas (1893-1984). University of Nebraska Harold W. Manter Laboratory of
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Unpublished PhD. Dissertation. University of Alabama, Tuscaloosa.
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22:88-151.
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