Aplodinotus grunniens
freshwater drum
Type Locality
Ohio River (Rafinesque 1819).
Etymology/Derivation of Scientific Name:
Aplodinotus, Greek,
meaning “single back,” in reference to the dorsal fin; grunniens,
Latin, meaning “grunting,” in reference to sounds production in this species
(Pflieger 1997) .
Synonymy
Aplodinotus grunniens
Rafinesque 1819:418; Hildebrand and Towers 1928:135; Cook 1959:211.
Amblodon Wailes
1854:333.
Haploidontus grunniens
Hay 1883:64.
Characters
Maximum size: 696 mm
TL (Wrenn 1969).
Coloration: Monotone
silver; Dorsal and caudal fins outlined with black pigments.
Pharyngeal teeth count:
NA
Counts: Fewer than 60
lateral line scales (Hubbs et al. 1991); 10
dorsal spines; 30 dorsal rays; 20-24 gill rakers (Knapp 1953); 2 anal
spines; 6-7 anal rays; 15-16 pectoral rays; 1 pelvic spine; 5 pelvic rays
(Ross 2001).
Body shape: Strongly
arched body, laterally compressed.
Mouth position:
Subterminal (Goldstein and Simon 1999).
External morphology:
Shortest dorsal spine <1/2 of longest dorsal spine, forming a distinct, deep
notch between spiny dorsal fin and soft dorsal fin rays. Anteriorly-arched
lateral line extends into caudal fin.
Distribution (Native and Introduced)
U.S. distribution:
Central North America from Canada to Central America (Hubbs et al. 1991).
Apparently has greatest latitudinal range of any North American
freshwater fish (Fremling 1980).
Texas distribution:
Widely occurring except in the Panhandle region (Hubbs et al. 1991). Warren
et al. (2000) listed the following drainage units for distribution of
Aplodinotus grunniens in the state: Red River (from the mouth upstream
to and including the Kiamichi River), Sabine Lake (including minor coastal
drainages west to Galveston Bay), Galveston Bay (including minor coastal
drainages west to mouth of Brazos River), Brazos River, Colorado River, San
Antonio Bay (including minor coastal drainages west of mouth of Colorado
River to mouth of Nueces River), Nueces River.
Abundance/Conservation status (Federal, State, NGO):
Currently stable in southern
US (Warren et al. 2000). Edwards and Contreras-Balderas (1991) reported a
general decline of this species in the lower Rio Grande in the last 100-year
period.
Habitat Associations
Macrohabitat: Turbid
to clear lakes and rivers, but does occur in a wide variety of habitats (Fremling
1980).
Mesohabitat: Benthic
habitats of large, shallow bodies of water (to 40-60 feet; Scott and
Crossman 1973). More commonly associated with large woody debris than open
areas in Kansas reservoir (Willis and Jones 1986). In large rivers, fish may
move distances of at least 161 km (Funk 1955). In Lake Texoma
(Oklahoma-Texas), larvae responded to increased turbidity by moving up near
the surface, instead of remaining in deep water during daylight hours, as
typical (Matthews 1984). Gido and Matthews (2000) reported marked seasonal
abundance patterns for large fish in Lake Texoma (Oklahoma-Texas), with peak
in abundance during warm seasons; the abundance of juvenile (< 200 mm SL)
fish increased during summer; also, large fish increased in relative
abundance during increased periods of reservoir volume. Riggs and Bonn
(1959) noted that the species was fairly common in most deeper parts of Lake
Texoma (Oklahoma-Texas), and was abundant in the tail waters. Li (2003)
reported that the species was commonly collected in deepwater sites of the
lower Brazos River, Texas, during summer and winter seasons; was positively
associated with conductivity and strongly associated with summer samples.
After reaching 25 mm in length, fish are found on or near bottom (Priegel
1967b). Individuals have been observed to become distressed when water
temperatures exceed 25.6°C, and when dissolved oxygen concentrations remain
low over an extended period (Priegel 1967b).
Biology
Spawning season: In
May and June, usually at water temperatures between 18-26°C (Wrenn 1969;
Swedberg and Walburg 1970; Fremling 1980).
Spawning location:
Open water. In the Upper Mississippi River, eggs and larvae were abundant
in the main channel collections (Holland 1986).
Reproductive strategy:
Nonguarders; open substratum spawners; pelagophils – characterized by
numerous buoyant eggs (Simon 1999). Eggs and sperm released in the water
column; eggs are buoyant, larvae are planktonic (Daiber 1953). Males “drum”
communicate to form spawning aggregates by vibrating specialized muscles
against gas bladder (Fremling 1980); only sexually mature males possess this
structure, which may be fully developed by the third year of life (Priegel
1967b).
Fecundity: 600,000
eggs for large females (3.5 kg; Wrenn 1969; Fremling 1980).
Number of vitellogenic oocytes ranged from 34,000 to 66,500, in 6-9
year-old fish measuring from 307-386 mm long; egg diameters post
fertilization ranged from 1.39 to 1.57 mm; hatching occurred in 27 hours at
a water temperature of 23°C (Swedberg and Walburg 1970).
Large-yolked, unfertilized eggs from a mature 5-year-old female
averaged 0.72 mm in diameter (Daiber 1953).
Age/Size at maturation:
Ages 4 to 6, with males measuring at least 203 mm TL and females 221 mm TL
(Diaber 1953; Priegel 1969; Wrenn 1969). Dryer (2007) reported that
maturation occurred most often during years 3 – 4, in Alabama populations.
Migration: NA
Longevity: Rypel
(2007) reported males up to 21 years and females up to 32 years in Alabama
populations.
Food habits:
Primarily a benthic feeder, consuming insect larvae, crustaceans, fish,
clams, and snails; molar-like pharyngeal teeth aid in masticating mollusks
(Fremling 1980). Consumes mayflies and
amphipods; fish and crayfish appear more frequently in diet of larger
individuals (Daiber 1952). In Lake Winnebago, Wisconsin, midge larvae was
main food item in diet of fish over 40 mm (1.6 inches), and copepods (Cyclops)
were main food item for fish under 40 mm (1.6 inches; Preigel 1967a). In
Lewis and Clark Lake (Missouri River), Daphnia and Cyclops
were important food items for fish 6-15 mm long; bottom fauna became main
food item in diet of fish > 20 mm (Swedberg and Walburg 1970). In a
Tennessee reservoir without mollusks, diet switched to fish; all size groups
collected included individuals that had consumed insects (larvae and pupae
of chaoborines and small chironomids) or plankton (Leptodora; Dendy 1946).
Will feed at all hours of the day (Priegel 1967b).
Growth: In an
Alabama reservoir, estimated total lengths (mm) per age group were 81 (age
1), 145 (age 2), 198 (age 3), 241 (age 4), 295 (age 5), 348 (age 6), 406
(age 7), 475 (age 8), 551 (age 9), 607 (age 10), 648 (age 11), 676 (age 12),
and 696 mm (age 13; Wrenn 1969). Average total lengths of fish from the Salt
River, Missouri (lower station): 119 mm at the end of year 1, and 203, 257,
and 279 mm at the end of years 2-4, respectively; averages from the Salt
River (middle station): 130 mm at the end of year 1, and 218, 267, and 320
mm at the end of years 2-4, respectively (Purkett 1958). In a study
of sexual dimorphism in Alabama populations, females were significantly
larger and had significantly higher growth rates than males. Males and
females had similar growth rates from 0-4 years of age, but showed
significantly different growth rates across subsequent ages; females grew
significantly faster through adulthood (Rypel 2007).
Phylogeny and morphologically similar fishes:
Aplodinotus grunniens
is the only North American freshwater representative of Family Sciaenidae
(Barney 1926).
Host Records:
Reported from Texas
populations: Trematoda: Homalometron armatum; Nemata: Camallanus
oxycephalus, Contracaecum, Rhabdochona decatrurensis,
Spinitectus gracilis; Copepoda: Argulus flavescens, Ergasilus
arthrosis (Mayberry et al. 2000)
Commercial or Environmental Importance
In Texas, this species is
commonly referred to as the gaspergou, or simply “gou”. The otolith (inner
ear bone) and pharyngeal teeth were regarded as good luck pieces by Native
Americans; even today, otoliths are prized as jewelry pieces and charms, in
some regions (Knapp 1953).
[Additional literature
noting collection of this species from Texas locations includes, but is not
limited to the following: Baughman (1946); Robinson (1959); Uyeno and
Miller (1962); Swift (1968); Kasper and McClure (1976); Rose and Echelle
(1981); Matthews et al. (1985); Kleinsasser and Linam (1987); Linam and
Kleinsasser (1987); Linam et al. (1994); Li and Gelwick (2005).]
References
Barney, R.L. 1926. The distribution of the fresh-water sheepshead,
Aplodinotus grunniens Rafinesque, in respect to the glacial history of
North America. Ecology 7(3):351-364.
Baughman, J.L. 1946. An interesting association of fishes. Copeia
1946(4):263.
Cook, F.A. 1959. Freshwater Fishes in Mississippi. Mississippi Game and
Fish Commission, Jackson. 239 pp.
Daiber, F.C. 1953. Notes on the spawning population of the freshwater drum (Aplodinotus
grunniens Rafinesque) in western Lake Erie. American Midland Naturalist.
50:159-171.
Dendy J.S. 1946. Food of several species of fish, Norris Reservoir,
Tennessee. Journal of Tennessee Academy of Science 21:105-127.
Edwards, R.J., and S. Contreras-Balderas. 1991. Historical changes in the
ichthyofauna of the lower Rio Grande (Rio Bravo del Norte), Texas and
Mexico. The Southwestern Naturalist 36(2):201-212.
Fremling, C.R. 1980. Aplodinotus grunniens (Rafinesque), Freshwater
drum. pp. 756 in D. S. Lee, et al. Atlas of North American
Freshwater Fishes. N. C. State Mus. Nat. Hist., Raliegh, i-r+854 pp.
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Gido, K.B., and W.J. Matthews. 2000. Dynamics of the Offshore fish
assemblage in a southwestern reservoir (Lake Texoma, Oklahoma-Texas). Copeia
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biological integrity of water resources using fish communities. CRC Press,
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Hay, O.P. 1883. On a collection of fishes from the lower Mississippi valley.
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collected in the vicinity of Greenwood, Mississippi, with descriptions of
three new species. Bull. U. S. Bur. Fish. 43(2):105-136
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M.S. Thesis. Texas A&M University, College Station. 80 pp.
Li, R.Y., and F.P. Gelwick. 2005. The relationship of environmental factors
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Linam, G.W., and L.J. Kleinsasser. 1987. Fisheries use attainability study
for Cow Bayou (Segment 0511). River Studies Report No. 5. Resource
Protection Division. Texas Parks and Wildlife Department, Austin. 12 pp.
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. 13 pp.
Matthews, W.J. 1984. Influence of turbid inflows on vertical distribution of
larval shad and freshwater drum. Transactions of the American Fisheries
Society 113:192-198.
Matthews, W.J., L.G. Hill, and S.M. Schellhass. 1985. Distribuiton of
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stratification. Trans. Amer. Fish. Soc. 114:84-91.
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Pflieger, W.L. 1997. The Fishes of Missouri. Missouri Department of
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