Amia calva
bowfin
Type Locality
Charleston, South Carolina
(Linnaeus 1766).
Etymology/Derivation of Scientific Name
Amia, an ancient Greek
name for a type of fish, probably the bonito (Sarda sarda); calva,
Latin, meaning “smooth” (Wallus et al. 1990).
Synonymy
Amia calva Linnaeus
1766:500; Hildebrand and Towers 1928:113; Cook 1959:64 (Ross 2001).
Characters
Maximum size: 1090 mm,
(43 in)
TL (Page and Burr 1991).
Coloration: Dark
greenish above, lighter below, with dark reticulations on body and some
fins; males with black spot on the dorsal part of the caudal
base (Miller and Robison 2004).
Counts: Lateral line
scale count 62-70; 42-53 dorsal fin soft rays; 9-12 anal fin soft rays (Mansueti and
Hardy 1967); 16-18 pectoral fin soft rays; 9 pelvic fin soft rays (Heufelder 1982).
Body shape: Long,
robust body; head conical (Mansueti and Hardy 1967).
Mouth position:
Terminal (Goldstein and Simon 1999).
Morphology:
Large bony gular plate (Goldstein and Simon
1999); single, long, dorsal fin; rounded pectoral, pelvic, and
caudal fins (Scott and Crossman 1973); heterocercal tail (Heufelder 1982);
scales cycloid; anterior nostrils at end of short barbels (Mansueti and
Hardy 1967). Gut rudimentary spiral valve (Goldstein and Simon 1999) which can function
as lung (Wallus et al. 1990); jaws with numerous strong, conical teeth
(Mansueti and Hardy 1967; Wallus et al. 1990).
Distribution (Native and Introduced)
U.S. distribution:
Occur from the Great Lakes and drainages southward to central Texas and
eastward throughout Florida; introduced populations now occur in Appalachian
streams (Hubbs et al. 1991).
Texas distribution:
Found in the Red, San Jacinto, and Sabine river systems and in the
downstream reaches of the Brazos and Colorado basins (Hubbs et al. 1991).
Warren et al. (2000) listed the following drainage units for distribution of
Amia calva 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.
[Additional literature
noting collection of this species from Texas locations includes, but is not
limited to the following: Bettoli et al. (1993); Linam et al. (1994);
Gelwick and Li (2002); Hubbs (2002).]
Abundance/Conservation status (Federal, State,
Non-government organizations):
Currently stable (Warren et
al. 2000).
Habitat Associations
Macrohabitat: Sluggish
lowland waters (Burgess and Gilbert 1980).
Mesohabitat: Clear
waters, often abundantly vegetated (Burgess and Gilbert 1980). According to
Cahn (1927) species commonly found in weed beds just over the edge of sand
bars. Fish are
able to survive in poorly-oxygenated habitat; when the area no longer holds
water, fish may burrow in the mud and reemerge when water has returned
(Neill 1950; Green 1966). Able to gulp air at water surface (Burgess and
Gilbert 1980; Katula and Page 1986) and tolerates high temperatures (Burgess
and Gilbert 1980).
Biology
Spawning season: In
the spring (Hildebrand and Towers 1928; Burgess and Gilbert 1980) or early
summer (Breder and Rosen 1966); late-March to June (Wallus et al. 1990); at
water temperatures between 16-19°C, (61-66°F) (Mansueti and Hardy 1967; Heufelder 1982;
Wallus et al. 1990). In southeastern Louisiana, spawning occurred in late
February and early March (Davis 2006).
Spawning location:
Occurs in vegetated areas in shallow water (Breder
and Rosen 1966; Burgess and Gilbert 1980); also under stumps, logs, and
bushes (Mansueti and Hardy 1967; Wallus et al. 1990).
Katula and Page (1998) observed a nest
located near the shore of a heavily vegetated pond in shallow water; nest had been constructed on flooded terrestrial grasses; the shoots
of grasses had been broken off during nest construction, and the bottom of
the nest was mud with exposed roots. Phytophils – plant material nesters
that have adhesive eggs and free embryos that hang on plants by cement
glands (Breder and Rosen 1966; Balon 1975; Simon 1999).
Reproductive strategy:
Guarders; nest spawners (Simon 1999). Spawning usually occurs at night,
occasionally by day, lasting 1-3 hours (Mansueti and Hardy 1967). Males
build circular nests (Burgess and Gilbert 1980), guard eggs during
incubation, and protect schooling young after hatching (Cahn 1927;
Hildebrand and Towers 1928; Burgess and Gilbert 1980; Wallus et al. 1990).
By fanning the caudal and pectoral fins, and using the snout to break off
plant shoots, the male clears a large circular nest area 460-760 mm (18-30
in) in diameter,
and 100-200 mm (4-8 in) deep which may have a tunnel-like entrance at one side through
dense vegetation. After a female appears, the pair circle about touching
intermittently, finally positioning themselves side by side where the female
then lays the eggs and the male fertilizes; this process may occur up to 6
times. A male may spawn with successive females, and a single female may
spawn in multiple nests. Male guards nest aggressively, until the young are
at least 102 mm (4 in) long. Young leave the nest in a group, while the male slowly
circles them, in an effort to prevent any from becoming separated (Breder
and Rosen 1966).
Fecundity: In
Louisiana, mean fecundity was about 23,000 eggs, with a range of
1,900-72,500 eggs; mean number of eggs per gram of body weight was 15
eggs/gram of body weight; mean egg diameter was 2.0 mm (.08 in) from December to
April; females that did not spawn retained and reabsorbed eggs (Davis 2006).
23,600 eggs produced by female measuring 480 mm (19 in); 64,000 eggs reported
from ovaries of a 530 mm (21 in) fish (Vessel and Eddy 1941). In Missouri,
relationship between body length and number of eggs was variable – mature
females (470-843 mm, 18.5-33.2 in TL) averaged 21,332 eggs per fish; an 843 mm
(33.2) TL female
had 98,737 eggs (Wallus et al. 1990). Eggs slightly elliptical in shape; hatching in 180 hours (Breder and Rosen 1966).
Katula and Page (1998) reported collection of eggs from a nest, which were
black in color, and measured 2 mm (.08 in) in diameter. Eggs creamy-yellow when first
laid, darkening quickly; white to yellowish brown animal pole and charcoal
gray to dark, grayish brown yolk; eggs darken with age, and vary in color
with locality (Mansueti and Hardy 1967; Wallus et al. 1990). According to
Davis (2006), spawning behavior is completed between 16 and 25 days; this
based on the following information from earlier studies: 1-6 day time frame
for nest construction and egg deposition, 8-10 days for hatching, and 7-9
days for yolk-sac absorption while larvae is attached to vegetation.
Age at maturation: In
southeastern Louisiana, most fish were mature by age 2 (Davis 2006). In
Canada, males and females may mature from age 3-5 (Wallus et al. 1990).
Minimum TL at maturation is reported at about 380 mm, 15 in (Trautman 1957; Wallus et
al. 1990).
Migration: During high
water, bowfin move into floodplain habitats and return to the river
channel as floodplains start to become dry (Davis 2006; Greenbank 1956).
Migration during spawning season has been reported (Mansueti and Hardy 1967; Wallus
et al.1990).
Longevity: 10 years
reported from Louisiana; females were older than males (Davis 2006). Fish in
captivity may live up to 30 years (Carlander 1969).
Food habits: First and
second level trophic classifications: carnivore and whole body,
respectively; trophic mode: ambush (in conjunction with protective
resemblance); feeding behavior: clumsy predatory opportunist, generalist,
nocturnal; main food items include fishes, crayfish, and frogs (Burgess and
Gilbert 1980; Goldstein and Simon 1999). In southeastern Missouri, fish
(especially gizzard shad, but including golden shiner, bullheads, and
sunfish) represented about 65% of the adult diet, with crayfish (important
diet item from March – June) constituting the majority of what remained;
young bowfin (<102 mm, 4 in) consumed mainly water fleas and other microscopic
animals (Plieger 1975). Pearse (1918) examined Wisconsin specimens and
reported food items of fish remains (90.1%) and crayfish remains (9.4%).
Cahn (1927) reported that the diets of southern Wisconsin populations
consisted of fish (including small specimens of largemouth and smallmouth
bass as along with yellow perch) and crayfish (dominant item
in late summer and fall). In the Kissimmee River, Florida, species fed on
herpetofauna (Jordan and Arrington 2001).
Growth and population
structure: Early growth is rapid (Wallus et al. 1990). In
southeast Missouri, fish are about 178-229 mm (7-9 in) long by the end of the
first year, and attain a length of about 508 mm (20 in) when 5 or 6 years old
(Pflieger 1975). In Louisiana, sex ratio of
females to males was 2.3:1; females were longer and heavier than males
(Davis 2006).
Phylogeny and morphologically similar fishes:
Only living representative of
Amiiformes (Burgess and Gilbert 1980).
Host Records:
Numerous parasites listed by
Hoffman (1967): Trematoda, Cestoda, Nematoda, Acanthocephala, Leech,
Crustacea, Linguatula.
Commercial or Environmental Importance:
Status of species as “living
fossil”, ease of maintenance, and interesting physiological and behavioral
attributes has lead to its common use as a laboratory test animal (Burgess
and Gilbert 1980). Due to its predatory
nature, species has been considered a valuable tool in managing sport fish
populations (Wallus et al. 1990). In
Louisiana, eggs are marketed as less expensive caviar under the name "Choupiquet
Royale" (Arceneaux 1992). Nests constructed
by bowfin may be used for spawning by the golden shiner (Katula and Page 1998).
References
Arceneaux, H. 1992. Mining golden eggs from choupique. La. Conserv.
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Balon, E.K. 1975. Reproductive guilds of fishes: a proposal and definition.
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