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Fundulus kansae
Northern plains killifish
Type Locality
Kansas (Garman 1895).
Etymology/Derivation of Scientific Name
Fundulus, from the
Latin name Fundus, meaning "bottom," the habitat (Pflieger 1997);
kansae refers to the type locality.
Synonymy
Fundulus kansae Garman
1895:103-104.
Plancterus kansae
Hubbs 1926:15.
Fundulus zebrinus
Hubbs et al. 1991:31-32.
Kreiser et al. (2001) and
Kreiser (2001) presented data supporting the recognition of two species of
plains killifish: Fundulus kansae and Fundulus zebrinus.
Characters
Maximum size: 100 mm
TL (Shute and Allen 1980; Page and Burr 1991).
Coloration: Light
brown to tan above grading to yellowish or light below. Series of 12-26 thin
dark vertical bars located along the sides and dorsum (bars narrower and
more numerous in females than in males); fins plain or yellowish in females
and immature individuals, bright yellowish-orange in breeding males (Koster
1957; Pflieger 1997; Miller and Robison 2004).
Counts: 52-64 lateral
scale rows (Hubbs 1926; Koster 1957), small scales with no lateral-line
pores; about 14 dorsal rays; 13-14 anal fin rays (Miller and Robison 2004);
15-18 pectoral fin rays; 6-7 pelvic fin rays; 16-18 caudal fin rays
(Sublette et al. 1990).
Body shape:
Compressed, moderately elongated body with large head, wide mouth, and
projecting lower jaw (Koster 1957).
Mouth position:
Terminal; lower lip large and fleshy (Sublette et al. 1990).
External morphology:
Dorsal fin long and rounded; pectoral and pelvic fins ovate, pectorals much
larger than pelvics; anal fin elongate, sharply angulate; caudal fin
truncate (Sublette et al. 1990). Gill slit not extending dorsal to uppermost
pectoral fin ray. Distance from origin of dorsal fin to end of hypural plate
less than distance from origin of dorsal fin to preopercle or occasionally
about equal to that distance (Hubbs et al 1991). The least width of the
preorbital, the flat bone between the eye and the mouth, is only one-half to
two-thirds as great as the diameter of the eye (Koster 1957). Male has
slight depression in the region of the urogenital papilla; female has an
oviducal sheath surrounding the urogenital region and the anterior edge of
the anal fin (Bonham 1962). Males possess small slender contact organs,
hooked forward, on the anal fin and adjacent portion of the body (Hubbs
1926).
Internal morphology:
Both jaws with villiform bands of teeth, external row enlarged (Sublette et
al. 1990).
Distribution (Native and Introduced)
U.S. distribution:
Native to Mississippi River and Gulf Slope basins from north-central MO to
central WY, and south to TX. Also present, and thought to be introduced, in
upper Missouri River basin, SD, MT, and WY (Page and Burr 1991). Kreiser
(2001) reported collection of species from the Platte, Smoky Hill, Arkansas,
and Canadian Rivers (drainages north of but not including the Red River;
Kreiser et al. 2001).
Texas distribution:
Canadian River (Kreiser 2001).
Abundance/Conservation status (Federal, State, NGO)
Populations in the southern
United States are currently stable (Warren et al. 2000). Species is abundant
throughout the southern Great Plains of the United States (Hubbs et al.
1991).
Habitat Associations
Macrohabitat: Ponds,
streams, rivers (Cross and Moss 1987); found in small, loosely organized
schools composed of fish of the same general size (Bonham 1962; Minckley and
Klaassen 1969b).
Mesohabitat: Cross and
Moss (1987) reported that species inhabits shallow, turbid waters over
sandy-bottom, with slow to moderate current and elevated dissolved solids.
Normally found in shallow (rarely deeper than 15 cm), sandy-bottomed
streams; many localities highly alkaline or saline (Minckley and Klaassen
1969; Shute and Allen 1980). Griffith (1974) reported a high salinity
tolerance of 89% for the species, this in accordance with its occurrence in
inland saline waters; Bonham (1962) provided data showing that the species
is well suited to a saline environment. Fish
observed in pools when water temperature was as high as 35°C. During
periods of inactivity, it often lies buried in the sand with only its head
showing. This behavior may allow the fish protection from the effects of
high temperature by allowing a decrease in metabolism; also, the sand is
considerably cooler than the water (Bonham 1962). Minckley and Klaassen
(1969a) noted that schooling F. kansae, when alarmed, will respond as
a unit in flight or concealment; the latter achieved by burying in the
substrate.
Biology
Spawning season:
Occurs from June – August (Hubbs and Ortenburger 1929; Koster 1948);
spawning observed at water temperature of 27.7°C (Koster 1948).
In Missouri, during the spawning period from early June to early
August, there may be three or more separate periods of spawning activity
during the spawning season. In Salt Creek, Missouri, each spawning period
follows a moderate or heavy rain, which suggests that spawning activity is
stimulated by a sudden freshening of the water or a change in water
temperature (Bonham 1962).
Spawning habitat:
Occurs in small pools over sand and gravel bottom (Koster 1948; Carlander
1969).
Spawning Behavior:
Males do not establish territories but become aggressive toward each other
while spawning and compete vigorously for the attentions of the females;
spawning occurs during a brief pairing of a single male and female (Koster
1948). The eggs are deposited over sand or gravel and rubble in water less
than 10 cm deep; eggs are left unguarded (Koster 1948; Minckley and Kaassen
1969b). Bonham (1962) found eggs are buried
beneath the sand (Bonham 1962).
Fecundity: Bonham
(1962) provided data for a population in Missouri: the average number of
mature eggs in the ovary of the most dominant length group, 35-65 mm TL, was
25 eggs; a 75 mm TL female contained 106 mature eggs; smaller females, 35-40
mm TL, rarely contained over 20 eggs, and some females had only 3-5 mature
eggs in the ovary with approximately the same number of immature eggs;
average number of eggs produced by an individual during the spawning season
was 15.
Age/size at maturation:
In Missouri, fish attained sexual maturity at one year of age, and at a
length of approximately 35 mm TL. In the Smokey Hill River, Kansas, fish
became sexually mature in the 2nd summer of life (smallest mature
female was 41 mm TL); age group II was the
major spawning group, as they were larger and more vigorous (Minckley and
Klaassen 1969b).
Migration:
Growth and Population
structure: In a Missouri population, there appeared to be two age
groups present in May: age group I fish measured 31-45 mm TL, and age group
II fish measured from 52-62 mm TL; in June, there was a new peak in the 8-18
mm TL range which represented recruitment of young-of-the-year (Bonham
1962). In the Smokey Hill River, Kansas, main age classes were I and II,
with young-of-the-year (0) making up a third class in early summer:
young-of-the-year measured about 35 mm TL at the end of their first year,
and reached 50 mm TL by the following summer; maximum observed size of
two-year-old fish was 76 mm TL (Minckley and Klaassen 1969b).
Longevity: Most
individuals do not live past 2nd year (Minckley and Klassen
1969b).
Food habits:
Omnivorous (Shute and Allen 1980). Generalist feeder, in Salt Creek,
Missouri, with bulk of diet composed of insects and other aquatic
invertebrates; fish consumed diatoms and other plant material when
invertebrates are difficult to obtain; when diatoms were few in number, fish
consumed large amounts of sand as they fed on the available layer of diatoms
that grew over the sandy bottom (Bonham 1962).
While adapted for top-feeding, this species will feed on the bottom
in shallow sandy streams, primarily ingesting insect larvae, especially
those of Chironomidae and Ephemeroptera (Minckley and Klaassen 1969b).
Bottom-feeding is achieved when the head is tilted downwards and forced into
the substratum past the eye (referred to as “digging” or “nipping”; Echelle
1971).
Phylogeny and morphologically similar fishes
Fundulus kansae
differs from F. zebrinus (plains killifish) in having smaller scales,
smaller eyes, and a less robust body (Hubbs 1926); F. kansae with
yellow orange fins on large male, and 52-68 lateral scales; F. zebrinus
with bright red fins on large male (Page and Burr 1991), and 41-49 lateral
scales (Hubbs 1926). F. kansae has 12 or more vertical dark bands
marking the sides; these bars will distinguish this species from
live-bearers of similar shape (Koster 1957).
Host Records
Myxosoma funduli Kudo 1918 (Protozoa: Myxosporida) reported from the
South Platte River, Nebraska (Knight et al. 1980). The copepod Lernaea
cyprinacea Linnaeus 1758 reported from the South Platte River, Nebraska
(Adams 1984).
Commercial or Environmental Importance
In Kansas, populations have
decreased or been eliminated in western streams due to highly intermittent
flow resulting from irrigation withdrawals (Cross and Collins 1995).
References
Adams, A.M. Infestation of Fundulus kansae (Garman) (Pisces:
Cyprinodontidae) by the copepod Lernaea cyprinacea Linnaeus, 1758, in
the South Platte River, Nebraska. American Midland Naturalist
112(1):131-137.
Bonham, L.E. 1962. Ecology of a saline spring, Boone's Lick. M.A. Thesis,
Univ. Mo., Columbia. 89 pp.
Carlander, K.D. 1969. Handbook of Freshwater Fishery Biology. Volume 1. Iowa
State University Press, Ames. 752 pp.
Cross, F.B., and R.E. Moss. 1987. Historic changes in fish communities and
aquatic habitats in plains streams of Kansas, pp. 155-165. In:
Matthews, W.J., and D.C. Heins (Eds.), Community and evolutionary ecology of
North American stream fishes. University of Oklahoma Press, Norman. 299 pp.
Cross, F.B., and J.T. Collins. 1995. Fishes in Kansas. University Press of
Kansas, Lawrence. 315 pp.
Echelle, A.A. 1971. Diurnal periodicity of activities in the plains
killifish, Fundulus zebrinus kansae. Proc. Oklahoma Acad. Sci.
51:3-7.
Garman, S. 1895. The cyprinodonts. Mem. Mus. Comp. Zool. 19(1).
Griffith, R.W. 1974. Environment and salinity tolerance in the genus
Fundulus. Copeia 1974(2):319-331.
Hubbs, C., and A.I. Ortenburger. 1929. Further notes on the fishes of
Oklahoma with descriptions of new species of Cyprinidae. Publ. Oklahoma.
Biol. Surv. 1(2):17-43.
Hubbs, C.,
R.J. Edwards, and G.P. Garrett. 1991. An annotated checklist of the
freshwater fishes of Texas, with keys to identification of species. Texas
Journal of Science, Supplement 43(4):1-56.
Hubbs, C. L. 1926. Studies of the fishes of the order Cyprinodontes. VI.
Material for a revision of the American genera and species. Misc. Publ. Mus.
Zool. Univ. Mich. 16:1-86.
Knight,
S.A., J. Janovy, Jr., and W.L. Current. 1980. Myxosoma funduli Kudo
1918 (Protozoa: Myxosporida) in Fundulus kansae (Pisces:
Cyprinodontidae): Annual prevalence and geographic distribution. The Journal
of Parasitology 66(5):806-810.
Koster, W.J. 1948. Notes on the spawning activities and the young stages of
Plancterus kansae (Garman). Copeia 1948(1):25-33.
Koster, W.J.
1957. Guide to the Fishes of New Mexico. University of New Mexico Press,
Albuquerque. 116 pp.
Kreiser, B.R. 2001. Mitochondrial cytochrome b
sequences support recognition of two cryptic species of plains killifish,
Fundulus zebrinus and Fundulus kansae. American Midland
Naturalist 146:199-209.
Miller, R.J., and H.W. Robison. 2004. Fishes of Oklahoma. University of
Oklahoma Press, Norman. 450 pp.
Minckley, C.O., and H.E. Klaassen. 1969. Burying behavior of the plains
killifish, Fundulus kansae. Copeia 1969:200-201.
Minckley, C.O., and H.E. Klaassen. 1969b. Life history of the plains
killifish, Fundulus kansae (Garman), in the Smokey Hill River,
Kansas. Trans. Amer. Fish. Soc. 98:460-465.
Page, L. M., and B. M. Burr. 1991. A Field Guide to Freshwater Fishes of
North America, north of Mexico. Houghton Mifflin Company, Boston, 432 pp.
Pflieger, W.L. 1997. The Fishes of Missouri. Missouri Department of
Conservation, Jefferson City. 372 pp.
Poss, S.G., and R.R. Miller. 1983. Taxonomic status of the plains killifish,
Fundulus zebrinus. Copeia 1983(1):55-67.
Shute, J.R., and A.W. Allen. 1980. Fundulus zebrinus (Jordan and
Gilbert), Plains killifish. pp. 531 in D. S. Lee et al., Atlas of
North American Freshwater Fishes. N. C. State Mus. Nat. Hist., Raleigh,
i-r+854 pp.
Sublette, J.E., M.D. Hatch, and M. Sublette. 1990. The Fishes of New Mexico.
University of New Mexico Press, Albuquerque. 393 pp.
Warren, M.L., Jr., B.M. Burr, S.J. Walsh, H.L. Bart, Jr., R.C. Cashner, D.A.
Etnier, B.J. Freeman, B.R. Kuhajda, R.L. Mayden, H.W. Robison, S.T. Ross,
and W.C. Starnes. 2000. Diversity, Distribution, and Conservation status of
the native freshwater fishes of the southern United States. Fisheries
25(10):7-29.
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