|   Fundulus grandis  Gulf killifish     Type Locality Indianola, Texas (Baird and 
	Girard 1853).   Etymology/Derivation of Scientific Name Fundulus – Latin 
	diminutive of fundus, “bottom”; grandis – Latin "big, large; 
	full grown” (Boschung and Mayden 2004).   Synonymy     Characters Maximum size: 145 mm 
	SL (Relyea 1983). 
	  Coloration: Predorsal 
	stripe may be present but fades with age (Relyea 1983). Predorsal spot 
	absent or not reaching occiput; no dark subocular bar; body mottled, barred 
	or irregularly spotted (Hubbs et al 1991, 2008). Base color is dull greenish 
	above shading to lemon yellow below; 12-19 faint stripes on the sides; anal 
	and lower half of caudal may be yellow or the anal, dorsal and caudal may be 
	dark with white splotches at base; first two may be edged with yellow, 
	caudal may be edged with white; ventrals are yellow and the pectorals pale; 
	in some males, dorsal and caudal are flecked with silver and the anal is 
	pale; coloration in males much more vivid with silver flecking and striping 
	noticeable; larger females may appear olive to dull olive yellow below 
	(Simpson and Gunter 1956).   Counts: More than 15 
	scale rows from pelvic fin origin to isthmus; 31-39 longitudinal scale rows 
	(Hubbs et al 1991, 2008); 17-20 scales around caudal peduncle; 9-12 gill 
	rakers, 10-12 dorsal rays; 9-11 anal rays; 16-18 pectoral rays; 6 pelvic 
	rays (Ross 2001); 5 pairs of mandibular pores (Stevenson 1976). 
	  Body shape: Dorsal fin 
	originating anterior to anal fin origin; eye goes fewer than 1.5 times in 
	snout (Hubbs et al. 1991, 2008). Large, stout-bodied with blunt head; 
	relative body depth increases with fish size; head length goes into SL 
	2.8-3.2 times (Ross 2001).  
	  Mouth position: Nearly 
	terminal, lower jaw is slightly projecting (Ross 2001). 
	  External morphology: 
	Gill slit 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, 2008); anal fin rounded, its base more than half length 
	of its longest rays (Stevenson 1976).   Distribution (Native and Introduced) U.S. distribution: 
	Primarily found in coastal waters and their tributaries from Florida to 
	Laguna de Tampamachoco, Veracruz, Mexico (Hubbs et al. 2008). Found in 
	drainages along the coast from the northern border of Florida to the Gulf 
	Coast of Texas. (Burgess 1980). Fundulus grandis is native to the 
	following western Gulf of Mexico Slope drainages (North America): Nueces, 
	San Antonio Bay, Colorado, Brazos, Galveston Bay, Sabine Lake, and Calcasieu 
	(Conner and Suttkus 1986); in the Rio Grande Region, species is native to 
	the lower Rio Grande, San Fernando and Soto la Marina drainages (Smith and 
	Miller 1986); and in Central Mexico, species 
	is native to the Panuco Drainage (Miller and Smith 1986). 
	  Texas distribution: 
	Occurs in large numbers in Brazos River, Hill and Bosque Counties, over 400 
	km from the Gulf Coast (Hillis et al. 1980). Often introduced as a “bait 
	minnow” and occurs widely in the Brazos, Rio Grande and Pecos Basins (Hubbs 
	et al. 1991, 2008).    Abundance/Conservation status (Federal, State, NGO) Currently Stable in the 
	southern United States (Warren et al. 2000). 
	Inhabits most sections (or at one time inhabited most portions) of the Rio 
	Grande (Texas and Mexico) from the area that is now Falcon Reservoir to the 
	mouth; one of several species numerically dominating upstream fauna of this 
	area, and apparently increasing in abundance in some portions of the Rio 
	Grande River (Edwards and Contreras-Balderas 1991).   Habitat Associations Macrohabitat: Common 
	along bay shores and tidal marshes in wide range of salinities (Burgess 
	1980). Found in the following habitats (western Gulf Slope): estuarine, 
	lowland, upland, coastal marshes/lagoons, rivers and streams (Conner and 
	Suttkus 1986). 
	  Mesohabitat: From 
	freshwater (Tabb and Manning 1961) to tidal pools of 76 ppt. salinity 
	(Simpson and Gunter 1956). Most abundant on vegetated areas (inner 
	Spartina alterniflora or S. patens marsh) of upper Galveston Bay 
	and East Bay, Texas; one of several species numerically dominating fish 
	assemblage in upper Galveston Bay in the spring and fall (Rozas and 
	Zimmerman 2000). In Texas, Gunter (1950) reported species preferred open and 
	partly salty waters to inland ponds. Hillis et al. (1980) list records of 
	collections from inland locales in Texas which show specimens taken 
	primarily from clear, shallow riffles; at one locality most abundant in 
	quiet, shallow pools along the shore where Fundulus grandis was the 
	only species collected. In a study of Florida individuals, species lived a 
	maximum period of 1 month in freshwater after a gradual transfer from 
	brackish water (Griffith 1974).   Biology Spawning season: In 
	Texas, from March to October (Gunter 1950; Simpson and Gunter 1956).   Spawning habitat: Eggs 
	are deposited in shallow water in dense beds of marsh grass (Spartina; 
	Greeley and MacGregor 1983).   Spawning Behavior: 
	Male forces female into a cove, clump of debris, or among oysters, clasping 
	her with dorsal and anal fins (Boschung and Mayden 2004).   Fecundity: Estimated 
	on the basis of the condition of ovaries during the semilunar spawning peak: 
	from 872 to 12,858 eggs annually, or an average of about 400 per semilunar 
	cycle and about 80 eggs daily over a 5-day period. Fertilized eggs are about 
	2 mm in diameter, demersal, and adherent (Greeley et al. 1988). Eggs 
	deposited during periods of maximum high tides (spring tides), develop while 
	they are exposed to humid air; eggs hatch when inundated on the next high 
	tide, usually in about 13-15 days (Greeley and MacGregor 1983). Foster 
	(1967) reported egg size ranging 2.6-2.9 mm in diameter. In Texas, Simpson 
	and Gunter (1956) collected yellow eggs, 2.0 mm diameter from females in 
	October. Perschbacher et al. (1990) compared survival and growth of the 
	early stages of gulf killifish in various salinities and found salinity 
	ranges of 0-40‰ to be suitable for incubation.   Age at maturation: 
	   Migration:    Growth and Population 
	structure: Females reach larger sizes than males. Ripe females taken in 
	April and May were 65-91 mm long. Two specimens, 21 and 21 mm long, 
	evidently young-of-year were taken in July (Gunter 1950). Perschbacher et 
	al. (1990) compared survival and growth of the early stages of gulf 
	killifish in various salinities and found salinity ranges of 5-40‰ to be 
	suitable for fry growth and survival.   Longevity:    Food habits: 
	Omnivorous; algae and vascular plants are consumed; animal prey include 
	grass shrimp (Palaemonetes), microcrustaceans (copepods), mosquito 
	(Dipteran) larvae and pupae, bivalve mollusks, and small fishes (Simpson and 
	Gunter 1956; Springer and Woodburn 1960; Harrington and Harrington 1961).   Phylogeny and morphologically similar fishes Subgenus Fundulus 
	(Wiley 1986). Blunt head and deep caudal peduncle of large gulf killifish 
	distinctive; however, young individuals could be confused with the golden or 
	bayou topminnow. Gulf killifish differs from the golden topminnow (F. 
	chrysotus) in having the dorsal fin origin over or in front of the anal 
	fin origin, rather than posterior to it; it differs from the bayou killifish 
	(F. pulvereus) in having more gill rakers (9-12 versus 5-7) and in 
	lacking well-defined vertical bars (males) or black spots (females) on the 
	sides (Ross 2001).   Host Records Trematoda: Ascocotyle 
	angrense, Dactylogyrus stephanus, Gyrodactylus prolongis,
	Parascocotyle diminuta (larval form). Acanthocephala: 
	Octospinieroides chandleri (Hoffman 1967). Several species of Cestoda, 
	Trematoda, Nemata and Acanthocephala (Mayberry et al 2000).   Commercial or Environmental Importance Popular as bait fish for 
	coastal fishing and are sold locally as cigar or bull minnows (Ross 2001). 
	Gulf killifish are important predators of mosquito larvae and pupae 
	(Harrington and Harrington 1961).   [Additional literature 
	noting collection of this species from Texas locations includes, but is not 
	limited to the following: Redfish Bay (Port Aransas; Moore 1976); Pecos 
	River (Rhodes and Hubbs 1992); Gelwick et al. (2001).]   References  
	Baird, S. F., and C. Girard. 1853. Description of new species of fishes, 
	collected by Captains R. B. Marcy, and Geo. B. M’Clellum, in Arkansas. Proc. 
	Acad. Nat. Sci. Phil. 6(7):387-390. 
	Boschung, H. T. and R. L Mayden. 2004. Fishes of Alabama. Smithsonian Books. 
	Washington, 736 pp. 
	Burgess, G.H. 1980. Fundulus grandis (Baird and Girard) Gulf 
	Killifish. pp 516 in D.S. Lee et al. Atlas of North American 
	Freshwater fishes. N.C. State Mus. Nat. Hist., Raleigh, i-r+854. 
	Conner, J.V., and R.D. Suttkus. 1986. Chapter 12 – Zoogeography of 
	Freshwater Fishes of the Western Gulf Slope. Pp. 413-456 in: Hocutt, 
	C.H., and E.O. Wiley (Eds.). The Zoogeography of North American Freshwater 
	Fishes. John Wiley and Sons, New York, New York. 866 pp. 
	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. 
	Foster, N.R. 1967. Comparative study on the biology of killifishes (Pisces, 
	Cyprinodontidae). Ph.D. dissertation, Cornell University, Ithaca, NY. 
	Gelwick, F.P., S. Akin, D.A. Arrington, and K.O. Winemiller. 2001. Fish 
	assemblage structure in relation to environmental variation in a Texas Gulf 
	Coastal wetland. Estuaries 24(2):285-296. 
	Greeley, M. S., Jr., and R. MacGregor. 1983. Annual and semilunar 
	reproductive cycles of the gulf killifish, Fundulus grandis, on the 
	Alabama Gulf Coast. Copeia 1983(3):711-718. 
	Greeley, M. S., Jr., R. MacGregor III, and K. R. Marion. 1988. Changes in 
	the ovary of the gulf killifish, Fundulus grandis, (Baird and Girard) 
	during seasonal and semilunar spawning cycles. J. Fish. Biol. 33:97-107. 
	Griffith, R.W. 1974. Environment and salinity tolerance in genus Fundulus. 
	Copeia 1974(2):310-331. 
	Gunter, G. 1950. Distributions and abundance of fishes on the Aransas 
	National Wildlife Refuge, with life history noted. Publ. Inst. Mar. Sci., 
	Univ. Tex. 1(2):89-101. 
	Harrington, R. W., Jr. and E. S. Harrington. 1961. Food selection among 
	fishes invading a high subtropical salt marsh: from onset of flooding 
	through the progress of a mosquito brood. Ecology 42(4):646-666. 
	Hillis, L. G., E. Milstead, and S. L. Campbell. 1980. Inland records of 
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	University of California Press. Berkeley, 486 pp. 
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	Journal of Science, Supplement. 43(4):1-56.   Hubbs, C., 
	R.J. Edwards, and G.P. Garrett. 2008. An annotated checklist of the 
	freshwater fishes of Texas, with keys to identification of species. Texas 
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	Bibliography of parasites and vertebrate host in Arizona, New Mexico and 
	Texas (1893-1984). University of Nebraska Harold W. Manter Laboratory of 
	Parasitology Web Server, published on the World-Wide-Web, 100 pp. 
	Miller, R.R., and M.L. Smith. 1986. Chapter 14 – Origin and Jurisdiction of the
	Fishes of Central Mexico. Pp. 487-518 in: Hocutt, C.H., and E.O. 
	Wiley (Eds.). The Zoogeography of North American Freshwater Fishes. John 
	Wiley and Sons, New York, New York. 866 pp. 
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	Mexico. The University of Chicago Press. Chicago, 490 pp. 
	Moore, R.H. 1976. Observations on fishes killed by cold at Port Aransas, 
	Texas, 11-12 January 1973. The Southwestern Naturalist 20(4):461-466. 
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	of the early stages of gulf killifish in various salinities. The Progressive 
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	Fundulus (Pisces: Cyprinodontidae). Bull. Fla. St. Mus., Biol. Sci. 
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	Mississippi, Jackson. 624 pp. 
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	Estuary, Texas (USA). Marine Ecology Progress Series 193:217-239. 
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