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	Erimyzon oblongus   creek chubsucker     Type Locality New York (Mitchill 1815).   Etymology/Derivation of Scientific Name Erimyzon, Greek, 
	meaning “to suck”; oblongus, Latin, meaning “oblong” (Pflieger 1975).   Synonymy Cyprinus oblongus 
	Mitchell1815:459 Erimyzon oblongus 
	claviformis Cook 1959:85.   Characters Maximum size: The 
	maximum size reported length is 419mm (16.5 in) TL for the larger Atlantic 
	Slope subspecies (Carlander 1969). The Mississippi River and Gulf Slope 
	subspecies is smaller with a maximum reported size of 376mm (14.8 in) TL (Boschung 
	and Mayden 2004); however most adult fish are smaller (Ross 2001). 
	  Coloration: Color 
	pattern (except in young with two dark stripes) consists of narrow vertical 
	bars (Hubbs et al. 1991). The back and upper sides are bluish green to 
	brown, becoming more yellow or gold on the sides. The undersides are white 
	to yellow. Scale margins are dark giving the upper sides a cross-hatched 
	appearance. There are five to eight dark blotches on the sides, which are 
	connected by dorsal saddles. The blotches vary from being very distinct 
	vertical bars (especially in young fish) to indistinct or coalesced into a 
	lateral band (in adults). Paired and median fins are yellow orange to gray, 
	and median fins tend to be darker then paired fins. Young fish have a broad 
	black lateral stripe with a yellow stripe above it that runs from the snout 
	to the tip of the caudal fin base. Breeding males are dark brown above, 
	pink-yellow, below, with orange paired fins and yellow median fins (Ross 
	2001).   Counts: 56-76 
	pharyngeal teeth (Eastman 1977); 39-43 (usually 39-41) longitudinal scale 
	rows; 4-18 dorsal fin rays (Hubbs et al. 1991); 7 anal rays; 13-16 pectoral 
	rays; 9 (8-9) pelvic rays (Ross 2001).   Body shape: 
	Cylindrical (Ross 2001); eye smaller (eye length contained more then two 
	times snout length; Hubbs et al. 1991).   Mouth position: 
	Subterminal and oblique (Hubbs et al. 1991).   External morphology: 
	Air bladder with two chambers; dorsal fin base less than one-fourth standard 
	length; lateral line absent (Hubbs et al. 1991). Breeding males have three 
	large tubercles on each side of head and a bilobed anal fin (Ross 2001).   Distribution (Native and Introduced) U.S. distribution: 
	Atlantic slope streams from Maine to Altamaha drainage of Georgia; Gulf 
	slope streams east to Escambia River drainage, Alabama (single population) 
	and west to San Jacinto system Texas. Mississippi Valley in Louisiana, 
	Arkansas, southeast Oklahoma, upland Missouri, Mississippi, west Tennessee, 
	West Kentucky, south Great Lakes drainage in southern tributaries to lakes 
	Michigan, Erie, and Ontario (Wall and Gilbert 1980).  
	  Texas distribution: 
	Occurs in eastern Texas streams from the Red River southward to the San 
	Jacinto Drainage; an early record exists from the Devils River (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 Unites States are currently stable (Warren et al. 2000). Hubbs et 
	al. (1991) listed Erimyzon oblongus as a species of special concern, 
	in Texas.   Habitat Associations Macrohabitat: Occupies 
	small rivers and creeks often highly vegetated (Wall and Gilbert 1980), also 
	less often in ponds (Wagner and Cooper 1963). 
	  Mesohabitat: Wide 
	variety of gradients, bottom types, and vegetation depending somewhat on age 
	and stage of reproductive cycle. Seldom if ever occupies impoundments or 
	springs, but may be taken in spring fed creeks. Young typically in head 
	water rivulets. Adults usually not taken in large series. Populations 
	apparently declining in streams subject to siltation (Wall and Gilbert 
	1980).    Biology Spawning season: March 
	to May, when the water temperature reaches about 17 degrees C (Richardson 
	1913; Breder and Rosen 1966; Boschung and Mayden 2004). Carnes (1958) notes 
	the eastern subspecies spawns at water temperature of 11 degrees C, with 
	most activity at night. The western subspecies spawns at water temperatures 
	of 12-24 degrees C, spawning in the afternoon (Curry and Spacie 1984; Page 
	and Johnston 1990).   Spawning habitat: 
	Usually in small creeks, also in ponds or lakes that lack tributary streams 
	(Carnes 1958). In Indiana, small cleared depressions on the sand bottom of 
	pools just above riffles (Curry and Spacie 1984). Lithopelagophils; 
	rock and gravel spawners with benthic larvae that hide beneath stones 
	(Hankinson 1920; Page and Johnston 1990; Simon 1999).   Reproductive strategy: 
	Males guard spawning location (Curry and Spacie 1984). Hankinson (1920) 
	observed stone pulling by males and apparent acts of spawning. Prior to 
	spawning males defend territories in moderately swift water over beds of 
	gravel or near pits constructed by stonerollers or creek chubs. Males 
	apparently do not initiate the digging of nest pits, but will modify 
	existing pits by pushing stones around with their snouts. Females congregate 
	upstream of males in quiet water, periodically drifting tail first into male 
	territories. Once in a male’s territory, the female digs in the gravel with 
	her snout, apparently signaling to the male that she is ready to spawn. In 
	contrast to most species of suckers, pair spawning is much more common than 
	group spawning, perhaps due to the shallowness of the usual spawning 
	habitat. Actual spawning lasts three to five seconds as the male presses 
	against female. Both release gametes while quivering and stirring the 
	substratum with their caudal and anal fins (Page and Johnson 1990).    Fecundity: Fertilized 
	eggs of the eastern subspecies E. o. oblongus are demersal and 
	semiadhesive, with an average diameter of 1.8 mm; color varies from light to 
	deep golden yellow and yolk occupies most of egg; no oil drops in the yolk 
	mass; hatching occurs in 96 hours at a temperature of 20 degrees C (Kay et 
	al. 1994). Egg production varies from 8,694-83,013 in fish 111-1110 g 
	(Carnes 1958). Regardless of high fecundity this species is not found in 
	high numbers (Boschung and Mayden 2004).   Age at maturation:  
	  Migration: An upstream 
	migration often precedes spawning (Breder and Rosen 1966).   Growth and population 
	structure: For the western subspecies E. o. claviformis TL 
	averages 48-51 mm after one year and 104-107mm at end of the second year 
	(Lewis and Elder 1953; Carlander 1969). There is no sexual dimorphism in 
	size (Ross 2001). Newly hatched protolarvae are 4.8-6.6 mm TL (Kay et al. 
	1994).   Longevity: Females may 
	live for 6 or 7 years, though males only live for 5 years (Carnes 1958; 
	Wagner and Cooper 1963; Carlander 1969).   Food habits: 
	Invertivore; major food items include copepods, cladocerans, chironomid 
	larvae and other bottom organisms (Goldstein and Simon 1999). Diet includes 
	organic detritus (including plant fragments), algae, diatoms, midge larvae 
	(Diptera), small clams, and zooplankton (primarily copepods). Food habits 
	are similar to E. sucetta, the lake chubsucker (Flemmer and Woolcott 
	1966; Gatz 1979; Sheldon and Meffe 1993). Feeding begins 7.4 days after 
	hatching at a length of 7.7 mm TL (Kay et al. 1994).   Phylogeny and morphologically similar fishes: 
	 Two subspecies recognized, 
	E. o. claviformis, which occurs in the Gulf of Mexico and Mississippi 
	River Basins, and the Atlantic Slope subspecies E. o. oblongus (Wall 
	and Gilbert 1980). E. oblongus is most closely related to E. 
	sucetta, and two species are known to hybridize (Hanley 1977). The genus
	Erimyzon is most closely related to Minytrema, and both genera 
	are placed within the tribe Moxostomatini (Smith 1992).    Erimyzon oblongus is 
	most similar to the lake chubsucker. It differs from the lake chubsucker in 
	its higher lateral scale count (usually 39-40 or more versus 37 or fewer) 
	and its lower dorsal ray count (10-11 versus 11-12). (Gilbert and Wall 
	1985). Compared to lake chubsuckers, creek chubsuckers have more cylindrical 
	bodies, lighter colored fins and less deeply emarginated caudal fins (Ross 
	2001).   Host Records: Cestoda: Monobothrium sp. 
	Biacetabulum sp. (Arnold et. al 1967); Acanthocephala: 
	Neoechinorhynchus prolixoides, Crustacea: Lernaea cyprinacea 
	(Hoffman 1967).   Commercial or Environmental Importance     References 
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	Fisheries, Conservation. 25(10):7-29.   |