Alabama hogsucker

Alabama hogsucker
Scientific classification
Kingdom: Animalia
Phylum: Chordata
Class: Actinopterygii
Order: Cypriniformes
Family: Catostomidae
Genus: Hypentelium
Species: H. etowanum
Binomial name
Hypentelium etowanum
(D. S. Jordan, 1877)

Alabama hogsucker (Hypentelium etowanum), commonly known as the Alabama Hog Sucker, is a species of sucker fish belonging to the Catostomidae family. The Alabama Hog Sucker, as it is commonly known, is distributed in the Chattahoochee River and Mobile Bay drainages throughout Georgia, Alabama, Mississippi, and southeast Tennessee. Hypentelium etowanum inhabits rocky riffle areas, run, and pools of clear freshwater. They can live in small creeks up to large rivers. Hypentelium etowanum can feed on bottom dwelling creatures by turning over rocks with their bony head and long snout. Diet of collected Hypentelium etowanum indicate that 90.6% of the contents in their stomachs were Diptera, with Chironomidae larvae making up 88.8% of all food items.[1] It is a benthic dweller and feeds off the bottom by using its specialized sucker mouth. Sexual maturity occurs as early as 110 mm, and developed tubercules suggests spawning occurs from March until May. A length-frequency distribution suggests a life span of at least 5 years. Its spawning habitat is over gravel in pools and riffles. Hypentelium etowanum is not on any threatened or endangered list; however it is still adversely influenced by factors such as construction of roads or dams, pollution, oversiltation, and agriculture. National and State Parks and Forests are included within the range of Hypentelium etowanum which will preserve the habitat. While Hypentelium is not considered a game fish, its ecological role on streams is important in the cycling of nutrients. Hogsuckers are a good indicator species of a waterway's health, as they are intolerant of polluted and dirty water conditions.

Taxonomy

There are three species within Hypentelium: H. roanokense, H. nigricans, and H. etowanum. The separation between H. roanokense, which inhabits the Atlantic slope and the rest of Hypentelium is pattern that is replicated within other clades of fishes. However there is a historical connection of the Tennessee River with the Mobile Basin[2][3] which indicates a closer sister relationship among H. nigricans and H. etowanum.[4]

Geographic distribution

Hypentelium etowanum is common in streams throughout the Chattahoochee River and Mobile Bay drainages throughout Georgia, Alabama, Mississippi, and southeast Tennessee. Only headwaters and tributaries of the Mobile Basin are located in southeast Tennessee, making the range of Hypentelium etowanum very narrow in Tennessee. These headwaters include the Conasauga River and its tributaries in Bradley and Polk counties, Tennessee.

Ecology

Hypentelium etowanum prefers a high-gradient stream with rapidly flowing, clear, freshwater. It is characterized by its broad bulky head, slender cylindrical bodies, dark saddles across the back, and bright orange pectoral, pelvic, and anal fins. Hypentelium etowanum have distinct fleshy and papillose lips with a protrusible sucker mouth. It lives on the bottom of fast moving streams and its unique mouth allows it to feed on the benthic substrate. Feeding occurs at or near the stream floor. They scrape algae from rocks, turn over stones for aquatic insects, and suck up decaying plant material. Other foods include snails, clams, worms, mussels, fish eggs, and crustaceans. O’Kelley completed a one year study on Hypentelium etowanum, and when the stomach contents were examined, found that the diet of collected H. etowanum consisted of 90.6% Diptera, with Chrinomidae larvae making up 88.8% of all food items.[1] The weight of stomach contents was not uniform during O’Kelley’s study and there was a feeding peak in April. The greatest variety of food items and the highest mean weight of the stomach contents were also in April.[1]

Life History

Hypentelium etowanum grow rapidly in April, as indicated by length and weight increases at approximately 12, 24, and 36 months of age. The increased feeding during spring coincides with increased energetic requirements associated with spawning. Its spawning habitat is over gravel in pools and riffles of freshwater streams. Typically when spawning, one female is flanked on each side by two males. Developed tubercles suggest spawning occurs from March until May, and that sexual maturity occurs at around three years of age or at a length around 110 mm. There is no parental care invested in the eggs, which typically hatch 10 days after fertilization. A length-frequency distribution indicates that a life span of five years or more is typical among Hypentelium etowanum. O’Kelley also found that the smallest female he collected with mature ova was 24 months, and the smallest male with mature testes was 22 months in age.[1] The smallest specimen collected was a female 34.58 mm SL and 0.942 g TW and the largest specimen was a female 190 mm SL and 132 g TW.[1]

Conservation and management

Hypentelium etowanum is not on any current threatened or endangered list. Hypentelium etowanum is abundant where it is found in its native range. Since Hypentelium etowanum is not endangered or threatened, there are currently no management plans to control or monitor this fish.

References

  1. 1 2 3 4 5 O’Kelley, C.T., and S.L. Powers. 2007. Life-history aspects of Hypentelium etowanum (Alabama Hog Sucker) (Actinopterygii:Catostomidae) in northern Georgia. Southeastern Naturalist 6: 479-490.
  2. Starnes, W.C., and D.A. Etnier. 1986. Drainage evolution and fish biogeography of the Tennessee and Cumberland Rivers drainage realm. The zoogeography of North American frewshwater fishes. 325-361.
  3. Mayden, R.L. 1988. Vicariance biogeography, parsimony, and evolution in North-American fresh-water fishes. Systematic Zoology 37: 329-355.
  4. Berendzen, P.B, A.M. Simmons, and R.M. Wood. 2003. Phylogeography of the northern hogsucker, Hypentelium nigricans (Teloeosti: Cypriniformes): genetic evidence for the existence of the ancient Teays River. Journal of Biogeography 30: 1139-1152.
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