Ameiurus nebulosusBrown catfish(Also: Bullhead; Catfish; Common bullhead; Common catfish)

Ge­o­graphic Range

Brown bull­head are na­tive to fresh­wa­ter habi­tats in Canada and the United States from 25° to 54° north lat­i­tude. They are dis­trib­uted in the At­lantic and Gulf Slope drainages, rang­ing from Nova Sco­tia and New Brunswick to Mo­bile Bay, Al­abama, and in the Great Lakes, Hud­son Bay, and Mis­sis­sippi basins from Que­bec west to south­east Saskatchewan and south to Louisiana. Brown bull­head have been in­tro­duced out­side of this range, in­clud­ing coun­tries of north­ern, west­ern, and east­ern Eu­rope, the Mid­dle East, New Zealand, Chile, and Puerto Rico (U.S.). They have also been in­tro­duced and well es­tab­lished in the west­ern United States and British Co­lum­bia. (Amer­i­can Fish­eries So­ci­ety, 2004; Barnes and Hicks, 2003; Fish­eries and Oceans Canada, 2010; Froese and Pauly, 2010; Page and Burr, 1991)

Habi­tat

Brown bull­head are found in pools and slower-mov­ing runs of creeks and rivers, reser­voirs, ponds, and lakes. They are tol­er­ant of a wide range of en­vi­ron­men­tal con­di­tions, in­clud­ing water tem­per­a­tures up to 36 de­grees Cel­sius and oxy­gen lev­els to 0.2 ppm. They pre­fer habi­tats with veg­e­ta­tion and sub­strate. They sur­vive well in do­mes­ti­cally and in­dus­tri­ally pol­luted wa­ters. They are bot­tom dwelling fish. (Barnes and Hicks, 2003; Becker, 1983; Blazer, et al., 2009a; Blazer, et al., 2009b; Fish­eries and Oceans Canada, 2010; Froese and Pauly, 2010; Page and Burr, 1991)

Phys­i­cal De­scrip­tion

Brown bull­head look very sim­i­lar to black bull­head (Ameiu­rus melas) and yel­low bull­head (Ameiu­rus na­talis). Brown bull­head are dis­tin­guished by 5 to 8 large, ser­rated teeth on their pec­toral spines , mot­tled col­or­ing on their trunk, lack of dark fin rays, and 11 to 15 gill rak­ers on their first gill arch. An oc­ca­sional solid col­ored trunk has been de­scribed. They have 8 dark brown to black bar­bels on their head (two nasal, two max­il­lary, and four on the chin) which are sen­si­tive to touch and chem­i­cal stim­uli. The an­te­rior por­tion of their body is thicker than the pos­te­rior por­tion. The body is scale­less with a brown to black dor­sal side and a lighter ven­tral side. In cap­tiv­ity, this species loses pig­men­ta­tion, be­com­ing whitish. They have ter­mi­nal mouths with a slightly longer upper jaw and a mouth filled with ir­reg­u­lar rows of tiny teeth on both jaws. How­ever, Baily et al. (2004) de­scribed their jaws as being equal. Their head is dorso-ven­trally flat­tened. They have one dor­sal fin, an adi­pose fin, and a cau­dal fin with a slightly in­dented fork. Typ­i­cal adult length is 200 to 300 mm but they may reach up to 500 mm. Adults typ­i­cally weigh 0.5 kg, but have been recorded at 3.6 kg. No sig­nif­i­cant dif­fer­ence has been found be­tween male and fe­male size. (Baily, et al., 2004; Barnes and Hicks, 2003; Becker, 1983; Blumer, 1985; Michi­gan De­part­ment of Nat­ural Re­sources and En­vi­ron­ment, 2010; Nel­son, 1984; Page and Burr, 1991; Rasquin, 1949; Uni­ver­sity of Wis­con­sin Cen­ter for Lim­nol­ogy, et al., 2010)

  • Sexual Dimorphism
  • sexes alike
  • Range mass
    3.6 (high) kg
    7.93 (high) lb
  • Average mass
    0.5 kg
    1.10 lb
  • Range length
    500 (high) mm
    19.69 (high) in
  • Average length
    200-300 mm
    in

De­vel­op­ment

Mean daily water tem­per­a­ture dur­ing re­pro­duc­tion is 14 to 29 de­grees Cel­sius. Once brown bull­head egg clus­ters are re­leased and fer­til­ized, they take up to 13 days to hatch, but did so on av­er­age at day 5.6 dur­ing a study by Blumer (1985). Egg di­am­e­ter is about 2.2 to 2.7 mm. The lar­val stage lasts 4 to 9 days, but on av­er­age lasted 4.4 days in Blumer's study (1985). Hatched lar­vae are 4 to 8 mm long, lay on nests dur­ing early de­vel­op­ment, and sur­vive on their yolk-sacs. Meta­mor­pho­sis oc­curs be­tween the lar­val and ju­ve­nile stage. Ju­ve­niles re­main in schools. The av­er­age length of the ju­ve­nile stage to the end of parental care is 5 days. (Becker, 1983; Blumer, 1985; Ey­cleshymer, 1901)

Re­pro­duc­tion

Brown bull­head are monog­a­mous dur­ing the breed­ing sea­son. Blumer (1985) and Becker (1983) were un­able to de­ter­mine how pair­ing oc­curred. Courtship, oc­cur­ring near nest­ing sites, in­volves hold­ing the part­ners jaw, tail, or head with the mouth, head butting, nib­bling bod­ies, and ca­ress­ing bar­bels. Side-by-side sway­ing has also been ob­served. Pairs set­tle over nests and face away from each other dur­ing ga­mete re­lease. (Becker, 1983; Blumer, 1985; En­cy­clo­pe­dia of Life, 2010)

Brown bull­head spawn once dur­ing the spring and early sum­mer breed­ing sea­son. Dur­ing an ex­ten­sive four year study in Michi­gan by Blumer (1985), this species spawned most fre­quently within the first 16 days of June. He also found that larger males spawned ear­lier in the sea­son. In New Zealand, these fish spawn be­tween Sep­tem­ber and De­cem­ber. They reach sex­ual ma­tu­rity at 3 years of age. Nests, typ­i­cally built by fe­males but some­times by pairs, are ex­ca­va­tions made in the sand, gravel, mud, under roots, and within the shel­ter of logs and veg­e­ta­tion in shal­low water. Sub­strate is sucked into the mouth and re­lo­cated dur­ing nest build­ing. Shel­tered nests are thought to pro­vide pro­tec­tion from preda­tors. Ey­cleshymer (1901) noted nests in pieces of stovepipe and a bucket. Dur­ing nest con­struc­tion males are ter­ri­to­r­ial. Egg clus­ters con­tain 50 to 10,000 eggs. Brown bull­head demon­strate iteropar­ity. Fer­til­iza­tion is ex­ter­nal. (Barnes and Hicks, 2003; Becker, 1983; Blumer, 1985; Ey­cleshymer, 1901; Michi­gan De­part­ment of Nat­ural Re­sources and En­vi­ron­ment, 2010)

  • Breeding interval
    Brown bullhead spawn once during a breeding season.
  • Breeding season
    The breeding season is during the spring and early summer.
  • Range number of offspring
    50 to 10,000
  • Range time to hatching
    13 (high) days
  • Average time to hatching
    5.6 days
  • Average time to independence
    9.4 days
  • Average age at sexual or reproductive maturity (female)
    3 years
  • Average age at sexual or reproductive maturity (male)
    3 years

De­m­er­sal eggs are in­cu­bated and guarded by one or both par­ents who fan the eggs with their fins, which may min­i­mize fun­gal in­fec­tion and help with de­vel­op­ment. After hatch­ing, lar­vae on the nest and school­ing ju­ve­niles are guarded by one or both par­ents who chase away other fish. If ju­ve­niles leave the school, par­ents will cap­ture them and re­turn them with their mouths. Blumer (1985 and 1986a) found males to be pri­mary care­givers: 56.2% of broods were cared for by both sexes, 39.3% by males only, and 4.5% by fe­males only. Max­i­mum length of parental care is 29 days. (Becker, 1983; Blumer, 1985; Blumer, 1986a; Blumer, 1986b)

  • Parental Investment
  • male parental care
  • female parental care
  • pre-fertilization
    • provisioning
    • protecting
      • female
  • pre-hatching/birth
    • provisioning
      • female
    • protecting
      • male
      • female
  • pre-weaning/fledging
    • protecting
      • male
      • female
  • pre-independence
    • protecting
      • male
      • female

Lifes­pan/Longevity

Brown bull­head live 6 to 8 years. Max­i­mum age of brown bull­head is 9 years. Pre­da­tion pres­sure is strongest dur­ing the egg and lar­val stages. (Blumer, 1986b; Froese and Pauly, 2010; Michi­gan De­part­ment of Nat­ural Re­sources and En­vi­ron­ment, 2010)

  • Range lifespan
    Status: wild
    9 (high) years
  • Average lifespan
    Status: wild
    6 to 8 years

Be­hav­ior

Brown bull­head are a non-mi­gra­tory species. They are so­cial fish that spend time in schools. (Blazer, et al., 2009a; Blazer, et al., 2009b)

Home Range

Home range sizes of brown bull­heads are not re­ported.

Com­mu­ni­ca­tion and Per­cep­tion

Brown bull­head are no­table for their sound pro­duc­tion, likely pro­duced by rub­bing body parts to­gether. In the lab, they pro­duce sound dur­ing ag­gres­sive, con­spe­cific en­coun­ters. Sound pro­duc­tion, thought to be a re­sponse to dis­tur­bances, was recorded in the field and iden­ti­fied with cap­tured fish. Grouped in the su­per­order Os­tar­io­physi, they share the de­rived trait of the alarm re­sponse (Shreck­stoff). (An­der­son, et al., 2008; Fine, et al., 1997; Helf­man, et al., 2009)

Food Habits

Brown bull­head are ben­thic, op­por­tunis­tic om­ni­vores. In aquar­ium set­tings they eat most food given to them. Ju­ve­niles eat zoo­plank­ton, in­clud­ing chi­rono­mids, clado­cer­ans, os­tra­cods, and am­phipods, in­sects, in­clud­ing mayfly lar­vae and cad­dis­fly lar­vae, and plants. Adults feed on in­sects, small fish, fish eggs, mol­lusks, plants, leeches, worms, and cray­fish. They typ­i­cally are noc­tur­nal feed­ers, but have been ob­served feed­ing dur­ing the day. They use their bar­bels to lo­cate food. (Barnes and Hicks, 2003; Becker, 1983; Fish­eries and Oceans Canada, 2010; Froese and Pauly, 2010; Kline and Wood, 1996; Raney and Web­ster, 1940)

  • Animal Foods
  • fish
  • eggs
  • insects
  • mollusks
  • terrestrial worms
  • aquatic or marine worms
  • aquatic crustaceans
  • zooplankton

Pre­da­tion

Preda­tors of brown bull­head in­clude north­ern pike (Esox lu­cius), muskel­lunge (Esox masquinongy), wall­eye (Sander vit­reus), snap­ping tur­tles (Chely­dra ser­pentina), water snakes (Nero­dia species), and green herons (Bu­torides virescens). Min­nows (Pimephales and Notro­pis species), yel­low perch (Perca flavescens), and sun­fishes (Lep­omis species) are the most com­mon preda­tors on eggs. (Becker, 1983; Blumer, 1986b; Michi­gan De­part­ment of Nat­ural Re­sources and En­vi­ron­ment, 2010)

  • Anti-predator Adaptations
  • cryptic

Ecosys­tem Roles

Brown bull­head are preda­tory fish and prey on other an­i­mals.

Eco­nomic Im­por­tance for Hu­mans: Pos­i­tive

Brown bull­head are the sub­ject of a small scale recre­ational and com­mer­cial fish­ery in Canada and in the United States. They have been im­por­tant re­search an­i­mals for the study of sen­sory hair cells as well as phys­i­o­log­i­cal changes due to tem­per­a­ture, taste, oxy­gen usage, and os­moreg­u­la­tion. They are also an im­por­tant in­di­ca­tor species in pol­lu­tion stud­ies. (Becker, 1983; Blazer, et al., 2009a; Blazer, et al., 2009b; Bowen, 1931; Chris­tensen, et al., 1972; Fish­eries and Oceans Canada, 2010; Lesko, et al., 1996; Michi­gan De­part­ment of Nat­ural Re­sources and En­vi­ron­ment, 2010; Sakaris and Je­sien, 2005; West, et al., 2006)

  • Positive Impacts
  • food
  • research and education

Eco­nomic Im­por­tance for Hu­mans: Neg­a­tive

There are no known ad­verse ef­fects of brown bull­head on hu­mans.

Con­ser­va­tion Sta­tus

Brown bull­head are not listed for pro­tec­tion under the IUCN Red List, the United States En­dan­gered Species Pro­gram, or under a CITES ap­pen­dix. (In­ter­na­tional Union for Con­ser­va­tion of Na­ture and Nat­ural Re­sources, 2009; U.S. Fish & Wildlife Ser­vice, 2010; United Na­tions En­vi­ron­ment Pro­gramme and World Con­ser­va­tion Mon­i­tor­ing Cen­tre, 2010)

Con­trib­u­tors

Rachael Guth (au­thor), North­ern Michi­gan Uni­ver­sity, Rachelle Ster­ling (ed­i­tor), Spe­cial Pro­jects, Jill Leonard (ed­i­tor), North­ern Michi­gan Uni­ver­sity, Tanya Dewey (ed­i­tor), Uni­ver­sity of Michi­gan-Ann Arbor.

Glossary

Australian

Living in Australia, New Zealand, Tasmania, New Guinea and associated islands.

World Map

Nearctic

living in the Nearctic biogeographic province, the northern part of the New World. This includes Greenland, the Canadian Arctic islands, and all of the North American as far south as the highlands of central Mexico.

World Map

Palearctic

living in the northern part of the Old World. In otherwords, Europe and Asia and northern Africa.

World Map

acoustic

uses sound to communicate

benthic

Referring to an animal that lives on or near the bottom of a body of water. Also an aquatic biome consisting of the ocean bottom below the pelagic and coastal zones. Bottom habitats in the very deepest oceans (below 9000 m) are sometimes referred to as the abyssal zone. see also oceanic vent.

bilateral symmetry

having body symmetry such that the animal can be divided in one plane into two mirror-image halves. Animals with bilateral symmetry have dorsal and ventral sides, as well as anterior and posterior ends. Synapomorphy of the Bilateria.

brackish water

areas with salty water, usually in coastal marshes and estuaries.

carnivore

an animal that mainly eats meat

chemical

uses smells or other chemicals to communicate

cryptic

having markings, coloration, shapes, or other features that cause an animal to be camouflaged in its natural environment; being difficult to see or otherwise detect.

ectothermic

animals which must use heat acquired from the environment and behavioral adaptations to regulate body temperature

external fertilization

fertilization takes place outside the female's body

female parental care

parental care is carried out by females

fertilization

union of egg and spermatozoan

food

A substance that provides both nutrients and energy to a living thing.

freshwater

mainly lives in water that is not salty.

heterothermic

having a body temperature that fluctuates with that of the immediate environment; having no mechanism or a poorly developed mechanism for regulating internal body temperature.

indeterminate growth

Animals with indeterminate growth continue to grow throughout their lives.

introduced

referring to animal species that have been transported to and established populations in regions outside of their natural range, usually through human action.

iteroparous

offspring are produced in more than one group (litters, clutches, etc.) and across multiple seasons (or other periods hospitable to reproduction). Iteroparous animals must, by definition, survive over multiple seasons (or periodic condition changes).

macroalgae

seaweed. Algae that are large and photosynthetic.

male parental care

parental care is carried out by males

metamorphosis

A large change in the shape or structure of an animal that happens as the animal grows. In insects, "incomplete metamorphosis" is when young animals are similar to adults and change gradually into the adult form, and "complete metamorphosis" is when there is a profound change between larval and adult forms. Butterflies have complete metamorphosis, grasshoppers have incomplete metamorphosis.

monogamous

Having one mate at a time.

motile

having the capacity to move from one place to another.

natatorial

specialized for swimming

native range

the area in which the animal is naturally found, the region in which it is endemic.

nocturnal

active during the night

omnivore

an animal that mainly eats all kinds of things, including plants and animals

oviparous

reproduction in which eggs are released by the female; development of offspring occurs outside the mother's body.

piscivore

an animal that mainly eats fish

seasonal breeding

breeding is confined to a particular season

sedentary

remains in the same area

sexual

reproduction that includes combining the genetic contribution of two individuals, a male and a female

social

associates with others of its species; forms social groups.

tactile

uses touch to communicate

temperate

that region of the Earth between 23.5 degrees North and 60 degrees North (between the Tropic of Cancer and the Arctic Circle) and between 23.5 degrees South and 60 degrees South (between the Tropic of Capricorn and the Antarctic Circle).

territorial

defends an area within the home range, occupied by a single animals or group of animals of the same species and held through overt defense, display, or advertisement

tropical

the region of the earth that surrounds the equator, from 23.5 degrees north to 23.5 degrees south.

visual

uses sight to communicate

zooplankton

animal constituent of plankton; mainly small crustaceans and fish larvae. (Compare to phytoplankton.)

Ref­er­ences

Amer­i­can Fish­eries So­ci­ety, 2004. Com­mon and sci­en­tific names of fishes from the United States, Canada, and Mex­ico. Bethesda: Amer­i­can Fish­eries So­ci­ety.

An­der­son, K., R. Roun­tree, F. Juanes. 2008. Sonif­er­ous fishes in the Hud­son River. Trans­ac­tions of the Amer­i­can Fish­eries So­ci­ety, 137: 616-626.

Baily, R., W. Latta, G. Smith. 2004. An atlas of Michi­gan fishes with keys and il­lus­tra­tions for their iden­ti­fi­ca­tion. Ann Arbor: Mu­seum of Zo­ol­ogy, Uni­ver­sity of Michi­gan.

Barnes, G., B. Hicks. 2003. Brown bull­head cat­fish in Lake Taupo. DOC work­shop: 27-35.

Becker, G. 1983. Fishes of Wis­con­sin. Madi­son: Uni­ver­sity of Wis­con­sin Press.

Blazer, V., J. Fournie, J. Wolf, M. Wolfe. 2006. Di­ag­nos­tic cri­te­ria for pro­lif­er­a­tive he­patic le­sions in brown bull­head Ameiu­rus neb­u­lo­sus. Dis­eases of Aquatic Or­gan­isms, 72: 19-30.

Blazer, V., S. Raf­ferty, P. Bau­mann, S. Smith, E. Obert. 2009. As­sess­ment of the "fish tu­mors or other de­for­mi­ties" ben­e­fi­cial use im­pair­ments in brown bull­head (Ameiu­rus neb­u­lo­sus): I. Oro­cu­ta­neous tu­mors. Jour­nal of Great Lakes Re­search, 35: 517-526.

Blazer, V., S. Raf­ferty, P. Bau­mann, S. Smith, E. Obert. 2009. As­sess­ment of the "fish tu­mors or other de­for­mi­ties" ben­e­fi­cial use im­pair­ments in brown bull­head (Ameiu­rus neb­u­lo­sus): II. Liver neo­pla­sia. Jour­nal of Great Lakes Re­search, 35: 527-537.

Blumer, L. 1986. Parental care sex dif­fer­ences in the brown bull­head, Ic­talu­rus neb­u­lo­sus, (Pisces, Ic­taluri­dae). Be­hav­ioral Ecol­ogy and So­cio­bi­ol­ogy, 19: 97-104.

Blumer, L. 1985. Re­pro­duc­tive nat­ural his­tory of the brown bull­head Ic­talu­rus neb­u­lo­sus in Michi­gan. Amer­i­can Mid­land Nat­u­ral­ist, 1985: 318-330.

Blumer, L. 1986. The func­tion of parental care in the brown bull­head Ic­talu­rus neb­u­lo­sus. Amer­i­can Mid­land Nat­u­ral­ist, 115: 234-238.

Bowen, R. 1931. Move­ment of the so-called hairs in the am­pullar or­gans of fish ears. Pro­ceed­ings of the Na­tional Acad­emy of Sci­ence, 17: 192-194.

Chris­tensen, G., J. McKim, E. Hunt. 1972. Changes in the blood of the brown bull­head (Ic­talu­rus neb­u­lo­sus (Lesueur)) fol­low­ing short and long term ex­po­sure to cop­per (II). Tox­i­col­ogy and Ap­plied Phar­ma­col­ogy, 23: 417-427.

En­cy­clo­pe­dia of Life, 2010. "En­cy­clo­pe­dia of Life" (On-line). Ac­cessed Feb­ru­ary 25, 2010 at http.//www.​eol.​org.

Ey­cleshymer, A. 1901. Ob­ser­va­tion on the breed­ing habits of Ameiu­rus neb­u­lo­sus. The Amer­i­can Nat­u­ral­ist, 35: 911-918.

Fine, M., J. Friel, D. McEl­roy, C. King, K. Loesser, S. New­ton. 1997. Pec­toral spine lock­ing and sound pro­duc­tion in the chan­nel cat­fish Ic­talu­rus punc­ta­tus. Copeia, 1997: 777-790.

Fish­eries and Oceans Canada, 2010. "On­tario-Great Lakes area fact sheets" (On-line). Ac­cessed March 09, 2010 at http://​www.​dfo-mpo.​gc.​ca.

Froese, R., D. Pauly. 2010. "Fish­Base" (On-line). Ac­cessed Feb­ru­ary 25, 2010 at http://​www.​fishbase.​org.

Hard­man, M., L. Page. 2003. Phy­lo­ge­netic re­la­tion­ships among bull­head cat­fishes of the Genus Ameiu­rus (Sil­u­ri­formes: Ic­taluri­dae). Copeia, 2003: 20-33.

Helf­man, G., B. Col­lette, D. Facey, B. Bowen. 2009. The di­ver­sity of fishes. United King­dom: Wi­ley-Black­well Pub­li­ca­tion.

In­ter­na­tional Union for Con­ser­va­tion of Na­ture and Nat­ural Re­sources, 2009. "IUCN Red List of Threat­ened Species" (On-line). Ac­cessed March 08, 2010 at http://​www.​iucnredlist.​org.

Kline, J., B. Wood. 1996. Food habits and diet se­lec­tiv­ity of the brown bull­head. Jour­nal of Fresh­wa­ter Ecol­ogy, 11: 145.

Lesko, L., S. Smith, M. Blouin. 1996. The ef­fects of con­t­a­m­i­nated sed­i­ments on fe­cun­dity of the brown bull­head in three Lake Erie trib­u­taries. Jour­nal of Great Lakes Re­search, 22: 830-837.

Michi­gan De­part­ment of Nat­ural Re­sources and En­vi­ron­ment, 2010. "Nat­ural re­sources-fish­ing" (On-line). Ac­cessed March 09, 2010 at http://​michigan.​gov/​dnr.

Nel­son, J. 1984. Fishes of the world. New York: Wi­ley-In­ter­science Pub­li­ca­tion.

Page, L., B. Burr. 1991. Pe­ter­son field guide-fresh­wa­ter fishes. Boston: Houghton Mif­flin Com­pany.

Raney, E., D. Web­ster. 1940. The food and growth of the young of the com­mon bull­head, Ameiu­rus neb­u­lo­sus neb­u­lo­sus (LeSueur). Trans­ac­tions of the Amer­i­can Fish­eries So­ci­ety, 69: 205-209.

Rasquin, P. 1949. Spon­ta­neous de­pig­men­ta­tion in the cat­fish. Copeia, 1949: 246-251.

Sakaris, P., R. Je­sien. 2005. Brown bull­head as an in­di­ca­tor species: sea­sonal move­ment pat­terns and home ranges within the Ana­cos­tia River, Wash­ing­ton, D.C.. Trans­ac­tions of the Amer­i­can Fish­eries So­ci­ety, 134: 1262-1270.

Tomel­leri, J., M. Eberle. 1990. Fishes of the Cen­tral United States. Lawrence: Uni­ver­sity Press of Kansas.

U.S. Fish & Wildlife Ser­vice, 2010. "USFWS En­dan­gered Species Pro­gram" (On-line). Ac­cessed March 08, 2010 at http://​endangered.​fws.​gov/​wildlife.​html.

United Na­tions En­vi­ron­ment Pro­gramme, , World Con­ser­va­tion Mon­i­tor­ing Cen­tre. 2010. "CITES Species Data­base" (On-line). Ac­cessed March 08, 2010 at http://​cites.​org/​eng/​resources/​species.​html.

Uni­ver­sity of Wis­con­sin Cen­ter for Lim­nol­ogy, , Wis­con­sin DNR, Wis­con­sin Sea Grant. 2010. "Wis­con­sin Fish" (On-line). Ac­cessed Feb­ru­ary 25, 2010 at http://​wiscfish.​org.

West, D., N. Ling, B. Hicks, L. Trem­blay, N. Kim, M. Van Den Heuvel. 2006. Cu­mu­la­tive im­pacts as­sess­ment along a large river, using brown bull­head cat­fish (Ameiu­rus neb­u­lo­sus) pop­u­la­tions. En­vi­ron­men­tal Tox­i­col­ogy and Chem­istry, 25: 1868-1880.