Ambloplites rupestrisGoggle eye(Also: Northern rock bass; Redeye; Redeye bass; Rock bass)

Ge­o­graphic Range

Rock bass (Am­blo­plites ru­pestris) are dis­trib­uted through­out North Amer­ica. They are na­tive to the North At­lantic re­gion of the United States and the St. Lawrence, Great Lakes, Hud­son Bay, and Mis­sis­sippi River drainages, as well as north­ern to south­ern Geor­gia and north­ern Al­abama and Mis­souri. Rock bass thrive in areas of the east-cen­tral part of the United States. Al­though they are na­tive to these areas, many in­tro­duc­tions have been made. From 1889 to 1936, the United States Fish Com­mis­sion in­tro­duced rock bass to At­lantic drainages and some west­ern states. Rock bass were in­tro­duced to areas of the At­lantic drainages, from New Hamp­shire, south to the Roanoke River in Vir­ginia and North Car­olina. As for the west­ern states, rock bass have made it to states such as Cal­i­for­nia, Wash­ing­ton, Col­orado, and even Wyoming. Rock bass have also been in­tro­duced in other re­gions. In Eu­rope, rock bass were in­tro­duced in coun­tries such as Eng­land and France in the 1880’s. (Kot­te­lat and Frey­hof, 2007; Page and Burr, 1991)

Habi­tat

Rock bass are found in­hab­it­ing aquatic bio­mes such as rivers, streams, lakes, and ponds. These aquatic bio­mes are fresh­wa­ter, often heav­ily veg­e­tated to pro­vide cover from preda­tors. These fish also thrive in bio­mes with tem­per­a­tures rang­ing from 10 to 29 de­grees Cel­sius. Rock bass are most com­monly dis­trib­uted in re­gions that sup­ply a habi­tat of rocky or sandy char­ac­ter­is­tics in clear water. In re­gions where rock bass are in­tro­duced such as Eu­rope, ecol­o­gists have found their habi­tats to be slightly dif­fer­ent from North Amer­i­can res­i­dents. Rock bass dis­trib­uted in Eu­rope pre­fer sim­i­lar habi­tats, but avoid areas of fast mov­ing water. (Kot­te­lat and Frey­hof, 2007; Page and Burr, 1991)

  • Aquatic Biomes
  • lakes and ponds
  • rivers and streams
  • Range depth
    1.2 (low) m
    3.94 (low) ft

Phys­i­cal De­scrip­tion

Rock bass are part of genus Am­blo­plites, mean­ing “blunt shield,” and the species name ru­pestris refers to their pref­er­ence for being “among the rocks.” Sim­i­lar to other sun­fish, rock bass can be dis­tin­guished by the five to seven spines lo­cated on the anal fin along with nine to eleven soft anal rays. Rock bass also have spines lo­cated on their much larger dor­sal fin, with 10 to 13 spines and 11 to 13 soft dor­sal rays. Rock bass have dis­tin­guish­able dark spots on each scale that are aligned in rows around the lat­eral line, con­tin­u­ing down to­wards the ven­tral side. Start­ing with their back, rock bass are dark green or brown­ish, fad­ing to a lighter green, and slowly fad­ing to whitish green or yel­low to­wards their ven­tral side. Their fins have a yel­low­ish brown tint, with a black spot on the tip of the gill plate. They are rel­a­tively small, av­er­ag­ing about 20 to 25 cm long and very rarely reach one kilo­gram, al­though the largest recorded rock bass was 3 kg. Rock bass have large mouths and bright red eyes, which give them the nick­name “redeyes.” (Kot­te­lat and Frey­hof, 2007; Page and Burr, 1991)

  • Sexual Dimorphism
  • sexes alike
  • Range mass
    3 (high) kg
    6.61 (high) lb
  • Average length
    20 to 25 cm
    in

De­vel­op­ment

Three to four days after spawn­ing, the eggs begin to hatch. At hatch­ing, the mean length of rock bass lar­vae is about 5.5 mm. As the lar­vae grow, melanophores (con­nec­tive-tis­sue cells con­tain­ing melanin, which gives them their color) also begin to de­velop at about 6.8 mm. By about 6.9 mm, the lar­vae begin to de­velop cau­dal fin rays, and dor­sal, anal, and pec­toral fin rays at about 8.6 mm in length. Fi­nally, pelvic fin rays begin to de­velop at about 13.5 mm in length. As the mat­u­ra­tion cycle of the lar­vae con­tin­ues, by the first year, young rock bass grow to about 5 cm in length, reach­ing 10 cm by year two, and up to 18 cm by year three. (Buy­nak and Mohr Jr, 1979)

Re­pro­duc­tion

Rock bass are polyg­y­nan­drous, in which both fe­males and males have mul­ti­ple mates dur­ing the breed­ing sea­son. Rock bass spawn in the spring and, in some cases, spawn again in the early sum­mer with an­other mate. When at­tract­ing a mate, male rock bass find a suit­able area and build a nest. Cir­cling in­side the newly pre­pared nest, the male awaits a mate. With­out courtship dis­plays, the fe­male en­ters the nest and joins the male in his cir­cu­lar be­hav­ior. Both the fe­male and male si­mul­ta­ne­ously re­lease their sperm and eggs into the nest. The fe­male's role in spawn­ing is over after they re­lease eggs and they are able to leave the nest and mate with an­other male, al­though they some­times choose to re­main near the ex­te­rior of the nest. Male rock bass guard and pro­tect the nest using cir­cling be­hav­iors until the fry hatch. (Buy­nak and Mohr Jr, 1979; Gross and Now­ell, 1980)

Sim­i­lar to the spawn­ing cycle of small­mouth bass, rock bass spawn in areas of shal­low water. The spawn­ing cycle of rock bass oc­curs in the spring and into the sum­mer months of June, as the water tem­per­a­ture reaches be­tween 13 to 15 de­grees Cel­sius. Rock bass reach sex­ual ma­tu­rity at about 2 to 3 years of age. Male rock bass pre­pare the nest for spawn­ing. Their nests are cir­cu­lar bowl-shaped de­pres­sions, ap­prox­i­mately 20 to 30 cm in di­am­e­ter. Using their tail, male rock bass are able to clear areas of de­bris to pro­duce their nest. With­out male courtship, fe­males enter the newly-made nest and spawn, re­leas­ing ap­prox­i­mately 500 to 5,000 eggs de­pend­ing on the fe­male's size. After fer­til­iza­tion by the male, the newly spawned eggs are guarded by male rock bass in the in­te­rior of the nest, which con­sists of a 20 to 30 cm area. While guard­ing the eggs, males turn darker in color and con­tinue their cir­cling be­hav­ior, which helps pro­tect the eggs from preda­tors. The eggs begin to hatch 3 to 4 days after spawn­ing and the fry leave the nest ap­prox­i­mately 9 to 10 days after hatch­ing. Ap­prox­i­mately 33% of rock bass nests are un­suc­cess­ful due to pre­da­tion. (Gross and Now­ell, 1980)

  • Breeding interval
    Rock bass reproduce in the spring but it is not uncommon for rock bass to spawn a second time in the early summer.
  • Breeding season
    Rock bass spawn in the spring and summer.
  • Range number of offspring
    500 to 5000
  • Range time to hatching
    3 to 4 days
  • Average time to independence
    9 to 10 days
  • Range age at sexual or reproductive maturity (female)
    2 to 3 years
  • Range age at sexual or reproductive maturity (male)
    2 to 3 years

Male rock bass show parental care by fan­ning the nest with their pec­toral fins and guard­ing and pro­tect­ing the nest by using cir­cling be­hav­iors after spawn­ing with the fe­male. These be­hav­iors con­tinue for sev­eral days, pro­tect­ing the off­spring from preda­tors in hopes of reach­ing a goal of max­i­mum fit­ness. After fe­males lay eggs in the nest, their parental ef­fort is com­plete. (Buy­nak and Mohr Jr, 1979; Gross and Now­ell, 1980)

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

Lifes­pan/Longevity

Rock bass have an av­er­age lifes­pan of about 5 to 8 years in the wild. This av­er­age is ob­vi­ously in­flu­enced by the level of pre­da­tion and food sup­ply in the en­vi­ron­ment. It has been re­ported that the max­i­mum lifes­pan of a rock bass in cap­tiv­ity was 18 years. (Pat­naik et al., 1994)

Be­hav­ior

Dur­ing spawn­ing, male rock bass do not eat. Male rock bass guard the nest of the newly spawned eggs. This nest be­comes their home range, span­ning be­tween 20 and 30 cm in di­am­e­ter. To pro­tect the nest from preda­tors, they per­form cir­cling be­hav­iors. Males are very ag­gres­sive dur­ing spawn­ing sea­son. When faced with a ter­ri­to­r­ial in­truder, they race to­wards it with spread op­er­cles or dis­play an open mouth. In the win­ter months, rock bass can be found in schools and slowly go their sep­a­rate ways as spring ap­proaches for spawn­ing ac­tiv­ity. (Gross and Now­ell, 1980)

  • Range territory size
    20 to 30 cm^2

Home Range

Be­sides the nest ter­ri­tory that males de­fend, no other home ranges have been re­ported. (Gross and Now­ell, 1980)

Com­mu­ni­ca­tion and Per­cep­tion

Fish use chem­i­cal sig­nals to com­mu­ni­cate and per­ceive their en­vi­ron­ment. Rock bass use chemore­cep­tion for a num­ber of com­mu­ni­ca­tion and per­cep­tion tasks. These tasks con­sist of lo­cat­ing prey, iden­ti­fy­ing op­po­site sexes, iden­ti­fy­ing other species, iden­ti­fy­ing pre­da­tion threats and how to avoid these preda­tors, dif­fer­en­ti­at­ing be­tween their young, sig­nal­ing for mi­gra­tion from oth­ers, and even iden­ti­fy­ing where they are in com­par­i­son to their habi­tat. Rock bass use tac­tile char­ac­ter­is­tics or the sense of touch with body parts such as their large, bass-like mouth and even vi­sual char­ac­ter­is­tics such as their big eyes or “gog­gle eyes,” which is an­other com­mon nick­name of rock bass. (Ross, 2013)

Food Habits

Rock bass prey on var­i­ous aquatic species such as plants lo­cated around their highly veg­e­tated habi­tat. Rock bass also prey on small crus­taceans like cray­fish, in­sects such as small lar­vae, and smaller fish, in­clud­ing those of their own species. (Kot­te­lat and Frey­hof, 2007; Page and Burr, 1991)

  • Animal Foods
  • insects
  • aquatic crustaceans

Pre­da­tion

Preda­tors of rock bass in­clude of other, larger adult rock bass, north­ern pike, muskies, walleyes, large­mouth bass, and even hu­mans. These preda­tors prey on adult and young rock bass. To avoid these preda­tors, rock bass de­pend on their cryp­tic col­oration, stay­ing cam­ou­flaged in their en­vi­ron­ment. (Anger­meirer, 1992)

  • Anti-predator Adaptations
  • cryptic

Ecosys­tem Roles

Rock bass feed on in­sects, aquatic crus­taceans, and smaller fish. As a re­sult, the pop­u­la­tions of these or­gan­isms are sup­pressed so that their pop­u­la­tion den­si­ties are at an ac­cept­able level. Rock bass are also hosts in their ecosys­tems. Cope­pods, a small group of crus­taceans that have a par­a­sitic role with rock bass, such as an­chor­worms, de­pend on rock bass. An­chor­worms are ex­ter­nal par­a­sites that embed into the skin of the fish and dam­age and ul­ti­mately de­crease the longevity of rock bass. (Causey, 1957; Kot­te­lat and Frey­hof, 2007; Page and Burr, 1991)

Com­men­sal/Par­a­sitic Species

Eco­nomic Im­por­tance for Hu­mans: Pos­i­tive

Rock bass, along with other bass species, such as small­mouth bass, large­mouth bass, and spot­ted bass, are all sport fish. With com­pet­i­tive tour­na­ment events and even recre­ational events, bass fish­ing has evolved into a multi-bil­lion dol­lar in­dus­try. For ex­am­ple, 33 mil­lion peo­ple of age 16 and older en­gage in the ac­tiv­ity of fish­ing and spend 48 bil­lion dol­lars a year to do so. These sports­men spend this money on fish­ing guides and ser­vices, equip­ment, ap­parel, li­censes, restau­rants, gas, boats, and more. Fish­ing also sup­ports 828,000 jobs in the United States; many of these jobs in­volve fish­ing for species such as rock bass. (Schramm Jr., et al., 1991)

Eco­nomic Im­por­tance for Hu­mans: Neg­a­tive

En­vi­ron­men­tal im­pacts may re­sult from sport fish­ing for rock bass and other species. For ex­am­ple, pol­lu­tion from boats, such as oil and gas leaks, as well as lit­ter­ing by sports­man can take an eco­nomic toll on the ef­forts to main­tain clean and healthy ecosys­tems. (Day­ton, et al., 1995)

Con­ser­va­tion Sta­tus

In­tro­duced into many drainages in the United States, rock bass have flour­ished in their en­vi­ron­ments. As a means of con­ser­va­tion, rock bass are suc­cess­fully sur­viv­ing in their en­vi­ron­ments and are listed as a species of "least con­cern" on the IUCN red list. Rock bass do not re­quire any spe­cial mon­i­tor­ing or con­ser­va­tion man­age­ment plans be­cause of their pop­u­la­tion sta­bil­ity. How­ever, as a sport fish, they are man­aged to some ex­tent. Even though they are not a fish many peo­ple pre­fer to eat, there are slot lim­its (re­quired lengths) on dif­fer­ent bod­ies of water, which reg­u­late whether peo­ple can keep these sport fish. Also, ar­ti­fi­cial nests and nurs­ery/ar­ti­fi­cial ponds are man­age­ment tools de­vel­oped to main­tain pop­u­la­tions of rock bass. (Na­ture­Serve, 2013)

Con­trib­u­tors

Bren­dan Schnell (au­thor), Rad­ford Uni­ver­sity, Karen Pow­ers (ed­i­tor), Rad­ford Uni­ver­sity, Leila Si­cil­iano Mar­tina (ed­i­tor), An­i­mal Di­ver­sity Web Staff.

Glossary

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

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.

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.

ecotourism

humans benefit economically by promoting tourism that focuses on the appreciation of natural areas or animals. Ecotourism implies that there are existing programs that profit from the appreciation of natural areas or animals.

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.

introduced

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

male parental care

parental care is carried out by males

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.

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.

polygynandrous

the kind of polygamy in which a female pairs with several males, each of which also pairs with several different females.

seasonal breeding

breeding is confined to a particular season

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

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

visual

uses sight to communicate

Ref­er­ences

Anger­meirer, P. 1992. Pre­da­tion by rock bass on other stream fishes: ex­per­i­men­tal ef­fects of depth and cover. En­vi­ron­men­tal Bi­ol­ogy of Fishes, 34/2: 171-180.

Beck­man, W. 1943. Fur­ther stud­ies on the in­creased growth rate of the rock bass Am­blo­plites ru­pestris (Rafinesque), fol­low­ing the re­duc­tion in den­sity of the pop­u­la­tion. Trans­ac­tions of the Amer­i­can Fish­eries So­ci­ety, 72/1: 72-78.

Beck­man, W. 1941. In­creased growth rate of rock bass, Am­blo­plites ru­pestris (Rafinesque), fol­low­ing re­duc­tion in the den­sity of the pop­u­la­tion. Trans­ac­tions of the Amer­i­can Fish­eries So­ci­ety, 70/1: 146-148.

Bergman, R. 1942. Fresh Water Bass. New York: Penn Pub­lish­ing Corp.

Bow­ers, G. 1903. U.S. Fish Man­ual. Wash­ing­ton D.C.: Gov­ern­ment Print­ing Of­fice.

Buy­nak, G., H. Mohr Jr. 1979. Lar­val de­vel­op­ment of rock bass from the Susque­hanna River. The Pro­gres­sive Fish Cul­tur­ist, 41/1: 39-42.

Car­lan­der, K., R. Cleary. 1949. The daily ac­tiv­ity pat­terns of some fresh­wa­ter fishes. Amer­i­can Mid­land Nat­u­ral­ist, 41/2: 447-452.

Causey, D. 1957. Par­a­sitic Cope­poda from Louisiana fresh water fish. Amer­i­can Mid­land Nat­u­ral­ist, 58/2: 378-382.

Day­ton, P., S. Thrush, T. Agardy, R. Hof­man. 1995. En­vi­ron­men­tal ef­fects of ma­rine fish­ing. Aquatic Con­ser­va­tion: Ma­rine and Fresh­wa­ter Ecosys­tems, 5/3: 205-232.

George, E., W. Hadley. 1979. Food and habi­tat par­ti­tion­ing be­tween rock bass (Am­blo­plites ru­pestris) and small­mouth bass (Mi­cropterus dolomieu) young of the year. Trans­ac­tions of the Amer­i­can Fish­eries So­ci­ety, 108/3: 253-261.

Ger­ber, G., J. Haynes. 1988. Move­ments and be­hav­ior of small­mouth bass, Mi­cropterus dolomieu, and rock bass, Am­blo­plites ru­pestris, in south­cen­tral Lake On­tario and two trib­u­taries. Jour­nal of Fresh­wa­ter Ecol­ogy, 4/4: 425-440.

Gross, M., W. Now­ell. 1980. The re­pro­duc­tive bi­ol­ogy of rock bass, Am­blo­plites ru­pestris (Cen­trar­chi­dae), in Lake Opini­con, On­tario. Copeia, 1980/3: 482-494.

Kot­te­lat, M., J. Frey­hof. 2007. Hand­book of Eu­ro­pean Fresh­wa­ter Fishes. Switzer­land: Kot­te­lat, Cornol.

Na­ture­Serve, 2013. "Am­blo­plites ru­pestris" (On-line). The IUCN Red List of Threat­ened Species. Ac­cessed April 03, 2014 at www.​iucnredlist.​org.

Near, T., J. Kop­pel­man. 2009. Cen­trar­chid Fishes: Di­ver­sity, Bi­ol­ogy and Con­ser­va­tion. United King­dom: Black­well Pub­lish­ing.

Noltie, D., M. Keen­ley­side. 1986. Cor­re­lates of re­pro­duc­tive suc­cess in stream-dwelling male rock bass, Am­blo­plites ru­pestris (Cen­trar­chi­dae). En­vi­ron­men­tal Bi­ol­ogy of Fishes, 17/1: 61-70.

Page, L., B. Burr. 1991. A Field Guide to Fresh­wa­ter Fishes of North Amer­ica North of Mex­ico. Boston, MA: Houghton Mif­flin Com­pany.

Pat­naik et al., 1994. Age­ing in fishes. Geron­tol­ogy, 40: 113-132.

Pet­ri­moulx, H. 1983. The life his­tory and dis­tri­b­u­tion of the Roanoke bass Am­blo­plites cav­ifrons cope, in Vir­ginia. Amer­i­can Mid­land Nat­u­ral­ist, 110/2: 338-353.

Probst, W., C. Rabeni, W. Cov­ing­ton, R. Marteney. 1984. Re­source use by stream-dwelling rock bass and small­mouth bass. Trans­ac­tions of the Amer­i­can Fish­eries So­ci­ety, 113/3: 283-294.

Roe, K., R. May­den, P. Har­ris. 2008. Sys­tem­at­ics and zoo­geog­ra­phy of the rock basses (Cen­trar­chi­dae: Am­blo­plites). Copeia, 2008/4: 858-867.

Ross, S. 2013. Ecol­ogy of North Amer­i­can Fresh­wa­ter Fishes. Cal­i­for­nia: The Re­gents of the Uni­ver­sity of Cal­i­for­nia.

Sabat, A. 1994. Costs and ben­e­fits of parental ef­fort in a brood-guard­ing fish (Am­blo­plites ru­pestris, Cen­trar­chi­dae). Be­hav­ioral Ecol­ogy, 5/2: 195-201.

Schramm Jr., H., M. Arm­strong, N. Fu­ni­celli, D. Green, D. Lee, R. Manns Jr., B. Taubert, S. Wa­ters. 1991. The sta­tus of com­pet­i­tive sport fish­ing in North Amer­ica. Fish­eries, 16/3: 4-12.