Myoxocephalus thompsoniiDeepwater sculpin

Ge­o­graphic Range

Al­though there are sim­i­lar Nearc­tic and Palearc­tic species, as well as sim­i­lar Eu­ro­pean fresh­wa­ter species, deep­wa­ter sculpin, My­ox­o­cephalus thomp­sonii are lim­ited to North Amer­ica. Once abun­dant in the Great Lakes and most deep lakes of Canada (es­pe­cially Nip­igon in On­tario, Great Slave in Man­i­toba, Wa­ter­ton in Al­berta, and Great Bear in the North­west Ter­ri­to­ries), the ge­o­graphic range of deep­wa­ter sculpin is rapidly shrink­ing.

At pre­sent, deep­wa­ter sculpin are plen­ti­ful in lakes Huron, Michi­gan and Su­pe­rior, and rare in On­tario and Erie. De­spite their deep­wa­ter habi­tat re­quire­ments, they are also found oc­ca­sion­ally in the in­land wa­ter­ways that con­nect the Great Lakes, such as the St. Claire River.

Habi­tat

Dur­ing their first year, deep­wa­ter sculpin are pelagic, rather than ben­thic or­gan­isms. They live in the water col­umn feed­ing on pelagic phy­to­plank­ton and small in­ver­te­brates. As they age they un­dergo phys­i­o­log­i­cal changes and be­come ben­thic or­gan­isms.

Adult deep­wa­ter sculpin are gen­er­ally found in wa­ters deeper than 20 me­ters and are par­tic­u­larly abun­dant be­tween 70 and 90 me­ters. In Lake Su­pe­rior they have been found at depths of 407 me­ters. Al­though all adults are ben­thic, the largest fish of a pop­u­la­tion are found in the deep­est wa­ters. Deep­wa­ter sculpin live only in cold water, 40 de­grees Cel­sius or less.

Due to their ben­thic habi­tat, deep­wa­ter sculpin spend their adult lives in com­plete dark­ness where the tem­per­a­ture ranges be­tween 3 and 6 de­grees Cel­sius. At this depth, the bot­tom sub­strate is fine par­tic­u­late mat­ter, mud and clays of a uni­form size. When they were much more plen­ti­ful, they could also be found on sub­strates con­sist­ing of com­bi­na­tions of sand, silt, clay and mud in­ter­mixed with rocks, coal and cin­ders. Dur­ing one study in 1952, they were found in the wa­ters off Mu­nis­ing, Michi­gan, on thick beds of aquatic veg­e­ta­tion (Ja­coby 1953).

  • Range depth
    20 to 407 m
    65.62 to 1335.30 ft
  • Average depth
    70-90 m
    ft

Phys­i­cal De­scrip­tion

Deep­wa­ter sculpin have been known to reach 9 inches (23 cm) in length, al­though the av­er­age is be­tween 2 and 5 inches (5 to 10 cm). The body is slen­der with a large flat­tened head and blunt snout with a large mouth. Eyes are set close to­gether on top of the flat­tened head. There are four pre­op­er­cu­lar spines, the two upper ones so close to­gether as to be mis­taken as one (Brandt, 1986). There are two dor­sal fins, the sec­ond sig­nif­i­cantly larger than the first. In ma­ture males, this sec­ond dor­sal fin often over­laps the base of the cau­dal fin, and is one of the dis­tin­guish­ing char­ac­ter­is­tics of deep­wa­ter sculpin (Page et al., 1991). Al­though deep­wa­ter sculpin have no scales, they do have prick­les on top of the body.

Col­oration is largely char­ac­ter­is­tic of what one would ex­pect in a habi­tat with very lit­tle if any light. The dor­sal re­gion is gray-brown, while the ven­tral is sev­eral shades lighter. The top and sides are speck­led and there are thin oval shaped-marks dot­ting the back (Page et al., 1991).

Sex­ual di­mor­phism is ap­par­ent only in sex­u­ally ma­ture in­di­vid­u­als. The largest fish tend to be the most sex­u­ally di­mor­phic in the de­vel­op­ment of the fins. “In order of de­creas­ing mag­ni­tude, it is most pro­nounced in the sec­ond dor­sal, pelvic, anal, first dor­sal, pec­toral, and cau­dal fins” (Ja­coby, 1953). (Ja­coby, 1953; Page and Burr, 1991)

  • Sexual Dimorphism
  • sexes alike
  • Range length
    23 (high) cm
    9.06 (high) in

De­vel­op­ment

Al­though re­search is on­go­ing, due to the deep­wa­ter sculpin’s in­ac­ces­si­ble habi­tat, there is lit­tle con­crete doc­u­men­ta­tion of their de­vel­op­men­tal stages.

On­to­ge­netic changes occur dur­ing the deep­wa­ter sculpin’s first year of life, trans­form­ing them from pelagic larva to ben­thic or­gan­isms as ju­ve­niles, and even­tu­ally as adults (Bruch, 1986).

Size in­crease is great­est in the first year. Dur­ing the sec­ond and third years of life, size in­crease is typ­i­cally three-fifths that of the first year. In suc­ces­sive years, the length in­crease was less than two-fifths that of the first year. On the other hand, weight gain is in­versely re­lated to length in­crease. Deep­wa­ter sculpin put on the least weight in the first year, de­spite the great­est gain in length. In suc­ces­sive years, as elon­ga­tion slows, weight gain in­creases (Sel­geby, 1988). The largest fish tend to be the old­est.

Re­pro­duc­tion

Be­cause it is so dif­fi­cult to study deep­wa­ter sculpin, lit­tle is known about their mat­ing sys­tems.

Sex­ual ma­tu­rity does not occur dur­ing the first grow­ing sea­son. In­stead, after be­com­ing ben­thic or­gan­isms, go­nads begin to de­velop dur­ing the sec­ond half of the sec­ond grow­ing sea­son. Even at this rate, less than half of this age group is fully ma­ture by fall of their sec­ond year. The re­main­der of the fish be­come fully sex­u­ally ma­ture by the fall of their third year (Sel­geby, 1988).

Deep­wa­ter sculpin spawn dur­ing late fall and win­ter in the Great Lakes and dur­ing sum­mer and early fall in Canada (Black et al., 1981). The av­er­age num­ber of eggs found in the ovaries of ripe fe­males (fe­males who are just about to lay eggs) is 481. As in other as­pects of sculpin life, size does mat­ter and the largest fe­males have the great­est num­bers of eggs. Eggs range in size from 1.5 to 2.2 mm (Ja­coby, 1953). In the Great Lakes the eggs hatch at the same time that the ice on the lakes be­gins to break up. (Black and Lankester, 1981; Sel­geby, 1988)

  • Breeding interval
    Breeding is likely to occur each year.
  • Breeding season
    Breeding occurs in late fall and winter.
  • Average number of offspring
    481
  • Range age at sexual or reproductive maturity (female)
    2 (low) years
  • Average age at sexual or reproductive maturity (female)
    3 years
  • Range age at sexual or reproductive maturity (male)
    2 (low) years
  • Average age at sexual or reproductive maturity (male)
    3 years

Like other sculpin species, male deep­wa­ter sculpin build nests and guard the eggs.

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

Lifes­pan/Longevity

The gen­eral method for de­ter­min­ing age has been to count the an­nual ‘rings’ on the otolith. Ac­cord­ing to data col­lected in the sum­mer of 1973, the max­i­mum age for deep­wa­ter sculpin in the Great Lakes was seven years. More re­cent re­search sug­gests that al­ter­nat­ing clear and dark bands on the otolith re­flect rapid growth dur­ing the sum­mer and much slower growth dur­ing the win­ter. (Sel­geby, 1988)

  • Typical lifespan
    Status: wild
    7 (high) years

Be­hav­ior

These fish live in cold, deep wa­ters and very lit­tle is known about their be­hav­ior.

Com­mu­ni­ca­tion and Per­cep­tion

Deep­wa­ter sculpin live in very dark en­vi­ron­ments. Lit­tle is known about their modes of per­cep­tion and how they might com­mu­ni­cate, but it is likely that they use tac­tile and chem­i­cal per­cep­tion in their dark habi­tat.

Food Habits

Data on food pref­er­ence is based on stom­ach con­tents of cap­tured fish. The most promi­nent food item in all spec­i­mens ex­am­ined was the am­phi­pod Pon­to­por­eia hoyi. Also often con­sumed were opos­sum shrimp, Mysis re­licta (Black et al., 1981). An over­whelm­ing pro­por­tion of the diet of large deep­wa­ter sculpins is made up of P. hoyi com­pared to the diet of smaller sculpins which feed fairly equally on P. hoyi and M. re­licta (Brandt, 1986 and Wo­j­cik et al., 1986). (Brandt, 1986)

  • Primary Diet
  • carnivore
    • eats non-insect arthropods
  • Animal Foods
  • aquatic crustaceans

Pre­da­tion

Preda­tors of deep­wa­ter sculpin in­clude lake trout (Salveli­nus na­may­cush) and bur­bot (Lota lota) (McAl­lis­ter et al., 1979). By the early 1950s, lake trout and bur­bot were nearly ex­tir­pated from Lake On­tario after falling vic­tim to over-fish­ing and sea-lam­prey par­a­sitism. Shortly after the pop­u­la­tion de­clines of these two key­stone preda­tors, deep­wa­ter sculpin dis­ap­peared from Lake On­tario for al­most the next 50 years. It is be­lieved that the loss of these key­stone preda­tors re­sulted in huge dis­rup­tions to this fresh­wa­ter fish com­mu­nity and deep pop­u­la­tion de­clines of sculpin.

Anti-pre­da­tion mech­a­nisms have barely been stud­ied in deep­wa­ter sculpin. The prick­les on the top of the body and the four spines on top of the head may serve as de­ter­rents to preda­tors. In ad­di­tion, the fact that deep­wa­ter sculpin spend most of their time under con­di­tions few other species can with­stand, lim­its their in­ter­ac­tion with po­ten­tial preda­tors.

Ecosys­tem Roles

Deep­wa­ter sculpin are the num­ber one prey item for lake trout (Salveli­nus na­may­cush), a once widely avail­able, com­mer­cially har­vested fish found in all the Great Lakes. Al­though a con­certed ef­fort has been made since 1950 to re­store lake trout pop­u­la­tions to the Great Lakes, suc­cess has been spotty and lim­ited. Nat­ural re­pro­duc­tion of lake trout is cur­rently oc­cur­ring on a wide­spread basis only in Lake Su­pe­rior. In Lakes Huron, Michi­gan and On­tario, only lim­ited nat­ural re­pro­duc­tion has oc­curred. Of these three, only in Lake Huron do the lar­val fish sur­vive into adult­hood (USGS, 2001).

Due to their role as key for­age items for lake trout and bur­bot and be­cause M. re­licta and P. hoyi are their main food sources, deep­wa­ter sculpin are thought to be re­spon­si­ble for fa­cil­i­tat­ing the ma­jor­ity of the en­ergy move­ment from ben­thic or­gan­isms to higher trophic lev­els. This ob­scure but crit­i­cal role is likely to have far rang­ing in­flu­ences on the over­all pro­duc­tiv­ity of the en­tire Great Lakes ecosys­tem.

It may be that com­pe­ti­tion be­tween sculpin species con­tributed to a de­cline in deep­wa­ter sculpin. Data on com­pet­i­tive feed­ing habits of var­i­ous sculpin species are lim­ited, how­ever, ju­ve­nile deep­wa­ter sculpin and slimy sculpin (Cot­tus cog­na­tus) have over-lap­ping food pref­er­ences and habi­tat use, cre­at­ing the po­ten­tial for com­pe­ti­tion. There is also ev­i­dence that slimy sculpin prey on the eggs and lar­vae of deep­wa­ter sculpin. (Brandt, 1986)

Eco­nomic Im­por­tance for Hu­mans: Pos­i­tive

Deep­wa­ter sculpin cur­rently are not seen as hav­ing any com­mer­cial value or eco­nomic im­por­tance on a local, na­tional or in­ter­na­tional scale. They are im­por­tant mem­bers of the na­tive Great Lakes and north­ern lakes ecosys­tem.

Eco­nomic Im­por­tance for Hu­mans: Neg­a­tive

There are no known neg­a­tive af­fects of deep­wa­ter sculpin on hu­mans.

Con­ser­va­tion Sta­tus

From 1942 to 1972, no deep­wa­ter sculpin were cap­tured in Lake On­tario so far as is known. Be­tween 1972 and 2002, only six have been caught there, de­spite con­tin­ued gov­ern­ment man­dated trawls aimed at de­ter­min­ing the ex­tent of their ex­tir­pa­tion from the Great Lakes. All six were caught in Cana­dian wa­ters, three in 1972 and three in 1996 (Black et al. 1981).

De­spite their dis­ap­pear­ance from Lake On­tario and steady de­cline in the other Great Lakes, the United States Fish and Wildlife Ser­vice (USFWS) does not list deep­wa­ter sculpin as even being a species of con­cern for the Great Lakes re­gion (NYS­DEC, 2002). They are how­ever, listed by the New York State De­part­ment of En­vi­ron­men­tal Con­ser­va­tion and the Cana­dian gov­ern­ment as being threat­ened and mon­i­tored (NYS­DEC, 2002, COSEWIC, 2001). Re­search ef­forts are un­der­way to de­ter­mine how many deep­wa­ter sculpin are left in the Great Lakes and the other deep water lakes of Canada. The de­cline of deep­wa­ter sculpin may have been linked to the in­tro­duc­tion of two non-na­tive species in the Great Lakes: alewives and rain­bow smelt. Both of those fish species eat deep­wa­ter sculpin eggs and com­pete with them for food.

There are cur­rently two known threats to the con­tin­ued sur­vival of deep­wa­ter sculpin. The first is the loss of the am­phi­pod Pon­to­por­eia from the ma­jor­ity of the bot­tom of Lake Michi­gan. As one of their main food sources, the loss of this im­por­tant food source will sub­stan­tially im­pact the re­cruit­ment of deep­wa­ter sculpin. The sec­ond threat is the pres­ence of in­va­sive round go­b­ies in off-shore wa­ters that over­lap the dis­tri­b­u­tion of spawn­ing sites for deep­wa­ter sculpin. Round go­b­ies are fierce fight­ers, and often out-com­pete sculpin species in the same area (Jude et al., 2002).

Con­trib­u­tors

William Fink (ed­i­tor), Uni­ver­sity of Michi­gan-Ann Arbor, Tanya Dewey (ed­i­tor), An­i­mal Di­ver­sity Web.

Alexan­dra Be­linky (au­thor), Uni­ver­sity of Michi­gan-Ann Arbor.

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

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.

carnivore

an animal that mainly eats meat

chemical

uses smells or other chemicals to communicate

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

fertilization

union of egg and spermatozoan

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.

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).

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.

oviparous

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

pelagic

An aquatic biome consisting of the open ocean, far from land, does not include sea bottom (benthic zone).

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

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).

Ref­er­ences

"New York State De­part­ment of En­vi­ron­men­tal Con­ser­va­tion" (On-line). Ac­cessed No­vem­ber 19, 2002 at http://​www.​dec.​state.​ny.​us/​website/​dfwmr/​fish/​fishspecs/​endgtext.​html#​deepwatersculpin.

"Sci­en­tific Com­mit­tee on the Sta­tus of En­dan­gered Wildlife in Canada (COSEWIC)" (On-line). Ac­cessed No­vem­ber 19, 2002 at http://​www.​speciesatrisk.​gc.​ca/​media/​back3_​e.​cfm.

Black, G., M. Lankester. 1981. The bi­ol­ogy and par­a­sites of deep­wa­ter sculpin, *My­ox­o­cephalus quadri­cor­nis thomp­sonii* (Gi­rard), in Burchell Lake, On­tario. Cana­dian Jour­nal of Zo­ol­ogy,, vol. 59 (7): 1454-1456.

Brandt, S. 1986. Dis­ap­pear­ance of the deep­wa­ter sculpin (*My­ox­o­cephalus thomp­sonii*) from Lake On­tario: the key­stone preda­tor hy­poth­e­sis. Jour­nal of Great Lakes Re­search,, vol. 12 (11): 18-24.

Bruch, R. 1986. Age and Growth, Mor­tal­ity, Re­pro­duc­tive Cycle and Fe­cun­dity of the Deep­wa­ter Sculpin, My­ox­o­cephalus thomp­sonii (Gi­rard), in Lake Michi­gan. Mil­wau­kee, Wis­con­sin: Uni­ver­sity of Wis­con­sin - Mil­wau­kee.

Cross­man, E., H. Van Meter. 1979. An­no­tated List of the Fishes of the Lake Onatario Wa­ter­shed. Ann Arbor, MI: Great Lakes Fish­eries Com­mi­sion.

Ja­coby, C. 1953. Notes on the Life His­tory of the Deep­wa­ter Sculpin, My­ox­o­cephalus quadri­cor­nis L., in Lake Su­pe­rior. Ann Arbor, Michi­gan: De­part­ment of Fish­eries, School of Nat­ural Re­sources, Uni­ver­sity of Michi­gan.

Momot, W., S. Stephen­son. 1996. Atlas of the Dis­tri­b­u­tion of the Fish within th Cana­dian Trib­u­taries of West­ern Lake Su­pe­rior. Toronto, On­tario, Canada: Uni­ver­sity of Toronto.

Page, L., B. Burr. 1991. A field guide to fresh­wa­ter fishes of North Amer­ica. Boston, Mass­a­chu­setts: Houghton Mif­flin Com­pany.

Sel­geby, J. 1988. Com­par­a­tive bi­ol­ogy of the sculpins of Lake Su­pe­rior. Jour­nal of Great Lakes Re­search,, vol. 14 (1): 45-51.

Wo­j­cik, J., M. Evans, D. Jude. 1986. Food of deep­wa­ter sculpin, *My­ox­o­cephalus thomp­sonii*, from South­east­ern Lake Michi­gan. Jour­nal of Great Lakes Re­search, vol. 12 (3): 225-231.