Gasterosteus aculeatus

Ge­o­graphic Range

The three­spine stick­le­back fish (Gas­teros­teus ac­ulea­tus) are in ma­rine, brack­ish and coastal fresh­wa­ter habi­tats of the north­ern hemi­sphere. They are found in bo­real and tem­per­ate re­gions of the north­ern hemi­sphere and in ma­rine wa­ters and low­land fresh­wa­ter habi­tats in the At­lantic and Pa­cific basins.

In the At­lantic Ocean, three­spine stick­le­backs are dis­trib­uted from the Iber­ian Penin­sula through the British Isles to Ice­land and south­ern Green­land, and south along the east coast of North Amer­ica to Chesa­peake Bay. Fresh­wa­ter pop­u­la­tions are found through­out most of this range, but do not go far­ther south than Maine, USA. Fresh­wa­ter pop­u­la­tions are also dis­trib­uted along the coast of the Mediter­ranean and in in­land wa­ters across East­ern Eu­rope to the Baltic Sea.

In the Pa­cific Ocean, three­spine stick­le­backs are found from Baja Cal­i­for­nia, Mex­ico north­ward along the coast of North Amer­ica, across the Bering Strait, and then along the coast of main­land Asia and Japan to the south­west coast of Korea. Ma­rine and fresh­wa­ter pop­u­la­tions are found in Japan, but the limit of ma­rine pop­u­la­tions in Asia is un­clear. Fresh­wa­ter pop­u­la­tions are re­stricted to coastal areas in both Asia and North Amer­ica. (Baker, et al., 1995; Bell, et al., 1994; Cresko, et al., 2007; Walker, 1997)

Habi­tat

Gas­teros­teus ac­ulea­tus oc­cupy a wide range of habi­tats. They have been found in small, ephemeral streams in south­ern Cal­i­for­nia and in more per­ma­nent flow­ing wa­ters of vari­able sizes. These fish do not tol­er­ate high-gra­di­ent streams, and they are rarely found in habi­tats more than a few hun­dred me­ters above sea level. In fresh­wa­ter lakes, they are di­vided into ben­thic and lim­netic eco­types. Ben­thic en­vi­ron­ments in­clude shal­low, rel­a­tively eu­trophic lakes or the lit­toral zone of deeper lakes. Lim­netic eco­types are typ­i­cally found in the water col­umn of deep olig­otrophic lakes. Ma­rine fish in­habit the open ocean. (Bell, et al., 1994; Mat­tern, et al., 2007; Shaw, et al., 2007)

Phys­i­cal De­scrip­tion

Phys­i­cal de­scrip­tion varies widely with age and habi­tat. In gen­eral, three­spine stick­le­backs tend to be stream­lined and less than 10 cm long (usu­ally from 3 to 8 cm). Fresh­wa­ter pop­u­la­tions vary in body shape, de­pend­ing on the habi­tat they oc­cupy. Lim­netic eco­types tend to have slen­der bod­ies with nar­row mouths, long snouts, and large eyes. Ben­thic eco­types tend to be deep-bod­ied, with a wide, ter­mi­nal gape.

The fish can have a ro­bust set of spines, a pelvic gir­dle, and nu­mer­ous lat­eral bony plates (up to thirty or more on each side), but the ex­tent of these fea­tures varies by pop­u­la­tion. Dor­sal and pelvic spines vary in num­ber, place­ment, and length, and the spines tend to be longer in pop­u­la­tions that co-oc­cur with preda­tory fishes. The pelvic gir­dle con­sists of a bi­lat­eral struc­ture with an an­te­rior process that has an as­cend­ing branch on each side, a pos­te­rior process and a spine and fin ray. The ab­domen is ringed in bony armor. Ma­rine fish al­most al­ways pos­sess a fully de­vel­oped pelvic gir­dle and a full com­ple­ment of bony lat­eral plates. How­ever, many fresh­wa­ter pop­u­la­tions have re­duced armor plates and pelvic gir­dles, and some pop­u­la­tions have lost these fea­tures en­tirely.

Al­though body color also varies among pop­u­la­tions, three­spine stick­le­backs are gen­er­ally cryp­tic, with brown-to-green bar­ring above and paler col­or­ing below. As males ap­proach re­pro­duc­tive con­di­tion, they be­come less cryp­tic, and their eyes be­come an iri­des­cent blue. In some pop­u­la­tions, red col­oration may ex­pand onto the flanks be­hind the pec­toral fin. (Baker, et al., 1995; Bell, et al., 1994; Cresko, et al., 2007; Day, et al., 1994)

  • Sexual Dimorphism
  • sexes alike
  • sexes colored or patterned differently
  • male more colorful
  • Range length
    3 to 8 cm
    1.18 to 3.15 in
  • Average length
    5 cm
    1.97 in

De­vel­op­ment

Once eggs are fer­til­ized, they take be­tween 5 and 10 days to hatch, de­pend­ing on the tem­per­a­ture of the water. Upon hatch­ing, three­spine stick­le­back lar­vae are about 4 mm in length. The lar­vae will con­tinue to grow by ab­sorp­tion of the yolk, which they will com­pletely con­sume about four days after hatch­ing. Ap­prox­i­mately nine days after hatch­ing, the lar­vae reach a length of about 8 mm and as­sume the shape of the adult fish. This is the ju­ve­nile stage, in which the im­ma­ture young be­come in­de­pen­dent of their fa­ther. Ju­ve­niles be­come adults when they reach sex­ual ma­tu­rity, which is usu­ally within 1 to 2 years of hatch­ing. (Bell, et al., 1994; Swarup, 1958)

Re­pro­duc­tion

Prior to the onset of breed­ing, males will de­velop a re­pro­duc­tive phe­no­type, in­clud­ing blue eyes, red throats, and red fore-bel­lies. Dur­ing the breed­ing sea­son, a male will leave the shoal and set­tle on the bot­tom in shal­low water, where he will con­struct a nest and es­tab­lish a ter­ri­tory. The males are are gen­er­ally not monog­a­mous, and a male often tries to lead nu­mer­ous fe­males into his nest to lay eggs. Af­ter­ward, he will fer­til­ize all the eggs at once.

Males at­tract fe­males with zig-zag-like courtship dances, and fe­males re­spond with a form of danc­ing, as well as a "head-up" pos­ture. The male will then lead the fe­male to his nest, lying on the sub­strate next to the en­trance to sig­nify that she may enter and lay her eggs. Fe­males lay their eggs in the male’s nest and then leave the male alone to at­tend to the eggs until they hatch. Once eggs are fer­til­ized, they may take five to ten days to hatch, de­pend­ing on the tem­per­a­ture of the water. The male nest­ing cycle con­sists of a sex­ual phase for 1 to 4 days, and then a parental phase after the eggs are fer­til­ized. (Bell, et al., 1994; Mat­tern, et al., 2007)

Three­spine stick­le­backs breed in sloughs, ponds, rivers, lakes, drainage canals, marshes, tidal creeks and sub­lit­toral zones of the sea. In­di­vid­u­als reach sex­ual ma­tu­rity at be­tween 1 and 2 years of age, and breed­ing oc­curs an­nu­ally from late April to July. (Bell, et al., 1994; Mat­tern, et al., 2007)

  • Breeding interval
    Threespine stickleback generally breed once yearly
  • Breeding season
    late April to July
  • Range time to hatching
    5 to 10 days
  • Average time to independence
    2 weeks
  • Range age at sexual or reproductive maturity (female)
    1 to 2 years
  • Range age at sexual or reproductive maturity (male)
    1 to 2 years

Once males shift to their parental phase, they pro­vide all the care for their young. This in­cludes fan­ning eggs with their pec­toral fins to pro­vide oxy­gen for the de­vel­op­ing em­bryos and pro­tect­ing them from preda­tors. They also con­vert the nest into a nest pit, which con­sists of tan­gled veg­e­ta­tion where newly hatched fry can hide and rest. The males typ­i­cally de­fend the fry up to two weeks after hatch­ing. Pa­ter­nal care has been iden­ti­fied as an im­por­tant so­cial fac­tor in three­spine stick­le­back de­vel­op­ment and learn­ing. Stick­le­backs with no pa­ter­nal con­tact tend to fail avoid­ing preda­tors later in life. These anti-preda­tor be­hav­iors may be stim­u­lated at an early age as stick­le­back fa­thers chase and catch their fry when they first emerge from the nest. (Bell, et al., 1994; Hunt­ing­ford and Wright, 1993)

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

Lifes­pan/Longevity

Lifes­pans of three­spine stick­le­backs have been recorded in a large num­ber of stud­ies, but the re­sults vary. A de­fin­i­tive pat­tern for the lifes­pan has not been de­ter­mined. Three­spine stick­le­backs can live to ap­prox­i­mately five years in the lab­o­ra­tory. One in­di­vid­ual reached eight years of age in cap­tiv­ity. (Bell, et al., 1994)

  • Range lifespan
    Status: captivity
    8 (high) years
  • Average lifespan
    Status: captivity
    5 years
  • Average lifespan
    Status: captivity
    5 years

Be­hav­ior

Three­spine stick­le­backs tend to ex­hibit shoal­ing so­cial be­hav­iors in the lab and in the field. Stick­le­back fry usu­ally join groups con­tain­ing fa­mil­iar, or ge­net­i­cally sim­i­lar in­di­vid­u­als and show a pref­er­ence for sib­lings as op­posed to non-sib­lings. Three­spine stick­le­backs use the shoals as pro­tec­tion when they for­age and in their vig­i­lance for preda­tors.

Three­spine stick­le­backs ex­hibit vari­able be­hav­ior de­pend­ing on their habi­tat and mor­phol­ogy. Much re­search has been con­ducted on the amount of armor in stick­le­backs and its cor­re­la­tion with their re­sponses to preda­tors. (Mat­tern, et al., 2007; Peuhkuri, 1998)

Home Range

Many ma­rine three­spine stick­le­backs are anadro­mous and mi­grate from off­shore habi­tats to breed in tidal pools, low­land lakes, and fresh­wa­ter wet­lands. Cur­rent fresh­wa­ter pop­u­la­tions were likely founded when some fish re­mained in fresh­wa­ter lakes dur­ing the last glacial melt. (Bell, et al., 1994)

Com­mu­ni­ca­tion and Per­cep­tion

Three­spine stick­le­backs rely on vi­sual cues for mat­ing be­hav­ior. Fe­males tend to be at­tracted to more red­dish col­or­ing of males dur­ing mat­ing sea­sons. They also use ol­fac­tory sig­nals to de­tect the pres­ence of con­specifics, prey, and preda­tors. Like many other fish, three­spine stick­le­backs use alarm cues to avoid pre­da­tion and sex pheromones dur­ing breed­ing. Lab-raised stick­le­backs have been found to rely heav­ily on ol­fac­tory cues of kin­ship, habi­tat and diet, and shoal size. How­ever, the sen­sory or­gans and path­ways uti­lized in this com­mu­ni­ca­tion are not well un­der­stood. (Mat­tern, et al., 2007)

Food Habits

Three­spine stick­le­backs are gen­er­al­ist car­ni­vores and prey on lim­netic and lit­toral in­ver­te­brates. Lim­netic eco­types in lentic en­vi­ron­ments feed on zoo­plank­ton, while ben­thic eco­types feed on bot­tom-dwelling in­ver­te­brates in the lit­toral zone. Com­mon ben­thic prey items in­clude crus­taceans (Am­phipoda) and lar­val in­sects (Chi­rono­mi­dae). Three­spine stick­le­back ex­hibit a pre­da­tion cycle that con­sists of search, pur­suit, at­tack, and cap­ture com­po­nents. (Cresko, et al., 2007; Walker, 1997)

  • Animal Foods
  • eggs
  • insects
  • aquatic or marine worms
  • aquatic crustaceans
  • zooplankton

Pre­da­tion

Three­spine stick­le­backs are small, abun­dant, and slow swim­mers, all of which com­bine to make them suit­able prey for many dif­fer­ent preda­tors. How­ever, they have evolved sev­eral preda­tor de­fenses in their mor­phol­ogy and be­hav­ior. Anti-preda­tor mor­phol­ogy in­cludes dor­sal spines, bony lat­eral plates, and a pelvic gir­dle that con­sists of a pair of an­te­rior processes with as­cend­ing branches, pos­te­rior processes and pelvic spines. Be­hav­ioral re­sponses to pre­da­tion risk in­clude school­ing, re­main­ing close to pro­tec­tive cover, and preda­tor in­spec­tion. Anti-preda­tor mor­phol­ogy and be­hav­iors tend to be more well-de­vel­oped in fish from en­vi­ron­ments that con­tain preda­tors. (Grand, 2000; Marchinko, 2008; Reim­chen, 2000)

Known preda­tors of three­spine stick­le­backs in­clude fish in the fam­i­lies Per­ci­dae, Es­o­ci­dae, and Salmonidae. Some lakes in Alaska and British Co­lum­bia have been stocked with rain­bow trout (On­corhynchus mykiss) and sil­ver salmon (On­corhynchus kisutch) for game, and these fish prey on stick­le­backs in those lakes. Avian pis­ci­vores that prey on stick­le­back fish in­clude loons (Gavi­iformes), grebes (Pod­ici­ped­i­formes), the com­mon mer­ganser (Mer­gus mer­ganser), herons (Ardei­dae), and king­fish­ers (Al­ce­dinidae). Pis­civ­o­rous macroin­ver­te­brates, such as drag­on­fly na­iads (Odonata) and bee­tles (Coleoptera) feed on eggs, fry and ju­ve­nile stick­le­backs. Leeches (Hirudinea) prey on stick­le­back eggs and have also been found to con­sume adult stick­le­backs stuck in traps. (Bell, et al., 1994; Messler, et al., 2007)

  • Anti-predator Adaptations
  • cryptic

Ecosys­tem Roles

Three­spine stick­le­backs have many preda­tors and are thus an im­por­tant source of food for many dif­fer­ent an­i­mals. They also act as preda­tors for ben­thic in­ver­te­brates, such as am­phipods and in­sect lar­vae. (Cresko, et al., 2007; Messler, et al., 2007; Walker, 1997; Ward, et al., 2005)

Com­men­sal/Par­a­sitic Species
  • tape­worm (Schis­to­cephalus solidus)

Eco­nomic Im­por­tance for Hu­mans: Pos­i­tive

Three­spine stick­le­backs have been widely stud­ied in terms of spe­ci­a­tion and evo­lu­tion­ary his­tory be­cause of their phy­logeny and adap­tive ra­di­a­tions. Their abun­dance and the rel­a­tive ease to cross, raise, and main­tain in the lab make them an ex­cel­lent an­i­mal model for a va­ri­ety of stud­ies. Three­spine stick­le­backs have also served as sub­jects in re­search on en­vi­ron­men­tal ef­fects since they are con­sid­ered bioindi­ca­tors. (Mat­tern, et al., 2007)

  • Positive Impacts
  • research and education

Con­ser­va­tion Sta­tus

The un­ar­mored three­spine stick­le­back, Gas­teros­teus ac­ulea­tus williamsoni, a sub­species found in Cal­i­for­nia, are listed as en­dan­gered in the United States.

Con­trib­u­tors

Susan Wood (au­thor), The Col­lege of New Jer­sey, Keith Pecor (ed­i­tor), The Col­lege of New Jer­sey, Renee Mul­crone (ed­i­tor), Spe­cial Pro­jects.

Glossary

Atlantic Ocean

the body of water between Africa, Europe, the southern ocean (above 60 degrees south latitude), and the western hemisphere. It is the second largest ocean in the world after the Pacific Ocean.

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

Pacific Ocean

body of water between the southern ocean (above 60 degrees south latitude), Australia, Asia, and the western hemisphere. This is the world's largest ocean, covering about 28% of the world's surface.

World Map

Palearctic

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

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.

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

coastal

the nearshore aquatic habitats near a coast, or shoreline.

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

estuarine

an area where a freshwater river meets the ocean and tidal influences result in fluctuations in salinity.

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.

insectivore

An animal that eats mainly insects or spiders.

intertidal or littoral

the area of shoreline influenced mainly by the tides, between the highest and lowest reaches of the tide. An aquatic habitat.

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).

male parental care

parental care is carried out by males

migratory

makes seasonal movements between breeding and wintering grounds

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).

pheromones

chemicals released into air or water that are detected by and responded to by other animals of the same species

planktivore

an animal that mainly eats plankton

polygynous

having more than one female as a mate at one time

saltwater or marine

mainly lives in oceans, seas, or other bodies of salt water.

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.

stores or caches food

places a food item in a special place to be eaten later. Also called "hoarding"

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).

visual

uses sight to communicate

zooplankton

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

Ref­er­ences

Baker, J., S. Fos­ter, M. Bell. 1995. Armor mor­phol­ogy and re­pro­duc­tive out­put in three­spine stick­le­back, Gas­teros­teus ac­ulea­tus. En­vi­ron­men­tal Bi­ol­ogy of Fishes, 44: 225-233.

Bell, M., S. Fos­ter, P. Bowne, D. Buth, T. Haglund, H. Gud­er­ley, R. Woot­ton, J. Baker, F. Who­riskey, G. FitzGer­ald, P. Hart, A. Gill, T. Reim­chen, F. Hunt­ing­ford, P. Wright, J. Tier­ney, W. Row­land, T. Bakker, J. McPhail. 1994. The Evo­lu­tion­ary Bi­ol­ogy of the Three­spine Stick­le­back. New York: Ox­ford Uni­ver­sity Press.

Cresko, W., K. McGuigan, P. Phillips, J. Postleth­wait. 2007. Stud­ies of three­spine stick­le­back de­vel­op­men­tal evo­lu­tion: progress and promise. Ge­net­ica, 129: 105-126.

Day, T., J. Pritchard, D. Schluter. 1994. A com­par­i­son of two stick­le­backs. Evo­lu­tion, 48/5: 1723-1734.

Grand, T. 2000. Risk-tak­ing by three­spine stick­le­back (Gas­teros­teus ac­ulea­tus) pelvic phe­no­types: does mor­phol­ogy pre­dict be­hav­ior?. Be­hav­iour, 137: 889-906.

Hunt­ing­ford, F., P. Wright. 1993. Be­hav­ioral Ecol­ogy of Fishes. Switzer­land: Har­wood Aca­d­e­mic Press.

Marchinko, K. 2008. Pre­da­tion's role in re­peated phe­no­typic and ge­netic di­ver­gence of armor in three­spine stick­le­back. Evo­lu­tion, 63/1: 127-138.

Mat­tern, M., D. Kings­ley, C. Pe­ichel, J. Bough­man, F. Hunt­ing­ford, S. Coyle, S. Ostlund-Nils­son, D. McLen­nan, B. Borg, I. Mayer, M. Pall, I. Bar­ber, I. Kat­si­adaki. 2007. Bi­ol­ogy of the three-spined stick­le­back. Boca Raton: CRC Press.

Messler, A., M. Wund, B. John, S. Fos­ter. 2007. The ef­fects of re­laxed and re­versed se­lec­tion by preda­tors on the an­tipreda­tor be­hav­ior of the three­spine stick­le­back, Gas­teros­teus ac­ulea­tus. Ethol­ogy, 113: 853-863.

Peuhkuri, N. 1998. Shoal com­po­si­tion, body size and for­ag­ing in stick­le­backs. Be­hav­ioral Ecol­ogy and So­cio­bi­ol­ogy, 43: 333-337.

Reim­chen, T. 2000. Preda­tor han­dling fail­ures of lat­eral plate morphs in Gas­teros­teus ac­ulea­tus: func­tional im­pli­ca­tions for the an­ces­tral plate con­di­tion. Be­hav­iour, 137: 1081-1096.

Schluter, D. 1993. Adap­tive ra­di­a­tion in stick­le­backs: size, shape and habi­tat use ef­fi­ciency. Ecol­ogy, 74: 699-799.

Shaw, K., M. Scotti, S. Fos­ter. 2007. An­ces­tral plas­tic­ity and the evo­lu­tion­ary di­ver­si­fi­ca­tion of courtship be­hav­ior in three­spine stick­le­backs. An­i­mal Be­hav­iour, 73: 415-422.

Swarup, H. 1958. Stages in the de­vel­op­ment of the stick­le­back Gas­teros­teus ac­ulea­tus. De­vel­op­ment, 6: 373-383.

Walker, J. 1997. Eco­log­i­cal mor­phol­ogy of la­cus­trine three­spine stick­le­back Gas­teros­teus ac­ulea­tus L. Bi­o­log­i­cal Jour­nal of the Lim­nean So­ci­ety, 61: 3-50.

Ward, A., A. Duff, J. Krause, I. Bar­ber. 2005. Shoal­ing be­hav­iour of stick­le­backs in­fected with the mi­crosporid­ian par­a­site, Glugea anom­ala. En­vi­ron­men­tal Bi­ol­ogy of Fishes, 72/2: 155-160.