Superregnum: Eukaryota
Cladus: Unikonta
Cladus: Opisthokonta
Cladus: Holozoa
Regnum: Animalia
Subregnum: Eumetazoa
Cladus: Bilateria
Cladus: Nephrozoa
Superphylum: Deuterostomia
Phylum: Chordata
Subphylum: Vertebrata
Infraphylum: Gnathostomata
Megaclassis: Osteichthyes
Superclassis/Classis: Actinopterygii
Classis/Subclassis: Actinopteri
Subclassis/Infraclassis: Neopterygii
Infraclassis: Teleostei
Megacohors: Osteoglossocephalai
Supercohors: Clupeocephala
Cohors: Euteleosteomorpha
Subcohors: Neoteleostei
Infracohors: Eurypterygia
Sectio: Ctenosquamata
Subsectio: Acanthomorphata
Divisio/Superordo: Acanthopterygii
Subdivisio: Percomorphaceae
Series: Eupercaria
Ordo: Perciformes
Subordo: Cottoidei
Infraordo: Gasterosteales
Familia: Gasterosteidae
Genera: Apeltes – Culaea – Gasterosteus - Pungitius - Spinachia
Name
Gasterosteidae
References
Nelson, J.S. 2006. Fishes of the World, fourth edition. John Wiley, Hoboken, 624 pp. ISBN 0-471-25031-7. ISBN 978-0-471-25031-9. Reference page.
Vernacular names
català: Gasterosteid
čeština: Koljuškovití
dansk: Hundestejle-familien
Deutsch: Stichlinge
English: Stickleback
eesti: Ogaliklased
Nederlands: Stekelbaarzen
polski: ciernikowate
русский: Колюшковые
The sticklebacks are a family of ray-finned fishes, the Gasterosteidae which have a Holarctic distribution in fresh, brackish and marine waters. They were thought to be related to the pipefish and seahorses but are now thought to be more closely related to the eelpouts and sculpins.
Taxonomy
The stickleback family, Gasterosteidae, was first proposed as a family by the French zoologist Charles Lucien Bonaparte in 1831.[1] It was long thought that the sticklebacks and their relatives made up a suborder, the Gasterosteoidei, of the order Gasterostiformes with the sea horses and pipefishes making up the suborder Syngnathoidei. More recent phylogenetic work has shown that the Gaterosteoidei is more closely related to the Zoarcoidei and the Cottoidei, which means that this taxon would belong in the order Scorpaeniformes.[2] but in other phylogenetic classifications it is treated as the infraorder Gasterosteales within the suborder Cottoidei or as a sister clade to the Zoarcales in the order Zoarciformes.[3]
FishBase recognises 16 species in the family, grouped in five genera.[4] However, several of the species have a number of recognised subspecies, and the taxonomy of the family is thought to be in need of revision.
Genera
The family Gasterosteidae includes the following genera:[4]
Apeltes DeKay, 1842
Culaea Whitley, 1950
Gasterosteus Linnaeus, 1758
Pungitius d'Annone, 1760
Spinachia Cuvier, 1816
Description
1994 Faroe Islands postage stamp with three-spined sticklebacks
Sticklebacks are endemic to the temperate zone[5] and are most commonly found in the ocean, but some can be found in fresh water. The freshwater taxa were trapped in Europe, Asia, and North America after the Ice Age 10,000–20,000 years ago, and have evolved features different from those of the marine species.[6][7]
Sticklebacks are carnivorous, feeding on small animals such as insects, crustaceans and fish larvae.[8][9]
Sticklebacks are characterised by the presence of strong and clearly isolated spines in their dorsal fins.[10] An unusual feature of sticklebacks is that they have no scales, although some species have bony armour plates.
Sizes
The maximum size of the best-known species, the three-spined stickleback (Gasterosteus aculeatus), is about 4 inches, but few of them are more than 3 inches long. They mature sexually at a length of about 2 inches.[11] Most other stickleback species are roughly similar in size or somewhat smaller. The only exception is the far larger fifteen-spined stickleback (Spinachia spinachia), which can reach 22 cm (approx. 8.8 inches).[12] Body form varies with habitat: sticklebacks in shallow lakes have developed a deep body specialized to enable feeding on benthic invertebrates, whilst those in deep oligotrophic lakes have adapted to feed on plankton and have a more slimlined body.[5]
Personality
Research has shown that Sticklebacks display distinct personality traits, specifically in the area of taking a risk, and, can be considered bold or shy. These personality traits were determined to directly influence if they would lead, and if discouraged, attempt to lead again.[13]
Mating
All stickleback species show similar, unusual mating behaviour. Freshwater males develop a red colouration, and although this may be seen in oceanic and benthic species these tend to remain dull-coloured. The male then constructs a nest from weeds held together by spiggin,[5] a kidney secretion, then attract females to the nest. Females signal their readiness to mate with solitary rather than shoaling behaviour, a head-up posture; their bellies are also obviously distended with eggs.[5] Courtship typically involves a zig-zag 'dance' where the male approaches the female in an erratic side-to-side pattern, and dorsal pricking of the female's abdomen.[5] A female lays her eggs inside the nest, where the male fertilises them. The male then guards the eggs until they hatch 7–14 days later (depending on temperature),[5][9] and may continue to guard the fry after they hatch. This large investment in both the nesting site and guarding of the eggs limits the number of females a male can mate with however males spawn multiple times.[5] This introduces the ability for selection to favor male mate choice.[14] Some males die following spawning.[11]
Mating choice
Typically, the sex with the greatest parental investment has the strongest mate preferences.[15] Stickleback species exhibit mutual mate choice in which both the male and female have strong mate preferences. This is due in part to the strong parental investment on behalf of the male in guarding the eggs.[16]
Female mate choice
Female sticklebacks show a strong preference to male stickleback with bright red coloration under their throats. Females mate both more often with males with brighter red coloration and give on average, larger eggs to be fertilized by these males. This preference has led to brighter red coloring.[17][18] This association is possible because the red coloration can only be produced by males that are free of parasites. This is referred to in the Hamilton-Zuk hypothesis.[19]
However, there is also evidence that attractive male red coloration may be a faulty signal of male quality. Male sticklebacks that are more attractive to females due to carotenoid colorants may under-allocate carotenoids to their germline cells.[20] Since carotinoids are beneficial antioxidants, their under-allocation to germline cells can lead to increased oxidative DNA damage to these cells.[20] Therefore, female sticklebacks may risk fertility and the viability of their offspring by choosing redder, but more deteriorated partners with reduced sperm quality.
Female mate choice has also been seen to be condition dependent. Females are almost always the more choosy sex in most species. Female sticklebacks though, have been found to be less choosy of mates when in poor physical condition and inversely, more choosy in good condition.[21]
Male mate choice
In some species, such as the three-spined stickleback, the large investment in both nesting site and guarding of eggs by males limits the number of females a male can mate with.[22] This introduces the ability for selection to favor male mate choice. Male mate choice is rarely studied or observed in many species but multiple studies have confirmed male mate choice within stickleback species. Males show a choosiness similar to females as to what female they are willing to court and mate. Male sticklebacks have been observed to show preference towards female sticklebacks that are larger and longer. This is believed to be because larger females on average produce larger eggs, which leads to a greater offspring survival and fitness.[16] In addition, male sticklebacks have also been observed to prefer females with more distended or bloated stomachs. The benefits of this is also due to larger eggs and thus offspring survival and fitness[23]
Inbreeding avoidance
Female three-spined sticklebacks adjust their courting behaviour to the risk of inbreeding.[24] When gravid females are given the choice between a courting unfamiliar non-sibling and a familiar brother, they prefer to mate with the non-sibling and thus avoid the disadvantages that accompany incest.[24] Eggs from inbred matings compared to eggs from outbred matings have a lower rate of fertilization and hatching, and fewer progeny survive to reproductive age.[24]
Use in science
Niko Tinbergen's studies of the behaviour of this fish were important in the early development of ethology as an example of a fixed action pattern. More recently, the fish have become a favourite system for studying the molecular genetics of evolutionary change in wild populations[25] and a powerful "supermodel" for combining evolutionary studies at molecular, developmental, population genetic, and ecological levels.[26] The nearly complete genome sequence of a reference freshwater stickleback was described in 2012, along with set of genetic variants commonly found in 21 marine and freshwater populations around the world. Some variants, and several chromosome inversions, consistently distinguish marine and freshwater populations, helping identify a genome-wide set of changes contributing to repeated adaptation of sticklebacks to marine and freshwater environments.[27] The adaptations seen in oceanic threespine sticklebacks make them an ideal organism for the study of parallel evolution.[28]
In culture
Monument to the siege stickleback [ru]
There is a sculpture in Kronstadt dedicated to stickleback, which saved thousands of city residents from starvation during the Leningrad Siege of World War II.
References
Richard van der Laan; William N. Eschmeyer & Ronald Fricke (2014). "Family-group names of Recent fishes". Zootaxa. 3882 (2): 001–230. doi:10.11646/zootaxa.3882.1.1. PMID 25543675.
J. S. Nelson; T. C. Grande; M. V. H. Wilson (2016). Fishes of the World (5th ed.). Wiley. pp. 467–495. ISBN 978-1-118-34233-6.
Ricardo Betancur-R; Edward O. Wiley; Gloria Arratia; et al. (2017). "Phylogenetic classification of bony fishes". BMC Evolutionary Biology. 17 (162): 162. Bibcode:2017BMCEE..17..162B. doi:10.1186/s12862-017-0958-3. PMC 5501477. PMID 28683774.
Froese, Rainer; Pauly, Daniel (eds.). "Family Gasterosteidae". FishBase. October 2012 version.
Foster, Susan A.; Cresko, William A.; Johnson, Kevin P.; Tlusty, Michael U.; Willmott, Harleigh E. (1996-01-01). "Patterns of homoplasy in behavioral evolution". In Sanderson, Michael J.; Hufford, Larry (eds.). Homoplasy. Academic Press. pp. 245–269. doi:10.1016/b978-012618030-5/50012-5. ISBN 978-0-12-618030-5. Retrieved 2020-06-04.
Münzing, Joachim (1963). "The evolution of variation and distributional patterns in European populations of the three-spined stickleback, Gasterosteus aculeatus". Evolution. 17 (3): 320–332. doi:10.2307/2406161. JSTOR 2406161.
Bell, Michael A. (1976). "Evolution of phenotypic diversity in Gasterosteus aculeatus superspecies on the Pacific Coast of North America". Systematic Zoology. 25 (3): 211–227. doi:10.2307/2412489. JSTOR 2412489.
The Repeater - NYTimes.com
Orr, James W. & Pietsch, T.W. (1998). Paxton, J.R. & Eschmeyer, W.N. (eds.). Encyclopedia of Fishes. San Diego: Academic Press. pp. 171–172. ISBN 0-12-547665-5.
Colosimo, Pamela F.; Hosemann, Kim E.; Balabhadra, Sarita; Villarreal, Guadalupe; Dickson, Mark; Grimwood, Jane; Schmutz, Jeremy; Myers, Richard M.; Schluter, Dolph; Kingsley, David M. (2005). "Widespread parallel evolution in sticklebacks by repeated fixation of ectodysplasin alleles". Science. 307 (5717): 1928–33. Bibcode:2005Sci...307.1928C. doi:10.1126/science.1107239. PMID 15790847. S2CID 1296135.
"Three-spined stickleback". Gma.org. Retrieved 2012-08-31.
Froese, Rainer; Pauly, Daniel, eds. (2014). "Spinachia spinachia". FishBase.
"Stickleback fish show initiative, personality and leadership". phys.org. Retrieved 2020-06-26.
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Balshine, S.; Kempenaers, B.; Székely, T.; Kokko, H.; Johnstone, R. A. (2002-03-29). "Why is mutual mate choice not the norm? Operational sex ratios, sex roles and the evolution of sexually dimorphic and monomorphic signalling". Philosophical Transactions of the Royal Society of London. Series B: Biological Sciences. 357 (1419): 319–330. doi:10.1098/rstb.2001.0926. PMC 1692955. PMID 11958700.
Kraak, Sarah B. M; Bakker, Theo C. M. (1998-10-01). "Mutual mate choice in sticklebacks: attractive males choose big females, which lay big eggs". Animal Behaviour. 56 (4): 859–866. doi:10.1006/anbe.1998.0822. PMID 9790696. S2CID 21298270.
Barber, Iain; Arnott, Stephen A.; Braithwaite, Victoria A.; Andrew, Jennifer; Huntingford, Felicity A. (2001-01-07). "Indirect fitness consequences of mate choice in sticklebacks: offspring of brighter males grow slowly but resist parasitic infections". Proceedings of the Royal Society of London. Series B: Biological Sciences. 268 (1462): 71–76. doi:10.1098/rspb.2000.1331. PMC 1087602. PMID 12123300.
Bakker, Theo C. M.; Mundwiler, Beat (1994-03-01). "Female mate choice and male red coloration in a natural three-spined stickleback (Gasterosteus aculeatus) population". Behavioral Ecology. 5 (1): 74–80. doi:10.1093/beheco/5.1.74.
Milinski, Manfred; Bakker, Theo C. M. (March 1990). "Female sticklebacks use male coloration in mate choice and hence avoid parasitized males". Nature. 344 (6264): 330–333. Bibcode:1990Natur.344..330M. doi:10.1038/344330a0. S2CID 4322443.
Kim SY, Velando A (January 2020). "Attractive male sticklebacks carry more oxidative DNA damage in the soma and germline". J Evol Biol. 33 (1): 121–6. doi:10.1111/jeb.13552. PMID 31610052.
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Kingsley, D.M.; Peichel, C.L. (2007). "The molecular genetics of evolutionary change in sticklebacks". In Ostlund-Nillson, S.; Mayer, I.; Huntingford, F.A. (eds.). Biology of the three-spine stickleback. CRC Press. pp. 41–81. doi:10.1201/9781420004830-6. ISBN 978-1-4200-0483-0.
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