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Ten Spined Stickleback, Nine Spined Stickleback

Pungitius pungitius (Linnaeus 1758)

Brief Summary

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The ten-spined stickleback has eight to ten spines on its back and three on its belly. The fish is the smallest indigenous fish species of the Netherlands and grows to a maximum of 7 centimeters in length. It lives only one or two years and usually dies after reproducing in its second year of life. Spawning season is from April till July. The male builds a nest in thick overgrowth of waterweed and hornwort. Just like the three-spined stickleback, this fish performs an extensive mating ritual and the males care for the young.
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Diagnostic Description

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Distinguished uniquely from congeners in Europe by having scutes on side of caudal peduncle, forming a keel. Differs further from other members of the genus in Europe by the combination of the following characters: flank lacking scutes; dorsal fin with 7-11 spines; and caudal peduncle wider than deep (Ref. 59043). Distinguished by the presence of 7 to 12 free spines in front of the dorsal fin and a long caudal keel that usually reaches beneath the dorsal fin (Ref. 27547). Dorsal spines separated from one another, each with a rudimentary membrane on its posterior side; anal spine stout and curved; posterior edge of pectorals rounded; pelvic ray pressed close to the spine; caudal fin usually truncate, varying from slightly indented to slightly rounded (Ref. 27547). Pale green, grey, or olive above, strongly pigmented with irregularly arranged dark bars or blotches; silvery below (Ref. 1998). Fins colorless (Ref. 27547). Breeding colors may be variable, depending on sex, population and stage of breeding cycle but color of females always less intense than those of males (Ref. 27547). Aggressive females become dark on the back and paler below, then sometimes become paler with more conspicuous saddle marks as actual breeding approaches (Ref. 30380). Aggressive males become totally black except for the colorless fins and the membranes on the pelvic spines, which are white. At breeding, the males become paler on the back and more intensely black on the belly, especially under the chin (Ref. 28993, 30380). Breeding males on the east coast of North America have been reported as reddish under the head and greenish on the belly (Ref. 27547). Caudal fin with 12 rays (Ref. 2196).
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Recorder
Cristina V. Garilao
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Life Cycle

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During the spawning season, both males and females set up territories which are defended against intruders of either sex. The male builds the nest with plant fragments and binds it together with a kidney secretion. The nest has two openings. The male then entices the female into the nest with quick dancing movements. An enticed female follows the male to his nest, enters it through one opening, deposits 50 to 80 eggs, then leaves through the other opening (Ref. 1998, 27547). In nests with one opening, the female enters, turns around, deposits her eggs and leaves (Ref. 27547). The male then enters the nest and fertilizes the eggs as it swims toward the other opening. More than one female may deposit eggs to the nest. The male guards one opening and aerates the eggs (Ref. 1998). Soon after releasing a clutch of eggs, a female feeds voraciously and in a day or so, is ready to be courted again (Ref. 27547). Sometimes the nest falls apart before the eggs hatch. The male may build a new nest nearby and transfer the eggs to it. At hatching, the male enters the nest to remove egg remains. Newly hatched larvae move to the top of the nest and settle on it. The male may construct a nursery above the nest. As the larvae become more active, the male catches them in his mouth and spits them back to the nest or nursery. As the larvae become more active, the male loses interest in them, and may build a new nest and repeat the process or the breeding season ends (Ref. 28993). Eggs hatch in 6-7 days (Ref. 59043).
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Migration

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Anadromous. Fish that ascend rivers to spawn, as salmon and hilsa do. Sub-division of diadromous. Migrations should be cyclical and predictable and cover more than 100 km.
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Morphology

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Dorsal spines (total): 6 - 12; Dorsal soft rays (total): 9 - 13; Analspines: 1; Analsoft rays: 8 - 13; Vertebrae: 30 - 35
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Trophic Strategy

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Found in shallow vegetated areas of lakes, ponds, and pools of sluggish streams; sometimes in open water over sand (Ref. 5723). Marine populations found near shore and move into freshwater to spawn (Ref. 5723). There appears to be seasonal movements inshore to shallow water in the spring for spawning, and, in the fall, offshore to deep water, or even to the less saline parts of the sea, by the young and adults that survive spawning (Ref. 27547). Nerito-pelagic (Ref. 58426). Feeds on small invertebrates; also on aquatic insects and their eggs and larvae (Ref. 1998). During breeding season, the eggs and larvae are consumed as food (Ref. 1998). It is preyed upon by fish-eating birds, kingfishers and mergansers; fishes such as walleye, brook trout, lake trout, yellow perch and burbot. Parasites of the species include 3 protozoans, 3 myxosporidians, 3 monogeneans, 8 trematodes, 5 cestodes, 6 acanthocephalans, 2 molluscs, 1 branchiuran and 2 copepods (Ref. 5951).
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Biology

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Found in shallow vegetated areas of lakes, ponds, and pools of sluggish streams; sometimes in open water over sand (Ref. 5723). Marine populations found near shore and move into fresh water to spawn (Ref. 5723). There appears to be seasonal movements inshore to shallow water in the spring for spawning, and, in the fall, offshore to deep water, or even to the less saline parts of the sea, by the young and adults that survive spawning (Ref. 27547). Nerito-pelagic (Ref. 58426). Feed on small invertebrates; also on aquatic insects and their eggs and larvae (Ref. 1998). Eggs are found in nests constructed from plant material (Ref. 41678). Males build, guard and aerate the nest where the eggs are deposited (Ref. 205). Females grow faster and live longer than do other males (Ref. 27547). Males seldom live beyond age three, due to heavy post-spawning mortality, but females may live to age five or more (Ref. 27547). When abundant, it is preyed upon by other fishes (Ref. 1998); also preyed by birds (Ref. 27547). May be used as human or dog food or as a source of oil (Ref. 27547).
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Importance

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fisheries: subsistence fisheries; aquarium: commercial
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Ninespine stickleback

provided by wikipedia EN

The ninespine stickleback (Pungitius pungitius), also called the ten-spined stickleback, is a freshwater species of fish in the family Gasterosteidae that inhabits temperate waters. It is widely but locally distributed throughout Eurasia and North America. Despite its name, the number of spines can vary from 8 to 12.

Description

The body of the ninespine stickleback tapers to a very narrow caudal peduncle and the caudal fin is fan-shaped. The body is less deep and more elongated than that of the three-spined stickleback with a thinner and longer caudal peduncle, but the best way of distinguishing these two species is the number of spines in front of the dorsal fin which, for this species, varies from seven to twelve although nine is the commonest number. This species does not have scales but there is a group of small bony plates on the narrowest part of the caudal peduncle at the lateral line. The mouth points upwards in this species. It is generally greyish or olive-brown with silvery flanks irregularly barred or blotched with darker colour.[3] During the breeding season, the males develop a black area around the pelvis and the pelvic spines become white. The eyes are dark with a gold ring around the pupils.

The ninespine stickleback lives in streams, lakes, ponds and rivers and favors thick submerged vegetation, as its small spines do not offer much protection. Like the three spined stickleback, they have a series of scutes or bony plates along the lateral line but, in freshwater populations, these are frequently reduced in number with a gap between the anterior and posterior plates.

Distribution

The species occurs in freshwater systems draining into the Arctic Ocean and the Atlantic across Canada, Alaska, and south to New Jersey. It is present on the North American Pacific coast of Alaska and in the Great Lakes basin. It can also be found throughout most of Eurasia, including the United Kingdom, Greenland, Turkey and the Far East.[1]

Behaviour

During the breeding season (April to July), the male builds a nest suspended on a piece of waterweed, about an inch or so above the substrate at the bottom. The female is attracted by the male and she lays eggs inside the nest, but then departs, leaving parental care to the male. The male guards these eggs and the young fry when they hatch. Then, when they have their spines, he drives them away to look after themselves.

Physiology

The ninespine stickleback is a euryhaline and eurythermal species of teleost fish, occupying both freshwater and marine habitats in higher latitudes of the world. Recently, this species has been under great examination due to pond populations' adaptations of morphology, life history, and behavior which separates them from their marine conspecifics.[4] Many recently isolated populations (<11,000 years) have been studied to identify ranges of phenotypic plasticity and possible genetic drift between populations. It has been found that marine populations exhibit metabolic rate reduction when in colder conditions, in addition to having an elevated hepatosomatic index (HSI) at all temperature conditions as compared to freshwater populations in those same conditions. Hepatosomatic index refers to the proportional size of the liver of the fish to its body mass, as in indication of energy reserves. In addition, certain freshwater pond populations have shown to be able to metabolically compensate to survive a wide range of temperatures, six degrees Celsius to nineteen degrees Celsius. Alterations to metabolic rate, such as decrease in standard metabolic rate, allowed pond population individuals to survive less than favorable conditions. Such physiological differences between populations has not been determined to be exclusively due to plasticity or generic changes; however, there has been found to be significant genetic diversity between marine and freshwater populations.[5]

Due to their climatic versatility, Ninespine Stickleback face much variation in dissolved oxygen in their environment. Ninespines are physoclists, so they lack a connection between their swim bladder and their digestive tract.[6] This means they cannot gulp air from the surface of the water, as physostome fish do, in order to compensate for an environment of low dissolved oxygen, hypoxia. Responses to hypoxia may include increased ventilation rate or slower gill perfusion.[7] Ninespines must rely solely on their gas secretion and absorption abilities, using aquatic surface respiration (ASR) when facing a hypoxic situation. Comparable physostomous fish could prevent ASR to an extent by gulping air, while Ninespines may only rely on only ASR when acclimating to hypoxic conditions. ASR is when the fish rise almost to the surface to ventilate with the top millimeter of water which is high in dissolved oxygen. Ninespine Stickleback do not regularly experience nocturnal hypoxia in their natural environments, and therefore, have slower and decreased control of their swim-bladder lift. Consequently, the Ninespines begin ASR at a much higher dissolved oxygen concentration in hypoxic environments, as compared to other stickleback species, such as the Brook Stickleback.[6]

In culture

The celebrated British zoologist Desmond Morris (born 1928) published a paper in 1952 — "Homosexuality in the ten-spined stickleback (Pygosteus pungitius L.)."[8] — which became the basis of his 1954 doctoral thesis at Oxford University.[9] (This work was undertaken under the tutelage of the famous ethologist Niko Tinbergen.[10]) Morris described and illustrated the normal reproductive behavior of the stickleback as well as certain "pseudofemale" variants which he thought might be fairly frequent in occurrence. ("These observations reveal that the nervous mechanisms of the sexual behavior pattern of the other sex are present, although they are not normally functional.") Although these findings were considered fairly conventional at the time within his specialty, the topic represented a harbinger of the later controversy that Morris's popular publications would arouse when he extended the findings of the biological sciences to the interpretation of aspects of human behavior. He describes some of his adventures with the fish, and his roomful of aquaria, in his book Animal Days (1979).

References

  1. ^ a b NatureServe (2013). "Pungitius pungitius". IUCN Red List of Threatened Species. 2013: e.T18878A18236204. doi:10.2305/IUCN.UK.2013-1.RLTS.T18878A18236204.en. Retrieved 19 November 2021.
  2. ^ Froese, Rainer; Pauly, Daniel (eds.) (2022). "pungitius pungitius" in FishBase. August 2022 version.
  3. ^ "Nine-spined stickleback: Pungitius pungitius". NatureGate. Retrieved 2013-12-15.
  4. ^ Merilä, J (2013). "Nine-spined stickleback (Pungitius pungitius): an emerging model for evolutionary biology research". Annals of the New York Academy of Sciences. 1289 (1): 18–35. Bibcode:2013NYASA1289...18M. doi:10.1111/nyas.12089. PMID 23550583. S2CID 11642528.
  5. ^ Bruneaux M, Nikinmaa M, Laine VN, Lindström K, Primmer CR, Vasemägi A. 2014. Differences in the metabolic response to temperature acclimation in nine-spined stickleback (Pungitius pungitius) populations from contrasting thermal environments. J. Exp. Zool. 321A:550–565
  6. ^ a b Gee, J. H.; Ratynski, R. A. (1988). "Buoyancy regulation during hypoxic stress in sticklebacks (Culaea inconstans, Pungitius pungitius) and the minnow (Pimephales promelas)". Physiological Zoology. 61 (4): 301–311. doi:10.1086/physzool.61.4.30161247. S2CID 87860829.
  7. ^ Willmer, Pat; Stone, Graham; Johnston, Ian (2009). Environmental Physiology of Animals. Retrieved from http://www.eblib.com
  8. ^ Behaviour (1952), 4, 233–261. https://doi.org/10.1163/156853951X00160.
  9. ^ Published as: Morris, D., 1958. "The reproductive behavior of the ten-spined stickleback (Pygosteus pungitius L.).", Behaviour, Supp. 6., 154 pp.
  10. ^ Von Hippel, Frank (editor), Tinbergen's Legacy in Behaviour: Sixty Years of Landmark Stickleback Papers; Leiden/Boston: Brill (2010), iii, 539 p. : ill., maps ; 25 cm.
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Ninespine stickleback: Brief Summary

provided by wikipedia EN

The ninespine stickleback (Pungitius pungitius), also called the ten-spined stickleback, is a freshwater species of fish in the family Gasterosteidae that inhabits temperate waters. It is widely but locally distributed throughout Eurasia and North America. Despite its name, the number of spines can vary from 8 to 12.

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Diet

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Feeds on small invertebrates, aquatic insects and their own eggs and larvae

Reference

North-West Atlantic Ocean species (NWARMS)

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Distribution

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Atlantic drainages across Canada to New Jersey

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North-West Atlantic Ocean species (NWARMS)

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Habitat

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Found in both fresh and salt waters, in shallow, vegetated areas.

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North-West Atlantic Ocean species (NWARMS)

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Habitat

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nektonic

Reference

North-West Atlantic Ocean species (NWARMS)

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