Sternarchogiton nattereri

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Sternarchogiton nattereri
Scientific classification OOjs UI icon edit-ltr.svg
Domain: Eukaryota
Kingdom: Animalia
Phylum: Chordata
Class: Actinopterygii
Order: Gymnotiformes
Family: Apteronotidae
Genus: Sternarchogiton
Species:
S. nattereri
Binomial name
Sternarchogiton nattereri
(Steindachner, 1868)
Synonyms

Oedemognathus exodonMyers, 1936
Sternarchus nattereriSteindachner, 1868

Contents

Sternarchogiton nattereri is a species of weakly electric knifefish in the family Apteronotidae. It is native to the Amazon River system and feeds on sponges. Unlike other members of the genus Sternarchogiton , there is pronounced sexual dimorphism in S. nattereri, with reproductively mature males developing strong external teeth on tips of their jaws. These males are so different from the females and juveniles that they were thought to be a different genus and species, the "tooth-lip knifefish" Oedemognathus exodon, for over 40 years. [1] [2] [3]

Distribution and habitat

S. nattereri is restricted to large river channels in the lowlands of the Amazon basin. Its habitat ranges from high-conductivity, sediment-rich whitewater rivers such as the Rio Solimões, to low-conductivity, sediment-poor blackwaters such as the Rio Negro. It is one of the most common gymnotiforms in Rio Solimões. [1]

Description

S. nattereri has a laterally compressed, knife-shaped body. The dorsal profile of the head is sharply curved from the nape to the snout. The mouth is terminal, with the upper jaw longer than the lower. The dentary is as long as deep, bearing a row of 78 conical teeth on the posterior portion, and there are upper and lower pharyngeal tooth plates bearing 911 and 79 teeth respectively. The eyes are small and covered by translucent skin. The long anal fin contains 180198 rays. The pectoral fins are broad and pointed with 1315 rays each, and the lanceolate caudal fin contains 1115 rays and is almost completely covered with scales. There is a whip-like dorsal appendage anchored into a groove along the back by many fine threads of tendon. [1]

In reproductively mature males, the head becomes elongated and prominent external teeth develop on the upper and lower jaws. Males with teeth tend to have larger gonads than those without. [4] The coloration is a uniform pale white with a pinkish hue caused by subdermal capillaries, especially over anal fin pterygiophores (fin support bones). The operculum is pink due to the presence of the gills underneath. The dorsal surface is gray, with tuberous electroreceptors visible as white dots. All the fins are hyaline, without dark chromatophores. [1] The maximum known length is 25 cm (10 in), [5] with males tending to be larger than females. [4]

Biology and ecology

The diet of S. nattereri consists of freshwater sponges growing on submerged trees, stumps, and other woody debris. [2] Before they were recognized to be the males of S. nattereri, "Oedemognathus exodon" was speculated to use its dentition to feed on fish scales. [6] The external teeth of male S. nattereri are now thought to be used in combat for territory or mates; scars and scratches have been found on the napes of several specimens. [4] [7]

In the Tefé region of Brazil, breeding occurs during the rising water period, with adults spawning in floating meadows along the edges of paraná channels (side branches of whitewater rivers that run through adjacent várzea floodplains). As water levels rise further and dissolved oxygen levels drop, the growing juveniles eventually disperse out of these floodplains within floating rafts of vegetation. [1]

Like other apteronotids, S. nattereri produces a continuous, weak electric field for the purposes of electrolocation and communication; this electric organ discharge (EOD) has a fundamental frequency between 7321465 Hz, one of the largest ranges in the Apteronotidae. The waveform of this discharge has 24 phases and exhibits significant variation amongst individuals, but there is no obvious sexual dimorphism. S. nattereri is additionally able to modulate the frequency and amplitude of its EOD to produce communication signals called "chirps" (short-duration, high-frequency signals) and "gradual frequency rises" (long-duration, low-frequency signals). The frequency elevation of S. nattereri chirps ranges between 50 and 300 Hz above baseline, with a maximum of 500 Hz. [1] [8]

Related Research Articles

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The Gymnotiformes are an order of teleost bony fishes commonly known as Neotropical knifefish or South American knifefish. They have long bodies and swim using undulations of their elongated anal fin. Found almost exclusively in fresh water, these mostly nocturnal fish are capable of producing electric fields to detect prey, for navigation, communication, and, in the case of the electric eel, attack and defense. A few species are familiar to the aquarium trade, such as the black ghost knifefish, the glass knifefish, and the banded knifefish.

<span class="mw-page-title-main">Ghost knifefish</span> Family of fishes

The ghost knifefishes are a family, Apteronotidae, of ray-finned fishes in the order Gymnotiformes. These fish are native to Panama and South America. They inhabit a wide range of freshwater habitats, but more than half the species in the family are found deep in rivers where there is little or no light.

<span class="mw-page-title-main">Electric fish</span> Fish that can generate electric fields

An electric fish is any fish that can generate electric fields. Most electric fish are also electroreceptive, meaning that they can sense electric fields. The only exception is the stargazer family (Uranoscopidae). Electric fish, although a small minority of all fishes, include both oceanic and freshwater species, and both cartilaginous and bony fishes.

<span class="mw-page-title-main">Black ghost knifefish</span> Species of fish

The black ghost knifefish is a tropical fish belonging to the ghost knifefish family (Apteronotidae). They originate in freshwater habitats in South America where they range from Venezuela to the Paraguay–Paraná River, including the Amazon Basin. They are popular in aquaria. The fish is all black except for two white rings on its tail, and a white blaze on its nose, which can occasionally extend into a stripe down its back. It moves mainly by undulating a long fin on its underside. It will grow to a length of 18"-20". Only a fish for those with large aquariums, minimum 100 gallons.

<span class="mw-page-title-main">Rhamphichthyidae</span> Family of fishes

Sand knifefish are freshwater electric fish of the family Rhamphichthyidae, from freshwater habitats in South America.

<span class="mw-page-title-main">Glass knifefish</span> Family of fishes

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<span class="mw-page-title-main">Hypopomidae</span> Family of knifefishes in the order Gymnotiformes

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<i>Magosternarchus</i> Genus of fishes

Magosternarchus is a genus of weakly electric knifefish in the family Apteronotidae, containing two species. They are endemic to Brazil, occurring in large river channels in the Amazon River basin. Both species are unusual benthic predators that specialize in biting off the tails of other knifefishes, and are characterized by their greatly enlarged jaws and teeth. Recent systematic studies indicate that both species should be included in Sternarchella instead of being placed in their own genus.

Sternarchella schotti is a species of weakly electric knifefish in the family Apteronotidae. This species is endemic to Brazil where it is found in the Amazon River basin, and is sometimes kept in aquaria. The species grows to approximately 20 cm in length, and has a pale pink color in life with brown speckling along the dorsal surface of the head and body. As with many other ghost knifefishes (Apteronotidae) this species is aggressive with other electric fish species (Gymnotiformes), but is often compatible in captivity with species in other orders, such as catfish and angelfish. A recommended diet for S. schotti is frozen or live blood worms and insect larva, and diced meat.

Sternarchogiton is a genus of weakly electric knifefish in the family Apteronotidae, with five known species, all living in the main channel of large rivers in the Amazon and Orinoco basins in South America.

<i>Orthosternarchus tamandua</i> Species of fish

Orthosternarchus tamandua, the tamandua knifefish, is a species of weakly electric knifefish in the family Apteronotidae, native to the deep river channels of the Amazon basin. This species is characterized by its whitish-pink color, long tubular snout, long dorsal appendage, and tiny, bilaterally asymmetrical eyes.

Sternarchogiton labiatus is a species of weakly electric knifefish in the family Apteronotidae. Its species name labiatus comes from the Latin labium, meaning "lip", referring to a distinctive three-lobed structure on its lower lips. S. labiatus is only known from the Tefé River, at a depth of 6–14 m (20–46 ft), and from the lower Rio Negro, in the Amazon River basin. They have been captured from both whitewater and blackwater habitats.

Sternarchogiton preto is a species of weakly electric knifefish in the family Apteronotidae. It is native to large river channels and major side branches in the Amazon Basin, and is common in the Tefé River and the Rio Solimões to a depth of 14 m (46 ft). It is found in both whitewater and blackwater habitats. The species name preto comes from the Portuguese word for "black", referring to its coloration.

Sternarchogiton porcinum is a species of weakly electric knifefish in the family Apteronotidae. It is native to deep river channels in the Río Huallaga, Río Napo, and Río Amazonas in Peru, and in the Río Orinoco in Venezuela. Many specimens once identified as S. porcinum from the Brazilian Amazon Basin and the Venezuelan Orinoco are now known to be a different species, S. preto.

<i>Tembeassu marauna</i> Species of fish

Tembeassu marauna is a species of weakly electric knifefish in the family Apteronotidae and the only member of its genus, known only from three specimens collected from the upper Paraná River, Brazil, in 1965. This fish can be identified by fleshy extensions at the tips of its upper and lower jaws, with the upper extension bearing a patch of extra teeth. The function of these unique structures is unknown, but may relate to feeding. Apparently a specialized inhabitant of deep riverine environments, T. marauna may be endangered by extensive dam construction in the upper Paraná region, if not already extinct.

<i>Pariosternarchus</i> Genus of fishes

Pariosternarchus amazonensis is a little-known species of weakly electric knifefish in the family Apteronotidae, and the only member of the genus Pariosternarchus. It is found in the main channel of the Amazon River in Brazil and Peru, likely near the bottom in deep, fast-moving water. This species is characterized by a wide head with a flat bottom, and very large sensory canals along the lower jaw. Like several other knifefishes found in deep river channels, it has reduced eyes, scales, and body pigmentation.

Sternarchella, the bulldog knifefish, is a genus of ghost knifefishes found at depths of 2–50 m (7–164 ft) in the main channel of large rivers in South America. Most are from the Amazon basin, but S. orthos is found both in the Amazon and Orinoco, S. orinoco is restricted to the Orinoco and S. curvioperculata restricted to the upper Paraná basin. They are often common in their habitat.

<i>Rhamphichthys</i> Genus of fishes

Rhamphichthys(Rhamphos = Greek for beak and Ichthys = Greek for fish) is a genus of fish that includes the South American sand knifefish. These fish are eel shaped with a distinct beak like snout which gave them their name. Like most other knifefish Rhamphichthys species have electrical organs that help them live in the murky waters of South America. Currently there are 10 recognized species of Rhamphichthys, although many changes have been made in their taxonomy since their original discovery.

Distocyclus conirostris is a species of glass knifefishes found in the deep waters of the Amazon basin, lower portions of the Potaro River and in major parts of the Rio Orinoco. They are typically relegated to flood basins, flooded forests and main river channels. They have often been found gathering in small groups around vegetation, indicating a social nature. The fish has semi-translucent, glass-like pectoral and anal fins. The main body is a ground-like color with a lighter head. The largest currently recorded specimen is 34.5 cm.

Compsaraia samueli, the pelican knifefish, is a species of apteronotid electric fish from the western Amazon basin of Brazil and Peru. It exhibits pronounced sexual dimorphism in which mature males develop extremely elongated snouts and oral jaws. This phenotype is found in several other apteronotid species and is used in agonistic jaw-locking behaviors between males.

References

  1. 1 2 3 4 5 6 de Santana, C.D.; Crampton, William G. R. (2007). "Revision of The Deep-channel Electric Fish Genus Sternarchogiton (Gymnotiformes: Apteronotidae)". Copeia. 2007 (2): 387–402. doi:10.1643/0045-8511(2007)7[387:ROTDEF]2.0.CO;2.
  2. 1 2 Froese, Rainer, and Daniel Pauly, eds. (2008). "Apteronotidae" in FishBase . December 2008 version.
  3. Lundberg, J. "Freshwater Riches of the Amazon". Natural History. No. September 2001.
  4. 1 2 3 Cox Fernandes, C. & Lundberg, J.G. (2003). "On the sex life of Oedemognathus exodon (Gymnotiformes: Apteronotidae)". Resumos do ASIH. 2003: 124.
  5. Froese, Rainer; Pauly, Daniel (eds.) (2008). "Sternarchogiton nattereri" in FishBase . December 2008 version.
  6. Sazima, I. (1983). "Scale-eating in characoids and other fishes". Environmental Biology of Fishes. 9 (2): 87–101. doi:10.1007/BF00690855.
  7. Campos-da-Paz, R. (2005). "Previously undescribed dental arrangement among electric knifefishes, with comments on the taxonomic and conservation status of Tembeassu marauna Triques (Otophysi: Gymnotiformes: Apteronotidae)". Neotropical Ichthyology. 3 (3): 395–400. doi: 10.1590/s1679-62252005000300007 .
  8. Turner, C.R.; Derylo, M.; de Santana, C.D.; Alves-Gomes, J.A. & Smith, G.T. (Nov 19, 2007). "Phylogenetic comparative analysis of electric communication signals in ghost knifefishes (Gymnotiformes: Apteronotidae)". Journal of Experimental Biology. 210 (Pt 23): 4104–4122. doi: 10.1242/jeb.007930 . PMID   18025011.