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Gymnostomus siamensis

Siamese Mud Carp

Sauvage, 1881

Formerly Morara siamensis Sauvage, 1881 · Tylognathus siamensis de Beaufort, 1927 · Tylognathus brunneus Fowler, 1934 · Tylognathus entmema Fowler, 1934 · Cirrhinus marginipinnis Fowler, 1937 · Cirrhina sauvagei Fang, 1942 · Crossocheilus thai Fowler, 1944

On this page7 sections
Gymnostomus siamensis NP

Quick facts

Length
150mm SL6in SL
Tank base
not recorded
Temp
not recorded
pH
not recorded
Hardness
not recorded

Difficulty3 of 6 measures

Moderate

More bars, more demanding.

Space
large tank
Water
unknown
Temp
unknown
Temperament
unknown
Social
shoal
Compatibility
community tank

G. siamensis can be distinguished from congeners by the following combination of characters: possession of 5½ lateral line scales; body relatively deep, depth fits 3.2-3.4 times in SL; head large and broad, width fits 5.5-6.7 times in SL; snout not or only weakly projecting; body plain silver in colour with no dark marking on caudal peduncle.

Etymology

Gymnostomus: from the Ancient Greek γυμνός (gumnós), meaning 'naked', and στόμα (stóma), meaning 'mouth', presumably in reference to the lack of barbels in this genus.

siamensis: 'from Siam' [Thailand].

Distribution

Recorded from the middle to lower Mekong River basin in Laos, Thailand, Cambodia, and Vietnam, plus the Chao Phraya and Mae Klong watersheds in central and western Thailand.

Type locality is 'Bangkok, Thailand.'

Habitat

Common in the Mekong main channel and larger tributaries, but also recorded in smaller affluents and some impoundments and swamps, especially where aquatic vegetation grows thickly.

During the wet season it moves into inundated zones with standing water to spawn, and is abundant in the massive seasonal migrations of cyprinid fishes that occur in the mainstream Mekong river in December to February and May to July.

Diet

Wild fish are known to feed on periphyton, phytoplankton, and benthic algae.

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Notes

G. siamensis can be distinguished from congeners by the following combination of characters: possession of 5½ lateral line scales; body relatively deep, depth fits 3.2-3.4 times in SL; head large and broad, width fits 5.5-6.7 times in SL; snout not or only weakly projecting; body plain silver in colour with no dark marking on caudal peduncle.

Species currently included in Gymnostomus have previously been placed in a variety of genera including Henicorhynchus, Cirrhinus, Bangana, and Labeo in the last few decades alone. However, Gymnostomus is a senior subjective synonym of Henicorhynchus, thus rendering the latter invalid, while Gymnostomus is easily distinguished from Cirrhinus by possession of 8-9 (vs. 10-15) branched dorsal-fin rays.

Some confusion remains, however, since a recent phylogenetic study (Yang et al., 2012) considered Henicorhynchus to be valid, and members were not recovered in the same evolutionary lineage as Indian Gymnostomus species, suggesting that they are not closely related. It is unclear whether further taxonomic changes will be required in the future in order to reflect this disparity, but here on SF we currently follow Kottelat (2013) since it was published more recently and has been widely accepted, thus Henicorhynchus is a synonym of Gymnostomus.

Gymnostomus species are considered members of the tribe Labeonini within the putative cyprinid subfamily Cyprininae or simply the subfamily Labeoninae (name varies with author). According to the most recent phylogenetic research, this grouping is further divided into four subtribes; Labeoina, Garraina, Osteochilina, and Semilabeoina (Yang et al., 2012). Among these, Gymnostomus is included in the Labeoina alongside Labeo, Bangana sensu stricto (which includes the genus Nukta), Cirrhinus sensu stricto, Cirrhinus microlepis (which is of a different genetic lineage to other Cirrhinus species), and Incisilabeo. As noted above, however, this refers only to the Indian species of Gymnostomus, with the Southeast Asian species placed in the Osteochilina assemblage.

Some Gymnostomus species are common in mainstream rivers at certain times of year and extremely important in local fisheries during these periods.

References

  1. Kottelat, M. (2013). The fishes of the inland waters of southeast Asia: a catalogue and core bibiography of the fishes known to occur in freshwaters, mangroves and estuaries. The Raffles Bulletin of Zoology Supplement 27, 1-663
  2. Kottelat, M. (2003). Nomenclatural status of Crossocheilus burmanicus, C. horai and C. multirastellatus (Osteichthyes: Cyprinidae). Raffles Bulletin of Zoology 51(2), 399-401
  3. Kottelat, M. (2001). Fishes of Laos. WHT Publications, Colombo, 1-198
  4. Rainboth, W. J. (1996). FAO species identification field guide for fishery purposes. Fishes of the Cambodian Mekong. Rome, FAO, 1-265
  5. Roberts, T. R. (1997). Systematic revision of the tropical Asian labeoin cyprinid fish genus Cirrhinus, with descriptions of new species and biological observations on C. lobatus. Natural History Bulletin of the Siam Society 45(2), 171-203
  6. Sauvage, H.-E. (1881). Recherches sur la faune ichthyologique de l'Asie et description d'espèces nouvelles de l'Indo-Chine. Nouvelles Archives du Muséum d'Histoire Naturelle, Paris (Série 2) v. 4, 123-194
  7. Yang, L., M. Arunachalam, T. Sado, B. A. Levin, A. S. Golubtsov, J. Freyhof, J. P. Friel, W-J. Chen, M. V. Hirt, R. Manickam, M. K. Agnew, A. M. Simons, K. Saitoh, M. Miya, R. L. Mayden, and S. He (2012). Molecular phylogeny of the cyprinid tribe Labeonini (Teleostei: Cypriniformes). Molecular Phylogenetics and Evolution 65(2), 362-379

Distribution

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Missing: water parameters, hardness, aquarium size, photograph credits, temperament, aquarium notes, maintenance, water condition notes, behaviour and compatibility, sexual dimorphism, reproduction.