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Hypsibarbus wetmorei

Smith, 1931

Formerly Puntius wetmorei Smith, 1931 · Puntius daruphani Smith, 1934 · Barbus beasleyi Fowler, 1937 · Puntius daruphani tweediei Menon, 1954

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Putative adult male individual in the aquarium.
Putative adult male individual in the aquarium.Håkon Haraldseide

Quick facts

Length
250mm SL10in SL
Tank base
240 × 60cm96 × 24in
Temp
20–26°C68–79°F
pH
6.0–8.0
Hardness
not recorded

Difficulty5 of 6 measures

Moderate

More bars, more demanding.

Space
very large tank
Water
tap water
Temp
unfussy
Temperament
unknown
Social
shoal
Compatibility
community tank

H. wetmorei is distinguished from congeners by the following combination of characters: upper body reddish brown; robust body, not compressed; usually 4½ scale rows between lateral line and dorsal-fin origin; 8-12 rakers on first gill arch; 7-9 predorsal scales; 14 circumpeduncular scale rows; usually two scale rows separating vent and anal-fin; <29 lateral line scales; 9-14 serrations on the spinous dorsal-fin ray; distance between distal serrae on posterior margin of last unbranched dorsal-fin ray much greater than the width of their bases.

Etymology

Hypsibarbus: from the Ancient Greek ὕψι (húpsi), and the generic name Barbus, presumably in allusion to the deep body shape in members of this genus.

wetmorei: named in honour of ornithologist Alexander Wetmore (1886-1978), assistant secretary of the Smithsonian Institution, in charge of the United States National Museum.

Distribution

Widespread in mainland Southeast Asia, including the lower Mekong basin in Laos, Thailand, and Cambodia, the Tapi, Chao Phraya and Mae Klong systems in Thailand, and various smaller watersheds in southern Thailand and northern Peninsular Malaysia, as far south as the Pahang River.

Type locality is 'Thailand: Mae Nam Chao Phraya at Chainad'.

Habitat

Displays a preference for flowing water with abundant riparian vegetation, and does not occur in standing waters such as reservoirs or other man-made impoundments.

It is migratory on a seasonal basis, but it is unclear whether the entire population moves upriver to the same spawning sites, or subpopulations undertake shorter migrations.

Aquarium size

Standard length
250mm SL10in SL
Aquarium base
240 × 60cm96 × 24in
Volume
~864litres~228US gal

An aquarium with base dimensions of 240 ∗ 60 cm96 ∗ 24 in or equivalent should be the smallest considered.

Maintenance

Choice of décor is not as critical as water quality and the amount of open swimming-space provided.

However should you possess the means to provide and decorate a sufficiently-sized aquarium for long term care this species would look superb in a set-up designed to resemble a flowing river with a substrate of variably-sized rocks and gravel, some large water-worn boulders and driftwood branches.

Like many other species that hail from running waters it is likely to be intolerant of organic wastes and require spotless water with a high level of dissolved oxygen in order to thrive.

Water conditions

Temperature
20–26°C68–79°F
pH
6.0–8.0
Hardness
not recorded

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Diet

Wild fish are known to feed on shrimps and snails, suggesting a benthic foraging behaviour.

In the aquarium Hypsibarbus spp. are unproblematic feeders but should be offered a varied diet comprising live and frozen foods such as chironomid larvae (bloodworm), Daphnia, and Artemia along with good quality dried flakes, granules and plenty of vegetable matter.

Behaviour and compatibility

Not aggressive unless space is confined, but may eat small fishes and molest slow-moving or timid fishes with its constant activity and vigorous feeding behaviour.

Hypsibarbus are schooling species that should ideally be maintained in groups of half a dozen or more individuals.

Sexual dimorphism

Sexually mature females are likely to be deeper-bodied and may grow larger than males.

Reproduction

Unreported.

Notes

H. wetmorei is distinguished from congeners by the following combination of characters: upper body reddish brown; robust body, not compressed; usually 4½ scale rows between lateral line and dorsal-fin origin; 8-12 rakers on first gill arch; 7-9 predorsal scales; 14 circumpeduncular scale rows; usually two scale rows separating vent and anal-fin; <29 lateral line scales; 9-14 serrations on the spinous dorsal-fin ray; distance between distal serrae on posterior margin of last unbranched dorsal-fin ray much greater than the width of their bases.

H. wetmorei is very similar to H. vernayi, but can be told apart by possessing orange to red (vs. yellow in H. vernayi) pectoral, pelvic, and anal fins. It thus appears likely that yellow-finned fish marketed as H. wetmorei or 'lemon fin barb' in the ornamental trade are actually H. vernayi, with both species are available on a regular basis. The two share a broadly similar geographic distribution, so they may even be collected together.

Hypsibarbus species are valued food fishes throughout their range although most species arre thought to be in decline due to human activity, particularly damming of rivers and agriculture.

The genus is diagnosed as follows: two pairs of barbels; strongly serrated dorsal-fin spine; 8 branched pelvic-fin rays; skin of lower lip discontinuous with lower jaw, separated by a shallow groove; anal-fin base approximately 60% HL; scales with black margins resulting in reticulated appearance; fins often with extended falcate tips; anal and pelvic fins often brightly-coloured.

References

  1. Rainboth, W. J. (1996). The taxonomy, systematics, and zoogeography of Hypsibarbus, a new genus of large barbs (Pisces, Cyprinidae) from the rivers of southeastern Asia. University of California Publications in Zoology v. 129, i-xiii + 1-199
  2. Rainboth, W. J. (1996). FAO species identification field guide for fishery purposes. FAO, Rome, 1-265
  3. 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
  4. Kottelat, M. (2001). Fishes of Laos. WHT Publications, Colombo, 1-198
  5. Smith, H. M. (1931). Descriptions of new genera and species of Siamese fishes. Proceedings of the United States National Museum 79(2873), 1-48

Distribution

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Missing: hardness, a common name, temperament, water condition notes.