Basin
Golok basin
One river is recorded in the Golok basin, with 9 profiles.
- Species
- 9
- Rivers
- 1
- Photographed
- 9 of 9
- Difficulty rated
- 9 of 9
Rivers in this basinspecies recorded from each
Runs through

Acrochordonichthys rugosusAsian Banjo Catfish
Akysidae · Bleeker, 1846
This is the most commonly-encountered representative of the genus in the aquatic trade though is by no means common. As in other members of the genus body colouration is highly variable, even among individuals collected from a single locality, although a few useful regularities have been observed which can be used to distinguish certain species. This is thought related to the fact that Acrochordonichthys spp. periodically shed their skins and appear paler post-moulting. A. rugosus lends its ...

Akysis hendricksoniHendrickson's Stream Catfish
Akysidae · Alfred, 1966
This species is among the few members of the family to have been exported for the aquarium hobby. It can be differentiated from all other Akysis species by the following combination of characters: head length 17.7-26.5% of standard length (SL); head width 25.4-28.7% SL; body depth at anus 13.0-17.0% SL; caudal peduncle depth 8.1-10.1% SL; interorbital di...

Belontia hasseltiJava Combtail
Osphronemidae · Cuvier, 1831
This species is also referred to by the vernacular name 'Malay combtail'. In terms of external characters it differs most obviously from its only congener, B. signata by its overal brownish grey (vs. reddish) body colouration and presence of a mosaic-type patterning in the unpaired fins (vs. absence). The position of relatedness of the genus Belontia with respect to other anabantoids remains somewhat...

Betta pi
Osphronemidae · Tan, 1998
B. pi is included in the Betta waseri group of closely-related species within the genus, an assemblage within which members share the following combination of characters: base body colouration clay yellow; opercle scales iridescent gold in mature males of all species except B. tomi; throat with black markings which join with black lower jaw in some species; no chin bar.

Homaloptera parclitella
Balitoridae · Tan & Ng, 2005
The water at the type locality is described as 'clear and fast-flowing over a rocky substratum'. H. parclitella was observed in shallow water among the rocks, and sympatric species included Garra cambodgiensis, Neolissochilus soroides, Poropuntius smedleyi, 'Puntius' binotatus, Homaloptera nebulosa and Amblyceps mangois.

Indostomus crocodilus
Indostomidae · Britz & Kottelat, 1999
The type series was collected from a blackwater stream in Toh Daeng Peat swamp forest with the fish found in slow-moving or standing habitats among submerged shoreline roots and leaf litter. In the Tapi River floodplain it was collected from stagnant waters, one of which was an oxbow lake approximately 200 m long and 30 m across at its widest point, surrounded by 'freshwater scrub and swamp trees'. The substrate was composed of mud, woody structures including fallen twigs and branches, and decomposing plant material.

Kryptopterus vitreolusGlass Catfish
Siluridae · Ng & Kottelat, 2013
This species has been available in the trade for decades during which time it's been widely misidentified as the valid congeners K. bicirrhis or, more recently, K. minor. Its identity was not resolved until early 2013 meaning you will find it under one of these two names in the majority of literature published prior to that date. Other trade names include 'Asia...

Puntigrus partipentazona
Cyprinidae · Fowler, 1934
Recorded from numerous river basins in Vietnam, Cambodia, Laos, Thailand, and Peninsular Malaysia, including the Mekong, Chao Phraya, Mae Khlong, Chanthaburi, Tapi, Golok, Terengganu, Pahang, Endau, and Muar. Type locality is 'Kratt, southeastern Siam', which corresponds to modern-day Trat Province, Thailand.

Scleropages formosusAsian Arowana
Osteoglossidae · Müller & Schlegel, 1840
This species is distinguished from its Australian congeners S. jardinii and S. leichardti by possessing a lower number of lateral line scales (21-26 vs 32-36). It occurs naturally in a number of colour forms of which three were elevated to distinct species status in 2003, but the current majority view is that all represent S. formosus pending a detailed review. Kottelat (2013) mentions that the red form may...