Country · Asia
Indonesia
Every profile recorded in Indonesia, native or introduced.
- Species
- 203
- Families
- 30
- Genera
- 77
- Found only here
- 83
- Photographed
- 202 of 203
Where it isAsia
Regions herethe places aquarists name
Shares its fishes withspecies recorded in both
Found only here83
83 of these profiles carry Indonesia and no other country. That is not the same as endemic. Most of these distributions are only half recorded.

Acanthopsoides molobrion
Cobitidae · Siebert, 1991
Acanthopsoides spp. are most closely related to the horse-faced loaches of the genus Acantopsis with which they often co-occur in nature, and thus commonly referred to as 'dwarf horse-face loaches'. The genus currently comprises five species of which four were described by Siebert (1991); these were discovered in existing museum holdings...

Acanthopsoides robertsi
Cobitidae · Siebert, 1991
Acanthopsoides spp. are most closely related to the horse-faced loaches of the genus Acantopsis with which they often co-occur in nature, and thus commonly referred to as 'dwarf horse-face loaches'. Most are very difficult to tell apart but A. robertsi is quite easily identified since it's the only...

Acantopsis dialuzonaHorseface Loach
Cobitidae · van Hasselt, 1823
Juveniles of this 'species' (probably a group of species - see 'distribution') are traded in large numbers but it's still uncommon to see adult specimens in the hobby suggesting their needs are not catered for often enough. This is a shame as when maintained properly they're hardy, long-lived and interesting aquarium residents. Other trade names include 'long-nosed' and 'banana' loach. Please note although certain that more than one species is being tr...

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 ...

Bagrichthys macracanthusBlack Lancer
Bagridae · Bleeker, 1854
The vernacular name 'lancer' is derived from the extended dorsal spine possessed by several members of the genus, which currently contains 7 species. Among them B. macracanthus is most similar to B. majusculus and B. vaillantii but can be told apart from the former by possession of shorter pectoral spines (13.3 - 16.2% SL vs. 15.8 - 20.7%), shorter adipose fin (46.0 - 58.0% SL vs. 38.8 - 45.8%), less deep caudal peduncle (7.1 - 7.5% SL vs. 5.6-7.0%) and larger adult size. From B. vaillantii it di...

Balantiocheilos melanopterusSilver Shark
Cyprinidae · Bleeker, 1850
May also be seen on sale under the trade names 'Bala shark' or 'tricolor shark minnow' and perhaps among the most commonly-encountered ornamental fish species. It is unfortunate that the vast majority of those traded are juveniles and tend to come supplied with little to no information provided regarding their potential size and requirements, a fairly ironic situation given the apparently precarious status of wild populations.

Balitoropsis zollingeri
Balitoridae · Bleeker, 1853
An obligate dweller of swiftly-flowing streams and headwaters containing clear, oxygen-saturated water. It often inhabits riffles and runs and is likely to show a preference for shallower zones. Substrates are generally composed of gravel, rocks, boulders or bedrock carpeted with a rich biofilm formed by algae and other micro-organisms. Juveniles are often found in slower-moving stretches with gravel substrate and submerged tree roots. In both cases patches of aquatic plants are only occasionally pres...

Barbodes banksi
Cyprinidae · Herre, 1940
This species is not often seen in the aquarium hobby but occasionally exported as bycatch among shipments of other fishes. It was described as a subspecies of the closely-related 'P.' binotatus but is currently considered distinct on a tentative basis as per Ng and Tan (1999) who stated it is 'likely' that the two represent extreme colour forms of a single, variably-patterned species.

Barbodes binotatusSpotted Barb
Cyprinidae · Valenciennes, 1842
This species is so ubiquitous across its natural range that it's often referred to simply as 'common barb'. Basic adult colour pattern consists of a small, dark spot at the base of the dorsal-fin origin and another on the caudal peduncle but overall appearance varies somewhat depending on origin, with the anterior dark spot enlarged ventrally forming a bar or posterior spot extending into the caudal-fin, for example. The spots may also appear darker or lighter in some individuals.

Barbodes everetti
Cyprinidae · Boulenger, 1894
This species is uncommon in the aquarium hobby, although the scientific name is widely misapplied to Barbodes dunckeri, a similar-looking species native to Peninsular Malaysia and Singapore commonly referred to as 'clown barb' and labelled as B. everetti in the majority of available literature. The two are quite easy to tell apart, with B. everetti an overall less...

Barbodes kuchingensisFalse Spanner Barb
Cyprinidae · Herre, 1940
This species is rarely-exported for the aquarium hobby but is available on occasion. The name 'P.' kuchingensis is frequently misapplied, however, with subadult forms of 'P.' everetti and some populations of the geographically-variable 'P.' lateristriga regularly traded as such, for example. Though closely-affiliated with and superficially very similar to...

Barbodes lateristrigaSpanner Barb
Cyprinidae · Valenciennes, 1842
This species is commonly-referred to as 'T-barb' in some countries. It's closely-affiliated with and sometimes traded as the congener B. kuchingensis but that species can be told apart by colour pattern comprising a prominent row of dark spots along the lateral line, plus a short, horizontally-orientated streak extending from the upper part of the operculum. In B. lateristriga the lateral markings usually form a solid stripe and there is no streak extending from the operculum.

Barbonymus gonionotus
Cyprinidae · Bleeker, 1849
The genus Barbonymus was erected by Kottelat in 1999 and contains former members of Barbodes from southeast Asia. The type species is B. schwanenfeldii and currently there exist only three other representatives; B. altus, B. collingwoodii and B. gonionotus. The latter two are rare in the hobby although an SF member has kept B. gonionotus in the past so they are worth looking out for if you harbour an...

Barbonymus schwanefeldiiTinfoil barb
Cyprinidae · Bleeker, 1854
This is one of two species traded under the vernacular name 'tinfoil barb', the other being the less well-known congener B. altus. Despite this it appears that B. altus is just as widely available as B. schwanefeldii and in many cases is seen on sale more regularly. Unfortunately both are usually offered at a small size (usually around 50 - 75 mm) with little to no information regarding the eventual size of the fish.

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 albimarginata
Osphronemidae · Kottelat & Ng, 1994
Additonally, fin patterning in B. albimarginata, except the pectoral fins, consists of a broad white distal band, broad dark submarginal band with sharp outer margin and less sharp inner margin, and a plain red inner portion, while in B. channoides the dorsal fin is almost entirely red with only a thin white distal band and the dark submarginal band in the caudal fin does not extend into the uppermost portion of the fin. Base body colouration tends towards a brick-red shade in displaying male B. albimarginata, scarlet in B. channoides (pers. obv.).

Betta antoni
Osphronemidae · Tan & Ng, 2006
The genus Betta is the most speciose within the family Osphronemidae with almost 70 recognised members and looks set to grow further with new ones continuing to be described on a regular basis since the turn of the century. Member species have successfully adapted to inhabit a variety of ecological niches from stagnant ditches to flowing hill streams including some extreme environments such as highly acidic peat swamp forests.

Betta balunga
Osphronemidae · Herre, 1940
Likely to prey on insects and other small invertebrates/zooplankton in nature. Captive fish will normally accept dried products once they're recognised as edible, but should be offered plenty of small live or frozen foods such as Daphnia, Artemia or bloodworm regularly to ensure development of optimal colour and condition. Small insects such as crickets or Drosophila fru...

Betta bellicaSlender Betta
Osphronemidae · Sauvage, 1884
This species lends it name to the B. bellica group/complex of closely-related species within the genus, an assemblage of which members share the following set of characters: long and slender body with dorsal and ventral margins almost parallel; body depth 23-28 % SL; 30-33 anal-fin rays; 11-13 dorsal-fin rays; 32-34 total vertebrae; body dark brown in colour with iridescent green markings on each individual scale.

Betta channoidesSnakehead Betta
Osphronemidae · Kottelat & Ng, 1994
B. channoides and B. albimarginata together comprise the Betta albimarginata group/complex of closely-related species within the genus, these differing from all other members of the genus in colour pattern and by possession of 9-12 anal-fin spines (vs. 0-4). They look very similar to one another but differ in the following characters: anal fin spines 9-11 in B. albimarginata vs. 12 in B. channoides; anal fin rays 21-23 vs. 23-25; lateral scale rows 26-27 vs. 27.5-28; trans...

Betta coccinaScarlet Betta
Osphronemidae · Vierke, 1979
B. coccina can be told apart from other members by the following combination of characters: iridescent green lateral blotch present in male, absent in female; body dark red in colour; no parallel vertical iridescent gold opercle bars; pelvic fin falcate with black filamentous tip, remainder red; median fins with discrete iridescent green spots; dorsal fin-rays 9-12; anal-fin rays 27-29; subdorsal scales 7-8; lateral scales 31-32; predorsal scales 18-21. The genus Betta is the most speciose within the family Osphronemidae with almost 70 reco...

Betta cracens
Osphronemidae · Tan & Ng, 2005
The type locality is a stream in a forest swamp with dense growth of Barclaya motleyi at intervals, part of which had been turned over to cultivation of rubber trees in 1997. The water depth varied between 5-80 cm, pH was 5.8 and syntopic species included 'Puntius' banksi, Rasbora einthoveni, Trigonopoma pauciperforatum, Hemirhamphodon pogonognathus, Betta pugnax, Sphaerichthys osphromenoides, Trichogaster trichopterus, Channa gachua and C. lucius.

Betta dennisyongi
Osphronemidae · Tan, 2013
This species is available in the aquarium hobby but is not traded in large numbers and may have been inadvertently hybridised with the similar-looking congener B. rubra prior to its description since they're typically exported mixed together. It's included in the B. rubra group of closely-related species within the genus, an assemblage erected by Schindler and van der Voort (2012) who...

Betta dimidiata
Osphronemidae · Roberts, 1989
This species is often confused with B. krataios in the aquarium trade, the latter having been known as B. sp. 'Kapuas' prior to description. The two can easily be told apart as the caudal-fin is rounded in B. krataios but spade-shaped and in adults, highly-extended in B. dimidiata. Together these two comprise the B. dimidiata group of closely-related species within the gen...

Betta edithae
Osphronemidae · Vierke, 1984
This species is the only member of the B. edithae group within the genus, and separated from all other Betta spp. by the fact that the branchiostegal membrane and posterior portion of the opercle are opaque or translucent. The original diagnosis by Vierke also states that it has relatively small eyes and short fins with a typical pattern of partial barring.

Betta enisae
Osphronemidae · Kottelat, 1995
This species is included in the B. pugnax complex of closely-related species within the genus, an assemblage of which members are notoriously difficult to tell apart from one another, but which can be characterised collectively by the following set of shared characters: relatively large head measuring 28-40% SL; live colouration usually brown with green or blue iridescent spots; male with similarly-coloured scales on opercle, sometimes extending to abdomen; juveniles and females usually brown with two central body stripes and a dark marking on the caudal peduncle; anal-fin in mature specimens pointed and often elongated; caudal-fin lanceolate.

Betta falx
Osphronemidae · Tan & Kottelat, 1998
B. falx is included in the Betta picta group/complex of closely-related species within the genus, an assemblage comprising species with the following shared characters: unpaired fins rounded (anal-fin sometimes tapering to a blunt point); anal-fin rays I-III, 18-24; dark marginal band on anal and caudal fins, more pronounced in mature males; presence of pre-orbital and post-orbital stripes; presence of chin bar on throat; iridescent green, gold, or blue scales on opercle.

Betta foerschi
Osphronemidae · Vierke, 1979
This species lends its name to the Betta foerschi group of closely-related species within the genus, of which members share the following set of characters: possession of iridescent blue or green unpaired fins; rays and interradial membranes in unpaired fins not contrasting; dorsal fin with thin, bright white distal band; opercle with two, reddish-yellow, vertical bars. Members are regarded as being closely-related to bubble nesting Betta specie...

Betta hendra
Osphronemidae · Schindler & Linke, 2013
This appears to be an undescribed species, and has only been available to the aquarium hobby in limited numbers to date. The rather long-winded trade name derives from the fact that it was initially marketed as two different species, i.e., B. sp. 'Sengalang' and B. sp. 'Palangka'. The spelling of the latter was later corrected but the fish may still be seen with either or both names attached. It looks very similar to fis...

Betta hipposideros
Osphronemidae · Ng & Kottelat, 1994
The easiest way to distinguish these is by examining the throat markings, which vary according to species, and in the case of B. hipposideros form a black horse-shoe shape. It can also be separated from other group members by the following suite of characters: dark blotch on throat joined to black lower lip; presence of transverse bars in dorsal and caudal fins; absence of dark margin in anal-fin; opercle usually with gold scales, without iridescrent green scales; ventral margin of opercle brown; 6.5-7 subdorsal scales (mode 6.5); 9-10 postdorsal scales (mode 9.5); 31-32 lateral scales (mode 32).

Betta ideii
Osphronemidae · Tan & Ng, 2006
Prior to official description this species was traded as B. sp. 'Laut'. It's included in the Betta unimaculata complex of closely-related species within the genus, , of which members share the following set of characters: body long and slender with depth at dorsal fin origin 18-25 % SL; head large and blunt with width 19-24 % SL; long maxilla and lower lip with distance from tip of lower jaw to posterior end of maxilla 27-54 % HL; caudal-fin rounded in sha...

Betta imbellisCrescent Betta
Osphronemidae · Ladiges, 1975
B. imbellis is included in the Betta splendens complex of closely-related species within the genus, of which members share the following set of characters: head length short 22-31 % SL; often a brightly-coloured body; iris of the eye with iridescent green or blue patches; body elongate or slender; opercles parallel when head viewed dorsally; caudal-fin rays red or brown and contrasting with the iridescent interradial membranes; unpaired fins without an irides...

Betta krataios
Osphronemidae · Tan & Ng, 2006
This species was traded as B. sp. 'Kapuas' prior to its formal description and continues to be mislabelled B. dimidiata. The two can easily be told apart as the caudal-fin is rounded in B. krataios but spade-shaped and in adults, highly-extended in B. dimidiata. Together these two comprise the B. dimidiata group/complex of closely-related species within the genus, members of which can be characterised b...

Betta lehi
Osphronemidae · Tan & Ng, 2005
It can be told apart from other members of the B. pugnax group by the following characters: chin bar absent; prsence of transverse bars in the dorsal-fin; no transverse bars in caudal-fin; green iridescent scales present on opercle and body; anal fin with iridescent, light blue distal band; a pair black markings below the postorbital stripe on the opercle of females and juveniles; anal-fin rays 25-29 (mode 28); lateral scales 28-30 (mode 29); postdorsal scales 10-11 (mode 12); pelvic-fin length 34.8-50.6% SL; head length 33.4-36.8% SL; inter-orbital width 31.7-37.4% HL.

Betta mandor
Osphronemidae · Tan & Ng, 2006
This species was known as B. sp. 'Mandor' or B. sp. 'ninja' prior to official description. It belongs to the Betta foerschi group/complex of closely-related species within the genus, of which members share the following set of characters: possession of iridescent blue or green unpaired fins; rays and interradial membranes in unpaired fins not contrasting; dorsal fin with thin, bright white distal band; opercle with two, reddish-yellow, vertical bars. Members are regarded as being closely-related to bubble-nesting Betta species since they share exhibit certain similarities in morp...

Betta midas
Osphronemidae · Tan, 2009
Not recommended for the standard community set-up for reasons already touched upon. It's requirements and disposition mean it's best kept alone or with very peaceful species since much bigger or more vigorous fishes are likely to intimidate and outcompete it. Some small cyprinids and loaches that inhabit similar environments in nature are compat...

Betta miniopinna
Osphronemidae · Tan & Tan, 1994
Bintan has been developed for tourism over the last decades and is heavily-promoted by Indonesia, with luxury beach resorts and golf courses increasing in number. Further deforestation has occurred in order to establish large rubber plantations in the interior of the island. B. miniopinna is now restricted to a few remaining pockets of primary peat swamp forest and has been listed as 'Critically Endangered' on the IUCN Red List of Threatened Species since 1996.

Betta ocellata
Osphronemidae · de Beaufort, 1933
This species is included in the Betta unimaculata complex of closely-related species within the genus, of which members share the following set of characters: body long and slender with depth at dorsal fin origin 18-25 % SL; head large and blunt with width 19-24 % SL; long maxilla and lower lip with distance from tip of lower jaw to posterior end of maxilla 27-54 % HL; caudal-fin rounded in shape, occasionally with elongated median rays; pelvic-fin short and filamentous; dorsal and anal fins relatively pointed.

Betta pardalotos
Osphronemidae · Tan, 2009
This species is included in the Betta waseri group/complex of closely-related species within the genus, an assemblage which also includes a handful of unidentified fishes such as B. sp. 'Medas' on an unofficial basis. Group members share the following combination of characters: base body colouration clay yellow; opercle scales iridescent gold in mature males of all species except ...

Betta patoti
Osphronemidae · Weber & de Beaufort, 1922
This species is included in the Betta unimaculata complex of closely-related species within the genus, of which members share the following set of characters: body long and slender with depth at dorsal fin origin 18-25 % SL; head large and blunt with width 19-24 % SL; long maxilla and lower lip with distance from tip of lower jaw to poste...

Betta pictaSpotted Betta
Osphronemidae · Valenciennes, 1846
This species lends its name to the Betta picta complex of closely-related species, an assemblage of which members share the following combination of characters: unpaired fins rounded (anal fin sometimes pointed): I-III, 18-24 anal-fin rays; anal and caudal fins with dark distal margins, most pronounced in mature males; pre- and post-orbital stripes present; chin bar present; opercle with iridescent blue, green, or gold scales.

Betta pinguis
Osphronemidae · Tan & Kottelat, 1998
B. pinguis is included in the Betta akarensis group/complex of closely-related species within the genus, of which members share the following set of characters: possession of pre-orbital and post-orbital stripes (the post-orbital stripe is faint or interrupted in some species); chin bar present; caudal-fin lanceolate with highly extended median rays in mature males; caudal fin usually with transverse bars; greenish or bluish iridescent scales on body of males in some species; opercle without iridescent scales except in juveniles.

Betta raja
Osphronemidae · Tan & Ng, 2005
It should be noted that not all authors consider the B. pugnax group to contain the same species, with some placed in the B. picta complex by Schindler and Schmidt (2006), for example. B. raja can be told apart from other members of the B. pugnax group by the following characters: mature males with very long pelvic fins covering 15-23 anal-fin rays or even longer than the base of the anal-fin in some cases; anal-fin and lower caudal-fin with black marginal bands; 25-28 anal-fin rays; 30-32 lat...

Betta renata
Osphronemidae · Tan, 1998
This species is included in the Betta waseri group/complex of closely-related species within the genus, an assemblage which also includes a handful of potentially new species such as B. sp. 'Medas' on an unofficial basis. Group 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.

Betta rubra
Osphronemidae · Perugia, 1893
This species was previously included in the Betta foerschi group of closely-related species within the genus, but following its redescription in 2012 now lends its name to the B. rubra group. It was first placed into its own species group by Witte and Schmidt (1992), primarily on the basis of a triangular marking that appears below the eyes of the fish, although Tan and Ng (2005) suggested that this feature is insufficient to warrant the fo...

Betta simorum
Osphronemidae · Tan & Ng, 1996
This species is included in the B. bellica group/complex of closely-related species within the genus, an assemblage of which members share the following set of characters: long and slender body with dorsal and ventral margins almost parallel; body depth 23-28 % SL; 30-33 anal-fin rays; 11-13 dorsal-fin rays; 32-34 total vertebrae; body dark brown in colour with iridescent green markings on each individual scale.

Betta sp. 'Antuta/Bulungan'
Osphronemidae · authority not recorded
This hypothetically-undescribed species appears to be a member of the Betta unimaculata complex of closely-related species within the genus, of which members share the following set of characters: body long and slender with depth at dorsal fin origin 18-25 % SL; head large and blunt with width 19-24 % SL; long maxilla and lower lip with distance from tip of lower jaw to posterior end of maxilla 27-54 % HL; caudal-fin rounded in shape, occasionally with elongated median rays; pelvic-fin short and filamentous; dorsal and anal fins relatively pointed.

Betta spilotogena
Osphronemidae · Ng & Kottelat, 1994
Inhabits freshwater swamps and associated streams, typically shaded from the sun by dense riparian vegetation. The water is normally clear or lightly stained with tannins, and the fish found in water less than a metre deep alongside related species including Betta edithae, B. miniopinna, and B. fusca. PH has been measured to range between 4.9-5.5.

Betta taeniata
Osphronemidae · Regan, 1910
At one locality close to Serian, Sarawak, the habitat comprised a swiftly-flowing, clear hill stream with a substrate of quartz gravel and variably-sized rocks. The pH was 7.0 and there was no aquatic vegetation. The stream was approximately 10 metres across at its widest point and between 5-80 cm deep. B. taeniata was found in sluggish stretches among submerged tree roots, leaf litter, or overhanging riparian vegetation.

Betta uberis
Osphronemidae · Tan & Ng, 2006
The majority of records pertain to an area sandwiched between the lower Arut and Kumai rivers, south of the towns of Pangkalan Bun and Kumai in Kalimantan Tengah (Central Kalimantan) province, Borneo, Indonesia. Addditional collections have taken place in the Sampit river basin to the east, and several hundred kilometres further north in Sukadana district Kalimantan Barat (West Kalimantan) province. Type locality is 'Indonesia: Borneo: Kalimantan Tengah: Arut basin: Pankalanbun', with the specimens having been obtained from the aquarium trade.

Betta unimaculata
Osphronemidae · Popta, 1905
This species is included in the Betta unimaculata complex of closely-related species within the genus, of which members share the following set of characters: body long and slender with depth at dorsal fin origin 18-25 % SL; head large and blunt with width 19-24 % SL; long maxilla and lower lip with distance from tip of lower jaw to posterior end of maxilla 27-54 % HL; caudal-fin rounded in shape, occasionally with elongated median rays; pelvic-fin short and filamentous; dorsal and anal fins relatively pointed.

Boraras brigittaeMosquito Rasbora
Cyprinidae · Vogt, 1978
Appears to be endemic to southwestern Borneo though occurence records are scant. Type locality is 'Bandjarmasin', a port town in the Indonesian province of Kalimantan Selatan (South Kalimantan), and following Kottelat (1991) it's range extends westwards as far as the Jelai Bila river basin, near the town of Sukamara, where it's said to occur sympatrically with the congener B. merah. Boraras was erected in 1993 in order to separa...

Boraras maculatusDwarf Rasbora
Cyprinidae · Duncker, 1904
Within the genus Boraras this species is most similar to B. naevus, though in the latter the red body colouration does not extend into the head. The two also differ in the following characters: anteriormost lateral blotch of comparable size in both sexes in B. maculatus vs. significantly larger in male than female B. naevus; 9-10 + 9 principal caudal-fin rays vs. 9 + 8; 26-29 lateral scales vs. 24-26; i.6.i. pelvic-fin rays vs. i.5.i.

Boraras merah
Cyprinidae · Kottelat, 1991
Appears endemic to southern Borneo. The type specimens were collected from the Jelai Bila river basin at Nataik Sedawak, presumably a settlement of some kind, near the town of Sukamara in the Indonesian province of Kalimantan Tengah (Central Kalimantan). Its range extends westwards from the Jelai Bila watershed whereas that of the congener B. brigittae, with which it may occur sympatrically there (see 'Notes'), extends east.

Brachydanio albolineataPearl 'Danio'
Cyprinidae · Blyth, 1860
Doubts remain whether B. albolineata is representative of a single species or a group of similarly-patterned, closely-related fish, and the form from Chantaburi province in eastern Thailand was revalidated as B. pulchra (formerly Danio pulcher Smith, 1931) by Kottelat (2013). The status of the currently invalid Danio tweedei (Brittan, 1955) from Kedah state, northern Peninsular Malaysia may also be in question, since fish from that area are clearly...

Brachygobius doriaeBumblebee Goby
Gobiidae · Günther, 1868
This species is among the more frequently-traded members of the genus, although confusion regarding its identification and natural distribution is commonplace and it's often misidentified as B. nunus or B. xanthozonus. It can be diagnosed as follows: <30 lateral scales; one black band on head, three on body; first black band on body overlapping first dorsal fin to the extent that almost all fin, except a narrow margin, is black, and beginning opposite centre of opercle...

Brevibora cheeya
Cyprinidae · Liao & Tan, 2011
This species is very rare in the trade and is normally imported only as bycatch among shipments of other fishes. It can be told apart from its well-known congener B. dorsiocellata by a combination of characters as follows: lateral line complete (25-30 pored scales vs. 4-9); more scales in the lateral row (29-32 vs. 25-27); larger adult siz...

Brevibora dorsiocellataEyespot Rasbora
Cyprinidae · Duncker, 1904
B. dorsiocellata is sometimes traded as 'green-eyed', 'emerald-eyed' or 'hi-spot' rasbora. There appear to exist several geographical forms of the species at least two of which have been seen in the trade. The most common is the rather plain-coloured fish that is produced commercially in large numbers and has gained popularity due to the bright green/blue reflective patch in the lower part of the eye.

Butis amboinensisOlive Flathead Gudgeon
Eleotridae · Bleeker, 1853
This species is not traded for aquaria but is occasionally exported as bycatch among shipments of other species. It differs from congeners in that the outermost row of teeth are not enlarged plus the interorbital space and cheek below eye are not scaled. Butis spp. are largely nocturnal ambush predators with cryptic...

Carinotetraodon irrubescoRed-tailed Redeye Puffer
Tetraodontidae · Tan, 1999
This species is uncommon in the aquarium hobby. It is similar to the congeners C. borneensis and C. lorteti but can be told apart by males possessing a red (vs. bluish to greyish with black and white distal bands in C. lorteti) caudal-fin and lacking (vs. possessing) a black blotch at the base of the dorsal-fin.

Channa gachuaDwarf Snakehead
Channidae · Hamilton, 1822
Generally considered to have an enormous natural range extending from Iran to Taiwan and Bali, with records existing from Iran, Iraq, Afghanistan, Pakistan, Nepal, India, Sri Lanka, Bangladesh, Bhutan, China, Myanmar, Thailand, Laos, Cambodia, Vietnam, Malaysia, Indonesia, and Singapore. However there exists significant evidence to suggest that C. gachua as currently understood represents a complex of similar-looking species, and a taxonomic review of the group is clearly required.

Channa luciusForest Snakehead
Channidae · Cuvier, 1831
Prefers a dimly-lit aquarium with plenty of cover in the form of live plants, driftwood branches, terracotta pipes, plant pots, etc., arranged to form a network of nooks, crannies, and shaded spots. Surface vegetation such as Ceratopteris spp. is also appreciated and makes the fish less inclined to conceal themselves.

Channa melasomaBlack Snakehead
Channidae · Bleeker, 1851
This species can be told apart from the similar-looking congener C. baramensis (once considered synonymous with C. melasoma) by absence (vs. presence) of a black spot in the centre of numerous body scales and absence (vs. presence in specimens larger than 120 mm SL) of a barred caudal-fin pattern.

Channa pleuropthalmaOcellated Snakehead
Channidae · Bleeker, 1851
Channa pleuropthalma

Chromobotia macracanthusClown Loach
Botiidae · Bleeker, 1852
This species is arguably one of the most misunderstood in the hobby since it's wholly unsuitable for smaller aquaria despite its ubiquitous availability. Most retailers sell it without providing what should be considered essential information regarding long-term care and most specimens undoubtedly fail to reach their potential in captivity. The purchase of a group is also a considerable investment given that if properly cared for typical life span is in excess...

Crossocheilus langeiSiamese Algae Eater
Cyprinidae · Bleeker, 1860
C. oblongus is another name widely misused in the trade but that species has seemingly never been exported and was described as a blueish fish with yellow fins. It's native to streams of Gunung Salak mountain in Bogor Regency, West Java, Indonesia where collecting of ornamental fishes is almost non-existent. Other species of laterally-striped Crossocheilus also exist and may be available from time-to-time but are more easily told apart from the group described above.

Crossocheilus nigriloba
Cyprinidae · Popta, 1904
While separating some of the fish that may be found on sale as 'C. siamensis' is a tricky task, C. nigriloba is quite simple to identify. The dark lateral body stripe uniquely breaks up into a series of blotches when the fish are sparring, stressed or sleeping and the lower caudal fin lobe contains dark pigmentation suffused with red. The latter feature has given rise to the trade name of 'penguin flying fox'.

Cyclocheilichthys apogonBeardless Barb
Cyprinidae · Valenciennes, 1842
In the aquarium trade this species may also be seen on sale as 'skinhead barb'. As with others in the genus little has been written regarding its captive care but it makes a peaceful and unusual addition to larger aquaria. The best way of obtaining it may be to keep an eye on shipments of wild fishes from Indochina and the Greater Sunda Islands as it's rarely imported in large numbers and most often arrives as bycatch.

Cyclocheilichthys armatus
Cyprinidae · Valenciennes, 1842
It can be distinguished from congeners by possessing one or two pairs of barbels, a black blotch at the base of the caudal-fin, and rows of dark spots along the lateral scale rows. Members of Cyclocheilichthys are characterised by possessing a serrated dorsal fin spine, 9 branched pelvic fin rays, a conical snout, small, subterminal...

Cyclocheilichthys heteronema
Cyprinidae · Bleeker, 1854
This species is currently understood to have a considerable natural range extending eastwards from Myanmar via Thailand, Laos, Cambodia as far as Vietnam and to the south through Peninsular Malaysia and into the Greater Sunda Islands of Borneo and Sumatra. It thus occurs in the Mekong, Mae Klong and Chao Phraya drainages as well as a host of other river basins, lakes and reservoirs including the Tonlé Sap river...

Cyclocheilichthys janthochir
Cyprinidae · Bleeker, 1854
In the exceptionally diverse Danau Sentarum lake system of the upper Kapuas River basin, West Kalimantan, sympatric species include Scleropages formosus, Barbonymus gonionotus, B. schwanenfeldii, Crossocheilus nigriloba, Cyclocheilichthys apogon, C. repasson, Epalzeorhynchos kalopterus, Labiobarbus ocellatus , Leptobarbus hoevenii, Luciosoma spilopleura plus various representatives of Barbodes, Rasbora and Osteochilus.

Cyclocheilichthys repasson
Cyprinidae · Bleeker, 1853
An ideal resident of the larger, well-furnished community set-up though it might upset slow-moving or timid companions simply by its size. There are plenty of suitable tankmates including many cyprinids, loaches, cichlids, catfish and characins, but as always when selecting a compatible community of fish proper research is essential. A community based around one of its native countries or river basins...

Datnioides polotaSilver Tiger Perch
Datnioididae · Hamilton, 1822
D. polota is sometimes referred to as D. quadrifasciatus (Sevastianov, 1809) but the original name of the latter, Chaetodon quadrifasciatus Sevastianov, 1809, is a junior primary homonym of the older Chaetodon quadrifasciatus Bloch & Schneider 1801, thus Coius polota Hamilton, 1822 takes precedence.

Desmopuntius endecanalis
Cyprinidae · Roberts, 1989
Probably a micropredator feeding on small insects, worms, crustaceans and other zooplankton in nature. In the aquarium it will accept dried foods of a suitable size but should not be fed these exclusively. Daily meals of small live and frozen fare such as Daphnia, Artemia, and suchlike will result in the best colouration and encourage the fish to come into breeding condition. It's a schooling species by natur...

Desmopuntius foerschi
Cyprinidae · Kottelat, 1982
D. foerschi is sometimes traded as 'boomerang barb' or 'Foersch's fire barb' and is included in a group of closely-related, similar-looking fishes which were moved into the new genus Desmopuntius by Kottelat (2013). It can be told apart from other vertically-striped congeners by possession of additional dark blotches between the second, third and fourth vertical bars and a further marking at the posterior base o...

Desmopuntius gemellus
Cyprinidae · Kottelat, 1996
The type series was purchased from a market in Jambi province, eastern Sumatra, Indonesia and this species is also known from neighbouring Riau province plus the island province of Bangka. On Sumatra it may be restricted to the Indragiri and Batang Hari river systems. Inhabits peat swamp forests and associated black water streams in which the water is typically stained brown with humic acids and other chemicals released by decaying organic material. The dissolved mineral content is generally negligible and the pH can be as...

Desmopuntius hexazona'Pentazona' Barb
Cyprinidae · Weber & de Beaufort, 1912
Native to parts of southern Borneo, eastern Sumatra, Singapore, and the Malay Peninsula. In Singapore it's considered highly-endangered and is now restricted to the Central Catchment nature reserve. Type locality is 'Tuluk and Gunung Sahilan, Sumatra, Indonesia' which appears to correspond to localities within the Kampar River drainage of which the former is now known as Teluk Meranti and is o...

Desmopuntius johorensisStriped Barb
Cyprinidae · Duncker, 1904
D. johorensis can be distinguished by the following combination of characters: 5-6 dark, lateral stripes on body in specimens larger than 40 mm; stripes immediately above and below the central stripe (stripes '+1' and '-1', respectively) located on scale rows +2 and -2, not touching dorsal and ventral midlines (except in some small specimens from Peninsular Malaysia); stripes broad, typically between 0.5-1 scale rows deep...

Desmopuntius rhomboocellatusSnakeskin Barb
Cyprinidae · Koumans, 1940
Endemic to southern Kalimantan, the Indonesian portion of Borneo where it's been recorded from several river systems including the Kapuas, Kepayang, Barito and Kahajan. Type locality is given as 'Canal along the highway from Oelin to Bandjermasin, about 15 kilometers from Bandjermasin, Borneo.' Often referred to as the 'rhomb' or 'rhombo' barb and included in a group of closely-related, similar-looking congeners which also includes...

Desmopuntius trifasciatus
Cyprinidae · Kottelat, 1996
This species is one of three similar-looking members of the genus alongside D. johorensis and D. trifasciatus, while it may also be confused with Striuntius lineatus. Juveniles of all except S. lineatus exhibit a vertically-barred rather than laterally-striped colour pattern, the metamorphosis to adult patterning beginning at around 20 mm SL and normally being complete by 30-40 mm.

Eirmotus insignis
Cyprinidae · Tan & Kottelat, 2008
Typically inhabits slow-moving, shallow, shady rainforest streams and swamps with dense submerged and marginal vegetation. The conditions are often rather turbid and the substrate composed of mud or fallen leaves, twigs and branches. Such environments characteristically contain soft, weakly acidic water and are often dimly-lit due to the rainforest canopy above. The fish are found sheltering among overhanging tree roots and aquatic vegetation.

Epalzeorhynchos kalopterumFlying Fox
Cyprinidae · Bleeker, 1850
Confusion with similar-looking fishes from other genera, such as Garra cambodgiensis, laterally-striped Crossocheilus spp. or Gyrinocheilus aymonieri is not uncommon, and are largely attributable to the use of trade names such as 'false flying fox' or 'Siamese flying fox'. When compared with the other species E. kalopterus exhibits several unique characters but perhaps the simplest way to identify it is by the characteristic white-edged, red and black coloured fins and the presence of two pairs of barbels.

Gastromyzon ctenocephalus
Gastromyzontidae · Roberts, 1982
One of the more commonly-traded members of the genus and often found in mixed shipments which may contain other Gastromyzon spp. or related fishes like Beaufortia kweichowensis, these often labelled collectively as 'Borneo sucker', 'Hong Kong pleco', 'butterfly loach', etc. It's sometimes misidentified as G. punctulatus, a species not currently traded which possesses yellow finnage and a lighter-coloured, less-intensely spotted body.

Gastromyzon lepidogaster
Gastromyzontidae · Roberts, 1982
This species is variable in terms of colour. Large adults may be bright green, orange or barred but are apparently capable of changing from barred to plain in just a few seconds. These different forms have been recorded in the same natural habitats, and some individuals also possess prominent nuptial tubercules covering much of the body.

Gastromyzon sp. 'SK01'
Gastromyzontidae · authority not recorded
This undescribed species has probably not been seen in the aquarium trade yet but is occasionally maintained private collectors. The 'SK' numbering system used here refers to 'South Kalimantan', home to several unidentified members of the genus. Gastromyzon spp. are placed into various 'species groups' (artificial assemblages of species which may or may not be monophyletic) for ease of reference, and based on colour and patterning G. sp. 'SK01' appears similar to members of the G. ridens group which also includes G. crenastus, G. stellatus and G. zebrinus.

Gastromyzon sp. 'SK02'
Gastromyzontidae · authority not recorded
Known only from headwaters of the Sungai (river) Amandit, a tributary of the larger Barito basin in the Meratus mountain range, Kalimantan Selatan (South Kalimantan) province, Indonesian Borneo. There currently exist 36 officially-described members of the genus, all of which are endemic to the island with over half restricted to a single river basin or sub-basin.

Gastromyzon sp. 'SK03'
Gastromyzontidae · authority not recorded
Gastromyzon spp. are obligate dwellers of swift, shallow streams containing clear, oxygen-saturated water and have been recorded from sea level to 1350 m amsl throughout hill regions of Borneo. They typically inhabit riffles and runs and are often found above or below cascades and waterfalls. Substrates are generally composed of gravel, rocks, boulders or bedrock carpeted with a rich biofilm formed by algae and other micro-organisms.

Gastromyzon zebrinus
Gastromyzontidae · Tan, 2006
Much of the natural diet is likely to be composed of benthic algae plus associated micro-organisms which are rasped from solid surfaces. In captivity it will accept good-quality dried foods and meatier items like live or frozen bloodworm but may suffer internal problems if the diet contains excessive protein. Home-made foods usi...

Gymnochanda filamentosa
Ambassidae · Fraser-Brunner, 1955
G. filamentosa has appeared in the ornamental trade but is evidently delicate and therefore recommended only to experienced aquarists. It can be told apart from congeners by the following combination of characters: possession of filamentous dorsal and anal-fin rays in males; body transparent to translucent yellowish-brown colour in life; absence of a highly-extended second anal-fin spine; absence of carmine-red pigmentation in the dorsal, anal an...

Gymnochanda verae
Ambassidae · Tan & Lim, 2011
A densely-planted tank with floating vegetation and roots, twigs or branches and natural leaf litter would seem appropriate. There's no need to use natural peat, the collection of which is both unsustainable and environmentally-destructive. Filtration should not be strong with an air-powered sponge-type unit ideal, and given it naturally inhab...

Gymnothorax tile'Freshwater' Moray Eel
Muraenidae · Hamilton, 1822
Gymnothorax tile

Helostoma temminkiiKissing Gourami
Helostomatidae · Cuvier, 1829
The pinkish-white form of this species is among the most widely-traded aquarium fishes in the world but does not occur naturally and is in fact a leucistic variant bred specifically for ornamental purposes. The 'short-bodied' or 'balloon' variety also continues to be fashionable but under no circumstances do we recommend the purchase of these intentionally disfigured animals which tend to have much shorter life spans than the naturally-shaped fish. There also exists a less-po...

Homaloptera orthogoniataSaddle-back Loach
Balitoridae · Vaillant, 1902
This species appears is rare in the aquarium hobby with the majority of images both online and in the published literature instead depicting H. confuzona or H. parclitella. All three are members of the H. ocellata 'group' within the genus which currently contains H. ocellata, H. bilineata, H. confuzona, H. orthogoniata, H. ogilviei and H. parclitella. Following Tan and Ng (2005) these share possession of...

Homalopteroides nebulosus
Balitoridae · Alfred, 1969
The genus Homalopteroides was revalidated by Randall and Page (2012) and is told apart from the related Homaloptera by the following character combination: dorsal-fin origin above pelvic-fin; ≤ 60 lateral-line scales; ≤ 30 predorsal scales; oral morphology consisting of two thin and widely separated rostral barbels on each side of the mouth, thin crescent-shaped lips, the absence of any structure such as a mental pad or lobes between the lateral portions of the lower lip, and a chin that extends anterior to the lateral portions of the lower lip.

Homalopteroides stephensoni
Balitoridae · Hora, 1932
Tan (2009) redescribed H. stephensoni and it possesses the following unique character set: sub-inferior mouth with thin barbels; five principle, 12-13 secondary pectoral fin rays (usually 12); scaleless belly; pattern of keeled scales on anterior, dorsal portion of body consisting of a single central keel in the posterior third of each scale; 43-50 lateral line...

Homalopteroides tweediei
Balitoridae · Herre, 1940
Described from Kota Tinggi district, Johor state, Peninsular Malaysia but since recorded throughout much of the country as well as parts of the the Mekong river system in Thailand, Laos, Cambodia and Vietnam plus the Kapuas and several other river basins in Kalimantan Barat (West Kalimantan) province, Indonesian Borneo. In the Kahang River, part of the Endau drainage in Jo...

Homalopterula gymnogaster
Balitoridae · Bleeker, 1853
Type locality is given as 'Lake Meninju, Sumatra, Indonesia', currently known as Danau (lake) Maninjau, but conceivably the fish may have been obtained from the outflowing Antokan river rather on its western side than the lake itself.
Homalopterula ripleyi
Balitoridae · Fowler, 1940
Fowler (1940) described this species as the unique member of his new genus Homalopterula on the basis of a single specimen, separated from related genera by the curved shape of the jaws, truncate caudal-fin and scaleless ventral surface.

Hypergastromyzon humilis
Gastromyzontidae · Roberts, 1989
The differences in pelvic-fin structure and gill openings led Roberts to redefine the genus when describing H. eubranchus, whereas Tan (2006) expressed doubts that the two are even congeneric but was unable to reach a definitive conclusion in the absence of fresh material. At any rate both species can be easily differentiated from Gastromyzon and Neogastromyzon spp. by observing the mo...

Hypseleotris compressaEmpire Gudgeon
Eleotridae · Krefft, 1864
Occurs in northern and eastern Australia and southern New Guinea. In the former its range extends from the Pilbara and Kimberley regions of Western Australia state around the northern and eastern coastlines of the continent as far as the Towamba river system in New South Wales state.

Iriatherina werneriThreadfin Rainbowfish
Melanotaeniidae · Meinken, 1974
There also exists a sister-group relationship between the Melanotaeniidae and Malagasy family Bedotiidae, which may seem surprising given their respective modern-day distributional patterns. The precise origin and subsequent dispersal of the two families has been the subject of debate, with some palentologists suggesting that Madagascar's freshwater fishes derived froma trans-oceanic dispersal during the Cenozoic Era, but the most compelling arguments currently indicate a freshwater radiation which occurred during the Mezozoic break-up of Gondwana.

Kottelatia brittani
Cyprinidae · Axelrod, 1976
This species was described from 'Johore River, Segamat, Malaysia', which corresponds to Segamat District within the the Johor River watershed, Johor state, southern Peninsular Malaysia, but the type specimens were obtained via a Singapore wholesaler so it's possible that a mistake was made as there exist no other records of the species in Peninsular Malaysia. It's also been recorded from the Kapuas drainage...

Kottelatlimia hipporhynchos
Cobitidae · Kottelat & Tan, 2008
This species differs from congeners in the presence of papillae covering the mouthparts (lips, barbels, and lobes) which are absent in other species. It's also the largest species in the genus and the serrae on the second pectoral fin rays in males form a broa...

Kottelatlimia pristes
Cobitidae · Roberts, 1989
The genus Kottelatlimia was erected by Nalbant (1994) to accommodate K. katik which had previously been assigned to Lepidocephalichthys but differs in various aspects noted earlier by Kottelat and Lim (1992) including: relatively small adult size; scaleless...

Kryptopterus bicirrhis
Siluridae · Valenciennes, 1840
Generally peaceful though it may predate on smaller fishes and is somewhat timid so does not compete well with much larger, robust or otherwise boisterous species. Peaceful, comparably-sized cyprinids, loaches and other catfishes perhaps constitute the best options but be sure to research your choices thoroughly prior to purchase.

Kryptopterus cryptopterusBlue Sheatfish
Siluridae · Bleeker, 1851
Known from the Malay Peninsula and Singapore plus Greater Sunda Islands of Sumatra, Borneo and Java in Indonesia with populati0ns from Thailand, Cambodia, Laos and Vietnam formerly considered as conspecific now referred to K. geminus (Ng, 2003). Type locality is given as 'Bandjarmassing' which corresponds to a town now more commonly referred to as 'Banjarmasin' in South Kalimantan (Kalimantan Selatan) province, Indonesia (Borneo).

Kryptopterus limpok
Siluridae · Bleeker, 1852
Type locality is 'Palembang, Sumatra, Indonesia', but this species is widely-distributed throughout much of Southeast Asia including major river systems in Thailand, Laos, Cambodia, Vietnam and Peninsular Malaysia plus the Greater Sunda Islands of Sumatra, Borneo and Java. It's been extensively recorded from the Mekong, Cha...

Kryptopterus macrocephalusStriped Glass Catfish
Siluridae · Bleeker, 1858
Has been recorded in fast-flowing environments but most commonly associated with peat swamp forests and associated blackwater streams. Many such habitats have suffered degradation of some kind but in unaltered cases the dense canopy of branches above means very little light penetrates the surface of such environments, and riparian vegetation also tends to grow thickly.

Kryptopterus palembangensis
Siluridae · Bleeker, 1852
This species is almost unheard of in the aquarium trade though may occasionally be exported among shipments of wild fishes from Sumatra. It's closely-related to K. bichirris but is told apart by presence (vs. absence) of a prominent, dark lateral stripe on each flank. Kryptopterus species are found only in Southeast Asia and the genus has been consi...

Labiobarbus leptocheilus
Cyprinidae · Valenciennes, 1842
Different populations vary in appearance somewhat (see image of Salween specimen for example), and L. leptocheilus may turn out to represent a group of closely-related species rather than a single taxon. The population from the Cambodian Mekong has been considered to represent a distinct species, Labiobarbus lineatus, although that name is currently a synonym of L. leptocheilus following Kottelat (2013). It is widely used in the ornamental trade, however.

Labiobarbus ocellatus
Cyprinidae · Heckel, 1843
It can be distinguished from congeners by the following combination of characters: 61-68 scales in the lateral series; a small, well-defined, sometimes ocellated black spot on the shoulder and another in the centre of the caudal peduncle; body without longitudinal stripes formed by spots on scales; caudal fin uniformly dusky or colourless, lobes without stripes or black margins.

Lepidocephalichthys furcatus
Cobitidae · de Beaufort, 1933
This species is not traded often but is occasionally available as bycatch among shipments of other species. It can be told apart from congeners most easily by the prominent, dorsally-orientated, roughly semi-circular lamina circularis in males, a feature unique within the genus. Other distinguishing characters include a combination of: forked caudal-fin; relatively small adult size; dark <-shaped mark at the base of the caudal-fin; a black spot at the base of branched caudal-fin rays 3-5.

Lepidocephalichthys hasselti
Cobitidae · Valenciennes, 1846
At one locality close to Ban Na Hwai, Chiang Mai Province, Thailand L. hasselti was collected from a shallow (<0.5 m) pool in a swampy zone between forest and rice fields. The substrate was of mud, there was no aquatic vegetation and it was being used as drinking water by local animals, with the only effluent connected to a 'small creek'. Other species found there were Physoschistura pseudobrunneana, Rasbora hobelmani and Systomus cf. orphoides.

Lepidocephalichthys tomaculum
Cobitidae · Kottelat & Lim, 1992
This species is not traded often but may be available occasionally bycatch among shipments of other species. It can be told apart from congeners most easily by the following combination of characters: truncate caudal-fin; scaleless patch on top of head; caudal-fin with reticulated patterning, sometimes appearing as a series of thin vertical bars; body reddish brown with darker markings; 3-7 predorsal and 3-6 postdorsal thin, transverse dark bars running across the dorsal surface; relatively deep...

Lepidocephalus macrochir
Cobitidae · Bleeker, 1854
The distribution records for this species are somewhat confusing. It was described from the confluence of the Lamatang and Enim rivers, Palambang Province, Sumatra and has since been recorded from Thailand (Chao Phraya River), Peninsular Malaysia (Pahang River) plus the islands of Java (Solo River) and Borneo (Kapuas and Barito rivers).

Luciosoma setigerumApollo Shark
Cyprinidae · Valenciennes, 1842
There is a fish of unknown geographical origin which matches the majority of diagnostic features for L. setigerum with the exception that the dark lateral stripe is absent in the anterior portion of the body and is not composed of interconnected spots. It is relatively common in the aquarium trade and included here as L. cf. setigerum until a confirmed identity is established.

Mystacoleucus obtusirostris
Cyprinidae · Valenciennes, 1842
This species is occasionally marketed as 'Burmese Rainbow Barb' in the ornamental trade. others may have been exported in small numbers or as bycatch among shipments of other species. It was referred to as Mystacoleucus marginatus for decades, but that name is a simultaneous subjective synonym of M. obtusirostris following Kottelat (2013).

Nemacheilus saravacensis
Nemacheilidae · Boulenger, 1894
Images depict clear, tea-coloured forest streams with dense marginal vegetation and substrates of sand and/or small rocks and pebbles. It's also known from environments with sandy substrate and organic debris in the form of submerged roots/branches and le...

Nemacheilus selangoricus
Nemacheilidae · Duncker, 1904
N. selangoricus is most similar to N. spiniferus since it possesses acuminate scales above and below the lateral line on the caudal peduncle, a feature not shared with any other congener. It can however be distinguished by the following characters: presence of 8-12 very regular dark bars on flanks (vs. 10-13 irregularly-shaped bars in N. spiniferus), 3-5 times...

Nemacheilus spiniferus
Nemacheilidae · Kottelat, 1984
It's a member of the N. selangoricus group of species within the genus, an assemblage first recognised by Hadiaty and Kottelat (2009) and characterised by possession of two rows of horizontally-arran...

Oliotius oligolepisCheckered Barb
Cyprinidae · Bleeker, 1853
This species is also traded as 'checker barb', 'checkerboard barb', or 'island barb', and is among the most ubiquitous species available in the aquarium trade. It is farmed commercially in enormous numbers with wild examples rarely, if ever, available. It was formerly included in the polyphyletic catch-all genus Puntius which contained over 100 species, but this situation has been largely resolved since the turn of the century.

Oryzias celebensisCelebes Ricefish
Adrianichthyidae · Weber, 1894
Described from the Maros River (Salo Maros), southwestern Sulawesi, Indonesia and subsequently recorded from rivers and streams throughout the southwestern arm of the island including Lake Tempe (Danau Tempe), plus the Mota Talau River, East Timor state on the nearby island of Timor. More recently Herder and Chapuis (2010) reported it to be more widespread on Sulawesi, with new records pertaining to an unnamed small stre...

Oryzias eversi
Adrianichthyidae · Herder, Hadiaty & Nolte, 2012
The type locality is a karst pool around 30-40 m in length, 10m in width and up to 4 m deep. It contains still, transparent water, has a single inflow and outflow, is surrounded by rainforest and in September 2010 the water temperature was 21.5°C/70.7°F. The habitat is used by locals as a bathing pool and sympatric species included a nat...

Oryzias javanicusJavanese Ricefish
Adrianichthyidae · Bleeker, 1854
This species is widely-distributed throughout Peninsular Thailand, Malaysia (Malay Peninsula plus the states of Sabah and Sarawak, Borneo), Singapore and Indonesia, with records from the Riau Archipelago, Sumatra, Java, Borneo, Bali, Lombok, and Sulawesi existing in the latter. Type locality is 'Panimbang River, Perdana, Indonesia'. It's typically found in coastal, normally brac...

Oryzias sarasinorumSarasin's Buntingi
Adrianichthyidae · Popta, 1905
Utilises a strategy which has become known as 'pelvic brooding'. Spawning tends to occur in the early morning, with dominant males darkening in colouration and defending their space by driving away potential competitors, while approaching ripe females in a rigid 'head-down' position. The eggs normally number 8-12 and are expelled as a single mass while being fertilised simultaneously, after which they continue to hang from th...

Oryzias wolasiWolasi Ricefish
Adrianichthyidae · Parenti, Hadiaty, Lumbantobing & Herder, 2013
This species was discovered in 2009 and as far as we know it has only been collected for the aquarium hobby on a single occasion to date, by Jeffrey Christian of Maju Aquarium, Frank Evers and Hans-Georg Evers. Prior to description it was referred to as O. sp. 'Kendari', O. sp. 'neon' or O. sp. 'Sulawesi'.
Oryzias woworaeDaisy's Ricefish
Adrianichthyidae · Parenti & Hadiaty, 2010
The type locality is a karstic freshwater stream flowing under 80% forest cover with a mixed substrate of mud and sand plus patches of leaf litter. O. woworae was collected from a still pool around 3-4 m deep, opposite an affluent spring, where it was schooling with a species of Nomorhamphus which may turn out to be a form of N. ebrardtii but has subsequently appeared in the aquarium trad...

Pangio anguillaris
Cobitidae · Vaillant, 1902
One of a handful of Pangio spp. traded under the generic name 'eel loach'. Wild populations tend to differ in colour pattern to some extent, with some exhibiting a more intense lateral stripe while others display an irregular pattern of fine dark spots on the body, for example.

Pangio cuneovirgata
Cobitidae · Raut, 1957
Infrequently encountered in the aquarium trade, most often as bycatch among shipments of similar-looking congeners. It's included in the P. kuhlii group of closely-related species within the genus, and can be distinguished from other members by...

Pangio malayana
Cobitidae · Tweedie, 1956
Originally known only from Johor and Pahang states, Peninsular Malaysia but since recorded from the Batang Hari river drainage, Sumatra and the Kapuas system, Kalimantan Barat (West Kalimantan) province, Indonesian Borneo. Type locality is 'Tahan River, Pahang, Malaysia'.

Pangio oblongaBlack Kuhli Loach
Cobitidae · Valenciennes, 1846
Described from close to the city of Bogor, Jawa Barat (West Java) province on the island of Java, Indonesia, but currently considered widespread with recorded occurrences on Java, Sumatra, Borneo and mainland Peninsular Malaysia. Some populations exhibit lighter...

Pangio piperata
Cobitidae · Kottelat & Lim, 1993
Some Sumatran and Bornean populations of the highly variable P. shelfordii superficially resemble P. piperata which can cause issues with identification as the two often occur together. In general however the body patterning in P. piperata is than that of P. shelfordii and they differ in vertebral counts (mode 47 vs. 50, respectively).

Pangio semicincta'Kuhli' Loach
Cobitidae · Fraser-Brunner, 1940
This species is among the most frequently-misidentified in the hobby, almost always being traded as P. kuhlii. However the latter is currently considered endemic to Java, from where commercial collections are almost unheard of, and has possibly never been seen in aquaria.

Pangio shelfordii
Cobitidae · Popta, 1903
Patterning is highly variable depending both within and between populations and the species may comprise an assemblage containing a number of taxa (Kottelat and Lim, 1993; Tan and Kottelat, 2009). For example, those from Singapore and Johor possessing intricate mottling on the dorsal surface while individuals from Terengganu have a series of saddle-like markings either alternating or connecting with the midlateral markings.

Parosphromenus anjunganensis
Osphronemidae · Kottelat, 1991
It's care requirements, disposition, and especially conservation status dictate that it should be maintained alone or alongside a group of small, peaceful cyprinids such as Boraras or Sundadanio spp. Likewise, different Parosphromenus spp. should not be kept together since the females of many are very difficult to tell apart and some are undoubtedly capable of hybridising.

Parosphromenus bintan
Osphronemidae · Kottelat & Ng, 1998
This species is not generally available in the aquarium hobby on a commercial basis but is occasionally collected and distributed by private aquarists. It's name is sometimes misapplied to commercial shipments of other species, and there also exist a number of other fish with rounded caudal-fins that may or may not be conspecific, including P. sp. 'blue line' and P. sp. 'Selatan' from Sumatra.

Parosphromenus deissneriDeissner's Liquorice Gourami
Osphronemidae · Bleeker, 1859
P. deissneri was the only recognised member of the genus for almost a century following its description in 1859. As a result its name has and continues to be widely misapplied in both aquarium and ichthyological literature although it's probably always been very rare in the hobby, while a number of fishes previously identified under the name from other pa...

Parosphromenus linkei
Osphronemidae · Kottelat, 1991
This species is said to be slightly easier to maintain than the majority of congeners and is therefore a recommended choice for those new to maintaining Parosphromenus spp. in the aquarium. It's occasionally available on a commercial basis and we've seen it traded as 'moonspot licorice gourami' in the past. There exist at least three colour forms on...

Parosphromenus opallios
Osphronemidae · Kottelat & Ng, 2005
Endemic to Central Kalimantan (Kalimantan Tengah) province, Borneo, Indonesia although the full extent of its range remains somewhat unclear. Initial collections were from the southwestern tip of the province, in the Jelai Bila river basin near Sukamara and Lamand basin close to Pangkalan Bun, both of which are tributaries within the Arut drainage, while it's subsequently been recorded in the Benipah river system further east.

Parosphromenus ornaticauda
Osphronemidae · Kottelat, 1991
This species has occasionally appears in the aquarium trade in substantial quantities but is not an easy species to maintain in captivity and often susceptible to disease post-import. It's sometimes sold as 'ornate licorice gourami'. It's among the smallest members of the gen...

Parosphromenus quindecim
Osphronemidae · Kottelat & Ng, 2005
This species has occasionally been traded on a commercial basis and was known as P. sp. 'Manis Mata' prior to description, with the latter apparently referring to a location some 100 km away from the type locality where the fish do not occur. It's said to be slightly easier to maintain than the majority of congeners and is therefore a recommended choice for those ne...

Parosphromenus sp. 'Sentang'
Osphronemidae · authority not recorded
This fish has been widely available in the aquarium trade in recent years and is sometime referred to by the invented name P. 'sintangensis'. It displays a close resemblance to P. bintan and another unidentified fish known to aquarists as P. sp. 'blue line' although the inner bluish bands in the dorsal, anal and caudal fins are perhaps a little narrower in P. sp. 'Sentang' than the other two.

Pseudomugil cyanodorsalisNeon Blue-eye
Pseudomugilidae · Allen & Sarti, 1983
Euryhaline and thus capable of withstanding significant fluctuations in salinity and other water conditions. It's been recorded in full marine conditions as well as pure freshwater environments, and commonly inhabits coastal mangrove creeks and swamps. Such changes may occur on a daily or seasonal basis depending on locality, with some habitats influenced by daily tides whereas others become hypersal...

Pseudomugil gertrudaeSpotted Blue-eye
Pseudomugilidae · Weber, 1911
Described from 'Rivulet in sago forest at Ngaiguli, Terangan, Aru Island, Aru Islands, Maluku, Indonesia', corresponding to the island now normally referred to as 'Trangan' in the Aru Islands group, eastern Indonesia. The islands are located in the Arafura Sea, with western New Guinea to the north and the Arnhem Land Region of Australia's Northern Territory to the south, and though they lie within Maluku province of eastern Indonesia, are part of the Australian continent in a geological sense.

Pseudomugil sp. 'red neon'
Pseudomugilidae · authority not recorded
This fish first appeared in the aquarium hobby in 2011 and has been traded under various names including P. sp. cf. paskai, P. sp. 'red orange neon', P. sp. 'neon orange', P. sp. 'Irian' and P. 'iriani'. The majority of fish available tend to be male, presumably due to their brighter colour pattern. It was initially suspected to be a hybrid or sele...

Pseudomugil tenellusDelicate Blue-eye
Pseudomugilidae · Taylor, 1964
Euryhaline and mostly inhabits coastal floodplains where it's found in both fresh and brackish habitats, including tidal estuaries and salt marshes. It's particularly common in swamps, billabongs, and slow-moving streams where aquatic vegetation grows densely, but some populations have colonised upper sections of freshwater streams. Larger individuals may also move into main river channels. Tappin (2010) gives the following ranges of parameters based on those taken from various localities: temperature 27 - 38 °C, pH 5...

Puntigrus anchisporus
Cyprinidae · Vaillant, 1902
This species occasionally appears in the aquarium hobby, but the trade is largely reliant on commercially-produced 'tiger barbs' of questionable origin. It is distinguished from congeners by the following combination of characters: lateral line complete; 14 circumpeduncular scales; 21-23+2 scales in the lateral row; dorsal-fin black with red outer band; pelvic fins red.

Puntigrus pulcher
Cyprinidae · Rendahl, 1922
This species occasionally appears in the aquarium hobby, but the trade is largely reliant on commercially-produced 'tiger barbs' of questionable origin. It was considered a synonym of P. anchisporus for a number of decades following Alfred (1963), but revalidated by Kottelat and Tan (2011).

Puntigrus tetrazonaTiger Barb
Cyprinidae · Bleeker, 1855
P. tetrazona is traditionally considered to be among the most ubiquitous species available in the aquarium trade. Wild examples are rarely traded, however, and there exists ongoing confusion as to the identity of the commercially-produced 'aquarium' tiger barb. A number of selectively-bred, ornamental strains are available. The albino, 'green' (aka 'moss'), and 'golden' (leucistic) variants are particularly pop...

'Puntius' lineatusLined Barb
Cyprinidae · Duncker, 1904
One of four similar-looking, laterally-striped 'Puntius' spp. native to Southeastern Asia alongside 'P.' gemellus, 'P.' johorensis, and 'P.' trifasciatus. Of these 'P.' lineatus is most often confused with 'P.' johorensis by virtue of the fact that these two seem most common in the aquarium trade. Telling them apart is relatively simple since 'P.' lineatus has 0 - 1 pairs of barbels (vs. 2 pairs in the other three species), juv...

Rasbora dusonensis
Cyprinidae · Bleeker, 1850
The identity of this species was unclear for a number of decades prior to its redescription by Ng and Kottelat (2013). The confusion originated with Brittan (1954) who misidentified specimens of R. tornieri as R. dusonensis and was exacerbated by Alfred (1963) who concluded that the holotype of R. dusonensis was conspecific with R. myersi.

Rasbora tornieri
Cyprinidae · Ahl, 1922
Type locality is 'Central Sumatra, Indonesia', with additional records existing from Cambodia (Mekong drainage), Peninsular Malaysia (Perak River), Sumatra (from the Siak River, Riau province to the Musi River, South Sumatra (Sumatera Selatan) province) and Borneo (south and westwards from the Belait river basin in Brunei Darussalam to the Sambas drainage in West Kalimantan (Kalimantan Barat) province, Indonesia and probably in Sarawak, Malaysia).

Sicyopus exallisquamulus
Gobiidae · Watson & Kottelat, 2006
Live colouration of this species was not included in the original description but the specimens in our images were identified by Dr. Ronald E. Watson, the principal author, as S. exallisquamulus. It's normally misidentified and traded as the Sri Lankan endemic species Sicyopus jonklaasi. It is diagnosable from congeners by the following combination of characters: 14-15 pectoral-fin rays; both genders exhibit small, widely-spaced scales...

Sicyopus zosterophorus
Gobiidae · Bleeker, 1856
Type locality is given as 'Boleling, northern Bali, Indonesia' which appears to correspond to modern-day Buleleng, but this species is currently understood to have a patchy but wide distribution with a range stretching westwards from the Marquesas Islands (French Polynesia), throughout much of Vanuatu, New Caledonia, the Solomon Islands, Papua New Guinea, Palau, Fiji, Indonesia, the Philippines, Japan, Taiwan, and most recently, southern mainland China...

Sphaerichthys acrostomaGiant Chocolate Gourami
Osphronemidae · Vierke, 1979
This species is traded under several names of which others include 'sharp-nosed gourami', 'moonlight chocolate gourami', 'black-lined chocolate gourami' and 'black-tailed chocolate gourami', though it's far from common in the hobby. Its unique colour pattern makes it difficult to confuse with any of the three other members of the genus even in the absence of meristic data.

Sphaerichthys osphromenoidesChocolate Gourami
Osphronemidae · Canestrini, 1860
The genus Sphaerichthys currently comprises four species with S. osphromenoides by far the best known in the hobby. It's easily distinguishable from the congeners S. vaillanti and S. acrostoma since both exhibit a notably more elongate head and body profile, reverse sexual dimorphism (i.e. females are the more colourful/strongly-patterened), and are paternal mouthbrooders.

Sphaerichthys selatanensisCrossband Chocolate Gourami
Osphronemidae · Vierke, 1979
This species is only occasionally seen in the hobby and sometimes sold as 'cherry chocolate gourami'. It was originally described as a subspecies of S. osphromenoides since the two are very similar-looking but has been considered a species in its own right since the late 1980s. The two differ in the number ofrays (7 in S. selatanensis vs. 9-10 in S. osphromenoides),rays (7 vs. 8),...

Sphaerichthys vaillantiVaillant's Chocolate Gourami
Osphronemidae · Pellegrin, 1930
This species is traded under several names of which others include 'Samurai gourami' and 'Samurai Zebra Chocolate Gourami'. Though the former of these is arguably the most common, these names are potentially misleading since the fish is neither especially combative nor from Japan. Its unique colour pattern makes it difficult to confuse with any of the three other members of the genus even in the abse...

Stiphodon atratus
Gobiidae · Watson, 1996
Type locality is given as 'Stream at end of long narrow bay, Waigeo Island, Irian Jaya, Indonesia', with the species also known from rivers draining the northern slope of New Guinea as well as Halmahera Island (Indonesia), the Admiralty Islands (Papua New Guinea), the Bismarck Archipelago (Papua New Guinea), D'Entrecasteaux Islands (Papua New Guinea), Louisiade Archipelago (Papua New Guinea), Bougainville (Papua New Guinea), Vanuatu, and...

Stiphodon maculidorsalisOrange-fin Stiphodon
Gobiidae · Maeda & Tan, 2013
This species was referred to as S. sp. 'orange fin' or S. sp. 'ST01' prior to being offically named and is one of the more commonly-traded members of the genus, though often in batches containing only one gender, a mixture of species, or misidentified under an incorrect name such as S. zebrinus. It can be told apart from congeners by the following combination of characters: usually 9 soft second dorsal-fin rays; 15 soft pectoral-fin rays; first dorsal-fin in male poin...

Stiphodon ornatusRainbow Stiphodon
Gobiidae · Meinken, 1974
This species is traded as S. sp. 'rainbow', S. sp. 'gold fin', or S. sp. 'gold cheek' and is among the more widely-available members of the genus although its identity was unclear prior to 2013. The most commonly-traded fish certainly appears to...

Stiphodon semoniCobalt Blue Goby
Gobiidae · Weber, 1895
This species has been traded for a number of years, though not always under the correct name. We've seen it on sale as S. elegans or S. atropurpureus on numerous occasions, for example, and other trade names include 'Sumatran blue neon goby', 'cobalt blue goby' and 'freshwater neon goby'. Further confusion has arisen because other species are sometimes sold as S. semoni meaning identification has not always been easy and there ...

Systomus orphoides
Cyprinidae · Valenciennes, 1842
The genus Puntius is currently viewed as something of a catch-all for well over 100 species of small to mid-sized cyprinid. Most experts agree that a full revision is required with the likely outcome that many species will be placed into new or different genera since it is clearly polyphyletic. When describing the grouping in 1822 Hamilton identified the defining characteristics as: presence or absence o...

Trigonopoma gracile
Cyprinidae · Kottelat, 1991
This species occurs in several colour forms depending on collection locality with some exhibiting more intense pigmentation in the fins or an additional reddish lateral stripe, for example. It's sometimes said to closely resemble and occur sympatrically with Rasbora agilis, but that name is currently considered a junior synonym of the congener Trigonopoma pauciperforatum. R. agilis had previously been us...

Trigonopoma pauciperforatumGlowlight Rasbora
Cyprinidae · Weber & de Beaufort, 1916
This species is also sold as the 'redline' rasbora which is something of a misnomer as in reality the colour of the lateral stripe that gives rise to the name can vary from deep orange to golden depending upon the collection locality of the fish as well as diet, condition, and even mood. Some specimens also have a second, darkish stripe beneath the other which seems to vary in length and intensity depending on a similar array of factors. Older fish tend to possess a greater degree of black edging to the scales, especially in the ventral portion of the body.

Trigonostigma hengeli
Cyprinidae · Meinken, 1956
T. hengeli is sometimes seen for sale with the trade name of 'glowlight rasbora' due to the distinctive orange patterning on the posterior part of the body but we've refrained from using that name here because it's also commonly applied to Trigonopoma pauciperforatum. It can be confused with the similar-looking T. heteromorpha and T. espei although on close inspection they're actually quite easy to tell...

Trigonostigma heteromorphaHarlequin
Cyprinidae · Duncker, 1904
T. heteromorpha was first exported for aquaria in the early 1900s and has gone on to become one of the most familiar, enduring species in the hobby. It has suffered as a result of its popularity to a certain extent with the mass-produced fish we see today lacking much of the colour seen in wild specimens and even exhibiting morphological deformities in some cases. Several selectively-bred ornamental strains have also...

Vaillantella maassiFork-tailed Loach
Vaillantellidae · Weber & de Beaufort, 1912
This species is traded under various names including 'chocolate scissor-tailed loach', chocolate long-finned loach', 'red line cobra loach', 'spiny eel loach' and 'dragon loach'. It's apparently difficult to find in its natural habitats and thus time-consuming to collect, meaning it's rarely traded in numbers, sought after by enthusiasts and tends to carry a relatively high price tag when available. The genus currently contains just three...

Xenentodon canciloides
Belonidae · Bleeker, 1854
This species is a near-exclusive inhabitant of the upper water column and appreciates surface cover in the form of floating or overhanging vegetation. Other décor is relatively unimportant but can consist of a sandy substrate with leaf litter plus some large driftwood branches and twisted roots. Plants which can grow rooted in sand can al...
Xiphophorus helleriiGreen Swordtail
Poeciliidae · Heckel, 1848
Wild swordtails are a fairly basic green colur. However the vast majority of swordtails available in the hobby today are hybrids of X.helleri with X.maculatus or X.variatus. There are a huge number of selectively-bred varieties available, including wagtail, lyretail, tuxedo, albino, neon, red, green and hi-fin. Swordtails may undergo what appears to be a change in sex. In young fish this may simply be late development. However some adult females develop male characteristics which is thought ...

Allenbatrachus grunniensFreshwater Toadfish
Batrachoididae · Linnaeus, 1758
This species is relatively common in the aquarium hobby but contrary to popular belief is not venomous in any way. Its dorsal and opercular spines can pierce the skin, however, meaning extreme caution is necessary when netting it or performing aquarium maintenance. The genus Allenbatrachus was erected in 1997 to accom...

Anabas testudineusClimbing Perch
Anabantidae · Bloch, 1792
This species isn't especially popular in the aquarium trade but is undoubtedly interesting despite its lack of colour. In addition to its survival ability in the absence of water it's also capable of producing audible sounds though the purpose of these has not been fully-studied. Naturally-occurring xanthic and albino forms have also been recorded. There is considerable confusion as to the taxonomic status of the two species currently occupying this genus, with ichthyologists widely...

Bagarius yarrelliGoonch
Sisoridae · Sykes, 1839
This species is clearly unsuitable for the home aquarium given its eventual size and natural behaviour, and we know of only a handful of private aquarists with the facilities required to house it long-term. The grouping currently contains four species but is in urgent need of review with a number of additional taxa thought to exist and B. yarrelli possibly representing a synonym of B. bagarius.

Betta chloropharynxGreen Throat Mouthbrooder
Osphronemidae · Kottelat & Ng, 1994
B. chloropharynx is included in the Betta waseri group/complex of closely-related species within the genus, an assemblage which also includes a handful of potentially new species such as B. sp. 'Medas' on an unofficial basis. The easiest way to distinguish these is by examining the throat markings which vary according to species. In this case the lighter of these form a shape that roughly resembles a horizontal figure of ei...

Betta pallifina
Osphronemidae · Tan & Ng, 2005
This species is included in the Betta unimaculata complex of closely-related species within the genus, of which members share the following set of characters: body long and slender with depth at dorsal fin origin 18-25 % SL; head large and blunt with width 19-24 % SL; long maxilla and lower lip with distance from tip of lower jaw to posterior end of maxilla 27-54 % HL; caudal-fin rounded in shape, occasionally with elongated median rays; pelvic-fin short and filamentous; dorsal and anal fins relatively pointed.

Channa marulioidesEmperor Snakehead
Channidae · Bleeker, 1851
This species is often confused with the nominal congeners C. marulius (Hamilton, 1822) and C. melanoptera (Bleeker, 1855) with all three presenting taxonomic problems. For example, C. marulioides exhibits a number of variations in colour pattern depending on collection locality with the most common possessing a brownish base colour with a series of dark, chevron-like markings along each flank and some scales margined posteriorly in white.

Channa micropeltesGiant Snakehead
Channidae · Cuvier, 1831
C. micropeltes is also referred to as 'Indonesian', 'red', or 'redline' snakehead, the latter names in reference to the appearance of juveniles which often appear in the ornamental trade despite its unsuitability for home aquaria. It is somewhat hyperbolised in the media as a fearsome, invasive "monster" fish with a reputation for killing more fish than it can eat, and even the occasional human, although in reality...

Chitala lopisGiant Featherback
Notopteridae · Bleeker, 1851
This species is not collected for the aquarium trade at time of writing. In contrast to other members of the genus older juvenile and adult individuals lack dark markings on the body while the jaw is more pronounced.

Crossocheilus cobitis
Cyprinidae · Bleeker, 1854
Given its wide natural range it seems logical that this species is or has been available in the aquarium trade, although its correct name may never have been applied. It is told apart from congeners by the following combination of characters: two pairs of barbels; a continuous midlateral stripe from the tip of the snout to the base of the caudal-fin, with a conspicuous small blotch at the posterior extremity, faintly marked on the caudal-fin; a faint mark between the anus and the anal-fin origin in juveniles; a narrow mouth.

Ctenopharyngodon idellaGrass Carp
Cyprinidae · Valenciennes, 1844
Despite being a wholly unsuitable aquarium subject, C. idella is often traded as such, with an albino form having been developed specifically for the ornamental market. Individuals which have outgrown their aquarium or pond should never be released into natural waters, either, since this species has proven capable of causing serious environmental damage under a wide range of climatic conditions.

Cyclocheilos enoplos
Cyprinidae · Bleeker, 1849
In the Mekong, it has been observed to migrate upstream from Phnom Penh to Khone Falls between November and February, returning downstream between May and August. The downstream migration ends in the Mekong delta area in Vietnam, where the fish remain until the floods reach their peak in October and November. These lower Mekong migrations mostly comprise juveniles and sub-adults, whereas above Khone Falls...

Datnioides microlepisIndonesian Tiger Perch
Datnioididae · Bleeker, 1854
In aquarium literature this species is also referred to as 'fine scaled tiger fish', 'Indonesian tiger fish', 'Sumatran tiger fish', 'Indo datnoid', and 'Indo dat'. The common name of 'tiger fish' is also used in reference to the African alestid genus Hydrocynus, and the more appropriate 'tiger perch' was suggested by Roberts and Kottelat (1994).

Hampala macrolepidotaHampala Barb
Cyprinidae · Kuhl & van Hasselt, 1823
This species is also known by the vernacular 'jungle perch' or 'sidebar barb' and should not be considered an aquarium subject in all but the most extreme circumstances since it can grow to over 2 feet in length, weigh in excess of 5 kg and is a powerful, pelagic predator. It's also a popular sport fish with a reputation for striking hard.

Hemibagrus wyckiiCrystal-eyed Catfish
Bagridae · Bleeker, 1858
Aggressively territorial and incompatible with other fishes in all but the largest public installations and even then may attack its tankmates. It's also one of few freshwater fishes that appear unafraid of humans meaning care must be exercised when performing maintenance.

Labeo chrysophekadionBlack Shark
Cyprinidae · Bleeker, 1849
L. chrysophekadion is also known as 'black sharkminnow'. It continues to be available in the ornamental trade despite its patent unsuitability for the home aquarium, and an albino form has been selectively bred for the purpose. It can be distinguished from other members of the genus by the following combination...

Leptobarbus hoeveniiMad Barb
Cyprinidae · Bleeker, 1851
Apparently native to Peninsular Malaysia plus the Greater Sunda Islands of Borneo, Sumatra, and Java. Reports of this species from the Mekong, Chao Phraya, and other rivers in Indochina refer to the congener L. rubripinna (see 'Notes'). Type locality is 'Indonesia: Borneo: Kalimantan Selatan: Banjarmasin'.

Macrochirichthys macrochirusGiant Sword Minnow
Cyprinidae · Valenciennes, 1844
It is thought to have been extirpated from the Chao Phraya and Mae Klong rivers, Lake Songkhla, and the entire island of Java due to a variety of anthropogenic factors, and the Mekong populations have also been drastically reduced. In particular, it is sensitive to pollution and gillnetting, and is heavily overfished.

Notopterus notopterusBronze Featherback
Notopteridae · Pallas, 1769
This species is also referred to as 'Asian knifefish' or 'ghost knifefish' in the aquarium trade in the aquarium trade but arguably has no place in the ornamental hobby given its adult size and specialised requirements. It is sometimes confused with the African species Xenomystus nigri but is easily told apart by its larger adult size and presence (vs. absence) of a dorsal fin.

Phalacronotus apogon
Siluridae · Bleeker, 1851
P. apogon has formerly been placed within the genera Kryptopterus, Micronema (Rainboth, 1996) and more recently Phalacronotus (Ferraris, 2007) and is an important food fish across much of its native range. It's very similar to P. micronema but can be told apart by its longer head (HL fits 4.6± 5.3 times in...

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...

Sundasalanx microps
Sundasalangidae · Roberts, 1981
The genus Sundasalanx is distributed throughout much of Southeast Asia and currently comprises seven species which have primarily been distinguished on the basis of oral and dental morphology, gill rakers and eye size. S. microps possesses 0-3 small conical teeth on ceratobranchial 5, 0-2 minute gill rakers on the first arch and a small eye measuring less...

Oryzias asinuaAsinua Ricefish
Adrianichthyidae · Parenti, Hadiaty, Lumbantobing & Herder, 2013
When the type series was collected the Sungai Asinua contained clear, slow to fast-moving water with a temperature of 26 °C. The substrate was composed of mud, sand an...

Brachygobius xanthozonus
Gobiidae · Bleeker, 1849
B. xanthozonus can be considered something of an enigma since its name has been widely misapplied in aquarium literature for decades, when in reality it's probably never been exported for the ornamental trade. The majority of fish seen labelled as such are either B. doriae or B. sabanus, themselves often misidentified.

Garra borneensis
Cyprinidae · Vaillant, 1902
Substrates are generally composed of gravel, rocks, boulders or bedrock carpeted with a rich biofilm formed by algae and other micro-organisms. At a habitat in the Mendawai river basin in central Kalimantan, H. borneensis was collected from a foothill stream running swiftly over a rock and gravel substrate with clear water of pH 6.4.

Hampala bimaculata
Cyprinidae · Popta, 1905
Predominantly a riverine fish preferring clear, well-oxygenated, running waters with substrates of sand, gravel, rock or mud, typically flowing through tropical forest. In the habitat seen in our images sympatric fish species included Barbonymus balleroides, B. collingwoodi, Cyclocheilichthys repasson, C. apogon, Diplocheilichthys pleurotaenia, Garra borneensis, Leptobarbus hosii, and an unidentified Gastromyzon sp.

Hemibagrus planiceps
Bagridae · Valenciennes, 1840
This species is now considered endemic to Java but has been confused with the congeners H. gracilis (from eastern Peninsular Malaysia), H. velox (Sumatra) and H. bongan (Borneo) in the past, while the population formerly considered to inhabit northwestern Peninsular Malaysia has been described as H. divaricatus (Ng and Kottelat, 2013).

Labiobarbus fasciatus
Cyprinidae · Bleeker, 1853
Known from the Pahang River system in southern Peninsular Malaysia, and the Greater Sunda Islands of Sumatra and Borneo. On the latter records exist from the Kapuas, Barito, and Mahakam watersheds in Kalimantan, the Indonesian portion of the island Type locality is 'Pangabuang, Lampong Province, Sumatra, Indonesia'.

Luciosoma pellegrinii
Cyprinidae · Popta, 1905
The five species which currently comprise Luciosoma can be distinguished by elements of colour pattern. Popta described the colour pattern of L. pellegrinii as follows: body colour olive dorsally, with dark-edged scales, yellow ventrally; a lateral series of dark spots on the flank forming a midlateral band which extends onto the opercle but not the head; 4-8 blackish-brown, distinctly-separate spots on the lateral line; fins yellow; dorsal and anal fins with a blackish-brown band; anterior half of some pectoral-fin rays blackish-brown...

Luciosoma spilopleura
Cyprinidae · Bleeker, 1855
This species is poorly known in general and is not present in the ornamental trade, although its name is widely misapplied to other Luciosoma species. Its congeners are mostly marketed as 'apollo shark', 'shark minnow', or similar, and often labelled with incorrect scientific names. Identification of the fish pictured here is based on Bleeker (1855, 1860) and Roberts (1989), plus drawings by Bleeker, thus...

Nematabramis borneensis
Cyprinidae · Inger & Chin, 1962
It looks particularly similar to N. alestes with both species possessing a colour pattern comprising a dark lateral stripe on the body, but can be distinguished immediately by possessing barbels longer than the head (vs. shorter than the head in N. alestes).

Nematabramis everetti
Cyprinidae · Boulenger, 1894
Nematabramis species are found a variety of habitat-types, from swiftly-flowing affluent streams to pools, lakes, and degraded swamps. Based on the available collection records juveniles and subadults of N. everetti display a preference for fast-moving water whereas adults are found in deeper, slower stretches of minor tributaries.

Nematabramis steindachnerii
Cyprinidae · Popta, 1905
Endemic to northern and central Borneo, with records from the Malaysian states of Sarawak and Sabah, Brunei Darussalam, and the Indonesian provinces North Kalimantan (Kalimantan Utara) and East Kalimantan (Kalimantan Timur). Type locality is 'Kajan River, eastern slope of central Kalimantan, Indonesia [Borneo]'.

Puntigrus navjotsodhii
Cyprinidae · Tan, 2012
The type series was collected from a small clear-water stream with a pH of 6.0, forming a series of riffles and deeper pools, with a maximum width of 5 metres and depth ranging from 10 cm to 1 metre. The substrate was composed of sand gravel and rocks, with some leaf litter and overhanging marginal vegetation.