RSS Facebook Twitter YouTube




Gastromyzon lepidogaster ROBERTS, 1982


Gastromyzon: from the Greek gaster, meaning ‘stomach’ and myzo, meaning ‘to suckle’.

lepidogaster: from the Greek lepis, meaning ‘scale’, and gaster, meaning ‘stomach’, in reference to the extensive squamation on the abdomen.


Order: Cypriniformes Family: Gastromyzontidae


Type locality is ‘Mengalong River, Beaufort District, Sabah, northern Borneo’, but G. lepidogaster is the most widely-distributed member of the genus and in Sabah state  (Malaysia) it’s also known to occur in the rivers Padas, Kimanis, Petagas, Labuk, Kinabatangan, Segama, Kalabakan, plus all rivers draining into Wallace Bay.

Additional records exist from the Temburong River in Brunei Darussalam and the Sebuku, Sembakung and Sesayap drainages in East Kalimantan province, Indonesia.

All members of the genus are endemic to Borneo with over half restricted to just a single river basin or sub-basin.


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.

Aquatic plants are uncommon and while riparian vegetation may be present these loaches tend to be most abundant in partially or fully-shaded zones.

Field observations have revealed that individuals typically position themselves facing into the flow, either along the sides, behind or under rocks, their specialised morphology (see ‘Notes’) allowing them to forage and maintain a particular spot without being swept away.

In the Danum Valley, Sabah, G. lepidogaster was collected from headwater streams of the Kuamut and Segama rivers in shallow (maximum depth 60 cm), fast-flowing, unshaded riffle habitats. PH was measured to range between 7.2-8.7.

In the Kuamut River sympatric species included the congeners G. aequabilis, G. ornaticauda, and G. pariclavis plus Homalopteroides stephensoni, Nemacheilus elegantissimus, N. olivaceus, Neogastromyzon crassiobex, Protomyzon griswoldi and P. whiteheadi.

The same species were present in the Segama with the exception that congeners encountered were G. danumensis and G. spectabilis.

In the Batu Apoi Forest Reserve, Brunei, G. lepidogaster was found in small tributary streams of the Belalong River, comprising partially-shaded hill streams of 1-5 metres in width broken up by cascades ranging from 2-3 metres to 15 metres in height.

Substrates varied from loose shale to large rocks and boulders, and the water was of pH 6.0 and flowing quickly.

Here G. lepidogaster was located on a particular kind of dark rock, usually in a pair comprising both green and barred forms (see ‘Notes’).

Other fishes present included Barbonymus collingwoodi, Hampala bimaculata, Nematabramis steindachneri, Osteochilus cf. ingeriRasbora argyrotaenia, Tor tambra, Pangio cf. mariarum, Gastromyzon cranbrooki, G. punctulatus, Glaniopsis sp., Neogastromyzon brunei, Parhomaloptera microstoma, Protomyzon sp., Hemibagrus sp., Ompok platycephalus, Pterocryptis furnessi, Macrognathus maculatus and Mastacembelus unicolor.

Maximum Standard Length

90 – 100 mm. The largest specimen known measured 100.4 mm.

Aquarium SizeTop ↑

An aquarium with base dimensions of 120 ∗ 30 cm or equivalent is large enough to house a group.


Most importantly the water must be clean and well-oxygenated so we suggest the use of an over-sized filter as a minimum requirement.

Turnover should ideally be 10-15 times per hour so additional powerheads, airstones, etc. should also be employed as necessary.

Base substrate can either be of gravelsand or a mixture of both to which should be added a layer of water-worn rocks and pebbles of varying sizes.

Aged driftwood can also be used but avoid new pieces since these usually leach tannins that discolour the water and reduce the effectiveness of artificial lighting, an unwanted side-effect since the latter should be strong to promote the growth of algae and associated microorganisms.

Exposed filter sponges  will also be grazed, and some enthusiasts maintain an open filter in the tank specifically to provide an additional food source.

Although rarely a feature of the natural habitat aquatic plants can be used with adaptable genera such as MicrosorumCrinum and Anubias spp. likely to fare best. The latter are particularly useful as their leaves tend to attract algal growth and provide additional cover.

Since it needs stable water conditions and feeds on biofilm this species should never be added to a biologically immature set-up, and a tightly-fitting cover is necessary since it can literally climb glass.

While regular partial water changes are essential aufwuchs can be allowed to grow on all surfaces except perhaps the viewing pane.

Water Conditions

Temperature: For general care 18 – 24 °C is recommended but it can withstand warmer conditions provided dissolved oxygen levels are maintained.

pH6.0 – 8.5

Hardness36 – 215 ppm


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 using a mixture of natural ingredients bound with gelatin are very useful since they can be tailored to contain a high proportion of fresh vegetables, Spirulina and similar ingredients.

For long-term success it’s best to provide a mature aquarium with a plentiful supply of algae-covered rocks and other surfaces.

If unable to grow sufficient algae in the main tank or you have a community containing numerous herbivorous fishes which consume what’s available quickly it may be necessary to maintain a separate tank in which to grow algae on rocks and switch them with those in the main tank on a cyclical basis.

Such a ‘nursery‘ doesn’t have to be very large, requires only strong lighting and in sunny climates can be kept outdoors. Algal type is also important with diatoms and softer, green varieties preferred to tougher types such as rhodophytic ‘black brush’ algae.

Gastromyzontids are often seen on sale in an emaciated state which can be difficult to correct. A good dealer will have done something about this prior to sale but if you decide to take a chance with severely weakened specimens they’ll initially require a constant source of suitable foods in the absence of competitors if they’re to recover.

Behaviour and CompatibilityTop ↑

Very peaceful although its environmental requirements limit the selection of suitable tankmates somewhat, plus it should not be housed with any much larger, more aggressive, territorial or otherwise competitive fishes.

Potential options include small, pelagic cyprinids such as TanichthysDanio, and Rasbora, stream-dwelling gobies from the genera RhinogobiusSicyopterus, and Stiphodon, plus rheophilic catfishes like GlyptothoraxAkysis and Hara spp.

Some loaches from the families Nemacheilidae, Balitoridae and Gastromyzontidae are also suitable but others are not so be sure to research your choices thoroughly before purchase.

Gastromyzon spp. tend to exist in loose aggregations in nature so buy a group of 4 or more if you want to see their most interesting behaviour.

They’re territorial to an extent with some individuals appearing more protective of their space than others, often a prime feeding spot.

Sexual Dimorphism

Adult females are noticeably heavier-bodied and often a little larger than males; these differences are more apparent when viewing the fish from above or below.


Has not been bred in aquaria and the only observations we know of for any member of the genus were made by German aquarist Philipp Dickmann and published in a hobbyist magazine during 2001.

He collected wild specimens of G. scitulus (identified as G. punctulatus at the time) and G. monticola, and attempted to spawn both using different methods.

Initially a pair of G. scitulus were placed in a 30 litre tank without substrate or filtration but heavily-aerated and containing some broken flower pots, boulders and floating plants for cover.

These were offered a rich diet with plenty of live and frozen mosquito larvae to bring them into breeding condition.

The temperature was then raised to 82.4°F/28°C over a period of 8 weeks and feeding increased; these conditions were maintained for 3 weeks during which the temperature unintentionally rose to 89.6°F/32°C.

After courtship behaviour was observed cool water changes were conducted to bring water temperature down to 77°F/25°C and the fish spawned during a period of low air pressure; at the point of climax their bodies are depicted to interlock away from the substrate.

At least 100 tiny (diameter <1 mm), sinking, non-adhesive eggs were observed and at this point the adults were removed.

The eggs began to hatch in around 3 days and the fry were initially photophobic and required an infusoriatype diet due to their small size (~3 mm SL). Apparently the plants in the tank began to rot resulting in a loss of water quality and after 3 weeks all the fry were dead.

More success was had with G. monticola, this time using a 160 litre tank with a coarse gravel substrate, some pieces of slate propped up against the rear pane, a clump of a Cryptocoryne sp. and a piece of driftwood.

Water temperature was maintained at 75.2°F/24°C and GH was 10-12°. This was again unfiltered but heavily-aerated with Ambastaia sidthimunkiPangio sp. and a large population of the burrowing snail Melanoides tuberculata also in residence.

On this occasion small numbers of fry simply began to appear over time, and spawning was observed continuously over a period of 12 months.

NotesTop ↑

G. lepidogaster is occasionally available in the aquarium trade, with the orange form (see below) particularly sought after.

It can be distinguished from congeners by the following combination of characters: large specimens with a plain brown, grey or black body when preserved, green or orange in life with dorsum of head plain brown; sub-adults and juveniles with black or dark brown body, 8-9 yellowish to cream bars, flanks with complete or interrupted bars forming a series of blotches, head dark brown with cream reticulated pattern; secondary rostrum absent; postoral pouch absent; subopercular groove absent; gill slit lunate; sublacrymal groove present; snout rounded when viewed from above; abdomen completely covered with fine scales as far as pectoral-fin origin; 55-69 lateral line scales; pelvic-fin not overlapping anal-fin origin.

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  spp. are placed into various species groups (putative assemblages of species which may or may not be monophyletic) for ease of reference, and G. lepidogaster is included in the G. lepidogaster group which also includes G. psiloetron.

Members are defined by a combination of characters including: abdominal scales present; large adult size; gill slit lunate; subopercular groove absent; juveniles and subadults with cream bars on a brown dorsum, interrupted on flanks to form diamond-shaped markings; adults with dark brown or black body when preserved, brown, lime green or orange when live; secondary rostrum absent; postoral pouch absent; lower lip with densely-arranged, small and branching papillae.

The current arrangement of species groups is as follows:

G. borneensis group: G. borneensisG. monticolaG. ornaticaudaG. cranbrookiG. cornusaccusG. extrorsusG. introrsusG. bario.
G. punctulatus group: G. aeroidesG. punctulatusG. katibasensis.
G. fasciatus group: G. fasciatusG. praestans.
G. contractus group: G. contractusG. megalepisG. umbrus.
G. ctenocephalus group: G. ctenocephalusG. scitulus.
G. lepidogaster group: G. lepidogasterG. psiloetron.
G. ridens group: G. ridensG. crenastusG. stellatusG. zebrinus.
G. danumensis group: G. danumensisG. aequabilisG. ingeri.
G. pariclavis group: G. pariclavisG. embalohensisG. venustusG. spectabilisG. russulusG. viriosus.
G. ocellatus group: G. ocellatusG. farragus.
G. auronigrus group: G. auronigrus.

Gastromyzon spp. have specialised morphology adapted to life in fast-flowing water. The paired fins are orientated horizontally, head and body flattened, and pelvic fins fused together.

These features form a powerful sucking cup which allows the fish to cling tightly to solid surfaces. The ability to swim in open water is greatly reduced and they instead ‘crawl’ their way over and under rocks.

The family Gastromyzontidae is currently considered valid as per Kottelat (2012).

It contains a number of genera which had formerly been included in several families and subfamilies, most recently Balitoridae, of which the most well-known in the aquarium hobby include Beaufortia, Formosania, Gastromyzon, Pseudogastromyzon, Hypergastromyzon, Liniparhomaloptera, Sewellia, and Vanmanenia.


  1. Roberts, T. R., 1982 - Proceedings of the California Academy of Sciences (Series 4) v. 42 (no. 20): 497-524
    The Bornean gastromyzontine fish genera Gastromyzon and Glaniopsis (Cypriniformes, Homalopteridae), with descriptions of new species.
  2. Inger, R. F. and P. K. Chin, 1961 - Copeia 1961(2): 166-176
    The Bornean cyprinoid fishes of the genus Gastromyzon Günther.
  3. Kottelat, M., 2012 - Raffles Bulletin of Zoology Supplement 26: 1-199
    Conspectus cobitidum: an inventory of the loaches of the world (Teleostei: Cypriniformes: Cobitoidei).
  4. Kottelat, M., 2013 - Raffles Bulletin of Zoology Supplement 27: 1-663
    The fishes of the inland waters of southeast Asia: a catalogue and core bibliography of the fishes known to occur in freshwaters, mangroves and estuaries.
  5. Martin-Smith, K. M. and H. H. Tan, 1998 - Raffles Bulletin of Zoology 46(2): 573-604
    Diversity of freshwater fishes from eastern Sabah: annotated checklist for Danum Valley and a consideration of inter- and intra-catchment variability.
  6. Rachmatika, I., 1998 - Raffles Bulletin of Zoology 46(2): 651-659
    Gastromyzon embalohensis, a new species of sucker loach (Teleostei: Balitoridae) from the Bentuang Karimun National Park, West Kalimantan, Indonesia.
  7. Tan, H. H., 2006 - Natural History Publications (Borneo), Kota Kinabalu: 1-245
    The Borneo suckers. Revision of the Torrent Loaches of Borneo (Balitoridae: Gastromyzon, Neogastromyzon).
  8. Tan, H. H. and K. M. Martin-Smith, 1998 - Raffles Bulletin of Zoology 46(2): 361-371
    Two new species of Gastromyzon (Teleostei: Balitoridae) from the Kuamut headwaters, Kinabatangan basin, Sabah, Malaysia.

No Responses to “Gastromyzon lepidogaster”

Leave a Reply

You must be logged in to post a comment.