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Trichopsis vittata

Croaking gourami

Cuvier, in Cuvier & Valenciennes, 1831

Formerly Osphromenus vittatus Cuvier, in Cuvier & Valenciennes, 1831 · Trichopus striatus Bleeker, 1850 · Trichopsis harrisi Fowler, 1934

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Specimen from Kota Tinggi, Johor state, Peninsular Malaysia.
Specimen from Kota Tinggi, Johor state, Peninsular Malaysia.Zhou Hang

Quick facts

Length
70mm SL2.8in SL
Tank base
60 × 30cm24 × 12in
Temp
22–28°C72–82°F
pH
5.0–7.5
Hardness
1–15dGH

Difficulty6 of 6 measures

Beginner

More bars, more demanding.

Space
modest tank
Water
tap water
Temp
unfussy
Temperament
peaceful
Social
in a pair
Compatibility
community tank

The common name is derived from the ability of genus members to produce audible sounds via a specialised pectoral mechanism which is unique within the family Osphronemidae. The structure comprises modified pectoral-fin tendons and muscles which are stretched and plucked by basal elevations of two fin rays in a similar way to guitar strings via rapid beating of the fins. The pectoral-fins beat alternately, each able to generate short or long bursts of sound. These sounds are produced by both sexes, predom...

Etymology

Trichopsis: from the Ancient Greek θρίξ (thríx), meaning 'hair', and ὄψις (ópsis), meaning 'aspect, appearance', presumably in reference to the filamentous fin extensions most evident in males.

vittata: from the Latin vittatus, meaning 'banded'.

Distribution

Currently accepted to occur throughout much of Indochina, including the lower Mekong River basin in Laos, Cambodia, Viet Nam, throughout southern Thailand, the lower Salween basin in Myanmar, Peninsular Malaysia, and Singapore. Records from the Greater Sunda Islands of Borneo, Sumatra, and Java might refer to a distinct species and require investigation.

Feral populations are established in several countries, including the Philippines, India, and U.S.A.

Type locality is 'Java, Indonesia'.

Habitat

Found in all types of still to slow-moving, predominantly lowland habitat, including swamp forest, peat swamps, floodplains, river tributaries, irrigation canals, paddy fields, and roadside ditches. Displays a distinct preference for sluggish to still environments with dense growths of aquatic or riparian vegetation.

Aquarium size

Standard length
70mm SL2.8in SL
Aquarium base
60 × 30cm24 × 12in
Volume
~54litres~14US gal

An aquarium with dimensions of 60 ∗ 30 ∗ 30 cm24 ∗ 12 ∗ 12 in is suitable for a single pair. A group would require more space.

Maintenance

This species fares best in a well-planted, shady aquarium with plenty of surface cover in the form of tall stem plants, floating varieties, or tropical lilies. Cryptocoryne spp. are also a good choice.

Driftwood can also be used and other plants such as Microsorum or Taxiphyllum spp. may be attached to it. Small clay plant pots, lengths of plastic piping or empty camera film cases can also be included to provide further shelter.

The addition of dried leaf litter offers additional cover and brings with it the growth of microbe colonies as decomposition occurs. These can provide a valuable secondary food source for fry, while tannins and other chemicals released by the decaying leaves are considered beneficial.

As it naturally inhabits sluggish environments strong water movement should be avoided, with an air-powered sponge filter set to turn over gently adequate. Keep the aquarium well-covered and do not fill it to the top since it requires occasional access to the layer of humid air that will form above the water surface, and is an excellent jumper.

Water conditions

Temperature
22–28°C72–82°F
pH
5.0–7.5
Hardness
1–15dGH

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Diet

Stomach analyses of wild fish have demonstrated them to prey on an assortment of aquatic and terrestrial invertebrates.

Captive fish will normally accept dried products once they are recognised as edible, but should be offered plenty of small live or frozen foods such as Daphnia, Artemia or chironomid larvae (bloodworm) to ensure development of optimal colour and condition.

Behaviour and compatibility

This species is peaceful unless breeding. It can be maintained in a pair or group, and will display some interesting behavioural interactions under the latter circumstances.

Sexual dimorphism

Males are larger than females and possess extended rays in the pelvic, dorsal, anal, and caudal fins. Sexually mature individuals can also be sexed by placing a strong light behind the fish, with the ovaries in females clearly visible below the swim bladder.

Reproduction

Bubble nester. Soft water with a slightly raised temperature is said to induce reproductive behaviour.

The aquarium should have the tightest-fitting cover possible (some breeders use clingfilm/plastic wrap) because the fry need access to a layer of warm, humid air, without which development of the labyrinth organ can be impaired.

The pair need not be separated prior to spawning. The male tends to construct his nest within a raft of surface vegetation, under an overhang or in a cavity.

Once the nest is complete, the male displays to potential mates using his elongated dorsal, anal, and caudal fins, and if receptive the female approaches in a vertical, head-up position, emitting a series of 'purring' sounds (see 'Notes'). Spawning normally occurs beneath the nest in an 'embrace' typical of osphronemids, with the male wrapped around the female.

At the point of climax milt and a few eggs are released in a cluster or 'packet', which the male collects and transports to the nest. The process is then repeated until the female is spent, with 1-200 eggs typically deposited.

Post-spawning the adults can normally be left in situ. The female is normally tolerated by the male and may even play an active role in defending the area around the nest from intruders.

The eggs normally hatch within 48 hours with the fry remaining in the nest for 3-4 additional days, until the yolk sac is fully-absorbed. When the fry begin to swim freely the male will lose interest, and adults or fry can then be removed.

They require an infusoria-grade food for the first few days, after which they can accept motile foods such as microworm and Artemia nauplii. Water changes should be small and regular rather than large and intermittent.

Notes

This species can be distinguished from congeners by its larger adult size, more-extended filamentous anal-fin rays extending almost to the tip of the caudal-fin (vs. not extending past the middle of the caudal-fin), tendency to possess 3 (vs- 1-2) dark lateral stripes on the body, and typical presence (vs. absence) of a dark spot above the pectoral-fin. Wild populations vary in colour pattern to an extent, and it is possible that there is hidden diversity within the genus.

The common name is derived from the ability of genus members to produce audible sounds via a specialised pectoral mechanism which is unique within the family Osphronemidae. The structure comprises modified pectoral-fin tendons and muscles which are stretched and plucked by the basal portion of the anterior fin rays in a similar way to guitar strings. The pectoral-fins beat alternately, each able to generate short or long bursts of sound. These sounds are produced by both sexes, predominantly during agnostic and nuptial interactions, and they differ in temporal parameters, frequency, and pressure between the species. Studies suggest that Trichopsis species are able to settle conflicts without damaging each other physically by assessing factors such as body weight and length, which are transmitted by both visual and acoustic 'croaking' signals. During courtship the female produces 'purring' sounds in order to initiate spawning, and they are the only fishes in which this is known to occur.

Following Rainboth (1996), the genus Trichopsis can be diagnosed as follows: dorsal-fin origin markedly posterior to pectoral-fin base; pelvic-fin with a single spinous ray with a filamentous extension, and 4 branched rays; 2-4 spinous dorsal-fin rays; 4-8 spinous anal-fin rays; lateral line absent. Its closest relatives are considered to be the genera Betta and Pseudosphromenus.

Like others in the suborder Anabantoidei this species possesses an accessory breathing organ known as the labyrinth, which permits the fish to breathe atmospheric air to a certain extent. Comprising paired suprabranchial organs formed via expansion of the epibranchial (upper) section of the first gill arch and housed in a chamber above the gills, it contains many highly-vascularised, folded flaps of skin which function as a large respiratory surface. Its structure varies in complexity between species, tending to be more developed in those inhabiting harsher environments.

References

  1. Schofield, P. J. and D. J. Pecora (2013). Croaking gourami, Trichopsis vittata (Cuvier, 1831), in Florida, USA. BioInvasions Records 2(3), 247-251
  2. Cuvier, G. and A. Valenciennes. (1831). Histoire naturelle des poissons. Tome septième. Livre septième. Des Squamipennes. Livre huitième. Des poissons à pharyngiens labyrinthiformes. Histoire naturelle des poissons. v. 7, 1-531
  3. Kottelat, M. (2013). The fishes of the inland waters of southeast Asia: a catalogue and core bibiography of the fishes known to occur in freshwaters, mangroves and estuaries. The Raffles Bulletin of Zoology Supplement 27, 1-663
  4. Knight, J. D. M. and S. Balasubramanian (2015). On a Record of Two Alien Fish Species (Teleostei: Osphronemidae) from the Natural Waters of Chennai, Tamil Nadu, India. Journal of Threatened Taxa 7(3), 7044-7046
  5. Bischof, C. (1996). Diversity in Agonistic Behavior of Croaking Gouramis (Trichopsis vittata, T. schalleri, and T. pumila; Anabantoidei) and the Paradise Fish (Macropodus opercularis; Anabantoidei). Aggressive Behavior 22, 447-455
  6. Ladich, F. and G. Schleinzer (2015). Effect of temperature on acoustic communication: Sound production in the croaking gourami (labyrinth fishes). Comparative Biochemistry and Physiology, Part A 182, 8-13
  7. Ladich, F. (1998). Sound Characteristics and Outcome of Contests in Male Croaking Gouramis (Teleostei). Ethology 104, 517-529
  8. Ladich, F. (2007). Females whisper briefly during sex: context- and sex-specific differences in sounds made by croaking gouramis. Animal Behaviour 73(2), 379-387
  9. Rüber, L, R. Britz and R. Zardoya (2006). Molecular phylogenetics and evolutionary diversification of labyrinth fishes (Perciformes: Anabantoidei). Systematic Biology 55(3), 374-397
  10. Linke, H. (1992). Labyrinth Fish: The Bubble Nest Builders. Tetra Press, 1-176
  11. Roberts, T. R. (1993). The freshwater fishes of Java, as observed by Kuhl and van Hasselt in 1820-23. Zoologische Verhandelingen (Leiden) 285, 1-94
  12. Ng, H. H. and H.-H. Tan (1999). The fishes of the Endau drainage, Peninsular Malaysia with descriptions of two new species of catfishes (Teleostei: Akysidae, Bagridae). Zoological Studies 38(3), 350-366
  13. Rainboth, W. J. (1996). FAO species identification field guide for fishery purposes. Fishes of the Cambodian Mekong. Rome, FAO, 1-265
  14. Freyhof, J., D. V. Serov and T. N. Nguyen (2000). A preliminary checklist of the freshwater fishes of the River Dong Nai, South Vietnam. Bonner Zoologische Beiträge 49(1-4), 93-99
  15. Kottelat, M. (2001). Fishes of Laos. WHT Publications, Colombo, 1-198
  16. Tan, H. H. and P. K. L. Ng (2005). The labyrinth fishes (Teleostei: Anabanatoidei, Channoidei) of Sumatra, Indonesia. Raffles Bulletin of Zoology Supplement 13, 115-138
  17. Kottelat, M. (1998). Fishes of the Nam Theun and Xe Bangfai basins, Laos, with diagnoses of twenty-two new species (Teleostei: Cyprinidae, Balitoridae, Cobitidae, Coiidae and Odontobutidae). Ichthyological Exploration of Freshwaters 9(1), 1-128

Distribution

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Missing: water condition notes.