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Opsarius bernatziki

(Koumans, 1937)Formerly Barilius bernatziki Koumans, 1937

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This species is very rare in the aquarium hobby.
This species is very rare in the aquarium hobby.Nonn Panitvong/Siamensis.org

Quick factsEdit

Max size
90mm SL3.5in SL
Aquarium size
120 × 45cm48 × 18in
Temp
18–26°C64–79°F
pH
6.0–7.5
Hardness
2–12dGH

Difficulty6 of 8 measures

Moderate

How the rating is worked out

Space
large tank
Water
flexible
Temp
flexible
Diet
unknown
Temperament
unknown
Social
needs to be in a group
Compatibility
choose tankmates carefully

Other demands

Each of these can raise the rating on its own, whatever the measures above say.

Hardiness
needs a well-established tank

Before you buy

  • Needs a tight-fitting lid as this species is known to jump

    A tightly-fitting cover is also essential as Opsarius spp.

Sold as 'blue hillstream trout', Opsarius bernatziki is a cyprinid from peninsular Thailand and Tanintharyi, Myanmar, south of the Isthmus of Kra. It inhabits well-oxygenated, moderate to fast-flowing rivers and streams, usually 10-20 km or more from the sea. Six or seven bluish vertical bars on each flank and a large blotch at the caudal-fin base help identify it. Like its congeners it is too fast and vigorous a feeder for the general community.

Etymology

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Opsarius: apparently from an Ancient Greek word meaning 'small fish'.

bernatziki: named for Dr. H. Bernatzik who collected the type series in 1936 and 1937.

Distribution

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The precise extent of this species' distribution is unclear. It appears to occur in river systems on both sides of the Tennaserim Hills in Ranong, Phang-nga and Pattani provinces in peninsular Thailand, plus Tanintharyi (formerly Tennaserim) Division, Myanmar, all located south of the Isthmus of Kra.

Type locality is 'Kapa, northwestern peninsular Thailand', which may refer to modern-day Kapoe district in Ranong province.

Inhabits well-oxygenated, moderate to fast-flowing rivers and streams with substrates of gravel, cobbles, larger boulders and exposed bedrock, and is absent in coastal drainages tending only to be found 10-20 km or more away from the sea.

In the Sai Buri river, Pattani province, southern Thailand it was collected from a stretch less than 2 metres deep with a muddy bed and sandy margins alongside Nemacheilus masyai, Tuberoschistura baenzigeri, Balitoropsis zollingeri, Acantopsis sp., Labiobarbus lineatus, Cyclocheilichthys heteronema, Mystacoleucus chilopterus, Mystus nigriceps, Xenentodon cancila, Glossogobius giuris and Brachirus harmandi.

Aquarium size

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Standard length
90mm SL3.5in SL
Aquarium base
120 × 45cm48 × 18in
Volume
~243litres~64US gal

An aquarium with minimum surface area of 120 ∗ 45 cm48 ∗ 18 in or equivalent should be the smallest considered.

Maintenance

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The aquarium should ideally be designed to resemble a flowing stream or river with a substrate of variably-sized rocks, sand, fine gravel, and some larger water-worn boulders. This can be further furnished with driftwood roots and branches if you wish but be sure to leave plenty of open swimming space.

While the majority of aquatic plants will fail to thrive in such surroundings hardy genera such as Microsorum, Bolbitis, or Anubias spp. can be grown attached to the décor.

This species is intolerant to the accumulation of organic wastes and requires spotless water at all times in order to thrive. It also does best if there is a high proportion of dissolved oxygen and moderate degree of water movement meaning external filters, powerheads, airstones, etc., should be employed as necessary.

As stable water conditions are obligatory for its well-being this fish should never be added to biologically-immature aquaria, and weekly water changes of 30-50% aquarium volume should be considered mandatory. A tightly-fitting cover is also essential as Opsarius spp. are prodigious jumpers.

Water conditions

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Temperature
18–26°C64–79°F
pH
6.0–7.5
Hardness
2–12dGH

These recommendations come from this profile’s own figures. They contain affiliate links, so we may earn a commission.

Opsarius spp. are predominantly surface-feeders preying on aquatic and terrestrial insects in nature, with some small fishes and benthic invertebrates probably taken as well.

In the aquarium good quality dried products can be offered but should be supplemented with regular meals of live and frozen fare such as chironomid larvae (bloodworm), Artemia, chopped earthworms, etc. Drosophila fruit flies and small crickets are also suitable provided they are gut-loaded prior to use.

Behaviour and compatibility

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Unsuitable for the general community due to its environmental requirements, and likely to outcompete or intimidate slow-moving and less bold species at meal times since it is an extremely fast swimmer and vigorous feeder. Much smaller fishes should also be omitted as they may be predated upon.

The best tankmates are similarly-sized, robust, pelagic cyprinids such as Dawkinsia, Barilius or larger Devario and Rasbora spp. while bottom-dwellers could consist of Garra, Crossocheilus, Botia and Schistura spp., for example. Many characids and loricariid catfishes should also work well, but be sure to perform thorough research before purchase.

Although gregarious by nature this is a shoaling rather than schooling species which develops a distinct pecking order and therefore should always be maintained in a group of five or more individuals. If only two or three are purchased the subdominant fish may be bullied incessantly whereas solitary specimens may become aggressive towards similar-looking species

Sexual dimorphism

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Adult females are less-brightly-coloured, tend to grow a little larger and are thicker-bodied than males, especially when gravid.

Nuptial males develop orange pigmentation in the lower portion of the body.

Reproduction

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Unreported.

Notes

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This species is occasionally available in the ornamental trade and is normally sold as 'blue hillstream trout'.

It possesses 6-7 bluish vertical bars on each flank and a similarly-coloured, relatively large blotch at the base of the caudal-fin, plus very short pairs of rostral and maxillary barbels.

O. dogarsinghi and O. signicaudus are the only two Southeast Asian congeners to possess a large blotch at the caudal-fin base but in the former the blotch is vertically-orientated and hardly extends onto the fin itself (vs. laterally-elongate and extending onto the basal fin rays in some specimens of O. bernatziki) and long (vs. short) barbels, while the latter has 36-39 (vs. 33 or less) scales in the lateral row.

The generic placement of species currently referred to Opsarius has been open to question since Howes (1980) concluded that the Barilius grouping, within which they were included at the time, was not monophyletic and identified two separate lineages. The first group contained B. barila, the type species, plus B. bendelisis, B. radiolatus, B. vagra, and B. shacra, while the second included all other species, and initially these were referred to the subdivisions 'group i' and 'group ii' within Barilius itself.

The composition of these groups is confusing since in a later work Howes (1983) included B. evezardi and B. modestus in 'group i' whilst omitting B. bendelisis, B. radiolatus, and B. shacra without explicitly stating why.

Rainboth (1991) assigned the members of Howe's 'group ii' to the revalidated generic name Opsarius based on the fact it was the oldest available with 'group i' species retaining the name Barilius due to the presence of the type species.

This system has been followed by some subsequent authors, e.g., Tang et al. (2010) and Collins et al. (2012) but not gain wider usage until Kottelat (2013), who included all former Barilius from Southeast Asia in Opsarius.

References

  1. Koumans, F. P. (1937). On a collection of fishes from Siam. Zoologische Mededelingen (Leiden) 20, 61-64
  2. Nath, P., D. Dam, and A. Kumar (2010). A New Fish Species of the Genus Barilius (Cyprinidae: Rasborinae) from River Siang, D'Ering Memorial Wildlife Sanctuary, Arunachal Pradesh, India. Records of the Zoological Survey of India 110(3), 19-33doi.org/10.26515/rzsi/v110/i3/2010/158930
  3. Howes, G. J. (1980). The anatomy, phylogeny and classification of bariliine cyprinid fishes. Bulletin of the British Museum (Natural History) : Zoology series 37(3), 129-198
  4. Liao, T-Y, S. O. Kullander, and F. Fang (2011). Phylogenetic position of rasborin cyprinids and monophyly of major lineages among the Danioninae, based on morphological characters (Cypriniformes: Cyprinidae). Journal of Zoological Systematics and Evolutionary Research 49(3), 224-232
  5. Tang, K. L., M. K. Agnew, W. J. Chen., M. V. Hirt, T. Sado, L. M. Schneider, J. Freyhof, Z. Sulaiman, E. Swartz, C. Vidthayanon, M. Miya, K. Saitoh, A. M. Simons, R. M. Wood and R. L. Mayden (2010). Systematics of the subfamily Danioninae (Teleostei: Cypriniformes: Cyprinidae). Molecular Phylogenetics and Evolution 57(1), 189-214
  6. Collins R. A., K. F. Armstrong, R. Meier, Y. Yi, S. D. J. Brown, R. H. Cruickshank, S. Keeling, and C. Johnston (2012). Barcoding and border biosecurity: identifying cyprinid fishes in the aquarium trade. PLoS ONE 7(1), e28381
  7. Tejavej, A. (2012). Barilius signicaudus, a new species of cyprinid fish from Maeklong Basin, western Thailand (Cypriniformes: Cyprinidae). Zootaxa 3586, 138-147
  8. 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

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