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Paracanthocobitis zonalternans (BLYTH, 1860)

SynonymsTop ↑

Cobitis zonalternans Blyth, 1860; Nemacheilus zonalternans (Blyth, 1860); Noemacheilus zonalternans (Blyth, 1860); Acanthocobitis zonalternans (Blyth, 1860); Noemacheilus phuketensis Klausewitz, 1957; Nemacheilus phuketensis Klausewitz, 1957; Acanthocobitis phuketensis Banarescu and Nalbant, 1964

? Cobitis chlorosoma (McClelland 1839) or Acanthocobitis chlorosoma (McClelland 1839) [Kottelat, 2012b & 2013]

Etymology

Paracanthocobitis: from the Greek παρά (para), meaning ‘close beside,’ and the genus Acanthocobitis from the Greek ἄκανθος ‎(ákanthos), meaning ‘thorned’, in reference to the spine beneath the eye in the type species [originally A. longipinnis, now A. pavonacea], and κωβιός ‎(kōbiós), meaning ‘a kind of small fish’.

Classification

Order: Cypriniformes Family: Nemacheilidae

Distribution

This species’ known  range extends southwards from the Indian state of Manipur (Brahmaputra River system) through Myanmar (including the Chindwin, Ayeyarwady, Sittaung and Salween River drainages), into western and peninsular Thailand (including the Mae Klong and Tapi Rivers) and possibly mainland Peninsular Malaysia (it was recorded from the Langkawi Islands off the country’s western coastline during surveys for a study published in 2006).

Kottelat (1990) designated a neotype from ‘Huai Mae Charno, 4 kilometers south of Amphoe Mae Ramat on road 1085, 16°58’N, 98°34’E, Tak Province, Salween basin, Thailand’.

Patterning and colouration differs somewhat depending on locality; the central body stripe, for example, can be completely solid or reduced to a series of blotches.

Habitat

Recorded to inhabit a range of biotopes from headwaters to larger river channels and is said to show a preference for shallow riffles with pebbly substrates (Kottelat, 1990).

Most habitats images we’ve seen depict clear, flowing water with complex submerged structures of rocks or tree roots.

At the neotype locality a number of other species were recorded including Homaloptera bilineata, Homalopteroides modesta, Schistura moeiensis, S. paucicincta, Lepidocephalichthys berdmorei, L. hasselti, Pangio pangia, Pethia ticto, Esomus metallicus, Rasbora daniconius, and Trichopsis vittata.

Another diverse locality further south at Ban Khlong Sok in Surat Thani Province yielded over 40 species including Homalopteroides smithi, Homaloptera ogilviei, Schistura geisleri, Amblyceps mangois and Akysis hendricksoni.

At an unnamed stream in Mon State, southern Myanmar the water was clear, greenish and flowing slowly with no natural shade. There was no marginal or submerged vegetation and the substrate was composed of mud and sand.

A. zonalternans was collected in a depth of 0.3-0.5 metres alongside Pethia stoliczkana, Rasbora daniconius plus unidentified species of Lepidocephalichthys, Glossogobius and Channa.

Maximum Standard Length

70 – 78 mm.

Aquarium SizeTop ↑

A tank with base dimensions of 60 ∗ 30 cm is big enough to house a small group.

Maintenance

Will do well in most well-maintained aquaria provided sufficient cover is available, and should not harm softer-leaved plants. However we recommend keeping it in a set-up designed to resemble a slow-moving or marginal section of stream or river with a sandy substrate and perhaps a few water-worn boulders.

This can be further decorated with driftwood roots and branches arranged to form some shaded spots, plus a few handfuls of dried beech, oak or Terminalia (Indian Almond) leaves.

Adaptable plants such as MicrosorumBolbitis or Anubias spp. can be grown attached to the décor and bright lighting will promote the growth of aufwuchs which will add to the natural feel.

In this kind of environment the fish will show more natural behaviour and can be maintained alongside other species that enjoy similar conditions.

Although a high level of water movement isn’t essential it’s also proven to thrive in a mature hill stream-type set-up with a rocky aquascape. Weekly water changes of 30-50% tank volume should be considered routine.

Water Conditions

Temperature: 20 – 25 °C

pH: 6.0 – 7.5

Hardness: 36 – 179 ppm

Diet

Probably a micropredator feeding on insect larvae and suchlike in nature.  Singer and Page (2015) report that stomach contents examined during their study were larval chironomids and ephemeropterans.

In the aquarium it will accept sinking dried foods but should also be offered regular meals of small live and frozen fare such as Daphnia, Artemia, bloodworm, etc. A varied diet is the key to maintaining it in the best of health.

Behaviour and CompatibilityTop ↑

Among the more peaceful members of the genus and an excellent addition to communities of small, stream-dwelling fishes.

Good tankmates include peaceful schooling or shoaling cyprinids plus rheophilic loaches such as Gastromyzon, Pseudogastromyzon, Beaufortia or Sewellia spp., and less territorial nemacheilids.

Stream-dwelling gobies from genera including Sicyopterus, Stiphodon, Rhinogobius and Lentipes can also make interesting additions to this kind of communityTerritorial or otherwise aggressive bottom-dwellers are less suitable companions.

It does best in the presence of conspecifics and should be kept in a mixed sex group comprising at least half a dozen specimens, preferably 10 or more.

This will allow you to observe some interesting social interactions and the formation of a hierarchy between males. While rivals can be aggressive towards one another this shouldn’t become problematic in a well-structured set-up.

Sexual Dimorphism

Dominant males of some populations develop yellow to reddish orange colouration in the finnage, around the mouthparts and sometimes in the anterior portion of the body. All males possess a suborbital flap with pectoral fin rays 2-6 thickened and covered in tubercules.

Adult females lack these characters and tend to be slightly larger and fuller-bodied.

Reproduction

Several successes have now been recorded but the first was by UK aquarist Mick Wright who obtained his specimens from fellow fishkeeper Andy Rushworth.

Andy had recovered a small number of fry from one of his filters and repeatedly observed spawning behaviour in his wild caught adults, but it appeared that most of the eggs were being consumed.

To remedy this Mick used a small, 30 cm x 15 cm aquarium, to the base of which was added plastic under-gravel filter plates with the central, slatted sections removed and replaced with 1mm diameter mesh. On top of this was placed a double layer of glass marbles and an air-powered sponge filter was installed (see photo).

Initially a pair of males and three females were added but aggression between the males proved too intense so one was removed and the remaining fish left in the spawning tank overnight before being removed. 98  fry were subsequently raised from this first attempt with no particular trigger required to induce breeding activity as the fish were already spawning on a daily basis in the stock tank.

The eggs hatched in around 24-36 hours with fry free swimming within three days. At this point they were fed Paramecium until large enough to accept Artemia nauplii.

Later, chopped Tubifex, grindal worm and crushed flake were introduced to the diet. Subsequent experiences by other hobbyists have shown that this species is prolific for a small fish with up to 300 eggs being deposited in a single spawning event.

NotesTop ↑

Paracanthocobitis zonalternans differs from all other species of Paracanthocobitis by the combination of incomplete lateral line ending before or near dorsal-fin origin; axillary pelvic lobe present; wide interorbital space, mean = 36% HL.

The lateral line is incomplete in this species, a trait also found in P. mooreh and P. linypha, but these two species do not have the axillary pelvic lobe present in P. zonalterans.

According to Kottelat (2012b), several species are confused under the name of the subject species.   Singer & Page (2015) surmise that given the large geographic distribution, habitat variation, variability of colour pattern across geographic ranges, and morphometric differences, it is likely that P. zonalternans is a species complex.

The genus Acanthocobitis was described by Peters (1861) with Acanthocobitis longipinnis designated as the type species.  The placement and status of this species was questioned by several authors beginning with Menon (1987) who considered it a junior synonym of Cobitis botia Hamilton, 1822.  Grant (2007) compared the holotype of A. longipinnis with live specimens of A. botia and found the two species to be easily distinguished.  He noted that A. longipinnis is distinguished from all other Acanthocobitis species in having a pointed caudal fin, vertically oriented suborbital flap, slender body, long dorsal fin, anus closer to anal-fin insertion than to pelvic-fin insertion, and greenish colouration.

Grant (2007) considered Acanthocobitis longipinnis to be a junior synonym of A. pavonacea and proposed the subgenus Paracanthocobitis (type species C. zonalternans) to include all other species since he regarded A. pavonacea to be taxonomically unique.  Kottelat (2012a) remarked that the identity of A. longipinnis required verification and later (Kottelat, 2012b) classed Paracanthocobitis as a questionable synonym of Acanthocobitis.

Singer and Page (2015) recognize Paracanthocobitis as a genus, differing from Acanthocobitis as diagnosed by Grant (2007, 2008), although the two genera are most likely sister taxa based on the unique papillated pad on either side of a medial interruption on the lower lip.  Fourteen species including five new species described therein are assigned to Paracanthocobitis, with Acanthocobitis treated as monotypic, containing only A. pavonacea, a species restricted to the Brahmaputra and Ganges river basins of northern India and Bangladesh.  Acanthocobitis longipinnis is considered to be a synonym of A. pavonacea (Grant, 2007); however, the only available specimen of A. longpinnis is the poorly preserved holotype.  Collection of fresh material may show the two forms to be distinguishable from one another.  [Singer and Page, 2015, p. 398]

Paracanthocobitis is distinguished from all other genera in the family by the combination of lower lip with a large papillated pad on either side of a medial interruption; upper lip with 2–5 rows of papillae and continuous with lower lip; conspicuous black spot with white outline (an ocellus) on upper half of caudal-fin base.

Paracanthocobitis is distinguished from Acanthocobitis in having an emarginate or truncate (vs. pointed) caudal fin; 9 and 1/2 –15 and 1/2 (vs. 17 and 1/2 –19 and 1/2) branched dorsal-fin rays; rounded (vs. more triangular-shaped) head in lateral view; horizontally (vs. vertically) oriented suborbital flap or groove; papillated pad on either side of narrow (vs. wide) medial interruption in lower lip; anus closer to pelvic-fin insertion than to anal-fin insertion (vs. closer to anal-fin insertion).  [Singer and Page, 2015, p. 380]

The family Nemacheilidae is widely-distributed across most of Eurasia with the Indian subcontinent, Southeast Asia and China representing particular centres of species diversity.

References

  1. Ahmad, A. and K. K. P. Lim, 2006 - Malayan Nature Journal 59: 103–120
    Inland fishes recorded from the Langkawi Islands, Peninsular Malaysia.
  2. Grant, S., 2008 - BSSW-Report 20(3): 49-52
    Schmerlen der Gattung Acanthocobitis Peters, 1861.
  3. Grant, S., 2007 - Ichthyofile No. 2: 1-9
    A new subgenus of Acanthocobitis Peters, 1861 (Teleostei: Nemacheilidae).
  4. Kottelat, M., 2013 - Raffles Bulletin of Zoology Supplement No. 27: 1-663
    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.
  5. Kottelat, M., 2012b - Raffles Bulletin of Zoology Supplement 26: 1-199
    Conspectus cobitidum: an inventory of the loaches of the world (Teleostei: Cypriniformes: Cobitoidei).
  6. Kottelat, M., 2012a - Zootaxa 3327: 45-52
    Acanthocobitis pictilis, a new species of loach from Myanmar and Thailand (Teleostei: Nemacheilidae).
  7. Kottelat, M., 1990 - Verlag Dr. Friedrich Pfeil, München, Germany: 1-262
    Indochinese nemacheilines. A revision of nemacheiline loaches (Pisces: Cypriniformes) of Thailand, Burma, Laos, Cambodia and southern Viet Nam.
  8. Singer, R. A. and L. M. Page, 2015 - Copeia v. 103 (no 2): 378-401
    Revision of the zipper loaches, Acanthocobitis and Paracanthocobitis (Teleostei: Nemacheilidae), with descriptions of five new species.
  9. Tang, Q., H. Liu, R. Mayden and B. Xiong, 2006 - Molecular Phylogenetics and Evolution 39(2): 347-357
    Comparison of evolutionary rates in the mitochondrial DNA cytochrome b gene and control region and their implications for phylogeny of the Cobitoidea (Teleostei: Cypriniformes).

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