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Rhaphiodon vulpinus SPIX & AGASSIZ, 1829

Biara

SynonymsTop ↑

Hydropardus rapax Reinhardt, 1849; Salmo tamuco Kner, 1860

Etymology

Rhaphiodon: from the Greek rhaphis, meaning ‘needle’, and odous, meaning ‘tooth’.

vulpinus: from the Latin vulpinus, meaning ‘fox’.

Classification

Order: Characiformes Family: Cynodontidae

Distribution

R. vulpinus is the most widely-distributed member of the family Cynodontidae.

Type locality is given simply as ‘Brazilian rivers’, but this species is currently understood to be distributed in the Amazon basin from the Río Ucayali system in Peru, eastward as far as the rio Xingu in Brazil, plus the rio Tocantins and Rio Capim basins.

It’s also known from the Río Orinoco basin in Venezuela, Rupununi drainage in the upper Essequibo River system in Guyana, and the Rio Paraná/Paraguay and Río Uruguay basins in Paraguay and Uruguay with the Río de la Plata in Argentina representing its southern limit.

It exhibits a degree of morphological and phenotypic variation with specimens from the upper Xingu possessing a greater number of lateral line scales and branched anal-fin rays than those from elsewhere while those from the rio Negro tend to be more brownish in colour, for example.

Habitat

Occurs in both main river channels and some reservoirs, with fluvial populations undergoing annual reproductive migrations.

Maximum Standard Length

600 – 800 mm.

Aquarium SizeTop ↑

Suitable only for public installations or the very largest private aquaria.

Maintenance

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.

Like many fishes that naturally inhabit running waters it’s 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 so 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 essential as this species is a prodigious jumper, and it may also prove beneficial to cover the back and sides of the aquarium in order to reduce the chances of it swimming into the glass since it can be skittish, especially in confined surroundings.

Water Conditions

Temperature24 – 28 °C

pH6.0 – 8.0

Hardness36 – 268 ppm

Diet

An obligate but generalised piscivore capable of consuming surprisingly large prey.

Newly-imported specimens often refuse to accept anything but live fishes but most can be weaned onto dead alternatives once recognised as edible.

Like the vast majority of predatory fishes this species should not be fed mammalian or avian meat like beef heart or chicken, and similarly there is no benefit in the long-term use of ‘feeder’ fish such as livebearers or small goldfish which carry with them the risk of parasite or disease introduction and at any rate tend not have a high nutritional value unless properly conditioned beforehand.

Behaviour and CompatibilityTop ↑

Best kept alone, or with similarly-sized, non-aggressive fishes it cannot fit into its mouth since it’s otherwise quite peaceful and easily-dominated.

It can also be maintained in a group in a suitably-sized aquarium but the purchase of at least three specimens is advisable.

Reproduction

This species is reproductively active between the months of September/October to January/April, this period coinciding with high water levels across much of its range.

It’s thus referred to as possessing a seasonal reproductive strategy with the beginning of the cycle associated with the flood regime of its native rivers, and the fish migrating into inundated areas to spawn.

As far as we know it’s never been bred in aquaria.

NotesTop ↑

R. vulpinus is currently the only member of its genus and probably should not be considered a home aquarium subject at all given its eventual size and natural behaviour.

We know of only a handful of private aquarists with the facilities required to house it long-term.

Unfortunately, juveniles are seen for sale quite regularly, most often without adequate information regarding their long-term care, and it’s common to see them being maintained in medium-sized aquaria with no possibility of achieving their potential.

Other vernacular names include ‘vampire barracuda’, ‘Chambira-challua’ (Peru), ‘Payara-machete’ or ‘Payarin’ (Venezuela) and ‘Pirayagua’ (araguay).

In Brazil it’s known by various names including ‘Chafalote’, ‘Dentudo’, ‘Peixe-cachorro’, ‘Peixe-cadela’, ‘Ripa’ and ‘Saranha’ as well as the most common ‘Biara’.

Rhaphiodon can be told apart from other genera in the family Cynodontidae by the following characters: dorsal-fin located on the posterior third of the body (predorsal distance 69.3–74.4 % SL, vs. 52.2–61.1 % of SL in all other species); body very elongate (body depth at dorsal-fin origin 12.7–19.6 % SL, vs. 19.1–33.7 %); 62-68 vertebrae (vs. 44–54).

It’s further distinguished from Hydrolycus spp. by the dorsal-fin insertion being located slightly posterior to a vertical through the anal-fin origin (vs. distinctly anterior) and from Cynodon by possession of 38–50 anal-fin rays (vs. 61-80).

It’s sometimes included in the putative subfamily Cynodontinae alongside Cynodon and Hydrolycus, these being separated from other Characiformes by a series of derived features plus their oblique mouth shape and highly-developed dentary canine teeth.

The latter fit into a pair of corresponding openings in the upper jaw which allows the mouth to be closed completely.

Cynodontinae contains two primary monophyletic lineages, one comprising the genus Hydrolycus and the other a clade with Cynodon and Rhaphiodon spp., with members sometimes referred to collectively as ‘dogtooth characins’.

References

  1. Reis, R. E., S. O. Kullander and C. J. Ferraris, Jr. (eds.), 2003 - EDIPUCRS, Porto Alegre: i-xi + 1-729
    Check list of the freshwater fishes of South and Central America. CLOFFSCA.
  2. Reuberger, A. L., E. E. Marques, C. S. Agostinho and R. J. de Oliveira , 2007 - Neotropical Ichthyology 5(4): 479-484
    Reproductive biology of Rhaphiodon vulpinus (Ostariophysi: Cynodontidae) in the Tocantins River Basin, Brazil.
  3. Toledo-Piza, M., 2000 - American Museum Novitates 3286: 1-88
    The Neotropical Fish Subfamily Cynodontinae (Teleostei: Ostariophysi: Characiformes): A Phylogenetic Study and a Revision of Cynodon and Rhaphiodon.
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