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Brachydanio sp. 'hikari'

Hikari 'Danio'

Etymology

Brachydanio: from the Ancient Greek βραχύς (brakhús), meaning ‘short’, and Dhani, a Bengalese vernacular term for small, minnow-like cyprinids.

Classification

Order: Cypriniformes Family: Cyprinidae

Distribution

Collected from the Tanintharyi River drainage, a tributary of the Tenasserim River system in Tanintharyi (formerly Tenasserim) Division, southern Myanmar.

Habitat

No details are available but expect it to inhabit quieter, slower-moving sections of streams and minor rivers.

Maximum Standard Length

55 – 65 mm.

Aquarium SizeTop ↑

An aquarium with base dimensions of 120 ∗ 30 cm or equivalent should be the smallest considered.

Maintenance

Looks particularly effective in a heavily-planted arrangement with a darker substrate, and may appear paler in sparsely-decorated set-ups.

We suggest maintaining it in a well-planted aquarium or set-up designed to resemble a flowing river or stream, with a substrate of variably-sized rocks and gravel and some large water-worn boulders.

Additional powerhead(s) or filter outlets can be used to provide flow but torrent-like conditions should be avoided since small danionins tend to occupy calmer stretches and marginal zones in nature.

Driftwood roots, branches and aquatic plants, with hardy genera such as Microsorum, Bolbitis or Anubias ideal since they can be grown attached to the décor, can also be added.

The aquarium must have a very tightly-fitting cover as members of this genus are accomplished jumpers and can fit through surprisingly small gaps.

Water Conditions

Temperature18 – 26 °C

pH6.5 – 7.5

Hardness18 – 215 ppm

Diet

Probably preys on insects and their larvae in nature. In the aquarium it’s largely an unfussy feeder and will accept most foods.

A good quality dried product or two can be used as the staple diet but this should be supplemented with regular meals of small live and frozen fare such as bloodwormDaphniaArtemia, etc. for the fish to show the best colouration and conditioning.

Behaviour and CompatibilityTop ↑

This species is very peaceful indeed making it an ideal resident of the well-furnished community tank.

Since it places no special demands in terms of water chemistry it can be combined with many of the most popular fish in the hobby including other small cyprinids as well as tetras, livebearers, rainbowfishes, anabantoids, catfishes and loaches, though its adult size must be taken into consideration.

It’s a schooling species by nature and really should be kept in a group of at least 8-10 specimens.

Maintaining it in decent numbers will not only make the fish less nervous but result in a more effective, natural-looking display while males will also exhibit their best colours as they compete with one other for female attention.

Sexual Dimorphism

Males have an overall yellowish-green body colour which extends into the fins whereas females are predominantly blue.

Reproduction

Like most cyprinids this species is an egg-scattering spawner that exhibits no parental care.

That is to say when the fish are in good condition they will spawn often and in a densely-planted, mature aquarium it is possible that small numbers of fry may start to appear without human intervention.

However if you want to increase the yield of fry a slightly more controlled approach is required.

The adult group can still be conditioned together but one or more small, say 30-40 litre, containers should also be set up and half-filled with water.

Much of the available space should be filled with a suitable spawning medium such as Java moss, wool mops or a spawning grid.

The water should be of slightly acidic to neutral pH with a temperature towards the upper end of the range suggested above.

An internal power filter can be added initially and this should be positioned so that the flow is directed down the full length of the tank.

When the adult fish are well-conditioned and the females appear full of eggs one or two pairs should then be introduced to each container.

Spawning can be initiated by adding small amounts of cool water every few hours in such a way that the tank is gradually topped up and feeding small amounts of live and frozen foods, or by performing a large (50-60%) water change in the evening.

Several spawning events will probably occur before a female is spent of eggs.

The adults will eat any they find and are best removed once eggs are spotted.

At this point the power filter (if using) should be switched for a mature sponge-type unit in order to avoid fry being sucked into the mechanism.

Incubation in is temperature-dependant to an extent but usually takes between 24-36 hours with the young free-swimming a few days later.

Initial food should be Artemia nauplii or similar.

NotesTop ↑

This probable undescribed species first became available to aquarists in 2002, with males and females marketed as ‘Danio sp. hikari yellow’ and ‘D. sp. hikari blue’, respectively.

Subsequent DNA testing in the United States revealed them to be the same species and genetically distinct from the very similar B. kerri.

It can be told apart as the central body (P) stripe always extends into the caudal-fin whereas in B. kerri it terminates at the caudal peduncle.

Only a single population of B. kerri was sampled in the study meaning this could still turn out to be a particularly colourful form of that species, however.

In recent years it’s become commonplace to refer to the stripes on the body and fins of danionins as follows:

– P stripe: or “pigment stripe” is the central, dark, lateral stripe on the body which extends into the caudal-fin in some species. Stripes above it are numbered P+1, P+2, etc. and those beneath P-1, P-2, P-3.
– A stripe: the central stripe on the anal-fin; the proximal stripe (above it) is A+1 and the distal stripe (beneath) A-1.
– D stripe: The submarginal dorsal-fin stripe.

Following Fang (2003) Brachydanio spp. are characterised by the presence of an A stripe on the anal-fin and two or more P stripes on the caudal, plus some internal characteristics such as enlarged nasal lamellae.

The genus has undergone some significant taxonomic reshuffling in recent years following the publication of a series of phylogenetic studies.

Older, molecular, phylogenies tended to agree that it represented a monophyletic group consisting of two major clades; the ‘Danio devario‘ group containing the larger, deeper-bodied species and the ‘D. rerio‘ clade comprising the smaller, slimmer fish.

However in 2003 Fang conducted a more detailed study based on morphological characters which included members of other related genera, and the results suggested for the first time that the genus Danio as previously considered represents a polyphyletic grouping, i.e., not all members derived from a single common ancestor.

The genus name Devario was suggested for the larger species with Danio being applied only to the smaller fish (with the exception of the type species, D. dangila which can grow to around 89 mm SL). Recent molecular studies by Mayden et al. (2007) and Fang et al. (2009) resulted in further changes, with the latter study considering the genus Danio to be composed of three subclades. These were subsequently split into distinct genera by Kottelat (2013), as follows:

The former species D. erythromicronD. margaritatusD. choprae and D. flagrans are grouped together in the revalidated genus Celestichthys Roberts, 2007. These exhibit unique body patterning consisting of vertical bars (C. erythromicronC. chopraeC. flagrans) or light spots (C. margaritatus) and possess either very short barbels or none at all.

The genus Danio contains only the type species, D. dangila, separated on the basis of its larger size and the shape of the caudal-fin, which in adults is only slightly emarginate or even truncate in shape, a feature it shares only with Tinca tinca (the common tench) among other cyprinids.

The remaining species, of which B. rerio is thought to be the most ancient, are included in the revalidated genus Brachydanio Weber & de Beaufort, 1916.

References

  1. Conway, K.W., W.-J. Chen and R.L. Mayden, 2008 - Zootaxa 1686: 1-28
    The 'Celestial Pearl danio' is a miniature Danio (s.s) (Ostariophysi: Cyprinidae): evidence from morphology and molecules.
  2. Fang, F., 2003 - Copeia 2003(4): 714-728
    Phylogenetic Analysis of the Asian Cyprinid Genus Danio (Teleostei, Cyprinidae).
  3. Fang, F., M. Norén, T. Y. Liao, M. Källersjö and S. O. Kullander, 2009 - Zoologica Scripta 38(1): 1-20
    Molecular phylogenetic interrelationships of the south Asian cyprinid genera Danio, Devario and Microrasbora (Teleostei, Cyprinidae, Danioninae).
  4. Kottelat, M., 2013 - The Raffles Bulletin of Zoology Supplement 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. Mayden, R. L., K. L. Tang, K. W. Conway, J. Freyhof, S. Chamberlain, M. Haskins, L. Schneider, M. Sudkamp, R. M. Wood, M. Agnew, A. Bufalino, Z. Sulaiman, M. Miya, K. Saitoh, S. He, 2007 - Journal of Experimental Zoology, Molecular Development and Evolution 308B: 642–654
    Phylogenetic relationships of Danio within the order Cypriniformes: a framework for comparative and evolutionary studies of a model species.
  6. Roberts, T. R., 2007 - Raffles Bulletin of Zoology 55(1): 131-140
    The 'Celestial Pearl Danio', a new genus and species of colourful minute cyprinid fish from Myanmar (Pisces: Cypriniformes).

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