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Annamia cf. thuathienensis

Nguyen, 2005

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These specimens were exported into Germany by Saigon Aquarium Corp. in early 2010.
These specimens were exported into Germany by Saigon Aquarium Corp. in early 2010.Thomas Frank

Quick facts

Length
100mm SL3.9in SL
Tank base
120 × 30cm48 × 12in
Temp
16–22°C61–72°F
pH
6.0–7.5
Hardness
1–10dGH

Difficulty6 of 6 measures

Moderate

More bars, more demanding.

Space
large tank
Water
tap water
Temp
steady heat
Temperament
peaceful
Social
shoal
Compatibility
not a community fish

Annamia spp. may be confused with related genera such as those of the genus Balitoropsis. They can be identified by their more depressed body shape, elongate lower caudal-fin lobe, and the presence of a single unbranched ray in the pectoral and pelvic fins. At least one undescribed member of the genus is thought to exist.

Etymology

Annamia: named for Annam, a former French protectorate which today comprises the central region of Vietnam.

thuathienensis: named for Thua Thiên Province, Vietnam, where this species was discovered, in combination with the Latin suffix -ensis, meaning 'of or from a place'.

Distribution

Described from the Bô River, Thua Thien-Hue Province, central Vietnam. At present, there are no additional records.

Habitat

Largely unconfirmed, but its ecology should be similar to that of A. normani which inhabits shallow, swiftly-flowing stretches of streams and small rivers.

These are characterised by crystal clear water, and these loaches tend to be restricted to riffles, rapids, and swiftly-flowing runs with rocky substrates.

In one study adults were found to live in rapids, feeding selectively on cyanobacteria (see 'Diet'), whereas juveniles occupied shallower water grazing organic detritus.

Aquarium size

Standard length
100mm SL3.9in SL
Aquarium base
120 × 30cm48 × 12in
Volume
~108litres~29US gal

Minimum base dimensions of 120 ∗ 30 cm48 ∗ 12 in or equivalent are required.

Maintenance

Since Annamia spp. are obligate residents of riffles and rapids in nature it is essential to maintain them in a set-up designed to resemble such a habitat.

Use a substrate of gravel, sand (or a mixture), and add a layer of variably-sized water-worn rocks and boulders plus some driftwood roots or branches if you wish. While the majority of aquatic plants will fail to thrive in such surroundings, hardy genera such as Microsorum, Bolbitis, or Anubias can usually be grown attached to the décor, while bright lighting will promote the growth of aufwuchs upon which the fish will graze.

Like many species that naturally inhabit running waters they are intolerant to the accumulation of organic waste, and requires spotless water in order to thrive. High levels of dissolved oxygen and water movement are also essential with a recommended turnover of 10-15 times per hour, meaning additional powerheads, airstones, etc., should be employed as necessary.

Since stable water conditions and the presence of biofilm are obligatory for their well-being these fish should never be added to biologically-immature aquaria, and weekly water changes of 30-50 % aquarium volume should be considered mandatory.

Water conditions

Temperature
16–22°C61–72°F
pH
6.0–7.5
Hardness
1–10dGH

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Diet

Traditionally considered to be a micropredator feeding on insect larvae and suchlike (Rainboth, 1996)[3], but a study by Herder and Freyhof (2006)[1] revealed adult A. normani inhabiting the Duc My River in central Vietnam to be specialised grazers of cyanobacteria. In rapids the latter form hard encrustations on rock surfaces from which adults are able to bite chunks.

Whether this behaviour is only representative of A. normani, or even restricted to particular populations, is unclear but it would seem wise to offer dried foods containing Spirulina or similar alongside chironomid larvae (bloodworm), Tubifex, Artemia, etc., and ideally allow aufwuchs to grow on all surfaces in the tank except the viewing pane.

Gastromyzontids are often seen on sale in an emaciated state which can be difficult to correct. A good dealer will have done something about this, but if you decide to take a chance with specimens in which the body appears narrowed, especially between the pectoral and pelvic fins, they will need a constant supply of suitable foods and should be kept alone until strong enough to compete with other species.

Behaviour and compatibility

Largely peaceful, although its environmental requirements limit the choice of suitable tankmates somewhat. Species inhabiting similar environments include Barilius, Opsarius, Discherodontus, Garra, larger Devario, some Rasbora, Rhinogobius, Sicyopterus and Stiphodon gobies, plus catfishes from genera such as Glyptothorax, Akysis, and Oreoglanis.

Many loaches from the families Nemacheilidae, Balitoridae, and Gastromyzontidae are also suitable, although squabbles may occur with the latter group in particular.

Annamia are found living in large aggregations in nature so a group of eight or more should be considered the minimum purchase. When kept singly or in smaller numbers they tend to be quite shy.

Sexual dimorphism

Sexually mature females are likely to be a little larger and fuller-bodied than males.

Reproduction

Presumably a seasonal spawner in nature but has not been bred in captivity.

Notes

This species' description was published in the Vietnamese language, and very little is known about it. Some major resources fail to list it as valid, and it is considered a 'species inquirenda' by Kottelat (2012).

Annamia spp. may be confused with related genera such as those of the genus Balitoropsis. They can be identified by their more depressed body shape, elongate lower caudal-fin lobe, and the presence of a single unbranched ray in the pectoral and pelvic fins. At least one undescribed member of the genus is thought to exist.

The family Gastromyzontidae is currently considered valid following Kottelat (2012).

It contains a number of genera which had formerly been included in several families and subfamilies, most recently Balitoridae, of which the most well-known in the aquarium hobby include Beaufortia, Formosania, Gastromyzon, Pseudogastromyzon, Hypergastromyzon, Liniparhomaloptera, Sewellia and Vanmanenia.

References

  1. Herder, F. and J. Freyhof (2006). Resource partitioning in a tropical stream fish assemblage. Journal of Fish Biology 69(2), 571-589
  2. Kottelat, M. (2001). Fishes of Laos. WHT Publications, Colombo, 1-198
  3. Rainboth, W. J. (1996). Fishes of the Cambodian Mekong. FAO Species Identification Field Guide for Fishery Purposes. FAO, Rome, 1-265
  4. Šlechtová, V., J. Bohlen and H. H. Tan (2007). Families of Cobitoidea (Teleostei; Cypriniformes) as revealed from nuclear genetic data and the position of the mysterious genera Barbucca, Psilorhynchus, Serpenticobitis and Vaillantella. Molecular Phylogenetics and Evolution 44(3), 1358-1365
  5. Tang, Q., H. Liu, R. Mayden and B. Xiong (2006). Comparison of evolutionary rates in the mitochondrial DNA cytochrome b gene and control region and their implications for phylogeny of the Cobitoidea (Teleostei: Cypriniformes). Molecular Phylogenetics and Evolution 39(2), 347-357
  6. Kottelat, M. (2012). Conspectus cobitidum: an inventory of the loaches of the world (Teleostei: Cypriniformes: Cobitoidei). Raffles Bulletin of Zoology Supplement 26, 1-199
  7. Randall, Z. S. and L. M. Page (2012). Resurrection of the genus Homalopteroides (Teleostei: Balitoridae) with a redescription of H. modestus (Vinciguerra 1890). Zootaxa 3586, 329-346
  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
  9. Nguyen, V. H. (2005). Cá nuóc ngot Viêt Nam. Tâp II. [Freshwater fishes of Vietnam. Volume 2]. Nhà Xuât Ban Nông Nghiêp [Agriculture Publishing House], Hanoi, 1-759

Distribution

Profile completeness22 of 24

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Missing: a common name, water condition notes.