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Colomesus psittacus

Banded Puffer

Bloch & Schneider, 1801

Formerly Tetrodon psittacus Bloch & Schneider, 1801 · Tetrodon semispinosus Fréminville, 1813

On this page13 sections
Specimen from coastal Brazil.
Specimen from coastal Brazil.Hans Hillewaert/Tomas Willems

Quick facts

Length
290mm SL11in SL
Tank base
180 × 60cm72 × 24in
Temp
20–26°C68–79°F
pH
7.0–9.0
Hardness
10–25dGH

Difficulty5 of 6 measures

Moderate

More bars, more demanding.

Space
very large tank
Water
tap water
Temp
unfussy
Temperament
unknown
Social
kept alone
Compatibility
not a community fish

Although it does penetrate the lower basins of rivers, particularly the Amazon where it has been collected from the rio Xingu several hundred kilometres from its mouth, this species is predominantly an inhabitant of mangrove swamps, estuaries, and other such saline habitats. It is particularly common in tidal channels, shallow inshore lagoons, and the lower reaches of rivers.

Etymology

Colomesus: from the Ancient Greek χωλóς (cholós), meaning 'physically defective, crippled', and μέσος (mésos), meaning 'middle', presumably in reference to the frontal bones being narrowed, not connected to the orbit, and with the elongated postfrontals connected to the prefrontals (see Gill 1884, also note misspelling of χωλóς as Κολoς).

psittacus: from the Ancient Greek ψιττακός (psittakós), meaning 'parrot', persumably in reference to this species' beak-like mouthparts.

Distribution

This species' known range extends eastwards from the Parque Nacional Natural Tayrona in Magdalena Department, Colombia, across northern Venezuela, the Gulf of Paria and Orinoco Delta, then southwards via the Guyanas and past the mouth of the Amazon, with the southernmost records from Sergipe state in northeastern Brazil. It is also known from Trinidad and Tobago and Caribbean islands including the Greater Antilles, Lesser Antilles, and Bahamas.

Records from the middle and upper Amazon basins appear to represent misidentifications of the congener C. asellus.

Type locality is given in error as 'Indian Ocean'.

Habitat

Although it does penetrate the lower basins of rivers, particularly the Amazon where it has been collected from the rio Xingu several hundred kilometres from its mouth, this species is predominantly an inhabitant of mangrove swamps, estuaries, and other such saline habitats.

It is particularly common in tidal channels, shallow inshore lagoons, and the lower reaches of rivers.

Aquarium size

Standard length
290mm SL11in SL
Aquarium base
180 × 60cm72 × 24in
Volume
~648litres~171US gal

An aquarium measuring 180 ∗ 60 ∗ 60 cm72 ∗ 24 ∗ 24 in is suggested as a bare minimum, but even this may prove too small for long-term care.

Maintenance

Choice of décor is not especially critical though it should be maintained in a well-decorated set-up, perhaps containing some driftwood roots or branches in order to mimic its natural mangrove habitats.

It is intolerant of organic waste and require spotless water in order to thrive. Moderate levels of dissolved oxygen and water movement are also recommended, meaning additional powerheads, pumps, etc., should be employed as necessary. A linear flow pump may prove a useful addition, while weekly water changes of 30-50% should be considered mandatory.

Wild examples can be delicate and sensitive to white spot/ich post-import, so a lengthy quarantine period may be required. Maintenance in pure freshwater may also present problems, so the addition of marine salt to a standard gravity of ≥1.010 is recommended.

Water conditions

Temperature
20–26°C68–79°F
pH
7.0–9.0
Hardness
10–25dGH

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Diet

Chiefly carnivorous and feeds almost exclusively on molluscs and crustaceans such as Cirripedia (barnacles) and Brachyuran crabs, taking increasingly mobile prey as it matures. There is also evidence to suggest seasonal changes in diet, with crabs favoured during drier periods.

In the aquarium offer unshelled crab legs, cockles, mussels, prawns, etc. Tetraodontids lack true teeth, the jawbone itself being modified into four fused toothlike structures. These grow continuously at a surprising rate, so such a diet is essential in order to maintain them at a reasonable length.

Behaviour and compatibility

Juveniles apparently form loose aggregations in the wild, but in the confines of an aquarium this species is likely to prove aggressive in all but the largest systems.

Sexual dimorphism

Unknown.

Reproduction

Unrecorded.

Notes

This species is also referred to as 'parrot puffer' in the ornamental trade, although it is not a popular aquarium fish.

Within the genus Colomesus, it can be immediately identified from congeners by its larger adult size, possession of 17-19 (vs. 13-16) pectoral-fin rays, presence of 6 (vs. 5) transverse dark bands dorsally on the body, and predominantly brackish, coastal (vs. freshwater, fluvial) ecology.

Tetraodontids are commonly referred to as 'puffers' due to the ability of many species to inflate their body to an enormous size when stressed or threatened. This is achieved by drawing water into a specialised ventral diverticulum of the stomach, although air can also be used if the fish is removed from the water. As a result of these morphological adaptations puffers swim via a unique combination of pectoral and median fin undulations referred to as 'diodontiform' swimming. They are also able to produce sounds by grinding the jaw/pharyngeal teeth or vibrating the swim bladder. Puffers are secondary freshwater fishes, with the majority of members exclusively inhabiting marine environments.

Other defining characters of tetraodontids include a tough skin usually covered with small spines, a beak-like dental plate divided by a median suture, a reduced gill opening anterior to the pectoral-fin base, no pelvic fins or spinous fin rays, typically short-based dorsal and anal fins, and no ribs.

Puffer flesh is toxic and can cause clinical poisoning and human mortality, although it is regarded as a delicacy in certain countries. The predominant toxin, usually either tetrodotoxin or saxitoxin, is dependant on species, geographic area, and time of year. The toxins are not produced by the fishes themselves, but by bacteria living in symbiotic association, or they are acquired via the food chain. Colomesus species accumulate saxitoxin, although it is unclear whether eating their flesh represents a danger to humans.

References

  1. Bloch, M. E. and J. G. Schneider (1801). M. E. Blochii, Systema Ichthyologiae Iconibus cx Ilustratum. Post obitum auctoris opus inchoatum absolvit, correxit, interpolavit Jo. Gottlob Schneider, Saxo. Berolini. Sumtibus Auctoris Impressum et Bibliopolio Sanderiano Commissum, i-lx + 1-584, Pls. 1-110
  2. Gill, T. N. (1884). Synopsis of the plectognath fishes. Proceedings of the United States National Museum 7(26-27), 411-427
  3. Amaral, C. R. L., P. M. Brito, D. A. Silva and E. F. Carvalho (2013). A new cryptic species of South American freshwater pufferfish of the genus Colomesus (Tetraodontidae), based on both morphology and DNA data. PLoS ONE 8(9), 1-15
  4. Reis, R. E., S. O. Kullander and C. J. Ferraris, Jr. (eds) (2003). Check list of the freshwater fishes of South and Central America. CLOFFSCA. EDIPUCRS, Porto Alegre, i-xi + 1-729
  5. Nelson, J. S. (2006). Fishes of the World. 4th edition. John Wiley & Sons, Hoboken, N. J., i-xix + 1-601
  6. Helfman, G., B. B. Collette, D. E. Facey, and B. W. Bowen (2009). The Diversity of Fishes: Biology, Evolution, and Ecology, 2nd Edition. Wiley-Blackwell, 1-736
  7. Tyler, J. C. (1964). A diagnosis of the two species of South American puffer fishes (Tetraodontidae, Plectognathi) of the genus Colomesus. Proceedings of the Academy of Natural Sciences of Philadelphia 116, 119-148
  8. Krumme, U., H. Keuthen, U. Saint-Paul, and W. Villwock (2007). Contribution to the feeding ecology of the banded puffer fish Colomesus psittacus (Tetraodontidae) in north Brazilian mangrove creeks. Brazilian Journal of Biology 67(3), 383-392
  9. Camargo, M., T. Giarrizzo, and V. Isaac (2004). Review of the geographic distribution of fish fauna of the Xingu river basin, Brazil. Ecotropica 10, 123-147
  10. Phillip, D. A. T., D. C. Taphorn, E. Holm, J. F. Gilliam, B. A. Lamphere and H. López-Fernández (2013). Annotated list and key to the stream fishes of Trinidad & Tobago. Zootaxa 3711(1), 1-64

One photograph on file. More would be welcome.

Distribution

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Missing: temperament, water condition notes.