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Ageneiosus ucayalensis

Duck Catfish

Castelnau, 1855Formerly Ageniosus porphyreus Cope, 1867

Last revised 2026Edit this page

On this page13 sections
Subadult specimen from the Río Itaya, Peru.
Subadult specimen from the Río Itaya, Peru.Erlend D. Bertelsen

Quick factsEdit

Max size
290mm SL11in SL
Aquarium size
180 × 60cm72 × 24in
Temp
22.5–28°C73–82°F
pH
5.5–7.5
Hardness
1–20dGH

Difficulty3 of 8 measures

Moderate

How the rating is worked out

Space
very large tank
Water
flexible
Temp
flexible
Diet
unknown
Temperament
unknown
Social
unknown
Compatibility
unknown

Other demands

Each of these can raise the rating on its own, whatever the measures above say.

Hardiness
unknown
  • Needs a very large tank

The duck catfish, Ageneiosus ucayalensis, is an auchenipterid catfish described from Peru and recorded across the Amazon, Orinoco and Guianas. Body patterning apparently varies with locality, and fish from black water habitats, particularly on the Guiana Shield, tend to be darker. Growing to around 290 mm SL and capable of taking large prey, it is safe only with similarly sized catfishes or large pelagic characins, mostly a combination for public aquaria.

Etymology

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Ageneiosus: from the Greek á- (Gr. ἄ), meaning 'not, without' and géneion (Gr. γένειον), meaning 'chin, beard', probably in reference to the very short maxillary barbels possessed by A. armatus (now a synonym of A. inermis).

ucayalensis: named for its type locality comprising a lake close to the Ucayali River, Peru, plus the Latin suffix -ensis, meaning 'pertaining to, originating in'.

Distribution

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Described from the Río Ucayali in Peru but subsequently recorded across a large geographic area. Records currently exist from Ecuador, Colombia, Peru, Brazil, Venezuela, Guyana and Suriname, and encompass the majority of the rio Amazon drainage plus its tributaries, the Orinoco system, Atlantic river basins of the Guianas and the Río Paraná.

Given its enormous natural range this species is likely to be something of a habitat generalist, but most records we've seen pertain to middle and lower sections of river channels and larger tributaries.

Aquarium size

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

Minimum base dimensions of 180 ∗ 60 cm72 ∗ 24 in are required for long-term care since this is an active species that can sometimes act skittishly and easily acquire injuries by swimming into the glass.

Maintenance

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Likely to prefer dim lighting and access to refuges in the form of driftwood, large rocks or lengths of plastic piping. An enormous filtration system and dedicated regime of water changes will also be required and maintenance of high dissolved oxygen levels should be considered mandatory given the species' natural habitat plus the fact that unlike some relatives it cannot respire atmospheric oxygen.

Water conditions

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Temperature
22.5–28°C73–82°F
pH
5.5–7.5
Hardness
1–20dGH

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Larger Ageneiosus spp. are obligate carnivores by nature feeding on invertebrates and other fishes, and capable of consuming surprisingly large prey. Newly-imported specimens thus often refuse to accept anything but live fishes though most can be weaned onto thawed frozen whitebait, shellfish or similar once they recognise them as edible. Some individuals even learn to accept dried foods such as pellets designed for carnivorous species.

Like the vast majority of predatory fishes this species should not be fed mammalian/avian meat such as beef heart or chicken, and similarly there is little 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 compatibility

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This species is capable of consuming large prey items and is likely to be safe only alongside similarly-sized catfishes or pelagic characins such as Brycon, Colossoma or Piaractus, a combination only possible in public aquaria in the vast majority of cases.

Sexual dimorphism

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Adult males of Ageneiosus spp. all display marked, seasonal, sexual modifications, with the area between head and dorsal fin origin (nuchal region) exhibiting a much more acute angle than in non-breeding individuals. The maxillary barbel also becomes ossified and extended inbreeding males with tooth-like odontotes apparent on the dorsal and medial surfaces, while the first branched dorsal fin ray is significantly extended giving the fin an enlarged, curved appearance with sharp odontotes appearing along the anterior margin.

The anterior portion of the anal fin in sexually-active males also exhibits seasonal modifications with the unbranched and first few branched rays becoming thickened, elongate and fused together, forming a structural support for the intromittent organ which itself becomes displaced in such a way that the genital pore is situated at the tip of the modified rays. The interradial membranes and surrounding inclinator/erector muscles also become enlarged. In adult females, the unbranched and first few branched anal-fin rays are much longer than the other rays.

Reproduction

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Unrecorded in aquaria although some brief reports of apparent courtship behaviour in the congener A. marmoratus do exist. What is known is that fertilisation occurs internally via the modified genital papillae in males described above, with the ossified and extended maxillary barbels and dorsal fin ray used to court and physically manipulate females.

Since a seasonal spawning strategy is adopted in nature, induced by the onset of the rainy season, simulation of such via a period of warmth followed by several large, cool water changes may prove useful in captivity. This species is known to perform annual migrations alongside other fishes such as Semiprochilodus spp..

Notes

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Apparently this species is polymorphic with body patterning varying significantly depending on locality. Individuals collected from black water habitats tend to be noticeably darker in overall colouration, for example, with this being particularly evident among populations from the Guiana Shield.

The genus Ageneiosus was at one point classified in the family Ageneiosidae alongside the genus Tetranematichthys, but this was not accepted by all authors. The grouping remains poorly-studied with the last major revision having been conducted by Walsh (1990) in his unpublished dissertation. Following that paper A. ucayalensis can be told apart from congeners by the following combination of characters: caudal fin deeply forked; body significantly elongate and laterally compressed; head flattended with mouth markedly inferior; anal fin very long with 41-50 rays; gill rakers on first arch long with small, toothlike projections.

The genus, meanwhile, is separated from other auchenipterids by a combination of absence of mental barbels in adults, and the presence of enlarged, tooth-like odontodes formed by outgrowths of the maxillae on the dorsal margin of the maxillary barbels inbreeding males. The larger-growing members are often utilised as food fishes in their native countries.

The family Auchenipteridae is itself distinguished from all other catfishes by the following: body lacking bony plates except on dorsal surface between head and dorsal fin origin which is covered by a row of such plates joined together and clearly visible beneath a thin epidermis; no nasal barbel(s); adipose fin small, occasionally absent; eye covered by adipose tissue and lacking a distinct orbital rim; anterior anal fin rays enlarged and thickened in adult males; maxillary barbel fits in a specialised groove below the eye when drawn towards the body; maxillary barbel directed laterally and dorsally when drawn into said groove

References

  1. Castillo, G. O. and G. Oscar Brull (1989). Ageneiosus magoi una nueva especie de bagre ageneiosido (Teleostei, Siluriformes) para Venezuela y algunas notas sobre su historia natural. Acta Biologica Venezuelica 12(3-4), 72-87
  2. Ferraris, C. J., Jr. (2007). Checklist of catfishes, recent and fossil (Osteichthyes: Siluriformes), and catalogue of siluriform primary types. Zootaxa 1418, 1-628
  3. 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
  4. Ribeiro, F. R. V. and L. H. Rapp Py-Daniel (2010). Ageneiosus uranophthalmus, a new species of aucheniperid catfish (Osteichthyes: Siluriformes) from river channels of the central Amazon basin, Brazil. Neotropical Ichthyology 8(1), 97-104
  5. Schraml, E. (2004). 'Gotta Lotta Bottle'. Today's Fishkeeper, November 2004, 32-34
  6. Sullivan, J. P., J. G. Lundberg and M. Hardman (2006). A phylogenetic analysis of the major groups of catfishes (Teleostei: Siluriformes) using rag1 and rag2 nuclear gene sequences. Molecular Phylogenetics and Evolution 41(3), 636–662
  7. Walsh, S. J. (1990). A Systematic Revision of the Neotropical Catfish Family Ageneiosidae (Teleostei: Ostariophysi: Siluriformes). Unpublished Ph.D. Dissertation, University of Florida, Gainesville, 1-363