Acanthodoras spinosissimus (EIGENMANN & EIGENMANN, 1888)

Chocolate Talking Catfish

Classification

Order: Siluriformes Family: Doradidae

Distribution

Described from Lago do Coari (Lake Coari) on the rio Solimões at Coari, Amazonas state, northwestern Brazil and subsequently recorded throughout much of the northern Amazon basin in Peru, Colombia and Brazil, plus the Río Essequibo drainage in Guyana.

Habitat

Slow-moving and standing waters including tributaries, backwaters, freshwater swamps and coastal mangroves where it’s typically found sheltering among roots or submerged vegetation during daylight hours before emerging at night to forage. It often occurs in large aggregations alongside other doradids such as Platydoras armatulus, Agamyxis pectinifrons, and Platydoras hancockii.

In the Iwokrama Forest, central Guyana it has been recorded to coexist with around 400 other species of which some available in the aquarium hobby include Anostomus anostomus, Hemigrammus belottii, H. ocellifer, Hyphessobrycon bentosi, H. rosaceus, Moenkhausia collettii, Pristella maxillaris, Carnegiella strigata, Hemiodus argenteus, H. gracilis, Nannostomus eques, N. marginatus, N. trifasciatus, Bunocephalus coracoideus, Callichthys callichthys, Corydoras melanistius, Megalechis thoracata, the congeneric Acanthodoras cataphractus, Ancistrus hoplogenys, Hemiodontichthys acipenserinus, Hemiloricaria fallax, Apteronotus albifrons, Eigenmannia virescens, Biotodoma cupido, Geophagus brachybranchus, Pterophyllum scalare, Satanoperca jurupari, S. leucosticta and Colomesus asellus.

Maximum Standard Length

The largest officially-recorded specimen measured 137 mm.

Aquarium SizeTop ↑

Base dimensions of at least 120 cm x 30 cm are recommended.

Maintenance

Best maintained in a dimly-lit set-up with a soft, sandy substrate and plenty of cover in the form of aquatic vegetation, tangles of driftwood or artificial caves of some kind. Bright lighting isn’t really appreciated since this species is largely nocturnal by nature.

Water Conditions

Temperature: 22 – 26 °C

pH: 6.0 – 7.5

Hardness: 72 – 447 ppm

Diet

This species is an omnivorous generalist and will accept most commonly-encountered prepared and frozen foods. A varied diet comprising good quality, dried, sinking pellets or tablets supplemented by regular meals of live or frozen bloodworm, Tubifex, mosquito larvae, etc. is ideal, and the occasional whole or chopped earthworm will provide valuable additional protein.

Behaviour and CompatibilityTop ↑

Non-aggressive though adult individuals may consume very small fishes. It makes an excellent addition to a medium-to-large-sized community of Amazonian species alongside peaceful characins, cichlids and other catfishes, for example. It’s gregarious by nature so buy at least 4 specimens, and it will also group together with similarly-looking relatives such as Platydoras armatulus, Agamyxis pectinifrons, and Amblydoras hancockii.

Sexual Dimorphism

Mature females tend to be noticeably fuller-bodied than males.

Reproduction

Very little information seems to exist but apparently the congener A. cataphractus forms pair bonds with reports suggesting that both male and female are involved in excavating a shallow pit into which the eggs are deposited, plus post-spawning brood care and defence. Incubation is supposedly 4-5 days and it’s unclear whether parental care caesews

NotesTop ↑

This species, which may also be referred to by the alternative vernacular names ‘spiny catfish’, ‘painted talking catfish’ or ‘chocolate raphael’, isn’t particularly common in the trade and most often exported only as bycatch among shipments of Platydoras armatulus. It appears very similar to A. cataphractus with the most useful external distinguishing character being the presence of pale blotches on the dorsal surface, between the dorsal and caudal fins, in A. spinosissimus versus pale lines or no markings at all in A. cataphractus. Both species are sold under the same trade names.

Members of the family Doradidae can be distinguished from all other Siluriformes by possession of a unique infranuchal scute, a dermal bone consisting of an elongate plate formed by expansion of a ligament located between the posterior nuchal plate and the rib on the sixth vertebra. This feature is associated with the lateral line canal and represents the first in a series of prominent midlateral scutes exhibited by most doradids. There are two major lineages recognised within the family, one with simple barbels and a comparatively flattened head, the other with fimbriate barbels and a relatively deep head.

Within the order Siluriformes doradids are most closely related to the family Auchenipteridae, most commonly referred to as ‘driftwood’ catfishes by aquarists, and these two were grouped together in the superfamily Doradoidea by Sullivan et al. (2006). In their molecular phylogenetic analysis Doradoidea appeared to form a sister group pairing with the family Aspredinidae (banjo catfishes) with this constituting a significant departure from earlier hypotheses in which the African family Mochokidae and Asian Sisoridae were assumed to be most closely-associated with doradids and aspredinids, respectively. The authors stopped short of naming this putative Aspredinidae-Doradoidea clade, for the time being at least, ostensibly because certain prominent theories of fish biogeography would require substantial re-assessment if it were accepted.

Doradids are often referred to collectively as ‘talking catfishes’ in reference to the fact that many of them are able to produce audible sounds. In some genera (e.g. Acanthodoras, Agamyxis) these are produced via stridulation of the pectoral spines within their sockets, with the pelvic girdle possibly involved in projection of the resultant noise. The ‘elastic-spring apparatus’ is also used to produce sound, this comprising a highly-specialised arrangement of the parapophyses of the fourth vertebrae, the swim bladder plus associated muscles and ligaments.

Take care when netting doradids for any reason since the pectoral fin spines and body scutes easily become entangled in the mesh of standard aquarium nets and can break human skin in many cases.

References

1. Birindelli, J. L. O., L. M. Sousa and M. H. Sabaj Pérez. 2008 - Neotropical Ichthyology 6(3): 465-480
   New species of thorny catfish, genus Leptodoras Boulenger (Siluriformes: Doradidae), from Tapajós and Xingu basins, Brazil.
2. Eigenmann, C. H. and R. S. Eigenmann. 1888 - Proceedings of the California Academy of Sciences (Series 2) 1(2): 119-172
   Preliminary notes on South American Nematognathi. I.
3. Moyer, G. R., B. M. Burr and C. Krajewski. 2004 - Zoological Journal of the Linnean Society 140: 551-575
   Phylogenetic relationships of thorny catfishes (Siluriformes: Doradidae) inferred from molecular and morphological data.
4. Roa-Fuentes, C. A., J. C. Alonso, A. Alfonso and M. Sabaj Pérez. 2010 - Check List, Journal of Species Lists and Distribution 6(4): 485–487
   Pisces, Siluriformes, Doradidae, Astrodoras Bleeker, 1862: First record in the Colombian Amazon
5. Sabaj, M. H. 2002 - Unpubl. DPhil thesis, University of Illinois
   Taxonomy of Doradidae (Actinopterygii: Siluriformes) with revision and phylogeny of genus Leptodoras.
6. Sabaj, M. H. and C. J. Ferraris. 2003 - In: R.E. Reis, S.O. Kullander and C.J. Ferraris, Jr. (eds.)
   Doradidae (Thorny catfishes).
7. Sullivan, J. P., J. G. Lundberg and M. Hardman. 2006 - Molecular Phylogenetics and Evolution 41: 636–662
   A phylogenetic analysis of the major groups of catWshes (Teleostei: Siluriformes) using rag1 and rag2 nuclear gene sequences.
8. Watkins, G., W. Saul, E. Holm, C. Watson, D.Arjoon and J. Bicknell. 2005 - Proceedings of the Academy of Natural Sciences of Philadelphia 154(1): 39-53
   The fish fauna of the Iwokrama Forest.