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Brachyplatystoma tigrinum

Zebra Shovelnose

Britski, 1981

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Subadult individual; origin unspecified.
Subadult individual; origin unspecified.Enrico Richter

Quick facts

Length
500mm SL20in SL
Tank base
1000 × 400cm394 × 157in
Temp
22–32°C72–90°F
pH
6.0–7.6
Hardness
1–12dGH

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

This species is sometimes confused with B. juruense, especially when juvenile, but can be told apart quite easily by it's more well-defined colour pattern, relatively slender body shape and longer barbels. It was described in the genus Meredontotus, but is currently included in Brachyplatystoma based on a pair of synapomorphies shared by memb...

Distribution

Upper Amazon basin. Type locality is the falls of Cachoeira do Teotônio, situated on the rio Madeira in Rondônia state, northwestern Brazil, a whitewater cataract through which water flows at an enormous volume and rate.

It's also been recorded in the Caquetá, and Putomayo basins in Colombia, plus the Ucayali and Marañon watersheds in Peru. The majority of those seen in the aquarium trade are apparently captured around the city of Iquitos in Loreto Region of the latter.

Habitat

Inhabits main river channels containing white-coloured water with a high proportion of dissolved solids, low transparency, high dissolved oxygen (around 5 mg/l), and neutral pH. Water flow is typically strong, and adults are often associated with cataracts and stretches of rapids.

While adults appear to be obligate inhabitants of main river channels, juveniles measuring 20 – 50 mm0.8 – 2.0 in are frequently collected for the aquarium trade from small tributary drainages around Iquitos in Peru, especially in areas where rice is cultivated when water levels are low. These are frequently grown on to a size of 150 – 180 mm6 – 7 in in commercial or artisanal facilities in order to obtain a better price from ornamental fish exporters.

Aquarium size

Standard length
500mm SL20in SL
Aquarium base
1000 × 400cm394 × 157in
Volume
~160000litres~42268US gal

Base dimensions of 1000 ∗ 400 cm394 ∗ 157 in or equivalent are required for long-term care.

Maintenance

The choice of décor is as much down to personal preference as anything else though a carefully-aquascaped, planted set-up is obviously out of the question.

A sandy substrate with some large chunks of driftwood, or a completely bare arrangement are perhaps the most-favoured options in privately-owned aquaria, but provided water quality is maintained and lighting not too bright this species is relatively unfussy.

An enormous, reliable filter system, rigorous maintenance regime comprising weekly water changes of 50-70% tank volume, and provision of highly-oxygenated water with plenty of movement should be considered mandatory.

Water conditions

Temperature
22–32°C72–90°F
pH
6.0–7.6
Hardness
1–12dGH

Diet

Almost entirely piscivorous preying on smaller fishes captured in the water column in nature, though most specimens readily adapt to dead alternatives such as prawn/shrimp, mussel, squid, whitebait, strips of larger white fish, etc., in aquaria. Adults require just a single meal per week at most.

Behaviour and compatibility

Only keep with species large enough to avoid predation and that require similar environmental conditions.

Sexual dimorphism

Unknown.

Reproduction

Unrecorded in captivity. In nature spawning is known to commence at the end of the dry season with early growth occurring between June and November. Unlike some members of the genus this species does not appear to undergo pan-Amazonian migrations as part of its life cycle.

Notes

This species is sometimes confused with B. juruense, especially when juvenile, but can be told apart quite easily by it's more well-defined colour pattern, relatively slender body shape and longer barbels. It was described in the genus Meredontotus, but is currently included in Brachyplatystoma based on a pair of synapomorphies shared by members (see below).

It can be distinguished from all congeners by the following external characters: colour pattern in adults comprising narrow dark vertical, oblique or scroll-like bars, rarely broken into spots; base body colour pale cream, caudal-fin with vertical bars; colour pattern in juveniles comprising a mid-lateral row of spots which expand to form adult pattern; caudal-fin in adults moderately-forked with broad, more-or-less evenly-sized lobes, filaments present in adults; eye diameter fits more than 10 times in length of snout; maxillary barbels in adults reaching dorsal-fin base, often to origin of adipose-fin; caudal peduncle compressed with greater depth than width; origin of adipose-fi anterior to origin of anal-fin; base length of adipos-fin approximately 1.3 times that of anal-fin; height of adipose-fin approximately three times its length; opercle triangular; 18 anal-fin rays.

Brachyplatystoma spp. are distinguished from all other catfishes by two synapomorphies. The first comprises several morphological characters relating to the skull, specifically that the mandibular suspensorium (that which connects the lower jaw bone to the skull) is greatly expanded mediodorsally to form a large plate approaching the parasphenoid bone, with the hyomandibula and metapterygoid similarly enlarged.

The second is the presence of an elongate filament formed from a single, unbranched simple ray on both caudal fin lobes in juveniles and subadults. These become shorter or are lost in adult specimens of B. vaillantii, B. filamentosum, B. rousseauxii, and B. capapretum but retained in B. juruense, B. platynemum and B. tigrinum.

References

  1. Ferraris, C. J., Jr. (2007). Checklist of catfishes, recent and fossil (Osteichthyes: Siluriformes), and catalogue of siluriform primary types. Zootaxa 1418, 1-628
  2. Lundberg, J. G. and A. Akama (2005). Brachyplatystoma capapretum: a new species of goliath catfish from the Amazon basin, with a reclassification of allied catfishes. Copeia 2005(3), 492-516
  3. M. Petrere Jr., R. B. Barthem, E. A. Córdoba and B. Corrales Gómez (2004). Review of the large catfish fisheries in the upper Amazon and the stock depletion of piraíba (Brachyplatystoma filamentosum Lichtenstein). Reviews in Fish Biology and Fisheries 14, 403-414
  4. Alcántara, F., F. Chu, L. Rodriguez, C. Chávez, A. Bernuy, T. Barbarán, S. Tello, G. Murrieta, C. García-Dávila, and J. Nuñez (2009). Notas sobre la Biología y Pesca del Zúngaro Tigrinis Brachyplatystoma tigrinum (Britski, 1981) en el Río Amazonas, Perú. Folia Amazonica 18(1-2), 15-22
  5. Alcántara, F., F. Chu-Koo, L. Rodríguez, C. Chávez, S. Tello, A. García, G. Murrieta, J. Mori, J. Nuñez, C. García-Dávila, and F. Duponchelle (2009). Plan de Manejo del Zúngaro Tigrinus Brachyplatystoma tigrinum en la Amazonía Peruana. Folia Amazonica 18(1-2), 59-66

Distribution

Profile completeness21 of 24

88% complete

Missing: temperament, water condition notes, etymology.