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Brachyhypopomus alberti Crampton, de Santana, Waddell & Lovejoy, 2017

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drawing shows typical species in Hypopomidae.

Classification / Names Common names | Synonyms | Catalog of Fishes(genus, species) | ITIS | CoL | WoRMS | Cloffa

Teleostei (teleosts) > Gymnotiformes (Knifefishes) > Hypopomidae (Bluntnose knifefishes)
Etymology: Brachyhypopomus: Greek, brachys, eia = short + Greek, hypo = under + Greek, poma, -atos = cover (Ref. 45335);  alberti: Named for James S. Albert, American (USA) ichthyologist, collector of part of the type series, for his enormous contributions to the systematic biology of gymnotiform fishes..

Environment: milieu / climate zone / depth range / distribution range Ecology

Freshwater; benthopelagic; pH range: 5.2 - 5.5. Tropical; 22°C - 24°C (Ref. 116763)

Distribution Countries | FAO areas | Ecosystems | Occurrences | Point map | Introductions | Faunafri

South America: upper rio Madeira basin in Brazil and Bolivia.

Size / Weight / Age

Maturity: Lm ?  range ? - ? cm
Max length : 11.1 cm TL male/unsexed; (Ref. 116763); 10.0 cm TL (female)

Short description Identification keys | Morphology | Morphometrics

Anal soft rays: 172 - 191. Brachyhypopomus alberti is distinguished from other species of the genus Brachyhypopomus by the following combination of characters: absence of depigmented stripe along middorsal region of body (vs. prominent pale uninterrupted middorsal stripe from occipital region to base of caudal filament in B. arrayae, B. beebei, B. belindae, B. gauderio, B. pinnicaudatus, and B. verdii); 20-22 precaudal vertebrae (vs. 15-19 in B. batesi, B. benjamini, B. bennetti, B. bombilla, B. bullocki, B. cunia, B. diazi, B. hendersoni, B. menezesi, B. provenzanoi, B. regani, and B. sullivani); anal fin with 182-202 rays (vs. 226-293 in B. brevirostris); presence of continuous or discontinuous dark vertical or diagonally oriented bands or saddles on body surface dorsal to lateral line, often extending across lateral line into ventral lateral surface (vs. absence of oblique bands or saddles on body surface dorsal to lateral line in B. draco, B. flavipomus, B. jureiae, and B. palenque); 3 bilateral columns of electrocytes at the anal-fin terminus (vs. 4-5 in B. janeiroensis and B. occidentalis (except some populations in Colombia and Venezuela); absence of dark suborbital stripe (vs. presence in B. walteri). It differs from most but not all specimens of B. hamiltoni by having a higher number of pectoral-fin rays 15-16 (mode 16) (vs. 12-15 (mode 13) (only 2 of 18 measured specimens of B. hamiltoni exhibited an overlapping number of pectoral-fin rays with B. alberti). It can be differentiated from B. hamiltoni by the absence of the first of five branchiostegal rays (vs. presence in B. hamiltoni Mago-Leccia) (Ref. 116763).

Biology     Glossary (e.g. epibenthic)

Facultative air-breathing in the genus (Ref. 126274); The type series was sampled in tropical forest and savanna near Riberalta, Bolivia from small low-conductivity clearwater and blackwater terra firme streams. Found mostly commonly in marginal root mats, and in emergent or submerged aquatic vegetation. Recorded water parameters at the sampling sites included the following: conductivity 5-15 μS/cm, dissolved oxygen 3.0-5.0 mg/l, temperature 22-24°C, and pH 5.2-5.5. Co-inhabits in geographical sympatry and ecological syntopy with the following species occurring in terra firme stream: B. brevirostris, B. sullivani, and B. walteri. In the region of the type locality, it is allotopic with whitewater floodplain species such as B. arrayae, B. bombilla, and B. pinnicaudatus. It co-occurs in geographical sympatry with its sister species B. arrayae, but the species exhibit a noteworthy difference in ecological distribution. B. alberti occupies the low conductivity (ca. 5-15 μScm-1) terra firme forest and savanna streams, while B. arrayae mainly inhabits higher-conductivity whitewater floodplain systems (ca. 150 μScm-1 at the time of sampling). B. alberti was collected together with B. arrayae (and also B. pinnicaudatus) in the lower reaches of terra firme streams, at the ecotone with the río Beni floodplain (Ref. 116763).

Life cycle and mating behavior Maturities | Reproduction | Spawnings | Egg(s) | Fecundities | Larvae

Main reference Upload your references | References | Coordinator : Albert, James S. | Collaborators

Crampton, W.G.R., C.D. de Santana, J.C. Waddell and N.R. Lovejoy, 2017. A taxonomic revision of the Neotropical electric fish genus Brachyhypopomus (Ostariophysi: Gymnotiformes: Hypopomidae), with descriptions of 15 new species. Neotrop. ichthyol. 14(4):e150146. (Ref. 116763)

IUCN Red List Status (Ref. 130435)


CITES

Not Evaluated

CMS (Ref. 116361)

Not Evaluated

Threat to humans

  Harmless





Human uses

FAO - Publication: search | FishSource |

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AFORO (otoliths) | Aquatic Commons | BHL | Cloffa | BOLDSystems | Websites from users | Check FishWatcher | CISTI | Catalog of Fishes: genus, species | DiscoverLife | ECOTOX | FAO - Publication: search | Faunafri | Fishipedia | Fishtrace | GenBank: genome, nucleotide | GloBI | Google Books | Google Scholar | Google | IGFA World Record | MitoFish | Otolith Atlas of Taiwan Fishes | PubMed | Reef Life Survey | Socotra Atlas | Tree of Life | Wikipedia: Go, Search | World Records Freshwater Fishing | Zoobank | Zoological Record

Estimates based on models

Phylogenetic diversity index (Ref. 82804):  PD50 = 0.5000   [Uniqueness, from 0.5 = low to 2.0 = high].
Bayesian length-weight: a=0.00380 (0.00145 - 0.00994), b=3.06 (2.83 - 3.29), in cm total length, based on LWR estimates for this (Sub)family-body shape (Ref. 93245).
Trophic level (Ref. 69278):  3.1   ±0.4 se; based on size and trophs of closest relatives
Fishing Vulnerability (Ref. 59153):  Low vulnerability (10 of 100).