You can sponsor this page

Hasemania uberaba Serra & Langeani, 2015

Upload your photos and videos
Google image
Image of Hasemania uberaba
No image available for this species;
drawing shows typical species in Characidae.

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

Teleostei (teleosts) > Characiformes (Characins) > Characidae (Characins; tetras) > Stethaprioninae
Etymology: Hasemania: Because of John D. Haseman, the American collector of fishes (Ref. 45335);  uberaba: Named for rio Uberaba, where the species is found. A noun in apposition..

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

Freshwater; benthopelagic. Tropical

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

South America: Rio Uberaba, rio Grande basin, upper rio Paraná basin in Brazil.

Size / Weight / Age

Maturity: Lm ?  range ? - ? cm
Max length : 7.0 cm SL male/unsexed; (Ref. 104709)

Short description Identification keys | Morphology | Morphometrics

Dorsal soft rays (total): 9 - 10; Vertebrae: 34 - 35. Hasemania uberaba can be distinguished from congeners by the possession of the following characsters: a black, vertically-elongate humeral spot (vs. spot absent except for H. crenuchoides, H. kalunga, H. nambiquara, and H. piatan); a single ossification in the position primitively occupied by infraorbitals four and five (vs. infraorbitals four and five separate, except in H. kalunga and H. piatan); 4 inner row premaxillary teeth (vs. 5 except in H. nana, H. melanura, and H. piatan); and scales covering the anal-fin base (vs. scales absent except in H. crenuchoides, H. hanseni, H. maxillaris, H. melanura, H. nambiquara and H. nana). It differs also from H. kalunga and H. piatan by having 14-18 circumpeduncular scales (vs. 10-12); from H. hanseni, H. maxillaris, and H. nambiquara by having 10-15 branched anal-fin rays (vs. 16-19); from H. hanseni, H. melanura, and H. nana by having 6-10 scales covering the anal-fin base (vs. 2-5); and from H. maxillaris and H. nambiquara by having 7-8 branched dorsal-fin rays (vs. 9). In addition, H. uberaba can be further diagnosed from H. melanura by having maxillary teeth (vs. absent); from H. maxillaris by having, 6-7 branched pelvicfin rays (vs. 5); from H. nambiquara by lacking a broad black band in the midlateral line from the humeral region to the caudal-fin (vs. presence of such band). Most specimens of H. uberaba possess 18 principal caudal-fin rays (vs. 19 in most other species except H. piatan) (Ref. 104709).

Biology     Glossary (e.g. epibenthic)

Known only from its type locality in the headwaters of the rio Uberaba. These headwaters are marshlands with abundant Cyperaceae, Poaceae and algae, crystalline water and muddy bottom. Collected together with a new genus and new species of Crenuchidae, the most abundant species (under analysis), Hyphessobrycon uaiso and Rivulus sp. Feeds on angiosperms, Chironomidae larvae (Diptera) and Trichopterans (Ref. 104909).

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

Main reference Upload your references | References | Coordinator | Collaborators

Serra, J.P. and F. Langeani, 2015. A new Hasemania Ellis from the upper rio Paraná basin, with the redescription of Hasemania crenuchoides Zarske & Géry (Characiformes: Characidae). Neotrop. Ichthyol. 13(3):479-486. (Ref. 104709)

IUCN Red List Status (Ref. 130435)

  Least Concern (LC) ; Date assessed: 27 October 2020

CITES

Not Evaluated

CMS (Ref. 116361)

Not Evaluated

Threat to humans

  Harmless





Human uses

FAO - Publication: search | FishSource |

More information

Trophic ecology
Food items
Diet compositions
Food consumptions
Food rations
Predators
Ecology
Ecology
Population dynamics
Growths
Max. ages / sizes
Length-weight rel.
Length-length rel.
Length-frequencies
Mass conversions
Recruitments
Abundances
Life cycle
Reproduction
Maturities
Fecundities
Spawnings
Spawning aggregations
Egg(s)
Egg developments
Larvae
Larval dynamics
Distribution
Countries
FAO areas
Ecosystems
Occurrences
Introductions
BRUVS - Videos
Anatomy
Gill areas
Brains
Otoliths
Physiology
Body compositions
Nutrients
Oxygen consumptions
Swimming type
Swimming speeds
Visual pigment(s)
Fish sounds
Diseases / Parasites
Toxicities (LC50s)
Genetics
Genetics
Electrophoreses
Heritabilities
Human related
Aquaculture systems
Aquaculture profiles
Strains
Ciguatera cases
Stamps, coins, misc.
Outreach
Collaborators
Taxonomy
Common names
Synonyms
Morphology
Morphometrics
Pictures
References
References

Tools

Special reports

Download XML

Internet sources

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 = 0.5020   [Uniqueness, from 0.5 = low to 2.0 = high].
Bayesian length-weight: a=0.01202 (0.00548 - 0.02637), b=3.08 (2.90 - 3.26), 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
Resilience (Ref. 120179):  High, minimum population doubling time less than 15 months (Preliminary K or Fecundity.).
Fishing Vulnerability (Ref. 59153):  Low vulnerability (10 of 100).