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Hypsolebias sertanejo

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        Rivulidae
    • - Classification -
    • Cynolebiinae
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Hypsolebias sertanejo Costa, 2012

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drawing shows typical species in Rivulidae.

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

Teleostei (teleosts) > Cyprinodontiformes (Rivulines, killifishes and live bearers) > Rivulidae (Rivulines) > Cynolebiinae
Etymology: sertanejo: The name sertanejo is a Portuguese word which means something or someone originating in the Sertão, which is a general term designating a vast area of the savannahs of central and north-eastern Brazil, derived from the Portuguese word ‘desertão’ (big desert), in reference to the scarce human occupation of the region in the past, associated with the warm and dry climate. This species occurs in the area that is part of the region described in the famous novel Grande Sertão.

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

Freshwater; benthopelagic. Tropical

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

South America: São Francisco River basin, Brazil.

Size / Weight / Age

Maturity: Lm ?  range ? - ? cm
Max length : 4.8 cm SL male/unsexed; (Ref. 89836); 3.9 cm SL (female)

Short description Identification keys | Morphology | Morphometrics

Dorsal soft rays (total): 18 - 25; Anal soft rays: 18 - 23; Vertebrae: 28 - 30. Distinguished from all members of the Hypsolebias flavicaudatus complex, except H. janaubensis and H. nitens, by having elongated bluish white spots on the posterior portion of the dorsal-fin base in males (vs. spots not elongated). Differs from H. nitens by having grey bars of flank in males slightly narrower, equal or slightly wider than the interspace (vs. about two or three times wider), black spots on the middle of the flank in females larger than pupil (vs. smaller), and dorsal and anal fin filaments in males long, reaching the posterior third of the caudal fin (vs. short, reaching the anterior half of the caudal fin), and from H. janaubensis by having longer dorsal-fin base in males (38.7-43.5% SL vs. 34.4-38.4% SL), and deeper body and caudal peduncle (body depth 39.7-43.2 SL% in males and 37.2-40.8% SL in females vs. 33.9-39.5% SL and 30.7-36.8% SL, respectively; caudal peduncle depth 14.8-16.1% SL in males and 14.4-15.4% SL in females vs. 12.6-14.7% SL and 11.7-13.6% SL, respectively). Also differs from H. flavicaudatus and H. gilbertobrasili by having more grey bars on the flank in males (11-15 vs. 8-10); from H. flavicaudatus, H. gilbertobrasili and H. guanambi by the presence of short bluish white bars on the anterior portion of the dorsal-fin base in males (vs. absence); from H. radiseriatus and H. pterophylus by having shorter dorsal and anal fin filaments (reaching posterior portion of caudal fin, sometimes barely surpassing posterior caudal-fin margin vs. in much surpassing posterior caudal-fin margin) and fewer dorsal fin filaments (2-3 vs. 4-6); from H. flavicaudatus by narrower head in males (64.1-68.8% of head length vs. 70.4-73.1%); from H. flagellatus, H. radiseriatus and H. gilbertobrasili by smaller black spot on the middle of the flank in females (smaller than eye vs. approximately equal to eye in H. flagellatus and H. radiseriatus, and greater than eye in H. gilbertobrasili). Differs also from other species of the the H. flavicaudatus complex by the rudimentary contact organs often present on the anteroventral part of the flank in males (Ref. 89836).

Biology     Glossary (e.g. epibenthic)

Occurs in parts of the seasonal pools more exposed to sunlight, but often with dense aquatic vegetation (Ref. 89836).

Life cycle and mating behavior Maturity | Reproduction | Spawning | Eggs | Fecundity | Larvae

Main reference Upload your references | References | Coordinator : Costa, Wilson J.E.M. | Collaborators

Costa, W.J.E.M., P.F. Amorim and J.L. Mattos, 2012. Species delimitation in annual killifishes from the Brazilian Caatinga, the Hypsolebias flavicaudatus complex (Cypriniformes: Rivulidae): implications for taxonomy and conservation. Systematics and Biodiversity 10(1):71-91. (Ref. 89836)

IUCN Red List Status (Ref. 130435: Version 2024-2)

  Least Concern (LC) ; Date assessed: 07 November 2018

CITES

Not Evaluated

CMS (Ref. 116361)

Not Evaluated

Threat to humans

  Harmless





Human uses

FAO - Publication: search | FishSource |

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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 = 0.5000   [Uniqueness, from 0.5 = low to 2.0 = high].
Bayesian length-weight: a=0.01995 (0.00906 - 0.04395), b=3.01 (2.83 - 3.19), in cm total length, based on all LWR estimates for this body shape (Ref. 93245).
Trophic level (Ref. 69278):  3.2   ±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).


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