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Tatia bockmanni (Sarmento-Soares & Buckup, 2005)

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drawing shows typical species in Auchenipteridae.

klasifikasi / Names Nama-nama umum | Sinonim (persamaan) | Catalog of Fishes(Marga, Jenis) | ITIS | CoL | WoRMS | Cloffa

> Siluriformes (Catfishes) > Auchenipteridae (Driftwood catfishes) > Centromochlinae
Etymology: Tatia: Because of Mr. C. Tate Regan (Ref. 45335);  bockmanni: Named for Flávio Alicino Bockmann, Universidade de São Paulo, who collected the specimens that led us to the recognition of the species as an undescribed species (Ref. 56311).

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

; air tawar dasar (demersal); kisaran kedalaman 0 - 2 m (Ref. 56311). Tropical

Penyebaran Negara-negara | Daerah-daerah FAO | Ecosystems | Kemunculan | Point map | Introduksi | Faunafri

South America: Brazil.

Size / Weight / umur

Maturity: Lm ?  range ? - ? cm
Max length : 4.8 cm SL jantan/; (Ref. 56311)

deskripsi pendek Kunci identifiaksi (pengenalan) | Morfologi | Morfometrik

Duri punggung (Keseluruhan (total)) : 1; duri punggung lunak (Keseluruhan (total)) : 5. Diagnosis: This species is distinguished from its congeners by the autapomorphic reduced ossified suprapreopercular canal. In auchenipterids the suprapreopercle is a short canal bone lying above the preopercle and containing the dorsal end of the opercular lateral line canal, which passes through it and enters the pterotic; and among centromochlines, this canal bone may vary. In some forms (as in Centromochlus perugiae, C. heckelii, and C. existimatus, a suprapreopercular ossification is absent, but in most forms it is present as a tube, completing the space between preopercle and the pterotic. In G. bockmanni, the suprapreopercle is not represented as a tube. This small canal bone is an incompletely ossified tube between the preopercle and the pterotic, with the bony portion located close to the preopercle. A fully ossified suprapreopercle was not detected in G. bockmanni. Glanidium bockmanni further differs from its congeners (albescens, ribeiroi, catharinensis, melanopterum, and leapardus in having a small adult size 29-48 mm SL (vs. 70-195 mm SL); lower jaw of equal size (vs. slightly prognathous); first nuchal plate absent (vs. present); low number of vertebrae 32 (vs. 3440); anal fin with 7 branched rays (vs. 8-11); and a less voluminous muscle adductor mandibulae A2 associated with a discrete concavity between sphenotic and pterotic (vs. thickened A2 associated with a quite pronounced concavity). It very closely resembles G. cesarpintoi , but can be distinguished from it due to larger post-cleithral process (20% SL vs. 16% SL); shorter mesethmoid (15% HL vs. 25% HL); adipose fin present (vs. absent); and pectoral-fin spine with antrorse spinules on anterior margin (vs. retrorse in cesarpintoi) (Ref. 56311).

Biologi     Daftar kata (contoh epibenthic)

The single specimen was captured in an area with gravel and rocky bottom, near the margin of the river (F. Bockmann, pers. comm.). The fishes from Bahia were captured by seine at night in a riverine beach in clear, shallow water with sand and gravel bottom in depth less than 1.70 m. Stomach contents of two specimens were partially digested fragments of insect larvae and nymphs (Ref. 56311).

Life cycle and mating behavior Maturities | Reproduksi, perkembang biakan | Spawnings | Egg(s) | Fecundities | Larva

rujukan utama Upload your references | Acuan | Koordinator : Ferraris, Jr., Carl J. | mitra

Sarmento-Soares, L.M. and P.A. Buckup, 2005. A new Glanidium from the Rio São Francisco Basin, Brazil (Siluriformes: Auchenipteridae: Centromochlinae). Copeia 2005(4):846-853. (Ref. 56311)

Status IUCN Red List (Ref. 130435)


CITES

Not Evaluated

CMS (Ref. 116361)

Not Evaluated

ancaman kepada manusia

  Harmless





penggunaan manusia

FAO - Publication: search | FishSource |

informasi lanjut

Trophic ecology
Bahan makanan
Diet compositions
Food consumptions
Food rations
Pemangsa
Ecology
Ekologi
Population dynamics
Growths
Max. ages / sizes
Length-weight rel.
Length-length rel.
ukuran frekuensi
Mass conversions
Recruitments
Abundances
Life cycle
Reproduksi, perkembang biakan
Maturities
Fecundities
Spawnings
Spawning aggregations
Egg(s)
Egg developments
Larva
Dinamika larva
Distribution
Negara-negara
Daerah-daerah FAO
Ecosystems
Kemunculan
Introduksi
BRUVS - Videos
Anatomy
Gill areas
Otak
Otoliths
Physiology
Body compositions
Nutrients
Oxygen consumptions
Swimming type
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Visual pigment(s)
Suara-suara ikan
Diseases / Parasites
Toxicities (LC50s)
Genetics
Genetika
Electrophoreses
Heritabilities
Human related
Aquaculture systems
profil budidaya air
Strain
Ciguatera cases
Stamps, coins, misc.
Outreach
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Taxonomy
Nama-nama umum
Sinonim (persamaan)
Morfologi
Morfometrik
Gambar
References
Acuan

Alat, peralatan

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Sumber internet

AFORO (otoliths) | Aquatic Commons | BHL | Cloffa | BOLDSystems | Websites from users | semak peneliti ikan | CISTI | Catalog of Fishes: Marga, Jenis | DiscoverLife | ECOTOX | FAO - Publication: search | Faunafri | Fishipedia | Fishtrace | GenBank: genom, Nukleotida | 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: pergi, Cari | World Records Freshwater Fishing | 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=0.00490 (0.00197 - 0.01219), b=3.10 (2.89 - 3.31), in cm total length, based on LWR estimates for this (Sub)family-body shape (Ref. 93245).
Trophic level (Ref. 69278):  3.2   ±0.4 se; based on size and trophs of closest relatives
Fishing Vulnerability (Ref. 59153):  Low vulnerability (10 of 100).