Ernstichthys taquari

Ernstichthys taquari Dagosta & de Pinna, 2021

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Image of Ernstichthys taquari
No image available for this species;
drawing shows typical species in Aspredinidae.

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

> Siluriformes (Catfishes) > Aspredinidae (Banjo catfishes) > Hoplomyzontinae
Etymology: taquari: Named for rio Taquari, a word of Tupi language origin (takwa’ri) combining ta’kwara (a common name for bamboo-like plants of family Poaceae) plus ‘i’ for diminutive; a noun in apposition.
Eponymy: Dr Adolfo (also spelled Adolf) Ernst (1832–1899) was a biologist, born in Prussia and a graduate of the University of Berlin. [...] (Ref. 128868), visit book page.

Lingkungan: lingkungan / zona iklim / kisaran kedalaman / jangkauan distribusi Ekologi

; air tawar dasar (demersal). Tropical

Penyebaran Wilayah | Daerah-daerah FAO | Ekosistem | Kemunculan | peta titik | Introduksi | Faunafri

South America: Brazil.

Ukuran / Berat / umur

Kematangan: Lm ?  range ? - ? cm
Max length : 2.3 cm SL jantan/; (Ref. 124573)

deskripsi pendek Kunci identifiaksi (pengenalan) | Morfologi | Morfometrik

This species is distinguished from all its congeners by the following characters: relatively narrow bilateral bony shields on dorsal and ventral series, these do not overlap or contact each other anywhere in both series (vs. adjacent shields contacting or overlapping along most or entire series; this trait also separates this species from most hoplomyzontine species except those of Hoplomyzon); with seven or eight serrations on the posterior margin of the pectoral spine (vs. 10-18); pectoral-fin spine only slightly larger than subsequent soft rays, there is a gradual transition between the spine and the rest of fin (vs. spine 25% longer or more than soft rays, leaving a large portion of protruding spine without corresponding fin web distally); differs from E. megistus by having a well-developed rictal barbel (vs. no barbel or reduced to bump); differs from E. intosus by the unbranched maxillary barbel (vs. with thread-like secondary barbels); no dentations along the anterior margin of the pectoral fin (vs. with dentations); with two pairs of stout and regularly-positioned mental barbels (vs. over 100 thread-like and uniformly distributed barbels); D i+4 (vs. i+7); A i+6 anal-fin rays (vs. viii+4); basipterygium entirely hidden in integument (vs. anterolateral arm of basipterygium exposed on the skin, forming rugose shield) (Ref. 124573).
Cross section: flattened.

Biologi     Daftar kata (contoh epibenthic)

Collected in a white water river, with moderate water flow, over rock and sand. Its habitat is not the deep bottom of a large river, but rather a small river accessible by hand-seining. Aquatic macrophytes were present in some sites and riparian forest was well preserved; all specimens were collected in a shaded sector covered with dense vegetation and large rocks on the bottom (Ref. 124573).

Siklus hidup dan perilaku kawin Kematangan | Reproduksi, perkembang biakan | Pemijahan | telur-telur | Fekunditas | Larva

rujukan utama Unggah referensi Anda | Acuan | Koordinator : Friel, John P. | mitra

Dagosta, F.C.P. and M. de Pinna, 2021. Two new catfish species of typically Amazonian lineages in the Upper Rio Paraguay (Aspredinidae: Hoplymyzontinae and Trichomycteridae: Vandelliinae), with a biogeographic discussion. Pap. Avulsos Zool. 61:e20216147. (Ref. 124573)

Status IUCN Red List (Ref. 130435: Version 2025-2 (Global))


CITES

Not Evaluated

CMS (Ref. 116361)

Not Evaluated

ancaman kepada manusia

  Harmless





penggunaan manusia

FAO - Publication: search | FishSource |

informasi lanjut

Ekologi trofik
Item makanan (mangsa)
Komposisi makanan
Konsumsi makanan
Ransum makanan
Pemangsa
Ekologi
Ekologi
Dinamika populasi
Parameter pertumbuhan
Maks. usia / ukuran
Panjang-berat rel.
Panjang-panjang rel.
ukuran frekuensi
Konversi massa
pemulihan
Kelimpahan
Siklus hidup
Reproduksi, perkembang biakan
Kematangan
Kedewasaan / insang rel.
Fekunditas
Pemijahan
Agregasi pemijahan
telur-telur
pekembangan telor
Larva
Dinamika larva
Penyebaran
Wilayah
Daerah-daerah FAO
Ekosistem
Kemunculan
Introduksi
BRUVS - Video
Anatomi
Area insang
Otak
Otolith
Fisiologi
Komposisi tubuh
Nutrisi
Konsumsi oksigen
Jenis renang
Kecepatan berenang
Pigmen visual
Suara ikan
Penyakit & Parasit
Toksisitas (LC50)
Genetika
genom
Genetika
Heterozigositas
Diturunkan
Keanekaragaman Genetik
Yang berhubungan dengan manusia
Sistem akuakultur
profil budidaya air
Strain
Kasus Ciguatera
Perangko, koin, dll.
Penjangkauan
mitra
Taksonomi
Nama-nama umum
Sinonim (persamaan)
Morfologi
Morfometrik
Gambar
Acuan
Acuan

Alat, peralatan

laporan khas

muat turun XML

Sumber internet

AFORO (otoliths) | Aquatic Commons | BHL | Cloffa | Websites from users | semak peneliti ikan | CISTI | Catalog of Fishes: Marga, Jenis | DiscoverLife | ECOTOX | FAO - Publication: search | Faunafri | Fishipedia | Fishtrace | GloBI | Google Books | Google Scholar | Google | IGFA World Record | OneZoom | Open Tree of Life | Otolith Atlas of Taiwan Fishes | PubMed | Reef Life Survey | Socotra Atlas | TreeBase | Tree of Life | Wikipedia: pergi, Cari | World Records Freshwater Fishing | Zoobank | Catatan Zoologi

Estimasi berdasarkan model

Indeks keanekaragaman filogenetik
(Acuan 82804)
PD50 = 0.5312 [Uniqueness, from 0.5 = low to 2.0 = high].
Bayesian length-weight a=0.00389 (0.00180 - 0.00842), b=3.12 (2.94 - 3.30), in cm total length, based on all LWR estimates for this body shape (Ref. 93245).
Tingkat Trofik
(Acuan 69278)
3.0   ±0.3 se; based on size and trophs of closest relatives
Kerentanan Penangkapan Ikan
(Ref. 59153)
Low vulnerability (10 of 100). 🛈