Ernstichthys taquari

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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.

Klassificering / Namn Populärnamn | synonymer | Catalog of Fishes(Släkte, Arter) | 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.

Miljö: miljö / Klimatzon / djupintervall / distributionsområde Ekologi

; sötvatten bottenlevande. Tropical

Utbredning Territorier | FAO områden | Ekosystem | Förekomster | Prickkarta | Utplanteringar | Faunafri

South America: Brazil.

Storlek / Vikt / Ålder

Könsmognad: Lm ?  range ? - ? cm
Max length : 2.3 cm SL hane/ej könsbestämd; (Ref. 124573)

Kort beskrivning Bestämningsnycklar | Morfologi | Morfometri

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     Ordlista (t.ex. 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).

Livscykel och parningsbeteende Könsmognad | Reproduktion | Lek | Ägg | Fekunditet | Larver

Huvudreferens Ladda upp dina referenser | referenser | Koordinator : Friel, John P. | Medarbetare

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 på IUCN:s rödlista (Ref. 130435: Version 2025-2 (Global))


CITES

Not Evaluated

CMS (Ref. 116361)

Not Evaluated

Hot mot människor

  Harmless





Mänskliga användningsområden

FAO - Publication: search | FishSource |

Ytterligare information

Trofisk ekologi
Livsmedelsartiklar (preys)
Födosammansättning
Födointag
Matransoner
Predatorer
Ekologi
Ekologi
Populationsdynamik
Tillväxtparametrar
Max. åldrar / storlekar
Längd-vikt rel.
Längd-längd rel.
Längd-frekvenser
Massakonvertering
Rekrytering
Abundans
Livscykel
Reproduktion
Könsmognad
Mognad/Gills rel.
Fekunditet
Lek
Lekande aggregat
Ägg
Utveckling av ägg
Larver
Larvdynamik
Utbredning
Territorier
FAO områden
Ekosystem
Förekomster
Utplanteringar
BRUVS - Videor
Anatomi
Gälyta
Hjärna
Otolit
Fysiologi
Kroppssammansättning
Näringsämnen
Syreförbrukning
Typ av simning
Simhastighet
Visuella pigment
Ljud från fisk
Sjukdomar & Parasiter
Toxicitet (LC50)
Genetik
Genom
Genetik
Heterozygositet
Ärftlighet
Genetisk mångfald
Människorelaterad
Vattenbrukssystem
Vattenbruksprofiler
Avelslinjer
Ciguatera-fall
Frimärken, mynt, diverse.
Uppsökande verksamhet
Medarbetare
Taxonomi
Populärnamn
synonymer
Morfologi
Morfometri
Bilder
referenser
referenser

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Särskilda rapporter

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Internet-källor

AFORO (otoliths) | Aquatic Commons | BHL | Cloffa | Websites from users | Check FishWatcher | CISTI | Catalog of Fishes: Släkte, Arter | 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: Go, sök | World Records Freshwater Fishing | Zoobank | Zoologiskt register

Uppskattningar baserade på modeller

Index för fylogenetisk mångfald (Ref. 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).
Trofisk nivå (Ref. 69278):  3.0   ±0.3 se; based on size and trophs of closest relatives
Sårbarhet i fisket (Ref. 59153):  Low vulnerability (10 of 100). 🛈