Curculionichthys sagarana

Curculionichthys sagarana Roxo, Silva, Ochoa & Oliveira, 2015

Uploaden van uw Foto's en video's
 Google afbeelding
Image of Curculionichthys sagarana
No image available for this species;
drawing shows typical species in Loricariidae.

Classificatie / Namen Lokale namen | Synoniemen | Catalog of Fishes(Genus, Soort(en)) | ITIS | CoL | WoRMS | Cloffa

> Siluriformes (Catfishes) > Loricariidae (Armored catfishes) > Hypoptopomatinae
Etymology: Curculionichthys: Derived from the from the Latin 'curculionem' (elongated snout) and from the Greek 'ichthys' (fishes), in reference to the relatively elongated snouts of the fish species included in this genus; sagarana: The specific name sagarana is derived from two words, 'saga' of Germanic origin, meaning heroic song, and 'rana' from Tupi-Guarani language, meaning similarity. The name is in reference to the book of a Brazilian author João Guimarães Rosa published in 1946 about the history of people from Minas Gerais State living in the region of Rio das Velhas.

Milieu: milieu / Klimaatzone / Diepte / verspreidingsgebied Ecologie

; zoet water demersaal. Tropical

Verspreiding Gebieden | FAO regio's | Ecosystemen | Voorkomen | Verspreidingskaart | Introducties | Faunafri

South America: Rio das Velhas drainage, Rio São Francisco basin in Brazil.

Grootte / Gewicht / Leeftijd

Maturiteit: Lm ?  range ? - ? cm
Max length : 2.3 cm SL mannelijk / geslacht onbekend; (Ref. 113800); 2.4 cm SL (female)

Korte beschrijving Determinatiesleutels | Morfologie | Morfometrie

Dorsale zachte stralen (totaal) : 9; Anale zachte stralen: 6; Wervels: 28. Curculionichthys sagarana can be distinguised from all congeners by the possession of one unpaired platelet on the dorsal portion of the caudal peduncle (vs. dorsal por¬tion of caudal peduncle without unpaired platelets). It further differs from all congeners, with the exception of Curculionichthys insperatus and C. luteofrenatus by having the caudal fin hyaline, with dark blotch limited to caudal peduncle base (vs. caudal fin hyaline, with one dark stripe extending from caudal peduncle base to the middle caudal fin rays, and for dark chromatophores irregularly distributed almost forming one or two bands); from C. insperatus, C. paresi and C. sabaji by having 15-19 premaxillary teeth (vs. 10?12 in C. insperatus; 6?10 in C. paresi and 7?12 in C. sabaji) and 12-18 dentary teeth (vs. 8?12 in C. insperatus, 4?7 in C. paresi and 7?12 in C. sabaji); from all congeners, except C. piracanjuba and C. oliveirai, by having all papillae on the lower lip randomly distributed (vs. lower lip with some papillae arranged in a medial longitudinal series extending posterior to dentaries through middle portion of lower lip); from C. oliveirai and C. coxipone by having the anterior profile of the head pointed (vs. rounded); from C. paresi by the absence of contrasting dark-brown geometric spots on the anterodorsal region of the body (vs. presence); from C. piracanjuba by having odontodes forming longitudinally aligned rows on the head and trunk (vs. odontodes not forming longitudinally aligned rows on the head and trunk); from C. sabaji, C. coxipone and C. paresi by having the cleithrum completely covered with odontodes (vs. the cleithrum with an area free of odontodes); from C. insperatus by having small, inconspicuous odontodes forming rows on the head and trunk (vs. large, conspicuous odontodes forming rows on the head and the trunk); from C. oliveirai by having 6?9 lateral abdomen plates (vs. 4?5); from C. piracanjuba by not having hypertrophied odontodes on the snout tip (vs. hypertrophied odontodes on the snout tip). In addition, Curculionichthys sagarana can be diagnosed by the following characters: deeper caudal peduncle (8.4-9.6 % of SL, vs. 10.8-12.5% of SL in C. oliveirai; 10.2-11.3% in C. paresi); greater head length (34.8-40.5% of SL, vs. 28.8-33.3% of SL in C. luteofrenatus; 27.9-32.2% of SL in C. piracanjuba); shorter snout (46.3-52.4% of HL, vs. 67.0-75.3% of HL in C. luteofrenatus; 67.7-72.7% of HL in C. piracanjuba); shorter interorbital width (27.4-33.6% of SL, vs. 33.3-45.4% of HL in C. luteofrenatus; 36.7-40.9% of HL in C. piracanjuba; 33.8-37.8% of HL in C. coxipone); deeper head (41.2-49.1% of HL, vs. 51.6-59.2% of HL in C. oliveirai); shorter dorsal-spine (19.9-24.4% of SL, vs. 25.2-27.0% of SL in C. paresi); and shorter pectoral-spine (21.5-25.2% of SL, vs. 27.0-30.1% of SL in C. paresi) (Ref. 113800).
Body shape (shape guide): elongated.

Biologie     Verklarende woordenlijst (bv. epibenthic)

Levenscyclus en paargedrag Maturiteit | Voortplanting | Paaien | Eieren | Fecunditeit | Larven

Hoofdreferentie Upload uw referenties | Referenties | Coördinator : Fisch-Muller, Sonia | Medewerkers

Roxo, F.F., G.S.C. Silva, L.E. Ochoa and C. Oliveira, 2015. Description of a new genus and three new species of Otothyrinae (Siluriformes, Loricariidae). Zookeys 534:103-134. (Ref. 113800)

Status op de Rode Lijst van het IUCN (Ref. 130435: Version 2025-2 (Global))

  Niet bedreigd (LC) ; Date assessed: 13 November 2020

CITES

Not Evaluated

CMS (Ref. 116361)

Not Evaluated

Gevaar voor de mens

  Harmless





Gebruik door de mens

Visserij: van geen belang
FAO - Publication: search | FishSource |

Meer informatie

Trofische ecologie
Voedsel (prooien)
Dieetsamenstelling
Voedselconsumptie
Voedselrantsoenen
Predatoren
Ecologie
Ecologie
Populatiedynamica
Groeiparameters
Max. leeftijden / maten
Lengte-gewicht rel.
Lengte-lengte rel.
Lengtefrequenties
Massaconversie
Rekrutering
Abundantie
Levenscyclus
Voortplanting
Maturiteit
Rijpheid/kieuwen rel.
Fecunditeit
Paaien
Paaibestanden
Eieren
Ontwikkeling van de eieren
Larven
Larvale populatiedynamiek
Verspreiding
Gebieden
FAO regio's
Ecosystemen
Voorkomen
Introducties
BRUVS - Video's
Anatomie
Kieuwoppervlak
Hersenen
Otoliet
Fysiologie
Lichaamssamenstelling
Voedingsstoffen
Zuurstofverbruik
Type zwemmen
Zwemsnelheid
Visuele pigmenten
Vis geluid
Ziekten en parasieten
Toxiciteit (LC50)
Genetica
genoom
Genetica
Heterozygositeit
Erfelijkheid
Genetische diversiteit
Menselijk gerelateerd
Aquacultuursystemen
Aquacultuurprofielen
Kweeklijnen
Ciguatera gevallen
Postzegels, munten, diversen.
Outreach
Medewerkers
Taxonomie
Lokale namen
Synoniemen
Morfologie
Morfometrie
Afbeeldingen
Referenties
Referenties

Tools

E-boek | Veldgids | Lengtefrequentie Tool | Levenscyclus tool | Verspreidingskaart | Vangst-MSY |

Speciale rapporten

Bekijk gegevens voor het houden in een aquarium | Bekijk Fact Sheets voor de soort | Bekijk Aquacultuur Fact Sheets

Download XML

Overzichtspagina | Puntgegevens | Lokale namen | Foto's

Internetbronnen

AFORO (otoliths) | Aquatic Commons | BHL | Cloffa | Websites from users | Bekijk FishWatcher | CISTI | Catalog of Fishes: Genus, Soort(en) | 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: ga naar, zoek | World Records Freshwater Fishing | Zoobank | Zoological Record

Schattingen op basis van modellen

Fylogenetische diversiteitsindex
(Ref. 82804) 		PD50 = 0.5001 [Uniqueness, from 0.5 = low to 2.0 = high].
Bayesian length-weight a=0.00977 (0.00436 - 0.02192), b=3.06 (2.87 - 3.25), in cm total length, based on LWR estimates for this (Sub)family-body shape (Ref. 93245).
Trofisch niveau
(Ref. 69278) 		2.6   ±0.1 se; based on size and trophs of closest relatives
Weerstandsvermogen
(Ref. 120179) 		Hoog, minimale populatieverdubbelingstijd minder dan 15 maanden (Preliminary K or Fecundity.).
Kwetsbaarheid van de visserij
(Ref. 59153) 		Low vulnerability (10 of 100). 🛈