Curculionichthys sabaji

Curculionichthys sabaji Roxo, Silva, Ochoa & Oliveira, 2015

Envoyez vos Photos et vidéos
 Images Google
Image of Curculionichthys sabaji
No image available for this species;
drawing shows typical species in Loricariidae.

Classification / Noms Noms communs | Synonymes | Catalog of Fishes(Genre, Espèce) | 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; sabaji: Named for Dr. Mark Henry Sabaj Pérez, Collection Manager of Ichthyology, Academy of Natural Sciences of Philadelphia, in recognition of his dedication and contributions to study of Neotropical fishes especially from Rio Xingu basin (iXingu Project).
Eponymy: Dr Mark Henry Sabaj Pérez (d: 1969) is an ichthyologist and collection manager of fishes at the Academy of Natural Sciences of Philadelphia (2000–present). [...] (Ref. 128868), visit book page.

Environnement : milieu / zone climatique / profondeur / gamme de distribution Écologie

; eau douce démersal. Tropical

Distribution Territoires | Zones FAO | Écosystèmes | Occurrences | Carte par point | Introductions | Faunafri

South America: Rio Xingu basin in Brazil.

Taille / Poids / Âge

Maturité: Lm ?  range ? - ? cm
Max length : 2.4 cm SL mâle / non sexé; (Ref. 113800)

Description synthétique Clés d'identification | Morphologie | Morphométrie

Rayons mous dorsaux (Total) : 9; Rayons mous anaux: 5; Vertèbres: 28. Curculionichthys sabaji is distinguished from all congeners by possessing several dark-brown spots distributed on the body (vs. a variety of pigment patterns, but none of which includes dark-brown spots). It also differs from all con¬geners, except C. coxipone and C. paresi by having the cleithrum with an area free of odontodes (vs. cleithrum completely covered with odontodes). Other characters useful to further diagnosed this species from other congengers include the following: some papillae of the lower lip arranged in a medial longitudinal series extending posterior to dentaries through the middle portion of the lower lip (vs. lower lip with all papillae randomly distributed in from C. piracanjuba, C. sagarana, and C. oliveirai); anterior profile of the head pointed (vs. rounded in C. coxipone and C. oliveirai); odontodes forming longitudinally aligned rows on head and trunk (vs. odontodes not forming longitudinally aligned rows on head and trunk in C. piracanjuba); small, inconspicuous odontodes forming rows on the head and trunk (vs. large, conspicuous odontodes forming rows on the head and the trunk in C. insperatus); caudal fin hyaline, with one dark strip extending from caudal peduncle base to the median caudal fin rays, and dark chromatophores irregular distributed almost forming two bands (vs. caudal fin hyaline, with dark blotch limited to caudal peduncle base in C. insperatus and C. sagarana); absence of one unpaired platelet on the dorsal portion of caudal peduncle (vs. one unpaired platelet on the dorsal portion of the caudal peduncle in C. sagarana); 6?9 lateral abdomen plates (vs. 4?5 lateral abdomen plates in C. oliveirai); absence of contrasting dark geometric spots on the anterodorsal region of body (vs. pres¬ence of geometric spots in C. paresi); not having hypertrophied odontodes on the snout tip (vs. hypertrophied odontodes on the snout tip in C. piracanjuba). In addition, Curculionichthys sabaji can be distinguished by having a shorter dorsal fin spine (18.5?22.7% of SL, vs. 25.2?27.0% of SL in C. paresi; 23.2?26.9% of SL in C. insperatus); a shorter pectoral-fin spine (18.9?23.4% of SL, vs. 27.0?30.1% of SL in C. paresi); a deeper caudal peduncle (7.0?10.0% of SL, vs. 10.8?12.5% of SL in C. oliveirai; 10.2?11.3% of SL in C. paresi); a deeper head (40.9?49.1% of HL, vs. 51.6?59.2% of HL in C. oliveirai); a longer head (34.3?38.6% of SL, vs. 27.9?32.2% of SL in C. piracanjuba; 28.8?33.3% of SL in C. luteofrenatus); a shorter snout (45.5?56.9% of HL, vs. 67.7?72.7% of HL in C. piracanjuba; 67.0?75.3% of HL in C. luteofrenatus) and a shorter interorbital width (30.3?35.7% of HL, vs. 36.7?40.9% of HL in C. piracanjuba; 67.0?75.3% of HL in C. luteofrenatus) (Ref. 113800).
Body shape (shape guide): elongated.

Biologie     Glossaire (ex. epibenthic)

Cycle de vie et comportement reproducteur Maturité | Reproduction | Frai | Œufs | Fécondité | Larves

Référence principale Téléchargez vos références | Références | Coordinateur : Fisch-Muller, Sonia | Collaborateurs

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)

Statut dans la liste rouge de l'IUCN (Ref. 130435: Version 2025-2 (Global))


CITES

Not Evaluated

CMS (Ref. 116361)

Not Evaluated

Menace pour l'homme

  Harmless





Utilisations par l'homme

Pêcheries: sans intérêt
FAO - Publication: search | FishSource |

Plus d'informations

Écologie trophique
Aliments (proies)
Composition du régime alimentaire
Consommation alimentaire
Rations alimentaires
Prédateurs
Écologie
Écologie
Dynamique des populations
Paramètres de croissance
Âges / tailles maximales
Longueur-poids rel.
Rel. longueur-longueur.
Fréquences de longueurs
Conversion de masse
Recrutement
Abondance
Cycle de vie
Reproduction
Maturité
Maturité/épines rel.
Fécondité
Frai
Agrégats de frai
Œufs
Développement de l'œuf
Larves
Dynamique des populations larvaires
Distribution
Territoires
Zones FAO
Écosystèmes
Occurrences
Introductions
BRUVS - Vidéos
Anatomie
Surface branchiale
Cerveau
Otolithe
Physiologie
Composition corporelle
Nutriments
Consommation d'oxygène
Type de natation
Vitesse de nage
Pigments visuels
Son de poisson
Maladies et parasites
Toxicité (CL50)
Génétique
génôme
Génétique
Hétérozygotie
Héritabilité
Diversité génétique
Liées à l'homme
Systèmes d'aquaculture
Profils d'aquaculture
Souches
Cas de ciguatera
Timbres, pièces de monnaie, divers
Sensibilisation
Collaborateurs
Taxonomie
Noms communs
Synonymes
Morphologie
Morphométrie
Images
Références
Références

Outils

E-book | Guide de terrain | Générateur de fréquences de longueur | Outil de dynamique de population | Carte par point | Capture-MSY |

Articles particuliers

Maintenance en aquarium | Articles sur l'espèce | Rapports d'aquaculture

Télécharger en XML

Page de résumé | Coordonnées géographiques | Noms communs | Photos

Sources Internet

AFORO (otoliths) | Aquatic Commons | BHL | Cloffa | Websites from users | FishWatcher | CISTI | Catalog of Fishes: Genre, Espèce | 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 | Arbre de Vie | Wikipedia: aller à, chercher | World Records Freshwater Fishing | Zoobank | Zoological Record

Estimations basées sur des modèles

Indice de diversité phylogénétique
(Réf. 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).
Niveau trophique
(Réf. 69278) 		2.7   ±0.1 se; based on size and trophs of closest relatives
Résilience
(Réf. 120179) 		Haut, temps minimum de doublement de population inférieur à 15 mois (Preliminary K or Fecundity.).
Vulnérabilité de la pêche
(Ref. 59153) 		Low vulnerability (10 of 100). 🛈