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Curculionichthys coxipone Roxo, Silva, Ochoa & Oliveira, 2015

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Classification / Names Common names | Synonyms | Catalog of Fishes(genus, species) | ITIS | CoL | WoRMS | Cloffa

Teleostei (teleosts) > 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 genuscoxipone: The specific name coxipone refers to the Coxiponé indigenous people who live in the margins of Rio Cuiabá, near the municipality of Cuiabá in Mato Grosso State, Brazil. A noun in opposition.
Eponymy: The Coxiponé indigenous people inhabit the margins of Rio Cuiabá, Mato Grosso, Brazil, where this catfish occurs. (Ref. 128868), visit book page.

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

Freshwater; demersal. Tropical

Distribution Countries | FAO areas | Ecosystems | Occurrences | Point map | Introductions | Faunafri

South America: Rio Cuiaba drainage, Rio Paraguay basin in Brazil.

Size / Weight / Age

Maturity: Lm ?  range ? - ? cm
Max length : 2.8 cm SL male/unsexed; (Ref. 113800); 3.0 cm SL (female)

Short description Identification keys | Morphology | Morphometrics

Dorsal soft rays (total): 9; Anal soft rays: 6; Vertebrae: 29 - 30. Curculionichthys coxipone can be diagnosed from all congeners by having 29-30 vertebrae (vs. 28 in all other congeners). It is distinguished from all congeners, except Curculionichthys sabaji and C. paresi by having the cleithrum with an area free of odontodes (vs. cleithrum completely covered with odon¬todes). It further differs from all other species of Curculionichthys with the exception of C. oliveirai by having the anterior profile of the head rounded (vs. pointed); from C. piracanjuba, C. sagarana, and C. oliveirai by having lower lip with some papillae arranged in a medial longitudinal series extending posterior to dentaries through middle portion of lower lip (vs. lower lip with all papillae randomly distributed); from C. insperatus and C. oliveirai by having the caudal fin hyaline, with one dark stripe extending from the caudal peduncle base to the middle caudal fin rays, and dark chromatophores irregularly distributed almost forming one band (vs. caudal fin hyaline, with dark blotch limited to caudal peduncle base); from C. paresi by the absence of contrasting dark-brown geometric spots on the anterior region of the body (vs. presence of dark-brown geometric spots); from C. sabaji by the absence of several dark-brown spots distributed on the body (vs. presence of dark-brown spots); from C. oliveirai and C. coxipone by having the anterior profile of the head pointed (vs. rounded); from C. oliveirai by having 7?9 lateral abdomen plates (vs. 4?5 lateral abdomen plates); from C. paresi by having 9-13 dentary teeth (vs. 4?7); from C. oliveirai by having 6?9 lateral abdomen plates (vs. 4?5); from C. sagarana by absence of one unpaired platelets on dorsal portion of caudal peduncle (vs. presence of one unpaired platelets on dorsal portion of caudal peduncle); from C. piracanjuba by having some papillae on the lower lip arranged in a medial longitudinal series extending posterior to the dentaries through the middle portion of lower lip (vs. lower lip with all papillae randomly distributed) and by not having hypertrophied odontodes on the snout tip (vs. hypertrophied odontodes on the snout tip); 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). In addition, Curculionichthys coxipone is distinguished by the possession of the following characters: interorbital distance 33.8?37.8% of HL ( vs. 27.4?33.6% of HL in C. sagarana); dorsal fin spine 14.9?24.8% of SL (vs. 25.2?27.0% of SL in C. paresi); pectoral fin spine 19.0?25.2% of SL (vs. 27.0?30.1% of SL in C. paresi); mandibular ramus 8.2?12.5% of HL (vs. 6.0?8.0% of HL in C. paresi); and snout length 48.0?58.9% of HL (vs. 67.7?72.7% of HL in C. piracanjuba; 67.0?75.3% of HL in C. luteofrenatus) (Ref. 113800).

Biology     Glossary (e.g. epibenthic)

Life cycle and mating behavior Maturity | Reproduction | Spawning | Eggs | Fecundity | Larvae

Main reference Upload your references | References | Coordinator : Fisch-Muller, Sonia | Collaborators

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)

IUCN Red List Status (Ref. 130435: Version 2024-1)


CITES

Not Evaluated

CMS (Ref. 116361)

Not Evaluated

Threat to humans

  Harmless





Human uses

Fisheries: of no interest
FAO - Publication: search | FishSource |

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AFORO (otoliths) | Aquatic Commons | BHL | Cloffa | BOLDSystems | Websites from users | Check FishWatcher | CISTI | Catalog of Fishes: genus, species | DiscoverLife | ECOTOX | FAO - Publication: search | Faunafri | Fishipedia | Fishtrace | GenBank: genome, nucleotide | 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: Go, Search | World Records Freshwater Fishing | Zoobank | Zoological Record

Estimates based on models

Phylogenetic diversity index (Ref. 82804):  PD50 = 0.5005   [Uniqueness, from 0.5 = low to 2.0 = high].
Bayesian length-weight: a=0.00851 (0.00374 - 0.01935), b=3.09 (2.90 - 3.28), in cm total length, based on LWR estimates for this (Sub)family-body shape (Ref. 93245).
Trophic level (Ref. 69278):  2.4   ±0.1 se; based on size and trophs of closest relatives
Resilience (Ref. 120179):  High, minimum population doubling time less than 15 months (Preliminary K or Fecundity.).
Fishing Vulnerability (Ref. 59153):  Low vulnerability (10 of 100).