You can sponsor this page

Pareiorhina pelicicei Azevedo-Santos & Roxo, 2015

Upload your photos and videos
Pictures | Google image
Image of Pareiorhina pelicicei
Pareiorhina pelicicei
Picture by Azevedo-Santos, V.M.

Classification / Names Populärnamn | synonymer | Catalog of Fishes(Släkte, Arter) | ITIS | CoL | WoRMS | Cloffa

> Siluriformes (Catfishes) > Loricariidae (Armored catfishes) > Hypoptopomatinae
Etymology: Pareiorhina: Greek, pareia = jaw + Greek, rhinos = nose (Ref. 45335)pelicicei: Named for Dr. Fernando Mayer Pelicice, from Universidade Federal do Tocantins.
Eponymy: Fernando Mayer Pelicice of the Universidade Federal do Tocantins, Brazil, was honoured in the binomial for his scientific contributions to fish ecology and the impacts of dams on Neotropical fishes. [...] (Ref. 128868), visit book page.

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

; sötvatten pelagiska. Tropical

Utbredning Länder | FAO områden | Ekosystem | Förekomster | Point map | Utplanteringar | Faunafri

South America: Brazil.

Size / Vikt / Age

Maturity: Lm ?  range ? - ? cm
Max length : 4.7 cm SL hane/ej könsbestämd; (Ref. 100791); 4.2 cm SL (female)

Short description Bestämningsnycklar | Morfologi | Morfometri

Mjukstrålar i ryggfenan (totalt) : 7; Mjukstrålar i analfenan: 5; Ryggkotor: 29. This species is distinguished from P. carrancas and P. hyptiorhachis by the absence of a postdorsal ridge (vs. presence of a postdorsal ridge); differs from all its congeners, except P. hyptiorhachis, by having less vertebrae, 29 (vs. 30 in P. brachyrhyncha and P. cepta; 31 in P. carrancas and P. rudolphi); differs from P. carrancas, P. hyptiorhachis and P. rudolphi by having teeth with a minute lateral cusp (vs. unicuspid teeth); differs from P. brachyrhyncha and P. hyptiorhachis by having the anterior profile of the head elliptical in dorsal view (vs. rounded); differs from P. brachyrhyncha by having the tip of the snout naked (vs. the tip of the snout completely covered with small odontodes), a lower predorsal length (41.0-44.8 mm SL vs. 45.6-48.9 mm SL), higher number of premaxillary teeth (35-48 vs. 28-36), and higher number of dentary teeth (33-49 vs. 26-36); differs from P. cepta by lacking small plates distributed on the thorax and abdomen (Ref. 100791).

Biologi     Ordlista (t.ex. epibenthic)

This species was collected in a stream with clear water, on bedrock and gravel, and with partially submerged riparian vegetation. Usually, individuals were always found in lotic environments associated with rocks, never in lentic (i.e., pools that formed on stretches of the creek). Some areas of the gallery forest were partially preserved, and penetration of light was scarce. Another species sampled syntopically were Astyanax scabripinnis group and Trichomycterus spp. Also observed were amphibian larvae, spiders, leeches, aquatic insects (Coleoptera; Hemiptera) and larval stages of insects (Diptera; Trichoptera; Megaloptera) (Ref. 100791).

Life cycle and mating behavior Könsmognad | Reproduktion | Lek | Ägg | Fecundity | Larver

Main reference Upload your references | referenser | Koordinator : Fisch-Muller, Sonia | Medarbetare

Azevedo-Santos, V.M. and F.F. Roxo, 2015. A new species of the genus Pareiorhina (Teleostei: Siluriformes: Loricariidae) from the upper rio Paraná basin, southeastern Brazil. Zootaxa 3937(2):377-384. (Ref. 100791)

IUCN Red List Status (Ref. 130435: Version 2024-2)

  Data deficient (DD) ; Date assessed: 14 December 2020

CITES

Not Evaluated

CMS (Ref. 116361)

Not Evaluated

Threat to humans

  Harmless





Human uses

FAO - Publication: search | FishSource |

Ytterligare information

Trophic ecology
Födoslag
Födosammansättning
Födointag
Food rations
Predatorer
Ecology
Ekologi
Population dynamics
Tillväxtparametrar
Max. ages / sizes
Length-weight rel.
Length-length rel.
Length-frequencies
Mass conversion
Rekrytering
Abundans
Life cycle
Reproduktion
Könsmognad
Maturity/Gills rel.
Fecundity
Lek
Spawning aggregations
Ägg
Egg development
Larver
Larvdynamik
Distribution
Länder
FAO områden
Ekosystem
Förekomster
Utplanteringar
BRUVS - Videos
Anatomy
Gälyta
Brain
Otolith
Physiology
Body composition
Nutrients
Syreförbrukning
Swimming type
Simhastighet
Visual pigments
Fish sound
Diseases & Parasites
Toxicity (LC50s)
Genetics
Genetik
Heterozygosity
Ärftlighet
Human related
Aquaculture systems
Vattenbruksprofiler
Avelslinjer
Ciguatera cases
Stamps, coins, misc.
Outreach
Medarbetare
Taxonomy
Populärnamn
synonymer
Morfologi
Morfometri
Bilder
References
referenser

Verktyg

Special reports

Download XML

Internet-källor

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

Estimates based on models

Phylogenetic diversity index (Ref. 82804):  PD50 = 0.5156   [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).
Resiliens (Ref. 120179):  Hög, lägsta populationsfördubblingstid mindre än 15 månader (Preliminary K or Fecundity.).
Fishing Vulnerability (Ref. 59153):  Low vulnerability (10 of 100).