Paracanthopoma saci

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Paracanthopoma saci Dagosta & de Pinna, 2021

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Image of Paracanthopoma saci
No image available for this species;
drawing shows typical species in Trichomycteridae.

klasifikasi / Names Nama-nama umum | Sinonim (persamaan) | Catalog of Fishes(Marga, Jenis) | ITIS | CoL | WoRMS | Cloffa

> Siluriformes (Catfishes) > Trichomycteridae (Pencil or parasitic catfishes) > Vandelliinae
Etymology: Paracanthopoma: Greek, para = the side of + Greek, akantha = thorn + Greek, poma, -atos = cover, operculum (Ref. 45335).

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

; air tawar dasar (demersal). Tropical

Penyebaran Negara-negara | Daerah-daerah FAO | Ecosystems | Kemunculan | Point map | Introduksi | Faunafri

South America: Brazil.

Size / Weight / umur

Maturity: Lm ?  range ? - ? cm
Max length : 2.2 cm SL jantan/; (Ref. 124573)

deskripsi pendek Morfologi | Morfometrik

This species is distinguished from Paracanthopoma parva by the following characters: a short and anteriorly-displaced opercular patch of odontodes, leaving a large posterior free area of integument continuous with the rest of the head integument around it (in dorsal view the posterior tips of the opercular odontodes do not reach the base of the pectoral fin); pelvic fin 3 (vs. 5); opercle without an ascending process (vs. with ascending process); caudal peduncle spatulate by hypertrophied series of 22?29 (upper) and 20?29 (lower) procurrent caudal-fin rays (vs. caudal peduncle narrow, with 15-19 upper and 14-18 lower rays); median premaxillary dentition feeble, with 3 delicate teeth (vs. median premaxillary dentition robust, 9 large strong teeth); supraorbital canals opening as two separate s6 pores (vs. canals fused at midline and opening as single median s6 pore); caudal fin slightly convex or truncate, with round edges (the apparent emarginated margin is a preservation artifact) (vs. bilobed or emarginate, concave); supraoccipital no anterior median process (vs. supraoccipital with produced anterior process); origins of dorsal and anal fins approximately at same vertical (vs. origin of dorsal fin clearly anterior to vertical through origin of anal fin) (Ref. 124573).

Biologi     Daftar kata (contoh epibenthic)

The Rio Taquarizinho is ca. 15 m wide at the collection locality; the water is clear, slightly milky and with moderate current. Specimens were collected by seining on sand banks in the middle of the river, especially in sectors shaded by riparian vegetation. There was no aquatic vegetation and depth of collection ranged from 30-150 cm. This species is sympatric with Paravandellia oxyptera, both are relatively abundant at the type locality. These two species are psammophilic, but with different microhabitat preferences where P. saci favors fine sand, while P. oxytera prefers sectors with coarser granulation. Segregation is not complete however, and occasionally they were captured together in the same net. Some female specimens have large eggs, approximately eye-sized or slightly larger, visible by transparency. Eggs distributed along ventral margin of hypaxial musculature from shortly posterior to end of pectoral fin to nearly end of abdominal cavity, with approximately 20 eggs visible in lateral layer of each side (certainly more in inner portions of gonad) (Ref. 124573).

Life cycle and mating behavior Kematangan | Reproduksi, perkembang biakan | Pemijahan | telur-telur | Fecundity | Larva

rujukan utama Upload your references | Acuan | Koordinator : Pinna, Mário de | mitra

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 IUCN Red List (Ref. 130435)


CITES

Not Evaluated

CMS (Ref. 116361)

Not Evaluated

ancaman kepada manusia

  Harmless





penggunaan manusia

FAO - Publication: search | FishSource |

informasi lanjut

Negara-negara
Daerah-daerah FAO
Ecosystems
Kemunculan
Introduksi
Stocks
Ekologi
Makanan
Bahan makanan
Konsumsi makanan
Jatah
Nama-nama umum
Sinonim (persamaan)
metabolisme
Pemangsa
Ekotoksikologi
Reproduksi, perkembang biakan
Kematangan
Pemijahan
Spawning aggregation
Fecundity
telur-telur
pekembangan telor
Umur / Saiz
Pertumbuhan
panjang-berat
panjang-panjang
ukuran frekuensi
Morfometrik
Morfologi
Larva
Dinamika larva
pemulihan
Kelimpahan
BRUVS
Acuan
Budidaya air
profil budidaya air
Strain
Genetika
Electrophoreses
Diturunkan
Penyakit-penyakit
Pengolahan
Nutrients
Mass conversion
mitra
Gambar
Stamps, Coins Misc.
Suara-suara
Ciguatera
Kecepatan
Tipe renang
Area insang
Otoliths
Otak
Penglihatan / visi

Alat, peralatan

laporan khas

muat turun XML

Sumber internet

AFORO (otoliths) | Aquatic Commons | BHL | Cloffa | BOLDSystems | Websites from users | semak peneliti ikan | CISTI | Catalog of Fishes: Marga, Jenis | DiscoverLife | ECOTOX | FAO - Publication: search | Faunafri | Fishipedia | Fishtrace | GenBank: genom, Nukleotida | 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: pergi, Cari | World Records Freshwater Fishing | Zoobank | Zoological Record

Estimates based on models

Phylogenetic diversity index (Ref. 82804):  PD50 = No PD50 data   [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).
Trophic level (Ref. 69278):  3.2   ±0.6 se; based on size and trophs of closest relatives
Fishing Vulnerability (Ref. 59153):  Low vulnerability (10 of 100).