Curculionichthys sabaji

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Curculionichthys sabaji Roxo, Silva, Ochoa & Oliveira, 2015

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Image of Curculionichthys sabaji
No image available for this species;
drawing shows typical species in Loricariidae.

klasifikasi / Names Nama-nama umum | Sinonim (persamaan) | Catalog of Fishes(Marga, Jenis) | 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)..

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: Rio Xingu basin in Brazil.

Size / Weight / umur

Maturity: Lm ?  range ? - ? cm
Max length : 2.4 cm SL jantan/; (Ref. 113800)

deskripsi pendek Morfologi | Morfometrik

duri punggung lunak (Keseluruhan (total)): 9; Sirip dubur lunak: 5; vertebrata, bertulang belakang: 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).

Biologi     Daftar kata (contoh epibenthic)

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

rujukan utama Upload your references | Acuan | Koordinator : Fisch-Muller, Sonia | mitra

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 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

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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 = 0.5005   [Uniqueness, from 0.5 = low to 2.0 = high].
Bayesian length-weight: a=0.00759 (0.00337 - 0.01709), b=3.12 (2.93 - 3.31), in cm total length, based on LWR estimates for this (Sub)family-body shape (Ref. 93245).
Trophic level (Ref. 69278):  2.7   ±0.1 se; based on size and trophs of closest relatives
Daya lenting (Ref. 120179):  Tinggi, Waktu penggandaan populasi minimum kurang dari 15 bulan (Preliminary K or Fecundity.).
Fishing Vulnerability (Ref. 59153):  Low vulnerability (10 of 100).