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Curculionichthys sabaji Roxo, Silva, Ochoa & Oliveira, 2015

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drawing shows typical species in Loricariidae.

Classification / Names ຊື່ສາມັນ | ຄຳສັບຄ້າຍຄືກັນ | Catalog of Fishes(ຕະກຸນ, ຊະນິດ) | 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 genussabaji: 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.

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

; ນ້ຳຈືດ ອາໄສຢູ່ໃກ້ໜ້າດິນໃຕ້ພື້ນທ້ອງນ້ຳ. Tropical

ການແຜ່ກະຈາຍ ປະເທດ | ເຂດ FAO | ລະບົບນິເວດ | ການປະກົດຕົວ | Point map | ການແນະນຳ | Faunafri

South America: Rio Xingu basin in Brazil.

ຂະໜາດ / ນ້ຳໜັກ / Age

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

Short description ຕົວທີ່ໃຊ້ໃນການຈຳແນກຊະນິດ | ສະລີລະວິທະຍາ | ການວັດແທກຮູບຮ່າງລັກສະນະພາຍນອກຂອງດິນ,ສັດ,ປາ…

ຄີຫຼັງຂອງປາ (ຄີອ່ອນ) (ທັງໝົດ) : 9; ຄີກົ້ນຂອງປາ: 5; ສັດທີ່ມີກະດູກສັນຫຼັງ: 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).

ຊີວະສາດ     ຄຳແປສັບ (ຕ.ຢ. epibenthic)

Life cycle and mating behavior ການຈະເລີນເຕັມໄວ | ການສືບພັນ | ການວາງໄຂ່ | ໄຂ່ | ຄວາມດົກຂອງໄຂ່ປາ | ຕົວອ່ອນ

Main reference Upload your references | ເອກະສານອ້າງອີງ | ຜູ້ປະສານງານ : Fisch-Muller, Sonia | ຜູ້ຮ່ວມມື

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 2024-2)


CITES

Not Evaluated

CMS (Ref. 116361)

Not Evaluated

Threat to humans

  Harmless





Human uses

ການປະມົງ: ທີ່ບໍ່ມີຄວາມສົນໃຈ
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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).
ຊັ້ນເຂດຮ້ອນ (Ref. 69278):  2.7   ±0.1 se; based on size and trophs of closest relatives
ຄວາມຢືດຢຸ່ນ (Ref. 120179):  ສູງ, ປະຊາກອນຕຳ່ສຸດທີ່ໃຊ້ເວລາສອງໜ້ອຍກວ່າ 15 ເດືອນ (Preliminary K or Fecundity.).
Fishing Vulnerability (Ref. 59153):  Low vulnerability (10 of 100).