Curculionichthys sagarana

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Curculionichthys sagarana Roxo, Silva, Ochoa & Oliveira, 2015

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drawing shows typical species in Loricariidae.

分類 / Names 共通名の | 類義語 | Catalog of Fishes(部類, ) | 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.;  sagarana: The specific name sagarana is derived from two words, 'saga' of Germanic origin, meaning heroic song, and 'rana' from Tupi-Guarani language, meaning similarity. The name is in reference to the book of a Brazilian author João Guimarães Rosa published in 1946 about the history of people from Minas Gerais State living in the region of Rio das Velhas..

Environment: milieu / climate zone / depth range / distribution range 生態学

; 新鮮な水 底生の. Tropical

分布 国々 | 国連食糧農業機関の区域 | エコシステム | 事件 | Point map | 導入 | Faunafri

South America: Rio das Velhas drainage, Rio São Francisco basin in Brazil.

サイズ / 重さ / 年齢

Maturity: Lm ?  range ? - ? cm
Max length : 2.3 cm SL オス/雌雄の選別がない; (Ref. 113800); 2.4 cm SL (female)

簡単な記述 形態学 | 形態計測学

背鰭 (合計): 9; 臀鰭: 6; 脊つい: 28. Curculionichthys sagarana can be distinguised from all congeners by the possession of one unpaired platelet on the dorsal portion of the caudal peduncle (vs. dorsal por¬tion of caudal peduncle without unpaired platelets). It further differs from all congeners, with the exception of Curculionichthys insperatus and C. luteofrenatus by having the caudal fin hyaline, with dark blotch limited to caudal peduncle base (vs. caudal fin hyaline, with one dark stripe extending from caudal peduncle base to the middle caudal fin rays, and for dark chromatophores irregularly distributed almost forming one or two bands); from C. insperatus, C. paresi and C. sabaji by having 15-19 premaxillary teeth (vs. 10?12 in C. insperatus; 6?10 in C. paresi and 7?12 in C. sabaji) and 12-18 dentary teeth (vs. 8?12 in C. insperatus, 4?7 in C. paresi and 7?12 in C. sabaji); from all congeners, except C. piracanjuba and C. oliveirai, by having all papillae on the lower lip randomly distributed (vs. lower lip with some papillae arranged in a medial longitudinal series extending posterior to dentaries through middle portion of lower lip); from C. oliveirai and C. coxipone by having the anterior profile of the head pointed (vs. rounded); from C. paresi by the absence of contrasting dark-brown geometric spots on the anterodorsal region of the body (vs. presence); from C. piracanjuba by having odontodes forming longitudinally aligned rows on the head and trunk (vs. odontodes not forming longitudinally aligned rows on the head and trunk); from C. sabaji, C. coxipone and C. paresi by having the cleithrum completely covered with odontodes (vs. the cleithrum with an area free of odontodes); 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); from C. oliveirai by having 6?9 lateral abdomen plates (vs. 4?5); from C. piracanjuba by not having hypertrophied odontodes on the snout tip (vs. hypertrophied odontodes on the snout tip). In addition, Curculionichthys sagarana can be diagnosed by the following characters: deeper caudal peduncle (8.4-9.6 % of SL, vs. 10.8-12.5% of SL in C. oliveirai; 10.2-11.3% in C. paresi); greater head length (34.8-40.5% of SL, vs. 28.8-33.3% of SL in C. luteofrenatus; 27.9-32.2% of SL in C. piracanjuba); shorter snout (46.3-52.4% of HL, vs. 67.0-75.3% of HL in C. luteofrenatus; 67.7-72.7% of HL in C. piracanjuba); shorter interorbital width (27.4-33.6% of SL, vs. 33.3-45.4% of HL in C. luteofrenatus; 36.7-40.9% of HL in C. piracanjuba; 33.8-37.8% of HL in C. coxipone); deeper head (41.2-49.1% of HL, vs. 51.6-59.2% of HL in C. oliveirai); shorter dorsal-spine (19.9-24.4% of SL, vs. 25.2-27.0% of SL in C. paresi); and shorter pectoral-spine (21.5-25.2% of SL, vs. 27.0-30.1% of SL in C. paresi) (Ref. 113800).

生物学     用語集 (例 epibenthic)

Life cycle and mating behavior 成熟 | 繁殖 | 放精 | | 生産力 | 幼生

主な参考文献 Upload your references | 参考文献 | コーディネーター : Fisch-Muller, Sonia | 協力者

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のレッドリストの状況は (Ref. 130435)

  軽度懸念 (LC) ; Date assessed: 13 November 2020

CITES

Not Evaluated

CMS (Ref. 116361)

Not Evaluated

人間に対する脅威

  Harmless





Human uses

FAO - Publication: search | FishSource |

より多くの情報

国々
国連食糧農業機関の区域
エコシステム
事件
導入
Stocks
生態学

食品種目概要について
摂食量
定量
共通名の
類義語
代謝
捕食動物
生態毒性
繁殖
成熟
放精
卵の集合体
生産力

卵の開発
Age/Size
成長
体長-重さ
Length-length
体長組成
形態計測学
形態学
幼生
幼生の動力
補充
豊度
BRUVS
参考文献
水産養殖
水産養殖の紹介
緊張
遺伝子の
Electrophoreses
遺伝
病気
行列
Nutrients
Mass conversion
協力者
画像
Stamps, Coins Misc.

シガテラ(食中毒の名前)
速度
泳ぐ 型式
カマ
Otoliths

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インターネットの情報源

AFORO (otoliths) | Aquatic Commons | BHL | Cloffa | BOLDSystems | Websites from users | Check FishWatcher | CISTI | Catalog of Fishes: 部類, | DiscoverLife | ECOTOX | FAO - Publication: search | Faunafri | Fishipedia | Fishtrace | GenBank: ゲノム, ヌクレオチド | GloBI | Google Books | Google Scholar | Google | IGFA World Record | MitoFish | Otolith Atlas of Taiwan Fishes | PubMed | Reef Life Survey | Socotra Atlas | 生命の木 | Wikipedia: 行く, 検索する | World Records Freshwater Fishing | Zoobank | 動物に関する記録

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).
栄養段階 (Ref. 69278):  2.6   ±0.1 se; based on size and trophs of closest relatives
回復力 (Ref. 120179):  高い, 15か月以下の倍増期間の最小個体群 (Preliminary K or Fecundity.).
Fishing Vulnerability (Ref. 59153):  Low vulnerability (10 of 100).