Curculionichthys sagarana

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Curculionichthys sagarana Roxo, Silva, Ochoa & Oliveira, 2015

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

分類 / 名前 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 genussagarana: 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.

環境:環境 / 気候帯 / 深さの範囲 / 分布範囲 生態学

; 新鮮な水 底生の. Tropical

分布 領土 | 国連食糧農業機関の区域 | エコシステム | 事件 | 目的のマップ | 導入 | Faunafri

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

サイズ / 重さ / 年齢

成熟: 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 検索表 | 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).
Body shape (shape guide): elongated.

生物学     用語集 (例 epibenthic)

ライフサイクルと交尾行動 成熟 | 繁殖 | 放精 | | 生産力 | 幼生

主な参考文献 参考文献のアップロード | 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: Version 2025-2 (Global))

  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





人間の用途

水産業: 興味がない
FAO - Publication: search | FishSource |

より多くの情報

養殖生態
食料品(獲物)
餌の構成
摂食量
食料配給
捕食動物
生態学
生態学
人口動態
成長のパラメーター
最大年齢/サイズ
長さ-重量比。
長短関係。
体長組成
質量変換
補充
豊度
ライフサイクル
繁殖
成熟
成熟度/エラ
生産力
放精
産卵群

卵の開発
幼生
幼生の動力
分布
領土
国連食糧農業機関の区域
エコシステム
事件
導入
BRUVS - ビデオ
解剖学
カマ

オトリス
生理学
体組成
栄養素
酸素消費
水泳タイプ
泳ぐ速さ
視覚色素
フィッシュ・サウンド
病気と寄生虫
毒性(LC50)
遺伝子の
ゲノム
遺伝子の
ヘテロ接合性
遺伝
遺伝的多様性
人間関係
養殖システム
水産養殖の紹介
緊張
シガテラ症例
切手、コイン、その他
アウトリーチ
協力者
分類学
共通名の
類義語
形態学
形態計測学
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参考文献
参考文献

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インターネットの情報源

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

モデルに基づく推定値

系統多様性指数 (参照 82804):  PD50 = 0.5001   [Uniqueness, from 0.5 = low to 2.0 = high].
Bayesian length-weight: a=0.00977 (0.00434 - 0.02202), b=3.06 (2.87 - 3.25), in cm total length, based on LWR estimates for this (Sub)family-body shape (Ref. 93245).
栄養段階 (参照 69278):  2.6   ±0.1 se; based on size and trophs of closest relatives
回復力 (参照 120179):  高い, 15か月以下の倍増期間の最小個体群 (Preliminary K or Fecundity.).
漁業の脆弱性 (Ref. 59153):  Low vulnerability (10 of 100). 🛈