Curculionichthys sagarana

Curculionichthys sagarana Roxo, Silva, Ochoa & Oliveira, 2015

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drawing shows typical species in Loricariidae.

分類 / 名稱 俗名 | 同種異名 | Catalog of Fishes(, ) | ITIS | CoL | WoRMS | Cloffa

Teleostei > Siluriformes (Catfishes) 鯰形目 (Catfishes) > Loricariidae (Armored catfishes) 甲鯰科 (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 / 氣候帶 / 深度上下限 / 配送範圍 生態學

; 淡水 居於水底的.

分布 領土 | FAO區域 | 生態系 | 發現紀錄 | 分布圖 | 簡介 | Faunafri

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

大小 / 重量 / 年齡

成熟度: Lm ?  range ? - ? cm
Max length : 2.3 cm SL 雄魚/尚未辨別雌雄; (Ref. 113800); 2.4 cm SL (female)

簡短描述 檢索表 | 型態特徵 | 形態測量圖

背的軟條 (總數) : 9; 臀鰭軟條: 6; 脊椎骨: 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.

生物學特性     字彙 (例如 epibenthic)


生命週期和交配行為 成熟度 | 繁殖 | 產卵場 | | 孕卵數 | 仔魚


主要參考資料 上傳您的推薦信 | 參考文獻 | 合作者 : Fisch-Muller, Sonia | 合作者

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 瀕危狀態 (Ref. 130435: Version 2025-2 (Global))

  無危 (LC) ; Date assessed: 13 November 2020

CITES

Not Evaluated

CMS (Ref. 116361)

Not Evaluated

對人類具威脅

 





人類使用

漁業: 沒有興趣
FAO - Publication: search | FishSource |

更多資訊

營養生態學
食物項目(獵物)
食性組成
食物消耗量
食物配給
捕食者
生態學
生態學
人口動態
成長參數
最大年齡/尺寸
長度重量比
長度關係
長度-頻率
質量轉換
入添量
豐度
生命週期
繁殖
成熟度
成熟度/鰓部相對
孕卵數
產卵場
產卵聚集

卵發育
仔魚
稚魚動力學
分布
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解剖學
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身體成分
營養素
耗氧量
游泳類型
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視覺色素
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疾病與寄生蟲
毒性 (LC50s)
遺傳學
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參考文獻
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網路資源

AFORO (otoliths) | Aquatic Commons | BHL | Cloffa | Websites from users | 檢查 FishWatcher | CISTI | Catalog of Fishes: , | 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 | 樹狀分類階層 | Wikipedia: , 搜尋 | World Records Freshwater Fishing | Zoobank | 動物學的記錄

基於模型的估計

系統發育多樣性指數
(參考文獻 82804)
PD50 = 0.5001 [Uniqueness, from 0.5 = low to 2.0 = high].
Bayesian length-weight a=0.00977 (0.00436 - 0.02192), b=3.06 (2.87 - 3.25), in cm total length, based on LWR estimates for this (Sub)family-body shape (Ref. 93245).
營養階層
(參考文獻 69278)
2.6   ±0.1 se; based on size and trophs of closest relatives
回復力
(參考文獻 120179)
高度, 族群倍增時間少於 15個月 (Preliminary K or Fecundity.).
釣魚的脆弱性
(Ref. 59153)
Low vulnerability (10 of 100). 🛈