Marcusenius devosi Kramer, Skelton, van der Bank & Wink, 2007
分類 / 名前 共通名の | 類義語 | Catalog of Fishes(部類, 種) | ITIS | CoL | WoRMS | Cloffa
> Osteoglossiformes (Bony tongues) > Mormyridae (Elephantfishes)
Etymology: Marcusenius: Becasue of J. Marcusen, author of "Zur Phauna des Schwarzen Meeres", 1867; ichthyologist; devosi: Marcusenius devosi is named in honour of Dr. Luc De Vos, late curator of fishes at Nairobi Museum, for his contributions to African ichthyology and promotion of ichthyology in East Africa (Ref. 75962).
Eponymy: Dr Johann Andreas Marcusen (1817–1894) was a Latvian of German descent who was a physician, ichthyologist and zoologist. [...] Dr Luc De Vos (1957–2003) was a Belgian ichthyologist who was Curator of Fishes at the Nairobi Museum, Kenya. [...] (Ref. 128868), visit book page.
Etymology: Marcusenius: Becasue of J. Marcusen, author of "Zur Phauna des Schwarzen Meeres", 1867; ichthyologist; devosi: Marcusenius devosi is named in honour of Dr. Luc De Vos, late curator of fishes at Nairobi Museum, for his contributions to African ichthyology and promotion of ichthyology in East Africa (Ref. 75962).
Eponymy: Dr Johann Andreas Marcusen (1817–1894) was a Latvian of German descent who was a physician, ichthyologist and zoologist. [...] Dr Luc De Vos (1957–2003) was a Belgian ichthyologist who was Curator of Fishes at the Nairobi Museum, Kenya. [...] (Ref. 128868), visit book page.
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
Africa: Tana River, but range extension both to the north and south likely (Ref. 75962).
サイズ / 重さ / 年齢
簡単な記述 検索表 | 形態学 | 形態計測学
背面の脊椎 (合計) : 0; 背鰭 (合計) : 21 - 24; 肛門の骨: 0; 臀鰭: 26 - 30. Diagnosis: Marcusenius devosi can be distinguished from its congeners by the following characters: distance dorsal fin origin to end of caudal peduncle 39.5-43.4% of standard length, preanal distance 57.0-61.0% of standard length, predorsal distance 59.8-64.0% of standard length, caudal peduncle length 19.2-22.1% of standard length, number of scales in linear series along the lateral line row 56-66, dorsal fin rays 21-24, anal fin rays 26-30, and 14-18 scales around caudal peduncle (Ref. 75962). Electric organ discharge lacking weak head-negative pre-potential, strong Namp relative to Pamp, but short Ndur, Pdur of long duration (Ref. 75962).
description: Head with terminal mouth well in front of eye, mental lobe on lower jaw protruding beyond upper jaw; head and body dorsolaterally compressed (Ref. 75962). Dorsal fin situated about two thirds of standard length from snout, obliquely orientated, anteriorly higher and posteriorly lower, distal margin sometimes only slightly crescentic with anterior two or three rays longer than posterior rays, number of rays 21-24; anal fin opposite dorsal fin with distinctly more anterior origin, obliquely orientated, anteriorly lower and posteriorly higher, anterior rays longer than posterior ones, especially in males where they also appear stronger and often darkened, distal margin crescentic, number of rays 26-30 (Ref. 75962). Scales cycloid with reticulate striae, scales extending anteriorly to operculum and pectoral fins; scales on caudal peduncle circumference, 14-18 (Ref. 75962). Caudal peduncle relatively deep, subcylindrical enire length, usually 19.0-21.0 on standard length (Ref. 75962). Electric organ discharge biphasic lacking a weak pre-potential, Pamp of relatively long duration, increasing with standard length at least in females and juveniles, Ndur of very short duration, but very strong Namp; no sexual dimorphism recognized (Ref. 75962).
Colouration: Colour in preservation: head and back when seen from above, dark; body sides light brown to light ochre, the ochre found especially on lower parts and underside; dorsal fin usually darker than anal fin; homogeneous colouration without any blotches, increasingly lighter from back to belly (Ref. 75962).
Body shape (shape guide): fusiform / normal; Cross section: compressed.
Body shape (shape guide): fusiform / normal; Cross section: compressed.
ライフサイクルと交尾行動 成熟 | 繁殖 | 放精 | 卵 | 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 | 協力者
Kramer, B., P. Skelton, H. van der Bank and M. Wink, 2007. Allopatric differentiation in the Marcusenius macrolepidotus species complex in southern and eastern Africa: the resurrection of M. pongolensis and M. angolensis, and the description of two new species (Mormyridae, Teleostei). J. Nat. Hist. 41(9-12):647-708. (Ref. 75962)
IUCNのレッドリストの状況は (Ref. 130435: Version 2025-2 (Global))
絶滅危惧に近い (NT) (B1ab(i,ii,iii)); Date assessed: 29 June 2022
CITES
Not Evaluated
人間に対する脅威
Harmless
人間の用途
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
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
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
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
卵の開発
幼生
幼生の動力
繁殖
成熟
成熟度／エラ
生産力
放精
産卵群
卵
卵の開発
幼生
幼生の動力
解剖学
カマ
脳
オトリス
カマ
脳
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）
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
ゲノム
遺伝子の
ヘテロ接合性
遺伝
遺伝的多様性
用具
特記事項
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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, 種 | 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 = 0.5000 [Uniqueness, from 0.5 = low to 2.0 = high]. |
| Bayesian length-weight | a=0.00562 (0.00248 - 0.01273), b=3.05 (2.85 - 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) |
3.2 ±0.4 se; based on size and trophs of closest relatives |
|
回復力 (参照 120179) |
非常に低い, １４年以上の倍増期間の最小個体群 (Preliminary K or Fecundity.). |
|
漁業の脆弱性 (Ref. 59153) |
High to very high vulnerability (71 of 100). 🛈 |