Orthochromis indermauri

Orthochromis indermauri Schedel, Vreven, Katemo Manda, Abwe, Chocha Manda & Schliewen, 2018

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Image of Orthochromis indermauri
No image available for this species;
drawing shows typical species in Cichlidae.

分類 / 名前 共通名の | 類義語 | Catalog of Fishes(部類, ) | ITIS | CoL | WoRMS | Cloffa

> Cichliformes (Cichlids, convict blennies) > Cichlidae (Cichlids) > Pseudocrenilabrinae
Etymology: Orthochromis: Greek, ortho = straight + Greek, chromis = a fish, perhaps a perch (Ref. 45335)indermauri: The species name indermauri honours the Swiss ichthyologist Dr. Adrian Indermaur, who was the first to document this new species with underwater photographs, videos, and with aquarium observations, thereby contributing to a large extent to our knowledge of behaviour and ecology of this species (Ref. 122085).
Eponymy: Dr Adrian Indermaur (d: 1984) is a Swiss ichthyologist who is (2014) Head of the animal facility at the Waler Salzburger Laboratory. [...] (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 底生の漂泳性; pH range: 8.0 - 8.6. Tropical; 23°C - 28°C (Ref. 122085)

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: lower reaches of Lufubu River, tributary of Lake Tanganyika, in Zambia (Ref. 122085).

サイズ / 重さ / 年齢

成熟: Lm ?  range ? - ? cm
Max length : 6.9 cm SL オス/雌雄の選別がない; (Ref. 122085)

簡単な記述 検索表 | 形態学 | 形態計測学

背面の脊椎 (合計) : 17 - 18; 背鰭 (合計) : 8 - 10; 肛門の骨: 3; 臀鰭: 7 - 9; 脊つい: 28 - 29. Diagnosis: Orthochromis indermauri is distinguished from all species currently placed in Orthochromis, except O. torrenticola, by having hypurals 1 and 2 clearly separated or separated by distinct seam vs. always fused (Ref. 122085). It is further distinguished from Malagarasi-Orthochromis species, except O. mazimeroensis, O. malagaraziensis, and O. rubrolabialis, by having fewer caudal vertebrae, 14-15 vs. 16-18, and total vertebrae, 28-29 vs. 30-32; it is also distinguished from O. luichensis, O. malagaraziensis, O. mazimeroensis, O. mosoensis by having more inner series of teeth in upper jaw, 3-5 vs. 1-2; moreover, it differs from O. kasuluensis by having fewer anal-fin rays, 7-9 vs. 10; from O. malagaraziensis by having more scales between upper lateral line and dorsal-fin origin, 5-7 vs. 3-4, and by having more ceratobranchial gill rakers, 8-11 vs. 6-7; from O. mazimeroensis by having more abdominal vertebrae, 14-15 vs. 12-13; from O. mosoensis and O. rubrolabialis by having more ceratobranchial gill rakers, 8-11 vs. 5-7, and total gill rakers, 11-15 vs. 8-10; from O. uvinzae by having fewer horizontal line scales, 25-29 vs. 30-32, fewer dorsal-fin spines, 17-18 vs. 19-20, and by position of pterygiophore supporting last dorsal-fin spine, vertebral count 16-17 vs. 18-19 (Ref. 122085). It is distinguished from O. kalungwishiensis, O. luongoensis, and O. torrenticola by having fewer horizontal line scales, 28-29 vs. 30-32, and by having fewer caudal vertebrae, 14-15 vs. 17-18; further, it differs from O. luongoensis and O. machadoi by having fewer series of scales on cheek, 0-1 vs. 2-5; from O. kalungwishiensis by having fewer total vertebrae, 28-29 vs. 31-33 (Ref. 122085). It is distinguished from Schwetzochromis neodon by having fewer horizontal line scales, 28-29 vs. 30-31, more circumpeduncular scales, 16 vs. 12, fewer caudal vertebrae, 14-15 vs. 16-17, fewer total vertebrae, 28-29 vs. 30-32, fewer dorsal-fin rays, 8-10 vs. 11-12, and by having hypurals 1 and 2 clearly separated or separated by distinct seam vs. fused; it differs from Haplochromis snoeksi by having fewer scales on cheek, 0-1 vs. 2-3, fewer horizontal line scales, 25-29 vs. 30-31, more abdominal vertebrae, 14-15 vs. 13, fewer caudal vertebrae, 14-15 vs. 17, fewer total vertebrae, 28-29 vs. 30, more anal-fin rays, 7-9 vs. 5-6, more dorsal-fin spines, 17-18 vs. 16, more ceratobranchial gill rakers, 8-11 vs. 6, and total gill rakers, 11-15 vs. 9; from Haplochromis bakongo by having more inner series of teeth, 3-5 vs. 1-2, more dorsal-fin spines, 17-18 vs. 14-15, and in position of pterygiophore supporting last dorsal-fin spine, vertebral count 16-18 vs. 13-14; from Haplochromis moeruensis by having hypurals 1 and 2 clearly separated or separated by distinct seam vs. always fused; meristic values of O. indermauri overlap with those of Haplochromis vanheusdeni but is distinguished in head mask, nostril stripe present vs. absent, caudal corner of cheek with blackish element vs. no such element present, and by size and colouration of eggspot-like maculae on anal fin, deep red centre vs. orange centre in Haplochromis vanheusdeni (Ref. 122085). It is distinguished from O. mporokoso and O. katumbii by having fewer caudal vertebrae, 14-15 vs. 16-17, fewer total vertebrae, 28-29 vs. 30-31, and by having hypurals 1 and 2 and hypurals 3 and 4 clearly separated or separated by distinct seam vs. always fused; further from O. mporokoso by having fewer series of scales on cheek, 0-1 vs. 2-4; from O. katumbii by having fewer horizontal line scales, 25-29 vs. 30-31; it is distinguished from O. kimpala by having fewer series of scales on cheek, 0-1 vs. 3-4, and by having more dorsal-fin spines, 17-18 vs. 15-16; meristic values of O. indermauri overlap with those of O. gecki but is distinguished by having a wider interorbital width, 13.5-18.2% of head length vs. 9.6-12.9% (Ref. 122085).
Body shape (shape guide): fusiform / normal.

生物学     用語集 (例 epibenthic)

Found in part of river which is rocky with some patches of sand and gravel, about 20 meters wide and on average 50 cm deep (Ref. 122085). This species is benthic-rheophilic and prefers stretches of fast flowing water where it is found between and among large rocks or patches of gravel (Ref. 122085). It is a maternal mouthbrooder (Ref. 122085).

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 : Kullander, Sven O. | 協力者

Schedel, F.D.B., E.J.W.M.N. Vreven, B. Katemo Manda, E. Abwe, A. Chocha Manda and U.K. Schliewen, 2018. Description of five new rheophilic Orthochromis species (Teleostei: Cichlidae) from the Upper Congo drainage in Zambia and the Democratic Republic of the Congo. Zootaxa 4461(3):301-349. (Ref. 122085)

IUCNのレッドリストの状況は (Ref. 130435: Version 2025-2 (Global))


CITES

Not Evaluated

CMS (Ref. 116361)

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
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
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参考文献
参考文献

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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=0.00389 (0.00180 - 0.00842), b=3.12 (2.94 - 3.30), in cm total length, based on all LWR estimates for this body shape (Ref. 93245).
0
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 (11 of 100). 🛈