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Haplochromis squamipinnis
Female 画像によって Schraml, E.
画像 | グーグルの画像
Female 画像によって Schraml, E.
分類 / 名前 共通名の | 類義語 | Catalog of Fishes(部類, 種) | ITIS | CoL | WoRMS | Cloffa
> Cichliformes (Cichlids, convict blennies) > Cichlidae (Cichlids) > Pseudocrenilabrinae
Etymology: Haplochromis: Greek, Haploos = single + Greek, chromis = a fish, perhaps a perch (Ref. 45335); squamipinnis: Specific name not explained in original description, from the Latin 'squamus' for 'scale', and 'pinnis' for 'fin'; probably referring to minute scales on basal parts of dorsal and anal fins (Ref. 126312).
More on author: Regan.
Etymology: Haplochromis: Greek, Haploos = single + Greek, chromis = a fish, perhaps a perch (Ref. 45335); squamipinnis: Specific name not explained in original description, from the Latin 'squamus' for 'scale', and 'pinnis' for 'fin'; probably referring to minute scales on basal parts of dorsal and anal fins (Ref. 126312).
More on author: Regan.
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; 移住性ではない. Tropical; 1°N - 1°S
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: Lake Edward system, including Lake Edward, Kazinga Channel and Lake George (Ref. 126312). Introduced into Lake Kachira, Lake Victoria drainage, Uganda (Ref. 126312).
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) : 15 - 16; 背鰭 (合計) : 8 - 10; 肛門の骨: 3; 臀鰭: 9 - 11; 脊つい: 29 - 30. Diagnosis: Species with a piscivorous morphology; body rather deep, body depth 32.4-39.3% of standard length; oral jaws very long, lower jaw length 47.8-58.6% of head length, narrow, lower jaw width 32.6-44.7% of lower jaw length, and steep, gape inclination 30-45°; outer oral teeth many and small, 39-79; dominant males slate blue (Ref. 126312). Amongst piscivorous species from the Lake Edward system, Haplochromis squamipinnis differs from all by presence vs. absence of minute scales on proximal part of dorsal fin, rarely few scales present in H. quasimodo (Ref. 126312). It further differs from H. latifrons and H. mentatus by the combination of small vs. large outer oral teeth, a larger number of outer uppr jaw teeth, 39-79 vs. 22-47; a steeper gape, 30-45° vs. 15-30°; and a deeper body, body depth 32.4-39.3% of standard length vs. 27.2-32.3%; from H. mentatus by dominant males uniformly slate blue vs. yellow-green with a red anterior part of flank (Ref. 126312). It further differs from H. rex, H. simba, H. glaucus and H. aquila by the combination of small vs. large outer oral teeth, a larger number of outer upper jaw teeth, 39-79 vs. 22-47; and dominant males uniformly slate blue vs. cream-coloured with an orange operculum, yellow with an orange anterior part of flank, light blue with a dusky to black head, or light grey with a black head, respectively; further from H. rex, H. simba and H. glaucus by a steeper gape, 30-45° vs. 15-30°; further from H. aquila by a smaller eye, eye diameter 23.1-29.7% of head length vs. 30.0-31.5% (Ref. 126312). It further differs from H. kimondo by a concave to straight vs. convex dorsal outline of head, a gentler snout inclination, 30-40° vs. 40-50°, and dominant males slate blue vs. grey dorsally and yellow ventrally; further from H. falcatus by a shorter head, head length 35.1-36.9% of standard length vs. 36.6-39.6%, and dominant males slate blue vs. olve-green with an orange-red anterior part of flank; further from H. curvidens and H. pardus by a deeper cheek, cheek depth 24.9-36.0% of head length vs. 20.8-24.9%; further from H. pardus by a larger adult size, maximum size 211 mm standard length vs. 96 mm, and colour pattern of small specimens less than 100 mm standard length light coloured vs. speckled to uniformly black (Ref. 126312). It differs from H. quasimodo by the combination of a broader interorbital area, interorbital width 48.6-55.6% of head width vs. 40.5-48.7%; a longer lower jaw, lower jaw length 47.8-58.6% of head length vs. 44.2-49.6%; a steeper gape inclination, 30-45° vs. 20-35°; and dominant males slate blue vs. light grey dorsally and blue-black ventrally (Ref. 126312).
Found in offshore benthic areas in mostly shallow and deep waters over muddy substrates (Ref. 4983, 126312). With a piscivorous diet (Ref. 558, 126312); insects contribute substantially to the diet of small Haplochromis squamipinnis (Ref. 558).
ライフサイクルと交尾行動 成熟 | 繁殖 | 放精 | 卵 | 生産力 | 幼生
Mouthbrooding by females.
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
van Oijen, M.J.P., J. Snoeks, P.H. Skelton, C. Maréchal and G.G. Teugels, 1991. Haplochromis. p. 100-184. In J. Daget, J.-P. Gosse, G.G. Teugels and D.F.E. Thys van den Audenaerde (eds.) Check-list of the freshwater fishes of Africa (CLOFFA). ISNB, Brussels; MRAC, Tervuren; and ORSTOM, Paris. Vol. 4. (Ref. 4983)
CITES
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 |
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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=0.01445 (0.00671 - 0.03113), b=2.99 (2.82 - 3.16), 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 ±0.40 se; based on food items. |
|
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.). |
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漁業の脆弱性 (Ref. 59153) |
Low to moderate vulnerability (28 of 100). 🛈 |