Heptapterus carmelitanorum Deprá, Aguilera, Faustino-Fuster, Katz & Azevedo-Santos, 2022
Carmelitano catfish
分類 / 名稱 俗名 | 同種異名 | Catalog of Fishes(屬, 種) | ITIS | CoL | WoRMS | Cloffa
Teleostei > Siluriformes (Catfishes) 鯰形目 (Catfishes) > Heptapteridae (Three-barbeled catfishes) 七鰭鯰科 (Three-barbeled catfishes)
Etymology: Heptapterus: Greek, epta = seven + Greek, pteron = wing, fin (Ref. 45335); carmelitanorum: Name from Carmelitanos (Portuguese), the local appellation of people born or living in Carmo do Rio Claro, Minas Gerais, Brazil (where the species was discovered) and especially in honor of Ana Maria Vilela Soares, José Cândido de Mello Carvalho, Moara Lemos, and Carlos Roberto Bueno Júnior, for their contributions to biological science: noun in apposition.
Etymology: Heptapterus: Greek, epta = seven + Greek, pteron = wing, fin (Ref. 45335); carmelitanorum: Name from Carmelitanos (Portuguese), the local appellation of people born or living in Carmo do Rio Claro, Minas Gerais, Brazil (where the species was discovered) and especially in honor of Ana Maria Vilela Soares, José Cândido de Mello Carvalho, Moara Lemos, and Carlos Roberto Bueno Júnior, for their contributions to biological science: noun in apposition.
環境： 環境 / 氣候帶 / 深度上下限 / 配送範圍 生態學
海洋 居於水底的; 深度上下限 0 - 1 m (Ref. 127242).
分布 領土 | FAO區域 | 生態系 | 發現紀錄 | 分布圖 | 簡介 | Faunafri
South America: Brazil.
大小 / 重量 / 年齡
簡短描述 檢索表 | 型態特徵 | 形態測量圖
This species is distinguished from its congeners by the following characters: anal-fin insertion less than one eye diameter posterior to a vertical through the adipose-fin insertion (vs. more than one eye diameter posterior); differs from all congeners, except H. borodini, by having an isognathous mouth (vs. slightly to moderately retrognathous); differs from all congeners except H. borodini and H. hollandi, by the keel formed by ventral procurrent caudal-fin rays shallow, far from reaching anal-fin base (vs. keel formed by ventral procurrent caudal-fin rays deep, continuing almost to the anal-fin base, even though its anterior part is devoid of fin rays); differs from H. borodini and H. hollandi by having an almost elliptical caudal fin (vs. lanceolate in H. borodini, obliquely truncate to falcate in H. hollandi; length of its dorsal lobe 18.3-19.3% SL (vs. 24.4-43.3% SL in H. borodini); differs from congeners, except carnatus, mbya, qenqo, and some specimens of H. hollandi, by having inconspicuous dorsal bars (vs. conspicuous); differs borodini, carnatus, exilis, hollandi, mustelinus, ornaticeps, by having 14-15 anal-fin rays (vs. 10-12 in borodini, hollandi; 18-21 in H. carnatus; 16-19 in H. exilis; 18-23 in H. mustelinus; and 19 in H. ornaticeps); differs from H. exilis by having a complete lateral line (in adults), continuous to base of hypural plate (vs. incomplete, not reaching dorsal-fin insertion); differs further from H. hollandi by having i,6 dorsal-fin rays (vs. i,7) (Ref. 127242).
Cross section: oval.
Cross section: oval.
Collection area with the water extremely clear (small characids readily observed) and
well oxygenated. The stream was shallow (not exceeding 1 meter), and its bed was completely formed by rocks; light penetration was low during samplings. the reach, submerged tree roots and accumulated leaves and fruits (especially Fabaceae) formed some microhabitats for some species, notably Trichomycterus candidus and Cetopsorhamdia iheringi, Specimens of this species were captured in environments that combined rocks (generally juxtaposed) and a more turbulent flow. The species is apparently demersal upon observation sampling. The species was collected with C. iheringi, Hoplias malabaricus, Knodus moenkhausii, Odontostilbe weitzmani, Oligosarcus argenteus, Pareiorhina sp., Psalidodon sp., T. candidus, T. septemradiatus (Ref.
生命週期和交配行為 成熟度 | 繁殖 | 產卵場 | 卵 | 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 : Bockmann, Flavio | 合作者
Deprá, G. de Carvalho, G. Aguilera, D.R. Faustino-Fuster, A.M. Katz and V.M. Azevedo-Santos, 2022. Redefinition of Heptapterus (Heptapteridae) and description of Heptapterus carmelitanorum, a new species from the upper Paraná River basin in Brazil. Zoosyst. Evol. 98(2):327-343. (Ref. 127242)
CITES
Not Evaluated
對人類具威脅
人類使用
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
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
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
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
解剖學
鰓區
腦部
耳石
鰓區
腦部
耳石
生理學
身體成分
營養素
耗氧量
游泳類型
游泳速度
視覺色素
魚聲
疾病與寄生蟲
毒性 (LC50s)
身體成分
營養素
耗氧量
游泳類型
游泳速度
視覺色素
魚聲
疾病與寄生蟲
毒性 (LC50s)
遺傳學
基因組
遺傳學
異種性
遺傳率
遺傳多樣性
基因組
遺傳學
異種性
遺傳率
遺傳多樣性
工具
特別的報告
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網路資源
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基於模型的估計
系統發育多樣性指數 (參考文獻 82804): PD50 = 0.5002 [Uniqueness, from 0.5 = low to 2.0 = high].
Bayesian length-weight: a=0.00813 (0.00379 - 0.01743), b=2.97 (2.79 - 3.15), 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): 3.5 ±0.4 se; based on size and trophs of closest relatives
回復力 (參考文獻 120179): 低的, 最小族群倍增時間4.5 - 14 年 (Preliminary K or Fecundity.).