Curculionichthys sabaji

Curculionichthys sabaji Roxo, Silva, Ochoa & Oliveira, 2015

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Image of Curculionichthys sabaji
No image available for this species;
drawing shows typical species in Loricariidae.

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

> Siluriformes (Catfishes) > Loricariidae (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 genussabaji: Named for Dr. Mark Henry Sabaj Pérez, Collection Manager of Ichthyology, Academy of Natural Sciences of Philadelphia, in recognition of his dedication and contributions to study of Neotropical fishes especially from Rio Xingu basin (iXingu Project).
Eponymy: Dr Mark Henry Sabaj Pérez (d: 1969) is an ichthyologist and collection manager of fishes at the Academy of Natural Sciences of Philadelphia (2000–present). [...] (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

South America: Rio Xingu basin in Brazil.

サイズ / 重さ / 年齢

成熟: Lm ?  range ? - ? cm
Max length : 2.4 cm SL オス/雌雄の選別がない; (Ref. 113800)

簡単な記述 検索表 | 形態学 | 形態計測学

背鰭 (合計) : 9; 臀鰭: 5; 脊つい: 28. Curculionichthys sabaji is distinguished from all congeners by possessing several dark-brown spots distributed on the body (vs. a variety of pigment patterns, but none of which includes dark-brown spots). It also differs from all con¬geners, except C. coxipone and C. paresi by having the cleithrum with an area free of odontodes (vs. cleithrum completely covered with odontodes). Other characters useful to further diagnosed this species from other congengers include the following: some papillae of the lower lip arranged in a medial longitudinal series extending posterior to dentaries through the middle portion of the lower lip (vs. lower lip with all papillae randomly distributed in from C. piracanjuba, C. sagarana, and C. oliveirai); anterior profile of the head pointed (vs. rounded in C. coxipone and C. oliveirai); odontodes forming longitudinally aligned rows on head and trunk (vs. odontodes not forming longitudinally aligned rows on head and trunk in C. piracanjuba); small, inconspicuous odontodes forming rows on the head and trunk (vs. large, conspicuous odontodes forming rows on the head and the trunk in C. insperatus); caudal fin hyaline, with one dark strip extending from caudal peduncle base to the median caudal fin rays, and dark chromatophores irregular distributed almost forming two bands (vs. caudal fin hyaline, with dark blotch limited to caudal peduncle base in C. insperatus and C. sagarana); absence of one unpaired platelet on the dorsal portion of caudal peduncle (vs. one unpaired platelet on the dorsal portion of the caudal peduncle in C. sagarana); 6?9 lateral abdomen plates (vs. 4?5 lateral abdomen plates in C. oliveirai); absence of contrasting dark geometric spots on the anterodorsal region of body (vs. pres¬ence of geometric spots in C. paresi); not having hypertrophied odontodes on the snout tip (vs. hypertrophied odontodes on the snout tip in C. piracanjuba). In addition, Curculionichthys sabaji can be distinguished by having a shorter dorsal fin spine (18.5?22.7% of SL, vs. 25.2?27.0% of SL in C. paresi; 23.2?26.9% of SL in C. insperatus); a shorter pectoral-fin spine (18.9?23.4% of SL, vs. 27.0?30.1% of SL in C. paresi); a deeper caudal peduncle (7.0?10.0% of SL, vs. 10.8?12.5% of SL in C. oliveirai; 10.2?11.3% of SL in C. paresi); a deeper head (40.9?49.1% of HL, vs. 51.6?59.2% of HL in C. oliveirai); a longer head (34.3?38.6% of SL, vs. 27.9?32.2% of SL in C. piracanjuba; 28.8?33.3% of SL in C. luteofrenatus); a shorter snout (45.5?56.9% of HL, vs. 67.7?72.7% of HL in C. piracanjuba; 67.0?75.3% of HL in C. luteofrenatus) and a shorter interorbital width (30.3?35.7% of HL, vs. 36.7?40.9% of HL in C. piracanjuba; 67.0?75.3% of HL in C. luteofrenatus) (Ref. 113800).
Body shape (shape guide): elongated.

生物学     用語集 (例 epibenthic)

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 : Fisch-Muller, Sonia | 協力者

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

水産業: 興味がない
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
類義語
形態学
形態計測学
画像
参考文献
参考文献

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インターネットの情報源

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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 = 0.5001 [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).
栄養段階
(参照 69278)
2.7   ±0.1 se; based on size and trophs of closest relatives
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 (10 of 100). 🛈