分类 / Names
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Myxini
盲鳗纲 (丑鱼) (hagfishes) >
Myxiniformes (Hagfishes) >
Myxinidae (Hagfishes) > Eptatretinae
Etymology: Eptatretus: hepta (Gr.), seven; tretos (Gr.), perforated (i.e., with holes), referring to seven gill apertures on what would later be described as Homea banksii (=E. cirrhatus) [range within genus is 6-14 pairs of gill apertures]. (See ETYFish); luzonicus: -icus (Gr.), belonging to: Luzon Island, Philippines, type locality [replacement name of E. fernholmi McMillan & Wisner 2004, which became a junior homonym of Paramyxine fernholmi Kuo, Huang & Mok 1994 when Paramyxine was subsumed into Eptatretus]. (See ETYFish).
Environment: milieu / climate zone / depth range / distribution range
生态学
海洋 深海底的; 非迁移的; 深度上下限 563 - 710 m (Ref. 95645). 深水域; 7°C - ? (Ref. 95645); 20°N - 5°N, 116°E - 128°E
Western Pacific: known only from the type locality in the Philippines.
西太平洋: 在菲律賓已知只來自模式標本產地了。
大小 / 重量 / 年龄
Maturity: Lm ?  range ? - ? cm
Max length : 37.3 cm TL 雄鱼/尚未辨别雌雄; (Ref. 95645); 56.3 cm TL (female)
简单描述
型态特徵 | 形态测量图
This species can be distinguished from its known congeners by the following set of characters: gill pouches 8 pairs; 3-cusp multicusps on the anterior sets and 2-cusp multicusps on the posterior sets of cusps; total cusps 47-51; prebranchial pores 13-15; trunk pores 49-55; total pores 84-88; a single nasal-sinus papilla in the middorsal surface of the nasal sinus (Ref. 95645).
鳃囊与孔 8. 融合的尖头 3/2 ,总尖头 51. 总黏液孔 81. 眼斑不存在。 腹面鳍褶退化的.(参考文献 51420)
The holotype was collected from the type locality over green muddy bottom at bottom temperature of 6.8°C, surface water temperature 28.3°C (Anonymous, 1910). Additional specimens from the Verde Island Passage were collected at 578 and 710 m, sediment type ranged from mud to sand (Ref. 95645).
Life cycle and mating behavior
成熟度 | 繁殖 | 产卵场 | 卵 | 孕卵数 | 仔鱼
西太平洋: 在菲律賓已知只來自模式標本產地了。
Mincarone, M.M. and J.E. McCosker, 2014. Redescription of Eptatretus luzonicus Fernholm et al., 2013, a replacement name for Eptratretus fernholmi McMillan and Wisner, 2004 (Craniata: Myxinidae), based on the discovery of the holotype and additional specimens from the Philippines. pp. 341-349. In Williams, G.C. and T.M. Gosliner, eds. 2014. The Coral Triangle : The 2011 Hearst Biodiverisity Philippine Expedition. California Academy of Sciences, San Francisco, California 94118, USA. (Ref. 95645)
人类利用
更多信息
俗名同种异名新陈代谢捕食者生态毒物学繁殖成熟度产卵场产卵群集孕卵数卵卵的发育
年龄范围成长体长-体重体长-体长体长-频率形态测量图型态特徵仔鱼稚鱼动力学入添量丰度BRUVS
参考文献养殖养殖信息品种遗传学Electrophoreses遗传率疾病加工NutrientsMass conversion
合作者照片Stamps, Coins Misc.声音神经毒速度泳型鳃区Otoliths脑重体重比眼睛色素
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Estimates based on models
Phylogenetic diversity index (Ref.
82804): PD
50 = 0.5000 [Uniqueness, from 0.5 = low to 2.0 = high].
Bayesian length-weight: a=0.00204 (0.00092 - 0.00452), b=2.93 (2.73 - 3.13), in cm total length, based on LWR estimates for this (Sub)family-body shape (Ref.
93245).
营养阶层 (Ref.
69278): 4.2 ±0.7 se; based on size and trophs of closest relatives
回复力 (Ref.
120179): 低的, 最小族群倍增时间4.5 - 14 年 (Fec assumed to be <100).
Fishing Vulnerability (Ref.
59153): Moderate vulnerability (43 of 100).