Steganoderma Stafford, 1904(狄亚纲:虫纲:鳞蝗科)俄勒冈深海两种岩鱼的记述,包括一新种和该属物种检索表的更新

C. K. Blend, Gábor R. Rácz
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引用次数: 1

摘要

描述了从1859年绿条纹岩鱼(sebases elongatus Ayres)和旗纹岩鱼(sebases rubrivinctus) (Jordan and Gilbert, 1880年)(Scorpaeniformes: Sebastidae)的肠道中采集的美国俄勒冈州190-200 m深度的Steganoderma eamiqtrema n. p.)和1904年的单一未识别的Stafford Steganoderma Stafford标本(动物虫科:鳞片虫科)。该新种与其他7个同属物种的区别在于其形态特征的诊断组合,包括一个细长的卵形到纺锤形的身体,一个位于前体和后体的棍棒状到逗号形的卷云袋,一个分两部分的精囊,一个分两部分的生殖孔,一个比口腔更大的腹侧吸盘,以及一个光滑的睾丸和卵巢,它们之间的距离相对较小。我们提出了一个更新的密钥,目前在Steganoderma 8种,并提供了一份已知的寄生虫清单。长丝和丝。rubrivinctus。s.e eamiqtrema的发现。长形虫是该寄主中已知的第二种动物类人猿,而Steganoderma sp.在Se的发现。Rubrivinctus是该寄主物种中首次报道的地沟虫。本文还对模式种S. formosum Stafford, 1904进行了详细的讨论,并提出了关于该物种是否具有世界性分布并感染如此广泛的鱼类宿主的问题。我们提出了证据,包括我们在模式种的重新描述中观察到的变异,质疑在如此漫长的地质时期内,北大西洋和北太平洋地理上分开的同种蠕虫之间可能存在基因流动的不可信的想法,并提出一些先前报道的S. formosum可能确实是S. eamiqtrema的可能性;所有这些都表明,台湾猕猴可能是一个物种复合体的一部分,而不是同一个世界物种。在深海中,以S. eamiqtrema、S. formosum和Steganoderma sp.为代表的是Steganoderma,关于该属的寄主特异性和新物种在深水中的生活史策略的推测有限。最后,我们迫切需要对Steganoderma的物种进行分子研究(即,目前在GenBank中没有该属任何物种的DNA序列数据),我们怀疑通过进一步的分子,形态学和生活史研究,该属将被分类划分。
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Steganoderma Stafford, 1904 (Digenea: Zoogonidae: Lepidophyllinae) from Two Species of Rockfishes from Deep Waters off Oregon Including a New Species and an Updated Key to Species of This Genus
Steganoderma eamiqtrema n. sp. and a single unidentified specimen of Steganoderma Stafford, 1904 (Zoogonidae: Lepidophyllinae) obtained from the intestine of the greenstriped rockfish, Sebastes elongatus Ayres, 1859, and the flag rockfish, Sebastes rubrivinctus (Jordan and Gilbert, 1880) (Scorpaeniformes: Sebastidae), collected from 190–200 m depths off Oregon, USA, are described. The new species is distinguished from its seven other congeners by a diagnostic combination of morphological features including an elongate oval to spindle-shaped body, a clavate to comma-shaped cirrus pouch located in the forebody and hindbody, a bipartite seminal vesicle, a bifurcal or just post-bifurcal genital pore, a larger ventral than oral sucker, and a smooth testes and ovary with a relatively small distance between them. We present an updated key to the eight species now in Steganoderma and provide a list of parasites known from Se. elongatus and Se. rubrivinctus. The discovery of S. eamiqtrema in Se. elongatus represents the second species of zoogonid known from this host, and the finding of Steganoderma sp. in Se. rubrivinctus represents the first report of a digenean from this host species. A detailed discussion also is given of the type species, S. formosum Stafford, 1904, and questions are raised as to whether this species has a worldwide distribution and infects such a wide variety of fish hosts. We present evidence including variation we observed in redescriptions of the type species, query the implausible idea that there could be gene flow between conspecific helminths geographically separated in the North Atlantic and North Pacific Oceans over such a vast geological period, and offer the possibility that some prior reports of S. formosum may, indeed, be S. eamiqtrema; all of which suggests S. formosum sensu lato may be part of a species complex and not the same worldwide species. Steganoderma is represented in the deep sea by S. eamiqtrema, S. formosum, and Steganoderma sp., and limited speculation is given as to the host specificity of this genus and life history strategies of the new species in deeper waters. Finally, molecular studies of species of Steganoderma are sorely needed (i.e., there is no DNA sequence data currently available in GenBank for any species of this genus), and we suspect that with further molecular, morphological, and life history work, this genus will be taxonomically divided up.
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