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首页> 外文期刊>Systematic Parasitology >Molecular systematics of the Holarctic Anoplocephaloides variabilis (Douthitt, 1915) complex, with the proposal of Microcephaloides n. g. (Cestoda: Anoplocephalidae).
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Molecular systematics of the Holarctic Anoplocephaloides variabilis (Douthitt, 1915) complex, with the proposal of Microcephaloides n. g. (Cestoda: Anoplocephalidae).

机译:拟南芥无头畸形的分子系统学(Douthitt,1915),有Microcephaloides n。的提议。 G。 (Cestoda:无头目科)。

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Phylograms based on mitochondrial cytochrome oxidase I gene sequences show that the Anoplocephaloides variabilis (Douthitt, 1915)-like cestodes (Cestoda: Anoplocephalidae) from voles (Microtus spp.) and Paranoplocephala krebsi Haukisalmi, Wickstrom, Hantula & Henttonen, 2001 from collared lemmings (Dicrostonyx spp.) comprise a monophyletic group within the anoplocephaline cestodes. The patterns of phylogenetic, biological and/or biogeographical distinction suggest six or seven species of A. variabilis-like cestodes, including P. krebsi. However, at this time we decline to describe them as a series of new species as no straightforward morphological differences were found between the A. variabilis-like cestodes. A new genus, Microcephaloides n. g., is proposed for the cestodes earlier assigned to A. variabilis, A. cf. variabilis, A. tenoramuraiae Genov & Georgiev, 1988 and P. krebsi. A redescription is provided for the type-species, M. variabilis n. comb., from pocket gophers (Geomys spp. and Thomomys spp.). In addition to Anoplocephaloides Baer, 1927 (sensu stricto) and Microcephaloides, Paranoplocephaloides Gulyaev, 1996, Flabelloskrjabinia Spasskii, 1951 and Leporidotaenia Genov, Murai, Georgiev & Harris, 1990 are considered valid genera among cestodes previously assigned to Anoplocephaloides (sensu Rausch, 1976). The host spectrum and present phylogenetic data suggest that Microcephaloides has been primarily associated with voles (Microtus spp.) and its basal lineage now occurs in M. guentheri (Danford & Alston) in Turkey. Although the distribution and current host of the basal lineage suggest a western Palaearctic origin, subsequent diversification has probably occurred in eastern Beringia, because most of the more derived lineages occur partly or exclusively in Alaska.
机译:根据线粒体细胞色素氧化酶I基因序列的谱图显示,田鼠(Microtus spp。)的类no虫(Cestoda:Anoplocephalidae)的虫(Cestoda:Anoplocephalidae)和and虫(Panonoplocephala krebsi Haukisalmi,Wickstrom,Hantula&Hentula&Hentula&Hentula&Hentula&Hentula&Hentula&Hentula 2001) Dicrostonyx spp。)在头颅脑内包含一个单系统的基团。系统发育,生物学和/或生物地理上的区别的模式表明,六种或七种A. variabilis样的类,包括克雷伯氏菌。但是,由于我们在变异曲霉类之间未发现直接的形态学差异,因此目前我们拒绝将它们描述为一系列新物种。一个新属,Microcephaloides。例如,对于早先分配给瓦氏曲霉的ces虫,提出了建议。 variabilis,A。tenoramuraiaee Genov&Georgiev,1988年和P. krebsi。提供了对类型变种M. variabilis n。的重新描述。梳子,来自地鼠(Geomys spp。和Thomomys spp。)。除了1927年的无头颅虫(Basnonocephalcephaloides Baer)和1996年的Microcephaloides,古利亚耶夫(Paranoplocephaloides Gulyaev),1951年的Flabelloskrjabinia Spasskii以及1990年的Leporidotaenia Genov,Murai,Georgiev&Harris的有效属之外,1976年以前被认为是无头颅突耳的足动物(sensu) 。宿主谱和当前的系统发育数据表明,小头类目虫主要与田鼠(田鼠(Microtus spp。))有关,并且其基础谱系现在发生在土耳其的根特桑(M. guentheri)(Danford&Alston)。尽管基础谱系的分布和当前寄主表明其起源于古北洋西部,但随后的多样化可能发生在贝林吉亚东部,因为多数衍生谱系大部分都部分或全部发生在阿拉斯加。

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