Read K, Keogh J S, Scott I A, Roberts J D, Doughty P
School of Botany and Zoology, Australian National University, Canberra, ACT 0200, Australia.
Mol Phylogenet Evol. 2001 Nov;21(2):294-308. doi: 10.1006/mpev.2001.1014.
We present a mitochondrial gene tree for representative species of all the genera in the subfamily Myobatrachinae, with special emphasis on Crinia and Geocrinia. This group has been the subject of a number of long-standing taxonomic and phylogenetic debates. Our phylogeny is based on data from approximately 780 bp of 12S rRNA and 676 bp of ND2, and resolves a number of these problems. We confirm that the morphologically highly derived monotypic genera Metacrinia, Myobatrachus, and Arenophryne are closely related, and that Pseudophryne forms the sister group to these genera. Uperoleia and the recently described genus Spicospina are also part of this clade. Our data show that Assa and Geocrinia are reciprocally monophyletic and together they form a well-supported clade. Geocrinia is monophyletic and the phylogenetic relationships with the genus are fully resolved with two major species groups identified: G. leai, G. victoriana, and G. laevis; and G. rosea, G. alba, and G. vitellina (we were unable to sample G. lutea). We confirm that Taudactylus forms the sister group to the other myobatrachine genera, but our data are equivocal on the phylogenetic position of Paracrinia. The phylogenetic relationships among Crinia species are well resolved with strong support for a number of distinct monophyletic clades, but more data are required to resolve relationships among these major Crinia clades. Crinia tasmaniensis and Bryobatrachus nimbus form the sister clade to the rest of Crinia. Due to the lack of generic level synapomorphies for a Bryobatrachus that includes C. tasmaniensis, we synonymize Bryobatrachus with Crinia. Crinia georgiana does not form a clade distinct from other Crinia species and so our data do not support recognition of the genus Ranidella for other Crinia species. Crinia subinsignifera, C. pseudinsignifera, and C. insignifera are extremely closely related despite differences in male advertisement call. A preliminary investigation of phylogeographic substructure within C. signifera revealed significant divergence between samples from across the range of this species.
我们展示了肌蟾亚科所有属的代表性物种的线粒体基因树,特别着重于姬蛙属和地蛙属。该类群一直是诸多长期存在的分类学和系统发育学争论的主题。我们的系统发育基于约780 bp的12S rRNA数据和676 bp的ND2数据,并解决了其中一些问题。我们证实形态上高度特化的单型属——新姬蛙属、肌蟾属和澳蟾属亲缘关系密切,且伪姬蛙属构成这些属的姐妹群。强蛙属和最近描述的针棘蛙属也是该分支的一部分。我们的数据表明,阿萨姬蛙属和地蛙属互为单系类群,它们共同构成一个得到充分支持的分支。地蛙属是单系类群,与该属的系统发育关系已完全明确,识别出两个主要物种组:利氏地蛙、维克托地蛙和光滑地蛙;以及玫瑰地蛙、白氏地蛙和卵黄地蛙(我们未能采集到黄斑地蛙样本)。我们证实,胃囊蛙属构成其他肌蟾亚科属的姐妹群,但我们的数据在副姬蛙属的系统发育位置上并不明确。姬蛙属物种间的系统发育关系已得到很好的解析,多个不同的单系分支得到有力支持,但需要更多数据来解析这些主要姬蛙属分支之间的关系。塔斯马尼亚姬蛙和云雾澳蟾构成姬蛙属其他物种的姐妹分支。由于包含塔斯马尼亚姬蛙的澳蟾属缺乏属级共衍征,我们将澳蟾属与姬蛙属同义。乔治亚姬蛙并未形成一个与其他姬蛙属物种不同的分支,因此我们的数据不支持将其他姬蛙属物种归为泽姬蛙属。尽管雄性求偶鸣叫存在差异,但微小姬蛙、拟微小姬蛙和姬蛙极为密切相关。对姬蛙种内系统地理学亚结构的初步调查显示,该物种分布范围内不同样本之间存在显著分化。