Ancient habitat shifts and organismal diversification are decoupled in the African viper genus Bitis (Serpentes: Viperidae)

作者: Axel Barlow , Wolfgang Wüster , Christopher M. R. Kelly , William R. Branch , Tony Phelps

DOI: 10.1111/JBI.13578

关键词: CladogenesisAllopatric speciationEcologyMonophylyBitis caudalisBiologyWoodlandCoalescent theoryBitisSpecies complex

摘要: Aim: The expansion of open habitats during the mid-Miocene has been hypothesized as a driver allopatric speciation for many African taxa. This habitat-dependent mode diversification implicated in shift from C3 (e.g. forest/woodland) to C4 dominated systems (i.e. savanna, grasslands) number squamates. We examined this hypothesis using genus viperid snakes (Bitis) with both habitat and forest-dwelling representatives. Location: Africa. Methods: A comprehensive multilocus dataset was used generate calibrated species tree multispecies coalescent model. Individual gene trees patterns nuclear allele sharing were assess monophyly isolation. To test evolution hypothesis, we generated an ancestral character state reconstruction closed dated phylogeny. related timing forest/woodland contraction Results: Bitis originated Oligocene, level late Miocene/Pliocene. Four well-supported clades correspond recognized subgenera Bitis, Keniabitis, Macrocerastes Calechidna. Several previously unrecognized lineages potentially represent cryptic species. Main conclusions Habitat-dependent does not appear have main generic viperine diversification: at least one clade moved into forest Miocene, long after had contracted fragmented. Forest-dependent diversified only presumably became further reduced extent, fitting model speciation. Although our results do favour general pattern cladogenesis within subgenus Calechidna “arenicolous” (Bitis caudalis complex) “rupicolous” (B. Atropos-cornuta complex), corresponds aridification southwest suggests there are subtleties captured broad category, which relevant understanding role evolution.

参考文章(81)
Godfrey M Hewitt, The structure of biodiversity – insights from molecular phylogeography Frontiers in Zoology. ,vol. 1, pp. 4- 4 ,(2004) , 10.1186/1742-9994-1-4
Jérôme Fuchs, Juan L Parra, Steven M Goodman, Marie Jeanne Raherilalao, Jeremy Vanderwal, Rauri CK Bowie, None, Extending ecological niche models to the past 120 000 years corroborates the lack of strong phylogeographic structure in the Crested Drongo (Dicrurus forficatus forficatus) on Madagascar Biological Journal of The Linnean Society. ,vol. 108, pp. 658- 676 ,(2013) , 10.1111/J.1095-8312.2012.02022.X
Liam J. Revell, phytools: an R package for phylogenetic comparative biology (and other things) Methods in Ecology and Evolution. ,vol. 3, pp. 217- 223 ,(2012) , 10.1111/J.2041-210X.2011.00169.X
Yan Yu, A.J. Harris, Christopher Blair, Xingjin He, RASP (Reconstruct Ancestral State in Phylogenies): A tool for historical biogeography Molecular Phylogenetics and Evolution. ,vol. 87, pp. 46- 49 ,(2015) , 10.1016/J.YMPEV.2015.03.008
M. H. Trauth, Late Cenozoic Moisture History of East Africa Science. ,vol. 309, pp. 2051- 2053 ,(2005) , 10.1126/SCIENCE.1112964
E. S. Vrba, Mammals as a Key to Evolutionary Theory Journal of Mammalogy. ,vol. 73, pp. 1- 28 ,(1992) , 10.2307/1381862
Shelley Edwards, Bieke Vanhooydonck, Anthony Herrel, G. John Measey, Krystal A. Tolley, Convergent Evolution Associated with Habitat Decouples Phenotype from Phylogeny in a Clade of Lizards PLoS ONE. ,vol. 7, pp. e51636- ,(2012) , 10.1371/JOURNAL.PONE.0051636
Howard D. Rundle, Patrik Nosil, Ecological speciation: Ecological speciation Ecology Letters. ,vol. 8, pp. 336- 352 ,(2005) , 10.1111/J.1461-0248.2004.00715.X