, Volume 92, Issue 3, pp 121–127

Phylogeography of Australia’s king brown snake (Pseudechis australis) reveals Pliocene divergence and Pleistocene dispersal of a top predator


    • Zentrum der RechtsmedizinKlinikum der Johann Wolfgang Goethe-Universität
  • J. Scott Keogh
    • School of Botany and ZoologyAustralian National University
  • John Weigel
    • Australian Reptile Park
  • Laurie A. Smith
    • Department of Terrestrial VertebratesMuseum of Natural Science
  • Dietrich Mebs
    • Zentrum der RechtsmedizinKlinikum der Johann Wolfgang Goethe-Universität
Short Communication

DOI: 10.1007/s00114-004-0602-0

Cite this article as:
Kuch, U., Keogh, J.S., Weigel, J. et al. Naturwissenschaften (2005) 92: 121. doi:10.1007/s00114-004-0602-0


King brown snakes or mulga snakes (Pseudechis australis) are the largest and among the most dangerous and wide-ranging venomous snakes in Australia and New Guinea. They occur in diverse habitats, are important predators, and exhibit considerable morphological variation. We infer the relationships and historical biogeography of P. australis based on phylogenetic analysis of 1,249 base pairs from the mitochondrial cytochrome b, NADH dehydrogenase subunit 4 and three adjacent tRNA genes using Bayesian, maximum-likelihood, and maximum-parsimony methods. All methods reveal deep phylogenetic structure with four strongly supported clades comprising snakes from New Guinea (I), localities all over Australia (II), the Kimberleys of Western Australia (III), and north-central Australia (IV), suggesting a much more ancient radiation than previously believed. This conclusion is robust to different molecular clock estimations indicating divergence in Pliocene or Late Miocene, after landbridge dispersal to New Guinea had occurred. While members of clades I, III and IV are medium-sized, slender snakes, those of clade II attain large sizes and a robust build, rendering them top predators in their ecosystems. Genetic differentiation within clade II is low and haplotype distribution largely incongruent with geography or colour morphs, suggesting Pleistocene dispersal and recent ecomorph evolution. Significant haplotype diversity exists in clades III and IV, implying that clade IV comprises two species. Members of clade II are broadly sympatric with members of both northern Australian clades. Thus, our data support the recognition of at least five species from within P. australis (auct.) under various criteria. We discuss biogeographical, ecological and medical implications of our findings.

Supplementary material

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Copyright information

© Springer-Verlag 2005