population history

Lohse K, Barton NH, Melika G & Stone GN 2012 A likelihood-based comparison of population histories in a parasitoid guild. Mol Ecol 21:4605-4617.

  • if we want to actually test how concordant spatial histories are between species, we need a statistical, model-based framework
  • minimal triplet samples are of course uninformative about the parameters of current populations
  • they do contain information about the historical relationships of these populations and are amenable to exact likelihood analysis
  • the likelihood of a particular model can be maximised directly from the mutational patterns observed across arbitrary numbers of unlinked loci without loss of information
  • even with multiple (10–18) independent loci it is surprisingly difficult to distinguish between simple alternative divergence histories
  • this is despite the fact that unlike methods that rely on summaries of the data (summary statistics or gene trees), our likelihood calculation uses all available information
  • the historical signal contained in sequence data is inherently limited if histories are young
  • despite this, there is no shortage of phylogeographic studies that claim to find signatures of much more complex histories than those we were able to investigate here
  • few of these provide statistical tests for the historical scenarios they try to infer
  • recent histories are hard (or indeed impossible) to resolve using tens of loci
  • when increasing the number of loci by an order of magnitude even recent Pleistocene histories can be inferred
  • there is much scope for increasing the realism of model based inference
  • analogous expressions for the likelihood of triplet genealogies under more complex models including population size changes, migration and admixture can be derived
  • because of the inherent stochasticity of the coalescent, large volumes of data are required to have any hope to distinguish such more realistic models from simpler alternatives in practice