Award details

Total evidence in phylogentic inference: a test of principle using the Crustacea

ReferenceBB/C006682/1
Principal Investigator / Supervisor Professor Matthew Wills
Co-Investigators /
Co-Supervisors
Professor Richard Ffrench-Constant, Professor Laurence Hurst
Institution University of Bath
DepartmentBiology and Biochemistry
Funding typeResearch
Value (£) 259,740
StatusCompleted
TypeResearch Grant
Start date 09/05/2005
End date 08/09/2008
Duration40 months

Abstract

The need for large, well supported phylogenies as the basis for rigorous comparative, biodiversity and evolutionary analyses has never been greater. There are principally two methods for improving the scope and or robustness of trees. Supertree methods combine trees rather than raw data, each tree the product of an independent parsimony or likelihood analysis. Total evidence, by contrast, derives a supermatrix that can comprise raw data from many molecules and morphology, and subjects this to a single tree-building analysis. The topologies resulting may differ from any of those derived from the investigation of subsets of the data, and branch support values are often significantly enhanced. Another compelling defence of total evidence centres on its purported ability to recover weak phylogenetic signals and improve resolution at multiple levels. Examples in the literature are usually of a limited scale, and often derive a stable topology when data from a small number of sources are combined. We will attempt a proof of principle here by applying total evidence to one of the most recalcitrant phylogenetic problems within the Metazoa: the relationships of crustaceans. In this group, the piecemeal addition of data from new molecules and from additional taxa has thus far only served to muddy the water. Rather than reinforcing support and converging on a single resolution, there is now uncertainty concerning the monophyly or paraphyly of the group, the integrity of most orders and nearly all inter-ordinal relationships. What is needed is markedly more diverse character and taxon sampling throughout the crustaceans and their closest relatives. We will greatly improve coverage down to the subordinal level for six established phylogenetic markers: 18S, 28S, 16S, COI, Elongation factor 1 alpha, RNA Polymerase II. We will also generate important new data for five hitherto underutilised phylogentic markers: G3PDH, PEPCK, Enolase, Elongation factor 2, alpha-Tubulin 1. We will collate and extend existing morphological data sets, and include data on important fossil genera. When complete, this will represent the largest and most diverse phylogenetic character set ever complied for the crustaceans. Partitions of the data will be analysed independently to compare their signals. All data will be analysed simultaneously using parsimony and likelihood approaches, and the robustness of the resulting trees will be assessed using bootstrapping and branch support indices. Results from total evidence analyses will be compared with supertrees.

Summary

unavailable
Committee Closed Committee - Genes & Developmental Biology (GDB)
Research TopicsX – not assigned to a current Research Topic
Research PriorityX – Research Priority information not available
Research Initiative X - not in an Initiative
Funding SchemeX – not Funded via a specific Funding Scheme
terms and conditions of use (opens in new window)
export PDF file