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Phylogeny and Evolution of Rhabditid Nematodes<br />

Kiontke, K. & D. Fitch<br />

Department of Biology, New York University, New York, NY 10003, USA<br />

A new, multigene molecular phylogeny resolves most relationships among major groups of<br />

rhabditid nematodes and provides a framework for studying character evolution. In this<br />

phylogeny, rhabditids are paraphyletic with regard to Strongylida and diplogastrids. The first<br />

branch is Poikilolaimus and there are three major clades: (1) ‘Eurhabditis’, which includes<br />

Caenorhabditis and its sister ‘Protorhabditis group’ (which includes Diploscapter), the<br />

‘Rhabditis group’ (including Oscheius, strongylids, Heterorhabditis, and other clades) and<br />

Choriorhabditis; (2) Rhabditoides inermis + diplogastrids; and (3) ‘Pleiorhabditis’, which<br />

includes Rhabditoides inermiformis, Rhabditoides regina, Pelodera, and the ‘Mesorhabditis<br />

group’ (which includes Parasitorhabditis). The phylogeny reveals that many characters have<br />

evolved convergently; e.g., reproductive mode, intron positions, developmental characters,<br />

and parts of male tail morphology. However, a number of morphological and developmental<br />

characters demonstrate high consistency with the molecular phylogeny, providing additional<br />

support for several clades. For example, a slit-shaped vulva is apomorphic for ‘Eurhabditis’;<br />

the orientation of a cell division in the 2-cell embryo flipped 90˚ in the ancestor to the<br />

Protorhabditis group; species in the Mesorhabditis group share a posterior vulva and<br />

prodelphy; and a pharynx lacking a median bulb is derived and evolved only once in<br />

rhabditids. Several previously defined taxa correspond with monophyletic groups (e.g.,<br />

Oscheius, Caenorhabditis, Pelodera, and Poikilolaimus sensu Sudhaus) or paraphyletic<br />

groups (e.g. Protorhabditis with respect to Diploscapter and Prodontorhabditis). Some other<br />

taxa are polyphyletic (e.g. Pellioditis, Rhabditis, and Rhabditoides). To support systematic<br />

research and studies in comparative biology and character evolution, we continue to build a<br />

representative living collection of rhabditid species (currently ~140). Current efforts are<br />

focused on finer phylogenetic resolution. Future goals are to develop a classification system,<br />

an electronic key, and a systematics database for rhabditids.<br />

Turning Trees into Taxonomies<br />

Adams, B.J.<br />

Department of Microbiology & Molecular Biology, and Evolutionary Ecology Laboratories, Brigham Young<br />

University, Provo, UT.<br />

What began with Plato and Aristotle (and arguably much earlier) and was ultimately<br />

canonized by Linné, culminated in a conflict that continues to this day, namely, what is the<br />

best way to classify life on earth? Ever since Darwin, the idea that all species can be depicted<br />

in a hierarchical tree of successively more inclusive groups has been a driving force behind<br />

the movement to produce taxonomies that are consistent with evolutionary history<br />

(phylogeny). Few quibble against the utility of such taxonomy. However, arguments over<br />

the best way to accomplish this goal have been most acrimonious. Key to the proposed<br />

solutions is the philosophical questions of whether natural groups exist independent of human<br />

observation, and how they should best be reflected in taxonomic systems. I discuss<br />

competing approaches in a historical context, and provide examples to demonstrate that<br />

Linné’s 273 year-old system, with some modification, is sufficient to accommodate<br />

monophyletic classification.<br />

5 th International Congress of Nematology, 2008 19

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