The ultrastructure of the postcorpus of the putative outgroup of Secernentea (Nematoda), Teratocephalus lirellus (Teratocephalida), is compared with previous observations of representative species Zeldia punctata (Cephalobina), Caenorhabditis elegans (Rhabditina), and Diplenteron sp. (Diplogastrina) in order to interpret the evolution of feeding structures within Secernentea. The postcorpus of T. lirellus consists of 6 marginal, 13 muscle, 3 gland, and 11 nerve cells. In both T. lirellus and Z. punctata, one duct from each of two subventral glands opens into the esophageal lumen at the junction of the isthmus and the basal bulb, whereas in C. elegans and Diplenteron sp., homologous openings are at the posterior end of the median bulb. Caenorhabditis elegans and Z. punctata each have two additional glands that open within the basal bulb. The postcorpus of each taxon has four anterior-to-posterior layered sets of radial muscle cells, except in Diplenteron sp., which lacks a grinder and has homologs to the anterior two sets only. The anterior set of muscles of T. lirellus and Z. punctata includes six mononucleate cells, whereas the homolog in C. elegans and Diplenteron sp. includes three binucleate cells. Evaluation of character polarity defines Rhabditina and Diplogastrina as sister taxa, and suggests that the character of five glands may result from functional convergence.

The ultrastructure of the post-corpus of Zeldia punctata (Cephalobina) was compared with previous observations of Caenorhabditis elegans (Rhabditina) and Diplenteron sp. (Diplogastrina) with the goal of interpreting the morphological evolution of the feeding structures in the Secernentea. The post-corpus of Z. punctata consists of six marginal, 13 muscle, ¢ve gland and seven nerve cells. The most anterior of four layers of muscle cells consists of six mononucleate cells in Z. punctata. The homologous layer in C. elegans and Diplenteron consists of three binucleate cells, suggesting a unique derived character (synapomorphy) shared between the Rhabditina and Diplogastrina. Contrary to Diplenteron sp. where we observed three oesophageal glands, Z. punctata and C. elegans have ¢ve oesophageal glands. We question this shared character as re£ecting a common evolution between the Cephalobina and Rhabditina, because there are strong arguments for functional (adaptive) convergence of the ¢ve glands in these bacterial feeders. Convergence is further suggested by the mosaic distribution of three versus ¢ve glands throughout the Nemata; this distribution creates di¤culties in establishing character polarity. Although morphological data are often laborious to recover and interpret, we nevertheless view`reciprocal illumination' between molecular and morphological characters as the most promising and robust process for reconstructing the evolution of the Secernentea and its feeding structures.