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The prostomium alone or the prostomium and proventriculus of reproductiveTyposyllis pulchra were periodically removed at known stages of oogenesis and the gametes were examined by transmission electron microscopy. If the proventriculus and prostomium were simultaneously removed prior to day 3 of the stolonization sequence, before gonial differentiation, the time reruired for stolon formation and concomitant gametogenesis was shortened; the animals, all of which had previously reproduced as females, produced only ultrastructurally normal sperm. Spermatogenesis in these induced males began earlier in the stolonization period than in normal males. However, the cytological events of spermatogenesis were not accelerated. When the same operation was performed after differentiated oocytes were present, gamete cytodifferentiation and development time did not appear to be affected and the animals remained female. Removal of the prostomium alone, formerly thought to have no effect, caused high mortality and if removed prior to day 3 appeared to prevent both stolonization and gametogenesis. Ultrastructural investigation of these animals shows that gonads are maintained, but that gonial cells fail to differentiate or produce gametes. The subsequent removal of the proventriculus and regenerating prostomium from these animals allows them to mature as induced males. This suggests a prostomial role in regulating the endocrine activity of the proventriculus during the reproductive cycle.

Tryposyllis pulchra reproduces by the production of three to four gamete-bearing stolons (schizogamy) during consecutive 30--day periods. Although gonads are found in a large number of segments, only those in the posterior-most segments produce gametes and become incorporated into the developing stolon. The more anterior gonads remain undifferentiated and probably sexually undetermined until they are needed in future stolonizations. Gonial cells, which will eventually become either male or female, are ultrastructurally identical at the onset of each stolonization period. Spermatogenesis is marked by a short proliferative period followed by differentiation and spermiogenesis. The first ultrastructural signs of spermatogenesis were found in coelomic spermatogonia on day 10 of stolon formation. Spermatogonia are joined by intercellular bridges, which are maintained until the early spermatid stage. Synaptonemal complexes mark the onset of meiosis, which is apparently synchronized in the syncytial clusters of primary spermatocytes. Spermiogenesis occurs during the final 10 days of stonolization and a variety of stages is present within a single animal. All sperm mature by the time the stolon detaches. Acrosome formation and nuclear condensation are described in addition to the ultrastructure of mature sperm.

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