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Gametogenesis in Chitonida is highly unusual, giving rise to eggs with elaborate, often spiny hulls and sperm with needle-like nuclear extensions and tiny acrosomes. My studies of oogenesis in a variety of chitonid families have revealed unique mechanisms of egg hull formation. Three-dimensional reconstruction of serial sections of oogenesis in the chitonidAcanthochitona garnoti(Blainville) confirms that the egg hull is formed largely by microapocrine secretions, rather than by exocytosis of Golgi vesicles. This novel process, detailed for the first time in Mollusca, bypasses the endomembrane system and releases compounds formed in the cytoplasm directly from the cell surface via budding of ‘microaposomes’. Fertilization is no less unusual. In virtually all Metazoa, except chitonids, the entire sperm enters the egg, and sperm mitochondria are digested. Typically, the centrosome that derives from the sperm centriole acts as a microtubule organizing centre, moving the two pronuclei together to form the zygote nucleus and later initiating cleavage of the embryo. However, in chitonids the sperm digest a minute pore in the egg hull that allows injection of DNA but blocks entry of sperm organelles, including the nuclear membrane. Serial sections of fertilized eggs ofMopalia muscosa(Gould) confirm that a membrane bag, abandoned on the egg surface, contains the sperm organelles. Thus, not only is there maternal inheritance of mitochondria and centrioles in Chitonida but also other sperm proteins normally associated with fertilization may be blocked from entering the egg. [ABSTRACT FROM AUTHOR]

Early events of fertilization are described in Chaetopleura apiculata and other selected Chitonida. C. apiculata egg hulls are elaborated into multi-branched spines with interlocking polygonal bases. Around the perimeter of each base are a series of open pores, ranging in size from 0.1-0.5 µm, which permit sperm direct access to the vitelline layer. In Callochitonidae (Chitonida) even larger pores occur in egg jelly coats, but this is considered to be the plesiomorphic condition, found also in Lepidopleurida such as Deshayesiella curvata. Other Chitonina, such as Rhyssoplax tulipa and Acanthopleura granulata, have a continuous outer dense layer that lacks pores and must be digested by penetrating sperm. Fertilization in Chitonida is unique and involves injection of chromatin into the egg via a narrow tubular nuclear extension that appears to exclude other sperm organelles, including mitochondria, centrioles, and flagellum. New evidence from studies of fertilization in Mopalia muscosa (Chitonida: Acanthochitonina) supports this hypothesis. This type of fertilization implies maternal inheritance of both mitochondria and centrioles, which is highly unusual, because in most animals one sperm centriole assists movements of pronuclei and regulates organization of the mitotic spindle. This mechanism of fertilization is defined by a series of apomorphic characters that unify the order Chitonida. [ABSTRACT FROM AUTHOR]