Bisexual gonads in the stoneflies Perla burimeisteriana, P. pallida and Dinocras cephalotes are reported for the first time. Gross morphology and ultrastructure of the accessory ovaries of mature larvae and adult males of Perla marginata are described in detail. There are 36-58 male ovarioles situated distal to the paired testes and opening into fused termini of the lateral ducts in abdominal segments II and III. These correspond in structure to the ovarioles of adult females but are significantly smaller (maximum size of proximal oocyte 9.0 × 45 µm) and each usually contains 10-14 linearly arranged previtellogenic oocytes. Oogenesis ceases at the end of previtellogenesis or at the onset of vitellogenesis. The ooplasm contains either regularly dispersed or irregularly accumulated particles in different regions of the cell with accumulations occurring near mitochondria and Golgi complexes. Based on results of metachromatic staining, these are thought to represent either lipid droplets (most) or yolk globules. The oolemma rarely develops short microvili and few pycnotic vesicles. Development of the follicular epithelium (influencing vitellogenesis and secretory activity during choriogenesis) is abnormal. Follicular cell growth is not synchronized with that of the oocytes, and the follicular cells of the terminal (distal) oocytes show neither patency nor secretory activity. The mechanism controlling degeneration of male ovarioles and the evolutionary significance of hermaphroditic gonads in the Plecoptera are discussed.
The vitellogenesis of Paraechinophallus japonicus (Yamaguti, 1934), the first pseudophyllidean tapeworm of the family Echinophallidae studied using transmission electron microscope, is described on the basis of ultrastructural observations of specimens from the benthopelagic fish Psenopsis anomala (Temminck et Schlegel, 1844) (Perciformes: Centrolophidae). The process of vitellogenesis in P. japonicus follows the same general pattern observed in other tapeworms. Five stages of vitellocyte development have been distinguished. The first stage corresponds to immature cells containing ribosomes and mitochondria. The second stage of development is characterized by the appearance of granular endoplasmic reticulum and Golgi complexes, formation of shell globules and lipid droplets at the periphery of the cell cytoplasm. Vitellocyte of the third stage presents accumulation of shell globules and lipid droplets. During the fourth stage, shell globule clusters are formed, and lipid droplets and rosettes of α-glycogen are accumulated. Mature vitelline cells are characterized by a great number of lipid droplets with glycogen in the centre of the cytoplasm, whereas shell globule clusters are situated more peripherally. The interstitial tissue of vitelline follicles of P. japonicus is syncytial with long cytoplasmic projections extending between vitelline cells. The presence of a large amount of lipid droplets in the vitelline cytoplasm within the eggs of P. japonicus may be related to egg accumulation in the uterine sac.