Ultrastructural studies of spermiogenesis of the clamLucina pectinata (Bivalvia, Lucinidae) from Northern Brazil

Spermatogenesis and sperm ultrastructure of the clam Lucina pectinata (Lucinidae) from northern Brazil were studied using light and transmission electron microscopy. The uniflagellate spermatozoa are grouped into characteristic rings within somatic cells (Sertoli-like cells), with the acrosome oriented toward the peripheryof these cells. The spermatozoa are long cells of the primitive type (ect-aquasperm) with a total length of 50.2 ± 2.5 mm, consisting of head (acrosome + nucleus), midpiece and tail. Acrosome is formed by an, acrosomal vesicle with a conical cylinder-like shaped (0.9 ± 0.1 mm length and 0.4 ± 0.1 mm in basal diameter) having a deeply infolded basis occupied by the subacrosomal space, containing flocculent material without axial rod. The acrosomal vesicle is formed by a membrane-bounded containing a broad basal ring of electron-dense material. The nucleus (7.5 ± 0.8 mm long) is an elongated, subcylindrical rod-shaped, slightly and gently curved, with a basal invagination (0.2-0.4 mm). It contains dense chromatin without any electron-lucent lacunae.The midpiece (1.0 ± 0.3 mm long; 1.1 ± 0.2 mm width) consist of four equal mitochondria located at the same level, surrounding two centrioles arranged at right angles. The proximal centriole lies at 90° relative the distal centriole and sperm longitudinal axis. The tail (40.5 ± 2.1 mm long) contains the common 9 + 2 pattern which in tapering end piece is successively reduced and sheated by the plasmalemma.

The effect of short-wavelength ultraviolet light on antigens, lection receptors and the ultraestructure of Crithidia fasciculata

Crithidia fasciculata is an important trypanosomatid parasite commonly affecting insects and is used extensively as a model for the study of the biochemistry, ultrastructure and organization of the kDNA network of trypanosomatids. The present study describes the evolution of UV-induced morphological changes detectable by transmission electron microscopy in Crithidia fasciculata. Although only rare and minor changes in Kinetoplast DNA were demonstrable 7 h after UV irradiation, alterations of this orgtanelle were present in almost al flagellates observed 24 h and 48 h after irradiation. Other cell structures were apparently undamaged. Ultrastructural changes in kDNA did not correspond to changes in antigenicity of protein bands in western blotting against serum from Chagas' disease patients or in the presence of 3 different lectin receptors on the surface of the parasite