Histomorphology of the proventriculi of nectarivorous, granivorous and omnivorous passerines was studied. The proventriculus consisted of mucosal, submucosal, muscularis and serosal layers. Proventricular wall was thickest in omnivore, thinnest in granivore and intermediate in nectarivore. The openings of mucosal glands had a single spiral-like fold of mucosa in the omnivorous Silvereye, 2-3 spirals in the granivorous Zebra finch and 4-5 spirals in the nectarivorous Brown honeyeater. The mucosal glands were arranged in a uniform row in the wall of the organ and opened individually via a primary duct to the lumen of the proventriculus. The surface epithelial cells of the tunica mucosa contained secretory cells and the proventricular glands contained endocrine, neck and oxynticopeptic cells. The ultrastructural features of the oxynticopeptic cells changed from the oral to the aboral portion of the gland. In the oral region, the cytoplasm presented numerous, smaller (600-900 nm) homogenously dense zymogen secretory vesicles and larger (0.8-2.3 microm) pale floccular, tubular, mucin-like secretory granules, few small mitochondria and RER while in the aboral portion of the gland, the cytoplasm presented numerous, large mitochondria with closely packed cristae, secondary lysosome and infolding of the basal and apical cell membrane. The tunica sub mucosa was thin with occasional large blood vessels. The tunica muscularis consisted of inner longitudinal, middle circular and outer longitudinal layers. The external tunica serosa contained large bundles of myelinated and unmyelinated axons that were possibly branches of the intestinal nerve. The structural adaptations of the proventriculi of these three species to their various diets are discussed.

Our current understanding of clathrin-mediated endocytosis proposes that the process is initiated at a specialized anatomical structure called a coated pit. Electron microscopy has been required for elucidation of the morphology of coated pits and the vesicles produced therein, and the presence of a bristle coat has been taken as suggestive of clathrin surrounding these vesicles. More recently, immunocytochemical methods have confirmed that endocytic vesicles are surrounded by clathrin and its adaptor proteins, but there is a need to identify precisely and to follow the fate of the cellular organelles seen by fluorescence microscopy. We used quantum immune-electron microscopy to localize clathrin in a human adrenal cortical cell line (SW-13). Clathrin was shown to associate with a variety of vesicle types including the classic clathrin-coated vesicles and pits used in receptor internalization, pentilaminar annular gap junction vesicles, and multivesicular bodies. The images obtained with quantum dot technology allow accurate and specific localization of clathrin and the clathrin adaptor protein, AP-2, with cellular organelles and suggest that some of the structures classified as typical coated vesicles by immunocytochemical light microscopic techniques actually may be membrane bound pits.

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