The structure of the intestine and its adnexa in the Australian lungfish Neoceratodus forsteri (Krefft), is described from four adult specimens and compared with that of other lungfish. In all lungfish genera the intestine is thick and straight and contains a complicated spiral valve; a pyloric fold separates the foregut from the midgut. In Neoceratodus the coiling of the intestinal lumen begins in the prepyloric or gastric region, unlike in other vertebrates with a spiral valve, where it begins behind the pylorus. The spiral valve of Neoceratodus begins as a deep groove on the right side of the foregut, just behind the glottis. Such a prepyloric groove is present but poorly developed also in the lungfishes Protopterus and Lepidosiren and contains a prepyloric spleen in all genera. A separate postpyloric spleen is situated in the free margin of the spiral valve, i.e. in the axis of the intestine. The spleen has a heavily pigmented cortex containing large amounts of iron. The pancreas, buried in the spiral valve in front of the pylorus in Neoceratodus, contains numerous islets of Langerhans, similar to those of tetrapods. This is unexpected because the islets ofProtopterus, described by Gabe in 1969, are more like the large, encapsulated “Brockmann bodies” of teleosts.

Choanocyte‐like cells with a collar of regularly arranged cylindrical microvilli around the base of the flagellum were observed in the ciliary bands of the Brachiolaria larva of Asterias rubens. The ambulacral ampullae and coelomic epithelia of adult Asterias and coelomic epithelia of Mesothuria contain similar cells with radial lamellae instead of cylindrical microvilli. Other similar but more modified types of cells, in which the inner edges of the radiating lamellae could be recognized as longitudinal ridges in the wall of a cylindrical flagellar pit, were found in ambulacral ampullae of Porania and in coelomic epithelia of Stichopus. Distinct indications of phagocytosis were seen in most of these cells. The present report together with previously published data lend support to the idea, that the choanocyte is a fundamental cell type in metazoans, probably derived phylogenetically from some flagellate ancestor.

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The spermatozoa of Petrobius and Lepisma share a few general insect features (filamentous shape, two mitochondria, compact acrosome vesicle, bilateral symmetry) but differ fundamentally with regard to specializations. In Petrobius, a long coiled acrosome, a coiled nucleus, and a “body” with axonema, two mitochondria, and a pair of lateral bodies follow each other in normal sequence. In Lepisma the acrosome is a small vestige in the spoon‐shaped anterior end, the centriole is dislocated anteriorly, and nucleus, two mitochondria and axonema run like parallel filaments through most of the spermatozoon. The centriole adjunct develops into a postnuclear body in Lepisma but forms a pair of complicated “lateral bodies” in Petrobius. It is concluded that ancestral forms must have had fairly primitive spermatozoa and that specialization has proceeded independently within each evolutionary line.