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The discharge of the material of the Reissner's fibre (RF) and the massa caudalis (MC) into the "meningeal spaces" has until now not been studied in detail and with the aid of the electron-microscope. It was generally assumed that the material of the MC disintegrates in the "meningeal spaces", but the nature and function of those spaces have not been established. The CNS of Ammocoetes ist encompassed by the meninx primitiva, which is the meningeal tissue of the lower vertebrates; the meninx does not differentiate during ontogeny into the pia mater and the arachnoides. In contrast, the meninx primitiva of mammals is the anlage in the ontogenetical sense of the leptomeninges in adult individuals. The results presented in this paper are valid for Ammocoetes only; Petromyzon and Myxine must be studied anew from a perspective which may be the result of our study. Of particular interest would be an anatomical analysis of these caudalmost structures of the CNS (Ampulla caudalis [AC], MC, neuropori, lacunae etc.) in Branchiostoma. The diameter of the RF of Ammocoetes is approximately 1.7 micron; this is not different from the diameter of the RF in adult individuals. In the AC the RF divides into several smaller fibres which eventually disintegrate and form the amorphous MC. In sagittal sections, the fibrillary structure of the RF is distinct. In cross sections the small fibres may appear as globules. The terminal part of the RF is very often coiled. The ependyma of the caudal part of the canalis centralis (CC) ist not remarkable; liquor contacting neurons are frequently found with their dendrites touching the RF. Liquor contacting neurons are never found in the ependyma of the AC. The ependymal cells of the dorsal part of the AC possess neither kinocilia or microvilli. The disappearance of these organelles begins in the dorsal part of the caudalmost segment of the CC. Most surprising is the distribution of the attachment devices which are probably desmosomes. In the ependyma of the caudal part of the spinal cord the attachment devices are typically situated; in the ependyma of the AC these devices are absent. We use the general term "attachment devices" until the nature of these devices has been clearly determined. In the caudalmost part of the spinal cord as well as in the AC, the intercellular spaces between the ependymal cells communicate, forming a 3-dimensional labyrinth. If there are no attachment devices between the proximal parts of the ependymal cells, the intercellular spaces may provide a passageway between the CC and the loose tissue of the meninx primitiva.(ABSTRACT TRUNCATED AT 400 WORDS)

The microscopic anatomy of the sublingua of Tupaia glis was studied comparatively to find out if there is any possible explanation of the origin and the structural characteristics of the sublingual organ in Callicebus. The sublingua of Tupaia is at a primitive stage, but has nothing at all in common with the sublingual organ. The frenal lamella is not remarkable in this species. There are reasons to assume that the sublingual organ is a modified frenal lamella developed only in Callicebus.

Two kinds of secretion are formed in cells of the subcommissural organ (SCO) of Cebus apella. The "light secretion" is found in saccules originating from the endoplasmic reticulum. This secretion is stored in the peripheral portion of the cells and is not involved in formation of Reissner's fiber (RF). In close association with the Golgi complex, electron-dense granules are developed, containing a finely granular substance. These granules accumulate beneath the apical plasmalemma of the cell. Their content is discharged into the third ventricle, where it occurs in the form of a thin layer of secretion. This material appears to constitute the RF at the level of the entrance to the mesencephalic aqueduct.

The macro- and microscopic anatomy of the nasal fossa of Tupaia glis was compared with those of some insectivores. No significant group differences were found as far as the intranasal structures are concerned. Since the number of receptor cells in the olfactory epithelium of Tupaia glis and Talpa europaea is smaller than in the other species studied, a slight reduction of the sense of smell is suggested.

In a previous paper, the concept of the terminal organ (TO) of the subcommissural complex was forwarded. Functionally this complex is a neuro (glio-) hemal organ which serves to discharge the Reissner's secretory material into the systemic circulation. The TO is characterized by structural specializations that make feasible the discharge and chemical decomposition of the secretory material stowed in the massa caudalis (MC). The TO is probably not only the ampulla caudalis (AC); it may comprise even parts of the filum terminale next to the AC. The boundary of the TO is uncertain as yet. It cannot be precluded that the AC, which itself varies in shape and size, is just a receptaculum massae caudalis. The material of the MC escapes from the AC either through apertures of the wall of the AC or of the filum terminale (Neuropori caudalis, slit-shaped gaps). It is also likely that the secretory material becomes chemically decomposed in the AC and is intra- (trans-) cellularly discharged. In this connexion, certain ependymal cells may be of significance. These cells exhibit large, tongue-shaped central projections (temporarily developed?) which bear a considerable number of long microvilli. The significance of these cells probably lies in the enlargement of the cell surface bathing in the CSF which contains the MC. These cells are most abundant in the area of the TO; single, isolated cells of the same type occur in other areas of the ependyma of some primates. This would indicate that the TO does not contain special types of cells not found in other parts of the ependyma, but that the TO differs from other ependymal regions in the density of peculiar cell types.

The regio olfactoria of the mole, Talpa europaea, was studied by scanning and transmission electron microscopy. Peculiar structural differentiations, i.e. ovoid-shaped, balloon-like protuberances were found on the surface of the supporting cells. The apical portion of these protuberances contained finely dispersed granular material, whereas in their central part vesicular extensions of the smooth endoplasmic reticulum were observed.