ASPECTS OF CILIARY FINE STRUCTURE IN EUPLOTES PATELLA

1. The functional unity of cirri and membranelles can result structurally only from extensions of the ciliary membrane. 2. The pellicle is composed of an outer pellicular membrane and an inner cytoplasmic membrane. 3. The ciliary rootlets are composed of numerous filaments 120 A in diameter with central areas of low density. They have no periodic structure. 4. The ciliary membrane is a double-layered structure continuous with the pellicular membrane. The cilia show the typical arrangement of nine double, peripheral and two single, central fibrils. All fibrils pass into the basal region, the peripheral ones joining with the rootlet filaments, while the central fibrils from the extreme proximal position of the basal region turn back toward the pellicle and appear to unite just beneath the cytoplasmic membrane. 5. The cilia (300 mµ diameter) taper at their tips to a diameter at least as small as 50 mµ. At a diameter of about 150 mµ, the fibrils begin to show a reduction in number. 6. The central ciliary fibrils may determine the possible directions of ciliary beat. These fibrils show an intrafibrillar structure in their basal portion, which involves regularly spaced 40 A granules. 7. These observations on Euplotes, together with the other evidence cited, are consistent with the hypothesis that ciliary motion is produced by the contraction of the peripheral fibrils, while the central fibrils perhaps determine the plane in which the cilia can bend.     

FINE STRUCTURE CHANGES DURING FUNCTION OF THE DIGESTIVE GLAND OF VENUS'S-FLYTRAP

Changes in the structure of the digestive gland cells of Venus's-flytrap during the digestive process have been studied with light and electron microscopy. Large vacuolar lipid-protein inclusions break up and become smaller; however, they never completely disappear during the entire 7-10-day cycle. Dictyosomes in the resting digestive gland are associated with small, inconspicuous vesicles, whereas during the digestive cycle two types of prominent vesicles are observed on the peripheral tubules. Changes in plastid fine structure are complex and involve the disappearance of lipid globules and the tubular complex, followed by the formation of microtubules on the thylakoids and cisternae on the outer plastid membrane. Mitochondrial fine structure changes from the small cristae and light matrix of the resting state to large cristae and a very dense matrix representative of a change to a state where phosphorylation is tightly coupled to electron transport. Pronounced changes which occur in the cell envelope (cell wall and membrane taken together) are apparently associated with secretion of the digestive fluid. Numerous other changes are observed such as polysome formation, multivesicular body formation, mitochondria division, and changes which can be attributed in general to elevated cell activity.     

THE FINE STRUCTURE AND FUNCTION OF THE SALIVARY GLANDS OF NUCELLA LAPILLUS (GASTROPODA: MURICIDAE)

The fine structure of the tubular and acinous salivary glandsof Nucella lapillus (L.) has been studied and some histochemicaland enzyme tests have been carried out. The clusters of subepithelialcells of the tubular glands secrete a glycoprotein composedof chains of tubular macromolecules resembling secretions knownto have adhesive properties which may assist in boring. Thesecretion is rich in disulphide groups, as are many toxins,and is believed to be responsible for the recently demonstratedpharmacological activity of the glands. It is proposed thatflaccid paralysis is induced in prey by envenomation with thissecretion during rasping, after soft parts have been exposedby an ‘anti-predator’ reaction to secretion fromthe hypobranchial gland of Nucella. The secretory vesicles ofboth types of gland cells in the acinous glands have heterogeneouscontents indicating that their secretions are complex. The majorcomponent in those of the mucous cells is an acid mucopolysaccharidetypical of a lubricant or releasing agent. The ciliated basalcells resemble typical enzyme-secreting cells and the majorconstituent of their secretion is a finely granular glycoprotein. (Received 8 January 1990; accepted 5 June 1990)     

THE FINE STRUCTURE OF CAPILLARIES AND SMALL ARTERIES

Details of capillary endothelia of the mammalian heart are described and compared with capillaries of other organs and tissues. Continuous invagination and pinching off of the plasma membrane to form small vesicles which move across the cytoplasm are suggested as constituting a means of active and selective transmission through capillary walls (12). This might be designated as cytopempsis (transmission by cell). The fine structure of the different layers in the walls of small heart arteries is demonstrated. Endothelial protrusions extend through windows of the elestica interna to make direct contact with smooth muscle plasma membranes. The elastica interna appears to vary greatly in both thickness and density, and probably restricts filtration, diffusion, and osmosis to such an extent that windows and the transport mechanisms described (cytopempsis) are necessary for the functional integrity of the smooth muscle layer. The contractile material consists of very fine, poorly oriented filaments.     

FINE STRUCTURE AND REPLICATION OF THE KINETOPLAST OF TRYPANOSOMA LEWISI

The kinetoplastic DNA of Trypanosoma lewisi is described as a filamentous body lying within a mitochondrion, with the filaments oriented parallel to the long axis of the cell. The manner of fixation, the replicative state, and perhaps the physiological state of the cell, may result in slight morphological differences among such bodies. The kinetoplastic DNA replicates to form "left" and "right" rather than "upper" and "lower" members, and both the kinetoplast and nucleus incorporate radiothymidine as shown by radioautography. Radioautographic analyses suggest a random incorporation of radiothymidine by kinetoplasts. Silver grains were occasionally observed over centriolar elements. Finally, the observations are discussed with respect to the sequential replication of the aforementioned organelles by T. lewisi.     

THE FINE STRUCTURE OF NEURONS

1. Thin sections of representative neurons from intramural, sympathetic and dorsal root ganglia, medulla oblongata, and cerebellar cortex were studied with the aid of the electron microscope. 2. The Nissl substance of these neurons consists of masses of endoplasmic reticulum showing various degrees of orientation; upon and between the cisternae, tubules, and vesicles of the reticulum lie clusters of punctate granules, 10 to 30 mµ in diameter. 3. A second system of membranes can be distinguished from the endoplasmic reticulum of the Nissl bodies by shallower and more tightly packed cisternae and by absence of granules. Intermediate forms between the two membranous systems have been found. 4. The cytoplasm between Nissl bodies contains numerous mitochondria, rounded lipid inclusions, and fine filaments.     

MORPHOLOGY,FINE STRUCTURE,AND ONTOGENY OF THE STINGING EMERGENCE OF URTICA DIOICA

Stinging emergences in Urtica dioica L. characteristically possess an elongate stinging cell and a multicellular pedestal. The emergence is derived from the epidermal and subepidermal cell layers. The apical wall of the stinging cell is composed of silica bodies which decrease basipetally in concentration. The basal portion of the cell wall of the stinging cell is devoid of silica bodies and lacks primary pit fields or pits between it and the pedestal cells. X-ray microanalysis of electron dense particles located in the stinging cell ER-golgi complex indicate that these particles contain silicon. There is no ultrastructural evidence for the presence of a toxin synthesizing system or a toxin itself.     

GENETIC STRUCTURE OF THE WESTERN NORTH AMERICAN AQUATIC GASTROPOD GENUS TAYLORCONCHA AND DESCRIPTION OF A SECOND SPECIES

The Bliss Rapids Snail (Taylorconcha serpenticola) is a threatenedspecies that ranges along a short reach of the middle SnakeRiver in southern Idaho. Additional Taylorconcha populationsof uncertain taxonomic status have recently been discoveredin other portions of the Snake River basin (Owyhee River, lowerSnake River). We investigated the phylogenetic relationshipsand population structure of these snails, together with twooutgroups, using cytochrome c oxidase subunit I (COI) of mitochondrialDNA and the first internal transcribed spacer region betweenthe 18S and 5.8S ribosomal DNA. These data show no sharing ofhaplotypes or genotypes among T. serpenticola and the Owyhee-LowerSnake populations, with both depicted as monophyletic unitswithin the Taylorconcha clade. Both of these datasets and morphologicalevidence suggest that the Owyhee-Lower Snake populations area distinct species, which we describe herein (T. insperata newspecies). Application of an available COI molecular clock suggeststhat Taylorconcha arose in the late Miocene, when ancestralSnake River drainage was impounded in an extensive lacustrinesystem (‘Lake Idaho’) in western Idaho. The shallowpopulation structuring of T. insperata suggests that the lowerSnake River was only recently colonized subsequent to incisionof Hells Canyon, draining of Lake Idaho, and development ofa through-going river in the late Neogene. The absence of significantgenetic structure in T. serpenticola, which is attributed tothe unstable course and flow regime of the middle Snake Riverduring the Quaternary, suggests that this species can be treatedas a single management unit. (Received 14 July 2005; accepted 23 September 2005)     

THE FINE STRUCTURE AND FUNCTION OF THE ANAL GLAND OF THE MURICID NUCELLA LAPILLUS (NEOGASTROPODA) (AND A COMPARISON WITH THAT OF THE TROCHID GIBBULA CINERARIA)

The fine structure of the anal gland of Nucella lapillus isdescribed, and compared with that of Gibbula cineraria. It isconcluded that the glands are not analogous in function andare unlikely to be homologous. The anal gland of Gibbula isa small rectal diverticu-lum near the anal papilla, lined bymucus-secreting cells. The evidence suggests that the largeanal gland of Nucella extracts macromolecules and cations fromthe blood, metabolizes or sequesters them in lyso-somes andultimately expels the resultant residual bodies by apocrinesecretion. It has large reserves of lipid and glycogen, andthe abundance of melanin indicates that it is a major site oftyrosine degradation. The invariable presence of bacteria inthe lumen, and of pits in the epithelium to house them, impliesa symbiotic relationship in which the bacteria metabolize anddegrade the cell debris, some of which is resorbed. The lossof the anal gland in bucci-nids and nassariids is accompaniedby great reduction in size and importance of the rectal sinus,and increase in complexity of the kidney. (Received 31 December 1991; accepted 23 January 1992)     

THE FINE STRUCTURE OF THE PURKINJE CELL

This paper describes the fine structure of the Purkinje cell of the rat cerebellum after fixation by perfusion with 1 per cent buffered osmium tetroxide. Structures described include a large Golgi apparatus, abundant Nissl substance, mitochondria, multivesicular bodies, osmiophilic granules, axodendritic and axosomatic synapses, the nucleus, the nucleolus, and the nucleolar body. A new and possibly unique relationship between mitochondria and subsurface cisterns is described. Possible functional correlations are discussed.