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  • Scanning electron microscopy  (27)
  • Springer  (27)
  • Cambridge University Press
  • National Academy of Sciences
  • Nature Publishing Group
  • 1980-1984  (11)
  • 1975-1979  (16)
  • 1981  (11)
  • 1976  (16)
Collection
Publisher
  • Springer  (27)
  • Cambridge University Press
  • National Academy of Sciences
  • Nature Publishing Group
Years
  • 1980-1984  (11)
  • 1975-1979  (16)
Year
  • 1
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    Springer
    Archives of microbiology 130 (1981), S. 189-194 
    ISSN: 1432-072X
    Keywords: Fuligo septica ; Myxomycetes, mycetozoans ; Acellular slime molds ; True slime molds ; Spore germination ; Swarm cell morphogenesis ; Scanning electron microscopy
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract This report describes conditions under which spores of the acellular slime mold Fuligo septica underwent a very rapid, synchronous and complete (100%) germination followed by morphogenesis of motile, flagellated swarm cells from the released protoplasts. This developmental sequence was initiated immediately upon wetting the spores with a surfactant and was completed within 40–50 min in the absence of any exogenous nutrient other than sodium phosphate buffer. Oxygen was required for germination. The rate and percentage of germination diminished with increasing spore concentration suggesting the existence of an autoinhibitor. The morphological sequence of events in the differentiation process was examined by scanning electron microscopy.
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  • 2
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    Archives of microbiology 130 (1981), S. 307-311 
    ISSN: 1432-072X
    Keywords: Paracoccus denitrificans ; Cell surface ; Outer membrane ; Lysozyme ; Scanning electron microscopy ; NaCl treatment
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract The effects of water washing and NaCl treatment on the cell surface of P. denitrificans were studied. Both treatments caused a release of material from cells. Chemical studies showed that NaCl treatment released material containing components characteristic of outer membrane. This treatment also increased the susceptibility of the organism to lysozyme. Scanning electron microscopy was used to monitor the effects of water washing and NaCl treatment on the cell surface. Both treatments were shown to alter the appearance of the cell surface. The disruptive effects of these procedures were found to be dependent upon the age of the culture.
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  • 3
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    Archives of microbiology 109 (1976), S. 9-14 
    ISSN: 1432-072X
    Keywords: Candida utilis ; Saccharomyces cerevisiae ; Colloidal gold ; Cytochemistry ; Mannan ; Plasma membranes ; Scanning electron microscopy
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract The β(1→3)glucanase of Basidiomycete QM 806 was used to prepare Saccharomyces cerevisiae and Candida utilis protoplasts. Plasma membranes isolated from S. cerevisiae contained a small amount of mannose and traces of glucose and ribose. Randomly distributed α-mannan was detected by scanning electron microscopy at the surface of prefixed protoplasts using colloidal gold labelled with Concanavalin A as a marker. C. utilis protoplasts were also marked with anti-mannan antibodies. Again the distribution of mannan was random. This experiment indicated also that plasma membrane mannan has the same immunochemical determinants as cell wall mannan. It is hypothesized that mannan is mainly located in the outer layer of plasma membranes.
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  • 4
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    Archives of microbiology 109 (1976), S. 31-35 
    ISSN: 1432-072X
    Keywords: Scanning electron microscopy ; Chlamydomonas ; Cell agglutination ; Cell fusion ; Flagella
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract A technique has been developed by which mating gametes of Chlamydomonas eugametos can be studied in the Scanning Electron Microscope. A detailed description of the mating process, from the initial flagellar agglutination until the release of free vis-à-vis pairs, is presented. Flagella appear to agglutinate at random points on their surface. This is followed by a rapid increase of the contact area such that they “line-up” tip to tip. Flagella always exhibit a typical position prior to cell fusion. After cell fusion the flagella of a pair separate rapidly while the female have shortened about 33%. In a vis-à-vis pair the plasma bridge has contracted. The observations are interpreted in terms of a specific reorganization of the sexuale aggregate.
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  • 5
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    Cell & tissue research 170 (1976), S. 145-159 
    ISSN: 1432-0878
    Keywords: Neurogenesis ; Retina ; Scanning electron microscopy
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary Fixed retinae of chick embryos and chicks of the first week after hatching were fractured and examined with the scanning electron microscope. The matrix cells of the retina proliferate up to the beginning of the second week. The migrating cells are oriented in cell cords. This columnar organization prevails up to the development of the plexiform layers formed as a consequence of the outgrowth of the dendritic and axonal cell processes. Special attention was paid to the differentiation of the ganglion, bipolar and receptor cells, and the radial fibers (Müller cells). Two main morphological patterns are significant for the organization of the retina during neurogenesis: a) the cell to cell contacts of migrating cells and b) the spatial arrangement of Müller cells which could provide guidelines for migration of neuronal elements.
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  • 6
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    Cell & tissue research 174 (1976), S. 129-137 
    ISSN: 1432-0878
    Keywords: Pineal organ, human ; Acervuli ; Scanning electron microscopy ; Transmission electron microscopy ; Electron probe microanalysis
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary Untreated, decalcified and trypsinized acervuli from human pineal bodies were studied with the scanning and transmission electron microscope as well as by electron probe microanalysis. The mulberry-like acervuli are composed of a various number of spherical lobes (135–800 μm) between which clustered groups of globuli (4–14 urn in diameter) are observed. The acervular lobes are very probably formed by an aggregation of these globuli. Small round particles 125–500 Å in diameter are observed on the surface of the pineal concretions. These are not influenced by either decalcification or trypsin treatment. The acervular mineral corresponds morphologically to hydroxyapatite. The electron probe microanalysis reveals the existence of calcium and phosphorus as main components of the acervuli. Small quantities of magnesium and strontium were also detected.
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  • 7
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    Cell & tissue research 170 (1976), S. 1-16 
    ISSN: 1432-0878
    Keywords: Tissue culture cells ; Mycoplasma ; Light microscopy ; Transmission electron microscopy ; Scanning electron microscopy ; Morphometry
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary The host-parasite relationship of HeLa M cells artificially infected with a bovine species of Mycoplasma was studied by light microscopy, transmission electron microscopy and scanning electron microscopy. The use of morphometry to quantitate some of the findings was explored. The parasites were seen in locations extracellular to the cell surface. The detection of small numbers of organisms by light microscopy was well demonstrated by use of the fluorescent antibody technique. Scanning electron microscopy proved to be an excellent method for revealing the surface details of cell-parasite morphology. Ultra-thin sections showed that the parasites are aligned mostly parallel to the plasma membrane of the host cell but separated by a gap of 10 nm. Morphometry indicated an average of 69 organisms per cell surface occupying 1.7% of the surface area. An increase of 26% in diameter of the HeLa cells, possibly as a result of infection, was observed.
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  • 8
    ISSN: 1432-0878
    Keywords: Axons ; Scanning electron microscopy ; Neurones, afferent ; Nerve regeneration ; Spinal nerve roots
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary Rat dorsal spinal nerve roots were cut and the tip on the ganglionic side of the cut was examined by scanning electron microscopy at 0, 7, 20 and 48 h after operation. Seven hours after cutting, free axonal sprouts had started to protrude from the cut end of the nerve. After 20 h the free sprouts were more profuse than at 7 h but were smaller and had a rougher surface. At both 7 and 20 h many of the sprouts consisted of a stalk 2–7 μm in diameter with a bulbous end 5–20 μm in diameter. A few branching sprouts were seen. At 48 h the sprouts were shrunken with a deeply furrowed surface. The significance of the surface structure of the sprouts is discussed.
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  • 9
    ISSN: 1432-0878
    Keywords: Epididymal epithelium ; Castration ; Androgen-substitution ; Japanese monkey ; Scanning electron microscopy
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary The caput epididymidis from castrated and androgen-supplemented, castrated Japanese monkeys was observed with the scanning electron microscope. The experimental findings were compared with the normal structures in control animals. The epididymal lumen of control animals was lined by a tall, pseudostratified columnar epithelium possessing long, slender stereocilia which were densely arranged in a tuft-like form. After castration, the epididymal epithelium was decreased in height to one-fifth of controls. The stereocilia were also considerably reduced in length and in number, resulting in a flattened epithelial surface with polygonal boundaries. Frequent projection of a long, single cilium from an epithelial cell into the lumen was also a prominent feature in the epididymal ducts of the castrated animals. Administration of testosterone to the castrated animals resulted in almost complete recovery of the epididymal epithelium as well as regeneration of the stereocilia which regained a tuft-like arrangement.
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  • 10
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    Cell & tissue research 172 (1976), S. 379-388 
    ISSN: 1432-0878
    Keywords: Chitons ; Receptors ; Shell surface ; Scanning electron microscopy
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary The shells of the chitons Lepidochitona cinereus, Sypharochiton pelliserpentis, Amaurochiton glaucus and Onithochiton neglectus were examined by scanning electron microscopy. In all species the surface terminations of the megalaesthete and micraesthete organs could be identified lying flush with the shell surface, as well as, lenses of the shell eyes in O. neglectus. Periostracal debris and encrusting diatoms were a usual feature of the shell surfaces. The micraesthete subsidiary caps normally appear featureless, but the megalaesthete apical caps sometimes appear to be perforated. The reasons for this perforate appearance are discussed and it is concluded that it provides no evidence for the normal passage of substances out of or into the megalaesthete.
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  • 11
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    Cell & tissue research 166 (1976), S. 65-70 
    ISSN: 1432-0878
    Keywords: Collagen ; Bone ; Cell culture ; Scanning electron microscopy
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary Embryonic and young rat bone cells have been grown in culture and examined in the scanning electron microscope (SEM). Compared with cells fixed in situ and taken directly from the animal, the cultured osteoblastic cells were smoother, flatter and more extensive and showed tighter intercellular contacts. Some matrix is formed in culture and undergoes at least partial mineralization as judged by the accumulation of Ca and P measured by energy dispersive x-ray analysis. Findings concerning the morphology of the collagen arrangement were indecisive. Some superficial cells, free of surrounding matrix, resembled osteocytes in normal in vivo bone. This may indicate that a proportion of the extracellular matrix produced by the cultured cells failed to polymerise into recognizable bone matrix, and that osteocytic morphology is not dependent upon the physical characteristics of the bone matrix.
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  • 12
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    Cell & tissue research 169 (1976), S. 277-287 
    ISSN: 1432-0878
    Keywords: Rabbit gametes ; Cryofractography ; Scanning electron microscopy ; Transmission electron microscopy ; Zona pellucida
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary Rabbit ova fertilized in vitro were prepared for scanning electron microscopy by ethanol-cryofracturing and critical-point drying methods and were also embedded and sectioned for transmission electron microscopy. Study of a region of interaction between sperm and zona pellucida with scanning electron microscopy reveals the latter to be composed of a complex network of fibers interspersed with numerous pores. Transmission electron microscopy of the same region reveals a “typical” homogeneous composition of the zona pellucida. Ultrastructural observations of thin sections passing through the region of sperm-egg interactions or through other regions of the ovum or its investments reveals very little methodological distortion of the various intracellular organelles or matrix. Application of the procedures described provides not only an elucidation of surface detail but also reveals intracellular cytoplasmic information about the same specimen during in vitro fertilization.
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  • 13
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    Cell & tissue research 169 (1976), S. 449-465 
    ISSN: 1432-0878
    Keywords: Bone ; Osteoblasts ; Cell surface ; Cell shape ; Calcitonin ; Parathyroid extract ; Scanning electron microscopy
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary Neonate rat endocranial osteoblasts were cultured on their bone surfaces in control medium (CC) or medium to which either parathyroid extract (PTE) or calcitonin (CT) had been added for 2, 4, 8 or 24 h. Some were cultured for 24 h in CC, then for 2, 4, 8 or 24 h in either CT or PTE medium; or for 24 h in PTE, then for 2, 4, 8 or 24 h in either CC or CT; or 24 h in CT and 2, 4, 8 or 24 h in CC. The dorsal ruffling of the cells in CC was found to be suppressed by later culturing with PTE and the disoriented cells reorganized to form arrays of parallel cells. The effects of PTE were also reversed by CC or CT: the osteoblasts in the second culture (CC) lost elongation and order, and proceeded through a proliferative phase before exhibiting the ruffling form similar to a single CC 24 h culture. PTE-cultured osteoblasts showed an increase in cell overlap and contact so that a more competent barrier was formed separating the bone from the medium. In control or CT medium, however, intercellular gaps were greater than in vivo.
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  • 14
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    Cell & tissue research 166 (1976), S. 91-100 
    ISSN: 1432-0878
    Keywords: Kidney (rat) ; Uriniferous tubule ; Scanning electron microscopy
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary The fine structure of luminal surface of clearly identified portions of uriniferous tubules has been studied by scanning electron microscopy to elucidate some controversies concerning the topography of certain surface formations. The results show a characteristic pattern of the luminal surface in the region of Henle's loop, which was assumed by previous authors, to belong to the collecting tubule. Furthermore it is demonstrated that no cilia are present within the terminal portion of the collecting tubules.
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  • 15
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    Cell & tissue research 174 (1976), S. 499-518 
    ISSN: 1432-0878
    Keywords: Fibroblast ; Human ; Transmission electron microscopy ; Scanning electron microscopy ; Aggregation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary The different stages during aggregation of diploid human skin fibroblasts have been examined by transmission and scanning electron microscopy. As a result of aggregation, fibroblasts form a complex tissue configuration. Numerous intercellular junctions can be observed, while the cells remain polygonal and do not develop an organised intracellular cytoskeleton. Cell division occurs only rarely. After aggregation, signs of progressive auto-digestion develop. Adhesion to a substrate results in outgrowth of the cells and monolayer formation, even when extensive cell damage had occurred. The morphology of fibroblasts in aggregates and in the monolayers, from which they were derived, is compared and the contribution of the aggregate system to the study of fibroblast behavior is discussed.
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  • 16
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    Cell & tissue research 166 (1976), S. 299-314 
    ISSN: 1432-0878
    Keywords: Renal glomerulus (Rat) ; Endothelial cells ; Blood capillaries ; Scanning electron microscopy
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary The rat kidney was perfused with saline and glutaraldehyde, treated with Murakami's tannin-osmium impregnation method, ethanol-freeze cracked and dried by the critical point method. Gold-palladium evaporated specimens were observed in a field-emission scanning electron microscope. The glomerular filtration membrane, fractured in different planes was observed with the following results: 1. Adjacent pedicles originate from different podocytes. No interpedicular bridges of apparent cytoplasmic nature could be found. 2. The basement membrane, in grazing fractures shows a horizontally layered architecture. 3. The attenuated endothelial sheet (lamina fenestrata) is divided into compartments, which we suggest should be called “areolae fenestratae”, by cytoplasmic crests radiating from the nucleated portion of the endothelial cell. A crest also occurs along the cell margin, which contacts a similar crest at the margin of the adjacent cell. 4. The pores in the areolae fenestratae are variable in size (30−150 nm diameter). A knob-like projection from the apparently naked basement membrane is found in a portion of the pores. 5. Numerous microvilli may occur on the endothelium. Some of them anastomose and fuse with one another to form a net whose meshes appear identical with the endothelial pores. Domes and shelves formed of a fenestrated cytoplasmic sheet also occur above the ordinary level of the endothelial lining. A hypothesis implicating microvilli in partial renewal of the endothelial sheet is proposed. This study was assisted by Mr. K. Adachi of the SEM Laboratory at the Niigata University School of Medicine.
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  • 17
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    Cell & tissue research 167 (1976), S. 425-438 
    ISSN: 1432-0878
    Keywords: Scanning electron microscopy ; Crystalline lens ; Microphthalmos
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary The surface features of cortical fibers from lenses of normal adult rats and microphthalmic rats of the Browman strain have been studied by scanning electron microscopy. In the normal lenses, superficial cortical fibers follow a straight course from inner to outer pole whereas the deeper cortical fibers, while straight near the poles, pursue an undulating or zig-zag course at and near the equator. Almost all of the fibers are hexagonal in cross section and all fibers throughout their entire length are bound by interdigitating processes at each corner of the hexagon to corners of two adjacent fibers. Some fibers are also affixed by a single row of ball and socket junctions located on their broad outer and inner surfaces. Lens fibers from Browman rats display both minor and major abnormalities. These included segmentation, formation of incisures and lateral protrusions, corrugation and villous-like alteration of the broad fiber surface and development of parallel ridges on broad surfaces in a basket-weave pattern.
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  • 18
    ISSN: 1432-0878
    Keywords: Retina ; Haplochromis burtoni ; Photoreceptor cells ; Light-adaption, dark-adaption ; Scanning electron microscopy
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary The photoreceptor layer in the retina of Haplochromis burtoni (Cichlidae, Teleostei) was studied by scanning electron microscopy. Three types of receptors were identified: rods, single-cones and double-cones. The three-dimensional arrangement of these photoreceptors is described in the light- and dark-adapted retina. The surface of the inner segment of the photoreceptor cells displays fine vertical fissures which give rise to slender processes. These so called calycal processes which are of different lengths in rods and cones, surround the beginning of the smooth-surfaced outer segment. The myoid, the contractile part of the receptor, which is located beneath the ellipsoid, was examined in the single-cones of the dark-adapted retina. It is a slender structure with surface infoldings. The myoid, studied by transmission electron microscopy, contains bundles of parallel myofilaments, which are thought to be contractile.
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  • 19
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    Cell & tissue research 216 (1981), S. 647-654 
    ISSN: 1432-0878
    Keywords: Mast cells ; Regeneration ; Exocytosis ; Scanning electron microscopy
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary Cell-surface morphology of regenerating mast cells was followed over a period of 48 h after histamine release. Control cells (not stimulated to secrete) were characterized by anastomosing folds of membrane of equal depth and width. During exocytosis these folds disappeared and were replaced by deep cup-shaped flaps of membrane evident in cells incubated for 10 min. During the first hours of regeneration these flaps fused mutually or with the plasma membrane. This activity suggests membrane retrieval, maybe specifically recycling the granule-type patches of membrane. Membrane-fusion activity was observed to some degree also after extended incubation. After 48 h of incubation the regeneration process was still not completed, as indicated by the fact that holes leading to intracellular cavities could still be found.
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  • 20
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    Colloid & polymer science 259 (1981), S. 252-259 
    ISSN: 1435-1536
    Keywords: Scanning electron microscopy ; polyethylene ; microfibrillar structure ; lamellar structure ; drawing mechanism
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Description / Table of Contents: Zusammenfassung Die mikrofibrillare und lamellare Morphologie in kaltverstreckten bzw. kaltverstreckten und anschließend getemperten HD-Polyäthylenplatten wurden mittels Raster-Elektronenmikroskopie untersucht. Kontrastunterschiede an Bruchoberflächen im Falle kaltverstreckten Polyäthylens werden interpretiert durch eine, vom Verstreckmechanismus bedingte, bevorzugte Orientierung der inter-mikrofibrillaren tie-Moleküle in der Plattenebene. An kaltverstreckten/getemperten Platten wurden Lamellenstapel beobachtet, die eine Zwillingsorientierung von geneigten Lamellen aufwiesen. Diese ‚dachförmige’ Struktur wird erzeugt durch eine Scherung innerhalb der Mikrofibrillen während der Mikro-Halsbildung und deutet das bekannte 4-Punkt-Röntgen-Kleiriwinkelbeugungsdiagramm. Zur Auflösung der einzelnen, lamellaren Textur wurde eine leichte Ätzung mit rauchender Salpetersäure benötigt.
    Notes: Summary The microfibrillar and lamellar morphologies in cold-drawn and cold-drawn/annealed high-density polyethylene sheets were observed by means of scanning electron microscopy. Differences in contrast on fracture surfaces for cold-drawn sheet are interpreted in terms of a preferential orientation of inter-microfibrillar tie molecules in the plane of the sheet brought about by the drawing mechanism. In annealed, cold-drawn sheet, stacks of lamellae were observed which showed twinned orientations of inclined lamellae. This “roof-top” structure is interpreted in terms of shear within the individual microfibrils during micronecking, and corresponds to the well-known 4-point small-angle X-ray pattern for this type of specimen. Light etching with fuming nitric acid was necessary in order to resolve the individual lamellar texture.
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  • 21
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    Cell & tissue research 215 (1981), S. 171-179 
    ISSN: 1432-0878
    Keywords: Polychaeta, Serpulidae ; Gamete ; Larva ; Development ; Scanning electron microscopy
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary Gametes and developing larvae of the polychaete Galeolaria caespitosa were examined by scanning electron microscopy. The sperm display a primitive morphology. When treated with 0.33 M CaCl2, they release a branched acrosomal process. At spawning, the polygonal oocytes have a granular surface made up of spherules and the tips of microvilli. The oocyte coat develops a ridged appearance as the oocyte rounds up. At fertilization, the microvilli are withdrawn from the coat surface. Microvilli again appear on the coat surface during the trochophore stage, but the egg coat appears to be retained as the larval cuticle until the demersal stage. The surface of the larva now shows many microvilli. Details of the organization of several ciliary structures are clarified. Moreover, the present study shows rapid, sequential development of paired setal sacs, with the most anterior pair appearing first.
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  • 22
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    Cell & tissue research 215 (1981), S. 193-205 
    ISSN: 1432-0878
    Keywords: Scanning electron microscopy ; Monkey liver ; Sinusoids ; Kupffer cells
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Description / Table of Contents: Zusammenfassung An der Affenleber wurden die verschiedenen Gefäßabschnitte des Leberläppchens mit dem Raster- und Transmissionselektronenmikroskop untersucht. Die Gefäßwände der portalen und terminalen (Zentral-) Venen werden durch ein geschlossenes Endothel, eine kontinuierliche Basalmembran und eine Bindegewebsschicht gebildet. Dagegen haben Sinusoide ein Endothel mit typischen Fenestrationen, wobei eine Basalmembran fehlt und nur ein schütteres Netz von Bindegewebsfasern im Disse'schen Raum vorkommt. Kupffer-Zellen findet man in den Sinusoiden, den terminalen Lebervenen und den Sublobularvenen; in Portalvenen kommen sie nicht vor. Ihre bezeichnenden Strukturen sind eine Oberflächenfältelung und besondere Zellfortsätze, Filopodien und Lamellipodien, mit denen sie am Endothel anhaften oder mit denen sie untereinander in Verbindung stehen. Im Disseschen Raum kommen flache Zellfortsätze von Fettspeicherzellen vor, die das Endothel umgeben. Es wird angenommen, daß sie eine perizytenähnliche Funktion haben.
    Notes: Summary The vasculature of the hepatic lobule of the monkey was investigated by scanning and transmision electron microscopy. The vessel walls of the portal and terminal hepatic (central) veins consist of a closed endothelium, a continuous basement membrane and a connective tissue layer. Sinusoids, however, show endothelia with typical fenestrations, and connective tissue fibres are only sparsely distributed in the space of Disse. Kupffer cells are present in the sinusoids, and occasionally in the terminal hepatic and sublobular veins, but are never present in the portal veins. They are characterized by a ruffled surface and special processes — filopodia and lamellipodia — which anchor them to the endothelial cells and also connect them with adjacent Kupffer cells. Flat branches of perisinusoidal cells, which encircle the endothelia, occur in the space of Disse, and are presumed to have a pericyte-like function.
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  • 23
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    Cell & tissue research 218 (1981), S. 403-420 
    ISSN: 1432-0878
    Keywords: Brush cells ; Common bile duct ; Thin section ; Freeze-fracture ; Scanning electron microscopy
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary Two different fixative procedures (immersion and perfusion) and four different fixative solutions were used in order to obtain the best preservation of the brush cells of the common bile duct of the rat. The results indicate that only perfusion fixation through the common bile duct is suitable, independent of the fixative solutions and their osmolarity. Numerous brush cells were seen in the proximal and distal regions of the common bile duct. In these locations, they could be implicated in a registration and/or regulation of intraluminal pressure variations.
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  • 24
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    Cell & tissue research 219 (1981), S. 297-311 
    ISSN: 1432-0878
    Keywords: Choroid plexus (chick) ; Third ventricle ; Ependyma ; Development ; Scanning electron microscopy
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary The surface morphology of the diencephalic choroid plexus (Pl. ch. v. III) was investigated by light microscopy and scanning electron microscopy in chicks from the 7th embryonic day (ED) to the 8th week after hatching. Pl. ch. v. III develops on the anterior ventricular roof from a sagittally oriented fold and a few posteriorly located transverse folds. On the 7th ED no significant differences in the cell surface morphology between Pl. ch. v. III and the surrounding ependyma are observed: both are covered with cilia. During the next four days, long cell prolongations (one per cell) covered with microvilli develop first on the surface of the posterior ventricular roof and then on the posterior part of Pl. ch. v. III. These structures are transitory. On the 11th ED, round cell prolongations (one per cell) appear progressively on the entire plexus, also replacing the long ones. Now the plexus surface is distinct from the surface of the surrounding ependyma. During the last week before hatching and also after hatching, the round cell prolongations become less prominent. Simultaneously, the number of cilia per unit surface area diminishes. With consideration of earlier reports, this study suggests that the following factors are involved in the increase of the surface area of Pl. ch. v. III: (I) The pseudostratified epithelium changes into columnar epithelium. (2) Ependymal elements of the posterior roof of the 3rd ventricle contribute to the anlage of Pl. ch. v. III. In later stages, however, Pl. ch. v. III grows only by mitoses.
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  • 25
    Electronic Resource
    Electronic Resource
    Springer
    Cell & tissue research 215 (1981), S. 515-529 
    ISSN: 1432-0878
    Keywords: Pituitary ; Rathke's cleft ; Ultrastructure ; Scanning electron microscopy ; Rat
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary SEM reveals that the inner surface of the pituitary cleft is lined by a continuous layer of marginal cells possessing microvillous and ciliated apical surfaces. The ciliated cells are more numerous on the posterior side (toward the pars intermedia) than on the anterior side of the cleft (toward the pars distalis). In contrast small infoldings (crypts) were occasionally noted only on the marginal layer covering the distal part of the hypophysis. In some areas of the cleft the surface features of the marginal cells are rather similar to the epithelial cells populating the upper parts of the respiratory tract in their topography and distribution. In other regions they also show striking similarities with the ependymal cells (tanycytes) lining the lateral recesses of the 3rd ventricle and the infundibular process with which the pituitary cleft has a very close topographical relationship. The parenchymal cells of the pars distalis are closely related to the flattened marginal cells of the cleft. The intercellular spaces of the pars distalis form a three-dimensional labyrinthic series of cavities continuous with the submarginal spaces of the cleft. Further SEM and TEM results demonstrate that the majority of the microvillous marginal cells lining both sides of the cleft possess surface features such as bulbous protrusions, laminar evaginations and large cytoplasmatic vacuoles, which are very likely the expression of an active transport of fluids. On the basis of these results it is concluded that the fluid-like material (colloid) present in the pituitary cleft is mainly derived from the fluids contained in the lacunar spaces of the pars distalis. Thus, marginal cells by absorbing fluids from the cleft by active endocytosis, may transport to the pars intermedia material (or hormones) produced in the distal part of the gland and vice versa. The cilia present on many marginal cells, based on their 9+2 tubular pattern, possess a kynetic role. This is very similar to that shown by the ciliated cells of the ependyma lining the brain ventricles. The occurrence of ciliated cells within the pituitary parenchyma (mainly in the follicles) suggests that they probably arise from the ciliated cells populating the marginal layer of the cleft and with which the parenchyma cells are closely related.
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  • 26
    Electronic Resource
    Electronic Resource
    Springer
    Cell & tissue research 217 (1981), S. 599-610 
    ISSN: 1432-0878
    Keywords: Ciliated peritoneal funnels ; Toad ; Scanning electron microscopy
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary Scanning electron microscopy revealed 600–800 ciliated peritoneal funnels opening onto the ventral surface of each kidney in Bufo marinus. The size and configuration of funnel apertures vary greatly, but individual funnels do not appear to change their dimensions. The peritoneal funnels course beneath the kidney surface before opening into peritubular blood vessels. Injections of India ink into the peritoneal cavity demonstrate that cilia lining the peritoneal funnels create a current carrying peritoneal fluid into the renal vasculature. Clearance of fluid by the funnels was dependent on pressure in the peritubular vessels, and was increased by arginine vasotocin. Ciliated peritoneal funnels may provide an important route for return of lymphatic fluid from the peritoneal cavity to the vasculature.
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  • 27
    Electronic Resource
    Electronic Resource
    Springer
    Cell & tissue research 219 (1981), S. 659-663 
    ISSN: 1432-0878
    Keywords: Gossypol ; Spermatozoa ; Contraception ; Cytoplasmic droplet ; Scanning electron microscopy
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary Spermatozoa from the cauda epididymidis of gossypol-treated rats exhibit distinctive departures from the morphology of spermatozoa from control rats: wrinkled and disorganized cell membrane in the head and tail regions, cell membrane missing from segments of the tail midpiece and principal piece regions, malformed heads, decapitate spermatozoa, retention of a cytoplasmic droplet at variable loci along tail midpieces, and looped tails. The observations suggest that gossypol exerts its contraceptive effect during spermatocytogenesis and spermiogenesis, including the posttesticular development and maturation of spermatozoa in the epididymis.
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