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  • Scanning electron microscopy  (111)
  • Springer  (111)
  • American Geophysical Union
  • Blackwell Publishing Ltd
  • Cell Press
  • Institute of Physics
  • Nature Publishing Group
  • 2005-2009
  • 1975-1979  (77)
  • 1970-1974  (34)
  • 1935-1939
Collection
Keywords
Publisher
  • Springer  (111)
  • American Geophysical Union
  • Blackwell Publishing Ltd
  • Cell Press
  • Institute of Physics
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Years
Year
  • 1
    Electronic Resource
    Electronic Resource
    SEM analysis of amphibian mesodermal migration (1977)
    Springer
    Development genes and evolution 181 (1977), S. 31-40 
    Details
    ISSN: 1432-041X
    Keywords: Cell migration ; Mesoderm ; Gastrulation ; Scanning electron microscopy
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary At the end of gastrulation, the lateral mesoderm of amphibian embryos migrates ventrally between the ectoderm and the endoderm. The present study is an examination of the morphology of the leading cells of the mesodermal sheet and of the substratum over which they move (the inner surface of the ectoderm). The cells of the leading edge of the mesoderm are generally round, with very short and narrow flattened projections in the forward direction. These projections do not have a “ruffled” morphology, regardless of whether fixation is carried out before or after the ectoderm and mesoderm are dissected away from the endoderm. The inner surface of the ectoderm is covered with fine (450–500A) filamentous extracellular material and the ectoderm cells sometimes extend cytoplasmic processes (approx. 0.1 μ wide) onto the leading surface of the mesoderm or onto adjacent ectoderm cells. These studies indicate that the morphology of cell migration in amphibians is closer to that seen inFundulus than to that characteristic of chick or mammalian cells.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00857266
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  • 2
    Electronic Resource
    Electronic Resource
    Growth of embryonic chick tibiae in ovo and in vitro: A scanning electron microscope study (1979)
    Springer
    Calcified tissue international 27 (1979), S. 33-40 
    Details
    ISSN: 1432-0827
    Keywords: Chick embryo ; Bone ; Organ culture ; Scanning electron microscopy
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine , Physics
    Notes: Summary The study describes the ultrastructure of the mineralized portion of chick tibiae from 10 days in ovo to 2 days post-hatch. At 10 days a single mineralized cylinder surrounds the diaphysis. On its outer surface columnar trabeculae join to form ridges parallel to the long axis of the bone. These ridges are covered by another cylinder and form the haversian canals. At 11 days vascular invasion of the marrow cavity occurs and resorption of the endosteal surface begins. This type of periosteal deposition and endosteal resorption is repeated during and subsequent to embryonic development. The mineralized portion of 10-day chick tibiae cultured for 2 days in modified BGJ medium was compared with 10-, 11-, and 12-day tibiae in ovo. Cultured tibiae were similar in length and calcium content to 11-day tibiae in ovo. The form of mineral deposited in ovo and in culture was the same, namely, aggregates of spherical mineral clusters. Differences in culture included the following: (a) few concentric cylinders were deposited as compared with tibiae in ovo; (b) trabeculae were not arranged in rows and ridges in culture; (c) osteocytic lacunae were restricted to bases of trabeculae rather than uniformly distributed as in ovo; and (d) the endosteal surface of tibiae in culture appeared etched.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF02441158
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  • 3
    Electronic Resource
    Electronic Resource
    Correlation of freeze-fracture and scanning electron microscopy of epiphyseal chondrocytes (1978)
    Springer
    Calcified tissue international 26 (1978), S. 237-241 
    Details
    ISSN: 1432-0827
    Keywords: Epiphyseal chondrocytes ; Freezefracture ; Scanning electron microscopy ; Cell processes ; Membrane particles
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine , Physics
    Notes: Summary Chondrocytes in epiphyseal cartilage were examined by scanning electron microscopy (SEM) and transmission electron microscopy (TEM) using freeze-fracture techniques. Freeze-fracture replicas showed large numbers of fingerlike, 0.11–0.15 μm diameter, projections from the chondrocyte surface, with numerous 95–180 Å diameter intramembranous particles associated with both the cell membrane surface and these projections. With SEM, these cytoplasmic projections were also obvious, but appeared collapsed into clusters of globular-shaped projections on the surface of the chondrocytes. With freeze-fracture techniques, in which shrinkage artifacts were essentially eliminated, the cytoplasmic projections were often seen in intimate contact with the extracapsular matrix. However, with chondrocytes prepared by both SEM and conventional TEM, there was evidence of shrinkage, the cytoplasmic projections having little contact with the extracapsular matrix. These findings show that the cytoplasmic processes are not artifacts of tissue processing and provide morphological evidence in support of the hypothesis that matrix vesicles are of cellular origin.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF02013264
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  • 4
    Electronic Resource
    Electronic Resource
    Scanning electron microscopical study on the fluorosis of enamel in rats (1978)
    Springer
    Calcified tissue international 25 (1978), S. 75-83 
    Details
    ISSN: 1432-0827
    Keywords: Rat ; Fluorosis ; Enamel ; Scanning electron microscopy ; Low temperature incineration
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine , Physics
    Notes: Summary Sixteen 58-day-old male rats of Wistar strain, with a mean body weight of 179 g, were divided into two equal groups. Each group of eight animals was maintained for 70 days on drinking water, ad lib., containing no fluorine (control group) and 100 ppm of fluorine (experimental group). All specimens examined were obtained from the incisal portions of the incisors. The following types of enamel specimens were prepared for scanning electron microscopy: (1) acid-etched specimens; (2) acid-etched specimens followed by low temperature microincineration; and (3) fractured specimens. The enamel formed during high fluoride exposure showed marked hypocalcification, that is, the crystallite density in the prism core and interprismatic region was lower than that of control animals. The organic substances appeared to increase in these regions. These changes were prominent in the outer and middle enamel layers. Such changes following fluoride administration appear to indicate an inhibition of enamel maturation, that is, an inhibition of the mineral deposition and/or an inhibition of organic matrix withdrawal.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF02010754
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  • 5
    Electronic Resource
    Electronic Resource
    Structure and association of wall fibrils produced by regenerating tobacco protoplasts (1979)
    Springer
    Planta 146 (1979), S. 203-210 
    Details
    ISSN: 1432-2048
    Keywords: Cellulose ; Microfibrils ; Negative staining ; Nicotiana ; Protoplasts ; Scanning electron microscopy
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract A study has been made of the wall fibrils produced by tobacco protoplasts, using scanning electron microscopy in conjunction with negative staining. It has been shown that the fibres seen in scanning electron microscopy correspond to aggregates of microfibrils. These aggregates are only visible where they are lifted clear of the protoplast surface. Negative staining of fixed protoplasts shows that the aggregation of microfibrils into the fibres visible in scanning electron microscopy is probably produced by air-drying. Gentle disruption of microfibrils produces both random broken fragments and bundles of short pieces of fibrillar material about 60 nm in length. This material is present in undisrupted young walls, but not in undisrupted older walls. The microfibrils in young walls seem much more fragile and liable to breakage than those in older walls. These results are discussed in terms of the interpretation of scanning electron microscope images and the mechanism of cellulose microfibril formation by higher plants.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00388233
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  • 6
    Electronic Resource
    Electronic Resource
    Localization of α-galactomannan on the surface of Schizosaccharomyces pombe cells by scanning electron microscopy (1977)
    Springer
    Archives of microbiology 112 (1977), S. 123-126 
    Details
    ISSN: 1432-072X
    Keywords: Bandeiraea simplicifolia ; Schizosaccharomyces pombe ; Colloidal gold ; Cytochemistry ; α-Galactomannan-lectin ; Scanning electron microscopy
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Galactomannan was localized by scanning and transmission electron microscopy on the cells and cell walls of Schizosaccharomyces pombe. The markers were prepared from colloidal gold granules labelled with an α-galactopyranosyl-binding lectin isolated from the seeds of Bandeiraea simplicifolia. Part or all of this α-galactomannan was present in the outer layer of the cell wall and was uniformly distributed even on the fission scars.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00429323
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  • 7
    Electronic Resource
    Electronic Resource
    Localization of mannan at the surface of yeast protoplasts by scanning electron microscopy (1976)
    Springer
    Archives of microbiology 109 (1976), S. 9-14 
    Details
    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.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00425106
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  • 8
    Electronic Resource
    Electronic Resource
    Mating in Chlamydomonas eugametos (1976)
    Springer
    Archives of microbiology 109 (1976), S. 31-35 
    Details
    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.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00425109
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  • 9
    Electronic Resource
    Electronic Resource
    Scanning electron microscopic studies on the synaptic bodies in the rat retina (1970)
    Springer
    Cell & tissue research 107 (1970), S. 45-53 
    Details
    ISSN: 1432-0878
    Keywords: Retina ; Rat synaptic bodies ; Synaptic ribbon ; Extracellular material ; Scanning electron microscopy
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary The ultrastructure of the synaptic bodies in the outer and inner plexiform layers of the rat retina was studied with scanning and transmission electron microscopy. The synaptic bodies in the outer plexiform layer are pear-shaped and their vitreal pole invaginated by processes from nerve cells. Their surfaces are covered with extracellular material, which is partly dissolved or redistributed during the fixation and rinsing procedure. The internal structure of the synaptic bodies is described. The synaptic bodies in the inner retinal plexiform layer are more difficult to identify with the scanning electron microscope. They are polyhedronal and also covered with extracellular material. The observations are discussed. The value of the application of two different preparation and analyzing methods, i. e. the scanning and the transmission electron microscopy, is stressed.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00338957
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  • 10
    Electronic Resource
    Electronic Resource
    Die morphologische Differenzierung des visceralen Blattes der Bowmanschen Kapsel (1970)
    Springer
    Cell & tissue research 111 (1970), S. 346-363 
    Details
    ISSN: 1432-0878
    Keywords: Kidney ; Glomerulus ; Development ; Scanning electron microscopy
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Description / Table of Contents: Zusammenfassung Die Differenzierung der Podocyten wurde an Nieren 10 Tage alter Ratten raster-elektronenmikroskopisch untersucht und mit durchstrahlungs-elektronenmikroskopischen Befunden verglichen. Die Podocytenfortsätze können danach auf dreierlei Wegen gebildet werden: 1. Spalten innerhalb des Cytoplasmas lassen bandartige Cytoplasmabrücken entstehen. Diese gliedern sich weiter auf, bis zahlreiche miteinander verzahnte Fortsätze derselben Zelle entstanden sind. 2. Vom Zellrand her werden dicke Fortsätze weit vorgeschoben, die kleinere Fortsätze bilden. Durch sie können Verzahnungen mit entfernten Deckzellen entstehen. Die kleinen Fortsätze können sich jedoch auch mit anderen Fortsätzen der eigenen Zelle verzahnen. 3. Fingerförmige Fortsätze benachbarter Zellen verzahnen sich während ihrer Entstehung miteinander. Trotz zahlreicher desmosomenartiger Haftstellen zwischen benachbarten Podocyten entwickeln sich ihre Fortsätze und deren Verzahnungen anscheinend weitgehend autonom und nur selten nach den vermuteten Regeln epithelialer Nachbarschaft (Typ 3). Die Befunde sprechen vielmehr dafür, daß durchflutete und wachsende Glomerulumkapillaren die Podocytendifferenzierung induzieren und die Orientierung der Fortsätze beeinflussen.
    Notes: Summary The differentiation of the podocytes was studied by scanning electron microscopy on kidneys of 10 days old rats. The results were compared with transmission electron microscopic pictures from the same kidneys. There are three ways of forming processes by the podocytes: 1. Slits within the cytoplasm give rise to cytoplasmic bridges which further divide themselves and finally build up a meshwork of processes within a cell. 2. Thick and sometimes very long processes originate from the cell border. Their smaller branches may interdigitate with those of distant podocytes or with other processes out of the same cell. 3. Finger-like processes of neighbouring cells interdigitate as soon as they develop. In spite of numerous desmosomal structures between neighbouring podocytes the cell processes and their interdigitations develop mostly independently from each other and only seldom after the expected rules of epithelial vicinity (type 3). These findings are interpreted as indication that flooded and growing capillaries induce the differentiation of podocytes and that they influence the orientation of their processes.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00342487
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