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  • 1
    ISSN: 1432-0495
    Source: Springer Online Journal Archives 1860-2000
    Topics: Geosciences
    Notes: Abstract Sediment samples of Ottawa River were examined using a relatively new technique, electron microscopy/energy dispersive (EM/ED) microanalyzer, to identify and document the binding sites for mercury on sediments and biota. Samples were deposited on a Nucleopore filter, dried, and then mounted on an aluminum stub for EM/ED analysis. Better images for documentation were obtained by depositing the samples directly on a carbon planchet, thus eliminating the insulation from the filter and the x-ray emmission from the aluminum stub. The salient features of ED x-ray microanalyzer, such as identification of most major and minor elements in a single analysis, and simple spectrum of x-ray energies versus atomic number of elements, are listed. Pitfalls in the methodology of the positive identification of elements resulting from peak shifting and peak overlap in the complex spectra of environmental samples are discussed. Remedies for successful resolution of broad spectra into individual elemental peaks are clearly outlined. Analyses of sediment samples revealed the presence of a variety of structures in aquatic environments with varying elemental compositions. Data gathered on mercury-bearing structures in the present study showed that mercury binding is on sulfur sites but never in a stoichiometric ratio; not all sulfur sites accumulated mercury. Possible reasons for sulfur sites void of mercury are (1) uneven distribution of binding sites, (2) concentrations of mercury too low to saturate all the binding sites, or (3) possible desorption of mercury from the binding sites by either chemical or biologic processes.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Microbial ecology 7 (1981), S. 183-193 
    ISSN: 1432-184X
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract The effects of brief exposure to, or growth in the presence of, lethal and sublethal concentrations of Cu(NO)2 and Cd(NO3) on the ultrastructure of the blue-green algaAnabaena 7120 and the green algaAnkistrodesmus braunii were studied. Exposure to increasing amount of both metal ions led to the appearance of larger proportions of electron-dense cells whose organelles were less well defined than those of untreated cells. Metal-treated cells ofAnabaena 7120 became distorted. Some had a corrugated appearance. Others lysed, leaving a much larger proportion of heterocysts. Such heterocysts were often empty or had a curious collapsed appearance. Growth ofA. braunii in the presence of 10−4 M Cu(NO2)2 produced substantial numbers of multinucleate giant cells with thick walls; such cells result from repeated mitotic division without subsequent cytokinesis. The giant cells contained centrioles, structures not as yet found in normal cells of the genusAnkistrodesmus. Some nuclei of giant, but not of normal, cells contained deep indentations that appeared as “holes” in cross section. Some giant cells also contained triple parallel strands of endoplasmic reticulum which extended across much of the cell, connecting to the nuclear envelope. Some ultrastructural changes were also noted in algal cells grown over sediment containing Cu or Cd, but these were generally less severe than those occurring when metal ions were added directly to the algal cultures.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Ultramicroscopy 13 (1984), S. 71-83 
    ISSN: 0304-3991
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Electrical Engineering, Measurement and Control Technology , Natural Sciences in General , Physics
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    International Journal of Insect Morphology and Embryology 5 (1976), S. 289-299 
    ISSN: 0020-7322
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Journal of Molecular Biology 165 (1983), S. 701-710 
    ISSN: 0022-2836
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Protoplasma 90 (1976), S. 139-154 
    ISSN: 1615-6102
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary The differentiation of resting cysts of the algaPolytomella agilis was examined by electron microscopy. During encystment the free-swimming, quadriflagellate unicells lose their flagella, sink to the bottom of the culture, and form a thick cell wall. Populations of cells at various stages of encystment were collected on microscope slides placed at the bottom of the culture flasks. The mature cyst wall consists of four layers which are laid down sequentially next to the plasma membrane. Freeze-etching has shown that the first layer of wall deposited consists of fibrils which are formed partly embedded within the plasma membrane. A proliferation of rough endoplasmic reticulum and Golgi bodies is seen in early stages of encystment followed by a reduction in size or number of these organelles and of plastids in the maturing cyst. Microtubular structures, including the basal bodies, dedifferentiate and are not observed in the later stages of encystment. The redifferentiation of the swimming cell during excystment is described in the companion paper.
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  • 7
    Electronic Resource
    Electronic Resource
    Springer
    Protoplasma 90 (1976), S. 155-171 
    ISSN: 1615-6102
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary Populations of mature resting cysts of the algaPolytomella agilis were purified from asynchronously encysting cultures and incubated in fresh culture medium to promote excystment. Up to 90 percent of the cysts germinated, with approximately 50 percent excysting between 3 and 7 hours of incubation. Each germinating cyst releases a single, fully differentiated, swimming cell. The entire excystment process of individual cysts was followed by light microscopy to establish the time course of release and cells at comparable stages of excystment were examined by electron microscopy. During the first 3 hours of incubation the cysts increase in size, presumably due to uptake of water, and a polarity is established in the cytoplasm which makes it possible to identify the site of subsequent release. Release involves a selective degradation of a portion of the cyst wall at this site followed by a physical rupturing of the weakened area. Details of the structural alterations in the wall and cytoplasm are described. The cytoplasmic organelles observed to dedifferentiate during encystment (preceding paper) are completely redifferentiated during excystment. The emergent cell is flagellated and possesses the elongate form typical of the swimming cell.
    Type of Medium: Electronic Resource
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  • 8
    ISSN: 1615-6102
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary In lakes, the non-living particulate and the colloidal organic component are usually much greater in mass than the living component. Electron microscopy reveals that electron-opaque, non-rigid fibrils of approximately 3 to 10 nm diameter are found abundantly on the surfaces of common lake algae and microbes, free in the water column and free on the surface of the lake bottom. Filtration experiments and some microscopical evidence indicate that these fibrils are readily lost by cells without concomitant cell damage. Individual fibrils may form complex meshlike aggregates which can break apart and reassociate. Meshlike aggregates also appear to adhere to cells and large suspended particles. The behaviour and contact relations of the fibrils and their aggregates suggest a role in contact cation exchange. This suggested role is bolstered by a composition of 20 to 30 percent uronic acid residues for washed samples from lake water. Water from axenic algal cultures and from lakes can be processed by a combination of filtration and centrifugation techniques to yield quantities of purified fibril preparations permitting chemical analyses. Initial analyses show some of their physical characteristics to be appropriate to the principal component of an hypothetical, organic, carrier system for the redistribution of bound but biologically available cations in lakes.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    [s.l.] : Nature Publishing Group
    Nature 317 (1985), S. 643-645 
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] Porin contains a large fraction of polar amino-acid residues1 and does not exhibit a single long hydrophobic stretch7. It is arranged predominantly in an anti-parallel /3-pleated sheet structure8. Though different from hydrophobic membrane proteins such as bacteriorhodopsin, a transmembrane ...
    Type of Medium: Electronic Resource
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  • 10
    Publication Date: 1989-08-01
    Print ISSN: 0027-8424
    Electronic ISSN: 1091-6490
    Topics: Biology , Medicine , Natural Sciences in General
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