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  • 1
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Physica C: Superconductivity and its applications 153-155 (1988), S. 1523-1524 
    ISSN: 0921-4534
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Physics
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Physica C: Superconductivity and its applications 153-155 (1988), S. 1523-1524 
    ISSN: 0921-4534
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Physics
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Journal of Ultrasructure Research 81 (1982), S. 240-248 
    ISSN: 0022-5320
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Cell Biology International Reports 14 (1990), S. 44 
    ISSN: 0309-1651
    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
    Applied Surface Science 37 (1989), S. 337-352 
    ISSN: 0169-4332
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Physics
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Journal of comparative physiology 154 (1984), S. 81-87 
    ISSN: 1432-1351
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary The photoreceptive microvilli in the visual cells of the leech protrude into a large ‘intracellular vacuole’ which is but an extracellular compartment (ionic composition unknown), because it communicates with the extracellular space by narrow (≅ 20 nm) clefts (septate junctions) of unknown permeability properties. Application of Thiéry's cytochemical silver proteinate method reveals that the ‘vacuole’ contains carbohydrate-rich material. We used electron probe microanalysis of dry, ultrathin cryosections to determine quantitatively the elemental (K, Na, Cl, Mg, Ca, P, S) composition of the cytoplasm, ‘vacuole’ and extracellular space. The composition of the ‘vacuole’ is similar to that of the extracellular space, as shown by the comparable Na/K (11 to 13) and K/Ca (1.8 to 2.2) ratios in these two compartments. There are neglible concentration gradients for Na, K and Cl between ‘vacuole’ and extracellular space. The ‘vacuole’ has a high S content and a relatively large deficit of Cl compared to [Na]+[K]+2 [Ca]. Thus the data indicate that the ‘vacuole’ is in ionic communication with the extracellular space and contains sulfonated glycoprotein(s) that can partially exclude Cl; electroneutrality is maintained in part by these organic anions. The cytoplasmic K concentration (393±30 mmol/kg dry wt) is comparable to that in other nerve cells. The cytoplasmic Cl concentration (216±14 mmol/kg dry wt) is relatively high: significantly (P〈0.001) higher than the cytoplasmic Na (130±15 mmol/kg dry wt). The high cytoplasmic Cl content is in excess of that predicted by passive distribution, and suggests the operation of a Cl pump.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Springer
    Journal of comparative physiology 174 (1994), S. 421-431 
    ISSN: 1432-1351
    Keywords: Phototransduction ; Photoreceptor ; Cytoplasmic calcium ; Microfluorometry ; Bee
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Abstract We have measured Cai at rest and upon light stimulation in the photoreceptors of the honeybee drone microfluorometrically with the fluorescent Ca2+ indicator dyes fura-2, fluo-3 and Ca-green 5N. In darkness, Cai was ∼ 90 nM after 5 min of dark adaptation. A saturating light step caused Cai to rise in the bulk cytoplasm to ∼ 750 nM within 1 s. Our measurements with the low affinity dye Ca-green 5N showed that bright 1-s light flashes cause a rapid increase in Cai which was graded with stimulus intensity. Ca-green 5N fluorescence reached a peak in about 200 ms, and then decayed to a slightly lower sustained plateau. The fluorescence signal peaked, when the receptor potential was repolarizing from its peak to the plateau. This observation is in agreement with the proposal that the peak-to-plateau transition of the receptor potential is caused by the rise in Cai From our Fluo-3 measurements it appears that the latency of the Ca2+ increase is by 3–4 ms longer than the latency of the receptor potential elicited by bright 100-ms light flashes. This result provides no support for the proposal that Ca2+ mediates the opening of those membrane channels responsible for the upstroke of the receptor potential.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Springer
    Journal of comparative physiology 186 (2000), S. 497-503 
    ISSN: 1432-1351
    Keywords: Key words Honeybee ; Photoreceptors ; Spikes ; Ca2+ channels ; Neomycin
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Abstract Photoreceptor cells of the honeybee drone fire, in the presence of the polycationic aminoglycoside neomycin, repetitive slow spike-like potentials superimposed on the receptor potential plateau phase. We have used conventional intracellular recordings and microfluorometric intracellular Ca2+ measurements to characterize these spike potentials. We have shown that the spike frequency increases in a light-intensity-dependent manner. The spikes are fired only when light stimuli depolarize the cell from a resting potential of −50 to −60 mV to at least −40 to −45 mV; they are tetrodotoxin insensitive and blocked by the Ca2+ channel blockers Ni2+, Cd2+, ω-agatoxin TK, verapamil and methoxyverapamil. Depolarization of the photoreceptors with high extracellular K+ in the presence of neomycin in darkness does not generate spikes. Small intracellular Ca2+ oscillations superimposed on the plateau phase of the light-induced increase in intracellular free Ca2+ concentration have a similar temporal pattern as the spike-like potentials. We conclude that the spike-like potentials require stimulation by light and are generated by voltage-dependent Ca2+ channels localized on the soma of the photoreceptors, distal to the basal lamina.
    Type of Medium: Electronic Resource
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  • 9
    ISSN: 1615-6102
    Keywords: Ciliata ; Crystals ; Euplotes ; Lithosomes ; Microanalysis ; Ultrastructure
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary In the cytoplasm of the marine ciliateEuplotes vannus, there exist two conspicuous types of membrane bound inclusions: 1. irregularly shaped crystals which are highly anisotropic; 2. globular lithosomes characterized by concentrically arranged layers of deposits which exhibit only faint birefringence. Normally, both structures form distinct accumulations. Energy dispersive X-ray microanalysis of these accumulations reveals a high content of calcium and phosphorus, besides magnesium, sulphur and chlorine. Analysis of cell areas devoid of the inclusions show significantly lower calcium- and phosphorus-peaks.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Springer
    Histochemistry and cell biology 102 (1994), S. 271-277 
    ISSN: 1432-119X
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Abstract Carbonic anhydrase (CA) activity was localized in the salivery glands of the cockroach, Periplaneta americana, by (1) Hansson's histochemical technique, and (2) the use of the fluorescent sulphonamide, 5-dimethyl-amino-naphthalene-1-sulphonamide (DNSA). Both techniques reveal the same distribution pattern of CA in the four morphologically different cell types of the glands: peripheral cells, central cells, inner acinar duct cells, and distal duct cells. Positive reactions with Hansson's cobalt/phosphate technique were found in the apical regions of the peripheral cells and the distal duct cells, and were inhibited by 10−5 M acetazolamide in control experiments. No staining could be detected in the central cells and the inner acinar duct cells. The fluorescent CA inhibitor DNSA (10−4 M) specifically stained the peripheral cells and the distal duct cells in methanolfixed cryostat sections, whereas the central cells and the inner acinar duct cells remained unstained. The role of CA in the peripheral cells is not clear. CA activity in the distal duct cells may provide the protons needed to run the vacuolar-type H+-ATPase on the apical infoldings of the cells. This ATPase may be involved in modification of the primary saliva.
    Type of Medium: Electronic Resource
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