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  • Articles: DFG German National Licenses  (2)
  • 1975-1979  (2)
  • Brownian motion  (1)
  • Crystalline fibril  (1)
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  • Articles: DFG German National Licenses  (2)
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  • 1975-1979  (2)
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  • 1
    ISSN: 1432-2048
    Keywords: Crystalline fibril ; Endoplasmic reticulum ; Nymphoides ; Protophloem
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Endoplasmic reticulum in the root protophloem of Nymphoides peltata (S.G. Gmel.) O. Kuntze changes form as sieve elements differentiate. In immature sieve elements the individual endoplasmic reticulum (ER) cisternae form large irregular aggregates in the cytoplasm. In older immature sieve elements the ER aggregates are more ordered and membranes in them are convoluted. Although convoluted ER predominates in immature sieve elements the ER of the mature sieve elements consists mainly of flattened stacks of ER cisternae. Some of these stacks of ER may be derived from the existing convoluted ER. “Crystalline fibrils” first appear in the cytoplasm of the sieve element when the ER starts to aggregate. The crystalline fibrils move to the parietal layer of the sieve element along with the aggregates of ER. A possible ontogenetic relationship between ER and crystalline fibrils is discussed.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Planta 143 (1978), S. 191-205 
    ISSN: 1432-2048
    Keywords: Brownian motion ; Freeze-etching ; Nymphoides ; Phloem ; P. protein ; Sieve pores ; Translocation (phloem)
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Intact vascular bundles from Nymphoides peltata (S.G. Gmel.) O. Kuntze, shown to have translocated carbon-14, were freeze-fractured and etched for electron microscopy. The interpretation of freezefractured and etched sieve pores and P-protein filaments seen in them is discussed. The entire widths of most of the sieve pores seen contained filaments separated by less than 100 nm. Their arrangement indicates too high a resistance to flow for pressure flow alone to drive translocation at known rates; pumps would be necessary at places along sieve tubes. However, calculations are presented to show that during the time taken to fix pores, by fast freezing or chemically, the filaments in them could rearrange and move further by Brownian and other motion than the distances between filaments which we need to measure. These calculations show that it is not possible, by microscopy alone, to answer the outstanding question “How are filaments arranged in translocating sieve pores?” with enough certainty to tell us whether pressure flow is adequate to explain translocation where filaments are present. The calculations are relevant also to microscopy of other cell structures which may move.
    Type of Medium: Electronic Resource
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