Titlebook: Biophysical control of microfibril orientation in plant cell walls; Aquatic and terrestr J. D. Boyd Book 1985 Springer Science+Business Med

TOM

https://doi.org/10.1057/9781137003423he influence of turgor pressure has ceased. For wood fibres,* there are many more data on the wide range of variations in the architecture of secondary walls, than is the case with other cells and plants; hence this discussion will be concentrated on wood fibres. However, in respect of the generally

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Chromatic

https://doi.org/10.1057/9781137003423d substantially. There has been a big increase also in knowledge of the physical form and some biochemical aspects of organelles within the protoplasm of the cell. Regretably however, the literature has not provided commensurate enlightenment on how the development of the plant cell wall is controll

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STRIA

https://doi.org/10.1057/9781137319241fibril arrangements in tip growth of cells, which led to Roelofsen and Houwink’s (1953) formulation of MGH, to explain variations in microfibril orientation at different positions in the thickness of the cell wall.

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stratum-corneum

Reassessment of data on tip growth and conclusions on MGH,fibril arrangements in tip growth of cells, which led to Roelofsen and Houwink’s (1953) formulation of MGH, to explain variations in microfibril orientation at different positions in the thickness of the cell wall.

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Introduction,ortant physical features, which are similar for a wide variety of types of plant cell walls include: (i) basic structural elements of crystalline polysaccharides, which are aggregated in the form of microfibrils, and thus provide high strength and stiffness in their longitudinal direction; (ii) the