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Titlebook: Stomata; Colin Willmer,Mark Fricker Book 1996Latest edition Springer Science+Business Media Dordrecht 1996 Plant physiology.biology.cell.d

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sistance battery models used in vehicle simulations or energy storage system simulations (Zhang et al. in Energy conversion congress and exposition, pp. 3270–3277, .; Chen et al. in International conference on electric information and control engineering, pp. 2601–2604, .) even involving fast dynami
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Ionic relations of stomatal movement and signal transduction in guard cells,gh sufficient data is beginning to accumulate to establish interactions in the signalling net- work that are unique to guard cells. In this chapter the mechanisms leading to reversible ion accumulation and release by guard cells are considered, followed by a discussion of how such ion fluxes are regu- lated by internal and external signals.
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Stomatal responses to environmental factors, possess functional plasmodesmata (see Chapter 3). Thus, because of their relative isolation from the rest of the plant body, stomata are ideally suited for sensing and responding to environmental factors.
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The mechanics of stomatal movements,ard cells and epidermal tissue, and the different modes of deformation of guard cells during stomatal movements. Additionally, the osmotic relations of guard cell protoplasts (GCPs) will be considered, including the dynamics of membrane recycling.
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The theory of gas diffusion through stomata,of gases through stomata. The vari- ous techniques for measuring stomatal resistance, or its reciprocal, stomatal conductance, have been extensively covered elsewhere (see, e.g. Sestak .., 1971; Weyers and Meidner, 1990).
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The distribution of stomata,ds suggest that stomata were relatively large in early plants. In ., stomata up to 120 µm long were recorded (Lele and Walton, 1960–61). These are the largest stomata that have been measured in living or extinct plants.
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