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Water and Solute Permeability of Plant Cuticles: Measurement and ...

Water and Solute Permeability of Plant Cuticles: Measurement and ...

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4.6 <strong>Water</strong> <strong>Permeability</strong> <strong>of</strong> Isolated Astomatous Cuticular Membranes 115<br />

Fig. 4.22 Transport chamber used for measuring the flux <strong>of</strong> 3 H-labelled water from the donor<br />

across stomatous cuticles into the receiver. In the receiver was a water-saturated filter paper<br />

(depicted in dark blue) absorbing 3 H-labelled water which diffused across the CM. The revolving<br />

rod allows sampling <strong>of</strong> the receiver without changing the atmosphere in the receiver. (Modified<br />

from Santrucek et al. 2004)<br />

The fact that resistance <strong>of</strong> fatty alcohols is a function <strong>of</strong> log nC could explain why<br />

evolution selected very long chain wax monomers for building a water barrier. At<br />

ambient temperatures these monomers are in the solid state, <strong>and</strong> very small amounts<br />

<strong>of</strong> 1–2 µgcm −2 suffice. We are again confronted with the question why wax coverage<br />

is much higher with most plants (Tables 1.1, 4.6, 4.7 <strong>and</strong> 4.11). Leaves can be<br />

subjected to considerable abiotic (e.g., wind, rain, ice <strong>and</strong> storm) <strong>and</strong> biotic forces<br />

(e.g., insects, fungi <strong>and</strong> bacteria). This should lead to a continuous disturbance <strong>of</strong><br />

a highly ordered wax structures on the leaf surface, <strong>and</strong> losses <strong>of</strong> wax might even<br />

occur during the season. A fast <strong>and</strong> efficient compensation <strong>of</strong> this disturbance, keeping<br />

the cuticular transport barrier intact, might require fairly high amounts <strong>of</strong> wax

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