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

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22 1 Chemistry <strong>and</strong> Structure <strong>of</strong> <strong>Cuticles</strong> as Related to <strong>Water</strong> <strong>and</strong> <strong>Solute</strong> <strong>Permeability</strong><br />

Area <strong>of</strong> epidermal cells (µm 2 )<br />

8000<br />

7000<br />

6000<br />

5000<br />

4000<br />

3000<br />

2000<br />

1000<br />

Thickness (µm)<br />

12<br />

10<br />

8<br />

6<br />

4<br />

cell wall<br />

cuticular layer<br />

2<br />

0<br />

cuticle proper<br />

0 5 10 15 20<br />

Distance from leaf base (cm)<br />

0<br />

0 5 10 15 20<br />

Distance from leaf base (cm)<br />

Fig. 1.7 Development <strong>of</strong> epidermal cells <strong>and</strong> adaxial epidermis <strong>of</strong> Clivia miniata leaves. (Redrawn<br />

from Riederer <strong>and</strong> Schönherr 1988)<br />

The adaxial cuticle <strong>of</strong> Clivia miniata leaves has a laminated CP, <strong>and</strong> is ideally<br />

suited to study cuticle development. Clivia is a monocot, <strong>and</strong> leaves grow at their<br />

base such that cuticle age increases in direction to the leaf tip. Size <strong>of</strong> epidermal<br />

cells, thickness <strong>of</strong> cuticles <strong>and</strong> cell wall, cutin composition, cutin biosynthesis <strong>and</strong><br />

fine structure have been investigated as a function <strong>of</strong> position, that is <strong>of</strong> age (Mérida<br />

et al. 1981; Schmidt <strong>and</strong> Schönherr 1982; Lendzian <strong>and</strong> Schönherr 1983; Riederer<br />

<strong>and</strong> Schönherr 1988).<br />

Between position 1 cm <strong>and</strong> 5 cm, the projected area <strong>of</strong> epidermal cells increased<br />

about ninefold from 800µm 2 to 7,000µm 2 . Afterwards, cell area no longer changed.<br />

At the same positions, cell length increased from 50 to 250µm (Riederer <strong>and</strong> Schönherr<br />

1988); that is, epidermis cells increased both in length <strong>and</strong> width up to position<br />

5 cm (Fig. 1.7).<br />

The CP was synthesised first <strong>and</strong> its thickness increased up to 3 cm from leaf<br />

base. Fine structure also changed. Maximum thickness <strong>of</strong> CP was about 200–<br />

250 nm, <strong>and</strong> it increased no further between 3 <strong>and</strong> 20 cm (Figs. 1.7 <strong>and</strong> 1.8 inset).<br />

Starting at position 3 cm the cuticular layer developed, <strong>and</strong> it increased in thickness<br />

up to position 20 cm from leaf base. Fine structure <strong>of</strong> the CL (Fig. 1.8) <strong>and</strong><br />

chemistry (Riederer <strong>and</strong> Schönherr 1988) changed significantly.<br />

Lamellation <strong>of</strong> the CP is best seen at 3 cm from base. At higher positions (>4cm)<br />

the central part <strong>of</strong> the CM has little contrast, probably because OsO4 does not penetrate<br />

because the CP is incrusted with waxes. The cuticular layer starts to develop at<br />

position 3 cm <strong>and</strong> increases in thickness at higher (older) positions. The CL is initially<br />

reticulate, but in old <strong>and</strong> mature positions fine structure has disappeared. It is<br />

25

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