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

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168 6 Diffusion <strong>of</strong> Non-Electrolytes<br />

Table 6.6 Amounts <strong>of</strong> surface wax, projected <strong>and</strong> specific surface areas <strong>and</strong> permeances <strong>of</strong> conifer<br />

needles from Abies koreana, Abies alba, Picea pungens <strong>and</strong> Pinus sylvestris (Schreiber <strong>and</strong><br />

Schönherr 1992b)<br />

Species Surf. wax Aprojected Aspecific <strong>Solute</strong> Pspecific Pprojected<br />

(µg mm −1 ) (mm 2 mm −1 ) (mm 2 mm −1 ) (m s −1 ) (m s −1 )<br />

A. koreana 7.10 5 683 2,4-D 2.71 × 10 −11 3.70 × 10 −9<br />

A. alba 2.50 5 254 2,4-D 3.11 × 10 −11 1.58 × 10 −9<br />

P. pungens – 3 65.7 2,4-D 2.24 × 10 −11 4.91 × 10 −10<br />

P. sylvestris – 3 41.3 2,4-D 3.78 × 10 −11 5.22 × 10 −10<br />

P. abies 1.56 3 29.4 2,4-D 3.51 × 10 −11 3.43 × 10 −10<br />

A. koreana 7.10 5 683 Triadim 2.54 × 10 −11 3.47 × 10 −9<br />

A. alba 2.50 5 254 Triadim 5.58 × 10 −11 2.83 × 10 −9<br />

P. pungens – 3 65.7 Triadim 7.00 × 10 −11 1.53 × 10 −9<br />

P. abies 1.56 3 29.4 Triadim 4.00 × 10 −11 3.92 × 10 −9<br />

P. pungens – 3 65.7 Lindane 4.23 × 10 −10 9.26 × 10 −9<br />

P. sylvestris – 3 41.3 Lindane 5.01 × 10 −10 6.91 × 10 −9<br />

A. koreana 7.10 5 683 Bitertanol 4.23 × 10 −10 5.78 × 10 −8<br />

A. alba 2.50 5 254 Bitertanol 6.84 × 10 −10 3.47 × 10 −8<br />

P. pungens – 3 65.7 Bitertanol 7.95 × 10 −10 1.74 × 10 −8<br />

P. abies 1.56 3 29.4 Bitertanol 4.36 × 10 −10 4.27 × 10 −9<br />

A. koreana 7.10 5 683 PCP 4.20 × 10 −9 5.74 × 10 −7<br />

A. alba 2.50 5 254 PCP 3.90 × 10 −9 1.98 × 10 −7<br />

P. pungens – 3 65.7 PCP 6.63 × 10 −9 1.45 × 10 −7<br />

P. sylvestris – 3 41.3 PCP 3.30 × 10 −9 4.55 × 10 −8<br />

P. abies 1.56 3 29.4 PCP 5.00 × 10 −9 4.90 × 10 −8<br />

why both amounts penetrated <strong>and</strong> y-intercepts were highest (Fig. 6.8). The other<br />

chemicals had smaller partition coefficients than PCP, <strong>and</strong> for this reason sorption<br />

is smaller, <strong>and</strong> rates <strong>of</strong> penetration as well (Fig. 6.8).<br />

This correlation between rates <strong>of</strong> penetration <strong>and</strong> sorption in surface wax <strong>and</strong><br />

cuticles is not really surprising, since amounts sorbed <strong>and</strong> rates <strong>of</strong> penetration are<br />

proportional to concentration in the donor (6.6). After loading compartments 1 <strong>and</strong><br />

2 from the aqueous solution, the concentration in waxes <strong>and</strong> cuticles is the driving<br />

force for loading the mesophyll, at least as long as concentration <strong>of</strong> non-ionised<br />

PCP in the mesophyll remains small <strong>and</strong> insignificant <strong>and</strong> external concentration<br />

does not change.<br />

6.2.2.4 Projected <strong>and</strong> Specific Surface Area<br />

Whenever permeances are calculated, rates <strong>of</strong> penetration are divided by area <strong>and</strong><br />

donor concentration (6.6). Glaucous leaves have large amounts <strong>of</strong> epicuticular wax,<br />

which can greatly increase surface area. With regard to foliar penetration, the question<br />

arises as to how much <strong>of</strong> this surface wax area is in contact with the aqueous<br />

donor solution. This in turn depends on wetting, <strong>and</strong> in absence <strong>of</strong> surfactants it<br />

seems plausible that only the tips <strong>of</strong> the wax rodlets typical for barley <strong>and</strong> conifers

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