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Production Practices and Quality Assessment of Food Crops. Vol. 1

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which depends on climate <strong>and</strong> irrigation, was assumed to be inversely proportional<br />

to the maximum daily shrinkage (MDS) <strong>of</strong> trunks measured using the<br />

micromorphometric method (Huguet, 1985; Garnier <strong>and</strong> Berger, 1986).<br />

The model assumes that trees are optimally fertilized <strong>and</strong> that carbon acquisition<br />

by photosynthesis is sufficient for well-irrigated trees to reach full potential fruit<br />

growth. The fruit receives a daily solution flow from the plant (F) <strong>and</strong> loses water<br />

by transpiration (T) <strong>and</strong> carbon by respiration (R). Thus growth is<br />

dW fresh = F – R – T<br />

dt<br />

Modelling Fruit <strong>Quality</strong> 65<br />

Respiration is calculated as in the SWAF model. Transpiration is a function <strong>of</strong><br />

fruit mass (W fresh), hourly global solar radiation (GR) <strong>and</strong> skin area <strong>of</strong> the fruit<br />

(Génard <strong>and</strong> Huguet, 1996).<br />

The model assumes that a maximal flow (F max) is determined by the restricted<br />

vascular cross-sectional area <strong>of</strong> the fruit peduncle. Moreover, the solution flow is<br />

considered to increase <strong>and</strong> decrease with plant <strong>and</strong> fruit water potential, respectively,<br />

which has been stated for xylem flow <strong>and</strong> is thought to be effective for phloem<br />

flow towards the fruit (Lang et al., 1986), though the process involved is more<br />

complex. The water potential <strong>of</strong> a fruit depends on the osmotic potential <strong>of</strong> its<br />

cells, which is usually related to sugar content in the fruit, <strong>and</strong> on the pressure<br />

potential due to the resistance <strong>of</strong> tissues to deformation. Sugar concentration<br />

increases with fruit transpiration per unit mass <strong>and</strong> with peach mass as indicated<br />

by Chapman et al. (1991) <strong>and</strong> Génard et al. (1991). Pressure potential seems to<br />

increase with fruit size (Bussières, 1994). The plant water potential is assumed to<br />

be inversely proportional to MDS.<br />

Consequently, the model assumes that the flow:<br />

– has a maximal value F max;<br />

– increases with fruit mass (W fresh) <strong>and</strong> with transpiration per unit mass (T w), since<br />

W fresh <strong>and</strong> T w will cause a decrease in the osmotic potential <strong>of</strong> the fruit;<br />

– levels <strong>of</strong>f at high fruit size, when the fruit pressure potential compensates for<br />

the decrease in osmotic potential;<br />

– decreases with MDS.<br />

According to the previous assumptions, the flow is computed using the following<br />

empirical equation<br />

F = A 1(1 – e –A2(WfreshTw)A3) with A i = a i<br />

<strong>and</strong> otherwise F = F max<br />

MDS ( )<br />

MDSo<br />

where A i are empirical functions <strong>of</strong> the effect <strong>of</strong> water stress on the daily solution<br />

flow F, <strong>and</strong> a i, b i <strong>and</strong> F max parameters. MDSo is a calibration parameter related to<br />

the trunk characteristics <strong>of</strong> the tree. The product W fresh T w is equal to fruit transpiration<br />

(T), which is an important stimulator <strong>of</strong> fruit growth in the model.<br />

bi<br />

, if F < F max

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