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

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

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temperatures. Some show serious internal discoloration after prolonged storage at<br />

several degrees above their actual freezing point, while others may not show injury<br />

at –1.7 °C, the average freezing point <strong>of</strong> most potato varieties.<br />

Freezing injury <strong>of</strong> celery can be readily recognized at harvest time by the flabby<br />

water-soaked condition <strong>of</strong> the leaves <strong>and</strong> leaf stalks. Frozen leaves, if not attacked<br />

by bacteria, dry out <strong>and</strong> become papery. A second type <strong>of</strong> freezing symptom is<br />

the appearance <strong>of</strong> isolated sunken lesions on the leafstalks. These two types <strong>of</strong> injury<br />

are most <strong>of</strong>ten apparent at harvest but are <strong>of</strong> little importance on the market.<br />

3.3. Mineral nutrient disorders<br />

In this section the key nutrients causing physiological disorders <strong>and</strong> their role in<br />

vegetables will be discussed. A mineral nutrient can function as a constituent <strong>of</strong><br />

an organic structure, as an activator <strong>of</strong> enzyme reactions or as a charge carrier<br />

<strong>and</strong> osmo-regulator.<br />

3.3.1. Calcium<br />

Effect <strong>of</strong> Preharvest Factors 13<br />

Calcium is a relatively large, divalent cation. The Calcium content <strong>of</strong> plants varies<br />

between 0.1 <strong>and</strong> > 0.5% <strong>of</strong> dry weight depending on the growing conditions, plant<br />

species, <strong>and</strong> plant organ. Genotypically differences in Ca 2+ requirements are closely<br />

related to the Ca 2+ binding sites in the cell walls. Ca deficiency in plant tissues causes<br />

many physiological disorders which lead to significant losses in plant production.<br />

Calcium shortage in plants is related to poor Ca uptake, its limited movement<br />

to above – ground plant parts <strong>and</strong> strong competition for Ca between leaves <strong>and</strong><br />

generative plant parts (fruits, seeds) (Wojcik, 1998).<br />

Calcium readily enters the apoplasm <strong>and</strong> is bound in an exchangeable form to<br />

cell walls <strong>and</strong> at the exterior surface <strong>of</strong> the plasma membrane. Its rate <strong>of</strong> uptake<br />

into the cytoplasm is severely restricted <strong>and</strong> seems to be only loosely coupled to<br />

metabolic processes. The mobility <strong>of</strong> Ca from cell to cell <strong>and</strong> in the phloem is<br />

very low. It is the only mineral nutrient other than Bo which functions mainly outside<br />

the cytoplasm in the apoplasm. Most <strong>of</strong> its activity is related to its capacity for<br />

co-ordination by which it provides stable but reversible intermolecular linkages;<br />

predominantly in the cell walls <strong>and</strong> the plasma membrane. These Ca 2+ mediated<br />

linkages respond to local changes in environmental conditions <strong>and</strong> are part <strong>of</strong> the<br />

control mechanism <strong>of</strong> growth <strong>and</strong> developmental processes. Calcium is a nontoxic<br />

mineral nutrient, even in high concentrations, <strong>and</strong> is very effective in<br />

detoxifying high concentrations <strong>of</strong> other mineral elements in plants.<br />

There are two distinct areas in the cell wall with high Ca 2+ concentrations, the<br />

middle lamella <strong>and</strong> the extension surface <strong>of</strong> the plasma membrane. In both areas<br />

Ca 2+ has essential structural functions, namely, the regulation <strong>of</strong> the membrane<br />

permeability <strong>and</strong> related processes <strong>and</strong> the strengthening <strong>of</strong> the cell walls.<br />

The fundamental role <strong>of</strong> Ca 2+ in membrane stability <strong>and</strong> cell integrity is reflected<br />

in various ways. It can be demonstrated most readily by the increased leakage <strong>of</strong><br />

low molecular weight solutes (e.g. in tomato fruits; Goor, 1968) <strong>and</strong> in severely<br />

deficient plants, by a general disintegration <strong>of</strong> membrane structures (Hecht-Buchholz,

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