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Liquid Culture Systems for in vitro Plant Propagation

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488 Hans R. Gislerød et al.<br />

4.1 Light <strong>in</strong>tensity<br />

Light <strong>in</strong>tensity is the major factor affect<strong>in</strong>g photosynthesis and<br />

greenhouse temperatures dur<strong>in</strong>g the day. In addition the total hours of<br />

artificial light<strong>in</strong>g per cycle is important. The uptake of water and nutrients<br />

generally <strong>in</strong>crease as the light <strong>in</strong>tensity and air temperature <strong>in</strong>crease, while<br />

the air humidity decreases. Adams (1994) showed that the uptake of K and N<br />

<strong>for</strong> a tomato crop followed the water uptake, which was closely, related to<br />

the solar radiation, but was about an hour delayed. Increas<strong>in</strong>g light <strong>in</strong>tensity<br />

causes <strong>in</strong>creased growth, and that will demand an <strong>in</strong>creased rate of nutrient<br />

supply. This may be particularly important with use of artificial light <strong>in</strong><br />

w<strong>in</strong>ter, when the air humidity usually is high.<br />

In micropropagation carbohydrate is used as an energy source, because of<br />

low rates of photosynthesis. In the phase of <strong>in</strong> <strong>vitro</strong> to <strong>in</strong> vivo the<br />

acclimatisation is easier when the carbohydrate content of the medium has<br />

been reduced the last weeks be<strong>for</strong>e transplant<strong>in</strong>g (Selliah, unpublished<br />

results).<br />

Giv<strong>in</strong>g more light than optimal can, <strong>in</strong> some situations, cause iron<br />

deficiency. This is shown <strong>for</strong> both greenhouse crops and <strong>in</strong><br />

micropropagation <strong>in</strong> figure 1, and may happen when us<strong>in</strong>g EDTA as a<br />

chelate <strong>for</strong> iron (Papathanasiou et al., 1996). Organic chelates such as<br />

EDTA, are sensitive to light, and Fe deficiency may occur <strong>in</strong> some species<br />

under high light conditions. To elim<strong>in</strong>ate this problem, NaFe-EDTA can be<br />

replaced by Fe-EDDHA; alternatively, the light <strong>in</strong>tensity can be reduced.<br />

Fe-EDDHA is a more light-stable chelated Fe source than Fe-EDTA. It is<br />

now possible to purchase the pre-mixed tissue culture media with Fe-<br />

EDDHA.<br />

4.2 Humidity<br />

Recent measures to conserve energy <strong>in</strong> greenhouses have resulted <strong>in</strong><br />

higher humidity regimes, which reduce transpiration, and hence Ca<br />

movement <strong>in</strong>to the leaves, as Ca moves only <strong>in</strong> the xylem <strong>in</strong> most<br />

greenhouse crops. Conversely, high humidity allows more Ca to move <strong>in</strong>to<br />

the plant organs that have a low rate of transpiration, such as tomato fruit.<br />

Humidity, there<strong>for</strong>e, is a key factor <strong>in</strong> controll<strong>in</strong>g the distribution of some<br />

nutrients with<strong>in</strong> the plant.<br />

Increas<strong>in</strong>g air humidity from 55-60 % RH to 90-95 % RH reduced the<br />

concentration of the nutrient element <strong>in</strong> the leaves of ornamental greenhouse<br />

plants (Gislerød et al., 1987). There<strong>for</strong>e the concentration of the nutrient<br />

solution should be <strong>in</strong>creased when the plants are grown at a high RH. Adams<br />

(1994) showed <strong>for</strong> tomato grown at high air humidity that the marg<strong>in</strong> of the

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