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Liquid Culture Systems for in vitro Plant Propagation

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270 Kater<strong>in</strong>a Grigoriadou et al.<br />

of cont<strong>in</strong>uous culture <strong>in</strong> the TIS <strong>for</strong> 30 days (Table 2, Figure 6).<br />

Hyperhydricity was apparent but not as serious as <strong>in</strong> the other liquid system<br />

devices tested. In the case where cultures <strong>in</strong> TIS were comb<strong>in</strong>ed with agar<br />

solidified medium (10 and 20 days, respectively) the number of new<br />

microshoots per explant was 0.64 with a significant <strong>in</strong>creased shoot length of<br />

1.40 cm (Table 2). When explants were ma<strong>in</strong>ta<strong>in</strong>ed <strong>for</strong> 20 days <strong>in</strong> TIS<br />

followed by 10 days <strong>in</strong> agar solidified medium, the respective results were<br />

1.41 and 0.70 cm (Table 2). In both treatments hyperhydricity problems<br />

were not observed.<br />

<strong>Culture</strong>s <strong>in</strong> agar-solidified medium, which were used as control, resulted<br />

<strong>in</strong> 1.75 new microshoots per explant of 1.22 cm average shoot length<br />

(Table 2).<br />

a b<br />

c<br />

c d<br />

Figure 4: <strong>Culture</strong> of olive microshoots <strong>in</strong> Erlenmeyer flasks under agitation (a and b) and on<br />

filter paper bridges <strong>in</strong> test tubes (c and d). In d, arrows po<strong>in</strong>t to callus masses.

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