View/Open - ResearchSpace - University of KwaZulu-Natal
View/Open - ResearchSpace - University of KwaZulu-Natal
View/Open - ResearchSpace - University of KwaZulu-Natal
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In vitro culture initiation and multiplication<br />
Figure 5.7: Visual observations <strong>of</strong> Romulea sabulosa cultures. Cultures including both kinetin<br />
and 2,4-D appears to exhibit embryo-like structures.<br />
5.3.3 Explant comparison<br />
Despite the apparent larger number <strong>of</strong> shoots produced between cultures in which<br />
embryos were used as explants compared to seedling organs, there is no significant<br />
difference between the numbers <strong>of</strong> shoots produced according to a paired t-test at<br />
95% confidence limits. There was also no significant difference between the number<br />
<strong>of</strong> shoots formed on media supplemented with kinetin and the number <strong>of</strong> shoots<br />
formed on media supplemented with other plant growth regulator treatments (Figure<br />
5.8). These results show that a medium supplemented with 23.2 µM mTR and 0.5 µM<br />
NAA significantly increases the amount <strong>of</strong> shoots formed per embryo compared to<br />
the control. This is not the case with seedling hypocotyls. Here cytokinins did not<br />
increase the number <strong>of</strong> shoots formed per explant (Figure 5.8). The number <strong>of</strong><br />
shoots produced on a medium with 23.2 µM mTR and 0.5 µM NAA was not<br />
significantly different from the number <strong>of</strong> shoots observed on a medium<br />
supplemented with 2.3 µM kinetin or 2.3 µM mTR and 0.5 µM NAA.<br />
Explant response data is not shown, as there were no significant differences in<br />
explant response between the two explant types. Although these differences are not<br />
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