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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Germination (%)<br />
50<br />
40<br />
30<br />
20<br />
10<br />
0<br />
77<br />
Control (water)<br />
68<br />
Control (HS 50%)<br />
Treatment<br />
4.3.4. Ex vitro germination experiments<br />
62<br />
-N<br />
64<br />
-P<br />
87<br />
-K<br />
GA3 (10 -5 M)<br />
65<br />
Kinetin (10 -5 M)<br />
KNO 3 (10 -5 M)<br />
* *<br />
IBA (10 -5 M)<br />
NAA (10 -5 M)<br />
IAA (10 -5 M)<br />
Smoke water (1:500)<br />
Germination physiology<br />
Butenolide (10 -8 M)<br />
Figure 4.5: Effect <strong>of</strong> nutrients without N, P or K, plant growth promoting substances and<br />
smoke constituents on seed germination <strong>of</strong> Romulea rosea under 16 h photoperiod at 20<br />
± 0.5°C. A number above the standard error bar represents mean germination time and an<br />
asterisk denotes that the treatment was significantly different from the control (water)<br />
according to LSD test at the 5% level.<br />
Germination was observed for the four tested Romulea species. R. diversiformis<br />
seeds showed the highest percentage germination when placed at 10°C under<br />
alternating light (16 h photoperiod), in the constant dark conditions and with seed<br />
scarification treatment (Table 4.2). These results were significantly different from<br />
other treatments for R. diversiformis, with the exception <strong>of</strong> constant dark at 15°C,<br />
where it did not differ significantly in some cases. Although acid scarification<br />
66<br />
67<br />
68<br />
68<br />
68<br />
108