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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

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