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Liquid Culture Systems for in vitro Plant Propagation

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498 Han Bouman & Annemiek Tiekstra<br />

3.2 Cymbidium<br />

The elemental analysis of adult leaves of Cymbidium is shown <strong>in</strong> table 1<br />

and orig<strong>in</strong>ates from Bergmann (1992). From these values, the composition<br />

of Cymbidium adapted medium (CAM) was calculated (Table 1). As orchids<br />

are normally grown on low-salt concentration media (<strong>in</strong> this case ½ MS,<br />

personal communication P+S <strong>Plant</strong>lab), a N-content of 30 mmol was<br />

adopted and on the basis of this concentration, the other elemental<br />

concentrations were calculated. In CAM, P, Ca and Mg contents are much<br />

higher <strong>in</strong> comparison with ½ MS. Almost no precipitation occurred, even<br />

after autoclav<strong>in</strong>g, probably because of the relatively low concentrations of<br />

Ca and P and the relatively high concentration of sulphate. Dur<strong>in</strong>g other<br />

adaptations, it was often observed that, while other concentrations were kept<br />

the same, <strong>in</strong>creas<strong>in</strong>g salt concentration with potassium sulphate dim<strong>in</strong>ished<br />

the precipitation of salts after autoclav<strong>in</strong>g, possibly because sulphate has<br />

some buffer<strong>in</strong>g and complex-<strong>for</strong>m<strong>in</strong>g capacity.<br />

For all three cultivars, growth <strong>in</strong>creased significantly by culture with<br />

CAM compared to ½ MS and ½DKW (Table 2). For shoot <strong>for</strong>mation,<br />

root<strong>in</strong>g and acclimatisation there were no differences <strong>in</strong> m<strong>in</strong>eral media and<br />

the per<strong>for</strong>mance of the propagules was the same irrespective of the orig<strong>in</strong>al<br />

propagation medium. It is possible that further improvements could be<br />

achieved by m<strong>in</strong>eral adaptations <strong>in</strong> these steps. The nutrient concentration<br />

ratios used <strong>in</strong> ½MS compared with those applied <strong>in</strong> hydroponics (Table 1)<br />

are 1.5 <strong>for</strong> Ca, 1.0 <strong>for</strong> Mg and 0.76 <strong>for</strong> P. In ½DKW these ratios are 4.7, 2.0<br />

and 1.2, respectively and <strong>in</strong> CAM 6.7, 3.7 and 2.0, respectively. This<br />

<strong>in</strong>dicates that the concentrations of Ca, Mg and P are too low <strong>in</strong> MS and -to<br />

a lesser extent- <strong>in</strong> DKW. The CAM medium supplies these three elements at<br />

a more appropriate concentration. For K and N <strong>in</strong> all 3 media, these ratios<br />

are similar viz., ca. 3.5 and 5.5, respectively.<br />

After the 3-week cycle, the media were analysed <strong>for</strong> elemental content<br />

(data not shown). None of the major m<strong>in</strong>erals was exhausted with the<br />

notable exception of P (8 % of the orig<strong>in</strong>al concentration rema<strong>in</strong>ed <strong>in</strong> the<br />

medium). Phosphorous, particularly, is known to be consumed <strong>in</strong> a ‘luxury’<br />

way, i.e., the plant takes up more than needed <strong>for</strong> immediate growth<br />

(George, 1993). Concern<strong>in</strong>g nitrogen, it was found that the f<strong>in</strong>al amount of<br />

ammonium was rather low (ca 10 % rema<strong>in</strong>ed), but that ca 50 % of the<br />

nitrate was still present. Especially <strong>in</strong> the CAM medium with the faster<br />

grow<strong>in</strong>g plant material, sucrose concentration became low, but was not<br />

exhausted (approximately 10 % rema<strong>in</strong>ed).

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