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Liquid Culture Systems for in vitro Plant Propagation

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408 V.A. Savangikar et al.<br />

In mak<strong>in</strong>g cost calculations <strong>for</strong> the new and old model, follow<strong>in</strong>g factors<br />

are considered:<br />

a) Repayment on capital assets considered at 20% each year. Capital cost <strong>in</strong><br />

new model be<strong>in</strong>g 25% of the capital cost <strong>for</strong> old model. It is presumed<br />

that capital costs shall be similar <strong>in</strong> all countries.<br />

b) Interest (per annum) on capital cost considered at 18% <strong>for</strong> develop<strong>in</strong>g<br />

countries and at 4% <strong>for</strong> developed countries.<br />

c) Depreciation on capital assets considered at 10% per annum.<br />

d) Electrical consumption <strong>in</strong> new model, 33% of the old model.<br />

e) Labour cost <strong>in</strong> develop<strong>in</strong>g countries is considered to be US $ 0.73 per<br />

day (8 hour shift). Same <strong>in</strong> developed countries is taken to be US $ 40<br />

per day (8 hour shift).<br />

f) Costs <strong>in</strong> primary and secondary harden<strong>in</strong>g are not <strong>in</strong>cluded <strong>in</strong> cost<br />

calculations as the location-specific differences, purpose specific<br />

requirements/imperatives and species specific imperatives differ widely<br />

and should be separately considered. Further, they are not a part of the<br />

micropropagation model and should be assessed entirely separately.<br />

3. Results and discussion<br />

Production from the new model was more reliable than the old model <strong>in</strong><br />

terms of general vigor, contam<strong>in</strong>ation control and productivity.<br />

Multiplication and root<strong>in</strong>g were also achieved simultaneously. The<br />

multiplication culture l<strong>in</strong>es <strong>in</strong>itiated with use of old model medium <strong>in</strong> liquid<br />

<strong>for</strong>m (by omitt<strong>in</strong>g agar) lost vigor slowly with every subculture and despite<br />

the application of visual <strong>in</strong>dex<strong>in</strong>g, were subject to high rates of<br />

contam<strong>in</strong>ation and were discont<strong>in</strong>ued eventually. The new model cultures<br />

<strong>in</strong>itiated with the new liquid medium and visual <strong>in</strong>dex<strong>in</strong>g were also subject<br />

to fluctuat<strong>in</strong>g contam<strong>in</strong>ation <strong>in</strong>cidents, but cont<strong>in</strong>ued to be vigorous and<br />

ultimately settled to a steady production rate. These stabilized l<strong>in</strong>es are the<br />

<strong>in</strong>puts <strong>for</strong> the work which has given the reported and analysed data. It was<br />

also seen that success <strong>in</strong> primary harden<strong>in</strong>g <strong>in</strong> plants derived from the new<br />

model was better than the plants derived from the old model. This was<br />

ma<strong>in</strong>ly due to the acclimatization effect, which the plants get already <strong>in</strong><br />

culture developmental stage <strong>in</strong> the new model i.e. development of hard<strong>in</strong>ess<br />

<strong>in</strong> leaves, stem and profuse root<strong>in</strong>g <strong>in</strong> culture itself as response to high<br />

<strong>in</strong>tensity of natural illum<strong>in</strong>ation of the cultures while they are undergo<strong>in</strong>g<br />

differentiation and multiplication while hang<strong>in</strong>g <strong>in</strong> the greenhouse. Ziv<br />

(1986) has also ma<strong>in</strong>ta<strong>in</strong>ed that acclimatization <strong>in</strong> <strong>vitro</strong> is the best possible

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