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4.14<br />

importance <strong>of</strong> the time between anthesis and mahirity by intmducing genes for early<br />

flowefing in<strong>to</strong> a B. napus line and a 8. rapa population. Thurling (1991) concluded that<br />

the earlier flowefing resulted in a longer period <strong>of</strong> dry matter accumulation and greater<br />

seed yields. <strong>The</strong> later Rowering did not adversely affêct the performance <strong>of</strong> the<br />

composite populations in this study with the exception <strong>of</strong> the Reward Ct4 which was<br />

later flowering in Cannan. <strong>The</strong>re was a positive correlation between days <strong>to</strong> Rowering<br />

and seed yield for the Reward C, population in Carman (Table 4.8). A negative<br />

correlation between days <strong>to</strong> flowering and seed yield was found with the Reward and<br />

DSC-3 DH lines and DSC-3 C, and C, populations in Cannan (Table 4.8).<br />

CONCLUSION<br />

<strong>The</strong> production <strong>of</strong> composite populations from DH lines has the potential <strong>of</strong><br />

speeding up cultivar devalopment. As a breeding <strong>to</strong>ol, irnprovements can be made in<br />

B. rapa populations by selecting OH lines with fixed traits followed by randorn<br />

interpollination <strong>to</strong> recover per<strong>to</strong>mance. This method avoids the short comings <strong>of</strong><br />

traditional breeding systems such as the time required for repeated generations <strong>of</strong><br />

inbreeding and selection seen with mass selection, the difficulty in producing a reliable<br />

pollination control system for hybrid production and the maintenance <strong>of</strong> original entries<br />

for reconstitution <strong>of</strong> a population as a synthetic.<br />

<strong>The</strong> individual DH lines do not exceed donor population performance but, when<br />

crossed <strong>to</strong> establish a composite, population performance can be recovered. This

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