Modification of potato microtuber dormancy during induction and growthin vitro orex vitro

Prolonged or highly variable dormancy can be a significant impediment to the efficient use of potato (Solanum tuberosum L.) microtubers by the seed industry. In the present study, reductions in microtuber dormancy duration were obtained in cultivars commonly used by the processing industry (Kennebec, Russet Burbank and Shepody). This was achieved by modifying microtuber induction media and applying various dormancy-release treatments after harvest, with or without prior storage. An 8 h photoperiod, instead of continuous darkness during microtuber induction and development, increased microtuber yield while reducing dormancy duration. Dormancy duration was also shortened by increased sucrose concentration during microtuber induction under an 8 h photoperiod. As sucrose was increased from 4 to 16% under an 8 h photoperiod, mean dormancy duration decreased by 86 d for Shepody, 65 d for Kennebec and 46 d for Russet Burbank. During theex vitro storage period, 24 h treatment with bromoethane vapor (from 0.22 ml liquid BE per L volume) or bromoethane vapor followed by a 3 d treatment of 60% CO2/ 20% O2/ 20% N2 resulted in a rapid dormancy release of freshly harvested microtubers. These dormancy-releasing treatments significantly increased minituber yields under greenhouse conditions for all cultivars when compared to untreated controls. Increased minituber yields were also observed when dormancy release treatments were applied to microtubers after storage at 6 C for 8 weeks. The results demonstrate that microtuber dormancy duration can be manipulated during growthin vitro orex vitro. However, optimization may require cultivarspecific protocols