Cryopreservation of yams using vitrification modified by including droplet method: effects of cold acclimation and sucrose.

Cryopreservation of yams (Dioscorea spp.) is important for the preservation of valuable genotypes for food, medicine and breeding purposes. This study on four species of yams was conducted to evaluate the influence of cold acclimation in an alternating 5 degree C and 28 degree C, 12 h thermo-photo-period and of two sucrose concentrations in the preculture medium using a modified droplet method. Acclimation of a 3-week period provided the best preconditioning treatment averaged over four genotypes. Effect of sucrose concentration in the preculture medium depended on the genotype (significant genotype x sucrose interaction; P = 0.036). High survival (67 to 70%) with 30% to 50% shoot recovery was obtained for D. bulbifera, D. polystachya and D. cayenensis, compared to 20 percent survival without shoot recovery for D. alata.

Investigating a new cryopreservation protocol for yams ( Dioscorea spp.).

Experiments were initiated to develop protocols for four species of Dioscorea, namely D. bulbifera L., D. oppositifolia L., D. alata L. and D. cayenensis Lam., and to assess the effects of various factors on the survival and regrowth of explants after rewarming. The treatments consisted of three different methods-vitrification, droplet and a modified droplet method-as well as the following variables-cryoprotective solution, sucrose concentration in the preadaptation medium and cold acclimation. While most of the protocols resulted in low to zero survival and regrowth rates, maximum survival rates of 100% and 75% were obtained for D. oppositifolia L. and D. cayenensis Lam., respectively, using two different protocols of the modified droplet method. A higher average survival rate was obtained using the droplet and modified droplet techniques than for the original vitrification methods. When the average of all the experiments was taken, more than one-half (52%) of the surviving explants developed further within 1 month with the modified droplet method compared to zero regrowth with the two other methods. The optimum protocol for cryopreservation is specific for each genotype.