Unlabelled: BACKGROUND: A cryopreservation protocol has been established for oil palm somatic embryos (SEs), the efficiency of which must be evaluated, both in terms of regeneration and of long-term storage capacity, before its large-scale routine use.
Objective: To test the survival and recovery of 29 clones of oil palm somatic embryos cryostored for 20 years.
Materials And Methods: Clumps of SEs were pregrown for 7 days on medium containing 0.
Cryopreservation via droplet vitrification showed high efficiency for cassava meristems (79 pecent average recovery) when these were excised from in vitro seedlings. The efficiency of the process dropped considerably (to > 23 percent) when meristems were excised from field-grown plants, thus precluding the use of such explants for routine cryobanking. In yam, large disparities were observed in the ability of meristems to produce a shoot after cryopreservation ranging from 0 to 60 percent, depending on the accession.
View Article and Find Full Text PDFIn this paper, the long term observation of plants originating from control and cryopreserved stabilized polyembryonic cultures (SPCs) of six elite oil palm clones was carried out. Survival of plantlets in the nursery was monitored, then a series of vegetative and floral characteristics of over 440 palms were studied for up to 12 years after field transfer in Côte D'Ivoire. The six clones tested showed an average recovery of 34% after freezing in liquid nitrogen.
View Article and Find Full Text PDFDSC analysis was performed at three points in the cryopreservation process on encapsulated-dehydrated meristems of Ribes ciliatum. Meristems were excised from shoots pre-treated with either sucrose or glucose, encapsulated in alginate beads, dehydrated in sucrose solutions, air dried, and plunged in liquid nitrogen. Thermal analysis revealed glass transitions during cooling of air-desiccated meristems, however, on rewarming a small endothermic event was detected suggesting glass destabilization can occur.
View Article and Find Full Text PDFThe standard cryopreservation process previously developed for oil palm clones using shiny white, finger-like somatic embryos could be applied in some cases to standard cultures. Its efficiency was markedly improved by completing the 7-day pregrowth period on 0.75 M sucrose by an additional dehydration period carried out either by placing the embryos in the air current of the laminar flow cabinet or in an air tight box containing silica gel.
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