Abstract.
This study reports on the first use of a vitrification procedure for the successful cryopreservation of embryogenic cultures of a coniferous species. Using Picea mariana embryogenic cultures, we obtained the highest survival by first preculturing embryogenic masses on semi-solid medium containing 0.8 M sorbitol for 48 h followed by incubation in PVS2 cryoprotective vitrification solution at 0°C for 30 min and direct immersion in liquid nitrogen. The replacement of sorbitol with 1.6 M glycerol also resulted in high survival. When sorbitol and glycerol were used in preculture treatments, 9 of 11 embryogenic lines survived liquid nitrogen treatments. We also demonstrated that 100% post-liquid nitrogen survival of mature somatic embryos could be obtained without pretreatments. A brief desiccation pretreatment, however, increased uniformity of somatic embryo germination.
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Touchell, .D., Chiang, .V. & Tsai, .CJ. Cryopreservation of embryogenic cultures of Picea mariana (black spruce) using vitrification. Plant Cell Rep 21, 118–124 (2002). https://doi.org/10.1007/s00299-002-0490-8
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DOI: https://doi.org/10.1007/s00299-002-0490-8
- Cryopreservation Vitrification Picea mariana Somatic embryogenesis