%0 Articles %T Improved propagation efficiency in a laboratory–nursery interface for somatic embryogenesis in Norway spruce %A Tikkinen, Mikko %D 2018 %J Dissertationes Forestales %V 2018 %N 265 %R doi:10.14214/df.265 %U http://dissertationesforestales.fi/article/10064 %X
The aim of this work was to improve the protocol of somatic embryogenesis (SE) and propagation efficiency in Norway spruce (Picea abies (L.) Karst.), which would enable the integration of SE into Finnish breeding programme and the nursery practices applied to seedlings. The studies specifically investigated the following three areas: i) how maturation, cold storage, germination and growing conditions (laboratory–nursery interface) affect the survival and height growth of emblings (Papers I and II); ii) how to improve the efficiency of embling production from genotypes from wide genetic backgrounds (Papers I and II); and iii) how to increase propagation efficiency by rooting cuttings from emblings, and produce field testing material by combining SE and the rooting of cuttings (Papers II and III). To evaluate the possibility of improving the efficiency of SE in the laboratory–nursery interface, a series of experiments were conducted. The cost structure of SE, and the effects of improvements on costs, was estimated.
As a result, the protocol improvements doubled the yield of cotyledonary embryos, nearly doubled embling survival, and increased the height growth of emblings in the nursery by so much that sufficient planting height was reached one year less than before. Emblings were also obtained from 356 genotypes (50% thawed), and embling cuttings rooted well in conditions similar to those used for seedling cuttings. The protocol improvements also reduced embling production costs by 75%. Based on this work, emblings may be grown in nurseries after one week of in vitro germination, without any measures that differ from seedlings after transplanting. Propagation efficiency may be further increased by rooting embling cuttings. Furthermore, large-scale clone testing can be initiated with 5–12 emblings acting as cutting donors.