Abstract

The possibility to utilize non-additive genetic gain in planting stock has increased the interest towards vegetative propagation. In Finland, the increased planting of Norway spruce combined with fluctuant seed yields has resulted in shortages of improved regeneration material. Somatic embryogenesis is an attractive method to rapidly facilitate breeding results, not in the least, because juvenile propagation material can be cryostored for decades. Further development of technology for the somatic embryogenesis of Norway spruce is essential, as the high cost of somatic embryo plants (emblings) limits deployment. We examined the effects of maturation media varying in abscisic acid (20, 30 or 60 µM) and polyethylene glycol 4000 (PEG) concentrations, as well as the effect of cryopreservation cycles on embryo production, and the effects of two growing techniques on embling survival and growth. Embryo production and nursery performance of 712 genotypes from 12 full-sib families were evaluated. Most embryos per gram of fresh embryogenic mass (296 ± 31) were obtained by using 30 µM abscisic acid without PEG in the maturation media. Transplanting the emblings into nursery after one-week in vitro germination resulted in 77% survival and the tallest emblings after the first growing season. Genotypes with good production properties were found in all families.

Highlights

  • In Finland, the increased planting of Norway spruce

  • The increase in embryo yield was over two-fold in Trials 1 and 2 of Experiment I when the reduced amount of Abscisic acid (ABA) was compared to the control μM ABA treatment

  • Reducing the ABA concentration in the maturation media increased the yield of cotyledonary embryos

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Summary

Introduction

In Finland, the increased planting of Norway spruce Karst.) seedlings and difficulties in seed production has resulted in intermittent shortages of regeneration material of a high breeding value [1]. One solution to this problem is to use vegetative propagation, e.g., somatic embryogenesis (SE), which was observed in Norway spruce for the first time in 1985 [2,3]. The cryopreservation of embryogenic tissue (ET) in liquid nitrogen (LN) enables long-term storage of regeneration material in its juvenile state [6,7,8]. For Norway spruce, reliable cryopreservation protocols applicable for large number of samples have been developed [8,15]. Acceptable recovery rates together with high morphological and genetic fidelity have been observed [8,15]

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