Sugarbeet (Beta vulgaris L.) somatic embryos of biotech clone REL-2, obtained from callus grown with absci sic acid, were encapsulated with 2 % alginate and sub sequently germinated and converted into plantlets, in initial efforts necessary for eventual routine produc tion of artificial seeds. Factors examined were embryo size, alginate companion solution, cold storage dura tion, and germination substrate. Unencapsulated so matic embryo length category (0.5-1.9,2.0-2.9, or 3.0 3.9 mm) did not affect germination (98,99, 100%) or conversion (87, 89, 87%, respectively) rates into com plete plantlets on hormone-free Murashige-Skoog (MS) medium. Alginate companion solutions (either hor mone-free MS medium or H 20) had no differential ef fect on germination rate (100%) but did differ in con verting embryos to plantlets (81 vs. 64%, respectively). Subsequent experiments examining duration of cold storage of encapsulated embryos at 4°C found no lower rate of conversion at 25°C after 21 days of cold com pared with unstored embryos, but after 64 days of cold, the germination and conversion rates (70 and 45 %, respectively) at 25°C of embryos encapsulated with alginate in MS medium were lower compared with unstored embryos. With alginate in H20, germination after 64 days of storage at 4°C was 60%, and conver
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