The unfertilized ovules of one clone of Gerbera jamesonii H. Bolus ex Hook. f. were cultured in vitro as a means of producing haploid plants. A total of 4715 ovules were cultivated on 17 media during two distinct periods of the year. All the media tested, except the ones containing 0.5% w/v of activated charcoal, were able to sustain the formation of callus. When these calli were transferred to the regeneration medium, shoot differentiation occurred in about 2 weeks. Usually, callus induction occurred at a higher frequency during the fall experiments. However, the calli produced in the spring displayed a higher morphogenetic capacity. Chromosome and chloroplast counts performed on randomly selected plants revealed that 76% of the regenerants were haploid and 24% were diploid.
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