Abstract
Hydrangea (Hortensia) is a highly popular ornamental plant for garden decoration, and now it is commercially produced for cut flower branches. For in vitro culture, Murashige and Skoog medium supplemented with BA (0.25 mg/L) and sucrose (30 g/L) was used. Culture conditions were 23 ± 1°C of temperature, light intensity of 35 μmol/m2/s P.P.F.D., and 16/8 h day/night photoperiod. Following shoot proliferation, the in vitro rooting frequency was 100% on a medium containing NAA 0.5 mg/L. However, 95% direct in vivo rooting was achieved by dipping microcuttings in a 5,000 ppm K-IBA solution which were transferred afterward to a glasshouse for acclimatization. After 21 days, fully acclimatized and well-established plants were obtained, suitable for commercialization. Furthermore, leaf fragments derived from in vitro plantlets were cultured for callus induction and adventitious shoot regeneration.
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Acknowledgements
The results reported in this paper comes from the project “Valorizzazione a scopi commerciali del genere Hydrangea” supported by the Italian Ministry of Agriculture (D.M. I1063/7643/09) in collaboration with the CRA-VIV of Pescia, Italy, and the Company “Meristema” di Pasqualetto P.L. (Cascine di Buti, Italy).
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Ruffoni, B., Sacco, E., Savona, M. (2012). In Vitro Propagation of Hydrangea spp.. In: Lambardi, M., Ozudogru, E., Jain, S. (eds) Protocols for Micropropagation of Selected Economically-Important Horticultural Plants. Methods in Molecular Biology, vol 994. Humana Press, Totowa, NJ. https://doi.org/10.1007/978-1-62703-074-8_18
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DOI: https://doi.org/10.1007/978-1-62703-074-8_18
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