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[Objective] This study aimed to develop tissue culture and rapid propagation methods for pedicels of Hemerocallis hybrida.[Method] Tender pedicels of dwarf H.hybrida were used as experimental materials to select callus induction,subculture and rooting media for rapid propagation of H.hybrida.[Result] MS+2.0-3.0 mg/L 6-BA+0.2-0.3 mg/L NAA,MS+1.0-2.0 mg/L 6-BA+0.1-0.2 mg/L NAA,MS and 1/2MS+0.2 mg/L NAA were the appropriate medium for callus induction,subculture and rooting,respectively.[Conclusion] The in vitro culture and clustered seedling rooting technology used in this study are effective methods for rapid propagation of H.hybrida,which provide technical reference for industrialized production of H.hybrida.
[Objective] This study aims to develop tissue culture and rapid propagation methods for pedicels of Hemerocallis hybrida. [Method] Tender pedicels of dwarf H. hybrida were used as experimental materials to select callus induction, subculture and rooting media for rapid propagation of H. [ [Result] MS + 2.0-3.0 mg / L 6-BA + 0.2-0.3 mg / L NAA, MS + 1.0-2.0 mg / L 6-BA + 0.1-0.2 mg / L NAA, MS and 1/2 MS +0.2 mg / L NAA were the appropriate medium for callus induction, subculture and rooting, respectively. [Conclusion] The in vitro culture and clustered seedling rooting technology used in this study are effective methods for rapid propagation of H. hybrida, which provide technical reference for industrialized production of H.hybrida.