摘要: 以MS+6-BA2.0mg/L+IBA0.5mg/L为增殖培养基,1/2MS+IBA0.1mg/L为生根培养基,添加不同浓度的PP333,其结果表明:增殖培养基中添加0.1~0.5mg/L PP333对八仙花试管苗增殖和复壮均有效,而在生根培养基中添加0.05~0.5mg/LPP333有利于生根和移栽,其中以1/2MS+IBA0.1mg/L+PP3330.1mg/L培养基对八仙花试管苗生根和移栽有良好效应
邱运亮. Study on Effect of PP333 on in vitro Rapid Propagation of Hydrangea macrophylla[J]. 中国农学通报, 2005, 21(4): 56-56.
Qiu Yunliang. Study on Effect of PP333 on in vitro Rapid Propagation of Hydrangea macrophylla[J]. Chinese Agricultural Science Bulletin, 2005, 21(4): 56-56.