摘要
[ Objectlve] The aim of this study was to explore an explants induction method for L. cubeba. [ Method ] Different types of L. cubeba stem segments were collected at different time as explants materials for induction and culture. [ Result ] The results showed that sterilization with 0. 1% HgC12 for 10 min achieved better effects, with an explants contamination rate of dO. 0% and a mortality rate of 15.0% ; stem segments of the 2na -5th buds below the terminal bud were better explants materials for initial induction; the best sampling time was January, with an induction rate as high as 81.1%, while the contamination rate was only 11.7% ; modified MS ＋ 1.0 mg/L of 6-BA ＋ 0.2 mg/L of NAA was the optimal medium for explants induction of L. cubeba. [ Conclusion] Semi-lignified stem segments of L cubeba collected in January, sterilized with 0.1% HgCI2 for 10 min and cultured in modified MS ＋ 1.0 mg/L of 6-BA ＋ 0.2 mg/L of NAA a- chieved better induction effects on L. cubeba seedlings.
[ Objectlve] The aim of this study was to explore an explants induction method for L. cubeba. [ Method ] Different types of L. cubeba stem segments were collected at different time as explants materials for induction and culture. [ Result ] The results showed that sterilization with 0. 1% HgC12 for 10 min achieved better effects, with an explants contamination rate of dO. 0% and a mortality rate of 15.0% ; stem segments of the 2na -5th buds below the terminal bud were better explants materials for initial induction; the best sampling time was January, with an induction rate as high as 81.1%, while the contamination rate was only 11.7% ; modified MS ＋ 1.0 mg/L of 6-BA ＋ 0.2 mg/L of NAA was the optimal medium for explants induction of L. cubeba. [ Conclusion] Semi-lignified stem segments of L cubeba collected in January, sterilized with 0.1% HgCI2 for 10 min and cultured in modified MS ＋ 1.0 mg/L of 6-BA ＋ 0.2 mg/L of NAA a- chieved better induction effects on L. cubeba seedlings.
