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日本晚樱组培快繁技术研究
引用本文:孟月娥,李艳敏,赵秀山,王慧娟.日本晚樱组培快繁技术研究[J].中国农学通报,2006,22(10):264-264.
作者姓名:孟月娥  李艳敏  赵秀山  王慧娟
作者单位:河南省农科院园艺所,郑州,450002
摘    要:进行了日本晚樱的组培快繁试验。试验结果表明,日本晚樱最佳的增殖培养基是MS/ML + 6-BA 0.5 mg/L + NAA0.05 mg/L +白糖40g/L +琼脂4.5g/L,增殖系数为2.47~2.56;最佳生根培养基为ML+IBA0.05mg/L +NAA0.05 mg/L +白糖20g/L +琼脂4.5g/L,生根率为100%;炼苗12~17d后移栽至草炭土中,成活率达90%。

关 键 词:日本晚樱  组织培养  增殖  生根
收稿时间:2006-06-28
修稿时间:2006-06-282006-07-06

Tissue Culture and Rapid Propagation of Prunus lannesiana Wils.
Meng Yue'e,Li Yanmin,Zhao Xiushan,Wang Huijuan.Tissue Culture and Rapid Propagation of Prunus lannesiana Wils.[J].Chinese Agricultural Science Bulletin,2006,22(10):264-264.
Authors:Meng Yue'e  Li Yanmin  Zhao Xiushan  Wang Huijuan
Institution:Institute of Horticulture, Henan Academy of Agriculture Science, zhengzhou 450002
Abstract:The tissue culture and rapid propagation of Prunus lannesiana Wils was studied in this paper.The results showed that the optimum medium for propagation was MS/ML + 6-BA0.5mg/L + NAA 0.05mg/L + sugar 40g/L + agar 4.5 g/L, and the ratio of proliferation was 2.47~2.56;Shoots were rooted on the medium ML + IBA 0.05 mg/L + NAA 0.05 mg/L +sugar20g/L +agar4.5g/L,and the rooting rate was 100%;Being acclimatized for 12~17d,the rooted plantlets were transplanted to turfy-soil ,the survival rate was 90%.
Keywords:Prunus lannesiana Wils    Tissue culture  Propagation  Rooting
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