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矮牵牛的快速繁殖技术
引用本文:朴日子,金英善,曹后男,宗成文,王兴国. 矮牵牛的快速繁殖技术[J]. 延边大学农学学报, 1999, 0(4)
作者姓名:朴日子  金英善  曹后男  宗成文  王兴国
作者单位:延边大学农学院果林系!吉林龙井133400
摘    要:以矮牵牛为试材,筛选了快速繁殖优良苗木时的最适基本培养基浓度及激素条件.结果表明分化培养时的最适培养基为1/4 MS+ BA0 .5 mg/L+IBA0 .02 mg/L;增殖培养时为MS+ BA0 .5mg/L+ IBA0 .2 mg/L;诱导根系培养时为1/2 MS+ IBA0 .5 mg/L+ 活性炭100 mg/L.生根培养基中添加活性炭有效地促进了矮牵牛根系的生长和发育,同时促进了叶片和茎的分化生长.

关 键 词:矮牵牛  培养基  激素

High-speed breeding technique of petunia
PIAO Ri zi,JIN Ying shan,CAO Hou-nan,ZONG Cheng wen,WANG Xing guo. High-speed breeding technique of petunia[J]. Journal of Agricultural Science Yanbian University, 1999, 0(4)
Authors:PIAO Ri zi  JIN Ying shan  CAO Hou-nan  ZONG Cheng wen  WANG Xing guo
Abstract:The basic culture medium concentration and hormones condition when breed excellent nursery stock were selected using petunia.The result shows,the excellent culture medium of differentiation culture is 1/4 MS BA 0.5 mg/L IBA 0.02 mg/L;enrichment culture is MS BA 0.5 mg/L IBA 0.2 mg/L;inducement culture is 1/2 MS IBA 0.5 mg/L active carbon 100 mg/L.Rooting medium added.
Keywords:petunia  culture medium  hormone
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