首页 | 本学科首页   官方微博 | 高级检索  
     检索      

激素对水仙组培苗生根的影响
引用本文:崔文山,周威,罗凤霞,孙晓梅,杨春起,杨怀柳,杨文吉,左静兰.激素对水仙组培苗生根的影响[J].安徽农业科学,2008,36(18).
作者姓名:崔文山  周威  罗凤霞  孙晓梅  杨春起  杨怀柳  杨文吉  左静兰
作者单位:1. 沈阳农业大学林学院,辽宁沈阳,110161
2. 金陵科技学院园艺学院,江苏南京,210038
3. 北京盛斯通生态科技有限公司,北京
4. 沈阳市园林建设工程处,辽宁沈阳,110015
5. 沈阳市绿化工程公司,辽宁沈阳,110005
基金项目:北京市园林绿化局重点项目
摘    要:目的]确定水仙组培苗小鳞茎生根诱导的适宜激素种类和水平。方法]以水仙栽培品种Fortissimo的组织培养小鳞茎为试验材料,以1/2MS为基本培养基,设计1.0、0.5、0.10、.05 mg/L 4个NAAI、BA浓度,研究激素对水仙组培苗生根诱导的影响。结果]添加0.1mg/L NAA或0.1 mg/L IBA培养基处理的小鳞茎根生长健壮,生根诱导率高,与其他处理存在显著差异(P<0.05);添加0.05 mg/L IBA处理的根生长比较细短;添加1.0 mg/L NAA或0.5 mg/L IBA处理的小鳞茎生长较快,但对根的诱导效果不明显。结论]在1/2MS培养基中,加入0.1 mg/L NAA或0.1 mg/L IBA均对水仙组培苗的生根诱导有显著促进作用。

关 键 词:水仙  离体培养  生根  激素

Effects of Hormone on the Rooting of Tissue Culture Seedlings in Narcissus
CUI Wen-shan et al.Effects of Hormone on the Rooting of Tissue Culture Seedlings in Narcissus[J].Journal of Anhui Agricultural Sciences,2008,36(18).
Authors:CUI Wen-shan
Abstract:Objective] The research aimed to confirm the suitable hormone kinds and level for rooting induction of bulblet in tissue culture seedlings of narcissus.Method] Using the tissue cultured bulblet of narcissus cultivar Fortissimo as tested materials,with 1/2MS as the basic medium,4 concn.of NAA and IBA including 1.0,0.5,0.1 and 0.05 mg/L were set up to study the effects of hormone on rooting induction of tissue culture seedlings in narcissus.Result] The root of bulblets treated by the medium with adding 0.1 mg/L NAA or 0.1 mg/L IBA grew strongly with high rooting induction rate,which had significant difference with that of other treatments(P<0.05).The root in the treatment of adding 0.05 mg/L IBA was shorter and slimmer.The bulblets in the treatments of adding 1.0 mg/L NAA or 0.5 mg/L IBA grew faster,but its induction effect on the root was not obvious.Conclusion] Adding 0.1 mg/L NAA or 0.1 mg/L IBA to 1/2 MS medium both had the significant promotion on the rooting induction of tissue culture seedlings in narcissus.
Keywords:Narcissus  In vitro culture  Rooting  Hormone
本文献已被 CNKI 维普 万方数据 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号