| 八仙花的组织培养与快繁技术 |
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| 引用本文： | 任叔辉.八仙花的组织培养与快繁技术[J].防护林科技,2006(1):10-11. |
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| 作者姓名： | 任叔辉 |
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| 作者单位： | 河南科技大学林业职业学院,河南,洛阳,471002 |
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| 摘 要： | 以八仙花带腋芽茎段作外植体进行离体培养,通过不同灭菌剂及灭菌时间对外植体的影响,不同激素组合对外植体芽分化和生根的影响的试验研究,结果表明:较适宜的增殖培养基为MS+6-BA1.0+NAA0.2和MS+6-BA1.0+IAA0.1;生根培养基为1/2MS+IBA0.2或1/2MS+IBA0.1。
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| 关 键 词： | 八仙花 组织培养 培养基 快繁 |
| 文章编号： | 1005-5215（2006）01-0010-02 |
| 收稿时间： | 2005-06-14 |
| 修稿时间： | 2005-06-14 |
Tissue Culture and Fast Propagation Technique of Hydrangea macrophylla |
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| REN Shu-hui.Tissue Culture and Fast Propagation Technique of Hydrangea macrophylla[J].Protection Forest Science and Technology,2006(1):10-11. |
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| Authors: | REN Shu-hui |
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| Abstract: | Stems having axillary bud of Hydrangea macrophylla were used as explants to conduct in vitro culture.Through researches of the effect of different sterilant and sterilization time on explant and the effect of different hormone combinations on bud differentiation of explant and rooting,results showed that the optimum multiplication culture media were Ms+6-BA(1.0)+NAA0.2 and Ms+6-BA1.0+IAA0.1.The rootage culture medium was 1/2MS+IBA0.2 or 1/2MS+IBA0.1. |
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| Keywords: | Hydrangea macrophylla tissue culture culture medium fast propagation |
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