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不同成花量金花茶花果期果枝叶内源激素的变化
引用本文:孙红梅,廖浩斌,刘盼盼,杨 雪,李吉涛,漆小雪.不同成花量金花茶花果期果枝叶内源激素的变化[J].广西植物,2017,37(1):1537-1544.
作者姓名:孙红梅  廖浩斌  刘盼盼  杨 雪  李吉涛  漆小雪
作者单位:广西喀斯特植物保育与恢复生态学重点实验室,广西壮族自治区中国科学院 广西植物研究所,广西 桂林541006
基金项目:广西科学研究与技术开发计划项目(桂科能1598025 49);广西林业科技项目(桂林科字 [2012]第26号和 [2015]第26号)[Supported by Guangxi Science Research and Technology Development Program (1598025 49); Guangxi Forestry Science and Technology Program ([2012] No. 26 and [2015] No. 26)]。
摘    要:该研究采用ISSR分子标记,对黄枝油杉7个自然种群的遗传多样性进行了分析。结果表明:用12条ISSR引物对218个黄枝油杉个体进行扩增,共扩增出125个位点。在物种水平上,多态性位点百分数( PPL)为100.00%,Shannon信息多样性指数( I)为0.4177,Nei’ s基因多样性指数( H)为0.2666;在种群水平上,多态性位点百分数(PPL)在71.20%~92.00%之间,平均值为80.69%,Shannon信息多样性指数(I)在0.3273~0.3886之间,平均值为0.3548,Nei’ s基因多样性指数( H)在0.2139~0.2478之间,平均值为0.2291。这说明黄枝油杉在物种水平和种群水平上均显示出较高的遗传多样性。 Nei’ s遗传多样性分析( Gst=0.1433)和AMOVA分析(Φst=17.91%)表明,黄枝油杉的遗传变异主要存在于种群内,种群间的遗传分化程度较低,种群间保持一定的基因交流( Nm=2.9890>1)。 Mantel分析显示,黄枝油杉种群间的遗传距离和地理距离之间不存在显著的相关关系( r=0.4567, P=0.0610>0.05)。

关 键 词:黄枝油杉  ISSR分子标记  遗传多样性  遗传结构  保护策略
收稿时间:2017/5/11 0:00:00
修稿时间:2017/6/8 0:00:00

Dynamic changes of endogenous hormones in fruit branch leaves of Camellia nitidissima with different flower numbers during blossom and fruit periods
SUN Hong-Mei,LIAO Hao-Bin,LIU Pan-Pan,YANG Xue,LI Ji-Tao,QI Xiao-Xue.Dynamic changes of endogenous hormones in fruit branch leaves of Camellia nitidissima with different flower numbers during blossom and fruit periods[J].Guihaia,2017,37(1):1537-1544.
Authors:SUN Hong-Mei  LIAO Hao-Bin  LIU Pan-Pan  YANG Xue  LI Ji-Tao  QI Xiao-Xue
Institution:Guangxi Key Laboratory of Plant Conservation and Restoration Ecology in Karst Terrain, Guangxi Institute of Botany, Guangxi Zhuang Autonomous Region and Chinese Academy of Sciences, Guilin 541006, Guangxi, China
Abstract:In order to investigate the physical problem of flowering and fructification rate of endangered plant Camellia nitidissima, and provide the theory basis for species conservation, the contents and ratio of GA3, IAA, ZR and ABA in fruit branch leaves of C. nitidissima of more-flower, less-flower and non-flower were measured by ELISA(Enzyme-linked immunosorbent assay)method during blossom and fruit periods. In early-bloom stage, the content of IAA in leaves rised firstly and then fell, and its content of more-flower-plant was lower than that of less-flower-plant leaves; the content of ZR in flower-plant was higher than that of non-flower-plant; the content of GA3 appeared an upward trend, and its content of flower-plant was higher than non-flower-plant; the contents of ABA decreased firstly and then increased, and its content of more-flower-plant was lower than non-flower-plant. In full-bloom stage, the contents of IAA, GA3 and ABA declined overall; the content of ZR rised firstly and then fell; the contents of IAA, ZR, GA3 in more-flower plant were higher than those in less-flower-plant or non-flower-plant, while the content of ABA was less than that of other plants. During the bloom period, the ratio of IAA/ZR, IAA/ABA, ZR/ABA and GA3/ABA of flower-plant were higher than that of non-flower-plant, but the ratio of(IAA+GA3)/ZR was just in contrast, which also indicate the development of flower and fruit was related to not only single plant hormone but also the balance of plant hormones. During autumn shoot period with active vegetative growth, the ratio of IAA/ZR of non-flower-plant was larger than that of flower-plant, while the ratio of IAA/ZR of non-flower-plant was smaller in blossom and fruit period with vigorous reproductive growth, but the ratio of(IAA+GA3)/ZR was just in contrast. The results showed that high level of IAA, ABA, ZR and low level of GA3 in bud stage was benefitial for blossom, high content of IAA, ZR and low content of GA3, ABA in post-bloom stage was conducive to reducing blossom and fruit dropping, increased fruit-bearing rate and promoting fruit rapid growth, high ABA content before harvesting was favorable toward fruit ripening. Therefore, it can provide theoretical reference for using plant growth regulator to reduce the fallen petal and fruit abscission in production of C. nitidissima.
Keywords:Keteleeria calcarea  ISSR markers  genetic diversity  genetic structure  conservation strategy
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