南京林业大学学报(自然科学版) ›› 2005, Vol. 48 ›› Issue (04): 117-119.doi: 10.3969/j.jssn.1000-2006.2005.04.028

• 研究简报 • 上一篇    下一篇

毛竹慢性枯萎病病原鉴定

史红霞1,王国良2*   

  1. 1. 浙江宁波鄞州区农林局, 浙江 宁波 315040; 2. 浙江万里学院, 浙江 宁波 315100
  • 出版日期:2005-08-18 发布日期:2005-08-18

Identification of Pathogen of Moso Bamboo Chronic Wilt

SHI Hong-xia1, WANG Guo-liang2*   

  1. 1. Agricultural and Forestry Office of Yinzhou Distriet, Ningbo 315040, China; 2. Zhejiang Wanli University, Ningbo 315100, China
  • Online:2005-08-18 Published:2005-08-18

摘要: <正>以44个银杏主要栽培品种为材料,应用ISSR分子标记为手段、,利用5个标记所产生的16个多态位点绘制这44个银杏栽培品种的ISSR指纹图谱,对这44个栽培品种进行了区分,并结合RAPD分子标记对该栽培群体的遗传多样性进行了研究。结果表明:ISSR所估算出的平均有效等位基因数目、基因多样度和shannon指数分别为1.7307,0.4101和0.5963,而RAPD所估算出的值分别为1.5735,0.333I和0.4979,说明该群体有较高的遗传多样性。ISSR技术在估算银杏遗传多样性时较RAPD更为精确。

Abstract: Based on the 3 years observation of Phyllostachys edulis infected by chronic wilt disease, the pathogen was isolated purified and indentified. The result showed that the pathogen of moso bamboo chronic wilt was Gliocladium sp.. Its primary conidiophore was Vertreillium-type braches, 96~128λm tall, phiaides in whorls of 4~5, secondary, pericillate conidiophores,stipes 64~128μm tong,phiaides(6.4~9.6)μm×(4.0~4.8)μm; the dimensions of conidia was (2.4~6.2)μmX (1.9~3.2)#m.

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