马铃薯炭疽病研究进展

被引：7

作者：

刘会梅 ^{[1
]}

王向军 ^{[1
]}

封立平 ^{[2
]}

机构：

[1] 黄岛出入境检验检疫局

[2] 山东出入境检验检疫局技术中心

来源：

植物检疫 | 2007年 / 01期

关键词：

马铃薯炭疽病; 进展; 检测;

D O I：

10.19662/j.cnki.issn1005-2755.2007.01.019

中图分类号：

S41-30 [植物病害、虫害及杂草检疫]; S435.32 [马铃薯（土豆）病虫害];

学科分类号：

0904 ; 090401 ; 090402 ;

摘要：

马铃薯炭疽病为一种严重影响马铃薯生产的世界性病害,属我国检疫性病害。本文综述了该病的分布和危害、识别特征、病原菌的生物学特性、检测方法、检疫重要性以及防治措施等,并在此基础上提出了该病研究过程中存在的问题和展望。

引用

页码：38 / 41

页数：4

共 20 条

[1]

Effect of soil solarisation and mouldboard ploughing on black dot of potato, caused by Colletotrichum coccodes[J] . F. D. N. Denner,C. P. Millard,F. C. Wehner. &nbspPotato Research . 2000 (3)

[2] EFFICACY OF FUNGICIDES AGAINST COLLETOTRICHUM-COCCODES ON POTATO-TUBERS [J].

MARAIS, L .

POTATO RESEARCH, 1990, 33 (02) :275-281

[3] The effect of seed- and soilborne inoculum of Colletotrichum coccodes on the incidence of black dot on potatoes [J].

Denner, FDN ;

Millard, CP ;

Wehner, FC .

POTATO RESEARCH, 1998, 41 (01) :51-56

[4]

Nitazan N,Hazanovsky M,Tal M,et al.Vegetative compatibility groups inColletiotrichum coccodes,the casual agent of black dot on potato. Phytopathology . 2002

[5]

Johnson D A,Miliczky E R.Distribution and development of black dot,Verticilliumwilt,and powdery scab on Ruset Burbank potatoes in Washington State. Plant Disease . 1993

[6]

Farley J D.A selective medium for assay ofColletotrichum coccodes in soil. Phytopathology . 1972

[7]

Chesters C G C,Hornby D.Studies onColletotrichum coccodes2 Al-ternative host tests and tomato fruit inoculations using a typical tomato root isolate. Transaction of the British Mycological Society . 1965

[8]

Cullen D W,Lees A K,Toth I K,et al.Detection ofColletiotrichum coccodesfrom soil and potato tubers by conventional and quantitative real-time PCR. Plant Pathology . 2002

[9]

Tsror(Lahkim L),Erlich O,Hazanovsky M.Effect ofColletotrichum coccodeson potato yield,tuber quality,and stem colonization during spring and autumn. Plant Disease . 1999

[10]

Fagbola O,Abang M M.Colletotrichum circiansandColletotrichum coccodescan be distinguished by DGGE analysis of PCR-amplified18S rDNA fragments. African Jorunal of Biotechnology . 2004

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