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11.
栗疫病致病性研究和栗疫菌混合体系探讨   总被引:2,自引:0,他引:2  
经过10余年栗疫病发生特点和致病性的大量调查研究,结果表明栗疫菌在板栗分布区普遍存在,是弱寄生菌,在本地只寄生那些生长十分衰弱,即将死亡的板栗树干,苗木等,但栗疫菌的寄生不是这些部位死亡的主要和直接原因,而且它所寄生的部位局部死亡后对整株栗树的影响不大,因此,栗疫病在一般情况下非毁灭性病害,本文首次提出了栗疫菌混合体系概念,并用此说明中国栗疫病普遍分布,危害很轻的原因。  相似文献   
12.
Endothia gyrosa is a canker pathogen best known as the causal agent of pin oak blight in North America, and causes cankers on other woody hosts such as Castanea spp. and Liquidambar spp. In South Africa, Australia and Tasmania, a fungus identified as E. gyrosa has been recorded on Eucalyptus spp. Some morphological differences exist between the North American fungus and the isolates from Eucalyptus . Phylogenetic relationships between E. gyrosa from North America and E. gyrosa from South Africa and Australia, as well as that of the related fungi Cryphonectria parasitica and C. cubensis , were studied using PCR-based restriction fragment length polymorphism (RFLP) and sequences of the internal transcribed spacer (ITS) region of the rRNA operon. Endothia gyrosa isolates from South Africa produced the same RFLP banding patterns as those from Australia, which differed markedly from North American isolates of E. gyrosa . In a phylogram based on the DNA sequences, the Australian and South African isolates of E. gyrosa resided in a single, well resolved clade, distinct from North American isolates. Isolates of C. parasitica grouped in the same clade as the South African and Australian isolates of E. gyrosa , but C. cubensis was distantly related to them. The molecular data suggest that the E. gyrosa isolates from South Africa and Australia represent a distinct taxon, and probably belong to the genus Cryphonectria .  相似文献   
13.
The diversity of vegetative compatibility (vc) types and mating type was estimated in populations of the chestnut blight fungus, Cryphonectria parasitica , throughout Macedonia and from selected areas in Greece. Nearly all of the 786 isolates (94%) from Macedonia were in a single vc type, EU-12; all 379 isolates from Greece were EU-12. Only six of 20 populations in Macedonia had more than one vc type. The diversity of vc types in the most diverse populations of Macedonia was comparable with the least diverse populations found previously in Italy. All but six of the 313 isolates assayed had the same mating type, MAT-1 , and no perithecia of Cryphonectria parasitica were observed in any population. These results lead to the conclusion that sexual reproduction does not occur in these populations. The lack of vc type diversity may indicate a high potential for the spread of hypoviruses and successful biological control with transmissible hypovirulence. However, if sexual reproduction should occur in Macedonian populations, up to 32 vc types would be possible by recombination among vegetative incompatibility loci.  相似文献   
14.
栗疫菌弱毒力的转化及转化菌株的毒力测定   总被引:1,自引:0,他引:1  
采用配对转化和室内、大田接种的方法研究栗疫菌低毒力的传递和生防潜力。从12个配对菌株中得到了6个转化菌株,不同的dsRNA供体菌和受体菌配对转化的效率不同,转化率从0到100%不等。室内枝段接种和大田接种测定的毒力表明,6个转化菌株、12个供体菌株、6个不能转化的受体菌+供体菌、6个转化菌株+供体野生型菌株处理的相对毒力都在80%以下,4者之间没有显著性差异,比12个受体菌和12个供体野生型菌株的毒力都低,表现弱毒力或中等毒力。前4者与后2者的差异都达到极显著水平,而供体野生型菌株的毒力(相对毒力72.73%-108.69%)与受体菌的毒力差异不显著。实验表明低毒力菌株的生防潜力比预期的高。  相似文献   
15.
自 2 0世纪 6 0年代发现栗疫病 (干枯病 )弱毒菌系以来 ,关于弱毒菌系的研究不断深入。本文阐述了弱毒因子的传递方式、机理 ,强、弱毒菌系混合体系 ,两类菌丝的超微结构以及生理特性。栗疫菌弱毒菌系在自然界的传播受诸多因素的影响 ,弱毒菌株菌丝生长较慢 ,产孢能力较低 ,因而同强毒力菌系竞争的能力较弱  相似文献   
16.
低毒病毒-板栗疫病菌组合是研究病毒与宿主相互作用的一个优秀的模式系统。我们构建了含绿色荧光蛋白基因gfp的载体pCPXHY2GFP与含红色荧光蛋白基因rfp的载体pCPXG418RFP,并用于转化野生型菌株EP155,获得了以潮霉素为筛选标记、表达绿色荧光蛋白的转化株pCPXHY2GFP/EP155和以G418为筛选标记、表达红色荧光蛋白的转化株pCPXG418RFP/EP155。将载体pCPXG418RFP转化pCPXHY2GFP/EP155,获得的转化株能观察到绿色荧光蛋白与红色荧光蛋白共定位的现象。板栗疫病菌绿色荧光与红色荧光共定位载体pCPXHY2GFP与pCPXG418RFP的构建,为深入研究病毒与宿主相互作用的分子机制提供了强有力的研究材料。  相似文献   
17.
栗疫病是一种严重危害栗属植物的病害。为了明确栗疫病菌侵染板栗枝条的过程及侵染的关键时间点,本研究利用病理组织切片技术、显微镜和扫描电镜技术对栗疫病菌侵染板栗枝条的过程进行了观察。结果表明:接种栗疫病菌后0~5 h,菌丝先降解枝条表皮,进行横向营养生长的同时沿着伤口纵向侵染,为进入皮层做准备;接种后6 h病菌开始在表皮定殖,并侵入皮层;接种后9 h在皮层可观察到侵染性菌丝沿着细胞间隙向相邻细胞延伸;接种后12 h栗疫病菌侵入韧皮部,在皮层的侵染面积扩大。随着侵染程度加深,皮层、韧皮部等处细胞被菌丝降解,最终在形成层附近聚集。接菌后9 h为栗疫病菌侵染板栗枝条的关键时间点。  相似文献   
18.
p29蛋白是低毒病毒基因组编码的一个木瓜蛋白酶样蛋白。前人研究发现,在宿主板栗疫病菌(Cryphonectria parasitica)体内表达p29,会引起真菌毒力降低,色素产生减少,丧失产生无性孢子的能力。除已知p29与源于高尔基体的膜结构共分离之外,p29在细胞内的其它分布形式未明。本研究在成功制备p29特异抗体和高效分离板栗疫病菌线粒体的基础上,尝试用p29抗体检测线粒体中是否存在p29蛋白。Western印迹结果表明,受CHV1-EP713感染的EP713菌株线粒体中存在与p29抗体特异作用的病毒蛋白。本研究结果暗示,低毒病毒蛋白p29可能参与调控宿主线粒体功能。  相似文献   
19.
A comprehensive study of the population biology of Cryphonectria parasitica , the causal agent of chestnut blight, is required to understand the spread of the epidemic in Europe and its natural regulation by the Cryphonectria hypovirus-1 (CHV-1). With this objective in mind, the diversity in vegetative compatibility (vc) types and mating types of C. parasitica populations was assessed in 43 chestnut sites in western France and northern Spain. Isolates were sampled in three regions along the Pyrénées mountains (Hautes Pyrénées, Pyrénées Atlantiques and Navarra) and in two regions north of the Pyrénées (Landes and Dordogne). There were 61 vc types observed in 682 isolates sampled. Ninety-five isolates (14%) could not be assigned to any one of the previously known European vc types. The finding of 47 incompatible vc types confirmed that the genetics of vegetative compatibility could not be totally accounted for by six diallelic vic genes. The two idiomorphs of the mating type gene were detected in all regions, indicating that sexual reproduction could occur within and between vc types. In all regions except Dordogne, C. parasitica populations were dominated either by the vc type EU-66 or EU-72. Neither vc type has been reported elsewhere in Europe, which suggests that two different introductions of C. parasitica have occurred in the study area. In Dordogne, populations were dominated by EU-33 and EU-2, and to a lesser extent EU-66 and EU-72. The low diversity in vc types for most of the C. parasitica populations provides good opportunities for natural regulation in forest coppices and for biocontrol with CHV-1 in orchards.  相似文献   
20.
寄生隐丛赤壳菌是引起板栗疫病的致病菌。为建立该菌的分子检测技术,本研究首先采用通用引物 ITS1/ITS4对分离自四川雅安、泸州及重庆的寄生隐丛赤壳菌及其他参试菌株的 ITS 区进行 PCR 扩增和测序比对。根据该片段与 GenBank 中隐丛赤壳属其他种的 ITS 序列差异,设计了寄生隐丛赤壳菌的特异性引物 ITSP1/ITSP2,片段扩增大小为462 bp。利用该引物对菌株基因组 DNA 进行扩增,可以将寄生隐丛赤壳菌与其他参试菌区分开,检测灵敏度达30 pg。而以引物 ITS1/ITS4和 ITSP1/ITSP2进行的巢氏 PCR,可检测到30 fg 基因组 DNA,其灵敏度较常规 PCR 提高了1000倍。利用巢氏 PCR 检测体系对发病程度不同的组织和携菌组织进行检测,均能快速稳定地检测出寄生隐丛赤壳菌。  相似文献   
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