全文获取类型
收费全文 | 1295篇 |
免费 | 93篇 |
国内免费 | 51篇 |
专业分类
林业 | 34篇 |
农学 | 135篇 |
29篇 | |
综合类 | 519篇 |
农作物 | 161篇 |
畜牧兽医 | 5篇 |
园艺 | 67篇 |
植物保护 | 489篇 |
出版年
2024年 | 2篇 |
2023年 | 19篇 |
2022年 | 32篇 |
2021年 | 21篇 |
2020年 | 30篇 |
2019年 | 29篇 |
2018年 | 42篇 |
2017年 | 31篇 |
2016年 | 60篇 |
2015年 | 51篇 |
2014年 | 37篇 |
2013年 | 48篇 |
2012年 | 82篇 |
2011年 | 94篇 |
2010年 | 64篇 |
2009年 | 84篇 |
2008年 | 82篇 |
2007年 | 93篇 |
2006年 | 63篇 |
2005年 | 72篇 |
2004年 | 41篇 |
2003年 | 50篇 |
2002年 | 41篇 |
2001年 | 56篇 |
2000年 | 28篇 |
1999年 | 30篇 |
1998年 | 28篇 |
1997年 | 18篇 |
1996年 | 14篇 |
1995年 | 17篇 |
1994年 | 10篇 |
1993年 | 17篇 |
1992年 | 9篇 |
1991年 | 13篇 |
1990年 | 10篇 |
1989年 | 9篇 |
1988年 | 3篇 |
1987年 | 3篇 |
1985年 | 1篇 |
1982年 | 1篇 |
1980年 | 2篇 |
1979年 | 1篇 |
1978年 | 1篇 |
排序方式: 共有1439条查询结果,搜索用时 15 毫秒
1.
为了解决马铃薯致病疫霉侵染马铃薯导致其死亡,进而造成马铃薯单位种植产量低的问题。本文从拮抗菌入手,归纳分析细菌类拮抗菌中的主要拮抗菌中芽孢杆菌、假单胞菌和粘细菌对马铃薯致病疫霉的抑制作用。同时,在总结前人研究的基础上,笔者认为在拮抗菌应用方面,可以采用多对一的新型平板对峙筛菌模式来模拟复杂条件下拮抗菌的拮抗作用,以期得到稳定的拮抗菌;并指出应从定植能力和根际微生物影响方面对拮抗菌实际应用的可行性进行研究;此外,提出未来对拮抗菌抑制马铃薯致病疫霉的探究应从表型层面的研究深入到分子层面,以期能成功从源头找寻抑制马铃薯致病疫霉的答案。 相似文献
2.
烟草黑胫病菌(Phytophthora parasitica var. nicotianae)生理小种鉴定技术研究 总被引:1,自引:0,他引:1
在1980-1986年,对烟草黑胫病菌生理小种鉴定技术和方法进行了研究和探讨。结果表明,Nicotiana ncsophil(?),Burley21;Burley37;N.stocktonii是理想的鉴别寄主:整株接种方法优于其他的接种方法;接种物浓度以控制在相同的水平(10~3 ml)为宜。为减小生物测定的差异,所有菌系应一次完成测定。 相似文献
3.
据1981~1983年9个哈密瓜生产基地根颈部病害的病原成份调查表明,哈密瓜疫病的优势种为掘氏疫霉菌(Phytophthora drechsleri Tucker.)。为澄清在新疆掘氏疫霉的寄主范围,1989~1990年用1981年采自鄯善县哈密瓜上分离的单孢(Phy-6)菌株,在温室平均温度25~28℃条件下对5科25种自然根颈感病的栽培作物作接种试验。结果表明,本菌是葫芦科大多数作物的重要致病菌,并可侵染棉花和红花;在有伤口条件下可以侵染南瓜、西葫芦和茄株;对苦瓜、丝瓜,豆科作物的豇豆、四季豆、菊科的向日葵、茄科的蕃茄、辣椒、烟草、马铃薯、蔷薇科草莓(植株)等均不能致病。 相似文献
4.
棉铃疫病是长绒棉铃期的重要病害,在新疆阿拉尔地区,七月底至八月上旬,若遇低温、阴雨、高湿的环境条件也能严重流行。种植抗病品种和改善生态因素是控制病害发生和流行的重要途径。 相似文献
5.
Thomas Thomidis 《Phytoparasitica》2002,30(2):191-193
The virulence ofPhytophthora citrophthora isolated from various host-plants on three peach rootstocks (GF677, PR204, KID I) was examined. There was no significant
difference among the rootstocks with respect to their susceptibility to testedP. citrophthora isolates. The most virulent isolate originated from sycamore (Acer pseudoplatanus); isolates from pistachio trees (Pistacia vera) also showed high virulence but were significantly less virulent than the sycamore isolate. Isolates originating from plum
(Prunus domestica), almond (Prunus amygdalus) and lemon (Citrus limon) trees were moderately virulent on peach rootstocks; those from cyclamen (Cyclamen persicum) showed the lowest virulence of those tested. There was thus great variation in virulence among the testedP. citrophthora isolates. It is possible that the isolates ofP. citrophthora from sycamore, pistachio, plum, almond and lemon trees are a threat to peach trees, whereas the low virulence of the isolates
from cyclamen hosts suggests that these pathogens are not a serious threat to peach trees.
http://www.phytoparasitica.org posting Jan. 3, 2002. 相似文献
6.
辣椒疫病发病主导因素及综合防治技术研究 总被引:2,自引:0,他引:2
通过3a在多年辣椒重茬地的田间试验及调查研究,基本明确了辣椒疫病发生与灌水方法、栽培方式、降水、中心病株的出现等主导因素的关系。提出了栽培防病、化学治疗的综防技术,达到控病增产的目的。 相似文献
7.
β- 氨基丁酸诱导甜( 辣) 椒抗疫病作用的研究 总被引:12,自引:2,他引:12
报道了用β- 氨基丁酸( DL-β-aminon-butyric acid, BABA) 喷雾处理辣椒叶片和茎后的诱导抗疫病作用。研究证明: 高浓度BABA ( 1 000 g/mL) 对离体辣椒疫霉病菌无抗菌活性, 用其喷雾处理辣椒的茎叶所诱导的抗疫病作用可完全控制其危害; 用BABA 诱导处理后3 d 接种辣椒疫霉病菌, 辣椒植株开始表达出较高的诱导抗性, 这种抗病作用可持续20 d 以上, 并表现出与数量抗病性相似的特性。 相似文献
8.
Genetic variation among asexual progeny of Phytophthora infestans detected with RAPD and AFLP markers 总被引:6,自引:1,他引:6
Genotypic variation among 32 single-zoospore isolates (SZI) of Phytophthora infestans , derived asexually from two hyphal-tip parental isolates (PI-105 and PI-1) of the US-8 genotype, was assessed with 80 random amplified polymorphic DNA (RAPD) primers and 18 amplified fragment length polymorphic DNA (AFLP) primer pairs. In previous investigations, the SZIs from parental isolate PI-105 showed high levels of virulence variability and were differentiated into 14 races, whereas the SZIs from PI-1 showed identical virulence to the parent. The purpose of this investigation was to determine if phenotypic variation observed among SZIs of P. infestans could be detected at the DNA level in these isolates. Polymorphism was detected with 51 RAPD primers and with all 18 AFLP primer pairs in PI-105 SZIs. In SZIs from PI-1, polymorphism was also detected with 25 RAPD primers and 17 AFLP primer pairs. Cluster analysis using the unweighted pair-group method with arithmetic averages (UPGMA) separated the SZIs from parent PI-105 into six virulence groups, 11 RAPD groups and three AFLP groups. Cluster analysis of PI-1 SZIs, which all belong to the same virulence group, differentiated them into four RAPD groups and six AFLP groups. No close correlation among RAPD, AFLP and virulence groups could be established within the two progenies of SZIs. Results of this study suggest that there is a considerable level of inherent genetic variability among SZIs derived asexually from the same parental isolate. The possible mechanisms and implications of this genetic variation are discussed. 相似文献
9.
Rapid detection of Phytophthora cinnamomi using PCR with primers derived from the Lpv putative storage protein genes 总被引:1,自引:1,他引:1
Phytophthora cinnamomi is an ecologically and economically important pathogen. In this study, PCR assays were developed with primer pair LPV2 or LPV3 for rapid detection and identification of this organism. Both primer pairs were selected from putative storage protein genes. The specificity of these primer pairs was evaluated against 49 isolates of P. cinnamomi , 102 isolates from 30 other Phytophthora spp., 17 isolates from nine Pythium spp. and 43 isolates of other water moulds, bacteria and true fungi. PCR with both primer pairs amplified the DNA from all isolates of P. cinnamomi regardless of origin. The LPV3 primers showed adequate specificity among all other species tested. The LPV2 primers cross-reacted with some species of Pythium and true fungi, but not with any other Phytophthora species. PCR with the LPV3 primers detected the pathogen at levels of a single chlamydospore or 10 zoospores in repeated tests. The PCR assay was at least 10 times more sensitive than the plating method for detection of the pathogen from artificially infested soilless medium, and, to a lesser extent, from naturally infected plants. PCR with LPV3 primers can be a useful tool for detecting P. cinnamomi from soilless media and plant tissues at ornamental nurseries, whereas the LPV2 primers can be an effective alternative for identification of this species from pure culture. Applications of these assays for detection of P. cinnamomi in other environments were also discussed. 相似文献
10.