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171.
Effect of Leaf Infection by Kabatiella zeae on Stalk Rot Prevalence and Grain Yield of Maize Hybrids 总被引:1,自引:0,他引:1
Eight maize hybrids were tested for resistance to eyespot (Kabatiella zeae) and stalk rot (Fusarium spp.) under field conditions in 1993–1995. The relationship between eyespot and stalk rot and their effect on grain yield of hybrids were studied. Effectiveness of the prochloraz fungicide in controlling both diseases was evaluated. The experiments were performed in three subtrials where plants were naturally infected, inoculated with K. zeae or treated with the fungicide, Sportak 450 EC. The relationship between intensity of leaf damage by eyespot and incidence of stalk rot has been evidently confirmed. High infection of leaf by K. zeae reduced grain yield of hybrids. However, considerable differences in prevalence of disease and yield losses were noted in successive years. The intensity of eyespot depended upon environmental conditions highly variable over the years: it was enhanced by low temperature and high air humidity in July and August. Hybrids showed significant differences in susceptibility to both diseases. Mona – hybrid from the USA and two experimental hybrids from Poland were less affected by diseases than Smolimag and Hidosil (commercial hybrids from Poland). The fungicide Sportak was effective in controlling eyespot and had an indirect influence on decreasing fusarium stalk rot. 相似文献
172.
173.
Environmental fate of the triazole fungicide propiconazole in a rice-paddy-soil lysimeter 总被引:1,自引:0,他引:1
Kim In Seon Beaudette Lee A. Han Shim Jae Trevors Jack T Tack Suh Yong 《Plant and Soil》2002,239(2):321-331
Environmental fate of the triazole fungicide propiconazole, 1-[[2(2,4-dichlorophenyl)-4-propyl-1,3-diox olane-2-yl]methyl]1H-1,2,4-triazole, in soil was investigated using lysimeters simulating a rice-paddy-soil conditions. Two lysimeters composed of different soil types, a sandy loam (lysimeter A) and silty clay (lysimeter B), were used. Propiconazole (Tilt 250R EC) plus [U-14C]-propiconazole was applied over a two-year period to the soil surface of the lysimeters. Propiconazole fate in the lysimeters was assessed by measuring total radioactivity in the leachate, evolved 14CO2, and 14C-residues in the soil and rice plants. The amounts of applied 14C in the leachate from lysimeter A were 4.4 and 5.2% in the first and second year, respectively. A background level of (0.00005% of applied) 14C in the leachate from lysimeter B was detected, suggesting negligible movement of the fungicide to groundwater in the silty clay soil. The amount of 14CO2 evolved from lysimeter A accounted for 7.8 and 12.2% of applied 14C in the first and second year, respectively, whereas those from lysimeter B were 5.7 and 7.1%. Total 14C detected in the rice plants grown in lysimeter A were 7.3 and 9.8% of applied 14C in the first and second year, respectively, which compared to 3.0 and 7.6% in lysimeter B. Most of the applied 14C was detected in the top 10 cm soil layer, suggesting that propiconazole remains close to the soil surface after application in soil. Degradation products of propiconazole identified in the lysimeter soils were 1-[[2(2,4-dichlorophenyl)-2-(1,2,4-triazole -1-yl) ketone (DP-1), 1-(2,4-dichlorophenyl)-2-(1,2,4-triazole-1- yl) ethanol (DP-2) and 1-[[2(2,4-dichlorophenyl)-4-hydroxypropyl-1,3-dioxolane-2-yl]methyl]1H-1,2,4-triazole (DP-3 and DP-4). 相似文献
174.
Fei Xie Tingjunhong Ni Jing Zhao Lei Pang Ran Li Zhan Cai Zichao Ding Ting Wang Shichong Yu Yongsheng Jin Dazhi Zhang Yuanying Jiang 《Bioorganic & medicinal chemistry letters》2017,27(10):2171-2173
Twenty-nine novel triazole analogues of ravuconazole and isavuconazole were designed and synthesized. Most of the compounds exhibited potent in vitro antifungal activities against 8 fungal isolates. Especially, compounds a10, a13, and a14 exhibited superior or comparable antifungal activity to ravuconazole against all the tested fungi. Structure-activity relationship study indicated that replacing 4-cyanophenylthioazole moiety of ravuconazole with fluorophenylisoxazole resulted in novel antifungal triazoles with more effectiveness and a broader-spectrum. 相似文献
175.
Take-all and grain yields in sequences of winter wheat crops testing fluquinconazole seed treatment applied in different combinations of years 总被引:1,自引:0,他引:1
A seed treatment containing fluquinconazole as the only active ingredient was tested in sequences of up to six consecutive crops of winter wheat. It was applied or not applied in each year, and was tested in all possible combinations with treatments applied in previous years. Take‐all was controlled effectively, and grain yield usually increased, when the disease intensity was moderate or severe in non‐treated crops, but control of the most severe take‐all did not result in acceptable yields or grain quality. Treatment of a first wheat or second wheat with little take‐all did not usually benefit the subsequent crop. Non‐treatment of a crop grown after a treated, diseased crop usually resulted in a marked increase in disease, indicating that treatment had delayed progress of the epidemic. Take‐all was controlled by treatment of a crop grown after a treated, diseased crop but the amount of control and of increased yield was often less than that in a treated crop grown after a non‐treated crop in the same crop sequence. Similar effects of seed treatment were apparent in crops grown on a site with take‐all decline. The alternative fungicide, silthiofam, applied as a seed treatment in the later years of some experiments, was usually as effective as fluquinconazole. From these experiments, it is recommended that: a) fluquinconazole seed treatment should be applied to a second or third wheat crop, grown after a first wheat crop that was managed to avoid rapid take‐all development (e.g. by avoiding very early sowing); b) a break crop should follow the treated crop; c) the seed treatment should not normally be used in longer sequences of wheat or on take‐all decline soil unless it is planned to follow the treated crop with a non‐cereal break. 相似文献
176.
Brown A Brown L Ellis D Puhalo N Smith CR Wallace O Watson L 《Bioorganic & medicinal chemistry letters》2008,18(15):4278-4281
A novel series of Oxytocin antagonists are described. This series was identified through pharmacophoric overlap of in-house and literature antagonists. Subsequent optimization led to a series of potent, selective antagonists. Several analogues displayed oral bioavailability in vivo in the rat. 相似文献
177.
W. I. Golubev T. V. Kulakovskaya A. S. Shashkov E. V. Kulakovskaya N. V. Golubev 《Microbiology》2008,77(2):171-175
The yeast Pseudozyma graminicola isolated from plants inhibited growth of almost all ascomycetes and basidiomycetes tested (over 270 species of ca. 100 genera) including pathogenic species. This yeast secreted a fungicidal agent, which was identified as a glycolipid composed of cellobiose residue with two O-substituents (acetyl and 3-hydroxycaproic acid) and 2,15,16-trihydroxypalmitic acid. The release of ATP from the glycolipid-treated cells indicated that this glycolipid impaired the permeability of the cytoplasmic membrane. Basidiomycetes were more sensitive to the cellobiose lipid than ascomycetes. 相似文献
178.
小麦赤霉病是小麦上的主要病害之一,在全世界范围内引起该病害的致病菌主要是禾谷镰孢菌Fusarium graminearum。目前,使用杀菌剂是生产上防治小麦赤霉病发生和危害的主要手段,常用的杀菌剂主要有苯并咪唑类杀菌剂(benzimidazoles)等,苯并咪唑类杀菌剂的作用靶标是β2微管蛋白。本研究旨在探究小麦赤霉病菌中β2微管蛋白与苯并咪唑类杀菌剂的互作机制,通过同源建模的方法获得了禾谷镰孢菌β2微管蛋白的三维结构,并在此基础上将β2微管蛋白与4种苯并咪唑类杀菌剂(多菌灵、苯菌灵、噻菌灵、甲基硫菌灵)进行分子对接。分子对接结果显示β2微管蛋白第198位苯丙氨酸和第236位缬氨酸与4种苯并咪唑类杀菌剂直接互作形成氢键,第50、134、165、167、198、200、236、237、239、240、250、253、257、314位氨基酸形成药剂结合口袋。通过比较β2微管蛋白与4种苯并咪唑类杀菌剂结合自由能,发现与其他3种杀菌剂相比,β2微管蛋白与多菌灵的结合自由能最小(-5.72 kcal/mol),说明其与多菌灵互作亲和力更强。采用菌丝生长速率法测定了禾谷镰孢菌对4种苯并咪唑类杀菌剂的EC50值,禾谷镰孢菌对多菌灵、苯菌灵、噻菌灵、甲基硫菌灵的EC50值分别为0.772、0.862、1.088、13.266 mg/L,该结果表明禾谷镰孢菌对多菌灵的敏感性强于其他3种杀菌剂,与分子对接结果相吻合。 相似文献
180.
A new point mutation in the iron–sulfur subunit of succinate dehydrogenase confers resistance to boscalid in Sclerotinia sclerotiorum 下载免费PDF全文
Research has established that mutations in highly conserved amino acids of the succinate dehydrogenase (SDH) complex in various fungi confer SDH inhibitor (SDHI) resistance. For Sclerotinia sclerotiorum (Lib.) de Bary, a necrotrophic fungus with a broad host range and a worldwide distribution, boscalid resistance has been attributed to the mutation H132R in the highly conserved SdhD subunit protein of the SDH complex. In our previous study, however, only one point mutation, A11V in SdhB (GCA to GTA change in SdhB), was detected in S. sclerotiorum boscalid‐resistant (BR) mutants. In the current study, replacement of the SdhB gene in a boscalid‐sensitive (BS) S. sclerotiorum strain with the mutant SdhB gene conferred resistance. Compared with wild‐type strains, BR and GSM (SdhB gene in the wild‐type strain replaced by the mutant SdhB gene) mutants were more sensitive to osmotic stress, lacked the ability to produce sclerotia and exhibited lower expression of the pac1 gene. Importantly, the point mutation was not located in the highly conserved sequence of the iron–sulfur subunit of SDH. These results suggest that resistance based on non‐conserved vs. conserved protein domains differs in mechanism. In addition to increasing our understanding of boscalid resistance in S. sclerotiorum, the new information will be useful for the development of alternative antifungal drugs. 相似文献