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21.
The present study was to investigate the feasibility and efficiency of the DNA vaccine to protect chickens against very virulent infectious bursal disease virus (vvIBDV) infection. A plasmid DNA carrying VP2‐4‐3 genes of vvIBDV SH95 and a plasmid DNA carrying chicken interleukin‐6 (ChIL‐6) genes were constructed and designated as pALTER‐MAX‐VP2‐4‐3 and pALTER‐MAX‐ChIL‐6 respectively. Several DNA vaccination experiments were performed: 1‐week‐old chickens were intramuscularly injected with only plasmid pcDNA3‐VP2, pALTER‐MAX‐VP2‐4‐3 or mixture with pALTER‐MAX‐ChIL‐6. The chickens at 4 weeks old were orally inoculated with vvIBDV SH95. The results showed that immunization with the mixture of pALTER‐MAX‐VP2‐4‐3 and pALTER‐MAX‐ChIL‐6 three times conferred protection for 90% of chickens. Enzyme‐linked immunosorbent assay (ELISA) antibody titres in chickens immunized together with pALTER‐MAX‐ChIL‐6 were higher than those immunized simply with plasmid pcDNA3‐VP2 or pALTER‐MAX‐VP2‐4‐3. IBDV was not detected in the bursa of the protected chickens at 8 days after challenge by RT‐PCR. The results indicate that protection against vvIBDV can be achieved by using the VP2‐4‐3 gene of vvIBDV as a DNA vaccine. Furthermore, the simultaneous injection of ChIL‐6 plasmid significantly increased the protection after challenge with the very virulent strain.  相似文献   
22.
‘三棱榄''橄榄果实香气成分分析   总被引:7,自引:1,他引:7  
1 材料与方法选取广东优良鲜食橄榄品种‘三棱榄’,2001年12月6日采样,采用固相微萃取法(SPME)富集香气成分(鲜橄榄果肉于15℃下捣碎后取样1.0 g放入4 mL聚四氟乙烯硅橡胶垫密封螺口玻璃瓶中,插入100μm聚二甲基硅氧烷纤维头于室温25-30℃顶空取样2 h),用美国Finnigan TRACE GC-MS气相色谱-质谱联用仪进行分析。气相色谱柱为DB-1弹性毛细管柱30 m×0.25 mm,载气为He(99.99%),流速1.0mL/min。程序升温从40℃开始先保持10 min,后以2℃/min的升温速率升至150℃保持10 min。质谱条件:电子能量70 eV,离子源温度250℃,质量范围35-450 aum,不分流进样。2002年12月18日采样重复分析。  相似文献   
23.
SeGLP-1的分离纯化及硒活性结构分析   总被引:8,自引:0,他引:8  
灵芝(Ganoderma lucidum)加硒深层培养后的菌丝(含Se1600μg/g)分别经水及碱水提取,醇析,透析,Sevage法脱蛋白,DEAE-cellulose柱层析纯化,得SeGLP-1。经SephadexG-100,聚丙烯酰胺凝胶电泳和紫外光谱分析鉴定,SeGLP-1为均一级分。GC与TLC分析表明,SeGLP-1含Gal,Glu,Xyl,Rha,Man,其单糖摩尔比为Gal:Glu:Xyl:Rha:Man=0.23:1.00:0.72:0.25:0.09。SeGLP-1硒含量1642μg/g。SeGLP-1中Se活性中心的结构可能为O=Se=O,即Se取代了灵芝多糖GLP-1中-OCH3结构上的CH3,从而形成了硒氧双键结构。  相似文献   
24.
25.
Ascospores of both A-group and B-group Leptosphaeria maculans germinated at temperatures from 5 to 20°C on leaves of oilseed rape. Germination of ascospores of both groups started 2 h after inoculation and percentage germination reached its maximum about 14 h after inoculation at all temperatures. Both the percentage of A-/B-group ascospores that had germinated after 24 h incubation and germ tube length increased with increasing temperature from 5 to 20°C. Germ tubes from B-group ascospores were longer than those from A-group ascospores at all temperatures, with the greatest difference at 20°C. Hyphae from ascospores of both groups penetrated the leaves predominantly through stomata, at temperatures from 5 to 20°C. A-group ascospores produced highly branched hyphae that grew tortuously, whereas B-group ascospores produced long, straight hyphae. The percentage of germinated ascospores that penetrated stomata increased with increasing temperature from 5 to 20°C and was greater for A-group than for B-group L. maculans after 40 h incubation.  相似文献   
26.
An epidemic is the progress of disease in time and space. Each epidemic has a structure whose temporal dynamics and spatial patterns are jointly determined by the pathosystem characteristics and environmental conditions. One of the important objectives in epidemiology is to understand such spatio-temporal dynamics via mathematical and statistical modelling. In this paper, we outline common methodologies that are used to quantify and model spatio-temporal dynamics of plant diseases, with emphasis on developing temporal forecast models and on quantifying spatial patterns. Several examples of epidemiological models in cereal crops are described, including one for Fusarium head blight.  相似文献   
27.
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   
28.
熊蜂为温室茄子授粉试验   总被引:12,自引:1,他引:12  
通过对温室茄子应用熊蜂授粉、人工蘸花授粉和空白对照的比较研究,结果表明熊蜂组的座果数比人工组和对照组分别增加了17.84%和33.32%,产量比人工组和对照组分别提高了27.93%和41.98%,果实含糖量比人工组和对照组分别增加了18.33%和21.16%,而且,熊蜂组的果实大而充实,商品性较好.说明利用熊蜂为温室茄子授粉,不仅能够促进座果,提高产量,而且可以改善果实品质,提升产品的附加值.  相似文献   
29.
以川梨、砂梨、豆梨和杜梨为材料,研究了在缺铁胁迫下培养介质的pH值和根系Fe3+还原酶活性的变化。结果表明,缺铁胁迫使4种砧木的介质pH值于处理的第2天就迅速降低,并且一直低于低铁和正常供铁处理;而低铁处理下,介质pH值在最初几天内反而高于正常处理,至4~5d之后才逐渐低于正常供铁处理;同时,NH4+-N对降低介质pH值和缓解缺铁症状有利。4种砧木的根系Fe3+还原酶活性都随供铁浓度的增加而不同程度的增大:无铁处理下,砂梨根系Fe3+的还原能力最小、杜梨最大;而在低铁和正常供铁条件下,砂梨和川梨的还原能力最强,杜梨次之,豆梨最小。还原酶大小与症状表现之间具有一致性。  相似文献   
30.
SUN Fen-yong  PAN Qiu-hui  HONG An 《园艺学报》2004,20(12):2316-2319
AIM: To further investigate the role of PKARⅠβ in the growth-promoting effects of shuang long Jiegu pill (SLJGP), a Chinese medicine, on cultured osteoblasts. METHODS: pcDNA- antiPKARⅠβ, a recombinant expressing the antisense sequence of PKARⅠβ, was constructed and transformed HFOB1.19 by lipofectin. MTT was undertaken to assess the cell growth with the treatment of high dosage of SLJGP containing serum. RESULTS: Antisense gene blocked the growth-promoting effects of SLJGP containing serum on HFOB1.19. CONCLUSION: The function of SLJGP is closely related to cAMP-dependent protein kinase A.  相似文献   
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