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1.
BackgroundASF was first reported in Kenya in 1910 in 1921. In China, ASF spread to 31 provinces including Henan and Jiangsu within six months after it was first reported on August 3, 2018. The epidemic almost affected the whole China, causing direct economic losses of tens of billions of yuan. Cause great loss to our pig industry. As ELISA is cheap and easy to operate, OIE regards it as the preferred serological method for ASF detection. P54 protein has good antigenicity and is an ideal antigen for detection.ObjectiveTo identify a conservative site in the African swine fever virus (ASFV) p54 protein and perform a Cloth-enzyme-linked immunosorbent assay (ELISA) for detecting the ASFV antibody in order to reduce risks posed by using the live virus in diagnostic assays.MethodWe used bioinformatics methods to predict the antigen epitope of the ASFV p54 protein in combination with the antigenic index and artificially synthesized the predicted antigen epitope peptides. Using ASFV-positive serum and specific monoclonal antibodies (mAbs), we performed indirect ELISA and blocking ELISA to verify the immunological properties of the predicted epitope polypeptide.ResultsThe results of our prediction revealed that the possible antigen epitope regions were A23–29, A36–45, A72–94, A114–120, A124–130, and A137–150. The indirect ELISA showed that the peptides A23–29, A36–45, A72–94, A114–120, and A137–150 have good antigenicity. Moreover, the A36–45 polypeptide can react specifically with the mAb secreted by hybridoma cells, and its binding site contains a minimum number of essential amino acids in the sequence 37DIQFINPY44.ConclusionsOur study confirmed a conservative antigenic site in the ASFV p54 protein and its amino acid sequence. A competitive ELISA method for detecting ASFV antibodies was established based on recombinant p54 and matching mAb. Moreover, testing the protein sequence alignment verified that the method can theoretically detect antibodies produced by pigs affected by nearly all ASFVs worldwide.  相似文献   
2.
基于粒子群算法的圆柱度误差评定方法   总被引:5,自引:0,他引:5  
根据最小区域条件,建立了圆柱度误差的数学模型以及优化目标函数和适应度函数,阐述了粒子群优化算法的原理和实现方法,然后根据粒子群算法优化求解。实例表明,该方法对于圆柱度误差评定等非线性优化问题能得到全局最优解,粒子群优化算法的计算精度与其他满足最小条件的计算方法相比略有提高,且参数设置少,计算速度快,可用于三坐标测量机等测量系统的圆柱度误差测量后的数据处理。  相似文献   
3.
基于纹理和位置特征的麦田杂草识别方法   总被引:19,自引:5,他引:14  
以化学防除适期麦田杂草为研究对象,对利用条播作物的位置和纹理特征识别田间杂草的方法进行了研究。根据条播作物小麦作物行的间距相对固定等位置特征,利用植物像素直方图法确定作物行的中心线和行宽,并识别行间杂草。然后,以作物行中心为基准来选取纹理块,计算量化级数为8级的H颜色空间的共生矩阵,提取5个纹理特征参数,利用K均值聚类法判别分析各块的类别来识别行内杂草。研究结果表明,杂草的正确识别率约为93%,作物的错误识别率约为7%。  相似文献   
4.
Fucosylated chondroitin sulfates (FCSs) FCS-BA and FCS-HS, as well as fucan sulfates (FSs) FS-BA-AT and FS-HS-AT were isolated from the sea cucumbers Bohadschia argus and Holothuria (Theelothuria) spinifera, respectively. Purification of the polysaccharides was carried out by anion-exchange chromatography on DEAE-Sephacel column. Structural characterization of polysaccharides was performed in terms of monosaccharide and sulfate content, as well as using a series of non-destructive NMR spectroscopic methods. Both FCSs were shown to contain a chondroitin core [→3)-β-d-GalNAc-(1→4)-β-d-GlcA-(1→]n bearing sulfated fucosyl branches at O-3 of every GlcA residue in the chain. These fucosyl residues were different in pattern of sulfation: FCS-BA contained Fuc2S4S, Fuc3S4S and Fuc4S at a ratio of 1:8:2, while FCS-HS contained these residues at a ratio of 2:2:1. Polysaccharides differed also in content of GalNAc4S6S and GalNAc4S units, the ratios being 14:1 for FCS-BA and 4:1 for FCS-HS. Both FCSs demonstrated significant anticoagulant activity in clotting time assay and potentiated inhibition of thrombin, but not of factor Xa. FS-BA-AT was shown to be a regular linear polymer of 4-linked α-L-fucopyranose 3-sulfate, the structure being confirmed by NMR spectra of desulfated polysaccharide. In spite of considerable sulfate content, FS-BA-AT was practically devoid of anticoagulant activity. FS-HS-AT cannot be purified completely from contamination of some FCS. Its structure was tentatively represented as a mixture of chains identical with FS-BA-AT and other chains built up of randomly sulfated alternating 4- and 3-linked α-L-fucopyranose residues.  相似文献   
5.
1993年全国小麦秆锈菌种群动态分析   总被引:4,自引:1,他引:4  
1993年我国小麦秆锈病发生较轻,从8个省18个区县中的47个品种上采集到的95个标样中分离到菌株336个,鉴定出21C3CKR、21C3CKH、21C3CTR、21C3CTH、21C3CFR、21C3CFH、34C1MKR、34C1MKH和34C2MKR等9个致病类型;21C3CKR的出现频率为65.2%,居于首位,21C3CDH为14.5%,21C3CTR为10.7%,21C3CFR为4.2%  相似文献   
6.
土壤熏蒸剂研究进展   总被引:9,自引:3,他引:9  
土壤熏蒸剂可有效防治土传病虫害,但效果最好的熏蒸剂溴甲烷由于破坏臭氧层,已被禁止用在农业上(必要用途豁免除外)。碘甲烷、氯化苦、异硫氰酸甲酯、1,3-二氯丙烯、二甲基二硫、硫酰氟、棉隆及威百亩是国际上已经登记使用的土壤熏蒸剂;甲酸乙酯、乙二腈、糠醛、丙烯醛是有希望开发为新的土壤熏蒸剂品种。国内已经商品化的土壤熏蒸剂品种有4种,分别为氯化苦、威百亩、棉隆和硫酰氟,二甲基二硫正在登记当中。本文系统综述了上述熏蒸剂在应用、环境行为等方面的研究进展,在未来一段时间内,氯化苦、棉隆及威百亩将会占据着国内土壤熏蒸剂的主要市场。二甲基二硫的登记也将会改善国内熏蒸剂品种匮乏的局面。  相似文献   
7.
4种药剂对豇豆根结线虫病的防治效果   总被引:2,自引:0,他引:2  
为了更好地防治豇豆根结线虫病,对4种杀线虫剂进行了田间防效评价试验。结果表明,供试的4种药剂均对豇豆根结线虫有一定的防效,能控制土壤中2龄幼虫的数量和抑制根结的形成,其中10%噻唑膦颗粒剂对豇豆根结线虫的防效最好,具有低残留、持效期长等优点,可作为防治豇豆根结线虫的首选药剂; 其次为5%阿维菌素颗粒剂。同时供试的4种药剂在试验剂量范围内均对豇豆安全,建议在生产上推广应用10%噻唑膦颗粒剂和5%阿维菌素颗粒剂来防治豇豆根结线虫病。  相似文献   
8.
植原体基因组学研究进展   总被引:2,自引:0,他引:2  
植原体(phytoplasma)是一类重要的植物病原细菌, 可经叶蝉、飞虱等昆虫介体传播, 感染1 000多种植物, 产生丛枝、黄化、韧皮部黑斑坏死等症状, 给农业、林业生产带来巨大的损失。本文对植原体基因组学研究的历史、现状及当前植原体效应蛋白等方面的研究进展进行了综述。  相似文献   
9.
为探讨无机盐和有机盐对南方根结线虫的作用方式,在室内利用沙柱法和染色法测定了二者对南方根结线虫2龄幼虫迁移能力及侵入番茄根部能力的影响。结果表明,随着各盐处理浓度的增加,南方根结线虫2龄幼虫的迁移能力和侵入能力显著降低。在4μg/m L KSCN、C6H8O7、KCl、KH2PO4、KHCO3和Mn SO4·H2O沙柱中,15 d后2龄幼虫的平均迁移距离最小,分别为0、0.33、0.52、0.53、0.55和0.58 cm,而对照为0.94 cm。2龄幼虫在Ba NO3、K2HPO4、KHCO3、Cs Cl和KSCN各浓度沙柱中的平均迁移距离均小于0.94 cm。2μg/m L NH4NO3、KH2PO4、(NH4)2CO3、Cs Cl、(NH4)2SO4、Na SCN和NH4SCN处理15 d后,2龄幼虫对番茄根部的侵入率最低,分别为1%、2.33%、1.33%、2%、2%、1%和1.67%。表明对2龄幼虫侵入番茄根部抑制效果最明显的盐为NH4NO3、KH2PO4、(NH4)2CO3、Cs Cl、(NH4)2SO4、Na SCN和NH4SCN。  相似文献   
10.
Summary

Retrotransposons are major components of the genomes of most eukaryotic organisms and have resulted in the introduction of desirable traits in many crops, including fruit trees. Here, we describe a Ty3-gypsy-like retrotransposon associated with a short-catkin mutant in Chinese chestnut (Castanea mollissima), resulting in catkins that are < 20% the length of normal staminate catkins. A partial sequence of the retrotransposon, named CmRT1, detected by amplified fragment length polymorphism (AFLP) analysis, and its complete sequence were determined from the genome of Chinese chestnut (Castanea mollissima) using improved Tail-PCR. CmRT1 was 10,067 bp in length and shared high homology in its predicted amino acid sequence and motifs with other Ty3/gypsy-like retrotransposons. The 5’ long terminal repeat (LTR) of CmRT1 contained a TATA box and several cis-elements that were predicted to be important for processes involving abscisic acid, gibberellic acid, and auxins and in stress-mediated responses. Further characterisation of the transposition event that led to the short-catkin phenotype was performed using two pairs of primers that aligned with the flanking region of the LTRs. The expected PCR bands were observed only in genomic DNA from plants that showed the mutation. Finally, cloning and real-time qPCR analysis of an NADP-dependent alkenal double-bond reductase (CmADBR) target gene that was adjacent to CmRT1, revealed that CmADBR expression was significantly down-regulated in the short-catkin mutant. Taken together, these results suggest that the CmRT1 retrotransposon is responsible for the short-catkin phenotype.  相似文献   
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