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121.
A new technique by High Performance Liquid Chromatography (HPLC-gel permeation) shows promise as a tool to separate and quantitate the Unsaturated Vitamin B(12) Binding Capacity (UBSC) of the individual Vitamin B(12) binders in blood serum. This method, although not as rapid as protein-coated charcoal or cellulose separation techniques, is more applicable for use with large numbers of samples than gel filtration. The use of a radioactivity detector to monitor the eluant from the column permitted automation of the method. Comparable results for UBBC and for the UBBC of individual binders were obtained when samples were analyzed by gel filtration and HPLC. The HPLC method proved suitably precise and the recovery of added cyanocobalamin was acceptable. It is proposed that HPLC be the method of choice for measurement of the USBC of binders of Vitamin B(12) in blood serum.  相似文献   
122.
Various compounds and basal media were tested for their suitability to create a semi-selective medium for isolation ofClavibacter michiganensis subsp.sepedonicus (Cms) from cattle manure slurry containing c. 108 colony forming units (cfu) per ml.Plating efficiency of Cms in yeast glucose mineral medium (YGM) was 104% compared with yeast peptone glucose medium. Nalidixic acid, polymyxin B sulphate and the experimental disinfectant S-0208 inhibited colony growth of cattle slurry bacteria as compared with Cms in YGM. The optimal concentration of these inhibitors in combination was determined by modified agar diffusion tests and by pour plating in 24-well tissue culture plates. The semi-selective medium YGMI consisted of YGM supplemented with nalidixic acid (2 mg/l), polymyxin B sulphate (30 mg/l) and S-0208 (125 mg/l). Plating efficiency varied for Cms between 50.9 and 69.6%, for cattle slurry bacteria between 1.8 and 2.5% and for saprophytes from potato heel end extracts between 11.5 and 27.4%.Differentiation of Cms colonies from other colonies was based on their small and bluish colony morphology in pour plates and on immunofluorescence colony-staining (IFC). IFC of a pure culture of micro colonies of Cms in YGM was possible after one day incubation (colonies c. 5 cells). Green background fluorescence in the agar gels was prevented by addition of Tween 20 (0.1%) to the washing buffer and the use of 1% agar gels. IFC of macro colonies of Cms in YGMI, visible with 4x objective magnification, was possible after 4 days. The detection level of the target organism in artificially inoculated cattle slurry in YGMI based on colony morphology varied between 1.4×103 and 2.3×104 cfu per ml of cattle slurry. Miniaturized plating combined with IFC, using wells in tissue culture plates (=16 mm), proved suitable for detection, but was c. 30 times les sensitive. The recovery of Cms was negatively correlated with the number of saprophytic colonies in the agar plates (R 2=0.74).  相似文献   
123.
栎粉舟蛾Femtoma ocypete(Bremer)是柞树的重要害虫之一。此虫在辽宁一年发生一代,以蛹在土中越冬。翌年7月中旬开始羽化,持续到8月中旬。羽化后即可交配产卵。7月下旬到8月下旬均有幼虫孵出。幼虫经6个龄期,于9月中、下旬入土化蛹。防治方法:8月中旬往柞树上喷洒0.025%浓度的“杀虫灵”农药,能杀死各龄幼虫,防治效果为90%左右,七天后养蚕无害。  相似文献   
124.
1983~1985年以“黄壳早”、“芦竹青”、“古巴苎麻”和“武冈红皮种”为材料进行自交,并观测了自交一代的分离和变异情况,研究结果表明:a.根据自交一代的形态分类,可将“芦竹青”繁殖后代分为40个类型,“芦竹青”自交一代的麻骨颜色分离为四种,其分离比例为9.3:4.2:3:0.7,基本符合孟德尔遗传规律;b.个体间产量性状差异很大,株高变冥为0.23~1.68m,茎粗变异为0.48~1.14 cm,有效株变异为1~23株;c.40个类型的纤维细度的变异呈正态分布,变异为1168~1905公支,最细的类型和最粗的类型相差747支上述结果表明:苎麻自交后代的形态性状、产量性状和纤维细度均产生显著的分离和差异。  相似文献   
125.
对在山东的济南、平度、莱西、烟台种植的几种陆地棉(Gossypium hirsutumL.)核雄性不育材料的育性表现进行了研究,结果表明:洞A不育系的衍生材料MB、MA在不同气候条件下有育性的变化。在济南高度不育,可作为不育系。在其他几个地区表现不同程度的可育。其中MB在平度有相当好的育性,能正常结铃。而双隐性核不育材料59A、62A未能观察到育性变化。本文就核不育材料在棉花杂交制种中的应用前景及需深入研究的问题作了探讨。  相似文献   
126.
光敏核不育水稻选育与利用的几个问题讨论   总被引:4,自引:0,他引:4  
对现有光敏核不育材料进行了分类,分为4种遗传类型;其中,温光弱感到光敏核不育系是最为理 想的遗传工具,并就其选育途径和选择“粳不籼恢”繁殖制种技术体系进行了论证.  相似文献   
127.
“复激保果剂”在杂交水稻制种上应用技术总结   总被引:1,自引:0,他引:1  
文英 《杂交水稻》1993,(2):19-21
复激保累剂,在杂交稻制种上使用,能促使花器发育良好,调节父母本花期,提高结实率,增加每穗实粒和粒重,提高产量。且成本低,有显著的经济效益。  相似文献   
128.
The electrokinetic properties of feline blood lymphocytes isolated by centrifugation over Ficoll-Isopaque gradient were investigated. A biphasic electrophoretic mobility (EPM) distribution was regularly observed with a low-mobility (LM) population (mean EPM: 0.82) accounting for 32% of blood lymphocytes and a high-mobility (HM) population (mean EPM: 1.09) representing 68% of blood lymphocytes. Following fractionation on nylon-wool columns, lymphocytes with B-cell properties (64% sIg+; 9% guinea pig erythrocytes (GPE)-rosette+, PHA and Con A unresponsive) were enriched in the adherent fraction and belonged mainly (78%) to the LM population. In contrast, lymphocytes with T properties (5% sIg+, 42% GPE-rosette+, PHA and Con A responsive) were recovered in the effluent fraction and comprised 84% of HM elements.Thus, in cat blood, LM lymphocytes are likely to represent in majority B cells and HM lymphocytes T cells. This indicates that cell electrophoresis provides an interesting mean for differentiating B and T cells in the cat.  相似文献   
129.
130.
The construction and application is described of a polystyrol humidity box in which wheat leaves, while continuing to function as parts of living plants, can be tested for their reactions toSeptoria spp. in an atmosphere nearly saturated with water, as is required for successful infection. The method is simple, accurate ans inexpensive.Samenvatting Voor dit doel is een z.g. vochtdoos geconstrueerd (Fig. 1A). Het te toetsen blad wordt daar doorheen geleid en in de doos geïnoculeerd met een druppel conidiën-suspensie van de schimmel. Onder het blad staat wat water in de doos (Fig. 1B). Na afsluiting ontstaat in de doos de hoge luchtvochtigheid van bijna 100% die nodig is voor de infectie. Dit wordt op deze wijze eenvoudig en goedkoop gerealiseerd. De bladeren die zo worden getoetst blijven onbeschadigd functioneren aan de plant. Na enkele dagen kan de doos worden geopend en kan de symptoom-ontwikkeling worden afgewacht en gevolgd (Fig. 3A, 3B en 4). De methode leent zich voor nauwkeurig werk en vereist zeer weinig infectiemateriaal. De Technische en Fysische Dienst voor de Landbouw (TFDL), Wageningen, ontwierp en construeerde een statief voor het gebruik van de vochtdozen in serie (Fig. 2).  相似文献   
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