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41.
将步长加速法与混沌优化方法结合,解决了混沌优化方法收敛速度慢和步长加速法只适合于局部寻优的缺陷.为此,介绍了无糖组培营养液循环控制系统的设计和构成,并采用混沌-步长加速法针对无糖组培营养液控制系统的PID控制器参数寻优,以实现营养液的自动调配.仿真结果表明:该优化方法搜索效率高,所得参数较好地满足了系统控制要求. 相似文献
42.
棉田膜内与膜间土壤溶液含盐量的变化 总被引:1,自引:0,他引:1
用定期取表层土样测定其电导率和在不同深度埋设盐分传感器探头的方法 ,在作物生长季节内 ,监测了棉田膜内和膜间不同深度的土壤溶液含盐量变化。结果为 :1棉田膜内与膜间表层土壤和 1 0 cm、30 cm深土壤溶液含盐量变化较大 ,且规律相同。未灌水时上升 ,灌水后迅速下降。膜间未灌水期间的含盐量上升幅度大于膜内 ,灌水对膜内和膜间表土洗盐、1 0 cm、30 cm深土壤溶液含盐量的降低作用没有差别。降雨可引起膜内和膜间 1 0 cm深土壤溶液电导率的变化 ,这个影响也是膜间大于膜内。 2 60 cm深的土壤溶液不存在明显的盐分累积现象 ,灌水可使这里的土壤溶液含盐量缓慢降低 ,膜间的降低过程快于膜内 相似文献
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标准溶液的不确定度对农药残留检测起着非常重要的作用,影响着检测结果的准确性。笔者以实际应用的14种有机磷农药混合标准溶液为例,采用配制混合标准溶液过程单元操作的不确定度计算方法(top down),分析了在配制混合标准溶液过程中的所有影响因素,得到了最终的扩展不确定度。最终结果显示使用精准的移液器将储备液配置为混合标液,得到最终的扩展不确定度相对小。 相似文献
46.
C. M. Geraldson 《Journal of plant nutrition》2013,36(8):1091-1098
The concentration and balance of nutrients in both the hydroponic or soil solution has been evaluated with relevance to tomato productivity. Yields of 200 mt/ha have been produced in greenhouse, hydroponic culture in a 9 to 10 month period. Yields of more than 100 mt/ha of field grown tomatoes have been produced in Florida in a 4 to 5 month period. Within the limitations of either culture, it is possible per unit of time to provide the nutrients required to produce equivalent yields. It is most significant that field grown tomatoes in Florida can be grown with minimal management and at a fraction of the cost of those grown hydroponically. The validity of the Florida fresh market tomato industry is based on the production efficiency of the field culture. There are annually 16,000 ha of tomatoes grown in Florida, perhaps less than 40 ha grown in hydroponic cultures. 相似文献
47.
方聪娜 《厦门水产学院学报》2012,(4):297-300
利用指数型二分性理论及相关分析技巧,研究了一类具有有限时滞的非算子型的中立型泛函微分方程的概周期解问题,得到了方程存在唯一稳定的概周期解的新结果. 相似文献
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以滞量τ为分支参数,研究了具时滞的能源价格模型的动力学行为,这些行为包括:系统在平衡点附近的稳定性,局部Hopf分支的存在性,发生条件Hopf分支的方向,分支周期解的稳定性以及分支随参数变化其周期解的周期变化.最后通过数值模拟验证了理论分析结果,并用分支理论解释了能源价格模型产生且维持周期振荡的原因. 相似文献
50.
《Communications in Soil Science and Plant Analysis》2012,43(5):483-495
Abstract When sugarbeet seedlings are transferred from a complete nutrient solution to one from which Ca has been withheld, the rootlets and tops fail to develop. The same transfer at the eight‐leaf stage causes the rootlets to become stubby and swollen at the tips and blade expansion becomes modified; particularly the upper portions of the blades attaining nearly full development, which pucker and often develop a cupping or hooding effect; a unique symptom characteristic of Ca deficiency. As each new leaf develops, the blade area becomes smaller until only a black tip remains at the apex of the petiole, which is the symptom referred to as tip‐burn for this petiole and the successively . shorter petioles formed as Ca deficiency increases in severity. Strangely, these symptoms also appear during periods of rapid growth when the nutrient solution contains as much as 10 to 28 milliequivalents per liter of Ca or when soils are high in Ca. This implies that Ca absorption and possibly translocation limits the Ca supply at the growing point. Increasing Mg in the nutrient solution decreases Ca uptake and increases Ca deficiency. Potassium deficiency, unexpectedly, induces Ca deficiency apparently by decreasing the translocation of Ca to the growing point. These phenomena suggest the hypothesis that when ion absorption takes place from the root exchange site that has the affinity for H > Ca > Mg > K > Na, then the H generated internally replaces, and the roots absorb, Na, K and Mg preferentially. Externally, Ca would be adsorbed preferentially from the nutrient solution by the exchange complex, and with the addition of Mg, it would compete for the common adsorption site of Ca and limit Ca absorption internally. Under these conditions potassium‐deficient nutrient solutions would not induce Ca deficiency by decreasing Ca absorption but rather by decreasing Ca translocation. Theoretically, Ba would replace H more readily than Ca on the exchange complex, and therefore, Ba would be adsorbed preferentially and Ca uptake would increase. This effect of Ba was verified experimentally. Since the translocation of 45Ca to the growing point was found to be unrestricted under Ca‐sufficient and Ca‐deficient conditions and since the formation of insoluble Ca compounds such as phosphate or oxalate did not account for the Ca deficiency at the growing point, the cause of the Ca deficiency at the growing point is most likely the higher priority of the storage root for Ca over tops when leaf blades and storage root are both expanding rapidly. However, Ca retransport from older to younger parts of the sugarbeet plant may be restricted by the formation of Ca phosphate under Ca‐deficient conditions and Ca oxalate under Ca‐sufficient conditions. Calcium deficiency increases net photosynthesis per unit blade area initially, probably because of blade puckering, but not on a per unit chlorophyll basis. 相似文献