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31.
利用生物传感器——表面等离子共振传感器建立在活体动物中检测朊蛋白的方法,依据抗原—抗体特异性原理检测牛奶中朊蛋白。结果表明:应用表面等离子共振技术进行检测,1 h以内即可达到在缓冲液中标准最低检测限30 ng/mL的水平,牛奶样品的最低检测限是120 ng/mL。 相似文献
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AIM: To observe the mechanisms of RhoA on vascular reactivity following hemorrhagic shock (HS) in rats. METHODS: The superior mesenteric artery (SMA) in rats subjected to hemorrhagic shock was adopted to assay the vascular reactivity via observing the contraction initiated by norepinephrine (NE) with isolated organ perfusion system. Meanwhile, the effects of Rho kinase, myosin light chain phosphatase (MLCP), myosin light chain kinase (MLCK) on RhoA regulating vascular reactivity were observed. The effects of RhoA agonist U-46619 and inhibitor C3 enzyme on the activities of Rho kianse, MLCP, MLCK and phosphorylation of MLC20 in the vascular smooth muscle cells (VSMC) with hypoxia were also measured. RESULTS: As compared to control group, the cumulative dose-response curves of SMA to NE at 2 h after shock shifted to the right, the maximal contractions (Emax) of NE was significantly decreased. RhoA agonist U-46619 increased the vascular reactivity in the late period of shock. C3 enzyme abolished U-46619 induced the increase in the contractile response of SMA to NE. Rho kinase inhibitor Y-27632 decreased U-46619-induced the increase in the vascular reactivity, MLCP inhibitor calyculin further promoted the increase in the vascular reactivity. However, MLCK inhibitor had no effect on the U-46619-induced change of vascular reactivity. After hypoxia, the activities of Rho kinase and MLCK, and the level of MLC20 phosphorylation were decreased, MLCP activity was increased. RhoA agonist U-46619 increased the activity of Rho kinase and phosphorylation of MLC20, decreased the activity of MLCP, but had no effects on MLCK activity. CONCLUSION: RhoA plays an important role in the regulation of vascular reactivity following shock. The mechanism is closely related to regulating the activities of Rho kinase and MLCP, and increasing the phosphorylation of MLC20 in VSMC. 相似文献
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目的 基于无人机激光雷达(LiDAR)点云数据提取杉木树冠上部结构参数(树冠顶点、树高、冠幅和上部冠长),并进行树冠上部外轮廓模拟与可视化,为树种识别提供树木冠形特征。 方法 利用LASTools开源工具从激光雷达点云数据生成无孔洞的冠层高度模型,使用LiDAR360软件,采用局部最大值法检测树冠顶点,基于CHM种子点对点云进行单木分割,并在ArcGIS下手动选取杉木单株点云样本,用Python编程对“欠分割”样本进行单木纯化(之后全部编程方式自动化处理);提取纯化后单株样本的树冠上部结构参数(树冠顶点、树高、冠幅和上部冠长),再对单木点云按照一定高度间隔进行分层切片,使用宽度百分位数法提取单木树冠上部的相对着枝深度、枝条长度作为模型变量,以相对着枝深度分层分别建模与验证样本按照3倍标准差法剔除异常外轮廓点,选取二次多项式、幂函数和指数函数3个基础模型进行模型拟合与验证,最后采用最优拟合模型进行样地尺度的三维可视化。 结果 无人机激光雷达综合单木检测率为79.63%,结合实测参数与提取结果进行相关分析,树高线性回归R2为0.890 5,冠幅线性回归R2为0.845 6;二次抛物线、幂函数和对数函数拟合R2分别为0.807 0、0.817 0、0.806 0,幂函数对杉木树冠上部外轮廓的拟合效果更优。 结论 在高林分密度条件下,单木点云的有效提取纯化对客观描绘树冠形状非常重要;基于无人机激光雷达拟合的杉木树冠上部外轮廓反映了杉木的树冠上部形态,可为杉木的树种识别提供参考。 相似文献
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为深入了解桉树生态水文过程,正确认识桉树水文功能,本文通过野外实测法,对不同林龄尾巨桉林下穿透雨进行连续观测,并结合林外降雨量分析尾巨桉人工林林下穿透雨特征及其与降雨的关系.结果发现:尾巨桉各林龄林下穿透雨量与降雨量呈极显著正相关线性模型(P<0.01);林下穿透雨率与降雨强度呈极显著正相关(P<0.01),截留率与降雨强度呈极显著负相关(P<0.01),变异系数随降雨强度的增大先增大后减小,且两者均与降雨量无显著相关性;干湿季林下穿透雨率差异显著,湿季显著大于干季(P<0.05),最大穿透雨率及最小穿透雨率分别是干季的1.17倍和3.2倍. 相似文献
36.
XI Yu-hui MENG Qing-wei XU Chang-qing WANG Li-na LIN Yan LI Hong-zhu ZHANG Li 《园艺学报》2010,26(5):844-847
AIM: To investigate the expression and function of sirtuin 1 (Sirt1), one of the class III histone deacetylases, in hypertrophied mouse myocardium induced by isorenin (ISO). METHODS: The Kunming mice were randomly divided into 3 groups: control group, ISO group and ISO+nicotinamide (NAM) group. The myocardial hypertrophy was induced by dorsal subcutaneous injection of isorenin. Nicotinamide, an inhibitor against Sirt1, was given by peritoneal injection. Heart weight index (heart weight/body weight), hematoxylin and eosin staining, transmission electron microscope and mRNA expression of brain natriuretic peptide (BNP) were observed to identify the myocardial hypertrophy. The expression of Sirt1 in mRNA and protein levels was detected by RT-PCR and Western blotting, respectively. RESULTS: Compared to control group, the results of heart weight index, hematoxylin and eosin staining, the observation of transmission electron microscopy and mRNA expression of BNP showed that the mouse myocardial hypertrophy was induced by isorenin successfully. The Sirt1 expression was increased in hypertrophy model group (P<0.01 vs control group). Treatment with nicotinamide inhibited the cardiac hypertrophy induced by ISO (P<0.05 vs ISO group) and decreased the expression of Sirt1 (P<0.01 vs ISO group). CONCLUSION: Activation of Sirt1 might be involved in the process of myocardial hypertrophy stimulated by isorenin in mice. 相似文献
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植物衰老的分子机制及其调控 总被引:2,自引:0,他引:2
综述了植物衰老的意义和影响衰老的内部、外部因素 ,并从分子水平上探讨了植物衰老的机制及其遗传学调控 相似文献