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马铃薯晚疫病菌(Phytophthora infestans)能侵染多种茄科植物,它引起的马铃薯晚疫病,是马铃薯生产中的第一大病害。为了开发能在田间快速检测马铃薯晚疫病病原的方法,利用P. infestans T30-4基因组测序数据的contig 1.18131,设计qPCR和LAMP引物,优化扩增条件后得到引物的特异性和灵敏度,最后通过检测田间收获薯块,比较形态学传统方法、qPCR及LAMP的差异。特异性检测结果发现,qPCR和LAMP仅在含有P. infestans DNA模板的体系有阳性扩增,在寄主和其他微生物DNA中均无扩增;在优化的条件下,qPCR和LAMP的检测下限可达1×10 -6ng/μL,在有寄主和其他微生物DNA存在的条件下,引物的灵敏度没有显著差异。利用两种快速方法对在大理、丽江及昆明3个地区田间收获薯块上检测发现,qPCR和LAMP方法得到的检出率差异极为不显著(P=0.420),两种快速检测方法和形态学鉴定方法检出率差异极显著(P=0.009)。在大理、丽江及昆明3个地区的薯块中,两种分子检测方法检出率均比形态学方法高。其中,qPCR检测方法比形态学方法分别提高了12.00%、2.00%、8.70%;LAMP检测方法比形态学方法分别提高了11.30%、2.00%、8.70%。 相似文献
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Impact of grassland contract policy on soil organic carbon losses from alpine grassland on the Qinghai–Tibetan Plateau 下载免费PDF全文
J. Cao Y. Gong E. T. Yeh N. M. Holden J. F. Adamowski R. C. Deo M. Liu J. Zhou J. Zhang W. Zhang S. Zhang D. Sheng S. Yang X. Xu M. Li Q. Feng 《Soil Use and Management》2017,33(4):663-671
Carbon storage in the soils on the Qinghai–Tibetan Plateau plays a very important role in the global carbon budget. In the 1990s, a policy of contracting collective grasslands to smaller units was implemented, resulting in a change from the traditional collective grassland management to two new management patterns: a multi‐household management pattern (MMP: grassland shared by several households without enclosures) and a single‐household management pattern (SMP: grassland enclosed and used by only one household). In 2016, 50 MMP and 54 SMP winter pastures on the Qinghai–Tibetan Plateau were sampled to assess the differences in soil organic carbon (SOC) between the two management patterns. Results showed that average SOC was significantly greater under MMP than under SMP, with an estimated 0.41 Mg C/ha/yr lost due to SMP following the new grassland contract. Based on the government's grassland policy, four grassland utilization scenarios were developed for both summer and winter pastures. We found that if the grassland were managed under SMP, likely C losses ranged between 0.31 × 107 and 6.15 × 107 Mg C/yr across the Qinghai–Tibetan Plateau relative to MMP, which more closely resembles pre‐1990s grassland management. Previous estimates of C losses have only considered land use change (with cover change) and ignored the impacts driven by land management pattern changes (without cover change). The new data suggest that C losses from the Qinghai–Tibetan Plateau are greater than previously estimated, and therefore that the grassland contract policy should be reviewed and SMP households should be encouraged to reunite into the MMP. These findings have potential implications for land management strategies not only on the Qinghai–Tibetan Plateau but also other grazing regions globally where such practices may exist. 相似文献
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Peirong Li Tongbing Su Huiping Wang Xiuyun Zhao Weihong Wang Yangjun Yu Deshuang Zhang Changlong Wen Shuancang Yu Fenglan Zhang 《Plant Breeding》2019,138(3):309-324
Single‐nucleotide polymorphisms (SNPs) are rapid, economical and reliable genotyping tools. Non‐heading Chinese cabbage (Brassica rapa L. subsp. chinensis Makino) is now an economically important vegetable crop worldwide. In this study, 1,167 SNPs were evaluated for 7polymorphism among 70 representative non‐heading Chinese cabbage inbred lines using a Kompetitive Allele Specific PCR (KASP) genotyping assay. On the basis of identified polymorphisms and the results of a principal component analysis, we selected 50 core SNPs that were balanced sufficiently to provide adequate information for genetic identification. The core SNPs were used for construction of a neighbour‐joining dendrogram that separated the 70 inbred lines into four main groups and several subgroups corresponding to Caixin, Heiyebaicai, Huangxinwu, Naibaicai, Taitsai, Pak‐choi, and Wutatsai. This categorization was superior to that achieved using a dataset of 479 polymorphic SNPs. To confirm the utility of the core SNP markers in genetic identification, we tested their stability and resolution using 162 commercial hybrid cultivars. The SNPs, which represent a cost‐effective, accurate marker set for germplasm analysis and cultivar identification, are suitable for molecular marker‐assisted breeding in non‐heading Chinese cabbage. 相似文献
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用两株单克隆抗体混合后包被ELLISA微孔板,加牛冠状病毒抗原,加经白陶土处理过的兔抗牛冠状病毒免血清,再加上辣根氧化物酶标记的羊抗兔IgG抗体,加底物质显色间接ELISA检测牛冠状病毒抗原获得成功。用此方法检测细胞培养的牛冠状病毒上清液,其敏感度高出血凝试验(HA)8倍,从武汉市附近3个奶牛场采集犊牛腹泻粪便105份,用单抗ELISA检测牛冠状病毒抗原,共检出阳性36份,并与血凝及血凝抑制试验, 相似文献
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鸡白介素18基因原核表达质粒构建 总被引:7,自引:0,他引:7
根据已发表的江西土鸡白介素 -1 8(Ch IL-1 8) c DNA编码基因序列设计引物 ,用PCR技术从 p MDCh IL-1 8质粒扩增出编码鸡IL-1 8成熟蛋白基因 ,重组于 p BV2 2 0表达载体上 ,将重组质粒转化大肠杆菌 JM1 0 9(DE3 ) ,转化子经温度诱导的表达产物 ,SDS-PAGE电泳鉴定约 2万 ,N端开头 1 5个氨基酸序列测定分析 ,证明获得了鸡 IL-1 8成熟蛋白 ,为今后深入研究鸡 IL -1 8的生物学特性及其临床应用打下了基础 相似文献